geneid | 29057 |
---|---|
ensemblid | ENSG00000268350.8 |
hgncid | 30114 |
symbol | FAM156A |
name | family with sequence similarity 156 member A |
refseq_nuc | NM_001387706.1 |
refseq_prot | NP_001374635.1 |
ensembl_nuc | ENST00000622447.5 |
ensembl_prot | ENSP00000482142.1 |
mane_status | MANE Select |
chr | chrX |
start | 52947254 |
end | 52958518 |
strand | - |
ver | v1.2 |
region | chrX:52947254-52958518 |
region5000 | chrX:52942254-52963518 |
regionname0 | FAM156A_chrX_52947254_52958518 |
regionname5000 | FAM156A_chrX_52942254_52963518 |
ahapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 0/0 | 213 | 156 | 44 | 40 | 48 | 5 | 19 | 36 | FAM156A_chrX_52942254_52963518 | FAM156A | copy fasta | chrX | 52942254 | 52963518 |
a0002 | 0/0 | 213 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | FAM156A_chrX_52942254_52963518 | FAM156A | copy fasta | chrX | 52942254 | 52963518 |
a0003 | 0/0 | 117 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | FAM156A_chrX_52942254_52963518 | FAM156A | copy fasta | chrX | 52942254 | 52963518 |
a0004 | 0/0 | 117 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | FAM156A_chrX_52942254_52963518 | FAM156A | copy fasta | chrX | 52942254 | 52963518 |
a0005 | 0/0 | 177 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | FAM156A_chrX_52942254_52963518 | FAM156A | copy fasta | chrX | 52942254 | 52963518 |
a0006 | 0/0 | 39 | 1 | 0 | 0 | 0 | 1 | 0 | 0 | FAM156A_chrX_52942254_52963518 | FAM156A | copy fasta | chrX | 52942254 | 52963518 |
chapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
c0001 | 0/0 | 642 | 156 | 44 | 40 | 48 | 5 | 19 | FAM156A_chrX_52942254_52963518 | FAM156A | copy fasta | chrX | 52942254 | 52963518 |
c0002 | 0/0 | 642 | 1 | 0 | 0 | 0 | 1 | 0 | FAM156A_chrX_52942254_52963518 | FAM156A | copy fasta | chrX | 52942254 | 52963518 |
c0003 | 0/0 | 642 | 1 | 1 | 0 | 0 | 0 | 0 | FAM156A_chrX_52942254_52963518 | FAM156A | copy fasta | chrX | 52942254 | 52963518 |
c0004 | 0/0 | 643 | 1 | 1 | 0 | 0 | 0 | 0 | FAM156A_chrX_52942254_52963518 | FAM156A | copy fasta | chrX | 52942254 | 52963518 |
c0005 | 0/0 | 643 | 1 | 0 | 0 | 1 | 0 | 0 | FAM156A_chrX_52942254_52963518 | FAM156A | copy fasta | chrX | 52942254 | 52963518 |
c0006 | 0/0 | 643 | 1 | 0 | 0 | 1 | 0 | 0 | FAM156A_chrX_52942254_52963518 | FAM156A | copy fasta | chrX | 52942254 | 52963518 |
thapid | grch38chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
t0001 | 0/0 | 3150 | 91 | 31 | 25 | 26 | 1 | 8 | FAM156A_chrX_52942254_52963518 | FAM156A | copy fasta | chrX | 52942254 | 52963518 |
t0002 | 0/0 | 3150 | 36 | 3 | 8 | 17 | 3 | 5 | FAM156A_chrX_52942254_52963518 | FAM156A | copy fasta | chrX | 52942254 | 52963518 |
t0003 | 0/0 | 3149 | 10 | 3 | 4 | 0 | 2 | 1 | FAM156A_chrX_52942254_52963518 | FAM156A | copy fasta | chrX | 52942254 | 52963518 |
t0004 | 0/0 | 3150 | 4 | 3 | 1 | 0 | 0 | 0 | FAM156A_chrX_52942254_52963518 | FAM156A | copy fasta | chrX | 52942254 | 52963518 |
t0005 | 0/0 | 3146 | 2 | 0 | 0 | 2 | 0 | 0 | FAM156A_chrX_52942254_52963518 | FAM156A | copy fasta | chrX | 52942254 | 52963518 |
t0006 | 0/0 | 3158 | 1 | 0 | 1 | 0 | 0 | 0 | FAM156A_chrX_52942254_52963518 | FAM156A | copy fasta | chrX | 52942254 | 52963518 |
t0007 | 0/0 | 3150 | 1 | 0 | 0 | 1 | 0 | 0 | FAM156A_chrX_52942254_52963518 | FAM156A | copy fasta | chrX | 52942254 | 52963518 |
t0008 | 0/0 | 3149 | 1 | 1 | 0 | 0 | 0 | 0 | FAM156A_chrX_52942254_52963518 | FAM156A | copy fasta | chrX | 52942254 | 52963518 |
t0009 | 0/0 | 3151 | 1 | 1 | 0 | 0 | 0 | 0 | FAM156A_chrX_52942254_52963518 | FAM156A | copy fasta | chrX | 52942254 | 52963518 |
t0010 | 0/0 | 3150 | 1 | 1 | 0 | 0 | 0 | 0 | FAM156A_chrX_52942254_52963518 | FAM156A | copy fasta | chrX | 52942254 | 52963518 |
t0011 | 0/0 | 3150 | 1 | 1 | 0 | 0 | 0 | 0 | FAM156A_chrX_52942254_52963518 | FAM156A | copy fasta | chrX | 52942254 | 52963518 |
t0012 | 0/0 | 3148 | 1 | 0 | 0 | 0 | 0 | 1 | FAM156A_chrX_52942254_52963518 | FAM156A | copy fasta | chrX | 52942254 | 52963518 |
t0013 | 0/0 | 3150 | 1 | 0 | 0 | 0 | 0 | 1 | FAM156A_chrX_52942254_52963518 | FAM156A | copy fasta | chrX | 52942254 | 52963518 |
t0014 | 0/0 | 3151 | 1 | 0 | 0 | 1 | 0 | 0 | FAM156A_chrX_52942254_52963518 | FAM156A | copy fasta | chrX | 52942254 | 52963518 |
t0015 | 0/0 | 3152 | 1 | 0 | 1 | 0 | 0 | 0 | FAM156A_chrX_52942254_52963518 | FAM156A | copy fasta | chrX | 52942254 | 52963518 |
t0016 | 0/0 | 3150 | 1 | 0 | 0 | 1 | 0 | 0 | FAM156A_chrX_52942254_52963518 | FAM156A | copy fasta | chrX | 52942254 | 52963518 |
t0017 | 0/0 | 3150 | 1 | 0 | 0 | 0 | 0 | 1 | FAM156A_chrX_52942254_52963518 | FAM156A | copy fasta | chrX | 52942254 | 52963518 |
t0018 | 0/0 | 3151 | 1 | 1 | 0 | 0 | 0 | 0 | FAM156A_chrX_52942254_52963518 | FAM156A | copy fasta | chrX | 52942254 | 52963518 |
t0019 | 0/0 | 3151 | 1 | 0 | 0 | 0 | 0 | 1 | FAM156A_chrX_52942254_52963518 | FAM156A | copy fasta | chrX | 52942254 | 52963518 |
t0020 | 0/0 | 3145 | 1 | 0 | 0 | 1 | 0 | 0 | FAM156A_chrX_52942254_52963518 | FAM156A | copy fasta | chrX | 52942254 | 52963518 |
t0021 | 0/0 | 3150 | 1 | 0 | 0 | 0 | 0 | 1 | FAM156A_chrX_52942254_52963518 | FAM156A | copy fasta | chrX | 52942254 | 52963518 |
t0022 | 0/0 | 3148 | 1 | 1 | 0 | 0 | 0 | 0 | FAM156A_chrX_52942254_52963518 | FAM156A | copy fasta | chrX | 52942254 | 52963518 |
t0023 | 0/0 | 3150 | 1 | 0 | 0 | 1 | 0 | 0 | FAM156A_chrX_52942254_52963518 | FAM156A | copy fasta | chrX | 52942254 | 52963518 |
ghapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
g0001 | 0/0 | 12 | 6 | 1 | 4 | 0 | 1 | FAM156A_chrX_52942254_52963518 | FAM156A | chrX | 52942254 | 52963518 |
g0002 | 0/0 | 11 | 0 | 4 | 5 | 0 | 2 | FAM156A_chrX_52942254_52963518 | FAM156A | chrX | 52942254 | 52963518 |
g0003 | 0/0 | 11 | 0 | 3 | 5 | 0 | 3 | FAM156A_chrX_52942254_52963518 | FAM156A | chrX | 52942254 | 52963518 |
g0004 | 0/0 | 5 | 0 | 2 | 1 | 1 | 1 | FAM156A_chrX_52942254_52963518 | FAM156A | chrX | 52942254 | 52963518 |
g0005 | 0/0 | 4 | 0 | 4 | 0 | 0 | 0 | FAM156A_chrX_52942254_52963518 | FAM156A | chrX | 52942254 | 52963518 |
g0006 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | FAM156A_chrX_52942254_52963518 | FAM156A | chrX | 52942254 | 52963518 |
g0007 | 0/0 | 4 | 2 | 1 | 1 | 0 | 0 | FAM156A_chrX_52942254_52963518 | FAM156A | chrX | 52942254 | 52963518 |
g0008 | 0/0 | 3 | 0 | 1 | 2 | 0 | 0 | FAM156A_chrX_52942254_52963518 | FAM156A | chrX | 52942254 | 52963518 |
g0009 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FAM156A_chrX_52942254_52963518 | FAM156A | chrX | 52942254 | 52963518 |
g0010 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | FAM156A_chrX_52942254_52963518 | FAM156A | chrX | 52942254 | 52963518 |
g0011 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FAM156A_chrX_52942254_52963518 | FAM156A | chrX | 52942254 | 52963518 |
g0012 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FAM156A_chrX_52942254_52963518 | FAM156A | chrX | 52942254 | 52963518 |
g0013 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FAM156A_chrX_52942254_52963518 | FAM156A | chrX | 52942254 | 52963518 |
g0014 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FAM156A_chrX_52942254_52963518 | FAM156A | chrX | 52942254 | 52963518 |
g0015 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | FAM156A_chrX_52942254_52963518 | FAM156A | chrX | 52942254 | 52963518 |
g0016 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FAM156A_chrX_52942254_52963518 | FAM156A | chrX | 52942254 | 52963518 |
g0017 | 0/0 | 2 | 1 | 0 | 1 | 0 | 0 | FAM156A_chrX_52942254_52963518 | FAM156A | chrX | 52942254 | 52963518 |
g0018 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM156A_chrX_52942254_52963518 | FAM156A | chrX | 52942254 | 52963518 |
g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM156A_chrX_52942254_52963518 | FAM156A | chrX | 52942254 | 52963518 |
g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM156A_chrX_52942254_52963518 | FAM156A | chrX | 52942254 | 52963518 |
g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM156A_chrX_52942254_52963518 | FAM156A | chrX | 52942254 | 52963518 |
g0022 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM156A_chrX_52942254_52963518 | FAM156A | chrX | 52942254 | 52963518 |
g0023 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM156A_chrX_52942254_52963518 | FAM156A | chrX | 52942254 | 52963518 |
g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM156A_chrX_52942254_52963518 | FAM156A | chrX | 52942254 | 52963518 |
g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM156A_chrX_52942254_52963518 | FAM156A | chrX | 52942254 | 52963518 |
g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM156A_chrX_52942254_52963518 | FAM156A | chrX | 52942254 | 52963518 |
g0027 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM156A_chrX_52942254_52963518 | FAM156A | chrX | 52942254 | 52963518 |
g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM156A_chrX_52942254_52963518 | FAM156A | chrX | 52942254 | 52963518 |
g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM156A_chrX_52942254_52963518 | FAM156A | chrX | 52942254 | 52963518 |
g0030 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM156A_chrX_52942254_52963518 | FAM156A | chrX | 52942254 | 52963518 |
g0031 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM156A_chrX_52942254_52963518 | FAM156A | chrX | 52942254 | 52963518 |
g0032 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM156A_chrX_52942254_52963518 | FAM156A | chrX | 52942254 | 52963518 |
g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM156A_chrX_52942254_52963518 | FAM156A | chrX | 52942254 | 52963518 |
g0034 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM156A_chrX_52942254_52963518 | FAM156A | chrX | 52942254 | 52963518 |
g0035 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM156A_chrX_52942254_52963518 | FAM156A | chrX | 52942254 | 52963518 |
g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM156A_chrX_52942254_52963518 | FAM156A | chrX | 52942254 | 52963518 |
g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM156A_chrX_52942254_52963518 | FAM156A | chrX | 52942254 | 52963518 |
g0038 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM156A_chrX_52942254_52963518 | FAM156A | chrX | 52942254 | 52963518 |
g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM156A_chrX_52942254_52963518 | FAM156A | chrX | 52942254 | 52963518 |
g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM156A_chrX_52942254_52963518 | FAM156A | chrX | 52942254 | 52963518 |
g0041 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM156A_chrX_52942254_52963518 | FAM156A | chrX | 52942254 | 52963518 |
g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM156A_chrX_52942254_52963518 | FAM156A | chrX | 52942254 | 52963518 |
g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM156A_chrX_52942254_52963518 | FAM156A | chrX | 52942254 | 52963518 |
g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM156A_chrX_52942254_52963518 | FAM156A | chrX | 52942254 | 52963518 |
g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM156A_chrX_52942254_52963518 | FAM156A | chrX | 52942254 | 52963518 |
g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM156A_chrX_52942254_52963518 | FAM156A | chrX | 52942254 | 52963518 |
g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM156A_chrX_52942254_52963518 | FAM156A | chrX | 52942254 | 52963518 |
g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM156A_chrX_52942254_52963518 | FAM156A | chrX | 52942254 | 52963518 |
g0049 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM156A_chrX_52942254_52963518 | FAM156A | chrX | 52942254 | 52963518 |
g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM156A_chrX_52942254_52963518 | FAM156A | chrX | 52942254 | 52963518 |
g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM156A_chrX_52942254_52963518 | FAM156A | chrX | 52942254 | 52963518 |
g0052 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM156A_chrX_52942254_52963518 | FAM156A | chrX | 52942254 | 52963518 |
g0053 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM156A_chrX_52942254_52963518 | FAM156A | chrX | 52942254 | 52963518 |
g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM156A_chrX_52942254_52963518 | FAM156A | chrX | 52942254 | 52963518 |
g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM156A_chrX_52942254_52963518 | FAM156A | chrX | 52942254 | 52963518 |
g0056 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM156A_chrX_52942254_52963518 | FAM156A | chrX | 52942254 | 52963518 |
g0057 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM156A_chrX_52942254_52963518 | FAM156A | chrX | 52942254 | 52963518 |
g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM156A_chrX_52942254_52963518 | FAM156A | chrX | 52942254 | 52963518 |
g0059 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM156A_chrX_52942254_52963518 | FAM156A | chrX | 52942254 | 52963518 |
g0060 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM156A_chrX_52942254_52963518 | FAM156A | chrX | 52942254 | 52963518 |
g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM156A_chrX_52942254_52963518 | FAM156A | chrX | 52942254 | 52963518 |
g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM156A_chrX_52942254_52963518 | FAM156A | chrX | 52942254 | 52963518 |
g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM156A_chrX_52942254_52963518 | FAM156A | chrX | 52942254 | 52963518 |
g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM156A_chrX_52942254_52963518 | FAM156A | chrX | 52942254 | 52963518 |
g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM156A_chrX_52942254_52963518 | FAM156A | chrX | 52942254 | 52963518 |
g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM156A_chrX_52942254_52963518 | FAM156A | chrX | 52942254 | 52963518 |
g0067 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM156A_chrX_52942254_52963518 | FAM156A | chrX | 52942254 | 52963518 |
g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM156A_chrX_52942254_52963518 | FAM156A | chrX | 52942254 | 52963518 |
g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM156A_chrX_52942254_52963518 | FAM156A | chrX | 52942254 | 52963518 |
g0070 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM156A_chrX_52942254_52963518 | FAM156A | chrX | 52942254 | 52963518 |
g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM156A_chrX_52942254_52963518 | FAM156A | chrX | 52942254 | 52963518 |
g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM156A_chrX_52942254_52963518 | FAM156A | chrX | 52942254 | 52963518 |
g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM156A_chrX_52942254_52963518 | FAM156A | chrX | 52942254 | 52963518 |
g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM156A_chrX_52942254_52963518 | FAM156A | chrX | 52942254 | 52963518 |
g0075 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM156A_chrX_52942254_52963518 | FAM156A | chrX | 52942254 | 52963518 |
g0076 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM156A_chrX_52942254_52963518 | FAM156A | chrX | 52942254 | 52963518 |
g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM156A_chrX_52942254_52963518 | FAM156A | chrX | 52942254 | 52963518 |
g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM156A_chrX_52942254_52963518 | FAM156A | chrX | 52942254 | 52963518 |
g0079 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM156A_chrX_52942254_52963518 | FAM156A | chrX | 52942254 | 52963518 |
