Item | Value |
---|---|
geneid | 158521 |
ensemblid | ENSG00000176988.9 |
hgncid | 26372 |
symbol | FMR1NB |
name | FMR1 neighbor |
refseq_nuc | NM_152578.3 |
refseq_prot | NP_689791.1 |
ensembl_nuc | ENST00000370467.8 |
ensembl_prot | ENSP00000359498.3 |
mane_status | MANE Select |
chr | chrX |
start | 147981337 |
end | 148026665 |
strand | + |
ver | v1.2 |
region | chrX:147981337-148026665 |
region5000 | chrX:147976337-148031665 |
regionname0 | FMR1NB_chrX_147981337_148026665 |
regionname5000 | FMR1NB_chrX_147976337_148031665 |
ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 0/1 | 255 | 145 | 27 | 22 | 82 | 3 | 10 | 69 | FMR1NB_chrX_147976337_148031665 | FMR1NB | MSSHR others(250): Show |
chrX | 147976337 | 148031665 |
a0002 | 1/0 | 255 | 130 | 50 | 27 | 26 | 10 | 16 | 12 | FMR1NB_chrX_147976337_148031665 | FMR1NB | MSSHR others(250): Show |
chrX | 147976337 | 148031665 |
achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 0/1 | 765 | 144 | 26 | 22 | 82 | 3 | 10 | FMR1NB_chrX_147976337_148031665 | FMR1NB | ATGTC others(760): Show |
chrX | 147976337 | 148031665 | ||
a0001c0003 | 0/0 | 765 | 1 | 1 | 0 | 0 | 0 | 0 | FMR1NB_chrX_147976337_148031665 | FMR1NB | ATGTC others(760): Show |
chrX | 147976337 | 148031665 | ||
a0002c0002 | 1/0 | 765 | 130 | 50 | 27 | 26 | 10 | 16 | FMR1NB_chrX_147976337_148031665 | FMR1NB | ATGTC others(760): Show |
chrX | 147976337 | 148031665 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 0/1 | 1011 | 143 | 25 | 22 | 82 | 3 | 10 | FMR1NB_chrX_147976337_148031665 | FMR1NB | CTGGG others(1006): Show |
chrX | 147976337 | 148031665 |
a0001c0001t0002 | 0/0 | 1011 | 1 | 1 | 0 | 0 | 0 | 0 | FMR1NB_chrX_147976337_148031665 | FMR1NB | CTGGG others(1006): Show |
chrX | 147976337 | 148031665 |
a0001c0003t0001 | 0/0 | 1011 | 1 | 1 | 0 | 0 | 0 | 0 | FMR1NB_chrX_147976337_148031665 | FMR1NB | CTGGG others(1006): Show |
chrX | 147976337 | 148031665 |
a0002c0002t0001 | 1/0 | 1011 | 130 | 50 | 27 | 26 | 10 | 16 | FMR1NB_chrX_147976337_148031665 | FMR1NB | CTGGG others(1006): Show |
chrX | 147976337 | 148031665 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0001 | 0/0 | 7 | 0 | 1 | 5 | 1 | 0 | FMR1NB_chrX_147976337_148031665 | FMR1NB | chrX | 147976337 | 148031665 |
a0001c0001t0001g0002 | 0/0 | 7 | 0 | 4 | 1 | 1 | 1 | FMR1NB_chrX_147976337_148031665 | FMR1NB | chrX | 147976337 | 148031665 |
a0001c0001t0001g0003 | 0/0 | 6 | 0 | 2 | 4 | 0 | 0 | FMR1NB_chrX_147976337_148031665 | FMR1NB | chrX | 147976337 | 148031665 |
a0001c0001t0001g0004 | 0/0 | 5 | 4 | 1 | 0 | 0 | 0 | FMR1NB_chrX_147976337_148031665 | FMR1NB | chrX | 147976337 | 148031665 |
a0001c0001t0001g0005 | 0/0 | 6 | 0 | 0 | 5 | 0 | 1 | FMR1NB_chrX_147976337_148031665 | FMR1NB | chrX | 147976337 | 148031665 |
a0001c0001t0001g0006 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | FMR1NB_chrX_147976337_148031665 | FMR1NB | chrX | 147976337 | 148031665 |
a0001c0001t0001g0009 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | FMR1NB_chrX_147976337_148031665 | FMR1NB | chrX | 147976337 | 148031665 |
a0001c0001t0001g0010 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | FMR1NB_chrX_147976337_148031665 | FMR1NB | chrX | 147976337 | 148031665 |
a0001c0001t0001g0011 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | FMR1NB_chrX_147976337_148031665 | FMR1NB | chrX | 147976337 | 148031665 |
a0001c0001t0001g0012 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | FMR1NB_chrX_147976337_148031665 | FMR1NB | chrX | 147976337 | 148031665 |
a0001c0001t0001g0018 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FMR1NB_chrX_147976337_148031665 | FMR1NB | chrX | 147976337 | 148031665 |
a0001c0001t0001g0019 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FMR1NB_chrX_147976337_148031665 | FMR1NB | chrX | 147976337 | 148031665 |
a0001c0001t0001g0020 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | FMR1NB_chrX_147976337_148031665 | FMR1NB | chrX | 147976337 | 148031665 |
a0001c0001t0001g0021 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FMR1NB_chrX_147976337_148031665 | FMR1NB | chrX | 147976337 | 148031665 |
a0001c0001t0001g0025 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FMR1NB_chrX_147976337_148031665 | FMR1NB | chrX | 147976337 | 148031665 |
a0001c0001t0001g0026 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | FMR1NB_chrX_147976337_148031665 | FMR1NB | chrX | 147976337 | 148031665 |
a0001c0001t0001g0027 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FMR1NB_chrX_147976337_148031665 | FMR1NB | chrX | 147976337 | 148031665 |
a0001c0001t0001g0028 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | FMR1NB_chrX_147976337_148031665 | FMR1NB | chrX | 147976337 | 148031665 |
a0001c0001t0001g0029 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FMR1NB_chrX_147976337_148031665 | FMR1NB | chrX | 147976337 | 148031665 |
a0001c0001t0001g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FMR1NB_chrX_147976337_148031665 | FMR1NB | chrX | 147976337 | 148031665 |
a0001c0001t0001g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FMR1NB_chrX_147976337_148031665 | FMR1NB | chrX | 147976337 | 148031665 |
a0001c0001t0001g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FMR1NB_chrX_147976337_148031665 | FMR1NB | chrX | 147976337 | 148031665 |
a0001c0001t0001g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FMR1NB_chrX_147976337_148031665 | FMR1NB | chrX | 147976337 | 148031665 |
a0001c0001t0001g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FMR1NB_chrX_147976337_148031665 | FMR1NB | chrX | 147976337 | 148031665 |
a0001c0001t0001g0045 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FMR1NB_chrX_147976337_148031665 | FMR1NB | chrX | 147976337 | 148031665 |
a0001c0001t0001g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FMR1NB_chrX_147976337_148031665 | FMR1NB | chrX | 147976337 | 148031665 |
a0001c0001t0001g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FMR1NB_chrX_147976337_148031665 | FMR1NB | chrX | 147976337 | 148031665 |
a0001c0001t0001g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FMR1NB_chrX_147976337_148031665 | FMR1NB | chrX | 147976337 | 148031665 |
a0001c0001t0001g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FMR1NB_chrX_147976337_148031665 | FMR1NB | chrX | 147976337 | 148031665 |
a0001c0001t0001g0057 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FMR1NB_chrX_147976337_148031665 | FMR1NB | chrX | 147976337 | 148031665 |
a0001c0001t0001g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FMR1NB_chrX_147976337_148031665 | FMR1NB | chrX | 147976337 | 148031665 |
a0001c0001t0001g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FMR1NB_chrX_147976337_148031665 | FMR1NB | chrX | 147976337 | 148031665 |
a0001c0001t0001g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FMR1NB_chrX_147976337_148031665 | FMR1NB | chrX | 147976337 | 148031665 |
a0001c0001t0001g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FMR1NB_chrX_147976337_148031665 | FMR1NB | chrX | 147976337 | 148031665 |
a0001c0001t0001g0062 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FMR1NB_chrX_147976337_148031665 | FMR1NB | chrX | 147976337 | 148031665 |
a0001c0001t0001g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FMR1NB_chrX_147976337_148031665 | FMR1NB | chrX | 147976337 | 148031665 |
a0001c0001t0001g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FMR1NB_chrX_147976337_148031665 | FMR1NB | chrX | 147976337 | 148031665 |
a0001c0001t0001g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FMR1NB_chrX_147976337_148031665 | FMR1NB | chrX | 147976337 | 148031665 |
a0001c0001t0001g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FMR1NB_chrX_147976337_148031665 | FMR1NB | chrX | 147976337 | 148031665 |
a0001c0001t0001g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FMR1NB_chrX_147976337_148031665 | FMR1NB | chrX | 147976337 | 148031665 |
a0001c0001t0001g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FMR1NB_chrX_147976337_148031665 | FMR1NB | chrX | 147976337 | 148031665 |
a0001c0001t0001g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FMR1NB_chrX_147976337_148031665 | FMR1NB | chrX | 147976337 | 148031665 |
a0001c0001t0001g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FMR1NB_chrX_147976337_148031665 | FMR1NB | chrX | 147976337 | 148031665 |
a0001c0001t0001g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FMR1NB_chrX_147976337_148031665 | FMR1NB | chrX | 147976337 | 148031665 |
a0001c0001t0001g0072 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FMR1NB_chrX_147976337_148031665 | FMR1NB | chrX | 147976337 | 148031665 |
a0001c0001t0001g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FMR1NB_chrX_147976337_148031665 | FMR1NB | chrX | 147976337 | 148031665 |
a0001c0001t0001g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FMR1NB_chrX_147976337_148031665 | FMR1NB | chrX | 147976337 | 148031665 |
a0001c0001t0001g0075 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FMR1NB_chrX_147976337_148031665 | FMR1NB | chrX | 147976337 | 148031665 |
a0001c0001t0001g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FMR1NB_chrX_147976337_148031665 | FMR1NB | chrX | 147976337 | 148031665 |
a0001c0001t0001g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FMR1NB_chrX_147976337_148031665 | FMR1NB | chrX | 147976337 | 148031665 |
a0001c0001t0001g0078 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FMR1NB_chrX_147976337_148031665 | FMR1NB | chrX | 147976337 | 148031665 |
a0001c0001t0001g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FMR1NB_chrX_147976337_148031665 | FMR1NB | chrX | 147976337 | 148031665 |
a0001c0001t0001g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FMR1NB_chrX_147976337_148031665 | FMR1NB | chrX | 147976337 | 148031665 |
a0001c0001t0001g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FMR1NB_chrX_147976337_148031665 | FMR1NB | chrX | 147976337 | 148031665 |
a0001c0001t0001g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FMR1NB_chrX_147976337_148031665 | FMR1NB | chrX | 147976337 | 148031665 |
a0001c0001t0001g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FMR1NB_chrX_147976337_148031665 | FMR1NB | chrX | 147976337 | 148031665 |
a0001c0001t0001g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FMR1NB_chrX_147976337_148031665 | FMR1NB | chrX | 147976337 | 148031665 |
a0001c0001t0001g0085 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FMR1NB_chrX_147976337_148031665 | FMR1NB | chrX | 147976337 | 148031665 |
a0001c0001t0001g0086 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FMR1NB_chrX_147976337_148031665 | FMR1NB | chrX | 147976337 | 148031665 |
a0001c0001t0001g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FMR1NB_chrX_147976337_148031665 | FMR1NB | chrX | 147976337 | 148031665 |
a0001c0001t0001g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FMR1NB_chrX_147976337_148031665 | FMR1NB | chrX | 147976337 | 148031665 |
a0001c0001t0001g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FMR1NB_chrX_147976337_148031665 | FMR1NB | chrX | 147976337 | 148031665 |
a0001c0001t0001g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FMR1NB_chrX_147976337_148031665 | FMR1NB | chrX | 147976337 | 148031665 |
a0001c0001t0001g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FMR1NB_chrX_147976337_148031665 | FMR1NB | chrX | 147976337 | 148031665 |
a0001c0001t0001g0092 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FMR1NB_chrX_147976337_148031665 | FMR1NB | chrX | 147976337 | 148031665 |
a0001c0001t0001g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FMR1NB_chrX_147976337_148031665 | FMR1NB | chrX | 147976337 | 148031665 |
a0001c0001t0001g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FMR1NB_chrX_147976337_148031665 | FMR1NB | chrX | 147976337 | 148031665 |
a0001c0001t0001g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FMR1NB_chrX_147976337_148031665 | FMR1NB | chrX | 147976337 | 148031665 |
a0001c0001t0001g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FMR1NB_chrX_147976337_148031665 | FMR1NB | chrX | 147976337 | 148031665 |
a0001c0001t0001g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FMR1NB_chrX_147976337_148031665 | FMR1NB | chrX | 147976337 | 148031665 |
a0001c0001t0001g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FMR1NB_chrX_147976337_148031665 | FMR1NB | chrX | 147976337 | 148031665 |
a0001c0001t0001g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FMR1NB_chrX_147976337_148031665 | FMR1NB | chrX | 147976337 | 148031665 |
a0001c0001t0001g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FMR1NB_chrX_147976337_148031665 | FMR1NB | chrX | 147976337 | 148031665 |
a0001c0001t0001g0128 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FMR1NB_chrX_147976337_148031665 | FMR1NB | chrX | 147976337 | 148031665 |
a0001c0001t0001g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FMR1NB_chrX_147976337_148031665 | FMR1NB | chrX | 147976337 | 148031665 |
a0001c0001t0001g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FMR1NB_chrX_147976337_148031665 | FMR1NB | chrX | 147976337 | 148031665 |
a0001c0001t0001g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FMR1NB_chrX_147976337_148031665 | FMR1NB | chrX | 147976337 | 148031665 |
a0001c0001t0001g0183 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FMR1NB_chrX_147976337_148031665 | FMR1NB | chrX | 147976337 | 148031665 |
a0001c0001t0001g0184 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FMR1NB_chrX_147976337_148031665 | FMR1NB | chrX | 147976337 | 148031665 |
a0001c0001t0001g0185 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FMR1NB_chrX_147976337_148031665 | FMR1NB | chrX | 147976337 | 148031665 |
a0001c0001t0001g0186 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FMR1NB_chrX_147976337_148031665 | FMR1NB | chrX | 147976337 | 148031665 |
a0001c0001t0001g0187 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FMR1NB_chrX_147976337_148031665 | FMR1NB | chrX | 147976337 | 148031665 |
a0001c0001t0001g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FMR1NB_chrX_147976337_148031665 | FMR1NB | chrX | 147976337 | 148031665 |
a0001c0001t0001g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FMR1NB_chrX_147976337_148031665 | FMR1NB | chrX | 147976337 | 148031665 |
a0001c0001t0001g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FMR1NB_chrX_147976337_148031665 | FMR1NB | chrX | 147976337 | 148031665 |
a0001c0001t0001g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FMR1NB_chrX_147976337_148031665 | FMR1NB | chrX | 147976337 | 148031665 |
a0001c0001t0001g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FMR1NB_chrX_147976337_148031665 | FMR1NB | chrX | 147976337 | 148031665 |
a0001c0001t0001g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FMR1NB_chrX_147976337_148031665 | FMR1NB | chrX | 147976337 | 148031665 |
a0001c0001t0001g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FMR1NB_chrX_147976337_148031665 | FMR1NB | chrX | 147976337 | 148031665 |
a0001c0001t0001g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FMR1NB_chrX_147976337_148031665 | FMR1NB | chrX | 147976337 | 148031665 |
a0001c0001t0001g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FMR1NB_chrX_147976337_148031665 | FMR1NB | chrX | 147976337 | 148031665 |
a0001c0001t0001g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FMR1NB_chrX_147976337_148031665 | FMR1NB | chrX | 147976337 | 148031665 |
a0001c0001t0001g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FMR1NB_chrX_147976337_148031665 | FMR1NB | chrX | 147976337 | 148031665 |
a0001c0001t0001g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FMR1NB_chrX_147976337_148031665 | FMR1NB | chrX | 147976337 | 148031665 |
a0001c0001t0001g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FMR1NB_chrX_147976337_148031665 | FMR1NB | chrX | 147976337 | 148031665 |
a0001c0001t0001g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FMR1NB_chrX_147976337_148031665 | FMR1NB | chrX | 147976337 | 148031665 |
a0001c0001t0001g0210 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | FMR1NB_chrX_147976337_148031665 | FMR1NB | chrX | 147976337 | 148031665 |
a0001c0001t0001g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FMR1NB_chrX_147976337_148031665 | FMR1NB | chrX | 147976337 | 148031665 |
a0001c0001t0002g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FMR1NB_chrX_147976337_148031665 | FMR1NB | chrX | 147976337 | 148031665 |
a0001c0003t0001g0004 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FMR1NB_chrX_147976337_148031665 | FMR1NB | chrX | 147976337 | 148031665 |
a0002c0002t0001g0007 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | FMR1NB_chrX_147976337_148031665 | FMR1NB | chrX | 147976337 | 148031665 |
a0002c0002t0001g0008 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | FMR1NB_chrX_147976337_148031665 | FMR1NB | chrX | 147976337 | 148031665 |
a0002c0002t0001g0013 | 0/0 | 3 | 0 | 0 | 1 | 0 | 2 | FMR1NB_chrX_147976337_148031665 | FMR1NB | chrX | 147976337 | 148031665 |
a0002c0002t0001g0014 | 0/0 | 3 | 1 | 0 | 0 | 1 | 1 | FMR1NB_chrX_147976337_148031665 | FMR1NB | chrX | 147976337 | 148031665 |
a0002c0002t0001g0015 | 0/0 | 3 | 0 | 2 | 0 | 1 | 0 | FMR1NB_chrX_147976337_148031665 | FMR1NB | chrX | 147976337 | 148031665 |
a0002c0002t0001g0016 | 0/0 | 3 | 0 | 2 | 1 | 0 | 0 | FMR1NB_chrX_147976337_148031665 | FMR1NB | chrX | 147976337 | 148031665 |
a0002c0002t0001g0017 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FMR1NB_chrX_147976337_148031665 | FMR1NB | chrX | 147976337 | 148031665 |
a0002c0002t0001g0022 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FMR1NB_chrX_147976337_148031665 | FMR1NB | chrX | 147976337 | 148031665 |
a0002c0002t0001g0023 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FMR1NB_chrX_147976337_148031665 | FMR1NB | chrX | 147976337 | 148031665 |
a0002c0002t0001g0024 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FMR1NB_chrX_147976337_148031665 | FMR1NB | chrX | 147976337 | 148031665 |
a0002c0002t0001g0030 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FMR1NB_chrX_147976337_148031665 | FMR1NB | chrX | 147976337 | 148031665 |
a0002c0002t0001g0031 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FMR1NB_chrX_147976337_148031665 | FMR1NB | chrX | 147976337 | 148031665 |
a0002c0002t0001g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FMR1NB_chrX_147976337_148031665 | FMR1NB | chrX | 147976337 | 148031665 |
a0002c0002t0001g0033 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FMR1NB_chrX_147976337_148031665 | FMR1NB | chrX | 147976337 | 148031665 |
a0002c0002t0001g0035 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FMR1NB_chrX_147976337_148031665 | FMR1NB | chrX | 147976337 | 148031665 |
a0002c0002t0001g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FMR1NB_chrX_147976337_148031665 | FMR1NB | chrX | 147976337 | 148031665 |
a0002c0002t0001g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FMR1NB_chrX_147976337_148031665 | FMR1NB | chrX | 147976337 | 148031665 |
a0002c0002t0001g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FMR1NB_chrX_147976337_148031665 | FMR1NB | chrX | 147976337 | 148031665 |
a0002c0002t0001g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FMR1NB_chrX_147976337_148031665 | FMR1NB | chrX | 147976337 | 148031665 |
a0002c0002t0001g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FMR1NB_chrX_147976337_148031665 | FMR1NB | chrX | 147976337 | 148031665 |
a0002c0002t0001g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FMR1NB_chrX_147976337_148031665 | FMR1NB | chrX | 147976337 | 148031665 |
a0002c0002t0001g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FMR1NB_chrX_147976337_148031665 | FMR1NB | chrX | 147976337 | 148031665 |
a0002c0002t0001g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FMR1NB_chrX_147976337_148031665 | FMR1NB | chrX | 147976337 | 148031665 |
a0002c0002t0001g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FMR1NB_chrX_147976337_148031665 | FMR1NB | chrX | 147976337 | 148031665 |
a0002c0002t0001g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FMR1NB_chrX_147976337_148031665 | FMR1NB | chrX | 147976337 | 148031665 |
a0002c0002t0001g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FMR1NB_chrX_147976337_148031665 | FMR1NB | chrX | 147976337 | 148031665 |
a0002c0002t0001g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FMR1NB_chrX_147976337_148031665 | FMR1NB | chrX | 147976337 | 148031665 |
a0002c0002t0001g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FMR1NB_chrX_147976337_148031665 | FMR1NB | chrX | 147976337 | 148031665 |
a0002c0002t0001g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FMR1NB_chrX_147976337_148031665 | FMR1NB | chrX | 147976337 | 148031665 |
a0002c0002t0001g0097 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FMR1NB_chrX_147976337_148031665 | FMR1NB | chrX | 147976337 | 148031665 |
a0002c0002t0001g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FMR1NB_chrX_147976337_148031665 | FMR1NB | chrX | 147976337 | 148031665 |
a0002c0002t0001g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FMR1NB_chrX_147976337_148031665 | FMR1NB | chrX | 147976337 | 148031665 |
a0002c0002t0001g0100 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FMR1NB_chrX_147976337_148031665 | FMR1NB | chrX | 147976337 | 148031665 |
a0002c0002t0001g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FMR1NB_chrX_147976337_148031665 | FMR1NB | chrX | 147976337 | 148031665 |
a0002c0002t0001g0102 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FMR1NB_chrX_147976337_148031665 | FMR1NB | chrX | 147976337 | 148031665 |
a0002c0002t0001g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FMR1NB_chrX_147976337_148031665 | FMR1NB | chrX | 147976337 | 148031665 |
a0002c0002t0001g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FMR1NB_chrX_147976337_148031665 | FMR1NB | chrX | 147976337 | 148031665 |
a0002c0002t0001g0106 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FMR1NB_chrX_147976337_148031665 | FMR1NB | chrX | 147976337 | 148031665 |
a0002c0002t0001g0107 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FMR1NB_chrX_147976337_148031665 | FMR1NB | chrX | 147976337 | 148031665 |
a0002c0002t0001g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FMR1NB_chrX_147976337_148031665 | FMR1NB | chrX | 147976337 | 148031665 |
a0002c0002t0001g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FMR1NB_chrX_147976337_148031665 | FMR1NB | chrX | 147976337 | 148031665 |
a0002c0002t0001g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FMR1NB_chrX_147976337_148031665 | FMR1NB | chrX | 147976337 | 148031665 |
a0002c0002t0001g0114 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FMR1NB_chrX_147976337_148031665 | FMR1NB | chrX | 147976337 | 148031665 |
a0002c0002t0001g0116 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FMR1NB_chrX_147976337_148031665 | FMR1NB | chrX | 147976337 | 148031665 |
a0002c0002t0001g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FMR1NB_chrX_147976337_148031665 | FMR1NB | chrX | 147976337 | 148031665 |
a0002c0002t0001g0118 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FMR1NB_chrX_147976337_148031665 | FMR1NB | chrX | 147976337 | 148031665 |
a0002c0002t0001g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FMR1NB_chrX_147976337_148031665 | FMR1NB | chrX | 147976337 | 148031665 |
a0002c0002t0001g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FMR1NB_chrX_147976337_148031665 | FMR1NB | chrX | 147976337 | 148031665 |
a0002c0002t0001g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FMR1NB_chrX_147976337_148031665 | FMR1NB | chrX | 147976337 | 148031665 |
a0002c0002t0001g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FMR1NB_chrX_147976337_148031665 | FMR1NB | chrX | 147976337 | 148031665 |
a0002c0002t0001g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FMR1NB_chrX_147976337_148031665 | FMR1NB | chrX | 147976337 | 148031665 |
a0002c0002t0001g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FMR1NB_chrX_147976337_148031665 | FMR1NB | chrX | 147976337 | 148031665 |
a0002c0002t0001g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FMR1NB_chrX_147976337_148031665 | FMR1NB | chrX | 147976337 | 148031665 |
a0002c0002t0001g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FMR1NB_chrX_147976337_148031665 | FMR1NB | chrX | 147976337 | 148031665 |
a0002c0002t0001g0129 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FMR1NB_chrX_147976337_148031665 | FMR1NB | chrX | 147976337 | 148031665 |
a0002c0002t0001g0130 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FMR1NB_chrX_147976337_148031665 | FMR1NB | chrX | 147976337 | 148031665 |
a0002c0002t0001g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FMR1NB_chrX_147976337_148031665 | FMR1NB | chrX | 147976337 | 148031665 |
a0002c0002t0001g0132 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FMR1NB_chrX_147976337_148031665 | FMR1NB | chrX | 147976337 | 148031665 |
a0002c0002t0001g0133 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FMR1NB_chrX_147976337_148031665 | FMR1NB | chrX | 147976337 | 148031665 |
a0002c0002t0001g0134 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FMR1NB_chrX_147976337_148031665 | FMR1NB | chrX | 147976337 | 148031665 |
a0002c0002t0001g0135 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FMR1NB_chrX_147976337_148031665 | FMR1NB | chrX | 147976337 | 148031665 |
a0002c0002t0001g0136 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | FMR1NB_chrX_147976337_148031665 | FMR1NB | chrX | 147976337 | 148031665 |
a0002c0002t0001g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FMR1NB_chrX_147976337_148031665 | FMR1NB | chrX | 147976337 | 148031665 |
a0002c0002t0001g0139 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FMR1NB_chrX_147976337_148031665 | FMR1NB | chrX | 147976337 | 148031665 |
a0002c0002t0001g0140 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FMR1NB_chrX_147976337_148031665 | FMR1NB | chrX | 147976337 | 148031665 |
a0002c0002t0001g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FMR1NB_chrX_147976337_148031665 | FMR1NB | chrX | 147976337 | 148031665 |
a0002c0002t0001g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FMR1NB_chrX_147976337_148031665 | FMR1NB | chrX | 147976337 | 148031665 |
a0002c0002t0001g0143 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FMR1NB_chrX_147976337_148031665 | FMR1NB | chrX | 147976337 | 148031665 |
a0002c0002t0001g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FMR1NB_chrX_147976337_148031665 | FMR1NB | chrX | 147976337 | 148031665 |
a0002c0002t0001g0145 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FMR1NB_chrX_147976337_148031665 | FMR1NB | chrX | 147976337 | 148031665 |
a0002c0002t0001g0146 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FMR1NB_chrX_147976337_148031665 | FMR1NB | chrX | 147976337 | 148031665 |
a0002c0002t0001g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FMR1NB_chrX_147976337_148031665 | FMR1NB | chrX | 147976337 | 148031665 |
a0002c0002t0001g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FMR1NB_chrX_147976337_148031665 | FMR1NB | chrX | 147976337 | 148031665 |
