Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| 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 | 276 | 70 | 43 | 120 | 11 | 30 | 97 | DLG3_chrX_70439835_70510490 | DLG3 | MHKHQ others(812): Show |
chrX | 70439835 | 70510490 |
| a0002 | 0/0 | 817 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | DLG3_chrX_70439835_70510490 | DLG3 | MHKHQ others(812): Show |
chrX | 70439835 | 70510490 |
| a0003 | 0/0 | 338 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | DLG3_chrX_70439835_70510490 | DLG3 | MHKHQ others(333): Show |
chrX | 70439835 | 70510490 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 2451 | 269 | 66 | 41 | 119 | 11 | 30 | DLG3_chrX_70439835_70510490 | DLG3 | ATGCA others(2446): Show |
chrX | 70439835 | 70510490 | ||
| a0001c0002 | 0/0 | 2451 | 6 | 4 | 2 | 0 | 0 | 0 | DLG3_chrX_70439835_70510490 | DLG3 | ATGCA others(2446): Show |
chrX | 70439835 | 70510490 | ||
| a0001c0004 | 0/0 | 2451 | 1 | 0 | 0 | 1 | 0 | 0 | DLG3_chrX_70439835_70510490 | DLG3 | ATGCA others(2446): Show |
chrX | 70439835 | 70510490 | ||
| a0002c0005 | 0/0 | 2451 | 1 | 0 | 1 | 0 | 0 | 0 | DLG3_chrX_70439835_70510490 | DLG3 | ATGCA others(2446): Show |
chrX | 70439835 | 70510490 | ||
| a0003c0003 | 0/0 | 2451 | 1 | 0 | 0 | 1 | 0 | 0 | DLG3_chrX_70439835_70510490 | DLG3 | ATGCA others(2446): Show |
chrX | 70439835 | 70510490 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/0 | 6042 | 116 | 42 | 15 | 47 | 3 | 9 | DLG3_chrX_70439835_70510490 | DLG3 | ACTCC others(6037): Show |
chrX | 70439835 | 70510490 |
| a0001c0001t0002 | 1/0 | 6042 | 100 | 5 | 14 | 62 | 6 | 12 | DLG3_chrX_70439835_70510490 | DLG3 | ACTCC others(6037): Show |
chrX | 70439835 | 70510490 |
| a0001c0001t0003 | 0/0 | 6042 | 12 | 1 | 6 | 0 | 1 | 4 | DLG3_chrX_70439835_70510490 | DLG3 | ACTCC others(6037): Show |
chrX | 70439835 | 70510490 |
| a0001c0001t0004 | 0/0 | 6042 | 7 | 7 | 0 | 0 | 0 | 0 | DLG3_chrX_70439835_70510490 | DLG3 | ACTCC others(6037): Show |
chrX | 70439835 | 70510490 |
| a0001c0001t0005 | 0/0 | 6043 | 5 | 0 | 0 | 3 | 0 | 2 | DLG3_chrX_70439835_70510490 | DLG3 | ACTCC others(6038): Show |
chrX | 70439835 | 70510490 |
| a0001c0001t0006 | 0/0 | 6048 | 4 | 4 | 0 | 0 | 0 | 0 | DLG3_chrX_70439835_70510490 | DLG3 | ACTCC others(6043): Show |
chrX | 70439835 | 70510490 |
| a0001c0001t0007 | 0/0 | 6041 | 4 | 0 | 0 | 4 | 0 | 0 | DLG3_chrX_70439835_70510490 | DLG3 | ACTCC others(6036): Show |
chrX | 70439835 | 70510490 |
| a0001c0001t0008 | 0/0 | 6030 | 4 | 0 | 4 | 0 | 0 | 0 | DLG3_chrX_70439835_70510490 | DLG3 | ACTCC others(6025): Show |
chrX | 70439835 | 70510490 |
| a0001c0001t0009 | 0/0 | 6042 | 3 | 3 | 0 | 0 | 0 | 0 | DLG3_chrX_70439835_70510490 | DLG3 | ACTCC others(6037): Show |
chrX | 70439835 | 70510490 |
| a0001c0001t0010 | 0/1 | 6042 | 3 | 0 | 1 | 0 | 1 | 0 | DLG3_chrX_70439835_70510490 | DLG3 | ACTCC others(6037): Show |
chrX | 70439835 | 70510490 |
| a0001c0001t0011 | 0/0 | 6042 | 1 | 0 | 0 | 0 | 0 | 1 | DLG3_chrX_70439835_70510490 | DLG3 | ACTCC others(6037): Show |
chrX | 70439835 | 70510490 |
| a0001c0001t0012 | 0/0 | 6042 | 1 | 0 | 0 | 1 | 0 | 0 | DLG3_chrX_70439835_70510490 | DLG3 | ACTCC others(6037): Show |
chrX | 70439835 | 70510490 |
| a0001c0001t0013 | 0/0 | 6042 | 1 | 0 | 0 | 1 | 0 | 0 | DLG3_chrX_70439835_70510490 | DLG3 | ACTCC others(6037): Show |
chrX | 70439835 | 70510490 |
| a0001c0001t0014 | 0/0 | 6042 | 1 | 1 | 0 | 0 | 0 | 0 | DLG3_chrX_70439835_70510490 | DLG3 | ACTCC others(6037): Show |
chrX | 70439835 | 70510490 |
| a0001c0001t0015 | 0/0 | 6042 | 1 | 0 | 0 | 0 | 0 | 1 | DLG3_chrX_70439835_70510490 | DLG3 | ACTCC others(6037): Show |
chrX | 70439835 | 70510490 |
| a0001c0001t0016 | 0/0 | 6042 | 1 | 0 | 1 | 0 | 0 | 0 | DLG3_chrX_70439835_70510490 | DLG3 | ACTCC others(6037): Show |
chrX | 70439835 | 70510490 |
| a0001c0001t0017 | 0/0 | 6042 | 1 | 0 | 0 | 0 | 0 | 1 | DLG3_chrX_70439835_70510490 | DLG3 | ACTCC others(6037): Show |
chrX | 70439835 | 70510490 |
| a0001c0001t0018 | 0/0 | 6042 | 1 | 1 | 0 | 0 | 0 | 0 | DLG3_chrX_70439835_70510490 | DLG3 | ACTCC others(6037): Show |
chrX | 70439835 | 70510490 |
| a0001c0001t0019 | 0/0 | 6043 | 1 | 1 | 0 | 0 | 0 | 0 | DLG3_chrX_70439835_70510490 | DLG3 | ACTCC others(6038): Show |
chrX | 70439835 | 70510490 |
| a0001c0001t0020 | 0/0 | 6043 | 1 | 1 | 0 | 0 | 0 | 0 | DLG3_chrX_70439835_70510490 | DLG3 | ACTCC others(6038): Show |
chrX | 70439835 | 70510490 |
| a0001c0001t0021 | 0/0 | 6042 | 1 | 0 | 0 | 1 | 0 | 0 | DLG3_chrX_70439835_70510490 | DLG3 | ACTCC others(6037): Show |
chrX | 70439835 | 70510490 |
| a0001c0002t0001 | 0/0 | 6042 | 6 | 4 | 2 | 0 | 0 | 0 | DLG3_chrX_70439835_70510490 | DLG3 | ACTCC others(6037): Show |
chrX | 70439835 | 70510490 |
| a0001c0004t0002 | 0/0 | 6042 | 1 | 0 | 0 | 1 | 0 | 0 | DLG3_chrX_70439835_70510490 | DLG3 | ACTCC others(6037): Show |
chrX | 70439835 | 70510490 |
| a0002c0005t0002 | 0/0 | 6042 | 1 | 0 | 1 | 0 | 0 | 0 | DLG3_chrX_70439835_70510490 | DLG3 | ACTCC others(6037): Show |
chrX | 70439835 | 70510490 |
| a0003c0003t0001 | 0/0 | 6042 | 1 | 0 | 0 | 1 | 0 | 0 | DLG3_chrX_70439835_70510490 | DLG3 | ACTCC others(6037): Show |
chrX | 70439835 | 70510490 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0007 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| a0001c0001t0001g0022 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| a0001c0001t0001g0023 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| a0001c0001t0001g0024 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| a0001c0001t0001g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| a0001c0001t0001g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| a0001c0001t0001g0028 | 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 |
| a0001c0001t0001g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| a0001c0001t0001g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| a0001c0001t0001g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| a0001c0001t0001g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| a0001c0001t0001g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| a0001c0001t0001g0037 | 0/0 | 1 | 1 | 0 | 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 | 0 | 1 | 0 | 0 | 0 | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| a0001c0001t0001g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| a0001c0001t0001g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| a0001c0001t0001g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| a0001c0001t0001g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| a0001c0001t0001g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| a0001c0001t0001g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| a0001c0001t0001g0060 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| a0001c0001t0001g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| a0001c0001t0001g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| a0001c0001t0001g0129 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| a0001c0001t0001g0131 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| a0001c0001t0001g0132 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| a0001c0001t0001g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| a0001c0001t0001g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| a0001c0001t0001g0136 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| a0001c0001t0001g0138 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| a0001c0001t0001g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| a0001c0001t0001g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| a0001c0001t0001g0142 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| a0001c0001t0001g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| a0001c0001t0001g0144 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| a0001c0001t0001g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| a0001c0001t0001g0146 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| a0001c0001t0001g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | 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 |
| a0001c0001t0001g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| a0001c0001t0001g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| a0001c0001t0001g0155 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| a0001c0001t0001g0156 | 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 | 1 | 0 | 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 | 0 | 0 | 0 | 1 | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| a0001c0001t0001g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| a0001c0001t0001g0167 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| a0001c0001t0001g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| a0001c0001t0001g0171 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| a0001c0001t0001g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| a0001c0001t0001g0175 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| a0001c0001t0001g0177 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| a0001c0001t0001g0178 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| a0001c0001t0001g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| a0001c0001t0001g0183 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| a0001c0001t0001g0184 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| a0001c0001t0001g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| a0001c0001t0001g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| a0001c0001t0001g0187 | 0/0 | 1 | 0 | 0 | 1 | 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 | 0 | 0 | 1 | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| a0001c0001t0001g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| a0001c0001t0001g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| a0001c0001t0001g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | 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 | 0 | 1 | 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 | 1 | 0 | 0 | 0 | 0 | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| a0001c0001t0001g0208 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| a0001c0001t0001g0209 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| a0001c0001t0001g0210 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| a0001c0001t0001g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| a0001c0001t0001g0214 | 0/0 | 1 | 0 | 1 | 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 | 1 | 0 | 0 | 0 | 0 | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| a0001c0001t0001g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| a0001c0001t0001g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| a0001c0001t0001g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | 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 |
| a0001c0001t0001g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| a0001c0001t0001g0227 | 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 |
| a0001c0001t0001g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| a0001c0001t0001g0234 | 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 |
| a0001c0001t0001g0238 | 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 |
| a0001c0001t0001g0241 | 0/0 | 1 | 1 | 0 | 0 | 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 |
| a0001c0001t0002g0005 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| a0001c0001t0002g0006 | 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 | 2 | 0 | 0 | 0 | 0 | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| a0001c0001t0002g0011 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| a0001c0001t0002g0012 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| a0001c0001t0002g0013 | 0/0 | 2 | 0 | 0 | 1 | 1 | 0 | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| a0001c0001t0002g0014 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| a0001c0001t0002g0015 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| a0001c0001t0002g0016 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| a0001c0001t0002g0017 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| a0001c0001t0002g0019 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| a0001c0001t0002g0020 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| a0001c0001t0002g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| a0001c0001t0002g0061 | 0/0 | 1 | 0 | 0 | 1 | 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 |
| a0001c0001t0002g0066 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| a0001c0001t0002g0068 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| a0001c0001t0002g0070 | 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 |
| a0001c0001t0002g0073 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| a0001c0001t0002g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | 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 | 0 | 0 | 1 | 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 |
