Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 10325 |
| ensemblid | ENSG00000083750.13 |
| hgncid | 19901 |
| symbol | RRAGB |
| name | Ras related GTP binding B |
| refseq_nuc | NM_006064.5 |
| refseq_prot | NP_006055.3 |
| ensembl_nuc | ENST00000374941.9 |
| ensembl_prot | ENSP00000364077.4 |
| mane_status | MANE Select |
| chr | chrX |
| start | 55717749 |
| end | 55758774 |
| strand | + |
| ver | v1.2 |
| region | chrX:55717749-55758774 |
| region5000 | chrX:55712749-55763774 |
| regionname0 | RRAGB_chrX_55717749_55758774 |
| regionname5000 | RRAGB_chrX_55712749_55763774 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 1038 | 276 | 76 | 49 | 116 | 7 | 26 | RRAGB_chrX_55712749_55763774 | RRAGB | ATGGA others(1033): Show |
chrX | 55712749 | 55763774 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 1/1 | 2051 | 168 | 41 | 25 | 79 | 5 | 16 | RRAGB_chrX_55712749_55763774 | RRAGB | AGATG others(2046): Show |
chrX | 55712749 | 55763774 |
| a0001c0001t0002 | 0/0 | 2051 | 104 | 35 | 24 | 33 | 2 | 10 | RRAGB_chrX_55712749_55763774 | RRAGB | AGATG others(2046): Show |
chrX | 55712749 | 55763774 |
| a0001c0001t0003 | 0/0 | 2051 | 2 | 0 | 0 | 2 | 0 | 0 | RRAGB_chrX_55712749_55763774 | RRAGB | AGATG others(2046): Show |
chrX | 55712749 | 55763774 |
| a0001c0001t0004 | 0/0 | 2051 | 1 | 0 | 0 | 1 | 0 | 0 | RRAGB_chrX_55712749_55763774 | RRAGB | AGATG others(2046): Show |
chrX | 55712749 | 55763774 |
| a0001c0001t0005 | 0/0 | 2051 | 1 | 0 | 0 | 1 | 0 | 0 | RRAGB_chrX_55712749_55763774 | RRAGB | AGATG others(2046): Show |
chrX | 55712749 | 55763774 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 0/0 | 34 | 0 | 4 | 29 | 1 | 0 | RRAGB_chrX_55712749_55763774 | RRAGB | chrX | 55712749 | 55763774 |
| a0001c0001t0001g0003 | 0/0 | 8 | 0 | 0 | 8 | 0 | 0 | RRAGB_chrX_55712749_55763774 | RRAGB | chrX | 55712749 | 55763774 |
| a0001c0001t0001g0004 | 0/1 | 4 | 2 | 0 | 0 | 0 | 1 | RRAGB_chrX_55712749_55763774 | RRAGB | chrX | 55712749 | 55763774 |
| a0001c0001t0001g0005 | 0/0 | 6 | 0 | 0 | 6 | 0 | 0 | RRAGB_chrX_55712749_55763774 | RRAGB | chrX | 55712749 | 55763774 |
| a0001c0001t0001g0006 | 0/0 | 6 | 6 | 0 | 0 | 0 | 0 | RRAGB_chrX_55712749_55763774 | RRAGB | chrX | 55712749 | 55763774 |
| a0001c0001t0001g0007 | 0/0 | 5 | 0 | 0 | 4 | 1 | 0 | RRAGB_chrX_55712749_55763774 | RRAGB | chrX | 55712749 | 55763774 |
| a0001c0001t0001g0009 | 0/0 | 4 | 0 | 0 | 2 | 0 | 2 | RRAGB_chrX_55712749_55763774 | RRAGB | chrX | 55712749 | 55763774 |
| a0001c0001t0001g0010 | 0/0 | 4 | 0 | 0 | 2 | 2 | 0 | RRAGB_chrX_55712749_55763774 | RRAGB | chrX | 55712749 | 55763774 |
| a0001c0001t0001g0011 | 1/0 | 3 | 2 | 0 | 0 | 0 | 0 | RRAGB_chrX_55712749_55763774 | RRAGB | chrX | 55712749 | 55763774 |
| a0001c0001t0001g0016 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | RRAGB_chrX_55712749_55763774 | RRAGB | chrX | 55712749 | 55763774 |
| a0001c0001t0001g0018 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | RRAGB_chrX_55712749_55763774 | RRAGB | chrX | 55712749 | 55763774 |
| a0001c0001t0001g0019 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | RRAGB_chrX_55712749_55763774 | RRAGB | chrX | 55712749 | 55763774 |
| a0001c0001t0001g0020 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | RRAGB_chrX_55712749_55763774 | RRAGB | chrX | 55712749 | 55763774 |
| a0001c0001t0001g0021 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | RRAGB_chrX_55712749_55763774 | RRAGB | chrX | 55712749 | 55763774 |
| a0001c0001t0001g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RRAGB_chrX_55712749_55763774 | RRAGB | chrX | 55712749 | 55763774 |
| a0001c0001t0001g0026 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RRAGB_chrX_55712749_55763774 | RRAGB | chrX | 55712749 | 55763774 |
| a0001c0001t0001g0027 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RRAGB_chrX_55712749_55763774 | RRAGB | chrX | 55712749 | 55763774 |
| a0001c0001t0001g0028 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RRAGB_chrX_55712749_55763774 | RRAGB | chrX | 55712749 | 55763774 |
| a0001c0001t0001g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RRAGB_chrX_55712749_55763774 | RRAGB | chrX | 55712749 | 55763774 |
| a0001c0001t0001g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RRAGB_chrX_55712749_55763774 | RRAGB | chrX | 55712749 | 55763774 |
| a0001c0001t0001g0031 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RRAGB_chrX_55712749_55763774 | RRAGB | chrX | 55712749 | 55763774 |
| a0001c0001t0001g0032 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RRAGB_chrX_55712749_55763774 | RRAGB | chrX | 55712749 | 55763774 |
| a0001c0001t0001g0033 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RRAGB_chrX_55712749_55763774 | RRAGB | chrX | 55712749 | 55763774 |
| a0001c0001t0001g0034 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RRAGB_chrX_55712749_55763774 | RRAGB | chrX | 55712749 | 55763774 |
| a0001c0001t0001g0035 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RRAGB_chrX_55712749_55763774 | RRAGB | chrX | 55712749 | 55763774 |
| a0001c0001t0001g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRAGB_chrX_55712749_55763774 | RRAGB | chrX | 55712749 | 55763774 |
| a0001c0001t0001g0037 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RRAGB_chrX_55712749_55763774 | RRAGB | chrX | 55712749 | 55763774 |
| a0001c0001t0001g0038 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RRAGB_chrX_55712749_55763774 | RRAGB | chrX | 55712749 | 55763774 |
| a0001c0001t0001g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRAGB_chrX_55712749_55763774 | RRAGB | chrX | 55712749 | 55763774 |
| a0001c0001t0001g0040 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RRAGB_chrX_55712749_55763774 | RRAGB | chrX | 55712749 | 55763774 |
| a0001c0001t0001g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRAGB_chrX_55712749_55763774 | RRAGB | chrX | 55712749 | 55763774 |
| a0001c0001t0001g0042 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RRAGB_chrX_55712749_55763774 | RRAGB | chrX | 55712749 | 55763774 |
| a0001c0001t0001g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRAGB_chrX_55712749_55763774 | RRAGB | chrX | 55712749 | 55763774 |
| a0001c0001t0001g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRAGB_chrX_55712749_55763774 | RRAGB | chrX | 55712749 | 55763774 |
| a0001c0001t0001g0045 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RRAGB_chrX_55712749_55763774 | RRAGB | chrX | 55712749 | 55763774 |
| a0001c0001t0001g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRAGB_chrX_55712749_55763774 | RRAGB | chrX | 55712749 | 55763774 |
| a0001c0001t0001g0047 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RRAGB_chrX_55712749_55763774 | RRAGB | chrX | 55712749 | 55763774 |
| a0001c0001t0001g0048 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RRAGB_chrX_55712749_55763774 | RRAGB | chrX | 55712749 | 55763774 |
| a0001c0001t0001g0049 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RRAGB_chrX_55712749_55763774 | RRAGB | chrX | 55712749 | 55763774 |
| a0001c0001t0001g0050 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RRAGB_chrX_55712749_55763774 | RRAGB | chrX | 55712749 | 55763774 |
| a0001c0001t0001g0051 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RRAGB_chrX_55712749_55763774 | RRAGB | chrX | 55712749 | 55763774 |
| a0001c0001t0001g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RRAGB_chrX_55712749_55763774 | RRAGB | chrX | 55712749 | 55763774 |
| a0001c0001t0001g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRAGB_chrX_55712749_55763774 | RRAGB | chrX | 55712749 | 55763774 |
| a0001c0001t0001g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRAGB_chrX_55712749_55763774 | RRAGB | chrX | 55712749 | 55763774 |
| a0001c0001t0001g0055 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RRAGB_chrX_55712749_55763774 | RRAGB | chrX | 55712749 | 55763774 |
| a0001c0001t0001g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRAGB_chrX_55712749_55763774 | RRAGB | chrX | 55712749 | 55763774 |
| a0001c0001t0001g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRAGB_chrX_55712749_55763774 | RRAGB | chrX | 55712749 | 55763774 |
| a0001c0001t0001g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRAGB_chrX_55712749_55763774 | RRAGB | chrX | 55712749 | 55763774 |
| a0001c0001t0001g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRAGB_chrX_55712749_55763774 | RRAGB | chrX | 55712749 | 55763774 |
| a0001c0001t0001g0060 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RRAGB_chrX_55712749_55763774 | RRAGB | chrX | 55712749 | 55763774 |
| a0001c0001t0001g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRAGB_chrX_55712749_55763774 | RRAGB | chrX | 55712749 | 55763774 |
| a0001c0001t0001g0062 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RRAGB_chrX_55712749_55763774 | RRAGB | chrX | 55712749 | 55763774 |
| a0001c0001t0001g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRAGB_chrX_55712749_55763774 | RRAGB | chrX | 55712749 | 55763774 |
| a0001c0001t0001g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRAGB_chrX_55712749_55763774 | RRAGB | chrX | 55712749 | 55763774 |
| a0001c0001t0001g0067 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RRAGB_chrX_55712749_55763774 | RRAGB | chrX | 55712749 | 55763774 |
| a0001c0001t0001g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRAGB_chrX_55712749_55763774 | RRAGB | chrX | 55712749 | 55763774 |
| a0001c0001t0001g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRAGB_chrX_55712749_55763774 | RRAGB | chrX | 55712749 | 55763774 |
| a0001c0001t0001g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRAGB_chrX_55712749_55763774 | RRAGB | chrX | 55712749 | 55763774 |
| a0001c0001t0001g0071 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RRAGB_chrX_55712749_55763774 | RRAGB | chrX | 55712749 | 55763774 |
| a0001c0001t0001g0072 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RRAGB_chrX_55712749_55763774 | RRAGB | chrX | 55712749 | 55763774 |
| a0001c0001t0001g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RRAGB_chrX_55712749_55763774 | RRAGB | chrX | 55712749 | 55763774 |
| a0001c0001t0001g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRAGB_chrX_55712749_55763774 | RRAGB | chrX | 55712749 | 55763774 |
| a0001c0001t0001g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRAGB_chrX_55712749_55763774 | RRAGB | chrX | 55712749 | 55763774 |
| a0001c0001t0001g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRAGB_chrX_55712749_55763774 | RRAGB | chrX | 55712749 | 55763774 |
| a0001c0001t0001g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRAGB_chrX_55712749_55763774 | RRAGB | chrX | 55712749 | 55763774 |
| a0001c0001t0001g0078 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RRAGB_chrX_55712749_55763774 | RRAGB | chrX | 55712749 | 55763774 |
| a0001c0001t0001g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRAGB_chrX_55712749_55763774 | RRAGB | chrX | 55712749 | 55763774 |
| a0001c0001t0001g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRAGB_chrX_55712749_55763774 | RRAGB | chrX | 55712749 | 55763774 |
| a0001c0001t0001g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRAGB_chrX_55712749_55763774 | RRAGB | chrX | 55712749 | 55763774 |
| a0001c0001t0001g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRAGB_chrX_55712749_55763774 | RRAGB | chrX | 55712749 | 55763774 |
| a0001c0001t0001g0083 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RRAGB_chrX_55712749_55763774 | RRAGB | chrX | 55712749 | 55763774 |
| a0001c0001t0001g0084 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RRAGB_chrX_55712749_55763774 | RRAGB | chrX | 55712749 | 55763774 |
| a0001c0001t0001g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRAGB_chrX_55712749_55763774 | RRAGB | chrX | 55712749 | 55763774 |
| a0001c0001t0001g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RRAGB_chrX_55712749_55763774 | RRAGB | chrX | 55712749 | 55763774 |
| a0001c0001t0001g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RRAGB_chrX_55712749_55763774 | RRAGB | chrX | 55712749 | 55763774 |
| a0001c0001t0001g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RRAGB_chrX_55712749_55763774 | RRAGB | chrX | 55712749 | 55763774 |
| a0001c0001t0001g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RRAGB_chrX_55712749_55763774 | RRAGB | chrX | 55712749 | 55763774 |
| a0001c0001t0001g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RRAGB_chrX_55712749_55763774 | RRAGB | chrX | 55712749 | 55763774 |
| a0001c0001t0001g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RRAGB_chrX_55712749_55763774 | RRAGB | chrX | 55712749 | 55763774 |
| a0001c0001t0001g0093 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RRAGB_chrX_55712749_55763774 | RRAGB | chrX | 55712749 | 55763774 |
| a0001c0001t0001g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RRAGB_chrX_55712749_55763774 | RRAGB | chrX | 55712749 | 55763774 |
| a0001c0001t0001g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RRAGB_chrX_55712749_55763774 | RRAGB | chrX | 55712749 | 55763774 |
| a0001c0001t0001g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RRAGB_chrX_55712749_55763774 | RRAGB | chrX | 55712749 | 55763774 |
| a0001c0001t0001g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RRAGB_chrX_55712749_55763774 | RRAGB | chrX | 55712749 | 55763774 |
| a0001c0001t0001g0099 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RRAGB_chrX_55712749_55763774 | RRAGB | chrX | 55712749 | 55763774 |
| a0001c0001t0001g0100 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RRAGB_chrX_55712749_55763774 | RRAGB | chrX | 55712749 | 55763774 |
| a0001c0001t0001g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RRAGB_chrX_55712749_55763774 | RRAGB | chrX | 55712749 | 55763774 |
| a0001c0001t0001g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RRAGB_chrX_55712749_55763774 | RRAGB | chrX | 55712749 | 55763774 |
| a0001c0001t0001g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RRAGB_chrX_55712749_55763774 | RRAGB | chrX | 55712749 | 55763774 |
| a0001c0001t0001g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RRAGB_chrX_55712749_55763774 | RRAGB | chrX | 55712749 | 55763774 |
| a0001c0001t0001g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RRAGB_chrX_55712749_55763774 | RRAGB | chrX | 55712749 | 55763774 |
| a0001c0001t0001g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RRAGB_chrX_55712749_55763774 | RRAGB | chrX | 55712749 | 55763774 |
| a0001c0001t0001g0107 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RRAGB_chrX_55712749_55763774 | RRAGB | chrX | 55712749 | 55763774 |
| a0001c0001t0001g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RRAGB_chrX_55712749_55763774 | RRAGB | chrX | 55712749 | 55763774 |
| a0001c0001t0001g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RRAGB_chrX_55712749_55763774 | RRAGB | chrX | 55712749 | 55763774 |
| a0001c0001t0001g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RRAGB_chrX_55712749_55763774 | RRAGB | chrX | 55712749 | 55763774 |
| a0001c0001t0001g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RRAGB_chrX_55712749_55763774 | RRAGB | chrX | 55712749 | 55763774 |
| a0001c0001t0001g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RRAGB_chrX_55712749_55763774 | RRAGB | chrX | 55712749 | 55763774 |
| a0001c0001t0002g0002 | 0/0 | 14 | 1 | 6 | 6 | 1 | 0 | RRAGB_chrX_55712749_55763774 | RRAGB | chrX | 55712749 | 55763774 |
| a0001c0001t0002g0004 | 0/0 | 4 | 0 | 1 | 0 | 0 | 3 | RRAGB_chrX_55712749_55763774 | RRAGB | chrX | 55712749 | 55763774 |
| a0001c0001t0002g0008 | 0/0 | 5 | 5 | 0 | 0 | 0 | 0 | RRAGB_chrX_55712749_55763774 | RRAGB | chrX | 55712749 | 55763774 |
| a0001c0001t0002g0012 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | RRAGB_chrX_55712749_55763774 | RRAGB | chrX | 55712749 | 55763774 |
| a0001c0001t0002g0013 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | RRAGB_chrX_55712749_55763774 | RRAGB | chrX | 55712749 | 55763774 |
| a0001c0001t0002g0014 | 0/0 | 3 | 1 | 1 | 1 | 0 | 0 | RRAGB_chrX_55712749_55763774 | RRAGB | chrX | 55712749 | 55763774 |
| a0001c0001t0002g0015 | 0/0 | 3 | 0 | 1 | 2 | 0 | 0 | RRAGB_chrX_55712749_55763774 | RRAGB | chrX | 55712749 | 55763774 |
| a0001c0001t0002g0017 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | RRAGB_chrX_55712749_55763774 | RRAGB | chrX | 55712749 | 55763774 |
| a0001c0001t0002g0022 | 0/0 | 2 | 1 | 0 | 1 | 0 | 0 | RRAGB_chrX_55712749_55763774 | RRAGB | chrX | 55712749 | 55763774 |
| a0001c0001t0002g0023 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | RRAGB_chrX_55712749_55763774 | RRAGB | chrX | 55712749 | 55763774 |
| a0001c0001t0002g0024 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | RRAGB_chrX_55712749_55763774 | RRAGB | chrX | 55712749 | 55763774 |
| a0001c0001t0002g0064 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RRAGB_chrX_55712749_55763774 | RRAGB | chrX | 55712749 | 55763774 |
| a0001c0001t0002g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RRAGB_chrX_55712749_55763774 | RRAGB | chrX | 55712749 | 55763774 |
| a0001c0001t0002g0094 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RRAGB_chrX_55712749_55763774 | RRAGB | chrX | 55712749 | 55763774 |
| a0001c0001t0002g0113 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RRAGB_chrX_55712749_55763774 | RRAGB | chrX | 55712749 | 55763774 |
| a0001c0001t0002g0114 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RRAGB_chrX_55712749_55763774 | RRAGB | chrX | 55712749 | 55763774 |
| a0001c0001t0002g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RRAGB_chrX_55712749_55763774 | RRAGB | chrX | 55712749 | 55763774 |
| a0001c0001t0002g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RRAGB_chrX_55712749_55763774 | RRAGB | chrX | 55712749 | 55763774 |