a0002c0002t0001g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FMR1NB_chrX_147976337_148031665 | FMR1NB | chrX | 147976337 | 148031665 |
a0002c0002t0001g0150 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FMR1NB_chrX_147976337_148031665 | FMR1NB | chrX | 147976337 | 148031665 |
a0002c0002t0001g0151 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FMR1NB_chrX_147976337_148031665 | FMR1NB | chrX | 147976337 | 148031665 |
a0002c0002t0001g0152 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FMR1NB_chrX_147976337_148031665 | FMR1NB | chrX | 147976337 | 148031665 |
a0002c0002t0001g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FMR1NB_chrX_147976337_148031665 | FMR1NB | chrX | 147976337 | 148031665 |
a0002c0002t0001g0154 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FMR1NB_chrX_147976337_148031665 | FMR1NB | chrX | 147976337 | 148031665 |
a0002c0002t0001g0155 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FMR1NB_chrX_147976337_148031665 | FMR1NB | chrX | 147976337 | 148031665 |
a0002c0002t0001g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FMR1NB_chrX_147976337_148031665 | FMR1NB | chrX | 147976337 | 148031665 |
a0002c0002t0001g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FMR1NB_chrX_147976337_148031665 | FMR1NB | chrX | 147976337 | 148031665 |
a0002c0002t0001g0158 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FMR1NB_chrX_147976337_148031665 | FMR1NB | chrX | 147976337 | 148031665 |
a0002c0002t0001g0159 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FMR1NB_chrX_147976337_148031665 | FMR1NB | chrX | 147976337 | 148031665 |
a0002c0002t0001g0160 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FMR1NB_chrX_147976337_148031665 | FMR1NB | chrX | 147976337 | 148031665 |
a0002c0002t0001g0161 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FMR1NB_chrX_147976337_148031665 | FMR1NB | chrX | 147976337 | 148031665 |
a0002c0002t0001g0162 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FMR1NB_chrX_147976337_148031665 | FMR1NB | chrX | 147976337 | 148031665 |
a0002c0002t0001g0163 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FMR1NB_chrX_147976337_148031665 | FMR1NB | chrX | 147976337 | 148031665 |
a0002c0002t0001g0164 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FMR1NB_chrX_147976337_148031665 | FMR1NB | chrX | 147976337 | 148031665 |
a0002c0002t0001g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FMR1NB_chrX_147976337_148031665 | FMR1NB | chrX | 147976337 | 148031665 |
a0002c0002t0001g0166 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FMR1NB_chrX_147976337_148031665 | FMR1NB | chrX | 147976337 | 148031665 |
a0002c0002t0001g0167 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FMR1NB_chrX_147976337_148031665 | FMR1NB | chrX | 147976337 | 148031665 |
a0002c0002t0001g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FMR1NB_chrX_147976337_148031665 | FMR1NB | chrX | 147976337 | 148031665 |
a0002c0002t0001g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FMR1NB_chrX_147976337_148031665 | FMR1NB | chrX | 147976337 | 148031665 |
a0002c0002t0001g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FMR1NB_chrX_147976337_148031665 | FMR1NB | chrX | 147976337 | 148031665 |
a0002c0002t0001g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FMR1NB_chrX_147976337_148031665 | FMR1NB | chrX | 147976337 | 148031665 |
a0002c0002t0001g0173 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FMR1NB_chrX_147976337_148031665 | FMR1NB | chrX | 147976337 | 148031665 |
a0002c0002t0001g0174 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FMR1NB_chrX_147976337_148031665 | FMR1NB | chrX | 147976337 | 148031665 |
a0002c0002t0001g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FMR1NB_chrX_147976337_148031665 | FMR1NB | chrX | 147976337 | 148031665 |
a0002c0002t0001g0177 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FMR1NB_chrX_147976337_148031665 | FMR1NB | chrX | 147976337 | 148031665 |
a0002c0002t0001g0178 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FMR1NB_chrX_147976337_148031665 | FMR1NB | chrX | 147976337 | 148031665 |
a0002c0002t0001g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FMR1NB_chrX_147976337_148031665 | FMR1NB | chrX | 147976337 | 148031665 |
a0002c0002t0001g0180 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FMR1NB_chrX_147976337_148031665 | FMR1NB | chrX | 147976337 | 148031665 |
a0002c0002t0001g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FMR1NB_chrX_147976337_148031665 | FMR1NB | chrX | 147976337 | 148031665 |
a0002c0002t0001g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FMR1NB_chrX_147976337_148031665 | FMR1NB | chrX | 147976337 | 148031665 |
a0002c0002t0001g0188 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FMR1NB_chrX_147976337_148031665 | FMR1NB | chrX | 147976337 | 148031665 |
a0002c0002t0001g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FMR1NB_chrX_147976337_148031665 | FMR1NB | chrX | 147976337 | 148031665 |
a0002c0002t0001g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FMR1NB_chrX_147976337_148031665 | FMR1NB | chrX | 147976337 | 148031665 |
a0002c0002t0001g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FMR1NB_chrX_147976337_148031665 | FMR1NB | chrX | 147976337 | 148031665 |
a0002c0002t0001g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FMR1NB_chrX_147976337_148031665 | FMR1NB | chrX | 147976337 | 148031665 |
a0002c0002t0001g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FMR1NB_chrX_147976337_148031665 | FMR1NB | chrX | 147976337 | 148031665 |
a0002c0002t0001g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FMR1NB_chrX_147976337_148031665 | FMR1NB | chrX | 147976337 | 148031665 |
a0002c0002t0001g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FMR1NB_chrX_147976337_148031665 | FMR1NB | chrX | 147976337 | 148031665 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0002 | c0002 | t0001 | g0154 | EUR | GBR | FMR1NB_chrX_147976337_148031665 | FMR1NB | chrX | 147976337 | 148031665 |
HG00099 | hp2 | a0002 | c0002 | t0001 | g0132 | EUR | GBR | FMR1NB_chrX_147976337_148031665 | FMR1NB | chrX | 147976337 | 148031665 |
HG00140 | hp1 | a0002 | c0002 | t0001 | g0174 | EUR | GBR | FMR1NB_chrX_147976337_148031665 | FMR1NB | chrX | 147976337 | 148031665 |
HG00280 | hp1 | a0002 | c0002 | t0001 | g0015 | EUR | FIN | FMR1NB_chrX_147976337_148031665 | FMR1NB | chrX | 147976337 | 148031665 |
HG00323 | hp1 | a0001 | c0001 | t0001 | g0001 | EUR | FIN | FMR1NB_chrX_147976337_148031665 | FMR1NB | chrX | 147976337 | 148031665 |
HG00323 | hp2 | a0002 | c0002 | t0001 | g0145 | EUR | FIN | FMR1NB_chrX_147976337_148031665 | FMR1NB | chrX | 147976337 | 148031665 |
HG00408 | hp1 | a0001 | c0001 | t0001 | g0082 | EAS | CHS | FMR1NB_chrX_147976337_148031665 | FMR1NB | chrX | 147976337 | 148031665 |
HG00408 | hp2 | a0002 | c0002 | t0001 | g0153 | EAS | CHS | FMR1NB_chrX_147976337_148031665 | FMR1NB | chrX | 147976337 | 148031665 |
HG00438 | hp1 | a0002 | c0002 | t0001 | g0013 | EAS | CHS | FMR1NB_chrX_147976337_148031665 | FMR1NB | chrX | 147976337 | 148031665 |
HG00438 | hp2 | a0001 | c0001 | t0001 | g0090 | EAS | CHS | FMR1NB_chrX_147976337_148031665 | FMR1NB | chrX | 147976337 | 148031665 |
HG00544 | hp1 | a0001 | c0001 | t0001 | g0055 | EAS | CHS | FMR1NB_chrX_147976337_148031665 | FMR1NB | chrX | 147976337 | 148031665 |
HG00544 | hp2 | a0001 | c0001 | t0001 | g0046 | EAS | CHS | FMR1NB_chrX_147976337_148031665 | FMR1NB | chrX | 147976337 | 148031665 |
HG00597 | hp1 | a0002 | c0002 | t0001 | g0126 | EAS | CHS | FMR1NB_chrX_147976337_148031665 | FMR1NB | chrX | 147976337 | 148031665 |
HG00597 | hp2 | a0001 | c0001 | t0001 | g0021 | EAS | CHS | FMR1NB_chrX_147976337_148031665 | FMR1NB | chrX | 147976337 | 148031665 |
HG00609 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | CHS | FMR1NB_chrX_147976337_148031665 | FMR1NB | chrX | 147976337 | 148031665 |
HG00621 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | FMR1NB_chrX_147976337_148031665 | FMR1NB | chrX | 147976337 | 148031665 |
HG00639 | hp1 | a0001 | c0001 | t0001 | g0004 | AMR | PUR | FMR1NB_chrX_147976337_148031665 | FMR1NB | chrX | 147976337 | 148031665 |
HG00639 | hp2 | a0002 | c0002 | t0001 | g0163 | AMR | PUR | FMR1NB_chrX_147976337_148031665 | FMR1NB | chrX | 147976337 | 148031665 |
HG00642 | hp1 | a0002 | c0002 | t0001 | g0160 | AMR | PUR | FMR1NB_chrX_147976337_148031665 | FMR1NB | chrX | 147976337 | 148031665 |
HG00673 | hp1 | a0002 | c0002 | t0001 | g0007 | EAS | CHS | FMR1NB_chrX_147976337_148031665 | FMR1NB | chrX | 147976337 | 148031665 |
HG00738 | hp1 | a0002 | c0002 | t0001 | g0140 | AMR | PUR | FMR1NB_chrX_147976337_148031665 | FMR1NB | chrX | 147976337 | 148031665 |
HG01069 | hp1 | a0001 | c0001 | t0001 | g0186 | AMR | PUR | FMR1NB_chrX_147976337_148031665 | FMR1NB | chrX | 147976337 | 148031665 |
HG01071 | hp1 | a0002 | c0002 | t0001 | g0173 | AMR | PUR | FMR1NB_chrX_147976337_148031665 | FMR1NB | chrX | 147976337 | 148031665 |
HG01071 | hp2 | a0001 | c0001 | t0001 | g0185 | AMR | PUR | FMR1NB_chrX_147976337_148031665 | FMR1NB | chrX | 147976337 | 148031665 |
HG01074 | hp1 | a0001 | c0001 | t0001 | g0085 | AMR | PUR | FMR1NB_chrX_147976337_148031665 | FMR1NB | chrX | 147976337 | 148031665 |
HG01081 | hp1 | a0002 | c0002 | t0001 | g0152 | AMR | PUR | FMR1NB_chrX_147976337_148031665 | FMR1NB | chrX | 147976337 | 148031665 |
HG01081 | hp2 | a0002 | c0002 | t0001 | g0135 | AMR | PUR | FMR1NB_chrX_147976337_148031665 | FMR1NB | chrX | 147976337 | 148031665 |
HG01099 | hp1 | a0001 | c0001 | t0001 | g0063 | AMR | PUR | FMR1NB_chrX_147976337_148031665 | FMR1NB | chrX | 147976337 | 148031665 |
HG01106 | hp1 | a0002 | c0002 | t0001 | g0150 | AMR | PUR | FMR1NB_chrX_147976337_148031665 | FMR1NB | chrX | 147976337 | 148031665 |
HG01109 | hp1 | a0001 | c0001 | t0001 | g0183 | AMR | PUR | FMR1NB_chrX_147976337_148031665 | FMR1NB | chrX | 147976337 | 148031665 |
HG01168 | hp1 | a0002 | c0002 | t0001 | g0101 | AMR | PUR | FMR1NB_chrX_147976337_148031665 | FMR1NB | chrX | 147976337 | 148031665 |
HG01168 | hp2 | a0001 | c0001 | t0001 | g0028 | AMR | PUR | FMR1NB_chrX_147976337_148031665 | FMR1NB | chrX | 147976337 | 148031665 |
HG01169 | hp1 | a0001 | c0001 | t0001 | g0028 | AMR | PUR | FMR1NB_chrX_147976337_148031665 | FMR1NB | chrX | 147976337 | 148031665 |
HG01169 | hp2 | a0001 | c0001 | t0001 | g0065 | AMR | PUR | FMR1NB_chrX_147976337_148031665 | FMR1NB | chrX | 147976337 | 148031665 |
HG01175 | hp1 | a0002 | c0002 | t0001 | g0159 | AMR | PUR | FMR1NB_chrX_147976337_148031665 | FMR1NB | chrX | 147976337 | 148031665 |
HG01175 | hp2 | a0002 | c0002 | t0001 | g0161 | AMR | PUR | FMR1NB_chrX_147976337_148031665 | FMR1NB | chrX | 147976337 | 148031665 |
HG01192 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | FMR1NB_chrX_147976337_148031665 | FMR1NB | chrX | 147976337 | 148031665 |
HG01243 | hp1 | a0002 | c0002 | t0001 | g0035 | AMR | PUR | FMR1NB_chrX_147976337_148031665 | FMR1NB | chrX | 147976337 | 148031665 |
HG01255 | hp1 | a0002 | c0002 | t0001 | g0143 | AMR | CLM | FMR1NB_chrX_147976337_148031665 | FMR1NB | chrX | 147976337 | 148031665 |
HG01256 | hp1 | a0002 | c0002 | t0001 | g0130 | AMR | CLM | FMR1NB_chrX_147976337_148031665 | FMR1NB | chrX | 147976337 | 148031665 |
HG01258 | hp1 | a0002 | c0002 | t0001 | g0016 | AMR | CLM | FMR1NB_chrX_147976337_148031665 | FMR1NB | chrX | 147976337 | 148031665 |
HG01261 | hp1 | a0001 | c0001 | t0001 | g0086 | AMR | CLM | FMR1NB_chrX_147976337_148031665 | FMR1NB | chrX | 147976337 | 148031665 |
HG01346 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | CLM | FMR1NB_chrX_147976337_148031665 | FMR1NB | chrX | 147976337 | 148031665 |
HG01346 | hp2 | a0002 | c0002 | t0001 | g0151 | AMR | CLM | FMR1NB_chrX_147976337_148031665 | FMR1NB | chrX | 147976337 | 148031665 |
HG01358 | hp1 | a0002 | c0002 | t0001 | g0015 | AMR | CLM | FMR1NB_chrX_147976337_148031665 | FMR1NB | chrX | 147976337 | 148031665 |
HG01361 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | CLM | FMR1NB_chrX_147976337_148031665 | FMR1NB | chrX | 147976337 | 148031665 |
HG01361 | hp2 | a0002 | c0002 | t0001 | g0015 | AMR | CLM | FMR1NB_chrX_147976337_148031665 | FMR1NB | chrX | 147976337 | 148031665 |
HG01433 | hp1 | a0001 | c0001 | t0001 | g0003 | AMR | CLM | FMR1NB_chrX_147976337_148031665 | FMR1NB | chrX | 147976337 | 148031665 |
HG01496 | hp1 | a0002 | c0002 | t0001 | g0129 | AMR | CLM | FMR1NB_chrX_147976337_148031665 | FMR1NB | chrX | 147976337 | 148031665 |
HG01496 | hp2 | a0002 | c0002 | t0001 | g0167 | AMR | CLM | FMR1NB_chrX_147976337_148031665 | FMR1NB | chrX | 147976337 | 148031665 |
HG01515 | hp1 | a0002 | c0002 | t0001 | g0158 | EUR | IBS | FMR1NB_chrX_147976337_148031665 | FMR1NB | chrX | 147976337 | 148031665 |
HG01516 | hp1 | a0001 | c0001 | t0001 | g0002 | EUR | IBS | FMR1NB_chrX_147976337_148031665 | FMR1NB | chrX | 147976337 | 148031665 |
HG01516 | hp2 | a0002 | c0002 | t0001 | g0133 | EUR | IBS | FMR1NB_chrX_147976337_148031665 | FMR1NB | chrX | 147976337 | 148031665 |
HG01517 | hp1 | a0001 | c0001 | t0001 | g0128 | EUR | IBS | FMR1NB_chrX_147976337_148031665 | FMR1NB | chrX | 147976337 | 148031665 |
HG01517 | hp2 | a0002 | c0002 | t0001 | g0014 | EUR | IBS | FMR1NB_chrX_147976337_148031665 | FMR1NB | chrX | 147976337 | 148031665 |
HG01884 | hp1 | a0001 | c0001 | t0001 | g0025 | AFR | ACB | FMR1NB_chrX_147976337_148031665 | FMR1NB | chrX | 147976337 | 148031665 |
HG01884 | hp2 | a0002 | c0002 | t0001 | g0127 | AFR | ACB | FMR1NB_chrX_147976337_148031665 | FMR1NB | chrX | 147976337 | 148031665 |
HG01891 | hp1 | a0001 | c0001 | t0001 | g0095 | AFR | ACB | FMR1NB_chrX_147976337_148031665 | FMR1NB | chrX | 147976337 | 148031665 |
HG01891 | hp2 | a0001 | c0001 | t0001 | g0190 | AFR | ACB | FMR1NB_chrX_147976337_148031665 | FMR1NB | chrX | 147976337 | 148031665 |
HG01928 | hp1 | a0002 | c0002 | t0001 | g0166 | AMR | PEL | FMR1NB_chrX_147976337_148031665 | FMR1NB | chrX | 147976337 | 148031665 |
HG01934 | hp1 | a0002 | c0002 | t0001 | g0033 | AMR | PEL | FMR1NB_chrX_147976337_148031665 | FMR1NB | chrX | 147976337 | 148031665 |
HG01943 | hp1 | a0001 | c0001 | t0001 | g0092 | AMR | PEL | FMR1NB_chrX_147976337_148031665 | FMR1NB | chrX | 147976337 | 148031665 |
HG01952 | hp1 | a0002 | c0002 | t0001 | g0016 | AMR | PEL | FMR1NB_chrX_147976337_148031665 | FMR1NB | chrX | 147976337 | 148031665 |
HG01975 | hp1 | a0002 | c0002 | t0001 | g0180 | AMR | PEL | FMR1NB_chrX_147976337_148031665 | FMR1NB | chrX | 147976337 | 148031665 |
HG01975 | hp2 | a0001 | c0001 | t0001 | g0029 | AMR | PEL | FMR1NB_chrX_147976337_148031665 | FMR1NB | chrX | 147976337 | 148031665 |
HG01978 | hp1 | a0002 | c0002 | t0001 | g0118 | AMR | PEL | FMR1NB_chrX_147976337_148031665 | FMR1NB | chrX | 147976337 | 148031665 |
HG01978 | hp2 | a0002 | c0002 | t0001 | g0114 | AMR | PEL | FMR1NB_chrX_147976337_148031665 | FMR1NB | chrX | 147976337 | 148031665 |
HG02015 | hp1 | a0002 | c0002 | t0001 | g0121 | EAS | KHV | FMR1NB_chrX_147976337_148031665 | FMR1NB | chrX | 147976337 | 148031665 |
HG02027 | hp1 | a0001 | c0001 | t0001 | g0073 | EAS | KHV | FMR1NB_chrX_147976337_148031665 | FMR1NB | chrX | 147976337 | 148031665 |
HG02040 | hp1 | a0002 | c0002 | t0001 | g0007 | EAS | KHV | FMR1NB_chrX_147976337_148031665 | FMR1NB | chrX | 147976337 | 148031665 |
HG02056 | hp1 | a0001 | c0001 | t0001 | g0059 | EAS | KHV | FMR1NB_chrX_147976337_148031665 | FMR1NB | chrX | 147976337 | 148031665 |
HG02071 | hp1 | a0002 | c0002 | t0001 | g0157 | EAS | KHV | FMR1NB_chrX_147976337_148031665 | FMR1NB | chrX | 147976337 | 148031665 |
HG02074 | hp1 | a0001 | c0001 | t0001 | g0088 | EAS | KHV | FMR1NB_chrX_147976337_148031665 | FMR1NB | chrX | 147976337 | 148031665 |
HG02080 | hp1 | a0001 | c0001 | t0001 | g0204 | EAS | KHV | FMR1NB_chrX_147976337_148031665 | FMR1NB | chrX | 147976337 | 148031665 |
HG02080 | hp2 | a0002 | c0002 | t0001 | g0007 | EAS | KHV | FMR1NB_chrX_147976337_148031665 | FMR1NB | chrX | 147976337 | 148031665 |
HG02083 | hp1 | a0001 | c0001 | t0001 | g0009 | EAS | KHV | FMR1NB_chrX_147976337_148031665 | FMR1NB | chrX | 147976337 | 148031665 |
HG02129 | hp1 | a0002 | c0002 | t0001 | g0007 | EAS | KHV | FMR1NB_chrX_147976337_148031665 | FMR1NB | chrX | 147976337 | 148031665 |
HG02132 | hp1 | a0002 | c0002 | t0001 | g0168 | EAS | KHV | FMR1NB_chrX_147976337_148031665 | FMR1NB | chrX | 147976337 | 148031665 |
HG02135 | hp1 | a0002 | c0002 | t0001 | g0189 | EAS | KHV | FMR1NB_chrX_147976337_148031665 | FMR1NB | chrX | 147976337 | 148031665 |
HG02145 | hp1 | a0002 | c0002 | t0001 | g0142 | AFR | ACB | FMR1NB_chrX_147976337_148031665 | FMR1NB | chrX | 147976337 | 148031665 |
HG02148 | hp1 | a0001 | c0001 | t0001 | g0078 | AMR | PEL | FMR1NB_chrX_147976337_148031665 | FMR1NB | chrX | 147976337 | 148031665 |
HG02148 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | PEL | FMR1NB_chrX_147976337_148031665 | FMR1NB | chrX | 147976337 | 148031665 |
HG02257 | hp1 | a0002 | c0002 | t0001 | g0093 | AFR | ACB | FMR1NB_chrX_147976337_148031665 | FMR1NB | chrX | 147976337 | 148031665 |
HG02257 | hp2 | a0001 | c0001 | t0001 | g0192 | AFR | ACB | FMR1NB_chrX_147976337_148031665 | FMR1NB | chrX | 147976337 | 148031665 |
HG02258 | hp1 | a0002 | c0002 | t0001 | g0098 | AFR | ACB | FMR1NB_chrX_147976337_148031665 | FMR1NB | chrX | 147976337 | 148031665 |
HG02273 | hp1 | a0001 | c0001 | t0001 | g0187 | AMR | PEL | FMR1NB_chrX_147976337_148031665 | FMR1NB | chrX | 147976337 | 148031665 |
HG02273 | hp2 | a0002 | c0002 | t0001 | g0031 | AMR | PEL | FMR1NB_chrX_147976337_148031665 | FMR1NB | chrX | 147976337 | 148031665 |
HG02280 | hp1 | a0002 | c0002 | t0001 | g0023 | AFR | ACB | FMR1NB_chrX_147976337_148031665 | FMR1NB | chrX | 147976337 | 148031665 |
HG02280 | hp2 | a0001 | c0001 | t0001 | g0004 | AFR | ACB | FMR1NB_chrX_147976337_148031665 | FMR1NB | chrX | 147976337 | 148031665 |
HG02293 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | PEL | FMR1NB_chrX_147976337_148031665 | FMR1NB | chrX | 147976337 | 148031665 |
HG02293 | hp2 | a0001 | c0001 | t0001 | g0003 | AMR | PEL | FMR1NB_chrX_147976337_148031665 | FMR1NB | chrX | 147976337 | 148031665 |
HG02451 | hp1 | a0002 | c0002 | t0001 | g0099 | AFR | ACB | FMR1NB_chrX_147976337_148031665 | FMR1NB | chrX | 147976337 | 148031665 |
HG02451 | hp2 | a0002 | c0002 | t0001 | g0038 | AFR | ACB | FMR1NB_chrX_147976337_148031665 | FMR1NB | chrX | 147976337 | 148031665 |
HG02523 | hp1 | a0001 | c0001 | t0001 | g0091 | EAS | KHV | FMR1NB_chrX_147976337_148031665 | FMR1NB | chrX | 147976337 | 148031665 |
HG02523 | hp2 | a0002 | c0002 | t0001 | g0117 | EAS | KHV | FMR1NB_chrX_147976337_148031665 | FMR1NB | chrX | 147976337 | 148031665 |
HG02572 | hp1 | a0002 | c0002 | t0001 | g0024 | AFR | GWD | FMR1NB_chrX_147976337_148031665 | FMR1NB | chrX | 147976337 | 148031665 |
HG02602 | hp1 | a0002 | c0002 | t0001 | g0146 | SAS | PJL | FMR1NB_chrX_147976337_148031665 | FMR1NB | chrX | 147976337 | 148031665 |
HG02615 | hp1 | a0002 | c0002 | t0001 | g0008 | AFR | GWD | FMR1NB_chrX_147976337_148031665 | FMR1NB | chrX | 147976337 | 148031665 |
HG02615 | hp2 | a0002 | c0002 | t0001 | g0175 | AFR | GWD | FMR1NB_chrX_147976337_148031665 | FMR1NB | chrX | 147976337 | 148031665 |
HG02622 | hp1 | a0001 | c0001 | t0001 | g0172 | AFR | GWD | FMR1NB_chrX_147976337_148031665 | FMR1NB | chrX | 147976337 | 148031665 |
HG02622 | hp2 | a0002 | c0002 | t0001 | g0103 | AFR | GWD | FMR1NB_chrX_147976337_148031665 | FMR1NB | chrX | 147976337 | 148031665 |
HG02630 | hp1 | a0002 | c0002 | t0001 | g0032 | AFR | GWD | FMR1NB_chrX_147976337_148031665 | FMR1NB | chrX | 147976337 | 148031665 |
HG02630 | hp2 | a0002 | c0002 | t0001 | g0207 | AFR | GWD | FMR1NB_chrX_147976337_148031665 | FMR1NB | chrX | 147976337 | 148031665 |
HG02647 | hp1 | a0002 | c0002 | t0001 | g0037 | AFR | GWD | FMR1NB_chrX_147976337_148031665 | FMR1NB | chrX | 147976337 | 148031665 |
HG02698 | hp1 | a0002 | c0002 | t0001 | g0177 | SAS | PJL | FMR1NB_chrX_147976337_148031665 | FMR1NB | chrX | 147976337 | 148031665 |
HG02717 | hp1 | a0002 | c0002 | t0001 | g0144 | AFR | GWD | FMR1NB_chrX_147976337_148031665 | FMR1NB | chrX | 147976337 | 148031665 |
HG02723 | hp1 | a0002 | c0002 | t0001 | g0113 | AFR | GWD | FMR1NB_chrX_147976337_148031665 | FMR1NB | chrX | 147976337 | 148031665 |
HG02723 | hp2 | a0002 | c0002 | t0001 | g0050 | AFR | GWD | FMR1NB_chrX_147976337_148031665 | FMR1NB | chrX | 147976337 | 148031665 |
HG02735 | hp1 | a0002 | c0002 | t0001 | g0014 | SAS | PJL | FMR1NB_chrX_147976337_148031665 | FMR1NB | chrX | 147976337 | 148031665 |
HG02738 | hp1 | a0001 | c0001 | t0001 | g0184 | SAS | PJL | FMR1NB_chrX_147976337_148031665 | FMR1NB | chrX | 147976337 | 148031665 |
HG02809 | hp1 | a0002 | c0002 | t0001 | g0131 | AFR | GWD | FMR1NB_chrX_147976337_148031665 | FMR1NB | chrX | 147976337 | 148031665 |
HG02809 | hp2 | a0002 | c0002 | t0001 | g0197 | AFR | GWD | FMR1NB_chrX_147976337_148031665 | FMR1NB | chrX | 147976337 | 148031665 |
HG02818 | hp1 | a0002 | c0002 | t0001 | g0040 | AFR | GWD | FMR1NB_chrX_147976337_148031665 | FMR1NB | chrX | 147976337 | 148031665 |
HG02818 | hp2 | a0002 | c0002 | t0001 | g0208 | AFR | GWD | FMR1NB_chrX_147976337_148031665 | FMR1NB | chrX | 147976337 | 148031665 |
HG02886 | hp1 | a0002 | c0002 | t0001 | g0051 | AFR | GWD | FMR1NB_chrX_147976337_148031665 | FMR1NB | chrX | 147976337 | 148031665 |
HG02886 | hp2 | a0002 | c0002 | t0001 | g0119 | AFR | GWD | FMR1NB_chrX_147976337_148031665 | FMR1NB | chrX | 147976337 | 148031665 |
HG02895 | hp1 | a0002 | c0002 | t0001 | g0008 | AFR | GWD | FMR1NB_chrX_147976337_148031665 | FMR1NB | chrX | 147976337 | 148031665 |
HG02896 | hp1 | a0002 | c0002 | t0001 | g0196 | AFR | GWD | FMR1NB_chrX_147976337_148031665 | FMR1NB | chrX | 147976337 | 148031665 |
HG02896 | hp2 | a0002 | c0002 | t0001 | g0104 | AFR | GWD | FMR1NB_chrX_147976337_148031665 | FMR1NB | chrX | 147976337 | 148031665 |
HG02922 | hp1 | a0001 | c0001 | t0001 | g0004 | AFR | ESN | FMR1NB_chrX_147976337_148031665 | FMR1NB | chrX | 147976337 | 148031665 |
HG02922 | hp2 | a0002 | c0002 | t0001 | g0141 | AFR | ESN | FMR1NB_chrX_147976337_148031665 | FMR1NB | chrX | 147976337 | 148031665 |
HG02965 | hp1 | a0002 | c0002 | t0001 | g0111 | AFR | ESN | FMR1NB_chrX_147976337_148031665 | FMR1NB | chrX | 147976337 | 148031665 |
HG02970 | hp1 | a0001 | c0001 | t0001 | g0115 | AFR | ESN | FMR1NB_chrX_147976337_148031665 | FMR1NB | chrX | 147976337 | 148031665 |
HG02970 | hp2 | a0001 | c0001 | t0001 | g0012 | AFR | ESN | FMR1NB_chrX_147976337_148031665 | FMR1NB | chrX | 147976337 | 148031665 |
HG02976 | hp1 | a0002 | c0002 | t0001 | g0212 | AFR | ESN | FMR1NB_chrX_147976337_148031665 | FMR1NB | chrX | 147976337 | 148031665 |
HG02976 | hp2 | a0001 | c0001 | t0001 | g0109 | AFR | ESN | FMR1NB_chrX_147976337_148031665 | FMR1NB | chrX | 147976337 | 148031665 |
HG03017 | hp1 | a0002 | c0002 | t0001 | g0106 | SAS | PJL | FMR1NB_chrX_147976337_148031665 | FMR1NB | chrX | 147976337 | 148031665 |
HG03041 | hp1 | a0002 | c0002 | t0001 | g0052 | AFR | GWD | FMR1NB_chrX_147976337_148031665 | FMR1NB | chrX | 147976337 | 148031665 |
HG03041 | hp2 | a0001 | c0001 | t0001 | g0195 | AFR | GWD | FMR1NB_chrX_147976337_148031665 | FMR1NB | chrX | 147976337 | 148031665 |
HG03098 | hp1 | a0001 | c0001 | t0001 | g0137 | AFR | MSL | FMR1NB_chrX_147976337_148031665 | FMR1NB | chrX | 147976337 | 148031665 |
HG03130 | hp1 | a0001 | c0001 | t0001 | g0108 | AFR | ESN | FMR1NB_chrX_147976337_148031665 | FMR1NB | chrX | 147976337 | 148031665 |
HG03139 | hp1 | a0001 | c0001 | t0001 | g0025 | AFR | ESN | FMR1NB_chrX_147976337_148031665 | FMR1NB | chrX | 147976337 | 148031665 |
HG03195 | hp1 | a0002 | c0002 | t0001 | g0096 | AFR | ESN | FMR1NB_chrX_147976337_148031665 | FMR1NB | chrX | 147976337 | 148031665 |
HG03195 | hp2 | a0002 | c0002 | t0001 | g0206 | AFR | ESN | FMR1NB_chrX_147976337_148031665 | FMR1NB | chrX | 147976337 | 148031665 |
HG03209 | hp1 | a0002 | c0002 | t0001 | g0017 | AFR | MSL | FMR1NB_chrX_147976337_148031665 | FMR1NB | chrX | 147976337 | 148031665 |
HG03225 | hp1 | a0002 | c0002 | t0001 | g0182 | AFR | MSL | FMR1NB_chrX_147976337_148031665 | FMR1NB | chrX | 147976337 | 148031665 |
HG03453 | hp1 | a0002 | c0002 | t0001 | g0039 | AFR | MSL | FMR1NB_chrX_147976337_148031665 | FMR1NB | chrX | 147976337 | 148031665 |
HG03453 | hp2 | a0002 | c0002 | t0001 | g0048 | AFR | MSL | FMR1NB_chrX_147976337_148031665 | FMR1NB | chrX | 147976337 | 148031665 |
HG03486 | hp1 | a0001 | c0001 | t0001 | g0110 | AFR | MSL | FMR1NB_chrX_147976337_148031665 | FMR1NB | chrX | 147976337 | 148031665 |
HG03486 | hp2 | a0002 | c0002 | t0001 | g0017 | AFR | MSL | FMR1NB_chrX_147976337_148031665 | FMR1NB | chrX | 147976337 | 148031665 |
HG03490 | hp1 | a0002 | c0002 | t0001 | g0188 | SAS | PJL | FMR1NB_chrX_147976337_148031665 | FMR1NB | chrX | 147976337 | 148031665 |
HG03491 | hp1 | a0002 | c0002 | t0001 | g0107 | SAS | PJL | FMR1NB_chrX_147976337_148031665 | FMR1NB | chrX | 147976337 | 148031665 |
HG03491 | hp2 | a0001 | c0001 | t0001 | g0020 | SAS | PJL | FMR1NB_chrX_147976337_148031665 | FMR1NB | chrX | 147976337 | 148031665 |
HG03492 | hp1 | a0001 | c0001 | t0001 | g0020 | SAS | PJL | FMR1NB_chrX_147976337_148031665 | FMR1NB | chrX | 147976337 | 148031665 |
HG03516 | hp1 | a0001 | c0001 | t0001 | g0094 | AFR | ESN | FMR1NB_chrX_147976337_148031665 | FMR1NB | chrX | 147976337 | 148031665 |
HG03516 | hp2 | a0002 | c0002 | t0001 | g0148 | AFR | ESN | FMR1NB_chrX_147976337_148031665 | FMR1NB | chrX | 147976337 | 148031665 |
HG03540 | hp1 | a0002 | c0002 | t0001 | g0053 | AFR | GWD | FMR1NB_chrX_147976337_148031665 | FMR1NB | chrX | 147976337 | 148031665 |
HG03540 | hp2 | a0002 | c0002 | t0001 | g0036 | AFR | GWD | FMR1NB_chrX_147976337_148031665 | FMR1NB | chrX | 147976337 | 148031665 |
HG03579 | hp1 | a0001 | c0001 | t0001 | g0201 | AFR | MSL | FMR1NB_chrX_147976337_148031665 | FMR1NB | chrX | 147976337 | 148031665 |
HG03654 | hp1 | a0002 | c0002 | t0001 | g0178 | SAS | PJL | FMR1NB_chrX_147976337_148031665 | FMR1NB | chrX | 147976337 | 148031665 |
HG03669 | hp1 | a0002 | c0002 | t0001 | g0139 | SAS | PJL | FMR1NB_chrX_147976337_148031665 | FMR1NB | chrX | 147976337 | 148031665 |
HG03669 | hp2 | a0002 | c0002 | t0001 | g0102 | SAS | PJL | FMR1NB_chrX_147976337_148031665 | FMR1NB | chrX | 147976337 | 148031665 |
HG03688 | hp1 | a0001 | c0001 | t0001 | g0045 | SAS | STU | FMR1NB_chrX_147976337_148031665 | FMR1NB | chrX | 147976337 | 148031665 |
HG03704 | hp1 | a0002 | c0002 | t0001 | g0013 | SAS | PJL | FMR1NB_chrX_147976337_148031665 | FMR1NB | chrX | 147976337 | 148031665 |
HG03704 | hp2 | a0002 | c0002 | t0001 | g0097 | SAS | PJL | FMR1NB_chrX_147976337_148031665 | FMR1NB | chrX | 147976337 | 148031665 |
HG03710 | hp1 | a0001 | c0001 | t0001 | g0072 | SAS | PJL | FMR1NB_chrX_147976337_148031665 | FMR1NB | chrX | 147976337 | 148031665 |
HG03834 | hp1 | a0002 | c0002 | t0001 | g0100 | SAS | BEB | FMR1NB_chrX_147976337_148031665 | FMR1NB | chrX | 147976337 | 148031665 |
HG03834 | hp2 | a0001 | c0001 | t0001 | g0005 | SAS | BEB | FMR1NB_chrX_147976337_148031665 | FMR1NB | chrX | 147976337 | 148031665 |