| a0001c0001t0002g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| a0001c0001t0002g0085 | 0/0 | 1 | 0 | 0 | 1 | 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 | 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 | 1 | 0 | 0 | 0 | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| a0001c0001t0002g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| a0001c0001t0002g0095 | 0/0 | 1 | 0 | 1 | 0 | 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 | 1 | 0 | 0 | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| a0001c0001t0002g0101 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| a0001c0001t0002g0102 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| a0001c0001t0002g0103 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| a0001c0001t0002g0104 | 0/0 | 1 | 0 | 0 | 0 | 1 | 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 | 0 | 1 | 0 | 0 | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| a0001c0001t0002g0109 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| a0001c0001t0002g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| a0001c0001t0002g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| a0001c0001t0002g0112 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | 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 | 1 | 0 | 0 | 0 | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| a0001c0001t0002g0115 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| a0001c0001t0002g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| a0001c0001t0002g0119 | 0/0 | 1 | 0 | 1 | 0 | 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 |
| a0001c0001t0002g0124 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| a0001c0001t0002g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| a0001c0001t0002g0127 | 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 |
| a0001c0001t0002g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| a0001c0001t0002g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| a0001c0001t0002g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| a0001c0001t0003g0004 | 0/0 | 3 | 0 | 1 | 0 | 1 | 1 | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| a0001c0001t0003g0036 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| a0001c0001t0003g0038 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| a0001c0001t0003g0039 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| a0001c0001t0003g0040 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| a0001c0001t0003g0041 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| a0001c0001t0003g0042 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| a0001c0001t0003g0043 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| a0001c0001t0003g0153 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| a0001c0001t0003g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| a0001c0001t0004g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| a0001c0001t0004g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| a0001c0001t0004g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| a0001c0001t0004g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| a0001c0001t0004g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| a0001c0001t0004g0231 | 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 |
| a0001c0001t0005g0011 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| a0001c0001t0005g0018 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| a0001c0001t0005g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| a0001c0001t0005g0108 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| a0001c0001t0005g0141 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| a0001c0001t0006g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| a0001c0001t0006g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| a0001c0001t0006g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| a0001c0001t0006g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| a0001c0001t0007g0001 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| a0001c0001t0007g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| a0001c0001t0007g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| a0001c0001t0007g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| a0001c0001t0008g0008 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| a0001c0001t0008g0174 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| a0001c0001t0009g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| a0001c0001t0009g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| a0001c0001t0009g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| a0001c0001t0010g0021 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| a0001c0001t0010g0130 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| a0001c0001t0011g0116 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| a0001c0001t0012g0018 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| a0001c0001t0013g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| a0001c0001t0014g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| a0001c0001t0015g0200 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| a0001c0001t0016g0059 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| a0001c0001t0017g0133 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| a0001c0001t0018g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| a0001c0001t0019g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| a0001c0001t0020g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| a0001c0001t0021g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| a0001c0002t0001g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| a0001c0002t0001g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| a0001c0002t0001g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| a0001c0002t0001g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| a0001c0002t0001g0180 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| a0001c0002t0001g0181 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| a0001c0004t0002g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| a0002c0005t0002g0069 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| a0003c0003t0001g0170 | 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 | g0004 | EUR | GBR | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| HG00099 | hp2 | a0001 | c0001 | t0002 | g0109 | EUR | GBR | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| HG00140 | hp1 | a0001 | c0001 | t0002 | g0020 | EUR | GBR | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| HG00280 | hp1 | a0001 | c0001 | t0002 | g0104 | EUR | FIN | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| HG00438 | hp1 | a0001 | c0004 | t0002 | g0126 | EAS | CHS | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| HG00438 | hp2 | a0001 | c0001 | t0002 | g0076 | EAS | CHS | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| HG00609 | hp1 | a0001 | c0001 | t0002 | g0085 | 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 | g0038 | AMR | PUR | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| HG00673 | hp1 | a0001 | c0001 | t0002 | g0087 | EAS | CHS | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| HG00733 | hp1 | a0001 | c0001 | t0010 | g0021 | AMR | PUR | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| HG00733 | hp2 | a0001 | c0001 | t0003 | g0043 | AMR | PUR | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| HG00735 | hp1 | a0001 | c0001 | t0001 | g0214 | AMR | PUR | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| HG00735 | hp2 | a0001 | c0001 | t0002 | g0070 | AMR | PUR | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| HG00738 | hp1 | a0001 | c0001 | t0001 | g0183 | AMR | PUR | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| HG00741 | hp1 | a0001 | c0001 | t0001 | g0045 | AMR | PUR | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| HG00741 | hp2 | a0001 | c0001 | t0002 | g0095 | AMR | PUR | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| HG01069 | hp1 | a0001 | c0001 | t0003 | g0042 | AMR | PUR | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| HG01070 | hp1 | a0001 | c0001 | t0003 | g0004 | AMR | PUR | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| HG01070 | hp2 | a0001 | c0001 | t0001 | g0210 | AMR | PUR | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| HG01074 | hp1 | a0002 | c0005 | t0002 | g0069 | AMR | PUR | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| HG01081 | hp1 | a0001 | c0001 | t0002 | g0020 | AMR | PUR | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| HG01081 | hp2 | a0001 | c0001 | t0016 | g0059 | AMR | PUR | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| HG01099 | hp1 | a0001 | c0001 | t0002 | g0102 | AMR | PUR | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| HG01106 | hp1 | a0001 | c0001 | t0001 | g0129 | AMR | PUR | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| HG01109 | hp1 | a0001 | c0001 | t0001 | g0175 | AMR | PUR | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| HG01167 | hp1 | a0001 | c0002 | t0001 | g0181 | AMR | PUR | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| HG01169 | hp1 | a0001 | c0002 | t0001 | g0180 | AMR | PUR | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| HG01169 | hp2 | a0001 | c0001 | t0002 | g0103 | AMR | PUR | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| HG01175 | hp1 | a0001 | c0001 | t0001 | g0138 | AMR | PUR | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| HG01175 | hp2 | a0001 | c0001 | t0002 | g0093 | AMR | PUR | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| HG01192 | hp1 | a0001 | c0001 | t0001 | g0136 | AMR | PUR | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| HG01243 | hp1 | a0001 | c0001 | t0001 | g0208 | AMR | PUR | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| HG01255 | hp1 | a0001 | c0001 | t0001 | g0171 | 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 | t0008 | g0174 | AMR | CLM | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| HG01257 | hp2 | a0001 | c0001 | t0002 | g0096 | AMR | CLM | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| HG01258 | hp1 | a0001 | c0001 | t0008 | g0008 | AMR | CLM | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| HG01261 | hp1 | a0001 | c0001 | t0001 | g0142 | AMR | CLM | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| HG01346 | hp1 | a0001 | c0001 | t0001 | g0205 | AMR | CLM | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| HG01346 | hp2 | a0001 | c0001 | t0002 | g0119 | AMR | CLM | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| HG01358 | hp1 | a0001 | c0001 | t0001 | g0215 | AMR | CLM | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| HG01361 | hp1 | a0001 | c0001 | t0001 | g0144 | AMR | CLM | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| HG01361 | hp2 | a0001 | c0001 | t0002 | g0106 | 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 | g0017 | EUR | IBS | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| HG01516 | hp1 | a0001 | c0001 | t0002 | g0013 | EUR | IBS | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| HG01516 | hp2 | a0001 | c0001 | t0001 | g0178 | EUR | IBS | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| HG01517 | hp1 | a0001 | c0001 | t0001 | g0177 | EUR | IBS | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| HG01517 | hp2 | a0001 | c0001 | t0002 | g0017 | EUR | IBS | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| HG01884 | hp1 | a0001 | c0001 | t0001 | g0224 | 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 | t0001 | g0044 | AFR | ACB | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| HG01891 | hp2 | a0001 | c0001 | t0001 | g0239 | AFR | ACB | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| HG01928 | hp1 | a0001 | c0001 | t0001 | g0160 | AMR | PEL | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| HG01934 | hp1 | a0001 | c0001 | t0002 | g0105 | 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 | t0008 | g0008 | AMR | PEL | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| HG01993 | hp1 | a0001 | c0001 | t0002 | g0114 | AMR | PEL | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| HG01993 | hp2 | a0001 | c0001 | t0003 | g0040 | AMR | PEL | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| HG02015 | hp1 | a0001 | c0001 | t0001 | g0026 | EAS | KHV | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| HG02027 | hp1 | a0001 | c0001 | t0002 | g0218 | 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 | g0219 | AFR | ACB | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| HG02056 | hp1 | a0001 | c0001 | t0002 | g0169 | EAS | KHV | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| HG02071 | hp1 | a0001 | c0001 | t0002 | g0110 | EAS | KHV | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| HG02074 | hp1 | a0001 | c0001 | t0002 | g0034 | EAS | KHV | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| HG02083 | hp1 | a0001 | c0001 | t0002 | g0006 | EAS | KHV | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| HG02129 | hp1 | a0001 | c0001 | t0002 | g0090 | EAS | KHV | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| HG02132 | hp1 | a0001 | c0001 | t0002 | g0127 | EAS | KHV | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| HG02135 | hp1 | a0001 | c0001 | t0002 | g0019 | EAS | KHV | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| HG02145 | hp1 | a0001 | c0001 | t0020 | g0222 | AFR | ACB | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| HG02155 | hp1 | a0001 | c0001 | t0001 | g0161 | EAS | CDX | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| HG02155 | hp2 | a0001 | c0001 | t0001 | g0064 | 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 | g0086 | EAS | CDX | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| HG02257 | hp1 | a0001 | c0001 | t0001 | g0024 | AFR | ACB | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| HG02257 | hp2 | a0001 | c0001 | t0004 | g0231 | AFR | ACB | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| HG02258 | hp1 | a0001 | c0001 | t0001 | g0028 | AFR | ACB | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| HG02280 | hp1 | a0001 | c0001 | t0001 | g0037 | AFR | ACB | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| HG02280 | hp2 | a0001 | c0001 | t0006 | g0176 | AFR | ACB | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| HG02451 | hp1 | a0001 | c0001 | t0001 | g0229 | AFR | ACB | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| HG02451 | hp2 | a0001 | c0001 | t0001 | g0237 | 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 | g0113 | EAS | KHV | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| HG02572 | hp1 | a0001 | c0001 | t0001 | g0054 | AFR | GWD | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| HG02602 | hp1 | a0001 | c0001 | t0002 | g0124 | SAS | PJL | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| HG02615 | hp1 | a0001 | c0001 | t0001 | g0202 | AFR | GWD | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| HG02615 | hp2 | a0001 | c0001 | t0001 | g0053 | AFR | GWD | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| HG02622 | hp1 | a0001 | c0001 | t0001 | g0241 | AFR | GWD | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| HG02622 | hp2 | a0001 | c0001 | t0001 | g0056 | AFR | GWD | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| HG02630 | hp1 | a0001 | c0001 | t0001 | g0185 | AFR | GWD | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| HG02630 | hp2 | a0001 | c0001 | t0001 | g0201 | AFR | GWD | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| HG02647 | hp1 | a0001 | c0001 | t0001 | g0140 | AFR | GWD | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| HG02683 | hp1 | a0001 | c0001 | t0002 | g0068 | SAS | PJL | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| HG02683 | hp2 | a0001 | c0001 | t0002 | g0080 | 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 | t0018 | g0137 | AFR | GWD | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| HG02735 | hp1 | a0001 | c0001 | t0001 | g0060 | SAS | PJL | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| HG02738 | hp1 | a0001 | c0001 | t0001 | g0155 | SAS | PJL | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| HG02809 | hp1 | a0001 | c0001 | t0001 | g0207 | AFR | GWD | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| HG02809 | hp2 | a0001 | c0001 | t0002 | g0010 | AFR | GWD | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| HG02886 | hp1 | a0001 | c0001 | t0001 | g0216 | AFR | GWD | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| HG02886 | hp2 | a0001 | c0001 | t0014 | g0225 | AFR | GWD | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| HG02895 | hp1 | a0001 | c0002 | t0001 | g0048 | AFR | GWD | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| HG02896 | hp1 | a0001 | c0001 | t0002 | g0010 | AFR | GWD | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| HG02896 | hp2 | a0001 | c0001 | t0001 | g0227 | AFR | GWD | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| HG02897 | hp1 | a0001 | c0001 | t0001 | g0226 | AFR | GWD | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| HG02897 | hp2 | a0001 | c0002 | t0001 | g0047 | AFR | GWD | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| HG02922 | hp1 | a0001 | c0001 | t0004 | g0230 | AFR | ESN | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| HG02922 | hp2 | a0001 | c0001 | t0001 | g0027 | AFR | ESN | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| HG02965 | hp1 | a0001 | c0001 | t0001 | g0024 | AFR | ESN | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| HG02970 | hp1 | a0001 | c0001 | t0001 | g0238 | AFR | ESN | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| HG02970 | hp2 | a0001 | c0001 | t0001 | g0235 | AFR | ESN | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| HG02976 | hp1 | a0001 | c0001 | t0001 | g0172 | 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 | g0041 | SAS | PJL | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| HG03041 | hp1 | a0001 | c0001 | t0001 | g0223 | AFR | GWD | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| HG03041 | hp2 | a0001 | c0001 | t0001 | g0051 | AFR | GWD | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| HG03098 | hp1 | a0001 | c0001 | t0004 | g0179 | AFR | MSL | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| HG03130 | hp1 | a0001 | c0001 | t0001 | g0055 | AFR | ESN | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| HG03139 | hp1 | a0001 | c0001 | t0001 | g0212 | AFR | ESN | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| HG03209 | hp1 | a0001 | c0001 | t0001 | g0228 | AFR | MSL | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| HG03225 | hp1 | a0001 | c0001 | t0001 | g0221 | AFR | MSL | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| HG03239 | hp1 | a0001 | c0001 | t0002 | g0112 | SAS | PJL | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| HG03239 | hp2 | a0001 | c0001 | t0003 | g0153 | SAS | PJL | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| HG03453 | hp1 | a0001 | c0001 | t0001 | g0203 | AFR | MSL | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| HG03453 | hp2 | a0001 | c0001 | t0001 | g0233 | AFR | MSL | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| HG03486 | hp1 | a0001 | c0002 | t0001 | g0049 | AFR | MSL | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| HG03486 | hp2 | a0001 | c0001 | t0006 | g0173 | AFR | MSL | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| HG03490 | hp1 | a0001 | c0001 | t0001 | g0199 | SAS | PJL | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| HG03491 | hp1 | a0001 | c0001 | t0001 | g0131 | SAS | PJL | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| HG03491 | hp2 | a0001 | c0001 | t0002 | g0081 | SAS | PJL | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| HG03492 | hp1 | a0001 | c0001 | t0001 | g0132 | SAS | PJL | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| HG03540 | hp1 | a0001 | c0001 | t0004 | g0220 | AFR | GWD | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| HG03540 | hp2 | a0001 | c0001 | t0009 | g0213 | AFR | GWD | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| HG03579 | hp1 | a0001 | c0001 | t0001 | g0206 | AFR | MSL | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| HG03654 | hp1 | a0001 | c0001 | t0002 | g0115 | SAS | PJL | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| HG03669 | hp1 | a0001 | c0001 | t0003 | g0036 | SAS | PJL | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| HG03669 | hp2 | a0001 | c0001 | t0005 | g0108 | SAS | PJL | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| HG03688 | hp1 | a0001 | c0001 | t0011 | g0116 | SAS | STU | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| HG03704 | hp1 | a0001 | c0001 | t0003 | g0004 | SAS | PJL | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| HG03704 | hp2 | a0001 | c0001 | t0002 | g0101 | SAS | PJL | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| HG03710 | hp1 | a0001 | c0001 | t0001 | g0164 | SAS | PJL | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| HG03831 | hp1 | a0001 | c0001 | t0002 | g0062 | SAS | BEB | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| HG03831 | hp2 | a0001 | c0001 | t0001 | g0184 | SAS | BEB | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| HG03927 | hp1 | a0001 | c0001 | t0017 | g0133 | SAS | BEB | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| HG03927 | hp2 | a0001 | c0001 | t0001 | g0167 | SAS | BEB | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| HG03942 | hp1 | a0001 | c0001 | t0015 | g0200 | SAS | BEB | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| HG04115 | hp1 | a0001 | c0001 | t0005 | g0141 | SAS | STU | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| HG04199 | hp1 | a0001 | c0001 | t0002 | g0079 | SAS | STU | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| HG04204 | hp1 | a0001 | c0001 | t0001 | g0146 | SAS | STU | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| HG04228 | hp1 | a0001 | c0001 | t0002 | g0073 | SAS | STU | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| NA18522 | hp1 | a0001 | c0001 | t0001 | g0135 | AFR | YRI | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| NA18612 | hp1 | a0001 | c0001 | t0002 | g0074 | EAS | CHB | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| NA18747 | hp1 | a0001 | c0001 | t0001 | g0162 | EAS | CHB | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| NA18906 | hp1 | a0001 | c0001 | t0004 | g0232 | AFR | YRI | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| NA18906 | hp2 | a0001 | c0001 | t0019 | g0058 | AFR | YRI | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| NA18940 | hp1 | a0001 | c0001 | t0001 | g0190 | 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 | g0143 | EAS | JPT | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| NA18942 | hp1 | a0001 | c0001 | t0007 | g0067 | EAS | JPT | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| NA18942 | hp2 | a0001 | c0001 | t0001 | g0165 | EAS | JPT | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| NA18943 | hp1 | a0001 | c0001 | t0002 | g0005 | EAS | JPT | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| NA18944 | hp1 | a0001 | c0001 | t0001 | g0022 | EAS | JPT | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| NA18945 | hp1 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| NA18946 | hp1 | a0001 | c0001 | t0001 | g0188 | EAS | JPT | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| NA18946 | hp2 | a0001 | c0001 | t0001 | g0163 | EAS | JPT | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| NA18947 | hp1 | a0001 | c0001 | t0002 | g0111 | EAS | JPT | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| NA18947 | hp2 | a0001 | c0001 | t0001 | g0063 | EAS | JPT | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| NA18948 | hp1 | a0001 | c0001 | t0002 | g0016 | EAS | JPT | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| NA18949 | hp1 | a0001 | c0001 | t0021 | g0083 | 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 | g0005 | EAS | JPT | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| NA18950 | hp2 | a0001 | c0001 | t0001 | g0031 | EAS | JPT | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| NA18951 | hp1 | a0001 | c0001 | t0002 | g0016 | EAS | JPT | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| NA18951 | hp2 | a0001 | c0001 | t0001 | g0154 | EAS | JPT | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| NA18952 | hp1 | a0001 | c0001 | t0002 | g0005 | EAS | JPT | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| NA18953 | hp1 | a0001 | c0001 | t0001 | g0159 | EAS | JPT | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| NA18956 | hp1 | a0001 | c0001 | t0002 | g0015 | EAS | JPT | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| NA18956 | hp2 | a0001 | c0001 | t0002 | g0151 | 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 | g0012 | EAS | JPT | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| NA18959 | hp1 | a0003 | c0003 | t0001 | g0170 | 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 | g0012 | 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 | g0094 | EAS | JPT | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| NA18964 | hp2 | a0001 | c0001 | t0001 | g0168 | EAS | JPT | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| NA18966 | hp1 | a0001 | c0001 | t0005 | g0018 | EAS | JPT | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| NA18967 | hp1 | a0001 | c0001 | t0001 | g0186 | EAS | JPT | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| NA18968 | hp1 | a0001 | c0001 | t0001 | g0197 | EAS | JPT | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| NA18968 | hp2 | a0001 | c0001 | t0002 | g0019 | EAS | JPT | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| NA18970 | hp1 | a0001 | c0001 | t0002 | g0014 | 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 | g0187 | EAS | JPT | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| NA18972 | hp2 | a0001 | c0001 | t0002 | g0088 | EAS | JPT | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| NA18974 | hp1 | a0001 | c0001 | t0001 | g0007 | 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 | g0147 | EAS | JPT | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| NA18980 | hp2 | a0001 | c0001 | t0002 | g0013 | EAS | JPT | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| NA18982 | hp1 | a0001 | c0001 | t0002 | g0125 | 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 | g0061 | EAS | JPT | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| NA18988 | hp1 | a0001 | c0001 | t0002 | g0099 | EAS | JPT | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| NA18989 | hp1 | a0001 | c0001 | t0001 | g0217 | 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 | t0005 | g0011 | EAS | JPT | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| NA18991 | hp2 | a0001 | c0001 | t0001 | g0023 | EAS | JPT | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| NA18993 | hp1 | a0001 | c0001 | t0002 | g0006 | EAS | JPT | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| NA18993 | hp2 | a0001 | c0001 | t0001 | g0157 | EAS | JPT | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| NA18994 | hp1 | a0001 | c0001 | t0007 | g0091 | 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 | g0107 | 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 | g0156 | EAS | JPT | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| NA19002 | hp1 | a0001 | c0001 | t0007 | 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 | t0007 | g0001 | EAS | JPT | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| NA19003 | hp2 | a0001 | c0001 | t0001 | g0198 | EAS | JPT | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| NA19004 | hp1 | a0001 | c0001 | t0001 | g0022 | EAS | JPT | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| NA19005 | hp1 | a0001 | c0001 | t0001 | g0030 | EAS | JPT | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| NA19007 | hp1 | a0001 | c0001 | t0002 | g0075 | EAS | JPT | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| NA19009 | hp1 | a0001 | c0001 | t0002 | g0011 | EAS | JPT | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| NA19010 | hp1 | a0001 | c0001 | t0001 | g0007 | 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 | g0150 | EAS | JPT | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| NA19011 | hp2 | a0001 | c0001 | t0005 | g0065 | EAS | JPT | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| NA19012 | hp1 | a0001 | c0001 | t0001 | g0152 | EAS | JPT | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| NA19030 | hp1 | a0001 | c0001 | t0001 | g0139 | AFR | LWK | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| NA19030 | hp2 | a0001 | c0001 | t0001 | g0033 | AFR | LWK | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| NA19043 | hp1 | a0001 | c0001 | t0004 | g0118 | AFR | LWK | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| NA19055 | hp1 | a0001 | c0001 | t0002 | g0128 | EAS | JPT | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| NA19056 | hp1 | a0001 | c0001 | t0002 | g0092 | EAS | JPT | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| NA19058 | hp1 | a0001 | c0001 | t0001 | g0182 | EAS | JPT | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| NA19060 | hp1 | a0001 | c0001 | t0001 | g0023 | EAS | JPT | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| NA19063 | hp1 | a0001 | c0001 | t0012 | g0018 | EAS | JPT | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| NA19064 | hp1 | a0001 | c0001 | t0001 | g0158 | 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 | g0189 | EAS | JPT | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| NA19065 | hp2 | a0001 | c0001 | t0002 | g0082 | EAS | JPT | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| NA19066 | hp1 | a0001 | c0001 | t0002 | g0077 | EAS | JPT | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| NA19067 | hp1 | a0001 | c0001 | t0001 | g0145 | EAS | JPT | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| NA19068 | hp1 | a0001 | c0001 | t0002 | g0078 | EAS | JPT | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| NA19070 | hp1 | a0001 | c0001 | t0002 | g0015 | EAS | JPT | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| NA19074 | hp1 | a0001 | c0001 | t0001 | g0148 | 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 | t0001 | g0035 | EAS | JPT | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| NA19077 | hp1 | a0001 | c0001 | t0002 | g0084 | 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 | g0014 | EAS | JPT | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| NA19082 | hp1 | a0001 | c0001 | t0002 | g0117 | EAS | JPT | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| NA19083 | hp1 | a0001 | c0001 | t0002 | g0089 | EAS | JPT | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| NA19085 | hp1 | a0001 | c0001 | t0013 | g0025 | EAS | JPT | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| NA19087 | hp1 | a0001 | c0001 | t0001 | g0032 | 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 | g0100 | EAS | JPT | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| NA19091 | hp1 | a0001 | c0001 | t0002 | g0006 | 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 | g0204 | AFR | YRI | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| NA20752 | hp1 | a0001 | c0001 | t0010 | g0021 | EUR | TSI | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| NA20805 | hp1 | a0001 | c0001 | t0001 | g0209 | EUR | TSI | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| NA20905 | hp1 | a0001 | c0001 | t0002 | g0066 | SAS | GIH | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| HG01123 | hp1 | a0001 | c0001 | t0008 | g0008 | AMR | CLM | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| HG01123 | hp2 | a0001 | c0001 | t0003 | g0039 | AMR | CLM | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| HG02109 | hp1 | a0001 | c0001 | t0001 | g0029 | AFR | ACB | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| HG02109 | hp2 | a0001 | c0001 | t0001 | g0236 | AFR | ACB | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| HG02486 | hp1 | a0001 | c0002 | t0001 | g0046 | AFR | ACB | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| HG02559 | hp1 | a0001 | c0001 | t0006 | g0052 | AFR | ACB | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| HG02559 | hp2 | a0001 | c0001 | t0006 | g0211 | AFR | ACB | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| HG03471 | hp1 | a0001 | c0001 | t0001 | g0234 | AFR | MSL | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| HG06807 | hp1 | a0001 | c0001 | t0001 | g0057 | AFR | USA | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| HG06807 | hp2 | a0001 | c0001 | t0009 | g0240 | AFR | USA | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| NA18955 | hp1 | a0001 | c0001 | t0001 | g0134 | EAS | JPT | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| NA20300 | hp1 | a0001 | c0001 | t0009 | g0050 | AFR | USA | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| NA20300 | hp2 | a0001 | c0001 | t0003 | g0166 | AFR | USA | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0010 | g0130 | REF | REF | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0002 | g0003 | REF | REF | DLG3_chrX_70439835_70510490 | DLG3 | chrX | 70439835 | 70510490 |
| view | 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:70450276 | C | T | 1 | a0002 | 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 | a0003 | 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 | a0003 | 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 | a0003 | 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:70451878 | T | G | 1 | a0003 | 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:70451884 | G | C | 1 | a0003 | 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 | a0003 | 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 | a0003 | 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 | a0003 | 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 | a0003 | 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 | a0003 | 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 | a0003 | 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 | a0003 | 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 | a0003 | 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:70451902 | A | T | 1 | a0003 | 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 | a0003 | 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 | a0003 | 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 |
| view | 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 | a0003c0003 | 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 | a0003c0003 | 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 | a0003c0003 | 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 | a0001c0004 | 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 |
| view | 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:70445113 | C | CCGGCGG | 1 | a0001c0001t0006 | 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 | a0001c0001t0008 | 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 | a0001c0001t0009 | 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:70445177 | G | A | 1 | a0001c0001t0011 | 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:70502424 | CT | C | 2 | a0001c0001t0007 a0001c0001t0012 |
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:70503053 | G | A | 1 | a0001c0001t0013 | 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 | a0001c0001t0021 | 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 | a0001c0001t0005 a0001c0001t0012 a0001c0001t0019 others(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:70503602 | T | A | 1 | a0001c0001t0014 | 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 | a0001c0001t0015 | 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:70504037 | T | A | 1 | a0001c0001t0010 | 2 | HG00733.hp1 NA20752.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 | 14 | a0001c0001t0001 a0001c0001t0006 a0001c0001t0008 others(11): Show |
143 | HG00621.hp1 HG00733.hp1 HG00735.hp1 others(140): 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 | 15 | a0001c0001t0001 a0001c0001t0003 a0001c0001t0006 others(12): Show |
155 | HG00099.hp1 HG00621.hp1 HG00642.hp1 others(152): 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 | a0001c0001t0016 a0001c0001t0019 |
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 | a0001c0001t0018 | 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 | a0001c0001t0017 | 1 | HG03927.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3064G>A | DLG3 | ENSG00000082458.12 | transcript | ENST00000374360.8 | protein_coding | 19/19 | 3064 | chrX | 70505333 |
| view | 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:70446003 | A | G | 24 | a0001c0001t0001g0024 a0001c0001t0001g0221 a0001c0001t0001g0223 others(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 | a0001c0001t0002g0218 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.357+490C>T | DLG3 | ENSG00000082458.12 | transcript | ENST00000374360.8 | protein_coding | 1/18 | chrX | 70446048 | |||||||
| chrX:70446244 | G | A | 1 | a0001c0001t0013g0025 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.357+686G>A | DLG3 | ENSG00000082458.12 | transcript | ENST00000374360.8 | protein_coding | 1/18 | chrX | 70446244 | |||||||
| chrX:70446273 | G | T | 1 | a0001c0001t0001g0217 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.357+715G>T | DLG3 | ENSG00000082458.12 | transcript | ENST00000374360.8 | protein_coding | 1/18 | chrX | 70446273 | |||||||
| chrX:70446437 | C | G | 1 | a0001c0001t0001g0217 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.357+879C>G | DLG3 | ENSG00000082458.12 | transcript | ENST00000374360.8 | protein_coding | 1/18 | chrX | 70446437 | |||||||
| chrX:70446480 | G | C | 1 | a0001c0001t0001g0026 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.357+922G>C | DLG3 | ENSG00000082458.12 | transcript | ENST00000374360.8 | protein_coding | 1/18 | chrX | 70446480 | |||||||
| chrX:70446747 | G | T | 1 | a0001c0001t0001g0216 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.357+1189G>T | DLG3 | ENSG00000082458.12 | transcript | ENST00000374360.8 | protein_coding | 1/18 | chrX | 70446747 | |||||||
| chrX:70446789 | T | A | 1 | a0001c0001t0001g0027 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.357+1231T>A | DLG3 | ENSG00000082458.12 | transcript | ENST00000374360.8 | protein_coding | 1/18 | chrX | 70446789 | |||||||
| chrX:70446798 | G | C | 8 | a0001c0001t0001g0028 a0001c0001t0001g0029 a0001c0001t0001g0221 others(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:70447008 | T | C | 2 | a0001c0001t0001g0030 a0001c0001t0001g0031 |
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:70447065 | C | T | 48 | a0001c0001t0001g0023 a0001c0001t0001g0024 a0001c0001t0001g0026 others(45): 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 | a0001c0001t0001g0032 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.357+1508G>C | DLG3 | ENSG00000082458.12 | transcript | ENST00000374360.8 | protein_coding | 1/18 | chrX | 70447066 | |||||||
| chrX:70447346 | T | C | 1 | a0001c0001t0001g0033 | 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 | a0001c0001t0002g0034 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.358-1528G>A | DLG3 | ENSG00000082458.12 | transcript | ENST00000374360.8 | protein_coding | 1/18 | chrX | 70447385 | |||||||
| chrX:70447655 | T | G | 1 | a0001c0001t0001g0035 | 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 | a0001c0001t0001g0035 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.358-1257C>G | DLG3 | ENSG00000082458.12 | transcript | ENST00000374360.8 | protein_coding | 1/18 | chrX | 70447656 | |||||||
| chrX:70447965 | T | C | 17 | a0001c0001t0001g0037 a0001c0001t0001g0044 a0001c0001t0001g0045 others(14): 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:70448063 | A | C | 19 | a0001c0001t0001g0033 a0001c0001t0001g0037 a0001c0001t0001g0044 others(16): 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:70448203 | C | T | 3 | a0001c0001t0001g0177 a0001c0001t0001g0178 a0001c0001t0001g0215 |
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:70448299 | G | A | 17 | a0001c0001t0001g0033 a0001c0001t0001g0051 a0001c0001t0001g0053 others(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 | a0001c0001t0006g0176 | 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 | a0001c0001t0001g0060 | 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 | a0001c0001t0002g0061 a0001c0001t0002g0062 |
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:70448613 | A | G | 147 | a0001c0001t0001g0007 a0001c0001t0001g0022 a0001c0001t0001g0023 others(144): Show |
157 | HG00099.hp1 HG00621.hp1 HG00642.hp1 others(154): 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 | a0001c0001t0001g0129 | 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 | a0001c0001t0009g0050 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.358-165G>C | DLG3 | ENSG00000082458.12 | transcript | ENST00000374360.8 | protein_coding | 1/18 | chrX | 70448748 | |||||||
| chrX:70449022 | G | C | 1 | a0001c0001t0004g0179 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.408+59G>C | DLG3 | ENSG00000082458.12 | transcript | ENST00000374360.8 | protein_coding | 2/18 | chrX | 70449022 | |||||||
| chrX:70449143 | T | C | 1 | a0001c0001t0010g0021 | 2 | HG00733.hp1 NA20752.hp1 |
intron_variant | MODIFIER | c.408+180T>C | DLG3 | ENSG00000082458.12 | transcript | ENST00000374360.8 | protein_coding | 2/18 | chrX | 70449143 | |||||||
