Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| geneid | 23168 |
|---|---|
| ensemblid | ENSG00000137815.15 |
| hgncid | 28996 |
| symbol | RTF1 |
| name | RTF1 homolog, Paf1/RNA polymerase II complex component |
| refseq_nuc | NM_015138.5 |
| refseq_prot | NP_055953.3 |
| ensembl_nuc | ENST00000389629.9 |
| ensembl_prot | ENSP00000374280.4 |
| mane_status | MANE Select |
| chr | chr15 |
| start | 41417095 |
| end | 41483563 |
| strand | + |
| ver | v1.2 |
| region | chr15:41417095-41483563 |
| region5000 | chr15:41412095-41488563 |
| regionname0 | RTF1_chr15_41417095_41483563 |
| regionname5000 | RTF1_chr15_41412095_41488563 |
| 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 | 710 | 225 | 54 | 48 | 73 | 14 | 34 | 55 | RTF1_chr15_41412095_41488563 | RTF1 | copy fasta | chr15 | 41412095 | 41488563 |
| a0002 | 0/0 | 710 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | RTF1_chr15_41412095_41488563 | RTF1 | copy fasta | chr15 | 41412095 | 41488563 |
| 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 | 2133 | 219 | 52 | 48 | 72 | 13 | 32 | RTF1_chr15_41412095_41488563 | RTF1 | copy fasta | chr15 | 41412095 | 41488563 |
| c0002 | 0/0 | 2133 | 2 | 2 | 0 | 0 | 0 | 0 | RTF1_chr15_41412095_41488563 | RTF1 | copy fasta | chr15 | 41412095 | 41488563 |
| c0003 | 0/0 | 2133 | 1 | 0 | 0 | 0 | 1 | 0 | RTF1_chr15_41412095_41488563 | RTF1 | copy fasta | chr15 | 41412095 | 41488563 |
| c0004 | 0/0 | 2133 | 1 | 0 | 0 | 1 | 0 | 0 | RTF1_chr15_41412095_41488563 | RTF1 | copy fasta | chr15 | 41412095 | 41488563 |
| c0005 | 0/0 | 2133 | 1 | 0 | 0 | 0 | 0 | 1 | RTF1_chr15_41412095_41488563 | RTF1 | copy fasta | chr15 | 41412095 | 41488563 |
| c0006 | 0/0 | 2133 | 1 | 0 | 0 | 0 | 0 | 1 | RTF1_chr15_41412095_41488563 | RTF1 | copy fasta | chr15 | 41412095 | 41488563 |
| c0007 | 0/0 | 2133 | 1 | 0 | 0 | 1 | 0 | 0 | RTF1_chr15_41412095_41488563 | RTF1 | copy fasta | chr15 | 41412095 | 41488563 |
| thapid | grch38chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| t0001 | 0/1 | 2898 | 59 | 15 | 13 | 24 | 1 | 5 | RTF1_chr15_41412095_41488563 | RTF1 | copy fasta | chr15 | 41412095 | 41488563 |
| t0002 | 1/0 | 2898 | 33 | 1 | 6 | 17 | 4 | 4 | RTF1_chr15_41412095_41488563 | RTF1 | copy fasta | chr15 | 41412095 | 41488563 |
| t0003 | 0/0 | 2896 | 26 | 7 | 10 | 1 | 5 | 3 | RTF1_chr15_41412095_41488563 | RTF1 | copy fasta | chr15 | 41412095 | 41488563 |
| t0004 | 0/0 | 2896 | 23 | 1 | 6 | 14 | 1 | 1 | RTF1_chr15_41412095_41488563 | RTF1 | copy fasta | chr15 | 41412095 | 41488563 |
| t0005 | 0/0 | 2895 | 15 | 6 | 4 | 0 | 2 | 3 | RTF1_chr15_41412095_41488563 | RTF1 | copy fasta | chr15 | 41412095 | 41488563 |
| t0006 | 0/0 | 2897 | 11 | 0 | 3 | 4 | 0 | 4 | RTF1_chr15_41412095_41488563 | RTF1 | copy fasta | chr15 | 41412095 | 41488563 |
| t0007 | 0/0 | 2899 | 10 | 2 | 1 | 2 | 0 | 5 | RTF1_chr15_41412095_41488563 | RTF1 | copy fasta | chr15 | 41412095 | 41488563 |
| t0008 | 0/0 | 2899 | 7 | 0 | 0 | 3 | 1 | 3 | RTF1_chr15_41412095_41488563 | RTF1 | copy fasta | chr15 | 41412095 | 41488563 |
| t0009 | 0/0 | 2897 | 7 | 4 | 2 | 1 | 0 | 0 | RTF1_chr15_41412095_41488563 | RTF1 | copy fasta | chr15 | 41412095 | 41488563 |
| t0010 | 0/0 | 2898 | 4 | 4 | 0 | 0 | 0 | 0 | RTF1_chr15_41412095_41488563 | RTF1 | copy fasta | chr15 | 41412095 | 41488563 |
| t0011 | 0/0 | 2896 | 4 | 3 | 1 | 0 | 0 | 0 | RTF1_chr15_41412095_41488563 | RTF1 | copy fasta | chr15 | 41412095 | 41488563 |
| t0012 | 0/0 | 2896 | 3 | 3 | 0 | 0 | 0 | 0 | RTF1_chr15_41412095_41488563 | RTF1 | copy fasta | chr15 | 41412095 | 41488563 |
| t0013 | 0/0 | 2896 | 3 | 0 | 0 | 3 | 0 | 0 | RTF1_chr15_41412095_41488563 | RTF1 | copy fasta | chr15 | 41412095 | 41488563 |
| t0014 | 0/0 | 2896 | 2 | 2 | 0 | 0 | 0 | 0 | RTF1_chr15_41412095_41488563 | RTF1 | copy fasta | chr15 | 41412095 | 41488563 |
| t0015 | 0/0 | 2898 | 2 | 2 | 0 | 0 | 0 | 0 | RTF1_chr15_41412095_41488563 | RTF1 | copy fasta | chr15 | 41412095 | 41488563 |
| t0016 | 0/0 | 2897 | 2 | 0 | 1 | 0 | 0 | 1 | RTF1_chr15_41412095_41488563 | RTF1 | copy fasta | chr15 | 41412095 | 41488563 |
| t0017 | 0/0 | 2896 | 2 | 0 | 0 | 0 | 0 | 2 | RTF1_chr15_41412095_41488563 | RTF1 | copy fasta | chr15 | 41412095 | 41488563 |
| t0018 | 0/0 | 2898 | 1 | 1 | 0 | 0 | 0 | 0 | RTF1_chr15_41412095_41488563 | RTF1 | copy fasta | chr15 | 41412095 | 41488563 |
| t0019 | 0/0 | 2898 | 1 | 0 | 0 | 0 | 0 | 1 | RTF1_chr15_41412095_41488563 | RTF1 | copy fasta | chr15 | 41412095 | 41488563 |
| t0020 | 0/0 | 2897 | 1 | 0 | 1 | 0 | 0 | 0 | RTF1_chr15_41412095_41488563 | RTF1 | copy fasta | chr15 | 41412095 | 41488563 |
| t0021 | 0/0 | 2898 | 1 | 1 | 0 | 0 | 0 | 0 | RTF1_chr15_41412095_41488563 | RTF1 | copy fasta | chr15 | 41412095 | 41488563 |
| t0022 | 0/0 | 2898 | 1 | 0 | 0 | 1 | 0 | 0 | RTF1_chr15_41412095_41488563 | RTF1 | copy fasta | chr15 | 41412095 | 41488563 |
| t0023 | 0/0 | 2898 | 1 | 1 | 0 | 0 | 0 | 0 | RTF1_chr15_41412095_41488563 | RTF1 | copy fasta | chr15 | 41412095 | 41488563 |
| t0024 | 0/0 | 2898 | 1 | 0 | 0 | 1 | 0 | 0 | RTF1_chr15_41412095_41488563 | RTF1 | copy fasta | chr15 | 41412095 | 41488563 |
| t0025 | 0/0 | 2898 | 1 | 0 | 0 | 0 | 0 | 1 | RTF1_chr15_41412095_41488563 | RTF1 | copy fasta | chr15 | 41412095 | 41488563 |
| t0026 | 0/0 | 2896 | 1 | 0 | 0 | 0 | 0 | 1 | RTF1_chr15_41412095_41488563 | RTF1 | copy fasta | chr15 | 41412095 | 41488563 |
| t0027 | 0/0 | 2897 | 1 | 1 | 0 | 0 | 0 | 0 | RTF1_chr15_41412095_41488563 | RTF1 | copy fasta | chr15 | 41412095 | 41488563 |
| t0028 | 0/0 | 2897 | 1 | 0 | 0 | 1 | 0 | 0 | RTF1_chr15_41412095_41488563 | RTF1 | copy fasta | chr15 | 41412095 | 41488563 |
| t0029 | 0/0 | 2897 | 1 | 0 | 0 | 1 | 0 | 0 | RTF1_chr15_41412095_41488563 | RTF1 | copy fasta | chr15 | 41412095 | 41488563 |
| t0030 | 0/0 | 2897 | 1 | 0 | 0 | 1 | 0 | 0 | RTF1_chr15_41412095_41488563 | RTF1 | copy fasta | chr15 | 41412095 | 41488563 |
| ghapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| g0001 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | RTF1_chr15_41412095_41488563 | RTF1 | chr15 | 41412095 | 41488563 |
| g0002 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTF1_chr15_41412095_41488563 | RTF1 | chr15 | 41412095 | 41488563 |
| g0003 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RTF1_chr15_41412095_41488563 | RTF1 | chr15 | 41412095 | 41488563 |
| g0004 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTF1_chr15_41412095_41488563 | RTF1 | chr15 | 41412095 | 41488563 |
| g0005 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTF1_chr15_41412095_41488563 | RTF1 | chr15 | 41412095 | 41488563 |
| g0006 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTF1_chr15_41412095_41488563 | RTF1 | chr15 | 41412095 | 41488563 |
| g0007 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RTF1_chr15_41412095_41488563 | RTF1 | chr15 | 41412095 | 41488563 |
| g0008 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RTF1_chr15_41412095_41488563 | RTF1 | chr15 | 41412095 | 41488563 |
| g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTF1_chr15_41412095_41488563 | RTF1 | chr15 | 41412095 | 41488563 |
| g0010 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RTF1_chr15_41412095_41488563 | RTF1 | chr15 | 41412095 | 41488563 |
| g0011 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RTF1_chr15_41412095_41488563 | RTF1 | chr15 | 41412095 | 41488563 |
| g0012 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | RTF1_chr15_41412095_41488563 | RTF1 | chr15 | 41412095 | 41488563 |
| g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTF1_chr15_41412095_41488563 | RTF1 | chr15 | 41412095 | 41488563 |
| g0014 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RTF1_chr15_41412095_41488563 | RTF1 | chr15 | 41412095 | 41488563 |
| g0015 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTF1_chr15_41412095_41488563 | RTF1 | chr15 | 41412095 | 41488563 |
| g0016 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RTF1_chr15_41412095_41488563 | RTF1 | chr15 | 41412095 | 41488563 |
| g0017 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RTF1_chr15_41412095_41488563 | RTF1 | chr15 | 41412095 | 41488563 |
| g0018 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RTF1_chr15_41412095_41488563 | RTF1 | chr15 | 41412095 | 41488563 |
| g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTF1_chr15_41412095_41488563 | RTF1 | chr15 | 41412095 | 41488563 |
| g0020 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RTF1_chr15_41412095_41488563 | RTF1 | chr15 | 41412095 | 41488563 |
| g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTF1_chr15_41412095_41488563 | RTF1 | chr15 | 41412095 | 41488563 |
| g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTF1_chr15_41412095_41488563 | RTF1 | chr15 | 41412095 | 41488563 |
| g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTF1_chr15_41412095_41488563 | RTF1 | chr15 | 41412095 | 41488563 |
| g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTF1_chr15_41412095_41488563 | RTF1 | chr15 | 41412095 | 41488563 |
| g0025 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RTF1_chr15_41412095_41488563 | RTF1 | chr15 | 41412095 | 41488563 |
| g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTF1_chr15_41412095_41488563 | RTF1 | chr15 | 41412095 | 41488563 |
| g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTF1_chr15_41412095_41488563 | RTF1 | chr15 | 41412095 | 41488563 |
| g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTF1_chr15_41412095_41488563 | RTF1 | chr15 | 41412095 | 41488563 |
| g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTF1_chr15_41412095_41488563 | RTF1 | chr15 | 41412095 | 41488563 |
| g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTF1_chr15_41412095_41488563 | RTF1 | chr15 | 41412095 | 41488563 |
| g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTF1_chr15_41412095_41488563 | RTF1 | chr15 | 41412095 | 41488563 |
| g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTF1_chr15_41412095_41488563 | RTF1 | chr15 | 41412095 | 41488563 |
| g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTF1_chr15_41412095_41488563 | RTF1 | chr15 | 41412095 | 41488563 |
| g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTF1_chr15_41412095_41488563 | RTF1 | chr15 | 41412095 | 41488563 |
| g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTF1_chr15_41412095_41488563 | RTF1 | chr15 | 41412095 | 41488563 |
| g0036 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RTF1_chr15_41412095_41488563 | RTF1 | chr15 | 41412095 | 41488563 |
| g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTF1_chr15_41412095_41488563 | RTF1 | chr15 | 41412095 | 41488563 |
| g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTF1_chr15_41412095_41488563 | RTF1 | chr15 | 41412095 | 41488563 |
| g0039 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RTF1_chr15_41412095_41488563 | RTF1 | chr15 | 41412095 | 41488563 |
| g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTF1_chr15_41412095_41488563 | RTF1 | chr15 | 41412095 | 41488563 |
| g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTF1_chr15_41412095_41488563 | RTF1 | chr15 | 41412095 | 41488563 |
| g0042 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RTF1_chr15_41412095_41488563 | RTF1 | chr15 | 41412095 | 41488563 |
| g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTF1_chr15_41412095_41488563 | RTF1 | chr15 | 41412095 | 41488563 |
| g0044 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RTF1_chr15_41412095_41488563 | RTF1 | chr15 | 41412095 | 41488563 |
| g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTF1_chr15_41412095_41488563 | RTF1 | chr15 | 41412095 | 41488563 |
| g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTF1_chr15_41412095_41488563 | RTF1 | chr15 | 41412095 | 41488563 |
| g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTF1_chr15_41412095_41488563 | RTF1 | chr15 | 41412095 | 41488563 |
| g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTF1_chr15_41412095_41488563 | RTF1 | chr15 | 41412095 | 41488563 |
| g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTF1_chr15_41412095_41488563 | RTF1 | chr15 | 41412095 | 41488563 |
| g0050 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RTF1_chr15_41412095_41488563 | RTF1 | chr15 | 41412095 | 41488563 |
| g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTF1_chr15_41412095_41488563 | RTF1 | chr15 | 41412095 | 41488563 |
| g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTF1_chr15_41412095_41488563 | RTF1 | chr15 | 41412095 | 41488563 |
| g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTF1_chr15_41412095_41488563 | RTF1 | chr15 | 41412095 | 41488563 |
| g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTF1_chr15_41412095_41488563 | RTF1 | chr15 | 41412095 | 41488563 |
| g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTF1_chr15_41412095_41488563 | RTF1 | chr15 | 41412095 | 41488563 |
| g0056 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RTF1_chr15_41412095_41488563 | RTF1 | chr15 | 41412095 | 41488563 |
| g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTF1_chr15_41412095_41488563 | RTF1 | chr15 | 41412095 | 41488563 |
| g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTF1_chr15_41412095_41488563 | RTF1 | chr15 | 41412095 | 41488563 |
| g0059 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RTF1_chr15_41412095_41488563 | RTF1 | chr15 | 41412095 | 41488563 |
| g0060 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RTF1_chr15_41412095_41488563 | RTF1 | chr15 | 41412095 | 41488563 |
| g0061 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RTF1_chr15_41412095_41488563 | RTF1 | chr15 | 41412095 | 41488563 |
| g0062 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RTF1_chr15_41412095_41488563 | RTF1 | chr15 | 41412095 | 41488563 |
| g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RTF1_chr15_41412095_41488563 | RTF1 | chr15 | 41412095 | 41488563 |
| g0064 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RTF1_chr15_41412095_41488563 | RTF1 | chr15 | 41412095 | 41488563 |
| g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTF1_chr15_41412095_41488563 | RTF1 | chr15 | 41412095 | 41488563 |
| g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTF1_chr15_41412095_41488563 | RTF1 | chr15 | 41412095 | 41488563 |
| g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTF1_chr15_41412095_41488563 | RTF1 | chr15 | 41412095 | 41488563 |
| g0068 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RTF1_chr15_41412095_41488563 | RTF1 | chr15 | 41412095 | 41488563 |
| g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTF1_chr15_41412095_41488563 | RTF1 | chr15 | 41412095 | 41488563 |
| g0070 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RTF1_chr15_41412095_41488563 | RTF1 | chr15 | 41412095 | 41488563 |
| g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTF1_chr15_41412095_41488563 | RTF1 | chr15 | 41412095 | 41488563 |
| g0072 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RTF1_chr15_41412095_41488563 | RTF1 | chr15 | 41412095 | 41488563 |
| g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RTF1_chr15_41412095_41488563 | RTF1 | chr15 | 41412095 | 41488563 |
| g0074 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RTF1_chr15_41412095_41488563 | RTF1 | chr15 | 41412095 | 41488563 |
| g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTF1_chr15_41412095_41488563 | RTF1 | chr15 | 41412095 | 41488563 |
| g0076 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RTF1_chr15_41412095_41488563 | RTF1 | chr15 | 41412095 | 41488563 |
| g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTF1_chr15_41412095_41488563 | RTF1 | chr15 | 41412095 | 41488563 |
| g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTF1_chr15_41412095_41488563 | RTF1 | chr15 | 41412095 | 41488563 |
| g0079 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RTF1_chr15_41412095_41488563 | RTF1 | chr15 | 41412095 | 41488563 |
| g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTF1_chr15_41412095_41488563 | RTF1 | chr15 | 41412095 | 41488563 |
| g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTF1_chr15_41412095_41488563 | RTF1 | chr15 | 41412095 | 41488563 |
| g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTF1_chr15_41412095_41488563 | RTF1 | chr15 | 41412095 | 41488563 |
| g0083 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RTF1_chr15_41412095_41488563 | RTF1 | chr15 | 41412095 | 41488563 |
| g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTF1_chr15_41412095_41488563 | RTF1 | chr15 | 41412095 | 41488563 |
| g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTF1_chr15_41412095_41488563 | RTF1 | chr15 | 41412095 | 41488563 |
| g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTF1_chr15_41412095_41488563 | RTF1 | chr15 | 41412095 | 41488563 |
| g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTF1_chr15_41412095_41488563 | RTF1 | chr15 | 41412095 | 41488563 |
| g0088 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RTF1_chr15_41412095_41488563 | RTF1 | chr15 | 41412095 | 41488563 |
| g0089 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RTF1_chr15_41412095_41488563 | RTF1 | chr15 | 41412095 | 41488563 |
| g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTF1_chr15_41412095_41488563 | RTF1 | chr15 | 41412095 | 41488563 |
| g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTF1_chr15_41412095_41488563 | RTF1 | chr15 | 41412095 | 41488563 |
| g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTF1_chr15_41412095_41488563 | RTF1 | chr15 | 41412095 | 41488563 |
| g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTF1_chr15_41412095_41488563 | RTF1 | chr15 | 41412095 | 41488563 |
| g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTF1_chr15_41412095_41488563 | RTF1 | chr15 | 41412095 | 41488563 |
| g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTF1_chr15_41412095_41488563 | RTF1 | chr15 | 41412095 | 41488563 |
| g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTF1_chr15_41412095_41488563 | RTF1 | chr15 | 41412095 | 41488563 |
| g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RTF1_chr15_41412095_41488563 | RTF1 | chr15 | 41412095 | 41488563 |
| g0098 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RTF1_chr15_41412095_41488563 | RTF1 | chr15 | 41412095 | 41488563 |
| g0099 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RTF1_chr15_41412095_41488563 | RTF1 | chr15 | 41412095 | 41488563 |
| g0100 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RTF1_chr15_41412095_41488563 | RTF1 | chr15 | 41412095 | 41488563 |
| g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTF1_chr15_41412095_41488563 | RTF1 | chr15 | 41412095 | 41488563 |
| g0102 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | RTF1_chr15_41412095_41488563 | RTF1 | chr15 | 41412095 | 41488563 |
| g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTF1_chr15_41412095_41488563 | RTF1 | chr15 | 41412095 | 41488563 |
| g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTF1_chr15_41412095_41488563 | RTF1 | chr15 | 41412095 | 41488563 |
| g0105 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RTF1_chr15_41412095_41488563 | RTF1 | chr15 | 41412095 | 41488563 |
| g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTF1_chr15_41412095_41488563 | RTF1 | chr15 | 41412095 | 41488563 |
| g0107 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RTF1_chr15_41412095_41488563 | RTF1 | chr15 | 41412095 | 41488563 |
| g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTF1_chr15_41412095_41488563 | RTF1 | chr15 | 41412095 | 41488563 |
| g0109 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RTF1_chr15_41412095_41488563 | RTF1 | chr15 | 41412095 | 41488563 |
| g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTF1_chr15_41412095_41488563 | RTF1 | chr15 | 41412095 | 41488563 |
| g0111 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RTF1_chr15_41412095_41488563 | RTF1 | chr15 | 41412095 | 41488563 |
| g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTF1_chr15_41412095_41488563 | RTF1 | chr15 | 41412095 | 41488563 |
| g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTF1_chr15_41412095_41488563 | RTF1 | chr15 | 41412095 | 41488563 |
| g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTF1_chr15_41412095_41488563 | RTF1 | chr15 | 41412095 | 41488563 |
| g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTF1_chr15_41412095_41488563 | RTF1 | chr15 | 41412095 | 41488563 |
| g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RTF1_chr15_41412095_41488563 | RTF1 | chr15 | 41412095 | 41488563 |
| g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTF1_chr15_41412095_41488563 | RTF1 | chr15 | 41412095 | 41488563 |
| g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTF1_chr15_41412095_41488563 | RTF1 | chr15 | 41412095 | 41488563 |
| g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTF1_chr15_41412095_41488563 | RTF1 | chr15 | 41412095 | 41488563 |
| g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTF1_chr15_41412095_41488563 | RTF1 | chr15 | 41412095 | 41488563 |
| g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTF1_chr15_41412095_41488563 | RTF1 | chr15 | 41412095 | 41488563 |
| g0122 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RTF1_chr15_41412095_41488563 | RTF1 | chr15 | 41412095 | 41488563 |
| g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTF1_chr15_41412095_41488563 | RTF1 | chr15 | 41412095 | 41488563 |
| g0124 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RTF1_chr15_41412095_41488563 | RTF1 | chr15 | 41412095 | 41488563 |
| g0125 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RTF1_chr15_41412095_41488563 | RTF1 | chr15 | 41412095 | 41488563 |
| g0126 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RTF1_chr15_41412095_41488563 | RTF1 | chr15 | 41412095 | 41488563 |
| g0127 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RTF1_chr15_41412095_41488563 | RTF1 | chr15 | 41412095 | 41488563 |
| g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTF1_chr15_41412095_41488563 | RTF1 | chr15 | 41412095 | 41488563 |
| g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTF1_chr15_41412095_41488563 | RTF1 | chr15 | 41412095 | 41488563 |
| g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTF1_chr15_41412095_41488563 | RTF1 | chr15 | 41412095 | 41488563 |
| g0131 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RTF1_chr15_41412095_41488563 | RTF1 | chr15 | 41412095 | 41488563 |
| g0132 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RTF1_chr15_41412095_41488563 | RTF1 | chr15 | 41412095 | 41488563 |
| g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTF1_chr15_41412095_41488563 | RTF1 | chr15 | 41412095 | 41488563 |
| g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTF1_chr15_41412095_41488563 | RTF1 | chr15 | 41412095 | 41488563 |
| g0135 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RTF1_chr15_41412095_41488563 | RTF1 | chr15 | 41412095 | 41488563 |
| g0136 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RTF1_chr15_41412095_41488563 | RTF1 | chr15 | 41412095 | 41488563 |
| g0137 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RTF1_chr15_41412095_41488563 | RTF1 | chr15 | 41412095 | 41488563 |
| g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTF1_chr15_41412095_41488563 | RTF1 | chr15 | 41412095 | 41488563 |
| g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTF1_chr15_41412095_41488563 | RTF1 | chr15 | 41412095 | 41488563 |
| g0140 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RTF1_chr15_41412095_41488563 | RTF1 | chr15 | 41412095 | 41488563 |
| g0141 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RTF1_chr15_41412095_41488563 | RTF1 | chr15 | 41412095 | 41488563 |
| g0142 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RTF1_chr15_41412095_41488563 | RTF1 | chr15 | 41412095 | 41488563 |
| g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTF1_chr15_41412095_41488563 | RTF1 | chr15 | 41412095 | 41488563 |
| g0144 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RTF1_chr15_41412095_41488563 | RTF1 | chr15 | 41412095 | 41488563 |
| g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTF1_chr15_41412095_41488563 | RTF1 | chr15 | 41412095 | 41488563 |
| g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTF1_chr15_41412095_41488563 | RTF1 | chr15 | 41412095 | 41488563 |
| g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTF1_chr15_41412095_41488563 | RTF1 | chr15 | 41412095 | 41488563 |
| g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTF1_chr15_41412095_41488563 | RTF1 | chr15 | 41412095 | 41488563 |
| g0149 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RTF1_chr15_41412095_41488563 | RTF1 | chr15 | 41412095 | 41488563 |
| g0150 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RTF1_chr15_41412095_41488563 | RTF1 | chr15 | 41412095 | 41488563 |
| g0151 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RTF1_chr15_41412095_41488563 | RTF1 | chr15 | 41412095 | 41488563 |
| g0152 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RTF1_chr15_41412095_41488563 | RTF1 | chr15 | 41412095 | 41488563 |
| g0153 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RTF1_chr15_41412095_41488563 | RTF1 | chr15 | 41412095 | 41488563 |
| g0154 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RTF1_chr15_41412095_41488563 | RTF1 | chr15 | 41412095 | 41488563 |
| g0155 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RTF1_chr15_41412095_41488563 | RTF1 | chr15 | 41412095 | 41488563 |
| g0156 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RTF1_chr15_41412095_41488563 | RTF1 | chr15 | 41412095 | 41488563 |
| g0157 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RTF1_chr15_41412095_41488563 | RTF1 | chr15 | 41412095 | 41488563 |
| g0158 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RTF1_chr15_41412095_41488563 | RTF1 | chr15 | 41412095 | 41488563 |
| g0159 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RTF1_chr15_41412095_41488563 | RTF1 | chr15 | 41412095 | 41488563 |
| g0160 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RTF1_chr15_41412095_41488563 | RTF1 | chr15 | 41412095 | 41488563 |
| g0161 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RTF1_chr15_41412095_41488563 | RTF1 | chr15 | 41412095 | 41488563 |
| g0162 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RTF1_chr15_41412095_41488563 | RTF1 | chr15 | 41412095 | 41488563 |
| g0163 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RTF1_chr15_41412095_41488563 | RTF1 | chr15 | 41412095 | 41488563 |
| g0164 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RTF1_chr15_41412095_41488563 | RTF1 | chr15 | 41412095 | 41488563 |
| g0165 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RTF1_chr15_41412095_41488563 | RTF1 | chr15 | 41412095 | 41488563 |
| g0166 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RTF1_chr15_41412095_41488563 | RTF1 | chr15 | 41412095 | 41488563 |
| g0167 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RTF1_chr15_41412095_41488563 | RTF1 | chr15 | 41412095 | 41488563 |
| g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTF1_chr15_41412095_41488563 | RTF1 | chr15 | 41412095 | 41488563 |
| g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTF1_chr15_41412095_41488563 | RTF1 | chr15 | 41412095 | 41488563 |
| g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTF1_chr15_41412095_41488563 | RTF1 | chr15 | 41412095 | 41488563 |
| g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTF1_chr15_41412095_41488563 | RTF1 | chr15 | 41412095 | 41488563 |
| g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTF1_chr15_41412095_41488563 | RTF1 | chr15 | 41412095 | 41488563 |
| g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTF1_chr15_41412095_41488563 | RTF1 | chr15 | 41412095 | 41488563 |
| g0174 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RTF1_chr15_41412095_41488563 | RTF1 | chr15 | 41412095 | 41488563 |
| g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTF1_chr15_41412095_41488563 | RTF1 | chr15 | 41412095 | 41488563 |
| g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTF1_chr15_41412095_41488563 | RTF1 | chr15 | 41412095 | 41488563 |
| g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTF1_chr15_41412095_41488563 | RTF1 | chr15 | 41412095 | 41488563 |
| g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTF1_chr15_41412095_41488563 | RTF1 | chr15 | 41412095 | 41488563 |
| g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTF1_chr15_41412095_41488563 | RTF1 | chr15 | 41412095 | 41488563 |
| g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTF1_chr15_41412095_41488563 | RTF1 | chr15 | 41412095 | 41488563 |
| g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTF1_chr15_41412095_41488563 | RTF1 | chr15 | 41412095 | 41488563 |
| g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTF1_chr15_41412095_41488563 | RTF1 | chr15 | 41412095 | 41488563 |
| g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTF1_chr15_41412095_41488563 | RTF1 | chr15 | 41412095 | 41488563 |
| g0184 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RTF1_chr15_41412095_41488563 | RTF1 | chr15 | 41412095 | 41488563 |
| g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTF1_chr15_41412095_41488563 | RTF1 | chr15 | 41412095 | 41488563 |
| g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTF1_chr15_41412095_41488563 | RTF1 | chr15 | 41412095 | 41488563 |
| g0187 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RTF1_chr15_41412095_41488563 | RTF1 | chr15 | 41412095 | 41488563 |
| g0188 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RTF1_chr15_41412095_41488563 | RTF1 | chr15 | 41412095 | 41488563 |
| g0189 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RTF1_chr15_41412095_41488563 | RTF1 | chr15 | 41412095 | 41488563 |
| g0190 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RTF1_chr15_41412095_41488563 | RTF1 | chr15 | 41412095 | 41488563 |
| g0191 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RTF1_chr15_41412095_41488563 | RTF1 | chr15 | 41412095 | 41488563 |
| g0192 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RTF1_chr15_41412095_41488563 | RTF1 | chr15 | 41412095 | 41488563 |
| g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTF1_chr15_41412095_41488563 | RTF1 | chr15 | 41412095 | 41488563 |
| g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTF1_chr15_41412095_41488563 | RTF1 | chr15 | 41412095 | 41488563 |
| g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTF1_chr15_41412095_41488563 | RTF1 | chr15 | 41412095 | 41488563 |
| g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTF1_chr15_41412095_41488563 | RTF1 | chr15 | 41412095 | 41488563 |
| g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTF1_chr15_41412095_41488563 | RTF1 | chr15 | 41412095 | 41488563 |
| g0198 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RTF1_chr15_41412095_41488563 | RTF1 | chr15 | 41412095 | 41488563 |
| g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTF1_chr15_41412095_41488563 | RTF1 | chr15 | 41412095 | 41488563 |
| g0200 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RTF1_chr15_41412095_41488563 | RTF1 | chr15 | 41412095 | 41488563 |
| g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTF1_chr15_41412095_41488563 | RTF1 | chr15 | 41412095 | 41488563 |
| g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTF1_chr15_41412095_41488563 | RTF1 | chr15 | 41412095 | 41488563 |
| g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTF1_chr15_41412095_41488563 | RTF1 | chr15 | 41412095 | 41488563 |
| g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTF1_chr15_41412095_41488563 | RTF1 | chr15 | 41412095 | 41488563 |
| g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTF1_chr15_41412095_41488563 | RTF1 | chr15 | 41412095 | 41488563 |
| g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTF1_chr15_41412095_41488563 | RTF1 | chr15 | 41412095 | 41488563 |
| g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTF1_chr15_41412095_41488563 | RTF1 | chr15 | 41412095 | 41488563 |
| g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTF1_chr15_41412095_41488563 | RTF1 | chr15 | 41412095 | 41488563 |
| g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTF1_chr15_41412095_41488563 | RTF1 | chr15 | 41412095 | 41488563 |
| g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTF1_chr15_41412095_41488563 | RTF1 | chr15 | 41412095 | 41488563 |
| g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTF1_chr15_41412095_41488563 | RTF1 | chr15 | 41412095 | 41488563 |
| g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTF1_chr15_41412095_41488563 | RTF1 | chr15 | 41412095 | 41488563 |
| g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTF1_chr15_41412095_41488563 | RTF1 | chr15 | 41412095 | 41488563 |
| g0214 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RTF1_chr15_41412095_41488563 | RTF1 | chr15 | 41412095 | 41488563 |
| g0215 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RTF1_chr15_41412095_41488563 | RTF1 | chr15 | 41412095 | 41488563 |
| g0216 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RTF1_chr15_41412095_41488563 | RTF1 | chr15 | 41412095 | 41488563 |
| g0217 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RTF1_chr15_41412095_41488563 | RTF1 | chr15 | 41412095 | 41488563 |
| g0218 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RTF1_chr15_41412095_41488563 | RTF1 | chr15 | 41412095 | 41488563 |
| g0219 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RTF1_chr15_41412095_41488563 | RTF1 | chr15 | 41412095 | 41488563 |
| g0220 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RTF1_chr15_41412095_41488563 | RTF1 | chr15 | 41412095 | 41488563 |
| g0221 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RTF1_chr15_41412095_41488563 | RTF1 | chr15 | 41412095 | 41488563 |
| g0222 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RTF1_chr15_41412095_41488563 | RTF1 | chr15 | 41412095 | 41488563 |
| g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTF1_chr15_41412095_41488563 | RTF1 | chr15 | 41412095 | 41488563 |
| g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTF1_chr15_41412095_41488563 | RTF1 | chr15 | 41412095 | 41488563 |
| g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTF1_chr15_41412095_41488563 | RTF1 | chr15 | 41412095 | 41488563 |
| 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 | 2133 | 219 | 52 | 48 | 72 | 13 | 32 | RTF1_chr15_41412095_41488563 | RTF1 | copy fasta | chr15 | 41412095 | 41488563 |
| a0001c0002 | 0/0 | 2133 | 2 | 2 | 0 | 0 | 0 | 0 | RTF1_chr15_41412095_41488563 | RTF1 | copy fasta | chr15 | 41412095 | 41488563 |
| a0001c0003 | 0/0 | 2133 | 1 | 0 | 0 | 0 | 1 | 0 | RTF1_chr15_41412095_41488563 | RTF1 | copy fasta | chr15 | 41412095 | 41488563 |
| a0001c0004 | 0/0 | 2133 | 1 | 0 | 0 | 1 | 0 | 0 | RTF1_chr15_41412095_41488563 | RTF1 | copy fasta | chr15 | 41412095 | 41488563 |
| a0001c0005 | 0/0 | 2133 | 1 | 0 | 0 | 0 | 0 | 1 | RTF1_chr15_41412095_41488563 | RTF1 | copy fasta | chr15 | 41412095 | 41488563 |
| a0001c0006 | 0/0 | 2133 | 1 | 0 | 0 | 0 | 0 | 1 | RTF1_chr15_41412095_41488563 | RTF1 | copy fasta | chr15 | 41412095 | 41488563 |
| a0002c0007 | 0/0 | 2133 | 1 | 0 | 0 | 1 | 0 | 0 | RTF1_chr15_41412095_41488563 | RTF1 | copy fasta | chr15 | 41412095 | 41488563 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/1 | 5030 | 59 | 15 | 13 | 24 | 1 | 5 | RTF1_chr15_41412095_41488563 | RTF1 | copy fasta | chr15 | 41412095 | 41488563 |
