Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| geneid | 1741 |
|---|---|
| ensemblid | ENSG00000082458.12 |
| hgncid | 2902 |
| symbol | DLG3 |
| name | discs large MAGUK scaffold protein 3 |
| refseq_nuc | NM_021120.4 |
| refseq_prot | NP_066943.2 |
| ensembl_nuc | ENST00000374360.8 |
| ensembl_prot | ENSP00000363480.3 |
| mane_status | MANE Select |
| chr | chrX |
| start | 70444835 |
| end | 70505490 |
| strand | + |
| ver | v1.2 |
| region | chrX:70444835-70505490 |
| region5000 | chrX:70439835-70510490 |
| regionname0 | DLG3_chrX_70444835_70505490 |
| regionname5000 | DLG3_chrX_70439835_70510490 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 817 | 271 | 70 | 43 | 115 | 11 | 30 | 92 | DLG3_chrX_70439835_70510490 | DLG3 | copy fasta | chrX | 70439835 | 70510490 |
| a0002 | 0/0 | 86 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | DLG3_chrX_70439835_70510490 | DLG3 | copy fasta | chrX | 70439835 | 70510490 |
| a0003 | 0/0 | 817 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | DLG3_chrX_70439835_70510490 | DLG3 | copy fasta | chrX | 70439835 | 70510490 |
| a0004 | 0/0 | 335 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | DLG3_chrX_70439835_70510490 | DLG3 | copy fasta | chrX | 70439835 | 70510490 |
| a0005 | 0/0 | 420 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | DLG3_chrX_70439835_70510490 | DLG3 | copy fasta | chrX | 70439835 | 70510490 |
| a0006 | 0/0 | 420 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | DLG3_chrX_70439835_70510490 | DLG3 | copy fasta | chrX | 70439835 | 70510490 |
| a0007 | 0/0 | 87 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | DLG3_chrX_70439835_70510490 | DLG3 | copy fasta | chrX | 70439835 | 70510490 |
| a0008 | 0/0 | 284 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | DLG3_chrX_70439835_70510490 | DLG3 | copy fasta | chrX | 70439835 | 70510490 |
| chapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| c0001 | 1/1 | 2454 | 264 | 66 | 41 | 114 | 11 | 30 | DLG3_chrX_70439835_70510490 | DLG3 | copy fasta | chrX | 70439835 | 70510490 |
| c0002 | 0/0 | 2454 | 6 | 4 | 2 | 0 | 0 | 0 | DLG3_chrX_70439835_70510490 | DLG3 | copy fasta | chrX | 70439835 | 70510490 |
| c0003 | 0/0 | 2453 | 1 | 0 | 0 | 1 | 0 | 0 | DLG3_chrX_70439835_70510490 | DLG3 | copy fasta | chrX | 70439835 | 70510490 |
| c0004 | 0/0 | 2455 | 1 | 0 | 0 | 1 | 0 | 0 | DLG3_chrX_70439835_70510490 | DLG3 | copy fasta | chrX | 70439835 | 70510490 |
| c0005 | 0/0 | 2459 | 1 | 0 | 0 | 1 | 0 | 0 | DLG3_chrX_70439835_70510490 | DLG3 | copy fasta | chrX | 70439835 | 70510490 |
| c0006 | 0/0 | 2456 | 1 | 0 | 0 | 1 | 0 | 0 | DLG3_chrX_70439835_70510490 | DLG3 | copy fasta | chrX | 70439835 | 70510490 |
| c0007 | 0/0 | 2454 | 1 | 0 | 0 | 1 | 0 | 0 | DLG3_chrX_70439835_70510490 | DLG3 | copy fasta | chrX | 70439835 | 70510490 |
| c0008 | 0/0 | 2455 | 1 | 0 | 0 | 1 | 0 | 0 | DLG3_chrX_70439835_70510490 | DLG3 | copy fasta | chrX | 70439835 | 70510490 |
| c0009 | 0/0 | 2454 | 1 | 0 | 1 | 0 | 0 | 0 | DLG3_chrX_70439835_70510490 | DLG3 | copy fasta | chrX | 70439835 | 70510490 |
| c0010 | 0/0 | 2465 | 1 | 0 | 0 | 1 | 0 | 0 | DLG3_chrX_70439835_70510490 | DLG3 | copy fasta | chrX | 70439835 | 70510490 |
| thapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| t0001 | 0/0 | 3589 | 106 | 38 | 13 | 46 | 3 | 6 | DLG3_chrX_70439835_70510490 | DLG3 | copy fasta | chrX | 70439835 | 70510490 |
| t0002 | 1/0 | 3589 | 101 | 5 | 15 | 63 | 6 | 11 | DLG3_chrX_70439835_70510490 | DLG3 | copy fasta | chrX | 70439835 | 70510490 |
| t0003 | 0/0 | 3589 | 12 | 1 | 6 | 0 | 1 | 4 | DLG3_chrX_70439835_70510490 | DLG3 | copy fasta | chrX | 70439835 | 70510490 |
| t0004 | 0/0 | 3589 | 7 | 7 | 0 | 0 | 0 | 0 | DLG3_chrX_70439835_70510490 | DLG3 | copy fasta | chrX | 70439835 | 70510490 |
| t0005 | 0/0 | 3590 | 7 | 5 | 2 | 0 | 0 | 0 | DLG3_chrX_70439835_70510490 | DLG3 | copy fasta | chrX | 70439835 | 70510490 |
| t0006 | 0/0 | 3590 | 5 | 0 | 0 | 3 | 0 | 2 | DLG3_chrX_70439835_70510490 | DLG3 | copy fasta | chrX | 70439835 | 70510490 |
| t0007 | 0/0 | 3595 | 4 | 4 | 0 | 0 | 0 | 0 | DLG3_chrX_70439835_70510490 | DLG3 | copy fasta | chrX | 70439835 | 70510490 |
| t0008 | 0/0 | 3588 | 4 | 0 | 0 | 4 | 0 | 0 | DLG3_chrX_70439835_70510490 | DLG3 | copy fasta | chrX | 70439835 | 70510490 |
| t0009 | 0/0 | 3577 | 4 | 0 | 4 | 0 | 0 | 0 | DLG3_chrX_70439835_70510490 | DLG3 | copy fasta | chrX | 70439835 | 70510490 |
| t0010 | 0/0 | 3590 | 3 | 0 | 1 | 0 | 0 | 2 | DLG3_chrX_70439835_70510490 | DLG3 | copy fasta | chrX | 70439835 | 70510490 |
| t0011 | 0/0 | 3589 | 3 | 3 | 0 | 0 | 0 | 0 | DLG3_chrX_70439835_70510490 | DLG3 | copy fasta | chrX | 70439835 | 70510490 |
| t0012 | 0/1 | 3589 | 3 | 0 | 1 | 0 | 1 | 0 | DLG3_chrX_70439835_70510490 | DLG3 | copy fasta | chrX | 70439835 | 70510490 |
| t0013 | 0/0 | 3592 | 1 | 0 | 0 | 1 | 0 | 0 | DLG3_chrX_70439835_70510490 | DLG3 | copy fasta | chrX | 70439835 | 70510490 |
| t0014 | 0/0 | 3590 | 1 | 0 | 0 | 0 | 0 | 1 | DLG3_chrX_70439835_70510490 | DLG3 | copy fasta | chrX | 70439835 | 70510490 |
| t0015 | 0/0 | 3590 | 1 | 0 | 0 | 1 | 0 | 0 | DLG3_chrX_70439835_70510490 | DLG3 | copy fasta | chrX | 70439835 | 70510490 |
| t0016 | 0/0 | 3589 | 1 | 0 | 0 | 0 | 0 | 1 | DLG3_chrX_70439835_70510490 | DLG3 | copy fasta | chrX | 70439835 | 70510490 |
| t0017 | 0/0 | 3590 | 1 | 0 | 1 | 0 | 0 | 0 | DLG3_chrX_70439835_70510490 | DLG3 | copy fasta | chrX | 70439835 | 70510490 |
| t0018 | 0/0 | 3589 | 1 | 0 | 0 | 1 | 0 | 0 | DLG3_chrX_70439835_70510490 | DLG3 | copy fasta | chrX | 70439835 | 70510490 |
| t0019 | 0/0 | 3591 | 1 | 1 | 0 | 0 | 0 | 0 | DLG3_chrX_70439835_70510490 | DLG3 | copy fasta | chrX | 70439835 | 70510490 |
| t0020 | 0/0 | 3587 | 1 | 1 | 0 | 0 | 0 | 0 | DLG3_chrX_70439835_70510490 | DLG3 | copy fasta | chrX | 70439835 | 70510490 |
| t0021 | 0/0 | 3589 | 1 | 0 | 0 | 1 | 0 | 0 | DLG3_chrX_70439835_70510490 | DLG3 | copy fasta | chrX | 70439835 | 70510490 |
| t0022 | 0/0 | 3589 | 1 | 1 | 0 | 0 | 0 | 0 | DLG3_chrX_70439835_70510490 | DLG3 | copy fasta | chrX | 70439835 | 70510490 |
| t0023 | 0/0 | 3589 | 1 | 0 | 0 | 0 | 0 | 1 | DLG3_chrX_70439835_70510490 | DLG3 | copy fasta | chrX | 70439835 | 70510490 |
| t0024 | 0/0 | 3589 | 1 | 0 | 1 | 0 | 0 | 0 | DLG3_chrX_70439835_70510490 | DLG3 | copy fasta | chrX | 70439835 | 70510490 |
| t0025 | 0/0 | 3589 | 1 | 1 | 0 | 0 | 0 | 0 | DLG3_chrX_70439835_70510490 | DLG3 | copy fasta | chrX | 70439835 | 70510490 |
| t0026 | 0/0 | 3590 | 1 | 0 | 0 | 0 | 0 | 1 | DLG3_chrX_70439835_70510490 | DLG3 | copy fasta | chrX | 70439835 | 70510490 |
| t0027 | 0/0 | 3590 | 1 | 1 | 0 | 0 | 0 | 0 | DLG3_chrX_70439835_70510490 | DLG3 | copy fasta | chrX | 70439835 | 70510490 |
| t0028 | 0/0 | 3591 | 1 | 1 | 0 | 0 | 0 | 0 | DLG3_chrX_70439835_70510490 | DLG3 | copy fasta | chrX | 70439835 | 70510490 |
| t0029 | 0/0 | 3587 | 1 | 1 | 0 | 0 | 0 | 0 | DLG3_chrX_70439835_70510490 | DLG3 | copy fasta | chrX | 70439835 | 70510490 |
| t0030 | 0/0 | 3590 | 1 | 0 | 0 | 0 | 0 | 1 | DLG3_chrX_70439835_70510490 | DLG3 | copy fasta | chrX | 70439835 | 70510490 |
| t0031 | 0/0 | 3597 | 1 | 0 | 0 | 1 | 0 | 0 | DLG3_chrX_70439835_70510490 | DLG3 | copy fasta | chrX | 70439835 | 70510490 |
| ghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| g0001 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| g0002 | 0/0 | 5 | 0 | 2 | 2 | 0 | 1 | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| g0003 | 1/0 | 4 | 3 | 0 | 0 | 0 | 0 | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| g0004 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| g0005 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| g0006 | 0/1 | 3 | 0 | 1 | 0 | 1 | 0 | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| g0007 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| g0008 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| g0009 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| g0010 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| g0011 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| g0012 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| g0013 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| g0014 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| g0015 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| g0016 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| g0017 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| g0018 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| g0028 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| g0030 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| g0031 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| g0032 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| g0033 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| g0034 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| g0035 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| g0036 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| g0038 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| g0052 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| g0053 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| g0055 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| g0060 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| g0062 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| g0064 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| g0066 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| g0067 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| g0069 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| g0074 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| g0080 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| g0081 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| g0083 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| g0090 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| g0094 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| g0098 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| g0100 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| g0102 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| g0105 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| g0106 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| g0107 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| g0109 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| g0110 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| g0114 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| g0117 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| g0125 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| g0133 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| g0134 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| g0136 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| g0138 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| g0140 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| g0143 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| g0144 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| g0145 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| g0147 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| g0154 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| g0156 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| g0164 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| g0165 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| g0173 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| g0176 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| g0177 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| g0179 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| g0180 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| g0183 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| g0184 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| g0185 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| g0186 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| g0202 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| g0203 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| g0207 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| g0210 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| g0211 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| g0215 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| g0216 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| g0217 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| g0219 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| g0248 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| achapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 2454 | 264 | 66 | 41 | 114 | 11 | 30 | DLG3_chrX_70439835_70510490 | DLG3 | copy fasta | chrX | 70439835 | 70510490 |
| a0001c0002 | 0/0 | 2454 | 6 | 4 | 2 | 0 | 0 | 0 | DLG3_chrX_70439835_70510490 | DLG3 | copy fasta | chrX | 70439835 | 70510490 |
| a0001c0007 | 0/0 | 2454 | 1 | 0 | 0 | 1 | 0 | 0 | DLG3_chrX_70439835_70510490 | DLG3 | copy fasta | chrX | 70439835 | 70510490 |
| a0002c0003 | 0/0 | 2453 | 1 | 0 | 0 | 1 | 0 | 0 | DLG3_chrX_70439835_70510490 | DLG3 | copy fasta | chrX | 70439835 | 70510490 |
| a0003c0009 | 0/0 | 2454 | 1 | 0 | 1 | 0 | 0 | 0 | DLG3_chrX_70439835_70510490 | DLG3 | copy fasta | chrX | 70439835 | 70510490 |
| a0004c0005 | 0/0 | 2459 | 1 | 0 | 0 | 1 | 0 | 0 | DLG3_chrX_70439835_70510490 | DLG3 | copy fasta | chrX | 70439835 | 70510490 |
| a0005c0008 | 0/0 | 2455 | 1 | 0 | 0 | 1 | 0 | 0 | DLG3_chrX_70439835_70510490 | DLG3 | copy fasta | chrX | 70439835 | 70510490 |
| a0006c0006 | 0/0 | 2456 | 1 | 0 | 0 | 1 | 0 | 0 | DLG3_chrX_70439835_70510490 | DLG3 | copy fasta | chrX | 70439835 | 70510490 |
| a0007c0004 | 0/0 | 2455 | 1 | 0 | 0 | 1 | 0 | 0 | DLG3_chrX_70439835_70510490 | DLG3 | copy fasta | chrX | 70439835 | 70510490 |
| a0008c0010 | 0/0 | 2465 | 1 | 0 | 0 | 1 | 0 | 0 | DLG3_chrX_70439835_70510490 | DLG3 | copy fasta | chrX | 70439835 | 70510490 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/0 | 6042 | 104 | 38 | 13 | 44 | 3 | 6 | DLG3_chrX_70439835_70510490 | DLG3 | copy fasta | chrX | 70439835 | 70510490 |
| a0001c0001t0002 | 1/0 | 6042 | 97 | 5 | 14 | 60 | 6 | 11 | DLG3_chrX_70439835_70510490 | DLG3 | copy fasta | chrX | 70439835 | 70510490 |
| a0001c0001t0003 | 0/0 | 6042 | 12 | 1 | 6 | 0 | 1 | 4 | DLG3_chrX_70439835_70510490 | DLG3 | copy fasta | chrX | 70439835 | 70510490 |
| a0001c0001t0004 | 0/0 | 6042 | 7 | 7 | 0 | 0 | 0 | 0 | DLG3_chrX_70439835_70510490 | DLG3 | copy fasta | chrX | 70439835 | 70510490 |
| a0001c0001t0005 | 0/0 | 6043 | 1 | 1 | 0 | 0 | 0 | 0 | DLG3_chrX_70439835_70510490 | DLG3 | copy fasta | chrX | 70439835 | 70510490 |
| a0001c0001t0006 | 0/0 | 6043 | 5 | 0 | 0 | 3 | 0 | 2 | DLG3_chrX_70439835_70510490 | DLG3 | copy fasta | chrX | 70439835 | 70510490 |
| a0001c0001t0007 | 0/0 | 6048 | 4 | 4 | 0 | 0 | 0 | 0 | DLG3_chrX_70439835_70510490 | DLG3 | copy fasta | chrX | 70439835 | 70510490 |
| a0001c0001t0008 | 0/0 | 6041 | 4 | 0 | 0 | 4 | 0 | 0 | DLG3_chrX_70439835_70510490 | DLG3 | copy fasta | chrX | 70439835 | 70510490 |
| a0001c0001t0009 | 0/0 | 6030 | 4 | 0 | 4 | 0 | 0 | 0 | DLG3_chrX_70439835_70510490 | DLG3 | copy fasta | chrX | 70439835 | 70510490 |
| a0001c0001t0010 | 0/0 | 6043 | 3 | 0 | 1 | 0 | 0 | 2 | DLG3_chrX_70439835_70510490 | DLG3 | copy fasta | chrX | 70439835 | 70510490 |
| a0001c0001t0011 | 0/0 | 6042 | 3 | 3 | 0 | 0 | 0 | 0 | DLG3_chrX_70439835_70510490 | DLG3 | copy fasta | chrX | 70439835 | 70510490 |
| a0001c0001t0012 | 0/1 | 6042 | 3 | 0 | 1 | 0 | 1 | 0 | DLG3_chrX_70439835_70510490 | DLG3 | copy fasta | chrX | 70439835 | 70510490 |
| a0001c0001t0013 | 0/0 | 6045 | 1 | 0 | 0 | 1 | 0 | 0 | DLG3_chrX_70439835_70510490 | DLG3 | copy fasta | chrX | 70439835 | 70510490 |
| a0001c0001t0014 | 0/0 | 6043 | 1 | 0 | 0 | 0 | 0 | 1 | DLG3_chrX_70439835_70510490 | DLG3 | copy fasta | chrX | 70439835 | 70510490 |
| a0001c0001t0016 | 0/0 | 6042 | 1 | 0 | 0 | 0 | 0 | 1 | DLG3_chrX_70439835_70510490 | DLG3 | copy fasta | chrX | 70439835 | 70510490 |
| a0001c0001t0017 | 0/0 | 6043 | 1 | 0 | 1 | 0 | 0 | 0 | DLG3_chrX_70439835_70510490 | DLG3 | copy fasta | chrX | 70439835 | 70510490 |
| a0001c0001t0018 | 0/0 | 6042 | 1 | 0 | 0 | 1 | 0 | 0 | DLG3_chrX_70439835_70510490 | DLG3 | copy fasta | chrX | 70439835 | 70510490 |
| a0001c0001t0019 | 0/0 | 6044 | 1 | 1 | 0 | 0 | 0 | 0 | DLG3_chrX_70439835_70510490 | DLG3 | copy fasta | chrX | 70439835 | 70510490 |
| a0001c0001t0020 | 0/0 | 6040 | 1 | 1 | 0 | 0 | 0 | 0 | DLG3_chrX_70439835_70510490 | DLG3 | copy fasta | chrX | 70439835 | 70510490 |
| a0001c0001t0021 | 0/0 | 6042 | 1 | 0 | 0 | 1 | 0 | 0 | DLG3_chrX_70439835_70510490 | DLG3 | copy fasta | chrX | 70439835 | 70510490 |
| a0001c0001t0022 | 0/0 | 6042 | 1 | 1 | 0 | 0 | 0 | 0 | DLG3_chrX_70439835_70510490 | DLG3 | copy fasta | chrX | 70439835 | 70510490 |
| a0001c0001t0023 | 0/0 | 6042 | 1 | 0 | 0 | 0 | 0 | 1 | DLG3_chrX_70439835_70510490 | DLG3 | copy fasta | chrX | 70439835 | 70510490 |
| a0001c0001t0024 | 0/0 | 6042 | 1 | 0 | 1 | 0 | 0 | 0 | DLG3_chrX_70439835_70510490 | DLG3 | copy fasta | chrX | 70439835 | 70510490 |
| a0001c0001t0025 | 0/0 | 6042 | 1 | 1 | 0 | 0 | 0 | 0 | DLG3_chrX_70439835_70510490 | DLG3 | copy fasta | chrX | 70439835 | 70510490 |
| a0001c0001t0026 | 0/0 | 6043 | 1 | 0 | 0 | 0 | 0 | 1 | DLG3_chrX_70439835_70510490 | DLG3 | copy fasta | chrX | 70439835 | 70510490 |
| a0001c0001t0027 | 0/0 | 6043 | 1 | 1 | 0 | 0 | 0 | 0 | DLG3_chrX_70439835_70510490 | DLG3 | copy fasta | chrX | 70439835 | 70510490 |
| a0001c0001t0028 | 0/0 | 6044 | 1 | 1 | 0 | 0 | 0 | 0 | DLG3_chrX_70439835_70510490 | DLG3 | copy fasta | chrX | 70439835 | 70510490 |
| a0001c0001t0029 | 0/0 | 6040 | 1 | 1 | 0 | 0 | 0 | 0 | DLG3_chrX_70439835_70510490 | DLG3 | copy fasta | chrX | 70439835 | 70510490 |
| a0001c0001t0030 | 0/0 | 6043 | 1 | 0 | 0 | 0 | 0 | 1 | DLG3_chrX_70439835_70510490 | DLG3 | copy fasta | chrX | 70439835 | 70510490 |
| a0001c0002t0005 | 0/0 | 6043 | 6 | 4 | 2 | 0 | 0 | 0 | DLG3_chrX_70439835_70510490 | DLG3 | copy fasta | chrX | 70439835 | 70510490 |
| a0001c0007t0002 | 0/0 | 6042 | 1 | 0 | 0 | 1 | 0 | 0 | DLG3_chrX_70439835_70510490 | DLG3 | copy fasta | chrX | 70439835 | 70510490 |
| a0002c0003t0001 | 0/0 | 6041 | 1 | 0 | 0 | 1 | 0 | 0 | DLG3_chrX_70439835_70510490 | DLG3 | copy fasta | chrX | 70439835 | 70510490 |
| a0003c0009t0002 | 0/0 | 6042 | 1 | 0 | 1 | 0 | 0 | 0 | DLG3_chrX_70439835_70510490 | DLG3 | copy fasta | chrX | 70439835 | 70510490 |
| a0004c0005t0001 | 0/0 | 6047 | 1 | 0 | 0 | 1 | 0 | 0 | DLG3_chrX_70439835_70510490 | DLG3 | copy fasta | chrX | 70439835 | 70510490 |
| a0005c0008t0002 | 0/0 | 6043 | 1 | 0 | 0 | 1 | 0 | 0 | DLG3_chrX_70439835_70510490 | DLG3 | copy fasta | chrX | 70439835 | 70510490 |
| a0006c0006t0015 | 0/0 | 6045 | 1 | 0 | 0 | 1 | 0 | 0 | DLG3_chrX_70439835_70510490 | DLG3 | copy fasta | chrX | 70439835 | 70510490 |
| a0007c0004t0002 | 0/0 | 6043 | 1 | 0 | 0 | 1 | 0 | 0 | DLG3_chrX_70439835_70510490 | DLG3 | copy fasta | chrX | 70439835 | 70510490 |
| a0008c0010t0031 | 0/0 | 6061 | 1 | 0 | 0 | 1 | 0 | 0 | DLG3_chrX_70439835_70510490 | DLG3 | copy fasta | chrX | 70439835 | 70510490 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0015 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| a0001c0001t0001g0016 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| a0001c0001t0001g0017 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| a0001c0001t0001g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| a0001c0001t0001g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| a0001c0001t0001g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| a0001c0001t0001g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| a0001c0001t0001g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| a0001c0001t0001g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| a0001c0001t0001g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| a0001c0001t0001g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| a0001c0001t0001g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| a0001c0001t0001g0038 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| a0001c0001t0001g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| a0001c0001t0001g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| a0001c0001t0001g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| a0001c0001t0001g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| a0001c0001t0001g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| a0001c0001t0001g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| a0001c0001t0001g0053 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| a0001c0001t0001g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| a0001c0001t0001g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| a0001c0001t0001g0133 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| a0001c0001t0001g0134 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| a0001c0001t0001g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| a0001c0001t0001g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| a0001c0001t0001g0140 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| a0001c0001t0001g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| a0001c0001t0001g0145 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| a0001c0001t0001g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| a0001c0001t0001g0147 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| a0001c0001t0001g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| a0001c0001t0001g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| a0001c0001t0001g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| a0001c0001t0001g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| a0001c0001t0001g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| a0001c0001t0001g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| a0001c0001t0001g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| a0001c0001t0001g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| a0001c0001t0001g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| a0001c0001t0001g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| a0001c0001t0001g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| a0001c0001t0001g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| a0001c0001t0001g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| a0001c0001t0001g0164 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| a0001c0001t0001g0165 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| a0001c0001t0001g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| a0001c0001t0001g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| a0001c0001t0001g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| a0001c0001t0001g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| a0001c0001t0001g0173 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| a0001c0001t0001g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| a0001c0001t0001g0177 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| a0001c0001t0001g0179 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| a0001c0001t0001g0180 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| a0001c0001t0001g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| a0001c0001t0001g0185 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| a0001c0001t0001g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| a0001c0001t0001g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| a0001c0001t0001g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| a0001c0001t0001g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| a0001c0001t0001g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| a0001c0001t0001g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| a0001c0001t0001g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| a0001c0001t0001g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| a0001c0001t0001g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| a0001c0001t0001g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| a0001c0001t0001g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| a0001c0001t0001g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| a0001c0001t0001g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| a0001c0001t0001g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| a0001c0001t0001g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| a0001c0001t0001g0202 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| a0001c0001t0001g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| a0001c0001t0001g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| a0001c0001t0001g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| a0001c0001t0001g0207 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| a0001c0001t0001g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| a0001c0001t0001g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| a0001c0001t0001g0210 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| a0001c0001t0001g0211 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| a0001c0001t0001g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| a0001c0001t0001g0215 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| a0001c0001t0001g0216 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| a0001c0001t0001g0217 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| a0001c0001t0001g0219 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| a0001c0001t0001g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| a0001c0001t0001g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| a0001c0001t0001g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| a0001c0001t0001g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| a0001c0001t0001g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| a0001c0001t0001g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| a0001c0001t0001g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| a0001c0001t0001g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| a0001c0001t0001g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| a0001c0001t0001g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| a0001c0001t0001g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| a0001c0001t0001g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| a0001c0001t0001g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| a0001c0001t0001g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| a0001c0001t0001g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| a0001c0001t0002g0001 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| a0001c0001t0002g0002 | 0/0 | 5 | 0 | 2 | 2 | 0 | 1 | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| a0001c0001t0002g0003 | 1/0 | 4 | 3 | 0 | 0 | 0 | 0 | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| a0001c0001t0002g0004 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| a0001c0001t0002g0005 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| a0001c0001t0002g0009 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| a0001c0001t0002g0010 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| a0001c0001t0002g0011 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| a0001c0001t0002g0012 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| a0001c0001t0002g0013 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| a0001c0001t0002g0014 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| a0001c0001t0002g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| a0001c0001t0002g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| a0001c0001t0002g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| a0001c0001t0002g0060 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| a0001c0001t0002g0062 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| a0001c0001t0002g0064 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| a0001c0001t0002g0067 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| a0001c0001t0002g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| a0001c0001t0002g0069 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| a0001c0001t0002g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| a0001c0001t0002g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| a0001c0001t0002g0074 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| a0001c0001t0002g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| a0001c0001t0002g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| a0001c0001t0002g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| a0001c0001t0002g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| a0001c0001t0002g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| a0001c0001t0002g0080 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| a0001c0001t0002g0081 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| a0001c0001t0002g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| a0001c0001t0002g0083 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| a0001c0001t0002g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| a0001c0001t0002g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| a0001c0001t0002g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| a0001c0001t0002g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| a0001c0001t0002g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| a0001c0001t0002g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| a0001c0001t0002g0090 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| a0001c0001t0002g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| a0001c0001t0002g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| a0001c0001t0002g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| a0001c0001t0002g0094 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| a0001c0001t0002g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| a0001c0001t0002g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| a0001c0001t0002g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| a0001c0001t0002g0098 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| a0001c0001t0002g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| a0001c0001t0002g0100 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| a0001c0001t0002g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| a0001c0001t0002g0102 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| a0001c0001t0002g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| a0001c0001t0002g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| a0001c0001t0002g0105 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| a0001c0001t0002g0106 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| a0001c0001t0002g0107 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| a0001c0001t0002g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| a0001c0001t0002g0110 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| a0001c0001t0002g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| a0001c0001t0002g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| a0001c0001t0002g0114 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| a0001c0001t0002g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| a0001c0001t0002g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| a0001c0001t0002g0117 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| a0001c0001t0002g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| a0001c0001t0002g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| a0001c0001t0002g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| a0001c0001t0002g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| a0001c0001t0002g0125 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| a0001c0001t0002g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| a0001c0001t0002g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| a0001c0001t0002g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| a0001c0001t0002g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| a0001c0001t0002g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| a0001c0001t0002g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| a0001c0001t0002g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| a0001c0001t0002g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| a0001c0001t0003g0008 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| a0001c0001t0003g0028 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| a0001c0001t0003g0030 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| a0001c0001t0003g0031 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| a0001c0001t0003g0032 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| a0001c0001t0003g0033 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| a0001c0001t0003g0034 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| a0001c0001t0003g0035 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| a0001c0001t0003g0036 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| a0001c0001t0003g0156 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| a0001c0001t0003g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| a0001c0001t0004g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| a0001c0001t0004g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| a0001c0001t0004g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| a0001c0001t0004g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| a0001c0001t0004g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| a0001c0001t0004g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| a0001c0001t0004g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| a0001c0001t0005g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| a0001c0001t0006g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| a0001c0001t0006g0109 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| a0001c0001t0006g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| a0001c0001t0006g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| a0001c0001t0006g0143 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| a0001c0001t0007g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| a0001c0001t0007g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| a0001c0001t0007g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| a0001c0001t0007g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| a0001c0001t0008g0001 