Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| geneid | 7102 |
|---|---|
| ensemblid | ENSG00000156298.13 |
| hgncid | 11854 |
| symbol | TSPAN7 |
| name | tetraspanin 7 |
| refseq_nuc | NM_004615.4 |
| refseq_prot | NP_004606.2 |
| ensembl_nuc | ENST00000378482.7 |
| ensembl_prot | ENSP00000367743.2 |
| mane_status | MANE Select |
| chr | chrX |
| start | 38561542 |
| end | 38688918 |
| strand | + |
| ver | v1.2 |
| region | chrX:38561542-38688918 |
| region5000 | chrX:38556542-38693918 |
| regionname0 | TSPAN7_chrX_38561542_38688918 |
| regionname5000 | TSPAN7_chrX_38556542_38693918 |
| ahapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 249 | 222 | 64 | 36 | 87 | 9 | 24 | 70 | TSPAN7_chrX_38556542_38693918 | TSPAN7 | copy fasta | chrX | 38556542 | 38693918 |
| a0002 | 0/0 | 211 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | TSPAN7_chrX_38556542_38693918 | TSPAN7 | copy fasta | chrX | 38556542 | 38693918 |
| chapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| c0001 | 1/1 | 750 | 207 | 49 | 36 | 87 | 9 | 24 | TSPAN7_chrX_38556542_38693918 | TSPAN7 | copy fasta | chrX | 38556542 | 38693918 |
| c0002 | 0/0 | 750 | 9 | 9 | 0 | 0 | 0 | 0 | TSPAN7_chrX_38556542_38693918 | TSPAN7 | copy fasta | chrX | 38556542 | 38693918 |
| c0003 | 0/0 | 750 | 6 | 6 | 0 | 0 | 0 | 0 | TSPAN7_chrX_38556542_38693918 | TSPAN7 | copy fasta | chrX | 38556542 | 38693918 |
| c0004 | 0/0 | 751 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN7_chrX_38556542_38693918 | TSPAN7 | copy fasta | chrX | 38556542 | 38693918 |
| thapid | grch38chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| t0001 | 0/1 | 993 | 171 | 45 | 29 | 72 | 6 | 18 | TSPAN7_chrX_38556542_38693918 | TSPAN7 | copy fasta | chrX | 38556542 | 38693918 |
| t0002 | 1/0 | 993 | 47 | 14 | 7 | 16 | 3 | 6 | TSPAN7_chrX_38556542_38693918 | TSPAN7 | copy fasta | chrX | 38556542 | 38693918 |
| t0003 | 0/0 | 993 | 3 | 3 | 0 | 0 | 0 | 0 | TSPAN7_chrX_38556542_38693918 | TSPAN7 | copy fasta | chrX | 38556542 | 38693918 |
| t0004 | 0/0 | 993 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN7_chrX_38556542_38693918 | TSPAN7 | copy fasta | chrX | 38556542 | 38693918 |
| t0005 | 0/0 | 993 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN7_chrX_38556542_38693918 | TSPAN7 | copy fasta | chrX | 38556542 | 38693918 |
| ghapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| g0001 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TSPAN7_chrX_38556542_38693918 | TSPAN7 | chrX | 38556542 | 38693918 |
| g0002 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TSPAN7_chrX_38556542_38693918 | TSPAN7 | chrX | 38556542 | 38693918 |
| g0003 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | TSPAN7_chrX_38556542_38693918 | TSPAN7 | chrX | 38556542 | 38693918 |
| g0004 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | TSPAN7_chrX_38556542_38693918 | TSPAN7 | chrX | 38556542 | 38693918 |
| g0005 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | TSPAN7_chrX_38556542_38693918 | TSPAN7 | chrX | 38556542 | 38693918 |
| g0006 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | TSPAN7_chrX_38556542_38693918 | TSPAN7 | chrX | 38556542 | 38693918 |
| g0007 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TSPAN7_chrX_38556542_38693918 | TSPAN7 | chrX | 38556542 | 38693918 |
| g0008 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN7_chrX_38556542_38693918 | TSPAN7 | chrX | 38556542 | 38693918 |
| g0009 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN7_chrX_38556542_38693918 | TSPAN7 | chrX | 38556542 | 38693918 |
| g0010 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN7_chrX_38556542_38693918 | TSPAN7 | chrX | 38556542 | 38693918 |
| g0011 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN7_chrX_38556542_38693918 | TSPAN7 | chrX | 38556542 | 38693918 |
| g0012 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN7_chrX_38556542_38693918 | TSPAN7 | chrX | 38556542 | 38693918 |
| g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN7_chrX_38556542_38693918 | TSPAN7 | chrX | 38556542 | 38693918 |
| g0014 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN7_chrX_38556542_38693918 | TSPAN7 | chrX | 38556542 | 38693918 |
| g0015 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TSPAN7_chrX_38556542_38693918 | TSPAN7 | chrX | 38556542 | 38693918 |
| g0016 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN7_chrX_38556542_38693918 | TSPAN7 | chrX | 38556542 | 38693918 |
| g0017 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN7_chrX_38556542_38693918 | TSPAN7 | chrX | 38556542 | 38693918 |
| g0018 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN7_chrX_38556542_38693918 | TSPAN7 | chrX | 38556542 | 38693918 |
| g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN7_chrX_38556542_38693918 | TSPAN7 | chrX | 38556542 | 38693918 |
| g0020 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN7_chrX_38556542_38693918 | TSPAN7 | chrX | 38556542 | 38693918 |
| g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN7_chrX_38556542_38693918 | TSPAN7 | chrX | 38556542 | 38693918 |
| g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN7_chrX_38556542_38693918 | TSPAN7 | chrX | 38556542 | 38693918 |
| g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN7_chrX_38556542_38693918 | TSPAN7 | chrX | 38556542 | 38693918 |
| g0024 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TSPAN7_chrX_38556542_38693918 | TSPAN7 | chrX | 38556542 | 38693918 |
| g0025 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TSPAN7_chrX_38556542_38693918 | TSPAN7 | chrX | 38556542 | 38693918 |
| g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN7_chrX_38556542_38693918 | TSPAN7 | chrX | 38556542 | 38693918 |
| g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN7_chrX_38556542_38693918 | TSPAN7 | chrX | 38556542 | 38693918 |
| g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN7_chrX_38556542_38693918 | TSPAN7 | chrX | 38556542 | 38693918 |
| g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN7_chrX_38556542_38693918 | TSPAN7 | chrX | 38556542 | 38693918 |
| g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN7_chrX_38556542_38693918 | TSPAN7 | chrX | 38556542 | 38693918 |
| g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN7_chrX_38556542_38693918 | TSPAN7 | chrX | 38556542 | 38693918 |
| g0032 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TSPAN7_chrX_38556542_38693918 | TSPAN7 | chrX | 38556542 | 38693918 |
| g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN7_chrX_38556542_38693918 | TSPAN7 | chrX | 38556542 | 38693918 |
| g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN7_chrX_38556542_38693918 | TSPAN7 | chrX | 38556542 | 38693918 |
| g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN7_chrX_38556542_38693918 | TSPAN7 | chrX | 38556542 | 38693918 |
| g0036 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN7_chrX_38556542_38693918 | TSPAN7 | chrX | 38556542 | 38693918 |
| g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN7_chrX_38556542_38693918 | TSPAN7 | chrX | 38556542 | 38693918 |
| g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN7_chrX_38556542_38693918 | TSPAN7 | chrX | 38556542 | 38693918 |
| g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN7_chrX_38556542_38693918 | TSPAN7 | chrX | 38556542 | 38693918 |
| g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN7_chrX_38556542_38693918 | TSPAN7 | chrX | 38556542 | 38693918 |
| g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN7_chrX_38556542_38693918 | TSPAN7 | chrX | 38556542 | 38693918 |
| g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN7_chrX_38556542_38693918 | TSPAN7 | chrX | 38556542 | 38693918 |
| g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN7_chrX_38556542_38693918 | TSPAN7 | chrX | 38556542 | 38693918 |
| g0044 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN7_chrX_38556542_38693918 | TSPAN7 | chrX | 38556542 | 38693918 |
| g0045 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TSPAN7_chrX_38556542_38693918 | TSPAN7 | chrX | 38556542 | 38693918 |
| g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN7_chrX_38556542_38693918 | TSPAN7 | chrX | 38556542 | 38693918 |
| g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN7_chrX_38556542_38693918 | TSPAN7 | chrX | 38556542 | 38693918 |
| g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN7_chrX_38556542_38693918 | TSPAN7 | chrX | 38556542 | 38693918 |
| g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN7_chrX_38556542_38693918 | TSPAN7 | chrX | 38556542 | 38693918 |
| g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN7_chrX_38556542_38693918 | TSPAN7 | chrX | 38556542 | 38693918 |
| g0051 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TSPAN7_chrX_38556542_38693918 | TSPAN7 | chrX | 38556542 | 38693918 |
| g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN7_chrX_38556542_38693918 | TSPAN7 | chrX | 38556542 | 38693918 |
| g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN7_chrX_38556542_38693918 | TSPAN7 | chrX | 38556542 | 38693918 |
| g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN7_chrX_38556542_38693918 | TSPAN7 | chrX | 38556542 | 38693918 |
| g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN7_chrX_38556542_38693918 | TSPAN7 | chrX | 38556542 | 38693918 |
| g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN7_chrX_38556542_38693918 | TSPAN7 | chrX | 38556542 | 38693918 |
| g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN7_chrX_38556542_38693918 | TSPAN7 | chrX | 38556542 | 38693918 |
| g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN7_chrX_38556542_38693918 | TSPAN7 | chrX | 38556542 | 38693918 |
| g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN7_chrX_38556542_38693918 | TSPAN7 | chrX | 38556542 | 38693918 |
| g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN7_chrX_38556542_38693918 | TSPAN7 | chrX | 38556542 | 38693918 |
| g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN7_chrX_38556542_38693918 | TSPAN7 | chrX | 38556542 | 38693918 |
