Item | Value |
---|---|
geneid | 8712 |
ensemblid | ENSG00000068985.5 |
hgncid | 4107 |
symbol | PAGE1 |
name | PAGE family member 1 |
refseq_nuc | NM_003785.4 |
refseq_prot | NP_003776.2 |
ensembl_nuc | ENST00000376150.4 |
ensembl_prot | ENSP00000365320.3 |
mane_status | MANE Select |
chr | chrX |
start | 49687447 |
end | 49695984 |
strand | - |
ver | v1.2 |
region | chrX:49687447-49695984 |
region5000 | chrX:49682447-49700984 |
regionname0 | PAGE1_chrX_49687447_49695984 |
regionname5000 | PAGE1_chrX_49682447_49700984 |
ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 1/1 | 146 | 314 | 69 | 44 | 159 | 9 | 31 | 126 | PAGE1_chrX_49682447_49700984 | PAGE1 | MGFLR others(141): Show |
chrX | 49682447 | 49700984 |
a0002 | 0/0 | 146 | 5 | 5 | 0 | 0 | 0 | 0 | 0 | PAGE1_chrX_49682447_49700984 | PAGE1 | MGFLR others(141): Show |
chrX | 49682447 | 49700984 |
a0003 | 0/0 | 146 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | PAGE1_chrX_49682447_49700984 | PAGE1 | MGFLR others(141): Show |
chrX | 49682447 | 49700984 |
a0004 | 0/0 | 146 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | PAGE1_chrX_49682447_49700984 | PAGE1 | MGFLR others(141): Show |
chrX | 49682447 | 49700984 |
a0005 | 0/0 | 146 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | PAGE1_chrX_49682447_49700984 | PAGE1 | MGFLR others(141): Show |
chrX | 49682447 | 49700984 |
achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 1/1 | 438 | 307 | 67 | 43 | 156 | 9 | 30 | PAGE1_chrX_49682447_49700984 | PAGE1 | ATGGG others(433): Show |
chrX | 49682447 | 49700984 | ||
a0001c0003 | 0/0 | 438 | 5 | 0 | 1 | 3 | 0 | 1 | PAGE1_chrX_49682447_49700984 | PAGE1 | ATGGG others(433): Show |
chrX | 49682447 | 49700984 | ||
a0001c0004 | 0/0 | 438 | 2 | 2 | 0 | 0 | 0 | 0 | PAGE1_chrX_49682447_49700984 | PAGE1 | ATGGG others(433): Show |
chrX | 49682447 | 49700984 | ||
a0002c0002 | 0/0 | 438 | 5 | 5 | 0 | 0 | 0 | 0 | PAGE1_chrX_49682447_49700984 | PAGE1 | ATGGG others(433): Show |
chrX | 49682447 | 49700984 | ||
a0003c0005 | 0/0 | 438 | 1 | 0 | 1 | 0 | 0 | 0 | PAGE1_chrX_49682447_49700984 | PAGE1 | ATGGG others(433): Show |
chrX | 49682447 | 49700984 | ||
a0004c0007 | 0/0 | 438 | 1 | 0 | 1 | 0 | 0 | 0 | PAGE1_chrX_49682447_49700984 | PAGE1 | ATGGG others(433): Show |
chrX | 49682447 | 49700984 | ||
a0005c0006 | 0/0 | 438 | 1 | 0 | 0 | 0 | 0 | 1 | PAGE1_chrX_49682447_49700984 | PAGE1 | ATGGG others(433): Show |
chrX | 49682447 | 49700984 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 1/1 | 659 | 295 | 56 | 42 | 156 | 9 | 30 | PAGE1_chrX_49682447_49700984 | PAGE1 | GAGAA others(654): Show |
chrX | 49682447 | 49700984 |
a0001c0001t0002 | 0/0 | 659 | 8 | 7 | 1 | 0 | 0 | 0 | PAGE1_chrX_49682447_49700984 | PAGE1 | GAGAA others(654): Show |
chrX | 49682447 | 49700984 |
a0001c0001t0003 | 0/0 | 659 | 4 | 4 | 0 | 0 | 0 | 0 | PAGE1_chrX_49682447_49700984 | PAGE1 | GAGAA others(654): Show |
chrX | 49682447 | 49700984 |
a0001c0003t0001 | 0/0 | 659 | 5 | 0 | 1 | 3 | 0 | 1 | PAGE1_chrX_49682447_49700984 | PAGE1 | GAGAA others(654): Show |
chrX | 49682447 | 49700984 |
a0001c0004t0001 | 0/0 | 659 | 2 | 2 | 0 | 0 | 0 | 0 | PAGE1_chrX_49682447_49700984 | PAGE1 | GAGAA others(654): Show |
chrX | 49682447 | 49700984 |
a0002c0002t0001 | 0/0 | 659 | 5 | 5 | 0 | 0 | 0 | 0 | PAGE1_chrX_49682447_49700984 | PAGE1 | GAGAA others(654): Show |
chrX | 49682447 | 49700984 |
a0003c0005t0001 | 0/0 | 659 | 1 | 0 | 1 | 0 | 0 | 0 | PAGE1_chrX_49682447_49700984 | PAGE1 | GAGAA others(654): Show |
chrX | 49682447 | 49700984 |
a0004c0007t0001 | 0/0 | 659 | 1 | 0 | 1 | 0 | 0 | 0 | PAGE1_chrX_49682447_49700984 | PAGE1 | GAGAA others(654): Show |
chrX | 49682447 | 49700984 |
a0005c0006t0001 | 0/0 | 659 | 1 | 0 | 0 | 0 | 0 | 1 | PAGE1_chrX_49682447_49700984 | PAGE1 | GAGAA others(654): Show |
chrX | 49682447 | 49700984 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0001 | 1/0 | 69 | 13 | 11 | 32 | 2 | 10 | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
a0001c0001t0001g0002 | 0/0 | 18 | 0 | 2 | 16 | 0 | 0 | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
a0001c0001t0001g0003 | 0/0 | 15 | 0 | 1 | 14 | 0 | 0 | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
a0001c0001t0001g0004 | 0/0 | 12 | 1 | 2 | 7 | 1 | 1 | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
a0001c0001t0001g0005 | 0/0 | 9 | 2 | 1 | 6 | 0 | 0 | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
a0001c0001t0001g0006 | 0/0 | 8 | 0 | 2 | 3 | 0 | 3 | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
a0001c0001t0001g0007 | 0/0 | 7 | 0 | 3 | 3 | 1 | 0 | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
a0001c0001t0001g0008 | 0/0 | 6 | 3 | 0 | 1 | 1 | 1 | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
a0001c0001t0001g0009 | 0/0 | 6 | 0 | 1 | 5 | 0 | 0 | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
a0001c0001t0001g0010 | 0/0 | 6 | 0 | 0 | 6 | 0 | 0 | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
a0001c0001t0001g0011 | 0/0 | 6 | 0 | 0 | 6 | 0 | 0 | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
a0001c0001t0001g0012 | 0/0 | 5 | 1 | 1 | 3 | 0 | 0 | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
a0001c0001t0001g0013 | 0/0 | 4 | 1 | 1 | 0 | 0 | 2 | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
a0001c0001t0001g0014 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
a0001c0001t0001g0015 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
a0001c0001t0001g0016 | 0/0 | 4 | 1 | 1 | 1 | 0 | 1 | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
a0001c0001t0001g0019 | 0/0 | 3 | 0 | 1 | 2 | 0 | 0 | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
a0001c0001t0001g0020 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
a0001c0001t0001g0021 | 0/0 | 3 | 2 | 0 | 1 | 0 | 0 | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
a0001c0001t0001g0025 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
a0001c0001t0001g0026 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
a0001c0001t0001g0027 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
a0001c0001t0001g0028 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
a0001c0001t0001g0029 | 0/0 | 2 | 1 | 0 | 0 | 1 | 0 | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
a0001c0001t0001g0030 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
a0001c0001t0001g0031 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
a0001c0001t0001g0032 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
a0001c0001t0001g0034 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
a0001c0001t0001g0035 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
a0001c0001t0001g0036 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
a0001c0001t0001g0037 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
a0001c0001t0001g0038 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
a0001c0001t0001g0039 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
a0001c0001t0001g0041 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
a0001c0001t0001g0042 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
a0001c0001t0001g0043 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
a0001c0001t0001g0045 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
a0001c0001t0001g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
a0001c0001t0001g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
a0001c0001t0001g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
a0001c0001t0001g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
a0001c0001t0001g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
a0001c0001t0001g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
a0001c0001t0001g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
a0001c0001t0001g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
a0001c0001t0001g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
a0001c0001t0001g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
a0001c0001t0001g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
a0001c0001t0001g0062 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
a0001c0001t0001g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
a0001c0001t0001g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
a0001c0001t0001g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
a0001c0001t0001g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
a0001c0001t0001g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
a0001c0001t0001g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
a0001c0001t0001g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
a0001c0001t0001g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
a0001c0001t0001g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
a0001c0001t0001g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
a0001c0001t0001g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
a0001c0001t0001g0074 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
a0001c0001t0001g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
a0001c0001t0001g0076 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
a0001c0001t0001g0077 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
a0001c0001t0001g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
a0001c0001t0001g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
a0001c0001t0001g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
a0001c0001t0001g0081 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
a0001c0001t0001g0082 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
a0001c0001t0001g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
a0001c0001t0001g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
a0001c0001t0001g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
a0001c0001t0001g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
a0001c0001t0001g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
a0001c0001t0001g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
a0001c0001t0001g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
a0001c0001t0001g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
a0001c0001t0001g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
a0001c0001t0001g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
a0001c0001t0001g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
a0001c0001t0001g0095 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
a0001c0001t0001g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
a0001c0001t0001g0097 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
a0001c0001t0001g0098 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
a0001c0001t0001g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
a0001c0001t0001g0100 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
a0001c0001t0001g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
a0001c0001t0001g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
a0001c0001t0001g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
a0001c0001t0001g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
a0001c0001t0001g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
a0001c0001t0001g0106 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
a0001c0001t0001g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
a0001c0001t0001g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
a0001c0001t0001g0109 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
a0001c0001t0001g0110 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
a0001c0001t0001g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
a0001c0001t0001g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
a0001c0001t0001g0113 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
a0001c0001t0001g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
a0001c0001t0001g0115 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
a0001c0001t0001g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
a0001c0001t0001g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
a0001c0001t0001g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
a0001c0001t0001g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
a0001c0001t0001g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
a0001c0001t0001g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
a0001c0001t0001g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
a0001c0001t0002g0018 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
a0001c0001t0002g0023 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
a0001c0001t0002g0024 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
a0001c0001t0002g0040 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
a0001c0001t0003g0017 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
a0001c0003t0001g0022 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
a0001c0003t0001g0123 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
a0001c0003t0001g0124 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
a0001c0004t0001g0033 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
a0002c0002t0001g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
a0002c0002t0001g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
a0002c0002t0001g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
a0002c0002t0001g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
a0002c0002t0001g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
a0003c0005t0001g0044 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
a0004c0007t0001g0125 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
a0005c0006t0001g0088 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0001 | c0001 | t0001 | g0110 | EUR | GBR | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
HG00099 | hp2 | a0001 | c0001 | t0001 | g0097 | EUR | GBR | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
HG00140 | hp1 | a0001 | c0001 | t0001 | g0007 | EUR | GBR | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
HG00280 | hp1 | a0001 | c0001 | t0001 | g0004 | EUR | FIN | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
HG00323 | hp1 | a0001 | c0001 | t0001 | g0029 | EUR | FIN | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
HG00323 | hp2 | a0001 | c0001 | t0001 | g0008 | EUR | FIN | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
HG00408 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
HG00408 | hp2 | a0001 | c0001 | t0001 | g0120 | EAS | CHS | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
HG00423 | hp1 | a0001 | c0001 | t0001 | g0085 | EAS | CHS | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
HG00423 | hp2 | a0001 | c0001 | t0001 | g0021 | EAS | CHS | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
HG00438 | hp1 | a0001 | c0001 | t0001 | g0038 | EAS | CHS | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
HG00438 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | CHS | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
HG00544 | hp1 | a0001 | c0001 | t0001 | g0118 | EAS | CHS | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
HG00544 | hp2 | a0001 | c0001 | t0001 | g0122 | EAS | CHS | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
HG00558 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | CHS | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
HG00558 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
HG00597 | hp1 | a0001 | c0001 | t0001 | g0108 | EAS | CHS | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
HG00597 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | CHS | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
HG00609 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
HG00621 | hp1 | a0001 | c0001 | t0001 | g0019 | EAS | CHS | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
HG00639 | hp1 | a0003 | c0005 | t0001 | g0044 | AMR | PUR | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
HG00639 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
HG00642 | hp1 | a0001 | c0001 | t0001 | g0020 | AMR | PUR | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
HG00673 | hp1 | a0001 | c0001 | t0001 | g0038 | EAS | CHS | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
HG00733 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
HG00733 | hp2 | a0001 | c0001 | t0001 | g0036 | AMR | PUR | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
HG00735 | hp1 | a0001 | c0001 | t0001 | g0030 | AMR | PUR | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
HG00735 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
HG00738 | hp1 | a0001 | c0001 | t0001 | g0043 | AMR | PUR | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
HG00741 | hp1 | a0001 | c0001 | t0001 | g0106 | AMR | PUR | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
HG00741 | hp2 | a0001 | c0001 | t0001 | g0016 | AMR | PUR | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
HG01069 | hp1 | a0001 | c0001 | t0001 | g0006 | AMR | PUR | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
HG01070 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
HG01070 | hp2 | a0001 | c0001 | t0001 | g0009 | AMR | PUR | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
HG01074 | hp1 | a0004 | c0007 | t0001 | g0125 | AMR | PUR | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
HG01081 | hp1 | a0001 | c0001 | t0002 | g0040 | AMR | PUR | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
HG01081 | hp2 | a0001 | c0001 | t0001 | g0020 | AMR | PUR | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
HG01099 | hp1 | a0001 | c0001 | t0001 | g0013 | AMR | PUR | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
HG01106 | hp1 | a0001 | c0001 | t0001 | g0077 | AMR | PUR | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
HG01109 | hp1 | a0001 | c0001 | t0001 | g0004 | AMR | PUR | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
HG01167 | hp1 | a0001 | c0001 | t0001 | g0032 | AMR | PUR | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
HG01168 | hp1 | a0001 | c0001 | t0001 | g0095 | AMR | PUR | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
HG01168 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
HG01192 | hp1 | a0001 | c0001 | t0001 | g0031 | AMR | PUR | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
