geneid | 79589 |
---|---|
ensemblid | ENSG00000133135.14 |
hgncid | 21153 |
symbol | RNF128 |
name | ring finger protein 128 |
refseq_nuc | NM_194463.2 |
refseq_prot | NP_919445.1 |
ensembl_nuc | ENST00000255499.3 |
ensembl_prot | ENSP00000255499.2 |
mane_status | MANE Select |
chr | chrX |
start | 106726701 |
end | 106797016 |
strand | + |
ver | v1.2 |
region | chrX:106726701-106797016 |
region5000 | chrX:106721701-106802016 |
regionname0 | RNF128_chrX_106726701_106797016 |
regionname5000 | RNF128_chrX_106721701_106802016 |
ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 1/1 | 428 | 207 | 64 | 41 | 73 | 7 | 20 | 52 | RNF128_chrX_106721701_106802016 | RNF128 | copy fasta | chrX | 106721701 | 106802016 |
a0002 | 0/0 | 428 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | RNF128_chrX_106721701_106802016 | RNF128 | copy fasta | chrX | 106721701 | 106802016 |
a0003 | 0/0 | 428 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | RNF128_chrX_106721701_106802016 | RNF128 | copy fasta | chrX | 106721701 | 106802016 |
chapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
c0001 | 1/1 | 1287 | 207 | 64 | 41 | 73 | 7 | 20 | RNF128_chrX_106721701_106802016 | RNF128 | copy fasta | chrX | 106721701 | 106802016 |
c0002 | 0/0 | 1287 | 1 | 0 | 0 | 1 | 0 | 0 | RNF128_chrX_106721701_106802016 | RNF128 | copy fasta | chrX | 106721701 | 106802016 |
c0003 | 0/0 | 1287 | 1 | 0 | 0 | 1 | 0 | 0 | RNF128_chrX_106721701_106802016 | RNF128 | copy fasta | chrX | 106721701 | 106802016 |
thapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
t0001 | 1/1 | 1517 | 182 | 47 | 40 | 67 | 7 | 19 | RNF128_chrX_106721701_106802016 | RNF128 | copy fasta | chrX | 106721701 | 106802016 |
t0002 | 0/0 | 1517 | 17 | 16 | 1 | 0 | 0 | 0 | RNF128_chrX_106721701_106802016 | RNF128 | copy fasta | chrX | 106721701 | 106802016 |
t0003 | 0/0 | 1517 | 6 | 0 | 0 | 6 | 0 | 0 | RNF128_chrX_106721701_106802016 | RNF128 | copy fasta | chrX | 106721701 | 106802016 |
t0004 | 0/0 | 1516 | 1 | 0 | 0 | 1 | 0 | 0 | RNF128_chrX_106721701_106802016 | RNF128 | copy fasta | chrX | 106721701 | 106802016 |
t0005 | 0/0 | 1517 | 1 | 1 | 0 | 0 | 0 | 0 | RNF128_chrX_106721701_106802016 | RNF128 | copy fasta | chrX | 106721701 | 106802016 |
t0006 | 0/0 | 1517 | 1 | 0 | 0 | 0 | 0 | 1 | RNF128_chrX_106721701_106802016 | RNF128 | copy fasta | chrX | 106721701 | 106802016 |
t0007 | 0/0 | 1516 | 1 | 0 | 0 | 1 | 0 | 0 | RNF128_chrX_106721701_106802016 | RNF128 | copy fasta | chrX | 106721701 | 106802016 |
ghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
g0001 | 0/0 | 7 | 1 | 0 | 5 | 0 | 1 | RNF128_chrX_106721701_106802016 | RNF128 | chrX | 106721701 | 106802016 |
g0002 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | RNF128_chrX_106721701_106802016 | RNF128 | chrX | 106721701 | 106802016 |
g0003 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | RNF128_chrX_106721701_106802016 | RNF128 | chrX | 106721701 | 106802016 |
g0004 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | RNF128_chrX_106721701_106802016 | RNF128 | chrX | 106721701 | 106802016 |
g0005 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | RNF128_chrX_106721701_106802016 | RNF128 | chrX | 106721701 | 106802016 |
g0006 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | RNF128_chrX_106721701_106802016 | RNF128 | chrX | 106721701 | 106802016 |
g0007 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RNF128_chrX_106721701_106802016 | RNF128 | chrX | 106721701 | 106802016 |
g0008 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RNF128_chrX_106721701_106802016 | RNF128 | chrX | 106721701 | 106802016 |
g0009 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | RNF128_chrX_106721701_106802016 | RNF128 | chrX | 106721701 | 106802016 |
g0010 | 0/0 | 2 | 1 | 0 | 0 | 1 | 0 | RNF128_chrX_106721701_106802016 | RNF128 | chrX | 106721701 | 106802016 |
g0011 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | RNF128_chrX_106721701_106802016 | RNF128 | chrX | 106721701 | 106802016 |
g0012 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RNF128_chrX_106721701_106802016 | RNF128 | chrX | 106721701 | 106802016 |
g0013 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RNF128_chrX_106721701_106802016 | RNF128 | chrX | 106721701 | 106802016 |
g0014 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | RNF128_chrX_106721701_106802016 | RNF128 | chrX | 106721701 | 106802016 |
g0015 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RNF128_chrX_106721701_106802016 | RNF128 | chrX | 106721701 | 106802016 |
g0016 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | RNF128_chrX_106721701_106802016 | RNF128 | chrX | 106721701 | 106802016 |
g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF128_chrX_106721701_106802016 | RNF128 | chrX | 106721701 | 106802016 |
g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF128_chrX_106721701_106802016 | RNF128 | chrX | 106721701 | 106802016 |
g0019 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF128_chrX_106721701_106802016 | RNF128 | chrX | 106721701 | 106802016 |
g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF128_chrX_106721701_106802016 | RNF128 | chrX | 106721701 | 106802016 |
g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF128_chrX_106721701_106802016 | RNF128 | chrX | 106721701 | 106802016 |
g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF128_chrX_106721701_106802016 | RNF128 | chrX | 106721701 | 106802016 |
g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF128_chrX_106721701_106802016 | RNF128 | chrX | 106721701 | 106802016 |
g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF128_chrX_106721701_106802016 | RNF128 | chrX | 106721701 | 106802016 |
g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF128_chrX_106721701_106802016 | RNF128 | chrX | 106721701 | 106802016 |
g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF128_chrX_106721701_106802016 | RNF128 | chrX | 106721701 | 106802016 |
g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF128_chrX_106721701_106802016 | RNF128 | chrX | 106721701 | 106802016 |
g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF128_chrX_106721701_106802016 | RNF128 | chrX | 106721701 | 106802016 |
g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF128_chrX_106721701_106802016 | RNF128 | chrX | 106721701 | 106802016 |
g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF128_chrX_106721701_106802016 | RNF128 | chrX | 106721701 | 106802016 |
g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF128_chrX_106721701_106802016 | RNF128 | chrX | 106721701 | 106802016 |
g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF128_chrX_106721701_106802016 | RNF128 | chrX | 106721701 | 106802016 |
g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF128_chrX_106721701_106802016 | RNF128 | chrX | 106721701 | 106802016 |
g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF128_chrX_106721701_106802016 | RNF128 | chrX | 106721701 | 106802016 |
g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF128_chrX_106721701_106802016 | RNF128 | chrX | 106721701 | 106802016 |
g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF128_chrX_106721701_106802016 | RNF128 | chrX | 106721701 | 106802016 |
g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF128_chrX_106721701_106802016 | RNF128 | chrX | 106721701 | 106802016 |
g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF128_chrX_106721701_106802016 | RNF128 | chrX | 106721701 | 106802016 |
g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF128_chrX_106721701_106802016 | RNF128 | chrX | 106721701 | 106802016 |
g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF128_chrX_106721701_106802016 | RNF128 | chrX | 106721701 | 106802016 |
g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF128_chrX_106721701_106802016 | RNF128 | chrX | 106721701 | 106802016 |
g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF128_chrX_106721701_106802016 | RNF128 | chrX | 106721701 | 106802016 |
g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF128_chrX_106721701_106802016 | RNF128 | chrX | 106721701 | 106802016 |
g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF128_chrX_106721701_106802016 | RNF128 | chrX | 106721701 | 106802016 |
g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF128_chrX_106721701_106802016 | RNF128 | chrX | 106721701 | 106802016 |
g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF128_chrX_106721701_106802016 | RNF128 | chrX | 106721701 | 106802016 |
g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF128_chrX_106721701_106802016 | RNF128 | chrX | 106721701 | 106802016 |
g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF128_chrX_106721701_106802016 | RNF128 | chrX | 106721701 | 106802016 |
g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF128_chrX_106721701_106802016 | RNF128 | chrX | 106721701 | 106802016 |
g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF128_chrX_106721701_106802016 | RNF128 | chrX | 106721701 | 106802016 |
g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF128_chrX_106721701_106802016 | RNF128 | chrX | 106721701 | 106802016 |
g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF128_chrX_106721701_106802016 | RNF128 | chrX | 106721701 | 106802016 |
g0053 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RNF128_chrX_106721701_106802016 | RNF128 | chrX | 106721701 | 106802016 |
g0054 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF128_chrX_106721701_106802016 | RNF128 | chrX | 106721701 | 106802016 |
g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF128_chrX_106721701_106802016 | RNF128 | chrX | 106721701 | 106802016 |
g0056 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF128_chrX_106721701_106802016 | RNF128 | chrX | 106721701 | 106802016 |
g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF128_chrX_106721701_106802016 | RNF128 | chrX | 106721701 | 106802016 |
g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF128_chrX_106721701_106802016 | RNF128 | chrX | 106721701 | 106802016 |
g0059 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF128_chrX_106721701_106802016 | RNF128 | chrX | 106721701 | 106802016 |
g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF128_chrX_106721701_106802016 | RNF128 | chrX | 106721701 | 106802016 |
g0061 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF128_chrX_106721701_106802016 | RNF128 | chrX | 106721701 | 106802016 |
g0062 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF128_chrX_106721701_106802016 | RNF128 | chrX | 106721701 | 106802016 |
g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF128_chrX_106721701_106802016 | RNF128 | chrX | 106721701 | 106802016 |
g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF128_chrX_106721701_106802016 | RNF128 | chrX | 106721701 | 106802016 |
g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF128_chrX_106721701_106802016 | RNF128 | chrX | 106721701 | 106802016 |
g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF128_chrX_106721701_106802016 | RNF128 | chrX | 106721701 | 106802016 |
g0067 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF128_chrX_106721701_106802016 | RNF128 | chrX | 106721701 | 106802016 |
g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF128_chrX_106721701_106802016 | RNF128 | chrX | 106721701 | 106802016 |
g0069 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF128_chrX_106721701_106802016 | RNF128 | chrX | 106721701 | 106802016 |
g0070 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF128_chrX_106721701_106802016 | RNF128 | chrX | 106721701 | 106802016 |
g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF128_chrX_106721701_106802016 | RNF128 | chrX | 106721701 | 106802016 |
g0072 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF128_chrX_106721701_106802016 | RNF128 | chrX | 106721701 | 106802016 |
g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF128_chrX_106721701_106802016 | RNF128 | chrX | 106721701 | 106802016 |
g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF128_chrX_106721701_106802016 | RNF128 | chrX | 106721701 | 106802016 |
g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF128_chrX_106721701_106802016 | RNF128 | chrX | 106721701 | 106802016 |
g0076 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF128_chrX_106721701_106802016 | RNF128 | chrX | 106721701 | 106802016 |
g0077 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF128_chrX_106721701_106802016 | RNF128 | chrX | 106721701 | 106802016 |
g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF128_chrX_106721701_106802016 | RNF128 | chrX | 106721701 | 106802016 |
g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF128_chrX_106721701_106802016 | RNF128 | chrX | 106721701 | 106802016 |
g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF128_chrX_106721701_106802016 | RNF128 | chrX | 106721701 | 106802016 |
g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF128_chrX_106721701_106802016 | RNF128 | chrX | 106721701 | 106802016 |
g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF128_chrX_106721701_106802016 | RNF128 | chrX | 106721701 | 106802016 |
g0083 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF128_chrX_106721701_106802016 | RNF128 | chrX | 106721701 | 106802016 |
g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF128_chrX_106721701_106802016 | RNF128 | chrX | 106721701 | 106802016 |
g0085 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RNF128_chrX_106721701_106802016 | RNF128 | chrX | 106721701 | 106802016 |
g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF128_chrX_106721701_106802016 | RNF128 | chrX | 106721701 | 106802016 |
g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF128_chrX_106721701_106802016 | RNF128 | chrX | 106721701 | 106802016 |
g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF128_chrX_106721701_106802016 | RNF128 | chrX | 106721701 | 106802016 |
g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF128_chrX_106721701_106802016 | RNF128 | chrX | 106721701 | 106802016 |
g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF128_chrX_106721701_106802016 | RNF128 | chrX | 106721701 | 106802016 |
g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF128_chrX_106721701_106802016 | RNF128 | chrX | 106721701 | 106802016 |
g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF128_chrX_106721701_106802016 | RNF128 | chrX | 106721701 | 106802016 |
g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF128_chrX_106721701_106802016 | RNF128 | chrX | 106721701 | 106802016 |
g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF128_chrX_106721701_106802016 | RNF128 | chrX | 106721701 | 106802016 |
g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF128_chrX_106721701_106802016 | RNF128 | chrX | 106721701 | 106802016 |
g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF128_chrX_106721701_106802016 | RNF128 | chrX | 106721701 | 106802016 |
g0097 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RNF128_chrX_106721701_106802016 | RNF128 | chrX | 106721701 | 106802016 |
g0098 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF128_chrX_106721701_106802016 | RNF128 | chrX | 106721701 | 106802016 |
g0099 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF128_chrX_106721701_106802016 | RNF128 | chrX | 106721701 | 106802016 |
g0100 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF128_chrX_106721701_106802016 | RNF128 | chrX | 106721701 | 106802016 |
g0101 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RNF128_chrX_106721701_106802016 | RNF128 | chrX | 106721701 | 106802016 |
g0102 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | RNF128_chrX_106721701_106802016 | RNF128 | chrX | 106721701 | 106802016 |
g0103 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF128_chrX_106721701_106802016 | RNF128 | chrX | 106721701 | 106802016 |
g0104 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF128_chrX_106721701_106802016 | RNF128 | chrX | 106721701 | 106802016 |
g0105 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF128_chrX_106721701_106802016 | RNF128 | chrX | 106721701 | 106802016 |
g0106 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF128_chrX_106721701_106802016 | RNF128 | chrX | 106721701 | 106802016 |
g0107 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF128_chrX_106721701_106802016 | RNF128 | chrX | 106721701 | 106802016 |
g0108 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF128_chrX_106721701_106802016 | RNF128 | chrX | 106721701 | 106802016 |
g0109 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF128_chrX_106721701_106802016 | RNF128 | chrX | 106721701 | 106802016 |
g0110 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF128_chrX_106721701_106802016 | RNF128 | chrX | 106721701 | 106802016 |
g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF128_chrX_106721701_106802016 | RNF128 | chrX | 106721701 | 106802016 |
g0112 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF128_chrX_106721701_106802016 | RNF128 | chrX | 106721701 | 106802016 |
g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF128_chrX_106721701_106802016 | RNF128 | chrX | 106721701 | 106802016 |
g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF128_chrX_106721701_106802016 | RNF128 | chrX | 106721701 | 106802016 |
g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF128_chrX_106721701_106802016 | RNF128 | chrX | 106721701 | 106802016 |
g0116 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF128_chrX_106721701_106802016 | RNF128 | chrX | 106721701 | 106802016 |
g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF128_chrX_106721701_106802016 | RNF128 | chrX | 106721701 | 106802016 |
g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF128_chrX_106721701_106802016 | RNF128 | chrX | 106721701 | 106802016 |
g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF128_chrX_106721701_106802016 | RNF128 | chrX | 106721701 | 106802016 |
g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF128_chrX_106721701_106802016 | RNF128 | chrX | 106721701 | 106802016 |
g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF128_chrX_106721701_106802016 | RNF128 | chrX | 106721701 | 106802016 |
g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF128_chrX_106721701_106802016 | RNF128 | chrX | 106721701 | 106802016 |
g0123 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF128_chrX_106721701_106802016 | RNF128 | chrX | 106721701 | 106802016 |
g0124 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF128_chrX_106721701_106802016 | RNF128 | chrX | 106721701 | 106802016 |
g0125 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF128_chrX_106721701_106802016 | RNF128 | chrX | 106721701 | 106802016 |
g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF128_chrX_106721701_106802016 | RNF128 | chrX | 106721701 | 106802016 |
g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF128_chrX_106721701_106802016 | RNF128 | chrX | 106721701 | 106802016 |
g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF128_chrX_106721701_106802016 | RNF128 | chrX | 106721701 | 106802016 |
g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF128_chrX_106721701_106802016 | RNF128 | chrX | 106721701 | 106802016 |
g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF128_chrX_106721701_106802016 | RNF128 | chrX | 106721701 | 106802016 |
g0131 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF128_chrX_106721701_106802016 | RNF128 | chrX | 106721701 | 106802016 |
g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF128_chrX_106721701_106802016 | RNF128 | chrX | 106721701 | 106802016 |
g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF128_chrX_106721701_106802016 | RNF128 | chrX | 106721701 | 106802016 |
g0134 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF128_chrX_106721701_106802016 | RNF128 | chrX | 106721701 | 106802016 |
g0135 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF128_chrX_106721701_106802016 | RNF128 | chrX | 106721701 | 106802016 |
g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF128_chrX_106721701_106802016 | RNF128 | chrX | 106721701 | 106802016 |
g0137 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF128_chrX_106721701_106802016 | RNF128 | chrX | 106721701 | 106802016 |
g0138 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RNF128_chrX_106721701_106802016 | RNF128 | chrX | 106721701 | 106802016 |
g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF128_chrX_106721701_106802016 | RNF128 | chrX | 106721701 | 106802016 |
g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF128_chrX_106721701_106802016 | RNF128 | chrX | 106721701 | 106802016 |
g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF128_chrX_106721701_106802016 | RNF128 | chrX | 106721701 | 106802016 |
g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF128_chrX_106721701_106802016 | RNF128 | chrX | 106721701 | 106802016 |
g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF128_chrX_106721701_106802016 | RNF128 | chrX | 106721701 | 106802016 |
g0144 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF128_chrX_106721701_106802016 | RNF128 | chrX | 106721701 | 106802016 |
g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF128_chrX_106721701_106802016 | RNF128 | chrX | 106721701 | 106802016 |
g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF128_chrX_106721701_106802016 | RNF128 | chrX | 106721701 | 106802016 |
g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF128_chrX_106721701_106802016 | RNF128 | chrX | 106721701 | 106802016 |
g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF128_chrX_106721701_106802016 | RNF128 | chrX | 106721701 | 106802016 |
g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF128_chrX_106721701_106802016 | RNF128 | chrX | 106721701 | 106802016 |
g0150 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF128_chrX_106721701_106802016 | RNF128 | chrX | 106721701 | 106802016 |
g0151 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF128_chrX_106721701_106802016 | RNF128 | chrX | 106721701 | 106802016 |
g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF128_chrX_106721701_106802016 | RNF128 | chrX | 106721701 | 106802016 |
g0153 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF128_chrX_106721701_106802016 | RNF128 | chrX | 106721701 | 106802016 |
g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF128_chrX_106721701_106802016 | RNF128 | chrX | 106721701 | 106802016 |
g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF128_chrX_106721701_106802016 | RNF128 | chrX | 106721701 | 106802016 |
g0156 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF128_chrX_106721701_106802016 | RNF128 | chrX | 106721701 | 106802016 |
g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF128_chrX_106721701_106802016 | RNF128 | chrX | 106721701 | 106802016 |
g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF128_chrX_106721701_106802016 | RNF128 | chrX | 106721701 | 106802016 |
g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF128_chrX_106721701_106802016 | RNF128 | chrX | 106721701 | 106802016 |
g0160 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF128_chrX_106721701_106802016 | RNF128 | chrX | 106721701 | 106802016 |
g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF128_chrX_106721701_106802016 | RNF128 | chrX | 106721701 | 106802016 |
g0162 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF128_chrX_106721701_106802016 | RNF128 | chrX | 106721701 | 106802016 |
g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF128_chrX_106721701_106802016 | RNF128 | chrX | 106721701 | 106802016 |
g0164 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF128_chrX_106721701_106802016 | RNF128 | chrX | 106721701 | 106802016 |
g0165 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RNF128_chrX_106721701_106802016 | RNF128 | chrX | 106721701 | 106802016 |
g0166 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF128_chrX_106721701_106802016 | RNF128 | chrX | 106721701 | 106802016 |
g0167 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF128_chrX_106721701_106802016 | RNF128 | chrX | 106721701 | 106802016 |
g0168 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | RNF128_chrX_106721701_106802016 | RNF128 | chrX | 106721701 | 106802016 |
g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF128_chrX_106721701_106802016 | RNF128 | chrX | 106721701 | 106802016 |
g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF128_chrX_106721701_106802016 | RNF128 | chrX | 106721701 | 106802016 |
g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF128_chrX_106721701_106802016 | RNF128 | chrX | 106721701 | 106802016 |
g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF128_chrX_106721701_106802016 | RNF128 | chrX | 106721701 | 106802016 |
g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF128_chrX_106721701_106802016 | RNF128 | chrX | 106721701 | 106802016 |
