Item | Value |
---|---|
geneid | 416 |
ensemblid | ENSG00000062096.15 |
hgncid | 721 |
symbol | ARSF |
name | arylsulfatase F |
refseq_nuc | NM_001201539.2 |
refseq_prot | NP_001188468.1 |
ensembl_nuc | ENST00000381127.6 |
ensembl_prot | ENSP00000370519.1 |
mane_status | MANE Select |
chr | chrX |
start | 3041471 |
end | 3112727 |
strand | + |
ver | v1.2 |
region | chrX:3041471-3112727 |
region5000 | chrX:3036471-3117727 |
regionname0 | ARSF_chrX_3041471_3112727 |
regionname5000 | ARSF_chrX_3036471_3117727 |
ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 1/1 | 590 | 170 | 32 | 25 | 75 | 10 | 26 | 61 | ARSF_chrX_3036471_3117727 | ARSF | MRPRR others(585): Show |
chrX | 3036471 | 3117727 |
a0002 | 0/0 | 590 | 9 | 2 | 5 | 1 | 1 | 0 | 0 | ARSF_chrX_3036471_3117727 | ARSF | MRPRR others(585): Show |
chrX | 3036471 | 3117727 |
a0003 | 0/0 | 590 | 4 | 3 | 1 | 0 | 0 | 0 | 0 | ARSF_chrX_3036471_3117727 | ARSF | MRPRR others(585): Show |
chrX | 3036471 | 3117727 |
a0004 | 0/0 | 590 | 3 | 1 | 2 | 0 | 0 | 0 | 0 | ARSF_chrX_3036471_3117727 | ARSF | MRPRR others(585): Show |
chrX | 3036471 | 3117727 |
a0005 | 0/0 | 590 | 3 | 3 | 0 | 0 | 0 | 0 | 0 | ARSF_chrX_3036471_3117727 | ARSF | MRPRR others(585): Show |
chrX | 3036471 | 3117727 |
a0006 | 0/0 | 584 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | ARSF_chrX_3036471_3117727 | ARSF | MRPRR others(579): Show |
chrX | 3036471 | 3117727 |
a0007 | 0/0 | 590 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | ARSF_chrX_3036471_3117727 | ARSF | MRPRR others(585): Show |
chrX | 3036471 | 3117727 |
a0008 | 0/0 | 590 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | ARSF_chrX_3036471_3117727 | ARSF | MRPRR others(585): Show |
chrX | 3036471 | 3117727 |
achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 0/0 | 1770 | 141 | 18 | 21 | 74 | 8 | 20 | ARSF_chrX_3036471_3117727 | ARSF | ATGAG others(1765): Show |
chrX | 3036471 | 3117727 | ||
a0001c0002 | 1/1 | 1770 | 15 | 4 | 4 | 1 | 2 | 2 | ARSF_chrX_3036471_3117727 | ARSF | ATGAG others(1765): Show |
chrX | 3036471 | 3117727 | ||
a0001c0005 | 0/0 | 1770 | 4 | 4 | 0 | 0 | 0 | 0 | ARSF_chrX_3036471_3117727 | ARSF | ATGAG others(1765): Show |
chrX | 3036471 | 3117727 | ||
a0001c0007 | 0/0 | 1770 | 2 | 2 | 0 | 0 | 0 | 0 | ARSF_chrX_3036471_3117727 | ARSF | ATGAG others(1765): Show |
chrX | 3036471 | 3117727 | ||
a0001c0009 | 0/0 | 1820 | 2 | 0 | 0 | 0 | 0 | 2 | ARSF_chrX_3036471_3117727 | ARSF | ATGAG others(1815): Show |
chrX | 3036471 | 3117727 | ||
a0001c0010 | 0/0 | 1770 | 2 | 2 | 0 | 0 | 0 | 0 | ARSF_chrX_3036471_3117727 | ARSF | ATGAG others(1765): Show |
chrX | 3036471 | 3117727 | ||
a0001c0012 | 0/0 | 1770 | 1 | 1 | 0 | 0 | 0 | 0 | ARSF_chrX_3036471_3117727 | ARSF | ATGAG others(1765): Show |
chrX | 3036471 | 3117727 | ||
a0001c0015 | 0/0 | 1770 | 1 | 0 | 0 | 0 | 0 | 1 | ARSF_chrX_3036471_3117727 | ARSF | ATGAG others(1765): Show |
chrX | 3036471 | 3117727 | ||
a0001c0016 | 0/0 | 1770 | 1 | 1 | 0 | 0 | 0 | 0 | ARSF_chrX_3036471_3117727 | ARSF | ATGAG others(1765): Show |
chrX | 3036471 | 3117727 | ||
a0001c0019 | 0/0 | 1770 | 1 | 0 | 0 | 0 | 0 | 1 | ARSF_chrX_3036471_3117727 | ARSF | ATGAG others(1765): Show |
chrX | 3036471 | 3117727 | ||
a0002c0003 | 0/0 | 1770 | 5 | 1 | 3 | 1 | 0 | 0 | ARSF_chrX_3036471_3117727 | ARSF | ATGAG others(1765): Show |
chrX | 3036471 | 3117727 | ||
a0002c0004 | 0/0 | 1770 | 4 | 1 | 2 | 0 | 1 | 0 | ARSF_chrX_3036471_3117727 | ARSF | ATGAG others(1765): Show |
chrX | 3036471 | 3117727 | ||
a0003c0008 | 0/0 | 1770 | 2 | 2 | 0 | 0 | 0 | 0 | ARSF_chrX_3036471_3117727 | ARSF | ATGAG others(1765): Show |
chrX | 3036471 | 3117727 | ||
a0003c0013 | 0/0 | 1770 | 1 | 1 | 0 | 0 | 0 | 0 | ARSF_chrX_3036471_3117727 | ARSF | ATGAG others(1765): Show |
chrX | 3036471 | 3117727 | ||
a0003c0017 | 0/0 | 1770 | 1 | 0 | 1 | 0 | 0 | 0 | ARSF_chrX_3036471_3117727 | ARSF | ATGAG others(1765): Show |
chrX | 3036471 | 3117727 | ||
a0004c0006 | 0/0 | 1770 | 3 | 1 | 2 | 0 | 0 | 0 | ARSF_chrX_3036471_3117727 | ARSF | ATGAG others(1765): Show |
chrX | 3036471 | 3117727 | ||
a0005c0011 | 0/0 | 1770 | 2 | 2 | 0 | 0 | 0 | 0 | ARSF_chrX_3036471_3117727 | ARSF | ATGAG others(1765): Show |
chrX | 3036471 | 3117727 | ||
a0005c0022 | 0/0 | 1770 | 1 | 1 | 0 | 0 | 0 | 0 | ARSF_chrX_3036471_3117727 | ARSF | ATGAG others(1765): Show |
chrX | 3036471 | 3117727 | ||
a0006c0014 | 0/0 | 1752 | 1 | 1 | 0 | 0 | 0 | 0 | ARSF_chrX_3036471_3117727 | ARSF | ATGAG others(1747): Show |
chrX | 3036471 | 3117727 | ||
a0006c0018 | 0/0 | 1752 | 1 | 1 | 0 | 0 | 0 | 0 | ARSF_chrX_3036471_3117727 | ARSF | ATGAG others(1747): Show |
chrX | 3036471 | 3117727 | ||
a0007c0021 | 0/0 | 1770 | 1 | 0 | 0 | 1 | 0 | 0 | ARSF_chrX_3036471_3117727 | ARSF | ATGAG others(1765): Show |
chrX | 3036471 | 3117727 | ||
a0008c0020 | 0/0 | 1770 | 1 | 0 | 0 | 1 | 0 | 0 | ARSF_chrX_3036471_3117727 | ARSF | ATGAG others(1765): Show |
chrX | 3036471 | 3117727 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 0/0 | 2165 | 139 | 18 | 21 | 72 | 8 | 20 | ARSF_chrX_3036471_3117727 | ARSF | AGTGG others(2160): Show |
chrX | 3036471 | 3117727 |
a0001c0001t0004 | 0/0 | 2165 | 1 | 0 | 0 | 1 | 0 | 0 | ARSF_chrX_3036471_3117727 | ARSF | AGTGG others(2160): Show |
chrX | 3036471 | 3117727 |
a0001c0001t0005 | 0/0 | 2165 | 1 | 0 | 0 | 1 | 0 | 0 | ARSF_chrX_3036471_3117727 | ARSF | AGTGG others(2160): Show |
chrX | 3036471 | 3117727 |
a0001c0002t0001 | 1/1 | 2165 | 15 | 4 | 4 | 1 | 2 | 2 | ARSF_chrX_3036471_3117727 | ARSF | AGTGG others(2160): Show |
chrX | 3036471 | 3117727 |
a0001c0005t0001 | 0/0 | 2165 | 4 | 4 | 0 | 0 | 0 | 0 | ARSF_chrX_3036471_3117727 | ARSF | AGTGG others(2160): Show |
chrX | 3036471 | 3117727 |
a0001c0007t0003 | 0/0 | 2165 | 2 | 2 | 0 | 0 | 0 | 0 | ARSF_chrX_3036471_3117727 | ARSF | AGTGG others(2160): Show |
chrX | 3036471 | 3117727 |
a0001c0009t0001 | 0/0 | 2215 | 2 | 0 | 0 | 0 | 0 | 2 | ARSF_chrX_3036471_3117727 | ARSF | AGTGG others(2210): Show |
chrX | 3036471 | 3117727 |
a0001c0010t0001 | 0/0 | 2165 | 2 | 2 | 0 | 0 | 0 | 0 | ARSF_chrX_3036471_3117727 | ARSF | AGTGG others(2160): Show |
chrX | 3036471 | 3117727 |
a0001c0012t0001 | 0/0 | 2165 | 1 | 1 | 0 | 0 | 0 | 0 | ARSF_chrX_3036471_3117727 | ARSF | AGTGG others(2160): Show |
chrX | 3036471 | 3117727 |
a0001c0015t0006 | 0/0 | 2215 | 1 | 0 | 0 | 0 | 0 | 1 | ARSF_chrX_3036471_3117727 | ARSF | AGTGG others(2210): Show |
chrX | 3036471 | 3117727 |
a0001c0016t0001 | 0/0 | 2165 | 1 | 1 | 0 | 0 | 0 | 0 | ARSF_chrX_3036471_3117727 | ARSF | AGTGG others(2160): Show |
chrX | 3036471 | 3117727 |
a0001c0019t0001 | 0/0 | 2165 | 1 | 0 | 0 | 0 | 0 | 1 | ARSF_chrX_3036471_3117727 | ARSF | AGTGG others(2160): Show |
chrX | 3036471 | 3117727 |
a0002c0003t0001 | 0/0 | 2165 | 5 | 1 | 3 | 1 | 0 | 0 | ARSF_chrX_3036471_3117727 | ARSF | AGTGG others(2160): Show |
chrX | 3036471 | 3117727 |
a0002c0004t0001 | 0/0 | 2165 | 4 | 1 | 2 | 0 | 1 | 0 | ARSF_chrX_3036471_3117727 | ARSF | AGTGG others(2160): Show |
chrX | 3036471 | 3117727 |
a0003c0008t0001 | 0/0 | 2165 | 2 | 2 | 0 | 0 | 0 | 0 | ARSF_chrX_3036471_3117727 | ARSF | AGTGG others(2160): Show |
chrX | 3036471 | 3117727 |
a0003c0013t0001 | 0/0 | 2165 | 1 | 1 | 0 | 0 | 0 | 0 | ARSF_chrX_3036471_3117727 | ARSF | AGTGG others(2160): Show |
chrX | 3036471 | 3117727 |
a0003c0017t0001 | 0/0 | 2165 | 1 | 0 | 1 | 0 | 0 | 0 | ARSF_chrX_3036471_3117727 | ARSF | AGTGG others(2160): Show |
chrX | 3036471 | 3117727 |
a0004c0006t0001 | 0/0 | 2165 | 3 | 1 | 2 | 0 | 0 | 0 | ARSF_chrX_3036471_3117727 | ARSF | AGTGG others(2160): Show |
chrX | 3036471 | 3117727 |
a0005c0011t0001 | 0/0 | 2165 | 2 | 2 | 0 | 0 | 0 | 0 | ARSF_chrX_3036471_3117727 | ARSF | AGTGG others(2160): Show |
chrX | 3036471 | 3117727 |
a0005c0022t0001 | 0/0 | 2165 | 1 | 1 | 0 | 0 | 0 | 0 | ARSF_chrX_3036471_3117727 | ARSF | AGTGG others(2160): Show |
chrX | 3036471 | 3117727 |
a0006c0014t0002 | 0/0 | 2115 | 1 | 1 | 0 | 0 | 0 | 0 | ARSF_chrX_3036471_3117727 | ARSF | AGTGG others(2110): Show |
chrX | 3036471 | 3117727 |
a0006c0018t0002 | 0/0 | 2115 | 1 | 1 | 0 | 0 | 0 | 0 | ARSF_chrX_3036471_3117727 | ARSF | AGTGG others(2110): Show |
chrX | 3036471 | 3117727 |
a0007c0021t0001 | 0/0 | 2165 | 1 | 0 | 0 | 1 | 0 | 0 | ARSF_chrX_3036471_3117727 | ARSF | AGTGG others(2160): Show |
chrX | 3036471 | 3117727 |
a0008c0020t0001 | 0/0 | 2165 | 1 | 0 | 0 | 1 | 0 | 0 | ARSF_chrX_3036471_3117727 | ARSF | AGTGG others(2160): Show |
chrX | 3036471 | 3117727 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0001 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | ARSF_chrX_3036471_3117727 | ARSF | chrX | 3036471 | 3117727 |
a0001c0001t0001g0002 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ARSF_chrX_3036471_3117727 | ARSF | chrX | 3036471 | 3117727 |
a0001c0001t0001g0003 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | ARSF_chrX_3036471_3117727 | ARSF | chrX | 3036471 | 3117727 |
a0001c0001t0001g0004 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ARSF_chrX_3036471_3117727 | ARSF | chrX | 3036471 | 3117727 |
a0001c0001t0001g0005 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ARSF_chrX_3036471_3117727 | ARSF | chrX | 3036471 | 3117727 |
a0001c0001t0001g0006 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ARSF_chrX_3036471_3117727 | ARSF | chrX | 3036471 | 3117727 |
a0001c0001t0001g0007 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ARSF_chrX_3036471_3117727 | ARSF | chrX | 3036471 | 3117727 |
a0001c0001t0001g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARSF_chrX_3036471_3117727 | ARSF | chrX | 3036471 | 3117727 |
a0001c0001t0001g0019 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARSF_chrX_3036471_3117727 | ARSF | chrX | 3036471 | 3117727 |
a0001c0001t0001g0020 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARSF_chrX_3036471_3117727 | ARSF | chrX | 3036471 | 3117727 |
a0001c0001t0001g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARSF_chrX_3036471_3117727 | ARSF | chrX | 3036471 | 3117727 |
a0001c0001t0001g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARSF_chrX_3036471_3117727 | ARSF | chrX | 3036471 | 3117727 |
a0001c0001t0001g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARSF_chrX_3036471_3117727 | ARSF | chrX | 3036471 | 3117727 |
a0001c0001t0001g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARSF_chrX_3036471_3117727 | ARSF | chrX | 3036471 | 3117727 |
a0001c0001t0001g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARSF_chrX_3036471_3117727 | ARSF | chrX | 3036471 | 3117727 |
a0001c0001t0001g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARSF_chrX_3036471_3117727 | ARSF | chrX | 3036471 | 3117727 |
a0001c0001t0001g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARSF_chrX_3036471_3117727 | ARSF | chrX | 3036471 | 3117727 |
a0001c0001t0001g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARSF_chrX_3036471_3117727 | ARSF | chrX | 3036471 | 3117727 |
a0001c0001t0001g0045 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARSF_chrX_3036471_3117727 | ARSF | chrX | 3036471 | 3117727 |
a0001c0001t0001g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARSF_chrX_3036471_3117727 | ARSF | chrX | 3036471 | 3117727 |
a0001c0001t0001g0047 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARSF_chrX_3036471_3117727 | ARSF | chrX | 3036471 | 3117727 |
a0001c0001t0001g0048 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARSF_chrX_3036471_3117727 | ARSF | chrX | 3036471 | 3117727 |
a0001c0001t0001g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARSF_chrX_3036471_3117727 | ARSF | chrX | 3036471 | 3117727 |
a0001c0001t0001g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARSF_chrX_3036471_3117727 | ARSF | chrX | 3036471 | 3117727 |
a0001c0001t0001g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARSF_chrX_3036471_3117727 | ARSF | chrX | 3036471 | 3117727 |
a0001c0001t0001g0053 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARSF_chrX_3036471_3117727 | ARSF | chrX | 3036471 | 3117727 |
a0001c0001t0001g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARSF_chrX_3036471_3117727 | ARSF | chrX | 3036471 | 3117727 |
a0001c0001t0001g0055 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARSF_chrX_3036471_3117727 | ARSF | chrX | 3036471 | 3117727 |
a0001c0001t0001g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARSF_chrX_3036471_3117727 | ARSF | chrX | 3036471 | 3117727 |
a0001c0001t0001g0057 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARSF_chrX_3036471_3117727 | ARSF | chrX | 3036471 | 3117727 |
a0001c0001t0001g0058 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARSF_chrX_3036471_3117727 | ARSF | chrX | 3036471 | 3117727 |
a0001c0001t0001g0059 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARSF_chrX_3036471_3117727 | ARSF | chrX | 3036471 | 3117727 |
a0001c0001t0001g0060 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARSF_chrX_3036471_3117727 | ARSF | chrX | 3036471 | 3117727 |
a0001c0001t0001g0061 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARSF_chrX_3036471_3117727 | ARSF | chrX | 3036471 | 3117727 |
a0001c0001t0001g0062 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARSF_chrX_3036471_3117727 | ARSF | chrX | 3036471 | 3117727 |
a0001c0001t0001g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARSF_chrX_3036471_3117727 | ARSF | chrX | 3036471 | 3117727 |
a0001c0001t0001g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARSF_chrX_3036471_3117727 | ARSF | chrX | 3036471 | 3117727 |
a0001c0001t0001g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARSF_chrX_3036471_3117727 | ARSF | chrX | 3036471 | 3117727 |
a0001c0001t0001g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARSF_chrX_3036471_3117727 | ARSF | chrX | 3036471 | 3117727 |
a0001c0001t0001g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARSF_chrX_3036471_3117727 | ARSF | chrX | 3036471 | 3117727 |
a0001c0001t0001g0069 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARSF_chrX_3036471_3117727 | ARSF | chrX | 3036471 | 3117727 |
a0001c0001t0001g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARSF_chrX_3036471_3117727 | ARSF | chrX | 3036471 | 3117727 |
a0001c0001t0001g0071 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARSF_chrX_3036471_3117727 | ARSF | chrX | 3036471 | 3117727 |
a0001c0001t0001g0072 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARSF_chrX_3036471_3117727 | ARSF | chrX | 3036471 | 3117727 |
a0001c0001t0001g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARSF_chrX_3036471_3117727 | ARSF | chrX | 3036471 | 3117727 |
a0001c0001t0001g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARSF_chrX_3036471_3117727 | ARSF | chrX | 3036471 | 3117727 |
a0001c0001t0001g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARSF_chrX_3036471_3117727 | ARSF | chrX | 3036471 | 3117727 |
a0001c0001t0001g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARSF_chrX_3036471_3117727 | ARSF | chrX | 3036471 | 3117727 |
a0001c0001t0001g0078 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARSF_chrX_3036471_3117727 | ARSF | chrX | 3036471 | 3117727 |
a0001c0001t0001g0079 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARSF_chrX_3036471_3117727 | ARSF | chrX | 3036471 | 3117727 |
a0001c0001t0001g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARSF_chrX_3036471_3117727 | ARSF | chrX | 3036471 | 3117727 |
a0001c0001t0001g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARSF_chrX_3036471_3117727 | ARSF | chrX | 3036471 | 3117727 |
a0001c0001t0001g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARSF_chrX_3036471_3117727 | ARSF | chrX | 3036471 | 3117727 |
a0001c0001t0001g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARSF_chrX_3036471_3117727 | ARSF | chrX | 3036471 | 3117727 |
a0001c0001t0001g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARSF_chrX_3036471_3117727 | ARSF | chrX | 3036471 | 3117727 |
a0001c0001t0001g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARSF_chrX_3036471_3117727 | ARSF | chrX | 3036471 | 3117727 |
a0001c0001t0001g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARSF_chrX_3036471_3117727 | ARSF | chrX | 3036471 | 3117727 |
a0001c0001t0001g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARSF_chrX_3036471_3117727 | ARSF | chrX | 3036471 | 3117727 |
a0001c0001t0001g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARSF_chrX_3036471_3117727 | ARSF | chrX | 3036471 | 3117727 |
a0001c0001t0001g0091 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARSF_chrX_3036471_3117727 | ARSF | chrX | 3036471 | 3117727 |
a0001c0001t0001g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARSF_chrX_3036471_3117727 | ARSF | chrX | 3036471 | 3117727 |
a0001c0001t0001g0093 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARSF_chrX_3036471_3117727 | ARSF | chrX | 3036471 | 3117727 |
a0001c0001t0001g0094 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARSF_chrX_3036471_3117727 | ARSF | chrX | 3036471 | 3117727 |
a0001c0001t0001g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARSF_chrX_3036471_3117727 | ARSF | chrX | 3036471 | 3117727 |
a0001c0001t0001g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARSF_chrX_3036471_3117727 | ARSF | chrX | 3036471 | 3117727 |
a0001c0001t0001g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARSF_chrX_3036471_3117727 | ARSF | chrX | 3036471 | 3117727 |
a0001c0001t0001g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARSF_chrX_3036471_3117727 | ARSF | chrX | 3036471 | 3117727 |
a0001c0001t0001g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARSF_chrX_3036471_3117727 | ARSF | chrX | 3036471 | 3117727 |
a0001c0001t0001g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARSF_chrX_3036471_3117727 | ARSF | chrX | 3036471 | 3117727 |
a0001c0001t0001g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARSF_chrX_3036471_3117727 | ARSF | chrX | 3036471 | 3117727 |
a0001c0001t0001g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARSF_chrX_3036471_3117727 | ARSF | chrX | 3036471 | 3117727 |
a0001c0001t0001g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARSF_chrX_3036471_3117727 | ARSF | chrX | 3036471 | 3117727 |
a0001c0001t0001g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARSF_chrX_3036471_3117727 | ARSF | chrX | 3036471 | 3117727 |
a0001c0001t0001g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARSF_chrX_3036471_3117727 | ARSF | chrX | 3036471 | 3117727 |
a0001c0001t0001g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARSF_chrX_3036471_3117727 | ARSF | chrX | 3036471 | 3117727 |
a0001c0001t0001g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARSF_chrX_3036471_3117727 | ARSF | chrX | 3036471 | 3117727 |
a0001c0001t0001g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARSF_chrX_3036471_3117727 | ARSF | chrX | 3036471 | 3117727 |
a0001c0001t0001g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARSF_chrX_3036471_3117727 | ARSF | chrX | 3036471 | 3117727 |
a0001c0001t0001g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARSF_chrX_3036471_3117727 | ARSF | chrX | 3036471 | 3117727 |
a0001c0001t0001g0117 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARSF_chrX_3036471_3117727 | ARSF | chrX | 3036471 | 3117727 |
a0001c0001t0001g0118 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARSF_chrX_3036471_3117727 | ARSF | chrX | 3036471 | 3117727 |
a0001c0001t0001g0119 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARSF_chrX_3036471_3117727 | ARSF | chrX | 3036471 | 3117727 |
a0001c0001t0001g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARSF_chrX_3036471_3117727 | ARSF | chrX | 3036471 | 3117727 |
a0001c0001t0001g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARSF_chrX_3036471_3117727 | ARSF | chrX | 3036471 | 3117727 |
a0001c0001t0001g0122 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARSF_chrX_3036471_3117727 | ARSF | chrX | 3036471 | 3117727 |
a0001c0001t0001g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARSF_chrX_3036471_3117727 | ARSF | chrX | 3036471 | 3117727 |
a0001c0001t0001g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARSF_chrX_3036471_3117727 | ARSF | chrX | 3036471 | 3117727 |
a0001c0001t0001g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARSF_chrX_3036471_3117727 | ARSF | chrX | 3036471 | 3117727 |
a0001c0001t0001g0126 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARSF_chrX_3036471_3117727 | ARSF | chrX | 3036471 | 3117727 |
a0001c0001t0001g0127 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARSF_chrX_3036471_3117727 | ARSF | chrX | 3036471 | 3117727 |
a0001c0001t0001g0132 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARSF_chrX_3036471_3117727 | ARSF | chrX | 3036471 | 3117727 |
a0001c0001t0001g0133 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARSF_chrX_3036471_3117727 | ARSF | chrX | 3036471 | 3117727 |
a0001c0001t0001g0134 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARSF_chrX_3036471_3117727 | ARSF | chrX | 3036471 | 3117727 |
a0001c0001t0001g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARSF_chrX_3036471_3117727 | ARSF | chrX | 3036471 | 3117727 |
a0001c0001t0001g0136 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARSF_chrX_3036471_3117727 | ARSF | chrX | 3036471 | 3117727 |
a0001c0001t0001g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARSF_chrX_3036471_3117727 | ARSF | chrX | 3036471 | 3117727 |
a0001c0001t0001g0138 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARSF_chrX_3036471_3117727 | ARSF | chrX | 3036471 | 3117727 |
a0001c0001t0001g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARSF_chrX_3036471_3117727 | ARSF | chrX | 3036471 | 3117727 |
a0001c0001t0001g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARSF_chrX_3036471_3117727 | ARSF | chrX | 3036471 | 3117727 |
a0001c0001t0001g0142 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARSF_chrX_3036471_3117727 | ARSF | chrX | 3036471 | 3117727 |
a0001c0001t0001g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARSF_chrX_3036471_3117727 | ARSF | chrX | 3036471 | 3117727 |
a0001c0001t0001g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARSF_chrX_3036471_3117727 | ARSF | chrX | 3036471 | 3117727 |
a0001c0001t0001g0146 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARSF_chrX_3036471_3117727 | ARSF | chrX | 3036471 | 3117727 |
a0001c0001t0001g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARSF_chrX_3036471_3117727 | ARSF | chrX | 3036471 | 3117727 |
a0001c0001t0001g0148 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARSF_chrX_3036471_3117727 | ARSF | chrX | 3036471 | 3117727 |
a0001c0001t0001g0149 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARSF_chrX_3036471_3117727 | ARSF | chrX | 3036471 | 3117727 |
a0001c0001t0001g0150 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARSF_chrX_3036471_3117727 | ARSF | chrX | 3036471 | 3117727 |
a0001c0001t0001g0151 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARSF_chrX_3036471_3117727 | ARSF | chrX | 3036471 | 3117727 |
a0001c0001t0001g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARSF_chrX_3036471_3117727 | ARSF | chrX | 3036471 | 3117727 |
a0001c0001t0001g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARSF_chrX_3036471_3117727 | ARSF | chrX | 3036471 | 3117727 |
a0001c0001t0001g0154 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARSF_chrX_3036471_3117727 | ARSF | chrX | 3036471 | 3117727 |
a0001c0001t0001g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARSF_chrX_3036471_3117727 | ARSF | chrX | 3036471 | 3117727 |
a0001c0001t0001g0157 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARSF_chrX_3036471_3117727 | ARSF | chrX | 3036471 | 3117727 |
a0001c0001t0001g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARSF_chrX_3036471_3117727 | ARSF | chrX | 3036471 | 3117727 |
a0001c0001t0001g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARSF_chrX_3036471_3117727 | ARSF | chrX | 3036471 | 3117727 |
a0001c0001t0001g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARSF_chrX_3036471_3117727 | ARSF | chrX | 3036471 | 3117727 |
a0001c0001t0001g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARSF_chrX_3036471_3117727 | ARSF | chrX | 3036471 | 3117727 |
a0001c0001t0001g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARSF_chrX_3036471_3117727 | ARSF | chrX | 3036471 | 3117727 |
a0001c0001t0001g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARSF_chrX_3036471_3117727 | ARSF | chrX | 3036471 | 3117727 |
a0001c0001t0001g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARSF_chrX_3036471_3117727 | ARSF | chrX | 3036471 | 3117727 |
a0001c0001t0001g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARSF_chrX_3036471_3117727 | ARSF | chrX | 3036471 | 3117727 |
a0001c0001t0001g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARSF_chrX_3036471_3117727 | ARSF | chrX | 3036471 | 3117727 |
a0001c0001t0001g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARSF_chrX_3036471_3117727 | ARSF | chrX | 3036471 | 3117727 |
a0001c0001t0001g0170 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARSF_chrX_3036471_3117727 | ARSF | chrX | 3036471 | 3117727 |
a0001c0001t0001g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARSF_chrX_3036471_3117727 | ARSF | chrX | 3036471 | 3117727 |
a0001c0001t0001g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARSF_chrX_3036471_3117727 | ARSF | chrX | 3036471 | 3117727 |
a0001c0001t0001g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARSF_chrX_3036471_3117727 | ARSF | chrX | 3036471 | 3117727 |
a0001c0001t0001g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARSF_chrX_3036471_3117727 | ARSF | chrX | 3036471 | 3117727 |
a0001c0001t0001g0176 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARSF_chrX_3036471_3117727 | ARSF | chrX | 3036471 | 3117727 |
a0001c0001t0001g0177 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARSF_chrX_3036471_3117727 | ARSF | chrX | 3036471 | 3117727 |
a0001c0001t0001g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARSF_chrX_3036471_3117727 | ARSF | chrX | 3036471 | 3117727 |
a0001c0001t0001g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARSF_chrX_3036471_3117727 | ARSF | chrX | 3036471 | 3117727 |
a0001c0001t0004g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARSF_chrX_3036471_3117727 | ARSF | chrX | 3036471 | 3117727 |
a0001c0001t0005g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARSF_chrX_3036471_3117727 | ARSF | chrX | 3036471 | 3117727 |
a0001c0002t0001g0014 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARSF_chrX_3036471_3117727 | ARSF | chrX | 3036471 | 3117727 |
a0001c0002t0001g0015 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARSF_chrX_3036471_3117727 | ARSF | chrX | 3036471 | 3117727 |
a0001c0002t0001g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARSF_chrX_3036471_3117727 | ARSF | chrX | 3036471 | 3117727 |
a0001c0002t0001g0023 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | ARSF_chrX_3036471_3117727 | ARSF | chrX | 3036471 | 3117727 |
a0001c0002t0001g0024 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARSF_chrX_3036471_3117727 | ARSF | chrX | 3036471 | 3117727 |
a0001c0002t0001g0026 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARSF_chrX_3036471_3117727 | ARSF | chrX | 3036471 | 3117727 |
a0001c0002t0001g0028 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARSF_chrX_3036471_3117727 | ARSF | chrX | 3036471 | 3117727 |
a0001c0002t0001g0029 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | ARSF_chrX_3036471_3117727 | ARSF | chrX | 3036471 | 3117727 |
a0001c0002t0001g0030 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARSF_chrX_3036471_3117727 | ARSF | chrX | 3036471 | 3117727 |
a0001c0002t0001g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARSF_chrX_3036471_3117727 | ARSF | chrX | 3036471 | 3117727 |
a0001c0002t0001g0128 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARSF_chrX_3036471_3117727 | ARSF | chrX | 3036471 | 3117727 |
a0001c0002t0001g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARSF_chrX_3036471_3117727 | ARSF | chrX | 3036471 | 3117727 |
a0001c0002t0001g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARSF_chrX_3036471_3117727 | ARSF | chrX | 3036471 | 3117727 |
a0001c0002t0001g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARSF_chrX_3036471_3117727 | ARSF | chrX | 3036471 | 3117727 |
a0001c0002t0001g0185 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARSF_chrX_3036471_3117727 | ARSF | chrX | 3036471 | 3117727 |
a0001c0005t0001g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARSF_chrX_3036471_3117727 | ARSF | chrX | 3036471 | 3117727 |
a0001c0005t0001g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARSF_chrX_3036471_3117727 | ARSF | chrX | 3036471 | 3117727 |
a0001c0005t0001g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARSF_chrX_3036471_3117727 | ARSF | chrX | 3036471 | 3117727 |
a0001c0005t0001g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARSF_chrX_3036471_3117727 | ARSF | chrX | 3036471 | 3117727 |
a0001c0007t0003g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARSF_chrX_3036471_3117727 | ARSF | chrX | 3036471 | 3117727 |
a0001c0007t0003g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARSF_chrX_3036471_3117727 | ARSF | chrX | 3036471 | 3117727 |
a0001c0009t0001g0016 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARSF_chrX_3036471_3117727 | ARSF | chrX | 3036471 | 3117727 |
a0001c0009t0001g0018 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARSF_chrX_3036471_3117727 | ARSF | chrX | 3036471 | 3117727 |
a0001c0010t0001g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARSF_chrX_3036471_3117727 | ARSF | chrX | 3036471 | 3117727 |
a0001c0010t0001g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARSF_chrX_3036471_3117727 | ARSF | chrX | 3036471 | 3117727 |
a0001c0012t0001g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARSF_chrX_3036471_3117727 | ARSF | chrX | 3036471 | 3117727 |
a0001c0015t0006g0021 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARSF_chrX_3036471_3117727 | ARSF | chrX | 3036471 | 3117727 |
a0001c0016t0001g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARSF_chrX_3036471_3117727 | ARSF | chrX | 3036471 | 3117727 |
a0001c0019t0001g0095 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ARSF_chrX_3036471_3117727 | ARSF | chrX | 3036471 | 3117727 |
a0002c0003t0001g0013 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARSF_chrX_3036471_3117727 | ARSF | chrX | 3036471 | 3117727 |
a0002c0003t0001g0017 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARSF_chrX_3036471_3117727 | ARSF | chrX | 3036471 | 3117727 |
a0002c0003t0001g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARSF_chrX_3036471_3117727 | ARSF | chrX | 3036471 | 3117727 |
a0002c0003t0001g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARSF_chrX_3036471_3117727 | ARSF | chrX | 3036471 | 3117727 |
a0002c0003t0001g0144 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARSF_chrX_3036471_3117727 | ARSF | chrX | 3036471 | 3117727 |
a0002c0004t0001g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARSF_chrX_3036471_3117727 | ARSF | chrX | 3036471 | 3117727 |
