Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| geneid | 79836 |
|---|---|
| ensemblid | ENSG00000175556.17 |
| hgncid | 21152 |
| symbol | LONRF3 |
| name | LON peptidase N-terminal domain and ring finger 3 |
| refseq_nuc | NM_001031855.3 |
| refseq_prot | NP_001027026.1 |
| ensembl_nuc | ENST00000371628.8 |
| ensembl_prot | ENSP00000360690.3 |
| mane_status | MANE Select |
| chr | chrX |
| start | 118974618 |
| end | 119018355 |
| strand | + |
| ver | v1.2 |
| region | chrX:118974618-119018355 |
| region5000 | chrX:118969618-119023355 |
| regionname0 | LONRF3_chrX_118974618_119018355 |
| regionname5000 | LONRF3_chrX_118969618_119023355 |
| 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 | 759 | 301 | 70 | 49 | 137 | 11 | 32 | 110 | LONRF3_chrX_118969618_119023355 | LONRF3 | copy fasta | chrX | 118969618 | 119023355 |
| a0002 | 0/0 | 759 | 4 | 4 | 0 | 0 | 0 | 0 | 0 | LONRF3_chrX_118969618_119023355 | LONRF3 | copy fasta | chrX | 118969618 | 119023355 |
| a0003 | 0/0 | 759 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | LONRF3_chrX_118969618_119023355 | LONRF3 | copy fasta | chrX | 118969618 | 119023355 |
| a0004 | 0/0 | 671 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | LONRF3_chrX_118969618_119023355 | LONRF3 | copy fasta | chrX | 118969618 | 119023355 |
| a0005 | 0/0 | 734 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | LONRF3_chrX_118969618_119023355 | LONRF3 | copy fasta | chrX | 118969618 | 119023355 |
| a0006 | 0/0 | 463 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | LONRF3_chrX_118969618_119023355 | LONRF3 | copy fasta | chrX | 118969618 | 119023355 |
| chapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| c0001 | 0/1 | 2280 | 143 | 7 | 26 | 95 | 5 | 9 | LONRF3_chrX_118969618_119023355 | LONRF3 | copy fasta | chrX | 118969618 | 119023355 |
| c0002 | 0/0 | 2280 | 104 | 44 | 12 | 29 | 5 | 14 | LONRF3_chrX_118969618_119023355 | LONRF3 | copy fasta | chrX | 118969618 | 119023355 |
| c0003 | 1/0 | 2280 | 25 | 2 | 9 | 7 | 1 | 5 | LONRF3_chrX_118969618_119023355 | LONRF3 | copy fasta | chrX | 118969618 | 119023355 |
| c0004 | 0/0 | 2280 | 20 | 10 | 1 | 5 | 0 | 4 | LONRF3_chrX_118969618_119023355 | LONRF3 | copy fasta | chrX | 118969618 | 119023355 |
| c0005 | 0/0 | 2280 | 7 | 6 | 1 | 0 | 0 | 0 | LONRF3_chrX_118969618_119023355 | LONRF3 | copy fasta | chrX | 118969618 | 119023355 |
| c0006 | 0/0 | 2280 | 4 | 4 | 0 | 0 | 0 | 0 | LONRF3_chrX_118969618_119023355 | LONRF3 | copy fasta | chrX | 118969618 | 119023355 |
| c0007 | 0/0 | 2280 | 1 | 0 | 1 | 0 | 0 | 0 | LONRF3_chrX_118969618_119023355 | LONRF3 | copy fasta | chrX | 118969618 | 119023355 |
| c0008 | 0/0 | 2281 | 1 | 0 | 0 | 1 | 0 | 0 | LONRF3_chrX_118969618_119023355 | LONRF3 | copy fasta | chrX | 118969618 | 119023355 |
| c0009 | 0/0 | 2280 | 1 | 0 | 0 | 1 | 0 | 0 | LONRF3_chrX_118969618_119023355 | LONRF3 | copy fasta | chrX | 118969618 | 119023355 |
| c0010 | 0/0 | 2279 | 1 | 0 | 0 | 1 | 0 | 0 | LONRF3_chrX_118969618_119023355 | LONRF3 | copy fasta | chrX | 118969618 | 119023355 |
| c0011 | 0/0 | 2280 | 1 | 1 | 0 | 0 | 0 | 0 | LONRF3_chrX_118969618_119023355 | LONRF3 | copy fasta | chrX | 118969618 | 119023355 |
| c0012 | 0/0 | 2281 | 1 | 0 | 0 | 1 | 0 | 0 | LONRF3_chrX_118969618_119023355 | LONRF3 | copy fasta | chrX | 118969618 | 119023355 |
| thapid | grch38chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| t0001 | 1/1 | 829 | 234 | 65 | 44 | 84 | 10 | 29 | LONRF3_chrX_118969618_119023355 | LONRF3 | copy fasta | chrX | 118969618 | 119023355 |
| t0002 | 0/0 | 828 | 64 | 0 | 6 | 54 | 1 | 3 | LONRF3_chrX_118969618_119023355 | LONRF3 | copy fasta | chrX | 118969618 | 119023355 |
| t0003 | 0/0 | 829 | 4 | 4 | 0 | 0 | 0 | 0 | LONRF3_chrX_118969618_119023355 | LONRF3 | copy fasta | chrX | 118969618 | 119023355 |
| t0004 | 0/0 | 829 | 2 | 2 | 0 | 0 | 0 | 0 | LONRF3_chrX_118969618_119023355 | LONRF3 | copy fasta | chrX | 118969618 | 119023355 |
| t0005 | 0/0 | 828 | 1 | 1 | 0 | 0 | 0 | 0 | LONRF3_chrX_118969618_119023355 | LONRF3 | copy fasta | chrX | 118969618 | 119023355 |
| t0006 | 0/0 | 829 | 1 | 1 | 0 | 0 | 0 | 0 | LONRF3_chrX_118969618_119023355 | LONRF3 | copy fasta | chrX | 118969618 | 119023355 |
| t0007 | 0/0 | 825 | 1 | 0 | 0 | 1 | 0 | 0 | LONRF3_chrX_118969618_119023355 | LONRF3 | copy fasta | chrX | 118969618 | 119023355 |
| t0008 | 0/0 | 829 | 1 | 1 | 0 | 0 | 0 | 0 | LONRF3_chrX_118969618_119023355 | LONRF3 | copy fasta | chrX | 118969618 | 119023355 |
| t0009 | 0/0 | 829 | 1 | 0 | 0 | 1 | 0 | 0 | LONRF3_chrX_118969618_119023355 | LONRF3 | copy fasta | chrX | 118969618 | 119023355 |
| 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 | 4 | 0 | 0 | 3 | 0 | 1 | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| g0002 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| g0003 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| g0004 | 0/0 | 3 | 0 | 0 | 0 | 2 | 1 | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| g0005 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| g0006 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| g0007 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| g0008 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| g0009 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| g0010 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| g0011 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| g0012 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| g0013 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| g0014 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| g0015 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| g0016 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| g0017 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| g0018 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| g0019 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| g0020 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| g0021 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| g0023 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| g0034 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| g0037 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| g0047 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| g0052 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| g0057 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| g0059 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| g0076 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| g0083 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| g0089 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| g0094 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| g0098 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| g0104 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| g0110 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| g0118 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| g0125 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| g0126 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| g0127 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| g0129 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| g0130 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| g0133 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| g0135 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| g0137 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| g0140 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| g0141 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| g0143 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| g0149 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| g0151 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| g0154 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| g0155 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| g0156 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| g0159 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| g0160 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| g0165 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| g0167 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| g0171 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| g0172 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| g0174 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| g0175 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| g0177 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| g0178 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| g0179 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| g0180 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| g0181 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| g0182 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| g0183 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| g0189 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| g0204 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| g0205 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| g0211 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| g0221 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| g0223 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| g0225 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| g0230 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| g0231 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| g0238 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| g0239 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| g0240 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| g0242 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| g0243 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| g0244 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| g0245 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| g0246 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| g0248 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| g0249 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| g0250 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| g0252 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| g0254 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| g0258 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| g0259 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| g0262 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| g0263 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| g0264 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| g0265 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| g0266 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| g0267 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| g0268 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| g0271 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| g0272 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| g0273 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| g0274 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| g0276 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| g0277 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| g0278 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| g0279 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| achapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 0/1 | 2280 | 143 | 7 | 26 | 95 | 5 | 9 | LONRF3_chrX_118969618_119023355 | LONRF3 | copy fasta | chrX | 118969618 | 119023355 |
| a0001c0002 | 0/0 | 2280 | 104 | 44 | 12 | 29 | 5 | 14 | LONRF3_chrX_118969618_119023355 | LONRF3 | copy fasta | chrX | 118969618 | 119023355 |
| a0001c0003 | 1/0 | 2280 | 25 | 2 | 9 | 7 | 1 | 5 | LONRF3_chrX_118969618_119023355 | LONRF3 | copy fasta | chrX | 118969618 | 119023355 |
| a0001c0004 | 0/0 | 2280 | 20 | 10 | 1 | 5 | 0 | 4 | LONRF3_chrX_118969618_119023355 | LONRF3 | copy fasta | chrX | 118969618 | 119023355 |
| a0001c0005 | 0/0 | 2280 | 7 | 6 | 1 | 0 | 0 | 0 | LONRF3_chrX_118969618_119023355 | LONRF3 | copy fasta | chrX | 118969618 | 119023355 |
| a0001c0009 | 0/0 | 2280 | 1 | 0 | 0 | 1 | 0 | 0 | LONRF3_chrX_118969618_119023355 | LONRF3 | copy fasta | chrX | 118969618 | 119023355 |
| a0001c0011 | 0/0 | 2280 | 1 | 1 | 0 | 0 | 0 | 0 | LONRF3_chrX_118969618_119023355 | LONRF3 | copy fasta | chrX | 118969618 | 119023355 |
| a0002c0006 | 0/0 | 2280 | 4 | 4 | 0 | 0 | 0 | 0 | LONRF3_chrX_118969618_119023355 | LONRF3 | copy fasta | chrX | 118969618 | 119023355 |
| a0003c0007 | 0/0 | 2280 | 1 | 0 | 1 | 0 | 0 | 0 | LONRF3_chrX_118969618_119023355 | LONRF3 | copy fasta | chrX | 118969618 | 119023355 |
| a0004c0008 | 0/0 | 2281 | 1 | 0 | 0 | 1 | 0 | 0 | LONRF3_chrX_118969618_119023355 | LONRF3 | copy fasta | chrX | 118969618 | 119023355 |
| a0005c0010 | 0/0 | 2279 | 1 | 0 | 0 | 1 | 0 | 0 | LONRF3_chrX_118969618_119023355 | LONRF3 | copy fasta | chrX | 118969618 | 119023355 |
| a0006c0012 | 0/0 | 2281 | 1 | 0 | 0 | 1 | 0 | 0 | LONRF3_chrX_118969618_119023355 | LONRF3 | copy fasta | chrX | 118969618 | 119023355 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/1 | 3108 | 88 | 7 | 20 | 48 | 4 | 8 | LONRF3_chrX_118969618_119023355 | LONRF3 | copy fasta | chrX | 118969618 | 119023355 |
| a0001c0001t0002 | 0/0 | 3107 | 54 | 0 | 6 | 46 | 1 | 1 | LONRF3_chrX_118969618_119023355 | LONRF3 | copy fasta | chrX | 118969618 | 119023355 |
| a0001c0001t0009 | 0/0 | 3108 | 1 | 0 | 0 | 1 | 0 | 0 | LONRF3_chrX_118969618_119023355 | LONRF3 | copy fasta | chrX | 118969618 | 119023355 |
| a0001c0002t0001 | 0/0 | 3108 | 96 | 36 | 12 | 29 | 5 | 14 | LONRF3_chrX_118969618_119023355 | LONRF3 | copy fasta | chrX | 118969618 | 119023355 |
| a0001c0002t0003 | 0/0 | 3108 | 3 | 3 | 0 | 0 | 0 | 0 | LONRF3_chrX_118969618_119023355 | LONRF3 | copy fasta | chrX | 118969618 | 119023355 |
| a0001c0002t0004 | 0/0 | 3108 | 2 | 2 | 0 | 0 | 0 | 0 | LONRF3_chrX_118969618_119023355 | LONRF3 | copy fasta | chrX | 118969618 | 119023355 |
| a0001c0002t0005 | 0/0 | 3107 | 1 | 1 | 0 | 0 | 0 | 0 | LONRF3_chrX_118969618_119023355 | LONRF3 | copy fasta | chrX | 118969618 | 119023355 |
| a0001c0002t0006 | 0/0 | 3108 | 1 | 1 | 0 | 0 | 0 | 0 | LONRF3_chrX_118969618_119023355 | LONRF3 | copy fasta | chrX | 118969618 | 119023355 |
| a0001c0002t0008 | 0/0 | 3108 | 1 | 1 | 0 | 0 | 0 | 0 | LONRF3_chrX_118969618_119023355 | LONRF3 | copy fasta | chrX | 118969618 | 119023355 |
| a0001c0003t0001 | 1/0 | 3108 | 16 | 2 | 9 | 0 | 1 | 3 | LONRF3_chrX_118969618_119023355 | LONRF3 | copy fasta | chrX | 118969618 | 119023355 |
| a0001c0003t0002 | 0/0 | 3107 | 9 | 0 | 0 | 7 | 0 | 2 | LONRF3_chrX_118969618_119023355 | LONRF3 | copy fasta | chrX | 118969618 | 119023355 |
| a0001c0004t0001 | 0/0 | 3108 | 20 | 10 | 1 | 5 | 0 | 4 | LONRF3_chrX_118969618_119023355 | LONRF3 | copy fasta | chrX | 118969618 | 119023355 |
| a0001c0005t0001 | 0/0 | 3108 | 7 | 6 | 1 | 0 | 0 | 0 | LONRF3_chrX_118969618_119023355 | LONRF3 | copy fasta | chrX | 118969618 | 119023355 |
| a0001c0009t0002 | 0/0 | 3107 | 1 | 0 | 0 | 1 | 0 | 0 | LONRF3_chrX_118969618_119023355 | LONRF3 | copy fasta | chrX | 118969618 | 119023355 |
| a0001c0011t0003 | 0/0 | 3108 | 1 | 1 | 0 | 0 | 0 | 0 | LONRF3_chrX_118969618_119023355 | LONRF3 | copy fasta | chrX | 118969618 | 119023355 |
| a0002c0006t0001 | 0/0 | 3108 | 4 | 4 | 0 | 0 | 0 | 0 | LONRF3_chrX_118969618_119023355 | LONRF3 | copy fasta | chrX | 118969618 | 119023355 |
| a0003c0007t0001 | 0/0 | 3108 | 1 | 0 | 1 | 0 | 0 | 0 | LONRF3_chrX_118969618_119023355 | LONRF3 | copy fasta | chrX | 118969618 | 119023355 |
| a0004c0008t0001 | 0/0 | 3109 | 1 | 0 | 0 | 1 | 0 | 0 | LONRF3_chrX_118969618_119023355 | LONRF3 | copy fasta | chrX | 118969618 | 119023355 |
| a0005c0010t0007 | 0/0 | 3103 | 1 | 0 | 0 | 1 | 0 | 0 | LONRF3_chrX_118969618_119023355 | LONRF3 | copy fasta | chrX | 118969618 | 119023355 |
| a0006c0012t0001 | 0/0 | 3109 | 1 | 0 | 0 | 1 | 0 | 0 | LONRF3_chrX_118969618_119023355 | LONRF3 | copy fasta | chrX | 118969618 | 119023355 |
| actghapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| a0001c0001t0001g0002 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| a0001c0001t0001g0006 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| a0001c0001t0001g0007 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| a0001c0001t0001g0013 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| a0001c0001t0001g0020 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| a0001c0001t0001g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| a0001c0001t0001g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| a0001c0001t0001g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| a0001c0001t0001g0047 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| a0001c0001t0001g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| a0001c0001t0001g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| a0001c0001t0001g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| a0001c0001t0001g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| a0001c0001t0001g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| a0001c0001t0001g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| a0001c0001t0001g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| a0001c0001t0001g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| a0001c0001t0001g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| a0001c0001t0001g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| a0001c0001t0001g0204 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| a0001c0001t0001g0205 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| a0001c0001t0001g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| a0001c0001t0001g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| a0001c0001t0001g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| a0001c0001t0001g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| a0001c0001t0001g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| a0001c0001t0001g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| a0001c0001t0001g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| a0001c0001t0001g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| a0001c0001t0001g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| a0001c0001t0001g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| a0001c0001t0001g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| a0001c0001t0001g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| a0001c0001t0001g0221 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| a0001c0001t0001g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| a0001c0001t0001g0223 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| a0001c0001t0001g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| a0001c0001t0001g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| a0001c0001t0001g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| a0001c0001t0001g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| a0001c0001t0001g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| a0001c0001t0001g0230 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| a0001c0001t0001g0231 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| a0001c0001t0001g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| a0001c0001t0001g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| a0001c0001t0001g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| a0001c0001t0001g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| a0001c0001t0001g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| a0001c0001t0001g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| a0001c0001t0001g0238 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| a0001c0001t0001g0239 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| a0001c0001t0001g0240 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| a0001c0001t0001g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| a0001c0001t0001g0242 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| a0001c0001t0001g0243 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| a0001c0001t0001g0244 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| a0001c0001t0001g0245 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| a0001c0001t0001g0246 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| a0001c0001t0001g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| a0001c0001t0001g0248 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| a0001c0001t0001g0249 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| a0001c0001t0001g0250 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| a0001c0001t0001g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| a0001c0001t0001g0254 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| a0001c0001t0001g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| a0001c0001t0001g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| a0001c0001t0001g0259 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| a0001c0001t0001g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| a0001c0001t0001g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| a0001c0001t0001g0262 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| a0001c0001t0001g0263 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| a0001c0001t0001g0264 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| a0001c0001t0001g0268 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| a0001c0001t0001g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| a0001c0001t0001g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| a0001c0001t0001g0272 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| a0001c0001t0001g0273 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| a0001c0001t0001g0274 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| a0001c0001t0001g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| a0001c0001t0002g0001 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| a0001c0001t0002g0010 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| a0001c0001t0002g0011 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| a0001c0001t0002g0012 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| a0001c0001t0002g0016 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| a0001c0001t0002g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| a0001c0001t0002g0052 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| a0001c0001t0002g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| a0001c0001t0002g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| a0001c0001t0002g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| a0001c0001t0002g0057 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| a0001c0001t0002g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| a0001c0001t0002g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| a0001c0001t0002g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| a0001c0001t0002g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| a0001c0001t0002g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| a0001c0001t0002g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| a0001c0001t0002g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| a0001c0001t0002g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| a0001c0001t0002g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| a0001c0001t0002g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| a0001c0001t0002g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| a0001c0001t0002g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| a0001c0001t0002g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| a0001c0001t0002g0076 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| a0001c0001t0002g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| a0001c0001t0002g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| a0001c0001t0002g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| a0001c0001t0002g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| a0001c0001t0002g0083 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| a0001c0001t0002g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| a0001c0001t0002g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| a0001c0001t0002g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| a0001c0001t0002g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| a0001c0001t0002g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| a0001c0001t0002g0089 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| a0001c0001t0002g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| a0001c0001t0002g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| a0001c0001t0002g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| a0001c0001t0002g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| a0001c0001t0002g0104 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| a0001c0001t0002g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| a0001c0001t0002g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| a0001c0001t0002g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| a0001c0001t0002g0110 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| a0001c0001t0002g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| a0001c0001t0002g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| a0001c0001t0002g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| a0001c0001t0002g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| a0001c0001t0009g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| a0001c0002t0001g0003 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| a0001c0002t0001g0004 | 0/0 | 3 | 0 | 0 | 0 | 2 | 1 | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| a0001c0002t0001g0005 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| a0001c0002t0001g0008 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| a0001c0002t0001g0009 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| a0001c0002t0001g0017 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| a0001c0002t0001g0018 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| a0001c0002t0001g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| a0001c0002t0001g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| a0001c0002t0001g0023 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| a0001c0002t0001g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| a0001c0002t0001g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| a0001c0002t0001g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| a0001c0002t0001g0034 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| a0001c0002t0001g0037 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| a0001c0002t0001g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| a0001c0002t0001g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| a0001c0002t0001g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| a0001c0002t0001g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| a0001c0002t0001g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| a0001c0002t0001g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| a0001c0002t0001g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| a0001c0002t0001g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| a0001c0002t0001g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| a0001c0002t0001g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| a0001c0002t0001g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| a0001c0002t0001g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| a0001c0002t0001g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| a0001c0002t0001g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| a0001c0002t0001g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| a0001c0002t0001g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| a0001c0002t0001g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| a0001c0002t0001g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| a0001c0002t0001g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| a0001c0002t0001g0125 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| a0001c0002t0001g0127 