HG03942 | hp1 | a0002 | c0002 | t0001 | g0013 | SAS | BEB | FMR1NB_chrX_147976337_148031665 | FMR1NB | chrX | 147976337 | 148031665 |
HG04115 | hp1 | a0002 | c0002 | t0001 | g0030 | SAS | STU | FMR1NB_chrX_147976337_148031665 | FMR1NB | chrX | 147976337 | 148031665 |
HG04184 | hp1 | a0001 | c0001 | t0001 | g0057 | SAS | BEB | FMR1NB_chrX_147976337_148031665 | FMR1NB | chrX | 147976337 | 148031665 |
HG04184 | hp2 | a0001 | c0001 | t0001 | g0062 | SAS | BEB | FMR1NB_chrX_147976337_148031665 | FMR1NB | chrX | 147976337 | 148031665 |
HG04199 | hp1 | a0001 | c0001 | t0001 | g0075 | SAS | STU | FMR1NB_chrX_147976337_148031665 | FMR1NB | chrX | 147976337 | 148031665 |
HG04204 | hp1 | a0002 | c0002 | t0001 | g0162 | SAS | STU | FMR1NB_chrX_147976337_148031665 | FMR1NB | chrX | 147976337 | 148031665 |
HG04228 | hp1 | a0002 | c0002 | t0001 | g0155 | SAS | STU | FMR1NB_chrX_147976337_148031665 | FMR1NB | chrX | 147976337 | 148031665 |
NA18522 | hp1 | a0001 | c0001 | t0001 | g0004 | AFR | YRI | FMR1NB_chrX_147976337_148031665 | FMR1NB | chrX | 147976337 | 148031665 |
NA18612 | hp1 | a0002 | c0002 | t0001 | g0125 | EAS | CHB | FMR1NB_chrX_147976337_148031665 | FMR1NB | chrX | 147976337 | 148031665 |
NA18747 | hp1 | a0002 | c0002 | t0001 | g0054 | EAS | CHB | FMR1NB_chrX_147976337_148031665 | FMR1NB | chrX | 147976337 | 148031665 |
NA18906 | hp1 | a0001 | c0001 | t0001 | g0004 | AFR | YRI | FMR1NB_chrX_147976337_148031665 | FMR1NB | chrX | 147976337 | 148031665 |
NA18906 | hp2 | a0001 | c0001 | t0002 | g0193 | AFR | YRI | FMR1NB_chrX_147976337_148031665 | FMR1NB | chrX | 147976337 | 148031665 |
NA18940 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | FMR1NB_chrX_147976337_148031665 | FMR1NB | chrX | 147976337 | 148031665 |
NA18941 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | FMR1NB_chrX_147976337_148031665 | FMR1NB | chrX | 147976337 | 148031665 |
NA18941 | hp2 | a0001 | c0001 | t0001 | g0205 | EAS | JPT | FMR1NB_chrX_147976337_148031665 | FMR1NB | chrX | 147976337 | 148031665 |
NA18942 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | FMR1NB_chrX_147976337_148031665 | FMR1NB | chrX | 147976337 | 148031665 |
NA18942 | hp2 | a0002 | c0002 | t0001 | g0169 | EAS | JPT | FMR1NB_chrX_147976337_148031665 | FMR1NB | chrX | 147976337 | 148031665 |
NA18943 | hp1 | a0001 | c0001 | t0001 | g0211 | EAS | JPT | FMR1NB_chrX_147976337_148031665 | FMR1NB | chrX | 147976337 | 148031665 |
NA18944 | hp1 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | FMR1NB_chrX_147976337_148031665 | FMR1NB | chrX | 147976337 | 148031665 |
NA18945 | hp1 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | FMR1NB_chrX_147976337_148031665 | FMR1NB | chrX | 147976337 | 148031665 |
NA18947 | hp1 | a0002 | c0002 | t0001 | g0170 | EAS | JPT | FMR1NB_chrX_147976337_148031665 | FMR1NB | chrX | 147976337 | 148031665 |
NA18947 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | FMR1NB_chrX_147976337_148031665 | FMR1NB | chrX | 147976337 | 148031665 |
NA18948 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | FMR1NB_chrX_147976337_148031665 | FMR1NB | chrX | 147976337 | 148031665 |
NA18950 | hp1 | a0001 | c0001 | t0001 | g0066 | EAS | JPT | FMR1NB_chrX_147976337_148031665 | FMR1NB | chrX | 147976337 | 148031665 |
NA18950 | hp2 | a0001 | c0001 | t0001 | g0200 | EAS | JPT | FMR1NB_chrX_147976337_148031665 | FMR1NB | chrX | 147976337 | 148031665 |
NA18952 | hp1 | a0001 | c0001 | t0001 | g0019 | EAS | JPT | FMR1NB_chrX_147976337_148031665 | FMR1NB | chrX | 147976337 | 148031665 |
NA18953 | hp1 | a0001 | c0001 | t0001 | g0089 | EAS | JPT | FMR1NB_chrX_147976337_148031665 | FMR1NB | chrX | 147976337 | 148031665 |
NA18954 | hp1 | a0001 | c0001 | t0001 | g0071 | EAS | JPT | FMR1NB_chrX_147976337_148031665 | FMR1NB | chrX | 147976337 | 148031665 |
NA18954 | hp2 | a0002 | c0002 | t0001 | g0179 | EAS | JPT | FMR1NB_chrX_147976337_148031665 | FMR1NB | chrX | 147976337 | 148031665 |
NA18960 | hp1 | a0001 | c0001 | t0001 | g0064 | EAS | JPT | FMR1NB_chrX_147976337_148031665 | FMR1NB | chrX | 147976337 | 148031665 |
NA18961 | hp1 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | FMR1NB_chrX_147976337_148031665 | FMR1NB | chrX | 147976337 | 148031665 |
NA18962 | hp1 | a0001 | c0001 | t0001 | g0198 | EAS | JPT | FMR1NB_chrX_147976337_148031665 | FMR1NB | chrX | 147976337 | 148031665 |
NA18965 | hp1 | a0001 | c0001 | t0001 | g0044 | EAS | JPT | FMR1NB_chrX_147976337_148031665 | FMR1NB | chrX | 147976337 | 148031665 |
NA18966 | hp1 | a0001 | c0001 | t0001 | g0056 | EAS | JPT | FMR1NB_chrX_147976337_148031665 | FMR1NB | chrX | 147976337 | 148031665 |
NA18967 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | FMR1NB_chrX_147976337_148031665 | FMR1NB | chrX | 147976337 | 148031665 |
NA18970 | hp1 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | FMR1NB_chrX_147976337_148031665 | FMR1NB | chrX | 147976337 | 148031665 |
NA18971 | hp1 | a0001 | c0001 | t0001 | g0042 | EAS | JPT | FMR1NB_chrX_147976337_148031665 | FMR1NB | chrX | 147976337 | 148031665 |
NA18974 | hp1 | a0001 | c0001 | t0001 | g0120 | EAS | JPT | FMR1NB_chrX_147976337_148031665 | FMR1NB | chrX | 147976337 | 148031665 |
NA18977 | hp1 | a0001 | c0001 | t0001 | g0018 | EAS | JPT | FMR1NB_chrX_147976337_148031665 | FMR1NB | chrX | 147976337 | 148031665 |
NA18982 | hp1 | a0001 | c0001 | t0001 | g0087 | EAS | JPT | FMR1NB_chrX_147976337_148031665 | FMR1NB | chrX | 147976337 | 148031665 |
NA18983 | hp1 | a0001 | c0001 | t0001 | g0105 | EAS | JPT | FMR1NB_chrX_147976337_148031665 | FMR1NB | chrX | 147976337 | 148031665 |
NA18984 | hp1 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | FMR1NB_chrX_147976337_148031665 | FMR1NB | chrX | 147976337 | 148031665 |
NA18985 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | FMR1NB_chrX_147976337_148031665 | FMR1NB | chrX | 147976337 | 148031665 |
NA18986 | hp1 | a0001 | c0001 | t0001 | g0070 | EAS | JPT | FMR1NB_chrX_147976337_148031665 | FMR1NB | chrX | 147976337 | 148031665 |
NA18988 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | FMR1NB_chrX_147976337_148031665 | FMR1NB | chrX | 147976337 | 148031665 |
NA18989 | hp1 | a0001 | c0001 | t0001 | g0199 | EAS | JPT | FMR1NB_chrX_147976337_148031665 | FMR1NB | chrX | 147976337 | 148031665 |
NA18990 | hp1 | a0001 | c0001 | t0001 | g0069 | EAS | JPT | FMR1NB_chrX_147976337_148031665 | FMR1NB | chrX | 147976337 | 148031665 |
NA18991 | hp1 | a0002 | c0002 | t0001 | g0022 | EAS | JPT | FMR1NB_chrX_147976337_148031665 | FMR1NB | chrX | 147976337 | 148031665 |
NA18991 | hp2 | a0001 | c0001 | t0001 | g0194 | EAS | JPT | FMR1NB_chrX_147976337_148031665 | FMR1NB | chrX | 147976337 | 148031665 |
NA18992 | hp1 | a0001 | c0001 | t0001 | g0209 | EAS | JPT | FMR1NB_chrX_147976337_148031665 | FMR1NB | chrX | 147976337 | 148031665 |
NA18992 | hp2 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | FMR1NB_chrX_147976337_148031665 | FMR1NB | chrX | 147976337 | 148031665 |
NA18994 | hp1 | a0001 | c0001 | t0001 | g0081 | EAS | JPT | FMR1NB_chrX_147976337_148031665 | FMR1NB | chrX | 147976337 | 148031665 |
NA18995 | hp1 | a0001 | c0001 | t0001 | g0060 | EAS | JPT | FMR1NB_chrX_147976337_148031665 | FMR1NB | chrX | 147976337 | 148031665 |
NA18998 | hp1 | a0001 | c0001 | t0001 | g0067 | EAS | JPT | FMR1NB_chrX_147976337_148031665 | FMR1NB | chrX | 147976337 | 148031665 |
NA18998 | hp2 | a0001 | c0001 | t0001 | g0018 | EAS | JPT | FMR1NB_chrX_147976337_148031665 | FMR1NB | chrX | 147976337 | 148031665 |
NA19000 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | FMR1NB_chrX_147976337_148031665 | FMR1NB | chrX | 147976337 | 148031665 |
NA19002 | hp1 | a0001 | c0001 | t0001 | g0076 | EAS | JPT | FMR1NB_chrX_147976337_148031665 | FMR1NB | chrX | 147976337 | 148031665 |
NA19002 | hp2 | a0001 | c0001 | t0001 | g0068 | EAS | JPT | FMR1NB_chrX_147976337_148031665 | FMR1NB | chrX | 147976337 | 148031665 |
NA19004 | hp1 | a0001 | c0001 | t0001 | g0021 | EAS | JPT | FMR1NB_chrX_147976337_148031665 | FMR1NB | chrX | 147976337 | 148031665 |
NA19005 | hp1 | a0001 | c0001 | t0001 | g0080 | EAS | JPT | FMR1NB_chrX_147976337_148031665 | FMR1NB | chrX | 147976337 | 148031665 |
NA19006 | hp1 | a0001 | c0001 | t0001 | g0027 | EAS | JPT | FMR1NB_chrX_147976337_148031665 | FMR1NB | chrX | 147976337 | 148031665 |
NA19007 | hp1 | a0001 | c0001 | t0001 | g0079 | EAS | JPT | FMR1NB_chrX_147976337_148031665 | FMR1NB | chrX | 147976337 | 148031665 |
NA19009 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | FMR1NB_chrX_147976337_148031665 | FMR1NB | chrX | 147976337 | 148031665 |
NA19012 | hp1 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | FMR1NB_chrX_147976337_148031665 | FMR1NB | chrX | 147976337 | 148031665 |
NA19030 | hp1 | a0002 | c0002 | t0001 | g0049 | AFR | LWK | FMR1NB_chrX_147976337_148031665 | FMR1NB | chrX | 147976337 | 148031665 |
NA19030 | hp2 | a0001 | c0001 | t0001 | g0047 | AFR | LWK | FMR1NB_chrX_147976337_148031665 | FMR1NB | chrX | 147976337 | 148031665 |
NA19043 | hp1 | a0002 | c0002 | t0001 | g0008 | AFR | LWK | FMR1NB_chrX_147976337_148031665 | FMR1NB | chrX | 147976337 | 148031665 |
NA19055 | hp1 | a0001 | c0001 | t0001 | g0083 | EAS | JPT | FMR1NB_chrX_147976337_148031665 | FMR1NB | chrX | 147976337 | 148031665 |
NA19056 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | FMR1NB_chrX_147976337_148031665 | FMR1NB | chrX | 147976337 | 148031665 |
NA19058 | hp1 | a0001 | c0001 | t0001 | g0027 | EAS | JPT | FMR1NB_chrX_147976337_148031665 | FMR1NB | chrX | 147976337 | 148031665 |
NA19060 | hp1 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | FMR1NB_chrX_147976337_148031665 | FMR1NB | chrX | 147976337 | 148031665 |
NA19062 | hp1 | a0002 | c0002 | t0001 | g0165 | EAS | JPT | FMR1NB_chrX_147976337_148031665 | FMR1NB | chrX | 147976337 | 148031665 |
NA19063 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | FMR1NB_chrX_147976337_148031665 | FMR1NB | chrX | 147976337 | 148031665 |
NA19065 | hp1 | a0001 | c0001 | t0001 | g0074 | EAS | JPT | FMR1NB_chrX_147976337_148031665 | FMR1NB | chrX | 147976337 | 148031665 |
NA19065 | hp2 | a0002 | c0002 | t0001 | g0138 | EAS | JPT | FMR1NB_chrX_147976337_148031665 | FMR1NB | chrX | 147976337 | 148031665 |
NA19066 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | FMR1NB_chrX_147976337_148031665 | FMR1NB | chrX | 147976337 | 148031665 |
NA19067 | hp1 | a0001 | c0001 | t0001 | g0061 | EAS | JPT | FMR1NB_chrX_147976337_148031665 | FMR1NB | chrX | 147976337 | 148031665 |
NA19068 | hp1 | a0002 | c0002 | t0001 | g0149 | EAS | JPT | FMR1NB_chrX_147976337_148031665 | FMR1NB | chrX | 147976337 | 148031665 |
NA19070 | hp1 | a0001 | c0001 | t0001 | g0203 | EAS | JPT | FMR1NB_chrX_147976337_148031665 | FMR1NB | chrX | 147976337 | 148031665 |
NA19072 | hp1 | a0001 | c0001 | t0001 | g0043 | EAS | JPT | FMR1NB_chrX_147976337_148031665 | FMR1NB | chrX | 147976337 | 148031665 |
NA19075 | hp1 | a0001 | c0001 | t0001 | g0041 | EAS | JPT | FMR1NB_chrX_147976337_148031665 | FMR1NB | chrX | 147976337 | 148031665 |
NA19076 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | FMR1NB_chrX_147976337_148031665 | FMR1NB | chrX | 147976337 | 148031665 |
NA19079 | hp1 | a0001 | c0001 | t0001 | g0202 | EAS | JPT | FMR1NB_chrX_147976337_148031665 | FMR1NB | chrX | 147976337 | 148031665 |
NA19080 | hp1 | a0001 | c0001 | t0001 | g0084 | EAS | JPT | FMR1NB_chrX_147976337_148031665 | FMR1NB | chrX | 147976337 | 148031665 |
NA19080 | hp2 | a0002 | c0002 | t0001 | g0022 | EAS | JPT | FMR1NB_chrX_147976337_148031665 | FMR1NB | chrX | 147976337 | 148031665 |
NA19081 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | FMR1NB_chrX_147976337_148031665 | FMR1NB | chrX | 147976337 | 148031665 |
NA19081 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | FMR1NB_chrX_147976337_148031665 | FMR1NB | chrX | 147976337 | 148031665 |
NA19082 | hp1 | a0001 | c0001 | t0001 | g0019 | EAS | JPT | FMR1NB_chrX_147976337_148031665 | FMR1NB | chrX | 147976337 | 148031665 |
NA19083 | hp1 | a0001 | c0001 | t0001 | g0058 | EAS | JPT | FMR1NB_chrX_147976337_148031665 | FMR1NB | chrX | 147976337 | 148031665 |
NA19085 | hp1 | a0002 | c0002 | t0001 | g0016 | EAS | JPT | FMR1NB_chrX_147976337_148031665 | FMR1NB | chrX | 147976337 | 148031665 |
NA19086 | hp1 | a0001 | c0001 | t0001 | g0176 | EAS | JPT | FMR1NB_chrX_147976337_148031665 | FMR1NB | chrX | 147976337 | 148031665 |
NA19088 | hp1 | a0002 | c0002 | t0001 | g0122 | EAS | JPT | FMR1NB_chrX_147976337_148031665 | FMR1NB | chrX | 147976337 | 148031665 |
NA19090 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | FMR1NB_chrX_147976337_148031665 | FMR1NB | chrX | 147976337 | 148031665 |
NA19090 | hp2 | a0002 | c0002 | t0001 | g0123 | EAS | JPT | FMR1NB_chrX_147976337_148031665 | FMR1NB | chrX | 147976337 | 148031665 |
NA19091 | hp1 | a0002 | c0002 | t0001 | g0124 | EAS | JPT | FMR1NB_chrX_147976337_148031665 | FMR1NB | chrX | 147976337 | 148031665 |
NA19240 | hp1 | a0001 | c0003 | t0001 | g0004 | AFR | YRI | FMR1NB_chrX_147976337_148031665 | FMR1NB | chrX | 147976337 | 148031665 |
NA19240 | hp2 | a0002 | c0002 | t0001 | g0023 | AFR | YRI | FMR1NB_chrX_147976337_148031665 | FMR1NB | chrX | 147976337 | 148031665 |
NA20129 | hp1 | a0001 | c0001 | t0001 | g0012 | AFR | ASW | FMR1NB_chrX_147976337_148031665 | FMR1NB | chrX | 147976337 | 148031665 |
NA20129 | hp2 | a0002 | c0002 | t0001 | g0112 | AFR | ASW | FMR1NB_chrX_147976337_148031665 | FMR1NB | chrX | 147976337 | 148031665 |
NA20752 | hp1 | a0002 | c0002 | t0001 | g0116 | EUR | TSI | FMR1NB_chrX_147976337_148031665 | FMR1NB | chrX | 147976337 | 148031665 |
NA20805 | hp1 | a0002 | c0002 | t0001 | g0134 | EUR | TSI | FMR1NB_chrX_147976337_148031665 | FMR1NB | chrX | 147976337 | 148031665 |
NA20905 | hp1 | a0001 | c0001 | t0001 | g0002 | SAS | GIH | FMR1NB_chrX_147976337_148031665 | FMR1NB | chrX | 147976337 | 148031665 |
HG01123 | hp1 | a0002 | c0002 | t0001 | g0164 | AMR | CLM | FMR1NB_chrX_147976337_148031665 | FMR1NB | chrX | 147976337 | 148031665 |
HG01123 | hp2 | a0001 | c0001 | t0001 | g0026 | AMR | CLM | FMR1NB_chrX_147976337_148031665 | FMR1NB | chrX | 147976337 | 148031665 |
HG02109 | hp1 | a0002 | c0002 | t0001 | g0171 | AFR | ACB | FMR1NB_chrX_147976337_148031665 | FMR1NB | chrX | 147976337 | 148031665 |
HG02109 | hp2 | a0002 | c0002 | t0001 | g0156 | AFR | ACB | FMR1NB_chrX_147976337_148031665 | FMR1NB | chrX | 147976337 | 148031665 |
HG02486 | hp1 | a0001 | c0001 | t0001 | g0034 | AFR | ACB | FMR1NB_chrX_147976337_148031665 | FMR1NB | chrX | 147976337 | 148031665 |
HG02559 | hp1 | a0002 | c0002 | t0001 | g0014 | AFR | ACB | FMR1NB_chrX_147976337_148031665 | FMR1NB | chrX | 147976337 | 148031665 |
HG02559 | hp2 | a0001 | c0001 | t0001 | g0012 | AFR | ACB | FMR1NB_chrX_147976337_148031665 | FMR1NB | chrX | 147976337 | 148031665 |
HG03471 | hp1 | a0002 | c0002 | t0001 | g0147 | AFR | MSL | FMR1NB_chrX_147976337_148031665 | FMR1NB | chrX | 147976337 | 148031665 |
HG06807 | hp1 | a0001 | c0001 | t0001 | g0191 | AFR | USA | FMR1NB_chrX_147976337_148031665 | FMR1NB | chrX | 147976337 | 148031665 |
HG06807 | hp2 | a0002 | c0002 | t0001 | g0024 | AFR | USA | FMR1NB_chrX_147976337_148031665 | FMR1NB | chrX | 147976337 | 148031665 |
NA18955 | hp1 | a0001 | c0001 | t0001 | g0077 | EAS | JPT | FMR1NB_chrX_147976337_148031665 | FMR1NB | chrX | 147976337 | 148031665 |
NA20300 | hp1 | a0002 | c0002 | t0001 | g0181 | AFR | USA | FMR1NB_chrX_147976337_148031665 | FMR1NB | chrX | 147976337 | 148031665 |
NA20300 | hp2 | a0001 | c0001 | t0001 | g0026 | AFR | USA | FMR1NB_chrX_147976337_148031665 | FMR1NB | chrX | 147976337 | 148031665 |
homoSapiens | chm13v2 | a0001 | c0001 | t0001 | g0210 | REF | REF | FMR1NB_chrX_147976337_148031665 | FMR1NB | chrX | 147976337 | 148031665 |
homoSapiens | grch38p0 | a0002 | c0002 | t0001 | g0136 | REF | REF | FMR1NB_chrX_147976337_148031665 | FMR1NB | chrX | 147976337 | 148031665 |
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:148006729 | C | T | 1 | a0001 | 144 | HG00323.hp1 HG00408.hp1 HG00438.hp2 others(141): Show |
missense_variant | MODERATE | c.425C>T | p.Ala142Val | FMR1NB | ENSG00000176988.9 | transcript | ENST00000370467.8 | protein_coding | 3/6 | 491/1011 | 425/768 | 142/255 | chrX | 148006729 |
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:148008697 | T | C | 1 | a0001c0003 | 1 | NA19240.hp1 | synonymous_variant | LOW | c.618T>C | p.Ser206Ser | FMR1NB | ENSG00000176988.9 | transcript | ENST00000370467.8 | protein_coding | 4/6 | 684/1011 | 618/768 | 206/255 | chrX | 148008697 |
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:147981376 | C | T | 1 | a0001c0001t0002 | 1 | NA18906.hp2 | 5_prime_UTR_variant | MODIFIER | c.-27C>T | FMR1NB | ENSG00000176988.9 | transcript | ENST00000370467.8 | protein_coding | 1/6 | 27 | chrX | 147981376 |
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:147981830 | C | A | 1 | a0001c0001t0001g0029 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.277+151C>A | FMR1NB | ENSG00000176988.9 | transcript | ENST00000370467.8 | protein_coding | 1/5 | chrX | 147981830 | |||||||
chrX:147981908 | G | T | 1 | a0002c0002t0001g0212 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.277+229G>T | FMR1NB | ENSG00000176988.9 | transcript | ENST00000370467.8 | protein_coding | 1/5 | chrX | 147981908 | |||||||
chrX:147982187 | G | A | 1 | a0002c0002t0001g0030 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.277+508G>A | FMR1NB | ENSG00000176988.9 | transcript | ENST00000370467.8 | protein_coding | 1/5 | chrX | 147982187 | |||||||
chrX:147982210 | A | C | 1 | a0001c0001t0001g0211 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.277+531A>C | FMR1NB | ENSG00000176988.9 | transcript | ENST00000370467.8 | protein_coding | 1/5 | chrX | 147982210 | |||||||
chrX:147982245 | G | A | 3 | a0002c0002t0001g0031 a0002c0002t0001g0032 a0002c0002t0001g0033 |
3 | HG01934.hp1 HG02273.hp2 HG02630.hp1 |
intron_variant | MODIFIER | c.277+566G>A | FMR1NB | ENSG00000176988.9 | transcript | ENST00000370467.8 | protein_coding | 1/5 | chrX | 147982245 | |||||||
chrX:147982293 | G | GA | 98 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(95): Show |
131 | HG00323.hp1 HG00408.hp1 HG00438.hp2 others(128): Show |
intron_variant | MODIFIER | c.277+626dupA | FMR1NB | ENSG00000176988.9 | transcript | ENST00000370467.8 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chrX | 147982293 | ||||||
chrX:147982315 | G | A | 1 | a0002c0002t0001g0114 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.277+636G>A | FMR1NB | ENSG00000176988.9 | transcript | ENST00000370467.8 | protein_coding | 1/5 | chrX | 147982315 | |||||||
chrX:147982315 | G | C | 1 | a0001c0001t0001g0034 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.277+636G>C | FMR1NB | ENSG00000176988.9 | transcript | ENST00000370467.8 | protein_coding | 1/5 | chrX | 147982315 | |||||||
chrX:147982455 | G | A | 6 | a0002c0002t0001g0035 a0002c0002t0001g0036 a0002c0002t0001g0037 others(3): Show |
6 | HG01243.hp1 HG02451.hp2 HG02647.hp1 others(3): Show |
intron_variant | MODIFIER | c.277+776G>A | FMR1NB | ENSG00000176988.9 | transcript | ENST00000370467.8 | protein_coding | 1/5 | chrX | 147982455 | |||||||
chrX:147982543 | C | T | 19 | a0001c0001t0001g0005 a0001c0001t0001g0027 a0001c0001t0001g0028 others(16): Show |
26 | HG01168.hp2 HG01169.hp1 HG02080.hp1 others(23): Show |
intron_variant | MODIFIER | c.277+864C>T | FMR1NB | ENSG00000176988.9 | transcript | ENST00000370467.8 | protein_coding | 1/5 | chrX | 147982543 | |||||||
chrX:147982588 | C | CA | 18 | a0001c0001t0001g0041 a0001c0001t0001g0042 a0001c0001t0001g0043 others(15): Show |
21 | HG00544.hp2 HG01243.hp1 HG02615.hp1 others(18): Show |
intron_variant | MODIFIER | c.277+932dupA | FMR1NB | ENSG00000176988.9 | transcript | ENST00000370467.8 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chrX | 147982588 | ||||||
chrX:147982588 | CA | C | 36 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0025 others(33): Show |
50 | HG01069.hp1 HG01071.hp2 HG01109.hp1 others(47): Show |
intron_variant | MODIFIER | c.277+932delA | FMR1NB | ENSG00000176988.9 | transcript | ENST00000370467.8 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chrX | 147982588 | ||||||
chrX:147982606 | A | T | 1 | a0002c0002t0001g0113 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.277+927A>T | FMR1NB | ENSG00000176988.9 | transcript | ENST00000370467.8 | protein_coding | 1/5 | chrX | 147982606 | |||||||
chrX:147982612 | G | T | 4 | a0001c0001t0001g0012 a0001c0001t0001g0108 a0001c0001t0001g0109 others(1): Show |
6 | HG02559.hp2 HG02970.hp2 HG02976.hp2 others(3): Show |
intron_variant | MODIFIER | c.277+933G>T | FMR1NB | ENSG00000176988.9 | transcript | ENST00000370467.8 | protein_coding | 1/5 | chrX | 147982612 | |||||||
chrX:147982627 | G | A | 4 | a0001c0001t0001g0012 a0001c0001t0001g0108 a0001c0001t0001g0109 others(1): Show |
6 | HG02559.hp2 HG02970.hp2 HG02976.hp2 others(3): Show |
intron_variant | MODIFIER | c.277+948G>A | FMR1NB | ENSG00000176988.9 | transcript | ENST00000370467.8 | protein_coding | 1/5 | chrX | 147982627 | |||||||
chrX:147982681 | C | T | 1 | a0002c0002t0001g0178 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.277+1002C>T | FMR1NB | ENSG00000176988.9 | transcript | ENST00000370467.8 | protein_coding | 1/5 | chrX | 147982681 | |||||||
chrX:147982800 | C | T | 4 | a0001c0001t0001g0012 a0001c0001t0001g0108 a0001c0001t0001g0109 others(1): Show |
6 | HG02559.hp2 HG02970.hp2 HG02976.hp2 others(3): Show |
intron_variant | MODIFIER | c.277+1121C>T | FMR1NB | ENSG00000176988.9 | transcript | ENST00000370467.8 | protein_coding | 1/5 | chrX | 147982800 | |||||||
chrX:147982857 | A | G | 99 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(96): Show |
132 | HG00323.hp1 HG00408.hp1 HG00438.hp2 others(129): Show |
intron_variant | MODIFIER | c.277+1178A>G | FMR1NB | ENSG00000176988.9 | transcript | ENST00000370467.8 | protein_coding | 1/5 | chrX | 147982857 | |||||||
chrX:147982872 | C | T | 1 | a0002c0002t0001g0053 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.277+1193C>T | FMR1NB | ENSG00000176988.9 | transcript | ENST00000370467.8 | protein_coding | 1/5 | chrX | 147982872 | |||||||
chrX:147982972 | C | T | 2 | a0002c0002t0001g0106 a0002c0002t0001g0107 |
2 | HG03017.hp1 HG03491.hp1 |
intron_variant | MODIFIER | c.277+1293C>T | FMR1NB | ENSG00000176988.9 | transcript | ENST00000370467.8 | protein_coding | 1/5 | chrX | 147982972 | |||||||
chrX:147983265 | G | A | 97 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(94): Show |
130 | HG00323.hp1 HG00408.hp1 HG00438.hp2 others(127): Show |
intron_variant | MODIFIER | c.277+1586G>A | FMR1NB | ENSG00000176988.9 | transcript | ENST00000370467.8 | protein_coding | 1/5 | chrX | 147983265 | |||||||
chrX:147983704 | G | A | 1 | a0002c0002t0001g0106 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.277+2025G>A | FMR1NB | ENSG00000176988.9 | transcript | ENST00000370467.8 | protein_coding | 1/5 | chrX | 147983704 | |||||||
chrX:147983799 | G | T | 36 | a0001c0001t0001g0004 a0001c0001t0001g0034 a0001c0001t0001g0047 others(33): Show |
43 | HG00639.hp1 HG01168.hp1 HG01243.hp1 others(40): Show |
intron_variant | MODIFIER | c.277+2120G>T | FMR1NB | ENSG00000176988.9 | transcript | ENST00000370467.8 | protein_coding | 1/5 | chrX | 147983799 | |||||||
chrX:147984097 | C | T | 1 | a0001c0001t0002g0193 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.277+2418C>T | FMR1NB | ENSG00000176988.9 | transcript | ENST00000370467.8 | protein_coding | 1/5 | chrX | 147984097 | |||||||
chrX:147984258 | A | G | 1 | a0002c0002t0001g0175 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.277+2579A>G | FMR1NB | ENSG00000176988.9 | transcript | ENST00000370467.8 | protein_coding | 1/5 | chrX | 147984258 | |||||||
chrX:147984420 | G | A | 40 | a0001c0001t0001g0004 a0001c0001t0001g0012 a0001c0001t0001g0034 others(37): Show |
49 | HG00639.hp1 HG01168.hp1 HG01243.hp1 others(46): Show |
intron_variant | MODIFIER | c.277+2741G>A | FMR1NB | ENSG00000176988.9 | transcript | ENST00000370467.8 | protein_coding | 1/5 | chrX | 147984420 | |||||||
chrX:147984595 | C | T | 1 | a0002c0002t0001g0052 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.277+2916C>T | FMR1NB | ENSG00000176988.9 | transcript | ENST00000370467.8 | protein_coding | 1/5 | chrX | 147984595 | |||||||
chrX:147984615 | C | T | 1 | a0002c0002t0001g0112 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.277+2936C>T | FMR1NB | ENSG00000176988.9 | transcript | ENST00000370467.8 | protein_coding | 1/5 | chrX | 147984615 | |||||||
chrX:147984703 | A | C | 40 | a0001c0001t0001g0004 a0001c0001t0001g0012 a0001c0001t0001g0034 others(37): Show |
49 | HG00639.hp1 HG01168.hp1 HG01243.hp1 others(46): Show |
intron_variant | MODIFIER | c.277+3024A>C | FMR1NB | ENSG00000176988.9 | transcript | ENST00000370467.8 | protein_coding | 1/5 | chrX | 147984703 | |||||||
chrX:147985117 | A | G | 2 | a0002c0002t0001g0173 a0002c0002t0001g0174 |
2 | HG00140.hp1 HG01071.hp1 |
intron_variant | MODIFIER | c.277+3438A>G | FMR1NB | ENSG00000176988.9 | transcript | ENST00000370467.8 | protein_coding | 1/5 | chrX | 147985117 | |||||||
chrX:147985448 | C | T | 1 | a0001c0001t0001g0092 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.277+3769C>T | FMR1NB | ENSG00000176988.9 | transcript | ENST00000370467.8 | protein_coding | 1/5 | chrX | 147985448 | |||||||
chrX:147985506 | C | T | 1 | a0001c0001t0001g0091 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.277+3827C>T | FMR1NB | ENSG00000176988.9 | transcript | ENST00000370467.8 | protein_coding | 1/5 | chrX | 147985506 | |||||||
chrX:147985507 | C | T | 5 | a0001c0001t0001g0025 a0001c0001t0001g0026 a0001c0001t0001g0172 others(2): Show |
7 | HG01123.hp2 HG01884.hp1 HG02109.hp1 others(4): Show |
intron_variant | MODIFIER | c.277+3828C>T | FMR1NB | ENSG00000176988.9 | transcript | ENST00000370467.8 | protein_coding | 1/5 | chrX | 147985507 | |||||||
chrX:147985539 | A | G | 58 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0006 others(55): Show |
82 | HG00323.hp1 HG00408.hp1 HG00438.hp2 others(79): Show |
intron_variant | MODIFIER | c.277+3860A>G | FMR1NB | ENSG00000176988.9 | transcript | ENST00000370467.8 | protein_coding | 1/5 | chrX | 147985539 | |||||||
chrX:147985565 | G | A | 1 | a0001c0001t0001g0055 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.277+3886G>A | FMR1NB | ENSG00000176988.9 | transcript | ENST00000370467.8 | protein_coding | 1/5 | chrX | 147985565 | |||||||
chrX:147985700 | T | C | 1 | a0001c0001t0001g0056 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.277+4021T>C | FMR1NB | ENSG00000176988.9 | transcript | ENST00000370467.8 | protein_coding | 1/5 | chrX | 147985700 | |||||||
chrX:147985785 | G | T | 1 | a0002c0002t0001g0017 | 2 | HG03209.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.277+4106G>T | FMR1NB | ENSG00000176988.9 | transcript | ENST00000370467.8 | protein_coding | 1/5 | chrX | 147985785 | |||||||
chrX:147985877 | C | A | 1 | a0002c0002t0001g0117 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.277+4198C>A | FMR1NB | ENSG00000176988.9 | transcript | ENST00000370467.8 | protein_coding | 1/5 | chrX | 147985877 | |||||||
