geneid | 54954 |
---|---|
ensemblid | ENSG00000184083.12 |
hgncid | 16949 |
symbol | FAM120C |
name | family with sequence similarity 120C |
refseq_nuc | NM_017848.6 |
refseq_prot | NP_060318.4 |
ensembl_nuc | ENST00000375180.7 |
ensembl_prot | ENSP00000364324.2 |
mane_status | MANE Select |
chr | chrX |
start | 54068324 |
end | 54183254 |
strand | - |
ver | v1.2 |
region | chrX:54068324-54183254 |
region5000 | chrX:54063324-54188254 |
regionname0 | FAM120C_chrX_54068324_54183254 |
regionname5000 | FAM120C_chrX_54063324_54188254 |
ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 1/1 | 1096 | 179 | 47 | 28 | 83 | 3 | 16 | 66 | FAM120C_chrX_54063324_54188254 | FAM120C | copy fasta | chrX | 54063324 | 54188254 |
a0002 | 0/0 | 1098 | 4 | 0 | 3 | 0 | 1 | 0 | 0 | FAM120C_chrX_54063324_54188254 | FAM120C | copy fasta | chrX | 54063324 | 54188254 |
a0003 | 0/0 | 1096 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | FAM120C_chrX_54063324_54188254 | FAM120C | copy fasta | chrX | 54063324 | 54188254 |
a0004 | 0/0 | 1096 | 1 | 0 | 0 | 0 | 1 | 0 | 0 | FAM120C_chrX_54063324_54188254 | FAM120C | copy fasta | chrX | 54063324 | 54188254 |
a0005 | 0/0 | 511 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | FAM120C_chrX_54063324_54188254 | FAM120C | copy fasta | chrX | 54063324 | 54188254 |
a0006 | 0/0 | 573 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | FAM120C_chrX_54063324_54188254 | FAM120C | copy fasta | chrX | 54063324 | 54188254 |
a0007 | 0/0 | 1096 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | FAM120C_chrX_54063324_54188254 | FAM120C | copy fasta | chrX | 54063324 | 54188254 |
a0008 | 0/0 | 196 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | FAM120C_chrX_54063324_54188254 | FAM120C | copy fasta | chrX | 54063324 | 54188254 |
chapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
c0001 | 1/1 | 3291 | 177 | 47 | 28 | 81 | 3 | 16 | FAM120C_chrX_54063324_54188254 | FAM120C | copy fasta | chrX | 54063324 | 54188254 |
c0002 | 0/0 | 3297 | 4 | 0 | 3 | 0 | 1 | 0 | FAM120C_chrX_54063324_54188254 | FAM120C | copy fasta | chrX | 54063324 | 54188254 |
c0003 | 0/0 | 3291 | 2 | 2 | 0 | 0 | 0 | 0 | FAM120C_chrX_54063324_54188254 | FAM120C | copy fasta | chrX | 54063324 | 54188254 |
c0004 | 0/0 | 3291 | 1 | 1 | 0 | 0 | 0 | 0 | FAM120C_chrX_54063324_54188254 | FAM120C | copy fasta | chrX | 54063324 | 54188254 |
c0005 | 0/0 | 3291 | 1 | 0 | 0 | 1 | 0 | 0 | FAM120C_chrX_54063324_54188254 | FAM120C | copy fasta | chrX | 54063324 | 54188254 |
c0006 | 0/0 | 3290 | 1 | 0 | 0 | 1 | 0 | 0 | FAM120C_chrX_54063324_54188254 | FAM120C | copy fasta | chrX | 54063324 | 54188254 |
c0007 | 0/0 | 3288 | 1 | 0 | 0 | 1 | 0 | 0 | FAM120C_chrX_54063324_54188254 | FAM120C | copy fasta | chrX | 54063324 | 54188254 |
c0008 | 0/0 | 3291 | 1 | 0 | 0 | 0 | 1 | 0 | FAM120C_chrX_54063324_54188254 | FAM120C | copy fasta | chrX | 54063324 | 54188254 |
c0009 | 0/0 | 3291 | 1 | 0 | 0 | 1 | 0 | 0 | FAM120C_chrX_54063324_54188254 | FAM120C | copy fasta | chrX | 54063324 | 54188254 |
c0010 | 0/0 | 3293 | 1 | 0 | 0 | 1 | 0 | 0 | FAM120C_chrX_54063324_54188254 | FAM120C | copy fasta | chrX | 54063324 | 54188254 |
thapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
t0001 | 0/0 | 4768 | 16 | 0 | 2 | 13 | 1 | 0 | FAM120C_chrX_54063324_54188254 | FAM120C | copy fasta | chrX | 54063324 | 54188254 |
t0002 | 0/1 | 4753 | 11 | 0 | 1 | 9 | 0 | 0 | FAM120C_chrX_54063324_54188254 | FAM120C | copy fasta | chrX | 54063324 | 54188254 |
t0003 | 0/0 | 4758 | 9 | 1 | 3 | 3 | 0 | 2 | FAM120C_chrX_54063324_54188254 | FAM120C | copy fasta | chrX | 54063324 | 54188254 |
t0004 | 0/0 | 4766 | 7 | 0 | 5 | 2 | 0 | 0 | FAM120C_chrX_54063324_54188254 | FAM120C | copy fasta | chrX | 54063324 | 54188254 |
t0005 | 0/0 | 4770 | 7 | 0 | 0 | 7 | 0 | 0 | FAM120C_chrX_54063324_54188254 | FAM120C | copy fasta | chrX | 54063324 | 54188254 |
t0006 | 0/0 | 4754 | 6 | 0 | 0 | 6 | 0 | 0 | FAM120C_chrX_54063324_54188254 | FAM120C | copy fasta | chrX | 54063324 | 54188254 |
t0007 | 0/0 | 4769 | 6 | 0 | 1 | 5 | 0 | 0 | FAM120C_chrX_54063324_54188254 | FAM120C | copy fasta | chrX | 54063324 | 54188254 |
t0008 | 0/0 | 4751 | 6 | 2 | 0 | 4 | 0 | 0 | FAM120C_chrX_54063324_54188254 | FAM120C | copy fasta | chrX | 54063324 | 54188254 |
t0009 | 0/0 | 4773 | 6 | 0 | 1 | 3 | 1 | 1 | FAM120C_chrX_54063324_54188254 | FAM120C | copy fasta | chrX | 54063324 | 54188254 |
t0010 | 0/0 | 4772 | 6 | 0 | 0 | 6 | 0 | 0 | FAM120C_chrX_54063324_54188254 | FAM120C | copy fasta | chrX | 54063324 | 54188254 |
t0011 | 0/0 | 4756 | 5 | 1 | 2 | 2 | 0 | 0 | FAM120C_chrX_54063324_54188254 | FAM120C | copy fasta | chrX | 54063324 | 54188254 |
t0012 | 0/0 | 4756 | 5 | 0 | 0 | 2 | 0 | 3 | FAM120C_chrX_54063324_54188254 | FAM120C | copy fasta | chrX | 54063324 | 54188254 |
t0013 | 0/0 | 4774 | 4 | 4 | 0 | 0 | 0 | 0 | FAM120C_chrX_54063324_54188254 | FAM120C | copy fasta | chrX | 54063324 | 54188254 |
t0014 | 0/0 | 4754 | 4 | 0 | 1 | 0 | 0 | 3 | FAM120C_chrX_54063324_54188254 | FAM120C | copy fasta | chrX | 54063324 | 54188254 |
t0015 | 0/0 | 4776 | 4 | 4 | 0 | 0 | 0 | 0 | FAM120C_chrX_54063324_54188254 | FAM120C | copy fasta | chrX | 54063324 | 54188254 |
t0016 | 0/0 | 4763 | 4 | 4 | 0 | 0 | 0 | 0 | FAM120C_chrX_54063324_54188254 | FAM120C | copy fasta | chrX | 54063324 | 54188254 |
t0017 | 0/0 | 4755 | 4 | 1 | 3 | 0 | 0 | 0 | FAM120C_chrX_54063324_54188254 | FAM120C | copy fasta | chrX | 54063324 | 54188254 |
t0018 | 0/0 | 4766 | 3 | 3 | 0 | 0 | 0 | 0 | FAM120C_chrX_54063324_54188254 | FAM120C | copy fasta | chrX | 54063324 | 54188254 |
t0019 | 0/0 | 4769 | 3 | 2 | 1 | 0 | 0 | 0 | FAM120C_chrX_54063324_54188254 | FAM120C | copy fasta | chrX | 54063324 | 54188254 |
t0020 | 0/0 | 4749 | 3 | 2 | 1 | 0 | 0 | 0 | FAM120C_chrX_54063324_54188254 | FAM120C | copy fasta | chrX | 54063324 | 54188254 |
t0021 | 0/0 | 4764 | 3 | 0 | 0 | 3 | 0 | 0 | FAM120C_chrX_54063324_54188254 | FAM120C | copy fasta | chrX | 54063324 | 54188254 |
t0022 | 0/0 | 4781 | 3 | 3 | 0 | 0 | 0 | 0 | FAM120C_chrX_54063324_54188254 | FAM120C | copy fasta | chrX | 54063324 | 54188254 |
t0023 | 0/0 | 4763 | 3 | 0 | 1 | 1 | 1 | 0 | FAM120C_chrX_54063324_54188254 | FAM120C | copy fasta | chrX | 54063324 | 54188254 |
t0024 | 0/0 | 4762 | 2 | 0 | 0 | 1 | 0 | 1 | FAM120C_chrX_54063324_54188254 | FAM120C | copy fasta | chrX | 54063324 | 54188254 |
t0025 | 0/0 | 4776 | 2 | 2 | 0 | 0 | 0 | 0 | FAM120C_chrX_54063324_54188254 | FAM120C | copy fasta | chrX | 54063324 | 54188254 |
t0026 | 0/0 | 4771 | 2 | 2 | 0 | 0 | 0 | 0 | FAM120C_chrX_54063324_54188254 | FAM120C | copy fasta | chrX | 54063324 | 54188254 |
t0027 | 0/0 | 4766 | 2 | 2 | 0 | 0 | 0 | 0 | FAM120C_chrX_54063324_54188254 | FAM120C | copy fasta | chrX | 54063324 | 54188254 |
t0028 | 0/0 | 4771 | 2 | 0 | 1 | 0 | 1 | 0 | FAM120C_chrX_54063324_54188254 | FAM120C | copy fasta | chrX | 54063324 | 54188254 |
t0029 | 0/0 | 4761 | 2 | 0 | 0 | 0 | 1 | 1 | FAM120C_chrX_54063324_54188254 | FAM120C | copy fasta | chrX | 54063324 | 54188254 |
t0030 | 0/0 | 4773 | 2 | 2 | 0 | 0 | 0 | 0 | FAM120C_chrX_54063324_54188254 | FAM120C | copy fasta | chrX | 54063324 | 54188254 |
t0031 | 0/0 | 4768 | 2 | 1 | 1 | 0 | 0 | 0 | FAM120C_chrX_54063324_54188254 | FAM120C | copy fasta | chrX | 54063324 | 54188254 |
t0032 | 0/0 | 4748 | 2 | 0 | 0 | 2 | 0 | 0 | FAM120C_chrX_54063324_54188254 | FAM120C | copy fasta | chrX | 54063324 | 54188254 |
t0033 | 0/0 | 4781 | 2 | 2 | 0 | 0 | 0 | 0 | FAM120C_chrX_54063324_54188254 | FAM120C | copy fasta | chrX | 54063324 | 54188254 |
t0034 | 0/0 | 4776 | 1 | 0 | 0 | 1 | 0 | 0 | FAM120C_chrX_54063324_54188254 | FAM120C | copy fasta | chrX | 54063324 | 54188254 |
t0035 | 0/0 | 4763 | 1 | 0 | 0 | 1 | 0 | 0 | FAM120C_chrX_54063324_54188254 | FAM120C | copy fasta | chrX | 54063324 | 54188254 |
t0036 | 0/0 | 4760 | 1 | 0 | 1 | 0 | 0 | 0 | FAM120C_chrX_54063324_54188254 | FAM120C | copy fasta | chrX | 54063324 | 54188254 |
t0037 | 0/0 | 4754 | 1 | 0 | 0 | 1 | 0 | 0 | FAM120C_chrX_54063324_54188254 | FAM120C | copy fasta | chrX | 54063324 | 54188254 |
t0038 | 0/0 | 4756 | 1 | 0 | 0 | 0 | 0 | 1 | FAM120C_chrX_54063324_54188254 | FAM120C | copy fasta | chrX | 54063324 | 54188254 |
t0039 | 0/0 | 4768 | 1 | 1 | 0 | 0 | 0 | 0 | FAM120C_chrX_54063324_54188254 | FAM120C | copy fasta | chrX | 54063324 | 54188254 |
t0040 | 1/0 | 4766 | 1 | 0 | 0 | 0 | 0 | 0 | FAM120C_chrX_54063324_54188254 | FAM120C | copy fasta | chrX | 54063324 | 54188254 |
t0041 | 0/0 | 4777 | 1 | 0 | 1 | 0 | 0 | 0 | FAM120C_chrX_54063324_54188254 | FAM120C | copy fasta | chrX | 54063324 | 54188254 |
t0042 | 0/0 | 4767 | 1 | 1 | 0 | 0 | 0 | 0 | FAM120C_chrX_54063324_54188254 | FAM120C | copy fasta | chrX | 54063324 | 54188254 |
t0043 | 0/0 | 4752 | 1 | 1 | 0 | 0 | 0 | 0 | FAM120C_chrX_54063324_54188254 | FAM120C | copy fasta | chrX | 54063324 | 54188254 |
t0044 | 0/0 | 4747 | 1 | 0 | 0 | 0 | 0 | 1 | FAM120C_chrX_54063324_54188254 | FAM120C | copy fasta | chrX | 54063324 | 54188254 |
t0045 | 0/0 | 4752 | 1 | 1 | 0 | 0 | 0 | 0 | FAM120C_chrX_54063324_54188254 | FAM120C | copy fasta | chrX | 54063324 | 54188254 |
t0046 | 0/0 | 4774 | 1 | 0 | 0 | 1 | 0 | 0 | FAM120C_chrX_54063324_54188254 | FAM120C | copy fasta | chrX | 54063324 | 54188254 |
t0047 | 0/0 | 4761 | 1 | 0 | 1 | 0 | 0 | 0 | FAM120C_chrX_54063324_54188254 | FAM120C | copy fasta | chrX | 54063324 | 54188254 |
t0048 | 0/0 | 4761 | 1 | 1 | 0 | 0 | 0 | 0 | FAM120C_chrX_54063324_54188254 | FAM120C | copy fasta | chrX | 54063324 | 54188254 |
t0049 | 0/0 | 4761 | 1 | 1 | 0 | 0 | 0 | 0 | FAM120C_chrX_54063324_54188254 | FAM120C | copy fasta | chrX | 54063324 | 54188254 |
t0050 | 0/0 | 4756 | 1 | 0 | 0 | 1 | 0 | 0 | FAM120C_chrX_54063324_54188254 | FAM120C | copy fasta | chrX | 54063324 | 54188254 |
t0051 | 0/0 | 4741 | 1 | 1 | 0 | 0 | 0 | 0 | FAM120C_chrX_54063324_54188254 | FAM120C | copy fasta | chrX | 54063324 | 54188254 |
t0052 | 0/0 | 4771 | 1 | 0 | 1 | 0 | 0 | 0 | FAM120C_chrX_54063324_54188254 | FAM120C | copy fasta | chrX | 54063324 | 54188254 |
t0053 | 0/0 | 4768 | 1 | 0 | 1 | 0 | 0 | 0 | FAM120C_chrX_54063324_54188254 | FAM120C | copy fasta | chrX | 54063324 | 54188254 |
t0054 | 0/0 | 4778 | 1 | 1 | 0 | 0 | 0 | 0 | FAM120C_chrX_54063324_54188254 | FAM120C | copy fasta | chrX | 54063324 | 54188254 |
t0055 | 0/0 | 4778 | 1 | 0 | 0 | 1 | 0 | 0 | FAM120C_chrX_54063324_54188254 | FAM120C | copy fasta | chrX | 54063324 | 54188254 |
t0056 | 0/0 | 4768 | 1 | 1 | 0 | 0 | 0 | 0 | FAM120C_chrX_54063324_54188254 | FAM120C | copy fasta | chrX | 54063324 | 54188254 |
t0057 | 0/0 | 4758 | 1 | 0 | 0 | 1 | 0 | 0 | FAM120C_chrX_54063324_54188254 | FAM120C | copy fasta | chrX | 54063324 | 54188254 |
t0058 | 0/0 | 4773 | 1 | 0 | 1 | 0 | 0 | 0 | FAM120C_chrX_54063324_54188254 | FAM120C | copy fasta | chrX | 54063324 | 54188254 |
t0059 | 0/0 | 4768 | 1 | 0 | 0 | 0 | 0 | 1 | FAM120C_chrX_54063324_54188254 | FAM120C | copy fasta | chrX | 54063324 | 54188254 |
t0060 | 0/0 | 4780 | 1 | 1 | 0 | 0 | 0 | 0 | FAM120C_chrX_54063324_54188254 | FAM120C | copy fasta | chrX | 54063324 | 54188254 |
t0061 | 0/0 | 4775 | 1 | 0 | 1 | 0 | 0 | 0 | FAM120C_chrX_54063324_54188254 | FAM120C | copy fasta | chrX | 54063324 | 54188254 |
t0062 | 0/0 | 4765 | 1 | 0 | 0 | 1 | 0 | 0 | FAM120C_chrX_54063324_54188254 | FAM120C | copy fasta | chrX | 54063324 | 54188254 |
t0063 | 0/0 | 4760 | 1 | 0 | 0 | 1 | 0 | 0 | FAM120C_chrX_54063324_54188254 | FAM120C | copy fasta | chrX | 54063324 | 54188254 |
t0064 | 0/0 | 4775 | 1 | 0 | 0 | 1 | 0 | 0 | FAM120C_chrX_54063324_54188254 | FAM120C | copy fasta | chrX | 54063324 | 54188254 |
t0065 | 0/0 | 4777 | 1 | 0 | 0 | 1 | 0 | 0 | FAM120C_chrX_54063324_54188254 | FAM120C | copy fasta | chrX | 54063324 | 54188254 |
t0066 | 0/0 | 4762 | 1 | 0 | 0 | 1 | 0 | 0 | FAM120C_chrX_54063324_54188254 | FAM120C | copy fasta | chrX | 54063324 | 54188254 |
t0067 | 0/0 | 4774 | 1 | 1 | 0 | 0 | 0 | 0 | FAM120C_chrX_54063324_54188254 | FAM120C | copy fasta | chrX | 54063324 | 54188254 |
t0068 | 0/0 | 4764 | 1 | 0 | 0 | 0 | 0 | 1 | FAM120C_chrX_54063324_54188254 | FAM120C | copy fasta | chrX | 54063324 | 54188254 |
t0069 | 0/0 | 4768 | 1 | 0 | 0 | 0 | 0 | 1 | FAM120C_chrX_54063324_54188254 | FAM120C | copy fasta | chrX | 54063324 | 54188254 |
t0070 | 0/0 | 4763 | 1 | 0 | 0 | 1 | 0 | 0 | FAM120C_chrX_54063324_54188254 | FAM120C | copy fasta | chrX | 54063324 | 54188254 |
t0071 | 0/0 | 4755 | 1 | 0 | 0 | 1 | 0 | 0 | FAM120C_chrX_54063324_54188254 | FAM120C | copy fasta | chrX | 54063324 | 54188254 |
t0072 | 0/0 | 4769 | 1 | 1 | 0 | 0 | 0 | 0 | FAM120C_chrX_54063324_54188254 | FAM120C | copy fasta | chrX | 54063324 | 54188254 |
t0073 | 0/0 | 4757 | 1 | 0 | 0 | 1 | 0 | 0 | FAM120C_chrX_54063324_54188254 | FAM120C | copy fasta | chrX | 54063324 | 54188254 |
t0074 | 0/0 | 4755 | 1 | 0 | 0 | 1 | 0 | 0 | FAM120C_chrX_54063324_54188254 | FAM120C | copy fasta | chrX | 54063324 | 54188254 |
t0075 | 0/0 | 4756 | 1 | 0 | 0 | 1 | 0 | 0 | FAM120C_chrX_54063324_54188254 | FAM120C | copy fasta | chrX | 54063324 | 54188254 |
ghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
g0001 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | FAM120C_chrX_54063324_54188254 | FAM120C | chrX | 54063324 | 54188254 |
g0002 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | FAM120C_chrX_54063324_54188254 | FAM120C | chrX | 54063324 | 54188254 |
g0003 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM120C_chrX_54063324_54188254 | FAM120C | chrX | 54063324 | 54188254 |
g0004 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM120C_chrX_54063324_54188254 | FAM120C | chrX | 54063324 | 54188254 |
g0005 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM120C_chrX_54063324_54188254 | FAM120C | chrX | 54063324 | 54188254 |
g0006 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM120C_chrX_54063324_54188254 | FAM120C | chrX | 54063324 | 54188254 |
g0007 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM120C_chrX_54063324_54188254 | FAM120C | chrX | 54063324 | 54188254 |
g0008 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM120C_chrX_54063324_54188254 | FAM120C | chrX | 54063324 | 54188254 |
g0009 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM120C_chrX_54063324_54188254 | FAM120C | chrX | 54063324 | 54188254 |
g0010 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM120C_chrX_54063324_54188254 | FAM120C | chrX | 54063324 | 54188254 |
g0011 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM120C_chrX_54063324_54188254 | FAM120C | chrX | 54063324 | 54188254 |
g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM120C_chrX_54063324_54188254 | FAM120C | chrX | 54063324 | 54188254 |
g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM120C_chrX_54063324_54188254 | FAM120C | chrX | 54063324 | 54188254 |
g0014 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM120C_chrX_54063324_54188254 | FAM120C | chrX | 54063324 | 54188254 |
g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM120C_chrX_54063324_54188254 | FAM120C | chrX | 54063324 | 54188254 |
g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM120C_chrX_54063324_54188254 | FAM120C | chrX | 54063324 | 54188254 |
g0017 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM120C_chrX_54063324_54188254 | FAM120C | chrX | 54063324 | 54188254 |
g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM120C_chrX_54063324_54188254 | FAM120C | chrX | 54063324 | 54188254 |
g0019 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM120C_chrX_54063324_54188254 | FAM120C | chrX | 54063324 | 54188254 |
g0020 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM120C_chrX_54063324_54188254 | FAM120C | chrX | 54063324 | 54188254 |
g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM120C_chrX_54063324_54188254 | FAM120C | chrX | 54063324 | 54188254 |
g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM120C_chrX_54063324_54188254 | FAM120C | chrX | 54063324 | 54188254 |
g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM120C_chrX_54063324_54188254 | FAM120C | chrX | 54063324 | 54188254 |
g0024 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM120C_chrX_54063324_54188254 | FAM120C | chrX | 54063324 | 54188254 |
g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM120C_chrX_54063324_54188254 | FAM120C | chrX | 54063324 | 54188254 |
g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM120C_chrX_54063324_54188254 | FAM120C | chrX | 54063324 | 54188254 |
g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM120C_chrX_54063324_54188254 | FAM120C | chrX | 54063324 | 54188254 |
g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM120C_chrX_54063324_54188254 | FAM120C | chrX | 54063324 | 54188254 |
g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM120C_chrX_54063324_54188254 | FAM120C | chrX | 54063324 | 54188254 |
g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM120C_chrX_54063324_54188254 | FAM120C | chrX | 54063324 | 54188254 |
g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM120C_chrX_54063324_54188254 | FAM120C | chrX | 54063324 | 54188254 |
g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM120C_chrX_54063324_54188254 | FAM120C | chrX | 54063324 | 54188254 |
g0033 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM120C_chrX_54063324_54188254 | FAM120C | chrX | 54063324 | 54188254 |
g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM120C_chrX_54063324_54188254 | FAM120C | chrX | 54063324 | 54188254 |
g0035 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM120C_chrX_54063324_54188254 | FAM120C | chrX | 54063324 | 54188254 |
g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM120C_chrX_54063324_54188254 | FAM120C | chrX | 54063324 | 54188254 |
g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM120C_chrX_54063324_54188254 | FAM120C | chrX | 54063324 | 54188254 |
g0038 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM120C_chrX_54063324_54188254 | FAM120C | chrX | 54063324 | 54188254 |
g0039 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | FAM120C_chrX_54063324_54188254 | FAM120C | chrX | 54063324 | 54188254 |
g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM120C_chrX_54063324_54188254 | FAM120C | chrX | 54063324 | 54188254 |
g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM120C_chrX_54063324_54188254 | FAM120C | chrX | 54063324 | 54188254 |
g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM120C_chrX_54063324_54188254 | FAM120C | chrX | 54063324 | 54188254 |
g0043 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM120C_chrX_54063324_54188254 | FAM120C | chrX | 54063324 | 54188254 |
g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM120C_chrX_54063324_54188254 | FAM120C | chrX | 54063324 | 54188254 |
g0045 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM120C_chrX_54063324_54188254 | FAM120C | chrX | 54063324 | 54188254 |
g0046 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM120C_chrX_54063324_54188254 | FAM120C | chrX | 54063324 | 54188254 |
g0047 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM120C_chrX_54063324_54188254 | FAM120C | chrX | 54063324 | 54188254 |
g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM120C_chrX_54063324_54188254 | FAM120C | chrX | 54063324 | 54188254 |
g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM120C_chrX_54063324_54188254 | FAM120C | chrX | 54063324 | 54188254 |
g0050 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM120C_chrX_54063324_54188254 | FAM120C | chrX | 54063324 | 54188254 |
g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM120C_chrX_54063324_54188254 | FAM120C | chrX | 54063324 | 54188254 |
g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM120C_chrX_54063324_54188254 | FAM120C | chrX | 54063324 | 54188254 |
g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM120C_chrX_54063324_54188254 | FAM120C | chrX | 54063324 | 54188254 |
g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM120C_chrX_54063324_54188254 | FAM120C | chrX | 54063324 | 54188254 |
g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM120C_chrX_54063324_54188254 | FAM120C | chrX | 54063324 | 54188254 |
g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM120C_chrX_54063324_54188254 | FAM120C | chrX | 54063324 | 54188254 |
g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM120C_chrX_54063324_54188254 | FAM120C | chrX | 54063324 | 54188254 |
g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM120C_chrX_54063324_54188254 | FAM120C | chrX | 54063324 | 54188254 |
g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM120C_chrX_54063324_54188254 | FAM120C | chrX | 54063324 | 54188254 |
g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM120C_chrX_54063324_54188254 | FAM120C | chrX | 54063324 | 54188254 |
g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM120C_chrX_54063324_54188254 | FAM120C | chrX | 54063324 | 54188254 |
g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM120C_chrX_54063324_54188254 | FAM120C | chrX | 54063324 | 54188254 |
g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM120C_chrX_54063324_54188254 | FAM120C | chrX | 54063324 | 54188254 |
g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM120C_chrX_54063324_54188254 | FAM120C | chrX | 54063324 | 54188254 |
g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM120C_chrX_54063324_54188254 | FAM120C | chrX | 54063324 | 54188254 |
g0066 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM120C_chrX_54063324_54188254 | FAM120C | chrX | 54063324 | 54188254 |
g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM120C_chrX_54063324_54188254 | FAM120C | chrX | 54063324 | 54188254 |
g0068 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM120C_chrX_54063324_54188254 | FAM120C | chrX | 54063324 | 54188254 |
g0069 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM120C_chrX_54063324_54188254 | FAM120C | chrX | 54063324 | 54188254 |
g0070 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM120C_chrX_54063324_54188254 | FAM120C | chrX | 54063324 | 54188254 |
g0071 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM120C_chrX_54063324_54188254 | FAM120C | chrX | 54063324 | 54188254 |
g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM120C_chrX_54063324_54188254 | FAM120C | chrX | 54063324 | 54188254 |
g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM120C_chrX_54063324_54188254 | FAM120C | chrX | 54063324 | 54188254 |
g0074 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM120C_chrX_54063324_54188254 | FAM120C | chrX | 54063324 | 54188254 |
g0075 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM120C_chrX_54063324_54188254 | FAM120C | chrX | 54063324 | 54188254 |
g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM120C_chrX_54063324_54188254 | FAM120C | chrX | 54063324 | 54188254 |
g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM120C_chrX_54063324_54188254 | FAM120C | chrX | 54063324 | 54188254 |
g0078 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM120C_chrX_54063324_54188254 | FAM120C | chrX | 54063324 | 54188254 |
g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM120C_chrX_54063324_54188254 | FAM120C | chrX | 54063324 | 54188254 |
g0080 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM120C_chrX_54063324_54188254 | FAM120C | chrX | 54063324 | 54188254 |
g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM120C_chrX_54063324_54188254 | FAM120C | chrX | 54063324 | 54188254 |
g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM120C_chrX_54063324_54188254 | FAM120C | chrX | 54063324 | 54188254 |
g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM120C_chrX_54063324_54188254 | FAM120C | chrX | 54063324 | 54188254 |
g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM120C_chrX_54063324_54188254 | FAM120C | chrX | 54063324 | 54188254 |
g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM120C_chrX_54063324_54188254 | FAM120C | chrX | 54063324 | 54188254 |
g0086 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM120C_chrX_54063324_54188254 | FAM120C | chrX | 54063324 | 54188254 |
g0087 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM120C_chrX_54063324_54188254 | FAM120C | chrX | 54063324 | 54188254 |
g0088 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM120C_chrX_54063324_54188254 | FAM120C | chrX | 54063324 | 54188254 |
g0089 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM120C_chrX_54063324_54188254 | FAM120C | chrX | 54063324 | 54188254 |
g0090 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM120C_chrX_54063324_54188254 | FAM120C | chrX | 54063324 | 54188254 |
g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM120C_chrX_54063324_54188254 | FAM120C | chrX | 54063324 | 54188254 |
g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM120C_chrX_54063324_54188254 | FAM120C | chrX | 54063324 | 54188254 |
g0093 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM120C_chrX_54063324_54188254 | FAM120C | chrX | 54063324 | 54188254 |
g0094 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM120C_chrX_54063324_54188254 | FAM120C | chrX | 54063324 | 54188254 |
g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM120C_chrX_54063324_54188254 | FAM120C | chrX | 54063324 | 54188254 |
g0096 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM120C_chrX_54063324_54188254 | FAM120C | chrX | 54063324 | 54188254 |
g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM120C_chrX_54063324_54188254 | FAM120C | chrX | 54063324 | 54188254 |
g0098 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM120C_chrX_54063324_54188254 | FAM120C | chrX | 54063324 | 54188254 |
g0099 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM120C_chrX_54063324_54188254 | FAM120C | chrX | 54063324 | 54188254 |
g0100 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM120C_chrX_54063324_54188254 | FAM120C | chrX | 54063324 | 54188254 |
g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM120C_chrX_54063324_54188254 | FAM120C | chrX | 54063324 | 54188254 |
g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM120C_chrX_54063324_54188254 | FAM120C | chrX | 54063324 | 54188254 |
g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM120C_chrX_54063324_54188254 | FAM120C | chrX | 54063324 | 54188254 |
g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM120C_chrX_54063324_54188254 | FAM120C | chrX | 54063324 | 54188254 |
g0105 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM120C_chrX_54063324_54188254 | FAM120C | chrX | 54063324 | 54188254 |
g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM120C_chrX_54063324_54188254 | FAM120C | chrX | 54063324 | 54188254 |
g0107 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM120C_chrX_54063324_54188254 | FAM120C | chrX | 54063324 | 54188254 |
g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM120C_chrX_54063324_54188254 | FAM120C | chrX | 54063324 | 54188254 |
g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM120C_chrX_54063324_54188254 | FAM120C | chrX | 54063324 | 54188254 |
g0110 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM120C_chrX_54063324_54188254 | FAM120C | chrX | 54063324 | 54188254 |
g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM120C_chrX_54063324_54188254 | FAM120C | chrX | 54063324 | 54188254 |
g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM120C_chrX_54063324_54188254 | FAM120C | chrX | 54063324 | 54188254 |
g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM120C_chrX_54063324_54188254 | FAM120C | chrX | 54063324 | 54188254 |
g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM120C_chrX_54063324_54188254 | FAM120C | chrX | 54063324 | 54188254 |
g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM120C_chrX_54063324_54188254 | FAM120C | chrX | 54063324 | 54188254 |
g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM120C_chrX_54063324_54188254 | FAM120C | chrX | 54063324 | 54188254 |
g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM120C_chrX_54063324_54188254 | FAM120C | chrX | 54063324 | 54188254 |
g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM120C_chrX_54063324_54188254 | FAM120C | chrX | 54063324 | 54188254 |
g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM120C_chrX_54063324_54188254 | FAM120C | chrX | 54063324 | 54188254 |
g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM120C_chrX_54063324_54188254 | FAM120C | chrX | 54063324 | 54188254 |
g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM120C_chrX_54063324_54188254 | FAM120C | chrX | 54063324 | 54188254 |
g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM120C_chrX_54063324_54188254 | FAM120C | chrX | 54063324 | 54188254 |
g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM120C_chrX_54063324_54188254 | FAM120C | chrX | 54063324 | 54188254 |
g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM120C_chrX_54063324_54188254 | FAM120C | chrX | 54063324 | 54188254 |
g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM120C_chrX_54063324_54188254 | FAM120C | chrX | 54063324 | 54188254 |
g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM120C_chrX_54063324_54188254 | FAM120C | chrX | 54063324 | 54188254 |
g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM120C_chrX_54063324_54188254 | FAM120C | chrX | 54063324 | 54188254 |
g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM120C_chrX_54063324_54188254 | FAM120C | chrX | 54063324 | 54188254 |
g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM120C_chrX_54063324_54188254 | FAM120C | chrX | 54063324 | 54188254 |
g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM120C_chrX_54063324_54188254 | FAM120C | chrX | 54063324 | 54188254 |
g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM120C_chrX_54063324_54188254 | FAM120C | chrX | 54063324 | 54188254 |
g0132 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM120C_chrX_54063324_54188254 | FAM120C | chrX | 54063324 | 54188254 |
g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM120C_chrX_54063324_54188254 | FAM120C | chrX | 54063324 | 54188254 |
g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM120C_chrX_54063324_54188254 | FAM120C | chrX | 54063324 | 54188254 |
g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM120C_chrX_54063324_54188254 | FAM120C | chrX | 54063324 | 54188254 |
g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM120C_chrX_54063324_54188254 | FAM120C | chrX | 54063324 | 54188254 |
g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM120C_chrX_54063324_54188254 | FAM120C | chrX | 54063324 | 54188254 |
g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM120C_chrX_54063324_54188254 | FAM120C | chrX | 54063324 | 54188254 |
g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM120C_chrX_54063324_54188254 | FAM120C | chrX | 54063324 | 54188254 |
g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM120C_chrX_54063324_54188254 | FAM120C | chrX | 54063324 | 54188254 |
g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM120C_chrX_54063324_54188254 | FAM120C | chrX | 54063324 | 54188254 |
g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM120C_chrX_54063324_54188254 | FAM120C | chrX | 54063324 | 54188254 |
g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM120C_chrX_54063324_54188254 | FAM120C | chrX | 54063324 | 54188254 |
g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM120C_chrX_54063324_54188254 | FAM120C | chrX | 54063324 | 54188254 |
g0145 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM120C_chrX_54063324_54188254 | FAM120C | chrX | 54063324 | 54188254 |
g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM120C_chrX_54063324_54188254 | FAM120C | chrX | 54063324 | 54188254 |
g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM120C_chrX_54063324_54188254 | FAM120C | chrX | 54063324 | 54188254 |
g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM120C_chrX_54063324_54188254 | FAM120C | chrX | 54063324 | 54188254 |
g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM120C_chrX_54063324_54188254 | FAM120C | chrX | 54063324 | 54188254 |
g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM120C_chrX_54063324_54188254 | FAM120C | chrX | 54063324 | 54188254 |
g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM120C_chrX_54063324_54188254 | FAM120C | chrX | 54063324 | 54188254 |
g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM120C_chrX_54063324_54188254 | FAM120C | chrX | 54063324 | 54188254 |
g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM120C_chrX_54063324_54188254 | FAM120C | chrX | 54063324 | 54188254 |
g0154 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM120C_chrX_54063324_54188254 | FAM120C | chrX | 54063324 | 54188254 |
g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM120C_chrX_54063324_54188254 | FAM120C | chrX | 54063324 | 54188254 |
g0156 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM120C_chrX_54063324_54188254 | FAM120C | chrX | 54063324 | 54188254 |
g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM120C_chrX_54063324_54188254 | FAM120C | chrX | 54063324 | 54188254 |
g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM120C_chrX_54063324_54188254 | FAM120C | chrX | 54063324 | 54188254 |
g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM120C_chrX_54063324_54188254 | FAM120C | chrX | 54063324 | 54188254 |
g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM120C_chrX_54063324_54188254 | FAM120C | chrX | 54063324 | 54188254 |
g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM120C_chrX_54063324_54188254 | FAM120C | chrX | 54063324 | 54188254 |
g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM120C_chrX_54063324_54188254 | FAM120C | chrX | 54063324 | 54188254 |
g0163 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM120C_chrX_54063324_54188254 | FAM120C | chrX | 54063324 | 54188254 |
g0164 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM120C_chrX_54063324_54188254 | FAM120C | chrX | 54063324 | 54188254 |
g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM120C_chrX_54063324_54188254 | FAM120C | chrX | 54063324 | 54188254 |
g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM120C_chrX_54063324_54188254 | FAM120C | chrX | 54063324 | 54188254 |
g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM120C_chrX_54063324_54188254 | FAM120C | chrX | 54063324 | 54188254 |
g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM120C_chrX_54063324_54188254 | FAM120C | chrX | 54063324 | 54188254 |
g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM120C_chrX_54063324_54188254 | FAM120C | chrX | 54063324 | 54188254 |
g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM120C_chrX_54063324_54188254 | FAM120C | chrX | 54063324 | 54188254 |
g0171 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM120C_chrX_54063324_54188254 | FAM120C | chrX | 54063324 | 54188254 |
g0172 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | FAM120C_chrX_54063324_54188254 | FAM120C | chrX | 54063324 | 54188254 |
g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM120C_chrX_54063324_54188254 | FAM120C | chrX | 54063324 | 54188254 |
g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM120C_chrX_54063324_54188254 | FAM120C | chrX | 54063324 | 54188254 |
g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM120C_chrX_54063324_54188254 | FAM120C | chrX | 54063324 | 54188254 |
g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM120C_chrX_54063324_54188254 | FAM120C | chrX | 54063324 | 54188254 |
g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM120C_chrX_54063324_54188254 | FAM120C | chrX | 54063324 | 54188254 |
g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM120C_chrX_54063324_54188254 | FAM120C | chrX | 54063324 | 54188254 |
g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM120C_chrX_54063324_54188254 | FAM120C | chrX | 54063324 | 54188254 |
g0180 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM120C_chrX_54063324_54188254 | FAM120C | chrX | 54063324 | 54188254 |
g0181 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM120C_chrX_54063324_54188254 | FAM120C | chrX | 54063324 | 54188254 |
g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM120C_chrX_54063324_54188254 | FAM120C | chrX | 54063324 | 54188254 |
g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM120C_chrX_54063324_54188254 | FAM120C | chrX | 54063324 | 54188254 |
g0184 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM120C_chrX_54063324_54188254 | FAM120C | chrX | 54063324 | 54188254 |
g0185 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM120C_chrX_54063324_54188254 | FAM120C | chrX | 54063324 | 54188254 |
g0186 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM120C_chrX_54063324_54188254 | FAM120C | chrX | 54063324 | 54188254 |
g0187 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM120C_chrX_54063324_54188254 | FAM120C | chrX | 54063324 | 54188254 |
g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM120C_chrX_54063324_54188254 | FAM120C | chrX | 54063324 | 54188254 |
achapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 1/1 | 3291 | 177 | 47 | 28 | 81 | 3 | 16 | FAM120C_chrX_54063324_54188254 | FAM120C | copy fasta | chrX | 54063324 | 54188254 |
a0001c0005 | 0/0 | 3291 | 1 | 0 | 0 | 1 | 0 | 0 | FAM120C_chrX_54063324_54188254 | FAM120C | copy fasta | chrX | 54063324 | 54188254 |
a0001c0009 | 0/0 | 3291 | 1 | 0 | 0 | 1 | 0 | 0 | FAM120C_chrX_54063324_54188254 | FAM120C | copy fasta | chrX | 54063324 | 54188254 |
a0002c0002 | 0/0 | 3297 | 4 | 0 | 3 | 0 | 1 | 0 | FAM120C_chrX_54063324_54188254 | FAM120C | copy fasta | chrX | 54063324 | 54188254 |
a0003c0003 | 0/0 | 3291 | 2 | 2 | 0 | 0 | 0 | 0 | FAM120C_chrX_54063324_54188254 | FAM120C | copy fasta | chrX | 54063324 | 54188254 |
a0004c0008 | 0/0 | 3291 | 1 | 0 | 0 | 0 | 1 | 0 | FAM120C_chrX_54063324_54188254 | FAM120C | copy fasta | chrX | 54063324 | 54188254 |
a0005c0007 | 0/0 | 3288 | 1 | 0 | 0 | 1 | 0 | 0 | FAM120C_chrX_54063324_54188254 | FAM120C | copy fasta | chrX | 54063324 | 54188254 |
a0006c0006 | 0/0 | 3290 | 1 | 0 | 0 | 1 | 0 | 0 | FAM120C_chrX_54063324_54188254 | FAM120C | copy fasta | chrX | 54063324 | 54188254 |
a0007c0004 | 0/0 | 3291 | 1 | 1 | 0 | 0 | 0 | 0 | FAM120C_chrX_54063324_54188254 | FAM120C | copy fasta | chrX | 54063324 | 54188254 |
a0008c0010 | 0/0 | 3293 | 1 | 0 | 0 | 1 | 0 | 0 | FAM120C_chrX_54063324_54188254 | FAM120C | copy fasta | chrX | 54063324 | 54188254 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 0/0 | 8058 | 14 | 0 | 2 | 12 | 0 | 0 | FAM120C_chrX_54063324_54188254 | FAM120C | copy fasta | chrX | 54063324 | 54188254 |
a0001c0001t0002 | 0/1 | 8043 | 11 | 0 | 1 | 9 | 0 | 0 | FAM120C_chrX_54063324_54188254 | FAM120C | copy fasta | chrX | 54063324 | 54188254 |
a0001c0001t0003 | 0/0 | 8048 | 9 | 1 | 3 | 3 | 0 | 2 | FAM120C_chrX_54063324_54188254 | FAM120C | copy fasta | chrX | 54063324 | 54188254 |
a0001c0001t0004 | 0/0 | 8056 | 7 | 0 | 5 | 2 | 0 | 0 | FAM120C_chrX_54063324_54188254 | FAM120C | copy fasta | chrX | 54063324 | 54188254 |
a0001c0001t0005 | 0/0 | 8060 | 7 | 0 | 0 | 7 | 0 | 0 | FAM120C_chrX_54063324_54188254 | FAM120C | copy fasta | chrX | 54063324 | 54188254 |
a0001c0001t0006 | 0/0 | 8044 | 5 | 0 | 0 | 5 | 0 | 0 | FAM120C_chrX_54063324_54188254 | FAM120C | copy fasta | chrX | 54063324 | 54188254 |
a0001c0001t0007 | 0/0 | 8059 | 5 | 0 | 0 | 5 | 0 | 0 | FAM120C_chrX_54063324_54188254 | FAM120C | copy fasta | chrX | 54063324 | 54188254 |
a0001c0001t0008 | 0/0 | 8041 | 6 | 2 | 0 | 4 | 0 | 0 | FAM120C_chrX_54063324_54188254 | FAM120C | copy fasta | chrX | 54063324 | 54188254 |
a0001c0001t0009 | 0/0 | 8063 | 5 | 0 | 1 | 3 | 0 | 1 | FAM120C_chrX_54063324_54188254 | FAM120C | copy fasta | chrX | 54063324 | 54188254 |
a0001c0001t0010 | 0/0 | 8062 | 6 | 0 | 0 | 6 | 0 | 0 | FAM120C_chrX_54063324_54188254 | FAM120C | copy fasta | chrX | 54063324 | 54188254 |
a0001c0001t0011 | 0/0 | 8046 | 5 | 1 | 2 | 2 | 0 | 0 | FAM120C_chrX_54063324_54188254 | FAM120C | copy fasta | chrX | 54063324 | 54188254 |
a0001c0001t0012 | 0/0 | 8046 | 5 | 0 | 0 | 2 | 0 | 3 | FAM120C_chrX_54063324_54188254 | FAM120C | copy fasta | chrX | 54063324 | 54188254 |
a0001c0001t0013 | 0/0 | 8064 | 2 | 2 | 0 | 0 | 0 | 0 | FAM120C_chrX_54063324_54188254 | FAM120C | copy fasta | chrX | 54063324 | 54188254 |
a0001c0001t0014 | 0/0 | 8044 | 4 | 0 | 1 | 0 | 0 | 3 | FAM120C_chrX_54063324_54188254 | FAM120C | copy fasta | chrX | 54063324 | 54188254 |
a0001c0001t0015 | 0/0 | 8066 | 4 | 4 | 0 | 0 | 0 | 0 | FAM120C_chrX_54063324_54188254 | FAM120C | copy fasta | chrX | 54063324 | 54188254 |
a0001c0001t0016 | 0/0 | 8053 | 4 | 4 | 0 | 0 | 0 | 0 | FAM120C_chrX_54063324_54188254 | FAM120C | copy fasta | chrX | 54063324 | 54188254 |
a0001c0001t0017 | 0/0 | 8045 | 4 | 1 | 3 | 0 | 0 | 0 | FAM120C_chrX_54063324_54188254 | FAM120C | copy fasta | chrX | 54063324 | 54188254 |
a0001c0001t0018 | 0/0 | 8056 | 3 | 3 | 0 | 0 | 0 | 0 | FAM120C_chrX_54063324_54188254 | FAM120C | copy fasta | chrX | 54063324 | 54188254 |
a0001c0001t0019 | 0/0 | 8059 | 2 | 2 | 0 | 0 | 0 | 0 | FAM120C_chrX_54063324_54188254 | FAM120C | copy fasta | chrX | 54063324 | 54188254 |
a0001c0001t0020 | 0/0 | 8039 | 3 | 2 | 1 | 0 | 0 | 0 | FAM120C_chrX_54063324_54188254 | FAM120C | copy fasta | chrX | 54063324 | 54188254 |
a0001c0001t0021 | 0/0 | 8054 | 3 | 0 | 0 | 3 | 0 | 0 | FAM120C_chrX_54063324_54188254 | FAM120C | copy fasta | chrX | 54063324 | 54188254 |
a0001c0001t0022 | 0/0 | 8071 | 3 | 3 | 0 | 0 | 0 | 0 | FAM120C_chrX_54063324_54188254 | FAM120C | copy fasta | chrX | 54063324 | 54188254 |
a0001c0001t0023 | 0/0 | 8053 | 3 | 0 | 1 | 1 | 1 | 0 | FAM120C_chrX_54063324_54188254 | FAM120C | copy fasta | chrX | 54063324 | 54188254 |
a0001c0001t0024 | 0/0 | 8052 | 2 | 0 | 0 | 1 | 0 | 1 | FAM120C_chrX_54063324_54188254 | FAM120C | copy fasta | chrX | 54063324 | 54188254 |
a0001c0001t0025 | 0/0 | 8066 | 2 | 2 | 0 | 0 | 0 | 0 | FAM120C_chrX_54063324_54188254 | FAM120C | copy fasta | chrX | 54063324 | 54188254 |
a0001c0001t0026 | 0/0 | 8061 | 2 | 2 | 0 | 0 | 0 | 0 | FAM120C_chrX_54063324_54188254 | FAM120C | copy fasta | chrX | 54063324 | 54188254 |
a0001c0001t0027 | 0/0 | 8056 | 2 | 2 | 0 | 0 | 0 | 0 | FAM120C_chrX_54063324_54188254 | FAM120C | copy fasta | chrX | 54063324 | 54188254 |
a0001c0001t0028 | 0/0 | 8061 | 2 | 0 | 1 | 0 | 1 | 0 | FAM120C_chrX_54063324_54188254 | FAM120C | copy fasta | chrX | 54063324 | 54188254 |
a0001c0001t0029 | 0/0 | 8051 | 2 | 0 | 0 | 0 | 1 | 1 | FAM120C_chrX_54063324_54188254 | FAM120C | copy fasta | chrX | 54063324 | 54188254 |
a0001c0001t0030 | 0/0 | 8063 | 2 | 2 | 0 | 0 | 0 | 0 | FAM120C_chrX_54063324_54188254 | FAM120C | copy fasta | chrX | 54063324 | 54188254 |
a0001c0001t0031 | 0/0 | 8058 | 2 | 1 | 1 | 0 | 0 | 0 | FAM120C_chrX_54063324_54188254 | FAM120C | copy fasta | chrX | 54063324 | 54188254 |
a0001c0001t0032 | 0/0 | 8038 | 2 | 0 | 0 | 2 | 0 | 0 | FAM120C_chrX_54063324_54188254 | FAM120C | copy fasta | chrX | 54063324 | 54188254 |
a0001c0001t0033 | 0/0 | 8071 | 2 | 2 | 0 | 0 | 0 | 0 | FAM120C_chrX_54063324_54188254 | FAM120C | copy fasta | chrX | 54063324 | 54188254 |
a0001c0001t0035 | 0/0 | 8053 | 1 | 0 | 0 | 1 | 0 | 0 | FAM120C_chrX_54063324_54188254 | FAM120C | copy fasta | chrX | 54063324 | 54188254 |
a0001c0001t0036 | 0/0 | 8050 | 1 | 0 | 1 | 0 | 0 | 0 | FAM120C_chrX_54063324_54188254 | FAM120C | copy fasta | chrX | 54063324 | 54188254 |
a0001c0001t0037 | 0/0 | 8044 | 1 | 0 | 0 | 1 | 0 | 0 | FAM120C_chrX_54063324_54188254 | FAM120C | copy fasta | chrX | 54063324 | 54188254 |
a0001c0001t0038 | 0/0 | 8046 | 1 | 0 | 0 | 0 | 0 | 1 | FAM120C_chrX_54063324_54188254 | FAM120C | copy fasta | chrX | 54063324 | 54188254 |
a0001c0001t0039 | 0/0 | 8058 | 1 | 1 | 0 | 0 | 0 | 0 | FAM120C_chrX_54063324_54188254 | FAM120C | copy fasta | chrX | 54063324 | 54188254 |
a0001c0001t0040 | 1/0 | 8056 | 1 | 0 | 0 | 0 | 0 | 0 | FAM120C_chrX_54063324_54188254 | FAM120C | copy fasta | chrX | 54063324 | 54188254 |
a0001c0001t0041 | 0/0 | 8067 | 1 | 0 | 1 | 0 | 0 | 0 | FAM120C_chrX_54063324_54188254 | FAM120C | copy fasta | chrX | 54063324 | 54188254 |
a0001c0001t0042 | 0/0 | 8057 | 1 | 1 | 0 | 0 | 0 | 0 | FAM120C_chrX_54063324_54188254 | FAM120C | copy fasta | chrX | 54063324 | 54188254 |
a0001c0001t0043 | 0/0 | 8042 | 1 | 1 | 0 | 0 | 0 | 0 | FAM120C_chrX_54063324_54188254 | FAM120C | copy fasta | chrX | 54063324 | 54188254 |
a0001c0001t0044 | 0/0 | 8037 | 1 | 0 | 0 | 0 | 0 | 1 | FAM120C_chrX_54063324_54188254 | FAM120C | copy fasta | chrX | 54063324 | 54188254 |
a0001c0001t0045 | 0/0 | 8042 | 1 | 1 | 0 | 0 | 0 | 0 | FAM120C_chrX_54063324_54188254 | FAM120C | copy fasta | chrX | 54063324 | 54188254 |
a0001c0001t0046 | 0/0 | 8064 | 1 | 0 | 0 | 1 | 0 | 0 | FAM120C_chrX_54063324_54188254 | FAM120C | copy fasta | chrX | 54063324 | 54188254 |
a0001c0001t0048 | 0/0 | 8051 | 1 | 1 | 0 | 0 | 0 | 0 | FAM120C_chrX_54063324_54188254 | FAM120C | copy fasta | chrX | 54063324 | 54188254 |
a0001c0001t0049 | 0/0 | 8051 | 1 | 1 | 0 | 0 | 0 | 0 | FAM120C_chrX_54063324_54188254 | FAM120C | copy fasta | chrX | 54063324 | 54188254 |
a0001c0001t0050 | 0/0 | 8046 | 1 | 0 | 0 | 1 | 0 | 0 | FAM120C_chrX_54063324_54188254 | FAM120C | copy fasta | chrX | 54063324 | 54188254 |
a0001c0001t0052 | 0/0 | 8061 | 1 | 0 | 1 | 0 | 0 | 0 | FAM120C_chrX_54063324_54188254 | FAM120C | copy fasta | chrX | 54063324 | 54188254 |
a0001c0001t0053 | 0/0 | 8058 | 1 | 0 | 1 | 0 | 0 | 0 | FAM120C_chrX_54063324_54188254 | FAM120C | copy fasta | chrX | 54063324 | 54188254 |
a0001c0001t0054 | 0/0 | 8068 | 1 | 1 | 0 | 0 | 0 | 0 | FAM120C_chrX_54063324_54188254 | FAM120C | copy fasta | chrX | 54063324 | 54188254 |
a0001c0001t0055 | 0/0 | 8068 | 1 | 0 | 0 | 1 | 0 | 0 | FAM120C_chrX_54063324_54188254 | FAM120C | copy fasta | chrX | 54063324 | 54188254 |
a0001c0001t0056 | 0/0 | 8058 | 1 | 1 | 0 | 0 | 0 | 0 | FAM120C_chrX_54063324_54188254 | FAM120C | copy fasta | chrX | 54063324 | 54188254 |
a0001c0001t0057 | 0/0 | 8048 | 1 | 0 | 0 | 1 | 0 | 0 | FAM120C_chrX_54063324_54188254 | FAM120C | copy fasta | chrX | 54063324 | 54188254 |
a0001c0001t0058 | 0/0 | 8063 | 1 | 0 | 1 | 0 | 0 | 0 | FAM120C_chrX_54063324_54188254 | FAM120C | copy fasta | chrX | 54063324 | 54188254 |
a0001c0001t0059 | 0/0 | 8058 | 1 | 0 | 0 | 0 | 0 | 1 | FAM120C_chrX_54063324_54188254 | FAM120C | copy fasta | chrX | 54063324 | 54188254 |
a0001c0001t0060 | 0/0 | 8070 | 1 | 1 | 0 | 0 | 0 | 0 | FAM120C_chrX_54063324_54188254 | FAM120C | copy fasta | chrX | 54063324 | 54188254 |
a0001c0001t0061 | 0/0 | 8065 | 1 | 0 | 1 | 0 | 0 | 0 | FAM120C_chrX_54063324_54188254 | FAM120C | copy fasta | chrX | 54063324 | 54188254 |
a0001c0001t0062 | 0/0 | 8055 | 1 | 0 | 0 | 1 | 0 | 0 | FAM120C_chrX_54063324_54188254 | FAM120C | copy fasta | chrX | 54063324 | 54188254 |
a0001c0001t0063 | 0/0 | 8050 | 1 | 0 | 0 | 1 | 0 | 0 | FAM120C_chrX_54063324_54188254 | FAM120C | copy fasta | chrX | 54063324 | 54188254 |
a0001c0001t0064 | 0/0 | 8065 | 1 | 0 | 0 | 1 | 0 | 0 | FAM120C_chrX_54063324_54188254 | FAM120C | copy fasta | chrX | 54063324 | 54188254 |
a0001c0001t0065 | 0/0 | 8067 | 1 | 0 | 0 | 1 | 0 | 0 | FAM120C_chrX_54063324_54188254 | FAM120C | copy fasta | chrX | 54063324 | 54188254 |
a0001c0001t0066 | 0/0 | 8052 | 1 | 0 | 0 | 1 | 0 | 0 | FAM120C_chrX_54063324_54188254 | FAM120C | copy fasta | chrX | 54063324 | 54188254 |
a0001c0001t0067 | 0/0 | 8064 | 1 | 1 | 0 | 0 | 0 | 0 | FAM120C_chrX_54063324_54188254 | FAM120C | copy fasta | chrX | 54063324 | 54188254 |
a0001c0001t0068 | 0/0 | 8054 | 1 | 0 | 0 | 0 | 0 | 1 | FAM120C_chrX_54063324_54188254 | FAM120C | copy fasta | chrX | 54063324 | 54188254 |
a0001c0001t0069 | 0/0 | 8058 | 1 | 0 | 0 | 0 | 0 | 1 | FAM120C_chrX_54063324_54188254 | FAM120C | copy fasta | chrX | 54063324 | 54188254 |
a0001c0001t0070 | 0/0 | 8053 | 1 | 0 | 0 | 1 | 0 | 0 | FAM120C_chrX_54063324_54188254 | FAM120C | copy fasta | chrX | 54063324 | 54188254 |
a0001c0001t0072 | 0/0 | 8059 | 1 | 1 | 0 | 0 | 0 | 0 | FAM120C_chrX_54063324_54188254 | FAM120C | copy fasta | chrX | 54063324 | 54188254 |
a0001c0001t0073 | 0/0 | 8047 | 1 | 0 | 0 | 1 | 0 | 0 | FAM120C_chrX_54063324_54188254 | FAM120C | copy fasta | chrX | 54063324 | 54188254 |
a0001c0001t0074 | 0/0 | 8045 | 1 | 0 | 0 | 1 | 0 | 0 | FAM120C_chrX_54063324_54188254 | FAM120C | copy fasta | chrX | 54063324 | 54188254 |
a0001c0005t0006 | 0/0 | 8044 | 1 | 0 | 0 | 1 | 0 | 0 | FAM120C_chrX_54063324_54188254 | FAM120C | copy fasta | chrX | 54063324 | 54188254 |
a0001c0009t0071 | 0/0 | 8045 | 1 | 0 | 0 | 1 | 0 | 0 | FAM120C_chrX_54063324_54188254 | FAM120C | copy fasta | chrX | 54063324 | 54188254 |
a0002c0002t0001 | 0/0 | 8064 | 1 | 0 | 0 | 0 | 1 | 0 | FAM120C_chrX_54063324_54188254 | FAM120C | copy fasta | chrX | 54063324 | 54188254 |
a0002c0002t0007 | 0/0 | 8065 | 1 | 0 | 1 | 0 | 0 | 0 | FAM120C_chrX_54063324_54188254 | FAM120C | copy fasta | chrX | 54063324 | 54188254 |
a0002c0002t0019 | 0/0 | 8065 | 1 | 0 | 1 | 0 | 0 | 0 | FAM120C_chrX_54063324_54188254 | FAM120C | copy fasta | chrX | 54063324 | 54188254 |
a0002c0002t0047 | 0/0 | 8057 | 1 | 0 | 1 | 0 | 0 | 0 | FAM120C_chrX_54063324_54188254 | FAM120C | copy fasta | chrX | 54063324 | 54188254 |
a0003c0003t0013 | 0/0 | 8064 | 2 | 2 | 0 | 0 | 0 | 0 | FAM120C_chrX_54063324_54188254 | FAM120C | copy fasta | chrX | 54063324 | 54188254 |
a0004c0008t0009 | 0/0 | 8063 | 1 | 0 | 0 | 0 | 1 | 0 | FAM120C_chrX_54063324_54188254 | FAM120C | copy fasta | chrX | 54063324 | 54188254 |
a0005c0007t0034 | 0/0 | 8063 | 1 | 0 | 0 | 1 | 0 | 0 | FAM120C_chrX_54063324_54188254 | FAM120C | copy fasta | chrX | 54063324 | 54188254 |
a0006c0006t0001 | 0/0 | 8057 | 1 | 0 | 0 | 1 | 0 | 0 | FAM120C_chrX_54063324_54188254 | FAM120C | copy fasta | chrX | 54063324 | 54188254 |
a0007c0004t0051 | 0/0 | 8031 | 1 | 1 | 0 | 0 | 0 | 0 | FAM120C_chrX_54063324_54188254 | FAM120C | copy fasta | chrX | 54063324 | 54188254 |
a0008c0010t0075 | 0/0 | 8048 | 1 | 0 | 0 | 1 | 0 | 0 | FAM120C_chrX_54063324_54188254 | FAM120C | copy fasta | chrX | 54063324 | 54188254 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0001 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | FAM120C_chrX_54063324_54188254 | FAM120C | chrX | 54063324 | 54188254 |