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| a0001c0002t0001g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| a0001c0002t0001g0130 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| a0001c0002t0001g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| a0001c0002t0001g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| a0001c0002t0001g0133 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| a0001c0002t0001g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| a0001c0002t0001g0135 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| a0001c0002t0001g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| a0001c0002t0001g0137 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| a0001c0002t0001g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| a0001c0002t0001g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| a0001c0002t0001g0140 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| a0001c0002t0001g0141 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| a0001c0002t0001g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| a0001c0002t0001g0143 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| a0001c0002t0001g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| a0001c0002t0001g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| a0001c0002t0001g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| a0001c0002t0001g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| a0001c0002t0001g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| a0001c0002t0001g0149 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| a0001c0002t0001g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| a0001c0002t0001g0151 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| a0001c0002t0001g0154 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| a0001c0002t0001g0155 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| a0001c0002t0001g0156 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| a0001c0002t0001g0159 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| a0001c0002t0001g0160 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| a0001c0002t0001g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| a0001c0002t0001g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| a0001c0002t0001g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| a0001c0002t0001g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| a0001c0002t0001g0165 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| a0001c0002t0001g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| a0001c0002t0001g0167 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| a0001c0002t0001g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| a0001c0002t0001g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| a0001c0002t0001g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| a0001c0002t0001g0172 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| a0001c0002t0001g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| a0001c0002t0001g0177 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| a0001c0002t0001g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| a0001c0002t0001g0189 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| a0001c0002t0001g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| a0001c0002t0001g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| a0001c0002t0001g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| a0001c0002t0001g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| a0001c0002t0001g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| a0001c0002t0001g0267 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| a0001c0002t0001g0276 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| a0001c0002t0003g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| a0001c0002t0003g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| a0001c0002t0003g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| a0001c0002t0004g0021 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| a0001c0002t0005g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| a0001c0002t0006g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| a0001c0002t0008g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| a0001c0003t0001g0094 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| a0001c0003t0001g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| a0001c0003t0001g0098 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| a0001c0003t0001g0118 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| a0001c0003t0001g0171 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| a0001c0003t0001g0174 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| a0001c0003t0001g0178 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| a0001c0003t0001g0179 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| a0001c0003t0001g0180 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| a0001c0003t0001g0181 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| a0001c0003t0001g0182 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| a0001c0003t0001g0183 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| a0001c0003t0001g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| a0001c0003t0001g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| a0001c0003t0001g0252 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| a0001c0003t0001g0266 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| a0001c0003t0002g0001 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| a0001c0003t0002g0013 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| a0001c0003t0002g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| a0001c0003t0002g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| a0001c0003t0002g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| a0001c0003t0002g0059 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| a0001c0003t0002g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| a0001c0003t0002g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| a0001c0003t0002g0271 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| a0001c0004t0001g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| a0001c0004t0001g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| a0001c0004t0001g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| a0001c0004t0001g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| a0001c0004t0001g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| a0001c0004t0001g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| a0001c0004t0001g0126 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| a0001c0004t0001g0129 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| a0001c0004t0001g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| a0001c0004t0001g0175 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| a0001c0004t0001g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| a0001c0004t0001g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| a0001c0004t0001g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| a0001c0004t0001g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| a0001c0004t0001g0211 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| a0001c0004t0001g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| a0001c0004t0001g0258 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| a0001c0004t0001g0277 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| a0001c0004t0001g0278 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| a0001c0004t0001g0279 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| a0001c0005t0001g0014 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| a0001c0005t0001g0015 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| a0001c0005t0001g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| a0001c0005t0001g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| a0001c0005t0001g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| a0001c0009t0002g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| a0001c0011t0003g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| a0002c0006t0001g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| a0002c0006t0001g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| a0002c0006t0001g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| a0002c0006t0001g0265 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| a0003c0007t0001g0225 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| a0004c0008t0001g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| a0005c0010t0007g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| a0006c0012t0001g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0002 | t0001 | g0167 | EUR | GBR | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| HG00099 | hp2 | a0001 | c0001 | t0002 | g0110 | EUR | GBR | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| HG00140 | hp1 | a0001 | c0002 | t0001 | g0151 | EUR | GBR | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| HG00280 | hp1 | a0001 | c0001 | t0001 | g0221 | EUR | FIN | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| HG00323 | hp1 | a0001 | c0002 | t0001 | g0137 | EUR | FIN | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| HG00323 | hp2 | a0001 | c0001 | t0001 | g0254 | EUR | FIN | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| HG00408 | hp1 | a0001 | c0002 | t0001 | g0042 | EAS | CHS | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| HG00408 | hp2 | a0001 | c0001 | t0001 | g0013 | EAS | CHS | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| HG00423 | hp1 | a0001 | c0002 | t0001 | g0045 | EAS | CHS | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| HG00423 | hp2 | a0001 | c0001 | t0002 | g0086 | EAS | CHS | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| HG00438 | hp1 | a0001 | c0001 | t0001 | g0241 | EAS | CHS | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| HG00438 | hp2 | a0001 | c0001 | t0002 | g0068 | EAS | CHS | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| HG00544 | hp1 | a0001 | c0001 | t0001 | g0212 | EAS | CHS | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| HG00544 | hp2 | a0001 | c0002 | t0001 | g0008 | EAS | CHS | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| HG00597 | hp1 | a0001 | c0001 | t0001 | g0027 | EAS | CHS | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| HG00597 | hp2 | a0001 | c0001 | t0002 | g0050 | EAS | CHS | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| HG00609 | hp1 | a0001 | c0001 | t0001 | g0257 | EAS | CHS | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| HG00621 | hp1 | a0001 | c0001 | t0002 | g0088 | EAS | CHS | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| HG00639 | hp1 | a0001 | c0005 | t0001 | g0014 | AMR | PUR | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| HG00639 | hp2 | a0001 | c0002 | t0001 | g0267 | AMR | PUR | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| HG00642 | hp1 | a0001 | c0004 | t0001 | g0126 | AMR | PUR | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| HG00673 | hp1 | a0001 | c0003 | t0002 | g0070 | EAS | CHS | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| HG00733 | hp1 | a0001 | c0001 | t0001 | g0243 | AMR | PUR | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| HG00733 | hp2 | a0001 | c0002 | t0001 | g0143 | AMR | PUR | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| HG00738 | hp1 | a0001 | c0001 | t0001 | g0244 | AMR | PUR | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| HG00741 | hp1 | a0001 | c0003 | t0001 | g0183 | AMR | PUR | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| HG00741 | hp2 | a0001 | c0002 | t0001 | g0133 | AMR | PUR | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| HG01069 | hp1 | a0001 | c0002 | t0001 | g0018 | AMR | PUR | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| HG01070 | hp1 | a0001 | c0001 | t0001 | g0272 | AMR | PUR | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| HG01070 | hp2 | a0001 | c0002 | t0001 | g0130 | AMR | PUR | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| HG01071 | hp1 | a0001 | c0001 | t0001 | g0273 | AMR | PUR | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| HG01071 | hp2 | a0001 | c0002 | t0001 | g0018 | AMR | PUR | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| HG01074 | hp1 | a0001 | c0003 | t0001 | g0180 | AMR | PUR | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| HG01081 | hp1 | a0001 | c0001 | t0001 | g0006 | AMR | PUR | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| HG01081 | hp2 | a0001 | c0001 | t0001 | g0245 | AMR | PUR | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| HG01099 | hp1 | a0001 | c0003 | t0001 | g0097 | AMR | PUR | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| HG01106 | hp1 | a0001 | c0002 | t0001 | g0023 | AMR | PUR | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| HG01109 | hp1 | a0001 | c0002 | t0001 | g0165 | AMR | PUR | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| HG01167 | hp1 | a0001 | c0003 | t0001 | g0098 | AMR | PUR | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| HG01168 | hp1 | a0001 | c0003 | t0001 | g0181 | AMR | PUR | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| HG01168 | hp2 | a0003 | c0007 | t0001 | g0225 | AMR | PUR | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| HG01169 | hp1 | a0001 | c0003 | t0001 | g0179 | AMR | PUR | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| HG01169 | hp2 | a0001 | c0003 | t0001 | g0094 | AMR | PUR | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| HG01192 | hp1 | a0001 | c0002 | t0001 | g0125 | AMR | PUR | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| HG01243 | hp1 | a0001 | c0002 | t0001 | g0189 | AMR | PUR | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| HG01255 | hp1 | a0001 | c0001 | t0001 | g0259 | AMR | CLM | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| HG01256 | hp1 | a0001 | c0003 | t0001 | g0171 | AMR | CLM | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| HG01257 | hp1 | a0001 | c0002 | t0001 | g0155 | AMR | CLM | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| HG01257 | hp2 | a0001 | c0001 | t0001 | g0205 | AMR | CLM | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| HG01258 | hp1 | a0001 | c0001 | t0001 | g0204 | AMR | CLM | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| HG01261 | hp1 | a0001 | c0001 | t0002 | g0012 | AMR | CLM | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| HG01346 | hp1 | a0001 | c0001 | t0002 | g0083 | AMR | CLM | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| HG01346 | hp2 | a0001 | c0001 | t0001 | g0230 | AMR | CLM | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| HG01358 | hp1 | a0001 | c0001 | t0001 | g0231 | AMR | CLM | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| HG01433 | hp1 | a0001 | c0003 | t0001 | g0252 | AMR | CLM | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| HG01515 | hp1 | a0001 | c0002 | t0001 | g0004 | EUR | IBS | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| HG01517 | hp1 | a0001 | c0003 | t0001 | g0266 | EUR | IBS | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| HG01517 | hp2 | a0001 | c0002 | t0001 | g0004 | EUR | IBS | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| HG01884 | hp1 | a0001 | c0004 | t0001 | g0095 | AFR | ACB | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| HG01884 | hp2 | a0001 | c0005 | t0001 | g0014 | AFR | ACB | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| HG01891 | hp1 | a0001 | c0002 | t0004 | g0021 | AFR | ACB | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| HG01891 | hp2 | a0001 | c0001 | t0001 | g0111 | AFR | ACB | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| HG01928 | hp1 | a0001 | c0001 | t0002 | g0057 | AMR | PEL | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| HG01934 | hp1 | a0001 | c0001 | t0001 | g0268 | AMR | PEL | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| HG01943 | hp1 | a0001 | c0001 | t0001 | g0006 | AMR | PEL | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| HG01952 | hp1 | a0001 | c0001 | t0001 | g0246 | AMR | PEL | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| HG01978 | hp1 | a0001 | c0001 | t0002 | g0104 | AMR | PEL | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| HG01978 | hp2 | a0001 | c0001 | t0001 | g0006 | AMR | PEL | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| HG01981 | hp1 | a0001 | c0002 | t0001 | g0127 | AMR | PEL | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| HG01981 | hp2 | a0001 | c0001 | t0002 | g0076 | AMR | PEL | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| HG01993 | hp1 | a0001 | c0001 | t0001 | g0248 | AMR | PEL | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| HG01993 | hp2 | a0001 | c0001 | t0002 | g0052 | AMR | PEL | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| HG02015 | hp1 | a0001 | c0001 | t0001 | g0100 | EAS | KHV | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| HG02027 | hp1 | a0001 | c0003 | t0002 | g0036 | EAS | KHV | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| HG02040 | hp1 | a0001 | c0001 | t0001 | g0064 | EAS | KHV | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| HG02055 | hp1 | a0001 | c0002 | t0001 | g0124 | AFR | ACB | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| HG02056 | hp1 | a0001 | c0001 | t0002 | g0016 | EAS | KHV | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| HG02071 | hp1 | a0001 | c0002 | t0001 | g0044 | EAS | KHV | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| HG02074 | hp1 | a0001 | c0002 | t0001 | g0041 | EAS | KHV | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| HG02083 | hp1 | a0001 | c0002 | t0001 | g0144 | EAS | KHV | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| HG02129 | hp1 | a0001 | c0001 | t0001 | g0251 | EAS | KHV | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| HG02132 | hp1 | a0001 | c0001 | t0001 | g0269 | EAS | KHV | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| HG02135 | hp1 | a0001 | c0002 | t0001 | g0147 | EAS | KHV | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| HG02145 | hp1 | a0001 | c0002 | t0001 | g0116 | AFR | ACB | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| HG02148 | hp1 | a0001 | c0001 | t0001 | g0242 | AMR | PEL | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| HG02148 | hp2 | a0001 | c0001 | t0001 | g0250 | AMR | PEL | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| HG02165 | hp1 | a0001 | c0001 | t0001 | g0255 | EAS | CDX | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| HG02165 | hp2 | a0001 | c0002 | t0001 | g0008 | EAS | CDX | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| HG02257 | hp1 | a0001 | c0002 | t0001 | g0193 | AFR | ACB | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| HG02257 | hp2 | a0001 | c0002 | t0001 | g0150 | AFR | ACB | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| HG02258 | hp1 | a0001 | c0004 | t0001 | g0277 | AFR | ACB | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| HG02280 | hp1 | a0001 | c0001 | t0001 | g0152 | AFR | ACB | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| HG02280 | hp2 | a0001 | c0001 | t0001 | g0107 | AFR | ACB | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| HG02451 | hp1 | a0001 | c0002 | t0001 | g0163 | AFR | ACB | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| HG02451 | hp2 | a0002 | c0006 | t0001 | g0157 | AFR | ACB | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| HG02572 | hp1 | a0001 | c0005 | t0001 | g0058 | AFR | GWD | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| HG02602 | hp1 | a0001 | c0002 | t0001 | g0149 | SAS | PJL | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| HG02615 | hp1 | a0001 | c0002 | t0001 | g0120 | AFR | GWD | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| HG02615 | hp2 | a0002 | c0006 | t0001 | g0158 | AFR | GWD | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| HG02622 | hp1 | a0001 | c0002 | t0003 | g0188 | AFR | GWD | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| HG02622 | hp2 | a0001 | c0004 | t0001 | g0192 | AFR | GWD | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| HG02630 | hp1 | a0001 | c0002 | t0006 | g0184 | AFR | GWD | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| HG02630 | hp2 | a0001 | c0002 | t0001 | g0132 | AFR | GWD | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| HG02647 | hp1 | a0001 | c0005 | t0001 | g0015 | AFR | GWD | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| HG02698 | hp1 | a0001 | c0003 | t0001 | g0118 | SAS | PJL | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| HG02717 | hp1 | a0001 | c0002 | t0001 | g0049 | AFR | GWD | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| HG02723 | hp1 | a0001 | c0002 | t0003 | g0187 | AFR | GWD | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| HG02723 | hp2 | a0001 | c0002 | t0001 | g0022 | AFR | GWD | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| HG02735 | hp1 | a0001 | c0002 | t0001 | g0140 | SAS | PJL | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| HG02738 | hp1 | a0001 | c0002 | t0001 | g0141 | SAS | PJL | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| HG02809 | hp1 | a0001 | c0002 | t0005 | g0028 | AFR | GWD | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| HG02809 | hp2 | a0001 | c0002 | t0001 | g0005 | AFR | GWD | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| HG02818 | hp1 | a0001 | c0002 | t0008 | g0186 | AFR | GWD | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| HG02818 | hp2 | a0001 | c0002 | t0001 | g0185 | AFR | GWD | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| HG02886 | hp1 | a0001 | c0002 | t0001 | g0024 | AFR | GWD | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| HG02886 | hp2 | a0001 | c0005 | t0001 | g0081 | AFR | GWD | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| HG02895 | hp1 | a0001 | c0002 | t0001 | g0191 | AFR | GWD | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| HG02896 | hp1 | a0001 | c0001 | t0001 | g0112 | AFR | GWD | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| HG02896 | hp2 | a0001 | c0002 | t0001 | g0139 | AFR | GWD | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| HG02897 | hp1 | a0001 | c0002 | t0001 | g0138 | AFR | GWD | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| HG02897 | hp2 | a0001 | c0002 | t0001 | g0190 | AFR | GWD | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| HG02922 | hp1 | a0001 | c0004 | t0001 | g0099 | AFR | ESN | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| HG02922 | hp2 | a0001 | c0002 | t0001 | g0017 | AFR | ESN | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| HG02965 | hp1 | a0001 | c0002 | t0001 | g0019 | AFR | ESN | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| HG02970 | hp1 | a0001 | c0002 | t0001 | g0195 | AFR | ESN | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| HG02970 | hp2 | a0001 | c0002 | t0001 | g0128 | AFR | ESN | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| HG02976 | hp1 | a0001 | c0004 | t0001 | g0102 | AFR | ESN | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| HG02976 | hp2 | a0001 | c0002 | t0001 | g0017 | AFR | ESN | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| HG03017 | hp1 | a0001 | c0002 | t0001 | g0154 | SAS | PJL | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| HG03041 | hp1 | a0001 | c0002 | t0001 | g0005 | AFR | GWD | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| HG03041 | hp2 | a0002 | c0006 | t0001 | g0265 | AFR | GWD | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| HG03098 | hp1 | a0002 | c0006 | t0001 | g0019 | AFR | MSL | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| HG03130 | hp1 | a0001 | c0005 | t0001 | g0015 | AFR | ESN | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| HG03139 | hp1 | a0001 | c0001 | t0001 | g0224 | AFR | ESN | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| HG03195 | hp1 | a0001 | c0002 | t0001 | g0196 | AFR | ESN | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| HG03195 | hp2 | a0001 | c0002 | t0004 | g0021 | AFR | ESN | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| HG03209 | hp1 | a0001 | c0002 | t0001 | g0043 | AFR | MSL | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| HG03225 | hp1 | a0001 | c0002 | t0001 | g0168 | AFR | MSL | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| HG03239 | hp1 | a0001 | c0003 | t0001 | g0178 | SAS | PJL | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| HG03239 | hp2 | a0001 | c0004 | t0001 | g0175 | SAS | PJL | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| HG03453 | hp1 | a0001 | c0004 | t0001 | g0197 | AFR | MSL | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| HG03453 | hp2 | a0001 | c0003 | t0001 | g0194 | AFR | MSL | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| HG03486 | hp1 | a0001 | c0002 | t0001 | g0122 | AFR | MSL | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| HG03486 | hp2 | a0001 | c0001 | t0001 | g0109 | AFR | MSL | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| HG03490 | hp1 | a0001 | c0002 | t0001 | g0172 | SAS | PJL | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| HG03491 | hp1 | a0001 | c0001 | t0001 | g0020 | SAS | PJL | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| HG03491 | hp2 | a0001 | c0002 | t0001 | g0034 | SAS | PJL | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| HG03492 | hp1 | a0001 | c0001 | t0001 | g0020 | SAS | PJL | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| HG03516 | hp1 | a0001 | c0002 | t0001 | g0123 | AFR | ESN | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| HG03516 | hp2 | a0001 | c0002 | t0003 | g0025 | AFR | ESN | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| HG03540 | hp1 | a0001 | c0004 | t0001 | g0101 | AFR | GWD | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| HG03540 | hp2 | a0001 | c0004 | t0001 | g0051 | AFR | GWD | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| HG03579 | hp1 | a0001 | c0002 | t0001 | g0117 | AFR | MSL | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| HG03654 | hp1 | a0001 | c0002 | t0001 | g0156 | SAS | PJL | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| HG03669 | hp1 | a0001 | c0002 | t0001 | g0135 | SAS | PJL | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| HG03669 | hp2 | a0001 | c0003 | t0002 | g0059 | SAS | PJL | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| HG03688 | hp1 | a0001 | c0003 | t0002 | g0271 | SAS | STU | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| HG03704 | hp1 | a0001 | c0004 | t0001 | g0129 | SAS | PJL | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| HG03704 | hp2 | a0001 | c0004 | t0001 | g0211 | SAS | PJL | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| HG03710 | hp1 | a0001 | c0002 | t0001 | g0160 | SAS | PJL | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| HG03831 | hp1 | a0001 | c0001 | t0001 | g0263 | SAS | BEB | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| HG03831 | hp2 | a0001 | c0002 | t0001 | g0276 | SAS | BEB | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| HG03834 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | BEB | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| HG03834 | hp2 | a0001 | c0001 | t0001 | g0264 | SAS | BEB | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| HG03927 | hp1 | a0001 | c0002 | t0001 | g0159 | SAS | BEB | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| HG03927 | hp2 | a0001 | c0001 | t0001 | g0239 | SAS | BEB | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| HG03942 | hp1 | a0001 | c0001 | t0002 | g0089 | SAS | BEB | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| HG04115 | hp1 | a0001 | c0004 | t0001 | g0258 | SAS | STU | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| HG04184 | hp1 | a0001 | c0003 | t0001 | g0174 | SAS | BEB | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| HG04184 | hp2 | a0001 | c0001 | t0001 | g0047 | SAS | BEB | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| HG04199 | hp1 | a0001 | c0002 | t0001 | g0004 | SAS | STU | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| HG04204 | hp1 | a0001 | c0002 | t0001 | g0177 | SAS | STU | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| HG04228 | hp1 | a0001 | c0002 | t0001 | g0037 | SAS | STU | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| NA18522 | hp1 | a0001 | c0002 | t0001 | g0134 | AFR | YRI | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| NA18612 | hp1 | a0001 | c0001 | t0002 | g0103 | EAS | CHB | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| NA18747 | hp1 | a0001 | c0001 | t0001 | g0203 | EAS | CHB | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| NA18940 | hp1 | a0001 | c0001 | t0009 | g0208 | EAS | JPT | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| NA18941 | hp1 | a0001 | c0003 | t0002 | g0031 | EAS | JPT | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| NA18941 | hp2 | a0001 | c0002 | t0001 | g0145 | EAS | JPT | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| NA18943 | hp1 | a0001 | c0003 | t0002 | g0035 | EAS | JPT | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| NA18944 | hp1 | a0001 | c0002 | t0001 | g0040 | EAS | JPT | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| NA18945 | hp1 | a0001 | c0001 | t0002 | g0084 | EAS | JPT | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| NA18946 | hp1 | a0001 | c0001 | t0001 | g0260 | EAS | JPT | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| NA18946 | hp2 | a0001 | c0001 | t0002 | g0113 | EAS | JPT | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| NA18948 | hp1 | a0001 | c0002 | t0001 | g0169 | EAS | JPT | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| NA18950 | hp1 | a0001 | c0001 | t0002 | g0105 | EAS | JPT | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| NA18950 | hp2 | a0001 | c0004 | t0001 | g0153 | EAS | JPT | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| NA18951 | hp1 | a0001 | c0001 | t0001 | g0216 | EAS | JPT | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| NA18951 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| NA18952 | hp1 | a0001 | c0001 | t0002 | g0011 | EAS | JPT | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| NA18953 | hp1 | a0005 | c0010 | t0007 | g0176 | EAS | JPT | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| NA18954 | hp1 | a0001 | c0001 | t0002 | g0053 | EAS | JPT | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| NA18954 | hp2 | a0001 | c0001 | t0001 | g0217 | EAS | JPT | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| NA18956 | hp1 | a0001 | c0002 | t0001 | g0029 | EAS | JPT | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| NA18956 | hp2 | a0001 | c0001 | t0001 | g0209 | EAS | JPT | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| NA18957 | hp1 | a0001 | c0002 | t0001 | g0146 | EAS | JPT | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| NA18957 | hp2 | a0001 | c0004 | t0001 | g0056 | EAS | JPT | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| NA18959 | hp1 | a0001 | c0001 | t0002 | g0090 | EAS | JPT | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| NA18960 | hp1 | a0001 | c0002 | t0001 | g0009 | EAS | JPT | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| NA18961 | hp1 | a0001 | c0001 | t0001 | g0026 | EAS | JPT | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| NA18962 | hp1 | a0001 | c0001 | t0002 | g0198 | EAS | JPT | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| NA18963 | hp1 | a0001 | c0001 | t0001 | g0275 | EAS | JPT | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| NA18963 | hp2 | a0001 | c0001 | t0002 | g0073 | EAS | JPT | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| NA18964 | hp1 | a0001 | c0001 | t0001 | g0234 | EAS | JPT | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| NA18964 | hp2 | a0001 | c0001 | t0001 | g0227 | EAS | JPT | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| NA18965 | hp1 | a0001 | c0001 | t0002 | g0091 | EAS | JPT | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| NA18967 | hp1 | a0001 | c0002 | t0001 | g0009 | EAS | JPT | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| NA18968 | hp1 | a0001 | c0004 | t0001 | g0201 | EAS | JPT | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| NA18968 | hp2 | a0001 | c0001 | t0002 | g0087 | EAS | JPT | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| NA18970 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| NA18971 | hp1 | a0001 | c0001 | t0001 | g0226 | EAS | JPT | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| NA18972 | hp1 | a0001 | c0001 | t0002 | g0079 | EAS | JPT | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| NA18972 | hp2 | a0006 | c0012 | t0001 | g0033 | EAS | JPT | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| NA18973 | hp1 | a0001 | c0002 | t0001 | g0142 | EAS | JPT | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| NA18973 | hp2 | a0001 | c0001 | t0002 | g0072 | EAS | JPT | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| NA18975 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| NA18975 | hp2 | a0001 | c0001 | t0002 | g0054 | EAS | JPT | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| NA18977 | hp1 | a0001 | c0001 | t0001 | g0218 | EAS | JPT | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| NA18982 | hp1 | a0001 | c0001 | t0002 | g0071 | EAS | JPT | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| NA18983 | hp1 | a0001 | c0001 | t0001 | g0215 | EAS | JPT | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| NA18984 | hp1 | a0001 | c0001 | t0002 | g0055 | EAS | JPT | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| NA18986 | hp1 | a0001 | c0002 | t0001 | g0032 | EAS | JPT | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| NA18988 | hp1 | a0001 | c0001 | t0001 | g0219 | EAS | JPT | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| NA18989 | hp1 | a0001 | c0001 | t0002 | g0016 | EAS | JPT | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| NA18990 | hp1 | a0001 | c0001 | t0001 | g0206 | EAS | JPT | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| NA18991 | hp1 | a0001 | c0001 | t0002 | g0115 | EAS | JPT | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| NA18991 | hp2 | a0001 | c0002 | t0001 | g0038 | EAS | JPT | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| NA18992 | hp1 | a0001 | c0001 | t0002 | g0106 | EAS | JPT | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| NA18992 | hp2 | a0001 | c0001 | t0001 | g0229 | EAS | JPT | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| NA18994 | hp1 | a0001 | c0001 | t0001 | g0261 | EAS | JPT | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| NA18995 | hp1 | a0001 | c0001 | t0002 | g0074 | EAS | JPT | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| NA18997 | hp1 | a0001 | c0003 | t0002 | g0066 | EAS | JPT | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| NA18997 | hp2 | a0001 | c0002 | t0001 | g0170 | EAS | JPT | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| NA18998 | hp1 | a0001 | c0002 | t0001 | g0148 | EAS | JPT | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| NA18998 | hp2 | a0001 | c0001 | t0002 | g0011 | EAS | JPT | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| NA19000 | hp1 | a0001 | c0002 | t0001 | g0131 | EAS | JPT | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| NA19002 | hp1 | a0001 | c0001 | t0001 | g0030 | EAS | JPT | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| NA19002 | hp2 | a0001 | c0001 | t0002 | g0092 | EAS | JPT | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| NA19003 | hp1 | a0001 | c0002 | t0001 | g0173 | EAS | JPT | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| NA19003 | hp2 | a0001 | c0001 | t0001 | g0247 | EAS | JPT | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| NA19004 | hp1 | a0001 | c0001 | t0001 | g0236 | EAS | JPT | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| NA19005 | hp1 | a0001 | c0001 | t0002 | g0085 | EAS | JPT | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| NA19006 | hp1 | a0001 | c0001 | t0001 | g0207 | EAS | JPT | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| NA19007 | hp1 | a0001 | c0004 | t0001 | g0253 | EAS | JPT | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| NA19009 | hp1 | a0001 | c0001 | t0002 | g0010 | EAS | JPT | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| NA19010 | hp1 | a0001 | c0009 | t0002 | g0093 | EAS | JPT | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| NA19010 | hp2 | a0001 | c0002 | t0001 | g0003 | EAS | JPT | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| NA19011 | hp1 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| NA19011 | hp2 | a0001 | c0001 | t0002 | g0075 | EAS | JPT | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| NA19012 | hp1 | a0001 | c0001 | t0001 | g0232 | EAS | JPT | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| NA19030 | hp1 | a0001 | c0002 | t0001 | g0162 | AFR | LWK | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| NA19030 | hp2 | a0001 | c0011 | t0003 | g0199 | AFR | LWK | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| NA19043 | hp1 | a0001 | c0002 | t0001 | g0164 | AFR | LWK | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| NA19055 | hp1 | a0001 | c0001 | t0001 | g0202 | EAS | JPT | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| NA19056 | hp1 | a0001 | c0001 | t0002 | g0065 | EAS | JPT | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| NA19057 | hp1 | a0001 | c0004 | t0001 | g0200 | EAS | JPT | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| NA19057 | hp2 | a0001 | c0001 | t0001 | g0270 | EAS | JPT | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| NA19058 | hp1 | a0001 | c0003 | t0002 | g0001 | EAS | JPT | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| NA19060 | hp1 | a0001 | c0001 | t0001 | g0233 | EAS | JPT | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| NA19062 | hp1 | a0001 | c0001 | t0002 | g0108 | EAS | JPT | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| NA19063 | hp1 | a0001 | c0002 | t0001 | g0048 | EAS | JPT | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| NA19064 | hp1 | a0001 | c0001 | t0001 | g0213 | EAS | JPT | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| NA19064 | hp2 | a0001 | c0001 | t0002 | g0069 | EAS | JPT | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| NA19065 | hp1 | a0001 | c0001 | t0001 | g0228 | EAS | JPT | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| NA19065 | hp2 | a0001 | c0001 | t0002 | g0012 | EAS | JPT | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| NA19066 | hp1 | a0001 | c0003 | t0002 | g0013 | EAS | JPT | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| NA19067 | hp1 | a0001 | c0001 | t0002 | g0067 | EAS | JPT | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| NA19068 | hp1 | a0001 | c0001 | t0001 | g0214 | EAS | JPT | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| NA19070 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| NA19072 | hp1 | a0001 | c0002 | t0001 | g0039 | EAS | JPT | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| NA19074 | hp1 | a0001 | c0001 | t0002 | g0077 | EAS | JPT | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| NA19074 | hp2 | a0001 | c0002 | t0001 | g0003 | EAS | JPT | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| NA19075 | hp1 | a0001 | c0002 | t0001 | g0121 | EAS | JPT | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| NA19076 | hp1 | a0001 | c0001 | t0002 | g0060 | EAS | JPT | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| NA19079 | hp1 | a0001 | c0001 | t0002 | g0082 | EAS | JPT | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| NA19080 | hp1 | a0001 | c0001 | t0001 | g0237 | EAS | JPT | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| NA19080 | hp2 | a0001 | c0001 | t0002 | g0078 | EAS | JPT | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| NA19081 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| NA19081 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| NA19082 | hp1 | a0001 | c0001 | t0002 | g0061 | EAS | JPT | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| NA19083 | hp1 | a0004 | c0008 | t0001 | g0256 | EAS | JPT | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| NA19084 | hp1 | a0001 | c0001 | t0002 | g0063 | EAS | JPT | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| NA19084 | hp2 | a0001 | c0002 | t0001 | g0003 | EAS | JPT | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| NA19085 | hp1 | a0001 | c0001 | t0002 | g0114 | EAS | JPT | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| NA19086 | hp1 | a0001 | c0001 | t0001 | g0222 | EAS | JPT | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| NA19087 | hp1 | a0001 | c0001 | t0002 | g0010 | EAS | JPT | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| NA19087 | hp2 | a0001 | c0001 | t0001 | g0235 | EAS | JPT | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| NA19088 | hp1 | a0001 | c0001 | t0002 | g0062 | EAS | JPT | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| NA19090 | hp1 | a0001 | c0002 | t0001 | g0046 | EAS | JPT | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| NA19090 | hp2 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| NA19091 | hp1 | a0001 | c0001 | t0001 | g0210 | EAS | JPT | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| NA19240 | hp1 | a0001 | c0002 | t0001 | g0136 | AFR | YRI | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| NA19240 | hp2 | a0001 | c0001 | t0001 | g0096 | AFR | YRI | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| NA20129 | hp1 | a0001 | c0002 | t0001 | g0119 | AFR | ASW | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| NA20129 | hp2 | a0001 | c0005 | t0001 | g0080 | AFR | ASW | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| NA20752 | hp1 | a0001 | c0001 | t0001 | g0249 | EUR | TSI | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| NA20805 | hp1 | a0001 | c0001 | t0001 | g0238 | EUR | TSI | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| NA20905 | hp1 | a0001 | c0001 | t0001 | g0240 | SAS | GIH | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| HG01123 | hp1 | a0001 | c0001 | t0001 | g0223 | AMR | CLM | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| HG01123 | hp2 | a0001 | c0001 | t0001 | g0262 | AMR | CLM | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| HG02109 | hp1 | a0001 | c0002 | t0001 | g0005 | AFR | ACB | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| HG02109 | hp2 | a0001 | c0002 | t0001 | g0166 | AFR | ACB | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| HG02486 | hp1 | a0001 | c0002 | t0001 | g0161 | AFR | ACB | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| HG02559 | hp1 | a0001 | c0004 | t0001 | g0278 | AFR | ACB | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| HG02559 | hp2 | a0001 | c0003 | t0001 | g0220 | AFR | ACB | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| HG03471 | hp1 | a0001 | c0004 | t0001 | g0279 | AFR | MSL | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| NA18955 | hp1 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0001 | g0274 | REF | REF | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| homoSapiens_grch38 | hp1 | a0001 | c0003 | t0001 | g0182 | REF | REF | LONRF3_chrX_118969618_119023355 | LONRF3 | chrX | 118969618 | 119023355 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chrX:118975145
|
C | G | 1 | a0002 | 4 | HG02451.hp2 HG02615.hp2 HG03041.hp2 others(1): Show |
missense_variant | MODERATE | c.365C>G | p.Ala122Gly | LONRF3 | ENSG00000175556.17 | transcript | ENST00000371628.8 | protein_coding | 1/11 | 528/3108 | 365/2280 | 122/759 | chrX | 118975145 | ||
| chrX:118989437
|
T | A | 1 | a0003 | 1 | HG01168.hp2 | missense_variant | MODERATE | c.1089T>A | p.Ser363Arg | LONRF3 | ENSG00000175556.17 | transcript | ENST00000371628.8 | protein_coding | 4/11 | 1252/3108 | 1089/2280 | 363/759 | chrX | 118989437 | ||
| chrX:118990510
|
A | AC | 1 | a0006 | 1 | NA18972.hp2 | frameshift_variant | HIGH | c.1367dupC | p.Leu457fs | LONRF3 | ENSG00000175556.17 | transcript | ENST00000371628.8 | protein_coding | 5/11 | 1531/3108 | 1368/2280 | 456/759 | INFO_REALIGN_3_PRIME | chrX | 118990510 | |
| chrX:119014238
|
G | GA | 1 | a0004 | 1 | NA19083.hp1 | frameshift_variant | HIGH | c.2007dupA | p.Leu670fs | LONRF3 | ENSG00000175556.17 | transcript | ENST00000371628.8 | protein_coding | 10/11 | 2171/3108 | 2008/2280 | 670/759 | INFO_REALIGN_3_PRIME | chrX | 119014238 | |
| chrX:119017604
|
CT | C | 1 | a0005 | 1 | NA18953.hp1 | frameshift_variant | HIGH | c.2195delT | p.Leu732fs | LONRF3 | ENSG00000175556.17 | transcript | ENST00000371628.8 | protein_coding | 11/11 | 2358/3108 | 2195/2280 | 732/759 | chrX | 119017604 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chrX:118974822
|
T | C | 6 | a0001c0001a0001c0004a0001c0005others(3): Show | 173 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(170): Show |
synonymous_variant | LOW | c.42T>C | p.Ala14Ala | LONRF3 | ENSG00000175556.17 | transcript | ENST00000371628.8 | protein_coding | 1/11 | 205/3108 | 42/2280 | 14/759 | chrX | 118974822 | ||
| chrX:118989647
|
G | T | 1 | a0001c0009 | 1 | NA19010.hp1 | synonymous_variant | LOW | c.1299G>T | p.Gly433Gly | LONRF3 | ENSG00000175556.17 | transcript | ENST00000371628.8 | protein_coding | 4/11 | 1462/3108 | 1299/2280 | 433/759 | chrX | 118989647 | ||
| chrX:119009146
|
C | T | 2 | a0001c0005a0001c0011 | 8 | HG00639.hp1 HG01884.hp2 HG02572.hp1 others(5): Show |
synonymous_variant | LOW | c.1551C>T | p.Tyr517Tyr | LONRF3 | ENSG00000175556.17 | transcript | ENST00000371628.8 | protein_coding | 7/11 | 1714/3108 | 1551/2280 | 517/759 | chrX | 119009146 | ||
| chrX:119014257
|
T | C | 1 | a0001c0009 | 1 | NA19010.hp1 | synonymous_variant | LOW | c.2025T>C | p.Tyr675Tyr | LONRF3 | ENSG00000175556.17 | transcript | ENST00000371628.8 | protein_coding | 10/11 | 2188/3108 | 2025/2280 | 675/759 | chrX | 119014257 | ||
| chrX:119014266
|
A | G | 5 | a0001c0002a0001c0004a0002c0006others(2): Show | 130 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(127): Show |
synonymous_variant | LOW | c.2034A>G | p.Ala678Ala | LONRF3 | ENSG00000175556.17 | transcript | ENST00000371628.8 | protein_coding | 10/11 | 2197/3108 | 2034/2280 | 678/759 | chrX | 119014266 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chrX:118974657
|
G | T | 1 | a0001c0001t0009 | 1 | NA18940.hp1 | 5_prime_UTR_variant | MODIFIER | c.-124G>T | LONRF3 | ENSG00000175556.17 | transcript | ENST00000371628.8 | protein_coding | 1/11 | 124 | chrX | 118974657 | |||||
| chrX:118974756
|
C | A | 1 | a0001c0002t0005 | 1 | HG02809.hp1 | 5_prime_UTR_variant | MODIFIER | c.-25C>A | LONRF3 | ENSG00000175556.17 | transcript | ENST00000371628.8 | protein_coding | 1/11 | 25 | chrX | 118974756 | |||||
| chrX:118974766
|
C | T | 3 | a0001c0002t0003a0001c0002t0008a0001c0011t0003 | 5 | HG02622.hp1 HG02723.hp1 HG02818.hp1 others(2): Show |
5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-15C>T | LONRF3 | ENSG00000175556.17 | transcript | ENST00000371628.8 | protein_coding | 1/11 | chrX | 118974766 | ||||||
| chrX:119017735
|
CG | C | 1 | a0001c0002t0005 | 1 | HG02809.hp1 | 3_prime_UTR_variant | MODIFIER | c.*51delG | LONRF3 | ENSG00000175556.17 | transcript | ENST00000371628.8 | protein_coding | 11/11 | 51 | INFO_REALIGN_3_PRIME | chrX | 119017735 | ||||
| chrX:119017849
|
CA | C | 1 | a0005c0010t0007 | 1 | NA18953.hp1 | 3_prime_UTR_variant | MODIFIER | c.*163delA | LONRF3 | ENSG00000175556.17 | transcript | ENST00000371628.8 | protein_coding | 11/11 | 163 | INFO_REALIGN_3_PRIME | chrX | 119017849 | ||||
| chrX:119017904
|
G | A | 2 | a0001c0002t0006a0001c0002t0008 | 2 | HG02630.hp1 HG02818.hp1 |
3_prime_UTR_variant | MODIFIER | c.*214G>A | LONRF3 | ENSG00000175556.17 | transcript | ENST00000371628.8 | protein_coding | 11/11 | 214 | chrX | 119017904 | |||||
| chrX:119017929
|
GT | G | 1 | a0005c0010t0007 | 1 | NA18953.hp1 | 3_prime_UTR_variant | MODIFIER | c.*242delT | LONRF3 | ENSG00000175556.17 | transcript | ENST00000371628.8 | protein_coding | 11/11 | 242 | INFO_REALIGN_3_PRIME | chrX | 119017929 | ||||
| chrX:119017967
|
TA | T | 1 | a0005c0010t0007 | 1 | NA18953.hp1 | 3_prime_UTR_variant | MODIFIER | c.*281delA | LONRF3 | ENSG00000175556.17 | transcript | ENST00000371628.8 | protein_coding | 11/11 | 281 | INFO_REALIGN_3_PRIME | chrX | 119017967 | ||||
| chrX:119017991
|
GT | G | 1 | a0005c0010t0007 | 1 | NA18953.hp1 | 3_prime_UTR_variant | MODIFIER | c.*305delT | LONRF3 | ENSG00000175556.17 | transcript | ENST00000371628.8 | protein_coding | 11/11 | 305 | INFO_REALIGN_3_PRIME | chrX | 119017991 | ||||
| chrX:119018225
|
G | A | 1 | a0001c0002t0004 | 2 | HG01891.hp1 HG03195.hp2 |
3_prime_UTR_variant | MODIFIER | c.*535G>A | LONRF3 | ENSG00000175556.17 | transcript | ENST00000371628.8 | protein_coding | 11/11 | 535 | chrX | 119018225 | |||||
| chrX:119018279
|
TA | T | 3 | a0001c0001t0002a0001c0003t0002a0001c0009t0002 | 64 | HG00099.hp2 HG00423.hp2 HG00438.hp2 others(61): Show |
3_prime_UTR_variant | MODIFIER | c.*590delA | LONRF3 | ENSG00000175556.17 | transcript | ENST00000371628.8 | protein_coding | 11/11 | 590 | chrX | 119018279 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chrX:118975668
|
C | G | 2 | a0001c0002t0004g0021a0001c0004t0001g0279 | 3 | HG01891.hp1 HG03195.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.817+71C>G | LONRF3 | ENSG00000175556.17 | transcript | ENST00000371628.8 | protein_coding | 1/10 | chrX | 118975668 | ||||||
| chrX:118975773
|
T | G | 1 | a0001c0002t0001g0022 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.817+176T>G | LONRF3 | ENSG00000175556.17 | transcript | ENST00000371628.8 | protein_coding | 1/10 | chrX | 118975773 | ||||||
| chrX:118975801
|
CTGTGTT | C | 1 | a0001c0002t0001g0023 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.817+211_817+216del others(6): Show |
LONRF3 | ENSG00000175556.17 | transcript | ENST00000371628.8 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chrX | 118975801 | |||||
| chrX:118975945
|
T | C | 1 | a0001c0004t0001g0279 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.817+348T>C | LONRF3 | ENSG00000175556.17 | transcript | ENST00000371628.8 | protein_coding | 1/10 | chrX | 118975945 | ||||||
| chrX:118975988
|
CCTT | C | 3 | a0001c0002t0001g0023a0001c0002t0001g0024a0001c0002t0003g0025 | 3 | HG01106.hp1 HG02886.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.817+394_817+396del others(3): Show |
LONRF3 | ENSG00000175556.17 | transcript | ENST00000371628.8 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chrX | 118975988 | |||||
| chrX:118976030
|
C | A | 2 | a0001c0001t0001g0026a0001c0001t0001g0027 | 2 | HG00597.hp1 NA18961.hp1 |
intron_variant | MODIFIER | c.817+433C>A | LONRF3 | ENSG00000175556.17 | transcript | ENST00000371628.8 | protein_coding | 1/10 | chrX | 118976030 | ||||||
| chrX:118976103
|
G | A | 1 | a0001c0002t0005g0028 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.817+506G>A | LONRF3 | ENSG00000175556.17 | transcript | ENST00000371628.8 | protein_coding | 1/10 | chrX | 118976103 | ||||||
| chrX:118976190
|
G | A | 20 | a0001c0001t0001g0030a0001c0002t0001g0008a0001c0002t0001g0009others(17): Show | 22 | HG00408.hp1 HG00423.hp1 HG00544.hp2 others(19): Show |
intron_variant | MODIFIER | c.817+593G>A | LONRF3 | ENSG00000175556.17 | transcript | ENST00000371628.8 | protein_coding | 1/10 | chrX | 118976190 | ||||||
| chrX:118976391
|
T | C | 1 | a0001c0002t0004g0021 | 2 | HG01891.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.817+794T>C | LONRF3 | ENSG00000175556.17 | transcript | ENST00000371628.8 | protein_coding | 1/10 | chrX | 118976391 | ||||||
| chrX:118976433
|
G | GC | 1 | a0001c0001t0001g0047 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.817+843dupC | LONRF3 | ENSG00000175556.17 | transcript | ENST00000371628.8 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chrX | 118976433 | |||||
| chrX:118976479
|
C | T | 1 | a0001c0004t0001g0278 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.817+882C>T | LONRF3 | ENSG00000175556.17 | transcript | ENST00000371628.8 | protein_coding | 1/10 | chrX | 118976479 | ||||||
| chrX:118976570
|
A | G | 1 | a0001c0004t0001g0277 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.817+973A>G | LONRF3 | ENSG00000175556.17 | transcript | ENST00000371628.8 | protein_coding | 1/10 | chrX | 118976570 | ||||||
| chrX:118976595
|
C | T | 21 | a0001c0001t0001g0030a0001c0002t0001g0008a0001c0002t0001g0009others(18): Show | 23 | HG00408.hp1 HG00423.hp1 HG00544.hp2 others(20): Show |
intron_variant | MODIFIER | c.817+998C>T | LONRF3 | ENSG00000175556.17 | transcript | ENST00000371628.8 | protein_coding | 1/10 | chrX | 118976595 | ||||||
| chrX:118976602
|
G | A | 2 | a0001c0002t0001g0024a0001c0002t0003g0025 | 2 | HG02886.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.817+1005G>A | LONRF3 | ENSG00000175556.17 | transcript | ENST00000371628.8 | protein_coding | 1/10 | chrX | 118976602 | ||||||
| chrX:118976738
|
C | T | 1 | a0001c0001t0001g0275 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.817+1141C>T | LONRF3 | ENSG00000175556.17 | transcript | ENST00000371628.8 | protein_coding | 1/10 | chrX | 118976738 | ||||||
| chrX:118976813
|
C | T | 1 | a0001c0004t0001g0278 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.817+1216C>T | LONRF3 | ENSG00000175556.17 | transcript | ENST00000371628.8 | protein_coding | 1/10 | chrX | 118976813 | ||||||
| chrX:118976814
|
G | A | 1 | a0001c0002t0005g0028 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.817+1217G>A | LONRF3 | ENSG00000175556.17 | transcript | ENST00000371628.8 | protein_coding | 1/10 | chrX | 118976814 | ||||||
| chrX:118976925
|
C | A | 1 | a0001c0002t0001g0048 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.817+1328C>A | LONRF3 | ENSG00000175556.17 | transcript | ENST00000371628.8 | protein_coding | 1/10 | chrX | 118976925 | ||||||
| chrX:118977058
|
C | T | 3 | a0001c0001t0001g0272a0001c0001t0001g0273a0001c0001t0001g0274 | 3 | HG01070.hp1 HG01071.hp1 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.818-1287C>T | LONRF3 | ENSG00000175556.17 | transcript | ENST00000371628.8 | protein_coding | 1/10 | chrX | 118977058 | ||||||
| chrX:118977085
|
A | G | 1 | a0001c0003t0002g0271 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.818-1260A>G | LONRF3 | ENSG00000175556.17 | transcript | ENST00000371628.8 | protein_coding | 1/10 | chrX | 118977085 | ||||||
| chrX:118977088
|
AAGAC | A | 4 | a0001c0002t0001g0023a0001c0002t0001g0024a0001c0002t0001g0049others(1): Show | 4 | HG01106.hp1 HG02717.hp1 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.818-1253_818-1250d others(6): Show |
LONRF3 | ENSG00000175556.17 | transcript | ENST00000371628.8 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chrX | 118977088 | |||||
| chrX:118977170
|
G | GA | 108 | a0001c0001t0001g0001a0001c0001t0001g0013a0001c0001t0001g0030others(105): Show | 117 | HG00099.hp2 HG00408.hp1 HG00408.hp2 others(114): Show |
intron_variant | MODIFIER | c.818-1165dupA | LONRF3 | ENSG00000175556.17 | transcript | ENST00000371628.8 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chrX | 118977170 | |||||
| chrX:118977170
|
G | GAA | 2 | a0001c0001t0002g0050a0001c0002t0001g0029 | 2 | HG00597.hp2 NA18956.hp1 |
intron_variant | MODIFIER | c.818-1166_818-1165d others(4): Show |
LONRF3 | ENSG00000175556.17 | transcript | ENST00000371628.8 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chrX | 118977170 | |||||
| chrX:118977273
|
T | C | 80 | a0001c0001t0001g0001a0001c0001t0001g0013a0001c0001t0001g0064others(77): Show | 87 | HG00099.hp2 HG00408.hp2 HG00423.hp2 others(84): Show |
intron_variant | MODIFIER | c.818-1072T>C | LONRF3 | ENSG00000175556.17 | transcript | ENST00000371628.8 | protein_coding | 1/10 | chrX | 118977273 | ||||||