g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM156A_chrX_52942254_52963518 | FAM156A | chrX | 52942254 | 52963518 |
g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM156A_chrX_52942254_52963518 | FAM156A | chrX | 52942254 | 52963518 |
g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM156A_chrX_52942254_52963518 | FAM156A | chrX | 52942254 | 52963518 |
g0083 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM156A_chrX_52942254_52963518 | FAM156A | chrX | 52942254 | 52963518 |
g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM156A_chrX_52942254_52963518 | FAM156A | chrX | 52942254 | 52963518 |
g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM156A_chrX_52942254_52963518 | FAM156A | chrX | 52942254 | 52963518 |
g0086 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM156A_chrX_52942254_52963518 | FAM156A | chrX | 52942254 | 52963518 |
g0087 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM156A_chrX_52942254_52963518 | FAM156A | chrX | 52942254 | 52963518 |
g0088 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM156A_chrX_52942254_52963518 | FAM156A | chrX | 52942254 | 52963518 |
g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM156A_chrX_52942254_52963518 | FAM156A | chrX | 52942254 | 52963518 |
g0090 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM156A_chrX_52942254_52963518 | FAM156A | chrX | 52942254 | 52963518 |
g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM156A_chrX_52942254_52963518 | FAM156A | chrX | 52942254 | 52963518 |
g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM156A_chrX_52942254_52963518 | FAM156A | chrX | 52942254 | 52963518 |
g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM156A_chrX_52942254_52963518 | FAM156A | chrX | 52942254 | 52963518 |
g0094 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM156A_chrX_52942254_52963518 | FAM156A | chrX | 52942254 | 52963518 |
g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM156A_chrX_52942254_52963518 | FAM156A | chrX | 52942254 | 52963518 |
g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM156A_chrX_52942254_52963518 | FAM156A | chrX | 52942254 | 52963518 |
g0097 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM156A_chrX_52942254_52963518 | FAM156A | chrX | 52942254 | 52963518 |
g0098 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM156A_chrX_52942254_52963518 | FAM156A | chrX | 52942254 | 52963518 |
g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM156A_chrX_52942254_52963518 | FAM156A | chrX | 52942254 | 52963518 |
g0100 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM156A_chrX_52942254_52963518 | FAM156A | chrX | 52942254 | 52963518 |
g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM156A_chrX_52942254_52963518 | FAM156A | chrX | 52942254 | 52963518 |
g0102 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM156A_chrX_52942254_52963518 | FAM156A | chrX | 52942254 | 52963518 |
g0103 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM156A_chrX_52942254_52963518 | FAM156A | chrX | 52942254 | 52963518 |
g0104 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM156A_chrX_52942254_52963518 | FAM156A | chrX | 52942254 | 52963518 |
g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM156A_chrX_52942254_52963518 | FAM156A | chrX | 52942254 | 52963518 |
g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM156A_chrX_52942254_52963518 | FAM156A | chrX | 52942254 | 52963518 |
achapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 0/0 | 642 | 156 | 44 | 40 | 48 | 5 | 19 | FAM156A_chrX_52942254_52963518 | FAM156A | copy fasta | chrX | 52942254 | 52963518 |
a0002c0003 | 0/0 | 642 | 1 | 1 | 0 | 0 | 0 | 0 | FAM156A_chrX_52942254_52963518 | FAM156A | copy fasta | chrX | 52942254 | 52963518 |
a0003c0004 | 0/0 | 643 | 1 | 1 | 0 | 0 | 0 | 0 | FAM156A_chrX_52942254_52963518 | FAM156A | copy fasta | chrX | 52942254 | 52963518 |
a0004c0005 | 0/0 | 643 | 1 | 0 | 0 | 1 | 0 | 0 | FAM156A_chrX_52942254_52963518 | FAM156A | copy fasta | chrX | 52942254 | 52963518 |
a0005c0006 | 0/0 | 643 | 1 | 0 | 0 | 1 | 0 | 0 | FAM156A_chrX_52942254_52963518 | FAM156A | copy fasta | chrX | 52942254 | 52963518 |
a0006c0002 | 0/0 | 642 | 1 | 0 | 0 | 0 | 1 | 0 | FAM156A_chrX_52942254_52963518 | FAM156A | copy fasta | chrX | 52942254 | 52963518 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 0/0 | 3791 | 90 | 31 | 25 | 26 | 0 | 8 | FAM156A_chrX_52942254_52963518 | FAM156A | copy fasta | chrX | 52942254 | 52963518 |
a0001c0001t0002 | 0/0 | 3791 | 34 | 2 | 8 | 16 | 3 | 5 | FAM156A_chrX_52942254_52963518 | FAM156A | copy fasta | chrX | 52942254 | 52963518 |
a0001c0001t0003 | 0/0 | 3790 | 10 | 3 | 4 | 0 | 2 | 1 | FAM156A_chrX_52942254_52963518 | FAM156A | copy fasta | chrX | 52942254 | 52963518 |
a0001c0001t0004 | 0/0 | 3791 | 4 | 3 | 1 | 0 | 0 | 0 | FAM156A_chrX_52942254_52963518 | FAM156A | copy fasta | chrX | 52942254 | 52963518 |
a0001c0001t0005 | 0/0 | 3787 | 2 | 0 | 0 | 2 | 0 | 0 | FAM156A_chrX_52942254_52963518 | FAM156A | copy fasta | chrX | 52942254 | 52963518 |
a0001c0001t0006 | 0/0 | 3799 | 1 | 0 | 1 | 0 | 0 | 0 | FAM156A_chrX_52942254_52963518 | FAM156A | copy fasta | chrX | 52942254 | 52963518 |
a0001c0001t0007 | 0/0 | 3791 | 1 | 0 | 0 | 1 | 0 | 0 | FAM156A_chrX_52942254_52963518 | FAM156A | copy fasta | chrX | 52942254 | 52963518 |
a0001c0001t0008 | 0/0 | 3790 | 1 | 1 | 0 | 0 | 0 | 0 | FAM156A_chrX_52942254_52963518 | FAM156A | copy fasta | chrX | 52942254 | 52963518 |
a0001c0001t0009 | 0/0 | 3792 | 1 | 1 | 0 | 0 | 0 | 0 | FAM156A_chrX_52942254_52963518 | FAM156A | copy fasta | chrX | 52942254 | 52963518 |
a0001c0001t0010 | 0/0 | 3791 | 1 | 1 | 0 | 0 | 0 | 0 | FAM156A_chrX_52942254_52963518 | FAM156A | copy fasta | chrX | 52942254 | 52963518 |
a0001c0001t0011 | 0/0 | 3791 | 1 | 1 | 0 | 0 | 0 | 0 | FAM156A_chrX_52942254_52963518 | FAM156A | copy fasta | chrX | 52942254 | 52963518 |
a0001c0001t0012 | 0/0 | 3789 | 1 | 0 | 0 | 0 | 0 | 1 | FAM156A_chrX_52942254_52963518 | FAM156A | copy fasta | chrX | 52942254 | 52963518 |
a0001c0001t0013 | 0/0 | 3791 | 1 | 0 | 0 | 0 | 0 | 1 | FAM156A_chrX_52942254_52963518 | FAM156A | copy fasta | chrX | 52942254 | 52963518 |
a0001c0001t0015 | 0/0 | 3793 | 1 | 0 | 1 | 0 | 0 | 0 | FAM156A_chrX_52942254_52963518 | FAM156A | copy fasta | chrX | 52942254 | 52963518 |
a0001c0001t0016 | 0/0 | 3791 | 1 | 0 | 0 | 1 | 0 | 0 | FAM156A_chrX_52942254_52963518 | FAM156A | copy fasta | chrX | 52942254 | 52963518 |
a0001c0001t0017 | 0/0 | 3791 | 1 | 0 | 0 | 0 | 0 | 1 | FAM156A_chrX_52942254_52963518 | FAM156A | copy fasta | chrX | 52942254 | 52963518 |
a0001c0001t0019 | 0/0 | 3792 | 1 | 0 | 0 | 0 | 0 | 1 | FAM156A_chrX_52942254_52963518 | FAM156A | copy fasta | chrX | 52942254 | 52963518 |
a0001c0001t0020 | 0/0 | 3786 | 1 | 0 | 0 | 1 | 0 | 0 | FAM156A_chrX_52942254_52963518 | FAM156A | copy fasta | chrX | 52942254 | 52963518 |
a0001c0001t0021 | 0/0 | 3791 | 1 | 0 | 0 | 0 | 0 | 1 | FAM156A_chrX_52942254_52963518 | FAM156A | copy fasta | chrX | 52942254 | 52963518 |
a0001c0001t0022 | 0/0 | 3789 | 1 | 1 | 0 | 0 | 0 | 0 | FAM156A_chrX_52942254_52963518 | FAM156A | copy fasta | chrX | 52942254 | 52963518 |
a0001c0001t0023 | 0/0 | 3791 | 1 | 0 | 0 | 1 | 0 | 0 | FAM156A_chrX_52942254_52963518 | FAM156A | copy fasta | chrX | 52942254 | 52963518 |
a0002c0003t0002 | 0/0 | 3791 | 1 | 1 | 0 | 0 | 0 | 0 | FAM156A_chrX_52942254_52963518 | FAM156A | copy fasta | chrX | 52942254 | 52963518 |
a0003c0004t0018 | 0/0 | 3793 | 1 | 1 | 0 | 0 | 0 | 0 | FAM156A_chrX_52942254_52963518 | FAM156A | copy fasta | chrX | 52942254 | 52963518 |
a0004c0005t0002 | 0/0 | 3792 | 1 | 0 | 0 | 1 | 0 | 0 | FAM156A_chrX_52942254_52963518 | FAM156A | copy fasta | chrX | 52942254 | 52963518 |
a0005c0006t0014 | 0/0 | 3793 | 1 | 0 | 0 | 1 | 0 | 0 | FAM156A_chrX_52942254_52963518 | FAM156A | copy fasta | chrX | 52942254 | 52963518 |
a0006c0002t0001 | 0/0 | 3791 | 1 | 0 | 0 | 0 | 1 | 0 | FAM156A_chrX_52942254_52963518 | FAM156A | copy fasta | chrX | 52942254 | 52963518 |
actghapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0001 | 0/0 | 12 | 6 | 1 | 4 | 0 | 1 | FAM156A_chrX_52942254_52963518 | FAM156A | chrX | 52942254 | 52963518 |
a0001c0001t0001g0002 | 0/0 | 11 | 0 | 4 | 5 | 0 | 2 | FAM156A_chrX_52942254_52963518 | FAM156A | chrX | 52942254 | 52963518 |
a0001c0001t0001g0005 | 0/0 | 4 | 0 | 4 | 0 | 0 | 0 | FAM156A_chrX_52942254_52963518 | FAM156A | chrX | 52942254 | 52963518 |
a0001c0001t0001g0006 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | FAM156A_chrX_52942254_52963518 | FAM156A | chrX | 52942254 | 52963518 |
a0001c0001t0001g0007 | 0/0 | 4 | 2 | 1 | 1 | 0 | 0 | FAM156A_chrX_52942254_52963518 | FAM156A | chrX | 52942254 | 52963518 |
a0001c0001t0001g0009 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FAM156A_chrX_52942254_52963518 | FAM156A | chrX | 52942254 | 52963518 |
a0001c0001t0001g0010 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | FAM156A_chrX_52942254_52963518 | FAM156A | chrX | 52942254 | 52963518 |
a0001c0001t0001g0011 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FAM156A_chrX_52942254_52963518 | FAM156A | chrX | 52942254 | 52963518 |
a0001c0001t0001g0012 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FAM156A_chrX_52942254_52963518 | FAM156A | chrX | 52942254 | 52963518 |
a0001c0001t0001g0013 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FAM156A_chrX_52942254_52963518 | FAM156A | chrX | 52942254 | 52963518 |
a0001c0001t0001g0014 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FAM156A_chrX_52942254_52963518 | FAM156A | chrX | 52942254 | 52963518 |
a0001c0001t0001g0015 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | FAM156A_chrX_52942254_52963518 | FAM156A | chrX | 52942254 | 52963518 |
a0001c0001t0001g0016 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FAM156A_chrX_52942254_52963518 | FAM156A | chrX | 52942254 | 52963518 |
a0001c0001t0001g0017 | 0/0 | 2 | 1 | 0 | 1 | 0 | 0 | FAM156A_chrX_52942254_52963518 | FAM156A | chrX | 52942254 | 52963518 |
a0001c0001t0001g0022 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM156A_chrX_52942254_52963518 | FAM156A | chrX | 52942254 | 52963518 |
a0001c0001t0001g0023 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM156A_chrX_52942254_52963518 | FAM156A | chrX | 52942254 | 52963518 |
a0001c0001t0001g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM156A_chrX_52942254_52963518 | FAM156A | chrX | 52942254 | 52963518 |
a0001c0001t0001g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM156A_chrX_52942254_52963518 | FAM156A | chrX | 52942254 | 52963518 |
a0001c0001t0001g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM156A_chrX_52942254_52963518 | FAM156A | chrX | 52942254 | 52963518 |
a0001c0001t0001g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM156A_chrX_52942254_52963518 | FAM156A | chrX | 52942254 | 52963518 |
a0001c0001t0001g0031 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM156A_chrX_52942254_52963518 | FAM156A | chrX | 52942254 | 52963518 |
a0001c0001t0001g0032 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM156A_chrX_52942254_52963518 | FAM156A | chrX | 52942254 | 52963518 |
a0001c0001t0001g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM156A_chrX_52942254_52963518 | FAM156A | chrX | 52942254 | 52963518 |
a0001c0001t0001g0034 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM156A_chrX_52942254_52963518 | FAM156A | chrX | 52942254 | 52963518 |
a0001c0001t0001g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM156A_chrX_52942254_52963518 | FAM156A | chrX | 52942254 | 52963518 |
a0001c0001t0001g0038 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM156A_chrX_52942254_52963518 | FAM156A | chrX | 52942254 | 52963518 |
a0001c0001t0001g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM156A_chrX_52942254_52963518 | FAM156A | chrX | 52942254 | 52963518 |
a0001c0001t0001g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM156A_chrX_52942254_52963518 | FAM156A | chrX | 52942254 | 52963518 |
a0001c0001t0001g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM156A_chrX_52942254_52963518 | FAM156A | chrX | 52942254 | 52963518 |
a0001c0001t0001g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM156A_chrX_52942254_52963518 | FAM156A | chrX | 52942254 | 52963518 |
a0001c0001t0001g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM156A_chrX_52942254_52963518 | FAM156A | chrX | 52942254 | 52963518 |
a0001c0001t0001g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM156A_chrX_52942254_52963518 | FAM156A | chrX | 52942254 | 52963518 |
a0001c0001t0001g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM156A_chrX_52942254_52963518 | FAM156A | chrX | 52942254 | 52963518 |
a0001c0001t0001g0049 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM156A_chrX_52942254_52963518 | FAM156A | chrX | 52942254 | 52963518 |
a0001c0001t0001g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM156A_chrX_52942254_52963518 | FAM156A | chrX | 52942254 | 52963518 |
a0001c0001t0001g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM156A_chrX_52942254_52963518 | FAM156A | chrX | 52942254 | 52963518 |
a0001c0001t0001g0052 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM156A_chrX_52942254_52963518 | FAM156A | chrX | 52942254 | 52963518 |
a0001c0001t0001g0053 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM156A_chrX_52942254_52963518 | FAM156A | chrX | 52942254 | 52963518 |
a0001c0001t0001g0057 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM156A_chrX_52942254_52963518 | FAM156A | chrX | 52942254 | 52963518 |
a0001c0001t0001g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM156A_chrX_52942254_52963518 | FAM156A | chrX | 52942254 | 52963518 |
a0001c0001t0001g0070 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM156A_chrX_52942254_52963518 | FAM156A | chrX | 52942254 | 52963518 |
a0001c0001t0001g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM156A_chrX_52942254_52963518 | FAM156A | chrX | 52942254 | 52963518 |
a0001c0001t0001g0075 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM156A_chrX_52942254_52963518 | FAM156A | chrX | 52942254 | 52963518 |
a0001c0001t0001g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM156A_chrX_52942254_52963518 | FAM156A | chrX | 52942254 | 52963518 |
a0001c0001t0001g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM156A_chrX_52942254_52963518 | FAM156A | chrX | 52942254 | 52963518 |
a0001c0001t0001g0079 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM156A_chrX_52942254_52963518 | FAM156A | chrX | 52942254 | 52963518 |
a0001c0001t0001g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM156A_chrX_52942254_52963518 | FAM156A | chrX | 52942254 | 52963518 |
a0001c0001t0001g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM156A_chrX_52942254_52963518 | FAM156A | chrX | 52942254 | 52963518 |
a0001c0001t0001g0086 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM156A_chrX_52942254_52963518 | FAM156A | chrX | 52942254 | 52963518 |
a0001c0001t0001g0087 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM156A_chrX_52942254_52963518 | FAM156A | chrX | 52942254 | 52963518 |
a0001c0001t0001g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM156A_chrX_52942254_52963518 | FAM156A | chrX | 52942254 | 52963518 |
a0001c0001t0002g0003 | 0/0 | 11 | 0 | 3 | 5 | 0 | 3 | FAM156A_chrX_52942254_52963518 | FAM156A | chrX | 52942254 | 52963518 |