| a0001c0001t0002g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RRAGB_chrX_55712749_55763774 | RRAGB | chrX | 55712749 | 55763774 |
| a0001c0001t0002g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RRAGB_chrX_55712749_55763774 | RRAGB | chrX | 55712749 | 55763774 |
| a0001c0001t0002g0119 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RRAGB_chrX_55712749_55763774 | RRAGB | chrX | 55712749 | 55763774 |
| a0001c0001t0002g0120 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RRAGB_chrX_55712749_55763774 | RRAGB | chrX | 55712749 | 55763774 |
| a0001c0001t0002g0121 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RRAGB_chrX_55712749_55763774 | RRAGB | chrX | 55712749 | 55763774 |
| a0001c0001t0002g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RRAGB_chrX_55712749_55763774 | RRAGB | chrX | 55712749 | 55763774 |
| a0001c0001t0002g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RRAGB_chrX_55712749_55763774 | RRAGB | chrX | 55712749 | 55763774 |
| a0001c0001t0002g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RRAGB_chrX_55712749_55763774 | RRAGB | chrX | 55712749 | 55763774 |
| a0001c0001t0002g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RRAGB_chrX_55712749_55763774 | RRAGB | chrX | 55712749 | 55763774 |
| a0001c0001t0002g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RRAGB_chrX_55712749_55763774 | RRAGB | chrX | 55712749 | 55763774 |
| a0001c0001t0002g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RRAGB_chrX_55712749_55763774 | RRAGB | chrX | 55712749 | 55763774 |
| a0001c0001t0002g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RRAGB_chrX_55712749_55763774 | RRAGB | chrX | 55712749 | 55763774 |
| a0001c0001t0002g0129 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RRAGB_chrX_55712749_55763774 | RRAGB | chrX | 55712749 | 55763774 |
| a0001c0001t0002g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRAGB_chrX_55712749_55763774 | RRAGB | chrX | 55712749 | 55763774 |
| a0001c0001t0002g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRAGB_chrX_55712749_55763774 | RRAGB | chrX | 55712749 | 55763774 |
| a0001c0001t0002g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RRAGB_chrX_55712749_55763774 | RRAGB | chrX | 55712749 | 55763774 |
| a0001c0001t0002g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRAGB_chrX_55712749_55763774 | RRAGB | chrX | 55712749 | 55763774 |
| a0001c0001t0002g0134 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RRAGB_chrX_55712749_55763774 | RRAGB | chrX | 55712749 | 55763774 |
| a0001c0001t0002g0135 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RRAGB_chrX_55712749_55763774 | RRAGB | chrX | 55712749 | 55763774 |
| a0001c0001t0002g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRAGB_chrX_55712749_55763774 | RRAGB | chrX | 55712749 | 55763774 |
| a0001c0001t0002g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRAGB_chrX_55712749_55763774 | RRAGB | chrX | 55712749 | 55763774 |
| a0001c0001t0002g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRAGB_chrX_55712749_55763774 | RRAGB | chrX | 55712749 | 55763774 |
| a0001c0001t0002g0139 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RRAGB_chrX_55712749_55763774 | RRAGB | chrX | 55712749 | 55763774 |
| a0001c0001t0002g0140 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RRAGB_chrX_55712749_55763774 | RRAGB | chrX | 55712749 | 55763774 |
| a0001c0001t0002g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRAGB_chrX_55712749_55763774 | RRAGB | chrX | 55712749 | 55763774 |
| a0001c0001t0002g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRAGB_chrX_55712749_55763774 | RRAGB | chrX | 55712749 | 55763774 |
| a0001c0001t0002g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRAGB_chrX_55712749_55763774 | RRAGB | chrX | 55712749 | 55763774 |
| a0001c0001t0002g0144 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RRAGB_chrX_55712749_55763774 | RRAGB | chrX | 55712749 | 55763774 |
| a0001c0001t0002g0145 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RRAGB_chrX_55712749_55763774 | RRAGB | chrX | 55712749 | 55763774 |
| a0001c0001t0002g0146 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RRAGB_chrX_55712749_55763774 | RRAGB | chrX | 55712749 | 55763774 |
| a0001c0001t0002g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRAGB_chrX_55712749_55763774 | RRAGB | chrX | 55712749 | 55763774 |
| a0001c0001t0002g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRAGB_chrX_55712749_55763774 | RRAGB | chrX | 55712749 | 55763774 |
| a0001c0001t0002g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRAGB_chrX_55712749_55763774 | RRAGB | chrX | 55712749 | 55763774 |
| a0001c0001t0002g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRAGB_chrX_55712749_55763774 | RRAGB | chrX | 55712749 | 55763774 |
| a0001c0001t0002g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRAGB_chrX_55712749_55763774 | RRAGB | chrX | 55712749 | 55763774 |
| a0001c0001t0002g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRAGB_chrX_55712749_55763774 | RRAGB | chrX | 55712749 | 55763774 |
| a0001c0001t0002g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRAGB_chrX_55712749_55763774 | RRAGB | chrX | 55712749 | 55763774 |
| a0001c0001t0002g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRAGB_chrX_55712749_55763774 | RRAGB | chrX | 55712749 | 55763774 |
| a0001c0001t0002g0156 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RRAGB_chrX_55712749_55763774 | RRAGB | chrX | 55712749 | 55763774 |
| a0001c0001t0002g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRAGB_chrX_55712749_55763774 | RRAGB | chrX | 55712749 | 55763774 |
| a0001c0001t0002g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRAGB_chrX_55712749_55763774 | RRAGB | chrX | 55712749 | 55763774 |
| a0001c0001t0002g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRAGB_chrX_55712749_55763774 | RRAGB | chrX | 55712749 | 55763774 |
| a0001c0001t0002g0160 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RRAGB_chrX_55712749_55763774 | RRAGB | chrX | 55712749 | 55763774 |
| a0001c0001t0002g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRAGB_chrX_55712749_55763774 | RRAGB | chrX | 55712749 | 55763774 |
| a0001c0001t0002g0164 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RRAGB_chrX_55712749_55763774 | RRAGB | chrX | 55712749 | 55763774 |
| a0001c0001t0002g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RRAGB_chrX_55712749_55763774 | RRAGB | chrX | 55712749 | 55763774 |
| a0001c0001t0002g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RRAGB_chrX_55712749_55763774 | RRAGB | chrX | 55712749 | 55763774 |
| a0001c0001t0002g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RRAGB_chrX_55712749_55763774 | RRAGB | chrX | 55712749 | 55763774 |
| a0001c0001t0002g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RRAGB_chrX_55712749_55763774 | RRAGB | chrX | 55712749 | 55763774 |
| a0001c0001t0002g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RRAGB_chrX_55712749_55763774 | RRAGB | chrX | 55712749 | 55763774 |
| a0001c0001t0002g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RRAGB_chrX_55712749_55763774 | RRAGB | chrX | 55712749 | 55763774 |
| a0001c0001t0002g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RRAGB_chrX_55712749_55763774 | RRAGB | chrX | 55712749 | 55763774 |
| a0001c0001t0002g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRAGB_chrX_55712749_55763774 | RRAGB | chrX | 55712749 | 55763774 |
| a0001c0001t0002g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RRAGB_chrX_55712749_55763774 | RRAGB | chrX | 55712749 | 55763774 |
| a0001c0001t0003g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRAGB_chrX_55712749_55763774 | RRAGB | chrX | 55712749 | 55763774 |
| a0001c0001t0003g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRAGB_chrX_55712749_55763774 | RRAGB | chrX | 55712749 | 55763774 |
| a0001c0001t0004g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRAGB_chrX_55712749_55763774 | RRAGB | chrX | 55712749 | 55763774 |
| a0001c0001t0005g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RRAGB_chrX_55712749_55763774 | RRAGB | chrX | 55712749 | 55763774 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00140 | hp1 | a0001 | c0001 | t0002 | g0156 | EUR | GBR | RRAGB_chrX_55712749_55763774 | RRAGB | chrX | 55712749 | 55763774 |
| HG00280 | hp1 | a0001 | c0001 | t0001 | g0040 | EUR | FIN | RRAGB_chrX_55712749_55763774 | RRAGB | chrX | 55712749 | 55763774 |
| HG00423 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | CHS | RRAGB_chrX_55712749_55763774 | RRAGB | chrX | 55712749 | 55763774 |
| HG00423 | hp2 | a0001 | c0001 | t0002 | g0163 | EAS | CHS | RRAGB_chrX_55712749_55763774 | RRAGB | chrX | 55712749 | 55763774 |
| HG00544 | hp1 | a0001 | c0001 | t0002 | g0131 | EAS | CHS | RRAGB_chrX_55712749_55763774 | RRAGB | chrX | 55712749 | 55763774 |
| HG00544 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | RRAGB_chrX_55712749_55763774 | RRAGB | chrX | 55712749 | 55763774 |
| HG00609 | hp1 | a0001 | c0001 | t0001 | g0039 | EAS | CHS | RRAGB_chrX_55712749_55763774 | RRAGB | chrX | 55712749 | 55763774 |
| HG00621 | hp1 | a0001 | c0001 | t0002 | g0137 | EAS | CHS | RRAGB_chrX_55712749_55763774 | RRAGB | chrX | 55712749 | 55763774 |
| HG00642 | hp1 | a0001 | c0001 | t0001 | g0100 | AMR | PUR | RRAGB_chrX_55712749_55763774 | RRAGB | chrX | 55712749 | 55763774 |
| HG00673 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | CHS | RRAGB_chrX_55712749_55763774 | RRAGB | chrX | 55712749 | 55763774 |
| HG00733 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | RRAGB_chrX_55712749_55763774 | RRAGB | chrX | 55712749 | 55763774 |
| HG00733 | hp2 | a0001 | c0001 | t0001 | g0093 | AMR | PUR | RRAGB_chrX_55712749_55763774 | RRAGB | chrX | 55712749 | 55763774 |
| HG00735 | hp1 | a0001 | c0001 | t0001 | g0099 | AMR | PUR | RRAGB_chrX_55712749_55763774 | RRAGB | chrX | 55712749 | 55763774 |
| HG00735 | hp2 | a0001 | c0001 | t0001 | g0034 | AMR | PUR | RRAGB_chrX_55712749_55763774 | RRAGB | chrX | 55712749 | 55763774 |
| HG00738 | hp1 | a0001 | c0001 | t0002 | g0119 | AMR | PUR | RRAGB_chrX_55712749_55763774 | RRAGB | chrX | 55712749 | 55763774 |
| HG01069 | hp1 | a0001 | c0001 | t0002 | g0002 | AMR | PUR | RRAGB_chrX_55712749_55763774 | RRAGB | chrX | 55712749 | 55763774 |
| HG01071 | hp1 | a0001 | c0001 | t0001 | g0045 | AMR | PUR | RRAGB_chrX_55712749_55763774 | RRAGB | chrX | 55712749 | 55763774 |
| HG01071 | hp2 | a0001 | c0001 | t0002 | g0002 | AMR | PUR | RRAGB_chrX_55712749_55763774 | RRAGB | chrX | 55712749 | 55763774 |
| HG01074 | hp1 | a0001 | c0001 | t0001 | g0050 | AMR | PUR | RRAGB_chrX_55712749_55763774 | RRAGB | chrX | 55712749 | 55763774 |
| HG01081 | hp1 | a0001 | c0001 | t0002 | g0121 | AMR | PUR | RRAGB_chrX_55712749_55763774 | RRAGB | chrX | 55712749 | 55763774 |
| HG01081 | hp2 | a0001 | c0001 | t0001 | g0035 | AMR | PUR | RRAGB_chrX_55712749_55763774 | RRAGB | chrX | 55712749 | 55763774 |
| HG01099 | hp1 | a0001 | c0001 | t0002 | g0164 | AMR | PUR | RRAGB_chrX_55712749_55763774 | RRAGB | chrX | 55712749 | 55763774 |
| HG01106 | hp1 | a0001 | c0001 | t0001 | g0031 | AMR | PUR | RRAGB_chrX_55712749_55763774 | RRAGB | chrX | 55712749 | 55763774 |
| HG01109 | hp1 | a0001 | c0001 | t0002 | g0004 | AMR | PUR | RRAGB_chrX_55712749_55763774 | RRAGB | chrX | 55712749 | 55763774 |
| HG01167 | hp1 | a0001 | c0001 | t0002 | g0114 | AMR | PUR | RRAGB_chrX_55712749_55763774 | RRAGB | chrX | 55712749 | 55763774 |
| HG01168 | hp1 | a0001 | c0001 | t0002 | g0023 | AMR | PUR | RRAGB_chrX_55712749_55763774 | RRAGB | chrX | 55712749 | 55763774 |
| HG01168 | hp2 | a0001 | c0001 | t0001 | g0047 | AMR | PUR | RRAGB_chrX_55712749_55763774 | RRAGB | chrX | 55712749 | 55763774 |
| HG01169 | hp1 | a0001 | c0001 | t0002 | g0113 | AMR | PUR | RRAGB_chrX_55712749_55763774 | RRAGB | chrX | 55712749 | 55763774 |
| HG01169 | hp2 | a0001 | c0001 | t0002 | g0023 | AMR | PUR | RRAGB_chrX_55712749_55763774 | RRAGB | chrX | 55712749 | 55763774 |
| HG01175 | hp1 | a0001 | c0001 | t0001 | g0101 | AMR | PUR | RRAGB_chrX_55712749_55763774 | RRAGB | chrX | 55712749 | 55763774 |
| HG01175 | hp2 | a0001 | c0001 | t0001 | g0055 | AMR | PUR | RRAGB_chrX_55712749_55763774 | RRAGB | chrX | 55712749 | 55763774 |
| HG01192 | hp1 | a0001 | c0001 | t0002 | g0145 | AMR | PUR | RRAGB_chrX_55712749_55763774 | RRAGB | chrX | 55712749 | 55763774 |
| HG01243 | hp1 | a0001 | c0001 | t0001 | g0018 | AMR | PUR | RRAGB_chrX_55712749_55763774 | RRAGB | chrX | 55712749 | 55763774 |
| HG01255 | hp1 | a0001 | c0001 | t0001 | g0107 | AMR | CLM | RRAGB_chrX_55712749_55763774 | RRAGB | chrX | 55712749 | 55763774 |
| HG01256 | hp1 | a0001 | c0001 | t0001 | g0078 | AMR | CLM | RRAGB_chrX_55712749_55763774 | RRAGB | chrX | 55712749 | 55763774 |
| HG01257 | hp1 | a0001 | c0001 | t0002 | g0017 | AMR | CLM | RRAGB_chrX_55712749_55763774 | RRAGB | chrX | 55712749 | 55763774 |
| HG01257 | hp2 | a0001 | c0001 | t0002 | g0024 | AMR | CLM | RRAGB_chrX_55712749_55763774 | RRAGB | chrX | 55712749 | 55763774 |
| HG01258 | hp1 | a0001 | c0001 | t0002 | g0017 | AMR | CLM | RRAGB_chrX_55712749_55763774 | RRAGB | chrX | 55712749 | 55763774 |
| HG01261 | hp1 | a0001 | c0001 | t0001 | g0027 | AMR | CLM | RRAGB_chrX_55712749_55763774 | RRAGB | chrX | 55712749 | 55763774 |
| HG01358 | hp1 | a0001 | c0001 | t0002 | g0134 | AMR | CLM | RRAGB_chrX_55712749_55763774 | RRAGB | chrX | 55712749 | 55763774 |
| HG01433 | hp1 | a0001 | c0001 | t0002 | g0160 | AMR | CLM | RRAGB_chrX_55712749_55763774 | RRAGB | chrX | 55712749 | 55763774 |
| HG01496 | hp1 | a0001 | c0001 | t0001 | g0026 | AMR | CLM | RRAGB_chrX_55712749_55763774 | RRAGB | chrX | 55712749 | 55763774 |
| HG01496 | hp2 | a0001 | c0001 | t0002 | g0064 | AMR | CLM | RRAGB_chrX_55712749_55763774 | RRAGB | chrX | 55712749 | 55763774 |
| HG01515 | hp1 | a0001 | c0001 | t0001 | g0001 | EUR | IBS | RRAGB_chrX_55712749_55763774 | RRAGB | chrX | 55712749 | 55763774 |
| HG01517 | hp1 | a0001 | c0001 | t0001 | g0010 | EUR | IBS | RRAGB_chrX_55712749_55763774 | RRAGB | chrX | 55712749 | 55763774 |
| HG01517 | hp2 | a0001 | c0001 | t0002 | g0002 | EUR | IBS | RRAGB_chrX_55712749_55763774 | RRAGB | chrX | 55712749 | 55763774 |
| HG01884 | hp1 | a0001 | c0001 | t0001 | g0092 | AFR | ACB | RRAGB_chrX_55712749_55763774 | RRAGB | chrX | 55712749 | 55763774 |
| HG01884 | hp2 | a0001 | c0001 | t0001 | g0052 | AFR | ACB | RRAGB_chrX_55712749_55763774 | RRAGB | chrX | 55712749 | 55763774 |
| HG01891 | hp1 | a0001 | c0001 | t0001 | g0006 | AFR | ACB | RRAGB_chrX_55712749_55763774 | RRAGB | chrX | 55712749 | 55763774 |
| HG01891 | hp2 | a0001 | c0001 | t0002 | g0002 | AFR | ACB | RRAGB_chrX_55712749_55763774 | RRAGB | chrX | 55712749 | 55763774 |
| HG01928 | hp1 | a0001 | c0001 | t0002 | g0014 | AMR | PEL | RRAGB_chrX_55712749_55763774 | RRAGB | chrX | 55712749 | 55763774 |
| HG01934 | hp1 | a0001 | c0001 | t0001 | g0073 | AMR | PEL | RRAGB_chrX_55712749_55763774 | RRAGB | chrX | 55712749 | 55763774 |
| HG01943 | hp1 | a0001 | c0001 | t0002 | g0002 | AMR | PEL | RRAGB_chrX_55712749_55763774 | RRAGB | chrX | 55712749 | 55763774 |
| HG01952 | hp1 | a0001 | c0001 | t0001 | g0067 | AMR | PEL | RRAGB_chrX_55712749_55763774 | RRAGB | chrX | 55712749 | 55763774 |
| HG01975 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | RRAGB_chrX_55712749_55763774 | RRAGB | chrX | 55712749 | 55763774 |
| HG01975 | hp2 | a0001 | c0001 | t0002 | g0120 | AMR | PEL | RRAGB_chrX_55712749_55763774 | RRAGB | chrX | 55712749 | 55763774 |
| HG02004 | hp1 | a0001 | c0001 | t0002 | g0002 | AMR | PEL | RRAGB_chrX_55712749_55763774 | RRAGB | chrX | 55712749 | 55763774 |
| HG02004 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | RRAGB_chrX_55712749_55763774 | RRAGB | chrX | 55712749 | 55763774 |
| HG02015 | hp1 | a0001 | c0001 | t0001 | g0046 | EAS | KHV | RRAGB_chrX_55712749_55763774 | RRAGB | chrX | 55712749 | 55763774 |
| HG02027 | hp1 | a0001 | c0001 | t0002 | g0133 | EAS | KHV | RRAGB_chrX_55712749_55763774 | RRAGB | chrX | 55712749 | 55763774 |
| HG02040 | hp1 | a0001 | c0001 | t0002 | g0149 | EAS | KHV | RRAGB_chrX_55712749_55763774 | RRAGB | chrX | 55712749 | 55763774 |
| HG02055 | hp1 | a0001 | c0001 | t0001 | g0088 | AFR | ACB | RRAGB_chrX_55712749_55763774 | RRAGB | chrX | 55712749 | 55763774 |
| HG02056 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | KHV | RRAGB_chrX_55712749_55763774 | RRAGB | chrX | 55712749 | 55763774 |
| HG02071 | hp1 | a0001 | c0001 | t0002 | g0150 | EAS | KHV | RRAGB_chrX_55712749_55763774 | RRAGB | chrX | 55712749 | 55763774 |
| HG02074 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | KHV | RRAGB_chrX_55712749_55763774 | RRAGB | chrX | 55712749 | 55763774 |
| HG02083 | hp1 | a0001 | c0001 | t0001 | g0041 | EAS | KHV | RRAGB_chrX_55712749_55763774 | RRAGB | chrX | 55712749 | 55763774 |
| HG02129 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | KHV | RRAGB_chrX_55712749_55763774 | RRAGB | chrX | 55712749 | 55763774 |
| HG02132 | hp1 | a0001 | c0001 | t0002 | g0130 | EAS | KHV | RRAGB_chrX_55712749_55763774 | RRAGB | chrX | 55712749 | 55763774 |
| HG02135 | hp1 | a0001 | c0001 | t0001 | g0036 | EAS | KHV | RRAGB_chrX_55712749_55763774 | RRAGB | chrX | 55712749 | 55763774 |
| HG02145 | hp1 | a0001 | c0001 | t0001 | g0095 | AFR | ACB | RRAGB_chrX_55712749_55763774 | RRAGB | chrX | 55712749 | 55763774 |
| HG02148 | hp1 | a0001 | c0001 | t0002 | g0002 | AMR | PEL | RRAGB_chrX_55712749_55763774 | RRAGB | chrX | 55712749 | 55763774 |
| HG02148 | hp2 | a0001 | c0001 | t0001 | g0071 | AMR | PEL | RRAGB_chrX_55712749_55763774 | RRAGB | chrX | 55712749 | 55763774 |