HG01243 | hp1 | a0001 | c0001 | t0001 | g0113 | AMR | PUR | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
HG01255 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
HG01256 | hp1 | a0001 | c0001 | t0001 | g0004 | AMR | CLM | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
HG01258 | hp1 | a0001 | c0001 | t0001 | g0007 | AMR | CLM | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
HG01261 | hp1 | a0001 | c0001 | t0001 | g0007 | AMR | CLM | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
HG01358 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
HG01361 | hp1 | a0001 | c0001 | t0001 | g0045 | AMR | CLM | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
HG01361 | hp2 | a0001 | c0001 | t0001 | g0020 | AMR | CLM | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
HG01433 | hp1 | a0001 | c0001 | t0001 | g0005 | AMR | CLM | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
HG01515 | hp1 | a0001 | c0001 | t0001 | g0001 | EUR | IBS | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
HG01884 | hp1 | a0001 | c0001 | t0001 | g0005 | AFR | ACB | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
HG01884 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | ACB | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
HG01891 | hp1 | a0001 | c0001 | t0001 | g0004 | AFR | ACB | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
HG01891 | hp2 | a0001 | c0001 | t0001 | g0086 | AFR | ACB | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
HG01928 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
HG01934 | hp1 | a0001 | c0001 | t0001 | g0081 | AMR | PEL | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
HG01943 | hp1 | a0001 | c0001 | t0001 | g0007 | AMR | PEL | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
HG01952 | hp1 | a0001 | c0001 | t0001 | g0012 | AMR | PEL | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
HG01978 | hp1 | a0001 | c0003 | t0001 | g0124 | AMR | PEL | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
HG01978 | hp2 | a0001 | c0001 | t0001 | g0006 | AMR | PEL | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
HG01993 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
HG01993 | hp2 | a0001 | c0001 | t0001 | g0003 | AMR | PEL | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
HG02004 | hp1 | a0001 | c0001 | t0001 | g0084 | AMR | PEL | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
HG02004 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
HG02015 | hp1 | a0001 | c0001 | t0001 | g0016 | EAS | KHV | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
HG02027 | hp1 | a0001 | c0001 | t0001 | g0073 | EAS | KHV | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
HG02040 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
HG02055 | hp1 | a0001 | c0001 | t0002 | g0024 | AFR | ACB | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
HG02056 | hp1 | a0001 | c0001 | t0001 | g0116 | EAS | KHV | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
HG02071 | hp1 | a0001 | c0001 | t0001 | g0114 | EAS | KHV | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
HG02074 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
HG02080 | hp1 | a0001 | c0001 | t0001 | g0030 | EAS | KHV | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
HG02080 | hp2 | a0001 | c0001 | t0001 | g0014 | EAS | KHV | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
HG02083 | hp1 | a0001 | c0001 | t0001 | g0012 | EAS | KHV | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
HG02129 | hp1 | a0001 | c0001 | t0001 | g0008 | EAS | KHV | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
HG02132 | hp1 | a0001 | c0001 | t0001 | g0046 | EAS | KHV | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
HG02135 | hp1 | a0001 | c0001 | t0001 | g0014 | EAS | KHV | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
HG02145 | hp1 | a0001 | c0001 | t0001 | g0064 | AFR | ACB | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
HG02155 | hp1 | a0001 | c0001 | t0001 | g0007 | EAS | CDX | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
HG02155 | hp2 | a0001 | c0001 | t0001 | g0112 | EAS | CDX | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
HG02257 | hp1 | a0001 | c0001 | t0001 | g0028 | AFR | ACB | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
HG02257 | hp2 | a0001 | c0001 | t0001 | g0026 | AFR | ACB | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
HG02258 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | ACB | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
HG02280 | hp1 | a0001 | c0001 | t0001 | g0016 | AFR | ACB | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
HG02280 | hp2 | a0001 | c0001 | t0001 | g0027 | AFR | ACB | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
HG02293 | hp1 | a0001 | c0001 | t0001 | g0019 | AMR | PEL | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
HG02293 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
HG02451 | hp1 | a0001 | c0001 | t0001 | g0056 | AFR | ACB | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
HG02451 | hp2 | a0001 | c0001 | t0001 | g0105 | AFR | ACB | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
HG02523 | hp1 | a0001 | c0001 | t0001 | g0009 | EAS | KHV | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
HG02523 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | KHV | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
HG02572 | hp1 | a0001 | c0001 | t0001 | g0079 | AFR | GWD | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
HG02602 | hp1 | a0001 | c0001 | t0001 | g0006 | SAS | PJL | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
HG02615 | hp1 | a0001 | c0001 | t0001 | g0008 | AFR | GWD | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
HG02615 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | GWD | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
HG02622 | hp1 | a0001 | c0001 | t0001 | g0054 | AFR | GWD | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
HG02622 | hp2 | a0002 | c0002 | t0001 | g0051 | AFR | GWD | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
HG02630 | hp1 | a0001 | c0001 | t0001 | g0028 | AFR | GWD | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
HG02630 | hp2 | a0001 | c0001 | t0001 | g0094 | AFR | GWD | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
HG02647 | hp1 | a0001 | c0004 | t0001 | g0033 | AFR | GWD | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
HG02683 | hp1 | a0001 | c0001 | t0001 | g0006 | SAS | PJL | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
HG02683 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
HG02698 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
HG02717 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | GWD | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
HG02723 | hp1 | a0001 | c0001 | t0002 | g0018 | AFR | GWD | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
HG02723 | hp2 | a0001 | c0001 | t0001 | g0027 | AFR | GWD | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
HG02735 | hp1 | a0001 | c0001 | t0001 | g0008 | SAS | PJL | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
HG02738 | hp1 | a0001 | c0001 | t0001 | g0004 | SAS | PJL | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
HG02809 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | GWD | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
HG02809 | hp2 | a0001 | c0001 | t0001 | g0015 | AFR | GWD | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
HG02818 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | GWD | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
HG02818 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | GWD | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
HG02886 | hp1 | a0001 | c0001 | t0001 | g0087 | AFR | GWD | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
HG02886 | hp2 | a0001 | c0001 | t0001 | g0067 | AFR | GWD | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
HG02895 | hp1 | a0001 | c0001 | t0001 | g0015 | AFR | GWD | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
HG02896 | hp1 | a0001 | c0001 | t0003 | g0017 | AFR | GWD | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
HG02896 | hp2 | a0001 | c0001 | t0001 | g0034 | AFR | GWD | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
HG02897 | hp1 | a0001 | c0001 | t0001 | g0034 | AFR | GWD | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
HG02897 | hp2 | a0001 | c0001 | t0003 | g0017 | AFR | GWD | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
HG02922 | hp1 | a0001 | c0001 | t0001 | g0066 | AFR | ESN | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
HG02922 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | ESN | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
HG02965 | hp1 | a0002 | c0002 | t0001 | g0053 | AFR | ESN | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
HG02970 | hp1 | a0001 | c0001 | t0001 | g0021 | AFR | ESN | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
HG02970 | hp2 | a0001 | c0001 | t0001 | g0080 | AFR | ESN | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
HG02976 | hp1 | a0001 | c0001 | t0002 | g0018 | AFR | ESN | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
HG02976 | hp2 | a0001 | c0001 | t0001 | g0008 | AFR | ESN | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
HG03017 | hp1 | a0001 | c0001 | t0001 | g0042 | SAS | PJL | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
HG03041 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | GWD | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
HG03041 | hp2 | a0002 | c0002 | t0001 | g0050 | AFR | GWD | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
HG03098 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | MSL | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
HG03130 | hp1 | a0001 | c0001 | t0001 | g0015 | AFR | ESN | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
HG03139 | hp1 | a0002 | c0002 | t0001 | g0049 | AFR | ESN | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
HG03195 | hp1 | a0001 | c0001 | t0001 | g0059 | AFR | ESN | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
HG03195 | hp2 | a0001 | c0001 | t0001 | g0015 | AFR | ESN | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
HG03209 | hp1 | a0001 | c0001 | t0003 | g0017 | AFR | MSL | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
HG03225 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | MSL | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
HG03239 | hp1 | a0001 | c0001 | t0001 | g0098 | SAS | PJL | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
HG03239 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
HG03453 | hp1 | a0001 | c0001 | t0002 | g0024 | AFR | MSL | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
HG03453 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | MSL | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
HG03486 | hp1 | a0001 | c0001 | t0001 | g0072 | AFR | MSL | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
HG03486 | hp2 | a0001 | c0001 | t0001 | g0055 | AFR | MSL | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
HG03490 | hp1 | a0001 | c0001 | t0001 | g0074 | SAS | PJL | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
HG03491 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
HG03491 | hp2 | a0001 | c0001 | t0001 | g0100 | SAS | PJL | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
HG03492 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
HG03516 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | ESN | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
HG03516 | hp2 | a0001 | c0001 | t0001 | g0005 | AFR | ESN | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
HG03540 | hp1 | a0001 | c0001 | t0003 | g0017 | AFR | GWD | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
HG03540 | hp2 | a0001 | c0001 | t0001 | g0013 | AFR | GWD | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
HG03579 | hp1 | a0001 | c0001 | t0001 | g0021 | AFR | MSL | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
HG03654 | hp1 | a0001 | c0001 | t0001 | g0013 | SAS | PJL | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
HG03669 | hp1 | a0001 | c0001 | t0001 | g0039 | SAS | PJL | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
HG03669 | hp2 | a0001 | c0001 | t0001 | g0062 | SAS | PJL | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
HG03688 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | STU | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
HG03704 | hp1 | a0001 | c0001 | t0001 | g0032 | SAS | PJL | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
HG03704 | hp2 | a0001 | c0003 | t0001 | g0123 | SAS | PJL | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
HG03710 | hp1 | a0001 | c0001 | t0001 | g0039 | SAS | PJL | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
HG03834 | hp1 | a0001 | c0001 | t0001 | g0016 | SAS | BEB | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
HG03834 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | BEB | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
HG03927 | hp1 | a0001 | c0001 | t0001 | g0109 | SAS | BEB | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
HG03927 | hp2 | a0001 | c0001 | t0001 | g0013 | SAS | BEB | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
HG03942 | hp1 | a0001 | c0001 | t0001 | g0041 | SAS | BEB | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
HG04115 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | STU | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
HG04184 | hp1 | a0005 | c0006 | t0001 | g0088 | SAS | BEB | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
HG04184 | hp2 | a0001 | c0001 | t0001 | g0006 | SAS | BEB | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
HG04199 | hp1 | a0001 | c0001 | t0001 | g0031 | SAS | STU | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
HG04204 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | STU | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
HG04228 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | STU | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
NA18522 | hp1 | a0001 | c0001 | t0001 | g0008 | AFR | YRI | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
NA18612 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CHB | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
NA18747 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | CHB | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
NA18939 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
NA18939 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
NA18941 | hp1 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
NA18941 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
NA18942 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
NA18942 | hp2 | a0001 | c0001 | t0001 | g0069 | EAS | JPT | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
NA18943 | hp1 | a0001 | c0001 | t0001 | g0103 | EAS | JPT | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
NA18944 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
NA18945 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
NA18946 | hp1 | a0001 | c0001 | t0001 | g0107 | EAS | JPT | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
NA18946 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
NA18947 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
NA18947 | hp2 | a0001 | c0001 | t0001 | g0091 | EAS | JPT | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
NA18948 | hp1 | a0001 | c0001 | t0001 | g0035 | EAS | JPT | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
NA18949 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
NA18949 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
NA18950 | hp1 | a0001 | c0003 | t0001 | g0022 | EAS | JPT | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
NA18950 | hp2 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
NA18951 | hp1 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
NA18951 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
NA18952 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
NA18953 | hp1 | a0001 | c0001 | t0001 | g0104 | EAS | JPT | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
NA18954 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
NA18954 | hp2 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
NA18956 | hp1 | a0001 | c0001 | t0001 | g0025 | EAS | JPT | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
NA18956 | hp2 | a0001 | c0001 | t0001 | g0121 | EAS | JPT | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
NA18959 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
NA18960 | hp1 | a0001 | c0001 | t0001 | g0092 | EAS | JPT | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
NA18961 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
NA18962 | hp1 | a0001 | c0001 | t0001 | g0037 | EAS | JPT | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
NA18963 | hp1 | a0001 | c0001 | t0001 | g0093 | EAS | JPT | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
NA18963 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
NA18964 | hp1 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
NA18964 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
NA18965 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
NA18966 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
NA18967 | hp1 | a0001 | c0001 | t0001 | g0025 | EAS | JPT | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
NA18968 | hp1 | a0001 | c0001 | t0001 | g0037 | EAS | JPT | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
NA18968 | hp2 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
NA18969 | hp1 | a0001 | c0001 | t0001 | g0014 | EAS | JPT | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
NA18969 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
NA18970 | hp1 | a0001 | c0001 | t0001 | g0035 | EAS | JPT | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
NA18971 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