a0002c0004t0001g0129 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ARSF_chrX_3036471_3117727 | ARSF | chrX | 3036471 | 3117727 |
a0002c0004t0001g0179 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARSF_chrX_3036471_3117727 | ARSF | chrX | 3036471 | 3117727 |
a0002c0004t0001g0180 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARSF_chrX_3036471_3117727 | ARSF | chrX | 3036471 | 3117727 |
a0003c0008t0001g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARSF_chrX_3036471_3117727 | ARSF | chrX | 3036471 | 3117727 |
a0003c0008t0001g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARSF_chrX_3036471_3117727 | ARSF | chrX | 3036471 | 3117727 |
a0003c0013t0001g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARSF_chrX_3036471_3117727 | ARSF | chrX | 3036471 | 3117727 |
a0003c0017t0001g0139 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARSF_chrX_3036471_3117727 | ARSF | chrX | 3036471 | 3117727 |
a0004c0006t0001g0008 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARSF_chrX_3036471_3117727 | ARSF | chrX | 3036471 | 3117727 |
a0004c0006t0001g0009 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ARSF_chrX_3036471_3117727 | ARSF | chrX | 3036471 | 3117727 |
a0004c0006t0001g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARSF_chrX_3036471_3117727 | ARSF | chrX | 3036471 | 3117727 |
a0005c0011t0001g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARSF_chrX_3036471_3117727 | ARSF | chrX | 3036471 | 3117727 |
a0005c0011t0001g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARSF_chrX_3036471_3117727 | ARSF | chrX | 3036471 | 3117727 |
a0005c0022t0001g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARSF_chrX_3036471_3117727 | ARSF | chrX | 3036471 | 3117727 |
a0006c0014t0002g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARSF_chrX_3036471_3117727 | ARSF | chrX | 3036471 | 3117727 |
a0006c0018t0002g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ARSF_chrX_3036471_3117727 | ARSF | chrX | 3036471 | 3117727 |
a0007c0021t0001g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARSF_chrX_3036471_3117727 | ARSF | chrX | 3036471 | 3117727 |
a0008c0020t0001g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ARSF_chrX_3036471_3117727 | ARSF | chrX | 3036471 | 3117727 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0001 | c0002 | t0001 | g0026 | EUR | GBR | ARSF_chrX_3036471_3117727 | ARSF | chrX | 3036471 | 3117727 |
HG00099 | hp2 | a0002 | c0004 | t0001 | g0129 | EUR | GBR | ARSF_chrX_3036471_3117727 | ARSF | chrX | 3036471 | 3117727 |
HG00140 | hp1 | a0001 | c0001 | t0001 | g0133 | EUR | GBR | ARSF_chrX_3036471_3117727 | ARSF | chrX | 3036471 | 3117727 |
HG00280 | hp1 | a0001 | c0001 | t0001 | g0093 | EUR | FIN | ARSF_chrX_3036471_3117727 | ARSF | chrX | 3036471 | 3117727 |
HG00323 | hp1 | a0001 | c0002 | t0001 | g0024 | EUR | FIN | ARSF_chrX_3036471_3117727 | ARSF | chrX | 3036471 | 3117727 |
HG00323 | hp2 | a0001 | c0001 | t0001 | g0062 | EUR | FIN | ARSF_chrX_3036471_3117727 | ARSF | chrX | 3036471 | 3117727 |
HG00597 | hp1 | a0007 | c0021 | t0001 | g0174 | EAS | CHS | ARSF_chrX_3036471_3117727 | ARSF | chrX | 3036471 | 3117727 |
HG00597 | hp2 | a0001 | c0001 | t0001 | g0101 | EAS | CHS | ARSF_chrX_3036471_3117727 | ARSF | chrX | 3036471 | 3117727 |
HG00609 | hp1 | a0001 | c0001 | t0001 | g0160 | EAS | CHS | ARSF_chrX_3036471_3117727 | ARSF | chrX | 3036471 | 3117727 |
HG00621 | hp1 | a0001 | c0001 | t0001 | g0102 | EAS | CHS | ARSF_chrX_3036471_3117727 | ARSF | chrX | 3036471 | 3117727 |
HG00642 | hp1 | a0001 | c0002 | t0001 | g0028 | AMR | PUR | ARSF_chrX_3036471_3117727 | ARSF | chrX | 3036471 | 3117727 |
HG00673 | hp1 | a0008 | c0020 | t0001 | g0104 | EAS | CHS | ARSF_chrX_3036471_3117727 | ARSF | chrX | 3036471 | 3117727 |
HG00735 | hp1 | a0001 | c0002 | t0001 | g0014 | AMR | PUR | ARSF_chrX_3036471_3117727 | ARSF | chrX | 3036471 | 3117727 |
HG00735 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | ARSF_chrX_3036471_3117727 | ARSF | chrX | 3036471 | 3117727 |
HG00738 | hp1 | a0001 | c0001 | t0001 | g0047 | AMR | PUR | ARSF_chrX_3036471_3117727 | ARSF | chrX | 3036471 | 3117727 |
HG00741 | hp1 | a0001 | c0001 | t0001 | g0118 | AMR | PUR | ARSF_chrX_3036471_3117727 | ARSF | chrX | 3036471 | 3117727 |
HG00741 | hp2 | a0001 | c0001 | t0001 | g0020 | AMR | PUR | ARSF_chrX_3036471_3117727 | ARSF | chrX | 3036471 | 3117727 |
HG01069 | hp1 | a0001 | c0001 | t0001 | g0057 | AMR | PUR | ARSF_chrX_3036471_3117727 | ARSF | chrX | 3036471 | 3117727 |
HG01070 | hp1 | a0002 | c0004 | t0001 | g0180 | AMR | PUR | ARSF_chrX_3036471_3117727 | ARSF | chrX | 3036471 | 3117727 |
HG01070 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | ARSF_chrX_3036471_3117727 | ARSF | chrX | 3036471 | 3117727 |
HG01071 | hp1 | a0001 | c0001 | t0001 | g0058 | AMR | PUR | ARSF_chrX_3036471_3117727 | ARSF | chrX | 3036471 | 3117727 |
HG01071 | hp2 | a0002 | c0004 | t0001 | g0179 | AMR | PUR | ARSF_chrX_3036471_3117727 | ARSF | chrX | 3036471 | 3117727 |
HG01074 | hp1 | a0003 | c0017 | t0001 | g0139 | AMR | PUR | ARSF_chrX_3036471_3117727 | ARSF | chrX | 3036471 | 3117727 |
HG01099 | hp1 | a0001 | c0001 | t0001 | g0127 | AMR | PUR | ARSF_chrX_3036471_3117727 | ARSF | chrX | 3036471 | 3117727 |
HG01106 | hp1 | a0001 | c0001 | t0001 | g0063 | AMR | PUR | ARSF_chrX_3036471_3117727 | ARSF | chrX | 3036471 | 3117727 |
HG01109 | hp1 | a0001 | c0002 | t0001 | g0185 | AMR | PUR | ARSF_chrX_3036471_3117727 | ARSF | chrX | 3036471 | 3117727 |
HG01167 | hp1 | a0002 | c0003 | t0001 | g0013 | AMR | PUR | ARSF_chrX_3036471_3117727 | ARSF | chrX | 3036471 | 3117727 |
HG01168 | hp1 | a0004 | c0006 | t0001 | g0009 | AMR | PUR | ARSF_chrX_3036471_3117727 | ARSF | chrX | 3036471 | 3117727 |
HG01168 | hp2 | a0001 | c0001 | t0001 | g0019 | AMR | PUR | ARSF_chrX_3036471_3117727 | ARSF | chrX | 3036471 | 3117727 |
HG01169 | hp1 | a0002 | c0003 | t0001 | g0017 | AMR | PUR | ARSF_chrX_3036471_3117727 | ARSF | chrX | 3036471 | 3117727 |
HG01169 | hp2 | a0004 | c0006 | t0001 | g0008 | AMR | PUR | ARSF_chrX_3036471_3117727 | ARSF | chrX | 3036471 | 3117727 |
HG01192 | hp1 | a0001 | c0001 | t0001 | g0157 | AMR | PUR | ARSF_chrX_3036471_3117727 | ARSF | chrX | 3036471 | 3117727 |
HG01255 | hp1 | a0001 | c0001 | t0001 | g0053 | AMR | CLM | ARSF_chrX_3036471_3117727 | ARSF | chrX | 3036471 | 3117727 |
HG01256 | hp1 | a0001 | c0001 | t0001 | g0048 | AMR | CLM | ARSF_chrX_3036471_3117727 | ARSF | chrX | 3036471 | 3117727 |
HG01258 | hp1 | a0001 | c0001 | t0001 | g0151 | AMR | CLM | ARSF_chrX_3036471_3117727 | ARSF | chrX | 3036471 | 3117727 |
HG01358 | hp1 | a0001 | c0001 | t0001 | g0059 | AMR | CLM | ARSF_chrX_3036471_3117727 | ARSF | chrX | 3036471 | 3117727 |
HG01496 | hp1 | a0001 | c0001 | t0001 | g0061 | AMR | CLM | ARSF_chrX_3036471_3117727 | ARSF | chrX | 3036471 | 3117727 |
HG01496 | hp2 | a0002 | c0003 | t0001 | g0144 | AMR | CLM | ARSF_chrX_3036471_3117727 | ARSF | chrX | 3036471 | 3117727 |
HG01515 | hp1 | a0001 | c0001 | t0001 | g0150 | EUR | IBS | ARSF_chrX_3036471_3117727 | ARSF | chrX | 3036471 | 3117727 |
HG01517 | hp1 | a0001 | c0001 | t0001 | g0138 | EUR | IBS | ARSF_chrX_3036471_3117727 | ARSF | chrX | 3036471 | 3117727 |
HG01517 | hp2 | a0001 | c0001 | t0001 | g0149 | EUR | IBS | ARSF_chrX_3036471_3117727 | ARSF | chrX | 3036471 | 3117727 |
HG01884 | hp1 | a0006 | c0014 | t0002 | g0025 | AFR | ACB | ARSF_chrX_3036471_3117727 | ARSF | chrX | 3036471 | 3117727 |
HG01884 | hp2 | a0001 | c0001 | t0001 | g0044 | AFR | ACB | ARSF_chrX_3036471_3117727 | ARSF | chrX | 3036471 | 3117727 |
HG01934 | hp1 | a0001 | c0001 | t0001 | g0176 | AMR | PEL | ARSF_chrX_3036471_3117727 | ARSF | chrX | 3036471 | 3117727 |
HG01943 | hp1 | a0001 | c0001 | t0001 | g0055 | AMR | PEL | ARSF_chrX_3036471_3117727 | ARSF | chrX | 3036471 | 3117727 |
HG01952 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | ARSF_chrX_3036471_3117727 | ARSF | chrX | 3036471 | 3117727 |
HG01978 | hp1 | a0001 | c0001 | t0001 | g0126 | AMR | PEL | ARSF_chrX_3036471_3117727 | ARSF | chrX | 3036471 | 3117727 |
HG01978 | hp2 | a0001 | c0001 | t0001 | g0096 | AMR | PEL | ARSF_chrX_3036471_3117727 | ARSF | chrX | 3036471 | 3117727 |
HG02015 | hp1 | a0001 | c0001 | t0001 | g0171 | EAS | KHV | ARSF_chrX_3036471_3117727 | ARSF | chrX | 3036471 | 3117727 |
HG02027 | hp1 | a0001 | c0001 | t0001 | g0103 | EAS | KHV | ARSF_chrX_3036471_3117727 | ARSF | chrX | 3036471 | 3117727 |
HG02040 | hp1 | a0001 | c0001 | t0001 | g0097 | EAS | KHV | ARSF_chrX_3036471_3117727 | ARSF | chrX | 3036471 | 3117727 |
HG02055 | hp1 | a0001 | c0001 | t0001 | g0162 | AFR | ACB | ARSF_chrX_3036471_3117727 | ARSF | chrX | 3036471 | 3117727 |
HG02056 | hp1 | a0001 | c0001 | t0001 | g0161 | EAS | KHV | ARSF_chrX_3036471_3117727 | ARSF | chrX | 3036471 | 3117727 |
HG02071 | hp1 | a0001 | c0001 | t0001 | g0086 | EAS | KHV | ARSF_chrX_3036471_3117727 | ARSF | chrX | 3036471 | 3117727 |
HG02074 | hp1 | a0001 | c0001 | t0001 | g0159 | EAS | KHV | ARSF_chrX_3036471_3117727 | ARSF | chrX | 3036471 | 3117727 |
HG02083 | hp1 | a0002 | c0003 | t0001 | g0106 | EAS | KHV | ARSF_chrX_3036471_3117727 | ARSF | chrX | 3036471 | 3117727 |
HG02129 | hp1 | a0001 | c0001 | t0001 | g0124 | EAS | KHV | ARSF_chrX_3036471_3117727 | ARSF | chrX | 3036471 | 3117727 |
HG02132 | hp1 | a0001 | c0001 | t0001 | g0105 | EAS | KHV | ARSF_chrX_3036471_3117727 | ARSF | chrX | 3036471 | 3117727 |
HG02135 | hp1 | a0001 | c0001 | t0001 | g0172 | EAS | KHV | ARSF_chrX_3036471_3117727 | ARSF | chrX | 3036471 | 3117727 |
HG02257 | hp1 | a0001 | c0001 | t0001 | g0140 | AFR | ACB | ARSF_chrX_3036471_3117727 | ARSF | chrX | 3036471 | 3117727 |
HG02257 | hp2 | a0001 | c0007 | t0003 | g0031 | AFR | ACB | ARSF_chrX_3036471_3117727 | ARSF | chrX | 3036471 | 3117727 |
HG02258 | hp1 | a0003 | c0008 | t0001 | g0115 | AFR | ACB | ARSF_chrX_3036471_3117727 | ARSF | chrX | 3036471 | 3117727 |
HG02280 | hp1 | a0001 | c0010 | t0001 | g0033 | AFR | ACB | ARSF_chrX_3036471_3117727 | ARSF | chrX | 3036471 | 3117727 |
HG02280 | hp2 | a0001 | c0016 | t0001 | g0155 | AFR | ACB | ARSF_chrX_3036471_3117727 | ARSF | chrX | 3036471 | 3117727 |
HG02300 | hp1 | a0001 | c0002 | t0001 | g0128 | AMR | PEL | ARSF_chrX_3036471_3117727 | ARSF | chrX | 3036471 | 3117727 |
HG02451 | hp1 | a0001 | c0001 | t0001 | g0038 | AFR | ACB | ARSF_chrX_3036471_3117727 | ARSF | chrX | 3036471 | 3117727 |
HG02451 | hp2 | a0006 | c0018 | t0002 | g0131 | AFR | ACB | ARSF_chrX_3036471_3117727 | ARSF | chrX | 3036471 | 3117727 |
HG02572 | hp1 | a0005 | c0011 | t0001 | g0027 | AFR | GWD | ARSF_chrX_3036471_3117727 | ARSF | chrX | 3036471 | 3117727 |
HG02602 | hp1 | a0001 | c0001 | t0001 | g0170 | SAS | PJL | ARSF_chrX_3036471_3117727 | ARSF | chrX | 3036471 | 3117727 |
HG02622 | hp1 | a0002 | c0004 | t0001 | g0090 | AFR | GWD | ARSF_chrX_3036471_3117727 | ARSF | chrX | 3036471 | 3117727 |
HG02622 | hp2 | a0001 | c0002 | t0001 | g0184 | AFR | GWD | ARSF_chrX_3036471_3117727 | ARSF | chrX | 3036471 | 3117727 |
HG02647 | hp1 | a0001 | c0001 | t0001 | g0065 | AFR | GWD | ARSF_chrX_3036471_3117727 | ARSF | chrX | 3036471 | 3117727 |
HG02683 | hp1 | a0001 | c0002 | t0001 | g0015 | SAS | PJL | ARSF_chrX_3036471_3117727 | ARSF | chrX | 3036471 | 3117727 |
HG02683 | hp2 | a0001 | c0001 | t0001 | g0136 | SAS | PJL | ARSF_chrX_3036471_3117727 | ARSF | chrX | 3036471 | 3117727 |
HG02698 | hp1 | a0001 | c0001 | t0001 | g0069 | SAS | PJL | ARSF_chrX_3036471_3117727 | ARSF | chrX | 3036471 | 3117727 |
HG02735 | hp1 | a0001 | c0019 | t0001 | g0095 | SAS | PJL | ARSF_chrX_3036471_3117727 | ARSF | chrX | 3036471 | 3117727 |
HG02738 | hp1 | a0001 | c0001 | t0001 | g0132 | SAS | PJL | ARSF_chrX_3036471_3117727 | ARSF | chrX | 3036471 | 3117727 |
HG02809 | hp1 | a0001 | c0010 | t0001 | g0040 | AFR | GWD | ARSF_chrX_3036471_3117727 | ARSF | chrX | 3036471 | 3117727 |
HG02809 | hp2 | a0001 | c0001 | t0001 | g0135 | AFR | GWD | ARSF_chrX_3036471_3117727 | ARSF | chrX | 3036471 | 3117727 |
HG02895 | hp1 | a0001 | c0001 | t0001 | g0036 | AFR | GWD | ARSF_chrX_3036471_3117727 | ARSF | chrX | 3036471 | 3117727 |
HG02896 | hp1 | a0001 | c0001 | t0001 | g0051 | AFR | GWD | ARSF_chrX_3036471_3117727 | ARSF | chrX | 3036471 | 3117727 |
HG02896 | hp2 | a0001 | c0002 | t0001 | g0183 | AFR | GWD | ARSF_chrX_3036471_3117727 | ARSF | chrX | 3036471 | 3117727 |
HG02897 | hp1 | a0001 | c0002 | t0001 | g0181 | AFR | GWD | ARSF_chrX_3036471_3117727 | ARSF | chrX | 3036471 | 3117727 |
HG02897 | hp2 | a0001 | c0001 | t0001 | g0037 | AFR | GWD | ARSF_chrX_3036471_3117727 | ARSF | chrX | 3036471 | 3117727 |
HG02922 | hp1 | a0001 | c0005 | t0001 | g0043 | AFR | ESN | ARSF_chrX_3036471_3117727 | ARSF | chrX | 3036471 | 3117727 |
HG02922 | hp2 | a0001 | c0001 | t0001 | g0041 | AFR | ESN | ARSF_chrX_3036471_3117727 | ARSF | chrX | 3036471 | 3117727 |
HG02965 | hp1 | a0001 | c0007 | t0003 | g0182 | AFR | ESN | ARSF_chrX_3036471_3117727 | ARSF | chrX | 3036471 | 3117727 |
HG03017 | hp1 | a0001 | c0001 | t0001 | g0117 | SAS | PJL | ARSF_chrX_3036471_3117727 | ARSF | chrX | 3036471 | 3117727 |
HG03041 | hp1 | a0001 | c0005 | t0001 | g0012 | AFR | GWD | ARSF_chrX_3036471_3117727 | ARSF | chrX | 3036471 | 3117727 |
HG03041 | hp2 | a0005 | c0022 | t0001 | g0169 | AFR | GWD | ARSF_chrX_3036471_3117727 | ARSF | chrX | 3036471 | 3117727 |
HG03098 | hp1 | a0001 | c0005 | t0001 | g0042 | AFR | MSL | ARSF_chrX_3036471_3117727 | ARSF | chrX | 3036471 | 3117727 |
HG03130 | hp1 | a0001 | c0001 | t0001 | g0039 | AFR | ESN | ARSF_chrX_3036471_3117727 | ARSF | chrX | 3036471 | 3117727 |
HG03139 | hp1 | a0003 | c0008 | t0001 | g0167 | AFR | ESN | ARSF_chrX_3036471_3117727 | ARSF | chrX | 3036471 | 3117727 |
HG03209 | hp1 | a0001 | c0001 | t0001 | g0006 | AFR | MSL | ARSF_chrX_3036471_3117727 | ARSF | chrX | 3036471 | 3117727 |
HG03225 | hp1 | a0002 | c0003 | t0001 | g0050 | AFR | MSL | ARSF_chrX_3036471_3117727 | ARSF | chrX | 3036471 | 3117727 |
HG03239 | hp1 | a0001 | c0001 | t0001 | g0177 | SAS | PJL | ARSF_chrX_3036471_3117727 | ARSF | chrX | 3036471 | 3117727 |
HG03239 | hp2 | a0001 | c0015 | t0006 | g0021 | SAS | PJL | ARSF_chrX_3036471_3117727 | ARSF | chrX | 3036471 | 3117727 |
HG03490 | hp1 | a0001 | c0001 | t0001 | g0122 | SAS | PJL | ARSF_chrX_3036471_3117727 | ARSF | chrX | 3036471 | 3117727 |
HG03491 | hp1 | a0001 | c0009 | t0001 | g0016 | SAS | PJL | ARSF_chrX_3036471_3117727 | ARSF | chrX | 3036471 | 3117727 |
HG03491 | hp2 | a0001 | c0001 | t0001 | g0079 | SAS | PJL | ARSF_chrX_3036471_3117727 | ARSF | chrX | 3036471 | 3117727 |
HG03492 | hp1 | a0001 | c0009 | t0001 | g0018 | SAS | PJL | ARSF_chrX_3036471_3117727 | ARSF | chrX | 3036471 | 3117727 |
HG03654 | hp1 | a0001 | c0001 | t0001 | g0045 | SAS | PJL | ARSF_chrX_3036471_3117727 | ARSF | chrX | 3036471 | 3117727 |
HG03669 | hp1 | a0001 | c0001 | t0001 | g0148 | SAS | PJL | ARSF_chrX_3036471_3117727 | ARSF | chrX | 3036471 | 3117727 |
HG03669 | hp2 | a0001 | c0001 | t0001 | g0119 | SAS | PJL | ARSF_chrX_3036471_3117727 | ARSF | chrX | 3036471 | 3117727 |
HG03688 | hp1 | a0001 | c0002 | t0001 | g0030 | SAS | STU | ARSF_chrX_3036471_3117727 | ARSF | chrX | 3036471 | 3117727 |
HG03704 | hp1 | a0001 | c0001 | t0001 | g0154 | SAS | PJL | ARSF_chrX_3036471_3117727 | ARSF | chrX | 3036471 | 3117727 |
HG03704 | hp2 | a0001 | c0001 | t0001 | g0071 | SAS | PJL | ARSF_chrX_3036471_3117727 | ARSF | chrX | 3036471 | 3117727 |
HG03710 | hp1 | a0001 | c0001 | t0001 | g0142 | SAS | PJL | ARSF_chrX_3036471_3117727 | ARSF | chrX | 3036471 | 3117727 |
HG03942 | hp1 | a0001 | c0001 | t0001 | g0078 | SAS | BEB | ARSF_chrX_3036471_3117727 | ARSF | chrX | 3036471 | 3117727 |
HG04115 | hp1 | a0001 | c0001 | t0001 | g0094 | SAS | STU | ARSF_chrX_3036471_3117727 | ARSF | chrX | 3036471 | 3117727 |
HG04199 | hp1 | a0001 | c0001 | t0001 | g0072 | SAS | STU | ARSF_chrX_3036471_3117727 | ARSF | chrX | 3036471 | 3117727 |
HG04204 | hp1 | a0001 | c0001 | t0001 | g0134 | SAS | STU | ARSF_chrX_3036471_3117727 | ARSF | chrX | 3036471 | 3117727 |
HG04228 | hp1 | a0001 | c0001 | t0001 | g0003 | SAS | STU | ARSF_chrX_3036471_3117727 | ARSF | chrX | 3036471 | 3117727 |
NA18522 | hp1 | a0001 | c0001 | t0001 | g0164 | AFR | YRI | ARSF_chrX_3036471_3117727 | ARSF | chrX | 3036471 | 3117727 |
NA18612 | hp1 | a0001 | c0001 | t0001 | g0084 | EAS | CHB | ARSF_chrX_3036471_3117727 | ARSF | chrX | 3036471 | 3117727 |
NA18747 | hp1 | a0001 | c0001 | t0001 | g0054 | EAS | CHB | ARSF_chrX_3036471_3117727 | ARSF | chrX | 3036471 | 3117727 |
NA18940 | hp1 | a0001 | c0001 | t0001 | g0143 | EAS | JPT | ARSF_chrX_3036471_3117727 | ARSF | chrX | 3036471 | 3117727 |
NA18943 | hp1 | a0001 | c0001 | t0001 | g0100 | EAS | JPT | ARSF_chrX_3036471_3117727 | ARSF | chrX | 3036471 | 3117727 |
NA18944 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | ARSF_chrX_3036471_3117727 | ARSF | chrX | 3036471 | 3117727 |
NA18945 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | ARSF_chrX_3036471_3117727 | ARSF | chrX | 3036471 | 3117727 |
NA18946 | hp1 | a0001 | c0001 | t0001 | g0109 | EAS | JPT | ARSF_chrX_3036471_3117727 | ARSF | chrX | 3036471 | 3117727 |
NA18946 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | ARSF_chrX_3036471_3117727 | ARSF | chrX | 3036471 | 3117727 |
NA18948 | hp1 | a0001 | c0001 | t0001 | g0052 | EAS | JPT | ARSF_chrX_3036471_3117727 | ARSF | chrX | 3036471 | 3117727 |
NA18951 | hp1 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | ARSF_chrX_3036471_3117727 | ARSF | chrX | 3036471 | 3117727 |
NA18951 | hp2 | a0001 | c0001 | t0001 | g0141 | EAS | JPT | ARSF_chrX_3036471_3117727 | ARSF | chrX | 3036471 | 3117727 |
NA18952 | hp1 | a0001 | c0001 | t0001 | g0083 | EAS | JPT | ARSF_chrX_3036471_3117727 | ARSF | chrX | 3036471 | 3117727 |
NA18953 | hp1 | a0001 | c0001 | t0001 | g0116 | EAS | JPT | ARSF_chrX_3036471_3117727 | ARSF | chrX | 3036471 | 3117727 |
NA18957 | hp1 | a0001 | c0001 | t0001 | g0110 | EAS | JPT | ARSF_chrX_3036471_3117727 | ARSF | chrX | 3036471 | 3117727 |
NA18957 | hp2 | a0001 | c0001 | t0001 | g0085 | EAS | JPT | ARSF_chrX_3036471_3117727 | ARSF | chrX | 3036471 | 3117727 |
NA18959 | hp1 | a0001 | c0001 | t0001 | g0153 | EAS | JPT | ARSF_chrX_3036471_3117727 | ARSF | chrX | 3036471 | 3117727 |
NA18960 | hp1 | a0001 | c0001 | t0001 | g0114 | EAS | JPT | ARSF_chrX_3036471_3117727 | ARSF | chrX | 3036471 | 3117727 |
NA18961 | hp1 | a0001 | c0001 | t0001 | g0081 | EAS | JPT | ARSF_chrX_3036471_3117727 | ARSF | chrX | 3036471 | 3117727 |
NA18962 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ARSF_chrX_3036471_3117727 | ARSF | chrX | 3036471 | 3117727 |
NA18965 | hp1 | a0001 | c0001 | t0001 | g0121 | EAS | JPT | ARSF_chrX_3036471_3117727 | ARSF | chrX | 3036471 | 3117727 |
NA18970 | hp1 | a0001 | c0001 | t0001 | g0099 | EAS | JPT | ARSF_chrX_3036471_3117727 | ARSF | chrX | 3036471 | 3117727 |
NA18971 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | ARSF_chrX_3036471_3117727 | ARSF | chrX | 3036471 | 3117727 |
NA18974 | hp1 | a0001 | c0001 | t0001 | g0088 | EAS | JPT | ARSF_chrX_3036471_3117727 | ARSF | chrX | 3036471 | 3117727 |
NA18977 | hp1 | a0001 | c0001 | t0001 | g0092 | EAS | JPT | ARSF_chrX_3036471_3117727 | ARSF | chrX | 3036471 | 3117727 |
NA18982 | hp1 | a0001 | c0001 | t0001 | g0087 | EAS | JPT | ARSF_chrX_3036471_3117727 | ARSF | chrX | 3036471 | 3117727 |
NA18983 | hp1 | a0001 | c0001 | t0001 | g0145 | EAS | JPT | ARSF_chrX_3036471_3117727 | ARSF | chrX | 3036471 | 3117727 |
NA18984 | hp1 | a0001 | c0001 | t0001 | g0125 | EAS | JPT | ARSF_chrX_3036471_3117727 | ARSF | chrX | 3036471 | 3117727 |
NA18986 | hp1 | a0001 | c0001 | t0001 | g0064 | EAS | JPT | ARSF_chrX_3036471_3117727 | ARSF | chrX | 3036471 | 3117727 |
NA18988 | hp1 | a0001 | c0001 | t0001 | g0112 | EAS | JPT | ARSF_chrX_3036471_3117727 | ARSF | chrX | 3036471 | 3117727 |
NA18989 | hp1 | a0001 | c0001 | t0001 | g0163 | EAS | JPT | ARSF_chrX_3036471_3117727 | ARSF | chrX | 3036471 | 3117727 |
NA18990 | hp1 | a0001 | c0001 | t0001 | g0082 | EAS | JPT | ARSF_chrX_3036471_3117727 | ARSF | chrX | 3036471 | 3117727 |
NA18994 | hp1 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | ARSF_chrX_3036471_3117727 | ARSF | chrX | 3036471 | 3117727 |
NA18995 | hp1 | a0001 | c0001 | t0001 | g0066 | EAS | JPT | ARSF_chrX_3036471_3117727 | ARSF | chrX | 3036471 | 3117727 |
NA18998 | hp1 | a0001 | c0001 | t0001 | g0074 | EAS | JPT | ARSF_chrX_3036471_3117727 | ARSF | chrX | 3036471 | 3117727 |
NA18998 | hp2 | a0001 | c0001 | t0001 | g0173 | EAS | JPT | ARSF_chrX_3036471_3117727 | ARSF | chrX | 3036471 | 3117727 |
NA19000 | hp1 | a0001 | c0001 | t0001 | g0166 | EAS | JPT | ARSF_chrX_3036471_3117727 | ARSF | chrX | 3036471 | 3117727 |
NA19003 | hp1 | a0001 | c0001 | t0001 | g0049 | EAS | JPT | ARSF_chrX_3036471_3117727 | ARSF | chrX | 3036471 | 3117727 |
NA19003 | hp2 | a0001 | c0001 | t0001 | g0147 | EAS | JPT | ARSF_chrX_3036471_3117727 | ARSF | chrX | 3036471 | 3117727 |
NA19004 | hp1 | a0001 | c0001 | t0001 | g0111 | EAS | JPT | ARSF_chrX_3036471_3117727 | ARSF | chrX | 3036471 | 3117727 |
NA19005 | hp1 | a0001 | c0001 | t0001 | g0070 | EAS | JPT | ARSF_chrX_3036471_3117727 | ARSF | chrX | 3036471 | 3117727 |
NA19007 | hp1 | a0001 | c0001 | t0001 | g0152 | EAS | JPT | ARSF_chrX_3036471_3117727 | ARSF | chrX | 3036471 | 3117727 |
NA19009 | hp1 | a0001 | c0001 | t0004 | g0113 | EAS | JPT | ARSF_chrX_3036471_3117727 | ARSF | chrX | 3036471 | 3117727 |
NA19012 | hp1 | a0001 | c0001 | t0001 | g0165 | EAS | JPT | ARSF_chrX_3036471_3117727 | ARSF | chrX | 3036471 | 3117727 |
NA19030 | hp1 | a0001 | c0012 | t0001 | g0089 | AFR | LWK | ARSF_chrX_3036471_3117727 | ARSF | chrX | 3036471 | 3117727 |
NA19030 | hp2 | a0003 | c0013 | t0001 | g0098 | AFR | LWK | ARSF_chrX_3036471_3117727 | ARSF | chrX | 3036471 | 3117727 |
NA19043 | hp1 | a0001 | c0001 | t0001 | g0011 | AFR | LWK | ARSF_chrX_3036471_3117727 | ARSF | chrX | 3036471 | 3117727 |
NA19056 | hp1 | a0001 | c0001 | t0005 | g0077 | EAS | JPT | ARSF_chrX_3036471_3117727 | ARSF | chrX | 3036471 | 3117727 |
NA19058 | hp1 | a0001 | c0001 | t0001 | g0123 | EAS | JPT | ARSF_chrX_3036471_3117727 | ARSF | chrX | 3036471 | 3117727 |
NA19060 | hp1 | a0001 | c0002 | t0001 | g0067 | EAS | JPT | ARSF_chrX_3036471_3117727 | ARSF | chrX | 3036471 | 3117727 |
NA19063 | hp1 | a0001 | c0001 | t0001 | g0186 | EAS | JPT | ARSF_chrX_3036471_3117727 | ARSF | chrX | 3036471 | 3117727 |
NA19066 | hp1 | a0001 | c0001 | t0001 | g0158 | EAS | JPT | ARSF_chrX_3036471_3117727 | ARSF | chrX | 3036471 | 3117727 |
NA19068 | hp1 | a0001 | c0001 | t0001 | g0068 | EAS | JPT | ARSF_chrX_3036471_3117727 | ARSF | chrX | 3036471 | 3117727 |
NA19070 | hp1 | a0001 | c0001 | t0001 | g0080 | EAS | JPT | ARSF_chrX_3036471_3117727 | ARSF | chrX | 3036471 | 3117727 |
NA19072 | hp1 | a0001 | c0001 | t0001 | g0056 | EAS | JPT | ARSF_chrX_3036471_3117727 | ARSF | chrX | 3036471 | 3117727 |
NA19074 | hp1 | a0001 | c0001 | t0001 | g0046 | EAS | JPT | ARSF_chrX_3036471_3117727 | ARSF | chrX | 3036471 | 3117727 |
NA19074 | hp2 | a0001 | c0001 | t0001 | g0076 | EAS | JPT | ARSF_chrX_3036471_3117727 | ARSF | chrX | 3036471 | 3117727 |
NA19076 | hp1 | a0001 | c0001 | t0001 | g0073 | EAS | JPT | ARSF_chrX_3036471_3117727 | ARSF | chrX | 3036471 | 3117727 |
NA19079 | hp1 | a0001 | c0001 | t0001 | g0156 | EAS | JPT | ARSF_chrX_3036471_3117727 | ARSF | chrX | 3036471 | 3117727 |
NA19082 | hp1 | a0001 | c0001 | t0001 | g0120 | EAS | JPT | ARSF_chrX_3036471_3117727 | ARSF | chrX | 3036471 | 3117727 |
NA19083 | hp1 | a0001 | c0001 | t0001 | g0075 | EAS | JPT | ARSF_chrX_3036471_3117727 | ARSF | chrX | 3036471 | 3117727 |
NA19085 | hp1 | a0001 | c0001 | t0001 | g0108 | EAS | JPT | ARSF_chrX_3036471_3117727 | ARSF | chrX | 3036471 | 3117727 |
NA19086 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | ARSF_chrX_3036471_3117727 | ARSF | chrX | 3036471 | 3117727 |
NA19088 | hp1 | a0001 | c0001 | t0001 | g0178 | EAS | JPT | ARSF_chrX_3036471_3117727 | ARSF | chrX | 3036471 | 3117727 |
NA19089 | hp1 | a0001 | c0001 | t0001 | g0175 | EAS | JPT | ARSF_chrX_3036471_3117727 | ARSF | chrX | 3036471 | 3117727 |
NA19091 | hp1 | a0001 | c0001 | t0001 | g0137 | EAS | JPT | ARSF_chrX_3036471_3117727 | ARSF | chrX | 3036471 | 3117727 |
NA19240 | hp1 | a0001 | c0001 | t0001 | g0032 | AFR | YRI | ARSF_chrX_3036471_3117727 | ARSF | chrX | 3036471 | 3117727 |
NA19240 | hp2 | a0001 | c0002 | t0001 | g0022 | AFR | YRI | ARSF_chrX_3036471_3117727 | ARSF | chrX | 3036471 | 3117727 |
NA20129 | hp1 | a0005 | c0011 | t0001 | g0034 | AFR | ASW | ARSF_chrX_3036471_3117727 | ARSF | chrX | 3036471 | 3117727 |
NA20129 | hp2 | a0001 | c0005 | t0001 | g0010 | AFR | ASW | ARSF_chrX_3036471_3117727 | ARSF | chrX | 3036471 | 3117727 |
NA20752 | hp1 | a0001 | c0001 | t0001 | g0091 | EUR | TSI | ARSF_chrX_3036471_3117727 | ARSF | chrX | 3036471 | 3117727 |
NA20805 | hp1 | a0001 | c0001 | t0001 | g0060 | EUR | TSI | ARSF_chrX_3036471_3117727 | ARSF | chrX | 3036471 | 3117727 |
NA20905 | hp1 | a0001 | c0001 | t0001 | g0146 | SAS | GIH | ARSF_chrX_3036471_3117727 | ARSF | chrX | 3036471 | 3117727 |
HG02486 | hp1 | a0001 | c0001 | t0001 | g0006 | AFR | ACB | ARSF_chrX_3036471_3117727 | ARSF | chrX | 3036471 | 3117727 |
HG03471 | hp1 | a0001 | c0001 | t0001 | g0168 | AFR | MSL | ARSF_chrX_3036471_3117727 | ARSF | chrX | 3036471 | 3117727 |
NA18955 | hp1 | a0001 | c0001 | t0001 | g0107 | EAS | JPT | ARSF_chrX_3036471_3117727 | ARSF | chrX | 3036471 | 3117727 |
NA21309 | hp1 | a0004 | c0006 | t0001 | g0130 | AFR | LWK | ARSF_chrX_3036471_3117727 | ARSF | chrX | 3036471 | 3117727 |
NA21309 | hp2 | a0001 | c0001 | t0001 | g0035 | AFR | LWK | ARSF_chrX_3036471_3117727 | ARSF | chrX | 3036471 | 3117727 |
homoSapiens | chm13v2 | a0001 | c0002 | t0001 | g0029 | REF | REF | ARSF_chrX_3036471_3117727 | ARSF | chrX | 3036471 | 3117727 |
homoSapiens | grch38p0 | a0001 | c0002 | t0001 | g0023 | REF | REF | ARSF_chrX_3036471_3117727 | ARSF | chrX | 3036471 | 3117727 |
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:3081002 | C | T | 1 | a0005 | 3 | HG02572.hp1 HG03041.hp2 NA20129.hp1 |
missense_variant | MODERATE | c.395C>T | p.Thr132Met | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 5/11 | 616/2165 | 395/1773 | 132/590 | chrX | 3081002 | |||
chrX:3084428 | A | T | 1 | a0007 | 1 | HG00597.hp1 | missense_variant | MODERATE | c.592A>T | p.Ile198Phe | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 6/11 | 813/2165 | 592/1773 | 198/590 | chrX | 3084428 | |||
chrX:3084434 | A | G | 1 | a0004 | 3 | HG01168.hp1 HG01169.hp2 NA21309.hp1 |
missense_variant | MODERATE | c.598A>G | p.Ile200Val | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 6/11 | 819/2165 | 598/1773 | 200/590 | chrX | 3084434 | |||
chrX:3084485 | C | T | 1 | a0008 | 1 | HG00673.hp1 | missense_variant | MODERATE | c.649C>T | p.Leu217Phe | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 6/11 | 870/2165 | 649/1773 | 217/590 | chrX | 3084485 | |||
chrX:3101123 | G | A | 1 | a0003 | 4 | HG01074.hp1 HG02258.hp1 HG03139.hp1 others(1): Show |
missense_variant | MODERATE | c.1004G>A | p.Arg335Lys | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 8/11 | 1225/2165 | 1004/1773 | 335/590 | chrX | 3101123 | |||
chrX:3103777 | G | A | 1 | a0007 | 1 | HG00597.hp1 | missense_variant | MODERATE | c.1118G>A | p.Gly373Glu | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 9/11 | 1339/2165 | 1118/1773 | 373/590 | chrX | 3103777 | |||
chrX:3112362 | C | T | 2 | a0002 a0007 |
10 | HG00099.hp2 HG00597.hp1 HG01070.hp1 others(7): Show |
missense_variant | MODERATE | c.1579C>T | p.His527Tyr | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 11/11 | 1800/2165 | 1579/1773 | 527/590 | chrX | 3112362 |
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:3084280 | T | C | 1 | a0001c0012 | 1 | NA19030.hp1 | synonymous_variant | LOW | c.444T>C | p.Ser148Ser | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 6/11 | 665/2165 | 444/1773 | 148/590 | chrX | 3084280 | |||
chrX:3084472 | C | A | 1 | a0003c0013 | 1 | NA19030.hp2 | synonymous_variant | LOW | c.636C>A | p.Val212Val | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 6/11 | 857/2165 | 636/1773 | 212/590 | chrX | 3084472 | |||
chrX:3084646 | A | G | 14 | a0001c0001 a0001c0005 a0001c0009 others(11): Show |
166 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(163): Show |
synonymous_variant | LOW | c.810A>G | p.Glu270Glu | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 6/11 | 1031/2165 | 810/1773 | 270/590 | chrX | 3084646 | |||
chrX:3101106 | C | T | 2 | a0001c0007 a0001c0010 |
4 | HG02257.hp2 HG02280.hp1 HG02809.hp1 others(1): Show |
synonymous_variant | LOW | c.987C>T | p.Ile329Ile | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 8/11 | 1208/2165 | 987/1773 | 329/590 | chrX | 3101106 | |||
chrX:3110219 | C | T | 9 | a0001c0005 a0001c0015 a0001c0016 others(6): Show |
15 | HG01074.hp1 HG01168.hp1 HG01169.hp2 others(12): Show |
synonymous_variant | LOW | c.1357C>T | p.Leu453Leu | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 10/11 | 1578/2165 | 1357/1773 | 453/590 | chrX | 3110219 | |||
chrX:3110248 | C | T | 9 | a0001c0005 a0001c0015 a0001c0016 others(6): Show |
15 | HG01074.hp1 HG01168.hp1 HG01169.hp2 others(12): Show |
synonymous_variant | LOW | c.1386C>T | p.Asp462Asp | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 10/11 | 1607/2165 | 1386/1773 | 462/590 | chrX | 3110248 | |||
chrX:3112385 | G | A | 4 | a0001c0015 a0001c0019 a0003c0017 others(1): Show |
6 | HG01074.hp1 HG01168.hp1 HG01169.hp2 others(3): Show |
synonymous_variant | LOW | c.1602G>A | p.Val534Val | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 11/11 | 1823/2165 | 1602/1773 | 534/590 | chrX | 3112385 |
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:3112535 | G | GGGTCCTA others(43): Show |
1 | a0001c0009t0001 | 2 | HG03491.hp1 HG03492.hp1 |
3_prime_UTR_variant | MODIFIER | c.*18_*67dupGAGGAAGC others(42): Show |
ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 11/11 | 68 | INFO_REALIGN_3_PRIME | chrX | 3112535 | |||||
chrX:3112535 | GGGTCCTA others(43): Show |
G | 2 | a0006c0014t0002 a0006c0018t0002 |
2 | HG01884.hp1 HG02451.hp2 |
3_prime_UTR_variant | MODIFIER | c.*18_*67delGAGGAAGC others(42): Show |
ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 11/11 | 18 | INFO_REALIGN_3_PRIME | chrX | 3112535 | |||||
chrX:3112574 | G | GAGGAAGC others(43): Show |
1 | a0001c0015t0006 | 1 | HG03239.hp2 | 3_prime_UTR_variant | MODIFIER | c.*26_*75dupCTTTGGTC others(42): Show |
ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 11/11 | 76 | INFO_REALIGN_3_PRIME | chrX | 3112574 | |||||
chrX:3112594 | C | A | 1 | a0001c0001t0004 | 1 | NA19009.hp1 | 3_prime_UTR_variant | MODIFIER | c.*38C>A | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 11/11 | 38 | chrX | 3112594 | ||||||
chrX:3112654 | T | G | 1 | a0001c0001t0005 | 1 | NA19056.hp1 | 3_prime_UTR_variant | MODIFIER | c.*98T>G | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 11/11 | 98 | chrX | 3112654 | ||||||