| chrX:118977289
|
A | T | 3 | a0001c0001t0002g0113a0001c0001t0002g0114a0001c0001t0002g0115 | 3 | NA18946.hp2 NA18991.hp1 NA19085.hp1 |
intron_variant | MODIFIER | c.818-1056A>T | LONRF3 | ENSG00000175556.17 | transcript | ENST00000371628.8 | protein_coding | 1/10 | chrX | 118977289 | ||||||
| chrX:118977298
|
C | T | 3 | a0001c0001t0001g0268a0001c0001t0001g0269a0001c0001t0001g0270 | 3 | HG01934.hp1 HG02132.hp1 NA19057.hp2 |
intron_variant | MODIFIER | c.818-1047C>T | LONRF3 | ENSG00000175556.17 | transcript | ENST00000371628.8 | protein_coding | 1/10 | chrX | 118977298 | ||||||
| chrX:118977304
|
GC | G | 1 | a0001c0002t0001g0121 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.818-1039delC | LONRF3 | ENSG00000175556.17 | transcript | ENST00000371628.8 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chrX | 118977304 | |||||
| chrX:118977327
|
GC | G | 1 | a0001c0002t0001g0121 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.818-1014delC | LONRF3 | ENSG00000175556.17 | transcript | ENST00000371628.8 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chrX | 118977327 | |||||
| chrX:118977378
|
A | G | 26 | a0001c0002t0001g0008a0001c0002t0001g0009a0001c0002t0001g0023others(23): Show | 28 | HG00408.hp1 HG00423.hp1 HG00544.hp2 others(25): Show |
intron_variant | MODIFIER | c.818-967A>G | LONRF3 | ENSG00000175556.17 | transcript | ENST00000371628.8 | protein_coding | 1/10 | chrX | 118977378 | ||||||
| chrX:118977463
|
AG | A | 1 | a0001c0002t0001g0121 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.818-880delG | LONRF3 | ENSG00000175556.17 | transcript | ENST00000371628.8 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chrX | 118977463 | |||||
| chrX:118977499
|
AT | A | 1 | a0001c0002t0001g0121 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.818-844delT | LONRF3 | ENSG00000175556.17 | transcript | ENST00000371628.8 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chrX | 118977499 | |||||
| chrX:118977530
|
A | AC | 1 | a0001c0002t0001g0121 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.818-815_818-814ins others(1): Show |
LONRF3 | ENSG00000175556.17 | transcript | ENST00000371628.8 | protein_coding | 1/10 | chrX | 118977530 | ||||||
| chrX:118977676
|
C | T | 2 | a0001c0002t0001g0267a0001c0003t0001g0266 | 2 | HG00639.hp2 HG01517.hp1 |
intron_variant | MODIFIER | c.818-669C>T | LONRF3 | ENSG00000175556.17 | transcript | ENST00000371628.8 | protein_coding | 1/10 | chrX | 118977676 | ||||||
| chrX:118977739
|
C | T | 1 | a0001c0001t0001g0112 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.818-606C>T | LONRF3 | ENSG00000175556.17 | transcript | ENST00000371628.8 | protein_coding | 1/10 | chrX | 118977739 | ||||||
| chrX:118978031
|
A | G | 28 | a0001c0002t0001g0008a0001c0002t0001g0009a0001c0002t0001g0023others(25): Show | 31 | HG00408.hp1 HG00423.hp1 HG00544.hp2 others(28): Show |
intron_variant | MODIFIER | c.818-314A>G | LONRF3 | ENSG00000175556.17 | transcript | ENST00000371628.8 | protein_coding | 1/10 | chrX | 118978031 | ||||||
| chrX:118978121
|
G | A | 4 | a0001c0002t0001g0017a0001c0002t0001g0122a0001c0002t0001g0123others(1): Show | 5 | HG02055.hp1 HG02922.hp2 HG02976.hp2 others(2): Show |
intron_variant | MODIFIER | c.818-224G>A | LONRF3 | ENSG00000175556.17 | transcript | ENST00000371628.8 | protein_coding | 1/10 | chrX | 118978121 | ||||||
| chrX:118978219
|
C | T | 1 | a0001c0003t0001g0118 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.818-126C>T | LONRF3 | ENSG00000175556.17 | transcript | ENST00000371628.8 | protein_coding | 1/10 | chrX | 118978219 | ||||||
| chrX:118978511
|
T | A | 5 | a0001c0002t0001g0023a0001c0002t0001g0024a0001c0002t0001g0049others(2): Show | 6 | HG01106.hp1 HG01891.hp1 HG02717.hp1 others(3): Show |
intron_variant | MODIFIER | c.936+48T>A | LONRF3 | ENSG00000175556.17 | transcript | ENST00000371628.8 | protein_coding | 2/10 | chrX | 118978511 | ||||||
| chrX:118978737
|
G | C | 3 | a0001c0002t0001g0125a0001c0002t0001g0127a0001c0004t0001g0126 | 3 | HG00642.hp1 HG01192.hp1 HG01981.hp1 |
intron_variant | MODIFIER | c.936+274G>C | LONRF3 | ENSG00000175556.17 | transcript | ENST00000371628.8 | protein_coding | 2/10 | chrX | 118978737 | ||||||
| chrX:118978878
|
A | G | 1 | a0001c0002t0005g0028 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.936+415A>G | LONRF3 | ENSG00000175556.17 | transcript | ENST00000371628.8 | protein_coding | 2/10 | chrX | 118978878 | ||||||
| chrX:118978896
|
A | G | 208 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0006others(205): Show | 227 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(224): Show |
intron_variant | MODIFIER | c.936+433A>G | LONRF3 | ENSG00000175556.17 | transcript | ENST00000371628.8 | protein_coding | 2/10 | chrX | 118978896 | ||||||
| chrX:118978897
|
C | T | 82 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0007others(79): Show | 90 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(87): Show |
intron_variant | MODIFIER | c.936+434C>T | LONRF3 | ENSG00000175556.17 | transcript | ENST00000371628.8 | protein_coding | 2/10 | chrX | 118978897 | ||||||
| chrX:118978933
|
G | A | 2 | a0001c0001t0001g0026a0001c0001t0001g0027 | 2 | HG00597.hp1 NA18961.hp1 |
intron_variant | MODIFIER | c.936+470G>A | LONRF3 | ENSG00000175556.17 | transcript | ENST00000371628.8 | protein_coding | 2/10 | chrX | 118978933 | ||||||
| chrX:118978945
|
C | CCCTT | 8 | a0001c0002t0001g0128a0001c0002t0001g0185a0001c0002t0001g0189others(5): Show | 8 | HG01243.hp1 HG02622.hp1 HG02630.hp1 others(5): Show |
intron_variant | MODIFIER | c.936+503_936+506dup others(4): Show |
LONRF3 | ENSG00000175556.17 | transcript | ENST00000371628.8 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chrX | 118978945 | |||||
| chrX:118978945
|
C | CCCTTCCT others(1): Show |
1 | a0001c0004t0001g0279 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.936+499_936+506dup others(8): Show |
LONRF3 | ENSG00000175556.17 | transcript | ENST00000371628.8 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chrX | 118978945 | |||||
| chrX:118978945
|
CCCTT | C | 1 | a0001c0001t0001g0264 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.936+503_936+506del others(4): Show |
LONRF3 | ENSG00000175556.17 | transcript | ENST00000371628.8 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chrX | 118978945 | |||||
| chrX:118978969
|
TTC | T | 1 | a0001c0011t0003g0199 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.936+520_936+521del others(2): Show |
LONRF3 | ENSG00000175556.17 | transcript | ENST00000371628.8 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chrX | 118978969 | |||||
| chrX:118978998
|
C | CT | 4 | a0001c0001t0001g0263a0001c0002t0001g0024a0001c0002t0003g0025others(1): Show | 5 | HG01891.hp1 HG02886.hp1 HG03195.hp2 others(2): Show |
intron_variant | MODIFIER | c.936+555dupT | LONRF3 | ENSG00000175556.17 | transcript | ENST00000371628.8 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chrX | 118978998 | |||||
| chrX:118978998
|
CT | C | 203 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0006others(200): Show | 225 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(222): Show |
intron_variant | MODIFIER | c.936+555delT | LONRF3 | ENSG00000175556.17 | transcript | ENST00000371628.8 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chrX | 118978998 | |||||
| chrX:118978998
|
CTT | C | 26 | a0001c0001t0001g0026a0001c0001t0002g0053a0001c0001t0002g0054others(23): Show | 28 | HG00408.hp1 HG00423.hp1 HG00544.hp2 others(25): Show |
intron_variant | MODIFIER | c.936+554_936+555del others(2): Show |
LONRF3 | ENSG00000175556.17 | transcript | ENST00000371628.8 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chrX | 118978998 | |||||
| chrX:118978998
|
CTTT | C | 2 | a0001c0002t0001g0032a0001c0003t0002g0031 | 2 | NA18941.hp1 NA18986.hp1 |
intron_variant | MODIFIER | c.936+553_936+555del others(3): Show |
LONRF3 | ENSG00000175556.17 | transcript | ENST00000371628.8 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chrX | 118978998 | |||||
| chrX:118979003
|
T | C | 1 | a0001c0001t0002g0052 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.936+540T>C | LONRF3 | ENSG00000175556.17 | transcript | ENST00000371628.8 | protein_coding | 2/10 | chrX | 118979003 | ||||||
| chrX:118979069
|
C | T | 22 | a0001c0002t0001g0008a0001c0002t0001g0009a0001c0002t0001g0029others(19): Show | 24 | HG00408.hp1 HG00423.hp1 HG00544.hp2 others(21): Show |
intron_variant | MODIFIER | c.936+606C>T | LONRF3 | ENSG00000175556.17 | transcript | ENST00000371628.8 | protein_coding | 2/10 | chrX | 118979069 | ||||||
| chrX:118979101
|
C | T | 2 | a0001c0002t0001g0023a0001c0002t0001g0049 | 2 | HG01106.hp1 HG02717.hp1 |
intron_variant | MODIFIER | c.936+638C>T | LONRF3 | ENSG00000175556.17 | transcript | ENST00000371628.8 | protein_coding | 2/10 | chrX | 118979101 | ||||||
| chrX:118979176
|
A | AT | 2 | a0001c0001t0001g0026a0001c0001t0002g0103 | 2 | NA18612.hp1 NA18961.hp1 |
intron_variant | MODIFIER | c.936+722dupT | LONRF3 | ENSG00000175556.17 | transcript | ENST00000371628.8 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chrX | 118979176 | |||||
| chrX:118979177
|
T | C | 1 | a0001c0002t0001g0173 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.936+714T>C | LONRF3 | ENSG00000175556.17 | transcript | ENST00000371628.8 | protein_coding | 2/10 | chrX | 118979177 | ||||||
| chrX:118979211
|
G | A | 8 | a0001c0002t0001g0185a0001c0002t0001g0189a0001c0002t0003g0187others(5): Show | 8 | HG01243.hp1 HG02622.hp1 HG02630.hp1 others(5): Show |
intron_variant | MODIFIER | c.936+748G>A | LONRF3 | ENSG00000175556.17 | transcript | ENST00000371628.8 | protein_coding | 2/10 | chrX | 118979211 | ||||||
| chrX:118979245
|
C | T | 1 | a0001c0002t0001g0172 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.936+782C>T | LONRF3 | ENSG00000175556.17 | transcript | ENST00000371628.8 | protein_coding | 2/10 | chrX | 118979245 | ||||||
| chrX:118979282
|
C | A | 22 | a0001c0002t0001g0008a0001c0002t0001g0009a0001c0002t0001g0029others(19): Show | 24 | HG00408.hp1 HG00423.hp1 HG00544.hp2 others(21): Show |
intron_variant | MODIFIER | c.936+819C>A | LONRF3 | ENSG00000175556.17 | transcript | ENST00000371628.8 | protein_coding | 2/10 | chrX | 118979282 | ||||||
| chrX:118979282
|
C | T | 5 | a0001c0002t0001g0023a0001c0002t0001g0024a0001c0002t0001g0049others(2): Show | 6 | HG01106.hp1 HG01891.hp1 HG02717.hp1 others(3): Show |
intron_variant | MODIFIER | c.936+819C>T | LONRF3 | ENSG00000175556.17 | transcript | ENST00000371628.8 | protein_coding | 2/10 | chrX | 118979282 | ||||||
| chrX:118979300
|
C | CT | 1 | a0001c0002t0001g0121 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.936+848dupT | LONRF3 | ENSG00000175556.17 | transcript | ENST00000371628.8 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chrX | 118979300 | |||||
| chrX:118979300
|
C | CTTTTTTT others(2): Show |
1 | a0001c0002t0001g0049 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.936+840_936+848dup others(9): Show |
LONRF3 | ENSG00000175556.17 | transcript | ENST00000371628.8 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chrX | 118979300 | |||||
| chrX:118979300
|
C | CTTTTTTT others(3): Show |
3 | a0001c0002t0001g0023a0001c0002t0001g0024a0001c0002t0004g0021 | 4 | HG01106.hp1 HG01891.hp1 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.936+839_936+848dup others(10): Show |
LONRF3 | ENSG00000175556.17 | transcript | ENST00000371628.8 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chrX | 118979300 | |||||
| chrX:118979300
|
C | CTTTTTTT others(4): Show |
17 | a0001c0002t0001g0008a0001c0002t0001g0009a0001c0002t0001g0032others(14): Show | 19 | HG00408.hp1 HG00544.hp2 HG02027.hp1 others(16): Show |
intron_variant | MODIFIER | c.936+838_936+848dup others(11): Show |
LONRF3 | ENSG00000175556.17 | transcript | ENST00000371628.8 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chrX | 118979300 | |||||
| chrX:118979300
|
C | CTTTTTTT others(5): Show |
5 | a0001c0002t0001g0029a0001c0002t0001g0043a0001c0002t0001g0044others(2): Show | 5 | HG00423.hp1 HG02071.hp1 HG03209.hp1 others(2): Show |
intron_variant | MODIFIER | c.936+848_936+849ins others(12): Show |
LONRF3 | ENSG00000175556.17 | transcript | ENST00000371628.8 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chrX | 118979300 | |||||
| chrX:118979300
|
C | CTTTTTTT others(6): Show |
1 | a0001c0002t0001g0120 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.936+848_936+849ins others(13): Show |
LONRF3 | ENSG00000175556.17 | transcript | ENST00000371628.8 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chrX | 118979300 | |||||
| chrX:118979355
|
G | A | 1 | a0001c0004t0001g0192 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.936+892G>A | LONRF3 | ENSG00000175556.17 | transcript | ENST00000371628.8 | protein_coding | 2/10 | chrX | 118979355 | ||||||
| chrX:118979361
|
T | G | 22 | a0001c0002t0001g0008a0001c0002t0001g0009a0001c0002t0001g0029others(19): Show | 24 | HG00408.hp1 HG00423.hp1 HG00544.hp2 others(21): Show |
intron_variant | MODIFIER | c.936+898T>G | LONRF3 | ENSG00000175556.17 | transcript | ENST00000371628.8 | protein_coding | 2/10 | chrX | 118979361 | ||||||
| chrX:118979454
|
C | T | 1 | a0001c0001t0001g0239 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.936+991C>T | LONRF3 | ENSG00000175556.17 | transcript | ENST00000371628.8 | protein_coding | 2/10 | chrX | 118979454 | ||||||
| chrX:118979487
|
G | A | 75 | a0001c0001t0001g0001a0001c0001t0001g0013a0001c0001t0001g0064others(72): Show | 82 | HG00408.hp2 HG00423.hp2 HG00438.hp2 others(79): Show |
intron_variant | MODIFIER | c.936+1024G>A | LONRF3 | ENSG00000175556.17 | transcript | ENST00000371628.8 | protein_coding | 2/10 | chrX | 118979487 | ||||||
| chrX:118979509
|
C | CA | 1 | a0001c0001t0001g0026 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.936+1049dupA | LONRF3 | ENSG00000175556.17 | transcript | ENST00000371628.8 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chrX | 118979509 | |||||
| chrX:118979537
|
GC | G | 97 | a0001c0001t0001g0001a0001c0001t0001g0013a0001c0001t0001g0064others(94): Show | 106 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(103): Show |
intron_variant | MODIFIER | c.936+1076delC | LONRF3 | ENSG00000175556.17 | transcript | ENST00000371628.8 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chrX | 118979537 | |||||
| chrX:118979638
|
G | A | 2 | a0001c0001t0002g0057a0001c0001t0002g0104 | 2 | HG01928.hp1 HG01978.hp1 |
intron_variant | MODIFIER | c.936+1175G>A | LONRF3 | ENSG00000175556.17 | transcript | ENST00000371628.8 | protein_coding | 2/10 | chrX | 118979638 | ||||||
| chrX:118979797
|
TC | T | 1 | a0001c0001t0001g0026 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.936+1338delC | LONRF3 | ENSG00000175556.17 | transcript | ENST00000371628.8 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chrX | 118979797 | |||||
| chrX:118979818
|
TG | T | 1 | a0001c0001t0001g0026 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.936+1361delG | LONRF3 | ENSG00000175556.17 | transcript | ENST00000371628.8 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chrX | 118979818 | |||||
| chrX:118980019
|
GT | G | 1 | a0001c0001t0001g0026 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.936+1559delT | LONRF3 | ENSG00000175556.17 | transcript | ENST00000371628.8 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chrX | 118980019 | |||||
| chrX:118980125
|
C | T | 21 | a0001c0002t0001g0008a0001c0002t0001g0009a0001c0002t0001g0029others(18): Show | 23 | HG00408.hp1 HG00423.hp1 HG00544.hp2 others(20): Show |
intron_variant | MODIFIER | c.936+1662C>T | LONRF3 | ENSG00000175556.17 | transcript | ENST00000371628.8 | protein_coding | 2/10 | chrX | 118980125 | ||||||
| chrX:118980222
|
G | A | 177 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0007others(174): Show | 194 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(191): Show |
intron_variant | MODIFIER | c.936+1759G>A | LONRF3 | ENSG00000175556.17 | transcript | ENST00000371628.8 | protein_coding | 2/10 | chrX | 118980222 | ||||||
| chrX:118980230
|
A | G | 5 | a0001c0002t0001g0023a0001c0002t0001g0024a0001c0002t0001g0049others(2): Show | 6 | HG01106.hp1 HG01891.hp1 HG02717.hp1 others(3): Show |
intron_variant | MODIFIER | c.936+1767A>G | LONRF3 | ENSG00000175556.17 | transcript | ENST00000371628.8 | protein_coding | 2/10 | chrX | 118980230 | ||||||
| chrX:118980356
|
T | A | 172 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0007others(169): Show | 188 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(185): Show |
intron_variant | MODIFIER | c.936+1893T>A | LONRF3 | ENSG00000175556.17 | transcript | ENST00000371628.8 | protein_coding | 2/10 | chrX | 118980356 | ||||||
| chrX:118980366
|
AT | A | 1 | a0001c0005t0001g0058 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.936+1908delT | LONRF3 | ENSG00000175556.17 | transcript | ENST00000371628.8 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chrX | 118980366 | |||||
| chrX:118980373
|
A | T | 1 | a0001c0005t0001g0058 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.936+1910A>T | LONRF3 | ENSG00000175556.17 | transcript | ENST00000371628.8 | protein_coding | 2/10 | chrX | 118980373 | ||||||
| chrX:118980570
|
A | AT | 197 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0007others(194): Show | 216 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(213): Show |
intron_variant | MODIFIER | c.936+2116dupT | LONRF3 | ENSG00000175556.17 | transcript | ENST00000371628.8 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chrX | 118980570 | |||||
| chrX:118980570
|
A | ATT | 2 | a0001c0002t0001g0046a0002c0006t0001g0265 | 2 | HG03041.hp2 NA19090.hp1 |
intron_variant | MODIFIER | c.936+2115_936+2116d others(4): Show |
LONRF3 | ENSG00000175556.17 | transcript | ENST00000371628.8 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chrX | 118980570 | |||||
| chrX:118980632
|
A | G | 208 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0007others(205): Show | 227 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(224): Show |
intron_variant | MODIFIER | c.936+2169A>G | LONRF3 | ENSG00000175556.17 | transcript | ENST00000371628.8 | protein_coding | 2/10 | chrX | 118980632 | ||||||
| chrX:118980903
|
T | C | 6 | a0001c0002t0001g0023a0001c0002t0001g0024a0001c0002t0001g0043others(3): Show | 7 | HG01106.hp1 HG01891.hp1 HG02717.hp1 others(4): Show |
intron_variant | MODIFIER | c.937-1918T>C | LONRF3 | ENSG00000175556.17 | transcript | ENST00000371628.8 | protein_coding | 2/10 | chrX | 118980903 | ||||||
| chrX:118980923
|
A | G | 1 | a0001c0004t0001g0192 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.937-1898A>G | LONRF3 | ENSG00000175556.17 | transcript | ENST00000371628.8 | protein_coding | 2/10 | chrX | 118980923 | ||||||
| chrX:118981209
|
G | C | 1 | a0001c0004t0001g0201 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.937-1612G>C | LONRF3 | ENSG00000175556.17 | transcript | ENST00000371628.8 | protein_coding | 2/10 | chrX | 118981209 | ||||||
| chrX:118981336
|
T | A | 1 | a0001c0002t0001g0024 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.937-1485T>A | LONRF3 | ENSG00000175556.17 | transcript | ENST00000371628.8 | protein_coding | 2/10 | chrX | 118981336 | ||||||
| chrX:118981354
|
G | A | 1 | a0001c0004t0001g0129 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.937-1467G>A | LONRF3 | ENSG00000175556.17 | transcript | ENST00000371628.8 | protein_coding | 2/10 | chrX | 118981354 | ||||||
| chrX:118981365
|
G | T | 172 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0007others(169): Show | 188 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(185): Show |
intron_variant | MODIFIER | c.937-1456G>T | LONRF3 | ENSG00000175556.17 | transcript | ENST00000371628.8 | protein_coding | 2/10 | chrX | 118981365 | ||||||
| chrX:118981374
|
A | G | 68 | a0001c0001t0001g0152a0001c0002t0001g0003a0001c0002t0001g0004others(65): Show | 75 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(72): Show |
intron_variant | MODIFIER | c.937-1447A>G | LONRF3 | ENSG00000175556.17 | transcript | ENST00000371628.8 | protein_coding | 2/10 | chrX | 118981374 | ||||||
| chrX:118981416
|
T | C | 199 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0007others(196): Show | 218 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(215): Show |
intron_variant | MODIFIER | c.937-1405T>C | LONRF3 | ENSG00000175556.17 | transcript | ENST00000371628.8 | protein_coding | 2/10 | chrX | 118981416 | ||||||
| chrX:118981483
|
C | CA | 8 | a0001c0001t0002g0050a0001c0001t0002g0105a0001c0002t0001g0116others(5): Show | 8 | HG00597.hp2 HG01169.hp2 HG02145.hp1 others(5): Show |
intron_variant | MODIFIER | c.937-1322dupA | LONRF3 | ENSG00000175556.17 | transcript | ENST00000371628.8 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chrX | 118981483 | |||||
| chrX:118981483
|
C | CAA | 65 | a0001c0001t0001g0152a0001c0001t0001g0238a0001c0001t0001g0272others(62): Show | 71 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(68): Show |
intron_variant | MODIFIER | c.937-1323_937-1322d others(4): Show |
LONRF3 | ENSG00000175556.17 | transcript | ENST00000371628.8 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chrX | 118981483 | |||||
| chrX:118981483
|
C | CAAA | 108 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0007others(105): Show | 119 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(116): Show |
intron_variant | MODIFIER | c.937-1324_937-1322d others(5): Show |
LONRF3 | ENSG00000175556.17 | transcript | ENST00000371628.8 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chrX | 118981483 | |||||
| chrX:118981483
|
C | CAAAA | 1 | a0001c0001t0001g0202 | 1 | NA19055.hp1 | intron_variant | MODIFIER | c.937-1325_937-1322d others(6): Show |
LONRF3 | ENSG00000175556.17 | transcript | ENST00000371628.8 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chrX | 118981483 | |||||
| chrX:118981483
|
CA | C | 1 | a0001c0001t0002g0103 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.937-1322delA | LONRF3 | ENSG00000175556.17 | transcript | ENST00000371628.8 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chrX | 118981483 | |||||
| chrX:118982013
|
G | T | 2 | a0001c0002t0001g0195a0001c0002t0001g0196 | 2 | HG02970.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.937-808G>T | LONRF3 | ENSG00000175556.17 | transcript | ENST00000371628.8 | protein_coding | 2/10 | chrX | 118982013 | ||||||
| chrX:118982057
|
C | G | 1 | a0001c0002t0005g0028 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.937-764C>G | LONRF3 | ENSG00000175556.17 | transcript | ENST00000371628.8 | protein_coding | 2/10 | chrX | 118982057 | ||||||
| chrX:118982504
|
G | C | 1 | a0001c0001t0002g0050 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.937-317G>C | LONRF3 | ENSG00000175556.17 | transcript | ENST00000371628.8 | protein_coding | 2/10 | chrX | 118982504 | ||||||
| chrX:118982633
|
G | GT | 1 | a0001c0002t0001g0167 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.937-183dupT | LONRF3 | ENSG00000175556.17 | transcript | ENST00000371628.8 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chrX | 118982633 | |||||
| chrX:118982698
|
G | A | 1 | a0001c0004t0001g0279 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.937-123G>A | LONRF3 | ENSG00000175556.17 | transcript | ENST00000371628.8 | protein_coding | 2/10 | chrX | 118982698 | ||||||
| chrX:118982704
|
A | AAG | 1 | a0001c0002t0001g0132 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.937-112_937-111dup others(2): Show |
LONRF3 | ENSG00000175556.17 | transcript | ENST00000371628.8 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chrX | 118982704 | |||||
| chrX:118982773
|
G | A | 27 | a0001c0002t0001g0008a0001c0002t0001g0009a0001c0002t0001g0023others(24): Show | 30 | HG00408.hp1 HG00423.hp1 HG00544.hp2 others(27): Show |
intron_variant | MODIFIER | c.937-48G>A | LONRF3 | ENSG00000175556.17 | transcript | ENST00000371628.8 | protein_coding | 2/10 | chrX | 118982773 | ||||||
| chrX:118983090
|
G | A | 2 | a0001c0004t0001g0192a0001c0004t0001g0197 | 2 | HG02622.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.1059+147G>A | LONRF3 | ENSG00000175556.17 | transcript | ENST00000371628.8 | protein_coding | 3/10 | chrX | 118983090 | ||||||
| chrX:118983100
|
T | C | 56 | a0001c0001t0001g0152a0001c0002t0001g0003a0001c0002t0001g0004others(53): Show | 61 | HG00140.hp1 HG00323.hp1 HG00639.hp2 others(58): Show |
intron_variant | MODIFIER | c.1059+157T>C | LONRF3 | ENSG00000175556.17 | transcript | ENST00000371628.8 | protein_coding | 3/10 | chrX | 118983100 | ||||||
| chrX:118983627
|
C | T | 89 | a0001c0001t0001g0152a0001c0002t0001g0003a0001c0002t0001g0004others(86): Show | 98 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(95): Show |
intron_variant | MODIFIER | c.1059+684C>T | LONRF3 | ENSG00000175556.17 | transcript | ENST00000371628.8 | protein_coding | 3/10 | chrX | 118983627 | ||||||
| chrX:118983843
|
G | A | 3 | a0001c0002t0001g0024a0001c0002t0001g0043a0001c0002t0003g0025 | 3 | HG02886.hp1 HG03209.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.1059+900G>A | LONRF3 | ENSG00000175556.17 | transcript | ENST00000371628.8 | protein_coding | 3/10 | chrX | 118983843 | ||||||
| chrX:118983928
|
T | G | 10 | a0001c0002t0001g0185a0001c0002t0003g0187a0001c0002t0003g0188others(7): Show | 10 | HG01884.hp1 HG02622.hp1 HG02622.hp2 others(7): Show |
intron_variant | MODIFIER | c.1059+985T>G | LONRF3 | ENSG00000175556.17 | transcript | ENST00000371628.8 | protein_coding | 3/10 | chrX | 118983928 | ||||||
| chrX:118984069
|
G | C | 8 | a0001c0002t0001g0185a0001c0002t0003g0187a0001c0002t0003g0188others(5): Show | 8 | HG01884.hp1 HG02622.hp1 HG02630.hp1 others(5): Show |
intron_variant | MODIFIER | c.1059+1126G>C | LONRF3 | ENSG00000175556.17 | transcript | ENST00000371628.8 | protein_coding | 3/10 | chrX | 118984069 | ||||||
| chrX:118984714
|
T | C | 200 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0007others(197): Show | 219 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(216): Show |
intron_variant | MODIFIER | c.1059+1771T>C | LONRF3 | ENSG00000175556.17 | transcript | ENST00000371628.8 | protein_coding | 3/10 | chrX | 118984714 | ||||||
| chrX:118984722
|
C | T | 94 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0007others(91): Show | 103 | HG00280.hp1 HG00323.hp2 HG00438.hp1 others(100): Show |
intron_variant | MODIFIER | c.1059+1779C>T | LONRF3 | ENSG00000175556.17 | transcript | ENST00000371628.8 | protein_coding | 3/10 | chrX | 118984722 | ||||||
| chrX:118985115
|
C | G | 1 | a0001c0001t0001g0264 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.1059+2172C>G | LONRF3 | ENSG00000175556.17 | transcript | ENST00000371628.8 | protein_coding | 3/10 | chrX | 118985115 | ||||||
| chrX:118985509
|
C | A | 1 | a0001c0001t0001g0203 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.1059+2566C>A | LONRF3 | ENSG00000175556.17 | transcript | ENST00000371628.8 | protein_coding | 3/10 | chrX | 118985509 | ||||||
| chrX:118985714
|
T | C | 1 | a0001c0002t0001g0034 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.1059+2771T>C | LONRF3 | ENSG00000175556.17 | transcript | ENST00000371628.8 | protein_coding | 3/10 | chrX | 118985714 | ||||||
| chrX:118985739
|
A | G | 1 | a0001c0009t0002g0093 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.1059+2796A>G | LONRF3 | ENSG00000175556.17 | transcript | ENST00000371628.8 | protein_coding | 3/10 | chrX | 118985739 | ||||||
| chrX:118985798
|
TG | T | 1 | a0006c0012t0001g0033 | 1 | NA18972.hp2 | intron_variant | MODIFIER | c.1059+2857delG | LONRF3 | ENSG00000175556.17 | transcript | ENST00000371628.8 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chrX | 118985798 | |||||
| chrX:118986049
|
GA | G | 2 | a0001c0001t0002g0092a0001c0004t0001g0056 | 2 | NA18957.hp2 NA19002.hp2 |