| g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN7_chrX_38556542_38693918 | TSPAN7 | chrX | 38556542 | 38693918 |
| g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN7_chrX_38556542_38693918 | TSPAN7 | chrX | 38556542 | 38693918 |
| g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN7_chrX_38556542_38693918 | TSPAN7 | chrX | 38556542 | 38693918 |
| g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN7_chrX_38556542_38693918 | TSPAN7 | chrX | 38556542 | 38693918 |
| g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN7_chrX_38556542_38693918 | TSPAN7 | chrX | 38556542 | 38693918 |
| g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN7_chrX_38556542_38693918 | TSPAN7 | chrX | 38556542 | 38693918 |
| g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN7_chrX_38556542_38693918 | TSPAN7 | chrX | 38556542 | 38693918 |
| g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN7_chrX_38556542_38693918 | TSPAN7 | chrX | 38556542 | 38693918 |
| g0070 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TSPAN7_chrX_38556542_38693918 | TSPAN7 | chrX | 38556542 | 38693918 |
| g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN7_chrX_38556542_38693918 | TSPAN7 | chrX | 38556542 | 38693918 |
| g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN7_chrX_38556542_38693918 | TSPAN7 | chrX | 38556542 | 38693918 |
| g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN7_chrX_38556542_38693918 | TSPAN7 | chrX | 38556542 | 38693918 |
| g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN7_chrX_38556542_38693918 | TSPAN7 | chrX | 38556542 | 38693918 |
| g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN7_chrX_38556542_38693918 | TSPAN7 | chrX | 38556542 | 38693918 |
| g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN7_chrX_38556542_38693918 | TSPAN7 | chrX | 38556542 | 38693918 |
| g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN7_chrX_38556542_38693918 | TSPAN7 | chrX | 38556542 | 38693918 |
| g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN7_chrX_38556542_38693918 | TSPAN7 | chrX | 38556542 | 38693918 |
| g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN7_chrX_38556542_38693918 | TSPAN7 | chrX | 38556542 | 38693918 |
| g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN7_chrX_38556542_38693918 | TSPAN7 | chrX | 38556542 | 38693918 |
| g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN7_chrX_38556542_38693918 | TSPAN7 | chrX | 38556542 | 38693918 |
| g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN7_chrX_38556542_38693918 | TSPAN7 | chrX | 38556542 | 38693918 |
| g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN7_chrX_38556542_38693918 | TSPAN7 | chrX | 38556542 | 38693918 |
| g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN7_chrX_38556542_38693918 | TSPAN7 | chrX | 38556542 | 38693918 |
| g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN7_chrX_38556542_38693918 | TSPAN7 | chrX | 38556542 | 38693918 |
| g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN7_chrX_38556542_38693918 | TSPAN7 | chrX | 38556542 | 38693918 |
| g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN7_chrX_38556542_38693918 | TSPAN7 | chrX | 38556542 | 38693918 |
| g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN7_chrX_38556542_38693918 | TSPAN7 | chrX | 38556542 | 38693918 |
| g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN7_chrX_38556542_38693918 | TSPAN7 | chrX | 38556542 | 38693918 |
| g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN7_chrX_38556542_38693918 | TSPAN7 | chrX | 38556542 | 38693918 |
| g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN7_chrX_38556542_38693918 | TSPAN7 | chrX | 38556542 | 38693918 |
| g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN7_chrX_38556542_38693918 | TSPAN7 | chrX | 38556542 | 38693918 |
| g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN7_chrX_38556542_38693918 | TSPAN7 | chrX | 38556542 | 38693918 |
| g0094 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TSPAN7_chrX_38556542_38693918 | TSPAN7 | chrX | 38556542 | 38693918 |
| g0095 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TSPAN7_chrX_38556542_38693918 | TSPAN7 | chrX | 38556542 | 38693918 |
| g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN7_chrX_38556542_38693918 | TSPAN7 | chrX | 38556542 | 38693918 |
| g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN7_chrX_38556542_38693918 | TSPAN7 | chrX | 38556542 | 38693918 |
| g0098 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TSPAN7_chrX_38556542_38693918 | TSPAN7 | chrX | 38556542 | 38693918 |
| g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN7_chrX_38556542_38693918 | TSPAN7 | chrX | 38556542 | 38693918 |
| g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN7_chrX_38556542_38693918 | TSPAN7 | chrX | 38556542 | 38693918 |
| g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN7_chrX_38556542_38693918 | TSPAN7 | chrX | 38556542 | 38693918 |
| g0102 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TSPAN7_chrX_38556542_38693918 | TSPAN7 | chrX | 38556542 | 38693918 |
| g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN7_chrX_38556542_38693918 | TSPAN7 | chrX | 38556542 | 38693918 |
| g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN7_chrX_38556542_38693918 | TSPAN7 | chrX | 38556542 | 38693918 |
| g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN7_chrX_38556542_38693918 | TSPAN7 | chrX | 38556542 | 38693918 |
| g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN7_chrX_38556542_38693918 | TSPAN7 | chrX | 38556542 | 38693918 |
| g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN7_chrX_38556542_38693918 | TSPAN7 | chrX | 38556542 | 38693918 |
| g0108 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN7_chrX_38556542_38693918 | TSPAN7 | chrX | 38556542 | 38693918 |
| g0109 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TSPAN7_chrX_38556542_38693918 | TSPAN7 | chrX | 38556542 | 38693918 |
| g0110 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TSPAN7_chrX_38556542_38693918 | TSPAN7 | chrX | 38556542 | 38693918 |
| g0111 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TSPAN7_chrX_38556542_38693918 | TSPAN7 | chrX | 38556542 | 38693918 |
| g0112 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TSPAN7_chrX_38556542_38693918 | TSPAN7 | chrX | 38556542 | 38693918 |
| g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN7_chrX_38556542_38693918 | TSPAN7 | chrX | 38556542 | 38693918 |
| g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN7_chrX_38556542_38693918 | TSPAN7 | chrX | 38556542 | 38693918 |
| g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN7_chrX_38556542_38693918 | TSPAN7 | chrX | 38556542 | 38693918 |
| g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN7_chrX_38556542_38693918 | TSPAN7 | chrX | 38556542 | 38693918 |
| g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN7_chrX_38556542_38693918 | TSPAN7 | chrX | 38556542 | 38693918 |
| g0118 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN7_chrX_38556542_38693918 | TSPAN7 | chrX | 38556542 | 38693918 |
| g0119 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN7_chrX_38556542_38693918 | TSPAN7 | chrX | 38556542 | 38693918 |
| g0120 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN7_chrX_38556542_38693918 | TSPAN7 | chrX | 38556542 | 38693918 |
| g0121 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN7_chrX_38556542_38693918 | TSPAN7 | chrX | 38556542 | 38693918 |
| g0122 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN7_chrX_38556542_38693918 | TSPAN7 | chrX | 38556542 | 38693918 |
| g0123 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN7_chrX_38556542_38693918 | TSPAN7 | chrX | 38556542 | 38693918 |
| g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN7_chrX_38556542_38693918 | TSPAN7 | chrX | 38556542 | 38693918 |
| g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN7_chrX_38556542_38693918 | TSPAN7 | chrX | 38556542 | 38693918 |
| g0126 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | TSPAN7_chrX_38556542_38693918 | TSPAN7 | chrX | 38556542 | 38693918 |
| g0127 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TSPAN7_chrX_38556542_38693918 | TSPAN7 | chrX | 38556542 | 38693918 |
| g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN7_chrX_38556542_38693918 | TSPAN7 | chrX | 38556542 | 38693918 |
| g0129 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN7_chrX_38556542_38693918 | TSPAN7 | chrX | 38556542 | 38693918 |
| g0130 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TSPAN7_chrX_38556542_38693918 | TSPAN7 | chrX | 38556542 | 38693918 |
| g0131 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TSPAN7_chrX_38556542_38693918 | TSPAN7 | chrX | 38556542 | 38693918 |
| g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN7_chrX_38556542_38693918 | TSPAN7 | chrX | 38556542 | 38693918 |
| g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN7_chrX_38556542_38693918 | TSPAN7 | chrX | 38556542 | 38693918 |
| g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN7_chrX_38556542_38693918 | TSPAN7 | chrX | 38556542 | 38693918 |
| g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN7_chrX_38556542_38693918 | TSPAN7 | chrX | 38556542 | 38693918 |
| g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN7_chrX_38556542_38693918 | TSPAN7 | chrX | 38556542 | 38693918 |
| g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN7_chrX_38556542_38693918 | TSPAN7 | chrX | 38556542 | 38693918 |
| g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN7_chrX_38556542_38693918 | TSPAN7 | chrX | 38556542 | 38693918 |
| g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN7_chrX_38556542_38693918 | TSPAN7 | chrX | 38556542 | 38693918 |
| g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN7_chrX_38556542_38693918 | TSPAN7 | chrX | 38556542 | 38693918 |
| g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN7_chrX_38556542_38693918 | TSPAN7 | chrX | 38556542 | 38693918 |
| g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN7_chrX_38556542_38693918 | TSPAN7 | chrX | 38556542 | 38693918 |
| g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN7_chrX_38556542_38693918 | TSPAN7 | chrX | 38556542 | 38693918 |