g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF128_chrX_106721701_106802016 | RNF128 | chrX | 106721701 | 106802016 |
g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF128_chrX_106721701_106802016 | RNF128 | chrX | 106721701 | 106802016 |
g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF128_chrX_106721701_106802016 | RNF128 | chrX | 106721701 | 106802016 |
g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF128_chrX_106721701_106802016 | RNF128 | chrX | 106721701 | 106802016 |
g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF128_chrX_106721701_106802016 | RNF128 | chrX | 106721701 | 106802016 |
g0179 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF128_chrX_106721701_106802016 | RNF128 | chrX | 106721701 | 106802016 |
g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF128_chrX_106721701_106802016 | RNF128 | chrX | 106721701 | 106802016 |
g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF128_chrX_106721701_106802016 | RNF128 | chrX | 106721701 | 106802016 |
g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF128_chrX_106721701_106802016 | RNF128 | chrX | 106721701 | 106802016 |
g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF128_chrX_106721701_106802016 | RNF128 | chrX | 106721701 | 106802016 |
g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF128_chrX_106721701_106802016 | RNF128 | chrX | 106721701 | 106802016 |
g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF128_chrX_106721701_106802016 | RNF128 | chrX | 106721701 | 106802016 |
g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF128_chrX_106721701_106802016 | RNF128 | chrX | 106721701 | 106802016 |
g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF128_chrX_106721701_106802016 | RNF128 | chrX | 106721701 | 106802016 |
g0188 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF128_chrX_106721701_106802016 | RNF128 | chrX | 106721701 | 106802016 |
achapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 1/1 | 1287 | 207 | 64 | 41 | 73 | 7 | 20 | RNF128_chrX_106721701_106802016 | RNF128 | copy fasta | chrX | 106721701 | 106802016 |
a0002c0002 | 0/0 | 1287 | 1 | 0 | 0 | 1 | 0 | 0 | RNF128_chrX_106721701_106802016 | RNF128 | copy fasta | chrX | 106721701 | 106802016 |
a0003c0003 | 0/0 | 1287 | 1 | 0 | 0 | 1 | 0 | 0 | RNF128_chrX_106721701_106802016 | RNF128 | copy fasta | chrX | 106721701 | 106802016 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 1/1 | 2803 | 181 | 47 | 40 | 66 | 7 | 19 | RNF128_chrX_106721701_106802016 | RNF128 | copy fasta | chrX | 106721701 | 106802016 |
a0001c0001t0002 | 0/0 | 2803 | 17 | 16 | 1 | 0 | 0 | 0 | RNF128_chrX_106721701_106802016 | RNF128 | copy fasta | chrX | 106721701 | 106802016 |
a0001c0001t0003 | 0/0 | 2803 | 5 | 0 | 0 | 5 | 0 | 0 | RNF128_chrX_106721701_106802016 | RNF128 | copy fasta | chrX | 106721701 | 106802016 |
a0001c0001t0004 | 0/0 | 2802 | 1 | 0 | 0 | 1 | 0 | 0 | RNF128_chrX_106721701_106802016 | RNF128 | copy fasta | chrX | 106721701 | 106802016 |
a0001c0001t0005 | 0/0 | 2803 | 1 | 1 | 0 | 0 | 0 | 0 | RNF128_chrX_106721701_106802016 | RNF128 | copy fasta | chrX | 106721701 | 106802016 |
a0001c0001t0006 | 0/0 | 2803 | 1 | 0 | 0 | 0 | 0 | 1 | RNF128_chrX_106721701_106802016 | RNF128 | copy fasta | chrX | 106721701 | 106802016 |
a0001c0001t0007 | 0/0 | 2802 | 1 | 0 | 0 | 1 | 0 | 0 | RNF128_chrX_106721701_106802016 | RNF128 | copy fasta | chrX | 106721701 | 106802016 |
a0002c0002t0001 | 0/0 | 2803 | 1 | 0 | 0 | 1 | 0 | 0 | RNF128_chrX_106721701_106802016 | RNF128 | copy fasta | chrX | 106721701 | 106802016 |
a0003c0003t0003 | 0/0 | 2803 | 1 | 0 | 0 | 1 | 0 | 0 | RNF128_chrX_106721701_106802016 | RNF128 | copy fasta | chrX | 106721701 | 106802016 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0001 | 0/0 | 6 | 1 | 0 | 5 | 0 | 0 | RNF128_chrX_106721701_106802016 | RNF128 | chrX | 106721701 | 106802016 |
a0001c0001t0001g0003 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | RNF128_chrX_106721701_106802016 | RNF128 | chrX | 106721701 | 106802016 |
a0001c0001t0001g0005 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | RNF128_chrX_106721701_106802016 | RNF128 | chrX | 106721701 | 106802016 |
a0001c0001t0001g0006 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | RNF128_chrX_106721701_106802016 | RNF128 | chrX | 106721701 | 106802016 |
a0001c0001t0001g0007 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RNF128_chrX_106721701_106802016 | RNF128 | chrX | 106721701 | 106802016 |
a0001c0001t0001g0008 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RNF128_chrX_106721701_106802016 | RNF128 | chrX | 106721701 | 106802016 |
a0001c0001t0001g0009 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | RNF128_chrX_106721701_106802016 | RNF128 | chrX | 106721701 | 106802016 |
a0001c0001t0001g0010 | 0/0 | 2 | 1 | 0 | 0 | 1 | 0 | RNF128_chrX_106721701_106802016 | RNF128 | chrX | 106721701 | 106802016 |
a0001c0001t0001g0011 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | RNF128_chrX_106721701_106802016 | RNF128 | chrX | 106721701 | 106802016 |
a0001c0001t0001g0012 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RNF128_chrX_106721701_106802016 | RNF128 | chrX | 106721701 | 106802016 |
a0001c0001t0001g0013 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | RNF128_chrX_106721701_106802016 | RNF128 | chrX | 106721701 | 106802016 |
a0001c0001t0001g0014 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | RNF128_chrX_106721701_106802016 | RNF128 | chrX | 106721701 | 106802016 |
a0001c0001t0001g0016 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | RNF128_chrX_106721701_106802016 | RNF128 | chrX | 106721701 | 106802016 |
a0001c0001t0001g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF128_chrX_106721701_106802016 | RNF128 | chrX | 106721701 | 106802016 |
a0001c0001t0001g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF128_chrX_106721701_106802016 | RNF128 | chrX | 106721701 | 106802016 |
a0001c0001t0001g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF128_chrX_106721701_106802016 | RNF128 | chrX | 106721701 | 106802016 |
a0001c0001t0001g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF128_chrX_106721701_106802016 | RNF128 | chrX | 106721701 | 106802016 |
a0001c0001t0001g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF128_chrX_106721701_106802016 | RNF128 | chrX | 106721701 | 106802016 |
a0001c0001t0001g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF128_chrX_106721701_106802016 | RNF128 | chrX | 106721701 | 106802016 |
a0001c0001t0001g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF128_chrX_106721701_106802016 | RNF128 | chrX | 106721701 | 106802016 |
a0001c0001t0001g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF128_chrX_106721701_106802016 | RNF128 | chrX | 106721701 | 106802016 |
a0001c0001t0001g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF128_chrX_106721701_106802016 | RNF128 | chrX | 106721701 | 106802016 |
a0001c0001t0001g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF128_chrX_106721701_106802016 | RNF128 | chrX | 106721701 | 106802016 |
a0001c0001t0001g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF128_chrX_106721701_106802016 | RNF128 | chrX | 106721701 | 106802016 |
a0001c0001t0001g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF128_chrX_106721701_106802016 | RNF128 | chrX | 106721701 | 106802016 |
a0001c0001t0001g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF128_chrX_106721701_106802016 | RNF128 | chrX | 106721701 | 106802016 |
a0001c0001t0001g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF128_chrX_106721701_106802016 | RNF128 | chrX | 106721701 | 106802016 |
a0001c0001t0001g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF128_chrX_106721701_106802016 | RNF128 | chrX | 106721701 | 106802016 |
a0001c0001t0001g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF128_chrX_106721701_106802016 | RNF128 | chrX | 106721701 | 106802016 |
a0001c0001t0001g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF128_chrX_106721701_106802016 | RNF128 | chrX | 106721701 | 106802016 |
a0001c0001t0001g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF128_chrX_106721701_106802016 | RNF128 | chrX | 106721701 | 106802016 |
a0001c0001t0001g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF128_chrX_106721701_106802016 | RNF128 | chrX | 106721701 | 106802016 |
a0001c0001t0001g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF128_chrX_106721701_106802016 | RNF128 | chrX | 106721701 | 106802016 |
a0001c0001t0001g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF128_chrX_106721701_106802016 | RNF128 | chrX | 106721701 | 106802016 |
a0001c0001t0001g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF128_chrX_106721701_106802016 | RNF128 | chrX | 106721701 | 106802016 |
a0001c0001t0001g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF128_chrX_106721701_106802016 | RNF128 | chrX | 106721701 | 106802016 |
a0001c0001t0001g0053 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RNF128_chrX_106721701_106802016 | RNF128 | chrX | 106721701 | 106802016 |
a0001c0001t0001g0054 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF128_chrX_106721701_106802016 | RNF128 | chrX | 106721701 | 106802016 |
a0001c0001t0001g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF128_chrX_106721701_106802016 | RNF128 | chrX | 106721701 | 106802016 |
a0001c0001t0001g0056 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF128_chrX_106721701_106802016 | RNF128 | chrX | 106721701 | 106802016 |
a0001c0001t0001g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF128_chrX_106721701_106802016 | RNF128 | chrX | 106721701 | 106802016 |
a0001c0001t0001g0059 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF128_chrX_106721701_106802016 | RNF128 | chrX | 106721701 | 106802016 |
a0001c0001t0001g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF128_chrX_106721701_106802016 | RNF128 | chrX | 106721701 | 106802016 |
a0001c0001t0001g0061 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF128_chrX_106721701_106802016 | RNF128 | chrX | 106721701 | 106802016 |
a0001c0001t0001g0062 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF128_chrX_106721701_106802016 | RNF128 | chrX | 106721701 | 106802016 |
a0001c0001t0001g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF128_chrX_106721701_106802016 | RNF128 | chrX | 106721701 | 106802016 |
a0001c0001t0001g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF128_chrX_106721701_106802016 | RNF128 | chrX | 106721701 | 106802016 |
a0001c0001t0001g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF128_chrX_106721701_106802016 | RNF128 | chrX | 106721701 | 106802016 |
a0001c0001t0001g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF128_chrX_106721701_106802016 | RNF128 | chrX | 106721701 | 106802016 |
a0001c0001t0001g0067 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF128_chrX_106721701_106802016 | RNF128 | chrX | 106721701 | 106802016 |
a0001c0001t0001g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF128_chrX_106721701_106802016 | RNF128 | chrX | 106721701 | 106802016 |
a0001c0001t0001g0069 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF128_chrX_106721701_106802016 | RNF128 | chrX | 106721701 | 106802016 |
a0001c0001t0001g0070 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF128_chrX_106721701_106802016 | RNF128 | chrX | 106721701 | 106802016 |
a0001c0001t0001g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF128_chrX_106721701_106802016 | RNF128 | chrX | 106721701 | 106802016 |
a0001c0001t0001g0072 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF128_chrX_106721701_106802016 | RNF128 | chrX | 106721701 | 106802016 |
a0001c0001t0001g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF128_chrX_106721701_106802016 | RNF128 | chrX | 106721701 | 106802016 |
a0001c0001t0001g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF128_chrX_106721701_106802016 | RNF128 | chrX | 106721701 | 106802016 |
a0001c0001t0001g0076 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF128_chrX_106721701_106802016 | RNF128 | chrX | 106721701 | 106802016 |
a0001c0001t0001g0077 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF128_chrX_106721701_106802016 | RNF128 | chrX | 106721701 | 106802016 |
a0001c0001t0001g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF128_chrX_106721701_106802016 | RNF128 | chrX | 106721701 | 106802016 |
a0001c0001t0001g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF128_chrX_106721701_106802016 | RNF128 | chrX | 106721701 | 106802016 |
a0001c0001t0001g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF128_chrX_106721701_106802016 | RNF128 | chrX | 106721701 | 106802016 |
a0001c0001t0001g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF128_chrX_106721701_106802016 | RNF128 | chrX | 106721701 | 106802016 |
a0001c0001t0001g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF128_chrX_106721701_106802016 | RNF128 | chrX | 106721701 | 106802016 |
a0001c0001t0001g0083 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF128_chrX_106721701_106802016 | RNF128 | chrX | 106721701 | 106802016 |
a0001c0001t0001g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF128_chrX_106721701_106802016 | RNF128 | chrX | 106721701 | 106802016 |
a0001c0001t0001g0085 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RNF128_chrX_106721701_106802016 | RNF128 | chrX | 106721701 | 106802016 |
a0001c0001t0001g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF128_chrX_106721701_106802016 | RNF128 | chrX | 106721701 | 106802016 |
a0001c0001t0001g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF128_chrX_106721701_106802016 | RNF128 | chrX | 106721701 | 106802016 |
a0001c0001t0001g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF128_chrX_106721701_106802016 | RNF128 | chrX | 106721701 | 106802016 |
a0001c0001t0001g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF128_chrX_106721701_106802016 | RNF128 | chrX | 106721701 | 106802016 |
a0001c0001t0001g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF128_chrX_106721701_106802016 | RNF128 | chrX | 106721701 | 106802016 |
a0001c0001t0001g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF128_chrX_106721701_106802016 | RNF128 | chrX | 106721701 | 106802016 |
a0001c0001t0001g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF128_chrX_106721701_106802016 | RNF128 | chrX | 106721701 | 106802016 |
a0001c0001t0001g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF128_chrX_106721701_106802016 | RNF128 | chrX | 106721701 | 106802016 |
a0001c0001t0001g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF128_chrX_106721701_106802016 | RNF128 | chrX | 106721701 | 106802016 |
a0001c0001t0001g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF128_chrX_106721701_106802016 | RNF128 | chrX | 106721701 | 106802016 |
a0001c0001t0001g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF128_chrX_106721701_106802016 | RNF128 | chrX | 106721701 | 106802016 |
a0001c0001t0001g0097 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RNF128_chrX_106721701_106802016 | RNF128 | chrX | 106721701 | 106802016 |
a0001c0001t0001g0098 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF128_chrX_106721701_106802016 | RNF128 | chrX | 106721701 | 106802016 |
a0001c0001t0001g0099 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF128_chrX_106721701_106802016 | RNF128 | chrX | 106721701 | 106802016 |
a0001c0001t0001g0100 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF128_chrX_106721701_106802016 | RNF128 | chrX | 106721701 | 106802016 |
a0001c0001t0001g0101 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RNF128_chrX_106721701_106802016 | RNF128 | chrX | 106721701 | 106802016 |
a0001c0001t0001g0102 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | RNF128_chrX_106721701_106802016 | RNF128 | chrX | 106721701 | 106802016 |
a0001c0001t0001g0103 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF128_chrX_106721701_106802016 | RNF128 | chrX | 106721701 | 106802016 |
a0001c0001t0001g0104 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF128_chrX_106721701_106802016 | RNF128 | chrX | 106721701 | 106802016 |
a0001c0001t0001g0105 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF128_chrX_106721701_106802016 | RNF128 | chrX | 106721701 | 106802016 |
a0001c0001t0001g0106 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF128_chrX_106721701_106802016 | RNF128 | chrX | 106721701 | 106802016 |
a0001c0001t0001g0107 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF128_chrX_106721701_106802016 | RNF128 | chrX | 106721701 | 106802016 |
a0001c0001t0001g0108 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF128_chrX_106721701_106802016 | RNF128 | chrX | 106721701 | 106802016 |
a0001c0001t0001g0109 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF128_chrX_106721701_106802016 | RNF128 | chrX | 106721701 | 106802016 |
a0001c0001t0001g0110 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF128_chrX_106721701_106802016 | RNF128 | chrX | 106721701 | 106802016 |
a0001c0001t0001g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF128_chrX_106721701_106802016 | RNF128 | chrX | 106721701 | 106802016 |
a0001c0001t0001g0112 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF128_chrX_106721701_106802016 | RNF128 | chrX | 106721701 | 106802016 |
a0001c0001t0001g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF128_chrX_106721701_106802016 | RNF128 | chrX | 106721701 | 106802016 |
a0001c0001t0001g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF128_chrX_106721701_106802016 | RNF128 | chrX | 106721701 | 106802016 |
a0001c0001t0001g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF128_chrX_106721701_106802016 | RNF128 | chrX | 106721701 | 106802016 |
a0001c0001t0001g0116 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF128_chrX_106721701_106802016 | RNF128 | chrX | 106721701 | 106802016 |
a0001c0001t0001g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF128_chrX_106721701_106802016 | RNF128 | chrX | 106721701 | 106802016 |
a0001c0001t0001g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF128_chrX_106721701_106802016 | RNF128 | chrX | 106721701 | 106802016 |
a0001c0001t0001g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF128_chrX_106721701_106802016 | RNF128 | chrX | 106721701 | 106802016 |
a0001c0001t0001g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF128_chrX_106721701_106802016 | RNF128 | chrX | 106721701 | 106802016 |
a0001c0001t0001g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF128_chrX_106721701_106802016 | RNF128 | chrX | 106721701 | 106802016 |
a0001c0001t0001g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF128_chrX_106721701_106802016 | RNF128 | chrX | 106721701 | 106802016 |
a0001c0001t0001g0123 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF128_chrX_106721701_106802016 | RNF128 | chrX | 106721701 | 106802016 |
a0001c0001t0001g0124 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF128_chrX_106721701_106802016 | RNF128 | chrX | 106721701 | 106802016 |
a0001c0001t0001g0125 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF128_chrX_106721701_106802016 | RNF128 | chrX | 106721701 | 106802016 |
a0001c0001t0001g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF128_chrX_106721701_106802016 | RNF128 | chrX | 106721701 | 106802016 |
a0001c0001t0001g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF128_chrX_106721701_106802016 | RNF128 | chrX | 106721701 | 106802016 |
a0001c0001t0001g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF128_chrX_106721701_106802016 | RNF128 | chrX | 106721701 | 106802016 |
a0001c0001t0001g0131 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF128_chrX_106721701_106802016 | RNF128 | chrX | 106721701 | 106802016 |
a0001c0001t0001g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF128_chrX_106721701_106802016 | RNF128 | chrX | 106721701 | 106802016 |
a0001c0001t0001g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF128_chrX_106721701_106802016 | RNF128 | chrX | 106721701 | 106802016 |
a0001c0001t0001g0134 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF128_chrX_106721701_106802016 | RNF128 | chrX | 106721701 | 106802016 |
a0001c0001t0001g0135 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF128_chrX_106721701_106802016 | RNF128 | chrX | 106721701 | 106802016 |
a0001c0001t0001g0137 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF128_chrX_106721701_106802016 | RNF128 | chrX | 106721701 | 106802016 |
a0001c0001t0001g0138 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RNF128_chrX_106721701_106802016 | RNF128 | chrX | 106721701 | 106802016 |
a0001c0001t0001g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF128_chrX_106721701_106802016 | RNF128 | chrX | 106721701 | 106802016 |
a0001c0001t0001g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF128_chrX_106721701_106802016 | RNF128 | chrX | 106721701 | 106802016 |
a0001c0001t0001g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF128_chrX_106721701_106802016 | RNF128 | chrX | 106721701 | 106802016 |
a0001c0001t0001g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF128_chrX_106721701_106802016 | RNF128 | chrX | 106721701 | 106802016 |
a0001c0001t0001g0144 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF128_chrX_106721701_106802016 | RNF128 | chrX | 106721701 | 106802016 |
a0001c0001t0001g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF128_chrX_106721701_106802016 | RNF128 | chrX | 106721701 | 106802016 |
a0001c0001t0001g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF128_chrX_106721701_106802016 | RNF128 | chrX | 106721701 | 106802016 |
a0001c0001t0001g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF128_chrX_106721701_106802016 | RNF128 | chrX | 106721701 | 106802016 |
a0001c0001t0001g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF128_chrX_106721701_106802016 | RNF128 | chrX | 106721701 | 106802016 |
a0001c0001t0001g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF128_chrX_106721701_106802016 | RNF128 | chrX | 106721701 | 106802016 |
a0001c0001t0001g0150 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF128_chrX_106721701_106802016 | RNF128 | chrX | 106721701 | 106802016 |
a0001c0001t0001g0151 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF128_chrX_106721701_106802016 | RNF128 | chrX | 106721701 | 106802016 |
a0001c0001t0001g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF128_chrX_106721701_106802016 | RNF128 | chrX | 106721701 | 106802016 |
a0001c0001t0001g0153 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF128_chrX_106721701_106802016 | RNF128 | chrX | 106721701 | 106802016 |
a0001c0001t0001g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF128_chrX_106721701_106802016 | RNF128 | chrX | 106721701 | 106802016 |
a0001c0001t0001g0156 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF128_chrX_106721701_106802016 | RNF128 | chrX | 106721701 | 106802016 |
a0001c0001t0001g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF128_chrX_106721701_106802016 | RNF128 | chrX | 106721701 | 106802016 |
a0001c0001t0001g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF128_chrX_106721701_106802016 | RNF128 | chrX | 106721701 | 106802016 |
a0001c0001t0001g0160 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF128_chrX_106721701_106802016 | RNF128 | chrX | 106721701 | 106802016 |
a0001c0001t0001g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF128_chrX_106721701_106802016 | RNF128 | chrX | 106721701 | 106802016 |
a0001c0001t0001g0162 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF128_chrX_106721701_106802016 | RNF128 | chrX | 106721701 | 106802016 |
a0001c0001t0001g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF128_chrX_106721701_106802016 | RNF128 | chrX | 106721701 | 106802016 |
a0001c0001t0001g0164 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF128_chrX_106721701_106802016 | RNF128 | chrX | 106721701 | 106802016 |
a0001c0001t0001g0165 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | RNF128_chrX_106721701_106802016 | RNF128 | chrX | 106721701 | 106802016 |
a0001c0001t0001g0166 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF128_chrX_106721701_106802016 | RNF128 | chrX | 106721701 | 106802016 |
a0001c0001t0001g0167 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF128_chrX_106721701_106802016 | RNF128 | chrX | 106721701 | 106802016 |
a0001c0001t0001g0168 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | RNF128_chrX_106721701_106802016 | RNF128 | chrX | 106721701 | 106802016 |
a0001c0001t0001g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF128_chrX_106721701_106802016 | RNF128 | chrX | 106721701 | 106802016 |
a0001c0001t0001g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF128_chrX_106721701_106802016 | RNF128 | chrX | 106721701 | 106802016 |
a0001c0001t0001g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF128_chrX_106721701_106802016 | RNF128 | chrX | 106721701 | 106802016 |