NA18973 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
NA18973 | hp2 | a0001 | c0001 | t0001 | g0102 | EAS | JPT | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
NA18975 | hp1 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
NA18975 | hp2 | a0001 | c0001 | t0001 | g0014 | EAS | JPT | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
NA18977 | hp1 | a0001 | c0001 | t0001 | g0090 | EAS | JPT | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
NA18978 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
NA18978 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
NA18979 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
NA18979 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
NA18981 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
NA18981 | hp2 | a0001 | c0001 | t0001 | g0111 | EAS | JPT | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
NA18982 | hp1 | a0001 | c0001 | t0001 | g0061 | EAS | JPT | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
NA18983 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
NA18984 | hp1 | a0001 | c0001 | t0001 | g0047 | EAS | JPT | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
NA18986 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
NA18988 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
NA18989 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
NA18990 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
NA18992 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
NA18992 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
NA18993 | hp1 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
NA18993 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
NA18994 | hp1 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
NA18995 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
NA18999 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
NA18999 | hp2 | a0001 | c0003 | t0001 | g0022 | EAS | JPT | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
NA19000 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
NA19001 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
NA19001 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
NA19002 | hp1 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
NA19002 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
NA19003 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
NA19003 | hp2 | a0001 | c0001 | t0001 | g0096 | EAS | JPT | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
NA19004 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
NA19005 | hp1 | a0001 | c0001 | t0001 | g0117 | EAS | JPT | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
NA19006 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
NA19007 | hp1 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
NA19009 | hp1 | a0001 | c0001 | t0001 | g0036 | EAS | JPT | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
NA19010 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
NA19010 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
NA19011 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
NA19011 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
NA19012 | hp1 | a0001 | c0003 | t0001 | g0022 | EAS | JPT | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
NA19030 | hp1 | a0001 | c0001 | t0001 | g0026 | AFR | LWK | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
NA19030 | hp2 | a0001 | c0001 | t0002 | g0023 | AFR | LWK | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
NA19043 | hp1 | a0002 | c0002 | t0001 | g0052 | AFR | LWK | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
NA19054 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
NA19054 | hp2 | a0001 | c0001 | t0001 | g0099 | EAS | JPT | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
NA19055 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
NA19056 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
NA19058 | hp1 | a0001 | c0001 | t0001 | g0083 | EAS | JPT | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
NA19060 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
NA19062 | hp1 | a0001 | c0001 | t0001 | g0119 | EAS | JPT | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
NA19063 | hp1 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
NA19064 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
NA19064 | hp2 | a0001 | c0001 | t0001 | g0071 | EAS | JPT | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
NA19065 | hp1 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
NA19065 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
NA19066 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
NA19067 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
NA19068 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
NA19070 | hp1 | a0001 | c0001 | t0001 | g0101 | EAS | JPT | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
NA19072 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
NA19074 | hp1 | a0001 | c0001 | t0001 | g0019 | EAS | JPT | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
NA19074 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
NA19075 | hp1 | a0001 | c0001 | t0001 | g0089 | EAS | JPT | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
NA19076 | hp1 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
NA19078 | hp1 | a0001 | c0001 | t0001 | g0075 | EAS | JPT | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
NA19078 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
NA19079 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
NA19080 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
NA19080 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
NA19081 | hp1 | a0001 | c0001 | t0001 | g0048 | EAS | JPT | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
NA19081 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
NA19082 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
NA19083 | hp1 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
NA19085 | hp1 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
NA19086 | hp1 | a0001 | c0001 | t0001 | g0078 | EAS | JPT | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
NA19087 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
NA19087 | hp2 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
NA19088 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
NA19089 | hp1 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
NA19090 | hp1 | a0001 | c0001 | t0001 | g0065 | EAS | JPT | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
NA19090 | hp2 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
NA19091 | hp1 | a0001 | c0001 | t0001 | g0070 | EAS | JPT | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
NA20129 | hp1 | a0001 | c0001 | t0002 | g0018 | AFR | ASW | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
NA20129 | hp2 | a0001 | c0001 | t0001 | g0063 | AFR | ASW | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
NA20752 | hp1 | a0001 | c0001 | t0001 | g0082 | EUR | TSI | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
NA20805 | hp1 | a0001 | c0001 | t0001 | g0001 | EUR | TSI | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
NA20905 | hp1 | a0001 | c0001 | t0001 | g0115 | SAS | GIH | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
HG01123 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
HG01123 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
HG02109 | hp1 | a0001 | c0001 | t0001 | g0057 | AFR | ACB | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
HG02109 | hp2 | a0001 | c0001 | t0001 | g0058 | AFR | ACB | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
HG02486 | hp1 | a0001 | c0001 | t0001 | g0068 | AFR | ACB | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
HG03471 | hp1 | a0001 | c0001 | t0001 | g0060 | AFR | MSL | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
HG06807 | hp1 | a0001 | c0001 | t0002 | g0023 | AFR | USA | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
HG06807 | hp2 | a0001 | c0004 | t0001 | g0033 | AFR | USA | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
NA18955 | hp1 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
NA21309 | hp1 | a0001 | c0001 | t0001 | g0029 | AFR | LWK | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
NA21309 | hp2 | a0001 | c0001 | t0001 | g0012 | AFR | LWK | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
homoSapiens | chm13v2 | a0001 | c0001 | t0001 | g0076 | REF | REF | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
homoSapiens | grch38p0 | a0001 | c0001 | t0001 | g0001 | REF | REF | PAGE1_chrX_49682447_49700984 | PAGE1 | chrX | 49682447 | 49700984 |
view | chr:pos | ref | alt | # # of ahapid:amino-acid(protein) level |
ahapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chrX:49689423 | T | C | 1 | a0005 | 1 | HG04184.hp1 | missense_variant | MODERATE | c.413A>G | p.Glu138Gly | PAGE1 | ENSG00000068985.5 | transcript | ENST00000376150.4 | protein_coding | 5/6 | 537/659 | 413/441 | 138/146 | chrX | 49689423 | |||
chrX:49689453 | A | G | 1 | a0002 | 5 | HG02622.hp2 HG02965.hp1 HG03041.hp2 others(2): Show |
missense_variant | MODERATE | c.383T>C | p.Leu128Pro | PAGE1 | ENSG00000068985.5 | transcript | ENST00000376150.4 | protein_coding | 5/6 | 507/659 | 383/441 | 128/146 | chrX | 49689453 | |||
chrX:49694716 | A | T | 1 | a0003 | 1 | HG00639.hp1 | missense_variant | MODERATE | c.55T>A | p.Ser19Thr | PAGE1 | ENSG00000068985.5 | transcript | ENST00000376150.4 | protein_coding | 2/6 | 179/659 | 55/441 | 19/146 | chrX | 49694716 | |||
chrX:49694743 | G | A | 1 | a0004 | 1 | HG01074.hp1 | missense_variant | MODERATE | c.28C>T | p.Arg10Trp | PAGE1 | ENSG00000068985.5 | transcript | ENST00000376150.4 | protein_coding | 2/6 | 152/659 | 28/441 | 10/146 | chrX | 49694743 |
view | chr:pos | ref | alt | # # of chapid |
chapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chrX:49689527 | C | T | 1 | a0001c0004 | 2 | HG02647.hp1 HG06807.hp2 |
synonymous_variant | LOW | c.309G>A | p.Ala103Ala | PAGE1 | ENSG00000068985.5 | transcript | ENST00000376150.4 | protein_coding | 5/6 | 433/659 | 309/441 | 103/146 | chrX | 49689527 | |||
chrX:49694178 | G | A | 1 | a0001c0003 | 5 | HG01978.hp1 HG03704.hp2 NA18950.hp1 others(2): Show |
synonymous_variant | LOW | c.87C>T | p.Asp29Asp | PAGE1 | ENSG00000068985.5 | transcript | ENST00000376150.4 | protein_coding | 3/6 | 211/659 | 87/441 | 29/146 | chrX | 49694178 |
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:49695897 | G | A | 1 | a0001c0001t0003 | 4 | HG02896.hp1 HG02897.hp2 HG03209.hp1 others(1): Show |
5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-37C>T | PAGE1 | ENSG00000068985.5 | transcript | ENST00000376150.4 | protein_coding | 1/6 | chrX | 49695897 | |||||||
chrX:49695936 | C | T | 1 | a0001c0001t0002 | 8 | HG01081.hp1 HG02055.hp1 HG02723.hp1 others(5): Show |
5_prime_UTR_variant | MODIFIER | c.-76G>A | PAGE1 | ENSG00000068985.5 | transcript | ENST00000376150.4 | protein_coding | 1/6 | 1166 | chrX | 49695936 |
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:49687624 | A | G | 2 | a0001c0001t0001g0081 a0001c0001t0001g0094 |
2 | HG01934.hp1 HG02630.hp2 |
intron_variant | MODIFIER | c.419-61T>C | PAGE1 | ENSG00000068985.5 | transcript | ENST00000376150.4 | protein_coding | 5/5 | chrX | 49687624 | |||||||
chrX:49687690 | G | A | 1 | a0001c0001t0001g0114 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.419-127C>T | PAGE1 | ENSG00000068985.5 | transcript | ENST00000376150.4 | protein_coding | 5/5 | chrX | 49687690 | |||||||
chrX:49687706 | G | A | 9 | a0001c0001t0001g0003 a0001c0001t0001g0046 a0001c0001t0001g0047 others(6): Show |
23 | HG01993.hp2 HG02132.hp1 HG02622.hp2 others(20): Show |
intron_variant | MODIFIER | c.419-143C>T | PAGE1 | ENSG00000068985.5 | transcript | ENST00000376150.4 | protein_coding | 5/5 | chrX | 49687706 | |||||||
chrX:49688100 | T | G | 1 | a0001c0001t0001g0027 | 2 | HG02280.hp2 HG02723.hp2 |
intron_variant | MODIFIER | c.419-537A>C | PAGE1 | ENSG00000068985.5 | transcript | ENST00000376150.4 | protein_coding | 5/5 | chrX | 49688100 | |||||||
chrX:49688191 | C | A | 7 | a0001c0001t0001g0054 a0001c0001t0001g0055 a0001c0001t0001g0056 others(4): Show |
11 | HG01081.hp1 HG02055.hp1 HG02451.hp1 others(8): Show |
intron_variant | MODIFIER | c.419-628G>T | PAGE1 | ENSG00000068985.5 | transcript | ENST00000376150.4 | protein_coding | 5/5 | chrX | 49688191 | |||||||
chrX:49688230 | A | C | 6 | a0001c0001t0001g0015 a0001c0001t0001g0034 a0001c0001t0001g0086 others(3): Show |
11 | HG01243.hp1 HG01891.hp2 HG02647.hp1 others(8): Show |
intron_variant | MODIFIER | c.419-667T>G | PAGE1 | ENSG00000068985.5 | transcript | ENST00000376150.4 | protein_coding | 5/5 | chrX | 49688230 | |||||||
chrX:49688234 | A | T | 1 | a0001c0001t0001g0097 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.419-671T>A | PAGE1 | ENSG00000068985.5 | transcript | ENST00000376150.4 | protein_coding | 5/5 | chrX | 49688234 | |||||||
chrX:49688694 | G | C | 1 | a0001c0001t0001g0087 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.418+724C>G | PAGE1 | ENSG00000068985.5 | transcript | ENST00000376150.4 | protein_coding | 5/5 | chrX | 49688694 | |||||||
chrX:49688733 | A | G | 5 | a0002c0002t0001g0049 a0002c0002t0001g0050 a0002c0002t0001g0051 others(2): Show |
5 | HG02622.hp2 HG02965.hp1 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.418+685T>C | PAGE1 | ENSG00000068985.5 | transcript | ENST00000376150.4 | protein_coding | 5/5 | chrX | 49688733 | |||||||
chrX:49689101 | T | C | 7 | a0001c0001t0001g0054 a0001c0001t0001g0055 a0001c0001t0001g0056 others(4): Show |
11 | HG01081.hp1 HG02055.hp1 HG02451.hp1 others(8): Show |
intron_variant | MODIFIER | c.418+317A>G | PAGE1 | ENSG00000068985.5 | transcript | ENST00000376150.4 | protein_coding | 5/5 | chrX | 49689101 | |||||||
chrX:49689546 | T | TA | 9 | a0001c0001t0001g0012 a0001c0001t0001g0037 a0001c0001t0001g0063 others(6): Show |
14 | HG00099.hp2 HG01952.hp1 HG02071.hp1 others(11): Show |
splice_region_variant&intron_variant | LOW | c.293-4dupT | PAGE1 | ENSG00000068985.5 | transcript | ENST00000376150.4 | protein_coding | 4/5 | chrX | 49689546 | |||||||
chrX:49689546 | T | TAA | 4 | a0001c0001t0001g0006 a0001c0001t0001g0029 a0001c0001t0001g0080 others(1): Show |
12 | HG00323.hp1 HG01069.hp1 HG01978.hp2 others(9): Show |
splice_region_variant&intron_variant | LOW | c.293-5_293-4dupTT | PAGE1 | ENSG00000068985.5 | transcript | ENST00000376150.4 | protein_coding | 4/5 | chrX | 49689546 | |||||||
chrX:49689546 | T | TAAA | 2 | a0001c0001t0001g0009 a0001c0001t0001g0102 |
7 | HG01070.hp2 HG02523.hp1 NA18955.hp1 others(4): Show |
splice_region_variant&intron_variant | LOW | c.293-6_293-4dupTTT | PAGE1 | ENSG00000068985.5 | transcript | ENST00000376150.4 | protein_coding | 4/5 | chrX | 49689546 | |||||||
chrX:49689546 | T | TAAAA | 6 | a0001c0001t0001g0007 a0001c0001t0001g0081 a0001c0001t0001g0084 others(3): Show |
12 | HG00140.hp1 HG01258.hp1 HG01261.hp1 others(9): Show |
splice_region_variant&intron_variant | LOW | c.293-7_293-4dupTTTT | PAGE1 | ENSG00000068985.5 | transcript | ENST00000376150.4 | protein_coding | 4/5 | chrX | 49689546 | |||||||
chrX:49689546 | TA | T | 8 | a0001c0001t0001g0032 a0001c0001t0001g0039 a0001c0001t0001g0069 others(5): Show |
11 | HG01167.hp1 HG01243.hp1 HG01891.hp2 others(8): Show |
splice_region_variant&intron_variant | LOW | c.293-4delT | PAGE1 | ENSG00000068985.5 | transcript | ENST00000376150.4 | protein_coding | 4/5 | chrX | 49689546 | |||||||
chrX:49689546 | TAAA | T | 7 | a0001c0001t0001g0015 a0001c0001t0001g0016 a0001c0001t0001g0054 others(4): Show |
15 | HG00741.hp2 HG02015.hp1 HG02280.hp1 others(12): Show |
splice_region_variant&intron_variant | LOW | c.293-6_293-4delTTT | PAGE1 | ENSG00000068985.5 | transcript | ENST00000376150.4 | protein_coding | 4/5 | chrX | 49689546 | |||||||
chrX:49689546 | TAAAAAAA others(3): Show |
T | 3 | a0002c0002t0001g0049 a0002c0002t0001g0050 a0002c0002t0001g0053 |
3 | HG02965.hp1 HG03041.hp2 HG03139.hp1 |
splice_region_variant&intron_variant | LOW | c.293-13_293-4delTTT others(7): Show |
PAGE1 | ENSG00000068985.5 | transcript | ENST00000376150.4 | protein_coding | 4/5 | chrX | 49689546 | |||||||
chrX:49689546 | TAAAAAAA others(13): Show |
T | 4 | a0001c0001t0001g0003 a0001c0001t0001g0046 a0001c0001t0001g0047 others(1): Show |
18 | HG01993.hp2 HG02132.hp1 NA18747.hp1 others(15): Show |
splice_region_variant&intron_variant | LOW | c.293-23_293-4delTTT others(17): Show |
PAGE1 | ENSG00000068985.5 | transcript | ENST00000376150.4 | protein_coding | 4/5 | chrX | 49689546 | |||||||
chrX:49689565 | AAAAAAAA others(5): Show |
A | 1 | a0001c0001t0001g0034 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.293-34_293-23delAT others(10): Show |
PAGE1 | ENSG00000068985.5 | transcript | ENST00000376150.4 | protein_coding | 4/5 | chrX | 49689565 | |||||||
chrX:49689565 | AAAAAAAA others(15): Show |
A | 1 | a0001c0001t0003g0017 | 2 | HG03209.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.293-44_293-23delAT others(20): Show |
PAGE1 | ENSG00000068985.5 | transcript | ENST00000376150.4 | protein_coding | 4/5 | chrX | 49689565 | |||||||
chrX:49689566 | AAAAAAAA others(8): Show |
A | 1 | a0001c0001t0001g0043 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.293-38_293-24delAT others(13): Show |
PAGE1 | ENSG00000068985.5 | transcript | ENST00000376150.4 | protein_coding | 4/5 | chrX | 49689566 | |||||||
chrX:49689566 | AAAAAAAA others(16): Show |
A | 1 | a0001c0001t0003g0017 | 2 | HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.293-46_293-24delAT others(21): Show |
PAGE1 | ENSG00000068985.5 | transcript | ENST00000376150.4 | protein_coding | 4/5 | chrX | 49689566 | |||||||
chrX:49689567 | A | T | 1 | a0002c0002t0001g0052 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.293-24T>A | PAGE1 | ENSG00000068985.5 | transcript | ENST00000376150.4 | protein_coding | 4/5 | chrX | 49689567 | |||||||
chrX:49689568 | AAAAAAAA others(18): Show |
A | 1 | a0001c0001t0001g0059 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.293-50_293-26delAT others(23): Show |