| chrX:70449596 | G | T | 1 | a0001c0001t0001g0217 | 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 | a0001c0001t0001g0217 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.534-92C>G | DLG3 | ENSG00000082458.12 | transcript | ENST00000374360.8 | protein_coding | 3/18 | chrX | 70449598 | |||||||
| chrX:70450331 | C | T | 3 | a0001c0001t0001g0175 a0001c0001t0008g0008 a0001c0001t0008g0174 |
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:70450427 | A | C | 1 | a0001c0001t0001g0033 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.840+122A>C | DLG3 | ENSG00000082458.12 | transcript | ENST00000374360.8 | protein_coding | 5/18 | chrX | 70450427 | |||||||
| chrX:70450462 | A | T | 19 | a0001c0001t0001g0051 a0001c0001t0001g0053 a0001c0001t0001g0054 others(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:70450981 | C | CATAGAGT others(11): Show |
1 | a0001c0001t0001g0182 | 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 | a0001c0001t0001g0051 a0001c0001t0001g0131 a0001c0001t0001g0132 |
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:70451115 | T | G | 1 | a0001c0001t0001g0030 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.985+332T>G | DLG3 | ENSG00000082458.12 | transcript | ENST00000374360.8 | protein_coding | 6/18 | chrX | 70451115 | |||||||
| chrX:70451208 | TCTC | T | 3 | a0001c0001t0009g0050 a0001c0001t0016g0059 a0001c0001t0019g0058 |
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 | a0001c0001t0001g0183 | 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 | a0001c0001t0001g0060 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.985+508C>T | DLG3 | ENSG00000082458.12 | transcript | ENST00000374360.8 | protein_coding | 6/18 | chrX | 70451291 | |||||||
| chrX:70451752 | A | G | 30 | a0001c0001t0001g0007 a0001c0001t0001g0022 a0001c0001t0001g0032 others(27): 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 | a0001c0001t0001g0028 a0001c0001t0001g0029 a0001c0001t0001g0221 others(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:70451850 | C | G | 1 | a0003c0003t0001g0170 | 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 | a0003c0003t0001g0170 | 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 | a0003c0003t0001g0170 | 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 | a0003c0003t0001g0170 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.986-11C>A | DLG3 | ENSG00000082458.12 | transcript | ENST00000374360.8 | protein_coding | 6/18 | chrX | 70451856 | |||||||
| chrX:70451861 | T | G | 1 | a0003c0003t0001g0170 | 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 | a0003c0003t0001g0170 | 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 | a0003c0003t0001g0170 | 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 | a0003c0003t0001g0170 | 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:70452331 | G | A | 1 | a0001c0001t0001g0184 | 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 | a0001c0001t0002g0020 | 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:70452612 | G | C | 96 | a0001c0001t0001g0007 a0001c0001t0001g0022 a0001c0001t0001g0023 others(93): Show |
104 | HG00621.hp1 HG00733.hp1 HG00735.hp1 others(101): 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 | a0001c0001t0002g0127 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.1145+715C>T | DLG3 | ENSG00000082458.12 | transcript | ENST00000374360.8 | protein_coding | 7/18 | chrX | 70452741 | |||||||
| chrX:70452805 | T | C | 150 | a0001c0001t0001g0007 a0001c0001t0001g0022 a0001c0001t0001g0023 others(147): Show |
161 | HG00099.hp1 HG00621.hp1 HG00642.hp1 others(158): 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 | a0001c0004t0002g0126 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.1146-791G>T | DLG3 | ENSG00000082458.12 | transcript | ENST00000374360.8 | protein_coding | 7/18 | chrX | 70452846 | |||||||
| chrX:70452971 | T | C | 1 | a0001c0001t0002g0068 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.1146-666T>C | DLG3 | ENSG00000082458.12 | transcript | ENST00000374360.8 | protein_coding | 7/18 | chrX | 70452971 | |||||||
| chrX:70453295 | G | A | 1 | a0001c0001t0001g0185 | 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 | a0001c0001t0001g0051 a0001c0001t0001g0053 a0001c0001t0001g0054 others(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:70453547 | C | T | 1 | a0001c0001t0002g0125 | 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 | 16 | a0001c0001t0001g0037 a0001c0001t0001g0044 a0001c0001t0001g0045 others(13): 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:70453867 | C | T | 1 | a0001c0001t0001g0140 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.1302+74C>T | DLG3 | ENSG00000082458.12 | transcript | ENST00000374360.8 | protein_coding | 8/18 | chrX | 70453867 | |||||||
| chrX:70453961 | T | C | 153 | a0001c0001t0001g0007 a0001c0001t0001g0022 a0001c0001t0001g0023 others(150): Show |
164 | HG00099.hp1 HG00621.hp1 HG00642.hp1 others(161): Show |
intron_variant | MODIFIER | c.1302+168T>C | DLG3 | ENSG00000082458.12 | transcript | ENST00000374360.8 | protein_coding | 8/18 | chrX | 70453961 | |||||||
| chrX:70454052 | T | G | 41 | a0001c0001t0001g0023 a0001c0001t0001g0026 a0001c0001t0001g0030 others(38): 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:70454655 | C | T | 1 | a0001c0001t0009g0050 | 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 | a0001c0002t0001g0046 a0001c0002t0001g0047 a0001c0002t0001g0048 others(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 | a0002c0005t0002g0069 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.1405+473C>A | DLG3 | ENSG00000082458.12 | transcript | ENST00000374360.8 | protein_coding | 9/18 | chrX | 70454789 | |||||||
| chrX:70455277 | G | T | 1 | a0001c0001t0015g0200 | 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 | a0001c0001t0002g0124 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.1405+978C>T | DLG3 | ENSG00000082458.12 | transcript | ENST00000374360.8 | protein_coding | 9/18 | chrX | 70455294 | |||||||
| chrX:70455330 | T | G | 1 | a0001c0001t0001g0033 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1405+1014T>G | DLG3 | ENSG00000082458.12 | transcript | ENST00000374360.8 | protein_coding | 9/18 | chrX | 70455330 | |||||||
| chrX:70455521 | G | T | 1 | a0001c0001t0014g0225 | 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 | a0001c0001t0009g0050 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.1405+1575G>C | DLG3 | ENSG00000082458.12 | transcript | ENST00000374360.8 | protein_coding | 9/18 | chrX | 70455891 | |||||||
| chrX:70456382 | G | A | 1 | a0001c0001t0001g0152 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.1405+2066G>A | DLG3 | ENSG00000082458.12 | transcript | ENST00000374360.8 | protein_coding | 9/18 | chrX | 70456382 | |||||||
| chrX:70456751 | CT | C | 14 | a0001c0001t0001g0037 a0001c0001t0001g0044 a0001c0001t0001g0045 others(11): 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 | a0001c0001t0002g0070 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.1405+2447T>C | DLG3 | ENSG00000082458.12 | transcript | ENST00000374360.8 | protein_coding | 9/18 | chrX | 70456763 | |||||||
| chrX:70456894 | C | T | 144 | a0001c0001t0001g0007 a0001c0001t0001g0022 a0001c0001t0001g0023 others(141): Show |
154 | HG00099.hp1 HG00621.hp1 HG00642.hp1 others(151): 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 | a0001c0001t0002g0019 a0001c0001t0002g0120 a0001c0001t0002g0121 others(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:70457106 | C | G | 88 | a0001c0001t0001g0007 a0001c0001t0001g0022 a0001c0001t0001g0023 others(85): Show |
96 | HG00621.hp1 HG00733.hp1 HG00735.hp1 others(93): 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 | a0001c0001t0001g0139 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1405+2919C>T | DLG3 | ENSG00000082458.12 | transcript | ENST00000374360.8 | protein_coding | 9/18 | chrX | 70457235 | |||||||
| chrX:70457546 | G | T | 1 | a0001c0001t0001g0241 | 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 | 41 | a0001c0001t0001g0023 a0001c0001t0001g0026 a0001c0001t0001g0030 others(38): 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:70457594 | C | T | 12 | a0001c0001t0001g0037 a0001c0001t0001g0044 a0001c0001t0001g0045 others(9): 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 | a0001c0001t0001g0033 | 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 | a0001c0001t0002g0068 | 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 | a0001c0001t0001g0033 | 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 | a0001c0001t0001g0055 a0001c0001t0001g0056 a0001c0001t0001g0057 |
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:70457916 | C | T | 7 | a0001c0001t0001g0051 a0001c0001t0001g0053 a0001c0001t0001g0054 others(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 | a0001c0001t0001g0030 a0001c0001t0001g0031 a0001c0001t0001g0142 others(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:70458292 | C | T | 12 | a0001c0001t0001g0037 a0001c0001t0001g0044 a0001c0001t0001g0045 others(9): 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 | a0001c0001t0001g0135 a0001c0001t0001g0233 a0001c0001t0001g0234 |
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 | 10 | a0001c0001t0001g0044 a0001c0001t0001g0045 a0001c0001t0003g0004 others(7): 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 | a0001c0001t0001g0224 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1405+4016C>T | DLG3 | ENSG00000082458.12 | transcript | ENST00000374360.8 | protein_coding | 9/18 | chrX | 70458332 | |||||||
| chrX:70458475 | A | G | 1 | a0001c0001t0001g0060 | 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 | 41 | a0001c0001t0001g0023 a0001c0001t0001g0026 a0001c0001t0001g0030 others(38): 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:70458883 | C | G | 5 | a0001c0001t0001g0029 a0001c0001t0001g0221 a0001c0001t0001g0223 others(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:70459047 | G | A | 1 | a0001c0001t0001g0184 | 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 | a0001c0001t0001g0154 | 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 | a0001c0001t0002g0071 a0001c0001t0002g0072 |
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:70459277 | A | G | 37 | a0001c0001t0001g0023 a0001c0001t0001g0026 a0001c0001t0001g0030 others(34): 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:70459357 | T | A | 147 | a0001c0001t0001g0007 a0001c0001t0001g0022 a0001c0001t0001g0023 others(144): Show |
157 | HG00099.hp1 HG00621.hp1 HG00642.hp1 others(154): Show |
intron_variant | MODIFIER | c.1405+5041T>A | DLG3 | ENSG00000082458.12 | transcript | ENST00000374360.8 | protein_coding | 9/18 | chrX | 70459357 | |||||||
| chrX:70459646 | G | A | 2 | a0001c0001t0016g0059 a0001c0001t0019g0058 |
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 | a0001c0001t0001g0235 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.1405+5737G>A | DLG3 | ENSG00000082458.12 | transcript | ENST00000374360.8 | protein_coding | 9/18 | chrX | 70460053 | |||||||
| chrX:70460282 | C | CA | 34 | a0001c0001t0002g0001 a0001c0001t0002g0010 a0001c0001t0002g0011 others(31): 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 | a0001c0001t0002g0005 a0001c0001t0002g0073 a0001c0001t0002g0074 others(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 | a0001c0001t0001g0030 a0001c0001t0001g0031 a0001c0001t0001g0134 others(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:70460284 | A | G | 1 | a0001c0001t0001g0033 | 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 | a0001c0001t0001g0037 a0001c0001t0001g0148 a0001c0001t0001g0149 others(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 | a0001c0001t0001g0032 a0001c0001t0001g0064 a0001c0001t0001g0129 others(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 | 119 | a0001c0001t0001g0007 a0001c0001t0001g0022 a0001c0001t0001g0023 others(116): Show |
129 | HG00099.hp1 HG00621.hp1 HG00733.hp1 others(126): Show |
intron_variant | MODIFIER | c.1405+5984A>C | DLG3 | ENSG00000082458.12 | transcript | ENST00000374360.8 | protein_coding | 9/18 | chrX | 70460300 | |||||||
| chrX:70460461 | A | T | 2 | a0001c0001t0016g0059 a0001c0001t0019g0058 |
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:70460551 | A | T | 13 | a0001c0001t0001g0030 a0001c0001t0001g0031 a0001c0001t0001g0142 others(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 | a0001c0001t0002g0119 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.1405+6246A>T | DLG3 | ENSG00000082458.12 | transcript | ENST00000374360.8 | protein_coding | 9/18 | chrX | 70460562 | |||||||
| chrX:70460715 | C | T | 1 | a0001c0001t0001g0241 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.1405+6399C>T | DLG3 | ENSG00000082458.12 | transcript | ENST00000374360.8 | protein_coding | 9/18 | chrX | 70460715 | |||||||
| chrX:70461212 | C | A | 1 | a0001c0001t0001g0143 | 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 | a0001c0001t0001g0143 | 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 | a0001c0001t0001g0143 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.1405+6898T>C | DLG3 | ENSG00000082458.12 | transcript | ENST00000374360.8 | protein_coding | 9/18 | chrX | 70461214 | |||||||
| chrX:70461447 | A | T | 1 | a0001c0001t0001g0057 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.1405+7131A>T | DLG3 | ENSG00000082458.12 | transcript | ENST00000374360.8 | protein_coding | 9/18 | chrX | 70461447 | |||||||
| chrX:70461499 | CG | C | 66 | a0001c0001t0001g0007 a0001c0001t0001g0022 a0001c0001t0001g0024 others(63): Show |