a0001c0001t0001g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF128_chrX_106721701_106802016 | RNF128 | chrX | 106721701 | 106802016 |
a0001c0001t0001g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF128_chrX_106721701_106802016 | RNF128 | chrX | 106721701 | 106802016 |
a0001c0001t0001g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF128_chrX_106721701_106802016 | RNF128 | chrX | 106721701 | 106802016 |
a0001c0001t0001g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF128_chrX_106721701_106802016 | RNF128 | chrX | 106721701 | 106802016 |
a0001c0001t0001g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF128_chrX_106721701_106802016 | RNF128 | chrX | 106721701 | 106802016 |
a0001c0001t0001g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF128_chrX_106721701_106802016 | RNF128 | chrX | 106721701 | 106802016 |
a0001c0001t0001g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF128_chrX_106721701_106802016 | RNF128 | chrX | 106721701 | 106802016 |
a0001c0001t0001g0179 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF128_chrX_106721701_106802016 | RNF128 | chrX | 106721701 | 106802016 |
a0001c0001t0001g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF128_chrX_106721701_106802016 | RNF128 | chrX | 106721701 | 106802016 |
a0001c0001t0001g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF128_chrX_106721701_106802016 | RNF128 | chrX | 106721701 | 106802016 |
a0001c0001t0001g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF128_chrX_106721701_106802016 | RNF128 | chrX | 106721701 | 106802016 |
a0001c0001t0001g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF128_chrX_106721701_106802016 | RNF128 | chrX | 106721701 | 106802016 |
a0001c0001t0001g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF128_chrX_106721701_106802016 | RNF128 | chrX | 106721701 | 106802016 |
a0001c0001t0001g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF128_chrX_106721701_106802016 | RNF128 | chrX | 106721701 | 106802016 |
a0001c0001t0001g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF128_chrX_106721701_106802016 | RNF128 | chrX | 106721701 | 106802016 |
a0001c0001t0001g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF128_chrX_106721701_106802016 | RNF128 | chrX | 106721701 | 106802016 |
a0001c0001t0001g0188 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF128_chrX_106721701_106802016 | RNF128 | chrX | 106721701 | 106802016 |
a0001c0001t0002g0002 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | RNF128_chrX_106721701_106802016 | RNF128 | chrX | 106721701 | 106802016 |
a0001c0001t0002g0004 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | RNF128_chrX_106721701_106802016 | RNF128 | chrX | 106721701 | 106802016 |
a0001c0001t0002g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF128_chrX_106721701_106802016 | RNF128 | chrX | 106721701 | 106802016 |
a0001c0001t0002g0019 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | RNF128_chrX_106721701_106802016 | RNF128 | chrX | 106721701 | 106802016 |
a0001c0001t0002g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF128_chrX_106721701_106802016 | RNF128 | chrX | 106721701 | 106802016 |
a0001c0001t0002g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF128_chrX_106721701_106802016 | RNF128 | chrX | 106721701 | 106802016 |
a0001c0001t0002g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF128_chrX_106721701_106802016 | RNF128 | chrX | 106721701 | 106802016 |
a0001c0001t0002g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF128_chrX_106721701_106802016 | RNF128 | chrX | 106721701 | 106802016 |
a0001c0001t0002g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF128_chrX_106721701_106802016 | RNF128 | chrX | 106721701 | 106802016 |
a0001c0001t0002g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF128_chrX_106721701_106802016 | RNF128 | chrX | 106721701 | 106802016 |
a0001c0001t0002g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF128_chrX_106721701_106802016 | RNF128 | chrX | 106721701 | 106802016 |
a0001c0001t0002g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF128_chrX_106721701_106802016 | RNF128 | chrX | 106721701 | 106802016 |
a0001c0001t0002g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF128_chrX_106721701_106802016 | RNF128 | chrX | 106721701 | 106802016 |
a0001c0001t0002g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF128_chrX_106721701_106802016 | RNF128 | chrX | 106721701 | 106802016 |
a0001c0001t0002g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF128_chrX_106721701_106802016 | RNF128 | chrX | 106721701 | 106802016 |
a0001c0001t0003g0015 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF128_chrX_106721701_106802016 | RNF128 | chrX | 106721701 | 106802016 |
a0001c0001t0003g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF128_chrX_106721701_106802016 | RNF128 | chrX | 106721701 | 106802016 |
a0001c0001t0003g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF128_chrX_106721701_106802016 | RNF128 | chrX | 106721701 | 106802016 |
a0001c0001t0003g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF128_chrX_106721701_106802016 | RNF128 | chrX | 106721701 | 106802016 |
a0001c0001t0003g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF128_chrX_106721701_106802016 | RNF128 | chrX | 106721701 | 106802016 |
a0001c0001t0004g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF128_chrX_106721701_106802016 | RNF128 | chrX | 106721701 | 106802016 |
a0001c0001t0005g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | RNF128_chrX_106721701_106802016 | RNF128 | chrX | 106721701 | 106802016 |
a0001c0001t0006g0001 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | RNF128_chrX_106721701_106802016 | RNF128 | chrX | 106721701 | 106802016 |
a0001c0001t0007g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF128_chrX_106721701_106802016 | RNF128 | chrX | 106721701 | 106802016 |
a0002c0002t0001g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF128_chrX_106721701_106802016 | RNF128 | chrX | 106721701 | 106802016 |
a0003c0003t0003g0015 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | RNF128_chrX_106721701_106802016 | RNF128 | chrX | 106721701 | 106802016 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00140 | hp1 | a0001 | c0001 | t0001 | g0085 | EUR | GBR | RNF128_chrX_106721701_106802016 | RNF128 | chrX | 106721701 | 106802016 |
HG00280 | hp1 | a0001 | c0001 | t0001 | g0010 | EUR | FIN | RNF128_chrX_106721701_106802016 | RNF128 | chrX | 106721701 | 106802016 |
HG00438 | hp1 | a0001 | c0001 | t0001 | g0074 | EAS | CHS | RNF128_chrX_106721701_106802016 | RNF128 | chrX | 106721701 | 106802016 |
HG00438 | hp2 | a0001 | c0001 | t0001 | g0111 | EAS | CHS | RNF128_chrX_106721701_106802016 | RNF128 | chrX | 106721701 | 106802016 |
HG00558 | hp1 | a0001 | c0001 | t0001 | g0172 | EAS | CHS | RNF128_chrX_106721701_106802016 | RNF128 | chrX | 106721701 | 106802016 |
HG00558 | hp2 | a0002 | c0002 | t0001 | g0058 | EAS | CHS | RNF128_chrX_106721701_106802016 | RNF128 | chrX | 106721701 | 106802016 |
HG00609 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | CHS | RNF128_chrX_106721701_106802016 | RNF128 | chrX | 106721701 | 106802016 |
HG00621 | hp1 | a0001 | c0001 | t0001 | g0126 | EAS | CHS | RNF128_chrX_106721701_106802016 | RNF128 | chrX | 106721701 | 106802016 |
HG00642 | hp1 | a0001 | c0001 | t0001 | g0005 | AMR | PUR | RNF128_chrX_106721701_106802016 | RNF128 | chrX | 106721701 | 106802016 |
HG00673 | hp1 | a0001 | c0001 | t0001 | g0055 | EAS | CHS | RNF128_chrX_106721701_106802016 | RNF128 | chrX | 106721701 | 106802016 |
HG00735 | hp1 | a0001 | c0001 | t0001 | g0103 | AMR | PUR | RNF128_chrX_106721701_106802016 | RNF128 | chrX | 106721701 | 106802016 |
HG00735 | hp2 | a0001 | c0001 | t0001 | g0162 | AMR | PUR | RNF128_chrX_106721701_106802016 | RNF128 | chrX | 106721701 | 106802016 |
HG00738 | hp1 | a0001 | c0001 | t0001 | g0112 | AMR | PUR | RNF128_chrX_106721701_106802016 | RNF128 | chrX | 106721701 | 106802016 |
HG00741 | hp1 | a0001 | c0001 | t0001 | g0106 | AMR | PUR | RNF128_chrX_106721701_106802016 | RNF128 | chrX | 106721701 | 106802016 |
HG00741 | hp2 | a0001 | c0001 | t0001 | g0098 | AMR | PUR | RNF128_chrX_106721701_106802016 | RNF128 | chrX | 106721701 | 106802016 |
HG01069 | hp1 | a0001 | c0001 | t0001 | g0016 | AMR | PUR | RNF128_chrX_106721701_106802016 | RNF128 | chrX | 106721701 | 106802016 |
HG01071 | hp1 | a0001 | c0001 | t0001 | g0016 | AMR | PUR | RNF128_chrX_106721701_106802016 | RNF128 | chrX | 106721701 | 106802016 |
HG01071 | hp2 | a0001 | c0001 | t0001 | g0110 | AMR | PUR | RNF128_chrX_106721701_106802016 | RNF128 | chrX | 106721701 | 106802016 |
HG01074 | hp1 | a0001 | c0001 | t0001 | g0061 | AMR | PUR | RNF128_chrX_106721701_106802016 | RNF128 | chrX | 106721701 | 106802016 |
HG01081 | hp1 | a0001 | c0001 | t0001 | g0065 | AMR | PUR | RNF128_chrX_106721701_106802016 | RNF128 | chrX | 106721701 | 106802016 |
HG01081 | hp2 | a0001 | c0001 | t0001 | g0109 | AMR | PUR | RNF128_chrX_106721701_106802016 | RNF128 | chrX | 106721701 | 106802016 |
HG01099 | hp1 | a0001 | c0001 | t0001 | g0124 | AMR | PUR | RNF128_chrX_106721701_106802016 | RNF128 | chrX | 106721701 | 106802016 |
HG01106 | hp1 | a0001 | c0001 | t0001 | g0005 | AMR | PUR | RNF128_chrX_106721701_106802016 | RNF128 | chrX | 106721701 | 106802016 |
HG01109 | hp1 | a0001 | c0001 | t0001 | g0179 | AMR | PUR | RNF128_chrX_106721701_106802016 | RNF128 | chrX | 106721701 | 106802016 |
HG01167 | hp1 | a0001 | c0001 | t0001 | g0011 | AMR | PUR | RNF128_chrX_106721701_106802016 | RNF128 | chrX | 106721701 | 106802016 |
HG01168 | hp1 | a0001 | c0001 | t0001 | g0096 | AMR | PUR | RNF128_chrX_106721701_106802016 | RNF128 | chrX | 106721701 | 106802016 |
HG01168 | hp2 | a0001 | c0001 | t0001 | g0073 | AMR | PUR | RNF128_chrX_106721701_106802016 | RNF128 | chrX | 106721701 | 106802016 |
HG01169 | hp1 | a0001 | c0001 | t0001 | g0011 | AMR | PUR | RNF128_chrX_106721701_106802016 | RNF128 | chrX | 106721701 | 106802016 |
HG01169 | hp2 | a0001 | c0001 | t0001 | g0062 | AMR | PUR | RNF128_chrX_106721701_106802016 | RNF128 | chrX | 106721701 | 106802016 |
HG01175 | hp1 | a0001 | c0001 | t0001 | g0070 | AMR | PUR | RNF128_chrX_106721701_106802016 | RNF128 | chrX | 106721701 | 106802016 |
HG01175 | hp2 | a0001 | c0001 | t0001 | g0164 | AMR | PUR | RNF128_chrX_106721701_106802016 | RNF128 | chrX | 106721701 | 106802016 |
HG01192 | hp1 | a0001 | c0001 | t0001 | g0134 | AMR | PUR | RNF128_chrX_106721701_106802016 | RNF128 | chrX | 106721701 | 106802016 |
HG01243 | hp1 | a0001 | c0001 | t0002 | g0019 | AMR | PUR | RNF128_chrX_106721701_106802016 | RNF128 | chrX | 106721701 | 106802016 |
HG01255 | hp1 | a0001 | c0001 | t0001 | g0104 | AMR | CLM | RNF128_chrX_106721701_106802016 | RNF128 | chrX | 106721701 | 106802016 |
HG01256 | hp1 | a0001 | c0001 | t0001 | g0067 | AMR | CLM | RNF128_chrX_106721701_106802016 | RNF128 | chrX | 106721701 | 106802016 |
HG01257 | hp1 | a0001 | c0001 | t0001 | g0072 | AMR | CLM | RNF128_chrX_106721701_106802016 | RNF128 | chrX | 106721701 | 106802016 |
HG01257 | hp2 | a0001 | c0001 | t0001 | g0105 | AMR | CLM | RNF128_chrX_106721701_106802016 | RNF128 | chrX | 106721701 | 106802016 |
HG01258 | hp1 | a0001 | c0001 | t0001 | g0082 | AMR | CLM | RNF128_chrX_106721701_106802016 | RNF128 | chrX | 106721701 | 106802016 |
HG01261 | hp1 | a0001 | c0001 | t0001 | g0069 | AMR | CLM | RNF128_chrX_106721701_106802016 | RNF128 | chrX | 106721701 | 106802016 |
HG01358 | hp1 | a0001 | c0001 | t0001 | g0166 | AMR | CLM | RNF128_chrX_106721701_106802016 | RNF128 | chrX | 106721701 | 106802016 |
HG01433 | hp1 | a0001 | c0001 | t0001 | g0151 | AMR | CLM | RNF128_chrX_106721701_106802016 | RNF128 | chrX | 106721701 | 106802016 |
HG01515 | hp1 | a0001 | c0001 | t0001 | g0097 | EUR | IBS | RNF128_chrX_106721701_106802016 | RNF128 | chrX | 106721701 | 106802016 |
HG01516 | hp1 | a0001 | c0001 | t0001 | g0101 | EUR | IBS | RNF128_chrX_106721701_106802016 | RNF128 | chrX | 106721701 | 106802016 |
HG01516 | hp2 | a0001 | c0001 | t0001 | g0053 | EUR | IBS | RNF128_chrX_106721701_106802016 | RNF128 | chrX | 106721701 | 106802016 |
HG01884 | hp1 | a0001 | c0001 | t0001 | g0152 | AFR | ACB | RNF128_chrX_106721701_106802016 | RNF128 | chrX | 106721701 | 106802016 |
HG01884 | hp2 | a0001 | c0001 | t0002 | g0024 | AFR | ACB | RNF128_chrX_106721701_106802016 | RNF128 | chrX | 106721701 | 106802016 |
HG01928 | hp1 | a0001 | c0001 | t0001 | g0077 | AMR | PEL | RNF128_chrX_106721701_106802016 | RNF128 | chrX | 106721701 | 106802016 |
HG01934 | hp1 | a0001 | c0001 | t0001 | g0014 | AMR | PEL | RNF128_chrX_106721701_106802016 | RNF128 | chrX | 106721701 | 106802016 |
HG01943 | hp1 | a0001 | c0001 | t0001 | g0059 | AMR | PEL | RNF128_chrX_106721701_106802016 | RNF128 | chrX | 106721701 | 106802016 |
HG01952 | hp1 | a0001 | c0001 | t0001 | g0160 | AMR | PEL | RNF128_chrX_106721701_106802016 | RNF128 | chrX | 106721701 | 106802016 |
HG01981 | hp1 | a0001 | c0001 | t0001 | g0167 | AMR | PEL | RNF128_chrX_106721701_106802016 | RNF128 | chrX | 106721701 | 106802016 |
HG01981 | hp2 | a0001 | c0001 | t0001 | g0083 | AMR | PEL | RNF128_chrX_106721701_106802016 | RNF128 | chrX | 106721701 | 106802016 |
HG02015 | hp1 | a0001 | c0001 | t0001 | g0086 | EAS | KHV | RNF128_chrX_106721701_106802016 | RNF128 | chrX | 106721701 | 106802016 |
HG02027 | hp1 | a0001 | c0001 | t0001 | g0088 | EAS | KHV | RNF128_chrX_106721701_106802016 | RNF128 | chrX | 106721701 | 106802016 |
HG02040 | hp1 | a0001 | c0001 | t0001 | g0146 | EAS | KHV | RNF128_chrX_106721701_106802016 | RNF128 | chrX | 106721701 | 106802016 |
HG02055 | hp1 | a0001 | c0001 | t0001 | g0081 | AFR | ACB | RNF128_chrX_106721701_106802016 | RNF128 | chrX | 106721701 | 106802016 |
HG02056 | hp1 | a0001 | c0001 | t0001 | g0122 | EAS | KHV | RNF128_chrX_106721701_106802016 | RNF128 | chrX | 106721701 | 106802016 |
HG02071 | hp1 | a0001 | c0001 | t0001 | g0095 | EAS | KHV | RNF128_chrX_106721701_106802016 | RNF128 | chrX | 106721701 | 106802016 |
HG02074 | hp1 | a0001 | c0001 | t0001 | g0007 | EAS | KHV | RNF128_chrX_106721701_106802016 | RNF128 | chrX | 106721701 | 106802016 |
HG02080 | hp1 | a0001 | c0001 | t0001 | g0087 | EAS | KHV | RNF128_chrX_106721701_106802016 | RNF128 | chrX | 106721701 | 106802016 |
HG02080 | hp2 | a0001 | c0001 | t0001 | g0090 | EAS | KHV | RNF128_chrX_106721701_106802016 | RNF128 | chrX | 106721701 | 106802016 |
HG02083 | hp1 | a0001 | c0001 | t0001 | g0171 | EAS | KHV | RNF128_chrX_106721701_106802016 | RNF128 | chrX | 106721701 | 106802016 |
HG02129 | hp1 | a0001 | c0001 | t0001 | g0113 | EAS | KHV | RNF128_chrX_106721701_106802016 | RNF128 | chrX | 106721701 | 106802016 |
HG02132 | hp1 | a0001 | c0001 | t0001 | g0007 | EAS | KHV | RNF128_chrX_106721701_106802016 | RNF128 | chrX | 106721701 | 106802016 |
HG02135 | hp1 | a0003 | c0003 | t0003 | g0015 | EAS | KHV | RNF128_chrX_106721701_106802016 | RNF128 | chrX | 106721701 | 106802016 |
HG02145 | hp1 | a0001 | c0001 | t0002 | g0026 | AFR | ACB | RNF128_chrX_106721701_106802016 | RNF128 | chrX | 106721701 | 106802016 |
HG02155 | hp1 | a0001 | c0001 | t0001 | g0121 | EAS | CDX | RNF128_chrX_106721701_106802016 | RNF128 | chrX | 106721701 | 106802016 |
HG02155 | hp2 | a0001 | c0001 | t0001 | g0064 | EAS | CDX | RNF128_chrX_106721701_106802016 | RNF128 | chrX | 106721701 | 106802016 |
HG02258 | hp1 | a0001 | c0001 | t0001 | g0187 | AFR | ACB | RNF128_chrX_106721701_106802016 | RNF128 | chrX | 106721701 | 106802016 |
HG02293 | hp1 | a0001 | c0001 | t0001 | g0144 | AMR | PEL | RNF128_chrX_106721701_106802016 | RNF128 | chrX | 106721701 | 106802016 |
HG02293 | hp2 | a0001 | c0001 | t0001 | g0108 | AMR | PEL | RNF128_chrX_106721701_106802016 | RNF128 | chrX | 106721701 | 106802016 |
HG02300 | hp1 | a0001 | c0001 | t0001 | g0131 | AMR | PEL | RNF128_chrX_106721701_106802016 | RNF128 | chrX | 106721701 | 106802016 |
HG02572 | hp1 | a0001 | c0001 | t0001 | g0027 | AFR | GWD | RNF128_chrX_106721701_106802016 | RNF128 | chrX | 106721701 | 106802016 |
HG02602 | hp1 | a0001 | c0001 | t0001 | g0135 | SAS | PJL | RNF128_chrX_106721701_106802016 | RNF128 | chrX | 106721701 | 106802016 |
HG02622 | hp1 | a0001 | c0001 | t0001 | g0182 | AFR | GWD | RNF128_chrX_106721701_106802016 | RNF128 | chrX | 106721701 | 106802016 |
HG02622 | hp2 | a0001 | c0001 | t0002 | g0154 | AFR | GWD | RNF128_chrX_106721701_106802016 | RNF128 | chrX | 106721701 | 106802016 |
HG02630 | hp1 | a0001 | c0001 | t0001 | g0003 | AFR | GWD | RNF128_chrX_106721701_106802016 | RNF128 | chrX | 106721701 | 106802016 |
HG02630 | hp2 | a0001 | c0001 | t0002 | g0004 | AFR | GWD | RNF128_chrX_106721701_106802016 | RNF128 | chrX | 106721701 | 106802016 |
HG02647 | hp1 | a0001 | c0001 | t0001 | g0048 | AFR | GWD | RNF128_chrX_106721701_106802016 | RNF128 | chrX | 106721701 | 106802016 |
HG02698 | hp1 | a0001 | c0001 | t0001 | g0116 | SAS | PJL | RNF128_chrX_106721701_106802016 | RNF128 | chrX | 106721701 | 106802016 |
HG02717 | hp1 | a0001 | c0001 | t0001 | g0046 | AFR | GWD | RNF128_chrX_106721701_106802016 | RNF128 | chrX | 106721701 | 106802016 |
HG02723 | hp1 | a0001 | c0001 | t0001 | g0033 | AFR | GWD | RNF128_chrX_106721701_106802016 | RNF128 | chrX | 106721701 | 106802016 |
HG02723 | hp2 | a0001 | c0001 | t0001 | g0071 | AFR | GWD | RNF128_chrX_106721701_106802016 | RNF128 | chrX | 106721701 | 106802016 |
HG02735 | hp1 | a0001 | c0001 | t0001 | g0150 | SAS | PJL | RNF128_chrX_106721701_106802016 | RNF128 | chrX | 106721701 | 106802016 |
HG02738 | hp1 | a0001 | c0001 | t0001 | g0156 | SAS | PJL | RNF128_chrX_106721701_106802016 | RNF128 | chrX | 106721701 | 106802016 |
HG02809 | hp1 | a0001 | c0001 | t0002 | g0041 | AFR | GWD | RNF128_chrX_106721701_106802016 | RNF128 | chrX | 106721701 | 106802016 |
HG02809 | hp2 | a0001 | c0001 | t0001 | g0029 | AFR | GWD | RNF128_chrX_106721701_106802016 | RNF128 | chrX | 106721701 | 106802016 |
HG02818 | hp1 | a0001 | c0001 | t0001 | g0003 | AFR | GWD | RNF128_chrX_106721701_106802016 | RNF128 | chrX | 106721701 | 106802016 |
HG02818 | hp2 | a0001 | c0001 | t0002 | g0044 | AFR | GWD | RNF128_chrX_106721701_106802016 | RNF128 | chrX | 106721701 | 106802016 |
HG02886 | hp1 | a0001 | c0001 | t0001 | g0036 | AFR | GWD | RNF128_chrX_106721701_106802016 | RNF128 | chrX | 106721701 | 106802016 |
HG02886 | hp2 | a0001 | c0001 | t0001 | g0176 | AFR | GWD | RNF128_chrX_106721701_106802016 | RNF128 | chrX | 106721701 | 106802016 |
HG02895 | hp1 | a0001 | c0001 | t0002 | g0002 | AFR | GWD | RNF128_chrX_106721701_106802016 | RNF128 | chrX | 106721701 | 106802016 |
HG02897 | hp1 | a0001 | c0001 | t0001 | g0183 | AFR | GWD | RNF128_chrX_106721701_106802016 | RNF128 | chrX | 106721701 | 106802016 |
HG02897 | hp2 | a0001 | c0001 | t0002 | g0002 | AFR | GWD | RNF128_chrX_106721701_106802016 | RNF128 | chrX | 106721701 | 106802016 |
HG02922 | hp1 | a0001 | c0001 | t0001 | g0035 | AFR | ESN | RNF128_chrX_106721701_106802016 | RNF128 | chrX | 106721701 | 106802016 |
HG02922 | hp2 | a0001 | c0001 | t0005 | g0052 | AFR | ESN | RNF128_chrX_106721701_106802016 | RNF128 | chrX | 106721701 | 106802016 |
HG02965 | hp1 | a0001 | c0001 | t0001 | g0169 | AFR | ESN | RNF128_chrX_106721701_106802016 | RNF128 | chrX | 106721701 | 106802016 |
HG02976 | hp1 | a0001 | c0001 | t0001 | g0186 | AFR | ESN | RNF128_chrX_106721701_106802016 | RNF128 | chrX | 106721701 | 106802016 |
HG02976 | hp2 | a0001 | c0001 | t0001 | g0181 | AFR | ESN | RNF128_chrX_106721701_106802016 | RNF128 | chrX | 106721701 | 106802016 |
HG03017 | hp1 | a0001 | c0001 | t0001 | g0123 | SAS | PJL | RNF128_chrX_106721701_106802016 | RNF128 | chrX | 106721701 | 106802016 |
HG03041 | hp1 | a0001 | c0001 | t0001 | g0084 | AFR | GWD | RNF128_chrX_106721701_106802016 | RNF128 | chrX | 106721701 | 106802016 |
HG03041 | hp2 | a0001 | c0001 | t0001 | g0148 | AFR | GWD | RNF128_chrX_106721701_106802016 | RNF128 | chrX | 106721701 | 106802016 |
HG03098 | hp1 | a0001 | c0001 | t0001 | g0185 | AFR | MSL | RNF128_chrX_106721701_106802016 | RNF128 | chrX | 106721701 | 106802016 |
HG03130 | hp1 | a0001 | c0001 | t0001 | g0039 | AFR | ESN | RNF128_chrX_106721701_106802016 | RNF128 | chrX | 106721701 | 106802016 |
HG03139 | hp1 | a0001 | c0001 | t0001 | g0147 | AFR | ESN | RNF128_chrX_106721701_106802016 | RNF128 | chrX | 106721701 | 106802016 |
HG03209 | hp1 | a0001 | c0001 | t0002 | g0004 | AFR | MSL | RNF128_chrX_106721701_106802016 | RNF128 | chrX | 106721701 | 106802016 |
HG03225 | hp1 | a0001 | c0001 | t0001 | g0047 | AFR | MSL | RNF128_chrX_106721701_106802016 | RNF128 | chrX | 106721701 | 106802016 |
HG03453 | hp1 | a0001 | c0001 | t0001 | g0032 | AFR | MSL | RNF128_chrX_106721701_106802016 | RNF128 | chrX | 106721701 | 106802016 |
HG03453 | hp2 | a0001 | c0001 | t0002 | g0043 | AFR | MSL | RNF128_chrX_106721701_106802016 | RNF128 | chrX | 106721701 | 106802016 |
HG03486 | hp1 | a0001 | c0001 | t0001 | g0031 | AFR | MSL | RNF128_chrX_106721701_106802016 | RNF128 | chrX | 106721701 | 106802016 |
HG03486 | hp2 | a0001 | c0001 | t0002 | g0022 | AFR | MSL | RNF128_chrX_106721701_106802016 | RNF128 | chrX | 106721701 | 106802016 |
HG03490 | hp1 | a0001 | c0001 | t0001 | g0137 | SAS | PJL | RNF128_chrX_106721701_106802016 | RNF128 | chrX | 106721701 | 106802016 |
HG03491 | hp1 | a0001 | c0001 | t0001 | g0054 | SAS | PJL | RNF128_chrX_106721701_106802016 | RNF128 | chrX | 106721701 | 106802016 |
HG03491 | hp2 | a0001 | c0001 | t0001 | g0009 | SAS | PJL | RNF128_chrX_106721701_106802016 | RNF128 | chrX | 106721701 | 106802016 |
HG03492 | hp1 | a0001 | c0001 | t0001 | g0009 | SAS | PJL | RNF128_chrX_106721701_106802016 | RNF128 | chrX | 106721701 | 106802016 |
HG03540 | hp1 | a0001 | c0001 | t0001 | g0050 | AFR | GWD | RNF128_chrX_106721701_106802016 | RNF128 | chrX | 106721701 | 106802016 |
HG03540 | hp2 | a0001 | c0001 | t0002 | g0020 | AFR | GWD | RNF128_chrX_106721701_106802016 | RNF128 | chrX | 106721701 | 106802016 |
HG03579 | hp1 | a0001 | c0001 | t0001 | g0177 | AFR | MSL | RNF128_chrX_106721701_106802016 | RNF128 | chrX | 106721701 | 106802016 |
HG03654 | hp1 | a0001 | c0001 | t0006 | g0001 | SAS | PJL | RNF128_chrX_106721701_106802016 | RNF128 | chrX | 106721701 | 106802016 |
HG03688 | hp1 | a0001 | c0001 | t0001 | g0107 | SAS | STU | RNF128_chrX_106721701_106802016 | RNF128 | chrX | 106721701 | 106802016 |
HG03710 | hp1 | a0001 | c0001 | t0001 | g0153 | SAS | PJL | RNF128_chrX_106721701_106802016 | RNF128 | chrX | 106721701 | 106802016 |
HG03831 | hp1 | a0001 | c0001 | t0001 | g0014 | SAS | BEB | RNF128_chrX_106721701_106802016 | RNF128 | chrX | 106721701 | 106802016 |
HG03831 | hp2 | a0001 | c0001 | t0001 | g0100 | SAS | BEB | RNF128_chrX_106721701_106802016 | RNF128 | chrX | 106721701 | 106802016 |
HG03942 | hp1 | a0001 | c0001 | t0001 | g0188 | SAS | BEB | RNF128_chrX_106721701_106802016 | RNF128 | chrX | 106721701 | 106802016 |
HG04115 | hp1 | a0001 | c0001 | t0001 | g0076 | SAS | STU | RNF128_chrX_106721701_106802016 | RNF128 | chrX | 106721701 | 106802016 |
HG04199 | hp1 | a0001 | c0001 | t0001 | g0006 | SAS | STU | RNF128_chrX_106721701_106802016 | RNF128 | chrX | 106721701 | 106802016 |
HG04204 | hp1 | a0001 | c0001 | t0001 | g0099 | SAS | STU | RNF128_chrX_106721701_106802016 | RNF128 | chrX | 106721701 | 106802016 |
HG04228 | hp1 | a0001 | c0001 | t0001 | g0056 | SAS | STU | RNF128_chrX_106721701_106802016 | RNF128 | chrX | 106721701 | 106802016 |
NA18522 | hp1 | a0001 | c0001 | t0002 | g0023 | AFR | YRI | RNF128_chrX_106721701_106802016 | RNF128 | chrX | 106721701 | 106802016 |
NA18612 | hp1 | a0001 | c0001 | t0001 | g0063 | EAS | CHB | RNF128_chrX_106721701_106802016 | RNF128 | chrX | 106721701 | 106802016 |
NA18747 | hp1 | a0001 | c0001 | t0001 | g0139 | EAS | CHB | RNF128_chrX_106721701_106802016 | RNF128 | chrX | 106721701 | 106802016 |
NA18906 | hp1 | a0001 | c0001 | t0001 | g0180 | AFR | YRI | RNF128_chrX_106721701_106802016 | RNF128 | chrX | 106721701 | 106802016 |
NA18906 | hp2 | a0001 | c0001 | t0001 | g0045 | AFR | YRI | RNF128_chrX_106721701_106802016 | RNF128 | chrX | 106721701 | 106802016 |
NA18940 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | RNF128_chrX_106721701_106802016 | RNF128 | chrX | 106721701 | 106802016 |
NA18943 | hp1 | a0001 | c0001 | t0001 | g0092 | EAS | JPT | RNF128_chrX_106721701_106802016 | RNF128 | chrX | 106721701 | 106802016 |
NA18944 | hp1 | a0001 | c0001 | t0001 | g0078 | EAS | JPT | RNF128_chrX_106721701_106802016 | RNF128 | chrX | 106721701 | 106802016 |
NA18945 | hp1 | a0001 | c0001 | t0001 | g0115 | EAS | JPT | RNF128_chrX_106721701_106802016 | RNF128 | chrX | 106721701 | 106802016 |
NA18948 | hp1 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | RNF128_chrX_106721701_106802016 | RNF128 | chrX | 106721701 | 106802016 |
NA18950 | hp1 | a0001 | c0001 | t0001 | g0149 | EAS | JPT | RNF128_chrX_106721701_106802016 | RNF128 | chrX | 106721701 | 106802016 |