a0001c0001t0001g0008 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM120C_chrX_54063324_54188254 | FAM120C | chrX | 54063324 | 54188254 |
a0001c0001t0001g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM120C_chrX_54063324_54188254 | FAM120C | chrX | 54063324 | 54188254 |
a0001c0001t0001g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM120C_chrX_54063324_54188254 | FAM120C | chrX | 54063324 | 54188254 |
a0001c0001t0001g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM120C_chrX_54063324_54188254 | FAM120C | chrX | 54063324 | 54188254 |
a0001c0001t0001g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM120C_chrX_54063324_54188254 | FAM120C | chrX | 54063324 | 54188254 |
a0001c0001t0001g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM120C_chrX_54063324_54188254 | FAM120C | chrX | 54063324 | 54188254 |
a0001c0001t0001g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM120C_chrX_54063324_54188254 | FAM120C | chrX | 54063324 | 54188254 |
a0001c0001t0001g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM120C_chrX_54063324_54188254 | FAM120C | chrX | 54063324 | 54188254 |
a0001c0001t0001g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM120C_chrX_54063324_54188254 | FAM120C | chrX | 54063324 | 54188254 |
a0001c0001t0001g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM120C_chrX_54063324_54188254 | FAM120C | chrX | 54063324 | 54188254 |
a0001c0001t0001g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM120C_chrX_54063324_54188254 | FAM120C | chrX | 54063324 | 54188254 |
a0001c0001t0001g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM120C_chrX_54063324_54188254 | FAM120C | chrX | 54063324 | 54188254 |
a0001c0001t0002g0132 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM120C_chrX_54063324_54188254 | FAM120C | chrX | 54063324 | 54188254 |
a0001c0001t0002g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM120C_chrX_54063324_54188254 | FAM120C | chrX | 54063324 | 54188254 |
a0001c0001t0002g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM120C_chrX_54063324_54188254 | FAM120C | chrX | 54063324 | 54188254 |
a0001c0001t0002g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM120C_chrX_54063324_54188254 | FAM120C | chrX | 54063324 | 54188254 |
a0001c0001t0002g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM120C_chrX_54063324_54188254 | FAM120C | chrX | 54063324 | 54188254 |
a0001c0001t0002g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM120C_chrX_54063324_54188254 | FAM120C | chrX | 54063324 | 54188254 |
a0001c0001t0002g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM120C_chrX_54063324_54188254 | FAM120C | chrX | 54063324 | 54188254 |
a0001c0001t0002g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM120C_chrX_54063324_54188254 | FAM120C | chrX | 54063324 | 54188254 |
a0001c0001t0002g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM120C_chrX_54063324_54188254 | FAM120C | chrX | 54063324 | 54188254 |
a0001c0001t0002g0172 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | FAM120C_chrX_54063324_54188254 | FAM120C | chrX | 54063324 | 54188254 |
a0001c0001t0002g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM120C_chrX_54063324_54188254 | FAM120C | chrX | 54063324 | 54188254 |
a0001c0001t0003g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM120C_chrX_54063324_54188254 | FAM120C | chrX | 54063324 | 54188254 |
a0001c0001t0003g0038 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM120C_chrX_54063324_54188254 | FAM120C | chrX | 54063324 | 54188254 |
a0001c0001t0003g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM120C_chrX_54063324_54188254 | FAM120C | chrX | 54063324 | 54188254 |
a0001c0001t0003g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM120C_chrX_54063324_54188254 | FAM120C | chrX | 54063324 | 54188254 |
a0001c0001t0003g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM120C_chrX_54063324_54188254 | FAM120C | chrX | 54063324 | 54188254 |
a0001c0001t0003g0087 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM120C_chrX_54063324_54188254 | FAM120C | chrX | 54063324 | 54188254 |
a0001c0001t0003g0107 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM120C_chrX_54063324_54188254 | FAM120C | chrX | 54063324 | 54188254 |
a0001c0001t0003g0110 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM120C_chrX_54063324_54188254 | FAM120C | chrX | 54063324 | 54188254 |
a0001c0001t0003g0181 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM120C_chrX_54063324_54188254 | FAM120C | chrX | 54063324 | 54188254 |
a0001c0001t0004g0006 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM120C_chrX_54063324_54188254 | FAM120C | chrX | 54063324 | 54188254 |
a0001c0001t0004g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM120C_chrX_54063324_54188254 | FAM120C | chrX | 54063324 | 54188254 |
a0001c0001t0004g0045 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM120C_chrX_54063324_54188254 | FAM120C | chrX | 54063324 | 54188254 |
a0001c0001t0004g0069 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM120C_chrX_54063324_54188254 | FAM120C | chrX | 54063324 | 54188254 |
a0001c0001t0004g0071 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM120C_chrX_54063324_54188254 | FAM120C | chrX | 54063324 | 54188254 |
a0001c0001t0004g0086 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM120C_chrX_54063324_54188254 | FAM120C | chrX | 54063324 | 54188254 |
a0001c0001t0004g0180 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM120C_chrX_54063324_54188254 | FAM120C | chrX | 54063324 | 54188254 |
a0001c0001t0005g0011 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM120C_chrX_54063324_54188254 | FAM120C | chrX | 54063324 | 54188254 |
a0001c0001t0005g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM120C_chrX_54063324_54188254 | FAM120C | chrX | 54063324 | 54188254 |
a0001c0001t0005g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM120C_chrX_54063324_54188254 | FAM120C | chrX | 54063324 | 54188254 |
a0001c0001t0005g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM120C_chrX_54063324_54188254 | FAM120C | chrX | 54063324 | 54188254 |
a0001c0001t0005g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM120C_chrX_54063324_54188254 | FAM120C | chrX | 54063324 | 54188254 |
a0001c0001t0005g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM120C_chrX_54063324_54188254 | FAM120C | chrX | 54063324 | 54188254 |
a0001c0001t0005g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM120C_chrX_54063324_54188254 | FAM120C | chrX | 54063324 | 54188254 |
a0001c0001t0006g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM120C_chrX_54063324_54188254 | FAM120C | chrX | 54063324 | 54188254 |
a0001c0001t0006g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM120C_chrX_54063324_54188254 | FAM120C | chrX | 54063324 | 54188254 |
a0001c0001t0006g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM120C_chrX_54063324_54188254 | FAM120C | chrX | 54063324 | 54188254 |
a0001c0001t0006g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM120C_chrX_54063324_54188254 | FAM120C | chrX | 54063324 | 54188254 |
a0001c0001t0006g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM120C_chrX_54063324_54188254 | FAM120C | chrX | 54063324 | 54188254 |
a0001c0001t0007g0017 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM120C_chrX_54063324_54188254 | FAM120C | chrX | 54063324 | 54188254 |
a0001c0001t0007g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM120C_chrX_54063324_54188254 | FAM120C | chrX | 54063324 | 54188254 |
a0001c0001t0007g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM120C_chrX_54063324_54188254 | FAM120C | chrX | 54063324 | 54188254 |
a0001c0001t0007g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM120C_chrX_54063324_54188254 | FAM120C | chrX | 54063324 | 54188254 |
a0001c0001t0007g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM120C_chrX_54063324_54188254 | FAM120C | chrX | 54063324 | 54188254 |
a0001c0001t0008g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM120C_chrX_54063324_54188254 | FAM120C | chrX | 54063324 | 54188254 |
a0001c0001t0008g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM120C_chrX_54063324_54188254 | FAM120C | chrX | 54063324 | 54188254 |
a0001c0001t0008g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM120C_chrX_54063324_54188254 | FAM120C | chrX | 54063324 | 54188254 |
a0001c0001t0008g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM120C_chrX_54063324_54188254 | FAM120C | chrX | 54063324 | 54188254 |
a0001c0001t0008g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM120C_chrX_54063324_54188254 | FAM120C | chrX | 54063324 | 54188254 |
a0001c0001t0008g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM120C_chrX_54063324_54188254 | FAM120C | chrX | 54063324 | 54188254 |
a0001c0001t0009g0033 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM120C_chrX_54063324_54188254 | FAM120C | chrX | 54063324 | 54188254 |
a0001c0001t0009g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM120C_chrX_54063324_54188254 | FAM120C | chrX | 54063324 | 54188254 |
a0001c0001t0009g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM120C_chrX_54063324_54188254 | FAM120C | chrX | 54063324 | 54188254 |
a0001c0001t0009g0070 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM120C_chrX_54063324_54188254 | FAM120C | chrX | 54063324 | 54188254 |
a0001c0001t0009g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM120C_chrX_54063324_54188254 | FAM120C | chrX | 54063324 | 54188254 |
a0001c0001t0010g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM120C_chrX_54063324_54188254 | FAM120C | chrX | 54063324 | 54188254 |
a0001c0001t0010g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM120C_chrX_54063324_54188254 | FAM120C | chrX | 54063324 | 54188254 |
a0001c0001t0010g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM120C_chrX_54063324_54188254 | FAM120C | chrX | 54063324 | 54188254 |
a0001c0001t0010g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM120C_chrX_54063324_54188254 | FAM120C | chrX | 54063324 | 54188254 |
a0001c0001t0010g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM120C_chrX_54063324_54188254 | FAM120C | chrX | 54063324 | 54188254 |
a0001c0001t0010g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM120C_chrX_54063324_54188254 | FAM120C | chrX | 54063324 | 54188254 |
a0001c0001t0011g0010 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM120C_chrX_54063324_54188254 | FAM120C | chrX | 54063324 | 54188254 |
a0001c0001t0011g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM120C_chrX_54063324_54188254 | FAM120C | chrX | 54063324 | 54188254 |
a0001c0001t0011g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM120C_chrX_54063324_54188254 | FAM120C | chrX | 54063324 | 54188254 |
a0001c0001t0011g0163 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM120C_chrX_54063324_54188254 | FAM120C | chrX | 54063324 | 54188254 |
a0001c0001t0011g0164 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM120C_chrX_54063324_54188254 | FAM120C | chrX | 54063324 | 54188254 |
a0001c0001t0012g0035 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM120C_chrX_54063324_54188254 | FAM120C | chrX | 54063324 | 54188254 |
a0001c0001t0012g0043 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM120C_chrX_54063324_54188254 | FAM120C | chrX | 54063324 | 54188254 |
a0001c0001t0012g0047 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM120C_chrX_54063324_54188254 | FAM120C | chrX | 54063324 | 54188254 |
a0001c0001t0012g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM120C_chrX_54063324_54188254 | FAM120C | chrX | 54063324 | 54188254 |
a0001c0001t0012g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM120C_chrX_54063324_54188254 | FAM120C | chrX | 54063324 | 54188254 |
a0001c0001t0013g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM120C_chrX_54063324_54188254 | FAM120C | chrX | 54063324 | 54188254 |
a0001c0001t0013g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM120C_chrX_54063324_54188254 | FAM120C | chrX | 54063324 | 54188254 |
a0001c0001t0014g0046 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM120C_chrX_54063324_54188254 | FAM120C | chrX | 54063324 | 54188254 |
a0001c0001t0014g0075 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM120C_chrX_54063324_54188254 | FAM120C | chrX | 54063324 | 54188254 |
a0001c0001t0014g0093 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM120C_chrX_54063324_54188254 | FAM120C | chrX | 54063324 | 54188254 |
a0001c0001t0014g0094 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM120C_chrX_54063324_54188254 | FAM120C | chrX | 54063324 | 54188254 |
a0001c0001t0015g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM120C_chrX_54063324_54188254 | FAM120C | chrX | 54063324 | 54188254 |
a0001c0001t0015g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM120C_chrX_54063324_54188254 | FAM120C | chrX | 54063324 | 54188254 |
a0001c0001t0015g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM120C_chrX_54063324_54188254 | FAM120C | chrX | 54063324 | 54188254 |
a0001c0001t0015g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM120C_chrX_54063324_54188254 | FAM120C | chrX | 54063324 | 54188254 |
a0001c0001t0016g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM120C_chrX_54063324_54188254 | FAM120C | chrX | 54063324 | 54188254 |
a0001c0001t0016g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM120C_chrX_54063324_54188254 | FAM120C | chrX | 54063324 | 54188254 |
a0001c0001t0016g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM120C_chrX_54063324_54188254 | FAM120C | chrX | 54063324 | 54188254 |
a0001c0001t0016g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM120C_chrX_54063324_54188254 | FAM120C | chrX | 54063324 | 54188254 |
a0001c0001t0017g0005 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM120C_chrX_54063324_54188254 | FAM120C | chrX | 54063324 | 54188254 |
a0001c0001t0017g0154 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM120C_chrX_54063324_54188254 | FAM120C | chrX | 54063324 | 54188254 |
a0001c0001t0017g0171 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM120C_chrX_54063324_54188254 | FAM120C | chrX | 54063324 | 54188254 |
a0001c0001t0017g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM120C_chrX_54063324_54188254 | FAM120C | chrX | 54063324 | 54188254 |
a0001c0001t0018g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM120C_chrX_54063324_54188254 | FAM120C | chrX | 54063324 | 54188254 |
a0001c0001t0018g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM120C_chrX_54063324_54188254 | FAM120C | chrX | 54063324 | 54188254 |
a0001c0001t0018g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM120C_chrX_54063324_54188254 | FAM120C | chrX | 54063324 | 54188254 |
a0001c0001t0019g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM120C_chrX_54063324_54188254 | FAM120C | chrX | 54063324 | 54188254 |
a0001c0001t0019g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM120C_chrX_54063324_54188254 | FAM120C | chrX | 54063324 | 54188254 |
a0001c0001t0020g0002 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | FAM120C_chrX_54063324_54188254 | FAM120C | chrX | 54063324 | 54188254 |
a0001c0001t0020g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM120C_chrX_54063324_54188254 | FAM120C | chrX | 54063324 | 54188254 |
a0001c0001t0021g0014 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM120C_chrX_54063324_54188254 | FAM120C | chrX | 54063324 | 54188254 |
a0001c0001t0021g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM120C_chrX_54063324_54188254 | FAM120C | chrX | 54063324 | 54188254 |
a0001c0001t0021g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM120C_chrX_54063324_54188254 | FAM120C | chrX | 54063324 | 54188254 |
a0001c0001t0022g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM120C_chrX_54063324_54188254 | FAM120C | chrX | 54063324 | 54188254 |
a0001c0001t0022g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM120C_chrX_54063324_54188254 | FAM120C | chrX | 54063324 | 54188254 |
a0001c0001t0022g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM120C_chrX_54063324_54188254 | FAM120C | chrX | 54063324 | 54188254 |
a0001c0001t0023g0050 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM120C_chrX_54063324_54188254 | FAM120C | chrX | 54063324 | 54188254 |
a0001c0001t0023g0089 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM120C_chrX_54063324_54188254 | FAM120C | chrX | 54063324 | 54188254 |
a0001c0001t0023g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM120C_chrX_54063324_54188254 | FAM120C | chrX | 54063324 | 54188254 |
a0001c0001t0024g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM120C_chrX_54063324_54188254 | FAM120C | chrX | 54063324 | 54188254 |
a0001c0001t0024g0080 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM120C_chrX_54063324_54188254 | FAM120C | chrX | 54063324 | 54188254 |
a0001c0001t0025g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM120C_chrX_54063324_54188254 | FAM120C | chrX | 54063324 | 54188254 |
a0001c0001t0025g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM120C_chrX_54063324_54188254 | FAM120C | chrX | 54063324 | 54188254 |
a0001c0001t0026g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM120C_chrX_54063324_54188254 | FAM120C | chrX | 54063324 | 54188254 |
a0001c0001t0026g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM120C_chrX_54063324_54188254 | FAM120C | chrX | 54063324 | 54188254 |
a0001c0001t0027g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM120C_chrX_54063324_54188254 | FAM120C | chrX | 54063324 | 54188254 |
a0001c0001t0027g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM120C_chrX_54063324_54188254 | FAM120C | chrX | 54063324 | 54188254 |
a0001c0001t0028g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM120C_chrX_54063324_54188254 | FAM120C | chrX | 54063324 | 54188254 |
a0001c0001t0028g0066 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM120C_chrX_54063324_54188254 | FAM120C | chrX | 54063324 | 54188254 |
a0001c0001t0029g0068 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM120C_chrX_54063324_54188254 | FAM120C | chrX | 54063324 | 54188254 |
a0001c0001t0029g0088 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM120C_chrX_54063324_54188254 | FAM120C | chrX | 54063324 | 54188254 |
a0001c0001t0030g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM120C_chrX_54063324_54188254 | FAM120C | chrX | 54063324 | 54188254 |
a0001c0001t0030g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM120C_chrX_54063324_54188254 | FAM120C | chrX | 54063324 | 54188254 |
a0001c0001t0031g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM120C_chrX_54063324_54188254 | FAM120C | chrX | 54063324 | 54188254 |
a0001c0001t0031g0145 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM120C_chrX_54063324_54188254 | FAM120C | chrX | 54063324 | 54188254 |
a0001c0001t0032g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM120C_chrX_54063324_54188254 | FAM120C | chrX | 54063324 | 54188254 |
a0001c0001t0032g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM120C_chrX_54063324_54188254 | FAM120C | chrX | 54063324 | 54188254 |
a0001c0001t0033g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM120C_chrX_54063324_54188254 | FAM120C | chrX | 54063324 | 54188254 |
a0001c0001t0033g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM120C_chrX_54063324_54188254 | FAM120C | chrX | 54063324 | 54188254 |
a0001c0001t0035g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM120C_chrX_54063324_54188254 | FAM120C | chrX | 54063324 | 54188254 |
a0001c0001t0036g0078 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM120C_chrX_54063324_54188254 | FAM120C | chrX | 54063324 | 54188254 |
a0001c0001t0037g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM120C_chrX_54063324_54188254 | FAM120C | chrX | 54063324 | 54188254 |
a0001c0001t0038g0090 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM120C_chrX_54063324_54188254 | FAM120C | chrX | 54063324 | 54188254 |
a0001c0001t0039g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM120C_chrX_54063324_54188254 | FAM120C | chrX | 54063324 | 54188254 |
a0001c0001t0040g0039 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | FAM120C_chrX_54063324_54188254 | FAM120C | chrX | 54063324 | 54188254 |
a0001c0001t0041g0098 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM120C_chrX_54063324_54188254 | FAM120C | chrX | 54063324 | 54188254 |
a0001c0001t0042g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM120C_chrX_54063324_54188254 | FAM120C | chrX | 54063324 | 54188254 |
a0001c0001t0043g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM120C_chrX_54063324_54188254 | FAM120C | chrX | 54063324 | 54188254 |
a0001c0001t0044g0156 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM120C_chrX_54063324_54188254 | FAM120C | chrX | 54063324 | 54188254 |
a0001c0001t0045g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM120C_chrX_54063324_54188254 | FAM120C | chrX | 54063324 | 54188254 |
a0001c0001t0046g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM120C_chrX_54063324_54188254 | FAM120C | chrX | 54063324 | 54188254 |
a0001c0001t0048g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM120C_chrX_54063324_54188254 | FAM120C | chrX | 54063324 | 54188254 |
a0001c0001t0049g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM120C_chrX_54063324_54188254 | FAM120C | chrX | 54063324 | 54188254 |
a0001c0001t0050g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM120C_chrX_54063324_54188254 | FAM120C | chrX | 54063324 | 54188254 |
a0001c0001t0052g0100 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM120C_chrX_54063324_54188254 | FAM120C | chrX | 54063324 | 54188254 |
a0001c0001t0053g0099 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM120C_chrX_54063324_54188254 | FAM120C | chrX | 54063324 | 54188254 |
a0001c0001t0054g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM120C_chrX_54063324_54188254 | FAM120C | chrX | 54063324 | 54188254 |
a0001c0001t0055g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM120C_chrX_54063324_54188254 | FAM120C | chrX | 54063324 | 54188254 |
a0001c0001t0056g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM120C_chrX_54063324_54188254 | FAM120C | chrX | 54063324 | 54188254 |
a0001c0001t0057g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM120C_chrX_54063324_54188254 | FAM120C | chrX | 54063324 | 54188254 |
a0001c0001t0058g0020 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM120C_chrX_54063324_54188254 | FAM120C | chrX | 54063324 | 54188254 |
a0001c0001t0059g0024 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM120C_chrX_54063324_54188254 | FAM120C | chrX | 54063324 | 54188254 |
a0001c0001t0060g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM120C_chrX_54063324_54188254 | FAM120C | chrX | 54063324 | 54188254 |
a0001c0001t0061g0019 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM120C_chrX_54063324_54188254 | FAM120C | chrX | 54063324 | 54188254 |
a0001c0001t0062g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM120C_chrX_54063324_54188254 | FAM120C | chrX | 54063324 | 54188254 |
a0001c0001t0063g0009 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM120C_chrX_54063324_54188254 | FAM120C | chrX | 54063324 | 54188254 |
a0001c0001t0064g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM120C_chrX_54063324_54188254 | FAM120C | chrX | 54063324 | 54188254 |
a0001c0001t0065g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM120C_chrX_54063324_54188254 | FAM120C | chrX | 54063324 | 54188254 |
a0001c0001t0066g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM120C_chrX_54063324_54188254 | FAM120C | chrX | 54063324 | 54188254 |
a0001c0001t0067g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM120C_chrX_54063324_54188254 | FAM120C | chrX | 54063324 | 54188254 |
a0001c0001t0068g0096 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM120C_chrX_54063324_54188254 | FAM120C | chrX | 54063324 | 54188254 |
a0001c0001t0069g0074 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM120C_chrX_54063324_54188254 | FAM120C | chrX | 54063324 | 54188254 |
a0001c0001t0070g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM120C_chrX_54063324_54188254 | FAM120C | chrX | 54063324 | 54188254 |
a0001c0001t0072g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM120C_chrX_54063324_54188254 | FAM120C | chrX | 54063324 | 54188254 |
a0001c0001t0073g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM120C_chrX_54063324_54188254 | FAM120C | chrX | 54063324 | 54188254 |
a0001c0001t0074g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM120C_chrX_54063324_54188254 | FAM120C | chrX | 54063324 | 54188254 |
a0001c0005t0006g0004 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM120C_chrX_54063324_54188254 | FAM120C | chrX | 54063324 | 54188254 |
a0001c0009t0071g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM120C_chrX_54063324_54188254 | FAM120C | chrX | 54063324 | 54188254 |
a0002c0002t0001g0187 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM120C_chrX_54063324_54188254 | FAM120C | chrX | 54063324 | 54188254 |
a0002c0002t0007g0184 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM120C_chrX_54063324_54188254 | FAM120C | chrX | 54063324 | 54188254 |
a0002c0002t0019g0186 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM120C_chrX_54063324_54188254 | FAM120C | chrX | 54063324 | 54188254 |
a0002c0002t0047g0185 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM120C_chrX_54063324_54188254 | FAM120C | chrX | 54063324 | 54188254 |
a0003c0003t0013g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM120C_chrX_54063324_54188254 | FAM120C | chrX | 54063324 | 54188254 |
a0003c0003t0013g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM120C_chrX_54063324_54188254 | FAM120C | chrX | 54063324 | 54188254 |
a0004c0008t0009g0105 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM120C_chrX_54063324_54188254 | FAM120C | chrX | 54063324 | 54188254 |
a0005c0007t0034g0007 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM120C_chrX_54063324_54188254 | FAM120C | chrX | 54063324 | 54188254 |
a0006c0006t0001g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM120C_chrX_54063324_54188254 | FAM120C | chrX | 54063324 | 54188254 |
a0007c0004t0051g0003 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM120C_chrX_54063324_54188254 | FAM120C | chrX | 54063324 | 54188254 |
a0008c0010t0075g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM120C_chrX_54063324_54188254 | FAM120C | chrX | 54063324 | 54188254 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00140 | hp1 | a0001 | c0001 | t0023 | g0050 | EUR | GBR | FAM120C_chrX_54063324_54188254 | FAM120C | chrX | 54063324 | 54188254 |
HG00280 | hp1 | a0002 | c0002 | t0001 | g0187 | EUR | FIN | FAM120C_chrX_54063324_54188254 | FAM120C | chrX | 54063324 | 54188254 |
HG00558 | hp1 | a0001 | c0001 | t0005 | g0059 | EAS | CHS | FAM120C_chrX_54063324_54188254 | FAM120C | chrX | 54063324 | 54188254 |
HG00558 | hp2 | a0001 | c0001 | t0002 | g0174 | EAS | CHS | FAM120C_chrX_54063324_54188254 | FAM120C | chrX | 54063324 | 54188254 |
HG00609 | hp1 | a0001 | c0001 | t0074 | g0157 | EAS | CHS | FAM120C_chrX_54063324_54188254 | FAM120C | chrX | 54063324 | 54188254 |
HG00621 | hp1 | a0001 | c0001 | t0008 | g0158 | EAS | CHS | FAM120C_chrX_54063324_54188254 | FAM120C | chrX | 54063324 | 54188254 |
HG00642 | hp1 | a0002 | c0002 | t0047 | g0185 | AMR | PUR | FAM120C_chrX_54063324_54188254 | FAM120C | chrX | 54063324 | 54188254 |
HG00673 | hp1 | a0001 | c0001 | t0001 | g0022 | EAS | CHS | FAM120C_chrX_54063324_54188254 | FAM120C | chrX | 54063324 | 54188254 |
HG00735 | hp1 | a0001 | c0001 | t0053 | g0099 | AMR | PUR | FAM120C_chrX_54063324_54188254 | FAM120C | chrX | 54063324 | 54188254 |
HG00735 | hp2 | a0002 | c0002 | t0019 | g0186 | AMR | PUR | FAM120C_chrX_54063324_54188254 | FAM120C | chrX | 54063324 | 54188254 |
HG00738 | hp1 | a0001 | c0001 | t0052 | g0100 | AMR | PUR | FAM120C_chrX_54063324_54188254 | FAM120C | chrX | 54063324 | 54188254 |
HG01069 | hp1 | a0001 | c0001 | t0058 | g0020 | AMR | PUR | FAM120C_chrX_54063324_54188254 | FAM120C | chrX | 54063324 | 54188254 |
HG01070 | hp1 | a0001 | c0001 | t0004 | g0045 | AMR | PUR | FAM120C_chrX_54063324_54188254 | FAM120C | chrX | 54063324 | 54188254 |
HG01070 | hp2 | a0001 | c0001 | t0011 | g0164 | AMR | PUR | FAM120C_chrX_54063324_54188254 | FAM120C | chrX | 54063324 | 54188254 |
HG01074 | hp1 | a0001 | c0001 | t0011 | g0163 | AMR | PUR | FAM120C_chrX_54063324_54188254 | FAM120C | chrX | 54063324 | 54188254 |
HG01081 | hp1 | a0001 | c0001 | t0002 | g0132 | AMR | PUR | FAM120C_chrX_54063324_54188254 | FAM120C | chrX | 54063324 | 54188254 |
HG01081 | hp2 | a0001 | c0001 | t0004 | g0180 | AMR | PUR | FAM120C_chrX_54063324_54188254 | FAM120C | chrX | 54063324 | 54188254 |
HG01099 | hp1 | a0001 | c0001 | t0004 | g0069 | AMR | PUR | FAM120C_chrX_54063324_54188254 | FAM120C | chrX | 54063324 | 54188254 |
HG01106 | hp1 | a0001 | c0001 | t0003 | g0181 | AMR | PUR | FAM120C_chrX_54063324_54188254 | FAM120C | chrX | 54063324 | 54188254 |
HG01109 | hp1 | a0001 | c0001 | t0009 | g0070 | AMR | PUR | FAM120C_chrX_54063324_54188254 | FAM120C | chrX | 54063324 | 54188254 |
HG01167 | hp1 | a0001 | c0001 | t0017 | g0171 | AMR | PUR | FAM120C_chrX_54063324_54188254 | FAM120C | chrX | 54063324 | 54188254 |
HG01169 | hp1 | a0001 | c0001 | t0017 | g0005 | AMR | PUR | FAM120C_chrX_54063324_54188254 | FAM120C | chrX | 54063324 | 54188254 |
HG01169 | hp2 | a0001 | c0001 | t0036 | g0078 | AMR | PUR | FAM120C_chrX_54063324_54188254 | FAM120C | chrX | 54063324 | 54188254 |
HG01192 | hp1 | a0002 | c0002 | t0007 | g0184 | AMR | PUR | FAM120C_chrX_54063324_54188254 | FAM120C | chrX | 54063324 | 54188254 |
HG01243 | hp1 | a0001 | c0001 | t0041 | g0098 | AMR | PUR | FAM120C_chrX_54063324_54188254 | FAM120C | chrX | 54063324 | 54188254 |
HG01255 | hp1 | a0001 | c0001 | t0031 | g0145 | AMR | CLM | FAM120C_chrX_54063324_54188254 | FAM120C | chrX | 54063324 | 54188254 |
HG01256 | hp1 | a0001 | c0001 | t0014 | g0075 | AMR | CLM | FAM120C_chrX_54063324_54188254 | FAM120C | chrX | 54063324 | 54188254 |
HG01257 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | FAM120C_chrX_54063324_54188254 | FAM120C | chrX | 54063324 | 54188254 |
HG01257 | hp2 | a0001 | c0001 | t0017 | g0154 | AMR | CLM | FAM120C_chrX_54063324_54188254 | FAM120C | chrX | 54063324 | 54188254 |
HG01258 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | FAM120C_chrX_54063324_54188254 | FAM120C | chrX | 54063324 | 54188254 |
HG01261 | hp1 | a0001 | c0001 | t0004 | g0071 | AMR | CLM | FAM120C_chrX_54063324_54188254 | FAM120C | chrX | 54063324 | 54188254 |
HG01358 | hp1 | a0001 | c0001 | t0023 | g0089 | AMR | CLM | FAM120C_chrX_54063324_54188254 | FAM120C | chrX | 54063324 | 54188254 |
HG01433 | hp1 | a0001 | c0001 | t0003 | g0110 | AMR | CLM | FAM120C_chrX_54063324_54188254 | FAM120C | chrX | 54063324 | 54188254 |
HG01515 | hp1 | a0004 | c0008 | t0009 | g0105 | EUR | IBS | FAM120C_chrX_54063324_54188254 | FAM120C | chrX | 54063324 | 54188254 |
HG01884 | hp1 | a0001 | c0001 | t0015 | g0015 | AFR | ACB | FAM120C_chrX_54063324_54188254 | FAM120C | chrX | 54063324 | 54188254 |
HG01884 | hp2 | a0001 | c0001 | t0030 | g0140 | AFR | ACB | FAM120C_chrX_54063324_54188254 | FAM120C | chrX | 54063324 | 54188254 |
HG01928 | hp1 | a0001 | c0001 | t0004 | g0086 | AMR | PEL | FAM120C_chrX_54063324_54188254 | FAM120C | chrX | 54063324 | 54188254 |
HG01934 | hp1 | a0001 | c0001 | t0020 | g0002 | AMR | PEL | FAM120C_chrX_54063324_54188254 | FAM120C | chrX | 54063324 | 54188254 |
HG01943 | hp1 | a0001 | c0001 | t0028 | g0063 | AMR | PEL | FAM120C_chrX_54063324_54188254 | FAM120C | chrX | 54063324 | 54188254 |
HG01952 | hp1 | a0001 | c0001 | t0061 | g0019 | AMR | PEL | FAM120C_chrX_54063324_54188254 | FAM120C | chrX | 54063324 | 54188254 |
HG02015 | hp1 | a0001 | c0001 | t0002 | g0161 | EAS | KHV | FAM120C_chrX_54063324_54188254 | FAM120C | chrX | 54063324 | 54188254 |
HG02027 | hp1 | a0001 | c0001 | t0023 | g0109 | EAS | KHV | FAM120C_chrX_54063324_54188254 | FAM120C | chrX | 54063324 | 54188254 |
HG02040 | hp1 | a0001 | c0001 | t0002 | g0159 | EAS | KHV | FAM120C_chrX_54063324_54188254 | FAM120C | chrX | 54063324 | 54188254 |
HG02055 | hp1 | a0001 | c0001 | t0016 | g0141 | AFR | ACB | FAM120C_chrX_54063324_54188254 | FAM120C | chrX | 54063324 | 54188254 |
HG02056 | hp1 | a0001 | c0001 | t0009 | g0034 | EAS | KHV | FAM120C_chrX_54063324_54188254 | FAM120C | chrX | 54063324 | 54188254 |
HG02071 | hp1 | a0001 | c0001 | t0055 | g0048 | EAS | KHV | FAM120C_chrX_54063324_54188254 | FAM120C | chrX | 54063324 | 54188254 |
HG02074 | hp1 | a0001 | c0001 | t0064 | g0082 | EAS | KHV | FAM120C_chrX_54063324_54188254 | FAM120C | chrX | 54063324 | 54188254 |
HG02083 | hp1 | a0001 | c0001 | t0012 | g0104 | EAS | KHV | FAM120C_chrX_54063324_54188254 | FAM120C | chrX | 54063324 | 54188254 |
HG02129 | hp1 | a0001 | c0001 | t0046 | g0085 | EAS | KHV | FAM120C_chrX_54063324_54188254 | FAM120C | chrX | 54063324 | 54188254 |
HG02132 | hp1 | a0001 | c0001 | t0011 | g0155 | EAS | KHV | FAM120C_chrX_54063324_54188254 | FAM120C | chrX | 54063324 | 54188254 |
HG02135 | hp1 | a0001 | c0001 | t0065 | g0083 | EAS | KHV | FAM120C_chrX_54063324_54188254 | FAM120C | chrX | 54063324 | 54188254 |
HG02145 | hp1 | a0001 | c0001 | t0026 | g0102 | AFR | ACB | FAM120C_chrX_54063324_54188254 | FAM120C | chrX | 54063324 | 54188254 |
HG02257 | hp1 | a0001 | c0001 | t0067 | g0018 | AFR | ACB | FAM120C_chrX_54063324_54188254 | FAM120C | chrX | 54063324 | 54188254 |
HG02257 | hp2 | a0001 | c0001 | t0017 | g0176 | AFR | ACB | FAM120C_chrX_54063324_54188254 | FAM120C | chrX | 54063324 | 54188254 |
HG02258 | hp1 | a0001 | c0001 | t0011 | g0123 | AFR | ACB | FAM120C_chrX_54063324_54188254 | FAM120C | chrX | 54063324 | 54188254 |
HG02300 | hp1 | a0001 | c0001 | t0003 | g0087 | AMR | PEL | FAM120C_chrX_54063324_54188254 | FAM120C | chrX | 54063324 | 54188254 |
HG02451 | hp1 | a0001 | c0001 | t0008 | g0125 | AFR | ACB | FAM120C_chrX_54063324_54188254 | FAM120C | chrX | 54063324 | 54188254 |
HG02451 | hp2 | a0001 | c0001 | t0016 | g0137 | AFR | ACB | FAM120C_chrX_54063324_54188254 | FAM120C | chrX | 54063324 | 54188254 |
HG02572 | hp1 | a0001 | c0001 | t0049 | g0152 | AFR | GWD | FAM120C_chrX_54063324_54188254 | FAM120C | chrX | 54063324 | 54188254 |
HG02602 | hp1 | a0001 | c0001 | t0014 | g0094 | SAS | PJL | FAM120C_chrX_54063324_54188254 | FAM120C | chrX | 54063324 | 54188254 |
HG02615 | hp1 | a0001 | c0001 | t0003 | g0084 | AFR | GWD | FAM120C_chrX_54063324_54188254 | FAM120C | chrX | 54063324 | 54188254 |
HG02615 | hp2 | a0001 | c0001 | t0042 | g0183 | AFR | GWD | FAM120C_chrX_54063324_54188254 | FAM120C | chrX | 54063324 | 54188254 |
HG02630 | hp1 | a0001 | c0001 | t0013 | g0112 | AFR | GWD | FAM120C_chrX_54063324_54188254 | FAM120C | chrX | 54063324 | 54188254 |
HG02630 | hp2 | a0001 | c0001 | t0025 | g0146 | AFR | GWD | FAM120C_chrX_54063324_54188254 | FAM120C | chrX | 54063324 | 54188254 |
HG02647 | hp1 | a0001 | c0001 | t0033 | g0013 | AFR | GWD | FAM120C_chrX_54063324_54188254 | FAM120C | chrX | 54063324 | 54188254 |
HG02698 | hp1 | a0001 | c0001 | t0044 | g0156 | SAS | PJL | FAM120C_chrX_54063324_54188254 | FAM120C | chrX | 54063324 | 54188254 |
HG02717 | hp1 | a0001 | c0001 | t0022 | g0016 | AFR | GWD | FAM120C_chrX_54063324_54188254 | FAM120C | chrX | 54063324 | 54188254 |
HG02735 | hp1 | a0001 | c0001 | t0014 | g0093 | SAS | PJL | FAM120C_chrX_54063324_54188254 | FAM120C | chrX | 54063324 | 54188254 |
HG02738 | hp1 | a0001 | c0001 | t0009 | g0033 | SAS | PJL | FAM120C_chrX_54063324_54188254 | FAM120C | chrX | 54063324 | 54188254 |
HG02809 | hp1 | a0001 | c0001 | t0072 | g0106 | AFR | GWD | FAM120C_chrX_54063324_54188254 | FAM120C | chrX | 54063324 | 54188254 |
HG02809 | hp2 | a0001 | c0001 | t0018 | g0115 | AFR | GWD | FAM120C_chrX_54063324_54188254 | FAM120C | chrX | 54063324 | 54188254 |
HG02895 | hp1 | a0001 | c0001 | t0025 | g0135 | AFR | GWD | FAM120C_chrX_54063324_54188254 | FAM120C | chrX | 54063324 | 54188254 |
HG02896 | hp1 | a0001 | c0001 | t0015 | g0136 | AFR | GWD | FAM120C_chrX_54063324_54188254 | FAM120C | chrX | 54063324 | 54188254 |
HG02896 | hp2 | a0001 | c0001 | t0013 | g0130 | AFR | GWD | FAM120C_chrX_54063324_54188254 | FAM120C | chrX | 54063324 | 54188254 |
HG02922 | hp1 | a0001 | c0001 | t0016 | g0139 | AFR | ESN | FAM120C_chrX_54063324_54188254 | FAM120C | chrX | 54063324 | 54188254 |
HG02922 | hp2 | a0001 | c0001 | t0043 | g0147 | AFR | ESN | FAM120C_chrX_54063324_54188254 | FAM120C | chrX | 54063324 | 54188254 |
HG02965 | hp1 | a0001 | c0001 | t0048 | g0126 | AFR | ESN | FAM120C_chrX_54063324_54188254 | FAM120C | chrX | 54063324 | 54188254 |
HG03017 | hp1 | a0001 | c0001 | t0059 | g0024 | SAS | PJL | FAM120C_chrX_54063324_54188254 | FAM120C | chrX | 54063324 | 54188254 |
HG03098 | hp1 | a0003 | c0003 | t0013 | g0121 | AFR | MSL | FAM120C_chrX_54063324_54188254 | FAM120C | chrX | 54063324 | 54188254 |
HG03130 | hp1 | a0001 | c0001 | t0054 | g0144 | AFR | ESN | FAM120C_chrX_54063324_54188254 | FAM120C | chrX | 54063324 | 54188254 |
HG03139 | hp1 | a0001 | c0001 | t0020 | g0002 | AFR | ESN | FAM120C_chrX_54063324_54188254 | FAM120C | chrX | 54063324 | 54188254 |
HG03209 | hp1 | a0001 | c0001 | t0056 | g0103 | AFR | MSL | FAM120C_chrX_54063324_54188254 | FAM120C | chrX | 54063324 | 54188254 |
HG03225 | hp1 | a0001 | c0001 | t0060 | g0134 | AFR | MSL | FAM120C_chrX_54063324_54188254 | FAM120C | chrX | 54063324 | 54188254 |
HG03453 | hp1 | a0007 | c0004 | t0051 | g0003 | AFR | MSL | FAM120C_chrX_54063324_54188254 | FAM120C | chrX | 54063324 | 54188254 |
HG03453 | hp2 | a0001 | c0001 | t0015 | g0133 | AFR | MSL | FAM120C_chrX_54063324_54188254 | FAM120C | chrX | 54063324 | 54188254 |
HG03486 | hp1 | a0001 | c0001 | t0016 | g0142 | AFR | MSL | FAM120C_chrX_54063324_54188254 | FAM120C | chrX | 54063324 | 54188254 |
HG03486 | hp2 | a0001 | c0001 | t0019 | g0120 | AFR | MSL | FAM120C_chrX_54063324_54188254 | FAM120C | chrX | 54063324 | 54188254 |
HG03490 | hp1 | a0001 | c0001 | t0012 | g0043 | SAS | PJL | FAM120C_chrX_54063324_54188254 | FAM120C | chrX | 54063324 | 54188254 |
HG03492 | hp1 | a0001 | c0001 | t0029 | g0088 | SAS | PJL | FAM120C_chrX_54063324_54188254 | FAM120C | chrX | 54063324 | 54188254 |
HG03516 | hp1 | a0001 | c0001 | t0022 | g0149 | AFR | ESN | FAM120C_chrX_54063324_54188254 | FAM120C | chrX | 54063324 | 54188254 |
HG03516 | hp2 | a0001 | c0001 | t0019 | g0111 | AFR | ESN | FAM120C_chrX_54063324_54188254 | FAM120C | chrX | 54063324 | 54188254 |
HG03579 | hp1 | a0003 | c0003 | t0013 | g0122 | AFR | MSL | FAM120C_chrX_54063324_54188254 | FAM120C | chrX | 54063324 | 54188254 |
HG03654 | hp1 | a0001 | c0001 | t0038 | g0090 | SAS | PJL | FAM120C_chrX_54063324_54188254 | FAM120C | chrX | 54063324 | 54188254 |
HG03688 | hp1 | a0001 | c0001 | t0024 | g0080 | SAS | STU | FAM120C_chrX_54063324_54188254 | FAM120C | chrX | 54063324 | 54188254 |
HG03710 | hp1 | a0001 | c0001 | t0003 | g0107 | SAS | PJL | FAM120C_chrX_54063324_54188254 | FAM120C | chrX | 54063324 | 54188254 |
HG03942 | hp1 | a0001 | c0001 | t0012 | g0035 | SAS | BEB | FAM120C_chrX_54063324_54188254 | FAM120C | chrX | 54063324 | 54188254 |
HG04115 | hp1 | a0001 | c0001 | t0014 | g0046 | SAS | STU | FAM120C_chrX_54063324_54188254 | FAM120C | chrX | 54063324 | 54188254 |
HG04199 | hp1 | a0001 | c0001 | t0003 | g0038 | SAS | STU | FAM120C_chrX_54063324_54188254 | FAM120C | chrX | 54063324 | 54188254 |
HG04204 | hp1 | a0001 | c0001 | t0068 | g0096 | SAS | STU | FAM120C_chrX_54063324_54188254 | FAM120C | chrX | 54063324 | 54188254 |
HG04228 | hp1 | a0001 | c0001 | t0012 | g0047 | SAS | STU | FAM120C_chrX_54063324_54188254 | FAM120C | chrX | 54063324 | 54188254 |
NA18522 | hp1 | a0001 | c0001 | t0027 | g0117 | AFR | YRI | FAM120C_chrX_54063324_54188254 | FAM120C | chrX | 54063324 | 54188254 |
NA18612 | hp1 | a0001 | c0001 | t0010 | g0091 | EAS | CHB | FAM120C_chrX_54063324_54188254 | FAM120C | chrX | 54063324 | 54188254 |
NA18747 | hp1 | a0001 | c0001 | t0007 | g0054 | EAS | CHB | FAM120C_chrX_54063324_54188254 | FAM120C | chrX | 54063324 | 54188254 |
NA18906 | hp1 | a0001 | c0001 | t0030 | g0143 | AFR | YRI | FAM120C_chrX_54063324_54188254 | FAM120C | chrX | 54063324 | 54188254 |
NA18906 | hp2 | a0001 | c0001 | t0039 | g0150 | AFR | YRI | FAM120C_chrX_54063324_54188254 | FAM120C | chrX | 54063324 | 54188254 |
NA18940 | hp1 | a0001 | c0001 | t0001 | g0036 | EAS | JPT | FAM120C_chrX_54063324_54188254 | FAM120C | chrX | 54063324 | 54188254 |
NA18943 | hp1 | a0001 | c0001 | t0007 | g0057 | EAS | JPT | FAM120C_chrX_54063324_54188254 | FAM120C | chrX | 54063324 | 54188254 |
NA18944 | hp1 | a0001 | c0001 | t0001 | g0052 | EAS | JPT | FAM120C_chrX_54063324_54188254 | FAM120C | chrX | 54063324 | 54188254 |
NA18945 | hp1 | a0001 | c0001 | t0001 | g0044 | EAS | JPT | FAM120C_chrX_54063324_54188254 | FAM120C | chrX | 54063324 | 54188254 |
NA18948 | hp1 | a0001 | c0001 | t0024 | g0067 | EAS | JPT | FAM120C_chrX_54063324_54188254 | FAM120C | chrX | 54063324 | 54188254 |
NA18950 | hp1 | a0001 | c0001 | t0002 | g0168 | EAS | JPT | FAM120C_chrX_54063324_54188254 | FAM120C | chrX | 54063324 | 54188254 |
NA18950 | hp2 | a0006 | c0006 | t0001 | g0128 | EAS | JPT | FAM120C_chrX_54063324_54188254 | FAM120C | chrX | 54063324 | 54188254 |
NA18952 | hp1 | a0001 | c0001 | t0050 | g0051 | EAS | JPT | FAM120C_chrX_54063324_54188254 | FAM120C | chrX | 54063324 | 54188254 |
NA18953 | hp1 | a0001 | c0001 | t0021 | g0014 | EAS | JPT | FAM120C_chrX_54063324_54188254 | FAM120C | chrX | 54063324 | 54188254 |
NA18957 | hp1 | a0001 | c0001 | t0002 | g0160 | EAS | JPT | FAM120C_chrX_54063324_54188254 | FAM120C | chrX | 54063324 | 54188254 |
NA18957 | hp2 | a0001 | c0001 | t0021 | g0056 | EAS | JPT | FAM120C_chrX_54063324_54188254 | FAM120C | chrX | 54063324 | 54188254 |
NA18959 | hp1 | a0001 | c0005 | t0006 | g0004 | EAS | JPT | FAM120C_chrX_54063324_54188254 | FAM120C | chrX | 54063324 | 54188254 |
NA18960 | hp1 | a0001 | c0001 | t0002 | g0166 | EAS | JPT | FAM120C_chrX_54063324_54188254 | FAM120C | chrX | 54063324 | 54188254 |
NA18962 | hp1 | a0001 | c0001 | t0063 | g0009 | EAS | JPT | FAM120C_chrX_54063324_54188254 | FAM120C | chrX | 54063324 | 54188254 |
NA18965 | hp1 | a0001 | c0001 | t0037 | g0129 | EAS | JPT | FAM120C_chrX_54063324_54188254 | FAM120C | chrX | 54063324 | 54188254 |
NA18966 | hp1 | a0001 | c0001 | t0057 | g0173 | EAS | JPT | FAM120C_chrX_54063324_54188254 | FAM120C | chrX | 54063324 | 54188254 |
NA18967 | hp1 | a0001 | c0001 | t0010 | g0092 | EAS | JPT | FAM120C_chrX_54063324_54188254 | FAM120C | chrX | 54063324 | 54188254 |
NA18969 | hp1 | a0001 | c0001 | t0010 | g0072 | EAS | JPT | FAM120C_chrX_54063324_54188254 | FAM120C | chrX | 54063324 | 54188254 |
NA18969 | hp2 | a0001 | c0001 | t0008 | g0162 | EAS | JPT | FAM120C_chrX_54063324_54188254 | FAM120C | chrX | 54063324 | 54188254 |
NA18970 | hp1 | a0001 | c0001 | t0001 | g0027 | EAS | JPT | FAM120C_chrX_54063324_54188254 | FAM120C | chrX | 54063324 | 54188254 |
NA18971 | hp1 | a0001 | c0001 | t0010 | g0065 | EAS | JPT | FAM120C_chrX_54063324_54188254 | FAM120C | chrX | 54063324 | 54188254 |
NA18972 | hp1 | a0001 | c0001 | t0032 | g0178 | EAS | JPT | FAM120C_chrX_54063324_54188254 | FAM120C | chrX | 54063324 | 54188254 |
NA18972 | hp2 | a0001 | c0001 | t0035 | g0114 | EAS | JPT | FAM120C_chrX_54063324_54188254 | FAM120C | chrX | 54063324 | 54188254 |
NA18973 | hp1 | a0001 | c0001 | t0032 | g0108 | EAS | JPT | FAM120C_chrX_54063324_54188254 | FAM120C | chrX | 54063324 | 54188254 |
NA18973 | hp2 | a0001 | c0001 | t0001 | g0177 | EAS | JPT | FAM120C_chrX_54063324_54188254 | FAM120C | chrX | 54063324 | 54188254 |
NA18977 | hp1 | a0001 | c0001 | t0005 | g0113 | EAS | JPT | FAM120C_chrX_54063324_54188254 | FAM120C | chrX | 54063324 | 54188254 |
NA18980 | hp1 | a0001 | c0001 | t0011 | g0010 | EAS | JPT | FAM120C_chrX_54063324_54188254 | FAM120C | chrX | 54063324 | 54188254 |
NA18980 | hp2 | a0001 | c0001 | t0010 | g0175 | EAS | JPT | FAM120C_chrX_54063324_54188254 | FAM120C | chrX | 54063324 | 54188254 |
NA18982 | hp1 | a0001 | c0001 | t0021 | g0077 | EAS | JPT | FAM120C_chrX_54063324_54188254 | FAM120C | chrX | 54063324 | 54188254 |
NA18983 | hp1 | a0001 | c0001 | t0005 | g0058 | EAS | JPT | FAM120C_chrX_54063324_54188254 | FAM120C | chrX | 54063324 | 54188254 |
NA18984 | hp1 | a0001 | c0001 | t0012 | g0127 | EAS | JPT | FAM120C_chrX_54063324_54188254 | FAM120C | chrX | 54063324 | 54188254 |
NA18985 | hp1 | a0001 | c0001 | t0005 | g0095 | EAS | JPT | FAM120C_chrX_54063324_54188254 | FAM120C | chrX | 54063324 | 54188254 |
NA18986 | hp1 | a0001 | c0001 | t0003 | g0032 | EAS | JPT | FAM120C_chrX_54063324_54188254 | FAM120C | chrX | 54063324 | 54188254 |
NA18988 | hp1 | a0001 | c0001 | t0006 | g0053 | EAS | JPT | FAM120C_chrX_54063324_54188254 | FAM120C | chrX | 54063324 | 54188254 |
NA18989 | hp1 | a0001 | c0009 | t0071 | g0031 | EAS | JPT | FAM120C_chrX_54063324_54188254 | FAM120C | chrX | 54063324 | 54188254 |
NA18990 | hp1 | a0001 | c0001 | t0006 | g0030 | EAS | JPT | FAM120C_chrX_54063324_54188254 | FAM120C | chrX | 54063324 | 54188254 |
NA18994 | hp1 | a0001 | c0001 | t0003 | g0041 | EAS | JPT | FAM120C_chrX_54063324_54188254 | FAM120C | chrX | 54063324 | 54188254 |
NA18995 | hp1 | a0001 | c0001 | t0007 | g0055 | EAS | JPT | FAM120C_chrX_54063324_54188254 | FAM120C | chrX | 54063324 | 54188254 |
NA18998 | hp1 | a0001 | c0001 | t0001 | g0025 | EAS | JPT | FAM120C_chrX_54063324_54188254 | FAM120C | chrX | 54063324 | 54188254 |
NA18998 | hp2 | a0001 | c0001 | t0002 | g0169 | EAS | JPT | FAM120C_chrX_54063324_54188254 | FAM120C | chrX | 54063324 | 54188254 |
NA19000 | hp1 | a0001 | c0001 | t0005 | g0037 | EAS | JPT | FAM120C_chrX_54063324_54188254 | FAM120C | chrX | 54063324 | 54188254 |
NA19004 | hp1 | a0001 | c0001 | t0007 | g0081 | EAS | JPT | FAM120C_chrX_54063324_54188254 | FAM120C | chrX | 54063324 | 54188254 |
NA19005 | hp1 | a0001 | c0001 | t0001 | g0079 | EAS | JPT | FAM120C_chrX_54063324_54188254 | FAM120C | chrX | 54063324 | 54188254 |
NA19007 | hp1 | a0001 | c0001 | t0002 | g0167 | EAS | JPT | FAM120C_chrX_54063324_54188254 | FAM120C | chrX | 54063324 | 54188254 |
NA19009 | hp1 | a0001 | c0001 | t0001 | g0061 | EAS | JPT | FAM120C_chrX_54063324_54188254 | FAM120C | chrX | 54063324 | 54188254 |
NA19012 | hp1 | a0001 | c0001 | t0003 | g0040 | EAS | JPT | FAM120C_chrX_54063324_54188254 | FAM120C | chrX | 54063324 | 54188254 |
NA19030 | hp1 | a0001 | c0001 | t0026 | g0101 | AFR | LWK | FAM120C_chrX_54063324_54188254 | FAM120C | chrX | 54063324 | 54188254 |
NA19030 | hp2 | a0001 | c0001 | t0020 | g0131 | AFR | LWK | FAM120C_chrX_54063324_54188254 | FAM120C | chrX | 54063324 | 54188254 |
NA19043 | hp1 | a0001 | c0001 | t0018 | g0151 | AFR | LWK | FAM120C_chrX_54063324_54188254 | FAM120C | chrX | 54063324 | 54188254 |
NA19055 | hp1 | a0008 | c0010 | t0075 | g0188 | EAS | JPT | FAM120C_chrX_54063324_54188254 | FAM120C | chrX | 54063324 | 54188254 |
NA19056 | hp1 | a0001 | c0001 | t0009 | g0073 | EAS | JPT | FAM120C_chrX_54063324_54188254 | FAM120C | chrX | 54063324 | 54188254 |
NA19058 | hp1 | a0001 | c0001 | t0005 | g0062 | EAS | JPT | FAM120C_chrX_54063324_54188254 | FAM120C | chrX | 54063324 | 54188254 |
NA19060 | hp1 | a0001 | c0001 | t0004 | g0021 | EAS | JPT | FAM120C_chrX_54063324_54188254 | FAM120C | chrX | 54063324 | 54188254 |
NA19062 | hp1 | a0001 | c0001 | t0010 | g0023 | EAS | JPT | FAM120C_chrX_54063324_54188254 | FAM120C | chrX | 54063324 | 54188254 |
NA19066 | hp1 | a0001 | c0001 | t0001 | g0060 | EAS | JPT | FAM120C_chrX_54063324_54188254 | FAM120C | chrX | 54063324 | 54188254 |
NA19067 | hp1 | a0001 | c0001 | t0062 | g0182 | EAS | JPT | FAM120C_chrX_54063324_54188254 | FAM120C | chrX | 54063324 | 54188254 |
NA19068 | hp1 | a0001 | c0001 | t0001 | g0042 | EAS | JPT | FAM120C_chrX_54063324_54188254 | FAM120C | chrX | 54063324 | 54188254 |
NA19070 | hp1 | a0001 | c0001 | t0007 | g0017 | EAS | JPT | FAM120C_chrX_54063324_54188254 | FAM120C | chrX | 54063324 | 54188254 |
NA19075 | hp1 | a0005 | c0007 | t0034 | g0007 | EAS | JPT | FAM120C_chrX_54063324_54188254 | FAM120C | chrX | 54063324 | 54188254 |
NA19077 | hp1 | a0001 | c0001 | t0008 | g0165 | EAS | JPT | FAM120C_chrX_54063324_54188254 | FAM120C | chrX | 54063324 | 54188254 |
NA19077 | hp2 | a0001 | c0001 | t0005 | g0011 | EAS | JPT | FAM120C_chrX_54063324_54188254 | FAM120C | chrX | 54063324 | 54188254 |
NA19078 | hp1 | a0001 | c0001 | t0073 | g0179 | EAS | JPT | FAM120C_chrX_54063324_54188254 | FAM120C | chrX | 54063324 | 54188254 |
NA19078 | hp2 | a0001 | c0001 | t0002 | g0153 | EAS | JPT | FAM120C_chrX_54063324_54188254 | FAM120C | chrX | 54063324 | 54188254 |
NA19079 | hp1 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | FAM120C_chrX_54063324_54188254 | FAM120C | chrX | 54063324 | 54188254 |
NA19082 | hp1 | a0001 | c0001 | t0008 | g0170 | EAS | JPT | FAM120C_chrX_54063324_54188254 | FAM120C | chrX | 54063324 | 54188254 |
NA19083 | hp1 | a0001 | c0001 | t0009 | g0049 | EAS | JPT | FAM120C_chrX_54063324_54188254 | FAM120C | chrX | 54063324 | 54188254 |
NA19085 | hp1 | a0001 | c0001 | t0006 | g0028 | EAS | JPT | FAM120C_chrX_54063324_54188254 | FAM120C | chrX | 54063324 | 54188254 |
NA19086 | hp1 | a0001 | c0001 | t0004 | g0006 | EAS | JPT | FAM120C_chrX_54063324_54188254 | FAM120C | chrX | 54063324 | 54188254 |
NA19088 | hp1 | a0001 | c0001 | t0006 | g0029 | EAS | JPT | FAM120C_chrX_54063324_54188254 | FAM120C | chrX | 54063324 | 54188254 |
NA19089 | hp1 | a0001 | c0001 | t0066 | g0076 | EAS | JPT | FAM120C_chrX_54063324_54188254 | FAM120C | chrX | 54063324 | 54188254 |
NA19091 | hp1 | a0001 | c0001 | t0070 | g0064 | EAS | JPT | FAM120C_chrX_54063324_54188254 | FAM120C | chrX | 54063324 | 54188254 |