| g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN7_chrX_38556542_38693918 | TSPAN7 | chrX | 38556542 | 38693918 |
| g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN7_chrX_38556542_38693918 | TSPAN7 | chrX | 38556542 | 38693918 |
| g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN7_chrX_38556542_38693918 | TSPAN7 | chrX | 38556542 | 38693918 |
| g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN7_chrX_38556542_38693918 | TSPAN7 | chrX | 38556542 | 38693918 |
| g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN7_chrX_38556542_38693918 | TSPAN7 | chrX | 38556542 | 38693918 |
| g0149 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TSPAN7_chrX_38556542_38693918 | TSPAN7 | chrX | 38556542 | 38693918 |
| g0150 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN7_chrX_38556542_38693918 | TSPAN7 | chrX | 38556542 | 38693918 |
| g0151 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN7_chrX_38556542_38693918 | TSPAN7 | chrX | 38556542 | 38693918 |
| g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN7_chrX_38556542_38693918 | TSPAN7 | chrX | 38556542 | 38693918 |
| g0153 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TSPAN7_chrX_38556542_38693918 | TSPAN7 | chrX | 38556542 | 38693918 |
| g0154 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TSPAN7_chrX_38556542_38693918 | TSPAN7 | chrX | 38556542 | 38693918 |
| g0155 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN7_chrX_38556542_38693918 | TSPAN7 | chrX | 38556542 | 38693918 |
| g0156 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TSPAN7_chrX_38556542_38693918 | TSPAN7 | chrX | 38556542 | 38693918 |
| g0157 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TSPAN7_chrX_38556542_38693918 | TSPAN7 | chrX | 38556542 | 38693918 |
| g0158 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | TSPAN7_chrX_38556542_38693918 | TSPAN7 | chrX | 38556542 | 38693918 |
| g0159 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TSPAN7_chrX_38556542_38693918 | TSPAN7 | chrX | 38556542 | 38693918 |
| g0160 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TSPAN7_chrX_38556542_38693918 | TSPAN7 | chrX | 38556542 | 38693918 |
| g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN7_chrX_38556542_38693918 | TSPAN7 | chrX | 38556542 | 38693918 |
| g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN7_chrX_38556542_38693918 | TSPAN7 | chrX | 38556542 | 38693918 |
| g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN7_chrX_38556542_38693918 | TSPAN7 | chrX | 38556542 | 38693918 |
| g0164 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN7_chrX_38556542_38693918 | TSPAN7 | chrX | 38556542 | 38693918 |
| g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN7_chrX_38556542_38693918 | TSPAN7 | chrX | 38556542 | 38693918 |
| g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN7_chrX_38556542_38693918 | TSPAN7 | chrX | 38556542 | 38693918 |
| g0167 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN7_chrX_38556542_38693918 | TSPAN7 | chrX | 38556542 | 38693918 |
| g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN7_chrX_38556542_38693918 | TSPAN7 | chrX | 38556542 | 38693918 |
| g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN7_chrX_38556542_38693918 | TSPAN7 | chrX | 38556542 | 38693918 |
| g0170 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN7_chrX_38556542_38693918 | TSPAN7 | chrX | 38556542 | 38693918 |
| g0171 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN7_chrX_38556542_38693918 | TSPAN7 | chrX | 38556542 | 38693918 |
| g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN7_chrX_38556542_38693918 | TSPAN7 | chrX | 38556542 | 38693918 |
| g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN7_chrX_38556542_38693918 | TSPAN7 | chrX | 38556542 | 38693918 |
| g0174 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TSPAN7_chrX_38556542_38693918 | TSPAN7 | chrX | 38556542 | 38693918 |
| g0175 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN7_chrX_38556542_38693918 | TSPAN7 | chrX | 38556542 | 38693918 |
| g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN7_chrX_38556542_38693918 | TSPAN7 | chrX | 38556542 | 38693918 |
| g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN7_chrX_38556542_38693918 | TSPAN7 | chrX | 38556542 | 38693918 |
| g0178 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN7_chrX_38556542_38693918 | TSPAN7 | chrX | 38556542 | 38693918 |
| g0179 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN7_chrX_38556542_38693918 | TSPAN7 | chrX | 38556542 | 38693918 |
| g0180 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN7_chrX_38556542_38693918 | TSPAN7 | chrX | 38556542 | 38693918 |
| g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN7_chrX_38556542_38693918 | TSPAN7 | chrX | 38556542 | 38693918 |
| g0182 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TSPAN7_chrX_38556542_38693918 | TSPAN7 | chrX | 38556542 | 38693918 |
| g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN7_chrX_38556542_38693918 | TSPAN7 | chrX | 38556542 | 38693918 |
| g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN7_chrX_38556542_38693918 | TSPAN7 | chrX | 38556542 | 38693918 |
| g0185 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TSPAN7_chrX_38556542_38693918 | TSPAN7 | chrX | 38556542 | 38693918 |
| g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN7_chrX_38556542_38693918 | TSPAN7 | chrX | 38556542 | 38693918 |
| g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN7_chrX_38556542_38693918 | TSPAN7 | chrX | 38556542 | 38693918 |
| g0188 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TSPAN7_chrX_38556542_38693918 | TSPAN7 | chrX | 38556542 | 38693918 |
| g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN7_chrX_38556542_38693918 | TSPAN7 | chrX | 38556542 | 38693918 |
| g0190 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TSPAN7_chrX_38556542_38693918 | TSPAN7 | chrX | 38556542 | 38693918 |
| g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN7_chrX_38556542_38693918 | TSPAN7 | chrX | 38556542 | 38693918 |
| g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN7_chrX_38556542_38693918 | TSPAN7 | chrX | 38556542 | 38693918 |
| g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN7_chrX_38556542_38693918 | TSPAN7 | chrX | 38556542 | 38693918 |
| g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN7_chrX_38556542_38693918 | TSPAN7 | chrX | 38556542 | 38693918 |
| g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN7_chrX_38556542_38693918 | TSPAN7 | chrX | 38556542 | 38693918 |
| g0196 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TSPAN7_chrX_38556542_38693918 | TSPAN7 | chrX | 38556542 | 38693918 |
| g0197 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN7_chrX_38556542_38693918 | TSPAN7 | chrX | 38556542 | 38693918 |
| g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN7_chrX_38556542_38693918 | TSPAN7 | chrX | 38556542 | 38693918 |
| g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN7_chrX_38556542_38693918 | TSPAN7 | chrX | 38556542 | 38693918 |
| g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN7_chrX_38556542_38693918 | TSPAN7 | chrX | 38556542 | 38693918 |
| g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN7_chrX_38556542_38693918 | TSPAN7 | chrX | 38556542 | 38693918 |
| g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN7_chrX_38556542_38693918 | TSPAN7 | chrX | 38556542 | 38693918 |
| g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN7_chrX_38556542_38693918 | TSPAN7 | chrX | 38556542 | 38693918 |
| g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN7_chrX_38556542_38693918 | TSPAN7 | chrX | 38556542 | 38693918 |
| g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN7_chrX_38556542_38693918 | TSPAN7 | chrX | 38556542 | 38693918 |
| g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN7_chrX_38556542_38693918 | TSPAN7 | chrX | 38556542 | 38693918 |
| g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN7_chrX_38556542_38693918 | TSPAN7 | chrX | 38556542 | 38693918 |
| g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN7_chrX_38556542_38693918 | TSPAN7 | chrX | 38556542 | 38693918 |
| g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN7_chrX_38556542_38693918 | TSPAN7 | chrX | 38556542 | 38693918 |
| g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN7_chrX_38556542_38693918 | TSPAN7 | chrX | 38556542 | 38693918 |
| g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN7_chrX_38556542_38693918 | TSPAN7 | chrX | 38556542 | 38693918 |
| g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN7_chrX_38556542_38693918 | TSPAN7 | chrX | 38556542 | 38693918 |
| g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN7_chrX_38556542_38693918 | TSPAN7 | chrX | 38556542 | 38693918 |
| g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN7_chrX_38556542_38693918 | TSPAN7 | chrX | 38556542 | 38693918 |
| g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN7_chrX_38556542_38693918 | TSPAN7 | chrX | 38556542 | 38693918 |
| g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN7_chrX_38556542_38693918 | TSPAN7 | chrX | 38556542 | 38693918 |
| achapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 750 | 207 | 49 | 36 | 87 | 9 | 24 | TSPAN7_chrX_38556542_38693918 | TSPAN7 | copy fasta | chrX | 38556542 | 38693918 |
| a0001c0002 | 0/0 | 750 | 9 | 9 | 0 | 0 | 0 | 0 | TSPAN7_chrX_38556542_38693918 | TSPAN7 | copy fasta | chrX | 38556542 | 38693918 |
| a0001c0003 | 0/0 | 750 | 6 | 6 | 0 | 0 | 0 | 0 | TSPAN7_chrX_38556542_38693918 | TSPAN7 | copy fasta | chrX | 38556542 | 38693918 |
| a0002c0004 | 0/0 | 751 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN7_chrX_38556542_38693918 | TSPAN7 | copy fasta | chrX | 38556542 | 38693918 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/1 | 1742 | 156 | 31 | 29 | 71 | 6 | 18 | TSPAN7_chrX_38556542_38693918 | TSPAN7 | copy fasta | chrX | 38556542 | 38693918 |
| a0001c0001t0002 | 1/0 | 1742 | 47 | 14 | 7 | 16 | 3 | 6 | TSPAN7_chrX_38556542_38693918 | TSPAN7 | copy fasta | chrX | 38556542 | 38693918 |