chrX:147985957 | T | G | 1 | a0002c0002t0001g0118 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.277+4278T>G | FMR1NB | ENSG00000176988.9 | transcript | ENST00000370467.8 | protein_coding | 1/5 | chrX | 147985957 | |||||||
chrX:147986113 | G | T | 2 | a0001c0001t0001g0190 a0001c0001t0001g0191 |
2 | HG01891.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.277+4434G>T | FMR1NB | ENSG00000176988.9 | transcript | ENST00000370467.8 | protein_coding | 1/5 | chrX | 147986113 | |||||||
chrX:147986299 | G | A | 1 | a0002c0002t0001g0119 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.277+4620G>A | FMR1NB | ENSG00000176988.9 | transcript | ENST00000370467.8 | protein_coding | 1/5 | chrX | 147986299 | |||||||
chrX:147986318 | G | T | 1 | a0002c0002t0001g0024 | 2 | HG02572.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.277+4639G>T | FMR1NB | ENSG00000176988.9 | transcript | ENST00000370467.8 | protein_coding | 1/5 | chrX | 147986318 | |||||||
chrX:147986386 | C | T | 116 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(113): Show |
156 | HG00323.hp1 HG00408.hp1 HG00438.hp2 others(153): Show |
intron_variant | MODIFIER | c.277+4707C>T | FMR1NB | ENSG00000176988.9 | transcript | ENST00000370467.8 | protein_coding | 1/5 | chrX | 147986386 | |||||||
chrX:147986433 | T | C | 1 | a0001c0001t0001g0105 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.277+4754T>C | FMR1NB | ENSG00000176988.9 | transcript | ENST00000370467.8 | protein_coding | 1/5 | chrX | 147986433 | |||||||
chrX:147986532 | G | A | 9 | a0001c0001t0001g0004 a0001c0001t0001g0047 a0001c0001t0001g0094 others(6): Show |
13 | HG00639.hp1 HG01891.hp1 HG02257.hp1 others(10): Show |
intron_variant | MODIFIER | c.277+4853G>A | FMR1NB | ENSG00000176988.9 | transcript | ENST00000370467.8 | protein_coding | 1/5 | chrX | 147986532 | |||||||
chrX:147986739 | G | A | 1 | a0002c0002t0001g0048 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.277+5060G>A | FMR1NB | ENSG00000176988.9 | transcript | ENST00000370467.8 | protein_coding | 1/5 | chrX | 147986739 | |||||||
chrX:147987013 | G | A | 1 | a0001c0001t0001g0057 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.277+5334G>A | FMR1NB | ENSG00000176988.9 | transcript | ENST00000370467.8 | protein_coding | 1/5 | chrX | 147987013 | |||||||
chrX:147987063 | A | G | 2 | a0002c0002t0001g0169 a0002c0002t0001g0170 |
2 | NA18942.hp2 NA18947.hp1 |
intron_variant | MODIFIER | c.277+5384A>G | FMR1NB | ENSG00000176988.9 | transcript | ENST00000370467.8 | protein_coding | 1/5 | chrX | 147987063 | |||||||
chrX:147987068 | A | G | 1 | a0002c0002t0001g0168 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.277+5389A>G | FMR1NB | ENSG00000176988.9 | transcript | ENST00000370467.8 | protein_coding | 1/5 | chrX | 147987068 | |||||||
chrX:147987383 | G | A | 35 | a0001c0001t0001g0004 a0001c0001t0001g0047 a0001c0001t0001g0094 others(32): Show |
42 | HG00639.hp1 HG01168.hp1 HG01243.hp1 others(39): Show |
intron_variant | MODIFIER | c.277+5704G>A | FMR1NB | ENSG00000176988.9 | transcript | ENST00000370467.8 | protein_coding | 1/5 | chrX | 147987383 | |||||||
chrX:147987665 | G | C | 10 | a0001c0001t0001g0120 a0002c0002t0001g0022 a0002c0002t0001g0121 others(7): Show |
11 | HG00597.hp1 HG01975.hp1 HG02015.hp1 others(8): Show |
intron_variant | MODIFIER | c.277+5986G>C | FMR1NB | ENSG00000176988.9 | transcript | ENST00000370467.8 | protein_coding | 1/5 | chrX | 147987665 | |||||||
chrX:147987711 | A | G | 1 | a0002c0002t0001g0040 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.277+6032A>G | FMR1NB | ENSG00000176988.9 | transcript | ENST00000370467.8 | protein_coding | 1/5 | chrX | 147987711 | |||||||
chrX:147987793 | C | A | 1 | a0002c0002t0001g0197 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.277+6114C>A | FMR1NB | ENSG00000176988.9 | transcript | ENST00000370467.8 | protein_coding | 1/5 | chrX | 147987793 | |||||||
chrX:147987843 | G | GT | 11 | a0001c0001t0001g0021 a0001c0001t0001g0029 a0001c0001t0001g0083 others(8): Show |
12 | HG00438.hp2 HG00597.hp2 HG01074.hp1 others(9): Show |
intron_variant | MODIFIER | c.277+6174dupT | FMR1NB | ENSG00000176988.9 | transcript | ENST00000370467.8 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chrX | 147987843 | ||||||
chrX:147987932 | T | G | 1 | a0002c0002t0001g0053 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.277+6253T>G | FMR1NB | ENSG00000176988.9 | transcript | ENST00000370467.8 | protein_coding | 1/5 | chrX | 147987932 | |||||||
chrX:147988260 | G | A | 5 | a0001c0001t0001g0025 a0001c0001t0001g0026 a0001c0001t0001g0172 others(2): Show |
7 | HG01123.hp2 HG01884.hp1 HG02109.hp1 others(4): Show |
intron_variant | MODIFIER | c.277+6581G>A | FMR1NB | ENSG00000176988.9 | transcript | ENST00000370467.8 | protein_coding | 1/5 | chrX | 147988260 | |||||||
chrX:147988260 | G | T | 40 | a0001c0001t0001g0004 a0001c0001t0001g0012 a0001c0001t0001g0034 others(37): Show |
49 | HG00639.hp1 HG01168.hp1 HG01243.hp1 others(46): Show |
intron_variant | MODIFIER | c.277+6581G>T | FMR1NB | ENSG00000176988.9 | transcript | ENST00000370467.8 | protein_coding | 1/5 | chrX | 147988260 | |||||||
chrX:147988275 | T | C | 1 | a0002c0002t0001g0179 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.277+6596T>C | FMR1NB | ENSG00000176988.9 | transcript | ENST00000370467.8 | protein_coding | 1/5 | chrX | 147988275 | |||||||
chrX:147988334 | G | GC | 40 | a0001c0001t0001g0004 a0001c0001t0001g0012 a0001c0001t0001g0034 others(37): Show |
49 | HG00639.hp1 HG01168.hp1 HG01243.hp1 others(46): Show |
intron_variant | MODIFIER | c.277+6659dupC | FMR1NB | ENSG00000176988.9 | transcript | ENST00000370467.8 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chrX | 147988334 | ||||||
chrX:147988595 | T | C | 2 | a0001c0001t0001g0198 a0001c0001t0001g0199 |
2 | NA18962.hp1 NA18989.hp1 |
intron_variant | MODIFIER | c.277+6916T>C | FMR1NB | ENSG00000176988.9 | transcript | ENST00000370467.8 | protein_coding | 1/5 | chrX | 147988595 | |||||||
chrX:147988630 | T | C | 1 | a0001c0001t0001g0058 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.277+6951T>C | FMR1NB | ENSG00000176988.9 | transcript | ENST00000370467.8 | protein_coding | 1/5 | chrX | 147988630 | |||||||
chrX:147988973 | G | A | 1 | a0002c0002t0001g0114 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.277+7294G>A | FMR1NB | ENSG00000176988.9 | transcript | ENST00000370467.8 | protein_coding | 1/5 | chrX | 147988973 | |||||||
chrX:147989571 | C | A | 2 | a0002c0002t0001g0024 a0002c0002t0001g0127 |
3 | HG01884.hp2 HG02572.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.277+7892C>A | FMR1NB | ENSG00000176988.9 | transcript | ENST00000370467.8 | protein_coding | 1/5 | chrX | 147989571 | |||||||
chrX:147989575 | A | G | 40 | a0001c0001t0001g0004 a0001c0001t0001g0012 a0001c0001t0001g0034 others(37): Show |
49 | HG00639.hp1 HG01168.hp1 HG01243.hp1 others(46): Show |
intron_variant | MODIFIER | c.277+7896A>G | FMR1NB | ENSG00000176988.9 | transcript | ENST00000370467.8 | protein_coding | 1/5 | chrX | 147989575 | |||||||
chrX:147989605 | A | G | 1 | a0001c0001t0001g0090 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.277+7926A>G | FMR1NB | ENSG00000176988.9 | transcript | ENST00000370467.8 | protein_coding | 1/5 | chrX | 147989605 | |||||||
chrX:147989611 | C | T | 7 | a0002c0002t0001g0016 a0002c0002t0001g0114 a0002c0002t0001g0163 others(4): Show |
9 | HG00639.hp2 HG01123.hp1 HG01258.hp1 others(6): Show |
intron_variant | MODIFIER | c.277+7932C>T | FMR1NB | ENSG00000176988.9 | transcript | ENST00000370467.8 | protein_coding | 1/5 | chrX | 147989611 | |||||||
chrX:147989615 | G | A | 2 | a0001c0001t0001g0025 a0002c0002t0001g0171 |
3 | HG01884.hp1 HG02109.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.277+7936G>A | FMR1NB | ENSG00000176988.9 | transcript | ENST00000370467.8 | protein_coding | 1/5 | chrX | 147989615 | |||||||
chrX:147989621 | C | T | 35 | a0001c0001t0001g0004 a0001c0001t0001g0047 a0001c0001t0001g0094 others(32): Show |
42 | HG00639.hp1 HG01168.hp1 HG01243.hp1 others(39): Show |
intron_variant | MODIFIER | c.277+7942C>T | FMR1NB | ENSG00000176988.9 | transcript | ENST00000370467.8 | protein_coding | 1/5 | chrX | 147989621 | |||||||
chrX:147989655 | C | T | 40 | a0001c0001t0001g0004 a0001c0001t0001g0012 a0001c0001t0001g0034 others(37): Show |
49 | HG00639.hp1 HG01168.hp1 HG01243.hp1 others(46): Show |
intron_variant | MODIFIER | c.277+7976C>T | FMR1NB | ENSG00000176988.9 | transcript | ENST00000370467.8 | protein_coding | 1/5 | chrX | 147989655 | |||||||
chrX:147989757 | T | C | 133 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(130): Show |
181 | HG00323.hp1 HG00408.hp1 HG00438.hp2 others(178): Show |
intron_variant | MODIFIER | c.277+8078T>C | FMR1NB | ENSG00000176988.9 | transcript | ENST00000370467.8 | protein_coding | 1/5 | chrX | 147989757 | |||||||
chrX:147989823 | C | T | 13 | a0001c0001t0001g0002 a0001c0001t0001g0025 a0001c0001t0001g0026 others(10): Show |
21 | HG01069.hp1 HG01071.hp2 HG01123.hp2 others(18): Show |
intron_variant | MODIFIER | c.277+8144C>T | FMR1NB | ENSG00000176988.9 | transcript | ENST00000370467.8 | protein_coding | 1/5 | chrX | 147989823 | |||||||
chrX:147989874 | C | T | 40 | a0001c0001t0001g0004 a0001c0001t0001g0012 a0001c0001t0001g0034 others(37): Show |
49 | HG00639.hp1 HG01168.hp1 HG01243.hp1 others(46): Show |
intron_variant | MODIFIER | c.277+8195C>T | FMR1NB | ENSG00000176988.9 | transcript | ENST00000370467.8 | protein_coding | 1/5 | chrX | 147989874 | |||||||
chrX:147990039 | GA | G | 85 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(82): Show |
124 | HG00323.hp1 HG00408.hp1 HG00438.hp2 others(121): Show |
intron_variant | MODIFIER | c.277+8376delA | FMR1NB | ENSG00000176988.9 | transcript | ENST00000370467.8 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chrX | 147990039 | ||||||
chrX:147990039 | GAA | G | 38 | a0001c0001t0001g0004 a0001c0001t0001g0012 a0001c0001t0001g0034 others(35): Show |
47 | HG00639.hp1 HG01168.hp1 HG01243.hp1 others(44): Show |
intron_variant | MODIFIER | c.277+8375_277+8376d others(4): Show |
FMR1NB | ENSG00000176988.9 | transcript | ENST00000370467.8 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chrX | 147990039 | ||||||
chrX:147990041 | A | G | 1 | a0002c0002t0001g0104 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.277+8362A>G | FMR1NB | ENSG00000176988.9 | transcript | ENST00000370467.8 | protein_coding | 1/5 | chrX | 147990041 | |||||||
chrX:147990122 | G | A | 2 | a0001c0001t0001g0034 a0001c0001t0001g0109 |
2 | HG02486.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.277+8443G>A | FMR1NB | ENSG00000176988.9 | transcript | ENST00000370467.8 | protein_coding | 1/5 | chrX | 147990122 | |||||||
chrX:147990640 | AAAAC | A | 5 | a0001c0001t0001g0012 a0001c0001t0001g0034 a0001c0001t0001g0108 others(2): Show |
7 | HG02486.hp1 HG02559.hp2 HG02970.hp2 others(4): Show |
intron_variant | MODIFIER | c.277+8965_277+8968d others(6): Show |
FMR1NB | ENSG00000176988.9 | transcript | ENST00000370467.8 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chrX | 147990640 | ||||||
chrX:147990830 | C | G | 1 | a0002c0002t0001g0051 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.277+9151C>G | FMR1NB | ENSG00000176988.9 | transcript | ENST00000370467.8 | protein_coding | 1/5 | chrX | 147990830 | |||||||
chrX:147990884 | A | G | 118 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(115): Show |
158 | HG00323.hp1 HG00408.hp1 HG00438.hp2 others(155): Show |
intron_variant | MODIFIER | c.277+9205A>G | FMR1NB | ENSG00000176988.9 | transcript | ENST00000370467.8 | protein_coding | 1/5 | chrX | 147990884 | |||||||
chrX:147991203 | C | T | 1 | a0001c0001t0001g0183 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.277+9524C>T | FMR1NB | ENSG00000176988.9 | transcript | ENST00000370467.8 | protein_coding | 1/5 | chrX | 147991203 | |||||||
chrX:147991227 | T | C | 135 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(132): Show |
183 | HG00323.hp1 HG00408.hp1 HG00438.hp2 others(180): Show |
intron_variant | MODIFIER | c.277+9548T>C | FMR1NB | ENSG00000176988.9 | transcript | ENST00000370467.8 | protein_coding | 1/5 | chrX | 147991227 | |||||||
chrX:147991615 | T | C | 135 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(132): Show |
183 | HG00323.hp1 HG00408.hp1 HG00438.hp2 others(180): Show |
intron_variant | MODIFIER | c.277+9936T>C | FMR1NB | ENSG00000176988.9 | transcript | ENST00000370467.8 | protein_coding | 1/5 | chrX | 147991615 | |||||||
chrX:147991642 | T | G | 9 | a0001c0001t0001g0004 a0001c0001t0001g0047 a0001c0001t0001g0094 others(6): Show |
13 | HG00639.hp1 HG01891.hp1 HG02257.hp1 others(10): Show |
intron_variant | MODIFIER | c.277+9963T>G | FMR1NB | ENSG00000176988.9 | transcript | ENST00000370467.8 | protein_coding | 1/5 | chrX | 147991642 | |||||||
chrX:147991646 | T | C | 1 | a0001c0001t0001g0120 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.277+9967T>C | FMR1NB | ENSG00000176988.9 | transcript | ENST00000370467.8 | protein_coding | 1/5 | chrX | 147991646 | |||||||
chrX:147991647 | C | CTTTTTT | 5 | a0001c0001t0001g0034 a0001c0001t0001g0109 a0002c0002t0001g0052 others(2): Show |
5 | HG02257.hp1 HG02486.hp1 HG02965.hp1 others(2): Show |
intron_variant | MODIFIER | c.277+9980_277+9985d others(8): Show |
FMR1NB | ENSG00000176988.9 | transcript | ENST00000370467.8 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chrX | 147991647 | ||||||
chrX:147991647 | C | CTTTTTTT | 21 | a0001c0001t0001g0004 a0001c0001t0001g0012 a0001c0001t0001g0047 others(18): Show |
30 | HG00639.hp1 HG01891.hp1 HG02258.hp1 others(27): Show |
intron_variant | MODIFIER | c.277+9979_277+9985d others(9): Show |
FMR1NB | ENSG00000176988.9 | transcript | ENST00000370467.8 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chrX | 147991647 | ||||||
chrX:147991647 | C | CTTTTTTT others(1): Show |
7 | a0002c0002t0001g0100 a0002c0002t0001g0101 a0002c0002t0001g0102 others(4): Show |
7 | HG01168.hp1 HG02622.hp2 HG02723.hp1 others(4): Show |
intron_variant | MODIFIER | c.277+9978_277+9985d others(10): Show |
FMR1NB | ENSG00000176988.9 | transcript | ENST00000370467.8 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chrX | 147991647 | ||||||
chrX:147991647 | C | CTTTTTTT others(2): Show |
6 | a0002c0002t0001g0035 a0002c0002t0001g0036 a0002c0002t0001g0037 others(3): Show |
6 | HG01243.hp1 HG02451.hp2 HG02647.hp1 others(3): Show |
intron_variant | MODIFIER | c.277+9977_277+9985d others(11): Show |
FMR1NB | ENSG00000176988.9 | transcript | ENST00000370467.8 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chrX | 147991647 | ||||||
chrX:147991647 | C | T | 1 | a0001c0001t0001g0120 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.277+9968C>T | FMR1NB | ENSG00000176988.9 | transcript | ENST00000370467.8 | protein_coding | 1/5 | chrX | 147991647 | |||||||
chrX:147991647 | CT | C | 18 | a0001c0001t0001g0041 a0001c0001t0001g0057 a0001c0001t0001g0063 others(15): Show |
18 | HG00099.hp2 HG01074.hp1 HG01099.hp1 others(15): Show |
intron_variant | MODIFIER | c.277+9985delT | FMR1NB | ENSG00000176988.9 | transcript | ENST00000370467.8 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chrX | 147991647 | ||||||
chrX:147991647 | CTT | C | 17 | a0001c0001t0001g0005 a0001c0001t0001g0027 a0001c0001t0001g0028 others(14): Show |
24 | HG01168.hp2 HG01169.hp1 HG02080.hp1 others(21): Show |
intron_variant | MODIFIER | c.277+9984_277+9985d others(4): Show |
FMR1NB | ENSG00000176988.9 | transcript | ENST00000370467.8 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chrX | 147991647 | ||||||
chrX:147991648 | T | C | 1 | a0001c0001t0001g0120 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.277+9969T>C | FMR1NB | ENSG00000176988.9 | transcript | ENST00000370467.8 | protein_coding | 1/5 | chrX | 147991648 | |||||||
chrX:147991775 | C | A | 1 | a0002c0002t0001g0036 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.277+10096C>A | FMR1NB | ENSG00000176988.9 | transcript | ENST00000370467.8 | protein_coding | 1/5 | chrX | 147991775 | |||||||
chrX:147991810 | C | T | 15 | a0001c0001t0001g0005 a0001c0001t0001g0027 a0001c0001t0001g0028 others(12): Show |
22 | HG01168.hp2 HG01169.hp1 HG02080.hp1 others(19): Show |
intron_variant | MODIFIER | c.277+10131C>T | FMR1NB | ENSG00000176988.9 | transcript | ENST00000370467.8 | protein_coding | 1/5 | chrX | 147991810 | |||||||
chrX:147991912 | C | T | 4 | a0002c0002t0001g0099 a0002c0002t0001g0103 a0002c0002t0001g0104 others(1): Show |
4 | HG02451.hp1 HG02622.hp2 HG02723.hp1 others(1): Show |
intron_variant | MODIFIER | c.277+10233C>T | FMR1NB | ENSG00000176988.9 | transcript | ENST00000370467.8 | protein_coding | 1/5 | chrX | 147991912 | |||||||
chrX:147991951 | G | C | 1 | a0002c0002t0001g0134 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.277+10272G>C | FMR1NB | ENSG00000176988.9 | transcript | ENST00000370467.8 | protein_coding | 1/5 | chrX | 147991951 | |||||||
chrX:147992007 | G | A | 1 | a0002c0002t0001g0135 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.277+10328G>A | FMR1NB | ENSG00000176988.9 | transcript | ENST00000370467.8 | protein_coding | 1/5 | chrX | 147992007 | |||||||
chrX:147992080 | T | C | 135 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(132): Show |
183 | HG00323.hp1 HG00408.hp1 HG00438.hp2 others(180): Show |
intron_variant | MODIFIER | c.277+10401T>C | FMR1NB | ENSG00000176988.9 | transcript | ENST00000370467.8 | protein_coding | 1/5 | chrX | 147992080 | |||||||
chrX:147992134 | T | C | 135 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(132): Show |
183 | HG00323.hp1 HG00408.hp1 HG00438.hp2 others(180): Show |
intron_variant | MODIFIER | c.277+10455T>C | FMR1NB | ENSG00000176988.9 | transcript | ENST00000370467.8 | protein_coding | 1/5 | chrX | 147992134 | |||||||
chrX:147992149 | G | A | 1 | a0002c0002t0001g0112 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.277+10470G>A | FMR1NB | ENSG00000176988.9 | transcript | ENST00000370467.8 | protein_coding | 1/5 | chrX | 147992149 | |||||||
chrX:147992176 | C | A | 1 | a0001c0001t0001g0120 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.277+10497C>A | FMR1NB | ENSG00000176988.9 | transcript | ENST00000370467.8 | protein_coding | 1/5 | chrX | 147992176 | |||||||
chrX:147992177 | A | C | 1 | a0001c0001t0001g0120 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.277+10498A>C | FMR1NB | ENSG00000176988.9 | transcript | ENST00000370467.8 | protein_coding | 1/5 | chrX | 147992177 | |||||||
chrX:147992178 | C | A | 1 | a0001c0001t0001g0120 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.277+10499C>A | FMR1NB | ENSG00000176988.9 | transcript | ENST00000370467.8 | protein_coding | 1/5 | chrX | 147992178 | |||||||
chrX:147992187 | C | A | 1 | a0001c0001t0001g0120 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.277+10508C>A | FMR1NB | ENSG00000176988.9 | transcript | ENST00000370467.8 | protein_coding | 1/5 | chrX | 147992187 | |||||||
chrX:147992232 | T | C | 40 | a0001c0001t0001g0004 a0001c0001t0001g0012 a0001c0001t0001g0034 others(37): Show |
49 | HG00639.hp1 HG01168.hp1 HG01243.hp1 others(46): Show |
intron_variant | MODIFIER | c.277+10553T>C | FMR1NB | ENSG00000176988.9 | transcript | ENST00000370467.8 | protein_coding | 1/5 | chrX | 147992232 | |||||||
chrX:147992236 | T | C | 40 | a0001c0001t0001g0004 a0001c0001t0001g0012 a0001c0001t0001g0034 others(37): Show |
49 | HG00639.hp1 HG01168.hp1 HG01243.hp1 others(46): Show |
intron_variant | MODIFIER | c.277+10557T>C | FMR1NB | ENSG00000176988.9 | transcript | ENST00000370467.8 | protein_coding | 1/5 | chrX | 147992236 | |||||||
chrX:147992260 | C | T | 13 | a0001c0001t0001g0002 a0001c0001t0001g0025 a0001c0001t0001g0026 others(10): Show |
21 | HG01069.hp1 HG01071.hp2 HG01123.hp2 others(18): Show |
intron_variant | MODIFIER | c.277+10581C>T | FMR1NB | ENSG00000176988.9 | transcript | ENST00000370467.8 | protein_coding | 1/5 | chrX | 147992260 | |||||||
chrX:147992270 | G | A | 4 | a0002c0002t0001g0093 a0002c0002t0001g0111 a0002c0002t0001g0112 others(1): Show |
4 | HG02257.hp1 HG02965.hp1 HG02976.hp1 others(1): Show |
intron_variant | MODIFIER | c.277+10591G>A | FMR1NB | ENSG00000176988.9 | transcript | ENST00000370467.8 | protein_coding | 1/5 | chrX | 147992270 | |||||||
chrX:147992282 | A | AG | 56 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0006 others(53): Show |
80 | HG00323.hp1 HG00408.hp1 HG00438.hp2 others(77): Show |
intron_variant | MODIFIER | c.277+10609dupG | FMR1NB | ENSG00000176988.9 | transcript | ENST00000370467.8 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chrX | 147992282 | ||||||
chrX:147992333 | A | G | 95 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(92): Show |
134 | HG00323.hp1 HG00408.hp1 HG00438.hp2 others(131): Show |
intron_variant | MODIFIER | c.277+10654A>G | FMR1NB | ENSG00000176988.9 | transcript | ENST00000370467.8 | protein_coding | 1/5 | chrX | 147992333 | |||||||
chrX:147992368 | C | T | 56 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0006 others(53): Show |
80 | HG00323.hp1 HG00408.hp1 HG00438.hp2 others(77): Show |
intron_variant | MODIFIER | c.277+10689C>T | FMR1NB | ENSG00000176988.9 | transcript | ENST00000370467.8 | protein_coding | 1/5 | chrX | 147992368 | |||||||
chrX:147992424 | A | ACCCCTCA others(507): Show |
1 | a0001c0001t0001g0120 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.277+10758_277+1075 others(518): Show |
FMR1NB | ENSG00000176988.9 | transcript | ENST00000370467.8 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chrX | 147992424 | ||||||
chrX:147992424 | A | G | 40 | a0001c0001t0001g0004 a0001c0001t0001g0012 a0001c0001t0001g0034 others(37): Show |
49 | HG00639.hp1 HG01168.hp1 HG01243.hp1 others(46): Show |
intron_variant | MODIFIER | c.277+10745A>G | FMR1NB | ENSG00000176988.9 | transcript | ENST00000370467.8 | protein_coding | 1/5 | chrX | 147992424 | |||||||
chrX:147992438 | A | G | 210 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(207): Show |
272 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(269): Show |
intron_variant | MODIFIER | c.277+10759A>G | FMR1NB | ENSG00000176988.9 | transcript | ENST00000370467.8 | protein_coding | 1/5 | chrX | 147992438 | |||||||
chrX:147992454 | C | CGGGTGGG others(1225): Show |
3 | a0002c0002t0001g0111 a0002c0002t0001g0112 a0002c0002t0001g0212 |
3 | HG02965.hp1 HG02976.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.278-10744_278-1074 others(1236): Show |
FMR1NB | ENSG00000176988.9 | transcript | ENST00000370467.8 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chrX | 147992454 | ||||||
chrX:147992457 | G | GT | 37 | a0001c0001t0001g0004 a0001c0001t0001g0012 a0001c0001t0001g0034 others(34): Show |
46 | HG00639.hp1 HG01168.hp1 HG01243.hp1 others(43): Show |
intron_variant | MODIFIER | c.278-10744_278-1074 others(5): Show |
FMR1NB | ENSG00000176988.9 | transcript | ENST00000370467.8 | protein_coding | 1/5 | chrX | 147992457 | |||||||
chrX:147992458 | C | CG | 94 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(91): Show |
133 | HG00323.hp1 HG00408.hp1 HG00438.hp2 others(130): Show |
intron_variant | MODIFIER | c.278-10741dupG | FMR1NB | ENSG00000176988.9 | transcript | ENST00000370467.8 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chrX | 147992458 | ||||||
chrX:147992458 | C | CGGGGGGG others(773): Show |
1 | a0002c0002t0001g0138 | 1 | NA19065.hp2 | intron_variant | MODIFIER | c.278-10741_278-1074 others(784): Show |
FMR1NB | ENSG00000176988.9 | transcript | ENST00000370467.8 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chrX | 147992458 | ||||||
chrX:147992458 | C | CGGGGGGG others(947): Show |
1 | a0002c0002t0001g0119 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.278-10741_278-1074 others(958): Show |
FMR1NB | ENSG00000176988.9 | transcript | ENST00000370467.8 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chrX | 147992458 | ||||||
chrX:147992458 | C | CGGGGGGG others(951): Show |
2 | a0002c0002t0001g0169 a0002c0002t0001g0170 |
2 | NA18942.hp2 NA18947.hp1 |
intron_variant | MODIFIER | c.278-10741_278-1074 others(962): Show |
FMR1NB | ENSG00000176988.9 | transcript | ENST00000370467.8 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chrX | 147992458 | ||||||
chrX:147992458 | C | CGGGGGGG others(773): Show |
1 | a0002c0002t0001g0139 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.278-10741_278-1074 others(784): Show |
FMR1NB | ENSG00000176988.9 | transcript | ENST00000370467.8 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chrX | 147992458 | ||||||
chrX:147992458 | C | CGGGGGGG others(773): Show |
1 | a0002c0002t0001g0140 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.278-10741_278-1074 others(784): Show |
FMR1NB | ENSG00000176988.9 | transcript | ENST00000370467.8 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chrX | 147992458 | ||||||
chrX:147992458 | C | CGGGGGGG others(773): Show |
1 | a0002c0002t0001g0122 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.278-10741_278-1074 others(784): Show |
FMR1NB | ENSG00000176988.9 | transcript | ENST00000370467.8 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chrX | 147992458 | ||||||
chrX:147992458 | C | CGGGGGGG others(772): Show |
1 | a0002c0002t0001g0177 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.278-10741_278-1074 others(783): Show |
FMR1NB | ENSG00000176988.9 | transcript | ENST00000370467.8 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chrX | 147992458 | ||||||
chrX:147992458 | C | CGGGGGGG others(773): Show |
53 | a0002c0002t0001g0007 a0002c0002t0001g0013 a0002c0002t0001g0014 others(50): Show |
67 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(64): Show |
intron_variant | MODIFIER | c.278-10741_278-1074 others(784): Show |
FMR1NB | ENSG00000176988.9 | transcript | ENST00000370467.8 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chrX | 147992458 | ||||||
chrX:147992458 | C | CGGGGGGG others(773): Show |
2 | a0002c0002t0001g0173 a0002c0002t0001g0174 |
2 | HG00140.hp1 HG01071.hp1 |
intron_variant | MODIFIER | c.278-10741_278-1074 others(784): Show |
FMR1NB | ENSG00000176988.9 | transcript | ENST00000370467.8 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chrX | 147992458 | ||||||
chrX:147992458 | C | CGGGGGGG others(774): Show |
1 | a0002c0002t0001g0033 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.278-10741_278-1074 others(785): Show |
FMR1NB | ENSG00000176988.9 | transcript | ENST00000370467.8 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chrX | 147992458 | ||||||
chrX:147992458 | C | CGGGGGGG others(774): Show |
1 | a0002c0002t0001g0157 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.278-10741_278-1074 others(785): Show |
FMR1NB | ENSG00000176988.9 | transcript | ENST00000370467.8 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chrX | 147992458 | ||||||
chrX:147992458 | C | CGGGGGGG others(778): Show |
1 | a0002c0002t0001g0158 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.278-10741_278-1074 others(789): Show |