intron_variant | MODIFIER | c.1059+3109delA | LONRF3 | ENSG00000175556.17 | transcript | ENST00000371628.8 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chrX | 118986049 | |||||
| chrX:118986050
|
AAAC | A | 1 | a0001c0001t0002g0091 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.1059+3109_1059+311 others(7): Show |
LONRF3 | ENSG00000175556.17 | transcript | ENST00000371628.8 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chrX | 118986050 | |||||
| chrX:118986050
|
AAACAC | A | 2 | a0001c0002t0001g0159a0001c0002t0001g0160 | 2 | HG03710.hp1 HG03927.hp1 |
intron_variant | MODIFIER | c.1059+3109_1059+311 others(9): Show |
LONRF3 | ENSG00000175556.17 | transcript | ENST00000371628.8 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chrX | 118986050 | |||||
| chrX:118986050
|
AAACACAC others(2): Show |
A | 2 | a0001c0001t0001g0237a0001c0001t0001g0261 | 2 | NA18994.hp1 NA19080.hp1 |
intron_variant | MODIFIER | c.1059+3109_1059+311 others(13): Show |
LONRF3 | ENSG00000175556.17 | transcript | ENST00000371628.8 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chrX | 118986050 | |||||
| chrX:118986050
|
AAACACAC others(4): Show |
A | 1 | a0001c0001t0001g0236 | 1 | NA19004.hp1 | intron_variant | MODIFIER | c.1059+3109_1059+311 others(15): Show |
LONRF3 | ENSG00000175556.17 | transcript | ENST00000371628.8 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chrX | 118986050 | |||||
| chrX:118986051
|
A | AAC | 4 | a0001c0001t0002g0087a0001c0001t0002g0088a0001c0001t0002g0089others(1): Show | 4 | HG00621.hp1 HG02258.hp1 HG03942.hp1 others(1): Show |
intron_variant | MODIFIER | c.1059+3158_1059+315 others(6): Show |
LONRF3 | ENSG00000175556.17 | transcript | ENST00000371628.8 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chrX | 118986051 | |||||
| chrX:118986051
|
A | AACAC | 3 | a0001c0001t0002g0090a0001c0001t0002g0198a0001c0004t0001g0099 | 3 | HG02922.hp1 NA18959.hp1 NA18962.hp1 |
intron_variant | MODIFIER | c.1059+3156_1059+315 others(8): Show |
LONRF3 | ENSG00000175556.17 | transcript | ENST00000371628.8 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chrX | 118986051 | |||||
| chrX:118986051
|
A | AC | 1 | a0001c0001t0001g0109 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.1059+3108_1059+310 others(5): Show |
LONRF3 | ENSG00000175556.17 | transcript | ENST00000371628.8 | protein_coding | 3/10 | chrX | 118986051 | ||||||
| chrX:118986051
|
AAC | A | 57 | a0001c0001t0001g0001a0001c0001t0001g0013a0001c0001t0001g0064others(54): Show | 66 | HG00099.hp2 HG00408.hp1 HG00408.hp2 others(63): Show |
intron_variant | MODIFIER | c.1059+3158_1059+315 others(6): Show |
LONRF3 | ENSG00000175556.17 | transcript | ENST00000371628.8 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chrX | 118986051 | |||||
| chrX:118986051
|
AACAC | A | 22 | a0001c0001t0002g0010a0001c0001t0002g0053a0001c0001t0002g0057others(19): Show | 24 | HG01069.hp1 HG01071.hp2 HG01099.hp1 others(21): Show |
intron_variant | MODIFIER | c.1059+3156_1059+315 others(8): Show |
LONRF3 | ENSG00000175556.17 | transcript | ENST00000371628.8 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chrX | 118986051 | |||||
| chrX:118986051
|
AACACAC | A | 15 | a0001c0001t0001g0096a0001c0001t0001g0152a0001c0001t0001g0259others(12): Show | 15 | HG00140.hp1 HG01106.hp1 HG01255.hp1 others(12): Show |
intron_variant | MODIFIER | c.1059+3154_1059+315 others(10): Show |
LONRF3 | ENSG00000175556.17 | transcript | ENST00000371628.8 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chrX | 118986051 | |||||
| chrX:118986051
|
AACACACA others(1): Show |
A | 59 | a0001c0001t0001g0203a0001c0001t0001g0226a0001c0001t0001g0227others(56): Show | 63 | HG00323.hp1 HG00639.hp2 HG00642.hp1 others(60): Show |
intron_variant | MODIFIER | c.1059+3152_1059+315 others(12): Show |
LONRF3 | ENSG00000175556.17 | transcript | ENST00000371628.8 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chrX | 118986051 | |||||
| chrX:118986051
|
AACACACA others(3): Show |
A | 75 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0007others(72): Show | 84 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(81): Show |
intron_variant | MODIFIER | c.1059+3150_1059+315 others(14): Show |
LONRF3 | ENSG00000175556.17 | transcript | ENST00000371628.8 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chrX | 118986051 | |||||
| chrX:118986051
|
AACACACA others(5): Show |
A | 5 | a0001c0001t0001g0270a0001c0001t0009g0208a0001c0002t0001g0133others(2): Show | 5 | HG00741.hp2 HG01109.hp1 NA18940.hp1 others(2): Show |
intron_variant | MODIFIER | c.1059+3148_1059+315 others(16): Show |
LONRF3 | ENSG00000175556.17 | transcript | ENST00000371628.8 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chrX | 118986051 | |||||
| chrX:118986051
|
AACACACA others(7): Show |
A | 13 | a0001c0001t0001g0206a0001c0001t0001g0207a0001c0001t0001g0268others(10): Show | 15 | HG01243.hp1 HG01934.hp1 HG02109.hp1 others(12): Show |
intron_variant | MODIFIER | c.1059+3146_1059+315 others(18): Show |
LONRF3 | ENSG00000175556.17 | transcript | ENST00000371628.8 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chrX | 118986051 | |||||
| chrX:118986051
|
AACACACA others(9): Show |
A | 3 | a0001c0001t0001g0112a0001c0001t0001g0204a0001c0001t0001g0205 | 3 | HG01257.hp2 HG01258.hp1 HG02896.hp1 |
intron_variant | MODIFIER | c.1059+3144_1059+315 others(20): Show |
LONRF3 | ENSG00000175556.17 | transcript | ENST00000371628.8 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chrX | 118986051 | |||||
| chrX:118986051
|
AACACACA others(11): Show |
A | 3 | a0001c0002t0001g0116a0001c0002t0001g0117a0001c0002t0005g0028 | 3 | HG02145.hp1 HG02809.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.1059+3142_1059+315 others(22): Show |
LONRF3 | ENSG00000175556.17 | transcript | ENST00000371628.8 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chrX | 118986051 | |||||
| chrX:118986091
|
CACACACA others(4): Show |
C | 1 | a0001c0001t0001g0235 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.1059+3150_1059+316 others(15): Show |
LONRF3 | ENSG00000175556.17 | transcript | ENST00000371628.8 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chrX | 118986091 | |||||
| chrX:118986529
|
A | G | 27 | a0001c0001t0001g0020a0001c0001t0001g0234a0001c0001t0001g0244others(24): Show | 28 | HG00323.hp2 HG00609.hp1 HG00738.hp1 others(25): Show |
intron_variant | MODIFIER | c.1060-2879A>G | LONRF3 | ENSG00000175556.17 | transcript | ENST00000371628.8 | protein_coding | 3/10 | chrX | 118986529 | ||||||
| chrX:118986622
|
G | A | 1 | a0001c0002t0001g0137 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.1060-2786G>A | LONRF3 | ENSG00000175556.17 | transcript | ENST00000371628.8 | protein_coding | 3/10 | chrX | 118986622 | ||||||
| chrX:118986681
|
C | T | 100 | a0001c0001t0001g0152a0001c0002t0001g0003a0001c0002t0001g0004others(97): Show | 109 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(106): Show |
intron_variant | MODIFIER | c.1060-2727C>T | LONRF3 | ENSG00000175556.17 | transcript | ENST00000371628.8 | protein_coding | 3/10 | chrX | 118986681 | ||||||
| chrX:118986686
|
C | T | 1 | a0001c0001t0001g0224 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.1060-2722C>T | LONRF3 | ENSG00000175556.17 | transcript | ENST00000371628.8 | protein_coding | 3/10 | chrX | 118986686 | ||||||
| chrX:118986843
|
T | TC | 1 | a0006c0012t0001g0033 | 1 | NA18972.hp2 | intron_variant | MODIFIER | c.1060-2562dupC | LONRF3 | ENSG00000175556.17 | transcript | ENST00000371628.8 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chrX | 118986843 | |||||
| chrX:118986956
|
CG | C | 1 | a0001c0001t0001g0026 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.1060-2447delG | LONRF3 | ENSG00000175556.17 | transcript | ENST00000371628.8 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chrX | 118986956 | |||||
| chrX:118986972
|
A | G | 1 | a0001c0001t0001g0233 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.1060-2436A>G | LONRF3 | ENSG00000175556.17 | transcript | ENST00000371628.8 | protein_coding | 3/10 | chrX | 118986972 | ||||||
| chrX:118986981
|
C | T | 1 | a0001c0004t0001g0278 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.1060-2427C>T | LONRF3 | ENSG00000175556.17 | transcript | ENST00000371628.8 | protein_coding | 3/10 | chrX | 118986981 | ||||||
| chrX:118987136
|
CA | C | 1 | a0001c0001t0001g0026 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.1060-2269delA | LONRF3 | ENSG00000175556.17 | transcript | ENST00000371628.8 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chrX | 118987136 | |||||
| chrX:118987153
|
C | A | 1 | a0001c0001t0001g0064 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.1060-2255C>A | LONRF3 | ENSG00000175556.17 | transcript | ENST00000371628.8 | protein_coding | 3/10 | chrX | 118987153 | ||||||
| chrX:118987240
|
A | AC | 1 | a0001c0001t0001g0026 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.1060-2167dupC | LONRF3 | ENSG00000175556.17 | transcript | ENST00000371628.8 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chrX | 118987240 | |||||
| chrX:118987283
|
G | A | 4 | a0001c0002t0001g0128a0001c0002t0001g0138a0001c0002t0001g0139others(1): Show | 4 | HG02109.hp2 HG02896.hp2 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.1060-2125G>A | LONRF3 | ENSG00000175556.17 | transcript | ENST00000371628.8 | protein_coding | 3/10 | chrX | 118987283 | ||||||
| chrX:118987295
|
T | C | 1 | a0001c0001t0001g0203 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.1060-2113T>C | LONRF3 | ENSG00000175556.17 | transcript | ENST00000371628.8 | protein_coding | 3/10 | chrX | 118987295 | ||||||
| chrX:118987386
|
T | TC | 1 | a0006c0012t0001g0033 | 1 | NA18972.hp2 | intron_variant | MODIFIER | c.1060-2019dupC | LONRF3 | ENSG00000175556.17 | transcript | ENST00000371628.8 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chrX | 118987386 | |||||
| chrX:118987419
|
A | T | 90 | a0001c0001t0001g0152a0001c0002t0001g0003a0001c0002t0001g0004others(87): Show | 99 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(96): Show |
intron_variant | MODIFIER | c.1060-1989A>T | LONRF3 | ENSG00000175556.17 | transcript | ENST00000371628.8 | protein_coding | 3/10 | chrX | 118987419 | ||||||
| chrX:118987424
|
C | T | 100 | a0001c0001t0001g0152a0001c0002t0001g0003a0001c0002t0001g0004others(97): Show | 109 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(106): Show |
intron_variant | MODIFIER | c.1060-1984C>T | LONRF3 | ENSG00000175556.17 | transcript | ENST00000371628.8 | protein_coding | 3/10 | chrX | 118987424 | ||||||
| chrX:118987444
|
A | AGTTTTT | 1 | a0001c0001t0001g0246 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.1060-1963_1060-195 others(10): Show |
LONRF3 | ENSG00000175556.17 | transcript | ENST00000371628.8 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chrX | 118987444 | |||||
| chrX:118987445
|
G | GT | 15 | a0001c0001t0001g0262a0001c0001t0002g0084a0001c0002t0001g0019others(12): Show | 15 | HG00741.hp1 HG01123.hp2 HG01884.hp1 others(12): Show |
intron_variant | MODIFIER | c.1060-1935dupT | LONRF3 | ENSG00000175556.17 | transcript | ENST00000371628.8 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chrX | 118987445 | |||||
| chrX:118987445
|
G | GTT | 69 | a0001c0001t0001g0152a0001c0002t0001g0003a0001c0002t0001g0004others(66): Show | 78 | HG00099.hp1 HG00140.hp1 HG00408.hp1 others(75): Show |
intron_variant | MODIFIER | c.1060-1936_1060-193 others(6): Show |
LONRF3 | ENSG00000175556.17 | transcript | ENST00000371628.8 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chrX | 118987445 | |||||
| chrX:118987445
|
G | GTTT | 14 | a0001c0001t0001g0202a0001c0002t0001g0044a0001c0002t0001g0045others(11): Show | 14 | HG00323.hp1 HG00423.hp1 HG02071.hp1 others(11): Show |
intron_variant | MODIFIER | c.1060-1937_1060-193 others(7): Show |
LONRF3 | ENSG00000175556.17 | transcript | ENST00000371628.8 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chrX | 118987445 | |||||
| chrX:118987445
|
G | GTTTT | 48 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0020others(45): Show | 54 | HG00544.hp1 HG01070.hp1 HG01071.hp1 others(51): Show |
intron_variant | MODIFIER | c.1060-1938_1060-193 others(8): Show |
LONRF3 | ENSG00000175556.17 | transcript | ENST00000371628.8 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chrX | 118987445 | |||||
| chrX:118987445
|
G | GTTTTT | 29 | a0001c0001t0001g0007a0001c0001t0001g0026a0001c0001t0001g0027others(26): Show | 31 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(28): Show |
intron_variant | MODIFIER | c.1060-1939_1060-193 others(9): Show |
LONRF3 | ENSG00000175556.17 | transcript | ENST00000371628.8 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chrX | 118987445 | |||||
| chrX:118987445
|
G | GTTTTTT | 8 | a0001c0001t0001g0111a0001c0001t0001g0204a0001c0001t0001g0205others(5): Show | 8 | HG00609.hp1 HG00733.hp1 HG01123.hp1 others(5): Show |
intron_variant | MODIFIER | c.1060-1940_1060-193 others(10): Show |
LONRF3 | ENSG00000175556.17 | transcript | ENST00000371628.8 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chrX | 118987445 | |||||
| chrX:118987445
|
G | GTTTTTTT | 8 | a0001c0001t0009g0208a0001c0002t0001g0017a0001c0002t0001g0122others(5): Show | 9 | HG02257.hp1 HG02895.hp1 HG02897.hp2 others(6): Show |
intron_variant | MODIFIER | c.1060-1941_1060-193 others(11): Show |
LONRF3 | ENSG00000175556.17 | transcript | ENST00000371628.8 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chrX | 118987445 | |||||
| chrX:118987445
|
G | GTTTTTTT others(1): Show |
2 | a0001c0002t0001g0123a0001c0003t0001g0194 | 2 | HG03453.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.1060-1942_1060-193 others(12): Show |
LONRF3 | ENSG00000175556.17 | transcript | ENST00000371628.8 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chrX | 118987445 | |||||
| chrX:118987445
|
G | GTTTTTTT others(2): Show |
1 | a0001c0002t0001g0124 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.1060-1943_1060-193 others(13): Show |
LONRF3 | ENSG00000175556.17 | transcript | ENST00000371628.8 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chrX | 118987445 | |||||
| chrX:118987445
|
GT | G | 51 | a0001c0001t0001g0001a0001c0001t0001g0013a0001c0001t0001g0064others(48): Show | 55 | HG00408.hp2 HG00423.hp2 HG00438.hp2 others(52): Show |
intron_variant | MODIFIER | c.1060-1935delT | LONRF3 | ENSG00000175556.17 | transcript | ENST00000371628.8 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chrX | 118987445 | |||||
| chrX:118987445
|
GTT | G | 4 | a0001c0001t0001g0107a0001c0003t0001g0094a0001c0003t0001g0097others(1): Show | 4 | HG01099.hp1 HG01167.hp1 HG01169.hp2 others(1): Show |
intron_variant | MODIFIER | c.1060-1936_1060-193 others(6): Show |
LONRF3 | ENSG00000175556.17 | transcript | ENST00000371628.8 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chrX | 118987445 | |||||
| chrX:118987445
|
GTTTTT | G | 1 | a0001c0002t0001g0161 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.1060-1939_1060-193 others(9): Show |
LONRF3 | ENSG00000175556.17 | transcript | ENST00000371628.8 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chrX | 118987445 | |||||
| chrX:118987446
|
T | TTTTTG | 2 | a0001c0001t0001g0244a0001c0001t0001g0245 | 2 | HG00738.hp1 HG01081.hp2 |
intron_variant | MODIFIER | c.1060-1958_1060-195 others(9): Show |
LONRF3 | ENSG00000175556.17 | transcript | ENST00000371628.8 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chrX | 118987446 | |||||
| chrX:118987447
|
T | TTTTTTG | 2 | a0001c0002t0001g0023a0001c0002t0003g0025 | 2 | HG01106.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.1060-1956_1060-195 others(10): Show |
LONRF3 | ENSG00000175556.17 | transcript | ENST00000371628.8 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chrX | 118987447 | |||||
| chrX:118987448
|
T | TTTTTG | 4 | a0001c0002t0001g0024a0001c0002t0001g0043a0001c0002t0001g0049others(1): Show | 5 | HG01891.hp1 HG02717.hp1 HG02886.hp1 others(2): Show |
intron_variant | MODIFIER | c.1060-1956_1060-195 others(9): Show |
LONRF3 | ENSG00000175556.17 | transcript | ENST00000371628.8 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chrX | 118987448 | |||||
| chrX:118987455
|
T | G | 1 | a0001c0002t0001g0049 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.1060-1953T>G | LONRF3 | ENSG00000175556.17 | transcript | ENST00000371628.8 | protein_coding | 3/10 | chrX | 118987455 | ||||||
| chrX:118987599
|
C | T | 4 | a0001c0002t0001g0024a0001c0002t0001g0154a0001c0002t0001g0156others(1): Show | 4 | HG02886.hp1 HG03017.hp1 HG03654.hp1 others(1): Show |
intron_variant | MODIFIER | c.1060-1809C>T | LONRF3 | ENSG00000175556.17 | transcript | ENST00000371628.8 | protein_coding | 3/10 | chrX | 118987599 | ||||||
| chrX:118987677
|
TG | T | 1 | a0006c0012t0001g0033 | 1 | NA18972.hp2 | intron_variant | MODIFIER | c.1060-1727delG | LONRF3 | ENSG00000175556.17 | transcript | ENST00000371628.8 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chrX | 118987677 | |||||
| chrX:118987829
|
T | C | 1 | a0003c0007t0001g0225 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.1060-1579T>C | LONRF3 | ENSG00000175556.17 | transcript | ENST00000371628.8 | protein_coding | 3/10 | chrX | 118987829 | ||||||
| chrX:118988028
|
A | G | 6 | a0001c0002t0001g0023a0001c0002t0001g0024a0001c0002t0001g0043others(3): Show | 7 | HG01106.hp1 HG01891.hp1 HG02717.hp1 others(4): Show |
intron_variant | MODIFIER | c.1060-1380A>G | LONRF3 | ENSG00000175556.17 | transcript | ENST00000371628.8 | protein_coding | 3/10 | chrX | 118988028 | ||||||
| chrX:118988032
|
C | T | 2 | a0001c0001t0002g0057a0001c0001t0002g0104 | 2 | HG01928.hp1 HG01978.hp1 |
intron_variant | MODIFIER | c.1060-1376C>T | LONRF3 | ENSG00000175556.17 | transcript | ENST00000371628.8 | protein_coding | 3/10 | chrX | 118988032 | ||||||
| chrX:118988056
|
C | T | 1 | a0001c0001t0001g0261 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.1060-1352C>T | LONRF3 | ENSG00000175556.17 | transcript | ENST00000371628.8 | protein_coding | 3/10 | chrX | 118988056 | ||||||
| chrX:118988101
|
GC | G | 1 | a0001c0001t0001g0222 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.1060-1304delC | LONRF3 | ENSG00000175556.17 | transcript | ENST00000371628.8 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chrX | 118988101 | |||||
| chrX:118988164
|
G | A | 10 | a0001c0002t0001g0185a0001c0002t0003g0187a0001c0002t0003g0188others(7): Show | 10 | HG01884.hp1 HG02622.hp1 HG02622.hp2 others(7): Show |
intron_variant | MODIFIER | c.1060-1244G>A | LONRF3 | ENSG00000175556.17 | transcript | ENST00000371628.8 | protein_coding | 3/10 | chrX | 118988164 | ||||||
| chrX:118988331
|
C | T | 208 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0007others(205): Show | 227 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(224): Show |
intron_variant | MODIFIER | c.1060-1077C>T | LONRF3 | ENSG00000175556.17 | transcript | ENST00000371628.8 | protein_coding | 3/10 | chrX | 118988331 | ||||||
| chrX:118988557
|
T | C | 106 | a0001c0001t0001g0152a0001c0002t0001g0003a0001c0002t0001g0004others(103): Show | 116 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(113): Show |
intron_variant | MODIFIER | c.1060-851T>C | LONRF3 | ENSG00000175556.17 | transcript | ENST00000371628.8 | protein_coding | 3/10 | chrX | 118988557 | ||||||
| chrX:118988729
|
T | G | 1 | a0001c0002t0001g0172 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.1060-679T>G | LONRF3 | ENSG00000175556.17 | transcript | ENST00000371628.8 | protein_coding | 3/10 | chrX | 118988729 | ||||||
| chrX:118988766
|
A | T | 1 | a0001c0002t0001g0044 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.1060-642A>T | LONRF3 | ENSG00000175556.17 | transcript | ENST00000371628.8 | protein_coding | 3/10 | chrX | 118988766 | ||||||
| chrX:118988799
|
CT | C | 55 | a0001c0001t0001g0020a0001c0001t0001g0204a0001c0001t0001g0234others(52): Show | 58 | HG00323.hp1 HG00323.hp2 HG00609.hp1 others(55): Show |
intron_variant | MODIFIER | c.1060-594delT | LONRF3 | ENSG00000175556.17 | transcript | ENST00000371628.8 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chrX | 118988799 | |||||
| chrX:118988799
|
CTT | C | 1 | a0001c0001t0002g0065 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.1060-595_1060-594d others(4): Show |
LONRF3 | ENSG00000175556.17 | transcript | ENST00000371628.8 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chrX | 118988799 | |||||
| chrX:118988832
|
A | AT | 1 | a0006c0012t0001g0033 | 1 | NA18972.hp2 | intron_variant | MODIFIER | c.1060-575dupT | LONRF3 | ENSG00000175556.17 | transcript | ENST00000371628.8 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chrX | 118988832 | |||||
| chrX:118988941
|
A | G | 2 | a0001c0001t0001g0255a0001c0001t0001g0257 | 2 | HG00609.hp1 HG02165.hp1 |
intron_variant | MODIFIER | c.1060-467A>G | LONRF3 | ENSG00000175556.17 | transcript | ENST00000371628.8 | protein_coding | 3/10 | chrX | 118988941 | ||||||
| chrX:118988969
|
G | GA | 1 | a0006c0012t0001g0033 | 1 | NA18972.hp2 | intron_variant | MODIFIER | c.1060-439_1060-438i others(3): Show |
LONRF3 | ENSG00000175556.17 | transcript | ENST00000371628.8 | protein_coding | 3/10 | chrX | 118988969 | ||||||
| chrX:118989009
|
G | GA | 1 | a0006c0012t0001g0033 | 1 | NA18972.hp2 | intron_variant | MODIFIER | c.1060-397dupA | LONRF3 | ENSG00000175556.17 | transcript | ENST00000371628.8 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chrX | 118989009 | |||||
| chrX:118989014
|
A | C | 1 | a0001c0003t0002g0271 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.1060-394A>C | LONRF3 | ENSG00000175556.17 | transcript | ENST00000371628.8 | protein_coding | 3/10 | chrX | 118989014 | ||||||
| chrX:118989031
|
GC | G | 1 | a0006c0012t0001g0033 | 1 | NA18972.hp2 | intron_variant | MODIFIER | c.1060-375delC | LONRF3 | ENSG00000175556.17 | transcript | ENST00000371628.8 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chrX | 118989031 | |||||
| chrX:118989097
|
T | TG | 1 | a0006c0012t0001g0033 | 1 | NA18972.hp2 | intron_variant | MODIFIER | c.1060-309dupG | LONRF3 | ENSG00000175556.17 | transcript | ENST00000371628.8 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chrX | 118989097 | |||||
| chrX:118989127
|
A | G | 90 | a0001c0001t0001g0152a0001c0002t0001g0003a0001c0002t0001g0004others(87): Show | 99 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(96): Show |
intron_variant | MODIFIER | c.1060-281A>G | LONRF3 | ENSG00000175556.17 | transcript | ENST00000371628.8 | protein_coding | 3/10 | chrX | 118989127 | ||||||
| chrX:118989158
|
AC | A | 1 | a0006c0012t0001g0033 | 1 | NA18972.hp2 | intron_variant | MODIFIER | c.1060-248delC | LONRF3 | ENSG00000175556.17 | transcript | ENST00000371628.8 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chrX | 118989158 | |||||
| chrX:118989201
|
G | T | 1 | a0001c0004t0001g0153 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.1060-207G>T | LONRF3 | ENSG00000175556.17 | transcript | ENST00000371628.8 | protein_coding | 3/10 | chrX | 118989201 | ||||||
| chrX:118989245
|
G | GA | 1 | a0006c0012t0001g0033 | 1 | NA18972.hp2 | intron_variant | MODIFIER | c.1060-160dupA | LONRF3 | ENSG00000175556.17 | transcript | ENST00000371628.8 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chrX | 118989245 | |||||
| chrX:118989711
|
A | G | 1 | a0001c0004t0001g0279 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1324+39A>G | LONRF3 | ENSG00000175556.17 | transcript | ENST00000371628.8 | protein_coding | 4/10 | chrX | 118989711 | ||||||
| chrX:118989712
|
TC | T | 1 | a0006c0012t0001g0033 | 1 | NA18972.hp2 | intron_variant | MODIFIER | c.1324+44delC | LONRF3 | ENSG00000175556.17 | transcript | ENST00000371628.8 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chrX | 118989712 | |||||
| chrX:118989753
|
TG | T | 1 | a0006c0012t0001g0033 | 1 | NA18972.hp2 | intron_variant | MODIFIER | c.1324+86delG | LONRF3 | ENSG00000175556.17 | transcript | ENST00000371628.8 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chrX | 118989753 | |||||
| chrX:118989802
|
G | T | 90 | a0001c0001t0001g0152a0001c0002t0001g0003a0001c0002t0001g0004others(87): Show | 99 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(96): Show |
intron_variant | MODIFIER | c.1324+130G>T | LONRF3 | ENSG00000175556.17 | transcript | ENST00000371628.8 | protein_coding | 4/10 | chrX | 118989802 | ||||||
| chrX:118989927
|
G | A | 1 | a0001c0001t0001g0247 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.1324+255G>A | LONRF3 | ENSG00000175556.17 | transcript | ENST00000371628.8 | protein_coding | 4/10 | chrX | 118989927 | ||||||
| chrX:118989976
|
G | A | 3 | a0001c0002t0001g0116a0001c0002t0001g0117a0001c0002t0005g0028 | 3 | HG02145.hp1 HG02809.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.1324+304G>A | LONRF3 | ENSG00000175556.17 | transcript | ENST00000371628.8 | protein_coding | 4/10 | chrX | 118989976 | ||||||
| chrX:118989990
|
A | AC | 2 | a0001c0001t0001g0107a0001c0001t0002g0115 | 2 | HG02280.hp2 NA18991.hp1 |
intron_variant | MODIFIER | c.1324+323dupC | LONRF3 | ENSG00000175556.17 | transcript | ENST00000371628.8 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chrX | 118989990 | |||||
| chrX:118990259
|
A | AT | 1 | a0006c0012t0001g0033 | 1 | NA18972.hp2 | intron_variant | MODIFIER | c.1325-208dupT | LONRF3 | ENSG00000175556.17 | transcript | ENST00000371628.8 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chrX | 118990259 | |||||
| chrX:118990277
|
C | G | 200 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0007others(197): Show | 219 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(216): Show |
intron_variant | MODIFIER | c.1325-193C>G | LONRF3 | ENSG00000175556.17 | transcript | ENST00000371628.8 | protein_coding | 4/10 | chrX | 118990277 | ||||||
| chrX:118990731
|
G | C | 90 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0007others(87): Show | 99 | HG00280.hp1 HG00323.hp2 HG00438.hp1 others(96): Show |
intron_variant | MODIFIER | c.1415+171G>C | LONRF3 | ENSG00000175556.17 | transcript | ENST00000371628.8 | protein_coding | 5/10 | chrX | 118990731 | ||||||
| chrX:118990866
|
CT | C | 1 | a0006c0012t0001g0033 | 1 | NA18972.hp2 | intron_variant | MODIFIER | c.1415+314delT | LONRF3 | ENSG00000175556.17 | transcript | ENST00000371628.8 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chrX | 118990866 | |||||
| chrX:118990967
|
C | G | 10 | a0001c0002t0001g0185a0001c0002t0003g0187a0001c0002t0003g0188others(7): Show | 10 | HG01884.hp1 HG02622.hp1 HG02622.hp2 others(7): Show |
intron_variant | MODIFIER | c.1415+407C>G | LONRF3 | ENSG00000175556.17 | transcript | ENST00000371628.8 | protein_coding | 5/10 | chrX | 118990967 | ||||||
| chrX:118990990
|
TG | T | 1 | a0006c0012t0001g0033 | 1 | NA18972.hp2 | intron_variant | MODIFIER | c.1415+433delG | LONRF3 | ENSG00000175556.17 | transcript | ENST00000371628.8 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chrX | 118990990 | |||||
| chrX:118991067
|
AG | A | 1 | a0006c0012t0001g0033 | 1 | NA18972.hp2 | intron_variant | MODIFIER | c.1415+509delG | LONRF3 | ENSG00000175556.17 | transcript | ENST00000371628.8 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chrX | 118991067 | |||||
| chrX:118991241
|
G | GC | 1 | a0001c0002t0001g0038 | 1 | NA18991.hp2 | intron_variant | MODIFIER | c.1415+686dupC | LONRF3 | ENSG00000175556.17 | transcript | ENST00000371628.8 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chrX | 118991241 | |||||
| chrX:118991255
|
C | A | 113 | a0001c0001t0001g0152a0001c0002t0001g0003a0001c0002t0001g0004others(110): Show | 123 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(120): Show |
intron_variant | MODIFIER | c.1415+695C>A | LONRF3 | ENSG00000175556.17 | transcript | ENST00000371628.8 | protein_coding | 5/10 | chrX | 118991255 | ||||||
| chrX:118991393
|
A | AT | 119 | a0001c0001t0001g0152a0001c0002t0001g0003a0001c0002t0001g0004others(116): Show | 130 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(127): Show |
