Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 6102 |
| ensemblid | ENSG00000102218.6 |
| hgncid | 10274 |
| symbol | RP2 |
| name | RP2 activator of ARL3 GTPase |
| refseq_nuc | NM_006915.3 |
| refseq_prot | NP_008846.2 |
| ensembl_nuc | ENST00000218340.4 |
| ensembl_prot | ENSP00000218340.3 |
| mane_status | MANE Select |
| chr | chrX |
| start | 46837043 |
| end | 46882358 |
| strand | + |
| ver | v1.2 |
| region | chrX:46837043-46882358 |
| region5000 | chrX:46832043-46887358 |
| regionname0 | RP2_chrX_46837043_46882358 |
| regionname5000 | RP2_chrX_46832043_46887358 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 350 | 270 | 75 | 45 | 115 | 10 | 23 | 88 | RP2_chrX_46832043_46887358 | RP2 | MGCFF others(345): Show |
chrX | 46832043 | 46887358 |
| a0002 | 0/0 | 350 | 2 | 0 | 0 | 0 | 1 | 1 | 0 | RP2_chrX_46832043_46887358 | RP2 | MGCFF others(345): Show |
chrX | 46832043 | 46887358 |
| a0003 | 0/0 | 350 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | RP2_chrX_46832043_46887358 | RP2 | MGCFF others(345): Show |
chrX | 46832043 | 46887358 |
| a0004 | 0/0 | 350 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | RP2_chrX_46832043_46887358 | RP2 | MGCFF others(345): Show |
chrX | 46832043 | 46887358 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 1050 | 269 | 74 | 45 | 115 | 10 | 23 | RP2_chrX_46832043_46887358 | RP2 | ATGGG others(1045): Show |
chrX | 46832043 | 46887358 | ||
| a0001c0003 | 0/0 | 1050 | 1 | 1 | 0 | 0 | 0 | 0 | RP2_chrX_46832043_46887358 | RP2 | ATGGG others(1045): Show |
chrX | 46832043 | 46887358 | ||
| a0002c0002 | 0/0 | 1050 | 2 | 0 | 0 | 0 | 1 | 1 | RP2_chrX_46832043_46887358 | RP2 | ATGGG others(1045): Show |
chrX | 46832043 | 46887358 | ||
| a0003c0005 | 0/0 | 1050 | 1 | 1 | 0 | 0 | 0 | 0 | RP2_chrX_46832043_46887358 | RP2 | ATGGG others(1045): Show |
chrX | 46832043 | 46887358 | ||
| a0004c0004 | 0/0 | 1050 | 1 | 0 | 0 | 1 | 0 | 0 | RP2_chrX_46832043_46887358 | RP2 | ATGGG others(1045): Show |
chrX | 46832043 | 46887358 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/1 | 3700 | 238 | 55 | 43 | 106 | 10 | 23 | RP2_chrX_46832043_46887358 | RP2 | ACACT others(3695): Show |
chrX | 46832043 | 46887358 |
| a0001c0001t0002 | 1/0 | 3700 | 16 | 10 | 0 | 5 | 0 | 0 | RP2_chrX_46832043_46887358 | RP2 | ACACT others(3695): Show |
chrX | 46832043 | 46887358 |
| a0001c0001t0003 | 0/0 | 3700 | 6 | 6 | 0 | 0 | 0 | 0 | RP2_chrX_46832043_46887358 | RP2 | ACACT others(3695): Show |
chrX | 46832043 | 46887358 |
| a0001c0001t0004 | 0/0 | 3703 | 3 | 2 | 0 | 1 | 0 | 0 | RP2_chrX_46832043_46887358 | RP2 | ACACT others(3698): Show |
chrX | 46832043 | 46887358 |
| a0001c0001t0005 | 0/0 | 3700 | 2 | 0 | 0 | 2 | 0 | 0 | RP2_chrX_46832043_46887358 | RP2 | ACACT others(3695): Show |
chrX | 46832043 | 46887358 |
| a0001c0001t0006 | 0/0 | 3700 | 1 | 0 | 1 | 0 | 0 | 0 | RP2_chrX_46832043_46887358 | RP2 | ACACT others(3695): Show |
chrX | 46832043 | 46887358 |
| a0001c0001t0007 | 0/0 | 3700 | 1 | 0 | 1 | 0 | 0 | 0 | RP2_chrX_46832043_46887358 | RP2 | ACACT others(3695): Show |
chrX | 46832043 | 46887358 |
| a0001c0001t0008 | 0/0 | 3700 | 1 | 0 | 0 | 1 | 0 | 0 | RP2_chrX_46832043_46887358 | RP2 | ACACT others(3695): Show |
chrX | 46832043 | 46887358 |
| a0001c0001t0009 | 0/0 | 3700 | 1 | 1 | 0 | 0 | 0 | 0 | RP2_chrX_46832043_46887358 | RP2 | ACACT others(3695): Show |
chrX | 46832043 | 46887358 |
| a0001c0003t0001 | 0/0 | 3700 | 1 | 1 | 0 | 0 | 0 | 0 | RP2_chrX_46832043_46887358 | RP2 | ACACT others(3695): Show |
chrX | 46832043 | 46887358 |
| a0002c0002t0001 | 0/0 | 3700 | 2 | 0 | 0 | 0 | 1 | 1 | RP2_chrX_46832043_46887358 | RP2 | ACACT others(3695): Show |
chrX | 46832043 | 46887358 |
| a0003c0005t0001 | 0/0 | 3700 | 1 | 1 | 0 | 0 | 0 | 0 | RP2_chrX_46832043_46887358 | RP2 | ACACT others(3695): Show |
chrX | 46832043 | 46887358 |
| a0004c0004t0001 | 0/0 | 3700 | 1 | 0 | 0 | 1 | 0 | 0 | RP2_chrX_46832043_46887358 | RP2 | ACACT others(3695): Show |
chrX | 46832043 | 46887358 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 0/0 | 8 | 0 | 2 | 6 | 0 | 0 | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
| a0001c0001t0001g0002 | 0/0 | 6 | 1 | 1 | 1 | 0 | 3 | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
| a0001c0001t0001g0003 | 0/0 | 5 | 0 | 1 | 3 | 1 | 0 | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
| a0001c0001t0001g0004 | 0/0 | 4 | 0 | 3 | 1 | 0 | 0 | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
| a0001c0001t0001g0005 | 0/0 | 4 | 0 | 2 | 2 | 0 | 0 | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
| a0001c0001t0001g0007 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
| a0001c0001t0001g0008 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
| a0001c0001t0001g0009 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
| a0001c0001t0001g0010 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
| a0001c0001t0001g0011 | 0/0 | 3 | 0 | 1 | 2 | 0 | 0 | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
| a0001c0001t0001g0012 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
| a0001c0001t0001g0014 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
| a0001c0001t0001g0015 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
| a0001c0001t0001g0016 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
| a0001c0001t0001g0017 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
| a0001c0001t0001g0018 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
| a0001c0001t0001g0019 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
| a0001c0001t0001g0020 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
| a0001c0001t0001g0021 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
| a0001c0001t0001g0022 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
| a0001c0001t0001g0023 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
| a0001c0001t0001g0024 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
| a0001c0001t0001g0025 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
| a0001c0001t0001g0026 | 0/0 | 2 | 0 | 0 | 0 | 1 | 1 | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
| a0001c0001t0001g0027 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
| a0001c0001t0001g0028 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
| a0001c0001t0001g0029 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
| a0001c0001t0001g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
| a0001c0001t0001g0031 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
| a0001c0001t0001g0032 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
| a0001c0001t0001g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
| a0001c0001t0001g0034 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
| a0001c0001t0001g0035 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
| a0001c0001t0001g0036 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
| a0001c0001t0001g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
| a0001c0001t0001g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
| a0001c0001t0001g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
| a0001c0001t0001g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
| a0001c0001t0001g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
| a0001c0001t0001g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
| a0001c0001t0001g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
| a0001c0001t0001g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
| a0001c0001t0001g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
| a0001c0001t0001g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
| a0001c0001t0001g0053 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
| a0001c0001t0001g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
| a0001c0001t0001g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
| a0001c0001t0001g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
| a0001c0001t0001g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
| a0001c0001t0001g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
| a0001c0001t0001g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
| a0001c0001t0001g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
| a0001c0001t0001g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
| a0001c0001t0001g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
| a0001c0001t0001g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
| a0001c0001t0001g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
| a0001c0001t0001g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
| a0001c0001t0001g0067 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
| a0001c0001t0001g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
| a0001c0001t0001g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
| a0001c0001t0001g0071 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
| a0001c0001t0001g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
| a0001c0001t0001g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
| a0001c0001t0001g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
| a0001c0001t0001g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
| a0001c0001t0001g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
| a0001c0001t0001g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
| a0001c0001t0001g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
| a0001c0001t0001g0086 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
| a0001c0001t0001g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
| a0001c0001t0001g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
| a0001c0001t0001g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
| a0001c0001t0001g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
| a0001c0001t0001g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
| a0001c0001t0001g0092 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
| a0001c0001t0001g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
| a0001c0001t0001g0094 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
| a0001c0001t0001g0095 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
| a0001c0001t0001g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
| a0001c0001t0001g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
| a0001c0001t0001g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
| a0001c0001t0001g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
| a0001c0001t0001g0100 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
| a0001c0001t0001g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
| a0001c0001t0001g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
| a0001c0001t0001g0103 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
| a0001c0001t0001g0104 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
| a0001c0001t0001g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
| a0001c0001t0001g0106 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
| a0001c0001t0001g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
| a0001c0001t0001g0108 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
| a0001c0001t0001g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
| a0001c0001t0001g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
| a0001c0001t0001g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
| a0001c0001t0001g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
| a0001c0001t0001g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
| a0001c0001t0001g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
| a0001c0001t0001g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
| a0001c0001t0001g0116 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
| a0001c0001t0001g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
| a0001c0001t0001g0119 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
| a0001c0001t0001g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
| a0001c0001t0001g0121 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
| a0001c0001t0001g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
| a0001c0001t0001g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
| a0001c0001t0001g0124 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
| a0001c0001t0001g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
| a0001c0001t0001g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
| a0001c0001t0001g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
| a0001c0001t0001g0129 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
| a0001c0001t0001g0130 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
| a0001c0001t0001g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
| a0001c0001t0001g0133 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
| a0001c0001t0001g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
| a0001c0001t0001g0135 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
| a0001c0001t0001g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
| a0001c0001t0001g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
| a0001c0001t0001g0140 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
| a0001c0001t0001g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
| a0001c0001t0001g0142 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
| a0001c0001t0001g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
| a0001c0001t0001g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
| a0001c0001t0001g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
| a0001c0001t0001g0146 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
| a0001c0001t0001g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
| a0001c0001t0001g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
| a0001c0001t0001g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
| a0001c0001t0001g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
| a0001c0001t0001g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
| a0001c0001t0001g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
| a0001c0001t0001g0156 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
| a0001c0001t0001g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
| a0001c0001t0001g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
| a0001c0001t0001g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
| a0001c0001t0001g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
| a0001c0001t0001g0161 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
| a0001c0001t0001g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
| a0001c0001t0001g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
| a0001c0001t0001g0164 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
| a0001c0001t0001g0165 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
| a0001c0001t0001g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
| a0001c0001t0001g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
| a0001c0001t0001g0168 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
| a0001c0001t0001g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
| a0001c0001t0001g0170 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
| a0001c0001t0001g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
| a0001c0001t0001g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
| a0001c0001t0001g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
| a0001c0001t0001g0176 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
| a0001c0001t0001g0177 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
| a0001c0001t0001g0178 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
| a0001c0001t0001g0179 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
| a0001c0001t0001g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
| a0001c0001t0001g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
| a0001c0001t0001g0182 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
| a0001c0001t0001g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
| a0001c0001t0001g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
| a0001c0001t0001g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
| a0001c0001t0001g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
| a0001c0001t0001g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
| a0001c0001t0001g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
| a0001c0001t0001g0189 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
| a0001c0001t0001g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
| a0001c0001t0001g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
| a0001c0001t0001g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
| a0001c0001t0001g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
| a0001c0001t0001g0194 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
| a0001c0001t0001g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
| a0001c0001t0001g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
| a0001c0001t0001g0197 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
| a0001c0001t0001g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
| a0001c0001t0001g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
| a0001c0001t0001g0201 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
| a0001c0001t0001g0202 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
| a0001c0001t0001g0203 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
| a0001c0001t0001g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
| a0001c0001t0001g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
| a0001c0001t0001g0206 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
| a0001c0001t0001g0207 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
| a0001c0001t0001g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
| a0001c0001t0001g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
| a0001c0001t0001g0210 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
| a0001c0001t0001g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
| a0001c0001t0001g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
| a0001c0001t0001g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