FMR1NB | ENSG00000176988.9 | transcript | ENST00000370467.8 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chrX | 147992458 | ||||||
chrX:147992458 | C | CGGGGGGG others(775): Show |
1 | a0002c0002t0001g0126 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.278-10741_278-1074 others(786): Show |
FMR1NB | ENSG00000176988.9 | transcript | ENST00000370467.8 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chrX | 147992458 | ||||||
chrX:147992458 | C | CGGGGGGG others(774): Show |
4 | a0002c0002t0001g0159 a0002c0002t0001g0160 a0002c0002t0001g0161 others(1): Show |
4 | HG00642.hp1 HG01175.hp1 HG01175.hp2 others(1): Show |
intron_variant | MODIFIER | c.278-10741_278-1074 others(785): Show |
FMR1NB | ENSG00000176988.9 | transcript | ENST00000370467.8 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chrX | 147992458 | ||||||
chrX:147992458 | C | CGGGGGGG others(775): Show |
1 | a0002c0002t0001g0167 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.278-10741_278-1074 others(786): Show |
FMR1NB | ENSG00000176988.9 | transcript | ENST00000370467.8 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chrX | 147992458 | ||||||
chrX:147992458 | C | CGGGGGGG others(774): Show |
2 | a0002c0002t0001g0030 a0002c0002t0001g0162 |
2 | HG04115.hp1 HG04204.hp1 |
intron_variant | MODIFIER | c.278-10741_278-1074 others(785): Show |
FMR1NB | ENSG00000176988.9 | transcript | ENST00000370467.8 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chrX | 147992458 | ||||||
chrX:147992458 | C | G | 37 | a0001c0001t0001g0004 a0001c0001t0001g0012 a0001c0001t0001g0034 others(34): Show |
46 | HG00639.hp1 HG01168.hp1 HG01243.hp1 others(43): Show |
intron_variant | MODIFIER | c.278-10743C>G | FMR1NB | ENSG00000176988.9 | transcript | ENST00000370467.8 | protein_coding | 1/5 | chrX | 147992458 | |||||||
chrX:147992461 | A | G | 210 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(207): Show |
272 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(269): Show |
intron_variant | MODIFIER | c.278-10740A>G | FMR1NB | ENSG00000176988.9 | transcript | ENST00000370467.8 | protein_coding | 1/5 | chrX | 147992461 | |||||||
chrX:147992463 | T | G | 137 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(134): Show |
185 | HG00323.hp1 HG00408.hp1 HG00438.hp2 others(182): Show |
intron_variant | MODIFIER | c.278-10738T>G | FMR1NB | ENSG00000176988.9 | transcript | ENST00000370467.8 | protein_coding | 1/5 | chrX | 147992463 | |||||||
chrX:147992468 | AC | A | 74 | a0002c0002t0001g0007 a0002c0002t0001g0013 a0002c0002t0001g0014 others(71): Show |
88 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(85): Show |
intron_variant | MODIFIER | c.278-10726delC | FMR1NB | ENSG00000176988.9 | transcript | ENST00000370467.8 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chrX | 147992468 | ||||||
chrX:147992469 | C | CCCCCCCC others(770): Show |
5 | a0001c0001t0001g0005 a0001c0001t0001g0027 a0001c0001t0001g0194 others(2): Show |
8 | NA18941.hp2 NA18942.hp1 NA18948.hp1 others(5): Show |
intron_variant | MODIFIER | c.278-10726_278-1072 others(781): Show |
FMR1NB | ENSG00000176988.9 | transcript | ENST00000370467.8 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chrX | 147992469 | ||||||
chrX:147992469 | C | CCCCCCCC others(771): Show |
1 | a0001c0001t0001g0005 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.278-10726_278-1072 others(782): Show |
FMR1NB | ENSG00000176988.9 | transcript | ENST00000370467.8 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chrX | 147992469 | ||||||
chrX:147992469 | C | CCCCCCCC others(997): Show |
1 | a0001c0001t0001g0027 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.278-10726_278-1072 others(1008): Show |
FMR1NB | ENSG00000176988.9 | transcript | ENST00000370467.8 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chrX | 147992469 | ||||||
chrX:147992469 | C | CCCCCCCC others(771): Show |
13 | a0001c0001t0001g0005 a0001c0001t0001g0028 a0001c0001t0001g0061 others(10): Show |
14 | HG01168.hp2 HG01169.hp1 HG02630.hp2 others(11): Show |
intron_variant | MODIFIER | c.278-10726_278-1072 others(782): Show |
FMR1NB | ENSG00000176988.9 | transcript | ENST00000370467.8 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chrX | 147992469 | ||||||
chrX:147992469 | C | CCCCCCCC others(771): Show |
2 | a0001c0001t0001g0201 a0002c0002t0001g0197 |
2 | HG02809.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.278-10726_278-1072 others(782): Show |
FMR1NB | ENSG00000176988.9 | transcript | ENST00000370467.8 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chrX | 147992469 | ||||||
chrX:147992469 | C | CCCCCCCC others(772): Show |
1 | a0001c0001t0001g0204 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.278-10726_278-1072 others(783): Show |
FMR1NB | ENSG00000176988.9 | transcript | ENST00000370467.8 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chrX | 147992469 | ||||||
chrX:147992469 | C | CCCCCCCC others(771): Show |
2 | a0001c0001t0001g0198 a0001c0001t0001g0199 |
2 | NA18962.hp1 NA18989.hp1 |
intron_variant | MODIFIER | c.278-10726_278-1072 others(782): Show |
FMR1NB | ENSG00000176988.9 | transcript | ENST00000370467.8 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chrX | 147992469 | ||||||
chrX:147992469 | C | CCCCCCCC others(771): Show |
1 | a0001c0001t0001g0183 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.278-10726_278-1072 others(782): Show |
FMR1NB | ENSG00000176988.9 | transcript | ENST00000370467.8 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chrX | 147992469 | ||||||
chrX:147992469 | C | CCCCCCCC others(771): Show |
2 | a0001c0001t0001g0011 a0001c0001t0001g0056 |
2 | NA18966.hp1 NA18992.hp2 |
intron_variant | MODIFIER | c.278-10726_278-1072 others(782): Show |
FMR1NB | ENSG00000176988.9 | transcript | ENST00000370467.8 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chrX | 147992469 | ||||||
chrX:147992469 | C | CCCCCCCC others(772): Show |
1 | a0001c0001t0001g0011 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.278-10726_278-1072 others(783): Show |
FMR1NB | ENSG00000176988.9 | transcript | ENST00000370467.8 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chrX | 147992469 | ||||||
chrX:147992469 | C | CCCCCCCC others(771): Show |
1 | a0002c0002t0001g0182 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.278-10726_278-1072 others(782): Show |
FMR1NB | ENSG00000176988.9 | transcript | ENST00000370467.8 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chrX | 147992469 | ||||||
chrX:147992469 | C | CCCCCCCC others(771): Show |
1 | a0001c0001t0002g0193 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.278-10726_278-1072 others(782): Show |
FMR1NB | ENSG00000176988.9 | transcript | ENST00000370467.8 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chrX | 147992469 | ||||||
chrX:147992469 | C | CCCCCCCC others(771): Show |
14 | a0001c0001t0001g0002 a0001c0001t0001g0025 a0001c0001t0001g0026 others(11): Show |
20 | HG01069.hp1 HG01071.hp2 HG01123.hp2 others(17): Show |
intron_variant | MODIFIER | c.278-10726_278-1072 others(782): Show |
FMR1NB | ENSG00000176988.9 | transcript | ENST00000370467.8 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chrX | 147992469 | ||||||
chrX:147992469 | C | CCCCCCCC others(771): Show |
34 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0006 others(31): Show |
49 | HG00323.hp1 HG00544.hp2 HG00609.hp1 others(46): Show |
intron_variant | MODIFIER | c.278-10726_278-1072 others(782): Show |
FMR1NB | ENSG00000176988.9 | transcript | ENST00000370467.8 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chrX | 147992469 | ||||||
chrX:147992469 | C | CCCCCCCC others(771): Show |
1 | a0001c0001t0001g0075 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.278-10726_278-1072 others(782): Show |
FMR1NB | ENSG00000176988.9 | transcript | ENST00000370467.8 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chrX | 147992469 | ||||||
chrX:147992469 | C | CCCCCCCC others(772): Show |
1 | a0001c0001t0001g0043 | 1 | NA19072.hp1 | intron_variant | MODIFIER | c.278-10726_278-1072 others(783): Show |
FMR1NB | ENSG00000176988.9 | transcript | ENST00000370467.8 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chrX | 147992469 | ||||||
chrX:147992469 | C | CCCCCCCC others(772): Show |
1 | a0001c0001t0001g0003 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.278-10726_278-1072 others(783): Show |
FMR1NB | ENSG00000176988.9 | transcript | ENST00000370467.8 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chrX | 147992469 | ||||||
chrX:147992469 | C | CCCCCCCC others(722): Show |
1 | a0001c0001t0001g0077 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.278-10726_278-1072 others(733): Show |
FMR1NB | ENSG00000176988.9 | transcript | ENST00000370467.8 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chrX | 147992469 | ||||||
chrX:147992469 | C | CCCCCCCC others(772): Show |
1 | a0001c0001t0001g0006 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.278-10726_278-1072 others(783): Show |
FMR1NB | ENSG00000176988.9 | transcript | ENST00000370467.8 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chrX | 147992469 | ||||||
chrX:147992469 | C | CCCCCCCC others(771): Show |
3 | a0001c0001t0001g0029 a0001c0001t0001g0085 a0001c0001t0001g0089 |
3 | HG01074.hp1 HG01975.hp2 NA18953.hp1 |
intron_variant | MODIFIER | c.278-10726_278-1072 others(782): Show |
FMR1NB | ENSG00000176988.9 | transcript | ENST00000370467.8 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chrX | 147992469 | ||||||
chrX:147992469 | C | CCCCCCCC others(772): Show |
1 | a0001c0001t0001g0184 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.278-10726_278-1072 others(783): Show |
FMR1NB | ENSG00000176988.9 | transcript | ENST00000370467.8 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chrX | 147992469 | ||||||
chrX:147992469 | C | CCCCCCCC others(772): Show |
1 | a0001c0001t0001g0090 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.278-10726_278-1072 others(783): Show |
FMR1NB | ENSG00000176988.9 | transcript | ENST00000370467.8 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chrX | 147992469 | ||||||
chrX:147992469 | C | CCCCCCCC others(771): Show |
1 | a0001c0001t0001g0018 | 2 | NA18977.hp1 NA18998.hp2 |
intron_variant | MODIFIER | c.278-10726_278-1072 others(782): Show |
FMR1NB | ENSG00000176988.9 | transcript | ENST00000370467.8 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chrX | 147992469 | ||||||
chrX:147992469 | C | CCCCCCCC others(772): Show |
1 | a0001c0001t0001g0172 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.278-10726_278-1072 others(783): Show |
FMR1NB | ENSG00000176988.9 | transcript | ENST00000370467.8 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chrX | 147992469 | ||||||
chrX:147992469 | C | CCCCCCCC others(772): Show |
1 | a0001c0001t0001g0088 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.278-10726_278-1072 others(783): Show |
FMR1NB | ENSG00000176988.9 | transcript | ENST00000370467.8 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chrX | 147992469 | ||||||
chrX:147992469 | C | CCCCCCCC others(774): Show |
1 | a0001c0001t0001g0176 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.278-10726_278-1072 others(785): Show |
FMR1NB | ENSG00000176988.9 | transcript | ENST00000370467.8 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chrX | 147992469 | ||||||
chrX:147992469 | C | CCCCCCCC others(772): Show |
1 | a0001c0001t0001g0066 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.278-10726_278-1072 others(783): Show |
FMR1NB | ENSG00000176988.9 | transcript | ENST00000370467.8 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chrX | 147992469 | ||||||
chrX:147992469 | C | CCCCCCCC others(776): Show |
1 | a0001c0001t0001g0002 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.278-10726_278-1072 others(787): Show |
FMR1NB | ENSG00000176988.9 | transcript | ENST00000370467.8 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chrX | 147992469 | ||||||
chrX:147992469 | C | CCCCCCCC others(778): Show |
1 | a0001c0001t0001g0021 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.278-10726_278-1072 others(789): Show |
FMR1NB | ENSG00000176988.9 | transcript | ENST00000370467.8 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chrX | 147992469 | ||||||
chrX:147992469 | C | CCCCCCCC others(772): Show |
1 | a0001c0001t0001g0060 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.278-10726_278-1072 others(783): Show |
FMR1NB | ENSG00000176988.9 | transcript | ENST00000370467.8 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chrX | 147992469 | ||||||
chrX:147992469 | C | CCCCCCCC others(773): Show |
1 | a0001c0001t0001g0006 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.278-10726_278-1072 others(784): Show |
FMR1NB | ENSG00000176988.9 | transcript | ENST00000370467.8 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chrX | 147992469 | ||||||
chrX:147992469 | C | CCCCCCCC others(773): Show |
1 | a0001c0001t0001g0067 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.278-10726_278-1072 others(784): Show |
FMR1NB | ENSG00000176988.9 | transcript | ENST00000370467.8 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chrX | 147992469 | ||||||
chrX:147992469 | C | CCCCCCCC others(773): Show |
1 | a0001c0001t0001g0080 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.278-10726_278-1072 others(784): Show |
FMR1NB | ENSG00000176988.9 | transcript | ENST00000370467.8 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chrX | 147992469 | ||||||
chrX:147992469 | C | CCCCCCCC others(774): Show |
1 | a0001c0001t0001g0086 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.278-10726_278-1072 others(785): Show |
FMR1NB | ENSG00000176988.9 | transcript | ENST00000370467.8 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chrX | 147992469 | ||||||
chrX:147992469 | C | CCCCCCCC others(776): Show |
1 | a0001c0001t0001g0059 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.278-10726_278-1072 others(787): Show |
FMR1NB | ENSG00000176988.9 | transcript | ENST00000370467.8 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chrX | 147992469 | ||||||
chrX:147992469 | C | CCCCCCCC others(771): Show |
1 | a0001c0001t0001g0002 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.278-10726_278-1072 others(782): Show |
FMR1NB | ENSG00000176988.9 | transcript | ENST00000370467.8 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chrX | 147992469 | ||||||
chrX:147992469 | C | CCCCCCCC others(1273): Show |
5 | a0001c0001t0001g0012 a0001c0001t0001g0034 a0001c0001t0001g0108 others(2): Show |
7 | HG02486.hp1 HG02559.hp2 HG02970.hp2 others(4): Show |
intron_variant | MODIFIER | c.278-10726_278-1072 others(1284): Show |
FMR1NB | ENSG00000176988.9 | transcript | ENST00000370467.8 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chrX | 147992469 | ||||||
chrX:147992469 | C | CCCCCCCC others(1273): Show |
1 | a0002c0002t0001g0040 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.278-10726_278-1072 others(1284): Show |
FMR1NB | ENSG00000176988.9 | transcript | ENST00000370467.8 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chrX | 147992469 | ||||||
chrX:147992469 | C | CCCCCCCC others(1273): Show |
3 | a0002c0002t0001g0035 a0002c0002t0001g0038 a0002c0002t0001g0039 |
3 | HG01243.hp1 HG02451.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.278-10726_278-1072 others(1284): Show |
FMR1NB | ENSG00000176988.9 | transcript | ENST00000370467.8 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chrX | 147992469 | ||||||
chrX:147992469 | C | CCCCCCCC others(1273): Show |
3 | a0002c0002t0001g0103 a0002c0002t0001g0104 a0002c0002t0001g0113 |
3 | HG02622.hp2 HG02723.hp1 HG02896.hp2 |
intron_variant | MODIFIER | c.278-10726_278-1072 others(1284): Show |
FMR1NB | ENSG00000176988.9 | transcript | ENST00000370467.8 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chrX | 147992469 | ||||||
chrX:147992469 | C | CCCCCCCC others(1273): Show |
5 | a0002c0002t0001g0097 a0002c0002t0001g0100 a0002c0002t0001g0102 others(2): Show |
5 | HG03017.hp1 HG03491.hp1 HG03669.hp2 others(2): Show |
intron_variant | MODIFIER | c.278-10726_278-1072 others(1284): Show |
FMR1NB | ENSG00000176988.9 | transcript | ENST00000370467.8 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chrX | 147992469 | ||||||
chrX:147992469 | C | CCCCCCCC others(1275): Show |
1 | a0002c0002t0001g0098 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.278-10726_278-1072 others(1286): Show |
FMR1NB | ENSG00000176988.9 | transcript | ENST00000370467.8 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chrX | 147992469 | ||||||
chrX:147992469 | C | CCCCCCCC others(1275): Show |
1 | a0002c0002t0001g0037 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.278-10726_278-1072 others(1286): Show |
FMR1NB | ENSG00000176988.9 | transcript | ENST00000370467.8 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chrX | 147992469 | ||||||
chrX:147992469 | C | CCCCCCCC others(1273): Show |
1 | a0002c0002t0001g0036 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.278-10726_278-1072 others(1284): Show |
FMR1NB | ENSG00000176988.9 | transcript | ENST00000370467.8 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chrX | 147992469 | ||||||
chrX:147992469 | C | CCCCCCCC others(1273): Show |
1 | a0002c0002t0001g0099 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.278-10726_278-1072 others(1284): Show |
FMR1NB | ENSG00000176988.9 | transcript | ENST00000370467.8 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chrX | 147992469 | ||||||
chrX:147992469 | C | CCCCCCCC others(1273): Show |
1 | a0002c0002t0001g0101 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.278-10726_278-1072 others(1284): Show |
FMR1NB | ENSG00000176988.9 | transcript | ENST00000370467.8 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chrX | 147992469 | ||||||
chrX:147992469 | C | CCCCCCCC others(1095): Show |
8 | a0002c0002t0001g0008 a0002c0002t0001g0017 a0002c0002t0001g0048 others(5): Show |
10 | HG02723.hp2 HG02895.hp1 HG03041.hp1 others(7): Show |
intron_variant | MODIFIER | c.278-10726_278-1072 others(1106): Show |
FMR1NB | ENSG00000176988.9 | transcript | ENST00000370467.8 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chrX | 147992469 | ||||||
chrX:147992469 | C | CCCCCCCC others(1096): Show |
1 | a0002c0002t0001g0008 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.278-10726_278-1072 others(1107): Show |
FMR1NB | ENSG00000176988.9 | transcript | ENST00000370467.8 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chrX | 147992469 | ||||||
chrX:147992469 | C | CCCCCCCC others(1096): Show |
1 | a0002c0002t0001g0051 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.278-10726_278-1072 others(1107): Show |
FMR1NB | ENSG00000176988.9 | transcript | ENST00000370467.8 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chrX | 147992469 | ||||||
chrX:147992469 | C | CCCCCCCC others(772): Show |
1 | a0001c0001t0001g0001 | 1 | NA18985.hp2 | intron_variant | MODIFIER | c.278-10726_278-1072 others(783): Show |
FMR1NB | ENSG00000176988.9 | transcript | ENST00000370467.8 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chrX | 147992469 | ||||||
chrX:147992469 | C | CCCCCCCC others(1273): Show |
1 | a0002c0002t0001g0093 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.278-10726_278-1072 others(1284): Show |
FMR1NB | ENSG00000176988.9 | transcript | ENST00000370467.8 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chrX | 147992469 | ||||||
chrX:147992469 | C | CCCCCCCC others(1273): Show |
5 | a0001c0001t0001g0004 a0001c0001t0001g0047 a0001c0001t0001g0094 others(2): Show |
9 | HG00639.hp1 HG01891.hp1 HG02280.hp2 others(6): Show |
intron_variant | MODIFIER | c.278-10726_278-1072 others(1284): Show |
FMR1NB | ENSG00000176988.9 | transcript | ENST00000370467.8 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chrX | 147992469 | ||||||
chrX:147992469 | C | CCCCCCCC others(772): Show |
1 | a0001c0001t0001g0057 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.278-10726_278-1072 others(783): Show |
FMR1NB | ENSG00000176988.9 | transcript | ENST00000370467.8 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chrX | 147992469 | ||||||
chrX:147992469 | C | CCCCCCCC others(773): Show |
1 | a0001c0001t0001g0001 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.278-10726_278-1072 others(784): Show |
FMR1NB | ENSG00000176988.9 | transcript | ENST00000370467.8 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chrX | 147992469 | ||||||
chrX:147992485 | C | CCGGACGG others(275): Show |
1 | a0001c0001t0001g0120 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.278-10706_278-1070 others(286): Show |
FMR1NB | ENSG00000176988.9 | transcript | ENST00000370467.8 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chrX | 147992485 | ||||||
chrX:147992486 | C | T | 1 | a0001c0001t0001g0195 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.278-10715C>T | FMR1NB | ENSG00000176988.9 | transcript | ENST00000370467.8 | protein_coding | 1/5 | chrX | 147992486 | |||||||
chrX:147992496 | A | G | 43 | a0001c0001t0001g0004 a0001c0001t0001g0012 a0001c0001t0001g0034 others(40): Show |
52 | HG00408.hp1 HG00544.hp1 HG00639.hp1 others(49): Show |
intron_variant | MODIFIER | c.278-10705A>G | FMR1NB | ENSG00000176988.9 | transcript | ENST00000370467.8 | protein_coding | 1/5 | chrX | 147992496 | |||||||
chrX:147992501 | G | A | 1 | a0002c0002t0001g0123 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.278-10700G>A | FMR1NB | ENSG00000176988.9 | transcript | ENST00000370467.8 | protein_coding | 1/5 | chrX | 147992501 | |||||||
chrX:147992507 | CG | C | 51 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0006 others(48): Show |
75 | HG00323.hp1 HG00438.hp2 HG00544.hp2 others(72): Show |
intron_variant | MODIFIER | c.278-10688delG | FMR1NB | ENSG00000176988.9 | transcript | ENST00000370467.8 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chrX | 147992507 | ||||||
chrX:147992518 | C | CACCCCCA others(720): Show |
3 | a0001c0001t0001g0055 a0001c0001t0001g0064 a0001c0001t0001g0082 |
3 | HG00408.hp1 HG00544.hp1 NA18960.hp1 |
intron_variant | MODIFIER | c.278-10683_278-1068 others(731): Show |
FMR1NB | ENSG00000176988.9 | transcript | ENST00000370467.8 | protein_coding | 1/5 | chrX | 147992518 | |||||||
chrX:147992519 | C | A | 3 | a0001c0001t0001g0055 a0001c0001t0001g0064 a0001c0001t0001g0082 |
3 | HG00408.hp1 HG00544.hp1 NA18960.hp1 |
intron_variant | MODIFIER | c.278-10682C>A | FMR1NB | ENSG00000176988.9 | transcript | ENST00000370467.8 | protein_coding | 1/5 | chrX | 147992519 | |||||||
chrX:147992540 | C | T | 1 | a0001c0001t0001g0080 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.278-10661C>T | FMR1NB | ENSG00000176988.9 | transcript | ENST00000370467.8 | protein_coding | 1/5 | chrX | 147992540 | |||||||
chrX:147992557 | G | A | 5 | a0001c0001t0001g0012 a0001c0001t0001g0034 a0001c0001t0001g0108 others(2): Show |
7 | HG02486.hp1 HG02559.hp2 HG02970.hp2 others(4): Show |
intron_variant | MODIFIER | c.278-10644G>A | FMR1NB | ENSG00000176988.9 | transcript | ENST00000370467.8 | protein_coding | 1/5 | chrX | 147992557 | |||||||
chrX:147992583 | G | T | 5 | a0001c0001t0001g0012 a0001c0001t0001g0034 a0001c0001t0001g0108 others(2): Show |
7 | HG02486.hp1 HG02559.hp2 HG02970.hp2 others(4): Show |
intron_variant | MODIFIER | c.278-10618G>T | FMR1NB | ENSG00000176988.9 | transcript | ENST00000370467.8 | protein_coding | 1/5 | chrX | 147992583 | |||||||
chrX:147992620 | C | T | 1 | a0002c0002t0001g0156 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.278-10581C>T | FMR1NB | ENSG00000176988.9 | transcript | ENST00000370467.8 | protein_coding | 1/5 | chrX | 147992620 | |||||||
chrX:147992632 | C | T | 1 | a0002c0002t0001g0155 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.278-10569C>T | FMR1NB | ENSG00000176988.9 | transcript | ENST00000370467.8 | protein_coding | 1/5 | chrX | 147992632 | |||||||
chrX:147992633 | G | A | 1 | a0002c0002t0001g0093 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.278-10568G>A | FMR1NB | ENSG00000176988.9 | transcript | ENST00000370467.8 | protein_coding | 1/5 | chrX | 147992633 | |||||||
chrX:147992636 | C | G | 4 | a0002c0002t0001g0015 a0002c0002t0001g0133 a0002c0002t0001g0154 others(1): Show |
6 | HG00099.hp1 HG00280.hp1 HG01175.hp2 others(3): Show |
intron_variant | MODIFIER | c.278-10565C>G | FMR1NB | ENSG00000176988.9 | transcript | ENST00000370467.8 | protein_coding | 1/5 | chrX | 147992636 | |||||||
chrX:147992638 | G | A | 35 | a0001c0001t0001g0004 a0001c0001t0001g0047 a0001c0001t0001g0094 others(32): Show |
42 | HG00639.hp1 HG01168.hp1 HG01243.hp1 others(39): Show |
intron_variant | MODIFIER | c.278-10563G>A | FMR1NB | ENSG00000176988.9 | transcript | ENST00000370467.8 | protein_coding | 1/5 | chrX | 147992638 | |||||||
chrX:147992661 | G | A | 2 | a0002c0002t0001g0104 a0002c0002t0001g0113 |
2 | HG02723.hp1 HG02896.hp2 |
intron_variant | MODIFIER | c.278-10540G>A | FMR1NB | ENSG00000176988.9 | transcript | ENST00000370467.8 | protein_coding | 1/5 | chrX | 147992661 | |||||||
chrX:147992700 | C | T | 1 | a0001c0001t0001g0183 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.278-10501C>T | FMR1NB | ENSG00000176988.9 | transcript | ENST00000370467.8 | protein_coding | 1/5 | chrX | 147992700 | |||||||
chrX:147992719 | C | T | 2 | a0002c0002t0001g0117 a0002c0002t0001g0153 |
2 | HG00408.hp2 HG02523.hp2 |
intron_variant | MODIFIER | c.278-10482C>T | FMR1NB | ENSG00000176988.9 | transcript | ENST00000370467.8 | protein_coding | 1/5 | chrX | 147992719 | |||||||
chrX:147992738 | A | G | 5 | a0001c0001t0001g0012 a0001c0001t0001g0034 a0001c0001t0001g0108 others(2): Show |
7 | HG02486.hp1 HG02559.hp2 HG02970.hp2 others(4): Show |
intron_variant | MODIFIER | c.278-10463A>G | FMR1NB | ENSG00000176988.9 | transcript | ENST00000370467.8 | protein_coding | 1/5 | chrX | 147992738 | |||||||
chrX:147992749 | C | A | 2 | a0002c0002t0001g0104 a0002c0002t0001g0113 |
2 | HG02723.hp1 HG02896.hp2 |
intron_variant | MODIFIER | c.278-10452C>A | FMR1NB | ENSG00000176988.9 | transcript | ENST00000370467.8 | protein_coding | 1/5 | chrX | 147992749 | |||||||
chrX:147992814 | T | C | 210 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(207): Show |
272 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(269): Show |
intron_variant | MODIFIER | c.278-10387T>C | FMR1NB | ENSG00000176988.9 | transcript | ENST00000370467.8 | protein_coding | 1/5 | chrX | 147992814 | |||||||
chrX:147992821 | T | C | 40 | a0001c0001t0001g0004 a0001c0001t0001g0012 a0001c0001t0001g0034 others(37): Show |
49 | HG00639.hp1 HG01168.hp1 HG01243.hp1 others(46): Show |
intron_variant | MODIFIER | c.278-10380T>C | FMR1NB | ENSG00000176988.9 | transcript | ENST00000370467.8 | protein_coding | 1/5 | chrX | 147992821 | |||||||
chrX:147992822 | G | A | 40 | a0001c0001t0001g0004 a0001c0001t0001g0012 a0001c0001t0001g0034 others(37): Show |
49 | HG00639.hp1 HG01168.hp1 HG01243.hp1 others(46): Show |
intron_variant | MODIFIER | c.278-10379G>A | FMR1NB | ENSG00000176988.9 | transcript | ENST00000370467.8 | protein_coding | 1/5 | chrX | 147992822 | |||||||