| HG02155 | hp1 | a0001 | c0001 | t0004 | g0063 | EAS | CDX | RRAGB_chrX_55712749_55763774 | RRAGB | chrX | 55712749 | 55763774 |
| HG02155 | hp2 | a0001 | c0001 | t0002 | g0159 | EAS | CDX | RRAGB_chrX_55712749_55763774 | RRAGB | chrX | 55712749 | 55763774 |
| HG02165 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | CDX | RRAGB_chrX_55712749_55763774 | RRAGB | chrX | 55712749 | 55763774 |
| HG02165 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CDX | RRAGB_chrX_55712749_55763774 | RRAGB | chrX | 55712749 | 55763774 |
| HG02257 | hp1 | a0001 | c0001 | t0001 | g0011 | AFR | ACB | RRAGB_chrX_55712749_55763774 | RRAGB | chrX | 55712749 | 55763774 |
| HG02257 | hp2 | a0001 | c0001 | t0001 | g0105 | AFR | ACB | RRAGB_chrX_55712749_55763774 | RRAGB | chrX | 55712749 | 55763774 |
| HG02258 | hp1 | a0001 | c0001 | t0002 | g0171 | AFR | ACB | RRAGB_chrX_55712749_55763774 | RRAGB | chrX | 55712749 | 55763774 |
| HG02273 | hp1 | a0001 | c0001 | t0002 | g0015 | AMR | PEL | RRAGB_chrX_55712749_55763774 | RRAGB | chrX | 55712749 | 55763774 |
| HG02273 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | RRAGB_chrX_55712749_55763774 | RRAGB | chrX | 55712749 | 55763774 |
| HG02280 | hp1 | a0001 | c0001 | t0002 | g0165 | AFR | ACB | RRAGB_chrX_55712749_55763774 | RRAGB | chrX | 55712749 | 55763774 |
| HG02280 | hp2 | a0001 | c0001 | t0001 | g0089 | AFR | ACB | RRAGB_chrX_55712749_55763774 | RRAGB | chrX | 55712749 | 55763774 |
| HG02293 | hp1 | a0001 | c0001 | t0002 | g0002 | AMR | PEL | RRAGB_chrX_55712749_55763774 | RRAGB | chrX | 55712749 | 55763774 |
| HG02293 | hp2 | a0001 | c0001 | t0001 | g0028 | AMR | PEL | RRAGB_chrX_55712749_55763774 | RRAGB | chrX | 55712749 | 55763774 |
| HG02300 | hp1 | a0001 | c0001 | t0001 | g0072 | AMR | PEL | RRAGB_chrX_55712749_55763774 | RRAGB | chrX | 55712749 | 55763774 |
| HG02451 | hp1 | a0001 | c0001 | t0001 | g0086 | AFR | ACB | RRAGB_chrX_55712749_55763774 | RRAGB | chrX | 55712749 | 55763774 |
| HG02451 | hp2 | a0001 | c0001 | t0001 | g0011 | AFR | ACB | RRAGB_chrX_55712749_55763774 | RRAGB | chrX | 55712749 | 55763774 |
| HG02523 | hp1 | a0001 | c0001 | t0002 | g0024 | EAS | KHV | RRAGB_chrX_55712749_55763774 | RRAGB | chrX | 55712749 | 55763774 |
| HG02523 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | RRAGB_chrX_55712749_55763774 | RRAGB | chrX | 55712749 | 55763774 |
| HG02572 | hp1 | a0001 | c0001 | t0001 | g0112 | AFR | GWD | RRAGB_chrX_55712749_55763774 | RRAGB | chrX | 55712749 | 55763774 |
| HG02602 | hp1 | a0001 | c0001 | t0001 | g0016 | SAS | PJL | RRAGB_chrX_55712749_55763774 | RRAGB | chrX | 55712749 | 55763774 |
| HG02615 | hp1 | a0001 | c0001 | t0002 | g0132 | AFR | GWD | RRAGB_chrX_55712749_55763774 | RRAGB | chrX | 55712749 | 55763774 |
| HG02615 | hp2 | a0001 | c0001 | t0001 | g0103 | AFR | GWD | RRAGB_chrX_55712749_55763774 | RRAGB | chrX | 55712749 | 55763774 |
| HG02622 | hp1 | a0001 | c0001 | t0001 | g0006 | AFR | GWD | RRAGB_chrX_55712749_55763774 | RRAGB | chrX | 55712749 | 55763774 |
| HG02622 | hp2 | a0001 | c0001 | t0002 | g0170 | AFR | GWD | RRAGB_chrX_55712749_55763774 | RRAGB | chrX | 55712749 | 55763774 |
| HG02630 | hp1 | a0001 | c0001 | t0001 | g0006 | AFR | GWD | RRAGB_chrX_55712749_55763774 | RRAGB | chrX | 55712749 | 55763774 |
| HG02630 | hp2 | a0001 | c0001 | t0001 | g0090 | AFR | GWD | RRAGB_chrX_55712749_55763774 | RRAGB | chrX | 55712749 | 55763774 |
| HG02647 | hp1 | a0001 | c0001 | t0002 | g0118 | AFR | GWD | RRAGB_chrX_55712749_55763774 | RRAGB | chrX | 55712749 | 55763774 |
| HG02683 | hp1 | a0001 | c0001 | t0002 | g0129 | SAS | PJL | RRAGB_chrX_55712749_55763774 | RRAGB | chrX | 55712749 | 55763774 |
| HG02683 | hp2 | a0001 | c0001 | t0001 | g0004 | SAS | PJL | RRAGB_chrX_55712749_55763774 | RRAGB | chrX | 55712749 | 55763774 |
| HG02698 | hp1 | a0001 | c0001 | t0001 | g0049 | SAS | PJL | RRAGB_chrX_55712749_55763774 | RRAGB | chrX | 55712749 | 55763774 |
| HG02717 | hp1 | a0001 | c0001 | t0002 | g0126 | AFR | GWD | RRAGB_chrX_55712749_55763774 | RRAGB | chrX | 55712749 | 55763774 |
| HG02735 | hp1 | a0001 | c0001 | t0001 | g0042 | SAS | PJL | RRAGB_chrX_55712749_55763774 | RRAGB | chrX | 55712749 | 55763774 |
| HG02738 | hp1 | a0001 | c0001 | t0001 | g0083 | SAS | PJL | RRAGB_chrX_55712749_55763774 | RRAGB | chrX | 55712749 | 55763774 |
| HG02809 | hp1 | a0001 | c0001 | t0002 | g0012 | AFR | GWD | RRAGB_chrX_55712749_55763774 | RRAGB | chrX | 55712749 | 55763774 |
| HG02809 | hp2 | a0001 | c0001 | t0001 | g0021 | AFR | GWD | RRAGB_chrX_55712749_55763774 | RRAGB | chrX | 55712749 | 55763774 |
| HG02818 | hp1 | a0001 | c0001 | t0002 | g0122 | AFR | GWD | RRAGB_chrX_55712749_55763774 | RRAGB | chrX | 55712749 | 55763774 |
| HG02818 | hp2 | a0001 | c0001 | t0002 | g0116 | AFR | GWD | RRAGB_chrX_55712749_55763774 | RRAGB | chrX | 55712749 | 55763774 |
| HG02886 | hp1 | a0001 | c0001 | t0002 | g0008 | AFR | GWD | RRAGB_chrX_55712749_55763774 | RRAGB | chrX | 55712749 | 55763774 |
| HG02886 | hp2 | a0001 | c0001 | t0001 | g0004 | AFR | GWD | RRAGB_chrX_55712749_55763774 | RRAGB | chrX | 55712749 | 55763774 |
| HG02895 | hp1 | a0001 | c0001 | t0001 | g0018 | AFR | GWD | RRAGB_chrX_55712749_55763774 | RRAGB | chrX | 55712749 | 55763774 |
| HG02896 | hp1 | a0001 | c0001 | t0002 | g0128 | AFR | GWD | RRAGB_chrX_55712749_55763774 | RRAGB | chrX | 55712749 | 55763774 |
| HG02896 | hp2 | a0001 | c0001 | t0001 | g0006 | AFR | GWD | RRAGB_chrX_55712749_55763774 | RRAGB | chrX | 55712749 | 55763774 |
| HG02922 | hp1 | a0001 | c0001 | t0001 | g0097 | AFR | ESN | RRAGB_chrX_55712749_55763774 | RRAGB | chrX | 55712749 | 55763774 |
| HG02922 | hp2 | a0001 | c0001 | t0002 | g0008 | AFR | ESN | RRAGB_chrX_55712749_55763774 | RRAGB | chrX | 55712749 | 55763774 |
| HG02965 | hp1 | a0001 | c0001 | t0001 | g0019 | AFR | ESN | RRAGB_chrX_55712749_55763774 | RRAGB | chrX | 55712749 | 55763774 |
| HG02970 | hp1 | a0001 | c0001 | t0002 | g0166 | AFR | ESN | RRAGB_chrX_55712749_55763774 | RRAGB | chrX | 55712749 | 55763774 |
| HG02970 | hp2 | a0001 | c0001 | t0001 | g0111 | AFR | ESN | RRAGB_chrX_55712749_55763774 | RRAGB | chrX | 55712749 | 55763774 |
| HG02976 | hp1 | a0001 | c0001 | t0001 | g0110 | AFR | ESN | RRAGB_chrX_55712749_55763774 | RRAGB | chrX | 55712749 | 55763774 |
| HG02976 | hp2 | a0001 | c0001 | t0002 | g0013 | AFR | ESN | RRAGB_chrX_55712749_55763774 | RRAGB | chrX | 55712749 | 55763774 |
| HG03017 | hp1 | a0001 | c0001 | t0001 | g0048 | SAS | PJL | RRAGB_chrX_55712749_55763774 | RRAGB | chrX | 55712749 | 55763774 |
| HG03041 | hp1 | a0001 | c0001 | t0002 | g0022 | AFR | GWD | RRAGB_chrX_55712749_55763774 | RRAGB | chrX | 55712749 | 55763774 |
| HG03041 | hp2 | a0001 | c0001 | t0001 | g0006 | AFR | GWD | RRAGB_chrX_55712749_55763774 | RRAGB | chrX | 55712749 | 55763774 |
| HG03098 | hp1 | a0001 | c0001 | t0002 | g0115 | AFR | MSL | RRAGB_chrX_55712749_55763774 | RRAGB | chrX | 55712749 | 55763774 |
| HG03130 | hp1 | a0001 | c0001 | t0002 | g0168 | AFR | ESN | RRAGB_chrX_55712749_55763774 | RRAGB | chrX | 55712749 | 55763774 |
| HG03139 | hp1 | a0001 | c0001 | t0001 | g0098 | AFR | ESN | RRAGB_chrX_55712749_55763774 | RRAGB | chrX | 55712749 | 55763774 |
| HG03195 | hp1 | a0001 | c0001 | t0001 | g0019 | AFR | ESN | RRAGB_chrX_55712749_55763774 | RRAGB | chrX | 55712749 | 55763774 |
| HG03195 | hp2 | a0001 | c0001 | t0002 | g0012 | AFR | ESN | RRAGB_chrX_55712749_55763774 | RRAGB | chrX | 55712749 | 55763774 |
| HG03209 | hp1 | a0001 | c0001 | t0002 | g0008 | AFR | MSL | RRAGB_chrX_55712749_55763774 | RRAGB | chrX | 55712749 | 55763774 |
| HG03225 | hp1 | a0001 | c0001 | t0002 | g0008 | AFR | MSL | RRAGB_chrX_55712749_55763774 | RRAGB | chrX | 55712749 | 55763774 |
| HG03453 | hp1 | a0001 | c0001 | t0001 | g0021 | AFR | MSL | RRAGB_chrX_55712749_55763774 | RRAGB | chrX | 55712749 | 55763774 |
| HG03453 | hp2 | a0001 | c0001 | t0002 | g0173 | AFR | MSL | RRAGB_chrX_55712749_55763774 | RRAGB | chrX | 55712749 | 55763774 |
| HG03486 | hp1 | a0001 | c0001 | t0001 | g0106 | AFR | MSL | RRAGB_chrX_55712749_55763774 | RRAGB | chrX | 55712749 | 55763774 |
| HG03486 | hp2 | a0001 | c0001 | t0001 | g0109 | AFR | MSL | RRAGB_chrX_55712749_55763774 | RRAGB | chrX | 55712749 | 55763774 |
| HG03490 | hp1 | a0001 | c0001 | t0001 | g0009 | SAS | PJL | RRAGB_chrX_55712749_55763774 | RRAGB | chrX | 55712749 | 55763774 |
| HG03492 | hp1 | a0001 | c0001 | t0001 | g0032 | SAS | PJL | RRAGB_chrX_55712749_55763774 | RRAGB | chrX | 55712749 | 55763774 |
| HG03516 | hp1 | a0001 | c0001 | t0002 | g0012 | AFR | ESN | RRAGB_chrX_55712749_55763774 | RRAGB | chrX | 55712749 | 55763774 |
| HG03516 | hp2 | a0001 | c0001 | t0001 | g0025 | AFR | ESN | RRAGB_chrX_55712749_55763774 | RRAGB | chrX | 55712749 | 55763774 |
| HG03540 | hp1 | a0001 | c0001 | t0002 | g0124 | AFR | GWD | RRAGB_chrX_55712749_55763774 | RRAGB | chrX | 55712749 | 55763774 |
| HG03540 | hp2 | a0001 | c0001 | t0001 | g0006 | AFR | GWD | RRAGB_chrX_55712749_55763774 | RRAGB | chrX | 55712749 | 55763774 |
| HG03579 | hp1 | a0001 | c0001 | t0002 | g0008 | AFR | MSL | RRAGB_chrX_55712749_55763774 | RRAGB | chrX | 55712749 | 55763774 |
| HG03654 | hp1 | a0001 | c0001 | t0001 | g0033 | SAS | PJL | RRAGB_chrX_55712749_55763774 | RRAGB | chrX | 55712749 | 55763774 |
| HG03688 | hp1 | a0001 | c0001 | t0001 | g0084 | SAS | STU | RRAGB_chrX_55712749_55763774 | RRAGB | chrX | 55712749 | 55763774 |
| HG03704 | hp1 | a0001 | c0001 | t0002 | g0140 | SAS | PJL | RRAGB_chrX_55712749_55763774 | RRAGB | chrX | 55712749 | 55763774 |
| HG03704 | hp2 | a0001 | c0001 | t0002 | g0004 | SAS | PJL | RRAGB_chrX_55712749_55763774 | RRAGB | chrX | 55712749 | 55763774 |
| HG03710 | hp1 | a0001 | c0001 | t0001 | g0037 | SAS | PJL | RRAGB_chrX_55712749_55763774 | RRAGB | chrX | 55712749 | 55763774 |
| HG03831 | hp1 | a0001 | c0001 | t0001 | g0009 | SAS | BEB | RRAGB_chrX_55712749_55763774 | RRAGB | chrX | 55712749 | 55763774 |
| HG03831 | hp2 | a0001 | c0001 | t0002 | g0094 | SAS | BEB | RRAGB_chrX_55712749_55763774 | RRAGB | chrX | 55712749 | 55763774 |
| HG03834 | hp1 | a0001 | c0001 | t0002 | g0004 | SAS | BEB | RRAGB_chrX_55712749_55763774 | RRAGB | chrX | 55712749 | 55763774 |
| HG03834 | hp2 | a0001 | c0001 | t0001 | g0060 | SAS | BEB | RRAGB_chrX_55712749_55763774 | RRAGB | chrX | 55712749 | 55763774 |
| HG03942 | hp1 | a0001 | c0001 | t0001 | g0062 | SAS | BEB | RRAGB_chrX_55712749_55763774 | RRAGB | chrX | 55712749 | 55763774 |
| HG04115 | hp1 | a0001 | c0001 | t0001 | g0051 | SAS | STU | RRAGB_chrX_55712749_55763774 | RRAGB | chrX | 55712749 | 55763774 |
| HG04184 | hp1 | a0001 | c0001 | t0002 | g0135 | SAS | BEB | RRAGB_chrX_55712749_55763774 | RRAGB | chrX | 55712749 | 55763774 |
| HG04184 | hp2 | a0001 | c0001 | t0001 | g0038 | SAS | BEB | RRAGB_chrX_55712749_55763774 | RRAGB | chrX | 55712749 | 55763774 |
| HG04199 | hp1 | a0001 | c0001 | t0002 | g0144 | SAS | STU | RRAGB_chrX_55712749_55763774 | RRAGB | chrX | 55712749 | 55763774 |
| HG04204 | hp1 | a0001 | c0001 | t0002 | g0146 | SAS | STU | RRAGB_chrX_55712749_55763774 | RRAGB | chrX | 55712749 | 55763774 |
| HG04228 | hp1 | a0001 | c0001 | t0002 | g0139 | SAS | STU | RRAGB_chrX_55712749_55763774 | RRAGB | chrX | 55712749 | 55763774 |
| NA18522 | hp1 | a0001 | c0001 | t0002 | g0013 | AFR | YRI | RRAGB_chrX_55712749_55763774 | RRAGB | chrX | 55712749 | 55763774 |
| NA18612 | hp1 | a0001 | c0001 | t0002 | g0015 | EAS | CHB | RRAGB_chrX_55712749_55763774 | RRAGB | chrX | 55712749 | 55763774 |
| NA18747 | hp1 | a0001 | c0001 | t0001 | g0043 | EAS | CHB | RRAGB_chrX_55712749_55763774 | RRAGB | chrX | 55712749 | 55763774 |
| NA18906 | hp1 | a0001 | c0001 | t0001 | g0108 | AFR | YRI | RRAGB_chrX_55712749_55763774 | RRAGB | chrX | 55712749 | 55763774 |
| NA18906 | hp2 | a0001 | c0001 | t0001 | g0104 | AFR | YRI | RRAGB_chrX_55712749_55763774 | RRAGB | chrX | 55712749 | 55763774 |
| NA18939 | hp1 | a0001 | c0001 | t0002 | g0136 | EAS | JPT | RRAGB_chrX_55712749_55763774 | RRAGB | chrX | 55712749 | 55763774 |
| NA18939 | hp2 | a0001 | c0001 | t0001 | g0054 | EAS | JPT | RRAGB_chrX_55712749_55763774 | RRAGB | chrX | 55712749 | 55763774 |
| NA18940 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | RRAGB_chrX_55712749_55763774 | RRAGB | chrX | 55712749 | 55763774 |
| NA18942 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | RRAGB_chrX_55712749_55763774 | RRAGB | chrX | 55712749 | 55763774 |
| NA18942 | hp2 | a0001 | c0001 | t0002 | g0022 | EAS | JPT | RRAGB_chrX_55712749_55763774 | RRAGB | chrX | 55712749 | 55763774 |
| NA18943 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | RRAGB_chrX_55712749_55763774 | RRAGB | chrX | 55712749 | 55763774 |
| NA18944 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | RRAGB_chrX_55712749_55763774 | RRAGB | chrX | 55712749 | 55763774 |
| NA18945 | hp1 | a0001 | c0001 | t0001 | g0068 | EAS | JPT | RRAGB_chrX_55712749_55763774 | RRAGB | chrX | 55712749 | 55763774 |
| NA18946 | hp1 | a0001 | c0001 | t0003 | g0162 | EAS | JPT | RRAGB_chrX_55712749_55763774 | RRAGB | chrX | 55712749 | 55763774 |
| NA18946 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | RRAGB_chrX_55712749_55763774 | RRAGB | chrX | 55712749 | 55763774 |
| NA18947 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | RRAGB_chrX_55712749_55763774 | RRAGB | chrX | 55712749 | 55763774 |
| NA18947 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | RRAGB_chrX_55712749_55763774 | RRAGB | chrX | 55712749 | 55763774 |
| NA18948 | hp1 | a0001 | c0001 | t0002 | g0015 | EAS | JPT | RRAGB_chrX_55712749_55763774 | RRAGB | chrX | 55712749 | 55763774 |
| NA18950 | hp1 | a0001 | c0001 | t0001 | g0066 | EAS | JPT | RRAGB_chrX_55712749_55763774 | RRAGB | chrX | 55712749 | 55763774 |
| NA18950 | hp2 | a0001 | c0001 | t0002 | g0138 | EAS | JPT | RRAGB_chrX_55712749_55763774 | RRAGB | chrX | 55712749 | 55763774 |
| NA18951 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | RRAGB_chrX_55712749_55763774 | RRAGB | chrX | 55712749 | 55763774 |
| NA18951 | hp2 | a0001 | c0001 | t0001 | g0069 | EAS | JPT | RRAGB_chrX_55712749_55763774 | RRAGB | chrX | 55712749 | 55763774 |
| NA18952 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | RRAGB_chrX_55712749_55763774 | RRAGB | chrX | 55712749 | 55763774 |
| NA18953 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | RRAGB_chrX_55712749_55763774 | RRAGB | chrX | 55712749 | 55763774 |
| NA18956 | hp1 | a0001 | c0001 | t0002 | g0153 | EAS | JPT | RRAGB_chrX_55712749_55763774 | RRAGB | chrX | 55712749 | 55763774 |
| NA18956 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | RRAGB_chrX_55712749_55763774 | RRAGB | chrX | 55712749 | 55763774 |
| NA18959 | hp1 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | RRAGB_chrX_55712749_55763774 | RRAGB | chrX | 55712749 | 55763774 |
| NA18960 | hp1 | a0001 | c0001 | t0001 | g0085 | EAS | JPT | RRAGB_chrX_55712749_55763774 | RRAGB | chrX | 55712749 | 55763774 |
| NA18962 | hp1 | a0001 | c0001 | t0001 | g0070 | EAS | JPT | RRAGB_chrX_55712749_55763774 | RRAGB | chrX | 55712749 | 55763774 |
| NA18963 | hp1 | a0001 | c0001 | t0005 | g0161 | EAS | JPT | RRAGB_chrX_55712749_55763774 | RRAGB | chrX | 55712749 | 55763774 |
| NA18963 | hp2 | a0001 | c0001 | t0001 | g0080 | EAS | JPT | RRAGB_chrX_55712749_55763774 | RRAGB | chrX | 55712749 | 55763774 |
| NA18964 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | RRAGB_chrX_55712749_55763774 | RRAGB | chrX | 55712749 | 55763774 |
| NA18964 | hp2 | a0001 | c0001 | t0002 | g0151 | EAS | JPT | RRAGB_chrX_55712749_55763774 | RRAGB | chrX | 55712749 | 55763774 |
| NA18965 | hp1 | a0001 | c0001 | t0002 | g0152 | EAS | JPT | RRAGB_chrX_55712749_55763774 | RRAGB | chrX | 55712749 | 55763774 |
| NA18966 | hp1 | a0001 | c0001 | t0002 | g0157 | EAS | JPT | RRAGB_chrX_55712749_55763774 | RRAGB | chrX | 55712749 | 55763774 |
| NA18967 | hp1 | a0001 | c0001 | t0001 | g0079 | EAS | JPT | RRAGB_chrX_55712749_55763774 | RRAGB | chrX | 55712749 | 55763774 |
| NA18969 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | RRAGB_chrX_55712749_55763774 | RRAGB | chrX | 55712749 | 55763774 |
| NA18969 | hp2 | a0001 | c0001 | t0002 | g0147 | EAS | JPT | RRAGB_chrX_55712749_55763774 | RRAGB | chrX | 55712749 | 55763774 |
| NA18970 | hp1 | a0001 | c0001 | t0001 | g0075 | EAS | JPT | RRAGB_chrX_55712749_55763774 | RRAGB | chrX | 55712749 | 55763774 |
| NA18971 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | RRAGB_chrX_55712749_55763774 | RRAGB | chrX | 55712749 | 55763774 |
| NA18973 | hp1 | a0001 | c0001 | t0003 | g0155 | EAS | JPT | RRAGB_chrX_55712749_55763774 | RRAGB | chrX | 55712749 | 55763774 |
| NA18973 | hp2 | a0001 | c0001 | t0001 | g0076 | EAS | JPT | RRAGB_chrX_55712749_55763774 | RRAGB | chrX | 55712749 | 55763774 |
| NA18974 | hp1 | a0001 | c0001 | t0001 | g0053 | EAS | JPT | RRAGB_chrX_55712749_55763774 | RRAGB | chrX | 55712749 | 55763774 |
| NA18975 | hp1 | a0001 | c0001 | t0002 | g0154 | EAS | JPT | RRAGB_chrX_55712749_55763774 | RRAGB | chrX | 55712749 | 55763774 |
| NA18975 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | RRAGB_chrX_55712749_55763774 | RRAGB | chrX | 55712749 | 55763774 |
| NA18977 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | RRAGB_chrX_55712749_55763774 | RRAGB | chrX | 55712749 | 55763774 |
| NA18982 | hp1 | a0001 | c0001 | t0002 | g0172 | EAS | JPT | RRAGB_chrX_55712749_55763774 | RRAGB | chrX | 55712749 | 55763774 |
| NA18983 | hp1 | a0001 | c0001 | t0002 | g0143 | EAS | JPT | RRAGB_chrX_55712749_55763774 | RRAGB | chrX | 55712749 | 55763774 |
| NA18984 | hp1 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | RRAGB_chrX_55712749_55763774 | RRAGB | chrX | 55712749 | 55763774 |