NA18950 | hp2 | a0001 | c0001 | t0001 | g0057 | EAS | JPT | RNF128_chrX_106721701_106802016 | RNF128 | chrX | 106721701 | 106802016 |
NA18952 | hp1 | a0001 | c0001 | t0001 | g0089 | EAS | JPT | RNF128_chrX_106721701_106802016 | RNF128 | chrX | 106721701 | 106802016 |
NA18953 | hp1 | a0001 | c0001 | t0001 | g0114 | EAS | JPT | RNF128_chrX_106721701_106802016 | RNF128 | chrX | 106721701 | 106802016 |
NA18959 | hp1 | a0001 | c0001 | t0001 | g0093 | EAS | JPT | RNF128_chrX_106721701_106802016 | RNF128 | chrX | 106721701 | 106802016 |
NA18960 | hp1 | a0001 | c0001 | t0001 | g0133 | EAS | JPT | RNF128_chrX_106721701_106802016 | RNF128 | chrX | 106721701 | 106802016 |
NA18961 | hp1 | a0001 | c0001 | t0001 | g0060 | EAS | JPT | RNF128_chrX_106721701_106802016 | RNF128 | chrX | 106721701 | 106802016 |
NA18962 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | RNF128_chrX_106721701_106802016 | RNF128 | chrX | 106721701 | 106802016 |
NA18965 | hp1 | a0001 | c0001 | t0001 | g0119 | EAS | JPT | RNF128_chrX_106721701_106802016 | RNF128 | chrX | 106721701 | 106802016 |
NA18966 | hp1 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | RNF128_chrX_106721701_106802016 | RNF128 | chrX | 106721701 | 106802016 |
NA18970 | hp1 | a0001 | c0001 | t0001 | g0161 | EAS | JPT | RNF128_chrX_106721701_106802016 | RNF128 | chrX | 106721701 | 106802016 |
NA18971 | hp1 | a0001 | c0001 | t0001 | g0132 | EAS | JPT | RNF128_chrX_106721701_106802016 | RNF128 | chrX | 106721701 | 106802016 |
NA18977 | hp1 | a0001 | c0001 | t0001 | g0143 | EAS | JPT | RNF128_chrX_106721701_106802016 | RNF128 | chrX | 106721701 | 106802016 |
NA18982 | hp1 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | RNF128_chrX_106721701_106802016 | RNF128 | chrX | 106721701 | 106802016 |
NA18983 | hp1 | a0001 | c0001 | t0003 | g0130 | EAS | JPT | RNF128_chrX_106721701_106802016 | RNF128 | chrX | 106721701 | 106802016 |
NA18984 | hp1 | a0001 | c0001 | t0003 | g0141 | EAS | JPT | RNF128_chrX_106721701_106802016 | RNF128 | chrX | 106721701 | 106802016 |
NA18986 | hp1 | a0001 | c0001 | t0001 | g0066 | EAS | JPT | RNF128_chrX_106721701_106802016 | RNF128 | chrX | 106721701 | 106802016 |
NA18988 | hp1 | a0001 | c0001 | t0001 | g0068 | EAS | JPT | RNF128_chrX_106721701_106802016 | RNF128 | chrX | 106721701 | 106802016 |
NA18989 | hp1 | a0001 | c0001 | t0007 | g0075 | EAS | JPT | RNF128_chrX_106721701_106802016 | RNF128 | chrX | 106721701 | 106802016 |
NA18990 | hp1 | a0001 | c0001 | t0001 | g0079 | EAS | JPT | RNF128_chrX_106721701_106802016 | RNF128 | chrX | 106721701 | 106802016 |
NA18994 | hp1 | a0001 | c0001 | t0001 | g0051 | EAS | JPT | RNF128_chrX_106721701_106802016 | RNF128 | chrX | 106721701 | 106802016 |
NA18995 | hp1 | a0001 | c0001 | t0003 | g0136 | EAS | JPT | RNF128_chrX_106721701_106802016 | RNF128 | chrX | 106721701 | 106802016 |
NA19000 | hp1 | a0001 | c0001 | t0001 | g0094 | EAS | JPT | RNF128_chrX_106721701_106802016 | RNF128 | chrX | 106721701 | 106802016 |
NA19004 | hp1 | a0001 | c0001 | t0001 | g0080 | EAS | JPT | RNF128_chrX_106721701_106802016 | RNF128 | chrX | 106721701 | 106802016 |
NA19005 | hp1 | a0001 | c0001 | t0001 | g0129 | EAS | JPT | RNF128_chrX_106721701_106802016 | RNF128 | chrX | 106721701 | 106802016 |
NA19006 | hp1 | a0001 | c0001 | t0001 | g0140 | EAS | JPT | RNF128_chrX_106721701_106802016 | RNF128 | chrX | 106721701 | 106802016 |
NA19007 | hp1 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | RNF128_chrX_106721701_106802016 | RNF128 | chrX | 106721701 | 106802016 |
NA19009 | hp1 | a0001 | c0001 | t0001 | g0158 | EAS | JPT | RNF128_chrX_106721701_106802016 | RNF128 | chrX | 106721701 | 106802016 |
NA19012 | hp1 | a0001 | c0001 | t0003 | g0015 | EAS | JPT | RNF128_chrX_106721701_106802016 | RNF128 | chrX | 106721701 | 106802016 |
NA19030 | hp1 | a0001 | c0001 | t0001 | g0028 | AFR | LWK | RNF128_chrX_106721701_106802016 | RNF128 | chrX | 106721701 | 106802016 |
NA19030 | hp2 | a0001 | c0001 | t0001 | g0049 | AFR | LWK | RNF128_chrX_106721701_106802016 | RNF128 | chrX | 106721701 | 106802016 |
NA19043 | hp1 | a0001 | c0001 | t0001 | g0030 | AFR | LWK | RNF128_chrX_106721701_106802016 | RNF128 | chrX | 106721701 | 106802016 |
NA19055 | hp1 | a0001 | c0001 | t0001 | g0145 | EAS | JPT | RNF128_chrX_106721701_106802016 | RNF128 | chrX | 106721701 | 106802016 |
NA19056 | hp1 | a0001 | c0001 | t0001 | g0117 | EAS | JPT | RNF128_chrX_106721701_106802016 | RNF128 | chrX | 106721701 | 106802016 |
NA19058 | hp1 | a0001 | c0001 | t0004 | g0128 | EAS | JPT | RNF128_chrX_106721701_106802016 | RNF128 | chrX | 106721701 | 106802016 |
NA19060 | hp1 | a0001 | c0001 | t0001 | g0170 | EAS | JPT | RNF128_chrX_106721701_106802016 | RNF128 | chrX | 106721701 | 106802016 |
NA19062 | hp1 | a0001 | c0001 | t0001 | g0142 | EAS | JPT | RNF128_chrX_106721701_106802016 | RNF128 | chrX | 106721701 | 106802016 |
NA19063 | hp1 | a0001 | c0001 | t0001 | g0118 | EAS | JPT | RNF128_chrX_106721701_106802016 | RNF128 | chrX | 106721701 | 106802016 |
NA19066 | hp1 | a0001 | c0001 | t0003 | g0159 | EAS | JPT | RNF128_chrX_106721701_106802016 | RNF128 | chrX | 106721701 | 106802016 |
NA19070 | hp1 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | RNF128_chrX_106721701_106802016 | RNF128 | chrX | 106721701 | 106802016 |
NA19072 | hp1 | a0001 | c0001 | t0001 | g0157 | EAS | JPT | RNF128_chrX_106721701_106802016 | RNF128 | chrX | 106721701 | 106802016 |
NA19076 | hp1 | a0001 | c0001 | t0001 | g0127 | EAS | JPT | RNF128_chrX_106721701_106802016 | RNF128 | chrX | 106721701 | 106802016 |
NA19079 | hp1 | a0001 | c0001 | t0001 | g0173 | EAS | JPT | RNF128_chrX_106721701_106802016 | RNF128 | chrX | 106721701 | 106802016 |
NA19082 | hp1 | a0001 | c0001 | t0001 | g0120 | EAS | JPT | RNF128_chrX_106721701_106802016 | RNF128 | chrX | 106721701 | 106802016 |
NA19083 | hp1 | a0001 | c0001 | t0001 | g0163 | EAS | JPT | RNF128_chrX_106721701_106802016 | RNF128 | chrX | 106721701 | 106802016 |
NA19085 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | RNF128_chrX_106721701_106802016 | RNF128 | chrX | 106721701 | 106802016 |
NA19086 | hp1 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | RNF128_chrX_106721701_106802016 | RNF128 | chrX | 106721701 | 106802016 |
NA19088 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | RNF128_chrX_106721701_106802016 | RNF128 | chrX | 106721701 | 106802016 |
NA19091 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | RNF128_chrX_106721701_106802016 | RNF128 | chrX | 106721701 | 106802016 |
NA19240 | hp1 | a0001 | c0001 | t0002 | g0025 | AFR | YRI | RNF128_chrX_106721701_106802016 | RNF128 | chrX | 106721701 | 106802016 |
NA19240 | hp2 | a0001 | c0001 | t0001 | g0174 | AFR | YRI | RNF128_chrX_106721701_106802016 | RNF128 | chrX | 106721701 | 106802016 |
NA20129 | hp1 | a0001 | c0001 | t0001 | g0010 | AFR | ASW | RNF128_chrX_106721701_106802016 | RNF128 | chrX | 106721701 | 106802016 |
NA20129 | hp2 | a0001 | c0001 | t0001 | g0018 | AFR | ASW | RNF128_chrX_106721701_106802016 | RNF128 | chrX | 106721701 | 106802016 |
NA20752 | hp1 | a0001 | c0001 | t0001 | g0138 | EUR | TSI | RNF128_chrX_106721701_106802016 | RNF128 | chrX | 106721701 | 106802016 |
NA20805 | hp1 | a0001 | c0001 | t0001 | g0165 | EUR | TSI | RNF128_chrX_106721701_106802016 | RNF128 | chrX | 106721701 | 106802016 |
NA20905 | hp1 | a0001 | c0001 | t0001 | g0125 | SAS | GIH | RNF128_chrX_106721701_106802016 | RNF128 | chrX | 106721701 | 106802016 |
HG02109 | hp1 | a0001 | c0001 | t0001 | g0038 | AFR | ACB | RNF128_chrX_106721701_106802016 | RNF128 | chrX | 106721701 | 106802016 |
HG02109 | hp2 | a0001 | c0001 | t0001 | g0040 | AFR | ACB | RNF128_chrX_106721701_106802016 | RNF128 | chrX | 106721701 | 106802016 |
HG02486 | hp1 | a0001 | c0001 | t0001 | g0034 | AFR | ACB | RNF128_chrX_106721701_106802016 | RNF128 | chrX | 106721701 | 106802016 |
HG02559 | hp1 | a0001 | c0001 | t0002 | g0017 | AFR | ACB | RNF128_chrX_106721701_106802016 | RNF128 | chrX | 106721701 | 106802016 |
HG02559 | hp2 | a0001 | c0001 | t0001 | g0184 | AFR | ACB | RNF128_chrX_106721701_106802016 | RNF128 | chrX | 106721701 | 106802016 |
HG03471 | hp1 | a0001 | c0001 | t0001 | g0155 | AFR | MSL | RNF128_chrX_106721701_106802016 | RNF128 | chrX | 106721701 | 106802016 |
HG06807 | hp1 | a0001 | c0001 | t0001 | g0037 | AFR | USA | RNF128_chrX_106721701_106802016 | RNF128 | chrX | 106721701 | 106802016 |
HG06807 | hp2 | a0001 | c0001 | t0001 | g0178 | AFR | USA | RNF128_chrX_106721701_106802016 | RNF128 | chrX | 106721701 | 106802016 |
NA18955 | hp1 | a0001 | c0001 | t0001 | g0091 | EAS | JPT | RNF128_chrX_106721701_106802016 | RNF128 | chrX | 106721701 | 106802016 |
NA20300 | hp1 | a0001 | c0001 | t0001 | g0175 | AFR | USA | RNF128_chrX_106721701_106802016 | RNF128 | chrX | 106721701 | 106802016 |
NA20300 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | USA | RNF128_chrX_106721701_106802016 | RNF128 | chrX | 106721701 | 106802016 |
NA21309 | hp1 | a0001 | c0001 | t0001 | g0042 | AFR | LWK | RNF128_chrX_106721701_106802016 | RNF128 | chrX | 106721701 | 106802016 |
NA21309 | hp2 | a0001 | c0001 | t0002 | g0021 | AFR | LWK | RNF128_chrX_106721701_106802016 | RNF128 | chrX | 106721701 | 106802016 |
homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0001 | g0102 | REF | REF | RNF128_chrX_106721701_106802016 | RNF128 | chrX | 106721701 | 106802016 |
homoSapiens_grch38 | hp1 | a0001 | c0001 | t0001 | g0168 | REF | REF | RNF128_chrX_106721701_106802016 | RNF128 | chrX | 106721701 | 106802016 |
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:106791112
|
A | G | 1 | a0003 | 1 | HG02135.hp1 | missense_variant | MODERATE | c.1031A>G | p.Asn344Ser | RNF128 | ENSG00000133135.14 | transcript | ENST00000255499.3 | protein_coding | 6/7 | 1244/2803 | 1031/1287 | 344/428 | chrX | 106791112 | ||
chrX:106791120
|
T | C | 1 | a0002 | 1 | HG00558.hp2 | missense_variant | MODERATE | c.1039T>C | p.Ser347Pro | RNF128 | ENSG00000133135.14 | transcript | ENST00000255499.3 | protein_coding | 6/7 | 1252/2803 | 1039/1287 | 347/428 | chrX | 106791120 |
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 |
---|
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:106726750
|
TG | T | 1 | a0001c0001t0007 | 1 | NA18989.hp1 | 5_prime_UTR_variant | MODIFIER | c.-163delG | RNF128 | ENSG00000133135.14 | transcript | ENST00000255499.3 | protein_coding | 1/7 | 163 | chrX | 106726750 | |||||
chrX:106795744
|
A | G | 1 | a0001c0001t0006 | 1 | HG03654.hp1 | 3_prime_UTR_variant | MODIFIER | c.*31A>G | RNF128 | ENSG00000133135.14 | transcript | ENST00000255499.3 | protein_coding | 7/7 | 31 | chrX | 106795744 | |||||
chrX:106796568
|
A | G | 1 | a0001c0001t0005 | 1 | HG02922.hp2 | 3_prime_UTR_variant | MODIFIER | c.*855A>G | RNF128 | ENSG00000133135.14 | transcript | ENST00000255499.3 | protein_coding | 7/7 | 855 | chrX | 106796568 | |||||
chrX:106796632
|
C | T | 2 | a0001c0001t0003a0003c0003t0003 | 6 | HG02135.hp1 NA18983.hp1 NA18984.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*919C>T | RNF128 | ENSG00000133135.14 | transcript | ENST00000255499.3 | protein_coding | 7/7 | 919 | chrX | 106796632 | |||||
chrX:106796705
|
AG | A | 1 | a0001c0001t0004 | 1 | NA19058.hp1 | 3_prime_UTR_variant | MODIFIER | c.*999delG | RNF128 | ENSG00000133135.14 | transcript | ENST00000255499.3 | protein_coding | 7/7 | 999 | INFO_REALIGN_3_PRIME | chrX | 106796705 | ||||
chrX:106796816
|
T | C | 1 | a0001c0001t0002 | 17 | HG01243.hp1 HG01884.hp2 HG02145.hp1 others(14): Show |
3_prime_UTR_variant | MODIFIER | c.*1103T>C | RNF128 | ENSG00000133135.14 | transcript | ENST00000255499.3 | protein_coding | 7/7 | 1103 | chrX | 106796816 |
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:106727451
|
T | C | 31 | a0001c0001t0001g0003a0001c0001t0001g0018a0001c0001t0001g0027others(28): Show | 34 | HG01243.hp1 HG01884.hp2 HG02109.hp1 others(31): Show |
intron_variant | MODIFIER | c.484+54T>C | RNF128 | ENSG00000133135.14 | transcript | ENST00000255499.3 | protein_coding | 1/6 | chrX | 106727451 | ||||||
chrX:106728086
|
G | GA | 1 | a0001c0001t0002g0002 | 2 | HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.484+698dupA | RNF128 | ENSG00000133135.14 | transcript | ENST00000255499.3 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chrX | 106728086 | |||||
chrX:106728212
|
G | C | 6 | a0001c0001t0001g0045a0001c0001t0001g0046a0001c0001t0001g0047others(3): Show | 6 | HG02647.hp1 HG02717.hp1 HG03225.hp1 others(3): Show |
intron_variant | MODIFIER | c.484+815G>C | RNF128 | ENSG00000133135.14 | transcript | ENST00000255499.3 | protein_coding | 1/6 | chrX | 106728212 | ||||||
chrX:106728281
|
T | C | 1 | a0001c0001t0002g0017 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.484+884T>C | RNF128 | ENSG00000133135.14 | transcript | ENST00000255499.3 | protein_coding | 1/6 | chrX | 106728281 | ||||||
chrX:106728562
|
A | G | 1 | a0001c0001t0002g0044 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.484+1165A>G | RNF128 | ENSG00000133135.14 | transcript | ENST00000255499.3 | protein_coding | 1/6 | chrX | 106728562 | ||||||
chrX:106728912
|
A | G | 1 | a0001c0001t0002g0017 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.484+1515A>G | RNF128 | ENSG00000133135.14 | transcript | ENST00000255499.3 | protein_coding | 1/6 | chrX | 106728912 | ||||||
chrX:106729498
|
G | C | 1 | a0001c0001t0001g0018 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.484+2101G>C | RNF128 | ENSG00000133135.14 | transcript | ENST00000255499.3 | protein_coding | 1/6 | chrX | 106729498 | ||||||
chrX:106729755
|
G | GA | 1 | a0001c0001t0001g0051 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.484+2363dupA | RNF128 | ENSG00000133135.14 | transcript | ENST00000255499.3 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chrX | 106729755 | |||||
chrX:106730052
|
T | C | 1 | a0001c0001t0001g0045 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.484+2655T>C | RNF128 | ENSG00000133135.14 | transcript | ENST00000255499.3 | protein_coding | 1/6 | chrX | 106730052 | ||||||
chrX:106730273
|
ATT | A | 1 | a0001c0001t0005g0052 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.484+2879_484+2880d others(4): Show |
RNF128 | ENSG00000133135.14 | transcript | ENST00000255499.3 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chrX | 106730273 | |||||
chrX:106730668
|
A | G | 31 | a0001c0001t0001g0003a0001c0001t0001g0018a0001c0001t0001g0027others(28): Show | 34 | HG01243.hp1 HG01884.hp2 HG02109.hp1 others(31): Show |
intron_variant | MODIFIER | c.484+3271A>G | RNF128 | ENSG00000133135.14 | transcript | ENST00000255499.3 | protein_coding | 1/6 | chrX | 106730668 | ||||||
chrX:106730746
|
C | T | 1 | a0001c0001t0001g0188 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.484+3349C>T | RNF128 | ENSG00000133135.14 | transcript | ENST00000255499.3 | protein_coding | 1/6 | chrX | 106730746 | ||||||
chrX:106730962
|
T | A | 1 | a0001c0001t0001g0053 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.484+3565T>A | RNF128 | ENSG00000133135.14 | transcript | ENST00000255499.3 | protein_coding | 1/6 | chrX | 106730962 | ||||||
chrX:106732269
|
G | A | 44 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(41): Show | 48 | HG00140.hp1 HG00438.hp1 HG00558.hp2 others(45): Show |
intron_variant | MODIFIER | c.484+4872G>A | RNF128 | ENSG00000133135.14 | transcript | ENST00000255499.3 | protein_coding | 1/6 | chrX | 106732269 | ||||||
chrX:106733006
|
G | A | 1 | a0001c0001t0001g0046 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.484+5609G>A | RNF128 | ENSG00000133135.14 | transcript | ENST00000255499.3 | protein_coding | 1/6 | chrX | 106733006 | ||||||
chrX:106733160
|
G | A | 3 | a0001c0001t0001g0092a0001c0001t0001g0093a0001c0001t0001g0094 | 3 | NA18943.hp1 NA18959.hp1 NA19000.hp1 |
intron_variant | MODIFIER | c.484+5763G>A | RNF128 | ENSG00000133135.14 | transcript | ENST00000255499.3 | protein_coding | 1/6 | chrX | 106733160 | ||||||
chrX:106733228
|
A | G | 2 | a0001c0001t0001g0186a0001c0001t0001g0187 | 2 | HG02258.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.484+5831A>G | RNF128 | ENSG00000133135.14 | transcript | ENST00000255499.3 | protein_coding | 1/6 | chrX | 106733228 | ||||||
chrX:106733345
|
T | C | 1 | a0001c0001t0001g0095 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.484+5948T>C | RNF128 | ENSG00000133135.14 | transcript | ENST00000255499.3 | protein_coding | 1/6 | chrX | 106733345 | ||||||
chrX:106733756
|
C | T | 2 | a0001c0001t0002g0004a0001c0001t0002g0043 | 3 | HG02630.hp2 HG03209.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.484+6359C>T | RNF128 | ENSG00000133135.14 | transcript | ENST00000255499.3 | protein_coding | 1/6 | chrX | 106733756 | ||||||
chrX:106733883
|
C | G | 14 | a0001c0001t0001g0174a0001c0001t0001g0175a0001c0001t0001g0176others(11): Show | 14 | HG01109.hp1 HG02258.hp1 HG02559.hp2 others(11): Show |
intron_variant | MODIFIER | c.484+6486C>G | RNF128 | ENSG00000133135.14 | transcript | ENST00000255499.3 | protein_coding | 1/6 | chrX | 106733883 | ||||||
chrX:106734165
|
TG | T | 1 | a0001c0001t0001g0096 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.484+6772delG | RNF128 | ENSG00000133135.14 | transcript | ENST00000255499.3 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chrX | 106734165 | |||||
chrX:106734259
|
T | C | 1 | a0001c0001t0001g0186 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.484+6862T>C | RNF128 | ENSG00000133135.14 | transcript | ENST00000255499.3 | protein_coding | 1/6 | chrX | 106734259 | ||||||
chrX:106734574
|
A | G | 2 | a0001c0001t0001g0172a0001c0001t0001g0173 | 2 | HG00558.hp1 NA19079.hp1 |
intron_variant | MODIFIER | c.484+7177A>G | RNF128 | ENSG00000133135.14 | transcript | ENST00000255499.3 | protein_coding | 1/6 | chrX | 106734574 | ||||||
chrX:106734727
|
A | G | 2 | a0001c0001t0001g0170a0001c0001t0001g0171 | 2 | HG02083.hp1 NA19060.hp1 |
intron_variant | MODIFIER | c.484+7330A>G | RNF128 | ENSG00000133135.14 | transcript | ENST00000255499.3 | protein_coding | 1/6 | chrX | 106734727 | ||||||
chrX:106735434
|
G | A | 188 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0005others(185): Show | 207 | HG00140.hp1 HG00280.hp1 HG00438.hp1 others(204): Show |
intron_variant | MODIFIER | c.484+8037G>A | RNF128 | ENSG00000133135.14 | transcript | ENST00000255499.3 | protein_coding | 1/6 | chrX | 106735434 | ||||||
chrX:106735482
|
G | T | 1 | a0001c0001t0001g0042 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.484+8085G>T | RNF128 | ENSG00000133135.14 | transcript | ENST00000255499.3 | protein_coding | 1/6 | chrX | 106735482 | ||||||
chrX:106735740
|
A | G | 3 | a0001c0001t0001g0183a0001c0001t0001g0184a0001c0001t0001g0185 | 3 | HG02559.hp2 HG02897.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.484+8343A>G | RNF128 | ENSG00000133135.14 | transcript | ENST00000255499.3 | protein_coding | 1/6 | chrX | 106735740 | ||||||
chrX:106736110
|
A | G | 1 | a0001c0001t0001g0167 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.484+8713A>G | RNF128 | ENSG00000133135.14 | transcript | ENST00000255499.3 | protein_coding | 1/6 | chrX | 106736110 | ||||||
chrX:106736525
|
A | G | 1 | a0001c0001t0002g0041 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.484+9128A>G | RNF128 | ENSG00000133135.14 | transcript | ENST00000255499.3 | protein_coding | 1/6 | chrX | 106736525 | ||||||
chrX:106737082
|
A | T | 1 | a0001c0001t0001g0166 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.484+9685A>T | RNF128 | ENSG00000133135.14 | transcript | ENST00000255499.3 | protein_coding | 1/6 | chrX | 106737082 | ||||||
chrX:106737368
|
C | T | 9 | a0001c0001t0001g0174a0001c0001t0001g0175a0001c0001t0001g0176others(6): Show | 9 | HG01109.hp1 HG02622.hp1 HG02886.hp2 others(6): Show |
intron_variant | MODIFIER | c.484+9971C>T | RNF128 | ENSG00000133135.14 | transcript | ENST00000255499.3 | protein_coding | 1/6 | chrX | 106737368 | ||||||
chrX:106737799
|
C | T | 189 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0005others(186): Show | 208 | HG00140.hp1 HG00280.hp1 HG00438.hp1 others(205): Show |
intron_variant | MODIFIER | c.484+10402C>T | RNF128 | ENSG00000133135.14 | transcript | ENST00000255499.3 | protein_coding | 1/6 | chrX | 106737799 | ||||||
chrX:106738220
|
G | A | 1 | a0001c0001t0001g0054 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.484+10823G>A | RNF128 | ENSG00000133135.14 | transcript | ENST00000255499.3 | protein_coding | 1/6 | chrX | 106738220 | ||||||
chrX:106738226
|
C | G | 2 | a0001c0001t0001g0039a0001c0001t0001g0040 | 2 | HG02109.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.484+10829C>G | RNF128 | ENSG00000133135.14 | transcript | ENST00000255499.3 | protein_coding | 1/6 | chrX | 106738226 | ||||||
chrX:106738280
|
C | T | 45 | a0001c0001t0001g0003a0001c0001t0001g0018a0001c0001t0001g0027others(42): Show | 48 | HG01109.hp1 HG01243.hp1 HG01884.hp2 others(45): Show |
intron_variant | MODIFIER | c.484+10883C>T | RNF128 | ENSG00000133135.14 | transcript | ENST00000255499.3 | protein_coding | 1/6 | chrX | 106738280 | ||||||
chrX:106738334
|
T | C | 1 | a0001c0001t0001g0097 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.484+10937T>C | RNF128 | ENSG00000133135.14 | transcript | ENST00000255499.3 | protein_coding | 1/6 | chrX | 106738334 | ||||||
chrX:106738815
|
AAATT | A | 1 | a0001c0001t0001g0009 | 2 | HG03491.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.484+11421_484+1142 others(8): Show |
RNF128 | ENSG00000133135.14 | transcript | ENST00000255499.3 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chrX | 106738815 | |||||
chrX:106738891
|
C | G | 3 | a0001c0001t0001g0089a0001c0001t0001g0090a0001c0001t0001g0091 | 3 | HG02080.hp2 NA18952.hp1 NA18955.hp1 |
intron_variant | MODIFIER | c.484+11494C>G | RNF128 | ENSG00000133135.14 | transcript | ENST00000255499.3 | protein_coding | 1/6 | chrX | 106738891 | ||||||
chrX:106739033
|
A | G | 1 | a0001c0001t0001g0045 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.484+11636A>G | RNF128 | ENSG00000133135.14 | transcript | ENST00000255499.3 | protein_coding | 1/6 | chrX | 106739033 | ||||||
chrX:106739105
|
C | A | 17 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0011others(14): Show | 20 | HG00280.hp1 HG00735.hp1 HG00741.hp1 others(17): Show |
intron_variant | MODIFIER | c.484+11708C>A | RNF128 | ENSG00000133135.14 | transcript | ENST00000255499.3 | protein_coding | 1/6 | chrX | 106739105 | ||||||
chrX:106739133
|
T | TTTCC | 12 | a0001c0001t0002g0002a0001c0001t0002g0017a0001c0001t0002g0019others(9): Show | 13 | HG01243.hp1 HG01884.hp2 HG02145.hp1 others(10): Show |
intron_variant | MODIFIER | c.484+11756_484+1175 others(8): Show |
RNF128 | ENSG00000133135.14 | transcript | ENST00000255499.3 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chrX | 106739133 | |||||
chrX:106739156
|
C | A | 1 | a0001c0001t0001g0111 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.484+11759C>A | RNF128 | ENSG00000133135.14 | transcript | ENST00000255499.3 | protein_coding | 1/6 | chrX | 106739156 | ||||||
chrX:106739458
|
C | A | 1 | a0001c0001t0002g0017 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.484+12061C>A | RNF128 | ENSG00000133135.14 | transcript | ENST00000255499.3 | protein_coding | 1/6 | chrX | 106739458 | ||||||
chrX:106739688
|
A | T | 31 | a0001c0001t0001g0003a0001c0001t0001g0018a0001c0001t0001g0027others(28): Show | 34 | HG01243.hp1 HG01884.hp2 HG02109.hp1 others(31): Show |
intron_variant | MODIFIER | c.484+12291A>T | RNF128 | ENSG00000133135.14 | transcript | ENST00000255499.3 | protein_coding | 1/6 | chrX | 106739688 | ||||||
chrX:106739827
|
C | T | 1 | a0001c0001t0001g0165 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.484+12430C>T | RNF128 | ENSG00000133135.14 | transcript | ENST00000255499.3 | protein_coding | 1/6 | chrX | 106739827 | ||||||
chrX:106740055
|
G | A | 1 | a0001c0001t0001g0112 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.484+12658G>A | RNF128 | ENSG00000133135.14 | transcript | ENST00000255499.3 | protein_coding | 1/6 | chrX | 106740055 | ||||||
chrX:106740109
|
A | G | 16 | a0001c0001t0001g0003a0001c0001t0001g0018a0001c0001t0001g0027others(13): Show | 17 | HG02109.hp1 HG02109.hp2 HG02486.hp1 others(14): Show |
intron_variant | MODIFIER | c.484+12712A>G | RNF128 | ENSG00000133135.14 | transcript | ENST00000255499.3 | protein_coding | 1/6 | chrX | 106740109 | ||||||
chrX:106740192
|
G | A | 1 | a0001c0001t0001g0113 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.484+12795G>A | RNF128 | ENSG00000133135.14 | transcript | ENST00000255499.3 | protein_coding | 1/6 | chrX | 106740192 | ||||||
chrX:106740203
|
T | G | 1 | a0001c0001t0001g0055 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.484+12806T>G | RNF128 | ENSG00000133135.14 | transcript | ENST00000255499.3 | protein_coding | 1/6 | chrX | 106740203 | ||||||