NA20129 | hp1 | a0001 | c0001 | t0015 | g0097 | AFR | ASW | FAM120C_chrX_54063324_54188254 | FAM120C | chrX | 54063324 | 54188254 |
NA20129 | hp2 | a0001 | c0001 | t0022 | g0119 | AFR | ASW | FAM120C_chrX_54063324_54188254 | FAM120C | chrX | 54063324 | 54188254 |
NA20752 | hp1 | a0001 | c0001 | t0029 | g0068 | EUR | TSI | FAM120C_chrX_54063324_54188254 | FAM120C | chrX | 54063324 | 54188254 |
NA20805 | hp1 | a0001 | c0001 | t0028 | g0066 | EUR | TSI | FAM120C_chrX_54063324_54188254 | FAM120C | chrX | 54063324 | 54188254 |
NA20905 | hp1 | a0001 | c0001 | t0069 | g0074 | SAS | GIH | FAM120C_chrX_54063324_54188254 | FAM120C | chrX | 54063324 | 54188254 |
HG02486 | hp1 | a0001 | c0001 | t0031 | g0138 | AFR | ACB | FAM120C_chrX_54063324_54188254 | FAM120C | chrX | 54063324 | 54188254 |
HG02559 | hp1 | a0001 | c0001 | t0008 | g0124 | AFR | ACB | FAM120C_chrX_54063324_54188254 | FAM120C | chrX | 54063324 | 54188254 |
HG02559 | hp2 | a0001 | c0001 | t0033 | g0012 | AFR | ACB | FAM120C_chrX_54063324_54188254 | FAM120C | chrX | 54063324 | 54188254 |
HG03471 | hp1 | a0001 | c0001 | t0045 | g0148 | AFR | MSL | FAM120C_chrX_54063324_54188254 | FAM120C | chrX | 54063324 | 54188254 |
HG06807 | hp1 | a0001 | c0001 | t0018 | g0116 | AFR | USA | FAM120C_chrX_54063324_54188254 | FAM120C | chrX | 54063324 | 54188254 |
HG06807 | hp2 | a0001 | c0001 | t0027 | g0118 | AFR | USA | FAM120C_chrX_54063324_54188254 | FAM120C | chrX | 54063324 | 54188254 |
NA18955 | hp1 | a0001 | c0001 | t0006 | g0026 | EAS | JPT | FAM120C_chrX_54063324_54188254 | FAM120C | chrX | 54063324 | 54188254 |
homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0002 | g0172 | REF | REF | FAM120C_chrX_54063324_54188254 | FAM120C | chrX | 54063324 | 54188254 |
homoSapiens_grch38 | hp1 | a0001 | c0001 | t0040 | g0039 | REF | REF | FAM120C_chrX_54063324_54188254 | FAM120C | chrX | 54063324 | 54188254 |
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:54085752
|
C | T | 1 | a0004 | 1 | HG01515.hp1 | missense_variant | MODERATE | c.2802G>A | p.Met934Ile | FAM120C | ENSG00000184083.12 | transcript | ENST00000375180.7 | protein_coding | 13/16 | 2858/8056 | 2802/3291 | 934/1096 | chrX | 54085752 | ||
chrX:54085763
|
T | C | 1 | a0003 | 2 | HG03098.hp1 HG03579.hp1 |
missense_variant | MODERATE | c.2791A>G | p.Met931Val | FAM120C | ENSG00000184083.12 | transcript | ENST00000375180.7 | protein_coding | 13/16 | 2847/8056 | 2791/3291 | 931/1096 | chrX | 54085763 | ||
chrX:54132709
|
C | CA | 1 | a0005 | 1 | NA19075.hp1 | frameshift_variant | HIGH | c.2044_2045insT | p.Arg682fs | FAM120C | ENSG00000184083.12 | transcript | ENST00000375180.7 | protein_coding | 9/16 | 2100/8056 | 2044/3291 | 682/1096 | chrX | 54132709 | ||
chrX:54132790
|
CG | C | 1 | a0005 | 1 | NA19075.hp1 | frameshift_variant | HIGH | c.1963delC | p.Arg655fs | FAM120C | ENSG00000184083.12 | transcript | ENST00000375180.7 | protein_coding | 9/16 | 2019/8056 | 1963/3291 | 655/1096 | chrX | 54132790 | ||
chrX:54132795
|
TA | T | 1 | a0005 | 1 | NA19075.hp1 | frameshift_variant | HIGH | c.1958delT | p.Leu653fs | FAM120C | ENSG00000184083.12 | transcript | ENST00000375180.7 | protein_coding | 9/16 | 2014/8056 | 1958/3291 | 653/1096 | chrX | 54132795 | ||
chrX:54132832
|
T | TC | 1 | a0005 | 1 | NA19075.hp1 | frameshift_variant | HIGH | c.1921dupG | p.Asp641fs | FAM120C | ENSG00000184083.12 | transcript | ENST00000375180.7 | protein_coding | 9/16 | 1977/8056 | 1921/3291 | 641/1096 | chrX | 54132832 | ||
chrX:54132847
|
G | A | 1 | a0005 | 1 | NA19075.hp1 | missense_variant | MODERATE | c.1907C>T | p.Pro636Leu | FAM120C | ENSG00000184083.12 | transcript | ENST00000375180.7 | protein_coding | 9/16 | 1963/8056 | 1907/3291 | 636/1096 | chrX | 54132847 | ||
chrX:54133865
|
AG | A | 1 | a0005 | 1 | NA19075.hp1 | frameshift_variant | HIGH | c.1797delC | p.Leu600fs | FAM120C | ENSG00000184083.12 | transcript | ENST00000375180.7 | protein_coding | 8/16 | 1853/8056 | 1797/3291 | 599/1096 | chrX | 54133865 | ||
chrX:54133938
|
A | AC | 1 | a0005 | 1 | NA19075.hp1 | frameshift_variant | HIGH | c.1724dupG | p.Asp576fs | FAM120C | ENSG00000184083.12 | transcript | ENST00000375180.7 | protein_coding | 8/16 | 1780/8056 | 1724/3291 | 575/1096 | chrX | 54133938 | ||
chrX:54133978
|
GC | G | 1 | a0005 | 1 | NA19075.hp1 | frameshift_variant | HIGH | c.1684delG | p.Ala562fs | FAM120C | ENSG00000184083.12 | transcript | ENST00000375180.7 | protein_coding | 8/16 | 1740/8056 | 1684/3291 | 562/1096 | chrX | 54133978 | ||
chrX:54134003
|
G | A | 1 | a0005 | 1 | NA19075.hp1 | missense_variant | MODERATE | c.1660C>T | p.Pro554Ser | FAM120C | ENSG00000184083.12 | transcript | ENST00000375180.7 | protein_coding | 8/16 | 1716/8056 | 1660/3291 | 554/1096 | chrX | 54134003 | ||
chrX:54134004
|
A | T | 1 | a0005 | 1 | NA19075.hp1 | missense_variant | MODERATE | c.1659T>A | p.Asn553Lys | FAM120C | ENSG00000184083.12 | transcript | ENST00000375180.7 | protein_coding | 8/16 | 1715/8056 | 1659/3291 | 553/1096 | chrX | 54134004 | ||
chrX:54134933
|
TG | T | 1 | a0005 | 1 | NA19075.hp1 | frameshift_variant | HIGH | c.1513delC | p.Gln505fs | FAM120C | ENSG00000184083.12 | transcript | ENST00000375180.7 | protein_coding | 7/16 | 1569/8056 | 1513/3291 | 505/1096 | chrX | 54134933 | ||
chrX:54135011
|
TG | T | 1 | a0005 | 1 | NA19075.hp1 | frameshift_variant | HIGH | c.1435delC | p.His479fs | FAM120C | ENSG00000184083.12 | transcript | ENST00000375180.7 | protein_coding | 7/16 | 1491/8056 | 1435/3291 | 479/1096 | chrX | 54135011 | ||
chrX:54135017
|
TC | T | 1 | a0006 | 1 | NA18950.hp2 | frameshift_variant | HIGH | c.1429delG | p.Glu477fs | FAM120C | ENSG00000184083.12 | transcript | ENST00000375180.7 | protein_coding | 7/16 | 1485/8056 | 1429/3291 | 477/1096 | chrX | 54135017 | ||
chrX:54182716
|
GC | G | 1 | a0008 | 1 | NA19055.hp1 | frameshift_variant | HIGH | c.482delG | p.Gly161fs | FAM120C | ENSG00000184083.12 | transcript | ENST00000375180.7 | protein_coding | 1/16 | 538/8056 | 482/3291 | 161/1096 | chrX | 54182716 | ||
chrX:54182869
|
G | GGGCGGC | 1 | a0002 | 4 | HG00280.hp1 HG00642.hp1 HG00735.hp2 others(1): Show |
disruptive_inframe_insertion | MODERATE | c.324_329dupGCCGCC | p.Pro109_Pro110dup | FAM120C | ENSG00000184083.12 | transcript | ENST00000375180.7 | protein_coding | 1/16 | 385/8056 | 329/3291 | 110/1096 | chrX | 54182869 | ||
chrX:54183068
|
G | T | 1 | a0007 | 1 | HG03453.hp1 | missense_variant | MODERATE | c.131C>A | p.Pro44Gln | FAM120C | ENSG00000184083.12 | transcript | ENST00000375180.7 | protein_coding | 1/16 | 187/8056 | 131/3291 | 44/1096 | chrX | 54183068 | ||
chrX:54183088
|
C | CTG | 1 | a0008 | 1 | NA19055.hp1 | frameshift_variant | HIGH | c.109_110dupCA | p.Gln37fs | FAM120C | ENSG00000184083.12 | transcript | ENST00000375180.7 | protein_coding | 1/16 | 166/8056 | 110/3291 | 37/1096 | chrX | 54183088 | ||
chrX:54183149
|
G | GC | 1 | a0008 | 1 | NA19055.hp1 | frameshift_variant | HIGH | c.49dupG | p.Ala17fs | FAM120C | ENSG00000184083.12 | transcript | ENST00000375180.7 | protein_coding | 1/16 | 105/8056 | 49/3291 | 17/1096 | chrX | 54183149 |
chr:pos | ref | alt | # # of chapid |
chapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chrX:54073219
|
T | G | 3 | a0001c0005a0001c0009a0008c0010 | 3 | NA18959.hp1 NA18989.hp1 NA19055.hp1 |
synonymous_variant | LOW | c.3105A>C | p.Gly1035Gly | FAM120C | ENSG00000184083.12 | transcript | ENST00000375180.7 | protein_coding | 16/16 | 3161/8056 | 3105/3291 | 1035/1096 | chrX | 54073219 | ||
chrX:54091339
|
A | G | 1 | a0006c0006 | 1 | NA18950.hp2 | synonymous_variant | LOW | c.2400T>C | p.Tyr800Tyr | FAM120C | ENSG00000184083.12 | transcript | ENST00000375180.7 | protein_coding | 11/16 | 2456/8056 | 2400/3291 | 800/1096 | chrX | 54091339 | ||
chrX:54182860
|
C | G | 1 | a0001c0005 | 1 | NA18959.hp1 | synonymous_variant | LOW | c.339G>C | p.Leu113Leu | FAM120C | ENSG00000184083.12 | transcript | ENST00000375180.7 | protein_coding | 1/16 | 395/8056 | 339/3291 | 113/1096 | chrX | 54182860 |
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:54068326
|
AT | A | 1 | a0001c0001t0070 | 1 | NA19091.hp1 | 3_prime_UTR_variant | MODIFIER | c.*4706delA | FAM120C | ENSG00000184083.12 | transcript | ENST00000375180.7 | protein_coding | 16/16 | 4706 | chrX | 54068326 | |||||
chrX:54068334
|
A | AT | 1 | a0001c0001t0073 | 1 | NA19078.hp1 | 3_prime_UTR_variant | MODIFIER | c.*4698dupA | FAM120C | ENSG00000184083.12 | transcript | ENST00000375180.7 | protein_coding | 16/16 | 4698 | chrX | 54068334 | |||||
chrX:54068334
|
AT | A | 1 | a0001c0001t0070 | 1 | NA19091.hp1 | 3_prime_UTR_variant | MODIFIER | c.*4698delA | FAM120C | ENSG00000184083.12 | transcript | ENST00000375180.7 | protein_coding | 16/16 | 4698 | chrX | 54068334 | |||||
chrX:54068394
|
TA | T | 1 | a0001c0001t0070 | 1 | NA19091.hp1 | 3_prime_UTR_variant | MODIFIER | c.*4638delT | FAM120C | ENSG00000184083.12 | transcript | ENST00000375180.7 | protein_coding | 16/16 | 4638 | chrX | 54068394 | |||||
chrX:54068462
|
CT | C | 1 | a0001c0001t0070 | 1 | NA19091.hp1 | 3_prime_UTR_variant | MODIFIER | c.*4570delA | FAM120C | ENSG00000184083.12 | transcript | ENST00000375180.7 | protein_coding | 16/16 | 4570 | chrX | 54068462 | |||||
chrX:54068517
|
T | TA | 1 | a0005c0007t0034 | 1 | NA19075.hp1 | 3_prime_UTR_variant | MODIFIER | c.*4515dupT | FAM120C | ENSG00000184083.12 | transcript | ENST00000375180.7 | protein_coding | 16/16 | 4515 | chrX | 54068517 | |||||
chrX:54068529
|
C | CT | 1 | a0005c0007t0034 | 1 | NA19075.hp1 | 3_prime_UTR_variant | MODIFIER | c.*4503dupA | FAM120C | ENSG00000184083.12 | transcript | ENST00000375180.7 | protein_coding | 16/16 | 4503 | chrX | 54068529 | |||||
chrX:54068557
|
AG | A | 1 | a0001c0001t0070 | 1 | NA19091.hp1 | 3_prime_UTR_variant | MODIFIER | c.*4475delC | FAM120C | ENSG00000184083.12 | transcript | ENST00000375180.7 | protein_coding | 16/16 | 4475 | chrX | 54068557 | |||||
chrX:54068565
|
TG | T | 1 | a0001c0001t0070 | 1 | NA19091.hp1 | 3_prime_UTR_variant | MODIFIER | c.*4467delC | FAM120C | ENSG00000184083.12 | transcript | ENST00000375180.7 | protein_coding | 16/16 | 4467 | chrX | 54068565 | |||||
chrX:54068652
|
GA | G | 2 | a0001c0001t0070a0005c0007t0034 | 2 | NA19075.hp1 NA19091.hp1 |
3_prime_UTR_variant | MODIFIER | c.*4380delT | FAM120C | ENSG00000184083.12 | transcript | ENST00000375180.7 | protein_coding | 16/16 | 4380 | chrX | 54068652 | |||||
chrX:54068701
|
C | CAG | 1 | a0005c0007t0034 | 1 | NA19075.hp1 | 3_prime_UTR_variant | MODIFIER | c.*4330_*4331dupCT | FAM120C | ENSG00000184083.12 | transcript | ENST00000375180.7 | protein_coding | 16/16 | 4331 | chrX | 54068701 | |||||
chrX:54068710
|
C | CA | 1 | a0005c0007t0034 | 1 | NA19075.hp1 | 3_prime_UTR_variant | MODIFIER | c.*4322_*4323insT | FAM120C | ENSG00000184083.12 | transcript | ENST00000375180.7 | protein_coding | 16/16 | 4322 | chrX | 54068710 | |||||
chrX:54068711
|
TA | T | 1 | a0001c0001t0073 | 1 | NA19078.hp1 | 3_prime_UTR_variant | MODIFIER | c.*4321delT | FAM120C | ENSG00000184083.12 | transcript | ENST00000375180.7 | protein_coding | 16/16 | 4321 | chrX | 54068711 | |||||
chrX:54068784
|
T | TAGAAC | 13 | a0001c0001t0007a0001c0001t0009a0001c0001t0019others(10): Show | 24 | HG00735.hp2 HG00738.hp1 HG01069.hp1 others(21): Show |
3_prime_UTR_variant | MODIFIER | c.*4244_*4248dupGTTC others(1): Show |
FAM120C | ENSG00000184083.12 | transcript | ENST00000375180.7 | protein_coding | 16/16 | 4248 | chrX | 54068784 | |||||
chrX:54068789
|
C | CAGAACAG others(3): Show |
8 | a0001c0001t0013a0001c0001t0015a0001c0001t0025others(5): Show | 14 | HG01169.hp2 HG01884.hp1 HG02071.hp1 others(11): Show |
3_prime_UTR_variant | MODIFIER | c.*4243_*4244insATTC others(6): Show |
FAM120C | ENSG00000184083.12 | transcript | ENST00000375180.7 | protein_coding | 16/16 | 4243 | chrX | 54068789 | |||||
chrX:54068789
|
C | CAGAACAG others(8): Show |
2 | a0001c0001t0022a0001c0001t0041 | 4 | HG01243.hp1 HG02717.hp1 HG03516.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*4243_*4244insATTC others(11): Show |
FAM120C | ENSG00000184083.12 | transcript | ENST00000375180.7 | protein_coding | 16/16 | 4243 | chrX | 54068789 | |||||
chrX:54068789
|
C | CAGAAT | 3 | a0001c0001t0030a0001c0001t0042a0001c0001t0072 | 4 | HG01884.hp2 HG02615.hp2 HG02809.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*4239_*4243dupATTC others(1): Show |
FAM120C | ENSG00000184083.12 | transcript | ENST00000375180.7 | protein_coding | 16/16 | 4243 | chrX | 54068789 | |||||
chrX:54068789
|
C | CAGAATAG others(3): Show |
3 | a0001c0001t0018a0001c0001t0039a0001c0001t0054 | 5 | HG02809.hp2 HG03130.hp1 HG06807.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*4234_*4243dupATTC others(6): Show |
FAM120C | ENSG00000184083.12 | transcript | ENST00000375180.7 | protein_coding | 16/16 | 4243 | chrX | 54068789 | |||||
chrX:54068789
|
C | CAGAATAG others(8): Show |
1 | a0001c0001t0033 | 2 | HG02559.hp2 HG02647.hp1 |
3_prime_UTR_variant | MODIFIER | c.*4229_*4243dupATTC others(11): Show |
FAM120C | ENSG00000184083.12 | transcript | ENST00000375180.7 | protein_coding | 16/16 | 4243 | chrX | 54068789 | |||||
chrX:54068789
|
C | T | 1 | a0001c0001t0067 | 1 | HG02257.hp1 | 3_prime_UTR_variant | MODIFIER | c.*4244G>A | FAM120C | ENSG00000184083.12 | transcript | ENST00000375180.7 | protein_coding | 16/16 | 4244 | chrX | 54068789 | |||||
chrX:54068789
|
CAGAAT | C | 7 | a0001c0001t0016a0001c0001t0023a0001c0001t0029others(4): Show | 13 | HG00140.hp1 HG00642.hp1 HG01358.hp1 others(10): Show |
3_prime_UTR_variant | MODIFIER | c.*4239_*4243delATTC others(1): Show |
FAM120C | ENSG00000184083.12 | transcript | ENST00000375180.7 | protein_coding | 16/16 | 4239 | chrX | 54068789 | |||||
chrX:54068789
|
CAGAATAG others(3): Show |
C | 12 | a0001c0001t0003a0001c0001t0011a0001c0001t0012others(9): Show | 31 | HG01070.hp2 HG01074.hp1 HG01106.hp1 others(28): Show |
3_prime_UTR_variant | MODIFIER | c.*4234_*4243delATTC others(6): Show |
FAM120C | ENSG00000184083.12 | transcript | ENST00000375180.7 | protein_coding | 16/16 | 4234 | chrX | 54068789 | |||||
chrX:54068789
|
CAGAATAG others(8): Show |
C | 6 | a0001c0001t0002a0001c0001t0008a0001c0001t0017others(3): Show | 26 | HG00558.hp2 HG00609.hp1 HG00621.hp1 others(23): Show |
3_prime_UTR_variant | MODIFIER | c.*4229_*4243delATTC others(11): Show |
FAM120C | ENSG00000184083.12 | transcript | ENST00000375180.7 | protein_coding | 16/16 | 4229 | chrX | 54068789 | |||||
chrX:54068789
|
CAGAATAG others(13): Show |
C | 1 | a0001c0001t0032 | 2 | NA18972.hp1 NA18973.hp1 |
3_prime_UTR_variant | MODIFIER | c.*4224_*4243delATTC others(16): Show |
FAM120C | ENSG00000184083.12 | transcript | ENST00000375180.7 | protein_coding | 16/16 | 4224 | chrX | 54068789 | |||||
chrX:54068789
|
CAGAATAG others(18): Show |
C | 1 | a0007c0004t0051 | 1 | HG03453.hp1 | 3_prime_UTR_variant | MODIFIER | c.*4219_*4243delATTC others(21): Show |
FAM120C | ENSG00000184083.12 | transcript | ENST00000375180.7 | protein_coding | 16/16 | 4219 | chrX | 54068789 | |||||
chrX:54068794
|
T | C | 25 | a0001c0001t0001a0001c0001t0004a0001c0001t0005others(22): Show | 63 | HG00280.hp1 HG00558.hp1 HG00673.hp1 others(60): Show |
3_prime_UTR_variant | MODIFIER | c.*4239A>G | FAM120C | ENSG00000184083.12 | transcript | ENST00000375180.7 | protein_coding | 16/16 | 4239 | chrX | 54068794 | |||||
chrX:54068799
|
T | C | 14 | a0001c0001t0007a0001c0001t0009a0001c0001t0023others(11): Show | 26 | HG00140.hp1 HG00642.hp1 HG01069.hp1 others(23): Show |
3_prime_UTR_variant | MODIFIER | c.*4234A>G | FAM120C | ENSG00000184083.12 | transcript | ENST00000375180.7 | protein_coding | 16/16 | 4234 | chrX | 54068799 | |||||
chrX:54068804
|
T | C | 29 | a0001c0001t0001a0001c0001t0003a0001c0001t0004others(26): Show | 81 | HG00280.hp1 HG00558.hp1 HG00673.hp1 others(78): Show |
3_prime_UTR_variant | MODIFIER | c.*4229A>G | FAM120C | ENSG00000184083.12 | transcript | ENST00000375180.7 | protein_coding | 16/16 | 4229 | chrX | 54068804 | |||||
chrX:54068809
|
T | C | 4 | a0001c0001t0023a0001c0001t0029a0001c0001t0062others(1): Show | 7 | HG00140.hp1 HG00642.hp1 HG01358.hp1 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*4224A>G | FAM120C | ENSG00000184083.12 | transcript | ENST00000375180.7 | protein_coding | 16/16 | 4224 | chrX | 54068809 | |||||
chrX:54068814
|
T | C | 7 | a0001c0001t0003a0001c0001t0012a0001c0001t0014others(4): Show | 22 | HG01106.hp1 HG01256.hp1 HG01433.hp1 others(19): Show |
3_prime_UTR_variant | MODIFIER | c.*4219A>G | FAM120C | ENSG00000184083.12 | transcript | ENST00000375180.7 | protein_coding | 16/16 | 4219 | chrX | 54068814 | |||||
chrX:54068856
|
G | A | 1 | a0001c0001t0037 | 1 | NA18965.hp1 | 3_prime_UTR_variant | MODIFIER | c.*4177C>T | FAM120C | ENSG00000184083.12 | transcript | ENST00000375180.7 | protein_coding | 16/16 | 4177 | chrX | 54068856 | |||||
chrX:54068870
|
TG | T | 2 | a0001c0001t0070a0005c0007t0034 | 2 | NA19075.hp1 NA19091.hp1 |
3_prime_UTR_variant | MODIFIER | c.*4162delC | FAM120C | ENSG00000184083.12 | transcript | ENST00000375180.7 | protein_coding | 16/16 | 4162 | chrX | 54068870 | |||||
chrX:54068905
|
T | TG | 1 | a0001c0001t0070 | 1 | NA19091.hp1 | 3_prime_UTR_variant | MODIFIER | c.*4127dupC | FAM120C | ENSG00000184083.12 | transcript | ENST00000375180.7 | protein_coding | 16/16 | 4127 | chrX | 54068905 | |||||
chrX:54068908
|
G | A | 1 | a0001c0001t0045 | 1 | HG03471.hp1 | 3_prime_UTR_variant | MODIFIER | c.*4125C>T | FAM120C | ENSG00000184083.12 | transcript | ENST00000375180.7 | protein_coding | 16/16 | 4125 | chrX | 54068908 | |||||
chrX:54068918
|
AT | A | 1 | a0005c0007t0034 | 1 | NA19075.hp1 | 3_prime_UTR_variant | MODIFIER | c.*4114delA | FAM120C | ENSG00000184083.12 | transcript | ENST00000375180.7 | protein_coding | 16/16 | 4114 | chrX | 54068918 | |||||
chrX:54068990
|
C | T | 1 | a0001c0001t0067 | 1 | HG02257.hp1 | 3_prime_UTR_variant | MODIFIER | c.*4043G>A | FAM120C | ENSG00000184083.12 | transcript | ENST00000375180.7 | protein_coding | 16/16 | 4043 | chrX | 54068990 | |||||
chrX:54068994
|
CA | C | 1 | a0001c0001t0070 | 1 | NA19091.hp1 | 3_prime_UTR_variant | MODIFIER | c.*4038delT | FAM120C | ENSG00000184083.12 | transcript | ENST00000375180.7 | protein_coding | 16/16 | 4038 | chrX | 54068994 | |||||
chrX:54069061
|
AT | A | 1 | a0001c0001t0070 | 1 | NA19091.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3971delA | FAM120C | ENSG00000184083.12 | transcript | ENST00000375180.7 | protein_coding | 16/16 | 3971 | chrX | 54069061 | |||||
chrX:54069172
|
G | T | 1 | a0001c0001t0070 | 1 | NA19091.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3861C>A | FAM120C | ENSG00000184083.12 | transcript | ENST00000375180.7 | protein_coding | 16/16 | 3861 | chrX | 54069172 | |||||
chrX:54069183
|
G | GC | 1 | a0001c0001t0070 | 1 | NA19091.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3849dupG | FAM120C | ENSG00000184083.12 | transcript | ENST00000375180.7 | protein_coding | 16/16 | 3849 | chrX | 54069183 | |||||
chrX:54069186
|
C | CT | 1 | a0005c0007t0034 | 1 | NA19075.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3846dupA | FAM120C | ENSG00000184083.12 | transcript | ENST00000375180.7 | protein_coding | 16/16 | 3846 | chrX | 54069186 | |||||
chrX:54069237
|
A | G | 1 | a0001c0001t0070 | 1 | NA19091.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3796T>C | FAM120C | ENSG00000184083.12 | transcript | ENST00000375180.7 | protein_coding | 16/16 | 3796 | chrX | 54069237 | |||||
chrX:54069319
|
A | AC | 1 | a0001c0001t0070 | 1 | NA19091.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3713dupG | FAM120C | ENSG00000184083.12 | transcript | ENST00000375180.7 | protein_coding | 16/16 | 3713 | chrX | 54069319 | |||||
chrX:54069401
|
T | TTA | 1 | a0001c0001t0070 | 1 | NA19091.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3631_*3632insTA | FAM120C | ENSG00000184083.12 | transcript | ENST00000375180.7 | protein_coding | 16/16 | 3631 | chrX | 54069401 | |||||
chrX:54069402
|
A | C | 1 | a0001c0001t0070 | 1 | NA19091.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3631T>G | FAM120C | ENSG00000184083.12 | transcript | ENST00000375180.7 | protein_coding | 16/16 | 3631 | chrX | 54069402 | |||||
chrX:54069402
|
AT | A | 1 | a0005c0007t0034 | 1 | NA19075.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3630delA | FAM120C | ENSG00000184083.12 | transcript | ENST00000375180.7 | protein_coding | 16/16 | 3630 | chrX | 54069402 | |||||
chrX:54069412
|
C | CT | 1 | a0005c0007t0034 | 1 | NA19075.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3620dupA | FAM120C | ENSG00000184083.12 | transcript | ENST00000375180.7 | protein_coding | 16/16 | 3620 | chrX | 54069412 | |||||
chrX:54069415
|
T | A | 1 | a0001c0001t0070 | 1 | NA19091.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3618A>T | FAM120C | ENSG00000184083.12 | transcript | ENST00000375180.7 | protein_coding | 16/16 | 3618 | chrX | 54069415 | |||||
chrX:54069456
|
G | GTC | 1 | a0001c0001t0070 | 1 | NA19091.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3576_*3577insGA | FAM120C | ENSG00000184083.12 | transcript | ENST00000375180.7 | protein_coding | 16/16 | 3576 | chrX | 54069456 | |||||
chrX:54069458
|
TC | T | 1 | a0001c0001t0070 | 1 | NA19091.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3574delG | FAM120C | ENSG00000184083.12 | transcript | ENST00000375180.7 | protein_coding | 16/16 | 3574 | chrX | 54069458 | |||||
chrX:54069460
|
GT | G | 1 | a0005c0007t0034 | 1 | NA19075.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3572delA | FAM120C | ENSG00000184083.12 | transcript | ENST00000375180.7 | protein_coding | 16/16 | 3572 | chrX | 54069460 | |||||
chrX:54069492
|
A | AC | 1 | a0005c0007t0034 | 1 | NA19075.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3540dupG | FAM120C | ENSG00000184083.12 | transcript | ENST00000375180.7 | protein_coding | 16/16 | 3540 | chrX | 54069492 | |||||
chrX:54069642
|
C | CA | 1 | a0005c0007t0034 | 1 | NA19075.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3390dupT | FAM120C | ENSG00000184083.12 | transcript | ENST00000375180.7 | protein_coding | 16/16 | 3390 | chrX | 54069642 | |||||
chrX:54069680
|
A | G | 1 | a0001c0001t0025 | 2 | HG02630.hp2 HG02895.hp1 |
3_prime_UTR_variant | MODIFIER | c.*3353T>C | FAM120C | ENSG00000184083.12 | transcript | ENST00000375180.7 | protein_coding | 16/16 | 3353 | chrX | 54069680 | |||||
chrX:54069728
|
AT | A | 1 | a0001c0001t0070 | 1 | NA19091.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3304delA | FAM120C | ENSG00000184083.12 | transcript | ENST00000375180.7 | protein_coding | 16/16 | 3304 | chrX | 54069728 | |||||
chrX:54069767
|
C | CA | 1 | a0001c0001t0070 | 1 | NA19091.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3265dupT | FAM120C | ENSG00000184083.12 | transcript | ENST00000375180.7 | protein_coding | 16/16 | 3265 | chrX | 54069767 | |||||
chrX:54069866
|
TC | T | 1 | a0001c0001t0070 | 1 | NA19091.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3166delG | FAM120C | ENSG00000184083.12 | transcript | ENST00000375180.7 | protein_coding | 16/16 | 3166 | chrX | 54069866 | |||||
chrX:54069938
|
T | TG | 1 | a0001c0001t0070 | 1 | NA19091.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3094dupC | FAM120C | ENSG00000184083.12 | transcript | ENST00000375180.7 | protein_coding | 16/16 | 3094 | chrX | 54069938 | |||||
chrX:54069965
|
T | TC | 1 | a0005c0007t0034 | 1 | NA19075.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3067dupG | FAM120C | ENSG00000184083.12 | transcript | ENST00000375180.7 | protein_coding | 16/16 | 3067 | chrX | 54069965 | |||||
chrX:54069967
|
AT | A | 1 | a0001c0001t0070 | 1 | NA19091.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3065delA | FAM120C | ENSG00000184083.12 | transcript | ENST00000375180.7 | protein_coding | 16/16 | 3065 | chrX | 54069967 | |||||
chrX:54070019
|
G | GA | 1 | a0001c0001t0070 | 1 | NA19091.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3013dupT | FAM120C | ENSG00000184083.12 | transcript | ENST00000375180.7 | protein_coding | 16/16 | 3013 | chrX | 54070019 | |||||
chrX:54070059
|
G | GT | 1 | a0001c0001t0070 | 1 | NA19091.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2973_*2974insA | FAM120C | ENSG00000184083.12 | transcript | ENST00000375180.7 | protein_coding | 16/16 | 2973 | chrX | 54070059 | |||||
chrX:54070076
|
AC | A | 1 | a0001c0001t0070 | 1 | NA19091.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2956delG | FAM120C | ENSG00000184083.12 | transcript | ENST00000375180.7 | protein_coding | 16/16 | 2956 | chrX | 54070076 | |||||
chrX:54070095
|
G | GT | 1 | a0001c0001t0070 | 1 | NA19091.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2937dupA | FAM120C | ENSG00000184083.12 | transcript | ENST00000375180.7 | protein_coding | 16/16 | 2937 | chrX | 54070095 | |||||
chrX:54070107
|
GA | G | 1 | a0001c0001t0070 | 1 | NA19091.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2925delT | FAM120C | ENSG00000184083.12 | transcript | ENST00000375180.7 | protein_coding | 16/16 | 2925 | chrX | 54070107 | |||||
chrX:54070130
|
GA | G | 1 | a0005c0007t0034 | 1 | NA19075.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2902delT | FAM120C | ENSG00000184083.12 | transcript | ENST00000375180.7 | protein_coding | 16/16 | 2902 | chrX | 54070130 | |||||
chrX:54070158
|
G | GT | 1 | a0001c0001t0070 | 1 | NA19091.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2874dupA | FAM120C | ENSG00000184083.12 | transcript | ENST00000375180.7 | protein_coding | 16/16 | 2874 | chrX | 54070158 | |||||
chrX:54070162
|
AT | A | 1 | a0005c0007t0034 | 1 | NA19075.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2870delA | FAM120C | ENSG00000184083.12 | transcript | ENST00000375180.7 | protein_coding | 16/16 | 2870 | chrX | 54070162 | |||||
chrX:54070177
|
T | TA | 1 | a0001c0001t0070 | 1 | NA19091.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2855dupT | FAM120C | ENSG00000184083.12 | transcript | ENST00000375180.7 | protein_coding | 16/16 | 2855 | chrX | 54070177 | |||||
chrX:54070242
|
TC | T | 1 | a0001c0001t0070 | 1 | NA19091.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2790delG | FAM120C | ENSG00000184083.12 | transcript | ENST00000375180.7 | protein_coding | 16/16 | 2790 | chrX | 54070242 | |||||
chrX:54070244
|
C | CA | 1 | a0005c0007t0034 | 1 | NA19075.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2788dupT | FAM120C | ENSG00000184083.12 | transcript | ENST00000375180.7 | protein_coding | 16/16 | 2788 | chrX | 54070244 | |||||
chrX:54070261
|
T | TG | 1 | a0001c0001t0070 | 1 | NA19091.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2771dupC | FAM120C | ENSG00000184083.12 | transcript | ENST00000375180.7 | protein_coding | 16/16 | 2771 | chrX | 54070261 | |||||
chrX:54070282
|
AC | A | 1 | a0001c0001t0070 | 1 | NA19091.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2750delG | FAM120C | ENSG00000184083.12 | transcript | ENST00000375180.7 | protein_coding | 16/16 | 2750 | chrX | 54070282 | |||||
chrX:54070313
|
A | AG | 1 | a0001c0001t0070 | 1 | NA19091.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2719dupC | FAM120C | ENSG00000184083.12 | transcript | ENST00000375180.7 | protein_coding | 16/16 | 2719 | chrX | 54070313 | |||||
chrX:54070326
|
GT | G | 1 | a0001c0001t0070 | 1 | NA19091.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2706delA | FAM120C | ENSG00000184083.12 | transcript | ENST00000375180.7 | protein_coding | 16/16 | 2706 | chrX | 54070326 | |||||
chrX:54070346
|
AC | A | 1 | a0005c0007t0034 | 1 | NA19075.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2686delG | FAM120C | ENSG00000184083.12 | transcript | ENST00000375180.7 | protein_coding | 16/16 | 2686 | chrX | 54070346 | |||||
chrX:54070360
|
C | A | 1 | a0001c0001t0052 | 1 | HG00738.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2673G>T | FAM120C | ENSG00000184083.12 | transcript | ENST00000375180.7 | protein_coding | 16/16 | 2673 | chrX | 54070360 | |||||
chrX:54070411
|
G | GT | 1 | a0005c0007t0034 | 1 | NA19075.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2621dupA | FAM120C | ENSG00000184083.12 | transcript | ENST00000375180.7 | protein_coding | 16/16 | 2621 | chrX | 54070411 | |||||
chrX:54070432
|
T | TC | 1 | a0001c0001t0070 | 1 | NA19091.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2600dupG | FAM120C | ENSG00000184083.12 | transcript | ENST00000375180.7 | protein_coding | 16/16 | 2600 | chrX | 54070432 | |||||
chrX:54070536
|
T | C | 2 | a0001c0001t0059a0001c0001t0069 | 2 | HG03017.hp1 NA20905.hp1 |
3_prime_UTR_variant | MODIFIER | c.*2497A>G | FAM120C | ENSG00000184083.12 | transcript | ENST00000375180.7 | protein_coding | 16/16 | 2497 | chrX | 54070536 | |||||
chrX:54070578
|
CCA | C | 1 | a0001c0001t0070 | 1 | NA19091.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2453_*2454delTG | FAM120C | ENSG00000184083.12 | transcript | ENST00000375180.7 | protein_coding | 16/16 | 2453 | chrX | 54070578 | |||||
chrX:54070613
|
AAT | A | 1 | a0001c0001t0070 | 1 | NA19091.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2418_*2419delAT | FAM120C | ENSG00000184083.12 | transcript | ENST00000375180.7 | protein_coding | 16/16 | 2418 | chrX | 54070613 | |||||
chrX:54070616
|
TC | T | 1 | a0005c0007t0034 | 1 | NA19075.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2416delG | FAM120C | ENSG00000184083.12 | transcript | ENST00000375180.7 | protein_coding | 16/16 | 2416 | chrX | 54070616 | |||||
chrX:54070617
|
C | T | 1 | a0001c0001t0070 | 1 | NA19091.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2416G>A | FAM120C | ENSG00000184083.12 | transcript | ENST00000375180.7 | protein_coding | 16/16 | 2416 | chrX | 54070617 | |||||
chrX:54070646
|
TC | T | 2 | a0001c0001t0070a0005c0007t0034 | 2 | NA19075.hp1 NA19091.hp1 |
3_prime_UTR_variant | MODIFIER | c.*2386delG | FAM120C | ENSG00000184083.12 | transcript | ENST00000375180.7 | protein_coding | 16/16 | 2386 | chrX | 54070646 | |||||
chrX:54070678
|
G | GA | 1 | a0001c0001t0070 | 1 | NA19091.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2354dupT | FAM120C | ENSG00000184083.12 | transcript | ENST00000375180.7 | protein_coding | 16/16 | 2354 | chrX | 54070678 | |||||
chrX:54070691
|
G | GAT | 1 | a0001c0001t0070 | 1 | NA19091.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2341_*2342insAT | FAM120C | ENSG00000184083.12 | transcript | ENST00000375180.7 | protein_coding | 16/16 | 2341 | chrX | 54070691 | |||||
chrX:54070693
|
T | G | 1 | a0001c0001t0070 | 1 | NA19091.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2340A>C | FAM120C | ENSG00000184083.12 | transcript | ENST00000375180.7 | protein_coding | 16/16 | 2340 | chrX | 54070693 | |||||
chrX:54070736
|
TC | T | 1 | a0001c0001t0070 | 1 | NA19091.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2296delG | FAM120C | ENSG00000184083.12 | transcript | ENST00000375180.7 | protein_coding | 16/16 | 2296 | chrX | 54070736 | |||||
chrX:54070800
|
A | AT | 1 | a0005c0007t0034 | 1 | NA19075.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2232dupA | FAM120C | ENSG00000184083.12 | transcript | ENST00000375180.7 | protein_coding | 16/16 | 2232 | chrX | 54070800 | |||||
chrX:54070857
|
C | G | 1 | a0001c0001t0070 | 1 | NA19091.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2176G>C | FAM120C | ENSG00000184083.12 | transcript | ENST00000375180.7 | protein_coding | 16/16 | 2176 | chrX | 54070857 | |||||
chrX:54070860
|
TC | T | 1 | a0005c0007t0034 | 1 | NA19075.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2172delG | FAM120C | ENSG00000184083.12 | transcript | ENST00000375180.7 | protein_coding | 16/16 | 2172 | chrX | 54070860 | |||||
chrX:54070922
|
G | GT | 1 | a0005c0007t0034 | 1 | NA19075.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2110dupA | FAM120C | ENSG00000184083.12 | transcript | ENST00000375180.7 | protein_coding | 16/16 | 2110 | chrX | 54070922 | |||||
chrX:54071013
|
T | TG | 1 | a0001c0001t0070 | 1 | NA19091.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2019dupC | FAM120C | ENSG00000184083.12 | transcript | ENST00000375180.7 | protein_coding | 16/16 | 2019 | chrX | 54071013 | |||||
chrX:54071037
|
CA | C | 1 | a0001c0001t0070 | 1 | NA19091.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1995delT | FAM120C | ENSG00000184083.12 | transcript | ENST00000375180.7 | protein_coding | 16/16 | 1995 | chrX | 54071037 | |||||
chrX:54071077
|
G | GA | 1 | a0001c0001t0070 | 1 | NA19091.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1955_*1956insT | FAM120C | ENSG00000184083.12 | transcript | ENST00000375180.7 | protein_coding | 16/16 | 1955 | chrX | 54071077 | |||||
chrX:54071086
|
GT | G | 1 | a0001c0001t0070 | 1 | NA19091.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1946delA | FAM120C | ENSG00000184083.12 | transcript | ENST00000375180.7 | protein_coding | 16/16 | 1946 | chrX | 54071086 | |||||
chrX:54071240
|
G | GT | 1 | a0001c0001t0070 | 1 | NA19091.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1792dupA | FAM120C | ENSG00000184083.12 | transcript | ENST00000375180.7 | protein_coding | 16/16 | 1792 | chrX | 54071240 | |||||
chrX:54071320
|
CT | C | 1 | a0001c0001t0070 | 1 | NA19091.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1712delA | FAM120C | ENSG00000184083.12 | transcript | ENST00000375180.7 | protein_coding | 16/16 | 1712 | chrX | 54071320 | |||||
chrX:54071478
|
TC | T | 1 | a0005c0007t0034 | 1 | NA19075.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1554delG | FAM120C | ENSG00000184083.12 | transcript | ENST00000375180.7 | protein_coding | 16/16 | 1554 | chrX | 54071478 | |||||
chrX:54071487
|
A | G | 2 | a0001c0001t0053a0002c0002t0047 | 2 | HG00642.hp1 HG00735.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1546T>C | FAM120C | ENSG00000184083.12 | transcript | ENST00000375180.7 | protein_coding | 16/16 | 1546 | chrX | 54071487 | |||||
chrX:54071541
|
G | GA | 1 | a0005c0007t0034 | 1 | NA19075.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1491dupT | FAM120C | ENSG00000184083.12 | transcript | ENST00000375180.7 | protein_coding | 16/16 | 1491 | chrX | 54071541 | |||||
chrX:54071570
|
CA | C | 1 | a0005c0007t0034 | 1 | NA19075.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1462delT | FAM120C | ENSG00000184083.12 | transcript | ENST00000375180.7 | protein_coding | 16/16 | 1462 | chrX | 54071570 | |||||
chrX:54071611
|
T | TC | 1 | a0001c0001t0073 | 1 | NA19078.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1421dupG | FAM120C | ENSG00000184083.12 | transcript | ENST00000375180.7 | protein_coding | 16/16 | 1421 | chrX | 54071611 | |||||
chrX:54071646
|
G | GC | 1 | a0001c0001t0070 | 1 | NA19091.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1386dupG | FAM120C | ENSG00000184083.12 | transcript | ENST00000375180.7 | protein_coding | 16/16 | 1386 | chrX | 54071646 | |||||
chrX:54071656
|
TC | T | 1 | a0005c0007t0034 | 1 | NA19075.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1376delG | FAM120C | ENSG00000184083.12 | transcript | ENST00000375180.7 | protein_coding | 16/16 | 1376 | chrX | 54071656 | |||||
chrX:54071841
|
A | AT | 1 | a0005c0007t0034 | 1 | NA19075.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1191dupA | FAM120C | ENSG00000184083.12 | transcript | ENST00000375180.7 | protein_coding | 16/16 | 1191 | chrX | 54071841 | |||||
chrX:54071933
|
CATGT | C | 81 | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(78): Show | 189 | HG00140.hp1 HG00280.hp1 HG00558.hp1 others(186): Show |
3_prime_UTR_variant | MODIFIER | c.*1096_*1099delACAT | FAM120C | ENSG00000184083.12 | transcript | ENST00000375180.7 | protein_coding | 16/16 | 1096 | chrX | 54071933 | |||||
chrX:54071948
|
G | A | 1 | a0001c0001t0064 | 1 | HG02074.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1085C>T | FAM120C | ENSG00000184083.12 | transcript | ENST00000375180.7 | protein_coding | 16/16 | 1085 | chrX | 54071948 | |||||
chrX:54071966
|
A | G | 1 | a0001c0001t0046 | 1 | HG02129.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1067T>C | FAM120C | ENSG00000184083.12 | transcript | ENST00000375180.7 | protein_coding | 16/16 | 1067 | chrX | 54071966 | |||||
chrX:54071995
|
T | C | 1 | a0005c0007t0034 | 1 | NA19075.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1038A>G | FAM120C | ENSG00000184083.12 | transcript | ENST00000375180.7 | protein_coding | 16/16 | 1038 | chrX | 54071995 | |||||
chrX:54071999
|
CA | C | 1 | a0005c0007t0034 | 1 | NA19075.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1033delT | FAM120C | ENSG00000184083.12 | transcript | ENST00000375180.7 | protein_coding | 16/16 | 1033 | chrX | 54071999 | |||||
chrX:54072001
|
C | T | 1 | a0005c0007t0034 | 1 | NA19075.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1032G>A | FAM120C | ENSG00000184083.12 | transcript | ENST00000375180.7 | protein_coding | 16/16 | 1032 | chrX | 54072001 | |||||
chrX:54072010
|
A | AC | 1 | a0001c0001t0074 | 1 | HG00609.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1022dupG | FAM120C | ENSG00000184083.12 | transcript | ENST00000375180.7 | protein_coding | 16/16 | 1022 | chrX | 54072010 | |||||
chrX:54072084
|
G | GT | 1 | a0005c0007t0034 | 1 | NA19075.hp1 | 3_prime_UTR_variant | MODIFIER | c.*948dupA | FAM120C | ENSG00000184083.12 | transcript | ENST00000375180.7 | protein_coding | 16/16 | 948 | chrX | 54072084 | |||||
chrX:54072089
|
T | TG | 1 | a0005c0007t0034 | 1 | NA19075.hp1 | 3_prime_UTR_variant | MODIFIER | c.*943dupC | FAM120C | ENSG00000184083.12 | transcript | ENST00000375180.7 | protein_coding | 16/16 | 943 | chrX | 54072089 | |||||
chrX:54072159
|
T | TCA | 11 | a0001c0001t0007a0001c0001t0013a0001c0001t0014others(8): Show | 26 | HG00735.hp2 HG01192.hp1 HG01256.hp1 others(23): Show |
3_prime_UTR_variant | MODIFIER | c.*872_*873dupTG | FAM120C | ENSG00000184083.12 | transcript | ENST00000375180.7 | protein_coding | 16/16 | 873 | chrX | 54072159 | |||||
chrX:54072159
|
T | TCACA | 18 | a0001c0001t0004a0001c0001t0008a0001c0001t0011others(15): Show | 47 | HG00621.hp1 HG00642.hp1 HG00738.hp1 others(44): Show |
3_prime_UTR_variant | MODIFIER | c.*870_*873dupTGTG | FAM120C | ENSG00000184083.12 | transcript | ENST00000375180.7 | protein_coding | 16/16 | 873 | chrX | 54072159 | |||||
chrX:54072159
|
T | TCACACA | 22 | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(19): Show | 65 | HG00140.hp1 HG00280.hp1 HG00558.hp2 others(62): Show |
3_prime_UTR_variant | MODIFIER | c.*868_*873dupTGTGTG | FAM120C | ENSG00000184083.12 | transcript | ENST00000375180.7 | protein_coding | 16/16 | 873 | chrX | 54072159 | |||||
chrX:54072159
|
T | TCACACAC others(1): Show |
8 | a0001c0001t0005a0001c0001t0017a0001c0001t0060others(5): Show | 17 | HG00558.hp1 HG01167.hp1 HG01169.hp1 others(14): Show |
3_prime_UTR_variant | MODIFIER | c.*866_*873dupTGTGTG others(2): Show |
FAM120C | ENSG00000184083.12 | transcript | ENST00000375180.7 | protein_coding | 16/16 | 873 | chrX | 54072159 | |||||
chrX:54072159
|
T | TCACACAC others(3): Show |
3 | a0001c0001t0010a0001c0001t0065a0001c0001t0066 | 8 | HG02135.hp1 NA18612.hp1 NA18967.hp1 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*864_*873dupTGTGTG others(4): Show |
FAM120C | ENSG00000184083.12 | transcript | ENST00000375180.7 | protein_coding | 16/16 | 873 | chrX | 54072159 | |||||
chrX:54072159
|
T | TCACACAC others(5): Show |
2 | a0001c0001t0067a0001c0001t0068 | 2 | HG02257.hp1 HG04204.hp1 |
3_prime_UTR_variant | MODIFIER | c.*862_*873dupTGTGTG others(6): Show |
FAM120C | ENSG00000184083.12 | transcript | ENST00000375180.7 | protein_coding | 16/16 | 873 | chrX | 54072159 | |||||
chrX:54072159
|
TCA | T | 1 | a0001c0001t0035 | 1 | NA18972.hp2 | 3_prime_UTR_variant | MODIFIER | c.*872_*873delTG | FAM120C | ENSG00000184083.12 | transcript | ENST00000375180.7 | protein_coding | 16/16 | 872 | chrX | 54072159 | |||||
chrX:54072159
|
TCACA | T | 1 | a0001c0001t0039 | 1 | NA18906.hp2 | 3_prime_UTR_variant | MODIFIER | c.*870_*873delTGTG | FAM120C | ENSG00000184083.12 | transcript | ENST00000375180.7 | protein_coding | 16/16 | 870 | chrX | 54072159 | |||||
chrX:54072159
|
TCACACA | T | 2 | a0001c0001t0018a0001c0001t0038 | 4 | HG02809.hp2 HG03654.hp1 HG06807.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*868_*873delTGTGTG | FAM120C | ENSG00000184083.12 | transcript | ENST00000375180.7 | protein_coding | 16/16 | 868 | chrX | 54072159 | |||||
chrX:54072159
|
TCACACAC others(1): Show |
T | 5 | a0001c0001t0006a0001c0001t0037a0001c0005t0006others(2): Show | 9 | NA18955.hp1 NA18959.hp1 NA18965.hp1 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*866_*873delTGTGTG others(2): Show |
FAM120C | ENSG00000184083.12 | transcript | ENST00000375180.7 | protein_coding | 16/16 | 866 | chrX | 54072159 | |||||
chrX:54072159
|
TCACACAC others(5): Show |
T | 1 | a0001c0001t0036 | 1 | HG01169.hp2 | 3_prime_UTR_variant | MODIFIER | c.*862_*873delTGTGTG others(6): Show |
FAM120C | ENSG00000184083.12 | transcript | ENST00000375180.7 | protein_coding | 16/16 | 862 | chrX | 54072159 | |||||
chrX:54072243
|
T | TC | 1 | a0001c0001t0074 | 1 | HG00609.hp1 | 3_prime_UTR_variant | MODIFIER | c.*789dupG | FAM120C | ENSG00000184083.12 | transcript | ENST00000375180.7 | protein_coding | 16/16 | 789 | chrX | 54072243 | |||||
chrX:54072268
|
T | C | 1 | a0001c0001t0069 | 1 | NA20905.hp1 | 3_prime_UTR_variant | MODIFIER | c.*765A>G | FAM120C | ENSG00000184083.12 | transcript | ENST00000375180.7 | protein_coding | 16/16 | 765 | chrX | 54072268 | |||||
chrX:54072331
|
G | GA | 1 | a0008c0010t0075 | 1 | NA19055.hp1 | 3_prime_UTR_variant | MODIFIER | c.*701dupT | FAM120C | ENSG00000184083.12 | transcript | ENST00000375180.7 | protein_coding | 16/16 | 701 | chrX | 54072331 | |||||
chrX:54072367
|
TC | T | 1 | a0001c0001t0074 | 1 | HG00609.hp1 | 3_prime_UTR_variant | MODIFIER | c.*665delG | FAM120C | ENSG00000184083.12 | transcript | ENST00000375180.7 | protein_coding | 16/16 | 665 | chrX | 54072367 | |||||
chrX:54072392
|
GT | G | 1 | a0001c0001t0070 | 1 | NA19091.hp1 | 3_prime_UTR_variant | MODIFIER | c.*640delA | FAM120C | ENSG00000184083.12 | transcript | ENST00000375180.7 | protein_coding | 16/16 | 640 | chrX | 54072392 | |||||
chrX:54072408
|
T | TA | 1 | a0005c0007t0034 | 1 | NA19075.hp1 | 3_prime_UTR_variant | MODIFIER | c.*624dupT | FAM120C | ENSG00000184083.12 | transcript | ENST00000375180.7 | protein_coding | 16/16 | 624 | chrX | 54072408 | |||||
chrX:54072438
|
AT | A | 1 | a0005c0007t0034 | 1 | NA19075.hp1 | 3_prime_UTR_variant | MODIFIER | c.*594delA | FAM120C | ENSG00000184083.12 | transcript | ENST00000375180.7 | protein_coding | 16/16 | 594 | chrX | 54072438 | |||||
chrX:54072565
|
G | GA | 1 | a0001c0001t0073 | 1 | NA19078.hp1 | 3_prime_UTR_variant | MODIFIER | c.*467dupT | FAM120C | ENSG00000184083.12 | transcript | ENST00000375180.7 | protein_coding | 16/16 | 467 | chrX | 54072565 | |||||
chrX:54072577
|
A | AAC | 3 | a0001c0001t0033a0001c0001t0035a0005c0007t0034 | 4 | HG02559.hp2 HG02647.hp1 NA18972.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*455_*456insGT | FAM120C | ENSG00000184083.12 | transcript | ENST00000375180.7 | protein_coding | 16/16 | 455 | chrX | 54072577 | |||||
chrX:54072578
|
C | A | 3 | a0001c0001t0033a0001c0001t0035a0005c0007t0034 | 4 | HG02559.hp2 HG02647.hp1 NA18972.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*455G>T | FAM120C | ENSG00000184083.12 | transcript | ENST00000375180.7 | protein_coding | 16/16 | 455 | chrX | 54072578 | |||||
chrX:54072578
|
C | CA | 1 | a0001c0009t0071 | 1 | NA18989.hp1 | 3_prime_UTR_variant | MODIFIER | c.*454dupT | FAM120C | ENSG00000184083.12 | transcript | ENST00000375180.7 | protein_coding | 16/16 | 454 | chrX | 54072578 | |||||
chrX:54072578
|
C | CAA | 1 | a0001c0001t0072 | 1 | HG02809.hp1 | 3_prime_UTR_variant | MODIFIER | c.*453_*454dupTT | FAM120C | ENSG00000184083.12 | transcript | ENST00000375180.7 | protein_coding | 16/16 | 454 | chrX | 54072578 | |||||
chrX:54072880
|
A | AG | 1 | a0001c0001t0035 | 1 | NA18972.hp2 | 3_prime_UTR_variant | MODIFIER | c.*152dupC | FAM120C | ENSG00000184083.12 | transcript | ENST00000375180.7 | protein_coding | 16/16 | 152 | chrX | 54072880 | |||||
chrX:54072880
|
AG | A | 1 | a0001c0001t0073 | 1 | NA19078.hp1 | 3_prime_UTR_variant | MODIFIER | c.*152delC | FAM120C | ENSG00000184083.12 | transcript | ENST00000375180.7 | protein_coding | 16/16 | 152 | chrX | 54072880 | |||||
chrX:54072991
|
G | GT | 1 | a0005c0007t0034 | 1 | NA19075.hp1 | 3_prime_UTR_variant | MODIFIER | c.*41dupA | FAM120C | ENSG00000184083.12 | transcript | ENST00000375180.7 | protein_coding | 16/16 | 41 | chrX | 54072991 | |||||
chrX:54072996
|
T | TC | 1 | a0001c0001t0074 | 1 | HG00609.hp1 | 3_prime_UTR_variant | MODIFIER | c.*36dupG | FAM120C | ENSG00000184083.12 | transcript | ENST00000375180.7 | protein_coding | 16/16 | 36 | chrX | 54072996 | |||||
chrX:54183227
|
G | GC | 1 | a0008c0010t0075 | 1 | NA19055.hp1 | 5_prime_UTR_variant | MODIFIER | c.-30dupG | FAM120C | ENSG00000184083.12 | transcript | ENST00000375180.7 | protein_coding | 1/16 | 30 | chrX | 54183227 |
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:54073396
|
AC | A | 1 | a0005c0007t0034g0007 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.3037-110delG | FAM120C | ENSG00000184083.12 | transcript | ENST00000375180.7 | protein_coding | 15/15 | chrX | 54073396 | ||||||
chrX:54073433
|
C | CT | 4 | a0001c0001t0004g0086a0001c0001t0035g0114a0001c0001t0074g0157others(1): Show | 4 | HG00609.hp1 HG01928.hp1 NA18972.hp2 others(1): Show |
intron_variant | MODIFIER | c.3037-147dupA | FAM120C | ENSG00000184083.12 | transcript | ENST00000375180.7 | protein_coding | 15/15 | chrX | 54073433 | ||||||
chrX:54073433
|
CT | C | 4 | a0001c0001t0014g0093a0001c0001t0070g0064a0005c0007t0034g0007others(1): Show | 4 | HG02735.hp1 NA18950.hp2 NA19075.hp1 others(1): Show |
intron_variant | MODIFIER | c.3037-147delA | FAM120C | ENSG00000184083.12 | transcript | ENST00000375180.7 | protein_coding | 15/15 | chrX | 54073433 | ||||||
chrX:54073453
|
CG | C | 1 | a0005c0007t0034g0007 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.3037-167delC | FAM120C | ENSG00000184083.12 | transcript | ENST00000375180.7 | protein_coding | 15/15 | chrX | 54073453 | ||||||
chrX:54073560
|
T | A | 1 | a0001c0001t0072g0106 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.3037-273A>T | FAM120C | ENSG00000184083.12 | transcript | ENST00000375180.7 | protein_coding | 15/15 | chrX | 54073560 | ||||||
chrX:54073620
|
TG | T | 1 | a0005c0007t0034g0007 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.3037-334delC | FAM120C | ENSG00000184083.12 | transcript | ENST00000375180.7 | protein_coding | 15/15 | chrX | 54073620 | ||||||
chrX:54073661
|
G | GC | 1 | a0005c0007t0034g0007 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.3037-375dupG | FAM120C | ENSG00000184083.12 | transcript | ENST00000375180.7 | protein_coding | 15/15 | chrX | 54073661 | ||||||
chrX:54073779
|
C | CA | 1 | a0005c0007t0034g0007 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.3037-493dupT | FAM120C | ENSG00000184083.12 | transcript | ENST00000375180.7 | protein_coding | 15/15 | chrX | 54073779 | ||||||
chrX:54073802
|
A | T | 1 | a0005c0007t0034g0007 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.3037-515T>A | FAM120C | ENSG00000184083.12 | transcript | ENST00000375180.7 | protein_coding | 15/15 | chrX | 54073802 | ||||||
chrX:54073831
|
C | CT | 1 | a0001c0001t0074g0157 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.3037-545dupA | FAM120C | ENSG00000184083.12 | transcript | ENST00000375180.7 | protein_coding | 15/15 | chrX | 54073831 | ||||||
chrX:54073944
|
GC | G | 1 | a0008c0010t0075g0188 | 1 | NA19055.hp1 | intron_variant | MODIFIER | c.3037-658delG | FAM120C | ENSG00000184083.12 | transcript | ENST00000375180.7 | protein_coding | 15/15 | chrX | 54073944 | ||||||
chrX:54073958
|
TG | T | 1 | a0005c0007t0034g0007 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.3037-672delC | FAM120C | ENSG00000184083.12 | transcript | ENST00000375180.7 | protein_coding | 15/15 | chrX | 54073958 | ||||||
chrX:54074204
|
C | T | 4 | a0001c0001t0005g0062a0001c0001t0010g0065a0001c0001t0024g0067others(1): Show | 4 | NA18948.hp1 NA18971.hp1 NA19058.hp1 others(1): Show |
intron_variant | MODIFIER | c.3037-917G>A | FAM120C | ENSG00000184083.12 | transcript | ENST00000375180.7 | protein_coding | 15/15 | chrX | 54074204 | ||||||
chrX:54074357
|
G | A | 46 | a0001c0001t0002g0132a0001c0001t0002g0153a0001c0001t0002g0159others(43): Show | 47 | HG00558.hp2 HG00609.hp1 HG00621.hp1 others(44): Show |
intron_variant | MODIFIER | c.3037-1070C>T | FAM120C | ENSG00000184083.12 | transcript | ENST00000375180.7 | protein_coding | 15/15 | chrX | 54074357 | ||||||
chrX:54074374
|
G | GA | 2 | a0001c0001t0002g0168a0001c0001t0010g0072 | 2 | NA18950.hp1 NA18969.hp1 |
intron_variant | MODIFIER | c.3037-1088dupT | FAM120C | ENSG00000184083.12 | transcript | ENST00000375180.7 | protein_coding | 15/15 | chrX | 54074374 | ||||||
chrX:54074606
|
G | A | 8 | a0001c0001t0001g0060a0001c0001t0001g0061a0001c0001t0005g0037others(5): Show | 8 | HG00558.hp1 NA18969.hp1 NA18983.hp1 others(5): Show |
intron_variant | MODIFIER | c.3037-1319C>T | FAM120C | ENSG00000184083.12 | transcript | ENST00000375180.7 | protein_coding | 15/15 | chrX | 54074606 | ||||||
chrX:54074609
|
A | AT | 1 | a0001c0001t0074g0157 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.3037-1323dupA | FAM120C | ENSG00000184083.12 | transcript | ENST00000375180.7 | protein_coding | 15/15 | chrX | 54074609 | ||||||
chrX:54074637
|
G | C | 1 | a0001c0001t0029g0068 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.3037-1350C>G | FAM120C | ENSG00000184083.12 | transcript | ENST00000375180.7 | protein_coding | 15/15 | chrX | 54074637 | ||||||