| NA18986 | hp1 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | RRAGB_chrX_55712749_55763774 | RRAGB | chrX | 55712749 | 55763774 |
| NA18987 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | RRAGB_chrX_55712749_55763774 | RRAGB | chrX | 55712749 | 55763774 |
| NA18987 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | RRAGB_chrX_55712749_55763774 | RRAGB | chrX | 55712749 | 55763774 |
| NA18988 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | RRAGB_chrX_55712749_55763774 | RRAGB | chrX | 55712749 | 55763774 |
| NA18989 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | RRAGB_chrX_55712749_55763774 | RRAGB | chrX | 55712749 | 55763774 |
| NA18990 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | RRAGB_chrX_55712749_55763774 | RRAGB | chrX | 55712749 | 55763774 |
| NA18994 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | RRAGB_chrX_55712749_55763774 | RRAGB | chrX | 55712749 | 55763774 |
| NA18995 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | RRAGB_chrX_55712749_55763774 | RRAGB | chrX | 55712749 | 55763774 |
| NA19000 | hp1 | a0001 | c0001 | t0001 | g0065 | EAS | JPT | RRAGB_chrX_55712749_55763774 | RRAGB | chrX | 55712749 | 55763774 |
| NA19002 | hp1 | a0001 | c0001 | t0002 | g0141 | EAS | JPT | RRAGB_chrX_55712749_55763774 | RRAGB | chrX | 55712749 | 55763774 |
| NA19002 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | RRAGB_chrX_55712749_55763774 | RRAGB | chrX | 55712749 | 55763774 |
| NA19004 | hp1 | a0001 | c0001 | t0001 | g0044 | EAS | JPT | RRAGB_chrX_55712749_55763774 | RRAGB | chrX | 55712749 | 55763774 |
| NA19005 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | RRAGB_chrX_55712749_55763774 | RRAGB | chrX | 55712749 | 55763774 |
| NA19006 | hp1 | a0001 | c0001 | t0001 | g0056 | EAS | JPT | RRAGB_chrX_55712749_55763774 | RRAGB | chrX | 55712749 | 55763774 |
| NA19007 | hp1 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | RRAGB_chrX_55712749_55763774 | RRAGB | chrX | 55712749 | 55763774 |
| NA19009 | hp1 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | RRAGB_chrX_55712749_55763774 | RRAGB | chrX | 55712749 | 55763774 |
| NA19012 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | RRAGB_chrX_55712749_55763774 | RRAGB | chrX | 55712749 | 55763774 |
| NA19030 | hp1 | a0001 | c0001 | t0001 | g0029 | AFR | LWK | RRAGB_chrX_55712749_55763774 | RRAGB | chrX | 55712749 | 55763774 |
| NA19030 | hp2 | a0001 | c0001 | t0002 | g0125 | AFR | LWK | RRAGB_chrX_55712749_55763774 | RRAGB | chrX | 55712749 | 55763774 |
| NA19043 | hp1 | a0001 | c0001 | t0001 | g0030 | AFR | LWK | RRAGB_chrX_55712749_55763774 | RRAGB | chrX | 55712749 | 55763774 |
| NA19055 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | RRAGB_chrX_55712749_55763774 | RRAGB | chrX | 55712749 | 55763774 |
| NA19056 | hp1 | a0001 | c0001 | t0001 | g0074 | EAS | JPT | RRAGB_chrX_55712749_55763774 | RRAGB | chrX | 55712749 | 55763774 |
| NA19058 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | RRAGB_chrX_55712749_55763774 | RRAGB | chrX | 55712749 | 55763774 |
| NA19060 | hp1 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | RRAGB_chrX_55712749_55763774 | RRAGB | chrX | 55712749 | 55763774 |
| NA19062 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | RRAGB_chrX_55712749_55763774 | RRAGB | chrX | 55712749 | 55763774 |
| NA19063 | hp1 | a0001 | c0001 | t0001 | g0077 | EAS | JPT | RRAGB_chrX_55712749_55763774 | RRAGB | chrX | 55712749 | 55763774 |
| NA19064 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | RRAGB_chrX_55712749_55763774 | RRAGB | chrX | 55712749 | 55763774 |
| NA19064 | hp2 | a0001 | c0001 | t0002 | g0014 | EAS | JPT | RRAGB_chrX_55712749_55763774 | RRAGB | chrX | 55712749 | 55763774 |
| NA19065 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | RRAGB_chrX_55712749_55763774 | RRAGB | chrX | 55712749 | 55763774 |
| NA19065 | hp2 | a0001 | c0001 | t0001 | g0058 | EAS | JPT | RRAGB_chrX_55712749_55763774 | RRAGB | chrX | 55712749 | 55763774 |
| NA19066 | hp1 | a0001 | c0001 | t0001 | g0059 | EAS | JPT | RRAGB_chrX_55712749_55763774 | RRAGB | chrX | 55712749 | 55763774 |
| NA19067 | hp1 | a0001 | c0001 | t0001 | g0061 | EAS | JPT | RRAGB_chrX_55712749_55763774 | RRAGB | chrX | 55712749 | 55763774 |
| NA19068 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | RRAGB_chrX_55712749_55763774 | RRAGB | chrX | 55712749 | 55763774 |
| NA19070 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | RRAGB_chrX_55712749_55763774 | RRAGB | chrX | 55712749 | 55763774 |
| NA19072 | hp1 | a0001 | c0001 | t0001 | g0082 | EAS | JPT | RRAGB_chrX_55712749_55763774 | RRAGB | chrX | 55712749 | 55763774 |
| NA19074 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | RRAGB_chrX_55712749_55763774 | RRAGB | chrX | 55712749 | 55763774 |
| NA19074 | hp2 | a0001 | c0001 | t0002 | g0148 | EAS | JPT | RRAGB_chrX_55712749_55763774 | RRAGB | chrX | 55712749 | 55763774 |
| NA19075 | hp1 | a0001 | c0001 | t0001 | g0016 | EAS | JPT | RRAGB_chrX_55712749_55763774 | RRAGB | chrX | 55712749 | 55763774 |
| NA19076 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | RRAGB_chrX_55712749_55763774 | RRAGB | chrX | 55712749 | 55763774 |
| NA19079 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | RRAGB_chrX_55712749_55763774 | RRAGB | chrX | 55712749 | 55763774 |
| NA19082 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | RRAGB_chrX_55712749_55763774 | RRAGB | chrX | 55712749 | 55763774 |
| NA19083 | hp1 | a0001 | c0001 | t0001 | g0081 | EAS | JPT | RRAGB_chrX_55712749_55763774 | RRAGB | chrX | 55712749 | 55763774 |
| NA19084 | hp1 | a0001 | c0001 | t0002 | g0158 | EAS | JPT | RRAGB_chrX_55712749_55763774 | RRAGB | chrX | 55712749 | 55763774 |
| NA19084 | hp2 | a0001 | c0001 | t0001 | g0057 | EAS | JPT | RRAGB_chrX_55712749_55763774 | RRAGB | chrX | 55712749 | 55763774 |
| NA19085 | hp1 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | RRAGB_chrX_55712749_55763774 | RRAGB | chrX | 55712749 | 55763774 |
| NA19086 | hp1 | a0001 | c0001 | t0002 | g0142 | EAS | JPT | RRAGB_chrX_55712749_55763774 | RRAGB | chrX | 55712749 | 55763774 |
| NA19088 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | RRAGB_chrX_55712749_55763774 | RRAGB | chrX | 55712749 | 55763774 |
| NA19089 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | RRAGB_chrX_55712749_55763774 | RRAGB | chrX | 55712749 | 55763774 |
| NA19091 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | RRAGB_chrX_55712749_55763774 | RRAGB | chrX | 55712749 | 55763774 |
| NA19240 | hp1 | a0001 | c0001 | t0002 | g0013 | AFR | YRI | RRAGB_chrX_55712749_55763774 | RRAGB | chrX | 55712749 | 55763774 |
| NA19240 | hp2 | a0001 | c0001 | t0002 | g0117 | AFR | YRI | RRAGB_chrX_55712749_55763774 | RRAGB | chrX | 55712749 | 55763774 |
| NA20129 | hp1 | a0001 | c0001 | t0002 | g0123 | AFR | ASW | RRAGB_chrX_55712749_55763774 | RRAGB | chrX | 55712749 | 55763774 |
| NA20129 | hp2 | a0001 | c0001 | t0001 | g0102 | AFR | ASW | RRAGB_chrX_55712749_55763774 | RRAGB | chrX | 55712749 | 55763774 |
| NA20752 | hp1 | a0001 | c0001 | t0001 | g0010 | EUR | TSI | RRAGB_chrX_55712749_55763774 | RRAGB | chrX | 55712749 | 55763774 |
| NA20805 | hp1 | a0001 | c0001 | t0001 | g0007 | EUR | TSI | RRAGB_chrX_55712749_55763774 | RRAGB | chrX | 55712749 | 55763774 |
| NA20905 | hp1 | a0001 | c0001 | t0002 | g0004 | SAS | GIH | RRAGB_chrX_55712749_55763774 | RRAGB | chrX | 55712749 | 55763774 |
| HG02109 | hp1 | a0001 | c0001 | t0002 | g0167 | AFR | ACB | RRAGB_chrX_55712749_55763774 | RRAGB | chrX | 55712749 | 55763774 |
| HG02109 | hp2 | a0001 | c0001 | t0001 | g0020 | AFR | ACB | RRAGB_chrX_55712749_55763774 | RRAGB | chrX | 55712749 | 55763774 |
| HG02486 | hp1 | a0001 | c0001 | t0001 | g0096 | AFR | ACB | RRAGB_chrX_55712749_55763774 | RRAGB | chrX | 55712749 | 55763774 |
| HG02559 | hp1 | a0001 | c0001 | t0002 | g0169 | AFR | ACB | RRAGB_chrX_55712749_55763774 | RRAGB | chrX | 55712749 | 55763774 |
| HG02559 | hp2 | a0001 | c0001 | t0002 | g0127 | AFR | ACB | RRAGB_chrX_55712749_55763774 | RRAGB | chrX | 55712749 | 55763774 |
| HG03471 | hp1 | a0001 | c0001 | t0001 | g0091 | AFR | MSL | RRAGB_chrX_55712749_55763774 | RRAGB | chrX | 55712749 | 55763774 |
| HG06807 | hp1 | a0001 | c0001 | t0001 | g0020 | AFR | USA | RRAGB_chrX_55712749_55763774 | RRAGB | chrX | 55712749 | 55763774 |
| HG06807 | hp2 | a0001 | c0001 | t0002 | g0087 | AFR | USA | RRAGB_chrX_55712749_55763774 | RRAGB | chrX | 55712749 | 55763774 |
| NA18955 | hp1 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | RRAGB_chrX_55712749_55763774 | RRAGB | chrX | 55712749 | 55763774 |
| NA21309 | hp1 | a0001 | c0001 | t0001 | g0004 | AFR | LWK | RRAGB_chrX_55712749_55763774 | RRAGB | chrX | 55712749 | 55763774 |
| NA21309 | hp2 | a0001 | c0001 | t0002 | g0014 | AFR | LWK | RRAGB_chrX_55712749_55763774 | RRAGB | chrX | 55712749 | 55763774 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0001 | g0004 | REF | REF | RRAGB_chrX_55712749_55763774 | RRAGB | chrX | 55712749 | 55763774 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0001 | g0011 | REF | REF | RRAGB_chrX_55712749_55763774 | RRAGB | chrX | 55712749 | 55763774 |
| 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 |
|---|
| 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 |
|---|
| 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:55717852 | C | G | 3 | a0001c0001t0002 a0001c0001t0003 a0001c0001t0005 |
107 | HG00140.hp1 HG00423.hp2 HG00544.hp1 others(104): Show |
5_prime_UTR_variant | MODIFIER | c.-476C>G | RRAGB | ENSG00000083750.13 | transcript | ENST00000374941.9 | protein_coding | 1/10 | 476 | chrX | 55717852 | ||||||
| chrX:55717872 | G | C | 1 | a0001c0001t0003 | 2 | NA18946.hp1 NA18973.hp1 |
5_prime_UTR_variant | MODIFIER | c.-456G>C | RRAGB | ENSG00000083750.13 | transcript | ENST00000374941.9 | protein_coding | 1/10 | 456 | chrX | 55717872 | ||||||
| chrX:55717877 | C | G | 1 | a0001c0001t0004 | 1 | HG02155.hp1 | 5_prime_UTR_variant | MODIFIER | c.-451C>G | RRAGB | ENSG00000083750.13 | transcript | ENST00000374941.9 | protein_coding | 1/10 | 451 | chrX | 55717877 | ||||||
| chrX:55718298 | T | C | 1 | a0001c0001t0005 | 1 | NA18963.hp1 | 5_prime_UTR_variant | MODIFIER | c.-30T>C | RRAGB | ENSG00000083750.13 | transcript | ENST00000374941.9 | protein_coding | 1/10 | 30 | chrX | 55718298 |
| 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:55718450 | G | T | 1 | a0001c0001t0002g0173 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.92+31G>T | RRAGB | ENSG00000083750.13 | transcript | ENST00000374941.9 | protein_coding | 1/9 | chrX | 55718450 | |||||||
| chrX:55718559 | T | C | 1 | a0001c0001t0001g0025 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.92+140T>C | RRAGB | ENSG00000083750.13 | transcript | ENST00000374941.9 | protein_coding | 1/9 | chrX | 55718559 | |||||||
| chrX:55718650 | G | A | 68 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(65): Show |
125 | HG00280.hp1 HG00423.hp1 HG00544.hp2 others(122): Show |
intron_variant | MODIFIER | c.92+231G>A | RRAGB | ENSG00000083750.13 | transcript | ENST00000374941.9 | protein_coding | 1/9 | chrX | 55718650 | |||||||
| chrX:55719570 | G | A | 1 | a0001c0001t0001g0086 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.126+223G>A | RRAGB | ENSG00000083750.13 | transcript | ENST00000374941.9 | protein_coding | 2/9 | chrX | 55719570 | |||||||
| chrX:55719828 | T | C | 1 | a0001c0001t0002g0087 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.126+481T>C | RRAGB | ENSG00000083750.13 | transcript | ENST00000374941.9 | protein_coding | 2/9 | chrX | 55719828 | |||||||
| chrX:55719993 | A | C | 71 | a0001c0001t0002g0002 a0001c0001t0002g0008 a0001c0001t0002g0012 others(68): Show |
99 | HG00140.hp1 HG00423.hp2 HG00544.hp1 others(96): Show |
intron_variant | MODIFIER | c.126+646A>C | RRAGB | ENSG00000083750.13 | transcript | ENST00000374941.9 | protein_coding | 2/9 | chrX | 55719993 | |||||||
| chrX:55720212 | G | A | 140 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(137): Show |
225 | HG00140.hp1 HG00280.hp1 HG00423.hp1 others(222): Show |
intron_variant | MODIFIER | c.126+865G>A | RRAGB | ENSG00000083750.13 | transcript | ENST00000374941.9 | protein_coding | 2/9 | chrX | 55720212 | |||||||
| chrX:55720559 | G | A | 68 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(65): Show |
125 | HG00280.hp1 HG00423.hp1 HG00544.hp2 others(122): Show |
intron_variant | MODIFIER | c.126+1212G>A | RRAGB | ENSG00000083750.13 | transcript | ENST00000374941.9 | protein_coding | 2/9 | chrX | 55720559 | |||||||
| chrX:55720663 | A | G | 1 | a0001c0001t0002g0172 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.126+1316A>G | RRAGB | ENSG00000083750.13 | transcript | ENST00000374941.9 | protein_coding | 2/9 | chrX | 55720663 | |||||||
| chrX:55720687 | CA | C | 77 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(74): Show |
135 | HG00280.hp1 HG00423.hp1 HG00544.hp2 others(132): Show |
intron_variant | MODIFIER | c.126+1356delA | RRAGB | ENSG00000083750.13 | transcript | ENST00000374941.9 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chrX | 55720687 | ||||||
| chrX:55720687 | CAA | C | 71 | a0001c0001t0001g0084 a0001c0001t0001g0085 a0001c0001t0002g0002 others(68): Show |
99 | HG00140.hp1 HG00423.hp2 HG00544.hp1 others(96): Show |
intron_variant | MODIFIER | c.126+1355_126+1356d others(4): Show |
RRAGB | ENSG00000083750.13 | transcript | ENST00000374941.9 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chrX | 55720687 | ||||||
| chrX:55720770 | G | A | 1 | a0001c0001t0001g0018 | 2 | HG01243.hp1 HG02895.hp1 |
intron_variant | MODIFIER | c.127-1416G>A | RRAGB | ENSG00000083750.13 | transcript | ENST00000374941.9 | protein_coding | 2/9 | chrX | 55720770 | |||||||
| chrX:55720803 | G | A | 8 | a0001c0001t0002g0008 a0001c0001t0002g0113 a0001c0001t0002g0114 others(5): Show |
12 | HG00738.hp1 HG01167.hp1 HG01169.hp1 others(9): Show |
intron_variant | MODIFIER | c.127-1383G>A | RRAGB | ENSG00000083750.13 | transcript | ENST00000374941.9 | protein_coding | 2/9 | chrX | 55720803 | |||||||
| chrX:55720808 | G | A | 71 | a0001c0001t0002g0002 a0001c0001t0002g0008 a0001c0001t0002g0012 others(68): Show |
99 | HG00140.hp1 HG00423.hp2 HG00544.hp1 others(96): Show |
intron_variant | MODIFIER | c.127-1378G>A | RRAGB | ENSG00000083750.13 | transcript | ENST00000374941.9 | protein_coding | 2/9 | chrX | 55720808 | |||||||
| chrX:55721284 | A | G | 71 | a0001c0001t0002g0002 a0001c0001t0002g0008 a0001c0001t0002g0012 others(68): Show |
99 | HG00140.hp1 HG00423.hp2 HG00544.hp1 others(96): Show |
intron_variant | MODIFIER | c.127-902A>G | RRAGB | ENSG00000083750.13 | transcript | ENST00000374941.9 | protein_coding | 2/9 | chrX | 55721284 | |||||||
| chrX:55721482 | A | T | 1 | a0001c0001t0002g0171 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.127-704A>T | RRAGB | ENSG00000083750.13 | transcript | ENST00000374941.9 | protein_coding | 2/9 | chrX | 55721482 | |||||||
| chrX:55721509 | C | T | 1 | a0001c0001t0001g0025 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.127-677C>T | RRAGB | ENSG00000083750.13 | transcript | ENST00000374941.9 | protein_coding | 2/9 | chrX | 55721509 | |||||||
| chrX:55721518 | A | G | 71 | a0001c0001t0002g0002 a0001c0001t0002g0008 a0001c0001t0002g0012 others(68): Show |
99 | HG00140.hp1 HG00423.hp2 HG00544.hp1 others(96): Show |
intron_variant | MODIFIER | c.127-668A>G | RRAGB | ENSG00000083750.13 | transcript | ENST00000374941.9 | protein_coding | 2/9 | chrX | 55721518 | |||||||
| chrX:55721629 | G | T | 1 | a0001c0001t0001g0086 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.127-557G>T | RRAGB | ENSG00000083750.13 | transcript | ENST00000374941.9 | protein_coding | 2/9 | chrX | 55721629 | |||||||
| chrX:55721707 | A | G | 4 | a0001c0001t0002g0167 a0001c0001t0002g0168 a0001c0001t0002g0169 others(1): Show |
4 | HG02109.hp1 HG02559.hp1 HG02622.hp2 others(1): Show |
intron_variant | MODIFIER | c.127-479A>G | RRAGB | ENSG00000083750.13 | transcript | ENST00000374941.9 | protein_coding | 2/9 | chrX | 55721707 | |||||||
| chrX:55722082 | A | G | 1 | a0001c0001t0001g0083 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.127-104A>G | RRAGB | ENSG00000083750.13 | transcript | ENST00000374941.9 | protein_coding | 2/9 | chrX | 55722082 | |||||||
| chrX:55722091 | A | G | 1 | a0001c0001t0001g0103 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.127-95A>G | RRAGB | ENSG00000083750.13 | transcript | ENST00000374941.9 | protein_coding | 2/9 | chrX | 55722091 | |||||||
| chrX:55722108 | G | C | 1 | a0001c0001t0002g0120 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.127-78G>C | RRAGB | ENSG00000083750.13 | transcript | ENST00000374941.9 | protein_coding | 2/9 | chrX | 55722108 | |||||||
| chrX:55722387 | A | G | 140 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(137): Show |
225 | HG00140.hp1 HG00280.hp1 HG00423.hp1 others(222): Show |
intron_variant | MODIFIER | c.226+102A>G | RRAGB | ENSG00000083750.13 | transcript | ENST00000374941.9 | protein_coding | 3/9 | chrX | 55722387 | |||||||
| chrX:55722467 | G | T | 71 | a0001c0001t0002g0002 a0001c0001t0002g0008 a0001c0001t0002g0012 others(68): Show |
99 | HG00140.hp1 HG00423.hp2 HG00544.hp1 others(96): Show |
intron_variant | MODIFIER | c.226+182G>T | RRAGB | ENSG00000083750.13 | transcript | ENST00000374941.9 | protein_coding | 3/9 | chrX | 55722467 | |||||||
| chrX:55722699 | A | G | 8 | a0001c0001t0002g0008 a0001c0001t0002g0113 a0001c0001t0002g0114 others(5): Show |
12 | HG00738.hp1 HG01167.hp1 HG01169.hp1 others(9): Show |
intron_variant | MODIFIER | c.226+414A>G | RRAGB | ENSG00000083750.13 | transcript | ENST00000374941.9 | protein_coding | 3/9 | chrX | 55722699 | |||||||