| a0001c0001t0002 | 1/0 | 5030 | 32 | 1 | 6 | 16 | 4 | 4 | RTF1_chr15_41412095_41488563 | RTF1 | copy fasta | chr15 | 41412095 | 41488563 |
| a0001c0001t0003 | 0/0 | 5028 | 26 | 7 | 10 | 1 | 5 | 3 | RTF1_chr15_41412095_41488563 | RTF1 | copy fasta | chr15 | 41412095 | 41488563 |
| a0001c0001t0004 | 0/0 | 5028 | 22 | 1 | 6 | 14 | 0 | 1 | RTF1_chr15_41412095_41488563 | RTF1 | copy fasta | chr15 | 41412095 | 41488563 |
| a0001c0001t0005 | 0/0 | 5027 | 15 | 6 | 4 | 0 | 2 | 3 | RTF1_chr15_41412095_41488563 | RTF1 | copy fasta | chr15 | 41412095 | 41488563 |
| a0001c0001t0006 | 0/0 | 5029 | 11 | 0 | 3 | 4 | 0 | 4 | RTF1_chr15_41412095_41488563 | RTF1 | copy fasta | chr15 | 41412095 | 41488563 |
| a0001c0001t0007 | 0/0 | 5031 | 9 | 2 | 1 | 2 | 0 | 4 | RTF1_chr15_41412095_41488563 | RTF1 | copy fasta | chr15 | 41412095 | 41488563 |
| a0001c0001t0008 | 0/0 | 5031 | 5 | 0 | 0 | 2 | 1 | 2 | RTF1_chr15_41412095_41488563 | RTF1 | copy fasta | chr15 | 41412095 | 41488563 |
| a0001c0001t0009 | 0/0 | 5029 | 7 | 4 | 2 | 1 | 0 | 0 | RTF1_chr15_41412095_41488563 | RTF1 | copy fasta | chr15 | 41412095 | 41488563 |
| a0001c0001t0010 | 0/0 | 5030 | 4 | 4 | 0 | 0 | 0 | 0 | RTF1_chr15_41412095_41488563 | RTF1 | copy fasta | chr15 | 41412095 | 41488563 |
| a0001c0001t0011 | 0/0 | 5028 | 4 | 3 | 1 | 0 | 0 | 0 | RTF1_chr15_41412095_41488563 | RTF1 | copy fasta | chr15 | 41412095 | 41488563 |
| a0001c0001t0012 | 0/0 | 5028 | 3 | 3 | 0 | 0 | 0 | 0 | RTF1_chr15_41412095_41488563 | RTF1 | copy fasta | chr15 | 41412095 | 41488563 |
| a0001c0001t0013 | 0/0 | 5028 | 3 | 0 | 0 | 3 | 0 | 0 | RTF1_chr15_41412095_41488563 | RTF1 | copy fasta | chr15 | 41412095 | 41488563 |
| a0001c0001t0014 | 0/0 | 5028 | 2 | 2 | 0 | 0 | 0 | 0 | RTF1_chr15_41412095_41488563 | RTF1 | copy fasta | chr15 | 41412095 | 41488563 |
| a0001c0001t0016 | 0/0 | 5029 | 2 | 0 | 1 | 0 | 0 | 1 | RTF1_chr15_41412095_41488563 | RTF1 | copy fasta | chr15 | 41412095 | 41488563 |
| a0001c0001t0017 | 0/0 | 5028 | 2 | 0 | 0 | 0 | 0 | 2 | RTF1_chr15_41412095_41488563 | RTF1 | copy fasta | chr15 | 41412095 | 41488563 |
| a0001c0001t0018 | 0/0 | 5030 | 1 | 1 | 0 | 0 | 0 | 0 | RTF1_chr15_41412095_41488563 | RTF1 | copy fasta | chr15 | 41412095 | 41488563 |
| a0001c0001t0019 | 0/0 | 5030 | 1 | 0 | 0 | 0 | 0 | 1 | RTF1_chr15_41412095_41488563 | RTF1 | copy fasta | chr15 | 41412095 | 41488563 |
| a0001c0001t0020 | 0/0 | 5029 | 1 | 0 | 1 | 0 | 0 | 0 | RTF1_chr15_41412095_41488563 | RTF1 | copy fasta | chr15 | 41412095 | 41488563 |
| a0001c0001t0021 | 0/0 | 5030 | 1 | 1 | 0 | 0 | 0 | 0 | RTF1_chr15_41412095_41488563 | RTF1 | copy fasta | chr15 | 41412095 | 41488563 |
| a0001c0001t0022 | 0/0 | 5030 | 1 | 0 | 0 | 1 | 0 | 0 | RTF1_chr15_41412095_41488563 | RTF1 | copy fasta | chr15 | 41412095 | 41488563 |
| a0001c0001t0023 | 0/0 | 5030 | 1 | 1 | 0 | 0 | 0 | 0 | RTF1_chr15_41412095_41488563 | RTF1 | copy fasta | chr15 | 41412095 | 41488563 |
| a0001c0001t0024 | 0/0 | 5030 | 1 | 0 | 0 | 1 | 0 | 0 | RTF1_chr15_41412095_41488563 | RTF1 | copy fasta | chr15 | 41412095 | 41488563 |
| a0001c0001t0025 | 0/0 | 5030 | 1 | 0 | 0 | 0 | 0 | 1 | RTF1_chr15_41412095_41488563 | RTF1 | copy fasta | chr15 | 41412095 | 41488563 |
| a0001c0001t0026 | 0/0 | 5028 | 1 | 0 | 0 | 0 | 0 | 1 | RTF1_chr15_41412095_41488563 | RTF1 | copy fasta | chr15 | 41412095 | 41488563 |
| a0001c0001t0027 | 0/0 | 5029 | 1 | 1 | 0 | 0 | 0 | 0 | RTF1_chr15_41412095_41488563 | RTF1 | copy fasta | chr15 | 41412095 | 41488563 |
| a0001c0001t0028 | 0/0 | 5029 | 1 | 0 | 0 | 1 | 0 | 0 | RTF1_chr15_41412095_41488563 | RTF1 | copy fasta | chr15 | 41412095 | 41488563 |
| a0001c0001t0029 | 0/0 | 5029 | 1 | 0 | 0 | 1 | 0 | 0 | RTF1_chr15_41412095_41488563 | RTF1 | copy fasta | chr15 | 41412095 | 41488563 |
| a0001c0001t0030 | 0/0 | 5029 | 1 | 0 | 0 | 1 | 0 | 0 | RTF1_chr15_41412095_41488563 | RTF1 | copy fasta | chr15 | 41412095 | 41488563 |
| a0001c0002t0015 | 0/0 | 5030 | 2 | 2 | 0 | 0 | 0 | 0 | RTF1_chr15_41412095_41488563 | RTF1 | copy fasta | chr15 | 41412095 | 41488563 |
| a0001c0003t0004 | 0/0 | 5028 | 1 | 0 | 0 | 0 | 1 | 0 | RTF1_chr15_41412095_41488563 | RTF1 | copy fasta | chr15 | 41412095 | 41488563 |
| a0001c0004t0002 | 0/0 | 5030 | 1 | 0 | 0 | 1 | 0 | 0 | RTF1_chr15_41412095_41488563 | RTF1 | copy fasta | chr15 | 41412095 | 41488563 |
| a0001c0005t0007 | 0/0 | 5031 | 1 | 0 | 0 | 0 | 0 | 1 | RTF1_chr15_41412095_41488563 | RTF1 | copy fasta | chr15 | 41412095 | 41488563 |
| a0001c0006t0008 | 0/0 | 5031 | 1 | 0 | 0 | 0 | 0 | 1 | RTF1_chr15_41412095_41488563 | RTF1 | copy fasta | chr15 | 41412095 | 41488563 |
| a0002c0007t0008 | 0/0 | 5031 | 1 | 0 | 0 | 1 | 0 | 0 | RTF1_chr15_41412095_41488563 | RTF1 | copy fasta | chr15 | 41412095 | 41488563 |
| actghapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | RTF1_chr15_41412095_41488563 | RTF1 | chr15 | 41412095 | 41488563 |
| a0001c0001t0001g0005 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTF1_chr15_41412095_41488563 | RTF1 | chr15 | 41412095 | 41488563 |
| a0001c0001t0001g0011 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RTF1_chr15_41412095_41488563 | RTF1 | chr15 | 41412095 | 41488563 |
| a0001c0001t0001g0012 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | RTF1_chr15_41412095_41488563 | RTF1 | chr15 | 41412095 | 41488563 |
| a0001c0001t0001g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTF1_chr15_41412095_41488563 | RTF1 | chr15 | 41412095 | 41488563 |
| a0001c0001t0001g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTF1_chr15_41412095_41488563 | RTF1 | chr15 | 41412095 | 41488563 |
| a0001c0001t0001g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTF1_chr15_41412095_41488563 | RTF1 | chr15 | 41412095 | 41488563 |
| a0001c0001t0001g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTF1_chr15_41412095_41488563 | RTF1 | chr15 | 41412095 | 41488563 |
| a0001c0001t0001g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTF1_chr15_41412095_41488563 | RTF1 | chr15 | 41412095 | 41488563 |
| a0001c0001t0001g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTF1_chr15_41412095_41488563 | RTF1 | chr15 | 41412095 | 41488563 |
| a0001c0001t0001g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTF1_chr15_41412095_41488563 | RTF1 | chr15 | 41412095 | 41488563 |
| a0001c0001t0001g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTF1_chr15_41412095_41488563 | RTF1 | chr15 | 41412095 | 41488563 |
| a0001c0001t0001g0036 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RTF1_chr15_41412095_41488563 | RTF1 | chr15 | 41412095 | 41488563 |
| a0001c0001t0001g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTF1_chr15_41412095_41488563 | RTF1 | chr15 | 41412095 | 41488563 |
| a0001c0001t0001g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTF1_chr15_41412095_41488563 | RTF1 | chr15 | 41412095 | 41488563 |
| a0001c0001t0001g0039 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RTF1_chr15_41412095_41488563 | RTF1 | chr15 | 41412095 | 41488563 |
| a0001c0001t0001g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTF1_chr15_41412095_41488563 | RTF1 | chr15 | 41412095 | 41488563 |
| a0001c0001t0001g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTF1_chr15_41412095_41488563 | RTF1 | chr15 | 41412095 | 41488563 |
| a0001c0001t0001g0042 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RTF1_chr15_41412095_41488563 | RTF1 | chr15 | 41412095 | 41488563 |
| a0001c0001t0001g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTF1_chr15_41412095_41488563 | RTF1 | chr15 | 41412095 | 41488563 |
| a0001c0001t0001g0044 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RTF1_chr15_41412095_41488563 | RTF1 | chr15 | 41412095 | 41488563 |
| a0001c0001t0001g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTF1_chr15_41412095_41488563 | RTF1 | chr15 | 41412095 | 41488563 |
| a0001c0001t0001g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTF1_chr15_41412095_41488563 | RTF1 | chr15 | 41412095 | 41488563 |
| a0001c0001t0001g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTF1_chr15_41412095_41488563 | RTF1 | chr15 | 41412095 | 41488563 |
| a0001c0001t0001g0050 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RTF1_chr15_41412095_41488563 | RTF1 | chr15 | 41412095 | 41488563 |
| a0001c0001t0001g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTF1_chr15_41412095_41488563 | RTF1 | chr15 | 41412095 | 41488563 |
| a0001c0001t0001g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTF1_chr15_41412095_41488563 | RTF1 | chr15 | 41412095 | 41488563 |
| a0001c0001t0001g0056 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RTF1_chr15_41412095_41488563 | RTF1 | chr15 | 41412095 | 41488563 |
| a0001c0001t0001g0059 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RTF1_chr15_41412095_41488563 | RTF1 | chr15 | 41412095 | 41488563 |
| a0001c0001t0001g0060 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RTF1_chr15_41412095_41488563 | RTF1 | chr15 | 41412095 | 41488563 |
| a0001c0001t0001g0062 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RTF1_chr15_41412095_41488563 | RTF1 | chr15 | 41412095 | 41488563 |
| a0001c0001t0001g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RTF1_chr15_41412095_41488563 | RTF1 | chr15 | 41412095 | 41488563 |
| a0001c0001t0001g0064 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RTF1_chr15_41412095_41488563 | RTF1 | chr15 | 41412095 | 41488563 |
| a0001c0001t0001g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTF1_chr15_41412095_41488563 | RTF1 | chr15 | 41412095 | 41488563 |
| a0001c0001t0001g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTF1_chr15_41412095_41488563 | RTF1 | chr15 | 41412095 | 41488563 |
| a0001c0001t0001g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTF1_chr15_41412095_41488563 | RTF1 | chr15 | 41412095 | 41488563 |
| a0001c0001t0001g0068 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RTF1_chr15_41412095_41488563 | RTF1 | chr15 | 41412095 | 41488563 |
| a0001c0001t0001g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTF1_chr15_41412095_41488563 | RTF1 | chr15 | 41412095 | 41488563 |
| a0001c0001t0001g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTF1_chr15_41412095_41488563 | RTF1 | chr15 | 41412095 | 41488563 |
| a0001c0001t0001g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RTF1_chr15_41412095_41488563 | RTF1 | chr15 | 41412095 | 41488563 |
| a0001c0001t0001g0076 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RTF1_chr15_41412095_41488563 | RTF1 | chr15 | 41412095 | 41488563 |
| a0001c0001t0001g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTF1_chr15_41412095_41488563 | RTF1 | chr15 | 41412095 | 41488563 |
| a0001c0001t0001g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTF1_chr15_41412095_41488563 | RTF1 | chr15 | 41412095 | 41488563 |
| a0001c0001t0001g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTF1_chr15_41412095_41488563 | RTF1 | chr15 | 41412095 | 41488563 |
| a0001c0001t0001g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTF1_chr15_41412095_41488563 | RTF1 | chr15 | 41412095 | 41488563 |
| a0001c0001t0001g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTF1_chr15_41412095_41488563 | RTF1 | chr15 | 41412095 | 41488563 |
| a0001c0001t0001g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTF1_chr15_41412095_41488563 | RTF1 | chr15 | 41412095 | 41488563 |
| a0001c0001t0001g0088 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RTF1_chr15_41412095_41488563 | RTF1 | chr15 | 41412095 | 41488563 |
| a0001c0001t0001g0089 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RTF1_chr15_41412095_41488563 | RTF1 | chr15 | 41412095 | 41488563 |
| a0001c0001t0001g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTF1_chr15_41412095_41488563 | RTF1 | chr15 | 41412095 | 41488563 |
| a0001c0001t0001g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTF1_chr15_41412095_41488563 | RTF1 | chr15 | 41412095 | 41488563 |
| a0001c0001t0001g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTF1_chr15_41412095_41488563 | RTF1 | chr15 | 41412095 | 41488563 |
| a0001c0001t0001g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTF1_chr15_41412095_41488563 | RTF1 | chr15 | 41412095 | 41488563 |
| a0001c0001t0001g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTF1_chr15_41412095_41488563 | RTF1 | chr15 | 41412095 | 41488563 |
| a0001c0001t0001g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTF1_chr15_41412095_41488563 | RTF1 | chr15 | 41412095 | 41488563 |
| a0001c0001t0001g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTF1_chr15_41412095_41488563 | RTF1 | chr15 | 41412095 | 41488563 |
| a0001c0001t0001g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTF1_chr15_41412095_41488563 | RTF1 | chr15 | 41412095 | 41488563 |
| a0001c0001t0001g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTF1_chr15_41412095_41488563 | RTF1 | chr15 | 41412095 | 41488563 |
| a0001c0001t0002g0003 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RTF1_chr15_41412095_41488563 | RTF1 | chr15 | 41412095 | 41488563 |
| a0001c0001t0002g0015 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTF1_chr15_41412095_41488563 | RTF1 | chr15 | 41412095 | 41488563 |
| a0001c0001t0002g0016 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RTF1_chr15_41412095_41488563 | RTF1 | chr15 | 41412095 | 41488563 |
| a0001c0001t0002g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTF1_chr15_41412095_41488563 | RTF1 | chr15 | 41412095 | 41488563 |
| a0001c0001t0002g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTF1_chr15_41412095_41488563 | RTF1 | chr15 | 41412095 | 41488563 |
| a0001c0001t0002g0070 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RTF1_chr15_41412095_41488563 | RTF1 | chr15 | 41412095 | 41488563 |
| a0001c0001t0002g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RTF1_chr15_41412095_41488563 | RTF1 | chr15 | 41412095 | 41488563 |
| a0001c0001t0002g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTF1_chr15_41412095_41488563 | RTF1 | chr15 | 41412095 | 41488563 |
| a0001c0001t0002g0102 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | RTF1_chr15_41412095_41488563 | RTF1 | chr15 | 41412095 | 41488563 |
| a0001c0001t0002g0107 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RTF1_chr15_41412095_41488563 | RTF1 | chr15 | 41412095 | 41488563 |
| a0001c0001t0002g0109 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RTF1_chr15_41412095_41488563 | RTF1 | chr15 | 41412095 | 41488563 |
| a0001c0001t0002g0111 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RTF1_chr15_41412095_41488563 | RTF1 | chr15 | 41412095 | 41488563 |
| a0001c0001t0002g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTF1_chr15_41412095_41488563 | RTF1 | chr15 | 41412095 | 41488563 |
| a0001c0001t0002g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTF1_chr15_41412095_41488563 | RTF1 | chr15 | 41412095 | 41488563 |
| a0001c0001t0002g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTF1_chr15_41412095_41488563 | RTF1 | chr15 | 41412095 | 41488563 |
| a0001c0001t0002g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTF1_chr15_41412095_41488563 | RTF1 | chr15 | 41412095 | 41488563 |
| a0001c0001t0002g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTF1_chr15_41412095_41488563 | RTF1 | chr15 | 41412095 | 41488563 |
| a0001c0001t0002g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTF1_chr15_41412095_41488563 | RTF1 | chr15 | 41412095 | 41488563 |
| a0001c0001t0002g0124 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RTF1_chr15_41412095_41488563 | RTF1 | chr15 | 41412095 | 41488563 |
| a0001c0001t0002g0126 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RTF1_chr15_41412095_41488563 | RTF1 | chr15 | 41412095 | 41488563 |
| a0001c0001t0002g0127 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RTF1_chr15_41412095_41488563 | RTF1 | chr15 | 41412095 | 41488563 |
| a0001c0001t0002g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTF1_chr15_41412095_41488563 | RTF1 | chr15 | 41412095 | 41488563 |
| a0001c0001t0002g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTF1_chr15_41412095_41488563 | RTF1 | chr15 | 41412095 | 41488563 |
| a0001c0001t0002g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTF1_chr15_41412095_41488563 | RTF1 | chr15 | 41412095 | 41488563 |
| a0001c0001t0002g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTF1_chr15_41412095_41488563 | RTF1 | chr15 | 41412095 | 41488563 |
| a0001c0001t0002g0135 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RTF1_chr15_41412095_41488563 | RTF1 | chr15 | 41412095 | 41488563 |
| a0001c0001t0002g0136 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RTF1_chr15_41412095_41488563 | RTF1 | chr15 | 41412095 | 41488563 |
| a0001c0001t0002g0137 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RTF1_chr15_41412095_41488563 | RTF1 | chr15 | 41412095 | 41488563 |
| a0001c0001t0002g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTF1_chr15_41412095_41488563 | RTF1 | chr15 | 41412095 | 41488563 |
| a0001c0001t0002g0141 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RTF1_chr15_41412095_41488563 | RTF1 | chr15 | 41412095 | 41488563 |
| a0001c0001t0002g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTF1_chr15_41412095_41488563 | RTF1 | chr15 | 41412095 | 41488563 |
| a0001c0001t0002g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTF1_chr15_41412095_41488563 | RTF1 | chr15 | 41412095 | 41488563 |
| a0001c0001t0003g0002 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTF1_chr15_41412095_41488563 | RTF1 | chr15 | 41412095 | 41488563 |
| a0001c0001t0003g0017 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RTF1_chr15_41412095_41488563 | RTF1 | chr15 | 41412095 | 41488563 |
| a0001c0001t0003g0018 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RTF1_chr15_41412095_41488563 | RTF1 | chr15 | 41412095 | 41488563 |
| a0001c0001t0003g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTF1_chr15_41412095_41488563 | RTF1 | chr15 | 41412095 | 41488563 |
| a0001c0001t0003g0020 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RTF1_chr15_41412095_41488563 | RTF1 | chr15 | 41412095 | 41488563 |
| a0001c0001t0003g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTF1_chr15_41412095_41488563 | RTF1 | chr15 | 41412095 | 41488563 |
| a0001c0001t0003g0149 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RTF1_chr15_41412095_41488563 | RTF1 | chr15 | 41412095 | 41488563 |
| a0001c0001t0003g0151 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RTF1_chr15_41412095_41488563 | RTF1 | chr15 | 41412095 | 41488563 |
| a0001c0001t0003g0153 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RTF1_chr15_41412095_41488563 | RTF1 | chr15 | 41412095 | 41488563 |
| a0001c0001t0003g0156 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RTF1_chr15_41412095_41488563 | RTF1 | chr15 | 41412095 | 41488563 |
| a0001c0001t0003g0157 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RTF1_chr15_41412095_41488563 | RTF1 | chr15 | 41412095 | 41488563 |
| a0001c0001t0003g0158 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RTF1_chr15_41412095_41488563 | RTF1 | chr15 | 41412095 | 41488563 |
| a0001c0001t0003g0159 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RTF1_chr15_41412095_41488563 | RTF1 | chr15 | 41412095 | 41488563 |
| a0001c0001t0003g0160 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RTF1_chr15_41412095_41488563 | RTF1 | chr15 | 41412095 | 41488563 |
| a0001c0001t0003g0161 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RTF1_chr15_41412095_41488563 | RTF1 | chr15 | 41412095 | 41488563 |
| a0001c0001t0003g0162 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RTF1_chr15_41412095_41488563 | RTF1 | chr15 | 41412095 | 41488563 |
| a0001c0001t0003g0163 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RTF1_chr15_41412095_41488563 | RTF1 | chr15 | 41412095 | 41488563 |
| a0001c0001t0003g0164 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RTF1_chr15_41412095_41488563 | RTF1 | chr15 | 41412095 | 41488563 |
| a0001c0001t0003g0166 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RTF1_chr15_41412095_41488563 | RTF1 | chr15 | 41412095 | 41488563 |
| a0001c0001t0003g0167 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RTF1_chr15_41412095_41488563 | RTF1 | chr15 | 41412095 | 41488563 |
| a0001c0001t0003g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTF1_chr15_41412095_41488563 | RTF1 | chr15 | 41412095 | 41488563 |
| a0001c0001t0003g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTF1_chr15_41412095_41488563 | RTF1 | chr15 | 41412095 | 41488563 |
| a0001c0001t0003g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTF1_chr15_41412095_41488563 | RTF1 | chr15 | 41412095 | 41488563 |
| a0001c0001t0003g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTF1_chr15_41412095_41488563 | RTF1 | chr15 | 41412095 | 41488563 |
| a0001c0001t0003g0174 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RTF1_chr15_41412095_41488563 | RTF1 | chr15 | 41412095 | 41488563 |
| a0001c0001t0003g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTF1_chr15_41412095_41488563 | RTF1 | chr15 | 41412095 | 41488563 |
| a0001c0001t0004g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTF1_chr15_41412095_41488563 | RTF1 | chr15 | 41412095 | 41488563 |
| a0001c0001t0004g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTF1_chr15_41412095_41488563 | RTF1 | chr15 | 41412095 | 41488563 |
| a0001c0001t0004g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTF1_chr15_41412095_41488563 | RTF1 | chr15 | 41412095 | 41488563 |
| a0001c0001t0004g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTF1_chr15_41412095_41488563 | RTF1 | chr15 | 41412095 | 41488563 |
| a0001c0001t0004g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTF1_chr15_41412095_41488563 | RTF1 | chr15 | 41412095 | 41488563 |
| a0001c0001t0004g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTF1_chr15_41412095_41488563 | RTF1 | chr15 | 41412095 | 41488563 |
| a0001c0001t0004g0184 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RTF1_chr15_41412095_41488563 | RTF1 | chr15 | 41412095 | 41488563 |
| a0001c0001t0004g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTF1_chr15_41412095_41488563 | RTF1 | chr15 | 41412095 | 41488563 |
| a0001c0001t0004g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTF1_chr15_41412095_41488563 | RTF1 | chr15 | 41412095 | 41488563 |
| a0001c0001t0004g0187 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RTF1_chr15_41412095_41488563 | RTF1 | chr15 | 41412095 | 41488563 |
| a0001c0001t0004g0188 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RTF1_chr15_41412095_41488563 | RTF1 | chr15 | 41412095 | 41488563 |
| a0001c0001t0004g0189 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RTF1_chr15_41412095_41488563 | RTF1 | chr15 | 41412095 | 41488563 |
| a0001c0001t0004g0191 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RTF1_chr15_41412095_41488563 | RTF1 | chr15 | 41412095 | 41488563 |
| a0001c0001t0004g0192 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RTF1_chr15_41412095_41488563 | RTF1 | chr15 | 41412095 | 41488563 |
| a0001c0001t0004g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTF1_chr15_41412095_41488563 | RTF1 | chr15 | 41412095 | 41488563 |
| a0001c0001t0004g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTF1_chr15_41412095_41488563 | RTF1 | chr15 | 41412095 | 41488563 |
| a0001c0001t0004g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTF1_chr15_41412095_41488563 | RTF1 | chr15 | 41412095 | 41488563 |
| a0001c0001t0004g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTF1_chr15_41412095_41488563 | RTF1 | chr15 | 41412095 | 41488563 |
| a0001c0001t0004g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTF1_chr15_41412095_41488563 | RTF1 | chr15 | 41412095 | 41488563 |
| a0001c0001t0004g0198 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RTF1_chr15_41412095_41488563 | RTF1 | chr15 | 41412095 | 41488563 |
| a0001c0001t0004g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTF1_chr15_41412095_41488563 | RTF1 | chr15 | 41412095 | 41488563 |
| a0001c0001t0004g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTF1_chr15_41412095_41488563 | RTF1 | chr15 | 41412095 | 41488563 |
| a0001c0001t0005g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTF1_chr15_41412095_41488563 | RTF1 | chr15 | 41412095 | 41488563 |
| a0001c0001t0005g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTF1_chr15_41412095_41488563 | RTF1 | chr15 | 41412095 | 41488563 |
| a0001c0001t0005g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTF1_chr15_41412095_41488563 | RTF1 | chr15 | 41412095 | 41488563 |
| a0001c0001t0005g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTF1_chr15_41412095_41488563 | RTF1 | chr15 | 41412095 | 41488563 |
| a0001c0001t0005g0214 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RTF1_chr15_41412095_41488563 | RTF1 | chr15 | 41412095 | 41488563 |
| a0001c0001t0005g0215 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RTF1_chr15_41412095_41488563 | RTF1 | chr15 | 41412095 | 41488563 |
| a0001c0001t0005g0216 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RTF1_chr15_41412095_41488563 | RTF1 | chr15 | 41412095 | 41488563 |
| a0001c0001t0005g0217 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RTF1_chr15_41412095_41488563 | RTF1 | chr15 | 41412095 | 41488563 |
| a0001c0001t0005g0218 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RTF1_chr15_41412095_41488563 | RTF1 | chr15 | 41412095 | 41488563 |
| a0001c0001t0005g0219 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RTF1_chr15_41412095_41488563 | RTF1 | chr15 | 41412095 | 41488563 |
| a0001c0001t0005g0220 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RTF1_chr15_41412095_41488563 | RTF1 | chr15 | 41412095 | 41488563 |
| a0001c0001t0005g0221 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RTF1_chr15_41412095_41488563 | RTF1 | chr15 | 41412095 | 41488563 |
| a0001c0001t0005g0222 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RTF1_chr15_41412095_41488563 | RTF1 | chr15 | 41412095 | 41488563 |
| a0001c0001t0005g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTF1_chr15_41412095_41488563 | RTF1 | chr15 | 41412095 | 41488563 |
| a0001c0001t0005g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTF1_chr15_41412095_41488563 | RTF1 | chr15 | 41412095 | 41488563 |
| a0001c0001t0006g0098 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RTF1_chr15_41412095_41488563 | RTF1 | chr15 | 41412095 | 41488563 |
| a0001c0001t0006g0099 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RTF1_chr15_41412095_41488563 | RTF1 | chr15 | 41412095 | 41488563 |
| a0001c0001t0006g0100 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RTF1_chr15_41412095_41488563 | RTF1 | chr15 | 41412095 | 41488563 |
| a0001c0001t0006g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTF1_chr15_41412095_41488563 | RTF1 | chr15 | 41412095 | 41488563 |
| a0001c0001t0006g0105 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RTF1_chr15_41412095_41488563 | RTF1 | chr15 | 41412095 | 41488563 |
| a0001c0001t0006g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTF1_chr15_41412095_41488563 | RTF1 | chr15 | 41412095 | 41488563 |
| a0001c0001t0006g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTF1_chr15_41412095_41488563 | RTF1 | chr15 | 41412095 | 41488563 |
| a0001c0001t0006g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTF1_chr15_41412095_41488563 | RTF1 | chr15 | 41412095 | 41488563 |
| a0001c0001t0006g0131 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RTF1_chr15_41412095_41488563 | RTF1 | chr15 | 41412095 | 41488563 |
| a0001c0001t0006g0132 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RTF1_chr15_41412095_41488563 | RTF1 | chr15 | 41412095 | 41488563 |
| a0001c0001t0006g0140 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RTF1_chr15_41412095_41488563 | RTF1 | chr15 | 41412095 | 41488563 |
| a0001c0001t0007g0010 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RTF1_chr15_41412095_41488563 | RTF1 | chr15 | 41412095 | 41488563 |
| a0001c0001t0007g0025 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RTF1_chr15_41412095_41488563 | RTF1 | chr15 | 41412095 | 41488563 |
| a0001c0001t0007g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTF1_chr15_41412095_41488563 | RTF1 | chr15 | 41412095 | 41488563 |
| a0001c0001t0007g0061 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RTF1_chr15_41412095_41488563 | RTF1 | chr15 | 41412095 | 41488563 |
| a0001c0001t0007g0072 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RTF1_chr15_41412095_41488563 | RTF1 | chr15 | 41412095 | 41488563 |
| a0001c0001t0007g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTF1_chr15_41412095_41488563 | RTF1 | chr15 | 41412095 | 41488563 |
| a0001c0001t0007g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTF1_chr15_41412095_41488563 | RTF1 | chr15 | 41412095 | 41488563 |
| a0001c0001t0007g0125 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RTF1_chr15_41412095_41488563 | RTF1 | chr15 | 41412095 | 41488563 |
| a0001c0001t0007g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTF1_chr15_41412095_41488563 | RTF1 | chr15 | 41412095 | 41488563 |
| a0001c0001t0008g0014 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RTF1_chr15_41412095_41488563 | RTF1 | chr15 | 41412095 | 41488563 |
| a0001c0001t0008g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTF1_chr15_41412095_41488563 | RTF1 | chr15 | 41412095 | 41488563 |
| a0001c0001t0008g0122 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RTF1_chr15_41412095_41488563 | RTF1 | chr15 | 41412095 | 41488563 |
| a0001c0001t0008g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTF1_chr15_41412095_41488563 | RTF1 | chr15 | 41412095 | 41488563 |
| a0001c0001t0008g0142 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RTF1_chr15_41412095_41488563 | RTF1 | chr15 | 41412095 | 41488563 |
| a0001c0001t0009g0004 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTF1_chr15_41412095_41488563 | RTF1 | chr15 | 41412095 | 41488563 |
| a0001c0001t0009g0006 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTF1_chr15_41412095_41488563 | RTF1 | chr15 | 41412095 | 41488563 |
| a0001c0001t0009g0007 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RTF1_chr15_41412095_41488563 | RTF1 | chr15 | 41412095 | 41488563 |
| a0001c0001t0009g0008 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RTF1_chr15_41412095_41488563 | RTF1 | chr15 | 41412095 | 41488563 |
| a0001c0001t0009g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTF1_chr15_41412095_41488563 | RTF1 | chr15 | 41412095 | 41488563 |
| a0001c0001t0009g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTF1_chr15_41412095_41488563 | RTF1 | chr15 | 41412095 | 41488563 |
| a0001c0001t0009g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTF1_chr15_41412095_41488563 | RTF1 | chr15 | 41412095 | 41488563 |
| a0001c0001t0010g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTF1_chr15_41412095_41488563 | RTF1 | chr15 | 41412095 | 41488563 |
| a0001c0001t0010g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTF1_chr15_41412095_41488563 | RTF1 | chr15 | 41412095 | 41488563 |
| a0001c0001t0010g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTF1_chr15_41412095_41488563 | RTF1 | chr15 | 41412095 | 41488563 |
| a0001c0001t0010g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTF1_chr15_41412095_41488563 | RTF1 | chr15 | 41412095 | 41488563 |
| a0001c0001t0011g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTF1_chr15_41412095_41488563 | RTF1 | chr15 | 41412095 | 41488563 |
| a0001c0001t0011g0200 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RTF1_chr15_41412095_41488563 | RTF1 | chr15 | 41412095 | 41488563 |
| a0001c0001t0011g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTF1_chr15_41412095_41488563 | RTF1 | chr15 | 41412095 | 41488563 |
| a0001c0001t0011g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTF1_chr15_41412095_41488563 | RTF1 | chr15 | 41412095 | 41488563 |
| a0001c0001t0012g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTF1_chr15_41412095_41488563 | RTF1 | chr15 | 41412095 | 41488563 |
| a0001c0001t0012g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTF1_chr15_41412095_41488563 | RTF1 | chr15 | 41412095 | 41488563 |
| a0001c0001t0012g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTF1_chr15_41412095_41488563 | RTF1 | chr15 | 41412095 | 41488563 |
| a0001c0001t0013g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTF1_chr15_41412095_41488563 | RTF1 | chr15 | 41412095 | 41488563 |
| a0001c0001t0013g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTF1_chr15_41412095_41488563 | RTF1 | chr15 | 41412095 | 41488563 |
| a0001c0001t0013g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTF1_chr15_41412095_41488563 | RTF1 | chr15 | 41412095 | 41488563 |
| a0001c0001t0014g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTF1_chr15_41412095_41488563 | RTF1 | chr15 | 41412095 | 41488563 |
| a0001c0001t0014g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTF1_chr15_41412095_41488563 | RTF1 | chr15 | 41412095 | 41488563 |
| a0001c0001t0016g0150 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RTF1_chr15_41412095_41488563 | RTF1 | chr15 | 41412095 | 41488563 |
| a0001c0001t0016g0154 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RTF1_chr15_41412095_41488563 | RTF1 | chr15 | 41412095 | 41488563 |
| a0001c0001t0017g0152 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RTF1_chr15_41412095_41488563 | RTF1 | chr15 | 41412095 | 41488563 |
| a0001c0001t0017g0155 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RTF1_chr15_41412095_41488563 | RTF1 | chr15 | 41412095 | 41488563 |
| a0001c0001t0018g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTF1_chr15_41412095_41488563 | RTF1 | chr15 | 41412095 | 41488563 |
| a0001c0001t0019g0079 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RTF1_chr15_41412095_41488563 | RTF1 | chr15 | 41412095 | 41488563 |
| a0001c0001t0020g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RTF1_chr15_41412095_41488563 | RTF1 | chr15 | 41412095 | 41488563 |
| a0001c0001t0021g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTF1_chr15_41412095_41488563 | RTF1 | chr15 | 41412095 | 41488563 |
| a0001c0001t0022g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTF1_chr15_41412095_41488563 | RTF1 | chr15 | 41412095 | 41488563 |
| a0001c0001t0023g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTF1_chr15_41412095_41488563 | RTF1 | chr15 | 41412095 | 41488563 |
| a0001c0001t0024g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTF1_chr15_41412095_41488563 | RTF1 | chr15 | 41412095 | 41488563 |
| a0001c0001t0025g0074 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RTF1_chr15_41412095_41488563 | RTF1 | chr15 | 41412095 | 41488563 |
| a0001c0001t0026g0165 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RTF1_chr15_41412095_41488563 | RTF1 | chr15 | 41412095 | 41488563 |
| a0001c0001t0027g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTF1_chr15_41412095_41488563 | RTF1 | chr15 | 41412095 | 41488563 |
| a0001c0001t0028g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTF1_chr15_41412095_41488563 | RTF1 | chr15 | 41412095 | 41488563 |
| a0001c0001t0029g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTF1_chr15_41412095_41488563 | RTF1 | chr15 | 41412095 | 41488563 |