chrX:54074715
|
A | G | 1 | a0001c0001t0017g0176 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.3037-1428T>C | FAM120C | ENSG00000184083.12 | transcript | ENST00000375180.7 | protein_coding | 15/15 | chrX | 54074715 | ||||||
chrX:54074916
|
A | G | 1 | a0002c0002t0047g0185 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.3037-1629T>C | FAM120C | ENSG00000184083.12 | transcript | ENST00000375180.7 | protein_coding | 15/15 | chrX | 54074916 | ||||||
chrX:54075207
|
G | A | 1 | a0001c0001t0067g0018 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.3037-1920C>T | FAM120C | ENSG00000184083.12 | transcript | ENST00000375180.7 | protein_coding | 15/15 | chrX | 54075207 | ||||||
chrX:54075270
|
A | AG | 1 | a0001c0001t0074g0157 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.3037-1984dupC | FAM120C | ENSG00000184083.12 | transcript | ENST00000375180.7 | protein_coding | 15/15 | chrX | 54075270 | ||||||
chrX:54075465
|
C | A | 187 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0022others(184): Show | 189 | HG00140.hp1 HG00280.hp1 HG00558.hp1 others(186): Show |
intron_variant | MODIFIER | c.3037-2178G>T | FAM120C | ENSG00000184083.12 | transcript | ENST00000375180.7 | protein_coding | 15/15 | chrX | 54075465 | ||||||
chrX:54075797
|
C | CA | 3 | a0001c0001t0005g0095a0001c0001t0056g0103a0002c0002t0007g0184 | 3 | HG01192.hp1 HG03209.hp1 NA18985.hp1 |
intron_variant | MODIFIER | c.3037-2511dupT | FAM120C | ENSG00000184083.12 | transcript | ENST00000375180.7 | protein_coding | 15/15 | chrX | 54075797 | ||||||
chrX:54075797
|
CA | C | 2 | a0001c0001t0009g0049a0001c0001t0024g0067 | 2 | NA18948.hp1 NA19083.hp1 |
intron_variant | MODIFIER | c.3037-2511delT | FAM120C | ENSG00000184083.12 | transcript | ENST00000375180.7 | protein_coding | 15/15 | chrX | 54075797 | ||||||
chrX:54075814
|
A | G | 5 | a0001c0001t0018g0115a0001c0001t0018g0116a0001c0001t0018g0151others(2): Show | 5 | HG02615.hp2 HG02809.hp2 HG06807.hp1 others(2): Show |
intron_variant | MODIFIER | c.3037-2527T>C | FAM120C | ENSG00000184083.12 | transcript | ENST00000375180.7 | protein_coding | 15/15 | chrX | 54075814 | ||||||
chrX:54075872
|
C | T | 187 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0022others(184): Show | 189 | HG00140.hp1 HG00280.hp1 HG00558.hp1 others(186): Show |
intron_variant | MODIFIER | c.3037-2585G>A | FAM120C | ENSG00000184083.12 | transcript | ENST00000375180.7 | protein_coding | 15/15 | chrX | 54075872 | ||||||
chrX:54075875
|
G | A | 1 | a0001c0001t0024g0080 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.3037-2588C>T | FAM120C | ENSG00000184083.12 | transcript | ENST00000375180.7 | protein_coding | 15/15 | chrX | 54075875 | ||||||
chrX:54075900
|
G | T | 1 | a0001c0001t0006g0029 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.3037-2613C>A | FAM120C | ENSG00000184083.12 | transcript | ENST00000375180.7 | protein_coding | 15/15 | chrX | 54075900 | ||||||
chrX:54075970
|
G | A | 2 | a0001c0001t0050g0051a0001c0001t0055g0048 | 2 | HG02071.hp1 NA18952.hp1 |
intron_variant | MODIFIER | c.3037-2683C>T | FAM120C | ENSG00000184083.12 | transcript | ENST00000375180.7 | protein_coding | 15/15 | chrX | 54075970 | ||||||
chrX:54075988
|
C | T | 1 | a0002c0002t0019g0186 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.3037-2701G>A | FAM120C | ENSG00000184083.12 | transcript | ENST00000375180.7 | protein_coding | 15/15 | chrX | 54075988 | ||||||
chrX:54076117
|
T | A | 1 | a0001c0001t0029g0068 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.3037-2830A>T | FAM120C | ENSG00000184083.12 | transcript | ENST00000375180.7 | protein_coding | 15/15 | chrX | 54076117 | ||||||
chrX:54076153
|
A | G | 5 | a0001c0001t0018g0115a0001c0001t0018g0116a0001c0001t0018g0151others(2): Show | 5 | HG02615.hp2 HG02809.hp2 HG06807.hp1 others(2): Show |
intron_variant | MODIFIER | c.3037-2866T>C | FAM120C | ENSG00000184083.12 | transcript | ENST00000375180.7 | protein_coding | 15/15 | chrX | 54076153 | ||||||
chrX:54076327
|
T | C | 1 | a0001c0001t0003g0181 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.3037-3040A>G | FAM120C | ENSG00000184083.12 | transcript | ENST00000375180.7 | protein_coding | 15/15 | chrX | 54076327 | ||||||
chrX:54076329
|
TA | T | 2 | a0001c0001t0043g0147a0001c0001t0066g0076 | 2 | HG02922.hp2 NA19089.hp1 |
intron_variant | MODIFIER | c.3037-3043delT | FAM120C | ENSG00000184083.12 | transcript | ENST00000375180.7 | protein_coding | 15/15 | chrX | 54076329 | ||||||
chrX:54076330
|
A | T | 1 | a0001c0001t0019g0120 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.3037-3043T>A | FAM120C | ENSG00000184083.12 | transcript | ENST00000375180.7 | protein_coding | 15/15 | chrX | 54076330 | ||||||
chrX:54076345
|
C | CA | 7 | a0001c0001t0007g0017a0001c0001t0007g0054a0001c0001t0007g0055others(4): Show | 7 | NA18747.hp1 NA18953.hp1 NA18957.hp2 others(4): Show |
intron_variant | MODIFIER | c.3037-3059dupT | FAM120C | ENSG00000184083.12 | transcript | ENST00000375180.7 | protein_coding | 15/15 | chrX | 54076345 | ||||||
chrX:54076345
|
C | CAA | 1 | a0001c0001t0007g0057 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.3037-3060_3037-305 others(6): Show |
FAM120C | ENSG00000184083.12 | transcript | ENST00000375180.7 | protein_coding | 15/15 | chrX | 54076345 | ||||||
chrX:54076345
|
CA | C | 2 | a0001c0001t0043g0147a0001c0001t0045g0148 | 2 | HG02922.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.3037-3059delT | FAM120C | ENSG00000184083.12 | transcript | ENST00000375180.7 | protein_coding | 15/15 | chrX | 54076345 | ||||||
chrX:54076491
|
C | T | 1 | a0001c0001t0001g0022 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.3037-3204G>A | FAM120C | ENSG00000184083.12 | transcript | ENST00000375180.7 | protein_coding | 15/15 | chrX | 54076491 | ||||||
chrX:54076952
|
C | T | 23 | a0001c0001t0013g0112a0001c0001t0015g0015a0001c0001t0015g0097others(20): Show | 23 | HG00735.hp2 HG00738.hp1 HG01243.hp1 others(20): Show |
intron_variant | MODIFIER | c.3036+3280G>A | FAM120C | ENSG00000184083.12 | transcript | ENST00000375180.7 | protein_coding | 15/15 | chrX | 54076952 | ||||||
chrX:54077102
|
T | C | 1 | a0001c0001t0031g0145 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.3036+3130A>G | FAM120C | ENSG00000184083.12 | transcript | ENST00000375180.7 | protein_coding | 15/15 | chrX | 54077102 | ||||||
chrX:54077207
|
A | G | 187 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0022others(184): Show | 189 | HG00140.hp1 HG00280.hp1 HG00558.hp1 others(186): Show |
intron_variant | MODIFIER | c.3036+3025T>C | FAM120C | ENSG00000184083.12 | transcript | ENST00000375180.7 | protein_coding | 15/15 | chrX | 54077207 | ||||||
chrX:54077676
|
T | A | 1 | a0001c0001t0017g0154 | 1 | HG01257.hp2 | intron_variant | MODIFIER | c.3036+2556A>T | FAM120C | ENSG00000184083.12 | transcript | ENST00000375180.7 | protein_coding | 15/15 | chrX | 54077676 | ||||||
chrX:54077908
|
G | C | 187 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0022others(184): Show | 189 | HG00140.hp1 HG00280.hp1 HG00558.hp1 others(186): Show |
intron_variant | MODIFIER | c.3036+2324C>G | FAM120C | ENSG00000184083.12 | transcript | ENST00000375180.7 | protein_coding | 15/15 | chrX | 54077908 | ||||||
chrX:54077939
|
C | CT | 42 | a0001c0001t0002g0132a0001c0001t0002g0153a0001c0001t0002g0159others(39): Show | 43 | HG00558.hp2 HG00609.hp1 HG01070.hp1 others(40): Show |
intron_variant | MODIFIER | c.3036+2292dupA | FAM120C | ENSG00000184083.12 | transcript | ENST00000375180.7 | protein_coding | 15/15 | chrX | 54077939 | ||||||
chrX:54077939
|
C | CTT | 97 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0022others(94): Show | 98 | HG00140.hp1 HG00280.hp1 HG00558.hp1 others(95): Show |
intron_variant | MODIFIER | c.3036+2291_3036+229 others(6): Show |
FAM120C | ENSG00000184083.12 | transcript | ENST00000375180.7 | protein_coding | 15/15 | chrX | 54077939 | ||||||
chrX:54077939
|
C | CTTT | 9 | a0001c0001t0001g0036a0001c0001t0001g0060a0001c0001t0003g0038others(6): Show | 9 | HG01358.hp1 HG04199.hp1 NA18940.hp1 others(6): Show |
intron_variant | MODIFIER | c.3036+2290_3036+229 others(7): Show |
FAM120C | ENSG00000184083.12 | transcript | ENST00000375180.7 | protein_coding | 15/15 | chrX | 54077939 | ||||||
chrX:54078095
|
T | C | 3 | a0001c0001t0022g0119a0001c0001t0043g0147a0001c0001t0045g0148 | 3 | HG02922.hp2 HG03471.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.3036+2137A>G | FAM120C | ENSG00000184083.12 | transcript | ENST00000375180.7 | protein_coding | 15/15 | chrX | 54078095 | ||||||
chrX:54078132
|
A | G | 1 | a0001c0001t0022g0119 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.3036+2100T>C | FAM120C | ENSG00000184083.12 | transcript | ENST00000375180.7 | protein_coding | 15/15 | chrX | 54078132 | ||||||
chrX:54078178
|
C | T | 1 | a0001c0001t0038g0090 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.3036+2054G>A | FAM120C | ENSG00000184083.12 | transcript | ENST00000375180.7 | protein_coding | 15/15 | chrX | 54078178 | ||||||
chrX:54078537
|
C | G | 187 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0022others(184): Show | 189 | HG00140.hp1 HG00280.hp1 HG00558.hp1 others(186): Show |
intron_variant | MODIFIER | c.3036+1695G>C | FAM120C | ENSG00000184083.12 | transcript | ENST00000375180.7 | protein_coding | 15/15 | chrX | 54078537 | ||||||
chrX:54078996
|
C | CA | 2 | a0001c0001t0020g0131a0001c0001t0050g0051 | 2 | NA18952.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.3036+1235dupT | FAM120C | ENSG00000184083.12 | transcript | ENST00000375180.7 | protein_coding | 15/15 | chrX | 54078996 | ||||||
chrX:54079217
|
G | A | 2 | a0001c0001t0043g0147a0001c0001t0045g0148 | 2 | HG02922.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.3036+1015C>T | FAM120C | ENSG00000184083.12 | transcript | ENST00000375180.7 | protein_coding | 15/15 | chrX | 54079217 | ||||||
chrX:54079248
|
C | T | 1 | a0001c0001t0025g0135 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.3036+984G>A | FAM120C | ENSG00000184083.12 | transcript | ENST00000375180.7 | protein_coding | 15/15 | chrX | 54079248 | ||||||
chrX:54079260
|
C | CA | 8 | a0001c0001t0001g0061a0001c0001t0009g0073a0001c0001t0010g0072others(5): Show | 8 | HG02135.hp1 HG02257.hp1 HG02809.hp1 others(5): Show |
intron_variant | MODIFIER | c.3036+971dupT | FAM120C | ENSG00000184083.12 | transcript | ENST00000375180.7 | protein_coding | 15/15 | chrX | 54079260 | ||||||
chrX:54079260
|
CA | C | 2 | a0001c0001t0003g0032a0001c0001t0025g0135 | 2 | HG02895.hp1 NA18986.hp1 |
intron_variant | MODIFIER | c.3036+971delT | FAM120C | ENSG00000184083.12 | transcript | ENST00000375180.7 | protein_coding | 15/15 | chrX | 54079260 | ||||||
chrX:54079441
|
C | CGA | 4 | a0001c0001t0005g0095a0001c0001t0033g0012a0001c0001t0033g0013others(1): Show | 4 | HG02559.hp2 HG02647.hp1 HG02809.hp1 others(1): Show |
intron_variant | MODIFIER | c.3036+789_3036+790d others(4): Show |
FAM120C | ENSG00000184083.12 | transcript | ENST00000375180.7 | protein_coding | 15/15 | chrX | 54079441 | ||||||
chrX:54079441
|
C | CGAGAGA | 1 | a0001c0001t0055g0048 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.3036+785_3036+790d others(8): Show |
FAM120C | ENSG00000184083.12 | transcript | ENST00000375180.7 | protein_coding | 15/15 | chrX | 54079441 | ||||||
chrX:54079527
|
G | A | 1 | a0001c0001t0004g0021 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.3036+705C>T | FAM120C | ENSG00000184083.12 | transcript | ENST00000375180.7 | protein_coding | 15/15 | chrX | 54079527 | ||||||
chrX:54079797
|
C | CA | 3 | a0001c0001t0033g0012a0001c0001t0033g0013a0001c0001t0072g0106 | 3 | HG02559.hp2 HG02647.hp1 HG02809.hp1 |
intron_variant | MODIFIER | c.3036+434dupT | FAM120C | ENSG00000184083.12 | transcript | ENST00000375180.7 | protein_coding | 15/15 | chrX | 54079797 | ||||||
chrX:54080185
|
C | T | 10 | a0001c0001t0016g0137a0001c0001t0016g0139a0001c0001t0016g0141others(7): Show | 10 | HG01255.hp1 HG01884.hp2 HG02055.hp1 others(7): Show |
intron_variant | MODIFIER | c.3036+47G>A | FAM120C | ENSG00000184083.12 | transcript | ENST00000375180.7 | protein_coding | 15/15 | chrX | 54080185 | ||||||
chrX:54080505
|
T | C | 1 | a0001c0001t0021g0077 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.2979-216A>G | FAM120C | ENSG00000184083.12 | transcript | ENST00000375180.7 | protein_coding | 14/15 | chrX | 54080505 | ||||||
chrX:54080626
|
G | A | 2 | a0001c0001t0015g0015a0001c0001t0022g0016 | 2 | HG01884.hp1 HG02717.hp1 |
intron_variant | MODIFIER | c.2979-337C>T | FAM120C | ENSG00000184083.12 | transcript | ENST00000375180.7 | protein_coding | 14/15 | chrX | 54080626 | ||||||
chrX:54080799
|
T | A | 1 | a0001c0001t0033g0013 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.2979-510A>T | FAM120C | ENSG00000184083.12 | transcript | ENST00000375180.7 | protein_coding | 14/15 | chrX | 54080799 | ||||||
chrX:54080818
|
C | T | 1 | a0001c0001t0056g0103 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.2978+504G>A | FAM120C | ENSG00000184083.12 | transcript | ENST00000375180.7 | protein_coding | 14/15 | chrX | 54080818 | ||||||
chrX:54080860
|
C | T | 9 | a0001c0001t0006g0026a0001c0001t0006g0028a0001c0001t0006g0029others(6): Show | 9 | NA18955.hp1 NA18959.hp1 NA18965.hp1 others(6): Show |
intron_variant | MODIFIER | c.2978+462G>A | FAM120C | ENSG00000184083.12 | transcript | ENST00000375180.7 | protein_coding | 14/15 | chrX | 54080860 | ||||||
chrX:54080863
|
G | GA | 129 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0022others(126): Show | 130 | HG00140.hp1 HG00280.hp1 HG00558.hp1 others(127): Show |
intron_variant | MODIFIER | c.2978+458dupT | FAM120C | ENSG00000184083.12 | transcript | ENST00000375180.7 | protein_coding | 14/15 | chrX | 54080863 | ||||||
chrX:54080863
|
G | GAA | 1 | a0001c0001t0010g0072 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.2978+457_2978+458d others(4): Show |
FAM120C | ENSG00000184083.12 | transcript | ENST00000375180.7 | protein_coding | 14/15 | chrX | 54080863 | ||||||
chrX:54080863
|
GA | G | 1 | a0001c0001t0018g0115 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.2978+458delT | FAM120C | ENSG00000184083.12 | transcript | ENST00000375180.7 | protein_coding | 14/15 | chrX | 54080863 | ||||||
chrX:54081259
|
T | C | 187 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0022others(184): Show | 189 | HG00140.hp1 HG00280.hp1 HG00558.hp1 others(186): Show |
intron_variant | MODIFIER | c.2978+63A>G | FAM120C | ENSG00000184083.12 | transcript | ENST00000375180.7 | protein_coding | 14/15 | chrX | 54081259 | ||||||
chrX:54081274
|
G | T | 3 | a0001c0001t0033g0012a0001c0001t0033g0013a0001c0001t0072g0106 | 3 | HG02559.hp2 HG02647.hp1 HG02809.hp1 |
intron_variant | MODIFIER | c.2978+48C>A | FAM120C | ENSG00000184083.12 | transcript | ENST00000375180.7 | protein_coding | 14/15 | chrX | 54081274 | ||||||
chrX:54081774
|
G | GA | 2 | a0001c0001t0026g0101a0001c0001t0074g0157 | 2 | HG00609.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.2840-315dupT | FAM120C | ENSG00000184083.12 | transcript | ENST00000375180.7 | protein_coding | 13/15 | chrX | 54081774 | ||||||
chrX:54081774
|
GA | G | 1 | a0001c0001t0017g0171 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.2840-315delT | FAM120C | ENSG00000184083.12 | transcript | ENST00000375180.7 | protein_coding | 13/15 | chrX | 54081774 | ||||||
chrX:54081869
|
T | C | 187 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0022others(184): Show | 189 | HG00140.hp1 HG00280.hp1 HG00558.hp1 others(186): Show |
intron_variant | MODIFIER | c.2840-409A>G | FAM120C | ENSG00000184083.12 | transcript | ENST00000375180.7 | protein_coding | 13/15 | chrX | 54081869 | ||||||
chrX:54082000
|
T | G | 2 | a0001c0001t0012g0035a0001c0001t0012g0047 | 2 | HG03942.hp1 HG04228.hp1 |
intron_variant | MODIFIER | c.2840-540A>C | FAM120C | ENSG00000184083.12 | transcript | ENST00000375180.7 | protein_coding | 13/15 | chrX | 54082000 | ||||||
chrX:54082054
|
G | A | 2 | a0001c0001t0010g0023a0001c0001t0010g0072 | 2 | NA18969.hp1 NA19062.hp1 |
intron_variant | MODIFIER | c.2840-594C>T | FAM120C | ENSG00000184083.12 | transcript | ENST00000375180.7 | protein_coding | 13/15 | chrX | 54082054 | ||||||
chrX:54082187
|
C | CA | 5 | a0001c0001t0007g0057a0001c0001t0010g0092a0001c0001t0019g0120others(2): Show | 5 | HG02257.hp1 HG03486.hp2 HG03492.hp1 others(2): Show |
intron_variant | MODIFIER | c.2840-728dupT | FAM120C | ENSG00000184083.12 | transcript | ENST00000375180.7 | protein_coding | 13/15 | chrX | 54082187 | ||||||
chrX:54082187
|
CA | C | 5 | a0001c0001t0001g0061a0001c0001t0005g0062a0001c0001t0009g0073others(2): Show | 5 | HG02895.hp1 NA18612.hp1 NA19009.hp1 others(2): Show |
intron_variant | MODIFIER | c.2840-728delT | FAM120C | ENSG00000184083.12 | transcript | ENST00000375180.7 | protein_coding | 13/15 | chrX | 54082187 | ||||||
chrX:54082261
|
G | A | 3 | a0001c0001t0033g0012a0001c0001t0033g0013a0001c0001t0072g0106 | 3 | HG02559.hp2 HG02647.hp1 HG02809.hp1 |
intron_variant | MODIFIER | c.2840-801C>T | FAM120C | ENSG00000184083.12 | transcript | ENST00000375180.7 | protein_coding | 13/15 | chrX | 54082261 | ||||||
chrX:54082565
|
T | C | 187 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0022others(184): Show | 189 | HG00140.hp1 HG00280.hp1 HG00558.hp1 others(186): Show |
intron_variant | MODIFIER | c.2840-1105A>G | FAM120C | ENSG00000184083.12 | transcript | ENST00000375180.7 | protein_coding | 13/15 | chrX | 54082565 | ||||||
chrX:54082943
|
C | T | 1 | a0001c0001t0015g0097 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.2840-1483G>A | FAM120C | ENSG00000184083.12 | transcript | ENST00000375180.7 | protein_coding | 13/15 | chrX | 54082943 | ||||||
chrX:54082979
|
C | T | 3 | a0001c0001t0013g0112a0001c0001t0019g0111a0001c0001t0052g0100 | 3 | HG00738.hp1 HG02630.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.2840-1519G>A | FAM120C | ENSG00000184083.12 | transcript | ENST00000375180.7 | protein_coding | 13/15 | chrX | 54082979 | ||||||
chrX:54083123
|
GA | G | 1 | a0001c0001t0004g0006 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.2840-1664delT | FAM120C | ENSG00000184083.12 | transcript | ENST00000375180.7 | protein_coding | 13/15 | chrX | 54083123 | ||||||
chrX:54083433
|
C | CACACA | 1 | a0001c0001t0008g0170 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.2840-1974_2840-197 others(9): Show |
FAM120C | ENSG00000184083.12 | transcript | ENST00000375180.7 | protein_coding | 13/15 | chrX | 54083433 | ||||||
chrX:54083433
|
C | CCA | 8 | a0001c0001t0003g0084a0001c0001t0006g0026a0001c0001t0009g0034others(5): Show | 9 | HG01934.hp1 HG02056.hp1 HG02257.hp2 others(6): Show |
intron_variant | MODIFIER | c.2840-1975_2840-197 others(6): Show |
FAM120C | ENSG00000184083.12 | transcript | ENST00000375180.7 | protein_coding | 13/15 | chrX | 54083433 | ||||||
chrX:54083433
|
C | CCACA | 61 | a0001c0001t0001g0008a0001c0001t0001g0022a0001c0001t0001g0025others(58): Show | 61 | HG00140.hp1 HG00280.hp1 HG00558.hp1 others(58): Show |
intron_variant | MODIFIER | c.2840-1977_2840-197 others(8): Show |
FAM120C | ENSG00000184083.12 | transcript | ENST00000375180.7 | protein_coding | 13/15 | chrX | 54083433 | ||||||
chrX:54083433
|
C | CCACACA | 45 | a0001c0001t0001g0042a0001c0001t0001g0044a0001c0001t0001g0060others(42): Show | 45 | HG00558.hp2 HG00642.hp1 HG01081.hp2 others(42): Show |
intron_variant | MODIFIER | c.2840-1979_2840-197 others(10): Show |
FAM120C | ENSG00000184083.12 | transcript | ENST00000375180.7 | protein_coding | 13/15 | chrX | 54083433 | ||||||
chrX:54083433
|
C | CCACACAC others(1): Show |
19 | a0001c0001t0001g0001a0001c0001t0001g0036a0001c0001t0002g0172others(16): Show | 20 | HG01070.hp1 HG01070.hp2 HG01074.hp1 others(17): Show |
intron_variant | MODIFIER | c.2840-1981_2840-197 others(12): Show |
FAM120C | ENSG00000184083.12 | transcript | ENST00000375180.7 | protein_coding | 13/15 | chrX | 54083433 | ||||||
chrX:54083433
|
C | CCACACAC others(3): Show |
5 | a0001c0001t0002g0132a0001c0001t0021g0014a0001c0001t0023g0109others(2): Show | 5 | HG01081.hp1 HG01884.hp2 HG02027.hp1 others(2): Show |
intron_variant | MODIFIER | c.2840-1983_2840-197 others(14): Show |
FAM120C | ENSG00000184083.12 | transcript | ENST00000375180.7 | protein_coding | 13/15 | chrX | 54083433 | ||||||
chrX:54083433
|
C | CCACACAC others(5): Show |
7 | a0001c0001t0008g0124a0001c0001t0012g0047a0001c0001t0016g0137others(4): Show | 7 | HG02451.hp2 HG02486.hp1 HG02559.hp1 others(4): Show |
intron_variant | MODIFIER | c.2840-1985_2840-197 others(16): Show |
FAM120C | ENSG00000184083.12 | transcript | ENST00000375180.7 | protein_coding | 13/15 | chrX | 54083433 | ||||||
chrX:54083433
|
C | CCACACAC others(7): Show |
3 | a0001c0001t0016g0141a0001c0001t0016g0142a0001c0001t0043g0147 | 3 | HG02055.hp1 HG02922.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.2840-1987_2840-197 others(18): Show |
FAM120C | ENSG00000184083.12 | transcript | ENST00000375180.7 | protein_coding | 13/15 | chrX | 54083433 | ||||||
chrX:54083433
|
C | CCACACAC others(9): Show |
1 | a0001c0001t0067g0018 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.2840-1989_2840-197 others(20): Show |
FAM120C | ENSG00000184083.12 | transcript | ENST00000375180.7 | protein_coding | 13/15 | chrX | 54083433 | ||||||
chrX:54083433
|
C | CCACACAC others(11): Show |
1 | a0001c0001t0031g0145 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.2840-1991_2840-197 others(22): Show |
FAM120C | ENSG00000184083.12 | transcript | ENST00000375180.7 | protein_coding | 13/15 | chrX | 54083433 | ||||||
chrX:54083433
|
C | CCACACAC others(15): Show |
1 | a0001c0001t0013g0130 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.2840-1995_2840-197 others(26): Show |
FAM120C | ENSG00000184083.12 | transcript | ENST00000375180.7 | protein_coding | 13/15 | chrX | 54083433 | ||||||
chrX:54083433
|
CCA | C | 6 | a0001c0001t0019g0120a0001c0001t0022g0119a0001c0001t0025g0135others(3): Show | 6 | HG02895.hp1 HG03098.hp1 HG03486.hp2 others(3): Show |
intron_variant | MODIFIER | c.2840-1975_2840-197 others(6): Show |
FAM120C | ENSG00000184083.12 | transcript | ENST00000375180.7 | protein_coding | 13/15 | chrX | 54083433 | ||||||
chrX:54083433
|
CCACA | C | 13 | a0001c0001t0015g0015a0001c0001t0015g0097a0001c0001t0015g0133others(10): Show | 13 | HG00735.hp1 HG00735.hp2 HG01243.hp1 others(10): Show |
intron_variant | MODIFIER | c.2840-1977_2840-197 others(8): Show |
FAM120C | ENSG00000184083.12 | transcript | ENST00000375180.7 | protein_coding | 13/15 | chrX | 54083433 | ||||||
chrX:54083433
|
CCACACA | C | 8 | a0001c0001t0013g0112a0001c0001t0018g0115a0001c0001t0018g0116others(5): Show | 8 | HG02145.hp1 HG02615.hp2 HG02630.hp1 others(5): Show |
intron_variant | MODIFIER | c.2840-1979_2840-197 others(10): Show |
FAM120C | ENSG00000184083.12 | transcript | ENST00000375180.7 | protein_coding | 13/15 | chrX | 54083433 | ||||||
chrX:54083433
|
CCACACAC others(1): Show |
C | 1 | a0001c0001t0052g0100 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.2840-1981_2840-197 others(12): Show |
FAM120C | ENSG00000184083.12 | transcript | ENST00000375180.7 | protein_coding | 13/15 | chrX | 54083433 | ||||||
chrX:54083433
|
CCACACAC others(5): Show |
C | 1 | a0001c0001t0065g0083 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.2840-1985_2840-197 others(16): Show |
FAM120C | ENSG00000184083.12 | transcript | ENST00000375180.7 | protein_coding | 13/15 | chrX | 54083433 | ||||||
chrX:54083477
|
A | C | 2 | a0001c0001t0008g0170a0001c0001t0022g0149 | 2 | HG03516.hp1 NA19082.hp1 |
intron_variant | MODIFIER | c.2840-2017T>G | FAM120C | ENSG00000184083.12 | transcript | ENST00000375180.7 | protein_coding | 13/15 | chrX | 54083477 | ||||||
chrX:54083478
|
C | CACACA | 1 | a0004c0008t0009g0105 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.2840-2019_2840-201 others(9): Show |
FAM120C | ENSG00000184083.12 | transcript | ENST00000375180.7 | protein_coding | 13/15 | chrX | 54083478 | ||||||
chrX:54083478
|
C | CACACACA others(6): Show |
1 | a0001c0001t0003g0181 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.2840-2019_2840-201 others(17): Show |
FAM120C | ENSG00000184083.12 | transcript | ENST00000375180.7 | protein_coding | 13/15 | chrX | 54083478 | ||||||
chrX:54083705
|
G | C | 1 | a0001c0001t0022g0149 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.2839+2010C>G | FAM120C | ENSG00000184083.12 | transcript | ENST00000375180.7 | protein_coding | 13/15 | chrX | 54083705 | ||||||
chrX:54083869
|
G | A | 2 | a0001c0001t0002g0132a0001c0001t0020g0131 | 2 | HG01081.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.2839+1846C>T | FAM120C | ENSG00000184083.12 | transcript | ENST00000375180.7 | protein_coding | 13/15 | chrX | 54083869 | ||||||
chrX:54084144
|
G | A | 1 | a0001c0001t0009g0073 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.2839+1571C>T | FAM120C | ENSG00000184083.12 | transcript | ENST00000375180.7 | protein_coding | 13/15 | chrX | 54084144 | ||||||
chrX:54084516
|
G | A | 8 | a0001c0001t0018g0115a0001c0001t0018g0116a0001c0001t0018g0151others(5): Show | 8 | HG02559.hp2 HG02615.hp2 HG02647.hp1 others(5): Show |
intron_variant | MODIFIER | c.2839+1199C>T | FAM120C | ENSG00000184083.12 | transcript | ENST00000375180.7 | protein_coding | 13/15 | chrX | 54084516 | ||||||
chrX:54084714
|
C | CA | 1 | a0001c0001t0039g0150 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.2839+1000dupT | FAM120C | ENSG00000184083.12 | transcript | ENST00000375180.7 | protein_coding | 13/15 | chrX | 54084714 | ||||||
chrX:54084714
|
CA | C | 2 | a0001c0001t0012g0043a0001c0001t0072g0106 | 2 | HG02809.hp1 HG03490.hp1 |
intron_variant | MODIFIER | c.2839+1000delT | FAM120C | ENSG00000184083.12 | transcript | ENST00000375180.7 | protein_coding | 13/15 | chrX | 54084714 | ||||||
chrX:54084714
|
CAA | C | 169 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0022others(166): Show | 171 | HG00140.hp1 HG00280.hp1 HG00558.hp1 others(168): Show |
intron_variant | MODIFIER | c.2839+999_2839+1000 others(5): Show |
FAM120C | ENSG00000184083.12 | transcript | ENST00000375180.7 | protein_coding | 13/15 | chrX | 54084714 | ||||||
chrX:54084714
|
CAAA | C | 8 | a0001c0001t0003g0087a0001c0001t0003g0110a0001c0001t0004g0006others(5): Show | 8 | HG01070.hp2 HG01433.hp1 HG02300.hp1 others(5): Show |
intron_variant | MODIFIER | c.2839+998_2839+1000 others(6): Show |
FAM120C | ENSG00000184083.12 | transcript | ENST00000375180.7 | protein_coding | 13/15 | chrX | 54084714 | ||||||
chrX:54084868
|
G | A | 1 | a0001c0001t0001g0177 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.2839+847C>T | FAM120C | ENSG00000184083.12 | transcript | ENST00000375180.7 | protein_coding | 13/15 | chrX | 54084868 | ||||||
chrX:54085501
|
C | T | 2 | a0001c0001t0012g0035a0001c0001t0012g0047 | 2 | HG03942.hp1 HG04228.hp1 |
intron_variant | MODIFIER | c.2839+214G>A | FAM120C | ENSG00000184083.12 | transcript | ENST00000375180.7 | protein_coding | 13/15 | chrX | 54085501 | ||||||
chrX:54085579
|
C | T | 1 | a0001c0001t0067g0018 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.2839+136G>A | FAM120C | ENSG00000184083.12 | transcript | ENST00000375180.7 | protein_coding | 13/15 | chrX | 54085579 | ||||||
chrX:54085586
|
TA | T | 2 | a0001c0001t0010g0091a0001c0001t0025g0135 | 2 | HG02895.hp1 NA18612.hp1 |
intron_variant | MODIFIER | c.2839+128delT | FAM120C | ENSG00000184083.12 | transcript | ENST00000375180.7 | protein_coding | 13/15 | chrX | 54085586 | ||||||
chrX:54086066
|
C | T | 1 | a0001c0001t0019g0120 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.2638-150G>A | FAM120C | ENSG00000184083.12 | transcript | ENST00000375180.7 | protein_coding | 12/15 | chrX | 54086066 | ||||||
chrX:54086516
|
G | A | 1 | a0001c0001t0056g0103 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.2638-600C>T | FAM120C | ENSG00000184083.12 | transcript | ENST00000375180.7 | protein_coding | 12/15 | chrX | 54086516 | ||||||
chrX:54086597
|
T | C | 1 | a0001c0001t0003g0084 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.2638-681A>G | FAM120C | ENSG00000184083.12 | transcript | ENST00000375180.7 | protein_coding | 12/15 | chrX | 54086597 | ||||||
chrX:54086647
|
TGGGA | T | 11 | a0001c0001t0015g0097a0001c0001t0015g0133a0001c0001t0015g0136others(8): Show | 11 | HG02630.hp2 HG02895.hp1 HG02896.hp1 others(8): Show |
intron_variant | MODIFIER | c.2638-735_2638-732d others(6): Show |
FAM120C | ENSG00000184083.12 | transcript | ENST00000375180.7 | protein_coding | 12/15 | chrX | 54086647 | ||||||
chrX:54086754
|
C | CA | 170 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0022others(167): Show | 172 | HG00140.hp1 HG00558.hp1 HG00609.hp1 others(169): Show |
intron_variant | MODIFIER | c.2638-839dupT | FAM120C | ENSG00000184083.12 | transcript | ENST00000375180.7 | protein_coding | 12/15 | chrX | 54086754 | ||||||
chrX:54086754
|
C | CAA | 5 | a0001c0001t0011g0163a0001c0001t0011g0164a0001c0001t0026g0102others(2): Show | 5 | HG00280.hp1 HG01070.hp2 HG01074.hp1 others(2): Show |
intron_variant | MODIFIER | c.2638-840_2638-839d others(4): Show |
FAM120C | ENSG00000184083.12 | transcript | ENST00000375180.7 | protein_coding | 12/15 | chrX | 54086754 | ||||||
chrX:54086900
|
C | T | 4 | a0001c0001t0003g0040a0001c0001t0003g0041a0001c0001t0012g0127others(1): Show | 4 | NA18984.hp1 NA18994.hp1 NA19012.hp1 others(1): Show |
intron_variant | MODIFIER | c.2637+855G>A | FAM120C | ENSG00000184083.12 | transcript | ENST00000375180.7 | protein_coding | 12/15 | chrX | 54086900 | ||||||
chrX:54086902
|
C | CA | 1 | a0001c0001t0032g0108 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.2637+852dupT | FAM120C | ENSG00000184083.12 | transcript | ENST00000375180.7 | protein_coding | 12/15 | chrX | 54086902 | ||||||
chrX:54087295
|
G | T | 1 | a0001c0001t0003g0084 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.2637+460C>A | FAM120C | ENSG00000184083.12 | transcript | ENST00000375180.7 | protein_coding | 12/15 | chrX | 54087295 | ||||||
chrX:54087310
|
TA | T | 187 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0022others(184): Show | 189 | HG00140.hp1 HG00280.hp1 HG00558.hp1 others(186): Show |
intron_variant | MODIFIER | c.2637+444delT | FAM120C | ENSG00000184083.12 | transcript | ENST00000375180.7 | protein_coding | 12/15 | chrX | 54087310 | ||||||
chrX:54087390
|
CA | C | 1 | a0001c0005t0006g0004 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.2637+364delT | FAM120C | ENSG00000184083.12 | transcript | ENST00000375180.7 | protein_coding | 12/15 | chrX | 54087390 | ||||||
chrX:54087457
|
T | A | 3 | a0001c0001t0033g0012a0001c0001t0033g0013a0001c0001t0072g0106 | 3 | HG02559.hp2 HG02647.hp1 HG02809.hp1 |
intron_variant | MODIFIER | c.2637+298A>T | FAM120C | ENSG00000184083.12 | transcript | ENST00000375180.7 | protein_coding | 12/15 | chrX | 54087457 | ||||||
chrX:54087656
|
GC | G | 1 | a0005c0007t0034g0007 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.2637+98delG | FAM120C | ENSG00000184083.12 | transcript | ENST00000375180.7 | protein_coding | 12/15 | chrX | 54087656 | ||||||
chrX:54088355
|
G | A | 1 | a0002c0002t0047g0185 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.2428-391C>T | FAM120C | ENSG00000184083.12 | transcript | ENST00000375180.7 | protein_coding | 11/15 | chrX | 54088355 | ||||||
chrX:54088591
|
C | CA | 121 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0022others(118): Show | 122 | HG00140.hp1 HG00280.hp1 HG00558.hp1 others(119): Show |
intron_variant | MODIFIER | c.2428-628dupT | FAM120C | ENSG00000184083.12 | transcript | ENST00000375180.7 | protein_coding | 11/15 | chrX | 54088591 | ||||||
chrX:54088591
|
C | CAA | 16 | a0001c0001t0004g0006a0001c0001t0004g0071a0001c0001t0009g0070others(13): Show | 16 | HG01109.hp1 HG01261.hp1 HG02027.hp1 others(13): Show |
intron_variant | MODIFIER | c.2428-629_2428-628d others(4): Show |
FAM120C | ENSG00000184083.12 | transcript | ENST00000375180.7 | protein_coding | 11/15 | chrX | 54088591 | ||||||
chrX:54088874
|
C | T | 1 | a0001c0001t0067g0018 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.2428-910G>A | FAM120C | ENSG00000184083.12 | transcript | ENST00000375180.7 | protein_coding | 11/15 | chrX | 54088874 | ||||||
chrX:54089310
|
T | C | 1 | a0004c0008t0009g0105 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.2428-1346A>G | FAM120C | ENSG00000184083.12 | transcript | ENST00000375180.7 | protein_coding | 11/15 | chrX | 54089310 | ||||||
chrX:54089366
|
G | A | 2 | a0001c0001t0009g0034a0001c0001t0046g0085 | 2 | HG02056.hp1 HG02129.hp1 |
intron_variant | MODIFIER | c.2428-1402C>T | FAM120C | ENSG00000184083.12 | transcript | ENST00000375180.7 | protein_coding | 11/15 | chrX | 54089366 | ||||||
chrX:54089456
|
G | A | 47 | a0001c0001t0002g0132a0001c0001t0002g0153a0001c0001t0002g0159others(44): Show | 48 | HG00558.hp2 HG00609.hp1 HG00621.hp1 others(45): Show |
intron_variant | MODIFIER | c.2428-1492C>T | FAM120C | ENSG00000184083.12 | transcript | ENST00000375180.7 | protein_coding | 11/15 | chrX | 54089456 | ||||||
chrX:54089788
|
C | T | 34 | a0001c0001t0002g0132a0001c0001t0002g0153a0001c0001t0002g0159others(31): Show | 35 | HG00558.hp2 HG00609.hp1 HG00621.hp1 others(32): Show |
intron_variant | MODIFIER | c.2427+1524G>A | FAM120C | ENSG00000184083.12 | transcript | ENST00000375180.7 | protein_coding | 11/15 | chrX | 54089788 | ||||||
chrX:54089883
|
T | C | 187 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0022others(184): Show | 189 | HG00140.hp1 HG00280.hp1 HG00558.hp1 others(186): Show |
intron_variant | MODIFIER | c.2427+1429A>G | FAM120C | ENSG00000184083.12 | transcript | ENST00000375180.7 | protein_coding | 11/15 | chrX | 54089883 | ||||||
chrX:54089960
|
G | GA | 1 | a0001c0001t0074g0157 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.2427+1351dupT | FAM120C | ENSG00000184083.12 | transcript | ENST00000375180.7 | protein_coding | 11/15 | chrX | 54089960 | ||||||
chrX:54090239
|
C | CTTT | 3 | a0001c0001t0033g0012a0001c0001t0033g0013a0001c0001t0072g0106 | 3 | HG02559.hp2 HG02647.hp1 HG02809.hp1 |
intron_variant | MODIFIER | c.2427+1070_2427+107 others(7): Show |
FAM120C | ENSG00000184083.12 | transcript | ENST00000375180.7 | protein_coding | 11/15 | chrX | 54090239 | ||||||
chrX:54090239
|
C | CTTTT | 179 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0022others(176): Show | 181 | HG00140.hp1 HG00280.hp1 HG00558.hp1 others(178): Show |
intron_variant | MODIFIER | c.2427+1069_2427+107 others(8): Show |
FAM120C | ENSG00000184083.12 | transcript | ENST00000375180.7 | protein_coding | 11/15 | chrX | 54090239 | ||||||
chrX:54090239
|
C | CTTTTT | 5 | a0001c0001t0018g0115a0001c0001t0018g0116a0001c0001t0018g0151others(2): Show | 5 | HG02615.hp2 HG02809.hp2 HG06807.hp1 others(2): Show |
intron_variant | MODIFIER | c.2427+1068_2427+107 others(9): Show |
FAM120C | ENSG00000184083.12 | transcript | ENST00000375180.7 | protein_coding | 11/15 | chrX | 54090239 | ||||||
chrX:54091035
|
A | G | 1 | a0001c0001t0032g0108 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.2427+277T>C | FAM120C | ENSG00000184083.12 | transcript | ENST00000375180.7 | protein_coding | 11/15 | chrX | 54091035 | ||||||
chrX:54091142
|
G | A | 1 | a0001c0001t0072g0106 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.2427+170C>T | FAM120C | ENSG00000184083.12 | transcript | ENST00000375180.7 | protein_coding | 11/15 | chrX | 54091142 | ||||||
chrX:54091185
|
G | T | 1 | a0001c0001t0018g0151 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.2427+127C>A | FAM120C | ENSG00000184083.12 | transcript | ENST00000375180.7 | protein_coding | 11/15 | chrX | 54091185 | ||||||
chrX:54091307
|
C | A | 187 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0022others(184): Show | 189 | HG00140.hp1 HG00280.hp1 HG00558.hp1 others(186): Show |
splice_region_variant&intron_variant | LOW | c.2427+5G>T | FAM120C | ENSG00000184083.12 | transcript | ENST00000375180.7 | protein_coding | 11/15 | chrX | 54091307 | ||||||
chrX:54092740
|
ATTGT | A | 1 | a0001c0001t0015g0136 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.2313-1318_2313-131 others(8): Show |
FAM120C | ENSG00000184083.12 | transcript | ENST00000375180.7 | protein_coding | 10/15 | chrX | 54092740 | ||||||
chrX:54092747
|
CT | C | 1 | a0005c0007t0034g0007 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.2313-1322delA | FAM120C | ENSG00000184083.12 | transcript | ENST00000375180.7 | protein_coding | 10/15 | chrX | 54092747 | ||||||
chrX:54092962
|
TA | T | 1 | a0005c0007t0034g0007 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.2313-1537delT | FAM120C | ENSG00000184083.12 | transcript | ENST00000375180.7 | protein_coding | 10/15 | chrX | 54092962 | ||||||
chrX:54093213
|
CA | C | 1 | a0001c0001t0005g0062 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.2313-1788delT | FAM120C | ENSG00000184083.12 | transcript | ENST00000375180.7 | protein_coding | 10/15 | chrX | 54093213 | ||||||
chrX:54093533
|
C | T | 187 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0022others(184): Show | 189 | HG00140.hp1 HG00280.hp1 HG00558.hp1 others(186): Show |
intron_variant | MODIFIER | c.2313-2107G>A | FAM120C | ENSG00000184083.12 | transcript | ENST00000375180.7 | protein_coding | 10/15 | chrX | 54093533 | ||||||
chrX:54093583
|
G | A | 1 | a0001c0001t0009g0033 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.2313-2157C>T | FAM120C | ENSG00000184083.12 | transcript | ENST00000375180.7 | protein_coding | 10/15 | chrX | 54093583 | ||||||
chrX:54093597
|
A | G | 1 | a0001c0001t0028g0066 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.2313-2171T>C | FAM120C | ENSG00000184083.12 | transcript | ENST00000375180.7 | protein_coding | 10/15 | chrX | 54093597 | ||||||
chrX:54094083
|
C | CCT | 1 | a0001c0001t0005g0062 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.2313-2658_2313-265 others(6): Show |
FAM120C | ENSG00000184083.12 | transcript | ENST00000375180.7 | protein_coding | 10/15 | chrX | 54094083 | ||||||
chrX:54094083
|
C | CT | 109 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0022others(106): Show | 110 | HG00140.hp1 HG00280.hp1 HG00558.hp1 others(107): Show |
intron_variant | MODIFIER | c.2313-2658dupA | FAM120C | ENSG00000184083.12 | transcript | ENST00000375180.7 | protein_coding | 10/15 | chrX | 54094083 | ||||||
chrX:54094083
|
C | CTT | 22 | a0001c0001t0001g0042a0001c0001t0001g0060a0001c0001t0003g0038others(19): Show | 22 | HG00642.hp1 HG01106.hp1 HG01109.hp1 others(19): Show |
intron_variant | MODIFIER | c.2313-2659_2313-265 others(6): Show |
FAM120C | ENSG00000184083.12 | transcript | ENST00000375180.7 | protein_coding | 10/15 | chrX | 54094083 | ||||||
chrX:54094083
|
C | CTTT | 1 | a0001c0001t0021g0014 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.2313-2660_2313-265 others(7): Show |
FAM120C | ENSG00000184083.12 | transcript | ENST00000375180.7 | protein_coding | 10/15 | chrX | 54094083 | ||||||
chrX:54094083
|
CT | C | 2 | a0001c0001t0013g0130a0001c0001t0049g0152 | 2 | HG02572.hp1 HG02896.hp2 |
intron_variant | MODIFIER | c.2313-2658delA | FAM120C | ENSG00000184083.12 | transcript | ENST00000375180.7 | protein_coding | 10/15 | chrX | 54094083 | ||||||
chrX:54094154
|
G | C | 1 | a0001c0001t0061g0019 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.2313-2728C>G | FAM120C | ENSG00000184083.12 | transcript | ENST00000375180.7 | protein_coding | 10/15 | chrX | 54094154 | ||||||
chrX:54094254
|
C | T | 2 | a0001c0001t0017g0005a0001c0001t0017g0171 | 2 | HG01167.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.2313-2828G>A | FAM120C | ENSG00000184083.12 | transcript | ENST00000375180.7 | protein_coding | 10/15 | chrX | 54094254 | ||||||
chrX:54094904
|
CA | C | 176 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0022others(173): Show | 178 | HG00140.hp1 HG00280.hp1 HG00558.hp1 others(175): Show |
intron_variant | MODIFIER | c.2313-3479delT | FAM120C | ENSG00000184083.12 | transcript | ENST00000375180.7 | protein_coding | 10/15 | chrX | 54094904 | ||||||
chrX:54094904
|
CAA | C | 8 | a0001c0001t0002g0132a0001c0001t0008g0124a0001c0001t0008g0125others(5): Show | 8 | HG01081.hp1 HG02258.hp1 HG02451.hp1 others(5): Show |
intron_variant | MODIFIER | c.2313-3480_2313-347 others(6): Show |
FAM120C | ENSG00000184083.12 | transcript | ENST00000375180.7 | protein_coding | 10/15 | chrX | 54094904 | ||||||
chrX:54095067
|
A | AAAAAC | 10 | a0001c0001t0003g0087a0001c0001t0004g0069a0001c0001t0004g0071others(7): Show | 10 | HG00140.hp1 HG01099.hp1 HG01169.hp2 others(7): Show |
intron_variant | MODIFIER | c.2313-3646_2313-364 others(9): Show |
FAM120C | ENSG00000184083.12 | transcript | ENST00000375180.7 | protein_coding | 10/15 | chrX | 54095067 | ||||||
chrX:54095290
|
A | G | 1 | a0001c0001t0036g0078 | 1 | HG01169.hp2 | intron_variant | MODIFIER | c.2313-3864T>C | FAM120C | ENSG00000184083.12 | transcript | ENST00000375180.7 | protein_coding | 10/15 | chrX | 54095290 | ||||||
chrX:54095355
|
CT | C | 169 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0022others(166): Show | 171 | HG00140.hp1 HG00280.hp1 HG00558.hp1 others(168): Show |
intron_variant | MODIFIER | c.2313-3930delA | FAM120C | ENSG00000184083.12 | transcript | ENST00000375180.7 | protein_coding | 10/15 | chrX | 54095355 | ||||||
chrX:54095355
|
CTT | C | 5 | a0001c0001t0009g0049a0001c0001t0012g0127a0001c0001t0015g0136others(2): Show | 5 | HG02895.hp1 HG02896.hp1 NA18984.hp1 others(2): Show |
intron_variant | MODIFIER | c.2313-3931_2313-393 others(6): Show |
FAM120C | ENSG00000184083.12 | transcript | ENST00000375180.7 | protein_coding | 10/15 | chrX | 54095355 | ||||||
chrX:54095375
|
TTG | T | 1 | a0001c0001t0005g0062 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.2313-3951_2313-395 others(6): Show |
FAM120C | ENSG00000184083.12 | transcript | ENST00000375180.7 | protein_coding | 10/15 | chrX | 54095375 | ||||||
chrX:54095407
|
C | T | 2 | a0001c0001t0013g0112a0001c0001t0019g0111 | 2 | HG02630.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.2313-3981G>A | FAM120C | ENSG00000184083.12 | transcript | ENST00000375180.7 | protein_coding | 10/15 | chrX | 54095407 | ||||||
chrX:54095520
|
AT | A | 1 | a0001c0001t0005g0062 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.2313-4095delA | FAM120C | ENSG00000184083.12 | transcript | ENST00000375180.7 | protein_coding | 10/15 | chrX | 54095520 | ||||||
chrX:54095623
|
AG | A | 1 | a0001c0001t0005g0062 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.2313-4198delC | FAM120C | ENSG00000184083.12 | transcript | ENST00000375180.7 | protein_coding | 10/15 | chrX | 54095623 | ||||||
chrX:54095660
|
TTG | T | 1 | a0001c0001t0005g0062 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.2313-4236_2313-423 others(6): Show |
FAM120C | ENSG00000184083.12 | transcript | ENST00000375180.7 | protein_coding | 10/15 | chrX | 54095660 | ||||||
chrX:54095704
|
TG | T | 1 | a0001c0001t0005g0062 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.2313-4279delC | FAM120C | ENSG00000184083.12 | transcript | ENST00000375180.7 | protein_coding | 10/15 | chrX | 54095704 | ||||||
chrX:54095727
|
G | GC | 1 | a0001c0001t0005g0113 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.2313-4302dupG | FAM120C | ENSG00000184083.12 | transcript | ENST00000375180.7 | protein_coding | 10/15 | chrX | 54095727 | ||||||
chrX:54095797
|
C | T | 1 | a0001c0001t0002g0168 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.2313-4371G>A | FAM120C | ENSG00000184083.12 | transcript | ENST00000375180.7 | protein_coding | 10/15 | chrX | 54095797 | ||||||
chrX:54095907
|
CG | C | 1 | a0001c0001t0005g0062 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.2313-4482delC | FAM120C | ENSG00000184083.12 | transcript | ENST00000375180.7 | protein_coding | 10/15 | chrX | 54095907 | ||||||
chrX:54095915
|
CA | C | 1 | a0001c0001t0005g0062 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.2313-4490delT | FAM120C | ENSG00000184083.12 | transcript | ENST00000375180.7 | protein_coding | 10/15 | chrX | 54095915 | ||||||
chrX:54095923
|
TG | T | 1 | a0001c0001t0005g0062 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.2313-4498delC | FAM120C | ENSG00000184083.12 | transcript | ENST00000375180.7 | protein_coding | 10/15 | chrX | 54095923 | ||||||
chrX:54095969
|
T | TTAAATAA others(2): Show |
1 | a0005c0007t0034g0007 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.2313-4552_2313-454 others(13): Show |
FAM120C | ENSG00000184083.12 | transcript | ENST00000375180.7 | protein_coding | 10/15 | chrX | 54095969 | ||||||
chrX:54096065
|
T | TA | 1 | a0001c0001t0005g0113 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.2313-4640dupT | FAM120C | ENSG00000184083.12 | transcript | ENST00000375180.7 | protein_coding | 10/15 | chrX | 54096065 | ||||||
chrX:54096066
|
A | T | 1 | a0001c0001t0005g0062 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.2313-4640T>A | FAM120C | ENSG00000184083.12 | transcript | ENST00000375180.7 | protein_coding | 10/15 | chrX | 54096066 | ||||||
chrX:54096085
|
TG | T | 1 | a0001c0001t0005g0062 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.2313-4660delC | FAM120C | ENSG00000184083.12 | transcript | ENST00000375180.7 | protein_coding | 10/15 | chrX | 54096085 | ||||||
chrX:54096227
|
A | G | 1 | a0001c0001t0015g0097 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.2313-4801T>C | FAM120C | ENSG00000184083.12 | transcript | ENST00000375180.7 | protein_coding | 10/15 | chrX | 54096227 | ||||||
chrX:54096256
|
C | A | 1 | a0001c0001t0003g0087 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.2313-4830G>T | FAM120C | ENSG00000184083.12 | transcript | ENST00000375180.7 | protein_coding | 10/15 | chrX | 54096256 | ||||||
chrX:54096257
|
A | AG | 1 | a0001c0001t0005g0062 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.2313-4832_2313-483 others(5): Show |
FAM120C | ENSG00000184083.12 | transcript | ENST00000375180.7 | protein_coding | 10/15 | chrX | 54096257 | ||||||
chrX:54096316
|
TG | T | 1 | a0001c0001t0005g0062 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.2313-4891delC | FAM120C | ENSG00000184083.12 | transcript | ENST00000375180.7 | protein_coding | 10/15 | chrX | 54096316 | ||||||
chrX:54096418
|
TA | T | 1 | a0001c0001t0005g0062 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.2313-4993delT | FAM120C | ENSG00000184083.12 | transcript | ENST00000375180.7 | protein_coding | 10/15 | chrX | 54096418 | ||||||
chrX:54096594
|
CT | C | 1 | a0001c0001t0005g0062 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.2313-5169delA | FAM120C | ENSG00000184083.12 | transcript | ENST00000375180.7 | protein_coding | 10/15 | chrX | 54096594 | ||||||
chrX:54096612
|
CT | C | 1 | a0001c0001t0005g0062 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.2313-5187delA | FAM120C | ENSG00000184083.12 | transcript | ENST00000375180.7 | protein_coding | 10/15 | chrX | 54096612 | ||||||
chrX:54096796
|
A | T | 4 | a0001c0001t0003g0040a0001c0001t0003g0041a0001c0001t0012g0127others(1): Show | 4 | NA18984.hp1 NA18994.hp1 NA19012.hp1 others(1): Show |
intron_variant | MODIFIER | c.2313-5370T>A | FAM120C | ENSG00000184083.12 | transcript | ENST00000375180.7 | protein_coding | 10/15 | chrX | 54096796 | ||||||
chrX:54096833
|
T | A | 1 | a0001c0001t0022g0149 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.2313-5407A>T | FAM120C | ENSG00000184083.12 | transcript | ENST00000375180.7 | protein_coding | 10/15 | chrX | 54096833 | ||||||
chrX:54096975
|
T | C | 1 | a0001c0001t0009g0049 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.2313-5549A>G | FAM120C | ENSG00000184083.12 | transcript | ENST00000375180.7 | protein_coding | 10/15 | chrX | 54096975 | ||||||
chrX:54097077
|
AT | A | 1 | a0001c0001t0005g0062 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.2313-5652delA | FAM120C | ENSG00000184083.12 | transcript | ENST00000375180.7 | protein_coding | 10/15 | chrX | 54097077 | ||||||
chrX:54097107
|
AG | A | 1 | a0001c0001t0005g0062 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.2313-5682delC | FAM120C | ENSG00000184083.12 | transcript | ENST00000375180.7 | protein_coding | 10/15 | chrX | 54097107 | ||||||
chrX:54097258
|
C | T | 2 | a0001c0001t0015g0015a0001c0001t0022g0016 | 2 | HG01884.hp1 HG02717.hp1 |
intron_variant | MODIFIER | c.2313-5832G>A | FAM120C | ENSG00000184083.12 | transcript | ENST00000375180.7 | protein_coding | 10/15 | chrX | 54097258 | ||||||
chrX:54097376
|
GC | G | 1 | a0001c0001t0005g0062 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.2313-5951delG | FAM120C | ENSG00000184083.12 | transcript | ENST00000375180.7 | protein_coding | 10/15 | chrX | 54097376 | ||||||
chrX:54097442
|
TA | T | 1 | a0001c0001t0005g0062 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.2313-6017delT | FAM120C | ENSG00000184083.12 | transcript | ENST00000375180.7 | protein_coding | 10/15 | chrX | 54097442 | ||||||
chrX:54097461
|
CGA | C | 1 | a0005c0007t0034g0007 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.2313-6037_2313-603 others(6): Show |
FAM120C | ENSG00000184083.12 | transcript | ENST00000375180.7 | protein_coding | 10/15 | chrX | 54097461 | ||||||
chrX:54097692
|
CT | C | 1 | a0001c0001t0005g0062 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.2313-6267delA | FAM120C | ENSG00000184083.12 | transcript | ENST00000375180.7 | protein_coding | 10/15 | chrX | 54097692 | ||||||
chrX:54097706
|
G | C | 1 | a0001c0001t0001g0008 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.2313-6280C>G | FAM120C | ENSG00000184083.12 | transcript | ENST00000375180.7 | protein_coding | 10/15 | chrX | 54097706 | ||||||
chrX:54097828
|
G | A | 5 | a0001c0001t0002g0132a0001c0001t0008g0124a0001c0001t0008g0125others(2): Show | 5 | HG01081.hp1 HG02258.hp1 HG02451.hp1 others(2): Show |