chrX:3112719 | G | T | 1 | a0001c0007t0003 | 2 | HG02257.hp2 HG02965.hp1 |
3_prime_UTR_variant | MODIFIER | c.*163G>T | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 11/11 | 163 | chrX | 3112719 |
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:3041820 | C | T | 149 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(146): Show |
156 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(153): Show |
intron_variant | MODIFIER | c.-29+157C>T | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 1/10 | chrX | 3041820 | |||||||
chrX:3042175 | A | T | 3 | a0001c0001t0001g0044 a0001c0005t0001g0042 a0001c0005t0001g0043 |
3 | HG01884.hp2 HG02922.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.-29+512A>T | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 1/10 | chrX | 3042175 | |||||||
chrX:3042319 | G | C | 2 | a0004c0006t0001g0008 a0004c0006t0001g0009 |
2 | HG01168.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.-29+656G>C | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 1/10 | chrX | 3042319 | |||||||
chrX:3042420 | AAATTG | A | 2 | a0004c0006t0001g0008 a0004c0006t0001g0009 |
2 | HG01168.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.-29+758_-29+762del others(5): Show |
ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 1/10 | chrX | 3042420 | |||||||
chrX:3042440 | T | G | 1 | a0001c0001t0001g0045 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.-29+777T>G | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 1/10 | chrX | 3042440 | |||||||
chrX:3042476 | A | C | 1 | a0001c0001t0001g0186 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.-29+813A>C | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 1/10 | chrX | 3042476 | |||||||
chrX:3042619 | C | A | 1 | a0001c0001t0001g0046 | 1 | NA19074.hp1 | intron_variant | MODIFIER | c.-29+956C>A | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 1/10 | chrX | 3042619 | |||||||
chrX:3042880 | C | T | 9 | a0001c0001t0001g0035 a0001c0001t0001g0036 a0001c0001t0001g0037 others(6): Show |
9 | HG02280.hp1 HG02451.hp1 HG02809.hp1 others(6): Show |
intron_variant | MODIFIER | c.-29+1217C>T | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 1/10 | chrX | 3042880 | |||||||
chrX:3043277 | A | C | 2 | a0004c0006t0001g0008 a0004c0006t0001g0009 |
2 | HG01168.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.-29+1614A>C | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 1/10 | chrX | 3043277 | |||||||
chrX:3043564 | C | T | 9 | a0001c0001t0001g0035 a0001c0001t0001g0036 a0001c0001t0001g0037 others(6): Show |
9 | HG02280.hp1 HG02451.hp1 HG02809.hp1 others(6): Show |
intron_variant | MODIFIER | c.-29+1901C>T | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 1/10 | chrX | 3043564 | |||||||
chrX:3043584 | C | T | 1 | a0001c0001t0001g0032 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.-29+1921C>T | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 1/10 | chrX | 3043584 | |||||||
chrX:3043610 | G | C | 9 | a0001c0001t0001g0035 a0001c0001t0001g0036 a0001c0001t0001g0037 others(6): Show |
9 | HG02280.hp1 HG02451.hp1 HG02809.hp1 others(6): Show |
intron_variant | MODIFIER | c.-29+1947G>C | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 1/10 | chrX | 3043610 | |||||||
chrX:3043658 | T | C | 150 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(147): Show |
157 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(154): Show |
intron_variant | MODIFIER | c.-29+1995T>C | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 1/10 | chrX | 3043658 | |||||||
chrX:3043771 | CTGTT | C | 4 | a0001c0001t0001g0001 a0001c0001t0001g0047 a0001c0001t0001g0048 others(1): Show |
5 | HG00738.hp1 HG01256.hp1 HG01952.hp1 others(2): Show |
intron_variant | MODIFIER | c.-29+2115_-29+2118d others(6): Show |
ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chrX | 3043771 | ||||||
chrX:3043794 | A | T | 1 | a0001c0001t0001g0186 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.-29+2131A>T | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 1/10 | chrX | 3043794 | |||||||
chrX:3043851 | G | T | 156 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(153): Show |
163 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(160): Show |
intron_variant | MODIFIER | c.-29+2188G>T | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 1/10 | chrX | 3043851 | |||||||
chrX:3044070 | T | C | 168 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(165): Show |
175 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(172): Show |
intron_variant | MODIFIER | c.-29+2407T>C | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 1/10 | chrX | 3044070 | |||||||
chrX:3044178 | A | G | 2 | a0004c0006t0001g0008 a0004c0006t0001g0009 |
2 | HG01168.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.-29+2515A>G | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 1/10 | chrX | 3044178 | |||||||
chrX:3044416 | T | C | 150 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(147): Show |
157 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(154): Show |
intron_variant | MODIFIER | c.-29+2753T>C | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 1/10 | chrX | 3044416 | |||||||
chrX:3044444 | T | C | 2 | a0004c0006t0001g0008 a0004c0006t0001g0009 |
2 | HG01168.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.-29+2781T>C | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 1/10 | chrX | 3044444 | |||||||
chrX:3044461 | C | G | 1 | a0001c0001t0001g0178 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.-29+2798C>G | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 1/10 | chrX | 3044461 | |||||||
chrX:3044580 | G | A | 2 | a0004c0006t0001g0008 a0004c0006t0001g0009 |
2 | HG01168.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.-29+2917G>A | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 1/10 | chrX | 3044580 | |||||||
chrX:3044665 | A | C | 1 | a0001c0001t0001g0044 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.-29+3002A>C | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 1/10 | chrX | 3044665 | |||||||
chrX:3044666 | T | A | 156 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(153): Show |
163 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(160): Show |
intron_variant | MODIFIER | c.-29+3003T>A | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 1/10 | chrX | 3044666 | |||||||
chrX:3044771 | G | A | 12 | a0001c0001t0001g0032 a0001c0001t0001g0035 a0001c0001t0001g0036 others(9): Show |
12 | HG01070.hp1 HG01071.hp2 HG02280.hp1 others(9): Show |
intron_variant | MODIFIER | c.-29+3108G>A | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 1/10 | chrX | 3044771 | |||||||
chrX:3045554 | CT | C | 14 | a0001c0001t0001g0051 a0001c0001t0001g0052 a0001c0001t0001g0053 others(11): Show |
14 | HG00735.hp1 HG01070.hp1 HG01071.hp2 others(11): Show |
intron_variant | MODIFIER | c.-29+3909delT | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chrX | 3045554 | ||||||
chrX:3045568 | T | C | 1 | a0002c0003t0001g0050 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.-29+3905T>C | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 1/10 | chrX | 3045568 | |||||||
chrX:3045642 | A | G | 148 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(145): Show |
155 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(152): Show |
intron_variant | MODIFIER | c.-29+3979A>G | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 1/10 | chrX | 3045642 | |||||||
chrX:3045649 | G | A | 2 | a0004c0006t0001g0008 a0004c0006t0001g0009 |
2 | HG01168.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.-29+3986G>A | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 1/10 | chrX | 3045649 | |||||||
chrX:3045712 | C | T | 148 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(145): Show |
155 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(152): Show |
intron_variant | MODIFIER | c.-29+4049C>T | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 1/10 | chrX | 3045712 | |||||||
chrX:3045713 | A | G | 148 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(145): Show |
155 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(152): Show |
intron_variant | MODIFIER | c.-29+4050A>G | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 1/10 | chrX | 3045713 | |||||||
chrX:3045716 | T | C | 147 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(144): Show |
154 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(151): Show |
intron_variant | MODIFIER | c.-29+4053T>C | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 1/10 | chrX | 3045716 | |||||||
chrX:3045853 | GC | G | 4 | a0001c0001t0001g0057 a0001c0001t0001g0058 a0001c0001t0001g0059 others(1): Show |
4 | HG01069.hp1 HG01071.hp1 HG01358.hp1 others(1): Show |
intron_variant | MODIFIER | c.-29+4192delC | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chrX | 3045853 | ||||||
chrX:3045869 | TTTTTGTT others(2): Show |
T | 6 | a0001c0002t0001g0181 a0001c0002t0001g0183 a0001c0002t0001g0184 others(3): Show |
6 | HG01109.hp1 HG02257.hp2 HG02622.hp2 others(3): Show |
intron_variant | MODIFIER | c.-29+4215_-29+4223d others(11): Show |
ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chrX | 3045869 | ||||||
chrX:3045944 | G | A | 148 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(145): Show |
155 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(152): Show |
intron_variant | MODIFIER | c.-29+4281G>A | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 1/10 | chrX | 3045944 | |||||||
chrX:3046133 | G | A | 148 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(145): Show |
155 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(152): Show |
intron_variant | MODIFIER | c.-29+4470G>A | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 1/10 | chrX | 3046133 | |||||||
chrX:3046205 | C | T | 3 | a0001c0002t0001g0014 a0001c0002t0001g0028 a0001c0002t0001g0030 |
3 | HG00642.hp1 HG00735.hp1 HG03688.hp1 |
intron_variant | MODIFIER | c.-29+4542C>T | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 1/10 | chrX | 3046205 | |||||||
chrX:3046301 | C | T | 1 | a0001c0001t0001g0177 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.-29+4638C>T | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 1/10 | chrX | 3046301 | |||||||
chrX:3046442 | G | A | 2 | a0002c0004t0001g0179 a0002c0004t0001g0180 |
2 | HG01070.hp1 HG01071.hp2 |
intron_variant | MODIFIER | c.-29+4779G>A | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 1/10 | chrX | 3046442 | |||||||
chrX:3046705 | G | C | 3 | a0001c0001t0001g0061 a0001c0001t0001g0062 a0001c0001t0001g0063 |
3 | HG00323.hp2 HG01106.hp1 HG01496.hp1 |
intron_variant | MODIFIER | c.-29+5042G>C | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 1/10 | chrX | 3046705 | |||||||
chrX:3046802 | A | G | 1 | a0001c0001t0001g0176 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.-29+5139A>G | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 1/10 | chrX | 3046802 | |||||||
chrX:3047008 | A | G | 2 | a0001c0001t0001g0007 a0001c0001t0001g0175 |
3 | NA18951.hp1 NA18994.hp1 NA19089.hp1 |
intron_variant | MODIFIER | c.-29+5345A>G | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 1/10 | chrX | 3047008 | |||||||
chrX:3047041 | A | G | 169 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(166): Show |
176 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(173): Show |
intron_variant | MODIFIER | c.-29+5378A>G | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 1/10 | chrX | 3047041 | |||||||
chrX:3047125 | T | C | 161 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(158): Show |
168 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(165): Show |
intron_variant | MODIFIER | c.-29+5462T>C | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 1/10 | chrX | 3047125 | |||||||
chrX:3047183 | AT | A | 11 | a0001c0001t0001g0035 a0001c0001t0001g0036 a0001c0001t0001g0037 others(8): Show |
11 | HG01069.hp1 HG02280.hp1 HG02451.hp1 others(8): Show |
intron_variant | MODIFIER | c.-29+5533delT | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chrX | 3047183 | ||||||
chrX:3047476 | A | AG | 149 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(146): Show |
156 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(153): Show |
intron_variant | MODIFIER | c.-29+5813_-29+5814i others(3): Show |
ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 1/10 | chrX | 3047476 | |||||||
chrX:3047481 | T | G | 149 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(146): Show |
156 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(153): Show |
intron_variant | MODIFIER | c.-29+5818T>G | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 1/10 | chrX | 3047481 | |||||||
chrX:3047485 | C | T | 149 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(146): Show |
156 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(153): Show |
intron_variant | MODIFIER | c.-29+5822C>T | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 1/10 | chrX | 3047485 | |||||||
chrX:3047773 | C | T | 2 | a0004c0006t0001g0008 a0004c0006t0001g0009 |
2 | HG01168.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.-29+6110C>T | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 1/10 | chrX | 3047773 | |||||||
chrX:3047840 | G | A | 149 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(146): Show |
156 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(153): Show |
intron_variant | MODIFIER | c.-29+6177G>A | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 1/10 | chrX | 3047840 | |||||||
chrX:3047844 | T | C | 149 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(146): Show |
156 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(153): Show |
intron_variant | MODIFIER | c.-29+6181T>C | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 1/10 | chrX | 3047844 | |||||||
chrX:3047892 | C | T | 1 | a0001c0001t0001g0041 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.-29+6229C>T | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 1/10 | chrX | 3047892 | |||||||
chrX:3047905 | T | C | 149 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(146): Show |
156 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(153): Show |
intron_variant | MODIFIER | c.-29+6242T>C | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 1/10 | chrX | 3047905 | |||||||
chrX:3047981 | A | G | 150 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(147): Show |
157 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(154): Show |
intron_variant | MODIFIER | c.-29+6318A>G | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 1/10 | chrX | 3047981 | |||||||
chrX:3048180 | C | T | 149 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(146): Show |
156 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(153): Show |
intron_variant | MODIFIER | c.-29+6517C>T | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 1/10 | chrX | 3048180 | |||||||
chrX:3048208 | T | A | 149 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(146): Show |
156 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(153): Show |
intron_variant | MODIFIER | c.-29+6545T>A | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 1/10 | chrX | 3048208 | |||||||
chrX:3048376 | G | A | 1 | a0005c0011t0001g0027 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.-29+6713G>A | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 1/10 | chrX | 3048376 | |||||||
chrX:3048417 | G | A | 1 | a0005c0011t0001g0027 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.-29+6754G>A | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 1/10 | chrX | 3048417 | |||||||
chrX:3048441 | T | C | 149 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(146): Show |
156 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(153): Show |
intron_variant | MODIFIER | c.-29+6778T>C | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 1/10 | chrX | 3048441 | |||||||
chrX:3048745 | A | G | 1 | a0005c0011t0001g0027 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.-29+7082A>G | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 1/10 | chrX | 3048745 | |||||||
chrX:3048900 | C | T | 3 | a0001c0001t0001g0064 a0001c0001t0001g0172 a0001c0001t0001g0173 |
3 | HG02135.hp1 NA18986.hp1 NA18998.hp2 |
intron_variant | MODIFIER | c.-29+7237C>T | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 1/10 | chrX | 3048900 | |||||||
chrX:3048965 | T | A | 149 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(146): Show |
156 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(153): Show |
intron_variant | MODIFIER | c.-29+7302T>A | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 1/10 | chrX | 3048965 | |||||||
chrX:3049015 | A | G | 148 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(145): Show |
155 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(152): Show |
intron_variant | MODIFIER | c.-29+7352A>G | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 1/10 | chrX | 3049015 | |||||||
chrX:3049082 | G | T | 1 | a0001c0001t0001g0171 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.-29+7419G>T | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 1/10 | chrX | 3049082 | |||||||
chrX:3049096 | G | A | 176 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(173): Show |
183 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(180): Show |
intron_variant | MODIFIER | c.-29+7433G>A | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 1/10 | chrX | 3049096 | |||||||
chrX:3049135 | A | G | 149 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(146): Show |
156 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(153): Show |
intron_variant | MODIFIER | c.-29+7472A>G | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 1/10 | chrX | 3049135 | |||||||
chrX:3049145 | C | T | 1 | a0001c0001t0001g0171 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.-29+7482C>T | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 1/10 | chrX | 3049145 | |||||||
chrX:3049211 | T | C | 5 | a0001c0001t0001g0035 a0001c0001t0001g0041 a0001c0010t0001g0033 others(2): Show |
5 | HG02280.hp1 HG02809.hp1 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.-29+7548T>C | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 1/10 | chrX | 3049211 | |||||||
chrX:3049331 | C | T | 6 | a0001c0002t0001g0181 a0001c0002t0001g0183 a0001c0002t0001g0184 others(3): Show |
6 | HG01109.hp1 HG02257.hp2 HG02622.hp2 others(3): Show |
intron_variant | MODIFIER | c.-29+7668C>T | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 1/10 | chrX | 3049331 | |||||||
chrX:3049397 | A | T | 1 | a0005c0011t0001g0027 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.-29+7734A>T | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 1/10 | chrX | 3049397 | |||||||
chrX:3049659 | A | G | 149 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(146): Show |
156 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(153): Show |
intron_variant | MODIFIER | c.-29+7996A>G | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 1/10 | chrX | 3049659 | |||||||
chrX:3049929 | T | C | 158 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(155): Show |
165 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(162): Show |
intron_variant | MODIFIER | c.-29+8266T>C | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 1/10 | chrX | 3049929 | |||||||
chrX:3050027 | T | G | 1 | a0001c0001t0001g0032 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.-29+8364T>G | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 1/10 | chrX | 3050027 | |||||||
chrX:3050069 | G | C | 158 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(155): Show |
165 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(162): Show |
intron_variant | MODIFIER | c.-29+8406G>C | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 1/10 | chrX | 3050069 | |||||||
chrX:3050143 | T | A | 2 | a0001c0001t0001g0051 a0001c0001t0001g0065 |
2 | HG02647.hp1 HG02896.hp1 |
intron_variant | MODIFIER | c.-29+8480T>A | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 1/10 | chrX | 3050143 | |||||||
chrX:3050271 | T | C | 8 | a0001c0002t0001g0181 a0001c0002t0001g0183 a0001c0002t0001g0184 others(5): Show |
8 | HG01070.hp1 HG01071.hp2 HG01109.hp1 others(5): Show |
intron_variant | MODIFIER | c.-29+8608T>C | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 1/10 | chrX | 3050271 | |||||||
chrX:3050391 | G | A | 158 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(155): Show |
165 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(162): Show |
intron_variant | MODIFIER | c.-29+8728G>A | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 1/10 | chrX | 3050391 | |||||||
chrX:3050407 | G | A | 2 | a0004c0006t0001g0008 a0004c0006t0001g0009 |
2 | HG01168.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.-29+8744G>A | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 1/10 | chrX | 3050407 | |||||||
chrX:3050546 | C | CA | 24 | a0001c0001t0001g0047 a0001c0001t0001g0066 a0001c0001t0001g0068 others(21): Show |
24 | HG00738.hp1 HG01070.hp1 HG01071.hp2 others(21): Show |
intron_variant | MODIFIER | c.-29+8900dupA | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chrX | 3050546 | ||||||
chrX:3050546 | CA | C | 6 | a0001c0001t0001g0056 a0001c0001t0001g0168 a0001c0001t0001g0170 others(3): Show |
6 | HG02602.hp1 HG03041.hp1 HG03041.hp2 others(3): Show |
intron_variant | MODIFIER | c.-29+8900delA | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chrX | 3050546 | ||||||
chrX:3050607 | T | C | 158 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(155): Show |
165 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(162): Show |
intron_variant | MODIFIER | c.-29+8944T>C | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 1/10 | chrX | 3050607 | |||||||
chrX:3050687 | G | C | 8 | a0001c0002t0001g0181 a0001c0002t0001g0183 a0001c0002t0001g0184 others(5): Show |
8 | HG01070.hp1 HG01071.hp2 HG01109.hp1 others(5): Show |
intron_variant | MODIFIER | c.-29+9024G>C | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 1/10 | chrX | 3050687 | |||||||
chrX:3050874 | G | T | 158 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(155): Show |
165 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(162): Show |
intron_variant | MODIFIER | c.-29+9211G>T | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 1/10 | chrX | 3050874 | |||||||
chrX:3050902 | C | T | 1 | a0001c0002t0001g0030 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.-29+9239C>T | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 1/10 | chrX | 3050902 | |||||||
chrX:3050917 | C | T | 148 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(145): Show |
155 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(152): Show |
intron_variant | MODIFIER | c.-29+9254C>T | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 1/10 | chrX | 3050917 | |||||||
chrX:3050979 | C | T | 1 | a0005c0011t0001g0027 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.-29+9316C>T | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 1/10 | chrX | 3050979 | |||||||
chrX:3051026 | C | T | 2 | a0001c0001t0001g0165 a0001c0001t0001g0166 |
2 | NA19000.hp1 NA19012.hp1 |
intron_variant | MODIFIER | c.-29+9363C>T | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 1/10 | chrX | 3051026 | |||||||
chrX:3051194 | C | A | 1 | a0001c0001t0001g0171 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.-29+9531C>A | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 1/10 | chrX | 3051194 | |||||||
chrX:3051207 | C | A | 1 | a0002c0003t0001g0050 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.-29+9544C>A | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 1/10 | chrX | 3051207 | |||||||
chrX:3051489 | T | C | 9 | a0001c0001t0001g0046 a0001c0001t0001g0081 a0001c0001t0001g0082 others(6): Show |
9 | HG02071.hp1 NA18612.hp1 NA18952.hp1 others(6): Show |
intron_variant | MODIFIER | c.-29+9826T>C | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 1/10 | chrX | 3051489 | |||||||
chrX:3051497 | C | T | 1 | a0001c0001t0001g0063 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.-29+9834C>T | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 1/10 | chrX | 3051497 | |||||||
chrX:3051498 | G | A | 14 | a0001c0001t0001g0032 a0001c0001t0001g0035 a0001c0001t0001g0036 others(11): Show |
14 | HG01168.hp1 HG01169.hp2 HG02280.hp1 others(11): Show |
intron_variant | MODIFIER | c.-29+9835G>A | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 1/10 | chrX | 3051498 | |||||||
chrX:3051590 | C | CTA | 23 | a0001c0001t0001g0032 a0001c0001t0001g0035 a0001c0001t0001g0036 others(20): Show |
23 | HG01070.hp1 HG01071.hp2 HG01109.hp1 others(20): Show |
intron_variant | MODIFIER | c.-29+9928_-29+9929i others(4): Show |
ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chrX | 3051590 | ||||||
chrX:3051883 | C | T | 9 | a0001c0002t0001g0181 a0001c0002t0001g0183 a0001c0002t0001g0184 others(6): Show |
9 | HG01070.hp1 HG01071.hp2 HG01109.hp1 others(6): Show |
intron_variant | MODIFIER | c.-29+10220C>T | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 1/10 | chrX | 3051883 | |||||||
chrX:3051905 | A | G | 1 | a0001c0001t0001g0164 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.-29+10242A>G | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 1/10 | chrX | 3051905 | |||||||
chrX:3051995 | A | G | 1 | a0001c0001t0001g0163 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.-29+10332A>G | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 1/10 | chrX | 3051995 | |||||||
chrX:3052028 | C | CA | 5 | a0001c0001t0001g0032 a0001c0001t0001g0056 a0001c0001t0001g0081 others(2): Show |
5 | HG02572.hp1 NA18961.hp1 NA19030.hp1 others(2): Show |
intron_variant | MODIFIER | c.-29+10374dupA | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chrX | 3052028 | ||||||
chrX:3052133 | G | A | 1 | a0001c0001t0001g0091 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.-29+10470G>A | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 1/10 | chrX | 3052133 | |||||||
chrX:3052181 | G | A | 1 | a0001c0001t0001g0046 | 1 | NA19074.hp1 | intron_variant | MODIFIER | c.-29+10518G>A | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 1/10 | chrX | 3052181 | |||||||
chrX:3052302 | T | C | 5 | a0001c0001t0001g0032 a0001c0012t0001g0089 a0004c0006t0001g0008 others(2): Show |
5 | HG01168.hp1 HG01169.hp2 HG02572.hp1 others(2): Show |
intron_variant | MODIFIER | c.-29+10639T>C | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 1/10 | chrX | 3052302 | |||||||
chrX:3052690 | C | CA | 9 | a0001c0002t0001g0181 a0001c0002t0001g0183 a0001c0002t0001g0184 others(6): Show |
9 | HG01070.hp1 HG01071.hp2 HG01109.hp1 others(6): Show |
intron_variant | MODIFIER | c.-29+11044dupA | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chrX | 3052690 | ||||||
chrX:3052690 | C | CAA | 11 | a0001c0001t0001g0035 a0001c0001t0001g0036 a0001c0001t0001g0037 others(8): Show |
11 | HG01168.hp1 HG01169.hp2 HG02280.hp1 others(8): Show |
intron_variant | MODIFIER | c.-29+11043_-29+1104 others(6): Show |
ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chrX | 3052690 | ||||||
chrX:3052690 | CA | C | 143 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(140): Show |
150 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(147): Show |
intron_variant | MODIFIER | c.-29+11044delA | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chrX | 3052690 | ||||||
chrX:3052690 | CAA | C | 5 | a0001c0001t0001g0055 a0001c0001t0001g0057 a0001c0001t0001g0080 others(2): Show |
5 | HG01069.hp1 HG01934.hp1 HG01943.hp1 others(2): Show |
intron_variant | MODIFIER | c.-29+11043_-29+1104 others(6): Show |
ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chrX | 3052690 | ||||||
chrX:3053075 | C | T | 2 | a0001c0001t0001g0032 a0001c0012t0001g0089 |
2 | NA19030.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.-29+11412C>T | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 1/10 | chrX | 3053075 | |||||||
chrX:3053328 | C | CT | 8 | a0001c0001t0001g0032 a0001c0001t0001g0081 a0001c0001t0001g0157 others(5): Show |
8 | HG00609.hp1 HG01192.hp1 HG02055.hp1 others(5): Show |
intron_variant | MODIFIER | c.-29+11685dupT | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chrX | 3053328 | ||||||
chrX:3053328 | CT | C | 14 | a0001c0001t0001g0036 a0001c0001t0001g0037 a0001c0001t0001g0038 others(11): Show |
14 | HG00280.hp1 HG01167.hp1 HG01168.hp1 others(11): Show |
intron_variant | MODIFIER | c.-29+11685delT | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chrX | 3053328 | ||||||
chrX:3053328 | CTTTT | C | 9 | a0001c0002t0001g0181 a0001c0002t0001g0183 a0001c0002t0001g0184 others(6): Show |
9 | HG01070.hp1 HG01071.hp2 HG01109.hp1 others(6): Show |
intron_variant | MODIFIER | c.-29+11682_-29+1168 others(8): Show |
ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chrX | 3053328 | ||||||
chrX:3053410 | A | C | 168 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(165): Show |
175 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(172): Show |
intron_variant | MODIFIER | c.-29+11747A>C | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 1/10 | chrX | 3053410 | |||||||
chrX:3053639 | C | T | 167 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(164): Show |
174 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(171): Show |
intron_variant | MODIFIER | c.-29+11976C>T | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 1/10 | chrX | 3053639 | |||||||
chrX:3053667 | T | C | 9 | a0001c0002t0001g0181 a0001c0002t0001g0183 a0001c0002t0001g0184 others(6): Show |
9 | HG01070.hp1 HG01071.hp2 HG01109.hp1 others(6): Show |
intron_variant | MODIFIER | c.-29+12004T>C | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 1/10 | chrX | 3053667 | |||||||
chrX:3053758 | A | AT | 12 | a0001c0001t0001g0020 a0001c0001t0001g0063 a0001c0001t0001g0091 others(9): Show |
12 | HG00099.hp1 HG00741.hp2 HG01106.hp1 others(9): Show |
intron_variant | MODIFIER | c.-29+12115dupT | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chrX | 3053758 | ||||||
chrX:3053758 | AT | A | 16 | a0001c0001t0001g0035 a0001c0001t0001g0036 a0001c0001t0001g0037 others(13): Show |
16 | HG01168.hp1 HG01169.hp2 HG01496.hp1 others(13): Show |
intron_variant | MODIFIER | c.-29+12115delT | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chrX | 3053758 | ||||||
chrX:3053760 | T | A | 1 | a0001c0012t0001g0089 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.-29+12097T>A | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 1/10 | chrX | 3053760 | |||||||
chrX:3053761 | T | A | 1 | a0001c0001t0001g0032 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.-29+12098T>A | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 1/10 | chrX | 3053761 | |||||||
chrX:3054063 | AC | A | 4 | a0001c0001t0001g0057 a0001c0001t0001g0058 a0001c0001t0001g0059 others(1): Show |
4 | HG01069.hp1 HG01071.hp1 HG01358.hp1 others(1): Show |
intron_variant | MODIFIER | c.-29+12402delC | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chrX | 3054063 | ||||||