| a0001c0001t0001g0215 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
| a0001c0001t0002g0006 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
| a0001c0001t0002g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
| a0001c0001t0002g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
| a0001c0001t0002g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
| a0001c0001t0002g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
| a0001c0001t0002g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
| a0001c0001t0002g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
| a0001c0001t0002g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
| a0001c0001t0002g0085 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
| a0001c0001t0002g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
| a0001c0001t0002g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
| a0001c0001t0002g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
| a0001c0001t0002g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
| a0001c0001t0003g0013 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
| a0001c0001t0003g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
| a0001c0001t0003g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
| a0001c0001t0003g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
| a0001c0001t0003g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
| a0001c0001t0004g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
| a0001c0001t0004g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
| a0001c0001t0004g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
| a0001c0001t0005g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
| a0001c0001t0005g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
| a0001c0001t0006g0012 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
| a0001c0001t0007g0199 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
| a0001c0001t0008g0003 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
| a0001c0001t0009g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
| a0001c0003t0001g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
| a0002c0002t0001g0118 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
| a0002c0002t0001g0125 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
| a0003c0005t0001g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
| a0004c0004t0001g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0001 | g0032 | EUR | GBR | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
| HG00099 | hp2 | a0001 | c0001 | t0001 | g0168 | EUR | GBR | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
| HG00140 | hp1 | a0001 | c0001 | t0001 | g0203 | EUR | GBR | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
| HG00280 | hp1 | a0001 | c0001 | t0001 | g0164 | EUR | FIN | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
| HG00323 | hp1 | a0001 | c0001 | t0001 | g0017 | EUR | FIN | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
| HG00323 | hp2 | a0001 | c0001 | t0001 | g0003 | EUR | FIN | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
| HG00408 | hp1 | a0001 | c0001 | t0001 | g0028 | EAS | CHS | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
| HG00408 | hp2 | a0001 | c0001 | t0001 | g0096 | EAS | CHS | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
| HG00423 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
| HG00423 | hp2 | a0001 | c0001 | t0001 | g0028 | EAS | CHS | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
| HG00438 | hp1 | a0001 | c0001 | t0001 | g0192 | EAS | CHS | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
| HG00438 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | CHS | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
| HG00544 | hp1 | a0001 | c0001 | t0001 | g0190 | EAS | CHS | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
| HG00544 | hp2 | a0001 | c0001 | t0001 | g0087 | EAS | CHS | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
| HG00558 | hp1 | a0001 | c0001 | t0005 | g0174 | EAS | CHS | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
| HG00558 | hp2 | a0001 | c0001 | t0001 | g0212 | EAS | CHS | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
| HG00609 | hp1 | a0001 | c0001 | t0001 | g0186 | EAS | CHS | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
| HG00621 | hp1 | a0001 | c0001 | t0001 | g0089 | EAS | CHS | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
| HG00639 | hp1 | a0001 | c0001 | t0001 | g0189 | AMR | PUR | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
| HG00639 | hp2 | a0001 | c0001 | t0001 | g0005 | AMR | PUR | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
| HG00642 | hp1 | a0001 | c0001 | t0001 | g0022 | AMR | PUR | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
| HG00673 | hp1 | a0001 | c0001 | t0001 | g0010 | EAS | CHS | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
| HG00738 | hp1 | a0001 | c0001 | t0001 | g0067 | AMR | PUR | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
| HG00741 | hp1 | a0001 | c0001 | t0001 | g0215 | AMR | PUR | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
| HG00741 | hp2 | a0001 | c0001 | t0001 | g0130 | AMR | PUR | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
| HG01069 | hp1 | a0001 | c0001 | t0001 | g0004 | AMR | PUR | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
| HG01070 | hp1 | a0001 | c0001 | t0001 | g0129 | AMR | PUR | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
| HG01070 | hp2 | a0001 | c0001 | t0001 | g0012 | AMR | PUR | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
| HG01071 | hp1 | a0001 | c0001 | t0001 | g0012 | AMR | PUR | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
| HG01071 | hp2 | a0001 | c0001 | t0001 | g0004 | AMR | PUR | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
| HG01074 | hp1 | a0001 | c0001 | t0001 | g0003 | AMR | PUR | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
| HG01081 | hp1 | a0001 | c0001 | t0001 | g0005 | AMR | PUR | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
| HG01081 | hp2 | a0001 | c0001 | t0001 | g0014 | AMR | PUR | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
| HG01099 | hp1 | a0001 | c0001 | t0001 | g0020 | AMR | PUR | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
| HG01106 | hp1 | a0001 | c0001 | t0001 | g0092 | AMR | PUR | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
| HG01109 | hp1 | a0001 | c0001 | t0001 | g0197 | AMR | PUR | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
| HG01167 | hp1 | a0001 | c0001 | t0001 | g0029 | AMR | PUR | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
| HG01169 | hp1 | a0001 | c0001 | t0001 | g0029 | AMR | PUR | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
| HG01169 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
| HG01175 | hp1 | a0001 | c0001 | t0001 | g0011 | AMR | PUR | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
| HG01175 | hp2 | a0001 | c0001 | t0001 | g0022 | AMR | PUR | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
| HG01192 | hp1 | a0001 | c0001 | t0001 | g0142 | AMR | PUR | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
| HG01243 | hp1 | a0001 | c0001 | t0001 | g0053 | AMR | PUR | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
| HG01255 | hp1 | a0001 | c0001 | t0001 | g0065 | AMR | CLM | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
| HG01256 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
| HG01258 | hp1 | a0001 | c0001 | t0001 | g0206 | AMR | CLM | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
| HG01261 | hp1 | a0001 | c0001 | t0001 | g0210 | AMR | CLM | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
| HG01358 | hp1 | a0001 | c0001 | t0001 | g0095 | AMR | CLM | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
| HG01433 | hp1 | a0001 | c0001 | t0001 | g0201 | AMR | CLM | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
| HG01515 | hp1 | a0001 | c0001 | t0001 | g0071 | EUR | IBS | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
| HG01516 | hp1 | a0002 | c0002 | t0001 | g0125 | EUR | IBS | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
| HG01516 | hp2 | a0001 | c0001 | t0001 | g0026 | EUR | IBS | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
| HG01884 | hp1 | a0001 | c0001 | t0001 | g0002 | AFR | ACB | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
| HG01884 | hp2 | a0001 | c0001 | t0001 | g0163 | AFR | ACB | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
| HG01891 | hp1 | a0001 | c0001 | t0001 | g0078 | AFR | ACB | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
| HG01891 | hp2 | a0001 | c0001 | t0001 | g0055 | AFR | ACB | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
| HG01928 | hp1 | a0001 | c0001 | t0001 | g0207 | AMR | PEL | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
| HG01934 | hp1 | a0001 | c0001 | t0001 | g0156 | AMR | PEL | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
| HG01943 | hp1 | a0001 | c0001 | t0001 | g0161 | AMR | PEL | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
| HG01952 | hp1 | a0001 | c0001 | t0001 | g0124 | AMR | PEL | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
| HG01975 | hp1 | a0001 | c0001 | t0001 | g0178 | AMR | PEL | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
| HG01975 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | PEL | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
| HG01981 | hp1 | a0001 | c0001 | t0001 | g0179 | AMR | PEL | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
| HG01981 | hp2 | a0001 | c0001 | t0001 | g0019 | AMR | PEL | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
| HG01993 | hp1 | a0001 | c0001 | t0001 | g0177 | AMR | PEL | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
| HG01993 | hp2 | a0001 | c0001 | t0001 | g0004 | AMR | PEL | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
| HG02015 | hp1 | a0001 | c0001 | t0001 | g0157 | EAS | KHV | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
| HG02027 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | KHV | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
| HG02040 | hp1 | a0001 | c0001 | t0001 | g0010 | EAS | KHV | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
| HG02055 | hp1 | a0001 | c0001 | t0001 | g0070 | AFR | ACB | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
| HG02056 | hp1 | a0001 | c0001 | t0001 | g0143 | EAS | KHV | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
| HG02071 | hp1 | a0001 | c0001 | t0001 | g0122 | EAS | KHV | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
| HG02074 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | KHV | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
| HG02083 | hp1 | a0001 | c0001 | t0008 | g0003 | EAS | KHV | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
| HG02129 | hp1 | a0001 | c0001 | t0001 | g0134 | EAS | KHV | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
| HG02132 | hp1 | a0001 | c0001 | t0001 | g0105 | EAS | KHV | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
| HG02135 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
| HG02145 | hp1 | a0001 | c0001 | t0001 | g0052 | AFR | ACB | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
| HG02257 | hp1 | a0001 | c0001 | t0002 | g0080 | AFR | ACB | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
| HG02257 | hp2 | a0001 | c0001 | t0001 | g0191 | AFR | ACB | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
| HG02258 | hp1 | a0001 | c0001 | t0001 | g0043 | AFR | ACB | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
| HG02273 | hp1 | a0001 | c0001 | t0007 | g0199 | AMR | PEL | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
| HG02273 | hp2 | a0001 | c0001 | t0001 | g0100 | AMR | PEL | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
| HG02280 | hp1 | a0001 | c0001 | t0001 | g0050 | AFR | ACB | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
| HG02280 | hp2 | a0001 | c0003 | t0001 | g0044 | AFR | ACB | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
| HG02300 | hp1 | a0001 | c0001 | t0006 | g0012 | AMR | PEL | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
| HG02451 | hp1 | a0001 | c0001 | t0001 | g0088 | AFR | ACB | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
| HG02451 | hp2 | a0001 | c0001 | t0001 | g0076 | AFR | ACB | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
| HG02523 | hp1 | a0001 | c0001 | t0001 | g0117 | EAS | KHV | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
| HG02523 | hp2 | a0001 | c0001 | t0001 | g0008 | EAS | KHV | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
| HG02572 | hp1 | a0001 | c0001 | t0001 | g0090 | AFR | GWD | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
| HG02602 | hp1 | a0001 | c0001 | t0001 | g0104 | SAS | PJL | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
| HG02615 | hp1 | a0001 | c0001 | t0001 | g0141 | AFR | GWD | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
| HG02615 | hp2 | a0001 | c0001 | t0001 | g0120 | AFR | GWD | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
| HG02622 | hp1 | a0001 | c0001 | t0002 | g0083 | AFR | GWD | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
| HG02622 | hp2 | a0001 | c0001 | t0003 | g0041 | AFR | GWD | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
| HG02630 | hp1 | a0001 | c0001 | t0002 | g0079 | AFR | GWD | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
| HG02630 | hp2 | a0001 | c0001 | t0001 | g0056 | AFR | GWD | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
| HG02647 | hp1 | a0001 | c0001 | t0001 | g0037 | AFR | GWD | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
| HG02683 | hp1 | a0001 | c0001 | t0001 | g0146 | SAS | PJL | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
| HG02683 | hp2 | a0001 | c0001 | t0001 | g0170 | SAS | PJL | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
| HG02698 | hp1 | a0001 | c0001 | t0001 | g0119 | SAS | PJL | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
| HG02717 | hp1 | a0001 | c0001 | t0009 | g0058 | AFR | GWD | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
| HG02723 | hp1 | a0001 | c0001 | t0001 | g0025 | AFR | GWD | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
| HG02723 | hp2 | a0001 | c0001 | t0001 | g0016 | AFR | GWD | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
| HG02735 | hp1 | a0001 | c0001 | t0001 | g0035 | SAS | PJL | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
| HG02738 | hp1 | a0001 | c0001 | t0001 | g0176 | SAS | PJL | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
| HG02809 | hp1 | a0001 | c0001 | t0001 | g0015 | AFR | GWD | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
| HG02809 | hp2 | a0001 | c0001 | t0001 | g0153 | AFR | GWD | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
| HG02818 | hp1 | a0001 | c0001 | t0003 | g0013 | AFR | GWD | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
| HG02818 | hp2 | a0001 | c0001 | t0001 | g0064 | AFR | GWD | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
| HG02886 | hp1 | a0001 | c0001 | t0001 | g0018 | AFR | GWD | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
| HG02886 | hp2 | a0001 | c0001 | t0004 | g0139 | AFR | GWD | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
| HG02895 | hp1 | a0001 | c0001 | t0001 | g0063 | AFR | GWD | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
| HG02897 | hp1 | a0001 | c0001 | t0001 | g0062 | AFR | GWD | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
| HG02897 | hp2 | a0001 | c0001 | t0001 | g0162 | AFR | GWD | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
| HG02922 | hp1 | a0001 | c0001 | t0001 | g0015 | AFR | ESN | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
| HG02922 | hp2 | a0001 | c0001 | t0001 | g0073 | AFR | ESN | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
| HG02965 | hp1 | a0003 | c0005 | t0001 | g0131 | AFR | ESN | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
| HG02970 | hp1 | a0001 | c0001 | t0003 | g0040 | AFR | ESN | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
| HG02970 | hp2 | a0001 | c0001 | t0002 | g0151 | AFR | ESN | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
| HG02976 | hp1 | a0001 | c0001 | t0001 | g0123 | AFR | ESN | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
| HG02976 | hp2 | a0001 | c0001 | t0001 | g0208 | AFR | ESN | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
| HG03017 | hp1 | a0002 | c0002 | t0001 | g0118 | SAS | PJL | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
| HG03041 | hp1 | a0001 | c0001 | t0002 | g0072 | AFR | GWD | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
| HG03041 | hp2 | a0001 | c0001 | t0002 | g0150 | AFR | GWD | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
| HG03098 | hp1 | a0001 | c0001 | t0002 | g0137 | AFR | MSL | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
| HG03130 | hp1 | a0001 | c0001 | t0001 | g0077 | AFR | ESN | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
| HG03139 | hp1 | a0001 | c0001 | t0001 | g0016 | AFR | ESN | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
| HG03195 | hp1 | a0001 | c0001 | t0001 | g0051 | AFR | ESN | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
| HG03195 | hp2 | a0001 | c0001 | t0001 | g0075 | AFR | ESN | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
| HG03209 | hp1 | a0001 | c0001 | t0003 | g0046 | AFR | MSL | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
| HG03225 | hp1 | a0001 | c0001 | t0003 | g0013 | AFR | MSL | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
| HG03453 | hp1 | a0001 | c0001 | t0002 | g0082 | AFR | MSL | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
| HG03453 | hp2 | a0001 | c0001 | t0001 | g0061 | AFR | MSL | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
| HG03490 | hp1 | a0001 | c0001 | t0001 | g0165 | SAS | PJL | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
| HG03492 | hp1 | a0001 | c0001 | t0001 | g0135 | SAS | PJL | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