a0001c0001t0002g0004 | 0/0 | 5 | 0 | 2 | 1 | 1 | 1 | FAM156A_chrX_52942254_52963518 | FAM156A | chrX | 52942254 | 52963518 |
a0001c0001t0002g0008 | 0/0 | 3 | 0 | 1 | 2 | 0 | 0 | FAM156A_chrX_52942254_52963518 | FAM156A | chrX | 52942254 | 52963518 |
a0001c0001t0002g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM156A_chrX_52942254_52963518 | FAM156A | chrX | 52942254 | 52963518 |
a0001c0001t0002g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM156A_chrX_52942254_52963518 | FAM156A | chrX | 52942254 | 52963518 |
a0001c0001t0002g0041 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM156A_chrX_52942254_52963518 | FAM156A | chrX | 52942254 | 52963518 |
a0001c0001t0002g0056 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM156A_chrX_52942254_52963518 | FAM156A | chrX | 52942254 | 52963518 |
a0001c0001t0002g0059 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM156A_chrX_52942254_52963518 | FAM156A | chrX | 52942254 | 52963518 |
a0001c0001t0002g0060 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM156A_chrX_52942254_52963518 | FAM156A | chrX | 52942254 | 52963518 |
a0001c0001t0002g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM156A_chrX_52942254_52963518 | FAM156A | chrX | 52942254 | 52963518 |
a0001c0001t0002g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM156A_chrX_52942254_52963518 | FAM156A | chrX | 52942254 | 52963518 |
a0001c0001t0002g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM156A_chrX_52942254_52963518 | FAM156A | chrX | 52942254 | 52963518 |
a0001c0001t0002g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM156A_chrX_52942254_52963518 | FAM156A | chrX | 52942254 | 52963518 |
a0001c0001t0002g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM156A_chrX_52942254_52963518 | FAM156A | chrX | 52942254 | 52963518 |
a0001c0001t0002g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM156A_chrX_52942254_52963518 | FAM156A | chrX | 52942254 | 52963518 |
a0001c0001t0002g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM156A_chrX_52942254_52963518 | FAM156A | chrX | 52942254 | 52963518 |
a0001c0001t0002g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM156A_chrX_52942254_52963518 | FAM156A | chrX | 52942254 | 52963518 |
a0001c0001t0002g0088 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM156A_chrX_52942254_52963518 | FAM156A | chrX | 52942254 | 52963518 |
a0001c0001t0003g0097 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM156A_chrX_52942254_52963518 | FAM156A | chrX | 52942254 | 52963518 |
a0001c0001t0003g0098 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM156A_chrX_52942254_52963518 | FAM156A | chrX | 52942254 | 52963518 |
a0001c0001t0003g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM156A_chrX_52942254_52963518 | FAM156A | chrX | 52942254 | 52963518 |
a0001c0001t0003g0100 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM156A_chrX_52942254_52963518 | FAM156A | chrX | 52942254 | 52963518 |
a0001c0001t0003g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM156A_chrX_52942254_52963518 | FAM156A | chrX | 52942254 | 52963518 |
a0001c0001t0003g0102 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM156A_chrX_52942254_52963518 | FAM156A | chrX | 52942254 | 52963518 |
a0001c0001t0003g0103 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM156A_chrX_52942254_52963518 | FAM156A | chrX | 52942254 | 52963518 |
a0001c0001t0003g0104 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM156A_chrX_52942254_52963518 | FAM156A | chrX | 52942254 | 52963518 |
a0001c0001t0003g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM156A_chrX_52942254_52963518 | FAM156A | chrX | 52942254 | 52963518 |
a0001c0001t0003g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM156A_chrX_52942254_52963518 | FAM156A | chrX | 52942254 | 52963518 |
a0001c0001t0004g0027 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM156A_chrX_52942254_52963518 | FAM156A | chrX | 52942254 | 52963518 |
a0001c0001t0004g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM156A_chrX_52942254_52963518 | FAM156A | chrX | 52942254 | 52963518 |
a0001c0001t0004g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM156A_chrX_52942254_52963518 | FAM156A | chrX | 52942254 | 52963518 |
a0001c0001t0004g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM156A_chrX_52942254_52963518 | FAM156A | chrX | 52942254 | 52963518 |
a0001c0001t0005g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM156A_chrX_52942254_52963518 | FAM156A | chrX | 52942254 | 52963518 |
a0001c0001t0005g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM156A_chrX_52942254_52963518 | FAM156A | chrX | 52942254 | 52963518 |
a0001c0001t0006g0018 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM156A_chrX_52942254_52963518 | FAM156A | chrX | 52942254 | 52963518 |
a0001c0001t0007g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM156A_chrX_52942254_52963518 | FAM156A | chrX | 52942254 | 52963518 |
a0001c0001t0008g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM156A_chrX_52942254_52963518 | FAM156A | chrX | 52942254 | 52963518 |
a0001c0001t0009g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM156A_chrX_52942254_52963518 | FAM156A | chrX | 52942254 | 52963518 |
a0001c0001t0010g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM156A_chrX_52942254_52963518 | FAM156A | chrX | 52942254 | 52963518 |
a0001c0001t0011g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM156A_chrX_52942254_52963518 | FAM156A | chrX | 52942254 | 52963518 |
a0001c0001t0012g0035 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM156A_chrX_52942254_52963518 | FAM156A | chrX | 52942254 | 52963518 |
a0001c0001t0013g0076 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM156A_chrX_52942254_52963518 | FAM156A | chrX | 52942254 | 52963518 |
a0001c0001t0015g0067 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM156A_chrX_52942254_52963518 | FAM156A | chrX | 52942254 | 52963518 |
a0001c0001t0016g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM156A_chrX_52942254_52963518 | FAM156A | chrX | 52942254 | 52963518 |
a0001c0001t0017g0030 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM156A_chrX_52942254_52963518 | FAM156A | chrX | 52942254 | 52963518 |
a0001c0001t0019g0090 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM156A_chrX_52942254_52963518 | FAM156A | chrX | 52942254 | 52963518 |
a0001c0001t0020g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM156A_chrX_52942254_52963518 | FAM156A | chrX | 52942254 | 52963518 |
a0001c0001t0021g0094 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM156A_chrX_52942254_52963518 | FAM156A | chrX | 52942254 | 52963518 |
a0001c0001t0022g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM156A_chrX_52942254_52963518 | FAM156A | chrX | 52942254 | 52963518 |
a0001c0001t0023g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM156A_chrX_52942254_52963518 | FAM156A | chrX | 52942254 | 52963518 |
a0002c0003t0002g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM156A_chrX_52942254_52963518 | FAM156A | chrX | 52942254 | 52963518 |
a0003c0004t0018g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM156A_chrX_52942254_52963518 | FAM156A | chrX | 52942254 | 52963518 |
a0004c0005t0002g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM156A_chrX_52942254_52963518 | FAM156A | chrX | 52942254 | 52963518 |
a0005c0006t0014g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM156A_chrX_52942254_52963518 | FAM156A | chrX | 52942254 | 52963518 |
a0006c0002t0001g0083 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM156A_chrX_52942254_52963518 | FAM156A | chrX | 52942254 | 52963518 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00280 | hp1 | a0001 | c0001 | t0003 | g0102 | EUR | FIN | FAM156A_chrX_52942254_52963518 | FAM156A | chrX | 52942254 | 52963518 |
HG00323 | hp1 | a0001 | c0001 | t0002 | g0060 | EUR | FIN | FAM156A_chrX_52942254_52963518 | FAM156A | chrX | 52942254 | 52963518 |
HG00323 | hp2 | a0001 | c0001 | t0002 | g0041 | EUR | FIN | FAM156A_chrX_52942254_52963518 | FAM156A | chrX | 52942254 | 52963518 |
HG00544 | hp1 | a0001 | c0001 | t0005 | g0092 | EAS | CHS | FAM156A_chrX_52942254_52963518 | FAM156A | chrX | 52942254 | 52963518 |
HG00544 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | CHS | FAM156A_chrX_52942254_52963518 | FAM156A | chrX | 52942254 | 52963518 |
HG00597 | hp1 | a0001 | c0001 | t0001 | g0007 | EAS | CHS | FAM156A_chrX_52942254_52963518 | FAM156A | chrX | 52942254 | 52963518 |
HG00597 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | FAM156A_chrX_52942254_52963518 | FAM156A | chrX | 52942254 | 52963518 |
HG00609 | hp1 | a0001 | c0001 | t0002 | g0003 | EAS | CHS | FAM156A_chrX_52942254_52963518 | FAM156A | chrX | 52942254 | 52963518 |
HG00621 | hp1 | a0001 | c0001 | t0007 | g0019 | EAS | CHS | FAM156A_chrX_52942254_52963518 | FAM156A | chrX | 52942254 | 52963518 |
HG00639 | hp1 | a0001 | c0001 | t0003 | g0101 | AMR | PUR | FAM156A_chrX_52942254_52963518 | FAM156A | chrX | 52942254 | 52963518 |
HG00639 | hp2 | a0001 | c0001 | t0006 | g0018 | AMR | PUR | FAM156A_chrX_52942254_52963518 | FAM156A | chrX | 52942254 | 52963518 |
HG00673 | hp1 | a0001 | c0001 | t0001 | g0033 | EAS | CHS | FAM156A_chrX_52942254_52963518 | FAM156A | chrX | 52942254 | 52963518 |
HG00735 | hp1 | a0001 | c0001 | t0001 | g0023 | AMR | PUR | FAM156A_chrX_52942254_52963518 | FAM156A | chrX | 52942254 | 52963518 |
HG00735 | hp2 | a0001 | c0001 | t0001 | g0075 | AMR | PUR | FAM156A_chrX_52942254_52963518 | FAM156A | chrX | 52942254 | 52963518 |
HG00738 | hp1 | a0001 | c0001 | t0001 | g0038 | AMR | PUR | FAM156A_chrX_52942254_52963518 | FAM156A | chrX | 52942254 | 52963518 |
HG00741 | hp1 | a0001 | c0001 | t0003 | g0098 | AMR | PUR | FAM156A_chrX_52942254_52963518 | FAM156A | chrX | 52942254 | 52963518 |
HG00741 | hp2 | a0001 | c0001 | t0002 | g0004 | AMR | PUR | FAM156A_chrX_52942254_52963518 | FAM156A | chrX | 52942254 | 52963518 |
HG01069 | hp1 | a0001 | c0001 | t0001 | g0031 | AMR | PUR | FAM156A_chrX_52942254_52963518 | FAM156A | chrX | 52942254 | 52963518 |
HG01071 | hp1 | a0001 | c0001 | t0001 | g0015 | AMR | PUR | FAM156A_chrX_52942254_52963518 | FAM156A | chrX | 52942254 | 52963518 |
HG01071 | hp2 | a0001 | c0001 | t0001 | g0049 | AMR | PUR | FAM156A_chrX_52942254_52963518 | FAM156A | chrX | 52942254 | 52963518 |
HG01074 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | FAM156A_chrX_52942254_52963518 | FAM156A | chrX | 52942254 | 52963518 |
HG01081 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | FAM156A_chrX_52942254_52963518 | FAM156A | chrX | 52942254 | 52963518 |
HG01081 | hp2 | a0001 | c0001 | t0001 | g0052 | AMR | PUR | FAM156A_chrX_52942254_52963518 | FAM156A | chrX | 52942254 | 52963518 |
HG01099 | hp1 | a0001 | c0001 | t0001 | g0005 | AMR | PUR | FAM156A_chrX_52942254_52963518 | FAM156A | chrX | 52942254 | 52963518 |
HG01106 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | FAM156A_chrX_52942254_52963518 | FAM156A | chrX | 52942254 | 52963518 |
HG01109 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | FAM156A_chrX_52942254_52963518 | FAM156A | chrX | 52942254 | 52963518 |
HG01167 | hp1 | a0001 | c0001 | t0002 | g0059 | AMR | PUR | FAM156A_chrX_52942254_52963518 | FAM156A | chrX | 52942254 | 52963518 |
HG01169 | hp1 | a0001 | c0001 | t0001 | g0087 | AMR | PUR | FAM156A_chrX_52942254_52963518 | FAM156A | chrX | 52942254 | 52963518 |
HG01169 | hp2 | a0001 | c0001 | t0002 | g0088 | AMR | PUR | FAM156A_chrX_52942254_52963518 | FAM156A | chrX | 52942254 | 52963518 |
HG01175 | hp1 | a0001 | c0001 | t0001 | g0053 | AMR | PUR | FAM156A_chrX_52942254_52963518 | FAM156A | chrX | 52942254 | 52963518 |
HG01175 | hp2 | a0001 | c0001 | t0001 | g0005 | AMR | PUR | FAM156A_chrX_52942254_52963518 | FAM156A | chrX | 52942254 | 52963518 |
HG01192 | hp1 | a0001 | c0001 | t0002 | g0004 | AMR | PUR | FAM156A_chrX_52942254_52963518 | FAM156A | chrX | 52942254 | 52963518 |
HG01243 | hp1 | a0001 | c0001 | t0001 | g0022 | AMR | PUR | FAM156A_chrX_52942254_52963518 | FAM156A | chrX | 52942254 | 52963518 |
HG01255 | hp1 | a0001 | c0001 | t0001 | g0034 | AMR | CLM | FAM156A_chrX_52942254_52963518 | FAM156A | chrX | 52942254 | 52963518 |
HG01256 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | CLM | FAM156A_chrX_52942254_52963518 | FAM156A | chrX | 52942254 | 52963518 |
HG01258 | hp1 | a0001 | c0001 | t0001 | g0005 | AMR | CLM | FAM156A_chrX_52942254_52963518 | FAM156A | chrX | 52942254 | 52963518 |
HG01261 | hp1 | a0001 | c0001 | t0002 | g0008 | AMR | CLM | FAM156A_chrX_52942254_52963518 | FAM156A | chrX | 52942254 | 52963518 |
HG01346 | hp1 | a0001 | c0001 | t0001 | g0070 | AMR | CLM | FAM156A_chrX_52942254_52963518 | FAM156A | chrX | 52942254 | 52963518 |
HG01346 | hp2 | a0001 | c0001 | t0003 | g0103 | AMR | CLM | FAM156A_chrX_52942254_52963518 | FAM156A | chrX | 52942254 | 52963518 |
HG01361 | hp1 | a0001 | c0001 | t0003 | g0104 | AMR | CLM | FAM156A_chrX_52942254_52963518 | FAM156A | chrX | 52942254 | 52963518 |
HG01361 | hp2 | a0001 | c0001 | t0001 | g0005 | AMR | CLM | FAM156A_chrX_52942254_52963518 | FAM156A | chrX | 52942254 | 52963518 |
HG01496 | hp1 | a0001 | c0001 | t0002 | g0003 | AMR | CLM | FAM156A_chrX_52942254_52963518 | FAM156A | chrX | 52942254 | 52963518 |
HG01496 | hp2 | a0001 | c0001 | t0002 | g0003 | AMR | CLM | FAM156A_chrX_52942254_52963518 | FAM156A | chrX | 52942254 | 52963518 |
HG01515 | hp1 | a0006 | c0002 | t0001 | g0083 | EUR | IBS | FAM156A_chrX_52942254_52963518 | FAM156A | chrX | 52942254 | 52963518 |
HG01884 | hp1 | a0001 | c0001 | t0001 | g0006 | AFR | ACB | FAM156A_chrX_52942254_52963518 | FAM156A | chrX | 52942254 | 52963518 |
HG01884 | hp2 | a0001 | c0001 | t0001 | g0037 | AFR | ACB | FAM156A_chrX_52942254_52963518 | FAM156A | chrX | 52942254 | 52963518 |
HG01928 | hp1 | a0001 | c0001 | t0001 | g0015 | AMR | PEL | FAM156A_chrX_52942254_52963518 | FAM156A | chrX | 52942254 | 52963518 |
HG01934 | hp1 | a0001 | c0001 | t0004 | g0027 | AMR | PEL | FAM156A_chrX_52942254_52963518 | FAM156A | chrX | 52942254 | 52963518 |
HG01981 | hp1 | a0001 | c0001 | t0015 | g0067 | AMR | PEL | FAM156A_chrX_52942254_52963518 | FAM156A | chrX | 52942254 | 52963518 |
HG01981 | hp2 | a0001 | c0001 | t0002 | g0003 | AMR | PEL | FAM156A_chrX_52942254_52963518 | FAM156A | chrX | 52942254 | 52963518 |
HG02004 | hp1 | a0001 | c0001 | t0001 | g0010 | AMR | PEL | FAM156A_chrX_52942254_52963518 | FAM156A | chrX | 52942254 | 52963518 |
HG02004 | hp2 | a0001 | c0001 | t0001 | g0007 | AMR | PEL | FAM156A_chrX_52942254_52963518 | FAM156A | chrX | 52942254 | 52963518 |
HG02015 | hp1 | a0001 | c0001 | t0002 | g0003 | EAS | KHV | FAM156A_chrX_52942254_52963518 | FAM156A | chrX | 52942254 | 52963518 |
HG02055 | hp1 | a0001 | c0001 | t0009 | g0021 | AFR | ACB | FAM156A_chrX_52942254_52963518 | FAM156A | chrX | 52942254 | 52963518 |
HG02074 | hp1 | a0001 | c0001 | t0023 | g0096 | EAS | KHV | FAM156A_chrX_52942254_52963518 | FAM156A | chrX | 52942254 | 52963518 |
HG02083 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | KHV | FAM156A_chrX_52942254_52963518 | FAM156A | chrX | 52942254 | 52963518 |
HG02132 | hp1 | a0001 | c0001 | t0001 | g0011 | EAS | KHV | FAM156A_chrX_52942254_52963518 | FAM156A | chrX | 52942254 | 52963518 |
HG02145 | hp1 | a0001 | c0001 | t0001 | g0073 | AFR | ACB | FAM156A_chrX_52942254_52963518 | FAM156A | chrX | 52942254 | 52963518 |