chrX:3054546 | G | A | 2 | a0001c0001t0001g0032 a0001c0012t0001g0089 |
2 | NA19030.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.-29+12883G>A | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 1/10 | chrX | 3054546 | |||||||
chrX:3054574 | G | T | 1 | a0001c0001t0001g0154 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.-29+12911G>T | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 1/10 | chrX | 3054574 | |||||||
chrX:3054762 | T | G | 1 | a0001c0001t0001g0097 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.-29+13099T>G | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 1/10 | chrX | 3054762 | |||||||
chrX:3054796 | C | A | 6 | a0001c0002t0001g0181 a0001c0002t0001g0183 a0001c0002t0001g0184 others(3): Show |
6 | HG01109.hp1 HG02257.hp2 HG02622.hp2 others(3): Show |
intron_variant | MODIFIER | c.-29+13133C>A | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 1/10 | chrX | 3054796 | |||||||
chrX:3054803 | G | A | 2 | a0001c0001t0001g0032 a0001c0012t0001g0089 |
2 | NA19030.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.-29+13140G>A | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 1/10 | chrX | 3054803 | |||||||
chrX:3054942 | T | TA | 22 | a0001c0001t0001g0032 a0001c0001t0001g0035 a0001c0001t0001g0036 others(19): Show |
22 | HG01070.hp1 HG01071.hp2 HG01109.hp1 others(19): Show |
intron_variant | MODIFIER | c.-28-13131_-28-1313 others(5): Show |
ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 1/10 | chrX | 3054942 | |||||||
chrX:3055338 | A | G | 20 | a0001c0001t0001g0035 a0001c0001t0001g0036 a0001c0001t0001g0037 others(17): Show |
20 | HG01070.hp1 HG01071.hp2 HG01109.hp1 others(17): Show |
intron_variant | MODIFIER | c.-28-12735A>G | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 1/10 | chrX | 3055338 | |||||||
chrX:3055342 | C | CA | 19 | a0001c0001t0001g0032 a0001c0001t0001g0035 a0001c0001t0001g0047 others(16): Show |
19 | HG00597.hp2 HG00621.hp1 HG00673.hp1 others(16): Show |
intron_variant | MODIFIER | c.-28-12708dupA | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chrX | 3055342 | ||||||
chrX:3055342 | C | CAA | 7 | a0001c0001t0001g0166 a0001c0002t0001g0181 a0001c0002t0001g0183 others(4): Show |
7 | HG01109.hp1 HG02257.hp2 HG02622.hp2 others(4): Show |
intron_variant | MODIFIER | c.-28-12709_-28-1270 others(6): Show |
ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chrX | 3055342 | ||||||
chrX:3055342 | C | CAAAAAAA others(5): Show |
1 | a0001c0001t0001g0041 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.-28-12719_-28-1270 others(16): Show |
ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chrX | 3055342 | ||||||
chrX:3055342 | C | CAAAAAAA others(6): Show |
3 | a0001c0001t0001g0038 a0001c0001t0001g0039 a0002c0004t0001g0180 |
3 | HG01070.hp1 HG02451.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.-28-12720_-28-1270 others(17): Show |
ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chrX | 3055342 | ||||||
chrX:3055342 | C | CAAAAAAA others(7): Show |
4 | a0001c0001t0001g0036 a0001c0001t0001g0037 a0002c0004t0001g0090 others(1): Show |
4 | HG01071.hp2 HG02622.hp1 HG02895.hp1 others(1): Show |
intron_variant | MODIFIER | c.-28-12721_-28-1270 others(18): Show |
ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chrX | 3055342 | ||||||
chrX:3055342 | C | CAAAAAAA others(13): Show |
2 | a0004c0006t0001g0008 a0004c0006t0001g0009 |
2 | HG01168.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.-28-12727_-28-1270 others(24): Show |
ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chrX | 3055342 | ||||||
chrX:3055342 | CA | C | 10 | a0001c0001t0001g0019 a0001c0001t0001g0057 a0001c0001t0001g0058 others(7): Show |
10 | HG01069.hp1 HG01071.hp1 HG01167.hp1 others(7): Show |
intron_variant | MODIFIER | c.-28-12708delA | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chrX | 3055342 | ||||||
chrX:3055566 | T | C | 11 | a0001c0001t0001g0001 a0001c0001t0001g0047 a0001c0001t0001g0048 others(8): Show |
12 | HG00738.hp1 HG01256.hp1 HG01952.hp1 others(9): Show |
intron_variant | MODIFIER | c.-28-12507T>C | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 1/10 | chrX | 3055566 | |||||||
chrX:3055589 | C | G | 14 | a0001c0001t0001g0035 a0001c0001t0001g0036 a0001c0001t0001g0037 others(11): Show |
14 | HG01070.hp1 HG01071.hp2 HG01168.hp1 others(11): Show |
intron_variant | MODIFIER | c.-28-12484C>G | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 1/10 | chrX | 3055589 | |||||||
chrX:3055799 | T | A | 1 | a0001c0005t0001g0042 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.-28-12274T>A | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 1/10 | chrX | 3055799 | |||||||
chrX:3055877 | C | T | 3 | a0001c0001t0001g0061 a0001c0001t0001g0062 a0001c0001t0001g0063 |
3 | HG00323.hp2 HG01106.hp1 HG01496.hp1 |
intron_variant | MODIFIER | c.-28-12196C>T | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 1/10 | chrX | 3055877 | |||||||
chrX:3055961 | A | T | 6 | a0001c0002t0001g0181 a0001c0002t0001g0183 a0001c0002t0001g0184 others(3): Show |
6 | HG01109.hp1 HG02257.hp2 HG02622.hp2 others(3): Show |
intron_variant | MODIFIER | c.-28-12112A>T | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 1/10 | chrX | 3055961 | |||||||
chrX:3055969 | C | T | 14 | a0001c0001t0001g0035 a0001c0001t0001g0036 a0001c0001t0001g0037 others(11): Show |
14 | HG01070.hp1 HG01071.hp2 HG01168.hp1 others(11): Show |
intron_variant | MODIFIER | c.-28-12104C>T | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 1/10 | chrX | 3055969 | |||||||
chrX:3055994 | C | T | 1 | a0001c0001t0001g0019 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.-28-12079C>T | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 1/10 | chrX | 3055994 | |||||||
chrX:3055995 | G | A | 3 | a0002c0004t0001g0090 a0002c0004t0001g0179 a0002c0004t0001g0180 |
3 | HG01070.hp1 HG01071.hp2 HG02622.hp1 |
intron_variant | MODIFIER | c.-28-12078G>A | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 1/10 | chrX | 3055995 | |||||||
chrX:3056021 | G | A | 1 | a0001c0001t0001g0032 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.-28-12052G>A | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 1/10 | chrX | 3056021 | |||||||
chrX:3056040 | T | C | 6 | a0001c0002t0001g0181 a0001c0002t0001g0183 a0001c0002t0001g0184 others(3): Show |
6 | HG01109.hp1 HG02257.hp2 HG02622.hp2 others(3): Show |
intron_variant | MODIFIER | c.-28-12033T>C | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 1/10 | chrX | 3056040 | |||||||
chrX:3056181 | A | G | 12 | a0001c0001t0001g0035 a0001c0001t0001g0036 a0001c0001t0001g0037 others(9): Show |
12 | HG01070.hp1 HG01071.hp2 HG02280.hp1 others(9): Show |
intron_variant | MODIFIER | c.-28-11892A>G | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 1/10 | chrX | 3056181 | |||||||
chrX:3056253 | G | A | 6 | a0001c0002t0001g0181 a0001c0002t0001g0183 a0001c0002t0001g0184 others(3): Show |
6 | HG01109.hp1 HG02257.hp2 HG02622.hp2 others(3): Show |
intron_variant | MODIFIER | c.-28-11820G>A | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 1/10 | chrX | 3056253 | |||||||
chrX:3056275 | A | AT | 6 | a0001c0001t0001g0032 a0001c0001t0001g0056 a0001c0001t0001g0151 others(3): Show |
6 | HG00099.hp1 HG01258.hp1 NA19007.hp1 others(3): Show |
intron_variant | MODIFIER | c.-28-11780dupT | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chrX | 3056275 | ||||||
chrX:3056275 | AT | A | 6 | a0001c0001t0001g0036 a0001c0001t0001g0052 a0001c0001t0001g0092 others(3): Show |
6 | HG01167.hp1 HG01168.hp1 HG02895.hp1 others(3): Show |
intron_variant | MODIFIER | c.-28-11780delT | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chrX | 3056275 | ||||||
chrX:3056441 | A | G | 2 | a0004c0006t0001g0008 a0004c0006t0001g0009 |
2 | HG01168.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.-28-11632A>G | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 1/10 | chrX | 3056441 | |||||||
chrX:3056574 | C | T | 6 | a0001c0002t0001g0181 a0001c0002t0001g0183 a0001c0002t0001g0184 others(3): Show |
6 | HG01109.hp1 HG02257.hp2 HG02622.hp2 others(3): Show |
intron_variant | MODIFIER | c.-28-11499C>T | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 1/10 | chrX | 3056574 | |||||||
chrX:3056746 | A | G | 6 | a0001c0002t0001g0181 a0001c0002t0001g0183 a0001c0002t0001g0184 others(3): Show |
6 | HG01109.hp1 HG02257.hp2 HG02622.hp2 others(3): Show |
intron_variant | MODIFIER | c.-28-11327A>G | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 1/10 | chrX | 3056746 | |||||||
chrX:3056816 | T | C | 4 | a0001c0001t0001g0036 a0001c0001t0001g0037 a0001c0001t0001g0038 others(1): Show |
4 | HG02451.hp1 HG02895.hp1 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.-28-11257T>C | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 1/10 | chrX | 3056816 | |||||||
chrX:3056875 | A | T | 18 | a0001c0001t0001g0035 a0001c0001t0001g0036 a0001c0001t0001g0037 others(15): Show |
18 | HG01070.hp1 HG01071.hp2 HG01109.hp1 others(15): Show |
intron_variant | MODIFIER | c.-28-11198A>T | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 1/10 | chrX | 3056875 | |||||||
chrX:3057053 | C | T | 2 | a0001c0007t0003g0031 a0001c0007t0003g0182 |
2 | HG02257.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.-28-11020C>T | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 1/10 | chrX | 3057053 | |||||||
chrX:3057260 | C | T | 1 | a0001c0001t0001g0109 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.-28-10813C>T | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 1/10 | chrX | 3057260 | |||||||
chrX:3057364 | T | C | 20 | a0001c0001t0001g0035 a0001c0001t0001g0036 a0001c0001t0001g0037 others(17): Show |
20 | HG01070.hp1 HG01071.hp2 HG01109.hp1 others(17): Show |
intron_variant | MODIFIER | c.-28-10709T>C | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 1/10 | chrX | 3057364 | |||||||
chrX:3057384 | A | G | 2 | a0001c0007t0003g0031 a0001c0007t0003g0182 |
2 | HG02257.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.-28-10689A>G | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 1/10 | chrX | 3057384 | |||||||
chrX:3057459 | A | G | 18 | a0001c0001t0001g0035 a0001c0001t0001g0036 a0001c0001t0001g0037 others(15): Show |
18 | HG01070.hp1 HG01071.hp2 HG01109.hp1 others(15): Show |
intron_variant | MODIFIER | c.-28-10614A>G | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 1/10 | chrX | 3057459 | |||||||
chrX:3057489 | G | A | 2 | a0001c0001t0001g0032 a0001c0012t0001g0089 |
2 | NA19030.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.-28-10584G>A | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 1/10 | chrX | 3057489 | |||||||
chrX:3057516 | G | A | 2 | a0001c0007t0003g0031 a0001c0007t0003g0182 |
2 | HG02257.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.-28-10557G>A | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 1/10 | chrX | 3057516 | |||||||
chrX:3057916 | G | A | 17 | a0001c0001t0001g0035 a0001c0001t0001g0036 a0001c0001t0001g0037 others(14): Show |
17 | HG01070.hp1 HG01071.hp2 HG01109.hp1 others(14): Show |
intron_variant | MODIFIER | c.-28-10157G>A | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 1/10 | chrX | 3057916 | |||||||
chrX:3057946 | G | A | 1 | a0001c0002t0001g0184 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.-28-10127G>A | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 1/10 | chrX | 3057946 | |||||||
chrX:3058065 | C | T | 19 | a0001c0001t0001g0035 a0001c0001t0001g0036 a0001c0001t0001g0037 others(16): Show |
19 | HG01070.hp1 HG01071.hp2 HG01109.hp1 others(16): Show |
intron_variant | MODIFIER | c.-28-10008C>T | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 1/10 | chrX | 3058065 | |||||||
chrX:3058289 | T | TG | 2 | a0001c0007t0003g0031 a0001c0007t0003g0182 |
2 | HG02257.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.-28-9784_-28-9783i others(3): Show |
ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 1/10 | chrX | 3058289 | |||||||
chrX:3058298 | G | A | 2 | a0001c0007t0003g0031 a0001c0007t0003g0182 |
2 | HG02257.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.-28-9775G>A | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 1/10 | chrX | 3058298 | |||||||
chrX:3058339 | C | G | 1 | a0001c0001t0001g0052 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.-28-9734C>G | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 1/10 | chrX | 3058339 | |||||||
chrX:3058426 | C | T | 2 | a0001c0007t0003g0031 a0001c0007t0003g0182 |
2 | HG02257.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.-28-9647C>T | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 1/10 | chrX | 3058426 | |||||||
chrX:3058453 | G | C | 2 | a0001c0007t0003g0031 a0001c0007t0003g0182 |
2 | HG02257.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.-28-9620G>C | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 1/10 | chrX | 3058453 | |||||||
chrX:3058645 | G | A | 17 | a0001c0001t0001g0035 a0001c0001t0001g0036 a0001c0001t0001g0037 others(14): Show |
17 | HG01070.hp1 HG01071.hp2 HG01109.hp1 others(14): Show |
intron_variant | MODIFIER | c.-28-9428G>A | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 1/10 | chrX | 3058645 | |||||||
chrX:3058673 | G | A | 4 | a0001c0001t0001g0110 a0001c0001t0001g0111 a0001c0001t0001g0112 others(1): Show |
4 | NA18957.hp1 NA18988.hp1 NA19004.hp1 others(1): Show |
intron_variant | MODIFIER | c.-28-9400G>A | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 1/10 | chrX | 3058673 | |||||||
chrX:3058674 | G | A | 17 | a0001c0001t0001g0035 a0001c0001t0001g0036 a0001c0001t0001g0037 others(14): Show |
17 | HG01070.hp1 HG01071.hp2 HG01109.hp1 others(14): Show |
intron_variant | MODIFIER | c.-28-9399G>A | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 1/10 | chrX | 3058674 | |||||||
chrX:3058759 | G | T | 2 | a0001c0007t0003g0031 a0001c0007t0003g0182 |
2 | HG02257.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.-28-9314G>T | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 1/10 | chrX | 3058759 | |||||||
chrX:3058832 | A | G | 19 | a0001c0001t0001g0035 a0001c0001t0001g0036 a0001c0001t0001g0037 others(16): Show |
19 | HG01070.hp1 HG01071.hp2 HG01109.hp1 others(16): Show |
intron_variant | MODIFIER | c.-28-9241A>G | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 1/10 | chrX | 3058832 | |||||||
chrX:3058929 | T | C | 2 | a0001c0007t0003g0031 a0001c0007t0003g0182 |
2 | HG02257.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.-28-9144T>C | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 1/10 | chrX | 3058929 | |||||||
chrX:3059190 | C | T | 5 | a0001c0001t0001g0149 a0001c0001t0001g0150 a0001c0001t0001g0170 others(2): Show |
5 | HG01515.hp1 HG01517.hp2 HG02257.hp2 others(2): Show |
intron_variant | MODIFIER | c.-28-8883C>T | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 1/10 | chrX | 3059190 | |||||||
chrX:3059353 | C | T | 2 | a0001c0001t0001g0032 a0001c0012t0001g0089 |
2 | NA19030.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.-28-8720C>T | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 1/10 | chrX | 3059353 | |||||||
chrX:3059388 | C | T | 1 | a0001c0001t0001g0148 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.-28-8685C>T | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 1/10 | chrX | 3059388 | |||||||
chrX:3059527 | T | A | 2 | a0001c0007t0003g0031 a0001c0007t0003g0182 |
2 | HG02257.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.-28-8546T>A | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 1/10 | chrX | 3059527 | |||||||
chrX:3059553 | T | A | 2 | a0004c0006t0001g0008 a0004c0006t0001g0009 |
2 | HG01168.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.-28-8520T>A | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 1/10 | chrX | 3059553 | |||||||
chrX:3059643 | C | A | 3 | a0002c0004t0001g0090 a0002c0004t0001g0179 a0002c0004t0001g0180 |
3 | HG01070.hp1 HG01071.hp2 HG02622.hp1 |
intron_variant | MODIFIER | c.-28-8430C>A | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 1/10 | chrX | 3059643 | |||||||
chrX:3059647 | C | T | 2 | a0001c0007t0003g0031 a0001c0007t0003g0182 |
2 | HG02257.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.-28-8426C>T | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 1/10 | chrX | 3059647 | |||||||
chrX:3059649 | C | G | 4 | a0001c0001t0001g0054 a0001c0001t0001g0103 a0001c0001t0001g0147 others(1): Show |
4 | HG00673.hp1 HG02027.hp1 NA18747.hp1 others(1): Show |
intron_variant | MODIFIER | c.-28-8424C>G | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 1/10 | chrX | 3059649 | |||||||
chrX:3059729 | G | T | 2 | a0001c0007t0003g0031 a0001c0007t0003g0182 |
2 | HG02257.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.-28-8344G>T | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 1/10 | chrX | 3059729 | |||||||
chrX:3059971 | G | A | 1 | a0001c0001t0001g0163 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.-28-8102G>A | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 1/10 | chrX | 3059971 | |||||||
chrX:3059995 | C | T | 1 | a0001c0001t0001g0109 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.-28-8078C>T | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 1/10 | chrX | 3059995 | |||||||
chrX:3060027 | C | T | 1 | a0001c0001t0001g0146 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.-28-8046C>T | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 1/10 | chrX | 3060027 | |||||||
chrX:3060220 | T | C | 21 | a0001c0001t0001g0032 a0001c0001t0001g0035 a0001c0001t0001g0036 others(18): Show |
21 | HG01070.hp1 HG01071.hp2 HG01109.hp1 others(18): Show |
intron_variant | MODIFIER | c.-28-7853T>C | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 1/10 | chrX | 3060220 | |||||||
chrX:3060253 | A | G | 1 | a0001c0015t0006g0021 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.-28-7820A>G | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 1/10 | chrX | 3060253 | |||||||
chrX:3060373 | G | C | 2 | a0001c0001t0001g0007 a0001c0001t0001g0175 |
3 | NA18951.hp1 NA18994.hp1 NA19089.hp1 |
intron_variant | MODIFIER | c.-28-7700G>C | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 1/10 | chrX | 3060373 | |||||||
chrX:3060396 | T | G | 2 | a0001c0007t0003g0031 a0001c0007t0003g0182 |
2 | HG02257.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.-28-7677T>G | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 1/10 | chrX | 3060396 | |||||||
chrX:3060430 | C | T | 17 | a0001c0001t0001g0035 a0001c0001t0001g0036 a0001c0001t0001g0037 others(14): Show |
17 | HG01070.hp1 HG01071.hp2 HG01109.hp1 others(14): Show |
intron_variant | MODIFIER | c.-28-7643C>T | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 1/10 | chrX | 3060430 | |||||||
chrX:3060442 | G | C | 19 | a0001c0001t0001g0035 a0001c0001t0001g0036 a0001c0001t0001g0037 others(16): Show |
19 | HG01070.hp1 HG01071.hp2 HG01109.hp1 others(16): Show |
intron_variant | MODIFIER | c.-28-7631G>C | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 1/10 | chrX | 3060442 | |||||||
chrX:3060529 | A | G | 2 | a0001c0007t0003g0031 a0001c0007t0003g0182 |
2 | HG02257.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.-28-7544A>G | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 1/10 | chrX | 3060529 | |||||||
chrX:3060641 | C | T | 1 | a0001c0001t0001g0053 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.-28-7432C>T | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 1/10 | chrX | 3060641 | |||||||
chrX:3060895 | A | G | 2 | a0001c0007t0003g0031 a0001c0007t0003g0182 |
2 | HG02257.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.-28-7178A>G | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 1/10 | chrX | 3060895 | |||||||
chrX:3060957 | T | C | 1 | a0001c0001t0001g0114 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.-28-7116T>C | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 1/10 | chrX | 3060957 | |||||||
chrX:3061028 | A | C | 1 | a0001c0001t0001g0056 | 1 | NA19072.hp1 | intron_variant | MODIFIER | c.-28-7045A>C | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 1/10 | chrX | 3061028 | |||||||
chrX:3061198 | T | A | 2 | a0001c0007t0003g0031 a0001c0007t0003g0182 |
2 | HG02257.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.-28-6875T>A | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 1/10 | chrX | 3061198 | |||||||
chrX:3061601 | G | A | 2 | a0001c0001t0001g0032 a0001c0012t0001g0089 |
2 | NA19030.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.-28-6472G>A | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 1/10 | chrX | 3061601 | |||||||
chrX:3061602 | G | A | 2 | a0001c0007t0003g0031 a0001c0007t0003g0182 |
2 | HG02257.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.-28-6471G>A | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 1/10 | chrX | 3061602 | |||||||
chrX:3061628 | A | C | 146 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(143): Show |
153 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(150): Show |
intron_variant | MODIFIER | c.-28-6445A>C | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 1/10 | chrX | 3061628 | |||||||
chrX:3061685 | G | A | 1 | a0001c0002t0001g0015 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.-28-6388G>A | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 1/10 | chrX | 3061685 | |||||||
chrX:3061872 | T | A | 1 | a0001c0015t0006g0021 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.-28-6201T>A | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 1/10 | chrX | 3061872 | |||||||
chrX:3061893 | C | T | 4 | a0001c0001t0001g0035 a0001c0010t0001g0033 a0001c0010t0001g0040 others(1): Show |
4 | HG02280.hp1 HG02809.hp1 NA20129.hp1 others(1): Show |
intron_variant | MODIFIER | c.-28-6180C>T | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 1/10 | chrX | 3061893 | |||||||
chrX:3061937 | C | T | 1 | a0001c0007t0003g0182 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.-28-6136C>T | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 1/10 | chrX | 3061937 | |||||||
chrX:3062168 | A | G | 17 | a0001c0001t0001g0035 a0001c0001t0001g0036 a0001c0001t0001g0037 others(14): Show |
17 | HG01070.hp1 HG01071.hp2 HG01109.hp1 others(14): Show |
intron_variant | MODIFIER | c.-28-5905A>G | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 1/10 | chrX | 3062168 | |||||||
chrX:3062300 | A | G | 2 | a0001c0007t0003g0031 a0001c0007t0003g0182 |
2 | HG02257.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.-28-5773A>G | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 1/10 | chrX | 3062300 | |||||||
chrX:3062355 | T | G | 2 | a0001c0007t0003g0031 a0001c0007t0003g0182 |
2 | HG02257.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.-28-5718T>G | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 1/10 | chrX | 3062355 | |||||||
chrX:3062516 | T | C | 2 | a0001c0007t0003g0031 a0001c0007t0003g0182 |
2 | HG02257.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.-28-5557T>C | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 1/10 | chrX | 3062516 | |||||||
chrX:3062551 | C | T | 4 | a0001c0001t0001g0036 a0001c0001t0001g0037 a0001c0001t0001g0038 others(1): Show |
4 | HG02451.hp1 HG02895.hp1 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.-28-5522C>T | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 1/10 | chrX | 3062551 | |||||||
chrX:3062620 | A | T | 2 | a0001c0007t0003g0031 a0001c0007t0003g0182 |
2 | HG02257.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.-28-5453A>T | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 1/10 | chrX | 3062620 | |||||||
chrX:3062659 | G | A | 2 | a0001c0007t0003g0031 a0001c0007t0003g0182 |
2 | HG02257.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.-28-5414G>A | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 1/10 | chrX | 3062659 | |||||||
chrX:3062686 | A | G | 1 | a0001c0001t0001g0178 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.-28-5387A>G | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 1/10 | chrX | 3062686 | |||||||
chrX:3062716 | A | C | 1 | a0001c0001t0001g0145 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.-28-5357A>C | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 1/10 | chrX | 3062716 | |||||||
chrX:3062720 | T | C | 20 | a0001c0001t0001g0032 a0001c0001t0001g0035 a0001c0001t0001g0036 others(17): Show |
20 | HG01070.hp1 HG01071.hp2 HG01109.hp1 others(17): Show |
intron_variant | MODIFIER | c.-28-5353T>C | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 1/10 | chrX | 3062720 | |||||||
chrX:3062722 | T | C | 2 | a0001c0007t0003g0031 a0001c0007t0003g0182 |
2 | HG02257.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.-28-5351T>C | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 1/10 | chrX | 3062722 | |||||||
chrX:3062971 | T | C | 2 | a0001c0007t0003g0031 a0001c0007t0003g0182 |
2 | HG02257.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.-28-5102T>C | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 1/10 | chrX | 3062971 | |||||||
chrX:3063122 | C | T | 1 | a0001c0012t0001g0089 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.-28-4951C>T | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 1/10 | chrX | 3063122 | |||||||
chrX:3063434 | A | G | 1 | a0002c0003t0001g0144 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.-28-4639A>G | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 1/10 | chrX | 3063434 | |||||||
chrX:3063435 | G | C | 2 | a0001c0007t0003g0031 a0001c0007t0003g0182 |
2 | HG02257.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.-28-4638G>C | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 1/10 | chrX | 3063435 | |||||||
chrX:3063463 | G | A | 17 | a0001c0001t0001g0035 a0001c0001t0001g0036 a0001c0001t0001g0037 others(14): Show |
17 | HG01070.hp1 HG01071.hp2 HG01109.hp1 others(14): Show |
intron_variant | MODIFIER | c.-28-4610G>A | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 1/10 | chrX | 3063463 | |||||||
chrX:3063486 | T | A | 2 | a0001c0007t0003g0031 a0001c0007t0003g0182 |
2 | HG02257.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.-28-4587T>A | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 1/10 | chrX | 3063486 | |||||||
chrX:3063794 | C | G | 2 | a0001c0007t0003g0031 a0001c0007t0003g0182 |
2 | HG02257.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.-28-4279C>G | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 1/10 | chrX | 3063794 | |||||||
chrX:3064360 | C | T | 2 | a0001c0007t0003g0031 a0001c0007t0003g0182 |
2 | HG02257.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.-28-3713C>T | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 1/10 | chrX | 3064360 | |||||||
chrX:3064427 | G | T | 1 | a0001c0002t0001g0024 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.-28-3646G>T | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 1/10 | chrX | 3064427 | |||||||
chrX:3064470 | A | C | 2 | a0001c0007t0003g0031 a0001c0007t0003g0182 |
2 | HG02257.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.-28-3603A>C | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 1/10 | chrX | 3064470 | |||||||
chrX:3064583 | A | G | 1 | a0001c0001t0001g0078 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.-28-3490A>G | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 1/10 | chrX | 3064583 | |||||||
chrX:3064748 | C | A | 2 | a0001c0007t0003g0031 a0001c0007t0003g0182 |
2 | HG02257.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.-28-3325C>A | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 1/10 | chrX | 3064748 | |||||||
chrX:3064854 | G | A | 2 | a0001c0001t0001g0082 a0001c0001t0001g0083 |
2 | NA18952.hp1 NA18990.hp1 |
intron_variant | MODIFIER | c.-28-3219G>A | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 1/10 | chrX | 3064854 | |||||||
chrX:3064957 | A | G | 2 | a0001c0007t0003g0031 a0001c0007t0003g0182 |
2 | HG02257.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.-28-3116A>G | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 1/10 | chrX | 3064957 | |||||||
chrX:3065211 | C | A | 1 | a0001c0002t0001g0067 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.-28-2862C>A | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 1/10 | chrX | 3065211 | |||||||
chrX:3065297 | T | G | 21 | a0001c0001t0001g0032 a0001c0001t0001g0035 a0001c0001t0001g0036 others(18): Show |
21 | HG01070.hp1 HG01071.hp2 HG01109.hp1 others(18): Show |
intron_variant | MODIFIER | c.-28-2776T>G | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 1/10 | chrX | 3065297 | |||||||
chrX:3065313 | T | C | 2 | a0001c0001t0001g0109 a0003c0008t0001g0115 |
2 | HG02258.hp1 NA18946.hp1 |
intron_variant | MODIFIER | c.-28-2760T>C | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 1/10 | chrX | 3065313 | |||||||
chrX:3065321 | G | A | 2 | a0001c0007t0003g0031 a0001c0007t0003g0182 |
2 | HG02257.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.-28-2752G>A | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 1/10 | chrX | 3065321 | |||||||
chrX:3065353 | C | T | 2 | a0001c0007t0003g0031 a0001c0007t0003g0182 |
2 | HG02257.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.-28-2720C>T | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 1/10 | chrX | 3065353 | |||||||
chrX:3065435 | AAAAT | A | 3 | a0001c0007t0003g0031 a0001c0007t0003g0182 a0001c0012t0001g0089 |
3 | HG02257.hp2 HG02965.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.-28-2610_-28-2607d others(6): Show |
ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chrX | 3065435 | ||||||
chrX:3065459 | T | G | 1 | a0005c0011t0001g0034 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.-28-2614T>G | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 1/10 | chrX | 3065459 | |||||||
chrX:3065636 | C | CA | 11 | a0001c0001t0001g0036 a0001c0001t0001g0037 a0001c0001t0001g0038 others(8): Show |
11 | HG00323.hp2 HG01168.hp1 HG01169.hp2 others(8): Show |
intron_variant | MODIFIER | c.-28-2422dupA | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chrX | 3065636 | ||||||
chrX:3065636 | C | CAA | 11 | a0001c0001t0001g0035 a0001c0002t0001g0181 a0001c0002t0001g0183 others(8): Show |
11 | HG01070.hp1 HG01071.hp2 HG01109.hp1 others(8): Show |
intron_variant | MODIFIER | c.-28-2423_-28-2422d others(4): Show |
ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chrX | 3065636 | ||||||
chrX:3065636 | C | CCA | 3 | a0001c0007t0003g0031 a0001c0007t0003g0182 a0001c0012t0001g0089 |
3 | HG02257.hp2 HG02965.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.-28-2437_-28-2436i others(4): Show |
ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 1/10 | chrX | 3065636 | |||||||
chrX:3065797 | A | G | 21 | a0001c0001t0001g0032 a0001c0001t0001g0035 a0001c0001t0001g0036 others(18): Show |
21 | HG01070.hp1 HG01071.hp2 HG01109.hp1 others(18): Show |
intron_variant | MODIFIER | c.-28-2276A>G | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 1/10 | chrX | 3065797 | |||||||
chrX:3065825 | G | A | 20 | a0001c0001t0001g0032 a0001c0001t0001g0035 a0001c0001t0001g0036 others(17): Show |
20 | HG01070.hp1 HG01071.hp2 HG01109.hp1 others(17): Show |