PAGE1 | ENSG00000068985.5 | transcript | ENST00000376150.4 | protein_coding | 4/5 | chrX | 49689568 | |||||||
chrX:49689569 | A | T | 4 | a0002c0002t0001g0049 a0002c0002t0001g0050 a0002c0002t0001g0051 others(1): Show |
4 | HG02622.hp2 HG03041.hp2 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.293-26T>A | PAGE1 | ENSG00000068985.5 | transcript | ENST00000376150.4 | protein_coding | 4/5 | chrX | 49689569 | |||||||
chrX:49689569 | AAAAAAAA others(17): Show |
A | 2 | a0001c0001t0001g0058 a0001c0001t0001g0060 |
2 | HG02109.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.293-50_293-27delAT others(22): Show |
PAGE1 | ENSG00000068985.5 | transcript | ENST00000376150.4 | protein_coding | 4/5 | chrX | 49689569 | |||||||
chrX:49689570 | AAAAAAAT others(16): Show |
A | 1 | a0001c0001t0001g0026 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.293-50_293-28delAT others(21): Show |
PAGE1 | ENSG00000068985.5 | transcript | ENST00000376150.4 | protein_coding | 4/5 | chrX | 49689570 | |||||||
chrX:49689571 | A | T | 7 | a0001c0001t0001g0021 a0001c0001t0001g0067 a0002c0002t0001g0049 others(4): Show |
8 | HG02622.hp2 HG02886.hp2 HG02965.hp1 others(5): Show |
intron_variant | MODIFIER | c.293-28T>A | PAGE1 | ENSG00000068985.5 | transcript | ENST00000376150.4 | protein_coding | 4/5 | chrX | 49689571 | |||||||
chrX:49689571 | AAAAAATA others(15): Show |
A | 1 | a0001c0001t0001g0026 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.293-50_293-29delAT others(20): Show |
PAGE1 | ENSG00000068985.5 | transcript | ENST00000376150.4 | protein_coding | 4/5 | chrX | 49689571 | |||||||
chrX:49689572 | AAAAATAT others(12): Show |
A | 1 | a0001c0001t0001g0004 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.293-48_293-30delAT others(17): Show |
PAGE1 | ENSG00000068985.5 | transcript | ENST00000376150.4 | protein_coding | 4/5 | chrX | 49689572 | |||||||
chrX:49689572 | AAAAATAT others(16): Show |
A | 1 | a0001c0001t0001g0027 | 2 | HG02280.hp2 HG02723.hp2 |
intron_variant | MODIFIER | c.293-52_293-30delAT others(21): Show |
PAGE1 | ENSG00000068985.5 | transcript | ENST00000376150.4 | protein_coding | 4/5 | chrX | 49689572 | |||||||
chrX:49689573 | A | AATATATA others(7): Show |
1 | a0001c0001t0001g0109 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.293-31_293-30insAT others(12): Show |
PAGE1 | ENSG00000068985.5 | transcript | ENST00000376150.4 | protein_coding | 4/5 | chrX | 49689573 | |||||||
chrX:49689573 | A | AT | 3 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0021 |
3 | HG00423.hp2 HG03834.hp2 NA18969.hp2 |
intron_variant | MODIFIER | c.293-31_293-30insA | PAGE1 | ENSG00000068985.5 | transcript | ENST00000376150.4 | protein_coding | 4/5 | chrX | 49689573 | |||||||
chrX:49689573 | A | T | 17 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0011 others(14): Show |
19 | HG00099.hp1 HG00673.hp1 HG01891.hp2 others(16): Show |
intron_variant | MODIFIER | c.293-30T>A | PAGE1 | ENSG00000068985.5 | transcript | ENST00000376150.4 | protein_coding | 4/5 | chrX | 49689573 | |||||||
chrX:49689573 | AAAATATA others(15): Show |
A | 1 | a0001c0001t0001g0085 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.293-52_293-31delAT others(20): Show |
PAGE1 | ENSG00000068985.5 | transcript | ENST00000376150.4 | protein_coding | 4/5 | chrX | 49689573 | |||||||
chrX:49689573 | AAAATATA others(17): Show |
A | 2 | a0001c0001t0001g0002 a0001c0001t0001g0004 |
2 | HG00280.hp1 HG00735.hp2 |
intron_variant | MODIFIER | c.293-54_293-31delAT others(22): Show |
PAGE1 | ENSG00000068985.5 | transcript | ENST00000376150.4 | protein_coding | 4/5 | chrX | 49689573 | |||||||
chrX:49689574 | AAAT | A | 4 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(1): Show |
7 | HG00558.hp2 HG01255.hp1 HG02886.hp1 others(4): Show |
intron_variant | MODIFIER | c.293-34_293-32delAT others(1): Show |
PAGE1 | ENSG00000068985.5 | transcript | ENST00000376150.4 | protein_coding | 4/5 | chrX | 49689574 | |||||||
chrX:49689575 | A | AAAAAT | 3 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 |
8 | HG02523.hp2 NA18941.hp2 NA18942.hp1 others(5): Show |
intron_variant | MODIFIER | c.293-33_293-32insAT others(3): Show |
PAGE1 | ENSG00000068985.5 | transcript | ENST00000376150.4 | protein_coding | 4/5 | chrX | 49689575 | |||||||
chrX:49689575 | A | AAAAATAT others(4): Show |
1 | a0001c0001t0001g0001 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.293-33_293-32insAT others(9): Show |
PAGE1 | ENSG00000068985.5 | transcript | ENST00000376150.4 | protein_coding | 4/5 | chrX | 49689575 | |||||||
chrX:49689575 | A | AAAAT | 8 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0014 others(5): Show |
15 | HG00558.hp1 HG00609.hp1 HG00741.hp1 others(12): Show |
intron_variant | MODIFIER | c.293-33_293-32insAT others(2): Show |
PAGE1 | ENSG00000068985.5 | transcript | ENST00000376150.4 | protein_coding | 4/5 | chrX | 49689575 | |||||||
chrX:49689575 | A | AAAATATA others(5): Show |
1 | a0001c0001t0001g0001 | 2 | NA19055.hp1 NA19079.hp1 |
intron_variant | MODIFIER | c.293-33_293-32insAT others(10): Show |
PAGE1 | ENSG00000068985.5 | transcript | ENST00000376150.4 | protein_coding | 4/5 | chrX | 49689575 | |||||||
chrX:49689575 | A | AAAATATA others(9): Show |
1 | a0001c0001t0001g0001 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.293-33_293-32insAT others(14): Show |
PAGE1 | ENSG00000068985.5 | transcript | ENST00000376150.4 | protein_coding | 4/5 | chrX | 49689575 | |||||||
chrX:49689575 | A | AAAT | 7 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0008 others(4): Show |
16 | HG00735.hp1 HG01168.hp2 HG01515.hp1 others(13): Show |
intron_variant | MODIFIER | c.293-33_293-32insAT others(1): Show |
PAGE1 | ENSG00000068985.5 | transcript | ENST00000376150.4 | protein_coding | 4/5 | chrX | 49689575 | |||||||
chrX:49689575 | A | AAT | 6 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0008 others(3): Show |
7 | HG00597.hp2 HG02738.hp1 NA18522.hp1 others(4): Show |
intron_variant | MODIFIER | c.293-34_293-33dupAT | PAGE1 | ENSG00000068985.5 | transcript | ENST00000376150.4 | protein_coding | 4/5 | chrX | 49689575 | |||||||
chrX:49689575 | A | AATAT | 8 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0031 others(5): Show |
9 | HG00438.hp1 HG00544.hp1 HG02293.hp2 others(6): Show |
intron_variant | MODIFIER | c.293-36_293-33dupAT others(2): Show |
PAGE1 | ENSG00000068985.5 | transcript | ENST00000376150.4 | protein_coding | 4/5 | chrX | 49689575 | |||||||
chrX:49689575 | A | AATATATA others(3): Show |
1 | a0001c0001t0001g0011 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.293-42_293-33dupAT others(8): Show |
PAGE1 | ENSG00000068985.5 | transcript | ENST00000376150.4 | protein_coding | 4/5 | chrX | 49689575 | |||||||
chrX:49689575 | A | AATATATA others(5): Show |
1 | a0001c0001t0001g0013 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.293-44_293-33dupAT others(10): Show |
PAGE1 | ENSG00000068985.5 | transcript | ENST00000376150.4 | protein_coding | 4/5 | chrX | 49689575 | |||||||
chrX:49689575 | A | AT | 4 | a0001c0001t0001g0005 a0001c0001t0001g0008 a0001c0001t0001g0019 others(1): Show |
4 | HG02027.hp1 HG02615.hp1 NA18951.hp2 others(1): Show |
intron_variant | MODIFIER | c.293-33_293-32insA | PAGE1 | ENSG00000068985.5 | transcript | ENST00000376150.4 | protein_coding | 4/5 | chrX | 49689575 | |||||||
chrX:49689575 | A | T | 41 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(38): Show |
54 | HG00099.hp1 HG00408.hp2 HG00423.hp2 others(51): Show |
intron_variant | MODIFIER | c.293-32T>A | PAGE1 | ENSG00000068985.5 | transcript | ENST00000376150.4 | protein_coding | 4/5 | chrX | 49689575 | |||||||
chrX:49689575 | AAT | A | 5 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0010 others(2): Show |
8 | HG01884.hp2 HG03669.hp2 NA18939.hp1 others(5): Show |
intron_variant | MODIFIER | c.293-34_293-33delAT | PAGE1 | ENSG00000068985.5 | transcript | ENST00000376150.4 | protein_coding | 4/5 | chrX | 49689575 | |||||||
chrX:49689575 | AATATATA others(13): Show |
A | 1 | a0001c0001t0001g0057 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.293-52_293-33delAT others(18): Show |
PAGE1 | ENSG00000068985.5 | transcript | ENST00000376150.4 | protein_coding | 4/5 | chrX | 49689575 | |||||||
chrX:49689576 | AT | A | 5 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0019 others(2): Show |
5 | HG00639.hp2 HG00733.hp2 HG02293.hp1 others(2): Show |
intron_variant | MODIFIER | c.293-34delA | PAGE1 | ENSG00000068985.5 | transcript | ENST00000376150.4 | protein_coding | 4/5 | chrX | 49689576 | |||||||
chrX:49689576 | ATAT | A | 4 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0002g0024 others(1): Show |
4 | HG00639.hp1 HG01433.hp1 HG02055.hp1 others(1): Show |
intron_variant | MODIFIER | c.293-36_293-34delAT others(1): Show |
PAGE1 | ENSG00000068985.5 | transcript | ENST00000376150.4 | protein_coding | 4/5 | chrX | 49689576 | |||||||
chrX:49689576 | ATATATAT | A | 1 | a0001c0001t0001g0020 | 3 | HG00642.hp1 HG01081.hp2 HG01361.hp2 |
intron_variant | MODIFIER | c.293-40_293-34delAT others(5): Show |
PAGE1 | ENSG00000068985.5 | transcript | ENST00000376150.4 | protein_coding | 4/5 | chrX | 49689576 | |||||||
chrX:49689577 | T | A | 20 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0006 others(17): Show |
31 | HG00099.hp2 HG00621.hp1 HG01069.hp1 others(28): Show |
intron_variant | MODIFIER | c.293-34A>T | PAGE1 | ENSG00000068985.5 | transcript | ENST00000376150.4 | protein_coding | 4/5 | chrX | 49689577 | |||||||
chrX:49689579 | T | A | 11 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(8): Show |
20 | HG01109.hp1 HG01261.hp1 HG01361.hp1 others(17): Show |
intron_variant | MODIFIER | c.293-36A>T | PAGE1 | ENSG00000068985.5 | transcript | ENST00000376150.4 | protein_coding | 4/5 | chrX | 49689579 | |||||||
chrX:49689581 | T | A | 5 | a0001c0001t0001g0001 a0001c0001t0001g0012 a0001c0001t0001g0062 others(2): Show |
5 | HG00639.hp1 HG01952.hp1 HG02055.hp1 others(2): Show |
intron_variant | MODIFIER | c.293-38A>T | PAGE1 | ENSG00000068985.5 | transcript | ENST00000376150.4 | protein_coding | 4/5 | chrX | 49689581 | |||||||
chrX:49689583 | T | A | 2 | a0001c0001t0001g0055 a0001c0001t0002g0024 |
2 | HG03453.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.293-40A>T | PAGE1 | ENSG00000068985.5 | transcript | ENST00000376150.4 | protein_coding | 4/5 | chrX | 49689583 | |||||||
chrX:49689593 | T | C | 4 | a0001c0001t0001g0003 a0001c0001t0001g0046 a0001c0001t0001g0047 others(1): Show |
18 | HG01993.hp2 HG02132.hp1 NA18747.hp1 others(15): Show |
intron_variant | MODIFIER | c.293-50A>G | PAGE1 | ENSG00000068985.5 | transcript | ENST00000376150.4 | protein_coding | 4/5 | chrX | 49689593 | |||||||
chrX:49689597 | T | C | 1 | a0001c0001t0001g0054 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.293-54A>G | PAGE1 | ENSG00000068985.5 | transcript | ENST00000376150.4 | protein_coding | 4/5 | chrX | 49689597 | |||||||
chrX:49689599 | T | C | 2 | a0001c0001t0001g0054 a0002c0002t0001g0050 |
2 | HG02622.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.293-56A>G | PAGE1 | ENSG00000068985.5 | transcript | ENST00000376150.4 | protein_coding | 4/5 | chrX | 49689599 | |||||||
chrX:49689601 | T | C | 6 | a0001c0001t0001g0054 a0001c0001t0001g0055 a0002c0002t0001g0049 others(3): Show |
6 | HG02622.hp1 HG02622.hp2 HG02965.hp1 others(3): Show |
intron_variant | MODIFIER | c.293-58A>G | PAGE1 | ENSG00000068985.5 | transcript | ENST00000376150.4 | protein_coding | 4/5 | chrX | 49689601 | |||||||
chrX:49689603 | T | C | 5 | a0001c0001t0001g0054 a0001c0001t0001g0055 a0001c0001t0001g0056 others(2): Show |
5 | HG02451.hp1 HG02622.hp1 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.293-60A>G | PAGE1 | ENSG00000068985.5 | transcript | ENST00000376150.4 | protein_coding | 4/5 | chrX | 49689603 | |||||||
chrX:49689605 | T | C | 5 | a0001c0001t0001g0055 a0001c0001t0001g0056 a0002c0002t0001g0051 others(2): Show |
5 | HG02451.hp1 HG02622.hp2 HG02965.hp1 others(2): Show |
intron_variant | MODIFIER | c.293-62A>G | PAGE1 | ENSG00000068985.5 | transcript | ENST00000376150.4 | protein_coding | 4/5 | chrX | 49689605 | |||||||
chrX:49689607 | T | C | 8 | a0001c0001t0001g0054 a0001c0001t0001g0055 a0001c0001t0001g0056 others(5): Show |
12 | HG01081.hp1 HG02055.hp1 HG02451.hp1 others(9): Show |
intron_variant | MODIFIER | c.293-64A>G | PAGE1 | ENSG00000068985.5 | transcript | ENST00000376150.4 | protein_coding | 4/5 | chrX | 49689607 | |||||||
chrX:49689609 | T | C | 8 | a0001c0001t0001g0055 a0001c0001t0001g0056 a0001c0001t0002g0018 others(5): Show |
12 | HG01081.hp1 HG02055.hp1 HG02451.hp1 others(9): Show |
intron_variant | MODIFIER | c.293-66A>G | PAGE1 | ENSG00000068985.5 | transcript | ENST00000376150.4 | protein_coding | 4/5 | chrX | 49689609 | |||||||
chrX:49689611 | T | C | 9 | a0001c0001t0001g0003 a0001c0001t0001g0030 a0001c0001t0001g0046 others(6): Show |
24 | HG00735.hp1 HG01993.hp2 HG02080.hp1 others(21): Show |
intron_variant | MODIFIER | c.293-68A>G | PAGE1 | ENSG00000068985.5 | transcript | ENST00000376150.4 | protein_coding | 4/5 | chrX | 49689611 | |||||||
chrX:49689613 | C | T | 5 | a0002c0002t0001g0049 a0002c0002t0001g0050 a0002c0002t0001g0051 others(2): Show |
5 | HG02622.hp2 HG02965.hp1 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.293-70G>A | PAGE1 | ENSG00000068985.5 | transcript | ENST00000376150.4 | protein_coding | 4/5 | chrX | 49689613 | |||||||
chrX:49689619 | C | T | 5 | a0002c0002t0001g0049 a0002c0002t0001g0050 a0002c0002t0001g0051 others(2): Show |
5 | HG02622.hp2 HG02965.hp1 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.293-76G>A | PAGE1 | ENSG00000068985.5 | transcript | ENST00000376150.4 | protein_coding | 4/5 | chrX | 49689619 | |||||||
chrX:49689619 | CAT | C | 3 | a0001c0001t0001g0001 a0001c0001t0001g0065 a0001c0001t0001g0090 |
3 | NA18977.hp1 NA18983.hp1 NA19090.hp1 |
intron_variant | MODIFIER | c.293-78_293-77delAT | PAGE1 | ENSG00000068985.5 | transcript | ENST00000376150.4 | protein_coding | 4/5 | chrX | 49689619 | |||||||
chrX:49689629 | T | TAC | 4 | a0001c0001t0002g0018 a0001c0001t0002g0023 a0001c0001t0002g0024 others(1): Show |
8 | HG01081.hp1 HG02055.hp1 HG02723.hp1 others(5): Show |
intron_variant | MODIFIER | c.293-88_293-87dupGT | PAGE1 | ENSG00000068985.5 | transcript | ENST00000376150.4 | protein_coding | 4/5 | chrX | 49689629 | |||||||
chrX:49689631 | C | T | 4 | a0001c0001t0001g0003 a0001c0001t0001g0046 a0001c0001t0001g0047 others(1): Show |
18 | HG01993.hp2 HG02132.hp1 NA18747.hp1 others(15): Show |
intron_variant | MODIFIER | c.293-88G>A | PAGE1 | ENSG00000068985.5 | transcript | ENST00000376150.4 | protein_coding | 4/5 | chrX | 49689631 | |||||||
chrX:49689635 | T | C | 5 | a0001c0001t0001g0003 a0001c0001t0001g0046 a0001c0001t0001g0047 others(2): Show |
19 | HG00423.hp1 HG01993.hp2 HG02132.hp1 others(16): Show |
intron_variant | MODIFIER | c.293-92A>G | PAGE1 | ENSG00000068985.5 | transcript | ENST00000376150.4 | protein_coding | 4/5 | chrX | 49689635 | |||||||
chrX:49689642 | ATATGTGT others(3): Show |
A | 4 | a0001c0001t0001g0003 a0001c0001t0001g0046 a0001c0001t0001g0047 others(1): Show |
18 | HG01993.hp2 HG02132.hp1 NA18747.hp1 others(15): Show |
intron_variant | MODIFIER | c.293-109_293-100del others(10): Show |
PAGE1 | ENSG00000068985.5 | transcript | ENST00000376150.4 | protein_coding | 4/5 | chrX | 49689642 | |||||||
chrX:49689646 | G | A | 5 | a0002c0002t0001g0049 a0002c0002t0001g0050 a0002c0002t0001g0051 others(2): Show |
5 | HG02622.hp2 HG02965.hp1 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.293-103C>T | PAGE1 | ENSG00000068985.5 | transcript | ENST00000376150.4 | protein_coding | 4/5 | chrX | 49689646 | |||||||
chrX:49689648 | G | A | 5 | a0002c0002t0001g0049 a0002c0002t0001g0050 a0002c0002t0001g0051 others(2): Show |
5 | HG02622.hp2 HG02965.hp1 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.293-105C>T | PAGE1 | ENSG00000068985.5 | transcript | ENST00000376150.4 | protein_coding | 4/5 | chrX | 49689648 | |||||||
chrX:49689649 | T | TATAC | 5 | a0002c0002t0001g0049 a0002c0002t0001g0050 a0002c0002t0001g0051 others(2): Show |
5 | HG02622.hp2 HG02965.hp1 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.293-107_293-106ins others(4): Show |
PAGE1 | ENSG00000068985.5 | transcript | ENST00000376150.4 | protein_coding | 4/5 | chrX | 49689649 | |||||||
chrX:49689650 | G | A | 5 | a0002c0002t0001g0049 a0002c0002t0001g0050 a0002c0002t0001g0051 others(2): Show |
5 | HG02622.hp2 HG02965.hp1 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.293-107C>T | PAGE1 | ENSG00000068985.5 | transcript | ENST00000376150.4 | protein_coding | 4/5 | chrX | 49689650 | |||||||
chrX:49689652 | G | A | 5 | a0002c0002t0001g0049 a0002c0002t0001g0050 a0002c0002t0001g0051 others(2): Show |
5 | HG02622.hp2 HG02965.hp1 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.293-109C>T | PAGE1 | ENSG00000068985.5 | transcript | ENST00000376150.4 | protein_coding | 4/5 | chrX | 49689652 | |||||||
chrX:49689652 | GTA | G | 8 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0008 others(5): Show |
11 | HG00140.hp1 HG00323.hp2 HG00621.hp1 others(8): Show |
intron_variant | MODIFIER | c.293-111_293-110del others(2): Show |
PAGE1 | ENSG00000068985.5 | transcript | ENST00000376150.4 | protein_coding | 4/5 | chrX | 49689652 | |||||||
chrX:49689653 | T | C | 4 | a0001c0001t0001g0003 a0001c0001t0001g0046 a0001c0001t0001g0047 others(1): Show |
18 | HG01993.hp2 HG02132.hp1 NA18747.hp1 others(15): Show |
intron_variant | MODIFIER | c.293-110A>G | PAGE1 | ENSG00000068985.5 | transcript | ENST00000376150.4 | protein_coding | 4/5 | chrX | 49689653 | |||||||
chrX:49689654 | A | G | 11 | a0001c0001t0001g0011 a0001c0001t0001g0014 a0001c0001t0001g0025 others(8): Show |
24 | HG00423.hp1 HG00438.hp1 HG00673.hp1 others(21): Show |
intron_variant | MODIFIER | c.293-111T>C | PAGE1 | ENSG00000068985.5 | transcript | ENST00000376150.4 | protein_coding | 4/5 | chrX | 49689654 | |||||||