| HG03516 | hp1 | a0001 | c0001 | t0001 | g0049 | AFR | ESN | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
| HG03516 | hp2 | a0001 | c0001 | t0001 | g0173 | AFR | ESN | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
| HG03540 | hp1 | a0001 | c0001 | t0001 | g0175 | AFR | GWD | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
| HG03540 | hp2 | a0001 | c0001 | t0001 | g0025 | AFR | GWD | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
| HG03579 | hp1 | a0001 | c0001 | t0001 | g0054 | AFR | MSL | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
| HG03654 | hp1 | a0001 | c0001 | t0001 | g0002 | SAS | PJL | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
| HG03669 | hp1 | a0001 | c0001 | t0001 | g0034 | SAS | PJL | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
| HG03669 | hp2 | a0001 | c0001 | t0001 | g0194 | SAS | PJL | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
| HG03688 | hp1 | a0001 | c0001 | t0001 | g0002 | SAS | STU | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
| HG03710 | hp1 | a0001 | c0001 | t0001 | g0133 | SAS | PJL | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
| HG03834 | hp1 | a0001 | c0001 | t0001 | g0026 | SAS | BEB | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
| HG03834 | hp2 | a0001 | c0001 | t0001 | g0002 | SAS | BEB | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
| HG03927 | hp1 | a0001 | c0001 | t0001 | g0036 | SAS | BEB | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
| HG03927 | hp2 | a0001 | c0001 | t0001 | g0106 | SAS | BEB | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
| HG03942 | hp1 | a0001 | c0001 | t0001 | g0121 | SAS | BEB | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
| HG04115 | hp1 | a0001 | c0001 | t0001 | g0094 | SAS | STU | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
| HG04199 | hp1 | a0001 | c0001 | t0001 | g0108 | SAS | STU | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
| HG04204 | hp1 | a0001 | c0001 | t0001 | g0116 | SAS | STU | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
| HG04228 | hp1 | a0001 | c0001 | t0001 | g0086 | SAS | STU | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
| NA18522 | hp1 | a0001 | c0001 | t0001 | g0023 | AFR | YRI | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
| NA18612 | hp1 | a0001 | c0001 | t0001 | g0145 | EAS | CHB | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
| NA18747 | hp1 | a0001 | c0001 | t0001 | g0205 | EAS | CHB | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
| NA18940 | hp1 | a0001 | c0001 | t0001 | g0099 | EAS | JPT | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
| NA18943 | hp1 | a0001 | c0001 | t0001 | g0126 | EAS | JPT | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
| NA18944 | hp1 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
| NA18945 | hp1 | a0001 | c0001 | t0002 | g0006 | EAS | JPT | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
| NA18948 | hp1 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
| NA18950 | hp1 | a0001 | c0001 | t0001 | g0019 | EAS | JPT | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
| NA18950 | hp2 | a0001 | c0001 | t0001 | g0183 | EAS | JPT | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
| NA18952 | hp1 | a0001 | c0001 | t0001 | g0093 | EAS | JPT | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
| NA18953 | hp1 | a0001 | c0001 | t0001 | g0160 | EAS | JPT | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
| NA18957 | hp1 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
| NA18957 | hp2 | a0001 | c0001 | t0002 | g0006 | EAS | JPT | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
| NA18959 | hp1 | a0001 | c0001 | t0001 | g0098 | EAS | JPT | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
| NA18960 | hp1 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
| NA18961 | hp1 | a0001 | c0001 | t0001 | g0091 | EAS | JPT | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
| NA18962 | hp1 | a0001 | c0001 | t0004 | g0211 | EAS | JPT | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
| NA18964 | hp1 | a0001 | c0001 | t0001 | g0101 | EAS | JPT | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
| NA18964 | hp2 | a0001 | c0001 | t0001 | g0169 | EAS | JPT | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
| NA18965 | hp1 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
| NA18966 | hp1 | a0001 | c0001 | t0001 | g0193 | EAS | JPT | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
| NA18967 | hp1 | a0001 | c0001 | t0001 | g0109 | EAS | JPT | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
| NA18968 | hp1 | a0001 | c0001 | t0001 | g0200 | EAS | JPT | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
| NA18968 | hp2 | a0001 | c0001 | t0001 | g0138 | EAS | JPT | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
| NA18970 | hp1 | a0001 | c0001 | t0001 | g0102 | EAS | JPT | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
| NA18971 | hp1 | a0004 | c0004 | t0001 | g0030 | EAS | JPT | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
| NA18972 | hp1 | a0001 | c0001 | t0001 | g0148 | EAS | JPT | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
| NA18972 | hp2 | a0001 | c0001 | t0001 | g0195 | EAS | JPT | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
| NA18973 | hp1 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
| NA18973 | hp2 | a0001 | c0001 | t0001 | g0181 | EAS | JPT | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
| NA18977 | hp1 | a0001 | c0001 | t0001 | g0144 | EAS | JPT | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
| NA18982 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
| NA18983 | hp1 | a0001 | c0001 | t0001 | g0027 | EAS | JPT | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
| NA18984 | hp1 | a0001 | c0001 | t0001 | g0024 | EAS | JPT | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
| NA18985 | hp1 | a0001 | c0001 | t0001 | g0198 | EAS | JPT | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
| NA18986 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
| NA18988 | hp1 | a0001 | c0001 | t0001 | g0107 | EAS | JPT | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
| NA18990 | hp1 | a0001 | c0001 | t0001 | g0112 | EAS | JPT | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
| NA18991 | hp1 | a0001 | c0001 | t0001 | g0214 | EAS | JPT | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
| NA18991 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
| NA18992 | hp1 | a0001 | c0001 | t0001 | g0158 | EAS | JPT | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
| NA18992 | hp2 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
| NA18993 | hp1 | a0001 | c0001 | t0001 | g0196 | EAS | JPT | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
| NA18993 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
| NA18994 | hp1 | a0001 | c0001 | t0001 | g0171 | EAS | JPT | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
| NA18995 | hp1 | a0001 | c0001 | t0001 | g0136 | EAS | JPT | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
| NA19000 | hp1 | a0001 | c0001 | t0005 | g0172 | EAS | JPT | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
| NA19001 | hp1 | a0001 | c0001 | t0001 | g0059 | EAS | JPT | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
| NA19001 | hp2 | a0001 | c0001 | t0001 | g0149 | EAS | JPT | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
| NA19004 | hp1 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
| NA19005 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
| NA19006 | hp1 | a0001 | c0001 | t0001 | g0021 | EAS | JPT | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
| NA19007 | hp1 | a0001 | c0001 | t0001 | g0030 | EAS | JPT | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
| NA19009 | hp1 | a0001 | c0001 | t0001 | g0187 | EAS | JPT | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
| NA19010 | hp1 | a0001 | c0001 | t0001 | g0084 | EAS | JPT | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
| NA19010 | hp2 | a0001 | c0001 | t0001 | g0166 | EAS | JPT | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
| NA19011 | hp1 | a0001 | c0001 | t0001 | g0113 | EAS | JPT | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
| NA19011 | hp2 | a0001 | c0001 | t0002 | g0069 | EAS | JPT | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
| NA19012 | hp1 | a0001 | c0001 | t0001 | g0188 | EAS | JPT | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
| NA19030 | hp1 | a0001 | c0001 | t0001 | g0057 | AFR | LWK | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
| NA19030 | hp2 | a0001 | c0001 | t0001 | g0154 | AFR | LWK | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
| NA19043 | hp1 | a0001 | c0001 | t0001 | g0048 | AFR | LWK | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
| NA19055 | hp1 | a0001 | c0001 | t0001 | g0045 | EAS | JPT | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
| NA19056 | hp1 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
| NA19057 | hp1 | a0001 | c0001 | t0001 | g0060 | EAS | JPT | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
| NA19057 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
| NA19058 | hp1 | a0001 | c0001 | t0001 | g0033 | EAS | JPT | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
| NA19060 | hp1 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
| NA19062 | hp1 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
| NA19064 | hp1 | a0001 | c0001 | t0001 | g0127 | EAS | JPT | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
| NA19064 | hp2 | a0001 | c0001 | t0001 | g0031 | EAS | JPT | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
| NA19065 | hp1 | a0001 | c0001 | t0001 | g0024 | EAS | JPT | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
| NA19065 | hp2 | a0001 | c0001 | t0001 | g0204 | EAS | JPT | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
| NA19066 | hp1 | a0001 | c0001 | t0002 | g0006 | EAS | JPT | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
| NA19067 | hp1 | a0001 | c0001 | t0001 | g0132 | EAS | JPT | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
| NA19068 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
| NA19070 | hp1 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
| NA19077 | hp1 | a0001 | c0001 | t0001 | g0114 | EAS | JPT | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
| NA19077 | hp2 | a0001 | c0001 | t0001 | g0180 | EAS | JPT | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
| NA19079 | hp1 | a0001 | c0001 | t0001 | g0097 | EAS | JPT | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
| NA19082 | hp1 | a0001 | c0001 | t0001 | g0167 | EAS | JPT | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
| NA19083 | hp1 | a0001 | c0001 | t0001 | g0128 | EAS | JPT | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
| NA19084 | hp1 | a0001 | c0001 | t0001 | g0147 | EAS | JPT | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
| NA19084 | hp2 | a0001 | c0001 | t0002 | g0006 | EAS | JPT | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
| NA19085 | hp1 | a0001 | c0001 | t0001 | g0027 | EAS | JPT | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
| NA19086 | hp1 | a0001 | c0001 | t0001 | g0213 | EAS | JPT | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
| NA19087 | hp1 | a0001 | c0001 | t0001 | g0110 | EAS | JPT | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
| NA19087 | hp2 | a0001 | c0001 | t0001 | g0184 | EAS | JPT | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
| NA19088 | hp1 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
| NA19089 | hp1 | a0001 | c0001 | t0001 | g0159 | EAS | JPT | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
| NA19090 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
| NA19090 | hp2 | a0001 | c0001 | t0001 | g0185 | EAS | JPT | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
| NA19091 | hp1 | a0001 | c0001 | t0001 | g0031 | EAS | JPT | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
| NA19240 | hp1 | a0001 | c0001 | t0001 | g0018 | AFR | YRI | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
| NA19240 | hp2 | a0001 | c0001 | t0003 | g0042 | AFR | YRI | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
| NA20129 | hp1 | a0001 | c0001 | t0001 | g0155 | AFR | ASW | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
| NA20129 | hp2 | a0001 | c0001 | t0001 | g0038 | AFR | ASW | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
| NA20752 | hp1 | a0001 | c0001 | t0001 | g0103 | EUR | TSI | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
| NA20805 | hp1 | a0001 | c0001 | t0001 | g0020 | EUR | TSI | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
| NA20905 | hp1 | a0001 | c0001 | t0001 | g0182 | SAS | GIH | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
| HG01123 | hp1 | a0001 | c0001 | t0001 | g0017 | AMR | CLM | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
| HG01123 | hp2 | a0001 | c0001 | t0001 | g0202 | AMR | CLM | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
| HG02109 | hp1 | a0001 | c0001 | t0001 | g0023 | AFR | ACB | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
| HG02109 | hp2 | a0001 | c0001 | t0002 | g0152 | AFR | ACB | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
| HG02486 | hp1 | a0001 | c0001 | t0004 | g0039 | AFR | ACB | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
| HG02559 | hp1 | a0001 | c0001 | t0001 | g0066 | AFR | ACB | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
| HG02559 | hp2 | a0001 | c0001 | t0001 | g0074 | AFR | ACB | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
| HG03471 | hp1 | a0001 | c0001 | t0002 | g0081 | AFR | MSL | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
| HG06807 | hp1 | a0001 | c0001 | t0001 | g0111 | AFR | USA | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
| HG06807 | hp2 | a0001 | c0001 | t0001 | g0014 | AFR | USA | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
| NA18955 | hp1 | a0001 | c0001 | t0001 | g0021 | EAS | JPT | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
| NA20300 | hp1 | a0001 | c0001 | t0001 | g0209 | AFR | USA | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
| NA20300 | hp2 | a0001 | c0001 | t0001 | g0047 | AFR | USA | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
| NA21309 | hp1 | a0001 | c0001 | t0001 | g0068 | AFR | LWK | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
| NA21309 | hp2 | a0001 | c0001 | t0001 | g0115 | AFR | LWK | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0001 | g0140 | REF | REF | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0002 | g0085 | REF | REF | RP2_chrX_46832043_46887358 | RP2 | chrX | 46832043 | 46887358 |
| 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:46853974 | A | G | 1 | a0003 | 1 | HG02965.hp1 | missense_variant | MODERATE | c.601A>G | p.Ile201Val | RP2 | ENSG00000102218.6 | transcript | ENST00000218340.4 | protein_coding | 2/5 | 659/3700 | 601/1053 | 201/350 | chrX | 46853974 | |||
| chrX:46860033 | A | G | 1 | a0004 | 1 | NA18971.hp1 | missense_variant | MODERATE | c.814A>G | p.Met272Val | RP2 | ENSG00000102218.6 | transcript | ENST00000218340.4 | protein_coding | 3/5 | 872/3700 | 814/1053 | 272/350 | chrX | 46860033 | |||
| chrX:46860063 | C | T | 1 | a0002 | 2 | HG01516.hp1 HG03017.hp1 |
missense_variant | MODERATE | c.844C>T | p.Arg282Trp | RP2 | ENSG00000102218.6 | transcript | ENST00000218340.4 | protein_coding | 3/5 | 902/3700 | 844/1053 | 282/350 | chrX | 46860063 |
| 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:46853979 | T | C | 1 | a0001c0003 | 1 | HG02280.hp2 | synonymous_variant | LOW | c.606T>C | p.Pro202Pro | RP2 | ENSG00000102218.6 | transcript | ENST00000218340.4 | protein_coding | 2/5 | 664/3700 | 606/1053 | 202/350 | chrX | 46853979 |
| 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:46880204 | C | T | 1 | a0001c0001t0009 | 1 | HG02717.hp1 | 3_prime_UTR_variant | MODIFIER | c.*435C>T | RP2 | ENSG00000102218.6 | transcript | ENST00000218340.4 | protein_coding | 5/5 | 435 | chrX | 46880204 | ||||||
| chrX:46880597 | G | A | 12 | a0001c0001t0001 a0001c0001t0003 a0001c0001t0004 others(9): Show |
257 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(254): Show |
3_prime_UTR_variant | MODIFIER | c.*828G>A | RP2 | ENSG00000102218.6 | transcript | ENST00000218340.4 | protein_coding | 5/5 | 828 | chrX | 46880597 | ||||||
| chrX:46880673 | A | G | 1 | a0001c0001t0008 | 1 | HG02083.hp1 | 3_prime_UTR_variant | MODIFIER | c.*904A>G | RP2 | ENSG00000102218.6 | transcript | ENST00000218340.4 | protein_coding | 5/5 | 904 | chrX | 46880673 | ||||||
| chrX:46880701 | A | G | 1 | a0001c0001t0007 | 1 | HG02273.hp1 | 3_prime_UTR_variant | MODIFIER | c.*932A>G | RP2 | ENSG00000102218.6 | transcript | ENST00000218340.4 | protein_coding | 5/5 | 932 | chrX | 46880701 | ||||||
| chrX:46881256 | C | A | 1 | a0001c0001t0006 | 1 | HG02300.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1487C>A | RP2 | ENSG00000102218.6 | transcript | ENST00000218340.4 | protein_coding | 5/5 | 1487 | chrX | 46881256 | ||||||
| chrX:46881463 | A | ATAT | 1 | a0001c0001t0004 | 3 | HG02486.hp1 HG02886.hp2 NA18962.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1717_*1719dupATT | RP2 | ENSG00000102218.6 | transcript | ENST00000218340.4 | protein_coding | 5/5 | 1720 | INFO_REALIGN_3_PRIME | chrX | 46881463 | |||||
| chrX:46881854 | T | C | 1 | a0001c0001t0003 | 6 | HG02622.hp2 HG02818.hp1 HG02970.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*2085T>C | RP2 | ENSG00000102218.6 | transcript | ENST00000218340.4 | protein_coding | 5/5 | 2085 | chrX | 46881854 | ||||||
| chrX:46881925 | A | G | 1 | a0001c0001t0005 | 2 | HG00558.hp1 NA19000.hp1 |
3_prime_UTR_variant | MODIFIER | c.*2156A>G | RP2 | ENSG00000102218.6 | transcript | ENST00000218340.4 | protein_coding | 5/5 | 2156 | chrX | 46881925 |