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| a0001c0001t0008g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| a0001c0001t0008g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| a0001c0001t0008g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| a0001c0001t0009g0007 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| a0001c0001t0009g0176 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| a0001c0001t0010g0138 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| a0001c0001t0010g0154 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| a0001c0001t0010g0186 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| a0001c0001t0011g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| a0001c0001t0011g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| a0001c0001t0011g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| a0001c0001t0012g0006 | 0/1 | 3 | 0 | 1 | 0 | 1 | 0 | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| a0001c0001t0013g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| a0001c0001t0014g0055 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| a0001c0001t0016g0066 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| a0001c0001t0017g0144 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| a0001c0001t0018g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| a0001c0001t0019g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| a0001c0001t0020g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| a0001c0001t0021g0018 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| a0001c0001t0022g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| a0001c0001t0023g0203 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| a0001c0001t0024g0052 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| a0001c0001t0025g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| a0001c0001t0026g0136 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| a0001c0001t0027g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| a0001c0001t0028g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| a0001c0001t0029g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| a0001c0001t0030g0248 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| a0001c0002t0005g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| a0001c0002t0005g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| a0001c0002t0005g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| a0001c0002t0005g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| a0001c0002t0005g0183 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| a0001c0002t0005g0184 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| a0001c0007t0002g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| a0002c0003t0001g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| a0003c0009t0002g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| a0004c0005t0001g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| a0005c0008t0002g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| a0006c0006t0015g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| a0007c0004t0002g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| a0008c0010t0031g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0003 | g0008 | EUR | GBR | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| HG00099 | hp2 | a0001 | c0001 | t0002 | g0110 | EUR | GBR | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| HG00140 | hp1 | a0001 | c0001 | t0002 | g0014 | EUR | GBR | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| HG00280 | hp1 | a0001 | c0001 | t0002 | g0102 | EUR | FIN | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| HG00438 | hp1 | a0001 | c0007 | t0002 | g0127 | EAS | CHS | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| HG00438 | hp2 | a0001 | c0001 | t0002 | g0077 | EAS | CHS | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| HG00609 | hp1 | a0001 | c0001 | t0002 | g0092 | EAS | CHS | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| HG00621 | hp1 | a0001 | c0001 | t0001 | g0194 | EAS | CHS | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| HG00642 | hp1 | a0001 | c0001 | t0003 | g0030 | AMR | PUR | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| HG00673 | hp1 | a0001 | c0001 | t0002 | g0082 | EAS | CHS | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| HG00733 | hp1 | a0001 | c0001 | t0012 | g0006 | AMR | PUR | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| HG00733 | hp2 | a0001 | c0001 | t0003 | g0036 | AMR | PUR | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| HG00735 | hp1 | a0001 | c0001 | t0001 | g0215 | AMR | PUR | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| HG00735 | hp2 | a0001 | c0001 | t0002 | g0067 | AMR | PUR | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| HG00738 | hp1 | a0001 | c0001 | t0001 | g0185 | AMR | PUR | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| HG00741 | hp1 | a0001 | c0001 | t0001 | g0038 | AMR | PUR | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| HG00741 | hp2 | a0001 | c0001 | t0002 | g0096 | AMR | PUR | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| HG01069 | hp1 | a0001 | c0001 | t0003 | g0035 | AMR | PUR | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| HG01070 | hp1 | a0001 | c0001 | t0003 | g0008 | AMR | PUR | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| HG01070 | hp2 | a0001 | c0001 | t0001 | g0211 | AMR | PUR | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| HG01074 | hp1 | a0003 | c0009 | t0002 | g0065 | AMR | PUR | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| HG01081 | hp1 | a0001 | c0001 | t0002 | g0014 | AMR | PUR | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| HG01081 | hp2 | a0001 | c0001 | t0024 | g0052 | AMR | PUR | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| HG01099 | hp1 | a0001 | c0001 | t0002 | g0101 | AMR | PUR | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| HG01106 | hp1 | a0001 | c0001 | t0001 | g0133 | AMR | PUR | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| HG01109 | hp1 | a0001 | c0001 | t0001 | g0177 | AMR | PUR | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| HG01167 | hp1 | a0001 | c0002 | t0005 | g0184 | AMR | PUR | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| HG01169 | hp1 | a0001 | c0002 | t0005 | g0183 | AMR | PUR | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| HG01169 | hp2 | a0001 | c0001 | t0002 | g0105 | AMR | PUR | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| HG01175 | hp1 | a0001 | c0001 | t0001 | g0140 | AMR | PUR | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| HG01175 | hp2 | a0001 | c0001 | t0002 | g0094 | AMR | PUR | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| HG01192 | hp1 | a0001 | c0001 | t0010 | g0138 | AMR | PUR | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| HG01243 | hp1 | a0001 | c0001 | t0001 | g0216 | AMR | PUR | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| HG01255 | hp1 | a0001 | c0001 | t0001 | g0173 | AMR | CLM | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| HG01256 | hp1 | a0001 | c0001 | t0002 | g0002 | AMR | CLM | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| HG01257 | hp1 | a0001 | c0001 | t0009 | g0176 | AMR | CLM | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| HG01257 | hp2 | a0001 | c0001 | t0002 | g0069 | AMR | CLM | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| HG01258 | hp1 | a0001 | c0001 | t0009 | g0007 | AMR | CLM | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| HG01261 | hp1 | a0001 | c0001 | t0017 | g0144 | AMR | CLM | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| HG01346 | hp1 | a0001 | c0001 | t0001 | g0207 | AMR | CLM | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| HG01346 | hp2 | a0001 | c0001 | t0002 | g0060 | AMR | CLM | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| HG01358 | hp1 | a0001 | c0001 | t0001 | g0217 | AMR | CLM | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| HG01361 | hp1 | a0001 | c0001 | t0001 | g0145 | AMR | CLM | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| HG01361 | hp2 | a0001 | c0001 | t0002 | g0107 | AMR | CLM | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| HG01433 | hp1 | a0001 | c0001 | t0002 | g0098 | AMR | CLM | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| HG01515 | hp1 | a0001 | c0001 | t0002 | g0012 | EUR | IBS | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| HG01516 | hp1 | a0001 | c0001 | t0002 | g0090 | EUR | IBS | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| HG01516 | hp2 | a0001 | c0001 | t0001 | g0180 | EUR | IBS | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| HG01517 | hp1 | a0001 | c0001 | t0001 | g0179 | EUR | IBS | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| HG01517 | hp2 | a0001 | c0001 | t0002 | g0012 | EUR | IBS | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| HG01884 | hp1 | a0001 | c0001 | t0001 | g0226 | AFR | ACB | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| HG01884 | hp2 | a0001 | c0001 | t0002 | g0003 | AFR | ACB | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| HG01891 | hp1 | a0001 | c0001 | t0005 | g0037 | AFR | ACB | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| HG01891 | hp2 | a0001 | c0001 | t0001 | g0240 | AFR | ACB | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| HG01928 | hp1 | a0001 | c0001 | t0001 | g0164 | AMR | PEL | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| HG01934 | hp1 | a0001 | c0001 | t0002 | g0106 | AMR | PEL | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| HG01943 | hp1 | a0001 | c0001 | t0002 | g0002 | AMR | PEL | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| HG01952 | hp1 | a0001 | c0001 | t0009 | g0007 | AMR | PEL | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| HG01993 | hp1 | a0001 | c0001 | t0002 | g0116 | AMR | PEL | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| HG01993 | hp2 | a0001 | c0001 | t0003 | g0033 | AMR | PEL | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| HG02015 | hp1 | a0001 | c0001 | t0001 | g0019 | EAS | KHV | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| HG02027 | hp1 | a0001 | c0001 | t0002 | g0220 | EAS | KHV | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| HG02040 | hp1 | a0001 | c0001 | t0002 | g0009 | EAS | KHV | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| HG02055 | hp1 | a0001 | c0001 | t0004 | g0221 | AFR | ACB | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| HG02056 | hp1 | a0001 | c0001 | t0002 | g0170 | EAS | KHV | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| HG02071 | hp1 | a0001 | c0001 | t0002 | g0112 | EAS | KHV | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| HG02074 | hp1 | a0001 | c0001 | t0002 | g0027 | EAS | KHV | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| HG02083 | hp1 | a0001 | c0001 | t0002 | g0005 | EAS | KHV | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| HG02129 | hp1 | a0001 | c0001 | t0002 | g0093 | EAS | KHV | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| HG02132 | hp1 | a0001 | c0001 | t0002 | g0128 | EAS | KHV | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| HG02135 | hp1 | a0001 | c0001 | t0002 | g0013 | EAS | KHV | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| HG02145 | hp1 | a0001 | c0001 | t0028 | g0223 | AFR | ACB | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| HG02155 | hp1 | a0001 | c0001 | t0001 | g0162 | EAS | CDX | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| HG02155 | hp2 | a0001 | c0001 | t0001 | g0059 | EAS | CDX | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| HG02165 | hp1 | a0001 | c0001 | t0001 | g0192 | EAS | CDX | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| HG02165 | hp2 | a0001 | c0001 | t0002 | g0087 | EAS | CDX | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| HG02257 | hp1 | a0001 | c0001 | t0001 | g0017 | AFR | ACB | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| HG02257 | hp2 | a0001 | c0001 | t0004 | g0232 | AFR | ACB | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| HG02258 | hp1 | a0001 | c0001 | t0001 | g0021 | AFR | ACB | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| HG02280 | hp1 | a0001 | c0001 | t0001 | g0029 | AFR | ACB | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| HG02280 | hp2 | a0001 | c0001 | t0007 | g0178 | AFR | ACB | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| HG02451 | hp1 | a0001 | c0001 | t0001 | g0231 | AFR | ACB | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| HG02451 | hp2 | a0001 | c0001 | t0001 | g0239 | AFR | ACB | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| HG02523 | hp1 | a0001 | c0001 | t0001 | g0195 | EAS | KHV | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| HG02523 | hp2 | a0001 | c0001 | t0002 | g0115 | EAS | KHV | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| HG02572 | hp1 | a0001 | c0001 | t0001 | g0045 | AFR | GWD | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| HG02602 | hp1 | a0001 | c0001 | t0002 | g0125 | SAS | PJL | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| HG02615 | hp1 | a0001 | c0001 | t0001 | g0205 | AFR | GWD | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| HG02615 | hp2 | a0001 | c0001 | t0001 | g0046 | AFR | GWD | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| HG02622 | hp1 | a0001 | c0001 | t0001 | g0243 | AFR | GWD | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| HG02622 | hp2 | a0001 | c0001 | t0001 | g0049 | AFR | GWD | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| HG02630 | hp1 | a0001 | c0001 | t0001 | g0187 | AFR | GWD | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| HG02630 | hp2 | a0001 | c0001 | t0001 | g0204 | AFR | GWD | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| HG02647 | hp1 | a0001 | c0001 | t0001 | g0142 | AFR | GWD | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| HG02683 | hp1 | a0001 | c0001 | t0002 | g0064 | SAS | PJL | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| HG02683 | hp2 | a0001 | c0001 | t0002 | g0081 | SAS | PJL | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| HG02698 | hp1 | a0001 | c0001 | t0002 | g0002 | SAS | PJL | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| HG02717 | hp1 | a0001 | c0001 | t0025 | g0139 | AFR | GWD | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| HG02735 | hp1 | a0001 | c0001 | t0001 | g0053 | SAS | PJL | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| HG02738 | hp1 | a0001 | c0001 | t0010 | g0154 | SAS | PJL | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| HG02809 | hp1 | a0001 | c0001 | t0001 | g0209 | AFR | GWD | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| HG02809 | hp2 | a0001 | c0001 | t0002 | g0085 | AFR | GWD | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| HG02886 | hp1 | a0001 | c0001 | t0020 | g0218 | AFR | GWD | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| HG02886 | hp2 | a0001 | c0001 | t0022 | g0227 | AFR | GWD | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| HG02895 | hp1 | a0001 | c0002 | t0005 | g0041 | AFR | GWD | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| HG02896 | hp1 | a0001 | c0001 | t0002 | g0068 | AFR | GWD | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| HG02896 | hp2 | a0001 | c0001 | t0001 | g0229 | AFR | GWD | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| HG02897 | hp1 | a0001 | c0001 | t0001 | g0228 | AFR | GWD | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| HG02897 | hp2 | a0001 | c0002 | t0005 | g0040 | AFR | GWD | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| HG02922 | hp1 | a0001 | c0001 | t0004 | g0233 | AFR | ESN | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| HG02922 | hp2 | a0001 | c0001 | t0001 | g0020 | AFR | ESN | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| HG02965 | hp1 | a0001 | c0001 | t0001 | g0017 | AFR | ESN | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| HG02970 | hp1 | a0001 | c0001 | t0001 | g0241 | AFR | ESN | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| HG02970 | hp2 | a0001 | c0001 | t0029 | g0238 | AFR | ESN | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| HG02976 | hp1 | a0001 | c0001 | t0001 | g0174 | AFR | ESN | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| HG02976 | hp2 | a0001 | c0001 | t0002 | g0003 | AFR | ESN | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| HG03017 | hp1 | a0001 | c0001 | t0003 | g0034 | SAS | PJL | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| HG03041 | hp1 | a0001 | c0001 | t0001 | g0225 | AFR | GWD | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| HG03041 | hp2 | a0001 | c0001 | t0001 | g0044 | AFR | GWD | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| HG03098 | hp1 | a0001 | c0001 | t0004 | g0181 | AFR | MSL | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| HG03130 | hp1 | a0001 | c0001 | t0001 | g0047 | AFR | ESN | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| HG03139 | hp1 | a0001 | c0001 | t0001 | g0213 | AFR | ESN | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| HG03209 | hp1 | a0001 | c0001 | t0001 | g0230 | AFR | MSL | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| HG03225 | hp1 | a0001 | c0001 | t0001 | g0224 | AFR | MSL | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| HG03239 | hp1 | a0001 | c0001 | t0002 | g0114 | SAS | PJL | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| HG03239 | hp2 | a0001 | c0001 | t0003 | g0156 | SAS | PJL | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| HG03453 | hp1 | a0001 | c0001 | t0001 | g0206 | AFR | MSL | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| HG03453 | hp2 | a0001 | c0001 | t0001 | g0235 | AFR | MSL | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| HG03486 | hp1 | a0001 | c0002 | t0005 | g0042 | AFR | MSL | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| HG03486 | hp2 | a0001 | c0001 | t0007 | g0175 | AFR | MSL | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| HG03490 | hp1 | a0001 | c0001 | t0001 | g0202 | SAS | PJL | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| HG03491 | hp1 | a0001 | c0001 | t0001 | g0134 | SAS | PJL | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| HG03491 | hp2 | a0001 | c0001 | t0002 | g0083 | SAS | PJL | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| HG03492 | hp1 | a0001 | c0001 | t0001 | g0219 | SAS | PJL | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| HG03540 | hp1 | a0001 | c0001 | t0004 | g0222 | AFR | GWD | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| HG03540 | hp2 | a0001 | c0001 | t0011 | g0214 | AFR | GWD | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| HG03579 | hp1 | a0001 | c0001 | t0001 | g0208 | AFR | MSL | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| HG03654 | hp1 | a0001 | c0001 | t0002 | g0117 | SAS | PJL | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| HG03669 | hp1 | a0001 | c0001 | t0003 | g0028 | SAS | PJL | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| HG03669 | hp2 | a0001 | c0001 | t0006 | g0109 | SAS | PJL | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| HG03688 | hp1 | a0001 | c0001 | t0016 | g0066 | SAS | STU | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| HG03704 | hp1 | a0001 | c0001 | t0003 | g0031 | SAS | PJL | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| HG03704 | hp2 | a0001 | c0001 | t0002 | g0100 | SAS | PJL | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| HG03710 | hp1 | a0001 | c0001 | t0001 | g0165 | SAS | PJL | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| HG03831 | hp1 | a0001 | c0001 | t0014 | g0055 | SAS | BEB | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| HG03831 | hp2 | a0001 | c0001 | t0010 | g0186 | SAS | BEB | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| HG03927 | hp1 | a0001 | c0001 | t0026 | g0136 | SAS | BEB | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| HG03927 | hp2 | a0001 | c0001 | t0030 | g0248 | SAS | BEB | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| HG03942 | hp1 | a0001 | c0001 | t0023 | g0203 | SAS | BEB | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| HG04115 | hp1 | a0001 | c0001 | t0006 | g0143 | SAS | STU | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| HG04199 | hp1 | a0001 | c0001 | t0002 | g0080 | SAS | STU | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| HG04204 | hp1 | a0001 | c0001 | t0001 | g0147 | SAS | STU | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| HG04228 | hp1 | a0001 | c0001 | t0002 | g0074 | SAS | STU | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| NA18522 | hp1 | a0001 | c0001 | t0001 | g0137 | AFR | YRI | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| NA18612 | hp1 | a0001 | c0001 | t0002 | g0075 | EAS | CHB | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| NA18747 | hp1 | a0001 | c0001 | t0001 | g0163 | EAS | CHB | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| NA18906 | hp1 | a0001 | c0001 | t0004 | g0234 | AFR | YRI | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| NA18906 | hp2 | a0001 | c0001 | t0027 | g0051 | AFR | YRI | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| NA18940 | hp1 | a0001 | c0001 | t0001 | g0200 | EAS | JPT | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| NA18941 | hp1 | a0001 | c0001 | t0002 | g0009 | EAS | JPT | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| NA18941 | hp2 | a0001 | c0001 | t0001 | g0152 | EAS | JPT | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| NA18942 | hp1 | a0001 | c0001 | t0008 | g0063 | EAS | JPT | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| NA18942 | hp2 | a0001 | c0001 | t0001 | g0166 | EAS | JPT | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| NA18943 | hp1 | a0001 | c0001 | t0002 | g0004 | EAS | JPT | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| NA18944 | hp1 | a0001 | c0001 | t0001 | g0016 | EAS | JPT | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| NA18945 | hp1 | a0001 | c0001 | t0001 | g0015 | EAS | JPT | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| NA18946 | hp1 | a0001 | c0001 | t0001 | g0198 | EAS | JPT | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| NA18946 | hp2 | a0001 | c0001 | t0001 | g0160 | EAS | JPT | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| NA18947 | hp1 | a0001 | c0001 | t0002 | g0113 | EAS | JPT | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| NA18947 | hp2 | a0001 | c0001 | t0001 | g0058 | EAS | JPT | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| NA18948 | hp1 | a0001 | c0001 | t0002 | g0103 | EAS | JPT | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| NA18949 | hp1 | a0006 | c0006 | t0015 | g0057 | EAS | JPT | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| NA18949 | hp2 | a0001 | c0001 | t0001 | g0196 | EAS | JPT | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| NA18950 | hp1 | a0001 | c0001 | t0002 | g0004 | EAS | JPT | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| NA18950 | hp2 | a0001 | c0001 | t0001 | g0024 | EAS | JPT | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| NA18951 | hp1 | a0001 | c0001 | t0002 | g0104 | EAS | JPT | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| NA18951 | hp2 | a0001 | c0001 | t0001 | g0157 | EAS | JPT | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| NA18952 | hp1 | a0001 | c0001 | t0002 | g0004 | EAS | JPT | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| NA18953 | hp1 | a0001 | c0001 | t0001 | g0161 | EAS | JPT | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| NA18956 | hp1 | a0001 | c0001 | t0002 | g0011 | EAS | JPT | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| NA18956 | hp2 | a0001 | c0001 | t0002 | g0153 | EAS | JPT | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| NA18957 | hp1 | a0001 | c0001 | t0001 | g0193 | EAS | JPT | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| NA18957 | hp2 | a0001 | c0001 | t0002 | g0056 | EAS | JPT | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| NA18959 | hp1 | a0004 | c0005 | t0001 | g0172 | EAS | JPT | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| NA18960 | hp1 | a0001 | c0001 | t0002 | g0097 | EAS | JPT | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| NA18961 | hp1 | a0001 | c0001 | t0002 | g0089 | EAS | JPT | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| NA18962 | hp1 | a0001 | c0001 | t0002 | g0072 | EAS | JPT | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| NA18964 | hp1 | a0001 | c0001 | t0002 | g0095 | EAS | JPT | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| NA18964 | hp2 | a0001 | c0001 | t0001 | g0167 | EAS | JPT | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| NA18966 | hp1 | a0001 | c0001 | t0006 | g0111 | EAS | JPT | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| NA18967 | hp1 | a0001 | c0001 | t0001 | g0189 | EAS | JPT | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| NA18968 | hp1 | a0001 | c0001 | t0001 | g0249 | EAS | JPT | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| NA18968 | hp2 | a0001 | c0001 | t0002 | g0013 | EAS | JPT | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| NA18970 | hp1 | a0001 | c0001 | t0002 | g0010 | EAS | JPT | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| NA18971 | hp1 | a0001 | c0001 | t0002 | g0121 | EAS | JPT | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| NA18972 | hp1 | a0001 | c0001 | t0001 | g0188 | EAS | JPT | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| NA18972 | hp2 | a0007 | c0004 | t0002 | g0131 | EAS | JPT | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| NA18974 | hp1 | a0001 | c0001 | t0001 | g0169 | EAS | JPT | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| NA18977 | hp1 | a0001 | c0001 | t0002 | g0122 | EAS | JPT | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| NA18980 | hp1 | a0001 | c0001 | t0001 | g0148 | EAS | JPT | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| NA18980 | hp2 | a0001 | c0001 | t0002 | g0091 | EAS | JPT | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| NA18982 | hp1 | a0001 | c0001 | t0002 | g0126 | EAS | JPT | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| NA18983 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| NA18984 | hp1 | a0001 | c0001 | t0002 | g0054 | EAS | JPT | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| NA18988 | hp1 | a0005 | c0008 | t0002 | g0129 | EAS | JPT | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| NA18989 | hp1 | a0008 | c0010 | t0031 | g0245 | EAS | JPT | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| NA18990 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| NA18991 | hp1 | a0001 | c0001 | t0006 | g0124 | EAS | JPT | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| NA18991 | hp2 | a0001 | c0001 | t0001 | g0201 | EAS | JPT | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| NA18993 | hp1 | a0001 | c0001 | t0002 | g0005 | EAS | JPT | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| NA18993 | hp2 | a0001 | c0001 | t0001 | g0171 | EAS | JPT | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| NA18994 | hp1 | a0001 | c0001 | t0008 | g0073 | EAS | JPT | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| NA18995 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| NA18999 | hp1 | a0001 | c0001 | t0002 | g0108 | EAS | JPT | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| NA18999 | hp2 | a0001 | c0001 | t0001 | g0191 | EAS | JPT | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| NA19000 | hp1 | a0001 | c0001 | t0001 | g0158 | EAS | JPT | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| NA19002 | hp1 | a0001 | c0001 | t0008 | g0123 | EAS | JPT | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| NA19002 | hp2 | a0001 | c0001 | t0001 | g0149 | EAS | JPT | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| NA19003 | hp1 | a0001 | c0001 | t0008 | g0001 | EAS | JPT | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| NA19003 | hp2 | a0001 | c0001 | t0001 | g0197 | EAS | JPT | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| NA19004 | hp1 | a0001 | c0001 | t0001 | g0016 | EAS | JPT | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| NA19005 | hp1 | a0001 | c0001 | t0001 | g0023 | EAS | JPT | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| NA19007 | hp1 | a0001 | c0001 | t0002 | g0076 | EAS | JPT | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| NA19009 | hp1 | a0001 | c0001 | t0002 | g0088 | EAS | JPT | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| NA19010 | hp1 | a0001 | c0001 | t0001 | g0015 | EAS | JPT | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| NA19010 | hp2 | a0001 | c0001 | t0002 | g0120 | EAS | JPT | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| NA19011 | hp1 | a0001 | c0001 | t0001 | g0151 | EAS | JPT | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| NA19011 | hp2 | a0001 | c0001 | t0006 | g0061 | EAS | JPT | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| NA19012 | hp1 | a0001 | c0001 | t0001 | g0155 | EAS | JPT | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| NA19030 | hp1 | a0001 | c0001 | t0019 | g0141 | AFR | LWK | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| NA19030 | hp2 | a0001 | c0001 | t0001 | g0026 | AFR | LWK | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| NA19043 | hp1 | a0001 | c0001 | t0004 | g0119 | AFR | LWK | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| NA19055 | hp1 | a0001 | c0001 | t0002 | g0130 | EAS | JPT | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| NA19056 | hp1 | a0001 | c0001 | t0002 | g0132 | EAS | JPT | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| NA19058 | hp1 | a0002 | c0003 | t0001 | g0246 | EAS | JPT | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| NA19060 | hp1 | a0001 | c0001 | t0001 | g0190 | EAS | JPT | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| NA19063 | hp1 | a0001 | c0001 | t0018 | g0070 | EAS | JPT | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| NA19064 | hp1 | a0001 | c0001 | t0001 | g0159 | EAS | JPT | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| NA19064 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| NA19065 | hp1 | a0001 | c0001 | t0001 | g0199 | EAS | JPT | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| NA19065 | hp2 | a0001 | c0001 | t0002 | g0084 | EAS | JPT | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| NA19066 | hp1 | a0001 | c0001 | t0002 | g0078 | EAS | JPT | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| NA19067 | hp1 | a0001 | c0001 | t0001 | g0146 | EAS | JPT | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| NA19068 | hp1 | a0001 | c0001 | t0002 | g0079 | EAS | JPT | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| NA19070 | hp1 | a0001 | c0001 | t0002 | g0011 | EAS | JPT | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| NA19074 | hp1 | a0001 | c0001 | t0001 | g0150 | EAS | JPT | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| NA19074 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| NA19076 | hp1 | a0001 | c0001 | t0013 | g0244 | EAS | JPT | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| NA19077 | hp1 | a0001 | c0001 | t0002 | g0086 | EAS | JPT | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| NA19077 | hp2 | a0001 | c0001 | t0002 | g0071 | EAS | JPT | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| NA19079 | hp1 | a0001 | c0001 | t0002 | g0010 | EAS | JPT | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| NA19082 | hp1 | a0001 | c0001 | t0002 | g0118 | EAS | JPT | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| NA19083 | hp1 | a0001 | c0001 | t0002 | g0247 | EAS | JPT | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| NA19085 | hp1 | a0001 | c0001 | t0021 | g0018 | EAS | JPT | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| NA19087 | hp1 | a0001 | c0001 | t0001 | g0025 | EAS | JPT | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| NA19087 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| NA19088 | hp1 | a0001 | c0001 | t0002 | g0099 | EAS | JPT | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| NA19091 | hp1 | a0001 | c0001 | t0002 | g0005 | EAS | JPT | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| NA19240 | hp1 | a0001 | c0001 | t0002 | g0003 | AFR | YRI | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| NA19240 | hp2 | a0001 | c0001 | t0001 | g0182 | AFR | YRI | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| NA20752 | hp1 | a0001 | c0001 | t0012 | g0006 | EUR | TSI | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| NA20805 | hp1 | a0001 | c0001 | t0001 | g0210 | EUR | TSI | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| NA20905 | hp1 | a0001 | c0001 | t0002 | g0062 | SAS | GIH | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| HG01123 | hp1 | a0001 | c0001 | t0009 | g0007 | AMR | CLM | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| HG01123 | hp2 | a0001 | c0001 | t0003 | g0032 | AMR | CLM | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| HG02109 | hp1 | a0001 | c0001 | t0001 | g0022 | AFR | ACB | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| HG02109 | hp2 | a0001 | c0001 | t0001 | g0237 | AFR | ACB | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| HG02486 | hp1 | a0001 | c0002 | t0005 | g0039 | AFR | ACB | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| HG02559 | hp1 | a0001 | c0001 | t0007 | g0050 | AFR | ACB | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| HG02559 | hp2 | a0001 | c0001 | t0007 | g0212 | AFR | ACB | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| HG03471 | hp1 | a0001 | c0001 | t0001 | g0236 | AFR | MSL | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| HG06807 | hp1 | a0001 | c0001 | t0001 | g0048 | AFR | USA | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| HG06807 | hp2 | a0001 | c0001 | t0011 | g0242 | AFR | USA | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| NA18955 | hp1 | a0001 | c0001 | t0001 | g0135 | EAS | JPT | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| NA20300 | hp1 | a0001 | c0001 | t0011 | g0043 | AFR | USA | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| NA20300 | hp2 | a0001 | c0001 | t0003 | g0168 | AFR | USA | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0012 | g0006 | REF | REF | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| homoSapiens_grch38 | hp1 | a0001 | c0001 | t0002 | g0003 | REF | REF | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| 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:70445327