intron_variant | MODIFIER | c.2313-6402C>T | FAM120C | ENSG00000184083.12 | transcript | ENST00000375180.7 | protein_coding | 10/15 | chrX | 54097828 | ||||||
chrX:54097919
|
G | A | 5 | a0001c0001t0002g0132a0001c0001t0008g0124a0001c0001t0008g0125others(2): Show | 5 | HG01081.hp1 HG02258.hp1 HG02451.hp1 others(2): Show |
intron_variant | MODIFIER | c.2313-6493C>T | FAM120C | ENSG00000184083.12 | transcript | ENST00000375180.7 | protein_coding | 10/15 | chrX | 54097919 | ||||||
chrX:54097931
|
T | G | 1 | a0001c0001t0041g0098 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.2313-6505A>C | FAM120C | ENSG00000184083.12 | transcript | ENST00000375180.7 | protein_coding | 10/15 | chrX | 54097931 | ||||||
chrX:54098017
|
T | C | 187 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0022others(184): Show | 189 | HG00140.hp1 HG00280.hp1 HG00558.hp1 others(186): Show |
intron_variant | MODIFIER | c.2313-6591A>G | FAM120C | ENSG00000184083.12 | transcript | ENST00000375180.7 | protein_coding | 10/15 | chrX | 54098017 | ||||||
chrX:54098022
|
G | A | 1 | a0004c0008t0009g0105 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.2313-6596C>T | FAM120C | ENSG00000184083.12 | transcript | ENST00000375180.7 | protein_coding | 10/15 | chrX | 54098022 | ||||||
chrX:54098041
|
C | CT | 4 | a0001c0001t0001g0008a0001c0001t0005g0011a0001c0001t0008g0165others(1): Show | 4 | HG02074.hp1 NA19077.hp1 NA19077.hp2 others(1): Show |
intron_variant | MODIFIER | c.2313-6616dupA | FAM120C | ENSG00000184083.12 | transcript | ENST00000375180.7 | protein_coding | 10/15 | chrX | 54098041 | ||||||
chrX:54098041
|
CT | C | 6 | a0001c0001t0002g0132a0001c0001t0005g0059a0001c0001t0009g0073others(3): Show | 6 | HG00558.hp1 HG01081.hp1 HG01515.hp1 others(3): Show |
intron_variant | MODIFIER | c.2313-6616delA | FAM120C | ENSG00000184083.12 | transcript | ENST00000375180.7 | protein_coding | 10/15 | chrX | 54098041 | ||||||
chrX:54098101
|
A | G | 1 | a0001c0001t0072g0106 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.2313-6675T>C | FAM120C | ENSG00000184083.12 | transcript | ENST00000375180.7 | protein_coding | 10/15 | chrX | 54098101 | ||||||
chrX:54098172
|
GC | G | 1 | a0001c0001t0018g0151 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.2313-6747delG | FAM120C | ENSG00000184083.12 | transcript | ENST00000375180.7 | protein_coding | 10/15 | chrX | 54098172 | ||||||
chrX:54098334
|
C | T | 1 | a0001c0001t0073g0179 | 1 | NA19078.hp1 | intron_variant | MODIFIER | c.2313-6908G>A | FAM120C | ENSG00000184083.12 | transcript | ENST00000375180.7 | protein_coding | 10/15 | chrX | 54098334 | ||||||
chrX:54098336
|
CG | C | 1 | a0005c0007t0034g0007 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.2313-6911delC | FAM120C | ENSG00000184083.12 | transcript | ENST00000375180.7 | protein_coding | 10/15 | chrX | 54098336 | ||||||
chrX:54098431
|
GT | G | 1 | a0005c0007t0034g0007 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.2313-7006delA | FAM120C | ENSG00000184083.12 | transcript | ENST00000375180.7 | protein_coding | 10/15 | chrX | 54098431 | ||||||
chrX:54098475
|
CT | C | 1 | a0001c0001t0012g0043 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.2313-7050delA | FAM120C | ENSG00000184083.12 | transcript | ENST00000375180.7 | protein_coding | 10/15 | chrX | 54098475 | ||||||
chrX:54098492
|
C | G | 2 | a0001c0001t0033g0012a0001c0001t0033g0013 | 2 | HG02559.hp2 HG02647.hp1 |
intron_variant | MODIFIER | c.2313-7066G>C | FAM120C | ENSG00000184083.12 | transcript | ENST00000375180.7 | protein_coding | 10/15 | chrX | 54098492 | ||||||
chrX:54098494
|
G | A | 2 | a0001c0001t0063g0009a0001c0001t0073g0179 | 2 | NA18962.hp1 NA19078.hp1 |
intron_variant | MODIFIER | c.2313-7068C>T | FAM120C | ENSG00000184083.12 | transcript | ENST00000375180.7 | protein_coding | 10/15 | chrX | 54098494 | ||||||
chrX:54098617
|
T | A | 1 | a0001c0001t0022g0149 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.2313-7191A>T | FAM120C | ENSG00000184083.12 | transcript | ENST00000375180.7 | protein_coding | 10/15 | chrX | 54098617 | ||||||
chrX:54098771
|
G | A | 6 | a0001c0001t0015g0015a0001c0001t0022g0016a0001c0001t0026g0101others(3): Show | 6 | HG00735.hp1 HG01243.hp1 HG01884.hp1 others(3): Show |
intron_variant | MODIFIER | c.2313-7345C>T | FAM120C | ENSG00000184083.12 | transcript | ENST00000375180.7 | protein_coding | 10/15 | chrX | 54098771 | ||||||
chrX:54098783
|
G | GC | 1 | a0005c0007t0034g0007 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.2313-7358dupG | FAM120C | ENSG00000184083.12 | transcript | ENST00000375180.7 | protein_coding | 10/15 | chrX | 54098783 | ||||||
chrX:54098870
|
CG | C | 1 | a0005c0007t0034g0007 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.2313-7445delC | FAM120C | ENSG00000184083.12 | transcript | ENST00000375180.7 | protein_coding | 10/15 | chrX | 54098870 | ||||||
chrX:54098917
|
C | G | 1 | a0001c0001t0067g0018 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.2313-7491G>C | FAM120C | ENSG00000184083.12 | transcript | ENST00000375180.7 | protein_coding | 10/15 | chrX | 54098917 | ||||||
chrX:54099013
|
CT | C | 167 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0022others(164): Show | 169 | HG00140.hp1 HG00280.hp1 HG00558.hp1 others(166): Show |
intron_variant | MODIFIER | c.2313-7588delA | FAM120C | ENSG00000184083.12 | transcript | ENST00000375180.7 | protein_coding | 10/15 | chrX | 54099013 | ||||||
chrX:54099013
|
CTT | C | 4 | a0001c0001t0003g0181a0001c0001t0009g0073a0001c0001t0021g0077others(1): Show | 4 | HG01106.hp1 NA18982.hp1 NA19056.hp1 others(1): Show |
intron_variant | MODIFIER | c.2313-7589_2313-758 others(6): Show |
FAM120C | ENSG00000184083.12 | transcript | ENST00000375180.7 | protein_coding | 10/15 | chrX | 54099013 | ||||||
chrX:54099123
|
TC | T | 1 | a0005c0007t0034g0007 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.2313-7698delG | FAM120C | ENSG00000184083.12 | transcript | ENST00000375180.7 | protein_coding | 10/15 | chrX | 54099123 | ||||||
chrX:54099389
|
G | C | 1 | a0002c0002t0019g0186 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.2313-7963C>G | FAM120C | ENSG00000184083.12 | transcript | ENST00000375180.7 | protein_coding | 10/15 | chrX | 54099389 | ||||||
chrX:54099571
|
G | A | 187 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0022others(184): Show | 189 | HG00140.hp1 HG00280.hp1 HG00558.hp1 others(186): Show |
intron_variant | MODIFIER | c.2313-8145C>T | FAM120C | ENSG00000184083.12 | transcript | ENST00000375180.7 | protein_coding | 10/15 | chrX | 54099571 | ||||||
chrX:54099685
|
C | CT | 1 | a0001c0001t0062g0182 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.2313-8260dupA | FAM120C | ENSG00000184083.12 | transcript | ENST00000375180.7 | protein_coding | 10/15 | chrX | 54099685 | ||||||
chrX:54100062
|
T | C | 1 | a0001c0001t0049g0152 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.2313-8636A>G | FAM120C | ENSG00000184083.12 | transcript | ENST00000375180.7 | protein_coding | 10/15 | chrX | 54100062 | ||||||
chrX:54100126
|
G | A | 6 | a0001c0001t0018g0115a0001c0001t0018g0116a0001c0001t0018g0151others(3): Show | 6 | HG02572.hp1 HG02615.hp2 HG02809.hp2 others(3): Show |
intron_variant | MODIFIER | c.2313-8700C>T | FAM120C | ENSG00000184083.12 | transcript | ENST00000375180.7 | protein_coding | 10/15 | chrX | 54100126 | ||||||
chrX:54100277
|
G | C | 2 | a0001c0001t0017g0005a0001c0001t0017g0171 | 2 | HG01167.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.2313-8851C>G | FAM120C | ENSG00000184083.12 | transcript | ENST00000375180.7 | protein_coding | 10/15 | chrX | 54100277 | ||||||
chrX:54100335
|
C | CA | 1 | a0001c0001t0063g0009 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.2313-8910dupT | FAM120C | ENSG00000184083.12 | transcript | ENST00000375180.7 | protein_coding | 10/15 | chrX | 54100335 | ||||||
chrX:54100374
|
TC | T | 1 | a0001c0001t0066g0076 | 1 | NA19089.hp1 | intron_variant | MODIFIER | c.2313-8949delG | FAM120C | ENSG00000184083.12 | transcript | ENST00000375180.7 | protein_coding | 10/15 | chrX | 54100374 | ||||||
chrX:54100385
|
CG | C | 1 | a0005c0007t0034g0007 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.2313-8960delC | FAM120C | ENSG00000184083.12 | transcript | ENST00000375180.7 | protein_coding | 10/15 | chrX | 54100385 | ||||||
chrX:54100386
|
G | A | 1 | a0001c0001t0007g0054 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.2313-8960C>T | FAM120C | ENSG00000184083.12 | transcript | ENST00000375180.7 | protein_coding | 10/15 | chrX | 54100386 | ||||||
chrX:54100522
|
A | G | 1 | a0001c0001t0020g0002 | 2 | HG01934.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.2313-9096T>C | FAM120C | ENSG00000184083.12 | transcript | ENST00000375180.7 | protein_coding | 10/15 | chrX | 54100522 | ||||||
chrX:54100535
|
T | C | 32 | a0001c0001t0001g0022a0001c0001t0001g0060a0001c0001t0001g0061others(29): Show | 32 | HG00280.hp1 HG00558.hp1 HG00642.hp1 others(29): Show |
intron_variant | MODIFIER | c.2313-9109A>G | FAM120C | ENSG00000184083.12 | transcript | ENST00000375180.7 | protein_coding | 10/15 | chrX | 54100535 | ||||||
chrX:54100656
|
AAAAC | A | 2 | a0001c0001t0010g0175a0001c0001t0011g0010 | 2 | NA18980.hp1 NA18980.hp2 |
intron_variant | MODIFIER | c.2313-9234_2313-923 others(8): Show |
FAM120C | ENSG00000184083.12 | transcript | ENST00000375180.7 | protein_coding | 10/15 | chrX | 54100656 | ||||||
chrX:54101135
|
C | T | 2 | a0001c0001t0014g0093a0001c0001t0014g0094 | 2 | HG02602.hp1 HG02735.hp1 |
intron_variant | MODIFIER | c.2313-9709G>A | FAM120C | ENSG00000184083.12 | transcript | ENST00000375180.7 | protein_coding | 10/15 | chrX | 54101135 | ||||||
chrX:54101135
|
CG | C | 1 | a0005c0007t0034g0007 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.2313-9710delC | FAM120C | ENSG00000184083.12 | transcript | ENST00000375180.7 | protein_coding | 10/15 | chrX | 54101135 | ||||||
chrX:54101209
|
C | A | 1 | a0001c0001t0055g0048 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.2313-9783G>T | FAM120C | ENSG00000184083.12 | transcript | ENST00000375180.7 | protein_coding | 10/15 | chrX | 54101209 | ||||||
chrX:54101430
|
TG | T | 1 | a0005c0007t0034g0007 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.2313-10005delC | FAM120C | ENSG00000184083.12 | transcript | ENST00000375180.7 | protein_coding | 10/15 | chrX | 54101430 | ||||||
chrX:54101922
|
C | G | 6 | a0001c0001t0018g0115a0001c0001t0018g0116a0001c0001t0018g0151others(3): Show | 6 | HG02572.hp1 HG02615.hp2 HG02809.hp2 others(3): Show |
intron_variant | MODIFIER | c.2313-10496G>C | FAM120C | ENSG00000184083.12 | transcript | ENST00000375180.7 | protein_coding | 10/15 | chrX | 54101922 | ||||||
chrX:54102023
|
A | C | 184 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0022others(181): Show | 186 | HG00140.hp1 HG00280.hp1 HG00558.hp1 others(183): Show |
intron_variant | MODIFIER | c.2313-10597T>G | FAM120C | ENSG00000184083.12 | transcript | ENST00000375180.7 | protein_coding | 10/15 | chrX | 54102023 | ||||||
chrX:54102038
|
CT | C | 1 | a0001c0005t0006g0004 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.2313-10613delA | FAM120C | ENSG00000184083.12 | transcript | ENST00000375180.7 | protein_coding | 10/15 | chrX | 54102038 | ||||||
chrX:54102151
|
CG | C | 1 | a0005c0007t0034g0007 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.2313-10726delC | FAM120C | ENSG00000184083.12 | transcript | ENST00000375180.7 | protein_coding | 10/15 | chrX | 54102151 | ||||||
chrX:54102179
|
T | G | 6 | a0001c0001t0001g0044a0001c0001t0001g0079a0001c0001t0006g0030others(3): Show | 6 | HG02698.hp1 HG02738.hp1 HG04204.hp1 others(3): Show |
intron_variant | MODIFIER | c.2313-10753A>C | FAM120C | ENSG00000184083.12 | transcript | ENST00000375180.7 | protein_coding | 10/15 | chrX | 54102179 | ||||||
chrX:54102236
|
A | C | 23 | a0001c0001t0013g0112a0001c0001t0015g0015a0001c0001t0015g0097others(20): Show | 23 | HG00735.hp1 HG00738.hp1 HG01243.hp1 others(20): Show |
intron_variant | MODIFIER | c.2313-10810T>G | FAM120C | ENSG00000184083.12 | transcript | ENST00000375180.7 | protein_coding | 10/15 | chrX | 54102236 | ||||||
chrX:54102250
|
T | C | 155 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0022others(152): Show | 157 | HG00140.hp1 HG00280.hp1 HG00558.hp1 others(154): Show |
intron_variant | MODIFIER | c.2313-10824A>G | FAM120C | ENSG00000184083.12 | transcript | ENST00000375180.7 | protein_coding | 10/15 | chrX | 54102250 | ||||||
chrX:54102280
|
TG | T | 1 | a0005c0007t0034g0007 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.2313-10855delC | FAM120C | ENSG00000184083.12 | transcript | ENST00000375180.7 | protein_coding | 10/15 | chrX | 54102280 | ||||||
chrX:54102326
|
G | A | 1 | a0001c0001t0074g0157 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.2313-10900C>T | FAM120C | ENSG00000184083.12 | transcript | ENST00000375180.7 | protein_coding | 10/15 | chrX | 54102326 | ||||||
chrX:54102609
|
AGAT | A | 1 | a0001c0001t0001g0036 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.2313-11186_2313-11 others(9): Show |
FAM120C | ENSG00000184083.12 | transcript | ENST00000375180.7 | protein_coding | 10/15 | chrX | 54102609 | ||||||
chrX:54102661
|
T | G | 2 | a0001c0001t0058g0020a0001c0001t0061g0019 | 2 | HG01069.hp1 HG01952.hp1 |
intron_variant | MODIFIER | c.2313-11235A>C | FAM120C | ENSG00000184083.12 | transcript | ENST00000375180.7 | protein_coding | 10/15 | chrX | 54102661 | ||||||
chrX:54102724
|
G | GT | 4 | a0001c0001t0009g0073a0001c0001t0013g0130a0001c0001t0053g0099others(1): Show | 4 | HG00735.hp1 HG02896.hp2 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.2313-11299dupA | FAM120C | ENSG00000184083.12 | transcript | ENST00000375180.7 | protein_coding | 10/15 | chrX | 54102724 | ||||||
chrX:54102724
|
GT | G | 10 | a0001c0001t0006g0026a0001c0001t0006g0028a0001c0001t0006g0029others(7): Show | 10 | NA18955.hp1 NA18959.hp1 NA18965.hp1 others(7): Show |
intron_variant | MODIFIER | c.2313-11299delA | FAM120C | ENSG00000184083.12 | transcript | ENST00000375180.7 | protein_coding | 10/15 | chrX | 54102724 | ||||||
chrX:54102782
|
C | T | 1 | a0006c0006t0001g0128 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.2313-11356G>A | FAM120C | ENSG00000184083.12 | transcript | ENST00000375180.7 | protein_coding | 10/15 | chrX | 54102782 | ||||||
chrX:54103230
|
AT | A | 1 | a0001c0001t0005g0062 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.2313-11805delA | FAM120C | ENSG00000184083.12 | transcript | ENST00000375180.7 | protein_coding | 10/15 | chrX | 54103230 | ||||||
chrX:54103326
|
C | CAAT | 1 | a0002c0002t0019g0186 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.2313-11903_2313-11 others(9): Show |
FAM120C | ENSG00000184083.12 | transcript | ENST00000375180.7 | protein_coding | 10/15 | chrX | 54103326 | ||||||
chrX:54103405
|
C | T | 2 | a0001c0001t0043g0147a0001c0001t0045g0148 | 2 | HG02922.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.2313-11979G>A | FAM120C | ENSG00000184083.12 | transcript | ENST00000375180.7 | protein_coding | 10/15 | chrX | 54103405 | ||||||
chrX:54103497
|
T | C | 3 | a0001c0001t0033g0012a0001c0001t0033g0013a0001c0001t0072g0106 | 3 | HG02559.hp2 HG02647.hp1 HG02809.hp1 |
intron_variant | MODIFIER | c.2313-12071A>G | FAM120C | ENSG00000184083.12 | transcript | ENST00000375180.7 | protein_coding | 10/15 | chrX | 54103497 | ||||||
chrX:54103622
|
G | GT | 1 | a0001c0001t0013g0130 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.2313-12197dupA | FAM120C | ENSG00000184083.12 | transcript | ENST00000375180.7 | protein_coding | 10/15 | chrX | 54103622 | ||||||
chrX:54103638
|
G | A | 1 | a0001c0001t0013g0130 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.2313-12212C>T | FAM120C | ENSG00000184083.12 | transcript | ENST00000375180.7 | protein_coding | 10/15 | chrX | 54103638 | ||||||
chrX:54103755
|
C | CT | 2 | a0001c0001t0067g0018a0001c0001t0072g0106 | 2 | HG02257.hp1 HG02809.hp1 |
intron_variant | MODIFIER | c.2313-12330dupA | FAM120C | ENSG00000184083.12 | transcript | ENST00000375180.7 | protein_coding | 10/15 | chrX | 54103755 | ||||||
chrX:54103755
|
CT | C | 177 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0022others(174): Show | 179 | HG00140.hp1 HG00280.hp1 HG00558.hp1 others(176): Show |
intron_variant | MODIFIER | c.2313-12330delA | FAM120C | ENSG00000184083.12 | transcript | ENST00000375180.7 | protein_coding | 10/15 | chrX | 54103755 | ||||||
chrX:54104289
|
G | C | 1 | a0001c0001t0041g0098 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.2312+12256C>G | FAM120C | ENSG00000184083.12 | transcript | ENST00000375180.7 | protein_coding | 10/15 | chrX | 54104289 | ||||||
chrX:54104513
|
T | TA | 1 | a0001c0001t0005g0062 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.2312+12031dupT | FAM120C | ENSG00000184083.12 | transcript | ENST00000375180.7 | protein_coding | 10/15 | chrX | 54104513 | ||||||
chrX:54104543
|
C | CG | 1 | a0001c0001t0005g0062 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.2312+12001_2312+12 others(7): Show |
FAM120C | ENSG00000184083.12 | transcript | ENST00000375180.7 | protein_coding | 10/15 | chrX | 54104543 | ||||||
chrX:54104569
|
AG | A | 1 | a0001c0001t0005g0062 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.2312+11975delC | FAM120C | ENSG00000184083.12 | transcript | ENST00000375180.7 | protein_coding | 10/15 | chrX | 54104569 | ||||||
chrX:54104578
|
C | CG | 1 | a0001c0001t0001g0036 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.2312+11966dupC | FAM120C | ENSG00000184083.12 | transcript | ENST00000375180.7 | protein_coding | 10/15 | chrX | 54104578 | ||||||
chrX:54104628
|
C | T | 178 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0022others(175): Show | 180 | HG00140.hp1 HG00280.hp1 HG00558.hp1 others(177): Show |
intron_variant | MODIFIER | c.2312+11917G>A | FAM120C | ENSG00000184083.12 | transcript | ENST00000375180.7 | protein_coding | 10/15 | chrX | 54104628 | ||||||
chrX:54104739
|
CG | C | 1 | a0001c0001t0005g0062 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.2312+11805delC | FAM120C | ENSG00000184083.12 | transcript | ENST00000375180.7 | protein_coding | 10/15 | chrX | 54104739 | ||||||
chrX:54104807
|
C | CG | 7 | a0001c0001t0003g0032a0001c0001t0003g0040a0001c0001t0012g0104others(4): Show | 7 | HG02083.hp1 HG02559.hp2 HG02647.hp1 others(4): Show |
intron_variant | MODIFIER | c.2312+11737dupC | FAM120C | ENSG00000184083.12 | transcript | ENST00000375180.7 | protein_coding | 10/15 | chrX | 54104807 | ||||||
chrX:54104815
|
G | GA | 1 | a0001c0001t0006g0030 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.2312+11729dupT | FAM120C | ENSG00000184083.12 | transcript | ENST00000375180.7 | protein_coding | 10/15 | chrX | 54104815 | ||||||
chrX:54105061
|
G | A | 1 | a0001c0001t0014g0075 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.2312+11484C>T | FAM120C | ENSG00000184083.12 | transcript | ENST00000375180.7 | protein_coding | 10/15 | chrX | 54105061 | ||||||
chrX:54105143
|
G | A | 1 | a0001c0001t0013g0130 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.2312+11402C>T | FAM120C | ENSG00000184083.12 | transcript | ENST00000375180.7 | protein_coding | 10/15 | chrX | 54105143 | ||||||
chrX:54105168
|
T | C | 6 | a0001c0001t0018g0115a0001c0001t0018g0116a0001c0001t0018g0151others(3): Show | 6 | HG02572.hp1 HG02615.hp2 HG02809.hp2 others(3): Show |
intron_variant | MODIFIER | c.2312+11377A>G | FAM120C | ENSG00000184083.12 | transcript | ENST00000375180.7 | protein_coding | 10/15 | chrX | 54105168 | ||||||
chrX:54105360
|
C | A | 1 | a0001c0001t0068g0096 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.2312+11185G>T | FAM120C | ENSG00000184083.12 | transcript | ENST00000375180.7 | protein_coding | 10/15 | chrX | 54105360 | ||||||
chrX:54105956
|
T | A | 3 | a0001c0001t0018g0115a0001c0001t0018g0116a0001c0001t0018g0151 | 3 | HG02809.hp2 HG06807.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.2312+10589A>T | FAM120C | ENSG00000184083.12 | transcript | ENST00000375180.7 | protein_coding | 10/15 | chrX | 54105956 | ||||||
chrX:54106174
|
G | A | 3 | a0001c0001t0022g0119a0003c0003t0013g0121a0003c0003t0013g0122 | 3 | HG03098.hp1 HG03579.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.2312+10371C>T | FAM120C | ENSG00000184083.12 | transcript | ENST00000375180.7 | protein_coding | 10/15 | chrX | 54106174 | ||||||
chrX:54106244
|
C | A | 1 | a0001c0001t0011g0123 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.2312+10301G>T | FAM120C | ENSG00000184083.12 | transcript | ENST00000375180.7 | protein_coding | 10/15 | chrX | 54106244 | ||||||
chrX:54107102
|
G | GT | 2 | a0001c0001t0009g0070a0001c0001t0014g0094 | 2 | HG01109.hp1 HG02602.hp1 |
intron_variant | MODIFIER | c.2312+9442dupA | FAM120C | ENSG00000184083.12 | transcript | ENST00000375180.7 | protein_coding | 10/15 | chrX | 54107102 | ||||||
chrX:54107102
|
GT | G | 1 | a0001c0001t0006g0053 | 1 | NA18988.hp1 | intron_variant | MODIFIER | c.2312+9442delA | FAM120C | ENSG00000184083.12 | transcript | ENST00000375180.7 | protein_coding | 10/15 | chrX | 54107102 | ||||||
chrX:54107276
|
T | C | 1 | a0001c0001t0029g0088 | 1 | HG03492.hp1 | intron_variant | MODIFIER | c.2312+9269A>G | FAM120C | ENSG00000184083.12 | transcript | ENST00000375180.7 | protein_coding | 10/15 | chrX | 54107276 | ||||||
chrX:54107527
|
A | T | 6 | a0001c0001t0018g0115a0001c0001t0018g0116a0001c0001t0018g0151others(3): Show | 6 | HG02572.hp1 HG02615.hp2 HG02809.hp2 others(3): Show |
intron_variant | MODIFIER | c.2312+9018T>A | FAM120C | ENSG00000184083.12 | transcript | ENST00000375180.7 | protein_coding | 10/15 | chrX | 54107527 | ||||||
chrX:54107528
|
T | A | 1 | a0001c0001t0031g0138 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.2312+9017A>T | FAM120C | ENSG00000184083.12 | transcript | ENST00000375180.7 | protein_coding | 10/15 | chrX | 54107528 | ||||||
chrX:54107612
|
C | T | 1 | a0001c0001t0024g0080 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.2312+8933G>A | FAM120C | ENSG00000184083.12 | transcript | ENST00000375180.7 | protein_coding | 10/15 | chrX | 54107612 | ||||||
chrX:54107615
|
G | A | 3 | a0001c0001t0033g0012a0001c0001t0033g0013a0001c0001t0072g0106 | 3 | HG02559.hp2 HG02647.hp1 HG02809.hp1 |
intron_variant | MODIFIER | c.2312+8930C>T | FAM120C | ENSG00000184083.12 | transcript | ENST00000375180.7 | protein_coding | 10/15 | chrX | 54107615 | ||||||
chrX:54107935
|
C | A | 9 | a0001c0001t0018g0115a0001c0001t0018g0116a0001c0001t0018g0151others(6): Show | 9 | HG02559.hp2 HG02572.hp1 HG02615.hp2 others(6): Show |
intron_variant | MODIFIER | c.2312+8610G>T | FAM120C | ENSG00000184083.12 | transcript | ENST00000375180.7 | protein_coding | 10/15 | chrX | 54107935 | ||||||
chrX:54108084
|
T | A | 25 | a0001c0001t0001g0177a0001c0001t0002g0159a0001c0001t0002g0160others(22): Show | 26 | HG00558.hp2 HG00609.hp1 HG00621.hp1 others(23): Show |
intron_variant | MODIFIER | c.2312+8461A>T | FAM120C | ENSG00000184083.12 | transcript | ENST00000375180.7 | protein_coding | 10/15 | chrX | 54108084 | ||||||
chrX:54108127
|
CA | C | 22 | a0001c0001t0013g0112a0001c0001t0015g0015a0001c0001t0015g0097others(19): Show | 22 | HG00735.hp1 HG00738.hp1 HG01243.hp1 others(19): Show |
intron_variant | MODIFIER | c.2312+8417delT | FAM120C | ENSG00000184083.12 | transcript | ENST00000375180.7 | protein_coding | 10/15 | chrX | 54108127 | ||||||
chrX:54108488
|
CA | C | 1 | a0001c0001t0005g0062 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.2312+8056delT | FAM120C | ENSG00000184083.12 | transcript | ENST00000375180.7 | protein_coding | 10/15 | chrX | 54108488 | ||||||
chrX:54108584
|
T | TG | 1 | a0005c0007t0034g0007 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.2312+7960dupC | FAM120C | ENSG00000184083.12 | transcript | ENST00000375180.7 | protein_coding | 10/15 | chrX | 54108584 | ||||||
chrX:54108606
|
T | C | 1 | a0001c0001t0050g0051 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.2312+7939A>G | FAM120C | ENSG00000184083.12 | transcript | ENST00000375180.7 | protein_coding | 10/15 | chrX | 54108606 | ||||||
chrX:54108696
|
C | A | 180 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0022others(177): Show | 182 | HG00140.hp1 HG00280.hp1 HG00558.hp1 others(179): Show |
intron_variant | MODIFIER | c.2312+7849G>T | FAM120C | ENSG00000184083.12 | transcript | ENST00000375180.7 | protein_coding | 10/15 | chrX | 54108696 | ||||||
chrX:54108930
|
C | CA | 2 | a0001c0001t0008g0158a0001c0001t0023g0109 | 2 | HG00621.hp1 HG02027.hp1 |
intron_variant | MODIFIER | c.2312+7614dupT | FAM120C | ENSG00000184083.12 | transcript | ENST00000375180.7 | protein_coding | 10/15 | chrX | 54108930 | ||||||
chrX:54108930
|
C | CAA | 1 | a0001c0001t0052g0100 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.2312+7613_2312+761 others(6): Show |
FAM120C | ENSG00000184083.12 | transcript | ENST00000375180.7 | protein_coding | 10/15 | chrX | 54108930 | ||||||
chrX:54109006
|
A | C | 2 | a0001c0001t0058g0020a0001c0001t0061g0019 | 2 | HG01069.hp1 HG01952.hp1 |
intron_variant | MODIFIER | c.2312+7539T>G | FAM120C | ENSG00000184083.12 | transcript | ENST00000375180.7 | protein_coding | 10/15 | chrX | 54109006 | ||||||
chrX:54109286
|
TA | T | 1 | a0005c0007t0034g0007 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.2312+7258delT | FAM120C | ENSG00000184083.12 | transcript | ENST00000375180.7 | protein_coding | 10/15 | chrX | 54109286 | ||||||
chrX:54109416
|
T | C | 187 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0022others(184): Show | 189 | HG00140.hp1 HG00280.hp1 HG00558.hp1 others(186): Show |
intron_variant | MODIFIER | c.2312+7129A>G | FAM120C | ENSG00000184083.12 | transcript | ENST00000375180.7 | protein_coding | 10/15 | chrX | 54109416 | ||||||
chrX:54109593
|
T | C | 1 | a0001c0001t0014g0075 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.2312+6952A>G | FAM120C | ENSG00000184083.12 | transcript | ENST00000375180.7 | protein_coding | 10/15 | chrX | 54109593 | ||||||
chrX:54109594
|
G | A | 1 | a0001c0001t0001g0042 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.2312+6951C>T | FAM120C | ENSG00000184083.12 | transcript | ENST00000375180.7 | protein_coding | 10/15 | chrX | 54109594 | ||||||
chrX:54109615
|
T | TA | 2 | a0001c0001t0067g0018a0001c0005t0006g0004 | 2 | HG02257.hp1 NA18959.hp1 |
intron_variant | MODIFIER | c.2312+6929dupT | FAM120C | ENSG00000184083.12 | transcript | ENST00000375180.7 | protein_coding | 10/15 | chrX | 54109615 | ||||||
chrX:54109615
|
TA | T | 2 | a0001c0001t0010g0072a0001c0001t0028g0066 | 2 | NA18969.hp1 NA20805.hp1 |
intron_variant | MODIFIER | c.2312+6929delT | FAM120C | ENSG00000184083.12 | transcript | ENST00000375180.7 | protein_coding | 10/15 | chrX | 54109615 | ||||||
chrX:54109761
|
G | A | 1 | a0001c0001t0019g0120 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.2312+6784C>T | FAM120C | ENSG00000184083.12 | transcript | ENST00000375180.7 | protein_coding | 10/15 | chrX | 54109761 | ||||||
chrX:54109815
|
T | TA | 1 | a0001c0001t0005g0062 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.2312+6729dupT | FAM120C | ENSG00000184083.12 | transcript | ENST00000375180.7 | protein_coding | 10/15 | chrX | 54109815 | ||||||
chrX:54109826
|
A | C | 1 | a0001c0001t0044g0156 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.2312+6719T>G | FAM120C | ENSG00000184083.12 | transcript | ENST00000375180.7 | protein_coding | 10/15 | chrX | 54109826 | ||||||
chrX:54109935
|
T | C | 108 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0022others(105): Show | 109 | HG00140.hp1 HG00280.hp1 HG00558.hp1 others(106): Show |
intron_variant | MODIFIER | c.2312+6610A>G | FAM120C | ENSG00000184083.12 | transcript | ENST00000375180.7 | protein_coding | 10/15 | chrX | 54109935 | ||||||
chrX:54110011
|
C | CT | 142 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0022others(139): Show | 143 | HG00140.hp1 HG00280.hp1 HG00558.hp1 others(140): Show |
intron_variant | MODIFIER | c.2312+6533dupA | FAM120C | ENSG00000184083.12 | transcript | ENST00000375180.7 | protein_coding | 10/15 | chrX | 54110011 | ||||||
chrX:54110011
|
C | CTT | 8 | a0001c0001t0003g0110a0001c0001t0005g0062a0001c0001t0009g0033others(5): Show | 8 | HG01192.hp1 HG01433.hp1 HG02135.hp1 others(5): Show |
intron_variant | MODIFIER | c.2312+6532_2312+653 others(6): Show |
FAM120C | ENSG00000184083.12 | transcript | ENST00000375180.7 | protein_coding | 10/15 | chrX | 54110011 | ||||||
chrX:54110011
|
CT | C | 3 | a0001c0001t0033g0012a0001c0001t0033g0013a0001c0001t0072g0106 | 3 | HG02559.hp2 HG02647.hp1 HG02809.hp1 |
intron_variant | MODIFIER | c.2312+6533delA | FAM120C | ENSG00000184083.12 | transcript | ENST00000375180.7 | protein_coding | 10/15 | chrX | 54110011 | ||||||
chrX:54110011
|
CTT | C | 6 | a0001c0001t0018g0115a0001c0001t0018g0116a0001c0001t0018g0151others(3): Show | 6 | HG02572.hp1 HG02615.hp2 HG02809.hp2 others(3): Show |
intron_variant | MODIFIER | c.2312+6532_2312+653 others(6): Show |
FAM120C | ENSG00000184083.12 | transcript | ENST00000375180.7 | protein_coding | 10/15 | chrX | 54110011 | ||||||
chrX:54110297
|
T | C | 2 | a0001c0001t0043g0147a0001c0001t0045g0148 | 2 | HG02922.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.2312+6248A>G | FAM120C | ENSG00000184083.12 | transcript | ENST00000375180.7 | protein_coding | 10/15 | chrX | 54110297 | ||||||
chrX:54110330
|
AAAT | A | 3 | a0001c0001t0001g0036a0001c0001t0001g0052a0001c0001t0023g0109 | 3 | HG02027.hp1 NA18940.hp1 NA18944.hp1 |
intron_variant | MODIFIER | c.2312+6212_2312+621 others(7): Show |
FAM120C | ENSG00000184083.12 | transcript | ENST00000375180.7 | protein_coding | 10/15 | chrX | 54110330 | ||||||
chrX:54110539
|
AGGT | A | 3 | a0001c0001t0033g0012a0001c0001t0033g0013a0001c0001t0072g0106 | 3 | HG02559.hp2 HG02647.hp1 HG02809.hp1 |
intron_variant | MODIFIER | c.2312+6003_2312+600 others(7): Show |
FAM120C | ENSG00000184083.12 | transcript | ENST00000375180.7 | protein_coding | 10/15 | chrX | 54110539 | ||||||
chrX:54110590
|
T | C | 3 | a0001c0001t0033g0012a0001c0001t0033g0013a0001c0001t0072g0106 | 3 | HG02559.hp2 HG02647.hp1 HG02809.hp1 |
intron_variant | MODIFIER | c.2312+5955A>G | FAM120C | ENSG00000184083.12 | transcript | ENST00000375180.7 | protein_coding | 10/15 | chrX | 54110590 | ||||||
chrX:54110831
|
G | A | 10 | a0001c0001t0016g0137a0001c0001t0016g0139a0001c0001t0016g0141others(7): Show | 10 | HG01255.hp1 HG01884.hp2 HG02055.hp1 others(7): Show |
intron_variant | MODIFIER | c.2312+5714C>T | FAM120C | ENSG00000184083.12 | transcript | ENST00000375180.7 | protein_coding | 10/15 | chrX | 54110831 | ||||||
chrX:54111059
|
CA | C | 3 | a0001c0001t0002g0159a0001c0001t0003g0032a0001c0001t0028g0066 | 3 | HG02040.hp1 NA18986.hp1 NA20805.hp1 |
intron_variant | MODIFIER | c.2312+5485delT | FAM120C | ENSG00000184083.12 | transcript | ENST00000375180.7 | protein_coding | 10/15 | chrX | 54111059 | ||||||
chrX:54111544
|
CA | C | 172 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0022others(169): Show | 174 | HG00140.hp1 HG00280.hp1 HG00558.hp1 others(171): Show |
intron_variant | MODIFIER | c.2312+5000delT | FAM120C | ENSG00000184083.12 | transcript | ENST00000375180.7 | protein_coding | 10/15 | chrX | 54111544 | ||||||
chrX:54111824
|
C | CCAAAACA others(8): Show |
1 | a0001c0001t0001g0177 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.2312+4706_2312+472 others(19): Show |
FAM120C | ENSG00000184083.12 | transcript | ENST00000375180.7 | protein_coding | 10/15 | chrX | 54111824 | ||||||
chrX:54112273
|
G | A | 1 | a0001c0001t0052g0100 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.2312+4272C>T | FAM120C | ENSG00000184083.12 | transcript | ENST00000375180.7 | protein_coding | 10/15 | chrX | 54112273 | ||||||
chrX:54112840
|
CA | C | 7 | a0001c0001t0009g0033a0001c0001t0009g0034a0001c0001t0009g0070others(4): Show | 7 | HG01109.hp1 HG02056.hp1 HG02074.hp1 others(4): Show |
intron_variant | MODIFIER | c.2312+3704delT | FAM120C | ENSG00000184083.12 | transcript | ENST00000375180.7 | protein_coding | 10/15 | chrX | 54112840 | ||||||
chrX:54112840
|
CAA | C | 169 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0022others(166): Show | 171 | HG00140.hp1 HG00280.hp1 HG00558.hp1 others(168): Show |
intron_variant | MODIFIER | c.2312+3703_2312+370 others(6): Show |
FAM120C | ENSG00000184083.12 | transcript | ENST00000375180.7 | protein_coding | 10/15 | chrX | 54112840 | ||||||
chrX:54112840
|
CAAA | C | 1 | a0001c0001t0002g0159 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.2312+3702_2312+370 others(7): Show |
FAM120C | ENSG00000184083.12 | transcript | ENST00000375180.7 | protein_coding | 10/15 | chrX | 54112840 | ||||||
chrX:54113015
|
C | T | 36 | a0001c0001t0001g0177a0001c0001t0002g0132a0001c0001t0002g0159others(33): Show | 37 | HG00558.hp2 HG00609.hp1 HG00621.hp1 others(34): Show |
intron_variant | MODIFIER | c.2312+3530G>A | FAM120C | ENSG00000184083.12 | transcript | ENST00000375180.7 | protein_coding | 10/15 | chrX | 54113015 | ||||||
chrX:54113329
|
G | A | 6 | a0001c0001t0018g0115a0001c0001t0018g0116a0001c0001t0018g0151others(3): Show | 6 | HG02572.hp1 HG02615.hp2 HG02809.hp2 others(3): Show |
intron_variant | MODIFIER | c.2312+3216C>T | FAM120C | ENSG00000184083.12 | transcript | ENST00000375180.7 | protein_coding | 10/15 | chrX | 54113329 | ||||||
chrX:54113459
|
C | CA | 1 | a0001c0001t0009g0049 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.2312+3085dupT | FAM120C | ENSG00000184083.12 | transcript | ENST00000375180.7 | protein_coding | 10/15 | chrX | 54113459 | ||||||
chrX:54113507
|
AG | A | 1 | a0001c0001t0058g0020 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.2312+3037delC | FAM120C | ENSG00000184083.12 | transcript | ENST00000375180.7 | protein_coding | 10/15 | chrX | 54113507 | ||||||
chrX:54113639
|
C | T | 1 | a0001c0001t0005g0095 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.2312+2906G>A | FAM120C | ENSG00000184083.12 | transcript | ENST00000375180.7 | protein_coding | 10/15 | chrX | 54113639 | ||||||
chrX:54113682
|
TG | T | 1 | a0001c0001t0058g0020 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.2312+2862delC | FAM120C | ENSG00000184083.12 | transcript | ENST00000375180.7 | protein_coding | 10/15 | chrX | 54113682 | ||||||
chrX:54113689
|
A | T | 1 | a0001c0001t0042g0183 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.2312+2856T>A | FAM120C | ENSG00000184083.12 | transcript | ENST00000375180.7 | protein_coding | 10/15 | chrX | 54113689 | ||||||
chrX:54113747
|
GA | G | 2 | a0001c0001t0055g0048a0001c0001t0058g0020 | 2 | HG01069.hp1 HG02071.hp1 |
intron_variant | MODIFIER | c.2312+2797delT | FAM120C | ENSG00000184083.12 | transcript | ENST00000375180.7 | protein_coding | 10/15 | chrX | 54113747 | ||||||
chrX:54113759
|
A | T | 5 | a0001c0001t0002g0132a0001c0001t0008g0124a0001c0001t0008g0125others(2): Show | 5 | HG01081.hp1 HG02258.hp1 HG02451.hp1 others(2): Show |
intron_variant | MODIFIER | c.2312+2786T>A | FAM120C | ENSG00000184083.12 | transcript | ENST00000375180.7 | protein_coding | 10/15 | chrX | 54113759 | ||||||
chrX:54113939
|
A | AT | 1 | a0001c0001t0005g0037 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.2312+2605_2312+260 others(5): Show |
FAM120C | ENSG00000184083.12 | transcript | ENST00000375180.7 | protein_coding | 10/15 | chrX | 54113939 | ||||||
chrX:54113969
|
A | G | 1 | a0001c0001t0038g0090 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.2312+2576T>C | FAM120C | ENSG00000184083.12 | transcript | ENST00000375180.7 | protein_coding | 10/15 | chrX | 54113969 | ||||||
chrX:54114039
|
T | TAC | 4 | a0002c0002t0001g0187a0002c0002t0007g0184a0002c0002t0019g0186others(1): Show | 4 | HG00280.hp1 HG00642.hp1 HG00735.hp2 others(1): Show |
intron_variant | MODIFIER | c.2312+2504_2312+250 others(6): Show |
FAM120C | ENSG00000184083.12 | transcript | ENST00000375180.7 | protein_coding | 10/15 | chrX | 54114039 | ||||||
chrX:54114039
|
TAC | T | 141 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0022others(138): Show | 143 | HG00140.hp1 HG00558.hp1 HG00609.hp1 others(140): Show |
intron_variant | MODIFIER | c.2312+2504_2312+250 others(6): Show |
FAM120C | ENSG00000184083.12 | transcript | ENST00000375180.7 | protein_coding | 10/15 | chrX | 54114039 | ||||||
chrX:54114039
|
TACAC | T | 27 | a0001c0001t0002g0132a0001c0001t0002g0174a0001c0001t0008g0124others(24): Show | 27 | HG00558.hp2 HG00735.hp1 HG01081.hp1 others(24): Show |
intron_variant | MODIFIER | c.2312+2502_2312+250 others(8): Show |
FAM120C | ENSG00000184083.12 | transcript | ENST00000375180.7 | protein_coding | 10/15 | chrX | 54114039 | ||||||
chrX:54114039
|
TACACACA others(5): Show |
T | 5 | a0001c0001t0002g0172a0001c0001t0004g0045a0001c0001t0011g0163others(2): Show | 5 | HG01070.hp1 HG01074.hp1 HG01257.hp2 others(2): Show |
intron_variant | MODIFIER | c.2312+2494_2312+250 others(16): Show |
FAM120C | ENSG00000184083.12 | transcript | ENST00000375180.7 | protein_coding | 10/15 | chrX | 54114039 | ||||||
chrX:54114418
|
G | GT | 1 | a0001c0001t0058g0020 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.2312+2126dupA | FAM120C | ENSG00000184083.12 | transcript | ENST00000375180.7 | protein_coding | 10/15 | chrX | 54114418 | ||||||
chrX:54114419
|
T | G | 3 | a0001c0001t0033g0012a0001c0001t0033g0013a0001c0001t0072g0106 | 3 | HG02559.hp2 HG02647.hp1 HG02809.hp1 |
intron_variant | MODIFIER | c.2312+2126A>C | FAM120C | ENSG00000184083.12 | transcript | ENST00000375180.7 | protein_coding | 10/15 | chrX | 54114419 | ||||||
chrX:54114434
|
G | GT | 1 | a0001c0001t0003g0041 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.2312+2110dupA | FAM120C | ENSG00000184083.12 | transcript | ENST00000375180.7 | protein_coding | 10/15 | chrX | 54114434 | ||||||
chrX:54114443
|
G | GT | 5 | a0001c0001t0004g0071a0001c0001t0032g0178a0001c0001t0037g0129others(2): Show | 5 | HG01069.hp1 HG01261.hp1 HG02074.hp1 others(2): Show |
intron_variant | MODIFIER | c.2312+2101dupA | FAM120C | ENSG00000184083.12 | transcript | ENST00000375180.7 | protein_coding | 10/15 | chrX | 54114443 | ||||||
chrX:54114443
|
GT | G | 2 | a0001c0001t0001g0060a0001c0001t0001g0061 | 2 | NA19009.hp1 NA19066.hp1 |
intron_variant | MODIFIER | c.2312+2101delA | FAM120C | ENSG00000184083.12 | transcript | ENST00000375180.7 | protein_coding | 10/15 | chrX | 54114443 | ||||||
chrX:54114444
|
T | G | 1 | a0001c0001t0041g0098 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.2312+2101A>C | FAM120C | ENSG00000184083.12 | transcript | ENST00000375180.7 | protein_coding | 10/15 | chrX | 54114444 | ||||||
chrX:54114536
|
CG | C | 1 | a0001c0001t0058g0020 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.2312+2008delC | FAM120C | ENSG00000184083.12 | transcript | ENST00000375180.7 | protein_coding | 10/15 | chrX | 54114536 | ||||||
chrX:54114554
|
C | T | 1 | a0001c0001t0001g0027 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.2312+1991G>A | FAM120C | ENSG00000184083.12 | transcript | ENST00000375180.7 | protein_coding | 10/15 | chrX | 54114554 | ||||||
chrX:54114728
|
T | C | 2 | a0001c0001t0027g0117a0001c0001t0027g0118 | 2 | HG06807.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.2312+1817A>G | FAM120C | ENSG00000184083.12 | transcript | ENST00000375180.7 | protein_coding | 10/15 | chrX | 54114728 | ||||||
chrX:54114810
|
C | A | 1 | a0001c0001t0025g0146 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.2312+1735G>T | FAM120C | ENSG00000184083.12 | transcript | ENST00000375180.7 | protein_coding | 10/15 | chrX | 54114810 | ||||||
chrX:54114922
|
A | AT | 1 | a0001c0001t0032g0108 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.2312+1622dupA | FAM120C | ENSG00000184083.12 | transcript | ENST00000375180.7 | protein_coding | 10/15 | chrX | 54114922 | ||||||
chrX:54115351
|
T | C | 2 | a0001c0001t0027g0117a0001c0001t0027g0118 | 2 | HG06807.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.2312+1194A>G | FAM120C | ENSG00000184083.12 | transcript | ENST00000375180.7 | protein_coding | 10/15 | chrX | 54115351 | ||||||
chrX:54115367
|
T | G | 2 | a0002c0002t0019g0186a0002c0002t0047g0185 | 2 | HG00642.hp1 HG00735.hp2 |
intron_variant | MODIFIER | c.2312+1178A>C | FAM120C | ENSG00000184083.12 | transcript | ENST00000375180.7 | protein_coding | 10/15 | chrX | 54115367 | ||||||
chrX:54115415
|
A | G | 1 | a0001c0001t0009g0034 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.2312+1130T>C | FAM120C | ENSG00000184083.12 | transcript | ENST00000375180.7 | protein_coding | 10/15 | chrX | 54115415 | ||||||
chrX:54115538
|
T | G | 2 | a0001c0001t0004g0180a0001c0001t0009g0070 | 2 | HG01081.hp2 HG01109.hp1 |
intron_variant | MODIFIER | c.2312+1007A>C | FAM120C | ENSG00000184083.12 | transcript | ENST00000375180.7 | protein_coding | 10/15 | chrX | 54115538 | ||||||
chrX:54115554
|
T | C | 1 | a0001c0001t0031g0145 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.2312+991A>G | FAM120C | ENSG00000184083.12 | transcript | ENST00000375180.7 | protein_coding | 10/15 | chrX | 54115554 | ||||||
chrX:54115572
|
G | A | 2 | a0001c0001t0033g0012a0001c0001t0033g0013 | 2 | HG02559.hp2 HG02647.hp1 |
intron_variant | MODIFIER | c.2312+973C>T | FAM120C | ENSG00000184083.12 | transcript | ENST00000375180.7 | protein_coding | 10/15 | chrX | 54115572 | ||||||
chrX:54116386
|
G | A | 1 | a0001c0001t0067g0018 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.2312+159C>T | FAM120C | ENSG00000184083.12 | transcript | ENST00000375180.7 | protein_coding | 10/15 | chrX | 54116386 | ||||||
chrX:54116442
|
T | TA | 1 | a0003c0003t0013g0122 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.2312+102dupT | FAM120C | ENSG00000184083.12 | transcript | ENST00000375180.7 | protein_coding | 10/15 | chrX | 54116442 | ||||||
chrX:54116892
|
T | C | 5 | a0001c0001t0002g0132a0001c0001t0008g0124a0001c0001t0008g0125others(2): Show | 5 | HG01081.hp1 HG02258.hp1 HG02451.hp1 others(2): Show |
intron_variant | MODIFIER | c.2063-98A>G | FAM120C | ENSG00000184083.12 | transcript | ENST00000375180.7 | protein_coding | 9/15 | chrX | 54116892 | ||||||
chrX:54117028
|
T | C | 3 | a0001c0001t0033g0012a0001c0001t0033g0013a0001c0001t0072g0106 | 3 | HG02559.hp2 HG02647.hp1 HG02809.hp1 |
intron_variant | MODIFIER | c.2063-234A>G | FAM120C | ENSG00000184083.12 | transcript | ENST00000375180.7 | protein_coding | 9/15 | chrX | 54117028 | ||||||
chrX:54117098
|
C | T | 6 | a0001c0001t0018g0115a0001c0001t0018g0116a0001c0001t0018g0151others(3): Show | 6 | HG02572.hp1 HG02615.hp2 HG02809.hp2 others(3): Show |
intron_variant | MODIFIER | c.2063-304G>A | FAM120C | ENSG00000184083.12 | transcript | ENST00000375180.7 | protein_coding | 9/15 | chrX | 54117098 | ||||||
chrX:54117232
|
G | A | 1 | a0001c0001t0019g0120 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.2063-438C>T | FAM120C | ENSG00000184083.12 | transcript | ENST00000375180.7 | protein_coding | 9/15 | chrX | 54117232 | ||||||
chrX:54117352
|
C | CTAACACT others(190): Show |
1 | a0001c0001t0013g0130 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.2063-559_2063-558i others(199): Show |
FAM120C | ENSG00000184083.12 | transcript | ENST00000375180.7 | protein_coding | 9/15 | chrX | 54117352 | ||||||
chrX:54117354
|
A | AAAAAT | 7 | a0001c0001t0015g0133a0001c0001t0015g0136a0001c0001t0022g0149others(4): Show | 7 | HG02630.hp2 HG02647.hp1 HG02895.hp1 others(4): Show |
intron_variant | MODIFIER | c.2063-565_2063-561d others(7): Show |
FAM120C | ENSG00000184083.12 | transcript | ENST00000375180.7 | protein_coding | 9/15 | chrX | 54117354 | ||||||
chrX:54117354
|
A | AAAAATAA others(3): Show |
11 | a0001c0001t0008g0124a0001c0001t0008g0125a0001c0001t0011g0123others(8): Show | 11 | HG02258.hp1 HG02451.hp1 HG02559.hp1 others(8): Show |
intron_variant | MODIFIER | c.2063-570_2063-561d others(12): Show |
FAM120C | ENSG00000184083.12 | transcript | ENST00000375180.7 | protein_coding | 9/15 | chrX | 54117354 | ||||||
chrX:54117354
|
A | AAAAATAA others(8): Show |
6 | a0001c0001t0002g0132a0001c0001t0017g0154a0001c0001t0043g0147others(3): Show | 6 | HG01081.hp1 HG01257.hp2 HG02572.hp1 others(3): Show |
intron_variant | MODIFIER | c.2063-575_2063-561d others(17): Show |
FAM120C | ENSG00000184083.12 | transcript | ENST00000375180.7 | protein_coding | 9/15 | chrX | 54117354 | ||||||
chrX:54117354
|
A | AAAAATAA others(13): Show |
3 | a0001c0001t0002g0161a0001c0001t0044g0156a0001c0001t0045g0148 | 3 | HG02015.hp1 HG02698.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.2063-580_2063-561d others(22): Show |
FAM120C | ENSG00000184083.12 | transcript | ENST00000375180.7 | protein_coding | 9/15 | chrX | 54117354 | ||||||
chrX:54117354
|
A | AAAAATAA others(18): Show |
15 | a0001c0001t0002g0153a0001c0001t0002g0159a0001c0001t0002g0160others(12): Show | 16 | HG00609.hp1 HG01070.hp1 HG01074.hp1 others(13): Show |
intron_variant | MODIFIER | c.2063-585_2063-561d others(27): Show |
FAM120C | ENSG00000184083.12 | transcript | ENST00000375180.7 | protein_coding | 9/15 | chrX | 54117354 | ||||||
chrX:54117354
|
A | AAAAATAA others(23): Show |
3 | a0001c0001t0008g0158a0001c0001t0017g0005a0001c0001t0017g0171 | 3 | HG00621.hp1 HG01167.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.2063-590_2063-561d others(32): Show |
FAM120C | ENSG00000184083.12 | transcript | ENST00000375180.7 | protein_coding | 9/15 | chrX | 54117354 | ||||||
chrX:54117354
|
A | AAAAATAA others(28): Show |
1 | a0001c0001t0011g0155 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.2063-595_2063-561d others(37): Show |
FAM120C | ENSG00000184083.12 | transcript | ENST00000375180.7 | protein_coding | 9/15 | chrX | 54117354 | ||||||
chrX:54117354
|
A | AAAAATAA others(33): Show |
2 | a0001c0001t0010g0175a0001c0001t0017g0176 | 2 | HG02257.hp2 NA18980.hp2 |
intron_variant | MODIFIER | c.2063-600_2063-561d others(42): Show |
FAM120C | ENSG00000184083.12 | transcript | ENST00000375180.7 | protein_coding | 9/15 | chrX | 54117354 | ||||||
chrX:54117354
|
A | AAAAATAA others(828): Show |
1 | a0001c0001t0032g0178 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.2063-561_2063-560i others(837): Show |
FAM120C | ENSG00000184083.12 | transcript | ENST00000375180.7 | protein_coding | 9/15 | chrX | 54117354 | ||||||
chrX:54117354
|
A | AAAACTAA others(748): Show |
1 | a0001c0001t0002g0174 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.2063-561_2063-560i others(757): Show |
FAM120C | ENSG00000184083.12 | transcript | ENST00000375180.7 | protein_coding | 9/15 | chrX | 54117354 | ||||||
chrX:54117354
|
A | AAAACTAA others(283): Show |
1 | a0001c0001t0001g0177 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.2063-561_2063-560i others(292): Show |
FAM120C | ENSG00000184083.12 | transcript | ENST00000375180.7 | protein_coding | 9/15 | chrX | 54117354 | ||||||
chrX:54117354
|
AAAAAT | A | 104 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0022others(101): Show | 105 | HG00140.hp1 HG00280.hp1 HG00558.hp1 others(102): Show |
intron_variant | MODIFIER | c.2063-565_2063-561d others(7): Show |
FAM120C | ENSG00000184083.12 | transcript | ENST00000375180.7 | protein_coding | 9/15 | chrX | 54117354 | ||||||
chrX:54117354
|
AAAAATAA others(3): Show |
A | 3 | a0001c0001t0023g0109a0001c0001t0056g0103a0001c0001t0069g0074 | 3 | HG02027.hp1 HG03209.hp1 NA20905.hp1 |
intron_variant | MODIFIER | c.2063-570_2063-561d others(12): Show |
FAM120C | ENSG00000184083.12 | transcript | ENST00000375180.7 | protein_coding | 9/15 | chrX | 54117354 | ||||||
chrX:54117354
|
AAAAATAA others(8): Show |
A | 3 | a0001c0001t0013g0112a0001c0001t0028g0066a0001c0001t0031g0145 | 3 | HG01255.hp1 HG02630.hp1 NA20805.hp1 |
intron_variant | MODIFIER | c.2063-575_2063-561d others(17): Show |
FAM120C | ENSG00000184083.12 | transcript | ENST00000375180.7 | protein_coding | 9/15 | chrX | 54117354 | ||||||
chrX:54117354
|
AAAAATAA others(13): Show |
A | 1 | a0001c0001t0012g0035 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.2063-580_2063-561d others(22): Show |
FAM120C | ENSG00000184083.12 | transcript | ENST00000375180.7 | protein_coding | 9/15 | chrX | 54117354 | ||||||
chrX:54117357
|
A | AATAACAT others(128): Show |
1 | a0001c0001t0057g0173 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.2063-564_2063-563i others(137): Show |
FAM120C | ENSG00000184083.12 | transcript | ENST00000375180.7 | protein_coding | 9/15 | chrX | 54117357 | ||||||
chrX:54117358
|
A | C | 2 | a0001c0001t0001g0177a0001c0001t0002g0174 | 2 | HG00558.hp2 NA18973.hp2 |
intron_variant | MODIFIER | c.2063-564T>G | FAM120C | ENSG00000184083.12 | transcript | ENST00000375180.7 | protein_coding | 9/15 | chrX | 54117358 | ||||||
chrX:54117358
|
A | T | 1 | a0001c0001t0013g0130 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.2063-564T>A | FAM120C | ENSG00000184083.12 | transcript | ENST00000375180.7 | protein_coding | 9/15 | chrX | 54117358 | ||||||
chrX:54117362
|
A | C | 1 | a0001c0001t0057g0173 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.2063-568T>G | FAM120C | ENSG00000184083.12 | transcript | ENST00000375180.7 | protein_coding | 9/15 | chrX | 54117362 | ||||||
chrX:54117363
|
A | C | 2 | a0001c0001t0001g0177a0001c0001t0002g0174 | 2 | HG00558.hp2 NA18973.hp2 |
intron_variant | MODIFIER | c.2063-569T>G | FAM120C | ENSG00000184083.12 | transcript | ENST00000375180.7 | protein_coding | 9/15 | chrX | 54117363 | ||||||
chrX:54117367
|
A | C | 1 | a0001c0001t0057g0173 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.2063-573T>G | FAM120C | ENSG00000184083.12 | transcript | ENST00000375180.7 | protein_coding | 9/15 | chrX | 54117367 | ||||||
chrX:54117368
|
A | C | 2 | a0001c0001t0001g0177a0001c0001t0002g0174 | 2 | HG00558.hp2 NA18973.hp2 |