intron_variant | MODIFIER | c.-28-2248G>A | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 1/10 | chrX | 3065825 | |||||||
chrX:3065857 | G | A | 1 | a0001c0001t0001g0032 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.-28-2216G>A | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 1/10 | chrX | 3065857 | |||||||
chrX:3065913 | A | G | 20 | a0001c0001t0001g0032 a0001c0001t0001g0035 a0001c0001t0001g0036 others(17): Show |
20 | HG01070.hp1 HG01071.hp2 HG01109.hp1 others(17): Show |
intron_variant | MODIFIER | c.-28-2160A>G | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 1/10 | chrX | 3065913 | |||||||
chrX:3066232 | A | T | 1 | a0001c0012t0001g0089 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.-28-1841A>T | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 1/10 | chrX | 3066232 | |||||||
chrX:3066308 | C | T | 2 | a0001c0007t0003g0031 a0001c0007t0003g0182 |
2 | HG02257.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.-28-1765C>T | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 1/10 | chrX | 3066308 | |||||||
chrX:3066426 | T | A | 1 | a0001c0012t0001g0089 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.-28-1647T>A | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 1/10 | chrX | 3066426 | |||||||
chrX:3066538 | G | A | 1 | a0001c0001t0001g0056 | 1 | NA19072.hp1 | intron_variant | MODIFIER | c.-28-1535G>A | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 1/10 | chrX | 3066538 | |||||||
chrX:3066626 | T | C | 4 | a0001c0001t0001g0036 a0001c0001t0001g0037 a0001c0001t0001g0038 others(1): Show |
4 | HG02451.hp1 HG02895.hp1 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.-28-1447T>C | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 1/10 | chrX | 3066626 | |||||||
chrX:3066845 | G | C | 1 | a0001c0012t0001g0089 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.-28-1228G>C | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 1/10 | chrX | 3066845 | |||||||
chrX:3066912 | C | CT | 15 | a0001c0001t0001g0035 a0001c0001t0001g0036 a0001c0001t0001g0038 others(12): Show |
15 | HG01070.hp1 HG01071.hp2 HG01109.hp1 others(12): Show |
intron_variant | MODIFIER | c.-28-1145dupT | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chrX | 3066912 | ||||||
chrX:3066912 | CT | C | 142 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(139): Show |
149 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(146): Show |
intron_variant | MODIFIER | c.-28-1145delT | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chrX | 3066912 | ||||||
chrX:3066912 | CTT | C | 7 | a0001c0001t0001g0056 a0001c0001t0001g0062 a0001c0001t0001g0078 others(4): Show |
7 | HG00323.hp2 HG03017.hp1 HG03942.hp1 others(4): Show |
intron_variant | MODIFIER | c.-28-1146_-28-1145d others(4): Show |
ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chrX | 3066912 | ||||||
chrX:3066945 | G | A | 3 | a0001c0001t0001g0032 a0001c0007t0003g0031 a0001c0007t0003g0182 |
3 | HG02257.hp2 HG02965.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.-28-1128G>A | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 1/10 | chrX | 3066945 | |||||||
chrX:3066981 | T | C | 3 | a0001c0001t0001g0032 a0001c0007t0003g0031 a0001c0007t0003g0182 |
3 | HG02257.hp2 HG02965.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.-28-1092T>C | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 1/10 | chrX | 3066981 | |||||||
chrX:3067067 | C | T | 1 | a0001c0001t0001g0045 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.-28-1006C>T | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 1/10 | chrX | 3067067 | |||||||
chrX:3067104 | C | T | 18 | a0001c0001t0001g0035 a0001c0001t0001g0036 a0001c0001t0001g0037 others(15): Show |
18 | HG01070.hp1 HG01071.hp2 HG01109.hp1 others(15): Show |
intron_variant | MODIFIER | c.-28-969C>T | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 1/10 | chrX | 3067104 | |||||||
chrX:3067131 | C | CGT | 2 | a0001c0005t0001g0010 a0001c0005t0001g0012 |
2 | HG03041.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.-28-924_-28-923dup others(2): Show |
ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chrX | 3067131 | ||||||
chrX:3067131 | CGTGT | C | 21 | a0001c0001t0001g0032 a0001c0001t0001g0035 a0001c0001t0001g0036 others(18): Show |
21 | HG01070.hp1 HG01071.hp2 HG01109.hp1 others(18): Show |
intron_variant | MODIFIER | c.-28-926_-28-923del others(4): Show |
ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chrX | 3067131 | ||||||
chrX:3067193 | T | A | 18 | a0001c0001t0001g0035 a0001c0001t0001g0036 a0001c0001t0001g0037 others(15): Show |
18 | HG01070.hp1 HG01071.hp2 HG01109.hp1 others(15): Show |
intron_variant | MODIFIER | c.-28-880T>A | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 1/10 | chrX | 3067193 | |||||||
chrX:3067201 | A | T | 1 | a0001c0001t0001g0161 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.-28-872A>T | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 1/10 | chrX | 3067201 | |||||||
chrX:3067202 | T | C | 1 | a0001c0001t0001g0161 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.-28-871T>C | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 1/10 | chrX | 3067202 | |||||||
chrX:3067203 | A | C | 22 | a0001c0001t0001g0032 a0001c0001t0001g0035 a0001c0001t0001g0036 others(19): Show |
22 | HG01070.hp1 HG01071.hp2 HG01109.hp1 others(19): Show |
intron_variant | MODIFIER | c.-28-870A>C | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 1/10 | chrX | 3067203 | |||||||
chrX:3067280 | T | G | 1 | a0001c0001t0001g0118 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.-28-793T>G | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 1/10 | chrX | 3067280 | |||||||
chrX:3067387 | A | G | 1 | a0002c0003t0001g0050 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.-28-686A>G | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 1/10 | chrX | 3067387 | |||||||
chrX:3067416 | C | T | 145 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(142): Show |
152 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(149): Show |
intron_variant | MODIFIER | c.-28-657C>T | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 1/10 | chrX | 3067416 | |||||||
chrX:3067631 | G | A | 15 | a0001c0001t0001g0035 a0001c0001t0001g0036 a0001c0001t0001g0037 others(12): Show |
15 | HG01070.hp1 HG01071.hp2 HG01109.hp1 others(12): Show |
intron_variant | MODIFIER | c.-28-442G>A | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 1/10 | chrX | 3067631 | |||||||
chrX:3067731 | C | T | 1 | a0001c0001t0001g0143 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.-28-342C>T | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 1/10 | chrX | 3067731 | |||||||
chrX:3067840 | C | T | 1 | a0001c0001t0001g0142 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.-28-233C>T | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 1/10 | chrX | 3067840 | |||||||
chrX:3067852 | G | A | 1 | a0001c0012t0001g0089 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.-28-221G>A | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 1/10 | chrX | 3067852 | |||||||
chrX:3067856 | C | CA | 29 | a0001c0001t0001g0001 a0001c0001t0001g0035 a0001c0001t0001g0036 others(26): Show |
30 | HG00738.hp1 HG01070.hp1 HG01071.hp2 others(27): Show |
intron_variant | MODIFIER | c.-28-203dupA | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chrX | 3067856 | ||||||
chrX:3068020 | C | CT | 6 | a0001c0001t0001g0006 a0001c0001t0001g0032 a0001c0001t0001g0081 others(3): Show |
7 | HG02257.hp2 HG02486.hp1 HG02965.hp1 others(4): Show |
intron_variant | MODIFIER | c.-28-36dupT | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chrX | 3068020 | ||||||
chrX:3068020 | CT | C | 8 | a0001c0001t0001g0068 a0001c0001t0001g0069 a0001c0001t0001g0070 others(5): Show |
8 | HG02056.hp1 HG02572.hp1 HG02698.hp1 others(5): Show |
intron_variant | MODIFIER | c.-28-36delT | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chrX | 3068020 | ||||||
chrX:3068020 | CTT | C | 17 | a0001c0001t0001g0035 a0001c0001t0001g0036 a0001c0001t0001g0037 others(14): Show |
17 | HG01070.hp1 HG01071.hp2 HG01109.hp1 others(14): Show |
intron_variant | MODIFIER | c.-28-37_-28-36delTT | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chrX | 3068020 | ||||||
chrX:3068070 | A | G | 15 | a0001c0001t0001g0035 a0001c0001t0001g0036 a0001c0001t0001g0037 others(12): Show |
15 | HG01070.hp1 HG01071.hp2 HG01109.hp1 others(12): Show |
splice_region_variant&intron_variant | LOW | c.-28-3A>G | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 1/10 | chrX | 3068070 | |||||||
chrX:3068185 | C | T | 1 | a0001c0001t0001g0141 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.11+74C>T | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 2/10 | chrX | 3068185 | |||||||
chrX:3068221 | T | A | 19 | a0001c0001t0001g0032 a0001c0001t0001g0035 a0001c0001t0001g0036 others(16): Show |
19 | HG01070.hp1 HG01071.hp2 HG01109.hp1 others(16): Show |
intron_variant | MODIFIER | c.11+110T>A | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 2/10 | chrX | 3068221 | |||||||
chrX:3068572 | G | A | 4 | a0001c0001t0001g0032 a0001c0007t0003g0031 a0001c0007t0003g0182 others(1): Show |
4 | HG02257.hp2 HG02965.hp1 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.11+461G>A | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 2/10 | chrX | 3068572 | |||||||
chrX:3068762 | G | A | 7 | a0001c0001t0001g0032 a0001c0007t0003g0031 a0001c0007t0003g0182 others(4): Show |
7 | HG01168.hp1 HG01169.hp2 HG02257.hp2 others(4): Show |
intron_variant | MODIFIER | c.11+651G>A | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 2/10 | chrX | 3068762 | |||||||
chrX:3068765 | G | GATA | 7 | a0001c0001t0001g0032 a0001c0007t0003g0031 a0001c0007t0003g0182 others(4): Show |
7 | HG01168.hp1 HG01169.hp2 HG02257.hp2 others(4): Show |
intron_variant | MODIFIER | c.11+655_11+656insTA others(1): Show |
ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chrX | 3068765 | ||||||
chrX:3068806 | A | G | 7 | a0001c0001t0001g0032 a0001c0007t0003g0031 a0001c0007t0003g0182 others(4): Show |
7 | HG01168.hp1 HG01169.hp2 HG02257.hp2 others(4): Show |
intron_variant | MODIFIER | c.11+695A>G | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 2/10 | chrX | 3068806 | |||||||
chrX:3068888 | A | G | 7 | a0001c0001t0001g0032 a0001c0007t0003g0031 a0001c0007t0003g0182 others(4): Show |
7 | HG01168.hp1 HG01169.hp2 HG02257.hp2 others(4): Show |
intron_variant | MODIFIER | c.11+777A>G | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 2/10 | chrX | 3068888 | |||||||
chrX:3068907 | C | A | 7 | a0001c0001t0001g0032 a0001c0007t0003g0031 a0001c0007t0003g0182 others(4): Show |
7 | HG01168.hp1 HG01169.hp2 HG02257.hp2 others(4): Show |
intron_variant | MODIFIER | c.11+796C>A | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 2/10 | chrX | 3068907 | |||||||
chrX:3069033 | C | G | 7 | a0001c0001t0001g0032 a0001c0007t0003g0031 a0001c0007t0003g0182 others(4): Show |
7 | HG01168.hp1 HG01169.hp2 HG02257.hp2 others(4): Show |
intron_variant | MODIFIER | c.11+922C>G | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 2/10 | chrX | 3069033 | |||||||
chrX:3069169 | A | G | 1 | a0001c0012t0001g0089 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.11+1058A>G | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 2/10 | chrX | 3069169 | |||||||
chrX:3069321 | C | T | 4 | a0001c0001t0001g0032 a0001c0007t0003g0031 a0001c0007t0003g0182 others(1): Show |
4 | HG02257.hp2 HG02965.hp1 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.11+1210C>T | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 2/10 | chrX | 3069321 | |||||||
chrX:3069332 | C | CT | 7 | a0001c0001t0001g0032 a0001c0007t0003g0031 a0001c0007t0003g0182 others(4): Show |
7 | HG01168.hp1 HG01169.hp2 HG02257.hp2 others(4): Show |
intron_variant | MODIFIER | c.11+1226dupT | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chrX | 3069332 | ||||||
chrX:3069338 | C | T | 7 | a0001c0001t0001g0032 a0001c0007t0003g0031 a0001c0007t0003g0182 others(4): Show |
7 | HG01168.hp1 HG01169.hp2 HG02257.hp2 others(4): Show |
intron_variant | MODIFIER | c.11+1227C>T | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 2/10 | chrX | 3069338 | |||||||
chrX:3069359 | T | C | 1 | a0001c0016t0001g0155 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.11+1248T>C | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 2/10 | chrX | 3069359 | |||||||
chrX:3069385 | G | A | 4 | a0001c0001t0001g0032 a0001c0007t0003g0031 a0001c0007t0003g0182 others(1): Show |
4 | HG02257.hp2 HG02965.hp1 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.11+1274G>A | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 2/10 | chrX | 3069385 | |||||||
chrX:3069498 | A | AT | 7 | a0001c0001t0001g0032 a0001c0007t0003g0031 a0001c0007t0003g0182 others(4): Show |
7 | HG01168.hp1 HG01169.hp2 HG02257.hp2 others(4): Show |
intron_variant | MODIFIER | c.11+1394dupT | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chrX | 3069498 | ||||||
chrX:3069568 | C | T | 7 | a0001c0001t0001g0032 a0001c0007t0003g0031 a0001c0007t0003g0182 others(4): Show |
7 | HG01168.hp1 HG01169.hp2 HG02257.hp2 others(4): Show |
intron_variant | MODIFIER | c.11+1457C>T | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 2/10 | chrX | 3069568 | |||||||
chrX:3069697 | C | CT | 7 | a0001c0001t0001g0032 a0001c0007t0003g0031 a0001c0007t0003g0182 others(4): Show |
7 | HG01168.hp1 HG01169.hp2 HG02257.hp2 others(4): Show |
intron_variant | MODIFIER | c.11+1591dupT | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chrX | 3069697 | ||||||
chrX:3069720 | T | TA | 7 | a0001c0001t0001g0032 a0001c0007t0003g0031 a0001c0007t0003g0182 others(4): Show |
7 | HG01168.hp1 HG01169.hp2 HG02257.hp2 others(4): Show |
intron_variant | MODIFIER | c.11+1610dupA | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chrX | 3069720 | ||||||
chrX:3069721 | A | AT | 15 | a0001c0001t0001g0035 a0001c0001t0001g0036 a0001c0001t0001g0037 others(12): Show |
15 | HG01070.hp1 HG01071.hp2 HG01109.hp1 others(12): Show |
intron_variant | MODIFIER | c.11+1617dupT | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chrX | 3069721 | ||||||
chrX:3069722 | T | C | 1 | a0001c0001t0001g0177 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.11+1611T>C | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 2/10 | chrX | 3069722 | |||||||
chrX:3069875 | C | T | 1 | a0001c0001t0001g0047 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.11+1764C>T | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 2/10 | chrX | 3069875 | |||||||
chrX:3070240 | C | T | 1 | a0005c0022t0001g0169 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.12-1786C>T | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 2/10 | chrX | 3070240 | |||||||
chrX:3070315 | A | G | 15 | a0001c0001t0001g0035 a0001c0001t0001g0036 a0001c0001t0001g0037 others(12): Show |
15 | HG01070.hp1 HG01071.hp2 HG01109.hp1 others(12): Show |
intron_variant | MODIFIER | c.12-1711A>G | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 2/10 | chrX | 3070315 | |||||||
chrX:3070368 | T | C | 167 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(164): Show |
174 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(171): Show |
intron_variant | MODIFIER | c.12-1658T>C | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 2/10 | chrX | 3070368 | |||||||
chrX:3070590 | A | T | 176 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(173): Show |
183 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(180): Show |
intron_variant | MODIFIER | c.12-1436A>T | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 2/10 | chrX | 3070590 | |||||||
chrX:3070686 | T | C | 1 | a0002c0003t0001g0050 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.12-1340T>C | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 2/10 | chrX | 3070686 | |||||||
chrX:3070768 | T | C | 1 | a0001c0001t0001g0119 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.12-1258T>C | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 2/10 | chrX | 3070768 | |||||||
chrX:3070775 | G | A | 3 | a0001c0012t0001g0089 a0004c0006t0001g0008 a0004c0006t0001g0009 |
3 | HG01168.hp1 HG01169.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.12-1251G>A | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 2/10 | chrX | 3070775 | |||||||
chrX:3070917 | T | TA | 2 | a0004c0006t0001g0008 a0004c0006t0001g0009 |
2 | HG01168.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.12-1108dupA | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chrX | 3070917 | ||||||
chrX:3070938 | G | GGT | 20 | a0001c0001t0001g0035 a0001c0001t0001g0041 a0001c0001t0001g0046 others(17): Show |
20 | HG01070.hp1 HG01071.hp2 HG01109.hp1 others(17): Show |
intron_variant | MODIFIER | c.12-1055_12-1054dup others(2): Show |
ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chrX | 3070938 | ||||||
chrX:3070938 | G | GGTGT | 5 | a0001c0001t0001g0036 a0001c0001t0001g0037 a0001c0001t0001g0038 others(2): Show |
5 | HG02451.hp1 HG02895.hp1 HG02897.hp2 others(2): Show |
intron_variant | MODIFIER | c.12-1057_12-1054dup others(4): Show |
ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chrX | 3070938 | ||||||
chrX:3070938 | GGT | G | 133 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(130): Show |
139 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(136): Show |
intron_variant | MODIFIER | c.12-1055_12-1054del others(2): Show |
ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chrX | 3070938 | ||||||
chrX:3070938 | GGTGTGT | G | 5 | a0001c0001t0001g0032 a0001c0001t0001g0047 a0001c0007t0003g0031 others(2): Show |
5 | HG00738.hp1 HG02257.hp2 HG02965.hp1 others(2): Show |
intron_variant | MODIFIER | c.12-1059_12-1054del others(6): Show |
ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chrX | 3070938 | ||||||
chrX:3070994 | GGATA | G | 145 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(142): Show |
152 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(149): Show |
intron_variant | MODIFIER | c.12-1023_12-1020del others(4): Show |
ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chrX | 3070994 | ||||||
chrX:3071099 | C | T | 15 | a0001c0001t0001g0035 a0001c0001t0001g0036 a0001c0001t0001g0037 others(12): Show |
15 | HG01070.hp1 HG01071.hp2 HG01109.hp1 others(12): Show |
intron_variant | MODIFIER | c.12-927C>T | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 2/10 | chrX | 3071099 | |||||||
chrX:3071193 | T | C | 1 | a0001c0002t0001g0015 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.12-833T>C | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 2/10 | chrX | 3071193 | |||||||
chrX:3071249 | A | G | 20 | a0001c0001t0001g0032 a0001c0001t0001g0035 a0001c0001t0001g0036 others(17): Show |
20 | HG01070.hp1 HG01071.hp2 HG01109.hp1 others(17): Show |
intron_variant | MODIFIER | c.12-777A>G | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 2/10 | chrX | 3071249 | |||||||
chrX:3071291 | T | TTTG | 4 | a0001c0001t0001g0057 a0001c0001t0001g0058 a0001c0001t0001g0059 others(1): Show |
4 | HG01069.hp1 HG01071.hp1 HG01358.hp1 others(1): Show |
intron_variant | MODIFIER | c.12-708_12-706dupGT others(1): Show |
ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chrX | 3071291 | ||||||
chrX:3071425 | C | T | 2 | a0004c0006t0001g0008 a0004c0006t0001g0009 |
2 | HG01168.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.12-601C>T | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 2/10 | chrX | 3071425 | |||||||
chrX:3071599 | C | T | 2 | a0004c0006t0001g0008 a0004c0006t0001g0009 |
2 | HG01168.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.12-427C>T | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 2/10 | chrX | 3071599 | |||||||
chrX:3071643 | G | T | 4 | a0001c0001t0001g0032 a0001c0007t0003g0031 a0001c0007t0003g0182 others(1): Show |
4 | HG02257.hp2 HG02965.hp1 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.12-383G>T | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 2/10 | chrX | 3071643 | |||||||
chrX:3071677 | A | G | 7 | a0001c0001t0001g0032 a0001c0007t0003g0031 a0001c0007t0003g0182 others(4): Show |
7 | HG01168.hp1 HG01169.hp2 HG02257.hp2 others(4): Show |
intron_variant | MODIFIER | c.12-349A>G | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 2/10 | chrX | 3071677 | |||||||
chrX:3072220 | G | C | 4 | a0001c0001t0001g0032 a0001c0007t0003g0031 a0001c0007t0003g0182 others(1): Show |
4 | HG02257.hp2 HG02965.hp1 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.161+45G>C | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 3/10 | chrX | 3072220 | |||||||
chrX:3072269 | T | C | 15 | a0001c0001t0001g0035 a0001c0001t0001g0036 a0001c0001t0001g0037 others(12): Show |
15 | HG01070.hp1 HG01071.hp2 HG01109.hp1 others(12): Show |
intron_variant | MODIFIER | c.161+94T>C | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 3/10 | chrX | 3072269 | |||||||
chrX:3072279 | C | CT | 21 | a0001c0001t0001g0032 a0001c0001t0001g0035 a0001c0001t0001g0036 others(18): Show |
21 | HG01070.hp1 HG01071.hp2 HG01109.hp1 others(18): Show |
intron_variant | MODIFIER | c.161+112dupT | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chrX | 3072279 | ||||||
chrX:3072578 | A | G | 2 | a0004c0006t0001g0008 a0004c0006t0001g0009 |
2 | HG01168.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.161+403A>G | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 3/10 | chrX | 3072578 | |||||||
chrX:3072634 | G | C | 2 | a0004c0006t0001g0008 a0004c0006t0001g0009 |
2 | HG01168.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.161+459G>C | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 3/10 | chrX | 3072634 | |||||||
chrX:3072742 | T | C | 1 | a0001c0012t0001g0089 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.161+567T>C | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 3/10 | chrX | 3072742 | |||||||
chrX:3072849 | A | C | 15 | a0001c0001t0001g0035 a0001c0001t0001g0036 a0001c0001t0001g0037 others(12): Show |
15 | HG01070.hp1 HG01071.hp2 HG01109.hp1 others(12): Show |
intron_variant | MODIFIER | c.161+674A>C | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 3/10 | chrX | 3072849 | |||||||
chrX:3072884 | C | T | 2 | a0004c0006t0001g0008 a0004c0006t0001g0009 |
2 | HG01168.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.161+709C>T | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 3/10 | chrX | 3072884 | |||||||
chrX:3072952 | A | G | 2 | a0004c0006t0001g0008 a0004c0006t0001g0009 |
2 | HG01168.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.161+777A>G | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 3/10 | chrX | 3072952 | |||||||
chrX:3072963 | C | T | 2 | a0004c0006t0001g0008 a0004c0006t0001g0009 |
2 | HG01168.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.161+788C>T | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 3/10 | chrX | 3072963 | |||||||
chrX:3073033 | T | A | 2 | a0004c0006t0001g0008 a0004c0006t0001g0009 |
2 | HG01168.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.161+858T>A | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 3/10 | chrX | 3073033 | |||||||
chrX:3073072 | C | T | 2 | a0001c0007t0003g0031 a0001c0007t0003g0182 |
2 | HG02257.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.161+897C>T | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 3/10 | chrX | 3073072 | |||||||
chrX:3073096 | G | C | 2 | a0004c0006t0001g0008 a0004c0006t0001g0009 |
2 | HG01168.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.161+921G>C | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 3/10 | chrX | 3073096 | |||||||
chrX:3073237 | TTA | T | 65 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(62): Show |
69 | HG00099.hp2 HG00323.hp2 HG00609.hp1 others(66): Show |
intron_variant | MODIFIER | c.161+1071_161+1072d others(4): Show |
ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chrX | 3073237 | ||||||
chrX:3073273 | A | G | 3 | a0001c0002t0001g0014 a0001c0002t0001g0028 a0001c0002t0001g0030 |
3 | HG00642.hp1 HG00735.hp1 HG03688.hp1 |
intron_variant | MODIFIER | c.161+1098A>G | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 3/10 | chrX | 3073273 | |||||||
chrX:3073356 | T | C | 2 | a0004c0006t0001g0008 a0004c0006t0001g0009 |
2 | HG01168.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.161+1181T>C | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 3/10 | chrX | 3073356 | |||||||
chrX:3073531 | T | G | 21 | a0001c0001t0001g0032 a0001c0001t0001g0035 a0001c0001t0001g0036 others(18): Show |
21 | HG01070.hp1 HG01071.hp2 HG01109.hp1 others(18): Show |
intron_variant | MODIFIER | c.161+1356T>G | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 3/10 | chrX | 3073531 | |||||||
chrX:3073533 | A | ATATAGTA others(128): Show |
2 | a0004c0006t0001g0008 a0004c0006t0001g0009 |
2 | HG01168.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.161+1358_161+1359i others(137): Show |
ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 3/10 | chrX | 3073533 | |||||||
chrX:3073533 | A | ATATAGTA others(86): Show |
2 | a0002c0004t0001g0179 a0002c0004t0001g0180 |
2 | HG01070.hp1 HG01071.hp2 |
intron_variant | MODIFIER | c.161+1358_161+1359i others(95): Show |
ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 3/10 | chrX | 3073533 | |||||||
chrX:3073533 | A | ATATAGTA others(144): Show |
1 | a0001c0001t0001g0032 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.161+1358_161+1359i others(153): Show |
ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 3/10 | chrX | 3073533 | |||||||
chrX:3073533 | A | ATATAGTA others(93): Show |
12 | a0001c0001t0001g0035 a0001c0001t0001g0036 a0001c0001t0001g0037 others(9): Show |
12 | HG01109.hp1 HG02280.hp1 HG02451.hp1 others(9): Show |
intron_variant | MODIFIER | c.161+1358_161+1359i others(102): Show |
ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 3/10 | chrX | 3073533 | |||||||
chrX:3073533 | A | ATATAGTA others(100): Show |
1 | a0001c0001t0001g0039 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.161+1358_161+1359i others(109): Show |
ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 3/10 | chrX | 3073533 | |||||||
chrX:3073533 | A | ATATAGTA others(158): Show |
1 | a0002c0003t0001g0050 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.161+1358_161+1359i others(167): Show |
ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 3/10 | chrX | 3073533 | |||||||
chrX:3073533 | A | ATATAGTA others(172): Show |
2 | a0001c0007t0003g0031 a0001c0007t0003g0182 |
2 | HG02257.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.161+1358_161+1359i others(181): Show |
ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 3/10 | chrX | 3073533 | |||||||
chrX:3073536 | A | T | 21 | a0001c0001t0001g0032 a0001c0001t0001g0035 a0001c0001t0001g0036 others(18): Show |
21 | HG01070.hp1 HG01071.hp2 HG01109.hp1 others(18): Show |
intron_variant | MODIFIER | c.161+1361A>T | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 3/10 | chrX | 3073536 | |||||||
chrX:3073545 | T | C | 21 | a0001c0001t0001g0032 a0001c0001t0001g0035 a0001c0001t0001g0036 others(18): Show |
21 | HG01070.hp1 HG01071.hp2 HG01109.hp1 others(18): Show |
intron_variant | MODIFIER | c.161+1370T>C | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 3/10 | chrX | 3073545 | |||||||
chrX:3073585 | A | ATATTTAT others(39): Show |
2 | a0004c0006t0001g0008 a0004c0006t0001g0009 |
2 | HG01168.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.161+1415_161+1416i others(48): Show |
ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chrX | 3073585 | ||||||
chrX:3073669 | A | AAT | 2 | a0004c0006t0001g0008 a0004c0006t0001g0009 |
2 | HG01168.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.161+1500_161+1501d others(4): Show |
ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chrX | 3073669 | ||||||
chrX:3073680 | A | AATAAATA others(27): Show |
1 | a0001c0001t0001g0100 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.161+1520_161+1553d others(36): Show |
ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chrX | 3073680 | ||||||
chrX:3073680 | A | AATAAATA others(129): Show |
2 | a0004c0006t0001g0008 a0004c0006t0001g0009 |
2 | HG01168.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.161+1553_161+1554i others(138): Show |
ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chrX | 3073680 | ||||||
chrX:3073713 | A | T | 1 | a0001c0001t0001g0078 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.161+1538A>T | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 3/10 | chrX | 3073713 | |||||||
chrX:3073751 | A | ATATT | 2 | a0004c0006t0001g0008 a0004c0006t0001g0009 |
2 | HG01168.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.161+1579_161+1580i others(6): Show |
ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chrX | 3073751 | ||||||
chrX:3073826 | T | C | 1 | a0001c0001t0001g0103 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.161+1651T>C | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 3/10 | chrX | 3073826 | |||||||
chrX:3073998 | G | A | 19 | a0001c0001t0001g0032 a0001c0001t0001g0035 a0001c0001t0001g0036 others(16): Show |
19 | HG01070.hp1 HG01071.hp2 HG01109.hp1 others(16): Show |
intron_variant | MODIFIER | c.161+1823G>A | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 3/10 | chrX | 3073998 | |||||||
chrX:3074101 | C | T | 2 | a0001c0007t0003g0031 a0001c0007t0003g0182 |
2 | HG02257.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.161+1926C>T | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 3/10 | chrX | 3074101 | |||||||
chrX:3074148 | G | C | 21 | a0001c0001t0001g0032 a0001c0001t0001g0035 a0001c0001t0001g0036 others(18): Show |
21 | HG01070.hp1 HG01071.hp2 HG01109.hp1 others(18): Show |
intron_variant | MODIFIER | c.161+1973G>C | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 3/10 | chrX | 3074148 | |||||||
chrX:3074436 | C | G | 5 | a0001c0001t0001g0001 a0001c0001t0001g0047 a0001c0001t0001g0048 others(2): Show |
6 | HG00738.hp1 HG01256.hp1 HG01952.hp1 others(3): Show |
intron_variant | MODIFIER | c.162-2112C>G | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 3/10 | chrX | 3074436 | |||||||
chrX:3074586 | T | C | 21 | a0001c0001t0001g0032 a0001c0001t0001g0035 a0001c0001t0001g0036 others(18): Show |
21 | HG01070.hp1 HG01071.hp2 HG01109.hp1 others(18): Show |
intron_variant | MODIFIER | c.162-1962T>C | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 3/10 | chrX | 3074586 | |||||||
chrX:3074809 | C | T | 22 | a0001c0001t0001g0032 a0001c0001t0001g0035 a0001c0001t0001g0036 others(19): Show |
22 | HG01070.hp1 HG01071.hp2 HG01109.hp1 others(19): Show |
intron_variant | MODIFIER | c.162-1739C>T | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 3/10 | chrX | 3074809 | |||||||
chrX:3074856 | C | T | 22 | a0001c0001t0001g0032 a0001c0001t0001g0035 a0001c0001t0001g0036 others(19): Show |
22 | HG01070.hp1 HG01071.hp2 HG01109.hp1 others(19): Show |
intron_variant | MODIFIER | c.162-1692C>T | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 3/10 | chrX | 3074856 | |||||||
chrX:3074869 | G | C | 22 | a0001c0001t0001g0032 a0001c0001t0001g0035 a0001c0001t0001g0036 others(19): Show |