|
T | TG | 1 | a0008 | 1 | NA18989.hp1 | frameshift_variant | HIGH | c.131dupG | p.Asn45fs | DLG3 | ENSG00000082458.12 | transcript | ENST00000374360.8 | protein_coding | 1/19 | 499/6042 | 132/2454 | 44/817 | INFO_REALIGN_3_PRIME | chrX | 70445327 | |
| chrX:70445327
|
TG | T | 1 | a0002 | 1 | NA19058.hp1 | frameshift_variant | HIGH | c.131delG | p.Gly44fs | DLG3 | ENSG00000082458.12 | transcript | ENST00000374360.8 | protein_coding | 1/19 | 498/6042 | 131/2454 | 44/817 | INFO_REALIGN_3_PRIME | chrX | 70445327 | |
| chrX:70445351
|
T | TG | 1 | a0008 | 1 | NA18989.hp1 | frameshift_variant | HIGH | c.150_151insG | p.Tyr51fs | DLG3 | ENSG00000082458.12 | transcript | ENST00000374360.8 | protein_coding | 1/19 | 518/6042 | 151/2454 | 51/817 | chrX | 70445351 | ||
| chrX:70445354
|
TG | T | 1 | a0002 | 1 | NA19058.hp1 | frameshift_variant | HIGH | c.158delG | p.Gly53fs | DLG3 | ENSG00000082458.12 | transcript | ENST00000374360.8 | protein_coding | 1/19 | 525/6042 | 158/2454 | 53/817 | INFO_REALIGN_3_PRIME | chrX | 70445354 | |
| chrX:70445397
|
A | AC | 1 | a0008 | 1 | NA18989.hp1 | frameshift_variant | HIGH | c.201dupC | p.Thr68fs | DLG3 | ENSG00000082458.12 | transcript | ENST00000374360.8 | protein_coding | 1/19 | 569/6042 | 202/2454 | 68/817 | INFO_REALIGN_3_PRIME | chrX | 70445397 | |
| chrX:70445403
|
A | AC | 1 | a0007 | 1 | NA18972.hp2 | frameshift_variant | HIGH | c.206dupC | p.Arg70fs | DLG3 | ENSG00000082458.12 | transcript | ENST00000374360.8 | protein_coding | 1/19 | 574/6042 | 207/2454 | 69/817 | INFO_REALIGN_3_PRIME | chrX | 70445403 | |
| chrX:70445418
|
G | GA | 1 | a0008 | 1 | NA18989.hp1 | frameshift_variant | HIGH | c.217_218insA | p.Ala73fs | DLG3 | ENSG00000082458.12 | transcript | ENST00000374360.8 | protein_coding | 1/19 | 585/6042 | 218/2454 | 73/817 | chrX | 70445418 | ||
| chrX:70445432
|
C | CG | 1 | a0008 | 1 | NA18989.hp1 | frameshift_variant | HIGH | c.231_232insG | p.Thr78fs | DLG3 | ENSG00000082458.12 | transcript | ENST00000374360.8 | protein_coding | 1/19 | 599/6042 | 232/2454 | 78/817 | chrX | 70445432 | ||
| chrX:70445484
|
A | AC | 1 | a0008 | 1 | NA18989.hp1 | frameshift_variant | HIGH | c.288dupC | p.Lys97fs | DLG3 | ENSG00000082458.12 | transcript | ENST00000374360.8 | protein_coding | 1/19 | 656/6042 | 289/2454 | 97/817 | INFO_REALIGN_3_PRIME | chrX | 70445484 | |
| chrX:70445489
|
C | CA | 1 | a0002 | 1 | NA19058.hp1 | frameshift_variant | HIGH | c.291dupA | p.Leu98fs | DLG3 | ENSG00000082458.12 | transcript | ENST00000374360.8 | protein_coding | 1/19 | 659/6042 | 292/2454 | 98/817 | INFO_REALIGN_3_PRIME | chrX | 70445489 | |
| chrX:70445506
|
G | GC | 1 | a0008 | 1 | NA18989.hp1 | frameshift_variant | HIGH | c.309dupC | p.Ser104fs | DLG3 | ENSG00000082458.12 | transcript | ENST00000374360.8 | protein_coding | 1/19 | 677/6042 | 310/2454 | 104/817 | INFO_REALIGN_3_PRIME | chrX | 70445506 | |
| chrX:70445514
|
T | TG | 1 | a0008 | 1 | NA18989.hp1 | frameshift_variant | HIGH | c.315dupG | p.Trp106fs | DLG3 | ENSG00000082458.12 | transcript | ENST00000374360.8 | protein_coding | 1/19 | 683/6042 | 316/2454 | 106/817 | INFO_REALIGN_3_PRIME | chrX | 70445514 | |
| chrX:70445541
|
C | CG | 1 | a0008 | 1 | NA18989.hp1 | frameshift_variant | HIGH | c.343dupG | p.Asp115fs | DLG3 | ENSG00000082458.12 | transcript | ENST00000374360.8 | protein_coding | 1/19 | 711/6042 | 344/2454 | 115/817 | INFO_REALIGN_3_PRIME | chrX | 70445541 | |
| chrX:70449752
|
C | CG | 1 | a0008 | 1 | NA18989.hp1 | frameshift_variant | HIGH | c.598dupG | p.Val200fs | DLG3 | ENSG00000082458.12 | transcript | ENST00000374360.8 | protein_coding | 4/19 | 966/6042 | 599/2454 | 200/817 | INFO_REALIGN_3_PRIME | chrX | 70449752 | |
| chrX:70450172
|
T | TG | 1 | a0008 | 1 | NA18989.hp1 | frameshift_variant | HIGH | c.710dupG | p.Ser239fs | DLG3 | ENSG00000082458.12 | transcript | ENST00000374360.8 | protein_coding | 5/19 | 1078/6042 | 711/2454 | 237/817 | INFO_REALIGN_3_PRIME | chrX | 70450172 | |
| chrX:70450250
|
A | AG | 1 | a0002 | 1 | NA19058.hp1 | frameshift_variant | HIGH | c.791dupG | p.Ala265fs | DLG3 | ENSG00000082458.12 | transcript | ENST00000374360.8 | protein_coding | 5/19 | 1159/6042 | 792/2454 | 264/817 | INFO_REALIGN_3_PRIME | chrX | 70450250 | |
| chrX:70450276
|
C | T | 1 | a0003 | 1 | HG01074.hp1 | missense_variant | MODERATE | c.811C>T | p.Arg271Cys | DLG3 | ENSG00000082458.12 | transcript | ENST00000374360.8 | protein_coding | 5/19 | 1178/6042 | 811/2454 | 271/817 | chrX | 70450276 | ||
| chrX:70451867
|
C | A | 1 | a0004 | 1 | NA18959.hp1 | missense_variant&splice_region_variant | MODERATE | c.986C>A | p.Thr329Asn | DLG3 | ENSG00000082458.12 | transcript | ENST00000374360.8 | protein_coding | 7/19 | 1353/6042 | 986/2454 | 329/817 | chrX | 70451867 | ||
| chrX:70451869
|
T | G | 1 | a0004 | 1 | NA18959.hp1 | missense_variant&splice_region_variant | MODERATE | c.988T>G | p.Phe330Val | DLG3 | ENSG00000082458.12 | transcript | ENST00000374360.8 | protein_coding | 7/19 | 1355/6042 | 988/2454 | 330/817 | chrX | 70451869 | ||
| chrX:70451870
|
T | G | 1 | a0004 | 1 | NA18959.hp1 | missense_variant | MODERATE | c.989T>G | p.Phe330Cys | DLG3 | ENSG00000082458.12 | transcript | ENST00000374360.8 | protein_coding | 7/19 | 1356/6042 | 989/2454 | 330/817 | chrX | 70451870 | ||
| chrX:70451874
|
TGC | T | 1 | a0004 | 1 | NA18959.hp1 | frameshift_variant | HIGH | c.994_995delGC | p.Ala332fs | DLG3 | ENSG00000082458.12 | transcript | ENST00000374360.8 | protein_coding | 7/19 | 1361/6042 | 994/2454 | 332/817 | chrX | 70451874 | ||
| chrX:70451878
|
T | G | 1 | a0004 | 1 | NA18959.hp1 | missense_variant | MODERATE | c.997T>G | p.Leu333Val | DLG3 | ENSG00000082458.12 | transcript | ENST00000374360.8 | protein_coding | 7/19 | 1364/6042 | 997/2454 | 333/817 | chrX | 70451878 | ||
| chrX:70451882
|
C | CAGT | 1 | a0004 | 1 | NA18959.hp1 | disruptive_inframe_insertion | MODERATE | c.1001_1002insAGT | p.Ala334_Asp335insVa others(1): Show |
DLG3 | ENSG00000082458.12 | transcript | ENST00000374360.8 | protein_coding | 7/19 | 1369/6042 | 1002/2454 | 334/817 | chrX | 70451882 | ||
| chrX:70451884
|
G | C | 1 | a0004 | 1 | NA18959.hp1 | missense_variant | MODERATE | c.1003G>C | p.Asp335His | DLG3 | ENSG00000082458.12 | transcript | ENST00000374360.8 | protein_coding | 7/19 | 1370/6042 | 1003/2454 | 335/817 | chrX | 70451884 | ||
| chrX:70451885
|
A | T | 1 | a0004 | 1 | NA18959.hp1 | missense_variant | MODERATE | c.1004A>T | p.Asp335Val | DLG3 | ENSG00000082458.12 | transcript | ENST00000374360.8 | protein_coding | 7/19 | 1371/6042 | 1004/2454 | 335/817 | chrX | 70451885 | ||
| chrX:70451888
|
A | G | 1 | a0004 | 1 | NA18959.hp1 | missense_variant | MODERATE | c.1007A>G | p.Asn336Ser | DLG3 | ENSG00000082458.12 | transcript | ENST00000374360.8 | protein_coding | 7/19 | 1374/6042 | 1007/2454 | 336/817 | chrX | 70451888 | ||
| chrX:70451889
|
C | A | 1 | a0004 | 1 | NA18959.hp1 | missense_variant | MODERATE | c.1008C>A | p.Asn336Lys | DLG3 | ENSG00000082458.12 | transcript | ENST00000374360.8 | protein_coding | 7/19 | 1375/6042 | 1008/2454 | 336/817 | chrX | 70451889 | ||
| chrX:70451891
|
A | T | 1 | a0004 | 1 | NA18959.hp1 | missense_variant | MODERATE | c.1010A>T | p.His337Leu | DLG3 | ENSG00000082458.12 | transcript | ENST00000374360.8 | protein_coding | 7/19 | 1377/6042 | 1010/2454 | 337/817 | chrX | 70451891 | ||
| chrX:70451892
|
C | A | 1 | a0004 | 1 | NA18959.hp1 | missense_variant | MODERATE | c.1011C>A | p.His337Gln | DLG3 | ENSG00000082458.12 | transcript | ENST00000374360.8 | protein_coding | 7/19 | 1378/6042 | 1011/2454 | 337/817 | chrX | 70451892 | ||
| chrX:70451893
|
A | T | 1 | a0004 | 1 | NA18959.hp1 | missense_variant | MODERATE | c.1012A>T | p.Ile338Leu | DLG3 | ENSG00000082458.12 | transcript | ENST00000374360.8 | protein_coding | 7/19 | 1379/6042 | 1012/2454 | 338/817 | chrX | 70451893 | ||
| chrX:70451896
|
A | T | 1 | a0004 | 1 | NA18959.hp1 | missense_variant | MODERATE | c.1015A>T | p.Ser339Cys | DLG3 | ENSG00000082458.12 | transcript | ENST00000374360.8 | protein_coding | 7/19 | 1382/6042 | 1015/2454 | 339/817 | chrX | 70451896 | ||
| chrX:70451898
|
C | A | 1 | a0004 | 1 | NA18959.hp1 | missense_variant | MODERATE | c.1017C>A | p.Ser339Arg | DLG3 | ENSG00000082458.12 | transcript | ENST00000374360.8 | protein_coding | 7/19 | 1384/6042 | 1017/2454 | 339/817 | chrX | 70451898 | ||
| chrX:70451901
|
T | TTTCG | 1 | a0004 | 1 | NA18959.hp1 | frameshift_variant | HIGH | c.1020_1021insTTCG | p.Asn341fs | DLG3 | ENSG00000082458.12 | transcript | ENST00000374360.8 | protein_coding | 7/19 | 1388/6042 | 1021/2454 | 341/817 | chrX | 70451901 | ||
| chrX:70451902
|
A | T | 1 | a0004 | 1 | NA18959.hp1 | missense_variant | MODERATE | c.1021A>T | p.Asn341Tyr | DLG3 | ENSG00000082458.12 | transcript | ENST00000374360.8 | protein_coding | 7/19 | 1388/6042 | 1021/2454 | 341/817 | chrX | 70451902 | ||
| chrX:70451903
|
A | G | 1 | a0004 | 1 | NA18959.hp1 | missense_variant | MODERATE | c.1022A>G | p.Asn341Ser | DLG3 | ENSG00000082458.12 | transcript | ENST00000374360.8 | protein_coding | 7/19 | 1389/6042 | 1022/2454 | 341/817 | chrX | 70451903 | ||
| chrX:70451906
|
C | T | 1 | a0004 | 1 | NA18959.hp1 | missense_variant | MODERATE | c.1025C>T | p.Ser342Phe | DLG3 | ENSG00000082458.12 | transcript | ENST00000374360.8 | protein_coding | 7/19 | 1392/6042 | 1025/2454 | 342/817 | chrX | 70451906 | ||
| chrX:70451967
|
TC | T | 1 | a0002 | 1 | NA19058.hp1 | frameshift_variant | HIGH | c.1092delC | p.Thr365fs | DLG3 | ENSG00000082458.12 | transcript | ENST00000374360.8 | protein_coding | 7/19 | 1459/6042 | 1092/2454 | 364/817 | INFO_REALIGN_3_PRIME | chrX | 70451967 | |
| chrX:70453710
|
G | GA | 1 | a0006 | 1 | NA18949.hp1 | frameshift_variant | HIGH | c.1221dupA | p.Gly408fs | DLG3 | ENSG00000082458.12 | transcript | ENST00000374360.8 | protein_coding | 8/19 | 1589/6042 | 1222/2454 | 408/817 | INFO_REALIGN_3_PRIME | chrX | 70453710 | |
| chrX:70453716
|
A | AT | 1 | a0005 | 1 | NA18988.hp1 | frameshift_variant | HIGH | c.1230dupT | p.Val411fs | DLG3 | ENSG00000082458.12 | transcript | ENST00000374360.8 | protein_coding | 8/19 | 1598/6042 | 1231/2454 | 411/817 | INFO_REALIGN_3_PRIME | chrX | 70453716 | |
| chrX:70454254
|
C | CT | 1 | a0006 | 1 | NA18949.hp1 | frameshift_variant | HIGH | c.1344dupT | p.Ala449fs | DLG3 | ENSG00000082458.12 | transcript | ENST00000374360.8 | protein_coding | 9/19 | 1712/6042 | 1345/2454 | 449/817 | INFO_REALIGN_3_PRIME | chrX | 70454254 |
| 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:70451877
|
C | A | 1 | a0004c0005 | 1 | NA18959.hp1 | synonymous_variant | LOW | c.996C>A | p.Ala332Ala | DLG3 | ENSG00000082458.12 | transcript | ENST00000374360.8 | protein_coding | 7/19 | 1363/6042 | 996/2454 | 332/817 | chrX | 70451877 | ||
| chrX:70451886
|
C | T | 1 | a0004c0005 | 1 | NA18959.hp1 | synonymous_variant | LOW | c.1005C>T | p.Asp335Asp | DLG3 | ENSG00000082458.12 | transcript | ENST00000374360.8 | protein_coding | 7/19 | 1372/6042 | 1005/2454 | 335/817 | chrX | 70451886 | ||
| chrX:70451895
|
A | C | 1 | a0004c0005 | 1 | NA18959.hp1 | synonymous_variant | LOW | c.1014A>C | p.Ile338Ile | DLG3 | ENSG00000082458.12 | transcript | ENST00000374360.8 | protein_coding | 7/19 | 1381/6042 | 1014/2454 | 338/817 | chrX | 70451895 | ||
| chrX:70492242
|
C | T | 1 | a0001c0007 | 1 | HG00438.hp1 | synonymous_variant | LOW | c.1656C>T | p.His552His | DLG3 | ENSG00000082458.12 | transcript | ENST00000374360.8 | protein_coding | 11/19 | 2023/6042 | 1656/2454 | 552/817 | chrX | 70492242 | ||
| chrX:70500940
|
C | A | 1 | a0001c0002 | 6 | HG01167.hp1 HG01169.hp1 HG02486.hp1 others(3): Show |
synonymous_variant | LOW | c.2298C>A | p.Ile766Ile | DLG3 | ENSG00000082458.12 | transcript | ENST00000374360.8 | protein_coding | 18/19 | 2665/6042 | 2298/2454 | 766/817 | chrX | 70500940 |
| 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:70444893
|
T | TC | 1 | a0001c0001t0013 | 1 | NA19076.hp1 | 5_prime_UTR_variant | MODIFIER | c.-308dupC | DLG3 | ENSG00000082458.12 | transcript | ENST00000374360.8 | protein_coding | 1/19 | 307 | INFO_REALIGN_3_PRIME | chrX | 70444893 | ||||
| chrX:70444912
|
C | CT | 1 | a0008c0010t0031 | 1 | NA18989.hp1 | 5_prime_UTR_variant | MODIFIER | c.-288dupT | DLG3 | ENSG00000082458.12 | transcript | ENST00000374360.8 | protein_coding | 1/19 | 287 | INFO_REALIGN_3_PRIME | chrX | 70444912 | ||||
| chrX:70444975
|
A | AG | 1 | a0001c0001t0013 | 1 | NA19076.hp1 | 5_prime_UTR_variant | MODIFIER | c.-222dupG | DLG3 | ENSG00000082458.12 | transcript | ENST00000374360.8 | protein_coding | 1/19 | 221 | INFO_REALIGN_3_PRIME | chrX | 70444975 | ||||
| chrX:70445000
|
C | CTG | 1 | a0008c0010t0031 | 1 | NA18989.hp1 | 5_prime_UTR_variant | MODIFIER | c.-202_-201insTG | DLG3 | ENSG00000082458.12 | transcript | ENST00000374360.8 | protein_coding | 1/19 | 201 | chrX | 70445000 | |||||
| chrX:70445002
|
T | TG | 1 | a0008c0010t0031 | 1 | NA18989.hp1 | 5_prime_UTR_variant | MODIFIER | c.-195dupG | DLG3 | ENSG00000082458.12 | transcript | ENST00000374360.8 | protein_coding | 1/19 | 194 | INFO_REALIGN_3_PRIME | chrX | 70445002 | ||||
| chrX:70445011
|
A | AG | 1 | a0008c0010t0031 | 1 | NA18989.hp1 | 5_prime_UTR_variant | MODIFIER | c.-189dupG | DLG3 | ENSG00000082458.12 | transcript | ENST00000374360.8 | protein_coding | 1/19 | 188 | INFO_REALIGN_3_PRIME | chrX | 70445011 | ||||
| chrX:70445039
|
G | GC | 1 | a0008c0010t0031 | 1 | NA18989.hp1 | 5_prime_UTR_variant | MODIFIER | c.-159dupC | DLG3 | ENSG00000082458.12 | transcript | ENST00000374360.8 | protein_coding | 1/19 | 158 | INFO_REALIGN_3_PRIME | chrX | 70445039 | ||||
| chrX:70445052
|
C | CG | 1 | a0001c0001t0013 | 1 | NA19076.hp1 | 5_prime_UTR_variant | MODIFIER | c.-147dupG | DLG3 | ENSG00000082458.12 | transcript | ENST00000374360.8 | protein_coding | 1/19 | 146 | INFO_REALIGN_3_PRIME | chrX | 70445052 | ||||
| chrX:70445069
|
G | GC | 4 | a0001c0001t0010a0001c0001t0013a0001c0001t0014others(1): Show | 6 | HG01192.hp1 HG02738.hp1 HG03831.hp1 others(3): Show |
5_prime_UTR_variant | MODIFIER | c.-125dupC | DLG3 | ENSG00000082458.12 | transcript | ENST00000374360.8 | protein_coding | 1/19 | 124 | INFO_REALIGN_3_PRIME | chrX | 70445069 | ||||
| chrX:70445111
|
GC | G | 1 | a0008c0010t0031 | 1 | NA18989.hp1 | 5_prime_UTR_variant | MODIFIER | c.-88delC | DLG3 | ENSG00000082458.12 | transcript | ENST00000374360.8 | protein_coding | 1/19 | 88 | INFO_REALIGN_3_PRIME | chrX | 70445111 | ||||
| chrX:70445113
|
C | CCGGCGG | 1 | a0001c0001t0007 | 4 | HG02280.hp2 HG02559.hp1 HG02559.hp2 others(1): Show |
5_prime_UTR_variant | MODIFIER | c.-76_-71dupCGGCGG | DLG3 | ENSG00000082458.12 | transcript | ENST00000374360.8 | protein_coding | 1/19 | 70 | INFO_REALIGN_3_PRIME | chrX | 70445113 | ||||
| chrX:70445113
|
CCGGCGGC others(5): Show |
C | 1 | a0001c0001t0009 | 4 | HG01123.hp1 HG01257.hp1 HG01258.hp1 others(1): Show |
5_prime_UTR_variant | MODIFIER | c.-82_-71delCGGCGGCG others(4): Show |
DLG3 | ENSG00000082458.12 | transcript | ENST00000374360.8 | protein_coding | 1/19 | 71 | INFO_REALIGN_3_PRIME | chrX | 70445113 | ||||
| chrX:70445132
|
T | C | 1 | a0001c0001t0011 | 3 | HG03540.hp2 HG06807.hp2 NA20300.hp1 |
5_prime_UTR_variant | MODIFIER | c.-70T>C | DLG3 | ENSG00000082458.12 | transcript | ENST00000374360.8 | protein_coding | 1/19 | 70 | chrX | 70445132 | |||||
| chrX:70445132
|
T | TG | 1 | a0008c0010t0031 | 1 | NA18989.hp1 | 5_prime_UTR_variant | MODIFIER | c.-68dupG | DLG3 | ENSG00000082458.12 | transcript | ENST00000374360.8 | protein_coding | 1/19 | 67 | INFO_REALIGN_3_PRIME | chrX | 70445132 | ||||
| chrX:70445172
|
T | TG | 1 | a0001c0001t0017 | 1 | HG01261.hp1 | 5_prime_UTR_variant | MODIFIER | c.-24dupG | DLG3 | ENSG00000082458.12 | transcript | ENST00000374360.8 | protein_coding | 1/19 | 23 | INFO_REALIGN_3_PRIME | chrX | 70445172 | ||||
| chrX:70445177
|
G | A | 1 | a0001c0001t0016 | 1 | HG03688.hp1 | 5_prime_UTR_variant | MODIFIER | c.-25G>A | DLG3 | ENSG00000082458.12 | transcript | ENST00000374360.8 | protein_coding | 1/19 | 25 | chrX | 70445177 | |||||
| chrX:70445180
|
C | CT | 1 | a0008c0010t0031 | 1 | NA18989.hp1 | 5_prime_UTR_variant | MODIFIER | c.-22_-21insT | DLG3 | ENSG00000082458.12 | transcript | ENST00000374360.8 | protein_coding | 1/19 | 21 | chrX | 70445180 | |||||
| chrX:70445188
|
C | CG | 2 | a0001c0001t0030a0008c0010t0031 | 2 | HG03927.hp2 NA18989.hp1 |
5_prime_UTR_variant | MODIFIER | c.-8dupG | DLG3 | ENSG00000082458.12 | transcript | ENST00000374360.8 | protein_coding | 1/19 | 7 | INFO_REALIGN_3_PRIME | chrX | 70445188 | ||||
| chrX:70502424
|
CT | C | 2 | a0001c0001t0008a0001c0001t0018 | 5 | NA18942.hp1 NA18994.hp1 NA19002.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*168delT | DLG3 | ENSG00000082458.12 | transcript | ENST00000374360.8 | protein_coding | 19/19 | 168 | INFO_REALIGN_3_PRIME | chrX | 70502424 | ||||
| chrX:70502586
|
T | G | 1 | a0001c0001t0004 | 7 | HG02055.hp1 HG02257.hp2 HG02922.hp1 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*317T>G | DLG3 | ENSG00000082458.12 | transcript | ENST00000374360.8 | protein_coding | 19/19 | 317 | chrX | 70502586 | |||||
| chrX:70502805
|
T | TTA | 1 | a0001c0001t0019 | 1 | NA19030.hp1 | 3_prime_UTR_variant | MODIFIER | c.*548_*549dupAT | DLG3 | ENSG00000082458.12 | transcript | ENST00000374360.8 | protein_coding | 19/19 | 550 | INFO_REALIGN_3_PRIME | chrX | 70502805 | ||||
| chrX:70502805
|
TTA | T | 1 | a0001c0001t0029 | 1 | HG02970.hp2 | 3_prime_UTR_variant | MODIFIER | c.*548_*549delAT | DLG3 | ENSG00000082458.12 | transcript | ENST00000374360.8 | protein_coding | 19/19 | 548 | INFO_REALIGN_3_PRIME | chrX | 70502805 | ||||
| chrX:70502824
|
ACT | A | 1 | a0001c0001t0020 | 1 | HG02886.hp1 | 3_prime_UTR_variant | MODIFIER | c.*559_*560delTC | DLG3 | ENSG00000082458.12 | transcript | ENST00000374360.8 | protein_coding | 19/19 | 559 | INFO_REALIGN_3_PRIME | chrX | 70502824 | ||||
| chrX:70503053
|
G | A | 1 | a0001c0001t0021 | 1 | NA19085.hp1 | 3_prime_UTR_variant | MODIFIER | c.*784G>A | DLG3 | ENSG00000082458.12 | transcript | ENST00000374360.8 | protein_coding | 19/19 | 784 | chrX | 70503053 | |||||
| chrX:70503548
|
C | T | 1 | a0006c0006t0015 | 1 | NA18949.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1279C>T | DLG3 | ENSG00000082458.12 | transcript | ENST00000374360.8 | protein_coding | 19/19 | 1279 | chrX | 70503548 | |||||
| chrX:70503597
|
G | GT | 4 | a0001c0001t0006a0001c0001t0018a0001c0001t0027others(1): Show | 8 | HG02145.hp1 HG03669.hp2 HG04115.hp1 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*1341dupT | DLG3 | ENSG00000082458.12 | transcript | ENST00000374360.8 | protein_coding | 19/19 | 1342 | INFO_REALIGN_3_PRIME | chrX | 70503597 | ||||
| chrX:70503597
|
GT | G | 1 | a0001c0001t0013 | 1 | NA19076.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1341delT | DLG3 | ENSG00000082458.12 | transcript | ENST00000374360.8 | protein_coding | 19/19 | 1341 | INFO_REALIGN_3_PRIME | chrX | 70503597 | ||||
| chrX:70503602
|
T | A | 1 | a0001c0001t0022 | 1 | HG02886.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1333T>A | DLG3 | ENSG00000082458.12 | transcript | ENST00000374360.8 | protein_coding | 19/19 | 1333 | chrX | 70503602 | |||||
| chrX:70503771
|
T | C | 1 | a0001c0001t0023 | 1 | HG03942.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1502T>C | DLG3 | ENSG00000082458.12 | transcript | ENST00000374360.8 | protein_coding | 19/19 | 1502 | chrX | 70503771 | |||||
| chrX:70503835
|
T | TC | 4 | a0001c0001t0005a0001c0001t0026a0001c0001t0028others(1): Show | 9 | HG01167.hp1 HG01169.hp1 HG01891.hp1 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*1574dupC | DLG3 | ENSG00000082458.12 | transcript | ENST00000374360.8 | protein_coding | 19/19 | 1575 | INFO_REALIGN_3_PRIME | chrX | 70503835 | ||||
| chrX:70504037
|
T | A | 1 | a0001c0001t0012 | 3 | HG00733.hp1 NA20752.hp1 homoSapiens_chm13v2.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1768T>A | DLG3 | ENSG00000082458.12 | transcript | ENST00000374360.8 | protein_coding | 19/19 | 1768 | chrX | 70504037 | |||||
| chrX:70504244
|
G | A | 24 | a0001c0001t0001a0001c0001t0005a0001c0001t0007others(21): Show | 144 | HG00621.hp1 HG00733.hp1 HG00735.hp1 others(141): Show |
3_prime_UTR_variant | MODIFIER | c.*1975G>A | DLG3 | ENSG00000082458.12 | transcript | ENST00000374360.8 | protein_coding | 19/19 | 1975 | chrX | 70504244 | |||||
| chrX:70504881
|
G | T | 25 | a0001c0001t0001a0001c0001t0003a0001c0001t0005others(22): Show | 156 | HG00099.hp1 HG00621.hp1 HG00642.hp1 others(153): Show |
3_prime_UTR_variant | MODIFIER | c.*2612G>T | DLG3 | ENSG00000082458.12 | transcript | ENST00000374360.8 | protein_coding | 19/19 | 2612 | chrX | 70504881 | |||||
| chrX:70505182
|
G | A | 2 | a0001c0001t0024a0001c0001t0027 | 2 | HG01081.hp2 NA18906.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2913G>A | DLG3 | ENSG00000082458.12 | transcript | ENST00000374360.8 | protein_coding | 19/19 | 2913 | chrX | 70505182 | |||||
| chrX:70505261
|
C | T | 1 | a0001c0001t0025 | 1 | HG02717.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2992C>T | DLG3 | ENSG00000082458.12 | transcript | ENST00000374360.8 | protein_coding | 19/19 | 2992 | chrX | 70505261 | |||||
| chrX:70505333
|
G | A | 1 | a0001c0001t0026 | 1 | HG03927.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3064G>A | DLG3 | ENSG00000082458.12 | transcript | ENST00000374360.8 | protein_coding | 19/19 | 3064 | chrX | 70505333 |
| 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:70445573
|
A | AG | 3 | a0001c0001t0002g0247a0001c0001t0030g0248a0002c0003t0001g0246 | 3 | HG03927.hp2 NA19058.hp1 NA19083.hp1 |
intron_variant | MODIFIER | c.357+21dupG | DLG3 | ENSG00000082458.12 | transcript | ENST00000374360.8 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chrX | 70445573 | |||||
| chrX:70445573
|
A | AGG | 1 | a0001c0001t0001g0249 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.357+20_357+21dupGG | DLG3 | ENSG00000082458.12 | transcript | ENST00000374360.8 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chrX | 70445573 | |||||
| chrX:70445582
|
C | CG | 1 | a0002c0003t0001g0246 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.357+26dupG | DLG3 | ENSG00000082458.12 | transcript | ENST00000374360.8 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chrX | 70445582 | |||||
| chrX:70445611
|
T | TG | 1 | a0008c0010t0031g0245 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.357+58dupG | DLG3 | ENSG00000082458.12 | transcript | ENST00000374360.8 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chrX | 70445611 | |||||
| chrX:70445673
|
G | GC | 1 | a0008c0010t0031g0245 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.357+118dupC | DLG3 | ENSG00000082458.12 | transcript | ENST00000374360.8 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chrX | 70445673 | |||||
| chrX:70445778
|
A | AG | 1 | a0002c0003t0001g0246 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.357+225dupG | DLG3 | ENSG00000082458.12 | transcript | ENST00000374360.8 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chrX | 70445778 | |||||
| chrX:70445798
|
A | AG | 1 | a0008c0010t0031g0245 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.357+244dupG | DLG3 | ENSG00000082458.12 | transcript | ENST00000374360.8 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chrX | 70445798 | |||||
| chrX:70445872
|
A | AG | 2 | a0001c0001t0013g0244a0008c0010t0031g0245 | 2 | NA18989.hp1 NA19076.hp1 |
intron_variant | MODIFIER | c.357+319dupG | DLG3 | ENSG00000082458.12 | transcript | ENST00000374360.8 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chrX | 70445872 | |||||
| chrX:70445899
|
T | TG | 1 | a0008c0010t0031g0245 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.357+342dupG | DLG3 | ENSG00000082458.12 | transcript | ENST00000374360.8 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chrX | 70445899 | |||||
| chrX:70445927
|
A | AG | 1 | a0002c0003t0001g0246 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.357+373dupG | DLG3 | ENSG00000082458.12 | transcript | ENST00000374360.8 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chrX | 70445927 | |||||
| chrX:70445927
|
AG | A | 1 | a0001c0001t0001g0249 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.357+373delG | DLG3 | ENSG00000082458.12 | transcript | ENST00000374360.8 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chrX | 70445927 | |||||
| chrX:70445953
|
A | AG | 1 | a0001c0001t0013g0244 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.357+401dupG | DLG3 | ENSG00000082458.12 | transcript | ENST00000374360.8 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chrX | 70445953 | |||||
| chrX:70446003
|
A | G | 24 | a0001c0001t0001g0017a0001c0001t0001g0224a0001c0001t0001g0225others(21): Show | 25 | HG01884.hp1 HG01891.hp2 HG02055.hp1 others(22): Show |
intron_variant | MODIFIER | c.357+445A>G | DLG3 | ENSG00000082458.12 | transcript | ENST00000374360.8 | protein_coding | 1/18 | chrX | 70446003 | ||||||
| chrX:70446048
|
C | T | 1 | a0001c0001t0002g0220 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.357+490C>T | DLG3 | ENSG00000082458.12 | transcript | ENST00000374360.8 | protein_coding | 1/18 | chrX | 70446048 | ||||||
| chrX:70446060
|
T | TC | 1 | a0008c0010t0031g0245 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.357+505dupC | DLG3 | ENSG00000082458.12 | transcript | ENST00000374360.8 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chrX | 70446060 | |||||
| chrX:70446153
|
T | TC | 1 | a0008c0010t0031g0245 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.357+596dupC | DLG3 | ENSG00000082458.12 | transcript | ENST00000374360.8 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chrX | 70446153 | |||||
| chrX:70446195
|
TG | T | 1 | a0002c0003t0001g0246 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.357+639delG | DLG3 | ENSG00000082458.12 | transcript | ENST00000374360.8 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chrX | 70446195 | |||||
| chrX:70446223
|
T | TG | 1 | a0008c0010t0031g0245 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.357+667dupG | DLG3 | ENSG00000082458.12 | transcript | ENST00000374360.8 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chrX | 70446223 | |||||
| chrX:70446225
|
G | GC | 1 | a0001c0001t0001g0249 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.357+668dupC | DLG3 | ENSG00000082458.12 | transcript | ENST00000374360.8 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chrX | 70446225 | |||||
| chrX:70446244
|
G | A | 1 | a0001c0001t0021g0018 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.357+686G>A | DLG3 | ENSG00000082458.12 | transcript | ENST00000374360.8 | protein_coding | 1/18 | chrX | 70446244 | ||||||
| chrX:70446272
|
T | TTG | 1 | a0008c0010t0031g0245 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.357+714_357+715ins others(2): Show |
DLG3 | ENSG00000082458.12 | transcript | ENST00000374360.8 | protein_coding | 1/18 | chrX | 70446272 | ||||||
| chrX:70446273
|
G | T | 1 | a0008c0010t0031g0245 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.357+715G>T | DLG3 | ENSG00000082458.12 | transcript | ENST00000374360.8 | protein_coding | 1/18 | chrX | 70446273 | ||||||
| chrX:70446280
|
T | TG | 1 | a0008c0010t0031g0245 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.357+723dupG | DLG3 | ENSG00000082458.12 | transcript | ENST00000374360.8 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chrX | 70446280 | |||||
| chrX:70446283
|
G | GT | 1 | a0008c0010t0031g0245 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.357+727dupT | DLG3 | ENSG00000082458.12 | transcript | ENST00000374360.8 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chrX | 70446283 | |||||
| chrX:70446417
|
C | CG | 1 | a0001c0001t0002g0247 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.357+863dupG | DLG3 | ENSG00000082458.12 | transcript | ENST00000374360.8 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chrX | 70446417 | |||||
| chrX:70446430
|
C | CG | 1 | a0001c0001t0001g0219 | 1 | HG03492.hp1 | intron_variant | MODIFIER | c.357+878dupG | DLG3 | ENSG00000082458.12 | transcript | ENST00000374360.8 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chrX | 70446430 | |||||
| chrX:70446430
|
CG | C | 1 | a0001c0001t0001g0249 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.357+878delG | DLG3 | ENSG00000082458.12 | transcript | ENST00000374360.8 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chrX | 70446430 | |||||
| chrX:70446437
|
C | CG | 1 | a0002c0003t0001g0246 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.357+885dupG | DLG3 | ENSG00000082458.12 | transcript | ENST00000374360.8 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chrX | 70446437 | |||||
| chrX:70446437
|
C | G | 1 | a0008c0010t0031g0245 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.357+879C>G | DLG3 | ENSG00000082458.12 | transcript | ENST00000374360.8 | protein_coding | 1/18 | chrX | 70446437 | ||||||
| chrX:70446438
|
G | GGC | 1 | a0008c0010t0031g0245 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.357+881_357+882ins others(2): Show |
DLG3 | ENSG00000082458.12 | transcript | ENST00000374360.8 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chrX | 70446438 | |||||
| chrX:70446480
|
G | C | 1 | a0001c0001t0001g0019 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.357+922G>C | DLG3 | ENSG00000082458.12 | transcript | ENST00000374360.8 | protein_coding | 1/18 | chrX | 70446480 | ||||||
| chrX:70446570
|
G | GT | 1 | a0002c0003t0001g0246 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.357+1012_357+1013i others(3): Show |
DLG3 | ENSG00000082458.12 | transcript | ENST00000374360.8 | protein_coding | 1/18 | chrX | 70446570 | ||||||
| chrX:70446623
|
T | TG | 1 | a0008c0010t0031g0245 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.357+1068dupG | DLG3 | ENSG00000082458.12 | transcript | ENST00000374360.8 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chrX | 70446623 | |||||
| chrX:70446687
|
A | AG | 1 | a0002c0003t0001g0246 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.357+1130dupG | DLG3 | ENSG00000082458.12 | transcript | ENST00000374360.8 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chrX | 70446687 | |||||
| chrX:70446747
|
G | T | 1 | a0001c0001t0020g0218 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.357+1189G>T | DLG3 | ENSG00000082458.12 | transcript | ENST00000374360.8 | protein_coding | 1/18 | chrX | 70446747 | ||||||
| chrX:70446756
|
A | AGG | 1 | a0008c0010t0031g0245 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.357+1200_357+1201d others(4): Show |
DLG3 | ENSG00000082458.12 | transcript | ENST00000374360.8 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chrX | 70446756 | |||||
| chrX:70446789
|
T | A | 1 | a0001c0001t0001g0020 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.357+1231T>A | DLG3 | ENSG00000082458.12 | transcript | ENST00000374360.8 | protein_coding | 1/18 | chrX | 70446789 | ||||||
| chrX:70446794
|
T | TG | 1 | a0002c0003t0001g0246 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.357+1240dupG | DLG3 | ENSG00000082458.12 | transcript | ENST00000374360.8 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chrX | 70446794 | |||||
| chrX:70446797
|
G | GGT | 1 | a0008c0010t0031g0245 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.357+1240_357+1241i others(4): Show |
DLG3 | ENSG00000082458.12 | transcript | ENST00000374360.8 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chrX | 70446797 | |||||
| chrX:70446798
|
G | C | 8 | a0001c0001t0001g0021a0001c0001t0001g0022a0001c0001t0001g0224others(5): Show | 8 | HG01884.hp1 HG02055.hp1 HG02109.hp1 others(5): Show |
intron_variant | MODIFIER | c.357+1240G>C | DLG3 | ENSG00000082458.12 | transcript | ENST00000374360.8 | protein_coding | 1/18 | chrX | 70446798 | ||||||
| chrX:70446926
|
TG | T | 1 | a0001c0001t0013g0244 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.357+1372delG | DLG3 | ENSG00000082458.12 | transcript | ENST00000374360.8 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chrX | 70446926 | |||||
| chrX:70446962
|
T | TC | 1 | a0008c0010t0031g0245 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.357+1406dupC | DLG3 | ENSG00000082458.12 | transcript | ENST00000374360.8 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chrX | 70446962 | |||||
| chrX:70447008
|
T | C | 2 | a0001c0001t0001g0023a0001c0001t0001g0024 | 2 | NA18950.hp2 NA19005.hp1 |
intron_variant | MODIFIER | c.357+1450T>C | DLG3 | ENSG00000082458.12 | transcript | ENST00000374360.8 | protein_coding | 1/18 | chrX | 70447008 | ||||||
| chrX:70447050
|
TG | T | 1 | a0008c0010t0031g0245 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.357+1494delG | DLG3 | ENSG00000082458.12 | transcript | ENST00000374360.8 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chrX | 70447050 | |||||
| chrX:70447057
|
CT | C | 1 | a0008c0010t0031g0245 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.357+1502delT | DLG3 | ENSG00000082458.12 | transcript | ENST00000374360.8 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chrX | 70447057 | |||||
| chrX:70447065
|
C | T | 49 | a0001c0001t0001g0017a0001c0001t0001g0019a0001c0001t0001g0020others(46): Show | 50 | HG00621.hp1 HG00735.hp1 HG00738.hp1 others(47): Show |