intron_variant | MODIFIER | c.1415+833_1415+834i others(3): Show |
LONRF3 | ENSG00000175556.17 | transcript | ENST00000371628.8 | protein_coding | 5/10 | chrX | 118991393 | ||||||
| chrX:118991407
|
GC | G | 1 | a0006c0012t0001g0033 | 1 | NA18972.hp2 | intron_variant | MODIFIER | c.1415+849delC | LONRF3 | ENSG00000175556.17 | transcript | ENST00000371628.8 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chrX | 118991407 | |||||
| chrX:118991864
|
A | AT | 116 | a0001c0001t0001g0152a0001c0002t0001g0003a0001c0002t0001g0004others(113): Show | 127 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(124): Show |
intron_variant | MODIFIER | c.1415+1313dupT | LONRF3 | ENSG00000175556.17 | transcript | ENST00000371628.8 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chrX | 118991864 | |||||
| chrX:118991864
|
AT | A | 3 | a0001c0002t0001g0116a0001c0002t0001g0117a0001c0002t0005g0028 | 3 | HG02145.hp1 HG02809.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.1415+1313delT | LONRF3 | ENSG00000175556.17 | transcript | ENST00000371628.8 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chrX | 118991864 | |||||
| chrX:118992167
|
CA | C | 1 | a0006c0012t0001g0033 | 1 | NA18972.hp2 | intron_variant | MODIFIER | c.1415+1610delA | LONRF3 | ENSG00000175556.17 | transcript | ENST00000371628.8 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chrX | 118992167 | |||||
| chrX:118992185
|
AG | A | 1 | a0006c0012t0001g0033 | 1 | NA18972.hp2 | intron_variant | MODIFIER | c.1415+1628delG | LONRF3 | ENSG00000175556.17 | transcript | ENST00000371628.8 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chrX | 118992185 | |||||
| chrX:118992335
|
C | T | 25 | a0001c0002t0001g0008a0001c0002t0001g0009a0001c0002t0001g0019others(22): Show | 27 | HG00408.hp1 HG00423.hp1 HG00544.hp2 others(24): Show |
intron_variant | MODIFIER | c.1415+1775C>T | LONRF3 | ENSG00000175556.17 | transcript | ENST00000371628.8 | protein_coding | 5/10 | chrX | 118992335 | ||||||
| chrX:118992661
|
CT | C | 1 | a0006c0012t0001g0033 | 1 | NA18972.hp2 | intron_variant | MODIFIER | c.1415+2102delT | LONRF3 | ENSG00000175556.17 | transcript | ENST00000371628.8 | protein_coding | 5/10 | chrX | 118992661 | ||||||
| chrX:118992672
|
G | C | 1 | a0001c0001t0001g0107 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.1415+2112G>C | LONRF3 | ENSG00000175556.17 | transcript | ENST00000371628.8 | protein_coding | 5/10 | chrX | 118992672 | ||||||
| chrX:118992718
|
C | CA | 1 | a0006c0012t0001g0033 | 1 | NA18972.hp2 | intron_variant | MODIFIER | c.1415+2163dupA | LONRF3 | ENSG00000175556.17 | transcript | ENST00000371628.8 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chrX | 118992718 | |||||
| chrX:118992766
|
A | C | 1 | a0001c0003t0001g0174 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.1415+2206A>C | LONRF3 | ENSG00000175556.17 | transcript | ENST00000371628.8 | protein_coding | 5/10 | chrX | 118992766 | ||||||
| chrX:118992775
|
A | T | 116 | a0001c0001t0001g0152a0001c0002t0001g0003a0001c0002t0001g0004others(113): Show | 127 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(124): Show |
intron_variant | MODIFIER | c.1415+2215A>T | LONRF3 | ENSG00000175556.17 | transcript | ENST00000371628.8 | protein_coding | 5/10 | chrX | 118992775 | ||||||
| chrX:118992778
|
A | G | 116 | a0001c0001t0001g0152a0001c0002t0001g0003a0001c0002t0001g0004others(113): Show | 127 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(124): Show |
intron_variant | MODIFIER | c.1415+2218A>G | LONRF3 | ENSG00000175556.17 | transcript | ENST00000371628.8 | protein_coding | 5/10 | chrX | 118992778 | ||||||
| chrX:118992810
|
T | C | 106 | a0001c0001t0001g0152a0001c0002t0001g0003a0001c0002t0001g0004others(103): Show | 116 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(113): Show |
intron_variant | MODIFIER | c.1415+2250T>C | LONRF3 | ENSG00000175556.17 | transcript | ENST00000371628.8 | protein_coding | 5/10 | chrX | 118992810 | ||||||
| chrX:118992812
|
T | TA | 1 | a0006c0012t0001g0033 | 1 | NA18972.hp2 | intron_variant | MODIFIER | c.1415+2253dupA | LONRF3 | ENSG00000175556.17 | transcript | ENST00000371628.8 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chrX | 118992812 | |||||
| chrX:118993120
|
A | AC | 1 | a0001c0001t0001g0222 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.1415+2569dupC | LONRF3 | ENSG00000175556.17 | transcript | ENST00000371628.8 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chrX | 118993120 | |||||
| chrX:118993121
|
C | CCA | 115 | a0001c0001t0001g0152a0001c0002t0001g0003a0001c0002t0001g0004others(112): Show | 126 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(123): Show |
intron_variant | MODIFIER | c.1415+2562_1415+256 others(6): Show |
LONRF3 | ENSG00000175556.17 | transcript | ENST00000371628.8 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chrX | 118993121 | |||||
| chrX:118993126
|
C | T | 1 | a0001c0002t0001g0041 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.1415+2566C>T | LONRF3 | ENSG00000175556.17 | transcript | ENST00000371628.8 | protein_coding | 5/10 | chrX | 118993126 | ||||||
| chrX:118993127
|
C | A | 1 | a0001c0002t0006g0184 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.1415+2567C>A | LONRF3 | ENSG00000175556.17 | transcript | ENST00000371628.8 | protein_coding | 5/10 | chrX | 118993127 | ||||||
| chrX:118993128
|
C | G | 1 | a0001c0004t0001g0099 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.1415+2568C>G | LONRF3 | ENSG00000175556.17 | transcript | ENST00000371628.8 | protein_coding | 5/10 | chrX | 118993128 | ||||||
| chrX:118993129
|
C | A | 115 | a0001c0001t0001g0152a0001c0002t0001g0003a0001c0002t0001g0004others(112): Show | 126 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(123): Show |
intron_variant | MODIFIER | c.1415+2569C>A | LONRF3 | ENSG00000175556.17 | transcript | ENST00000371628.8 | protein_coding | 5/10 | chrX | 118993129 | ||||||
| chrX:118993129
|
C | CCA | 1 | a0001c0002t0001g0042 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.1415+2569_1415+257 others(6): Show |
LONRF3 | ENSG00000175556.17 | transcript | ENST00000371628.8 | protein_coding | 5/10 | chrX | 118993129 | ||||||
| chrX:118993193
|
T | A | 116 | a0001c0001t0001g0152a0001c0002t0001g0003a0001c0002t0001g0004others(113): Show | 127 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(124): Show |
intron_variant | MODIFIER | c.1415+2633T>A | LONRF3 | ENSG00000175556.17 | transcript | ENST00000371628.8 | protein_coding | 5/10 | chrX | 118993193 | ||||||
| chrX:118993435
|
T | G | 10 | a0001c0002t0001g0017a0001c0002t0001g0122a0001c0002t0001g0123others(7): Show | 11 | HG02055.hp1 HG02257.hp1 HG02895.hp1 others(8): Show |
intron_variant | MODIFIER | c.1415+2875T>G | LONRF3 | ENSG00000175556.17 | transcript | ENST00000371628.8 | protein_coding | 5/10 | chrX | 118993435 | ||||||
| chrX:118993562
|
A | G | 3 | a0001c0002t0001g0116a0001c0002t0001g0117a0001c0002t0005g0028 | 3 | HG02145.hp1 HG02809.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.1415+3002A>G | LONRF3 | ENSG00000175556.17 | transcript | ENST00000371628.8 | protein_coding | 5/10 | chrX | 118993562 | ||||||
| chrX:118993604
|
TG | T | 1 | a0001c0003t0002g0066 | 1 | NA18997.hp1 | intron_variant | MODIFIER | c.1415+3049delG | LONRF3 | ENSG00000175556.17 | transcript | ENST00000371628.8 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chrX | 118993604 | |||||
| chrX:118994056
|
A | T | 119 | a0001c0001t0001g0152a0001c0002t0001g0003a0001c0002t0001g0004others(116): Show | 130 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(127): Show |
intron_variant | MODIFIER | c.1415+3496A>T | LONRF3 | ENSG00000175556.17 | transcript | ENST00000371628.8 | protein_coding | 5/10 | chrX | 118994056 | ||||||
| chrX:118994173
|
C | T | 1 | a0001c0003t0001g0266 | 1 | HG01517.hp1 | intron_variant | MODIFIER | c.1415+3613C>T | LONRF3 | ENSG00000175556.17 | transcript | ENST00000371628.8 | protein_coding | 5/10 | chrX | 118994173 | ||||||
| chrX:118994177
|
A | G | 3 | a0001c0001t0002g0078a0001c0001t0002g0079a0001c0001t0002g0092 | 3 | NA18972.hp1 NA19002.hp2 NA19080.hp2 |
intron_variant | MODIFIER | c.1415+3617A>G | LONRF3 | ENSG00000175556.17 | transcript | ENST00000371628.8 | protein_coding | 5/10 | chrX | 118994177 | ||||||
| chrX:118994228
|
T | G | 10 | a0001c0002t0001g0005a0001c0002t0001g0022a0001c0002t0001g0161others(7): Show | 12 | HG01109.hp1 HG01243.hp1 HG02109.hp1 others(9): Show |
intron_variant | MODIFIER | c.1415+3668T>G | LONRF3 | ENSG00000175556.17 | transcript | ENST00000371628.8 | protein_coding | 5/10 | chrX | 118994228 | ||||||
| chrX:118994326
|
T | TA | 1 | a0001c0003t0002g0066 | 1 | NA18997.hp1 | intron_variant | MODIFIER | c.1415+3769dupA | LONRF3 | ENSG00000175556.17 | transcript | ENST00000371628.8 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chrX | 118994326 | |||||
| chrX:118994366
|
C | CA | 1 | a0001c0003t0002g0066 | 1 | NA18997.hp1 | intron_variant | MODIFIER | c.1415+3810dupA | LONRF3 | ENSG00000175556.17 | transcript | ENST00000371628.8 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chrX | 118994366 | |||||
| chrX:118994376
|
A | AG | 1 | a0001c0003t0002g0066 | 1 | NA18997.hp1 | intron_variant | MODIFIER | c.1415+3820dupG | LONRF3 | ENSG00000175556.17 | transcript | ENST00000371628.8 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chrX | 118994376 | |||||
| chrX:118994408
|
A | AT | 116 | a0001c0001t0001g0152a0001c0002t0001g0003a0001c0002t0001g0004others(113): Show | 127 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(124): Show |
intron_variant | MODIFIER | c.1415+3861dupT | LONRF3 | ENSG00000175556.17 | transcript | ENST00000371628.8 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chrX | 118994408 | |||||
| chrX:118994456
|
C | T | 1 | a0001c0003t0001g0183 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.1415+3896C>T | LONRF3 | ENSG00000175556.17 | transcript | ENST00000371628.8 | protein_coding | 5/10 | chrX | 118994456 | ||||||
| chrX:118994468
|
A | G | 2 | a0001c0002t0001g0023a0001c0002t0001g0049 | 2 | HG01106.hp1 HG02717.hp1 |
intron_variant | MODIFIER | c.1415+3908A>G | LONRF3 | ENSG00000175556.17 | transcript | ENST00000371628.8 | protein_coding | 5/10 | chrX | 118994468 | ||||||
| chrX:118994506
|
G | A | 1 | a0001c0002t0005g0028 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.1415+3946G>A | LONRF3 | ENSG00000175556.17 | transcript | ENST00000371628.8 | protein_coding | 5/10 | chrX | 118994506 | ||||||
| chrX:118994526
|
C | T | 1 | a0001c0002t0001g0147 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.1415+3966C>T | LONRF3 | ENSG00000175556.17 | transcript | ENST00000371628.8 | protein_coding | 5/10 | chrX | 118994526 | ||||||
| chrX:118994569
|
AT | A | 1 | a0001c0003t0002g0066 | 1 | NA18997.hp1 | intron_variant | MODIFIER | c.1415+4014delT | LONRF3 | ENSG00000175556.17 | transcript | ENST00000371628.8 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chrX | 118994569 | |||||
| chrX:118994601
|
C | T | 3 | a0001c0002t0001g0116a0001c0002t0001g0117a0001c0002t0005g0028 | 3 | HG02145.hp1 HG02809.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.1415+4041C>T | LONRF3 | ENSG00000175556.17 | transcript | ENST00000371628.8 | protein_coding | 5/10 | chrX | 118994601 | ||||||
| chrX:118994901
|
G | A | 1 | a0001c0003t0002g0271 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.1415+4341G>A | LONRF3 | ENSG00000175556.17 | transcript | ENST00000371628.8 | protein_coding | 5/10 | chrX | 118994901 | ||||||
| chrX:118995051
|
T | G | 13 | a0001c0002t0001g0017a0001c0002t0001g0116a0001c0002t0001g0117others(10): Show | 14 | HG02055.hp1 HG02145.hp1 HG02257.hp1 others(11): Show |
intron_variant | MODIFIER | c.1415+4491T>G | LONRF3 | ENSG00000175556.17 | transcript | ENST00000371628.8 | protein_coding | 5/10 | chrX | 118995051 | ||||||
| chrX:118995316
|
A | G | 1 | a0001c0001t0002g0114 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.1415+4756A>G | LONRF3 | ENSG00000175556.17 | transcript | ENST00000371628.8 | protein_coding | 5/10 | chrX | 118995316 | ||||||
| chrX:118995397
|
T | C | 1 | a0001c0002t0001g0123 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.1415+4837T>C | LONRF3 | ENSG00000175556.17 | transcript | ENST00000371628.8 | protein_coding | 5/10 | chrX | 118995397 | ||||||
| chrX:118995462
|
C | T | 5 | a0001c0001t0001g0204a0001c0001t0001g0205a0001c0001t0001g0221others(2): Show | 5 | HG00280.hp1 HG00733.hp1 HG01123.hp1 others(2): Show |
intron_variant | MODIFIER | c.1415+4902C>T | LONRF3 | ENSG00000175556.17 | transcript | ENST00000371628.8 | protein_coding | 5/10 | chrX | 118995462 | ||||||
| chrX:118995611
|
G | A | 1 | a0001c0001t0001g0221 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.1415+5051G>A | LONRF3 | ENSG00000175556.17 | transcript | ENST00000371628.8 | protein_coding | 5/10 | chrX | 118995611 | ||||||
| chrX:118995805
|
A | C | 6 | a0001c0002t0001g0023a0001c0002t0001g0024a0001c0002t0001g0043others(3): Show | 7 | HG01106.hp1 HG01891.hp1 HG02717.hp1 others(4): Show |
intron_variant | MODIFIER | c.1415+5245A>C | LONRF3 | ENSG00000175556.17 | transcript | ENST00000371628.8 | protein_coding | 5/10 | chrX | 118995805 | ||||||
| chrX:118996029
|
G | T | 1 | a0001c0002t0001g0135 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.1415+5469G>T | LONRF3 | ENSG00000175556.17 | transcript | ENST00000371628.8 | protein_coding | 5/10 | chrX | 118996029 | ||||||
| chrX:118996100
|
A | G | 3 | a0001c0002t0001g0116a0001c0002t0001g0117a0001c0002t0005g0028 | 3 | HG02145.hp1 HG02809.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.1415+5540A>G | LONRF3 | ENSG00000175556.17 | transcript | ENST00000371628.8 | protein_coding | 5/10 | chrX | 118996100 | ||||||
| chrX:118996105
|
G | A | 10 | a0001c0002t0001g0185a0001c0002t0003g0187a0001c0002t0003g0188others(7): Show | 10 | HG01884.hp1 HG02622.hp1 HG02622.hp2 others(7): Show |
intron_variant | MODIFIER | c.1415+5545G>A | LONRF3 | ENSG00000175556.17 | transcript | ENST00000371628.8 | protein_coding | 5/10 | chrX | 118996105 | ||||||
| chrX:118996166
|
T | C | 1 | a0001c0002t0001g0125 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.1415+5606T>C | LONRF3 | ENSG00000175556.17 | transcript | ENST00000371628.8 | protein_coding | 5/10 | chrX | 118996166 | ||||||
| chrX:118996217
|
G | A | 100 | a0001c0001t0001g0152a0001c0002t0001g0003a0001c0002t0001g0004others(97): Show | 109 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(106): Show |
intron_variant | MODIFIER | c.1415+5657G>A | LONRF3 | ENSG00000175556.17 | transcript | ENST00000371628.8 | protein_coding | 5/10 | chrX | 118996217 | ||||||
| chrX:118996478
|
A | G | 3 | a0001c0002t0001g0154a0001c0002t0001g0156a0001c0002t0001g0160 | 3 | HG03017.hp1 HG03654.hp1 HG03710.hp1 |
intron_variant | MODIFIER | c.1415+5918A>G | LONRF3 | ENSG00000175556.17 | transcript | ENST00000371628.8 | protein_coding | 5/10 | chrX | 118996478 | ||||||
| chrX:118996660
|
T | C | 275 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0006others(272): Show | 301 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(298): Show |
intron_variant | MODIFIER | c.1415+6100T>C | LONRF3 | ENSG00000175556.17 | transcript | ENST00000371628.8 | protein_coding | 5/10 | chrX | 118996660 | ||||||
| chrX:118996704
|
C | T | 1 | a0001c0001t0001g0242 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.1415+6144C>T | LONRF3 | ENSG00000175556.17 | transcript | ENST00000371628.8 | protein_coding | 5/10 | chrX | 118996704 | ||||||
| chrX:118996767
|
A | G | 6 | a0001c0002t0001g0144a0001c0002t0001g0145a0001c0002t0001g0146others(3): Show | 6 | HG02083.hp1 NA18941.hp2 NA18948.hp1 others(3): Show |
intron_variant | MODIFIER | c.1415+6207A>G | LONRF3 | ENSG00000175556.17 | transcript | ENST00000371628.8 | protein_coding | 5/10 | chrX | 118996767 | ||||||
| chrX:118996921
|
C | CA | 6 | a0001c0001t0001g0027a0001c0001t0001g0111a0001c0001t0001g0240others(3): Show | 6 | HG00597.hp1 HG01256.hp1 HG01891.hp2 others(3): Show |
intron_variant | MODIFIER | c.1415+6378dupA | LONRF3 | ENSG00000175556.17 | transcript | ENST00000371628.8 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chrX | 118996921 | |||||
| chrX:118996921
|
C | CAA | 1 | a0001c0002t0001g0185 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.1415+6377_1415+637 others(6): Show |
LONRF3 | ENSG00000175556.17 | transcript | ENST00000371628.8 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chrX | 118996921 | |||||
| chrX:118996921
|
CA | C | 78 | a0001c0001t0001g0152a0001c0001t0001g0254a0001c0001t0002g0077others(75): Show | 85 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(82): Show |
intron_variant | MODIFIER | c.1415+6378delA | LONRF3 | ENSG00000175556.17 | transcript | ENST00000371628.8 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chrX | 118996921 | |||||
| chrX:118996921
|
CAA | C | 1 | a0001c0002t0004g0021 | 2 | HG01891.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.1415+6377_1415+637 others(6): Show |
LONRF3 | ENSG00000175556.17 | transcript | ENST00000371628.8 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chrX | 118996921 | |||||
| chrX:118997048
|
A | G | 22 | a0001c0002t0001g0008a0001c0002t0001g0009a0001c0002t0001g0029others(19): Show | 24 | HG00408.hp1 HG00423.hp1 HG00544.hp2 others(21): Show |
intron_variant | MODIFIER | c.1415+6488A>G | LONRF3 | ENSG00000175556.17 | transcript | ENST00000371628.8 | protein_coding | 5/10 | chrX | 118997048 | ||||||
| chrX:118997109
|
G | GA | 1 | a0001c0001t0002g0198 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.1415+6557dupA | LONRF3 | ENSG00000175556.17 | transcript | ENST00000371628.8 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chrX | 118997109 | |||||
| chrX:118997117
|
AC | A | 1 | a0001c0009t0002g0093 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.1415+6558delC | LONRF3 | ENSG00000175556.17 | transcript | ENST00000371628.8 | protein_coding | 5/10 | chrX | 118997117 | ||||||
| chrX:118997468
|
C | A | 1 | a0001c0001t0009g0208 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.1415+6908C>A | LONRF3 | ENSG00000175556.17 | transcript | ENST00000371628.8 | protein_coding | 5/10 | chrX | 118997468 | ||||||
| chrX:118997722
|
T | G | 1 | a0001c0004t0001g0277 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.1415+7162T>G | LONRF3 | ENSG00000175556.17 | transcript | ENST00000371628.8 | protein_coding | 5/10 | chrX | 118997722 | ||||||
| chrX:118997785
|
A | T | 3 | a0001c0001t0001g0268a0001c0001t0001g0269a0001c0001t0001g0270 | 3 | HG01934.hp1 HG02132.hp1 NA19057.hp2 |
intron_variant | MODIFIER | c.1415+7225A>T | LONRF3 | ENSG00000175556.17 | transcript | ENST00000371628.8 | protein_coding | 5/10 | chrX | 118997785 | ||||||
| chrX:118997865
|
A | G | 102 | a0001c0001t0001g0152a0001c0002t0001g0003a0001c0002t0001g0004others(99): Show | 111 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(108): Show |
intron_variant | MODIFIER | c.1415+7305A>G | LONRF3 | ENSG00000175556.17 | transcript | ENST00000371628.8 | protein_coding | 5/10 | chrX | 118997865 | ||||||
| chrX:118997963
|
C | CA | 1 | a0001c0002t0004g0021 | 2 | HG01891.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.1415+7409dupA | LONRF3 | ENSG00000175556.17 | transcript | ENST00000371628.8 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chrX | 118997963 | |||||
| chrX:118998097
|
T | C | 3 | a0001c0003t0001g0094a0001c0003t0001g0097a0001c0003t0001g0098 | 3 | HG01099.hp1 HG01167.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.1415+7537T>C | LONRF3 | ENSG00000175556.17 | transcript | ENST00000371628.8 | protein_coding | 5/10 | chrX | 118998097 | ||||||
| chrX:118998185
|
C | CA | 122 | a0001c0001t0001g0152a0001c0002t0001g0003a0001c0002t0001g0004others(119): Show | 133 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(130): Show |
intron_variant | MODIFIER | c.1415+7626dupA | LONRF3 | ENSG00000175556.17 | transcript | ENST00000371628.8 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chrX | 118998185 | |||||
| chrX:118998259
|
A | G | 1 | a0001c0001t0002g0077 | 1 | NA19074.hp1 | intron_variant | MODIFIER | c.1415+7699A>G | LONRF3 | ENSG00000175556.17 | transcript | ENST00000371628.8 | protein_coding | 5/10 | chrX | 118998259 | ||||||
| chrX:118998320
|
G | C | 3 | a0001c0003t0002g0031a0001c0003t0002g0035a0001c0003t0002g0036 | 3 | HG02027.hp1 NA18941.hp1 NA18943.hp1 |
intron_variant | MODIFIER | c.1415+7760G>C | LONRF3 | ENSG00000175556.17 | transcript | ENST00000371628.8 | protein_coding | 5/10 | chrX | 118998320 | ||||||
| chrX:118998453
|
TG | T | 1 | a0001c0002t0001g0038 | 1 | NA18991.hp2 | intron_variant | MODIFIER | c.1416-7662delG | LONRF3 | ENSG00000175556.17 | transcript | ENST00000371628.8 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chrX | 118998453 | |||||
| chrX:118998470
|
A | AG | 1 | a0001c0001t0002g0067 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.1416-7646dupG | LONRF3 | ENSG00000175556.17 | transcript | ENST00000371628.8 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chrX | 118998470 | |||||
| chrX:118998500
|
G | A | 2 | a0001c0004t0001g0101a0001c0004t0001g0102 | 2 | HG02976.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.1416-7621G>A | LONRF3 | ENSG00000175556.17 | transcript | ENST00000371628.8 | protein_coding | 5/10 | chrX | 118998500 | ||||||
| chrX:118998515
|
G | A | 2 | a0001c0002t0001g0185a0001c0002t0003g0188 | 2 | HG02622.hp1 HG02818.hp2 |
intron_variant | MODIFIER | c.1416-7606G>A | LONRF3 | ENSG00000175556.17 | transcript | ENST00000371628.8 | protein_coding | 5/10 | chrX | 118998515 | ||||||
| chrX:118998724
|
C | A | 1 | a0001c0004t0001g0279 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1416-7397C>A | LONRF3 | ENSG00000175556.17 | transcript | ENST00000371628.8 | protein_coding | 5/10 | chrX | 118998724 | ||||||
| chrX:118998742
|
C | T | 1 | a0001c0001t0002g0076 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.1416-7379C>T | LONRF3 | ENSG00000175556.17 | transcript | ENST00000371628.8 | protein_coding | 5/10 | chrX | 118998742 | ||||||
| chrX:118998744
|
C | T | 1 | a0001c0002t0001g0135 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.1416-7377C>T | LONRF3 | ENSG00000175556.17 | transcript | ENST00000371628.8 | protein_coding | 5/10 | chrX | 118998744 | ||||||
| chrX:118998823
|
C | A | 1 | a0001c0002t0005g0028 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.1416-7298C>A | LONRF3 | ENSG00000175556.17 | transcript | ENST00000371628.8 | protein_coding | 5/10 | chrX | 118998823 | ||||||
| chrX:118998940
|
G | A | 10 | a0001c0002t0001g0017a0001c0002t0001g0122a0001c0002t0001g0123others(7): Show | 11 | HG02055.hp1 HG02257.hp1 HG02895.hp1 others(8): Show |
intron_variant | MODIFIER | c.1416-7181G>A | LONRF3 | ENSG00000175556.17 | transcript | ENST00000371628.8 | protein_coding | 5/10 | chrX | 118998940 | ||||||
| chrX:118999058
|
G | A | 1 | a0001c0002t0003g0025 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.1416-7063G>A | LONRF3 | ENSG00000175556.17 | transcript | ENST00000371628.8 | protein_coding | 5/10 | chrX | 118999058 | ||||||
| chrX:118999113
|
C | T | 1 | a0001c0002t0006g0184 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.1416-7008C>T | LONRF3 | ENSG00000175556.17 | transcript | ENST00000371628.8 | protein_coding | 5/10 | chrX | 118999113 | ||||||
| chrX:118999145
|
C | T | 1 | a0001c0001t0009g0208 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.1416-6976C>T | LONRF3 | ENSG00000175556.17 | transcript | ENST00000371628.8 | protein_coding | 5/10 | chrX | 118999145 | ||||||
| chrX:118999148
|
T | A | 1 | a0001c0001t0001g0064 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.1416-6973T>A | LONRF3 | ENSG00000175556.17 | transcript | ENST00000371628.8 | protein_coding | 5/10 | chrX | 118999148 | ||||||
| chrX:118999228
|
A | G | 10 | a0001c0002t0001g0005a0001c0002t0001g0022a0001c0002t0001g0161others(7): Show | 12 | HG01109.hp1 HG01243.hp1 HG02109.hp1 others(9): Show |
intron_variant | MODIFIER | c.1416-6893A>G | LONRF3 | ENSG00000175556.17 | transcript | ENST00000371628.8 | protein_coding | 5/10 | chrX | 118999228 | ||||||
| chrX:118999334
|
C | G | 2 | a0001c0001t0002g0057a0001c0001t0002g0104 | 2 | HG01928.hp1 HG01978.hp1 |
intron_variant | MODIFIER | c.1416-6787C>G | LONRF3 | ENSG00000175556.17 | transcript | ENST00000371628.8 | protein_coding | 5/10 | chrX | 118999334 | ||||||
| chrX:118999466
|
GTAGACT | G | 10 | a0001c0002t0001g0017a0001c0002t0001g0122a0001c0002t0001g0123others(7): Show | 11 | HG02055.hp1 HG02257.hp1 HG02895.hp1 others(8): Show |
intron_variant | MODIFIER | c.1416-6653_1416-664 others(10): Show |
LONRF3 | ENSG00000175556.17 | transcript | ENST00000371628.8 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chrX | 118999466 | |||||
| chrX:118999661
|
A | C | 1 | a0001c0009t0002g0093 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.1416-6460A>C | LONRF3 | ENSG00000175556.17 | transcript | ENST00000371628.8 | protein_coding | 5/10 | chrX | 118999661 | ||||||
| chrX:118999727
|
AC | A | 1 | a0001c0003t0002g0066 | 1 | NA18997.hp1 | intron_variant | MODIFIER | c.1416-6389delC | LONRF3 | ENSG00000175556.17 | transcript | ENST00000371628.8 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chrX | 118999727 | |||||
| chrX:118999761
|
G | T | 1 | a0001c0001t0001g0264 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.1416-6360G>T | LONRF3 | ENSG00000175556.17 | transcript | ENST00000371628.8 | protein_coding | 5/10 | chrX | 118999761 | ||||||
| chrX:118999825
|
C | T | 1 | a0001c0009t0002g0093 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.1416-6296C>T | LONRF3 | ENSG00000175556.17 | transcript | ENST00000371628.8 | protein_coding | 5/10 | chrX | 118999825 | ||||||
| chrX:119000169
|
T | A | 1 | a0001c0001t0001g0020 | 2 | HG03491.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.1416-5952T>A | LONRF3 | ENSG00000175556.17 | transcript | ENST00000371628.8 | protein_coding | 5/10 | chrX | 119000169 | ||||||
| chrX:119000300
|
T | A | 1 | a0001c0001t0001g0234 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.1416-5821T>A | LONRF3 | ENSG00000175556.17 | transcript | ENST00000371628.8 | protein_coding | 5/10 | chrX | 119000300 | ||||||
| chrX:119000324
|
A | G | 2 | a0001c0002t0001g0154a0001c0002t0001g0160 | 2 | HG03017.hp1 HG03710.hp1 |
intron_variant | MODIFIER | c.1416-5797A>G | LONRF3 | ENSG00000175556.17 | transcript | ENST00000371628.8 | protein_coding | 5/10 | chrX | 119000324 | ||||||
| chrX:119000478
|
C | G | 10 | a0001c0002t0001g0185a0001c0002t0003g0187a0001c0002t0003g0188others(7): Show | 10 | HG01884.hp1 HG02622.hp1 HG02622.hp2 others(7): Show |
intron_variant | MODIFIER | c.1416-5643C>G | LONRF3 | ENSG00000175556.17 | transcript | ENST00000371628.8 | protein_coding | 5/10 | chrX | 119000478 | ||||||
| chrX:119000566
|
C | T | 1 | a0001c0001t0001g0152 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.1416-5555C>T | LONRF3 | ENSG00000175556.17 | transcript | ENST00000371628.8 | protein_coding | 5/10 | chrX | 119000566 | ||||||
| chrX:119000774
|
ATTCTCTC | A | 1 | a0001c0001t0002g0103 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.1416-5345_1416-533 others(11): Show |
LONRF3 | ENSG00000175556.17 | transcript | ENST00000371628.8 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chrX | 119000774 | |||||
| chrX:119000775
|
T | TTCTC | 1 | a0001c0003t0001g0171 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.1416-5285_1416-528 others(8): Show |
LONRF3 | ENSG00000175556.17 | transcript | ENST00000371628.8 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chrX | 119000775 | |||||
| chrX:119000775
|
TTC | T | 1 | a0001c0001t0002g0089 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.1416-5283_1416-528 others(6): Show |
LONRF3 | ENSG00000175556.17 | transcript | ENST00000371628.8 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chrX | 119000775 | |||||
| chrX:119000775
|