22 | HG01070.hp1 HG01071.hp2 HG01109.hp1 others(19): Show |
intron_variant | MODIFIER | c.162-1679G>C | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 3/10 | chrX | 3074869 | |||||||
chrX:3075070 | C | T | 22 | a0001c0001t0001g0032 a0001c0001t0001g0035 a0001c0001t0001g0036 others(19): Show |
22 | HG01070.hp1 HG01071.hp2 HG01109.hp1 others(19): Show |
intron_variant | MODIFIER | c.162-1478C>T | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 3/10 | chrX | 3075070 | |||||||
chrX:3075101 | G | A | 1 | a0001c0001t0001g0071 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.162-1447G>A | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 3/10 | chrX | 3075101 | |||||||
chrX:3075450 | T | C | 1 | a0001c0001t0001g0054 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.162-1098T>C | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 3/10 | chrX | 3075450 | |||||||
chrX:3075451 | G | A | 1 | a0001c0001t0001g0165 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.162-1097G>A | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 3/10 | chrX | 3075451 | |||||||
chrX:3075488 | G | GTC | 176 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(173): Show |
183 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(180): Show |
intron_variant | MODIFIER | c.162-1056_162-1055d others(4): Show |
ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chrX | 3075488 | ||||||
chrX:3075741 | G | T | 144 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(141): Show |
151 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(148): Show |
intron_variant | MODIFIER | c.162-807G>T | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 3/10 | chrX | 3075741 | |||||||
chrX:3075746 | T | C | 1 | a0001c0012t0001g0089 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.162-802T>C | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 3/10 | chrX | 3075746 | |||||||
chrX:3075897 | CTCTG | C | 148 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(145): Show |
155 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(152): Show |
intron_variant | MODIFIER | c.162-649_162-646del others(4): Show |
ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chrX | 3075897 | ||||||
chrX:3075943 | G | A | 15 | a0001c0001t0001g0035 a0001c0001t0001g0036 a0001c0001t0001g0037 others(12): Show |
15 | HG01070.hp1 HG01071.hp2 HG01109.hp1 others(12): Show |
intron_variant | MODIFIER | c.162-605G>A | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 3/10 | chrX | 3075943 | |||||||
chrX:3075983 | G | GTC | 148 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(145): Show |
155 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(152): Show |
intron_variant | MODIFIER | c.162-561_162-560dup others(2): Show |
ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chrX | 3075983 | ||||||
chrX:3076105 | TTCTC | T | 2 | a0001c0001t0001g0148 a0001c0001t0001g0186 |
2 | HG03669.hp1 NA19063.hp1 |
intron_variant | MODIFIER | c.162-435_162-432del others(4): Show |
ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chrX | 3076105 | ||||||
chrX:3076113 | CTCTG | C | 2 | a0001c0001t0001g0107 a0001c0001t0001g0108 |
2 | NA18955.hp1 NA19085.hp1 |
intron_variant | MODIFIER | c.162-431_162-428del others(4): Show |
ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chrX | 3076113 | ||||||
chrX:3076336 | GTC | G | 149 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(146): Show |
156 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(153): Show |
intron_variant | MODIFIER | c.162-200_162-199del others(2): Show |
ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chrX | 3076336 | ||||||
chrX:3076386 | C | G | 1 | a0001c0001t0001g0019 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.162-162C>G | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 3/10 | chrX | 3076386 | |||||||
chrX:3076393 | T | C | 150 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(147): Show |
157 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(154): Show |
intron_variant | MODIFIER | c.162-155T>C | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 3/10 | chrX | 3076393 | |||||||
chrX:3076394 | G | A | 1 | a0001c0001t0001g0093 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.162-154G>A | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 3/10 | chrX | 3076394 | |||||||
chrX:3076509 | T | C | 4 | a0001c0001t0001g0032 a0001c0007t0003g0031 a0001c0007t0003g0182 others(1): Show |
4 | HG02257.hp2 HG02965.hp1 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.162-39T>C | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 3/10 | chrX | 3076509 | |||||||
chrX:3076684 | G | A | 8 | a0001c0001t0001g0081 a0001c0001t0001g0082 a0001c0001t0001g0083 others(5): Show |
8 | HG02071.hp1 NA18612.hp1 NA18952.hp1 others(5): Show |
intron_variant | MODIFIER | c.283+15G>A | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 4/10 | chrX | 3076684 | |||||||
chrX:3076702 | C | T | 1 | a0002c0003t0001g0050 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.283+33C>T | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 4/10 | chrX | 3076702 | |||||||
chrX:3076770 | C | T | 1 | a0001c0002t0001g0022 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.283+101C>T | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 4/10 | chrX | 3076770 | |||||||
chrX:3076803 | G | A | 3 | a0002c0004t0001g0090 a0002c0004t0001g0179 a0002c0004t0001g0180 |
3 | HG01070.hp1 HG01071.hp2 HG02622.hp1 |
intron_variant | MODIFIER | c.283+134G>A | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 4/10 | chrX | 3076803 | |||||||
chrX:3076855 | G | C | 1 | a0001c0001t0001g0056 | 1 | NA19072.hp1 | intron_variant | MODIFIER | c.283+186G>C | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 4/10 | chrX | 3076855 | |||||||
chrX:3076892 | T | A | 3 | a0001c0001t0001g0032 a0001c0007t0003g0031 a0001c0007t0003g0182 |
3 | HG02257.hp2 HG02965.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.283+223T>A | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 4/10 | chrX | 3076892 | |||||||
chrX:3077036 | G | A | 144 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(141): Show |
151 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(148): Show |
intron_variant | MODIFIER | c.283+367G>A | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 4/10 | chrX | 3077036 | |||||||
chrX:3077375 | A | G | 3 | a0004c0006t0001g0008 a0004c0006t0001g0009 a0004c0006t0001g0130 |
3 | HG01168.hp1 HG01169.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.283+706A>G | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 4/10 | chrX | 3077375 | |||||||
chrX:3077456 | C | A | 3 | a0004c0006t0001g0008 a0004c0006t0001g0009 a0004c0006t0001g0130 |
3 | HG01168.hp1 HG01169.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.283+787C>A | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 4/10 | chrX | 3077456 | |||||||
chrX:3077554 | G | A | 145 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(142): Show |
152 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(149): Show |
intron_variant | MODIFIER | c.283+885G>A | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 4/10 | chrX | 3077554 | |||||||
chrX:3077788 | A | T | 1 | a0001c0005t0001g0043 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.283+1119A>T | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 4/10 | chrX | 3077788 | |||||||
chrX:3077789 | T | TATTATTA others(3): Show |
1 | a0001c0005t0001g0043 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.283+1120_283+1121i others(12): Show |
ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 4/10 | chrX | 3077789 | |||||||
chrX:3077789 | T | TTTATTA | 4 | a0001c0001t0001g0006 a0001c0001t0001g0041 a0001c0001t0001g0157 others(1): Show |
5 | HG01192.hp1 HG02486.hp1 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.283+1144_283+1149d others(8): Show |
ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chrX | 3077789 | ||||||
chrX:3077789 | T | TTTATTAT others(2): Show |
9 | a0001c0001t0001g0079 a0001c0001t0001g0140 a0001c0001t0001g0158 others(6): Show |
9 | HG00099.hp2 HG01074.hp1 HG01168.hp1 others(6): Show |
intron_variant | MODIFIER | c.283+1141_283+1149d others(11): Show |
ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chrX | 3077789 | ||||||
chrX:3077789 | T | TTTATTAT others(5): Show |
39 | a0001c0001t0001g0005 a0001c0001t0001g0007 a0001c0001t0001g0011 others(36): Show |
41 | HG00140.hp1 HG00280.hp1 HG00609.hp1 others(38): Show |
intron_variant | MODIFIER | c.283+1138_283+1149d others(14): Show |
ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chrX | 3077789 | ||||||
chrX:3077789 | T | TTTATTAT others(8): Show |
50 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0052 others(47): Show |
52 | HG00323.hp2 HG00621.hp1 HG01069.hp1 others(49): Show |
intron_variant | MODIFIER | c.283+1135_283+1149d others(17): Show |
ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chrX | 3077789 | ||||||
chrX:3077789 | T | TTTATTAT others(11): Show |
30 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0049 others(27): Show |
32 | HG00597.hp2 HG00735.hp2 HG01070.hp2 others(29): Show |
intron_variant | MODIFIER | c.283+1132_283+1149d others(20): Show |
ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chrX | 3077789 | ||||||
chrX:3077789 | T | TTTATTAT others(14): Show |
12 | a0001c0001t0001g0046 a0001c0001t0001g0047 a0001c0001t0001g0048 others(9): Show |
12 | HG00738.hp1 HG01256.hp1 HG01978.hp2 others(9): Show |
intron_variant | MODIFIER | c.283+1129_283+1149d others(23): Show |
ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chrX | 3077789 | ||||||
chrX:3077789 | T | TTTATTAT others(17): Show |
1 | a0001c0001t0001g0075 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.283+1126_283+1149d others(26): Show |
ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chrX | 3077789 | ||||||
chrX:3077789 | T | TTTTTTAT others(5): Show |
2 | a0001c0001t0001g0091 a0001c0019t0001g0095 |
2 | HG02735.hp1 NA20752.hp1 |
intron_variant | MODIFIER | c.283+1122_283+1123i others(14): Show |
ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chrX | 3077789 | ||||||
chrX:3077857 | T | G | 148 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(145): Show |
155 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(152): Show |
intron_variant | MODIFIER | c.283+1188T>G | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 4/10 | chrX | 3077857 | |||||||
chrX:3078079 | T | C | 152 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(149): Show |
159 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(156): Show |
intron_variant | MODIFIER | c.283+1410T>C | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 4/10 | chrX | 3078079 | |||||||
chrX:3078099 | C | T | 3 | a0001c0001t0001g0032 a0001c0007t0003g0031 a0001c0007t0003g0182 |
3 | HG02257.hp2 HG02965.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.283+1430C>T | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 4/10 | chrX | 3078099 | |||||||
chrX:3078121 | A | G | 145 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(142): Show |
152 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(149): Show |
intron_variant | MODIFIER | c.283+1452A>G | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 4/10 | chrX | 3078121 | |||||||
chrX:3078239 | G | A | 72 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(69): Show |
76 | HG00099.hp2 HG00323.hp2 HG00609.hp1 others(73): Show |
intron_variant | MODIFIER | c.283+1570G>A | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 4/10 | chrX | 3078239 | |||||||
chrX:3078418 | G | A | 145 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(142): Show |
152 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(149): Show |
intron_variant | MODIFIER | c.283+1749G>A | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 4/10 | chrX | 3078418 | |||||||
chrX:3078648 | C | T | 3 | a0004c0006t0001g0008 a0004c0006t0001g0009 a0004c0006t0001g0130 |
3 | HG01168.hp1 HG01169.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.283+1979C>T | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 4/10 | chrX | 3078648 | |||||||
chrX:3078653 | C | T | 3 | a0004c0006t0001g0008 a0004c0006t0001g0009 a0004c0006t0001g0130 |
3 | HG01168.hp1 HG01169.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.283+1984C>T | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 4/10 | chrX | 3078653 | |||||||
chrX:3078951 | C | T | 3 | a0004c0006t0001g0008 a0004c0006t0001g0009 a0004c0006t0001g0130 |
3 | HG01168.hp1 HG01169.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.284-1940C>T | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 4/10 | chrX | 3078951 | |||||||
chrX:3079028 | C | T | 145 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(142): Show |
152 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(149): Show |
intron_variant | MODIFIER | c.284-1863C>T | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 4/10 | chrX | 3079028 | |||||||
chrX:3079342 | AT | A | 5 | a0001c0001t0001g0110 a0001c0001t0001g0111 a0001c0001t0001g0112 others(2): Show |
5 | HG00323.hp1 NA18957.hp1 NA18988.hp1 others(2): Show |
intron_variant | MODIFIER | c.284-1529delT | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chrX | 3079342 | ||||||
chrX:3079342 | ATT | A | 131 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(128): Show |
138 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(135): Show |
intron_variant | MODIFIER | c.284-1530_284-1529d others(4): Show |
ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chrX | 3079342 | ||||||
chrX:3079342 | ATTT | A | 9 | a0001c0001t0001g0053 a0001c0001t0001g0055 a0001c0001t0001g0068 others(6): Show |
9 | HG00140.hp1 HG01255.hp1 HG01258.hp1 others(6): Show |
intron_variant | MODIFIER | c.284-1531_284-1529d others(5): Show |
ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chrX | 3079342 | ||||||
chrX:3079439 | G | A | 1 | a0001c0001t0001g0133 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.284-1452G>A | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 4/10 | chrX | 3079439 | |||||||
chrX:3079462 | A | G | 4 | a0001c0001t0001g0032 a0001c0007t0003g0031 a0001c0007t0003g0182 others(1): Show |
4 | HG02257.hp2 HG02965.hp1 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.284-1429A>G | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 4/10 | chrX | 3079462 | |||||||
chrX:3079533 | G | A | 2 | a0004c0006t0001g0008 a0004c0006t0001g0009 |
2 | HG01168.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.284-1358G>A | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 4/10 | chrX | 3079533 | |||||||
chrX:3079957 | T | TCAA | 3 | a0001c0001t0001g0038 a0001c0001t0001g0039 a0001c0010t0001g0033 |
3 | HG02280.hp1 HG02451.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.284-921_284-919dup others(3): Show |
ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chrX | 3079957 | ||||||
chrX:3079970 | C | A | 1 | a0001c0001t0001g0147 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.284-921C>A | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 4/10 | chrX | 3079970 | |||||||
chrX:3079970 | C | CA | 13 | a0001c0001t0001g0045 a0001c0001t0001g0047 a0001c0001t0001g0054 others(10): Show |
13 | HG00673.hp1 HG00735.hp1 HG00738.hp1 others(10): Show |
intron_variant | MODIFIER | c.284-899dupA | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chrX | 3079970 | ||||||
chrX:3079970 | CA | C | 12 | a0001c0001t0001g0019 a0001c0001t0001g0046 a0001c0001t0001g0049 others(9): Show |
12 | HG01070.hp1 HG01168.hp2 HG01943.hp1 others(9): Show |
intron_variant | MODIFIER | c.284-899delA | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chrX | 3079970 | ||||||
chrX:3079973 | A | C | 2 | a0001c0001t0001g0035 a0001c0010t0001g0040 |
2 | HG02809.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.284-918A>C | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 4/10 | chrX | 3079973 | |||||||
chrX:3079993 | G | A | 2 | a0001c0001t0001g0035 a0001c0010t0001g0040 |
2 | HG02809.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.284-898G>A | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 4/10 | chrX | 3079993 | |||||||
chrX:3080004 | A | AG | 2 | a0001c0001t0001g0035 a0001c0010t0001g0040 |
2 | HG02809.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.284-887_284-886ins others(1): Show |
ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 4/10 | chrX | 3080004 | |||||||
chrX:3080005 | A | G | 152 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(149): Show |
159 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(156): Show |
intron_variant | MODIFIER | c.284-886A>G | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 4/10 | chrX | 3080005 | |||||||
chrX:3080006 | A | G | 3 | a0001c0001t0001g0035 a0001c0010t0001g0033 a0001c0010t0001g0040 |
3 | HG02280.hp1 HG02809.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.284-885A>G | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 4/10 | chrX | 3080006 | |||||||
chrX:3080101 | G | A | 1 | a0001c0001t0001g0121 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.284-790G>A | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 4/10 | chrX | 3080101 | |||||||
chrX:3080186 | T | A | 1 | a0001c0001t0001g0176 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.284-705T>A | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 4/10 | chrX | 3080186 | |||||||
chrX:3080255 | CATGAGGT others(30): Show |
C | 145 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(142): Show |
152 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(149): Show |
intron_variant | MODIFIER | c.284-631_284-595del others(37): Show |
ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chrX | 3080255 | ||||||
chrX:3080265 | G | A | 3 | a0001c0001t0001g0035 a0001c0010t0001g0033 a0001c0010t0001g0040 |
3 | HG02280.hp1 HG02809.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.284-626G>A | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 4/10 | chrX | 3080265 | |||||||
chrX:3080286 | C | T | 3 | a0002c0004t0001g0090 a0002c0004t0001g0179 a0002c0004t0001g0180 |
3 | HG01070.hp1 HG01071.hp2 HG02622.hp1 |
intron_variant | MODIFIER | c.284-605C>T | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 4/10 | chrX | 3080286 | |||||||
chrX:3080358 | C | T | 4 | a0001c0001t0001g0020 a0001c0001t0001g0057 a0001c0001t0001g0058 others(1): Show |
4 | HG00741.hp2 HG01069.hp1 HG01071.hp1 others(1): Show |
intron_variant | MODIFIER | c.284-533C>T | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 4/10 | chrX | 3080358 | |||||||
chrX:3080433 | T | C | 183 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(180): Show |
190 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(187): Show |
intron_variant | MODIFIER | c.284-458T>C | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 4/10 | chrX | 3080433 | |||||||
chrX:3080450 | G | A | 1 | a0001c0015t0006g0021 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.284-441G>A | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 4/10 | chrX | 3080450 | |||||||
chrX:3080459 | C | T | 154 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(151): Show |
161 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(158): Show |
intron_variant | MODIFIER | c.284-432C>T | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 4/10 | chrX | 3080459 | |||||||
chrX:3080472 | C | CA | 149 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(146): Show |
156 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(153): Show |
intron_variant | MODIFIER | c.284-406dupA | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chrX | 3080472 | ||||||
chrX:3080649 | G | A | 3 | a0004c0006t0001g0008 a0004c0006t0001g0009 a0004c0006t0001g0130 |
3 | HG01168.hp1 HG01169.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.284-242G>A | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 4/10 | chrX | 3080649 | |||||||
chrX:3080771 | G | A | 3 | a0004c0006t0001g0008 a0004c0006t0001g0009 a0004c0006t0001g0130 |
3 | HG01168.hp1 HG01169.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.284-120G>A | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 4/10 | chrX | 3080771 | |||||||
chrX:3080855 | A | G | 1 | a0001c0001t0001g0145 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.284-36A>G | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 4/10 | chrX | 3080855 | |||||||
chrX:3081100 | G | A | 159 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(156): Show |
166 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(163): Show |
intron_variant | MODIFIER | c.406+87G>A | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 5/10 | chrX | 3081100 | |||||||
chrX:3081130 | G | A | 1 | a0001c0002t0001g0128 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.406+117G>A | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 5/10 | chrX | 3081130 | |||||||
chrX:3081460 | T | C | 159 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(156): Show |
166 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(163): Show |
intron_variant | MODIFIER | c.406+447T>C | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 5/10 | chrX | 3081460 | |||||||
chrX:3081481 | C | T | 3 | a0001c0001t0001g0061 a0001c0001t0001g0126 a0001c0001t0001g0127 |
3 | HG01099.hp1 HG01496.hp1 HG01978.hp1 |
intron_variant | MODIFIER | c.406+468C>T | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 5/10 | chrX | 3081481 | |||||||
chrX:3081493 | C | T | 3 | a0001c0001t0001g0035 a0001c0010t0001g0033 a0001c0010t0001g0040 |
3 | HG02280.hp1 HG02809.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.406+480C>T | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 5/10 | chrX | 3081493 | |||||||
chrX:3081807 | A | G | 1 | a0001c0001t0001g0105 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.406+794A>G | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 5/10 | chrX | 3081807 | |||||||
chrX:3082125 | A | G | 6 | a0001c0001t0001g0035 a0001c0010t0001g0033 a0001c0010t0001g0040 others(3): Show |
6 | HG01168.hp1 HG01169.hp2 HG02280.hp1 others(3): Show |
intron_variant | MODIFIER | c.406+1112A>G | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 5/10 | chrX | 3082125 | |||||||
chrX:3082133 | C | T | 3 | a0004c0006t0001g0008 a0004c0006t0001g0009 a0004c0006t0001g0130 |
3 | HG01168.hp1 HG01169.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.406+1120C>T | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 5/10 | chrX | 3082133 | |||||||
chrX:3082346 | C | A | 1 | a0001c0001t0001g0147 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.406+1333C>A | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 5/10 | chrX | 3082346 | |||||||
chrX:3082698 | C | A | 1 | a0001c0001t0001g0094 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.407-1545C>A | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 5/10 | chrX | 3082698 | |||||||
chrX:3082960 | CTATCT | C | 6 | a0001c0001t0001g0035 a0001c0010t0001g0033 a0001c0010t0001g0040 others(3): Show |
6 | HG01168.hp1 HG01169.hp2 HG02280.hp1 others(3): Show |
intron_variant | MODIFIER | c.407-1277_407-1273d others(7): Show |
ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chrX | 3082960 | ||||||
chrX:3082965 | T | G | 3 | a0002c0004t0001g0090 a0002c0004t0001g0179 a0002c0004t0001g0180 |
3 | HG01070.hp1 HG01071.hp2 HG02622.hp1 |
intron_variant | MODIFIER | c.407-1278T>G | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 5/10 | chrX | 3082965 | |||||||
chrX:3083023 | TTATC | T | 3 | a0004c0006t0001g0008 a0004c0006t0001g0009 a0004c0006t0001g0130 |
3 | HG01168.hp1 HG01169.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.407-1211_407-1208d others(6): Show |
ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chrX | 3083023 | ||||||
chrX:3083064 | ATATC | A | 5 | a0001c0001t0001g0035 a0001c0001t0001g0038 a0001c0001t0001g0039 others(2): Show |
5 | HG02280.hp1 HG02451.hp1 HG02809.hp1 others(2): Show |
intron_variant | MODIFIER | c.407-1163_407-1160d others(6): Show |
ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chrX | 3083064 | ||||||
chrX:3083225 | A | G | 1 | a0002c0003t0001g0050 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.407-1018A>G | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 5/10 | chrX | 3083225 | |||||||
chrX:3083388 | C | G | 1 | a0001c0001t0001g0068 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.407-855C>G | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 5/10 | chrX | 3083388 | |||||||
chrX:3083404 | C | A | 3 | a0001c0001t0001g0035 a0001c0010t0001g0033 a0001c0010t0001g0040 |
3 | HG02280.hp1 HG02809.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.407-839C>A | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 5/10 | chrX | 3083404 | |||||||
chrX:3083440 | G | A | 3 | a0004c0006t0001g0008 a0004c0006t0001g0009 a0004c0006t0001g0130 |
3 | HG01168.hp1 HG01169.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.407-803G>A | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 5/10 | chrX | 3083440 | |||||||
chrX:3083481 | CCTAT | C | 13 | a0001c0002t0001g0014 a0001c0002t0001g0015 a0001c0002t0001g0024 others(10): Show |
13 | HG00323.hp1 HG00735.hp1 HG01109.hp1 others(10): Show |
intron_variant | MODIFIER | c.407-716_407-713del others(4): Show |
ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chrX | 3083481 | ||||||
chrX:3083481 | CCTATCTA others(1): Show |
C | 3 | a0001c0002t0001g0028 a0001c0002t0001g0128 a0002c0003t0001g0106 |
3 | HG00642.hp1 HG02083.hp1 HG02300.hp1 |
intron_variant | MODIFIER | c.407-720_407-713del others(8): Show |
ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chrX | 3083481 | ||||||
chrX:3083481 | CCTATCTA others(5): Show |
C | 1 | a0001c0002t0001g0022 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.407-724_407-713del others(12): Show |
ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chrX | 3083481 | ||||||
chrX:3083511 | TATCTATC others(13): Show |
T | 1 | a0001c0001t0001g0178 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.407-728_407-709del others(20): Show |
ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chrX | 3083511 | ||||||
chrX:3083515 | TATCTATC others(9): Show |
T | 2 | a0001c0001t0001g0096 a0004c0006t0001g0130 |
2 | HG01978.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.407-724_407-709del others(16): Show |
ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chrX | 3083515 | ||||||
chrX:3083519 | TATCTATC others(5): Show |
T | 28 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0011 others(25): Show |
29 | HG00140.hp1 HG00673.hp1 HG00735.hp2 others(26): Show |
intron_variant | MODIFIER | c.407-720_407-709del others(12): Show |
ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chrX | 3083519 | ||||||
chrX:3083523 | TATCTATC others(1): Show |
T | 108 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(105): Show |
111 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(108): Show |
intron_variant | MODIFIER | c.407-716_407-709del others(8): Show |
ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chrX | 3083523 | ||||||
chrX:3083527 | TATCC | T | 18 | a0001c0001t0001g0005 a0001c0001t0001g0039 a0001c0001t0001g0053 others(15): Show |
18 | HG01255.hp1 HG01258.hp1 HG02015.hp1 others(15): Show |
intron_variant | MODIFIER | c.407-698_407-695del others(4): Show |
ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chrX | 3083527 | ||||||
chrX:3083531 | C | T | 5 | a0001c0001t0001g0004 a0001c0001t0001g0084 a0001c0001t0001g0087 others(2): Show |
5 | NA18612.hp1 NA18971.hp1 NA18974.hp1 others(2): Show |
intron_variant | MODIFIER | c.407-712C>T | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 5/10 | chrX | 3083531 | |||||||
chrX:3083851 | C | T | 6 | a0001c0001t0001g0035 a0001c0010t0001g0033 a0001c0010t0001g0040 others(3): Show |
6 | HG01168.hp1 HG01169.hp2 HG02280.hp1 others(3): Show |
intron_variant | MODIFIER | c.407-392C>T | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 5/10 | chrX | 3083851 | |||||||
chrX:3083884 | C | T | 3 | a0004c0006t0001g0008 a0004c0006t0001g0009 a0004c0006t0001g0130 |
3 | HG01168.hp1 HG01169.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.407-359C>T | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 5/10 | chrX | 3083884 | |||||||
chrX:3084079 | G | A | 3 | a0004c0006t0001g0008 a0004c0006t0001g0009 a0004c0006t0001g0130 |
3 | HG01168.hp1 HG01169.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.407-164G>A | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 5/10 | chrX | 3084079 | |||||||
chrX:3084178 | T | C | 159 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(156): Show |
166 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(163): Show |
intron_variant | MODIFIER | c.407-65T>C | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 5/10 | chrX | 3084178 | |||||||
chrX:3084904 | A | T | 1 | a0006c0014t0002g0025 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.830+238A>T | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 6/10 | chrX | 3084904 | |||||||
chrX:3085097 | C | T | 3 | a0004c0006t0001g0008 a0004c0006t0001g0009 a0004c0006t0001g0130 |
3 | HG01168.hp1 HG01169.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.830+431C>T | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 6/10 | chrX | 3085097 | |||||||
chrX:3085120 | T | C | 3 | a0004c0006t0001g0008 a0004c0006t0001g0009 a0004c0006t0001g0130 |
3 | HG01168.hp1 HG01169.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.830+454T>C | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 6/10 | chrX | 3085120 | |||||||
chrX:3085217 | G | A | 2 | a0001c0001t0001g0038 a0001c0001t0001g0039 |
2 | HG02451.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.830+551G>A | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 6/10 | chrX | 3085217 | |||||||
chrX:3085261 | G | A | 8 | a0001c0001t0001g0081 a0001c0001t0001g0082 a0001c0001t0001g0083 others(5): Show |
8 | HG02071.hp1 NA18612.hp1 NA18952.hp1 others(5): Show |
intron_variant | MODIFIER | c.830+595G>A | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 6/10 | chrX | 3085261 | |||||||
chrX:3085302 | G | GTA | 3 | a0001c0001t0001g0035 a0001c0010t0001g0033 a0001c0010t0001g0040 |
3 | HG02280.hp1 HG02809.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.830+645_830+646dup others(2): Show |
ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chrX | 3085302 | ||||||
chrX:3085360 | A | T | 156 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(153): Show |
163 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(160): Show |
intron_variant | MODIFIER | c.830+694A>T | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 6/10 | chrX | 3085360 | |||||||
chrX:3085541 | T | C | 3 | a0004c0006t0001g0008 a0004c0006t0001g0009 a0004c0006t0001g0130 |
3 | HG01168.hp1 HG01169.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.830+875T>C | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 6/10 | chrX | 3085541 | |||||||
chrX:3085646 | AT | A | 3 | a0001c0001t0001g0035 a0001c0010t0001g0033 a0001c0010t0001g0040 |