intron_variant | MODIFIER | c.357+1507C>T | DLG3 | ENSG00000082458.12 | transcript | ENST00000374360.8 | protein_coding | 1/18 | chrX | 70447065 | ||||||
| chrX:70447066
|
G | C | 1 | a0001c0001t0001g0025 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.357+1508G>C | DLG3 | ENSG00000082458.12 | transcript | ENST00000374360.8 | protein_coding | 1/18 | chrX | 70447066 | ||||||
| chrX:70447094
|
CG | C | 1 | a0008c0010t0031g0245 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.357+1538delG | DLG3 | ENSG00000082458.12 | transcript | ENST00000374360.8 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chrX | 70447094 | |||||
| chrX:70447159
|
T | TCC | 1 | a0002c0003t0001g0246 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.357+1603_357+1604d others(4): Show |
DLG3 | ENSG00000082458.12 | transcript | ENST00000374360.8 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chrX | 70447159 | |||||
| chrX:70447244
|
TG | T | 1 | a0002c0003t0001g0246 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.358-1666delG | DLG3 | ENSG00000082458.12 | transcript | ENST00000374360.8 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chrX | 70447244 | |||||
| chrX:70447305
|
C | CA | 1 | a0002c0003t0001g0246 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.358-1605dupA | DLG3 | ENSG00000082458.12 | transcript | ENST00000374360.8 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chrX | 70447305 | |||||
| chrX:70447346
|
T | C | 1 | a0001c0001t0001g0026 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.358-1567T>C | DLG3 | ENSG00000082458.12 | transcript | ENST00000374360.8 | protein_coding | 1/18 | chrX | 70447346 | ||||||
| chrX:70447385
|
G | A | 1 | a0001c0001t0002g0027 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.358-1528G>A | DLG3 | ENSG00000082458.12 | transcript | ENST00000374360.8 | protein_coding | 1/18 | chrX | 70447385 | ||||||
| chrX:70447606
|
G | GC | 1 | a0008c0010t0031g0245 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.358-1302dupC | DLG3 | ENSG00000082458.12 | transcript | ENST00000374360.8 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chrX | 70447606 | |||||
| chrX:70447618
|
G | GT | 1 | a0008c0010t0031g0245 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.358-1292dupT | DLG3 | ENSG00000082458.12 | transcript | ENST00000374360.8 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chrX | 70447618 | |||||
| chrX:70447655
|
T | G | 1 | a0001c0001t0013g0244 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.358-1258T>G | DLG3 | ENSG00000082458.12 | transcript | ENST00000374360.8 | protein_coding | 1/18 | chrX | 70447655 | ||||||
| chrX:70447656
|
C | G | 1 | a0001c0001t0013g0244 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.358-1257C>G | DLG3 | ENSG00000082458.12 | transcript | ENST00000374360.8 | protein_coding | 1/18 | chrX | 70447656 | ||||||
| chrX:70447680
|
GA | G | 1 | a0008c0010t0031g0245 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.358-1230delA | DLG3 | ENSG00000082458.12 | transcript | ENST00000374360.8 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chrX | 70447680 | |||||
| chrX:70447725
|
A | AG | 1 | a0008c0010t0031g0245 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.358-1185dupG | DLG3 | ENSG00000082458.12 | transcript | ENST00000374360.8 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chrX | 70447725 | |||||
| chrX:70447802
|
C | CA | 1 | a0002c0003t0001g0246 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.358-1111_358-1110i others(3): Show |
DLG3 | ENSG00000082458.12 | transcript | ENST00000374360.8 | protein_coding | 1/18 | chrX | 70447802 | ||||||
| chrX:70447851
|
G | GCCA | 2 | a0001c0001t0001g0182a0001c0001t0001g0237 | 2 | HG02109.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.358-1062_358-1061i others(5): Show |
DLG3 | ENSG00000082458.12 | transcript | ENST00000374360.8 | protein_coding | 1/18 | chrX | 70447851 | ||||||
| chrX:70447878
|
A | AC | 1 | a0002c0003t0001g0246 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.358-1031dupC | DLG3 | ENSG00000082458.12 | transcript | ENST00000374360.8 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chrX | 70447878 | |||||
| chrX:70447928
|
G | GA | 1 | a0008c0010t0031g0245 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.358-984dupA | DLG3 | ENSG00000082458.12 | transcript | ENST00000374360.8 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chrX | 70447928 | |||||
| chrX:70447952
|
G | GT | 1 | a0008c0010t0031g0245 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.358-961_358-960ins others(1): Show |
DLG3 | ENSG00000082458.12 | transcript | ENST00000374360.8 | protein_coding | 1/18 | chrX | 70447952 | ||||||
| chrX:70447965
|
T | C | 18 | a0001c0001t0001g0029a0001c0001t0001g0038a0001c0001t0003g0008others(15): Show | 19 | HG00099.hp1 HG00642.hp1 HG00733.hp2 others(16): Show |
intron_variant | MODIFIER | c.358-948T>C | DLG3 | ENSG00000082458.12 | transcript | ENST00000374360.8 | protein_coding | 1/18 | chrX | 70447965 | ||||||
| chrX:70447999
|
T | TC | 1 | a0008c0010t0031g0245 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.358-911dupC | DLG3 | ENSG00000082458.12 | transcript | ENST00000374360.8 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chrX | 70447999 | |||||
| chrX:70448039
|
A | AC | 1 | a0008c0010t0031g0245 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.358-871dupC | DLG3 | ENSG00000082458.12 | transcript | ENST00000374360.8 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chrX | 70448039 | |||||
| chrX:70448063
|
A | C | 20 | a0001c0001t0001g0026a0001c0001t0001g0029a0001c0001t0001g0038others(17): Show | 21 | HG00099.hp1 HG00642.hp1 HG00733.hp2 others(18): Show |
intron_variant | MODIFIER | c.358-850A>C | DLG3 | ENSG00000082458.12 | transcript | ENST00000374360.8 | protein_coding | 1/18 | chrX | 70448063 | ||||||
| chrX:70448140
|
T | TG | 1 | a0008c0010t0031g0245 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.358-770dupG | DLG3 | ENSG00000082458.12 | transcript | ENST00000374360.8 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chrX | 70448140 | |||||
| chrX:70448203
|
C | T | 3 | a0001c0001t0001g0179a0001c0001t0001g0180a0001c0001t0001g0217 | 3 | HG01358.hp1 HG01516.hp2 HG01517.hp1 |
intron_variant | MODIFIER | c.358-710C>T | DLG3 | ENSG00000082458.12 | transcript | ENST00000374360.8 | protein_coding | 1/18 | chrX | 70448203 | ||||||
| chrX:70448241
|
G | GA | 1 | a0002c0003t0001g0246 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.358-672_358-671ins others(1): Show |
DLG3 | ENSG00000082458.12 | transcript | ENST00000374360.8 | protein_coding | 1/18 | chrX | 70448241 | ||||||
| chrX:70448299
|
G | A | 17 | a0001c0001t0001g0026a0001c0001t0001g0044a0001c0001t0001g0045others(14): Show | 17 | HG01081.hp2 HG02451.hp1 HG02559.hp1 others(14): Show |
intron_variant | MODIFIER | c.358-614G>A | DLG3 | ENSG00000082458.12 | transcript | ENST00000374360.8 | protein_coding | 1/18 | chrX | 70448299 | ||||||
| chrX:70448340
|
A | T | 1 | a0001c0001t0007g0178 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.358-573A>T | DLG3 | ENSG00000082458.12 | transcript | ENST00000374360.8 | protein_coding | 1/18 | chrX | 70448340 | ||||||
| chrX:70448400
|
G | A | 1 | a0001c0001t0001g0053 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.358-513G>A | DLG3 | ENSG00000082458.12 | transcript | ENST00000374360.8 | protein_coding | 1/18 | chrX | 70448400 | ||||||
| chrX:70448431
|
G | A | 2 | a0001c0001t0002g0054a0001c0001t0014g0055 | 2 | HG03831.hp1 NA18984.hp1 |
intron_variant | MODIFIER | c.358-482G>A | DLG3 | ENSG00000082458.12 | transcript | ENST00000374360.8 | protein_coding | 1/18 | chrX | 70448431 | ||||||
| chrX:70448452
|
T | TC | 1 | a0008c0010t0031g0245 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.358-456dupC | DLG3 | ENSG00000082458.12 | transcript | ENST00000374360.8 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chrX | 70448452 | |||||
| chrX:70448520
|
T | TA | 1 | a0008c0010t0031g0245 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.358-392dupA | DLG3 | ENSG00000082458.12 | transcript | ENST00000374360.8 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chrX | 70448520 | |||||
| chrX:70448570
|
T | TC | 1 | a0008c0010t0031g0245 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.358-338dupC | DLG3 | ENSG00000082458.12 | transcript | ENST00000374360.8 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chrX | 70448570 | |||||
| chrX:70448605
|
A | AC | 1 | a0008c0010t0031g0245 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.358-305dupC | DLG3 | ENSG00000082458.12 | transcript | ENST00000374360.8 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chrX | 70448605 | |||||
| chrX:70448613
|
A | G | 150 | a0001c0001t0001g0015a0001c0001t0001g0016a0001c0001t0001g0017others(147): Show | 158 | HG00099.hp1 HG00621.hp1 HG00642.hp1 others(155): Show |
intron_variant | MODIFIER | c.358-300A>G | DLG3 | ENSG00000082458.12 | transcript | ENST00000374360.8 | protein_coding | 1/18 | chrX | 70448613 | ||||||
| chrX:70448618
|
G | A | 1 | a0001c0001t0001g0133 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.358-295G>A | DLG3 | ENSG00000082458.12 | transcript | ENST00000374360.8 | protein_coding | 1/18 | chrX | 70448618 | ||||||
| chrX:70448748
|
G | C | 1 | a0001c0001t0011g0043 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.358-165G>C | DLG3 | ENSG00000082458.12 | transcript | ENST00000374360.8 | protein_coding | 1/18 | chrX | 70448748 | ||||||
| chrX:70448751
|
GC | G | 1 | a0008c0010t0031g0245 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.358-160delC | DLG3 | ENSG00000082458.12 | transcript | ENST00000374360.8 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chrX | 70448751 | |||||
| chrX:70448993
|
G | GA | 1 | a0008c0010t0031g0245 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.408+30_408+31insA | DLG3 | ENSG00000082458.12 | transcript | ENST00000374360.8 | protein_coding | 2/18 | chrX | 70448993 | ||||||
| chrX:70448997
|
A | AG | 1 | a0008c0010t0031g0245 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.408+36dupG | DLG3 | ENSG00000082458.12 | transcript | ENST00000374360.8 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chrX | 70448997 | |||||
| chrX:70449022
|
G | C | 1 | a0001c0001t0004g0181 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.408+59G>C | DLG3 | ENSG00000082458.12 | transcript | ENST00000374360.8 | protein_coding | 2/18 | chrX | 70449022 | ||||||
| chrX:70449053
|
TG | T | 1 | a0001c0001t0002g0056 | 1 | NA18957.hp2 | intron_variant | MODIFIER | c.408+96delG | DLG3 | ENSG00000082458.12 | transcript | ENST00000374360.8 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chrX | 70449053 | |||||
| chrX:70449143
|
T | C | 1 | a0001c0001t0012g0006 | 3 | HG00733.hp1 NA20752.hp1 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.408+180T>C | DLG3 | ENSG00000082458.12 | transcript | ENST00000374360.8 | protein_coding | 2/18 | chrX | 70449143 | ||||||
| chrX:70449502
|
A | AG | 1 | a0002c0003t0001g0246 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.533+22dupG | DLG3 | ENSG00000082458.12 | transcript | ENST00000374360.8 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chrX | 70449502 | |||||
| chrX:70449513
|
TG | T | 1 | a0008c0010t0031g0245 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.533+32delG | DLG3 | ENSG00000082458.12 | transcript | ENST00000374360.8 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chrX | 70449513 | |||||
| chrX:70449550
|
G | GC | 1 | a0008c0010t0031g0245 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.533+69dupC | DLG3 | ENSG00000082458.12 | transcript | ENST00000374360.8 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chrX | 70449550 | |||||
| chrX:70449596
|
G | T | 1 | a0008c0010t0031g0245 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.534-94G>T | DLG3 | ENSG00000082458.12 | transcript | ENST00000374360.8 | protein_coding | 3/18 | chrX | 70449596 | ||||||
| chrX:70449598
|
C | G | 1 | a0008c0010t0031g0245 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.534-92C>G | DLG3 | ENSG00000082458.12 | transcript | ENST00000374360.8 | protein_coding | 3/18 | chrX | 70449598 | ||||||
| chrX:70449600
|
G | GGC | 1 | a0008c0010t0031g0245 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.534-90_534-89insGC | DLG3 | ENSG00000082458.12 | transcript | ENST00000374360.8 | protein_coding | 3/18 | chrX | 70449600 | ||||||
| chrX:70449652
|
A | AG | 1 | a0008c0010t0031g0245 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.534-34dupG | DLG3 | ENSG00000082458.12 | transcript | ENST00000374360.8 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chrX | 70449652 | |||||
| chrX:70450331
|
C | T | 3 | a0001c0001t0001g0177a0001c0001t0009g0007a0001c0001t0009g0176 | 5 | HG01109.hp1 HG01123.hp1 HG01257.hp1 others(2): Show |
intron_variant | MODIFIER | c.840+26C>T | DLG3 | ENSG00000082458.12 | transcript | ENST00000374360.8 | protein_coding | 5/18 | chrX | 70450331 | ||||||
| chrX:70450400
|
C | CA | 1 | a0008c0010t0031g0245 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.840+96dupA | DLG3 | ENSG00000082458.12 | transcript | ENST00000374360.8 | protein_coding | 5/18 | INFO_REALIGN_3_PRIME | chrX | 70450400 | |||||
| chrX:70450427
|
A | C | 1 | a0001c0001t0001g0026 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.840+122A>C | DLG3 | ENSG00000082458.12 | transcript | ENST00000374360.8 | protein_coding | 5/18 | chrX | 70450427 | ||||||
| chrX:70450441
|
T | TG | 1 | a0008c0010t0031g0245 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.840+137dupG | DLG3 | ENSG00000082458.12 | transcript | ENST00000374360.8 | protein_coding | 5/18 | INFO_REALIGN_3_PRIME | chrX | 70450441 | |||||
| chrX:70450462
|
A | T | 19 | a0001c0001t0001g0044a0001c0001t0001g0045a0001c0001t0001g0046others(16): Show | 19 | HG01081.hp2 HG01255.hp1 HG02280.hp2 others(16): Show |
intron_variant | MODIFIER | c.840+157A>T | DLG3 | ENSG00000082458.12 | transcript | ENST00000374360.8 | protein_coding | 5/18 | chrX | 70450462 | ||||||
| chrX:70450603
|
CT | C | 1 | a0002c0003t0001g0246 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.841-34delT | DLG3 | ENSG00000082458.12 | transcript | ENST00000374360.8 | protein_coding | 5/18 | INFO_REALIGN_3_PRIME | chrX | 70450603 | |||||
| chrX:70450815
|
A | AT | 1 | a0002c0003t0001g0246 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.985+32_985+33insT | DLG3 | ENSG00000082458.12 | transcript | ENST00000374360.8 | protein_coding | 6/18 | chrX | 70450815 | ||||||
| chrX:70450981
|
C | CATAGAGT others(11): Show |
1 | a0002c0003t0001g0246 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.985+201_985+218dup others(18): Show |
DLG3 | ENSG00000082458.12 | transcript | ENST00000374360.8 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chrX | 70450981 | |||||
| chrX:70450994
|
T | C | 3 | a0001c0001t0001g0044a0001c0001t0001g0134a0001c0001t0001g0219 | 3 | HG03041.hp2 HG03491.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.985+211T>C | DLG3 | ENSG00000082458.12 | transcript | ENST00000374360.8 | protein_coding | 6/18 | chrX | 70450994 | ||||||
| chrX:70451031
|
TA | T | 1 | a0001c0001t0002g0132 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.985+253delA | DLG3 | ENSG00000082458.12 | transcript | ENST00000374360.8 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chrX | 70451031 | |||||
| chrX:70451101
|
G | GT | 1 | a0007c0004t0002g0131 | 1 | NA18972.hp2 | intron_variant | MODIFIER | c.985+325dupT | DLG3 | ENSG00000082458.12 | transcript | ENST00000374360.8 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chrX | 70451101 | |||||
| chrX:70451115
|
T | G | 1 | a0001c0001t0001g0023 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.985+332T>G | DLG3 | ENSG00000082458.12 | transcript | ENST00000374360.8 | protein_coding | 6/18 | chrX | 70451115 | ||||||
| chrX:70451140
|
T | TC | 1 | a0001c0001t0002g0132 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.985+358dupC | DLG3 | ENSG00000082458.12 | transcript | ENST00000374360.8 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chrX | 70451140 | |||||
| chrX:70451208
|
TCTC | T | 3 | a0001c0001t0011g0043a0001c0001t0024g0052a0001c0001t0027g0051 | 3 | HG01081.hp2 NA18906.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.985+428_985+430del others(3): Show |
DLG3 | ENSG00000082458.12 | transcript | ENST00000374360.8 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chrX | 70451208 | |||||
| chrX:70451227
|
G | A | 1 | a0001c0001t0001g0185 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.985+444G>A | DLG3 | ENSG00000082458.12 | transcript | ENST00000374360.8 | protein_coding | 6/18 | chrX | 70451227 | ||||||
| chrX:70451291
|
C | T | 1 | a0001c0001t0001g0053 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.985+508C>T | DLG3 | ENSG00000082458.12 | transcript | ENST00000374360.8 | protein_coding | 6/18 | chrX | 70451291 | ||||||
| chrX:70451555
|
TG | T | 2 | a0001c0001t0002g0132a0002c0003t0001g0246 | 2 | NA19056.hp1 NA19058.hp1 |
intron_variant | MODIFIER | c.986-310delG | DLG3 | ENSG00000082458.12 | transcript | ENST00000374360.8 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chrX | 70451555 | |||||
| chrX:70451585
|
AG | A | 1 | a0002c0003t0001g0246 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.986-279delG | DLG3 | ENSG00000082458.12 | transcript | ENST00000374360.8 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chrX | 70451585 | |||||
| chrX:70451752
|
A | G | 31 | a0001c0001t0001g0015a0001c0001t0001g0016a0001c0001t0001g0025others(28): Show | 35 | HG01109.hp1 HG01123.hp1 HG01257.hp1 others(32): Show |
intron_variant | MODIFIER | c.986-115A>G | DLG3 | ENSG00000082458.12 | transcript | ENST00000374360.8 | protein_coding | 6/18 | chrX | 70451752 | ||||||
| chrX:70451800
|
C | G | 6 | a0001c0001t0001g0021a0001c0001t0001g0022a0001c0001t0001g0224others(3): Show | 6 | HG01884.hp1 HG02109.hp1 HG02145.hp1 others(3): Show |
intron_variant | MODIFIER | c.986-67C>G | DLG3 | ENSG00000082458.12 | transcript | ENST00000374360.8 | protein_coding | 6/18 | chrX | 70451800 | ||||||
| chrX:70451812
|
T | TG | 1 | a0008c0010t0031g0245 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.986-51dupG | DLG3 | ENSG00000082458.12 | transcript | ENST00000374360.8 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chrX | 70451812 | |||||
| chrX:70451849
|
TC | T | 1 | a0005c0008t0002g0129 | 1 | NA18988.hp1 | intron_variant | MODIFIER | c.986-15delC | DLG3 | ENSG00000082458.12 | transcript | ENST00000374360.8 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chrX | 70451849 | |||||
| chrX:70451850
|
C | G | 1 | a0004c0005t0001g0172 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.986-17C>G | DLG3 | ENSG00000082458.12 | transcript | ENST00000374360.8 | protein_coding | 6/18 | chrX | 70451850 | ||||||
| chrX:70451851
|
C | T | 1 | a0004c0005t0001g0172 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.986-16C>T | DLG3 | ENSG00000082458.12 | transcript | ENST00000374360.8 | protein_coding | 6/18 | chrX | 70451851 | ||||||
| chrX:70451855
|
T | G | 1 | a0004c0005t0001g0172 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.986-12T>G | DLG3 | ENSG00000082458.12 | transcript | ENST00000374360.8 | protein_coding | 6/18 | chrX | 70451855 | ||||||
| chrX:70451856
|
C | A | 1 | a0004c0005t0001g0172 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.986-11C>A | DLG3 | ENSG00000082458.12 | transcript | ENST00000374360.8 | protein_coding | 6/18 | chrX | 70451856 | ||||||
| chrX:70451858
|
T | TA | 1 | a0004c0005t0001g0172 | 1 | NA18959.hp1 | splice_region_variant&intron_variant | LOW | c.986-9_986-8insA | DLG3 | ENSG00000082458.12 | transcript | ENST00000374360.8 | protein_coding | 6/18 | chrX | 70451858 | ||||||
| chrX:70451861
|
T | G | 1 | a0004c0005t0001g0172 | 1 | NA18959.hp1 | splice_region_variant&intron_variant | LOW | c.986-6T>G | DLG3 | ENSG00000082458.12 | transcript | ENST00000374360.8 | protein_coding | 6/18 | chrX | 70451861 | ||||||
| chrX:70451863
|
C | T | 1 | a0004c0005t0001g0172 | 1 | NA18959.hp1 | splice_region_variant&intron_variant | LOW | c.986-4C>T | DLG3 | ENSG00000082458.12 | transcript | ENST00000374360.8 | protein_coding | 6/18 | chrX | 70451863 | ||||||
| chrX:70451864
|
C | A | 1 | a0004c0005t0001g0172 | 1 | NA18959.hp1 | splice_region_variant&intron_variant | LOW | c.986-3C>A | DLG3 | ENSG00000082458.12 | transcript | ENST00000374360.8 | protein_coding | 6/18 | chrX | 70451864 | ||||||
| chrX:70451865
|
A | G | 1 | a0004c0005t0001g0172 | 1 | NA18959.hp1 | splice_acceptor_variant&intron_variant | HIGH | c.986-2A>G | DLG3 | ENSG00000082458.12 | transcript | ENST00000374360.8 | protein_coding | 6/18 | chrX | 70451865 | ||||||
| chrX:70452070
|
TG | T | 1 | a0002c0003t0001g0246 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.1145+48delG | DLG3 | ENSG00000082458.12 | transcript | ENST00000374360.8 | protein_coding | 7/18 | INFO_REALIGN_3_PRIME | chrX | 70452070 | |||||
| chrX:70452149
|
TC | T | 1 | a0005c0008t0002g0129 | 1 | NA18988.hp1 | intron_variant | MODIFIER | c.1145+126delC | DLG3 | ENSG00000082458.12 | transcript | ENST00000374360.8 | protein_coding | 7/18 | INFO_REALIGN_3_PRIME | chrX | 70452149 | |||||
| chrX:70452256
|
GC | G | 1 | a0001c0001t0001g0171 | 1 | NA18993.hp2 | intron_variant | MODIFIER | c.1145+234delC | DLG3 | ENSG00000082458.12 | transcript | ENST00000374360.8 | protein_coding | 7/18 | INFO_REALIGN_3_PRIME | chrX | 70452256 | |||||
| chrX:70452331
|
G | A | 1 | a0001c0001t0010g0186 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.1145+305G>A | DLG3 | ENSG00000082458.12 | transcript | ENST00000374360.8 | protein_coding | 7/18 | chrX | 70452331 | ||||||
| chrX:70452493
|
C | T | 1 | a0001c0001t0002g0014 | 2 | HG00140.hp1 HG01081.hp1 |
intron_variant | MODIFIER | c.1145+467C>T | DLG3 | ENSG00000082458.12 | transcript | ENST00000374360.8 | protein_coding | 7/18 | chrX | 70452493 | ||||||
| chrX:70452501
|
GGAACT | G | 1 | a0001c0001t0001g0171 | 1 | NA18993.hp2 | intron_variant | MODIFIER | c.1145+477_1145+481d others(7): Show |
DLG3 | ENSG00000082458.12 | transcript | ENST00000374360.8 | protein_coding | 7/18 | INFO_REALIGN_3_PRIME | chrX | 70452501 | |||||
| chrX:70452527
|
CG | C | 1 | a0001c0001t0002g0132 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.1145+506delG | DLG3 | ENSG00000082458.12 | transcript | ENST00000374360.8 | protein_coding | 7/18 | INFO_REALIGN_3_PRIME | chrX | 70452527 | |||||
| chrX:70452540
|
T | TG | 1 | a0001c0001t0001g0171 | 1 | NA18993.hp2 | intron_variant | MODIFIER | c.1145+515dupG | DLG3 | ENSG00000082458.12 | transcript | ENST00000374360.8 | protein_coding | 7/18 | INFO_REALIGN_3_PRIME | chrX | 70452540 | |||||
| chrX:70452551
|
G | GC | 1 | a0006c0006t0015g0057 | 1 | NA18949.hp1 | intron_variant | MODIFIER | c.1145+528dupC | DLG3 | ENSG00000082458.12 | transcript | ENST00000374360.8 | protein_coding | 7/18 | INFO_REALIGN_3_PRIME | chrX | 70452551 | |||||
| chrX:70452562
|
TG | T | 1 | a0001c0001t0001g0171 | 1 | NA18993.hp2 | intron_variant | MODIFIER | c.1145+538delG | DLG3 | ENSG00000082458.12 | transcript | ENST00000374360.8 | protein_coding | 7/18 | INFO_REALIGN_3_PRIME | chrX | 70452562 | |||||
| chrX:70452605
|
G | GGA | 2 | a0001c0001t0002g0060a0001c0001t0006g0143 | 2 | HG01346.hp2 HG04115.hp1 |
intron_variant | MODIFIER | c.1145+589_1145+590d others(4): Show |
DLG3 | ENSG00000082458.12 | transcript | ENST00000374360.8 | protein_coding | 7/18 | INFO_REALIGN_3_PRIME | chrX | 70452605 | |||||
| chrX:70452612
|
G | C | 98 | a0001c0001t0001g0015a0001c0001t0001g0016a0001c0001t0001g0017others(95): Show | 105 | HG00621.hp1 HG00733.hp1 HG00735.hp1 others(102): Show |
intron_variant | MODIFIER | c.1145+586G>C | DLG3 | ENSG00000082458.12 | transcript | ENST00000374360.8 | protein_coding | 7/18 | chrX | 70452612 | ||||||
| chrX:70452741
|
C | T | 1 | a0001c0001t0002g0128 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.1145+715C>T | DLG3 | ENSG00000082458.12 | transcript | ENST00000374360.8 | protein_coding | 7/18 | chrX | 70452741 | ||||||
| chrX:70452787
|
C | CG | 1 | a0005c0008t0002g0129 | 1 | NA18988.hp1 | intron_variant | MODIFIER | c.1145+764dupG | DLG3 | ENSG00000082458.12 | transcript | ENST00000374360.8 | protein_coding | 7/18 | INFO_REALIGN_3_PRIME | chrX | 70452787 | |||||
| chrX:70452805
|
T | C | 153 | a0001c0001t0001g0015a0001c0001t0001g0016a0001c0001t0001g0017others(150): Show | 162 | HG00099.hp1 HG00621.hp1 HG00642.hp1 others(159): Show |
intron_variant | MODIFIER | c.1145+779T>C | DLG3 | ENSG00000082458.12 | transcript | ENST00000374360.8 | protein_coding | 7/18 | chrX | 70452805 | ||||||
| chrX:70452846
|
G | T | 1 | a0001c0007t0002g0127 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.1146-791G>T | DLG3 | ENSG00000082458.12 | transcript | ENST00000374360.8 | protein_coding | 7/18 | chrX | 70452846 | ||||||
| chrX:70452847
|
TG | T | 1 | a0006c0006t0015g0057 | 1 | NA18949.hp1 | intron_variant | MODIFIER | c.1146-786delG | DLG3 | ENSG00000082458.12 | transcript | ENST00000374360.8 | protein_coding | 7/18 | INFO_REALIGN_3_PRIME | chrX | 70452847 | |||||
| chrX:70452971
|
T | C | 1 | a0001c0001t0002g0064 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.1146-666T>C | DLG3 | ENSG00000082458.12 | transcript | ENST00000374360.8 | protein_coding | 7/18 | chrX | 70452971 | ||||||
| chrX:70453129
|
TAGGA | T | 1 | a0001c0001t0007g0050 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.1146-507_1146-504d others(6): Show |
DLG3 | ENSG00000082458.12 | transcript | ENST00000374360.8 | protein_coding | 7/18 | chrX | 70453129 | ||||||
| chrX:70453148
|
TG | T | 1 | a0001c0001t0001g0171 | 1 | NA18993.hp2 | intron_variant | MODIFIER | c.1146-486delG | DLG3 | ENSG00000082458.12 | transcript | ENST00000374360.8 | protein_coding | 7/18 | INFO_REALIGN_3_PRIME | chrX | 70453148 | |||||
| chrX:70453198
|
ATCCTG | A | 1 | a0002c0003t0001g0246 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.1146-437_1146-433d others(7): Show |
DLG3 | ENSG00000082458.12 | transcript | ENST00000374360.8 | protein_coding | 7/18 | INFO_REALIGN_3_PRIME | chrX | 70453198 | |||||
| chrX:70453216
|
G | GC | 1 | a0005c0008t0002g0129 | 1 | NA18988.hp1 | intron_variant | MODIFIER | c.1146-420dupC | DLG3 | ENSG00000082458.12 | transcript | ENST00000374360.8 | protein_coding | 7/18 | INFO_REALIGN_3_PRIME | chrX | 70453216 | |||||
| chrX:70453295
|
G | A | 1 | a0001c0001t0001g0187 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.1146-342G>A | DLG3 | ENSG00000082458.12 | transcript | ENST00000374360.8 | protein_coding | 7/18 | chrX | 70453295 | ||||||
| chrX:70453402
|
T | TGGGAAGT others(15): Show |
11 | a0001c0001t0001g0044a0001c0001t0001g0045a0001c0001t0001g0046others(8): Show | 11 | HG02451.hp1 HG02559.hp1 HG02572.hp1 others(8): Show |
intron_variant | MODIFIER | c.1146-228_1146-207d others(24): Show |
DLG3 | ENSG00000082458.12 | transcript | ENST00000374360.8 | protein_coding | 7/18 | INFO_REALIGN_3_PRIME | chrX | 70453402 | |||||
| chrX:70453541
|
TC | T | 1 | a0005c0008t0002g0129 | 1 | NA18988.hp1 | intron_variant | MODIFIER | c.1146-93delC | DLG3 | ENSG00000082458.12 | transcript | ENST00000374360.8 | protein_coding | 7/18 | INFO_REALIGN_3_PRIME | chrX | 70453541 | |||||
| chrX:70453547
|
C | T | 1 | a0001c0001t0002g0126 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.1146-90C>T | DLG3 | ENSG00000082458.12 | transcript | ENST00000374360.8 | protein_coding | 7/18 | chrX | 70453547 | ||||||
| chrX:70453614
|
C | T | 17 | a0001c0001t0001g0029a0001c0001t0001g0038a0001c0001t0003g0008others(14): Show | 18 | HG00099.hp1 HG00642.hp1 HG00733.hp2 others(15): Show |
intron_variant | MODIFIER | c.1146-23C>T | DLG3 | ENSG00000082458.12 | transcript | ENST00000374360.8 | protein_coding | 7/18 | chrX | 70453614 | ||||||
| chrX:70453628
|
TC | T | 1 | a0005c0008t0002g0129 | 1 | NA18988.hp1 | splice_region_variant&intron_variant | LOW | c.1146-6delC | DLG3 | ENSG00000082458.12 | transcript | ENST00000374360.8 | protein_coding | 7/18 | INFO_REALIGN_3_PRIME | chrX | 70453628 | |||||
| chrX:70453867
|
C | T | 1 | a0001c0001t0001g0142 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.1302+74C>T | DLG3 | ENSG00000082458.12 | transcript | ENST00000374360.8 | protein_coding | 8/18 | chrX | 70453867 | ||||||
| chrX:70453908
|
TG | T | 1 | a0004c0005t0001g0172 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.1302+117delG | DLG3 | ENSG00000082458.12 | transcript | ENST00000374360.8 | protein_coding | 8/18 | INFO_REALIGN_3_PRIME | chrX | 70453908 | |||||
| chrX:70453961
|
T | C | 156 | a0001c0001t0001g0015a0001c0001t0001g0016a0001c0001t0001g0017others(153): Show | 165 | HG00099.hp1 HG00621.hp1 HG00642.hp1 others(162): Show |
intron_variant | MODIFIER | c.1302+168T>C | DLG3 | ENSG00000082458.12 | transcript | ENST00000374360.8 | protein_coding | 8/18 | chrX | 70453961 | ||||||
| chrX:70454052
|
T | G | 42 | a0001c0001t0001g0019a0001c0001t0001g0023a0001c0001t0001g0024others(39): Show | 43 | HG00621.hp1 HG00738.hp1 HG01261.hp1 others(40): Show |
intron_variant | MODIFIER | c.1303-162T>G | DLG3 | ENSG00000082458.12 | transcript | ENST00000374360.8 | protein_coding | 8/18 | chrX | 70454052 | ||||||
| chrX:70454065
|
AG | A | 1 | a0004c0005t0001g0172 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.1303-147delG | DLG3 | ENSG00000082458.12 | transcript | ENST00000374360.8 | protein_coding | 8/18 | INFO_REALIGN_3_PRIME | chrX | 70454065 | |||||
| chrX:70454096
|
TG | T | 1 | a0004c0005t0001g0172 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.1303-115delG | DLG3 | ENSG00000082458.12 | transcript | ENST00000374360.8 | protein_coding | 8/18 | INFO_REALIGN_3_PRIME | chrX | 70454096 | |||||
| chrX:70454333
|
TG | T | 1 | a0006c0006t0015g0057 | 1 | NA18949.hp1 | intron_variant | MODIFIER | c.1405+20delG | DLG3 | ENSG00000082458.12 | transcript | ENST00000374360.8 | protein_coding | 9/18 | INFO_REALIGN_3_PRIME | chrX | 70454333 | |||||
| chrX:70454361
|
CTTATA | C | 1 | a0001c0001t0026g0136 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.1405+50_1405+54del others(5): Show |
DLG3 | ENSG00000082458.12 | transcript | ENST00000374360.8 | protein_coding | 9/18 | INFO_REALIGN_3_PRIME | chrX | 70454361 | |||||
| chrX:70454452
|
C | CT | 1 | a0006c0006t0015g0057 | 1 | NA18949.hp1 | intron_variant | MODIFIER | c.1405+140dupT | DLG3 | ENSG00000082458.12 | transcript | ENST00000374360.8 | protein_coding | 9/18 | INFO_REALIGN_3_PRIME | chrX | 70454452 | |||||
| chrX:70454475
|
GT | G | 1 | a0004c0005t0001g0172 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.1405+162delT | DLG3 | ENSG00000082458.12 | transcript | ENST00000374360.8 | protein_coding | 9/18 | INFO_REALIGN_3_PRIME | chrX | 70454475 | |||||
| chrX:70454612
|
AG | A | 1 | a0006c0006t0015g0057 | 1 | NA18949.hp1 | intron_variant | MODIFIER | c.1405+301delG | DLG3 | ENSG00000082458.12 | transcript | ENST00000374360.8 | protein_coding | 9/18 | INFO_REALIGN_3_PRIME | chrX | 70454612 | |||||
| chrX:70454643
|
G | GA | 1 | a0006c0006t0015g0057 | 1 | NA18949.hp1 | intron_variant | MODIFIER | c.1405+329dupA | DLG3 | ENSG00000082458.12 | transcript | ENST00000374360.8 | protein_coding | 9/18 | INFO_REALIGN_3_PRIME | chrX | 70454643 | |||||
| chrX:70454652
|
GC | G | 1 | a0004c0005t0001g0172 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.1405+339delC | DLG3 | ENSG00000082458.12 | transcript | ENST00000374360.8 | protein_coding | 9/18 | INFO_REALIGN_3_PRIME | chrX | 70454652 | |||||
| chrX:70454655
|
C | T | 1 | a0001c0001t0011g0043 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.1405+339C>T | DLG3 | ENSG00000082458.12 | transcript | ENST00000374360.8 | protein_coding | 9/18 | chrX | 70454655 | ||||||
| chrX:70454765
|
A | G | 6 | a0001c0002t0005g0039a0001c0002t0005g0040a0001c0002t0005g0041others(3): Show | 6 | HG01167.hp1 HG01169.hp1 HG02486.hp1 others(3): Show |
intron_variant | MODIFIER | c.1405+449A>G | DLG3 | ENSG00000082458.12 | transcript | ENST00000374360.8 | protein_coding | 9/18 | chrX | 70454765 | ||||||
| chrX:70454789
|
C | A | 1 | a0003c0009t0002g0065 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.1405+473C>A | DLG3 | ENSG00000082458.12 | transcript | ENST00000374360.8 | protein_coding | 9/18 | chrX | 70454789 | ||||||
| chrX:70454844
|
TC | T | 1 | a0008c0010t0031g0245 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.1405+532delC | DLG3 | ENSG00000082458.12 | transcript | ENST00000374360.8 | protein_coding | 9/18 | INFO_REALIGN_3_PRIME | chrX | 70454844 | |||||
| chrX:70455135
|
T | TC | 2 | a0001c0001t0010g0154a0002c0003t0001g0246 | 2 | HG02738.hp1 NA19058.hp1 |
intron_variant | MODIFIER | c.1405+824dupC | DLG3 | ENSG00000082458.12 | transcript | ENST00000374360.8 | protein_coding | 9/18 | INFO_REALIGN_3_PRIME | chrX | 70455135 | |||||
| chrX:70455277
|
G | T | 1 | a0001c0001t0023g0203 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.1405+961G>T | DLG3 | ENSG00000082458.12 | transcript | ENST00000374360.8 | protein_coding | 9/18 | chrX | 70455277 | ||||||
| chrX:70455294
|
C | T | 1 | a0001c0001t0002g0125 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.1405+978C>T | DLG3 | ENSG00000082458.12 | transcript | ENST00000374360.8 | protein_coding | 9/18 | chrX | 70455294 | ||||||
| chrX:70455301
|
T | TC | 2 | a0001c0001t0010g0154a0001c0001t0016g0066 | 2 | HG02738.hp1 HG03688.hp1 |
intron_variant | MODIFIER | c.1405+991dupC | DLG3 | ENSG00000082458.12 | transcript | ENST00000374360.8 | protein_coding | 9/18 | INFO_REALIGN_3_PRIME | chrX | 70455301 | |||||
| chrX:70455330
|
T | G | 1 | a0001c0001t0001g0026 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1405+1014T>G | DLG3 | ENSG00000082458.12 | transcript | ENST00000374360.8 | protein_coding | 9/18 | chrX | 70455330 | ||||||
| chrX:70455472
|
TG | T | 1 | a0008c0010t0031g0245 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.1405+1159delG | DLG3 | ENSG00000082458.12 | transcript | ENST00000374360.8 | protein_coding | 9/18 | INFO_REALIGN_3_PRIME | chrX | 70455472 | |||||
| chrX:70455521
|