73 | HG00733.hp1 HG00735.hp1 HG01070.hp2 others(70): Show |
intron_variant | MODIFIER | c.1405+7189delG | DLG3 | ENSG00000082458.12 | transcript | ENST00000374360.8 | protein_coding | 9/18 | INFO_REALIGN_3_PRIME | chrX | 70461499 | ||||||
| chrX:70461574 | CT | C | 15 | a0001c0001t0001g0033 a0001c0001t0001g0037 a0001c0001t0001g0044 others(12): 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 | a0001c0001t0001g0051 a0001c0001t0001g0053 a0001c0001t0001g0054 others(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 | a0001c0001t0001g0216 | 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 | a0001c0002t0001g0046 a0001c0002t0001g0047 a0001c0002t0001g0048 others(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:70462026 | G | A | 23 | a0001c0001t0001g0051 a0001c0001t0001g0053 a0001c0001t0001g0054 others(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 | a0001c0001t0001g0029 a0001c0001t0001g0138 a0001c0001t0001g0167 others(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 | a0001c0001t0001g0026 a0001c0001t0001g0063 a0001c0001t0001g0064 others(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 | a0001c0001t0001g0030 a0001c0001t0001g0031 a0001c0001t0001g0146 others(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:70462046 | C | T | 7 | a0001c0001t0004g0118 a0001c0001t0004g0179 a0001c0001t0004g0219 others(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:70462243 | C | CT | 16 | a0001c0001t0002g0034 a0001c0001t0002g0062 a0001c0001t0002g0068 others(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 | CT | C | 115 | a0001c0001t0001g0007 a0001c0001t0001g0022 a0001c0001t0001g0024 others(112): Show |
123 | HG00621.hp1 HG00733.hp1 HG00735.hp1 others(120): 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 | 18 | a0001c0001t0001g0037 a0001c0001t0001g0044 a0001c0001t0001g0045 others(15): 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 | a0001c0001t0003g0166 | 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 | 25 | a0001c0001t0001g0007 a0001c0001t0001g0022 a0001c0001t0001g0032 others(22): 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 | a0003c0003t0001g0170 | 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 | a0001c0001t0001g0216 | 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 | a0001c0002t0001g0046 a0001c0002t0001g0047 a0001c0002t0001g0048 others(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: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 | a0001c0001t0001g0033 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1405+8237C>T | DLG3 | ENSG00000082458.12 | transcript | ENST00000374360.8 | protein_coding | 9/18 | chrX | 70462553 | |||||||
| chrX:70462817 | A | T | 150 | a0001c0001t0001g0007 a0001c0001t0001g0022 a0001c0001t0001g0023 others(147): Show |
161 | HG00099.hp1 HG00621.hp1 HG00642.hp1 others(158): 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 | a0001c0001t0014g0225 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.1405+8539T>G | DLG3 | ENSG00000082458.12 | transcript | ENST00000374360.8 | protein_coding | 9/18 | chrX | 70462855 | |||||||
| chrX:70462924 | T | C | 1 | a0001c0001t0001g0060 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.1405+8608T>C | DLG3 | ENSG00000082458.12 | transcript | ENST00000374360.8 | protein_coding | 9/18 | chrX | 70462924 | |||||||
| chrX:70463399 | G | A | 1 | a0001c0001t0001g0033 | 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 | 37 | a0001c0001t0001g0023 a0001c0001t0001g0026 a0001c0001t0001g0030 others(34): 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:70463538 | A | C | 1 | a0001c0001t0002g0114 | 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 | 15 | a0001c0001t0001g0033 a0001c0001t0001g0037 a0001c0001t0001g0044 others(12): 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 | a0001c0001t0002g0090 | 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 | a0001c0001t0002g0073 a0001c0001t0002g0079 a0001c0001t0002g0080 others(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 | a0001c0001t0002g0099 | 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 | TTTTCCTT others(3): Show |
T | 144 | a0001c0001t0001g0007 a0001c0001t0001g0022 a0001c0001t0001g0023 others(141): Show |
154 | HG00099.hp1 HG00621.hp1 HG00642.hp1 others(151): 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 | a0001c0001t0001g0037 a0001c0001t0001g0201 |
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 | a0001c0001t0001g0224 | 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 | a0001c0001t0005g0018 a0001c0001t0012g0018 |
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 | a0001c0001t0003g0036 | 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 | a0001c0001t0002g0101 | 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 | a0001c0001t0001g0228 | 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 | a0001c0001t0001g0226 a0001c0001t0001g0227 a0001c0001t0001g0228 |
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 | a0001c0001t0001g0216 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.1405+11358T>A | DLG3 | ENSG00000082458.12 | transcript | ENST00000374360.8 | protein_coding | 9/18 | chrX | 70465674 | |||||||
| chrX:70465905 | A | G | 13 | a0001c0001t0001g0037 a0001c0001t0001g0044 a0001c0001t0001g0045 others(10): 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 | 4 | a0001c0001t0003g0004 a0001c0001t0003g0036 a0001c0001t0003g0038 others(1): 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 | 66 | a0001c0001t0001g0007 a0001c0001t0001g0022 a0001c0001t0001g0024 others(63): Show |
73 | HG00733.hp1 HG00735.hp1 HG01070.hp2 others(70): Show |
intron_variant | MODIFIER | c.1405+11662C>T | DLG3 | ENSG00000082458.12 | transcript | ENST00000374360.8 | protein_coding | 9/18 | chrX | 70465978 | |||||||
| chrX:70466163 | G | A | 9 | a0001c0001t0003g0004 a0001c0001t0003g0036 a0001c0001t0003g0038 others(6): 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 | 27 | a0001c0001t0001g0007 a0001c0001t0001g0022 a0001c0001t0001g0032 others(24): 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 | a0001c0001t0001g0143 | 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 | TTG | 34 | a0001c0001t0001g0030 a0001c0001t0001g0172 a0001c0001t0001g0194 others(31): 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 | TTGTG | 15 | a0001c0001t0001g0056 a0001c0001t0001g0057 a0001c0001t0001g0228 others(12): 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 | TTG | T | 34 | a0001c0001t0001g0023 a0001c0001t0001g0026 a0001c0001t0001g0031 others(31): 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 | a0001c0001t0001g0139 a0001c0001t0001g0152 a0001c0001t0001g0191 others(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 | 21 | a0001c0001t0001g0028 a0001c0001t0001g0029 a0001c0001t0001g0033 others(18): 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 | 51 | a0001c0001t0001g0007 a0001c0001t0001g0022 a0001c0001t0001g0024 others(48): Show |
58 | HG00733.hp1 HG01070.hp2 HG01106.hp1 others(55): 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 | a0001c0001t0001g0037 a0001c0001t0001g0202 |
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 | a0001c0001t0001g0224 | 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 | a0001c0001t0001g0033 a0001c0001t0014g0225 |
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 | CT | C | 36 | a0001c0001t0001g0023 a0001c0001t0001g0026 a0001c0001t0001g0030 others(33): 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:70466629 | G | A | 66 | a0001c0001t0001g0007 a0001c0001t0001g0022 a0001c0001t0001g0024 others(63): Show |
73 | HG00733.hp1 HG00735.hp1 HG01070.hp2 others(70): 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 | a0001c0001t0001g0028 a0001c0001t0001g0029 a0001c0001t0001g0221 others(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:70467069 | A | G | 1 | a0001c0001t0001g0033 | 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 | a0001c0001t0005g0065 | 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 | a0001c0001t0016g0059 a0001c0001t0019g0058 |
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 | a0001c0001t0002g0088 | 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 | a0001c0002t0001g0046 a0001c0002t0001g0047 a0001c0002t0001g0048 others(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 | a0001c0001t0001g0051 a0001c0001t0001g0053 a0001c0001t0001g0054 others(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 | 152 | a0001c0001t0001g0007 a0001c0001t0001g0022 a0001c0001t0001g0023 others(149): Show |
163 | HG00099.hp1 HG00621.hp1 HG00642.hp1 others(160): 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 | a0001c0001t0001g0037 | 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 | a0001c0001t0001g0216 | 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 | a0001c0001t0004g0231 | 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 | a0001c0001t0014g0225 | 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 | 12 | a0001c0001t0001g0037 a0001c0001t0001g0044 a0001c0001t0001g0045 others(9): 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 | a0001c0001t0001g0033 a0001c0001t0014g0225 |
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 | 66 | a0001c0001t0001g0007 a0001c0001t0001g0022 a0001c0001t0001g0024 others(63): Show |
73 | HG00733.hp1 HG00735.hp1 HG01070.hp2 others(70): 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 | a0001c0001t0002g0097 a0001c0001t0002g0117 |
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:70469315 | A | G | 6 | a0001c0002t0001g0046 a0001c0002t0001g0047 a0001c0002t0001g0048 others(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:70469452 | T | C | 1 | a0001c0001t0002g0090 | 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 | a0001c0001t0010g0021 | 2 | HG00733.hp1 NA20752.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 | a0001c0001t0002g0034 | 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 | a0001c0001t0001g0155 | 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 | 113 | a0001c0001t0001g0007 a0001c0001t0001g0022 a0001c0001t0001g0023 others(110): Show |
121 | HG00621.hp1 HG00733.hp1 HG00735.hp1 others(118): 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 | a0001c0001t0001g0147 | 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 | a0001c0001t0001g0201 | 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 | a0001c0001t0009g0213 | 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 | a0001c0001t0001g0131 a0001c0001t0001g0132 |
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:70470566 | T | C | 2 | a0001c0001t0001g0203 a0001c0001t0001g0236 |
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 | 145 | a0001c0001t0001g0007 a0001c0001t0001g0022 a0001c0001t0001g0023 others(142): Show |
155 | HG00099.hp1 HG00621.hp1 HG00642.hp1 others(152): 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 | a0001c0001t0001g0053 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.1406-8331T>C | DLG3 | ENSG00000082458.12 | transcript | ENST00000374360.8 | protein_coding | 9/18 | chrX | 70470819 | |||||||
| chrX:70470864 | C | A | 20 | a0001c0001t0001g0030 a0001c0001t0001g0031 a0001c0001t0001g0142 others(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:70470980 | T | G | 2 | a0001c0001t0001g0140 a0001c0001t0001g0204 |
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 | a0001c0001t0013g0025 | 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 | a0001c0001t0001g0184 a0001c0001t0005g0141 |
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:70471078 | A | G | 23 | a0001c0001t0001g0051 a0001c0001t0001g0053 a0001c0001t0001g0054 others(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 | a0001c0001t0001g0028 a0001c0001t0001g0190 a0001c0001t0001g0198 others(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:70471403 | C | T | 1 | a0001c0001t0001g0037 | 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 | 66 | a0001c0001t0001g0007 a0001c0001t0001g0022 a0001c0001t0001g0024 others(63): Show |
73 | HG00733.hp1 HG00735.hp1 HG01070.hp2 others(70): 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 | a0001c0001t0009g0050 | 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 | 9 | a0001c0001t0002g0006 a0001c0001t0002g0015 a0001c0001t0002g0016 others(6): 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:70471772 | C | G | 1 | a0001c0001t0001g0037 | 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 | a0001c0001t0002g0014 a0001c0001t0002g0034 a0001c0001t0002g0111 |
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 | 13 | a0001c0001t0001g0033 a0001c0001t0001g0037 a0001c0001t0001g0044 others(10): 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 | 115 | a0001c0001t0001g0007 a0001c0001t0001g0022 a0001c0001t0001g0023 others(112): Show |
123 | HG00621.hp1 HG00733.hp1 HG00735.hp1 others(120): Show |
intron_variant | MODIFIER | c.1406-7042T>C | DLG3 | ENSG00000082458.12 | transcript | ENST00000374360.8 | protein_coding | 9/18 | chrX | 70472108 | |||||||
| chrX:70472381 | C | A | 1 | a0001c0001t0002g0076 | 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 | a0001c0001t0001g0164 a0001c0001t0001g0167 |
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 | a0001c0001t0001g0032 | 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 | a0001c0001t0010g0021 | 2 | HG00733.hp1 NA20752.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 | a0001c0001t0002g0114 | 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 | a0001c0002t0001g0046 a0001c0002t0001g0047 a0001c0002t0001g0048 others(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 | a0001c0001t0001g0140 a0001c0001t0001g0204 a0001c0001t0001g0214 |