| 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:46837230 | C | T | 1 | a0001c0001t0001g0215 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.102+28C>T | RP2 | ENSG00000102218.6 | transcript | ENST00000218340.4 | protein_coding | 1/4 | chrX | 46837230 | |||||||
| chrX:46837258 | C | G | 1 | a0001c0001t0001g0214 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.102+56C>G | RP2 | ENSG00000102218.6 | transcript | ENST00000218340.4 | protein_coding | 1/4 | chrX | 46837258 | |||||||
| chrX:46837624 | G | A | 1 | a0001c0001t0001g0032 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.102+422G>A | RP2 | ENSG00000102218.6 | transcript | ENST00000218340.4 | protein_coding | 1/4 | chrX | 46837624 | |||||||
| chrX:46837667 | T | C | 1 | a0001c0001t0001g0033 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.102+465T>C | RP2 | ENSG00000102218.6 | transcript | ENST00000218340.4 | protein_coding | 1/4 | chrX | 46837667 | |||||||
| chrX:46837668 | C | T | 1 | a0001c0001t0001g0033 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.102+466C>T | RP2 | ENSG00000102218.6 | transcript | ENST00000218340.4 | protein_coding | 1/4 | chrX | 46837668 | |||||||
| chrX:46837669 | T | C | 1 | a0001c0001t0001g0033 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.102+467T>C | RP2 | ENSG00000102218.6 | transcript | ENST00000218340.4 | protein_coding | 1/4 | chrX | 46837669 | |||||||
| chrX:46837758 | G | A | 2 | a0001c0001t0001g0034 a0001c0001t0001g0035 |
2 | HG02735.hp1 HG03669.hp1 |
intron_variant | MODIFIER | c.102+556G>A | RP2 | ENSG00000102218.6 | transcript | ENST00000218340.4 | protein_coding | 1/4 | chrX | 46837758 | |||||||
| chrX:46837812 | G | T | 1 | a0001c0001t0001g0213 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.102+610G>T | RP2 | ENSG00000102218.6 | transcript | ENST00000218340.4 | protein_coding | 1/4 | chrX | 46837812 | |||||||
| chrX:46837984 | G | C | 1 | a0001c0001t0001g0036 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.102+782G>C | RP2 | ENSG00000102218.6 | transcript | ENST00000218340.4 | protein_coding | 1/4 | chrX | 46837984 | |||||||
| chrX:46838427 | A | G | 2 | a0001c0001t0001g0034 a0001c0001t0001g0035 |
2 | HG02735.hp1 HG03669.hp1 |
intron_variant | MODIFIER | c.102+1225A>G | RP2 | ENSG00000102218.6 | transcript | ENST00000218340.4 | protein_coding | 1/4 | chrX | 46838427 | |||||||
| chrX:46838560 | T | A | 1 | a0001c0001t0001g0033 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.102+1358T>A | RP2 | ENSG00000102218.6 | transcript | ENST00000218340.4 | protein_coding | 1/4 | chrX | 46838560 | |||||||
| chrX:46838957 | T | C | 3 | a0001c0001t0001g0037 a0001c0001t0001g0038 a0001c0001t0004g0039 |
3 | HG02486.hp1 HG02647.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.102+1755T>C | RP2 | ENSG00000102218.6 | transcript | ENST00000218340.4 | protein_coding | 1/4 | chrX | 46838957 | |||||||
| chrX:46839281 | G | T | 1 | a0001c0001t0001g0212 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.102+2079G>T | RP2 | ENSG00000102218.6 | transcript | ENST00000218340.4 | protein_coding | 1/4 | chrX | 46839281 | |||||||
| chrX:46839335 | T | G | 4 | a0001c0001t0003g0013 a0001c0001t0003g0040 a0001c0001t0003g0041 others(1): Show |
5 | HG02622.hp2 HG02818.hp1 HG02970.hp1 others(2): Show |
intron_variant | MODIFIER | c.102+2133T>G | RP2 | ENSG00000102218.6 | transcript | ENST00000218340.4 | protein_coding | 1/4 | chrX | 46839335 | |||||||
| chrX:46839507 | G | A | 1 | a0001c0001t0001g0043 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.102+2305G>A | RP2 | ENSG00000102218.6 | transcript | ENST00000218340.4 | protein_coding | 1/4 | chrX | 46839507 | |||||||
| chrX:46839561 | A | T | 81 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0010 others(78): Show |
99 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(96): Show |
intron_variant | MODIFIER | c.102+2359A>T | RP2 | ENSG00000102218.6 | transcript | ENST00000218340.4 | protein_coding | 1/4 | chrX | 46839561 | |||||||
| chrX:46839967 | G | T | 3 | a0001c0001t0001g0147 a0001c0001t0001g0148 a0001c0001t0001g0149 |
3 | NA18972.hp1 NA19001.hp2 NA19084.hp1 |
intron_variant | MODIFIER | c.102+2765G>T | RP2 | ENSG00000102218.6 | transcript | ENST00000218340.4 | protein_coding | 1/4 | chrX | 46839967 | |||||||
| chrX:46839993 | G | A | 1 | a0001c0003t0001g0044 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.102+2791G>A | RP2 | ENSG00000102218.6 | transcript | ENST00000218340.4 | protein_coding | 1/4 | chrX | 46839993 | |||||||
| chrX:46840151 | T | C | 1 | a0001c0001t0001g0045 | 1 | NA19055.hp1 | intron_variant | MODIFIER | c.102+2949T>C | RP2 | ENSG00000102218.6 | transcript | ENST00000218340.4 | protein_coding | 1/4 | chrX | 46840151 | |||||||
| chrX:46840199 | T | G | 1 | a0001c0001t0003g0046 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.102+2997T>G | RP2 | ENSG00000102218.6 | transcript | ENST00000218340.4 | protein_coding | 1/4 | chrX | 46840199 | |||||||
| chrX:46840368 | A | G | 72 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0010 others(69): Show |
89 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(86): Show |
intron_variant | MODIFIER | c.102+3166A>G | RP2 | ENSG00000102218.6 | transcript | ENST00000218340.4 | protein_coding | 1/4 | chrX | 46840368 | |||||||
| chrX:46840784 | T | G | 13 | a0001c0001t0001g0014 a0001c0001t0001g0047 a0001c0001t0001g0048 others(10): Show |
14 | HG01081.hp2 HG01243.hp1 HG01891.hp2 others(11): Show |
intron_variant | MODIFIER | c.102+3582T>G | RP2 | ENSG00000102218.6 | transcript | ENST00000218340.4 | protein_coding | 1/4 | chrX | 46840784 | |||||||
| chrX:46840889 | T | C | 1 | a0001c0001t0001g0157 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.102+3687T>C | RP2 | ENSG00000102218.6 | transcript | ENST00000218340.4 | protein_coding | 1/4 | chrX | 46840889 | |||||||
| chrX:46841237 | G | T | 1 | a0001c0001t0001g0146 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.102+4035G>T | RP2 | ENSG00000102218.6 | transcript | ENST00000218340.4 | protein_coding | 1/4 | chrX | 46841237 | |||||||
| chrX:46841424 | G | T | 1 | a0001c0001t0001g0145 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.102+4222G>T | RP2 | ENSG00000102218.6 | transcript | ENST00000218340.4 | protein_coding | 1/4 | chrX | 46841424 | |||||||
| chrX:46841425 | C | T | 1 | a0001c0001t0001g0145 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.102+4223C>T | RP2 | ENSG00000102218.6 | transcript | ENST00000218340.4 | protein_coding | 1/4 | chrX | 46841425 | |||||||
| chrX:46842146 | C | T | 6 | a0001c0001t0001g0025 a0001c0001t0001g0043 a0001c0001t0001g0153 others(3): Show |
7 | HG01934.hp1 HG02258.hp1 HG02723.hp1 others(4): Show |
intron_variant | MODIFIER | c.102+4944C>T | RP2 | ENSG00000102218.6 | transcript | ENST00000218340.4 | protein_coding | 1/4 | chrX | 46842146 | |||||||
| chrX:46842363 | A | G | 1 | a0001c0001t0004g0039 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.102+5161A>G | RP2 | ENSG00000102218.6 | transcript | ENST00000218340.4 | protein_coding | 1/4 | chrX | 46842363 | |||||||
| chrX:46842401 | A | G | 1 | a0001c0001t0004g0211 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.102+5199A>G | RP2 | ENSG00000102218.6 | transcript | ENST00000218340.4 | protein_coding | 1/4 | chrX | 46842401 | |||||||
| chrX:46842966 | G | A | 3 | a0001c0001t0001g0033 a0001c0001t0001g0059 a0001c0001t0001g0060 |
3 | NA19001.hp1 NA19057.hp1 NA19058.hp1 |
intron_variant | MODIFIER | c.102+5764G>A | RP2 | ENSG00000102218.6 | transcript | ENST00000218340.4 | protein_coding | 1/4 | chrX | 46842966 | |||||||
| chrX:46843005 | C | CT | 6 | a0001c0001t0001g0033 a0001c0001t0001g0142 a0001c0001t0001g0143 others(3): Show |
6 | HG01192.hp1 HG01261.hp1 HG02056.hp1 others(3): Show |
intron_variant | MODIFIER | c.102+5823dupT | RP2 | ENSG00000102218.6 | transcript | ENST00000218340.4 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chrX | 46843005 | ||||||
| chrX:46843005 | CT | C | 8 | a0001c0001t0001g0015 a0001c0001t0001g0016 a0001c0001t0001g0059 others(5): Show |
10 | HG02723.hp2 HG02809.hp1 HG02818.hp2 others(7): Show |
intron_variant | MODIFIER | c.102+5823delT | RP2 | ENSG00000102218.6 | transcript | ENST00000218340.4 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chrX | 46843005 | ||||||
| chrX:46843096 | C | T | 1 | a0001c0001t0001g0157 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.102+5894C>T | RP2 | ENSG00000102218.6 | transcript | ENST00000218340.4 | protein_coding | 1/4 | chrX | 46843096 | |||||||
| chrX:46843269 | A | T | 1 | a0001c0001t0001g0141 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.102+6067A>T | RP2 | ENSG00000102218.6 | transcript | ENST00000218340.4 | protein_coding | 1/4 | chrX | 46843269 | |||||||
| chrX:46843310 | G | C | 4 | a0001c0001t0001g0065 a0001c0001t0001g0066 a0001c0001t0001g0067 others(1): Show |
4 | HG00738.hp1 HG01255.hp1 HG02559.hp1 others(1): Show |
intron_variant | MODIFIER | c.102+6108G>C | RP2 | ENSG00000102218.6 | transcript | ENST00000218340.4 | protein_coding | 1/4 | chrX | 46843310 | |||||||
| chrX:46843453 | G | A | 2 | a0001c0001t0001g0034 a0001c0001t0001g0035 |
2 | HG02735.hp1 HG03669.hp1 |
intron_variant | MODIFIER | c.102+6251G>A | RP2 | ENSG00000102218.6 | transcript | ENST00000218340.4 | protein_coding | 1/4 | chrX | 46843453 | |||||||
| chrX:46843548 | C | A | 3 | a0001c0001t0001g0153 a0001c0001t0001g0154 a0001c0001t0001g0155 |
3 | HG02809.hp2 NA19030.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.102+6346C>A | RP2 | ENSG00000102218.6 | transcript | ENST00000218340.4 | protein_coding | 1/4 | chrX | 46843548 | |||||||
| chrX:46843925 | C | T | 2 | a0001c0001t0003g0046 a0001c0001t0004g0139 |
2 | HG02886.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.102+6723C>T | RP2 | ENSG00000102218.6 | transcript | ENST00000218340.4 | protein_coding | 1/4 | chrX | 46843925 | |||||||
| chrX:46844184 | A | T | 3 | a0001c0001t0001g0033 a0001c0001t0001g0059 a0001c0001t0001g0060 |
3 | NA19001.hp1 NA19057.hp1 NA19058.hp1 |
intron_variant | MODIFIER | c.102+6982A>T | RP2 | ENSG00000102218.6 | transcript | ENST00000218340.4 | protein_coding | 1/4 | chrX | 46844184 | |||||||
| chrX:46844409 | A | G | 13 | a0001c0001t0001g0014 a0001c0001t0001g0047 a0001c0001t0001g0048 others(10): Show |
14 | HG01081.hp2 HG01243.hp1 HG01891.hp2 others(11): Show |
intron_variant | MODIFIER | c.102+7207A>G | RP2 | ENSG00000102218.6 | transcript | ENST00000218340.4 | protein_coding | 1/4 | chrX | 46844409 | |||||||
| chrX:46844641 | A | G | 1 | a0001c0001t0004g0139 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.102+7439A>G | RP2 | ENSG00000102218.6 | transcript | ENST00000218340.4 | protein_coding | 1/4 | chrX | 46844641 | |||||||
| chrX:46844847 | C | G | 1 | a0001c0001t0004g0139 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.102+7645C>G | RP2 | ENSG00000102218.6 | transcript | ENST00000218340.4 | protein_coding | 1/4 | chrX | 46844847 | |||||||
| chrX:46845770 | G | GT | 5 | a0001c0001t0001g0138 a0001c0001t0001g0209 a0001c0001t0002g0150 others(2): Show |
5 | HG02109.hp2 HG02970.hp2 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.103-7695dupT | RP2 | ENSG00000102218.6 | transcript | ENST00000218340.4 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chrX | 46845770 | ||||||
| chrX:46845968 | G | A | 13 | a0001c0001t0001g0014 a0001c0001t0001g0047 a0001c0001t0001g0048 others(10): Show |
14 | HG01081.hp2 HG01243.hp1 HG01891.hp2 others(11): Show |
intron_variant | MODIFIER | c.103-7508G>A | RP2 | ENSG00000102218.6 | transcript | ENST00000218340.4 | protein_coding | 1/4 | chrX | 46845968 | |||||||
| chrX:46846009 | G | A | 1 | a0001c0001t0001g0159 | 1 | NA19089.hp1 | intron_variant | MODIFIER | c.103-7467G>A | RP2 | ENSG00000102218.6 | transcript | ENST00000218340.4 | protein_coding | 1/4 | chrX | 46846009 | |||||||
| chrX:46846828 | A | G | 1 | a0001c0001t0001g0045 | 1 | NA19055.hp1 | intron_variant | MODIFIER | c.103-6648A>G | RP2 | ENSG00000102218.6 | transcript | ENST00000218340.4 | protein_coding | 1/4 | chrX | 46846828 | |||||||
| chrX:46847025 | C | T | 1 | a0001c0001t0001g0208 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.103-6451C>T | RP2 | ENSG00000102218.6 | transcript | ENST00000218340.4 | protein_coding | 1/4 | chrX | 46847025 | |||||||
| chrX:46847493 | C | T | 1 | a0001c0001t0002g0137 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.103-5983C>T | RP2 | ENSG00000102218.6 | transcript | ENST00000218340.4 | protein_coding | 1/4 | chrX | 46847493 | |||||||
| chrX:46847497 | C | G | 2 | a0001c0001t0001g0007 a0001c0001t0001g0136 |
5 | NA18960.hp1 NA18992.hp2 NA18995.hp1 others(2): Show |
intron_variant | MODIFIER | c.103-5979C>G | RP2 | ENSG00000102218.6 | transcript | ENST00000218340.4 | protein_coding | 1/4 | chrX | 46847497 | |||||||
| chrX:46847630 | G | C | 1 | a0001c0001t0002g0069 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.103-5846G>C | RP2 | ENSG00000102218.6 | transcript | ENST00000218340.4 | protein_coding | 1/4 | chrX | 46847630 | |||||||
| chrX:46847668 | A | G | 1 | a0001c0001t0001g0068 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.103-5808A>G | RP2 | ENSG00000102218.6 | transcript | ENST00000218340.4 | protein_coding | 1/4 | chrX | 46847668 | |||||||
| chrX:46847687 | T | TATATATG others(21): Show |
1 | a0001c0001t0001g0024 | 2 | NA18984.hp1 NA19065.hp1 |
intron_variant | MODIFIER | c.103-5767_103-5740d others(30): Show |
RP2 | ENSG00000102218.6 | transcript | ENST00000218340.4 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chrX | 46847687 | ||||||
| chrX:46847704 | A | ATATACAC others(13): Show |
2 | a0001c0001t0001g0015 a0001c0001t0001g0070 |
3 | HG02055.hp1 HG02809.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.103-5768_103-5767i others(22): Show |
RP2 | ENSG00000102218.6 | transcript | ENST00000218340.4 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chrX | 46847704 | ||||||
| chrX:46847709 | T | C | 1 | a0001c0001t0003g0040 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.103-5767T>C | RP2 | ENSG00000102218.6 | transcript | ENST00000218340.4 | protein_coding | 1/4 | chrX | 46847709 | |||||||
| chrX:46847711 | C | T | 2 | a0001c0001t0001g0015 a0001c0001t0001g0070 |
3 | HG02055.hp1 HG02809.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.103-5765C>T | RP2 | ENSG00000102218.6 | transcript | ENST00000218340.4 | protein_coding | 1/4 | chrX | 46847711 | |||||||
| chrX:46847715 | CAT | C | 6 | a0001c0001t0001g0016 a0001c0001t0001g0061 a0001c0001t0001g0062 others(3): Show |
7 | HG02717.hp1 HG02723.hp2 HG02818.hp2 others(4): Show |
intron_variant | MODIFIER | c.103-5756_103-5755d others(4): Show |
RP2 | ENSG00000102218.6 | transcript | ENST00000218340.4 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chrX | 46847715 | ||||||
| chrX:46847716 | A | C | 3 | a0001c0001t0002g0150 a0001c0001t0002g0151 a0001c0001t0002g0152 |
3 | HG02109.hp2 HG02970.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.103-5760A>C | RP2 | ENSG00000102218.6 | transcript | ENST00000218340.4 | protein_coding | 1/4 | chrX | 46847716 | |||||||
| chrX:46847717 | T | C | 2 | a0001c0001t0001g0015 a0001c0001t0001g0070 |
3 | HG02055.hp1 HG02809.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.103-5759T>C | RP2 | ENSG00000102218.6 | transcript | ENST00000218340.4 | protein_coding | 1/4 | chrX | 46847717 | |||||||
| chrX:46847717 | T | TATATGTG others(15): Show |
2 | a0001c0001t0001g0175 a0001c0001t0001g0208 |
2 | HG02976.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.103-5747_103-5746i others(24): Show |
RP2 | ENSG00000102218.6 | transcript | ENST00000218340.4 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chrX | 46847717 | ||||||
| chrX:46847717 | T | TATATGTG others(17): Show |
25 | a0001c0001t0001g0008 a0001c0001t0001g0026 a0001c0001t0001g0027 others(22): Show |
31 | HG00099.hp2 HG00408.hp1 HG00423.hp2 others(28): Show |
intron_variant | MODIFIER | c.103-5732_103-5709d others(26): Show |
RP2 | ENSG00000102218.6 | transcript | ENST00000218340.4 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chrX | 46847717 | ||||||
| chrX:46847717 | T | TATATGTG others(41): Show |
2 | a0001c0001t0001g0037 a0001c0001t0001g0161 |
2 | HG01943.hp1 HG02647.hp1 |
intron_variant | MODIFIER | c.103-5756_103-5709d others(50): Show |
RP2 | ENSG00000102218.6 | transcript | ENST00000218340.4 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chrX | 46847717 | ||||||
| chrX:46847719 | T | TATGTGTG others(63): Show |
1 | a0001c0001t0001g0068 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.103-5709_103-5708i others(72): Show |
RP2 | ENSG00000102218.6 | transcript | ENST00000218340.4 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chrX | 46847719 | ||||||
| chrX:46847720 | ATG | A | 6 | a0001c0001t0001g0017 a0001c0001t0001g0071 a0001c0001t0003g0013 others(3): Show |
8 | HG00323.hp1 HG01123.hp1 HG01515.hp1 others(5): Show |
intron_variant | MODIFIER | c.103-5746_103-5745d others(4): Show |
RP2 | ENSG00000102218.6 | transcript | ENST00000218340.4 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chrX | 46847720 | ||||||
| chrX:46847721 | T | TGTGTGTG others(61): Show |
1 | a0001c0001t0001g0164 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.103-5709_103-5708i others(70): Show |
RP2 | ENSG00000102218.6 | transcript | ENST00000218340.4 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chrX | 46847721 | ||||||
| chrX:46847722 | G | GTGTGTGT others(13): Show |
4 | a0001c0001t0001g0029 a0001c0001t0001g0162 a0001c0001t0001g0163 others(1): Show |
5 | HG01167.hp1 HG01169.hp1 HG01884.hp2 others(2): Show |
intron_variant | MODIFIER | c.103-5747_103-5746i others(22): Show |
RP2 | ENSG00000102218.6 | transcript | ENST00000218340.4 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chrX | 46847722 | ||||||
| chrX:46847722 | G | GTGTGTGT others(13): Show |
1 | a0001c0001t0001g0158 | 1 | NA18992.hp1 | intron_variant | MODIFIER | c.103-5752_103-5733d others(22): Show |