G | T | 1 | a0001c0001t0022g0227 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.1405+1205G>T | DLG3 | ENSG00000082458.12 | transcript | ENST00000374360.8 | protein_coding | 9/18 | chrX | 70455521 | ||||||
| chrX:70455891
|
G | C | 1 | a0001c0001t0011g0043 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.1405+1575G>C | DLG3 | ENSG00000082458.12 | transcript | ENST00000374360.8 | protein_coding | 9/18 | chrX | 70455891 | ||||||
| chrX:70455985
|
G | GC | 1 | a0006c0006t0015g0057 | 1 | NA18949.hp1 | intron_variant | MODIFIER | c.1405+1671dupC | DLG3 | ENSG00000082458.12 | transcript | ENST00000374360.8 | protein_coding | 9/18 | INFO_REALIGN_3_PRIME | chrX | 70455985 | |||||
| chrX:70456178
|
GA | G | 1 | a0008c0010t0031g0245 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.1405+1864delA | DLG3 | ENSG00000082458.12 | transcript | ENST00000374360.8 | protein_coding | 9/18 | INFO_REALIGN_3_PRIME | chrX | 70456178 | |||||
| chrX:70456198
|
G | GT | 1 | a0006c0006t0015g0057 | 1 | NA18949.hp1 | intron_variant | MODIFIER | c.1405+1889dupT | DLG3 | ENSG00000082458.12 | transcript | ENST00000374360.8 | protein_coding | 9/18 | INFO_REALIGN_3_PRIME | chrX | 70456198 | |||||
| chrX:70456382
|
G | A | 1 | a0001c0001t0001g0155 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.1405+2066G>A | DLG3 | ENSG00000082458.12 | transcript | ENST00000374360.8 | protein_coding | 9/18 | chrX | 70456382 | ||||||
| chrX:70456436
|
TG | T | 1 | a0006c0006t0015g0057 | 1 | NA18949.hp1 | intron_variant | MODIFIER | c.1405+2125delG | DLG3 | ENSG00000082458.12 | transcript | ENST00000374360.8 | protein_coding | 9/18 | INFO_REALIGN_3_PRIME | chrX | 70456436 | |||||
| chrX:70456482
|
AG | A | 1 | a0008c0010t0031g0245 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.1405+2170delG | DLG3 | ENSG00000082458.12 | transcript | ENST00000374360.8 | protein_coding | 9/18 | INFO_REALIGN_3_PRIME | chrX | 70456482 | |||||
| chrX:70456710
|
C | CT | 1 | a0006c0006t0015g0057 | 1 | NA18949.hp1 | intron_variant | MODIFIER | c.1405+2397dupT | DLG3 | ENSG00000082458.12 | transcript | ENST00000374360.8 | protein_coding | 9/18 | INFO_REALIGN_3_PRIME | chrX | 70456710 | |||||
| chrX:70456713
|
TG | T | 1 | a0004c0005t0001g0172 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.1405+2399delG | DLG3 | ENSG00000082458.12 | transcript | ENST00000374360.8 | protein_coding | 9/18 | INFO_REALIGN_3_PRIME | chrX | 70456713 | |||||
| chrX:70456751
|
C | CT | 4 | a0001c0001t0001g0026a0001c0001t0006g0124a0001c0001t0022g0227others(1): Show | 4 | HG02886.hp2 NA18949.hp1 NA18991.hp1 others(1): Show |
intron_variant | MODIFIER | c.1405+2447dupT | DLG3 | ENSG00000082458.12 | transcript | ENST00000374360.8 | protein_coding | 9/18 | INFO_REALIGN_3_PRIME | chrX | 70456751 | |||||
| chrX:70456751
|
CT | C | 15 | a0001c0001t0001g0029a0001c0001t0001g0038a0001c0001t0001g0204others(12): Show | 16 | HG00099.hp1 HG00642.hp1 HG00733.hp2 others(13): Show |
intron_variant | MODIFIER | c.1405+2447delT | DLG3 | ENSG00000082458.12 | transcript | ENST00000374360.8 | protein_coding | 9/18 | INFO_REALIGN_3_PRIME | chrX | 70456751 | |||||
| chrX:70456763
|
T | C | 1 | a0001c0001t0002g0067 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.1405+2447T>C | DLG3 | ENSG00000082458.12 | transcript | ENST00000374360.8 | protein_coding | 9/18 | chrX | 70456763 | ||||||
| chrX:70456854
|
GT | G | 1 | a0008c0010t0031g0245 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.1405+2543delT | DLG3 | ENSG00000082458.12 | transcript | ENST00000374360.8 | protein_coding | 9/18 | INFO_REALIGN_3_PRIME | chrX | 70456854 | |||||
| chrX:70456859
|
TA | T | 2 | a0004c0005t0001g0172a0006c0006t0015g0057 | 2 | NA18949.hp1 NA18959.hp1 |
intron_variant | MODIFIER | c.1405+2548delA | DLG3 | ENSG00000082458.12 | transcript | ENST00000374360.8 | protein_coding | 9/18 | INFO_REALIGN_3_PRIME | chrX | 70456859 | |||||
| chrX:70456894
|
C | T | 147 | a0001c0001t0001g0015a0001c0001t0001g0016a0001c0001t0001g0017others(144): Show | 155 | HG00099.hp1 HG00621.hp1 HG00642.hp1 others(152): Show |
intron_variant | MODIFIER | c.1405+2578C>T | DLG3 | ENSG00000082458.12 | transcript | ENST00000374360.8 | protein_coding | 9/18 | chrX | 70456894 | ||||||
| chrX:70456950
|
C | G | 6 | a0001c0001t0002g0013a0001c0001t0002g0120a0001c0001t0002g0121others(3): Show | 7 | HG02135.hp1 NA18968.hp2 NA18971.hp1 others(4): Show |
intron_variant | MODIFIER | c.1405+2634C>G | DLG3 | ENSG00000082458.12 | transcript | ENST00000374360.8 | protein_coding | 9/18 | chrX | 70456950 | ||||||
| chrX:70457018
|
A | AT | 1 | a0006c0006t0015g0057 | 1 | NA18949.hp1 | intron_variant | MODIFIER | c.1405+2711dupT | DLG3 | ENSG00000082458.12 | transcript | ENST00000374360.8 | protein_coding | 9/18 | INFO_REALIGN_3_PRIME | chrX | 70457018 | |||||
| chrX:70457018
|
AT | A | 1 | a0004c0005t0001g0172 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.1405+2711delT | DLG3 | ENSG00000082458.12 | transcript | ENST00000374360.8 | protein_coding | 9/18 | INFO_REALIGN_3_PRIME | chrX | 70457018 | |||||
| chrX:70457106
|
C | G | 90 | a0001c0001t0001g0015a0001c0001t0001g0016a0001c0001t0001g0017others(87): Show | 97 | HG00621.hp1 HG00733.hp1 HG00735.hp1 others(94): Show |
intron_variant | MODIFIER | c.1405+2790C>G | DLG3 | ENSG00000082458.12 | transcript | ENST00000374360.8 | protein_coding | 9/18 | chrX | 70457106 | ||||||
| chrX:70457235
|
C | T | 1 | a0001c0001t0019g0141 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1405+2919C>T | DLG3 | ENSG00000082458.12 | transcript | ENST00000374360.8 | protein_coding | 9/18 | chrX | 70457235 | ||||||
| chrX:70457369
|
C | CT | 1 | a0006c0006t0015g0057 | 1 | NA18949.hp1 | intron_variant | MODIFIER | c.1405+3056dupT | DLG3 | ENSG00000082458.12 | transcript | ENST00000374360.8 | protein_coding | 9/18 | INFO_REALIGN_3_PRIME | chrX | 70457369 | |||||
| chrX:70457406
|
TA | T | 1 | a0004c0005t0001g0172 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.1405+3096delA | DLG3 | ENSG00000082458.12 | transcript | ENST00000374360.8 | protein_coding | 9/18 | INFO_REALIGN_3_PRIME | chrX | 70457406 | |||||
| chrX:70457456
|
C | CT | 1 | a0006c0006t0015g0057 | 1 | NA18949.hp1 | intron_variant | MODIFIER | c.1405+3145dupT | DLG3 | ENSG00000082458.12 | transcript | ENST00000374360.8 | protein_coding | 9/18 | INFO_REALIGN_3_PRIME | chrX | 70457456 | |||||
| chrX:70457470
|
GT | G | 1 | a0006c0006t0015g0057 | 1 | NA18949.hp1 | intron_variant | MODIFIER | c.1405+3156delT | DLG3 | ENSG00000082458.12 | transcript | ENST00000374360.8 | protein_coding | 9/18 | INFO_REALIGN_3_PRIME | chrX | 70457470 | |||||
| chrX:70457546
|
G | T | 1 | a0001c0001t0001g0243 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.1405+3230G>T | DLG3 | ENSG00000082458.12 | transcript | ENST00000374360.8 | protein_coding | 9/18 | chrX | 70457546 | ||||||
| chrX:70457574
|
C | CT | 42 | a0001c0001t0001g0019a0001c0001t0001g0023a0001c0001t0001g0024others(39): Show | 43 | HG00621.hp1 HG00738.hp1 HG01261.hp1 others(40): Show |
intron_variant | MODIFIER | c.1405+3273dupT | DLG3 | ENSG00000082458.12 | transcript | ENST00000374360.8 | protein_coding | 9/18 | INFO_REALIGN_3_PRIME | chrX | 70457574 | |||||
| chrX:70457574
|
CT | C | 3 | a0001c0001t0002g0068a0001c0001t0002g0069a0001c0001t0018g0070 | 3 | HG01257.hp2 HG02896.hp1 NA19063.hp1 |
intron_variant | MODIFIER | c.1405+3273delT | DLG3 | ENSG00000082458.12 | transcript | ENST00000374360.8 | protein_coding | 9/18 | INFO_REALIGN_3_PRIME | chrX | 70457574 | |||||
| chrX:70457594
|
C | T | 13 | a0001c0001t0001g0029a0001c0001t0001g0038a0001c0001t0001g0204others(10): Show | 14 | HG00099.hp1 HG00642.hp1 HG00733.hp2 others(11): Show |
intron_variant | MODIFIER | c.1405+3278C>T | DLG3 | ENSG00000082458.12 | transcript | ENST00000374360.8 | protein_coding | 9/18 | chrX | 70457594 | ||||||
| chrX:70457624
|
T | C | 1 | a0001c0001t0001g0026 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1405+3308T>C | DLG3 | ENSG00000082458.12 | transcript | ENST00000374360.8 | protein_coding | 9/18 | chrX | 70457624 | ||||||
| chrX:70457719
|
T | G | 1 | a0001c0001t0002g0064 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.1405+3403T>G | DLG3 | ENSG00000082458.12 | transcript | ENST00000374360.8 | protein_coding | 9/18 | chrX | 70457719 | ||||||
| chrX:70457728
|
C | T | 1 | a0001c0001t0001g0026 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1405+3412C>T | DLG3 | ENSG00000082458.12 | transcript | ENST00000374360.8 | protein_coding | 9/18 | chrX | 70457728 | ||||||
| chrX:70457790
|
C | T | 3 | a0001c0001t0001g0047a0001c0001t0001g0048a0001c0001t0001g0049 | 3 | HG02622.hp2 HG03130.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.1405+3474C>T | DLG3 | ENSG00000082458.12 | transcript | ENST00000374360.8 | protein_coding | 9/18 | chrX | 70457790 | ||||||
| chrX:70457849
|
G | GA | 1 | a0006c0006t0015g0057 | 1 | NA18949.hp1 | intron_variant | MODIFIER | c.1405+3534dupA | DLG3 | ENSG00000082458.12 | transcript | ENST00000374360.8 | protein_coding | 9/18 | INFO_REALIGN_3_PRIME | chrX | 70457849 | |||||
| chrX:70457866
|
CG | C | 1 | a0004c0005t0001g0172 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.1405+3552delG | DLG3 | ENSG00000082458.12 | transcript | ENST00000374360.8 | protein_coding | 9/18 | INFO_REALIGN_3_PRIME | chrX | 70457866 | |||||
| chrX:70457916
|
C | T | 7 | a0001c0001t0001g0044a0001c0001t0001g0045a0001c0001t0001g0046others(4): Show | 7 | HG02280.hp2 HG02451.hp1 HG02559.hp1 others(4): Show |
intron_variant | MODIFIER | c.1405+3600C>T | DLG3 | ENSG00000082458.12 | transcript | ENST00000374360.8 | protein_coding | 9/18 | chrX | 70457916 | ||||||
| chrX:70458120
|
C | T | 20 | a0001c0001t0001g0023a0001c0001t0001g0024a0001c0001t0001g0145others(17): Show | 20 | HG00738.hp1 HG01167.hp1 HG01169.hp1 others(17): Show |
intron_variant | MODIFIER | c.1405+3804C>T | DLG3 | ENSG00000082458.12 | transcript | ENST00000374360.8 | protein_coding | 9/18 | chrX | 70458120 | ||||||
| chrX:70458266
|
CCT | C | 1 | a0001c0001t0019g0141 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1405+3954_1405+395 others(6): Show |
DLG3 | ENSG00000082458.12 | transcript | ENST00000374360.8 | protein_coding | 9/18 | INFO_REALIGN_3_PRIME | chrX | 70458266 | |||||
| chrX:70458292
|
C | T | 13 | a0001c0001t0001g0029a0001c0001t0001g0038a0001c0001t0001g0204others(10): Show | 14 | HG00099.hp1 HG00642.hp1 HG00733.hp2 others(11): Show |
intron_variant | MODIFIER | c.1405+3976C>T | DLG3 | ENSG00000082458.12 | transcript | ENST00000374360.8 | protein_coding | 9/18 | chrX | 70458292 | ||||||
| chrX:70458295
|
G | A | 3 | a0001c0001t0001g0137a0001c0001t0001g0235a0001c0001t0001g0236 | 3 | HG03453.hp2 HG03471.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.1405+3979G>A | DLG3 | ENSG00000082458.12 | transcript | ENST00000374360.8 | protein_coding | 9/18 | chrX | 70458295 | ||||||
| chrX:70458305
|
A | G | 11 | a0001c0001t0001g0038a0001c0001t0003g0008a0001c0001t0003g0030others(8): Show | 12 | HG00099.hp1 HG00642.hp1 HG00733.hp2 others(9): Show |
intron_variant | MODIFIER | c.1405+3989A>G | DLG3 | ENSG00000082458.12 | transcript | ENST00000374360.8 | protein_coding | 9/18 | chrX | 70458305 | ||||||
| chrX:70458332
|
C | T | 1 | a0001c0001t0001g0226 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1405+4016C>T | DLG3 | ENSG00000082458.12 | transcript | ENST00000374360.8 | protein_coding | 9/18 | chrX | 70458332 | ||||||
| chrX:70458456
|
T | TATTTGTT others(1): Show |
1 | a0001c0001t0001g0049 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.1405+4145_1405+415 others(12): Show |
DLG3 | ENSG00000082458.12 | transcript | ENST00000374360.8 | protein_coding | 9/18 | INFO_REALIGN_3_PRIME | chrX | 70458456 | |||||
| chrX:70458475
|
A | G | 1 | a0001c0001t0001g0053 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.1405+4159A>G | DLG3 | ENSG00000082458.12 | transcript | ENST00000374360.8 | protein_coding | 9/18 | chrX | 70458475 | ||||||
| chrX:70458793
|
G | T | 42 | a0001c0001t0001g0019a0001c0001t0001g0023a0001c0001t0001g0024others(39): Show | 42 | HG00621.hp1 HG00738.hp1 HG01167.hp1 others(39): Show |
intron_variant | MODIFIER | c.1405+4477G>T | DLG3 | ENSG00000082458.12 | transcript | ENST00000374360.8 | protein_coding | 9/18 | chrX | 70458793 | ||||||
| chrX:70458838
|
ACCTAT | A | 1 | a0001c0001t0001g0049 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.1405+4523_1405+452 others(9): Show |
DLG3 | ENSG00000082458.12 | transcript | ENST00000374360.8 | protein_coding | 9/18 | chrX | 70458838 | ||||||
| chrX:70458845
|
AG | A | 1 | a0001c0001t0001g0049 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.1405+4530delG | DLG3 | ENSG00000082458.12 | transcript | ENST00000374360.8 | protein_coding | 9/18 | chrX | 70458845 | ||||||
| chrX:70458883
|
C | G | 5 | a0001c0001t0001g0022a0001c0001t0001g0224a0001c0001t0001g0225others(2): Show | 5 | HG01884.hp1 HG02109.hp1 HG02145.hp1 others(2): Show |
intron_variant | MODIFIER | c.1405+4567C>G | DLG3 | ENSG00000082458.12 | transcript | ENST00000374360.8 | protein_coding | 9/18 | chrX | 70458883 | ||||||
| chrX:70458937
|
T | TA | 1 | a0006c0006t0015g0057 | 1 | NA18949.hp1 | intron_variant | MODIFIER | c.1405+4625dupA | DLG3 | ENSG00000082458.12 | transcript | ENST00000374360.8 | protein_coding | 9/18 | INFO_REALIGN_3_PRIME | chrX | 70458937 | |||||
| chrX:70459042
|
TC | T | 1 | a0006c0006t0015g0057 | 1 | NA18949.hp1 | intron_variant | MODIFIER | c.1405+4730delC | DLG3 | ENSG00000082458.12 | transcript | ENST00000374360.8 | protein_coding | 9/18 | INFO_REALIGN_3_PRIME | chrX | 70459042 | |||||
| chrX:70459047
|
G | A | 1 | a0001c0001t0010g0186 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.1405+4731G>A | DLG3 | ENSG00000082458.12 | transcript | ENST00000374360.8 | protein_coding | 9/18 | chrX | 70459047 | ||||||
| chrX:70459064
|
G | A | 1 | a0001c0001t0001g0157 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.1405+4748G>A | DLG3 | ENSG00000082458.12 | transcript | ENST00000374360.8 | protein_coding | 9/18 | chrX | 70459064 | ||||||
| chrX:70459071
|
T | C | 2 | a0001c0001t0002g0071a0001c0001t0002g0072 | 2 | NA18962.hp1 NA19077.hp2 |
intron_variant | MODIFIER | c.1405+4755T>C | DLG3 | ENSG00000082458.12 | transcript | ENST00000374360.8 | protein_coding | 9/18 | chrX | 70459071 | ||||||
| chrX:70459232
|
TG | T | 1 | a0001c0001t0001g0152 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.1405+4921delG | DLG3 | ENSG00000082458.12 | transcript | ENST00000374360.8 | protein_coding | 9/18 | INFO_REALIGN_3_PRIME | chrX | 70459232 | |||||
| chrX:70459277
|
A | G | 38 | a0001c0001t0001g0019a0001c0001t0001g0023a0001c0001t0001g0024others(35): Show | 38 | HG00621.hp1 HG00738.hp1 HG01261.hp1 others(35): Show |
intron_variant | MODIFIER | c.1405+4961A>G | DLG3 | ENSG00000082458.12 | transcript | ENST00000374360.8 | protein_coding | 9/18 | chrX | 70459277 | ||||||
| chrX:70459301
|
C | CT | 1 | a0006c0006t0015g0057 | 1 | NA18949.hp1 | intron_variant | MODIFIER | c.1405+4989dupT | DLG3 | ENSG00000082458.12 | transcript | ENST00000374360.8 | protein_coding | 9/18 | INFO_REALIGN_3_PRIME | chrX | 70459301 | |||||
| chrX:70459357
|
T | A | 150 | a0001c0001t0001g0015a0001c0001t0001g0016a0001c0001t0001g0017others(147): Show | 158 | HG00099.hp1 HG00621.hp1 HG00642.hp1 others(155): Show |
intron_variant | MODIFIER | c.1405+5041T>A | DLG3 | ENSG00000082458.12 | transcript | ENST00000374360.8 | protein_coding | 9/18 | chrX | 70459357 | ||||||
| chrX:70459388
|
TC | T | 1 | a0001c0001t0008g0073 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.1405+5076delC | DLG3 | ENSG00000082458.12 | transcript | ENST00000374360.8 | protein_coding | 9/18 | INFO_REALIGN_3_PRIME | chrX | 70459388 | |||||
| chrX:70459405
|
T | TA | 1 | a0006c0006t0015g0057 | 1 | NA18949.hp1 | intron_variant | MODIFIER | c.1405+5091dupA | DLG3 | ENSG00000082458.12 | transcript | ENST00000374360.8 | protein_coding | 9/18 | INFO_REALIGN_3_PRIME | chrX | 70459405 | |||||
| chrX:70459638
|
TC | T | 1 | a0001c0001t0008g0073 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.1405+5326delC | DLG3 | ENSG00000082458.12 | transcript | ENST00000374360.8 | protein_coding | 9/18 | INFO_REALIGN_3_PRIME | chrX | 70459638 | |||||
| chrX:70459646
|
G | A | 2 | a0001c0001t0024g0052a0001c0001t0027g0051 | 2 | HG01081.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.1405+5330G>A | DLG3 | ENSG00000082458.12 | transcript | ENST00000374360.8 | protein_coding | 9/18 | chrX | 70459646 | ||||||
| chrX:70460053
|
G | A | 1 | a0001c0001t0029g0238 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.1405+5737G>A | DLG3 | ENSG00000082458.12 | transcript | ENST00000374360.8 | protein_coding | 9/18 | chrX | 70460053 | ||||||
| chrX:70460273
|
ACT | A | 1 | a0001c0001t0003g0156 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.1405+5960_1405+596 others(6): Show |
DLG3 | ENSG00000082458.12 | transcript | ENST00000374360.8 | protein_coding | 9/18 | INFO_REALIGN_3_PRIME | chrX | 70460273 | |||||
| chrX:70460282
|
C | CA | 37 | a0001c0001t0002g0001a0001c0001t0002g0013a0001c0001t0002g0054others(34): Show | 41 | HG00609.hp1 HG00673.hp1 HG00735.hp2 others(38): Show |
intron_variant | MODIFIER | c.1405+5991dupA | DLG3 | ENSG00000082458.12 | transcript | ENST00000374360.8 | protein_coding | 9/18 | INFO_REALIGN_3_PRIME | chrX | 70460282 | |||||
| chrX:70460282
|
C | CAA | 9 | a0001c0001t0002g0004a0001c0001t0002g0074a0001c0001t0002g0075others(6): Show | 11 | HG00438.hp1 HG00438.hp2 HG02027.hp1 others(8): Show |
intron_variant | MODIFIER | c.1405+5990_1405+599 others(6): Show |
DLG3 | ENSG00000082458.12 | transcript | ENST00000374360.8 | protein_coding | 9/18 | INFO_REALIGN_3_PRIME | chrX | 70460282 | |||||
| chrX:70460282
|
CA | C | 13 | a0001c0001t0001g0023a0001c0001t0001g0024a0001c0001t0001g0135others(10): Show | 13 | HG00738.hp1 HG01361.hp1 HG02630.hp2 others(10): Show |
intron_variant | MODIFIER | c.1405+5991delA | DLG3 | ENSG00000082458.12 | transcript | ENST00000374360.8 | protein_coding | 9/18 | INFO_REALIGN_3_PRIME | chrX | 70460282 | |||||
| chrX:70460282
|
CAA | C | 3 | a0001c0001t0004g0119a0001c0001t0004g0233a0001c0001t0004g0234 | 3 | HG02922.hp1 NA18906.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.1405+5990_1405+599 others(6): Show |
DLG3 | ENSG00000082458.12 | transcript | ENST00000374360.8 | protein_coding | 9/18 | INFO_REALIGN_3_PRIME | chrX | 70460282 | |||||
| chrX:70460284
|
A | G | 1 | a0001c0001t0001g0026 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1405+5968A>G | DLG3 | ENSG00000082458.12 | transcript | ENST00000374360.8 | protein_coding | 9/18 | chrX | 70460284 | ||||||
| chrX:70460292
|
A | C | 4 | a0001c0001t0001g0029a0001c0001t0001g0149a0001c0001t0001g0150others(1): Show | 4 | HG02280.hp1 NA19002.hp2 NA19011.hp1 others(1): Show |
intron_variant | MODIFIER | c.1405+5976A>C | DLG3 | ENSG00000082458.12 | transcript | ENST00000374360.8 | protein_coding | 9/18 | chrX | 70460292 | ||||||
| chrX:70460300
|
A | AC | 27 | a0001c0001t0001g0025a0001c0001t0001g0059a0001c0001t0001g0133others(24): Show | 27 | HG00642.hp1 HG01106.hp1 HG01346.hp1 others(24): Show |
intron_variant | MODIFIER | c.1405+5984_1405+598 others(5): Show |
DLG3 | ENSG00000082458.12 | transcript | ENST00000374360.8 | protein_coding | 9/18 | chrX | 70460300 | ||||||
| chrX:70460300
|
A | C | 122 | a0001c0001t0001g0015a0001c0001t0001g0016a0001c0001t0001g0017others(119): Show | 130 | HG00099.hp1 HG00621.hp1 HG00733.hp1 others(127): Show |
intron_variant | MODIFIER | c.1405+5984A>C | DLG3 | ENSG00000082458.12 | transcript | ENST00000374360.8 | protein_coding | 9/18 | chrX | 70460300 | ||||||
| chrX:70460397
|
TC | T | 1 | a0001c0001t0001g0152 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.1405+6084delC | DLG3 | ENSG00000082458.12 | transcript | ENST00000374360.8 | protein_coding | 9/18 | INFO_REALIGN_3_PRIME | chrX | 70460397 | |||||
| chrX:70460461
|
A | T | 2 | a0001c0001t0024g0052a0001c0001t0027g0051 | 2 | HG01081.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.1405+6145A>T | DLG3 | ENSG00000082458.12 | transcript | ENST00000374360.8 | protein_coding | 9/18 | chrX | 70460461 | ||||||
| chrX:70460461
|
AC | A | 1 | a0001c0001t0001g0152 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.1405+6149delC | DLG3 | ENSG00000082458.12 | transcript | ENST00000374360.8 | protein_coding | 9/18 | INFO_REALIGN_3_PRIME | chrX | 70460461 | |||||
| chrX:70460551
|
A | T | 13 | a0001c0001t0001g0023a0001c0001t0001g0024a0001c0001t0001g0145others(10): Show | 13 | HG00738.hp1 HG01261.hp1 HG01361.hp1 others(10): Show |
intron_variant | MODIFIER | c.1405+6235A>T | DLG3 | ENSG00000082458.12 | transcript | ENST00000374360.8 | protein_coding | 9/18 | chrX | 70460551 | ||||||
| chrX:70460562
|
A | T | 1 | a0001c0001t0002g0060 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.1405+6246A>T | DLG3 | ENSG00000082458.12 | transcript | ENST00000374360.8 | protein_coding | 9/18 | chrX | 70460562 | ||||||
| chrX:70460607
|
GACCTT | G | 1 | a0001c0001t0001g0026 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1405+6294_1405+629 others(9): Show |
DLG3 | ENSG00000082458.12 | transcript | ENST00000374360.8 | protein_coding | 9/18 | INFO_REALIGN_3_PRIME | chrX | 70460607 | |||||
| chrX:70460715
|
C | T | 1 | a0001c0001t0001g0243 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.1405+6399C>T | DLG3 | ENSG00000082458.12 | transcript | ENST00000374360.8 | protein_coding | 9/18 | chrX | 70460715 | ||||||
| chrX:70460728
|
AC | A | 1 | a0001c0001t0001g0152 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.1405+6415delC | DLG3 | ENSG00000082458.12 | transcript | ENST00000374360.8 | protein_coding | 9/18 | INFO_REALIGN_3_PRIME | chrX | 70460728 | |||||
| chrX:70460991
|
T | TC | 1 | a0001c0001t0001g0169 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.1405+6676dupC | DLG3 | ENSG00000082458.12 | transcript | ENST00000374360.8 | protein_coding | 9/18 | INFO_REALIGN_3_PRIME | chrX | 70460991 | |||||
| chrX:70461194
|
G | GT | 1 | a0001c0001t0001g0152 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.1405+6880dupT | DLG3 | ENSG00000082458.12 | transcript | ENST00000374360.8 | protein_coding | 9/18 | INFO_REALIGN_3_PRIME | chrX | 70461194 | |||||
| chrX:70461212
|
C | A | 1 | a0001c0001t0001g0152 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.1405+6896C>A | DLG3 | ENSG00000082458.12 | transcript | ENST00000374360.8 | protein_coding | 9/18 | chrX | 70461212 | ||||||
| chrX:70461213
|
A | T | 1 | a0001c0001t0001g0152 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.1405+6897A>T | DLG3 | ENSG00000082458.12 | transcript | ENST00000374360.8 | protein_coding | 9/18 | chrX | 70461213 | ||||||
| chrX:70461214
|
T | C | 1 | a0001c0001t0001g0152 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.1405+6898T>C | DLG3 | ENSG00000082458.12 | transcript | ENST00000374360.8 | protein_coding | 9/18 | chrX | 70461214 | ||||||
| chrX:70461371
|
TC | T | 1 | a0001c0001t0001g0152 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.1405+7059delC | DLG3 | ENSG00000082458.12 | transcript | ENST00000374360.8 | protein_coding | 9/18 | INFO_REALIGN_3_PRIME | chrX | 70461371 | |||||
| chrX:70461447
|
A | T | 1 | a0001c0001t0001g0048 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.1405+7131A>T | DLG3 | ENSG00000082458.12 | transcript | ENST00000374360.8 | protein_coding | 9/18 | chrX | 70461447 | ||||||
| chrX:70461472
|
TA | T | 1 | a0001c0001t0001g0169 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.1405+7158delA | DLG3 | ENSG00000082458.12 | transcript | ENST00000374360.8 | protein_coding | 9/18 | INFO_REALIGN_3_PRIME | chrX | 70461472 | |||||
| chrX:70461499
|
CG | C | 67 | a0001c0001t0001g0015a0001c0001t0001g0016a0001c0001t0001g0017others(64): Show | 74 | HG00733.hp1 HG00735.hp1 HG01070.hp2 others(71): Show |
intron_variant | MODIFIER | c.1405+7189delG | DLG3 | ENSG00000082458.12 | transcript | ENST00000374360.8 | protein_coding | 9/18 | INFO_REALIGN_3_PRIME | chrX | 70461499 | |||||
| chrX:70461567
|
G | GC | 7 | a0001c0001t0001g0152a0001c0001t0001g0190a0001c0001t0002g0247others(4): Show | 7 | HG02145.hp1 HG03831.hp2 HG03927.hp1 others(4): Show |
intron_variant | MODIFIER | c.1405+7258dupC | DLG3 | ENSG00000082458.12 | transcript | ENST00000374360.8 | protein_coding | 9/18 | INFO_REALIGN_3_PRIME | chrX | 70461567 | |||||
| chrX:70461574
|
C | CT | 2 | a0001c0001t0001g0189a0001c0001t0003g0168 | 2 | NA18967.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.1405+7272dupT | DLG3 | ENSG00000082458.12 | transcript | ENST00000374360.8 | protein_coding | 9/18 | INFO_REALIGN_3_PRIME | chrX | 70461574 | |||||
| chrX:70461574
|
CT | C | 16 | a0001c0001t0001g0026a0001c0001t0001g0029a0001c0001t0001g0038others(13): Show | 17 | HG00099.hp1 HG00642.hp1 HG00733.hp2 others(14): Show |
intron_variant | MODIFIER | c.1405+7272delT | DLG3 | ENSG00000082458.12 | transcript | ENST00000374360.8 | protein_coding | 9/18 | INFO_REALIGN_3_PRIME | chrX | 70461574 | |||||
| chrX:70461575
|
T | C | 22 | a0001c0001t0001g0044a0001c0001t0001g0045a0001c0001t0001g0046others(19): Show | 22 | HG01081.hp2 HG01255.hp1 HG02280.hp2 others(19): Show |
intron_variant | MODIFIER | c.1405+7259T>C | DLG3 | ENSG00000082458.12 | transcript | ENST00000374360.8 | protein_coding | 9/18 | chrX | 70461575 | ||||||
| chrX:70461576
|
T | C | 1 | a0001c0001t0020g0218 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.1405+7260T>C | DLG3 | ENSG00000082458.12 | transcript | ENST00000374360.8 | protein_coding | 9/18 | chrX | 70461576 | ||||||
| chrX:70461934
|
T | A | 6 | a0001c0002t0005g0039a0001c0002t0005g0040a0001c0002t0005g0041others(3): Show | 6 | HG01167.hp1 HG01169.hp1 HG02486.hp1 others(3): Show |
intron_variant | MODIFIER | c.1405+7618T>A | DLG3 | ENSG00000082458.12 | transcript | ENST00000374360.8 | protein_coding | 9/18 | chrX | 70461934 | ||||||
| chrX:70461941
|
AT | A | 1 | a0001c0001t0001g0152 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.1405+7630delT | DLG3 | ENSG00000082458.12 | transcript | ENST00000374360.8 | protein_coding | 9/18 | INFO_REALIGN_3_PRIME | chrX | 70461941 | |||||
| chrX:70462026
|
G | A | 23 | a0001c0001t0001g0044a0001c0001t0001g0045a0001c0001t0001g0046others(20): Show | 23 | HG01081.hp2 HG01255.hp1 HG02280.hp2 others(20): Show |
intron_variant | MODIFIER | c.1405+7710G>A | DLG3 | ENSG00000082458.12 | transcript | ENST00000374360.8 | protein_coding | 9/18 | chrX | 70462026 | ||||||
| chrX:70462040
|
T | TC | 20 | a0001c0001t0001g0022a0001c0001t0001g0140a0001c0001t0001g0167others(17): Show | 20 | HG00741.hp2 HG01169.hp1 HG01175.hp1 others(17): Show |
intron_variant | MODIFIER | c.1405+7733dupC | DLG3 | ENSG00000082458.12 | transcript | ENST00000374360.8 | protein_coding | 9/18 | INFO_REALIGN_3_PRIME | chrX | 70462040 | |||||
| chrX:70462040
|
T | TCC | 23 | a0001c0001t0001g0019a0001c0001t0001g0058a0001c0001t0001g0059others(20): Show | 24 | HG00621.hp1 HG01167.hp1 HG01261.hp1 others(21): Show |
intron_variant | MODIFIER | c.1405+7732_1405+773 others(6): Show |
DLG3 | ENSG00000082458.12 | transcript | ENST00000374360.8 | protein_coding | 9/18 | INFO_REALIGN_3_PRIME | chrX | 70462040 | |||||
| chrX:70462040
|
T | TCCC | 14 | a0001c0001t0001g0023a0001c0001t0001g0024a0001c0001t0001g0147others(11): Show | 14 | HG00738.hp1 HG02523.hp1 HG03831.hp2 others(11): Show |
intron_variant | MODIFIER | c.1405+7731_1405+773 others(7): Show |
DLG3 | ENSG00000082458.12 | transcript | ENST00000374360.8 | protein_coding | 9/18 | INFO_REALIGN_3_PRIME | chrX | 70462040 | |||||
| chrX:70462040
|
T | TCCCC | 5 | a0001c0001t0001g0188a0001c0001t0001g0190a0001c0001t0001g0198others(2): Show | 5 | NA18940.hp1 NA18946.hp1 NA18972.hp1 others(2): Show |
intron_variant | MODIFIER | c.1405+7730_1405+773 others(8): Show |
DLG3 | ENSG00000082458.12 | transcript | ENST00000374360.8 | protein_coding | 9/18 | INFO_REALIGN_3_PRIME | chrX | 70462040 | |||||
| chrX:70462040
|
T | TCCCCC | 1 | a0001c0001t0001g0201 | 1 | NA18991.hp2 | intron_variant | MODIFIER | c.1405+7729_1405+773 others(9): Show |
DLG3 | ENSG00000082458.12 | transcript | ENST00000374360.8 | protein_coding | 9/18 | INFO_REALIGN_3_PRIME | chrX | 70462040 | |||||
| chrX:70462046
|
C | CCCG | 1 | a0001c0001t0001g0189 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.1405+7732_1405+773 others(7): Show |
DLG3 | ENSG00000082458.12 | transcript | ENST00000374360.8 | protein_coding | 9/18 | INFO_REALIGN_3_PRIME | chrX | 70462046 | |||||
| chrX:70462046
|
C | T | 7 | a0001c0001t0004g0119a0001c0001t0004g0181a0001c0001t0004g0221others(4): Show | 7 | HG02055.hp1 HG02257.hp2 HG02922.hp1 others(4): Show |
intron_variant | MODIFIER | c.1405+7730C>T | DLG3 | ENSG00000082458.12 | transcript | ENST00000374360.8 | protein_coding | 9/18 | chrX | 70462046 | ||||||
| chrX:70462053
|
G | GC | 2 | a0001c0001t0001g0046a0001c0001t0001g0216 | 2 | HG01243.hp1 HG02615.hp2 |
intron_variant | MODIFIER | c.1405+7744dupC | DLG3 | ENSG00000082458.12 | transcript | ENST00000374360.8 | protein_coding | 9/18 | INFO_REALIGN_3_PRIME | chrX | 70462053 | |||||
| chrX:70462243
|
C | CT | 16 | a0001c0001t0002g0027a0001c0001t0002g0064a0001c0001t0002g0096others(13): Show | 16 | HG00741.hp2 HG02056.hp1 HG02071.hp1 others(13): Show |
intron_variant | MODIFIER | c.1405+7951dupT | DLG3 | ENSG00000082458.12 | transcript | ENST00000374360.8 | protein_coding | 9/18 | INFO_REALIGN_3_PRIME | chrX | 70462243 | |||||
| chrX:70462243
|
C | CTT | 1 | a0001c0001t0011g0043 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.1405+7950_1405+795 others(6): Show |
DLG3 | ENSG00000082458.12 | transcript | ENST00000374360.8 | protein_coding | 9/18 | INFO_REALIGN_3_PRIME | chrX | 70462243 | |||||
| chrX:70462243
|
CT | C | 116 | a0001c0001t0001g0015a0001c0001t0001g0016a0001c0001t0001g0017others(113): Show | 124 | HG00621.hp1 HG00733.hp1 HG00735.hp1 others(121): Show |
intron_variant | MODIFIER | c.1405+7951delT | DLG3 | ENSG00000082458.12 | transcript | ENST00000374360.8 | protein_coding | 9/18 | INFO_REALIGN_3_PRIME | chrX | 70462243 | |||||
| chrX:70462243
|
CTT | C | 19 | a0001c0001t0001g0029a0001c0001t0001g0038a0001c0001t0001g0202others(16): Show | 20 | HG00099.hp1 HG00642.hp1 HG00733.hp2 others(17): Show |
intron_variant | MODIFIER | c.1405+7950_1405+795 others(6): Show |
DLG3 | ENSG00000082458.12 | transcript | ENST00000374360.8 | protein_coding | 9/18 | INFO_REALIGN_3_PRIME | chrX | 70462243 | |||||
| chrX:70462247
|
T | C | 1 | a0001c0001t0003g0168 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1405+7931T>C | DLG3 | ENSG00000082458.12 | transcript | ENST00000374360.8 | protein_coding | 9/18 | chrX | 70462247 | ||||||
| chrX:70462248
|
T | C | 26 | a0001c0001t0001g0015a0001c0001t0001g0016a0001c0001t0001g0025others(23): Show | 30 | HG01109.hp1 HG01123.hp1 HG01257.hp1 others(27): Show |
intron_variant | MODIFIER | c.1405+7932T>C | DLG3 | ENSG00000082458.12 | transcript | ENST00000374360.8 | protein_coding | 9/18 | chrX | 70462248 | ||||||
| chrX:70462249
|
T | C | 1 | a0004c0005t0001g0172 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.1405+7933T>C | DLG3 | ENSG00000082458.12 | transcript | ENST00000374360.8 | protein_coding | 9/18 | chrX | 70462249 | ||||||
| chrX:70462281
|
A | G | 1 | a0001c0001t0020g0218 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.1405+7965A>G | DLG3 | ENSG00000082458.12 | transcript | ENST00000374360.8 | protein_coding | 9/18 | chrX | 70462281 | ||||||
| chrX:70462391
|
A | C | 4 | a0001c0002t0005g0039a0001c0002t0005g0040a0001c0002t0005g0041others(1): Show | 4 | HG02486.hp1 HG02895.hp1 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.1405+8075A>C | DLG3 | ENSG00000082458.12 | transcript | ENST00000374360.8 | protein_coding | 9/18 | chrX | 70462391 | ||||||
| chrX:70462501
|
CG | C | 1 | a0001c0001t0001g0152 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.1405+8187delG | DLG3 | ENSG00000082458.12 | transcript | ENST00000374360.8 | protein_coding | 9/18 | INFO_REALIGN_3_PRIME | chrX | 70462501 | |||||
| chrX:70462540
|
G | A | 1 | a0001c0001t0002g0098 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.1405+8224G>A | DLG3 | ENSG00000082458.12 | transcript | ENST00000374360.8 | protein_coding | 9/18 | chrX | 70462540 | ||||||
| chrX:70462553
|
C | T | 1 | a0001c0001t0001g0026 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1405+8237C>T | DLG3 | ENSG00000082458.12 | transcript | ENST00000374360.8 | protein_coding | 9/18 | chrX | 70462553 | ||||||
| chrX:70462685
|
TGAACATT others(1): Show |
T | 1 | a0001c0001t0002g0112 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.1405+8370_1405+837 others(12): Show |
DLG3 | ENSG00000082458.12 | transcript | ENST00000374360.8 | protein_coding | 9/18 | chrX | 70462685 | ||||||
| chrX:70462748
|
AG | A | 1 | a0001c0001t0001g0169 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.1405+8434delG | DLG3 | ENSG00000082458.12 | transcript | ENST00000374360.8 | protein_coding | 9/18 | INFO_REALIGN_3_PRIME | chrX | 70462748 | |||||
| chrX:70462817
|
A | T | 153 | a0001c0001t0001g0015a0001c0001t0001g0016a0001c0001t0001g0017others(150): Show | 162 | HG00099.hp1 HG00621.hp1 HG00642.hp1 others(159): Show |
intron_variant | MODIFIER | c.1405+8501A>T | DLG3 | ENSG00000082458.12 | transcript | ENST00000374360.8 | protein_coding | 9/18 | chrX | 70462817 | ||||||
| chrX:70462855
|
T | G | 1 | a0001c0001t0022g0227 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.1405+8539T>G | DLG3 | ENSG00000082458.12 | transcript | ENST00000374360.8 | protein_coding | 9/18 | chrX | 70462855 | ||||||
| chrX:70462899
|
GC | G | 1 | a0001c0001t0001g0152 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.1405+8588delC | DLG3 | ENSG00000082458.12 | transcript | ENST00000374360.8 | protein_coding | 9/18 | INFO_REALIGN_3_PRIME | chrX | 70462899 | |||||
| chrX:70462924
|
T | C | 1 | a0001c0001t0001g0053 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.1405+8608T>C | DLG3 | ENSG00000082458.12 | transcript | ENST00000374360.8 | protein_coding | 9/18 | chrX | 70462924 | ||||||
| chrX:70463036
|