HG02258 | hp1 | a0001 | c0001 | t0001 | g0028 | AFR | ACB | FAM156A_chrX_52942254_52963518 | FAM156A | chrX | 52942254 | 52963518 |
HG02280 | hp1 | a0001 | c0001 | t0001 | g0051 | AFR | ACB | FAM156A_chrX_52942254_52963518 | FAM156A | chrX | 52942254 | 52963518 |
HG02280 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | ACB | FAM156A_chrX_52942254_52963518 | FAM156A | chrX | 52942254 | 52963518 |
HG02300 | hp1 | a0001 | c0001 | t0001 | g0084 | AMR | PEL | FAM156A_chrX_52942254_52963518 | FAM156A | chrX | 52942254 | 52963518 |
HG02602 | hp1 | a0001 | c0001 | t0002 | g0003 | SAS | PJL | FAM156A_chrX_52942254_52963518 | FAM156A | chrX | 52942254 | 52963518 |
HG02615 | hp1 | a0001 | c0001 | t0001 | g0007 | AFR | GWD | FAM156A_chrX_52942254_52963518 | FAM156A | chrX | 52942254 | 52963518 |
HG02615 | hp2 | a0001 | c0001 | t0001 | g0006 | AFR | GWD | FAM156A_chrX_52942254_52963518 | FAM156A | chrX | 52942254 | 52963518 |
HG02647 | hp1 | a0003 | c0004 | t0018 | g0066 | AFR | GWD | FAM156A_chrX_52942254_52963518 | FAM156A | chrX | 52942254 | 52963518 |
HG02698 | hp1 | a0001 | c0001 | t0002 | g0004 | SAS | PJL | FAM156A_chrX_52942254_52963518 | FAM156A | chrX | 52942254 | 52963518 |
HG02735 | hp1 | a0001 | c0001 | t0001 | g0010 | SAS | PJL | FAM156A_chrX_52942254_52963518 | FAM156A | chrX | 52942254 | 52963518 |
HG02738 | hp1 | a0001 | c0001 | t0002 | g0056 | SAS | PJL | FAM156A_chrX_52942254_52963518 | FAM156A | chrX | 52942254 | 52963518 |
HG02809 | hp1 | a0001 | c0001 | t0001 | g0012 | AFR | GWD | FAM156A_chrX_52942254_52963518 | FAM156A | chrX | 52942254 | 52963518 |
HG02809 | hp2 | a0001 | c0001 | t0001 | g0013 | AFR | GWD | FAM156A_chrX_52942254_52963518 | FAM156A | chrX | 52942254 | 52963518 |
HG02818 | hp1 | a0001 | c0001 | t0001 | g0007 | AFR | GWD | FAM156A_chrX_52942254_52963518 | FAM156A | chrX | 52942254 | 52963518 |
HG02818 | hp2 | a0001 | c0001 | t0004 | g0054 | AFR | GWD | FAM156A_chrX_52942254_52963518 | FAM156A | chrX | 52942254 | 52963518 |
HG02886 | hp1 | a0001 | c0001 | t0001 | g0039 | AFR | GWD | FAM156A_chrX_52942254_52963518 | FAM156A | chrX | 52942254 | 52963518 |
HG02886 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | GWD | FAM156A_chrX_52942254_52963518 | FAM156A | chrX | 52942254 | 52963518 |
HG02965 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | ESN | FAM156A_chrX_52942254_52963518 | FAM156A | chrX | 52942254 | 52963518 |
HG02970 | hp1 | a0001 | c0001 | t0001 | g0078 | AFR | ESN | FAM156A_chrX_52942254_52963518 | FAM156A | chrX | 52942254 | 52963518 |
HG02970 | hp2 | a0001 | c0001 | t0001 | g0014 | AFR | ESN | FAM156A_chrX_52942254_52963518 | FAM156A | chrX | 52942254 | 52963518 |
HG03041 | hp1 | a0001 | c0001 | t0001 | g0013 | AFR | GWD | FAM156A_chrX_52942254_52963518 | FAM156A | chrX | 52942254 | 52963518 |
HG03041 | hp2 | a0001 | c0001 | t0001 | g0017 | AFR | GWD | FAM156A_chrX_52942254_52963518 | FAM156A | chrX | 52942254 | 52963518 |
HG03098 | hp1 | a0001 | c0001 | t0002 | g0029 | AFR | MSL | FAM156A_chrX_52942254_52963518 | FAM156A | chrX | 52942254 | 52963518 |
HG03130 | hp1 | a0001 | c0001 | t0002 | g0068 | AFR | ESN | FAM156A_chrX_52942254_52963518 | FAM156A | chrX | 52942254 | 52963518 |
HG03139 | hp1 | a0001 | c0001 | t0004 | g0081 | AFR | ESN | FAM156A_chrX_52942254_52963518 | FAM156A | chrX | 52942254 | 52963518 |
HG03195 | hp1 | a0001 | c0001 | t0001 | g0009 | AFR | ESN | FAM156A_chrX_52942254_52963518 | FAM156A | chrX | 52942254 | 52963518 |
HG03195 | hp2 | a0001 | c0001 | t0003 | g0099 | AFR | ESN | FAM156A_chrX_52942254_52963518 | FAM156A | chrX | 52942254 | 52963518 |
HG03209 | hp1 | a0001 | c0001 | t0001 | g0006 | AFR | MSL | FAM156A_chrX_52942254_52963518 | FAM156A | chrX | 52942254 | 52963518 |
HG03453 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | MSL | FAM156A_chrX_52942254_52963518 | FAM156A | chrX | 52942254 | 52963518 |
HG03453 | hp2 | a0001 | c0001 | t0003 | g0105 | AFR | MSL | FAM156A_chrX_52942254_52963518 | FAM156A | chrX | 52942254 | 52963518 |
HG03486 | hp1 | a0001 | c0001 | t0004 | g0082 | AFR | MSL | FAM156A_chrX_52942254_52963518 | FAM156A | chrX | 52942254 | 52963518 |
HG03486 | hp2 | a0001 | c0001 | t0001 | g0006 | AFR | MSL | FAM156A_chrX_52942254_52963518 | FAM156A | chrX | 52942254 | 52963518 |
HG03490 | hp1 | a0001 | c0001 | t0002 | g0003 | SAS | PJL | FAM156A_chrX_52942254_52963518 | FAM156A | chrX | 52942254 | 52963518 |
HG03492 | hp1 | a0001 | c0001 | t0017 | g0030 | SAS | PJL | FAM156A_chrX_52942254_52963518 | FAM156A | chrX | 52942254 | 52963518 |
HG03516 | hp1 | a0001 | c0001 | t0011 | g0058 | AFR | ESN | FAM156A_chrX_52942254_52963518 | FAM156A | chrX | 52942254 | 52963518 |
HG03516 | hp2 | a0002 | c0003 | t0002 | g0061 | AFR | ESN | FAM156A_chrX_52942254_52963518 | FAM156A | chrX | 52942254 | 52963518 |
HG03540 | hp1 | a0001 | c0001 | t0001 | g0009 | AFR | GWD | FAM156A_chrX_52942254_52963518 | FAM156A | chrX | 52942254 | 52963518 |
HG03540 | hp2 | a0001 | c0001 | t0001 | g0016 | AFR | GWD | FAM156A_chrX_52942254_52963518 | FAM156A | chrX | 52942254 | 52963518 |
HG03579 | hp1 | a0001 | c0001 | t0010 | g0055 | AFR | MSL | FAM156A_chrX_52942254_52963518 | FAM156A | chrX | 52942254 | 52963518 |
HG03654 | hp1 | a0001 | c0001 | t0012 | g0035 | SAS | PJL | FAM156A_chrX_52942254_52963518 | FAM156A | chrX | 52942254 | 52963518 |
HG03669 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | FAM156A_chrX_52942254_52963518 | FAM156A | chrX | 52942254 | 52963518 |
HG03669 | hp2 | a0001 | c0001 | t0001 | g0002 | SAS | PJL | FAM156A_chrX_52942254_52963518 | FAM156A | chrX | 52942254 | 52963518 |
HG03688 | hp1 | a0001 | c0001 | t0021 | g0094 | SAS | STU | FAM156A_chrX_52942254_52963518 | FAM156A | chrX | 52942254 | 52963518 |
HG03704 | hp1 | a0001 | c0001 | t0001 | g0079 | SAS | PJL | FAM156A_chrX_52942254_52963518 | FAM156A | chrX | 52942254 | 52963518 |
HG03704 | hp2 | a0001 | c0001 | t0001 | g0086 | SAS | PJL | FAM156A_chrX_52942254_52963518 | FAM156A | chrX | 52942254 | 52963518 |
HG03710 | hp1 | a0001 | c0001 | t0001 | g0002 | SAS | PJL | FAM156A_chrX_52942254_52963518 | FAM156A | chrX | 52942254 | 52963518 |
HG03942 | hp1 | a0001 | c0001 | t0001 | g0057 | SAS | BEB | FAM156A_chrX_52942254_52963518 | FAM156A | chrX | 52942254 | 52963518 |
HG04115 | hp1 | a0001 | c0001 | t0002 | g0003 | SAS | STU | FAM156A_chrX_52942254_52963518 | FAM156A | chrX | 52942254 | 52963518 |
HG04199 | hp1 | a0001 | c0001 | t0013 | g0076 | SAS | STU | FAM156A_chrX_52942254_52963518 | FAM156A | chrX | 52942254 | 52963518 |
HG04204 | hp1 | a0001 | c0001 | t0001 | g0032 | SAS | STU | FAM156A_chrX_52942254_52963518 | FAM156A | chrX | 52942254 | 52963518 |
HG04228 | hp1 | a0001 | c0001 | t0003 | g0097 | SAS | STU | FAM156A_chrX_52942254_52963518 | FAM156A | chrX | 52942254 | 52963518 |
NA18522 | hp1 | a0001 | c0001 | t0022 | g0095 | AFR | YRI | FAM156A_chrX_52942254_52963518 | FAM156A | chrX | 52942254 | 52963518 |
NA18612 | hp1 | a0001 | c0001 | t0020 | g0091 | EAS | CHB | FAM156A_chrX_52942254_52963518 | FAM156A | chrX | 52942254 | 52963518 |
NA18906 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | YRI | FAM156A_chrX_52942254_52963518 | FAM156A | chrX | 52942254 | 52963518 |
NA18906 | hp2 | a0001 | c0001 | t0001 | g0016 | AFR | YRI | FAM156A_chrX_52942254_52963518 | FAM156A | chrX | 52942254 | 52963518 |
NA18944 | hp1 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | FAM156A_chrX_52942254_52963518 | FAM156A | chrX | 52942254 | 52963518 |
NA18948 | hp1 | a0001 | c0001 | t0001 | g0046 | EAS | JPT | FAM156A_chrX_52942254_52963518 | FAM156A | chrX | 52942254 | 52963518 |
NA18950 | hp1 | a0001 | c0001 | t0001 | g0040 | EAS | JPT | FAM156A_chrX_52942254_52963518 | FAM156A | chrX | 52942254 | 52963518 |
NA18950 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | FAM156A_chrX_52942254_52963518 | FAM156A | chrX | 52942254 | 52963518 |
NA18952 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | FAM156A_chrX_52942254_52963518 | FAM156A | chrX | 52942254 | 52963518 |
NA18957 | hp1 | a0001 | c0001 | t0016 | g0069 | EAS | JPT | FAM156A_chrX_52942254_52963518 | FAM156A | chrX | 52942254 | 52963518 |
NA18957 | hp2 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | FAM156A_chrX_52942254_52963518 | FAM156A | chrX | 52942254 | 52963518 |
NA18960 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | FAM156A_chrX_52942254_52963518 | FAM156A | chrX | 52942254 | 52963518 |
NA18966 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | FAM156A_chrX_52942254_52963518 | FAM156A | chrX | 52942254 | 52963518 |
NA18967 | hp1 | a0001 | c0001 | t0002 | g0074 | EAS | JPT | FAM156A_chrX_52942254_52963518 | FAM156A | chrX | 52942254 | 52963518 |
NA18968 | hp1 | a0001 | c0001 | t0002 | g0008 | EAS | JPT | FAM156A_chrX_52942254_52963518 | FAM156A | chrX | 52942254 | 52963518 |
NA18968 | hp2 | a0001 | c0001 | t0001 | g0050 | EAS | JPT | FAM156A_chrX_52942254_52963518 | FAM156A | chrX | 52942254 | 52963518 |
NA18969 | hp1 | a0001 | c0001 | t0002 | g0063 | EAS | JPT | FAM156A_chrX_52942254_52963518 | FAM156A | chrX | 52942254 | 52963518 |
NA18969 | hp2 | a0001 | c0001 | t0002 | g0065 | EAS | JPT | FAM156A_chrX_52942254_52963518 | FAM156A | chrX | 52942254 | 52963518 |
NA18970 | hp1 | a0001 | c0001 | t0002 | g0036 | EAS | JPT | FAM156A_chrX_52942254_52963518 | FAM156A | chrX | 52942254 | 52963518 |
NA18971 | hp1 | a0001 | c0001 | t0001 | g0017 | EAS | JPT | FAM156A_chrX_52942254_52963518 | FAM156A | chrX | 52942254 | 52963518 |
NA18974 | hp1 | a0001 | c0001 | t0002 | g0085 | EAS | JPT | FAM156A_chrX_52942254_52963518 | FAM156A | chrX | 52942254 | 52963518 |
NA18977 | hp1 | a0005 | c0006 | t0014 | g0048 | EAS | JPT | FAM156A_chrX_52942254_52963518 | FAM156A | chrX | 52942254 | 52963518 |
NA18979 | hp1 | a0001 | c0001 | t0002 | g0008 | EAS | JPT | FAM156A_chrX_52942254_52963518 | FAM156A | chrX | 52942254 | 52963518 |
NA18979 | hp2 | a0001 | c0001 | t0001 | g0047 | EAS | JPT | FAM156A_chrX_52942254_52963518 | FAM156A | chrX | 52942254 | 52963518 |
NA18982 | hp1 | a0001 | c0001 | t0001 | g0077 | EAS | JPT | FAM156A_chrX_52942254_52963518 | FAM156A | chrX | 52942254 | 52963518 |
NA18983 | hp1 | a0001 | c0001 | t0002 | g0004 | EAS | JPT | FAM156A_chrX_52942254_52963518 | FAM156A | chrX | 52942254 | 52963518 |
NA18984 | hp1 | a0001 | c0001 | t0001 | g0062 | EAS | JPT | FAM156A_chrX_52942254_52963518 | FAM156A | chrX | 52942254 | 52963518 |
NA18986 | hp1 | a0001 | c0001 | t0002 | g0072 | EAS | JPT | FAM156A_chrX_52942254_52963518 | FAM156A | chrX | 52942254 | 52963518 |
NA18989 | hp1 | a0001 | c0001 | t0001 | g0025 | EAS | JPT | FAM156A_chrX_52942254_52963518 | FAM156A | chrX | 52942254 | 52963518 |
NA18990 | hp1 | a0001 | c0001 | t0002 | g0064 | EAS | JPT | FAM156A_chrX_52942254_52963518 | FAM156A | chrX | 52942254 | 52963518 |
NA19004 | hp1 | a0001 | c0001 | t0001 | g0044 | EAS | JPT | FAM156A_chrX_52942254_52963518 | FAM156A | chrX | 52942254 | 52963518 |
NA19007 | hp1 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | FAM156A_chrX_52942254_52963518 | FAM156A | chrX | 52942254 | 52963518 |
NA19011 | hp1 | a0001 | c0001 | t0001 | g0080 | EAS | JPT | FAM156A_chrX_52942254_52963518 | FAM156A | chrX | 52942254 | 52963518 |
NA19011 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | FAM156A_chrX_52942254_52963518 | FAM156A | chrX | 52942254 | 52963518 |
NA19012 | hp1 | a0001 | c0001 | t0002 | g0071 | EAS | JPT | FAM156A_chrX_52942254_52963518 | FAM156A | chrX | 52942254 | 52963518 |
NA19030 | hp1 | a0001 | c0001 | t0001 | g0026 | AFR | LWK | FAM156A_chrX_52942254_52963518 | FAM156A | chrX | 52942254 | 52963518 |
NA19030 | hp2 | a0001 | c0001 | t0001 | g0043 | AFR | LWK | FAM156A_chrX_52942254_52963518 | FAM156A | chrX | 52942254 | 52963518 |
NA19043 | hp1 | a0001 | c0001 | t0008 | g0020 | AFR | LWK | FAM156A_chrX_52942254_52963518 | FAM156A | chrX | 52942254 | 52963518 |
NA19060 | hp1 | a0004 | c0005 | t0002 | g0045 | EAS | JPT | FAM156A_chrX_52942254_52963518 | FAM156A | chrX | 52942254 | 52963518 |
NA19062 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | FAM156A_chrX_52942254_52963518 | FAM156A | chrX | 52942254 | 52963518 |
NA19063 | hp1 | a0001 | c0001 | t0001 | g0042 | EAS | JPT | FAM156A_chrX_52942254_52963518 | FAM156A | chrX | 52942254 | 52963518 |
NA19066 | hp1 | a0001 | c0001 | t0005 | g0093 | EAS | JPT | FAM156A_chrX_52942254_52963518 | FAM156A | chrX | 52942254 | 52963518 |
NA19085 | hp1 | a0001 | c0001 | t0001 | g0089 | EAS | JPT | FAM156A_chrX_52942254_52963518 | FAM156A | chrX | 52942254 | 52963518 |
NA19089 | hp1 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | FAM156A_chrX_52942254_52963518 | FAM156A | chrX | 52942254 | 52963518 |
NA19091 | hp1 | a0001 | c0001 | t0001 | g0024 | EAS | JPT | FAM156A_chrX_52942254_52963518 | FAM156A | chrX | 52942254 | 52963518 |
NA20752 | hp1 | a0001 | c0001 | t0002 | g0004 | EUR | TSI | FAM156A_chrX_52942254_52963518 | FAM156A | chrX | 52942254 | 52963518 |
NA20805 | hp1 | a0001 | c0001 | t0003 | g0100 | EUR | TSI | FAM156A_chrX_52942254_52963518 | FAM156A | chrX | 52942254 | 52963518 |
NA20905 | hp1 | a0001 | c0001 | t0019 | g0090 | SAS | GIH | FAM156A_chrX_52942254_52963518 | FAM156A | chrX | 52942254 | 52963518 |
HG02486 | hp1 | a0001 | c0001 | t0001 | g0014 | AFR | ACB | FAM156A_chrX_52942254_52963518 | FAM156A | chrX | 52942254 | 52963518 |
HG03471 | hp1 | a0001 | c0001 | t0003 | g0106 | AFR | MSL | FAM156A_chrX_52942254_52963518 | FAM156A | chrX | 52942254 | 52963518 |
HG06807 | hp1 | a0001 | c0001 | t0001 | g0012 | AFR | USA | FAM156A_chrX_52942254_52963518 | FAM156A | chrX | 52942254 | 52963518 |
HG06807 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | USA | FAM156A_chrX_52942254_52963518 | FAM156A | chrX | 52942254 | 52963518 |
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:52947976
|
G | GC | 1 | a0006 | 1 | HG01515.hp1 | frameshift_variant | HIGH | c.612dupG | p.Leu205fs | FAM156A | ENSG00000268350.8 | transcript | ENST00000622447.5 | protein_coding | 3/3 | 3068/3791 | 612/642 | 204/213 | chrX | 52947976 | ||
chrX:52948109
|
G | GC | 1 | a0005 | 1 | NA18977.hp1 | frameshift_variant | HIGH | c.479dupG | p.Leu161fs | FAM156A | ENSG00000268350.8 | transcript | ENST00000622447.5 | protein_coding | 3/3 | 2935/3791 | 479/642 | 160/213 | chrX | 52948109 | ||
chrX:52948296
|
T | TG | 1 | a0003 | 1 | HG02647.hp1 | frameshift_variant | HIGH | c.292dupC | p.His98fs | FAM156A | ENSG00000268350.8 | transcript | ENST00000622447.5 | protein_coding | 3/3 | 2748/3791 | 292/642 | 98/213 | chrX | 52948296 | ||
chrX:52948328
|
C | CT | 1 | a0004 | 1 | NA19060.hp1 | frameshift_variant | HIGH | c.260dupA | p.Lys88fs | FAM156A | ENSG00000268350.8 | transcript | ENST00000622447.5 | protein_coding | 3/3 | 2716/3791 | 260/642 | 87/213 | chrX | 52948328 | ||
chrX:52948392
|
C | T | 2 | a0002a0003 | 2 | HG02647.hp1 HG03516.hp2 |
missense_variant | MODERATE | c.197G>A | p.Arg66Gln | FAM156A | ENSG00000268350.8 | transcript | ENST00000622447.5 | protein_coding | 3/3 | 2653/3791 | 197/642 | 66/213 | chrX | 52948392 | ||
chrX:52948515
|
TG | T | 1 | a0006 | 1 | HG01515.hp1 | frameshift_variant | HIGH | c.73delC | p.Gln25fs | FAM156A | ENSG00000268350.8 | transcript | ENST00000622447.5 | protein_coding | 3/3 | 2529/3791 | 73/642 | 25/213 | chrX | 52948515 |
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:52947290
|