chrX:106740319
|
T | A | 1 | a0001c0001t0001g0042 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.484+12922T>A | RNF128 | ENSG00000133135.14 | transcript | ENST00000255499.3 | protein_coding | 1/6 | chrX | 106740319 | ||||||
chrX:106740353
|
C | T | 1 | a0001c0001t0001g0164 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.484+12956C>T | RNF128 | ENSG00000133135.14 | transcript | ENST00000255499.3 | protein_coding | 1/6 | chrX | 106740353 | ||||||
chrX:106740513
|
A | G | 3 | a0001c0001t0001g0086a0001c0001t0001g0087a0001c0001t0001g0088 | 3 | HG02015.hp1 HG02027.hp1 HG02080.hp1 |
intron_variant | MODIFIER | c.484+13116A>G | RNF128 | ENSG00000133135.14 | transcript | ENST00000255499.3 | protein_coding | 1/6 | chrX | 106740513 | ||||||
chrX:106740981
|
G | A | 5 | a0001c0001t0001g0003a0001c0001t0001g0018a0001c0001t0001g0027others(2): Show | 6 | HG02572.hp1 HG02630.hp1 HG02809.hp2 others(3): Show |
intron_variant | MODIFIER | c.484+13584G>A | RNF128 | ENSG00000133135.14 | transcript | ENST00000255499.3 | protein_coding | 1/6 | chrX | 106740981 | ||||||
chrX:106741023
|
CATAA | C | 1 | a0001c0001t0002g0041 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.484+13634_484+1363 others(8): Show |
RNF128 | ENSG00000133135.14 | transcript | ENST00000255499.3 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chrX | 106741023 | |||||
chrX:106741140
|
A | G | 1 | a0001c0001t0001g0163 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.484+13743A>G | RNF128 | ENSG00000133135.14 | transcript | ENST00000255499.3 | protein_coding | 1/6 | chrX | 106741140 | ||||||
chrX:106741273
|
A | G | 1 | a0001c0001t0001g0182 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.484+13876A>G | RNF128 | ENSG00000133135.14 | transcript | ENST00000255499.3 | protein_coding | 1/6 | chrX | 106741273 | ||||||
chrX:106741538
|
T | C | 1 | a0001c0001t0001g0056 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.484+14141T>C | RNF128 | ENSG00000133135.14 | transcript | ENST00000255499.3 | protein_coding | 1/6 | chrX | 106741538 | ||||||
chrX:106741556
|
T | G | 2 | a0001c0001t0001g0186a0001c0001t0001g0187 | 2 | HG02258.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.484+14159T>G | RNF128 | ENSG00000133135.14 | transcript | ENST00000255499.3 | protein_coding | 1/6 | chrX | 106741556 | ||||||
chrX:106741947
|
A | T | 1 | a0001c0001t0001g0162 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.484+14550A>T | RNF128 | ENSG00000133135.14 | transcript | ENST00000255499.3 | protein_coding | 1/6 | chrX | 106741947 | ||||||
chrX:106742179
|
A | T | 8 | a0001c0001t0001g0031a0001c0001t0001g0032a0001c0001t0001g0033others(5): Show | 8 | HG02109.hp1 HG02486.hp1 HG02723.hp1 others(5): Show |
intron_variant | MODIFIER | c.484+14782A>T | RNF128 | ENSG00000133135.14 | transcript | ENST00000255499.3 | protein_coding | 1/6 | chrX | 106742179 | ||||||
chrX:106742343
|
C | T | 1 | a0001c0001t0001g0164 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.484+14946C>T | RNF128 | ENSG00000133135.14 | transcript | ENST00000255499.3 | protein_coding | 1/6 | chrX | 106742343 | ||||||
chrX:106742426
|
C | G | 1 | a0001c0001t0001g0161 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.484+15029C>G | RNF128 | ENSG00000133135.14 | transcript | ENST00000255499.3 | protein_coding | 1/6 | chrX | 106742426 | ||||||
chrX:106743093
|
A | G | 1 | a0001c0001t0001g0160 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.484+15696A>G | RNF128 | ENSG00000133135.14 | transcript | ENST00000255499.3 | protein_coding | 1/6 | chrX | 106743093 | ||||||
chrX:106743223
|
G | C | 1 | a0001c0001t0001g0031 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.484+15826G>C | RNF128 | ENSG00000133135.14 | transcript | ENST00000255499.3 | protein_coding | 1/6 | chrX | 106743223 | ||||||
chrX:106743301
|
C | T | 1 | a0001c0001t0003g0159 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.484+15904C>T | RNF128 | ENSG00000133135.14 | transcript | ENST00000255499.3 | protein_coding | 1/6 | chrX | 106743301 | ||||||
chrX:106743327
|
T | A | 1 | a0001c0001t0001g0056 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.484+15930T>A | RNF128 | ENSG00000133135.14 | transcript | ENST00000255499.3 | protein_coding | 1/6 | chrX | 106743327 | ||||||
chrX:106743572
|
C | T | 1 | a0001c0001t0001g0158 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.484+16175C>T | RNF128 | ENSG00000133135.14 | transcript | ENST00000255499.3 | protein_coding | 1/6 | chrX | 106743572 | ||||||
chrX:106743597
|
T | C | 1 | a0001c0001t0001g0098 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.484+16200T>C | RNF128 | ENSG00000133135.14 | transcript | ENST00000255499.3 | protein_coding | 1/6 | chrX | 106743597 | ||||||
chrX:106743803
|
T | C | 45 | a0001c0001t0001g0003a0001c0001t0001g0018a0001c0001t0001g0027others(42): Show | 48 | HG01109.hp1 HG01243.hp1 HG01884.hp2 others(45): Show |
intron_variant | MODIFIER | c.484+16406T>C | RNF128 | ENSG00000133135.14 | transcript | ENST00000255499.3 | protein_coding | 1/6 | chrX | 106743803 | ||||||
chrX:106744477
|
A | AAT | 1 | a0001c0001t0001g0018 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.484+17093_484+1709 others(6): Show |
RNF128 | ENSG00000133135.14 | transcript | ENST00000255499.3 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chrX | 106744477 | |||||
chrX:106744665
|
T | C | 2 | a0001c0001t0001g0114a0001c0001t0001g0115 | 2 | NA18945.hp1 NA18953.hp1 |
intron_variant | MODIFIER | c.484+17268T>C | RNF128 | ENSG00000133135.14 | transcript | ENST00000255499.3 | protein_coding | 1/6 | chrX | 106744665 | ||||||
chrX:106744774
|
T | TA | 1 | a0001c0001t0001g0042 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.484+17378dupA | RNF128 | ENSG00000133135.14 | transcript | ENST00000255499.3 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chrX | 106744774 | |||||
chrX:106744792
|
G | A | 14 | a0001c0001t0001g0174a0001c0001t0001g0175a0001c0001t0001g0176others(11): Show | 14 | HG01109.hp1 HG02258.hp1 HG02559.hp2 others(11): Show |
intron_variant | MODIFIER | c.484+17395G>A | RNF128 | ENSG00000133135.14 | transcript | ENST00000255499.3 | protein_coding | 1/6 | chrX | 106744792 | ||||||
chrX:106744817
|
T | C | 1 | a0001c0001t0001g0116 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.484+17420T>C | RNF128 | ENSG00000133135.14 | transcript | ENST00000255499.3 | protein_coding | 1/6 | chrX | 106744817 | ||||||
chrX:106745317
|
C | T | 1 | a0001c0001t0001g0181 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.484+17920C>T | RNF128 | ENSG00000133135.14 | transcript | ENST00000255499.3 | protein_coding | 1/6 | chrX | 106745317 | ||||||
chrX:106745585
|
G | T | 1 | a0001c0001t0001g0110 | 1 | HG01071.hp2 | intron_variant | MODIFIER | c.484+18188G>T | RNF128 | ENSG00000133135.14 | transcript | ENST00000255499.3 | protein_coding | 1/6 | chrX | 106745585 | ||||||
chrX:106745728
|
C | T | 1 | a0001c0001t0001g0157 | 1 | NA19072.hp1 | intron_variant | MODIFIER | c.484+18331C>T | RNF128 | ENSG00000133135.14 | transcript | ENST00000255499.3 | protein_coding | 1/6 | chrX | 106745728 | ||||||
chrX:106745835
|
AT | A | 1 | a0001c0001t0001g0117 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.484+18448delT | RNF128 | ENSG00000133135.14 | transcript | ENST00000255499.3 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chrX | 106745835 | |||||
chrX:106746208
|
G | A | 3 | a0001c0001t0001g0118a0001c0001t0001g0119a0001c0001t0001g0120 | 3 | NA18965.hp1 NA19063.hp1 NA19082.hp1 |
intron_variant | MODIFIER | c.484+18811G>A | RNF128 | ENSG00000133135.14 | transcript | ENST00000255499.3 | protein_coding | 1/6 | chrX | 106746208 | ||||||
chrX:106746365
|
T | C | 2 | a0001c0001t0001g0114a0001c0001t0001g0115 | 2 | NA18945.hp1 NA18953.hp1 |
intron_variant | MODIFIER | c.484+18968T>C | RNF128 | ENSG00000133135.14 | transcript | ENST00000255499.3 | protein_coding | 1/6 | chrX | 106746365 | ||||||
chrX:106746787
|
A | G | 9 | a0001c0001t0001g0174a0001c0001t0001g0175a0001c0001t0001g0176others(6): Show | 9 | HG01109.hp1 HG02622.hp1 HG02886.hp2 others(6): Show |
intron_variant | MODIFIER | c.484+19390A>G | RNF128 | ENSG00000133135.14 | transcript | ENST00000255499.3 | protein_coding | 1/6 | chrX | 106746787 | ||||||
chrX:106746857
|
C | A | 1 | a0001c0001t0001g0121 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.484+19460C>A | RNF128 | ENSG00000133135.14 | transcript | ENST00000255499.3 | protein_coding | 1/6 | chrX | 106746857 | ||||||
chrX:106746865
|
G | A | 2 | a0001c0001t0001g0057a0002c0002t0001g0058 | 2 | HG00558.hp2 NA18950.hp2 |
intron_variant | MODIFIER | c.484+19468G>A | RNF128 | ENSG00000133135.14 | transcript | ENST00000255499.3 | protein_coding | 1/6 | chrX | 106746865 | ||||||
chrX:106746865
|
GTTA | G | 1 | a0001c0001t0001g0099 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.484+19475_484+1947 others(7): Show |
RNF128 | ENSG00000133135.14 | transcript | ENST00000255499.3 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chrX | 106746865 | |||||
chrX:106746901
|
C | G | 188 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0005others(185): Show | 207 | HG00140.hp1 HG00280.hp1 HG00438.hp1 others(204): Show |
intron_variant | MODIFIER | c.484+19504C>G | RNF128 | ENSG00000133135.14 | transcript | ENST00000255499.3 | protein_coding | 1/6 | chrX | 106746901 | ||||||
chrX:106747043
|
G | A | 1 | a0001c0001t0001g0042 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.484+19646G>A | RNF128 | ENSG00000133135.14 | transcript | ENST00000255499.3 | protein_coding | 1/6 | chrX | 106747043 | ||||||
chrX:106747370
|
G | A | 2 | a0001c0001t0001g0032a0001c0001t0001g0033 | 2 | HG02723.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.484+19973G>A | RNF128 | ENSG00000133135.14 | transcript | ENST00000255499.3 | protein_coding | 1/6 | chrX | 106747370 | ||||||
chrX:106747433
|
G | A | 17 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0011others(14): Show | 20 | HG00280.hp1 HG00735.hp1 HG00741.hp1 others(17): Show |
intron_variant | MODIFIER | c.484+20036G>A | RNF128 | ENSG00000133135.14 | transcript | ENST00000255499.3 | protein_coding | 1/6 | chrX | 106747433 | ||||||
chrX:106747703
|
T | G | 1 | a0001c0001t0001g0059 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.484+20306T>G | RNF128 | ENSG00000133135.14 | transcript | ENST00000255499.3 | protein_coding | 1/6 | chrX | 106747703 | ||||||
chrX:106748029
|
A | G | 1 | a0001c0001t0001g0156 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.484+20632A>G | RNF128 | ENSG00000133135.14 | transcript | ENST00000255499.3 | protein_coding | 1/6 | chrX | 106748029 | ||||||
chrX:106748214
|
G | A | 45 | a0001c0001t0001g0003a0001c0001t0001g0018a0001c0001t0001g0027others(42): Show | 48 | HG01109.hp1 HG01243.hp1 HG01884.hp2 others(45): Show |
intron_variant | MODIFIER | c.484+20817G>A | RNF128 | ENSG00000133135.14 | transcript | ENST00000255499.3 | protein_coding | 1/6 | chrX | 106748214 | ||||||
chrX:106749904
|
C | CA | 15 | a0001c0001t0001g0003a0001c0001t0001g0018a0001c0001t0001g0027others(12): Show | 16 | HG02109.hp2 HG02486.hp1 HG02572.hp1 others(13): Show |
intron_variant | MODIFIER | c.484+22521dupA | RNF128 | ENSG00000133135.14 | transcript | ENST00000255499.3 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chrX | 106749904 | |||||
chrX:106750335
|
A | G | 14 | a0001c0001t0001g0174a0001c0001t0001g0175a0001c0001t0001g0176others(11): Show | 14 | HG01109.hp1 HG02258.hp1 HG02559.hp2 others(11): Show |
intron_variant | MODIFIER | c.485-22578A>G | RNF128 | ENSG00000133135.14 | transcript | ENST00000255499.3 | protein_coding | 1/6 | chrX | 106750335 | ||||||
chrX:106750782
|
T | A | 1 | a0001c0001t0001g0056 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.485-22131T>A | RNF128 | ENSG00000133135.14 | transcript | ENST00000255499.3 | protein_coding | 1/6 | chrX | 106750782 | ||||||
chrX:106751301
|
C | G | 1 | a0001c0001t0001g0085 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.485-21612C>G | RNF128 | ENSG00000133135.14 | transcript | ENST00000255499.3 | protein_coding | 1/6 | chrX | 106751301 | ||||||
chrX:106751317
|
A | C | 1 | a0001c0001t0001g0084 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.485-21596A>C | RNF128 | ENSG00000133135.14 | transcript | ENST00000255499.3 | protein_coding | 1/6 | chrX | 106751317 | ||||||
chrX:106751401
|
G | A | 1 | a0001c0001t0001g0060 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.485-21512G>A | RNF128 | ENSG00000133135.14 | transcript | ENST00000255499.3 | protein_coding | 1/6 | chrX | 106751401 | ||||||
chrX:106751630
|
A | G | 1 | a0001c0001t0001g0011 | 2 | HG01167.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.485-21283A>G | RNF128 | ENSG00000133135.14 | transcript | ENST00000255499.3 | protein_coding | 1/6 | chrX | 106751630 | ||||||
chrX:106751894
|
C | T | 1 | a0001c0001t0001g0109 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.485-21019C>T | RNF128 | ENSG00000133135.14 | transcript | ENST00000255499.3 | protein_coding | 1/6 | chrX | 106751894 | ||||||
chrX:106751901
|
C | T | 17 | a0001c0001t0001g0003a0001c0001t0001g0018a0001c0001t0001g0027others(14): Show | 18 | HG02109.hp1 HG02109.hp2 HG02486.hp1 others(15): Show |
intron_variant | MODIFIER | c.485-21012C>T | RNF128 | ENSG00000133135.14 | transcript | ENST00000255499.3 | protein_coding | 1/6 | chrX | 106751901 | ||||||
chrX:106751981
|
A | G | 14 | a0001c0001t0002g0002a0001c0001t0002g0004a0001c0001t0002g0017others(11): Show | 16 | HG01243.hp1 HG01884.hp2 HG02145.hp1 others(13): Show |
intron_variant | MODIFIER | c.485-20932A>G | RNF128 | ENSG00000133135.14 | transcript | ENST00000255499.3 | protein_coding | 1/6 | chrX | 106751981 | ||||||
chrX:106752143
|
A | G | 1 | a0001c0001t0001g0038 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.485-20770A>G | RNF128 | ENSG00000133135.14 | transcript | ENST00000255499.3 | protein_coding | 1/6 | chrX | 106752143 | ||||||
chrX:106752346
|
T | C | 1 | a0001c0001t0001g0160 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.485-20567T>C | RNF128 | ENSG00000133135.14 | transcript | ENST00000255499.3 | protein_coding | 1/6 | chrX | 106752346 | ||||||
chrX:106752747
|
G | A | 187 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0005others(184): Show | 206 | HG00140.hp1 HG00280.hp1 HG00438.hp1 others(203): Show |
intron_variant | MODIFIER | c.485-20166G>A | RNF128 | ENSG00000133135.14 | transcript | ENST00000255499.3 | protein_coding | 1/6 | chrX | 106752747 | ||||||
chrX:106752992
|
G | A | 7 | a0001c0001t0001g0031a0001c0001t0001g0032a0001c0001t0001g0033others(4): Show | 7 | HG02109.hp1 HG02486.hp1 HG02723.hp1 others(4): Show |
intron_variant | MODIFIER | c.485-19921G>A | RNF128 | ENSG00000133135.14 | transcript | ENST00000255499.3 | protein_coding | 1/6 | chrX | 106752992 | ||||||
chrX:106753219
|
A | T | 1 | a0001c0001t0001g0053 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.485-19694A>T | RNF128 | ENSG00000133135.14 | transcript | ENST00000255499.3 | protein_coding | 1/6 | chrX | 106753219 | ||||||
chrX:106753349
|
CTTTG | C | 9 | a0001c0001t0001g0174a0001c0001t0001g0175a0001c0001t0001g0176others(6): Show | 9 | HG01109.hp1 HG02622.hp1 HG02886.hp2 others(6): Show |
intron_variant | MODIFIER | c.485-19548_485-1954 others(8): Show |
RNF128 | ENSG00000133135.14 | transcript | ENST00000255499.3 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chrX | 106753349 | |||||
chrX:106753700
|
C | T | 32 | a0001c0001t0001g0003a0001c0001t0001g0018a0001c0001t0001g0027others(29): Show | 35 | HG01243.hp1 HG01884.hp2 HG02109.hp1 others(32): Show |
intron_variant | MODIFIER | c.485-19213C>T | RNF128 | ENSG00000133135.14 | transcript | ENST00000255499.3 | protein_coding | 1/6 | chrX | 106753700 | ||||||
chrX:106753701
|
T | G | 32 | a0001c0001t0001g0003a0001c0001t0001g0018a0001c0001t0001g0027others(29): Show | 35 | HG01243.hp1 HG01884.hp2 HG02109.hp1 others(32): Show |
intron_variant | MODIFIER | c.485-19212T>G | RNF128 | ENSG00000133135.14 | transcript | ENST00000255499.3 | protein_coding | 1/6 | chrX | 106753701 | ||||||
chrX:106754410
|
C | CT | 8 | a0001c0001t0001g0083a0001c0001t0001g0112a0001c0001t0001g0150others(5): Show | 8 | HG00738.hp1 HG01358.hp1 HG01433.hp1 others(5): Show |
intron_variant | MODIFIER | c.485-18472dupT | RNF128 | ENSG00000133135.14 | transcript | ENST00000255499.3 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chrX | 106754410 | |||||
chrX:106754410
|
C | CTT | 7 | a0001c0001t0001g0003a0001c0001t0001g0027a0001c0001t0001g0029others(4): Show | 8 | HG02109.hp2 HG02572.hp1 HG02630.hp1 others(5): Show |
intron_variant | MODIFIER | c.485-18473_485-1847 others(6): Show |
RNF128 | ENSG00000133135.14 | transcript | ENST00000255499.3 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chrX | 106754410 | |||||
chrX:106754410
|
C | CTTT | 6 | a0001c0001t0001g0028a0001c0001t0001g0031a0001c0001t0001g0032others(3): Show | 6 | HG02723.hp1 HG02886.hp1 HG02922.hp1 others(3): Show |
intron_variant | MODIFIER | c.485-18474_485-1847 others(7): Show |
RNF128 | ENSG00000133135.14 | transcript | ENST00000255499.3 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chrX | 106754410 | |||||
chrX:106754410
|
C | CTTTT | 9 | a0001c0001t0001g0038a0001c0001t0002g0017a0001c0001t0002g0019others(6): Show | 9 | HG01243.hp1 HG02109.hp1 HG02559.hp1 others(6): Show |
intron_variant | MODIFIER | c.485-18475_485-1847 others(8): Show |
RNF128 | ENSG00000133135.14 | transcript | ENST00000255499.3 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chrX | 106754410 | |||||
chrX:106754410
|
C | CTTTTT | 4 | a0001c0001t0001g0155a0001c0001t0002g0004a0001c0001t0002g0024others(1): Show | 5 | HG01884.hp2 HG02630.hp2 HG03209.hp1 others(2): Show |
intron_variant | MODIFIER | c.485-18476_485-1847 others(9): Show |
RNF128 | ENSG00000133135.14 | transcript | ENST00000255499.3 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chrX | 106754410 | |||||
chrX:106754410
|
C | CTTTTTT | 4 | a0001c0001t0002g0002a0001c0001t0002g0026a0001c0001t0002g0043others(1): Show | 5 | HG02145.hp1 HG02818.hp2 HG02895.hp1 others(2): Show |
intron_variant | MODIFIER | c.485-18477_485-1847 others(10): Show |
RNF128 | ENSG00000133135.14 | transcript | ENST00000255499.3 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chrX | 106754410 | |||||
chrX:106754410
|
C | CTTTTTTT | 1 | a0001c0001t0001g0030 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.485-18478_485-1847 others(11): Show |
RNF128 | ENSG00000133135.14 | transcript | ENST00000255499.3 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chrX | 106754410 | |||||
chrX:106754410
|
CT | C | 91 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(88): Show | 105 | HG00140.hp1 HG00280.hp1 HG00558.hp1 others(102): Show |
intron_variant | MODIFIER | c.485-18472delT | RNF128 | ENSG00000133135.14 | transcript | ENST00000255499.3 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chrX | 106754410 | |||||
chrX:106754410
|
CTT | C | 6 | a0001c0001t0001g0047a0001c0001t0001g0061a0001c0001t0001g0062others(3): Show | 6 | HG01074.hp1 HG01099.hp1 HG01169.hp2 others(3): Show |
intron_variant | MODIFIER | c.485-18473_485-1847 others(6): Show |
RNF128 | ENSG00000133135.14 | transcript | ENST00000255499.3 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chrX | 106754410 | |||||
chrX:106754410
|
CTTTTT | C | 1 | a0001c0001t0001g0018 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.485-18476_485-1847 others(9): Show |
RNF128 | ENSG00000133135.14 | transcript | ENST00000255499.3 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chrX | 106754410 | |||||
chrX:106754410
|
CTTTTTTT others(4): Show |
C | 2 | a0001c0001t0001g0037a0001c0001t0001g0042 | 2 | HG06807.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.485-18482_485-1847 others(15): Show |
RNF128 | ENSG00000133135.14 | transcript | ENST00000255499.3 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chrX | 106754410 | |||||
chrX:106754410
|
CTTTTTTT others(6): Show |
C | 1 | a0001c0001t0001g0034 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.485-18484_485-1847 others(17): Show |
RNF128 | ENSG00000133135.14 | transcript | ENST00000255499.3 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chrX | 106754410 | |||||
chrX:106754449
|
C | G | 1 | a0001c0001t0005g0052 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.485-18464C>G | RNF128 | ENSG00000133135.14 | transcript | ENST00000255499.3 | protein_coding | 1/6 | chrX | 106754449 | ||||||
chrX:106754600
|
C | T | 1 | a0001c0001t0001g0011 | 2 | HG01167.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.485-18313C>T | RNF128 | ENSG00000133135.14 | transcript | ENST00000255499.3 | protein_coding | 1/6 | chrX | 106754600 | ||||||
chrX:106754901
|
A | G | 1 | a0001c0001t0001g0033 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.485-18012A>G | RNF128 | ENSG00000133135.14 | transcript | ENST00000255499.3 | protein_coding | 1/6 | chrX | 106754901 | ||||||
chrX:106754921
|
A | G | 1 | a0001c0001t0001g0149 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.485-17992A>G | RNF128 | ENSG00000133135.14 | transcript | ENST00000255499.3 | protein_coding | 1/6 | chrX | 106754921 | ||||||
chrX:106755604
|
T | C | 2 | a0001c0001t0001g0174a0001c0001t0001g0181 | 2 | HG02976.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.485-17309T>C | RNF128 | ENSG00000133135.14 | transcript | ENST00000255499.3 | protein_coding | 1/6 | chrX | 106755604 | ||||||
chrX:106756045
|
C | T | 2 | a0001c0001t0001g0186a0001c0001t0001g0187 | 2 | HG02258.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.485-16868C>T | RNF128 | ENSG00000133135.14 | transcript | ENST00000255499.3 | protein_coding | 1/6 | chrX | 106756045 | ||||||
chrX:106756085
|
G | C | 1 | a0001c0001t0001g0074 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.485-16828G>C | RNF128 | ENSG00000133135.14 | transcript | ENST00000255499.3 | protein_coding | 1/6 | chrX | 106756085 | ||||||
chrX:106756268
|
C | T | 1 | a0001c0001t0001g0090 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.485-16645C>T | RNF128 | ENSG00000133135.14 | transcript | ENST00000255499.3 | protein_coding | 1/6 | chrX | 106756268 | ||||||
chrX:106756274
|
A | G | 1 | a0001c0001t0005g0052 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.485-16639A>G | RNF128 | ENSG00000133135.14 | transcript | ENST00000255499.3 | protein_coding | 1/6 | chrX | 106756274 | ||||||
chrX:106756424
|
A | T | 1 | a0001c0001t0001g0178 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.485-16489A>T | RNF128 | ENSG00000133135.14 | transcript | ENST00000255499.3 | protein_coding | 1/6 | chrX | 106756424 | ||||||
chrX:106756431
|
T | C | 33 | a0001c0001t0001g0003a0001c0001t0001g0018a0001c0001t0001g0027others(30): Show | 36 | HG01243.hp1 HG01884.hp2 HG02109.hp1 others(33): Show |
intron_variant | MODIFIER | c.485-16482T>C | RNF128 | ENSG00000133135.14 | transcript | ENST00000255499.3 | protein_coding | 1/6 | chrX | 106756431 | ||||||
chrX:106756551
|
C | T | 2 | a0001c0001t0001g0038a0001c0001t0001g0160 | 2 | HG01952.hp1 HG02109.hp1 |
intron_variant | MODIFIER | c.485-16362C>T | RNF128 | ENSG00000133135.14 | transcript | ENST00000255499.3 | protein_coding | 1/6 | chrX | 106756551 | ||||||
chrX:106756751
|
A | C | 1 | a0001c0001t0001g0167 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.485-16162A>C | RNF128 | ENSG00000133135.14 | transcript | ENST00000255499.3 | protein_coding | 1/6 | chrX | 106756751 | ||||||
chrX:106756825
|
C | T | 46 | a0001c0001t0001g0003a0001c0001t0001g0018a0001c0001t0001g0027others(43): Show | 49 | HG01109.hp1 HG01243.hp1 HG01884.hp2 others(46): Show |
intron_variant | MODIFIER | c.485-16088C>T | RNF128 | ENSG00000133135.14 | transcript | ENST00000255499.3 | protein_coding | 1/6 | chrX | 106756825 | ||||||
chrX:106756924
|
G | T | 2 | a0001c0001t0001g0062a0001c0001t0001g0073 | 2 | HG01168.hp2 HG01169.hp2 |
intron_variant | MODIFIER | c.485-15989G>T | RNF128 | ENSG00000133135.14 | transcript | ENST00000255499.3 | protein_coding | 1/6 | chrX | 106756924 | ||||||
chrX:106756980
|
A | G | 1 | a0001c0001t0001g0137 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.485-15933A>G | RNF128 | ENSG00000133135.14 | transcript | ENST00000255499.3 | protein_coding | 1/6 | chrX | 106756980 | ||||||
chrX:106757028
|
T | A | 2 | a0001c0001t0001g0125a0001c0001t0001g0160 | 2 | HG01952.hp1 NA20905.hp1 |
intron_variant | MODIFIER | c.485-15885T>A | RNF128 | ENSG00000133135.14 | transcript | ENST00000255499.3 | protein_coding | 1/6 | chrX | 106757028 | ||||||
chrX:106757176
|
C | T | 32 | a0001c0001t0001g0003a0001c0001t0001g0018a0001c0001t0001g0027others(29): Show | 35 | HG01243.hp1 HG01884.hp2 HG02109.hp1 others(32): Show |