| a0001c0001t0030g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTF1_chr15_41412095_41488563 | RTF1 | chr15 | 41412095 | 41488563 |
| a0001c0002t0015g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTF1_chr15_41412095_41488563 | RTF1 | chr15 | 41412095 | 41488563 |
| a0001c0002t0015g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RTF1_chr15_41412095_41488563 | RTF1 | chr15 | 41412095 | 41488563 |
| a0001c0003t0004g0190 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RTF1_chr15_41412095_41488563 | RTF1 | chr15 | 41412095 | 41488563 |
| a0001c0004t0002g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTF1_chr15_41412095_41488563 | RTF1 | chr15 | 41412095 | 41488563 |
| a0001c0005t0007g0083 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RTF1_chr15_41412095_41488563 | RTF1 | chr15 | 41412095 | 41488563 |
| a0001c0006t0008g0144 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RTF1_chr15_41412095_41488563 | RTF1 | chr15 | 41412095 | 41488563 |
| a0002c0007t0008g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RTF1_chr15_41412095_41488563 | RTF1 | chr15 | 41412095 | 41488563 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0003 | t0004 | g0190 | EUR | GBR | RTF1_chr15_41412095_41488563 | RTF1 | chr15 | 41412095 | 41488563 |
| HG00099 | hp2 | a0001 | c0001 | t0003 | g0163 | EUR | GBR | RTF1_chr15_41412095_41488563 | RTF1 | chr15 | 41412095 | 41488563 |
| HG00140 | hp1 | a0001 | c0001 | t0003 | g0161 | EUR | GBR | RTF1_chr15_41412095_41488563 | RTF1 | chr15 | 41412095 | 41488563 |
| HG00140 | hp2 | a0001 | c0001 | t0001 | g0036 | EUR | GBR | RTF1_chr15_41412095_41488563 | RTF1 | chr15 | 41412095 | 41488563 |
| HG00280 | hp1 | a0001 | c0001 | t0002 | g0124 | EUR | FIN | RTF1_chr15_41412095_41488563 | RTF1 | chr15 | 41412095 | 41488563 |
| HG00280 | hp2 | a0001 | c0001 | t0008 | g0142 | EUR | FIN | RTF1_chr15_41412095_41488563 | RTF1 | chr15 | 41412095 | 41488563 |
| HG00323 | hp1 | a0001 | c0001 | t0002 | g0141 | EUR | FIN | RTF1_chr15_41412095_41488563 | RTF1 | chr15 | 41412095 | 41488563 |
| HG00323 | hp2 | a0001 | c0001 | t0003 | g0164 | EUR | FIN | RTF1_chr15_41412095_41488563 | RTF1 | chr15 | 41412095 | 41488563 |
| HG00423 | hp1 | a0001 | c0004 | t0002 | g0108 | EAS | CHS | RTF1_chr15_41412095_41488563 | RTF1 | chr15 | 41412095 | 41488563 |
| HG00423 | hp2 | a0001 | c0001 | t0001 | g0065 | EAS | CHS | RTF1_chr15_41412095_41488563 | RTF1 | chr15 | 41412095 | 41488563 |
| HG00544 | hp1 | a0001 | c0001 | t0007 | g0208 | EAS | CHS | RTF1_chr15_41412095_41488563 | RTF1 | chr15 | 41412095 | 41488563 |
| HG00544 | hp2 | a0001 | c0001 | t0006 | g0103 | EAS | CHS | RTF1_chr15_41412095_41488563 | RTF1 | chr15 | 41412095 | 41488563 |
| HG00558 | hp1 | a0001 | c0001 | t0001 | g0053 | EAS | CHS | RTF1_chr15_41412095_41488563 | RTF1 | chr15 | 41412095 | 41488563 |
| HG00558 | hp2 | a0001 | c0001 | t0002 | g0133 | EAS | CHS | RTF1_chr15_41412095_41488563 | RTF1 | chr15 | 41412095 | 41488563 |
| HG00609 | hp1 | a0001 | c0001 | t0004 | g0195 | EAS | CHS | RTF1_chr15_41412095_41488563 | RTF1 | chr15 | 41412095 | 41488563 |
| HG00609 | hp2 | a0001 | c0001 | t0009 | g0084 | EAS | CHS | RTF1_chr15_41412095_41488563 | RTF1 | chr15 | 41412095 | 41488563 |
| HG00639 | hp1 | a0001 | c0001 | t0016 | g0154 | AMR | PUR | RTF1_chr15_41412095_41488563 | RTF1 | chr15 | 41412095 | 41488563 |
| HG00639 | hp2 | a0001 | c0001 | t0006 | g0098 | AMR | PUR | RTF1_chr15_41412095_41488563 | RTF1 | chr15 | 41412095 | 41488563 |
| HG00642 | hp1 | a0001 | c0001 | t0003 | g0149 | AMR | PUR | RTF1_chr15_41412095_41488563 | RTF1 | chr15 | 41412095 | 41488563 |
| HG00642 | hp2 | a0001 | c0001 | t0003 | g0174 | AMR | PUR | RTF1_chr15_41412095_41488563 | RTF1 | chr15 | 41412095 | 41488563 |
| HG00738 | hp1 | a0001 | c0001 | t0006 | g0099 | AMR | PUR | RTF1_chr15_41412095_41488563 | RTF1 | chr15 | 41412095 | 41488563 |
| HG00738 | hp2 | a0001 | c0001 | t0002 | g0109 | AMR | PUR | RTF1_chr15_41412095_41488563 | RTF1 | chr15 | 41412095 | 41488563 |
| HG00741 | hp1 | a0001 | c0001 | t0001 | g0088 | AMR | PUR | RTF1_chr15_41412095_41488563 | RTF1 | chr15 | 41412095 | 41488563 |
| HG00741 | hp2 | a0001 | c0001 | t0003 | g0160 | AMR | PUR | RTF1_chr15_41412095_41488563 | RTF1 | chr15 | 41412095 | 41488563 |
| HG01074 | hp1 | a0001 | c0001 | t0001 | g0050 | AMR | PUR | RTF1_chr15_41412095_41488563 | RTF1 | chr15 | 41412095 | 41488563 |
| HG01074 | hp2 | a0001 | c0001 | t0003 | g0156 | AMR | PUR | RTF1_chr15_41412095_41488563 | RTF1 | chr15 | 41412095 | 41488563 |
| HG01081 | hp1 | a0001 | c0001 | t0003 | g0159 | AMR | PUR | RTF1_chr15_41412095_41488563 | RTF1 | chr15 | 41412095 | 41488563 |
| HG01081 | hp2 | a0001 | c0001 | t0005 | g0217 | AMR | PUR | RTF1_chr15_41412095_41488563 | RTF1 | chr15 | 41412095 | 41488563 |
| HG01106 | hp1 | a0001 | c0001 | t0004 | g0188 | AMR | PUR | RTF1_chr15_41412095_41488563 | RTF1 | chr15 | 41412095 | 41488563 |
| HG01106 | hp2 | a0001 | c0001 | t0005 | g0216 | AMR | PUR | RTF1_chr15_41412095_41488563 | RTF1 | chr15 | 41412095 | 41488563 |
| HG01109 | hp1 | a0001 | c0001 | t0009 | g0008 | AMR | PUR | RTF1_chr15_41412095_41488563 | RTF1 | chr15 | 41412095 | 41488563 |
| HG01109 | hp2 | a0001 | c0001 | t0001 | g0060 | AMR | PUR | RTF1_chr15_41412095_41488563 | RTF1 | chr15 | 41412095 | 41488563 |
| HG01168 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | RTF1_chr15_41412095_41488563 | RTF1 | chr15 | 41412095 | 41488563 |
| HG01168 | hp2 | a0001 | c0001 | t0006 | g0140 | AMR | PUR | RTF1_chr15_41412095_41488563 | RTF1 | chr15 | 41412095 | 41488563 |
| HG01243 | hp1 | a0001 | c0001 | t0009 | g0007 | AMR | PUR | RTF1_chr15_41412095_41488563 | RTF1 | chr15 | 41412095 | 41488563 |
| HG01243 | hp2 | a0001 | c0001 | t0002 | g0126 | AMR | PUR | RTF1_chr15_41412095_41488563 | RTF1 | chr15 | 41412095 | 41488563 |
| HG01257 | hp1 | a0001 | c0001 | t0005 | g0220 | AMR | CLM | RTF1_chr15_41412095_41488563 | RTF1 | chr15 | 41412095 | 41488563 |
| HG01257 | hp2 | a0001 | c0001 | t0001 | g0042 | AMR | CLM | RTF1_chr15_41412095_41488563 | RTF1 | chr15 | 41412095 | 41488563 |
| HG01258 | hp1 | a0001 | c0001 | t0002 | g0107 | AMR | CLM | RTF1_chr15_41412095_41488563 | RTF1 | chr15 | 41412095 | 41488563 |
| HG01258 | hp2 | a0001 | c0001 | t0005 | g0219 | AMR | CLM | RTF1_chr15_41412095_41488563 | RTF1 | chr15 | 41412095 | 41488563 |
| HG01358 | hp1 | a0001 | c0001 | t0003 | g0158 | AMR | CLM | RTF1_chr15_41412095_41488563 | RTF1 | chr15 | 41412095 | 41488563 |
| HG01358 | hp2 | a0001 | c0001 | t0002 | g0111 | AMR | CLM | RTF1_chr15_41412095_41488563 | RTF1 | chr15 | 41412095 | 41488563 |
| HG01361 | hp1 | a0001 | c0001 | t0003 | g0153 | AMR | CLM | RTF1_chr15_41412095_41488563 | RTF1 | chr15 | 41412095 | 41488563 |
| HG01361 | hp2 | a0001 | c0001 | t0001 | g0039 | AMR | CLM | RTF1_chr15_41412095_41488563 | RTF1 | chr15 | 41412095 | 41488563 |
| HG01496 | hp1 | a0001 | c0001 | t0011 | g0200 | AMR | CLM | RTF1_chr15_41412095_41488563 | RTF1 | chr15 | 41412095 | 41488563 |
| HG01496 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | RTF1_chr15_41412095_41488563 | RTF1 | chr15 | 41412095 | 41488563 |
| HG01515 | hp1 | a0001 | c0001 | t0003 | g0018 | EUR | IBS | RTF1_chr15_41412095_41488563 | RTF1 | chr15 | 41412095 | 41488563 |
| HG01515 | hp2 | a0001 | c0001 | t0005 | g0218 | EUR | IBS | RTF1_chr15_41412095_41488563 | RTF1 | chr15 | 41412095 | 41488563 |
| HG01517 | hp1 | a0001 | c0001 | t0005 | g0222 | EUR | IBS | RTF1_chr15_41412095_41488563 | RTF1 | chr15 | 41412095 | 41488563 |
| HG01517 | hp2 | a0001 | c0001 | t0002 | g0003 | EUR | IBS | RTF1_chr15_41412095_41488563 | RTF1 | chr15 | 41412095 | 41488563 |
| HG01884 | hp1 | a0001 | c0001 | t0001 | g0092 | AFR | ACB | RTF1_chr15_41412095_41488563 | RTF1 | chr15 | 41412095 | 41488563 |
| HG01884 | hp2 | a0001 | c0001 | t0001 | g0046 | AFR | ACB | RTF1_chr15_41412095_41488563 | RTF1 | chr15 | 41412095 | 41488563 |
| HG01891 | hp1 | a0001 | c0001 | t0005 | g0213 | AFR | ACB | RTF1_chr15_41412095_41488563 | RTF1 | chr15 | 41412095 | 41488563 |
| HG01891 | hp2 | a0001 | c0001 | t0010 | g0090 | AFR | ACB | RTF1_chr15_41412095_41488563 | RTF1 | chr15 | 41412095 | 41488563 |
| HG01928 | hp1 | a0001 | c0001 | t0001 | g0068 | AMR | PEL | RTF1_chr15_41412095_41488563 | RTF1 | chr15 | 41412095 | 41488563 |
| HG01928 | hp2 | a0001 | c0001 | t0004 | g0184 | AMR | PEL | RTF1_chr15_41412095_41488563 | RTF1 | chr15 | 41412095 | 41488563 |
| HG01975 | hp1 | a0001 | c0001 | t0003 | g0017 | AMR | PEL | RTF1_chr15_41412095_41488563 | RTF1 | chr15 | 41412095 | 41488563 |
| HG01975 | hp2 | a0001 | c0001 | t0004 | g0198 | AMR | PEL | RTF1_chr15_41412095_41488563 | RTF1 | chr15 | 41412095 | 41488563 |
| HG01978 | hp1 | a0001 | c0001 | t0002 | g0097 | AMR | PEL | RTF1_chr15_41412095_41488563 | RTF1 | chr15 | 41412095 | 41488563 |
| HG01978 | hp2 | a0001 | c0001 | t0001 | g0056 | AMR | PEL | RTF1_chr15_41412095_41488563 | RTF1 | chr15 | 41412095 | 41488563 |
| HG01981 | hp1 | a0001 | c0001 | t0004 | g0192 | AMR | PEL | RTF1_chr15_41412095_41488563 | RTF1 | chr15 | 41412095 | 41488563 |
| HG01981 | hp2 | a0001 | c0001 | t0007 | g0072 | AMR | PEL | RTF1_chr15_41412095_41488563 | RTF1 | chr15 | 41412095 | 41488563 |
| HG02004 | hp1 | a0001 | c0001 | t0001 | g0063 | AMR | PEL | RTF1_chr15_41412095_41488563 | RTF1 | chr15 | 41412095 | 41488563 |
| HG02004 | hp2 | a0001 | c0001 | t0004 | g0189 | AMR | PEL | RTF1_chr15_41412095_41488563 | RTF1 | chr15 | 41412095 | 41488563 |
| HG02027 | hp1 | a0001 | c0001 | t0004 | g0186 | EAS | KHV | RTF1_chr15_41412095_41488563 | RTF1 | chr15 | 41412095 | 41488563 |
| HG02027 | hp2 | a0001 | c0001 | t0001 | g0031 | EAS | KHV | RTF1_chr15_41412095_41488563 | RTF1 | chr15 | 41412095 | 41488563 |
| HG02040 | hp1 | a0001 | c0001 | t0001 | g0078 | EAS | KHV | RTF1_chr15_41412095_41488563 | RTF1 | chr15 | 41412095 | 41488563 |
| HG02040 | hp2 | a0001 | c0001 | t0002 | g0128 | EAS | KHV | RTF1_chr15_41412095_41488563 | RTF1 | chr15 | 41412095 | 41488563 |
| HG02055 | hp1 | a0001 | c0001 | t0001 | g0096 | AFR | ACB | RTF1_chr15_41412095_41488563 | RTF1 | chr15 | 41412095 | 41488563 |
| HG02055 | hp2 | a0001 | c0001 | t0012 | g0021 | AFR | ACB | RTF1_chr15_41412095_41488563 | RTF1 | chr15 | 41412095 | 41488563 |
| HG02083 | hp1 | a0001 | c0001 | t0002 | g0121 | EAS | KHV | RTF1_chr15_41412095_41488563 | RTF1 | chr15 | 41412095 | 41488563 |
| HG02083 | hp2 | a0001 | c0001 | t0001 | g0047 | EAS | KHV | RTF1_chr15_41412095_41488563 | RTF1 | chr15 | 41412095 | 41488563 |
| HG02129 | hp1 | a0001 | c0001 | t0001 | g0077 | EAS | KHV | RTF1_chr15_41412095_41488563 | RTF1 | chr15 | 41412095 | 41488563 |
| HG02129 | hp2 | a0001 | c0001 | t0001 | g0041 | EAS | KHV | RTF1_chr15_41412095_41488563 | RTF1 | chr15 | 41412095 | 41488563 |
| HG02145 | hp1 | a0001 | c0001 | t0001 | g0027 | AFR | ACB | RTF1_chr15_41412095_41488563 | RTF1 | chr15 | 41412095 | 41488563 |
| HG02145 | hp2 | a0001 | c0001 | t0009 | g0009 | AFR | ACB | RTF1_chr15_41412095_41488563 | RTF1 | chr15 | 41412095 | 41488563 |
| HG02148 | hp1 | a0001 | c0001 | t0001 | g0044 | AMR | PEL | RTF1_chr15_41412095_41488563 | RTF1 | chr15 | 41412095 | 41488563 |
| HG02148 | hp2 | a0001 | c0001 | t0001 | g0073 | AMR | PEL | RTF1_chr15_41412095_41488563 | RTF1 | chr15 | 41412095 | 41488563 |
| HG02165 | hp1 | a0001 | c0001 | t0001 | g0051 | EAS | CDX | RTF1_chr15_41412095_41488563 | RTF1 | chr15 | 41412095 | 41488563 |
| HG02165 | hp2 | a0001 | c0001 | t0004 | g0197 | EAS | CDX | RTF1_chr15_41412095_41488563 | RTF1 | chr15 | 41412095 | 41488563 |
| HG02273 | hp1 | a0001 | c0001 | t0004 | g0187 | AMR | PEL | RTF1_chr15_41412095_41488563 | RTF1 | chr15 | 41412095 | 41488563 |
| HG02273 | hp2 | a0001 | c0001 | t0001 | g0062 | AMR | PEL | RTF1_chr15_41412095_41488563 | RTF1 | chr15 | 41412095 | 41488563 |
| HG02293 | hp1 | a0001 | c0001 | t0003 | g0151 | AMR | PEL | RTF1_chr15_41412095_41488563 | RTF1 | chr15 | 41412095 | 41488563 |
| HG02293 | hp2 | a0001 | c0001 | t0020 | g0116 | AMR | PEL | RTF1_chr15_41412095_41488563 | RTF1 | chr15 | 41412095 | 41488563 |
| HG02300 | hp1 | a0001 | c0001 | t0003 | g0162 | AMR | PEL | RTF1_chr15_41412095_41488563 | RTF1 | chr15 | 41412095 | 41488563 |
| HG02300 | hp2 | a0001 | c0001 | t0002 | g0127 | AMR | PEL | RTF1_chr15_41412095_41488563 | RTF1 | chr15 | 41412095 | 41488563 |
| HG02451 | hp1 | a0001 | c0001 | t0001 | g0071 | AFR | ACB | RTF1_chr15_41412095_41488563 | RTF1 | chr15 | 41412095 | 41488563 |
| HG02451 | hp2 | a0001 | c0001 | t0011 | g0201 | AFR | ACB | RTF1_chr15_41412095_41488563 | RTF1 | chr15 | 41412095 | 41488563 |
| HG02572 | hp1 | a0001 | c0002 | t0015 | g0057 | AFR | GWD | RTF1_chr15_41412095_41488563 | RTF1 | chr15 | 41412095 | 41488563 |
| HG02572 | hp2 | a0001 | c0001 | t0014 | g0209 | AFR | GWD | RTF1_chr15_41412095_41488563 | RTF1 | chr15 | 41412095 | 41488563 |
| HG02602 | hp1 | a0001 | c0001 | t0025 | g0074 | SAS | PJL | RTF1_chr15_41412095_41488563 | RTF1 | chr15 | 41412095 | 41488563 |
| HG02602 | hp2 | a0001 | c0001 | t0003 | g0166 | SAS | PJL | RTF1_chr15_41412095_41488563 | RTF1 | chr15 | 41412095 | 41488563 |
| HG02615 | hp1 | a0001 | c0001 | t0014 | g0199 | AFR | GWD | RTF1_chr15_41412095_41488563 | RTF1 | chr15 | 41412095 | 41488563 |
| HG02615 | hp2 | a0001 | c0001 | t0007 | g0034 | AFR | GWD | RTF1_chr15_41412095_41488563 | RTF1 | chr15 | 41412095 | 41488563 |
| HG02698 | hp1 | a0001 | c0001 | t0004 | g0191 | SAS | PJL | RTF1_chr15_41412095_41488563 | RTF1 | chr15 | 41412095 | 41488563 |
| HG02698 | hp2 | a0001 | c0001 | t0002 | g0135 | SAS | PJL | RTF1_chr15_41412095_41488563 | RTF1 | chr15 | 41412095 | 41488563 |
| HG02717 | hp1 | a0001 | c0001 | t0018 | g0207 | AFR | GWD | RTF1_chr15_41412095_41488563 | RTF1 | chr15 | 41412095 | 41488563 |
| HG02717 | hp2 | a0001 | c0001 | t0002 | g0143 | AFR | GWD | RTF1_chr15_41412095_41488563 | RTF1 | chr15 | 41412095 | 41488563 |
| HG02809 | hp1 | a0001 | c0001 | t0001 | g0029 | AFR | GWD | RTF1_chr15_41412095_41488563 | RTF1 | chr15 | 41412095 | 41488563 |
| HG02809 | hp2 | a0001 | c0001 | t0003 | g0169 | AFR | GWD | RTF1_chr15_41412095_41488563 | RTF1 | chr15 | 41412095 | 41488563 |
| HG02896 | hp1 | a0001 | c0001 | t0010 | g0052 | AFR | GWD | RTF1_chr15_41412095_41488563 | RTF1 | chr15 | 41412095 | 41488563 |
| HG02896 | hp2 | a0001 | c0001 | t0001 | g0094 | AFR | GWD | RTF1_chr15_41412095_41488563 | RTF1 | chr15 | 41412095 | 41488563 |
| HG02922 | hp1 | a0001 | c0001 | t0009 | g0006 | AFR | ESN | RTF1_chr15_41412095_41488563 | RTF1 | chr15 | 41412095 | 41488563 |
| HG02922 | hp2 | a0001 | c0001 | t0003 | g0002 | AFR | ESN | RTF1_chr15_41412095_41488563 | RTF1 | chr15 | 41412095 | 41488563 |
| HG02965 | hp1 | a0001 | c0001 | t0001 | g0033 | AFR | ESN | RTF1_chr15_41412095_41488563 | RTF1 | chr15 | 41412095 | 41488563 |
| HG02965 | hp2 | a0001 | c0001 | t0003 | g0172 | AFR | ESN | RTF1_chr15_41412095_41488563 | RTF1 | chr15 | 41412095 | 41488563 |
| HG02976 | hp1 | a0001 | c0001 | t0005 | g0224 | AFR | ESN | RTF1_chr15_41412095_41488563 | RTF1 | chr15 | 41412095 | 41488563 |
| HG02976 | hp2 | a0001 | c0001 | t0021 | g0148 | AFR | ESN | RTF1_chr15_41412095_41488563 | RTF1 | chr15 | 41412095 | 41488563 |
| HG03017 | hp1 | a0001 | c0001 | t0007 | g0025 | SAS | PJL | RTF1_chr15_41412095_41488563 | RTF1 | chr15 | 41412095 | 41488563 |
| HG03017 | hp2 | a0001 | c0001 | t0008 | g0122 | SAS | PJL | RTF1_chr15_41412095_41488563 | RTF1 | chr15 | 41412095 | 41488563 |
| HG03041 | hp1 | a0001 | c0001 | t0005 | g0211 | AFR | GWD | RTF1_chr15_41412095_41488563 | RTF1 | chr15 | 41412095 | 41488563 |
| HG03041 | hp2 | a0001 | c0001 | t0001 | g0095 | AFR | GWD | RTF1_chr15_41412095_41488563 | RTF1 | chr15 | 41412095 | 41488563 |
| HG03098 | hp1 | a0001 | c0001 | t0001 | g0013 | AFR | MSL | RTF1_chr15_41412095_41488563 | RTF1 | chr15 | 41412095 | 41488563 |
| HG03098 | hp2 | a0001 | c0001 | t0003 | g0175 | AFR | MSL | RTF1_chr15_41412095_41488563 | RTF1 | chr15 | 41412095 | 41488563 |
| HG03130 | hp1 | a0001 | c0001 | t0012 | g0168 | AFR | ESN | RTF1_chr15_41412095_41488563 | RTF1 | chr15 | 41412095 | 41488563 |
| HG03130 | hp2 | a0001 | c0001 | t0010 | g0054 | AFR | ESN | RTF1_chr15_41412095_41488563 | RTF1 | chr15 | 41412095 | 41488563 |
| HG03139 | hp1 | a0001 | c0001 | t0023 | g0146 | AFR | ESN | RTF1_chr15_41412095_41488563 | RTF1 | chr15 | 41412095 | 41488563 |
| HG03139 | hp2 | a0001 | c0001 | t0005 | g0212 | AFR | ESN | RTF1_chr15_41412095_41488563 | RTF1 | chr15 | 41412095 | 41488563 |
| HG03195 | hp1 | a0001 | c0001 | t0003 | g0173 | AFR | ESN | RTF1_chr15_41412095_41488563 | RTF1 | chr15 | 41412095 | 41488563 |
| HG03195 | hp2 | a0001 | c0001 | t0011 | g0202 | AFR | ESN | RTF1_chr15_41412095_41488563 | RTF1 | chr15 | 41412095 | 41488563 |
| HG03453 | hp1 | a0001 | c0001 | t0009 | g0028 | AFR | MSL | RTF1_chr15_41412095_41488563 | RTF1 | chr15 | 41412095 | 41488563 |
| HG03453 | hp2 | a0001 | c0001 | t0007 | g0075 | AFR | MSL | RTF1_chr15_41412095_41488563 | RTF1 | chr15 | 41412095 | 41488563 |
| HG03486 | hp1 | a0001 | c0001 | t0027 | g0147 | AFR | MSL | RTF1_chr15_41412095_41488563 | RTF1 | chr15 | 41412095 | 41488563 |
| HG03486 | hp2 | a0001 | c0001 | t0012 | g0171 | AFR | MSL | RTF1_chr15_41412095_41488563 | RTF1 | chr15 | 41412095 | 41488563 |
| HG03491 | hp1 | a0001 | c0001 | t0017 | g0152 | SAS | PJL | RTF1_chr15_41412095_41488563 | RTF1 | chr15 | 41412095 | 41488563 |
| HG03491 | hp2 | a0001 | c0006 | t0008 | g0144 | SAS | PJL | RTF1_chr15_41412095_41488563 | RTF1 | chr15 | 41412095 | 41488563 |
| HG03492 | hp1 | a0001 | c0001 | t0001 | g0076 | SAS | PJL | RTF1_chr15_41412095_41488563 | RTF1 | chr15 | 41412095 | 41488563 |
| HG03492 | hp2 | a0001 | c0001 | t0017 | g0155 | SAS | PJL | RTF1_chr15_41412095_41488563 | RTF1 | chr15 | 41412095 | 41488563 |
| HG03540 | hp1 | a0001 | c0001 | t0011 | g0023 | AFR | GWD | RTF1_chr15_41412095_41488563 | RTF1 | chr15 | 41412095 | 41488563 |
| HG03540 | hp2 | a0001 | c0001 | t0001 | g0067 | AFR | GWD | RTF1_chr15_41412095_41488563 | RTF1 | chr15 | 41412095 | 41488563 |
| HG03654 | hp1 | a0001 | c0001 | t0006 | g0100 | SAS | PJL | RTF1_chr15_41412095_41488563 | RTF1 | chr15 | 41412095 | 41488563 |
| HG03654 | hp2 | a0001 | c0001 | t0001 | g0089 | SAS | PJL | RTF1_chr15_41412095_41488563 | RTF1 | chr15 | 41412095 | 41488563 |
| HG03669 | hp1 | a0001 | c0001 | t0008 | g0014 | SAS | PJL | RTF1_chr15_41412095_41488563 | RTF1 | chr15 | 41412095 | 41488563 |
| HG03669 | hp2 | a0001 | c0001 | t0001 | g0059 | SAS | PJL | RTF1_chr15_41412095_41488563 | RTF1 | chr15 | 41412095 | 41488563 |
| HG03704 | hp1 | a0001 | c0001 | t0002 | g0070 | SAS | PJL | RTF1_chr15_41412095_41488563 | RTF1 | chr15 | 41412095 | 41488563 |
| HG03704 | hp2 | a0001 | c0001 | t0007 | g0125 | SAS | PJL | RTF1_chr15_41412095_41488563 | RTF1 | chr15 | 41412095 | 41488563 |
| HG03834 | hp1 | a0001 | c0001 | t0002 | g0136 | SAS | BEB | RTF1_chr15_41412095_41488563 | RTF1 | chr15 | 41412095 | 41488563 |
| HG03834 | hp2 | a0001 | c0001 | t0026 | g0165 | SAS | BEB | RTF1_chr15_41412095_41488563 | RTF1 | chr15 | 41412095 | 41488563 |
| HG03927 | hp1 | a0001 | c0001 | t0007 | g0061 | SAS | BEB | RTF1_chr15_41412095_41488563 | RTF1 | chr15 | 41412095 | 41488563 |
| HG03927 | hp2 | a0001 | c0001 | t0006 | g0132 | SAS | BEB | RTF1_chr15_41412095_41488563 | RTF1 | chr15 | 41412095 | 41488563 |
| HG03942 | hp1 | a0001 | c0001 | t0007 | g0010 | SAS | BEB | RTF1_chr15_41412095_41488563 | RTF1 | chr15 | 41412095 | 41488563 |
| HG03942 | hp2 | a0001 | c0001 | t0003 | g0020 | SAS | BEB | RTF1_chr15_41412095_41488563 | RTF1 | chr15 | 41412095 | 41488563 |
| HG04115 | hp1 | a0001 | c0001 | t0001 | g0011 | SAS | STU | RTF1_chr15_41412095_41488563 | RTF1 | chr15 | 41412095 | 41488563 |
| HG04115 | hp2 | a0001 | c0001 | t0002 | g0016 | SAS | STU | RTF1_chr15_41412095_41488563 | RTF1 | chr15 | 41412095 | 41488563 |
| HG04184 | hp1 | a0001 | c0001 | t0016 | g0150 | SAS | BEB | RTF1_chr15_41412095_41488563 | RTF1 | chr15 | 41412095 | 41488563 |
| HG04184 | hp2 | a0001 | c0001 | t0019 | g0079 | SAS | BEB | RTF1_chr15_41412095_41488563 | RTF1 | chr15 | 41412095 | 41488563 |
| HG04199 | hp1 | a0001 | c0001 | t0005 | g0214 | SAS | STU | RTF1_chr15_41412095_41488563 | RTF1 | chr15 | 41412095 | 41488563 |
| HG04199 | hp2 | a0001 | c0001 | t0006 | g0105 | SAS | STU | RTF1_chr15_41412095_41488563 | RTF1 | chr15 | 41412095 | 41488563 |
| HG04204 | hp1 | a0001 | c0005 | t0007 | g0083 | SAS | STU | RTF1_chr15_41412095_41488563 | RTF1 | chr15 | 41412095 | 41488563 |
| HG04204 | hp2 | a0001 | c0001 | t0005 | g0221 | SAS | STU | RTF1_chr15_41412095_41488563 | RTF1 | chr15 | 41412095 | 41488563 |
| HG04228 | hp1 | a0001 | c0001 | t0003 | g0167 | SAS | STU | RTF1_chr15_41412095_41488563 | RTF1 | chr15 | 41412095 | 41488563 |
| HG04228 | hp2 | a0001 | c0001 | t0006 | g0131 | SAS | STU | RTF1_chr15_41412095_41488563 | RTF1 | chr15 | 41412095 | 41488563 |
| NA18906 | hp1 | a0001 | c0001 | t0001 | g0030 | AFR | YRI | RTF1_chr15_41412095_41488563 | RTF1 | chr15 | 41412095 | 41488563 |
| NA18906 | hp2 | a0001 | c0001 | t0009 | g0004 | AFR | YRI | RTF1_chr15_41412095_41488563 | RTF1 | chr15 | 41412095 | 41488563 |
| NA18943 | hp1 | a0001 | c0001 | t0024 | g0045 | EAS | JPT | RTF1_chr15_41412095_41488563 | RTF1 | chr15 | 41412095 | 41488563 |
| NA18943 | hp2 | a0001 | c0001 | t0004 | g0193 | EAS | JPT | RTF1_chr15_41412095_41488563 | RTF1 | chr15 | 41412095 | 41488563 |
| NA18944 | hp1 | a0001 | c0001 | t0004 | g0194 | EAS | JPT | RTF1_chr15_41412095_41488563 | RTF1 | chr15 | 41412095 | 41488563 |
| NA18944 | hp2 | a0001 | c0001 | t0001 | g0086 | EAS | JPT | RTF1_chr15_41412095_41488563 | RTF1 | chr15 | 41412095 | 41488563 |
| NA18946 | hp1 | a0001 | c0001 | t0001 | g0026 | EAS | JPT | RTF1_chr15_41412095_41488563 | RTF1 | chr15 | 41412095 | 41488563 |
| NA18946 | hp2 | a0001 | c0001 | t0002 | g0123 | EAS | JPT | RTF1_chr15_41412095_41488563 | RTF1 | chr15 | 41412095 | 41488563 |
| NA18949 | hp1 | a0001 | c0001 | t0004 | g0179 | EAS | JPT | RTF1_chr15_41412095_41488563 | RTF1 | chr15 | 41412095 | 41488563 |
| NA18949 | hp2 | a0001 | c0001 | t0002 | g0114 | EAS | JPT | RTF1_chr15_41412095_41488563 | RTF1 | chr15 | 41412095 | 41488563 |
| NA18953 | hp1 | a0001 | c0001 | t0001 | g0138 | EAS | JPT | RTF1_chr15_41412095_41488563 | RTF1 | chr15 | 41412095 | 41488563 |
| NA18953 | hp2 | a0001 | c0001 | t0002 | g0139 | EAS | JPT | RTF1_chr15_41412095_41488563 | RTF1 | chr15 | 41412095 | 41488563 |
| NA18960 | hp1 | a0001 | c0001 | t0001 | g0043 | EAS | JPT | RTF1_chr15_41412095_41488563 | RTF1 | chr15 | 41412095 | 41488563 |
| NA18960 | hp2 | a0001 | c0001 | t0002 | g0119 | EAS | JPT | RTF1_chr15_41412095_41488563 | RTF1 | chr15 | 41412095 | 41488563 |
| NA18961 | hp1 | a0001 | c0001 | t0006 | g0118 | EAS | JPT | RTF1_chr15_41412095_41488563 | RTF1 | chr15 | 41412095 | 41488563 |
| NA18961 | hp2 | a0001 | c0001 | t0004 | g0178 | EAS | JPT | RTF1_chr15_41412095_41488563 | RTF1 | chr15 | 41412095 | 41488563 |
| NA18962 | hp1 | a0001 | c0001 | t0004 | g0185 | EAS | JPT | RTF1_chr15_41412095_41488563 | RTF1 | chr15 | 41412095 | 41488563 |
| NA18962 | hp2 | a0001 | c0001 | t0008 | g0129 | EAS | JPT | RTF1_chr15_41412095_41488563 | RTF1 | chr15 | 41412095 | 41488563 |
| NA18964 | hp1 | a0001 | c0001 | t0006 | g0120 | EAS | JPT | RTF1_chr15_41412095_41488563 | RTF1 | chr15 | 41412095 | 41488563 |
| NA18964 | hp2 | a0001 | c0001 | t0004 | g0181 | EAS | JPT | RTF1_chr15_41412095_41488563 | RTF1 | chr15 | 41412095 | 41488563 |
| NA18968 | hp1 | a0001 | c0001 | t0002 | g0101 | EAS | JPT | RTF1_chr15_41412095_41488563 | RTF1 | chr15 | 41412095 | 41488563 |
| NA18968 | hp2 | a0001 | c0001 | t0013 | g0205 | EAS | JPT | RTF1_chr15_41412095_41488563 | RTF1 | chr15 | 41412095 | 41488563 |
| NA18971 | hp1 | a0002 | c0007 | t0008 | g0110 | EAS | JPT | RTF1_chr15_41412095_41488563 | RTF1 | chr15 | 41412095 | 41488563 |
| NA18971 | hp2 | a0001 | c0001 | t0013 | g0204 | EAS | JPT | RTF1_chr15_41412095_41488563 | RTF1 | chr15 | 41412095 | 41488563 |
| NA18975 | hp1 | a0001 | c0001 | t0028 | g0176 | EAS | JPT | RTF1_chr15_41412095_41488563 | RTF1 | chr15 | 41412095 | 41488563 |
| NA18975 | hp2 | a0001 | c0001 | t0002 | g0113 | EAS | JPT | RTF1_chr15_41412095_41488563 | RTF1 | chr15 | 41412095 | 41488563 |
| NA18977 | hp1 | a0001 | c0001 | t0004 | g0225 | EAS | JPT | RTF1_chr15_41412095_41488563 | RTF1 | chr15 | 41412095 | 41488563 |
| NA18977 | hp2 | a0001 | c0001 | t0001 | g0066 | EAS | JPT | RTF1_chr15_41412095_41488563 | RTF1 | chr15 | 41412095 | 41488563 |
| NA18980 | hp1 | a0001 | c0001 | t0006 | g0112 | EAS | JPT | RTF1_chr15_41412095_41488563 | RTF1 | chr15 | 41412095 | 41488563 |
| NA18980 | hp2 | a0001 | c0001 | t0001 | g0035 | EAS | JPT | RTF1_chr15_41412095_41488563 | RTF1 | chr15 | 41412095 | 41488563 |
| NA18983 | hp1 | a0001 | c0001 | t0001 | g0080 | EAS | JPT | RTF1_chr15_41412095_41488563 | RTF1 | chr15 | 41412095 | 41488563 |
| NA18983 | hp2 | a0001 | c0001 | t0004 | g0206 | EAS | JPT | RTF1_chr15_41412095_41488563 | RTF1 | chr15 | 41412095 | 41488563 |
| NA18986 | hp1 | a0001 | c0001 | t0001 | g0038 | EAS | JPT | RTF1_chr15_41412095_41488563 | RTF1 | chr15 | 41412095 | 41488563 |
| NA18986 | hp2 | a0001 | c0001 | t0004 | g0183 | EAS | JPT | RTF1_chr15_41412095_41488563 | RTF1 | chr15 | 41412095 | 41488563 |
| NA18999 | hp1 | a0001 | c0001 | t0001 | g0040 | EAS | JPT | RTF1_chr15_41412095_41488563 | RTF1 | chr15 | 41412095 | 41488563 |
| NA18999 | hp2 | a0001 | c0001 | t0002 | g0145 | EAS | JPT | RTF1_chr15_41412095_41488563 | RTF1 | chr15 | 41412095 | 41488563 |
| NA19009 | hp1 | a0001 | c0001 | t0001 | g0037 | EAS | JPT | RTF1_chr15_41412095_41488563 | RTF1 | chr15 | 41412095 | 41488563 |
| NA19009 | hp2 | a0001 | c0001 | t0002 | g0115 | EAS | JPT | RTF1_chr15_41412095_41488563 | RTF1 | chr15 | 41412095 | 41488563 |
| NA19010 | hp1 | a0001 | c0001 | t0001 | g0048 | EAS | JPT | RTF1_chr15_41412095_41488563 | RTF1 | chr15 | 41412095 | 41488563 |
| NA19010 | hp2 | a0001 | c0001 | t0002 | g0130 | EAS | JPT | RTF1_chr15_41412095_41488563 | RTF1 | chr15 | 41412095 | 41488563 |
| NA19011 | hp1 | a0001 | c0001 | t0008 | g0104 | EAS | JPT | RTF1_chr15_41412095_41488563 | RTF1 | chr15 | 41412095 | 41488563 |
| NA19011 | hp2 | a0001 | c0001 | t0004 | g0196 | EAS | JPT | RTF1_chr15_41412095_41488563 | RTF1 | chr15 | 41412095 | 41488563 |
| NA19043 | hp1 | a0001 | c0001 | t0001 | g0093 | AFR | LWK | RTF1_chr15_41412095_41488563 | RTF1 | chr15 | 41412095 | 41488563 |
| NA19043 | hp2 | a0001 | c0001 | t0005 | g0210 | AFR | LWK | RTF1_chr15_41412095_41488563 | RTF1 | chr15 | 41412095 | 41488563 |
| NA19060 | hp1 | a0001 | c0001 | t0002 | g0015 | EAS | JPT | RTF1_chr15_41412095_41488563 | RTF1 | chr15 | 41412095 | 41488563 |
| NA19060 | hp2 | a0001 | c0001 | t0003 | g0019 | EAS | JPT | RTF1_chr15_41412095_41488563 | RTF1 | chr15 | 41412095 | 41488563 |
| NA19063 | hp1 | a0001 | c0001 | t0004 | g0177 | EAS | JPT | RTF1_chr15_41412095_41488563 | RTF1 | chr15 | 41412095 | 41488563 |
| NA19063 | hp2 | a0001 | c0001 | t0001 | g0085 | EAS | JPT | RTF1_chr15_41412095_41488563 | RTF1 | chr15 | 41412095 | 41488563 |
| NA19074 | hp1 | a0001 | c0001 | t0001 | g0117 | EAS | JPT | RTF1_chr15_41412095_41488563 | RTF1 | chr15 | 41412095 | 41488563 |
| NA19074 | hp2 | a0001 | c0001 | t0002 | g0058 | EAS | JPT | RTF1_chr15_41412095_41488563 | RTF1 | chr15 | 41412095 | 41488563 |
| NA19083 | hp1 | a0001 | c0001 | t0029 | g0203 | EAS | JPT | RTF1_chr15_41412095_41488563 | RTF1 | chr15 | 41412095 | 41488563 |
| NA19083 | hp2 | a0001 | c0001 | t0007 | g0087 | EAS | JPT | RTF1_chr15_41412095_41488563 | RTF1 | chr15 | 41412095 | 41488563 |
| NA19085 | hp1 | a0001 | c0001 | t0030 | g0180 | EAS | JPT | RTF1_chr15_41412095_41488563 | RTF1 | chr15 | 41412095 | 41488563 |
| NA19085 | hp2 | a0001 | c0001 | t0022 | g0081 | EAS | JPT | RTF1_chr15_41412095_41488563 | RTF1 | chr15 | 41412095 | 41488563 |
| NA19089 | hp1 | a0001 | c0001 | t0001 | g0106 | EAS | JPT | RTF1_chr15_41412095_41488563 | RTF1 | chr15 | 41412095 | 41488563 |
| NA19089 | hp2 | a0001 | c0001 | t0002 | g0049 | EAS | JPT | RTF1_chr15_41412095_41488563 | RTF1 | chr15 | 41412095 | 41488563 |
| NA19091 | hp1 | a0001 | c0001 | t0001 | g0082 | EAS | JPT | RTF1_chr15_41412095_41488563 | RTF1 | chr15 | 41412095 | 41488563 |
| NA19091 | hp2 | a0001 | c0001 | t0002 | g0134 | EAS | JPT | RTF1_chr15_41412095_41488563 | RTF1 | chr15 | 41412095 | 41488563 |
| NA20129 | hp1 | a0001 | c0001 | t0001 | g0005 | AFR | ASW | RTF1_chr15_41412095_41488563 | RTF1 | chr15 | 41412095 | 41488563 |
| NA20129 | hp2 | a0001 | c0002 | t0015 | g0032 | AFR | ASW | RTF1_chr15_41412095_41488563 | RTF1 | chr15 | 41412095 | 41488563 |
| NA20805 | hp1 | a0001 | c0001 | t0002 | g0137 | EUR | TSI | RTF1_chr15_41412095_41488563 | RTF1 | chr15 | 41412095 | 41488563 |
| NA20805 | hp2 | a0001 | c0001 | t0003 | g0157 | EUR | TSI | RTF1_chr15_41412095_41488563 | RTF1 | chr15 | 41412095 | 41488563 |
| NA20905 | hp1 | a0001 | c0001 | t0001 | g0064 | SAS | GIH | RTF1_chr15_41412095_41488563 | RTF1 | chr15 | 41412095 | 41488563 |
| NA20905 | hp2 | a0001 | c0001 | t0005 | g0215 | SAS | GIH | RTF1_chr15_41412095_41488563 | RTF1 | chr15 | 41412095 | 41488563 |
| HG02486 | hp1 | a0001 | c0001 | t0003 | g0170 | AFR | ACB | RTF1_chr15_41412095_41488563 | RTF1 | chr15 | 41412095 | 41488563 |
| HG02486 | hp2 | a0001 | c0001 | t0004 | g0182 | AFR | ACB | RTF1_chr15_41412095_41488563 | RTF1 | chr15 | 41412095 | 41488563 |
| NA18955 | hp1 | a0001 | c0001 | t0001 | g0069 | EAS | JPT | RTF1_chr15_41412095_41488563 | RTF1 | chr15 | 41412095 | 41488563 |
| NA18955 | hp2 | a0001 | c0001 | t0013 | g0024 | EAS | JPT | RTF1_chr15_41412095_41488563 | RTF1 | chr15 | 41412095 | 41488563 |
| NA20300 | hp1 | a0001 | c0001 | t0010 | g0055 | AFR | USA | RTF1_chr15_41412095_41488563 | RTF1 | chr15 | 41412095 | 41488563 |
| NA20300 | hp2 | a0001 | c0001 | t0003 | g0022 | AFR | USA | RTF1_chr15_41412095_41488563 | RTF1 | chr15 | 41412095 | 41488563 |
| NA21309 | hp1 | a0001 | c0001 | t0001 | g0091 | AFR | LWK | RTF1_chr15_41412095_41488563 | RTF1 | chr15 | 41412095 | 41488563 |
| NA21309 | hp2 | a0001 | c0001 | t0005 | g0223 | AFR | LWK | RTF1_chr15_41412095_41488563 | RTF1 | chr15 | 41412095 | 41488563 |
| homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0001 | g0012 | REF | REF | RTF1_chr15_41412095_41488563 | RTF1 | chr15 | 41412095 | 41488563 |
| homoSapiens_grch38 | hp1 | a0001 | c0001 | t0002 | g0102 | REF | REF | RTF1_chr15_41412095_41488563 | RTF1 | chr15 | 41412095 | 41488563 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr15:41417147
|
C | T | 1 | a0002 | 1 | NA18971.hp1 | missense_variant | MODERATE | c.32C>T | p.Ala11Val | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 1/18 | 53/5030 | 32/2133 | 11/710 | chr15 | 41417147 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr15:41417289
|
C | T | 1 | a0001c0006 | 1 | HG03491.hp2 | synonymous_variant | LOW | c.174C>T | p.Ser58Ser | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 1/18 | 195/5030 | 174/2133 | 58/710 | chr15 | 41417289 | ||
| chr15:41438395
|
C | T | 1 | a0001c0002 | 2 | HG02572.hp1 NA20129.hp2 |
synonymous_variant | LOW | c.273C>T | p.Ala91Ala | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 2/18 | 294/5030 | 273/2133 | 91/710 | chr15 | 41438395 | ||
| chr15:41457718
|
T | C | 1 | a0001c0003 | 1 | HG00099.hp1 | synonymous_variant | LOW | c.504T>C | p.Asp168Asp | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 4/18 | 525/5030 | 504/2133 | 168/710 | chr15 | 41457718 | ||
| chr15:41470327
|
G | A | 1 | a0001c0004 | 1 | HG00423.hp1 | synonymous_variant | LOW | c.960G>A | p.Glu320Glu | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 7/18 | 981/5030 | 960/2133 | 320/710 | chr15 | 41470327 | ||
| chr15:41480216
|
T | C | 1 | a0001c0005 | 1 | HG04204.hp1 | splice_region_variant&synonymous_variant | LOW | c.1917T>C | p.Gly639Gly | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 17/18 | 1938/5030 | 1917/2133 | 639/710 | chr15 | 41480216 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr15:41480750
|
T | C | 1 | a0001c0001t0018 | 1 | HG02717.hp1 | 3_prime_UTR_variant | MODIFIER | c.*63T>C | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 18/18 | 63 | chr15 | 41480750 | |||||
| chr15:41480975
|
G | A | 1 | a0001c0001t0019 | 1 | HG04184.hp2 | 3_prime_UTR_variant | MODIFIER | c.*288G>A | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 18/18 | 288 | chr15 | 41480975 | |||||
| chr15:41480977
|
G | A | 1 | a0001c0001t0014 | 2 | HG02572.hp2 HG02615.hp1 |
3_prime_UTR_variant | MODIFIER | c.*290G>A | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 18/18 | 290 | chr15 | 41480977 | |||||
| chr15:41481151
|
G | A | 1 | a0001c0001t0020 | 1 | HG02293.hp2 | 3_prime_UTR_variant | MODIFIER | c.*464G>A | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 18/18 | 464 | chr15 | 41481151 | |||||
| chr15:41481244
|
T | TG | 5 | a0001c0001t0007a0001c0001t0008a0001c0005t0007others(2): Show | 17 | HG00280.hp2 HG00544.hp1 HG01981.hp2 others(14): Show |
3_prime_UTR_variant | MODIFIER | c.*569dupG | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 18/18 | 570 | INFO_REALIGN_3_PRIME | chr15 | 41481244 | ||||
| chr15:41481244
|
TG | T | 11 | a0001c0001t0003a0001c0001t0006a0001c0001t0009others(8): Show | 55 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(52): Show |
3_prime_UTR_variant | MODIFIER | c.*569delG | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 18/18 | 569 | INFO_REALIGN_3_PRIME | chr15 | 41481244 | ||||
| chr15:41481244
|
TGG | T | 5 | a0001c0001t0004a0001c0001t0011a0001c0001t0013others(2): Show | 32 | HG00099.hp1 HG00609.hp1 HG01106.hp1 others(29): Show |
3_prime_UTR_variant | MODIFIER | c.*568_*569delGG | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 18/18 | 568 | INFO_REALIGN_3_PRIME | chr15 | 41481244 | ||||
| chr15:41481244
|
TGGG | T | 1 | a0001c0001t0005 | 15 | HG01081.hp2 HG01106.hp2 HG01257.hp1 others(12): Show |
3_prime_UTR_variant | MODIFIER | c.*567_*569delGGG | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 18/18 | 567 | INFO_REALIGN_3_PRIME | chr15 | 41481244 | ||||
| chr15:41481245
|
G | C | 1 | a0001c0001t0021 | 1 | HG02976.hp2 | 3_prime_UTR_variant | MODIFIER | c.*558G>C | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 18/18 | 558 | chr15 | 41481245 | |||||
| chr15:41481335
|
C | A | 1 | a0001c0001t0017 | 2 | HG03491.hp1 HG03492.hp2 |
3_prime_UTR_variant | MODIFIER | c.*648C>A | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 18/18 | 648 | chr15 | 41481335 | |||||
| chr15:41481543
|
G | T | 6 | a0001c0001t0004a0001c0001t0013a0001c0001t0028others(3): Show | 29 | HG00099.hp1 HG00609.hp1 HG01106.hp1 others(26): Show |
3_prime_UTR_variant | MODIFIER | c.*856G>T | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 18/18 | 856 | chr15 | 41481543 | |||||
| chr15:41481625
|
C | T | 1 | a0001c0001t0025 | 1 | HG02602.hp1 | 3_prime_UTR_variant | MODIFIER | c.*938C>T | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 18/18 | 938 | chr15 | 41481625 | |||||
| chr15:41481738
|