TTCTC | T | 3 | a0001c0003t0001g0181a0001c0003t0001g0183a0001c0003t0002g0271 | 3 | HG00741.hp1 HG01168.hp1 HG03688.hp1 |
intron_variant | MODIFIER | c.1416-5285_1416-528 others(8): Show |
LONRF3 | ENSG00000175556.17 | transcript | ENST00000371628.8 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chrX | 119000775 | |||||
| chrX:119000775
|
TTCTCTC | T | 8 | a0001c0001t0002g0055a0001c0001t0002g0061a0001c0001t0002g0075others(5): Show | 8 | HG01074.hp1 HG01169.hp1 HG02258.hp1 others(5): Show |
intron_variant | MODIFIER | c.1416-5287_1416-528 others(10): Show |
LONRF3 | ENSG00000175556.17 | transcript | ENST00000371628.8 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chrX | 119000775 | |||||
| chrX:119000775
|
TTCTCTCT others(1): Show |
T | 14 | a0001c0001t0001g0013a0001c0001t0001g0064a0001c0001t0001g0096others(11): Show | 14 | HG00408.hp2 HG00423.hp2 HG00597.hp2 others(11): Show |
intron_variant | MODIFIER | c.1416-5289_1416-528 others(12): Show |
LONRF3 | ENSG00000175556.17 | transcript | ENST00000371628.8 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chrX | 119000775 | |||||
| chrX:119000775
|
TTCTCTCT others(3): Show |
T | 18 | a0001c0001t0001g0001a0001c0001t0001g0109a0001c0001t0002g0001others(15): Show | 20 | HG00099.hp2 HG00621.hp1 HG01993.hp2 others(17): Show |
intron_variant | MODIFIER | c.1416-5291_1416-528 others(14): Show |
LONRF3 | ENSG00000175556.17 | transcript | ENST00000371628.8 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chrX | 119000775 | |||||
| chrX:119000775
|
TTCTCTCT others(5): Show |
T | 8 | a0001c0001t0002g0057a0001c0001t0002g0069a0001c0001t0002g0091others(5): Show | 8 | HG00673.hp1 HG01928.hp1 HG02109.hp2 others(5): Show |
intron_variant | MODIFIER | c.1416-5293_1416-528 others(16): Show |
LONRF3 | ENSG00000175556.17 | transcript | ENST00000371628.8 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chrX | 119000775 | |||||
| chrX:119000775
|
TTCTCTCT others(7): Show |
T | 14 | a0001c0001t0001g0107a0001c0001t0002g0010a0001c0001t0002g0012others(11): Show | 18 | HG01261.hp1 HG01978.hp1 HG01981.hp2 others(15): Show |
intron_variant | MODIFIER | c.1416-5295_1416-528 others(18): Show |
LONRF3 | ENSG00000175556.17 | transcript | ENST00000371628.8 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chrX | 119000775 | |||||
| chrX:119000775
|
TTCTCTCT others(9): Show |
T | 20 | a0001c0001t0001g0245a0001c0001t0001g0262a0001c0001t0002g0068others(17): Show | 23 | HG00438.hp2 HG00639.hp1 HG01081.hp2 others(20): Show |
intron_variant | MODIFIER | c.1416-5297_1416-528 others(20): Show |
LONRF3 | ENSG00000175556.17 | transcript | ENST00000371628.8 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chrX | 119000775 | |||||
| chrX:119000775
|
TTCTCTCT others(11): Show |
T | 23 | a0001c0001t0002g0082a0001c0002t0001g0003a0001c0002t0001g0009others(20): Show | 26 | HG00140.hp1 HG01192.hp1 HG02451.hp1 others(23): Show |
intron_variant | MODIFIER | c.1416-5299_1416-528 others(22): Show |
LONRF3 | ENSG00000175556.17 | transcript | ENST00000371628.8 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chrX | 119000775 | |||||
| chrX:119000775
|
TTCTCTCT others(13): Show |
T | 35 | a0001c0001t0001g0112a0001c0002t0001g0018a0001c0002t0001g0019others(32): Show | 36 | HG00099.hp1 HG00323.hp1 HG00642.hp1 others(33): Show |
intron_variant | MODIFIER | c.1416-5301_1416-528 others(24): Show |
LONRF3 | ENSG00000175556.17 | transcript | ENST00000371628.8 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chrX | 119000775 | |||||
| chrX:119000775
|
TTCTCTCT others(15): Show |
T | 21 | a0001c0001t0001g0026a0001c0001t0001g0047a0001c0001t0001g0215others(18): Show | 24 | HG00408.hp1 HG00423.hp1 HG00544.hp2 others(21): Show |
intron_variant | MODIFIER | c.1416-5303_1416-528 others(26): Show |
LONRF3 | ENSG00000175556.17 | transcript | ENST00000371628.8 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chrX | 119000775 | |||||
| chrX:119000775
|
TTCTCTCT others(17): Show |
T | 16 | a0001c0001t0001g0002a0001c0001t0001g0030a0001c0001t0001g0152others(13): Show | 19 | HG02083.hp1 HG02280.hp1 HG02738.hp1 others(16): Show |
intron_variant | MODIFIER | c.1416-5305_1416-528 others(28): Show |
LONRF3 | ENSG00000175556.17 | transcript | ENST00000371628.8 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chrX | 119000775 | |||||
| chrX:119000775
|
TTCTCTCT others(19): Show |
T | 56 | a0001c0001t0001g0006a0001c0001t0001g0020a0001c0001t0001g0027others(53): Show | 60 | HG00544.hp1 HG00597.hp1 HG00609.hp1 others(57): Show |
intron_variant | MODIFIER | c.1416-5307_1416-528 others(30): Show |
LONRF3 | ENSG00000175556.17 | transcript | ENST00000371628.8 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chrX | 119000775 | |||||
| chrX:119000775
|
TTCTCTCT others(21): Show |
T | 18 | a0001c0001t0001g0007a0001c0001t0001g0209a0001c0001t0001g0210others(15): Show | 20 | HG00323.hp2 HG00438.hp1 HG01358.hp1 others(17): Show |
intron_variant | MODIFIER | c.1416-5309_1416-528 others(32): Show |
LONRF3 | ENSG00000175556.17 | transcript | ENST00000371628.8 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chrX | 119000775 | |||||
| chrX:119000775
|
TTCTCTCT others(23): Show |
T | 9 | a0001c0001t0001g0204a0001c0001t0001g0205a0001c0001t0001g0216others(6): Show | 9 | HG00280.hp1 HG00733.hp1 HG01123.hp1 others(6): Show |
intron_variant | MODIFIER | c.1416-5311_1416-528 others(34): Show |
LONRF3 | ENSG00000175556.17 | transcript | ENST00000371628.8 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chrX | 119000775 | |||||
| chrX:119000775
|
TTCTCTCT others(25): Show |
T | 14 | a0001c0002t0001g0017a0001c0002t0001g0116a0001c0002t0001g0117others(11): Show | 15 | HG02055.hp1 HG02145.hp1 HG02257.hp1 others(12): Show |
intron_variant | MODIFIER | c.1416-5313_1416-528 others(36): Show |
LONRF3 | ENSG00000175556.17 | transcript | ENST00000371628.8 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chrX | 119000775 | |||||
| chrX:119000775
|
TTCTCTCT others(29): Show |
T | 1 | a0001c0001t0001g0263 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.1416-5317_1416-528 others(40): Show |
LONRF3 | ENSG00000175556.17 | transcript | ENST00000371628.8 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chrX | 119000775 | |||||
| chrX:119000799
|
CTCT | C | 1 | a0001c0001t0002g0067 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.1416-5321_1416-531 others(7): Show |
LONRF3 | ENSG00000175556.17 | transcript | ENST00000371628.8 | protein_coding | 5/10 | chrX | 119000799 | ||||||
| chrX:119000849
|
C | T | 3 | a0001c0002t0001g0116a0001c0002t0001g0117a0001c0002t0005g0028 | 3 | HG02145.hp1 HG02809.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.1416-5272C>T | LONRF3 | ENSG00000175556.17 | transcript | ENST00000371628.8 | protein_coding | 5/10 | chrX | 119000849 | ||||||
| chrX:119000971
|
G | T | 22 | a0001c0002t0001g0008a0001c0002t0001g0009a0001c0002t0001g0029others(19): Show | 24 | HG00408.hp1 HG00423.hp1 HG00544.hp2 others(21): Show |
intron_variant | MODIFIER | c.1416-5150G>T | LONRF3 | ENSG00000175556.17 | transcript | ENST00000371628.8 | protein_coding | 5/10 | chrX | 119000971 | ||||||
| chrX:119001189
|
C | G | 27 | a0001c0001t0001g0020a0001c0001t0001g0111a0001c0001t0001g0234others(24): Show | 28 | HG00323.hp2 HG00609.hp1 HG00738.hp1 others(25): Show |
intron_variant | MODIFIER | c.1416-4932C>G | LONRF3 | ENSG00000175556.17 | transcript | ENST00000371628.8 | protein_coding | 5/10 | chrX | 119001189 | ||||||
| chrX:119001227
|
A | AG | 1 | a0001c0001t0002g0067 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.1416-4891dupG | LONRF3 | ENSG00000175556.17 | transcript | ENST00000371628.8 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chrX | 119001227 | |||||
| chrX:119001746
|
G | A | 1 | a0001c0003t0001g0266 | 1 | HG01517.hp1 | intron_variant | MODIFIER | c.1416-4375G>A | LONRF3 | ENSG00000175556.17 | transcript | ENST00000371628.8 | protein_coding | 5/10 | chrX | 119001746 | ||||||
| chrX:119001788
|
T | A | 2 | a0001c0002t0001g0024a0001c0002t0003g0025 | 2 | HG02886.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.1416-4333T>A | LONRF3 | ENSG00000175556.17 | transcript | ENST00000371628.8 | protein_coding | 5/10 | chrX | 119001788 | ||||||
| chrX:119001828
|
CT | C | 1 | a0001c0001t0002g0067 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.1416-4290delT | LONRF3 | ENSG00000175556.17 | transcript | ENST00000371628.8 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chrX | 119001828 | |||||
| chrX:119001960
|
T | C | 70 | a0001c0001t0001g0152a0001c0002t0001g0003a0001c0002t0001g0004others(67): Show | 77 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(74): Show |
intron_variant | MODIFIER | c.1416-4161T>C | LONRF3 | ENSG00000175556.17 | transcript | ENST00000371628.8 | protein_coding | 5/10 | chrX | 119001960 | ||||||
| chrX:119002005
|
C | T | 1 | a0001c0002t0001g0267 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.1416-4116C>T | LONRF3 | ENSG00000175556.17 | transcript | ENST00000371628.8 | protein_coding | 5/10 | chrX | 119002005 | ||||||
| chrX:119002262
|
C | T | 1 | a0001c0001t0002g0054 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.1416-3859C>T | LONRF3 | ENSG00000175556.17 | transcript | ENST00000371628.8 | protein_coding | 5/10 | chrX | 119002262 | ||||||
| chrX:119002285
|
C | G | 10 | a0001c0002t0001g0017a0001c0002t0001g0122a0001c0002t0001g0123others(7): Show | 11 | HG02055.hp1 HG02257.hp1 HG02895.hp1 others(8): Show |
intron_variant | MODIFIER | c.1416-3836C>G | LONRF3 | ENSG00000175556.17 | transcript | ENST00000371628.8 | protein_coding | 5/10 | chrX | 119002285 | ||||||
| chrX:119002311
|
C | T | 5 | a0001c0001t0001g0096a0001c0001t0001g0112a0001c0003t0001g0094others(2): Show | 5 | HG01099.hp1 HG01167.hp1 HG01169.hp2 others(2): Show |
intron_variant | MODIFIER | c.1416-3810C>T | LONRF3 | ENSG00000175556.17 | transcript | ENST00000371628.8 | protein_coding | 5/10 | chrX | 119002311 | ||||||
| chrX:119002451
|
A | G | 123 | a0001c0001t0001g0152a0001c0002t0001g0003a0001c0002t0001g0004others(120): Show | 134 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(131): Show |
intron_variant | MODIFIER | c.1416-3670A>G | LONRF3 | ENSG00000175556.17 | transcript | ENST00000371628.8 | protein_coding | 5/10 | chrX | 119002451 | ||||||
| chrX:119002734
|
G | A | 1 | a0001c0003t0002g0271 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.1416-3387G>A | LONRF3 | ENSG00000175556.17 | transcript | ENST00000371628.8 | protein_coding | 5/10 | chrX | 119002734 | ||||||
| chrX:119002806
|
T | A | 3 | a0001c0002t0001g0116a0001c0002t0001g0117a0001c0002t0005g0028 | 3 | HG02145.hp1 HG02809.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.1416-3315T>A | LONRF3 | ENSG00000175556.17 | transcript | ENST00000371628.8 | protein_coding | 5/10 | chrX | 119002806 | ||||||
| chrX:119003362
|
C | T | 6 | a0001c0001t0002g0011a0001c0001t0002g0062a0001c0001t0002g0065others(3): Show | 7 | HG00621.hp1 NA18952.hp1 NA18963.hp2 others(4): Show |
intron_variant | MODIFIER | c.1416-2759C>T | LONRF3 | ENSG00000175556.17 | transcript | ENST00000371628.8 | protein_coding | 5/10 | chrX | 119003362 | ||||||
| chrX:119003500
|
C | A | 80 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0007others(77): Show | 88 | HG00280.hp1 HG00323.hp2 HG00438.hp1 others(85): Show |
intron_variant | MODIFIER | c.1416-2621C>A | LONRF3 | ENSG00000175556.17 | transcript | ENST00000371628.8 | protein_coding | 5/10 | chrX | 119003500 | ||||||
| chrX:119003750
|
T | C | 1 | a0001c0001t0001g0209 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.1416-2371T>C | LONRF3 | ENSG00000175556.17 | transcript | ENST00000371628.8 | protein_coding | 5/10 | chrX | 119003750 | ||||||
| chrX:119003856
|
C | T | 70 | a0001c0001t0001g0152a0001c0002t0001g0003a0001c0002t0001g0004others(67): Show | 77 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(74): Show |
intron_variant | MODIFIER | c.1416-2265C>T | LONRF3 | ENSG00000175556.17 | transcript | ENST00000371628.8 | protein_coding | 5/10 | chrX | 119003856 | ||||||
| chrX:119003980
|
CGTGT | C | 10 | a0001c0002t0001g0017a0001c0002t0001g0122a0001c0002t0001g0123others(7): Show | 11 | HG02055.hp1 HG02257.hp1 HG02895.hp1 others(8): Show |
intron_variant | MODIFIER | c.1416-2134_1416-213 others(8): Show |
LONRF3 | ENSG00000175556.17 | transcript | ENST00000371628.8 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chrX | 119003980 | |||||
| chrX:119003985
|
G | C | 1 | a0001c0001t0002g0053 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.1416-2136G>C | LONRF3 | ENSG00000175556.17 | transcript | ENST00000371628.8 | protein_coding | 5/10 | chrX | 119003985 | ||||||
| chrX:119004100
|
GT | G | 10 | a0001c0002t0001g0017a0001c0002t0001g0122a0001c0002t0001g0123others(7): Show | 11 | HG02055.hp1 HG02257.hp1 HG02895.hp1 others(8): Show |
intron_variant | MODIFIER | c.1416-2014delT | LONRF3 | ENSG00000175556.17 | transcript | ENST00000371628.8 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chrX | 119004100 | |||||
| chrX:119004233
|
A | G | 2 | a0001c0004t0001g0192a0001c0004t0001g0197 | 2 | HG02622.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.1416-1888A>G | LONRF3 | ENSG00000175556.17 | transcript | ENST00000371628.8 | protein_coding | 5/10 | chrX | 119004233 | ||||||
| chrX:119004464
|
A | G | 2 | a0001c0002t0001g0023a0001c0002t0001g0049 | 2 | HG01106.hp1 HG02717.hp1 |
intron_variant | MODIFIER | c.1416-1657A>G | LONRF3 | ENSG00000175556.17 | transcript | ENST00000371628.8 | protein_coding | 5/10 | chrX | 119004464 | ||||||
| chrX:119004568
|
C | A | 1 | a0001c0001t0001g0100 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.1416-1553C>A | LONRF3 | ENSG00000175556.17 | transcript | ENST00000371628.8 | protein_coding | 5/10 | chrX | 119004568 | ||||||
| chrX:119004576
|
G | A | 1 | a0001c0009t0002g0093 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.1416-1545G>A | LONRF3 | ENSG00000175556.17 | transcript | ENST00000371628.8 | protein_coding | 5/10 | chrX | 119004576 | ||||||
| chrX:119004851
|
G | A | 4 | a0001c0002t0001g0128a0001c0002t0001g0138a0001c0002t0001g0139others(1): Show | 4 | HG02109.hp2 HG02896.hp2 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.1416-1270G>A | LONRF3 | ENSG00000175556.17 | transcript | ENST00000371628.8 | protein_coding | 5/10 | chrX | 119004851 | ||||||
| chrX:119005060
|
T | G | 12 | a0001c0002t0001g0185a0001c0002t0003g0187a0001c0002t0003g0188others(9): Show | 12 | HG01884.hp1 HG02559.hp1 HG02622.hp1 others(9): Show |
intron_variant | MODIFIER | c.1416-1061T>G | LONRF3 | ENSG00000175556.17 | transcript | ENST00000371628.8 | protein_coding | 5/10 | chrX | 119005060 | ||||||
| chrX:119005340
|
A | G | 1 | a0001c0002t0001g0023 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.1416-781A>G | LONRF3 | ENSG00000175556.17 | transcript | ENST00000371628.8 | protein_coding | 5/10 | chrX | 119005340 | ||||||
| chrX:119005428
|
A | ATG | 11 | a0001c0002t0001g0017a0001c0002t0001g0049a0001c0002t0001g0122others(8): Show | 12 | HG02055.hp1 HG02257.hp1 HG02451.hp1 others(9): Show |
intron_variant | MODIFIER | c.1416-691_1416-690d others(4): Show |
LONRF3 | ENSG00000175556.17 | transcript | ENST00000371628.8 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chrX | 119005428 | |||||
| chrX:119005430
|
G | GTA | 1 | a0001c0002t0001g0168 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1416-683_1416-682d others(4): Show |
LONRF3 | ENSG00000175556.17 | transcript | ENST00000371628.8 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chrX | 119005430 | |||||
| chrX:119005656
|
G | GT | 1 | a0001c0001t0002g0060 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.1416-458dupT | LONRF3 | ENSG00000175556.17 | transcript | ENST00000371628.8 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chrX | 119005656 | |||||
| chrX:119005778
|
G | A | 1 | a0001c0002t0005g0028 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.1416-343G>A | LONRF3 | ENSG00000175556.17 | transcript | ENST00000371628.8 | protein_coding | 5/10 | chrX | 119005778 | ||||||
| chrX:119005852
|
C | CA | 1 | a0001c0001t0002g0060 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.1416-263dupA | LONRF3 | ENSG00000175556.17 | transcript | ENST00000371628.8 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chrX | 119005852 | |||||
| chrX:119006017
|
C | T | 1 | a0001c0001t0002g0090 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.1416-104C>T | LONRF3 | ENSG00000175556.17 | transcript | ENST00000371628.8 | protein_coding | 5/10 | chrX | 119006017 | ||||||
| chrX:119006345
|
C | CGGCACT | 1 | a0001c0004t0001g0258 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.1530+112_1530+117d others(8): Show |
LONRF3 | ENSG00000175556.17 | transcript | ENST00000371628.8 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chrX | 119006345 | |||||
| chrX:119006398
|
C | CT | 29 | a0001c0001t0001g0109a0001c0001t0001g0207a0001c0001t0001g0230others(26): Show | 30 | HG00438.hp2 HG00597.hp2 HG00621.hp1 others(27): Show |
intron_variant | MODIFIER | c.1530+184dupT | LONRF3 | ENSG00000175556.17 | transcript | ENST00000371628.8 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chrX | 119006398 | |||||
| chrX:119006398
|
C | CTT | 11 | a0001c0002t0001g0017a0001c0002t0001g0049a0001c0002t0001g0122others(8): Show | 12 | HG00673.hp1 HG02055.hp1 HG02257.hp1 others(9): Show |
intron_variant | MODIFIER | c.1530+183_1530+184d others(4): Show |
LONRF3 | ENSG00000175556.17 | transcript | ENST00000371628.8 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chrX | 119006398 | |||||
| chrX:119006398
|
C | CTTT | 6 | a0001c0002t0001g0023a0001c0002t0001g0024a0001c0002t0001g0043others(3): Show | 7 | HG01106.hp1 HG01891.hp1 HG02809.hp1 others(4): Show |
intron_variant | MODIFIER | c.1530+182_1530+184d others(5): Show |
LONRF3 | ENSG00000175556.17 | transcript | ENST00000371628.8 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chrX | 119006398 | |||||
| chrX:119006398
|
C | T | 1 | a0001c0002t0001g0117 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1530+163C>T | LONRF3 | ENSG00000175556.17 | transcript | ENST00000371628.8 | protein_coding | 6/10 | chrX | 119006398 | ||||||
| chrX:119006398
|
CT | C | 16 | a0001c0001t0001g0152a0001c0001t0001g0217a0001c0001t0001g0227others(13): Show | 16 | HG01099.hp1 HG01167.hp1 HG01169.hp1 others(13): Show |
intron_variant | MODIFIER | c.1530+184delT | LONRF3 | ENSG00000175556.17 | transcript | ENST00000371628.8 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chrX | 119006398 | |||||
| chrX:119006562
|
G | A | 11 | a0001c0002t0001g0017a0001c0002t0001g0049a0001c0002t0001g0122others(8): Show | 12 | HG02055.hp1 HG02257.hp1 HG02451.hp1 others(9): Show |
intron_variant | MODIFIER | c.1530+327G>A | LONRF3 | ENSG00000175556.17 | transcript | ENST00000371628.8 | protein_coding | 6/10 | chrX | 119006562 | ||||||
| chrX:119006568
|
T | TTTTTG | 75 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0007others(72): Show | 83 | HG00280.hp1 HG00323.hp2 HG00438.hp1 others(80): Show |
intron_variant | MODIFIER | c.1530+366_1530+370d others(7): Show |
LONRF3 | ENSG00000175556.17 | transcript | ENST00000371628.8 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chrX | 119006568 | |||||
| chrX:119006568
|
T | TTTTTGTT others(3): Show |
8 | a0001c0001t0001g0047a0001c0001t0001g0096a0001c0001t0001g0243others(5): Show | 8 | HG00609.hp1 HG00733.hp1 HG01168.hp2 others(5): Show |
intron_variant | MODIFIER | c.1530+361_1530+370d others(12): Show |
LONRF3 | ENSG00000175556.17 | transcript | ENST00000371628.8 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chrX | 119006568 | |||||
| chrX:119006568
|
TTTTTG | T | 123 | a0001c0002t0001g0003a0001c0002t0001g0004a0001c0002t0001g0005others(120): Show | 134 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(131): Show |
intron_variant | MODIFIER | c.1530+366_1530+370d others(7): Show |
LONRF3 | ENSG00000175556.17 | transcript | ENST00000371628.8 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chrX | 119006568 | |||||
| chrX:119006688
|
T | C | 1 | a0001c0001t0001g0213 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.1530+453T>C | LONRF3 | ENSG00000175556.17 | transcript | ENST00000371628.8 | protein_coding | 6/10 | chrX | 119006688 | ||||||
| chrX:119006743
|
C | T | 1 | a0001c0004t0001g0258 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.1530+508C>T | LONRF3 | ENSG00000175556.17 | transcript | ENST00000371628.8 | protein_coding | 6/10 | chrX | 119006743 | ||||||
| chrX:119006831
|
A | G | 1 | a0001c0002t0001g0024 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.1530+596A>G | LONRF3 | ENSG00000175556.17 | transcript | ENST00000371628.8 | protein_coding | 6/10 | chrX | 119006831 | ||||||
| chrX:119006834
|
C | T | 1 | a0001c0002t0001g0024 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.1530+599C>T | LONRF3 | ENSG00000175556.17 | transcript | ENST00000371628.8 | protein_coding | 6/10 | chrX | 119006834 | ||||||
| chrX:119006883
|
C | T | 70 | a0001c0002t0001g0003a0001c0002t0001g0004a0001c0002t0001g0005others(67): Show | 77 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(74): Show |
intron_variant | MODIFIER | c.1530+648C>T | LONRF3 | ENSG00000175556.17 | transcript | ENST00000371628.8 | protein_coding | 6/10 | chrX | 119006883 | ||||||
| chrX:119007511
|
T | C | 2 | a0001c0002t0006g0184a0001c0002t0008g0186 | 2 | HG02630.hp1 HG02818.hp1 |
intron_variant | MODIFIER | c.1530+1276T>C | LONRF3 | ENSG00000175556.17 | transcript | ENST00000371628.8 | protein_coding | 6/10 | chrX | 119007511 | ||||||
| chrX:119007572
|
C | T | 1 | a0001c0004t0001g0279 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1530+1337C>T | LONRF3 | ENSG00000175556.17 | transcript | ENST00000371628.8 | protein_coding | 6/10 | chrX | 119007572 | ||||||
| chrX:119007732
|
T | C | 1 | a0001c0001t0002g0073 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.1531-1394T>C | LONRF3 | ENSG00000175556.17 | transcript | ENST00000371628.8 | protein_coding | 6/10 | chrX | 119007732 | ||||||
| chrX:119008130
|
T | G | 2 | a0001c0004t0001g0099a0001c0004t0001g0278 | 2 | HG02559.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.1531-996T>G | LONRF3 | ENSG00000175556.17 | transcript | ENST00000371628.8 | protein_coding | 6/10 | chrX | 119008130 | ||||||
| chrX:119008384
|
T | G | 1 | a0001c0001t0002g0082 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.1531-742T>G | LONRF3 | ENSG00000175556.17 | transcript | ENST00000371628.8 | protein_coding | 6/10 | chrX | 119008384 | ||||||
| chrX:119008661
|
C | A | 1 | a0001c0011t0003g0199 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1531-465C>A | LONRF3 | ENSG00000175556.17 | transcript | ENST00000371628.8 | protein_coding | 6/10 | chrX | 119008661 | ||||||
| chrX:119008887
|
A | AC | 1 | a0001c0001t0001g0207 | 1 | NA19006.hp1 | intron_variant | MODIFIER | c.1531-234dupC | LONRF3 | ENSG00000175556.17 | transcript | ENST00000371628.8 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chrX | 119008887 | |||||
| chrX:119008965
|
A | G | 6 | a0001c0002t0001g0144a0001c0002t0001g0145a0001c0002t0001g0146others(3): Show | 6 | HG02083.hp1 NA18941.hp2 NA18948.hp1 others(3): Show |
intron_variant | MODIFIER | c.1531-161A>G | LONRF3 | ENSG00000175556.17 | transcript | ENST00000371628.8 | protein_coding | 6/10 | chrX | 119008965 | ||||||
| chrX:119009080
|
A | G | 119 | a0001c0002t0001g0003a0001c0002t0001g0004a0001c0002t0001g0005others(116): Show | 130 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(127): Show |
intron_variant | MODIFIER | c.1531-46A>G | LONRF3 | ENSG00000175556.17 | transcript | ENST00000371628.8 | protein_coding | 6/10 | chrX | 119009080 | ||||||
| chrX:119009288
|
G | A | 2 | a0001c0001t0002g0055a0001c0001t0002g0087 | 2 | NA18968.hp2 NA18984.hp1 |
intron_variant | MODIFIER | c.1652+41G>A | LONRF3 | ENSG00000175556.17 | transcript | ENST00000371628.8 | protein_coding | 7/10 | chrX | 119009288 | ||||||
| chrX:119009568
|
G | A | 1 | a0001c0001t0001g0250 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.1652+321G>A | LONRF3 | ENSG00000175556.17 | transcript | ENST00000371628.8 | protein_coding | 7/10 | chrX | 119009568 | ||||||
| chrX:119009695
|
A | G | 1 | a0001c0011t0003g0199 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1652+448A>G | LONRF3 | ENSG00000175556.17 | transcript | ENST00000371628.8 | protein_coding | 7/10 | chrX | 119009695 | ||||||
| chrX:119009756
|
C | T | 1 | a0001c0002t0005g0028 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.1652+509C>T | LONRF3 | ENSG00000175556.17 | transcript | ENST00000371628.8 | protein_coding | 7/10 | chrX | 119009756 | ||||||
| chrX:119009780
|
CT | C | 1 | a0001c0001t0002g0113 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.1652+540delT | LONRF3 | ENSG00000175556.17 | transcript | ENST00000371628.8 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chrX | 119009780 | |||||
| chrX:119009855
|
C | T | 59 | a0001c0002t0001g0003a0001c0002t0001g0004a0001c0002t0001g0018others(56): Show | 64 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(61): Show |
intron_variant | MODIFIER | c.1652+608C>T | LONRF3 | ENSG00000175556.17 | transcript | ENST00000371628.8 | protein_coding | 7/10 | chrX | 119009855 | ||||||
| chrX:119009856
|
G | A | 1 | a0001c0004t0001g0279 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1652+609G>A | LONRF3 | ENSG00000175556.17 | transcript | ENST00000371628.8 | protein_coding | 7/10 | chrX | 119009856 | ||||||
| chrX:119009863
|
G | A | 20 | a0001c0002t0001g0008a0001c0002t0001g0009a0001c0002t0001g0029others(17): Show | 22 | HG00408.hp1 HG00423.hp1 HG00544.hp2 others(19): Show |
intron_variant | MODIFIER | c.1652+616G>A | LONRF3 | ENSG00000175556.17 | transcript | ENST00000371628.8 | protein_coding | 7/10 | chrX | 119009863 | ||||||
| chrX:119009894
|
C | T | 1 | a0001c0001t0001g0260 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.1652+647C>T | LONRF3 | ENSG00000175556.17 | transcript | ENST00000371628.8 | protein_coding | 7/10 | chrX | 119009894 | ||||||
| chrX:119010098
|
A | T | 1 | a0001c0002t0001g0160 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.1652+851A>T | LONRF3 | ENSG00000175556.17 | transcript | ENST00000371628.8 | protein_coding | 7/10 | chrX | 119010098 | ||||||
| chrX:119010155
|
CGCTTTCT | C | 2 | a0001c0004t0001g0099a0001c0004t0001g0278 | 2 | HG02559.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.1652+909_1652+915d others(9): Show |
LONRF3 | ENSG00000175556.17 | transcript | ENST00000371628.8 | protein_coding | 7/10 | chrX | 119010155 | ||||||
| chrX:119010168
|
G | A | 4 | a0001c0002t0001g0024a0001c0002t0001g0043a0001c0002t0003g0025others(1): Show | 5 | HG01891.hp1 HG02886.hp1 HG03195.hp2 others(2): Show |
intron_variant | MODIFIER | c.1652+921G>A | LONRF3 | ENSG00000175556.17 | transcript | ENST00000371628.8 | protein_coding | 7/10 | chrX | 119010168 | ||||||
| chrX:119010197
|
A | G | 20 | a0001c0002t0001g0008a0001c0002t0001g0009a0001c0002t0001g0029others(17): Show | 22 | HG00408.hp1 HG00423.hp1 HG00544.hp2 others(19): Show |
intron_variant | MODIFIER | c.1652+950A>G | LONRF3 | ENSG00000175556.17 | transcript | ENST00000371628.8 | protein_coding | 7/10 | chrX | 119010197 | ||||||
| chrX:119010208
|
C | T | 80 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0007others(77): Show | 88 | HG00280.hp1 HG00323.hp2 HG00438.hp1 others(85): Show |
intron_variant | MODIFIER | c.1652+961C>T | LONRF3 | ENSG00000175556.17 | transcript | ENST00000371628.8 | protein_coding | 7/10 | chrX | 119010208 | ||||||
| chrX:119010484
|
G | GT | 7 | a0001c0001t0001g0214a0001c0001t0002g0060a0001c0002t0001g0132others(4): Show | 7 | HG02630.hp2 HG02738.hp1 HG02895.hp1 others(4): Show |
intron_variant | MODIFIER | c.1652+1247dupT | LONRF3 | ENSG00000175556.17 | transcript | ENST00000371628.8 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chrX | 119010484 | |||||
| chrX:119010777
|
T | C | 8 | a0001c0002t0001g0185a0001c0002t0003g0187a0001c0002t0003g0188others(5): Show | 8 | HG01884.hp1 HG02622.hp1 HG02630.hp1 others(5): Show |