| a0001c0001t0003 | 0/0 | 1742 | 3 | 3 | 0 | 0 | 0 | 0 | TSPAN7_chrX_38556542_38693918 | TSPAN7 | copy fasta | chrX | 38556542 | 38693918 |
| a0001c0001t0005 | 0/0 | 1742 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN7_chrX_38556542_38693918 | TSPAN7 | copy fasta | chrX | 38556542 | 38693918 |
| a0001c0002t0001 | 0/0 | 1742 | 9 | 9 | 0 | 0 | 0 | 0 | TSPAN7_chrX_38556542_38693918 | TSPAN7 | copy fasta | chrX | 38556542 | 38693918 |
| a0001c0003t0001 | 0/0 | 1742 | 5 | 5 | 0 | 0 | 0 | 0 | TSPAN7_chrX_38556542_38693918 | TSPAN7 | copy fasta | chrX | 38556542 | 38693918 |
| a0001c0003t0004 | 0/0 | 1742 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN7_chrX_38556542_38693918 | TSPAN7 | copy fasta | chrX | 38556542 | 38693918 |
| a0002c0004t0001 | 0/0 | 1743 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN7_chrX_38556542_38693918 | TSPAN7 | copy fasta | chrX | 38556542 | 38693918 |
| actghapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0002 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TSPAN7_chrX_38556542_38693918 | TSPAN7 | chrX | 38556542 | 38693918 |
| a0001c0001t0001g0003 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | TSPAN7_chrX_38556542_38693918 | TSPAN7 | chrX | 38556542 | 38693918 |
| a0001c0001t0001g0004 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | TSPAN7_chrX_38556542_38693918 | TSPAN7 | chrX | 38556542 | 38693918 |
| a0001c0001t0001g0005 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | TSPAN7_chrX_38556542_38693918 | TSPAN7 | chrX | 38556542 | 38693918 |
| a0001c0001t0001g0006 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | TSPAN7_chrX_38556542_38693918 | TSPAN7 | chrX | 38556542 | 38693918 |
| a0001c0001t0001g0007 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TSPAN7_chrX_38556542_38693918 | TSPAN7 | chrX | 38556542 | 38693918 |
| a0001c0001t0001g0008 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN7_chrX_38556542_38693918 | TSPAN7 | chrX | 38556542 | 38693918 |
| a0001c0001t0001g0009 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN7_chrX_38556542_38693918 | TSPAN7 | chrX | 38556542 | 38693918 |
| a0001c0001t0001g0010 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN7_chrX_38556542_38693918 | TSPAN7 | chrX | 38556542 | 38693918 |
| a0001c0001t0001g0011 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN7_chrX_38556542_38693918 | TSPAN7 | chrX | 38556542 | 38693918 |
| a0001c0001t0001g0012 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN7_chrX_38556542_38693918 | TSPAN7 | chrX | 38556542 | 38693918 |
| a0001c0001t0001g0014 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN7_chrX_38556542_38693918 | TSPAN7 | chrX | 38556542 | 38693918 |
| a0001c0001t0001g0015 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TSPAN7_chrX_38556542_38693918 | TSPAN7 | chrX | 38556542 | 38693918 |
| a0001c0001t0001g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN7_chrX_38556542_38693918 | TSPAN7 | chrX | 38556542 | 38693918 |
| a0001c0001t0001g0024 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TSPAN7_chrX_38556542_38693918 | TSPAN7 | chrX | 38556542 | 38693918 |
| a0001c0001t0001g0025 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TSPAN7_chrX_38556542_38693918 | TSPAN7 | chrX | 38556542 | 38693918 |
| a0001c0001t0001g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN7_chrX_38556542_38693918 | TSPAN7 | chrX | 38556542 | 38693918 |
| a0001c0001t0001g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN7_chrX_38556542_38693918 | TSPAN7 | chrX | 38556542 | 38693918 |
| a0001c0001t0001g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN7_chrX_38556542_38693918 | TSPAN7 | chrX | 38556542 | 38693918 |
| a0001c0001t0001g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN7_chrX_38556542_38693918 | TSPAN7 | chrX | 38556542 | 38693918 |
| a0001c0001t0001g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN7_chrX_38556542_38693918 | TSPAN7 | chrX | 38556542 | 38693918 |
| a0001c0001t0001g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN7_chrX_38556542_38693918 | TSPAN7 | chrX | 38556542 | 38693918 |
| a0001c0001t0001g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN7_chrX_38556542_38693918 | TSPAN7 | chrX | 38556542 | 38693918 |
| a0001c0001t0001g0036 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN7_chrX_38556542_38693918 | TSPAN7 | chrX | 38556542 | 38693918 |
| a0001c0001t0001g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN7_chrX_38556542_38693918 | TSPAN7 | chrX | 38556542 | 38693918 |
| a0001c0001t0001g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN7_chrX_38556542_38693918 | TSPAN7 | chrX | 38556542 | 38693918 |
| a0001c0001t0001g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN7_chrX_38556542_38693918 | TSPAN7 | chrX | 38556542 | 38693918 |
| a0001c0001t0001g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN7_chrX_38556542_38693918 | TSPAN7 | chrX | 38556542 | 38693918 |
| a0001c0001t0001g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN7_chrX_38556542_38693918 | TSPAN7 | chrX | 38556542 | 38693918 |
| a0001c0001t0001g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN7_chrX_38556542_38693918 | TSPAN7 | chrX | 38556542 | 38693918 |
| a0001c0001t0001g0044 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN7_chrX_38556542_38693918 | TSPAN7 | chrX | 38556542 | 38693918 |
| a0001c0001t0001g0045 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TSPAN7_chrX_38556542_38693918 | TSPAN7 | chrX | 38556542 | 38693918 |
| a0001c0001t0001g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN7_chrX_38556542_38693918 | TSPAN7 | chrX | 38556542 | 38693918 |
| a0001c0001t0001g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN7_chrX_38556542_38693918 | TSPAN7 | chrX | 38556542 | 38693918 |
| a0001c0001t0001g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN7_chrX_38556542_38693918 | TSPAN7 | chrX | 38556542 | 38693918 |
| a0001c0001t0001g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN7_chrX_38556542_38693918 | TSPAN7 | chrX | 38556542 | 38693918 |
| a0001c0001t0001g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN7_chrX_38556542_38693918 | TSPAN7 | chrX | 38556542 | 38693918 |
| a0001c0001t0001g0051 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TSPAN7_chrX_38556542_38693918 | TSPAN7 | chrX | 38556542 | 38693918 |
| a0001c0001t0001g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN7_chrX_38556542_38693918 | TSPAN7 | chrX | 38556542 | 38693918 |
| a0001c0001t0001g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN7_chrX_38556542_38693918 | TSPAN7 | chrX | 38556542 | 38693918 |
| a0001c0001t0001g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN7_chrX_38556542_38693918 | TSPAN7 | chrX | 38556542 | 38693918 |
| a0001c0001t0001g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN7_chrX_38556542_38693918 | TSPAN7 | chrX | 38556542 | 38693918 |
| a0001c0001t0001g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN7_chrX_38556542_38693918 | TSPAN7 | chrX | 38556542 | 38693918 |
| a0001c0001t0001g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN7_chrX_38556542_38693918 | TSPAN7 | chrX | 38556542 | 38693918 |
| a0001c0001t0001g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN7_chrX_38556542_38693918 | TSPAN7 | chrX | 38556542 | 38693918 |
| a0001c0001t0001g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN7_chrX_38556542_38693918 | TSPAN7 | chrX | 38556542 | 38693918 |
| a0001c0001t0001g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN7_chrX_38556542_38693918 | TSPAN7 | chrX | 38556542 | 38693918 |
| a0001c0001t0001g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN7_chrX_38556542_38693918 | TSPAN7 | chrX | 38556542 | 38693918 |
| a0001c0001t0001g0070 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TSPAN7_chrX_38556542_38693918 | TSPAN7 | chrX | 38556542 | 38693918 |
| a0001c0001t0001g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN7_chrX_38556542_38693918 | TSPAN7 | chrX | 38556542 | 38693918 |
| a0001c0001t0001g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN7_chrX_38556542_38693918 | TSPAN7 | chrX | 38556542 | 38693918 |
| a0001c0001t0001g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN7_chrX_38556542_38693918 | TSPAN7 | chrX | 38556542 | 38693918 |
| a0001c0001t0001g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN7_chrX_38556542_38693918 | TSPAN7 | chrX | 38556542 | 38693918 |
| a0001c0001t0001g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN7_chrX_38556542_38693918 | TSPAN7 | chrX | 38556542 | 38693918 |
| a0001c0001t0001g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN7_chrX_38556542_38693918 | TSPAN7 | chrX | 38556542 | 38693918 |
| a0001c0001t0001g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN7_chrX_38556542_38693918 | TSPAN7 | chrX | 38556542 | 38693918 |
| a0001c0001t0001g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN7_chrX_38556542_38693918 | TSPAN7 | chrX | 38556542 | 38693918 |
| a0001c0001t0001g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN7_chrX_38556542_38693918 | TSPAN7 | chrX | 38556542 | 38693918 |
| a0001c0001t0001g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN7_chrX_38556542_38693918 | TSPAN7 | chrX | 38556542 | 38693918 |
| a0001c0001t0001g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN7_chrX_38556542_38693918 | TSPAN7 | chrX | 38556542 | 38693918 |
| a0001c0001t0001g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN7_chrX_38556542_38693918 | TSPAN7 | chrX | 38556542 | 38693918 |
| a0001c0001t0001g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN7_chrX_38556542_38693918 | TSPAN7 | chrX | 38556542 | 38693918 |
| a0001c0001t0001g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN7_chrX_38556542_38693918 | TSPAN7 | chrX | 38556542 | 38693918 |
| a0001c0001t0001g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN7_chrX_38556542_38693918 | TSPAN7 | chrX | 38556542 | 38693918 |
| a0001c0001t0001g0095 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TSPAN7_chrX_38556542_38693918 | TSPAN7 | chrX | 38556542 | 38693918 |