G | C | 1 | a0001c0001t0026 | 1 | HG03834.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1051G>C | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 18/18 | 1051 | chr15 | 41481738 | |||||
| chr15:41481860
|
A | G | 1 | a0001c0001t0030 | 1 | NA19085.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1173A>G | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 18/18 | 1173 | chr15 | 41481860 | |||||
| chr15:41482095
|
G | A | 1 | a0001c0001t0012 | 3 | HG02055.hp2 HG03130.hp1 HG03486.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1408G>A | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 18/18 | 1408 | chr15 | 41482095 | |||||
| chr15:41482225
|
A | G | 26 | a0001c0001t0001a0001c0001t0003a0001c0001t0004others(23): Show | 169 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(166): Show |
3_prime_UTR_variant | MODIFIER | c.*1538A>G | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 18/18 | 1538 | chr15 | 41482225 | |||||
| chr15:41482353
|
G | C | 1 | a0001c0002t0015 | 2 | HG02572.hp1 NA20129.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1666G>C | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 18/18 | 1666 | chr15 | 41482353 | |||||
| chr15:41482892
|
CA | C | 5 | a0001c0001t0003a0001c0001t0012a0001c0001t0016others(2): Show | 34 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(31): Show |
3_prime_UTR_variant | MODIFIER | c.*2206delA | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 18/18 | 2206 | chr15 | 41482892 | |||||
| chr15:41483023
|
C | T | 5 | a0001c0001t0003a0001c0001t0012a0001c0001t0016others(2): Show | 34 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(31): Show |
3_prime_UTR_variant | MODIFIER | c.*2336C>T | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 18/18 | 2336 | chr15 | 41483023 | |||||
| chr15:41483059
|
G | A | 1 | a0001c0001t0022 | 1 | NA19085.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2372G>A | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 18/18 | 2372 | chr15 | 41483059 | |||||
| chr15:41483192
|
G | C | 3 | a0001c0001t0021a0001c0001t0023a0001c0001t0027 | 3 | HG02976.hp2 HG03139.hp1 HG03486.hp1 |
3_prime_UTR_variant | MODIFIER | c.*2505G>C | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 18/18 | 2505 | chr15 | 41483192 | |||||
| chr15:41483247
|
A | G | 1 | a0001c0001t0024 | 1 | NA18943.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2560A>G | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 18/18 | 2560 | chr15 | 41483247 | |||||
| chr15:41483248
|
T | G | 1 | a0001c0001t0010 | 4 | HG01891.hp2 HG02896.hp1 HG03130.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*2561T>G | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 18/18 | 2561 | chr15 | 41483248 | |||||
| chr15:41483350
|
C | G | 2 | a0001c0001t0013a0001c0001t0029 | 4 | NA18955.hp2 NA18968.hp2 NA18971.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*2663C>G | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 18/18 | 2663 | chr15 | 41483350 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr15:41417394
|
G | C | 1 | a0001c0001t0003g0002 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.198+81G>C | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 1/17 | chr15 | 41417394 | ||||||
| chr15:41417716
|
C | G | 1 | a0001c0001t0004g0225 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.198+403C>G | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 1/17 | chr15 | 41417716 | ||||||
| chr15:41417818
|
T | G | 1 | a0001c0001t0002g0003 | 1 | HG01517.hp2 | intron_variant | MODIFIER | c.198+505T>G | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 1/17 | chr15 | 41417818 | ||||||
| chr15:41417957
|
A | G | 15 | a0001c0001t0005g0210a0001c0001t0005g0211a0001c0001t0005g0212others(12): Show | 15 | HG01081.hp2 HG01106.hp2 HG01257.hp1 others(12): Show |
intron_variant | MODIFIER | c.198+644A>G | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 1/17 | chr15 | 41417957 | ||||||
| chr15:41418129
|
T | G | 15 | a0001c0001t0005g0210a0001c0001t0005g0211a0001c0001t0005g0212others(12): Show | 15 | HG01081.hp2 HG01106.hp2 HG01257.hp1 others(12): Show |
intron_variant | MODIFIER | c.198+816T>G | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 1/17 | chr15 | 41418129 | ||||||
| chr15:41418485
|
T | C | 4 | a0001c0001t0005g0210a0001c0001t0005g0211a0001c0001t0005g0212others(1): Show | 4 | HG01891.hp1 HG03041.hp1 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.198+1172T>C | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 1/17 | chr15 | 41418485 | ||||||
| chr15:41418572
|
C | T | 1 | a0001c0001t0014g0209 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.198+1259C>T | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 1/17 | chr15 | 41418572 | ||||||
| chr15:41418632
|
G | T | 1 | a0001c0001t0007g0208 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.198+1319G>T | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 1/17 | chr15 | 41418632 | ||||||
| chr15:41418784
|
C | CA | 15 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0013others(12): Show | 15 | HG01515.hp1 HG01975.hp1 HG02055.hp2 others(12): Show |
intron_variant | MODIFIER | c.198+1488dupA | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr15 | 41418784 | |||||
| chr15:41418784
|
C | CAA | 6 | a0001c0001t0001g0005a0001c0001t0009g0004a0001c0001t0009g0006others(3): Show | 6 | HG01109.hp1 HG01243.hp1 HG02145.hp2 others(3): Show |
intron_variant | MODIFIER | c.198+1487_198+1488d others(4): Show |
RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr15 | 41418784 | |||||
| chr15:41418867
|
T | A | 16 | a0001c0001t0005g0210a0001c0001t0005g0211a0001c0001t0005g0212others(13): Show | 16 | HG01081.hp2 HG01106.hp2 HG01257.hp1 others(13): Show |
intron_variant | MODIFIER | c.198+1554T>A | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 1/17 | chr15 | 41418867 | ||||||
| chr15:41419094
|
A | G | 1 | a0001c0001t0018g0207 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.198+1781A>G | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 1/17 | chr15 | 41419094 | ||||||
| chr15:41419132
|
T | C | 1 | a0001c0001t0003g0002 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.198+1819T>C | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 1/17 | chr15 | 41419132 | ||||||
| chr15:41419186
|
C | T | 1 | a0001c0001t0004g0206 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.198+1873C>T | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 1/17 | chr15 | 41419186 | ||||||
| chr15:41419216
|
T | C | 6 | a0001c0001t0001g0005a0001c0001t0009g0004a0001c0001t0009g0006others(3): Show | 6 | HG01109.hp1 HG01243.hp1 HG02145.hp2 others(3): Show |
intron_variant | MODIFIER | c.198+1903T>C | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 1/17 | chr15 | 41419216 | ||||||
| chr15:41419249
|
C | T | 89 | a0001c0001t0001g0005a0001c0001t0003g0002a0001c0001t0003g0017others(86): Show | 89 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(86): Show |
intron_variant | MODIFIER | c.198+1936C>T | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 1/17 | chr15 | 41419249 | ||||||
| chr15:41419316
|
T | G | 89 | a0001c0001t0001g0005a0001c0001t0003g0002a0001c0001t0003g0017others(86): Show | 89 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(86): Show |
intron_variant | MODIFIER | c.198+2003T>G | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 1/17 | chr15 | 41419316 | ||||||
| chr15:41419493
|
T | A | 1 | a0001c0001t0001g0026 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.198+2180T>A | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 1/17 | chr15 | 41419493 | ||||||
| chr15:41419544
|
A | C | 4 | a0001c0001t0013g0024a0001c0001t0013g0204a0001c0001t0013g0205others(1): Show | 4 | NA18955.hp2 NA18968.hp2 NA18971.hp2 others(1): Show |
intron_variant | MODIFIER | c.198+2231A>C | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 1/17 | chr15 | 41419544 | ||||||
| chr15:41419911
|
C | T | 3 | a0001c0001t0011g0200a0001c0001t0011g0201a0001c0001t0011g0202 | 3 | HG01496.hp1 HG02451.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.198+2598C>T | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 1/17 | chr15 | 41419911 | ||||||
| chr15:41420307
|
T | C | 24 | a0001c0001t0001g0005a0001c0001t0005g0210a0001c0001t0005g0211others(21): Show | 24 | HG01081.hp2 HG01106.hp2 HG01109.hp1 others(21): Show |
intron_variant | MODIFIER | c.198+2994T>C | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 1/17 | chr15 | 41420307 | ||||||
| chr15:41420470
|
C | T | 1 | a0001c0001t0014g0199 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.198+3157C>T | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 1/17 | chr15 | 41420470 | ||||||
| chr15:41420494
|
C | G | 3 | a0001c0001t0021g0148a0001c0001t0023g0146a0001c0001t0027g0147 | 3 | HG02976.hp2 HG03139.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.198+3181C>G | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 1/17 | chr15 | 41420494 | ||||||
| chr15:41420593
|
C | T | 28 | a0001c0001t0004g0177a0001c0001t0004g0178a0001c0001t0004g0179others(25): Show | 28 | HG00099.hp1 HG00609.hp1 HG01106.hp1 others(25): Show |
intron_variant | MODIFIER | c.198+3280C>T | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 1/17 | chr15 | 41420593 | ||||||
| chr15:41420609
|
T | C | 172 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0011others(169): Show | 173 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(170): Show |
intron_variant | MODIFIER | c.198+3296T>C | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 1/17 | chr15 | 41420609 | ||||||
| chr15:41420678
|
T | TTTACCTC others(3): Show |
1 | a0001c0001t0002g0097 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.198+3368_198+3377d others(12): Show |
RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr15 | 41420678 | |||||
| chr15:41420738
|
C | A | 3 | a0001c0001t0006g0098a0001c0001t0006g0099a0001c0001t0006g0100 | 3 | HG00639.hp2 HG00738.hp1 HG03654.hp1 |
intron_variant | MODIFIER | c.198+3425C>A | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 1/17 | chr15 | 41420738 | ||||||
| chr15:41420810
|
G | C | 1 | a0001c0001t0002g0101 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.198+3497G>C | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 1/17 | chr15 | 41420810 | ||||||
| chr15:41420909
|
G | A | 1 | a0001c0001t0014g0199 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.198+3596G>A | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 1/17 | chr15 | 41420909 | ||||||
| chr15:41421021
|
A | G | 55 | a0001c0001t0001g0005a0001c0001t0004g0177a0001c0001t0004g0178others(52): Show | 55 | HG00099.hp1 HG00609.hp1 HG01081.hp2 others(52): Show |
intron_variant | MODIFIER | c.198+3708A>G | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 1/17 | chr15 | 41421021 | ||||||
| chr15:41421028
|
G | A | 1 | a0001c0001t0008g0014 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.198+3715G>A | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 1/17 | chr15 | 41421028 | ||||||
| chr15:41421138
|
A | C | 1 | a0001c0001t0003g0022 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.198+3825A>C | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 1/17 | chr15 | 41421138 | ||||||
| chr15:41421246
|
T | G | 23 | a0001c0001t0003g0017a0001c0001t0003g0018a0001c0001t0003g0019others(20): Show | 23 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(20): Show |
intron_variant | MODIFIER | c.198+3933T>G | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 1/17 | chr15 | 41421246 | ||||||
| chr15:41421434
|
A | C | 224 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0011others(221): Show | 225 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(222): Show |
intron_variant | MODIFIER | c.198+4121A>C | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 1/17 | chr15 | 41421434 | ||||||
| chr15:41421449
|
T | A | 1 | a0001c0001t0001g0026 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.198+4136T>A | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 1/17 | chr15 | 41421449 | ||||||
| chr15:41421456
|
TA | T | 26 | a0001c0001t0004g0179a0001c0001t0004g0181a0001c0001t0004g0182others(23): Show | 26 | HG00099.hp1 HG00609.hp1 HG01106.hp1 others(23): Show |
intron_variant | MODIFIER | c.198+4159delA | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr15 | 41421456 | |||||
| chr15:41421590
|
C | T | 15 | a0001c0001t0005g0210a0001c0001t0005g0211a0001c0001t0005g0212others(12): Show | 15 | HG01081.hp2 HG01106.hp2 HG01257.hp1 others(12): Show |
intron_variant | MODIFIER | c.198+4277C>T | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 1/17 | chr15 | 41421590 | ||||||
| chr15:41421709
|
C | CT | 7 | a0001c0001t0001g0013a0001c0001t0001g0096a0001c0001t0002g0097others(4): Show | 7 | HG01978.hp1 HG02055.hp1 HG03098.hp1 others(4): Show |
intron_variant | MODIFIER | c.198+4413dupT | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr15 | 41421709 | |||||
| chr15:41421793
|
C | T | 1 | a0001c0001t0001g0012 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.198+4480C>T | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 1/17 | chr15 | 41421793 | ||||||
| chr15:41421852
|
A | G | 6 | a0001c0001t0001g0005a0001c0001t0009g0004a0001c0001t0009g0006others(3): Show | 6 | HG01109.hp1 HG01243.hp1 HG02145.hp2 others(3): Show |
intron_variant | MODIFIER | c.198+4539A>G | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 1/17 | chr15 | 41421852 | ||||||
| chr15:41421862
|
C | T | 3 | a0001c0001t0003g0166a0001c0001t0003g0167a0001c0001t0026g0165 | 3 | HG02602.hp2 HG03834.hp2 HG04228.hp1 |
intron_variant | MODIFIER | c.198+4549C>T | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 1/17 | chr15 | 41421862 | ||||||
| chr15:41421866
|
A | G | 3 | a0001c0001t0005g0211a0001c0001t0005g0212a0001c0001t0005g0213 | 3 | HG01891.hp1 HG03041.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.198+4553A>G | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 1/17 | chr15 | 41421866 | ||||||
| chr15:41421874
|
C | T | 33 | a0001c0001t0003g0002a0001c0001t0003g0017a0001c0001t0003g0018others(30): Show | 33 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(30): Show |
intron_variant | MODIFIER | c.198+4561C>T | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 1/17 | chr15 | 41421874 | ||||||
| chr15:41422006
|
C | T | 1 | a0001c0001t0001g0095 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.198+4693C>T | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 1/17 | chr15 | 41422006 | ||||||
| chr15:41422023
|
A | G | 1 | a0001c0006t0008g0144 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.198+4710A>G | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 1/17 | chr15 | 41422023 | ||||||
| chr15:41422023
|
ATTTG | A | 19 | a0001c0001t0001g0027a0001c0001t0001g0029a0001c0001t0001g0030others(16): Show | 19 | HG01081.hp2 HG01106.hp2 HG01257.hp1 others(16): Show |
intron_variant | MODIFIER | c.198+4722_198+4725d others(6): Show |
RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr15 | 41422023 | |||||
| chr15:41422077
|
C | T | 15 | a0001c0001t0005g0210a0001c0001t0005g0211a0001c0001t0005g0212others(12): Show | 15 | HG01081.hp2 HG01106.hp2 HG01257.hp1 others(12): Show |
intron_variant | MODIFIER | c.198+4764C>T | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 1/17 | chr15 | 41422077 | ||||||
| chr15:41422217
|
G | GT | 5 | a0001c0001t0001g0091a0001c0001t0001g0092a0001c0001t0001g0093others(2): Show | 5 | HG01884.hp1 HG02055.hp1 HG02896.hp2 others(2): Show |
intron_variant | MODIFIER | c.198+4905dupT | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr15 | 41422217 | |||||
| chr15:41422223
|
A | G | 4 | a0001c0001t0011g0200a0001c0001t0011g0201a0001c0001t0011g0202others(1): Show | 4 | HG01496.hp1 HG02451.hp2 HG02615.hp1 others(1): Show |
intron_variant | MODIFIER | c.198+4910A>G | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 1/17 | chr15 | 41422223 | ||||||
| chr15:41422305
|
T | C | 1 | a0001c0001t0001g0026 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.198+4992T>C | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 1/17 | chr15 | 41422305 | ||||||
| chr15:41422306
|
A | T | 1 | a0001c0001t0001g0026 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.198+4993A>T | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 1/17 | chr15 | 41422306 | ||||||
| chr15:41422334
|
A | C | 1 | a0001c0001t0001g0026 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.198+5021A>C | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 1/17 | chr15 | 41422334 | ||||||
| chr15:41422401
|
C | A | 1 | a0001c0001t0001g0026 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.198+5088C>A | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 1/17 | chr15 | 41422401 | ||||||
| chr15:41422402
|
A | C | 1 | a0001c0001t0001g0026 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.198+5089A>C | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 1/17 | chr15 | 41422402 | ||||||
| chr15:41422403
|
T | A | 1 | a0001c0001t0001g0026 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.198+5090T>A | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 1/17 | chr15 | 41422403 | ||||||
| chr15:41422498
|
A | T | 1 | a0001c0001t0005g0224 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.198+5185A>T | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 1/17 | chr15 | 41422498 | ||||||
| chr15:41422600
|
A | G | 1 | a0001c0001t0010g0090 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.198+5287A>G | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 1/17 | chr15 | 41422600 | ||||||
| chr15:41422860
|
C | T | 3 | a0001c0001t0005g0211a0001c0001t0005g0212a0001c0001t0005g0213 | 3 | HG01891.hp1 HG03041.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.198+5547C>T | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 1/17 | chr15 | 41422860 | ||||||
| chr15:41422923
|
G | A | 33 | a0001c0001t0003g0002a0001c0001t0003g0017a0001c0001t0003g0018others(30): Show | 33 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(30): Show |
intron_variant | MODIFIER | c.198+5610G>A | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 1/17 | chr15 | 41422923 | ||||||
| chr15:41422935
|
A | G | 28 | a0001c0001t0004g0177a0001c0001t0004g0178a0001c0001t0004g0179others(25): Show | 28 | HG00099.hp1 HG00609.hp1 HG01106.hp1 others(25): Show |
intron_variant | MODIFIER | c.198+5622A>G | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 1/17 | chr15 | 41422935 | ||||||
| chr15:41423213
|
G | A | 1 | a0001c0001t0001g0026 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.198+5900G>A | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 1/17 | chr15 | 41423213 | ||||||
| chr15:41423260
|
G | A | 1 | a0001c0001t0003g0149 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.198+5947G>A | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 1/17 | chr15 | 41423260 | ||||||
| chr15:41423301
|
T | G | 1 | a0001c0001t0001g0026 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.198+5988T>G | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 1/17 | chr15 | 41423301 | ||||||
| chr15:41423302
|
G | C | 1 | a0001c0001t0001g0026 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.198+5989G>C | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 1/17 | chr15 | 41423302 | ||||||
| chr15:41423303
|
C | A | 1 | a0001c0001t0001g0026 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.198+5990C>A | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 1/17 | chr15 | 41423303 | ||||||
| chr15:41423387
|
A | G | 89 | a0001c0001t0001g0005a0001c0001t0003g0002a0001c0001t0003g0017others(86): Show | 89 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(86): Show |
intron_variant | MODIFIER | c.198+6074A>G | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 1/17 | chr15 | 41423387 | ||||||
| chr15:41423426
|
G | A | 1 | a0001c0001t0001g0031 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.198+6113G>A | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 1/17 | chr15 | 41423426 | ||||||
| chr15:41423434
|
A | G | 55 | a0001c0001t0001g0005a0001c0001t0004g0177a0001c0001t0004g0178others(52): Show | 55 | HG00099.hp1 HG00609.hp1 HG01081.hp2 others(52): Show |
intron_variant | MODIFIER | c.198+6121A>G | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 1/17 | chr15 | 41423434 | ||||||
| chr15:41423458
|
C | T | 15 | a0001c0001t0005g0210a0001c0001t0005g0211a0001c0001t0005g0212others(12): Show | 15 | HG01081.hp2 HG01106.hp2 HG01257.hp1 others(12): Show |
intron_variant | MODIFIER | c.198+6145C>T | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 1/17 | chr15 | 41423458 | ||||||
| chr15:41423495
|
G | A | 1 | a0001c0001t0006g0103 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.198+6182G>A | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 1/17 | chr15 | 41423495 | ||||||
| chr15:41423595
|
C | A | 3 | a0001c0001t0011g0200a0001c0001t0011g0201a0001c0001t0011g0202 | 3 | HG01496.hp1 HG02451.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.198+6282C>A | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 1/17 | chr15 | 41423595 | ||||||
| chr15:41423596
|
C | T | 1 | a0001c0001t0003g0164 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.198+6283C>T | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 1/17 | chr15 | 41423596 | ||||||
| chr15:41423610
|
C | T | 2 | a0001c0001t0001g0088a0001c0001t0001g0089 | 2 | HG00741.hp1 HG03654.hp2 |
intron_variant | MODIFIER | c.198+6297C>T | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 1/17 | chr15 | 41423610 | ||||||
| chr15:41423657
|
C | T | 1 | a0001c0001t0007g0087 | 1 | NA19083.hp2 | intron_variant | MODIFIER | c.198+6344C>T | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 1/17 | chr15 | 41423657 | ||||||
| chr15:41423832
|
C | G | 1 | a0001c0001t0001g0086 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.198+6519C>G | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 1/17 | chr15 | 41423832 | ||||||
| chr15:41423838
|
C | T | 1 | a0001c0001t0001g0095 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.198+6525C>T | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 1/17 | chr15 | 41423838 | ||||||
| chr15:41423953
|
A | G | 1 | a0001c0001t0001g0094 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.198+6640A>G | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 1/17 | chr15 | 41423953 | ||||||
| chr15:41424056
|
A | G | 6 | a0001c0001t0001g0005a0001c0001t0009g0004a0001c0001t0009g0006others(3): Show | 6 | HG01109.hp1 HG01243.hp1 HG02145.hp2 others(3): Show |
intron_variant | MODIFIER | c.198+6743A>G | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 1/17 | chr15 | 41424056 | ||||||
| chr15:41424077
|
G | T | 2 | a0001c0001t0014g0199a0001c0001t0014g0209 | 2 | HG02572.hp2 HG02615.hp1 |
intron_variant | MODIFIER | c.198+6764G>T | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 1/17 | chr15 | 41424077 | ||||||
| chr15:41424406
|
A | G | 224 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0011others(221): Show | 225 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(222): Show |
intron_variant | MODIFIER | c.198+7093A>G | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 1/17 | chr15 | 41424406 | ||||||
| chr15:41424836
|
C | T | 1 | a0001c0001t0001g0085 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.198+7523C>T | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 1/17 | chr15 | 41424836 | ||||||
| chr15:41424948
|
G | T | 1 | a0001c0001t0003g0022 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.198+7635G>T | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 1/17 | chr15 | 41424948 | ||||||
| chr15:41425061
|
C | T | 1 | a0001c0001t0009g0084 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.198+7748C>T | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 1/17 | chr15 | 41425061 | ||||||
| chr15:41425115
|
A | T | 23 | a0001c0001t0003g0017a0001c0001t0003g0018a0001c0001t0003g0019others(20): Show | 23 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(20): Show |
intron_variant | MODIFIER | c.198+7802A>T | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 1/17 | chr15 | 41425115 | ||||||
| chr15:41425126
|
G | A | 1 | a0001c0001t0001g0027 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.198+7813G>A | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 1/17 | chr15 | 41425126 | ||||||
| chr15:41425611
|
C | T | 1 | a0001c0001t0005g0223 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.198+8298C>T | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 1/17 | chr15 | 41425611 | ||||||
| chr15:41425940
|
G | A | 2 | a0001c0001t0005g0214a0001c0001t0005g0215 | 2 | HG04199.hp1 NA20905.hp2 |
intron_variant | MODIFIER | c.198+8627G>A | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 1/17 | chr15 | 41425940 | ||||||
| chr15:41425972
|
C | G | 1 | a0001c0001t0002g0143 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.198+8659C>G | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 1/17 | chr15 | 41425972 | ||||||
| chr15:41426134
|
A | T | 3 | a0001c0001t0002g0003a0001c0001t0002g0141a0001c0001t0008g0142 | 3 | HG00280.hp2 HG00323.hp1 HG01517.hp2 |
intron_variant | MODIFIER | c.198+8821A>T | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 1/17 | chr15 | 41426134 | ||||||
| chr15:41426135
|
T | A | 2 | a0001c0001t0008g0104a0001c0002t0015g0032 | 2 | NA19011.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.198+8822T>A | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 1/17 | chr15 | 41426135 | ||||||
| chr15:41426144
|
G | A | 1 | a0001c0001t0016g0150 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.198+8831G>A | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 1/17 | chr15 | 41426144 | ||||||
| chr15:41426312
|
A | AT | 34 | a0001c0001t0001g0005a0001c0001t0004g0177a0001c0001t0004g0178others(31): Show | 34 | HG00099.hp1 HG00609.hp1 HG01106.hp1 others(31): Show |
intron_variant | MODIFIER | c.198+9010dupT | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr15 | 41426312 | |||||
| chr15:41426323
|
T | G | 1 | a0001c0001t0001g0085 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.198+9010T>G | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 1/17 | chr15 | 41426323 | ||||||
| chr15:41426394
|
C | T | 1 | a0001c0001t0002g0097 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.198+9081C>T | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 1/17 | chr15 | 41426394 | ||||||
| chr15:41426395
|
T | C | 1 | a0001c0001t0002g0097 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.198+9082T>C | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 1/17 | chr15 | 41426395 | ||||||
| chr15:41426606
|
T | A | 34 | a0001c0001t0003g0002a0001c0001t0003g0017a0001c0001t0003g0018others(31): Show | 34 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(31): Show |
intron_variant | MODIFIER | c.198+9293T>A | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 1/17 | chr15 | 41426606 | ||||||
| chr15:41426689
|
G | A | 1 | a0001c0001t0009g0028 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.198+9376G>A | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 1/17 | chr15 | 41426689 | ||||||
| chr15:41426690
|
CCCCCCCC others(8): Show |
C | 1 | a0001c0001t0001g0067 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.198+9390_198+9404d others(17): Show |
RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr15 | 41426690 | |||||
| chr15:41426691
|
CCCCCCCC others(7): Show |
C | 3 | a0001c0001t0005g0222a0001c0001t0005g0223a0001c0001t0005g0224 | 3 | HG01517.hp1 HG02976.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.198+9391_198+9404d others(16): Show |
RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr15 | 41426691 | |||||
| chr15:41426692
|
CCCCCCCC others(6): Show |
C | 14 | a0001c0001t0005g0210a0001c0001t0005g0211a0001c0001t0005g0212others(11): Show | 14 | HG01081.hp2 HG01257.hp1 HG01258.hp2 others(11): Show |
intron_variant | MODIFIER | c.198+9395_198+9407d others(15): Show |
RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr15 | 41426692 | |||||
| chr15:41426693
|
CCCCCCCC others(5): Show |
C | 1 | a0001c0001t0005g0216 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.198+9392_198+9403d others(14): Show |
RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr15 | 41426693 | |||||
| chr15:41426694
|
CCCCCCCC others(4): Show |
C | 6 | a0001c0001t0001g0005a0001c0001t0009g0004a0001c0001t0009g0006others(3): Show | 6 | HG01109.hp1 HG01243.hp1 HG02145.hp2 others(3): Show |
intron_variant | MODIFIER | c.198+9392_198+9402d others(13): Show |
RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr15 | 41426694 | |||||
| chr15:41426699
|
C | A | 18 | a0001c0001t0003g0002a0001c0001t0003g0017a0001c0001t0003g0018others(15): Show | 18 | HG00323.hp2 HG00639.hp1 HG01074.hp2 others(15): Show |
intron_variant | MODIFIER | c.198+9386C>A | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 1/17 | chr15 | 41426699 | ||||||
| chr15:41426700
|
C | A | 14 | a0001c0001t0003g0022a0001c0001t0003g0149a0001c0001t0003g0160others(11): Show | 14 | HG00140.hp1 HG00642.hp1 HG00642.hp2 others(11): Show |
intron_variant | MODIFIER | c.198+9387C>A | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 1/17 | chr15 | 41426700 | ||||||
| chr15:41426700
|
C | G | 1 | a0001c0001t0001g0082 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.198+9387C>G | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 1/17 | chr15 | 41426700 | ||||||
| chr15:41426701
|
C | CG | 2 | a0001c0001t0001g0068a0001c0001t0009g0084 | 2 | HG00609.hp2 HG01928.hp1 |
intron_variant | MODIFIER | c.198+9388_198+9389i others(3): Show |
RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 1/17 | chr15 | 41426701 | ||||||
| chr15:41426701
|
C | G | 5 | a0001c0001t0001g0080a0001c0001t0001g0095a0001c0001t0014g0199others(2): Show | 5 | HG02572.hp2 HG02615.hp1 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.198+9388C>G | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 1/17 | chr15 | 41426701 | ||||||
| chr15:41426702
|
C | CG | 6 | a0001c0001t0001g0013a0001c0001t0001g0056a0001c0001t0001g0094others(3): Show | 6 | HG01978.hp2 HG02896.hp2 HG03098.hp1 others(3): Show |
intron_variant | MODIFIER | c.198+9389_198+9390i others(3): Show |
RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 1/17 | chr15 | 41426702 | ||||||
| chr15:41426702
|
C | G | 18 | a0001c0001t0001g0011a0001c0001t0001g0030a0001c0001t0001g0031others(15): Show | 18 | HG01981.hp2 HG02027.hp2 HG02040.hp1 others(15): Show |
intron_variant | MODIFIER | c.198+9389C>G | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 1/17 | chr15 | 41426702 | ||||||
| chr15:41426703
|
C | CG | 15 | a0001c0001t0001g0046a0001c0001t0001g0047a0001c0001t0001g0048others(12): Show | 15 | HG01517.hp2 HG01884.hp2 HG01978.hp1 others(12): Show |
intron_variant | MODIFIER | c.198+9390_198+9391i others(3): Show |
RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 1/17 | chr15 | 41426703 | ||||||
| chr15:41426703
|
C | G | 24 | a0001c0001t0001g0001a0001c0001t0001g0012a0001c0001t0001g0029others(21): Show | 25 | HG00423.hp2 HG00544.hp1 HG01109.hp2 others(22): Show |
intron_variant | MODIFIER | c.198+9390C>G | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 1/17 | chr15 | 41426703 | ||||||
| chr15:41426703
|
CCG | C | 12 | a0001c0001t0001g0076a0001c0001t0001g0077a0001c0001t0001g0078others(9): Show | 12 | HG00642.hp2 HG01975.hp1 HG02040.hp1 others(9): Show |
intron_variant | MODIFIER | c.198+9392_198+9393d others(4): Show |
RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr15 | 41426703 | |||||
| chr15:41426704
|
C | G | 13 | a0001c0001t0001g0050a0001c0001t0001g0051a0001c0001t0001g0053others(10): Show | 13 | HG00558.hp1 HG00558.hp2 HG01074.hp1 others(10): Show |
intron_variant | MODIFIER | c.198+9391C>G | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 1/17 | chr15 | 41426704 | ||||||
| chr15:41426704
|
CG | C | 23 | a0001c0001t0001g0031a0001c0001t0001g0063a0001c0001t0001g0064others(20): Show | 23 | HG00423.hp2 HG00544.hp1 HG00741.hp2 others(20): Show |
intron_variant | MODIFIER | c.198+9392delG | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 1/17 | chr15 | 41426704 | ||||||
| chr15:41426705
|
G | A | 1 | a0001c0001t0003g0163 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.198+9392G>A | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 1/17 | chr15 | 41426705 | ||||||
| chr15:41426705
|
G | C | 114 | a0001c0001t0001g0001a0001c0001t0001g0011a0001c0001t0001g0012others(111): Show | 115 | HG00099.hp1 HG00140.hp2 HG00423.hp1 others(112): Show |
intron_variant | MODIFIER | c.198+9392G>C | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 1/17 | chr15 | 41426705 | ||||||
| chr15:41426705
|
G | GCCCCCCC others(4): Show |
1 | a0001c0001t0013g0024 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.198+9394_198+9404d others(13): Show |
RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr15 | 41426705 | |||||
| chr15:41426707
|
C | G | 6 | a0001c0001t0001g0005a0001c0001t0009g0004a0001c0001t0009g0006others(3): Show | 6 | HG01109.hp1 HG01243.hp1 HG02145.hp2 others(3): Show |
intron_variant | MODIFIER | c.198+9394C>G | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 1/17 | chr15 | 41426707 | ||||||
| chr15:41426708
|
C | A | 2 | a0001c0001t0014g0199a0001c0001t0014g0209 | 2 | HG02572.hp2 HG02615.hp1 |
intron_variant | MODIFIER | c.198+9395C>A | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 1/17 | chr15 | 41426708 | ||||||
| chr15:41426708
|
C | T | 2 | a0001c0001t0001g0044a0001c0001t0024g0045 | 2 | HG02148.hp1 NA18943.hp1 |
intron_variant | MODIFIER | c.198+9395C>T | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 1/17 | chr15 | 41426708 | ||||||
| chr15:41426711
|
C | G | 1 | a0001c0001t0002g0126 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.198+9398C>G | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 1/17 | chr15 | 41426711 | ||||||
| chr15:41426712
|
C | G | 1 | a0001c0001t0014g0199 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.198+9399C>G | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 1/17 | chr15 | 41426712 | ||||||
| chr15:41426713
|
C | A | 1 | a0001c0001t0011g0023 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.198+9400C>A | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 1/17 | chr15 | 41426713 | ||||||
| chr15:41426715
|
C | G | 1 | a0001c0001t0002g0136 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.198+9402C>G | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 1/17 | chr15 | 41426715 | ||||||
| chr15:41426774
|
CAT | C | 11 | a0001c0001t0003g0002a0001c0001t0003g0173a0001c0001t0003g0174others(8): Show | 11 | HG00642.hp2 HG01081.hp2 HG01106.hp2 others(8): Show |
intron_variant | MODIFIER | c.198+9468_198+9469d others(4): Show |
RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr15 | 41426774 | |||||
| chr15:41426778
|
T | C | 1 | a0001c0001t0002g0115 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.198+9465T>C | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 1/17 | chr15 | 41426778 | ||||||
| chr15:41426779
|
A | ATG | 2 | a0001c0001t0003g0159a0001c0001t0003g0167 | 2 | HG01081.hp1 HG04228.hp1 |
intron_variant | MODIFIER | c.198+9467_198+9468i others(4): Show |
RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr15 | 41426779 | |||||
| chr15:41426779
|
A | ATGTG | 2 | a0001c0001t0001g0027a0001c0001t0006g0140 | 2 | HG01168.hp2 HG02145.hp1 |
intron_variant | MODIFIER | c.198+9467_198+9468i others(6): Show |
RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr15 | 41426779 | |||||
| chr15:41426779
|
ATATG | A | 22 | a0001c0001t0003g0017a0001c0001t0003g0019a0001c0001t0003g0020others(19): Show | 22 | HG00099.hp2 HG00140.hp1 HG00639.hp1 others(19): Show |
intron_variant | MODIFIER | c.198+9468_198+9471d others(6): Show |
RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr15 | 41426779 | |||||
| chr15:41426779
|
ATATGTG | A | 8 | a0001c0001t0003g0018a0001c0001t0003g0164a0001c0001t0003g0169others(5): Show | 8 | HG00323.hp2 HG01515.hp1 HG02055.hp2 others(5): Show |
intron_variant | MODIFIER | c.198+9468_198+9473d others(8): Show |
RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr15 | 41426779 | |||||
| chr15:41426779
|
ATATGTGT others(11): Show |
A | 2 | a0001c0001t0005g0214a0001c0001t0005g0215 | 2 | HG04199.hp1 NA20905.hp2 |
intron_variant | MODIFIER | c.198+9468_198+9485d others(20): Show |
RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr15 | 41426779 | |||||
| chr15:41426779
|
ATATGTGT others(13): Show |
A | 1 | a0001c0001t0005g0211 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.198+9468_198+9487d others(22): Show |
RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr15 | 41426779 | |||||
| chr15:41426781
|
A | ATG | 58 | a0001c0001t0001g0001a0001c0001t0001g0013a0001c0001t0001g0029others(55): Show | 59 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(56): Show |
intron_variant | MODIFIER | c.198+9512_198+9513d others(4): Show |
RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr15 | 41426781 | |||||
| chr15:41426781
|
A | ATGTG | 33 | a0001c0001t0001g0037a0001c0001t0001g0042a0001c0001t0001g0043others(30): Show | 33 | HG00099.hp1 HG00544.hp1 HG01106.hp1 others(30): Show |
intron_variant | MODIFIER | c.198+9510_198+9513d others(6): Show |
RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr15 | 41426781 | |||||
| chr15:41426781
|
A | ATGTGTG | 9 | a0001c0001t0001g0026a0001c0001t0002g0015a0001c0001t0002g0123others(6): Show | 9 | HG00280.hp1 HG00609.hp1 HG00639.hp2 others(6): Show |
intron_variant | MODIFIER | c.198+9508_198+9513d others(8): Show |
RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr15 | 41426781 | |||||
| chr15:41426781
|
A | ATGTGTGT others(1): Show |
6 | a0001c0001t0001g0011a0001c0001t0002g0097a0001c0001t0002g0135others(3): Show | 6 | HG01978.hp1 HG02698.hp2 HG02717.hp1 others(3): Show |
intron_variant | MODIFIER | c.198+9506_198+9513d others(10): Show |
RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr15 | 41426781 | |||||
| chr15:41426781
|
A | ATGTGTGT others(3): Show |
4 | a0001c0001t0001g0031a0001c0001t0002g0145a0001c0001t0004g0197others(1): Show | 4 | HG02027.hp2 HG02165.hp2 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.198+9504_198+9513d others(12): Show |
RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr15 | 41426781 | |||||
| chr15:41426781
|
A | ATGTGTGT others(9): Show |
1 | a0001c0001t0004g0206 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.198+9498_198+9513d others(18): Show |
RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr15 | 41426781 | |||||
| chr15:41426781
|
A | G | 7 | a0001c0001t0001g0027a0001c0001t0003g0159a0001c0001t0003g0167others(4): Show | 7 | HG00544.hp2 HG01081.hp1 HG01168.hp2 others(4): Show |
intron_variant | MODIFIER | c.198+9468A>G | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 1/17 | chr15 | 41426781 | ||||||
| chr15:41426781
|
ATG | A | 10 | a0001c0001t0001g0044a0001c0001t0001g0076a0001c0001t0001g0091others(7): Show | 10 | HG01496.hp1 HG01884.hp1 HG02055.hp1 others(7): Show |
intron_variant | MODIFIER | c.198+9512_198+9513d others(4): Show |
RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr15 | 41426781 | |||||
| chr15:41426781
|
ATGTG | A | 10 | a0001c0001t0001g0005a0001c0001t0001g0088a0001c0001t0001g0089others(7): Show | 10 | HG00741.hp1 HG01109.hp1 HG01243.hp1 others(7): Show |
intron_variant | MODIFIER | c.198+9510_198+9513d others(6): Show |
RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr15 | 41426781 | |||||
| chr15:41426781
|
ATGTGTGT others(3): Show |
A | 4 | a0001c0001t0001g0094a0001c0001t0006g0105a0001c0001t0014g0199others(1): Show | 4 | HG02293.hp2 HG02615.hp1 HG02896.hp2 others(1): Show |
intron_variant | MODIFIER | c.198+9504_198+9513d others(12): Show |
RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr15 | 41426781 | |||||
| chr15:41426781
|
ATGTGTGT others(9): Show |
A | 1 | a0001c0001t0003g0022 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.198+9498_198+9513d others(18): Show |
RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr15 | 41426781 | |||||
| chr15:41426781
|
ATGTGTGT others(15): Show |
A | 1 | a0001c0001t0011g0023 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.198+9492_198+9513d others(24): Show |
RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr15 | 41426781 | |||||
| chr15:41426815
|
G | T | 1 | a0001c0001t0014g0209 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.198+9502G>T | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 1/17 | chr15 | 41426815 | ||||||
| chr15:41426830
|
TTTTGTTT others(5): Show |
T | 1 | a0001c0001t0014g0209 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.198+9533_198+9544d others(14): Show |
RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr15 | 41426830 | |||||
| chr15:41426873
|
A | G | 15 | a0001c0001t0005g0210a0001c0001t0005g0211a0001c0001t0005g0212others(12): Show | 15 | HG01081.hp2 HG01106.hp2 HG01257.hp1 others(12): Show |
intron_variant | MODIFIER | c.198+9560A>G | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 1/17 | chr15 | 41426873 | ||||||
| chr15:41427145
|
A | AT | 8 | a0001c0001t0001g0027a0001c0001t0001g0076a0001c0001t0002g0113others(5): Show | 8 | HG00544.hp2 HG01891.hp2 HG02145.hp1 others(5): Show |
intron_variant | MODIFIER | c.198+9856dupT | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr15 | 41427145 | |||||
| chr15:41427145
|
AT | A | 60 | a0001c0001t0001g0001a0001c0001t0001g0012a0001c0001t0001g0026others(57): Show | 61 | HG00323.hp1 HG00423.hp2 HG00544.hp1 others(58): Show |
intron_variant | MODIFIER | c.198+9856delT | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr15 | 41427145 | |||||
| chr15:41427145
|
ATT | A | 37 | a0001c0001t0001g0038a0001c0001t0001g0063a0001c0001t0001g0064others(34): Show | 37 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(34): Show |
intron_variant | MODIFIER | c.198+9855_198+9856d others(4): Show |
RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr15 | 41427145 | |||||
| chr15:41427145
|
ATTT | A | 52 | a0001c0001t0001g0005a0001c0001t0003g0002a0001c0001t0004g0177others(49): Show | 52 | HG00099.hp1 HG01081.hp2 HG01106.hp1 others(49): Show |
intron_variant | MODIFIER | c.198+9854_198+9856d others(5): Show |
RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr15 | 41427145 | |||||
| chr15:41427183
|
G | T | 1 | a0001c0001t0001g0041 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.198+9870G>T | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 1/17 | chr15 | 41427183 | ||||||
| chr15:41427301
|
G | A | 6 | a0001c0001t0001g0005a0001c0001t0009g0004a0001c0001t0009g0006others(3): Show | 6 | HG01109.hp1 HG01243.hp1 HG02145.hp2 others(3): Show |
intron_variant | MODIFIER | c.198+9988G>A | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 1/17 | chr15 | 41427301 | ||||||
| chr15:41427446
|
C | T | 2 | a0001c0001t0004g0177a0001c0001t0004g0186 | 2 | HG02027.hp1 NA19063.hp1 |
intron_variant | MODIFIER | c.198+10133C>T | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 1/17 | chr15 | 41427446 | ||||||
| chr15:41427508
|
A | G | 23 | a0001c0001t0003g0017a0001c0001t0003g0018a0001c0001t0003g0019others(20): Show | 23 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(20): Show |
intron_variant | MODIFIER | c.198+10195A>G | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 1/17 | chr15 | 41427508 | ||||||
| chr15:41427669
|
C | A | 1 | a0001c0001t0004g0178 | 1 | NA18961.hp2 | intron_variant | MODIFIER | c.198+10356C>A | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 1/17 | chr15 | 41427669 | ||||||
| chr15:41427749
|
T | C | 1 | a0001c0001t0007g0072 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.198+10436T>C | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 1/17 | chr15 | 41427749 | ||||||
| chr15:41427880
|
G | A | 2 | a0001c0001t0001g0092a0001c0001t0001g0096 | 2 | HG01884.hp1 HG02055.hp1 |
intron_variant | MODIFIER | c.199-10441G>A | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 1/17 | chr15 | 41427880 | ||||||
| chr15:41428092
|
C | CTTTTTTT others(322): Show |
1 | a0001c0001t0011g0023 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.199-10219_199-1021 others(333): Show |
RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr15 | 41428092 | |||||
| chr15:41428257
|
C | CT | 24 | a0001c0001t0001g0027a0001c0001t0001g0031a0001c0001t0001g0033others(21): Show | 24 | HG00609.hp2 HG00741.hp1 HG01081.hp2 others(21): Show |
intron_variant | MODIFIER | c.199-10036dupT | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr15 | 41428257 | |||||
| chr15:41428257
|
C | CTT | 11 | a0001c0001t0005g0210a0001c0001t0005g0211a0001c0001t0005g0213others(8): Show | 11 | HG01106.hp2 HG01257.hp1 HG01258.hp2 others(8): Show |
intron_variant | MODIFIER | c.199-10037_199-1003 others(6): Show |
RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr15 | 41428257 | |||||
| chr15:41428257
|
CT | C | 13 | a0001c0001t0001g0005a0001c0001t0001g0106a0001c0001t0002g0003others(10): Show | 13 | HG00280.hp1 HG01109.hp1 HG01243.hp1 others(10): Show |
intron_variant | MODIFIER | c.199-10036delT | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr15 | 41428257 | |||||
| chr15:41428257
|
CTT | C | 25 | a0001c0001t0004g0177a0001c0001t0004g0178a0001c0001t0004g0179others(22): Show | 25 | HG00099.hp1 HG00609.hp1 HG01106.hp1 others(22): Show |
intron_variant | MODIFIER | c.199-10037_199-1003 others(6): Show |
RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr15 | 41428257 | |||||
| chr15:41428257
|
CTTTTTTT others(3): Show |
C | 30 | a0001c0001t0003g0002a0001c0001t0003g0017a0001c0001t0003g0018others(27): Show | 30 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(27): Show |
intron_variant | MODIFIER | c.199-10045_199-1003 others(14): Show |
RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr15 | 41428257 | |||||
| chr15:41428257
|
CTTTTTTT others(4): Show |
C | 2 | a0001c0001t0017g0152a0001c0001t0026g0165 | 2 | HG03491.hp1 HG03834.hp2 |
intron_variant | MODIFIER | c.199-10046_199-1003 others(15): Show |
RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr15 | 41428257 | |||||
| chr15:41428345
|
G | T | 28 | a0001c0001t0004g0177a0001c0001t0004g0178a0001c0001t0004g0179others(25): Show | 28 | HG00099.hp1 HG00609.hp1 HG01106.hp1 others(25): Show |
intron_variant | MODIFIER | c.199-9976G>T | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 1/17 | chr15 | 41428345 | ||||||
| chr15:41428376
|
T | TC | 6 | a0001c0001t0001g0005a0001c0001t0009g0004a0001c0001t0009g0006others(3): Show | 6 | HG01109.hp1 HG01243.hp1 HG02145.hp2 others(3): Show |
intron_variant | MODIFIER | c.199-9942dupC | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr15 | 41428376 | |||||
| chr15:41428390
|
C | T | 1 | a0001c0001t0013g0205 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.199-9931C>T | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 1/17 | chr15 | 41428390 | ||||||
| chr15:41428546
|
G | C | 6 | a0001c0001t0001g0005a0001c0001t0009g0004a0001c0001t0009g0006others(3): Show | 6 | HG01109.hp1 HG01243.hp1 HG02145.hp2 others(3): Show |
intron_variant | MODIFIER | c.199-9775G>C | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 1/17 | chr15 | 41428546 | ||||||
| chr15:41428557
|
C | G | 1 | a0001c0001t0004g0191 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.199-9764C>G | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 1/17 | chr15 | 41428557 | ||||||
| chr15:41428844
|
G | A | 89 | a0001c0001t0001g0005a0001c0001t0003g0002a0001c0001t0003g0017others(86): Show | 89 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(86): Show |
intron_variant | MODIFIER | c.199-9477G>A | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 1/17 | chr15 | 41428844 | ||||||
| chr15:41429217
|
A | G | 1 | a0001c0001t0021g0148 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.199-9104A>G | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 1/17 | chr15 | 41429217 | ||||||
| chr15:41429518
|
A | G | 1 | a0001c0001t0002g0015 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.199-8803A>G | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 1/17 | chr15 | 41429518 | ||||||
| chr15:41429590
|
T | G | 55 | a0001c0001t0001g0005a0001c0001t0004g0177a0001c0001t0004g0178others(52): Show | 55 | HG00099.hp1 HG00609.hp1 HG01081.hp2 others(52): Show |
intron_variant | MODIFIER | c.199-8731T>G | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 1/17 | chr15 | 41429590 | ||||||
| chr15:41429613
|
C | T | 2 | a0001c0002t0015g0032a0001c0002t0015g0057 | 2 | HG02572.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.199-8708C>T | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 1/17 | chr15 | 41429613 | ||||||
| chr15:41429637
|
G | C | 15 | a0001c0001t0005g0210a0001c0001t0005g0211a0001c0001t0005g0212others(12): Show | 15 | HG01081.hp2 HG01106.hp2 HG01257.hp1 others(12): Show |
intron_variant | MODIFIER | c.199-8684G>C | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 1/17 | chr15 | 41429637 | ||||||
| chr15:41429672
|
T | C | 1 | a0001c0001t0001g0027 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.199-8649T>C | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 1/17 | chr15 | 41429672 | ||||||
| chr15:41429743
|
T | G | 1 | a0001c0001t0003g0022 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.199-8578T>G | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 1/17 | chr15 | 41429743 | ||||||
| chr15:41429786
|
G | A | 1 | a0001c0001t0003g0022 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.199-8535G>A | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 1/17 | chr15 | 41429786 | ||||||
| chr15:41429827
|
C | G | 3 | a0001c0001t0011g0023a0001c0001t0014g0199a0001c0001t0014g0209 | 3 | HG02572.hp2 HG02615.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.199-8494C>G | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 1/17 | chr15 | 41429827 | ||||||
| chr15:41430009
|
T | TTTTCTTT others(306): Show |
1 | a0001c0001t0004g0179 | 1 | NA18949.hp1 | intron_variant | MODIFIER | c.199-8311_199-8310i others(315): Show |
RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr15 | 41430009 | |||||
| chr15:41430009
|
T | TTTTTTTT others(306): Show |
1 | a0001c0001t0013g0205 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.199-8311_199-8310i others(315): Show |
RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr15 | 41430009 | |||||
| chr15:41430010
|
T | TTTTTTTT others(298): Show |
1 | a0001c0001t0004g0188 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.199-8311_199-8310i others(307): Show |
RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 1/17 | chr15 | 41430010 | ||||||
| chr15:41430010
|
T | TTTTTTTT others(302): Show |
1 | a0001c0001t0004g0198 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.199-8311_199-8310i others(311): Show |
RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 1/17 | chr15 | 41430010 | ||||||
| chr15:41430010
|
T | TTTTTTTT others(303): Show |
16 | a0001c0001t0004g0177a0001c0001t0004g0181a0001c0001t0004g0183others(13): Show | 16 | HG00609.hp1 HG01928.hp2 HG02004.hp2 others(13): Show |
intron_variant | MODIFIER | c.199-8311_199-8310i others(312): Show |
RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 1/17 | chr15 | 41430010 | ||||||
| chr15:41430010
|
T | TTTTTTTT others(304): Show |
6 | a0001c0001t0004g0182a0001c0001t0004g0191a0001c0001t0004g0192others(3): Show | 6 | HG00099.hp1 HG01981.hp1 HG02486.hp2 others(3): Show |
intron_variant | MODIFIER | c.199-8311_199-8310i others(313): Show |
RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 1/17 | chr15 | 41430010 | ||||||
| chr15:41430010
|
T | TTTTTTTT others(304): Show |
1 | a0001c0001t0004g0186 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.199-8311_199-8310i others(313): Show |
RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 1/17 | chr15 | 41430010 | ||||||
| chr15:41430010
|
T | TTTTTTTT others(305): Show |
1 | a0001c0001t0004g0178 | 1 | NA18961.hp2 | intron_variant | MODIFIER | c.199-8311_199-8310i others(314): Show |
RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 1/17 | chr15 | 41430010 | ||||||
| chr15:41430011
|
C | T | 28 | a0001c0001t0004g0177a0001c0001t0004g0178a0001c0001t0004g0179others(25): Show | 28 | HG00099.hp1 HG00609.hp1 HG01106.hp1 others(25): Show |
intron_variant | MODIFIER | c.199-8310C>T | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 1/17 | chr15 | 41430011 | ||||||
| chr15:41430011
|
CT | C | 8 | a0001c0001t0001g0005a0001c0001t0001g0026a0001c0001t0002g0123others(5): Show | 8 | HG01109.hp1 HG01243.hp1 HG02145.hp2 others(5): Show |
intron_variant | MODIFIER | c.199-8296delT | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr15 | 41430011 | |||||
| chr15:41430044
|
A | G | 18 | a0001c0001t0003g0017a0001c0001t0003g0018a0001c0001t0003g0020others(15): Show | 18 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(15): Show |
intron_variant | MODIFIER | c.199-8277A>G | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 1/17 | chr15 | 41430044 | ||||||
| chr15:41430106
|
C | T | 28 | a0001c0001t0004g0177a0001c0001t0004g0178a0001c0001t0004g0179others(25): Show | 28 | HG00099.hp1 HG00609.hp1 HG01106.hp1 others(25): Show |
intron_variant | MODIFIER | c.199-8215C>T | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 1/17 | chr15 | 41430106 | ||||||
| chr15:41430117
|
C | T | 1 | a0001c0001t0007g0075 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.199-8204C>T | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 1/17 | chr15 | 41430117 | ||||||
| chr15:41430174
|
A | AT | 29 | a0001c0001t0001g0037a0001c0001t0001g0044a0001c0001t0001g0088others(26): Show | 29 | HG00609.hp2 HG00741.hp1 HG01081.hp2 others(26): Show |
intron_variant | MODIFIER | c.199-8125dupT | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr15 | 41430174 | |||||
| chr15:41430226
|
G | A | 14 | a0001c0001t0005g0210a0001c0001t0005g0211a0001c0001t0005g0212others(11): Show | 14 | HG01081.hp2 HG01106.hp2 HG01257.hp1 others(11): Show |
intron_variant | MODIFIER | c.199-8095G>A | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 1/17 | chr15 | 41430226 | ||||||
| chr15:41430286
|
C | T | 3 | a0001c0001t0011g0023a0001c0001t0014g0199a0001c0001t0014g0209 | 3 | HG02572.hp2 HG02615.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.199-8035C>T | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 1/17 | chr15 | 41430286 | ||||||
| chr15:41430296
|
C | T | 1 | a0001c0001t0003g0169 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.199-8025C>T | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 1/17 | chr15 | 41430296 | ||||||
| chr15:41430297
|
G | A | 6 | a0001c0001t0004g0193a0001c0001t0004g0194a0001c0001t0004g0195others(3): Show | 6 | HG00609.hp1 HG02165.hp2 NA18943.hp2 others(3): Show |
intron_variant | MODIFIER | c.199-8024G>A | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 1/17 | chr15 | 41430297 | ||||||
| chr15:41430405
|
T | C | 1 | a0001c0002t0015g0032 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.199-7916T>C | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 1/17 | chr15 | 41430405 | ||||||
| chr15:41430585
|
C | T | 1 | a0001c0001t0011g0023 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.199-7736C>T | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 1/17 | chr15 | 41430585 | ||||||
| chr15:41430655
|
C | T | 28 | a0001c0001t0004g0177a0001c0001t0004g0178a0001c0001t0004g0179others(25): Show | 28 | HG00099.hp1 HG00609.hp1 HG01106.hp1 others(25): Show |
intron_variant | MODIFIER | c.199-7666C>T | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 1/17 | chr15 | 41430655 | ||||||
| chr15:41430680
|
G | A | 1 | a0001c0001t0002g0097 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.199-7641G>A | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 1/17 | chr15 | 41430680 | ||||||
| chr15:41430969
|
C | T | 28 | a0001c0001t0004g0177a0001c0001t0004g0178a0001c0001t0004g0179others(25): Show | 28 | HG00099.hp1 HG00609.hp1 HG01106.hp1 others(25): Show |
intron_variant | MODIFIER | c.199-7352C>T | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 1/17 | chr15 | 41430969 | ||||||
| chr15:41431218
|
C | CT | 31 | a0001c0001t0001g0031a0001c0001t0002g0097a0001c0001t0004g0177others(28): Show | 31 | HG00099.hp1 HG00609.hp1 HG01106.hp1 others(28): Show |
intron_variant | MODIFIER | c.199-7090dupT | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr15 | 41431218 | |||||
| chr15:41431371
|
C | T | 4 | a0001c0001t0001g0117a0001c0001t0002g0114a0001c0001t0002g0128others(1): Show | 4 | HG00423.hp1 HG02040.hp2 NA18949.hp2 others(1): Show |
intron_variant | MODIFIER | c.199-6950C>T | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 1/17 | chr15 | 41431371 | ||||||
| chr15:41431634
|
A | G | 1 | a0001c0001t0003g0151 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.199-6687A>G | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 1/17 | chr15 | 41431634 | ||||||
| chr15:41431638
|
T | G | 1 | a0001c0001t0011g0023 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.199-6683T>G | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 1/17 | chr15 | 41431638 | ||||||
| chr15:41431687
|
C | T | 1 | a0001c0001t0009g0008 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.199-6634C>T | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 1/17 | chr15 | 41431687 | ||||||
| chr15:41431803
|
C | CT | 7 | a0001c0001t0001g0005a0001c0001t0001g0036a0001c0001t0009g0004others(4): Show | 7 | HG00140.hp2 HG01109.hp1 HG01243.hp1 others(4): Show |
intron_variant | MODIFIER | c.199-6503dupT | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr15 | 41431803 | |||||
| chr15:41431926
|
G | A | 1 | a0001c0001t0001g0033 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.199-6395G>A | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 1/17 | chr15 | 41431926 | ||||||
| chr15:41431948
|
C | T | 3 | a0001c0001t0011g0200a0001c0001t0011g0201a0001c0001t0011g0202 | 3 | HG01496.hp1 HG02451.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.199-6373C>T | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 1/17 | chr15 | 41431948 | ||||||
| chr15:41431990
|
G | A | 23 | a0001c0001t0003g0017a0001c0001t0003g0018a0001c0001t0003g0019others(20): Show | 23 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(20): Show |
intron_variant | MODIFIER | c.199-6331G>A | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 1/17 | chr15 | 41431990 | ||||||
| chr15:41432185
|
T | C | 1 | a0001c0001t0007g0075 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.199-6136T>C | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 1/17 | chr15 | 41432185 | ||||||
| chr15:41432196
|
C | CT | 10 | a0001c0001t0003g0022a0001c0001t0004g0179a0001c0001t0005g0214others(7): Show | 10 | HG00639.hp2 HG00738.hp1 HG01496.hp1 others(7): Show |
intron_variant | MODIFIER | c.199-6110dupT | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr15 | 41432196 | |||||
| chr15:41432321
|
C | T | 1 | a0001c0001t0003g0022 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.199-6000C>T | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 1/17 | chr15 | 41432321 | ||||||
| chr15:41432355
|
G | A | 3 | a0001c0001t0011g0023a0001c0001t0014g0199a0001c0001t0014g0209 | 3 | HG02572.hp2 HG02615.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.199-5966G>A | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 1/17 | chr15 | 41432355 | ||||||
| chr15:41432420
|
A | G | 6 | a0001c0001t0001g0005a0001c0001t0009g0004a0001c0001t0009g0006others(3): Show | 6 | HG01109.hp1 HG01243.hp1 HG02145.hp2 others(3): Show |
intron_variant | MODIFIER | c.199-5901A>G | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 1/17 | chr15 | 41432420 | ||||||
| chr15:41432444
|
A | G | 24 | a0001c0001t0001g0005a0001c0001t0005g0210a0001c0001t0005g0211others(21): Show | 24 | HG01081.hp2 HG01106.hp2 HG01109.hp1 others(21): Show |
intron_variant | MODIFIER | c.199-5877A>G | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 1/17 | chr15 | 41432444 | ||||||
| chr15:41432492
|
C | T | 28 | a0001c0001t0004g0177a0001c0001t0004g0178a0001c0001t0004g0179others(25): Show | 28 | HG00099.hp1 HG00609.hp1 HG01106.hp1 others(25): Show |
intron_variant | MODIFIER | c.199-5829C>T | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 1/17 | chr15 | 41432492 | ||||||
| chr15:41432583
|
A | T | 6 | a0001c0001t0001g0005a0001c0001t0009g0004a0001c0001t0009g0006others(3): Show | 6 | HG01109.hp1 HG01243.hp1 HG02145.hp2 others(3): Show |
intron_variant | MODIFIER | c.199-5738A>T | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 1/17 | chr15 | 41432583 | ||||||
| chr15:41432707
|
G | A | 6 | a0001c0001t0001g0005a0001c0001t0009g0004a0001c0001t0009g0006others(3): Show | 6 | HG01109.hp1 HG01243.hp1 HG02145.hp2 others(3): Show |
intron_variant | MODIFIER | c.199-5614G>A | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 1/17 | chr15 | 41432707 | ||||||
| chr15:41432825
|
G | A | 33 | a0001c0001t0003g0002a0001c0001t0003g0017a0001c0001t0003g0018others(30): Show | 33 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(30): Show |
intron_variant | MODIFIER | c.199-5496G>A | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 1/17 | chr15 | 41432825 | ||||||
| chr15:41432863
|
A | G | 215 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0011others(212): Show | 216 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(213): Show |
intron_variant | MODIFIER | c.199-5458A>G | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 1/17 | chr15 | 41432863 | ||||||
| chr15:41432876
|
T | G | 1 | a0001c0001t0003g0019 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.199-5445T>G | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 1/17 | chr15 | 41432876 | ||||||
| chr15:41432885
|
C | G | 1 | a0001c0001t0003g0022 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.199-5436C>G | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 1/17 | chr15 | 41432885 | ||||||
| chr15:41432969
|
G | A | 24 | a0001c0001t0001g0005a0001c0001t0005g0210a0001c0001t0005g0211others(21): Show | 24 | HG01081.hp2 HG01106.hp2 HG01109.hp1 others(21): Show |
intron_variant | MODIFIER | c.199-5352G>A | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 1/17 | chr15 | 41432969 | ||||||
| chr15:41432980
|
C | T | 2 | a0001c0001t0014g0199a0001c0001t0014g0209 | 2 | HG02572.hp2 HG02615.hp1 |
intron_variant | MODIFIER | c.199-5341C>T | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 1/17 | chr15 | 41432980 | ||||||
| chr15:41433169
|
A | G | 28 | a0001c0001t0004g0177a0001c0001t0004g0178a0001c0001t0004g0179others(25): Show | 28 | HG00099.hp1 HG00609.hp1 HG01106.hp1 others(25): Show |
intron_variant | MODIFIER | c.199-5152A>G | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 1/17 | chr15 | 41433169 | ||||||
| chr15:41433196
|
C | T | 2 | a0001c0001t0012g0171a0001c0001t0014g0209 | 2 | HG02572.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.199-5125C>T | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 1/17 | chr15 | 41433196 | ||||||
| chr15:41433221
|
C | T | 5 | a0001c0001t0001g0091a0001c0001t0001g0092a0001c0001t0001g0093others(2): Show | 5 | HG01884.hp1 HG02055.hp1 HG02896.hp2 others(2): Show |
intron_variant | MODIFIER | c.199-5100C>T | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 1/17 | chr15 | 41433221 | ||||||
| chr15:41433256
|
T | A | 1 | a0001c0001t0005g0223 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.199-5065T>A | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 1/17 | chr15 | 41433256 | ||||||
| chr15:41433323
|
T | C | 1 | a0001c0001t0001g0068 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.199-4998T>C | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 1/17 | chr15 | 41433323 | ||||||
| chr15:41433369
|
C | G | 5 | a0001c0001t0003g0019a0001c0001t0003g0166a0001c0001t0003g0167others(2): Show | 5 | HG02602.hp2 HG03834.hp2 HG04184.hp1 others(2): Show |
intron_variant | MODIFIER | c.199-4952C>G | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 1/17 | chr15 | 41433369 | ||||||
| chr15:41433407
|
T | A | 1 | a0001c0001t0007g0208 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.199-4914T>A | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 1/17 | chr15 | 41433407 | ||||||
| chr15:41433459
|
T | C | 6 | a0001c0001t0001g0005a0001c0001t0009g0004a0001c0001t0009g0006others(3): Show | 6 | HG01109.hp1 HG01243.hp1 HG02145.hp2 others(3): Show |
intron_variant | MODIFIER | c.199-4862T>C | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 1/17 | chr15 | 41433459 | ||||||
| chr15:41433479
|
C | T | 28 | a0001c0001t0004g0177a0001c0001t0004g0178a0001c0001t0004g0179others(25): Show | 28 | HG00099.hp1 HG00609.hp1 HG01106.hp1 others(25): Show |
intron_variant | MODIFIER | c.199-4842C>T | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 1/17 | chr15 | 41433479 | ||||||
| chr15:41433598
|
A | G | 28 | a0001c0001t0004g0177a0001c0001t0004g0178a0001c0001t0004g0179others(25): Show | 28 | HG00099.hp1 HG00609.hp1 HG01106.hp1 others(25): Show |
intron_variant | MODIFIER | c.199-4723A>G | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 1/17 | chr15 | 41433598 | ||||||
| chr15:41433843
|
C | CT | 11 | a0001c0001t0001g0027a0001c0001t0001g0040a0001c0001t0001g0068others(8): Show | 11 | HG01928.hp1 HG02145.hp1 HG02293.hp2 others(8): Show |
intron_variant | MODIFIER | c.199-4457dupT | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr15 | 41433843 | |||||
| chr15:41433843
|
CT | C | 21 | a0001c0001t0001g0005a0001c0001t0001g0069a0001c0001t0002g0137others(18): Show | 21 | HG00099.hp1 HG01081.hp1 HG01109.hp1 others(18): Show |
intron_variant | MODIFIER | c.199-4457delT | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr15 | 41433843 | |||||
| chr15:41433843
|
CTT | C | 14 | a0001c0001t0005g0210a0001c0001t0005g0211a0001c0001t0005g0212others(11): Show | 14 | HG01081.hp2 HG01106.hp2 HG01257.hp1 others(11): Show |
intron_variant | MODIFIER | c.199-4458_199-4457d others(4): Show |
RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr15 | 41433843 | |||||
| chr15:41433912
|
T | C | 1 | a0001c0001t0023g0146 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.199-4409T>C | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 1/17 | chr15 | 41433912 | ||||||
| chr15:41434135
|
A | G | 24 | a0001c0001t0001g0005a0001c0001t0005g0210a0001c0001t0005g0211others(21): Show | 24 | HG01081.hp2 HG01106.hp2 HG01109.hp1 others(21): Show |
intron_variant | MODIFIER | c.199-4186A>G | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 1/17 | chr15 | 41434135 | ||||||
| chr15:41434144
|
C | CT | 18 | a0001c0001t0001g0013a0001c0001t0001g0138a0001c0001t0002g0114others(15): Show | 18 | HG01081.hp2 HG01106.hp2 HG01257.hp1 others(15): Show |
intron_variant | MODIFIER | c.199-4159dupT | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr15 | 41434144 | |||||
| chr15:41434144
|
CT | C | 45 | a0001c0001t0001g0005a0001c0001t0001g0062a0001c0001t0001g0095others(42): Show | 45 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(42): Show |
intron_variant | MODIFIER | c.199-4159delT | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr15 | 41434144 | |||||
| chr15:41434144
|
CTT | C | 31 | a0001c0001t0004g0177a0001c0001t0004g0178a0001c0001t0004g0179others(28): Show | 31 | HG00099.hp1 HG00609.hp1 HG01106.hp1 others(28): Show |
intron_variant | MODIFIER | c.199-4160_199-4159d others(4): Show |
RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr15 | 41434144 | |||||
| chr15:41434262
|
C | T | 1 | a0001c0001t0014g0209 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.199-4059C>T | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 1/17 | chr15 | 41434262 | ||||||
| chr15:41434620
|
A | C | 6 | a0001c0001t0001g0005a0001c0001t0009g0004a0001c0001t0009g0006others(3): Show | 6 | HG01109.hp1 HG01243.hp1 HG02145.hp2 others(3): Show |
intron_variant | MODIFIER | c.199-3701A>C | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 1/17 | chr15 | 41434620 | ||||||
| chr15:41434624
|
CT | C | 27 | a0001c0001t0001g0040a0001c0001t0001g0085a0001c0001t0003g0017others(24): Show | 27 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(24): Show |
intron_variant | MODIFIER | c.199-3682delT | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr15 | 41434624 | |||||
| chr15:41434662
|
C | A | 1 | a0001c0001t0004g0178 | 1 | NA18961.hp2 | intron_variant | MODIFIER | c.199-3659C>A | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 1/17 | chr15 | 41434662 | ||||||
| chr15:41434849
|
G | A | 1 | a0001c0001t0011g0200 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.199-3472G>A | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 1/17 | chr15 | 41434849 | ||||||
| chr15:41434874
|
G | A | 1 | a0001c0001t0003g0022 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.199-3447G>A | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 1/17 | chr15 | 41434874 | ||||||
| chr15:41434918
|
C | T | 1 | a0001c0001t0003g0158 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.199-3403C>T | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 1/17 | chr15 | 41434918 | ||||||
| chr15:41434962
|
C | CT | 5 | a0001c0001t0003g0169a0001c0001t0003g0172a0001c0001t0003g0175others(2): Show | 5 | HG02027.hp1 HG02809.hp2 HG02965.hp2 others(2): Show |
intron_variant | MODIFIER | c.199-3343dupT | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr15 | 41434962 | |||||
| chr15:41434962
|
CT | C | 34 | a0001c0001t0003g0002a0001c0001t0003g0017a0001c0001t0003g0018others(31): Show | 34 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(31): Show |
intron_variant | MODIFIER | c.199-3343delT | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr15 | 41434962 | |||||
| chr15:41435000
|
G | A | 1 | a0001c0001t0001g0076 | 1 | HG03492.hp1 | intron_variant | MODIFIER | c.199-3321G>A | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 1/17 | chr15 | 41435000 | ||||||
| chr15:41435201
|
G | T | 1 | a0001c0001t0006g0112 | 1 | NA18980.hp1 | intron_variant | MODIFIER | c.199-3120G>T | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 1/17 | chr15 | 41435201 | ||||||
| chr15:41435378
|
G | T | 1 | a0001c0001t0003g0166 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.199-2943G>T | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 1/17 | chr15 | 41435378 | ||||||
| chr15:41435416
|
C | G | 3 | a0001c0001t0011g0023a0001c0001t0014g0199a0001c0001t0014g0209 | 3 | HG02572.hp2 HG02615.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.199-2905C>G | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 1/17 | chr15 | 41435416 | ||||||
| chr15:41435458
|
G | A | 24 | a0001c0001t0001g0005a0001c0001t0005g0210a0001c0001t0005g0211others(21): Show | 24 | HG01081.hp2 HG01106.hp2 HG01109.hp1 others(21): Show |
intron_variant | MODIFIER | c.199-2863G>A | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 1/17 | chr15 | 41435458 | ||||||