| chrX:55722700 | C | T | 2 | a0001c0001t0002g0165 a0001c0001t0002g0166 |
2 | HG02280.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.226+415C>T | RRAGB | ENSG00000083750.13 | transcript | ENST00000374941.9 | protein_coding | 3/9 | chrX | 55722700 | |||||||
| chrX:55722705 | G | A | 14 | a0001c0001t0002g0012 a0001c0001t0002g0013 a0001c0001t0002g0121 others(11): Show |
18 | HG01081.hp1 HG02258.hp1 HG02280.hp1 others(15): Show |
intron_variant | MODIFIER | c.226+420G>A | RRAGB | ENSG00000083750.13 | transcript | ENST00000374941.9 | protein_coding | 3/9 | chrX | 55722705 | |||||||
| chrX:55722845 | T | G | 1 | a0001c0001t0001g0088 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.226+560T>G | RRAGB | ENSG00000083750.13 | transcript | ENST00000374941.9 | protein_coding | 3/9 | chrX | 55722845 | |||||||
| chrX:55722973 | G | A | 1 | a0001c0001t0001g0025 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.226+688G>A | RRAGB | ENSG00000083750.13 | transcript | ENST00000374941.9 | protein_coding | 3/9 | chrX | 55722973 | |||||||
| chrX:55723025 | A | C | 1 | a0001c0001t0002g0164 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.226+740A>C | RRAGB | ENSG00000083750.13 | transcript | ENST00000374941.9 | protein_coding | 3/9 | chrX | 55723025 | |||||||
| chrX:55723295 | C | T | 1 | a0001c0001t0002g0128 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.226+1010C>T | RRAGB | ENSG00000083750.13 | transcript | ENST00000374941.9 | protein_coding | 3/9 | chrX | 55723295 | |||||||
| chrX:55723474 | C | T | 63 | a0001c0001t0002g0002 a0001c0001t0002g0012 a0001c0001t0002g0013 others(60): Show |
87 | HG00140.hp1 HG00423.hp2 HG00544.hp1 others(84): Show |
intron_variant | MODIFIER | c.226+1189C>T | RRAGB | ENSG00000083750.13 | transcript | ENST00000374941.9 | protein_coding | 3/9 | chrX | 55723474 | |||||||
| chrX:55723570 | T | C | 2 | a0001c0001t0001g0086 a0001c0001t0001g0103 |
2 | HG02451.hp1 HG02615.hp2 |
intron_variant | MODIFIER | c.226+1285T>C | RRAGB | ENSG00000083750.13 | transcript | ENST00000374941.9 | protein_coding | 3/9 | chrX | 55723570 | |||||||
| chrX:55723601 | A | G | 1 | a0001c0001t0002g0119 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.226+1316A>G | RRAGB | ENSG00000083750.13 | transcript | ENST00000374941.9 | protein_coding | 3/9 | chrX | 55723601 | |||||||
| chrX:55723857 | C | T | 1 | a0001c0001t0001g0102 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.226+1572C>T | RRAGB | ENSG00000083750.13 | transcript | ENST00000374941.9 | protein_coding | 3/9 | chrX | 55723857 | |||||||
| chrX:55723914 | A | G | 70 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(67): Show |
127 | HG00280.hp1 HG00423.hp1 HG00423.hp2 others(124): Show |
intron_variant | MODIFIER | c.226+1629A>G | RRAGB | ENSG00000083750.13 | transcript | ENST00000374941.9 | protein_coding | 3/9 | chrX | 55723914 | |||||||
| chrX:55724209 | T | C | 3 | a0001c0001t0001g0026 a0001c0001t0001g0027 a0001c0001t0001g0028 |
3 | HG01261.hp1 HG01496.hp1 HG02293.hp2 |
intron_variant | MODIFIER | c.226+1924T>C | RRAGB | ENSG00000083750.13 | transcript | ENST00000374941.9 | protein_coding | 3/9 | chrX | 55724209 | |||||||
| chrX:55724741 | T | C | 1 | a0001c0001t0001g0029 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.226+2456T>C | RRAGB | ENSG00000083750.13 | transcript | ENST00000374941.9 | protein_coding | 3/9 | chrX | 55724741 | |||||||
| chrX:55724920 | G | A | 173 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(170): Show |
272 | HG00140.hp1 HG00280.hp1 HG00423.hp1 others(269): Show |
intron_variant | MODIFIER | c.226+2635G>A | RRAGB | ENSG00000083750.13 | transcript | ENST00000374941.9 | protein_coding | 3/9 | chrX | 55724920 | |||||||
| chrX:55725419 | A | G | 2 | a0001c0001t0002g0113 a0001c0001t0002g0114 |
2 | HG01167.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.226+3134A>G | RRAGB | ENSG00000083750.13 | transcript | ENST00000374941.9 | protein_coding | 3/9 | chrX | 55725419 | |||||||
| chrX:55726106 | A | G | 2 | a0001c0001t0002g0113 a0001c0001t0002g0114 |
2 | HG01167.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.227-3188A>G | RRAGB | ENSG00000083750.13 | transcript | ENST00000374941.9 | protein_coding | 3/9 | chrX | 55726106 | |||||||
| chrX:55726151 | T | TA | 134 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(131): Show |
218 | HG00140.hp1 HG00280.hp1 HG00423.hp1 others(215): Show |
intron_variant | MODIFIER | c.227-3132dupA | RRAGB | ENSG00000083750.13 | transcript | ENST00000374941.9 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chrX | 55726151 | ||||||
| chrX:55726300 | T | C | 14 | a0001c0001t0002g0012 a0001c0001t0002g0013 a0001c0001t0002g0121 others(11): Show |
18 | HG01081.hp1 HG02258.hp1 HG02280.hp1 others(15): Show |
intron_variant | MODIFIER | c.227-2994T>C | RRAGB | ENSG00000083750.13 | transcript | ENST00000374941.9 | protein_coding | 3/9 | chrX | 55726300 | |||||||
| chrX:55726419 | T | C | 1 | a0001c0001t0001g0030 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.227-2875T>C | RRAGB | ENSG00000083750.13 | transcript | ENST00000374941.9 | protein_coding | 3/9 | chrX | 55726419 | |||||||
| chrX:55726510 | T | G | 1 | a0001c0001t0001g0089 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.227-2784T>G | RRAGB | ENSG00000083750.13 | transcript | ENST00000374941.9 | protein_coding | 3/9 | chrX | 55726510 | |||||||
| chrX:55726696 | T | G | 1 | a0001c0001t0002g0129 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.227-2598T>G | RRAGB | ENSG00000083750.13 | transcript | ENST00000374941.9 | protein_coding | 3/9 | chrX | 55726696 | |||||||
| chrX:55726759 | G | C | 1 | a0001c0001t0002g0130 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.227-2535G>C | RRAGB | ENSG00000083750.13 | transcript | ENST00000374941.9 | protein_coding | 3/9 | chrX | 55726759 | |||||||
| chrX:55726864 | T | C | 145 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(142): Show |
230 | HG00140.hp1 HG00280.hp1 HG00423.hp1 others(227): Show |
intron_variant | MODIFIER | c.227-2430T>C | RRAGB | ENSG00000083750.13 | transcript | ENST00000374941.9 | protein_coding | 3/9 | chrX | 55726864 | |||||||
| chrX:55726865 | C | G | 5 | a0001c0001t0001g0090 a0001c0001t0001g0104 a0001c0001t0001g0105 others(2): Show |
5 | HG01255.hp1 HG02257.hp2 HG02630.hp2 others(2): Show |
intron_variant | MODIFIER | c.227-2429C>G | RRAGB | ENSG00000083750.13 | transcript | ENST00000374941.9 | protein_coding | 3/9 | chrX | 55726865 | |||||||
| chrX:55728104 | G | A | 3 | a0001c0001t0002g0008 a0001c0001t0002g0115 a0001c0001t0002g0116 |
7 | HG02818.hp2 HG02886.hp1 HG02922.hp2 others(4): Show |
intron_variant | MODIFIER | c.227-1190G>A | RRAGB | ENSG00000083750.13 | transcript | ENST00000374941.9 | protein_coding | 3/9 | chrX | 55728104 | |||||||
| chrX:55728108 | A | G | 1 | a0001c0001t0005g0161 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.227-1186A>G | RRAGB | ENSG00000083750.13 | transcript | ENST00000374941.9 | protein_coding | 3/9 | chrX | 55728108 | |||||||
| chrX:55728148 | A | T | 1 | a0001c0001t0002g0170 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.227-1146A>T | RRAGB | ENSG00000083750.13 | transcript | ENST00000374941.9 | protein_coding | 3/9 | chrX | 55728148 | |||||||
| chrX:55728333 | C | T | 1 | a0001c0001t0002g0160 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.227-961C>T | RRAGB | ENSG00000083750.13 | transcript | ENST00000374941.9 | protein_coding | 3/9 | chrX | 55728333 | |||||||
| chrX:55728632 | G | A | 1 | a0001c0001t0001g0031 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.227-662G>A | RRAGB | ENSG00000083750.13 | transcript | ENST00000374941.9 | protein_coding | 3/9 | chrX | 55728632 | |||||||
| chrX:55728827 | G | T | 1 | a0001c0001t0002g0164 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.227-467G>T | RRAGB | ENSG00000083750.13 | transcript | ENST00000374941.9 | protein_coding | 3/9 | chrX | 55728827 | |||||||
| chrX:55728962 | G | A | 1 | a0001c0001t0001g0031 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.227-332G>A | RRAGB | ENSG00000083750.13 | transcript | ENST00000374941.9 | protein_coding | 3/9 | chrX | 55728962 | |||||||
| chrX:55729112 | G | T | 1 | a0001c0001t0001g0079 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.227-182G>T | RRAGB | ENSG00000083750.13 | transcript | ENST00000374941.9 | protein_coding | 3/9 | chrX | 55729112 | |||||||
| chrX:55729261 | A | T | 1 | a0001c0001t0001g0020 | 2 | HG02109.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.227-33A>T | RRAGB | ENSG00000083750.13 | transcript | ENST00000374941.9 | protein_coding | 3/9 | chrX | 55729261 | |||||||
| chrX:55729604 | T | A | 1 | a0001c0001t0001g0025 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.293+244T>A | RRAGB | ENSG00000083750.13 | transcript | ENST00000374941.9 | protein_coding | 4/9 | chrX | 55729604 | |||||||
| chrX:55729679 | C | G | 5 | a0001c0001t0001g0090 a0001c0001t0001g0104 a0001c0001t0001g0105 others(2): Show |
5 | HG01255.hp1 HG02257.hp2 HG02630.hp2 others(2): Show |
intron_variant | MODIFIER | c.293+319C>G | RRAGB | ENSG00000083750.13 | transcript | ENST00000374941.9 | protein_coding | 4/9 | chrX | 55729679 | |||||||
| chrX:55729834 | A | C | 1 | a0001c0001t0001g0078 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.293+474A>C | RRAGB | ENSG00000083750.13 | transcript | ENST00000374941.9 | protein_coding | 4/9 | chrX | 55729834 | |||||||
| chrX:55730015 | C | G | 1 | a0001c0001t0001g0025 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.293+655C>G | RRAGB | ENSG00000083750.13 | transcript | ENST00000374941.9 | protein_coding | 4/9 | chrX | 55730015 | |||||||
| chrX:55730424 | A | G | 1 | a0001c0001t0002g0129 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.294-940A>G | RRAGB | ENSG00000083750.13 | transcript | ENST00000374941.9 | protein_coding | 4/9 | chrX | 55730424 | |||||||
| chrX:55730454 | C | T | 1 | a0001c0001t0001g0025 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.294-910C>T | RRAGB | ENSG00000083750.13 | transcript | ENST00000374941.9 | protein_coding | 4/9 | chrX | 55730454 | |||||||
| chrX:55730574 | C | A | 1 | a0001c0001t0002g0167 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.294-790C>A | RRAGB | ENSG00000083750.13 | transcript | ENST00000374941.9 | protein_coding | 4/9 | chrX | 55730574 | |||||||
| chrX:55731303 | G | C | 1 | a0001c0001t0001g0025 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.294-61G>C | RRAGB | ENSG00000083750.13 | transcript | ENST00000374941.9 | protein_coding | 4/9 | chrX | 55731303 | |||||||
| chrX:55731311 | T | G | 140 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(137): Show |
225 | HG00140.hp1 HG00280.hp1 HG00423.hp1 others(222): Show |
intron_variant | MODIFIER | c.294-53T>G | RRAGB | ENSG00000083750.13 | transcript | ENST00000374941.9 | protein_coding | 4/9 | chrX | 55731311 | |||||||
| chrX:55731344 | A | G | 18 | a0001c0001t0001g0007 a0001c0001t0001g0065 a0001c0001t0001g0066 others(15): Show |
23 | HG01257.hp1 HG01258.hp1 HG01496.hp2 others(20): Show |
intron_variant | MODIFIER | c.294-20A>G | RRAGB | ENSG00000083750.13 | transcript | ENST00000374941.9 | protein_coding | 4/9 | chrX | 55731344 | |||||||
| chrX:55731350 | A | T | 1 | a0001c0001t0001g0025 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.294-14A>T | RRAGB | ENSG00000083750.13 | transcript | ENST00000374941.9 | protein_coding | 4/9 | chrX | 55731350 | |||||||
| chrX:55731697 | A | G | 1 | a0001c0001t0004g0063 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.516+111A>G | RRAGB | ENSG00000083750.13 | transcript | ENST00000374941.9 | protein_coding | 5/9 | chrX | 55731697 | |||||||
| chrX:55731805 | T | A | 140 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(137): Show |
225 | HG00140.hp1 HG00280.hp1 HG00423.hp1 others(222): Show |
intron_variant | MODIFIER | c.516+219T>A | RRAGB | ENSG00000083750.13 | transcript | ENST00000374941.9 | protein_coding | 5/9 | chrX | 55731805 | |||||||
| chrX:55731848 | A | T | 67 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(64): Show |
123 | HG00280.hp1 HG00423.hp1 HG00544.hp2 others(120): Show |
intron_variant | MODIFIER | c.516+262A>T | RRAGB | ENSG00000083750.13 | transcript | ENST00000374941.9 | protein_coding | 5/9 | chrX | 55731848 | |||||||
| chrX:55731935 | G | A | 1 | a0001c0001t0001g0032 | 1 | HG03492.hp1 | intron_variant | MODIFIER | c.516+349G>A | RRAGB | ENSG00000083750.13 | transcript | ENST00000374941.9 | protein_coding | 5/9 | chrX | 55731935 | |||||||
| chrX:55731975 | C | T | 67 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(64): Show |
123 | HG00280.hp1 HG00423.hp1 HG00544.hp2 others(120): Show |
intron_variant | MODIFIER | c.516+389C>T | RRAGB | ENSG00000083750.13 | transcript | ENST00000374941.9 | protein_coding | 5/9 | chrX | 55731975 | |||||||
| chrX:55731985 | A | G | 3 | a0001c0001t0002g0157 a0001c0001t0002g0158 a0001c0001t0002g0159 |
3 | HG02155.hp2 NA18966.hp1 NA19084.hp1 |
intron_variant | MODIFIER | c.516+399A>G | RRAGB | ENSG00000083750.13 | transcript | ENST00000374941.9 | protein_coding | 5/9 | chrX | 55731985 | |||||||
| chrX:55732042 | A | G | 1 | a0001c0001t0001g0025 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.516+456A>G | RRAGB | ENSG00000083750.13 | transcript | ENST00000374941.9 | protein_coding | 5/9 | chrX | 55732042 | |||||||
| chrX:55732145 | A | C | 1 | a0001c0001t0001g0025 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.516+559A>C | RRAGB | ENSG00000083750.13 | transcript | ENST00000374941.9 | protein_coding | 5/9 | chrX | 55732145 | |||||||
| chrX:55732297 | T | A | 1 | a0001c0001t0001g0080 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.516+711T>A | RRAGB | ENSG00000083750.13 | transcript | ENST00000374941.9 | protein_coding | 5/9 | chrX | 55732297 | |||||||
| chrX:55732489 | C | G | 2 | a0001c0001t0001g0100 a0001c0001t0001g0101 |
2 | HG00642.hp1 HG01175.hp1 |
intron_variant | MODIFIER | c.516+903C>G | RRAGB | ENSG00000083750.13 | transcript | ENST00000374941.9 | protein_coding | 5/9 | chrX | 55732489 | |||||||
| chrX:55732729 | C | T | 64 | a0001c0001t0002g0002 a0001c0001t0002g0012 a0001c0001t0002g0013 others(61): Show |
89 | HG00140.hp1 HG00423.hp2 HG00621.hp1 others(86): Show |
intron_variant | MODIFIER | c.516+1143C>T | RRAGB | ENSG00000083750.13 | transcript | ENST00000374941.9 | protein_coding | 5/9 | chrX | 55732729 | |||||||
| chrX:55732891 | C | T | 1 | a0001c0001t0002g0013 | 3 | HG02976.hp2 NA18522.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.516+1305C>T | RRAGB | ENSG00000083750.13 | transcript | ENST00000374941.9 | protein_coding | 5/9 | chrX | 55732891 | |||||||
| chrX:55732912 | C | G | 1 | a0001c0001t0001g0062 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.516+1326C>G | RRAGB | ENSG00000083750.13 | transcript | ENST00000374941.9 | protein_coding | 5/9 | chrX | 55732912 | |||||||
| chrX:55732979 | T | A | 1 | a0001c0001t0001g0104 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.516+1393T>A | RRAGB | ENSG00000083750.13 | transcript | ENST00000374941.9 | protein_coding | 5/9 | chrX | 55732979 | |||||||
| chrX:55733043 | G | A | 1 | a0001c0001t0002g0119 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.516+1457G>A | RRAGB | ENSG00000083750.13 | transcript | ENST00000374941.9 | protein_coding | 5/9 | chrX | 55733043 | |||||||
| chrX:55733141 | C | T | 1 | a0001c0001t0001g0099 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.516+1555C>T | RRAGB | ENSG00000083750.13 | transcript | ENST00000374941.9 | protein_coding | 5/9 | chrX | 55733141 | |||||||
| chrX:55733180 | C | G | 1 | a0001c0001t0002g0156 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.516+1594C>G | RRAGB | ENSG00000083750.13 | transcript | ENST00000374941.9 | protein_coding | 5/9 | chrX | 55733180 | |||||||
| chrX:55733497 | GT | G | 140 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(137): Show |
225 | HG00140.hp1 HG00280.hp1 HG00423.hp1 others(222): Show |
intron_variant | MODIFIER | c.516+1918delT | RRAGB | ENSG00000083750.13 | transcript | ENST00000374941.9 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chrX | 55733497 | ||||||
| chrX:55733706 | A | G | 2 | a0001c0001t0003g0155 a0001c0001t0003g0162 |
2 | NA18946.hp1 NA18973.hp1 |
intron_variant | MODIFIER | c.516+2120A>G | RRAGB | ENSG00000083750.13 | transcript | ENST00000374941.9 | protein_coding | 5/9 | chrX | 55733706 | |||||||
| chrX:55733931 | GT | G | 66 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(63): Show |
123 | HG00280.hp1 HG00423.hp1 HG00544.hp2 others(120): Show |
intron_variant | MODIFIER | c.516+2356delT | RRAGB | ENSG00000083750.13 | transcript | ENST00000374941.9 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chrX | 55733931 | ||||||
| chrX:55733958 | A | G | 140 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(137): Show |
225 | HG00140.hp1 HG00280.hp1 HG00423.hp1 others(222): Show |
intron_variant | MODIFIER | c.516+2372A>G | RRAGB | ENSG00000083750.13 | transcript | ENST00000374941.9 | protein_coding | 5/9 | chrX | 55733958 | |||||||
| chrX:55733963 | T | C | 1 | a0001c0001t0001g0030 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.516+2377T>C | RRAGB | ENSG00000083750.13 | transcript | ENST00000374941.9 | protein_coding | 5/9 | chrX | 55733963 | |||||||
| chrX:55733986 | C | T | 1 | a0001c0001t0002g0127 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.516+2400C>T | RRAGB | ENSG00000083750.13 | transcript | ENST00000374941.9 | protein_coding | 5/9 | chrX | 55733986 | |||||||
| chrX:55733994 | C | T | 2 | a0001c0001t0001g0086 a0001c0001t0001g0103 |
2 | HG02451.hp1 HG02615.hp2 |