A | ATG | 1 | a0001c0001t0015 | 1 | HG01981.hp1 | 3_prime_UTR_variant | MODIFIER | c.*655_*656dupCA | FAM156A | ENSG00000268350.8 | transcript | ENST00000622447.5 | protein_coding | 3/3 | 656 | chrX | 52947290 | |||||
chrX:52947297
|
A | AC | 1 | a0005c0006t0014 | 1 | NA18977.hp1 | 3_prime_UTR_variant | MODIFIER | c.*649dupG | FAM156A | ENSG00000268350.8 | transcript | ENST00000622447.5 | protein_coding | 3/3 | 649 | chrX | 52947297 | |||||
chrX:52947297
|
AC | A | 1 | a0001c0001t0012 | 1 | HG03654.hp1 | 3_prime_UTR_variant | MODIFIER | c.*649delG | FAM156A | ENSG00000268350.8 | transcript | ENST00000622447.5 | protein_coding | 3/3 | 649 | chrX | 52947297 | |||||
chrX:52947507
|
AG | A | 1 | a0001c0001t0020 | 1 | NA18612.hp1 | 3_prime_UTR_variant | MODIFIER | c.*439delC | FAM156A | ENSG00000268350.8 | transcript | ENST00000622447.5 | protein_coding | 3/3 | 439 | chrX | 52947507 | |||||
chrX:52947574
|
T | C | 1 | a0001c0001t0016 | 1 | NA18957.hp1 | 3_prime_UTR_variant | MODIFIER | c.*373A>G | FAM156A | ENSG00000268350.8 | transcript | ENST00000622447.5 | protein_coding | 3/3 | 373 | chrX | 52947574 | |||||
chrX:52947664
|
AG | A | 1 | a0001c0001t0012 | 1 | HG03654.hp1 | 3_prime_UTR_variant | MODIFIER | c.*282delC | FAM156A | ENSG00000268350.8 | transcript | ENST00000622447.5 | protein_coding | 3/3 | 282 | chrX | 52947664 | |||||
chrX:52947700
|
G | A | 1 | a0001c0001t0013 | 1 | HG04199.hp1 | 3_prime_UTR_variant | MODIFIER | c.*247C>T | FAM156A | ENSG00000268350.8 | transcript | ENST00000622447.5 | protein_coding | 3/3 | 247 | chrX | 52947700 | |||||
chrX:52947705
|
G | A | 11 | a0001c0001t0002a0001c0001t0005a0001c0001t0008others(8): Show | 45 | HG00323.hp1 HG00323.hp2 HG00544.hp1 others(42): Show |
3_prime_UTR_variant | MODIFIER | c.*242C>T | FAM156A | ENSG00000268350.8 | transcript | ENST00000622447.5 | protein_coding | 3/3 | 242 | chrX | 52947705 | |||||
chrX:52947806
|
C | G | 1 | a0001c0001t0011 | 1 | HG03516.hp1 | 3_prime_UTR_variant | MODIFIER | c.*141G>C | FAM156A | ENSG00000268350.8 | transcript | ENST00000622447.5 | protein_coding | 3/3 | 141 | chrX | 52947806 | |||||
chrX:52947814
|
G | A | 1 | a0001c0001t0017 | 1 | HG03492.hp1 | 3_prime_UTR_variant | MODIFIER | c.*133C>T | FAM156A | ENSG00000268350.8 | transcript | ENST00000622447.5 | protein_coding | 3/3 | 133 | chrX | 52947814 | |||||
chrX:52947836
|
T | TC | 1 | a0003c0004t0018 | 1 | HG02647.hp1 | 3_prime_UTR_variant | MODIFIER | c.*110dupG | FAM156A | ENSG00000268350.8 | transcript | ENST00000622447.5 | protein_coding | 3/3 | 110 | chrX | 52947836 | |||||
chrX:52955193
|
A | G | 1 | a0001c0001t0010 | 1 | HG03579.hp1 | 5_prime_UTR_variant | MODIFIER | c.-157T>C | FAM156A | ENSG00000268350.8 | transcript | ENST00000622447.5 | protein_coding | 2/3 | 6605 | chrX | 52955193 | |||||
chrX:52955207
|
G | A | 1 | a0001c0001t0004 | 4 | HG01934.hp1 HG02818.hp2 HG03139.hp1 others(1): Show |
5_prime_UTR_variant | MODIFIER | c.-171C>T | FAM156A | ENSG00000268350.8 | transcript | ENST00000622447.5 | protein_coding | 2/3 | 6619 | chrX | 52955207 | |||||
chrX:52955220
|
T | TC | 1 | a0001c0001t0023 | 1 | HG02074.hp1 | 5_prime_UTR_variant | MODIFIER | c.-185dupG | FAM156A | ENSG00000268350.8 | transcript | ENST00000622447.5 | protein_coding | 2/3 | 6633 | chrX | 52955220 | |||||
chrX:52956365
|
T | TC | 1 | a0001c0001t0006 | 1 | HG00639.hp2 | 5_prime_UTR_variant | MODIFIER | c.-304dupG | FAM156A | ENSG00000268350.8 | transcript | ENST00000622447.5 | protein_coding | 1/3 | 7778 | chrX | 52956365 | |||||
chrX:52956478
|
GA | G | 1 | a0001c0001t0006 | 1 | HG00639.hp2 | 5_prime_UTR_variant | MODIFIER | c.-417delT | FAM156A | ENSG00000268350.8 | transcript | ENST00000622447.5 | protein_coding | 1/3 | 7891 | chrX | 52956478 | |||||
chrX:52956712
|
GT | G | 1 | a0001c0001t0006 | 1 | HG00639.hp2 | 5_prime_UTR_variant | MODIFIER | c.-651delA | FAM156A | ENSG00000268350.8 | transcript | ENST00000622447.5 | protein_coding | 1/3 | 8125 | chrX | 52956712 | |||||
chrX:52956765
|
CA | C | 1 | a0001c0001t0022 | 1 | NA18522.hp1 | 5_prime_UTR_variant | MODIFIER | c.-704delT | FAM156A | ENSG00000268350.8 | transcript | ENST00000622447.5 | protein_coding | 1/3 | 8178 | chrX | 52956765 | |||||
chrX:52956803
|
C | CG | 1 | a0001c0001t0009 | 1 | HG02055.hp1 | 5_prime_UTR_variant | MODIFIER | c.-742dupC | FAM156A | ENSG00000268350.8 | transcript | ENST00000622447.5 | protein_coding | 1/3 | 8216 | chrX | 52956803 | |||||
chrX:52956897
|
TC | T | 1 | a0001c0001t0008 | 1 | NA19043.hp1 | 5_prime_UTR_variant | MODIFIER | c.-836delG | FAM156A | ENSG00000268350.8 | transcript | ENST00000622447.5 | protein_coding | 1/3 | 8310 | chrX | 52956897 | |||||
chrX:52957369
|
C | CT | 1 | a0001c0001t0006 | 1 | HG00639.hp2 | 5_prime_UTR_variant | MODIFIER | c.-1308dupA | FAM156A | ENSG00000268350.8 | transcript | ENST00000622447.5 | protein_coding | 1/3 | 8782 | chrX | 52957369 | |||||
chrX:52957391
|
A | AG | 1 | a0001c0001t0006 | 1 | HG00639.hp2 | 5_prime_UTR_variant | MODIFIER | c.-1330dupC | FAM156A | ENSG00000268350.8 | transcript | ENST00000622447.5 | protein_coding | 1/3 | 8804 | chrX | 52957391 | |||||
chrX:52957540
|
C | CT | 1 | a0001c0001t0006 | 1 | HG00639.hp2 | 5_prime_UTR_variant | MODIFIER | c.-1479dupA | FAM156A | ENSG00000268350.8 | transcript | ENST00000622447.5 | protein_coding | 1/3 | 8953 | chrX | 52957540 | |||||
chrX:52957563
|
A | AC | 1 | a0001c0001t0006 | 1 | HG00639.hp2 | 5_prime_UTR_variant | MODIFIER | c.-1502dupG | FAM156A | ENSG00000268350.8 | transcript | ENST00000622447.5 | protein_coding | 1/3 | 8976 | chrX | 52957563 | |||||
chrX:52957742
|
G | GC | 1 | a0001c0001t0006 | 1 | HG00639.hp2 | 5_prime_UTR_variant | MODIFIER | c.-1681dupG | FAM156A | ENSG00000268350.8 | transcript | ENST00000622447.5 | protein_coding | 1/3 | 9155 | chrX | 52957742 | |||||
chrX:52957844
|
T | TA | 1 | a0001c0001t0019 | 1 | NA20905.hp1 | 5_prime_UTR_variant | MODIFIER | c.-1783dupT | FAM156A | ENSG00000268350.8 | transcript | ENST00000622447.5 | protein_coding | 1/3 | 9257 | chrX | 52957844 | |||||
chrX:52957917
|
GGTTT | G | 2 | a0001c0001t0005a0001c0001t0020 | 3 | HG00544.hp1 NA18612.hp1 NA19066.hp1 |
5_prime_UTR_variant | MODIFIER | c.-1859_-1856delAAAC | FAM156A | ENSG00000268350.8 | transcript | ENST00000622447.5 | protein_coding | 1/3 | 9330 | chrX | 52957917 | |||||
chrX:52957959
|
TC | T | 1 | a0001c0001t0006 | 1 | HG00639.hp2 | 5_prime_UTR_variant | MODIFIER | c.-1898delG | FAM156A | ENSG00000268350.8 | transcript | ENST00000622447.5 | protein_coding | 1/3 | 9372 | chrX | 52957959 | |||||
chrX:52957985
|
T | TG | 1 | a0001c0001t0006 | 1 | HG00639.hp2 | 5_prime_UTR_variant | MODIFIER | c.-1924dupC | FAM156A | ENSG00000268350.8 | transcript | ENST00000622447.5 | protein_coding | 1/3 | 9398 | chrX | 52957985 | |||||
chrX:52958054
|
C | CA | 1 | a0001c0001t0006 | 1 | HG00639.hp2 | 5_prime_UTR_variant | MODIFIER | c.-1993_-1992insT | FAM156A | ENSG00000268350.8 | transcript | ENST00000622447.5 | protein_coding | 1/3 | 9467 | chrX | 52958054 | |||||
chrX:52958223
|
G | GA | 1 | a0001c0001t0006 | 1 | HG00639.hp2 | 5_prime_UTR_variant | MODIFIER | c.-2162dupT | FAM156A | ENSG00000268350.8 | transcript | ENST00000622447.5 | protein_coding | 1/3 | 9636 | chrX | 52958223 | |||||
chrX:52958228
|
C | CA | 1 | a0001c0001t0006 | 1 | HG00639.hp2 | 5_prime_UTR_variant | MODIFIER | c.-2167_-2166insT | FAM156A | ENSG00000268350.8 | transcript | ENST00000622447.5 | protein_coding | 1/3 | 9641 | chrX | 52958228 | |||||
chrX:52958243
|
G | GC | 1 | a0001c0001t0006 | 1 | HG00639.hp2 | 5_prime_UTR_variant | MODIFIER | c.-2182dupG | FAM156A | ENSG00000268350.8 | transcript | ENST00000622447.5 | protein_coding | 1/3 | 9656 | chrX | 52958243 | |||||
chrX:52958331
|
T | A | 1 | a0001c0001t0021 | 1 | HG03688.hp1 | 5_prime_UTR_variant | MODIFIER | c.-2269A>T | FAM156A | ENSG00000268350.8 | transcript | ENST00000622447.5 | protein_coding | 1/3 | 9743 | chrX | 52958331 | |||||
chrX:52958341
|
AC | A | 3 | a0001c0001t0003a0001c0001t0022a0001c0001t0023 | 12 | HG00280.hp1 HG00639.hp1 HG00741.hp1 others(9): Show |
5_prime_UTR_variant | MODIFIER | c.-2280delG | FAM156A | ENSG00000268350.8 | transcript | ENST00000622447.5 | protein_coding | 1/3 | 9754 | chrX | 52958341 | |||||
chrX:52958390
|
C | T | 1 | a0001c0001t0007 | 1 | HG00621.hp1 | 5_prime_UTR_variant | MODIFIER | c.-2328G>A | FAM156A | ENSG00000268350.8 | transcript | ENST00000622447.5 | protein_coding | 1/3 | 9802 | chrX | 52958390 | |||||
chrX:52958498
|
A | T | 1 | a0001c0001t0006 | 1 | HG00639.hp2 | 5_prime_UTR_variant | MODIFIER | c.-2436T>A | FAM156A | ENSG00000268350.8 | transcript | ENST00000622447.5 | protein_coding | 1/3 | 9910 | chrX | 52958498 |
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:52948868
|
T | A | 1 | a0006c0002t0001g0083 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.-117-163A>T | FAM156A | ENSG00000268350.8 | transcript | ENST00000622447.5 | protein_coding | 2/2 | chrX | 52948868 | ||||||
chrX:52948925
|
CG | C | 1 | a0004c0005t0002g0045 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.-117-221delC | FAM156A | ENSG00000268350.8 | transcript | ENST00000622447.5 | protein_coding | 2/2 | chrX | 52948925 | ||||||
chrX:52948967
|
C | T | 11 | a0001c0001t0003g0097a0001c0001t0003g0098a0001c0001t0003g0099others(8): Show | 11 | HG00280.hp1 HG00639.hp1 HG00741.hp1 others(8): Show |
intron_variant | MODIFIER | c.-117-262G>A | FAM156A | ENSG00000268350.8 | transcript | ENST00000622447.5 | protein_coding | 2/2 | chrX | 52948967 | ||||||
chrX:52948976
|
AT | A | 1 | a0006c0002t0001g0083 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.-117-272delA | FAM156A | ENSG00000268350.8 | transcript | ENST00000622447.5 | protein_coding | 2/2 | chrX | 52948976 | ||||||
chrX:52949096
|
GT | G | 1 | a0006c0002t0001g0083 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.-117-392delA | FAM156A | ENSG00000268350.8 | transcript | ENST00000622447.5 | protein_coding | 2/2 | chrX | 52949096 | ||||||
chrX:52949106
|
T | TG | 1 | a0001c0001t0001g0077 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.-117-402dupC | FAM156A | ENSG00000268350.8 | transcript | ENST00000622447.5 | protein_coding | 2/2 | chrX | 52949106 | ||||||
chrX:52949106
|
TG | T | 1 | a0001c0001t0002g0056 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.-117-402delC | FAM156A | ENSG00000268350.8 | transcript | ENST00000622447.5 | protein_coding | 2/2 | chrX | 52949106 | ||||||
chrX:52949140
|
A | AC | 1 | a0006c0002t0001g0083 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.-117-436dupG | FAM156A | ENSG00000268350.8 | transcript | ENST00000622447.5 | protein_coding | 2/2 | chrX | 52949140 | ||||||
chrX:52949179
|
C | T | 2 | a0002c0003t0002g0061a0003c0004t0018g0066 | 2 | HG02647.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.-117-474G>A | FAM156A | ENSG00000268350.8 | transcript | ENST00000622447.5 | protein_coding | 2/2 | chrX | 52949179 | ||||||
chrX:52949195
|
CA | C | 1 | a0006c0002t0001g0083 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.-117-491delT | FAM156A | ENSG00000268350.8 | transcript | ENST00000622447.5 | protein_coding | 2/2 | chrX | 52949195 | ||||||
chrX:52949200
|
T | C | 5 | a0001c0001t0001g0012a0001c0001t0001g0014a0001c0001t0001g0034others(2): Show | 7 | HG00738.hp1 HG01255.hp1 HG01884.hp2 others(4): Show |
intron_variant | MODIFIER | c.-117-495A>G | FAM156A | ENSG00000268350.8 | transcript | ENST00000622447.5 | protein_coding | 2/2 | chrX | 52949200 | ||||||
chrX:52949299
|
G | GA | 22 | a0001c0001t0001g0026a0001c0001t0001g0034a0001c0001t0001g0038others(19): Show | 22 | HG00280.hp1 HG00639.hp1 HG00738.hp1 others(19): Show |
intron_variant | MODIFIER | c.-117-595dupT | FAM156A | ENSG00000268350.8 | transcript | ENST00000622447.5 | protein_coding | 2/2 | chrX | 52949299 | ||||||
chrX:52949299
|
GA | G | 9 | a0001c0001t0001g0052a0001c0001t0001g0053a0001c0001t0001g0062others(6): Show | 9 | HG00323.hp1 HG01081.hp2 HG01175.hp1 others(6): Show |
intron_variant | MODIFIER | c.-117-595delT | FAM156A | ENSG00000268350.8 | transcript | ENST00000622447.5 | protein_coding | 2/2 | chrX | 52949299 | ||||||
chrX:52949313
|
A | AAAAAG | 1 | a0001c0001t0001g0077 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.-117-613_-117-609d others(7): Show |
FAM156A | ENSG00000268350.8 | transcript | ENST00000622447.5 | protein_coding | 2/2 | chrX | 52949313 | ||||||
chrX:52949373
|
G | GA | 1 | a0001c0001t0001g0034 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.-117-669dupT | FAM156A | ENSG00000268350.8 | transcript | ENST00000622447.5 | protein_coding | 2/2 | chrX | 52949373 | ||||||
chrX:52949684
|
G | A | 1 | a0001c0001t0001g0038 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.-117-979C>T | FAM156A | ENSG00000268350.8 | transcript | ENST00000622447.5 | protein_coding | 2/2 | chrX | 52949684 | ||||||
chrX:52949712
|
A | G | 1 | a0001c0001t0006g0018 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.-117-1007T>C | FAM156A | ENSG00000268350.8 | transcript | ENST00000622447.5 | protein_coding | 2/2 | chrX | 52949712 | ||||||
chrX:52949747
|
GC | G | 1 | a0006c0002t0001g0083 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.-117-1043delG | FAM156A | ENSG00000268350.8 | transcript | ENST00000622447.5 | protein_coding | 2/2 | chrX | 52949747 | ||||||
chrX:52949890
|
A | AT | 1 | a0006c0002t0001g0083 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.-117-1186dupA | FAM156A | ENSG00000268350.8 | transcript | ENST00000622447.5 | protein_coding | 2/2 | chrX | 52949890 | ||||||
chrX:52949892
|
CA | C | 1 | a0001c0001t0002g0029 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.-117-1188delT | FAM156A | ENSG00000268350.8 | transcript | ENST00000622447.5 | protein_coding | 2/2 | chrX | 52949892 | ||||||
chrX:52949909
|
G | A | 1 | a0001c0001t0002g0068 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.-117-1204C>T | FAM156A | ENSG00000268350.8 | transcript | ENST00000622447.5 | protein_coding | 2/2 | chrX | 52949909 | ||||||
chrX:52950298
|
A | T | 2 | a0001c0001t0001g0012a0001c0001t0001g0034 | 3 | HG01255.hp1 HG02809.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.-117-1593T>A | FAM156A | ENSG00000268350.8 | transcript | ENST00000622447.5 | protein_coding | 2/2 | chrX | 52950298 | ||||||
chrX:52950348
|
TC | T | 1 | a0001c0001t0020g0091 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.-117-1644delG | FAM156A | ENSG00000268350.8 | transcript | ENST00000622447.5 | protein_coding | 2/2 | chrX | 52950348 | ||||||
chrX:52950363
|
G | A | 2 | a0001c0001t0001g0046a0001c0001t0002g0041 | 2 | HG00323.hp2 NA18948.hp1 |
intron_variant | MODIFIER | c.-117-1658C>T | FAM156A | ENSG00000268350.8 | transcript | ENST00000622447.5 | protein_coding | 2/2 | chrX | 52950363 | ||||||
chrX:52950430
|
CG | C | 1 | a0006c0002t0001g0083 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.-117-1726delC | FAM156A | ENSG00000268350.8 | transcript | ENST00000622447.5 | protein_coding | 2/2 | chrX | 52950430 | ||||||
chrX:52950544
|
T | TC | 1 | a0001c0001t0003g0104 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.-117-1840dupG | FAM156A | ENSG00000268350.8 | transcript | ENST00000622447.5 | protein_coding | 2/2 | chrX | 52950544 | ||||||
chrX:52950563
|
TA | T | 1 | a0001c0001t0001g0024 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.-117-1859delT | FAM156A | ENSG00000268350.8 | transcript | ENST00000622447.5 | protein_coding | 2/2 | chrX | 52950563 | ||||||