RP2 | ENSG00000102218.6 | transcript | ENST00000218340.4 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chrX | 46847722 | ||||||
| chrX:46847722 | G | GTGTGTGT others(15): Show |
4 | a0001c0001t0001g0025 a0001c0001t0001g0043 a0001c0001t0001g0153 others(1): Show |
5 | HG02258.hp1 HG02723.hp1 HG02809.hp2 others(2): Show |
intron_variant | MODIFIER | c.103-5744_103-5723d others(24): Show |
RP2 | ENSG00000102218.6 | transcript | ENST00000218340.4 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chrX | 46847722 | ||||||
| chrX:46847733 | TATACACA others(39): Show |
T | 2 | a0001c0001t0002g0006 a0001c0001t0002g0069 |
5 | NA18945.hp1 NA18957.hp2 NA19011.hp2 others(2): Show |
intron_variant | MODIFIER | c.103-5732_103-5687d others(48): Show |
RP2 | ENSG00000102218.6 | transcript | ENST00000218340.4 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chrX | 46847733 | ||||||
| chrX:46847741 | CAT | C | 9 | a0001c0001t0001g0023 a0001c0001t0002g0072 a0001c0001t0002g0081 others(6): Show |
10 | HG02109.hp1 HG02622.hp2 HG02818.hp1 others(7): Show |
intron_variant | MODIFIER | c.103-5732_103-5731d others(4): Show |
RP2 | ENSG00000102218.6 | transcript | ENST00000218340.4 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chrX | 46847741 | ||||||
| chrX:46847742 | ATATG | A | 5 | a0001c0001t0002g0079 a0001c0001t0002g0080 a0001c0001t0002g0150 others(2): Show |
5 | HG02109.hp2 HG02257.hp1 HG02630.hp1 others(2): Show |
intron_variant | MODIFIER | c.103-5732_103-5729d others(6): Show |
RP2 | ENSG00000102218.6 | transcript | ENST00000218340.4 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chrX | 46847742 | ||||||
| chrX:46847743 | T | TGTGTGTG others(13): Show |
1 | a0001c0001t0002g0083 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.103-5733_103-5732i others(22): Show |
RP2 | ENSG00000102218.6 | transcript | ENST00000218340.4 | protein_coding | 1/4 | chrX | 46847743 | |||||||
| chrX:46847743 | TATGTGTG others(15): Show |
T | 1 | a0001c0001t0001g0120 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.103-5719_103-5698d others(24): Show |
RP2 | ENSG00000102218.6 | transcript | ENST00000218340.4 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chrX | 46847743 | ||||||
| chrX:46847744 | A | G | 5 | a0001c0001t0001g0049 a0001c0001t0001g0050 a0001c0001t0001g0051 others(2): Show |
5 | HG02145.hp1 HG02280.hp1 HG02717.hp1 others(2): Show |
intron_variant | MODIFIER | c.103-5732A>G | RP2 | ENSG00000102218.6 | transcript | ENST00000218340.4 | protein_coding | 1/4 | chrX | 46847744 | |||||||
| chrX:46847744 | ATGTGTGT others(17): Show |
A | 1 | a0001c0001t0001g0134 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.103-5722_103-5699d others(26): Show |
RP2 | ENSG00000102218.6 | transcript | ENST00000218340.4 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chrX | 46847744 | ||||||
| chrX:46847745 | T | TGTGTGTG others(33): Show |
1 | a0001c0001t0001g0155 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.103-5723_103-5722i others(42): Show |
RP2 | ENSG00000102218.6 | transcript | ENST00000218340.4 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chrX | 46847745 | ||||||
| chrX:46847745 | T | TGTGTGTG others(13): Show |
1 | a0001c0001t0001g0171 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.103-5730_103-5711d others(22): Show |
RP2 | ENSG00000102218.6 | transcript | ENST00000218340.4 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chrX | 46847745 | ||||||
| chrX:46847752 | G | A | 4 | a0001c0001t0001g0049 a0001c0001t0001g0050 a0001c0001t0001g0051 others(1): Show |
4 | HG02145.hp1 HG02280.hp1 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.103-5724G>A | RP2 | ENSG00000102218.6 | transcript | ENST00000218340.4 | protein_coding | 1/4 | chrX | 46847752 | |||||||
| chrX:46847754 | G | A | 4 | a0001c0001t0001g0049 a0001c0001t0001g0050 a0001c0001t0001g0051 others(1): Show |
4 | HG02145.hp1 HG02280.hp1 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.103-5722G>A | RP2 | ENSG00000102218.6 | transcript | ENST00000218340.4 | protein_coding | 1/4 | chrX | 46847754 | |||||||
| chrX:46847757 | TATACACA others(15): Show |
T | 1 | a0001c0001t0001g0143 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.103-5697_103-5676d others(24): Show |
RP2 | ENSG00000102218.6 | transcript | ENST00000218340.4 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chrX | 46847757 | ||||||
| chrX:46847758 | A | G | 1 | a0001c0001t0001g0002 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.103-5718A>G | RP2 | ENSG00000102218.6 | transcript | ENST00000218340.4 | protein_coding | 1/4 | chrX | 46847758 | |||||||
| chrX:46847765 | C | CAT | 4 | a0001c0001t0001g0031 a0001c0001t0001g0181 a0001c0001t0001g0186 others(1): Show |
4 | HG00609.hp1 NA18747.hp1 NA18973.hp2 others(1): Show |
intron_variant | MODIFIER | c.103-5710_103-5709d others(4): Show |
RP2 | ENSG00000102218.6 | transcript | ENST00000218340.4 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chrX | 46847765 | ||||||
| chrX:46847766 | A | G | 31 | a0001c0001t0001g0008 a0001c0001t0001g0025 a0001c0001t0001g0026 others(28): Show |
38 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(35): Show |
intron_variant | MODIFIER | c.103-5710A>G | RP2 | ENSG00000102218.6 | transcript | ENST00000218340.4 | protein_coding | 1/4 | chrX | 46847766 | |||||||
| chrX:46847767 | T | C | 1 | a0001c0001t0001g0001 | 1 | NA18993.hp2 | intron_variant | MODIFIER | c.103-5709T>C | RP2 | ENSG00000102218.6 | transcript | ENST00000218340.4 | protein_coding | 1/4 | chrX | 46847767 | |||||||
| chrX:46847767 | T | TATGTGTG others(13): Show |
1 | a0001c0001t0001g0180 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.103-5709_103-5708i others(22): Show |
RP2 | ENSG00000102218.6 | transcript | ENST00000218340.4 | protein_coding | 1/4 | chrX | 46847767 | |||||||
| chrX:46847767 | T | TATGTGTG others(15): Show |
25 | a0001c0001t0001g0003 a0001c0001t0001g0010 a0001c0001t0001g0011 others(22): Show |
33 | HG00323.hp2 HG00438.hp1 HG00438.hp2 others(30): Show |
intron_variant | MODIFIER | c.103-5709_103-5708i others(24): Show |
RP2 | ENSG00000102218.6 | transcript | ENST00000218340.4 | protein_coding | 1/4 | chrX | 46847767 | |||||||
| chrX:46847767 | T | TATGTGTG others(59): Show |
1 | a0001c0001t0001g0182 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.103-5709_103-5708i others(68): Show |
RP2 | ENSG00000102218.6 | transcript | ENST00000218340.4 | protein_coding | 1/4 | chrX | 46847767 | |||||||
| chrX:46847767 | T | TATGTGTG others(15): Show |
2 | a0001c0001t0001g0191 a0001c0001t0001g0197 |
2 | HG01109.hp1 HG02257.hp2 |
intron_variant | MODIFIER | c.103-5709_103-5708i others(24): Show |
RP2 | ENSG00000102218.6 | transcript | ENST00000218340.4 | protein_coding | 1/4 | chrX | 46847767 | |||||||
| chrX:46847767 | TGTGTGTG others(13): Show |
T | 13 | a0001c0001t0001g0030 a0001c0001t0001g0036 a0001c0001t0001g0049 others(10): Show |
14 | HG00140.hp1 HG02145.hp1 HG02280.hp1 others(11): Show |
intron_variant | MODIFIER | c.103-5708_103-5689d others(22): Show |
RP2 | ENSG00000102218.6 | transcript | ENST00000218340.4 | protein_coding | 1/4 | chrX | 46847767 | |||||||
| chrX:46847768 | G | A | 10 | a0001c0001t0001g0012 a0001c0001t0001g0031 a0001c0001t0001g0206 others(7): Show |
11 | HG01070.hp2 HG01071.hp1 HG01258.hp1 others(8): Show |
intron_variant | MODIFIER | c.103-5708G>A | RP2 | ENSG00000102218.6 | transcript | ENST00000218340.4 | protein_coding | 1/4 | chrX | 46847768 | |||||||
| chrX:46847770 | G | A | 3 | a0001c0001t0002g0150 a0001c0001t0002g0151 a0001c0001t0002g0152 |
3 | HG02109.hp2 HG02970.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.103-5706G>A | RP2 | ENSG00000102218.6 | transcript | ENST00000218340.4 | protein_coding | 1/4 | chrX | 46847770 | |||||||
| chrX:46847775 | TGTAC | T | 3 | a0001c0001t0002g0150 a0001c0001t0002g0151 a0001c0001t0002g0152 |
3 | HG02109.hp2 HG02970.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.103-5700_103-5697d others(6): Show |
RP2 | ENSG00000102218.6 | transcript | ENST00000218340.4 | protein_coding | 1/4 | chrX | 46847775 | |||||||
| chrX:46847776 | G | A | 38 | a0001c0001t0001g0008 a0001c0001t0001g0015 a0001c0001t0001g0016 others(35): Show |
47 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(44): Show |
intron_variant | MODIFIER | c.103-5700G>A | RP2 | ENSG00000102218.6 | transcript | ENST00000218340.4 | protein_coding | 1/4 | chrX | 46847776 | |||||||
| chrX:46847779 | C | T | 115 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0010 others(112): Show |
137 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(134): Show |
intron_variant | MODIFIER | c.103-5697C>T | RP2 | ENSG00000102218.6 | transcript | ENST00000218340.4 | protein_coding | 1/4 | chrX | 46847779 | |||||||
| chrX:46847781 | T | C | 38 | a0001c0001t0001g0008 a0001c0001t0001g0015 a0001c0001t0001g0016 others(35): Show |
47 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(44): Show |
intron_variant | MODIFIER | c.103-5695T>C | RP2 | ENSG00000102218.6 | transcript | ENST00000218340.4 | protein_coding | 1/4 | chrX | 46847781 | |||||||
| chrX:46847781 | T | TATATAC | 5 | a0001c0001t0001g0014 a0001c0001t0001g0054 a0001c0001t0001g0055 others(2): Show |
6 | HG01081.hp2 HG01891.hp2 HG02630.hp2 others(3): Show |
intron_variant | MODIFIER | c.103-5694_103-5693i others(8): Show |
RP2 | ENSG00000102218.6 | transcript | ENST00000218340.4 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chrX | 46847781 | ||||||
| chrX:46847783 | C | T | 3 | a0001c0001t0002g0150 a0001c0001t0002g0151 a0001c0001t0002g0152 |
3 | HG02109.hp2 HG02970.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.103-5693C>T | RP2 | ENSG00000102218.6 | transcript | ENST00000218340.4 | protein_coding | 1/4 | chrX | 46847783 | |||||||
| chrX:46847784 | A | G | 3 | a0001c0001t0002g0150 a0001c0001t0002g0151 a0001c0001t0002g0152 |
3 | HG02109.hp2 HG02970.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.103-5692A>G | RP2 | ENSG00000102218.6 | transcript | ENST00000218340.4 | protein_coding | 1/4 | chrX | 46847784 | |||||||
| chrX:46847785 | C | T | 3 | a0001c0001t0002g0150 a0001c0001t0002g0151 a0001c0001t0002g0152 |
3 | HG02109.hp2 HG02970.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.103-5691C>T | RP2 | ENSG00000102218.6 | transcript | ENST00000218340.4 | protein_coding | 1/4 | chrX | 46847785 | |||||||
| chrX:46847786 | A | G | 3 | a0001c0001t0002g0150 a0001c0001t0002g0151 a0001c0001t0002g0152 |
3 | HG02109.hp2 HG02970.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.103-5690A>G | RP2 | ENSG00000102218.6 | transcript | ENST00000218340.4 | protein_coding | 1/4 | chrX | 46847786 | |||||||
| chrX:46847787 | C | CAT | 44 | a0001c0001t0001g0003 a0001c0001t0001g0010 a0001c0001t0001g0011 others(41): Show |
52 | HG00323.hp2 HG00438.hp1 HG00438.hp2 others(49): Show |
intron_variant | MODIFIER | c.103-5688_103-5687d others(4): Show |
RP2 | ENSG00000102218.6 | transcript | ENST00000218340.4 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chrX | 46847787 | ||||||
| chrX:46847787 | C | CATATGTG others(41): Show |
1 | a0001c0001t0001g0181 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.103-5687_103-5686i others(50): Show |
RP2 | ENSG00000102218.6 | transcript | ENST00000218340.4 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chrX | 46847787 | ||||||
| chrX:46847787 | C | CGTGTGTG others(13): Show |
2 | a0001c0001t0001g0031 a0001c0001t0001g0205 |
3 | NA18747.hp1 NA19064.hp2 NA19091.hp1 |
intron_variant | MODIFIER | c.103-5689_103-5688i others(22): Show |
RP2 | ENSG00000102218.6 | transcript | ENST00000218340.4 | protein_coding | 1/4 | chrX | 46847787 | |||||||
| chrX:46847787 | C | CGTGTGTG others(15): Show |
6 | a0001c0001t0001g0012 a0001c0001t0001g0156 a0001c0001t0001g0207 others(3): Show |
7 | HG01070.hp2 HG01071.hp1 HG01261.hp1 others(4): Show |
intron_variant | MODIFIER | c.103-5689_103-5688i others(24): Show |
RP2 | ENSG00000102218.6 | transcript | ENST00000218340.4 | protein_coding | 1/4 | chrX | 46847787 | |||||||
| chrX:46847787 | C | T | 46 | a0001c0001t0001g0008 a0001c0001t0001g0014 a0001c0001t0001g0015 others(43): Show |
56 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(53): Show |
intron_variant | MODIFIER | c.103-5689C>T | RP2 | ENSG00000102218.6 | transcript | ENST00000218340.4 | protein_coding | 1/4 | chrX | 46847787 | |||||||
| chrX:46847788 | A | ATATATGT others(175): Show |
1 | a0001c0001t0001g0034 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.103-5687_103-5686i others(184): Show |
RP2 | ENSG00000102218.6 | transcript | ENST00000218340.4 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chrX | 46847788 | ||||||
| chrX:46847788 | A | ATATATGT others(173): Show |
1 | a0001c0001t0001g0035 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.103-5687_103-5686i others(182): Show |
RP2 | ENSG00000102218.6 | transcript | ENST00000218340.4 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chrX | 46847788 | ||||||
| chrX:46847788 | A | G | 1 | a0001c0001t0001g0206 | 1 | HG01258.hp1 | intron_variant | MODIFIER | c.103-5688A>G | RP2 | ENSG00000102218.6 | transcript | ENST00000218340.4 | protein_coding | 1/4 | chrX | 46847788 | |||||||
| chrX:46847790 | G | A | 12 | a0001c0001t0001g0018 a0001c0001t0001g0029 a0001c0001t0001g0034 others(9): Show |
14 | HG01167.hp1 HG01169.hp1 HG02109.hp2 others(11): Show |
intron_variant | MODIFIER | c.103-5686G>A | RP2 | ENSG00000102218.6 | transcript | ENST00000218340.4 | protein_coding | 1/4 | chrX | 46847790 | |||||||
| chrX:46847792 | G | A | 6 | a0001c0001t0001g0034 a0001c0001t0001g0035 a0001c0001t0002g0072 others(3): Show |
6 | HG02109.hp2 HG02735.hp1 HG02970.hp2 others(3): Show |
intron_variant | MODIFIER | c.103-5684G>A | RP2 | ENSG00000102218.6 | transcript | ENST00000218340.4 | protein_coding | 1/4 | chrX | 46847792 | |||||||
| chrX:46847794 | G | GTGTATAT others(19): Show |
1 | a0001c0001t0001g0206 | 1 | HG01258.hp1 | intron_variant | MODIFIER | c.103-5679_103-5678i others(28): Show |
RP2 | ENSG00000102218.6 | transcript | ENST00000218340.4 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chrX | 46847794 | ||||||
| chrX:46847798 | G | A | 1 | a0001c0001t0002g0072 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.103-5678G>A | RP2 | ENSG00000102218.6 | transcript | ENST00000218340.4 | protein_coding | 1/4 | chrX | 46847798 | |||||||
| chrX:46847802 | A | G | 1 | a0001c0001t0002g0072 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.103-5674A>G | RP2 | ENSG00000102218.6 | transcript | ENST00000218340.4 | protein_coding | 1/4 | chrX | 46847802 | |||||||
| chrX:46847804 | A | G | 1 | a0001c0001t0002g0072 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.103-5672A>G | RP2 | ENSG00000102218.6 | transcript | ENST00000218340.4 | protein_coding | 1/4 | chrX | 46847804 | |||||||
| chrX:46847806 | A | G | 3 | a0001c0001t0002g0150 a0001c0001t0002g0151 a0001c0001t0002g0152 |
3 | HG02109.hp2 HG02970.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.103-5670A>G | RP2 | ENSG00000102218.6 | transcript | ENST00000218340.4 | protein_coding | 1/4 | chrX | 46847806 | |||||||
| chrX:46847808 | A | G | 3 | a0001c0001t0002g0150 a0001c0001t0002g0151 a0001c0001t0002g0152 |
3 | HG02109.hp2 HG02970.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.103-5668A>G | RP2 | ENSG00000102218.6 | transcript | ENST00000218340.4 | protein_coding | 1/4 | chrX | 46847808 | |||||||
| chrX:46847809 | C | T | 3 | a0001c0001t0002g0150 a0001c0001t0002g0151 a0001c0001t0002g0152 |
3 | HG02109.hp2 HG02970.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.103-5667C>T | RP2 | ENSG00000102218.6 | transcript | ENST00000218340.4 | protein_coding | 1/4 | chrX | 46847809 | |||||||
| chrX:46847811 | C | T | 3 | a0001c0001t0002g0150 a0001c0001t0002g0151 a0001c0001t0002g0152 |
3 | HG02109.hp2 HG02970.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.103-5665C>T | RP2 | ENSG00000102218.6 | transcript | ENST00000218340.4 | protein_coding | 1/4 | chrX | 46847811 | |||||||
| chrX:46847813 | C | T | 4 | a0001c0001t0002g0072 a0001c0001t0002g0150 a0001c0001t0002g0151 others(1): Show |
4 | HG02109.hp2 HG02970.hp2 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.103-5663C>T | RP2 | ENSG00000102218.6 | transcript | ENST00000218340.4 | protein_coding | 1/4 | chrX | 46847813 | |||||||
| chrX:46847816 | A | G | 4 | a0001c0001t0002g0072 a0001c0001t0002g0150 a0001c0001t0002g0151 others(1): Show |
4 | HG02109.hp2 HG02970.hp2 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.103-5660A>G | RP2 | ENSG00000102218.6 | transcript | ENST00000218340.4 | protein_coding | 1/4 | chrX | 46847816 | |||||||
| chrX:46847818 | A | G | 4 | a0001c0001t0002g0072 a0001c0001t0002g0150 a0001c0001t0002g0151 others(1): Show |
4 | HG02109.hp2 HG02970.hp2 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.103-5658A>G | RP2 | ENSG00000102218.6 | transcript | ENST00000218340.4 | protein_coding | 1/4 | chrX | 46847818 | |||||||
| chrX:46847822 | G | A | 4 | a0001c0001t0002g0072 a0001c0001t0002g0150 a0001c0001t0002g0151 others(1): Show |
4 | HG02109.hp2 HG02970.hp2 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.103-5654G>A | RP2 | ENSG00000102218.6 | transcript | ENST00000218340.4 | protein_coding | 1/4 | chrX | 46847822 | |||||||
| chrX:46847822 | G | GTATATGT others(15): Show |
4 | a0001c0001t0002g0081 a0001c0001t0002g0082 a0001c0001t0002g0083 others(1): Show |
4 | HG02622.hp1 HG03098.hp1 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.103-5632_103-5611d others(24): Show |
RP2 | ENSG00000102218.6 | transcript | ENST00000218340.4 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chrX | 46847822 | ||||||
| chrX:46847822 | G | GTATATGT others(37): Show |
2 | a0001c0001t0002g0079 a0001c0001t0002g0080 |
2 | HG02257.hp1 HG02630.hp1 |
intron_variant | MODIFIER | c.103-5611_103-5610i others(46): Show |