chrX:49689655 | T | C | 5 | a0002c0002t0001g0049 a0002c0002t0001g0050 a0002c0002t0001g0051 others(2): Show |
5 | HG02622.hp2 HG02965.hp1 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.293-112A>G | PAGE1 | ENSG00000068985.5 | transcript | ENST00000376150.4 | protein_coding | 4/5 | chrX | 49689655 | |||||||
chrX:49689663 | T | C | 1 | a0001c0001t0002g0024 | 2 | HG02055.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.293-120A>G | PAGE1 | ENSG00000068985.5 | transcript | ENST00000376150.4 | protein_coding | 4/5 | chrX | 49689663 | |||||||
chrX:49689663 | T | TAC | 3 | a0001c0001t0002g0018 a0001c0001t0002g0023 a0001c0001t0002g0040 |
6 | HG01081.hp1 HG02723.hp1 HG02976.hp1 others(3): Show |
intron_variant | MODIFIER | c.293-121_293-120ins others(2): Show |
PAGE1 | ENSG00000068985.5 | transcript | ENST00000376150.4 | protein_coding | 4/5 | chrX | 49689663 | |||||||
chrX:49689665 | T | C | 3 | a0001c0001t0001g0043 a0001c0001t0001g0054 a0001c0001t0001g0056 |
3 | HG00738.hp1 HG02451.hp1 HG02622.hp1 |
intron_variant | MODIFIER | c.293-122A>G | PAGE1 | ENSG00000068985.5 | transcript | ENST00000376150.4 | protein_coding | 4/5 | chrX | 49689665 | |||||||
chrX:49689667 | C | T | 7 | a0001c0001t0001g0043 a0001c0001t0001g0054 a0001c0001t0001g0056 others(4): Show |
11 | HG00738.hp1 HG01081.hp1 HG02055.hp1 others(8): Show |
intron_variant | MODIFIER | c.293-124G>A | PAGE1 | ENSG00000068985.5 | transcript | ENST00000376150.4 | protein_coding | 4/5 | chrX | 49689667 | |||||||
chrX:49689669 | T | C | 4 | a0001c0001t0002g0018 a0001c0001t0002g0023 a0001c0001t0002g0024 others(1): Show |
8 | HG01081.hp1 HG02055.hp1 HG02723.hp1 others(5): Show |
intron_variant | MODIFIER | c.293-126A>G | PAGE1 | ENSG00000068985.5 | transcript | ENST00000376150.4 | protein_coding | 4/5 | chrX | 49689669 | |||||||
chrX:49689671 | T | C | 3 | a0001c0001t0001g0043 a0001c0001t0001g0054 a0001c0001t0001g0056 |
3 | HG00738.hp1 HG02451.hp1 HG02622.hp1 |
intron_variant | MODIFIER | c.293-128A>G | PAGE1 | ENSG00000068985.5 | transcript | ENST00000376150.4 | protein_coding | 4/5 | chrX | 49689671 | |||||||
chrX:49689673 | C | CAT | 8 | a0001c0001t0001g0026 a0001c0001t0001g0027 a0001c0001t0001g0055 others(5): Show |
13 | HG02109.hp1 HG02109.hp2 HG02257.hp2 others(10): Show |
intron_variant | MODIFIER | c.293-132_293-131dup others(2): Show |
PAGE1 | ENSG00000068985.5 | transcript | ENST00000376150.4 | protein_coding | 4/5 | chrX | 49689673 | |||||||
chrX:49689673 | C | CATATATG others(19): Show |
2 | a0001c0001t0001g0031 a0001c0001t0001g0095 |
3 | HG01168.hp1 HG01192.hp1 HG04199.hp1 |
intron_variant | MODIFIER | c.293-156_293-131dup others(26): Show |
PAGE1 | ENSG00000068985.5 | transcript | ENST00000376150.4 | protein_coding | 4/5 | chrX | 49689673 | |||||||
chrX:49689673 | C | T | 7 | a0001c0001t0001g0043 a0001c0001t0001g0054 a0001c0001t0001g0056 others(4): Show |
11 | HG00738.hp1 HG01081.hp1 HG02055.hp1 others(8): Show |
intron_variant | MODIFIER | c.293-130G>A | PAGE1 | ENSG00000068985.5 | transcript | ENST00000376150.4 | protein_coding | 4/5 | chrX | 49689673 | |||||||
chrX:49689678 | A | ATG | 5 | a0002c0002t0001g0049 a0002c0002t0001g0050 a0002c0002t0001g0051 others(2): Show |
5 | HG02622.hp2 HG02965.hp1 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.293-137_293-136dup others(2): Show |
PAGE1 | ENSG00000068985.5 | transcript | ENST00000376150.4 | protein_coding | 4/5 | chrX | 49689678 | |||||||
chrX:49689678 | ATGTGTG | A | 4 | a0001c0001t0001g0003 a0001c0001t0001g0046 a0001c0001t0001g0047 others(1): Show |
18 | HG01993.hp2 HG02132.hp1 NA18747.hp1 others(15): Show |
intron_variant | MODIFIER | c.293-141_293-136del others(6): Show |
PAGE1 | ENSG00000068985.5 | transcript | ENST00000376150.4 | protein_coding | 4/5 | chrX | 49689678 | |||||||
chrX:49689686 | A | G | 4 | a0002c0002t0001g0050 a0002c0002t0001g0051 a0002c0002t0001g0052 others(1): Show |
4 | HG02622.hp2 HG02965.hp1 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.293-143T>C | PAGE1 | ENSG00000068985.5 | transcript | ENST00000376150.4 | protein_coding | 4/5 | chrX | 49689686 | |||||||
chrX:49689691 | T | C | 4 | a0001c0001t0001g0003 a0001c0001t0001g0046 a0001c0001t0001g0047 others(1): Show |
18 | HG01993.hp2 HG02132.hp1 NA18747.hp1 others(15): Show |
intron_variant | MODIFIER | c.293-148A>G | PAGE1 | ENSG00000068985.5 | transcript | ENST00000376150.4 | protein_coding | 4/5 | chrX | 49689691 | |||||||
chrX:49689695 | C | T | 9 | a0001c0001t0001g0003 a0001c0001t0001g0046 a0001c0001t0001g0047 others(6): Show |
23 | HG01993.hp2 HG02132.hp1 HG02622.hp2 others(20): Show |
intron_variant | MODIFIER | c.293-152G>A | PAGE1 | ENSG00000068985.5 | transcript | ENST00000376150.4 | protein_coding | 4/5 | chrX | 49689695 | |||||||
chrX:49689703 | T | C | 5 | a0002c0002t0001g0049 a0002c0002t0001g0050 a0002c0002t0001g0051 others(2): Show |
5 | HG02622.hp2 HG02965.hp1 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.293-160A>G | PAGE1 | ENSG00000068985.5 | transcript | ENST00000376150.4 | protein_coding | 4/5 | chrX | 49689703 | |||||||
chrX:49689706 | G | A | 4 | a0002c0002t0001g0050 a0002c0002t0001g0051 a0002c0002t0001g0052 others(1): Show |
4 | HG02622.hp2 HG02965.hp1 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.293-163C>T | PAGE1 | ENSG00000068985.5 | transcript | ENST00000376150.4 | protein_coding | 4/5 | chrX | 49689706 | |||||||
chrX:49689706 | GTGTATAT others(1): Show |
G | 21 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(18): Show |
35 | HG00099.hp2 HG00544.hp1 HG00558.hp1 others(32): Show |
intron_variant | MODIFIER | c.293-171_293-164del others(8): Show |
PAGE1 | ENSG00000068985.5 | transcript | ENST00000376150.4 | protein_coding | 4/5 | chrX | 49689706 | |||||||
chrX:49689708 | G | A | 4 | a0002c0002t0001g0050 a0002c0002t0001g0051 a0002c0002t0001g0052 others(1): Show |
4 | HG02622.hp2 HG02965.hp1 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.293-165C>T | PAGE1 | ENSG00000068985.5 | transcript | ENST00000376150.4 | protein_coding | 4/5 | chrX | 49689708 | |||||||
chrX:49689710 | A | G | 4 | a0001c0001t0001g0003 a0001c0001t0001g0046 a0001c0001t0001g0047 others(1): Show |
18 | HG01993.hp2 HG02132.hp1 NA18747.hp1 others(15): Show |
intron_variant | MODIFIER | c.293-167T>C | PAGE1 | ENSG00000068985.5 | transcript | ENST00000376150.4 | protein_coding | 4/5 | chrX | 49689710 | |||||||
chrX:49689712 | A | G | 8 | a0001c0001t0001g0003 a0001c0001t0001g0046 a0001c0001t0001g0047 others(5): Show |
22 | HG01993.hp2 HG02132.hp1 HG02622.hp2 others(19): Show |
intron_variant | MODIFIER | c.293-169T>C | PAGE1 | ENSG00000068985.5 | transcript | ENST00000376150.4 | protein_coding | 4/5 | chrX | 49689712 | |||||||
chrX:49689714 | A | G | 4 | a0002c0002t0001g0050 a0002c0002t0001g0051 a0002c0002t0001g0052 others(1): Show |
4 | HG02622.hp2 HG02965.hp1 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.293-171T>C | PAGE1 | ENSG00000068985.5 | transcript | ENST00000376150.4 | protein_coding | 4/5 | chrX | 49689714 | |||||||
chrX:49689716 | G | A | 4 | a0001c0001t0001g0003 a0001c0001t0001g0046 a0001c0001t0001g0047 others(1): Show |
18 | HG01993.hp2 HG02132.hp1 NA18747.hp1 others(15): Show |
intron_variant | MODIFIER | c.293-173C>T | PAGE1 | ENSG00000068985.5 | transcript | ENST00000376150.4 | protein_coding | 4/5 | chrX | 49689716 | |||||||
chrX:49689718 | A | G | 8 | a0001c0001t0002g0018 a0001c0001t0002g0023 a0001c0001t0002g0040 others(5): Show |
11 | HG01081.hp1 HG02622.hp2 HG02723.hp1 others(8): Show |
intron_variant | MODIFIER | c.293-175T>C | PAGE1 | ENSG00000068985.5 | transcript | ENST00000376150.4 | protein_coding | 4/5 | chrX | 49689718 | |||||||
chrX:49689722 | A | ATACACAC others(35): Show |
1 | a0001c0001t0001g0106 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.293-180_293-179ins others(42): Show |
PAGE1 | ENSG00000068985.5 | transcript | ENST00000376150.4 | protein_coding | 4/5 | chrX | 49689722 | |||||||
chrX:49689723 | T | C | 4 | a0001c0001t0001g0003 a0001c0001t0001g0046 a0001c0001t0001g0047 others(1): Show |
18 | HG01993.hp2 HG02132.hp1 NA18747.hp1 others(15): Show |
intron_variant | MODIFIER | c.293-180A>G | PAGE1 | ENSG00000068985.5 | transcript | ENST00000376150.4 | protein_coding | 4/5 | chrX | 49689723 | |||||||
chrX:49689724 | G | A | 12 | a0001c0001t0001g0003 a0001c0001t0001g0046 a0001c0001t0001g0047 others(9): Show |
29 | HG01081.hp1 HG01993.hp2 HG02132.hp1 others(26): Show |
intron_variant | MODIFIER | c.293-181C>T | PAGE1 | ENSG00000068985.5 | transcript | ENST00000376150.4 | protein_coding | 4/5 | chrX | 49689724 | |||||||
chrX:49689729 | T | C | 12 | a0001c0001t0001g0003 a0001c0001t0001g0046 a0001c0001t0001g0047 others(9): Show |
29 | HG01081.hp1 HG01993.hp2 HG02132.hp1 others(26): Show |
intron_variant | MODIFIER | c.293-186A>G | PAGE1 | ENSG00000068985.5 | transcript | ENST00000376150.4 | protein_coding | 4/5 | chrX | 49689729 | |||||||
chrX:49689733 | C | T | 12 | a0001c0001t0001g0003 a0001c0001t0001g0046 a0001c0001t0001g0047 others(9): Show |
29 | HG01081.hp1 HG01993.hp2 HG02132.hp1 others(26): Show |
intron_variant | MODIFIER | c.293-190G>A | PAGE1 | ENSG00000068985.5 | transcript | ENST00000376150.4 | protein_coding | 4/5 | chrX | 49689733 | |||||||
chrX:49689735 | C | T | 4 | a0001c0001t0001g0003 a0001c0001t0001g0046 a0001c0001t0001g0047 others(1): Show |
18 | HG01993.hp2 HG02132.hp1 NA18747.hp1 others(15): Show |
intron_variant | MODIFIER | c.293-192G>A | PAGE1 | ENSG00000068985.5 | transcript | ENST00000376150.4 | protein_coding | 4/5 | chrX | 49689735 | |||||||
chrX:49689737 | C | T | 12 | a0001c0001t0001g0003 a0001c0001t0001g0046 a0001c0001t0001g0047 others(9): Show |
29 | HG01081.hp1 HG01993.hp2 HG02132.hp1 others(26): Show |
intron_variant | MODIFIER | c.293-194G>A | PAGE1 | ENSG00000068985.5 | transcript | ENST00000376150.4 | protein_coding | 4/5 | chrX | 49689737 | |||||||
chrX:49689738 | A | G | 4 | a0001c0001t0001g0003 a0001c0001t0001g0046 a0001c0001t0001g0047 others(1): Show |
18 | HG01993.hp2 HG02132.hp1 NA18747.hp1 others(15): Show |
intron_variant | MODIFIER | c.293-195T>C | PAGE1 | ENSG00000068985.5 | transcript | ENST00000376150.4 | protein_coding | 4/5 | chrX | 49689738 | |||||||
chrX:49689740 | A | G | 4 | a0001c0001t0001g0003 a0001c0001t0001g0046 a0001c0001t0001g0047 others(1): Show |
18 | HG01993.hp2 HG02132.hp1 NA18747.hp1 others(15): Show |
intron_variant | MODIFIER | c.293-197T>C | PAGE1 | ENSG00000068985.5 | transcript | ENST00000376150.4 | protein_coding | 4/5 | chrX | 49689740 | |||||||
chrX:49689742 | A | G | 4 | a0001c0001t0001g0003 a0001c0001t0001g0046 a0001c0001t0001g0047 others(1): Show |
18 | HG01993.hp2 HG02132.hp1 NA18747.hp1 others(15): Show |
intron_variant | MODIFIER | c.293-199T>C | PAGE1 | ENSG00000068985.5 | transcript | ENST00000376150.4 | protein_coding | 4/5 | chrX | 49689742 | |||||||
chrX:49689744 | G | A | 4 | a0001c0001t0001g0106 a0001c0001t0002g0018 a0001c0001t0002g0023 others(1): Show |
7 | HG00741.hp1 HG01081.hp1 HG02723.hp1 others(4): Show |
intron_variant | MODIFIER | c.293-201C>T | PAGE1 | ENSG00000068985.5 | transcript | ENST00000376150.4 | protein_coding | 4/5 | chrX | 49689744 | |||||||
chrX:49689744 | G | GTA | 11 | a0001c0001t0001g0026 a0001c0001t0001g0027 a0001c0001t0001g0054 others(8): Show |
17 | HG02055.hp1 HG02109.hp1 HG02109.hp2 others(14): Show |
intron_variant | MODIFIER | c.293-203_293-202dup others(2): Show |
PAGE1 | ENSG00000068985.5 | transcript | ENST00000376150.4 | protein_coding | 4/5 | chrX | 49689744 | |||||||
chrX:49689744 | GTA | G | 5 | a0002c0002t0001g0049 a0002c0002t0001g0050 a0002c0002t0001g0051 others(2): Show |
5 | HG02622.hp2 HG02965.hp1 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.293-203_293-202del others(2): Show |
PAGE1 | ENSG00000068985.5 | transcript | ENST00000376150.4 | protein_coding | 4/5 | chrX | 49689744 | |||||||
chrX:49689746 | A | G | 3 | a0001c0001t0002g0018 a0001c0001t0002g0023 a0001c0001t0002g0040 |
6 | HG01081.hp1 HG02723.hp1 HG02976.hp1 others(3): Show |
intron_variant | MODIFIER | c.293-203T>C | PAGE1 | ENSG00000068985.5 | transcript | ENST00000376150.4 | protein_coding | 4/5 | chrX | 49689746 | |||||||
chrX:49689748 | A | G | 8 | a0001c0001t0002g0018 a0001c0001t0002g0023 a0001c0001t0002g0040 others(5): Show |
11 | HG01081.hp1 HG02622.hp2 HG02723.hp1 others(8): Show |
intron_variant | MODIFIER | c.293-205T>C | PAGE1 | ENSG00000068985.5 | transcript | ENST00000376150.4 | protein_coding | 4/5 | chrX | 49689748 | |||||||
chrX:49689750 | G | A | 4 | a0001c0001t0001g0003 a0001c0001t0001g0046 a0001c0001t0001g0047 others(1): Show |
18 | HG01993.hp2 HG02132.hp1 NA18747.hp1 others(15): Show |
intron_variant | MODIFIER | c.293-207C>T | PAGE1 | ENSG00000068985.5 | transcript | ENST00000376150.4 | protein_coding | 4/5 | chrX | 49689750 | |||||||
chrX:49689752 | G | A | 7 | a0001c0001t0001g0003 a0001c0001t0001g0046 a0001c0001t0001g0047 others(4): Show |
24 | HG01081.hp1 HG01993.hp2 HG02132.hp1 others(21): Show |
intron_variant | MODIFIER | c.293-209C>T | PAGE1 | ENSG00000068985.5 | transcript | ENST00000376150.4 | protein_coding | 4/5 | chrX | 49689752 | |||||||
chrX:49689755 | T | C | 4 | a0001c0001t0001g0003 a0001c0001t0001g0046 a0001c0001t0001g0047 others(1): Show |
18 | HG01993.hp2 HG02132.hp1 NA18747.hp1 others(15): Show |
intron_variant | MODIFIER | c.293-212A>G | PAGE1 | ENSG00000068985.5 | transcript | ENST00000376150.4 | protein_coding | 4/5 | chrX | 49689755 | |||||||
chrX:49689763 | T | C | 8 | a0001c0001t0002g0018 a0001c0001t0002g0023 a0001c0001t0002g0040 others(5): Show |
11 | HG01081.hp1 HG02622.hp2 HG02723.hp1 others(8): Show |
intron_variant | MODIFIER | c.293-220A>G | PAGE1 | ENSG00000068985.5 | transcript | ENST00000376150.4 | protein_coding | 4/5 | chrX | 49689763 | |||||||
chrX:49689765 | T | C | 5 | a0002c0002t0001g0049 a0002c0002t0001g0050 a0002c0002t0001g0051 others(2): Show |
5 | HG02622.hp2 HG02965.hp1 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.293-222A>G | PAGE1 | ENSG00000068985.5 | transcript | ENST00000376150.4 | protein_coding | 4/5 | chrX | 49689765 | |||||||
chrX:49689770 | G | A | 8 | a0001c0001t0002g0018 a0001c0001t0002g0023 a0001c0001t0002g0040 others(5): Show |
11 | HG01081.hp1 HG02622.hp2 HG02723.hp1 others(8): Show |
intron_variant | MODIFIER | c.293-227C>T | PAGE1 | ENSG00000068985.5 | transcript | ENST00000376150.4 | protein_coding | 4/5 | chrX | 49689770 | |||||||
chrX:49689776 | A | ATATATAC others(25): Show |
1 | a0001c0001t0001g0084 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.293-265_293-234dup others(32): Show |
PAGE1 | ENSG00000068985.5 | transcript | ENST00000376150.4 | protein_coding | 4/5 | chrX | 49689776 | |||||||
chrX:49689776 | A | ATATATGT others(7): Show |
3 | a0001c0001t0002g0018 a0001c0001t0002g0023 a0001c0001t0002g0040 |
6 | HG01081.hp1 HG02723.hp1 HG02976.hp1 others(3): Show |
intron_variant | MODIFIER | c.293-234_293-233ins others(14): Show |
PAGE1 | ENSG00000068985.5 | transcript | ENST00000376150.4 | protein_coding | 4/5 | chrX | 49689776 | |||||||
chrX:49689776 | A | G | 8 | a0001c0001t0001g0003 a0001c0001t0001g0046 a0001c0001t0001g0047 others(5): Show |
23 | HG01993.hp2 HG02055.hp1 HG02132.hp1 others(20): Show |
intron_variant | MODIFIER | c.293-233T>C | PAGE1 | ENSG00000068985.5 | transcript | ENST00000376150.4 | protein_coding | 4/5 | chrX | 49689776 | |||||||
chrX:49689780 | ATACACAC others(9): Show |
A | 5 | a0002c0002t0001g0049 a0002c0002t0001g0050 a0002c0002t0001g0051 others(2): Show |
5 | HG02622.hp2 HG02965.hp1 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.293-253_293-238del others(16): Show |
PAGE1 | ENSG00000068985.5 | transcript | ENST00000376150.4 | protein_coding | 4/5 | chrX | 49689780 | |||||||
chrX:49689783 | C | T | 7 | a0001c0001t0001g0003 a0001c0001t0001g0046 a0001c0001t0001g0047 others(4): Show |
24 | HG01081.hp1 HG01993.hp2 HG02132.hp1 others(21): Show |
intron_variant | MODIFIER | c.293-240G>A | PAGE1 | ENSG00000068985.5 | transcript | ENST00000376150.4 | protein_coding | 4/5 | chrX | 49689783 | |||||||
chrX:49689788 | A | C | 1 | a0001c0001t0001g0108 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.293-245T>G | PAGE1 | ENSG00000068985.5 | transcript | ENST00000376150.4 | protein_coding | 4/5 | chrX | 49689788 | |||||||
chrX:49689789 | T | C | 6 | a0001c0001t0001g0003 a0001c0001t0001g0047 a0001c0001t0001g0048 others(3): Show |
23 | HG01081.hp1 HG01993.hp2 HG02723.hp1 others(20): Show |
intron_variant | MODIFIER | c.293-246A>G | PAGE1 | ENSG00000068985.5 | transcript | ENST00000376150.4 | protein_coding | 4/5 | chrX | 49689789 | |||||||
chrX:49689794 | A | ATG | 4 | a0001c0001t0001g0054 a0001c0001t0001g0055 a0001c0001t0001g0056 others(1): Show |
5 | HG02055.hp1 HG02451.hp1 HG02622.hp1 others(2): Show |
intron_variant | MODIFIER | c.293-253_293-252dup others(2): Show |
PAGE1 | ENSG00000068985.5 | transcript | ENST00000376150.4 | protein_coding | 4/5 | chrX | 49689794 | |||||||
chrX:49689796 | GTA | G | 3 | a0001c0001t0002g0018 a0001c0001t0002g0023 a0001c0001t0002g0040 |
6 | HG01081.hp1 HG02723.hp1 HG02976.hp1 others(3): Show |
intron_variant | MODIFIER | c.293-255_293-254del others(2): Show |
PAGE1 | ENSG00000068985.5 | transcript | ENST00000376150.4 | protein_coding | 4/5 | chrX | 49689796 | |||||||
chrX:49689798 | A | G | 9 | a0001c0001t0001g0003 a0001c0001t0001g0046 a0001c0001t0001g0047 others(6): Show |
23 | HG01993.hp2 HG02132.hp1 HG02622.hp2 others(20): Show |
intron_variant | MODIFIER | c.293-255T>C | PAGE1 | ENSG00000068985.5 | transcript | ENST00000376150.4 | protein_coding | 4/5 | chrX | 49689798 | |||||||
chrX:49689804 | A | ATG | 1 | a0001c0001t0001g0020 | 3 | HG00642.hp1 HG01081.hp2 HG01361.hp2 |
intron_variant | MODIFIER | c.293-263_293-262dup others(2): Show |
PAGE1 | ENSG00000068985.5 | transcript | ENST00000376150.4 | protein_coding | 4/5 | chrX | 49689804 | |||||||
chrX:49689804 | A | ATGTGTAT others(25): Show |
1 | a0001c0001t0001g0112 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.293-293_293-262dup others(32): Show |