3 | HG02280.hp1 HG02809.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.830+986delT | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chrX | 3085646 | ||||||
chrX:3085853 | A | T | 3 | a0001c0001t0001g0035 a0001c0010t0001g0033 a0001c0010t0001g0040 |
3 | HG02280.hp1 HG02809.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.830+1187A>T | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 6/10 | chrX | 3085853 | |||||||
chrX:3086116 | C | T | 2 | a0001c0001t0001g0138 a0001c0001t0001g0140 |
2 | HG01517.hp1 HG02257.hp1 |
intron_variant | MODIFIER | c.830+1450C>T | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 6/10 | chrX | 3086116 | |||||||
chrX:3086580 | G | T | 3 | a0001c0001t0001g0035 a0001c0010t0001g0033 a0001c0010t0001g0040 |
3 | HG02280.hp1 HG02809.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.830+1914G>T | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 6/10 | chrX | 3086580 | |||||||
chrX:3086602 | G | A | 153 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(150): Show |
160 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(157): Show |
intron_variant | MODIFIER | c.830+1936G>A | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 6/10 | chrX | 3086602 | |||||||
chrX:3086627 | G | A | 1 | a0001c0001t0001g0118 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.830+1961G>A | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 6/10 | chrX | 3086627 | |||||||
chrX:3086661 | CA | C | 153 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(150): Show |
160 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(157): Show |
intron_variant | MODIFIER | c.830+2002delA | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chrX | 3086661 | ||||||
chrX:3086817 | T | C | 3 | a0001c0001t0001g0035 a0001c0010t0001g0033 a0001c0010t0001g0040 |
3 | HG02280.hp1 HG02809.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.830+2151T>C | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 6/10 | chrX | 3086817 | |||||||
chrX:3086850 | G | A | 1 | a0002c0003t0001g0050 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.830+2184G>A | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 6/10 | chrX | 3086850 | |||||||
chrX:3087201 | G | T | 159 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(156): Show |
166 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(163): Show |
intron_variant | MODIFIER | c.831-2295G>T | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 6/10 | chrX | 3087201 | |||||||
chrX:3087369 | C | T | 4 | a0001c0001t0001g0019 a0001c0001t0001g0091 a0001c0001t0001g0157 others(1): Show |
4 | HG01168.hp2 HG01192.hp1 HG02735.hp1 others(1): Show |
intron_variant | MODIFIER | c.831-2127C>T | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 6/10 | chrX | 3087369 | |||||||
chrX:3087636 | G | T | 3 | a0001c0001t0001g0035 a0001c0010t0001g0033 a0001c0010t0001g0040 |
3 | HG02280.hp1 HG02809.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.831-1860G>T | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 6/10 | chrX | 3087636 | |||||||
chrX:3087649 | A | T | 3 | a0001c0001t0001g0035 a0001c0010t0001g0033 a0001c0010t0001g0040 |
3 | HG02280.hp1 HG02809.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.831-1847A>T | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 6/10 | chrX | 3087649 | |||||||
chrX:3087703 | G | T | 1 | a0001c0001t0001g0127 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.831-1793G>T | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 6/10 | chrX | 3087703 | |||||||
chrX:3087764 | C | T | 3 | a0001c0001t0001g0035 a0001c0010t0001g0033 a0001c0010t0001g0040 |
3 | HG02280.hp1 HG02809.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.831-1732C>T | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 6/10 | chrX | 3087764 | |||||||
chrX:3087826 | T | A | 1 | a0006c0014t0002g0025 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.831-1670T>A | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 6/10 | chrX | 3087826 | |||||||
chrX:3088086 | A | G | 3 | a0004c0006t0001g0008 a0004c0006t0001g0009 a0004c0006t0001g0130 |
3 | HG01168.hp1 HG01169.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.831-1410A>G | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 6/10 | chrX | 3088086 | |||||||
chrX:3088209 | G | A | 1 | a0001c0001t0001g0087 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.831-1287G>A | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 6/10 | chrX | 3088209 | |||||||
chrX:3088310 | T | A | 1 | a0002c0003t0001g0050 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.831-1186T>A | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 6/10 | chrX | 3088310 | |||||||
chrX:3088564 | CT | C | 161 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(158): Show |
168 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(165): Show |
intron_variant | MODIFIER | c.831-917delT | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chrX | 3088564 | ||||||
chrX:3089162 | A | G | 1 | a0007c0021t0001g0174 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.831-334A>G | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 6/10 | chrX | 3089162 | |||||||
chrX:3089236 | C | G | 7 | a0001c0002t0001g0181 a0001c0002t0001g0183 a0001c0002t0001g0184 others(4): Show |
7 | HG01109.hp1 HG02257.hp2 HG02622.hp2 others(4): Show |
intron_variant | MODIFIER | c.831-260C>G | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 6/10 | chrX | 3089236 | |||||||
chrX:3089439 | G | T | 156 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(153): Show |
163 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(160): Show |
intron_variant | MODIFIER | c.831-57G>T | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 6/10 | chrX | 3089439 | |||||||
chrX:3090231 | T | C | 153 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(150): Show |
160 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(157): Show |
intron_variant | MODIFIER | c.967+599T>C | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 7/10 | chrX | 3090231 | |||||||
chrX:3090319 | T | A | 156 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(153): Show |
163 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(160): Show |
intron_variant | MODIFIER | c.967+687T>A | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 7/10 | chrX | 3090319 | |||||||
chrX:3090721 | A | G | 3 | a0001c0001t0001g0035 a0001c0010t0001g0033 a0001c0010t0001g0040 |
3 | HG02280.hp1 HG02809.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.967+1089A>G | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 7/10 | chrX | 3090721 | |||||||
chrX:3091047 | GCTAT | G | 168 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(165): Show |
175 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(172): Show |
intron_variant | MODIFIER | c.967+1420_967+1423d others(6): Show |
ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chrX | 3091047 | ||||||
chrX:3091061 | C | A | 1 | a0001c0002t0001g0030 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.967+1429C>A | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 7/10 | chrX | 3091061 | |||||||
chrX:3091578 | C | A | 3 | a0004c0006t0001g0008 a0004c0006t0001g0009 a0004c0006t0001g0130 |
3 | HG01168.hp1 HG01169.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.967+1946C>A | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 7/10 | chrX | 3091578 | |||||||
chrX:3091642 | T | A | 3 | a0001c0001t0001g0035 a0001c0010t0001g0033 a0001c0010t0001g0040 |
3 | HG02280.hp1 HG02809.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.967+2010T>A | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 7/10 | chrX | 3091642 | |||||||
chrX:3091665 | A | G | 2 | a0001c0001t0001g0005 a0001c0001t0001g0073 |
3 | NA18944.hp1 NA18946.hp2 NA19076.hp1 |
intron_variant | MODIFIER | c.967+2033A>G | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 7/10 | chrX | 3091665 | |||||||
chrX:3091823 | T | TGATA | 166 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(163): Show |
173 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(170): Show |
intron_variant | MODIFIER | c.967+2193_967+2196d others(6): Show |
ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chrX | 3091823 | ||||||
chrX:3091833 | T | C | 1 | a0001c0001t0001g0079 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.967+2201T>C | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 7/10 | chrX | 3091833 | |||||||
chrX:3091885 | C | T | 1 | a0001c0001t0001g0071 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.967+2253C>T | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 7/10 | chrX | 3091885 | |||||||
chrX:3091938 | CAG | C | 2 | a0001c0001t0001g0019 a0001c0001t0001g0157 |
2 | HG01168.hp2 HG01192.hp1 |
intron_variant | MODIFIER | c.967+2308_967+2309d others(4): Show |
ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chrX | 3091938 | ||||||
chrX:3092021 | A | G | 3 | a0002c0004t0001g0090 a0002c0004t0001g0179 a0002c0004t0001g0180 |
3 | HG01070.hp1 HG01071.hp2 HG02622.hp1 |
intron_variant | MODIFIER | c.967+2389A>G | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 7/10 | chrX | 3092021 | |||||||
chrX:3092082 | A | G | 2 | a0001c0005t0001g0010 a0001c0005t0001g0012 |
2 | HG03041.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.967+2450A>G | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 7/10 | chrX | 3092082 | |||||||
chrX:3092167 | T | TGATA | 6 | a0001c0002t0001g0181 a0001c0002t0001g0183 a0001c0002t0001g0185 others(3): Show |
6 | HG01109.hp1 HG02257.hp2 HG02896.hp2 others(3): Show |
intron_variant | MODIFIER | c.967+2544_967+2547d others(6): Show |
ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chrX | 3092167 | ||||||
chrX:3092167 | TGATA | T | 149 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(146): Show |
156 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(153): Show |
intron_variant | MODIFIER | c.967+2544_967+2547d others(6): Show |
ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chrX | 3092167 | ||||||
chrX:3092172 | GATAGATA others(5): Show |
G | 2 | a0001c0001t0001g0038 a0001c0001t0001g0039 |
2 | HG02451.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.967+2544_967+2555d others(14): Show |
ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chrX | 3092172 | ||||||
chrX:3092176 | G | C | 4 | a0001c0001t0001g0036 a0001c0001t0001g0037 a0001c0001t0001g0052 others(1): Show |
4 | HG02055.hp1 HG02895.hp1 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.967+2544G>C | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 7/10 | chrX | 3092176 | |||||||
chrX:3092176 | G | GATAC | 6 | a0001c0002t0001g0015 a0002c0003t0001g0013 a0002c0003t0001g0017 others(3): Show |
6 | HG00597.hp1 HG01167.hp1 HG01169.hp1 others(3): Show |
intron_variant | MODIFIER | c.967+2576_967+2579d others(6): Show |
ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chrX | 3092176 | ||||||
chrX:3092180 | C | G | 3 | a0001c0001t0001g0035 a0001c0010t0001g0033 a0001c0010t0001g0040 |
3 | HG02280.hp1 HG02809.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.967+2548C>G | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 7/10 | chrX | 3092180 | |||||||
chrX:3092184 | C | G | 3 | a0001c0001t0001g0035 a0001c0010t0001g0033 a0001c0010t0001g0040 |
3 | HG02280.hp1 HG02809.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.967+2552C>G | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 7/10 | chrX | 3092184 | |||||||
chrX:3092212 | G | C | 7 | a0001c0002t0001g0181 a0001c0002t0001g0183 a0001c0002t0001g0184 others(4): Show |
7 | HG01109.hp1 HG02257.hp2 HG02622.hp2 others(4): Show |
intron_variant | MODIFIER | c.967+2580G>C | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 7/10 | chrX | 3092212 | |||||||
chrX:3092215 | A | G | 153 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(150): Show |
160 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(157): Show |
intron_variant | MODIFIER | c.967+2583A>G | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 7/10 | chrX | 3092215 | |||||||
chrX:3092371 | C | G | 1 | a0001c0001t0001g0070 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.967+2739C>G | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 7/10 | chrX | 3092371 | |||||||
chrX:3092459 | C | A | 159 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(156): Show |
166 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(163): Show |
intron_variant | MODIFIER | c.967+2827C>A | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 7/10 | chrX | 3092459 | |||||||
chrX:3092622 | A | G | 1 | a0001c0001t0001g0135 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.967+2990A>G | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 7/10 | chrX | 3092622 | |||||||
chrX:3092653 | G | T | 152 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(149): Show |
159 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(156): Show |
intron_variant | MODIFIER | c.967+3021G>T | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 7/10 | chrX | 3092653 | |||||||
chrX:3092835 | T | C | 2 | a0001c0001t0001g0045 a0002c0003t0001g0050 |
2 | HG03225.hp1 HG03654.hp1 |
intron_variant | MODIFIER | c.967+3203T>C | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 7/10 | chrX | 3092835 | |||||||
chrX:3092878 | A | G | 3 | a0004c0006t0001g0008 a0004c0006t0001g0009 a0004c0006t0001g0130 |
3 | HG01168.hp1 HG01169.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.967+3246A>G | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 7/10 | chrX | 3092878 | |||||||
chrX:3092894 | C | T | 1 | a0001c0001t0001g0127 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.967+3262C>T | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 7/10 | chrX | 3092894 | |||||||
chrX:3092901 | G | A | 3 | a0001c0001t0001g0035 a0001c0010t0001g0033 a0001c0010t0001g0040 |
3 | HG02280.hp1 HG02809.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.967+3269G>A | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 7/10 | chrX | 3092901 | |||||||
chrX:3092971 | A | G | 2 | a0001c0001t0001g0141 a0001c0001t0001g0160 |
2 | HG00609.hp1 NA18951.hp2 |
intron_variant | MODIFIER | c.967+3339A>G | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 7/10 | chrX | 3092971 | |||||||
chrX:3093003 | T | C | 1 | a0001c0001t0001g0127 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.967+3371T>C | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 7/10 | chrX | 3093003 | |||||||
chrX:3093012 | T | A | 6 | a0001c0001t0001g0044 a0001c0005t0001g0010 a0001c0005t0001g0012 others(3): Show |
6 | HG01884.hp1 HG01884.hp2 HG02922.hp1 others(3): Show |
intron_variant | MODIFIER | c.967+3380T>A | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 7/10 | chrX | 3093012 | |||||||
chrX:3093020 | C | A | 7 | a0001c0001t0001g0044 a0001c0005t0001g0010 a0001c0005t0001g0012 others(4): Show |
7 | HG01884.hp1 HG01884.hp2 HG02922.hp1 others(4): Show |
intron_variant | MODIFIER | c.967+3388C>A | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 7/10 | chrX | 3093020 | |||||||
chrX:3093022 | C | A | 7 | a0001c0001t0001g0044 a0001c0005t0001g0010 a0001c0005t0001g0012 others(4): Show |
7 | HG01884.hp1 HG01884.hp2 HG02922.hp1 others(4): Show |
intron_variant | MODIFIER | c.967+3390C>A | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 7/10 | chrX | 3093022 | |||||||
chrX:3093023 | A | T | 7 | a0001c0001t0001g0044 a0001c0005t0001g0010 a0001c0005t0001g0012 others(4): Show |
7 | HG01884.hp1 HG01884.hp2 HG02922.hp1 others(4): Show |
intron_variant | MODIFIER | c.967+3391A>T | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 7/10 | chrX | 3093023 | |||||||
chrX:3093024 | T | TAGCTGG | 7 | a0001c0001t0001g0044 a0001c0005t0001g0010 a0001c0005t0001g0012 others(4): Show |
7 | HG01884.hp1 HG01884.hp2 HG02922.hp1 others(4): Show |
intron_variant | MODIFIER | c.967+3392_967+3393i others(8): Show |
ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 7/10 | chrX | 3093024 | |||||||
chrX:3093025 | C | G | 7 | a0001c0001t0001g0044 a0001c0005t0001g0010 a0001c0005t0001g0012 others(4): Show |
7 | HG01884.hp1 HG01884.hp2 HG02922.hp1 others(4): Show |
intron_variant | MODIFIER | c.967+3393C>G | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 7/10 | chrX | 3093025 | |||||||
chrX:3093034 | C | T | 4 | a0001c0001t0001g0038 a0001c0001t0001g0039 a0001c0010t0001g0033 others(1): Show |
4 | HG02280.hp1 HG02451.hp1 HG02809.hp1 others(1): Show |
intron_variant | MODIFIER | c.967+3402C>T | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 7/10 | chrX | 3093034 | |||||||
chrX:3093035 | G | A | 1 | a0004c0006t0001g0130 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.967+3403G>A | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 7/10 | chrX | 3093035 | |||||||
chrX:3093040 | T | C | 59 | a0001c0001t0001g0020 a0001c0001t0001g0038 a0001c0001t0001g0039 others(56): Show |
59 | HG00597.hp1 HG00741.hp2 HG01069.hp1 others(56): Show |
intron_variant | MODIFIER | c.967+3408T>C | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 7/10 | chrX | 3093040 | |||||||
chrX:3093057 | T | C | 10 | a0001c0001t0001g0071 a0001c0002t0001g0015 a0001c0012t0001g0089 others(7): Show |
10 | HG00597.hp1 HG01167.hp1 HG01169.hp1 others(7): Show |
intron_variant | MODIFIER | c.967+3425T>C | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 7/10 | chrX | 3093057 | |||||||
chrX:3093058 | C | T | 10 | a0001c0001t0001g0071 a0001c0002t0001g0015 a0001c0012t0001g0089 others(7): Show |
10 | HG00597.hp1 HG01167.hp1 HG01169.hp1 others(7): Show |
intron_variant | MODIFIER | c.967+3426C>T | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 7/10 | chrX | 3093058 | |||||||
chrX:3093070 | G | T | 4 | a0001c0002t0001g0181 a0001c0002t0001g0183 a0001c0002t0001g0184 others(1): Show |
4 | HG01109.hp1 HG02622.hp2 HG02896.hp2 others(1): Show |
intron_variant | MODIFIER | c.967+3438G>T | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 7/10 | chrX | 3093070 | |||||||
chrX:3093072 | A | G | 1 | a0001c0001t0001g0143 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.967+3440A>G | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 7/10 | chrX | 3093072 | |||||||
chrX:3093090 | T | C | 1 | a0001c0001t0001g0148 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.967+3458T>C | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 7/10 | chrX | 3093090 | |||||||
chrX:3093098 | A | G | 6 | a0001c0001t0001g0068 a0001c0001t0001g0070 a0001c0001t0001g0164 others(3): Show |
6 | HG00735.hp1 HG03041.hp2 HG03225.hp1 others(3): Show |
intron_variant | MODIFIER | c.967+3466A>G | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 7/10 | chrX | 3093098 | |||||||
chrX:3093110 | G | GA | 2 | a0001c0001t0001g0075 a0001c0001t0005g0077 |
2 | NA19056.hp1 NA19083.hp1 |
intron_variant | MODIFIER | c.967+3478_967+3479i others(3): Show |
ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 7/10 | chrX | 3093110 | |||||||
chrX:3093120 | G | C | 1 | a0001c0001t0001g0154 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.967+3488G>C | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 7/10 | chrX | 3093120 | |||||||
chrX:3093144 | A | G | 4 | a0001c0007t0003g0031 a0001c0007t0003g0182 a0002c0003t0001g0050 others(1): Show |
4 | HG02257.hp2 HG02451.hp2 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.967+3512A>G | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 7/10 | chrX | 3093144 | |||||||
chrX:3093147 | G | A | 4 | a0001c0007t0003g0031 a0001c0007t0003g0182 a0002c0003t0001g0050 others(1): Show |
4 | HG02257.hp2 HG02451.hp2 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.967+3515G>A | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 7/10 | chrX | 3093147 | |||||||
chrX:3093151 | C | T | 17 | a0001c0001t0001g0035 a0001c0001t0001g0071 a0001c0002t0001g0015 others(14): Show |
17 | HG00099.hp2 HG00597.hp1 HG01168.hp1 others(14): Show |
intron_variant | MODIFIER | c.967+3519C>T | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 7/10 | chrX | 3093151 | |||||||
chrX:3093152 | G | A | 4 | a0001c0007t0003g0031 a0001c0007t0003g0182 a0002c0003t0001g0050 others(1): Show |
4 | HG02257.hp2 HG02451.hp2 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.967+3520G>A | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 7/10 | chrX | 3093152 | |||||||
chrX:3093159 | C | T | 4 | a0001c0001t0001g0052 a0001c0001t0001g0097 a0001c0001t0001g0125 others(1): Show |
4 | HG02040.hp1 NA18948.hp1 NA18959.hp1 others(1): Show |
intron_variant | MODIFIER | c.967+3527C>T | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 7/10 | chrX | 3093159 | |||||||
chrX:3093160 | G | A | 4 | a0001c0007t0003g0031 a0001c0007t0003g0182 a0002c0003t0001g0050 others(1): Show |
4 | HG02257.hp2 HG02451.hp2 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.967+3528G>A | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 7/10 | chrX | 3093160 | |||||||
chrX:3093292 | G | A | 45 | a0001c0001t0001g0038 a0001c0001t0001g0039 a0001c0001t0001g0051 others(42): Show |
45 | HG00099.hp2 HG00597.hp1 HG01070.hp1 others(42): Show |
intron_variant | MODIFIER | c.967+3660G>A | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 7/10 | chrX | 3093292 | |||||||
chrX:3093313 | GT | G | 2 | a0001c0001t0001g0105 a0001c0001t0001g0178 |
2 | HG02132.hp1 NA19088.hp1 |
intron_variant | MODIFIER | c.967+3682delT | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 7/10 | chrX | 3093313 | |||||||
chrX:3093678 | T | A | 1 | a0001c0012t0001g0089 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.967+4046T>A | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 7/10 | chrX | 3093678 | |||||||
chrX:3093681 | G | A | 4 | a0001c0001t0001g0019 a0001c0001t0001g0091 a0001c0001t0001g0157 others(1): Show |
4 | HG01168.hp2 HG01192.hp1 HG02602.hp1 others(1): Show |
intron_variant | MODIFIER | c.967+4049G>A | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 7/10 | chrX | 3093681 | |||||||
chrX:3093686 | G | C | 9 | a0001c0001t0001g0035 a0001c0015t0006g0021 a0001c0019t0001g0095 others(6): Show |
9 | HG01070.hp1 HG01071.hp2 HG01168.hp1 others(6): Show |
intron_variant | MODIFIER | c.967+4054G>C | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 7/10 | chrX | 3093686 | |||||||
chrX:3093709 | G | A | 5 | a0001c0015t0006g0021 a0001c0019t0001g0095 a0004c0006t0001g0008 others(2): Show |
5 | HG01168.hp1 HG01169.hp2 HG02735.hp1 others(2): Show |
intron_variant | MODIFIER | c.967+4077G>A | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 7/10 | chrX | 3093709 | |||||||
chrX:3093710 | T | G | 26 | a0001c0001t0001g0035 a0001c0002t0001g0022 a0001c0002t0001g0067 others(23): Show |
26 | HG00099.hp2 HG00597.hp1 HG01070.hp1 others(23): Show |
intron_variant | MODIFIER | c.967+4078T>G | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 7/10 | chrX | 3093710 | |||||||
chrX:3093742 | G | A | 2 | a0001c0007t0003g0031 a0001c0007t0003g0182 |
2 | HG02257.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.967+4110G>A | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 7/10 | chrX | 3093742 | |||||||
chrX:3093839 | A | C | 13 | a0001c0002t0001g0022 a0001c0002t0001g0067 a0001c0009t0001g0016 others(10): Show |
13 | HG00099.hp2 HG00597.hp1 HG01167.hp1 others(10): Show |
intron_variant | MODIFIER | c.967+4207A>C | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 7/10 | chrX | 3093839 | |||||||
chrX:3093927 | G | C | 1 | a0001c0001t0001g0171 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.967+4295G>C | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 7/10 | chrX | 3093927 | |||||||
chrX:3094020 | C | G | 4 | a0001c0005t0001g0042 a0001c0005t0001g0043 a0001c0016t0001g0155 others(1): Show |
4 | HG02280.hp2 HG02922.hp1 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.967+4388C>G | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 7/10 | chrX | 3094020 | |||||||
chrX:3094177 | T | C | 11 | a0001c0005t0001g0010 a0001c0005t0001g0012 a0001c0005t0001g0042 others(8): Show |
11 | HG01168.hp1 HG01169.hp2 HG02280.hp2 others(8): Show |
intron_variant | MODIFIER | c.967+4545T>C | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 7/10 | chrX | 3094177 | |||||||
chrX:3094201 | G | C | 4 | a0001c0001t0001g0035 a0002c0004t0001g0090 a0002c0004t0001g0179 others(1): Show |
4 | HG01070.hp1 HG01071.hp2 HG02622.hp1 others(1): Show |
intron_variant | MODIFIER | c.967+4569G>C | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 7/10 | chrX | 3094201 | |||||||
chrX:3094364 | A | G | 26 | a0001c0001t0001g0035 a0001c0002t0001g0022 a0001c0002t0001g0067 others(23): Show |
26 | HG00099.hp2 HG00597.hp1 HG01070.hp1 others(23): Show |
intron_variant | MODIFIER | c.967+4732A>G | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 7/10 | chrX | 3094364 | |||||||
chrX:3094368 | G | A | 2 | a0001c0005t0001g0010 a0001c0005t0001g0012 |
2 | HG03041.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.967+4736G>A | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 7/10 | chrX | 3094368 | |||||||
chrX:3094552 | C | T | 4 | a0001c0007t0003g0031 a0001c0007t0003g0182 a0001c0010t0001g0033 others(1): Show |
4 | HG02257.hp2 HG02280.hp1 HG02809.hp1 others(1): Show |
intron_variant | MODIFIER | c.967+4920C>T | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 7/10 | chrX | 3094552 | |||||||
chrX:3094578 | A | G | 1 | a0001c0001t0001g0039 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.967+4946A>G | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 7/10 | chrX | 3094578 | |||||||
chrX:3094596 | T | C | 4 | a0001c0007t0003g0031 a0001c0007t0003g0182 a0001c0010t0001g0033 others(1): Show |
4 | HG02257.hp2 HG02280.hp1 HG02809.hp1 others(1): Show |
intron_variant | MODIFIER | c.967+4964T>C | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 7/10 | chrX | 3094596 | |||||||
chrX:3094752 | T | C | 4 | a0001c0007t0003g0031 a0001c0007t0003g0182 a0001c0010t0001g0033 others(1): Show |
4 | HG02257.hp2 HG02280.hp1 HG02809.hp1 others(1): Show |
intron_variant | MODIFIER | c.967+5120T>C | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 7/10 | chrX | 3094752 | |||||||
chrX:3094991 | T | G | 13 | a0001c0002t0001g0022 a0001c0002t0001g0067 a0001c0009t0001g0016 others(10): Show |
13 | HG00099.hp2 HG00597.hp1 HG01167.hp1 others(10): Show |
intron_variant | MODIFIER | c.967+5359T>G | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 7/10 | chrX | 3094991 | |||||||
chrX:3095138 | A | C | 11 | a0001c0001t0001g0086 a0001c0002t0001g0022 a0001c0002t0001g0067 others(8): Show |
11 | HG00099.hp2 HG00597.hp1 HG01167.hp1 others(8): Show |
intron_variant | MODIFIER | c.967+5506A>C | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 7/10 | chrX | 3095138 | |||||||
chrX:3095346 | A | G | 29 | a0001c0001t0001g0035 a0001c0001t0001g0086 a0001c0002t0001g0022 others(26): Show |
29 | HG00099.hp2 HG00597.hp1 HG01070.hp1 others(26): Show |
intron_variant | MODIFIER | c.967+5714A>G | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 7/10 | chrX | 3095346 | |||||||
chrX:3095741 | A | G | 2 | a0001c0001t0001g0036 a0001c0001t0001g0037 |
2 | HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.968-5346A>G | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 7/10 | chrX | 3095741 | |||||||
chrX:3095772 | G | A | 14 | a0001c0001t0001g0086 a0001c0002t0001g0022 a0001c0002t0001g0067 others(11): Show |
14 | HG00099.hp2 HG00597.hp1 HG01167.hp1 others(11): Show |
intron_variant | MODIFIER | c.968-5315G>A | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 7/10 | chrX | 3095772 | |||||||
chrX:3095879 | T | A | 4 | a0001c0001t0001g0035 a0002c0004t0001g0090 a0002c0004t0001g0179 others(1): Show |
4 | HG01070.hp1 HG01071.hp2 HG02622.hp1 others(1): Show |
intron_variant | MODIFIER | c.968-5208T>A | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 7/10 | chrX | 3095879 | |||||||
chrX:3095881 | T | C | 43 | a0001c0001t0001g0035 a0001c0001t0001g0051 a0001c0001t0001g0065 others(40): Show |
43 | HG00099.hp2 HG00597.hp1 HG01070.hp1 others(40): Show |
intron_variant | MODIFIER | c.968-5206T>C | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 7/10 | chrX | 3095881 | |||||||
chrX:3095951 | CT | C | 11 | a0001c0005t0001g0010 a0001c0005t0001g0012 a0001c0005t0001g0042 others(8): Show |
11 | HG01168.hp1 HG01169.hp2 HG02280.hp2 others(8): Show |
intron_variant | MODIFIER | c.968-5135delT | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 7/10 | chrX | 3095951 | |||||||
chrX:3096023 | G | A | 17 | a0001c0001t0001g0035 a0001c0002t0001g0022 a0001c0002t0001g0067 others(14): Show |
17 | HG00099.hp2 HG00597.hp1 HG01070.hp1 others(14): Show |
intron_variant | MODIFIER | c.968-5064G>A | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 7/10 | chrX | 3096023 | |||||||
chrX:3096586 | A | G | 1 | a0001c0001t0001g0053 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.968-4501A>G | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 7/10 | chrX | 3096586 | |||||||
chrX:3096816 | TC | T | 13 | a0001c0002t0001g0022 a0001c0002t0001g0067 a0001c0009t0001g0016 others(10): Show |
13 | HG00099.hp2 HG00597.hp1 HG01167.hp1 others(10): Show |
intron_variant | MODIFIER | c.968-4265delC | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chrX | 3096816 | ||||||
chrX:3096977 | G | A | 4 | a0001c0007t0003g0031 a0001c0007t0003g0182 a0001c0010t0001g0033 others(1): Show |
4 | HG02257.hp2 HG02280.hp1 HG02809.hp1 others(1): Show |
intron_variant | MODIFIER | c.968-4110G>A | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 7/10 | chrX | 3096977 | |||||||
chrX:3097481 | A | C | 1 | a0003c0008t0001g0115 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.968-3606A>C | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 7/10 | chrX | 3097481 | |||||||
chrX:3097907 | G | A | 4 | a0001c0007t0003g0031 a0001c0007t0003g0182 a0001c0010t0001g0033 others(1): Show |
4 | HG02257.hp2 HG02280.hp1 HG02809.hp1 others(1): Show |
intron_variant | MODIFIER | c.968-3180G>A | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 7/10 | chrX | 3097907 | |||||||
chrX:3098020 | A | AAT | 15 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0047 others(12): Show |
17 | HG00738.hp1 HG01256.hp1 HG01952.hp1 others(14): Show |
intron_variant | MODIFIER | c.968-3055_968-3054d others(4): Show |
ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chrX | 3098020 | ||||||
chrX:3098020 | A | AATAT | 5 | a0001c0015t0006g0021 a0001c0019t0001g0095 a0004c0006t0001g0008 others(2): Show |
5 | HG01168.hp1 HG01169.hp2 HG02735.hp1 others(2): Show |
intron_variant | MODIFIER | c.968-3057_968-3054d others(6): Show |
ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chrX | 3098020 | ||||||
chrX:3098047 | A | AAC | 14 | a0001c0001t0001g0032 a0001c0001t0001g0051 a0001c0001t0001g0053 others(11): Show |
14 | HG01099.hp1 HG01109.hp1 HG01255.hp1 others(11): Show |
intron_variant | MODIFIER | c.968-3000_968-2999d others(4): Show |
ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chrX | 3098047 | ||||||
chrX:3098047 | A | AACAC | 83 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(80): Show |
89 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(86): Show |
intron_variant | MODIFIER | c.968-3002_968-2999d others(6): Show |
ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chrX | 3098047 | ||||||
chrX:3098047 | A | AACACAC | 29 | a0001c0001t0001g0019 a0001c0001t0001g0045 a0001c0001t0001g0046 others(26): Show |
29 | HG00140.hp1 HG00642.hp1 HG00735.hp1 others(26): Show |
intron_variant | MODIFIER | c.968-3004_968-2999d others(8): Show |
ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chrX | 3098047 | ||||||
chrX:3098047 | A | AACACACA others(1): Show |
20 | a0001c0001t0001g0020 a0001c0001t0001g0101 a0001c0001t0001g0138 others(17): Show |
20 | HG00597.hp2 HG00741.hp2 HG01167.hp1 others(17): Show |
intron_variant | MODIFIER | c.968-3006_968-2999d others(10): Show |
ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chrX | 3098047 | ||||||
chrX:3098047 | A | AACACACA others(3): Show |
7 | a0001c0001t0001g0080 a0001c0001t0001g0125 a0001c0001t0001g0140 others(4): Show |
7 | HG02257.hp1 HG03491.hp1 HG03492.hp1 others(4): Show |
intron_variant | MODIFIER | c.968-3008_968-2999d others(12): Show |
ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chrX | 3098047 | ||||||
chrX:3098047 | A | AACACACA others(5): Show |
1 | a0001c0001t0001g0135 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.968-3010_968-2999d others(14): Show |
ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chrX | 3098047 | ||||||
chrX:3098047 | AAC | A | 2 | a0001c0001t0001g0160 a0002c0003t0001g0050 |
2 | HG00609.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.968-3000_968-2999d others(4): Show |
ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chrX | 3098047 | ||||||
chrX:3098047 | AACAC | A | 11 | a0001c0001t0001g0001 a0001c0001t0001g0039 a0001c0001t0001g0047 others(8): Show |
12 | HG00738.hp1 HG01952.hp1 HG01978.hp2 others(9): Show |
intron_variant | MODIFIER | c.968-3002_968-2999d others(6): Show |
ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chrX | 3098047 | ||||||
chrX:3098047 | AACACAC | A | 5 | a0001c0001t0001g0035 a0001c0001t0001g0048 a0002c0004t0001g0090 others(2): Show |
5 | HG01070.hp1 HG01071.hp2 HG01256.hp1 others(2): Show |
intron_variant | MODIFIER | c.968-3004_968-2999d others(8): Show |
ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chrX | 3098047 | ||||||
chrX:3098131 | A | T | 1 | a0002c0004t0001g0129 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.968-2956A>T | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 7/10 | chrX | 3098131 | |||||||
chrX:3098355 | T | TAG | 13 | a0001c0002t0001g0022 a0001c0002t0001g0067 a0001c0009t0001g0016 others(10): Show |
13 | HG00099.hp2 HG00597.hp1 HG01167.hp1 others(10): Show |
intron_variant | MODIFIER | c.968-2720_968-2719d others(4): Show |
ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chrX | 3098355 | ||||||
chrX:3098523 | G | C | 6 | a0001c0005t0001g0010 a0001c0005t0001g0012 a0001c0005t0001g0042 others(3): Show |
6 | HG02280.hp2 HG02922.hp1 HG03041.hp1 others(3): Show |
intron_variant | MODIFIER | c.968-2564G>C | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 7/10 | chrX | 3098523 | |||||||
chrX:3098610 | G | A | 4 | a0001c0007t0003g0031 a0001c0007t0003g0182 a0001c0010t0001g0033 others(1): Show |
4 | HG02257.hp2 HG02280.hp1 HG02809.hp1 others(1): Show |
intron_variant | MODIFIER | c.968-2477G>A | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 7/10 | chrX | 3098610 | |||||||
chrX:3098657 | G | A | 1 | a0001c0002t0001g0026 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.968-2430G>A | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 7/10 | chrX | 3098657 | |||||||
chrX:3098841 | G | A | 4 | a0001c0001t0001g0035 a0002c0004t0001g0090 a0002c0004t0001g0179 others(1): Show |
4 | HG01070.hp1 HG01071.hp2 HG02622.hp1 others(1): Show |
intron_variant | MODIFIER | c.968-2246G>A | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 7/10 | chrX | 3098841 | |||||||
chrX:3098874 | A | G | 1 | a0001c0001t0001g0142 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.968-2213A>G | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 7/10 | chrX | 3098874 | |||||||
chrX:3099003 | T | C | 1 | a0001c0001t0001g0171 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.968-2084T>C | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 7/10 | chrX | 3099003 | |||||||
chrX:3099014 | G | A | 1 | a0001c0001t0004g0113 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.968-2073G>A | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 7/10 | chrX | 3099014 | |||||||
chrX:3099029 | T | C | 28 | a0001c0001t0001g0035 a0001c0002t0001g0022 a0001c0002t0001g0067 others(25): Show |
28 | HG00099.hp2 HG00597.hp1 HG01070.hp1 others(25): Show |
intron_variant | MODIFIER | c.968-2058T>C | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 7/10 | chrX | 3099029 | |||||||
chrX:3099317 | C | T | 1 | a0001c0002t0001g0067 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.968-1770C>T | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 7/10 | chrX | 3099317 | |||||||
chrX:3099408 | C | T | 4 | a0001c0007t0003g0031 a0001c0007t0003g0182 a0001c0010t0001g0033 others(1): Show |
4 | HG02257.hp2 HG02280.hp1 HG02809.hp1 others(1): Show |
intron_variant | MODIFIER | c.968-1679C>T | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 7/10 | chrX | 3099408 | |||||||
chrX:3099429 | C | A | 1 | a0001c0002t0001g0030 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.968-1658C>A | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 7/10 | chrX | 3099429 | |||||||
chrX:3099476 | A | G | 1 | a0001c0002t0001g0022 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.968-1611A>G | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 7/10 | chrX | 3099476 | |||||||
chrX:3100587 | G | GTTTTTTG others(1): Show |
17 | a0001c0001t0001g0035 a0001c0002t0001g0022 a0001c0002t0001g0067 others(14): Show |
17 | HG00099.hp2 HG00597.hp1 HG01070.hp1 others(14): Show |
intron_variant | MODIFIER | c.968-486_968-479dup others(8): Show |
ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chrX | 3100587 | ||||||
chrX:3100644 | T | C | 45 | a0001c0001t0001g0035 a0001c0001t0001g0038 a0001c0001t0001g0039 others(42): Show |
45 | HG00099.hp2 HG00597.hp1 HG01070.hp1 others(42): Show |
intron_variant | MODIFIER | c.968-443T>C | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 7/10 | chrX | 3100644 | |||||||
chrX:3100690 | C | T | 1 | a0002c0003t0001g0144 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.968-397C>T | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 7/10 | chrX | 3100690 | |||||||
chrX:3100884 | C | G | 17 | a0001c0001t0001g0035 a0001c0002t0001g0022 a0001c0002t0001g0067 others(14): Show |
17 | HG00099.hp2 HG00597.hp1 HG01070.hp1 others(14): Show |
intron_variant | MODIFIER | c.968-203C>G | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 7/10 | chrX | 3100884 | |||||||
chrX:3101073 | G | A | 13 | a0001c0002t0001g0022 a0001c0002t0001g0067 a0001c0009t0001g0016 others(10): Show |
13 | HG00099.hp2 HG00597.hp1 HG01167.hp1 others(10): Show |
intron_variant | MODIFIER | c.968-14G>A | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 7/10 | chrX | 3101073 | |||||||
chrX:3101424 | T | G | 32 | a0001c0001t0001g0035 a0001c0002t0001g0022 a0001c0002t0001g0067 others(29): Show |
32 | HG00099.hp2 HG00597.hp1 HG01070.hp1 others(29): Show |
intron_variant | MODIFIER | c.1102+203T>G | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 8/10 | chrX | 3101424 | |||||||
chrX:3101833 | A | G | 12 | a0001c0002t0001g0022 a0001c0002t0001g0067 a0001c0009t0001g0016 others(9): Show |
12 | HG00099.hp2 HG00597.hp1 HG01167.hp1 others(9): Show |
intron_variant | MODIFIER | c.1102+612A>G | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 8/10 | chrX | 3101833 | |||||||
chrX:3101961 | C | T | 1 | a0001c0001t0001g0160 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.1102+740C>T | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 8/10 | chrX | 3101961 | |||||||
chrX:3102046 | T | C | 1 | a0001c0001t0001g0136 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.1102+825T>C | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 8/10 | chrX | 3102046 | |||||||
chrX:3102135 | T | A | 13 | a0001c0002t0001g0022 a0001c0002t0001g0067 a0001c0009t0001g0016 others(10): Show |
13 | HG00099.hp2 HG00597.hp1 HG01167.hp1 others(10): Show |
intron_variant | MODIFIER | c.1102+914T>A | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 8/10 | chrX | 3102135 | |||||||
chrX:3102195 | T | C | 13 | a0001c0002t0001g0022 a0001c0002t0001g0067 a0001c0009t0001g0016 others(10): Show |
13 | HG00099.hp2 HG00597.hp1 HG01167.hp1 others(10): Show |
intron_variant | MODIFIER | c.1102+974T>C | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 8/10 | chrX | 3102195 | |||||||
chrX:3102257 | T | C | 5 | a0001c0015t0006g0021 a0001c0019t0001g0095 a0004c0006t0001g0008 others(2): Show |
5 | HG01168.hp1 HG01169.hp2 HG02735.hp1 others(2): Show |
intron_variant | MODIFIER | c.1102+1036T>C | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 8/10 | chrX | 3102257 | |||||||
chrX:3102308 | A | G | 17 | a0001c0002t0001g0022 a0001c0002t0001g0067 a0001c0007t0003g0031 others(14): Show |
17 | HG00099.hp2 HG00597.hp1 HG01167.hp1 others(14): Show |
intron_variant | MODIFIER | c.1102+1087A>G | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 8/10 | chrX | 3102308 | |||||||
chrX:3102493 | G | A | 1 | a0001c0001t0001g0035 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1103-1269G>A | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 8/10 | chrX | 3102493 | |||||||
chrX:3102500 | C | T | 1 | a0002c0003t0001g0050 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1103-1262C>T | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 8/10 | chrX | 3102500 | |||||||
chrX:3102594 | C | T | 2 | a0001c0001t0001g0138 a0001c0001t0001g0140 |
2 | HG01517.hp1 HG02257.hp1 |
intron_variant | MODIFIER | c.1103-1168C>T | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 8/10 | chrX | 3102594 | |||||||
chrX:3102617 | G | A | 4 | a0001c0001t0001g0035 a0002c0004t0001g0090 a0002c0004t0001g0179 others(1): Show |
4 | HG01070.hp1 HG01071.hp2 HG02622.hp1 others(1): Show |
intron_variant | MODIFIER | c.1103-1145G>A | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 8/10 | chrX | 3102617 | |||||||
chrX:3102765 | A | G | 1 | a0001c0001t0001g0097 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.1103-997A>G | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 8/10 | chrX | 3102765 | |||||||
chrX:3102799 | C | G | 4 | a0001c0005t0001g0042 a0001c0005t0001g0043 a0001c0016t0001g0155 others(1): Show |
4 | HG02280.hp2 HG02922.hp1 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.1103-963C>G | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 8/10 | chrX | 3102799 | |||||||
chrX:3102809 | G | A | 13 | a0001c0002t0001g0022 a0001c0002t0001g0067 a0001c0009t0001g0016 others(10): Show |
13 | HG00099.hp2 HG00597.hp1 HG01167.hp1 others(10): Show |
intron_variant | MODIFIER | c.1103-953G>A | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 8/10 | chrX | 3102809 | |||||||
chrX:3102826 | G | C | 41 | a0001c0001t0001g0035 a0001c0001t0001g0051 a0001c0001t0001g0065 others(38): Show |
41 | HG00099.hp2 HG00597.hp1 HG01070.hp1 others(38): Show |
intron_variant | MODIFIER | c.1103-936G>C | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 8/10 | chrX | 3102826 | |||||||
chrX:3102827 | G | A | 41 | a0001c0001t0001g0035 a0001c0001t0001g0051 a0001c0001t0001g0065 others(38): Show |
41 | HG00099.hp2 HG00597.hp1 HG01070.hp1 others(38): Show |
intron_variant | MODIFIER | c.1103-935G>A | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 8/10 | chrX | 3102827 | |||||||
chrX:3102829 | G | T | 41 | a0001c0001t0001g0035 a0001c0001t0001g0051 a0001c0001t0001g0065 others(38): Show |
41 | HG00099.hp2 HG00597.hp1 HG01070.hp1 others(38): Show |
intron_variant | MODIFIER | c.1103-933G>T | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 8/10 | chrX | 3102829 | |||||||
chrX:3102860 | C | T | 2 | a0001c0001t0001g0036 a0001c0001t0001g0037 |
2 | HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.1103-902C>T | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 8/10 | chrX | 3102860 | |||||||
chrX:3102862 | C | A | 1 | a0001c0001t0001g0035 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1103-900C>A | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 8/10 | chrX | 3102862 | |||||||
chrX:3102869 | A | G | 7 | a0001c0001t0001g0001 a0001c0001t0001g0047 a0001c0001t0001g0048 others(4): Show |
8 | HG00738.hp1 HG01256.hp1 HG01952.hp1 others(5): Show |
intron_variant | MODIFIER | c.1103-893A>G | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 8/10 | chrX | 3102869 | |||||||
chrX:3102890 | A | G | 1 | a0001c0001t0001g0112 | 1 | NA18988.hp1 | intron_variant | MODIFIER | c.1103-872A>G | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 8/10 | chrX | 3102890 | |||||||
chrX:3102898 | G | C | 1 | a0001c0001t0001g0112 | 1 | NA18988.hp1 | intron_variant | MODIFIER | c.1103-864G>C | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 8/10 | chrX | 3102898 | |||||||
chrX:3102906 | A | G | 4 | a0001c0001t0001g0004 a0001c0001t0001g0123 a0001c0001t0001g0137 others(1): Show |
5 | NA18945.hp1 NA18951.hp2 NA18971.hp1 others(2): Show |
intron_variant | MODIFIER | c.1103-856A>G | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 8/10 | chrX | 3102906 | |||||||
chrX:3102910 | C | CA | 12 | a0001c0001t0001g0035 a0001c0001t0001g0051 a0001c0001t0001g0065 others(9): Show |
12 | HG01070.hp1 HG01071.hp2 HG01109.hp1 others(9): Show |
intron_variant | MODIFIER | c.1103-839dupA | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chrX | 3102910 | ||||||
chrX:3102940 | C | T | 2 | a0001c0010t0001g0033 a0001c0010t0001g0040 |
2 | HG02280.hp1 HG02809.hp1 |
intron_variant | MODIFIER | c.1103-822C>T | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 8/10 | chrX | 3102940 | |||||||
chrX:3103067 | TA | T | 5 | a0001c0015t0006g0021 a0001c0019t0001g0095 a0004c0006t0001g0008 others(2): Show |
5 | HG01168.hp1 HG01169.hp2 HG02735.hp1 others(2): Show |
intron_variant | MODIFIER | c.1103-693delA | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chrX | 3103067 | ||||||
chrX:3103104 | G | C | 1 | a0001c0001t0001g0109 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.1103-658G>C | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 8/10 | chrX | 3103104 | |||||||
chrX:3103194 | C | T | 1 | a0001c0001t0001g0079 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.1103-568C>T | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 8/10 | chrX | 3103194 | |||||||
chrX:3103339 | A | T | 1 | a0002c0004t0001g0129 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.1103-423A>T | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 8/10 | chrX | 3103339 | |||||||
chrX:3103355 | C | T | 1 | a0001c0012t0001g0089 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1103-407C>T | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 8/10 | chrX | 3103355 | |||||||
chrX:3103474 | G | A | 4 | a0001c0001t0001g0035 a0002c0004t0001g0090 a0002c0004t0001g0179 others(1): Show |
4 | HG01070.hp1 HG01071.hp2 HG02622.hp1 others(1): Show |
intron_variant | MODIFIER | c.1103-288G>A | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 8/10 | chrX | 3103474 | |||||||
chrX:3103612 | C | T | 4 | a0001c0001t0001g0035 a0002c0004t0001g0090 a0002c0004t0001g0179 others(1): Show |
4 | HG01070.hp1 HG01071.hp2 HG02622.hp1 others(1): Show |
intron_variant | MODIFIER | c.1103-150C>T | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 8/10 | chrX | 3103612 | |||||||
chrX:3103757 | T | C | 13 | a0001c0002t0001g0022 a0001c0002t0001g0067 a0001c0009t0001g0016 others(10): Show |
13 | HG00099.hp2 HG00597.hp1 HG01167.hp1 others(10): Show |
splice_region_variant&intron_variant | LOW | c.1103-5T>C | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 8/10 | chrX | 3103757 | |||||||
chrX:3104626 | G | A | 1 | a0001c0001t0001g0154 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.1265+702G>A | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 9/10 | chrX | 3104626 | |||||||
chrX:3104677 | G | A | 2 | a0002c0003t0001g0013 a0002c0003t0001g0017 |
2 | HG01167.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.1265+753G>A | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 9/10 | chrX | 3104677 | |||||||
chrX:3104733 | G | C | 1 | a0002c0003t0001g0050 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1265+809G>C | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 9/10 | chrX | 3104733 | |||||||
chrX:3104877 | T | C | 1 | a0001c0001t0001g0039 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.1265+953T>C | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 9/10 | chrX | 3104877 | |||||||
chrX:3105007 | G | A | 1 | a0001c0001t0001g0135 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.1265+1083G>A | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 9/10 | chrX | 3105007 | |||||||
chrX:3105266 | A | G | 17 | a0001c0001t0001g0035 a0001c0002t0001g0022 a0001c0002t0001g0067 others(14): Show |
17 | HG00099.hp2 HG00597.hp1 HG01070.hp1 others(14): Show |
intron_variant | MODIFIER | c.1265+1342A>G | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 9/10 | chrX | 3105266 | |||||||
chrX:3105324 | C | G | 30 | a0001c0001t0001g0035 a0001c0002t0001g0022 a0001c0002t0001g0067 others(27): Show |
30 | HG00099.hp2 HG00597.hp1 HG01070.hp1 others(27): Show |
intron_variant | MODIFIER | c.1265+1400C>G | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 9/10 | chrX | 3105324 | |||||||
chrX:3105429 | C | A | 1 | a0001c0012t0001g0089 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1265+1505C>A | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 9/10 | chrX | 3105429 | |||||||
chrX:3105430 | T | A | 1 | a0001c0012t0001g0089 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1265+1506T>A | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 9/10 | chrX | 3105430 | |||||||
chrX:3105467 | T | C | 2 | a0001c0009t0001g0016 a0001c0009t0001g0018 |
2 | HG03491.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.1265+1543T>C | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 9/10 | chrX | 3105467 | |||||||
chrX:3105496 | G | A | 1 | a0001c0001t0001g0074 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.1265+1572G>A | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 9/10 | chrX | 3105496 | |||||||
chrX:3105600 | G | C | 1 | a0002c0003t0001g0050 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1265+1676G>C | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 9/10 | chrX | 3105600 | |||||||
chrX:3106277 | T | A | 6 | a0001c0005t0001g0010 a0001c0005t0001g0012 a0001c0005t0001g0042 others(3): Show |
6 | HG02280.hp2 HG02922.hp1 HG03041.hp1 others(3): Show |
intron_variant | MODIFIER | c.1265+2353T>A | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 9/10 | chrX | 3106277 | |||||||
chrX:3106281 | G | A | 1 | a0003c0017t0001g0139 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.1265+2357G>A | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 9/10 | chrX | 3106281 | |||||||
chrX:3106324 | A | G | 1 | a0002c0003t0001g0050 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1265+2400A>G | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 9/10 | chrX | 3106324 | |||||||
chrX:3106343 | C | T | 2 | a0001c0007t0003g0031 a0001c0007t0003g0182 |
2 | HG02257.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.1265+2419C>T | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 9/10 | chrX | 3106343 | |||||||
chrX:3106385 | A | T | 3 | a0001c0001t0001g0007 a0001c0001t0001g0064 a0001c0001t0001g0175 |
4 | NA18951.hp1 NA18986.hp1 NA18994.hp1 others(1): Show |
intron_variant | MODIFIER | c.1265+2461A>T | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 9/10 | chrX | 3106385 | |||||||
chrX:3106511 | T | G | 1 | a0001c0001t0001g0051 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.1265+2587T>G | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 9/10 | chrX | 3106511 | |||||||
chrX:3107006 | T | C | 1 | a0005c0022t0001g0169 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.1265+3082T>C | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 9/10 | chrX | 3107006 | |||||||
chrX:3107133 | A | G | 21 | a0001c0001t0001g0035 a0001c0002t0001g0022 a0001c0002t0001g0067 others(18): Show |
21 | HG00099.hp2 HG00597.hp1 HG01070.hp1 others(18): Show |
intron_variant | MODIFIER | c.1266-2995A>G | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 9/10 | chrX | 3107133 | |||||||
chrX:3107368 | C | T | 2 | a0001c0001t0001g0002 a0001c0001t0001g0122 |
3 | HG00735.hp2 HG01070.hp2 HG03490.hp1 |
intron_variant | MODIFIER | c.1266-2760C>T | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 9/10 | chrX | 3107368 | |||||||
chrX:3107433 | G | C | 19 | a0001c0001t0001g0035 a0001c0005t0001g0010 a0001c0005t0001g0012 others(16): Show |
19 | HG01070.hp1 HG01071.hp2 HG01074.hp1 others(16): Show |
intron_variant | MODIFIER | c.1266-2695G>C | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 9/10 | chrX | 3107433 | |||||||
chrX:3107547 | A | G | 19 | a0001c0001t0001g0035 a0001c0005t0001g0010 a0001c0005t0001g0012 others(16): Show |
19 | HG01070.hp1 HG01071.hp2 HG01074.hp1 others(16): Show |
intron_variant | MODIFIER | c.1266-2581A>G | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 9/10 | chrX | 3107547 | |||||||
chrX:3107647 | G | A | 2 | a0001c0007t0003g0031 a0001c0007t0003g0182 |
2 | HG02257.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.1266-2481G>A | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 9/10 | chrX | 3107647 | |||||||
chrX:3107675 | G | C | 4 | a0001c0001t0001g0035 a0002c0004t0001g0090 a0002c0004t0001g0179 others(1): Show |
4 | HG01070.hp1 HG01071.hp2 HG02622.hp1 others(1): Show |
intron_variant | MODIFIER | c.1266-2453G>C | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 9/10 | chrX | 3107675 | |||||||
chrX:3107696 | A | AC | 43 | a0001c0001t0001g0035 a0001c0001t0001g0051 a0001c0001t0001g0065 others(40): Show |
43 | HG00099.hp2 HG00597.hp1 HG01070.hp1 others(40): Show |
intron_variant | MODIFIER | c.1266-2432_1266-243 others(5): Show |
ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 9/10 | chrX | 3107696 | |||||||
chrX:3107732 | C | A | 19 | a0001c0001t0001g0035 a0001c0005t0001g0010 a0001c0005t0001g0012 others(16): Show |
19 | HG01070.hp1 HG01071.hp2 HG01074.hp1 others(16): Show |
intron_variant | MODIFIER | c.1266-2396C>A | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 9/10 | chrX | 3107732 | |||||||
chrX:3107737 | T | C | 19 | a0001c0001t0001g0035 a0001c0005t0001g0010 a0001c0005t0001g0012 others(16): Show |
19 | HG01070.hp1 HG01071.hp2 HG01074.hp1 others(16): Show |
intron_variant | MODIFIER | c.1266-2391T>C | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 9/10 | chrX | 3107737 | |||||||
chrX:3108105 | G | T | 4 | a0003c0008t0001g0115 a0003c0008t0001g0167 a0003c0013t0001g0098 others(1): Show |
4 | HG01074.hp1 HG02258.hp1 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.1266-2023G>T | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 9/10 | chrX | 3108105 | |||||||
chrX:3108697 | T | C | 1 | a0001c0001t0001g0071 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.1266-1431T>C | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 9/10 | chrX | 3108697 | |||||||
chrX:3108945 | G | A | 4 | a0001c0002t0001g0022 a0001c0002t0001g0067 a0001c0009t0001g0016 others(1): Show |
4 | HG03491.hp1 HG03492.hp1 NA19060.hp1 others(1): Show |
intron_variant | MODIFIER | c.1266-1183G>A | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 9/10 | chrX | 3108945 | |||||||
chrX:3109079 | A | G | 15 | a0001c0005t0001g0010 a0001c0005t0001g0012 a0001c0005t0001g0042 others(12): Show |
15 | HG01074.hp1 HG01168.hp1 HG01169.hp2 others(12): Show |
intron_variant | MODIFIER | c.1266-1049A>G | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 9/10 | chrX | 3109079 | |||||||
chrX:3109171 | T | C | 15 | a0001c0005t0001g0010 a0001c0005t0001g0012 a0001c0005t0001g0042 others(12): Show |
15 | HG01074.hp1 HG01168.hp1 HG01169.hp2 others(12): Show |
intron_variant | MODIFIER | c.1266-957T>C | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 9/10 | chrX | 3109171 | |||||||
chrX:3109211 | T | C | 20 | a0001c0001t0001g0038 a0001c0001t0001g0039 a0001c0005t0001g0010 others(17): Show |
20 | HG01070.hp1 HG01071.hp2 HG01074.hp1 others(17): Show |
intron_variant | MODIFIER | c.1266-917T>C | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 9/10 | chrX | 3109211 | |||||||
chrX:3109286 | CT | C | 15 | a0001c0005t0001g0010 a0001c0005t0001g0012 a0001c0005t0001g0042 others(12): Show |
15 | HG01074.hp1 HG01168.hp1 HG01169.hp2 others(12): Show |
intron_variant | MODIFIER | c.1266-841delT | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 9/10 | chrX | 3109286 | |||||||
chrX:3109288 | C | T | 1 | a0002c0003t0001g0144 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.1266-840C>T | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 9/10 | chrX | 3109288 | |||||||
chrX:3109554 | G | A | 4 | a0003c0008t0001g0115 a0003c0008t0001g0167 a0003c0013t0001g0098 others(1): Show |
4 | HG01074.hp1 HG02258.hp1 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.1266-574G>A | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 9/10 | chrX | 3109554 | |||||||
chrX:3109707 | C | T | 1 | a0002c0003t0001g0144 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.1266-421C>T | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 9/10 | chrX | 3109707 | |||||||
chrX:3110013 | G | A | 1 | a0001c0001t0001g0092 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.1266-115G>A | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 9/10 | chrX | 3110013 | |||||||
chrX:3110344 | G | A | 13 | a0001c0005t0001g0042 a0001c0005t0001g0043 a0001c0015t0006g0021 others(10): Show |
13 | HG01074.hp1 HG01168.hp1 HG01169.hp2 others(10): Show |
intron_variant | MODIFIER | c.1390+92G>A | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 10/10 | chrX | 3110344 | |||||||
chrX:3110364 | C | T | 15 | a0001c0005t0001g0010 a0001c0005t0001g0012 a0001c0005t0001g0042 others(12): Show |
15 | HG01074.hp1 HG01168.hp1 HG01169.hp2 others(12): Show |
intron_variant | MODIFIER | c.1390+112C>T | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 10/10 | chrX | 3110364 | |||||||
chrX:3110471 | G | A | 2 | a0001c0001t0001g0125 a0001c0001t0001g0153 |
2 | NA18959.hp1 NA18984.hp1 |
intron_variant | MODIFIER | c.1390+219G>A | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 10/10 | chrX | 3110471 | |||||||
chrX:3110586 | A | G | 15 | a0001c0005t0001g0010 a0001c0005t0001g0012 a0001c0005t0001g0042 others(12): Show |
15 | HG01074.hp1 HG01168.hp1 HG01169.hp2 others(12): Show |
intron_variant | MODIFIER | c.1390+334A>G | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 10/10 | chrX | 3110586 | |||||||
chrX:3111077 | C | T | 35 | a0001c0002t0001g0022 a0001c0002t0001g0067 a0001c0005t0001g0010 others(32): Show |
35 | HG00099.hp2 HG00597.hp1 HG01070.hp1 others(32): Show |
intron_variant | MODIFIER | c.1390+825C>T | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 10/10 | chrX | 3111077 | |||||||
chrX:3111125 | GCTTT | G | 5 | a0001c0015t0006g0021 a0001c0019t0001g0095 a0004c0006t0001g0008 others(2): Show |
5 | HG01168.hp1 HG01169.hp2 HG02735.hp1 others(2): Show |
intron_variant | MODIFIER | c.1390+886_1390+889d others(6): Show |
ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chrX | 3111125 | ||||||
chrX:3111138 | CT | C | 8 | a0001c0001t0001g0081 a0001c0001t0001g0082 a0001c0001t0001g0083 others(5): Show |
8 | HG02071.hp1 NA18612.hp1 NA18952.hp1 others(5): Show |
intron_variant | MODIFIER | c.1390+900delT | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chrX | 3111138 | ||||||
chrX:3111232 | T | G | 1 | a0002c0003t0001g0050 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1391-942T>G | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 10/10 | chrX | 3111232 | |||||||
chrX:3111307 | C | A | 15 | a0001c0005t0001g0010 a0001c0005t0001g0012 a0001c0005t0001g0042 others(12): Show |
15 | HG01074.hp1 HG01168.hp1 HG01169.hp2 others(12): Show |
intron_variant | MODIFIER | c.1391-867C>A | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 10/10 | chrX | 3111307 | |||||||
chrX:3111308 | C | A | 6 | a0002c0003t0001g0013 a0002c0003t0001g0017 a0002c0003t0001g0106 others(3): Show |
6 | HG00099.hp2 HG00597.hp1 HG01167.hp1 others(3): Show |
intron_variant | MODIFIER | c.1391-866C>A | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 10/10 | chrX | 3111308 | |||||||
chrX:3111344 | G | A | 35 | a0001c0002t0001g0022 a0001c0002t0001g0067 a0001c0005t0001g0010 others(32): Show |
35 | HG00099.hp2 HG00597.hp1 HG01070.hp1 others(32): Show |
intron_variant | MODIFIER | c.1391-830G>A | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 10/10 | chrX | 3111344 | |||||||
chrX:3111412 | G | A | 6 | a0001c0005t0001g0010 a0001c0005t0001g0012 a0001c0005t0001g0042 others(3): Show |
6 | HG02280.hp2 HG02922.hp1 HG03041.hp1 others(3): Show |
intron_variant | MODIFIER | c.1391-762G>A | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 10/10 | chrX | 3111412 | |||||||
chrX:3111440 | T | C | 17 | a0001c0002t0001g0022 a0001c0002t0001g0067 a0001c0007t0003g0031 others(14): Show |
17 | HG00099.hp2 HG00597.hp1 HG01167.hp1 others(14): Show |
intron_variant | MODIFIER | c.1391-734T>C | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 10/10 | chrX | 3111440 | |||||||
chrX:3111466 | C | A | 6 | a0001c0005t0001g0010 a0001c0005t0001g0012 a0001c0005t0001g0042 others(3): Show |
6 | HG02280.hp2 HG02922.hp1 HG03041.hp1 others(3): Show |
intron_variant | MODIFIER | c.1391-708C>A | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 10/10 | chrX | 3111466 | |||||||
chrX:3111698 | A | G | 1 | a0006c0018t0002g0131 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.1391-476A>G | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 10/10 | chrX | 3111698 | |||||||
chrX:3111702 | T | C | 15 | a0001c0005t0001g0010 a0001c0005t0001g0012 a0001c0005t0001g0042 others(12): Show |
15 | HG01074.hp1 HG01168.hp1 HG01169.hp2 others(12): Show |
intron_variant | MODIFIER | c.1391-472T>C | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 10/10 | chrX | 3111702 | |||||||
chrX:3111847 | G | A | 1 | a0001c0005t0001g0010 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.1391-327G>A | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 10/10 | chrX | 3111847 | |||||||
chrX:3111964 | C | T | 15 | a0001c0005t0001g0010 a0001c0005t0001g0012 a0001c0005t0001g0042 others(12): Show |
15 | HG01074.hp1 HG01168.hp1 HG01169.hp2 others(12): Show |
intron_variant | MODIFIER | c.1391-210C>T | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 10/10 | chrX | 3111964 | |||||||
chrX:3112140 | G | A | 8 | a0001c0005t0001g0042 a0001c0015t0006g0021 a0001c0016t0001g0155 others(5): Show |
8 | HG01168.hp1 HG01169.hp2 HG02280.hp2 others(5): Show |
intron_variant | MODIFIER | c.1391-34G>A | ARSF | ENSG00000062096.15 | transcript | ENST00000381127.6 | protein_coding | 10/10 | chrX | 3112140 |