chrX:147992826 | G | T | 1 | a0002c0002t0001g0099 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.278-10375G>T | FMR1NB | ENSG00000176988.9 | transcript | ENST00000370467.8 | protein_coding | 1/5 | chrX | 147992826 | |||||||
chrX:147992909 | C | T | 7 | a0001c0001t0001g0003 a0001c0001t0001g0046 a0001c0001t0001g0058 others(4): Show |
12 | HG00544.hp2 HG00609.hp1 HG01099.hp1 others(9): Show |
intron_variant | MODIFIER | c.278-10292C>T | FMR1NB | ENSG00000176988.9 | transcript | ENST00000370467.8 | protein_coding | 1/5 | chrX | 147992909 | |||||||
chrX:147992914 | A | G | 11 | a0002c0002t0001g0097 a0002c0002t0001g0098 a0002c0002t0001g0099 others(8): Show |
11 | HG01168.hp1 HG02258.hp1 HG02451.hp1 others(8): Show |
intron_variant | MODIFIER | c.278-10287A>G | FMR1NB | ENSG00000176988.9 | transcript | ENST00000370467.8 | protein_coding | 1/5 | chrX | 147992914 | |||||||
chrX:147992928 | C | G | 1 | a0002c0002t0001g0054 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.278-10273C>G | FMR1NB | ENSG00000176988.9 | transcript | ENST00000370467.8 | protein_coding | 1/5 | chrX | 147992928 | |||||||
chrX:147992932 | G | A | 40 | a0001c0001t0001g0004 a0001c0001t0001g0012 a0001c0001t0001g0034 others(37): Show |
49 | HG00639.hp1 HG01168.hp1 HG01243.hp1 others(46): Show |
intron_variant | MODIFIER | c.278-10269G>A | FMR1NB | ENSG00000176988.9 | transcript | ENST00000370467.8 | protein_coding | 1/5 | chrX | 147992932 | |||||||
chrX:147993009 | C | T | 9 | a0002c0002t0001g0008 a0002c0002t0001g0017 a0002c0002t0001g0048 others(6): Show |
12 | HG02615.hp1 HG02723.hp2 HG02886.hp1 others(9): Show |
intron_variant | MODIFIER | c.278-10192C>T | FMR1NB | ENSG00000176988.9 | transcript | ENST00000370467.8 | protein_coding | 1/5 | chrX | 147993009 | |||||||
chrX:147993017 | C | T | 3 | a0001c0001t0001g0195 a0001c0001t0001g0201 a0002c0002t0001g0197 |
3 | HG02809.hp2 HG03041.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.278-10184C>T | FMR1NB | ENSG00000176988.9 | transcript | ENST00000370467.8 | protein_coding | 1/5 | chrX | 147993017 | |||||||
chrX:147993018 | G | A | 4 | a0002c0002t0001g0093 a0002c0002t0001g0111 a0002c0002t0001g0112 others(1): Show |
4 | HG02257.hp1 HG02965.hp1 HG02976.hp1 others(1): Show |
intron_variant | MODIFIER | c.278-10183G>A | FMR1NB | ENSG00000176988.9 | transcript | ENST00000370467.8 | protein_coding | 1/5 | chrX | 147993018 | |||||||
chrX:147993154 | T | C | 11 | a0002c0002t0001g0097 a0002c0002t0001g0098 a0002c0002t0001g0099 others(8): Show |
11 | HG01168.hp1 HG02258.hp1 HG02451.hp1 others(8): Show |
intron_variant | MODIFIER | c.278-10047T>C | FMR1NB | ENSG00000176988.9 | transcript | ENST00000370467.8 | protein_coding | 1/5 | chrX | 147993154 | |||||||
chrX:147993265 | G | A | 1 | a0002c0002t0001g0133 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.278-9936G>A | FMR1NB | ENSG00000176988.9 | transcript | ENST00000370467.8 | protein_coding | 1/5 | chrX | 147993265 | |||||||
chrX:147993288 | C | T | 2 | a0002c0002t0001g0039 a0002c0002t0001g0116 |
2 | HG03453.hp1 NA20752.hp1 |
intron_variant | MODIFIER | c.278-9913C>T | FMR1NB | ENSG00000176988.9 | transcript | ENST00000370467.8 | protein_coding | 1/5 | chrX | 147993288 | |||||||
chrX:147993289 | G | A | 1 | a0001c0001t0001g0190 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.278-9912G>A | FMR1NB | ENSG00000176988.9 | transcript | ENST00000370467.8 | protein_coding | 1/5 | chrX | 147993289 | |||||||
chrX:147993302 | A | G | 40 | a0001c0001t0001g0004 a0001c0001t0001g0012 a0001c0001t0001g0034 others(37): Show |
49 | HG00639.hp1 HG01168.hp1 HG01243.hp1 others(46): Show |
intron_variant | MODIFIER | c.278-9899A>G | FMR1NB | ENSG00000176988.9 | transcript | ENST00000370467.8 | protein_coding | 1/5 | chrX | 147993302 | |||||||
chrX:147993381 | G | T | 1 | a0001c0001t0001g0195 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.278-9820G>T | FMR1NB | ENSG00000176988.9 | transcript | ENST00000370467.8 | protein_coding | 1/5 | chrX | 147993381 | |||||||
chrX:147993395 | G | GGGGAGA | 78 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(75): Show |
109 | HG00323.hp1 HG00408.hp1 HG00438.hp2 others(106): Show |
intron_variant | MODIFIER | c.278-9790_278-9785d others(8): Show |
FMR1NB | ENSG00000176988.9 | transcript | ENST00000370467.8 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chrX | 147993395 | ||||||
chrX:147993395 | G | GGGGAGAG others(5): Show |
40 | a0001c0001t0001g0004 a0001c0001t0001g0012 a0001c0001t0001g0034 others(37): Show |
49 | HG00639.hp1 HG01168.hp1 HG01243.hp1 others(46): Show |
intron_variant | MODIFIER | c.278-9796_278-9785d others(14): Show |
FMR1NB | ENSG00000176988.9 | transcript | ENST00000370467.8 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chrX | 147993395 | ||||||
chrX:147993523 | G | T | 1 | a0002c0002t0001g0169 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.278-9678G>T | FMR1NB | ENSG00000176988.9 | transcript | ENST00000370467.8 | protein_coding | 1/5 | chrX | 147993523 | |||||||
chrX:147993838 | C | G | 1 | a0002c0002t0001g0152 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.278-9363C>G | FMR1NB | ENSG00000176988.9 | transcript | ENST00000370467.8 | protein_coding | 1/5 | chrX | 147993838 | |||||||
chrX:147993945 | CT | C | 35 | a0001c0001t0001g0004 a0001c0001t0001g0047 a0001c0001t0001g0094 others(32): Show |
42 | HG00639.hp1 HG01168.hp1 HG01243.hp1 others(39): Show |
intron_variant | MODIFIER | c.278-9252delT | FMR1NB | ENSG00000176988.9 | transcript | ENST00000370467.8 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chrX | 147993945 | ||||||
chrX:147994088 | A | G | 2 | a0002c0002t0001g0017 a0002c0002t0001g0052 |
3 | HG03041.hp1 HG03209.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.278-9113A>G | FMR1NB | ENSG00000176988.9 | transcript | ENST00000370467.8 | protein_coding | 1/5 | chrX | 147994088 | |||||||
chrX:147994251 | G | C | 1 | a0001c0001t0001g0078 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.278-8950G>C | FMR1NB | ENSG00000176988.9 | transcript | ENST00000370467.8 | protein_coding | 1/5 | chrX | 147994251 | |||||||
chrX:147994781 | G | A | 1 | a0001c0001t0001g0064 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.278-8420G>A | FMR1NB | ENSG00000176988.9 | transcript | ENST00000370467.8 | protein_coding | 1/5 | chrX | 147994781 | |||||||
chrX:147994958 | T | G | 3 | a0002c0002t0001g0031 a0002c0002t0001g0032 a0002c0002t0001g0033 |
3 | HG01934.hp1 HG02273.hp2 HG02630.hp1 |
intron_variant | MODIFIER | c.278-8243T>G | FMR1NB | ENSG00000176988.9 | transcript | ENST00000370467.8 | protein_coding | 1/5 | chrX | 147994958 | |||||||
chrX:147994987 | A | C | 1 | a0002c0002t0001g0121 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.278-8214A>C | FMR1NB | ENSG00000176988.9 | transcript | ENST00000370467.8 | protein_coding | 1/5 | chrX | 147994987 | |||||||
chrX:147995073 | C | T | 22 | a0001c0001t0001g0005 a0001c0001t0001g0027 a0001c0001t0001g0028 others(19): Show |
29 | HG01168.hp2 HG01169.hp1 HG02080.hp1 others(26): Show |
intron_variant | MODIFIER | c.278-8128C>T | FMR1NB | ENSG00000176988.9 | transcript | ENST00000370467.8 | protein_coding | 1/5 | chrX | 147995073 | |||||||
chrX:147995144 | C | T | 5 | a0001c0001t0001g0012 a0001c0001t0001g0034 a0001c0001t0001g0108 others(2): Show |
7 | HG02486.hp1 HG02559.hp2 HG02970.hp2 others(4): Show |
intron_variant | MODIFIER | c.278-8057C>T | FMR1NB | ENSG00000176988.9 | transcript | ENST00000370467.8 | protein_coding | 1/5 | chrX | 147995144 | |||||||
chrX:147995253 | G | A | 117 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(114): Show |
157 | HG00323.hp1 HG00408.hp1 HG00438.hp2 others(154): Show |
intron_variant | MODIFIER | c.278-7948G>A | FMR1NB | ENSG00000176988.9 | transcript | ENST00000370467.8 | protein_coding | 1/5 | chrX | 147995253 | |||||||
chrX:147995310 | A | G | 40 | a0001c0001t0001g0004 a0001c0001t0001g0012 a0001c0001t0001g0034 others(37): Show |
49 | HG00639.hp1 HG01168.hp1 HG01243.hp1 others(46): Show |
intron_variant | MODIFIER | c.278-7891A>G | FMR1NB | ENSG00000176988.9 | transcript | ENST00000370467.8 | protein_coding | 1/5 | chrX | 147995310 | |||||||
chrX:147995523 | G | A | 5 | a0001c0001t0001g0012 a0001c0001t0001g0034 a0001c0001t0001g0108 others(2): Show |
7 | HG02486.hp1 HG02559.hp2 HG02970.hp2 others(4): Show |
intron_variant | MODIFIER | c.278-7678G>A | FMR1NB | ENSG00000176988.9 | transcript | ENST00000370467.8 | protein_coding | 1/5 | chrX | 147995523 | |||||||
chrX:147995800 | G | A | 40 | a0001c0001t0001g0004 a0001c0001t0001g0012 a0001c0001t0001g0034 others(37): Show |
49 | HG00639.hp1 HG01168.hp1 HG01243.hp1 others(46): Show |
intron_variant | MODIFIER | c.278-7401G>A | FMR1NB | ENSG00000176988.9 | transcript | ENST00000370467.8 | protein_coding | 1/5 | chrX | 147995800 | |||||||
chrX:147995903 | G | A | 40 | a0001c0001t0001g0004 a0001c0001t0001g0012 a0001c0001t0001g0034 others(37): Show |
49 | HG00639.hp1 HG01168.hp1 HG01243.hp1 others(46): Show |
intron_variant | MODIFIER | c.278-7298G>A | FMR1NB | ENSG00000176988.9 | transcript | ENST00000370467.8 | protein_coding | 1/5 | chrX | 147995903 | |||||||
chrX:147996169 | T | G | 1 | a0001c0001t0001g0094 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.278-7032T>G | FMR1NB | ENSG00000176988.9 | transcript | ENST00000370467.8 | protein_coding | 1/5 | chrX | 147996169 | |||||||
chrX:147996238 | G | A | 40 | a0001c0001t0001g0004 a0001c0001t0001g0012 a0001c0001t0001g0034 others(37): Show |
49 | HG00639.hp1 HG01168.hp1 HG01243.hp1 others(46): Show |
intron_variant | MODIFIER | c.278-6963G>A | FMR1NB | ENSG00000176988.9 | transcript | ENST00000370467.8 | protein_coding | 1/5 | chrX | 147996238 | |||||||
chrX:147996270 | G | T | 4 | a0002c0002t0001g0007 a0002c0002t0001g0157 a0002c0002t0001g0168 others(1): Show |
7 | HG00673.hp1 HG02040.hp1 HG02071.hp1 others(4): Show |
intron_variant | MODIFIER | c.278-6931G>T | FMR1NB | ENSG00000176988.9 | transcript | ENST00000370467.8 | protein_coding | 1/5 | chrX | 147996270 | |||||||
chrX:147996440 | A | G | 1 | a0002c0002t0001g0153 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.278-6761A>G | FMR1NB | ENSG00000176988.9 | transcript | ENST00000370467.8 | protein_coding | 1/5 | chrX | 147996440 | |||||||
chrX:147996538 | T | A | 5 | a0001c0001t0001g0012 a0001c0001t0001g0034 a0001c0001t0001g0108 others(2): Show |
7 | HG02486.hp1 HG02559.hp2 HG02970.hp2 others(4): Show |
intron_variant | MODIFIER | c.278-6663T>A | FMR1NB | ENSG00000176988.9 | transcript | ENST00000370467.8 | protein_coding | 1/5 | chrX | 147996538 | |||||||
chrX:147996782 | C | T | 1 | a0002c0002t0001g0053 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.278-6419C>T | FMR1NB | ENSG00000176988.9 | transcript | ENST00000370467.8 | protein_coding | 1/5 | chrX | 147996782 | |||||||
chrX:147996866 | A | G | 3 | a0001c0001t0001g0029 a0001c0001t0001g0085 a0001c0001t0001g0086 |
3 | HG01074.hp1 HG01261.hp1 HG01975.hp2 |
intron_variant | MODIFIER | c.278-6335A>G | FMR1NB | ENSG00000176988.9 | transcript | ENST00000370467.8 | protein_coding | 1/5 | chrX | 147996866 | |||||||
chrX:147996869 | C | T | 1 | a0002c0002t0001g0050 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.278-6332C>T | FMR1NB | ENSG00000176988.9 | transcript | ENST00000370467.8 | protein_coding | 1/5 | chrX | 147996869 | |||||||
chrX:147997058 | G | T | 4 | a0002c0002t0001g0196 a0002c0002t0001g0206 a0002c0002t0001g0207 others(1): Show |
4 | HG02630.hp2 HG02818.hp2 HG02896.hp1 others(1): Show |
intron_variant | MODIFIER | c.278-6143G>T | FMR1NB | ENSG00000176988.9 | transcript | ENST00000370467.8 | protein_coding | 1/5 | chrX | 147997058 | |||||||
chrX:147997657 | C | T | 40 | a0001c0001t0001g0004 a0001c0001t0001g0012 a0001c0001t0001g0034 others(37): Show |
49 | HG00639.hp1 HG01168.hp1 HG01243.hp1 others(46): Show |
intron_variant | MODIFIER | c.278-5544C>T | FMR1NB | ENSG00000176988.9 | transcript | ENST00000370467.8 | protein_coding | 1/5 | chrX | 147997657 | |||||||
chrX:147997764 | G | GA | 5 | a0001c0001t0001g0012 a0001c0001t0001g0034 a0001c0001t0001g0108 others(2): Show |
7 | HG02486.hp1 HG02559.hp2 HG02970.hp2 others(4): Show |
intron_variant | MODIFIER | c.278-5428dupA | FMR1NB | ENSG00000176988.9 | transcript | ENST00000370467.8 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chrX | 147997764 | ||||||
chrX:147997793 | G | A | 15 | a0001c0001t0001g0005 a0001c0001t0001g0027 a0001c0001t0001g0028 others(12): Show |
22 | HG01168.hp2 HG01169.hp1 HG02080.hp1 others(19): Show |
intron_variant | MODIFIER | c.278-5408G>A | FMR1NB | ENSG00000176988.9 | transcript | ENST00000370467.8 | protein_coding | 1/5 | chrX | 147997793 | |||||||
chrX:147997835 | CAA | C | 5 | a0001c0001t0001g0004 a0001c0001t0001g0047 a0001c0001t0001g0094 others(2): Show |
9 | HG00639.hp1 HG01891.hp1 HG02280.hp2 others(6): Show |
intron_variant | MODIFIER | c.278-5361_278-5360d others(4): Show |
FMR1NB | ENSG00000176988.9 | transcript | ENST00000370467.8 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chrX | 147997835 | ||||||
chrX:147997841 | A | T | 5 | a0001c0001t0001g0004 a0001c0001t0001g0047 a0001c0001t0001g0094 others(2): Show |
9 | HG00639.hp1 HG01891.hp1 HG02280.hp2 others(6): Show |
intron_variant | MODIFIER | c.278-5360A>T | FMR1NB | ENSG00000176988.9 | transcript | ENST00000370467.8 | protein_coding | 1/5 | chrX | 147997841 | |||||||
chrX:147997852 | A | G | 56 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0006 others(53): Show |
80 | HG00323.hp1 HG00408.hp1 HG00438.hp2 others(77): Show |
intron_variant | MODIFIER | c.278-5349A>G | FMR1NB | ENSG00000176988.9 | transcript | ENST00000370467.8 | protein_coding | 1/5 | chrX | 147997852 | |||||||
chrX:147997855 | A | G | 56 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0006 others(53): Show |
80 | HG00323.hp1 HG00408.hp1 HG00438.hp2 others(77): Show |
intron_variant | MODIFIER | c.278-5346A>G | FMR1NB | ENSG00000176988.9 | transcript | ENST00000370467.8 | protein_coding | 1/5 | chrX | 147997855 | |||||||
chrX:147997915 | C | T | 4 | a0002c0002t0001g0116 a0002c0002t0001g0150 a0002c0002t0001g0151 others(1): Show |
4 | HG01081.hp1 HG01106.hp1 HG01346.hp2 others(1): Show |
intron_variant | MODIFIER | c.278-5286C>T | FMR1NB | ENSG00000176988.9 | transcript | ENST00000370467.8 | protein_coding | 1/5 | chrX | 147997915 | |||||||
chrX:147997916 | G | A | 1 | a0002c0002t0001g0093 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.278-5285G>A | FMR1NB | ENSG00000176988.9 | transcript | ENST00000370467.8 | protein_coding | 1/5 | chrX | 147997916 | |||||||
chrX:147997962 | T | C | 1 | a0001c0001t0001g0184 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.278-5239T>C | FMR1NB | ENSG00000176988.9 | transcript | ENST00000370467.8 | protein_coding | 1/5 | chrX | 147997962 | |||||||
chrX:147997976 | A | G | 2 | a0001c0001t0001g0201 a0002c0002t0001g0197 |
2 | HG02809.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.278-5225A>G | FMR1NB | ENSG00000176988.9 | transcript | ENST00000370467.8 | protein_coding | 1/5 | chrX | 147997976 | |||||||
chrX:147998058 | T | G | 40 | a0001c0001t0001g0004 a0001c0001t0001g0012 a0001c0001t0001g0034 others(37): Show |
49 | HG00639.hp1 HG01168.hp1 HG01243.hp1 others(46): Show |
intron_variant | MODIFIER | c.278-5143T>G | FMR1NB | ENSG00000176988.9 | transcript | ENST00000370467.8 | protein_coding | 1/5 | chrX | 147998058 | |||||||
chrX:147998240 | A | G | 1 | a0002c0002t0001g0050 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.278-4961A>G | FMR1NB | ENSG00000176988.9 | transcript | ENST00000370467.8 | protein_coding | 1/5 | chrX | 147998240 | |||||||
chrX:147998244 | C | G | 23 | a0001c0001t0001g0005 a0001c0001t0001g0027 a0001c0001t0001g0028 others(20): Show |
30 | HG01168.hp2 HG01169.hp1 HG02080.hp1 others(27): Show |
intron_variant | MODIFIER | c.278-4957C>G | FMR1NB | ENSG00000176988.9 | transcript | ENST00000370467.8 | protein_coding | 1/5 | chrX | 147998244 | |||||||
chrX:147998345 | A | G | 1 | a0002c0002t0001g0039 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.278-4856A>G | FMR1NB | ENSG00000176988.9 | transcript | ENST00000370467.8 | protein_coding | 1/5 | chrX | 147998345 | |||||||
chrX:147998390 | TG | T | 40 | a0001c0001t0001g0004 a0001c0001t0001g0012 a0001c0001t0001g0034 others(37): Show |
49 | HG00639.hp1 HG01168.hp1 HG01243.hp1 others(46): Show |
intron_variant | MODIFIER | c.278-4808delG | FMR1NB | ENSG00000176988.9 | transcript | ENST00000370467.8 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chrX | 147998390 | ||||||
chrX:147998542 | A | G | 1 | a0002c0002t0001g0153 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.278-4659A>G | FMR1NB | ENSG00000176988.9 | transcript | ENST00000370467.8 | protein_coding | 1/5 | chrX | 147998542 | |||||||
chrX:147998552 | A | G | 1 | a0002c0002t0001g0118 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.278-4649A>G | FMR1NB | ENSG00000176988.9 | transcript | ENST00000370467.8 | protein_coding | 1/5 | chrX | 147998552 | |||||||
chrX:147998618 | A | G | 2 | a0001c0001t0001g0190 a0001c0001t0001g0191 |
2 | HG01891.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.278-4583A>G | FMR1NB | ENSG00000176988.9 | transcript | ENST00000370467.8 | protein_coding | 1/5 | chrX | 147998618 | |||||||
chrX:147998631 | C | A | 40 | a0001c0001t0001g0004 a0001c0001t0001g0012 a0001c0001t0001g0034 others(37): Show |
49 | HG00639.hp1 HG01168.hp1 HG01243.hp1 others(46): Show |
intron_variant | MODIFIER | c.278-4570C>A | FMR1NB | ENSG00000176988.9 | transcript | ENST00000370467.8 | protein_coding | 1/5 | chrX | 147998631 | |||||||
chrX:147998651 | C | T | 3 | a0001c0001t0001g0011 a0001c0001t0001g0056 a0001c0001t0001g0076 |
5 | NA18961.hp1 NA18966.hp1 NA18992.hp2 others(2): Show |
intron_variant | MODIFIER | c.278-4550C>T | FMR1NB | ENSG00000176988.9 | transcript | ENST00000370467.8 | protein_coding | 1/5 | chrX | 147998651 | |||||||
chrX:147998764 | A | G | 35 | a0001c0001t0001g0004 a0001c0001t0001g0047 a0001c0001t0001g0094 others(32): Show |
42 | HG00639.hp1 HG01168.hp1 HG01243.hp1 others(39): Show |
intron_variant | MODIFIER | c.278-4437A>G | FMR1NB | ENSG00000176988.9 | transcript | ENST00000370467.8 | protein_coding | 1/5 | chrX | 147998764 | |||||||
chrX:147999064 | A | G | 1 | a0001c0001t0001g0205 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.278-4137A>G | FMR1NB | ENSG00000176988.9 | transcript | ENST00000370467.8 | protein_coding | 1/5 | chrX | 147999064 | |||||||
chrX:147999077 | G | A | 1 | a0001c0001t0001g0042 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.278-4124G>A | FMR1NB | ENSG00000176988.9 | transcript | ENST00000370467.8 | protein_coding | 1/5 | chrX | 147999077 | |||||||
chrX:147999533 | C | A | 1 | a0001c0001t0001g0191 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.278-3668C>A | FMR1NB | ENSG00000176988.9 | transcript | ENST00000370467.8 | protein_coding | 1/5 | chrX | 147999533 | |||||||
chrX:147999533 | C | CCT | 35 | a0001c0001t0001g0004 a0001c0001t0001g0047 a0001c0001t0001g0094 others(32): Show |
42 | HG00639.hp1 HG01168.hp1 HG01243.hp1 others(39): Show |
intron_variant | MODIFIER | c.278-3668_278-3667i others(4): Show |
FMR1NB | ENSG00000176988.9 | transcript | ENST00000370467.8 | protein_coding | 1/5 | chrX | 147999533 | |||||||
chrX:147999533 | C | CCTT | 5 | a0001c0001t0001g0012 a0001c0001t0001g0034 a0001c0001t0001g0108 others(2): Show |
7 | HG02486.hp1 HG02559.hp2 HG02970.hp2 others(4): Show |
intron_variant | MODIFIER | c.278-3668_278-3667i others(5): Show |
FMR1NB | ENSG00000176988.9 | transcript | ENST00000370467.8 | protein_coding | 1/5 | chrX | 147999533 | |||||||
chrX:147999533 | C | CT | 76 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(73): Show |
107 | HG00323.hp1 HG00408.hp1 HG00438.hp2 others(104): Show |
intron_variant | MODIFIER | c.278-3656dupT | FMR1NB | ENSG00000176988.9 | transcript | ENST00000370467.8 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chrX | 147999533 | ||||||
chrX:147999863 | A | G | 5 | a0001c0001t0001g0012 a0001c0001t0001g0034 a0001c0001t0001g0108 others(2): Show |
7 | HG02486.hp1 HG02559.hp2 HG02970.hp2 others(4): Show |
intron_variant | MODIFIER | c.278-3338A>G | FMR1NB | ENSG00000176988.9 | transcript | ENST00000370467.8 | protein_coding | 1/5 | chrX | 147999863 | |||||||
chrX:147999886 | A | G | 1 | a0002c0002t0001g0054 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.278-3315A>G | FMR1NB | ENSG00000176988.9 | transcript | ENST00000370467.8 | protein_coding | 1/5 | chrX | 147999886 | |||||||
chrX:147999931 | C | T | 1 | a0001c0001t0001g0183 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.278-3270C>T | FMR1NB | ENSG00000176988.9 | transcript | ENST00000370467.8 | protein_coding | 1/5 | chrX | 147999931 | |||||||
chrX:147999961 | T | G | 1 | a0002c0002t0001g0141 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.278-3240T>G | FMR1NB | ENSG00000176988.9 | transcript | ENST00000370467.8 | protein_coding | 1/5 | chrX | 147999961 | |||||||
chrX:148000507 | A | G | 2 | a0002c0002t0001g0106 a0002c0002t0001g0107 |
2 | HG03017.hp1 HG03491.hp1 |
intron_variant | MODIFIER | c.278-2694A>G | FMR1NB | ENSG00000176988.9 | transcript | ENST00000370467.8 | protein_coding | 1/5 | chrX | 148000507 | |||||||
chrX:148000563 | G | A | 5 | a0001c0001t0001g0004 a0001c0001t0001g0047 a0001c0001t0001g0094 others(2): Show |
9 | HG00639.hp1 HG01891.hp1 HG02280.hp2 others(6): Show |
intron_variant | MODIFIER | c.278-2638G>A | FMR1NB | ENSG00000176988.9 | transcript | ENST00000370467.8 | protein_coding | 1/5 | chrX | 148000563 | |||||||
chrX:148000578 | A | G | 1 | a0002c0002t0001g0175 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.278-2623A>G | FMR1NB | ENSG00000176988.9 | transcript | ENST00000370467.8 | protein_coding | 1/5 | chrX | 148000578 | |||||||
chrX:148000789 | T | C | 138 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(135): Show |
186 | HG00323.hp1 HG00408.hp1 HG00438.hp2 others(183): Show |
intron_variant | MODIFIER | c.278-2412T>C | FMR1NB | ENSG00000176988.9 | transcript | ENST00000370467.8 | protein_coding | 1/5 | chrX | 148000789 | |||||||
chrX:148001261 | A | G | 1 | a0002c0002t0001g0151 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.278-1940A>G | FMR1NB | ENSG00000176988.9 | transcript | ENST00000370467.8 | protein_coding | 1/5 | chrX | 148001261 | |||||||
chrX:148001357 | A | G | 1 | a0002c0002t0001g0208 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.278-1844A>G | FMR1NB | ENSG00000176988.9 | transcript | ENST00000370467.8 | protein_coding | 1/5 | chrX | 148001357 | |||||||
chrX:148001557 | C | T | 1 | a0002c0002t0001g0161 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.278-1644C>T | FMR1NB | ENSG00000176988.9 | transcript | ENST00000370467.8 | protein_coding | 1/5 | chrX | 148001557 | |||||||
chrX:148001560 | G | C | 1 | a0002c0002t0001g0100 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.278-1641G>C | FMR1NB | ENSG00000176988.9 | transcript | ENST00000370467.8 | protein_coding | 1/5 | chrX | 148001560 | |||||||
chrX:148001682 | G | A | 1 | a0001c0001t0001g0066 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.278-1519G>A | FMR1NB | ENSG00000176988.9 | transcript | ENST00000370467.8 | protein_coding | 1/5 | chrX | 148001682 | |||||||
chrX:148001807 | T | C | 1 | a0001c0001t0001g0184 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.278-1394T>C | FMR1NB | ENSG00000176988.9 | transcript | ENST00000370467.8 | protein_coding | 1/5 | chrX | 148001807 | |||||||
chrX:148001857 | ATAAGGAT others(4): Show |
A | 1 | a0002c0002t0001g0036 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.278-1336_278-1326d others(13): Show |
FMR1NB | ENSG00000176988.9 | transcript | ENST00000370467.8 | protein_coding | 1/5 | INFO_REALIGN_3_PRIME | chrX | 148001857 | ||||||
chrX:148001952 | A | G | 3 | a0001c0001t0002g0193 a0002c0002t0001g0181 a0002c0002t0001g0182 |
3 | HG03225.hp1 NA18906.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.278-1249A>G | FMR1NB | ENSG00000176988.9 | transcript | ENST00000370467.8 | protein_coding | 1/5 | chrX | 148001952 | |||||||
chrX:148002134 | C | T | 5 | a0001c0001t0001g0012 a0001c0001t0001g0034 a0001c0001t0001g0108 others(2): Show |
7 | HG02486.hp1 HG02559.hp2 HG02970.hp2 others(4): Show |
intron_variant | MODIFIER | c.278-1067C>T | FMR1NB | ENSG00000176988.9 | transcript | ENST00000370467.8 | protein_coding | 1/5 | chrX | 148002134 | |||||||
chrX:148002253 | C | T | 1 | a0002c0002t0001g0166 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.278-948C>T | FMR1NB | ENSG00000176988.9 | transcript | ENST00000370467.8 | protein_coding | 1/5 | chrX | 148002253 | |||||||
chrX:148002280 | A | G | 1 | a0002c0002t0001g0133 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.278-921A>G | FMR1NB | ENSG00000176988.9 | transcript | ENST00000370467.8 | protein_coding | 1/5 | chrX | 148002280 | |||||||
chrX:148002344 | A | G | 5 | a0001c0001t0001g0025 a0001c0001t0001g0026 a0001c0001t0001g0172 others(2): Show |
7 | HG01123.hp2 HG01884.hp1 HG02109.hp1 others(4): Show |
intron_variant | MODIFIER | c.278-857A>G | FMR1NB | ENSG00000176988.9 | transcript | ENST00000370467.8 | protein_coding | 1/5 | chrX | 148002344 | |||||||
chrX:148002387 | A | G | 209 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(206): Show |
271 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(268): Show |
intron_variant | MODIFIER | c.278-814A>G | FMR1NB | ENSG00000176988.9 | transcript | ENST00000370467.8 | protein_coding | 1/5 | chrX | 148002387 | |||||||
chrX:148002548 | G | A | 40 | a0001c0001t0001g0004 a0001c0001t0001g0012 a0001c0001t0001g0034 others(37): Show |
49 | HG00639.hp1 HG01168.hp1 HG01243.hp1 others(46): Show |
intron_variant | MODIFIER | c.278-653G>A | FMR1NB | ENSG00000176988.9 | transcript | ENST00000370467.8 | protein_coding | 1/5 | chrX | 148002548 | |||||||
chrX:148003152 | G | A | 5 | a0001c0001t0001g0012 a0001c0001t0001g0034 a0001c0001t0001g0108 others(2): Show |
7 | HG02486.hp1 HG02559.hp2 HG02970.hp2 others(4): Show |
intron_variant | MODIFIER | c.278-49G>A | FMR1NB | ENSG00000176988.9 | transcript | ENST00000370467.8 | protein_coding | 1/5 | chrX | 148003152 | |||||||
chrX:148003628 | G | A | 112 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(109): Show |
148 | HG00323.hp1 HG00408.hp1 HG00438.hp2 others(145): Show |
intron_variant | MODIFIER | c.397+308G>A | FMR1NB | ENSG00000176988.9 | transcript | ENST00000370467.8 | protein_coding | 2/5 | chrX | 148003628 | |||||||
chrX:148003722 | T | C | 1 | a0002c0002t0001g0142 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.397+402T>C | FMR1NB | ENSG00000176988.9 | transcript | ENST00000370467.8 | protein_coding | 2/5 | chrX | 148003722 | |||||||
chrX:148003944 | A | T | 55 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0006 others(52): Show |
79 | HG00323.hp1 HG00408.hp1 HG00438.hp2 others(76): Show |
intron_variant | MODIFIER | c.397+624A>T | FMR1NB | ENSG00000176988.9 | transcript | ENST00000370467.8 | protein_coding | 2/5 | chrX | 148003944 | |||||||
chrX:148003952 | T | G | 2 | a0001c0001t0001g0012 a0001c0001t0001g0108 |