PAGE1 | ENSG00000068985.5 | transcript | ENST00000376150.4 | protein_coding | 4/5 | chrX | 49689804 | |||||||
chrX:49689804 | ATGTGTAT others(51): Show |
A | 1 | a0001c0001t0001g0046 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.293-319_293-262del others(58): Show |
PAGE1 | ENSG00000068985.5 | transcript | ENST00000376150.4 | protein_coding | 4/5 | chrX | 49689804 | |||||||
chrX:49689808 | G | A | 8 | a0001c0001t0001g0003 a0001c0001t0001g0047 a0001c0001t0001g0048 others(5): Show |
22 | HG01993.hp2 HG02622.hp2 HG02965.hp1 others(19): Show |
intron_variant | MODIFIER | c.293-265C>T | PAGE1 | ENSG00000068985.5 | transcript | ENST00000376150.4 | protein_coding | 4/5 | chrX | 49689808 | |||||||
chrX:49689812 | ATACACAC others(124): Show |
A | 3 | a0001c0001t0001g0003 a0001c0001t0001g0047 a0001c0001t0001g0048 |
17 | HG01993.hp2 NA18747.hp1 NA18946.hp2 others(14): Show |
intron_variant | MODIFIER | c.293-400_293-270del | PAGE1 | ENSG00000068985.5 | transcript | ENST00000376150.4 | protein_coding | 4/5 | chrX | 49689812 | |||||||
chrX:49689813 | T | TAC | 3 | a0001c0001t0001g0001 a0001c0001t0001g0012 a0001c0001t0001g0030 |
3 | HG00408.hp1 HG01952.hp1 HG02080.hp1 |
intron_variant | MODIFIER | c.293-272_293-271dup others(2): Show |
PAGE1 | ENSG00000068985.5 | transcript | ENST00000376150.4 | protein_coding | 4/5 | chrX | 49689813 | |||||||
chrX:49689815 | C | T | 3 | a0001c0001t0002g0018 a0001c0001t0002g0023 a0001c0001t0002g0040 |
6 | HG01081.hp1 HG02723.hp1 HG02976.hp1 others(3): Show |
intron_variant | MODIFIER | c.293-272G>A | PAGE1 | ENSG00000068985.5 | transcript | ENST00000376150.4 | protein_coding | 4/5 | chrX | 49689815 | |||||||
chrX:49689819 | C | CAT | 7 | a0001c0001t0001g0027 a0001c0001t0001g0054 a0001c0001t0001g0055 others(4): Show |
9 | HG02055.hp1 HG02109.hp2 HG02280.hp2 others(6): Show |
intron_variant | MODIFIER | c.293-278_293-277dup others(2): Show |
PAGE1 | ENSG00000068985.5 | transcript | ENST00000376150.4 | protein_coding | 4/5 | chrX | 49689819 | |||||||
chrX:49689819 | C | T | 3 | a0001c0001t0002g0018 a0001c0001t0002g0023 a0001c0001t0002g0040 |
6 | HG01081.hp1 HG02723.hp1 HG02976.hp1 others(3): Show |
intron_variant | MODIFIER | c.293-276G>A | PAGE1 | ENSG00000068985.5 | transcript | ENST00000376150.4 | protein_coding | 4/5 | chrX | 49689819 | |||||||
chrX:49689820 | ATATATGT others(1): Show |
A | 4 | a0001c0001t0001g0026 a0001c0001t0001g0043 a0001c0001t0001g0057 others(1): Show |
8 | HG00738.hp1 HG02109.hp1 HG02257.hp2 others(5): Show |
intron_variant | MODIFIER | c.293-285_293-278del others(8): Show |
PAGE1 | ENSG00000068985.5 | transcript | ENST00000376150.4 | protein_coding | 4/5 | chrX | 49689820 | |||||||
chrX:49689824 | ATG | A | 5 | a0002c0002t0001g0049 a0002c0002t0001g0050 a0002c0002t0001g0051 others(2): Show |
5 | HG02622.hp2 HG02965.hp1 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.293-283_293-282del others(2): Show |
PAGE1 | ENSG00000068985.5 | transcript | ENST00000376150.4 | protein_coding | 4/5 | chrX | 49689824 | |||||||
chrX:49689824 | ATGTGTAT others(5): Show |
A | 1 | a0001c0001t0001g0021 | 2 | HG02970.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.293-293_293-282del others(12): Show |
PAGE1 | ENSG00000068985.5 | transcript | ENST00000376150.4 | protein_coding | 4/5 | chrX | 49689824 | |||||||
chrX:49689826 | GTGTATAT others(1): Show |
G | 3 | a0001c0001t0002g0018 a0001c0001t0002g0023 a0001c0001t0002g0040 |
6 | HG01081.hp1 HG02723.hp1 HG02976.hp1 others(3): Show |
intron_variant | MODIFIER | c.293-291_293-284del others(8): Show |
PAGE1 | ENSG00000068985.5 | transcript | ENST00000376150.4 | protein_coding | 4/5 | chrX | 49689826 | |||||||
chrX:49689830 | A | G | 3 | a0001c0001t0001g0054 a0001c0001t0001g0055 a0001c0001t0001g0056 |
3 | HG02451.hp1 HG02622.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.293-287T>C | PAGE1 | ENSG00000068985.5 | transcript | ENST00000376150.4 | protein_coding | 4/5 | chrX | 49689830 | |||||||
chrX:49689836 | G | A | 4 | a0001c0001t0001g0054 a0001c0001t0001g0055 a0001c0001t0001g0056 others(1): Show |
5 | HG02055.hp1 HG02451.hp1 HG02622.hp1 others(2): Show |
intron_variant | MODIFIER | c.293-293C>T | PAGE1 | ENSG00000068985.5 | transcript | ENST00000376150.4 | protein_coding | 4/5 | chrX | 49689836 | |||||||
chrX:49689836 | G | GTGTGTAT others(3): Show |
4 | a0001c0001t0001g0027 a0001c0001t0001g0058 a0001c0001t0001g0059 others(1): Show |
5 | HG02109.hp2 HG02280.hp2 HG02723.hp2 others(2): Show |
intron_variant | MODIFIER | c.293-303_293-294dup others(10): Show |
PAGE1 | ENSG00000068985.5 | transcript | ENST00000376150.4 | protein_coding | 4/5 | chrX | 49689836 | |||||||
chrX:49689838 | GTGTATAT others(7): Show |
G | 4 | a0001c0001t0001g0026 a0001c0001t0001g0043 a0001c0001t0001g0057 others(1): Show |
8 | HG00738.hp1 HG02109.hp1 HG02257.hp2 others(5): Show |
intron_variant | MODIFIER | c.293-309_293-296del others(14): Show |
PAGE1 | ENSG00000068985.5 | transcript | ENST00000376150.4 | protein_coding | 4/5 | chrX | 49689838 | |||||||
chrX:49689847 | C | T | 5 | a0002c0002t0001g0049 a0002c0002t0001g0050 a0002c0002t0001g0051 others(2): Show |
5 | HG02622.hp2 HG02965.hp1 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.293-304G>A | PAGE1 | ENSG00000068985.5 | transcript | ENST00000376150.4 | protein_coding | 4/5 | chrX | 49689847 | |||||||
chrX:49689851 | C | CATATATA others(5): Show |
1 | a0001c0001t0001g0056 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.293-309_293-308ins others(12): Show |
PAGE1 | ENSG00000068985.5 | transcript | ENST00000376150.4 | protein_coding | 4/5 | chrX | 49689851 | |||||||
chrX:49689851 | C | T | 5 | a0002c0002t0001g0049 a0002c0002t0001g0050 a0002c0002t0001g0051 others(2): Show |
5 | HG02622.hp2 HG02965.hp1 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.293-308G>A | PAGE1 | ENSG00000068985.5 | transcript | ENST00000376150.4 | protein_coding | 4/5 | chrX | 49689851 | |||||||
chrX:49689858 | A | G | 5 | a0002c0002t0001g0049 a0002c0002t0001g0050 a0002c0002t0001g0051 others(2): Show |
5 | HG02622.hp2 HG02965.hp1 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.293-315T>C | PAGE1 | ENSG00000068985.5 | transcript | ENST00000376150.4 | protein_coding | 4/5 | chrX | 49689858 | |||||||
chrX:49689859 | G | T | 15 | a0001c0001t0001g0026 a0001c0001t0001g0043 a0001c0001t0001g0054 others(12): Show |
23 | HG00738.hp1 HG01081.hp1 HG02055.hp1 others(20): Show |
intron_variant | MODIFIER | c.293-316C>A | PAGE1 | ENSG00000068985.5 | transcript | ENST00000376150.4 | protein_coding | 4/5 | chrX | 49689859 | |||||||
chrX:49689863 | TGTATATA others(15): Show |
T | 1 | a0001c0001t0002g0024 | 2 | HG02055.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.293-342_293-321del others(22): Show |
PAGE1 | ENSG00000068985.5 | transcript | ENST00000376150.4 | protein_coding | 4/5 | chrX | 49689863 | |||||||
chrX:49689864 | G | A | 15 | a0001c0001t0001g0004 a0001c0001t0001g0027 a0001c0001t0001g0054 others(12): Show |
19 | HG00558.hp1 HG01081.hp1 HG02109.hp2 others(16): Show |
intron_variant | MODIFIER | c.293-321C>T | PAGE1 | ENSG00000068985.5 | transcript | ENST00000376150.4 | protein_coding | 4/5 | chrX | 49689864 | |||||||
chrX:49689870 | A | G | 1 | a0001c0001t0001g0004 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.293-327T>C | PAGE1 | ENSG00000068985.5 | transcript | ENST00000376150.4 | protein_coding | 4/5 | chrX | 49689870 | |||||||
chrX:49689874 | G | A | 1 | a0001c0001t0001g0046 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.293-331C>T | PAGE1 | ENSG00000068985.5 | transcript | ENST00000376150.4 | protein_coding | 4/5 | chrX | 49689874 | |||||||
chrX:49689885 | C | CATATATA others(5): Show |
1 | a0001c0001t0001g0054 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.293-343_293-342ins others(12): Show |
PAGE1 | ENSG00000068985.5 | transcript | ENST00000376150.4 | protein_coding | 4/5 | chrX | 49689885 | |||||||
chrX:49689885 | C | CATATATG others(3): Show |
1 | a0001c0001t0001g0056 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.293-343_293-342ins others(10): Show |
PAGE1 | ENSG00000068985.5 | transcript | ENST00000376150.4 | protein_coding | 4/5 | chrX | 49689885 | |||||||
chrX:49689892 | AGGTGTAT others(28): Show |
A | 1 | a0001c0001t0001g0001 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.293-384_293-350del others(35): Show |
PAGE1 | ENSG00000068985.5 | transcript | ENST00000376150.4 | protein_coding | 4/5 | chrX | 49689892 | |||||||
chrX:49689893 | G | T | 12 | a0001c0001t0001g0054 a0001c0001t0001g0055 a0001c0001t0001g0056 others(9): Show |
16 | HG01081.hp1 HG02055.hp1 HG02451.hp1 others(13): Show |
intron_variant | MODIFIER | c.293-350C>A | PAGE1 | ENSG00000068985.5 | transcript | ENST00000376150.4 | protein_coding | 4/5 | chrX | 49689893 | |||||||
chrX:49689898 | A | G | 8 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(5): Show |
11 | HG00558.hp1 HG01258.hp1 HG01884.hp1 others(8): Show |
intron_variant | MODIFIER | c.293-355T>C | PAGE1 | ENSG00000068985.5 | transcript | ENST00000376150.4 | protein_coding | 4/5 | chrX | 49689898 | |||||||
chrX:49689904 | A | ATG | 7 | a0001c0001t0001g0005 a0001c0001t0001g0015 a0001c0001t0001g0027 others(4): Show |
8 | HG02109.hp2 HG02280.hp2 HG02723.hp2 others(5): Show |
intron_variant | MODIFIER | c.293-363_293-362dup others(2): Show |
PAGE1 | ENSG00000068985.5 | transcript | ENST00000376150.4 | protein_coding | 4/5 | chrX | 49689904 | |||||||
chrX:49689904 | A | G | 2 | a0001c0001t0001g0001 a0001c0001t0001g0046 |
2 | HG02132.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.293-361T>C | PAGE1 | ENSG00000068985.5 | transcript | ENST00000376150.4 | protein_coding | 4/5 | chrX | 49689904 | |||||||
chrX:49689904 | ATGTGTAT others(30): Show |
A | 18 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(15): Show |
36 | HG00323.hp1 HG00544.hp1 HG01069.hp1 others(33): Show |
intron_variant | MODIFIER | c.293-398_293-362del others(37): Show |
PAGE1 | ENSG00000068985.5 | transcript | ENST00000376150.4 | protein_coding | 4/5 | chrX | 49689904 | |||||||
chrX:49689904 | ATGTGTAT others(66): Show |
A | 2 | a0001c0001t0001g0008 a0001c0001t0001g0064 |
2 | HG02145.hp1 HG02615.hp1 |
intron_variant | MODIFIER | c.293-434_293-362del others(73): Show |
PAGE1 | ENSG00000068985.5 | transcript | ENST00000376150.4 | protein_coding | 4/5 | chrX | 49689904 | |||||||
chrX:49689915 | C | T | 2 | a0001c0001t0001g0046 a0001c0001t0001g0055 |
2 | HG02132.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.293-372G>A | PAGE1 | ENSG00000068985.5 | transcript | ENST00000376150.4 | protein_coding | 4/5 | chrX | 49689915 | |||||||
chrX:49689916 | A | ATGTGTAT others(6): Show |
1 | a0001c0001t0001g0055 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.293-374_293-373ins others(13): Show |
PAGE1 | ENSG00000068985.5 | transcript | ENST00000376150.4 | protein_coding | 4/5 | chrX | 49689916 | |||||||
chrX:49689919 | C | T | 1 | a0001c0001t0001g0046 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.293-376G>A | PAGE1 | ENSG00000068985.5 | transcript | ENST00000376150.4 | protein_coding | 4/5 | chrX | 49689919 | |||||||
chrX:49689925 | TAGG | T | 3 | a0001c0001t0001g0046 a0001c0001t0001g0054 a0001c0001t0001g0055 |
3 | HG02132.hp1 HG02622.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.293-385_293-383del others(3): Show |
PAGE1 | ENSG00000068985.5 | transcript | ENST00000376150.4 | protein_coding | 4/5 | chrX | 49689925 | |||||||
chrX:49689926 | AG | A | 99 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(96): Show |
245 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(242): Show |
intron_variant | MODIFIER | c.293-384delC | PAGE1 | ENSG00000068985.5 | transcript | ENST00000376150.4 | protein_coding | 4/5 | chrX | 49689926 | |||||||
chrX:49689926 | AGGG | A | 5 | a0002c0002t0001g0049 a0002c0002t0001g0050 a0002c0002t0001g0051 others(2): Show |
5 | HG02622.hp2 HG02965.hp1 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.293-386_293-384del others(3): Show |
PAGE1 | ENSG00000068985.5 | transcript | ENST00000376150.4 | protein_coding | 4/5 | chrX | 49689926 | |||||||
chrX:49689926 | AGGGTGTA others(8): Show |
A | 1 | a0001c0001t0002g0024 | 2 | HG02055.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.293-398_293-384del others(15): Show |
PAGE1 | ENSG00000068985.5 | transcript | ENST00000376150.4 | protein_coding | 4/5 | chrX | 49689926 | |||||||
chrX:49689927 | G | GGTGTATA others(28): Show |
1 | a0001c0001t0001g0115 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.293-385_293-384ins others(35): Show |
PAGE1 | ENSG00000068985.5 | transcript | ENST00000376150.4 | protein_coding | 4/5 | chrX | 49689927 | |||||||
chrX:49689927 | G | T | 2 | a0001c0001t0001g0077 a0001c0001t0001g0097 |
2 | HG00099.hp2 HG01106.hp1 |
intron_variant | MODIFIER | c.293-384C>A | PAGE1 | ENSG00000068985.5 | transcript | ENST00000376150.4 | protein_coding | 4/5 | chrX | 49689927 | |||||||
chrX:49689927 | GGGTGTAT others(30): Show |
G | 5 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0011 others(2): Show |
6 | HG00558.hp2 HG03017.hp1 HG03927.hp1 others(3): Show |
intron_variant | MODIFIER | c.293-421_293-385del others(37): Show |
PAGE1 | ENSG00000068985.5 | transcript | ENST00000376150.4 | protein_coding | 4/5 | chrX | 49689927 | |||||||
chrX:49689928 | G | GTGTATAT others(28): Show |
2 | a0001c0001t0001g0077 a0001c0001t0001g0097 |
2 | HG00099.hp2 HG01106.hp1 |
intron_variant | MODIFIER | c.293-386_293-385ins others(35): Show |
PAGE1 | ENSG00000068985.5 | transcript | ENST00000376150.4 | protein_coding | 4/5 | chrX | 49689928 | |||||||
chrX:49689928 | G | T | 56 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(53): Show |
130 | HG00140.hp1 HG00323.hp2 HG00408.hp1 others(127): Show |
intron_variant | MODIFIER | c.293-385C>A | PAGE1 | ENSG00000068985.5 | transcript | ENST00000376150.4 | protein_coding | 4/5 | chrX | 49689928 | |||||||
chrX:49689933 | A | G | 6 | a0001c0001t0001g0046 a0002c0002t0001g0049 a0002c0002t0001g0050 others(3): Show |
6 | HG02132.hp1 HG02622.hp2 HG02965.hp1 others(3): Show |
intron_variant | MODIFIER | c.293-390T>C | PAGE1 | ENSG00000068985.5 | transcript | ENST00000376150.4 | protein_coding | 4/5 | chrX | 49689933 | |||||||
chrX:49689941 | G | A | 6 | a0001c0001t0001g0046 a0002c0002t0001g0049 a0002c0002t0001g0050 others(3): Show |
6 | HG02132.hp1 HG02622.hp2 HG02965.hp1 others(3): Show |
intron_variant | MODIFIER | c.293-398C>T | PAGE1 | ENSG00000068985.5 | transcript | ENST00000376150.4 | protein_coding | 4/5 | chrX | 49689941 | |||||||
chrX:49689941 | G | GTGTATAT others(3): Show |
2 | a0001c0001t0001g0054 a0001c0001t0001g0055 |
2 | HG02622.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.293-399_293-398ins others(10): Show |
PAGE1 | ENSG00000068985.5 | transcript | ENST00000376150.4 | protein_coding | 4/5 | chrX | 49689941 | |||||||
chrX:49689944 | TGTATATA others(5): Show |
T | 1 | a0001c0001t0001g0056 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.293-413_293-402del others(12): Show |
PAGE1 | ENSG00000068985.5 | transcript | ENST00000376150.4 | protein_coding | 4/5 | chrX | 49689944 | |||||||
chrX:49689945 | G | A | 3 | a0001c0001t0002g0018 a0001c0001t0002g0023 a0001c0001t0002g0040 |
6 | HG01081.hp1 HG02723.hp1 HG02976.hp1 others(3): Show |
intron_variant | MODIFIER | c.293-402C>T | PAGE1 | ENSG00000068985.5 | transcript | ENST00000376150.4 | protein_coding | 4/5 | chrX | 49689945 | |||||||
chrX:49689945 | GTATATAC others(19): Show |
G | 1 | a0001c0001t0001g0041 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.293-428_293-403del others(26): Show |
PAGE1 | ENSG00000068985.5 | transcript | ENST00000376150.4 | protein_coding | 4/5 | chrX | 49689945 | |||||||
chrX:49689950 | TACAC | T | 3 | a0001c0001t0002g0018 a0001c0001t0002g0023 a0001c0001t0002g0040 |
6 | HG01081.hp1 HG02723.hp1 HG02976.hp1 others(3): Show |
intron_variant | MODIFIER | c.293-411_293-408del others(4): Show |
PAGE1 | ENSG00000068985.5 | transcript | ENST00000376150.4 | protein_coding | 4/5 | chrX | 49689950 | |||||||
chrX:49689952 | C | T | 3 | a0001c0001t0001g0003 a0001c0001t0001g0047 a0001c0001t0001g0048 |
17 | HG01993.hp2 NA18747.hp1 NA18946.hp2 others(14): Show |
intron_variant | MODIFIER | c.293-409G>A | PAGE1 | ENSG00000068985.5 | transcript | ENST00000376150.4 | protein_coding | 4/5 | chrX | 49689952 | |||||||
chrX:49689956 | C | T | 3 | a0001c0001t0002g0018 a0001c0001t0002g0023 a0001c0001t0002g0040 |
6 | HG01081.hp1 HG02723.hp1 HG02976.hp1 others(3): Show |
intron_variant | MODIFIER | c.293-413G>A | PAGE1 | ENSG00000068985.5 | transcript | ENST00000376150.4 | protein_coding | 4/5 | chrX | 49689956 | |||||||
chrX:49689957 | A | G | 3 | a0001c0001t0002g0018 a0001c0001t0002g0023 a0001c0001t0002g0040 |
6 | HG01081.hp1 HG02723.hp1 HG02976.hp1 others(3): Show |
intron_variant | MODIFIER | c.293-414T>C | PAGE1 | ENSG00000068985.5 | transcript | ENST00000376150.4 | protein_coding | 4/5 | chrX | 49689957 | |||||||
chrX:49689958 | T | C | 3 | a0001c0001t0001g0003 a0001c0001t0001g0047 a0001c0001t0001g0048 |
17 | HG01993.hp2 NA18747.hp1 NA18946.hp2 others(14): Show |
intron_variant | MODIFIER | c.293-415A>G | PAGE1 | ENSG00000068985.5 | transcript | ENST00000376150.4 | protein_coding | 4/5 | chrX | 49689958 | |||||||
chrX:49689959 | A | G | 3 | a0001c0001t0002g0018 a0001c0001t0002g0023 a0001c0001t0002g0040 |
6 | HG01081.hp1 HG02723.hp1 HG02976.hp1 others(3): Show |
intron_variant | MODIFIER | c.293-416T>C | PAGE1 | ENSG00000068985.5 | transcript | ENST00000376150.4 | protein_coding | 4/5 | chrX | 49689959 | |||||||
chrX:49689964 | T | G | 9 | a0001c0001t0001g0021 a0001c0001t0001g0035 a0001c0001t0001g0038 others(6): Show |
13 | HG00423.hp2 HG00438.hp1 HG00673.hp1 others(10): Show |
intron_variant | MODIFIER | c.293-421A>C | PAGE1 | ENSG00000068985.5 | transcript | ENST00000376150.4 | protein_coding | 4/5 | chrX | 49689964 | |||||||
chrX:49689965 | G | A | 3 | a0001c0001t0002g0018 a0001c0001t0002g0023 a0001c0001t0002g0040 |
6 | HG01081.hp1 HG02723.hp1 HG02976.hp1 others(3): Show |