| chr15:41435764
|
T | C | 3 | a0001c0001t0011g0200a0001c0001t0011g0201a0001c0001t0011g0202 | 3 | HG01496.hp1 HG02451.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.199-2557T>C | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 1/17 | chr15 | 41435764 | ||||||
| chr15:41435908
|
CAGTT | C | 2 | a0001c0001t0003g0172a0001c0001t0003g0175 | 2 | HG02965.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.199-2410_199-2407d others(6): Show |
RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr15 | 41435908 | |||||
| chr15:41436060
|
A | T | 15 | a0001c0001t0005g0210a0001c0001t0005g0211a0001c0001t0005g0212others(12): Show | 15 | HG01081.hp2 HG01106.hp2 HG01257.hp1 others(12): Show |
intron_variant | MODIFIER | c.199-2261A>T | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 1/17 | chr15 | 41436060 | ||||||
| chr15:41436078
|
G | A | 34 | a0001c0001t0001g0063a0001c0001t0003g0002a0001c0001t0003g0017others(31): Show | 34 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(31): Show |
intron_variant | MODIFIER | c.199-2243G>A | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 1/17 | chr15 | 41436078 | ||||||
| chr15:41436287
|
T | TA | 20 | a0001c0001t0001g0011a0001c0001t0001g0030a0001c0001t0001g0044others(17): Show | 20 | HG00639.hp2 HG00738.hp1 HG00741.hp1 others(17): Show |
intron_variant | MODIFIER | c.199-2011dupA | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr15 | 41436287 | |||||
| chr15:41436287
|
TA | T | 45 | a0001c0001t0001g0080a0001c0001t0001g0091a0001c0001t0002g0119others(42): Show | 45 | HG00099.hp1 HG00609.hp1 HG01081.hp2 others(42): Show |
intron_variant | MODIFIER | c.199-2011delA | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr15 | 41436287 | |||||
| chr15:41436456
|
C | CA | 15 | a0001c0001t0001g0005a0001c0001t0001g0011a0001c0001t0002g0016others(12): Show | 15 | HG00609.hp2 HG01109.hp1 HG01243.hp1 others(12): Show |
intron_variant | MODIFIER | c.199-1846dupA | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr15 | 41436456 | |||||
| chr15:41436457
|
A | C | 1 | a0001c0001t0007g0025 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.199-1864A>C | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 1/17 | chr15 | 41436457 | ||||||
| chr15:41436623
|
C | CA | 14 | a0001c0001t0001g0056a0001c0001t0002g0127a0001c0001t0002g0133others(11): Show | 14 | HG00544.hp2 HG00558.hp2 HG01109.hp1 others(11): Show |
intron_variant | MODIFIER | c.199-1677dupA | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr15 | 41436623 | |||||
| chr15:41436623
|
CA | C | 7 | a0001c0001t0002g0015a0001c0001t0002g0113a0001c0001t0003g0017others(4): Show | 7 | HG01496.hp1 HG01975.hp1 HG01975.hp2 others(4): Show |
intron_variant | MODIFIER | c.199-1677delA | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr15 | 41436623 | |||||
| chr15:41436667
|
T | C | 1 | a0001c0001t0003g0161 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.199-1654T>C | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 1/17 | chr15 | 41436667 | ||||||
| chr15:41436783
|
GTC | G | 2 | a0001c0001t0001g0011a0001c0001t0002g0016 | 2 | HG04115.hp1 HG04115.hp2 |
intron_variant | MODIFIER | c.199-1534_199-1533d others(4): Show |
RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr15 | 41436783 | |||||
| chr15:41437001
|
C | T | 4 | a0001c0001t0001g0012a0001c0001t0001g0088a0001c0001t0001g0089others(1): Show | 4 | HG00741.hp1 HG03654.hp2 HG03927.hp1 others(1): Show |
intron_variant | MODIFIER | c.199-1320C>T | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 1/17 | chr15 | 41437001 | ||||||
| chr15:41437036
|
G | A | 35 | a0001c0001t0003g0002a0001c0001t0003g0017a0001c0001t0003g0018others(32): Show | 35 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(32): Show |
intron_variant | MODIFIER | c.199-1285G>A | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 1/17 | chr15 | 41437036 | ||||||
| chr15:41437125
|
AT | A | 15 | a0001c0001t0005g0210a0001c0001t0005g0211a0001c0001t0005g0212others(12): Show | 15 | HG01081.hp2 HG01106.hp2 HG01257.hp1 others(12): Show |
intron_variant | MODIFIER | c.199-1195delT | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 1/17 | chr15 | 41437125 | ||||||
| chr15:41437278
|
G | A | 2 | a0001c0001t0001g0040a0001c0001t0001g0063 | 2 | HG02004.hp1 NA18999.hp1 |
intron_variant | MODIFIER | c.199-1043G>A | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 1/17 | chr15 | 41437278 | ||||||
| chr15:41437373
|
C | T | 1 | a0001c0001t0014g0199 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.199-948C>T | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 1/17 | chr15 | 41437373 | ||||||
| chr15:41437528
|
C | A | 1 | a0001c0001t0001g0093 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.199-793C>A | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 1/17 | chr15 | 41437528 | ||||||
| chr15:41437633
|
C | T | 2 | a0001c0001t0001g0026a0001c0001t0007g0087 | 2 | NA18946.hp1 NA19083.hp2 |
intron_variant | MODIFIER | c.199-688C>T | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 1/17 | chr15 | 41437633 | ||||||
| chr15:41437640
|
G | A | 2 | a0001c0001t0007g0208a0001c0001t0022g0081 | 2 | HG00544.hp1 NA19085.hp2 |
intron_variant | MODIFIER | c.199-681G>A | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 1/17 | chr15 | 41437640 | ||||||
| chr15:41437813
|
G | A | 2 | a0001c0001t0004g0182a0001c0001t0004g0188 | 2 | HG01106.hp1 HG02486.hp2 |
intron_variant | MODIFIER | c.199-508G>A | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 1/17 | chr15 | 41437813 | ||||||
| chr15:41437860
|
G | A | 5 | a0001c0001t0010g0052a0001c0001t0010g0054a0001c0001t0010g0055others(2): Show | 5 | HG01891.hp2 HG02717.hp1 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.199-461G>A | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 1/17 | chr15 | 41437860 | ||||||
| chr15:41437914
|
C | T | 7 | a0001c0001t0003g0020a0001c0001t0003g0149a0001c0001t0003g0156others(4): Show | 7 | HG00323.hp2 HG00642.hp1 HG00741.hp2 others(4): Show |
intron_variant | MODIFIER | c.199-407C>T | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 1/17 | chr15 | 41437914 | ||||||
| chr15:41437915
|
T | C | 1 | a0001c0001t0001g0053 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.199-406T>C | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 1/17 | chr15 | 41437915 | ||||||
| chr15:41437928
|
C | T | 6 | a0001c0001t0001g0005a0001c0001t0009g0004a0001c0001t0009g0006others(3): Show | 6 | HG01109.hp1 HG01243.hp1 HG02145.hp2 others(3): Show |
intron_variant | MODIFIER | c.199-393C>T | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 1/17 | chr15 | 41437928 | ||||||
| chr15:41438048
|
G | A | 24 | a0001c0001t0001g0005a0001c0001t0005g0210a0001c0001t0005g0211others(21): Show | 24 | HG01081.hp2 HG01106.hp2 HG01109.hp1 others(21): Show |
intron_variant | MODIFIER | c.199-273G>A | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 1/17 | chr15 | 41438048 | ||||||
| chr15:41438050
|
T | A | 6 | a0001c0001t0001g0005a0001c0001t0009g0004a0001c0001t0009g0006others(3): Show | 6 | HG01109.hp1 HG01243.hp1 HG02145.hp2 others(3): Show |
intron_variant | MODIFIER | c.199-271T>A | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 1/17 | chr15 | 41438050 | ||||||
| chr15:41438967
|
C | CT | 14 | a0001c0001t0001g0005a0001c0001t0001g0013a0001c0001t0001g0038others(11): Show | 14 | HG01109.hp1 HG01243.hp1 HG01496.hp1 others(11): Show |
intron_variant | MODIFIER | c.309+551dupT | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr15 | 41438967 | |||||
| chr15:41438967
|
C | CTT | 15 | a0001c0001t0005g0210a0001c0001t0005g0211a0001c0001t0005g0212others(12): Show | 15 | HG01081.hp2 HG01106.hp2 HG01257.hp1 others(12): Show |
intron_variant | MODIFIER | c.309+550_309+551dup others(2): Show |
RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr15 | 41438967 | |||||
| chr15:41439085
|
G | T | 23 | a0001c0001t0003g0017a0001c0001t0003g0018a0001c0001t0003g0019others(20): Show | 23 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(20): Show |
intron_variant | MODIFIER | c.309+654G>T | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 2/17 | chr15 | 41439085 | ||||||
| chr15:41439162
|
G | C | 28 | a0001c0001t0004g0177a0001c0001t0004g0178a0001c0001t0004g0179others(25): Show | 28 | HG00099.hp1 HG00609.hp1 HG01106.hp1 others(25): Show |
intron_variant | MODIFIER | c.309+731G>C | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 2/17 | chr15 | 41439162 | ||||||
| chr15:41439176
|
C | T | 1 | a0001c0001t0004g0179 | 1 | NA18949.hp1 | intron_variant | MODIFIER | c.309+745C>T | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 2/17 | chr15 | 41439176 | ||||||
| chr15:41439224
|
C | T | 3 | a0001c0001t0011g0200a0001c0001t0011g0201a0001c0001t0011g0202 | 3 | HG01496.hp1 HG02451.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.309+793C>T | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 2/17 | chr15 | 41439224 | ||||||
| chr15:41439352
|
G | A | 34 | a0001c0001t0003g0002a0001c0001t0003g0017a0001c0001t0003g0018others(31): Show | 34 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(31): Show |
intron_variant | MODIFIER | c.309+921G>A | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 2/17 | chr15 | 41439352 | ||||||
| chr15:41439410
|
T | A | 1 | a0001c0001t0001g0043 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.309+979T>A | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 2/17 | chr15 | 41439410 | ||||||
| chr15:41439506
|
A | T | 15 | a0001c0001t0005g0210a0001c0001t0005g0211a0001c0001t0005g0212others(12): Show | 15 | HG01081.hp2 HG01106.hp2 HG01257.hp1 others(12): Show |
intron_variant | MODIFIER | c.309+1075A>T | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 2/17 | chr15 | 41439506 | ||||||
| chr15:41439709
|
C | T | 1 | a0001c0001t0003g0161 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.309+1278C>T | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 2/17 | chr15 | 41439709 | ||||||
| chr15:41439729
|
G | A | 3 | a0001c0001t0006g0098a0001c0001t0006g0099a0001c0001t0006g0100 | 3 | HG00639.hp2 HG00738.hp1 HG03654.hp1 |
intron_variant | MODIFIER | c.309+1298G>A | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 2/17 | chr15 | 41439729 | ||||||
| chr15:41439870
|
T | G | 6 | a0001c0001t0001g0005a0001c0001t0009g0004a0001c0001t0009g0006others(3): Show | 6 | HG01109.hp1 HG01243.hp1 HG02145.hp2 others(3): Show |
intron_variant | MODIFIER | c.309+1439T>G | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 2/17 | chr15 | 41439870 | ||||||
| chr15:41439990
|
T | G | 1 | a0001c0001t0001g0046 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.309+1559T>G | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 2/17 | chr15 | 41439990 | ||||||
| chr15:41440053
|
A | AAAAAATG others(6): Show |
6 | a0001c0001t0001g0005a0001c0001t0009g0004a0001c0001t0009g0006others(3): Show | 6 | HG01109.hp1 HG01243.hp1 HG02145.hp2 others(3): Show |
intron_variant | MODIFIER | c.309+1622_309+1623i others(15): Show |
RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 2/17 | chr15 | 41440053 | ||||||
| chr15:41440054
|
T | A | 6 | a0001c0001t0001g0005a0001c0001t0009g0004a0001c0001t0009g0006others(3): Show | 6 | HG01109.hp1 HG01243.hp1 HG02145.hp2 others(3): Show |
intron_variant | MODIFIER | c.309+1623T>A | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 2/17 | chr15 | 41440054 | ||||||
| chr15:41440057
|
G | A | 6 | a0001c0001t0001g0005a0001c0001t0009g0004a0001c0001t0009g0006others(3): Show | 6 | HG01109.hp1 HG01243.hp1 HG02145.hp2 others(3): Show |
intron_variant | MODIFIER | c.309+1626G>A | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 2/17 | chr15 | 41440057 | ||||||
| chr15:41440184
|
C | CT | 3 | a0001c0001t0003g0149a0001c0001t0003g0164a0001c0001t0003g0174 | 3 | HG00323.hp2 HG00642.hp1 HG00642.hp2 |
intron_variant | MODIFIER | c.309+1756dupT | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr15 | 41440184 | |||||
| chr15:41440186
|
TTC | T | 29 | a0001c0001t0004g0177a0001c0001t0004g0178a0001c0001t0004g0179others(26): Show | 29 | HG00099.hp1 HG00609.hp1 HG01106.hp1 others(26): Show |
intron_variant | MODIFIER | c.309+1757_309+1758d others(4): Show |
RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr15 | 41440186 | |||||
| chr15:41440187
|
TC | T | 24 | a0001c0001t0001g0005a0001c0001t0003g0022a0001c0001t0004g0193others(21): Show | 24 | HG01081.hp2 HG01106.hp2 HG01109.hp1 others(21): Show |
intron_variant | MODIFIER | c.309+1757delC | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 2/17 | chr15 | 41440187 | ||||||
| chr15:41440188
|
C | T | 34 | a0001c0001t0003g0002a0001c0001t0003g0017a0001c0001t0003g0018others(31): Show | 34 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(31): Show |
intron_variant | MODIFIER | c.309+1757C>T | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 2/17 | chr15 | 41440188 | ||||||
| chr15:41440217
|
G | A | 2 | a0001c0001t0001g0039a0001c0001t0001g0050 | 2 | HG01074.hp1 HG01361.hp2 |
intron_variant | MODIFIER | c.309+1786G>A | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 2/17 | chr15 | 41440217 | ||||||
| chr15:41440405
|
G | C | 1 | a0001c0001t0010g0054 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.309+1974G>C | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 2/17 | chr15 | 41440405 | ||||||
| chr15:41440468
|
C | T | 1 | a0001c0001t0001g0095 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.309+2037C>T | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 2/17 | chr15 | 41440468 | ||||||
| chr15:41440490
|
C | CT | 12 | a0001c0001t0001g0005a0001c0001t0001g0029a0001c0001t0003g0172others(9): Show | 12 | HG00609.hp2 HG01109.hp1 HG01243.hp1 others(9): Show |
intron_variant | MODIFIER | c.309+2077dupT | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr15 | 41440490 | |||||
| chr15:41440490
|
C | CTTT | 23 | a0001c0001t0004g0177a0001c0001t0004g0178a0001c0001t0004g0181others(20): Show | 23 | HG00099.hp1 HG01106.hp1 HG01928.hp2 others(20): Show |
intron_variant | MODIFIER | c.309+2075_309+2077d others(5): Show |
RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr15 | 41440490 | |||||
| chr15:41440490
|
C | CTTTT | 5 | a0001c0001t0004g0179a0001c0001t0004g0192a0001c0001t0004g0194others(2): Show | 5 | HG00609.hp1 HG01981.hp1 NA18944.hp1 others(2): Show |
intron_variant | MODIFIER | c.309+2074_309+2077d others(6): Show |
RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr15 | 41440490 | |||||
| chr15:41440594
|
A | G | 6 | a0001c0001t0001g0005a0001c0001t0009g0004a0001c0001t0009g0006others(3): Show | 6 | HG01109.hp1 HG01243.hp1 HG02145.hp2 others(3): Show |
intron_variant | MODIFIER | c.309+2163A>G | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 2/17 | chr15 | 41440594 | ||||||
| chr15:41440680
|
G | A | 2 | a0001c0001t0011g0201a0001c0001t0011g0202 | 2 | HG02451.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.309+2249G>A | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 2/17 | chr15 | 41440680 | ||||||
| chr15:41440856
|
T | TG | 7 | a0001c0001t0001g0005a0001c0001t0003g0174a0001c0001t0009g0004others(4): Show | 7 | HG00642.hp2 HG01109.hp1 HG01243.hp1 others(4): Show |
intron_variant | MODIFIER | c.309+2431dupG | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr15 | 41440856 | |||||
| chr15:41440968
|
C | CT | 52 | a0001c0001t0001g0039a0001c0001t0001g0041a0001c0001t0002g0111others(49): Show | 52 | HG00099.hp2 HG00323.hp2 HG00639.hp1 others(49): Show |
intron_variant | MODIFIER | c.309+2558dupT | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr15 | 41440968 | |||||
| chr15:41440968
|
CT | C | 11 | a0001c0001t0001g0026a0001c0001t0001g0033a0001c0001t0001g0038others(8): Show | 11 | HG00558.hp2 HG02004.hp2 HG02273.hp2 others(8): Show |
intron_variant | MODIFIER | c.309+2558delT | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr15 | 41440968 | |||||
| chr15:41441051
|
A | G | 34 | a0001c0001t0003g0002a0001c0001t0003g0017a0001c0001t0003g0018others(31): Show | 34 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(31): Show |
intron_variant | MODIFIER | c.309+2620A>G | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 2/17 | chr15 | 41441051 | ||||||
| chr15:41441130
|
C | A | 1 | a0001c0001t0001g0094 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.309+2699C>A | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 2/17 | chr15 | 41441130 | ||||||
| chr15:41441134
|
G | A | 2 | a0001c0001t0011g0201a0001c0001t0011g0202 | 2 | HG02451.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.309+2703G>A | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 2/17 | chr15 | 41441134 | ||||||
| chr15:41441206
|
T | C | 4 | a0001c0001t0001g0065a0001c0001t0001g0078a0001c0001t0001g0082others(1): Show | 4 | HG00423.hp2 HG02040.hp1 NA19074.hp2 others(1): Show |
intron_variant | MODIFIER | c.309+2775T>C | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 2/17 | chr15 | 41441206 | ||||||
| chr15:41441390
|
C | T | 1 | a0001c0001t0007g0025 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.309+2959C>T | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 2/17 | chr15 | 41441390 | ||||||
| chr15:41441606
|
T | G | 1 | a0001c0001t0002g0136 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.309+3175T>G | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 2/17 | chr15 | 41441606 | ||||||
| chr15:41441743
|
T | A | 1 | a0001c0001t0004g0191 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.309+3312T>A | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 2/17 | chr15 | 41441743 | ||||||
| chr15:41441760
|
C | T | 1 | a0001c0001t0001g0094 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.309+3329C>T | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 2/17 | chr15 | 41441760 | ||||||
| chr15:41442170
|
A | AT | 7 | a0001c0001t0001g0056a0001c0001t0001g0068a0001c0001t0002g0097others(4): Show | 7 | HG01358.hp2 HG01928.hp1 HG01978.hp1 others(4): Show |
intron_variant | MODIFIER | c.309+3754dupT | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr15 | 41442170 | |||||
| chr15:41442241
|
C | T | 28 | a0001c0001t0004g0177a0001c0001t0004g0178a0001c0001t0004g0179others(25): Show | 28 | HG00099.hp1 HG00609.hp1 HG01106.hp1 others(25): Show |
intron_variant | MODIFIER | c.309+3810C>T | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 2/17 | chr15 | 41442241 | ||||||
| chr15:41442281
|
C | T | 1 | a0001c0001t0016g0150 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.309+3850C>T | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 2/17 | chr15 | 41442281 | ||||||
| chr15:41442343
|
A | G | 1 | a0001c0001t0002g0003 | 1 | HG01517.hp2 | intron_variant | MODIFIER | c.309+3912A>G | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 2/17 | chr15 | 41442343 | ||||||
| chr15:41442484
|
G | A | 1 | a0001c0002t0015g0032 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.309+4053G>A | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 2/17 | chr15 | 41442484 | ||||||
| chr15:41442603
|
G | A | 1 | a0001c0001t0001g0073 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.309+4172G>A | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 2/17 | chr15 | 41442603 | ||||||
| chr15:41442617
|
G | A | 3 | a0001c0001t0011g0200a0001c0001t0011g0201a0001c0001t0011g0202 | 3 | HG01496.hp1 HG02451.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.309+4186G>A | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 2/17 | chr15 | 41442617 | ||||||
| chr15:41442673
|
G | A | 1 | a0001c0005t0007g0083 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.309+4242G>A | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 2/17 | chr15 | 41442673 | ||||||
| chr15:41442692
|
A | G | 1 | a0001c0001t0006g0131 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.309+4261A>G | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 2/17 | chr15 | 41442692 | ||||||
| chr15:41442747
|
G | A | 1 | a0001c0001t0003g0170 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.309+4316G>A | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 2/17 | chr15 | 41442747 | ||||||
| chr15:41442857
|
G | A | 2 | a0001c0001t0009g0004a0001c0001t0009g0007 | 2 | HG01243.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.309+4426G>A | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 2/17 | chr15 | 41442857 | ||||||
| chr15:41443245
|
A | G | 2 | a0001c0001t0001g0059a0001c0001t0001g0064 | 2 | HG03669.hp2 NA20905.hp1 |
intron_variant | MODIFIER | c.309+4814A>G | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 2/17 | chr15 | 41443245 | ||||||
| chr15:41443363
|
A | C | 2 | a0001c0001t0001g0092a0001c0001t0001g0096 | 2 | HG01884.hp1 HG02055.hp1 |
intron_variant | MODIFIER | c.309+4932A>C | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 2/17 | chr15 | 41443363 | ||||||
| chr15:41443510
|
C | A | 90 | a0001c0001t0001g0005a0001c0001t0001g0071a0001c0001t0003g0002others(87): Show | 90 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(87): Show |
intron_variant | MODIFIER | c.309+5079C>A | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 2/17 | chr15 | 41443510 | ||||||
| chr15:41443512
|
T | G | 90 | a0001c0001t0001g0005a0001c0001t0001g0071a0001c0001t0003g0002others(87): Show | 90 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(87): Show |
intron_variant | MODIFIER | c.309+5081T>G | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 2/17 | chr15 | 41443512 | ||||||
| chr15:41443587
|
A | G | 23 | a0001c0001t0003g0017a0001c0001t0003g0018a0001c0001t0003g0019others(20): Show | 23 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(20): Show |
intron_variant | MODIFIER | c.309+5156A>G | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 2/17 | chr15 | 41443587 | ||||||
| chr15:41443597
|
G | A | 3 | a0001c0001t0011g0200a0001c0001t0011g0201a0001c0001t0011g0202 | 3 | HG01496.hp1 HG02451.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.309+5166G>A | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 2/17 | chr15 | 41443597 | ||||||
| chr15:41443602
|
TA | T | 89 | a0001c0001t0001g0005a0001c0001t0001g0071a0001c0001t0003g0002others(86): Show | 89 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(86): Show |
intron_variant | MODIFIER | c.309+5182delA | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr15 | 41443602 | |||||
| chr15:41443784
|
T | C | 3 | a0001c0001t0011g0200a0001c0001t0011g0201a0001c0001t0011g0202 | 3 | HG01496.hp1 HG02451.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.309+5353T>C | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 2/17 | chr15 | 41443784 | ||||||
| chr15:41443846
|
T | C | 1 | a0001c0001t0003g0166 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.309+5415T>C | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 2/17 | chr15 | 41443846 | ||||||
| chr15:41443961
|
T | G | 3 | a0001c0001t0011g0200a0001c0001t0011g0201a0001c0001t0011g0202 | 3 | HG01496.hp1 HG02451.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.309+5530T>G | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 2/17 | chr15 | 41443961 | ||||||
| chr15:41444067
|
C | CA | 7 | a0001c0001t0004g0178a0001c0001t0004g0192a0001c0001t0005g0210others(4): Show | 7 | HG01981.hp1 NA18955.hp2 NA18961.hp2 others(4): Show |
intron_variant | MODIFIER | c.309+5645dupA | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr15 | 41444067 | |||||
| chr15:41444076
|
AC | A | 7 | a0001c0001t0001g0005a0001c0001t0003g0161a0001c0001t0009g0004others(4): Show | 7 | HG00140.hp1 HG01109.hp1 HG01243.hp1 others(4): Show |
intron_variant | MODIFIER | c.309+5646delC | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 2/17 | chr15 | 41444076 | ||||||
| chr15:41444077
|
C | A | 83 | a0001c0001t0001g0071a0001c0001t0003g0002a0001c0001t0003g0017others(80): Show | 83 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(80): Show |
intron_variant | MODIFIER | c.309+5646C>A | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 2/17 | chr15 | 41444077 | ||||||
| chr15:41444092
|
A | G | 1 | a0001c0001t0001g0071 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.309+5661A>G | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 2/17 | chr15 | 41444092 | ||||||
| chr15:41444104
|
T | A | 1 | a0001c0001t0001g0071 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.309+5673T>A | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 2/17 | chr15 | 41444104 | ||||||
| chr15:41444142
|
G | A | 1 | a0001c0001t0011g0023 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.309+5711G>A | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 2/17 | chr15 | 41444142 | ||||||
| chr15:41444243
|
C | G | 1 | a0001c0001t0001g0071 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.309+5812C>G | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 2/17 | chr15 | 41444243 | ||||||
| chr15:41444298
|
A | AT | 6 | a0001c0001t0002g0114a0001c0001t0002g0134a0001c0001t0005g0218others(3): Show | 6 | HG01496.hp1 HG01515.hp2 HG02451.hp2 others(3): Show |
intron_variant | MODIFIER | c.309+5880dupT | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr15 | 41444298 | |||||
| chr15:41444433
|
A | G | 1 | a0001c0001t0001g0091 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.309+6002A>G | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 2/17 | chr15 | 41444433 | ||||||
| chr15:41444448
|
C | T | 1 | a0001c0001t0001g0040 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.309+6017C>T | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 2/17 | chr15 | 41444448 | ||||||
| chr15:41444454
|
C | T | 1 | a0001c0001t0001g0026 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.309+6023C>T | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 2/17 | chr15 | 41444454 | ||||||
| chr15:41444494
|
C | T | 5 | a0001c0001t0010g0052a0001c0001t0010g0054a0001c0001t0010g0055others(2): Show | 5 | HG01891.hp2 HG02717.hp1 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.309+6063C>T | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 2/17 | chr15 | 41444494 | ||||||
| chr15:41444503
|
C | G | 1 | a0001c0001t0007g0034 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.309+6072C>G | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 2/17 | chr15 | 41444503 | ||||||
| chr15:41444781
|
A | G | 1 | a0001c0001t0003g0022 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.309+6350A>G | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 2/17 | chr15 | 41444781 | ||||||
| chr15:41444804
|
A | G | 1 | a0001c0001t0001g0071 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.309+6373A>G | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 2/17 | chr15 | 41444804 | ||||||
| chr15:41444861
|
T | C | 90 | a0001c0001t0001g0005a0001c0001t0001g0071a0001c0001t0003g0002others(87): Show | 90 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(87): Show |
intron_variant | MODIFIER | c.309+6430T>C | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 2/17 | chr15 | 41444861 | ||||||
| chr15:41444864
|
G | A | 1 | a0001c0001t0011g0023 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.309+6433G>A | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 2/17 | chr15 | 41444864 | ||||||
| chr15:41444942
|
A | T | 1 | a0001c0001t0007g0075 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.309+6511A>T | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 2/17 | chr15 | 41444942 | ||||||
| chr15:41445077
|
G | A | 1 | a0001c0001t0009g0084 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.309+6646G>A | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 2/17 | chr15 | 41445077 | ||||||
| chr15:41445081
|
A | G | 1 | a0001c0001t0003g0002 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.309+6650A>G | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 2/17 | chr15 | 41445081 | ||||||
| chr15:41445171
|
G | A | 6 | a0001c0001t0001g0005a0001c0001t0009g0004a0001c0001t0009g0006others(3): Show | 6 | HG01109.hp1 HG01243.hp1 HG02145.hp2 others(3): Show |
intron_variant | MODIFIER | c.309+6740G>A | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 2/17 | chr15 | 41445171 | ||||||
| chr15:41445449
|
G | A | 1 | a0001c0001t0005g0214 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.309+7018G>A | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 2/17 | chr15 | 41445449 | ||||||
| chr15:41445583
|
T | G | 15 | a0001c0001t0005g0210a0001c0001t0005g0211a0001c0001t0005g0212others(12): Show | 15 | HG01081.hp2 HG01106.hp2 HG01257.hp1 others(12): Show |
intron_variant | MODIFIER | c.309+7152T>G | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 2/17 | chr15 | 41445583 | ||||||
| chr15:41445636
|
C | G | 1 | a0001c0001t0001g0071 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.309+7205C>G | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 2/17 | chr15 | 41445636 | ||||||
| chr15:41445734
|
A | AT | 7 | a0001c0001t0001g0031a0001c0001t0001g0071a0001c0001t0004g0178others(4): Show | 7 | HG01496.hp1 HG02027.hp2 HG02451.hp1 others(4): Show |
intron_variant | MODIFIER | c.310-7149dupT | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr15 | 41445734 | |||||
| chr15:41445759
|
A | C | 1 | a0001c0001t0001g0077 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.310-7142A>C | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 2/17 | chr15 | 41445759 | ||||||
| chr15:41445964
|
C | A | 1 | a0001c0001t0001g0071 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.310-6937C>A | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 2/17 | chr15 | 41445964 | ||||||
| chr15:41446090
|
C | T | 1 | a0001c0001t0014g0199 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.310-6811C>T | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 2/17 | chr15 | 41446090 | ||||||
| chr15:41446318
|
C | T | 2 | a0001c0001t0001g0039a0001c0001t0001g0050 | 2 | HG01074.hp1 HG01361.hp2 |
intron_variant | MODIFIER | c.310-6583C>T | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 2/17 | chr15 | 41446318 | ||||||
| chr15:41446364
|
A | G | 1 | a0001c0001t0001g0048 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.310-6537A>G | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 2/17 | chr15 | 41446364 | ||||||
| chr15:41446439
|
G | A | 34 | a0001c0001t0003g0002a0001c0001t0003g0017a0001c0001t0003g0018others(31): Show | 34 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(31): Show |
intron_variant | MODIFIER | c.310-6462G>A | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 2/17 | chr15 | 41446439 | ||||||
| chr15:41446525
|
C | T | 3 | a0001c0001t0001g0035a0001c0001t0001g0041a0001c0001t0001g0051 | 3 | HG02129.hp2 HG02165.hp1 NA18980.hp2 |
intron_variant | MODIFIER | c.310-6376C>T | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 2/17 | chr15 | 41446525 | ||||||
| chr15:41446568
|
A | G | 1 | a0001c0001t0004g0179 | 1 | NA18949.hp1 | intron_variant | MODIFIER | c.310-6333A>G | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 2/17 | chr15 | 41446568 | ||||||
| chr15:41446569
|
A | ATTACT | 89 | a0001c0001t0001g0005a0001c0001t0001g0071a0001c0001t0003g0002others(86): Show | 89 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(86): Show |
intron_variant | MODIFIER | c.310-6329_310-6328i others(7): Show |
RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr15 | 41446569 | |||||
| chr15:41446645
|
C | A | 1 | a0001c0001t0003g0022 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.310-6256C>A | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 2/17 | chr15 | 41446645 | ||||||
| chr15:41446803
|
A | AT | 8 | a0001c0001t0001g0012a0001c0001t0001g0092a0001c0001t0001g0095others(5): Show | 8 | HG01106.hp2 HG01884.hp1 HG02055.hp1 others(5): Show |
intron_variant | MODIFIER | c.310-6081dupT | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr15 | 41446803 | |||||
| chr15:41446807
|
T | A | 24 | a0001c0001t0001g0046a0001c0001t0003g0017a0001c0001t0003g0018others(21): Show | 24 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(21): Show |
intron_variant | MODIFIER | c.310-6094T>A | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 2/17 | chr15 | 41446807 | ||||||
| chr15:41446811
|
T | A | 1 | a0001c0001t0003g0163 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.310-6090T>A | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 2/17 | chr15 | 41446811 | ||||||
| chr15:41447158
|
T | G | 6 | a0001c0001t0001g0027a0001c0001t0001g0029a0001c0001t0001g0030others(3): Show | 6 | HG02145.hp1 HG02809.hp1 HG03041.hp2 others(3): Show |
intron_variant | MODIFIER | c.310-5743T>G | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 2/17 | chr15 | 41447158 | ||||||
| chr15:41447278
|
T | G | 1 | a0001c0001t0009g0084 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.310-5623T>G | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 2/17 | chr15 | 41447278 | ||||||
| chr15:41447346
|
G | A | 2 | a0001c0001t0001g0013a0001c0001t0007g0075 | 2 | HG03098.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.310-5555G>A | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 2/17 | chr15 | 41447346 | ||||||
| chr15:41447440
|
C | T | 1 | a0001c0006t0008g0144 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.310-5461C>T | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 2/17 | chr15 | 41447440 | ||||||
| chr15:41447774
|
G | A | 4 | a0001c0001t0013g0024a0001c0001t0013g0204a0001c0001t0013g0205others(1): Show | 4 | NA18955.hp2 NA18968.hp2 NA18971.hp2 others(1): Show |
intron_variant | MODIFIER | c.310-5127G>A | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 2/17 | chr15 | 41447774 | ||||||
| chr15:41447811
|
G | A | 1 | a0001c0001t0003g0149 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.310-5090G>A | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 2/17 | chr15 | 41447811 | ||||||
| chr15:41447811
|
G | T | 1 | a0001c0001t0001g0047 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.310-5090G>T | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 2/17 | chr15 | 41447811 | ||||||
| chr15:41448275
|
A | G | 1 | a0001c0001t0003g0170 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.310-4626A>G | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 2/17 | chr15 | 41448275 | ||||||
| chr15:41448281
|
A | G | 6 | a0001c0001t0001g0005a0001c0001t0009g0004a0001c0001t0009g0006others(3): Show | 6 | HG01109.hp1 HG01243.hp1 HG02145.hp2 others(3): Show |
intron_variant | MODIFIER | c.310-4620A>G | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 2/17 | chr15 | 41448281 | ||||||
| chr15:41448366
|
T | A | 1 | a0001c0001t0008g0142 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.310-4535T>A | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 2/17 | chr15 | 41448366 | ||||||
| chr15:41448946
|
G | A | 3 | a0001c0001t0011g0200a0001c0001t0011g0201a0001c0001t0011g0202 | 3 | HG01496.hp1 HG02451.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.310-3955G>A | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 2/17 | chr15 | 41448946 | ||||||
| chr15:41449227
|
A | AT | 16 | a0001c0001t0001g0011a0001c0001t0001g0059a0001c0001t0001g0064others(13): Show | 16 | HG00741.hp1 HG01496.hp1 HG01978.hp1 others(13): Show |
intron_variant | MODIFIER | c.310-3653dupT | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr15 | 41449227 | |||||
| chr15:41449227
|
A | ATT | 31 | a0001c0001t0003g0002a0001c0001t0003g0017a0001c0001t0003g0018others(28): Show | 31 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(28): Show |
intron_variant | MODIFIER | c.310-3654_310-3653d others(4): Show |
RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr15 | 41449227 | |||||
| chr15:41449227
|
A | ATTTTT | 18 | a0001c0001t0004g0177a0001c0001t0004g0178a0001c0001t0004g0179others(15): Show | 18 | HG00609.hp1 HG01106.hp1 HG01975.hp2 others(15): Show |
intron_variant | MODIFIER | c.310-3657_310-3653d others(7): Show |
RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr15 | 41449227 | |||||
| chr15:41449227
|
A | ATTTTTT | 10 | a0001c0001t0004g0182a0001c0001t0004g0184a0001c0001t0004g0192others(7): Show | 10 | HG00099.hp1 HG01928.hp2 HG01981.hp1 others(7): Show |
intron_variant | MODIFIER | c.310-3658_310-3653d others(8): Show |
RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr15 | 41449227 | |||||
| chr15:41449227
|
A | ATTTTTTT others(5): Show |
4 | a0001c0001t0001g0005a0001c0001t0009g0004a0001c0001t0009g0006others(1): Show | 4 | HG01243.hp1 HG02922.hp1 NA18906.hp2 others(1): Show |
intron_variant | MODIFIER | c.310-3664_310-3653d others(14): Show |
RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr15 | 41449227 | |||||
| chr15:41449227
|
A | ATTTTTTT others(6): Show |
2 | a0001c0001t0009g0008a0001c0001t0009g0009 | 2 | HG01109.hp1 HG02145.hp2 |
intron_variant | MODIFIER | c.310-3665_310-3653d others(15): Show |
RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr15 | 41449227 | |||||
| chr15:41449227
|
A | ATTTTTTT others(7): Show |
9 | a0001c0001t0005g0210a0001c0001t0005g0211a0001c0001t0005g0212others(6): Show | 9 | HG01081.hp2 HG01257.hp1 HG01258.hp2 others(6): Show |
intron_variant | MODIFIER | c.310-3666_310-3653d others(16): Show |
RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr15 | 41449227 | |||||
| chr15:41449227
|
A | ATTTTTTT others(8): Show |
3 | a0001c0001t0005g0213a0001c0001t0005g0214a0001c0001t0005g0216 | 3 | HG01106.hp2 HG01891.hp1 HG04199.hp1 |
intron_variant | MODIFIER | c.310-3667_310-3653d others(17): Show |
RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr15 | 41449227 | |||||
| chr15:41449227
|
A | ATTTTTTT others(9): Show |
1 | a0001c0001t0005g0221 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.310-3668_310-3653d others(18): Show |
RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr15 | 41449227 | |||||
| chr15:41449227
|
A | ATTTTTTT others(10): Show |
1 | a0001c0001t0005g0224 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.310-3669_310-3653d others(19): Show |
RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr15 | 41449227 | |||||
| chr15:41449227
|
A | ATTTTTTT others(11): Show |
1 | a0001c0001t0005g0223 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.310-3670_310-3653d others(20): Show |
RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr15 | 41449227 | |||||
| chr15:41449284
|
G | A | 34 | a0001c0001t0002g0003a0001c0001t0003g0002a0001c0001t0003g0017others(31): Show | 34 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(31): Show |
intron_variant | MODIFIER | c.310-3617G>A | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 2/17 | chr15 | 41449284 | ||||||
| chr15:41449481
|
C | T | 28 | a0001c0001t0004g0177a0001c0001t0004g0178a0001c0001t0004g0179others(25): Show | 28 | HG00099.hp1 HG00609.hp1 HG01106.hp1 others(25): Show |
intron_variant | MODIFIER | c.310-3420C>T | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 2/17 | chr15 | 41449481 | ||||||
| chr15:41449543
|
A | G | 6 | a0001c0001t0001g0005a0001c0001t0009g0004a0001c0001t0009g0006others(3): Show | 6 | HG01109.hp1 HG01243.hp1 HG02145.hp2 others(3): Show |
intron_variant | MODIFIER | c.310-3358A>G | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 2/17 | chr15 | 41449543 | ||||||
| chr15:41449659
|
T | C | 1 | a0001c0001t0002g0070 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.310-3242T>C | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 2/17 | chr15 | 41449659 | ||||||
| chr15:41449799
|
T | C | 1 | a0001c0001t0006g0100 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.310-3102T>C | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 2/17 | chr15 | 41449799 | ||||||
| chr15:41450013
|
T | A | 1 | a0001c0001t0025g0074 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.310-2888T>A | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 2/17 | chr15 | 41450013 | ||||||
| chr15:41450036
|
A | C | 1 | a0001c0001t0005g0224 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.310-2865A>C | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 2/17 | chr15 | 41450036 | ||||||
| chr15:41450414
|
C | T | 1 | a0001c0001t0001g0073 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.310-2487C>T | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 2/17 | chr15 | 41450414 | ||||||
| chr15:41450445
|
C | T | 28 | a0001c0001t0004g0177a0001c0001t0004g0178a0001c0001t0004g0179others(25): Show | 28 | HG00099.hp1 HG00609.hp1 HG01106.hp1 others(25): Show |
intron_variant | MODIFIER | c.310-2456C>T | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 2/17 | chr15 | 41450445 | ||||||
| chr15:41450454
|
A | G | 1 | a0001c0001t0001g0011 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.310-2447A>G | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 2/17 | chr15 | 41450454 | ||||||
| chr15:41450519
|
A | C | 2 | a0001c0001t0005g0214a0001c0001t0005g0215 | 2 | HG04199.hp1 NA20905.hp2 |
intron_variant | MODIFIER | c.310-2382A>C | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 2/17 | chr15 | 41450519 | ||||||
| chr15:41450564
|
G | A | 1 | a0001c0001t0011g0023 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.310-2337G>A | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 2/17 | chr15 | 41450564 | ||||||
| chr15:41450584
|
C | CA | 7 | a0001c0001t0001g0027a0001c0001t0001g0053a0001c0001t0001g0068others(4): Show | 7 | HG00558.hp1 HG01928.hp1 HG01981.hp2 others(4): Show |
intron_variant | MODIFIER | c.310-2300dupA | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr15 | 41450584 | |||||
| chr15:41450837
|
G | T | 24 | a0001c0001t0001g0005a0001c0001t0005g0210a0001c0001t0005g0211others(21): Show | 24 | HG01081.hp2 HG01106.hp2 HG01109.hp1 others(21): Show |
intron_variant | MODIFIER | c.310-2064G>T | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 2/17 | chr15 | 41450837 | ||||||
| chr15:41451228
|
C | T | 89 | a0001c0001t0001g0005a0001c0001t0003g0002a0001c0001t0003g0017others(86): Show | 89 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(86): Show |
intron_variant | MODIFIER | c.310-1673C>T | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 2/17 | chr15 | 41451228 | ||||||
| chr15:41451244
|
A | T | 1 | a0001c0001t0003g0153 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.310-1657A>T | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 2/17 | chr15 | 41451244 | ||||||
| chr15:41451302
|
T | C | 1 | a0001c0001t0004g0225 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.310-1599T>C | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 2/17 | chr15 | 41451302 | ||||||
| chr15:41451376
|
T | A | 34 | a0001c0001t0003g0002a0001c0001t0003g0017a0001c0001t0003g0018others(31): Show | 34 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(31): Show |
intron_variant | MODIFIER | c.310-1525T>A | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 2/17 | chr15 | 41451376 | ||||||
| chr15:41451408
|
G | A | 3 | a0001c0001t0011g0200a0001c0001t0011g0201a0001c0001t0011g0202 | 3 | HG01496.hp1 HG02451.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.310-1493G>A | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 2/17 | chr15 | 41451408 | ||||||
| chr15:41451499
|
A | G | 1 | a0001c0001t0011g0200 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.310-1402A>G | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 2/17 | chr15 | 41451499 | ||||||
| chr15:41451630
|
T | A | 89 | a0001c0001t0001g0005a0001c0001t0003g0002a0001c0001t0003g0017others(86): Show | 89 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(86): Show |
intron_variant | MODIFIER | c.310-1271T>A | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 2/17 | chr15 | 41451630 | ||||||
| chr15:41451760
|
C | A | 1 | a0001c0001t0004g0179 | 1 | NA18949.hp1 | intron_variant | MODIFIER | c.310-1141C>A | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 2/17 | chr15 | 41451760 | ||||||
| chr15:41451964
|
C | T | 1 | a0001c0001t0003g0156 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.310-937C>T | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 2/17 | chr15 | 41451964 | ||||||
| chr15:41452136
|
T | C | 1 | a0001c0001t0018g0207 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.310-765T>C | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 2/17 | chr15 | 41452136 | ||||||
| chr15:41452270
|
T | C | 3 | a0001c0001t0011g0023a0001c0001t0014g0199a0001c0001t0014g0209 | 3 | HG02572.hp2 HG02615.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.310-631T>C | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 2/17 | chr15 | 41452270 | ||||||
| chr15:41452321
|
A | G | 1 | a0001c0001t0030g0180 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.310-580A>G | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 2/17 | chr15 | 41452321 | ||||||
| chr15:41452410
|
C | T | 31 | a0001c0001t0004g0177a0001c0001t0004g0178a0001c0001t0004g0179others(28): Show | 31 | HG00099.hp1 HG00609.hp1 HG01106.hp1 others(28): Show |
intron_variant | MODIFIER | c.310-491C>T | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 2/17 | chr15 | 41452410 | ||||||
| chr15:41452517
|
T | A | 2 | a0001c0001t0001g0106a0001c0001t0002g0049 | 2 | NA19089.hp1 NA19089.hp2 |
intron_variant | MODIFIER | c.310-384T>A | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 2/17 | chr15 | 41452517 | ||||||
| chr15:41452891
|
C | T | 1 | a0001c0001t0001g0117 | 1 | NA19074.hp1 | intron_variant | MODIFIER | c.310-10C>T | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 2/17 | chr15 | 41452891 | ||||||
| chr15:41453130
|
G | C | 3 | a0001c0001t0006g0103a0001c0001t0006g0112a0001c0001t0006g0118 | 3 | HG00544.hp2 NA18961.hp1 NA18980.hp1 |
intron_variant | MODIFIER | c.457+82G>C | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 3/17 | chr15 | 41453130 | ||||||
| chr15:41453499
|
G | A | 1 | a0001c0001t0014g0199 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.457+451G>A | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 3/17 | chr15 | 41453499 | ||||||
| chr15:41453632
|
C | T | 3 | a0001c0001t0011g0200a0001c0001t0011g0201a0001c0001t0011g0202 | 3 | HG01496.hp1 HG02451.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.457+584C>T | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 3/17 | chr15 | 41453632 | ||||||
| chr15:41453993
|
A | G | 3 | a0001c0001t0012g0021a0001c0001t0012g0168a0001c0001t0012g0171 | 3 | HG02055.hp2 HG03130.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.457+945A>G | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 3/17 | chr15 | 41453993 | ||||||
| chr15:41454078
|
G | A | 34 | a0001c0001t0003g0002a0001c0001t0003g0017a0001c0001t0003g0018others(31): Show | 34 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(31): Show |
intron_variant | MODIFIER | c.457+1030G>A | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 3/17 | chr15 | 41454078 | ||||||
| chr15:41454126
|
C | T | 1 | a0001c0001t0004g0178 | 1 | NA18961.hp2 | intron_variant | MODIFIER | c.457+1078C>T | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 3/17 | chr15 | 41454126 | ||||||
| chr15:41454127
|
G | A | 1 | a0001c0001t0001g0043 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.457+1079G>A | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 3/17 | chr15 | 41454127 | ||||||
| chr15:41454170
|
C | T | 1 | a0001c0001t0001g0064 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.457+1122C>T | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 3/17 | chr15 | 41454170 | ||||||
| chr15:41454281
|
G | A | 15 | a0001c0001t0005g0210a0001c0001t0005g0211a0001c0001t0005g0212others(12): Show | 15 | HG01081.hp2 HG01106.hp2 HG01257.hp1 others(12): Show |
intron_variant | MODIFIER | c.457+1233G>A | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 3/17 | chr15 | 41454281 | ||||||
| chr15:41454337
|
T | C | 90 | a0001c0001t0001g0005a0001c0001t0003g0002a0001c0001t0003g0017others(87): Show | 90 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(87): Show |
intron_variant | MODIFIER | c.457+1289T>C | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 3/17 | chr15 | 41454337 | ||||||
| chr15:41454400
|
T | A | 15 | a0001c0001t0005g0210a0001c0001t0005g0211a0001c0001t0005g0212others(12): Show | 15 | HG01081.hp2 HG01106.hp2 HG01257.hp1 others(12): Show |
intron_variant | MODIFIER | c.457+1352T>A | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 3/17 | chr15 | 41454400 | ||||||
| chr15:41454427
|
A | G | 90 | a0001c0001t0001g0005a0001c0001t0003g0002a0001c0001t0003g0017others(87): Show | 90 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(87): Show |
intron_variant | MODIFIER | c.457+1379A>G | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 3/17 | chr15 | 41454427 | ||||||
| chr15:41454812
|
T | C | 1 | a0001c0001t0005g0224 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.457+1764T>C | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 3/17 | chr15 | 41454812 | ||||||
| chr15:41454863
|
T | C | 1 | a0001c0001t0002g0127 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.457+1815T>C | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 3/17 | chr15 | 41454863 | ||||||
| chr15:41454890
|
A | G | 1 | a0001c0001t0002g0126 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.457+1842A>G | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 3/17 | chr15 | 41454890 | ||||||
| chr15:41455069
|
A | G | 1 | a0001c0001t0003g0159 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.457+2021A>G | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 3/17 | chr15 | 41455069 | ||||||
| chr15:41455185
|
C | A | 24 | a0001c0001t0001g0005a0001c0001t0005g0210a0001c0001t0005g0211others(21): Show | 24 | HG01081.hp2 HG01106.hp2 HG01109.hp1 others(21): Show |
intron_variant | MODIFIER | c.457+2137C>A | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 3/17 | chr15 | 41455185 | ||||||
| chr15:41455400
|
G | A | 90 | a0001c0001t0001g0005a0001c0001t0003g0002a0001c0001t0003g0017others(87): Show | 90 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(87): Show |
intron_variant | MODIFIER | c.458-2272G>A | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 3/17 | chr15 | 41455400 | ||||||
| chr15:41455443
|
G | A | 3 | a0001c0001t0011g0023a0001c0001t0014g0199a0001c0001t0014g0209 | 3 | HG02572.hp2 HG02615.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.458-2229G>A | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 3/17 | chr15 | 41455443 | ||||||
| chr15:41455458
|
G | GT | 4 | a0001c0001t0013g0024a0001c0001t0013g0204a0001c0001t0013g0205others(1): Show | 4 | NA18955.hp2 NA18968.hp2 NA18971.hp2 others(1): Show |
intron_variant | MODIFIER | c.458-2213dupT | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr15 | 41455458 | |||||
| chr15:41455498
|
G | A | 5 | a0001c0001t0002g0015a0001c0001t0002g0145a0001c0001t0008g0104others(2): Show | 5 | NA18962.hp2 NA18971.hp1 NA18999.hp2 others(2): Show |
intron_variant | MODIFIER | c.458-2174G>A | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 3/17 | chr15 | 41455498 | ||||||
| chr15:41455603
|
G | C | 1 | a0001c0001t0001g0046 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.458-2069G>C | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 3/17 | chr15 | 41455603 | ||||||
| chr15:41455675
|
C | T | 1 | a0001c0001t0003g0022 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.458-1997C>T | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 3/17 | chr15 | 41455675 | ||||||
| chr15:41455745
|
C | T | 3 | a0001c0001t0011g0023a0001c0001t0014g0199a0001c0001t0014g0209 | 3 | HG02572.hp2 HG02615.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.458-1927C>T | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 3/17 | chr15 | 41455745 | ||||||
| chr15:41455847
|
A | G | 1 | a0001c0001t0004g0185 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.458-1825A>G | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 3/17 | chr15 | 41455847 | ||||||
| chr15:41456130
|
C | G | 3 | a0001c0001t0003g0169a0001c0001t0003g0172a0001c0001t0003g0175 | 3 | HG02809.hp2 HG02965.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.458-1542C>G | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 3/17 | chr15 | 41456130 | ||||||
| chr15:41456190
|
C | CA | 37 | a0001c0001t0001g0005a0001c0001t0001g0044a0001c0001t0003g0153others(34): Show | 37 | HG00099.hp1 HG00609.hp1 HG00738.hp1 others(34): Show |
intron_variant | MODIFIER | c.458-1468dupA | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr15 | 41456190 | |||||
| chr15:41456330
|
T | A | 6 | a0001c0001t0001g0005a0001c0001t0009g0004a0001c0001t0009g0006others(3): Show | 6 | HG01109.hp1 HG01243.hp1 HG02145.hp2 others(3): Show |
intron_variant | MODIFIER | c.458-1342T>A | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 3/17 | chr15 | 41456330 | ||||||
| chr15:41456350
|
G | A | 2 | a0001c0001t0001g0092a0001c0001t0001g0096 | 2 | HG01884.hp1 HG02055.hp1 |
intron_variant | MODIFIER | c.458-1322G>A | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 3/17 | chr15 | 41456350 | ||||||
| chr15:41456414
|
G | A | 47 | a0001c0001t0001g0001a0001c0001t0001g0012a0001c0001t0001g0035others(44): Show | 48 | HG00423.hp2 HG00544.hp1 HG00558.hp1 others(45): Show |
intron_variant | MODIFIER | c.458-1258G>A | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 3/17 | chr15 | 41456414 | ||||||
| chr15:41456488
|
C | CA | 50 | a0001c0001t0001g0040a0001c0001t0001g0063a0001c0001t0003g0002others(47): Show | 50 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(47): Show |
intron_variant | MODIFIER | c.458-1169dupA | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr15 | 41456488 | |||||
| chr15:41456586
|
C | T | 3 | a0001c0001t0011g0023a0001c0001t0014g0199a0001c0001t0014g0209 | 3 | HG02572.hp2 HG02615.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.458-1086C>T | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 3/17 | chr15 | 41456586 | ||||||
| chr15:41456635
|
G | A | 24 | a0001c0001t0001g0005a0001c0001t0005g0210a0001c0001t0005g0211others(21): Show | 24 | HG01081.hp2 HG01106.hp2 HG01109.hp1 others(21): Show |
intron_variant | MODIFIER | c.458-1037G>A | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 3/17 | chr15 | 41456635 | ||||||
| chr15:41456713
|
C | T | 1 | a0001c0001t0007g0025 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.458-959C>T | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 3/17 | chr15 | 41456713 | ||||||
| chr15:41456950
|
G | C | 29 | a0001c0001t0004g0177a0001c0001t0004g0178a0001c0001t0004g0179others(26): Show | 29 | HG00099.hp1 HG00609.hp1 HG01106.hp1 others(26): Show |
intron_variant | MODIFIER | c.458-722G>C | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 3/17 | chr15 | 41456950 | ||||||
| chr15:41456952
|
C | T | 1 | a0001c0001t0009g0006 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.458-720C>T | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 3/17 | chr15 | 41456952 | ||||||
| chr15:41457012
|
G | A | 6 | a0001c0001t0001g0005a0001c0001t0009g0004a0001c0001t0009g0006others(3): Show | 6 | HG01109.hp1 HG01243.hp1 HG02145.hp2 others(3): Show |
intron_variant | MODIFIER | c.458-660G>A | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 3/17 | chr15 | 41457012 | ||||||
| chr15:41457136
|
G | A | 3 | a0001c0001t0011g0200a0001c0001t0011g0201a0001c0001t0011g0202 | 3 | HG01496.hp1 HG02451.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.458-536G>A | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 3/17 | chr15 | 41457136 | ||||||
| chr15:41457174
|
G | A | 6 | a0001c0001t0001g0005a0001c0001t0009g0004a0001c0001t0009g0006others(3): Show | 6 | HG01109.hp1 HG01243.hp1 HG02145.hp2 others(3): Show |
intron_variant | MODIFIER | c.458-498G>A | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 3/17 | chr15 | 41457174 | ||||||
| chr15:41457193
|
A | G | 5 | a0001c0001t0002g0003a0001c0001t0002g0109a0001c0001t0002g0127others(2): Show | 5 | HG00280.hp2 HG00323.hp1 HG00738.hp2 others(2): Show |
intron_variant | MODIFIER | c.458-479A>G | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 3/17 | chr15 | 41457193 | ||||||
| chr15:41457232
|
A | G | 1 | a0001c0001t0001g0011 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.458-440A>G | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 3/17 | chr15 | 41457232 | ||||||
| chr15:41457294
|
G | C | 15 | a0001c0001t0005g0210a0001c0001t0005g0211a0001c0001t0005g0212others(12): Show | 15 | HG01081.hp2 HG01106.hp2 HG01257.hp1 others(12): Show |
intron_variant | MODIFIER | c.458-378G>C | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 3/17 | chr15 | 41457294 | ||||||
| chr15:41457295
|
AG | A | 15 | a0001c0001t0005g0210a0001c0001t0005g0211a0001c0001t0005g0212others(12): Show | 15 | HG01081.hp2 HG01106.hp2 HG01257.hp1 others(12): Show |
intron_variant | MODIFIER | c.458-375delG | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr15 | 41457295 | |||||
| chr15:41457387
|
G | T | 15 | a0001c0001t0005g0210a0001c0001t0005g0211a0001c0001t0005g0212others(12): Show | 15 | HG01081.hp2 HG01106.hp2 HG01257.hp1 others(12): Show |
intron_variant | MODIFIER | c.458-285G>T | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 3/17 | chr15 | 41457387 | ||||||
| chr15:41457457
|
C | T | 1 | a0001c0001t0006g0112 | 1 | NA18980.hp1 | intron_variant | MODIFIER | c.458-215C>T | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 3/17 | chr15 | 41457457 | ||||||
| chr15:41457478
|
T | C | 1 | a0001c0001t0003g0153 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.458-194T>C | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 3/17 | chr15 | 41457478 | ||||||
| chr15:41457898
|
T | TC | 12 | a0001c0001t0001g0013a0001c0001t0001g0035a0001c0001t0001g0088others(9): Show | 12 | HG00738.hp1 HG00741.hp1 HG02055.hp2 others(9): Show |
intron_variant | MODIFIER | c.662+31dupC | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 4/17 | INFO_REALIGN_3_PRIME | chr15 | 41457898 | |||||
| chr15:41457898
|
TC | T | 85 | a0001c0001t0001g0005a0001c0001t0001g0011a0001c0001t0001g0027others(82): Show | 85 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(82): Show |
intron_variant | MODIFIER | c.662+31delC | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 4/17 | INFO_REALIGN_3_PRIME | chr15 | 41457898 | |||||
| chr15:41458250
|
C | T | 6 | a0001c0001t0001g0005a0001c0001t0009g0004a0001c0001t0009g0006others(3): Show | 6 | HG01109.hp1 HG01243.hp1 HG02145.hp2 others(3): Show |
intron_variant | MODIFIER | c.662+374C>T | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 4/17 | chr15 | 41458250 | ||||||
| chr15:41458616
|
T | G | 3 | a0001c0001t0011g0200a0001c0001t0011g0201a0001c0001t0011g0202 | 3 | HG01496.hp1 HG02451.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.662+740T>G | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 4/17 | chr15 | 41458616 | ||||||
| chr15:41458750
|
AAAAAAT | A | 3 | a0001c0001t0011g0200a0001c0001t0011g0201a0001c0001t0011g0202 | 3 | HG01496.hp1 HG02451.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.662+890_662+895del others(6): Show |
RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 4/17 | INFO_REALIGN_3_PRIME | chr15 | 41458750 | |||||
| chr15:41459107
|
G | A | 1 | a0001c0001t0003g0151 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.662+1231G>A | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 4/17 | chr15 | 41459107 | ||||||
| chr15:41459160
|
C | G | 1 | a0001c0001t0001g0065 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.662+1284C>G | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 4/17 | chr15 | 41459160 | ||||||
| chr15:41459480
|
C | T | 22 | a0001c0001t0003g0017a0001c0001t0003g0018a0001c0001t0003g0019others(19): Show | 22 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(19): Show |
intron_variant | MODIFIER | c.662+1604C>T | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 4/17 | chr15 | 41459480 | ||||||
| chr15:41459829
|
G | C | 3 | a0001c0001t0011g0023a0001c0001t0014g0199a0001c0001t0014g0209 | 3 | HG02572.hp2 HG02615.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.662+1953G>C | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 4/17 | chr15 | 41459829 | ||||||
| chr15:41459861
|
C | T | 1 | a0001c0001t0001g0011 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.662+1985C>T | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 4/17 | chr15 | 41459861 | ||||||
| chr15:41459957
|
G | A | 15 | a0001c0001t0005g0210a0001c0001t0005g0211a0001c0001t0005g0212others(12): Show | 15 | HG01081.hp2 HG01106.hp2 HG01257.hp1 others(12): Show |
intron_variant | MODIFIER | c.662+2081G>A | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 4/17 | chr15 | 41459957 | ||||||
| chr15:41460052
|
T | G | 1 | a0001c0001t0010g0054 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.662+2176T>G | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 4/17 | chr15 | 41460052 | ||||||
| chr15:41460117
|
TTTTG | T | 34 | a0001c0001t0003g0002a0001c0001t0003g0017a0001c0001t0003g0018others(31): Show | 34 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(31): Show |
intron_variant | MODIFIER | c.662+2245_662+2248d others(6): Show |
RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 4/17 | INFO_REALIGN_3_PRIME | chr15 | 41460117 | |||||
| chr15:41460126
|
T | G | 34 | a0001c0001t0003g0002a0001c0001t0003g0017a0001c0001t0003g0018others(31): Show | 34 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(31): Show |
intron_variant | MODIFIER | c.662+2250T>G | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 4/17 | chr15 | 41460126 | ||||||
| chr15:41460126
|
T | TG | 17 | a0001c0001t0001g0011a0001c0001t0001g0027a0001c0001t0001g0029others(14): Show | 17 | HG00140.hp2 HG02027.hp2 HG02145.hp1 others(14): Show |
intron_variant | MODIFIER | c.662+2250_662+2251i others(3): Show |
RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 4/17 | chr15 | 41460126 | ||||||
| chr15:41460126
|
T | TTG | 26 | a0001c0001t0001g0044a0001c0001t0004g0177a0001c0001t0004g0178others(23): Show | 26 | HG00099.hp1 HG00609.hp1 HG01106.hp1 others(23): Show |
intron_variant | MODIFIER | c.662+2251_662+2252i others(4): Show |
RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 4/17 | INFO_REALIGN_3_PRIME | chr15 | 41460126 | |||||
| chr15:41460127
|
T | TG | 95 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0012others(92): Show | 96 | HG00423.hp2 HG00544.hp1 HG00558.hp1 others(93): Show |
intron_variant | MODIFIER | c.662+2251_662+2252i others(3): Show |
RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 4/17 | chr15 | 41460127 | ||||||
| chr15:41460577
|
C | A | 3 | a0001c0001t0011g0200a0001c0001t0011g0201a0001c0001t0011g0202 | 3 | HG01496.hp1 HG02451.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.662+2701C>A | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 4/17 | chr15 | 41460577 | ||||||
| chr15:41460654
|
C | T | 90 | a0001c0001t0001g0005a0001c0001t0003g0002a0001c0001t0003g0017others(87): Show | 90 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(87): Show |
intron_variant | MODIFIER | c.662+2778C>T | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 4/17 | chr15 | 41460654 | ||||||
| chr15:41460962
|
C | T | 3 | a0001c0001t0012g0021a0001c0001t0012g0168a0001c0001t0012g0171 | 3 | HG02055.hp2 HG03130.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.662+3086C>T | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 4/17 | chr15 | 41460962 | ||||||
| chr15:41461042
|
A | AT | 5 | a0001c0001t0002g0127a0001c0001t0005g0224a0001c0001t0007g0072others(2): Show | 5 | HG01981.hp2 HG02300.hp2 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.662+3183dupT | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 4/17 | INFO_REALIGN_3_PRIME | chr15 | 41461042 | |||||
| chr15:41461354
|
G | A | 3 | a0001c0001t0011g0023a0001c0001t0014g0199a0001c0001t0014g0209 | 3 | HG02572.hp2 HG02615.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.663-3417G>A | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 4/17 | chr15 | 41461354 | ||||||
| chr15:41461527
|
C | T | 1 | a0001c0001t0001g0080 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.663-3244C>T | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 4/17 | chr15 | 41461527 | ||||||
| chr15:41461586
|
G | A | 1 | a0001c0001t0003g0022 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.663-3185G>A | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 4/17 | chr15 | 41461586 | ||||||
| chr15:41461621
|
C | G | 1 | a0001c0001t0003g0018 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.663-3150C>G | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 4/17 | chr15 | 41461621 | ||||||
| chr15:41461704
|
C | T | 1 | a0001c0001t0001g0048 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.663-3067C>T | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 4/17 | chr15 | 41461704 | ||||||
| chr15:41461785
|
G | A | 3 | a0001c0001t0012g0021a0001c0001t0012g0168a0001c0001t0012g0171 | 3 | HG02055.hp2 HG03130.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.663-2986G>A | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 4/17 | chr15 | 41461785 | ||||||
| chr15:41461913
|
T | C | 6 | a0001c0001t0001g0005a0001c0001t0009g0004a0001c0001t0009g0006others(3): Show | 6 | HG01109.hp1 HG01243.hp1 HG02145.hp2 others(3): Show |
intron_variant | MODIFIER | c.663-2858T>C | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 4/17 | chr15 | 41461913 | ||||||
| chr15:41461935
|
T | A | 1 | a0001c0001t0001g0027 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.663-2836T>A | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 4/17 | chr15 | 41461935 | ||||||
| chr15:41461936
|
T | G | 1 | a0001c0001t0001g0027 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.663-2835T>G | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 4/17 | chr15 | 41461936 | ||||||
| chr15:41462268
|
G | C | 1 | a0001c0001t0006g0140 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.663-2503G>C | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 4/17 | chr15 | 41462268 | ||||||
| chr15:41462451
|
C | G | 14 | a0001c0001t0005g0210a0001c0001t0005g0211a0001c0001t0005g0212others(11): Show | 14 | HG01081.hp2 HG01106.hp2 HG01257.hp1 others(11): Show |
intron_variant | MODIFIER | c.663-2320C>G | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 4/17 | chr15 | 41462451 | ||||||
| chr15:41462459
|
C | T | 2 | a0001c0001t0001g0026a0001c0001t0002g0123 | 2 | NA18946.hp1 NA18946.hp2 |
intron_variant | MODIFIER | c.663-2312C>T | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 4/17 | chr15 | 41462459 | ||||||
| chr15:41462581
|
A | G | 1 | a0001c0001t0003g0156 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.663-2190A>G | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 4/17 | chr15 | 41462581 | ||||||
| chr15:41462890
|
G | T | 1 | a0001c0001t0007g0075 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.663-1881G>T | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 4/17 | chr15 | 41462890 | ||||||
| chr15:41462910
|
C | G | 1 | a0001c0001t0001g0096 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.663-1861C>G | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 4/17 | chr15 | 41462910 | ||||||
| chr15:41463349
|
A | T | 1 | a0001c0001t0001g0031 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.663-1422A>T | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 4/17 | chr15 | 41463349 | ||||||
| chr15:41463632
|
C | T | 1 | a0001c0001t0011g0023 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.663-1139C>T | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 4/17 | chr15 | 41463632 | ||||||
| chr15:41463749
|
T | C | 4 | a0001c0001t0013g0024a0001c0001t0013g0204a0001c0001t0013g0205others(1): Show | 4 | NA18955.hp2 NA18968.hp2 NA18971.hp2 others(1): Show |
intron_variant | MODIFIER | c.663-1022T>C | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 4/17 | chr15 | 41463749 | ||||||
| chr15:41463813
|
G | A | 1 | a0001c0006t0008g0144 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.663-958G>A | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 4/17 | chr15 | 41463813 | ||||||
| chr15:41463999
|
A | G | 24 | a0001c0001t0001g0005a0001c0001t0005g0210a0001c0001t0005g0211others(21): Show | 24 | HG01081.hp2 HG01106.hp2 HG01109.hp1 others(21): Show |
intron_variant | MODIFIER | c.663-772A>G | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 4/17 | chr15 | 41463999 | ||||||
| chr15:41464167
|
A | G | 2 | a0001c0001t0001g0029a0001c0001t0009g0028 | 2 | HG02809.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.663-604A>G | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 4/17 | chr15 | 41464167 | ||||||
| chr15:41464331
|
A | G | 10 | a0001c0001t0003g0002a0001c0001t0003g0169a0001c0001t0003g0170others(7): Show | 10 | HG00642.hp2 HG02055.hp2 HG02486.hp1 others(7): Show |
intron_variant | MODIFIER | c.663-440A>G | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 4/17 | chr15 | 41464331 | ||||||
| chr15:41464438
|
G | A | 1 | a0001c0001t0005g0215 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.663-333G>A | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 4/17 | chr15 | 41464438 | ||||||
| chr15:41464637
|
G | C | 1 | a0001c0001t0016g0150 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.663-134G>C | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 4/17 | chr15 | 41464637 | ||||||
| chr15:41464714
|
A | G | 29 | a0001c0001t0004g0177a0001c0001t0004g0178a0001c0001t0004g0179others(26): Show | 29 | HG00099.hp1 HG00609.hp1 HG01106.hp1 others(26): Show |
intron_variant | MODIFIER | c.663-57A>G | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 4/17 | chr15 | 41464714 | ||||||
| chr15:41464933
|
A | AGT | 93 | a0001c0001t0001g0005a0001c0001t0001g0012a0001c0001t0001g0027others(90): Show | 93 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(90): Show |
intron_variant | MODIFIER | c.777+81_777+82dupGT | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 5/17 | INFO_REALIGN_3_PRIME | chr15 | 41464933 | |||||
| chr15:41464933
|
A | AGTGT | 19 | a0001c0001t0001g0001a0001c0001t0001g0033a0001c0001t0001g0039others(16): Show | 20 | HG01074.hp1 HG01109.hp2 HG01168.hp1 others(17): Show |
intron_variant | MODIFIER | c.777+79_777+82dupGT others(2): Show |
RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 5/17 | INFO_REALIGN_3_PRIME | chr15 | 41464933 | |||||
| chr15:41464933
|
A | AGTGTGT | 4 | a0001c0001t0001g0071a0001c0001t0001g0096a0001c0001t0005g0223others(1): Show | 4 | HG02055.hp1 HG02451.hp1 HG02976.hp1 others(1): Show |
intron_variant | MODIFIER | c.777+77_777+82dupGT others(4): Show |
RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 5/17 | INFO_REALIGN_3_PRIME | chr15 | 41464933 | |||||
| chr15:41464933
|
A | AGTGTGTG others(1): Show |
12 | a0001c0001t0001g0013a0001c0001t0005g0210a0001c0001t0005g0211others(9): Show | 12 | HG01081.hp2 HG01106.hp2 HG01515.hp2 others(9): Show |
intron_variant | MODIFIER | c.777+75_777+82dupGT others(6): Show |
RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 5/17 | INFO_REALIGN_3_PRIME | chr15 | 41464933 | |||||
| chr15:41464933
|
A | AGTGTGTG others(3): Show |