intron_variant | MODIFIER | c.2063-574T>G | FAM120C | ENSG00000184083.12 | transcript | ENST00000375180.7 | protein_coding | 9/15 | chrX | 54117368 | ||||||
chrX:54117372
|
A | C | 1 | a0001c0001t0057g0173 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.2063-578T>G | FAM120C | ENSG00000184083.12 | transcript | ENST00000375180.7 | protein_coding | 9/15 | chrX | 54117372 | ||||||
chrX:54117373
|
A | C | 2 | a0001c0001t0001g0177a0001c0001t0002g0174 | 2 | HG00558.hp2 NA18973.hp2 |
intron_variant | MODIFIER | c.2063-579T>G | FAM120C | ENSG00000184083.12 | transcript | ENST00000375180.7 | protein_coding | 9/15 | chrX | 54117373 | ||||||
chrX:54117377
|
A | C | 1 | a0001c0001t0057g0173 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.2063-583T>G | FAM120C | ENSG00000184083.12 | transcript | ENST00000375180.7 | protein_coding | 9/15 | chrX | 54117377 | ||||||
chrX:54117378
|
A | C | 2 | a0001c0001t0001g0177a0001c0001t0002g0174 | 2 | HG00558.hp2 NA18973.hp2 |
intron_variant | MODIFIER | c.2063-584T>G | FAM120C | ENSG00000184083.12 | transcript | ENST00000375180.7 | protein_coding | 9/15 | chrX | 54117378 | ||||||
chrX:54117382
|
A | C | 1 | a0001c0001t0057g0173 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.2063-588T>G | FAM120C | ENSG00000184083.12 | transcript | ENST00000375180.7 | protein_coding | 9/15 | chrX | 54117382 | ||||||
chrX:54117383
|
A | C | 2 | a0001c0001t0001g0177a0001c0001t0002g0174 | 2 | HG00558.hp2 NA18973.hp2 |
intron_variant | MODIFIER | c.2063-589T>G | FAM120C | ENSG00000184083.12 | transcript | ENST00000375180.7 | protein_coding | 9/15 | chrX | 54117383 | ||||||
chrX:54117387
|
A | C | 1 | a0001c0001t0057g0173 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.2063-593T>G | FAM120C | ENSG00000184083.12 | transcript | ENST00000375180.7 | protein_coding | 9/15 | chrX | 54117387 | ||||||
chrX:54117388
|
A | C | 2 | a0001c0001t0001g0177a0001c0001t0002g0174 | 2 | HG00558.hp2 NA18973.hp2 |
intron_variant | MODIFIER | c.2063-594T>G | FAM120C | ENSG00000184083.12 | transcript | ENST00000375180.7 | protein_coding | 9/15 | chrX | 54117388 | ||||||
chrX:54117392
|
A | C | 1 | a0001c0001t0057g0173 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.2063-598T>G | FAM120C | ENSG00000184083.12 | transcript | ENST00000375180.7 | protein_coding | 9/15 | chrX | 54117392 | ||||||
chrX:54117393
|
A | C | 2 | a0001c0001t0001g0177a0001c0001t0002g0174 | 2 | HG00558.hp2 NA18973.hp2 |
intron_variant | MODIFIER | c.2063-599T>G | FAM120C | ENSG00000184083.12 | transcript | ENST00000375180.7 | protein_coding | 9/15 | chrX | 54117393 | ||||||
chrX:54117397
|
A | C | 1 | a0001c0001t0057g0173 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.2063-603T>G | FAM120C | ENSG00000184083.12 | transcript | ENST00000375180.7 | protein_coding | 9/15 | chrX | 54117397 | ||||||
chrX:54117398
|
A | C | 2 | a0001c0001t0001g0177a0001c0001t0002g0174 | 2 | HG00558.hp2 NA18973.hp2 |
intron_variant | MODIFIER | c.2063-604T>G | FAM120C | ENSG00000184083.12 | transcript | ENST00000375180.7 | protein_coding | 9/15 | chrX | 54117398 | ||||||
chrX:54117402
|
A | C | 1 | a0001c0001t0057g0173 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.2063-608T>G | FAM120C | ENSG00000184083.12 | transcript | ENST00000375180.7 | protein_coding | 9/15 | chrX | 54117402 | ||||||
chrX:54117403
|
A | C | 2 | a0001c0001t0001g0177a0001c0001t0002g0174 | 2 | HG00558.hp2 NA18973.hp2 |
intron_variant | MODIFIER | c.2063-609T>G | FAM120C | ENSG00000184083.12 | transcript | ENST00000375180.7 | protein_coding | 9/15 | chrX | 54117403 | ||||||
chrX:54117407
|
A | C | 1 | a0001c0001t0057g0173 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.2063-613T>G | FAM120C | ENSG00000184083.12 | transcript | ENST00000375180.7 | protein_coding | 9/15 | chrX | 54117407 | ||||||
chrX:54117408
|
A | C | 2 | a0001c0001t0001g0177a0001c0001t0002g0174 | 2 | HG00558.hp2 NA18973.hp2 |
intron_variant | MODIFIER | c.2063-614T>G | FAM120C | ENSG00000184083.12 | transcript | ENST00000375180.7 | protein_coding | 9/15 | chrX | 54117408 | ||||||
chrX:54117413
|
A | C | 1 | a0001c0001t0002g0174 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.2063-619T>G | FAM120C | ENSG00000184083.12 | transcript | ENST00000375180.7 | protein_coding | 9/15 | chrX | 54117413 | ||||||
chrX:54117532
|
C | CA | 16 | a0001c0001t0001g0036a0001c0001t0001g0052a0001c0001t0001g0079others(13): Show | 16 | HG01069.hp1 HG01081.hp2 HG01192.hp1 others(13): Show |
intron_variant | MODIFIER | c.2063-739dupT | FAM120C | ENSG00000184083.12 | transcript | ENST00000375180.7 | protein_coding | 9/15 | chrX | 54117532 | ||||||
chrX:54117532
|
C | CAA | 1 | a0001c0001t0001g0044 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.2063-740_2063-739d others(4): Show |
FAM120C | ENSG00000184083.12 | transcript | ENST00000375180.7 | protein_coding | 9/15 | chrX | 54117532 | ||||||
chrX:54117629
|
C | T | 1 | a0001c0001t0005g0113 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.2063-835G>A | FAM120C | ENSG00000184083.12 | transcript | ENST00000375180.7 | protein_coding | 9/15 | chrX | 54117629 | ||||||
chrX:54117697
|
G | GA | 1 | a0001c0005t0006g0004 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.2063-904dupT | FAM120C | ENSG00000184083.12 | transcript | ENST00000375180.7 | protein_coding | 9/15 | chrX | 54117697 | ||||||
chrX:54117707
|
C | CA | 3 | a0001c0001t0007g0057a0001c0001t0008g0124a0001c0001t0026g0101 | 3 | HG02559.hp1 NA18943.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.2063-914dupT | FAM120C | ENSG00000184083.12 | transcript | ENST00000375180.7 | protein_coding | 9/15 | chrX | 54117707 | ||||||
chrX:54117759
|
C | A | 1 | a0001c0001t0002g0174 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.2063-965G>T | FAM120C | ENSG00000184083.12 | transcript | ENST00000375180.7 | protein_coding | 9/15 | chrX | 54117759 | ||||||
chrX:54117911
|
A | C | 1 | a0001c0001t0002g0172 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.2063-1117T>G | FAM120C | ENSG00000184083.12 | transcript | ENST00000375180.7 | protein_coding | 9/15 | chrX | 54117911 | ||||||
chrX:54118127
|
G | A | 2 | a0001c0001t0027g0117a0001c0001t0027g0118 | 2 | HG06807.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.2063-1333C>T | FAM120C | ENSG00000184083.12 | transcript | ENST00000375180.7 | protein_coding | 9/15 | chrX | 54118127 | ||||||
chrX:54118182
|
C | A | 1 | a0001c0001t0067g0018 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.2063-1388G>T | FAM120C | ENSG00000184083.12 | transcript | ENST00000375180.7 | protein_coding | 9/15 | chrX | 54118182 | ||||||
chrX:54118222
|
T | TA | 7 | a0001c0001t0001g0001a0001c0001t0004g0045a0001c0001t0008g0124others(4): Show | 8 | HG01070.hp1 HG01074.hp1 HG01257.hp1 others(5): Show |
intron_variant | MODIFIER | c.2063-1429dupT | FAM120C | ENSG00000184083.12 | transcript | ENST00000375180.7 | protein_coding | 9/15 | chrX | 54118222 | ||||||
chrX:54118222
|
TA | T | 1 | a0001c0001t0006g0026 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.2063-1429delT | FAM120C | ENSG00000184083.12 | transcript | ENST00000375180.7 | protein_coding | 9/15 | chrX | 54118222 | ||||||
chrX:54118320
|
T | C | 1 | a0001c0001t0060g0134 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.2063-1526A>G | FAM120C | ENSG00000184083.12 | transcript | ENST00000375180.7 | protein_coding | 9/15 | chrX | 54118320 | ||||||
chrX:54118326
|
A | G | 9 | a0001c0001t0018g0115a0001c0001t0018g0116a0001c0001t0018g0151others(6): Show | 9 | HG02559.hp2 HG02572.hp1 HG02615.hp2 others(6): Show |
intron_variant | MODIFIER | c.2063-1532T>C | FAM120C | ENSG00000184083.12 | transcript | ENST00000375180.7 | protein_coding | 9/15 | chrX | 54118326 | ||||||
chrX:54118369
|
T | C | 2 | a0001c0001t0002g0161a0001c0001t0002g0167 | 2 | HG02015.hp1 NA19007.hp1 |
intron_variant | MODIFIER | c.2063-1575A>G | FAM120C | ENSG00000184083.12 | transcript | ENST00000375180.7 | protein_coding | 9/15 | chrX | 54118369 | ||||||
chrX:54118591
|
T | C | 6 | a0001c0001t0018g0115a0001c0001t0018g0116a0001c0001t0018g0151others(3): Show | 6 | HG02572.hp1 HG02615.hp2 HG02809.hp2 others(3): Show |
intron_variant | MODIFIER | c.2063-1797A>G | FAM120C | ENSG00000184083.12 | transcript | ENST00000375180.7 | protein_coding | 9/15 | chrX | 54118591 | ||||||
chrX:54118651
|
T | C | 1 | a0001c0001t0004g0069 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.2063-1857A>G | FAM120C | ENSG00000184083.12 | transcript | ENST00000375180.7 | protein_coding | 9/15 | chrX | 54118651 | ||||||
chrX:54118699
|
C | CT | 4 | a0001c0001t0003g0040a0001c0001t0037g0129a0001c0001t0064g0082others(1): Show | 4 | HG02074.hp1 NA18959.hp1 NA18965.hp1 others(1): Show |
intron_variant | MODIFIER | c.2063-1906dupA | FAM120C | ENSG00000184083.12 | transcript | ENST00000375180.7 | protein_coding | 9/15 | chrX | 54118699 | ||||||
chrX:54118699
|
CT | C | 52 | a0001c0001t0001g0042a0001c0001t0001g0177a0001c0001t0002g0153others(49): Show | 53 | HG00558.hp2 HG00609.hp1 HG00621.hp1 others(50): Show |
intron_variant | MODIFIER | c.2063-1906delA | FAM120C | ENSG00000184083.12 | transcript | ENST00000375180.7 | protein_coding | 9/15 | chrX | 54118699 | ||||||
chrX:54118699
|
CTT | C | 11 | a0001c0001t0002g0132a0001c0001t0008g0162a0001c0001t0015g0136others(8): Show | 11 | HG01081.hp1 HG01169.hp1 HG01257.hp2 others(8): Show |
intron_variant | MODIFIER | c.2063-1907_2063-190 others(6): Show |
FAM120C | ENSG00000184083.12 | transcript | ENST00000375180.7 | protein_coding | 9/15 | chrX | 54118699 | ||||||
chrX:54118699
|
CTTT | C | 1 | a0001c0001t0003g0032 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.2063-1908_2063-190 others(7): Show |
FAM120C | ENSG00000184083.12 | transcript | ENST00000375180.7 | protein_coding | 9/15 | chrX | 54118699 | ||||||
chrX:54118707
|
T | C | 1 | a0001c0001t0072g0106 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.2063-1913A>G | FAM120C | ENSG00000184083.12 | transcript | ENST00000375180.7 | protein_coding | 9/15 | chrX | 54118707 | ||||||
chrX:54118709
|
T | C | 7 | a0001c0001t0018g0115a0001c0001t0018g0116a0001c0001t0018g0151others(4): Show | 7 | HG02572.hp1 HG02615.hp2 HG02809.hp2 others(4): Show |
intron_variant | MODIFIER | c.2063-1915A>G | FAM120C | ENSG00000184083.12 | transcript | ENST00000375180.7 | protein_coding | 9/15 | chrX | 54118709 | ||||||
chrX:54118725
|
TA | T | 1 | a0001c0001t0072g0106 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.2063-1932delT | FAM120C | ENSG00000184083.12 | transcript | ENST00000375180.7 | protein_coding | 9/15 | chrX | 54118725 | ||||||
chrX:54118726
|
A | T | 8 | a0001c0001t0018g0115a0001c0001t0018g0116a0001c0001t0018g0151others(5): Show | 8 | HG02559.hp2 HG02572.hp1 HG02615.hp2 others(5): Show |
intron_variant | MODIFIER | c.2063-1932T>A | FAM120C | ENSG00000184083.12 | transcript | ENST00000375180.7 | protein_coding | 9/15 | chrX | 54118726 | ||||||
chrX:54118780
|
T | C | 1 | a0001c0001t0073g0179 | 1 | NA19078.hp1 | intron_variant | MODIFIER | c.2063-1986A>G | FAM120C | ENSG00000184083.12 | transcript | ENST00000375180.7 | protein_coding | 9/15 | chrX | 54118780 | ||||||
chrX:54118858
|
T | TC | 1 | a0001c0001t0005g0095 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.2063-2065dupG | FAM120C | ENSG00000184083.12 | transcript | ENST00000375180.7 | protein_coding | 9/15 | chrX | 54118858 | ||||||
chrX:54118871
|
G | A | 3 | a0001c0001t0033g0012a0001c0001t0033g0013a0001c0001t0072g0106 | 3 | HG02559.hp2 HG02647.hp1 HG02809.hp1 |
intron_variant | MODIFIER | c.2063-2077C>T | FAM120C | ENSG00000184083.12 | transcript | ENST00000375180.7 | protein_coding | 9/15 | chrX | 54118871 | ||||||
chrX:54119163
|
C | T | 1 | a0001c0001t0061g0019 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.2063-2369G>A | FAM120C | ENSG00000184083.12 | transcript | ENST00000375180.7 | protein_coding | 9/15 | chrX | 54119163 | ||||||
chrX:54119211
|
C | G | 29 | a0001c0001t0001g0177a0001c0001t0002g0153a0001c0001t0002g0159others(26): Show | 30 | HG00558.hp2 HG00609.hp1 HG00621.hp1 others(27): Show |
intron_variant | MODIFIER | c.2063-2417G>C | FAM120C | ENSG00000184083.12 | transcript | ENST00000375180.7 | protein_coding | 9/15 | chrX | 54119211 | ||||||
chrX:54119214
|
A | C | 29 | a0001c0001t0001g0177a0001c0001t0002g0153a0001c0001t0002g0159others(26): Show | 30 | HG00558.hp2 HG00609.hp1 HG00621.hp1 others(27): Show |
intron_variant | MODIFIER | c.2063-2420T>G | FAM120C | ENSG00000184083.12 | transcript | ENST00000375180.7 | protein_coding | 9/15 | chrX | 54119214 | ||||||
chrX:54119337
|
TA | T | 1 | a0001c0001t0025g0146 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.2063-2544delT | FAM120C | ENSG00000184083.12 | transcript | ENST00000375180.7 | protein_coding | 9/15 | chrX | 54119337 | ||||||
chrX:54119358
|
A | G | 183 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0022others(180): Show | 185 | HG00140.hp1 HG00280.hp1 HG00558.hp1 others(182): Show |
intron_variant | MODIFIER | c.2063-2564T>C | FAM120C | ENSG00000184083.12 | transcript | ENST00000375180.7 | protein_coding | 9/15 | chrX | 54119358 | ||||||
chrX:54119400
|
T | C | 6 | a0001c0001t0018g0115a0001c0001t0018g0116a0001c0001t0018g0151others(3): Show | 6 | HG02572.hp1 HG02615.hp2 HG02809.hp2 others(3): Show |
intron_variant | MODIFIER | c.2063-2606A>G | FAM120C | ENSG00000184083.12 | transcript | ENST00000375180.7 | protein_coding | 9/15 | chrX | 54119400 | ||||||
chrX:54119483
|
T | C | 3 | a0001c0001t0022g0149a0001c0001t0043g0147a0001c0001t0045g0148 | 3 | HG02922.hp2 HG03471.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.2063-2689A>G | FAM120C | ENSG00000184083.12 | transcript | ENST00000375180.7 | protein_coding | 9/15 | chrX | 54119483 | ||||||
chrX:54119487
|
GTGT | G | 1 | a0001c0001t0022g0119 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.2063-2696_2063-269 others(7): Show |
FAM120C | ENSG00000184083.12 | transcript | ENST00000375180.7 | protein_coding | 9/15 | chrX | 54119487 | ||||||
chrX:54119532
|
C | G | 1 | a0001c0001t0001g0001 | 2 | HG01257.hp1 HG01258.hp1 |
intron_variant | MODIFIER | c.2063-2738G>C | FAM120C | ENSG00000184083.12 | transcript | ENST00000375180.7 | protein_coding | 9/15 | chrX | 54119532 | ||||||
chrX:54119533
|
G | A | 184 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0022others(181): Show | 186 | HG00140.hp1 HG00280.hp1 HG00558.hp1 others(183): Show |
intron_variant | MODIFIER | c.2063-2739C>T | FAM120C | ENSG00000184083.12 | transcript | ENST00000375180.7 | protein_coding | 9/15 | chrX | 54119533 | ||||||
chrX:54119541
|
C | T | 6 | a0001c0001t0018g0115a0001c0001t0018g0116a0001c0001t0018g0151others(3): Show | 6 | HG02572.hp1 HG02615.hp2 HG02809.hp2 others(3): Show |
intron_variant | MODIFIER | c.2063-2747G>A | FAM120C | ENSG00000184083.12 | transcript | ENST00000375180.7 | protein_coding | 9/15 | chrX | 54119541 | ||||||
chrX:54119566
|
G | GT | 1 | a0001c0001t0037g0129 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.2063-2773dupA | FAM120C | ENSG00000184083.12 | transcript | ENST00000375180.7 | protein_coding | 9/15 | chrX | 54119566 | ||||||
chrX:54119608
|
G | C | 52 | a0001c0001t0001g0177a0001c0001t0002g0132a0001c0001t0002g0153others(49): Show | 53 | HG00558.hp2 HG00609.hp1 HG00621.hp1 others(50): Show |
intron_variant | MODIFIER | c.2063-2814C>G | FAM120C | ENSG00000184083.12 | transcript | ENST00000375180.7 | protein_coding | 9/15 | chrX | 54119608 | ||||||
chrX:54119712
|
T | C | 3 | a0001c0001t0033g0012a0001c0001t0033g0013a0001c0001t0072g0106 | 3 | HG02559.hp2 HG02647.hp1 HG02809.hp1 |
intron_variant | MODIFIER | c.2063-2918A>G | FAM120C | ENSG00000184083.12 | transcript | ENST00000375180.7 | protein_coding | 9/15 | chrX | 54119712 | ||||||
chrX:54119743
|
T | G | 2 | a0001c0001t0007g0057a0001c0001t0014g0093 | 2 | HG02735.hp1 NA18943.hp1 |
intron_variant | MODIFIER | c.2063-2949A>C | FAM120C | ENSG00000184083.12 | transcript | ENST00000375180.7 | protein_coding | 9/15 | chrX | 54119743 | ||||||
chrX:54120192
|
A | G | 1 | a0001c0001t0067g0018 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.2063-3398T>C | FAM120C | ENSG00000184083.12 | transcript | ENST00000375180.7 | protein_coding | 9/15 | chrX | 54120192 | ||||||
chrX:54120525
|
G | A | 6 | a0001c0001t0018g0115a0001c0001t0018g0116a0001c0001t0018g0151others(3): Show | 6 | HG02572.hp1 HG02615.hp2 HG02809.hp2 others(3): Show |
intron_variant | MODIFIER | c.2063-3731C>T | FAM120C | ENSG00000184083.12 | transcript | ENST00000375180.7 | protein_coding | 9/15 | chrX | 54120525 | ||||||
chrX:54120529
|
G | C | 1 | a0001c0001t0037g0129 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.2063-3735C>G | FAM120C | ENSG00000184083.12 | transcript | ENST00000375180.7 | protein_coding | 9/15 | chrX | 54120529 | ||||||
chrX:54120693
|
T | C | 1 | a0001c0001t0056g0103 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.2063-3899A>G | FAM120C | ENSG00000184083.12 | transcript | ENST00000375180.7 | protein_coding | 9/15 | chrX | 54120693 | ||||||
chrX:54120841
|
T | C | 1 | a0001c0001t0009g0073 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.2063-4047A>G | FAM120C | ENSG00000184083.12 | transcript | ENST00000375180.7 | protein_coding | 9/15 | chrX | 54120841 | ||||||
chrX:54120845
|
C | A | 3 | a0001c0001t0033g0012a0001c0001t0033g0013a0001c0001t0072g0106 | 3 | HG02559.hp2 HG02647.hp1 HG02809.hp1 |
intron_variant | MODIFIER | c.2063-4051G>T | FAM120C | ENSG00000184083.12 | transcript | ENST00000375180.7 | protein_coding | 9/15 | chrX | 54120845 | ||||||
chrX:54120928
|
G | C | 3 | a0001c0001t0033g0012a0001c0001t0033g0013a0001c0001t0072g0106 | 3 | HG02559.hp2 HG02647.hp1 HG02809.hp1 |
intron_variant | MODIFIER | c.2063-4134C>G | FAM120C | ENSG00000184083.12 | transcript | ENST00000375180.7 | protein_coding | 9/15 | chrX | 54120928 | ||||||
chrX:54121031
|
G | A | 2 | a0001c0001t0004g0045a0001c0001t0011g0163 | 2 | HG01070.hp1 HG01074.hp1 |
intron_variant | MODIFIER | c.2063-4237C>T | FAM120C | ENSG00000184083.12 | transcript | ENST00000375180.7 | protein_coding | 9/15 | chrX | 54121031 | ||||||
chrX:54121034
|
T | C | 1 | a0001c0001t0055g0048 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.2063-4240A>G | FAM120C | ENSG00000184083.12 | transcript | ENST00000375180.7 | protein_coding | 9/15 | chrX | 54121034 | ||||||
chrX:54121072
|
T | G | 1 | a0001c0001t0002g0161 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.2063-4278A>C | FAM120C | ENSG00000184083.12 | transcript | ENST00000375180.7 | protein_coding | 9/15 | chrX | 54121072 | ||||||
chrX:54121225
|
G | C | 6 | a0001c0001t0019g0120a0001c0001t0022g0119a0001c0001t0027g0117others(3): Show | 6 | HG03098.hp1 HG03486.hp2 HG03579.hp1 others(3): Show |
intron_variant | MODIFIER | c.2063-4431C>G | FAM120C | ENSG00000184083.12 | transcript | ENST00000375180.7 | protein_coding | 9/15 | chrX | 54121225 | ||||||
chrX:54121600
|
TTCTC | T | 3 | a0001c0001t0033g0012a0001c0001t0033g0013a0001c0001t0072g0106 | 3 | HG02559.hp2 HG02647.hp1 HG02809.hp1 |
intron_variant | MODIFIER | c.2063-4810_2063-480 others(8): Show |
FAM120C | ENSG00000184083.12 | transcript | ENST00000375180.7 | protein_coding | 9/15 | chrX | 54121600 | ||||||
chrX:54121613
|
T | C | 2 | a0001c0001t0004g0045a0001c0001t0011g0163 | 2 | HG01070.hp1 HG01074.hp1 |
intron_variant | MODIFIER | c.2063-4819A>G | FAM120C | ENSG00000184083.12 | transcript | ENST00000375180.7 | protein_coding | 9/15 | chrX | 54121613 | ||||||
chrX:54121658
|
C | CA | 1 | a0001c0001t0005g0095 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.2063-4865dupT | FAM120C | ENSG00000184083.12 | transcript | ENST00000375180.7 | protein_coding | 9/15 | chrX | 54121658 | ||||||
chrX:54121885
|
T | C | 1 | a0001c0001t0067g0018 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.2063-5091A>G | FAM120C | ENSG00000184083.12 | transcript | ENST00000375180.7 | protein_coding | 9/15 | chrX | 54121885 | ||||||
chrX:54121893
|
G | A | 1 | a0001c0001t0001g0025 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.2063-5099C>T | FAM120C | ENSG00000184083.12 | transcript | ENST00000375180.7 | protein_coding | 9/15 | chrX | 54121893 | ||||||
chrX:54122199
|
T | C | 2 | a0001c0001t0001g0025a0001c0001t0032g0108 | 2 | NA18973.hp1 NA18998.hp1 |
intron_variant | MODIFIER | c.2063-5405A>G | FAM120C | ENSG00000184083.12 | transcript | ENST00000375180.7 | protein_coding | 9/15 | chrX | 54122199 | ||||||
chrX:54122466
|
T | G | 1 | a0001c0001t0002g0174 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.2063-5672A>C | FAM120C | ENSG00000184083.12 | transcript | ENST00000375180.7 | protein_coding | 9/15 | chrX | 54122466 | ||||||
chrX:54122620
|
G | A | 1 | a0001c0001t0039g0150 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.2063-5826C>T | FAM120C | ENSG00000184083.12 | transcript | ENST00000375180.7 | protein_coding | 9/15 | chrX | 54122620 | ||||||
chrX:54122776
|
G | T | 177 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0022others(174): Show | 179 | HG00140.hp1 HG00280.hp1 HG00558.hp1 others(176): Show |
intron_variant | MODIFIER | c.2063-5982C>A | FAM120C | ENSG00000184083.12 | transcript | ENST00000375180.7 | protein_coding | 9/15 | chrX | 54122776 | ||||||
chrX:54122858
|
G | A | 6 | a0001c0001t0018g0115a0001c0001t0018g0116a0001c0001t0018g0151others(3): Show | 6 | HG02572.hp1 HG02615.hp2 HG02809.hp2 others(3): Show |
intron_variant | MODIFIER | c.2063-6064C>T | FAM120C | ENSG00000184083.12 | transcript | ENST00000375180.7 | protein_coding | 9/15 | chrX | 54122858 | ||||||
chrX:54122861
|
C | T | 9 | a0001c0001t0018g0115a0001c0001t0018g0116a0001c0001t0018g0151others(6): Show | 9 | HG02559.hp2 HG02572.hp1 HG02615.hp2 others(6): Show |
intron_variant | MODIFIER | c.2063-6067G>A | FAM120C | ENSG00000184083.12 | transcript | ENST00000375180.7 | protein_coding | 9/15 | chrX | 54122861 | ||||||
chrX:54122881
|
G | A | 1 | a0001c0001t0013g0130 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.2063-6087C>T | FAM120C | ENSG00000184083.12 | transcript | ENST00000375180.7 | protein_coding | 9/15 | chrX | 54122881 | ||||||
chrX:54122949
|
A | G | 1 | a0001c0001t0004g0180 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.2063-6155T>C | FAM120C | ENSG00000184083.12 | transcript | ENST00000375180.7 | protein_coding | 9/15 | chrX | 54122949 | ||||||
chrX:54123000
|
G | A | 1 | a0001c0001t0048g0126 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.2063-6206C>T | FAM120C | ENSG00000184083.12 | transcript | ENST00000375180.7 | protein_coding | 9/15 | chrX | 54123000 | ||||||
chrX:54123232
|
G | A | 6 | a0001c0001t0018g0115a0001c0001t0018g0116a0001c0001t0018g0151others(3): Show | 6 | HG02572.hp1 HG02615.hp2 HG02809.hp2 others(3): Show |
intron_variant | MODIFIER | c.2063-6438C>T | FAM120C | ENSG00000184083.12 | transcript | ENST00000375180.7 | protein_coding | 9/15 | chrX | 54123232 | ||||||
chrX:54123364
|
C | T | 3 | a0001c0001t0022g0119a0003c0003t0013g0121a0003c0003t0013g0122 | 3 | HG03098.hp1 HG03579.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.2063-6570G>A | FAM120C | ENSG00000184083.12 | transcript | ENST00000375180.7 | protein_coding | 9/15 | chrX | 54123364 | ||||||
chrX:54123365
|
G | A | 3 | a0001c0001t0033g0012a0001c0001t0033g0013a0001c0001t0072g0106 | 3 | HG02559.hp2 HG02647.hp1 HG02809.hp1 |
intron_variant | MODIFIER | c.2063-6571C>T | FAM120C | ENSG00000184083.12 | transcript | ENST00000375180.7 | protein_coding | 9/15 | chrX | 54123365 | ||||||
chrX:54123381
|
C | G | 1 | a0001c0001t0010g0092 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.2063-6587G>C | FAM120C | ENSG00000184083.12 | transcript | ENST00000375180.7 | protein_coding | 9/15 | chrX | 54123381 | ||||||
chrX:54123451
|
T | C | 1 | a0001c0001t0020g0002 | 2 | HG01934.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.2063-6657A>G | FAM120C | ENSG00000184083.12 | transcript | ENST00000375180.7 | protein_coding | 9/15 | chrX | 54123451 | ||||||
chrX:54123721
|
T | A | 1 | a0001c0001t0003g0040 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.2063-6927A>T | FAM120C | ENSG00000184083.12 | transcript | ENST00000375180.7 | protein_coding | 9/15 | chrX | 54123721 | ||||||
chrX:54124030
|
C | CG | 1 | a0001c0001t0036g0078 | 1 | HG01169.hp2 | intron_variant | MODIFIER | c.2063-7237dupC | FAM120C | ENSG00000184083.12 | transcript | ENST00000375180.7 | protein_coding | 9/15 | chrX | 54124030 | ||||||
chrX:54124039
|
G | A | 6 | a0001c0001t0015g0133a0001c0001t0015g0136a0001c0001t0022g0149others(3): Show | 6 | HG02630.hp2 HG02895.hp1 HG02896.hp1 others(3): Show |
intron_variant | MODIFIER | c.2063-7245C>T | FAM120C | ENSG00000184083.12 | transcript | ENST00000375180.7 | protein_coding | 9/15 | chrX | 54124039 | ||||||
chrX:54124041
|
G | C | 1 | a0001c0001t0022g0016 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.2063-7247C>G | FAM120C | ENSG00000184083.12 | transcript | ENST00000375180.7 | protein_coding | 9/15 | chrX | 54124041 | ||||||
chrX:54124094
|
G | A | 1 | a0001c0001t0002g0168 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.2063-7300C>T | FAM120C | ENSG00000184083.12 | transcript | ENST00000375180.7 | protein_coding | 9/15 | chrX | 54124094 | ||||||
chrX:54124283
|
C | T | 1 | a0001c0001t0019g0120 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.2063-7489G>A | FAM120C | ENSG00000184083.12 | transcript | ENST00000375180.7 | protein_coding | 9/15 | chrX | 54124283 | ||||||
chrX:54124297
|
G | A | 1 | a0001c0001t0029g0088 | 1 | HG03492.hp1 | intron_variant | MODIFIER | c.2063-7503C>T | FAM120C | ENSG00000184083.12 | transcript | ENST00000375180.7 | protein_coding | 9/15 | chrX | 54124297 | ||||||
chrX:54124382
|
G | T | 1 | a0001c0001t0002g0153 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.2063-7588C>A | FAM120C | ENSG00000184083.12 | transcript | ENST00000375180.7 | protein_coding | 9/15 | chrX | 54124382 | ||||||
chrX:54124460
|
C | T | 2 | a0001c0001t0002g0132a0001c0001t0020g0131 | 2 | HG01081.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.2063-7666G>A | FAM120C | ENSG00000184083.12 | transcript | ENST00000375180.7 | protein_coding | 9/15 | chrX | 54124460 | ||||||
chrX:54124467
|
G | A | 1 | a0005c0007t0034g0007 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.2063-7673C>T | FAM120C | ENSG00000184083.12 | transcript | ENST00000375180.7 | protein_coding | 9/15 | chrX | 54124467 | ||||||
chrX:54124543
|
TC | T | 1 | a0005c0007t0034g0007 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.2063-7750delG | FAM120C | ENSG00000184083.12 | transcript | ENST00000375180.7 | protein_coding | 9/15 | chrX | 54124543 | ||||||
chrX:54124596
|
A | T | 3 | a0001c0001t0016g0137a0001c0001t0016g0141a0001c0001t0016g0142 | 3 | HG02055.hp1 HG02451.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.2063-7802T>A | FAM120C | ENSG00000184083.12 | transcript | ENST00000375180.7 | protein_coding | 9/15 | chrX | 54124596 | ||||||
chrX:54124607
|
C | T | 178 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0022others(175): Show | 180 | HG00140.hp1 HG00280.hp1 HG00558.hp1 others(177): Show |
intron_variant | MODIFIER | c.2063-7813G>A | FAM120C | ENSG00000184083.12 | transcript | ENST00000375180.7 | protein_coding | 9/15 | chrX | 54124607 | ||||||
chrX:54125007
|
C | CA | 1 | a0005c0007t0034g0007 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.2062+7684dupT | FAM120C | ENSG00000184083.12 | transcript | ENST00000375180.7 | protein_coding | 9/15 | chrX | 54125007 | ||||||
chrX:54125105
|
A | AG | 1 | a0005c0007t0034g0007 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.2062+7586dupC | FAM120C | ENSG00000184083.12 | transcript | ENST00000375180.7 | protein_coding | 9/15 | chrX | 54125105 | ||||||
chrX:54125130
|
GC | G | 1 | a0005c0007t0034g0007 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.2062+7561delG | FAM120C | ENSG00000184083.12 | transcript | ENST00000375180.7 | protein_coding | 9/15 | chrX | 54125130 | ||||||
chrX:54125208
|
C | CA | 8 | a0001c0001t0003g0107a0001c0001t0017g0176a0001c0001t0022g0149others(5): Show | 8 | HG02257.hp2 HG03453.hp1 HG03516.hp1 others(5): Show |
intron_variant | MODIFIER | c.2062+7483dupT | FAM120C | ENSG00000184083.12 | transcript | ENST00000375180.7 | protein_coding | 9/15 | chrX | 54125208 | ||||||
chrX:54125208
|
CA | C | 5 | a0001c0001t0003g0084a0001c0001t0008g0162a0001c0001t0009g0049others(2): Show | 5 | HG01257.hp2 HG02615.hp1 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.2062+7483delT | FAM120C | ENSG00000184083.12 | transcript | ENST00000375180.7 | protein_coding | 9/15 | chrX | 54125208 | ||||||
chrX:54125389
|
A | ACC | 1 | a0005c0007t0034g0007 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.2062+7302_2062+730 others(6): Show |
FAM120C | ENSG00000184083.12 | transcript | ENST00000375180.7 | protein_coding | 9/15 | chrX | 54125389 | ||||||
chrX:54125438
|
AC | A | 1 | a0005c0007t0034g0007 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.2062+7253delG | FAM120C | ENSG00000184083.12 | transcript | ENST00000375180.7 | protein_coding | 9/15 | chrX | 54125438 | ||||||
chrX:54125464
|
TA | T | 1 | a0005c0007t0034g0007 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.2062+7227delT | FAM120C | ENSG00000184083.12 | transcript | ENST00000375180.7 | protein_coding | 9/15 | chrX | 54125464 | ||||||
chrX:54125494
|
T | TG | 1 | a0001c0001t0005g0095 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.2062+7197dupC | FAM120C | ENSG00000184083.12 | transcript | ENST00000375180.7 | protein_coding | 9/15 | chrX | 54125494 | ||||||
chrX:54125662
|
C | CT | 1 | a0001c0001t0005g0095 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.2062+7029dupA | FAM120C | ENSG00000184083.12 | transcript | ENST00000375180.7 | protein_coding | 9/15 | chrX | 54125662 | ||||||
chrX:54125684
|
CA | C | 1 | a0005c0007t0034g0007 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.2062+7007delT | FAM120C | ENSG00000184083.12 | transcript | ENST00000375180.7 | protein_coding | 9/15 | chrX | 54125684 | ||||||
chrX:54125729
|
A | G | 1 | a0001c0001t0003g0181 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.2062+6963T>C | FAM120C | ENSG00000184083.12 | transcript | ENST00000375180.7 | protein_coding | 9/15 | chrX | 54125729 | ||||||
chrX:54125989
|
C | CT | 1 | a0001c0001t0005g0095 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.2062+6702dupA | FAM120C | ENSG00000184083.12 | transcript | ENST00000375180.7 | protein_coding | 9/15 | chrX | 54125989 | ||||||
chrX:54126208
|
G | C | 1 | a0001c0001t0067g0018 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.2062+6484C>G | FAM120C | ENSG00000184083.12 | transcript | ENST00000375180.7 | protein_coding | 9/15 | chrX | 54126208 | ||||||
chrX:54126222
|
GC | G | 1 | a0001c0001t0005g0113 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.2062+6469delG | FAM120C | ENSG00000184083.12 | transcript | ENST00000375180.7 | protein_coding | 9/15 | chrX | 54126222 | ||||||
chrX:54126295
|
G | GA | 1 | a0001c0001t0005g0095 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.2062+6396dupT | FAM120C | ENSG00000184083.12 | transcript | ENST00000375180.7 | protein_coding | 9/15 | chrX | 54126295 | ||||||
chrX:54126450
|
A | T | 6 | a0001c0001t0018g0115a0001c0001t0018g0116a0001c0001t0018g0151others(3): Show | 6 | HG02572.hp1 HG02615.hp2 HG02809.hp2 others(3): Show |
intron_variant | MODIFIER | c.2062+6242T>A | FAM120C | ENSG00000184083.12 | transcript | ENST00000375180.7 | protein_coding | 9/15 | chrX | 54126450 | ||||||
chrX:54126467
|
A | AG | 1 | a0001c0001t0005g0095 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.2062+6224dupC | FAM120C | ENSG00000184083.12 | transcript | ENST00000375180.7 | protein_coding | 9/15 | chrX | 54126467 | ||||||
chrX:54126664
|
CA | C | 1 | a0005c0007t0034g0007 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.2062+6027delT | FAM120C | ENSG00000184083.12 | transcript | ENST00000375180.7 | protein_coding | 9/15 | chrX | 54126664 | ||||||
chrX:54126794
|
G | A | 2 | a0001c0001t0015g0015a0001c0001t0022g0016 | 2 | HG01884.hp1 HG02717.hp1 |
intron_variant | MODIFIER | c.2062+5898C>T | FAM120C | ENSG00000184083.12 | transcript | ENST00000375180.7 | protein_coding | 9/15 | chrX | 54126794 | ||||||
chrX:54126837
|
TC | T | 1 | a0005c0007t0034g0007 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.2062+5854delG | FAM120C | ENSG00000184083.12 | transcript | ENST00000375180.7 | protein_coding | 9/15 | chrX | 54126837 | ||||||
chrX:54126969
|
CG | C | 1 | a0001c0001t0024g0080 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.2062+5722delC | FAM120C | ENSG00000184083.12 | transcript | ENST00000375180.7 | protein_coding | 9/15 | chrX | 54126969 | ||||||
chrX:54127098
|
TA | T | 1 | a0005c0007t0034g0007 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.2062+5593delT | FAM120C | ENSG00000184083.12 | transcript | ENST00000375180.7 | protein_coding | 9/15 | chrX | 54127098 | ||||||
chrX:54127316
|
G | A | 1 | a0001c0001t0050g0051 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.2062+5376C>T | FAM120C | ENSG00000184083.12 | transcript | ENST00000375180.7 | protein_coding | 9/15 | chrX | 54127316 | ||||||
chrX:54127359
|
AGGCGGGC others(16): Show |
A | 1 | a0005c0007t0034g0007 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.2062+5310_2062+533 others(27): Show |
FAM120C | ENSG00000184083.12 | transcript | ENST00000375180.7 | protein_coding | 9/15 | chrX | 54127359 | ||||||
chrX:54127435
|
C | CA | 1 | a0001c0001t0005g0095 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.2062+5256dupT | FAM120C | ENSG00000184083.12 | transcript | ENST00000375180.7 | protein_coding | 9/15 | chrX | 54127435 | ||||||
chrX:54127447
|
C | T | 1 | a0001c0001t0072g0106 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.2062+5245G>A | FAM120C | ENSG00000184083.12 | transcript | ENST00000375180.7 | protein_coding | 9/15 | chrX | 54127447 | ||||||
chrX:54127510
|
G | GA | 1 | a0001c0001t0005g0095 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.2062+5181dupT | FAM120C | ENSG00000184083.12 | transcript | ENST00000375180.7 | protein_coding | 9/15 | chrX | 54127510 | ||||||
chrX:54127545
|
T | C | 1 | a0001c0001t0029g0068 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.2062+5147A>G | FAM120C | ENSG00000184083.12 | transcript | ENST00000375180.7 | protein_coding | 9/15 | chrX | 54127545 | ||||||
chrX:54127584
|
C | CA | 13 | a0001c0001t0001g0061a0001c0001t0004g0086a0001c0001t0005g0095others(10): Show | 13 | HG01928.hp1 HG02055.hp1 HG02074.hp1 others(10): Show |
intron_variant | MODIFIER | c.2062+5107dupT | FAM120C | ENSG00000184083.12 | transcript | ENST00000375180.7 | protein_coding | 9/15 | chrX | 54127584 | ||||||
chrX:54127584
|
CA | C | 9 | a0001c0001t0009g0049a0001c0001t0009g0073a0001c0001t0017g0171others(6): Show | 9 | HG00609.hp1 HG01167.hp1 HG02257.hp2 others(6): Show |
intron_variant | MODIFIER | c.2062+5107delT | FAM120C | ENSG00000184083.12 | transcript | ENST00000375180.7 | protein_coding | 9/15 | chrX | 54127584 | ||||||
chrX:54127585
|
A | AC | 1 | a0002c0002t0007g0184 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.2062+5106_2062+510 others(5): Show |
FAM120C | ENSG00000184083.12 | transcript | ENST00000375180.7 | protein_coding | 9/15 | chrX | 54127585 | ||||||
chrX:54127663
|
T | C | 184 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0022others(181): Show | 186 | HG00140.hp1 HG00280.hp1 HG00558.hp1 others(183): Show |
intron_variant | MODIFIER | c.2062+5029A>G | FAM120C | ENSG00000184083.12 | transcript | ENST00000375180.7 | protein_coding | 9/15 | chrX | 54127663 | ||||||
chrX:54127765
|
A | AT | 1 | a0001c0001t0010g0023 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.2062+4926dupA | FAM120C | ENSG00000184083.12 | transcript | ENST00000375180.7 | protein_coding | 9/15 | chrX | 54127765 | ||||||
chrX:54127827
|
C | T | 1 | a0001c0001t0004g0180 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.2062+4865G>A | FAM120C | ENSG00000184083.12 | transcript | ENST00000375180.7 | protein_coding | 9/15 | chrX | 54127827 | ||||||
chrX:54127866
|
T | TACAGACG others(25): Show |
1 | a0001c0001t0005g0095 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.2062+4794_2062+482 others(36): Show |
FAM120C | ENSG00000184083.12 | transcript | ENST00000375180.7 | protein_coding | 9/15 | chrX | 54127866 | ||||||
chrX:54128476
|
C | CT | 1 | a0001c0001t0021g0014 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.2062+4215dupA | FAM120C | ENSG00000184083.12 | transcript | ENST00000375180.7 | protein_coding | 9/15 | chrX | 54128476 | ||||||
chrX:54128476
|
CT | C | 5 | a0001c0001t0002g0132a0001c0001t0010g0072a0001c0001t0017g0005others(2): Show | 5 | HG01081.hp1 HG01169.hp1 HG06807.hp1 others(2): Show |
intron_variant | MODIFIER | c.2062+4215delA | FAM120C | ENSG00000184083.12 | transcript | ENST00000375180.7 | protein_coding | 9/15 | chrX | 54128476 | ||||||
chrX:54128515
|
C | T | 1 | a0001c0001t0024g0080 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.2062+4177G>A | FAM120C | ENSG00000184083.12 | transcript | ENST00000375180.7 | protein_coding | 9/15 | chrX | 54128515 | ||||||
chrX:54128662
|
G | T | 1 | a0001c0001t0019g0120 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.2062+4030C>A | FAM120C | ENSG00000184083.12 | transcript | ENST00000375180.7 | protein_coding | 9/15 | chrX | 54128662 | ||||||
chrX:54128783
|
TG | T | 1 | a0001c0001t0066g0076 | 1 | NA19089.hp1 | intron_variant | MODIFIER | c.2062+3908delC | FAM120C | ENSG00000184083.12 | transcript | ENST00000375180.7 | protein_coding | 9/15 | chrX | 54128783 | ||||||
chrX:54128883
|
A | T | 1 | a0001c0001t0008g0124 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.2062+3809T>A | FAM120C | ENSG00000184083.12 | transcript | ENST00000375180.7 | protein_coding | 9/15 | chrX | 54128883 | ||||||
chrX:54128964
|
C | T | 3 | a0001c0001t0005g0037a0001c0001t0005g0058a0001c0001t0005g0095 | 3 | NA18983.hp1 NA18985.hp1 NA19000.hp1 |
intron_variant | MODIFIER | c.2062+3728G>A | FAM120C | ENSG00000184083.12 | transcript | ENST00000375180.7 | protein_coding | 9/15 | chrX | 54128964 | ||||||
chrX:54129049
|
CG | C | 1 | a0001c0001t0066g0076 | 1 | NA19089.hp1 | intron_variant | MODIFIER | c.2062+3642delC | FAM120C | ENSG00000184083.12 | transcript | ENST00000375180.7 | protein_coding | 9/15 | chrX | 54129049 | ||||||
chrX:54129070
|
TC | T | 1 | a0001c0001t0066g0076 | 1 | NA19089.hp1 | intron_variant | MODIFIER | c.2062+3621delG | FAM120C | ENSG00000184083.12 | transcript | ENST00000375180.7 | protein_coding | 9/15 | chrX | 54129070 | ||||||
chrX:54129090
|
CG | C | 1 | a0001c0001t0066g0076 | 1 | NA19089.hp1 | intron_variant | MODIFIER | c.2062+3601delC | FAM120C | ENSG00000184083.12 | transcript | ENST00000375180.7 | protein_coding | 9/15 | chrX | 54129090 | ||||||
chrX:54129104
|
A | AC | 1 | a0001c0001t0005g0011 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.2062+3587dupG | FAM120C | ENSG00000184083.12 | transcript | ENST00000375180.7 | protein_coding | 9/15 | chrX | 54129104 | ||||||
chrX:54129122
|
G | A | 29 | a0001c0001t0001g0177a0001c0001t0002g0153a0001c0001t0002g0159others(26): Show | 30 | HG00558.hp2 HG00609.hp1 HG00621.hp1 others(27): Show |
intron_variant | MODIFIER | c.2062+3570C>T | FAM120C | ENSG00000184083.12 | transcript | ENST00000375180.7 | protein_coding | 9/15 | chrX | 54129122 | ||||||
chrX:54129124
|
ACGGGGCG others(6): Show |
A | 1 | a0001c0001t0004g0071 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.2062+3555_2062+356 others(17): Show |
FAM120C | ENSG00000184083.12 | transcript | ENST00000375180.7 | protein_coding | 9/15 | chrX | 54129124 | ||||||
chrX:54129125
|
C | CG | 1 | a0001c0001t0005g0011 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.2062+3566dupC | FAM120C | ENSG00000184083.12 | transcript | ENST00000375180.7 | protein_coding | 9/15 | chrX | 54129125 | ||||||
chrX:54129138
|
C | CG | 1 | a0001c0001t0066g0076 | 1 | NA19089.hp1 | intron_variant | MODIFIER | c.2062+3553dupC | FAM120C | ENSG00000184083.12 | transcript | ENST00000375180.7 | protein_coding | 9/15 | chrX | 54129138 | ||||||
chrX:54129170
|
A | G | 178 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0022others(175): Show | 180 | HG00140.hp1 HG00280.hp1 HG00558.hp1 others(177): Show |
intron_variant | MODIFIER | c.2062+3522T>C | FAM120C | ENSG00000184083.12 | transcript | ENST00000375180.7 | protein_coding | 9/15 | chrX | 54129170 | ||||||
chrX:54129181
|
G | A | 1 | a0001c0001t0003g0040 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.2062+3511C>T | FAM120C | ENSG00000184083.12 | transcript | ENST00000375180.7 | protein_coding | 9/15 | chrX | 54129181 | ||||||
chrX:54129184
|
C | A | 2 | a0001c0001t0010g0091a0001c0001t0010g0092 | 2 | NA18612.hp1 NA18967.hp1 |
intron_variant | MODIFIER | c.2062+3508G>T | FAM120C | ENSG00000184083.12 | transcript | ENST00000375180.7 | protein_coding | 9/15 | chrX | 54129184 | ||||||
chrX:54129219
|
C | T | 1 | a0001c0001t0072g0106 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.2062+3473G>A | FAM120C | ENSG00000184083.12 | transcript | ENST00000375180.7 | protein_coding | 9/15 | chrX | 54129219 | ||||||
chrX:54129224
|
C | T | 1 | a0001c0001t0004g0006 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.2062+3468G>A | FAM120C | ENSG00000184083.12 | transcript | ENST00000375180.7 | protein_coding | 9/15 | chrX | 54129224 | ||||||
chrX:54129269
|
C | T | 2 | a0001c0001t0058g0020a0001c0001t0061g0019 | 2 | HG01069.hp1 HG01952.hp1 |
intron_variant | MODIFIER | c.2062+3423G>A | FAM120C | ENSG00000184083.12 | transcript | ENST00000375180.7 | protein_coding | 9/15 | chrX | 54129269 | ||||||
chrX:54129340
|
C | CG | 3 | a0001c0001t0002g0153a0001c0001t0003g0107a0001c0001t0026g0101 | 3 | HG03710.hp1 NA19030.hp1 NA19078.hp2 |
intron_variant | MODIFIER | c.2062+3351dupC | FAM120C | ENSG00000184083.12 | transcript | ENST00000375180.7 | protein_coding | 9/15 | chrX | 54129340 | ||||||
chrX:54129380
|
C | T | 55 | a0001c0001t0001g0022a0001c0001t0001g0060a0001c0001t0001g0061others(52): Show | 55 | HG00280.hp1 HG00558.hp1 HG00642.hp1 others(52): Show |
intron_variant | MODIFIER | c.2062+3312G>A | FAM120C | ENSG00000184083.12 | transcript | ENST00000375180.7 | protein_coding | 9/15 | chrX | 54129380 | ||||||
chrX:54129478
|
C | T | 1 | a0001c0001t0026g0101 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.2062+3214G>A | FAM120C | ENSG00000184083.12 | transcript | ENST00000375180.7 | protein_coding | 9/15 | chrX | 54129478 | ||||||
chrX:54129497
|
C | G | 187 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0022others(184): Show | 189 | HG00140.hp1 HG00280.hp1 HG00558.hp1 others(186): Show |
intron_variant | MODIFIER | c.2062+3195G>C | FAM120C | ENSG00000184083.12 | transcript | ENST00000375180.7 | protein_coding | 9/15 | chrX | 54129497 | ||||||
chrX:54129528
|
T | C | 1 | a0001c0001t0012g0043 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.2062+3164A>G | FAM120C | ENSG00000184083.12 | transcript | ENST00000375180.7 | protein_coding | 9/15 | chrX | 54129528 | ||||||
chrX:54129613
|
G | A | 53 | a0001c0001t0001g0177a0001c0001t0002g0132a0001c0001t0002g0153others(50): Show | 54 | HG00558.hp2 HG00609.hp1 HG00621.hp1 others(51): Show |
intron_variant | MODIFIER | c.2062+3079C>T | FAM120C | ENSG00000184083.12 | transcript | ENST00000375180.7 | protein_coding | 9/15 | chrX | 54129613 | ||||||
chrX:54129625
|
A | G | 1 | a0001c0001t0013g0130 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.2062+3067T>C | FAM120C | ENSG00000184083.12 | transcript | ENST00000375180.7 | protein_coding | 9/15 | chrX | 54129625 | ||||||
chrX:54129648
|
C | CT | 1 | a0006c0006t0001g0128 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.2062+3043dupA | FAM120C | ENSG00000184083.12 | transcript | ENST00000375180.7 | protein_coding | 9/15 | chrX | 54129648 | ||||||
chrX:54129672
|
TG | T | 1 | a0001c0001t0066g0076 | 1 | NA19089.hp1 | intron_variant | MODIFIER | c.2062+3019delC | FAM120C | ENSG00000184083.12 | transcript | ENST00000375180.7 | protein_coding | 9/15 | chrX | 54129672 | ||||||
chrX:54129748
|
G | A | 3 | a0001c0001t0033g0012a0001c0001t0033g0013a0001c0001t0072g0106 | 3 | HG02559.hp2 HG02647.hp1 HG02809.hp1 |
intron_variant | MODIFIER | c.2062+2944C>T | FAM120C | ENSG00000184083.12 | transcript | ENST00000375180.7 | protein_coding | 9/15 | chrX | 54129748 | ||||||
chrX:54129839
|
G | A | 1 | a0001c0001t0003g0110 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.2062+2853C>T | FAM120C | ENSG00000184083.12 | transcript | ENST00000375180.7 | protein_coding | 9/15 | chrX | 54129839 | ||||||
chrX:54129912
|
C | T | 1 | a0001c0001t0046g0085 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.2062+2780G>A | FAM120C | ENSG00000184083.12 | transcript | ENST00000375180.7 | protein_coding | 9/15 | chrX | 54129912 | ||||||
chrX:54129950
|
A | T | 1 | a0001c0001t0029g0068 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.2062+2742T>A | FAM120C | ENSG00000184083.12 | transcript | ENST00000375180.7 | protein_coding | 9/15 | chrX | 54129950 | ||||||
chrX:54129951
|
G | T | 1 | a0001c0001t0029g0068 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.2062+2741C>A | FAM120C | ENSG00000184083.12 | transcript | ENST00000375180.7 | protein_coding | 9/15 | chrX | 54129951 | ||||||
chrX:54130034
|
GGGGAGA | G | 3 | a0001c0001t0016g0137a0001c0001t0016g0141a0001c0001t0016g0142 | 3 | HG02055.hp1 HG02451.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.2062+2652_2062+265 others(10): Show |
FAM120C | ENSG00000184083.12 | transcript | ENST00000375180.7 | protein_coding | 9/15 | chrX | 54130034 | ||||||
chrX:54130098
|
GGGGAGA | G | 1 | a0001c0001t0072g0106 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.2062+2588_2062+259 others(10): Show |
FAM120C | ENSG00000184083.12 | transcript | ENST00000375180.7 | protein_coding | 9/15 | chrX | 54130098 | ||||||
chrX:54130133
|
GGGGAGA | G | 1 | a0001c0001t0033g0013 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.2062+2553_2062+255 others(10): Show |
FAM120C | ENSG00000184083.12 | transcript | ENST00000375180.7 | protein_coding | 9/15 | chrX | 54130133 | ||||||
chrX:54130133
|
GGGGAGAG others(5): Show |
G | 1 | a0001c0001t0014g0094 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.2062+2547_2062+255 others(16): Show |
FAM120C | ENSG00000184083.12 | transcript | ENST00000375180.7 | protein_coding | 9/15 | chrX | 54130133 | ||||||
chrX:54130223
|
G | GA | 1 | a0001c0001t0066g0076 | 1 | NA19089.hp1 | intron_variant | MODIFIER | c.2062+2468dupT | FAM120C | ENSG00000184083.12 | transcript | ENST00000375180.7 | protein_coding | 9/15 | chrX | 54130223 | ||||||
chrX:54130342
|
CA | C | 1 | a0001c0001t0066g0076 | 1 | NA19089.hp1 | intron_variant | MODIFIER | c.2062+2349delT | FAM120C | ENSG00000184083.12 | transcript | ENST00000375180.7 | protein_coding | 9/15 | chrX | 54130342 | ||||||
chrX:54130860
|
G | A | 2 | a0001c0001t0015g0015a0001c0001t0022g0016 | 2 | HG01884.hp1 HG02717.hp1 |
intron_variant | MODIFIER | c.2062+1832C>T | FAM120C | ENSG00000184083.12 | transcript | ENST00000375180.7 | protein_coding | 9/15 | chrX | 54130860 | ||||||
chrX:54130898
|
GC | G | 1 | a0001c0001t0066g0076 | 1 | NA19089.hp1 | intron_variant | MODIFIER | c.2062+1793delG | FAM120C | ENSG00000184083.12 | transcript | ENST00000375180.7 | protein_coding | 9/15 | chrX | 54130898 | ||||||
chrX:54130928
|
C | T | 184 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0022others(181): Show | 186 | HG00140.hp1 HG00280.hp1 HG00558.hp1 others(183): Show |
intron_variant | MODIFIER | c.2062+1764G>A | FAM120C | ENSG00000184083.12 | transcript | ENST00000375180.7 | protein_coding | 9/15 | chrX | 54130928 | ||||||
chrX:54131222
|
G | C | 1 | a0001c0001t0002g0153 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.2062+1470C>G | FAM120C | ENSG00000184083.12 | transcript | ENST00000375180.7 | protein_coding | 9/15 | chrX | 54131222 | ||||||
chrX:54131435
|
A | AT | 6 | a0001c0001t0002g0153a0001c0001t0007g0081a0001c0001t0013g0112others(3): Show | 6 | HG00738.hp1 HG02630.hp1 HG03516.hp2 others(3): Show |
intron_variant | MODIFIER | c.2062+1256dupA | FAM120C | ENSG00000184083.12 | transcript | ENST00000375180.7 | protein_coding | 9/15 | chrX | 54131435 | ||||||
chrX:54131435
|
A | ATTTTTTT others(98): Show |
1 | a0001c0001t0031g0138 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.2062+1256_2062+125 others(109): Show |
FAM120C | ENSG00000184083.12 | transcript | ENST00000375180.7 | protein_coding | 9/15 | chrX | 54131435 | ||||||
chrX:54131435
|
AT | A | 11 | a0001c0001t0004g0045a0001c0001t0015g0133a0001c0001t0015g0136others(8): Show | 11 | HG01070.hp1 HG01167.hp1 HG01169.hp1 others(8): Show |
intron_variant | MODIFIER | c.2062+1256delA | FAM120C | ENSG00000184083.12 | transcript | ENST00000375180.7 | protein_coding | 9/15 | chrX | 54131435 | ||||||
chrX:54131542
|
G | A | 2 | a0001c0001t0003g0032a0001c0001t0012g0104 | 2 | HG02083.hp1 NA18986.hp1 |
intron_variant | MODIFIER | c.2062+1150C>T | FAM120C | ENSG00000184083.12 | transcript | ENST00000375180.7 | protein_coding | 9/15 | chrX | 54131542 | ||||||
chrX:54131600
|
G | A | 1 | a0001c0001t0052g0100 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.2062+1092C>T | FAM120C | ENSG00000184083.12 | transcript | ENST00000375180.7 | protein_coding | 9/15 | chrX | 54131600 | ||||||
chrX:54131612
|
A | G | 2 | a0003c0003t0013g0121a0003c0003t0013g0122 | 2 | HG03098.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.2062+1080T>C | FAM120C | ENSG00000184083.12 | transcript | ENST00000375180.7 | protein_coding | 9/15 | chrX | 54131612 | ||||||
chrX:54131657
|
C | T | 3 | a0001c0001t0033g0012a0001c0001t0033g0013a0001c0001t0072g0106 | 3 | HG02559.hp2 HG02647.hp1 HG02809.hp1 |
intron_variant | MODIFIER | c.2062+1035G>A | FAM120C | ENSG00000184083.12 | transcript | ENST00000375180.7 | protein_coding | 9/15 | chrX | 54131657 | ||||||