chrX:52950658
|
T | TC | 1 | a0004c0005t0002g0045 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.-117-1954dupG | FAM156A | ENSG00000268350.8 | transcript | ENST00000622447.5 | protein_coding | 2/2 | chrX | 52950658 | ||||||
chrX:52950683
|
TGCAGTG | T | 1 | a0001c0001t0001g0047 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.-117-1984_-117-197 others(10): Show |
FAM156A | ENSG00000268350.8 | transcript | ENST00000622447.5 | protein_coding | 2/2 | chrX | 52950683 | ||||||
chrX:52950770
|
C | CA | 1 | a0001c0001t0002g0071 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.-117-2066dupT | FAM156A | ENSG00000268350.8 | transcript | ENST00000622447.5 | protein_coding | 2/2 | chrX | 52950770 | ||||||
chrX:52950770
|
CA | C | 1 | a0001c0001t0001g0077 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.-117-2066delT | FAM156A | ENSG00000268350.8 | transcript | ENST00000622447.5 | protein_coding | 2/2 | chrX | 52950770 | ||||||
chrX:52950838
|
A | C | 1 | a0001c0001t0002g0074 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.-117-2133T>G | FAM156A | ENSG00000268350.8 | transcript | ENST00000622447.5 | protein_coding | 2/2 | chrX | 52950838 | ||||||
chrX:52950839
|
T | A | 1 | a0001c0001t0002g0074 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.-117-2134A>T | FAM156A | ENSG00000268350.8 | transcript | ENST00000622447.5 | protein_coding | 2/2 | chrX | 52950839 | ||||||
chrX:52950841
|
G | T | 1 | a0001c0001t0002g0074 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.-117-2136C>A | FAM156A | ENSG00000268350.8 | transcript | ENST00000622447.5 | protein_coding | 2/2 | chrX | 52950841 | ||||||
chrX:52950846
|
T | C | 1 | a0001c0001t0002g0074 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.-117-2141A>G | FAM156A | ENSG00000268350.8 | transcript | ENST00000622447.5 | protein_coding | 2/2 | chrX | 52950846 | ||||||
chrX:52950848
|
CT | C | 1 | a0001c0001t0002g0074 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.-117-2144delA | FAM156A | ENSG00000268350.8 | transcript | ENST00000622447.5 | protein_coding | 2/2 | chrX | 52950848 | ||||||
chrX:52950851
|
G | T | 1 | a0001c0001t0002g0074 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.-117-2146C>A | FAM156A | ENSG00000268350.8 | transcript | ENST00000622447.5 | protein_coding | 2/2 | chrX | 52950851 | ||||||
chrX:52950852
|
C | G | 1 | a0001c0001t0002g0074 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.-117-2147G>C | FAM156A | ENSG00000268350.8 | transcript | ENST00000622447.5 | protein_coding | 2/2 | chrX | 52950852 | ||||||
chrX:52950880
|
G | GA | 1 | a0001c0001t0001g0042 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.-117-2176dupT | FAM156A | ENSG00000268350.8 | transcript | ENST00000622447.5 | protein_coding | 2/2 | chrX | 52950880 | ||||||
chrX:52950919
|
TC | T | 1 | a0001c0001t0002g0074 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.-117-2215delG | FAM156A | ENSG00000268350.8 | transcript | ENST00000622447.5 | protein_coding | 2/2 | chrX | 52950919 | ||||||
chrX:52950923
|
G | A | 23 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0014others(20): Show | 26 | HG00280.hp1 HG00639.hp1 HG00738.hp1 others(23): Show |
intron_variant | MODIFIER | c.-117-2218C>T | FAM156A | ENSG00000268350.8 | transcript | ENST00000622447.5 | protein_coding | 2/2 | chrX | 52950923 | ||||||
chrX:52950926
|
AGTTTT | A | 1 | a0001c0001t0002g0064 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.-117-2226_-117-222 others(9): Show |
FAM156A | ENSG00000268350.8 | transcript | ENST00000622447.5 | protein_coding | 2/2 | chrX | 52950926 | ||||||
chrX:52950932
|
G | C | 1 | a0001c0001t0002g0064 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.-117-2227C>G | FAM156A | ENSG00000268350.8 | transcript | ENST00000622447.5 | protein_coding | 2/2 | chrX | 52950932 | ||||||
chrX:52950936
|
T | C | 1 | a0001c0001t0002g0064 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.-117-2231A>G | FAM156A | ENSG00000268350.8 | transcript | ENST00000622447.5 | protein_coding | 2/2 | chrX | 52950936 | ||||||
chrX:52950936
|
TG | T | 2 | a0001c0001t0001g0077a0004c0005t0002g0045 | 2 | NA18982.hp1 NA19060.hp1 |
intron_variant | MODIFIER | c.-117-2232delC | FAM156A | ENSG00000268350.8 | transcript | ENST00000622447.5 | protein_coding | 2/2 | chrX | 52950936 | ||||||
chrX:52950938
|
G | C | 1 | a0001c0001t0002g0064 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.-117-2233C>G | FAM156A | ENSG00000268350.8 | transcript | ENST00000622447.5 | protein_coding | 2/2 | chrX | 52950938 | ||||||
chrX:52950939
|
G | GCGCTA | 1 | a0001c0001t0002g0064 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.-117-2235_-117-223 others(9): Show |
FAM156A | ENSG00000268350.8 | transcript | ENST00000622447.5 | protein_coding | 2/2 | chrX | 52950939 | ||||||
chrX:52950941
|
G | A | 1 | a0001c0001t0002g0064 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.-117-2236C>T | FAM156A | ENSG00000268350.8 | transcript | ENST00000622447.5 | protein_coding | 2/2 | chrX | 52950941 | ||||||
chrX:52950943
|
G | T | 1 | a0001c0001t0002g0064 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.-117-2238C>A | FAM156A | ENSG00000268350.8 | transcript | ENST00000622447.5 | protein_coding | 2/2 | chrX | 52950943 | ||||||
chrX:52951001
|
A | ACG | 1 | a0001c0001t0002g0063 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.-117-2298_-117-229 others(6): Show |
FAM156A | ENSG00000268350.8 | transcript | ENST00000622447.5 | protein_coding | 2/2 | chrX | 52951001 | ||||||
chrX:52951004
|
CA | C | 1 | a0001c0001t0004g0054 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.-117-2300delT | FAM156A | ENSG00000268350.8 | transcript | ENST00000622447.5 | protein_coding | 2/2 | chrX | 52951004 | ||||||
chrX:52951011
|
A | AT | 1 | a0001c0001t0002g0074 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.-117-2307dupA | FAM156A | ENSG00000268350.8 | transcript | ENST00000622447.5 | protein_coding | 2/2 | chrX | 52951011 | ||||||
chrX:52951096
|
G | GACAC | 1 | a0001c0001t0002g0074 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.-117-2392_-117-239 others(8): Show |
FAM156A | ENSG00000268350.8 | transcript | ENST00000622447.5 | protein_coding | 2/2 | chrX | 52951096 | ||||||
chrX:52951099
|
G | GA | 1 | a0001c0001t0004g0054 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.-117-2395dupT | FAM156A | ENSG00000268350.8 | transcript | ENST00000622447.5 | protein_coding | 2/2 | chrX | 52951099 | ||||||
chrX:52951101
|
A | T | 1 | a0001c0001t0002g0074 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.-117-2396T>A | FAM156A | ENSG00000268350.8 | transcript | ENST00000622447.5 | protein_coding | 2/2 | chrX | 52951101 | ||||||
chrX:52951102
|
A | C | 1 | a0001c0001t0002g0074 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.-117-2397T>G | FAM156A | ENSG00000268350.8 | transcript | ENST00000622447.5 | protein_coding | 2/2 | chrX | 52951102 | ||||||
chrX:52951103
|
C | G | 1 | a0001c0001t0002g0074 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.-117-2398G>C | FAM156A | ENSG00000268350.8 | transcript | ENST00000622447.5 | protein_coding | 2/2 | chrX | 52951103 | ||||||
chrX:52951106
|
TAGGA | T | 1 | a0001c0001t0002g0074 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.-117-2405_-117-240 others(8): Show |
FAM156A | ENSG00000268350.8 | transcript | ENST00000622447.5 | protein_coding | 2/2 | chrX | 52951106 | ||||||
chrX:52951112
|
G | T | 1 | a0001c0001t0002g0074 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.-117-2407C>A | FAM156A | ENSG00000268350.8 | transcript | ENST00000622447.5 | protein_coding | 2/2 | chrX | 52951112 | ||||||
chrX:52951113
|
A | T | 1 | a0001c0001t0002g0074 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.-117-2408T>A | FAM156A | ENSG00000268350.8 | transcript | ENST00000622447.5 | protein_coding | 2/2 | chrX | 52951113 | ||||||
chrX:52951200
|
T | TA | 1 | a0001c0001t0001g0040 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.-117-2496dupT | FAM156A | ENSG00000268350.8 | transcript | ENST00000622447.5 | protein_coding | 2/2 | chrX | 52951200 | ||||||
chrX:52951200
|
TA | T | 1 | a0001c0001t0002g0074 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.-117-2496delT | FAM156A | ENSG00000268350.8 | transcript | ENST00000622447.5 | protein_coding | 2/2 | chrX | 52951200 | ||||||
chrX:52951218
|
CG | C | 1 | a0001c0001t0004g0054 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.-117-2514delC | FAM156A | ENSG00000268350.8 | transcript | ENST00000622447.5 | protein_coding | 2/2 | chrX | 52951218 | ||||||
chrX:52951221
|
G | T | 1 | a0001c0001t0001g0034 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.-117-2516C>A | FAM156A | ENSG00000268350.8 | transcript | ENST00000622447.5 | protein_coding | 2/2 | chrX | 52951221 | ||||||
chrX:52951222
|
C | T | 1 | a0001c0001t0020g0091 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.-117-2517G>A | FAM156A | ENSG00000268350.8 | transcript | ENST00000622447.5 | protein_coding | 2/2 | chrX | 52951222 | ||||||
chrX:52951229
|
G | A | 1 | a0001c0001t0003g0102 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.-117-2524C>T | FAM156A | ENSG00000268350.8 | transcript | ENST00000622447.5 | protein_coding | 2/2 | chrX | 52951229 | ||||||
chrX:52951231
|
TC | T | 1 | a0001c0001t0021g0094 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.-117-2527delG | FAM156A | ENSG00000268350.8 | transcript | ENST00000622447.5 | protein_coding | 2/2 | chrX | 52951231 | ||||||
chrX:52951321
|
A | AC | 1 | a0001c0001t0002g0071 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.-117-2617dupG | FAM156A | ENSG00000268350.8 | transcript | ENST00000622447.5 | protein_coding | 2/2 | chrX | 52951321 | ||||||
chrX:52951334
|
CA | C | 1 | a0001c0001t0002g0063 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.-117-2630delT | FAM156A | ENSG00000268350.8 | transcript | ENST00000622447.5 | protein_coding | 2/2 | chrX | 52951334 | ||||||
chrX:52951369
|
T | A | 2 | a0001c0001t0002g0063a0001c0001t0016g0069 | 2 | NA18957.hp1 NA18969.hp1 |
intron_variant | MODIFIER | c.-117-2664A>T | FAM156A | ENSG00000268350.8 | transcript | ENST00000622447.5 | protein_coding | 2/2 | chrX | 52951369 | ||||||
chrX:52951378
|
T | TC | 1 | a0001c0001t0003g0104 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.-117-2674dupG | FAM156A | ENSG00000268350.8 | transcript | ENST00000622447.5 | protein_coding | 2/2 | chrX | 52951378 | ||||||
chrX:52951451
|
C | T | 1 | a0001c0001t0001g0075 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.-117-2746G>A | FAM156A | ENSG00000268350.8 | transcript | ENST00000622447.5 | protein_coding | 2/2 | chrX | 52951451 | ||||||
chrX:52951476
|
G | A | 9 | a0001c0001t0001g0006a0001c0001t0001g0016a0001c0001t0001g0022others(6): Show | 13 | HG01243.hp1 HG01884.hp1 HG01934.hp1 others(10): Show |
intron_variant | MODIFIER | c.-117-2771C>T | FAM156A | ENSG00000268350.8 | transcript | ENST00000622447.5 | protein_coding | 2/2 | chrX | 52951476 | ||||||
chrX:52951506
|
AAATAGAA others(3): Show |
A | 8 | a0001c0001t0003g0097a0001c0001t0003g0098a0001c0001t0003g0100others(5): Show | 8 | HG00280.hp1 HG00639.hp1 HG00741.hp1 others(5): Show |
intron_variant | MODIFIER | c.-117-2811_-117-280 others(14): Show |
FAM156A | ENSG00000268350.8 | transcript | ENST00000622447.5 | protein_coding | 2/2 | chrX | 52951506 | ||||||
chrX:52951554
|
A | G | 1 | a0001c0001t0008g0020 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.-117-2849T>C | FAM156A | ENSG00000268350.8 | transcript | ENST00000622447.5 | protein_coding | 2/2 | chrX | 52951554 | ||||||
chrX:52951580
|
A | C | 106 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(103): Show | 161 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(158): Show |
intron_variant | MODIFIER | c.-117-2875T>G | FAM156A | ENSG00000268350.8 | transcript | ENST00000622447.5 | protein_coding | 2/2 | chrX | 52951580 | ||||||
chrX:52951704
|
AG | A | 1 | a0001c0001t0004g0054 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.-117-3000delC | FAM156A | ENSG00000268350.8 | transcript | ENST00000622447.5 | protein_coding | 2/2 | chrX | 52951704 | ||||||
chrX:52951714
|
GT | G | 1 | a0001c0001t0001g0046 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.-117-3010delA | FAM156A | ENSG00000268350.8 | transcript | ENST00000622447.5 | protein_coding | 2/2 | chrX | 52951714 | ||||||
chrX:52951740
|
CTTA | C | 1 | a0001c0001t0001g0024 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.-117-3038_-117-303 others(7): Show |
FAM156A | ENSG00000268350.8 | transcript | ENST00000622447.5 | protein_coding | 2/2 | chrX | 52951740 | ||||||
chrX:52951748
|
C | CA | 1 | a0001c0001t0003g0103 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.-117-3044dupT | FAM156A | ENSG00000268350.8 | transcript | ENST00000622447.5 | protein_coding | 2/2 | chrX | 52951748 | ||||||
chrX:52951774
|
TC | T | 1 | a0001c0001t0001g0046 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.-117-3070delG | FAM156A | ENSG00000268350.8 | transcript | ENST00000622447.5 | protein_coding | 2/2 | chrX | 52951774 | ||||||
chrX:52951784
|
G | GA | 1 | a0001c0001t0002g0056 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.-117-3080dupT | FAM156A | ENSG00000268350.8 | transcript | ENST00000622447.5 | protein_coding | 2/2 | chrX | 52951784 | ||||||
chrX:52951798
|
C | CA | 1 | a0001c0001t0001g0025 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.-117-3094dupT | FAM156A | ENSG00000268350.8 | transcript | ENST00000622447.5 | protein_coding | 2/2 | chrX | 52951798 | ||||||
chrX:52951809
|
T | TG | 1 | a0001c0001t0002g0056 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.-117-3105dupC | FAM156A | ENSG00000268350.8 | transcript | ENST00000622447.5 | protein_coding | 2/2 | chrX | 52951809 | ||||||
chrX:52951809
|
TG | T | 4 | a0001c0001t0001g0062a0001c0001t0002g0063a0001c0001t0005g0093others(1): Show | 4 | HG02074.hp1 NA18969.hp1 NA18984.hp1 others(1): Show |
intron_variant | MODIFIER | c.-117-3105delC | FAM156A | ENSG00000268350.8 | transcript | ENST00000622447.5 | protein_coding | 2/2 | chrX | 52951809 | ||||||
chrX:52951836
|
A | AG | 1 | a0001c0001t0001g0044 | 1 | NA19004.hp1 | intron_variant | MODIFIER | c.-117-3132dupC | FAM156A | ENSG00000268350.8 | transcript | ENST00000622447.5 | protein_coding | 2/2 | chrX | 52951836 | ||||||
chrX:52951845
|
AT | A | 1 | a0001c0001t0001g0033 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.-117-3141delA | FAM156A | ENSG00000268350.8 | transcript | ENST00000622447.5 | protein_coding | 2/2 | chrX | 52951845 | ||||||
chrX:52951865
|
A | AG | 1 | a0001c0001t0002g0056 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.-117-3161dupC | FAM156A | ENSG00000268350.8 | transcript | ENST00000622447.5 | protein_coding | 2/2 | chrX | 52951865 | ||||||
chrX:52951907
|
C | CGAG | 1 | a0001c0001t0002g0071 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.-117-3205_-117-320 others(7): Show |
FAM156A | ENSG00000268350.8 | transcript | ENST00000622447.5 | protein_coding | 2/2 | chrX | 52951907 | ||||||
chrX:52952005
|
CA | C | 1 | a0001c0001t0021g0094 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.-118+3148delT | FAM156A | ENSG00000268350.8 | transcript | ENST00000622447.5 | protein_coding | 2/2 | chrX | 52952005 | ||||||
chrX:52952012
|