intron_variant | MODIFIER | c.485-15737C>T | RNF128 | ENSG00000133135.14 | transcript | ENST00000255499.3 | protein_coding | 1/6 | chrX | 106757176 | ||||||
chrX:106757177
|
G | A | 1 | a0001c0001t0007g0075 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.485-15736G>A | RNF128 | ENSG00000133135.14 | transcript | ENST00000255499.3 | protein_coding | 1/6 | chrX | 106757177 | ||||||
chrX:106757285
|
G | A | 1 | a0001c0001t0001g0063 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.485-15628G>A | RNF128 | ENSG00000133135.14 | transcript | ENST00000255499.3 | protein_coding | 1/6 | chrX | 106757285 | ||||||
chrX:106757331
|
C | A | 1 | a0001c0001t0001g0064 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.485-15582C>A | RNF128 | ENSG00000133135.14 | transcript | ENST00000255499.3 | protein_coding | 1/6 | chrX | 106757331 | ||||||
chrX:106757347
|
A | G | 1 | a0001c0001t0001g0108 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.485-15566A>G | RNF128 | ENSG00000133135.14 | transcript | ENST00000255499.3 | protein_coding | 1/6 | chrX | 106757347 | ||||||
chrX:106757410
|
A | C | 32 | a0001c0001t0001g0003a0001c0001t0001g0018a0001c0001t0001g0027others(29): Show | 35 | HG01243.hp1 HG01884.hp2 HG02109.hp1 others(32): Show |
intron_variant | MODIFIER | c.485-15503A>C | RNF128 | ENSG00000133135.14 | transcript | ENST00000255499.3 | protein_coding | 1/6 | chrX | 106757410 | ||||||
chrX:106757477
|
C | T | 2 | a0001c0001t0001g0147a0001c0001t0001g0148 | 2 | HG03041.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.485-15436C>T | RNF128 | ENSG00000133135.14 | transcript | ENST00000255499.3 | protein_coding | 1/6 | chrX | 106757477 | ||||||
chrX:106757478
|
G | A | 9 | a0001c0001t0001g0174a0001c0001t0001g0175a0001c0001t0001g0176others(6): Show | 9 | HG01109.hp1 HG02622.hp1 HG02886.hp2 others(6): Show |
intron_variant | MODIFIER | c.485-15435G>A | RNF128 | ENSG00000133135.14 | transcript | ENST00000255499.3 | protein_coding | 1/6 | chrX | 106757478 | ||||||
chrX:106757613
|
T | C | 2 | a0001c0001t0001g0090a0001c0001t0001g0091 | 2 | HG02080.hp2 NA18955.hp1 |
intron_variant | MODIFIER | c.485-15300T>C | RNF128 | ENSG00000133135.14 | transcript | ENST00000255499.3 | protein_coding | 1/6 | chrX | 106757613 | ||||||
chrX:106757658
|
G | A | 1 | a0001c0001t0001g0139 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.485-15255G>A | RNF128 | ENSG00000133135.14 | transcript | ENST00000255499.3 | protein_coding | 1/6 | chrX | 106757658 | ||||||
chrX:106757667
|
C | T | 1 | a0001c0001t0001g0181 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.485-15246C>T | RNF128 | ENSG00000133135.14 | transcript | ENST00000255499.3 | protein_coding | 1/6 | chrX | 106757667 | ||||||
chrX:106757748
|
TA | T | 5 | a0001c0001t0001g0003a0001c0001t0001g0018a0001c0001t0001g0027others(2): Show | 6 | HG02572.hp1 HG02630.hp1 HG02809.hp2 others(3): Show |
intron_variant | MODIFIER | c.485-15157delA | RNF128 | ENSG00000133135.14 | transcript | ENST00000255499.3 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chrX | 106757748 | |||||
chrX:106758044
|
G | A | 1 | a0001c0001t0001g0050 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.485-14869G>A | RNF128 | ENSG00000133135.14 | transcript | ENST00000255499.3 | protein_coding | 1/6 | chrX | 106758044 | ||||||
chrX:106758453
|
A | G | 1 | a0001c0001t0001g0149 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.485-14460A>G | RNF128 | ENSG00000133135.14 | transcript | ENST00000255499.3 | protein_coding | 1/6 | chrX | 106758453 | ||||||
chrX:106758825
|
A | C | 1 | a0001c0001t0001g0016 | 2 | HG01069.hp1 HG01071.hp1 |
intron_variant | MODIFIER | c.485-14088A>C | RNF128 | ENSG00000133135.14 | transcript | ENST00000255499.3 | protein_coding | 1/6 | chrX | 106758825 | ||||||
chrX:106759055
|
C | G | 1 | a0001c0001t0001g0164 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.485-13858C>G | RNF128 | ENSG00000133135.14 | transcript | ENST00000255499.3 | protein_coding | 1/6 | chrX | 106759055 | ||||||
chrX:106759349
|
A | G | 1 | a0001c0001t0002g0023 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.485-13564A>G | RNF128 | ENSG00000133135.14 | transcript | ENST00000255499.3 | protein_coding | 1/6 | chrX | 106759349 | ||||||
chrX:106759531
|
C | T | 1 | a0001c0001t0001g0188 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.485-13382C>T | RNF128 | ENSG00000133135.14 | transcript | ENST00000255499.3 | protein_coding | 1/6 | chrX | 106759531 | ||||||
chrX:106761032
|
G | T | 1 | a0001c0001t0001g0146 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.485-11881G>T | RNF128 | ENSG00000133135.14 | transcript | ENST00000255499.3 | protein_coding | 1/6 | chrX | 106761032 | ||||||
chrX:106761042
|
C | T | 2 | a0001c0001t0001g0105a0001c0001t0001g0108 | 2 | HG01257.hp2 HG02293.hp2 |
intron_variant | MODIFIER | c.485-11871C>T | RNF128 | ENSG00000133135.14 | transcript | ENST00000255499.3 | protein_coding | 1/6 | chrX | 106761042 | ||||||
chrX:106761530
|
A | C | 7 | a0001c0001t0001g0031a0001c0001t0001g0032a0001c0001t0001g0033others(4): Show | 7 | HG02109.hp1 HG02486.hp1 HG02723.hp1 others(4): Show |
intron_variant | MODIFIER | c.485-11383A>C | RNF128 | ENSG00000133135.14 | transcript | ENST00000255499.3 | protein_coding | 1/6 | chrX | 106761530 | ||||||
chrX:106761599
|
TA | T | 32 | a0001c0001t0001g0003a0001c0001t0001g0018a0001c0001t0001g0027others(29): Show | 35 | HG01243.hp1 HG01884.hp2 HG02109.hp1 others(32): Show |
intron_variant | MODIFIER | c.485-11307delA | RNF128 | ENSG00000133135.14 | transcript | ENST00000255499.3 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chrX | 106761599 | |||||
chrX:106761977
|
A | G | 1 | a0001c0001t0001g0155 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.485-10936A>G | RNF128 | ENSG00000133135.14 | transcript | ENST00000255499.3 | protein_coding | 1/6 | chrX | 106761977 | ||||||
chrX:106762317
|
A | AT | 17 | a0001c0001t0001g0034a0001c0001t0001g0036a0001c0001t0002g0002others(14): Show | 19 | HG01243.hp1 HG01884.hp2 HG02145.hp1 others(16): Show |
intron_variant | MODIFIER | c.485-10581dupT | RNF128 | ENSG00000133135.14 | transcript | ENST00000255499.3 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chrX | 106762317 | |||||
chrX:106762317
|
AT | A | 8 | a0001c0001t0001g0003a0001c0001t0001g0018a0001c0001t0001g0027others(5): Show | 9 | HG01081.hp1 HG01081.hp2 HG02572.hp1 others(6): Show |
intron_variant | MODIFIER | c.485-10581delT | RNF128 | ENSG00000133135.14 | transcript | ENST00000255499.3 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chrX | 106762317 | |||||
chrX:106762401
|
T | C | 32 | a0001c0001t0001g0003a0001c0001t0001g0018a0001c0001t0001g0027others(29): Show | 35 | HG01243.hp1 HG01884.hp2 HG02109.hp1 others(32): Show |
intron_variant | MODIFIER | c.485-10512T>C | RNF128 | ENSG00000133135.14 | transcript | ENST00000255499.3 | protein_coding | 1/6 | chrX | 106762401 | ||||||
chrX:106762470
|
C | T | 2 | a0001c0001t0001g0119a0001c0001t0001g0120 | 2 | NA18965.hp1 NA19082.hp1 |
intron_variant | MODIFIER | c.485-10443C>T | RNF128 | ENSG00000133135.14 | transcript | ENST00000255499.3 | protein_coding | 1/6 | chrX | 106762470 | ||||||
chrX:106762547
|
A | G | 4 | a0001c0001t0001g0114a0001c0001t0001g0115a0001c0001t0001g0124others(1): Show | 4 | HG00735.hp2 HG01099.hp1 NA18945.hp1 others(1): Show |
intron_variant | MODIFIER | c.485-10366A>G | RNF128 | ENSG00000133135.14 | transcript | ENST00000255499.3 | protein_coding | 1/6 | chrX | 106762547 | ||||||
chrX:106762555
|
C | T | 1 | a0001c0001t0001g0155 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.485-10358C>T | RNF128 | ENSG00000133135.14 | transcript | ENST00000255499.3 | protein_coding | 1/6 | chrX | 106762555 | ||||||
chrX:106762807
|
T | A | 2 | a0001c0001t0001g0039a0001c0001t0001g0040 | 2 | HG02109.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.485-10106T>A | RNF128 | ENSG00000133135.14 | transcript | ENST00000255499.3 | protein_coding | 1/6 | chrX | 106762807 | ||||||
chrX:106763410
|
A | C | 32 | a0001c0001t0001g0003a0001c0001t0001g0018a0001c0001t0001g0027others(29): Show | 35 | HG01243.hp1 HG01884.hp2 HG02109.hp1 others(32): Show |
intron_variant | MODIFIER | c.485-9503A>C | RNF128 | ENSG00000133135.14 | transcript | ENST00000255499.3 | protein_coding | 1/6 | chrX | 106763410 | ||||||
chrX:106763422
|
G | T | 2 | a0001c0001t0001g0072a0001c0001t0001g0082 | 2 | HG01257.hp1 HG01258.hp1 |
intron_variant | MODIFIER | c.485-9491G>T | RNF128 | ENSG00000133135.14 | transcript | ENST00000255499.3 | protein_coding | 1/6 | chrX | 106763422 | ||||||
chrX:106763522
|
G | A | 17 | a0001c0001t0001g0003a0001c0001t0001g0018a0001c0001t0001g0027others(14): Show | 18 | HG02109.hp1 HG02109.hp2 HG02486.hp1 others(15): Show |
intron_variant | MODIFIER | c.485-9391G>A | RNF128 | ENSG00000133135.14 | transcript | ENST00000255499.3 | protein_coding | 1/6 | chrX | 106763522 | ||||||
chrX:106763724
|
T | C | 3 | a0001c0001t0001g0030a0001c0001t0001g0037a0001c0001t0001g0155 | 3 | HG03471.hp1 HG06807.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.485-9189T>C | RNF128 | ENSG00000133135.14 | transcript | ENST00000255499.3 | protein_coding | 1/6 | chrX | 106763724 | ||||||
chrX:106763885
|
T | C | 46 | a0001c0001t0001g0003a0001c0001t0001g0018a0001c0001t0001g0027others(43): Show | 49 | HG01109.hp1 HG01243.hp1 HG01884.hp2 others(46): Show |
intron_variant | MODIFIER | c.485-9028T>C | RNF128 | ENSG00000133135.14 | transcript | ENST00000255499.3 | protein_coding | 1/6 | chrX | 106763885 | ||||||
chrX:106763927
|
T | TTTTGG | 43 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(40): Show | 48 | HG00438.hp1 HG00558.hp1 HG00558.hp2 others(45): Show |
intron_variant | MODIFIER | c.485-8952_485-8948d others(7): Show |
RNF128 | ENSG00000133135.14 | transcript | ENST00000255499.3 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chrX | 106763927 | |||||
chrX:106763927
|
T | TTTTGGTT others(3): Show |
2 | a0001c0001t0001g0062a0001c0001t0001g0073 | 2 | HG01168.hp2 HG01169.hp2 |
intron_variant | MODIFIER | c.485-8957_485-8948d others(12): Show |
RNF128 | ENSG00000133135.14 | transcript | ENST00000255499.3 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chrX | 106763927 | |||||
chrX:106763927
|
T | TTTTGGTT others(8): Show |
15 | a0001c0001t0001g0036a0001c0001t0001g0037a0001c0001t0002g0002others(12): Show | 17 | HG01884.hp2 HG02145.hp1 HG02622.hp2 others(14): Show |
intron_variant | MODIFIER | c.485-8962_485-8948d others(17): Show |
RNF128 | ENSG00000133135.14 | transcript | ENST00000255499.3 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chrX | 106763927 | |||||
chrX:106763927
|
T | TTTTGGTT others(13): Show |
14 | a0001c0001t0001g0003a0001c0001t0001g0018a0001c0001t0001g0027others(11): Show | 15 | HG01243.hp1 HG02109.hp1 HG02109.hp2 others(12): Show |
intron_variant | MODIFIER | c.485-8967_485-8948d others(22): Show |
RNF128 | ENSG00000133135.14 | transcript | ENST00000255499.3 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chrX | 106763927 | |||||
chrX:106763927
|
T | TTTTGGTT others(18): Show |
2 | a0001c0001t0001g0034a0001c0001t0001g0155 | 2 | HG02486.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.485-8972_485-8948d others(27): Show |
RNF128 | ENSG00000133135.14 | transcript | ENST00000255499.3 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chrX | 106763927 | |||||
chrX:106763927
|
T | TTTTGGTT others(23): Show |
1 | a0001c0001t0001g0039 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.485-8977_485-8948d others(32): Show |
RNF128 | ENSG00000133135.14 | transcript | ENST00000255499.3 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chrX | 106763927 | |||||
chrX:106764063
|
C | T | 1 | a0001c0001t0001g0123 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.485-8850C>T | RNF128 | ENSG00000133135.14 | transcript | ENST00000255499.3 | protein_coding | 1/6 | chrX | 106764063 | ||||||
chrX:106764244
|
C | T | 7 | a0001c0001t0001g0031a0001c0001t0001g0032a0001c0001t0001g0033others(4): Show | 7 | HG02109.hp1 HG02486.hp1 HG02723.hp1 others(4): Show |
intron_variant | MODIFIER | c.485-8669C>T | RNF128 | ENSG00000133135.14 | transcript | ENST00000255499.3 | protein_coding | 1/6 | chrX | 106764244 | ||||||
chrX:106764303
|
C | A | 2 | a0001c0001t0001g0070a0001c0001t0001g0085 | 2 | HG00140.hp1 HG01175.hp1 |
intron_variant | MODIFIER | c.485-8610C>A | RNF128 | ENSG00000133135.14 | transcript | ENST00000255499.3 | protein_coding | 1/6 | chrX | 106764303 | ||||||
chrX:106764646
|
A | G | 32 | a0001c0001t0001g0003a0001c0001t0001g0018a0001c0001t0001g0027others(29): Show | 35 | HG01243.hp1 HG01884.hp2 HG02109.hp1 others(32): Show |
intron_variant | MODIFIER | c.485-8267A>G | RNF128 | ENSG00000133135.14 | transcript | ENST00000255499.3 | protein_coding | 1/6 | chrX | 106764646 | ||||||
chrX:106764653
|
G | A | 32 | a0001c0001t0001g0003a0001c0001t0001g0018a0001c0001t0001g0027others(29): Show | 35 | HG01243.hp1 HG01884.hp2 HG02109.hp1 others(32): Show |
intron_variant | MODIFIER | c.485-8260G>A | RNF128 | ENSG00000133135.14 | transcript | ENST00000255499.3 | protein_coding | 1/6 | chrX | 106764653 | ||||||
chrX:106764661
|
G | A | 1 | a0001c0001t0001g0100 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.485-8252G>A | RNF128 | ENSG00000133135.14 | transcript | ENST00000255499.3 | protein_coding | 1/6 | chrX | 106764661 | ||||||
chrX:106764729
|
T | A | 1 | a0001c0001t0001g0092 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.485-8184T>A | RNF128 | ENSG00000133135.14 | transcript | ENST00000255499.3 | protein_coding | 1/6 | chrX | 106764729 | ||||||
chrX:106764918
|
C | A | 1 | a0001c0001t0001g0036 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.485-7995C>A | RNF128 | ENSG00000133135.14 | transcript | ENST00000255499.3 | protein_coding | 1/6 | chrX | 106764918 | ||||||
chrX:106764992
|
A | G | 1 | a0001c0001t0001g0182 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.485-7921A>G | RNF128 | ENSG00000133135.14 | transcript | ENST00000255499.3 | protein_coding | 1/6 | chrX | 106764992 | ||||||
chrX:106765068
|
T | TC | 1 | a0001c0001t0001g0069 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.485-7841dupC | RNF128 | ENSG00000133135.14 | transcript | ENST00000255499.3 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chrX | 106765068 | |||||
chrX:106765111
|
G | A | 3 | a0001c0001t0001g0183a0001c0001t0001g0184a0001c0001t0001g0185 | 3 | HG02559.hp2 HG02897.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.485-7802G>A | RNF128 | ENSG00000133135.14 | transcript | ENST00000255499.3 | protein_coding | 1/6 | chrX | 106765111 | ||||||
chrX:106765267
|
T | C | 1 | a0001c0001t0001g0038 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.485-7646T>C | RNF128 | ENSG00000133135.14 | transcript | ENST00000255499.3 | protein_coding | 1/6 | chrX | 106765267 | ||||||
chrX:106765570
|
C | T | 1 | a0001c0001t0001g0180 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.485-7343C>T | RNF128 | ENSG00000133135.14 | transcript | ENST00000255499.3 | protein_coding | 1/6 | chrX | 106765570 | ||||||
chrX:106765631
|
G | T | 1 | a0001c0001t0001g0171 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.485-7282G>T | RNF128 | ENSG00000133135.14 | transcript | ENST00000255499.3 | protein_coding | 1/6 | chrX | 106765631 | ||||||
chrX:106765719
|
G | A | 15 | a0001c0001t0002g0002a0001c0001t0002g0004a0001c0001t0002g0017others(12): Show | 17 | HG01243.hp1 HG01884.hp2 HG02145.hp1 others(14): Show |
intron_variant | MODIFIER | c.485-7194G>A | RNF128 | ENSG00000133135.14 | transcript | ENST00000255499.3 | protein_coding | 1/6 | chrX | 106765719 | ||||||
chrX:106765750
|
C | G | 3 | a0001c0001t0001g0007a0001c0001t0001g0055a0001c0001t0001g0080 | 4 | HG00673.hp1 HG02074.hp1 HG02132.hp1 others(1): Show |
intron_variant | MODIFIER | c.485-7163C>G | RNF128 | ENSG00000133135.14 | transcript | ENST00000255499.3 | protein_coding | 1/6 | chrX | 106765750 | ||||||
chrX:106765786
|
T | A | 1 | a0001c0001t0001g0092 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.485-7127T>A | RNF128 | ENSG00000133135.14 | transcript | ENST00000255499.3 | protein_coding | 1/6 | chrX | 106765786 | ||||||
chrX:106765812
|
A | C | 15 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0011others(12): Show | 18 | HG00280.hp1 HG00735.hp1 HG00741.hp2 others(15): Show |
intron_variant | MODIFIER | c.485-7101A>C | RNF128 | ENSG00000133135.14 | transcript | ENST00000255499.3 | protein_coding | 1/6 | chrX | 106765812 | ||||||
chrX:106765827
|
C | T | 7 | a0001c0001t0001g0031a0001c0001t0001g0032a0001c0001t0001g0033others(4): Show | 7 | HG02109.hp1 HG02486.hp1 HG02723.hp1 others(4): Show |
intron_variant | MODIFIER | c.485-7086C>T | RNF128 | ENSG00000133135.14 | transcript | ENST00000255499.3 | protein_coding | 1/6 | chrX | 106765827 | ||||||
chrX:106765844
|
T | A | 2 | a0001c0001t0001g0076a0001c0001t0001g0156 | 2 | HG02738.hp1 HG04115.hp1 |
intron_variant | MODIFIER | c.485-7069T>A | RNF128 | ENSG00000133135.14 | transcript | ENST00000255499.3 | protein_coding | 1/6 | chrX | 106765844 | ||||||
chrX:106765859
|
A | ATCCC | 1 | a0001c0001t0001g0076 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.485-7053_485-7050d others(6): Show |
RNF128 | ENSG00000133135.14 | transcript | ENST00000255499.3 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chrX | 106765859 | |||||
chrX:106765937
|
C | A | 2 | a0001c0001t0001g0186a0001c0001t0001g0187 | 2 | HG02258.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.485-6976C>A | RNF128 | ENSG00000133135.14 | transcript | ENST00000255499.3 | protein_coding | 1/6 | chrX | 106765937 | ||||||
chrX:106766080
|
A | T | 1 | a0001c0001t0001g0164 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.485-6833A>T | RNF128 | ENSG00000133135.14 | transcript | ENST00000255499.3 | protein_coding | 1/6 | chrX | 106766080 | ||||||
chrX:106766165
|
G | T | 1 | a0001c0001t0001g0060 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.485-6748G>T | RNF128 | ENSG00000133135.14 | transcript | ENST00000255499.3 | protein_coding | 1/6 | chrX | 106766165 | ||||||
chrX:106766166
|
A | C | 1 | a0001c0001t0001g0060 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.485-6747A>C | RNF128 | ENSG00000133135.14 | transcript | ENST00000255499.3 | protein_coding | 1/6 | chrX | 106766166 | ||||||
chrX:106766178
|
G | A | 1 | a0001c0001t0001g0126 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.485-6735G>A | RNF128 | ENSG00000133135.14 | transcript | ENST00000255499.3 | protein_coding | 1/6 | chrX | 106766178 | ||||||
chrX:106766246
|
A | G | 1 | a0001c0001t0001g0071 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.485-6667A>G | RNF128 | ENSG00000133135.14 | transcript | ENST00000255499.3 | protein_coding | 1/6 | chrX | 106766246 | ||||||
chrX:106766248
|
A | G | 1 | a0001c0001t0001g0071 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.485-6665A>G | RNF128 | ENSG00000133135.14 | transcript | ENST00000255499.3 | protein_coding | 1/6 | chrX | 106766248 | ||||||
chrX:106766346
|
T | C | 1 | a0001c0001t0001g0127 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.485-6567T>C | RNF128 | ENSG00000133135.14 | transcript | ENST00000255499.3 | protein_coding | 1/6 | chrX | 106766346 | ||||||
chrX:106766680
|
C | T | 2 | a0001c0001t0001g0186a0001c0001t0001g0187 | 2 | HG02258.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.485-6233C>T | RNF128 | ENSG00000133135.14 | transcript | ENST00000255499.3 | protein_coding | 1/6 | chrX | 106766680 | ||||||
chrX:106766813
|
T | G | 1 | a0001c0001t0001g0188 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.485-6100T>G | RNF128 | ENSG00000133135.14 | transcript | ENST00000255499.3 | protein_coding | 1/6 | chrX | 106766813 | ||||||
chrX:106766852
|
T | G | 1 | a0001c0001t0001g0071 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.485-6061T>G | RNF128 | ENSG00000133135.14 | transcript | ENST00000255499.3 | protein_coding | 1/6 | chrX | 106766852 | ||||||
chrX:106767081
|
G | GT | 1 | a0001c0001t0001g0145 | 1 | NA19055.hp1 | intron_variant | MODIFIER | c.485-5828dupT | RNF128 | ENSG00000133135.14 | transcript | ENST00000255499.3 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chrX | 106767081 | |||||
chrX:106767328
|
G | A | 1 | a0001c0001t0001g0038 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.485-5585G>A | RNF128 | ENSG00000133135.14 | transcript | ENST00000255499.3 | protein_coding | 1/6 | chrX | 106767328 | ||||||
chrX:106767342
|
A | G | 1 | a0001c0001t0001g0167 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.485-5571A>G | RNF128 | ENSG00000133135.14 | transcript | ENST00000255499.3 | protein_coding | 1/6 | chrX | 106767342 | ||||||
chrX:106767387
|
C | T | 1 | a0001c0001t0002g0019 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.485-5526C>T | RNF128 | ENSG00000133135.14 | transcript | ENST00000255499.3 | protein_coding | 1/6 | chrX | 106767387 | ||||||
chrX:106767621
|
C | T | 1 | a0001c0001t0001g0104 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.485-5292C>T | RNF128 | ENSG00000133135.14 | transcript | ENST00000255499.3 | protein_coding | 1/6 | chrX | 106767621 | ||||||
chrX:106767812
|
TC | T | 1 | a0001c0001t0001g0127 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.485-5099delC | RNF128 | ENSG00000133135.14 | transcript | ENST00000255499.3 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chrX | 106767812 | |||||
chrX:106767911
|
G | GT | 1 | a0001c0001t0001g0127 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.485-4997dupT | RNF128 | ENSG00000133135.14 | transcript | ENST00000255499.3 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chrX | 106767911 | |||||
chrX:106767930
|
GT | G | 1 | a0001c0001t0001g0127 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.485-4981delT | RNF128 | ENSG00000133135.14 | transcript | ENST00000255499.3 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chrX | 106767930 | |||||
chrX:106768119
|
G | A | 46 | a0001c0001t0001g0003a0001c0001t0001g0018a0001c0001t0001g0027others(43): Show | 49 | HG01109.hp1 HG01243.hp1 HG01884.hp2 others(46): Show |
intron_variant | MODIFIER | c.485-4794G>A | RNF128 | ENSG00000133135.14 | transcript | ENST00000255499.3 | protein_coding | 1/6 | chrX | 106768119 | ||||||
chrX:106768133
|
AT | A | 1 | a0001c0001t0001g0127 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.485-4775delT | RNF128 | ENSG00000133135.14 | transcript | ENST00000255499.3 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chrX | 106768133 | |||||
chrX:106768187
|
T | G | 1 | a0001c0001t0003g0141 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.485-4726T>G | RNF128 | ENSG00000133135.14 | transcript | ENST00000255499.3 | protein_coding | 1/6 | chrX | 106768187 | ||||||
chrX:106768210
|
C | CT | 1 | a0001c0001t0001g0127 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.485-4703_485-4702i others(3): Show |
RNF128 | ENSG00000133135.14 | transcript | ENST00000255499.3 | protein_coding | 1/6 | chrX | 106768210 | ||||||
chrX:106768323
|
C | CG | 1 | a0001c0001t0001g0127 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.485-4588dupG | RNF128 | ENSG00000133135.14 | transcript | ENST00000255499.3 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chrX | 106768323 | |||||
chrX:106768355
|
T | G | 45 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(42): Show | 50 | HG00438.hp1 HG00558.hp1 HG00609.hp1 others(47): Show |
intron_variant | MODIFIER | c.485-4558T>G | RNF128 | ENSG00000133135.14 | transcript | ENST00000255499.3 | protein_coding | 1/6 | chrX | 106768355 | ||||||
chrX:106768412
|
A | G | 1 | a0001c0001t0001g0055 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.485-4501A>G | RNF128 | ENSG00000133135.14 | transcript | ENST00000255499.3 | protein_coding | 1/6 | chrX | 106768412 | ||||||
chrX:106768441
|
TG | T | 1 | a0001c0001t0001g0127 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.485-4469delG | RNF128 | ENSG00000133135.14 | transcript | ENST00000255499.3 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chrX | 106768441 | |||||
chrX:106768694
|
G | GT | 1 | a0001c0001t0001g0145 | 1 | NA19055.hp1 | intron_variant | MODIFIER | c.485-4213dupT | RNF128 | ENSG00000133135.14 | transcript | ENST00000255499.3 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chrX | 106768694 | |||||
chrX:106768694
|
GT | G | 1 | a0001c0001t0001g0127 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.485-4213delT | RNF128 | ENSG00000133135.14 | transcript | ENST00000255499.3 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chrX | 106768694 | |||||
chrX:106768803
|
A | G | 4 | a0001c0001t0002g0002a0001c0001t0002g0024a0001c0001t0002g0025others(1): Show | 5 | HG01884.hp2 HG02145.hp1 HG02895.hp1 others(2): Show |
intron_variant | MODIFIER | c.485-4110A>G | RNF128 | ENSG00000133135.14 | transcript | ENST00000255499.3 | protein_coding | 1/6 | chrX | 106768803 | ||||||