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 | a0001c0001t0001g0030 a0001c0001t0001g0031 a0001c0001t0001g0044 others(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 | CA | C | 97 | a0001c0001t0001g0007 a0001c0001t0001g0022 a0001c0001t0001g0023 others(94): Show |
105 | HG00621.hp1 HG00733.hp1 HG00735.hp1 others(102): Show |
intron_variant | MODIFIER | c.1406-5972delA | DLG3 | ENSG00000082458.12 | transcript | ENST00000374360.8 | protein_coding | 9/18 | INFO_REALIGN_3_PRIME | chrX | 70473157 | ||||||
| chrX:70473403 | C | T | 2 | a0001c0001t0002g0012 a0001c0001t0002g0087 |
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 | 146 | a0001c0001t0001g0007 a0001c0001t0001g0022 a0001c0001t0001g0023 others(143): Show |
156 | HG00099.hp1 HG00621.hp1 HG00642.hp1 others(153): 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 | a0001c0001t0001g0184 | 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 | a0001c0001t0001g0030 a0001c0001t0001g0031 a0001c0001t0001g0142 others(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 | a0001c0001t0001g0033 | 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 | a0001c0001t0001g0051 a0001c0001t0001g0053 a0001c0001t0001g0054 others(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 | a0001c0001t0002g0114 | 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 | a0001c0001t0002g0114 | 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 | a0001c0001t0001g0148 a0001c0001t0001g0149 a0001c0001t0001g0150 |
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 | CA | C | 6 | a0001c0002t0001g0046 a0001c0002t0001g0047 a0001c0002t0001g0048 others(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 | 1 | a0001c0001t0002g0012 | 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 | a0001c0001t0001g0045 | 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 | a0001c0001t0001g0202 | 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 | a0001c0001t0001g0202 a0001c0001t0001g0238 |
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 | a0001c0001t0001g0044 | 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 | a0001c0001t0001g0131 a0001c0001t0001g0132 a0001c0001t0001g0164 others(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 | 9 | a0001c0001t0003g0004 a0001c0001t0003g0036 a0001c0001t0003g0038 others(6): 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 | a0001c0001t0016g0059 a0001c0001t0019g0058 |
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 | 27 | a0001c0001t0001g0007 a0001c0001t0001g0022 a0001c0001t0001g0032 others(24): 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 | a0001c0002t0001g0046 a0001c0002t0001g0047 a0001c0002t0001g0048 others(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 | a0001c0001t0001g0064 | 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 | a0001c0001t0001g0051 a0001c0001t0001g0053 a0001c0001t0001g0054 others(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 | a0001c0001t0001g0171 a0001c0001t0001g0172 |
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 | a0001c0001t0001g0135 a0001c0001t0001g0233 a0001c0001t0001g0234 |
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 | a0001c0001t0001g0037 | 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 | a0001c0001t0001g0027 | 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 | 146 | a0001c0001t0001g0007 a0001c0001t0001g0022 a0001c0001t0001g0023 others(143): Show |
156 | HG00099.hp1 HG00621.hp1 HG00642.hp1 others(153): 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 | a0001c0001t0014g0225 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.1406-795G>C | DLG3 | ENSG00000082458.12 | transcript | ENST00000374360.8 | protein_coding | 9/18 | chrX | 70478355 | |||||||
| chrX:70478613 | T | C | 1 | a0001c0001t0002g0061 | 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 | a0001c0001t0001g0139 | 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 | a0001c0001t0002g0017 a0001c0001t0002g0068 a0001c0001t0002g0093 others(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 | 146 | a0001c0001t0001g0007 a0001c0001t0001g0022 a0001c0001t0001g0023 others(143): Show |
156 | HG00099.hp1 HG00621.hp1 HG00642.hp1 others(153): 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 | a0001c0001t0002g0112 | 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 | a0001c0001t0001g0033 | 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 | a0001c0001t0001g0037 | 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 | a0001c0001t0002g0094 a0001c0001t0007g0091 |
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 | a0001c0001t0002g0094 a0001c0001t0007g0091 |
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 | a0001c0001t0001g0054 a0001c0001t0001g0139 a0001c0001t0001g0167 others(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 | a0001c0001t0001g0216 | 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 | a0001c0001t0009g0213 a0001c0001t0009g0240 |
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 | a0001c0001t0001g0171 a0001c0001t0001g0172 |
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 | a0001c0001t0001g0171 a0001c0001t0001g0172 |
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 | 148 | a0001c0001t0001g0007 a0001c0001t0001g0022 a0001c0001t0001g0023 others(145): Show |
158 | HG00099.hp1 HG00621.hp1 HG00642.hp1 others(155): 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 | a0001c0001t0001g0207 a0001c0001t0001g0212 |
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 | 25 | a0001c0001t0001g0023 a0001c0001t0001g0026 a0001c0001t0001g0063 others(22): 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 | 134 | a0001c0001t0001g0007 a0001c0001t0001g0022 a0001c0001t0001g0023 others(131): Show |
142 | HG00621.hp1 HG00733.hp1 HG00735.hp1 others(139): Show |
intron_variant | MODIFIER | c.1520+1194T>G | DLG3 | ENSG00000082458.12 | transcript | ENST00000374360.8 | protein_coding | 10/18 | chrX | 70480458 | |||||||
| chrX:70480540 | G | A | 147 | a0001c0001t0001g0007 a0001c0001t0001g0022 a0001c0001t0001g0023 others(144): Show |
157 | HG00099.hp1 HG00621.hp1 HG00642.hp1 others(154): Show |
intron_variant | MODIFIER | c.1520+1276G>A | DLG3 | ENSG00000082458.12 | transcript | ENST00000374360.8 | protein_coding | 10/18 | chrX | 70480540 | |||||||
| chrX:70480885 | G | A | 3 | a0001c0001t0001g0055 a0001c0001t0001g0056 a0001c0001t0001g0057 |
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 | a0001c0001t0002g0102 | 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 | a0001c0001t0004g0219 | 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 | a0001c0001t0002g0061 a0001c0001t0002g0062 a0001c0001t0002g0074 others(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 | 13 | a0001c0001t0001g0037 a0001c0001t0001g0044 a0001c0001t0001g0045 others(10): 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 | a0001c0001t0001g0055 | 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 | a0001c0001t0001g0027 | 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 | a0001c0001t0001g0134 a0001c0001t0001g0193 |
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 | a0001c0001t0001g0203 a0001c0001t0001g0208 |
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 | a0001c0001t0002g0020 | 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:70482408 | T | G | 1 | a0001c0001t0001g0064 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.1520+3144T>G | DLG3 | ENSG00000082458.12 | transcript | ENST00000374360.8 | protein_coding | 10/18 | chrX | 70482408 | |||||||
| chrX:70482660 | G | GTTTTT | 41 | a0001c0001t0001g0007 a0001c0001t0001g0026 a0001c0001t0001g0027 others(38): Show |
44 | HG00733.hp1 HG01070.hp2 HG01192.hp1 others(41): 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 | 33 | a0001c0001t0001g0023 a0001c0001t0001g0029 a0001c0001t0001g0032 others(30): 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 | a0001c0001t0001g0022 a0001c0001t0001g0152 a0001c0001t0001g0162 others(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 | T | 1 | a0001c0001t0001g0024 | 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:70482662 | G | GT | 10 | a0001c0001t0002g0011 a0001c0001t0002g0016 a0001c0001t0002g0079 others(7): 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 | GTTTTT | 13 | a0001c0001t0001g0051 a0001c0001t0001g0053 a0001c0001t0001g0055 others(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 | a0001c0001t0001g0054 a0001c0001t0001g0171 a0001c0001t0001g0216 others(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 | a0001c0001t0001g0045 | 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 |
4 | a0001c0001t0003g0004 a0001c0001t0003g0036 a0001c0001t0003g0041 others(1): 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 | a0001c0001t0001g0044 a0001c0001t0003g0039 a0001c0001t0003g0043 others(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 | a0001c0001t0003g0038 a0001c0001t0003g0040 |
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 | 87 | a0001c0001t0001g0007 a0001c0001t0001g0022 a0001c0001t0001g0023 others(84): Show |
95 | HG00621.hp1 HG00733.hp1 HG00735.hp1 others(92): 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 | a0001c0001t0001g0037 a0001c0001t0001g0145 a0001c0001t0001g0183 others(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 | a0001c0001t0001g0030 a0001c0001t0001g0031 a0001c0001t0001g0142 others(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 | a0001c0001t0002g0112 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.1520+3406T>G | DLG3 | ENSG00000082458.12 | transcript | ENST00000374360.8 | protein_coding | 10/18 | chrX | 70482670 | |||||||
| chrX:70482857 | C | T | 1 | a0001c0001t0001g0201 | 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 | 145 | a0001c0001t0001g0007 a0001c0001t0001g0022 a0001c0001t0001g0023 others(142): Show |
155 | HG00099.hp1 HG00621.hp1 HG00642.hp1 others(152): Show |
intron_variant | MODIFIER | c.1520+3660C>T | DLG3 | ENSG00000082458.12 | transcript | ENST00000374360.8 | protein_coding | 10/18 | chrX | 70482924 | |||||||
| chrX:70482926 | C | T | 145 | a0001c0001t0001g0007 a0001c0001t0001g0022 a0001c0001t0001g0023 others(142): Show |
155 | HG00099.hp1 HG00621.hp1 HG00642.hp1 others(152): 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 | a0001c0001t0003g0039 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.1520+3692C>T | DLG3 | ENSG00000082458.12 | transcript | ENST00000374360.8 | protein_coding | 10/18 | chrX | 70482956 | |||||||
| chrX:70483001 | C | G | 19 | a0001c0001t0001g0030 a0001c0001t0001g0031 a0001c0001t0001g0142 others(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 | a0001c0001t0002g0070 a0001c0001t0002g0119 a0001c0001t0005g0108 |
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 | 88 | a0001c0001t0001g0007 a0001c0001t0001g0022 a0001c0001t0001g0023 others(85): Show |
96 | HG00621.hp1 HG00733.hp1 HG00735.hp1 others(93): 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 | a0001c0001t0004g0220 | 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 | 145 | a0001c0001t0001g0007 a0001c0001t0001g0022 a0001c0001t0001g0023 others(142): Show |
155 | HG00099.hp1 HG00621.hp1 HG00642.hp1 others(152): 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 | a0001c0001t0002g0070 a0001c0001t0005g0108 |
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 | a0001c0001t0001g0033 a0001c0001t0001g0206 a0001c0001t0014g0225 |
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 | a0001c0001t0001g0129 | 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 | 88 | a0001c0001t0001g0007 a0001c0001t0001g0022 a0001c0001t0001g0023 others(85): Show |
96 | HG00621.hp1 HG00733.hp1 HG00735.hp1 others(93): Show |
intron_variant | MODIFIER | c.1520+5011C>T | DLG3 | ENSG00000082458.12 | transcript | ENST00000374360.8 | protein_coding | 10/18 | chrX | 70484275 | |||||||
| chrX:70484481 | T | G | 146 | a0001c0001t0001g0007 a0001c0001t0001g0022 a0001c0001t0001g0023 others(143): Show |
156 | HG00099.hp1 HG00621.hp1 HG00642.hp1 others(153): Show |
intron_variant | MODIFIER | c.1520+5217T>G | DLG3 | ENSG00000082458.12 | transcript | ENST00000374360.8 | protein_coding | 10/18 | chrX | 70484481 | |||||||
| chrX:70484521 | G | T | 145 | a0001c0001t0001g0007 a0001c0001t0001g0022 a0001c0001t0001g0023 others(142): Show |
155 | HG00099.hp1 HG00621.hp1 HG00642.hp1 others(152): 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 | a0001c0002t0001g0047 a0001c0002t0001g0048 |
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 | a0001c0001t0001g0033 | 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 | a0001c0001t0002g0061 | 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 | a0001c0001t0001g0143 | 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 | a0001c0001t0001g0157 | 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 | a0001c0001t0001g0175 | 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 | a0001c0001t0001g0206 | 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 | a0001c0001t0001g0024 a0001c0001t0001g0235 a0001c0001t0001g0237 |
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 | 145 | a0001c0001t0001g0007 a0001c0001t0001g0022 a0001c0001t0001g0023 others(142): Show |
155 | HG00099.hp1 HG00621.hp1 HG00642.hp1 others(152): 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 | a0001c0001t0001g0201 | 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 | 89 | a0001c0001t0001g0007 a0001c0001t0001g0022 a0001c0001t0001g0023 others(86): Show |