chrX:54131764
|
C | CT | 1 | a0001c0001t0019g0120 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.2062+927dupA | FAM120C | ENSG00000184083.12 | transcript | ENST00000375180.7 | protein_coding | 9/15 | chrX | 54131764 | ||||||
chrX:54131764
|
CT | C | 1 | a0001c0001t0015g0136 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.2062+927delA | FAM120C | ENSG00000184083.12 | transcript | ENST00000375180.7 | protein_coding | 9/15 | chrX | 54131764 | ||||||
chrX:54131772
|
T | C | 108 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0022others(105): Show | 109 | HG00140.hp1 HG00280.hp1 HG00558.hp1 others(106): Show |
intron_variant | MODIFIER | c.2062+920A>G | FAM120C | ENSG00000184083.12 | transcript | ENST00000375180.7 | protein_coding | 9/15 | chrX | 54131772 | ||||||
chrX:54131785
|
G | A | 4 | a0001c0001t0029g0068a0001c0001t0033g0012a0001c0001t0033g0013others(1): Show | 4 | HG02559.hp2 HG02647.hp1 HG02809.hp1 others(1): Show |
intron_variant | MODIFIER | c.2062+907C>T | FAM120C | ENSG00000184083.12 | transcript | ENST00000375180.7 | protein_coding | 9/15 | chrX | 54131785 | ||||||
chrX:54131873
|
C | T | 1 | a0001c0001t0072g0106 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.2062+819G>A | FAM120C | ENSG00000184083.12 | transcript | ENST00000375180.7 | protein_coding | 9/15 | chrX | 54131873 | ||||||
chrX:54132031
|
C | CA | 1 | a0005c0007t0034g0007 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.2062+660_2062+661i others(3): Show |
FAM120C | ENSG00000184083.12 | transcript | ENST00000375180.7 | protein_coding | 9/15 | chrX | 54132031 | ||||||
chrX:54132105
|
G | A | 1 | a0001c0001t0017g0154 | 1 | HG01257.hp2 | intron_variant | MODIFIER | c.2062+587C>T | FAM120C | ENSG00000184083.12 | transcript | ENST00000375180.7 | protein_coding | 9/15 | chrX | 54132105 | ||||||
chrX:54132174
|
GC | G | 1 | a0001c0001t0066g0076 | 1 | NA19089.hp1 | intron_variant | MODIFIER | c.2062+517delG | FAM120C | ENSG00000184083.12 | transcript | ENST00000375180.7 | protein_coding | 9/15 | chrX | 54132174 | ||||||
chrX:54132180
|
C | CA | 1 | a0005c0007t0034g0007 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.2062+511dupT | FAM120C | ENSG00000184083.12 | transcript | ENST00000375180.7 | protein_coding | 9/15 | chrX | 54132180 | ||||||
chrX:54132320
|
TG | T | 1 | a0005c0007t0034g0007 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.2062+371delC | FAM120C | ENSG00000184083.12 | transcript | ENST00000375180.7 | protein_coding | 9/15 | chrX | 54132320 | ||||||
chrX:54132380
|
G | GT | 1 | a0005c0007t0034g0007 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.2062+311dupA | FAM120C | ENSG00000184083.12 | transcript | ENST00000375180.7 | protein_coding | 9/15 | chrX | 54132380 | ||||||
chrX:54132420
|
C | T | 1 | a0002c0002t0007g0184 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.2062+272G>A | FAM120C | ENSG00000184083.12 | transcript | ENST00000375180.7 | protein_coding | 9/15 | chrX | 54132420 | ||||||
chrX:54132535
|
G | A | 1 | a0001c0001t0021g0014 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.2062+157C>T | FAM120C | ENSG00000184083.12 | transcript | ENST00000375180.7 | protein_coding | 9/15 | chrX | 54132535 | ||||||
chrX:54132597
|
G | GC | 1 | a0001c0001t0066g0076 | 1 | NA19089.hp1 | intron_variant | MODIFIER | c.2062+94_2062+95ins others(1): Show |
FAM120C | ENSG00000184083.12 | transcript | ENST00000375180.7 | protein_coding | 9/15 | chrX | 54132597 | ||||||
chrX:54132660
|
G | A | 2 | a0001c0001t0014g0093a0001c0001t0014g0094 | 2 | HG02602.hp1 HG02735.hp1 |
intron_variant | MODIFIER | c.2062+32C>T | FAM120C | ENSG00000184083.12 | transcript | ENST00000375180.7 | protein_coding | 9/15 | chrX | 54132660 | ||||||
chrX:54132892
|
A | G | 1 | a0001c0001t0002g0172 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.1891-29T>C | FAM120C | ENSG00000184083.12 | transcript | ENST00000375180.7 | protein_coding | 8/15 | chrX | 54132892 | ||||||
chrX:54132901
|
G | GT | 1 | a0005c0007t0034g0007 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.1891-39dupA | FAM120C | ENSG00000184083.12 | transcript | ENST00000375180.7 | protein_coding | 8/15 | chrX | 54132901 | ||||||
chrX:54132997
|
TA | T | 1 | a0005c0007t0034g0007 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.1891-135delT | FAM120C | ENSG00000184083.12 | transcript | ENST00000375180.7 | protein_coding | 8/15 | chrX | 54132997 | ||||||
chrX:54133053
|
AT | A | 1 | a0005c0007t0034g0007 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.1891-191delA | FAM120C | ENSG00000184083.12 | transcript | ENST00000375180.7 | protein_coding | 8/15 | chrX | 54133053 | ||||||
chrX:54133068
|
A | G | 1 | a0001c0001t0056g0103 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.1891-205T>C | FAM120C | ENSG00000184083.12 | transcript | ENST00000375180.7 | protein_coding | 8/15 | chrX | 54133068 | ||||||
chrX:54133122
|
C | T | 3 | a0001c0001t0033g0012a0001c0001t0033g0013a0001c0001t0072g0106 | 3 | HG02559.hp2 HG02647.hp1 HG02809.hp1 |
intron_variant | MODIFIER | c.1891-259G>A | FAM120C | ENSG00000184083.12 | transcript | ENST00000375180.7 | protein_coding | 8/15 | chrX | 54133122 | ||||||
chrX:54133163
|
A | AC | 1 | a0001c0001t0002g0153 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.1891-301dupG | FAM120C | ENSG00000184083.12 | transcript | ENST00000375180.7 | protein_coding | 8/15 | chrX | 54133163 | ||||||
chrX:54133182
|
T | C | 1 | a0001c0001t0035g0114 | 1 | NA18972.hp2 | intron_variant | MODIFIER | c.1891-319A>G | FAM120C | ENSG00000184083.12 | transcript | ENST00000375180.7 | protein_coding | 8/15 | chrX | 54133182 | ||||||
chrX:54133191
|
T | TA | 1 | a0005c0007t0034g0007 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.1891-329dupT | FAM120C | ENSG00000184083.12 | transcript | ENST00000375180.7 | protein_coding | 8/15 | chrX | 54133191 | ||||||
chrX:54133326
|
T | C | 1 | a0001c0001t0002g0161 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.1890+447A>G | FAM120C | ENSG00000184083.12 | transcript | ENST00000375180.7 | protein_coding | 8/15 | chrX | 54133326 | ||||||
chrX:54133354
|
CA | C | 1 | a0005c0007t0034g0007 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.1890+418delT | FAM120C | ENSG00000184083.12 | transcript | ENST00000375180.7 | protein_coding | 8/15 | chrX | 54133354 | ||||||
chrX:54133411
|
A | ATGGACAT others(1): Show |
1 | a0001c0001t0065g0083 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.1890+354_1890+361d others(10): Show |
FAM120C | ENSG00000184083.12 | transcript | ENST00000375180.7 | protein_coding | 8/15 | chrX | 54133411 | ||||||
chrX:54133449
|
TG | T | 1 | a0005c0007t0034g0007 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.1890+323delC | FAM120C | ENSG00000184083.12 | transcript | ENST00000375180.7 | protein_coding | 8/15 | chrX | 54133449 | ||||||
chrX:54133591
|
TC | T | 1 | a0005c0007t0034g0007 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.1890+181delG | FAM120C | ENSG00000184083.12 | transcript | ENST00000375180.7 | protein_coding | 8/15 | chrX | 54133591 | ||||||
chrX:54133655
|
G | GC | 1 | a0005c0007t0034g0007 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.1890+117dupG | FAM120C | ENSG00000184083.12 | transcript | ENST00000375180.7 | protein_coding | 8/15 | chrX | 54133655 | ||||||
chrX:54134200
|
GC | G | 1 | a0005c0007t0034g0007 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.1617-155delG | FAM120C | ENSG00000184083.12 | transcript | ENST00000375180.7 | protein_coding | 7/15 | chrX | 54134200 | ||||||
chrX:54134395
|
G | A | 1 | a0001c0001t0033g0013 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.1617-349C>T | FAM120C | ENSG00000184083.12 | transcript | ENST00000375180.7 | protein_coding | 7/15 | chrX | 54134395 | ||||||
chrX:54134416
|
T | TC | 1 | a0005c0007t0034g0007 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.1617-371dupG | FAM120C | ENSG00000184083.12 | transcript | ENST00000375180.7 | protein_coding | 7/15 | chrX | 54134416 | ||||||
chrX:54134511
|
CT | C | 1 | a0001c0001t0066g0076 | 1 | NA19089.hp1 | intron_variant | MODIFIER | c.1616+319delA | FAM120C | ENSG00000184083.12 | transcript | ENST00000375180.7 | protein_coding | 7/15 | chrX | 54134511 | ||||||
chrX:54134680
|
G | GA | 1 | a0005c0007t0034g0007 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.1616+150dupT | FAM120C | ENSG00000184083.12 | transcript | ENST00000375180.7 | protein_coding | 7/15 | chrX | 54134680 | ||||||
chrX:54134709
|
G | A | 1 | a0001c0001t0067g0018 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.1616+122C>T | FAM120C | ENSG00000184083.12 | transcript | ENST00000375180.7 | protein_coding | 7/15 | chrX | 54134709 | ||||||
chrX:54134746
|
T | C | 1 | a0001c0001t0033g0013 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.1616+85A>G | FAM120C | ENSG00000184083.12 | transcript | ENST00000375180.7 | protein_coding | 7/15 | chrX | 54134746 | ||||||
chrX:54135211
|
G | T | 3 | a0001c0001t0033g0012a0001c0001t0033g0013a0001c0001t0072g0106 | 3 | HG02559.hp2 HG02647.hp1 HG02809.hp1 |
intron_variant | MODIFIER | c.1336-100C>A | FAM120C | ENSG00000184083.12 | transcript | ENST00000375180.7 | protein_coding | 6/15 | chrX | 54135211 | ||||||
chrX:54135268
|
T | TC | 1 | a0005c0007t0034g0007 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.1336-158dupG | FAM120C | ENSG00000184083.12 | transcript | ENST00000375180.7 | protein_coding | 6/15 | chrX | 54135268 | ||||||
chrX:54135369
|
CT | C | 1 | a0005c0007t0034g0007 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.1335+158delA | FAM120C | ENSG00000184083.12 | transcript | ENST00000375180.7 | protein_coding | 6/15 | chrX | 54135369 | ||||||
chrX:54135407
|
TA | T | 1 | a0005c0007t0034g0007 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.1335+120delT | FAM120C | ENSG00000184083.12 | transcript | ENST00000375180.7 | protein_coding | 6/15 | chrX | 54135407 | ||||||
chrX:54135426
|
C | T | 184 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0022others(181): Show | 186 | HG00140.hp1 HG00280.hp1 HG00558.hp1 others(183): Show |
intron_variant | MODIFIER | c.1335+102G>A | FAM120C | ENSG00000184083.12 | transcript | ENST00000375180.7 | protein_coding | 6/15 | chrX | 54135426 | ||||||
chrX:54135890
|
AG | A | 1 | a0001c0001t0066g0076 | 1 | NA19089.hp1 | intron_variant | MODIFIER | c.1259-287delC | FAM120C | ENSG00000184083.12 | transcript | ENST00000375180.7 | protein_coding | 5/15 | chrX | 54135890 | ||||||
chrX:54135999
|
C | CT | 3 | a0001c0001t0035g0114a0001c0001t0049g0152a0001c0001t0066g0076 | 3 | HG02572.hp1 NA18972.hp2 NA19089.hp1 |
intron_variant | MODIFIER | c.1259-396dupA | FAM120C | ENSG00000184083.12 | transcript | ENST00000375180.7 | protein_coding | 5/15 | chrX | 54135999 | ||||||
chrX:54135999
|
C | CTT | 8 | a0001c0001t0007g0017a0001c0001t0007g0054a0001c0001t0007g0055others(5): Show | 8 | NA18747.hp1 NA18943.hp1 NA18953.hp1 others(5): Show |
intron_variant | MODIFIER | c.1259-397_1259-396d others(4): Show |
FAM120C | ENSG00000184083.12 | transcript | ENST00000375180.7 | protein_coding | 5/15 | chrX | 54135999 | ||||||
chrX:54135999
|
CT | C | 2 | a0001c0001t0004g0006a0001c0001t0016g0137 | 2 | HG02451.hp2 NA19086.hp1 |
intron_variant | MODIFIER | c.1259-396delA | FAM120C | ENSG00000184083.12 | transcript | ENST00000375180.7 | protein_coding | 5/15 | chrX | 54135999 | ||||||
chrX:54136060
|
G | A | 2 | a0001c0001t0004g0045a0001c0001t0011g0163 | 2 | HG01070.hp1 HG01074.hp1 |
intron_variant | MODIFIER | c.1258+431C>T | FAM120C | ENSG00000184083.12 | transcript | ENST00000375180.7 | protein_coding | 5/15 | chrX | 54136060 | ||||||
chrX:54136316
|
T | TA | 1 | a0001c0001t0066g0076 | 1 | NA19089.hp1 | intron_variant | MODIFIER | c.1258+174dupT | FAM120C | ENSG00000184083.12 | transcript | ENST00000375180.7 | protein_coding | 5/15 | chrX | 54136316 | ||||||
chrX:54136655
|
T | A | 1 | a0001c0001t0069g0074 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.1159-65A>T | FAM120C | ENSG00000184083.12 | transcript | ENST00000375180.7 | protein_coding | 4/15 | chrX | 54136655 | ||||||
chrX:54136943
|
T | TTTA | 3 | a0001c0001t0022g0149a0001c0001t0043g0147a0001c0001t0045g0148 | 3 | HG02922.hp2 HG03471.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.1159-356_1159-354d others(5): Show |
FAM120C | ENSG00000184083.12 | transcript | ENST00000375180.7 | protein_coding | 4/15 | chrX | 54136943 | ||||||
chrX:54136943
|
T | TTTATTAT others(2): Show |
1 | a0001c0001t0033g0012 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.1159-362_1159-354d others(11): Show |
FAM120C | ENSG00000184083.12 | transcript | ENST00000375180.7 | protein_coding | 4/15 | chrX | 54136943 | ||||||
chrX:54136943
|
T | TTTATTAT others(5): Show |
1 | a0001c0001t0033g0013 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.1159-365_1159-354d others(14): Show |
FAM120C | ENSG00000184083.12 | transcript | ENST00000375180.7 | protein_coding | 4/15 | chrX | 54136943 | ||||||
chrX:54137253
|
A | T | 1 | a0001c0001t0059g0024 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.1159-663T>A | FAM120C | ENSG00000184083.12 | transcript | ENST00000375180.7 | protein_coding | 4/15 | chrX | 54137253 | ||||||
chrX:54137481
|
TAATC | T | 6 | a0001c0001t0018g0115a0001c0001t0018g0116a0001c0001t0018g0151others(3): Show | 6 | HG02572.hp1 HG02615.hp2 HG02809.hp2 others(3): Show |
intron_variant | MODIFIER | c.1159-895_1159-892d others(6): Show |
FAM120C | ENSG00000184083.12 | transcript | ENST00000375180.7 | protein_coding | 4/15 | chrX | 54137481 | ||||||
chrX:54138092
|
G | T | 126 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0022others(123): Show | 127 | HG00140.hp1 HG00280.hp1 HG00558.hp1 others(124): Show |
intron_variant | MODIFIER | c.1159-1502C>A | FAM120C | ENSG00000184083.12 | transcript | ENST00000375180.7 | protein_coding | 4/15 | chrX | 54138092 | ||||||
chrX:54138328
|
C | T | 1 | a0001c0001t0003g0040 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.1159-1738G>A | FAM120C | ENSG00000184083.12 | transcript | ENST00000375180.7 | protein_coding | 4/15 | chrX | 54138328 | ||||||
chrX:54138495
|
C | CA | 118 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0022others(115): Show | 119 | HG00140.hp1 HG00280.hp1 HG00558.hp1 others(116): Show |
intron_variant | MODIFIER | c.1159-1906dupT | FAM120C | ENSG00000184083.12 | transcript | ENST00000375180.7 | protein_coding | 4/15 | chrX | 54138495 | ||||||
chrX:54138495
|
C | CAA | 11 | a0001c0001t0001g0052a0001c0001t0001g0079a0001c0001t0012g0104others(8): Show | 11 | HG00735.hp1 HG00735.hp2 HG01192.hp1 others(8): Show |
intron_variant | MODIFIER | c.1159-1907_1159-190 others(6): Show |
FAM120C | ENSG00000184083.12 | transcript | ENST00000375180.7 | protein_coding | 4/15 | chrX | 54138495 | ||||||
chrX:54138495
|
CA | C | 6 | a0001c0001t0008g0125a0001c0001t0018g0115a0001c0001t0018g0151others(3): Show | 6 | HG02451.hp1 HG02615.hp2 HG02809.hp2 others(3): Show |
intron_variant | MODIFIER | c.1159-1906delT | FAM120C | ENSG00000184083.12 | transcript | ENST00000375180.7 | protein_coding | 4/15 | chrX | 54138495 | ||||||
chrX:54138495
|
CAA | C | 2 | a0001c0001t0018g0116a0001c0001t0049g0152 | 2 | HG02572.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.1159-1907_1159-190 others(6): Show |
FAM120C | ENSG00000184083.12 | transcript | ENST00000375180.7 | protein_coding | 4/15 | chrX | 54138495 | ||||||
chrX:54138532
|
T | G | 2 | a0001c0001t0043g0147a0001c0001t0045g0148 | 2 | HG02922.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.1159-1942A>C | FAM120C | ENSG00000184083.12 | transcript | ENST00000375180.7 | protein_coding | 4/15 | chrX | 54138532 | ||||||
chrX:54138584
|
TG | T | 1 | a0001c0001t0004g0006 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.1159-1995delC | FAM120C | ENSG00000184083.12 | transcript | ENST00000375180.7 | protein_coding | 4/15 | chrX | 54138584 | ||||||
chrX:54138704
|
A | G | 1 | a0001c0001t0011g0155 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.1159-2114T>C | FAM120C | ENSG00000184083.12 | transcript | ENST00000375180.7 | protein_coding | 4/15 | chrX | 54138704 | ||||||
chrX:54138806
|
G | A | 5 | a0001c0001t0002g0132a0001c0001t0008g0124a0001c0001t0008g0125others(2): Show | 5 | HG01081.hp1 HG02258.hp1 HG02451.hp1 others(2): Show |
intron_variant | MODIFIER | c.1159-2216C>T | FAM120C | ENSG00000184083.12 | transcript | ENST00000375180.7 | protein_coding | 4/15 | chrX | 54138806 | ||||||
chrX:54138824
|
A | C | 1 | a0001c0001t0001g0022 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.1159-2234T>G | FAM120C | ENSG00000184083.12 | transcript | ENST00000375180.7 | protein_coding | 4/15 | chrX | 54138824 | ||||||
chrX:54138941
|
T | TC | 1 | a0001c0001t0004g0006 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.1159-2352dupG | FAM120C | ENSG00000184083.12 | transcript | ENST00000375180.7 | protein_coding | 4/15 | chrX | 54138941 | ||||||
chrX:54139316
|
AT | A | 4 | a0001c0001t0004g0006a0001c0001t0026g0101a0001c0001t0043g0147others(1): Show | 4 | HG02922.hp2 HG03471.hp1 NA19030.hp1 others(1): Show |
intron_variant | MODIFIER | c.1159-2727delA | FAM120C | ENSG00000184083.12 | transcript | ENST00000375180.7 | protein_coding | 4/15 | chrX | 54139316 | ||||||
chrX:54139329
|
T | TTTTA | 10 | a0001c0001t0013g0130a0001c0001t0015g0015a0001c0001t0020g0002others(7): Show | 11 | HG00735.hp2 HG01243.hp1 HG01884.hp1 others(8): Show |
intron_variant | MODIFIER | c.1159-2743_1159-274 others(8): Show |
FAM120C | ENSG00000184083.12 | transcript | ENST00000375180.7 | protein_coding | 4/15 | chrX | 54139329 | ||||||
chrX:54139329
|
T | TTTTATTT others(1): Show |
50 | a0001c0001t0001g0025a0001c0001t0001g0036a0001c0001t0001g0044others(47): Show | 50 | HG00140.hp1 HG00621.hp1 HG00735.hp1 others(47): Show |
intron_variant | MODIFIER | c.1159-2747_1159-274 others(12): Show |
FAM120C | ENSG00000184083.12 | transcript | ENST00000375180.7 | protein_coding | 4/15 | chrX | 54139329 | ||||||
chrX:54139329
|
T | TTTTATTT others(5): Show |
85 | a0001c0001t0001g0008a0001c0001t0001g0027a0001c0001t0001g0042others(82): Show | 85 | HG00280.hp1 HG00558.hp1 HG00558.hp2 others(82): Show |
intron_variant | MODIFIER | c.1159-2751_1159-274 others(16): Show |
FAM120C | ENSG00000184083.12 | transcript | ENST00000375180.7 | protein_coding | 4/15 | chrX | 54139329 | ||||||
chrX:54139329
|
T | TTTTATTT others(9): Show |
22 | a0001c0001t0001g0001a0001c0001t0001g0022a0001c0001t0002g0132others(19): Show | 23 | HG00673.hp1 HG01081.hp1 HG01099.hp1 others(20): Show |
intron_variant | MODIFIER | c.1159-2755_1159-274 others(20): Show |
FAM120C | ENSG00000184083.12 | transcript | ENST00000375180.7 | protein_coding | 4/15 | chrX | 54139329 | ||||||
chrX:54139329
|
T | TTTTATTT others(13): Show |
4 | a0001c0001t0001g0177a0001c0001t0010g0092a0001c0001t0037g0129others(1): Show | 4 | HG04204.hp1 NA18965.hp1 NA18967.hp1 others(1): Show |
intron_variant | MODIFIER | c.1159-2759_1159-274 others(24): Show |
FAM120C | ENSG00000184083.12 | transcript | ENST00000375180.7 | protein_coding | 4/15 | chrX | 54139329 | ||||||
chrX:54139329
|
TTTTA | T | 3 | a0001c0001t0033g0012a0001c0001t0033g0013a0001c0001t0072g0106 | 3 | HG02559.hp2 HG02647.hp1 HG02809.hp1 |
intron_variant | MODIFIER | c.1159-2743_1159-274 others(8): Show |
FAM120C | ENSG00000184083.12 | transcript | ENST00000375180.7 | protein_coding | 4/15 | chrX | 54139329 | ||||||
chrX:54139329
|
TTTTATTT others(1): Show |
T | 6 | a0001c0001t0018g0115a0001c0001t0018g0116a0001c0001t0018g0151others(3): Show | 6 | HG02572.hp1 HG02615.hp2 HG02809.hp2 others(3): Show |
intron_variant | MODIFIER | c.1159-2747_1159-274 others(12): Show |
FAM120C | ENSG00000184083.12 | transcript | ENST00000375180.7 | protein_coding | 4/15 | chrX | 54139329 | ||||||
chrX:54139465
|
G | A | 1 | a0001c0001t0003g0110 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.1159-2875C>T | FAM120C | ENSG00000184083.12 | transcript | ENST00000375180.7 | protein_coding | 4/15 | chrX | 54139465 | ||||||
chrX:54139691
|
AG | A | 1 | a0001c0001t0004g0006 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.1159-3102delC | FAM120C | ENSG00000184083.12 | transcript | ENST00000375180.7 | protein_coding | 4/15 | chrX | 54139691 | ||||||
chrX:54139851
|
C | G | 6 | a0001c0001t0018g0115a0001c0001t0018g0116a0001c0001t0018g0151others(3): Show | 6 | HG02572.hp1 HG02615.hp2 HG02809.hp2 others(3): Show |
intron_variant | MODIFIER | c.1159-3261G>C | FAM120C | ENSG00000184083.12 | transcript | ENST00000375180.7 | protein_coding | 4/15 | chrX | 54139851 | ||||||
chrX:54140153
|
G | A | 1 | a0001c0001t0024g0080 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.1159-3563C>T | FAM120C | ENSG00000184083.12 | transcript | ENST00000375180.7 | protein_coding | 4/15 | chrX | 54140153 | ||||||
chrX:54140269
|
C | T | 1 | a0001c0001t0012g0047 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.1159-3679G>A | FAM120C | ENSG00000184083.12 | transcript | ENST00000375180.7 | protein_coding | 4/15 | chrX | 54140269 | ||||||
chrX:54140291
|
C | CA | 2 | a0001c0001t0008g0170a0001c0001t0009g0070 | 2 | HG01109.hp1 NA19082.hp1 |
intron_variant | MODIFIER | c.1159-3702dupT | FAM120C | ENSG00000184083.12 | transcript | ENST00000375180.7 | protein_coding | 4/15 | chrX | 54140291 | ||||||
chrX:54140291
|
CA | C | 1 | a0001c0001t0046g0085 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.1159-3702delT | FAM120C | ENSG00000184083.12 | transcript | ENST00000375180.7 | protein_coding | 4/15 | chrX | 54140291 | ||||||
chrX:54140444
|
C | T | 10 | a0001c0001t0016g0137a0001c0001t0016g0139a0001c0001t0016g0141others(7): Show | 10 | HG01255.hp1 HG01884.hp2 HG02055.hp1 others(7): Show |
intron_variant | MODIFIER | c.1159-3854G>A | FAM120C | ENSG00000184083.12 | transcript | ENST00000375180.7 | protein_coding | 4/15 | chrX | 54140444 | ||||||
chrX:54140481
|
G | A | 1 | a0001c0001t0012g0043 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.1159-3891C>T | FAM120C | ENSG00000184083.12 | transcript | ENST00000375180.7 | protein_coding | 4/15 | chrX | 54140481 | ||||||
chrX:54140624
|
GA | G | 1 | a0001c0001t0036g0078 | 1 | HG01169.hp2 | intron_variant | MODIFIER | c.1159-4035delT | FAM120C | ENSG00000184083.12 | transcript | ENST00000375180.7 | protein_coding | 4/15 | chrX | 54140624 | ||||||
chrX:54140934
|
C | T | 1 | a0001c0001t0033g0012 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.1159-4344G>A | FAM120C | ENSG00000184083.12 | transcript | ENST00000375180.7 | protein_coding | 4/15 | chrX | 54140934 | ||||||
chrX:54140939
|
C | CA | 5 | a0001c0001t0003g0038a0001c0001t0003g0040a0001c0001t0003g0041others(2): Show | 5 | HG02572.hp1 HG04199.hp1 NA18984.hp1 others(2): Show |
intron_variant | MODIFIER | c.1159-4350dupT | FAM120C | ENSG00000184083.12 | transcript | ENST00000375180.7 | protein_coding | 4/15 | chrX | 54140939 | ||||||
chrX:54140939
|
CA | C | 6 | a0001c0001t0007g0017a0001c0001t0012g0035a0001c0001t0030g0140others(3): Show | 6 | HG01884.hp2 HG02559.hp2 HG02647.hp1 others(3): Show |
intron_variant | MODIFIER | c.1159-4350delT | FAM120C | ENSG00000184083.12 | transcript | ENST00000375180.7 | protein_coding | 4/15 | chrX | 54140939 | ||||||
chrX:54141085
|
CA | C | 1 | a0005c0007t0034g0007 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.1159-4496delT | FAM120C | ENSG00000184083.12 | transcript | ENST00000375180.7 | protein_coding | 4/15 | chrX | 54141085 | ||||||
chrX:54141524
|
G | T | 187 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0022others(184): Show | 189 | HG00140.hp1 HG00280.hp1 HG00558.hp1 others(186): Show |
intron_variant | MODIFIER | c.1159-4934C>A | FAM120C | ENSG00000184083.12 | transcript | ENST00000375180.7 | protein_coding | 4/15 | chrX | 54141524 | ||||||
chrX:54141987
|
T | C | 1 | a0001c0001t0004g0071 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.1159-5397A>G | FAM120C | ENSG00000184083.12 | transcript | ENST00000375180.7 | protein_coding | 4/15 | chrX | 54141987 | ||||||
chrX:54141995
|
T | C | 10 | a0001c0001t0016g0137a0001c0001t0016g0139a0001c0001t0016g0141others(7): Show | 10 | HG01255.hp1 HG01884.hp2 HG02055.hp1 others(7): Show |
intron_variant | MODIFIER | c.1159-5405A>G | FAM120C | ENSG00000184083.12 | transcript | ENST00000375180.7 | protein_coding | 4/15 | chrX | 54141995 | ||||||
chrX:54142036
|
C | T | 3 | a0001c0001t0003g0040a0001c0001t0003g0041a0001c0001t0012g0127 | 3 | NA18984.hp1 NA18994.hp1 NA19012.hp1 |
intron_variant | MODIFIER | c.1159-5446G>A | FAM120C | ENSG00000184083.12 | transcript | ENST00000375180.7 | protein_coding | 4/15 | chrX | 54142036 | ||||||
chrX:54142266
|
A | G | 187 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0022others(184): Show | 189 | HG00140.hp1 HG00280.hp1 HG00558.hp1 others(186): Show |
intron_variant | MODIFIER | c.1159-5676T>C | FAM120C | ENSG00000184083.12 | transcript | ENST00000375180.7 | protein_coding | 4/15 | chrX | 54142266 | ||||||
chrX:54142289
|
T | TG | 1 | a0001c0001t0005g0095 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.1159-5700dupC | FAM120C | ENSG00000184083.12 | transcript | ENST00000375180.7 | protein_coding | 4/15 | chrX | 54142289 | ||||||
chrX:54142329
|
AG | A | 1 | a0001c0001t0005g0095 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.1159-5740delC | FAM120C | ENSG00000184083.12 | transcript | ENST00000375180.7 | protein_coding | 4/15 | chrX | 54142329 | ||||||
chrX:54142444
|
C | T | 15 | a0001c0001t0013g0112a0001c0001t0015g0015a0001c0001t0015g0097others(12): Show | 15 | HG00735.hp1 HG00738.hp1 HG01243.hp1 others(12): Show |
intron_variant | MODIFIER | c.1159-5854G>A | FAM120C | ENSG00000184083.12 | transcript | ENST00000375180.7 | protein_coding | 4/15 | chrX | 54142444 | ||||||
chrX:54142517
|
G | A | 2 | a0001c0001t0058g0020a0001c0001t0061g0019 | 2 | HG01069.hp1 HG01952.hp1 |
intron_variant | MODIFIER | c.1159-5927C>T | FAM120C | ENSG00000184083.12 | transcript | ENST00000375180.7 | protein_coding | 4/15 | chrX | 54142517 | ||||||
chrX:54142618
|
A | AG | 1 | a0001c0001t0005g0095 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.1159-6029dupC | FAM120C | ENSG00000184083.12 | transcript | ENST00000375180.7 | protein_coding | 4/15 | chrX | 54142618 | ||||||
chrX:54142846
|
G | GC | 1 | a0001c0001t0005g0095 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.1159-6257dupG | FAM120C | ENSG00000184083.12 | transcript | ENST00000375180.7 | protein_coding | 4/15 | chrX | 54142846 | ||||||
chrX:54142989
|
G | C | 1 | a0001c0001t0004g0086 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.1159-6399C>G | FAM120C | ENSG00000184083.12 | transcript | ENST00000375180.7 | protein_coding | 4/15 | chrX | 54142989 | ||||||
chrX:54143026
|
T | TC | 1 | a0001c0001t0005g0095 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.1159-6437dupG | FAM120C | ENSG00000184083.12 | transcript | ENST00000375180.7 | protein_coding | 4/15 | chrX | 54143026 | ||||||
chrX:54143181
|
T | TTG | 1 | a0001c0001t0005g0095 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.1159-6592_1159-659 others(6): Show |
FAM120C | ENSG00000184083.12 | transcript | ENST00000375180.7 | protein_coding | 4/15 | chrX | 54143181 | ||||||
chrX:54143304
|
T | TA | 1 | a0001c0001t0005g0095 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.1159-6715dupT | FAM120C | ENSG00000184083.12 | transcript | ENST00000375180.7 | protein_coding | 4/15 | chrX | 54143304 | ||||||
chrX:54143317
|
A | AG | 1 | a0001c0001t0005g0095 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.1159-6728dupC | FAM120C | ENSG00000184083.12 | transcript | ENST00000375180.7 | protein_coding | 4/15 | chrX | 54143317 | ||||||
chrX:54143336
|
C | G | 152 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0022others(149): Show | 154 | HG00140.hp1 HG00280.hp1 HG00558.hp1 others(151): Show |
intron_variant | MODIFIER | c.1159-6746G>C | FAM120C | ENSG00000184083.12 | transcript | ENST00000375180.7 | protein_coding | 4/15 | chrX | 54143336 | ||||||
chrX:54143354
|
CA | C | 1 | a0001c0001t0022g0119 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.1159-6765delT | FAM120C | ENSG00000184083.12 | transcript | ENST00000375180.7 | protein_coding | 4/15 | chrX | 54143354 | ||||||
chrX:54143399
|
CA | C | 1 | a0001c0001t0005g0095 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.1159-6810delT | FAM120C | ENSG00000184083.12 | transcript | ENST00000375180.7 | protein_coding | 4/15 | chrX | 54143399 | ||||||
chrX:54143508
|
C | CA | 1 | a0001c0001t0005g0095 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.1159-6919dupT | FAM120C | ENSG00000184083.12 | transcript | ENST00000375180.7 | protein_coding | 4/15 | chrX | 54143508 | ||||||
chrX:54143644
|
TA | T | 1 | a0001c0001t0005g0095 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.1159-7055delT | FAM120C | ENSG00000184083.12 | transcript | ENST00000375180.7 | protein_coding | 4/15 | chrX | 54143644 | ||||||
chrX:54143686
|
AC | A | 1 | a0001c0001t0005g0095 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.1159-7097delG | FAM120C | ENSG00000184083.12 | transcript | ENST00000375180.7 | protein_coding | 4/15 | chrX | 54143686 | ||||||
chrX:54143818
|
G | A | 1 | a0001c0001t0067g0018 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.1159-7228C>T | FAM120C | ENSG00000184083.12 | transcript | ENST00000375180.7 | protein_coding | 4/15 | chrX | 54143818 | ||||||
chrX:54143838
|
CA | C | 1 | a0001c0001t0005g0095 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.1159-7249delT | FAM120C | ENSG00000184083.12 | transcript | ENST00000375180.7 | protein_coding | 4/15 | chrX | 54143838 | ||||||
chrX:54143860
|
A | G | 6 | a0001c0001t0018g0115a0001c0001t0018g0116a0001c0001t0018g0151others(3): Show | 6 | HG02572.hp1 HG02615.hp2 HG02809.hp2 others(3): Show |
intron_variant | MODIFIER | c.1159-7270T>C | FAM120C | ENSG00000184083.12 | transcript | ENST00000375180.7 | protein_coding | 4/15 | chrX | 54143860 | ||||||
chrX:54143902
|
C | CA | 1 | a0001c0001t0005g0095 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.1159-7313dupT | FAM120C | ENSG00000184083.12 | transcript | ENST00000375180.7 | protein_coding | 4/15 | chrX | 54143902 | ||||||
chrX:54143987
|
TG | T | 1 | a0001c0001t0005g0095 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.1158+7257delC | FAM120C | ENSG00000184083.12 | transcript | ENST00000375180.7 | protein_coding | 4/15 | chrX | 54143987 | ||||||
chrX:54143994
|
CA | C | 2 | a0001c0001t0058g0020a0001c0001t0061g0019 | 2 | HG01069.hp1 HG01952.hp1 |
intron_variant | MODIFIER | c.1158+7250delT | FAM120C | ENSG00000184083.12 | transcript | ENST00000375180.7 | protein_coding | 4/15 | chrX | 54143994 | ||||||
chrX:54144017
|
A | AC | 1 | a0001c0001t0005g0095 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.1158+7227_1158+722 others(5): Show |
FAM120C | ENSG00000184083.12 | transcript | ENST00000375180.7 | protein_coding | 4/15 | chrX | 54144017 | ||||||
chrX:54144055
|
A | AC | 1 | a0001c0001t0005g0095 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.1158+7189dupG | FAM120C | ENSG00000184083.12 | transcript | ENST00000375180.7 | protein_coding | 4/15 | chrX | 54144055 | ||||||
chrX:54144101
|
C | CA | 1 | a0001c0001t0005g0095 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.1158+7143dupT | FAM120C | ENSG00000184083.12 | transcript | ENST00000375180.7 | protein_coding | 4/15 | chrX | 54144101 | ||||||
chrX:54144125
|
A | G | 1 | a0001c0001t0065g0083 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.1158+7120T>C | FAM120C | ENSG00000184083.12 | transcript | ENST00000375180.7 | protein_coding | 4/15 | chrX | 54144125 | ||||||
chrX:54144267
|
C | T | 1 | a0002c0002t0001g0187 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.1158+6978G>A | FAM120C | ENSG00000184083.12 | transcript | ENST00000375180.7 | protein_coding | 4/15 | chrX | 54144267 | ||||||
chrX:54144409
|
G | GA | 1 | a0001c0001t0005g0095 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.1158+6835dupT | FAM120C | ENSG00000184083.12 | transcript | ENST00000375180.7 | protein_coding | 4/15 | chrX | 54144409 | ||||||
chrX:54144591
|
A | G | 6 | a0001c0001t0015g0133a0001c0001t0015g0136a0001c0001t0022g0149others(3): Show | 6 | HG02630.hp2 HG02895.hp1 HG02896.hp1 others(3): Show |
intron_variant | MODIFIER | c.1158+6654T>C | FAM120C | ENSG00000184083.12 | transcript | ENST00000375180.7 | protein_coding | 4/15 | chrX | 54144591 | ||||||
chrX:54144631
|
G | A | 1 | a0001c0001t0003g0181 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.1158+6614C>T | FAM120C | ENSG00000184083.12 | transcript | ENST00000375180.7 | protein_coding | 4/15 | chrX | 54144631 | ||||||
chrX:54144966
|
C | T | 3 | a0001c0001t0033g0012a0001c0001t0033g0013a0001c0001t0072g0106 | 3 | HG02559.hp2 HG02647.hp1 HG02809.hp1 |
intron_variant | MODIFIER | c.1158+6279G>A | FAM120C | ENSG00000184083.12 | transcript | ENST00000375180.7 | protein_coding | 4/15 | chrX | 54144966 | ||||||
chrX:54144969
|
T | C | 1 | a0001c0001t0065g0083 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.1158+6276A>G | FAM120C | ENSG00000184083.12 | transcript | ENST00000375180.7 | protein_coding | 4/15 | chrX | 54144969 | ||||||
chrX:54145057
|
C | A | 1 | a0001c0001t0067g0018 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.1158+6188G>T | FAM120C | ENSG00000184083.12 | transcript | ENST00000375180.7 | protein_coding | 4/15 | chrX | 54145057 | ||||||
chrX:54145261
|
G | A | 2 | a0001c0001t0043g0147a0001c0001t0045g0148 | 2 | HG02922.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.1158+5984C>T | FAM120C | ENSG00000184083.12 | transcript | ENST00000375180.7 | protein_coding | 4/15 | chrX | 54145261 | ||||||
chrX:54145507
|
G | T | 6 | a0001c0001t0015g0015a0001c0001t0022g0016a0001c0001t0026g0101others(3): Show | 6 | HG00735.hp1 HG01243.hp1 HG01884.hp1 others(3): Show |
intron_variant | MODIFIER | c.1158+5738C>A | FAM120C | ENSG00000184083.12 | transcript | ENST00000375180.7 | protein_coding | 4/15 | chrX | 54145507 | ||||||
chrX:54145521
|
T | G | 1 | a0001c0001t0023g0109 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.1158+5724A>C | FAM120C | ENSG00000184083.12 | transcript | ENST00000375180.7 | protein_coding | 4/15 | chrX | 54145521 | ||||||
chrX:54145913
|
T | C | 2 | a0001c0001t0010g0023a0001c0001t0010g0072 | 2 | NA18969.hp1 NA19062.hp1 |
intron_variant | MODIFIER | c.1158+5332A>G | FAM120C | ENSG00000184083.12 | transcript | ENST00000375180.7 | protein_coding | 4/15 | chrX | 54145913 | ||||||
chrX:54146006
|
A | T | 1 | a0001c0001t0026g0101 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1158+5239T>A | FAM120C | ENSG00000184083.12 | transcript | ENST00000375180.7 | protein_coding | 4/15 | chrX | 54146006 | ||||||
chrX:54146050
|
C | T | 1 | a0001c0001t0067g0018 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.1158+5195G>A | FAM120C | ENSG00000184083.12 | transcript | ENST00000375180.7 | protein_coding | 4/15 | chrX | 54146050 | ||||||
chrX:54146073
|
C | T | 1 | a0001c0001t0022g0119 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.1158+5172G>A | FAM120C | ENSG00000184083.12 | transcript | ENST00000375180.7 | protein_coding | 4/15 | chrX | 54146073 | ||||||
chrX:54146169
|
A | AG | 2 | a0001c0001t0011g0010a0001c0001t0014g0046 | 2 | HG04115.hp1 NA18980.hp1 |
intron_variant | MODIFIER | c.1158+5075dupC | FAM120C | ENSG00000184083.12 | transcript | ENST00000375180.7 | protein_coding | 4/15 | chrX | 54146169 | ||||||
chrX:54146278
|
C | T | 1 | a0001c0001t0048g0126 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.1158+4967G>A | FAM120C | ENSG00000184083.12 | transcript | ENST00000375180.7 | protein_coding | 4/15 | chrX | 54146278 | ||||||
chrX:54146306
|
TA | T | 1 | a0001c0001t0009g0034 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.1158+4938delT | FAM120C | ENSG00000184083.12 | transcript | ENST00000375180.7 | protein_coding | 4/15 | chrX | 54146306 | ||||||
chrX:54146329
|
TA | T | 2 | a0001c0001t0027g0117a0001c0001t0039g0150 | 2 | NA18522.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.1158+4915delT | FAM120C | ENSG00000184083.12 | transcript | ENST00000375180.7 | protein_coding | 4/15 | chrX | 54146329 | ||||||
chrX:54147037
|
C | T | 1 | a0001c0001t0019g0111 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.1158+4208G>A | FAM120C | ENSG00000184083.12 | transcript | ENST00000375180.7 | protein_coding | 4/15 | chrX | 54147037 | ||||||
chrX:54147147
|
C | T | 6 | a0001c0001t0018g0115a0001c0001t0018g0116a0001c0001t0018g0151others(3): Show | 6 | HG02572.hp1 HG02615.hp2 HG02809.hp2 others(3): Show |
intron_variant | MODIFIER | c.1158+4098G>A | FAM120C | ENSG00000184083.12 | transcript | ENST00000375180.7 | protein_coding | 4/15 | chrX | 54147147 | ||||||
chrX:54147316
|
CAAAT | C | 1 | a0001c0001t0026g0102 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.1158+3925_1158+392 others(8): Show |
FAM120C | ENSG00000184083.12 | transcript | ENST00000375180.7 | protein_coding | 4/15 | chrX | 54147316 | ||||||
chrX:54147540
|
G | A | 184 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0022others(181): Show | 186 | HG00140.hp1 HG00280.hp1 HG00558.hp1 others(183): Show |
intron_variant | MODIFIER | c.1158+3705C>T | FAM120C | ENSG00000184083.12 | transcript | ENST00000375180.7 | protein_coding | 4/15 | chrX | 54147540 | ||||||
chrX:54147841
|
C | T | 2 | a0001c0001t0010g0091a0001c0001t0010g0092 | 2 | NA18612.hp1 NA18967.hp1 |
intron_variant | MODIFIER | c.1158+3404G>A | FAM120C | ENSG00000184083.12 | transcript | ENST00000375180.7 | protein_coding | 4/15 | chrX | 54147841 | ||||||
chrX:54148280
|
T | A | 1 | a0002c0002t0047g0185 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.1158+2965A>T | FAM120C | ENSG00000184083.12 | transcript | ENST00000375180.7 | protein_coding | 4/15 | chrX | 54148280 | ||||||
chrX:54148363
|
T | C | 125 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0022others(122): Show | 126 | HG00140.hp1 HG00280.hp1 HG00558.hp1 others(123): Show |
intron_variant | MODIFIER | c.1158+2882A>G | FAM120C | ENSG00000184083.12 | transcript | ENST00000375180.7 | protein_coding | 4/15 | chrX | 54148363 | ||||||
chrX:54148520
|
G | A | 1 | a0001c0001t0023g0089 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.1158+2725C>T | FAM120C | ENSG00000184083.12 | transcript | ENST00000375180.7 | protein_coding | 4/15 | chrX | 54148520 | ||||||
chrX:54148621
|
T | G | 1 | a0001c0001t0022g0149 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.1158+2624A>C | FAM120C | ENSG00000184083.12 | transcript | ENST00000375180.7 | protein_coding | 4/15 | chrX | 54148621 | ||||||
chrX:54148974
|
G | GA | 1 | a0001c0001t0008g0165 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.1158+2270dupT | FAM120C | ENSG00000184083.12 | transcript | ENST00000375180.7 | protein_coding | 4/15 | chrX | 54148974 | ||||||
chrX:54149158
|
C | A | 1 | a0001c0001t0001g0001 | 2 | HG01257.hp1 HG01258.hp1 |
intron_variant | MODIFIER | c.1158+2087G>T | FAM120C | ENSG00000184083.12 | transcript | ENST00000375180.7 | protein_coding | 4/15 | chrX | 54149158 | ||||||
chrX:54149369
|
A | T | 3 | a0001c0005t0006g0004a0001c0009t0071g0031a0008c0010t0075g0188 | 3 | NA18959.hp1 NA18989.hp1 NA19055.hp1 |
intron_variant | MODIFIER | c.1158+1876T>A | FAM120C | ENSG00000184083.12 | transcript | ENST00000375180.7 | protein_coding | 4/15 | chrX | 54149369 | ||||||
chrX:54149508
|
G | A | 2 | a0001c0001t0001g0177a0001c0001t0032g0178 | 2 | NA18972.hp1 NA18973.hp2 |
intron_variant | MODIFIER | c.1158+1737C>T | FAM120C | ENSG00000184083.12 | transcript | ENST00000375180.7 | protein_coding | 4/15 | chrX | 54149508 | ||||||
chrX:54149525
|
G | C | 1 | a0001c0001t0019g0111 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.1158+1720C>G | FAM120C | ENSG00000184083.12 | transcript | ENST00000375180.7 | protein_coding | 4/15 | chrX | 54149525 | ||||||
chrX:54149639
|
CA | C | 184 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0022others(181): Show | 186 | HG00140.hp1 HG00280.hp1 HG00558.hp1 others(183): Show |
intron_variant | MODIFIER | c.1158+1605delT | FAM120C | ENSG00000184083.12 | transcript | ENST00000375180.7 | protein_coding | 4/15 | chrX | 54149639 | ||||||
chrX:54150447
|
C | T | 1 | a0001c0001t0056g0103 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.1158+798G>A | FAM120C | ENSG00000184083.12 | transcript | ENST00000375180.7 | protein_coding | 4/15 | chrX | 54150447 | ||||||
chrX:54150489
|
T | G | 2 | a0001c0001t0016g0139a0001c0001t0031g0138 | 2 | HG02486.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.1158+756A>C | FAM120C | ENSG00000184083.12 | transcript | ENST00000375180.7 | protein_coding | 4/15 | chrX | 54150489 | ||||||
chrX:54150984
|
G | T | 1 | a0001c0001t0026g0102 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.1158+261C>A | FAM120C | ENSG00000184083.12 | transcript | ENST00000375180.7 | protein_coding | 4/15 | chrX | 54150984 | ||||||
chrX:54151041
|
A | G | 1 | a0001c0001t0024g0080 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.1158+204T>C | FAM120C | ENSG00000184083.12 | transcript | ENST00000375180.7 | protein_coding | 4/15 | chrX | 54151041 | ||||||
chrX:54151157
|
G | T | 1 | a0001c0001t0001g0044 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.1158+88C>A | FAM120C | ENSG00000184083.12 | transcript | ENST00000375180.7 | protein_coding | 4/15 | chrX | 54151157 | ||||||
chrX:54151407
|
T | A | 1 | a0001c0001t0069g0074 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.1030-34A>T | FAM120C | ENSG00000184083.12 | transcript | ENST00000375180.7 | protein_coding | 3/15 | chrX | 54151407 | ||||||
chrX:54151416
|
G | T | 1 | a0001c0001t0061g0019 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.1030-43C>A | FAM120C | ENSG00000184083.12 | transcript | ENST00000375180.7 | protein_coding | 3/15 | chrX | 54151416 | ||||||
chrX:54151541
|
TTGGAAAA others(2): Show |
T | 2 | a0001c0001t0016g0139a0001c0001t0031g0138 | 2 | HG02486.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.1030-177_1030-169d others(11): Show |
FAM120C | ENSG00000184083.12 | transcript | ENST00000375180.7 | protein_coding | 3/15 | chrX | 54151541 | ||||||
chrX:54151560
|
A | G | 1 | a0002c0002t0047g0185 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.1030-187T>C | FAM120C | ENSG00000184083.12 | transcript | ENST00000375180.7 | protein_coding | 3/15 | chrX | 54151560 | ||||||
chrX:54151809
|
G | A | 3 | a0001c0001t0033g0012a0001c0001t0033g0013a0001c0001t0072g0106 | 3 | HG02559.hp2 HG02647.hp1 HG02809.hp1 |
intron_variant | MODIFIER | c.1030-436C>T | FAM120C | ENSG00000184083.12 | transcript | ENST00000375180.7 | protein_coding | 3/15 | chrX | 54151809 | ||||||
chrX:54151880
|
A | G | 6 | a0001c0001t0018g0115a0001c0001t0018g0116a0001c0001t0018g0151others(3): Show | 6 | HG02572.hp1 HG02615.hp2 HG02809.hp2 others(3): Show |
intron_variant | MODIFIER | c.1030-507T>C | FAM120C | ENSG00000184083.12 | transcript | ENST00000375180.7 | protein_coding | 3/15 | chrX | 54151880 | ||||||
chrX:54152021
|
A | AT | 7 | a0001c0001t0015g0015a0001c0001t0019g0120a0001c0001t0022g0016others(4): Show | 7 | HG00735.hp1 HG01243.hp1 HG01884.hp1 others(4): Show |
intron_variant | MODIFIER | c.1030-649dupA | FAM120C | ENSG00000184083.12 | transcript | ENST00000375180.7 | protein_coding | 3/15 | chrX | 54152021 | ||||||
chrX:54152054
|
G | A | 7 | a0001c0001t0002g0159a0001c0001t0002g0160a0001c0001t0002g0166others(4): Show | 7 | HG00621.hp1 HG02040.hp1 NA18950.hp1 others(4): Show |
intron_variant | MODIFIER | c.1030-681C>T | FAM120C | ENSG00000184083.12 | transcript | ENST00000375180.7 | protein_coding | 3/15 | chrX | 54152054 | ||||||
chrX:54152093
|
A | G | 3 | a0001c0001t0013g0130a0001c0001t0043g0147a0001c0001t0045g0148 | 3 | HG02896.hp2 HG02922.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.1030-720T>C | FAM120C | ENSG00000184083.12 | transcript | ENST00000375180.7 | protein_coding | 3/15 | chrX | 54152093 | ||||||
chrX:54152549
|
C | T | 1 | a0001c0001t0012g0043 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.1030-1176G>A | FAM120C | ENSG00000184083.12 | transcript | ENST00000375180.7 | protein_coding | 3/15 | chrX | 54152549 | ||||||
chrX:54152832
|
C | T | 177 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0022others(174): Show | 179 | HG00140.hp1 HG00280.hp1 HG00558.hp1 others(176): Show |
intron_variant | MODIFIER | c.1030-1459G>A | FAM120C | ENSG00000184083.12 | transcript | ENST00000375180.7 | protein_coding | 3/15 | chrX | 54152832 | ||||||
chrX:54153123
|
TA | T | 1 | a0001c0001t0002g0161 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.1030-1751delT | FAM120C | ENSG00000184083.12 | transcript | ENST00000375180.7 | protein_coding | 3/15 | chrX | 54153123 | ||||||
chrX:54153407
|
A | AT | 3 | a0001c0001t0033g0012a0001c0001t0033g0013a0001c0001t0072g0106 | 3 | HG02559.hp2 HG02647.hp1 HG02809.hp1 |
intron_variant | MODIFIER | c.1030-2035dupA | FAM120C | ENSG00000184083.12 | transcript | ENST00000375180.7 | protein_coding | 3/15 | chrX | 54153407 | ||||||
chrX:54153409
|
A | AT | 2 | a0001c0001t0015g0133a0001c0001t0031g0138 | 2 | HG02486.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.1030-2037dupA | FAM120C | ENSG00000184083.12 | transcript | ENST00000375180.7 | protein_coding | 3/15 | chrX | 54153409 | ||||||
chrX:54153409
|
A | T | 9 | a0001c0001t0018g0115a0001c0001t0018g0116a0001c0001t0018g0151others(6): Show | 9 | HG02559.hp2 HG02572.hp1 HG02615.hp2 others(6): Show |
intron_variant | MODIFIER | c.1030-2036T>A | FAM120C | ENSG00000184083.12 | transcript | ENST00000375180.7 | protein_coding | 3/15 | chrX | 54153409 | ||||||
chrX:54153409
|
AT | A | 1 | a0001c0001t0014g0075 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.1030-2037delA | FAM120C | ENSG00000184083.12 | transcript | ENST00000375180.7 | protein_coding | 3/15 | chrX | 54153409 | ||||||
chrX:54153411
|
T | A | 1 | a0001c0001t0014g0094 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.1030-2038A>T | FAM120C | ENSG00000184083.12 | transcript | ENST00000375180.7 | protein_coding | 3/15 | chrX | 54153411 | ||||||
chrX:54153550
|
G | C | 1 | a0001c0001t0039g0150 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.1030-2177C>G | FAM120C | ENSG00000184083.12 | transcript | ENST00000375180.7 | protein_coding | 3/15 | chrX | 54153550 | ||||||
chrX:54153573
|
A | AT | 3 | a0001c0001t0001g0008a0001c0001t0009g0033a0001c0001t0039g0150 | 3 | HG02738.hp1 NA18906.hp2 NA19079.hp1 |
intron_variant | MODIFIER | c.1030-2201dupA | FAM120C | ENSG00000184083.12 | transcript | ENST00000375180.7 | protein_coding | 3/15 | chrX | 54153573 | ||||||
chrX:54153573
|
AT | A | 1 | a0001c0001t0008g0170 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.1030-2201delA | FAM120C | ENSG00000184083.12 | transcript | ENST00000375180.7 | protein_coding | 3/15 | chrX | 54153573 | ||||||
chrX:54153851
|
C | A | 1 | a0001c0001t0019g0120 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.1030-2478G>T | FAM120C | ENSG00000184083.12 | transcript | ENST00000375180.7 | protein_coding | 3/15 | chrX | 54153851 | ||||||
chrX:54154037
|
G | GT | 5 | a0001c0001t0001g0025a0001c0001t0001g0177a0001c0001t0002g0153others(2): Show | 5 | NA18973.hp1 NA18973.hp2 NA18989.hp1 others(2): Show |
intron_variant | MODIFIER | c.1030-2665dupA | FAM120C | ENSG00000184083.12 | transcript | ENST00000375180.7 | protein_coding | 3/15 | chrX | 54154037 | ||||||
chrX:54154037
|
G | GTT | 1 | a0001c0001t0001g0042 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.1030-2666_1030-266 others(6): Show |
FAM120C | ENSG00000184083.12 | transcript | ENST00000375180.7 | protein_coding | 3/15 | chrX | 54154037 | ||||||
chrX:54154037
|
GT | G | 2 | a0001c0001t0025g0135a0001c0001t0066g0076 | 2 | HG02895.hp1 NA19089.hp1 |
intron_variant | MODIFIER | c.1030-2665delA | FAM120C | ENSG00000184083.12 | transcript | ENST00000375180.7 | protein_coding | 3/15 | chrX | 54154037 | ||||||
chrX:54154251
|
G | A | 1 | a0001c0001t0072g0106 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.1030-2878C>T | FAM120C | ENSG00000184083.12 | transcript | ENST00000375180.7 | protein_coding | 3/15 | chrX | 54154251 | ||||||
chrX:54154606
|
CA | C | 9 | a0001c0001t0003g0084a0001c0001t0004g0006a0001c0001t0021g0077others(6): Show | 9 | HG02074.hp1 HG02559.hp2 HG02615.hp1 others(6): Show |
intron_variant | MODIFIER | c.1029+3082delT | FAM120C | ENSG00000184083.12 | transcript | ENST00000375180.7 | protein_coding | 3/15 | chrX | 54154606 | ||||||
chrX:54154606
|
CAA | C | 173 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0022others(170): Show | 175 | HG00140.hp1 HG00280.hp1 HG00558.hp1 others(172): Show |
intron_variant | MODIFIER | c.1029+3081_1029+308 others(6): Show |
FAM120C | ENSG00000184083.12 | transcript | ENST00000375180.7 | protein_coding | 3/15 | chrX | 54154606 | ||||||
chrX:54154606
|
CAAA | C | 3 | a0001c0001t0002g0160a0001c0001t0015g0097a0001c0001t0018g0115 | 3 | HG02809.hp2 NA18957.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.1029+3080_1029+308 others(7): Show |
FAM120C | ENSG00000184083.12 | transcript | ENST00000375180.7 | protein_coding | 3/15 | chrX | 54154606 | ||||||
chrX:54154606
|
CAAAAAA | C | 1 | a0001c0001t0022g0119 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.1029+3077_1029+308 others(10): Show |
FAM120C | ENSG00000184083.12 | transcript | ENST00000375180.7 | protein_coding | 3/15 | chrX | 54154606 | ||||||
chrX:54155317
|
CAG | C | 1 | a0001c0001t0003g0084 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.1029+2370_1029+237 others(6): Show |
FAM120C | ENSG00000184083.12 | transcript | ENST00000375180.7 | protein_coding | 3/15 | chrX | 54155317 | ||||||
chrX:54155455
|
T | G | 1 | a0001c0001t0036g0078 | 1 | HG01169.hp2 | intron_variant | MODIFIER | c.1029+2234A>C | FAM120C | ENSG00000184083.12 | transcript | ENST00000375180.7 | protein_coding | 3/15 | chrX | 54155455 | ||||||