chrX:106768935
|
C | T | 3 | a0001c0001t0001g0118a0001c0001t0001g0119a0001c0001t0001g0120 | 3 | NA18965.hp1 NA19063.hp1 NA19082.hp1 |
intron_variant | MODIFIER | c.485-3978C>T | RNF128 | ENSG00000133135.14 | transcript | ENST00000255499.3 | protein_coding | 1/6 | chrX | 106768935 | ||||||
chrX:106768991
|
A | AG | 1 | a0001c0001t0001g0127 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.485-3921dupG | RNF128 | ENSG00000133135.14 | transcript | ENST00000255499.3 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chrX | 106768991 | |||||
chrX:106769021
|
TG | T | 1 | a0001c0001t0001g0127 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.485-3890delG | RNF128 | ENSG00000133135.14 | transcript | ENST00000255499.3 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chrX | 106769021 | |||||
chrX:106769117
|
G | A | 1 | a0001c0001t0004g0128 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.485-3796G>A | RNF128 | ENSG00000133135.14 | transcript | ENST00000255499.3 | protein_coding | 1/6 | chrX | 106769117 | ||||||
chrX:106769278
|
A | T | 15 | a0001c0001t0002g0002a0001c0001t0002g0004a0001c0001t0002g0017others(12): Show | 17 | HG01243.hp1 HG01884.hp2 HG02145.hp1 others(14): Show |
intron_variant | MODIFIER | c.485-3635A>T | RNF128 | ENSG00000133135.14 | transcript | ENST00000255499.3 | protein_coding | 1/6 | chrX | 106769278 | ||||||
chrX:106769355
|
C | CT | 1 | a0001c0001t0001g0127 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.485-3555dupT | RNF128 | ENSG00000133135.14 | transcript | ENST00000255499.3 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chrX | 106769355 | |||||
chrX:106769538
|
C | T | 2 | a0001c0001t0001g0068a0001c0001t0001g0079 | 2 | NA18988.hp1 NA18990.hp1 |
intron_variant | MODIFIER | c.485-3375C>T | RNF128 | ENSG00000133135.14 | transcript | ENST00000255499.3 | protein_coding | 1/6 | chrX | 106769538 | ||||||
chrX:106769546
|
G | GT | 135 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(132): Show | 151 | HG00140.hp1 HG00280.hp1 HG00438.hp1 others(148): Show |
intron_variant | MODIFIER | c.485-3349dupT | RNF128 | ENSG00000133135.14 | transcript | ENST00000255499.3 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chrX | 106769546 | |||||
chrX:106769546
|
G | GTT | 20 | a0001c0001t0001g0042a0001c0001t0001g0056a0001c0001t0001g0070others(17): Show | 20 | HG00735.hp1 HG00735.hp2 HG01109.hp1 others(17): Show |
intron_variant | MODIFIER | c.485-3350_485-3349d others(4): Show |
RNF128 | ENSG00000133135.14 | transcript | ENST00000255499.3 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chrX | 106769546 | |||||
chrX:106769546
|
G | GTTT | 1 | a0001c0001t0001g0177 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.485-3351_485-3349d others(5): Show |
RNF128 | ENSG00000133135.14 | transcript | ENST00000255499.3 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chrX | 106769546 | |||||
chrX:106769546
|
GT | G | 1 | a0001c0001t0001g0121 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.485-3349delT | RNF128 | ENSG00000133135.14 | transcript | ENST00000255499.3 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chrX | 106769546 | |||||
chrX:106769546
|
GTT | G | 30 | a0001c0001t0001g0003a0001c0001t0001g0018a0001c0001t0001g0027others(27): Show | 33 | HG01243.hp1 HG01884.hp2 HG02109.hp1 others(30): Show |
intron_variant | MODIFIER | c.485-3350_485-3349d others(4): Show |
RNF128 | ENSG00000133135.14 | transcript | ENST00000255499.3 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chrX | 106769546 | |||||
chrX:106769598
|
C | A | 1 | a0001c0001t0001g0129 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.485-3315C>A | RNF128 | ENSG00000133135.14 | transcript | ENST00000255499.3 | protein_coding | 1/6 | chrX | 106769598 | ||||||
chrX:106769705
|
C | T | 46 | a0001c0001t0001g0003a0001c0001t0001g0018a0001c0001t0001g0027others(43): Show | 49 | HG01109.hp1 HG01243.hp1 HG01884.hp2 others(46): Show |
intron_variant | MODIFIER | c.485-3208C>T | RNF128 | ENSG00000133135.14 | transcript | ENST00000255499.3 | protein_coding | 1/6 | chrX | 106769705 | ||||||
chrX:106769800
|
A | G | 1 | a0001c0001t0001g0054 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.485-3113A>G | RNF128 | ENSG00000133135.14 | transcript | ENST00000255499.3 | protein_coding | 1/6 | chrX | 106769800 | ||||||
chrX:106769884
|
G | T | 4 | a0001c0001t0001g0083a0001c0001t0001g0152a0001c0001t0001g0153others(1): Show | 4 | HG01884.hp1 HG01981.hp2 HG03710.hp1 others(1): Show |
intron_variant | MODIFIER | c.485-3029G>T | RNF128 | ENSG00000133135.14 | transcript | ENST00000255499.3 | protein_coding | 1/6 | chrX | 106769884 | ||||||
chrX:106770093
|
A | T | 3 | a0001c0001t0001g0045a0001c0001t0001g0049a0001c0001t0001g0050 | 3 | HG03540.hp1 NA18906.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.485-2820A>T | RNF128 | ENSG00000133135.14 | transcript | ENST00000255499.3 | protein_coding | 1/6 | chrX | 106770093 | ||||||
chrX:106770105
|
G | A | 2 | a0001c0001t0002g0002a0001c0001t0002g0024 | 3 | HG01884.hp2 HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.485-2808G>A | RNF128 | ENSG00000133135.14 | transcript | ENST00000255499.3 | protein_coding | 1/6 | chrX | 106770105 | ||||||
chrX:106770150
|
C | T | 1 | a0001c0001t0001g0056 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.485-2763C>T | RNF128 | ENSG00000133135.14 | transcript | ENST00000255499.3 | protein_coding | 1/6 | chrX | 106770150 | ||||||
chrX:106770344
|
C | T | 1 | a0001c0001t0001g0107 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.485-2569C>T | RNF128 | ENSG00000133135.14 | transcript | ENST00000255499.3 | protein_coding | 1/6 | chrX | 106770344 | ||||||
chrX:106770623
|
A | G | 2 | a0001c0001t0001g0032a0001c0001t0001g0033 | 2 | HG02723.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.485-2290A>G | RNF128 | ENSG00000133135.14 | transcript | ENST00000255499.3 | protein_coding | 1/6 | chrX | 106770623 | ||||||
chrX:106771417
|
C | T | 1 | a0001c0001t0001g0169 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.485-1496C>T | RNF128 | ENSG00000133135.14 | transcript | ENST00000255499.3 | protein_coding | 1/6 | chrX | 106771417 | ||||||
chrX:106771455
|
G | A | 1 | a0001c0001t0001g0054 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.485-1458G>A | RNF128 | ENSG00000133135.14 | transcript | ENST00000255499.3 | protein_coding | 1/6 | chrX | 106771455 | ||||||
chrX:106771557
|
C | T | 15 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0011others(12): Show | 18 | HG00280.hp1 HG00735.hp1 HG00741.hp2 others(15): Show |
intron_variant | MODIFIER | c.485-1356C>T | RNF128 | ENSG00000133135.14 | transcript | ENST00000255499.3 | protein_coding | 1/6 | chrX | 106771557 | ||||||
chrX:106771843
|
A | T | 1 | a0001c0001t0001g0054 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.485-1070A>T | RNF128 | ENSG00000133135.14 | transcript | ENST00000255499.3 | protein_coding | 1/6 | chrX | 106771843 | ||||||
chrX:106772032
|
A | T | 1 | a0001c0001t0001g0030 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.485-881A>T | RNF128 | ENSG00000133135.14 | transcript | ENST00000255499.3 | protein_coding | 1/6 | chrX | 106772032 | ||||||
chrX:106772108
|
A | T | 42 | a0001c0001t0001g0001a0001c0001t0001g0013a0001c0001t0001g0014others(39): Show | 49 | HG00438.hp2 HG00558.hp2 HG00735.hp2 others(46): Show |
intron_variant | MODIFIER | c.485-805A>T | RNF128 | ENSG00000133135.14 | transcript | ENST00000255499.3 | protein_coding | 1/6 | chrX | 106772108 | ||||||
chrX:106772145
|
AT | A | 9 | a0001c0001t0001g0174a0001c0001t0001g0175a0001c0001t0001g0176others(6): Show | 9 | HG01109.hp1 HG02622.hp1 HG02886.hp2 others(6): Show |
intron_variant | MODIFIER | c.485-761delT | RNF128 | ENSG00000133135.14 | transcript | ENST00000255499.3 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chrX | 106772145 | |||||
chrX:106772164
|
A | G | 17 | a0001c0001t0001g0003a0001c0001t0001g0018a0001c0001t0001g0027others(14): Show | 18 | HG02109.hp1 HG02109.hp2 HG02486.hp1 others(15): Show |
intron_variant | MODIFIER | c.485-749A>G | RNF128 | ENSG00000133135.14 | transcript | ENST00000255499.3 | protein_coding | 1/6 | chrX | 106772164 | ||||||
chrX:106772504
|
G | T | 1 | a0001c0001t0001g0164 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.485-409G>T | RNF128 | ENSG00000133135.14 | transcript | ENST00000255499.3 | protein_coding | 1/6 | chrX | 106772504 | ||||||
chrX:106772568
|
T | TG | 1 | a0001c0001t0001g0083 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.485-340dupG | RNF128 | ENSG00000133135.14 | transcript | ENST00000255499.3 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chrX | 106772568 | |||||
chrX:106772648
|
A | G | 1 | a0001c0001t0001g0127 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.485-265A>G | RNF128 | ENSG00000133135.14 | transcript | ENST00000255499.3 | protein_coding | 1/6 | chrX | 106772648 | ||||||
chrX:106772750
|
A | G | 32 | a0001c0001t0001g0003a0001c0001t0001g0018a0001c0001t0001g0027others(29): Show | 35 | HG01243.hp1 HG01884.hp2 HG02109.hp1 others(32): Show |
intron_variant | MODIFIER | c.485-163A>G | RNF128 | ENSG00000133135.14 | transcript | ENST00000255499.3 | protein_coding | 1/6 | chrX | 106772750 | ||||||
chrX:106772866
|
C | T | 1 | a0001c0001t0001g0155 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.485-47C>T | RNF128 | ENSG00000133135.14 | transcript | ENST00000255499.3 | protein_coding | 1/6 | chrX | 106772866 | ||||||
chrX:106773202
|
T | C | 1 | a0001c0001t0001g0030 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.732+42T>C | RNF128 | ENSG00000133135.14 | transcript | ENST00000255499.3 | protein_coding | 2/6 | chrX | 106773202 | ||||||
chrX:106773321
|
G | T | 60 | a0001c0001t0001g0001a0001c0001t0001g0013a0001c0001t0001g0014others(57): Show | 67 | HG00438.hp2 HG00558.hp2 HG00735.hp2 others(64): Show |
intron_variant | MODIFIER | c.732+161G>T | RNF128 | ENSG00000133135.14 | transcript | ENST00000255499.3 | protein_coding | 2/6 | chrX | 106773321 | ||||||
chrX:106773474
|
A | G | 32 | a0001c0001t0001g0003a0001c0001t0001g0018a0001c0001t0001g0027others(29): Show | 35 | HG01243.hp1 HG01884.hp2 HG02109.hp1 others(32): Show |
intron_variant | MODIFIER | c.732+314A>G | RNF128 | ENSG00000133135.14 | transcript | ENST00000255499.3 | protein_coding | 2/6 | chrX | 106773474 | ||||||
chrX:106774257
|
A | G | 1 | a0001c0001t0001g0078 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.732+1097A>G | RNF128 | ENSG00000133135.14 | transcript | ENST00000255499.3 | protein_coding | 2/6 | chrX | 106774257 | ||||||
chrX:106774291
|
G | A | 1 | a0001c0001t0001g0034 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.732+1131G>A | RNF128 | ENSG00000133135.14 | transcript | ENST00000255499.3 | protein_coding | 2/6 | chrX | 106774291 | ||||||
chrX:106774344
|
T | A | 1 | a0001c0001t0001g0057 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.732+1184T>A | RNF128 | ENSG00000133135.14 | transcript | ENST00000255499.3 | protein_coding | 2/6 | chrX | 106774344 | ||||||
chrX:106774391
|
T | G | 1 | a0001c0001t0001g0057 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.732+1231T>G | RNF128 | ENSG00000133135.14 | transcript | ENST00000255499.3 | protein_coding | 2/6 | chrX | 106774391 | ||||||
chrX:106774413
|
C | T | 3 | a0001c0001t0001g0006a0001c0001t0001g0064a0001c0001t0001g0078 | 4 | HG00609.hp1 HG02155.hp2 HG04199.hp1 others(1): Show |
intron_variant | MODIFIER | c.732+1253C>T | RNF128 | ENSG00000133135.14 | transcript | ENST00000255499.3 | protein_coding | 2/6 | chrX | 106774413 | ||||||
chrX:106774852
|
G | A | 1 | a0001c0001t0002g0044 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.732+1692G>A | RNF128 | ENSG00000133135.14 | transcript | ENST00000255499.3 | protein_coding | 2/6 | chrX | 106774852 | ||||||
chrX:106775190
|
T | C | 2 | a0001c0001t0001g0186a0001c0001t0001g0187 | 2 | HG02258.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.732+2030T>C | RNF128 | ENSG00000133135.14 | transcript | ENST00000255499.3 | protein_coding | 2/6 | chrX | 106775190 | ||||||
chrX:106775512
|
G | A | 2 | a0001c0001t0002g0004a0001c0001t0002g0043 | 3 | HG02630.hp2 HG03209.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.732+2352G>A | RNF128 | ENSG00000133135.14 | transcript | ENST00000255499.3 | protein_coding | 2/6 | chrX | 106775512 | ||||||
chrX:106776107
|
CG | C | 1 | a0001c0001t0001g0145 | 1 | NA19055.hp1 | intron_variant | MODIFIER | c.732+2950delG | RNF128 | ENSG00000133135.14 | transcript | ENST00000255499.3 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chrX | 106776107 | |||||
chrX:106776557
|
A | C | 3 | a0001c0001t0001g0030a0001c0001t0001g0037a0001c0001t0001g0155 | 3 | HG03471.hp1 HG06807.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.732+3397A>C | RNF128 | ENSG00000133135.14 | transcript | ENST00000255499.3 | protein_coding | 2/6 | chrX | 106776557 | ||||||
chrX:106776765
|
T | C | 1 | a0001c0001t0001g0122 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.732+3605T>C | RNF128 | ENSG00000133135.14 | transcript | ENST00000255499.3 | protein_coding | 2/6 | chrX | 106776765 | ||||||
chrX:106777057
|
G | A | 1 | a0001c0001t0001g0123 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.732+3897G>A | RNF128 | ENSG00000133135.14 | transcript | ENST00000255499.3 | protein_coding | 2/6 | chrX | 106777057 | ||||||
chrX:106777184
|
C | T | 32 | a0001c0001t0001g0003a0001c0001t0001g0018a0001c0001t0001g0027others(29): Show | 35 | HG01243.hp1 HG01884.hp2 HG02109.hp1 others(32): Show |
intron_variant | MODIFIER | c.732+4024C>T | RNF128 | ENSG00000133135.14 | transcript | ENST00000255499.3 | protein_coding | 2/6 | chrX | 106777184 | ||||||
chrX:106777197
|
A | G | 1 | a0001c0001t0001g0089 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.732+4037A>G | RNF128 | ENSG00000133135.14 | transcript | ENST00000255499.3 | protein_coding | 2/6 | chrX | 106777197 | ||||||
chrX:106777557
|
C | G | 3 | a0001c0001t0001g0030a0001c0001t0001g0037a0001c0001t0001g0155 | 3 | HG03471.hp1 HG06807.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.732+4397C>G | RNF128 | ENSG00000133135.14 | transcript | ENST00000255499.3 | protein_coding | 2/6 | chrX | 106777557 | ||||||
chrX:106777583
|
C | T | 1 | a0001c0001t0001g0148 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.732+4423C>T | RNF128 | ENSG00000133135.14 | transcript | ENST00000255499.3 | protein_coding | 2/6 | chrX | 106777583 | ||||||
chrX:106777731
|
A | T | 3 | a0001c0001t0001g0183a0001c0001t0001g0184a0001c0001t0001g0185 | 3 | HG02559.hp2 HG02897.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.732+4571A>T | RNF128 | ENSG00000133135.14 | transcript | ENST00000255499.3 | protein_coding | 2/6 | chrX | 106777731 | ||||||
chrX:106778264
|
T | C | 1 | a0001c0001t0001g0088 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.732+5104T>C | RNF128 | ENSG00000133135.14 | transcript | ENST00000255499.3 | protein_coding | 2/6 | chrX | 106778264 | ||||||
chrX:106778271
|
A | G | 1 | a0001c0001t0001g0100 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.732+5111A>G | RNF128 | ENSG00000133135.14 | transcript | ENST00000255499.3 | protein_coding | 2/6 | chrX | 106778271 | ||||||
chrX:106779032
|
T | A | 1 | a0001c0001t0001g0045 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.732+5872T>A | RNF128 | ENSG00000133135.14 | transcript | ENST00000255499.3 | protein_coding | 2/6 | chrX | 106779032 | ||||||
chrX:106779189
|
A | G | 1 | a0001c0001t0001g0097 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.733-5876A>G | RNF128 | ENSG00000133135.14 | transcript | ENST00000255499.3 | protein_coding | 2/6 | chrX | 106779189 | ||||||
chrX:106779348
|
C | CGT | 37 | a0001c0001t0001g0027a0001c0001t0001g0037a0001c0001t0001g0070others(34): Show | 39 | HG00140.hp1 HG01109.hp1 HG01175.hp1 others(36): Show |
intron_variant | MODIFIER | c.733-5676_733-5675d others(4): Show |
RNF128 | ENSG00000133135.14 | transcript | ENST00000255499.3 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chrX | 106779348 | |||||
chrX:106779348
|
C | CGTGT | 26 | a0001c0001t0001g0010a0001c0001t0001g0016a0001c0001t0001g0018others(23): Show | 28 | HG00280.hp1 HG00738.hp1 HG01069.hp1 others(25): Show |
intron_variant | MODIFIER | c.733-5678_733-5675d others(6): Show |
RNF128 | ENSG00000133135.14 | transcript | ENST00000255499.3 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chrX | 106779348 | |||||
chrX:106779348
|
C | CGTGTGT | 11 | a0001c0001t0001g0003a0001c0001t0001g0028a0001c0001t0001g0029others(8): Show | 12 | HG01981.hp1 HG02630.hp1 HG02647.hp1 others(9): Show |
intron_variant | MODIFIER | c.733-5680_733-5675d others(8): Show |
RNF128 | ENSG00000133135.14 | transcript | ENST00000255499.3 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chrX | 106779348 | |||||
chrX:106779348
|
C | CGTGTGTG others(1): Show |
4 | a0001c0001t0001g0034a0001c0001t0001g0035a0001c0001t0001g0036others(1): Show | 4 | HG02109.hp1 HG02486.hp1 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.733-5682_733-5675d others(10): Show |
RNF128 | ENSG00000133135.14 | transcript | ENST00000255499.3 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chrX | 106779348 | |||||
chrX:106779348
|
C | CGTGTGTG others(3): Show |
2 | a0001c0001t0001g0031a0001c0001t0001g0033 | 2 | HG02723.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.733-5684_733-5675d others(12): Show |
RNF128 | ENSG00000133135.14 | transcript | ENST00000255499.3 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chrX | 106779348 | |||||
chrX:106779348
|
CGT | C | 7 | a0001c0001t0001g0014a0001c0001t0001g0053a0001c0001t0001g0068others(4): Show | 8 | HG01175.hp2 HG01516.hp2 HG01934.hp1 others(5): Show |
intron_variant | MODIFIER | c.733-5676_733-5675d others(4): Show |
RNF128 | ENSG00000133135.14 | transcript | ENST00000255499.3 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chrX | 106779348 | |||||
chrX:106779348
|
CGTGT | C | 3 | a0001c0001t0001g0006a0001c0001t0001g0064a0001c0001t0001g0078 | 4 | HG00609.hp1 HG02155.hp2 HG04199.hp1 others(1): Show |
intron_variant | MODIFIER | c.733-5678_733-5675d others(6): Show |
RNF128 | ENSG00000133135.14 | transcript | ENST00000255499.3 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chrX | 106779348 | |||||
chrX:106779348
|
CGTGTGTG others(7): Show |
C | 1 | a0001c0001t0002g0017 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.733-5688_733-5675d others(16): Show |
RNF128 | ENSG00000133135.14 | transcript | ENST00000255499.3 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chrX | 106779348 | |||||
chrX:106779607
|
G | GA | 7 | a0001c0001t0001g0031a0001c0001t0001g0032a0001c0001t0001g0033others(4): Show | 7 | HG02109.hp1 HG02486.hp1 HG02723.hp1 others(4): Show |
intron_variant | MODIFIER | c.733-5451dupA | RNF128 | ENSG00000133135.14 | transcript | ENST00000255499.3 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chrX | 106779607 | |||||
chrX:106779663
|
C | T | 1 | a0001c0001t0001g0135 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.733-5402C>T | RNF128 | ENSG00000133135.14 | transcript | ENST00000255499.3 | protein_coding | 2/6 | chrX | 106779663 | ||||||
chrX:106779748
|
C | T | 1 | a0001c0001t0001g0090 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.733-5317C>T | RNF128 | ENSG00000133135.14 | transcript | ENST00000255499.3 | protein_coding | 2/6 | chrX | 106779748 | ||||||
chrX:106779897
|
A | G | 7 | a0001c0001t0001g0031a0001c0001t0001g0032a0001c0001t0001g0033others(4): Show | 7 | HG02109.hp1 HG02486.hp1 HG02723.hp1 others(4): Show |
intron_variant | MODIFIER | c.733-5168A>G | RNF128 | ENSG00000133135.14 | transcript | ENST00000255499.3 | protein_coding | 2/6 | chrX | 106779897 | ||||||
chrX:106780370
|
G | GA | 15 | a0001c0001t0002g0002a0001c0001t0002g0004a0001c0001t0002g0017others(12): Show | 17 | HG01243.hp1 HG01884.hp2 HG02145.hp1 others(14): Show |
intron_variant | MODIFIER | c.733-4687dupA | RNF128 | ENSG00000133135.14 | transcript | ENST00000255499.3 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chrX | 106780370 | |||||
chrX:106781231
|
A | T | 2 | a0001c0001t0001g0093a0001c0001t0001g0094 | 2 | NA18959.hp1 NA19000.hp1 |
intron_variant | MODIFIER | c.733-3834A>T | RNF128 | ENSG00000133135.14 | transcript | ENST00000255499.3 | protein_coding | 2/6 | chrX | 106781231 | ||||||
chrX:106781336
|
G | GT | 1 | a0001c0001t0001g0040 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.733-3723dupT | RNF128 | ENSG00000133135.14 | transcript | ENST00000255499.3 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chrX | 106781336 | |||||
chrX:106781362
|
A | G | 1 | a0001c0001t0002g0041 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.733-3703A>G | RNF128 | ENSG00000133135.14 | transcript | ENST00000255499.3 | protein_coding | 2/6 | chrX | 106781362 | ||||||
chrX:106781507
|
C | T | 3 | a0001c0001t0001g0030a0001c0001t0001g0037a0001c0001t0001g0155 | 3 | HG03471.hp1 HG06807.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.733-3558C>T | RNF128 | ENSG00000133135.14 | transcript | ENST00000255499.3 | protein_coding | 2/6 | chrX | 106781507 | ||||||
chrX:106781529
|
A | G | 17 | a0001c0001t0001g0003a0001c0001t0001g0018a0001c0001t0001g0027others(14): Show | 18 | HG02109.hp1 HG02109.hp2 HG02486.hp1 others(15): Show |
intron_variant | MODIFIER | c.733-3536A>G | RNF128 | ENSG00000133135.14 | transcript | ENST00000255499.3 | protein_coding | 2/6 | chrX | 106781529 | ||||||
chrX:106781912
|
C | A | 2 | a0001c0001t0001g0010a0001c0001t0001g0099 | 3 | HG00280.hp1 HG04204.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.733-3153C>A | RNF128 | ENSG00000133135.14 | transcript | ENST00000255499.3 | protein_coding | 2/6 | chrX | 106781912 | ||||||
chrX:106782225
|
C | CT | 1 | a0001c0001t0001g0163 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.733-2837dupT | RNF128 | ENSG00000133135.14 | transcript | ENST00000255499.3 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chrX | 106782225 | |||||
chrX:106782487
|
A | G | 5 | a0001c0001t0001g0003a0001c0001t0001g0018a0001c0001t0001g0027others(2): Show | 6 | HG02572.hp1 HG02630.hp1 HG02809.hp2 others(3): Show |
intron_variant | MODIFIER | c.733-2578A>G | RNF128 | ENSG00000133135.14 | transcript | ENST00000255499.3 | protein_coding | 2/6 | chrX | 106782487 | ||||||
chrX:106782683
|
G | A | 2 | a0001c0001t0001g0186a0001c0001t0001g0187 | 2 | HG02258.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.733-2382G>A | RNF128 | ENSG00000133135.14 | transcript | ENST00000255499.3 | protein_coding | 2/6 | chrX | 106782683 | ||||||
chrX:106782688
|
T | TA | 1 | a0001c0001t0001g0028 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.733-2371dupA | RNF128 | ENSG00000133135.14 | transcript | ENST00000255499.3 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chrX | 106782688 | |||||
chrX:106782848
|
TC | T | 1 | a0001c0001t0001g0013 | 2 | NA18982.hp1 NA19007.hp1 |
intron_variant | MODIFIER | c.733-2215delC | RNF128 | ENSG00000133135.14 | transcript | ENST00000255499.3 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chrX | 106782848 | |||||
chrX:106782897
|
G | A | 1 | a0001c0001t0001g0122 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.733-2168G>A | RNF128 | ENSG00000133135.14 | transcript | ENST00000255499.3 | protein_coding | 2/6 | chrX | 106782897 | ||||||
chrX:106782996
|
TC | T | 1 | a0001c0001t0001g0093 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.733-2066delC | RNF128 | ENSG00000133135.14 | transcript | ENST00000255499.3 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chrX | 106782996 | |||||
chrX:106783008
|
AT | A | 1 | a0001c0001t0001g0093 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.733-2050delT | RNF128 | ENSG00000133135.14 | transcript | ENST00000255499.3 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chrX | 106783008 | |||||
chrX:106783022
|
C | T | 1 | a0001c0001t0001g0049 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.733-2043C>T | RNF128 | ENSG00000133135.14 | transcript | ENST00000255499.3 | protein_coding | 2/6 | chrX | 106783022 | ||||||
chrX:106783215
|
C | T | 3 | a0001c0001t0001g0118a0001c0001t0001g0119a0001c0001t0001g0120 | 3 | NA18965.hp1 NA19063.hp1 NA19082.hp1 |
intron_variant | MODIFIER | c.733-1850C>T | RNF128 | ENSG00000133135.14 | transcript | ENST00000255499.3 | protein_coding | 2/6 | chrX | 106783215 | ||||||
chrX:106783271
|
C | A | 1 | a0001c0001t0001g0167 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.733-1794C>A | RNF128 | ENSG00000133135.14 | transcript | ENST00000255499.3 | protein_coding | 2/6 | chrX | 106783271 | ||||||
chrX:106783448
|
ATACT | A | 1 | a0001c0001t0001g0123 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.733-1613_733-1610d others(6): Show |