4 | HG02559.hp2 HG02970.hp2 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.397+632T>G | FMR1NB | ENSG00000176988.9 | transcript | ENST00000370467.8 | protein_coding | 2/5 | chrX | 148003952 | |||||||
chrX:148004099 | A | G | 35 | a0001c0001t0001g0012 a0001c0001t0001g0034 a0001c0001t0001g0108 others(32): Show |
40 | HG01168.hp1 HG01243.hp1 HG02257.hp1 others(37): Show |
intron_variant | MODIFIER | c.397+779A>G | FMR1NB | ENSG00000176988.9 | transcript | ENST00000370467.8 | protein_coding | 2/5 | chrX | 148004099 | |||||||
chrX:148004208 | C | T | 1 | a0002c0002t0001g0177 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.397+888C>T | FMR1NB | ENSG00000176988.9 | transcript | ENST00000370467.8 | protein_coding | 2/5 | chrX | 148004208 | |||||||
chrX:148004219 | C | T | 5 | a0001c0001t0001g0012 a0001c0001t0001g0034 a0001c0001t0001g0108 others(2): Show |
7 | HG02486.hp1 HG02559.hp2 HG02970.hp2 others(4): Show |
intron_variant | MODIFIER | c.397+899C>T | FMR1NB | ENSG00000176988.9 | transcript | ENST00000370467.8 | protein_coding | 2/5 | chrX | 148004219 | |||||||
chrX:148004337 | A | G | 1 | a0002c0002t0001g0149 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.397+1017A>G | FMR1NB | ENSG00000176988.9 | transcript | ENST00000370467.8 | protein_coding | 2/5 | chrX | 148004337 | |||||||
chrX:148004392 | T | C | 2 | a0002c0002t0001g0035 a0002c0002t0001g0037 |
2 | HG01243.hp1 HG02647.hp1 |
intron_variant | MODIFIER | c.397+1072T>C | FMR1NB | ENSG00000176988.9 | transcript | ENST00000370467.8 | protein_coding | 2/5 | chrX | 148004392 | |||||||
chrX:148004403 | C | A | 2 | a0002c0002t0001g0093 a0002c0002t0001g0181 |
2 | HG02257.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.397+1083C>A | FMR1NB | ENSG00000176988.9 | transcript | ENST00000370467.8 | protein_coding | 2/5 | chrX | 148004403 | |||||||
chrX:148004477 | A | T | 22 | a0001c0001t0001g0005 a0001c0001t0001g0027 a0001c0001t0001g0028 others(19): Show |
29 | HG01168.hp2 HG01169.hp1 HG02080.hp1 others(26): Show |
intron_variant | MODIFIER | c.397+1157A>T | FMR1NB | ENSG00000176988.9 | transcript | ENST00000370467.8 | protein_coding | 2/5 | chrX | 148004477 | |||||||
chrX:148004495 | A | C | 1 | a0002c0002t0001g0148 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.397+1175A>C | FMR1NB | ENSG00000176988.9 | transcript | ENST00000370467.8 | protein_coding | 2/5 | chrX | 148004495 | |||||||
chrX:148004519 | A | G | 35 | a0001c0001t0001g0012 a0001c0001t0001g0034 a0001c0001t0001g0108 others(32): Show |
40 | HG01168.hp1 HG01243.hp1 HG02257.hp1 others(37): Show |
intron_variant | MODIFIER | c.397+1199A>G | FMR1NB | ENSG00000176988.9 | transcript | ENST00000370467.8 | protein_coding | 2/5 | chrX | 148004519 | |||||||
chrX:148004679 | G | T | 1 | a0001c0001t0001g0078 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.397+1359G>T | FMR1NB | ENSG00000176988.9 | transcript | ENST00000370467.8 | protein_coding | 2/5 | chrX | 148004679 | |||||||
chrX:148004927 | G | A | 1 | a0002c0002t0001g0118 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.397+1607G>A | FMR1NB | ENSG00000176988.9 | transcript | ENST00000370467.8 | protein_coding | 2/5 | chrX | 148004927 | |||||||
chrX:148004963 | C | A | 5 | a0001c0001t0001g0012 a0001c0001t0001g0034 a0001c0001t0001g0108 others(2): Show |
7 | HG02486.hp1 HG02559.hp2 HG02970.hp2 others(4): Show |
intron_variant | MODIFIER | c.397+1643C>A | FMR1NB | ENSG00000176988.9 | transcript | ENST00000370467.8 | protein_coding | 2/5 | chrX | 148004963 | |||||||
chrX:148005103 | C | T | 2 | a0001c0001t0001g0020 a0001c0001t0001g0045 |
3 | HG03491.hp2 HG03492.hp1 HG03688.hp1 |
intron_variant | MODIFIER | c.398-1599C>T | FMR1NB | ENSG00000176988.9 | transcript | ENST00000370467.8 | protein_coding | 2/5 | chrX | 148005103 | |||||||
chrX:148005447 | T | C | 1 | a0002c0002t0001g0175 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.398-1255T>C | FMR1NB | ENSG00000176988.9 | transcript | ENST00000370467.8 | protein_coding | 2/5 | chrX | 148005447 | |||||||
chrX:148005663 | A | G | 1 | a0002c0002t0001g0174 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.398-1039A>G | FMR1NB | ENSG00000176988.9 | transcript | ENST00000370467.8 | protein_coding | 2/5 | chrX | 148005663 | |||||||
chrX:148005669 | G | A | 10 | a0002c0002t0001g0008 a0002c0002t0001g0017 a0002c0002t0001g0048 others(7): Show |
13 | HG02615.hp1 HG02723.hp2 HG02886.hp1 others(10): Show |
intron_variant | MODIFIER | c.398-1033G>A | FMR1NB | ENSG00000176988.9 | transcript | ENST00000370467.8 | protein_coding | 2/5 | chrX | 148005669 | |||||||
chrX:148005746 | T | C | 5 | a0001c0001t0001g0012 a0001c0001t0001g0034 a0001c0001t0001g0108 others(2): Show |
7 | HG02486.hp1 HG02559.hp2 HG02970.hp2 others(4): Show |
intron_variant | MODIFIER | c.398-956T>C | FMR1NB | ENSG00000176988.9 | transcript | ENST00000370467.8 | protein_coding | 2/5 | chrX | 148005746 | |||||||
chrX:148005921 | G | A | 1 | a0002c0002t0001g0208 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.398-781G>A | FMR1NB | ENSG00000176988.9 | transcript | ENST00000370467.8 | protein_coding | 2/5 | chrX | 148005921 | |||||||
chrX:148005932 | T | C | 1 | a0002c0002t0001g0036 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.398-770T>C | FMR1NB | ENSG00000176988.9 | transcript | ENST00000370467.8 | protein_coding | 2/5 | chrX | 148005932 | |||||||
chrX:148005937 | C | T | 1 | a0002c0002t0001g0182 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.398-765C>T | FMR1NB | ENSG00000176988.9 | transcript | ENST00000370467.8 | protein_coding | 2/5 | chrX | 148005937 | |||||||
chrX:148006001 | A | G | 132 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(129): Show |
180 | HG00323.hp1 HG00408.hp1 HG00438.hp2 others(177): Show |
intron_variant | MODIFIER | c.398-701A>G | FMR1NB | ENSG00000176988.9 | transcript | ENST00000370467.8 | protein_coding | 2/5 | chrX | 148006001 | |||||||
chrX:148006012 | T | C | 5 | a0001c0001t0001g0012 a0001c0001t0001g0034 a0001c0001t0001g0108 others(2): Show |
7 | HG02486.hp1 HG02559.hp2 HG02970.hp2 others(4): Show |
intron_variant | MODIFIER | c.398-690T>C | FMR1NB | ENSG00000176988.9 | transcript | ENST00000370467.8 | protein_coding | 2/5 | chrX | 148006012 | |||||||
chrX:148006120 | T | TG | 41 | a0001c0001t0001g0012 a0001c0001t0001g0034 a0001c0001t0001g0108 others(38): Show |
46 | HG01168.hp1 HG01243.hp1 HG02257.hp1 others(43): Show |
intron_variant | MODIFIER | c.398-582_398-581ins others(1): Show |
FMR1NB | ENSG00000176988.9 | transcript | ENST00000370467.8 | protein_coding | 2/5 | chrX | 148006120 | |||||||
chrX:148006131 | T | A | 21 | a0001c0001t0001g0005 a0001c0001t0001g0020 a0001c0001t0001g0027 others(18): Show |
29 | HG00544.hp2 HG01168.hp2 HG01169.hp1 others(26): Show |
intron_variant | MODIFIER | c.398-571T>A | FMR1NB | ENSG00000176988.9 | transcript | ENST00000370467.8 | protein_coding | 2/5 | chrX | 148006131 | |||||||
chrX:148006435 | A | T | 41 | a0001c0001t0001g0012 a0001c0001t0001g0034 a0001c0001t0001g0108 others(38): Show |
46 | HG01168.hp1 HG01243.hp1 HG02257.hp1 others(43): Show |
intron_variant | MODIFIER | c.398-267A>T | FMR1NB | ENSG00000176988.9 | transcript | ENST00000370467.8 | protein_coding | 2/5 | chrX | 148006435 | |||||||
chrX:148006525 | A | G | 1 | a0001c0001t0001g0062 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.398-177A>G | FMR1NB | ENSG00000176988.9 | transcript | ENST00000370467.8 | protein_coding | 2/5 | chrX | 148006525 | |||||||
chrX:148006549 | T | A | 1 | a0001c0001t0001g0084 | 1 | NA19080.hp1 | intron_variant | MODIFIER | c.398-153T>A | FMR1NB | ENSG00000176988.9 | transcript | ENST00000370467.8 | protein_coding | 2/5 | chrX | 148006549 | |||||||
chrX:148006680 | C | T | 1 | a0001c0001t0001g0075 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.398-22C>T | FMR1NB | ENSG00000176988.9 | transcript | ENST00000370467.8 | protein_coding | 2/5 | chrX | 148006680 | |||||||
chrX:148007065 | A | G | 1 | a0001c0001t0001g0034 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.538+223A>G | FMR1NB | ENSG00000176988.9 | transcript | ENST00000370467.8 | protein_coding | 3/5 | chrX | 148007065 | |||||||
chrX:148007101 | C | A | 1 | a0002c0002t0001g0024 | 2 | HG02572.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.538+259C>A | FMR1NB | ENSG00000176988.9 | transcript | ENST00000370467.8 | protein_coding | 3/5 | chrX | 148007101 | |||||||
chrX:148007150 | G | A | 1 | a0002c0002t0001g0181 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.538+308G>A | FMR1NB | ENSG00000176988.9 | transcript | ENST00000370467.8 | protein_coding | 3/5 | chrX | 148007150 | |||||||
chrX:148007257 | T | A | 2 | a0002c0002t0001g0130 a0002c0002t0001g0143 |
2 | HG01255.hp1 HG01256.hp1 |
intron_variant | MODIFIER | c.538+415T>A | FMR1NB | ENSG00000176988.9 | transcript | ENST00000370467.8 | protein_coding | 3/5 | chrX | 148007257 | |||||||
chrX:148007402 | G | A | 1 | a0002c0002t0001g0206 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.538+560G>A | FMR1NB | ENSG00000176988.9 | transcript | ENST00000370467.8 | protein_coding | 3/5 | chrX | 148007402 | |||||||
chrX:148007481 | G | A | 1 | a0001c0001t0001g0202 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.538+639G>A | FMR1NB | ENSG00000176988.9 | transcript | ENST00000370467.8 | protein_coding | 3/5 | chrX | 148007481 | |||||||
chrX:148007864 | A | G | 1 | a0001c0001t0001g0074 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.539-754A>G | FMR1NB | ENSG00000176988.9 | transcript | ENST00000370467.8 | protein_coding | 3/5 | chrX | 148007864 | |||||||
chrX:148008204 | G | A | 1 | a0001c0001t0001g0190 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.539-414G>A | FMR1NB | ENSG00000176988.9 | transcript | ENST00000370467.8 | protein_coding | 3/5 | chrX | 148008204 | |||||||
chrX:148008336 | G | A | 1 | a0002c0002t0001g0154 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.539-282G>A | FMR1NB | ENSG00000176988.9 | transcript | ENST00000370467.8 | protein_coding | 3/5 | chrX | 148008336 | |||||||
chrX:148008417 | G | A | 6 | a0002c0002t0001g0023 a0002c0002t0001g0119 a0002c0002t0001g0131 others(3): Show |
7 | HG02109.hp2 HG02145.hp1 HG02280.hp1 others(4): Show |
intron_variant | MODIFIER | c.539-201G>A | FMR1NB | ENSG00000176988.9 | transcript | ENST00000370467.8 | protein_coding | 3/5 | chrX | 148008417 | |||||||
chrX:148008756 | G | A | 41 | a0001c0001t0001g0012 a0001c0001t0001g0034 a0001c0001t0001g0108 others(38): Show |
46 | HG01168.hp1 HG01243.hp1 HG02257.hp1 others(43): Show |
intron_variant | MODIFIER | c.632+45G>A | FMR1NB | ENSG00000176988.9 | transcript | ENST00000370467.8 | protein_coding | 4/5 | chrX | 148008756 | |||||||
chrX:148008968 | T | A | 1 | a0002c0002t0001g0124 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.632+257T>A | FMR1NB | ENSG00000176988.9 | transcript | ENST00000370467.8 | protein_coding | 4/5 | chrX | 148008968 | |||||||
chrX:148008996 | A | G | 1 | a0001c0001t0002g0193 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.632+285A>G | FMR1NB | ENSG00000176988.9 | transcript | ENST00000370467.8 | protein_coding | 4/5 | chrX | 148008996 | |||||||
chrX:148009001 | G | A | 41 | a0001c0001t0001g0012 a0001c0001t0001g0034 a0001c0001t0001g0108 others(38): Show |
46 | HG01168.hp1 HG01243.hp1 HG02257.hp1 others(43): Show |
intron_variant | MODIFIER | c.632+290G>A | FMR1NB | ENSG00000176988.9 | transcript | ENST00000370467.8 | protein_coding | 4/5 | chrX | 148009001 | |||||||
chrX:148009031 | A | G | 1 | a0001c0001t0001g0073 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.632+320A>G | FMR1NB | ENSG00000176988.9 | transcript | ENST00000370467.8 | protein_coding | 4/5 | chrX | 148009031 | |||||||
chrX:148009040 | G | A | 1 | a0001c0001t0001g0062 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.632+329G>A | FMR1NB | ENSG00000176988.9 | transcript | ENST00000370467.8 | protein_coding | 4/5 | chrX | 148009040 | |||||||
chrX:148009179 | G | A | 1 | a0001c0001t0001g0087 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.632+468G>A | FMR1NB | ENSG00000176988.9 | transcript | ENST00000370467.8 | protein_coding | 4/5 | chrX | 148009179 | |||||||
chrX:148009513 | CT | C | 11 | a0001c0001t0001g0137 a0001c0001t0002g0193 a0002c0002t0001g0008 others(8): Show |
14 | HG02615.hp1 HG02723.hp2 HG02886.hp1 others(11): Show |
intron_variant | MODIFIER | c.632+817delT | FMR1NB | ENSG00000176988.9 | transcript | ENST00000370467.8 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chrX | 148009513 | ||||||
chrX:148009651 | C | T | 1 | a0001c0001t0002g0193 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.632+940C>T | FMR1NB | ENSG00000176988.9 | transcript | ENST00000370467.8 | protein_coding | 4/5 | chrX | 148009651 | |||||||
chrX:148010101 | A | AT | 40 | a0001c0001t0001g0012 a0001c0001t0001g0034 a0001c0001t0001g0108 others(37): Show |
44 | HG01168.hp1 HG01243.hp1 HG02257.hp1 others(41): Show |
intron_variant | MODIFIER | c.632+1399dupT | FMR1NB | ENSG00000176988.9 | transcript | ENST00000370467.8 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chrX | 148010101 | ||||||
chrX:148010288 | C | T | 49 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0006 others(46): Show |
71 | HG00323.hp1 HG00408.hp1 HG00438.hp2 others(68): Show |
intron_variant | MODIFIER | c.632+1577C>T | FMR1NB | ENSG00000176988.9 | transcript | ENST00000370467.8 | protein_coding | 4/5 | chrX | 148010288 | |||||||
chrX:148010499 | A | G | 41 | a0001c0001t0001g0012 a0001c0001t0001g0034 a0001c0001t0001g0108 others(38): Show |
46 | HG01168.hp1 HG01243.hp1 HG02257.hp1 others(43): Show |
intron_variant | MODIFIER | c.632+1788A>G | FMR1NB | ENSG00000176988.9 | transcript | ENST00000370467.8 | protein_coding | 4/5 | chrX | 148010499 | |||||||
chrX:148010773 | TG | T | 3 | a0002c0002t0001g0196 a0002c0002t0001g0206 a0002c0002t0001g0207 |
3 | HG02630.hp2 HG02896.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.632+2063delG | FMR1NB | ENSG00000176988.9 | transcript | ENST00000370467.8 | protein_coding | 4/5 | chrX | 148010773 | |||||||
chrX:148010892 | G | A | 77 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0006 others(74): Show |
101 | HG00323.hp1 HG00408.hp1 HG00438.hp2 others(98): Show |
intron_variant | MODIFIER | c.632+2181G>A | FMR1NB | ENSG00000176988.9 | transcript | ENST00000370467.8 | protein_coding | 4/5 | chrX | 148010892 | |||||||
chrX:148011120 | C | T | 1 | a0001c0001t0001g0087 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.632+2409C>T | FMR1NB | ENSG00000176988.9 | transcript | ENST00000370467.8 | protein_coding | 4/5 | chrX | 148011120 | |||||||
chrX:148011198 | C | A | 36 | a0001c0001t0001g0012 a0001c0001t0001g0034 a0001c0001t0001g0108 others(33): Show |
41 | HG01168.hp1 HG01891.hp2 HG02257.hp1 others(38): Show |
intron_variant | MODIFIER | c.632+2487C>A | FMR1NB | ENSG00000176988.9 | transcript | ENST00000370467.8 | protein_coding | 4/5 | chrX | 148011198 | |||||||
chrX:148011284 | CA | C | 36 | a0001c0001t0001g0034 a0001c0001t0001g0075 a0001c0001t0001g0109 others(33): Show |
39 | HG01168.hp1 HG01891.hp2 HG02257.hp1 others(36): Show |
intron_variant | MODIFIER | c.632+2583delA | FMR1NB | ENSG00000176988.9 | transcript | ENST00000370467.8 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chrX | 148011284 | ||||||
chrX:148011290 | A | C | 1 | a0001c0001t0001g0187 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.632+2579A>C | FMR1NB | ENSG00000176988.9 | transcript | ENST00000370467.8 | protein_coding | 4/5 | chrX | 148011290 | |||||||
chrX:148011455 | A | G | 24 | a0001c0001t0001g0004 a0001c0001t0001g0034 a0001c0001t0001g0047 others(21): Show |
28 | HG00639.hp1 HG01168.hp1 HG01891.hp1 others(25): Show |
intron_variant | MODIFIER | c.632+2744A>G | FMR1NB | ENSG00000176988.9 | transcript | ENST00000370467.8 | protein_coding | 4/5 | chrX | 148011455 | |||||||
chrX:148011473 | T | C | 51 | a0001c0001t0001g0025 a0001c0001t0001g0026 a0001c0001t0001g0034 others(48): Show |
56 | HG01123.hp2 HG01168.hp1 HG01243.hp1 others(53): Show |
intron_variant | MODIFIER | c.632+2762T>C | FMR1NB | ENSG00000176988.9 | transcript | ENST00000370467.8 | protein_coding | 4/5 | chrX | 148011473 | |||||||
chrX:148011515 | A | G | 3 | a0001c0001t0001g0012 a0001c0001t0001g0108 a0001c0001t0002g0193 |
5 | HG02559.hp2 HG02970.hp2 HG03130.hp1 others(2): Show |
intron_variant | MODIFIER | c.632+2804A>G | FMR1NB | ENSG00000176988.9 | transcript | ENST00000370467.8 | protein_coding | 4/5 | chrX | 148011515 | |||||||
chrX:148011674 | G | A | 1 | a0001c0001t0001g0088 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.632+2963G>A | FMR1NB | ENSG00000176988.9 | transcript | ENST00000370467.8 | protein_coding | 4/5 | chrX | 148011674 | |||||||
chrX:148011685 | G | A | 1 | a0002c0002t0001g0048 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.632+2974G>A | FMR1NB | ENSG00000176988.9 | transcript | ENST00000370467.8 | protein_coding | 4/5 | chrX | 148011685 | |||||||
chrX:148011751 | T | G | 8 | a0001c0001t0001g0075 a0001c0001t0001g0115 a0001c0001t0001g0195 others(5): Show |
8 | HG01934.hp1 HG02109.hp1 HG02451.hp1 others(5): Show |
intron_variant | MODIFIER | c.632+3040T>G | FMR1NB | ENSG00000176988.9 | transcript | ENST00000370467.8 | protein_coding | 4/5 | chrX | 148011751 | |||||||
chrX:148011819 | A | G | 1 | a0001c0001t0001g0071 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.632+3108A>G | FMR1NB | ENSG00000176988.9 | transcript | ENST00000370467.8 | protein_coding | 4/5 | chrX | 148011819 | |||||||
chrX:148011825 | A | C | 1 | a0001c0001t0001g0070 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.632+3114A>C | FMR1NB | ENSG00000176988.9 | transcript | ENST00000370467.8 | protein_coding | 4/5 | chrX | 148011825 | |||||||
chrX:148012196 | G | T | 1 | a0001c0001t0001g0075 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.632+3485G>T | FMR1NB | ENSG00000176988.9 | transcript | ENST00000370467.8 | protein_coding | 4/5 | chrX | 148012196 | |||||||
chrX:148012476 | T | A | 1 | a0002c0002t0001g0039 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.632+3765T>A | FMR1NB | ENSG00000176988.9 | transcript | ENST00000370467.8 | protein_coding | 4/5 | chrX | 148012476 | |||||||
chrX:148012481 | T | A | 1 | a0002c0002t0001g0039 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.632+3770T>A | FMR1NB | ENSG00000176988.9 | transcript | ENST00000370467.8 | protein_coding | 4/5 | chrX | 148012481 | |||||||
chrX:148012544 | A | G | 1 | a0002c0002t0001g0175 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.632+3833A>G | FMR1NB | ENSG00000176988.9 | transcript | ENST00000370467.8 | protein_coding | 4/5 | chrX | 148012544 | |||||||
chrX:148012574 | A | G | 1 | a0002c0002t0001g0149 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.632+3863A>G | FMR1NB | ENSG00000176988.9 | transcript | ENST00000370467.8 | protein_coding | 4/5 | chrX | 148012574 | |||||||
chrX:148012775 | T | C | 33 | a0001c0001t0001g0004 a0001c0001t0001g0012 a0001c0001t0001g0026 others(30): Show |
41 | HG00639.hp1 HG01123.hp2 HG01168.hp1 others(38): Show |
intron_variant | MODIFIER | c.632+4064T>C | FMR1NB | ENSG00000176988.9 | transcript | ENST00000370467.8 | protein_coding | 4/5 | chrX | 148012775 | |||||||
chrX:148013015 | G | C | 12 | a0001c0001t0001g0075 a0001c0001t0001g0109 a0001c0001t0001g0110 others(9): Show |
12 | HG01934.hp1 HG02109.hp1 HG02818.hp2 others(9): Show |
intron_variant | MODIFIER | c.632+4304G>C | FMR1NB | ENSG00000176988.9 | transcript | ENST00000370467.8 | protein_coding | 4/5 | chrX | 148013015 | |||||||
chrX:148013156 | T | A | 1 | a0001c0001t0001g0077 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.632+4445T>A | FMR1NB | ENSG00000176988.9 | transcript | ENST00000370467.8 | protein_coding | 4/5 | chrX | 148013156 | |||||||
chrX:148013308 | T | A | 33 | a0001c0001t0001g0004 a0001c0001t0001g0012 a0001c0001t0001g0026 others(30): Show |
41 | HG00639.hp1 HG01123.hp2 HG01168.hp1 others(38): Show |
intron_variant | MODIFIER | c.632+4597T>A | FMR1NB | ENSG00000176988.9 | transcript | ENST00000370467.8 | protein_coding | 4/5 | chrX | 148013308 | |||||||
chrX:148013323 | C | T | 4 | a0002c0002t0001g0116 a0002c0002t0001g0150 a0002c0002t0001g0151 others(1): Show |
4 | HG01081.hp1 HG01106.hp1 HG01346.hp2 others(1): Show |
intron_variant | MODIFIER | c.632+4612C>T | FMR1NB | ENSG00000176988.9 | transcript | ENST00000370467.8 | protein_coding | 4/5 | chrX | 148013323 | |||||||
chrX:148013682 | T | A | 1 | a0002c0002t0001g0039 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.632+4971T>A | FMR1NB | ENSG00000176988.9 | transcript | ENST00000370467.8 | protein_coding | 4/5 | chrX | 148013682 | |||||||
chrX:148013778 | A | C | 1 | a0002c0002t0001g0093 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.632+5067A>C | FMR1NB | ENSG00000176988.9 | transcript | ENST00000370467.8 | protein_coding | 4/5 | chrX | 148013778 | |||||||
chrX:148013812 | C | T | 1 | a0001c0001t0001g0046 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.632+5101C>T | FMR1NB | ENSG00000176988.9 | transcript | ENST00000370467.8 | protein_coding | 4/5 | chrX | 148013812 | |||||||
chrX:148013837 | C | T | 21 | a0001c0001t0001g0004 a0001c0001t0001g0012 a0001c0001t0001g0026 others(18): Show |
29 | HG00639.hp1 HG01123.hp2 HG01168.hp1 others(26): Show |
intron_variant | MODIFIER | c.632+5126C>T | FMR1NB | ENSG00000176988.9 | transcript | ENST00000370467.8 | protein_coding | 4/5 | chrX | 148013837 | |||||||
chrX:148014150 | A | G | 3 | a0001c0001t0001g0110 a0001c0001t0001g0191 a0002c0002t0001g0181 |
3 | HG03486.hp1 HG06807.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.632+5439A>G | FMR1NB | ENSG00000176988.9 | transcript | ENST00000370467.8 | protein_coding | 4/5 | chrX | 148014150 | |||||||
chrX:148014167 | C | T | 1 | a0002c0002t0001g0039 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.632+5456C>T | FMR1NB | ENSG00000176988.9 | transcript | ENST00000370467.8 | protein_coding | 4/5 | chrX | 148014167 | |||||||
chrX:148014173 | G | A | 34 | a0001c0001t0001g0004 a0001c0001t0001g0012 a0001c0001t0001g0026 others(31): Show |
45 | HG00639.hp1 HG01109.hp1 HG01123.hp2 others(42): Show |
intron_variant | MODIFIER | c.632+5462G>A | FMR1NB | ENSG00000176988.9 | transcript | ENST00000370467.8 | protein_coding | 4/5 | chrX | 148014173 | |||||||
chrX:148014198 | C | T | 1 | a0002c0002t0001g0113 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.632+5487C>T | FMR1NB | ENSG00000176988.9 | transcript | ENST00000370467.8 | protein_coding | 4/5 | chrX | 148014198 | |||||||
chrX:148014237 | A | G | 1 | a0002c0002t0001g0114 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.632+5526A>G | FMR1NB | ENSG00000176988.9 | transcript | ENST00000370467.8 | protein_coding | 4/5 | chrX | 148014237 | |||||||
chrX:148014270 | T | G | 6 | a0001c0001t0001g0061 a0001c0001t0001g0062 a0001c0001t0001g0077 others(3): Show |
6 | HG04184.hp2 NA18955.hp1 NA19007.hp1 others(3): Show |
intron_variant | MODIFIER | c.632+5559T>G | FMR1NB | ENSG00000176988.9 | transcript | ENST00000370467.8 | protein_coding | 4/5 | chrX | 148014270 | |||||||
chrX:148014315 | C | A | 1 | a0002c0002t0001g0039 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.632+5604C>A | FMR1NB | ENSG00000176988.9 | transcript | ENST00000370467.8 | protein_coding | 4/5 | chrX | 148014315 | |||||||
chrX:148014378 | C | A | 1 | a0002c0002t0001g0159 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.632+5667C>A | FMR1NB | ENSG00000176988.9 | transcript | ENST00000370467.8 | protein_coding | 4/5 | chrX | 148014378 | |||||||
chrX:148014624 | A | G | 12 | a0001c0001t0001g0110 a0001c0001t0001g0191 a0002c0002t0001g0008 others(9): Show |
15 | HG02451.hp2 HG02615.hp1 HG02723.hp2 others(12): Show |
intron_variant | MODIFIER | c.632+5913A>G | FMR1NB | ENSG00000176988.9 | transcript | ENST00000370467.8 | protein_coding | 4/5 | chrX | 148014624 | |||||||
chrX:148014651 | AT | A | 8 | a0001c0001t0001g0010 a0001c0001t0001g0043 a0001c0001t0001g0068 others(5): Show |
10 | HG03453.hp2 NA18943.hp1 NA18970.hp1 others(7): Show |
intron_variant | MODIFIER | c.632+5951delT | FMR1NB | ENSG00000176988.9 | transcript | ENST00000370467.8 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chrX | 148014651 | ||||||
chrX:148014677 | C | T | 24 | a0001c0001t0001g0004 a0001c0001t0001g0012 a0001c0001t0001g0026 others(21): Show |
32 | HG00639.hp1 HG01109.hp1 HG01123.hp2 others(29): Show |
intron_variant | MODIFIER | c.632+5966C>T | FMR1NB | ENSG00000176988.9 | transcript | ENST00000370467.8 | protein_coding | 4/5 | chrX | 148014677 | |||||||
chrX:148014745 | G | A | 1 | a0002c0002t0001g0125 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.632+6034G>A | FMR1NB | ENSG00000176988.9 | transcript | ENST00000370467.8 | protein_coding | 4/5 | chrX | 148014745 | |||||||
chrX:148014751 | C | G | 3 | a0001c0001t0001g0110 a0001c0001t0001g0191 a0002c0002t0001g0181 |
3 | HG03486.hp1 HG06807.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.632+6040C>G | FMR1NB | ENSG00000176988.9 | transcript | ENST00000370467.8 | protein_coding | 4/5 | chrX | 148014751 | |||||||
chrX:148014761 | C | T | 1 | a0001c0001t0001g0028 | 2 | HG01168.hp2 HG01169.hp1 |
intron_variant | MODIFIER | c.632+6050C>T | FMR1NB | ENSG00000176988.9 | transcript | ENST00000370467.8 | protein_coding | 4/5 | chrX | 148014761 | |||||||
chrX:148015050 | A | T | 44 | a0001c0001t0001g0004 a0001c0001t0001g0012 a0001c0001t0001g0026 others(41): Show |
55 | HG00639.hp1 HG01109.hp1 HG01123.hp2 others(52): Show |
intron_variant | MODIFIER | c.632+6339A>T | FMR1NB | ENSG00000176988.9 | transcript | ENST00000370467.8 | protein_coding | 4/5 | chrX | 148015050 | |||||||
chrX:148015135 | T | C | 1 | a0002c0002t0001g0093 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.632+6424T>C | FMR1NB | ENSG00000176988.9 | transcript | ENST00000370467.8 | protein_coding | 4/5 | chrX | 148015135 | |||||||
chrX:148015316 | A | G | 2 | a0001c0001t0001g0034 a0002c0002t0001g0040 |
2 | HG02486.hp1 HG02818.hp1 |
intron_variant | MODIFIER | c.632+6605A>G | FMR1NB | ENSG00000176988.9 | transcript | ENST00000370467.8 | protein_coding | 4/5 | chrX | 148015316 | |||||||
chrX:148015586 | C | A | 1 | a0002c0002t0001g0101 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.632+6875C>A | FMR1NB | ENSG00000176988.9 | transcript | ENST00000370467.8 | protein_coding | 4/5 | chrX | 148015586 | |||||||
chrX:148015644 | T | C | 1 | a0002c0002t0001g0039 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.632+6933T>C | FMR1NB | ENSG00000176988.9 | transcript | ENST00000370467.8 | protein_coding | 4/5 | chrX | 148015644 | |||||||
chrX:148015795 | G | A | 3 | a0002c0002t0001g0129 a0002c0002t0001g0159 a0002c0002t0001g0160 |
3 | HG00642.hp1 HG01175.hp1 HG01496.hp1 |
intron_variant | MODIFIER | c.632+7084G>A | FMR1NB | ENSG00000176988.9 | transcript | ENST00000370467.8 | protein_coding | 4/5 | chrX | 148015795 | |||||||
chrX:148015825 | G | C | 2 | a0002c0002t0001g0138 a0002c0002t0001g0149 |
2 | NA19065.hp2 NA19068.hp1 |
intron_variant | MODIFIER | c.632+7114G>C | FMR1NB | ENSG00000176988.9 | transcript | ENST00000370467.8 | protein_coding | 4/5 | chrX | 148015825 | |||||||