| a0001c0001t0001g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN7_chrX_38556542_38693918 | TSPAN7 | chrX | 38556542 | 38693918 |
| a0001c0001t0001g0098 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TSPAN7_chrX_38556542_38693918 | TSPAN7 | chrX | 38556542 | 38693918 |
| a0001c0001t0001g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN7_chrX_38556542_38693918 | TSPAN7 | chrX | 38556542 | 38693918 |
| a0001c0001t0001g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN7_chrX_38556542_38693918 | TSPAN7 | chrX | 38556542 | 38693918 |
| a0001c0001t0001g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN7_chrX_38556542_38693918 | TSPAN7 | chrX | 38556542 | 38693918 |
| a0001c0001t0001g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN7_chrX_38556542_38693918 | TSPAN7 | chrX | 38556542 | 38693918 |
| a0001c0001t0001g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN7_chrX_38556542_38693918 | TSPAN7 | chrX | 38556542 | 38693918 |
| a0001c0001t0001g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN7_chrX_38556542_38693918 | TSPAN7 | chrX | 38556542 | 38693918 |
| a0001c0001t0001g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN7_chrX_38556542_38693918 | TSPAN7 | chrX | 38556542 | 38693918 |
| a0001c0001t0001g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN7_chrX_38556542_38693918 | TSPAN7 | chrX | 38556542 | 38693918 |
| a0001c0001t0001g0108 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN7_chrX_38556542_38693918 | TSPAN7 | chrX | 38556542 | 38693918 |
| a0001c0001t0001g0110 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TSPAN7_chrX_38556542_38693918 | TSPAN7 | chrX | 38556542 | 38693918 |
| a0001c0001t0001g0111 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TSPAN7_chrX_38556542_38693918 | TSPAN7 | chrX | 38556542 | 38693918 |
| a0001c0001t0001g0112 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TSPAN7_chrX_38556542_38693918 | TSPAN7 | chrX | 38556542 | 38693918 |
| a0001c0001t0001g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN7_chrX_38556542_38693918 | TSPAN7 | chrX | 38556542 | 38693918 |
| a0001c0001t0001g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN7_chrX_38556542_38693918 | TSPAN7 | chrX | 38556542 | 38693918 |
| a0001c0001t0001g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN7_chrX_38556542_38693918 | TSPAN7 | chrX | 38556542 | 38693918 |
| a0001c0001t0001g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN7_chrX_38556542_38693918 | TSPAN7 | chrX | 38556542 | 38693918 |
| a0001c0001t0001g0118 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN7_chrX_38556542_38693918 | TSPAN7 | chrX | 38556542 | 38693918 |
| a0001c0001t0001g0119 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN7_chrX_38556542_38693918 | TSPAN7 | chrX | 38556542 | 38693918 |
| a0001c0001t0001g0120 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN7_chrX_38556542_38693918 | TSPAN7 | chrX | 38556542 | 38693918 |
| a0001c0001t0001g0121 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN7_chrX_38556542_38693918 | TSPAN7 | chrX | 38556542 | 38693918 |
| a0001c0001t0001g0122 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN7_chrX_38556542_38693918 | TSPAN7 | chrX | 38556542 | 38693918 |
| a0001c0001t0001g0123 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN7_chrX_38556542_38693918 | TSPAN7 | chrX | 38556542 | 38693918 |
| a0001c0001t0001g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN7_chrX_38556542_38693918 | TSPAN7 | chrX | 38556542 | 38693918 |
| a0001c0001t0001g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN7_chrX_38556542_38693918 | TSPAN7 | chrX | 38556542 | 38693918 |
| a0001c0001t0001g0129 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN7_chrX_38556542_38693918 | TSPAN7 | chrX | 38556542 | 38693918 |
| a0001c0001t0001g0131 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TSPAN7_chrX_38556542_38693918 | TSPAN7 | chrX | 38556542 | 38693918 |
| a0001c0001t0001g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN7_chrX_38556542_38693918 | TSPAN7 | chrX | 38556542 | 38693918 |
| a0001c0001t0001g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN7_chrX_38556542_38693918 | TSPAN7 | chrX | 38556542 | 38693918 |
| a0001c0001t0001g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN7_chrX_38556542_38693918 | TSPAN7 | chrX | 38556542 | 38693918 |
| a0001c0001t0001g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN7_chrX_38556542_38693918 | TSPAN7 | chrX | 38556542 | 38693918 |
| a0001c0001t0001g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN7_chrX_38556542_38693918 | TSPAN7 | chrX | 38556542 | 38693918 |
| a0001c0001t0001g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN7_chrX_38556542_38693918 | TSPAN7 | chrX | 38556542 | 38693918 |
| a0001c0001t0001g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN7_chrX_38556542_38693918 | TSPAN7 | chrX | 38556542 | 38693918 |
| a0001c0001t0001g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN7_chrX_38556542_38693918 | TSPAN7 | chrX | 38556542 | 38693918 |
| a0001c0001t0001g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN7_chrX_38556542_38693918 | TSPAN7 | chrX | 38556542 | 38693918 |
| a0001c0001t0001g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN7_chrX_38556542_38693918 | TSPAN7 | chrX | 38556542 | 38693918 |
| a0001c0001t0001g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN7_chrX_38556542_38693918 | TSPAN7 | chrX | 38556542 | 38693918 |
| a0001c0001t0001g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN7_chrX_38556542_38693918 | TSPAN7 | chrX | 38556542 | 38693918 |
| a0001c0001t0001g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN7_chrX_38556542_38693918 | TSPAN7 | chrX | 38556542 | 38693918 |
| a0001c0001t0001g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN7_chrX_38556542_38693918 | TSPAN7 | chrX | 38556542 | 38693918 |
| a0001c0001t0001g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN7_chrX_38556542_38693918 | TSPAN7 | chrX | 38556542 | 38693918 |
| a0001c0001t0001g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN7_chrX_38556542_38693918 | TSPAN7 | chrX | 38556542 | 38693918 |
| a0001c0001t0001g0153 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TSPAN7_chrX_38556542_38693918 | TSPAN7 | chrX | 38556542 | 38693918 |
| a0001c0001t0001g0154 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TSPAN7_chrX_38556542_38693918 | TSPAN7 | chrX | 38556542 | 38693918 |
| a0001c0001t0001g0156 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TSPAN7_chrX_38556542_38693918 | TSPAN7 | chrX | 38556542 | 38693918 |
| a0001c0001t0001g0158 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | TSPAN7_chrX_38556542_38693918 | TSPAN7 | chrX | 38556542 | 38693918 |
| a0001c0001t0001g0159 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TSPAN7_chrX_38556542_38693918 | TSPAN7 | chrX | 38556542 | 38693918 |
| a0001c0001t0001g0160 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TSPAN7_chrX_38556542_38693918 | TSPAN7 | chrX | 38556542 | 38693918 |
| a0001c0001t0001g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN7_chrX_38556542_38693918 | TSPAN7 | chrX | 38556542 | 38693918 |
| a0001c0001t0001g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN7_chrX_38556542_38693918 | TSPAN7 | chrX | 38556542 | 38693918 |
| a0001c0001t0001g0164 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN7_chrX_38556542_38693918 | TSPAN7 | chrX | 38556542 | 38693918 |
| a0001c0001t0001g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN7_chrX_38556542_38693918 | TSPAN7 | chrX | 38556542 | 38693918 |
| a0001c0001t0001g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN7_chrX_38556542_38693918 | TSPAN7 | chrX | 38556542 | 38693918 |
| a0001c0001t0001g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN7_chrX_38556542_38693918 | TSPAN7 | chrX | 38556542 | 38693918 |
| a0001c0001t0001g0170 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN7_chrX_38556542_38693918 | TSPAN7 | chrX | 38556542 | 38693918 |
| a0001c0001t0001g0171 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN7_chrX_38556542_38693918 | TSPAN7 | chrX | 38556542 | 38693918 |
| a0001c0001t0001g0174 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TSPAN7_chrX_38556542_38693918 | TSPAN7 | chrX | 38556542 | 38693918 |
| a0001c0001t0001g0175 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN7_chrX_38556542_38693918 | TSPAN7 | chrX | 38556542 | 38693918 |
| a0001c0001t0001g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN7_chrX_38556542_38693918 | TSPAN7 | chrX | 38556542 | 38693918 |
| a0001c0001t0001g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN7_chrX_38556542_38693918 | TSPAN7 | chrX | 38556542 | 38693918 |
| a0001c0001t0001g0178 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN7_chrX_38556542_38693918 | TSPAN7 | chrX | 38556542 | 38693918 |
| a0001c0001t0001g0180 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN7_chrX_38556542_38693918 | TSPAN7 | chrX | 38556542 | 38693918 |
| a0001c0001t0001g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN7_chrX_38556542_38693918 | TSPAN7 | chrX | 38556542 | 38693918 |
| a0001c0001t0001g0185 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TSPAN7_chrX_38556542_38693918 | TSPAN7 | chrX | 38556542 | 38693918 |
| a0001c0001t0001g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN7_chrX_38556542_38693918 | TSPAN7 | chrX | 38556542 | 38693918 |
| a0001c0001t0001g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN7_chrX_38556542_38693918 | TSPAN7 | chrX | 38556542 | 38693918 |
| a0001c0001t0001g0188 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TSPAN7_chrX_38556542_38693918 | TSPAN7 | chrX | 38556542 | 38693918 |
| a0001c0001t0001g0190 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TSPAN7_chrX_38556542_38693918 | TSPAN7 | chrX | 38556542 | 38693918 |
| a0001c0001t0001g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN7_chrX_38556542_38693918 | TSPAN7 | chrX | 38556542 | 38693918 |
| a0001c0001t0001g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN7_chrX_38556542_38693918 | TSPAN7 | chrX | 38556542 | 38693918 |