GGTT | G | 1 | a0008c0010t0031g0245 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.1405+8721_1405+872 others(7): Show |
DLG3 | ENSG00000082458.12 | transcript | ENST00000374360.8 | protein_coding | 9/18 | chrX | 70463036 | ||||||
| chrX:70463081
|
G | GT | 1 | a0001c0001t0001g0169 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.1405+8770dupT | DLG3 | ENSG00000082458.12 | transcript | ENST00000374360.8 | protein_coding | 9/18 | INFO_REALIGN_3_PRIME | chrX | 70463081 | |||||
| chrX:70463157
|
A | AT | 1 | a0008c0010t0031g0245 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.1405+8848dupT | DLG3 | ENSG00000082458.12 | transcript | ENST00000374360.8 | protein_coding | 9/18 | INFO_REALIGN_3_PRIME | chrX | 70463157 | |||||
| chrX:70463157
|
AT | A | 1 | a0001c0001t0002g0130 | 1 | NA19055.hp1 | intron_variant | MODIFIER | c.1405+8848delT | DLG3 | ENSG00000082458.12 | transcript | ENST00000374360.8 | protein_coding | 9/18 | INFO_REALIGN_3_PRIME | chrX | 70463157 | |||||
| chrX:70463399
|
G | A | 1 | a0001c0001t0001g0026 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1405+9083G>A | DLG3 | ENSG00000082458.12 | transcript | ENST00000374360.8 | protein_coding | 9/18 | chrX | 70463399 | ||||||
| chrX:70463442
|
A | G | 38 | a0001c0001t0001g0019a0001c0001t0001g0023a0001c0001t0001g0024others(35): Show | 38 | HG00621.hp1 HG01261.hp1 HG01361.hp1 others(35): Show |
intron_variant | MODIFIER | c.1405+9126A>G | DLG3 | ENSG00000082458.12 | transcript | ENST00000374360.8 | protein_coding | 9/18 | chrX | 70463442 | ||||||
| chrX:70463449
|
A | AG | 1 | a0008c0010t0031g0245 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.1405+9134dupG | DLG3 | ENSG00000082458.12 | transcript | ENST00000374360.8 | protein_coding | 9/18 | INFO_REALIGN_3_PRIME | chrX | 70463449 | |||||
| chrX:70463538
|
A | C | 1 | a0001c0001t0002g0116 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.1405+9222A>C | DLG3 | ENSG00000082458.12 | transcript | ENST00000374360.8 | protein_coding | 9/18 | chrX | 70463538 | ||||||
| chrX:70463668
|
C | G | 16 | a0001c0001t0001g0026a0001c0001t0001g0029a0001c0001t0001g0038others(13): Show | 17 | HG00099.hp1 HG00642.hp1 HG00733.hp2 others(14): Show |
intron_variant | MODIFIER | c.1405+9352C>G | DLG3 | ENSG00000082458.12 | transcript | ENST00000374360.8 | protein_coding | 9/18 | chrX | 70463668 | ||||||
| chrX:70463809
|
A | C | 1 | a0001c0001t0002g0093 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.1405+9493A>C | DLG3 | ENSG00000082458.12 | transcript | ENST00000374360.8 | protein_coding | 9/18 | chrX | 70463809 | ||||||
| chrX:70464190
|
T | TTTTCC | 10 | a0001c0001t0002g0074a0001c0001t0002g0080a0001c0001t0002g0081others(7): Show | 10 | HG01993.hp1 HG02129.hp1 HG02132.hp1 others(7): Show |
intron_variant | MODIFIER | c.1405+9909_1405+991 others(9): Show |
DLG3 | ENSG00000082458.12 | transcript | ENST00000374360.8 | protein_coding | 9/18 | INFO_REALIGN_3_PRIME | chrX | 70464190 | |||||
| chrX:70464190
|
T | TTTTCCTT others(3): Show |
1 | a0005c0008t0002g0129 | 1 | NA18988.hp1 | intron_variant | MODIFIER | c.1405+9904_1405+991 others(14): Show |
DLG3 | ENSG00000082458.12 | transcript | ENST00000374360.8 | protein_coding | 9/18 | INFO_REALIGN_3_PRIME | chrX | 70464190 | |||||
| chrX:70464190
|
TTTTCC | T | 1 | a0001c0001t0002g0092 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.1405+9909_1405+991 others(9): Show |
DLG3 | ENSG00000082458.12 | transcript | ENST00000374360.8 | protein_coding | 9/18 | INFO_REALIGN_3_PRIME | chrX | 70464190 | |||||
| chrX:70464190
|
TTTTCCTT others(3): Show |
T | 147 | a0001c0001t0001g0015a0001c0001t0001g0016a0001c0001t0001g0017others(144): Show | 155 | HG00099.hp1 HG00621.hp1 HG00642.hp1 others(152): Show |
intron_variant | MODIFIER | c.1405+9904_1405+991 others(14): Show |
DLG3 | ENSG00000082458.12 | transcript | ENST00000374360.8 | protein_coding | 9/18 | INFO_REALIGN_3_PRIME | chrX | 70464190 | |||||
| chrX:70464190
|
TTTTCCTT others(8): Show |
T | 2 | a0001c0001t0001g0029a0001c0001t0001g0204 | 2 | HG02280.hp1 HG02630.hp2 |
intron_variant | MODIFIER | c.1405+9899_1405+991 others(19): Show |
DLG3 | ENSG00000082458.12 | transcript | ENST00000374360.8 | protein_coding | 9/18 | INFO_REALIGN_3_PRIME | chrX | 70464190 | |||||
| chrX:70464444
|
A | G | 1 | a0001c0001t0001g0226 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1405+10128A>G | DLG3 | ENSG00000082458.12 | transcript | ENST00000374360.8 | protein_coding | 9/18 | chrX | 70464444 | ||||||
| chrX:70464629
|
A | T | 2 | a0001c0001t0006g0111a0001c0001t0018g0070 | 2 | NA18966.hp1 NA19063.hp1 |
intron_variant | MODIFIER | c.1405+10313A>T | DLG3 | ENSG00000082458.12 | transcript | ENST00000374360.8 | protein_coding | 9/18 | chrX | 70464629 | ||||||
| chrX:70464759
|
C | T | 1 | a0001c0001t0003g0028 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.1405+10443C>T | DLG3 | ENSG00000082458.12 | transcript | ENST00000374360.8 | protein_coding | 9/18 | chrX | 70464759 | ||||||
| chrX:70465032
|
G | A | 1 | a0001c0001t0002g0100 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.1405+10716G>A | DLG3 | ENSG00000082458.12 | transcript | ENST00000374360.8 | protein_coding | 9/18 | chrX | 70465032 | ||||||
| chrX:70465157
|
C | T | 1 | a0001c0001t0001g0230 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.1405+10841C>T | DLG3 | ENSG00000082458.12 | transcript | ENST00000374360.8 | protein_coding | 9/18 | chrX | 70465157 | ||||||
| chrX:70465573
|
T | G | 3 | a0001c0001t0001g0228a0001c0001t0001g0229a0001c0001t0001g0230 | 3 | HG02896.hp2 HG02897.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.1405+11257T>G | DLG3 | ENSG00000082458.12 | transcript | ENST00000374360.8 | protein_coding | 9/18 | chrX | 70465573 | ||||||
| chrX:70465674
|
T | A | 1 | a0001c0001t0020g0218 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.1405+11358T>A | DLG3 | ENSG00000082458.12 | transcript | ENST00000374360.8 | protein_coding | 9/18 | chrX | 70465674 | ||||||
| chrX:70465780
|
AT | A | 1 | a0001c0001t0002g0082 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.1405+11468delT | DLG3 | ENSG00000082458.12 | transcript | ENST00000374360.8 | protein_coding | 9/18 | INFO_REALIGN_3_PRIME | chrX | 70465780 | |||||
| chrX:70465800
|
AT | A | 1 | a0006c0006t0015g0057 | 1 | NA18949.hp1 | intron_variant | MODIFIER | c.1405+11490delT | DLG3 | ENSG00000082458.12 | transcript | ENST00000374360.8 | protein_coding | 9/18 | INFO_REALIGN_3_PRIME | chrX | 70465800 | |||||
| chrX:70465905
|
A | G | 14 | a0001c0001t0001g0029a0001c0001t0001g0038a0001c0001t0001g0204others(11): Show | 15 | HG00099.hp1 HG00642.hp1 HG00733.hp2 others(12): Show |
intron_variant | MODIFIER | c.1405+11589A>G | DLG3 | ENSG00000082458.12 | transcript | ENST00000374360.8 | protein_coding | 9/18 | chrX | 70465905 | ||||||
| chrX:70465951
|
G | A | 5 | a0001c0001t0003g0008a0001c0001t0003g0028a0001c0001t0003g0030others(2): Show | 6 | HG00099.hp1 HG00642.hp1 HG01070.hp1 others(3): Show |
intron_variant | MODIFIER | c.1405+11635G>A | DLG3 | ENSG00000082458.12 | transcript | ENST00000374360.8 | protein_coding | 9/18 | chrX | 70465951 | ||||||
| chrX:70465978
|
C | T | 67 | a0001c0001t0001g0015a0001c0001t0001g0016a0001c0001t0001g0017others(64): Show | 74 | HG00733.hp1 HG00735.hp1 HG01070.hp2 others(71): Show |
intron_variant | MODIFIER | c.1405+11662C>T | DLG3 | ENSG00000082458.12 | transcript | ENST00000374360.8 | protein_coding | 9/18 | chrX | 70465978 | ||||||
| chrX:70466163
|
G | A | 10 | a0001c0001t0003g0008a0001c0001t0003g0028a0001c0001t0003g0030others(7): Show | 11 | HG00099.hp1 HG00642.hp1 HG00733.hp2 others(8): Show |
intron_variant | MODIFIER | c.1405+11847G>A | DLG3 | ENSG00000082458.12 | transcript | ENST00000374360.8 | protein_coding | 9/18 | chrX | 70466163 | ||||||
| chrX:70466178
|
G | T | 28 | a0001c0001t0001g0015a0001c0001t0001g0016a0001c0001t0001g0025others(25): Show | 32 | HG01109.hp1 HG01123.hp1 HG01257.hp1 others(29): Show |
intron_variant | MODIFIER | c.1405+11862G>T | DLG3 | ENSG00000082458.12 | transcript | ENST00000374360.8 | protein_coding | 9/18 | chrX | 70466178 | ||||||
| chrX:70466219
|
C | G | 1 | a0001c0001t0001g0152 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.1405+11903C>G | DLG3 | ENSG00000082458.12 | transcript | ENST00000374360.8 | protein_coding | 9/18 | chrX | 70466219 | ||||||
| chrX:70466247
|
T | TG | 1 | a0001c0001t0002g0101 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.1405+11931_1405+11 others(7): Show |
DLG3 | ENSG00000082458.12 | transcript | ENST00000374360.8 | protein_coding | 9/18 | chrX | 70466247 | ||||||
| chrX:70466247
|
T | TTG | 35 | a0001c0001t0001g0023a0001c0001t0001g0174a0001c0001t0001g0194others(32): Show | 40 | HG00438.hp1 HG00438.hp2 HG00621.hp1 others(37): Show |
intron_variant | MODIFIER | c.1405+11978_1405+11 others(8): Show |
DLG3 | ENSG00000082458.12 | transcript | ENST00000374360.8 | protein_coding | 9/18 | INFO_REALIGN_3_PRIME | chrX | 70466247 | |||||
| chrX:70466247
|
T | TTGTA | 1 | a0001c0001t0002g0102 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.1405+11934_1405+11 others(10): Show |
DLG3 | ENSG00000082458.12 | transcript | ENST00000374360.8 | protein_coding | 9/18 | INFO_REALIGN_3_PRIME | chrX | 70466247 | |||||
| chrX:70466247
|
T | TTGTG | 16 | a0001c0001t0001g0048a0001c0001t0001g0049a0001c0001t0001g0230others(13): Show | 16 | HG00099.hp2 HG01346.hp2 HG01516.hp1 others(13): Show |
intron_variant | MODIFIER | c.1405+11976_1405+11 others(10): Show |
DLG3 | ENSG00000082458.12 | transcript | ENST00000374360.8 | protein_coding | 9/18 | INFO_REALIGN_3_PRIME | chrX | 70466247 | |||||
| chrX:70466247
|
T | TTGTGTG | 2 | a0001c0001t0001g0235a0001c0001t0001g0236 | 2 | HG03453.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.1405+11974_1405+11 others(12): Show |
DLG3 | ENSG00000082458.12 | transcript | ENST00000374360.8 | protein_coding | 9/18 | INFO_REALIGN_3_PRIME | chrX | 70466247 | |||||
| chrX:70466247
|
T | TTGTGTGT others(1): Show |
1 | a0001c0001t0001g0137 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.1405+11972_1405+11 others(14): Show |
DLG3 | ENSG00000082458.12 | transcript | ENST00000374360.8 | protein_coding | 9/18 | INFO_REALIGN_3_PRIME | chrX | 70466247 | |||||
| chrX:70466247
|
TTG | T | 35 | a0001c0001t0001g0019a0001c0001t0001g0024a0001c0001t0001g0058others(32): Show | 36 | HG00738.hp1 HG01175.hp2 HG01261.hp1 others(33): Show |
intron_variant | MODIFIER | c.1405+11978_1405+11 others(8): Show |
DLG3 | ENSG00000082458.12 | transcript | ENST00000374360.8 | protein_coding | 9/18 | INFO_REALIGN_3_PRIME | chrX | 70466247 | |||||
| chrX:70466247
|
TTGTG | T | 6 | a0001c0001t0001g0155a0001c0001t0001g0191a0001c0001t0003g0030others(3): Show | 6 | HG00642.hp1 HG00733.hp2 HG02717.hp1 others(3): Show |
intron_variant | MODIFIER | c.1405+11976_1405+11 others(10): Show |
DLG3 | ENSG00000082458.12 | transcript | ENST00000374360.8 | protein_coding | 9/18 | INFO_REALIGN_3_PRIME | chrX | 70466247 | |||||
| chrX:70466247
|
TTGTGTG | T | 22 | a0001c0001t0001g0021a0001c0001t0001g0022a0001c0001t0001g0026others(19): Show | 23 | HG00099.hp1 HG00735.hp1 HG00741.hp1 others(20): Show |
intron_variant | MODIFIER | c.1405+11974_1405+11 others(12): Show |
DLG3 | ENSG00000082458.12 | transcript | ENST00000374360.8 | protein_coding | 9/18 | INFO_REALIGN_3_PRIME | chrX | 70466247 | |||||
| chrX:70466247
|
TTGTGTGT others(1): Show |
T | 52 | a0001c0001t0001g0015a0001c0001t0001g0016a0001c0001t0001g0017others(49): Show | 59 | HG00733.hp1 HG01070.hp2 HG01106.hp1 others(56): Show |
intron_variant | MODIFIER | c.1405+11972_1405+11 others(14): Show |
DLG3 | ENSG00000082458.12 | transcript | ENST00000374360.8 | protein_coding | 9/18 | INFO_REALIGN_3_PRIME | chrX | 70466247 | |||||
| chrX:70466247
|
TTGTGTGT others(3): Show |
T | 2 | a0001c0001t0001g0029a0001c0001t0001g0205 | 2 | HG02280.hp1 HG02615.hp1 |
intron_variant | MODIFIER | c.1405+11970_1405+11 others(16): Show |
DLG3 | ENSG00000082458.12 | transcript | ENST00000374360.8 | protein_coding | 9/18 | INFO_REALIGN_3_PRIME | chrX | 70466247 | |||||
| chrX:70466247
|
TTGTGTGT others(13): Show |
T | 1 | a0001c0001t0001g0226 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1405+11960_1405+11 others(26): Show |
DLG3 | ENSG00000082458.12 | transcript | ENST00000374360.8 | protein_coding | 9/18 | INFO_REALIGN_3_PRIME | chrX | 70466247 | |||||
| chrX:70466409
|
G | A | 2 | a0001c0001t0001g0026a0001c0001t0022g0227 | 2 | HG02886.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.1405+12093G>A | DLG3 | ENSG00000082458.12 | transcript | ENST00000374360.8 | protein_coding | 9/18 | chrX | 70466409 | ||||||
| chrX:70466441
|
C | CT | 1 | a0001c0001t0022g0227 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.1405+12140dupT | DLG3 | ENSG00000082458.12 | transcript | ENST00000374360.8 | protein_coding | 9/18 | INFO_REALIGN_3_PRIME | chrX | 70466441 | |||||
| chrX:70466441
|
CT | C | 37 | a0001c0001t0001g0019a0001c0001t0001g0023a0001c0001t0001g0024others(34): Show | 37 | HG00621.hp1 HG00738.hp1 HG01261.hp1 others(34): Show |
intron_variant | MODIFIER | c.1405+12140delT | DLG3 | ENSG00000082458.12 | transcript | ENST00000374360.8 | protein_coding | 9/18 | INFO_REALIGN_3_PRIME | chrX | 70466441 | |||||
| chrX:70466441
|
CTT | C | 1 | a0001c0001t0001g0193 | 1 | NA18957.hp1 | intron_variant | MODIFIER | c.1405+12139_1405+12 others(8): Show |
DLG3 | ENSG00000082458.12 | transcript | ENST00000374360.8 | protein_coding | 9/18 | INFO_REALIGN_3_PRIME | chrX | 70466441 | |||||
| chrX:70466629
|
G | A | 67 | a0001c0001t0001g0015a0001c0001t0001g0016a0001c0001t0001g0017others(64): Show | 74 | HG00733.hp1 HG00735.hp1 HG01070.hp2 others(71): Show |
intron_variant | MODIFIER | c.1405+12313G>A | DLG3 | ENSG00000082458.12 | transcript | ENST00000374360.8 | protein_coding | 9/18 | chrX | 70466629 | ||||||
| chrX:70466877
|
C | T | 7 | a0001c0001t0001g0021a0001c0001t0001g0022a0001c0001t0001g0224others(4): Show | 7 | HG01884.hp1 HG02109.hp1 HG02145.hp1 others(4): Show |
intron_variant | MODIFIER | c.1406-12273C>T | DLG3 | ENSG00000082458.12 | transcript | ENST00000374360.8 | protein_coding | 9/18 | chrX | 70466877 | ||||||
| chrX:70466915
|
ATTTG | A | 1 | a0001c0001t0001g0240 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.1406-12232_1406-12 others(10): Show |
DLG3 | ENSG00000082458.12 | transcript | ENST00000374360.8 | protein_coding | 9/18 | INFO_REALIGN_3_PRIME | chrX | 70466915 | |||||
| chrX:70467069
|
A | G | 1 | a0001c0001t0001g0026 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1406-12081A>G | DLG3 | ENSG00000082458.12 | transcript | ENST00000374360.8 | protein_coding | 9/18 | chrX | 70467069 | ||||||
| chrX:70467254
|
G | T | 1 | a0001c0001t0006g0061 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.1406-11896G>T | DLG3 | ENSG00000082458.12 | transcript | ENST00000374360.8 | protein_coding | 9/18 | chrX | 70467254 | ||||||
| chrX:70467364
|
C | T | 2 | a0001c0001t0024g0052a0001c0001t0027g0051 | 2 | HG01081.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.1406-11786C>T | DLG3 | ENSG00000082458.12 | transcript | ENST00000374360.8 | protein_coding | 9/18 | chrX | 70467364 | ||||||
| chrX:70467817
|
G | A | 1 | a0007c0004t0002g0131 | 1 | NA18972.hp2 | intron_variant | MODIFIER | c.1406-11333G>A | DLG3 | ENSG00000082458.12 | transcript | ENST00000374360.8 | protein_coding | 9/18 | chrX | 70467817 | ||||||
| chrX:70467994
|
T | C | 1 | a0001c0001t0001g0194 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.1406-11156T>C | DLG3 | ENSG00000082458.12 | transcript | ENST00000374360.8 | protein_coding | 9/18 | chrX | 70467994 | ||||||
| chrX:70468032
|
C | T | 6 | a0001c0002t0005g0039a0001c0002t0005g0040a0001c0002t0005g0041others(3): Show | 6 | HG01167.hp1 HG01169.hp1 HG02486.hp1 others(3): Show |
intron_variant | MODIFIER | c.1406-11118C>T | DLG3 | ENSG00000082458.12 | transcript | ENST00000374360.8 | protein_coding | 9/18 | chrX | 70468032 | ||||||
| chrX:70468193
|
C | T | 22 | a0001c0001t0001g0044a0001c0001t0001g0045a0001c0001t0001g0046others(19): Show | 22 | HG01081.hp2 HG01255.hp1 HG02280.hp2 others(19): Show |
intron_variant | MODIFIER | c.1406-10957C>T | DLG3 | ENSG00000082458.12 | transcript | ENST00000374360.8 | protein_coding | 9/18 | chrX | 70468193 | ||||||
| chrX:70468290
|
A | G | 155 | a0001c0001t0001g0015a0001c0001t0001g0016a0001c0001t0001g0017others(152): Show | 164 | HG00099.hp1 HG00621.hp1 HG00642.hp1 others(161): Show |
intron_variant | MODIFIER | c.1406-10860A>G | DLG3 | ENSG00000082458.12 | transcript | ENST00000374360.8 | protein_coding | 9/18 | chrX | 70468290 | ||||||
| chrX:70468356
|
C | T | 1 | a0001c0001t0001g0029 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.1406-10794C>T | DLG3 | ENSG00000082458.12 | transcript | ENST00000374360.8 | protein_coding | 9/18 | chrX | 70468356 | ||||||
| chrX:70468525
|
A | G | 1 | a0001c0001t0020g0218 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.1406-10625A>G | DLG3 | ENSG00000082458.12 | transcript | ENST00000374360.8 | protein_coding | 9/18 | chrX | 70468525 | ||||||
| chrX:70468559
|
G | A | 1 | a0001c0001t0004g0232 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.1406-10591G>A | DLG3 | ENSG00000082458.12 | transcript | ENST00000374360.8 | protein_coding | 9/18 | chrX | 70468559 | ||||||
| chrX:70468723
|
A | G | 1 | a0001c0001t0022g0227 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.1406-10427A>G | DLG3 | ENSG00000082458.12 | transcript | ENST00000374360.8 | protein_coding | 9/18 | chrX | 70468723 | ||||||
| chrX:70468924
|
G | A | 13 | a0001c0001t0001g0029a0001c0001t0001g0038a0001c0001t0001g0204others(10): Show | 14 | HG00099.hp1 HG00642.hp1 HG00733.hp2 others(11): Show |
intron_variant | MODIFIER | c.1406-10226G>A | DLG3 | ENSG00000082458.12 | transcript | ENST00000374360.8 | protein_coding | 9/18 | chrX | 70468924 | ||||||
| chrX:70469007
|
T | C | 2 | a0001c0001t0001g0026a0001c0001t0022g0227 | 2 | HG02886.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.1406-10143T>C | DLG3 | ENSG00000082458.12 | transcript | ENST00000374360.8 | protein_coding | 9/18 | chrX | 70469007 | ||||||
| chrX:70469159
|
C | T | 67 | a0001c0001t0001g0015a0001c0001t0001g0016a0001c0001t0001g0017others(64): Show | 74 | HG00733.hp1 HG00735.hp1 HG01070.hp2 others(71): Show |
intron_variant | MODIFIER | c.1406-9991C>T | DLG3 | ENSG00000082458.12 | transcript | ENST00000374360.8 | protein_coding | 9/18 | chrX | 70469159 | ||||||
| chrX:70469180
|
C | T | 2 | a0001c0001t0002g0097a0001c0001t0002g0118 | 2 | NA18960.hp1 NA19082.hp1 |
intron_variant | MODIFIER | c.1406-9970C>T | DLG3 | ENSG00000082458.12 | transcript | ENST00000374360.8 | protein_coding | 9/18 | chrX | 70469180 | ||||||
| chrX:70469185
|
A | AT | 3 | a0001c0001t0001g0149a0001c0001t0001g0150a0001c0001t0001g0151 | 3 | NA19002.hp2 NA19011.hp1 NA19074.hp1 |
intron_variant | MODIFIER | c.1406-9957dupT | DLG3 | ENSG00000082458.12 | transcript | ENST00000374360.8 | protein_coding | 9/18 | INFO_REALIGN_3_PRIME | chrX | 70469185 | |||||
| chrX:70469315
|
A | G | 6 | a0001c0002t0005g0039a0001c0002t0005g0040a0001c0002t0005g0041others(3): Show | 6 | HG01167.hp1 HG01169.hp1 HG02486.hp1 others(3): Show |
intron_variant | MODIFIER | c.1406-9835A>G | DLG3 | ENSG00000082458.12 | transcript | ENST00000374360.8 | protein_coding | 9/18 | chrX | 70469315 | ||||||
| chrX:70469446
|
CT | C | 4 | a0001c0001t0001g0152a0001c0001t0001g0160a0001c0001t0001g0166others(1): Show | 4 | HG01074.hp1 NA18941.hp2 NA18942.hp2 others(1): Show |
intron_variant | MODIFIER | c.1406-9690delT | DLG3 | ENSG00000082458.12 | transcript | ENST00000374360.8 | protein_coding | 9/18 | INFO_REALIGN_3_PRIME | chrX | 70469446 | |||||
| chrX:70469452
|
T | C | 1 | a0001c0001t0002g0093 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.1406-9698T>C | DLG3 | ENSG00000082458.12 | transcript | ENST00000374360.8 | protein_coding | 9/18 | chrX | 70469452 | ||||||
| chrX:70469512
|
G | A | 1 | a0001c0001t0012g0006 | 3 | HG00733.hp1 NA20752.hp1 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.1406-9638G>A | DLG3 | ENSG00000082458.12 | transcript | ENST00000374360.8 | protein_coding | 9/18 | chrX | 70469512 | ||||||
| chrX:70469639
|
G | A | 1 | a0001c0001t0002g0027 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.1406-9511G>A | DLG3 | ENSG00000082458.12 | transcript | ENST00000374360.8 | protein_coding | 9/18 | chrX | 70469639 | ||||||
| chrX:70469792
|
C | A | 1 | a0001c0001t0010g0154 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.1406-9358C>A | DLG3 | ENSG00000082458.12 | transcript | ENST00000374360.8 | protein_coding | 9/18 | chrX | 70469792 | ||||||
| chrX:70469818
|
A | C | 115 | a0001c0001t0001g0015a0001c0001t0001g0016a0001c0001t0001g0017others(112): Show | 122 | HG00621.hp1 HG00733.hp1 HG00735.hp1 others(119): Show |
intron_variant | MODIFIER | c.1406-9332A>C | DLG3 | ENSG00000082458.12 | transcript | ENST00000374360.8 | protein_coding | 9/18 | chrX | 70469818 | ||||||
| chrX:70469911
|
A | C | 1 | a0001c0001t0001g0148 | 1 | NA18980.hp1 | intron_variant | MODIFIER | c.1406-9239A>C | DLG3 | ENSG00000082458.12 | transcript | ENST00000374360.8 | protein_coding | 9/18 | chrX | 70469911 | ||||||
| chrX:70470254
|
A | G | 1 | a0001c0001t0001g0204 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.1406-8896A>G | DLG3 | ENSG00000082458.12 | transcript | ENST00000374360.8 | protein_coding | 9/18 | chrX | 70470254 | ||||||
| chrX:70470333
|
C | T | 1 | a0001c0001t0011g0214 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.1406-8817C>T | DLG3 | ENSG00000082458.12 | transcript | ENST00000374360.8 | protein_coding | 9/18 | chrX | 70470333 | ||||||
| chrX:70470465
|
C | T | 2 | a0001c0001t0001g0134a0001c0001t0001g0219 | 2 | HG03491.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.1406-8685C>T | DLG3 | ENSG00000082458.12 | transcript | ENST00000374360.8 | protein_coding | 9/18 | chrX | 70470465 | ||||||
| chrX:70470523
|
AC | A | 1 | a0001c0001t0001g0161 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.1406-8624delC | DLG3 | ENSG00000082458.12 | transcript | ENST00000374360.8 | protein_coding | 9/18 | INFO_REALIGN_3_PRIME | chrX | 70470523 | |||||
| chrX:70470566
|
T | C | 2 | a0001c0001t0001g0206a0001c0001t0001g0237 | 2 | HG02109.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.1406-8584T>C | DLG3 | ENSG00000082458.12 | transcript | ENST00000374360.8 | protein_coding | 9/18 | chrX | 70470566 | ||||||
| chrX:70470609
|
G | A | 148 | a0001c0001t0001g0015a0001c0001t0001g0016a0001c0001t0001g0017others(145): Show | 156 | HG00099.hp1 HG00621.hp1 HG00642.hp1 others(153): Show |
intron_variant | MODIFIER | c.1406-8541G>A | DLG3 | ENSG00000082458.12 | transcript | ENST00000374360.8 | protein_coding | 9/18 | chrX | 70470609 | ||||||
| chrX:70470819
|
T | C | 1 | a0001c0001t0001g0046 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.1406-8331T>C | DLG3 | ENSG00000082458.12 | transcript | ENST00000374360.8 | protein_coding | 9/18 | chrX | 70470819 | ||||||
| chrX:70470850
|
G | GT | 1 | a0001c0001t0004g0181 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.1406-8299dupT | DLG3 | ENSG00000082458.12 | transcript | ENST00000374360.8 | protein_coding | 9/18 | INFO_REALIGN_3_PRIME | chrX | 70470850 | |||||
| chrX:70470864
|
C | A | 20 | a0001c0001t0001g0023a0001c0001t0001g0024a0001c0001t0001g0145others(17): Show | 20 | HG00738.hp1 HG01167.hp1 HG01169.hp1 others(17): Show |
intron_variant | MODIFIER | c.1406-8286C>A | DLG3 | ENSG00000082458.12 | transcript | ENST00000374360.8 | protein_coding | 9/18 | chrX | 70470864 | ||||||
| chrX:70470964
|
T | TC | 1 | a0001c0001t0001g0161 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.1406-8186_1406-818 others(5): Show |
DLG3 | ENSG00000082458.12 | transcript | ENST00000374360.8 | protein_coding | 9/18 | chrX | 70470964 | ||||||
| chrX:70470980
|
T | G | 2 | a0001c0001t0001g0142a0001c0001t0001g0182 | 2 | HG02647.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.1406-8170T>G | DLG3 | ENSG00000082458.12 | transcript | ENST00000374360.8 | protein_coding | 9/18 | chrX | 70470980 | ||||||
| chrX:70470996
|
G | A | 1 | a0001c0001t0021g0018 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.1406-8154G>A | DLG3 | ENSG00000082458.12 | transcript | ENST00000374360.8 | protein_coding | 9/18 | chrX | 70470996 | ||||||
| chrX:70471000
|
G | A | 2 | a0001c0001t0006g0143a0001c0001t0010g0186 | 2 | HG03831.hp2 HG04115.hp1 |
intron_variant | MODIFIER | c.1406-8150G>A | DLG3 | ENSG00000082458.12 | transcript | ENST00000374360.8 | protein_coding | 9/18 | chrX | 70471000 | ||||||
| chrX:70471023
|
C | CT | 2 | a0001c0001t0002g0081a0001c0001t0020g0218 | 2 | HG02683.hp2 HG02886.hp1 |
intron_variant | MODIFIER | c.1406-8116dupT | DLG3 | ENSG00000082458.12 | transcript | ENST00000374360.8 | protein_coding | 9/18 | INFO_REALIGN_3_PRIME | chrX | 70471023 | |||||
| chrX:70471078
|
A | G | 23 | a0001c0001t0001g0044a0001c0001t0001g0045a0001c0001t0001g0046others(20): Show | 23 | HG01081.hp2 HG01255.hp1 HG02280.hp2 others(20): Show |
intron_variant | MODIFIER | c.1406-8072A>G | DLG3 | ENSG00000082458.12 | transcript | ENST00000374360.8 | protein_coding | 9/18 | chrX | 70471078 | ||||||
| chrX:70471331
|
C | CT | 5 | a0001c0001t0001g0021a0001c0001t0001g0197a0001c0001t0001g0200others(2): Show | 5 | HG01069.hp1 HG02258.hp1 HG03017.hp1 others(2): Show |
intron_variant | MODIFIER | c.1406-7803dupT | DLG3 | ENSG00000082458.12 | transcript | ENST00000374360.8 | protein_coding | 9/18 | INFO_REALIGN_3_PRIME | chrX | 70471331 | |||||
| chrX:70471331
|
CT | C | 3 | a0001c0001t0002g0103a0001c0001t0002g0120a0001c0002t0005g0183 | 3 | HG01169.hp1 NA18948.hp1 NA19010.hp2 |
intron_variant | MODIFIER | c.1406-7803delT | DLG3 | ENSG00000082458.12 | transcript | ENST00000374360.8 | protein_coding | 9/18 | INFO_REALIGN_3_PRIME | chrX | 70471331 | |||||
| chrX:70471403
|
C | T | 1 | a0001c0001t0001g0029 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.1406-7747C>T | DLG3 | ENSG00000082458.12 | transcript | ENST00000374360.8 | protein_coding | 9/18 | chrX | 70471403 | ||||||
| chrX:70471416
|
G | A | 67 | a0001c0001t0001g0015a0001c0001t0001g0016a0001c0001t0001g0017others(64): Show | 74 | HG00733.hp1 HG00735.hp1 HG01070.hp2 others(71): Show |
intron_variant | MODIFIER | c.1406-7734G>A | DLG3 | ENSG00000082458.12 | transcript | ENST00000374360.8 | protein_coding | 9/18 | chrX | 70471416 | ||||||
| chrX:70471440
|
C | T | 1 | a0001c0001t0011g0043 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.1406-7710C>T | DLG3 | ENSG00000082458.12 | transcript | ENST00000374360.8 | protein_coding | 9/18 | chrX | 70471440 | ||||||
| chrX:70471491
|
G | A | 10 | a0001c0001t0002g0005a0001c0001t0002g0011a0001c0001t0002g0084others(7): Show | 13 | HG02083.hp1 NA18948.hp1 NA18949.hp1 others(10): Show |
intron_variant | MODIFIER | c.1406-7659G>A | DLG3 | ENSG00000082458.12 | transcript | ENST00000374360.8 | protein_coding | 9/18 | chrX | 70471491 | ||||||
| chrX:70471496
|
A | AT | 1 | a0001c0001t0001g0200 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.1406-7648dupT | DLG3 | ENSG00000082458.12 | transcript | ENST00000374360.8 | protein_coding | 9/18 | INFO_REALIGN_3_PRIME | chrX | 70471496 | |||||
| chrX:70471772
|
C | G | 1 | a0001c0001t0001g0029 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.1406-7378C>G | DLG3 | ENSG00000082458.12 | transcript | ENST00000374360.8 | protein_coding | 9/18 | chrX | 70471772 | ||||||
| chrX:70471866
|
A | G | 3 | a0001c0001t0002g0010a0001c0001t0002g0027a0001c0001t0002g0113 | 4 | HG02074.hp1 NA18947.hp1 NA18970.hp1 others(1): Show |
intron_variant | MODIFIER | c.1406-7284A>G | DLG3 | ENSG00000082458.12 | transcript | ENST00000374360.8 | protein_coding | 9/18 | chrX | 70471866 | ||||||
| chrX:70471885
|
G | A | 14 | a0001c0001t0001g0026a0001c0001t0001g0029a0001c0001t0001g0038others(11): Show | 15 | HG00099.hp1 HG00642.hp1 HG00733.hp2 others(12): Show |
intron_variant | MODIFIER | c.1406-7265G>A | DLG3 | ENSG00000082458.12 | transcript | ENST00000374360.8 | protein_coding | 9/18 | chrX | 70471885 | ||||||
| chrX:70472108
|
T | C | 117 | a0001c0001t0001g0015a0001c0001t0001g0016a0001c0001t0001g0017others(114): Show | 124 | HG00621.hp1 HG00733.hp1 HG00735.hp1 others(121): Show |
intron_variant | MODIFIER | c.1406-7042T>C | DLG3 | ENSG00000082458.12 | transcript | ENST00000374360.8 | protein_coding | 9/18 | chrX | 70472108 | ||||||
| chrX:70472257
|
CA | C | 1 | a0001c0001t0001g0161 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.1406-6887delA | DLG3 | ENSG00000082458.12 | transcript | ENST00000374360.8 | protein_coding | 9/18 | INFO_REALIGN_3_PRIME | chrX | 70472257 | |||||
| chrX:70472381
|
C | A | 1 | a0001c0001t0002g0077 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.1406-6769C>A | DLG3 | ENSG00000082458.12 | transcript | ENST00000374360.8 | protein_coding | 9/18 | chrX | 70472381 | ||||||
| chrX:70472486
|
C | T | 2 | a0001c0001t0001g0165a0001c0001t0030g0248 | 2 | HG03710.hp1 HG03927.hp2 |
intron_variant | MODIFIER | c.1406-6664C>T | DLG3 | ENSG00000082458.12 | transcript | ENST00000374360.8 | protein_coding | 9/18 | chrX | 70472486 | ||||||
| chrX:70472503
|
C | T | 1 | a0001c0001t0001g0025 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.1406-6647C>T | DLG3 | ENSG00000082458.12 | transcript | ENST00000374360.8 | protein_coding | 9/18 | chrX | 70472503 | ||||||
| chrX:70472506
|
G | C | 1 | a0001c0001t0012g0006 | 3 | HG00733.hp1 NA20752.hp1 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.1406-6644G>C | DLG3 | ENSG00000082458.12 | transcript | ENST00000374360.8 | protein_coding | 9/18 | chrX | 70472506 | ||||||
| chrX:70472600
|
T | A | 1 | a0001c0001t0002g0116 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.1406-6550T>A | DLG3 | ENSG00000082458.12 | transcript | ENST00000374360.8 | protein_coding | 9/18 | chrX | 70472600 | ||||||
| chrX:70472875
|
G | C | 6 | a0001c0002t0005g0039a0001c0002t0005g0040a0001c0002t0005g0041others(3): Show | 6 | HG01167.hp1 HG01169.hp1 HG02486.hp1 others(3): Show |
intron_variant | MODIFIER | c.1406-6275G>C | DLG3 | ENSG00000082458.12 | transcript | ENST00000374360.8 | protein_coding | 9/18 | chrX | 70472875 | ||||||
| chrX:70473138
|
CAA | C | 3 | a0001c0001t0001g0142a0001c0001t0001g0182a0001c0001t0001g0215 | 3 | HG00735.hp1 HG02647.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.1406-6011_1406-601 others(6): Show |
DLG3 | ENSG00000082458.12 | transcript | ENST00000374360.8 | protein_coding | 9/18 | chrX | 70473138 | ||||||
| chrX:70473157
|
C | CA | 19 | a0001c0001t0001g0023a0001c0001t0001g0024a0001c0001t0001g0145others(16): Show | 20 | HG00738.hp1 HG01261.hp1 HG01361.hp1 others(17): Show |
intron_variant | MODIFIER | c.1406-5972dupA | DLG3 | ENSG00000082458.12 | transcript | ENST00000374360.8 | protein_coding | 9/18 | INFO_REALIGN_3_PRIME | chrX | 70473157 | |||||
| chrX:70473157
|
C | CAA | 1 | a0001c0001t0001g0149 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.1406-5973_1406-597 others(6): Show |
DLG3 | ENSG00000082458.12 | transcript | ENST00000374360.8 | protein_coding | 9/18 | INFO_REALIGN_3_PRIME | chrX | 70473157 | |||||
| chrX:70473157
|
C | CAAA | 1 | a0001c0001t0001g0026 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1406-5974_1406-597 others(7): Show |
DLG3 | ENSG00000082458.12 | transcript | ENST00000374360.8 | protein_coding | 9/18 | INFO_REALIGN_3_PRIME | chrX | 70473157 | |||||
| chrX:70473157
|
CA | C | 99 | a0001c0001t0001g0015a0001c0001t0001g0016a0001c0001t0001g0017others(96): Show | 106 | HG00621.hp1 HG00733.hp1 HG00735.hp1 others(103): Show |
intron_variant | MODIFIER | c.1406-5972delA | DLG3 | ENSG00000082458.12 | transcript | ENST00000374360.8 | protein_coding | 9/18 | INFO_REALIGN_3_PRIME | chrX | 70473157 | |||||
| chrX:70473157
|
CAA | C | 1 | a0001c0001t0001g0228 | 1 | HG02897.hp1 | intron_variant | MODIFIER | c.1406-5973_1406-597 others(6): Show |
DLG3 | ENSG00000082458.12 | transcript | ENST00000374360.8 | protein_coding | 9/18 | INFO_REALIGN_3_PRIME | chrX | 70473157 | |||||
| chrX:70473403
|
C | T | 3 | a0001c0001t0002g0056a0001c0001t0002g0082a0001c0001t0002g0089 | 3 | HG00673.hp1 NA18957.hp2 NA18961.hp1 |
intron_variant | MODIFIER | c.1406-5747C>T | DLG3 | ENSG00000082458.12 | transcript | ENST00000374360.8 | protein_coding | 9/18 | chrX | 70473403 | ||||||
| chrX:70473405
|
T | C | 149 | a0001c0001t0001g0015a0001c0001t0001g0016a0001c0001t0001g0017others(146): Show | 157 | HG00099.hp1 HG00621.hp1 HG00642.hp1 others(154): Show |
intron_variant | MODIFIER | c.1406-5745T>C | DLG3 | ENSG00000082458.12 | transcript | ENST00000374360.8 | protein_coding | 9/18 | chrX | 70473405 | ||||||
| chrX:70473443
|
C | T | 1 | a0001c0001t0010g0186 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.1406-5707C>T | DLG3 | ENSG00000082458.12 | transcript | ENST00000374360.8 | protein_coding | 9/18 | chrX | 70473443 | ||||||
| chrX:70474351
|
GA | G | 19 | a0001c0001t0001g0023a0001c0001t0001g0024a0001c0001t0001g0145others(16): Show | 19 | HG00738.hp1 HG01167.hp1 HG01169.hp1 others(16): Show |
intron_variant | MODIFIER | c.1406-4795delA | DLG3 | ENSG00000082458.12 | transcript | ENST00000374360.8 | protein_coding | 9/18 | INFO_REALIGN_3_PRIME | chrX | 70474351 | |||||
| chrX:70474612
|
G | A | 1 | a0001c0001t0001g0026 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1406-4538G>A | DLG3 | ENSG00000082458.12 | transcript | ENST00000374360.8 | protein_coding | 9/18 | chrX | 70474612 | ||||||
| chrX:70474707
|
A | T | 23 | a0001c0001t0001g0044a0001c0001t0001g0045a0001c0001t0001g0046others(20): Show | 23 | HG01081.hp2 HG01255.hp1 HG02280.hp2 others(20): Show |
intron_variant | MODIFIER | c.1406-4443A>T | DLG3 | ENSG00000082458.12 | transcript | ENST00000374360.8 | protein_coding | 9/18 | chrX | 70474707 | ||||||
| chrX:70474712
|
G | C | 1 | a0001c0001t0002g0116 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.1406-4438G>C | DLG3 | ENSG00000082458.12 | transcript | ENST00000374360.8 | protein_coding | 9/18 | chrX | 70474712 | ||||||
| chrX:70474972
|