RNF128 | ENSG00000133135.14 | transcript | ENST00000255499.3 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chrX | 106783448 | |||||
chrX:106783561
|
C | T | 1 | a0001c0001t0001g0146 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.733-1504C>T | RNF128 | ENSG00000133135.14 | transcript | ENST00000255499.3 | protein_coding | 2/6 | chrX | 106783561 | ||||||
chrX:106783809
|
G | T | 1 | a0001c0001t0001g0040 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.733-1256G>T | RNF128 | ENSG00000133135.14 | transcript | ENST00000255499.3 | protein_coding | 2/6 | chrX | 106783809 | ||||||
chrX:106783857
|
C | T | 32 | a0001c0001t0001g0003a0001c0001t0001g0018a0001c0001t0001g0027others(29): Show | 35 | HG01243.hp1 HG01884.hp2 HG02109.hp1 others(32): Show |
intron_variant | MODIFIER | c.733-1208C>T | RNF128 | ENSG00000133135.14 | transcript | ENST00000255499.3 | protein_coding | 2/6 | chrX | 106783857 | ||||||
chrX:106783858
|
G | A | 43 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(40): Show | 48 | HG00438.hp1 HG00558.hp1 HG00609.hp1 others(45): Show |
intron_variant | MODIFIER | c.733-1207G>A | RNF128 | ENSG00000133135.14 | transcript | ENST00000255499.3 | protein_coding | 2/6 | chrX | 106783858 | ||||||
chrX:106784041
|
A | G | 1 | a0001c0001t0001g0095 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.733-1024A>G | RNF128 | ENSG00000133135.14 | transcript | ENST00000255499.3 | protein_coding | 2/6 | chrX | 106784041 | ||||||
chrX:106784499
|
C | T | 1 | a0001c0001t0001g0030 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.733-566C>T | RNF128 | ENSG00000133135.14 | transcript | ENST00000255499.3 | protein_coding | 2/6 | chrX | 106784499 | ||||||
chrX:106784539
|
T | C | 3 | a0001c0001t0001g0183a0001c0001t0001g0184a0001c0001t0001g0185 | 3 | HG02559.hp2 HG02897.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.733-526T>C | RNF128 | ENSG00000133135.14 | transcript | ENST00000255499.3 | protein_coding | 2/6 | chrX | 106784539 | ||||||
chrX:106784581
|
A | G | 1 | a0001c0001t0002g0026 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.733-484A>G | RNF128 | ENSG00000133135.14 | transcript | ENST00000255499.3 | protein_coding | 2/6 | chrX | 106784581 | ||||||
chrX:106785032
|
T | C | 1 | a0001c0001t0002g0017 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.733-33T>C | RNF128 | ENSG00000133135.14 | transcript | ENST00000255499.3 | protein_coding | 2/6 | chrX | 106785032 | ||||||
chrX:106785049
|
G | GT | 2 | a0001c0001t0001g0031a0001c0001t0002g0019 | 2 | HG01243.hp1 HG03486.hp1 |
splice_region_variant&intron_variant | LOW | c.733-5dupT | RNF128 | ENSG00000133135.14 | transcript | ENST00000255499.3 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chrX | 106785049 | |||||
chrX:106785182
|
C | T | 15 | a0001c0001t0002g0002a0001c0001t0002g0004a0001c0001t0002g0017others(12): Show | 17 | HG01243.hp1 HG01884.hp2 HG02145.hp1 others(14): Show |
intron_variant | MODIFIER | c.804+46C>T | RNF128 | ENSG00000133135.14 | transcript | ENST00000255499.3 | protein_coding | 3/6 | chrX | 106785182 | ||||||
chrX:106785278
|
G | T | 2 | a0001c0001t0001g0106a0001c0001t0001g0134 | 2 | HG00741.hp1 HG01192.hp1 |
intron_variant | MODIFIER | c.804+142G>T | RNF128 | ENSG00000133135.14 | transcript | ENST00000255499.3 | protein_coding | 3/6 | chrX | 106785278 | ||||||
chrX:106785279
|
C | T | 2 | a0001c0001t0001g0106a0001c0001t0001g0134 | 2 | HG00741.hp1 HG01192.hp1 |
intron_variant | MODIFIER | c.804+143C>T | RNF128 | ENSG00000133135.14 | transcript | ENST00000255499.3 | protein_coding | 3/6 | chrX | 106785279 | ||||||
chrX:106785651
|
G | A | 1 | a0001c0001t0001g0080 | 1 | NA19004.hp1 | intron_variant | MODIFIER | c.804+515G>A | RNF128 | ENSG00000133135.14 | transcript | ENST00000255499.3 | protein_coding | 3/6 | chrX | 106785651 | ||||||
chrX:106786204
|
G | A | 1 | a0001c0001t0001g0155 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.804+1068G>A | RNF128 | ENSG00000133135.14 | transcript | ENST00000255499.3 | protein_coding | 3/6 | chrX | 106786204 | ||||||
chrX:106786221
|
G | GATTTATA others(29): Show |
1 | a0001c0001t0001g0067 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.804+1087_804+1122d others(38): Show |
RNF128 | ENSG00000133135.14 | transcript | ENST00000255499.3 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chrX | 106786221 | |||||
chrX:106786425
|
TC | T | 1 | a0001c0001t0001g0067 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.804+1291delC | RNF128 | ENSG00000133135.14 | transcript | ENST00000255499.3 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chrX | 106786425 | |||||
chrX:106786536
|
A | C | 1 | a0001c0001t0001g0036 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.805-1382A>C | RNF128 | ENSG00000133135.14 | transcript | ENST00000255499.3 | protein_coding | 3/6 | chrX | 106786536 | ||||||
chrX:106786592
|
A | C | 15 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0011others(12): Show | 18 | HG00280.hp1 HG00735.hp1 HG00741.hp2 others(15): Show |
intron_variant | MODIFIER | c.805-1326A>C | RNF128 | ENSG00000133135.14 | transcript | ENST00000255499.3 | protein_coding | 3/6 | chrX | 106786592 | ||||||
chrX:106786709
|
G | GT | 1 | a0001c0001t0001g0031 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.805-1207dupT | RNF128 | ENSG00000133135.14 | transcript | ENST00000255499.3 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chrX | 106786709 | |||||
chrX:106787155
|
G | GC | 1 | a0001c0001t0001g0067 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.805-762dupC | RNF128 | ENSG00000133135.14 | transcript | ENST00000255499.3 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chrX | 106787155 | |||||
chrX:106787221
|
A | C | 1 | a0001c0001t0001g0092 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.805-697A>C | RNF128 | ENSG00000133135.14 | transcript | ENST00000255499.3 | protein_coding | 3/6 | chrX | 106787221 | ||||||
chrX:106787384
|
CG | C | 1 | a0001c0001t0001g0067 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.805-530delG | RNF128 | ENSG00000133135.14 | transcript | ENST00000255499.3 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chrX | 106787384 | |||||
chrX:106788284
|
A | AT | 1 | a0001c0001t0001g0067 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.887+285dupT | RNF128 | ENSG00000133135.14 | transcript | ENST00000255499.3 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chrX | 106788284 | |||||
chrX:106788286
|
A | AT | 1 | a0001c0001t0001g0031 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.887+288dupT | RNF128 | ENSG00000133135.14 | transcript | ENST00000255499.3 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chrX | 106788286 | |||||
chrX:106788328
|
T | C | 1 | a0001c0001t0001g0171 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.887+328T>C | RNF128 | ENSG00000133135.14 | transcript | ENST00000255499.3 | protein_coding | 4/6 | chrX | 106788328 | ||||||
chrX:106788332
|
T | C | 1 | a0001c0001t0001g0178 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.887+332T>C | RNF128 | ENSG00000133135.14 | transcript | ENST00000255499.3 | protein_coding | 4/6 | chrX | 106788332 | ||||||
chrX:106788332
|
T | TACTATAT others(18): Show |
1 | a0001c0001t0001g0186 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.887+333_887+357dup others(25): Show |
RNF128 | ENSG00000133135.14 | transcript | ENST00000255499.3 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chrX | 106788332 | |||||
chrX:106788334
|
C | A | 1 | a0001c0001t0001g0081 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.887+334C>A | RNF128 | ENSG00000133135.14 | transcript | ENST00000255499.3 | protein_coding | 4/6 | chrX | 106788334 | ||||||
chrX:106788357
|
C | T | 15 | a0001c0001t0002g0002a0001c0001t0002g0004a0001c0001t0002g0017others(12): Show | 17 | HG01243.hp1 HG01884.hp2 HG02145.hp1 others(14): Show |
intron_variant | MODIFIER | c.887+357C>T | RNF128 | ENSG00000133135.14 | transcript | ENST00000255499.3 | protein_coding | 4/6 | chrX | 106788357 | ||||||
chrX:106788366
|
A | T | 1 | a0001c0001t0001g0184 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.887+366A>T | RNF128 | ENSG00000133135.14 | transcript | ENST00000255499.3 | protein_coding | 4/6 | chrX | 106788366 | ||||||
chrX:106788372
|
AT | A | 1 | a0001c0001t0001g0031 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.887+374delT | RNF128 | ENSG00000133135.14 | transcript | ENST00000255499.3 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chrX | 106788372 | |||||
chrX:106788373
|
TTA | T | 1 | a0001c0001t0001g0133 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.887+379_887+380del others(2): Show |
RNF128 | ENSG00000133135.14 | transcript | ENST00000255499.3 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chrX | 106788373 | |||||
chrX:106788373
|
TTATATAT others(9): Show |
T | 4 | a0001c0001t0002g0002a0001c0001t0002g0024a0001c0001t0002g0025others(1): Show | 5 | HG01884.hp2 HG02145.hp1 HG02895.hp1 others(2): Show |
intron_variant | MODIFIER | c.887+396_887+411del others(16): Show |
RNF128 | ENSG00000133135.14 | transcript | ENST00000255499.3 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chrX | 106788373 | |||||
chrX:106788381
|
T | A | 8 | a0001c0001t0002g0004a0001c0001t0002g0017a0001c0001t0002g0019others(5): Show | 9 | HG01243.hp1 HG02559.hp1 HG02630.hp2 others(6): Show |
intron_variant | MODIFIER | c.887+381T>A | RNF128 | ENSG00000133135.14 | transcript | ENST00000255499.3 | protein_coding | 4/6 | chrX | 106788381 | ||||||
chrX:106788386
|
A | ATAT | 1 | a0001c0001t0001g0031 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.887+388_887+389ins others(3): Show |
RNF128 | ENSG00000133135.14 | transcript | ENST00000255499.3 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chrX | 106788386 | |||||
chrX:106788387
|
TAA | T | 1 | a0001c0001t0001g0107 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.887+388_887+389del others(2): Show |
RNF128 | ENSG00000133135.14 | transcript | ENST00000255499.3 | protein_coding | 4/6 | chrX | 106788387 | ||||||
chrX:106788388
|
AATATATA others(2): Show |
A | 10 | a0001c0001t0002g0004a0001c0001t0002g0017a0001c0001t0002g0019others(7): Show | 11 | HG01243.hp1 HG02559.hp1 HG02622.hp2 others(8): Show |
intron_variant | MODIFIER | c.887+396_887+404del others(9): Show |
RNF128 | ENSG00000133135.14 | transcript | ENST00000255499.3 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chrX | 106788388 | |||||
chrX:106788395
|
ATT | A | 1 | a0001c0001t0002g0044 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.887+396_887+397del others(2): Show |
RNF128 | ENSG00000133135.14 | transcript | ENST00000255499.3 | protein_coding | 4/6 | chrX | 106788395 | ||||||
chrX:106788396
|
T | TAGATATA | 1 | a0001c0001t0001g0031 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.887+396_887+397ins others(7): Show |
RNF128 | ENSG00000133135.14 | transcript | ENST00000255499.3 | protein_coding | 4/6 | chrX | 106788396 | ||||||
chrX:106788397
|
T | A | 7 | a0001c0001t0001g0070a0001c0001t0001g0132a0001c0001t0001g0174others(4): Show | 8 | HG01175.hp1 HG01884.hp2 HG02145.hp1 others(5): Show |
intron_variant | MODIFIER | c.887+397T>A | RNF128 | ENSG00000133135.14 | transcript | ENST00000255499.3 | protein_coding | 4/6 | chrX | 106788397 | ||||||
chrX:106788397
|
T | G | 1 | a0001c0001t0001g0031 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.887+397T>G | RNF128 | ENSG00000133135.14 | transcript | ENST00000255499.3 | protein_coding | 4/6 | chrX | 106788397 | ||||||
chrX:106788397
|
T | TATATATA | 14 | a0001c0001t0001g0003a0001c0001t0001g0018a0001c0001t0001g0027others(11): Show | 15 | HG02109.hp1 HG02109.hp2 HG02486.hp1 others(12): Show |
intron_variant | MODIFIER | c.887+419_887+425dup others(7): Show |
RNF128 | ENSG00000133135.14 | transcript | ENST00000255499.3 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chrX | 106788397 | |||||
chrX:106788397
|
T | TATATATA others(7): Show |
1 | a0001c0001t0001g0155 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.887+412_887+425dup others(14): Show |
RNF128 | ENSG00000133135.14 | transcript | ENST00000255499.3 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chrX | 106788397 | |||||
chrX:106788397
|
T | TATATATA others(21): Show |
1 | a0001c0001t0001g0028 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.887+398_887+425dup others(28): Show |
RNF128 | ENSG00000133135.14 | transcript | ENST00000255499.3 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chrX | 106788397 | |||||
chrX:106788397
|
TATATATA | T | 1 | a0001c0001t0001g0171 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.887+419_887+425del others(7): Show |
RNF128 | ENSG00000133135.14 | transcript | ENST00000255499.3 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chrX | 106788397 | |||||
chrX:106788426
|
T | A | 3 | a0001c0001t0001g0030a0001c0001t0001g0037a0001c0001t0001g0155 | 3 | HG03471.hp1 HG06807.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.887+426T>A | RNF128 | ENSG00000133135.14 | transcript | ENST00000255499.3 | protein_coding | 4/6 | chrX | 106788426 | ||||||
chrX:106788426
|
T | TTATATAT others(19): Show |
1 | a0001c0001t0001g0122 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.887+449_887+474dup others(26): Show |
RNF128 | ENSG00000133135.14 | transcript | ENST00000255499.3 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chrX | 106788426 | |||||
chrX:106788439
|
TATTATAA others(58): Show |
T | 1 | a0001c0001t0001g0135 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.887+465_887+529del others(65): Show |
RNF128 | ENSG00000133135.14 | transcript | ENST00000255499.3 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chrX | 106788439 | |||||
chrX:106788446
|
ATT | A | 3 | a0001c0001t0001g0127a0001c0001t0001g0142a0001c0001t0001g0145 | 3 | NA19055.hp1 NA19062.hp1 NA19076.hp1 |
intron_variant | MODIFIER | c.887+447_887+448del others(2): Show |
RNF128 | ENSG00000133135.14 | transcript | ENST00000255499.3 | protein_coding | 4/6 | chrX | 106788446 | ||||||
chrX:106788497
|
AT | A | 2 | a0001c0001t0001g0060a0001c0001t0003g0130 | 2 | NA18961.hp1 NA18983.hp1 |
intron_variant | MODIFIER | c.887+499delT | RNF128 | ENSG00000133135.14 | transcript | ENST00000255499.3 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chrX | 106788497 | |||||
chrX:106788616
|
T | TATTATAT others(29): Show |
4 | a0001c0001t0001g0048a0001c0001t0001g0106a0001c0001t0001g0134others(1): Show | 4 | HG00741.hp1 HG01192.hp1 HG02647.hp1 others(1): Show |
intron_variant | MODIFIER | c.887+653_887+688dup others(36): Show |
RNF128 | ENSG00000133135.14 | transcript | ENST00000255499.3 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chrX | 106788616 | |||||
chrX:106788624
|
AT | A | 15 | a0001c0001t0002g0002a0001c0001t0002g0004a0001c0001t0002g0017others(12): Show | 17 | HG01243.hp1 HG01884.hp2 HG02145.hp1 others(14): Show |
intron_variant | MODIFIER | c.887+625delT | RNF128 | ENSG00000133135.14 | transcript | ENST00000255499.3 | protein_coding | 4/6 | chrX | 106788624 | ||||||
chrX:106788662
|
A | G | 2 | a0001c0001t0001g0049a0001c0001t0001g0050 | 2 | HG03540.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.887+662A>G | RNF128 | ENSG00000133135.14 | transcript | ENST00000255499.3 | protein_coding | 4/6 | chrX | 106788662 | ||||||
chrX:106788696
|
A | G | 1 | a0001c0001t0001g0040 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.887+696A>G | RNF128 | ENSG00000133135.14 | transcript | ENST00000255499.3 | protein_coding | 4/6 | chrX | 106788696 | ||||||
chrX:106788968
|
A | G | 1 | a0001c0001t0001g0049 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.887+968A>G | RNF128 | ENSG00000133135.14 | transcript | ENST00000255499.3 | protein_coding | 4/6 | chrX | 106788968 | ||||||
chrX:106789070
|
G | GTATATAT others(18): Show |
1 | a0001c0001t0001g0093 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.887+1086_888-1076d others(27): Show |
RNF128 | ENSG00000133135.14 | transcript | ENST00000255499.3 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chrX | 106789070 | |||||
chrX:106789086
|
G | GTA | 1 | a0001c0001t0001g0039 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.887+1091_887+1092d others(4): Show |
RNF128 | ENSG00000133135.14 | transcript | ENST00000255499.3 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chrX | 106789086 | |||||
chrX:106789095
|
ATATATAT others(2): Show |
A | 1 | a0001c0001t0001g0175 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.888-1084_888-1076d others(11): Show |
RNF128 | ENSG00000133135.14 | transcript | ENST00000255499.3 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chrX | 106789095 | |||||
chrX:106789383
|
GTA | G | 3 | a0001c0001t0001g0066a0001c0001t0001g0068a0001c0001t0001g0079 | 3 | NA18986.hp1 NA18988.hp1 NA18990.hp1 |
intron_variant | MODIFIER | c.888-795_888-794del others(2): Show |
RNF128 | ENSG00000133135.14 | transcript | ENST00000255499.3 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chrX | 106789383 | |||||
chrX:106789385
|
A | G | 32 | a0001c0001t0001g0003a0001c0001t0001g0018a0001c0001t0001g0027others(29): Show | 35 | HG01243.hp1 HG01884.hp2 HG02109.hp1 others(32): Show |
intron_variant | MODIFIER | c.888-801A>G | RNF128 | ENSG00000133135.14 | transcript | ENST00000255499.3 | protein_coding | 4/6 | chrX | 106789385 | ||||||
chrX:106789429
|
A | AGTATAAT others(26): Show |
17 | a0001c0001t0001g0003a0001c0001t0001g0018a0001c0001t0001g0027others(14): Show | 18 | HG02109.hp1 HG02109.hp2 HG02486.hp1 others(15): Show |
intron_variant | MODIFIER | c.888-752_888-751ins others(33): Show |
RNF128 | ENSG00000133135.14 | transcript | ENST00000255499.3 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chrX | 106789429 | |||||
chrX:106789429
|
A | AGTATATA others(30): Show |
159 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(156): Show | 175 | HG00140.hp1 HG00438.hp1 HG00438.hp2 others(172): Show |
intron_variant | MODIFIER | c.888-726_888-690dup others(37): Show |
RNF128 | ENSG00000133135.14 | transcript | ENST00000255499.3 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chrX | 106789429 | |||||
chrX:106789453
|
C | CTATATAA others(69): Show |
11 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0096others(8): Show | 13 | HG00280.hp1 HG00741.hp2 HG01071.hp2 others(10): Show |
intron_variant | MODIFIER | c.888-690_888-689ins others(76): Show |
RNF128 | ENSG00000133135.14 | transcript | ENST00000255499.3 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chrX | 106789453 | |||||
chrX:106789453
|
C | CTATATAA others(108): Show |
2 | a0001c0001t0001g0103a0001c0001t0001g0104 | 2 | HG00735.hp1 HG01255.hp1 |
intron_variant | MODIFIER | c.888-690_888-689ins others(115): Show |
RNF128 | ENSG00000133135.14 | transcript | ENST00000255499.3 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chrX | 106789453 | |||||
chrX:106789561
|
ATAT | A | 3 | a0001c0001t0001g0106a0001c0001t0001g0109a0001c0001t0001g0134 | 3 | HG00741.hp1 HG01081.hp2 HG01192.hp1 |
intron_variant | MODIFIER | c.888-621_888-619del others(3): Show |
RNF128 | ENSG00000133135.14 | transcript | ENST00000255499.3 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chrX | 106789561 | |||||
chrX:106789790
|
G | GC | 1 | a0001c0001t0001g0031 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.888-394dupC | RNF128 | ENSG00000133135.14 | transcript | ENST00000255499.3 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chrX | 106789790 | |||||
chrX:106789961
|
A | AT | 1 | a0001c0001t0004g0128 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.888-216dupT | RNF128 | ENSG00000133135.14 | transcript | ENST00000255499.3 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chrX | 106789961 | |||||
chrX:106789988
|
G | GC | 1 | a0001c0001t0001g0067 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.888-197dupC | RNF128 | ENSG00000133135.14 | transcript | ENST00000255499.3 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chrX | 106789988 | |||||
chrX:106790372
|
A | G | 1 | a0001c0001t0001g0045 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.984+90A>G | RNF128 | ENSG00000133135.14 | transcript | ENST00000255499.3 | protein_coding | 5/6 | chrX | 106790372 | ||||||
chrX:106790551
|
G | A | 32 | a0001c0001t0001g0003a0001c0001t0001g0018a0001c0001t0001g0027others(29): Show | 35 | HG01243.hp1 HG01884.hp2 HG02109.hp1 others(32): Show |
intron_variant | MODIFIER | c.984+269G>A | RNF128 | ENSG00000133135.14 | transcript | ENST00000255499.3 | protein_coding | 5/6 | chrX | 106790551 | ||||||
chrX:106790583
|
C | CA | 1 | a0001c0001t0001g0067 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.984+304dupA | RNF128 | ENSG00000133135.14 | transcript | ENST00000255499.3 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chrX | 106790583 | |||||
chrX:106790662
|
A | T | 3 | a0001c0001t0001g0183a0001c0001t0001g0184a0001c0001t0001g0185 | 3 | HG02559.hp2 HG02897.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.984+380A>T | RNF128 | ENSG00000133135.14 | transcript | ENST00000255499.3 | protein_coding | 5/6 | chrX | 106790662 | ||||||
chrX:106791316
|
G | A | 1 | a0001c0001t0001g0188 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.1153+82G>A | RNF128 | ENSG00000133135.14 | transcript | ENST00000255499.3 | protein_coding | 6/6 | chrX | 106791316 | ||||||
chrX:106791463
|
A | C | 9 | a0001c0001t0002g0017a0001c0001t0002g0019a0001c0001t0002g0020others(6): Show | 9 | HG01243.hp1 HG02559.hp1 HG02622.hp2 others(6): Show |
intron_variant | MODIFIER | c.1153+229A>C | RNF128 | ENSG00000133135.14 | transcript | ENST00000255499.3 | protein_coding | 6/6 | chrX | 106791463 | ||||||
chrX:106791587
|
TA | T | 1 | a0001c0001t0001g0067 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.1153+356delA | RNF128 | ENSG00000133135.14 | transcript | ENST00000255499.3 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chrX | 106791587 | |||||
chrX:106792125
|
A | G | 32 | a0001c0001t0001g0003a0001c0001t0001g0018a0001c0001t0001g0027others(29): Show | 35 | HG01243.hp1 HG01884.hp2 HG02109.hp1 others(32): Show |
intron_variant | MODIFIER | c.1153+891A>G | RNF128 | ENSG00000133135.14 | transcript | ENST00000255499.3 | protein_coding | 6/6 | chrX | 106792125 | ||||||
chrX:106792944
|
A | G | 1 | a0001c0001t0001g0092 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.1153+1710A>G | RNF128 | ENSG00000133135.14 | transcript | ENST00000255499.3 | protein_coding | 6/6 | chrX | 106792944 | ||||||
chrX:106792951
|
G | A | 1 | a0001c0001t0002g0044 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.1153+1717G>A | RNF128 | ENSG00000133135.14 | transcript | ENST00000255499.3 | protein_coding | 6/6 | chrX | 106792951 | ||||||
chrX:106793292
|
C | T | 1 | a0001c0001t0005g0052 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.1153+2058C>T | RNF128 | ENSG00000133135.14 | transcript | ENST00000255499.3 | protein_coding | 6/6 | chrX | 106793292 | ||||||
chrX:106793569
|
C | T | 15 | a0001c0001t0002g0002a0001c0001t0002g0004a0001c0001t0002g0017others(12): Show | 17 | HG01243.hp1 HG01884.hp2 HG02145.hp1 others(14): Show |
intron_variant | MODIFIER | c.1154-2011C>T | RNF128 | ENSG00000133135.14 | transcript | ENST00000255499.3 | protein_coding | 6/6 | chrX | 106793569 | ||||||
chrX:106794188
|
G | A | 5 | a0001c0001t0001g0060a0001c0001t0001g0070a0001c0001t0001g0084others(2): Show | 5 | HG00140.hp1 HG01175.hp1 HG02155.hp1 others(2): Show |
intron_variant | MODIFIER | c.1154-1392G>A | RNF128 | ENSG00000133135.14 | transcript | ENST00000255499.3 | protein_coding | 6/6 | chrX | 106794188 | ||||||
chrX:106794237
|
A | G | 2 | a0001c0001t0002g0025a0001c0001t0002g0026 | 2 | HG02145.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.1154-1343A>G | RNF128 | ENSG00000133135.14 | transcript | ENST00000255499.3 | protein_coding | 6/6 | chrX | 106794237 | ||||||
chrX:106794640
|
A | AC | 1 | a0001c0001t0001g0180 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.1154-938dupC | RNF128 | ENSG00000133135.14 | transcript | ENST00000255499.3 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chrX | 106794640 | |||||
chrX:106794806
|
T | G | 189 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0005others(186): Show | 208 | HG00140.hp1 HG00280.hp1 HG00438.hp1 others(205): Show |
intron_variant | MODIFIER | c.1154-774T>G | RNF128 | ENSG00000133135.14 | transcript | ENST00000255499.3 | protein_coding | 6/6 | chrX | 106794806 | ||||||
chrX:106794976
|
A | AAACTAAT others(30): Show |
1 | a0001c0001t0001g0046 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.1154-604_1154-603i others(39): Show |
RNF128 | ENSG00000133135.14 | transcript | ENST00000255499.3 | protein_coding | 6/6 | chrX | 106794976 | ||||||
chrX:106794977
|
G | C | 1 | a0001c0001t0001g0046 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.1154-603G>C | RNF128 | ENSG00000133135.14 | transcript | ENST00000255499.3 | protein_coding | 6/6 | chrX | 106794977 |