| a0001c0001t0001g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN7_chrX_38556542_38693918 | TSPAN7 | chrX | 38556542 | 38693918 |
| a0001c0001t0001g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN7_chrX_38556542_38693918 | TSPAN7 | chrX | 38556542 | 38693918 |
| a0001c0001t0001g0196 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TSPAN7_chrX_38556542_38693918 | TSPAN7 | chrX | 38556542 | 38693918 |
| a0001c0001t0001g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN7_chrX_38556542_38693918 | TSPAN7 | chrX | 38556542 | 38693918 |
| a0001c0001t0001g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN7_chrX_38556542_38693918 | TSPAN7 | chrX | 38556542 | 38693918 |
| a0001c0001t0001g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN7_chrX_38556542_38693918 | TSPAN7 | chrX | 38556542 | 38693918 |
| a0001c0001t0001g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN7_chrX_38556542_38693918 | TSPAN7 | chrX | 38556542 | 38693918 |
| a0001c0001t0001g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN7_chrX_38556542_38693918 | TSPAN7 | chrX | 38556542 | 38693918 |
| a0001c0001t0001g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN7_chrX_38556542_38693918 | TSPAN7 | chrX | 38556542 | 38693918 |
| a0001c0001t0001g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN7_chrX_38556542_38693918 | TSPAN7 | chrX | 38556542 | 38693918 |
| a0001c0001t0001g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN7_chrX_38556542_38693918 | TSPAN7 | chrX | 38556542 | 38693918 |
| a0001c0001t0001g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN7_chrX_38556542_38693918 | TSPAN7 | chrX | 38556542 | 38693918 |
| a0001c0001t0001g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN7_chrX_38556542_38693918 | TSPAN7 | chrX | 38556542 | 38693918 |
| a0001c0001t0002g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN7_chrX_38556542_38693918 | TSPAN7 | chrX | 38556542 | 38693918 |
| a0001c0001t0002g0016 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN7_chrX_38556542_38693918 | TSPAN7 | chrX | 38556542 | 38693918 |
| a0001c0001t0002g0017 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN7_chrX_38556542_38693918 | TSPAN7 | chrX | 38556542 | 38693918 |
| a0001c0001t0002g0018 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN7_chrX_38556542_38693918 | TSPAN7 | chrX | 38556542 | 38693918 |
| a0001c0001t0002g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN7_chrX_38556542_38693918 | TSPAN7 | chrX | 38556542 | 38693918 |
| a0001c0001t0002g0020 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN7_chrX_38556542_38693918 | TSPAN7 | chrX | 38556542 | 38693918 |
| a0001c0001t0002g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN7_chrX_38556542_38693918 | TSPAN7 | chrX | 38556542 | 38693918 |
| a0001c0001t0002g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN7_chrX_38556542_38693918 | TSPAN7 | chrX | 38556542 | 38693918 |
| a0001c0001t0002g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN7_chrX_38556542_38693918 | TSPAN7 | chrX | 38556542 | 38693918 |
| a0001c0001t0002g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN7_chrX_38556542_38693918 | TSPAN7 | chrX | 38556542 | 38693918 |
| a0001c0001t0002g0032 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TSPAN7_chrX_38556542_38693918 | TSPAN7 | chrX | 38556542 | 38693918 |
| a0001c0001t0002g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN7_chrX_38556542_38693918 | TSPAN7 | chrX | 38556542 | 38693918 |
| a0001c0001t0002g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN7_chrX_38556542_38693918 | TSPAN7 | chrX | 38556542 | 38693918 |
| a0001c0001t0002g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN7_chrX_38556542_38693918 | TSPAN7 | chrX | 38556542 | 38693918 |
| a0001c0001t0002g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN7_chrX_38556542_38693918 | TSPAN7 | chrX | 38556542 | 38693918 |
| a0001c0001t0002g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN7_chrX_38556542_38693918 | TSPAN7 | chrX | 38556542 | 38693918 |
| a0001c0001t0002g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN7_chrX_38556542_38693918 | TSPAN7 | chrX | 38556542 | 38693918 |
| a0001c0001t0002g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN7_chrX_38556542_38693918 | TSPAN7 | chrX | 38556542 | 38693918 |
| a0001c0001t0002g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN7_chrX_38556542_38693918 | TSPAN7 | chrX | 38556542 | 38693918 |
| a0001c0001t0002g0094 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TSPAN7_chrX_38556542_38693918 | TSPAN7 | chrX | 38556542 | 38693918 |
| a0001c0001t0002g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN7_chrX_38556542_38693918 | TSPAN7 | chrX | 38556542 | 38693918 |
| a0001c0001t0002g0102 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TSPAN7_chrX_38556542_38693918 | TSPAN7 | chrX | 38556542 | 38693918 |
| a0001c0001t0002g0109 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TSPAN7_chrX_38556542_38693918 | TSPAN7 | chrX | 38556542 | 38693918 |
| a0001c0001t0002g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN7_chrX_38556542_38693918 | TSPAN7 | chrX | 38556542 | 38693918 |
| a0001c0001t0002g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN7_chrX_38556542_38693918 | TSPAN7 | chrX | 38556542 | 38693918 |
| a0001c0001t0002g0126 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | TSPAN7_chrX_38556542_38693918 | TSPAN7 | chrX | 38556542 | 38693918 |
| a0001c0001t0002g0127 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TSPAN7_chrX_38556542_38693918 | TSPAN7 | chrX | 38556542 | 38693918 |
| a0001c0001t0002g0130 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TSPAN7_chrX_38556542_38693918 | TSPAN7 | chrX | 38556542 | 38693918 |
| a0001c0001t0002g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN7_chrX_38556542_38693918 | TSPAN7 | chrX | 38556542 | 38693918 |
| a0001c0001t0002g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN7_chrX_38556542_38693918 | TSPAN7 | chrX | 38556542 | 38693918 |
| a0001c0001t0002g0149 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TSPAN7_chrX_38556542_38693918 | TSPAN7 | chrX | 38556542 | 38693918 |
| a0001c0001t0002g0150 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN7_chrX_38556542_38693918 | TSPAN7 | chrX | 38556542 | 38693918 |
| a0001c0001t0002g0151 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN7_chrX_38556542_38693918 | TSPAN7 | chrX | 38556542 | 38693918 |
| a0001c0001t0002g0155 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN7_chrX_38556542_38693918 | TSPAN7 | chrX | 38556542 | 38693918 |
| a0001c0001t0002g0157 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TSPAN7_chrX_38556542_38693918 | TSPAN7 | chrX | 38556542 | 38693918 |
| a0001c0001t0002g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN7_chrX_38556542_38693918 | TSPAN7 | chrX | 38556542 | 38693918 |
| a0001c0001t0002g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN7_chrX_38556542_38693918 | TSPAN7 | chrX | 38556542 | 38693918 |
| a0001c0001t0002g0167 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN7_chrX_38556542_38693918 | TSPAN7 | chrX | 38556542 | 38693918 |
| a0001c0001t0002g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN7_chrX_38556542_38693918 | TSPAN7 | chrX | 38556542 | 38693918 |
| a0001c0001t0002g0179 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN7_chrX_38556542_38693918 | TSPAN7 | chrX | 38556542 | 38693918 |
| a0001c0001t0002g0182 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TSPAN7_chrX_38556542_38693918 | TSPAN7 | chrX | 38556542 | 38693918 |
| a0001c0001t0002g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN7_chrX_38556542_38693918 | TSPAN7 | chrX | 38556542 | 38693918 |
| a0001c0001t0002g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN7_chrX_38556542_38693918 | TSPAN7 | chrX | 38556542 | 38693918 |
| a0001c0001t0002g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN7_chrX_38556542_38693918 | TSPAN7 | chrX | 38556542 | 38693918 |
| a0001c0001t0002g0197 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TSPAN7_chrX_38556542_38693918 | TSPAN7 | chrX | 38556542 | 38693918 |
| a0001c0001t0002g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN7_chrX_38556542_38693918 | TSPAN7 | chrX | 38556542 | 38693918 |
| a0001c0001t0002g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN7_chrX_38556542_38693918 | TSPAN7 | chrX | 38556542 | 38693918 |
| a0001c0001t0003g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN7_chrX_38556542_38693918 | TSPAN7 | chrX | 38556542 | 38693918 |
| a0001c0001t0003g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN7_chrX_38556542_38693918 | TSPAN7 | chrX | 38556542 | 38693918 |
| a0001c0001t0003g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN7_chrX_38556542_38693918 | TSPAN7 | chrX | 38556542 | 38693918 |
| a0001c0001t0005g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN7_chrX_38556542_38693918 | TSPAN7 | chrX | 38556542 | 38693918 |
| a0001c0002t0001g0001 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TSPAN7_chrX_38556542_38693918 | TSPAN7 | chrX | 38556542 | 38693918 |
| a0001c0002t0001g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN7_chrX_38556542_38693918 | TSPAN7 | chrX | 38556542 | 38693918 |
| a0001c0002t0001g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN7_chrX_38556542_38693918 | TSPAN7 | chrX | 38556542 | 38693918 |
| a0001c0002t0001g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN7_chrX_38556542_38693918 | TSPAN7 | chrX | 38556542 | 38693918 |
| a0001c0002t0001g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN7_chrX_38556542_38693918 | TSPAN7 | chrX | 38556542 | 38693918 |
| a0001c0002t0001g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN7_chrX_38556542_38693918 | TSPAN7 | chrX | 38556542 | 38693918 |
| a0001c0002t0001g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN7_chrX_38556542_38693918 | TSPAN7 | chrX | 38556542 | 38693918 |
| a0001c0002t0001g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN7_chrX_38556542_38693918 | TSPAN7 | chrX | 38556542 | 38693918 |