intron_variant | MODIFIER | c.516+2408C>T | RRAGB | ENSG00000083750.13 | transcript | ENST00000374941.9 | protein_coding | 5/9 | chrX | 55733994 | |||||||
| chrX:55734032 | C | T | 3 | a0001c0001t0001g0006 a0001c0001t0001g0019 a0001c0001t0001g0098 |
9 | HG01891.hp1 HG02622.hp1 HG02630.hp1 others(6): Show |
intron_variant | MODIFIER | c.516+2446C>T | RRAGB | ENSG00000083750.13 | transcript | ENST00000374941.9 | protein_coding | 5/9 | chrX | 55734032 | |||||||
| chrX:55734125 | A | G | 140 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(137): Show |
225 | HG00140.hp1 HG00280.hp1 HG00423.hp1 others(222): Show |
intron_variant | MODIFIER | c.516+2539A>G | RRAGB | ENSG00000083750.13 | transcript | ENST00000374941.9 | protein_coding | 5/9 | chrX | 55734125 | |||||||
| chrX:55734206 | G | A | 1 | a0001c0001t0001g0086 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.516+2620G>A | RRAGB | ENSG00000083750.13 | transcript | ENST00000374941.9 | protein_coding | 5/9 | chrX | 55734206 | |||||||
| chrX:55734252 | C | T | 1 | a0001c0001t0001g0060 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.516+2666C>T | RRAGB | ENSG00000083750.13 | transcript | ENST00000374941.9 | protein_coding | 5/9 | chrX | 55734252 | |||||||
| chrX:55734265 | G | GT | 10 | a0001c0001t0001g0021 a0001c0001t0001g0025 a0001c0001t0001g0058 others(7): Show |
11 | HG00544.hp1 HG02572.hp1 HG02809.hp2 others(8): Show |
intron_variant | MODIFIER | c.516+2694dupT | RRAGB | ENSG00000083750.13 | transcript | ENST00000374941.9 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chrX | 55734265 | ||||||
| chrX:55734273 | T | G | 1 | a0001c0001t0001g0029 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.516+2687T>G | RRAGB | ENSG00000083750.13 | transcript | ENST00000374941.9 | protein_coding | 5/9 | chrX | 55734273 | |||||||
| chrX:55734344 | T | G | 1 | a0001c0001t0001g0032 | 1 | HG03492.hp1 | intron_variant | MODIFIER | c.516+2758T>G | RRAGB | ENSG00000083750.13 | transcript | ENST00000374941.9 | protein_coding | 5/9 | chrX | 55734344 | |||||||
| chrX:55734589 | T | C | 1 | a0001c0001t0001g0025 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.516+3003T>C | RRAGB | ENSG00000083750.13 | transcript | ENST00000374941.9 | protein_coding | 5/9 | chrX | 55734589 | |||||||
| chrX:55734778 | G | T | 1 | a0001c0001t0002g0156 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.516+3192G>T | RRAGB | ENSG00000083750.13 | transcript | ENST00000374941.9 | protein_coding | 5/9 | chrX | 55734778 | |||||||
| chrX:55734799 | A | G | 1 | a0001c0001t0001g0109 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.516+3213A>G | RRAGB | ENSG00000083750.13 | transcript | ENST00000374941.9 | protein_coding | 5/9 | chrX | 55734799 | |||||||
| chrX:55735141 | T | G | 140 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(137): Show |
225 | HG00140.hp1 HG00280.hp1 HG00423.hp1 others(222): Show |
intron_variant | MODIFIER | c.516+3555T>G | RRAGB | ENSG00000083750.13 | transcript | ENST00000374941.9 | protein_coding | 5/9 | chrX | 55735141 | |||||||
| chrX:55735500 | G | T | 1 | a0001c0001t0002g0153 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.516+3914G>T | RRAGB | ENSG00000083750.13 | transcript | ENST00000374941.9 | protein_coding | 5/9 | chrX | 55735500 | |||||||
| chrX:55735583 | T | C | 1 | a0001c0001t0002g0132 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.516+3997T>C | RRAGB | ENSG00000083750.13 | transcript | ENST00000374941.9 | protein_coding | 5/9 | chrX | 55735583 | |||||||
| chrX:55736332 | G | T | 1 | a0001c0001t0002g0118 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.516+4746G>T | RRAGB | ENSG00000083750.13 | transcript | ENST00000374941.9 | protein_coding | 5/9 | chrX | 55736332 | |||||||
| chrX:55736695 | G | A | 1 | a0001c0001t0002g0117 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.516+5109G>A | RRAGB | ENSG00000083750.13 | transcript | ENST00000374941.9 | protein_coding | 5/9 | chrX | 55736695 | |||||||
| chrX:55736890 | C | T | 71 | a0001c0001t0002g0002 a0001c0001t0002g0008 a0001c0001t0002g0012 others(68): Show |
99 | HG00140.hp1 HG00423.hp2 HG00544.hp1 others(96): Show |
intron_variant | MODIFIER | c.516+5304C>T | RRAGB | ENSG00000083750.13 | transcript | ENST00000374941.9 | protein_coding | 5/9 | chrX | 55736890 | |||||||
| chrX:55736977 | A | G | 2 | a0001c0001t0002g0113 a0001c0001t0002g0114 |
2 | HG01167.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.516+5391A>G | RRAGB | ENSG00000083750.13 | transcript | ENST00000374941.9 | protein_coding | 5/9 | chrX | 55736977 | |||||||
| chrX:55737215 | C | G | 8 | a0001c0001t0002g0008 a0001c0001t0002g0113 a0001c0001t0002g0114 others(5): Show |
12 | HG00738.hp1 HG01167.hp1 HG01169.hp1 others(9): Show |
intron_variant | MODIFIER | c.516+5629C>G | RRAGB | ENSG00000083750.13 | transcript | ENST00000374941.9 | protein_coding | 5/9 | chrX | 55737215 | |||||||
| chrX:55737652 | C | T | 1 | a0001c0001t0001g0025 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.516+6066C>T | RRAGB | ENSG00000083750.13 | transcript | ENST00000374941.9 | protein_coding | 5/9 | chrX | 55737652 | |||||||
| chrX:55737665 | G | A | 1 | a0001c0001t0002g0153 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.516+6079G>A | RRAGB | ENSG00000083750.13 | transcript | ENST00000374941.9 | protein_coding | 5/9 | chrX | 55737665 | |||||||
| chrX:55737913 | G | A | 8 | a0001c0001t0002g0008 a0001c0001t0002g0113 a0001c0001t0002g0114 others(5): Show |
12 | HG00738.hp1 HG01167.hp1 HG01169.hp1 others(9): Show |
intron_variant | MODIFIER | c.516+6327G>A | RRAGB | ENSG00000083750.13 | transcript | ENST00000374941.9 | protein_coding | 5/9 | chrX | 55737913 | |||||||
| chrX:55737937 | G | A | 2 | a0001c0001t0001g0104 a0001c0001t0001g0105 |
2 | HG02257.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.516+6351G>A | RRAGB | ENSG00000083750.13 | transcript | ENST00000374941.9 | protein_coding | 5/9 | chrX | 55737937 | |||||||
| chrX:55738041 | G | A | 1 | a0001c0001t0001g0104 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.516+6455G>A | RRAGB | ENSG00000083750.13 | transcript | ENST00000374941.9 | protein_coding | 5/9 | chrX | 55738041 | |||||||
| chrX:55738191 | C | T | 1 | a0001c0001t0002g0166 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.516+6605C>T | RRAGB | ENSG00000083750.13 | transcript | ENST00000374941.9 | protein_coding | 5/9 | chrX | 55738191 | |||||||
| chrX:55738268 | GCTT | G | 8 | a0001c0001t0002g0008 a0001c0001t0002g0113 a0001c0001t0002g0114 others(5): Show |
12 | HG00738.hp1 HG01167.hp1 HG01169.hp1 others(9): Show |
intron_variant | MODIFIER | c.516+6686_516+6688d others(5): Show |
RRAGB | ENSG00000083750.13 | transcript | ENST00000374941.9 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chrX | 55738268 | ||||||
| chrX:55738380 | A | G | 140 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(137): Show |
225 | HG00140.hp1 HG00280.hp1 HG00423.hp1 others(222): Show |
intron_variant | MODIFIER | c.516+6794A>G | RRAGB | ENSG00000083750.13 | transcript | ENST00000374941.9 | protein_coding | 5/9 | chrX | 55738380 | |||||||
| chrX:55738546 | A | G | 1 | a0001c0001t0002g0132 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.516+6960A>G | RRAGB | ENSG00000083750.13 | transcript | ENST00000374941.9 | protein_coding | 5/9 | chrX | 55738546 | |||||||
| chrX:55738870 | G | A | 1 | a0001c0001t0002g0133 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.516+7284G>A | RRAGB | ENSG00000083750.13 | transcript | ENST00000374941.9 | protein_coding | 5/9 | chrX | 55738870 | |||||||
| chrX:55739402 | CT | C | 140 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(137): Show |
225 | HG00140.hp1 HG00280.hp1 HG00423.hp1 others(222): Show |
intron_variant | MODIFIER | c.516+7818delT | RRAGB | ENSG00000083750.13 | transcript | ENST00000374941.9 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chrX | 55739402 | ||||||
| chrX:55739591 | T | C | 1 | a0001c0001t0002g0134 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.516+8005T>C | RRAGB | ENSG00000083750.13 | transcript | ENST00000374941.9 | protein_coding | 5/9 | chrX | 55739591 | |||||||
| chrX:55739600 | C | T | 73 | a0001c0001t0002g0002 a0001c0001t0002g0008 a0001c0001t0002g0012 others(70): Show |
102 | HG00140.hp1 HG00423.hp2 HG00544.hp1 others(99): Show |
intron_variant | MODIFIER | c.516+8014C>T | RRAGB | ENSG00000083750.13 | transcript | ENST00000374941.9 | protein_coding | 5/9 | chrX | 55739600 | |||||||
| chrX:55739864 | G | A | 67 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(64): Show |
123 | HG00280.hp1 HG00423.hp1 HG00544.hp2 others(120): Show |
intron_variant | MODIFIER | c.516+8278G>A | RRAGB | ENSG00000083750.13 | transcript | ENST00000374941.9 | protein_coding | 5/9 | chrX | 55739864 | |||||||
| chrX:55740094 | G | A | 1 | a0001c0001t0001g0025 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.516+8508G>A | RRAGB | ENSG00000083750.13 | transcript | ENST00000374941.9 | protein_coding | 5/9 | chrX | 55740094 | |||||||
| chrX:55740119 | G | A | 1 | a0001c0001t0001g0020 | 2 | HG02109.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.516+8533G>A | RRAGB | ENSG00000083750.13 | transcript | ENST00000374941.9 | protein_coding | 5/9 | chrX | 55740119 | |||||||
| chrX:55740184 | G | A | 1 | a0001c0001t0001g0091 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.516+8598G>A | RRAGB | ENSG00000083750.13 | transcript | ENST00000374941.9 | protein_coding | 5/9 | chrX | 55740184 | |||||||
| chrX:55740304 | A | C | 1 | a0001c0001t0001g0025 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.516+8718A>C | RRAGB | ENSG00000083750.13 | transcript | ENST00000374941.9 | protein_coding | 5/9 | chrX | 55740304 | |||||||
| chrX:55740310 | A | G | 1 | a0001c0001t0001g0025 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.516+8724A>G | RRAGB | ENSG00000083750.13 | transcript | ENST00000374941.9 | protein_coding | 5/9 | chrX | 55740310 | |||||||
| chrX:55740318 | A | G | 1 | a0001c0001t0001g0025 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.516+8732A>G | RRAGB | ENSG00000083750.13 | transcript | ENST00000374941.9 | protein_coding | 5/9 | chrX | 55740318 | |||||||
| chrX:55740322 | C | CA | 4 | a0001c0001t0001g0009 a0001c0001t0001g0060 a0001c0001t0002g0135 others(1): Show |
7 | HG03490.hp1 HG03831.hp1 HG03834.hp2 others(4): Show |
intron_variant | MODIFIER | c.516+8749dupA | RRAGB | ENSG00000083750.13 | transcript | ENST00000374941.9 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chrX | 55740322 | ||||||
| chrX:55740336 | T | A | 1 | a0001c0001t0001g0025 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.516+8750T>A | RRAGB | ENSG00000083750.13 | transcript | ENST00000374941.9 | protein_coding | 5/9 | chrX | 55740336 | |||||||
| chrX:55740337 | C | A | 1 | a0001c0001t0001g0025 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.516+8751C>A | RRAGB | ENSG00000083750.13 | transcript | ENST00000374941.9 | protein_coding | 5/9 | chrX | 55740337 | |||||||
| chrX:55740338 | ATTGTGAT others(37): Show |
A | 1 | a0001c0001t0001g0025 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.516+8753_516+8796d others(46): Show |
RRAGB | ENSG00000083750.13 | transcript | ENST00000374941.9 | protein_coding | 5/9 | chrX | 55740338 | |||||||
| chrX:55740386 | C | A | 1 | a0001c0001t0001g0025 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.516+8800C>A | RRAGB | ENSG00000083750.13 | transcript | ENST00000374941.9 | protein_coding | 5/9 | chrX | 55740386 | |||||||
| chrX:55740388 | C | A | 1 | a0001c0001t0001g0025 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.516+8802C>A | RRAGB | ENSG00000083750.13 | transcript | ENST00000374941.9 | protein_coding | 5/9 | chrX | 55740388 | |||||||
| chrX:55740396 | G | A | 1 | a0001c0001t0001g0025 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.516+8810G>A | RRAGB | ENSG00000083750.13 | transcript | ENST00000374941.9 | protein_coding | 5/9 | chrX | 55740396 | |||||||
| chrX:55740397 | G | A | 1 | a0001c0001t0001g0025 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.516+8811G>A | RRAGB | ENSG00000083750.13 | transcript | ENST00000374941.9 | protein_coding | 5/9 | chrX | 55740397 | |||||||
| chrX:55740400 | T | A | 1 | a0001c0001t0001g0025 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.516+8814T>A | RRAGB | ENSG00000083750.13 | transcript | ENST00000374941.9 | protein_coding | 5/9 | chrX | 55740400 | |||||||
| chrX:55740478 | G | A | 1 | a0001c0001t0001g0025 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.516+8892G>A | RRAGB | ENSG00000083750.13 | transcript | ENST00000374941.9 | protein_coding | 5/9 | chrX | 55740478 | |||||||
| chrX:55740531 | G | A | 1 | a0001c0001t0001g0025 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.516+8945G>A | RRAGB | ENSG00000083750.13 | transcript | ENST00000374941.9 | protein_coding | 5/9 | chrX | 55740531 | |||||||
| chrX:55741014 | A | G | 1 | a0001c0001t0002g0118 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.516+9428A>G | RRAGB | ENSG00000083750.13 | transcript | ENST00000374941.9 | protein_coding | 5/9 | chrX | 55741014 | |||||||
| chrX:55741025 | A | AT | 5 | a0001c0001t0001g0101 a0001c0001t0002g0116 a0001c0001t0002g0150 others(2): Show |
5 | HG01175.hp1 HG02071.hp1 HG02818.hp2 others(2): Show |
intron_variant | MODIFIER | c.516+9457dupT | RRAGB | ENSG00000083750.13 | transcript | ENST00000374941.9 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chrX | 55741025 | ||||||
| chrX:55741025 | AT | A | 8 | a0001c0001t0001g0025 a0001c0001t0001g0056 a0001c0001t0001g0057 others(5): Show |
8 | HG03516.hp2 HG03688.hp1 NA18966.hp1 others(5): Show |
intron_variant | MODIFIER | c.516+9457delT | RRAGB | ENSG00000083750.13 | transcript | ENST00000374941.9 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chrX | 55741025 | ||||||
| chrX:55741025 | ATT | A | 61 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(58): Show |
117 | HG00280.hp1 HG00423.hp1 HG00544.hp2 others(114): Show |
intron_variant | MODIFIER | c.516+9456_516+9457d others(4): Show |
RRAGB | ENSG00000083750.13 | transcript | ENST00000374941.9 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chrX | 55741025 | ||||||
| chrX:55741125 | G | A | 4 | a0001c0001t0001g0033 a0001c0001t0001g0034 a0001c0001t0001g0035 others(1): Show |
4 | HG00735.hp2 HG01081.hp2 HG01256.hp1 others(1): Show |
intron_variant | MODIFIER | c.516+9539G>A | RRAGB | ENSG00000083750.13 | transcript | ENST00000374941.9 | protein_coding | 5/9 | chrX | 55741125 | |||||||
| chrX:55741290 | G | A | 3 | a0001c0001t0001g0090 a0001c0001t0001g0106 a0001c0001t0001g0107 |
3 | HG01255.hp1 HG02630.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.516+9704G>A | RRAGB | ENSG00000083750.13 | transcript | ENST00000374941.9 | protein_coding | 5/9 | chrX | 55741290 | |||||||
| chrX:55741483 | A | C | 2 | a0001c0001t0001g0086 a0001c0001t0001g0103 |
2 | HG02451.hp1 HG02615.hp2 |
intron_variant | MODIFIER | c.517-9618A>C | RRAGB | ENSG00000083750.13 | transcript | ENST00000374941.9 | protein_coding | 5/9 | chrX | 55741483 | |||||||
| chrX:55742059 | C | T | 1 | a0001c0001t0002g0152 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.517-9042C>T | RRAGB | ENSG00000083750.13 | transcript | ENST00000374941.9 | protein_coding | 5/9 | chrX | 55742059 | |||||||
| chrX:55742112 | T | C | 1 | a0001c0001t0002g0172 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.517-8989T>C | RRAGB | ENSG00000083750.13 | transcript | ENST00000374941.9 | protein_coding | 5/9 | chrX | 55742112 | |||||||
| chrX:55742205 | A | G | 1 | a0001c0001t0001g0075 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.517-8896A>G | RRAGB | ENSG00000083750.13 | transcript | ENST00000374941.9 | protein_coding | 5/9 | chrX | 55742205 | |||||||
| chrX:55742275 | A | G | 1 | a0001c0001t0002g0135 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.517-8826A>G | RRAGB | ENSG00000083750.13 | transcript | ENST00000374941.9 | protein_coding | 5/9 | chrX | 55742275 | |||||||
| chrX:55742513 | C | G | 1 | a0001c0001t0002g0149 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.517-8588C>G | RRAGB | ENSG00000083750.13 | transcript | ENST00000374941.9 | protein_coding | 5/9 | chrX | 55742513 | |||||||
| chrX:55742979 | G | A | 1 | a0001c0001t0002g0136 | 1 | NA18939.hp1 | intron_variant | MODIFIER | c.517-8122G>A | RRAGB | ENSG00000083750.13 | transcript | ENST00000374941.9 | protein_coding | 5/9 | chrX | 55742979 | |||||||
| chrX:55743166 | G | A | 1 | a0001c0001t0001g0020 | 2 | HG02109.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.517-7935G>A | RRAGB | ENSG00000083750.13 | transcript | ENST00000374941.9 | protein_coding | 5/9 | chrX | 55743166 | |||||||
| chrX:55743313 | T | C | 1 | a0001c0001t0001g0036 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.517-7788T>C | RRAGB | ENSG00000083750.13 | transcript | ENST00000374941.9 | protein_coding | 5/9 | chrX | 55743313 | |||||||
| chrX:55743677 | A | G | 1 | a0001c0001t0002g0149 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.517-7424A>G | RRAGB | ENSG00000083750.13 | transcript | ENST00000374941.9 | protein_coding | 5/9 | chrX | 55743677 | |||||||
| chrX:55743814 | A | G | 146 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(143): Show |
231 | HG00140.hp1 HG00280.hp1 HG00423.hp1 others(228): Show |
intron_variant | MODIFIER | c.517-7287A>G | RRAGB | ENSG00000083750.13 | transcript | ENST00000374941.9 | protein_coding | 5/9 | chrX | 55743814 | |||||||
| chrX:55743911 | A | AACTTTCT others(19): Show |
1 | a0001c0001t0002g0167 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.517-7181_517-7156d others(28): Show |
RRAGB | ENSG00000083750.13 | transcript | ENST00000374941.9 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chrX | 55743911 | ||||||