chrX:148015930 | A | T | 44 | a0001c0001t0001g0004 a0001c0001t0001g0012 a0001c0001t0001g0026 others(41): Show |
55 | HG00639.hp1 HG01109.hp1 HG01123.hp2 others(52): Show |
intron_variant | MODIFIER | c.632+7219A>T | FMR1NB | ENSG00000176988.9 | transcript | ENST00000370467.8 | protein_coding | 4/5 | chrX | 148015930 | |||||||
chrX:148015982 | T | A | 18 | a0001c0001t0001g0065 a0001c0001t0001g0083 a0001c0001t0001g0120 others(15): Show |
19 | HG00140.hp1 HG00408.hp2 HG00597.hp1 others(16): Show |
intron_variant | MODIFIER | c.632+7271T>A | FMR1NB | ENSG00000176988.9 | transcript | ENST00000370467.8 | protein_coding | 4/5 | chrX | 148015982 | |||||||
chrX:148016035 | T | C | 1 | a0001c0001t0001g0201 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.632+7324T>C | FMR1NB | ENSG00000176988.9 | transcript | ENST00000370467.8 | protein_coding | 4/5 | chrX | 148016035 | |||||||
chrX:148016096 | G | T | 1 | a0002c0002t0001g0169 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.632+7385G>T | FMR1NB | ENSG00000176988.9 | transcript | ENST00000370467.8 | protein_coding | 4/5 | chrX | 148016096 | |||||||
chrX:148016096 | GATTTTTT others(138): Show |
G | 2 | a0001c0001t0001g0137 a0002c0002t0001g0031 |
2 | HG02273.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.632+7417_632+7561d others(2): Show |
FMR1NB | ENSG00000176988.9 | transcript | ENST00000370467.8 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chrX | 148016096 | ||||||
chrX:148016160 | C | CT | 209 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(206): Show |
271 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(268): Show |
intron_variant | MODIFIER | c.632+7455dupT | FMR1NB | ENSG00000176988.9 | transcript | ENST00000370467.8 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chrX | 148016160 | ||||||
chrX:148016176 | A | G | 1 | a0001c0001t0001g0028 | 2 | HG01168.hp2 HG01169.hp1 |
intron_variant | MODIFIER | c.632+7465A>G | FMR1NB | ENSG00000176988.9 | transcript | ENST00000370467.8 | protein_coding | 4/5 | chrX | 148016176 | |||||||
chrX:148016512 | C | T | 1 | a0001c0001t0001g0046 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.632+7801C>T | FMR1NB | ENSG00000176988.9 | transcript | ENST00000370467.8 | protein_coding | 4/5 | chrX | 148016512 | |||||||
chrX:148016541 | C | A | 1 | a0002c0002t0001g0163 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.632+7830C>A | FMR1NB | ENSG00000176988.9 | transcript | ENST00000370467.8 | protein_coding | 4/5 | chrX | 148016541 | |||||||
chrX:148016626 | G | T | 1 | a0002c0002t0001g0165 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.632+7915G>T | FMR1NB | ENSG00000176988.9 | transcript | ENST00000370467.8 | protein_coding | 4/5 | chrX | 148016626 | |||||||
chrX:148016746 | C | T | 1 | a0001c0001t0001g0062 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.632+8035C>T | FMR1NB | ENSG00000176988.9 | transcript | ENST00000370467.8 | protein_coding | 4/5 | chrX | 148016746 | |||||||
chrX:148016801 | A | G | 6 | a0001c0001t0001g0075 a0001c0001t0001g0115 a0001c0001t0001g0195 others(3): Show |
6 | HG01934.hp1 HG02109.hp1 HG02970.hp1 others(3): Show |
intron_variant | MODIFIER | c.633-8064A>G | FMR1NB | ENSG00000176988.9 | transcript | ENST00000370467.8 | protein_coding | 4/5 | chrX | 148016801 | |||||||
chrX:148016857 | C | T | 11 | a0001c0001t0001g0115 a0002c0002t0001g0008 a0002c0002t0001g0017 others(8): Show |
14 | HG01934.hp1 HG02109.hp1 HG02615.hp1 others(11): Show |
intron_variant | MODIFIER | c.633-8008C>T | FMR1NB | ENSG00000176988.9 | transcript | ENST00000370467.8 | protein_coding | 4/5 | chrX | 148016857 | |||||||
chrX:148017096 | C | A | 1 | a0001c0001t0001g0075 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.633-7769C>A | FMR1NB | ENSG00000176988.9 | transcript | ENST00000370467.8 | protein_coding | 4/5 | chrX | 148017096 | |||||||
chrX:148017479 | T | C | 2 | a0002c0002t0001g0135 a0002c0002t0001g0145 |
2 | HG00323.hp2 HG01081.hp2 |
intron_variant | MODIFIER | c.633-7386T>C | FMR1NB | ENSG00000176988.9 | transcript | ENST00000370467.8 | protein_coding | 4/5 | chrX | 148017479 | |||||||
chrX:148017532 | T | C | 1 | a0002c0002t0001g0101 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.633-7333T>C | FMR1NB | ENSG00000176988.9 | transcript | ENST00000370467.8 | protein_coding | 4/5 | chrX | 148017532 | |||||||
chrX:148017546 | T | A | 14 | a0001c0001t0001g0109 a0001c0001t0001g0195 a0002c0002t0001g0008 others(11): Show |
17 | HG02257.hp1 HG02451.hp2 HG02615.hp1 others(14): Show |
intron_variant | MODIFIER | c.633-7319T>A | FMR1NB | ENSG00000176988.9 | transcript | ENST00000370467.8 | protein_coding | 4/5 | chrX | 148017546 | |||||||
chrX:148017645 | G | A | 2 | a0001c0001t0001g0195 a0001c0001t0002g0193 |
2 | HG03041.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.633-7220G>A | FMR1NB | ENSG00000176988.9 | transcript | ENST00000370467.8 | protein_coding | 4/5 | chrX | 148017645 | |||||||
chrX:148017670 | C | G | 1 | a0002c0002t0001g0039 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.633-7195C>G | FMR1NB | ENSG00000176988.9 | transcript | ENST00000370467.8 | protein_coding | 4/5 | chrX | 148017670 | |||||||
chrX:148017691 | C | T | 1 | a0001c0001t0001g0204 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.633-7174C>T | FMR1NB | ENSG00000176988.9 | transcript | ENST00000370467.8 | protein_coding | 4/5 | chrX | 148017691 | |||||||
chrX:148017693 | C | T | 1 | a0001c0001t0001g0204 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.633-7172C>T | FMR1NB | ENSG00000176988.9 | transcript | ENST00000370467.8 | protein_coding | 4/5 | chrX | 148017693 | |||||||
chrX:148017874 | AT | A | 8 | a0002c0002t0001g0008 a0002c0002t0001g0017 a0002c0002t0001g0048 others(5): Show |
11 | HG02615.hp1 HG02723.hp2 HG02886.hp1 others(8): Show |
intron_variant | MODIFIER | c.633-6985delT | FMR1NB | ENSG00000176988.9 | transcript | ENST00000370467.8 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chrX | 148017874 | ||||||
chrX:148017988 | C | T | 5 | a0001c0001t0001g0115 a0002c0002t0001g0033 a0002c0002t0001g0039 others(2): Show |
5 | HG01934.hp1 HG02109.hp1 HG02257.hp1 others(2): Show |
intron_variant | MODIFIER | c.633-6877C>T | FMR1NB | ENSG00000176988.9 | transcript | ENST00000370467.8 | protein_coding | 4/5 | chrX | 148017988 | |||||||
chrX:148018002 | G | A | 1 | a0001c0001t0001g0006 | 4 | NA18941.hp1 NA18947.hp2 NA18988.hp1 others(1): Show |
intron_variant | MODIFIER | c.633-6863G>A | FMR1NB | ENSG00000176988.9 | transcript | ENST00000370467.8 | protein_coding | 4/5 | chrX | 148018002 | |||||||
chrX:148018163 | G | A | 44 | a0001c0001t0001g0004 a0001c0001t0001g0012 a0001c0001t0001g0026 others(41): Show |
55 | HG00639.hp1 HG01109.hp1 HG01123.hp2 others(52): Show |
intron_variant | MODIFIER | c.633-6702G>A | FMR1NB | ENSG00000176988.9 | transcript | ENST00000370467.8 | protein_coding | 4/5 | chrX | 148018163 | |||||||
chrX:148018175 | A | G | 1 | a0001c0001t0001g0190 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.633-6690A>G | FMR1NB | ENSG00000176988.9 | transcript | ENST00000370467.8 | protein_coding | 4/5 | chrX | 148018175 | |||||||
chrX:148018188 | C | G | 13 | a0001c0001t0001g0004 a0001c0001t0001g0012 a0001c0001t0001g0047 others(10): Show |
20 | HG00639.hp1 HG01884.hp2 HG01891.hp2 others(17): Show |
intron_variant | MODIFIER | c.633-6677C>G | FMR1NB | ENSG00000176988.9 | transcript | ENST00000370467.8 | protein_coding | 4/5 | chrX | 148018188 | |||||||
chrX:148018247 | G | T | 4 | a0001c0001t0001g0010 a0001c0001t0001g0194 a0001c0001t0001g0211 others(1): Show |
6 | HG02622.hp2 NA18943.hp1 NA18970.hp1 others(3): Show |
intron_variant | MODIFIER | c.633-6618G>T | FMR1NB | ENSG00000176988.9 | transcript | ENST00000370467.8 | protein_coding | 4/5 | chrX | 148018247 | |||||||
chrX:148018596 | G | C | 6 | a0001c0001t0001g0075 a0001c0001t0001g0115 a0001c0001t0001g0195 others(3): Show |
6 | HG01934.hp1 HG02109.hp1 HG02970.hp1 others(3): Show |
intron_variant | MODIFIER | c.633-6269G>C | FMR1NB | ENSG00000176988.9 | transcript | ENST00000370467.8 | protein_coding | 4/5 | chrX | 148018596 | |||||||
chrX:148018743 | C | A | 1 | a0001c0001t0002g0193 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.633-6122C>A | FMR1NB | ENSG00000176988.9 | transcript | ENST00000370467.8 | protein_coding | 4/5 | chrX | 148018743 | |||||||
chrX:148019256 | A | G | 22 | a0001c0001t0001g0004 a0001c0001t0001g0012 a0001c0001t0001g0026 others(19): Show |
30 | HG00639.hp1 HG01109.hp1 HG01123.hp2 others(27): Show |
intron_variant | MODIFIER | c.633-5609A>G | FMR1NB | ENSG00000176988.9 | transcript | ENST00000370467.8 | protein_coding | 4/5 | chrX | 148019256 | |||||||
chrX:148019271 | T | G | 1 | a0001c0001t0001g0183 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.633-5594T>G | FMR1NB | ENSG00000176988.9 | transcript | ENST00000370467.8 | protein_coding | 4/5 | chrX | 148019271 | |||||||
chrX:148019340 | A | T | 1 | a0002c0002t0001g0038 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.633-5525A>T | FMR1NB | ENSG00000176988.9 | transcript | ENST00000370467.8 | protein_coding | 4/5 | chrX | 148019340 | |||||||
chrX:148019376 | T | C | 1 | a0001c0001t0001g0081 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.633-5489T>C | FMR1NB | ENSG00000176988.9 | transcript | ENST00000370467.8 | protein_coding | 4/5 | chrX | 148019376 | |||||||
chrX:148019383 | T | C | 36 | a0001c0001t0001g0004 a0001c0001t0001g0012 a0001c0001t0001g0026 others(33): Show |
44 | HG00639.hp1 HG01109.hp1 HG01123.hp2 others(41): Show |
intron_variant | MODIFIER | c.633-5482T>C | FMR1NB | ENSG00000176988.9 | transcript | ENST00000370467.8 | protein_coding | 4/5 | chrX | 148019383 | |||||||
chrX:148019466 | A | G | 1 | a0002c0002t0001g0039 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.633-5399A>G | FMR1NB | ENSG00000176988.9 | transcript | ENST00000370467.8 | protein_coding | 4/5 | chrX | 148019466 | |||||||
chrX:148019510 | T | C | 1 | a0002c0002t0001g0038 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.633-5355T>C | FMR1NB | ENSG00000176988.9 | transcript | ENST00000370467.8 | protein_coding | 4/5 | chrX | 148019510 | |||||||
chrX:148019545 | T | C | 9 | a0002c0002t0001g0008 a0002c0002t0001g0017 a0002c0002t0001g0038 others(6): Show |
12 | HG02451.hp2 HG02615.hp1 HG02723.hp2 others(9): Show |
intron_variant | MODIFIER | c.633-5320T>C | FMR1NB | ENSG00000176988.9 | transcript | ENST00000370467.8 | protein_coding | 4/5 | chrX | 148019545 | |||||||
chrX:148019807 | C | A | 8 | a0002c0002t0001g0008 a0002c0002t0001g0017 a0002c0002t0001g0048 others(5): Show |
11 | HG02615.hp1 HG02723.hp2 HG02886.hp1 others(8): Show |
intron_variant | MODIFIER | c.633-5058C>A | FMR1NB | ENSG00000176988.9 | transcript | ENST00000370467.8 | protein_coding | 4/5 | chrX | 148019807 | |||||||
chrX:148019878 | T | A | 1 | a0002c0002t0001g0146 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.633-4987T>A | FMR1NB | ENSG00000176988.9 | transcript | ENST00000370467.8 | protein_coding | 4/5 | chrX | 148019878 | |||||||
chrX:148019955 | G | A | 3 | a0001c0001t0001g0110 a0001c0001t0001g0191 a0002c0002t0001g0181 |
3 | HG03486.hp1 HG06807.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.633-4910G>A | FMR1NB | ENSG00000176988.9 | transcript | ENST00000370467.8 | protein_coding | 4/5 | chrX | 148019955 | |||||||
chrX:148020086 | G | A | 1 | a0001c0001t0001g0088 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.633-4779G>A | FMR1NB | ENSG00000176988.9 | transcript | ENST00000370467.8 | protein_coding | 4/5 | chrX | 148020086 | |||||||
chrX:148020148 | TTTCTACA others(20): Show |
T | 3 | a0001c0001t0001g0115 a0002c0002t0001g0033 a0002c0002t0001g0171 |
3 | HG01934.hp1 HG02109.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.633-4715_633-4689d others(29): Show |
FMR1NB | ENSG00000176988.9 | transcript | ENST00000370467.8 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chrX | 148020148 | ||||||
chrX:148020302 | C | T | 3 | a0001c0001t0001g0059 a0001c0001t0001g0204 a0001c0001t0001g0209 |
3 | HG02056.hp1 HG02080.hp1 NA18992.hp1 |
intron_variant | MODIFIER | c.633-4563C>T | FMR1NB | ENSG00000176988.9 | transcript | ENST00000370467.8 | protein_coding | 4/5 | chrX | 148020302 | |||||||
chrX:148020588 | A | C | 1 | a0001c0001t0002g0193 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.633-4277A>C | FMR1NB | ENSG00000176988.9 | transcript | ENST00000370467.8 | protein_coding | 4/5 | chrX | 148020588 | |||||||
chrX:148020728 | G | A | 24 | a0001c0001t0001g0004 a0001c0001t0001g0012 a0001c0001t0001g0026 others(21): Show |
32 | HG00639.hp1 HG01109.hp1 HG01123.hp2 others(29): Show |
intron_variant | MODIFIER | c.633-4137G>A | FMR1NB | ENSG00000176988.9 | transcript | ENST00000370467.8 | protein_coding | 4/5 | chrX | 148020728 | |||||||
chrX:148020878 | T | C | 1 | a0002c0002t0001g0039 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.633-3987T>C | FMR1NB | ENSG00000176988.9 | transcript | ENST00000370467.8 | protein_coding | 4/5 | chrX | 148020878 | |||||||
chrX:148021117 | C | G | 4 | a0002c0002t0001g0119 a0002c0002t0001g0142 a0002c0002t0001g0144 others(1): Show |
4 | HG02145.hp1 HG02717.hp1 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.633-3748C>G | FMR1NB | ENSG00000176988.9 | transcript | ENST00000370467.8 | protein_coding | 4/5 | chrX | 148021117 | |||||||
chrX:148021293 | A | G | 1 | a0002c0002t0001g0148 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.633-3572A>G | FMR1NB | ENSG00000176988.9 | transcript | ENST00000370467.8 | protein_coding | 4/5 | chrX | 148021293 | |||||||
chrX:148021324 | A | T | 2 | a0001c0001t0001g0034 a0002c0002t0001g0040 |
2 | HG02486.hp1 HG02818.hp1 |
intron_variant | MODIFIER | c.633-3541A>T | FMR1NB | ENSG00000176988.9 | transcript | ENST00000370467.8 | protein_coding | 4/5 | chrX | 148021324 | |||||||
chrX:148021383 | T | C | 1 | a0001c0001t0001g0183 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.633-3482T>C | FMR1NB | ENSG00000176988.9 | transcript | ENST00000370467.8 | protein_coding | 4/5 | chrX | 148021383 | |||||||
chrX:148021397 | C | CT | 6 | a0001c0001t0001g0186 a0001c0001t0001g0199 a0002c0002t0001g0008 others(3): Show |
8 | HG01069.hp1 HG02615.hp1 HG02723.hp2 others(5): Show |
intron_variant | MODIFIER | c.633-3453dupT | FMR1NB | ENSG00000176988.9 | transcript | ENST00000370467.8 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chrX | 148021397 | ||||||
chrX:148021397 | CT | C | 9 | a0001c0001t0001g0075 a0001c0001t0001g0110 a0001c0001t0001g0115 others(6): Show |
9 | HG02258.hp1 HG02451.hp2 HG02970.hp1 others(6): Show |
intron_variant | MODIFIER | c.633-3453delT | FMR1NB | ENSG00000176988.9 | transcript | ENST00000370467.8 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chrX | 148021397 | ||||||
chrX:148021397 | CTT | C | 24 | a0001c0001t0001g0004 a0001c0001t0001g0012 a0001c0001t0001g0026 others(21): Show |
32 | HG00639.hp1 HG01109.hp1 HG01123.hp2 others(29): Show |
intron_variant | MODIFIER | c.633-3454_633-3453d others(4): Show |
FMR1NB | ENSG00000176988.9 | transcript | ENST00000370467.8 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chrX | 148021397 | ||||||
chrX:148021781 | CCTCCAGC others(10): Show |
C | 30 | a0001c0001t0001g0004 a0001c0001t0001g0012 a0001c0001t0001g0026 others(27): Show |
38 | HG00639.hp1 HG01109.hp1 HG01123.hp2 others(35): Show |
intron_variant | MODIFIER | c.633-3081_633-3065d others(19): Show |
FMR1NB | ENSG00000176988.9 | transcript | ENST00000370467.8 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chrX | 148021781 | ||||||
chrX:148021896 | CT | C | 5 | a0001c0001t0001g0061 a0001c0001t0001g0062 a0001c0001t0001g0079 others(2): Show |
5 | HG03453.hp1 HG04184.hp2 NA19007.hp1 others(2): Show |
intron_variant | MODIFIER | c.633-2954delT | FMR1NB | ENSG00000176988.9 | transcript | ENST00000370467.8 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chrX | 148021896 | ||||||
chrX:148022102 | T | C | 1 | a0001c0001t0001g0018 | 2 | NA18977.hp1 NA18998.hp2 |
intron_variant | MODIFIER | c.633-2763T>C | FMR1NB | ENSG00000176988.9 | transcript | ENST00000370467.8 | protein_coding | 4/5 | chrX | 148022102 | |||||||
chrX:148022137 | C | G | 1 | a0002c0002t0001g0180 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.633-2728C>G | FMR1NB | ENSG00000176988.9 | transcript | ENST00000370467.8 | protein_coding | 4/5 | chrX | 148022137 | |||||||
chrX:148022192 | C | A | 2 | a0001c0001t0001g0012 a0001c0001t0001g0108 |
4 | HG02559.hp2 HG02970.hp2 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.633-2673C>A | FMR1NB | ENSG00000176988.9 | transcript | ENST00000370467.8 | protein_coding | 4/5 | chrX | 148022192 | |||||||
chrX:148022249 | CA | C | 30 | a0001c0001t0001g0004 a0001c0001t0001g0012 a0001c0001t0001g0026 others(27): Show |
38 | HG00639.hp1 HG01109.hp1 HG01123.hp2 others(35): Show |
intron_variant | MODIFIER | c.633-2615delA | FMR1NB | ENSG00000176988.9 | transcript | ENST00000370467.8 | protein_coding | 4/5 | chrX | 148022249 | |||||||
chrX:148022545 | C | T | 1 | a0002c0002t0001g0146 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.633-2320C>T | FMR1NB | ENSG00000176988.9 | transcript | ENST00000370467.8 | protein_coding | 4/5 | chrX | 148022545 | |||||||
chrX:148022627 | C | T | 30 | a0001c0001t0001g0004 a0001c0001t0001g0012 a0001c0001t0001g0026 others(27): Show |
38 | HG00639.hp1 HG01109.hp1 HG01123.hp2 others(35): Show |
intron_variant | MODIFIER | c.633-2238C>T | FMR1NB | ENSG00000176988.9 | transcript | ENST00000370467.8 | protein_coding | 4/5 | chrX | 148022627 | |||||||
chrX:148022679 | C | T | 6 | a0001c0001t0001g0075 a0001c0001t0001g0110 a0001c0001t0001g0191 others(3): Show |
6 | HG03041.hp2 HG03486.hp1 HG03540.hp1 others(3): Show |
intron_variant | MODIFIER | c.633-2186C>T | FMR1NB | ENSG00000176988.9 | transcript | ENST00000370467.8 | protein_coding | 4/5 | chrX | 148022679 | |||||||
chrX:148022727 | G | C | 30 | a0001c0001t0001g0004 a0001c0001t0001g0012 a0001c0001t0001g0026 others(27): Show |
38 | HG00639.hp1 HG01109.hp1 HG01123.hp2 others(35): Show |
intron_variant | MODIFIER | c.633-2138G>C | FMR1NB | ENSG00000176988.9 | transcript | ENST00000370467.8 | protein_coding | 4/5 | chrX | 148022727 | |||||||
chrX:148022849 | TAAAG | T | 6 | a0001c0001t0001g0115 a0002c0002t0001g0033 a0002c0002t0001g0038 others(3): Show |
6 | HG01934.hp1 HG02109.hp1 HG02257.hp1 others(3): Show |
intron_variant | MODIFIER | c.633-2012_633-2009d others(6): Show |
FMR1NB | ENSG00000176988.9 | transcript | ENST00000370467.8 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chrX | 148022849 | ||||||
chrX:148023296 | A | C | 8 | a0002c0002t0001g0008 a0002c0002t0001g0017 a0002c0002t0001g0048 others(5): Show |
11 | HG02615.hp1 HG02723.hp2 HG02886.hp1 others(8): Show |
intron_variant | MODIFIER | c.633-1569A>C | FMR1NB | ENSG00000176988.9 | transcript | ENST00000370467.8 | protein_coding | 4/5 | chrX | 148023296 | |||||||
chrX:148023363 | G | T | 1 | a0001c0001t0001g0115 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.633-1502G>T | FMR1NB | ENSG00000176988.9 | transcript | ENST00000370467.8 | protein_coding | 4/5 | chrX | 148023363 | |||||||
chrX:148023457 | T | C | 2 | a0001c0001t0001g0109 a0002c0002t0001g0208 |
2 | HG02818.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.633-1408T>C | FMR1NB | ENSG00000176988.9 | transcript | ENST00000370467.8 | protein_coding | 4/5 | chrX | 148023457 | |||||||
chrX:148023484 | A | G | 1 | a0002c0002t0001g0038 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.633-1381A>G | FMR1NB | ENSG00000176988.9 | transcript | ENST00000370467.8 | protein_coding | 4/5 | chrX | 148023484 | |||||||
chrX:148023497 | T | TGGGACCC others(3): Show |
1 | a0001c0001t0001g0186 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.633-1367_633-1358d others(12): Show |
FMR1NB | ENSG00000176988.9 | transcript | ENST00000370467.8 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chrX | 148023497 | ||||||
chrX:148023537 | A | AACT | 14 | a0001c0001t0001g0075 a0001c0001t0001g0110 a0001c0001t0001g0191 others(11): Show |
17 | HG02615.hp1 HG02723.hp2 HG02886.hp1 others(14): Show |
intron_variant | MODIFIER | c.633-1327_633-1326i others(5): Show |
FMR1NB | ENSG00000176988.9 | transcript | ENST00000370467.8 | protein_coding | 4/5 | INFO_REALIGN_3_PRIME | chrX | 148023537 | ||||||
chrX:148023655 | T | C | 21 | a0001c0001t0001g0004 a0001c0001t0001g0012 a0001c0001t0001g0026 others(18): Show |
29 | HG00639.hp1 HG01123.hp2 HG01168.hp1 others(26): Show |
intron_variant | MODIFIER | c.633-1210T>C | FMR1NB | ENSG00000176988.9 | transcript | ENST00000370467.8 | protein_coding | 4/5 | chrX | 148023655 | |||||||
chrX:148024070 | T | C | 5 | a0002c0002t0001g0097 a0002c0002t0001g0100 a0002c0002t0001g0102 others(2): Show |
5 | HG03017.hp1 HG03491.hp1 HG03669.hp2 others(2): Show |
intron_variant | MODIFIER | c.633-795T>C | FMR1NB | ENSG00000176988.9 | transcript | ENST00000370467.8 | protein_coding | 4/5 | chrX | 148024070 | |||||||
chrX:148024092 | C | A | 2 | a0001c0001t0001g0109 a0002c0002t0001g0208 |
2 | HG02818.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.633-773C>A | FMR1NB | ENSG00000176988.9 | transcript | ENST00000370467.8 | protein_coding | 4/5 | chrX | 148024092 | |||||||
chrX:148024099 | C | T | 1 | a0001c0001t0001g0062 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.633-766C>T | FMR1NB | ENSG00000176988.9 | transcript | ENST00000370467.8 | protein_coding | 4/5 | chrX | 148024099 | |||||||
chrX:148024132 | T | G | 6 | a0001c0001t0001g0075 a0001c0001t0001g0110 a0001c0001t0001g0191 others(3): Show |
6 | HG03041.hp2 HG03486.hp1 HG03540.hp1 others(3): Show |
intron_variant | MODIFIER | c.633-733T>G | FMR1NB | ENSG00000176988.9 | transcript | ENST00000370467.8 | protein_coding | 4/5 | chrX | 148024132 | |||||||
chrX:148024142 | A | G | 1 | a0002c0002t0001g0145 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.633-723A>G | FMR1NB | ENSG00000176988.9 | transcript | ENST00000370467.8 | protein_coding | 4/5 | chrX | 148024142 | |||||||
chrX:148024400 | A | G | 6 | a0001c0001t0001g0075 a0001c0001t0001g0110 a0001c0001t0001g0191 others(3): Show |
6 | HG03041.hp2 HG03486.hp1 HG03540.hp1 others(3): Show |
intron_variant | MODIFIER | c.633-465A>G | FMR1NB | ENSG00000176988.9 | transcript | ENST00000370467.8 | protein_coding | 4/5 | chrX | 148024400 | |||||||
chrX:148024426 | G | A | 8 | a0002c0002t0001g0008 a0002c0002t0001g0017 a0002c0002t0001g0048 others(5): Show |
11 | HG02615.hp1 HG02723.hp2 HG02886.hp1 others(8): Show |
intron_variant | MODIFIER | c.633-439G>A | FMR1NB | ENSG00000176988.9 | transcript | ENST00000370467.8 | protein_coding | 4/5 | chrX | 148024426 | |||||||
chrX:148024635 | T | A | 45 | a0001c0001t0001g0004 a0001c0001t0001g0012 a0001c0001t0001g0026 others(42): Show |
56 | HG00639.hp1 HG01109.hp1 HG01123.hp2 others(53): Show |
intron_variant | MODIFIER | c.633-230T>A | FMR1NB | ENSG00000176988.9 | transcript | ENST00000370467.8 | protein_coding | 4/5 | chrX | 148024635 | |||||||
chrX:148025036 | G | T | 1 | a0001c0001t0001g0089 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.*13+23G>T | FMR1NB | ENSG00000176988.9 | transcript | ENST00000370467.8 | protein_coding | 5/5 | chrX | 148025036 | |||||||
chrX:148025405 | A | C | 30 | a0001c0001t0001g0004 a0001c0001t0001g0012 a0001c0001t0001g0026 others(27): Show |
38 | HG00639.hp1 HG01109.hp1 HG01123.hp2 others(35): Show |
intron_variant | MODIFIER | c.*13+392A>C | FMR1NB | ENSG00000176988.9 | transcript | ENST00000370467.8 | protein_coding | 5/5 | chrX | 148025405 | |||||||
chrX:148025509 | C | T | 3 | a0001c0001t0001g0115 a0002c0002t0001g0033 a0002c0002t0001g0171 |
3 | HG01934.hp1 HG02109.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.*13+496C>T | FMR1NB | ENSG00000176988.9 | transcript | ENST00000370467.8 | protein_coding | 5/5 | chrX | 148025509 | |||||||
chrX:148025625 | G | C | 8 | a0002c0002t0001g0008 a0002c0002t0001g0017 a0002c0002t0001g0048 others(5): Show |
11 | HG02615.hp1 HG02723.hp2 HG02886.hp1 others(8): Show |
intron_variant | MODIFIER | c.*13+612G>C | FMR1NB | ENSG00000176988.9 | transcript | ENST00000370467.8 | protein_coding | 5/5 | chrX | 148025625 | |||||||
chrX:148025736 | A | G | 1 | a0002c0002t0001g0142 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.*13+723A>G | FMR1NB | ENSG00000176988.9 | transcript | ENST00000370467.8 | protein_coding | 5/5 | chrX | 148025736 | |||||||
chrX:148025864 | G | A | 30 | a0001c0001t0001g0004 a0001c0001t0001g0012 a0001c0001t0001g0026 others(27): Show |
38 | HG00639.hp1 HG01109.hp1 HG01123.hp2 others(35): Show |
intron_variant | MODIFIER | c.*14-638G>A | FMR1NB | ENSG00000176988.9 | transcript | ENST00000370467.8 | protein_coding | 5/5 | chrX | 148025864 | |||||||
chrX:148025992 | G | A | 1 | a0001c0001t0001g0066 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.*14-510G>A | FMR1NB | ENSG00000176988.9 | transcript | ENST00000370467.8 | protein_coding | 5/5 | chrX | 148025992 | |||||||
chrX:148025994 | A | G | 63 | a0001c0001t0001g0003 a0001c0001t0001g0019 a0001c0001t0001g0044 others(60): Show |
74 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(71): Show |
intron_variant | MODIFIER | c.*14-508A>G | FMR1NB | ENSG00000176988.9 | transcript | ENST00000370467.8 | protein_coding | 5/5 | chrX | 148025994 | |||||||
chrX:148026064 | T | C | 1 | a0001c0001t0001g0183 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.*14-438T>C | FMR1NB | ENSG00000176988.9 | transcript | ENST00000370467.8 | protein_coding | 5/5 | chrX | 148026064 | |||||||
chrX:148026091 | G | T | 1 | a0002c0002t0001g0160 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.*14-411G>T | FMR1NB | ENSG00000176988.9 | transcript | ENST00000370467.8 | protein_coding | 5/5 | chrX | 148026091 | |||||||
chrX:148026125 | T | C | 24 | a0001c0001t0001g0004 a0001c0001t0001g0012 a0001c0001t0001g0026 others(21): Show |
32 | HG00639.hp1 HG01109.hp1 HG01123.hp2 others(29): Show |
intron_variant | MODIFIER | c.*14-377T>C | FMR1NB | ENSG00000176988.9 | transcript | ENST00000370467.8 | protein_coding | 5/5 | chrX | 148026125 | |||||||
chrX:148026289 | T | A | 6 | a0001c0001t0001g0075 a0001c0001t0001g0110 a0001c0001t0001g0191 others(3): Show |
6 | HG03041.hp2 HG03486.hp1 HG03540.hp1 others(3): Show |
intron_variant | MODIFIER | c.*14-213T>A | FMR1NB | ENSG00000176988.9 | transcript | ENST00000370467.8 | protein_coding | 5/5 | chrX | 148026289 | |||||||
chrX:148026308 | T | G | 1 | a0001c0001t0001g0068 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.*14-194T>G | FMR1NB | ENSG00000176988.9 | transcript | ENST00000370467.8 | protein_coding | 5/5 | chrX | 148026308 | |||||||
chrX:148026421 | G | T | 2 | a0001c0001t0001g0109 a0002c0002t0001g0208 |
2 | HG02818.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.*14-81G>T | FMR1NB | ENSG00000176988.9 | transcript | ENST00000370467.8 | protein_coding | 5/5 | chrX | 148026421 | |||||||
chrX:148026496 | C | T | 1 | a0002c0002t0001g0170 | 1 | NA18947.hp1 | splice_region_variant&intron_variant | LOW | c.*14-6C>T | FMR1NB | ENSG00000176988.9 | transcript | ENST00000370467.8 | protein_coding | 5/5 | chrX | 148026496 |