2 | a0001c0001t0005g0219a0001c0001t0005g0220 | 2 | HG01257.hp1 HG01258.hp2 |
intron_variant | MODIFIER | c.777+73_777+82dupGT others(8): Show |
RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 5/17 | INFO_REALIGN_3_PRIME | chr15 | 41464933 | |||||
| chr15:41464933
|
AGT | A | 33 | a0001c0001t0002g0070a0001c0001t0002g0107a0001c0001t0002g0130others(30): Show | 33 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(30): Show |
intron_variant | MODIFIER | c.777+81_777+82delGT | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 5/17 | INFO_REALIGN_3_PRIME | chr15 | 41464933 | |||||
| chr15:41464933
|
AGTGT | A | 37 | a0001c0001t0001g0080a0001c0001t0003g0020a0001c0001t0003g0022others(34): Show | 37 | HG00099.hp1 HG00609.hp1 HG00741.hp2 others(34): Show |
intron_variant | MODIFIER | c.777+79_777+82delGT others(2): Show |
RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 5/17 | INFO_REALIGN_3_PRIME | chr15 | 41464933 | |||||
| chr15:41465069
|
G | C | 1 | a0001c0001t0003g0002 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.777+184G>C | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 5/17 | chr15 | 41465069 | ||||||
| chr15:41465325
|
C | T | 1 | a0001c0001t0003g0002 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.777+440C>T | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 5/17 | chr15 | 41465325 | ||||||
| chr15:41465389
|
C | T | 1 | a0001c0001t0003g0161 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.777+504C>T | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 5/17 | chr15 | 41465389 | ||||||
| chr15:41465406
|
C | T | 1 | a0001c0001t0002g0136 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.777+521C>T | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 5/17 | chr15 | 41465406 | ||||||
| chr15:41465469
|
T | C | 91 | a0001c0001t0001g0005a0001c0001t0001g0030a0001c0001t0003g0002others(88): Show | 91 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(88): Show |
intron_variant | MODIFIER | c.777+584T>C | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 5/17 | chr15 | 41465469 | ||||||
| chr15:41465641
|
A | T | 1 | a0001c0001t0001g0089 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.778-500A>T | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 5/17 | chr15 | 41465641 | ||||||
| chr15:41465936
|
C | T | 1 | a0001c0001t0003g0164 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.778-205C>T | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 5/17 | chr15 | 41465936 | ||||||
| chr15:41465955
|
A | G | 3 | a0001c0001t0011g0200a0001c0001t0011g0201a0001c0001t0011g0202 | 3 | HG01496.hp1 HG02451.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.778-186A>G | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 5/17 | chr15 | 41465955 | ||||||
| chr15:41466300
|
C | T | 1 | a0001c0001t0003g0151 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.889+48C>T | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 6/17 | chr15 | 41466300 | ||||||
| chr15:41466696
|
C | T | 1 | a0001c0001t0002g0128 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.889+444C>T | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 6/17 | chr15 | 41466696 | ||||||
| chr15:41466804
|
G | A | 29 | a0001c0001t0004g0177a0001c0001t0004g0178a0001c0001t0004g0179others(26): Show | 29 | HG00099.hp1 HG00609.hp1 HG01106.hp1 others(26): Show |
intron_variant | MODIFIER | c.889+552G>A | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 6/17 | chr15 | 41466804 | ||||||
| chr15:41466959
|
G | A | 29 | a0001c0001t0004g0177a0001c0001t0004g0178a0001c0001t0004g0179others(26): Show | 29 | HG00099.hp1 HG00609.hp1 HG01106.hp1 others(26): Show |
intron_variant | MODIFIER | c.889+707G>A | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 6/17 | chr15 | 41466959 | ||||||
| chr15:41466969
|
T | G | 1 | a0001c0001t0014g0209 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.889+717T>G | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 6/17 | chr15 | 41466969 | ||||||
| chr15:41467342
|
G | A | 1 | a0001c0001t0001g0005 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.889+1090G>A | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 6/17 | chr15 | 41467342 | ||||||
| chr15:41467477
|
G | A | 2 | a0001c0001t0001g0066a0001c0001t0001g0138 | 2 | NA18953.hp1 NA18977.hp2 |
intron_variant | MODIFIER | c.889+1225G>A | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 6/17 | chr15 | 41467477 | ||||||
| chr15:41467592
|
G | A | 1 | a0001c0002t0015g0032 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.889+1340G>A | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 6/17 | chr15 | 41467592 | ||||||
| chr15:41467639
|
C | T | 1 | a0001c0001t0001g0077 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.889+1387C>T | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 6/17 | chr15 | 41467639 | ||||||
| chr15:41467891
|
A | G | 3 | a0001c0001t0011g0200a0001c0001t0011g0201a0001c0001t0011g0202 | 3 | HG01496.hp1 HG02451.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.889+1639A>G | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 6/17 | chr15 | 41467891 | ||||||
| chr15:41467919
|
C | G | 3 | a0001c0001t0011g0200a0001c0001t0011g0201a0001c0001t0011g0202 | 3 | HG01496.hp1 HG02451.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.889+1667C>G | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 6/17 | chr15 | 41467919 | ||||||
| chr15:41468030
|
T | C | 1 | a0001c0002t0015g0032 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.889+1778T>C | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 6/17 | chr15 | 41468030 | ||||||
| chr15:41468164
|
C | T | 1 | a0001c0001t0001g0038 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.889+1912C>T | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 6/17 | chr15 | 41468164 | ||||||
| chr15:41468185
|
A | C | 3 | a0001c0001t0011g0200a0001c0001t0011g0201a0001c0001t0011g0202 | 3 | HG01496.hp1 HG02451.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.889+1933A>C | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 6/17 | chr15 | 41468185 | ||||||
| chr15:41468186
|
TAATAACG others(165): Show |
T | 3 | a0001c0001t0011g0200a0001c0001t0011g0201a0001c0001t0011g0202 | 3 | HG01496.hp1 HG02451.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.889+1935_890-1899d others(2): Show |
RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 6/17 | chr15 | 41468186 | ||||||
| chr15:41468202
|
C | T | 2 | a0001c0001t0005g0214a0001c0001t0005g0215 | 2 | HG04199.hp1 NA20905.hp2 |
intron_variant | MODIFIER | c.889+1950C>T | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 6/17 | chr15 | 41468202 | ||||||
| chr15:41468341
|
G | A | 15 | a0001c0001t0005g0210a0001c0001t0005g0211a0001c0001t0005g0212others(12): Show | 15 | HG01081.hp2 HG01106.hp2 HG01257.hp1 others(12): Show |
intron_variant | MODIFIER | c.890-1916G>A | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 6/17 | chr15 | 41468341 | ||||||
| chr15:41468419
|
A | G | 89 | a0001c0001t0001g0005a0001c0001t0003g0002a0001c0001t0003g0017others(86): Show | 89 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(86): Show |
intron_variant | MODIFIER | c.890-1838A>G | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 6/17 | chr15 | 41468419 | ||||||
| chr15:41468469
|
C | T | 1 | a0001c0001t0005g0224 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.890-1788C>T | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 6/17 | chr15 | 41468469 | ||||||
| chr15:41468507
|
A | C | 30 | a0001c0001t0004g0177a0001c0001t0004g0178a0001c0001t0004g0179others(27): Show | 30 | HG00099.hp1 HG00423.hp1 HG00609.hp1 others(27): Show |
intron_variant | MODIFIER | c.890-1750A>C | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 6/17 | chr15 | 41468507 | ||||||
| chr15:41468508
|
G | A | 29 | a0001c0001t0004g0177a0001c0001t0004g0178a0001c0001t0004g0179others(26): Show | 29 | HG00099.hp1 HG00609.hp1 HG01106.hp1 others(26): Show |
intron_variant | MODIFIER | c.890-1749G>A | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 6/17 | chr15 | 41468508 | ||||||
| chr15:41468511
|
G | A | 1 | a0001c0001t0014g0209 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.890-1746G>A | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 6/17 | chr15 | 41468511 | ||||||
| chr15:41468519
|
A | G | 12 | a0001c0001t0004g0177a0001c0001t0004g0179a0001c0001t0004g0181others(9): Show | 12 | HG01928.hp2 HG01975.hp2 HG02004.hp2 others(9): Show |
intron_variant | MODIFIER | c.890-1738A>G | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 6/17 | chr15 | 41468519 | ||||||
| chr15:41468534
|
G | C | 1 | a0001c0001t0001g0059 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.890-1723G>C | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 6/17 | chr15 | 41468534 | ||||||
| chr15:41468538
|
T | C | 15 | a0001c0001t0005g0210a0001c0001t0005g0211a0001c0001t0005g0212others(12): Show | 15 | HG01081.hp2 HG01106.hp2 HG01257.hp1 others(12): Show |
intron_variant | MODIFIER | c.890-1719T>C | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 6/17 | chr15 | 41468538 | ||||||
| chr15:41468592
|
C | G | 23 | a0001c0001t0002g0137a0001c0001t0003g0017a0001c0001t0003g0018others(20): Show | 23 | HG00140.hp1 HG00323.hp2 HG00639.hp1 others(20): Show |
intron_variant | MODIFIER | c.890-1665C>G | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 6/17 | chr15 | 41468592 | ||||||
| chr15:41468592
|
C | T | 1 | a0001c0001t0014g0209 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.890-1665C>T | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 6/17 | chr15 | 41468592 | ||||||
| chr15:41468595
|
G | A | 5 | a0001c0001t0001g0033a0001c0001t0001g0071a0001c0001t0021g0148others(2): Show | 5 | HG02451.hp1 HG02965.hp1 HG02976.hp2 others(2): Show |
intron_variant | MODIFIER | c.890-1662G>A | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 6/17 | chr15 | 41468595 | ||||||
| chr15:41468596
|
T | C | 10 | a0001c0001t0001g0033a0001c0001t0001g0071a0001c0001t0004g0192others(7): Show | 10 | HG01496.hp1 HG01981.hp1 HG02451.hp1 others(7): Show |
intron_variant | MODIFIER | c.890-1661T>C | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 6/17 | chr15 | 41468596 | ||||||
| chr15:41468608
|
C | T | 1 | a0001c0001t0006g0140 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.890-1649C>T | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 6/17 | chr15 | 41468608 | ||||||
| chr15:41468609
|
A | G | 31 | a0001c0001t0003g0002a0001c0001t0003g0017a0001c0001t0003g0018others(28): Show | 31 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(28): Show |
intron_variant | MODIFIER | c.890-1648A>G | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 6/17 | chr15 | 41468609 | ||||||
| chr15:41468904
|
C | G | 1 | a0001c0001t0011g0200 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.890-1353C>G | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 6/17 | chr15 | 41468904 | ||||||
| chr15:41469125
|
C | CCTGA | 24 | a0001c0001t0001g0005a0001c0001t0005g0210a0001c0001t0005g0211others(21): Show | 24 | HG01081.hp2 HG01106.hp2 HG01109.hp1 others(21): Show |
intron_variant | MODIFIER | c.890-1130_890-1129i others(6): Show |
RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 6/17 | INFO_REALIGN_3_PRIME | chr15 | 41469125 | |||||
| chr15:41469134
|
G | T | 90 | a0001c0001t0001g0005a0001c0001t0003g0002a0001c0001t0003g0017others(87): Show | 90 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(87): Show |
intron_variant | MODIFIER | c.890-1123G>T | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 6/17 | chr15 | 41469134 | ||||||
| chr15:41469339
|
T | A | 1 | a0001c0001t0003g0022 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.890-918T>A | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 6/17 | chr15 | 41469339 | ||||||
| chr15:41469604
|
C | T | 1 | a0001c0001t0001g0077 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.890-653C>T | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 6/17 | chr15 | 41469604 | ||||||
| chr15:41469611
|
C | T | 56 | a0001c0001t0001g0005a0001c0001t0004g0177a0001c0001t0004g0178others(53): Show | 56 | HG00099.hp1 HG00609.hp1 HG01081.hp2 others(53): Show |
intron_variant | MODIFIER | c.890-646C>T | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 6/17 | chr15 | 41469611 | ||||||
| chr15:41469725
|
A | G | 1 | a0001c0001t0002g0145 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.890-532A>G | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 6/17 | chr15 | 41469725 | ||||||
| chr15:41469786
|
A | C | 1 | a0001c0001t0001g0048 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.890-471A>C | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 6/17 | chr15 | 41469786 | ||||||
| chr15:41469827
|
A | G | 1 | a0001c0003t0004g0190 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.890-430A>G | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 6/17 | chr15 | 41469827 | ||||||
| chr15:41469931
|
A | G | 3 | a0001c0001t0011g0200a0001c0001t0011g0201a0001c0001t0011g0202 | 3 | HG01496.hp1 HG02451.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.890-326A>G | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 6/17 | chr15 | 41469931 | ||||||
| chr15:41470112
|
C | T | 3 | a0001c0001t0011g0200a0001c0001t0011g0201a0001c0001t0011g0202 | 3 | HG01496.hp1 HG02451.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.890-145C>T | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 6/17 | chr15 | 41470112 | ||||||
| chr15:41470148
|
G | A | 3 | a0001c0001t0011g0023a0001c0001t0014g0199a0001c0001t0014g0209 | 3 | HG02572.hp2 HG02615.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.890-109G>A | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 6/17 | chr15 | 41470148 | ||||||
| chr15:41470433
|
G | A | 6 | a0001c0001t0001g0005a0001c0001t0009g0004a0001c0001t0009g0006others(3): Show | 6 | HG01109.hp1 HG01243.hp1 HG02145.hp2 others(3): Show |
intron_variant | MODIFIER | c.1025+41G>A | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 7/17 | chr15 | 41470433 | ||||||
| chr15:41470650
|
C | CT | 27 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0033others(24): Show | 27 | HG00140.hp2 HG00423.hp1 HG00741.hp1 others(24): Show |
intron_variant | MODIFIER | c.1025+284dupT | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 7/17 | INFO_REALIGN_3_PRIME | chr15 | 41470650 | |||||
| chr15:41470650
|
CT | C | 79 | a0001c0001t0001g0005a0001c0001t0001g0046a0001c0001t0003g0002others(76): Show | 79 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(76): Show |
intron_variant | MODIFIER | c.1025+284delT | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 7/17 | INFO_REALIGN_3_PRIME | chr15 | 41470650 | |||||
| chr15:41470650
|
CTTTTTTT others(7): Show |
C | 1 | a0001c0001t0001g0092 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1025+271_1025+284d others(16): Show |
RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 7/17 | INFO_REALIGN_3_PRIME | chr15 | 41470650 | |||||
| chr15:41470656
|
T | C | 5 | a0001c0001t0001g0005a0001c0001t0009g0004a0001c0001t0009g0007others(2): Show | 5 | HG01109.hp1 HG01243.hp1 HG02145.hp2 others(2): Show |
intron_variant | MODIFIER | c.1025+264T>C | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 7/17 | chr15 | 41470656 | ||||||
| chr15:41470657
|
T | C | 1 | a0001c0001t0009g0006 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.1025+265T>C | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 7/17 | chr15 | 41470657 | ||||||
| chr15:41470681
|
C | T | 29 | a0001c0001t0004g0177a0001c0001t0004g0178a0001c0001t0004g0179others(26): Show | 29 | HG00099.hp1 HG00609.hp1 HG01106.hp1 others(26): Show |
intron_variant | MODIFIER | c.1025+289C>T | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 7/17 | chr15 | 41470681 | ||||||
| chr15:41470720
|
A | G | 24 | a0001c0001t0001g0005a0001c0001t0005g0210a0001c0001t0005g0211others(21): Show | 24 | HG01081.hp2 HG01106.hp2 HG01109.hp1 others(21): Show |
intron_variant | MODIFIER | c.1025+328A>G | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 7/17 | chr15 | 41470720 | ||||||
| chr15:41470880
|
G | A | 4 | a0001c0001t0006g0103a0001c0001t0006g0112a0001c0001t0006g0118others(1): Show | 4 | HG00544.hp2 NA18961.hp1 NA18964.hp1 others(1): Show |
intron_variant | MODIFIER | c.1026-292G>A | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 7/17 | chr15 | 41470880 | ||||||
| chr15:41471366
|
T | C | 3 | a0001c0001t0011g0200a0001c0001t0011g0201a0001c0001t0011g0202 | 3 | HG01496.hp1 HG02451.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.1203+17T>C | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 8/17 | chr15 | 41471366 | ||||||
| chr15:41471590
|
C | T | 1 | a0001c0001t0001g0011 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.1203+241C>T | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 8/17 | chr15 | 41471590 | ||||||
| chr15:41471721
|
C | A | 2 | a0001c0001t0001g0041a0001c0001t0001g0051 | 2 | HG02129.hp2 HG02165.hp1 |
intron_variant | MODIFIER | c.1203+372C>A | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 8/17 | chr15 | 41471721 | ||||||
| chr15:41471721
|
C | T | 29 | a0001c0001t0004g0177a0001c0001t0004g0178a0001c0001t0004g0179others(26): Show | 29 | HG00099.hp1 HG00609.hp1 HG01106.hp1 others(26): Show |
intron_variant | MODIFIER | c.1203+372C>T | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 8/17 | chr15 | 41471721 | ||||||
| chr15:41471898
|
T | C | 4 | a0001c0001t0001g0027a0001c0001t0001g0029a0001c0001t0001g0030others(1): Show | 4 | HG02145.hp1 HG02809.hp1 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.1203+549T>C | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 8/17 | chr15 | 41471898 | ||||||
| chr15:41471981
|
C | T | 4 | a0001c0001t0001g0012a0001c0001t0001g0088a0001c0001t0001g0089others(1): Show | 4 | HG00741.hp1 HG03654.hp2 HG03927.hp1 others(1): Show |
intron_variant | MODIFIER | c.1203+632C>T | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 8/17 | chr15 | 41471981 | ||||||
| chr15:41472011
|
G | A | 1 | a0001c0001t0008g0014 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.1203+662G>A | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 8/17 | chr15 | 41472011 | ||||||
| chr15:41472215
|
T | G | 3 | a0001c0001t0011g0023a0001c0001t0014g0199a0001c0001t0014g0209 | 3 | HG02572.hp2 HG02615.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.1203+866T>G | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 8/17 | chr15 | 41472215 | ||||||
| chr15:41472324
|
A | G | 90 | a0001c0001t0001g0005a0001c0001t0003g0002a0001c0001t0003g0017others(87): Show | 90 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(87): Show |
intron_variant | MODIFIER | c.1203+975A>G | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 8/17 | chr15 | 41472324 | ||||||
| chr15:41472356
|
G | A | 1 | a0001c0001t0014g0209 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.1203+1007G>A | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 8/17 | chr15 | 41472356 | ||||||
| chr15:41472378
|
T | C | 3 | a0001c0001t0021g0148a0001c0001t0023g0146a0001c0001t0027g0147 | 3 | HG02976.hp2 HG03139.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.1203+1029T>C | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 8/17 | chr15 | 41472378 | ||||||
| chr15:41472502
|
C | T | 7 | a0001c0001t0005g0216a0001c0001t0005g0217a0001c0001t0005g0218others(4): Show | 7 | HG01081.hp2 HG01106.hp2 HG01257.hp1 others(4): Show |
intron_variant | MODIFIER | c.1203+1153C>T | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 8/17 | chr15 | 41472502 | ||||||
| chr15:41472503
|
G | A | 1 | a0001c0001t0002g0111 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.1203+1154G>A | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 8/17 | chr15 | 41472503 | ||||||
| chr15:41472675
|
G | A | 1 | a0001c0001t0003g0163 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.1203+1326G>A | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 8/17 | chr15 | 41472675 | ||||||
| chr15:41472705
|
CT | C | 5 | a0001c0001t0003g0164a0001c0001t0013g0024a0001c0001t0013g0204others(2): Show | 5 | HG00323.hp2 NA18955.hp2 NA18968.hp2 others(2): Show |
intron_variant | MODIFIER | c.1203+1371delT | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 8/17 | INFO_REALIGN_3_PRIME | chr15 | 41472705 | |||||
| chr15:41472903
|
G | T | 1 | a0001c0001t0003g0022 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1203+1554G>T | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 8/17 | chr15 | 41472903 | ||||||
| chr15:41472922
|
T | C | 10 | a0001c0001t0003g0002a0001c0001t0003g0169a0001c0001t0003g0170others(7): Show | 10 | HG00642.hp2 HG02055.hp2 HG02486.hp1 others(7): Show |
intron_variant | MODIFIER | c.1203+1573T>C | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 8/17 | chr15 | 41472922 | ||||||
| chr15:41472931
|
A | G | 10 | a0001c0001t0003g0002a0001c0001t0003g0169a0001c0001t0003g0170others(7): Show | 10 | HG00642.hp2 HG02055.hp2 HG02486.hp1 others(7): Show |
intron_variant | MODIFIER | c.1203+1582A>G | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 8/17 | chr15 | 41472931 | ||||||
| chr15:41473038
|
G | T | 1 | a0001c0001t0005g0224 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.1204-1582G>T | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 8/17 | chr15 | 41473038 | ||||||
| chr15:41473072
|
C | T | 6 | a0001c0001t0001g0033a0001c0001t0001g0071a0001c0001t0007g0034others(3): Show | 6 | HG02451.hp1 HG02615.hp2 HG02965.hp1 others(3): Show |
intron_variant | MODIFIER | c.1204-1548C>T | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 8/17 | chr15 | 41473072 | ||||||
| chr15:41473086
|
T | C | 1 | a0001c0001t0003g0002 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.1204-1534T>C | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 8/17 | chr15 | 41473086 | ||||||
| chr15:41473156
|
C | T | 1 | a0001c0001t0001g0069 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.1204-1464C>T | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 8/17 | chr15 | 41473156 | ||||||
| chr15:41473278
|
C | T | 1 | a0001c0001t0007g0072 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.1204-1342C>T | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 8/17 | chr15 | 41473278 | ||||||
| chr15:41473279
|
G | A | 1 | a0001c0001t0004g0191 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.1204-1341G>A | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 8/17 | chr15 | 41473279 | ||||||
| chr15:41473442
|
G | GT | 12 | a0001c0001t0001g0013a0001c0001t0001g0026a0001c0001t0001g0027others(9): Show | 12 | HG00639.hp1 HG00741.hp1 HG02145.hp1 others(9): Show |
intron_variant | MODIFIER | c.1204-1162dupT | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 8/17 | INFO_REALIGN_3_PRIME | chr15 | 41473442 | |||||
| chr15:41473442
|
GT | G | 26 | a0001c0001t0001g0005a0001c0001t0001g0030a0001c0001t0005g0210others(23): Show | 26 | HG01081.hp2 HG01106.hp2 HG01109.hp1 others(23): Show |
intron_variant | MODIFIER | c.1204-1162delT | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 8/17 | INFO_REALIGN_3_PRIME | chr15 | 41473442 | |||||
| chr15:41473620
|
C | T | 1 | a0001c0001t0003g0166 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.1204-1000C>T | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 8/17 | chr15 | 41473620 | ||||||
| chr15:41473762
|
C | T | 6 | a0001c0001t0001g0005a0001c0001t0009g0004a0001c0001t0009g0006others(3): Show | 6 | HG01109.hp1 HG01243.hp1 HG02145.hp2 others(3): Show |
intron_variant | MODIFIER | c.1204-858C>T | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 8/17 | chr15 | 41473762 | ||||||
| chr15:41473906
|
A | G | 1 | a0001c0001t0001g0068 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.1204-714A>G | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 8/17 | chr15 | 41473906 | ||||||
| chr15:41474225
|
A | G | 5 | a0001c0001t0006g0105a0001c0001t0006g0131a0001c0001t0006g0132others(2): Show | 5 | HG01168.hp2 HG02293.hp2 HG03927.hp2 others(2): Show |
intron_variant | MODIFIER | c.1204-395A>G | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 8/17 | chr15 | 41474225 | ||||||
| chr15:41474344
|
C | A | 6 | a0001c0001t0001g0005a0001c0001t0009g0004a0001c0001t0009g0006others(3): Show | 6 | HG01109.hp1 HG01243.hp1 HG02145.hp2 others(3): Show |
intron_variant | MODIFIER | c.1204-276C>A | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 8/17 | chr15 | 41474344 | ||||||
| chr15:41474599
|
C | T | 1 | a0001c0001t0002g0119 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.1204-21C>T | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 8/17 | chr15 | 41474599 | ||||||
| chr15:41474768
|
G | A | 224 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0011others(221): Show | 225 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(222): Show |
intron_variant | MODIFIER | c.1286+66G>A | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 9/17 | chr15 | 41474768 | ||||||
| chr15:41475117
|
C | T | 1 | a0001c0001t0001g0059 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.1287-408C>T | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 9/17 | chr15 | 41475117 | ||||||
| chr15:41475157
|
A | G | 6 | a0001c0001t0001g0005a0001c0001t0009g0004a0001c0001t0009g0006others(3): Show | 6 | HG01109.hp1 HG01243.hp1 HG02145.hp2 others(3): Show |
intron_variant | MODIFIER | c.1287-368A>G | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 9/17 | chr15 | 41475157 | ||||||
| chr15:41475359
|
A | G | 1 | a0001c0001t0001g0073 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.1287-166A>G | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 9/17 | chr15 | 41475359 | ||||||
| chr15:41476057
|
G | A | 15 | a0001c0001t0005g0210a0001c0001t0005g0211a0001c0001t0005g0212others(12): Show | 15 | HG01081.hp2 HG01106.hp2 HG01257.hp1 others(12): Show |
intron_variant | MODIFIER | c.1482+238G>A | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 11/17 | chr15 | 41476057 | ||||||
| chr15:41476096
|
G | A | 1 | a0001c0001t0001g0036 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.1482+277G>A | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 11/17 | chr15 | 41476096 | ||||||
| chr15:41476137
|
A | C | 1 | a0001c0001t0001g0077 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.1483-309A>C | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 11/17 | chr15 | 41476137 | ||||||
| chr15:41476138
|
A | G | 4 | a0001c0001t0005g0210a0001c0001t0005g0211a0001c0001t0005g0212others(1): Show | 4 | HG01891.hp1 HG03041.hp1 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.1483-308A>G | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 11/17 | chr15 | 41476138 | ||||||
| chr15:41476780
|
C | A | 1 | a0001c0001t0011g0200 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.1560+257C>A | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 12/17 | chr15 | 41476780 | ||||||
| chr15:41476830
|
A | G | 1 | a0001c0001t0001g0106 | 1 | NA19089.hp1 | intron_variant | MODIFIER | c.1560+307A>G | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 12/17 | chr15 | 41476830 | ||||||
| chr15:41477724
|
C | G | 1 | a0001c0001t0001g0046 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.1740+209C>G | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 14/17 | chr15 | 41477724 | ||||||
| chr15:41477754
|
T | A | 2 | a0001c0001t0004g0182a0001c0001t0004g0188 | 2 | HG01106.hp1 HG02486.hp2 |
intron_variant | MODIFIER | c.1740+239T>A | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 14/17 | chr15 | 41477754 | ||||||
| chr15:41477790
|
C | G | 3 | a0001c0001t0021g0148a0001c0001t0023g0146a0001c0001t0027g0147 | 3 | HG02976.hp2 HG03139.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.1740+275C>G | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 14/17 | chr15 | 41477790 | ||||||
| chr15:41478024
|
T | C | 3 | a0001c0001t0011g0200a0001c0001t0011g0201a0001c0001t0011g0202 | 3 | HG01496.hp1 HG02451.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.1740+509T>C | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 14/17 | chr15 | 41478024 | ||||||
| chr15:41478138
|
C | T | 1 | a0001c0001t0004g0192 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.1741-410C>T | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 14/17 | chr15 | 41478138 | ||||||
| chr15:41478305
|
G | A | 15 | a0001c0001t0005g0210a0001c0001t0005g0211a0001c0001t0005g0212others(12): Show | 15 | HG01081.hp2 HG01106.hp2 HG01257.hp1 others(12): Show |
intron_variant | MODIFIER | c.1741-243G>A | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 14/17 | chr15 | 41478305 | ||||||
| chr15:41478357
|
C | T | 1 | a0001c0001t0001g0033 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.1741-191C>T | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 14/17 | chr15 | 41478357 | ||||||
| chr15:41478410
|
T | TA | 8 | a0001c0001t0001g0005a0001c0001t0003g0002a0001c0001t0008g0014others(5): Show | 8 | HG01109.hp1 HG01243.hp1 HG02145.hp2 others(5): Show |
intron_variant | MODIFIER | c.1741-123dupA | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 14/17 | INFO_REALIGN_3_PRIME | chr15 | 41478410 | |||||
| chr15:41478441
|
C | CT | 20 | a0001c0001t0002g0049a0001c0001t0002g0123a0001c0001t0005g0210others(17): Show | 20 | HG01081.hp2 HG01106.hp2 HG01257.hp1 others(17): Show |
intron_variant | MODIFIER | c.1741-95dupT | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 14/17 | INFO_REALIGN_3_PRIME | chr15 | 41478441 | |||||
| chr15:41478943
|
C | CT | 24 | a0001c0001t0001g0080a0001c0001t0002g0113a0001c0001t0003g0169others(21): Show | 24 | HG01081.hp2 HG01106.hp2 HG01257.hp1 others(21): Show |
intron_variant | MODIFIER | c.1819-142dupT | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 15/17 | INFO_REALIGN_3_PRIME | chr15 | 41478943 | |||||
| chr15:41479393
|
G | A | 90 | a0001c0001t0001g0005a0001c0001t0003g0002a0001c0001t0003g0017others(87): Show | 90 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(87): Show |
intron_variant | MODIFIER | c.1914+195G>A | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 16/17 | chr15 | 41479393 | ||||||
| chr15:41479432
|
A | G | 3 | a0001c0001t0011g0023a0001c0001t0014g0199a0001c0001t0014g0209 | 3 | HG02572.hp2 HG02615.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.1914+234A>G | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 16/17 | chr15 | 41479432 | ||||||
| chr15:41479483
|
C | T | 1 | a0001c0001t0001g0042 | 1 | HG01257.hp2 | intron_variant | MODIFIER | c.1914+285C>T | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 16/17 | chr15 | 41479483 | ||||||
| chr15:41479487
|
G | A | 7 | a0001c0001t0003g0020a0001c0001t0003g0149a0001c0001t0003g0156others(4): Show | 7 | HG00323.hp2 HG00642.hp1 HG00741.hp2 others(4): Show |
intron_variant | MODIFIER | c.1914+289G>A | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 16/17 | chr15 | 41479487 | ||||||
| chr15:41479626
|
G | A | 1 | a0001c0001t0001g0011 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.1914+428G>A | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 16/17 | chr15 | 41479626 | ||||||
| chr15:41479627
|
G | C | 1 | a0001c0001t0005g0223 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1914+429G>C | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 16/17 | chr15 | 41479627 | ||||||
| chr15:41479642
|
C | A | 1 | a0001c0001t0003g0159 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.1914+444C>A | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 16/17 | chr15 | 41479642 | ||||||
| chr15:41479730
|
G | A | 1 | a0001c0001t0003g0167 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.1915-484G>A | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 16/17 | chr15 | 41479730 | ||||||
| chr15:41479732
|
G | A | 1 | a0001c0001t0004g0197 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.1915-482G>A | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 16/17 | chr15 | 41479732 | ||||||
| chr15:41479780
|
G | A | 3 | a0001c0001t0011g0200a0001c0001t0011g0201a0001c0001t0011g0202 | 3 | HG01496.hp1 HG02451.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.1915-434G>A | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 16/17 | chr15 | 41479780 | ||||||
| chr15:41479818
|
G | A | 29 | a0001c0001t0004g0177a0001c0001t0004g0178a0001c0001t0004g0179others(26): Show | 29 | HG00099.hp1 HG00609.hp1 HG01106.hp1 others(26): Show |
intron_variant | MODIFIER | c.1915-396G>A | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 16/17 | chr15 | 41479818 | ||||||
| chr15:41479864
|
C | CA | 7 | a0001c0001t0001g0033a0001c0001t0001g0048a0001c0001t0002g0126others(4): Show | 7 | HG00544.hp2 HG01081.hp1 HG01243.hp2 others(4): Show |
intron_variant | MODIFIER | c.1915-333dupA | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr15 | 41479864 | |||||
| chr15:41479864
|
CA | C | 56 | a0001c0001t0001g0005a0001c0001t0001g0069a0001c0001t0001g0106others(53): Show | 56 | HG00099.hp1 HG00609.hp1 HG01081.hp2 others(53): Show |
intron_variant | MODIFIER | c.1915-333delA | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr15 | 41479864 | |||||
| chr15:41479979
|
C | T | 2 | a0001c0001t0006g0105a0001c0001t0020g0116 | 2 | HG02293.hp2 HG04199.hp2 |
intron_variant | MODIFIER | c.1915-235C>T | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 16/17 | chr15 | 41479979 | ||||||
| chr15:41480004
|
A | C | 23 | a0001c0001t0003g0017a0001c0001t0003g0018a0001c0001t0003g0019others(20): Show | 23 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(20): Show |
intron_variant | MODIFIER | c.1915-210A>C | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 16/17 | chr15 | 41480004 | ||||||
| chr15:41480010
|
G | C | 1 | a0001c0001t0001g0071 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.1915-204G>C | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 16/17 | chr15 | 41480010 | ||||||
| chr15:41480141
|
G | A | 3 | a0001c0001t0011g0023a0001c0001t0014g0199a0001c0001t0014g0209 | 3 | HG02572.hp2 HG02615.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.1915-73G>A | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 16/17 | chr15 | 41480141 | ||||||
| chr15:41480176
|
T | G | 1 | a0001c0001t0001g0033 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.1915-38T>G | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 16/17 | chr15 | 41480176 | ||||||
| chr15:41480425
|
G | A | 6 | a0001c0001t0001g0005a0001c0001t0009g0004a0001c0001t0009g0006others(3): Show | 6 | HG01109.hp1 HG01243.hp1 HG02145.hp2 others(3): Show |
intron_variant | MODIFIER | c.2026+100G>A | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 17/17 | chr15 | 41480425 | ||||||
| chr15:41480466
|
T | C | 12 | a0001c0001t0001g0095a0001c0001t0005g0210a0001c0001t0005g0211others(9): Show | 12 | HG01496.hp1 HG01891.hp1 HG02451.hp2 others(9): Show |
intron_variant | MODIFIER | c.2027-115T>C | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 17/17 | chr15 | 41480466 | ||||||
| chr15:41480495
|
G | A | 23 | a0001c0001t0003g0017a0001c0001t0003g0018a0001c0001t0003g0019others(20): Show | 23 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(20): Show |
intron_variant | MODIFIER | c.2027-86G>A | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 17/17 | chr15 | 41480495 | ||||||
| chr15:41480554
|
C | T | 1 | a0001c0001t0002g0049 | 1 | NA19089.hp2 | intron_variant | MODIFIER | c.2027-27C>T | RTF1 | ENSG00000137815.15 | transcript | ENST00000389629.9 | protein_coding | 17/17 | chr15 | 41480554 |