intron_variant | MODIFIER | c.293-422C>T | PAGE1 | ENSG00000068985.5 | transcript | ENST00000376150.4 | protein_coding | 4/5 | chrX | 49689965 | |||||||
chrX:49689965 | GTGTA | G | 3 | a0001c0001t0001g0003 a0001c0001t0001g0047 a0001c0001t0001g0048 |
17 | HG01993.hp2 NA18747.hp1 NA18946.hp2 others(14): Show |
intron_variant | MODIFIER | c.293-426_293-423del others(4): Show |
PAGE1 | ENSG00000068985.5 | transcript | ENST00000376150.4 | protein_coding | 4/5 | chrX | 49689965 | |||||||
chrX:49689966 | T | C | 3 | a0001c0001t0002g0018 a0001c0001t0002g0023 a0001c0001t0002g0040 |
6 | HG01081.hp1 HG02723.hp1 HG02976.hp1 others(3): Show |
intron_variant | MODIFIER | c.293-423A>G | PAGE1 | ENSG00000068985.5 | transcript | ENST00000376150.4 | protein_coding | 4/5 | chrX | 49689966 | |||||||
chrX:49689967 | G | A | 3 | a0001c0001t0002g0018 a0001c0001t0002g0023 a0001c0001t0002g0040 |
6 | HG01081.hp1 HG02723.hp1 HG02976.hp1 others(3): Show |
intron_variant | MODIFIER | c.293-424C>T | PAGE1 | ENSG00000068985.5 | transcript | ENST00000376150.4 | protein_coding | 4/5 | chrX | 49689967 | |||||||
chrX:49689968 | T | C | 3 | a0001c0001t0002g0018 a0001c0001t0002g0023 a0001c0001t0002g0040 |
6 | HG01081.hp1 HG02723.hp1 HG02976.hp1 others(3): Show |
intron_variant | MODIFIER | c.293-425A>G | PAGE1 | ENSG00000068985.5 | transcript | ENST00000376150.4 | protein_coding | 4/5 | chrX | 49689968 | |||||||
chrX:49689970 | T | C | 3 | a0001c0001t0002g0018 a0001c0001t0002g0023 a0001c0001t0002g0040 |
6 | HG01081.hp1 HG02723.hp1 HG02976.hp1 others(3): Show |
intron_variant | MODIFIER | c.293-427A>G | PAGE1 | ENSG00000068985.5 | transcript | ENST00000376150.4 | protein_coding | 4/5 | chrX | 49689970 | |||||||
chrX:49689975 | A | G | 1 | a0001c0001t0001g0090 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.293-432T>C | PAGE1 | ENSG00000068985.5 | transcript | ENST00000376150.4 | protein_coding | 4/5 | chrX | 49689975 | |||||||
chrX:49689977 | G | A | 4 | a0001c0001t0001g0056 a0001c0001t0002g0018 a0001c0001t0002g0023 others(1): Show |
7 | HG01081.hp1 HG02451.hp1 HG02723.hp1 others(4): Show |
intron_variant | MODIFIER | c.293-434C>T | PAGE1 | ENSG00000068985.5 | transcript | ENST00000376150.4 | protein_coding | 4/5 | chrX | 49689977 | |||||||
chrX:49689977 | G | GTGTATAT others(23): Show |
2 | a0001c0001t0001g0054 a0001c0001t0001g0055 |
2 | HG02622.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.293-435_293-434ins others(30): Show |
PAGE1 | ENSG00000068985.5 | transcript | ENST00000376150.4 | protein_coding | 4/5 | chrX | 49689977 | |||||||
chrX:49689977 | GTGTGTAT others(23): Show |
G | 1 | a0001c0001t0001g0090 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.293-464_293-435del others(30): Show |
PAGE1 | ENSG00000068985.5 | transcript | ENST00000376150.4 | protein_coding | 4/5 | chrX | 49689977 | |||||||
chrX:49689986 | TAC | T | 3 | a0001c0001t0001g0003 a0001c0001t0001g0047 a0001c0001t0001g0048 |
17 | HG01993.hp2 NA18747.hp1 NA18946.hp2 others(14): Show |
intron_variant | MODIFIER | c.293-445_293-444del others(2): Show |
PAGE1 | ENSG00000068985.5 | transcript | ENST00000376150.4 | protein_coding | 4/5 | chrX | 49689986 | |||||||
chrX:49689990 | C | T | 3 | a0001c0001t0001g0003 a0001c0001t0001g0047 a0001c0001t0001g0048 |
17 | HG01993.hp2 NA18747.hp1 NA18946.hp2 others(14): Show |
intron_variant | MODIFIER | c.293-447G>A | PAGE1 | ENSG00000068985.5 | transcript | ENST00000376150.4 | protein_coding | 4/5 | chrX | 49689990 | |||||||
chrX:49690005 | A | G | 3 | a0001c0001t0001g0003 a0001c0001t0001g0047 a0001c0001t0001g0048 |
17 | HG01993.hp2 NA18747.hp1 NA18946.hp2 others(14): Show |
intron_variant | MODIFIER | c.293-462T>C | PAGE1 | ENSG00000068985.5 | transcript | ENST00000376150.4 | protein_coding | 4/5 | chrX | 49690005 | |||||||
chrX:49690007 | A | ATATGTG | 6 | a0001c0001t0001g0036 a0001c0001t0001g0065 a0001c0001t0001g0083 others(3): Show |
7 | HG00597.hp1 HG00733.hp2 HG03491.hp2 others(4): Show |
intron_variant | MODIFIER | c.293-465_293-464ins others(6): Show |
PAGE1 | ENSG00000068985.5 | transcript | ENST00000376150.4 | protein_coding | 4/5 | chrX | 49690007 | |||||||
chrX:49690011 | A | G | 1 | a0001c0001t0001g0078 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.293-468T>C | PAGE1 | ENSG00000068985.5 | transcript | ENST00000376150.4 | protein_coding | 4/5 | chrX | 49690011 | |||||||
chrX:49690013 | G | A | 9 | a0001c0001t0001g0003 a0001c0001t0001g0036 a0001c0001t0001g0047 others(6): Show |
24 | HG00597.hp1 HG00733.hp2 HG01993.hp2 others(21): Show |
intron_variant | MODIFIER | c.293-470C>T | PAGE1 | ENSG00000068985.5 | transcript | ENST00000376150.4 | protein_coding | 4/5 | chrX | 49690013 | |||||||
chrX:49690013 | GTGTGTAT others(35): Show |
G | 5 | a0001c0001t0001g0057 a0001c0001t0001g0102 a0001c0001t0001g0103 others(2): Show |
5 | HG02109.hp1 NA18943.hp1 NA18973.hp2 others(2): Show |
intron_variant | MODIFIER | c.293-512_293-471del others(42): Show |
PAGE1 | ENSG00000068985.5 | transcript | ENST00000376150.4 | protein_coding | 4/5 | chrX | 49690013 | |||||||
chrX:49690015 | GTGTATAT others(81): Show |
G | 4 | a0002c0002t0001g0049 a0002c0002t0001g0050 a0002c0002t0001g0052 others(1): Show |
4 | HG02965.hp1 HG03041.hp2 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.293-560_293-473del others(88): Show |
PAGE1 | ENSG00000068985.5 | transcript | ENST00000376150.4 | protein_coding | 4/5 | chrX | 49690015 | |||||||
chrX:49690015 | GTGTATAT others(103): Show |
G | 1 | a0002c0002t0001g0051 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.293-582_293-473del | PAGE1 | ENSG00000068985.5 | transcript | ENST00000376150.4 | protein_coding | 4/5 | chrX | 49690015 | |||||||
chrX:49690016 | TGTATATA others(89): Show |
T | 1 | a0001c0001t0001g0046 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.293-569_293-474del others(96): Show |
PAGE1 | ENSG00000068985.5 | transcript | ENST00000376150.4 | protein_coding | 4/5 | chrX | 49690016 | |||||||
chrX:49690024 | C | T | 1 | a0001c0001t0002g0024 | 2 | HG02055.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.293-481G>A | PAGE1 | ENSG00000068985.5 | transcript | ENST00000376150.4 | protein_coding | 4/5 | chrX | 49690024 | |||||||
chrX:49690029 | ATATATAT others(3): Show |
A | 1 | a0001c0001t0001g0034 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.293-496_293-487del others(10): Show |
PAGE1 | ENSG00000068985.5 | transcript | ENST00000376150.4 | protein_coding | 4/5 | chrX | 49690029 | |||||||
chrX:49690041 | ATATATGT others(1): Show |
A | 3 | a0001c0001t0001g0003 a0001c0001t0001g0047 a0001c0001t0001g0048 |
17 | HG01993.hp2 NA18747.hp1 NA18946.hp2 others(14): Show |
intron_variant | MODIFIER | c.293-506_293-499del others(8): Show |
PAGE1 | ENSG00000068985.5 | transcript | ENST00000376150.4 | protein_coding | 4/5 | chrX | 49690041 | |||||||
chrX:49690043 | ATATGTG | A | 15 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0014 others(12): Show |
19 | HG01081.hp1 HG01884.hp1 HG01891.hp1 others(16): Show |
intron_variant | MODIFIER | c.293-506_293-501del others(6): Show |
PAGE1 | ENSG00000068985.5 | transcript | ENST00000376150.4 | protein_coding | 4/5 | chrX | 49690043 | |||||||
chrX:49690047 | G | A | 1 | a0001c0001t0001g0059 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.293-504C>T | PAGE1 | ENSG00000068985.5 | transcript | ENST00000376150.4 | protein_coding | 4/5 | chrX | 49690047 | |||||||
chrX:49690049 | G | GTGTGTAT others(23): Show |
1 | a0001c0001t0001g0059 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.293-507_293-506ins others(30): Show |
PAGE1 | ENSG00000068985.5 | transcript | ENST00000376150.4 | protein_coding | 4/5 | chrX | 49690049 | |||||||
chrX:49690055 | A | G | 16 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0014 others(13): Show |
20 | HG01081.hp1 HG01884.hp1 HG01891.hp1 others(17): Show |
intron_variant | MODIFIER | c.293-512T>C | PAGE1 | ENSG00000068985.5 | transcript | ENST00000376150.4 | protein_coding | 4/5 | chrX | 49690055 | |||||||
chrX:49690056 | T | C | 1 | a0001c0001t0001g0014 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.293-513A>G | PAGE1 | ENSG00000068985.5 | transcript | ENST00000376150.4 | protein_coding | 4/5 | chrX | 49690056 | |||||||
chrX:49690056 | TGTGTATA others(3): Show |
T | 1 | a0001c0001t0002g0024 | 2 | HG02055.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.293-523_293-514del others(10): Show |
PAGE1 | ENSG00000068985.5 | transcript | ENST00000376150.4 | protein_coding | 4/5 | chrX | 49690056 | |||||||
chrX:49690066 | C | T | 39 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(36): Show |
81 | HG00099.hp1 HG00280.hp1 HG00408.hp2 others(78): Show |
intron_variant | MODIFIER | c.293-523G>A | PAGE1 | ENSG00000068985.5 | transcript | ENST00000376150.4 | protein_coding | 4/5 | chrX | 49690066 | |||||||
chrX:49690070 | CAT | C | 3 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0062 |
3 | HG00140.hp1 HG01515.hp1 HG03669.hp2 |
intron_variant | MODIFIER | c.293-529_293-528del others(2): Show |
PAGE1 | ENSG00000068985.5 | transcript | ENST00000376150.4 | protein_coding | 4/5 | chrX | 49690070 | |||||||
chrX:49690071 | ATATATAT others(3): Show |
A | 3 | a0001c0001t0001g0006 a0001c0001t0001g0021 a0001c0001t0001g0086 |
5 | HG01891.hp2 HG02602.hp1 HG02683.hp1 others(2): Show |
intron_variant | MODIFIER | c.293-538_293-529del others(10): Show |
PAGE1 | ENSG00000068985.5 | transcript | ENST00000376150.4 | protein_coding | 4/5 | chrX | 49690071 | |||||||
chrX:49690071 | ATATATAT others(13): Show |
A | 32 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(29): Show |
66 | HG00099.hp1 HG00280.hp1 HG00408.hp2 others(63): Show |
intron_variant | MODIFIER | c.293-548_293-529del others(20): Show |
PAGE1 | ENSG00000068985.5 | transcript | ENST00000376150.4 | protein_coding | 4/5 | chrX | 49690071 | |||||||
chrX:49690081 | G | GTATATAC others(3): Show |
1 | a0001c0001t0001g0007 | 1 | HG01258.hp1 | intron_variant | MODIFIER | c.293-539_293-538ins others(10): Show |
PAGE1 | ENSG00000068985.5 | transcript | ENST00000376150.4 | protein_coding | 4/5 | chrX | 49690081 | |||||||
chrX:49690081 | GTATATAT others(47): Show |
G | 1 | a0001c0001t0001g0029 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.293-592_293-539del others(54): Show |
PAGE1 | ENSG00000068985.5 | transcript | ENST00000376150.4 | protein_coding | 4/5 | chrX | 49690081 | |||||||
chrX:49690082 | TATATATG others(23): Show |
T | 1 | a0001c0001t0002g0024 | 2 | HG02055.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.293-569_293-540del others(30): Show |
PAGE1 | ENSG00000068985.5 | transcript | ENST00000376150.4 | protein_coding | 4/5 | chrX | 49690082 | |||||||
chrX:49690083 | ATATATGT others(1): Show |
A | 3 | a0001c0001t0001g0003 a0001c0001t0001g0047 a0001c0001t0001g0048 |
17 | HG01993.hp2 NA18747.hp1 NA18946.hp2 others(14): Show |
intron_variant | MODIFIER | c.293-548_293-541del others(8): Show |
PAGE1 | ENSG00000068985.5 | transcript | ENST00000376150.4 | protein_coding | 4/5 | chrX | 49690083 | |||||||
chrX:49690088 | T | TAC | 5 | a0001c0001t0001g0002 a0001c0001t0001g0036 a0001c0001t0001g0039 others(2): Show |
6 | HG00733.hp2 HG03669.hp1 NA18978.hp2 others(3): Show |
intron_variant | MODIFIER | c.293-546_293-545ins others(2): Show |
PAGE1 | ENSG00000068985.5 | transcript | ENST00000376150.4 | protein_coding | 4/5 | chrX | 49690088 | |||||||
chrX:49690088 | T | TACACATA others(39): Show |
1 | a0001c0001t0001g0085 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.293-546_293-545ins others(46): Show |
PAGE1 | ENSG00000068985.5 | transcript | ENST00000376150.4 | protein_coding | 4/5 | chrX | 49690088 | |||||||
chrX:49690089 | G | A | 6 | a0001c0001t0001g0002 a0001c0001t0001g0036 a0001c0001t0001g0039 others(3): Show |
7 | HG00423.hp1 HG00733.hp2 HG03669.hp1 others(4): Show |
intron_variant | MODIFIER | c.293-546C>T | PAGE1 | ENSG00000068985.5 | transcript | ENST00000376150.4 | protein_coding | 4/5 | chrX | 49690089 | |||||||
chrX:49690090 | T | C | 6 | a0001c0001t0001g0002 a0001c0001t0001g0036 a0001c0001t0001g0039 others(3): Show |
7 | HG00423.hp1 HG00733.hp2 HG03669.hp1 others(4): Show |
intron_variant | MODIFIER | c.293-547A>G | PAGE1 | ENSG00000068985.5 | transcript | ENST00000376150.4 | protein_coding | 4/5 | chrX | 49690090 | |||||||
chrX:49690091 | G | A | 6 | a0001c0001t0001g0002 a0001c0001t0001g0036 a0001c0001t0001g0039 others(3): Show |
7 | HG00423.hp1 HG00733.hp2 HG03669.hp1 others(4): Show |
intron_variant | MODIFIER | c.293-548C>T | PAGE1 | ENSG00000068985.5 | transcript | ENST00000376150.4 | protein_coding | 4/5 | chrX | 49690091 | |||||||
chrX:49690091 | G | GTATATAT others(5): Show |
2 | a0001c0001t0001g0005 a0001c0001t0001g0007 |
2 | HG01258.hp1 NA18979.hp2 |
intron_variant | MODIFIER | c.293-549_293-548ins others(12): Show |
PAGE1 | ENSG00000068985.5 | transcript | ENST00000376150.4 | protein_coding | 4/5 | chrX | 49690091 | |||||||
chrX:49690091 | G | GTATATAT others(15): Show |
16 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(13): Show |
35 | HG01884.hp1 HG01891.hp1 HG01928.hp1 others(32): Show |
intron_variant | MODIFIER | c.293-570_293-549dup others(22): Show |
PAGE1 | ENSG00000068985.5 | transcript | ENST00000376150.4 | protein_coding | 4/5 | chrX | 49690091 | |||||||
chrX:49690091 | G | GTATATAT others(37): Show |
1 | a0001c0001t0001g0001 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.293-592_293-549dup others(44): Show |
PAGE1 | ENSG00000068985.5 | transcript | ENST00000376150.4 | protein_coding | 4/5 | chrX | 49690091 | |||||||
chrX:49690091 | GTATATAT others(15): Show |
G | 10 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0026 others(7): Show |
19 | HG00544.hp1 HG00558.hp1 HG00597.hp1 others(16): Show |
intron_variant | MODIFIER | c.293-570_293-549del others(22): Show |
PAGE1 | ENSG00000068985.5 | transcript | ENST00000376150.4 | protein_coding | 4/5 | chrX | 49690091 | |||||||
chrX:49690092 | TATATATG others(13): Show |
T | 3 | a0001c0001t0001g0054 a0001c0001t0001g0055 a0001c0001t0001g0056 |
3 | HG02451.hp1 HG02622.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.293-569_293-550del others(20): Show |
PAGE1 | ENSG00000068985.5 | transcript | ENST00000376150.4 | protein_coding | 4/5 | chrX | 49690092 | |||||||
chrX:49690098 | T | TAC | 3 | a0001c0001t0002g0018 a0001c0001t0002g0023 a0001c0001t0002g0040 |
6 | HG01081.hp1 HG02723.hp1 HG02976.hp1 others(3): Show |
intron_variant | MODIFIER | c.293-556_293-555ins others(2): Show |
PAGE1 | ENSG00000068985.5 | transcript | ENST00000376150.4 | protein_coding | 4/5 | chrX | 49690098 | |||||||
chrX:49690099 | G | A | 3 | a0001c0001t0002g0018 a0001c0001t0002g0023 a0001c0001t0002g0040 |
6 | HG01081.hp1 HG02723.hp1 HG02976.hp1 others(3): Show |
intron_variant | MODIFIER | c.293-556C>T | PAGE1 | ENSG00000068985.5 | transcript | ENST00000376150.4 | protein_coding | 4/5 | chrX | 49690099 | |||||||
chrX:49690100 | T | C | 3 | a0001c0001t0002g0018 a0001c0001t0002g0023 a0001c0001t0002g0040 |
6 | HG01081.hp1 HG02723.hp1 HG02976.hp1 others(3): Show |
intron_variant | MODIFIER | c.293-557A>G | PAGE1 | ENSG00000068985.5 | transcript | ENST00000376150.4 | protein_coding | 4/5 | chrX | 49690100 | |||||||
chrX:49690101 | G | A | 3 | a0001c0001t0002g0018 a0001c0001t0002g0023 a0001c0001t0002g0040 |
6 | HG01081.hp1 HG02723.hp1 HG02976.hp1 others(3): Show |
intron_variant | MODIFIER | c.293-558C>T | PAGE1 | ENSG00000068985.5 | transcript | ENST00000376150.4 | protein_coding | 4/5 | chrX | 49690101 | |||||||
chrX:49690102 | TATATATA others(3): Show |
T | 3 | a0001c0001t0001g0003 a0001c0001t0001g0047 a0001c0001t0001g0048 |
17 | HG01993.hp2 NA18747.hp1 NA18946.hp2 others(14): Show |
intron_variant | MODIFIER | c.293-569_293-560del others(10): Show |
PAGE1 | ENSG00000068985.5 | transcript | ENST00000376150.4 | protein_coding | 4/5 | chrX | 49690102 | |||||||
chrX:49690108 | T | C | 4 | a0001c0001t0001g0058 a0001c0001t0001g0059 a0001c0001t0001g0060 others(1): Show |
4 | HG02109.hp2 HG03195.hp1 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.293-565A>G | PAGE1 | ENSG00000068985.5 | transcript | ENST00000376150.4 | protein_coding | 4/5 | chrX | 49690108 | |||||||
chrX:49690109 | A | G | 3 | a0001c0001t0002g0018 a0001c0001t0002g0023 a0001c0001t0002g0040 |
6 | HG01081.hp1 HG02723.hp1 HG02976.hp1 others(3): Show |
intron_variant | MODIFIER | c.293-566T>C | PAGE1 | ENSG00000068985.5 | transcript | ENST00000376150.4 | protein_coding | 4/5 | chrX | 49690109 | |||||||
chrX:49690110 | C | T | 3 | a0001c0001t0002g0018 a0001c0001t0002g0023 a0001c0001t0002g0040 |
6 | HG01081.hp1 HG02723.hp1 HG02976.hp1 others(3): Show |
intron_variant | MODIFIER | c.293-567G>A | PAGE1 | ENSG00000068985.5 | transcript | ENST00000376150.4 | protein_coding | 4/5 | chrX | 49690110 | |||||||
chrX:49690111 | A | G | 3 | a0001c0001t0002g0018 a0001c0001t0002g0023 a0001c0001t0002g0040 |
6 | HG01081.hp1 HG02723.hp1 HG02976.hp1 others(3): Show |
intron_variant | MODIFIER | c.293-568T>C | PAGE1 | ENSG00000068985.5 | transcript | ENST00000376150.4 | protein_coding | 4/5 | chrX | 49690111 | |||||||
chrX:49690112 | C | T | 3 | a0001c0001t0002g0018 a0001c0001t0002g0023 a0001c0001t0002g0040 |
6 | HG01081.hp1 HG02723.hp1 HG02976.hp1 others(3): Show |
intron_variant | MODIFIER | c.293-569G>A | PAGE1 | ENSG00000068985.5 | transcript | ENST00000376150.4 | protein_coding | 4/5 | chrX | 49690112 | |||||||
chrX:49690113 | A | ATATATAT others(3): Show |
2 | a0001c0001t0001g0060 a0001c0001t0001g0091 |
2 | HG03471.hp1 NA18947.hp2 |
intron_variant | MODIFIER | c.293-580_293-571dup others(10): Show |
PAGE1 | ENSG00000068985.5 | transcript | ENST00000376150.4 | protein_coding | 4/5 | chrX | 49690113 | |||||||
chrX:49690113 | A | ATATATAT others(13): Show |
2 | a0001c0001t0001g0058 a0001c0001t0001g0059 |
2 | HG02109.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.293-571_293-570ins others(20): Show |
PAGE1 | ENSG00000068985.5 | transcript | ENST00000376150.4 | protein_coding | 4/5 | chrX | 49690113 | |||||||