| a0001c0003t0001g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN7_chrX_38556542_38693918 | TSPAN7 | chrX | 38556542 | 38693918 |
| a0001c0003t0001g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN7_chrX_38556542_38693918 | TSPAN7 | chrX | 38556542 | 38693918 |
| a0001c0003t0001g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN7_chrX_38556542_38693918 | TSPAN7 | chrX | 38556542 | 38693918 |
| a0001c0003t0001g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN7_chrX_38556542_38693918 | TSPAN7 | chrX | 38556542 | 38693918 |
| a0001c0003t0001g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN7_chrX_38556542_38693918 | TSPAN7 | chrX | 38556542 | 38693918 |
| a0001c0003t0004g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TSPAN7_chrX_38556542_38693918 | TSPAN7 | chrX | 38556542 | 38693918 |
| a0002c0004t0001g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TSPAN7_chrX_38556542_38693918 | TSPAN7 | chrX | 38556542 | 38693918 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0001 | g0153 | EUR | GBR | TSPAN7_chrX_38556542_38693918 | TSPAN7 | chrX | 38556542 | 38693918 |
| HG00099 | hp2 | a0001 | c0001 | t0002 | g0102 | EUR | GBR | TSPAN7_chrX_38556542_38693918 | TSPAN7 | chrX | 38556542 | 38693918 |
| HG00140 | hp1 | a0001 | c0001 | t0001 | g0159 | EUR | GBR | TSPAN7_chrX_38556542_38693918 | TSPAN7 | chrX | 38556542 | 38693918 |
| HG00280 | hp1 | a0001 | c0001 | t0001 | g0156 | EUR | FIN | TSPAN7_chrX_38556542_38693918 | TSPAN7 | chrX | 38556542 | 38693918 |
| HG00438 | hp1 | a0001 | c0001 | t0002 | g0117 | EAS | CHS | TSPAN7_chrX_38556542_38693918 | TSPAN7 | chrX | 38556542 | 38693918 |
| HG00438 | hp2 | a0001 | c0001 | t0001 | g0085 | EAS | CHS | TSPAN7_chrX_38556542_38693918 | TSPAN7 | chrX | 38556542 | 38693918 |
| HG00609 | hp1 | a0001 | c0001 | t0001 | g0194 | EAS | CHS | TSPAN7_chrX_38556542_38693918 | TSPAN7 | chrX | 38556542 | 38693918 |
| HG00621 | hp1 | a0001 | c0001 | t0001 | g0038 | EAS | CHS | TSPAN7_chrX_38556542_38693918 | TSPAN7 | chrX | 38556542 | 38693918 |
| HG00642 | hp1 | a0001 | c0001 | t0002 | g0197 | AMR | PUR | TSPAN7_chrX_38556542_38693918 | TSPAN7 | chrX | 38556542 | 38693918 |
| HG00673 | hp1 | a0001 | c0001 | t0001 | g0144 | EAS | CHS | TSPAN7_chrX_38556542_38693918 | TSPAN7 | chrX | 38556542 | 38693918 |
| HG00738 | hp1 | a0001 | c0001 | t0001 | g0171 | AMR | PUR | TSPAN7_chrX_38556542_38693918 | TSPAN7 | chrX | 38556542 | 38693918 |
| HG00741 | hp1 | a0001 | c0001 | t0001 | g0036 | AMR | PUR | TSPAN7_chrX_38556542_38693918 | TSPAN7 | chrX | 38556542 | 38693918 |
| HG00741 | hp2 | a0001 | c0001 | t0002 | g0150 | AMR | PUR | TSPAN7_chrX_38556542_38693918 | TSPAN7 | chrX | 38556542 | 38693918 |
| HG01069 | hp1 | a0001 | c0001 | t0001 | g0178 | AMR | PUR | TSPAN7_chrX_38556542_38693918 | TSPAN7 | chrX | 38556542 | 38693918 |
| HG01071 | hp1 | a0001 | c0001 | t0002 | g0179 | AMR | PUR | TSPAN7_chrX_38556542_38693918 | TSPAN7 | chrX | 38556542 | 38693918 |
| HG01071 | hp2 | a0001 | c0001 | t0001 | g0116 | AMR | PUR | TSPAN7_chrX_38556542_38693918 | TSPAN7 | chrX | 38556542 | 38693918 |
| HG01074 | hp1 | a0001 | c0001 | t0001 | g0011 | AMR | PUR | TSPAN7_chrX_38556542_38693918 | TSPAN7 | chrX | 38556542 | 38693918 |
| HG01099 | hp1 | a0001 | c0001 | t0002 | g0097 | AMR | PUR | TSPAN7_chrX_38556542_38693918 | TSPAN7 | chrX | 38556542 | 38693918 |
| HG01106 | hp1 | a0001 | c0001 | t0002 | g0155 | AMR | PUR | TSPAN7_chrX_38556542_38693918 | TSPAN7 | chrX | 38556542 | 38693918 |
| HG01109 | hp1 | a0001 | c0001 | t0001 | g0120 | AMR | PUR | TSPAN7_chrX_38556542_38693918 | TSPAN7 | chrX | 38556542 | 38693918 |
| HG01167 | hp1 | a0001 | c0001 | t0001 | g0129 | AMR | PUR | TSPAN7_chrX_38556542_38693918 | TSPAN7 | chrX | 38556542 | 38693918 |
| HG01169 | hp1 | a0001 | c0001 | t0001 | g0164 | AMR | PUR | TSPAN7_chrX_38556542_38693918 | TSPAN7 | chrX | 38556542 | 38693918 |
| HG01169 | hp2 | a0001 | c0001 | t0001 | g0010 | AMR | PUR | TSPAN7_chrX_38556542_38693918 | TSPAN7 | chrX | 38556542 | 38693918 |
| HG01175 | hp1 | a0001 | c0001 | t0001 | g0004 | AMR | PUR | TSPAN7_chrX_38556542_38693918 | TSPAN7 | chrX | 38556542 | 38693918 |
| HG01175 | hp2 | a0001 | c0001 | t0002 | g0167 | AMR | PUR | TSPAN7_chrX_38556542_38693918 | TSPAN7 | chrX | 38556542 | 38693918 |
| HG01192 | hp1 | a0001 | c0001 | t0001 | g0180 | AMR | PUR | TSPAN7_chrX_38556542_38693918 | TSPAN7 | chrX | 38556542 | 38693918 |
| HG01243 | hp1 | a0001 | c0001 | t0001 | g0108 | AMR | PUR | TSPAN7_chrX_38556542_38693918 | TSPAN7 | chrX | 38556542 | 38693918 |
| HG01255 | hp1 | a0001 | c0001 | t0001 | g0073 | AMR | CLM | TSPAN7_chrX_38556542_38693918 | TSPAN7 | chrX | 38556542 | 38693918 |
| HG01256 | hp1 | a0001 | c0001 | t0001 | g0121 | AMR | CLM | TSPAN7_chrX_38556542_38693918 | TSPAN7 | chrX | 38556542 | 38693918 |
| HG01257 | hp1 | a0001 | c0001 | t0001 | g0123 | AMR | CLM | TSPAN7_chrX_38556542_38693918 | TSPAN7 | chrX | 38556542 | 38693918 |
| HG01257 | hp2 | a0001 | c0001 | t0001 | g0006 | AMR | CLM | TSPAN7_chrX_38556542_38693918 | TSPAN7 | chrX | 38556542 | 38693918 |
| HG01258 | hp1 | a0001 | c0001 | t0001 | g0006 | AMR | CLM | TSPAN7_chrX_38556542_38693918 | TSPAN7 | chrX | 38556542 | 38693918 |
| HG01261 | hp1 | a0001 | c0001 | t0002 | g0151 | AMR | CLM | TSPAN7_chrX_38556542_38693918 | TSPAN7 | chrX | 38556542 | 38693918 |
| HG01358 | hp1 | a0001 | c0001 | t0001 | g0122 | AMR | CLM | TSPAN7_chrX_38556542_38693918 | TSPAN7 | chrX | 38556542 | 38693918 |
| HG01433 | hp1 | a0001 | c0001 | t0001 | g0170 | AMR | CLM | TSPAN7_chrX_38556542_38693918 | TSPAN7 | chrX | 38556542 | 38693918 |
| HG01515 | hp1 | a0001 | c0001 | t0002 | g0149 | EUR | IBS | TSPAN7_chrX_38556542_38693918 | TSPAN7 | chrX | 38556542 | 38693918 |
| HG01517 | hp1 | a0001 | c0001 | t0001 | g0095 | EUR | IBS | TSPAN7_chrX_38556542_38693918 | TSPAN7 | chrX | 38556542 | 38693918 |
| HG01517 | hp2 | a0001 | c0001 | t0002 | g0127 | EUR | IBS | TSPAN7_chrX_38556542_38693918 | TSPAN7 | chrX | 38556542 | 38693918 |
| HG01884 | hp1 | a0001 | c0001 | t0001 | g0187 | AFR | ACB | TSPAN7_chrX_38556542_38693918 | TSPAN7 | chrX | 38556542 | 38693918 |
| HG01884 | hp2 | a0001 | c0003 | t0001 | g0201 | AFR | ACB | TSPAN7_chrX_38556542_38693918 | TSPAN7 | chrX | 38556542 | 38693918 |
| HG01891 | hp1 | a0001 | c0001 | t0001 | g0152 | AFR | ACB | TSPAN7_chrX_38556542_38693918 | TSPAN7 | chrX | 38556542 | 38693918 |
| HG01891 | hp2 | a0001 | c0001 | t0001 | g0083 | AFR | ACB | TSPAN7_chrX_38556542_38693918 | TSPAN7 | chrX | 38556542 | 38693918 |
| HG01928 | hp1 | a0001 | c0001 | t0001 | g0012 | AMR | PEL | TSPAN7_chrX_38556542_38693918 | TSPAN7 | chrX | 38556542 | 38693918 |
| HG01934 | hp1 | a0001 | c0001 | t0001 | g0044 | AMR | PEL | TSPAN7_chrX_38556542_38693918 | TSPAN7 | chrX | 38556542 | 38693918 |
| HG01943 | hp1 | a0001 | c0001 | t0001 | g0004 | AMR | PEL | TSPAN7_chrX_38556542_38693918 | TSPAN7 | chrX | 38556542 | 38693918 |
| HG01952 | hp1 | a0001 | c0001 | t0001 | g0175 | AMR | PEL | TSPAN7_chrX_38556542_38693918 | TSPAN7 | chrX | 38556542 | 38693918 |
| HG01975 | hp1 | a0001 | c0001 | t0001 | g0009 | AMR | PEL | TSPAN7_chrX_38556542_38693918 | TSPAN7 | chrX | 38556542 | 38693918 |
| HG01975 | hp2 | a0001 | c0001 | t0001 | g0119 | AMR | PEL | TSPAN7_chrX_38556542_38693918 | TSPAN7 | chrX | 38556542 | 38693918 |
| HG01981 | hp1 | a0001 | c0001 | t0001 | g0003 | AMR | PEL | TSPAN7_chrX_38556542_38693918 | TSPAN7 | chrX | 38556542 | 38693918 |
| HG01981 | hp2 | a0001 | c0001 | t0001 | g0096 | AMR | PEL | TSPAN7_chrX_38556542_38693918 | TSPAN7 | chrX | 38556542 | 38693918 |
| HG01993 | hp1 | a0001 | c0001 | t0001 | g0118 | AMR | PEL | TSPAN7_chrX_38556542_38693918 | TSPAN7 | chrX | 38556542 | 38693918 |
| HG01993 | hp2 | a0001 | c0001 | t0001 | g0003 | AMR | PEL | TSPAN7_chrX_38556542_38693918 | TSPAN7 | chrX | 38556542 | 38693918 |
| HG02015 | hp1 | a0001 | c0001 | t0001 | g0136 | EAS | KHV | TSPAN7_chrX_38556542_38693918 | TSPAN7 | chrX | 38556542 | 38693918 |
| HG02027 | hp1 | a0001 | c0001 | t0001 | g0034 | EAS | KHV | TSPAN7_chrX_38556542_38693918 | TSPAN7 | chrX | 38556542 | 38693918 |
| HG02040 | hp1 | a0001 | c0001 | t0001 | g0050 | EAS | KHV | TSPAN7_chrX_38556542_38693918 | TSPAN7 | chrX | 38556542 | 38693918 |
| HG02055 | hp1 | a0001 | c0001 | t0001 | g0072 | AFR | ACB | TSPAN7_chrX_38556542_38693918 | TSPAN7 | chrX | 38556542 | 38693918 |
| HG02056 | hp1 | a0001 | c0001 | t0001 | g0029 | EAS | KHV | TSPAN7_chrX_38556542_38693918 | TSPAN7 | chrX | 38556542 | 38693918 |
| HG02071 | hp1 | a0001 | c0001 | t0001 | g0030 | EAS | KHV | TSPAN7_chrX_38556542_38693918 | TSPAN7 | chrX | 38556542 | 38693918 |
| HG02074 | hp1 | a0001 | c0001 | t0001 | g0040 | EAS | KHV | TSPAN7_chrX_38556542_38693918 | TSPAN7 | chrX | 38556542 | 38693918 |
| HG02083 | hp1 | a0001 | c0001 | t0001 | g0037 | EAS | KHV | TSPAN7_chrX_38556542_38693918 | TSPAN7 | chrX | 38556542 | 38693918 |
| HG02129 | hp1 | a0001 | c0001 | t0002 | g0031 | EAS | KHV | TSPAN7_chrX_38556542_38693918 | TSPAN7 | chrX | 38556542 | 38693918 |
| HG02132 | hp1 | a0001 | c0001 | t0001 | g0176 | EAS | KHV | TSPAN7_chrX_38556542_38693918 | TSPAN7 | chrX | 38556542 | 38693918 |
| HG02135 | hp1 | a0001 | c0001 | t0001 | g0140 | EAS | KHV | TSPAN7_chrX_38556542_38693918 | TSPAN7 | chrX | 38556542 | 38693918 |
| HG02145 | hp1 | a0001 | c0001 | t0001 | g0205 | AFR | ACB | TSPAN7_chrX_38556542_38693918 | TSPAN7 | chrX | 38556542 | 38693918 |
| HG02257 | hp1 | a0001 | c0001 | t0002 | g0065 | AFR | ACB | TSPAN7_chrX_38556542_38693918 | TSPAN7 | chrX | 38556542 | 38693918 |
| HG02257 | hp2 | a0001 | c0002 | t0001 | g0214 | AFR | ACB | TSPAN7_chrX_38556542_38693918 | TSPAN7 | chrX | 38556542 | 38693918 |
| HG02258 | hp1 | a0001 | c0003 | t0001 | g0215 | AFR | ACB | TSPAN7_chrX_38556542_38693918 | TSPAN7 | chrX | 38556542 | 38693918 |
| HG02572 | hp1 | a0001 | c0001 | t0001 | g0090 | AFR | GWD | TSPAN7_chrX_38556542_38693918 | TSPAN7 | chrX | 38556542 | 38693918 |
| HG02602 | hp1 | a0001 | c0001 | t0002 | g0109 | SAS | PJL | TSPAN7_chrX_38556542_38693918 | TSPAN7 | chrX | 38556542 | 38693918 |