chrX:54155662
|
TTA | T | 1 | a0001c0001t0008g0170 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.1029+2025_1029+202 others(6): Show |
FAM120C | ENSG00000184083.12 | transcript | ENST00000375180.7 | protein_coding | 3/15 | chrX | 54155662 | ||||||
chrX:54155663
|
TA | T | 186 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0022others(183): Show | 188 | HG00140.hp1 HG00280.hp1 HG00558.hp1 others(185): Show |
intron_variant | MODIFIER | c.1029+2025delT | FAM120C | ENSG00000184083.12 | transcript | ENST00000375180.7 | protein_coding | 3/15 | chrX | 54155663 | ||||||
chrX:54155699
|
G | A | 2 | a0001c0001t0033g0012a0001c0001t0033g0013 | 2 | HG02559.hp2 HG02647.hp1 |
intron_variant | MODIFIER | c.1029+1990C>T | FAM120C | ENSG00000184083.12 | transcript | ENST00000375180.7 | protein_coding | 3/15 | chrX | 54155699 | ||||||
chrX:54155936
|
A | T | 8 | a0001c0001t0003g0040a0001c0001t0003g0041a0001c0001t0012g0127others(5): Show | 8 | HG02630.hp2 HG02895.hp1 HG02896.hp1 others(5): Show |
intron_variant | MODIFIER | c.1029+1753T>A | FAM120C | ENSG00000184083.12 | transcript | ENST00000375180.7 | protein_coding | 3/15 | chrX | 54155936 | ||||||
chrX:54156219
|
A | G | 1 | a0002c0002t0007g0184 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.1029+1470T>C | FAM120C | ENSG00000184083.12 | transcript | ENST00000375180.7 | protein_coding | 3/15 | chrX | 54156219 | ||||||
chrX:54156315
|
CT | C | 165 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0022others(162): Show | 167 | HG00140.hp1 HG00280.hp1 HG00558.hp1 others(164): Show |
intron_variant | MODIFIER | c.1029+1373delA | FAM120C | ENSG00000184083.12 | transcript | ENST00000375180.7 | protein_coding | 3/15 | chrX | 54156315 | ||||||
chrX:54156315
|
CTT | C | 2 | a0001c0001t0001g0079a0001c0001t0003g0110 | 2 | HG01433.hp1 NA19005.hp1 |
intron_variant | MODIFIER | c.1029+1372_1029+137 others(6): Show |
FAM120C | ENSG00000184083.12 | transcript | ENST00000375180.7 | protein_coding | 3/15 | chrX | 54156315 | ||||||
chrX:54156697
|
G | A | 3 | a0001c0001t0033g0012a0001c0001t0033g0013a0001c0001t0072g0106 | 3 | HG02559.hp2 HG02647.hp1 HG02809.hp1 |
intron_variant | MODIFIER | c.1029+992C>T | FAM120C | ENSG00000184083.12 | transcript | ENST00000375180.7 | protein_coding | 3/15 | chrX | 54156697 | ||||||
chrX:54156886
|
C | CA | 23 | a0001c0001t0001g0022a0001c0001t0002g0153a0001c0001t0007g0081others(20): Show | 23 | HG00673.hp1 HG01255.hp1 HG02027.hp1 others(20): Show |
intron_variant | MODIFIER | c.1029+802dupT | FAM120C | ENSG00000184083.12 | transcript | ENST00000375180.7 | protein_coding | 3/15 | chrX | 54156886 | ||||||
chrX:54156886
|
C | CAA | 1 | a0001c0001t0003g0181 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.1029+801_1029+802d others(4): Show |
FAM120C | ENSG00000184083.12 | transcript | ENST00000375180.7 | protein_coding | 3/15 | chrX | 54156886 | ||||||
chrX:54156886
|
CA | C | 5 | a0001c0001t0002g0159a0001c0001t0016g0137a0001c0001t0017g0005others(2): Show | 5 | HG01169.hp1 HG02040.hp1 HG02451.hp2 others(2): Show |
intron_variant | MODIFIER | c.1029+802delT | FAM120C | ENSG00000184083.12 | transcript | ENST00000375180.7 | protein_coding | 3/15 | chrX | 54156886 | ||||||
chrX:54156886
|
CAA | C | 1 | a0001c0001t0017g0171 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.1029+801_1029+802d others(4): Show |
FAM120C | ENSG00000184083.12 | transcript | ENST00000375180.7 | protein_coding | 3/15 | chrX | 54156886 | ||||||
chrX:54156918
|
G | C | 1 | a0001c0001t0043g0147 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.1029+771C>G | FAM120C | ENSG00000184083.12 | transcript | ENST00000375180.7 | protein_coding | 3/15 | chrX | 54156918 | ||||||
chrX:54157004
|
G | A | 6 | a0001c0001t0018g0115a0001c0001t0018g0116a0001c0001t0018g0151others(3): Show | 6 | HG02572.hp1 HG02615.hp2 HG02809.hp2 others(3): Show |
intron_variant | MODIFIER | c.1029+685C>T | FAM120C | ENSG00000184083.12 | transcript | ENST00000375180.7 | protein_coding | 3/15 | chrX | 54157004 | ||||||
chrX:54157130
|
C | A | 5 | a0001c0001t0015g0133a0001c0001t0015g0136a0001c0001t0025g0135others(2): Show | 5 | HG02630.hp2 HG02895.hp1 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.1029+559G>T | FAM120C | ENSG00000184083.12 | transcript | ENST00000375180.7 | protein_coding | 3/15 | chrX | 54157130 | ||||||
chrX:54157415
|
C | T | 1 | a0001c0001t0042g0183 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.1029+274G>A | FAM120C | ENSG00000184083.12 | transcript | ENST00000375180.7 | protein_coding | 3/15 | chrX | 54157415 | ||||||
chrX:54158042
|
T | G | 2 | a0001c0001t0027g0117a0001c0001t0027g0118 | 2 | HG06807.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.947-271A>C | FAM120C | ENSG00000184083.12 | transcript | ENST00000375180.7 | protein_coding | 2/15 | chrX | 54158042 | ||||||
chrX:54158314
|
A | G | 1 | a0001c0001t0067g0018 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.947-543T>C | FAM120C | ENSG00000184083.12 | transcript | ENST00000375180.7 | protein_coding | 2/15 | chrX | 54158314 | ||||||
chrX:54158693
|
T | C | 9 | a0001c0001t0018g0115a0001c0001t0018g0116a0001c0001t0018g0151others(6): Show | 9 | HG02559.hp2 HG02572.hp1 HG02615.hp2 others(6): Show |
intron_variant | MODIFIER | c.946+677A>G | FAM120C | ENSG00000184083.12 | transcript | ENST00000375180.7 | protein_coding | 2/15 | chrX | 54158693 | ||||||
chrX:54159102
|
T | A | 1 | a0001c0001t0033g0013 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.946+268A>T | FAM120C | ENSG00000184083.12 | transcript | ENST00000375180.7 | protein_coding | 2/15 | chrX | 54159102 | ||||||
chrX:54159257
|
A | C | 6 | a0001c0001t0018g0115a0001c0001t0018g0116a0001c0001t0018g0151others(3): Show | 6 | HG02572.hp1 HG02615.hp2 HG02809.hp2 others(3): Show |
intron_variant | MODIFIER | c.946+113T>G | FAM120C | ENSG00000184083.12 | transcript | ENST00000375180.7 | protein_coding | 2/15 | chrX | 54159257 | ||||||
chrX:54159258
|
G | C | 6 | a0001c0001t0018g0115a0001c0001t0018g0116a0001c0001t0018g0151others(3): Show | 6 | HG02572.hp1 HG02615.hp2 HG02809.hp2 others(3): Show |
intron_variant | MODIFIER | c.946+112C>G | FAM120C | ENSG00000184083.12 | transcript | ENST00000375180.7 | protein_coding | 2/15 | chrX | 54159258 | ||||||
chrX:54159692
|
T | C | 3 | a0001c0001t0012g0104a0001c0001t0062g0182a0001c0001t0065g0083 | 3 | HG02083.hp1 HG02135.hp1 NA19067.hp1 |
intron_variant | MODIFIER | c.700-76A>G | FAM120C | ENSG00000184083.12 | transcript | ENST00000375180.7 | protein_coding | 1/15 | chrX | 54159692 | ||||||
chrX:54159761
|
C | CT | 4 | a0001c0001t0008g0158a0001c0001t0033g0012a0001c0001t0033g0013others(1): Show | 4 | HG00621.hp1 HG02559.hp2 HG02647.hp1 others(1): Show |
intron_variant | MODIFIER | c.700-146dupA | FAM120C | ENSG00000184083.12 | transcript | ENST00000375180.7 | protein_coding | 1/15 | chrX | 54159761 | ||||||
chrX:54159761
|
CT | C | 3 | a0001c0001t0006g0026a0001c0001t0015g0136a0001c0001t0018g0116 | 3 | HG02896.hp1 HG06807.hp1 NA18955.hp1 |
intron_variant | MODIFIER | c.700-146delA | FAM120C | ENSG00000184083.12 | transcript | ENST00000375180.7 | protein_coding | 1/15 | chrX | 54159761 | ||||||
chrX:54160171
|
T | C | 1 | a0001c0001t0017g0171 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.700-555A>G | FAM120C | ENSG00000184083.12 | transcript | ENST00000375180.7 | protein_coding | 1/15 | chrX | 54160171 | ||||||
chrX:54160220
|
C | G | 10 | a0001c0001t0016g0137a0001c0001t0016g0139a0001c0001t0016g0141others(7): Show | 10 | HG01255.hp1 HG01884.hp2 HG02055.hp1 others(7): Show |
intron_variant | MODIFIER | c.700-604G>C | FAM120C | ENSG00000184083.12 | transcript | ENST00000375180.7 | protein_coding | 1/15 | chrX | 54160220 | ||||||
chrX:54160493
|
C | T | 1 | a0001c0001t0003g0032 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.700-877G>A | FAM120C | ENSG00000184083.12 | transcript | ENST00000375180.7 | protein_coding | 1/15 | chrX | 54160493 | ||||||
chrX:54160757
|
C | A | 1 | a0001c0001t0018g0151 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.700-1141G>T | FAM120C | ENSG00000184083.12 | transcript | ENST00000375180.7 | protein_coding | 1/15 | chrX | 54160757 | ||||||
chrX:54160806
|
G | A | 1 | a0001c0001t0001g0025 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.700-1190C>T | FAM120C | ENSG00000184083.12 | transcript | ENST00000375180.7 | protein_coding | 1/15 | chrX | 54160806 | ||||||
chrX:54161287
|
C | T | 1 | a0001c0001t0015g0133 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.700-1671G>A | FAM120C | ENSG00000184083.12 | transcript | ENST00000375180.7 | protein_coding | 1/15 | chrX | 54161287 | ||||||
chrX:54161405
|
C | T | 10 | a0001c0001t0016g0137a0001c0001t0016g0139a0001c0001t0016g0141others(7): Show | 10 | HG01255.hp1 HG01884.hp2 HG02055.hp1 others(7): Show |
intron_variant | MODIFIER | c.700-1789G>A | FAM120C | ENSG00000184083.12 | transcript | ENST00000375180.7 | protein_coding | 1/15 | chrX | 54161405 | ||||||
chrX:54162263
|
A | G | 1 | a0001c0001t0021g0014 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.700-2647T>C | FAM120C | ENSG00000184083.12 | transcript | ENST00000375180.7 | protein_coding | 1/15 | chrX | 54162263 | ||||||
chrX:54162434
|
GAC | G | 1 | a0001c0009t0071g0031 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.700-2820_700-2819d others(4): Show |
FAM120C | ENSG00000184083.12 | transcript | ENST00000375180.7 | protein_coding | 1/15 | chrX | 54162434 | ||||||
chrX:54162707
|
C | T | 3 | a0001c0001t0006g0028a0001c0001t0006g0029a0001c0001t0006g0030 | 3 | NA18990.hp1 NA19085.hp1 NA19088.hp1 |
intron_variant | MODIFIER | c.700-3091G>A | FAM120C | ENSG00000184083.12 | transcript | ENST00000375180.7 | protein_coding | 1/15 | chrX | 54162707 | ||||||
chrX:54162943
|
T | C | 6 | a0001c0001t0015g0133a0001c0001t0015g0136a0001c0001t0022g0149others(3): Show | 6 | HG02630.hp2 HG02895.hp1 HG02896.hp1 others(3): Show |
intron_variant | MODIFIER | c.700-3327A>G | FAM120C | ENSG00000184083.12 | transcript | ENST00000375180.7 | protein_coding | 1/15 | chrX | 54162943 | ||||||
chrX:54163250
|
G | T | 3 | a0001c0001t0033g0012a0001c0001t0033g0013a0001c0001t0072g0106 | 3 | HG02559.hp2 HG02647.hp1 HG02809.hp1 |
intron_variant | MODIFIER | c.700-3634C>A | FAM120C | ENSG00000184083.12 | transcript | ENST00000375180.7 | protein_coding | 1/15 | chrX | 54163250 | ||||||
chrX:54163251
|
C | G | 3 | a0001c0001t0033g0012a0001c0001t0033g0013a0001c0001t0072g0106 | 3 | HG02559.hp2 HG02647.hp1 HG02809.hp1 |
intron_variant | MODIFIER | c.700-3635G>C | FAM120C | ENSG00000184083.12 | transcript | ENST00000375180.7 | protein_coding | 1/15 | chrX | 54163251 | ||||||
chrX:54163467
|
G | C | 1 | a0001c0001t0018g0116 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.700-3851C>G | FAM120C | ENSG00000184083.12 | transcript | ENST00000375180.7 | protein_coding | 1/15 | chrX | 54163467 | ||||||
chrX:54163487
|
A | T | 7 | a0001c0001t0001g0177a0001c0001t0002g0153a0001c0001t0002g0174others(4): Show | 7 | HG00558.hp2 HG00609.hp1 NA18966.hp1 others(4): Show |
intron_variant | MODIFIER | c.700-3871T>A | FAM120C | ENSG00000184083.12 | transcript | ENST00000375180.7 | protein_coding | 1/15 | chrX | 54163487 | ||||||
chrX:54163556
|
T | G | 3 | a0001c0001t0033g0012a0001c0001t0033g0013a0001c0001t0072g0106 | 3 | HG02559.hp2 HG02647.hp1 HG02809.hp1 |
intron_variant | MODIFIER | c.700-3940A>C | FAM120C | ENSG00000184083.12 | transcript | ENST00000375180.7 | protein_coding | 1/15 | chrX | 54163556 | ||||||
chrX:54163673
|
C | T | 3 | a0001c0001t0033g0012a0001c0001t0033g0013a0001c0001t0072g0106 | 3 | HG02559.hp2 HG02647.hp1 HG02809.hp1 |
intron_variant | MODIFIER | c.700-4057G>A | FAM120C | ENSG00000184083.12 | transcript | ENST00000375180.7 | protein_coding | 1/15 | chrX | 54163673 | ||||||
chrX:54163682
|
TA | T | 1 | a0001c0001t0032g0178 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.700-4067delT | FAM120C | ENSG00000184083.12 | transcript | ENST00000375180.7 | protein_coding | 1/15 | chrX | 54163682 | ||||||
chrX:54163884
|
T | TTG | 1 | a0001c0001t0003g0084 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.700-4270_700-4269d others(4): Show |
FAM120C | ENSG00000184083.12 | transcript | ENST00000375180.7 | protein_coding | 1/15 | chrX | 54163884 | ||||||
chrX:54163884
|
TTG | T | 2 | a0001c0001t0033g0012a0001c0001t0067g0018 | 2 | HG02257.hp1 HG02559.hp2 |
intron_variant | MODIFIER | c.700-4270_700-4269d others(4): Show |
FAM120C | ENSG00000184083.12 | transcript | ENST00000375180.7 | protein_coding | 1/15 | chrX | 54163884 | ||||||
chrX:54163884
|
TTGTG | T | 78 | a0001c0001t0001g0177a0001c0001t0002g0132a0001c0001t0002g0153others(75): Show | 79 | HG00558.hp2 HG00609.hp1 HG00621.hp1 others(76): Show |
intron_variant | MODIFIER | c.700-4272_700-4269d others(6): Show |
FAM120C | ENSG00000184083.12 | transcript | ENST00000375180.7 | protein_coding | 1/15 | chrX | 54163884 | ||||||
chrX:54163938
|
A | AT | 1 | a0001c0001t0013g0130 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.700-4323dupA | FAM120C | ENSG00000184083.12 | transcript | ENST00000375180.7 | protein_coding | 1/15 | chrX | 54163938 | ||||||
chrX:54163938
|
A | T | 8 | a0001c0001t0001g0027a0001c0001t0027g0117a0001c0001t0027g0118others(5): Show | 8 | HG02559.hp2 HG02647.hp1 HG02698.hp1 others(5): Show |
intron_variant | MODIFIER | c.700-4322T>A | FAM120C | ENSG00000184083.12 | transcript | ENST00000375180.7 | protein_coding | 1/15 | chrX | 54163938 | ||||||
chrX:54163938
|
AT | A | 2 | a0001c0001t0006g0026a0001c0001t0013g0112 | 2 | HG02630.hp1 NA18955.hp1 |
intron_variant | MODIFIER | c.700-4323delA | FAM120C | ENSG00000184083.12 | transcript | ENST00000375180.7 | protein_coding | 1/15 | chrX | 54163938 | ||||||
chrX:54163939
|
T | TA | 2 | a0001c0001t0003g0087a0001c0001t0003g0110 | 2 | HG01433.hp1 HG02300.hp1 |
intron_variant | MODIFIER | c.700-4324_700-4323i others(3): Show |
FAM120C | ENSG00000184083.12 | transcript | ENST00000375180.7 | protein_coding | 1/15 | chrX | 54163939 | ||||||
chrX:54163940
|
T | A | 3 | a0001c0001t0004g0086a0001c0001t0026g0102a0001c0001t0046g0085 | 3 | HG01928.hp1 HG02129.hp1 HG02145.hp1 |
intron_variant | MODIFIER | c.700-4324A>T | FAM120C | ENSG00000184083.12 | transcript | ENST00000375180.7 | protein_coding | 1/15 | chrX | 54163940 | ||||||
chrX:54164035
|
C | T | 9 | a0001c0001t0016g0137a0001c0001t0016g0139a0001c0001t0016g0141others(6): Show | 9 | HG01255.hp1 HG01884.hp2 HG02055.hp1 others(6): Show |
intron_variant | MODIFIER | c.700-4419G>A | FAM120C | ENSG00000184083.12 | transcript | ENST00000375180.7 | protein_coding | 1/15 | chrX | 54164035 | ||||||
chrX:54164250
|
A | AT | 1 | a0001c0001t0032g0178 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.700-4635dupA | FAM120C | ENSG00000184083.12 | transcript | ENST00000375180.7 | protein_coding | 1/15 | chrX | 54164250 | ||||||
chrX:54164465
|
G | A | 2 | a0001c0001t0003g0087a0001c0001t0003g0110 | 2 | HG01433.hp1 HG02300.hp1 |
intron_variant | MODIFIER | c.700-4849C>T | FAM120C | ENSG00000184083.12 | transcript | ENST00000375180.7 | protein_coding | 1/15 | chrX | 54164465 | ||||||
chrX:54164497
|
G | A | 1 | a0001c0001t0002g0172 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.700-4881C>T | FAM120C | ENSG00000184083.12 | transcript | ENST00000375180.7 | protein_coding | 1/15 | chrX | 54164497 | ||||||
chrX:54164611
|
A | G | 1 | a0001c0001t0015g0097 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.700-4995T>C | FAM120C | ENSG00000184083.12 | transcript | ENST00000375180.7 | protein_coding | 1/15 | chrX | 54164611 | ||||||
chrX:54164632
|
T | C | 1 | a0001c0001t0072g0106 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.700-5016A>G | FAM120C | ENSG00000184083.12 | transcript | ENST00000375180.7 | protein_coding | 1/15 | chrX | 54164632 | ||||||
chrX:54164817
|
A | T | 10 | a0001c0001t0018g0115a0001c0001t0018g0116a0001c0001t0018g0151others(7): Show | 10 | HG02559.hp2 HG02572.hp1 HG02615.hp2 others(7): Show |
intron_variant | MODIFIER | c.700-5201T>A | FAM120C | ENSG00000184083.12 | transcript | ENST00000375180.7 | protein_coding | 1/15 | chrX | 54164817 | ||||||
chrX:54164919
|
A | AT | 1 | a0001c0001t0006g0026 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.700-5304dupA | FAM120C | ENSG00000184083.12 | transcript | ENST00000375180.7 | protein_coding | 1/15 | chrX | 54164919 | ||||||
chrX:54164925
|
T | G | 1 | a0001c0001t0029g0088 | 1 | HG03492.hp1 | intron_variant | MODIFIER | c.700-5309A>C | FAM120C | ENSG00000184083.12 | transcript | ENST00000375180.7 | protein_coding | 1/15 | chrX | 54164925 | ||||||
chrX:54164931
|
G | GT | 1 | a0001c0001t0005g0113 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.700-5316dupA | FAM120C | ENSG00000184083.12 | transcript | ENST00000375180.7 | protein_coding | 1/15 | chrX | 54164931 | ||||||
chrX:54164952
|
C | A | 2 | a0002c0002t0019g0186a0002c0002t0047g0185 | 2 | HG00642.hp1 HG00735.hp2 |
intron_variant | MODIFIER | c.700-5336G>T | FAM120C | ENSG00000184083.12 | transcript | ENST00000375180.7 | protein_coding | 1/15 | chrX | 54164952 | ||||||
chrX:54165255
|
G | A | 1 | a0001c0001t0033g0013 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.700-5639C>T | FAM120C | ENSG00000184083.12 | transcript | ENST00000375180.7 | protein_coding | 1/15 | chrX | 54165255 | ||||||
chrX:54165594
|
T | TG | 1 | a0001c0001t0032g0178 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.700-5979dupC | FAM120C | ENSG00000184083.12 | transcript | ENST00000375180.7 | protein_coding | 1/15 | chrX | 54165594 | ||||||
chrX:54165776
|
C | CA | 1 | a0001c0001t0010g0023 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.700-6161dupT | FAM120C | ENSG00000184083.12 | transcript | ENST00000375180.7 | protein_coding | 1/15 | chrX | 54165776 | ||||||
chrX:54165800
|
T | TA | 3 | a0001c0001t0013g0130a0003c0003t0013g0121a0003c0003t0013g0122 | 3 | HG02896.hp2 HG03098.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.700-6185dupT | FAM120C | ENSG00000184083.12 | transcript | ENST00000375180.7 | protein_coding | 1/15 | chrX | 54165800 | ||||||
chrX:54166001
|
T | A | 1 | a0001c0001t0033g0013 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.700-6385A>T | FAM120C | ENSG00000184083.12 | transcript | ENST00000375180.7 | protein_coding | 1/15 | chrX | 54166001 | ||||||
chrX:54166087
|
GA | G | 1 | a0001c0001t0032g0178 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.700-6472delT | FAM120C | ENSG00000184083.12 | transcript | ENST00000375180.7 | protein_coding | 1/15 | chrX | 54166087 | ||||||
chrX:54166379
|
G | C | 1 | a0001c0001t0049g0152 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.700-6763C>G | FAM120C | ENSG00000184083.12 | transcript | ENST00000375180.7 | protein_coding | 1/15 | chrX | 54166379 | ||||||
chrX:54166413
|
C | A | 1 | a0001c0001t0023g0089 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.700-6797G>T | FAM120C | ENSG00000184083.12 | transcript | ENST00000375180.7 | protein_coding | 1/15 | chrX | 54166413 | ||||||
chrX:54166611
|
C | T | 10 | a0001c0001t0016g0137a0001c0001t0016g0139a0001c0001t0016g0141others(7): Show | 10 | HG01255.hp1 HG01884.hp2 HG02055.hp1 others(7): Show |
intron_variant | MODIFIER | c.700-6995G>A | FAM120C | ENSG00000184083.12 | transcript | ENST00000375180.7 | protein_coding | 1/15 | chrX | 54166611 | ||||||
chrX:54166656
|
A | G | 1 | a0001c0001t0001g0001 | 2 | HG01257.hp1 HG01258.hp1 |
intron_variant | MODIFIER | c.700-7040T>C | FAM120C | ENSG00000184083.12 | transcript | ENST00000375180.7 | protein_coding | 1/15 | chrX | 54166656 | ||||||
chrX:54166680
|
GT | G | 1 | a0001c0001t0032g0178 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.700-7065delA | FAM120C | ENSG00000184083.12 | transcript | ENST00000375180.7 | protein_coding | 1/15 | chrX | 54166680 | ||||||
chrX:54166952
|
A | G | 1 | a0001c0001t0067g0018 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.700-7336T>C | FAM120C | ENSG00000184083.12 | transcript | ENST00000375180.7 | protein_coding | 1/15 | chrX | 54166952 | ||||||
chrX:54167108
|
C | T | 6 | a0001c0001t0018g0115a0001c0001t0018g0116a0001c0001t0018g0151others(3): Show | 6 | HG02572.hp1 HG02615.hp2 HG02809.hp2 others(3): Show |
intron_variant | MODIFIER | c.700-7492G>A | FAM120C | ENSG00000184083.12 | transcript | ENST00000375180.7 | protein_coding | 1/15 | chrX | 54167108 | ||||||
chrX:54167470
|
T | G | 1 | a0001c0001t0063g0009 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.700-7854A>C | FAM120C | ENSG00000184083.12 | transcript | ENST00000375180.7 | protein_coding | 1/15 | chrX | 54167470 | ||||||
chrX:54167519
|
AG | A | 1 | a0001c0001t0010g0023 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.700-7904delC | FAM120C | ENSG00000184083.12 | transcript | ENST00000375180.7 | protein_coding | 1/15 | chrX | 54167519 | ||||||
chrX:54167740
|
G | A | 1 | a0001c0001t0012g0104 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.700-8124C>T | FAM120C | ENSG00000184083.12 | transcript | ENST00000375180.7 | protein_coding | 1/15 | chrX | 54167740 | ||||||
chrX:54167800
|
AT | A | 10 | a0001c0001t0016g0137a0001c0001t0016g0139a0001c0001t0016g0141others(7): Show | 10 | HG01255.hp1 HG01884.hp2 HG02055.hp1 others(7): Show |
intron_variant | MODIFIER | c.700-8185delA | FAM120C | ENSG00000184083.12 | transcript | ENST00000375180.7 | protein_coding | 1/15 | chrX | 54167800 | ||||||
chrX:54167803
|
T | TA | 1 | a0001c0001t0001g0022 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.700-8188dupT | FAM120C | ENSG00000184083.12 | transcript | ENST00000375180.7 | protein_coding | 1/15 | chrX | 54167803 | ||||||
chrX:54167803
|
TA | T | 69 | a0001c0001t0001g0025a0001c0001t0001g0177a0001c0001t0002g0132others(66): Show | 70 | HG00558.hp2 HG00609.hp1 HG00621.hp1 others(67): Show |
intron_variant | MODIFIER | c.700-8188delT | FAM120C | ENSG00000184083.12 | transcript | ENST00000375180.7 | protein_coding | 1/15 | chrX | 54167803 | ||||||
chrX:54167805
|
A | T | 28 | a0001c0001t0001g0177a0001c0001t0002g0153a0001c0001t0002g0159others(25): Show | 29 | HG00558.hp2 HG00609.hp1 HG00621.hp1 others(26): Show |
intron_variant | MODIFIER | c.700-8189T>A | FAM120C | ENSG00000184083.12 | transcript | ENST00000375180.7 | protein_coding | 1/15 | chrX | 54167805 | ||||||
chrX:54167851
|
C | G | 1 | a0001c0001t0059g0024 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.700-8235G>C | FAM120C | ENSG00000184083.12 | transcript | ENST00000375180.7 | protein_coding | 1/15 | chrX | 54167851 | ||||||
chrX:54167967
|
C | CA | 5 | a0001c0001t0005g0095a0001c0001t0013g0112a0001c0001t0019g0111others(2): Show | 5 | HG02559.hp2 HG02630.hp1 HG02809.hp1 others(2): Show |
intron_variant | MODIFIER | c.700-8352dupT | FAM120C | ENSG00000184083.12 | transcript | ENST00000375180.7 | protein_coding | 1/15 | chrX | 54167967 | ||||||
chrX:54167967
|
C | CAA | 1 | a0001c0001t0033g0013 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.700-8353_700-8352d others(4): Show |
FAM120C | ENSG00000184083.12 | transcript | ENST00000375180.7 | protein_coding | 1/15 | chrX | 54167967 | ||||||
chrX:54167967
|
CA | C | 4 | a0001c0001t0011g0155a0001c0001t0058g0020a0001c0001t0061g0019others(1): Show | 4 | HG01069.hp1 HG01952.hp1 HG02132.hp1 others(1): Show |
intron_variant | MODIFIER | c.700-8352delT | FAM120C | ENSG00000184083.12 | transcript | ENST00000375180.7 | protein_coding | 1/15 | chrX | 54167967 | ||||||
chrX:54168037
|
T | C | 9 | a0001c0001t0018g0115a0001c0001t0018g0116a0001c0001t0018g0151others(6): Show | 9 | HG02559.hp2 HG02572.hp1 HG02615.hp2 others(6): Show |
intron_variant | MODIFIER | c.700-8421A>G | FAM120C | ENSG00000184083.12 | transcript | ENST00000375180.7 | protein_coding | 1/15 | chrX | 54168037 | ||||||
chrX:54168103
|
C | T | 3 | a0001c0001t0033g0012a0001c0001t0033g0013a0001c0001t0072g0106 | 3 | HG02559.hp2 HG02647.hp1 HG02809.hp1 |
intron_variant | MODIFIER | c.700-8487G>A | FAM120C | ENSG00000184083.12 | transcript | ENST00000375180.7 | protein_coding | 1/15 | chrX | 54168103 | ||||||
chrX:54168394
|
CA | C | 1 | a0001c0001t0010g0023 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.700-8779delT | FAM120C | ENSG00000184083.12 | transcript | ENST00000375180.7 | protein_coding | 1/15 | chrX | 54168394 | ||||||
chrX:54168591
|
T | A | 1 | a0001c0001t0038g0090 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.700-8975A>T | FAM120C | ENSG00000184083.12 | transcript | ENST00000375180.7 | protein_coding | 1/15 | chrX | 54168591 | ||||||
chrX:54168882
|
T | C | 1 | a0001c0001t0010g0175 | 1 | NA18980.hp2 | intron_variant | MODIFIER | c.700-9266A>G | FAM120C | ENSG00000184083.12 | transcript | ENST00000375180.7 | protein_coding | 1/15 | chrX | 54168882 | ||||||
chrX:54169235
|
C | A | 3 | a0001c0001t0033g0012a0001c0001t0033g0013a0001c0001t0072g0106 | 3 | HG02559.hp2 HG02647.hp1 HG02809.hp1 |
intron_variant | MODIFIER | c.700-9619G>T | FAM120C | ENSG00000184083.12 | transcript | ENST00000375180.7 | protein_coding | 1/15 | chrX | 54169235 | ||||||
chrX:54169329
|
T | C | 1 | a0008c0010t0075g0188 | 1 | NA19055.hp1 | intron_variant | MODIFIER | c.700-9713A>G | FAM120C | ENSG00000184083.12 | transcript | ENST00000375180.7 | protein_coding | 1/15 | chrX | 54169329 | ||||||
chrX:54169421
|
C | G | 1 | a0001c0001t0004g0180 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.700-9805G>C | FAM120C | ENSG00000184083.12 | transcript | ENST00000375180.7 | protein_coding | 1/15 | chrX | 54169421 | ||||||
chrX:54169535
|
G | A | 3 | a0001c0001t0033g0012a0001c0001t0033g0013a0001c0001t0072g0106 | 3 | HG02559.hp2 HG02647.hp1 HG02809.hp1 |
intron_variant | MODIFIER | c.700-9919C>T | FAM120C | ENSG00000184083.12 | transcript | ENST00000375180.7 | protein_coding | 1/15 | chrX | 54169535 | ||||||
chrX:54169611
|
C | T | 1 | a0001c0001t0001g0022 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.700-9995G>A | FAM120C | ENSG00000184083.12 | transcript | ENST00000375180.7 | protein_coding | 1/15 | chrX | 54169611 | ||||||
chrX:54169871
|
C | A | 1 | a0001c0001t0019g0120 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.700-10255G>T | FAM120C | ENSG00000184083.12 | transcript | ENST00000375180.7 | protein_coding | 1/15 | chrX | 54169871 | ||||||
chrX:54170722
|
C | CGTAA | 2 | a0001c0001t0010g0091a0001c0001t0010g0092 | 2 | NA18612.hp1 NA18967.hp1 |
intron_variant | MODIFIER | c.700-11107_700-1110 others(8): Show |
FAM120C | ENSG00000184083.12 | transcript | ENST00000375180.7 | protein_coding | 1/15 | chrX | 54170722 | ||||||
chrX:54170814
|
C | T | 9 | a0001c0001t0018g0115a0001c0001t0018g0116a0001c0001t0018g0151others(6): Show | 9 | HG02559.hp2 HG02572.hp1 HG02615.hp2 others(6): Show |
intron_variant | MODIFIER | c.700-11198G>A | FAM120C | ENSG00000184083.12 | transcript | ENST00000375180.7 | protein_coding | 1/15 | chrX | 54170814 | ||||||
chrX:54170951
|
G | A | 2 | a0001c0001t0014g0093a0001c0001t0014g0094 | 2 | HG02602.hp1 HG02735.hp1 |
intron_variant | MODIFIER | c.700-11335C>T | FAM120C | ENSG00000184083.12 | transcript | ENST00000375180.7 | protein_coding | 1/15 | chrX | 54170951 | ||||||
chrX:54170983
|
G | A | 2 | a0001c0001t0005g0011a0001c0001t0011g0010 | 2 | NA18980.hp1 NA19077.hp2 |
intron_variant | MODIFIER | c.700-11367C>T | FAM120C | ENSG00000184083.12 | transcript | ENST00000375180.7 | protein_coding | 1/15 | chrX | 54170983 | ||||||
chrX:54171021
|
A | AAG | 9 | a0001c0001t0018g0115a0001c0001t0018g0116a0001c0001t0018g0151others(6): Show | 9 | HG02559.hp2 HG02572.hp1 HG02615.hp2 others(6): Show |
intron_variant | MODIFIER | c.700-11407_700-1140 others(6): Show |
FAM120C | ENSG00000184083.12 | transcript | ENST00000375180.7 | protein_coding | 1/15 | chrX | 54171021 | ||||||
chrX:54171289
|
T | C | 1 | a0001c0001t0002g0174 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.699+11211A>G | FAM120C | ENSG00000184083.12 | transcript | ENST00000375180.7 | protein_coding | 1/15 | chrX | 54171289 | ||||||
chrX:54171407
|
TA | T | 1 | a0008c0010t0075g0188 | 1 | NA19055.hp1 | intron_variant | MODIFIER | c.699+11092delT | FAM120C | ENSG00000184083.12 | transcript | ENST00000375180.7 | protein_coding | 1/15 | chrX | 54171407 | ||||||
chrX:54171885
|
G | A | 68 | a0001c0001t0001g0177a0001c0001t0002g0132a0001c0001t0002g0153others(65): Show | 69 | HG00558.hp2 HG00609.hp1 HG00621.hp1 others(66): Show |
intron_variant | MODIFIER | c.699+10615C>T | FAM120C | ENSG00000184083.12 | transcript | ENST00000375180.7 | protein_coding | 1/15 | chrX | 54171885 | ||||||
chrX:54172269
|
T | C | 64 | a0001c0001t0001g0177a0001c0001t0002g0132a0001c0001t0002g0153others(61): Show | 65 | HG00558.hp2 HG00609.hp1 HG00621.hp1 others(62): Show |
intron_variant | MODIFIER | c.699+10231A>G | FAM120C | ENSG00000184083.12 | transcript | ENST00000375180.7 | protein_coding | 1/15 | chrX | 54172269 | ||||||
chrX:54172653
|
A | T | 3 | a0001c0001t0033g0012a0001c0001t0033g0013a0001c0001t0072g0106 | 3 | HG02559.hp2 HG02647.hp1 HG02809.hp1 |
intron_variant | MODIFIER | c.699+9847T>A | FAM120C | ENSG00000184083.12 | transcript | ENST00000375180.7 | protein_coding | 1/15 | chrX | 54172653 | ||||||
chrX:54173237
|
A | AT | 1 | a0001c0001t0017g0005 | 1 | HG01169.hp1 | intron_variant | MODIFIER | c.699+9262dupA | FAM120C | ENSG00000184083.12 | transcript | ENST00000375180.7 | protein_coding | 1/15 | chrX | 54173237 | ||||||
chrX:54173249
|
T | C | 2 | a0001c0001t0005g0095a0001c0001t0073g0179 | 2 | NA18985.hp1 NA19078.hp1 |
intron_variant | MODIFIER | c.699+9251A>G | FAM120C | ENSG00000184083.12 | transcript | ENST00000375180.7 | protein_coding | 1/15 | chrX | 54173249 | ||||||
chrX:54173423
|
C | CT | 1 | a0001c0001t0017g0005 | 1 | HG01169.hp1 | intron_variant | MODIFIER | c.699+9076dupA | FAM120C | ENSG00000184083.12 | transcript | ENST00000375180.7 | protein_coding | 1/15 | chrX | 54173423 | ||||||
chrX:54173491
|
G | A | 6 | a0001c0001t0018g0115a0001c0001t0018g0116a0001c0001t0018g0151others(3): Show | 6 | HG02572.hp1 HG02615.hp2 HG02809.hp2 others(3): Show |
intron_variant | MODIFIER | c.699+9009C>T | FAM120C | ENSG00000184083.12 | transcript | ENST00000375180.7 | protein_coding | 1/15 | chrX | 54173491 | ||||||
chrX:54173510
|
A | C | 1 | a0001c0001t0004g0021 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.699+8990T>G | FAM120C | ENSG00000184083.12 | transcript | ENST00000375180.7 | protein_coding | 1/15 | chrX | 54173510 | ||||||
chrX:54173538
|
G | A | 1 | a0001c0001t0010g0175 | 1 | NA18980.hp2 | intron_variant | MODIFIER | c.699+8962C>T | FAM120C | ENSG00000184083.12 | transcript | ENST00000375180.7 | protein_coding | 1/15 | chrX | 54173538 | ||||||
chrX:54173571
|
G | GT | 1 | a0001c0001t0017g0005 | 1 | HG01169.hp1 | intron_variant | MODIFIER | c.699+8928dupA | FAM120C | ENSG00000184083.12 | transcript | ENST00000375180.7 | protein_coding | 1/15 | chrX | 54173571 | ||||||
chrX:54173673
|
C | CT | 1 | a0001c0001t0017g0005 | 1 | HG01169.hp1 | intron_variant | MODIFIER | c.699+8826dupA | FAM120C | ENSG00000184083.12 | transcript | ENST00000375180.7 | protein_coding | 1/15 | chrX | 54173673 | ||||||
chrX:54173851
|
C | A | 1 | a0001c0001t0017g0005 | 1 | HG01169.hp1 | intron_variant | MODIFIER | c.699+8649G>T | FAM120C | ENSG00000184083.12 | transcript | ENST00000375180.7 | protein_coding | 1/15 | chrX | 54173851 | ||||||
chrX:54173908
|
A | AG | 1 | a0001c0001t0017g0005 | 1 | HG01169.hp1 | intron_variant | MODIFIER | c.699+8591dupC | FAM120C | ENSG00000184083.12 | transcript | ENST00000375180.7 | protein_coding | 1/15 | chrX | 54173908 | ||||||
chrX:54174429
|
G | A | 1 | a0001c0001t0017g0176 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.699+8071C>T | FAM120C | ENSG00000184083.12 | transcript | ENST00000375180.7 | protein_coding | 1/15 | chrX | 54174429 | ||||||
chrX:54174436
|
T | C | 3 | a0001c0001t0033g0012a0001c0001t0033g0013a0001c0001t0072g0106 | 3 | HG02559.hp2 HG02647.hp1 HG02809.hp1 |
intron_variant | MODIFIER | c.699+8064A>G | FAM120C | ENSG00000184083.12 | transcript | ENST00000375180.7 | protein_coding | 1/15 | chrX | 54174436 | ||||||
chrX:54174477
|
CA | C | 1 | a0001c0001t0017g0005 | 1 | HG01169.hp1 | intron_variant | MODIFIER | c.699+8022delT | FAM120C | ENSG00000184083.12 | transcript | ENST00000375180.7 | protein_coding | 1/15 | chrX | 54174477 | ||||||
chrX:54174537
|
C | CT | 1 | a0001c0001t0017g0005 | 1 | HG01169.hp1 | intron_variant | MODIFIER | c.699+7962dupA | FAM120C | ENSG00000184083.12 | transcript | ENST00000375180.7 | protein_coding | 1/15 | chrX | 54174537 | ||||||
chrX:54174611
|
TA | T | 1 | a0001c0001t0017g0005 | 1 | HG01169.hp1 | intron_variant | MODIFIER | c.699+7888delT | FAM120C | ENSG00000184083.12 | transcript | ENST00000375180.7 | protein_coding | 1/15 | chrX | 54174611 | ||||||
chrX:54174743
|
G | A | 1 | a0001c0001t0068g0096 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.699+7757C>T | FAM120C | ENSG00000184083.12 | transcript | ENST00000375180.7 | protein_coding | 1/15 | chrX | 54174743 | ||||||
chrX:54175027
|
G | A | 1 | a0002c0002t0001g0187 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.699+7473C>T | FAM120C | ENSG00000184083.12 | transcript | ENST00000375180.7 | protein_coding | 1/15 | chrX | 54175027 | ||||||
chrX:54175508
|
T | TA | 1 | a0001c0001t0067g0018 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.699+6991dupT | FAM120C | ENSG00000184083.12 | transcript | ENST00000375180.7 | protein_coding | 1/15 | chrX | 54175508 | ||||||
chrX:54175510
|
C | A | 50 | a0001c0001t0002g0132a0001c0001t0008g0124a0001c0001t0008g0125others(47): Show | 50 | HG00735.hp1 HG00738.hp1 HG01081.hp1 others(47): Show |
intron_variant | MODIFIER | c.699+6990G>T | FAM120C | ENSG00000184083.12 | transcript | ENST00000375180.7 | protein_coding | 1/15 | chrX | 54175510 | ||||||
chrX:54175510
|
C | T | 1 | a0001c0001t0067g0018 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.699+6990G>A | FAM120C | ENSG00000184083.12 | transcript | ENST00000375180.7 | protein_coding | 1/15 | chrX | 54175510 | ||||||
chrX:54175521
|
T | A | 1 | a0001c0001t0012g0104 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.699+6979A>T | FAM120C | ENSG00000184083.12 | transcript | ENST00000375180.7 | protein_coding | 1/15 | chrX | 54175521 | ||||||
chrX:54175548
|
G | A | 1 | a0004c0008t0009g0105 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.699+6952C>T | FAM120C | ENSG00000184083.12 | transcript | ENST00000375180.7 | protein_coding | 1/15 | chrX | 54175548 | ||||||
chrX:54175666
|
GC | G | 1 | a0001c0001t0017g0005 | 1 | HG01169.hp1 | intron_variant | MODIFIER | c.699+6833delG | FAM120C | ENSG00000184083.12 | transcript | ENST00000375180.7 | protein_coding | 1/15 | chrX | 54175666 | ||||||
chrX:54175983
|
G | A | 10 | a0001c0001t0016g0137a0001c0001t0016g0139a0001c0001t0016g0141others(7): Show | 10 | HG01255.hp1 HG01884.hp2 HG02055.hp1 others(7): Show |
intron_variant | MODIFIER | c.699+6517C>T | FAM120C | ENSG00000184083.12 | transcript | ENST00000375180.7 | protein_coding | 1/15 | chrX | 54175983 | ||||||
chrX:54176116
|
T | G | 1 | a0001c0001t0072g0106 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.699+6384A>C | FAM120C | ENSG00000184083.12 | transcript | ENST00000375180.7 | protein_coding | 1/15 | chrX | 54176116 | ||||||
chrX:54176216
|
T | TG | 1 | a0001c0001t0017g0005 | 1 | HG01169.hp1 | intron_variant | MODIFIER | c.699+6283dupC | FAM120C | ENSG00000184083.12 | transcript | ENST00000375180.7 | protein_coding | 1/15 | chrX | 54176216 | ||||||
chrX:54176432
|
C | CA | 13 | a0001c0001t0001g0177a0001c0001t0003g0107a0001c0001t0003g0110others(10): Show | 13 | HG01433.hp1 HG02027.hp1 HG02451.hp1 others(10): Show |
intron_variant | MODIFIER | c.699+6067dupT | FAM120C | ENSG00000184083.12 | transcript | ENST00000375180.7 | protein_coding | 1/15 | chrX | 54176432 | ||||||
chrX:54176432
|
C | CAA | 1 | a0001c0001t0033g0013 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.699+6066_699+6067d others(4): Show |
FAM120C | ENSG00000184083.12 | transcript | ENST00000375180.7 | protein_coding | 1/15 | chrX | 54176432 | ||||||
chrX:54176432
|
CA | C | 3 | a0001c0001t0017g0154a0001c0001t0058g0020a0001c0001t0061g0019 | 3 | HG01069.hp1 HG01257.hp2 HG01952.hp1 |
intron_variant | MODIFIER | c.699+6067delT | FAM120C | ENSG00000184083.12 | transcript | ENST00000375180.7 | protein_coding | 1/15 | chrX | 54176432 | ||||||
chrX:54176568
|
AT | A | 1 | a0001c0001t0017g0005 | 1 | HG01169.hp1 | intron_variant | MODIFIER | c.699+5931delA | FAM120C | ENSG00000184083.12 | transcript | ENST00000375180.7 | protein_coding | 1/15 | chrX | 54176568 | ||||||
chrX:54177042
|
A | G | 1 | a0001c0001t0067g0018 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.699+5458T>C | FAM120C | ENSG00000184083.12 | transcript | ENST00000375180.7 | protein_coding | 1/15 | chrX | 54177042 | ||||||
chrX:54177351
|
GA | G | 1 | a0001c0001t0017g0005 | 1 | HG01169.hp1 | intron_variant | MODIFIER | c.699+5148delT | FAM120C | ENSG00000184083.12 | transcript | ENST00000375180.7 | protein_coding | 1/15 | chrX | 54177351 | ||||||
chrX:54177436
|
CA | C | 1 | a0001c0001t0017g0005 | 1 | HG01169.hp1 | intron_variant | MODIFIER | c.699+5063delT | FAM120C | ENSG00000184083.12 | transcript | ENST00000375180.7 | protein_coding | 1/15 | chrX | 54177436 | ||||||
chrX:54177608
|
GT | G | 1 | a0001c0001t0017g0005 | 1 | HG01169.hp1 | intron_variant | MODIFIER | c.699+4891delA | FAM120C | ENSG00000184083.12 | transcript | ENST00000375180.7 | protein_coding | 1/15 | chrX | 54177608 | ||||||
chrX:54177845
|
G | C | 1 | a0001c0001t0032g0178 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.699+4655C>G | FAM120C | ENSG00000184083.12 | transcript | ENST00000375180.7 | protein_coding | 1/15 | chrX | 54177845 | ||||||
chrX:54177972
|
TG | T | 1 | a0001c0001t0017g0005 | 1 | HG01169.hp1 | intron_variant | MODIFIER | c.699+4527delC | FAM120C | ENSG00000184083.12 | transcript | ENST00000375180.7 | protein_coding | 1/15 | chrX | 54177972 | ||||||
chrX:54178214
|
AG | A | 1 | a0001c0001t0017g0005 | 1 | HG01169.hp1 | intron_variant | MODIFIER | c.699+4285delC | FAM120C | ENSG00000184083.12 | transcript | ENST00000375180.7 | protein_coding | 1/15 | chrX | 54178214 | ||||||
chrX:54178382
|
CA | C | 1 | a0001c0001t0017g0005 | 1 | HG01169.hp1 | intron_variant | MODIFIER | c.699+4117delT | FAM120C | ENSG00000184083.12 | transcript | ENST00000375180.7 | protein_coding | 1/15 | chrX | 54178382 | ||||||
chrX:54178479
|
AT | A | 1 | a0001c0001t0017g0005 | 1 | HG01169.hp1 | intron_variant | MODIFIER | c.699+4020delA | FAM120C | ENSG00000184083.12 | transcript | ENST00000375180.7 | protein_coding | 1/15 | chrX | 54178479 | ||||||
chrX:54178614
|
A | T | 1 | a0001c0001t0017g0005 | 1 | HG01169.hp1 | intron_variant | MODIFIER | c.699+3886T>A | FAM120C | ENSG00000184083.12 | transcript | ENST00000375180.7 | protein_coding | 1/15 | chrX | 54178614 | ||||||
chrX:54178685
|
A | G | 2 | a0001c0001t0033g0012a0001c0001t0033g0013 | 2 | HG02559.hp2 HG02647.hp1 |
intron_variant | MODIFIER | c.699+3815T>C | FAM120C | ENSG00000184083.12 | transcript | ENST00000375180.7 | protein_coding | 1/15 | chrX | 54178685 | ||||||
chrX:54178796
|
G | A | 1 | a0001c0001t0005g0113 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.699+3704C>T | FAM120C | ENSG00000184083.12 | transcript | ENST00000375180.7 | protein_coding | 1/15 | chrX | 54178796 | ||||||
chrX:54178820
|
A | C | 1 | a0001c0001t0048g0126 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.699+3680T>G | FAM120C | ENSG00000184083.12 | transcript | ENST00000375180.7 | protein_coding | 1/15 | chrX | 54178820 | ||||||
chrX:54178857
|
G | A | 2 | a0001c0001t0043g0147a0001c0001t0045g0148 | 2 | HG02922.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.699+3643C>T | FAM120C | ENSG00000184083.12 | transcript | ENST00000375180.7 | protein_coding | 1/15 | chrX | 54178857 | ||||||
chrX:54179048
|
CT | C | 1 | a0001c0001t0017g0005 | 1 | HG01169.hp1 | intron_variant | MODIFIER | c.699+3451delA | FAM120C | ENSG00000184083.12 | transcript | ENST00000375180.7 | protein_coding | 1/15 | chrX | 54179048 | ||||||
chrX:54179167
|
A | G | 1 | a0001c0001t0001g0008 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.699+3333T>C | FAM120C | ENSG00000184083.12 | transcript | ENST00000375180.7 | protein_coding | 1/15 | chrX | 54179167 | ||||||
chrX:54179209
|
T | C | 1 | a0001c0001t0022g0149 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.699+3291A>G | FAM120C | ENSG00000184083.12 | transcript | ENST00000375180.7 | protein_coding | 1/15 | chrX | 54179209 | ||||||
chrX:54179308
|
GA | G | 1 | a0001c0001t0017g0005 | 1 | HG01169.hp1 | intron_variant | MODIFIER | c.699+3191delT | FAM120C | ENSG00000184083.12 | transcript | ENST00000375180.7 | protein_coding | 1/15 | chrX | 54179308 | ||||||
chrX:54179389
|
G | GT | 1 | a0001c0001t0017g0005 | 1 | HG01169.hp1 | intron_variant | MODIFIER | c.699+3110dupA | FAM120C | ENSG00000184083.12 | transcript | ENST00000375180.7 | protein_coding | 1/15 | chrX | 54179389 | ||||||
chrX:54179414
|
A | AG | 1 | a0001c0001t0017g0005 | 1 | HG01169.hp1 | intron_variant | MODIFIER | c.699+3085dupC | FAM120C | ENSG00000184083.12 | transcript | ENST00000375180.7 | protein_coding | 1/15 | chrX | 54179414 | ||||||
chrX:54179443
|
A | AT | 1 | a0001c0001t0017g0005 | 1 | HG01169.hp1 | intron_variant | MODIFIER | c.699+3056dupA | FAM120C | ENSG00000184083.12 | transcript | ENST00000375180.7 | protein_coding | 1/15 | chrX | 54179443 | ||||||
chrX:54179474
|
G | A | 1 | a0001c0001t0035g0114 | 1 | NA18972.hp2 | intron_variant | MODIFIER | c.699+3026C>T | FAM120C | ENSG00000184083.12 | transcript | ENST00000375180.7 | protein_coding | 1/15 | chrX | 54179474 | ||||||
chrX:54179546
|
AG | A | 1 | a0001c0001t0017g0005 | 1 | HG01169.hp1 | intron_variant | MODIFIER | c.699+2953delC | FAM120C | ENSG00000184083.12 | transcript | ENST00000375180.7 | protein_coding | 1/15 | chrX | 54179546 | ||||||
chrX:54179551
|
GTTCT | G | 6 | a0001c0001t0018g0115a0001c0001t0018g0116a0001c0001t0018g0151others(3): Show | 6 | HG02572.hp1 HG02615.hp2 HG02809.hp2 others(3): Show |
intron_variant | MODIFIER | c.699+2945_699+2948d others(6): Show |
FAM120C | ENSG00000184083.12 | transcript | ENST00000375180.7 | protein_coding | 1/15 | chrX | 54179551 | ||||||
chrX:54179644
|
G | T | 1 | a0001c0001t0007g0017 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.699+2856C>A | FAM120C | ENSG00000184083.12 | transcript | ENST00000375180.7 | protein_coding | 1/15 | chrX | 54179644 | ||||||
chrX:54179893
|
G | A | 6 | a0001c0001t0019g0120a0001c0001t0022g0119a0001c0001t0027g0117others(3): Show | 6 | HG03098.hp1 HG03486.hp2 HG03579.hp1 others(3): Show |
intron_variant | MODIFIER | c.699+2607C>T | FAM120C | ENSG00000184083.12 | transcript | ENST00000375180.7 | protein_coding | 1/15 | chrX | 54179893 | ||||||
chrX:54180150
|
C | T | 2 | a0001c0001t0015g0015a0001c0001t0022g0016 | 2 | HG01884.hp1 HG02717.hp1 |
intron_variant | MODIFIER | c.699+2350G>A | FAM120C | ENSG00000184083.12 | transcript | ENST00000375180.7 | protein_coding | 1/15 | chrX | 54180150 | ||||||
chrX:54180159
|
CT | C | 1 | a0001c0001t0017g0005 | 1 | HG01169.hp1 | intron_variant | MODIFIER | c.699+2340delA | FAM120C | ENSG00000184083.12 | transcript | ENST00000375180.7 | protein_coding | 1/15 | chrX | 54180159 | ||||||
chrX:54180343
|
T | TC | 1 | a0001c0001t0017g0005 | 1 | HG01169.hp1 | intron_variant | MODIFIER | c.699+2156dupG | FAM120C | ENSG00000184083.12 | transcript | ENST00000375180.7 | protein_coding | 1/15 | chrX | 54180343 | ||||||
chrX:54180359
|
C | T | 1 | a0001c0001t0002g0153 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.699+2141G>A | FAM120C | ENSG00000184083.12 | transcript | ENST00000375180.7 | protein_coding | 1/15 | chrX | 54180359 | ||||||
chrX:54180366
|
AG | A | 1 | a0001c0001t0017g0005 | 1 | HG01169.hp1 | intron_variant | MODIFIER | c.699+2133delC | FAM120C | ENSG00000184083.12 | transcript | ENST00000375180.7 | protein_coding | 1/15 | chrX | 54180366 | ||||||
chrX:54180667
|
GA | G | 1 | a0001c0001t0017g0005 | 1 | HG01169.hp1 | intron_variant | MODIFIER | c.699+1832delT | FAM120C | ENSG00000184083.12 | transcript | ENST00000375180.7 | protein_coding | 1/15 | chrX | 54180667 | ||||||
chrX:54180676
|
A | G | 1 | a0001c0001t0021g0014 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.699+1824T>C | FAM120C | ENSG00000184083.12 | transcript | ENST00000375180.7 | protein_coding | 1/15 | chrX | 54180676 | ||||||
chrX:54180699
|
C | T | 2 | a0001c0001t0033g0012a0001c0001t0033g0013 | 2 | HG02559.hp2 HG02647.hp1 |
intron_variant | MODIFIER | c.699+1801G>A | FAM120C | ENSG00000184083.12 | transcript | ENST00000375180.7 | protein_coding | 1/15 | chrX | 54180699 | ||||||
chrX:54180716
|
CT | C | 1 | a0001c0001t0017g0005 | 1 | HG01169.hp1 | intron_variant | MODIFIER | c.699+1783delA | FAM120C | ENSG00000184083.12 | transcript | ENST00000375180.7 | protein_coding | 1/15 | chrX | 54180716 | ||||||
chrX:54180818
|
TA | T | 3 | a0001c0001t0008g0124a0001c0001t0008g0125a0001c0001t0011g0123 | 3 | HG02258.hp1 HG02451.hp1 HG02559.hp1 |
intron_variant | MODIFIER | c.699+1681delT | FAM120C | ENSG00000184083.12 | transcript | ENST00000375180.7 | protein_coding | 1/15 | chrX | 54180818 | ||||||
chrX:54181011
|
CA | C | 1 | a0008c0010t0075g0188 | 1 | NA19055.hp1 | intron_variant | MODIFIER | c.699+1488delT | FAM120C | ENSG00000184083.12 | transcript | ENST00000375180.7 | protein_coding | 1/15 | chrX | 54181011 | ||||||
chrX:54181022
|
C | CT | 5 | a0001c0001t0001g0008a0001c0001t0005g0011a0001c0001t0011g0010others(2): Show | 5 | NA18962.hp1 NA18980.hp1 NA19077.hp2 others(2): Show |
intron_variant | MODIFIER | c.699+1477dupA | FAM120C | ENSG00000184083.12 | transcript | ENST00000375180.7 | protein_coding | 1/15 | chrX | 54181022 | ||||||
chrX:54181022
|
CT | C | 60 | a0001c0001t0001g0177a0001c0001t0002g0132a0001c0001t0002g0153others(57): Show | 61 | HG00558.hp2 HG00609.hp1 HG00621.hp1 others(58): Show |
intron_variant | MODIFIER | c.699+1477delA | FAM120C | ENSG00000184083.12 | transcript | ENST00000375180.7 | protein_coding | 1/15 | chrX | 54181022 | ||||||
chrX:54181039
|
AC | A | 1 | a0001c0001t0017g0005 | 1 | HG01169.hp1 | intron_variant | MODIFIER | c.699+1460delG | FAM120C | ENSG00000184083.12 | transcript | ENST00000375180.7 | protein_coding | 1/15 | chrX | 54181039 | ||||||
chrX:54181306
|
C | T | 1 | a0005c0007t0034g0007 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.699+1194G>A | FAM120C | ENSG00000184083.12 | transcript | ENST00000375180.7 | protein_coding | 1/15 | chrX | 54181306 | ||||||
chrX:54181397
|
A | G | 1 | a0001c0001t0004g0006 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.699+1103T>C | FAM120C | ENSG00000184083.12 | transcript | ENST00000375180.7 | protein_coding | 1/15 | chrX | 54181397 | ||||||
chrX:54181674
|
G | GT | 1 | a0008c0010t0075g0188 | 1 | NA19055.hp1 | intron_variant | MODIFIER | c.699+825dupA | FAM120C | ENSG00000184083.12 | transcript | ENST00000375180.7 | protein_coding | 1/15 | chrX | 54181674 | ||||||
chrX:54181679
|
G | A | 29 | a0001c0001t0001g0177a0001c0001t0002g0153a0001c0001t0002g0159others(26): Show | 30 | HG00558.hp2 HG00609.hp1 HG00621.hp1 others(27): Show |
intron_variant | MODIFIER | c.699+821C>T | FAM120C | ENSG00000184083.12 | transcript | ENST00000375180.7 | protein_coding | 1/15 | chrX | 54181679 | ||||||
chrX:54181701
|
TC | T | 1 | a0001c0001t0017g0005 | 1 | HG01169.hp1 | intron_variant | MODIFIER | c.699+798delG | FAM120C | ENSG00000184083.12 | transcript | ENST00000375180.7 | protein_coding | 1/15 | chrX | 54181701 | ||||||
chrX:54181754
|
A | AG | 1 | a0001c0001t0017g0005 | 1 | HG01169.hp1 | intron_variant | MODIFIER | c.699+745dupC | FAM120C | ENSG00000184083.12 | transcript | ENST00000375180.7 | protein_coding | 1/15 | chrX | 54181754 | ||||||
chrX:54181872
|
T | A | 1 | a0008c0010t0075g0188 | 1 | NA19055.hp1 | intron_variant | MODIFIER | c.699+628A>T | FAM120C | ENSG00000184083.12 | transcript | ENST00000375180.7 | protein_coding | 1/15 | chrX | 54181872 | ||||||
chrX:54181876
|
A | AC | 1 | a0001c0001t0017g0005 | 1 | HG01169.hp1 | intron_variant | MODIFIER | c.699+623dupG | FAM120C | ENSG00000184083.12 | transcript | ENST00000375180.7 | protein_coding | 1/15 | chrX | 54181876 | ||||||
chrX:54181934
|
T | C | 1 | a0001c0001t0073g0179 | 1 | NA19078.hp1 | intron_variant | MODIFIER | c.699+566A>G | FAM120C | ENSG00000184083.12 | transcript | ENST00000375180.7 | protein_coding | 1/15 | chrX | 54181934 | ||||||
chrX:54182059
|
T | TTCA | 1 | a0001c0001t0004g0180 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.699+438_699+440dup others(3): Show |
FAM120C | ENSG00000184083.12 | transcript | ENST00000375180.7 | protein_coding | 1/15 | chrX | 54182059 | ||||||
chrX:54182085
|
C | A | 1 | a0001c0001t0003g0181 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.699+415G>T | FAM120C | ENSG00000184083.12 | transcript | ENST00000375180.7 | protein_coding | 1/15 | chrX | 54182085 | ||||||
chrX:54182250
|
AG | A | 1 | a0008c0010t0075g0188 | 1 | NA19055.hp1 | intron_variant | MODIFIER | c.699+249delC | FAM120C | ENSG00000184083.12 | transcript | ENST00000375180.7 | protein_coding | 1/15 | chrX | 54182250 | ||||||
chrX:54182261
|
G | A | 1 | a0001c0001t0062g0182 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.699+239C>T | FAM120C | ENSG00000184083.12 | transcript | ENST00000375180.7 | protein_coding | 1/15 | chrX | 54182261 | ||||||
chrX:54182447
|
T | C | 1 | a0001c0001t0042g0183 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.699+53A>G | FAM120C | ENSG00000184083.12 | transcript | ENST00000375180.7 | protein_coding | 1/15 | chrX | 54182447 | ||||||
chrX:54182487
|
G | GC | 1 | a0008c0010t0075g0188 | 1 | NA19055.hp1 | intron_variant | MODIFIER | c.699+12dupG | FAM120C | ENSG00000184083.12 | transcript | ENST00000375180.7 | protein_coding | 1/15 | chrX | 54182487 |