| chrX:55743921 | C | T | 1 | a0001c0001t0001g0055 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.517-7180C>T | RRAGB | ENSG00000083750.13 | transcript | ENST00000374941.9 | protein_coding | 5/9 | chrX | 55743921 | |||||||
| chrX:55744088 | A | G | 140 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(137): Show |
225 | HG00140.hp1 HG00280.hp1 HG00423.hp1 others(222): Show |
intron_variant | MODIFIER | c.517-7013A>G | RRAGB | ENSG00000083750.13 | transcript | ENST00000374941.9 | protein_coding | 5/9 | chrX | 55744088 | |||||||
| chrX:55744321 | G | A | 1 | a0001c0001t0002g0129 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.517-6780G>A | RRAGB | ENSG00000083750.13 | transcript | ENST00000374941.9 | protein_coding | 5/9 | chrX | 55744321 | |||||||
| chrX:55744387 | C | CAAAAAAA others(5): Show |
7 | a0001c0001t0001g0053 a0001c0001t0001g0054 a0001c0001t0001g0074 others(4): Show |
7 | HG02647.hp1 NA18939.hp2 NA18946.hp1 others(4): Show |
intron_variant | MODIFIER | c.517-6708_517-6697d others(14): Show |
RRAGB | ENSG00000083750.13 | transcript | ENST00000374941.9 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chrX | 55744387 | ||||||
| chrX:55744387 | C | CAAAAAAA others(6): Show |
88 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0007 others(85): Show |
159 | HG00140.hp1 HG00280.hp1 HG00423.hp2 others(156): Show |
intron_variant | MODIFIER | c.517-6709_517-6697d others(15): Show |
RRAGB | ENSG00000083750.13 | transcript | ENST00000374941.9 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chrX | 55744387 | ||||||
| chrX:55744387 | C | CAAAAAAA others(7): Show |
34 | a0001c0001t0001g0003 a0001c0001t0001g0016 a0001c0001t0001g0029 others(31): Show |
48 | HG00423.hp1 HG00544.hp1 HG00609.hp1 others(45): Show |
intron_variant | MODIFIER | c.517-6710_517-6697d others(16): Show |
RRAGB | ENSG00000083750.13 | transcript | ENST00000374941.9 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chrX | 55744387 | ||||||
| chrX:55744387 | C | CAAAAAAA others(8): Show |
3 | a0001c0001t0002g0115 a0001c0001t0002g0127 a0001c0001t0002g0171 |
3 | HG02258.hp1 HG02559.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.517-6711_517-6697d others(17): Show |
RRAGB | ENSG00000083750.13 | transcript | ENST00000374941.9 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chrX | 55744387 | ||||||
| chrX:55744387 | C | CAAAAAAA others(9): Show |
1 | a0001c0001t0002g0169 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.517-6712_517-6697d others(18): Show |
RRAGB | ENSG00000083750.13 | transcript | ENST00000374941.9 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chrX | 55744387 | ||||||
| chrX:55744387 | C | CAAAAAAA others(13): Show |
1 | a0001c0001t0002g0119 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.517-6697_517-6696i others(22): Show |
RRAGB | ENSG00000083750.13 | transcript | ENST00000374941.9 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chrX | 55744387 | ||||||
| chrX:55744387 | C | CAAAAAAA others(16): Show |
1 | a0001c0001t0002g0167 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.517-6697_517-6696i others(25): Show |
RRAGB | ENSG00000083750.13 | transcript | ENST00000374941.9 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chrX | 55744387 | ||||||
| chrX:55744387 | C | CAAAAAAA others(17): Show |
1 | a0001c0001t0002g0170 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.517-6697_517-6696i others(26): Show |
RRAGB | ENSG00000083750.13 | transcript | ENST00000374941.9 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chrX | 55744387 | ||||||
| chrX:55744387 | C | CAAAAAAA others(18): Show |
1 | a0001c0001t0002g0168 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.517-6697_517-6696i others(27): Show |
RRAGB | ENSG00000083750.13 | transcript | ENST00000374941.9 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chrX | 55744387 | ||||||
| chrX:55744387 | C | CAAAAAAA others(29): Show |
2 | a0001c0001t0002g0113 a0001c0001t0002g0114 |
2 | HG01167.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.517-6697_517-6696i others(38): Show |
RRAGB | ENSG00000083750.13 | transcript | ENST00000374941.9 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chrX | 55744387 | ||||||
| chrX:55744408 | G | C | 67 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(64): Show |
123 | HG00280.hp1 HG00423.hp1 HG00544.hp2 others(120): Show |
intron_variant | MODIFIER | c.517-6693G>C | RRAGB | ENSG00000083750.13 | transcript | ENST00000374941.9 | protein_coding | 5/9 | chrX | 55744408 | |||||||
| chrX:55744701 | A | G | 2 | a0001c0001t0001g0099 a0001c0001t0001g0104 |
2 | HG00735.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.517-6400A>G | RRAGB | ENSG00000083750.13 | transcript | ENST00000374941.9 | protein_coding | 5/9 | chrX | 55744701 | |||||||
| chrX:55744902 | A | G | 2 | a0001c0001t0002g0113 a0001c0001t0002g0114 |
2 | HG01167.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.517-6199A>G | RRAGB | ENSG00000083750.13 | transcript | ENST00000374941.9 | protein_coding | 5/9 | chrX | 55744902 | |||||||
| chrX:55745056 | C | T | 1 | a0001c0001t0001g0105 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.517-6045C>T | RRAGB | ENSG00000083750.13 | transcript | ENST00000374941.9 | protein_coding | 5/9 | chrX | 55745056 | |||||||
| chrX:55745285 | T | C | 2 | a0001c0001t0001g0100 a0001c0001t0001g0101 |
2 | HG00642.hp1 HG01175.hp1 |
intron_variant | MODIFIER | c.517-5816T>C | RRAGB | ENSG00000083750.13 | transcript | ENST00000374941.9 | protein_coding | 5/9 | chrX | 55745285 | |||||||
| chrX:55745352 | A | G | 1 | a0001c0001t0002g0138 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.517-5749A>G | RRAGB | ENSG00000083750.13 | transcript | ENST00000374941.9 | protein_coding | 5/9 | chrX | 55745352 | |||||||
| chrX:55745577 | T | C | 1 | a0001c0001t0002g0139 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.517-5524T>C | RRAGB | ENSG00000083750.13 | transcript | ENST00000374941.9 | protein_coding | 5/9 | chrX | 55745577 | |||||||
| chrX:55745767 | A | G | 6 | a0001c0001t0001g0090 a0001c0001t0001g0099 a0001c0001t0001g0104 others(3): Show |
6 | HG00735.hp1 HG01255.hp1 HG02257.hp2 others(3): Show |
intron_variant | MODIFIER | c.517-5334A>G | RRAGB | ENSG00000083750.13 | transcript | ENST00000374941.9 | protein_coding | 5/9 | chrX | 55745767 | |||||||
| chrX:55745959 | A | C | 172 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(169): Show |
271 | HG00140.hp1 HG00280.hp1 HG00423.hp1 others(268): Show |
intron_variant | MODIFIER | c.517-5142A>C | RRAGB | ENSG00000083750.13 | transcript | ENST00000374941.9 | protein_coding | 5/9 | chrX | 55745959 | |||||||
| chrX:55746221 | T | C | 73 | a0001c0001t0002g0002 a0001c0001t0002g0008 a0001c0001t0002g0012 others(70): Show |
102 | HG00140.hp1 HG00423.hp2 HG00544.hp1 others(99): Show |
intron_variant | MODIFIER | c.517-4880T>C | RRAGB | ENSG00000083750.13 | transcript | ENST00000374941.9 | protein_coding | 5/9 | chrX | 55746221 | |||||||
| chrX:55746620 | C | T | 1 | a0001c0001t0002g0164 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.517-4481C>T | RRAGB | ENSG00000083750.13 | transcript | ENST00000374941.9 | protein_coding | 5/9 | chrX | 55746620 | |||||||
| chrX:55746657 | A | G | 1 | a0001c0001t0001g0112 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.517-4444A>G | RRAGB | ENSG00000083750.13 | transcript | ENST00000374941.9 | protein_coding | 5/9 | chrX | 55746657 | |||||||
| chrX:55746752 | G | A | 2 | a0001c0001t0002g0113 a0001c0001t0002g0114 |
2 | HG01167.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.517-4349G>A | RRAGB | ENSG00000083750.13 | transcript | ENST00000374941.9 | protein_coding | 5/9 | chrX | 55746752 | |||||||
| chrX:55746982 | G | A | 1 | a0001c0001t0001g0030 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.517-4119G>A | RRAGB | ENSG00000083750.13 | transcript | ENST00000374941.9 | protein_coding | 5/9 | chrX | 55746982 | |||||||
| chrX:55747198 | T | G | 1 | a0001c0001t0001g0025 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.517-3903T>G | RRAGB | ENSG00000083750.13 | transcript | ENST00000374941.9 | protein_coding | 5/9 | chrX | 55747198 | |||||||
| chrX:55747213 | G | A | 66 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(63): Show |
122 | HG00280.hp1 HG00423.hp1 HG00544.hp2 others(119): Show |
intron_variant | MODIFIER | c.517-3888G>A | RRAGB | ENSG00000083750.13 | transcript | ENST00000374941.9 | protein_coding | 5/9 | chrX | 55747213 | |||||||
| chrX:55747293 | A | T | 1 | a0001c0001t0001g0112 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.517-3808A>T | RRAGB | ENSG00000083750.13 | transcript | ENST00000374941.9 | protein_coding | 5/9 | chrX | 55747293 | |||||||
| chrX:55747592 | G | A | 2 | a0001c0001t0002g0113 a0001c0001t0002g0114 |
2 | HG01167.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.517-3509G>A | RRAGB | ENSG00000083750.13 | transcript | ENST00000374941.9 | protein_coding | 5/9 | chrX | 55747592 | |||||||
| chrX:55747654 | G | T | 68 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(65): Show |
125 | HG00280.hp1 HG00423.hp1 HG00544.hp2 others(122): Show |
intron_variant | MODIFIER | c.517-3447G>T | RRAGB | ENSG00000083750.13 | transcript | ENST00000374941.9 | protein_coding | 5/9 | chrX | 55747654 | |||||||
| chrX:55747707 | C | G | 1 | a0001c0001t0001g0025 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.517-3394C>G | RRAGB | ENSG00000083750.13 | transcript | ENST00000374941.9 | protein_coding | 5/9 | chrX | 55747707 | |||||||
| chrX:55747812 | G | GCTCCCT | 16 | a0001c0001t0001g0016 a0001c0001t0001g0032 a0001c0001t0001g0041 others(13): Show |
21 | HG00735.hp1 HG00738.hp1 HG02083.hp1 others(18): Show |
intron_variant | MODIFIER | c.517-3259_517-3254d others(8): Show |
RRAGB | ENSG00000083750.13 | transcript | ENST00000374941.9 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chrX | 55747812 | ||||||
| chrX:55747812 | G | GCTCCCTC others(5): Show |
59 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(56): Show |
115 | HG00423.hp1 HG00544.hp2 HG00673.hp1 others(112): Show |
intron_variant | MODIFIER | c.517-3265_517-3254d others(14): Show |
RRAGB | ENSG00000083750.13 | transcript | ENST00000374941.9 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chrX | 55747812 | ||||||
| chrX:55747812 | G | GCTCCCTC others(11): Show |
5 | a0001c0001t0001g0039 a0001c0001t0001g0052 a0001c0001t0001g0074 others(2): Show |
5 | HG00609.hp1 HG01255.hp1 HG01884.hp2 others(2): Show |
intron_variant | MODIFIER | c.517-3271_517-3254d others(20): Show |
RRAGB | ENSG00000083750.13 | transcript | ENST00000374941.9 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chrX | 55747812 | ||||||
| chrX:55747812 | GCTCCCTC others(5): Show |
G | 63 | a0001c0001t0002g0002 a0001c0001t0002g0012 a0001c0001t0002g0013 others(60): Show |
87 | HG00140.hp1 HG00423.hp2 HG00544.hp1 others(84): Show |
intron_variant | MODIFIER | c.517-3265_517-3254d others(14): Show |
RRAGB | ENSG00000083750.13 | transcript | ENST00000374941.9 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chrX | 55747812 | ||||||
| chrX:55747836 | TCTCCCTC others(5): Show |
T | 3 | a0001c0001t0001g0093 a0001c0001t0001g0100 a0001c0001t0001g0101 |
3 | HG00642.hp1 HG00733.hp2 HG01175.hp1 |
intron_variant | MODIFIER | c.517-3264_517-3253d others(14): Show |
RRAGB | ENSG00000083750.13 | transcript | ENST00000374941.9 | protein_coding | 5/9 | chrX | 55747836 | |||||||
| chrX:55747967 | G | T | 6 | a0001c0001t0001g0067 a0001c0001t0001g0071 a0001c0001t0001g0072 others(3): Show |
7 | HG01257.hp1 HG01258.hp1 HG01496.hp2 others(4): Show |
intron_variant | MODIFIER | c.517-3134G>T | RRAGB | ENSG00000083750.13 | transcript | ENST00000374941.9 | protein_coding | 5/9 | chrX | 55747967 | |||||||
| chrX:55748066 | C | T | 71 | a0001c0001t0002g0002 a0001c0001t0002g0008 a0001c0001t0002g0012 others(68): Show |
99 | HG00140.hp1 HG00423.hp2 HG00544.hp1 others(96): Show |
intron_variant | MODIFIER | c.517-3035C>T | RRAGB | ENSG00000083750.13 | transcript | ENST00000374941.9 | protein_coding | 5/9 | chrX | 55748066 | |||||||
| chrX:55748112 | C | T | 1 | a0001c0001t0002g0147 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.517-2989C>T | RRAGB | ENSG00000083750.13 | transcript | ENST00000374941.9 | protein_coding | 5/9 | chrX | 55748112 | |||||||
| chrX:55748137 | C | G | 1 | a0001c0001t0001g0092 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.517-2964C>G | RRAGB | ENSG00000083750.13 | transcript | ENST00000374941.9 | protein_coding | 5/9 | chrX | 55748137 | |||||||
| chrX:55748138 | G | A | 1 | a0001c0001t0001g0092 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.517-2963G>A | RRAGB | ENSG00000083750.13 | transcript | ENST00000374941.9 | protein_coding | 5/9 | chrX | 55748138 | |||||||
| chrX:55748179 | G | A | 1 | a0001c0001t0002g0121 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.517-2922G>A | RRAGB | ENSG00000083750.13 | transcript | ENST00000374941.9 | protein_coding | 5/9 | chrX | 55748179 | |||||||
| chrX:55748236 | T | C | 140 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(137): Show |
225 | HG00140.hp1 HG00280.hp1 HG00423.hp1 others(222): Show |
intron_variant | MODIFIER | c.517-2865T>C | RRAGB | ENSG00000083750.13 | transcript | ENST00000374941.9 | protein_coding | 5/9 | chrX | 55748236 | |||||||
| chrX:55748311 | G | A | 1 | a0001c0001t0002g0172 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.517-2790G>A | RRAGB | ENSG00000083750.13 | transcript | ENST00000374941.9 | protein_coding | 5/9 | chrX | 55748311 | |||||||
| chrX:55748347 | A | G | 69 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(66): Show |
126 | HG00280.hp1 HG00423.hp1 HG00544.hp2 others(123): Show |
intron_variant | MODIFIER | c.517-2754A>G | RRAGB | ENSG00000083750.13 | transcript | ENST00000374941.9 | protein_coding | 5/9 | chrX | 55748347 | |||||||
| chrX:55748441 | G | A | 71 | a0001c0001t0002g0002 a0001c0001t0002g0008 a0001c0001t0002g0012 others(68): Show |
99 | HG00140.hp1 HG00423.hp2 HG00544.hp1 others(96): Show |
intron_variant | MODIFIER | c.517-2660G>A | RRAGB | ENSG00000083750.13 | transcript | ENST00000374941.9 | protein_coding | 5/9 | chrX | 55748441 | |||||||
| chrX:55748480 | C | T | 68 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(65): Show |
125 | HG00280.hp1 HG00423.hp1 HG00544.hp2 others(122): Show |
intron_variant | MODIFIER | c.517-2621C>T | RRAGB | ENSG00000083750.13 | transcript | ENST00000374941.9 | protein_coding | 5/9 | chrX | 55748480 | |||||||
| chrX:55748528 | T | A | 2 | a0001c0001t0002g0147 a0001c0001t0002g0153 |
2 | NA18956.hp1 NA18969.hp2 |
intron_variant | MODIFIER | c.517-2573T>A | RRAGB | ENSG00000083750.13 | transcript | ENST00000374941.9 | protein_coding | 5/9 | chrX | 55748528 | |||||||
| chrX:55748542 | C | T | 1 | a0001c0001t0001g0025 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.517-2559C>T | RRAGB | ENSG00000083750.13 | transcript | ENST00000374941.9 | protein_coding | 5/9 | chrX | 55748542 | |||||||
| chrX:55748564 | C | T | 1 | a0001c0001t0001g0078 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.517-2537C>T | RRAGB | ENSG00000083750.13 | transcript | ENST00000374941.9 | protein_coding | 5/9 | chrX | 55748564 | |||||||
| chrX:55748625 | C | T | 1 | a0001c0001t0002g0146 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.517-2476C>T | RRAGB | ENSG00000083750.13 | transcript | ENST00000374941.9 | protein_coding | 5/9 | chrX | 55748625 | |||||||
| chrX:55748636 | C | A | 1 | a0001c0001t0001g0068 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.517-2465C>A | RRAGB | ENSG00000083750.13 | transcript | ENST00000374941.9 | protein_coding | 5/9 | chrX | 55748636 | |||||||
| chrX:55748641 | C | T | 3 | a0001c0001t0002g0008 a0001c0001t0002g0115 a0001c0001t0002g0116 |
7 | HG02818.hp2 HG02886.hp1 HG02922.hp2 others(4): Show |
intron_variant | MODIFIER | c.517-2460C>T | RRAGB | ENSG00000083750.13 | transcript | ENST00000374941.9 | protein_coding | 5/9 | chrX | 55748641 | |||||||
| chrX:55748707 | G | A | 2 | a0001c0001t0001g0036 a0001c0001t0001g0043 |
2 | HG02135.hp1 NA18747.hp1 |
intron_variant | MODIFIER | c.517-2394G>A | RRAGB | ENSG00000083750.13 | transcript | ENST00000374941.9 | protein_coding | 5/9 | chrX | 55748707 | |||||||
| chrX:55748711 | G | A | 1 | a0001c0001t0002g0172 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.517-2390G>A | RRAGB | ENSG00000083750.13 | transcript | ENST00000374941.9 | protein_coding | 5/9 | chrX | 55748711 | |||||||
| chrX:55748855 | C | A | 2 | a0001c0001t0002g0113 a0001c0001t0002g0114 |
2 | HG01167.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.517-2246C>A | RRAGB | ENSG00000083750.13 | transcript | ENST00000374941.9 | protein_coding | 5/9 | chrX | 55748855 | |||||||
| chrX:55748878 | TGCCCGGC others(42): Show |
T | 1 | a0001c0001t0002g0023 | 2 | HG01168.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.517-2211_517-2163d others(51): Show |
RRAGB | ENSG00000083750.13 | transcript | ENST00000374941.9 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chrX | 55748878 | ||||||
| chrX:55748889 | C | G | 1 | a0001c0001t0001g0049 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.517-2212C>G | RRAGB | ENSG00000083750.13 | transcript | ENST00000374941.9 | protein_coding | 5/9 | chrX | 55748889 | |||||||
| chrX:55748890 | C | T | 1 | a0001c0001t0001g0031 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.517-2211C>T | RRAGB | ENSG00000083750.13 | transcript | ENST00000374941.9 | protein_coding | 5/9 | chrX | 55748890 | |||||||
| chrX:55748891 | G | A | 1 | a0001c0001t0001g0108 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.517-2210G>A | RRAGB | ENSG00000083750.13 | transcript | ENST00000374941.9 | protein_coding | 5/9 | chrX | 55748891 | |||||||