97 | HG00621.hp1 HG00733.hp1 HG00735.hp1 others(94): 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 | a0001c0001t0001g0033 | 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 | a0001c0001t0002g0079 | 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 | 71 | a0001c0001t0001g0007 a0001c0001t0001g0022 a0001c0001t0001g0030 others(68): Show |
77 | HG00733.hp1 HG00738.hp1 HG01081.hp2 others(74): Show |
intron_variant | MODIFIER | c.1521-5438dupT | DLG3 | ENSG00000082458.12 | transcript | ENST00000374360.8 | protein_coding | 10/18 | INFO_REALIGN_3_PRIME | chrX | 70486650 | ||||||
| chrX:70486669 | T | TTC | 13 | a0001c0001t0001g0037 a0001c0001t0001g0044 a0001c0001t0001g0045 others(10): 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 | a0001c0001t0018g0137 | 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 | a0001c0001t0019g0058 | 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 | a0001c0001t0001g0208 | 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 | a0001c0002t0001g0046 a0001c0002t0001g0047 a0001c0002t0001g0048 others(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 | 146 | a0001c0001t0001g0007 a0001c0001t0001g0022 a0001c0001t0001g0023 others(143): Show |
156 | HG00099.hp1 HG00621.hp1 HG00642.hp1 others(153): 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 | a0001c0001t0001g0033 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1521-4794C>T | DLG3 | ENSG00000082458.12 | transcript | ENST00000374360.8 | protein_coding | 10/18 | chrX | 70487313 | |||||||
| chrX:70487535 | T | C | 16 | a0001c0001t0001g0051 a0001c0001t0001g0053 a0001c0001t0001g0054 others(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 | 241 | a0001c0001t0001g0007 a0001c0001t0001g0022 a0001c0001t0001g0023 others(238): Show |
271 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(268): 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 | a0001c0001t0001g0204 | 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 | a0001c0001t0011g0116 | 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 | a0001c0001t0001g0053 | 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 | a0001c0001t0001g0033 | 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 | a0001c0001t0002g0070 a0001c0001t0002g0119 a0001c0001t0005g0108 |
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 | a0001c0001t0001g0208 | 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 | a0001c0001t0002g0066 a0001c0001t0005g0065 a0001c0001t0007g0067 |
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 | 146 | a0001c0001t0001g0007 a0001c0001t0001g0022 a0001c0001t0001g0023 others(143): Show |
156 | HG00099.hp1 HG00621.hp1 HG00642.hp1 others(153): 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 | a0001c0001t0002g0077 | 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 | a0001c0001t0002g0088 | 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 | 147 | a0001c0001t0001g0007 a0001c0001t0001g0022 a0001c0001t0001g0023 others(144): Show |
157 | HG00099.hp1 HG00621.hp1 HG00642.hp1 others(154): Show |
intron_variant | MODIFIER | c.1521-2988G>A | DLG3 | ENSG00000082458.12 | transcript | ENST00000374360.8 | protein_coding | 10/18 | chrX | 70489119 | |||||||
| chrX:70489391 | C | A | 1 | a0001c0001t0001g0216 | 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 | a0001c0001t0002g0090 | 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 | a0001c0001t0001g0051 a0001c0001t0001g0053 a0001c0001t0001g0054 others(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 | a0001c0001t0002g0218 | 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 | a0001c0001t0001g0224 | 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 | a0001c0001t0001g0208 | 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 | a0001c0002t0001g0046 a0001c0002t0001g0047 a0001c0002t0001g0048 others(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 | a0001c0001t0007g0091 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.1521-1797G>A | DLG3 | ENSG00000082458.12 | transcript | ENST00000374360.8 | protein_coding | 10/18 | chrX | 70490310 | |||||||
| chrX:70490436 | C | T | 6 | a0001c0002t0001g0046 a0001c0002t0001g0047 a0001c0002t0001g0048 others(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:70490919 | C | CT | 7 | a0001c0001t0001g0145 a0001c0002t0001g0046 a0001c0002t0001g0047 others(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 | a0001c0001t0001g0229 | 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 | 9 | a0001c0001t0003g0004 a0001c0001t0003g0036 a0001c0001t0003g0038 others(6): 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 | 149 | a0001c0001t0001g0007 a0001c0001t0001g0022 a0001c0001t0001g0023 others(146): Show |
159 | HG00099.hp1 HG00621.hp1 HG00642.hp1 others(156): 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 | a0001c0001t0001g0022 a0001c0001t0001g0163 |
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 | a0001c0001t0001g0044 | 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 | 22 | a0001c0001t0001g0023 a0001c0001t0001g0026 a0001c0001t0001g0063 others(19): 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 | a0001c0001t0001g0028 a0001c0001t0001g0221 a0001c0001t0001g0223 others(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 | a0001c0001t0002g0125 | 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 | a0001c0001t0001g0139 | 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 | a0001c0001t0002g0103 | 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 | a0001c0001t0001g0149 a0001c0001t0001g0150 |
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 | a0001c0001t0001g0051 a0001c0001t0001g0053 a0001c0001t0001g0054 others(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 | a0001c0001t0009g0050 | 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 | a0001c0001t0001g0033 a0001c0001t0014g0225 |
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 | a0001c0001t0001g0201 | 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 | a0001c0001t0001g0033 a0001c0001t0001g0129 a0001c0001t0001g0136 others(14): Show |
18 | HG00733.hp1 HG01070.hp2 HG01106.hp1 others(15): Show |
intron_variant | MODIFIER | c.1774-913T>C | DLG3 | ENSG00000082458.12 | transcript | ENST00000374360.8 | protein_coding | 12/18 | chrX | 70494495 | |||||||
| chrX:70494634 | A | G | 11 | a0001c0001t0001g0044 a0001c0001t0001g0045 a0001c0001t0003g0004 others(8): 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 | a0001c0001t0002g0092 | 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 | a0001c0001t0016g0059 | 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 | a0001c0002t0001g0046 a0001c0002t0001g0047 a0001c0002t0001g0048 others(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 | a0001c0001t0001g0207 a0001c0001t0001g0212 a0001c0001t0001g0239 others(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 | a0001c0002t0001g0046 a0001c0002t0001g0047 a0001c0002t0001g0048 others(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 | a0001c0001t0001g0158 | 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 | a0001c0001t0002g0099 | 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 | a0001c0001t0001g0030 a0001c0001t0001g0031 a0001c0001t0001g0142 others(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 | a0001c0001t0001g0053 | 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 | a0001c0001t0001g0044 | 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 | a0001c0002t0001g0046 a0001c0002t0001g0047 a0001c0002t0001g0048 others(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 | a0001c0002t0001g0046 a0001c0002t0001g0047 a0001c0002t0001g0048 others(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 | 98 | a0001c0001t0001g0007 a0001c0001t0001g0022 a0001c0001t0001g0023 others(95): 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:70497951 | C | A | 2 | a0001c0001t0002g0071 a0001c0001t0002g0072 |
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 | a0001c0001t0001g0029 a0001c0001t0001g0033 a0001c0001t0001g0129 others(15): Show |
19 | HG00733.hp1 HG01070.hp2 HG01106.hp1 others(16): 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 | a0001c0001t0016g0059 a0001c0001t0019g0058 |
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:70498464 | C | T | 145 | a0001c0001t0001g0007 a0001c0001t0001g0022 a0001c0001t0001g0023 others(142): Show |
155 | HG00099.hp1 HG00621.hp1 HG00642.hp1 others(152): Show |
intron_variant | MODIFIER | c.1820-56C>T | DLG3 | ENSG00000082458.12 | transcript | ENST00000374360.8 | protein_coding | 13/18 | chrX | 70498464 | |||||||
| chrX:70498597 | T | C | 2 | a0001c0001t0002g0070 a0001c0001t0005g0108 |
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 | a0001c0002t0001g0046 a0001c0002t0001g0047 a0001c0002t0001g0048 others(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:70498683 | CTCAT | C | 145 | a0001c0001t0001g0007 a0001c0001t0001g0022 a0001c0001t0001g0023 others(142): Show |
155 | HG00099.hp1 HG00621.hp1 HG00642.hp1 others(152): 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:70498848 | G | A | 1 | a0001c0001t0018g0137 | 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 | a0001c0001t0001g0157 | 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 | a0001c0001t0003g0041 | 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 | a0001c0001t0001g0201 | 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 | a0001c0001t0002g0101 | 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 | 145 | a0001c0001t0001g0007 a0001c0001t0001g0022 a0001c0001t0001g0023 others(142): Show |
155 | HG00099.hp1 HG00621.hp1 HG00642.hp1 others(152): Show |
intron_variant | MODIFIER | c.1973-152C>T | DLG3 | ENSG00000082458.12 | transcript | ENST00000374360.8 | protein_coding | 15/18 | chrX | 70499725 | |||||||
| chrX:70500247 | A | C | 1 | a0001c0001t0001g0214 | 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 | 9 | a0001c0001t0003g0004 a0001c0001t0003g0036 a0001c0001t0003g0038 others(6): 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 | a0001c0001t0001g0157 | 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 | a0001c0001t0001g0138 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.2146-118G>C | DLG3 | ENSG00000082458.12 | transcript | ENST00000374360.8 | protein_coding | 16/18 | chrX | 70500353 | |||||||
| chrX:70500622 | C | T | 1 | a0001c0001t0009g0050 | 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 | a0001c0002t0001g0046 a0001c0002t0001g0047 a0001c0002t0001g0048 others(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 | a0001c0001t0002g0085 | 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 | a0001c0001t0001g0224 | 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 | a0001c0001t0002g0068 | 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 | a0001c0001t0001g0189 | 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 | CTGTGTGT others(1): Show |
8 | a0001c0001t0001g0026 a0001c0001t0001g0028 a0001c0001t0001g0172 others(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 | a0001c0001t0001g0146 a0001c0001t0001g0158 a0001c0001t0001g0214 |
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 |
53 | a0001c0001t0001g0007 a0001c0001t0001g0022 a0001c0001t0001g0023 others(50): 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 | a0001c0001t0001g0029 a0001c0001t0001g0035 a0001c0001t0001g0129 others(27): Show |
31 | HG00733.hp1 HG01070.hp2 HG01106.hp1 others(28): 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 | a0001c0001t0001g0143 a0001c0001t0001g0188 a0001c0001t0018g0137 |
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 | a0001c0001t0001g0147 | 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:70501413 | C | CTG | 4 | a0001c0001t0002g0016 a0001c0001t0002g0105 a0001c0001t0016g0059 others(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 | a0001c0001t0001g0044 | 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 | a0001c0001t0003g0043 | 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 | a0001c0001t0001g0045 a0001c0001t0003g0004 a0001c0001t0003g0036 others(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 | a0001c0001t0003g0004 a0001c0001t0003g0039 |
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 | a0001c0002t0001g0046 a0001c0002t0001g0047 a0001c0002t0001g0048 others(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 | a0001c0001t0001g0033 a0001c0001t0001g0135 a0001c0001t0001g0171 others(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 | a0001c0001t0001g0056 a0001c0001t0001g0057 a0001c0001t0001g0201 others(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 | a0001c0001t0001g0051 a0001c0001t0001g0053 a0001c0001t0001g0054 others(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 | a0001c0001t0006g0176 | 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 | a0001c0001t0001g0037 | 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 | 100 | a0001c0001t0001g0007 a0001c0001t0001g0022 a0001c0001t0001g0023 others(97): Show |
108 | HG00621.hp1 HG00733.hp1 HG00735.hp1 others(105): 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 | a0001c0001t0002g0093 | 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 | a0001c0002t0001g0046 a0001c0002t0001g0047 a0001c0002t0001g0048 others(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 | a0001c0001t0002g0127 | 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 | a0001c0001t0001g0205 a0001c0001t0001g0210 |
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 | a0001c0001t0001g0162 | 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 | a0002c0005t0002g0069 | 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 | a0001c0001t0002g0105 | 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 | a0001c0001t0004g0118 a0001c0001t0004g0219 a0001c0001t0004g0220 others(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 |