RP2 | ENSG00000102218.6 | transcript | ENST00000218340.4 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chrX | 46847822 | ||||||
| chrX:46847824 | A | G | 1 | a0001c0001t0001g0053 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.103-5652A>G | RP2 | ENSG00000102218.6 | transcript | ENST00000218340.4 | protein_coding | 1/4 | chrX | 46847824 | |||||||
| chrX:46847826 | A | G | 1 | a0001c0001t0001g0053 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.103-5650A>G | RP2 | ENSG00000102218.6 | transcript | ENST00000218340.4 | protein_coding | 1/4 | chrX | 46847826 | |||||||
| chrX:46847901 | T | C | 4 | a0001c0001t0003g0013 a0001c0001t0003g0040 a0001c0001t0003g0041 others(1): Show |
5 | HG02622.hp2 HG02818.hp1 HG02970.hp1 others(2): Show |
intron_variant | MODIFIER | c.103-5575T>C | RP2 | ENSG00000102218.6 | transcript | ENST00000218340.4 | protein_coding | 1/4 | chrX | 46847901 | |||||||
| chrX:46847929 | CAT | C | 59 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0007 others(56): Show |
83 | HG00099.hp1 HG00323.hp1 HG00408.hp2 others(80): Show |
intron_variant | MODIFIER | c.103-5520_103-5519d others(4): Show |
RP2 | ENSG00000102218.6 | transcript | ENST00000218340.4 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chrX | 46847929 | ||||||
| chrX:46847929 | CATAT | C | 112 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0005 others(109): Show |
140 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(137): Show |
intron_variant | MODIFIER | c.103-5522_103-5519d others(6): Show |
RP2 | ENSG00000102218.6 | transcript | ENST00000218340.4 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chrX | 46847929 | ||||||
| chrX:46847929 | CATATAT | C | 29 | a0001c0001t0001g0011 a0001c0001t0001g0014 a0001c0001t0001g0047 others(26): Show |
32 | HG01081.hp2 HG01123.hp2 HG01175.hp1 others(29): Show |
intron_variant | MODIFIER | c.103-5524_103-5519d others(8): Show |
RP2 | ENSG00000102218.6 | transcript | ENST00000218340.4 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chrX | 46847929 | ||||||
| chrX:46848123 | C | G | 1 | a0001c0001t0001g0135 | 1 | HG03492.hp1 | intron_variant | MODIFIER | c.103-5353C>G | RP2 | ENSG00000102218.6 | transcript | ENST00000218340.4 | protein_coding | 1/4 | chrX | 46848123 | |||||||
| chrX:46848196 | C | G | 1 | a0001c0001t0009g0058 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.103-5280C>G | RP2 | ENSG00000102218.6 | transcript | ENST00000218340.4 | protein_coding | 1/4 | chrX | 46848196 | |||||||
| chrX:46848384 | A | AT | 9 | a0001c0001t0001g0034 a0001c0001t0001g0035 a0001c0001t0001g0036 others(6): Show |
9 | HG02055.hp1 HG02129.hp1 HG02145.hp1 others(6): Show |
intron_variant | MODIFIER | c.103-5075dupT | RP2 | ENSG00000102218.6 | transcript | ENST00000218340.4 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chrX | 46848384 | ||||||
| chrX:46848448 | G | A | 4 | a0001c0001t0003g0013 a0001c0001t0003g0040 a0001c0001t0003g0041 others(1): Show |
5 | HG02622.hp2 HG02818.hp1 HG02970.hp1 others(2): Show |
intron_variant | MODIFIER | c.103-5028G>A | RP2 | ENSG00000102218.6 | transcript | ENST00000218340.4 | protein_coding | 1/4 | chrX | 46848448 | |||||||
| chrX:46848454 | G | A | 1 | a0001c0001t0001g0090 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.103-5022G>A | RP2 | ENSG00000102218.6 | transcript | ENST00000218340.4 | protein_coding | 1/4 | chrX | 46848454 | |||||||
| chrX:46848519 | A | G | 184 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0005 others(181): Show |
228 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(225): Show |
intron_variant | MODIFIER | c.103-4957A>G | RP2 | ENSG00000102218.6 | transcript | ENST00000218340.4 | protein_coding | 1/4 | chrX | 46848519 | |||||||
| chrX:46848689 | C | T | 85 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0010 others(82): Show |
105 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(102): Show |
intron_variant | MODIFIER | c.103-4787C>T | RP2 | ENSG00000102218.6 | transcript | ENST00000218340.4 | protein_coding | 1/4 | chrX | 46848689 | |||||||
| chrX:46848734 | A | G | 1 | a0001c0001t0001g0104 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.103-4742A>G | RP2 | ENSG00000102218.6 | transcript | ENST00000218340.4 | protein_coding | 1/4 | chrX | 46848734 | |||||||
| chrX:46849039 | A | G | 4 | a0001c0001t0001g0065 a0001c0001t0001g0066 a0001c0001t0001g0067 others(1): Show |
4 | HG00738.hp1 HG01255.hp1 HG02559.hp1 others(1): Show |
intron_variant | MODIFIER | c.103-4437A>G | RP2 | ENSG00000102218.6 | transcript | ENST00000218340.4 | protein_coding | 1/4 | chrX | 46849039 | |||||||
| chrX:46849161 | C | T | 1 | a0001c0001t0001g0087 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.103-4315C>T | RP2 | ENSG00000102218.6 | transcript | ENST00000218340.4 | protein_coding | 1/4 | chrX | 46849161 | |||||||
| chrX:46849282 | C | T | 4 | a0001c0001t0001g0065 a0001c0001t0001g0066 a0001c0001t0001g0067 others(1): Show |
4 | HG00738.hp1 HG01255.hp1 HG02559.hp1 others(1): Show |
intron_variant | MODIFIER | c.103-4194C>T | RP2 | ENSG00000102218.6 | transcript | ENST00000218340.4 | protein_coding | 1/4 | chrX | 46849282 | |||||||
| chrX:46849377 | C | T | 1 | a0001c0001t0004g0139 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.103-4099C>T | RP2 | ENSG00000102218.6 | transcript | ENST00000218340.4 | protein_coding | 1/4 | chrX | 46849377 | |||||||
| chrX:46850049 | G | A | 1 | a0001c0001t0001g0153 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.103-3427G>A | RP2 | ENSG00000102218.6 | transcript | ENST00000218340.4 | protein_coding | 1/4 | chrX | 46850049 | |||||||
| chrX:46850691 | ATCCATTC others(13): Show |
A | 1 | a0001c0001t0001g0091 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.103-2784_103-2765d others(22): Show |
RP2 | ENSG00000102218.6 | transcript | ENST00000218340.4 | protein_coding | 1/4 | chrX | 46850691 | |||||||
| chrX:46851088 | AT | A | 10 | a0001c0001t0002g0072 a0001c0001t0002g0079 a0001c0001t0002g0080 others(7): Show |
10 | HG02109.hp2 HG02257.hp1 HG02622.hp1 others(7): Show |
intron_variant | MODIFIER | c.103-2385delT | RP2 | ENSG00000102218.6 | transcript | ENST00000218340.4 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chrX | 46851088 | ||||||
| chrX:46851386 | C | T | 99 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0010 others(96): Show |
120 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(117): Show |
intron_variant | MODIFIER | c.103-2090C>T | RP2 | ENSG00000102218.6 | transcript | ENST00000218340.4 | protein_coding | 1/4 | chrX | 46851386 | |||||||
| chrX:46851560 | C | T | 1 | a0001c0001t0001g0143 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.103-1916C>T | RP2 | ENSG00000102218.6 | transcript | ENST00000218340.4 | protein_coding | 1/4 | chrX | 46851560 | |||||||
| chrX:46851620 | G | A | 1 | a0001c0001t0004g0139 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.103-1856G>A | RP2 | ENSG00000102218.6 | transcript | ENST00000218340.4 | protein_coding | 1/4 | chrX | 46851620 | |||||||
| chrX:46851697 | C | T | 1 | a0001c0001t0003g0046 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.103-1779C>T | RP2 | ENSG00000102218.6 | transcript | ENST00000218340.4 | protein_coding | 1/4 | chrX | 46851697 | |||||||
| chrX:46851792 | C | T | 1 | a0001c0001t0001g0133 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.103-1684C>T | RP2 | ENSG00000102218.6 | transcript | ENST00000218340.4 | protein_coding | 1/4 | chrX | 46851792 | |||||||
| chrX:46851838 | G | A | 2 | a0001c0001t0001g0092 a0001c0001t0001g0142 |
2 | HG01106.hp1 HG01192.hp1 |
intron_variant | MODIFIER | c.103-1638G>A | RP2 | ENSG00000102218.6 | transcript | ENST00000218340.4 | protein_coding | 1/4 | chrX | 46851838 | |||||||
| chrX:46851983 | C | T | 3 | a0001c0001t0002g0150 a0001c0001t0002g0151 a0001c0001t0002g0152 |
3 | HG02109.hp2 HG02970.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.103-1493C>T | RP2 | ENSG00000102218.6 | transcript | ENST00000218340.4 | protein_coding | 1/4 | chrX | 46851983 | |||||||
| chrX:46852022 | G | A | 1 | a0001c0001t0001g0114 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.103-1454G>A | RP2 | ENSG00000102218.6 | transcript | ENST00000218340.4 | protein_coding | 1/4 | chrX | 46852022 | |||||||
| chrX:46852065 | G | A | 6 | a0001c0001t0001g0025 a0001c0001t0001g0043 a0001c0001t0001g0153 others(3): Show |
7 | HG01934.hp1 HG02258.hp1 HG02723.hp1 others(4): Show |
intron_variant | MODIFIER | c.103-1411G>A | RP2 | ENSG00000102218.6 | transcript | ENST00000218340.4 | protein_coding | 1/4 | chrX | 46852065 | |||||||
| chrX:46852263 | G | A | 3 | a0001c0001t0001g0084 a0001c0001t0001g0093 a0001c0001t0001g0213 |
3 | NA18952.hp1 NA19010.hp1 NA19086.hp1 |
intron_variant | MODIFIER | c.103-1213G>A | RP2 | ENSG00000102218.6 | transcript | ENST00000218340.4 | protein_coding | 1/4 | chrX | 46852263 | |||||||
| chrX:46852275 | G | A | 2 | a0001c0001t0001g0115 a0001c0001t0001g0116 |
2 | HG04204.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.103-1201G>A | RP2 | ENSG00000102218.6 | transcript | ENST00000218340.4 | protein_coding | 1/4 | chrX | 46852275 | |||||||
| chrX:46854609 | T | TA | 12 | a0001c0001t0001g0014 a0001c0001t0001g0047 a0001c0001t0001g0048 others(9): Show |
13 | HG01081.hp2 HG01243.hp1 HG01891.hp2 others(10): Show |
intron_variant | MODIFIER | c.768+469dupA | RP2 | ENSG00000102218.6 | transcript | ENST00000218340.4 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chrX | 46854609 | ||||||
| chrX:46854790 | G | T | 2 | a0001c0001t0001g0034 a0001c0001t0001g0035 |
2 | HG02735.hp1 HG03669.hp1 |
intron_variant | MODIFIER | c.768+649G>T | RP2 | ENSG00000102218.6 | transcript | ENST00000218340.4 | protein_coding | 2/4 | chrX | 46854790 | |||||||
| chrX:46855153 | C | T | 5 | a0001c0001t0001g0032 a0001c0001t0001g0086 a0001c0001t0001g0092 others(2): Show |
5 | HG00099.hp1 HG01106.hp1 HG01192.hp1 others(2): Show |
intron_variant | MODIFIER | c.768+1012C>T | RP2 | ENSG00000102218.6 | transcript | ENST00000218340.4 | protein_coding | 2/4 | chrX | 46855153 | |||||||
| chrX:46855228 | T | A | 1 | a0001c0001t0001g0049 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.768+1087T>A | RP2 | ENSG00000102218.6 | transcript | ENST00000218340.4 | protein_coding | 2/4 | chrX | 46855228 | |||||||
| chrX:46855259 | T | C | 1 | a0001c0001t0001g0105 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.768+1118T>C | RP2 | ENSG00000102218.6 | transcript | ENST00000218340.4 | protein_coding | 2/4 | chrX | 46855259 | |||||||
| chrX:46855445 | G | A | 1 | a0001c0001t0001g0115 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.768+1304G>A | RP2 | ENSG00000102218.6 | transcript | ENST00000218340.4 | protein_coding | 2/4 | chrX | 46855445 | |||||||
| chrX:46855797 | A | AT | 102 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0010 others(99): Show |
124 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(121): Show |
intron_variant | MODIFIER | c.768+1668dupT | RP2 | ENSG00000102218.6 | transcript | ENST00000218340.4 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chrX | 46855797 | ||||||
| chrX:46856155 | G | A | 133 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0010 others(130): Show |
159 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(156): Show |
intron_variant | MODIFIER | c.768+2014G>A | RP2 | ENSG00000102218.6 | transcript | ENST00000218340.4 | protein_coding | 2/4 | chrX | 46856155 | |||||||
| chrX:46856196 | A | C | 2 | a0001c0001t0001g0034 a0001c0001t0001g0035 |
2 | HG02735.hp1 HG03669.hp1 |
intron_variant | MODIFIER | c.768+2055A>C | RP2 | ENSG00000102218.6 | transcript | ENST00000218340.4 | protein_coding | 2/4 | chrX | 46856196 | |||||||
| chrX:46856702 | C | A | 2 | a0001c0001t0001g0034 a0001c0001t0001g0035 |
2 | HG02735.hp1 HG03669.hp1 |
intron_variant | MODIFIER | c.768+2561C>A | RP2 | ENSG00000102218.6 | transcript | ENST00000218340.4 | protein_coding | 2/4 | chrX | 46856702 | |||||||
| chrX:46857138 | A | AT | 22 | a0001c0001t0001g0014 a0001c0001t0001g0034 a0001c0001t0001g0035 others(19): Show |
23 | HG01081.hp2 HG01243.hp1 HG01891.hp1 others(20): Show |
intron_variant | MODIFIER | c.769-2838dupT | RP2 | ENSG00000102218.6 | transcript | ENST00000218340.4 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chrX | 46857138 | ||||||
| chrX:46857328 | G | A | 3 | a0001c0001t0002g0081 a0001c0001t0002g0082 a0001c0001t0002g0083 |
3 | HG02622.hp1 HG03453.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.769-2660G>A | RP2 | ENSG00000102218.6 | transcript | ENST00000218340.4 | protein_coding | 2/4 | chrX | 46857328 | |||||||
| chrX:46857597 | G | A | 2 | a0001c0001t0002g0006 a0001c0001t0002g0069 |
5 | NA18945.hp1 NA18957.hp2 NA19011.hp2 others(2): Show |
intron_variant | MODIFIER | c.769-2391G>A | RP2 | ENSG00000102218.6 | transcript | ENST00000218340.4 | protein_coding | 2/4 | chrX | 46857597 | |||||||
| chrX:46858474 | A | AT | 8 | a0001c0001t0001g0014 a0001c0001t0001g0047 a0001c0001t0001g0048 others(5): Show |
9 | HG01081.hp2 HG01243.hp1 HG01891.hp2 others(6): Show |
intron_variant | MODIFIER | c.769-1501dupT | RP2 | ENSG00000102218.6 | transcript | ENST00000218340.4 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chrX | 46858474 | ||||||
| chrX:46858667 | C | A | 12 | a0001c0001t0002g0006 a0001c0001t0002g0069 a0001c0001t0002g0072 others(9): Show |
15 | HG02109.hp2 HG02257.hp1 HG02622.hp1 others(12): Show |
intron_variant | MODIFIER | c.769-1321C>A | RP2 | ENSG00000102218.6 | transcript | ENST00000218340.4 | protein_coding | 2/4 | chrX | 46858667 | |||||||
| chrX:46858736 | G | A | 1 | a0001c0001t0001g0176 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.769-1252G>A | RP2 | ENSG00000102218.6 | transcript | ENST00000218340.4 | protein_coding | 2/4 | chrX | 46858736 | |||||||
| chrX:46859217 | T | G | 1 | a0001c0001t0001g0088 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.769-771T>G | RP2 | ENSG00000102218.6 | transcript | ENST00000218340.4 | protein_coding | 2/4 | chrX | 46859217 | |||||||
| chrX:46859327 | T | A | 2 | a0001c0001t0001g0034 a0001c0001t0001g0035 |
2 | HG02735.hp1 HG03669.hp1 |
intron_variant | MODIFIER | c.769-661T>A | RP2 | ENSG00000102218.6 | transcript | ENST00000218340.4 | protein_coding | 2/4 | chrX | 46859327 | |||||||
| chrX:46859488 | C | CA | 8 | a0001c0001t0001g0027 a0001c0001t0001g0065 a0001c0001t0001g0070 others(5): Show |
9 | HG01255.hp1 HG02055.hp1 HG02717.hp1 others(6): Show |
intron_variant | MODIFIER | c.769-485dupA | RP2 | ENSG00000102218.6 | transcript | ENST00000218340.4 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chrX | 46859488 | ||||||
| chrX:46859488 | CA | C | 11 | a0001c0001t0001g0034 a0001c0001t0001g0035 a0001c0001t0001g0038 others(8): Show |
11 | HG01891.hp1 HG01928.hp1 HG02451.hp2 others(8): Show |
intron_variant | MODIFIER | c.769-485delA | RP2 | ENSG00000102218.6 | transcript | ENST00000218340.4 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chrX | 46859488 | ||||||
| chrX:46859569 | T | C | 1 | a0001c0001t0001g0084 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.769-419T>C | RP2 | ENSG00000102218.6 | transcript | ENST00000218340.4 | protein_coding | 2/4 | chrX | 46859569 | |||||||
| chrX:46859776 | A | G | 2 | a0001c0001t0001g0034 a0001c0001t0001g0035 |
2 | HG02735.hp1 HG03669.hp1 |
intron_variant | MODIFIER | c.769-212A>G | RP2 | ENSG00000102218.6 | transcript | ENST00000218340.4 | protein_coding | 2/4 | chrX | 46859776 | |||||||
| chrX:46860267 | G | A | 1 | a0001c0001t0001g0205 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.883+165G>A | RP2 | ENSG00000102218.6 | transcript | ENST00000218340.4 | protein_coding | 3/4 | chrX | 46860267 | |||||||
| chrX:46860277 | C | T | 2 | a0001c0001t0001g0034 a0001c0001t0001g0035 |
2 | HG02735.hp1 HG03669.hp1 |
intron_variant | MODIFIER | c.883+175C>T | RP2 | ENSG00000102218.6 | transcript | ENST00000218340.4 | protein_coding | 3/4 | chrX | 46860277 | |||||||
| chrX:46860391 | C | A | 2 | a0001c0001t0001g0094 a0001c0001t0001g0095 |
2 | HG01358.hp1 HG04115.hp1 |
intron_variant | MODIFIER | c.883+289C>A | RP2 | ENSG00000102218.6 | transcript | ENST00000218340.4 | protein_coding | 3/4 | chrX | 46860391 | |||||||
| chrX:46860478 | T | G | 1 | a0001c0001t0001g0117 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.883+376T>G | RP2 | ENSG00000102218.6 | transcript | ENST00000218340.4 | protein_coding | 3/4 | chrX | 46860478 | |||||||
| chrX:46860637 | A | T | 1 | a0001c0001t0001g0102 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.883+535A>T | RP2 | ENSG00000102218.6 | transcript | ENST00000218340.4 | protein_coding | 3/4 | chrX | 46860637 | |||||||
| chrX:46860666 | T | G | 1 | a0001c0001t0001g0186 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.883+564T>G | RP2 | ENSG00000102218.6 | transcript | ENST00000218340.4 | protein_coding | 3/4 | chrX | 46860666 | |||||||
| chrX:46860960 | AAGTATTA others(4): Show |
A | 3 | a0001c0001t0002g0150 a0001c0001t0002g0151 a0001c0001t0002g0152 |
3 | HG02109.hp2 HG02970.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.883+865_883+875del others(11): Show |
RP2 | ENSG00000102218.6 | transcript | ENST00000218340.4 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chrX | 46860960 | ||||||
| chrX:46861221 | C | T | 1 | a0001c0001t0001g0089 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.883+1119C>T | RP2 | ENSG00000102218.6 | transcript | ENST00000218340.4 | protein_coding | 3/4 | chrX | 46861221 | |||||||
| chrX:46861229 | C | G | 1 | a0001c0001t0001g0155 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.883+1127C>G | RP2 | ENSG00000102218.6 | transcript | ENST00000218340.4 | protein_coding | 3/4 | chrX | 46861229 | |||||||
| chrX:46861271 | G | A | 1 | a0001c0001t0001g0187 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.883+1169G>A | RP2 | ENSG00000102218.6 | transcript | ENST00000218340.4 | protein_coding | 3/4 | chrX | 46861271 | |||||||