| chrX:55748896 | ATCCGGGA others(42): Show |
A | 1 | a0001c0001t0002g0145 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.517-2185_517-2137d others(51): Show |
RRAGB | ENSG00000083750.13 | transcript | ENST00000374941.9 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chrX | 55748896 | ||||||
| chrX:55748916 | GGTCAGCC others(42): Show |
G | 1 | a0001c0001t0001g0052 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.517-2173_517-2125d others(51): Show |
RRAGB | ENSG00000083750.13 | transcript | ENST00000374941.9 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chrX | 55748916 | ||||||
| chrX:55748970 | G | GC | 67 | a0001c0001t0001g0026 a0001c0001t0001g0044 a0001c0001t0001g0053 others(64): Show |
91 | HG00140.hp1 HG00423.hp2 HG00544.hp1 others(88): Show |
intron_variant | MODIFIER | c.517-2124dupC | RRAGB | ENSG00000083750.13 | transcript | ENST00000374941.9 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chrX | 55748970 | ||||||
| chrX:55748981 | C | T | 68 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(65): Show |
125 | HG00280.hp1 HG00423.hp1 HG00544.hp2 others(122): Show |
intron_variant | MODIFIER | c.517-2120C>T | RRAGB | ENSG00000083750.13 | transcript | ENST00000374941.9 | protein_coding | 5/9 | chrX | 55748981 | |||||||
| chrX:55748998 | C | T | 1 | a0001c0001t0001g0051 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.517-2103C>T | RRAGB | ENSG00000083750.13 | transcript | ENST00000374941.9 | protein_coding | 5/9 | chrX | 55748998 | |||||||
| chrX:55749062 | G | C | 3 | a0001c0001t0001g0099 a0001c0001t0001g0104 a0001c0001t0001g0105 |
3 | HG00735.hp1 HG02257.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.517-2039G>C | RRAGB | ENSG00000083750.13 | transcript | ENST00000374941.9 | protein_coding | 5/9 | chrX | 55749062 | |||||||
| chrX:55749070 | C | T | 66 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(63): Show |
123 | HG00280.hp1 HG00423.hp1 HG00544.hp2 others(120): Show |
intron_variant | MODIFIER | c.517-2031C>T | RRAGB | ENSG00000083750.13 | transcript | ENST00000374941.9 | protein_coding | 5/9 | chrX | 55749070 | |||||||
| chrX:55749076 | G | A | 5 | a0001c0001t0001g0021 a0001c0001t0001g0108 a0001c0001t0001g0110 others(2): Show |
6 | HG02572.hp1 HG02809.hp2 HG02970.hp2 others(3): Show |
intron_variant | MODIFIER | c.517-2025G>A | RRAGB | ENSG00000083750.13 | transcript | ENST00000374941.9 | protein_coding | 5/9 | chrX | 55749076 | |||||||
| chrX:55749183 | A | G | 146 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(143): Show |
231 | HG00140.hp1 HG00280.hp1 HG00423.hp1 others(228): Show |
intron_variant | MODIFIER | c.517-1918A>G | RRAGB | ENSG00000083750.13 | transcript | ENST00000374941.9 | protein_coding | 5/9 | chrX | 55749183 | |||||||
| chrX:55749288 | C | CCAGCCGC others(91): Show |
1 | a0001c0001t0002g0123 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.517-1723_517-1722i others(100): Show |
RRAGB | ENSG00000083750.13 | transcript | ENST00000374941.9 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chrX | 55749288 | ||||||
| chrX:55749302 | C | T | 1 | a0001c0001t0001g0097 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.517-1799C>T | RRAGB | ENSG00000083750.13 | transcript | ENST00000374941.9 | protein_coding | 5/9 | chrX | 55749302 | |||||||
| chrX:55749337 | CCAGCCGC others(41): Show |
C | 1 | a0001c0001t0002g0153 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.517-1753_517-1706d others(50): Show |
RRAGB | ENSG00000083750.13 | transcript | ENST00000374941.9 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chrX | 55749337 | ||||||
| chrX:55749449 | G | A | 1 | a0001c0001t0001g0025 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.517-1652G>A | RRAGB | ENSG00000083750.13 | transcript | ENST00000374941.9 | protein_coding | 5/9 | chrX | 55749449 | |||||||
| chrX:55749473 | G | A | 1 | a0001c0001t0001g0105 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.517-1628G>A | RRAGB | ENSG00000083750.13 | transcript | ENST00000374941.9 | protein_coding | 5/9 | chrX | 55749473 | |||||||
| chrX:55749490 | A | AGTGAGGA others(34): Show |
1 | a0001c0001t0001g0111 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.517-1587_517-1586i others(43): Show |
RRAGB | ENSG00000083750.13 | transcript | ENST00000374941.9 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chrX | 55749490 | ||||||
| chrX:55749511 | G | C | 1 | a0001c0001t0001g0030 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.517-1590G>C | RRAGB | ENSG00000083750.13 | transcript | ENST00000374941.9 | protein_coding | 5/9 | chrX | 55749511 | |||||||
| chrX:55749514 | A | G | 1 | a0001c0001t0001g0050 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.517-1587A>G | RRAGB | ENSG00000083750.13 | transcript | ENST00000374941.9 | protein_coding | 5/9 | chrX | 55749514 | |||||||
| chrX:55749635 | T | C | 69 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(66): Show |
126 | HG00280.hp1 HG00423.hp1 HG00544.hp2 others(123): Show |
intron_variant | MODIFIER | c.517-1466T>C | RRAGB | ENSG00000083750.13 | transcript | ENST00000374941.9 | protein_coding | 5/9 | chrX | 55749635 | |||||||
| chrX:55749788 | A | C | 69 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(66): Show |
126 | HG00280.hp1 HG00423.hp1 HG00544.hp2 others(123): Show |
intron_variant | MODIFIER | c.517-1313A>C | RRAGB | ENSG00000083750.13 | transcript | ENST00000374941.9 | protein_coding | 5/9 | chrX | 55749788 | |||||||
| chrX:55749884 | G | A | 1 | a0001c0001t0001g0055 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.517-1217G>A | RRAGB | ENSG00000083750.13 | transcript | ENST00000374941.9 | protein_coding | 5/9 | chrX | 55749884 | |||||||
| chrX:55749980 | T | C | 1 | a0001c0001t0001g0025 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.517-1121T>C | RRAGB | ENSG00000083750.13 | transcript | ENST00000374941.9 | protein_coding | 5/9 | chrX | 55749980 | |||||||
| chrX:55750048 | T | TA | 9 | a0001c0001t0001g0005 a0001c0001t0001g0031 a0001c0001t0001g0033 others(6): Show |
14 | HG01106.hp1 HG01255.hp1 HG02055.hp1 others(11): Show |
intron_variant | MODIFIER | c.517-1023dupA | RRAGB | ENSG00000083750.13 | transcript | ENST00000374941.9 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chrX | 55750048 | ||||||
| chrX:55750048 | TA | T | 66 | a0001c0001t0001g0010 a0001c0001t0001g0025 a0001c0001t0001g0028 others(63): Show |
91 | HG00140.hp1 HG00423.hp2 HG00544.hp1 others(88): Show |
intron_variant | MODIFIER | c.517-1023delA | RRAGB | ENSG00000083750.13 | transcript | ENST00000374941.9 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chrX | 55750048 | ||||||
| chrX:55750048 | TAA | T | 13 | a0001c0001t0002g0012 a0001c0001t0002g0013 a0001c0001t0002g0015 others(10): Show |
19 | HG00738.hp1 HG01081.hp1 HG01167.hp1 others(16): Show |
intron_variant | MODIFIER | c.517-1024_517-1023d others(4): Show |
RRAGB | ENSG00000083750.13 | transcript | ENST00000374941.9 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chrX | 55750048 | ||||||
| chrX:55750050 | A | T | 1 | a0001c0001t0001g0028 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.517-1051A>T | RRAGB | ENSG00000083750.13 | transcript | ENST00000374941.9 | protein_coding | 5/9 | chrX | 55750050 | |||||||
| chrX:55750184 | A | ATG | 5 | a0001c0001t0001g0019 a0001c0001t0001g0088 a0001c0001t0001g0098 others(2): Show |
6 | HG02055.hp1 HG02965.hp1 HG02976.hp1 others(3): Show |
intron_variant | MODIFIER | c.517-881_517-880dup others(2): Show |
RRAGB | ENSG00000083750.13 | transcript | ENST00000374941.9 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chrX | 55750184 | ||||||
| chrX:55750184 | ATG | A | 58 | a0001c0001t0001g0046 a0001c0001t0001g0051 a0001c0001t0001g0062 others(55): Show |
79 | HG00140.hp1 HG00544.hp1 HG01069.hp1 others(76): Show |
intron_variant | MODIFIER | c.517-881_517-880del others(2): Show |
RRAGB | ENSG00000083750.13 | transcript | ENST00000374941.9 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chrX | 55750184 | ||||||
| chrX:55750184 | ATGTG | A | 74 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(71): Show |
135 | HG00280.hp1 HG00423.hp1 HG00423.hp2 others(132): Show |
intron_variant | MODIFIER | c.517-883_517-880del others(4): Show |
RRAGB | ENSG00000083750.13 | transcript | ENST00000374941.9 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chrX | 55750184 | ||||||
| chrX:55750184 | ATGTGTGT others(7): Show |
A | 1 | a0001c0001t0002g0149 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.517-893_517-880del others(14): Show |
RRAGB | ENSG00000083750.13 | transcript | ENST00000374941.9 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chrX | 55750184 | ||||||
| chrX:55750307 | G | T | 3 | a0001c0001t0002g0143 a0001c0001t0002g0151 a0001c0001t0002g0154 |
3 | NA18964.hp2 NA18975.hp1 NA18983.hp1 |
intron_variant | MODIFIER | c.517-794G>T | RRAGB | ENSG00000083750.13 | transcript | ENST00000374941.9 | protein_coding | 5/9 | chrX | 55750307 | |||||||
| chrX:55750347 | A | G | 67 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(64): Show |
124 | HG00280.hp1 HG00423.hp1 HG00544.hp2 others(121): Show |
intron_variant | MODIFIER | c.517-754A>G | RRAGB | ENSG00000083750.13 | transcript | ENST00000374941.9 | protein_coding | 5/9 | chrX | 55750347 | |||||||
| chrX:55750369 | C | T | 1 | a0001c0001t0002g0148 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.517-732C>T | RRAGB | ENSG00000083750.13 | transcript | ENST00000374941.9 | protein_coding | 5/9 | chrX | 55750369 | |||||||
| chrX:55750907 | G | T | 1 | a0001c0001t0002g0146 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.517-194G>T | RRAGB | ENSG00000083750.13 | transcript | ENST00000374941.9 | protein_coding | 5/9 | chrX | 55750907 | |||||||
| chrX:55751209 | C | T | 1 | a0001c0001t0002g0142 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.612+13C>T | RRAGB | ENSG00000083750.13 | transcript | ENST00000374941.9 | protein_coding | 6/9 | chrX | 55751209 | |||||||
| chrX:55751248 | A | G | 2 | a0001c0001t0002g0165 a0001c0001t0002g0166 |
2 | HG02280.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.612+52A>G | RRAGB | ENSG00000083750.13 | transcript | ENST00000374941.9 | protein_coding | 6/9 | chrX | 55751248 | |||||||
| chrX:55751706 | T | C | 66 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(63): Show |
122 | HG00280.hp1 HG00423.hp1 HG00544.hp2 others(119): Show |
intron_variant | MODIFIER | c.612+510T>C | RRAGB | ENSG00000083750.13 | transcript | ENST00000374941.9 | protein_coding | 6/9 | chrX | 55751706 | |||||||
| chrX:55752094 | C | CT | 166 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(163): Show |
265 | HG00140.hp1 HG00280.hp1 HG00423.hp1 others(262): Show |
intron_variant | MODIFIER | c.612+911dupT | RRAGB | ENSG00000083750.13 | transcript | ENST00000374941.9 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chrX | 55752094 | ||||||
| chrX:55752799 | A | G | 2 | a0001c0001t0001g0099 a0001c0001t0001g0104 |
2 | HG00735.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.613-593A>G | RRAGB | ENSG00000083750.13 | transcript | ENST00000374941.9 | protein_coding | 6/9 | chrX | 55752799 | |||||||
| chrX:55753550 | T | C | 1 | a0001c0001t0001g0025 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.735+36T>C | RRAGB | ENSG00000083750.13 | transcript | ENST00000374941.9 | protein_coding | 7/9 | chrX | 55753550 | |||||||
| chrX:55753955 | G | A | 3 | a0001c0001t0001g0090 a0001c0001t0001g0106 a0001c0001t0001g0107 |
3 | HG01255.hp1 HG02630.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.735+441G>A | RRAGB | ENSG00000083750.13 | transcript | ENST00000374941.9 | protein_coding | 7/9 | chrX | 55753955 | |||||||
| chrX:55754105 | C | T | 1 | a0001c0001t0001g0086 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.735+591C>T | RRAGB | ENSG00000083750.13 | transcript | ENST00000374941.9 | protein_coding | 7/9 | chrX | 55754105 | |||||||
| chrX:55754540 | C | A | 1 | a0001c0001t0001g0048 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.735+1026C>A | RRAGB | ENSG00000083750.13 | transcript | ENST00000374941.9 | protein_coding | 7/9 | chrX | 55754540 | |||||||
| chrX:55754624 | T | A | 4 | a0001c0001t0002g0167 a0001c0001t0002g0168 a0001c0001t0002g0169 others(1): Show |
4 | HG02109.hp1 HG02559.hp1 HG02622.hp2 others(1): Show |
intron_variant | MODIFIER | c.735+1110T>A | RRAGB | ENSG00000083750.13 | transcript | ENST00000374941.9 | protein_coding | 7/9 | chrX | 55754624 | |||||||
| chrX:55754639 | C | G | 8 | a0001c0001t0002g0008 a0001c0001t0002g0113 a0001c0001t0002g0114 others(5): Show |
12 | HG00738.hp1 HG01167.hp1 HG01169.hp1 others(9): Show |
intron_variant | MODIFIER | c.735+1125C>G | RRAGB | ENSG00000083750.13 | transcript | ENST00000374941.9 | protein_coding | 7/9 | chrX | 55754639 | |||||||
| chrX:55754799 | G | A | 2 | a0001c0001t0002g0124 a0001c0001t0002g0125 |
2 | HG03540.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.736-1042G>A | RRAGB | ENSG00000083750.13 | transcript | ENST00000374941.9 | protein_coding | 7/9 | chrX | 55754799 | |||||||
| chrX:55754806 | A | G | 1 | a0001c0001t0002g0141 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.736-1035A>G | RRAGB | ENSG00000083750.13 | transcript | ENST00000374941.9 | protein_coding | 7/9 | chrX | 55754806 | |||||||
| chrX:55754900 | AGTAACAA others(51): Show |
A | 1 | a0001c0001t0001g0065 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.736-940_736-883del others(58): Show |
RRAGB | ENSG00000083750.13 | transcript | ENST00000374941.9 | protein_coding | 7/9 | chrX | 55754900 | |||||||
| chrX:55755495 | T | C | 3 | a0001c0001t0001g0099 a0001c0001t0001g0104 a0001c0001t0001g0105 |
3 | HG00735.hp1 HG02257.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.736-346T>C | RRAGB | ENSG00000083750.13 | transcript | ENST00000374941.9 | protein_coding | 7/9 | chrX | 55755495 | |||||||
| chrX:55755501 | T | C | 1 | a0001c0001t0001g0040 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.736-340T>C | RRAGB | ENSG00000083750.13 | transcript | ENST00000374941.9 | protein_coding | 7/9 | chrX | 55755501 | |||||||
| chrX:55755621 | A | C | 1 | a0001c0001t0002g0118 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.736-220A>C | RRAGB | ENSG00000083750.13 | transcript | ENST00000374941.9 | protein_coding | 7/9 | chrX | 55755621 | |||||||
| chrX:55755643 | A | G | 1 | a0001c0001t0002g0140 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.736-198A>G | RRAGB | ENSG00000083750.13 | transcript | ENST00000374941.9 | protein_coding | 7/9 | chrX | 55755643 | |||||||
| chrX:55755790 | G | T | 1 | a0001c0001t0001g0088 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.736-51G>T | RRAGB | ENSG00000083750.13 | transcript | ENST00000374941.9 | protein_coding | 7/9 | chrX | 55755790 | |||||||
| chrX:55756098 | C | CGTTGTCC others(49): Show |
1 | a0001c0001t0001g0065 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.827+176_827+177ins others(56): Show |
RRAGB | ENSG00000083750.13 | transcript | ENST00000374941.9 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chrX | 55756098 | ||||||
| chrX:55756381 | A | G | 3 | a0001c0001t0002g0008 a0001c0001t0002g0115 a0001c0001t0002g0116 |
7 | HG02818.hp2 HG02886.hp1 HG02922.hp2 others(4): Show |
intron_variant | MODIFIER | c.827+449A>G | RRAGB | ENSG00000083750.13 | transcript | ENST00000374941.9 | protein_coding | 8/9 | chrX | 55756381 | |||||||
| chrX:55756855 | C | T | 3 | a0001c0001t0001g0069 a0001c0001t0001g0074 a0001c0001t0001g0075 |
3 | NA18951.hp2 NA18970.hp1 NA19056.hp1 |
intron_variant | MODIFIER | c.828-361C>T | RRAGB | ENSG00000083750.13 | transcript | ENST00000374941.9 | protein_coding | 8/9 | chrX | 55756855 | |||||||
| chrX:55757135 | CAA | C | 8 | a0001c0001t0002g0008 a0001c0001t0002g0113 a0001c0001t0002g0114 others(5): Show |
12 | HG00738.hp1 HG01167.hp1 HG01169.hp1 others(9): Show |
intron_variant | MODIFIER | c.828-78_828-77delAA | RRAGB | ENSG00000083750.13 | transcript | ENST00000374941.9 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chrX | 55757135 | ||||||
| chrX:55757576 | T | G | 1 | a0001c0001t0001g0079 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.943+245T>G | RRAGB | ENSG00000083750.13 | transcript | ENST00000374941.9 | protein_coding | 9/9 | chrX | 55757576 | |||||||
| chrX:55757621 | G | A | 64 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(61): Show |
120 | HG00280.hp1 HG00423.hp1 HG00544.hp2 others(117): Show |
intron_variant | MODIFIER | c.943+290G>A | RRAGB | ENSG00000083750.13 | transcript | ENST00000374941.9 | protein_coding | 9/9 | chrX | 55757621 | |||||||
| chrX:55757699 | A | G | 1 | a0001c0001t0001g0049 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.943+368A>G | RRAGB | ENSG00000083750.13 | transcript | ENST00000374941.9 | protein_coding | 9/9 | chrX | 55757699 | |||||||
| chrX:55757747 | A | G | 5 | a0001c0001t0001g0021 a0001c0001t0001g0108 a0001c0001t0001g0110 others(2): Show |
6 | HG02572.hp1 HG02809.hp2 HG02970.hp2 others(3): Show |
intron_variant | MODIFIER | c.943+416A>G | RRAGB | ENSG00000083750.13 | transcript | ENST00000374941.9 | protein_coding | 9/9 | chrX | 55757747 | |||||||
| chrX:55757783 | G | A | 1 | a0001c0001t0001g0070 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.943+452G>A | RRAGB | ENSG00000083750.13 | transcript | ENST00000374941.9 | protein_coding | 9/9 | chrX | 55757783 | |||||||
| chrX:55757962 | C | G | 1 | a0001c0001t0001g0095 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.944-284C>G | RRAGB | ENSG00000083750.13 | transcript | ENST00000374941.9 | protein_coding | 9/9 | chrX | 55757962 |