chrX:49690123 | GTA | G | 4 | a0002c0002t0001g0049 a0002c0002t0001g0050 a0002c0002t0001g0052 others(1): Show |
4 | HG02965.hp1 HG03041.hp2 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.293-582_293-581del others(2): Show |
PAGE1 | ENSG00000068985.5 | transcript | ENST00000376150.4 | protein_coding | 4/5 | chrX | 49690123 | |||||||
chrX:49690123 | GTATATAT others(5): Show |
G | 1 | a0001c0001t0001g0082 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.293-592_293-581del others(12): Show |
PAGE1 | ENSG00000068985.5 | transcript | ENST00000376150.4 | protein_coding | 4/5 | chrX | 49690123 | |||||||
chrX:49690135 | A | G | 2 | a0001c0001t0001g0028 a0001c0001t0001g0063 |
3 | HG02257.hp1 HG02630.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.293-592T>C | PAGE1 | ENSG00000068985.5 | transcript | ENST00000376150.4 | protein_coding | 4/5 | chrX | 49690135 | |||||||
chrX:49690143 | G | T | 1 | a0001c0001t0001g0055 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.293-600C>A | PAGE1 | ENSG00000068985.5 | transcript | ENST00000376150.4 | protein_coding | 4/5 | chrX | 49690143 | |||||||
chrX:49690671 | A | G | 7 | a0001c0001t0001g0054 a0001c0001t0001g0055 a0001c0001t0001g0056 others(4): Show |
11 | HG01081.hp1 HG02055.hp1 HG02451.hp1 others(8): Show |
intron_variant | MODIFIER | c.292+578T>C | PAGE1 | ENSG00000068985.5 | transcript | ENST00000376150.4 | protein_coding | 4/5 | chrX | 49690671 | |||||||
chrX:49690709 | T | A | 1 | a0001c0001t0001g0109 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.292+540A>T | PAGE1 | ENSG00000068985.5 | transcript | ENST00000376150.4 | protein_coding | 4/5 | chrX | 49690709 | |||||||
chrX:49690854 | G | A | 1 | a0001c0001t0001g0110 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.292+395C>T | PAGE1 | ENSG00000068985.5 | transcript | ENST00000376150.4 | protein_coding | 4/5 | chrX | 49690854 | |||||||
chrX:49690869 | CA | C | 16 | a0001c0001t0001g0003 a0001c0001t0001g0046 a0001c0001t0001g0047 others(13): Show |
30 | HG01934.hp1 HG01993.hp2 HG02132.hp1 others(27): Show |
intron_variant | MODIFIER | c.292+379delT | PAGE1 | ENSG00000068985.5 | transcript | ENST00000376150.4 | protein_coding | 4/5 | chrX | 49690869 | |||||||
chrX:49691750 | T | C | 1 | a0001c0001t0001g0056 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.167-376A>G | PAGE1 | ENSG00000068985.5 | transcript | ENST00000376150.4 | protein_coding | 3/5 | chrX | 49691750 | |||||||
chrX:49691811 | G | A | 1 | a0004c0007t0001g0125 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.167-437C>T | PAGE1 | ENSG00000068985.5 | transcript | ENST00000376150.4 | protein_coding | 3/5 | chrX | 49691811 | |||||||
chrX:49691849 | T | A | 1 | a0001c0001t0001g0091 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.167-475A>T | PAGE1 | ENSG00000068985.5 | transcript | ENST00000376150.4 | protein_coding | 3/5 | chrX | 49691849 | |||||||
chrX:49691862 | C | T | 1 | a0001c0001t0001g0078 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.167-488G>A | PAGE1 | ENSG00000068985.5 | transcript | ENST00000376150.4 | protein_coding | 3/5 | chrX | 49691862 | |||||||
chrX:49692009 | C | T | 1 | a0001c0001t0001g0077 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.167-635G>A | PAGE1 | ENSG00000068985.5 | transcript | ENST00000376150.4 | protein_coding | 3/5 | chrX | 49692009 | |||||||
chrX:49692123 | G | A | 3 | a0001c0001t0001g0054 a0001c0001t0001g0055 a0001c0001t0001g0056 |
3 | HG02451.hp1 HG02622.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.167-749C>T | PAGE1 | ENSG00000068985.5 | transcript | ENST00000376150.4 | protein_coding | 3/5 | chrX | 49692123 | |||||||
chrX:49692146 | GA | G | 15 | a0001c0001t0001g0003 a0001c0001t0001g0046 a0001c0001t0001g0047 others(12): Show |
33 | HG01081.hp1 HG01993.hp2 HG02055.hp1 others(30): Show |
intron_variant | MODIFIER | c.167-773delT | PAGE1 | ENSG00000068985.5 | transcript | ENST00000376150.4 | protein_coding | 3/5 | chrX | 49692146 | |||||||
chrX:49692214 | G | A | 16 | a0001c0001t0001g0003 a0001c0001t0001g0046 a0001c0001t0001g0047 others(13): Show |
34 | HG01081.hp1 HG01993.hp2 HG02055.hp1 others(31): Show |
intron_variant | MODIFIER | c.167-840C>T | PAGE1 | ENSG00000068985.5 | transcript | ENST00000376150.4 | protein_coding | 3/5 | chrX | 49692214 | |||||||
chrX:49692403 | G | A | 1 | a0001c0001t0001g0067 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.167-1029C>T | PAGE1 | ENSG00000068985.5 | transcript | ENST00000376150.4 | protein_coding | 3/5 | chrX | 49692403 | |||||||
chrX:49692456 | C | T | 16 | a0001c0001t0001g0003 a0001c0001t0001g0046 a0001c0001t0001g0047 others(13): Show |
34 | HG01081.hp1 HG01993.hp2 HG02055.hp1 others(31): Show |
intron_variant | MODIFIER | c.167-1082G>A | PAGE1 | ENSG00000068985.5 | transcript | ENST00000376150.4 | protein_coding | 3/5 | chrX | 49692456 | |||||||
chrX:49692568 | T | C | 2 | a0001c0001t0001g0066 a0001c0001t0001g0067 |
2 | HG02886.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.167-1194A>G | PAGE1 | ENSG00000068985.5 | transcript | ENST00000376150.4 | protein_coding | 3/5 | chrX | 49692568 | |||||||
chrX:49692622 | C | G | 7 | a0001c0001t0001g0010 a0001c0001t0001g0019 a0001c0001t0001g0069 others(4): Show |
14 | HG00621.hp1 HG02293.hp1 NA18942.hp2 others(11): Show |
intron_variant | MODIFIER | c.167-1248G>C | PAGE1 | ENSG00000068985.5 | transcript | ENST00000376150.4 | protein_coding | 3/5 | chrX | 49692622 | |||||||
chrX:49692627 | G | GTT | 4 | a0001c0001t0001g0003 a0001c0001t0001g0046 a0001c0001t0001g0047 others(1): Show |
18 | HG01993.hp2 HG02132.hp1 NA18747.hp1 others(15): Show |
intron_variant | MODIFIER | c.167-1255_167-1254d others(4): Show |
PAGE1 | ENSG00000068985.5 | transcript | ENST00000376150.4 | protein_coding | 3/5 | chrX | 49692627 | |||||||
chrX:49692744 | A | G | 9 | a0001c0001t0001g0003 a0001c0001t0001g0046 a0001c0001t0001g0047 others(6): Show |
23 | HG01993.hp2 HG02132.hp1 HG02622.hp2 others(20): Show |
intron_variant | MODIFIER | c.166+1355T>C | PAGE1 | ENSG00000068985.5 | transcript | ENST00000376150.4 | protein_coding | 3/5 | chrX | 49692744 | |||||||
chrX:49692753 | A | G | 1 | a0001c0001t0001g0075 | 1 | NA19078.hp1 | intron_variant | MODIFIER | c.166+1346T>C | PAGE1 | ENSG00000068985.5 | transcript | ENST00000376150.4 | protein_coding | 3/5 | chrX | 49692753 | |||||||
chrX:49692783 | A | ATTATTTA others(1): Show |
11 | a0001c0001t0001g0054 a0001c0001t0001g0055 a0001c0001t0001g0056 others(8): Show |
15 | HG01081.hp1 HG02055.hp1 HG02451.hp1 others(12): Show |
intron_variant | MODIFIER | c.166+1308_166+1315d others(10): Show |
PAGE1 | ENSG00000068985.5 | transcript | ENST00000376150.4 | protein_coding | 3/5 | chrX | 49692783 | |||||||
chrX:49692783 | A | ATTATTTA others(5): Show |
1 | a0002c0002t0001g0050 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.166+1304_166+1315d others(14): Show |
PAGE1 | ENSG00000068985.5 | transcript | ENST00000376150.4 | protein_coding | 3/5 | chrX | 49692783 | |||||||
chrX:49692783 | A | ATTATTTA others(9): Show |
4 | a0001c0001t0001g0003 a0001c0001t0001g0046 a0001c0001t0001g0047 others(1): Show |
18 | HG01993.hp2 HG02132.hp1 NA18747.hp1 others(15): Show |
intron_variant | MODIFIER | c.166+1300_166+1315d others(18): Show |
PAGE1 | ENSG00000068985.5 | transcript | ENST00000376150.4 | protein_coding | 3/5 | chrX | 49692783 | |||||||
chrX:49692869 | C | T | 1 | a0001c0001t0001g0068 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.166+1230G>A | PAGE1 | ENSG00000068985.5 | transcript | ENST00000376150.4 | protein_coding | 3/5 | chrX | 49692869 | |||||||
chrX:49692901 | T | G | 9 | a0001c0001t0001g0003 a0001c0001t0001g0046 a0001c0001t0001g0047 others(6): Show |
23 | HG01993.hp2 HG02132.hp1 HG02622.hp2 others(20): Show |
intron_variant | MODIFIER | c.166+1198A>C | PAGE1 | ENSG00000068985.5 | transcript | ENST00000376150.4 | protein_coding | 3/5 | chrX | 49692901 | |||||||
chrX:49693005 | A | C | 4 | a0001c0001t0002g0018 a0001c0001t0002g0023 a0001c0001t0002g0024 others(1): Show |
8 | HG01081.hp1 HG02055.hp1 HG02723.hp1 others(5): Show |
intron_variant | MODIFIER | c.166+1094T>G | PAGE1 | ENSG00000068985.5 | transcript | ENST00000376150.4 | protein_coding | 3/5 | chrX | 49693005 | |||||||
chrX:49693041 | T | C | 1 | a0001c0001t0001g0074 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.166+1058A>G | PAGE1 | ENSG00000068985.5 | transcript | ENST00000376150.4 | protein_coding | 3/5 | chrX | 49693041 | |||||||
chrX:49693078 | T | C | 4 | a0001c0001t0002g0018 a0001c0001t0002g0023 a0001c0001t0002g0024 others(1): Show |
8 | HG01081.hp1 HG02055.hp1 HG02723.hp1 others(5): Show |
intron_variant | MODIFIER | c.166+1021A>G | PAGE1 | ENSG00000068985.5 | transcript | ENST00000376150.4 | protein_coding | 3/5 | chrX | 49693078 | |||||||
chrX:49693316 | G | A | 7 | a0001c0001t0001g0054 a0001c0001t0001g0055 a0001c0001t0001g0056 others(4): Show |
11 | HG01081.hp1 HG02055.hp1 HG02451.hp1 others(8): Show |
intron_variant | MODIFIER | c.166+783C>T | PAGE1 | ENSG00000068985.5 | transcript | ENST00000376150.4 | protein_coding | 3/5 | chrX | 49693316 | |||||||
chrX:49693555 | T | C | 1 | a0001c0001t0001g0091 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.166+544A>G | PAGE1 | ENSG00000068985.5 | transcript | ENST00000376150.4 | protein_coding | 3/5 | chrX | 49693555 | |||||||
chrX:49693637 | G | C | 16 | a0001c0001t0001g0003 a0001c0001t0001g0046 a0001c0001t0001g0047 others(13): Show |
34 | HG01081.hp1 HG01993.hp2 HG02055.hp1 others(31): Show |
intron_variant | MODIFIER | c.166+462C>G | PAGE1 | ENSG00000068985.5 | transcript | ENST00000376150.4 | protein_coding | 3/5 | chrX | 49693637 | |||||||
chrX:49693785 | C | A | 9 | a0001c0001t0001g0003 a0001c0001t0001g0046 a0001c0001t0001g0047 others(6): Show |
23 | HG01993.hp2 HG02132.hp1 HG02622.hp2 others(20): Show |
intron_variant | MODIFIER | c.166+314G>T | PAGE1 | ENSG00000068985.5 | transcript | ENST00000376150.4 | protein_coding | 3/5 | chrX | 49693785 | |||||||
chrX:49693787 | C | G | 3 | a0001c0001t0001g0054 a0001c0001t0001g0055 a0001c0001t0001g0056 |
3 | HG02451.hp1 HG02622.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.166+312G>C | PAGE1 | ENSG00000068985.5 | transcript | ENST00000376150.4 | protein_coding | 3/5 | chrX | 49693787 | |||||||
chrX:49693830 | T | C | 4 | a0001c0001t0001g0003 a0001c0001t0001g0046 a0001c0001t0001g0047 others(1): Show |
18 | HG01993.hp2 HG02132.hp1 NA18747.hp1 others(15): Show |
intron_variant | MODIFIER | c.166+269A>G | PAGE1 | ENSG00000068985.5 | transcript | ENST00000376150.4 | protein_coding | 3/5 | chrX | 49693830 | |||||||
chrX:49693918 | A | G | 1 | a0001c0001t0001g0043 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.166+181T>C | PAGE1 | ENSG00000068985.5 | transcript | ENST00000376150.4 | protein_coding | 3/5 | chrX | 49693918 | |||||||
chrX:49693960 | T | C | 1 | a0001c0001t0001g0120 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.166+139A>G | PAGE1 | ENSG00000068985.5 | transcript | ENST00000376150.4 | protein_coding | 3/5 | chrX | 49693960 | |||||||
chrX:49693995 | T | A | 7 | a0001c0001t0001g0054 a0001c0001t0001g0055 a0001c0001t0001g0056 others(4): Show |
11 | HG01081.hp1 HG02055.hp1 HG02451.hp1 others(8): Show |
intron_variant | MODIFIER | c.166+104A>T | PAGE1 | ENSG00000068985.5 | transcript | ENST00000376150.4 | protein_coding | 3/5 | chrX | 49693995 | |||||||
chrX:49694021 | G | GAC | 15 | a0001c0001t0001g0005 a0001c0001t0001g0010 a0001c0001t0001g0025 others(12): Show |
29 | HG00099.hp2 HG00408.hp2 HG01168.hp1 others(26): Show |
intron_variant | MODIFIER | c.166+76_166+77dupGT | PAGE1 | ENSG00000068985.5 | transcript | ENST00000376150.4 | protein_coding | 3/5 | chrX | 49694021 | |||||||
chrX:49694021 | G | GACAC | 14 | a0001c0001t0001g0004 a0001c0001t0001g0011 a0001c0001t0001g0037 others(11): Show |
32 | HG00099.hp1 HG00280.hp1 HG00438.hp1 others(29): Show |
intron_variant | MODIFIER | c.166+74_166+77dupGT others(2): Show |
PAGE1 | ENSG00000068985.5 | transcript | ENST00000376150.4 | protein_coding | 3/5 | chrX | 49694021 | |||||||
chrX:49694021 | G | GACACAC | 9 | a0001c0001t0001g0002 a0001c0001t0001g0039 a0001c0001t0001g0111 others(6): Show |
27 | HG00438.hp2 HG00597.hp2 HG00639.hp2 others(24): Show |
intron_variant | MODIFIER | c.166+72_166+77dupGT others(4): Show |
PAGE1 | ENSG00000068985.5 | transcript | ENST00000376150.4 | protein_coding | 3/5 | chrX | 49694021 | |||||||
chrX:49694021 | G | GACACACA others(1): Show |
3 | a0001c0001t0001g0117 a0001c0001t0001g0118 a0001c0001t0001g0119 |
3 | HG00544.hp1 NA19005.hp1 NA19062.hp1 |
intron_variant | MODIFIER | c.166+70_166+77dupGT others(6): Show |
PAGE1 | ENSG00000068985.5 | transcript | ENST00000376150.4 | protein_coding | 3/5 | chrX | 49694021 | |||||||
chrX:49694021 | GAC | G | 15 | a0001c0001t0001g0003 a0001c0001t0001g0013 a0001c0001t0001g0027 others(12): Show |
35 | HG00323.hp1 HG00639.hp1 HG00735.hp1 others(32): Show |
intron_variant | MODIFIER | c.166+76_166+77delGT | PAGE1 | ENSG00000068985.5 | transcript | ENST00000376150.4 | protein_coding | 3/5 | chrX | 49694021 | |||||||
chrX:49694021 | GACAC | G | 13 | a0001c0001t0001g0008 a0001c0001t0001g0026 a0001c0001t0001g0028 others(10): Show |
20 | HG00323.hp2 HG02109.hp1 HG02109.hp2 others(17): Show |
intron_variant | MODIFIER | c.166+74_166+77delGT others(2): Show |
PAGE1 | ENSG00000068985.5 | transcript | ENST00000376150.4 | protein_coding | 3/5 | chrX | 49694021 | |||||||
chrX:49694021 | GACACAC | G | 8 | a0001c0001t0001g0043 a0001c0001t0001g0055 a0001c0001t0001g0056 others(5): Show |
12 | HG00738.hp1 HG01081.hp1 HG02055.hp1 others(9): Show |
intron_variant | MODIFIER | c.166+72_166+77delGT others(4): Show |
PAGE1 | ENSG00000068985.5 | transcript | ENST00000376150.4 | protein_coding | 3/5 | chrX | 49694021 | |||||||
chrX:49694021 | GACACACA others(1): Show |
G | 2 | a0001c0001t0001g0054 a0001c0001t0003g0017 |
5 | HG02622.hp1 HG02896.hp1 HG02897.hp2 others(2): Show |
intron_variant | MODIFIER | c.166+70_166+77delGT others(6): Show |
PAGE1 | ENSG00000068985.5 | transcript | ENST00000376150.4 | protein_coding | 3/5 | chrX | 49694021 | |||||||
chrX:49694064 | A | C | 1 | a0001c0001t0001g0001 | 3 | HG02040.hp1 NA18939.hp2 NA19055.hp1 |
intron_variant | MODIFIER | c.166+35T>G | PAGE1 | ENSG00000068985.5 | transcript | ENST00000376150.4 | protein_coding | 3/5 | chrX | 49694064 | |||||||
chrX:49694065 | C | CACA | 3 | a0001c0001t0001g0014 a0001c0001t0001g0016 a0001c0001t0001g0122 |
4 | HG00544.hp2 HG02080.hp2 HG03834.hp1 others(1): Show |
intron_variant | MODIFIER | c.166+33_166+34insTG others(1): Show |
PAGE1 | ENSG00000068985.5 | transcript | ENST00000376150.4 | protein_coding | 3/5 | chrX | 49694065 | |||||||
chrX:49694066 | C | A | 2 | a0001c0001t0001g0120 a0001c0001t0001g0121 |
2 | HG00408.hp2 NA18956.hp2 |
intron_variant | MODIFIER | c.166+33G>T | PAGE1 | ENSG00000068985.5 | transcript | ENST00000376150.4 | protein_coding | 3/5 | chrX | 49694066 | |||||||
chrX:49694067 | C | A | 1 | a0001c0001t0001g0122 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.166+32G>T | PAGE1 | ENSG00000068985.5 | transcript | ENST00000376150.4 | protein_coding | 3/5 | chrX | 49694067 | |||||||
chrX:49694261 | T | A | 3 | a0001c0001t0001g0058 a0001c0001t0001g0059 a0001c0001t0001g0060 |
3 | HG02109.hp2 HG03195.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.64-60A>T | PAGE1 | ENSG00000068985.5 | transcript | ENST00000376150.4 | protein_coding | 2/5 | chrX | 49694261 | |||||||
chrX:49694391 | C | T | 1 | a0001c0001t0001g0061 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.64-190G>A | PAGE1 | ENSG00000068985.5 | transcript | ENST00000376150.4 | protein_coding | 2/5 | chrX | 49694391 | |||||||
chrX:49694521 | GA | G | 3 | a0001c0001t0002g0018 a0001c0001t0002g0023 a0001c0001t0002g0040 |
6 | HG01081.hp1 HG02723.hp1 HG02976.hp1 others(3): Show |
intron_variant | MODIFIER | c.63+186delT | PAGE1 | ENSG00000068985.5 | transcript | ENST00000376150.4 | protein_coding | 2/5 | chrX | 49694521 | |||||||
chrX:49694555 | C | G | 4 | a0001c0001t0001g0003 a0001c0001t0001g0046 a0001c0001t0001g0047 others(1): Show |
18 | HG01993.hp2 HG02132.hp1 NA18747.hp1 others(15): Show |
intron_variant | MODIFIER | c.63+153G>C | PAGE1 | ENSG00000068985.5 | transcript | ENST00000376150.4 | protein_coding | 2/5 | chrX | 49694555 | |||||||
chrX:49694563 | A | G | 24 | a0001c0001t0001g0003 a0001c0001t0001g0026 a0001c0001t0001g0027 others(21): Show |
47 | HG00738.hp1 HG01081.hp1 HG01993.hp2 others(44): Show |
intron_variant | MODIFIER | c.63+145T>C | PAGE1 | ENSG00000068985.5 | transcript | ENST00000376150.4 | protein_coding | 2/5 | chrX | 49694563 | |||||||
chrX:49694574 | A | AT | 9 | a0001c0001t0001g0003 a0001c0001t0001g0046 a0001c0001t0001g0047 others(6): Show |
23 | HG01993.hp2 HG02132.hp1 HG02622.hp2 others(20): Show |
intron_variant | MODIFIER | c.63+133dupA | PAGE1 | ENSG00000068985.5 | transcript | ENST00000376150.4 | protein_coding | 2/5 | chrX | 49694574 | |||||||
chrX:49694591 | G | T | 1 | a0001c0001t0001g0025 | 2 | NA18956.hp1 NA18967.hp1 |
intron_variant | MODIFIER | c.63+117C>A | PAGE1 | ENSG00000068985.5 | transcript | ENST00000376150.4 | protein_coding | 2/5 | chrX | 49694591 | |||||||
chrX:49694593 | A | G | 1 | a0001c0001t0001g0045 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.63+115T>C | PAGE1 | ENSG00000068985.5 | transcript | ENST00000376150.4 | protein_coding | 2/5 | chrX | 49694593 | |||||||
chrX:49695052 | C | T | 1 | a0001c0001t0001g0043 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.-8-274G>A | PAGE1 | ENSG00000068985.5 | transcript | ENST00000376150.4 | protein_coding | 1/5 | chrX | 49695052 | |||||||
chrX:49695149 | C | T | 1 | a0001c0001t0001g0042 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.-8-371G>A | PAGE1 | ENSG00000068985.5 | transcript | ENST00000376150.4 | protein_coding | 1/5 | chrX | 49695149 | |||||||
chrX:49695680 | A | G | 1 | a0001c0001t0001g0041 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.-9+189T>C | PAGE1 | ENSG00000068985.5 | transcript | ENST00000376150.4 | protein_coding | 1/5 | chrX | 49695680 |