A | T | 1 | a0001c0001t0001g0044 | 1 | NA19004.hp1 | intron_variant | MODIFIER | c.-118+3142T>A | FAM156A | ENSG00000268350.8 | transcript | ENST00000622447.5 | protein_coding | 2/2 | chrX | 52952012 | ||||||
chrX:52952014
|
G | GT | 1 | a0001c0001t0001g0046 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.-118+3139dupA | FAM156A | ENSG00000268350.8 | transcript | ENST00000622447.5 | protein_coding | 2/2 | chrX | 52952014 | ||||||
chrX:52952035
|
TC | T | 2 | a0001c0001t0001g0046a0001c0001t0021g0094 | 2 | HG03688.hp1 NA18948.hp1 |
intron_variant | MODIFIER | c.-118+3118delG | FAM156A | ENSG00000268350.8 | transcript | ENST00000622447.5 | protein_coding | 2/2 | chrX | 52952035 | ||||||
chrX:52952045
|
G | A | 1 | a0001c0001t0001g0070 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.-118+3109C>T | FAM156A | ENSG00000268350.8 | transcript | ENST00000622447.5 | protein_coding | 2/2 | chrX | 52952045 | ||||||
chrX:52952053
|
A | AC | 1 | a0001c0001t0002g0074 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.-118+3100dupG | FAM156A | ENSG00000268350.8 | transcript | ENST00000622447.5 | protein_coding | 2/2 | chrX | 52952053 | ||||||
chrX:52952126
|
G | GC | 1 | a0001c0001t0002g0056 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.-118+3027dupG | FAM156A | ENSG00000268350.8 | transcript | ENST00000622447.5 | protein_coding | 2/2 | chrX | 52952126 | ||||||
chrX:52952126
|
GC | G | 1 | a0001c0001t0001g0062 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.-118+3027delG | FAM156A | ENSG00000268350.8 | transcript | ENST00000622447.5 | protein_coding | 2/2 | chrX | 52952126 | ||||||
chrX:52952228
|
T | TG | 1 | a0001c0001t0002g0074 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.-118+2925dupC | FAM156A | ENSG00000268350.8 | transcript | ENST00000622447.5 | protein_coding | 2/2 | chrX | 52952228 | ||||||
chrX:52952250
|
T | TC | 1 | a0001c0001t0003g0104 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.-118+2903dupG | FAM156A | ENSG00000268350.8 | transcript | ENST00000622447.5 | protein_coding | 2/2 | chrX | 52952250 | ||||||
chrX:52952258
|
G | GT | 1 | a0001c0001t0002g0056 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.-118+2895dupA | FAM156A | ENSG00000268350.8 | transcript | ENST00000622447.5 | protein_coding | 2/2 | chrX | 52952258 | ||||||
chrX:52952366
|
C | CT | 1 | a0001c0001t0002g0071 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.-118+2787dupA | FAM156A | ENSG00000268350.8 | transcript | ENST00000622447.5 | protein_coding | 2/2 | chrX | 52952366 | ||||||
chrX:52952393
|
A | AG | 1 | a0001c0001t0001g0044 | 1 | NA19004.hp1 | intron_variant | MODIFIER | c.-118+2760dupC | FAM156A | ENSG00000268350.8 | transcript | ENST00000622447.5 | protein_coding | 2/2 | chrX | 52952393 | ||||||
chrX:52952393
|
AG | A | 1 | a0001c0001t0021g0094 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.-118+2760delC | FAM156A | ENSG00000268350.8 | transcript | ENST00000622447.5 | protein_coding | 2/2 | chrX | 52952393 | ||||||
chrX:52952407
|
TG | T | 1 | a0001c0001t0002g0074 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.-118+2746delC | FAM156A | ENSG00000268350.8 | transcript | ENST00000622447.5 | protein_coding | 2/2 | chrX | 52952407 | ||||||
chrX:52952445
|
GT | G | 1 | a0001c0001t0002g0071 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.-118+2708delA | FAM156A | ENSG00000268350.8 | transcript | ENST00000622447.5 | protein_coding | 2/2 | chrX | 52952445 | ||||||
chrX:52952453
|
T | TC | 1 | a0001c0001t0001g0044 | 1 | NA19004.hp1 | intron_variant | MODIFIER | c.-118+2700dupG | FAM156A | ENSG00000268350.8 | transcript | ENST00000622447.5 | protein_coding | 2/2 | chrX | 52952453 | ||||||
chrX:52952453
|
TC | T | 1 | a0001c0001t0001g0022 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.-118+2700delG | FAM156A | ENSG00000268350.8 | transcript | ENST00000622447.5 | protein_coding | 2/2 | chrX | 52952453 | ||||||
chrX:52952457
|
G | A | 1 | a0001c0001t0001g0049 | 1 | HG01071.hp2 | intron_variant | MODIFIER | c.-118+2697C>T | FAM156A | ENSG00000268350.8 | transcript | ENST00000622447.5 | protein_coding | 2/2 | chrX | 52952457 | ||||||
chrX:52952552
|
G | GA | 2 | a0001c0001t0001g0022a0001c0001t0002g0056 | 2 | HG01243.hp1 HG02738.hp1 |
intron_variant | MODIFIER | c.-118+2601dupT | FAM156A | ENSG00000268350.8 | transcript | ENST00000622447.5 | protein_coding | 2/2 | chrX | 52952552 | ||||||
chrX:52952614
|
CT | C | 1 | a0001c0001t0001g0022 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.-118+2539delA | FAM156A | ENSG00000268350.8 | transcript | ENST00000622447.5 | protein_coding | 2/2 | chrX | 52952614 | ||||||
chrX:52952630
|
CA | C | 1 | a0001c0001t0001g0077 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.-118+2523delT | FAM156A | ENSG00000268350.8 | transcript | ENST00000622447.5 | protein_coding | 2/2 | chrX | 52952630 | ||||||
chrX:52952696
|
A | G | 1 | a0001c0001t0001g0034 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.-118+2458T>C | FAM156A | ENSG00000268350.8 | transcript | ENST00000622447.5 | protein_coding | 2/2 | chrX | 52952696 | ||||||
chrX:52952720
|
G | GT | 1 | a0001c0001t0001g0022 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.-118+2433dupA | FAM156A | ENSG00000268350.8 | transcript | ENST00000622447.5 | protein_coding | 2/2 | chrX | 52952720 | ||||||
chrX:52952751
|
G | GT | 1 | a0001c0001t0002g0074 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.-118+2402dupA | FAM156A | ENSG00000268350.8 | transcript | ENST00000622447.5 | protein_coding | 2/2 | chrX | 52952751 | ||||||
chrX:52952755
|
AT | A | 1 | a0001c0001t0001g0022 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.-118+2398delA | FAM156A | ENSG00000268350.8 | transcript | ENST00000622447.5 | protein_coding | 2/2 | chrX | 52952755 | ||||||
chrX:52952759
|
AC | A | 1 | a0001c0001t0002g0056 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.-118+2394delG | FAM156A | ENSG00000268350.8 | transcript | ENST00000622447.5 | protein_coding | 2/2 | chrX | 52952759 | ||||||
chrX:52952768
|
T | TA | 1 | a0001c0001t0002g0056 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.-118+2385_-118+238 others(5): Show |
FAM156A | ENSG00000268350.8 | transcript | ENST00000622447.5 | protein_coding | 2/2 | chrX | 52952768 | ||||||
chrX:52952777
|
GC | G | 1 | a0001c0001t0001g0022 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.-118+2376delG | FAM156A | ENSG00000268350.8 | transcript | ENST00000622447.5 | protein_coding | 2/2 | chrX | 52952777 | ||||||
chrX:52952785
|
TG | T | 1 | a0001c0001t0001g0062 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.-118+2368delC | FAM156A | ENSG00000268350.8 | transcript | ENST00000622447.5 | protein_coding | 2/2 | chrX | 52952785 | ||||||
chrX:52952838
|
C | CA | 3 | a0001c0001t0001g0014a0001c0001t0001g0037a0001c0001t0001g0038 | 4 | HG00738.hp1 HG01884.hp2 HG02486.hp1 others(1): Show |
intron_variant | MODIFIER | c.-118+2315dupT | FAM156A | ENSG00000268350.8 | transcript | ENST00000622447.5 | protein_coding | 2/2 | chrX | 52952838 | ||||||
chrX:52952863
|
A | AC | 1 | a0001c0001t0001g0022 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.-118+2290dupG | FAM156A | ENSG00000268350.8 | transcript | ENST00000622447.5 | protein_coding | 2/2 | chrX | 52952863 | ||||||
chrX:52952887
|
C | CT | 1 | a0001c0001t0001g0022 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.-118+2266dupA | FAM156A | ENSG00000268350.8 | transcript | ENST00000622447.5 | protein_coding | 2/2 | chrX | 52952887 | ||||||
chrX:52952940
|
T | A | 1 | a0001c0001t0001g0022 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.-118+2214A>T | FAM156A | ENSG00000268350.8 | transcript | ENST00000622447.5 | protein_coding | 2/2 | chrX | 52952940 | ||||||
chrX:52952960
|
CA | C | 1 | a0001c0001t0001g0022 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.-118+2193delT | FAM156A | ENSG00000268350.8 | transcript | ENST00000622447.5 | protein_coding | 2/2 | chrX | 52952960 | ||||||
chrX:52952968
|
TA | T | 1 | a0001c0001t0001g0022 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.-118+2185delT | FAM156A | ENSG00000268350.8 | transcript | ENST00000622447.5 | protein_coding | 2/2 | chrX | 52952968 | ||||||
chrX:52953010
|
T | TC | 1 | a0001c0001t0003g0104 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.-118+2143dupG | FAM156A | ENSG00000268350.8 | transcript | ENST00000622447.5 | protein_coding | 2/2 | chrX | 52953010 | ||||||
chrX:52953028
|
T | TG | 1 | a0001c0001t0021g0094 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.-118+2125dupC | FAM156A | ENSG00000268350.8 | transcript | ENST00000622447.5 | protein_coding | 2/2 | chrX | 52953028 | ||||||
chrX:52953101
|
AC | A | 2 | a0001c0001t0001g0077a0001c0001t0002g0072 | 2 | NA18982.hp1 NA18986.hp1 |
intron_variant | MODIFIER | c.-118+2052delG | FAM156A | ENSG00000268350.8 | transcript | ENST00000622447.5 | protein_coding | 2/2 | chrX | 52953101 | ||||||
chrX:52953107
|
A | AC | 1 | a0001c0001t0002g0056 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.-118+2046dupG | FAM156A | ENSG00000268350.8 | transcript | ENST00000622447.5 | protein_coding | 2/2 | chrX | 52953107 | ||||||
chrX:52953128
|
G | GT | 1 | a0001c0001t0001g0022 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.-118+2025dupA | FAM156A | ENSG00000268350.8 | transcript | ENST00000622447.5 | protein_coding | 2/2 | chrX | 52953128 | ||||||
chrX:52953301
|
A | AT | 1 | a0001c0001t0001g0023 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.-118+1852dupA | FAM156A | ENSG00000268350.8 | transcript | ENST00000622447.5 | protein_coding | 2/2 | chrX | 52953301 | ||||||
chrX:52953319
|
G | GT | 1 | a0001c0001t0002g0056 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.-118+1834dupA | FAM156A | ENSG00000268350.8 | transcript | ENST00000622447.5 | protein_coding | 2/2 | chrX | 52953319 | ||||||
chrX:52953329
|
G | GT | 1 | a0001c0001t0001g0040 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.-118+1824dupA | FAM156A | ENSG00000268350.8 | transcript | ENST00000622447.5 | protein_coding | 2/2 | chrX | 52953329 | ||||||
chrX:52953395
|
T | TG | 1 | a0001c0001t0002g0056 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.-118+1758dupC | FAM156A | ENSG00000268350.8 | transcript | ENST00000622447.5 | protein_coding | 2/2 | chrX | 52953395 | ||||||
chrX:52953398
|
G | C | 1 | a0001c0001t0001g0039 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.-118+1756C>G | FAM156A | ENSG00000268350.8 | transcript | ENST00000622447.5 | protein_coding | 2/2 | chrX | 52953398 | ||||||
chrX:52953435
|
CT | C | 1 | a0001c0001t0001g0025 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.-118+1718delA | FAM156A | ENSG00000268350.8 | transcript | ENST00000622447.5 | protein_coding | 2/2 | chrX | 52953435 | ||||||
chrX:52953458
|
C | CG | 2 | a0001c0001t0001g0046a0001c0001t0001g0073 | 2 | HG02145.hp1 NA18948.hp1 |
intron_variant | MODIFIER | c.-118+1695dupC | FAM156A | ENSG00000268350.8 | transcript | ENST00000622447.5 | protein_coding | 2/2 | chrX | 52953458 | ||||||
chrX:52953461
|
G | GT | 1 | a0001c0001t0002g0056 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.-118+1692dupA | FAM156A | ENSG00000268350.8 | transcript | ENST00000622447.5 | protein_coding | 2/2 | chrX | 52953461 | ||||||
chrX:52953483
|
T | TC | 1 | a0001c0001t0002g0056 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.-118+1670dupG | FAM156A | ENSG00000268350.8 | transcript | ENST00000622447.5 | protein_coding | 2/2 | chrX | 52953483 | ||||||
chrX:52953506
|
G | GC | 1 | a0001c0001t0001g0025 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.-118+1647dupG | FAM156A | ENSG00000268350.8 | transcript | ENST00000622447.5 | protein_coding | 2/2 | chrX | 52953506 | ||||||
chrX:52953563
|
G | A | 3 | a0001c0001t0004g0027a0001c0001t0004g0081a0001c0001t0004g0082 | 3 | HG01934.hp1 HG03139.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.-118+1591C>T | FAM156A | ENSG00000268350.8 | transcript | ENST00000622447.5 | protein_coding | 2/2 | chrX | 52953563 | ||||||
chrX:52953582
|
C | CA | 1 | a0004c0005t0002g0045 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.-118+1571dupT | FAM156A | ENSG00000268350.8 | transcript | ENST00000622447.5 | protein_coding | 2/2 | chrX | 52953582 | ||||||
chrX:52953595
|
TG | T | 1 | a0001c0001t0001g0025 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.-118+1558delC | FAM156A | ENSG00000268350.8 | transcript | ENST00000622447.5 | protein_coding | 2/2 | chrX | 52953595 | ||||||
chrX:52953616
|
G | GTAA | 1 | a0001c0001t0002g0056 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.-118+1535_-118+153 others(7): Show |
FAM156A | ENSG00000268350.8 | transcript | ENST00000622447.5 | protein_coding | 2/2 | chrX | 52953616 | ||||||
chrX:52953660
|
AC | A | 1 | a0001c0001t0001g0025 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.-118+1493delG | FAM156A | ENSG00000268350.8 | transcript | ENST00000622447.5 | protein_coding | 2/2 | chrX | 52953660 | ||||||
chrX:52953727
|
A | AG | 1 | a0001c0001t0001g0022 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.-118+1426dupC | FAM156A | ENSG00000268350.8 | transcript | ENST00000622447.5 | protein_coding | 2/2 | chrX | 52953727 | ||||||
chrX:52953738
|
C | CA | 35 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0014others(32): Show | 72 | HG00323.hp2 HG00544.hp1 HG00544.hp2 others(69): Show |
intron_variant | MODIFIER | c.-118+1415dupT | FAM156A | ENSG00000268350.8 | transcript | ENST00000622447.5 | protein_coding | 2/2 | chrX | 52953738 | ||||||
chrX:52953738
|
C | CAA | 20 | a0001c0001t0001g0005a0001c0001t0001g0017a0001c0001t0001g0023others(17): Show | 26 | HG00735.hp1 HG00735.hp2 HG01099.hp1 others(23): Show |
intron_variant | MODIFIER | c.-118+1414_-118+141 others(6): Show |
FAM156A | ENSG00000268350.8 | transcript | ENST00000622447.5 | protein_coding | 2/2 | chrX | 52953738 | ||||||
chrX:52953738
|
C | CAAA | 3 | a0001c0001t0001g0015a0001c0001t0001g0024a0001c0001t0001g0049 | 4 | HG01071.hp1 HG01071.hp2 HG01928.hp1 others(1): Show |
intron_variant | MODIFIER | c.-118+1413_-118+141 others(7): Show |
FAM156A | ENSG00000268350.8 | transcript | ENST00000622447.5 | protein_coding | 2/2 | chrX | 52953738 | ||||||
chrX:52953738
|
C | CAAAA | 1 | a0001c0001t0001g0050 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.-118+1412_-118+141 others(8): Show |
FAM156A | ENSG00000268350.8 | transcript | ENST00000622447.5 | protein_coding | 2/2 | chrX | 52953738 | ||||||
chrX:52953738
|
CA | C | 4 | a0001c0001t0001g0034a0001c0001t0001g0051a0001c0001t0003g0099others(1): Show | 4 | HG01255.hp1 HG02280.hp1 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.-118+1415delT | FAM156A | ENSG00000268350.8 | transcript | ENST00000622447.5 | protein_coding | 2/2 | chrX | 52953738 | ||||||
chrX:52953738
|
CAA | C | 2 | a0001c0001t0003g0098a0001c0001t0003g0105 | 2 | HG00741.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.-118+1414_-118+141 others(6): Show |
FAM156A | ENSG00000268350.8 | transcript | ENST00000622447.5 | protein_coding | 2/2 | chrX | 52953738 | ||||||
chrX:52953738
|
CAAAAA | C | 1 | a0001c0001t0001g0009 | 2 | HG03195.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.-118+1411_-118+141 others(9): Show |
FAM156A | ENSG00000268350.8 | transcript | ENST00000622447.5 | protein_coding | 2/2 | chrX | 52953738 | ||||||
chrX:52953738
|