T | C | 1 | a0001c0001t0002g0116 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.1406-4178T>C | DLG3 | ENSG00000082458.12 | transcript | ENST00000374360.8 | protein_coding | 9/18 | chrX | 70474972 | ||||||
| chrX:70475002
|
T | C | 3 | a0001c0001t0001g0149a0001c0001t0001g0150a0001c0001t0001g0151 | 3 | NA19002.hp2 NA19011.hp1 NA19074.hp1 |
intron_variant | MODIFIER | c.1406-4148T>C | DLG3 | ENSG00000082458.12 | transcript | ENST00000374360.8 | protein_coding | 9/18 | chrX | 70475002 | ||||||
| chrX:70475188
|
C | CA | 1 | a0001c0001t0004g0222 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.1406-3953dupA | DLG3 | ENSG00000082458.12 | transcript | ENST00000374360.8 | protein_coding | 9/18 | INFO_REALIGN_3_PRIME | chrX | 70475188 | |||||
| chrX:70475188
|
CA | C | 6 | a0001c0002t0005g0039a0001c0002t0005g0040a0001c0002t0005g0041others(3): Show | 6 | HG01167.hp1 HG01169.hp1 HG02486.hp1 others(3): Show |
intron_variant | MODIFIER | c.1406-3953delA | DLG3 | ENSG00000082458.12 | transcript | ENST00000374360.8 | protein_coding | 9/18 | INFO_REALIGN_3_PRIME | chrX | 70475188 | |||||
| chrX:70475197
|
A | C | 2 | a0001c0001t0002g0056a0001c0001t0002g0089 | 2 | NA18957.hp2 NA18961.hp1 |
intron_variant | MODIFIER | c.1406-3953A>C | DLG3 | ENSG00000082458.12 | transcript | ENST00000374360.8 | protein_coding | 9/18 | chrX | 70475197 | ||||||
| chrX:70475224
|
T | C | 1 | a0001c0001t0001g0038 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.1406-3926T>C | DLG3 | ENSG00000082458.12 | transcript | ENST00000374360.8 | protein_coding | 9/18 | chrX | 70475224 | ||||||
| chrX:70475522
|
C | G | 1 | a0001c0001t0001g0205 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.1406-3628C>G | DLG3 | ENSG00000082458.12 | transcript | ENST00000374360.8 | protein_coding | 9/18 | chrX | 70475522 | ||||||
| chrX:70475653
|
G | A | 2 | a0001c0001t0001g0205a0001c0001t0001g0241 | 2 | HG02615.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.1406-3497G>A | DLG3 | ENSG00000082458.12 | transcript | ENST00000374360.8 | protein_coding | 9/18 | chrX | 70475653 | ||||||
| chrX:70475800
|
T | A | 1 | a0001c0001t0005g0037 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.1406-3350T>A | DLG3 | ENSG00000082458.12 | transcript | ENST00000374360.8 | protein_coding | 9/18 | chrX | 70475800 | ||||||
| chrX:70475903
|
C | G | 4 | a0001c0001t0001g0134a0001c0001t0001g0165a0001c0001t0001g0219others(1): Show | 4 | HG03491.hp1 HG03492.hp1 HG03710.hp1 others(1): Show |
intron_variant | MODIFIER | c.1406-3247C>G | DLG3 | ENSG00000082458.12 | transcript | ENST00000374360.8 | protein_coding | 9/18 | chrX | 70475903 | ||||||
| chrX:70475947
|
G | T | 10 | a0001c0001t0003g0008a0001c0001t0003g0028a0001c0001t0003g0030others(7): Show | 11 | HG00099.hp1 HG00642.hp1 HG00733.hp2 others(8): Show |
intron_variant | MODIFIER | c.1406-3203G>T | DLG3 | ENSG00000082458.12 | transcript | ENST00000374360.8 | protein_coding | 9/18 | chrX | 70475947 | ||||||
| chrX:70475963
|
A | C | 2 | a0001c0001t0024g0052a0001c0001t0027g0051 | 2 | HG01081.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.1406-3187A>C | DLG3 | ENSG00000082458.12 | transcript | ENST00000374360.8 | protein_coding | 9/18 | chrX | 70475963 | ||||||
| chrX:70476196
|
G | A | 28 | a0001c0001t0001g0015a0001c0001t0001g0016a0001c0001t0001g0025others(25): Show | 32 | HG01109.hp1 HG01123.hp1 HG01257.hp1 others(29): Show |
intron_variant | MODIFIER | c.1406-2954G>A | DLG3 | ENSG00000082458.12 | transcript | ENST00000374360.8 | protein_coding | 9/18 | chrX | 70476196 | ||||||
| chrX:70476210
|
T | G | 6 | a0001c0002t0005g0039a0001c0002t0005g0040a0001c0002t0005g0041others(3): Show | 6 | HG01167.hp1 HG01169.hp1 HG02486.hp1 others(3): Show |
intron_variant | MODIFIER | c.1406-2940T>G | DLG3 | ENSG00000082458.12 | transcript | ENST00000374360.8 | protein_coding | 9/18 | chrX | 70476210 | ||||||
| chrX:70476476
|
C | T | 1 | a0001c0001t0001g0059 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.1406-2674C>T | DLG3 | ENSG00000082458.12 | transcript | ENST00000374360.8 | protein_coding | 9/18 | chrX | 70476476 | ||||||
| chrX:70476899
|
C | T | 22 | a0001c0001t0001g0044a0001c0001t0001g0045a0001c0001t0001g0046others(19): Show | 22 | HG01081.hp2 HG01255.hp1 HG02280.hp2 others(19): Show |
intron_variant | MODIFIER | c.1406-2251C>T | DLG3 | ENSG00000082458.12 | transcript | ENST00000374360.8 | protein_coding | 9/18 | chrX | 70476899 | ||||||
| chrX:70476989
|
C | T | 2 | a0001c0001t0001g0173a0001c0001t0001g0174 | 2 | HG01255.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.1406-2161C>T | DLG3 | ENSG00000082458.12 | transcript | ENST00000374360.8 | protein_coding | 9/18 | chrX | 70476989 | ||||||
| chrX:70477055
|
G | A | 3 | a0001c0001t0001g0137a0001c0001t0001g0235a0001c0001t0001g0236 | 3 | HG03453.hp2 HG03471.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.1406-2095G>A | DLG3 | ENSG00000082458.12 | transcript | ENST00000374360.8 | protein_coding | 9/18 | chrX | 70477055 | ||||||
| chrX:70477421
|
C | G | 1 | a0001c0001t0001g0029 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.1406-1729C>G | DLG3 | ENSG00000082458.12 | transcript | ENST00000374360.8 | protein_coding | 9/18 | chrX | 70477421 | ||||||
| chrX:70478128
|
C | T | 1 | a0001c0001t0001g0020 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.1406-1022C>T | DLG3 | ENSG00000082458.12 | transcript | ENST00000374360.8 | protein_coding | 9/18 | chrX | 70478128 | ||||||
| chrX:70478305
|
G | A | 149 | a0001c0001t0001g0015a0001c0001t0001g0016a0001c0001t0001g0017others(146): Show | 157 | HG00099.hp1 HG00621.hp1 HG00642.hp1 others(154): Show |
intron_variant | MODIFIER | c.1406-845G>A | DLG3 | ENSG00000082458.12 | transcript | ENST00000374360.8 | protein_coding | 9/18 | chrX | 70478305 | ||||||
| chrX:70478355
|
G | C | 1 | a0001c0001t0022g0227 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.1406-795G>C | DLG3 | ENSG00000082458.12 | transcript | ENST00000374360.8 | protein_coding | 9/18 | chrX | 70478355 | ||||||
| chrX:70478585
|
G | GT | 1 | a0001c0001t0001g0204 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.1406-562dupT | DLG3 | ENSG00000082458.12 | transcript | ENST00000374360.8 | protein_coding | 9/18 | INFO_REALIGN_3_PRIME | chrX | 70478585 | |||||
| chrX:70478613
|
T | C | 1 | a0001c0001t0002g0054 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.1406-537T>C | DLG3 | ENSG00000082458.12 | transcript | ENST00000374360.8 | protein_coding | 9/18 | chrX | 70478613 | ||||||
| chrX:70478677
|
A | G | 1 | a0001c0001t0019g0141 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1406-473A>G | DLG3 | ENSG00000082458.12 | transcript | ENST00000374360.8 | protein_coding | 9/18 | chrX | 70478677 | ||||||
| chrX:70478804
|
A | T | 8 | a0001c0001t0002g0012a0001c0001t0002g0064a0001c0001t0002g0094others(5): Show | 9 | HG00099.hp2 HG00741.hp2 HG01074.hp1 others(6): Show |
intron_variant | MODIFIER | c.1406-346A>T | DLG3 | ENSG00000082458.12 | transcript | ENST00000374360.8 | protein_coding | 9/18 | chrX | 70478804 | ||||||
| chrX:70478873
|
C | T | 149 | a0001c0001t0001g0015a0001c0001t0001g0016a0001c0001t0001g0017others(146): Show | 157 | HG00099.hp1 HG00621.hp1 HG00642.hp1 others(154): Show |
intron_variant | MODIFIER | c.1406-277C>T | DLG3 | ENSG00000082458.12 | transcript | ENST00000374360.8 | protein_coding | 9/18 | chrX | 70478873 | ||||||
| chrX:70479061
|
C | G | 1 | a0001c0001t0002g0114 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.1406-89C>G | DLG3 | ENSG00000082458.12 | transcript | ENST00000374360.8 | protein_coding | 9/18 | chrX | 70479061 | ||||||
| chrX:70479101
|
G | A | 1 | a0001c0001t0001g0026 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1406-49G>A | DLG3 | ENSG00000082458.12 | transcript | ENST00000374360.8 | protein_coding | 9/18 | chrX | 70479101 | ||||||
| chrX:70479115
|
TTCTTTTC others(3): Show |
T | 1 | a0001c0001t0001g0029 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.1406-25_1406-16del others(10): Show |
DLG3 | ENSG00000082458.12 | transcript | ENST00000374360.8 | protein_coding | 9/18 | INFO_REALIGN_3_PRIME | chrX | 70479115 | |||||
| chrX:70479282
|
G | A | 2 | a0001c0001t0002g0095a0001c0001t0008g0073 | 2 | NA18964.hp1 NA18994.hp1 |
intron_variant | MODIFIER | c.1520+18G>A | DLG3 | ENSG00000082458.12 | transcript | ENST00000374360.8 | protein_coding | 10/18 | chrX | 70479282 | ||||||
| chrX:70479283
|
C | A | 2 | a0001c0001t0002g0095a0001c0001t0008g0073 | 2 | NA18964.hp1 NA18994.hp1 |
intron_variant | MODIFIER | c.1520+19C>A | DLG3 | ENSG00000082458.12 | transcript | ENST00000374360.8 | protein_coding | 10/18 | chrX | 70479283 | ||||||
| chrX:70479604
|
A | AC | 15 | a0001c0001t0001g0045a0001c0001t0001g0196a0001c0001t0002g0067others(12): Show | 15 | HG00642.hp1 HG00735.hp2 HG02055.hp1 others(12): Show |
intron_variant | MODIFIER | c.1520+347dupC | DLG3 | ENSG00000082458.12 | transcript | ENST00000374360.8 | protein_coding | 10/18 | INFO_REALIGN_3_PRIME | chrX | 70479604 | |||||
| chrX:70479740
|
T | C | 1 | a0001c0001t0020g0218 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.1520+476T>C | DLG3 | ENSG00000082458.12 | transcript | ENST00000374360.8 | protein_coding | 10/18 | chrX | 70479740 | ||||||
| chrX:70479792
|
A | G | 2 | a0001c0001t0011g0214a0001c0001t0011g0242 | 2 | HG03540.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.1520+528A>G | DLG3 | ENSG00000082458.12 | transcript | ENST00000374360.8 | protein_coding | 10/18 | chrX | 70479792 | ||||||
| chrX:70479806
|
G | C | 2 | a0001c0001t0001g0173a0001c0001t0001g0174 | 2 | HG01255.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.1520+542G>C | DLG3 | ENSG00000082458.12 | transcript | ENST00000374360.8 | protein_coding | 10/18 | chrX | 70479806 | ||||||
| chrX:70479827
|
A | G | 2 | a0001c0001t0001g0173a0001c0001t0001g0174 | 2 | HG01255.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.1520+563A>G | DLG3 | ENSG00000082458.12 | transcript | ENST00000374360.8 | protein_coding | 10/18 | chrX | 70479827 | ||||||
| chrX:70479891
|
A | G | 151 | a0001c0001t0001g0015a0001c0001t0001g0016a0001c0001t0001g0017others(148): Show | 159 | HG00099.hp1 HG00621.hp1 HG00642.hp1 others(156): Show |
intron_variant | MODIFIER | c.1520+627A>G | DLG3 | ENSG00000082458.12 | transcript | ENST00000374360.8 | protein_coding | 10/18 | chrX | 70479891 | ||||||
| chrX:70480198
|
C | G | 2 | a0001c0001t0001g0209a0001c0001t0001g0213 | 2 | HG02809.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.1520+934C>G | DLG3 | ENSG00000082458.12 | transcript | ENST00000374360.8 | protein_coding | 10/18 | chrX | 70480198 | ||||||
| chrX:70480200
|
G | A | 26 | a0001c0001t0001g0019a0001c0001t0001g0058a0001c0001t0001g0059others(23): Show | 26 | HG00621.hp1 HG02015.hp1 HG02155.hp2 others(23): Show |
intron_variant | MODIFIER | c.1520+936G>A | DLG3 | ENSG00000082458.12 | transcript | ENST00000374360.8 | protein_coding | 10/18 | chrX | 70480200 | ||||||
| chrX:70480458
|
T | G | 136 | a0001c0001t0001g0015a0001c0001t0001g0016a0001c0001t0001g0017others(133): Show | 143 | HG00621.hp1 HG00733.hp1 HG00735.hp1 others(140): Show |
intron_variant | MODIFIER | c.1520+1194T>G | DLG3 | ENSG00000082458.12 | transcript | ENST00000374360.8 | protein_coding | 10/18 | chrX | 70480458 | ||||||
| chrX:70480540
|
G | A | 150 | a0001c0001t0001g0015a0001c0001t0001g0016a0001c0001t0001g0017others(147): Show | 158 | HG00099.hp1 HG00621.hp1 HG00642.hp1 others(155): Show |
intron_variant | MODIFIER | c.1520+1276G>A | DLG3 | ENSG00000082458.12 | transcript | ENST00000374360.8 | protein_coding | 10/18 | chrX | 70480540 | ||||||
| chrX:70480657
|
GA | G | 1 | a0001c0001t0001g0135 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.1520+1396delA | DLG3 | ENSG00000082458.12 | transcript | ENST00000374360.8 | protein_coding | 10/18 | INFO_REALIGN_3_PRIME | chrX | 70480657 | |||||
| chrX:70480885
|
G | A | 3 | a0001c0001t0001g0047a0001c0001t0001g0048a0001c0001t0001g0049 | 3 | HG02622.hp2 HG03130.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.1520+1621G>A | DLG3 | ENSG00000082458.12 | transcript | ENST00000374360.8 | protein_coding | 10/18 | chrX | 70480885 | ||||||
| chrX:70480949
|
G | C | 1 | a0001c0001t0002g0101 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.1520+1685G>C | DLG3 | ENSG00000082458.12 | transcript | ENST00000374360.8 | protein_coding | 10/18 | chrX | 70480949 | ||||||
| chrX:70481256
|
T | G | 1 | a0001c0001t0004g0221 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.1520+1992T>G | DLG3 | ENSG00000082458.12 | transcript | ENST00000374360.8 | protein_coding | 10/18 | chrX | 70481256 | ||||||
| chrX:70481518
|
C | T | 7 | a0001c0001t0002g0054a0001c0001t0002g0075a0001c0001t0002g0076others(4): Show | 7 | HG00609.hp1 HG02165.hp2 HG03491.hp2 others(4): Show |
intron_variant | MODIFIER | c.1520+2254C>T | DLG3 | ENSG00000082458.12 | transcript | ENST00000374360.8 | protein_coding | 10/18 | chrX | 70481518 | ||||||
| chrX:70481553
|
C | T | 14 | a0001c0001t0001g0029a0001c0001t0001g0038a0001c0001t0001g0204others(11): Show | 15 | HG00099.hp1 HG00642.hp1 HG00733.hp2 others(12): Show |
intron_variant | MODIFIER | c.1520+2289C>T | DLG3 | ENSG00000082458.12 | transcript | ENST00000374360.8 | protein_coding | 10/18 | chrX | 70481553 | ||||||
| chrX:70481879
|
C | G | 1 | a0001c0001t0001g0047 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.1520+2615C>G | DLG3 | ENSG00000082458.12 | transcript | ENST00000374360.8 | protein_coding | 10/18 | chrX | 70481879 | ||||||
| chrX:70482010
|
C | T | 1 | a0001c0001t0001g0020 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.1520+2746C>T | DLG3 | ENSG00000082458.12 | transcript | ENST00000374360.8 | protein_coding | 10/18 | chrX | 70482010 | ||||||
| chrX:70482169
|
T | C | 2 | a0001c0001t0001g0135a0001c0001t0001g0193 | 2 | NA18955.hp1 NA18957.hp1 |
intron_variant | MODIFIER | c.1520+2905T>C | DLG3 | ENSG00000082458.12 | transcript | ENST00000374360.8 | protein_coding | 10/18 | chrX | 70482169 | ||||||
| chrX:70482180
|
C | T | 2 | a0001c0001t0001g0206a0001c0001t0001g0216 | 2 | HG01243.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.1520+2916C>T | DLG3 | ENSG00000082458.12 | transcript | ENST00000374360.8 | protein_coding | 10/18 | chrX | 70482180 | ||||||
| chrX:70482216
|
G | A | 1 | a0001c0001t0002g0014 | 2 | HG00140.hp1 HG01081.hp1 |
intron_variant | MODIFIER | c.1520+2952G>A | DLG3 | ENSG00000082458.12 | transcript | ENST00000374360.8 | protein_coding | 10/18 | chrX | 70482216 | ||||||
| chrX:70482258
|
A | AG | 1 | a0001c0001t0001g0189 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.1520+2999dupG | DLG3 | ENSG00000082458.12 | transcript | ENST00000374360.8 | protein_coding | 10/18 | INFO_REALIGN_3_PRIME | chrX | 70482258 | |||||
| chrX:70482408
|
T | G | 1 | a0001c0001t0001g0059 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.1520+3144T>G | DLG3 | ENSG00000082458.12 | transcript | ENST00000374360.8 | protein_coding | 10/18 | chrX | 70482408 | ||||||
| chrX:70482433
|
ATAT | A | 1 | a0001c0001t0002g0081 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.1520+3173_1520+317 others(7): Show |
DLG3 | ENSG00000082458.12 | transcript | ENST00000374360.8 | protein_coding | 10/18 | INFO_REALIGN_3_PRIME | chrX | 70482433 | |||||
| chrX:70482659
|
G | GTTTTT | 1 | a0001c0001t0001g0017 | 2 | HG02257.hp1 HG02965.hp1 |
intron_variant | MODIFIER | c.1520+3395_1520+339 others(9): Show |
DLG3 | ENSG00000082458.12 | transcript | ENST00000374360.8 | protein_coding | 10/18 | chrX | 70482659 | ||||||
| chrX:70482660
|
G | GT | 1 | a0001c0001t0001g0140 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.1520+3397dupT | DLG3 | ENSG00000082458.12 | transcript | ENST00000374360.8 | protein_coding | 10/18 | INFO_REALIGN_3_PRIME | chrX | 70482660 | |||||
| chrX:70482660
|
G | GTTTT | 2 | a0001c0001t0001g0209a0001c0001t0001g0249 | 2 | HG02809.hp1 NA18968.hp1 |
intron_variant | MODIFIER | c.1520+3397_1520+339 others(8): Show |
DLG3 | ENSG00000082458.12 | transcript | ENST00000374360.8 | protein_coding | 10/18 | INFO_REALIGN_3_PRIME | chrX | 70482660 | |||||
| chrX:70482660
|
G | GTTTTT | 42 | a0001c0001t0001g0015a0001c0001t0001g0019a0001c0001t0001g0020others(39): Show | 45 | HG00733.hp1 HG01070.hp2 HG01192.hp1 others(42): Show |
intron_variant | MODIFIER | c.1520+3397_1520+339 others(9): Show |
DLG3 | ENSG00000082458.12 | transcript | ENST00000374360.8 | protein_coding | 10/18 | INFO_REALIGN_3_PRIME | chrX | 70482660 | |||||
| chrX:70482660
|
G | GTTTTTT | 34 | a0001c0001t0001g0022a0001c0001t0001g0025a0001c0001t0001g0053others(31): Show | 36 | HG00621.hp1 HG00735.hp1 HG01106.hp1 others(33): Show |
intron_variant | MODIFIER | c.1520+3397_1520+339 others(10): Show |
DLG3 | ENSG00000082458.12 | transcript | ENST00000374360.8 | protein_coding | 10/18 | INFO_REALIGN_3_PRIME | chrX | 70482660 | |||||
| chrX:70482660
|
G | GTTTTTTT | 7 | a0001c0001t0001g0016a0001c0001t0001g0155a0001c0001t0001g0160others(4): Show | 8 | HG01516.hp2 HG03540.hp2 NA18747.hp1 others(5): Show |
intron_variant | MODIFIER | c.1520+3397_1520+339 others(11): Show |
DLG3 | ENSG00000082458.12 | transcript | ENST00000374360.8 | protein_coding | 10/18 | INFO_REALIGN_3_PRIME | chrX | 70482660 | |||||
| chrX:70482660
|
G | GTTTTTTT others(1): Show |
2 | a0001c0001t0001g0164a0001c0001t0001g0189 | 2 | HG01928.hp1 NA18967.hp1 |
intron_variant | MODIFIER | c.1520+3397_1520+339 others(12): Show |
DLG3 | ENSG00000082458.12 | transcript | ENST00000374360.8 | protein_coding | 10/18 | INFO_REALIGN_3_PRIME | chrX | 70482660 | |||||
| chrX:70482660
|
G | T | 1 | a0001c0001t0001g0017 | 2 | HG02257.hp1 HG02965.hp1 |
intron_variant | MODIFIER | c.1520+3396G>T | DLG3 | ENSG00000082458.12 | transcript | ENST00000374360.8 | protein_coding | 10/18 | chrX | 70482660 | ||||||
| chrX:70482660
|
GTGTTTTT | G | 1 | a0001c0001t0019g0141 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1520+3398_1520+340 others(11): Show |
DLG3 | ENSG00000082458.12 | transcript | ENST00000374360.8 | protein_coding | 10/18 | INFO_REALIGN_3_PRIME | chrX | 70482660 | |||||
| chrX:70482662
|
G | GT | 11 | a0001c0001t0002g0080a0001c0001t0002g0084a0001c0001t0002g0088others(8): Show | 11 | HG02071.hp1 HG03098.hp1 HG03704.hp2 others(8): Show |
intron_variant | MODIFIER | c.1520+3421dupT | DLG3 | ENSG00000082458.12 | transcript | ENST00000374360.8 | protein_coding | 10/18 | INFO_REALIGN_3_PRIME | chrX | 70482662 | |||||
| chrX:70482662
|
G | GTT | 3 | a0001c0001t0001g0026a0001c0001t0004g0232a0005c0008t0002g0129 | 3 | HG02257.hp2 NA18988.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.1520+3420_1520+342 others(6): Show |
DLG3 | ENSG00000082458.12 | transcript | ENST00000374360.8 | protein_coding | 10/18 | INFO_REALIGN_3_PRIME | chrX | 70482662 | |||||
| chrX:70482662
|
G | GTTTT | 2 | a0001c0001t0001g0174a0001c0001t0011g0043 | 2 | HG02976.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.1520+3418_1520+342 others(8): Show |
DLG3 | ENSG00000082458.12 | transcript | ENST00000374360.8 | protein_coding | 10/18 | INFO_REALIGN_3_PRIME | chrX | 70482662 | |||||
| chrX:70482662
|
G | GTTTTT | 13 | a0001c0001t0001g0044a0001c0001t0001g0046a0001c0001t0001g0047others(10): Show | 13 | HG01081.hp2 HG02451.hp1 HG02559.hp1 others(10): Show |
intron_variant | MODIFIER | c.1520+3417_1520+342 others(9): Show |
DLG3 | ENSG00000082458.12 | transcript | ENST00000374360.8 | protein_coding | 10/18 | INFO_REALIGN_3_PRIME | chrX | 70482662 | |||||
| chrX:70482662
|
G | GTTTTTT | 7 | a0001c0001t0001g0045a0001c0001t0001g0173a0001c0001t0001g0230others(4): Show | 7 | HG01255.hp1 HG02280.hp2 HG02572.hp1 others(4): Show |
intron_variant | MODIFIER | c.1520+3416_1520+342 others(10): Show |
DLG3 | ENSG00000082458.12 | transcript | ENST00000374360.8 | protein_coding | 10/18 | INFO_REALIGN_3_PRIME | chrX | 70482662 | |||||
| chrX:70482662
|
G | GTTTTTTT others(3): Show |
1 | a0001c0001t0001g0038 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.1520+3412_1520+342 others(14): Show |
DLG3 | ENSG00000082458.12 | transcript | ENST00000374360.8 | protein_coding | 10/18 | INFO_REALIGN_3_PRIME | chrX | 70482662 | |||||
| chrX:70482662
|
G | GTTTTTTT others(4): Show |
5 | a0001c0001t0003g0008a0001c0001t0003g0028a0001c0001t0003g0031others(2): Show | 6 | HG00099.hp1 HG01069.hp1 HG01070.hp1 others(3): Show |
intron_variant | MODIFIER | c.1520+3411_1520+342 others(15): Show |
DLG3 | ENSG00000082458.12 | transcript | ENST00000374360.8 | protein_coding | 10/18 | INFO_REALIGN_3_PRIME | chrX | 70482662 | |||||
| chrX:70482662
|
G | GTTTTTTT others(5): Show |
5 | a0001c0001t0003g0032a0001c0001t0003g0036a0001c0001t0003g0156others(2): Show | 5 | HG00733.hp2 HG01123.hp2 HG01891.hp1 others(2): Show |
intron_variant | MODIFIER | c.1520+3410_1520+342 others(16): Show |
DLG3 | ENSG00000082458.12 | transcript | ENST00000374360.8 | protein_coding | 10/18 | INFO_REALIGN_3_PRIME | chrX | 70482662 | |||||
| chrX:70482662
|
G | GTTTTTTT others(6): Show |
2 | a0001c0001t0003g0030a0001c0001t0003g0033 | 2 | HG00642.hp1 HG01993.hp2 |
intron_variant | MODIFIER | c.1520+3409_1520+342 others(17): Show |
DLG3 | ENSG00000082458.12 | transcript | ENST00000374360.8 | protein_coding | 10/18 | INFO_REALIGN_3_PRIME | chrX | 70482662 | |||||
| chrX:70482662
|
G | T | 89 | a0001c0001t0001g0015a0001c0001t0001g0016a0001c0001t0001g0017others(86): Show | 96 | HG00621.hp1 HG00733.hp1 HG00735.hp1 others(93): Show |
intron_variant | MODIFIER | c.1520+3398G>T | DLG3 | ENSG00000082458.12 | transcript | ENST00000374360.8 | protein_coding | 10/18 | chrX | 70482662 | ||||||
| chrX:70482662
|
GTTT | G | 5 | a0001c0001t0001g0029a0001c0001t0001g0146a0001c0001t0001g0185others(2): Show | 5 | HG00738.hp1 HG02280.hp1 HG02630.hp2 others(2): Show |
intron_variant | MODIFIER | c.1520+3419_1520+342 others(7): Show |
DLG3 | ENSG00000082458.12 | transcript | ENST00000374360.8 | protein_coding | 10/18 | INFO_REALIGN_3_PRIME | chrX | 70482662 | |||||
| chrX:70482662
|
GTTTT | G | 17 | a0001c0001t0001g0023a0001c0001t0001g0024a0001c0001t0001g0145others(14): Show | 17 | HG01167.hp1 HG01169.hp1 HG01261.hp1 others(14): Show |
intron_variant | MODIFIER | c.1520+3418_1520+342 others(8): Show |
DLG3 | ENSG00000082458.12 | transcript | ENST00000374360.8 | protein_coding | 10/18 | INFO_REALIGN_3_PRIME | chrX | 70482662 | |||||
| chrX:70482670
|
T | G | 1 | a0001c0001t0002g0114 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.1520+3406T>G | DLG3 | ENSG00000082458.12 | transcript | ENST00000374360.8 | protein_coding | 10/18 | chrX | 70482670 | ||||||
| chrX:70482800
|
T | TG | 1 | a0001c0001t0001g0189 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.1520+3539dupG | DLG3 | ENSG00000082458.12 | transcript | ENST00000374360.8 | protein_coding | 10/18 | INFO_REALIGN_3_PRIME | chrX | 70482800 | |||||
| chrX:70482857
|
C | T | 1 | a0001c0001t0001g0204 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.1520+3593C>T | DLG3 | ENSG00000082458.12 | transcript | ENST00000374360.8 | protein_coding | 10/18 | chrX | 70482857 | ||||||
| chrX:70482924
|
C | T | 148 | a0001c0001t0001g0015a0001c0001t0001g0016a0001c0001t0001g0017others(145): Show | 156 | HG00099.hp1 HG00621.hp1 HG00642.hp1 others(153): Show |
intron_variant | MODIFIER | c.1520+3660C>T | DLG3 | ENSG00000082458.12 | transcript | ENST00000374360.8 | protein_coding | 10/18 | chrX | 70482924 | ||||||
| chrX:70482926
|
C | T | 148 | a0001c0001t0001g0015a0001c0001t0001g0016a0001c0001t0001g0017others(145): Show | 156 | HG00099.hp1 HG00621.hp1 HG00642.hp1 others(153): Show |
intron_variant | MODIFIER | c.1520+3662C>T | DLG3 | ENSG00000082458.12 | transcript | ENST00000374360.8 | protein_coding | 10/18 | chrX | 70482926 | ||||||
| chrX:70482956
|
C | T | 1 | a0001c0001t0003g0032 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.1520+3692C>T | DLG3 | ENSG00000082458.12 | transcript | ENST00000374360.8 | protein_coding | 10/18 | chrX | 70482956 | ||||||
| chrX:70482959
|
G | GC | 1 | a0001c0001t0001g0189 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.1520+3698dupC | DLG3 | ENSG00000082458.12 | transcript | ENST00000374360.8 | protein_coding | 10/18 | INFO_REALIGN_3_PRIME | chrX | 70482959 | |||||
| chrX:70483001
|
C | G | 19 | a0001c0001t0001g0023a0001c0001t0001g0024a0001c0001t0001g0145others(16): Show | 19 | HG00738.hp1 HG01167.hp1 HG01169.hp1 others(16): Show |
intron_variant | MODIFIER | c.1520+3737C>G | DLG3 | ENSG00000082458.12 | transcript | ENST00000374360.8 | protein_coding | 10/18 | chrX | 70483001 | ||||||
| chrX:70483020
|
C | G | 3 | a0001c0001t0002g0060a0001c0001t0002g0067a0001c0001t0006g0109 | 3 | HG00735.hp2 HG01346.hp2 HG03669.hp2 |
intron_variant | MODIFIER | c.1520+3756C>G | DLG3 | ENSG00000082458.12 | transcript | ENST00000374360.8 | protein_coding | 10/18 | chrX | 70483020 | ||||||
| chrX:70483217
|
G | A | 90 | a0001c0001t0001g0015a0001c0001t0001g0016a0001c0001t0001g0017others(87): Show | 97 | HG00621.hp1 HG00733.hp1 HG00735.hp1 others(94): Show |
intron_variant | MODIFIER | c.1520+3953G>A | DLG3 | ENSG00000082458.12 | transcript | ENST00000374360.8 | protein_coding | 10/18 | chrX | 70483217 | ||||||
| chrX:70483432
|
A | G | 1 | a0001c0001t0004g0222 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.1520+4168A>G | DLG3 | ENSG00000082458.12 | transcript | ENST00000374360.8 | protein_coding | 10/18 | chrX | 70483432 | ||||||
| chrX:70483455
|
G | A | 148 | a0001c0001t0001g0015a0001c0001t0001g0016a0001c0001t0001g0017others(145): Show | 156 | HG00099.hp1 HG00621.hp1 HG00642.hp1 others(153): Show |
intron_variant | MODIFIER | c.1520+4191G>A | DLG3 | ENSG00000082458.12 | transcript | ENST00000374360.8 | protein_coding | 10/18 | chrX | 70483455 | ||||||
| chrX:70483895
|
G | A | 2 | a0001c0001t0002g0067a0001c0001t0006g0109 | 2 | HG00735.hp2 HG03669.hp2 |
intron_variant | MODIFIER | c.1520+4631G>A | DLG3 | ENSG00000082458.12 | transcript | ENST00000374360.8 | protein_coding | 10/18 | chrX | 70483895 | ||||||
| chrX:70484062
|
T | TATTTA | 3 | a0001c0001t0001g0026a0001c0001t0001g0208a0001c0001t0022g0227 | 3 | HG02886.hp2 HG03579.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.1520+4824_1520+482 others(9): Show |
DLG3 | ENSG00000082458.12 | transcript | ENST00000374360.8 | protein_coding | 10/18 | INFO_REALIGN_3_PRIME | chrX | 70484062 | |||||
| chrX:70484062
|
T | TATTTAAT others(3): Show |
1 | a0001c0001t0001g0133 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.1520+4819_1520+482 others(14): Show |
DLG3 | ENSG00000082458.12 | transcript | ENST00000374360.8 | protein_coding | 10/18 | INFO_REALIGN_3_PRIME | chrX | 70484062 | |||||
| chrX:70484275
|
C | T | 90 | a0001c0001t0001g0015a0001c0001t0001g0016a0001c0001t0001g0017others(87): Show | 97 | HG00621.hp1 HG00733.hp1 HG00735.hp1 others(94): Show |
intron_variant | MODIFIER | c.1520+5011C>T | DLG3 | ENSG00000082458.12 | transcript | ENST00000374360.8 | protein_coding | 10/18 | chrX | 70484275 | ||||||
| chrX:70484481
|
T | G | 149 | a0001c0001t0001g0015a0001c0001t0001g0016a0001c0001t0001g0017others(146): Show | 157 | HG00099.hp1 HG00621.hp1 HG00642.hp1 others(154): Show |
intron_variant | MODIFIER | c.1520+5217T>G | DLG3 | ENSG00000082458.12 | transcript | ENST00000374360.8 | protein_coding | 10/18 | chrX | 70484481 | ||||||
| chrX:70484521
|
G | T | 148 | a0001c0001t0001g0015a0001c0001t0001g0016a0001c0001t0001g0017others(145): Show | 156 | HG00099.hp1 HG00621.hp1 HG00642.hp1 others(153): Show |
intron_variant | MODIFIER | c.1520+5257G>T | DLG3 | ENSG00000082458.12 | transcript | ENST00000374360.8 | protein_coding | 10/18 | chrX | 70484521 | ||||||
| chrX:70484852
|
A | G | 2 | a0001c0002t0005g0040a0001c0002t0005g0041 | 2 | HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.1520+5588A>G | DLG3 | ENSG00000082458.12 | transcript | ENST00000374360.8 | protein_coding | 10/18 | chrX | 70484852 | ||||||
| chrX:70484934
|
C | T | 1 | a0001c0001t0001g0026 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1520+5670C>T | DLG3 | ENSG00000082458.12 | transcript | ENST00000374360.8 | protein_coding | 10/18 | chrX | 70484934 | ||||||
| chrX:70484947
|
G | A | 1 | a0001c0001t0002g0072 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.1520+5683G>A | DLG3 | ENSG00000082458.12 | transcript | ENST00000374360.8 | protein_coding | 10/18 | chrX | 70484947 | ||||||
| chrX:70485043
|
T | C | 1 | a0001c0001t0002g0054 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.1520+5779T>C | DLG3 | ENSG00000082458.12 | transcript | ENST00000374360.8 | protein_coding | 10/18 | chrX | 70485043 | ||||||
| chrX:70485196
|
C | A | 1 | a0001c0001t0001g0152 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.1520+5932C>A | DLG3 | ENSG00000082458.12 | transcript | ENST00000374360.8 | protein_coding | 10/18 | chrX | 70485196 | ||||||
| chrX:70485805
|
G | C | 1 | a0001c0001t0001g0171 | 1 | NA18993.hp2 | intron_variant | MODIFIER | c.1521-6302G>C | DLG3 | ENSG00000082458.12 | transcript | ENST00000374360.8 | protein_coding | 10/18 | chrX | 70485805 | ||||||
| chrX:70485919
|
C | T | 1 | a0001c0001t0001g0177 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.1521-6188C>T | DLG3 | ENSG00000082458.12 | transcript | ENST00000374360.8 | protein_coding | 10/18 | chrX | 70485919 | ||||||
| chrX:70486020
|
G | C | 1 | a0001c0001t0001g0208 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1521-6087G>C | DLG3 | ENSG00000082458.12 | transcript | ENST00000374360.8 | protein_coding | 10/18 | chrX | 70486020 | ||||||
| chrX:70486169
|
T | G | 3 | a0001c0001t0001g0017a0001c0001t0001g0239a0001c0001t0029g0238 | 4 | HG02257.hp1 HG02451.hp2 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.1521-5938T>G | DLG3 | ENSG00000082458.12 | transcript | ENST00000374360.8 | protein_coding | 10/18 | chrX | 70486169 | ||||||
| chrX:70486184
|
G | T | 148 | a0001c0001t0001g0015a0001c0001t0001g0016a0001c0001t0001g0017others(145): Show | 156 | HG00099.hp1 HG00621.hp1 HG00642.hp1 others(153): Show |
intron_variant | MODIFIER | c.1521-5923G>T | DLG3 | ENSG00000082458.12 | transcript | ENST00000374360.8 | protein_coding | 10/18 | chrX | 70486184 | ||||||
| chrX:70486371
|
A | G | 1 | a0001c0001t0001g0204 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.1521-5736A>G | DLG3 | ENSG00000082458.12 | transcript | ENST00000374360.8 | protein_coding | 10/18 | chrX | 70486371 | ||||||
| chrX:70486455
|
A | C | 91 | a0001c0001t0001g0015a0001c0001t0001g0016a0001c0001t0001g0017others(88): Show | 98 | HG00621.hp1 HG00733.hp1 HG00735.hp1 others(95): Show |
intron_variant | MODIFIER | c.1521-5652A>C | DLG3 | ENSG00000082458.12 | transcript | ENST00000374360.8 | protein_coding | 10/18 | chrX | 70486455 | ||||||
| chrX:70486579
|
C | T | 1 | a0001c0001t0001g0026 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1521-5528C>T | DLG3 | ENSG00000082458.12 | transcript | ENST00000374360.8 | protein_coding | 10/18 | chrX | 70486579 | ||||||
| chrX:70486609
|
T | C | 1 | a0001c0001t0002g0080 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.1521-5498T>C | DLG3 | ENSG00000082458.12 | transcript | ENST00000374360.8 | protein_coding | 10/18 | chrX | 70486609 | ||||||
| chrX:70486650
|
C | CT | 72 | a0001c0001t0001g0015a0001c0001t0001g0016a0001c0001t0001g0023others(69): Show | 78 | HG00733.hp1 HG00738.hp1 HG01081.hp2 others(75): Show |
intron_variant | MODIFIER | c.1521-5438dupT | DLG3 | ENSG00000082458.12 | transcript | ENST00000374360.8 | protein_coding | 10/18 | INFO_REALIGN_3_PRIME | chrX | 70486650 | |||||
| chrX:70486650
|
C | CTT | 4 | a0001c0001t0001g0045a0001c0001t0001g0048a0001c0001t0001g0173others(1): Show | 4 | HG01255.hp1 HG02451.hp1 HG02572.hp1 others(1): Show |
intron_variant | MODIFIER | c.1521-5439_1521-543 others(6): Show |
DLG3 | ENSG00000082458.12 | transcript | ENST00000374360.8 | protein_coding | 10/18 | INFO_REALIGN_3_PRIME | chrX | 70486650 | |||||
| chrX:70486650
|
CT | C | 4 | a0001c0001t0001g0249a0001c0001t0004g0119a0001c0001t0004g0233others(1): Show | 4 | HG02922.hp1 NA18906.hp1 NA18968.hp1 others(1): Show |
intron_variant | MODIFIER | c.1521-5438delT | DLG3 | ENSG00000082458.12 | transcript | ENST00000374360.8 | protein_coding | 10/18 | INFO_REALIGN_3_PRIME | chrX | 70486650 | |||||
| chrX:70486668
|
T | TTTC | 3 | a0001c0001t0001g0137a0001c0001t0001g0235a0001c0001t0001g0236 | 3 | HG03453.hp2 HG03471.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.1521-5438_1521-543 others(7): Show |
DLG3 | ENSG00000082458.12 | transcript | ENST00000374360.8 | protein_coding | 10/18 | INFO_REALIGN_3_PRIME | chrX | 70486668 | |||||
| chrX:70486669
|
T | TC | 1 | a0001c0001t0001g0026 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1521-5437dupC | DLG3 | ENSG00000082458.12 | transcript | ENST00000374360.8 | protein_coding | 10/18 | INFO_REALIGN_3_PRIME | chrX | 70486669 | |||||
| chrX:70486669
|
T | TTC | 14 | a0001c0001t0001g0029a0001c0001t0001g0038a0001c0001t0001g0204others(11): Show | 15 | HG00099.hp1 HG00642.hp1 HG00733.hp2 others(12): Show |
intron_variant | MODIFIER | c.1521-5438_1521-543 others(6): Show |
DLG3 | ENSG00000082458.12 | transcript | ENST00000374360.8 | protein_coding | 10/18 | chrX | 70486669 | ||||||
| chrX:70486746
|
C | T | 1 | a0001c0001t0025g0139 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.1521-5361C>T | DLG3 | ENSG00000082458.12 | transcript | ENST00000374360.8 | protein_coding | 10/18 | chrX | 70486746 | ||||||
| chrX:70486825
|
A | G | 1 | a0001c0001t0027g0051 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.1521-5282A>G | DLG3 | ENSG00000082458.12 | transcript | ENST00000374360.8 | protein_coding | 10/18 | chrX | 70486825 | ||||||
| chrX:70486840
|
A | C | 1 | a0001c0001t0001g0216 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.1521-5267A>C | DLG3 | ENSG00000082458.12 | transcript | ENST00000374360.8 | protein_coding | 10/18 | chrX | 70486840 | ||||||
| chrX:70487064
|
T | G | 1 | a0001c0001t0001g0194 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.1521-5043T>G | DLG3 | ENSG00000082458.12 | transcript | ENST00000374360.8 | protein_coding | 10/18 | chrX | 70487064 | ||||||
| chrX:70487089
|
C | T | 6 | a0001c0002t0005g0039a0001c0002t0005g0040a0001c0002t0005g0041others(3): Show | 6 | HG01167.hp1 HG01169.hp1 HG02486.hp1 others(3): Show |