intron_variant | MODIFIER | c.1653-1038T>C | LONRF3 | ENSG00000175556.17 | transcript | ENST00000371628.8 | protein_coding | 7/10 | chrX | 119010777 | ||||||
| chrX:119010890
|
G | A | 1 | a0001c0001t0001g0248 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.1653-925G>A | LONRF3 | ENSG00000175556.17 | transcript | ENST00000371628.8 | protein_coding | 7/10 | chrX | 119010890 | ||||||
| chrX:119011108
|
C | T | 11 | a0001c0002t0001g0017a0001c0002t0001g0049a0001c0002t0001g0122others(8): Show | 12 | HG02055.hp1 HG02257.hp1 HG02451.hp1 others(9): Show |
intron_variant | MODIFIER | c.1653-707C>T | LONRF3 | ENSG00000175556.17 | transcript | ENST00000371628.8 | protein_coding | 7/10 | chrX | 119011108 | ||||||
| chrX:119011112
|
T | TA | 7 | a0001c0002t0001g0005a0001c0002t0001g0038a0001c0002t0001g0141others(4): Show | 9 | HG00673.hp1 HG01109.hp1 HG02109.hp1 others(6): Show |
intron_variant | MODIFIER | c.1653-686dupA | LONRF3 | ENSG00000175556.17 | transcript | ENST00000371628.8 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chrX | 119011112 | |||||
| chrX:119011112
|
TA | T | 12 | a0001c0001t0001g0224a0001c0001t0002g0072a0001c0001t0002g0106others(9): Show | 12 | HG01257.hp1 HG02559.hp1 HG02922.hp1 others(9): Show |
intron_variant | MODIFIER | c.1653-686delA | LONRF3 | ENSG00000175556.17 | transcript | ENST00000371628.8 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chrX | 119011112 | |||||
| chrX:119011280
|
T | C | 1 | a0001c0001t0001g0270 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.1653-535T>C | LONRF3 | ENSG00000175556.17 | transcript | ENST00000371628.8 | protein_coding | 7/10 | chrX | 119011280 | ||||||
| chrX:119011291
|
T | TA | 1 | a0001c0001t0001g0207 | 1 | NA19006.hp1 | intron_variant | MODIFIER | c.1653-524_1653-523i others(3): Show |
LONRF3 | ENSG00000175556.17 | transcript | ENST00000371628.8 | protein_coding | 7/10 | chrX | 119011291 | ||||||
| chrX:119011369
|
G | C | 1 | a0001c0003t0002g0031 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.1653-446G>C | LONRF3 | ENSG00000175556.17 | transcript | ENST00000371628.8 | protein_coding | 7/10 | chrX | 119011369 | ||||||
| chrX:119011457
|
G | T | 11 | a0001c0002t0001g0017a0001c0002t0001g0049a0001c0002t0001g0122others(8): Show | 12 | HG02055.hp1 HG02257.hp1 HG02451.hp1 others(9): Show |
intron_variant | MODIFIER | c.1653-358G>T | LONRF3 | ENSG00000175556.17 | transcript | ENST00000371628.8 | protein_coding | 7/10 | chrX | 119011457 | ||||||
| chrX:119011514
|
A | G | 1 | a0001c0003t0001g0174 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.1653-301A>G | LONRF3 | ENSG00000175556.17 | transcript | ENST00000371628.8 | protein_coding | 7/10 | chrX | 119011514 | ||||||
| chrX:119011748
|
A | AT | 1 | a0001c0001t0001g0207 | 1 | NA19006.hp1 | intron_variant | MODIFIER | c.1653-64dupT | LONRF3 | ENSG00000175556.17 | transcript | ENST00000371628.8 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chrX | 119011748 | |||||
| chrX:119011755
|
C | CA | 1 | a0001c0001t0001g0207 | 1 | NA19006.hp1 | intron_variant | MODIFIER | c.1653-58dupA | LONRF3 | ENSG00000175556.17 | transcript | ENST00000371628.8 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chrX | 119011755 | |||||
| chrX:119011759
|
A | AT | 1 | a0001c0001t0002g0060 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.1653-51dupT | LONRF3 | ENSG00000175556.17 | transcript | ENST00000371628.8 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chrX | 119011759 | |||||
| chrX:119012013
|
T | C | 3 | a0001c0002t0001g0154a0001c0002t0001g0156a0001c0002t0001g0160 | 3 | HG03017.hp1 HG03654.hp1 HG03710.hp1 |
intron_variant | MODIFIER | c.1811+40T>C | LONRF3 | ENSG00000175556.17 | transcript | ENST00000371628.8 | protein_coding | 8/10 | chrX | 119012013 | ||||||
| chrX:119012042
|
T | TC | 1 | a0001c0001t0001g0207 | 1 | NA19006.hp1 | intron_variant | MODIFIER | c.1811+72dupC | LONRF3 | ENSG00000175556.17 | transcript | ENST00000371628.8 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chrX | 119012042 | |||||
| chrX:119012050
|
G | A | 2 | a0001c0004t0001g0192a0001c0004t0001g0197 | 2 | HG02622.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.1811+77G>A | LONRF3 | ENSG00000175556.17 | transcript | ENST00000371628.8 | protein_coding | 8/10 | chrX | 119012050 | ||||||
| chrX:119012121
|
TG | T | 1 | a0001c0001t0001g0207 | 1 | NA19006.hp1 | intron_variant | MODIFIER | c.1811+150delG | LONRF3 | ENSG00000175556.17 | transcript | ENST00000371628.8 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chrX | 119012121 | |||||
| chrX:119012134
|
AC | A | 1 | a0001c0001t0001g0207 | 1 | NA19006.hp1 | intron_variant | MODIFIER | c.1811+163delC | LONRF3 | ENSG00000175556.17 | transcript | ENST00000371628.8 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chrX | 119012134 | |||||
| chrX:119012144
|
AG | A | 1 | a0001c0001t0001g0207 | 1 | NA19006.hp1 | intron_variant | MODIFIER | c.1811+173delG | LONRF3 | ENSG00000175556.17 | transcript | ENST00000371628.8 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chrX | 119012144 | |||||
| chrX:119012237
|
C | CT | 1 | a0001c0001t0001g0207 | 1 | NA19006.hp1 | intron_variant | MODIFIER | c.1811+265dupT | LONRF3 | ENSG00000175556.17 | transcript | ENST00000371628.8 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chrX | 119012237 | |||||
| chrX:119012375
|
G | A | 6 | a0001c0005t0001g0014a0001c0005t0001g0015a0001c0005t0001g0058others(3): Show | 8 | HG00639.hp1 HG01884.hp2 HG02572.hp1 others(5): Show |
intron_variant | MODIFIER | c.1811+402G>A | LONRF3 | ENSG00000175556.17 | transcript | ENST00000371628.8 | protein_coding | 8/10 | chrX | 119012375 | ||||||
| chrX:119012398
|
TA | T | 1 | a0001c0001t0001g0207 | 1 | NA19006.hp1 | intron_variant | MODIFIER | c.1811+429delA | LONRF3 | ENSG00000175556.17 | transcript | ENST00000371628.8 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chrX | 119012398 | |||||
| chrX:119012472
|
T | TG | 1 | a0001c0001t0001g0207 | 1 | NA19006.hp1 | intron_variant | MODIFIER | c.1811+499_1811+500i others(3): Show |
LONRF3 | ENSG00000175556.17 | transcript | ENST00000371628.8 | protein_coding | 8/10 | chrX | 119012472 | ||||||
| chrX:119012513
|
TG | T | 1 | a0001c0001t0001g0207 | 1 | NA19006.hp1 | intron_variant | MODIFIER | c.1812-523delG | LONRF3 | ENSG00000175556.17 | transcript | ENST00000371628.8 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chrX | 119012513 | |||||
| chrX:119012618
|
A | G | 1 | a0001c0002t0001g0169 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.1812-421A>G | LONRF3 | ENSG00000175556.17 | transcript | ENST00000371628.8 | protein_coding | 8/10 | chrX | 119012618 | ||||||
| chrX:119012635
|
C | CT | 1 | a0001c0001t0001g0207 | 1 | NA19006.hp1 | intron_variant | MODIFIER | c.1812-400dupT | LONRF3 | ENSG00000175556.17 | transcript | ENST00000371628.8 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chrX | 119012635 | |||||
| chrX:119012847
|
C | T | 80 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0007others(77): Show | 88 | HG00280.hp1 HG00323.hp2 HG00438.hp1 others(85): Show |
intron_variant | MODIFIER | c.1812-192C>T | LONRF3 | ENSG00000175556.17 | transcript | ENST00000371628.8 | protein_coding | 8/10 | chrX | 119012847 | ||||||
| chrX:119012861
|
A | AT | 1 | a0005c0010t0007g0176 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.1812-170dupT | LONRF3 | ENSG00000175556.17 | transcript | ENST00000371628.8 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chrX | 119012861 | |||||
| chrX:119012861
|
AT | A | 1 | a0001c0001t0001g0207 | 1 | NA19006.hp1 | intron_variant | MODIFIER | c.1812-170delT | LONRF3 | ENSG00000175556.17 | transcript | ENST00000371628.8 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chrX | 119012861 | |||||
| chrX:119012925
|
A | G | 1 | a0002c0006t0001g0265 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.1812-114A>G | LONRF3 | ENSG00000175556.17 | transcript | ENST00000371628.8 | protein_coding | 8/10 | chrX | 119012925 | ||||||
| chrX:119012979
|
A | AG | 1 | a0001c0001t0001g0207 | 1 | NA19006.hp1 | intron_variant | MODIFIER | c.1812-59dupG | LONRF3 | ENSG00000175556.17 | transcript | ENST00000371628.8 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chrX | 119012979 | |||||
| chrX:119013270
|
G | T | 107 | a0001c0002t0001g0003a0001c0002t0001g0004a0001c0002t0001g0005others(104): Show | 117 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(114): Show |
intron_variant | MODIFIER | c.1974+69G>T | LONRF3 | ENSG00000175556.17 | transcript | ENST00000371628.8 | protein_coding | 9/10 | chrX | 119013270 | ||||||
| chrX:119013502
|
G | A | 119 | a0001c0002t0001g0003a0001c0002t0001g0004a0001c0002t0001g0005others(116): Show | 130 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(127): Show |
intron_variant | MODIFIER | c.1974+301G>A | LONRF3 | ENSG00000175556.17 | transcript | ENST00000371628.8 | protein_coding | 9/10 | chrX | 119013502 | ||||||
| chrX:119013655
|
C | A | 205 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0007others(202): Show | 224 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(221): Show |
intron_variant | MODIFIER | c.1974+454C>A | LONRF3 | ENSG00000175556.17 | transcript | ENST00000371628.8 | protein_coding | 9/10 | chrX | 119013655 | ||||||
| chrX:119013738
|
AT | A | 1 | a0001c0001t0001g0026 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.1975-466delT | LONRF3 | ENSG00000175556.17 | transcript | ENST00000371628.8 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chrX | 119013738 | |||||
| chrX:119013838
|
G | A | 1 | a0001c0002t0001g0034 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.1975-369G>A | LONRF3 | ENSG00000175556.17 | transcript | ENST00000371628.8 | protein_coding | 9/10 | chrX | 119013838 | ||||||
| chrX:119013891
|
G | A | 1 | a0001c0004t0001g0211 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.1975-316G>A | LONRF3 | ENSG00000175556.17 | transcript | ENST00000371628.8 | protein_coding | 9/10 | chrX | 119013891 | ||||||
| chrX:119013893
|
C | G | 1 | a0001c0001t0002g0074 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.1975-314C>G | LONRF3 | ENSG00000175556.17 | transcript | ENST00000371628.8 | protein_coding | 9/10 | chrX | 119013893 | ||||||
| chrX:119013961
|
C | T | 9 | a0001c0002t0001g0005a0001c0002t0001g0022a0001c0002t0001g0161others(6): Show | 11 | HG01109.hp1 HG01243.hp1 HG02109.hp1 others(8): Show |
intron_variant | MODIFIER | c.1975-246C>T | LONRF3 | ENSG00000175556.17 | transcript | ENST00000371628.8 | protein_coding | 9/10 | chrX | 119013961 | ||||||
| chrX:119014003
|
T | TC | 1 | a0004c0008t0001g0256 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.1975-202dupC | LONRF3 | ENSG00000175556.17 | transcript | ENST00000371628.8 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chrX | 119014003 | |||||
| chrX:119014058
|
A | AT | 1 | a0004c0008t0001g0256 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.1975-146dupT | LONRF3 | ENSG00000175556.17 | transcript | ENST00000371628.8 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chrX | 119014058 | |||||
| chrX:119014104
|
T | C | 1 | a0001c0004t0001g0095 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1975-103T>C | LONRF3 | ENSG00000175556.17 | transcript | ENST00000371628.8 | protein_coding | 9/10 | chrX | 119014104 | ||||||
| chrX:119014473
|
G | A | 1 | a0001c0002t0001g0156 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.2124+117G>A | LONRF3 | ENSG00000175556.17 | transcript | ENST00000371628.8 | protein_coding | 10/10 | chrX | 119014473 | ||||||
| chrX:119014482
|
T | TG | 1 | a0004c0008t0001g0256 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.2124+128dupG | LONRF3 | ENSG00000175556.17 | transcript | ENST00000371628.8 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chrX | 119014482 | |||||
| chrX:119014494
|
G | GT | 1 | a0004c0008t0001g0256 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.2124+138_2124+139i others(3): Show |
LONRF3 | ENSG00000175556.17 | transcript | ENST00000371628.8 | protein_coding | 10/10 | chrX | 119014494 | ||||||
| chrX:119014544
|
C | CG | 1 | a0004c0008t0001g0256 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.2124+192dupG | LONRF3 | ENSG00000175556.17 | transcript | ENST00000371628.8 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chrX | 119014544 | |||||
| chrX:119014631
|
C | CA | 1 | a0004c0008t0001g0256 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.2124+276dupA | LONRF3 | ENSG00000175556.17 | transcript | ENST00000371628.8 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chrX | 119014631 | |||||
| chrX:119014659
|
C | T | 11 | a0001c0002t0001g0017a0001c0002t0001g0049a0001c0002t0001g0122others(8): Show | 12 | HG02055.hp1 HG02257.hp1 HG02451.hp1 others(9): Show |
intron_variant | MODIFIER | c.2124+303C>T | LONRF3 | ENSG00000175556.17 | transcript | ENST00000371628.8 | protein_coding | 10/10 | chrX | 119014659 | ||||||
| chrX:119014744
|
C | CA | 1 | a0004c0008t0001g0256 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.2124+392dupA | LONRF3 | ENSG00000175556.17 | transcript | ENST00000371628.8 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chrX | 119014744 | |||||
| chrX:119014780
|
TC | T | 1 | a0004c0008t0001g0256 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.2124+427delC | LONRF3 | ENSG00000175556.17 | transcript | ENST00000371628.8 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chrX | 119014780 | |||||
| chrX:119014818
|
A | AC | 1 | a0004c0008t0001g0256 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.2124+465dupC | LONRF3 | ENSG00000175556.17 | transcript | ENST00000371628.8 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chrX | 119014818 | |||||
| chrX:119015168
|
G | C | 206 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0007others(203): Show | 225 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(222): Show |
intron_variant | MODIFIER | c.2124+812G>C | LONRF3 | ENSG00000175556.17 | transcript | ENST00000371628.8 | protein_coding | 10/10 | chrX | 119015168 | ||||||
| chrX:119015227
|
T | TC | 1 | a0005c0010t0007g0176 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.2124+875dupC | LONRF3 | ENSG00000175556.17 | transcript | ENST00000371628.8 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chrX | 119015227 | |||||
| chrX:119015235
|
T | C | 102 | a0001c0002t0001g0003a0001c0002t0001g0004a0001c0002t0001g0005others(99): Show | 111 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(108): Show |
intron_variant | MODIFIER | c.2124+879T>C | LONRF3 | ENSG00000175556.17 | transcript | ENST00000371628.8 | protein_coding | 10/10 | chrX | 119015235 | ||||||
| chrX:119015279
|
A | AG | 1 | a0004c0008t0001g0256 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.2124+924dupG | LONRF3 | ENSG00000175556.17 | transcript | ENST00000371628.8 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chrX | 119015279 | |||||
| chrX:119015306
|
G | A | 108 | a0001c0002t0001g0003a0001c0002t0001g0004a0001c0002t0001g0005others(105): Show | 118 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(115): Show |
intron_variant | MODIFIER | c.2124+950G>A | LONRF3 | ENSG00000175556.17 | transcript | ENST00000371628.8 | protein_coding | 10/10 | chrX | 119015306 | ||||||
| chrX:119015329
|
T | TC | 1 | a0005c0010t0007g0176 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.2124+976dupC | LONRF3 | ENSG00000175556.17 | transcript | ENST00000371628.8 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chrX | 119015329 | |||||
| chrX:119015369
|
G | GT | 1 | a0004c0008t0001g0256 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.2124+1015dupT | LONRF3 | ENSG00000175556.17 | transcript | ENST00000371628.8 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chrX | 119015369 | |||||
| chrX:119015403
|
G | A | 102 | a0001c0002t0001g0003a0001c0002t0001g0004a0001c0002t0001g0005others(99): Show | 111 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(108): Show |
intron_variant | MODIFIER | c.2124+1047G>A | LONRF3 | ENSG00000175556.17 | transcript | ENST00000371628.8 | protein_coding | 10/10 | chrX | 119015403 | ||||||
| chrX:119015423
|
TC | T | 1 | a0005c0010t0007g0176 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.2124+1070delC | LONRF3 | ENSG00000175556.17 | transcript | ENST00000371628.8 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chrX | 119015423 | |||||
| chrX:119015437
|
G | A | 1 | a0001c0003t0001g0178 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.2124+1081G>A | LONRF3 | ENSG00000175556.17 | transcript | ENST00000371628.8 | protein_coding | 10/10 | chrX | 119015437 | ||||||
| chrX:119015476
|
C | A | 5 | a0001c0002t0001g0023a0001c0002t0001g0024a0001c0002t0001g0043others(2): Show | 6 | HG01106.hp1 HG01891.hp1 HG02886.hp1 others(3): Show |
intron_variant | MODIFIER | c.2124+1120C>A | LONRF3 | ENSG00000175556.17 | transcript | ENST00000371628.8 | protein_coding | 10/10 | chrX | 119015476 | ||||||
| chrX:119015552
|
G | A | 1 | a0001c0001t0002g0110 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.2124+1196G>A | LONRF3 | ENSG00000175556.17 | transcript | ENST00000371628.8 | protein_coding | 10/10 | chrX | 119015552 | ||||||
| chrX:119015567
|
A | AG | 1 | a0005c0010t0007g0176 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.2124+1213dupG | LONRF3 | ENSG00000175556.17 | transcript | ENST00000371628.8 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chrX | 119015567 | |||||
| chrX:119015615
|
TC | T | 1 | a0001c0002t0005g0028 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.2124+1263delC | LONRF3 | ENSG00000175556.17 | transcript | ENST00000371628.8 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chrX | 119015615 | |||||
| chrX:119015623
|
AC | A | 1 | a0005c0010t0007g0176 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.2124+1269delC | LONRF3 | ENSG00000175556.17 | transcript | ENST00000371628.8 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chrX | 119015623 | |||||
| chrX:119015662
|
A | G | 1 | a0001c0002t0005g0028 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.2124+1306A>G | LONRF3 | ENSG00000175556.17 | transcript | ENST00000371628.8 | protein_coding | 10/10 | chrX | 119015662 | ||||||
| chrX:119015673
|
TA | T | 1 | a0005c0010t0007g0176 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.2124+1319delA | LONRF3 | ENSG00000175556.17 | transcript | ENST00000371628.8 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chrX | 119015673 | |||||
| chrX:119015724
|
GA | G | 1 | a0005c0010t0007g0176 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.2124+1371delA | LONRF3 | ENSG00000175556.17 | transcript | ENST00000371628.8 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chrX | 119015724 | |||||
| chrX:119015807
|
GA | G | 1 | a0005c0010t0007g0176 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.2124+1456delA | LONRF3 | ENSG00000175556.17 | transcript | ENST00000371628.8 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chrX | 119015807 | |||||
| chrX:119015840
|
CA | C | 1 | a0005c0010t0007g0176 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.2124+1486delA | LONRF3 | ENSG00000175556.17 | transcript | ENST00000371628.8 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chrX | 119015840 | |||||
| chrX:119015860
|
T | TC | 1 | a0005c0010t0007g0176 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.2124+1507dupC | LONRF3 | ENSG00000175556.17 | transcript | ENST00000371628.8 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chrX | 119015860 | |||||
| chrX:119015951
|
TG | T | 1 | a0005c0010t0007g0176 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.2125-1582delG | LONRF3 | ENSG00000175556.17 | transcript | ENST00000371628.8 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chrX | 119015951 | |||||
| chrX:119016026
|
G | A | 1 | a0005c0010t0007g0176 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.2125-1509G>A | LONRF3 | ENSG00000175556.17 | transcript | ENST00000371628.8 | protein_coding | 10/10 | chrX | 119016026 | ||||||
| chrX:119016027
|
A | G | 1 | a0005c0010t0007g0176 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.2125-1508A>G | LONRF3 | ENSG00000175556.17 | transcript | ENST00000371628.8 | protein_coding | 10/10 | chrX | 119016027 | ||||||
| chrX:119016053
|
T | C | 119 | a0001c0002t0001g0003a0001c0002t0001g0004a0001c0002t0001g0005others(116): Show | 130 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(127): Show |
intron_variant | MODIFIER | c.2125-1482T>C | LONRF3 | ENSG00000175556.17 | transcript | ENST00000371628.8 | protein_coding | 10/10 | chrX | 119016053 | ||||||
| chrX:119016062
|
CA | C | 1 | a0005c0010t0007g0176 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.2125-1470delA | LONRF3 | ENSG00000175556.17 | transcript | ENST00000371628.8 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chrX | 119016062 | |||||
| chrX:119016095
|
C | T | 18 | a0001c0002t0001g0008a0001c0002t0001g0009a0001c0002t0001g0029others(15): Show | 20 | HG00408.hp1 HG00423.hp1 HG00544.hp2 others(17): Show |
intron_variant | MODIFIER | c.2125-1440C>T | LONRF3 | ENSG00000175556.17 | transcript | ENST00000371628.8 | protein_coding | 10/10 | chrX | 119016095 | ||||||
| chrX:119016258
|
A | G | 1 | a0001c0001t0001g0249 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.2125-1277A>G | LONRF3 | ENSG00000175556.17 | transcript | ENST00000371628.8 | protein_coding | 10/10 | chrX | 119016258 | ||||||
| chrX:119016274
|
G | C | 2 | a0001c0001t0002g0057a0001c0001t0002g0104 | 2 | HG01928.hp1 HG01978.hp1 |
intron_variant | MODIFIER | c.2125-1261G>C | LONRF3 | ENSG00000175556.17 | transcript | ENST00000371628.8 | protein_coding | 10/10 | chrX | 119016274 | ||||||
| chrX:119016317
|
AG | A | 1 | a0001c0001t0001g0207 | 1 | NA19006.hp1 | intron_variant | MODIFIER | c.2125-1214delG | LONRF3 | ENSG00000175556.17 | transcript | ENST00000371628.8 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chrX | 119016317 | |||||
| chrX:119016330
|
A | ATTTC | 63 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0020others(60): Show | 69 | HG00280.hp1 HG00323.hp2 HG00438.hp1 others(66): Show |
intron_variant | MODIFIER | c.2125-1185_2125-118 others(8): Show |
LONRF3 | ENSG00000175556.17 | transcript | ENST00000371628.8 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chrX | 119016330 | |||||
| chrX:119016330
|
A | ATTTCTTT others(1): Show |
16 | a0001c0001t0001g0007a0001c0001t0001g0026a0001c0001t0001g0027others(13): Show | 18 | HG00544.hp1 HG00597.hp1 HG01346.hp2 others(15): Show |
intron_variant | MODIFIER | c.2125-1189_2125-118 others(12): Show |
LONRF3 | ENSG00000175556.17 | transcript | ENST00000371628.8 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chrX | 119016330 | |||||
| chrX:119016350
|
C | CT | 100 | a0001c0001t0001g0112a0001c0001t0002g0072a0001c0002t0001g0003others(97): Show | 110 | HG00099.hp1 HG00323.hp1 HG00408.hp1 others(107): Show |
intron_variant | MODIFIER | c.2125-1169dupT | LONRF3 | ENSG00000175556.17 | transcript | ENST00000371628.8 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chrX | 119016350 | |||||
| chrX:119016350
|
C | CTT | 16 | a0001c0002t0001g0023a0001c0002t0001g0024a0001c0002t0001g0029others(13): Show | 17 | HG00140.hp1 HG01106.hp1 HG01884.hp1 others(14): Show |
intron_variant | MODIFIER | c.2125-1170_2125-116 others(6): Show |
LONRF3 | ENSG00000175556.17 | transcript | ENST00000371628.8 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chrX | 119016350 | |||||
| chrX:119016350
|
C | CTTTCT | 2 | a0001c0001t0001g0235a0004c0008t0001g0256 | 2 | NA19083.hp1 NA19087.hp2 |
intron_variant | MODIFIER | c.2125-1182_2125-118 others(9): Show |
LONRF3 | ENSG00000175556.17 | transcript | ENST00000371628.8 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chrX | 119016350 | |||||
| chrX:119016350
|
CT | C | 3 | a0001c0001t0002g0055a0001c0001t0002g0071a0001c0003t0001g0171 | 3 | HG01256.hp1 NA18982.hp1 NA18984.hp1 |
intron_variant | MODIFIER | c.2125-1169delT | LONRF3 | ENSG00000175556.17 | transcript | ENST00000371628.8 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chrX | 119016350 | |||||
| chrX:119016501
|
C | A | 1 | a0001c0002t0005g0028 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.2125-1034C>A | LONRF3 | ENSG00000175556.17 | transcript | ENST00000371628.8 | protein_coding | 10/10 | chrX | 119016501 | ||||||
| chrX:119016502
|
C | T | 1 | a0001c0001t0001g0234 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.2125-1033C>T | LONRF3 | ENSG00000175556.17 | transcript | ENST00000371628.8 | protein_coding | 10/10 | chrX | 119016502 | ||||||
| chrX:119016503
|
G | T | 6 | a0001c0002t0001g0009a0001c0002t0001g0029a0001c0002t0001g0032others(3): Show | 7 | NA18956.hp1 NA18960.hp1 NA18967.hp1 others(4): Show |
intron_variant | MODIFIER | c.2125-1032G>T | LONRF3 | ENSG00000175556.17 | transcript | ENST00000371628.8 | protein_coding | 10/10 | chrX | 119016503 | ||||||
| chrX:119016504
|
C | A | 90 | a0001c0002t0001g0003a0001c0002t0001g0004a0001c0002t0001g0005others(87): Show | 99 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(96): Show |
intron_variant | MODIFIER | c.2125-1031C>A | LONRF3 | ENSG00000175556.17 | transcript | ENST00000371628.8 | protein_coding | 10/10 | chrX | 119016504 | ||||||
| chrX:119016537
|
T | TG | 1 | a0004c0008t0001g0256 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.2125-994dupG | LONRF3 | ENSG00000175556.17 | transcript | ENST00000371628.8 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chrX | 119016537 | |||||
| chrX:119016671
|
A | C | 1 | a0005c0010t0007g0176 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.2125-864A>C | LONRF3 | ENSG00000175556.17 | transcript | ENST00000371628.8 | protein_coding | 10/10 | chrX | 119016671 | ||||||
| chrX:119016695
|
C | A | 5 | a0001c0002t0001g0023a0001c0002t0001g0024a0001c0002t0001g0043others(2): Show | 6 | HG01106.hp1 HG01891.hp1 HG02886.hp1 others(3): Show |
intron_variant | MODIFIER | c.2125-840C>A | LONRF3 | ENSG00000175556.17 | transcript | ENST00000371628.8 | protein_coding | 10/10 | chrX | 119016695 | ||||||
| chrX:119016704
|
A | G | 206 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0007others(203): Show | 225 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(222): Show |
intron_variant | MODIFIER | c.2125-831A>G | LONRF3 | ENSG00000175556.17 | transcript | ENST00000371628.8 | protein_coding | 10/10 | chrX | 119016704 | ||||||
| chrX:119016751
|
GA | G | 1 | a0005c0010t0007g0176 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.2125-782delA | LONRF3 | ENSG00000175556.17 | transcript | ENST00000371628.8 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chrX | 119016751 | |||||
| chrX:119017062
|
T | TG | 1 | a0005c0010t0007g0176 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.2125-471dupG | LONRF3 | ENSG00000175556.17 | transcript | ENST00000371628.8 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chrX | 119017062 | |||||
| chrX:119017181
|
C | T | 1 | a0001c0001t0001g0260 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.2125-354C>T | LONRF3 | ENSG00000175556.17 | transcript | ENST00000371628.8 | protein_coding | 10/10 | chrX | 119017181 | ||||||
| chrX:119017187
|
G | A | 1 | a0001c0002t0001g0135 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.2125-348G>A | LONRF3 | ENSG00000175556.17 | transcript | ENST00000371628.8 | protein_coding | 10/10 | chrX | 119017187 | ||||||
| chrX:119017304
|
GA | G | 1 | a0005c0010t0007g0176 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.2125-229delA | LONRF3 | ENSG00000175556.17 | transcript | ENST00000371628.8 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chrX | 119017304 | |||||
| chrX:119017497
|
TG | T | 1 | a0005c0010t0007g0176 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.2125-35delG | LONRF3 | ENSG00000175556.17 | transcript | ENST00000371628.8 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chrX | 119017497 |