| chrX:46861367 | T | C | 1 | a0001c0001t0004g0139 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.883+1265T>C | RP2 | ENSG00000102218.6 | transcript | ENST00000218340.4 | protein_coding | 3/4 | chrX | 46861367 | |||||||
| chrX:46861768 | G | A | 1 | a0001c0001t0004g0139 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.883+1666G>A | RP2 | ENSG00000102218.6 | transcript | ENST00000218340.4 | protein_coding | 3/4 | chrX | 46861768 | |||||||
| chrX:46861772 | T | C | 1 | a0001c0001t0001g0096 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.883+1670T>C | RP2 | ENSG00000102218.6 | transcript | ENST00000218340.4 | protein_coding | 3/4 | chrX | 46861772 | |||||||
| chrX:46861797 | T | C | 4 | a0001c0001t0003g0013 a0001c0001t0003g0040 a0001c0001t0003g0041 others(1): Show |
5 | HG02622.hp2 HG02818.hp1 HG02970.hp1 others(2): Show |
intron_variant | MODIFIER | c.883+1695T>C | RP2 | ENSG00000102218.6 | transcript | ENST00000218340.4 | protein_coding | 3/4 | chrX | 46861797 | |||||||
| chrX:46861835 | T | G | 1 | a0001c0001t0001g0056 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.883+1733T>G | RP2 | ENSG00000102218.6 | transcript | ENST00000218340.4 | protein_coding | 3/4 | chrX | 46861835 | |||||||
| chrX:46862145 | G | A | 1 | a0001c0001t0001g0037 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.883+2043G>A | RP2 | ENSG00000102218.6 | transcript | ENST00000218340.4 | protein_coding | 3/4 | chrX | 46862145 | |||||||
| chrX:46862388 | T | C | 6 | a0001c0001t0001g0025 a0001c0001t0001g0043 a0001c0001t0001g0153 others(3): Show |
7 | HG01934.hp1 HG02258.hp1 HG02723.hp1 others(4): Show |
intron_variant | MODIFIER | c.883+2286T>C | RP2 | ENSG00000102218.6 | transcript | ENST00000218340.4 | protein_coding | 3/4 | chrX | 46862388 | |||||||
| chrX:46862412 | A | G | 1 | a0001c0001t0001g0202 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.883+2310A>G | RP2 | ENSG00000102218.6 | transcript | ENST00000218340.4 | protein_coding | 3/4 | chrX | 46862412 | |||||||
| chrX:46862427 | A | C | 1 | a0001c0001t0001g0038 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.883+2325A>C | RP2 | ENSG00000102218.6 | transcript | ENST00000218340.4 | protein_coding | 3/4 | chrX | 46862427 | |||||||
| chrX:46862427 | A | G | 2 | a0001c0001t0001g0021 a0001c0001t0001g0144 |
3 | NA18955.hp1 NA18977.hp1 NA19006.hp1 |
intron_variant | MODIFIER | c.883+2325A>G | RP2 | ENSG00000102218.6 | transcript | ENST00000218340.4 | protein_coding | 3/4 | chrX | 46862427 | |||||||
| chrX:46862435 | C | T | 1 | a0001c0001t0001g0202 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.883+2333C>T | RP2 | ENSG00000102218.6 | transcript | ENST00000218340.4 | protein_coding | 3/4 | chrX | 46862435 | |||||||
| chrX:46862436 | A | G | 2 | a0001c0001t0001g0134 a0001c0001t0001g0202 |
2 | HG01123.hp2 HG02129.hp1 |
intron_variant | MODIFIER | c.883+2334A>G | RP2 | ENSG00000102218.6 | transcript | ENST00000218340.4 | protein_coding | 3/4 | chrX | 46862436 | |||||||
| chrX:46862443 | A | G | 2 | a0001c0001t0001g0134 a0001c0001t0001g0202 |
2 | HG01123.hp2 HG02129.hp1 |
intron_variant | MODIFIER | c.883+2341A>G | RP2 | ENSG00000102218.6 | transcript | ENST00000218340.4 | protein_coding | 3/4 | chrX | 46862443 | |||||||
| chrX:46862457 | A | G | 1 | a0001c0001t0001g0134 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.883+2355A>G | RP2 | ENSG00000102218.6 | transcript | ENST00000218340.4 | protein_coding | 3/4 | chrX | 46862457 | |||||||
| chrX:46862471 | T | C | 1 | a0001c0001t0001g0158 | 1 | NA18992.hp1 | intron_variant | MODIFIER | c.883+2369T>C | RP2 | ENSG00000102218.6 | transcript | ENST00000218340.4 | protein_coding | 3/4 | chrX | 46862471 | |||||||
| chrX:46862510 | A | G | 77 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0010 others(74): Show |
95 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(92): Show |
intron_variant | MODIFIER | c.883+2408A>G | RP2 | ENSG00000102218.6 | transcript | ENST00000218340.4 | protein_coding | 3/4 | chrX | 46862510 | |||||||
| chrX:46862516 | C | T | 8 | a0001c0001t0001g0025 a0001c0001t0001g0038 a0001c0001t0001g0043 others(5): Show |
9 | HG01934.hp1 HG02258.hp1 HG02723.hp1 others(6): Show |
intron_variant | MODIFIER | c.883+2414C>T | RP2 | ENSG00000102218.6 | transcript | ENST00000218340.4 | protein_coding | 3/4 | chrX | 46862516 | |||||||
| chrX:46862553 | A | G | 1 | a0001c0001t0001g0158 | 1 | NA18992.hp1 | intron_variant | MODIFIER | c.883+2451A>G | RP2 | ENSG00000102218.6 | transcript | ENST00000218340.4 | protein_coding | 3/4 | chrX | 46862553 | |||||||
| chrX:46862576 | C | T | 2 | a0001c0001t0001g0129 a0001c0001t0001g0130 |
2 | HG00741.hp2 HG01070.hp1 |
intron_variant | MODIFIER | c.883+2474C>T | RP2 | ENSG00000102218.6 | transcript | ENST00000218340.4 | protein_coding | 3/4 | chrX | 46862576 | |||||||
| chrX:46862591 | T | C | 3 | a0001c0001t0001g0018 a0001c0001t0001g0073 a0001c0001t0001g0074 |
4 | HG02559.hp2 HG02886.hp1 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.883+2489T>C | RP2 | ENSG00000102218.6 | transcript | ENST00000218340.4 | protein_coding | 3/4 | chrX | 46862591 | |||||||
| chrX:46862593 | G | A | 2 | a0001c0001t0001g0129 a0001c0001t0001g0130 |
2 | HG00741.hp2 HG01070.hp1 |
intron_variant | MODIFIER | c.883+2491G>A | RP2 | ENSG00000102218.6 | transcript | ENST00000218340.4 | protein_coding | 3/4 | chrX | 46862593 | |||||||
| chrX:46862616 | C | T | 3 | a0001c0001t0003g0013 a0001c0001t0003g0041 a0001c0001t0003g0042 |
4 | HG02622.hp2 HG02818.hp1 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.883+2514C>T | RP2 | ENSG00000102218.6 | transcript | ENST00000218340.4 | protein_coding | 3/4 | chrX | 46862616 | |||||||
| chrX:46862683 | C | A | 2 | a0001c0001t0001g0164 a0001c0001t0001g0182 |
2 | HG00280.hp1 NA20905.hp1 |
intron_variant | MODIFIER | c.883+2581C>A | RP2 | ENSG00000102218.6 | transcript | ENST00000218340.4 | protein_coding | 3/4 | chrX | 46862683 | |||||||
| chrX:46862905 | G | C | 2 | a0001c0001t0001g0034 a0001c0001t0001g0035 |
2 | HG02735.hp1 HG03669.hp1 |
intron_variant | MODIFIER | c.883+2803G>C | RP2 | ENSG00000102218.6 | transcript | ENST00000218340.4 | protein_coding | 3/4 | chrX | 46862905 | |||||||
| chrX:46863031 | A | C | 1 | a0001c0001t0004g0139 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.883+2929A>C | RP2 | ENSG00000102218.6 | transcript | ENST00000218340.4 | protein_coding | 3/4 | chrX | 46863031 | |||||||
| chrX:46863046 | A | T | 1 | a0001c0001t0004g0139 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.883+2944A>T | RP2 | ENSG00000102218.6 | transcript | ENST00000218340.4 | protein_coding | 3/4 | chrX | 46863046 | |||||||
| chrX:46863083 | T | C | 3 | a0001c0001t0001g0153 a0001c0001t0001g0154 a0001c0001t0001g0155 |
3 | HG02809.hp2 NA19030.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.883+2981T>C | RP2 | ENSG00000102218.6 | transcript | ENST00000218340.4 | protein_coding | 3/4 | chrX | 46863083 | |||||||
| chrX:46863291 | A | G | 1 | a0001c0001t0001g0095 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.883+3189A>G | RP2 | ENSG00000102218.6 | transcript | ENST00000218340.4 | protein_coding | 3/4 | chrX | 46863291 | |||||||
| chrX:46863358 | G | T | 1 | a0001c0001t0005g0174 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.883+3256G>T | RP2 | ENSG00000102218.6 | transcript | ENST00000218340.4 | protein_coding | 3/4 | chrX | 46863358 | |||||||
| chrX:46863411 | T | C | 1 | a0001c0001t0004g0039 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.883+3309T>C | RP2 | ENSG00000102218.6 | transcript | ENST00000218340.4 | protein_coding | 3/4 | chrX | 46863411 | |||||||
| chrX:46863460 | C | T | 1 | a0001c0001t0001g0159 | 1 | NA19089.hp1 | intron_variant | MODIFIER | c.883+3358C>T | RP2 | ENSG00000102218.6 | transcript | ENST00000218340.4 | protein_coding | 3/4 | chrX | 46863460 | |||||||
| chrX:46863832 | T | A | 2 | a0001c0001t0002g0006 a0001c0001t0002g0069 |
5 | NA18945.hp1 NA18957.hp2 NA19011.hp2 others(2): Show |
intron_variant | MODIFIER | c.883+3730T>A | RP2 | ENSG00000102218.6 | transcript | ENST00000218340.4 | protein_coding | 3/4 | chrX | 46863832 | |||||||
| chrX:46863950 | C | A | 2 | a0001c0001t0001g0147 a0001c0001t0001g0149 |
2 | NA19001.hp2 NA19084.hp1 |
intron_variant | MODIFIER | c.883+3848C>A | RP2 | ENSG00000102218.6 | transcript | ENST00000218340.4 | protein_coding | 3/4 | chrX | 46863950 | |||||||
| chrX:46864047 | C | A | 1 | a0002c0002t0001g0118 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.883+3945C>A | RP2 | ENSG00000102218.6 | transcript | ENST00000218340.4 | protein_coding | 3/4 | chrX | 46864047 | |||||||
| chrX:46864290 | G | A | 1 | a0001c0001t0001g0106 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.883+4188G>A | RP2 | ENSG00000102218.6 | transcript | ENST00000218340.4 | protein_coding | 3/4 | chrX | 46864290 | |||||||
| chrX:46864347 | C | CT | 24 | a0001c0001t0001g0014 a0001c0001t0001g0019 a0001c0001t0001g0023 others(21): Show |
28 | HG01081.hp2 HG01109.hp1 HG01891.hp2 others(25): Show |
intron_variant | MODIFIER | c.883+4262dupT | RP2 | ENSG00000102218.6 | transcript | ENST00000218340.4 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chrX | 46864347 | ||||||
| chrX:46864347 | C | CTT | 6 | a0001c0001t0001g0049 a0001c0001t0001g0050 a0001c0001t0001g0051 others(3): Show |
6 | HG01243.hp1 HG02145.hp1 HG02280.hp1 others(3): Show |
intron_variant | MODIFIER | c.883+4261_883+4262d others(4): Show |
RP2 | ENSG00000102218.6 | transcript | ENST00000218340.4 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chrX | 46864347 | ||||||
| chrX:46864347 | CT | C | 6 | a0001c0001t0001g0037 a0001c0001t0001g0062 a0001c0001t0001g0107 others(3): Show |
6 | HG02486.hp1 HG02615.hp2 HG02647.hp1 others(3): Show |
intron_variant | MODIFIER | c.883+4262delT | RP2 | ENSG00000102218.6 | transcript | ENST00000218340.4 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chrX | 46864347 | ||||||
| chrX:46864411 | A | G | 8 | a0001c0001t0001g0014 a0001c0001t0001g0047 a0001c0001t0001g0048 others(5): Show |
9 | HG01081.hp2 HG01243.hp1 HG01891.hp2 others(6): Show |
intron_variant | MODIFIER | c.883+4309A>G | RP2 | ENSG00000102218.6 | transcript | ENST00000218340.4 | protein_coding | 3/4 | chrX | 46864411 | |||||||
| chrX:46864657 | C | T | 3 | a0001c0001t0002g0150 a0001c0001t0002g0151 a0001c0001t0002g0152 |
3 | HG02109.hp2 HG02970.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.883+4555C>T | RP2 | ENSG00000102218.6 | transcript | ENST00000218340.4 | protein_coding | 3/4 | chrX | 46864657 | |||||||
| chrX:46864674 | G | T | 92 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0010 others(89): Show |
110 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(107): Show |
intron_variant | MODIFIER | c.883+4572G>T | RP2 | ENSG00000102218.6 | transcript | ENST00000218340.4 | protein_coding | 3/4 | chrX | 46864674 | |||||||
| chrX:46865229 | A | G | 1 | a0001c0001t0001g0020 | 2 | HG01099.hp1 NA20805.hp1 |
intron_variant | MODIFIER | c.883+5127A>G | RP2 | ENSG00000102218.6 | transcript | ENST00000218340.4 | protein_coding | 3/4 | chrX | 46865229 | |||||||
| chrX:46865478 | G | C | 1 | a0001c0001t0003g0046 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.883+5376G>C | RP2 | ENSG00000102218.6 | transcript | ENST00000218340.4 | protein_coding | 3/4 | chrX | 46865478 | |||||||
| chrX:46865704 | C | T | 13 | a0001c0001t0001g0014 a0001c0001t0001g0047 a0001c0001t0001g0048 others(10): Show |
14 | HG01081.hp2 HG01243.hp1 HG01891.hp2 others(11): Show |
intron_variant | MODIFIER | c.883+5602C>T | RP2 | ENSG00000102218.6 | transcript | ENST00000218340.4 | protein_coding | 3/4 | chrX | 46865704 | |||||||
| chrX:46866017 | A | G | 1 | a0001c0003t0001g0044 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.883+5915A>G | RP2 | ENSG00000102218.6 | transcript | ENST00000218340.4 | protein_coding | 3/4 | chrX | 46866017 | |||||||
| chrX:46866203 | G | A | 2 | a0001c0001t0001g0030 a0004c0004t0001g0030 |
2 | NA18971.hp1 NA19007.hp1 |
intron_variant | MODIFIER | c.883+6101G>A | RP2 | ENSG00000102218.6 | transcript | ENST00000218340.4 | protein_coding | 3/4 | chrX | 46866203 | |||||||
| chrX:46866366 | G | GTATC | 13 | a0001c0001t0001g0121 a0001c0001t0002g0072 a0001c0001t0002g0079 others(10): Show |
14 | HG02109.hp2 HG02257.hp1 HG02622.hp1 others(11): Show |
intron_variant | MODIFIER | c.883+6280_883+6283d others(6): Show |
RP2 | ENSG00000102218.6 | transcript | ENST00000218340.4 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chrX | 46866366 | ||||||
| chrX:46866367 | T | C | 3 | a0001c0001t0001g0037 a0001c0001t0001g0038 a0001c0001t0004g0039 |
3 | HG02486.hp1 HG02647.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.883+6265T>C | RP2 | ENSG00000102218.6 | transcript | ENST00000218340.4 | protein_coding | 3/4 | chrX | 46866367 | |||||||
| chrX:46866534 | A | G | 4 | a0001c0001t0001g0029 a0001c0001t0001g0162 a0001c0001t0001g0163 others(1): Show |
5 | HG01167.hp1 HG01169.hp1 HG01884.hp2 others(2): Show |
intron_variant | MODIFIER | c.883+6432A>G | RP2 | ENSG00000102218.6 | transcript | ENST00000218340.4 | protein_coding | 3/4 | chrX | 46866534 | |||||||
| chrX:46867131 | C | T | 1 | a0001c0001t0001g0065 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.883+7029C>T | RP2 | ENSG00000102218.6 | transcript | ENST00000218340.4 | protein_coding | 3/4 | chrX | 46867131 | |||||||
| chrX:46867321 | G | A | 1 | a0001c0001t0001g0156 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.883+7219G>A | RP2 | ENSG00000102218.6 | transcript | ENST00000218340.4 | protein_coding | 3/4 | chrX | 46867321 | |||||||
| chrX:46867828 | G | A | 1 | a0001c0001t0001g0068 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.883+7726G>A | RP2 | ENSG00000102218.6 | transcript | ENST00000218340.4 | protein_coding | 3/4 | chrX | 46867828 | |||||||
| chrX:46868051 | T | C | 1 | a0001c0001t0001g0096 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.883+7949T>C | RP2 | ENSG00000102218.6 | transcript | ENST00000218340.4 | protein_coding | 3/4 | chrX | 46868051 | |||||||
| chrX:46868309 | G | A | 4 | a0001c0001t0001g0049 a0001c0001t0001g0050 a0001c0001t0001g0051 others(1): Show |
4 | HG02145.hp1 HG02280.hp1 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.883+8207G>A | RP2 | ENSG00000102218.6 | transcript | ENST00000218340.4 | protein_coding | 3/4 | chrX | 46868309 | |||||||
| chrX:46868583 | G | A | 18 | a0001c0001t0001g0007 a0001c0001t0001g0009 a0001c0001t0001g0021 others(15): Show |
24 | HG00558.hp2 HG00621.hp1 HG02132.hp1 others(21): Show |
intron_variant | MODIFIER | c.883+8481G>A | RP2 | ENSG00000102218.6 | transcript | ENST00000218340.4 | protein_coding | 3/4 | chrX | 46868583 | |||||||
| chrX:46868785 | C | CA | 9 | a0001c0001t0001g0043 a0001c0001t0001g0049 a0001c0001t0001g0070 others(6): Show |
9 | HG02055.hp1 HG02071.hp1 HG02258.hp1 others(6): Show |
intron_variant | MODIFIER | c.883+8701dupA | RP2 | ENSG00000102218.6 | transcript | ENST00000218340.4 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chrX | 46868785 | ||||||
| chrX:46868838 | G | A | 2 | a0001c0001t0001g0034 a0001c0001t0001g0035 |
2 | HG02735.hp1 HG03669.hp1 |
intron_variant | MODIFIER | c.884-8667G>A | RP2 | ENSG00000102218.6 | transcript | ENST00000218340.4 | protein_coding | 3/4 | chrX | 46868838 | |||||||
| chrX:46869075 | G | T | 2 | a0001c0001t0001g0034 a0001c0001t0001g0035 |
2 | HG02735.hp1 HG03669.hp1 |
intron_variant | MODIFIER | c.884-8430G>T | RP2 | ENSG00000102218.6 | transcript | ENST00000218340.4 | protein_coding | 3/4 | chrX | 46869075 | |||||||
| chrX:46869300 | CT | C | 133 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0010 others(130): Show |
159 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(156): Show |
intron_variant | MODIFIER | c.884-8190delT | RP2 | ENSG00000102218.6 | transcript | ENST00000218340.4 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chrX | 46869300 | ||||||
| chrX:46869578 | G | A | 3 | a0001c0001t0001g0018 a0001c0001t0001g0073 a0001c0001t0001g0074 |
4 | HG02559.hp2 HG02886.hp1 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.884-7927G>A | RP2 | ENSG00000102218.6 | transcript | ENST00000218340.4 | protein_coding | 3/4 | chrX | 46869578 | |||||||
| chrX:46869591 | A | T | 1 | a0001c0001t0005g0172 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.884-7914A>T | RP2 | ENSG00000102218.6 | transcript | ENST00000218340.4 | protein_coding | 3/4 | chrX | 46869591 | |||||||
| chrX:46869606 | C | CT | 13 | a0001c0001t0001g0019 a0001c0001t0001g0052 a0001c0001t0001g0122 others(10): Show |
14 | HG01192.hp1 HG01981.hp1 HG01981.hp2 others(11): Show |
intron_variant | MODIFIER | c.884-7879dupT | RP2 | ENSG00000102218.6 | transcript | ENST00000218340.4 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chrX | 46869606 | ||||||
| chrX:46869703 | G | A | 2 | a0001c0001t0001g0034 a0001c0001t0001g0035 |
2 | HG02735.hp1 HG03669.hp1 |
intron_variant | MODIFIER | c.884-7802G>A | RP2 | ENSG00000102218.6 | transcript | ENST00000218340.4 | protein_coding | 3/4 | chrX | 46869703 | |||||||
| chrX:46869704 | G | C | 1 | a0001c0001t0001g0121 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.884-7801G>C | RP2 | ENSG00000102218.6 | transcript | ENST00000218340.4 | protein_coding | 3/4 | chrX | 46869704 | |||||||
| chrX:46869743 | G | A | 1 | a0001c0001t0001g0073 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.884-7762G>A | RP2 | ENSG00000102218.6 | transcript | ENST00000218340.4 | protein_coding | 3/4 | chrX | 46869743 | |||||||
| chrX:46870140 | C | T | 1 | a0001c0001t0001g0134 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.884-7365C>T | RP2 | ENSG00000102218.6 | transcript | ENST00000218340.4 | protein_coding | 3/4 | chrX | 46870140 | |||||||
| chrX:46870253 | T | G | 2 | a0001c0001t0001g0034 a0001c0001t0001g0035 |
2 | HG02735.hp1 HG03669.hp1 |
intron_variant | MODIFIER | c.884-7252T>G | RP2 | ENSG00000102218.6 | transcript | ENST00000218340.4 | protein_coding | 3/4 | chrX | 46870253 | |||||||
| chrX:46870674 | A | G | 2 | a0001c0001t0001g0034 a0001c0001t0001g0035 |