CAAAAAAA | C | 3 | a0001c0001t0001g0022a0001c0001t0001g0031a0001c0001t0001g0078 | 3 | HG01069.hp1 HG01243.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.-118+1409_-118+141 others(11): Show |
FAM156A | ENSG00000268350.8 | transcript | ENST00000622447.5 | protein_coding | 2/2 | chrX | 52953738 | ||||||
chrX:52953738
|
CAAAAAAA others(1): Show |
C | 11 | a0001c0001t0001g0007a0001c0001t0001g0010a0001c0001t0001g0057others(8): Show | 15 | HG00597.hp1 HG00639.hp2 HG01515.hp1 others(12): Show |
intron_variant | MODIFIER | c.-118+1408_-118+141 others(12): Show |
FAM156A | ENSG00000268350.8 | transcript | ENST00000622447.5 | protein_coding | 2/2 | chrX | 52953738 | ||||||
chrX:52953738
|
CAAAAAAA others(2): Show |
C | 2 | a0001c0001t0001g0032a0001c0001t0001g0033 | 2 | HG00673.hp1 HG04204.hp1 |
intron_variant | MODIFIER | c.-118+1407_-118+141 others(13): Show |
FAM156A | ENSG00000268350.8 | transcript | ENST00000622447.5 | protein_coding | 2/2 | chrX | 52953738 | ||||||
chrX:52953738
|
CAAAAAAA others(4): Show |
C | 1 | a0001c0001t0003g0097 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.-118+1405_-118+141 others(15): Show |
FAM156A | ENSG00000268350.8 | transcript | ENST00000622447.5 | protein_coding | 2/2 | chrX | 52953738 | ||||||
chrX:52953738
|
CAAAAAAA others(5): Show |
C | 3 | a0001c0001t0001g0087a0001c0001t0002g0059a0001c0001t0002g0088 | 3 | HG01167.hp1 HG01169.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.-118+1404_-118+141 others(16): Show |
FAM156A | ENSG00000268350.8 | transcript | ENST00000622447.5 | protein_coding | 2/2 | chrX | 52953738 | ||||||
chrX:52953759
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A | G | 1 | a0001c0001t0001g0057 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.-118+1395T>C | FAM156A | ENSG00000268350.8 | transcript | ENST00000622447.5 | protein_coding | 2/2 | chrX | 52953759 | ||||||
chrX:52953763
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A | G | 9 | a0001c0001t0001g0007a0001c0001t0001g0010a0001c0001t0001g0031others(6): Show | 13 | HG00597.hp1 HG00639.hp2 HG01069.hp1 others(10): Show |
intron_variant | MODIFIER | c.-118+1391T>C | FAM156A | ENSG00000268350.8 | transcript | ENST00000622447.5 | protein_coding | 2/2 | chrX | 52953763 | ||||||
chrX:52953768
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G | A | 1 | a0001c0001t0001g0025 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.-118+1386C>T | FAM156A | ENSG00000268350.8 | transcript | ENST00000622447.5 | protein_coding | 2/2 | chrX | 52953768 | ||||||
chrX:52953769
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A | AAAG | 1 | a0001c0001t0001g0025 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.-118+1384_-118+138 others(7): Show |
FAM156A | ENSG00000268350.8 | transcript | ENST00000622447.5 | protein_coding | 2/2 | chrX | 52953769 | ||||||
chrX:52953774
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GA | G | 1 | a0001c0001t0002g0056 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.-118+1379delT | FAM156A | ENSG00000268350.8 | transcript | ENST00000622447.5 | protein_coding | 2/2 | chrX | 52953774 | ||||||
chrX:52953827
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T | C | 5 | a0001c0001t0001g0006a0001c0001t0001g0016a0001c0001t0001g0051others(2): Show | 9 | HG01884.hp1 HG02280.hp1 HG02615.hp2 others(6): Show |
intron_variant | MODIFIER | c.-118+1327A>G | FAM156A | ENSG00000268350.8 | transcript | ENST00000622447.5 | protein_coding | 2/2 | chrX | 52953827 | ||||||
chrX:52953900
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T | C | 1 | a0001c0001t0003g0106 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.-118+1254A>G | FAM156A | ENSG00000268350.8 | transcript | ENST00000622447.5 | protein_coding | 2/2 | chrX | 52953900 | ||||||
chrX:52953946
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G | T | 3 | a0001c0001t0002g0029a0001c0001t0008g0020a0001c0001t0010g0055 | 3 | HG03098.hp1 HG03579.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.-118+1208C>A | FAM156A | ENSG00000268350.8 | transcript | ENST00000622447.5 | protein_coding | 2/2 | chrX | 52953946 | ||||||
chrX:52953948
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TC | T | 1 | a0001c0001t0002g0056 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.-118+1205delG | FAM156A | ENSG00000268350.8 | transcript | ENST00000622447.5 | protein_coding | 2/2 | chrX | 52953948 | ||||||
chrX:52953963
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T | A | 1 | a0001c0001t0001g0025 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.-118+1191A>T | FAM156A | ENSG00000268350.8 | transcript | ENST00000622447.5 | protein_coding | 2/2 | chrX | 52953963 | ||||||
chrX:52954138
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G | GT | 1 | a0001c0001t0004g0082 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.-118+1015dupA | FAM156A | ENSG00000268350.8 | transcript | ENST00000622447.5 | protein_coding | 2/2 | chrX | 52954138 | ||||||
chrX:52954149
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C | A | 1 | a0001c0001t0001g0079 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.-118+1005G>T | FAM156A | ENSG00000268350.8 | transcript | ENST00000622447.5 | protein_coding | 2/2 | chrX | 52954149 | ||||||
chrX:52954153
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T | TC | 1 | a0001c0001t0004g0082 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.-118+1000dupG | FAM156A | ENSG00000268350.8 | transcript | ENST00000622447.5 | protein_coding | 2/2 | chrX | 52954153 | ||||||
chrX:52954267
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A | C | 3 | a0001c0001t0001g0009a0001c0001t0001g0023a0001c0001t0001g0028 | 4 | HG00735.hp1 HG02258.hp1 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.-118+887T>G | FAM156A | ENSG00000268350.8 | transcript | ENST00000622447.5 | protein_coding | 2/2 | chrX | 52954267 | ||||||
chrX:52954287
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G | A | 1 | a0001c0001t0001g0086 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.-118+867C>T | FAM156A | ENSG00000268350.8 | transcript | ENST00000622447.5 | protein_coding | 2/2 | chrX | 52954287 | ||||||
chrX:52954443
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A | AG | 1 | a0001c0001t0004g0082 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.-118+710dupC | FAM156A | ENSG00000268350.8 | transcript | ENST00000622447.5 | protein_coding | 2/2 | chrX | 52954443 | ||||||
chrX:52954512
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C | CG | 1 | a0001c0001t0001g0022 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.-118+641dupC | FAM156A | ENSG00000268350.8 | transcript | ENST00000622447.5 | protein_coding | 2/2 | chrX | 52954512 | ||||||
chrX:52954539
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T | TG | 1 | a0001c0001t0001g0080 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.-118+614dupC | FAM156A | ENSG00000268350.8 | transcript | ENST00000622447.5 | protein_coding | 2/2 | chrX | 52954539 | ||||||
chrX:52954612
|
TC | T | 1 | a0001c0001t0001g0025 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.-118+541delG | FAM156A | ENSG00000268350.8 | transcript | ENST00000622447.5 | protein_coding | 2/2 | chrX | 52954612 | ||||||
chrX:52954627
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TC | T | 1 | a0001c0001t0001g0025 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.-118+526delG | FAM156A | ENSG00000268350.8 | transcript | ENST00000622447.5 | protein_coding | 2/2 | chrX | 52954627 | ||||||
chrX:52954753
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G | GT | 1 | a0001c0001t0004g0082 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.-118+400dupA | FAM156A | ENSG00000268350.8 | transcript | ENST00000622447.5 | protein_coding | 2/2 | chrX | 52954753 | ||||||
chrX:52954831
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G | A | 2 | a0001c0001t0001g0052a0001c0001t0001g0053 | 2 | HG01081.hp2 HG01175.hp1 |
intron_variant | MODIFIER | c.-118+323C>T | FAM156A | ENSG00000268350.8 | transcript | ENST00000622447.5 | protein_coding | 2/2 | chrX | 52954831 | ||||||
chrX:52954841
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T | TG | 1 | a0001c0001t0001g0023 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.-118+312_-118+313i others(3): Show |
FAM156A | ENSG00000268350.8 | transcript | ENST00000622447.5 | protein_coding | 2/2 | chrX | 52954841 | ||||||
chrX:52954863
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AC | A | 1 | a0001c0001t0003g0105 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.-118+290delG | FAM156A | ENSG00000268350.8 | transcript | ENST00000622447.5 | protein_coding | 2/2 | chrX | 52954863 | ||||||
chrX:52954921
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T | TC | 1 | a0001c0001t0004g0082 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.-118+232dupG | FAM156A | ENSG00000268350.8 | transcript | ENST00000622447.5 | protein_coding | 2/2 | chrX | 52954921 | ||||||
chrX:52954965
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T | TC | 1 | a0001c0001t0001g0025 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.-118+188dupG | FAM156A | ENSG00000268350.8 | transcript | ENST00000622447.5 | protein_coding | 2/2 | chrX | 52954965 | ||||||
chrX:52955021
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TG | T | 1 | a0001c0001t0001g0025 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.-118+132delC | FAM156A | ENSG00000268350.8 | transcript | ENST00000622447.5 | protein_coding | 2/2 | chrX | 52955021 | ||||||
chrX:52955122
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C | CG | 1 | a0001c0001t0003g0106 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.-118+31dupC | FAM156A | ENSG00000268350.8 | transcript | ENST00000622447.5 | protein_coding | 2/2 | chrX | 52955122 | ||||||
chrX:52955122
|
CG | C | 1 | a0001c0001t0001g0024 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.-118+31delC | FAM156A | ENSG00000268350.8 | transcript | ENST00000622447.5 | protein_coding | 2/2 | chrX | 52955122 | ||||||
chrX:52955260
|
GA | G | 1 | a0001c0001t0004g0082 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.-210-15delT | FAM156A | ENSG00000268350.8 | transcript | ENST00000622447.5 | protein_coding | 1/2 | chrX | 52955260 | ||||||
chrX:52955292
|
G | T | 60 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0006others(57): Show | 88 | HG00280.hp1 HG00323.hp2 HG00544.hp2 others(85): Show |
intron_variant | MODIFIER | c.-210-46C>A | FAM156A | ENSG00000268350.8 | transcript | ENST00000622447.5 | protein_coding | 1/2 | chrX | 52955292 | ||||||
chrX:52955306
|
G | GAGCGC | 1 | a0001c0001t0001g0025 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.-210-65_-210-61dup others(5): Show |
FAM156A | ENSG00000268350.8 | transcript | ENST00000622447.5 | protein_coding | 1/2 | chrX | 52955306 | ||||||
chrX:52955327
|
G | GT | 1 | a0001c0001t0004g0082 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.-210-82dupA | FAM156A | ENSG00000268350.8 | transcript | ENST00000622447.5 | protein_coding | 1/2 | chrX | 52955327 | ||||||
chrX:52955336
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CA | C | 1 | a0001c0001t0006g0018 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.-210-91delT | FAM156A | ENSG00000268350.8 | transcript | ENST00000622447.5 | protein_coding | 1/2 | chrX | 52955336 | ||||||
chrX:52955362
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C | CT | 1 | a0001c0001t0003g0097 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.-210-117dupA | FAM156A | ENSG00000268350.8 | transcript | ENST00000622447.5 | protein_coding | 1/2 | chrX | 52955362 | ||||||
chrX:52955375
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TC | T | 1 | a0001c0001t0001g0025 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.-210-130delG | FAM156A | ENSG00000268350.8 | transcript | ENST00000622447.5 | protein_coding | 1/2 | chrX | 52955375 | ||||||
chrX:52955379
|
C | CA | 1 | a0001c0001t0004g0082 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.-210-134dupT | FAM156A | ENSG00000268350.8 | transcript | ENST00000622447.5 | protein_coding | 1/2 | chrX | 52955379 | ||||||
chrX:52955441
|
TC | T | 2 | a0001c0001t0001g0025a0001c0001t0023g0096 | 2 | HG02074.hp1 NA18989.hp1 |
intron_variant | MODIFIER | c.-210-196delG | FAM156A | ENSG00000268350.8 | transcript | ENST00000622447.5 | protein_coding | 1/2 | chrX | 52955441 | ||||||
chrX:52955458
|
C | CT | 2 | a0001c0001t0001g0026a0001c0001t0004g0027 | 2 | HG01934.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.-210-213dupA | FAM156A | ENSG00000268350.8 | transcript | ENST00000622447.5 | protein_coding | 1/2 | chrX | 52955458 | ||||||
chrX:52955458
|
CT | C | 7 | a0001c0001t0001g0025a0001c0001t0001g0084a0001c0001t0001g0086others(4): Show | 7 | HG01169.hp1 HG01169.hp2 HG01515.hp1 others(4): Show |
intron_variant | MODIFIER | c.-210-213delA | FAM156A | ENSG00000268350.8 | transcript | ENST00000622447.5 | protein_coding | 1/2 | chrX | 52955458 | ||||||
chrX:52955612
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A | AC | 2 | a0001c0001t0001g0024a0001c0001t0001g0025 | 2 | NA18989.hp1 NA19091.hp1 |
intron_variant | MODIFIER | c.-210-367dupG | FAM156A | ENSG00000268350.8 | transcript | ENST00000622447.5 | protein_coding | 1/2 | chrX | 52955612 | ||||||
chrX:52955696
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G | GC | 1 | a0001c0001t0003g0106 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.-210-451dupG | FAM156A | ENSG00000268350.8 | transcript | ENST00000622447.5 | protein_coding | 1/2 | chrX | 52955696 | ||||||
chrX:52955748
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CG | C | 1 | a0001c0001t0001g0089 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.-210-503delC | FAM156A | ENSG00000268350.8 | transcript | ENST00000622447.5 | protein_coding | 1/2 | chrX | 52955748 | ||||||
chrX:52955867
|
GA | G | 1 | a0001c0001t0006g0018 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.-211+405delT | FAM156A | ENSG00000268350.8 | transcript | ENST00000622447.5 | protein_coding | 1/2 | chrX | 52955867 | ||||||
chrX:52955900
|
AT | A | 1 | a0001c0001t0001g0023 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.-211+372delA | FAM156A | ENSG00000268350.8 | transcript | ENST00000622447.5 | protein_coding | 1/2 | chrX | 52955900 | ||||||
chrX:52956023
|
CA | C | 1 | a0001c0001t0006g0018 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.-211+249delT | FAM156A | ENSG00000268350.8 | transcript | ENST00000622447.5 | protein_coding | 1/2 | chrX | 52956023 | ||||||
chrX:52956112
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A | AT | 1 | a0001c0001t0001g0023 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.-211+160dupA | FAM156A | ENSG00000268350.8 | transcript | ENST00000622447.5 | protein_coding | 1/2 | chrX | 52956112 | ||||||
chrX:52956122
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T | C | 1 | a0001c0001t0001g0022 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.-211+151A>G | FAM156A | ENSG00000268350.8 | transcript | ENST00000622447.5 | protein_coding | 1/2 | chrX | 52956122 | ||||||
chrX:52956169
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TC | T | 1 | a0001c0001t0001g0022 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.-211+103delG | FAM156A | ENSG00000268350.8 | transcript | ENST00000622447.5 | protein_coding | 1/2 | chrX | 52956169 |