intron_variant | MODIFIER | c.1521-5018C>T | DLG3 | ENSG00000082458.12 | transcript | ENST00000374360.8 | protein_coding | 10/18 | chrX | 70487089 | ||||||
| chrX:70487166
|
G | T | 149 | a0001c0001t0001g0015a0001c0001t0001g0016a0001c0001t0001g0017others(146): Show | 157 | HG00099.hp1 HG00621.hp1 HG00642.hp1 others(154): Show |
intron_variant | MODIFIER | c.1521-4941G>T | DLG3 | ENSG00000082458.12 | transcript | ENST00000374360.8 | protein_coding | 10/18 | chrX | 70487166 | ||||||
| chrX:70487313
|
C | T | 1 | a0001c0001t0001g0026 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1521-4794C>T | DLG3 | ENSG00000082458.12 | transcript | ENST00000374360.8 | protein_coding | 10/18 | chrX | 70487313 | ||||||
| chrX:70487526
|
CT | C | 1 | a0001c0001t0002g0090 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.1521-4577delT | DLG3 | ENSG00000082458.12 | transcript | ENST00000374360.8 | protein_coding | 10/18 | INFO_REALIGN_3_PRIME | chrX | 70487526 | |||||
| chrX:70487535
|
T | C | 16 | a0001c0001t0001g0044a0001c0001t0001g0045a0001c0001t0001g0046others(13): Show | 16 | HG01255.hp1 HG02280.hp2 HG02451.hp1 others(13): Show |
intron_variant | MODIFIER | c.1521-4572T>C | DLG3 | ENSG00000082458.12 | transcript | ENST00000374360.8 | protein_coding | 10/18 | chrX | 70487535 | ||||||
| chrX:70487642
|
A | G | 247 | a0001c0001t0001g0015a0001c0001t0001g0016a0001c0001t0001g0017others(244): Show | 272 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(269): Show |
intron_variant | MODIFIER | c.1521-4465A>G | DLG3 | ENSG00000082458.12 | transcript | ENST00000374360.8 | protein_coding | 10/18 | chrX | 70487642 | ||||||
| chrX:70487713
|
G | A | 1 | a0001c0001t0001g0182 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.1521-4394G>A | DLG3 | ENSG00000082458.12 | transcript | ENST00000374360.8 | protein_coding | 10/18 | chrX | 70487713 | ||||||
| chrX:70487871
|
G | T | 1 | a0001c0001t0016g0066 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.1521-4236G>T | DLG3 | ENSG00000082458.12 | transcript | ENST00000374360.8 | protein_coding | 10/18 | chrX | 70487871 | ||||||
| chrX:70487948
|
A | T | 1 | a0001c0001t0001g0046 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.1521-4159A>T | DLG3 | ENSG00000082458.12 | transcript | ENST00000374360.8 | protein_coding | 10/18 | chrX | 70487948 | ||||||
| chrX:70488305
|
C | T | 1 | a0001c0001t0001g0026 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1521-3802C>T | DLG3 | ENSG00000082458.12 | transcript | ENST00000374360.8 | protein_coding | 10/18 | chrX | 70488305 | ||||||
| chrX:70488373
|
G | A | 3 | a0001c0001t0002g0060a0001c0001t0002g0067a0001c0001t0006g0109 | 3 | HG00735.hp2 HG01346.hp2 HG03669.hp2 |
intron_variant | MODIFIER | c.1521-3734G>A | DLG3 | ENSG00000082458.12 | transcript | ENST00000374360.8 | protein_coding | 10/18 | chrX | 70488373 | ||||||
| chrX:70488420
|
G | A | 1 | a0001c0001t0001g0216 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.1521-3687G>A | DLG3 | ENSG00000082458.12 | transcript | ENST00000374360.8 | protein_coding | 10/18 | chrX | 70488420 | ||||||
| chrX:70488485
|
C | T | 3 | a0001c0001t0002g0062a0001c0001t0006g0061a0001c0001t0008g0063 | 3 | NA18942.hp1 NA19011.hp2 NA20905.hp1 |
intron_variant | MODIFIER | c.1521-3622C>T | DLG3 | ENSG00000082458.12 | transcript | ENST00000374360.8 | protein_coding | 10/18 | chrX | 70488485 | ||||||
| chrX:70488600
|
A | T | 149 | a0001c0001t0001g0015a0001c0001t0001g0016a0001c0001t0001g0017others(146): Show | 157 | HG00099.hp1 HG00621.hp1 HG00642.hp1 others(154): Show |
intron_variant | MODIFIER | c.1521-3507A>T | DLG3 | ENSG00000082458.12 | transcript | ENST00000374360.8 | protein_coding | 10/18 | chrX | 70488600 | ||||||
| chrX:70488734
|
G | A | 1 | a0001c0001t0002g0078 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.1521-3373G>A | DLG3 | ENSG00000082458.12 | transcript | ENST00000374360.8 | protein_coding | 10/18 | chrX | 70488734 | ||||||
| chrX:70488957
|
C | T | 1 | a0007c0004t0002g0131 | 1 | NA18972.hp2 | intron_variant | MODIFIER | c.1521-3150C>T | DLG3 | ENSG00000082458.12 | transcript | ENST00000374360.8 | protein_coding | 10/18 | chrX | 70488957 | ||||||
| chrX:70489119
|
G | A | 150 | a0001c0001t0001g0015a0001c0001t0001g0016a0001c0001t0001g0017others(147): Show | 158 | HG00099.hp1 HG00621.hp1 HG00642.hp1 others(155): Show |
intron_variant | MODIFIER | c.1521-2988G>A | DLG3 | ENSG00000082458.12 | transcript | ENST00000374360.8 | protein_coding | 10/18 | chrX | 70489119 | ||||||
| chrX:70489282
|
A | AT | 3 | a0001c0001t0001g0044a0001c0001t0001g0228a0001c0001t0001g0229 | 3 | HG02896.hp2 HG02897.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.1521-2816dupT | DLG3 | ENSG00000082458.12 | transcript | ENST00000374360.8 | protein_coding | 10/18 | INFO_REALIGN_3_PRIME | chrX | 70489282 | |||||
| chrX:70489282
|
AT | A | 1 | a0001c0001t0001g0205 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.1521-2816delT | DLG3 | ENSG00000082458.12 | transcript | ENST00000374360.8 | protein_coding | 10/18 | INFO_REALIGN_3_PRIME | chrX | 70489282 | |||||
| chrX:70489391
|
C | A | 1 | a0001c0001t0020g0218 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.1521-2716C>A | DLG3 | ENSG00000082458.12 | transcript | ENST00000374360.8 | protein_coding | 10/18 | chrX | 70489391 | ||||||
| chrX:70489549
|
C | T | 1 | a0001c0001t0002g0093 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.1521-2558C>T | DLG3 | ENSG00000082458.12 | transcript | ENST00000374360.8 | protein_coding | 10/18 | chrX | 70489549 | ||||||
| chrX:70489580
|
G | A | 9 | a0001c0001t0001g0044a0001c0001t0001g0045a0001c0001t0001g0046others(6): Show | 9 | HG02280.hp2 HG02451.hp1 HG02559.hp1 others(6): Show |
intron_variant | MODIFIER | c.1521-2527G>A | DLG3 | ENSG00000082458.12 | transcript | ENST00000374360.8 | protein_coding | 10/18 | chrX | 70489580 | ||||||
| chrX:70489695
|
G | A | 1 | a0001c0001t0002g0220 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.1521-2412G>A | DLG3 | ENSG00000082458.12 | transcript | ENST00000374360.8 | protein_coding | 10/18 | chrX | 70489695 | ||||||
| chrX:70489923
|
C | T | 1 | a0001c0001t0001g0226 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1521-2184C>T | DLG3 | ENSG00000082458.12 | transcript | ENST00000374360.8 | protein_coding | 10/18 | chrX | 70489923 | ||||||
| chrX:70489967
|
A | G | 1 | a0001c0001t0001g0216 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.1521-2140A>G | DLG3 | ENSG00000082458.12 | transcript | ENST00000374360.8 | protein_coding | 10/18 | chrX | 70489967 | ||||||
| chrX:70490051
|
C | T | 6 | a0001c0002t0005g0039a0001c0002t0005g0040a0001c0002t0005g0041others(3): Show | 6 | HG01167.hp1 HG01169.hp1 HG02486.hp1 others(3): Show |
intron_variant | MODIFIER | c.1521-2056C>T | DLG3 | ENSG00000082458.12 | transcript | ENST00000374360.8 | protein_coding | 10/18 | chrX | 70490051 | ||||||
| chrX:70490310
|
G | A | 1 | a0001c0001t0008g0073 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.1521-1797G>A | DLG3 | ENSG00000082458.12 | transcript | ENST00000374360.8 | protein_coding | 10/18 | chrX | 70490310 | ||||||
| chrX:70490410
|
TTC | T | 1 | a0001c0001t0001g0026 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1521-1695_1521-169 others(6): Show |
DLG3 | ENSG00000082458.12 | transcript | ENST00000374360.8 | protein_coding | 10/18 | INFO_REALIGN_3_PRIME | chrX | 70490410 | |||||
| chrX:70490436
|
C | T | 6 | a0001c0002t0005g0039a0001c0002t0005g0040a0001c0002t0005g0041others(3): Show | 6 | HG01167.hp1 HG01169.hp1 HG02486.hp1 others(3): Show |
intron_variant | MODIFIER | c.1521-1671C>T | DLG3 | ENSG00000082458.12 | transcript | ENST00000374360.8 | protein_coding | 10/18 | chrX | 70490436 | ||||||
| chrX:70490907
|
CT | C | 1 | a0001c0001t0001g0229 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.1521-1191delT | DLG3 | ENSG00000082458.12 | transcript | ENST00000374360.8 | protein_coding | 10/18 | INFO_REALIGN_3_PRIME | chrX | 70490907 | |||||
| chrX:70490919
|
C | CT | 7 | a0001c0001t0001g0146a0001c0002t0005g0039a0001c0002t0005g0040others(4): Show | 7 | HG01167.hp1 HG01169.hp1 HG02486.hp1 others(4): Show |
intron_variant | MODIFIER | c.1521-1177dupT | DLG3 | ENSG00000082458.12 | transcript | ENST00000374360.8 | protein_coding | 10/18 | INFO_REALIGN_3_PRIME | chrX | 70490919 | |||||
| chrX:70490952
|
G | A | 1 | a0001c0001t0001g0231 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.1521-1155G>A | DLG3 | ENSG00000082458.12 | transcript | ENST00000374360.8 | protein_coding | 10/18 | chrX | 70490952 | ||||||
| chrX:70490973
|
C | T | 10 | a0001c0001t0003g0008a0001c0001t0003g0028a0001c0001t0003g0030others(7): Show | 11 | HG00099.hp1 HG00642.hp1 HG00733.hp2 others(8): Show |
intron_variant | MODIFIER | c.1521-1134C>T | DLG3 | ENSG00000082458.12 | transcript | ENST00000374360.8 | protein_coding | 10/18 | chrX | 70490973 | ||||||
| chrX:70491074
|
A | G | 152 | a0001c0001t0001g0015a0001c0001t0001g0016a0001c0001t0001g0017others(149): Show | 160 | HG00099.hp1 HG00621.hp1 HG00642.hp1 others(157): Show |
intron_variant | MODIFIER | c.1521-1033A>G | DLG3 | ENSG00000082458.12 | transcript | ENST00000374360.8 | protein_coding | 10/18 | chrX | 70491074 | ||||||
| chrX:70491430
|
A | G | 2 | a0001c0001t0001g0016a0001c0001t0001g0160 | 3 | NA18944.hp1 NA18946.hp2 NA19004.hp1 |
intron_variant | MODIFIER | c.1521-677A>G | DLG3 | ENSG00000082458.12 | transcript | ENST00000374360.8 | protein_coding | 10/18 | chrX | 70491430 | ||||||
| chrX:70491632
|
G | A | 1 | a0001c0001t0005g0037 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.1521-475G>A | DLG3 | ENSG00000082458.12 | transcript | ENST00000374360.8 | protein_coding | 10/18 | chrX | 70491632 | ||||||
| chrX:70491689
|
G | A | 23 | a0001c0001t0001g0019a0001c0001t0001g0058a0001c0001t0001g0059others(20): Show | 23 | HG00621.hp1 HG02015.hp1 HG02155.hp2 others(20): Show |
intron_variant | MODIFIER | c.1521-418G>A | DLG3 | ENSG00000082458.12 | transcript | ENST00000374360.8 | protein_coding | 10/18 | chrX | 70491689 | ||||||
| chrX:70491830
|
G | C | 6 | a0001c0001t0001g0021a0001c0001t0001g0224a0001c0001t0001g0225others(3): Show | 6 | HG01884.hp1 HG02109.hp2 HG02145.hp1 others(3): Show |
intron_variant | MODIFIER | c.1521-277G>C | DLG3 | ENSG00000082458.12 | transcript | ENST00000374360.8 | protein_coding | 10/18 | chrX | 70491830 | ||||||
| chrX:70492054
|
T | C | 1 | a0001c0001t0002g0126 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.1521-53T>C | DLG3 | ENSG00000082458.12 | transcript | ENST00000374360.8 | protein_coding | 10/18 | chrX | 70492054 | ||||||
| chrX:70492405
|
G | A | 1 | a0001c0001t0019g0141 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1698-116G>A | DLG3 | ENSG00000082458.12 | transcript | ENST00000374360.8 | protein_coding | 11/18 | chrX | 70492405 | ||||||
| chrX:70492723
|
T | C | 1 | a0001c0001t0002g0105 | 1 | HG01169.hp2 | intron_variant | MODIFIER | c.1773+127T>C | DLG3 | ENSG00000082458.12 | transcript | ENST00000374360.8 | protein_coding | 12/18 | chrX | 70492723 | ||||||
| chrX:70492893
|
T | C | 2 | a0001c0001t0001g0149a0001c0001t0001g0151 | 2 | NA19002.hp2 NA19011.hp1 |
intron_variant | MODIFIER | c.1773+297T>C | DLG3 | ENSG00000082458.12 | transcript | ENST00000374360.8 | protein_coding | 12/18 | chrX | 70492893 | ||||||
| chrX:70493570
|
C | T | 7 | a0001c0001t0001g0044a0001c0001t0001g0045a0001c0001t0001g0046others(4): Show | 7 | HG02280.hp2 HG02451.hp1 HG02559.hp1 others(4): Show |
intron_variant | MODIFIER | c.1773+974C>T | DLG3 | ENSG00000082458.12 | transcript | ENST00000374360.8 | protein_coding | 12/18 | chrX | 70493570 | ||||||
| chrX:70493737
|
A | T | 1 | a0001c0001t0011g0043 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.1773+1141A>T | DLG3 | ENSG00000082458.12 | transcript | ENST00000374360.8 | protein_coding | 12/18 | chrX | 70493737 | ||||||
| chrX:70494138
|
T | C | 2 | a0001c0001t0001g0026a0001c0001t0022g0227 | 2 | HG02886.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.1774-1270T>C | DLG3 | ENSG00000082458.12 | transcript | ENST00000374360.8 | protein_coding | 12/18 | chrX | 70494138 | ||||||
| chrX:70494419
|
T | A | 1 | a0001c0001t0001g0204 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.1774-989T>A | DLG3 | ENSG00000082458.12 | transcript | ENST00000374360.8 | protein_coding | 12/18 | chrX | 70494419 | ||||||
| chrX:70494495
|
T | C | 17 | a0001c0001t0001g0026a0001c0001t0001g0133a0001c0001t0001g0140others(14): Show | 19 | HG00733.hp1 HG01070.hp2 HG01106.hp1 others(16): Show |
intron_variant | MODIFIER | c.1774-913T>C | DLG3 | ENSG00000082458.12 | transcript | ENST00000374360.8 | protein_coding | 12/18 | chrX | 70494495 | ||||||
| chrX:70494634
|
A | G | 12 | a0001c0001t0001g0038a0001c0001t0003g0008a0001c0001t0003g0028others(9): Show | 13 | HG00099.hp1 HG00642.hp1 HG00733.hp2 others(10): Show |
intron_variant | MODIFIER | c.1774-774A>G | DLG3 | ENSG00000082458.12 | transcript | ENST00000374360.8 | protein_coding | 12/18 | chrX | 70494634 | ||||||
| chrX:70494662
|
C | T | 1 | a0001c0001t0002g0132 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.1774-746C>T | DLG3 | ENSG00000082458.12 | transcript | ENST00000374360.8 | protein_coding | 12/18 | chrX | 70494662 | ||||||
| chrX:70494715
|
T | C | 1 | a0001c0001t0024g0052 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.1774-693T>C | DLG3 | ENSG00000082458.12 | transcript | ENST00000374360.8 | protein_coding | 12/18 | chrX | 70494715 | ||||||
| chrX:70494942
|
C | T | 6 | a0001c0002t0005g0039a0001c0002t0005g0040a0001c0002t0005g0041others(3): Show | 6 | HG01167.hp1 HG01169.hp1 HG02486.hp1 others(3): Show |
intron_variant | MODIFIER | c.1774-466C>T | DLG3 | ENSG00000082458.12 | transcript | ENST00000374360.8 | protein_coding | 12/18 | chrX | 70494942 | ||||||
| chrX:70494951
|
G | T | 4 | a0001c0001t0001g0209a0001c0001t0001g0213a0001c0001t0001g0240others(1): Show | 4 | HG01891.hp2 HG02559.hp2 HG02809.hp1 others(1): Show |
intron_variant | MODIFIER | c.1774-457G>T | DLG3 | ENSG00000082458.12 | transcript | ENST00000374360.8 | protein_coding | 12/18 | chrX | 70494951 | ||||||
| chrX:70495312
|
C | G | 6 | a0001c0002t0005g0039a0001c0002t0005g0040a0001c0002t0005g0041others(3): Show | 6 | HG01167.hp1 HG01169.hp1 HG02486.hp1 others(3): Show |
intron_variant | MODIFIER | c.1774-96C>G | DLG3 | ENSG00000082458.12 | transcript | ENST00000374360.8 | protein_coding | 12/18 | chrX | 70495312 | ||||||
| chrX:70495945
|
G | A | 1 | a0001c0001t0001g0159 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.1819+492G>A | DLG3 | ENSG00000082458.12 | transcript | ENST00000374360.8 | protein_coding | 13/18 | chrX | 70495945 | ||||||
| chrX:70496042
|
A | G | 1 | a0005c0008t0002g0129 | 1 | NA18988.hp1 | intron_variant | MODIFIER | c.1819+589A>G | DLG3 | ENSG00000082458.12 | transcript | ENST00000374360.8 | protein_coding | 13/18 | chrX | 70496042 | ||||||
| chrX:70496127
|
G | A | 12 | a0001c0001t0001g0023a0001c0001t0001g0024a0001c0001t0001g0145others(9): Show | 12 | HG01261.hp1 HG01361.hp1 HG03831.hp2 others(9): Show |
intron_variant | MODIFIER | c.1819+674G>A | DLG3 | ENSG00000082458.12 | transcript | ENST00000374360.8 | protein_coding | 13/18 | chrX | 70496127 | ||||||
| chrX:70496264
|
C | G | 1 | a0001c0001t0001g0046 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.1819+811C>G | DLG3 | ENSG00000082458.12 | transcript | ENST00000374360.8 | protein_coding | 13/18 | chrX | 70496264 | ||||||
| chrX:70496596
|
G | A | 1 | a0001c0001t0005g0037 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.1819+1143G>A | DLG3 | ENSG00000082458.12 | transcript | ENST00000374360.8 | protein_coding | 13/18 | chrX | 70496596 | ||||||
| chrX:70496687
|
C | T | 6 | a0001c0002t0005g0039a0001c0002t0005g0040a0001c0002t0005g0041others(3): Show | 6 | HG01167.hp1 HG01169.hp1 HG02486.hp1 others(3): Show |
intron_variant | MODIFIER | c.1819+1234C>T | DLG3 | ENSG00000082458.12 | transcript | ENST00000374360.8 | protein_coding | 13/18 | chrX | 70496687 | ||||||
| chrX:70496717
|
C | T | 6 | a0001c0002t0005g0039a0001c0002t0005g0040a0001c0002t0005g0041others(3): Show | 6 | HG01167.hp1 HG01169.hp1 HG02486.hp1 others(3): Show |
intron_variant | MODIFIER | c.1819+1264C>T | DLG3 | ENSG00000082458.12 | transcript | ENST00000374360.8 | protein_coding | 13/18 | chrX | 70496717 | ||||||
| chrX:70496877
|
G | C | 100 | a0001c0001t0001g0015a0001c0001t0001g0016a0001c0001t0001g0017others(97): Show | 105 | HG00280.hp1 HG00621.hp1 HG00735.hp1 others(102): Show |
intron_variant | MODIFIER | c.1819+1424G>C | DLG3 | ENSG00000082458.12 | transcript | ENST00000374360.8 | protein_coding | 13/18 | chrX | 70496877 | ||||||
| chrX:70496898
|
A | AATTTG | 1 | a0001c0001t0006g0124 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.1819+1449_1819+145 others(9): Show |
DLG3 | ENSG00000082458.12 | transcript | ENST00000374360.8 | protein_coding | 13/18 | INFO_REALIGN_3_PRIME | chrX | 70496898 | |||||
| chrX:70497951
|
C | A | 2 | a0001c0001t0002g0071a0001c0001t0002g0072 | 2 | NA18962.hp1 NA19077.hp2 |
intron_variant | MODIFIER | c.1820-569C>A | DLG3 | ENSG00000082458.12 | transcript | ENST00000374360.8 | protein_coding | 13/18 | chrX | 70497951 | ||||||
| chrX:70497965
|
G | C | 18 | a0001c0001t0001g0022a0001c0001t0001g0026a0001c0001t0001g0133others(15): Show | 20 | HG00733.hp1 HG01070.hp2 HG01106.hp1 others(17): Show |
intron_variant | MODIFIER | c.1820-555G>C | DLG3 | ENSG00000082458.12 | transcript | ENST00000374360.8 | protein_coding | 13/18 | chrX | 70497965 | ||||||
| chrX:70498218
|
G | A | 2 | a0001c0001t0024g0052a0001c0001t0027g0051 | 2 | HG01081.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.1820-302G>A | DLG3 | ENSG00000082458.12 | transcript | ENST00000374360.8 | protein_coding | 13/18 | chrX | 70498218 | ||||||
| chrX:70498262
|
T | TG | 1 | a0001c0001t0006g0124 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.1820-254dupG | DLG3 | ENSG00000082458.12 | transcript | ENST00000374360.8 | protein_coding | 13/18 | INFO_REALIGN_3_PRIME | chrX | 70498262 | |||||
| chrX:70498464
|
C | T | 148 | a0001c0001t0001g0015a0001c0001t0001g0016a0001c0001t0001g0017others(145): Show | 156 | HG00099.hp1 HG00621.hp1 HG00642.hp1 others(153): Show |
intron_variant | MODIFIER | c.1820-56C>T | DLG3 | ENSG00000082458.12 | transcript | ENST00000374360.8 | protein_coding | 13/18 | chrX | 70498464 | ||||||
| chrX:70498590
|
CT | C | 1 | a0001c0001t0006g0124 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.1870+22delT | DLG3 | ENSG00000082458.12 | transcript | ENST00000374360.8 | protein_coding | 14/18 | INFO_REALIGN_3_PRIME | chrX | 70498590 | |||||
| chrX:70498597
|
T | C | 2 | a0001c0001t0002g0067a0001c0001t0006g0109 | 2 | HG00735.hp2 HG03669.hp2 |
intron_variant | MODIFIER | c.1870+27T>C | DLG3 | ENSG00000082458.12 | transcript | ENST00000374360.8 | protein_coding | 14/18 | chrX | 70498597 | ||||||
| chrX:70498616
|
G | A | 6 | a0001c0002t0005g0039a0001c0002t0005g0040a0001c0002t0005g0041others(3): Show | 6 | HG01167.hp1 HG01169.hp1 HG02486.hp1 others(3): Show |
intron_variant | MODIFIER | c.1870+46G>A | DLG3 | ENSG00000082458.12 | transcript | ENST00000374360.8 | protein_coding | 14/18 | chrX | 70498616 | ||||||
| chrX:70498636
|
T | TG | 1 | a0001c0001t0006g0124 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.1870+68dupG | DLG3 | ENSG00000082458.12 | transcript | ENST00000374360.8 | protein_coding | 14/18 | INFO_REALIGN_3_PRIME | chrX | 70498636 | |||||
| chrX:70498640
|
T | TG | 1 | a0001c0001t0006g0124 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.1870+71dupG | DLG3 | ENSG00000082458.12 | transcript | ENST00000374360.8 | protein_coding | 14/18 | INFO_REALIGN_3_PRIME | chrX | 70498640 | |||||
| chrX:70498683
|
CTCAT | C | 148 | a0001c0001t0001g0015a0001c0001t0001g0016a0001c0001t0001g0017others(145): Show | 156 | HG00099.hp1 HG00621.hp1 HG00642.hp1 others(153): Show |
intron_variant | MODIFIER | c.1870+114_1870+117d others(6): Show |
DLG3 | ENSG00000082458.12 | transcript | ENST00000374360.8 | protein_coding | 14/18 | chrX | 70498683 | ||||||
| chrX:70498703
|
TG | T | 1 | a0001c0001t0006g0124 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.1870+136delG | DLG3 | ENSG00000082458.12 | transcript | ENST00000374360.8 | protein_coding | 14/18 | INFO_REALIGN_3_PRIME | chrX | 70498703 | |||||
| chrX:70498848
|
G | A | 1 | a0001c0001t0025g0139 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.1870+278G>A | DLG3 | ENSG00000082458.12 | transcript | ENST00000374360.8 | protein_coding | 14/18 | chrX | 70498848 | ||||||
| chrX:70499009
|
T | G | 1 | a0001c0001t0001g0171 | 1 | NA18993.hp2 | intron_variant | MODIFIER | c.1871-167T>G | DLG3 | ENSG00000082458.12 | transcript | ENST00000374360.8 | protein_coding | 14/18 | chrX | 70499009 | ||||||
| chrX:70499342
|
T | G | 1 | a0001c0001t0003g0034 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.1972+65T>G | DLG3 | ENSG00000082458.12 | transcript | ENST00000374360.8 | protein_coding | 15/18 | chrX | 70499342 | ||||||
| chrX:70499354
|
T | C | 1 | a0001c0001t0001g0204 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.1972+77T>C | DLG3 | ENSG00000082458.12 | transcript | ENST00000374360.8 | protein_coding | 15/18 | chrX | 70499354 | ||||||
| chrX:70499604
|
G | C | 1 | a0001c0001t0002g0100 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.1973-273G>C | DLG3 | ENSG00000082458.12 | transcript | ENST00000374360.8 | protein_coding | 15/18 | chrX | 70499604 | ||||||
| chrX:70499725
|
C | T | 148 | a0001c0001t0001g0015a0001c0001t0001g0016a0001c0001t0001g0017others(145): Show | 156 | HG00099.hp1 HG00621.hp1 HG00642.hp1 others(153): Show |
intron_variant | MODIFIER | c.1973-152C>T | DLG3 | ENSG00000082458.12 | transcript | ENST00000374360.8 | protein_coding | 15/18 | chrX | 70499725 | ||||||
| chrX:70499759
|
G | GA | 3 | a0001c0001t0001g0029a0001c0001t0001g0147a0001c0001t0006g0143 | 3 | HG02280.hp1 HG04115.hp1 HG04204.hp1 |
intron_variant | MODIFIER | c.1973-108dupA | DLG3 | ENSG00000082458.12 | transcript | ENST00000374360.8 | protein_coding | 15/18 | INFO_REALIGN_3_PRIME | chrX | 70499759 | |||||
| chrX:70500075
|
A | AG | 1 | a0001c0001t0001g0201 | 1 | NA18991.hp2 | intron_variant | MODIFIER | c.2145+30dupG | DLG3 | ENSG00000082458.12 | transcript | ENST00000374360.8 | protein_coding | 16/18 | INFO_REALIGN_3_PRIME | chrX | 70500075 | |||||
| chrX:70500247
|
A | C | 1 | a0001c0001t0001g0215 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.2145+198A>C | DLG3 | ENSG00000082458.12 | transcript | ENST00000374360.8 | protein_coding | 16/18 | chrX | 70500247 | ||||||
| chrX:70500322
|
C | G | 10 | a0001c0001t0003g0008a0001c0001t0003g0028a0001c0001t0003g0030others(7): Show | 11 | HG00099.hp1 HG00642.hp1 HG00733.hp2 others(8): Show |
intron_variant | MODIFIER | c.2146-149C>G | DLG3 | ENSG00000082458.12 | transcript | ENST00000374360.8 | protein_coding | 16/18 | chrX | 70500322 | ||||||
| chrX:70500352
|
C | T | 1 | a0001c0001t0001g0171 | 1 | NA18993.hp2 | intron_variant | MODIFIER | c.2146-119C>T | DLG3 | ENSG00000082458.12 | transcript | ENST00000374360.8 | protein_coding | 16/18 | chrX | 70500352 | ||||||
| chrX:70500353
|
G | C | 1 | a0001c0001t0001g0140 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.2146-118G>C | DLG3 | ENSG00000082458.12 | transcript | ENST00000374360.8 | protein_coding | 16/18 | chrX | 70500353 | ||||||
| chrX:70500367
|
A | AC | 1 | a0001c0001t0001g0201 | 1 | NA18991.hp2 | intron_variant | MODIFIER | c.2146-99dupC | DLG3 | ENSG00000082458.12 | transcript | ENST00000374360.8 | protein_coding | 16/18 | INFO_REALIGN_3_PRIME | chrX | 70500367 | |||||
| chrX:70500622
|
C | T | 1 | a0001c0001t0011g0043 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.2255+42C>T | DLG3 | ENSG00000082458.12 | transcript | ENST00000374360.8 | protein_coding | 17/18 | chrX | 70500622 | ||||||
| chrX:70500670
|
T | G | 6 | a0001c0002t0005g0039a0001c0002t0005g0040a0001c0002t0005g0041others(3): Show | 6 | HG01167.hp1 HG01169.hp1 HG02486.hp1 others(3): Show |
intron_variant | MODIFIER | c.2255+90T>G | DLG3 | ENSG00000082458.12 | transcript | ENST00000374360.8 | protein_coding | 17/18 | chrX | 70500670 | ||||||
| chrX:70500757
|
G | A | 1 | a0001c0001t0002g0092 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.2256-141G>A | DLG3 | ENSG00000082458.12 | transcript | ENST00000374360.8 | protein_coding | 17/18 | chrX | 70500757 | ||||||
| chrX:70500840
|
T | C | 1 | a0001c0001t0001g0226 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.2256-58T>C | DLG3 | ENSG00000082458.12 | transcript | ENST00000374360.8 | protein_coding | 17/18 | chrX | 70500840 | ||||||
| chrX:70500866
|
G | T | 1 | a0001c0001t0002g0064 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.2256-32G>T | DLG3 | ENSG00000082458.12 | transcript | ENST00000374360.8 | protein_coding | 17/18 | chrX | 70500866 | ||||||
| chrX:70501038
|
C | T | 1 | a0001c0001t0001g0199 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.2347+49C>T | DLG3 | ENSG00000082458.12 | transcript | ENST00000374360.8 | protein_coding | 18/18 | chrX | 70501038 | ||||||
| chrX:70501409
|
C | CTGTG | 1 | a0001c0001t0002g0170 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.2347+423_2347+424i others(6): Show |
DLG3 | ENSG00000082458.12 | transcript | ENST00000374360.8 | protein_coding | 18/18 | INFO_REALIGN_3_PRIME | chrX | 70501409 | |||||
| chrX:70501409
|
C | CTGTGTGT others(1): Show |
8 | a0001c0001t0001g0019a0001c0001t0001g0021a0001c0001t0001g0174others(5): Show | 8 | HG01884.hp1 HG02015.hp1 HG02145.hp1 others(5): Show |
intron_variant | MODIFIER | c.2347+423_2347+424i others(10): Show |
DLG3 | ENSG00000082458.12 | transcript | ENST00000374360.8 | protein_coding | 18/18 | INFO_REALIGN_3_PRIME | chrX | 70501409 | |||||
| chrX:70501409
|
C | CTGTGTGT others(3): Show |
3 | a0001c0001t0001g0147a0001c0001t0001g0159a0001c0001t0001g0215 | 3 | HG00735.hp1 HG04204.hp1 NA19064.hp1 |
intron_variant | MODIFIER | c.2347+423_2347+424i others(12): Show |
DLG3 | ENSG00000082458.12 | transcript | ENST00000374360.8 | protein_coding | 18/18 | INFO_REALIGN_3_PRIME | chrX | 70501409 | |||||
| chrX:70501409
|
C | CTGTGTGT others(5): Show |
55 | a0001c0001t0001g0015a0001c0001t0001g0016a0001c0001t0001g0017others(52): Show | 60 | HG00621.hp1 HG01109.hp1 HG01123.hp1 others(57): Show |
intron_variant | MODIFIER | c.2347+423_2347+424i others(14): Show |
DLG3 | ENSG00000082458.12 | transcript | ENST00000374360.8 | protein_coding | 18/18 | INFO_REALIGN_3_PRIME | chrX | 70501409 | |||||
| chrX:70501409
|
C | CTGTGTGT others(7): Show |
30 | a0001c0001t0001g0022a0001c0001t0001g0133a0001c0001t0001g0140others(27): Show | 32 | HG00733.hp1 HG01070.hp2 HG01106.hp1 others(29): Show |
intron_variant | MODIFIER | c.2347+423_2347+424i others(16): Show |
DLG3 | ENSG00000082458.12 | transcript | ENST00000374360.8 | protein_coding | 18/18 | INFO_REALIGN_3_PRIME | chrX | 70501409 | |||||
| chrX:70501409
|
C | CTGTGTGT others(9): Show |
3 | a0001c0001t0001g0152a0001c0001t0001g0198a0001c0001t0025g0139 | 3 | HG02717.hp1 NA18941.hp2 NA18946.hp1 |
intron_variant | MODIFIER | c.2347+423_2347+424i others(18): Show |
DLG3 | ENSG00000082458.12 | transcript | ENST00000374360.8 | protein_coding | 18/18 | INFO_REALIGN_3_PRIME | chrX | 70501409 | |||||
| chrX:70501409
|
C | CTGTGTGT others(13): Show |
1 | a0001c0001t0001g0148 | 1 | NA18980.hp1 | intron_variant | MODIFIER | c.2347+423_2347+424i others(22): Show |
DLG3 | ENSG00000082458.12 | transcript | ENST00000374360.8 | protein_coding | 18/18 | INFO_REALIGN_3_PRIME | chrX | 70501409 | |||||
| chrX:70501411
|
GTC | G | 1 | a0001c0001t0001g0059 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.2347+424_2347+425d others(4): Show |
DLG3 | ENSG00000082458.12 | transcript | ENST00000374360.8 | protein_coding | 18/18 | INFO_REALIGN_3_PRIME | chrX | 70501411 | |||||
| chrX:70501413
|
C | CTG | 4 | a0001c0001t0002g0104a0001c0001t0002g0106a0001c0001t0024g0052others(1): Show | 4 | HG01081.hp2 HG01934.hp1 NA18906.hp2 others(1): Show |
intron_variant | MODIFIER | c.2347+452_2347+453d others(4): Show |
DLG3 | ENSG00000082458.12 | transcript | ENST00000374360.8 | protein_coding | 18/18 | INFO_REALIGN_3_PRIME | chrX | 70501413 | |||||
| chrX:70501413
|
C | CTGTCTGT others(7): Show |
1 | a0001c0001t0005g0037 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.2347+427_2347+428i others(16): Show |
DLG3 | ENSG00000082458.12 | transcript | ENST00000374360.8 | protein_coding | 18/18 | INFO_REALIGN_3_PRIME | chrX | 70501413 | |||||
| chrX:70501413
|
C | CTGTCTGT others(9): Show |
1 | a0001c0001t0003g0036 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.2347+427_2347+428i others(18): Show |
DLG3 | ENSG00000082458.12 | transcript | ENST00000374360.8 | protein_coding | 18/18 | INFO_REALIGN_3_PRIME | chrX | 70501413 | |||||
| chrX:70501413
|
C | CTGTCTGT others(11): Show |
8 | a0001c0001t0001g0038a0001c0001t0003g0008a0001c0001t0003g0028others(5): Show | 9 | HG00099.hp1 HG00642.hp1 HG00741.hp1 others(6): Show |
intron_variant | MODIFIER | c.2347+427_2347+428i others(20): Show |
DLG3 | ENSG00000082458.12 | transcript | ENST00000374360.8 | protein_coding | 18/18 | INFO_REALIGN_3_PRIME | chrX | 70501413 | |||||
| chrX:70501413
|
C | CTGTCTGT others(15): Show |
2 | a0001c0001t0003g0031a0001c0001t0003g0032 | 2 | HG01123.hp2 HG03704.hp1 |
intron_variant | MODIFIER | c.2347+427_2347+428i others(24): Show |
DLG3 | ENSG00000082458.12 | transcript | ENST00000374360.8 | protein_coding | 18/18 | INFO_REALIGN_3_PRIME | chrX | 70501413 | |||||
| chrX:70501413
|
C | CTGTG | 6 | a0001c0002t0005g0039a0001c0002t0005g0040a0001c0002t0005g0041others(3): Show | 6 | HG01167.hp1 HG01169.hp1 HG02486.hp1 others(3): Show |
intron_variant | MODIFIER | c.2347+450_2347+453d others(6): Show |
DLG3 | ENSG00000082458.12 | transcript | ENST00000374360.8 | protein_coding | 18/18 | INFO_REALIGN_3_PRIME | chrX | 70501413 | |||||
| chrX:70501413
|
C | CTGTGTGT others(5): Show |
8 | a0001c0001t0001g0026a0001c0001t0001g0137a0001c0001t0001g0173others(5): Show | 8 | HG00738.hp1 HG01255.hp1 HG03453.hp2 others(5): Show |
intron_variant | MODIFIER | c.2347+442_2347+453d others(14): Show |
DLG3 | ENSG00000082458.12 | transcript | ENST00000374360.8 | protein_coding | 18/18 | INFO_REALIGN_3_PRIME | chrX | 70501413 | |||||
| chrX:70501413
|
C | CTGTGTGT others(7): Show |
4 | a0001c0001t0001g0048a0001c0001t0001g0049a0001c0001t0001g0204others(1): Show | 4 | HG02622.hp2 HG02630.hp2 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.2347+440_2347+453d others(16): Show |
DLG3 | ENSG00000082458.12 | transcript | ENST00000374360.8 | protein_coding | 18/18 | INFO_REALIGN_3_PRIME | chrX | 70501413 | |||||
| chrX:70501413
|
C | CTGTGTGT others(9): Show |
12 | a0001c0001t0001g0044a0001c0001t0001g0045a0001c0001t0001g0046others(9): Show | 12 | HG02451.hp1 HG02559.hp1 HG02572.hp1 others(9): Show |
intron_variant | MODIFIER | c.2347+438_2347+453d others(18): Show |
DLG3 | ENSG00000082458.12 | transcript | ENST00000374360.8 | protein_coding | 18/18 | INFO_REALIGN_3_PRIME | chrX | 70501413 | |||||
| chrX:70501413
|
C | CTGTGTGT others(11): Show |
1 | a0001c0001t0007g0178 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.2347+436_2347+453d others(20): Show |
DLG3 | ENSG00000082458.12 | transcript | ENST00000374360.8 | protein_coding | 18/18 | INFO_REALIGN_3_PRIME | chrX | 70501413 | |||||
| chrX:70501413
|
C | CTGTGTGT others(15): Show |
1 | a0001c0001t0001g0029 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.2347+432_2347+453d others(24): Show |
DLG3 | ENSG00000082458.12 | transcript | ENST00000374360.8 | protein_coding | 18/18 | INFO_REALIGN_3_PRIME | chrX | 70501413 | |||||
| chrX:70501413
|
C | G | 102 | a0001c0001t0001g0015a0001c0001t0001g0016a0001c0001t0001g0017others(99): Show | 109 | HG00621.hp1 HG00733.hp1 HG00735.hp1 others(106): Show |
intron_variant | MODIFIER | c.2347+424C>G | DLG3 | ENSG00000082458.12 | transcript | ENST00000374360.8 | protein_coding | 18/18 | chrX | 70501413 | ||||||
| chrX:70501417
|
G | C | 1 | a0001c0001t0002g0094 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.2347+428G>C | DLG3 | ENSG00000082458.12 | transcript | ENST00000374360.8 | protein_coding | 18/18 | chrX | 70501417 | ||||||
| chrX:70501627
|
C | G | 6 | a0001c0002t0005g0039a0001c0002t0005g0040a0001c0002t0005g0041others(3): Show | 6 | HG01167.hp1 HG01169.hp1 HG02486.hp1 others(3): Show |
intron_variant | MODIFIER | c.2348-536C>G | DLG3 | ENSG00000082458.12 | transcript | ENST00000374360.8 | protein_coding | 18/18 | chrX | 70501627 | ||||||
| chrX:70501629
|
C | T | 1 | a0001c0001t0002g0128 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.2348-534C>T | DLG3 | ENSG00000082458.12 | transcript | ENST00000374360.8 | protein_coding | 18/18 | chrX | 70501629 | ||||||
| chrX:70501795
|
C | G | 2 | a0001c0001t0001g0207a0001c0001t0001g0211 | 2 | HG01070.hp2 HG01346.hp1 |
intron_variant | MODIFIER | c.2348-368C>G | DLG3 | ENSG00000082458.12 | transcript | ENST00000374360.8 | protein_coding | 18/18 | chrX | 70501795 | ||||||
| chrX:70501863
|
A | G | 1 | a0001c0001t0001g0163 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.2348-300A>G | DLG3 | ENSG00000082458.12 | transcript | ENST00000374360.8 | protein_coding | 18/18 | chrX | 70501863 | ||||||
| chrX:70501940
|
C | A | 1 | a0003c0009t0002g0065 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.2348-223C>A | DLG3 | ENSG00000082458.12 | transcript | ENST00000374360.8 | protein_coding | 18/18 | chrX | 70501940 | ||||||
| chrX:70502069
|
G | C | 1 | a0001c0001t0002g0106 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.2348-94G>C | DLG3 | ENSG00000082458.12 | transcript | ENST00000374360.8 | protein_coding | 18/18 | chrX | 70502069 | ||||||
| chrX:70502093
|
G | A | 6 | a0001c0001t0004g0119a0001c0001t0004g0221a0001c0001t0004g0222others(3): Show | 6 | HG02055.hp1 HG02257.hp2 HG02922.hp1 others(3): Show |
intron_variant | MODIFIER | c.2348-70G>A | DLG3 | ENSG00000082458.12 | transcript | ENST00000374360.8 | protein_coding | 18/18 | chrX | 70502093 |