2 | HG02735.hp1 HG03669.hp1 |
intron_variant | MODIFIER | c.884-6831A>G | RP2 | ENSG00000102218.6 | transcript | ENST00000218340.4 | protein_coding | 3/4 | chrX | 46870674 | |||||||
| chrX:46870789 | G | T | 2 | a0001c0001t0002g0006 a0001c0001t0002g0069 |
5 | NA18945.hp1 NA18957.hp2 NA19011.hp2 others(2): Show |
intron_variant | MODIFIER | c.884-6716G>T | RP2 | ENSG00000102218.6 | transcript | ENST00000218340.4 | protein_coding | 3/4 | chrX | 46870789 | |||||||
| chrX:46870868 | T | C | 3 | a0001c0001t0001g0037 a0001c0001t0001g0038 a0001c0001t0004g0039 |
3 | HG02486.hp1 HG02647.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.884-6637T>C | RP2 | ENSG00000102218.6 | transcript | ENST00000218340.4 | protein_coding | 3/4 | chrX | 46870868 | |||||||
| chrX:46871009 | C | T | 1 | a0001c0001t0001g0115 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.884-6496C>T | RP2 | ENSG00000102218.6 | transcript | ENST00000218340.4 | protein_coding | 3/4 | chrX | 46871009 | |||||||
| chrX:46871021 | C | CT | 43 | a0001c0001t0001g0014 a0001c0001t0001g0023 a0001c0001t0001g0043 others(40): Show |
46 | HG00438.hp1 HG00558.hp1 HG01081.hp2 others(43): Show |
intron_variant | MODIFIER | c.884-6458dupT | RP2 | ENSG00000102218.6 | transcript | ENST00000218340.4 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chrX | 46871021 | ||||||
| chrX:46871021 | CT | C | 8 | a0001c0001t0001g0034 a0001c0001t0001g0076 a0001c0001t0001g0088 others(5): Show |
8 | HG00140.hp1 HG02280.hp2 HG02451.hp1 others(5): Show |
intron_variant | MODIFIER | c.884-6458delT | RP2 | ENSG00000102218.6 | transcript | ENST00000218340.4 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chrX | 46871021 | ||||||
| chrX:46871115 | G | A | 1 | a0001c0001t0001g0121 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.884-6390G>A | RP2 | ENSG00000102218.6 | transcript | ENST00000218340.4 | protein_coding | 3/4 | chrX | 46871115 | |||||||
| chrX:46871146 | C | T | 1 | a0001c0001t0001g0138 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.884-6359C>T | RP2 | ENSG00000102218.6 | transcript | ENST00000218340.4 | protein_coding | 3/4 | chrX | 46871146 | |||||||
| chrX:46871268 | C | T | 2 | a0001c0001t0001g0034 a0001c0001t0001g0035 |
2 | HG02735.hp1 HG03669.hp1 |
intron_variant | MODIFIER | c.884-6237C>T | RP2 | ENSG00000102218.6 | transcript | ENST00000218340.4 | protein_coding | 3/4 | chrX | 46871268 | |||||||
| chrX:46871513 | G | A | 1 | a0001c0001t0001g0050 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.884-5992G>A | RP2 | ENSG00000102218.6 | transcript | ENST00000218340.4 | protein_coding | 3/4 | chrX | 46871513 | |||||||
| chrX:46871797 | G | C | 1 | a0001c0001t0001g0162 | 1 | HG02897.hp2 | intron_variant | MODIFIER | c.884-5708G>C | RP2 | ENSG00000102218.6 | transcript | ENST00000218340.4 | protein_coding | 3/4 | chrX | 46871797 | |||||||
| chrX:46872014 | C | T | 6 | a0001c0001t0001g0029 a0001c0001t0001g0162 a0001c0001t0001g0163 others(3): Show |
7 | HG01167.hp1 HG01169.hp1 HG01884.hp2 others(4): Show |
intron_variant | MODIFIER | c.884-5491C>T | RP2 | ENSG00000102218.6 | transcript | ENST00000218340.4 | protein_coding | 3/4 | chrX | 46872014 | |||||||
| chrX:46872240 | T | C | 1 | a0001c0001t0001g0206 | 1 | HG01258.hp1 | intron_variant | MODIFIER | c.884-5265T>C | RP2 | ENSG00000102218.6 | transcript | ENST00000218340.4 | protein_coding | 3/4 | chrX | 46872240 | |||||||
| chrX:46872476 | A | G | 1 | a0001c0001t0001g0024 | 2 | NA18984.hp1 NA19065.hp1 |
intron_variant | MODIFIER | c.884-5029A>G | RP2 | ENSG00000102218.6 | transcript | ENST00000218340.4 | protein_coding | 3/4 | chrX | 46872476 | |||||||
| chrX:46872773 | T | G | 4 | a0001c0001t0001g0166 a0001c0001t0001g0167 a0001c0001t0001g0181 others(1): Show |
4 | HG00438.hp1 NA18973.hp2 NA19010.hp2 others(1): Show |
intron_variant | MODIFIER | c.884-4732T>G | RP2 | ENSG00000102218.6 | transcript | ENST00000218340.4 | protein_coding | 3/4 | chrX | 46872773 | |||||||
| chrX:46872862 | C | T | 1 | a0002c0002t0001g0125 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.884-4643C>T | RP2 | ENSG00000102218.6 | transcript | ENST00000218340.4 | protein_coding | 3/4 | chrX | 46872862 | |||||||
| chrX:46873114 | G | T | 1 | a0001c0001t0001g0121 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.884-4391G>T | RP2 | ENSG00000102218.6 | transcript | ENST00000218340.4 | protein_coding | 3/4 | chrX | 46873114 | |||||||
| chrX:46873279 | T | A | 1 | a0001c0001t0001g0134 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.884-4226T>A | RP2 | ENSG00000102218.6 | transcript | ENST00000218340.4 | protein_coding | 3/4 | chrX | 46873279 | |||||||
| chrX:46873541 | A | G | 1 | a0001c0001t0001g0124 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.884-3964A>G | RP2 | ENSG00000102218.6 | transcript | ENST00000218340.4 | protein_coding | 3/4 | chrX | 46873541 | |||||||
| chrX:46874825 | G | T | 1 | a0001c0001t0001g0191 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.884-2680G>T | RP2 | ENSG00000102218.6 | transcript | ENST00000218340.4 | protein_coding | 3/4 | chrX | 46874825 | |||||||
| chrX:46874912 | G | A | 1 | a0001c0001t0001g0189 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.884-2593G>A | RP2 | ENSG00000102218.6 | transcript | ENST00000218340.4 | protein_coding | 3/4 | chrX | 46874912 | |||||||
| chrX:46875295 | C | CT | 17 | a0001c0001t0001g0014 a0001c0001t0001g0023 a0001c0001t0001g0047 others(14): Show |
19 | HG01081.hp2 HG01243.hp1 HG01891.hp2 others(16): Show |
intron_variant | MODIFIER | c.884-2195dupT | RP2 | ENSG00000102218.6 | transcript | ENST00000218340.4 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chrX | 46875295 | ||||||
| chrX:46875295 | CT | C | 5 | a0001c0001t0001g0034 a0001c0001t0001g0035 a0001c0001t0001g0063 others(2): Show |
5 | HG02735.hp1 HG02895.hp1 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.884-2195delT | RP2 | ENSG00000102218.6 | transcript | ENST00000218340.4 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chrX | 46875295 | ||||||
| chrX:46875387 | G | A | 1 | a0001c0001t0009g0058 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.884-2118G>A | RP2 | ENSG00000102218.6 | transcript | ENST00000218340.4 | protein_coding | 3/4 | chrX | 46875387 | |||||||
| chrX:46875640 | G | A | 1 | a0001c0001t0001g0116 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.884-1865G>A | RP2 | ENSG00000102218.6 | transcript | ENST00000218340.4 | protein_coding | 3/4 | chrX | 46875640 | |||||||
| chrX:46875693 | T | TCTCCTTT others(17): Show |
1 | a0001c0001t0001g0200 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.884-1810_884-1787d others(26): Show |
RP2 | ENSG00000102218.6 | transcript | ENST00000218340.4 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chrX | 46875693 | ||||||
| chrX:46875969 | T | C | 202 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(199): Show |
255 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(252): Show |
intron_variant | MODIFIER | c.884-1536T>C | RP2 | ENSG00000102218.6 | transcript | ENST00000218340.4 | protein_coding | 3/4 | chrX | 46875969 | |||||||
| chrX:46876016 | A | T | 93 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0010 others(90): Show |
112 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(109): Show |
intron_variant | MODIFIER | c.884-1489A>T | RP2 | ENSG00000102218.6 | transcript | ENST00000218340.4 | protein_coding | 3/4 | chrX | 46876016 | |||||||
| chrX:46876055 | C | G | 2 | a0001c0001t0001g0034 a0001c0001t0001g0035 |
2 | HG02735.hp1 HG03669.hp1 |
intron_variant | MODIFIER | c.884-1450C>G | RP2 | ENSG00000102218.6 | transcript | ENST00000218340.4 | protein_coding | 3/4 | chrX | 46876055 | |||||||
| chrX:46876127 | AT | A | 93 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0010 others(90): Show |
112 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(109): Show |
intron_variant | MODIFIER | c.884-1368delT | RP2 | ENSG00000102218.6 | transcript | ENST00000218340.4 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chrX | 46876127 | ||||||
| chrX:46876162 | C | T | 1 | a0001c0001t0004g0211 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.884-1343C>T | RP2 | ENSG00000102218.6 | transcript | ENST00000218340.4 | protein_coding | 3/4 | chrX | 46876162 | |||||||
| chrX:46876418 | G | A | 12 | a0001c0001t0001g0014 a0001c0001t0001g0047 a0001c0001t0001g0048 others(9): Show |
13 | HG01081.hp2 HG01243.hp1 HG01891.hp2 others(10): Show |
intron_variant | MODIFIER | c.884-1087G>A | RP2 | ENSG00000102218.6 | transcript | ENST00000218340.4 | protein_coding | 3/4 | chrX | 46876418 | |||||||
| chrX:46876770 | G | A | 1 | a0001c0001t0003g0046 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.884-735G>A | RP2 | ENSG00000102218.6 | transcript | ENST00000218340.4 | protein_coding | 3/4 | chrX | 46876770 | |||||||
| chrX:46877020 | T | G | 5 | a0001c0001t0001g0075 a0001c0001t0001g0076 a0001c0001t0001g0077 others(2): Show |
5 | HG01891.hp1 HG02451.hp2 HG02615.hp1 others(2): Show |
intron_variant | MODIFIER | c.884-485T>G | RP2 | ENSG00000102218.6 | transcript | ENST00000218340.4 | protein_coding | 3/4 | chrX | 46877020 | |||||||
| chrX:46877283 | A | G | 1 | a0001c0001t0002g0072 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.884-222A>G | RP2 | ENSG00000102218.6 | transcript | ENST00000218340.4 | protein_coding | 3/4 | chrX | 46877283 | |||||||
| chrX:46877461 | A | G | 1 | a0001c0001t0001g0135 | 1 | HG03492.hp1 | intron_variant | MODIFIER | c.884-44A>G | RP2 | ENSG00000102218.6 | transcript | ENST00000218340.4 | protein_coding | 3/4 | chrX | 46877461 | |||||||
| chrX:46877650 | C | T | 1 | a0001c0001t0001g0120 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.969+60C>T | RP2 | ENSG00000102218.6 | transcript | ENST00000218340.4 | protein_coding | 4/4 | chrX | 46877650 | |||||||
| chrX:46877703 | G | GGT | 106 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0010 others(103): Show |
128 | HG00140.hp1 HG00280.hp1 HG00323.hp2 others(125): Show |
intron_variant | MODIFIER | c.969+142_969+143dup others(2): Show |
RP2 | ENSG00000102218.6 | transcript | ENST00000218340.4 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chrX | 46877703 | ||||||
| chrX:46877703 | G | GGTGT | 7 | a0001c0001t0001g0034 a0001c0001t0001g0036 a0001c0001t0001g0070 others(4): Show |
7 | HG00099.hp2 HG00544.hp1 HG02055.hp1 others(4): Show |
intron_variant | MODIFIER | c.969+140_969+143dup others(4): Show |
RP2 | ENSG00000102218.6 | transcript | ENST00000218340.4 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chrX | 46877703 | ||||||
| chrX:46877703 | G | GGTGTGT | 86 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(83): Show |
114 | HG00099.hp1 HG00323.hp1 HG00408.hp2 others(111): Show |
intron_variant | MODIFIER | c.969+138_969+143dup others(6): Show |
RP2 | ENSG00000102218.6 | transcript | ENST00000218340.4 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chrX | 46877703 | ||||||
| chrX:46877703 | G | GGTGTGTG others(1): Show |
3 | a0001c0001t0001g0004 a0001c0001t0001g0135 a0001c0001t0003g0046 |
6 | HG01069.hp1 HG01071.hp2 HG01993.hp2 others(3): Show |
intron_variant | MODIFIER | c.969+136_969+143dup others(8): Show |
RP2 | ENSG00000102218.6 | transcript | ENST00000218340.4 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chrX | 46877703 | ||||||
| chrX:46877703 | G | GGTGTGTG others(3): Show |
1 | a0001c0001t0001g0104 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.969+134_969+143dup others(10): Show |
RP2 | ENSG00000102218.6 | transcript | ENST00000218340.4 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chrX | 46877703 | ||||||
| chrX:46877703 | G | GGTGTGTG others(9): Show |
1 | a0001c0001t0001g0165 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.969+128_969+143dup others(16): Show |
RP2 | ENSG00000102218.6 | transcript | ENST00000218340.4 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chrX | 46877703 | ||||||
| chrX:46877734 | T | G | 1 | a0001c0001t0001g0168 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.969+144T>G | RP2 | ENSG00000102218.6 | transcript | ENST00000218340.4 | protein_coding | 4/4 | chrX | 46877734 | |||||||
| chrX:46878091 | T | C | 4 | a0001c0001t0003g0013 a0001c0001t0003g0040 a0001c0001t0003g0041 others(1): Show |
5 | HG02622.hp2 HG02818.hp1 HG02970.hp1 others(2): Show |
intron_variant | MODIFIER | c.969+501T>C | RP2 | ENSG00000102218.6 | transcript | ENST00000218340.4 | protein_coding | 4/4 | chrX | 46878091 | |||||||
| chrX:46878150 | G | A | 1 | a0001c0001t0001g0160 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.969+560G>A | RP2 | ENSG00000102218.6 | transcript | ENST00000218340.4 | protein_coding | 4/4 | chrX | 46878150 | |||||||
| chrX:46878237 | C | T | 1 | a0001c0001t0001g0067 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.969+647C>T | RP2 | ENSG00000102218.6 | transcript | ENST00000218340.4 | protein_coding | 4/4 | chrX | 46878237 | |||||||
| chrX:46878240 | A | G | 1 | a0001c0001t0001g0086 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.969+650A>G | RP2 | ENSG00000102218.6 | transcript | ENST00000218340.4 | protein_coding | 4/4 | chrX | 46878240 | |||||||
| chrX:46878245 | C | T | 1 | a0001c0001t0001g0059 | 1 | NA19001.hp1 | intron_variant | MODIFIER | c.969+655C>T | RP2 | ENSG00000102218.6 | transcript | ENST00000218340.4 | protein_coding | 4/4 | chrX | 46878245 | |||||||
| chrX:46878309 | G | A | 1 | a0001c0001t0001g0117 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.969+719G>A | RP2 | ENSG00000102218.6 | transcript | ENST00000218340.4 | protein_coding | 4/4 | chrX | 46878309 | |||||||
| chrX:46878371 | T | C | 12 | a0001c0001t0001g0014 a0001c0001t0001g0047 a0001c0001t0001g0048 others(9): Show |
13 | HG01081.hp2 HG01243.hp1 HG01891.hp2 others(10): Show |
intron_variant | MODIFIER | c.969+781T>C | RP2 | ENSG00000102218.6 | transcript | ENST00000218340.4 | protein_coding | 4/4 | chrX | 46878371 | |||||||
| chrX:46878376 | C | CA | 12 | a0001c0001t0001g0020 a0001c0001t0001g0034 a0001c0001t0001g0035 others(9): Show |
13 | HG01099.hp1 HG01891.hp1 HG02129.hp1 others(10): Show |
intron_variant | MODIFIER | c.969+802dupA | RP2 | ENSG00000102218.6 | transcript | ENST00000218340.4 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chrX | 46878376 | ||||||
| chrX:46878836 | C | A | 1 | a0001c0001t0005g0172 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.970-850C>A | RP2 | ENSG00000102218.6 | transcript | ENST00000218340.4 | protein_coding | 4/4 | chrX | 46878836 | |||||||
| chrX:46879061 | G | GT | 2 | a0001c0001t0001g0018 a0001c0001t0001g0073 |
3 | HG02886.hp1 HG02922.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.970-624dupT | RP2 | ENSG00000102218.6 | transcript | ENST00000218340.4 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chrX | 46879061 | ||||||
| chrX:46879062 | T | TA | 56 | a0001c0001t0001g0010 a0001c0001t0001g0012 a0001c0001t0001g0014 others(53): Show |
63 | HG00099.hp2 HG00323.hp1 HG00408.hp1 others(60): Show |
intron_variant | MODIFIER | c.970-596dupA | RP2 | ENSG00000102218.6 | transcript | ENST00000218340.4 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chrX | 46879062 | ||||||
| chrX:46879062 | T | TAA | 68 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(65): Show |
92 | HG00099.hp1 HG00423.hp1 HG00544.hp2 others(89): Show |
intron_variant | MODIFIER | c.970-597_970-596dup others(2): Show |
RP2 | ENSG00000102218.6 | transcript | ENST00000218340.4 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chrX | 46879062 | ||||||
| chrX:46879062 | T | TAAA | 20 | a0001c0001t0001g0005 a0001c0001t0001g0023 a0001c0001t0001g0053 others(17): Show |
24 | HG00639.hp2 HG01081.hp1 HG01192.hp1 others(21): Show |
intron_variant | MODIFIER | c.970-598_970-596dup others(3): Show |
RP2 | ENSG00000102218.6 | transcript | ENST00000218340.4 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chrX | 46879062 | ||||||
| chrX:46879062 | T | TAAAA | 5 | a0001c0001t0001g0022 a0001c0001t0001g0146 a0001c0001t0001g0147 others(2): Show |
6 | HG00642.hp1 HG01175.hp2 HG02280.hp2 others(3): Show |
intron_variant | MODIFIER | c.970-599_970-596dup others(4): Show |
RP2 | ENSG00000102218.6 | transcript | ENST00000218340.4 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chrX | 46879062 | ||||||
| chrX:46879311 | G | A | 1 | a0001c0001t0009g0058 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.970-375G>A | RP2 | ENSG00000102218.6 | transcript | ENST00000218340.4 | protein_coding | 4/4 | chrX | 46879311 | |||||||
| chrX:46879313 | T | A | 1 | a0001c0003t0001g0044 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.970-373T>A | RP2 | ENSG00000102218.6 | transcript | ENST00000218340.4 | protein_coding | 4/4 | chrX | 46879313 | |||||||
| chrX:46879588 | AATAATTA others(23): Show |
A | 1 | a0001c0001t0001g0200 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.970-96_970-67delTA others(28): Show |
RP2 | ENSG00000102218.6 | transcript | ENST00000218340.4 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chrX | 46879588 | ||||||
| chrX:46879621 | C | A | 1 | a0001c0001t0001g0200 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.970-65C>A | RP2 | ENSG00000102218.6 | transcript | ENST00000218340.4 | protein_coding | 4/4 | chrX | 46879621 | |||||||
| chrX:46879624 | G | A | 1 | a0001c0001t0001g0200 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.970-62G>A | RP2 | ENSG00000102218.6 | transcript | ENST00000218340.4 | protein_coding | 4/4 | chrX | 46879624 | |||||||
| chrX:46879633 | C | A | 1 | a0001c0001t0001g0200 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.970-53C>A | RP2 | ENSG00000102218.6 | transcript | ENST00000218340.4 | protein_coding | 4/4 | chrX | 46879633 | |||||||
| chrX:46879658 | T | A | 1 | a0001c0001t0001g0200 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.970-28T>A | RP2 | ENSG00000102218.6 | transcript | ENST00000218340.4 | protein_coding | 4/4 | chrX | 46879658 |