| HG02615 | hp1 | a0001 | c0001 | t0001 | g0084 | AFR | GWD | TSPAN7_chrX_38556542_38693918 | TSPAN7 | chrX | 38556542 | 38693918 |
| HG02615 | hp2 | a0001 | c0001 | t0005 | g0078 | AFR | GWD | TSPAN7_chrX_38556542_38693918 | TSPAN7 | chrX | 38556542 | 38693918 |
| HG02622 | hp1 | a0001 | c0003 | t0001 | g0181 | AFR | GWD | TSPAN7_chrX_38556542_38693918 | TSPAN7 | chrX | 38556542 | 38693918 |
| HG02622 | hp2 | a0001 | c0001 | t0001 | g0055 | AFR | GWD | TSPAN7_chrX_38556542_38693918 | TSPAN7 | chrX | 38556542 | 38693918 |
| HG02630 | hp1 | a0001 | c0001 | t0001 | g0203 | AFR | GWD | TSPAN7_chrX_38556542_38693918 | TSPAN7 | chrX | 38556542 | 38693918 |
| HG02630 | hp2 | a0001 | c0001 | t0003 | g0079 | AFR | GWD | TSPAN7_chrX_38556542_38693918 | TSPAN7 | chrX | 38556542 | 38693918 |
| HG02647 | hp1 | a0001 | c0001 | t0001 | g0077 | AFR | GWD | TSPAN7_chrX_38556542_38693918 | TSPAN7 | chrX | 38556542 | 38693918 |
| HG02683 | hp1 | a0001 | c0001 | t0001 | g0070 | SAS | PJL | TSPAN7_chrX_38556542_38693918 | TSPAN7 | chrX | 38556542 | 38693918 |
| HG02683 | hp2 | a0001 | c0001 | t0001 | g0160 | SAS | PJL | TSPAN7_chrX_38556542_38693918 | TSPAN7 | chrX | 38556542 | 38693918 |
| HG02698 | hp1 | a0001 | c0001 | t0002 | g0094 | SAS | PJL | TSPAN7_chrX_38556542_38693918 | TSPAN7 | chrX | 38556542 | 38693918 |
| HG02717 | hp1 | a0001 | c0002 | t0001 | g0074 | AFR | GWD | TSPAN7_chrX_38556542_38693918 | TSPAN7 | chrX | 38556542 | 38693918 |
| HG02723 | hp1 | a0001 | c0001 | t0001 | g0211 | AFR | GWD | TSPAN7_chrX_38556542_38693918 | TSPAN7 | chrX | 38556542 | 38693918 |
| HG02723 | hp2 | a0001 | c0001 | t0001 | g0061 | AFR | GWD | TSPAN7_chrX_38556542_38693918 | TSPAN7 | chrX | 38556542 | 38693918 |
| HG02735 | hp1 | a0001 | c0001 | t0001 | g0154 | SAS | PJL | TSPAN7_chrX_38556542_38693918 | TSPAN7 | chrX | 38556542 | 38693918 |
| HG02738 | hp1 | a0001 | c0001 | t0001 | g0196 | SAS | PJL | TSPAN7_chrX_38556542_38693918 | TSPAN7 | chrX | 38556542 | 38693918 |
| HG02809 | hp1 | a0001 | c0001 | t0001 | g0063 | AFR | GWD | TSPAN7_chrX_38556542_38693918 | TSPAN7 | chrX | 38556542 | 38693918 |
| HG02809 | hp2 | a0001 | c0001 | t0002 | g0022 | AFR | GWD | TSPAN7_chrX_38556542_38693918 | TSPAN7 | chrX | 38556542 | 38693918 |
| HG02818 | hp1 | a0001 | c0002 | t0001 | g0088 | AFR | GWD | TSPAN7_chrX_38556542_38693918 | TSPAN7 | chrX | 38556542 | 38693918 |
| HG02818 | hp2 | a0001 | c0001 | t0002 | g0208 | AFR | GWD | TSPAN7_chrX_38556542_38693918 | TSPAN7 | chrX | 38556542 | 38693918 |
| HG02895 | hp1 | a0001 | c0001 | t0001 | g0071 | AFR | GWD | TSPAN7_chrX_38556542_38693918 | TSPAN7 | chrX | 38556542 | 38693918 |
| HG02896 | hp1 | a0001 | c0001 | t0002 | g0069 | AFR | GWD | TSPAN7_chrX_38556542_38693918 | TSPAN7 | chrX | 38556542 | 38693918 |
| HG02896 | hp2 | a0001 | c0001 | t0001 | g0064 | AFR | GWD | TSPAN7_chrX_38556542_38693918 | TSPAN7 | chrX | 38556542 | 38693918 |
| HG02922 | hp1 | a0001 | c0001 | t0002 | g0191 | AFR | ESN | TSPAN7_chrX_38556542_38693918 | TSPAN7 | chrX | 38556542 | 38693918 |
| HG02922 | hp2 | a0001 | c0001 | t0001 | g0060 | AFR | ESN | TSPAN7_chrX_38556542_38693918 | TSPAN7 | chrX | 38556542 | 38693918 |
| HG02965 | hp1 | a0001 | c0003 | t0001 | g0066 | AFR | ESN | TSPAN7_chrX_38556542_38693918 | TSPAN7 | chrX | 38556542 | 38693918 |
| HG02976 | hp1 | a0001 | c0001 | t0003 | g0058 | AFR | ESN | TSPAN7_chrX_38556542_38693918 | TSPAN7 | chrX | 38556542 | 38693918 |
| HG02976 | hp2 | a0001 | c0001 | t0002 | g0028 | AFR | ESN | TSPAN7_chrX_38556542_38693918 | TSPAN7 | chrX | 38556542 | 38693918 |
| HG03017 | hp1 | a0001 | c0001 | t0001 | g0015 | SAS | PJL | TSPAN7_chrX_38556542_38693918 | TSPAN7 | chrX | 38556542 | 38693918 |
| HG03098 | hp1 | a0001 | c0001 | t0001 | g0082 | AFR | MSL | TSPAN7_chrX_38556542_38693918 | TSPAN7 | chrX | 38556542 | 38693918 |
| HG03130 | hp1 | a0001 | c0001 | t0001 | g0091 | AFR | ESN | TSPAN7_chrX_38556542_38693918 | TSPAN7 | chrX | 38556542 | 38693918 |
| HG03139 | hp1 | a0001 | c0001 | t0003 | g0057 | AFR | ESN | TSPAN7_chrX_38556542_38693918 | TSPAN7 | chrX | 38556542 | 38693918 |
| HG03195 | hp1 | a0001 | c0002 | t0001 | g0001 | AFR | ESN | TSPAN7_chrX_38556542_38693918 | TSPAN7 | chrX | 38556542 | 38693918 |
| HG03195 | hp2 | a0001 | c0002 | t0001 | g0213 | AFR | ESN | TSPAN7_chrX_38556542_38693918 | TSPAN7 | chrX | 38556542 | 38693918 |
| HG03209 | hp1 | a0001 | c0001 | t0002 | g0081 | AFR | MSL | TSPAN7_chrX_38556542_38693918 | TSPAN7 | chrX | 38556542 | 38693918 |
| HG03225 | hp1 | a0001 | c0001 | t0002 | g0013 | AFR | MSL | TSPAN7_chrX_38556542_38693918 | TSPAN7 | chrX | 38556542 | 38693918 |
| HG03486 | hp1 | a0001 | c0001 | t0001 | g0056 | AFR | MSL | TSPAN7_chrX_38556542_38693918 | TSPAN7 | chrX | 38556542 | 38693918 |
| HG03486 | hp2 | a0001 | c0001 | t0002 | g0076 | AFR | MSL | TSPAN7_chrX_38556542_38693918 | TSPAN7 | chrX | 38556542 | 38693918 |
| HG03490 | hp1 | a0001 | c0001 | t0001 | g0005 | SAS | PJL | TSPAN7_chrX_38556542_38693918 | TSPAN7 | chrX | 38556542 | 38693918 |
| HG03491 | hp1 | a0001 | c0001 | t0001 | g0005 | SAS | PJL | TSPAN7_chrX_38556542_38693918 | TSPAN7 | chrX | 38556542 | 38693918 |
| HG03491 | hp2 | a0001 | c0001 | t0001 | g0111 | SAS | PJL | TSPAN7_chrX_38556542_38693918 | TSPAN7 | chrX | 38556542 | 38693918 |
| HG03492 | hp1 | a0001 | c0001 | t0001 | g0112 | SAS | PJL | TSPAN7_chrX_38556542_38693918 | TSPAN7 | chrX | 38556542 | 38693918 |
| HG03516 | hp1 | a0001 | c0001 | t0001 | g0099 | AFR | ESN | TSPAN7_chrX_38556542_38693918 | TSPAN7 | chrX | 38556542 | 38693918 |
| HG03516 | hp2 | a0001 | c0002 | t0001 | g0068 | AFR | ESN | TSPAN7_chrX_38556542_38693918 | TSPAN7 | chrX | 38556542 | 38693918 |
| HG03540 | hp1 | a0001 | c0001 | t0001 | g0206 | AFR | GWD | TSPAN7_chrX_38556542_38693918 | TSPAN7 | chrX | 38556542 | 38693918 |
| HG03540 | hp2 | a0001 | c0001 | t0001 | g0023 | AFR | GWD | TSPAN7_chrX_38556542_38693918 | TSPAN7 | chrX | 38556542 | 38693918 |
| HG03579 | hp1 | a0001 | c0001 | t0002 | g0067 | AFR | MSL | TSPAN7_chrX_38556542_38693918 | TSPAN7 | chrX | 38556542 | 38693918 |
| HG03654 | hp1 | a0001 | c0001 | t0001 | g0051 | SAS | PJL | TSPAN7_chrX_38556542_38693918 | TSPAN7 | chrX | 38556542 | 38693918 |
| HG03688 | hp1 | a0001 | c0001 | t0001 | g0024 | SAS | STU | TSPAN7_chrX_38556542_38693918 | TSPAN7 | chrX | 38556542 | 38693918 |
| HG03704 | hp1 | a0001 | c0001 | t0002 | g0130 | SAS | PJL | TSPAN7_chrX_38556542_38693918 | TSPAN7 | chrX | 38556542 | 38693918 |
| HG03704 | hp2 | a0001 | c0001 | t0001 | g0098 | SAS | PJL | TSPAN7_chrX_38556542_38693918 | TSPAN7 | chrX | 38556542 | 38693918 |
| HG03710 | hp1 | a0001 | c0001 | t0002 | g0157 | SAS | PJL | TSPAN7_chrX_38556542_38693918 | TSPAN7 | chrX | 38556542 | 38693918 |
| HG03831 | hp1 | a0001 | c0001 | t0002 | g0032 | SAS | BEB | TSPAN7_chrX_38556542_38693918 | TSPAN7 | chrX | 38556542 | 38693918 |
| HG03831 | hp2 | a0001 | c0001 | t0001 | g0174 | SAS | BEB | TSPAN7_chrX_38556542_38693918 | TSPAN7 | chrX | 38556542 | 38693918 |
| HG03942 | hp1 | a0001 | c0001 | t0001 | g0045 | SAS | BEB | TSPAN7_chrX_38556542_38693918 | TSPAN7 | chrX | 38556542 | 38693918 |
| HG04115 | hp1 | a0001 | c0001 | t0002 | g0182 | SAS | STU | TSPAN7_chrX_38556542_38693918 | TSPAN7 | chrX | 38556542 | 38693918 |
| HG04199 | hp1 | a0001 | c0001 | t0001 | g0188 | SAS | STU | TSPAN7_chrX_38556542_38693918 | TSPAN7 | chrX | 38556542 | 38693918 |
| HG04204 | hp1 | a0001 | c0001 | t0001 | g0025 | SAS | STU | TSPAN7_chrX_38556542_38693918 | TSPAN7 | chrX | 38556542 | 38693918 |
| HG04228 | hp1 | a0001 | c0001 | t0001 | g0185 | SAS | STU | TSPAN7_chrX_38556542_38693918 | TSPAN7 | chrX | 38556542 | 38693918 |
| NA18522 | hp1 | a0001 | c0002 | t0001 | g0092 | AFR | YRI | TSPAN7_chrX_38556542_38693918 | TSPAN7 | chrX | 38556542 | 38693918 |
| NA18612 | hp1 | a0001 | c0001 | t0001 | g0093 | EAS | CHB | TSPAN7_chrX_38556542_38693918 | TSPAN7 | chrX | 38556542 | 38693918 |
| NA18747 | hp1 | a0001 | c0001 | t0001 | g0053 | EAS | CHB | TSPAN7_chrX_38556542_38693918 | TSPAN7 | chrX | 38556542 | 38693918 |
| NA18906 | hp1 | a0001 | c0001 | t0002 | g0080 | AFR | YRI | TSPAN7_chrX_38556542_38693918 | TSPAN7 | chrX | 38556542 | 38693918 |
| NA18906 | hp2 | a0001 | c0001 | t0001 | g0087 | AFR | YRI | TSPAN7_chrX_38556542_38693918 | TSPAN7 | chrX | 38556542 | 38693918 |
| NA18940 | hp1 | a0001 | c0001 | t0001 | g0115 | EAS | JPT | TSPAN7_chrX_38556542_38693918 | TSPAN7 | chrX | 38556542 | 38693918 |
| NA18942 | hp1 | a0001 | c0001 | t0001 | g0132 | EAS | JPT | TSPAN7_chrX_38556542_38693918 | TSPAN7 | chrX | 38556542 | 38693918 |
| NA18942 | hp2 | a0001 | c0001 | t0002 | g0052 | EAS | JPT | TSPAN7_chrX_38556542_38693918 | TSPAN7 | chrX | 38556542 | 38693918 |
| NA18943 | hp1 | a0001 | c0001 | t0002 | g0124 | EAS | JPT | TSPAN7_chrX_38556542_38693918 | TSPAN7 | chrX | 38556542 | 38693918 |
| NA18944 | hp1 | a0001 | c0001 | t0001 | g0086 | EAS | JPT | TSPAN7_chrX_38556542_38693918 | TSPAN7 | chrX | 38556542 | 38693918 |
| NA18945 | hp1 | a0001 | c0001 | t0001 | g0114 | EAS | JPT | TSPAN7_chrX_38556542_38693918 | TSPAN7 | chrX | 38556542 | 38693918 |
| NA18948 | hp1 | a0001 | c0001 | t0002 | g0017 | EAS | JPT | TSPAN7_chrX_38556542_38693918 | TSPAN7 | chrX | 38556542 | 38693918 |
| NA18952 | hp1 | a0001 | c0001 | t0001 | g0046 | EAS | JPT | TSPAN7_chrX_38556542_38693918 | TSPAN7 | chrX | 38556542 | 38693918 |
| NA18953 | hp1 | a0001 | c0001 | t0001 | g0105 | EAS | JPT | TSPAN7_chrX_38556542_38693918 | TSPAN7 | chrX | 38556542 | 38693918 |
| NA18959 | hp1 | a0001 | c0001 | t0001 | g0146 | EAS | JPT | TSPAN7_chrX_38556542_38693918 | TSPAN7 | chrX | 38556542 | 38693918 |
| NA18960 | hp1 | a0001 | c0001 | t0001 | g0163 | EAS | JPT | TSPAN7_chrX_38556542_38693918 | TSPAN7 | chrX | 38556542 | 38693918 |
| NA18961 | hp1 | a0001 | c0001 | t0001 | g0048 | EAS | JPT | TSPAN7_chrX_38556542_38693918 | TSPAN7 | chrX | 38556542 | 38693918 |
| NA18962 | hp1 | a0001 | c0001 | t0001 | g0106 | EAS | JPT | TSPAN7_chrX_38556542_38693918 | TSPAN7 | chrX | 38556542 | 38693918 |
| NA18963 | hp1 | a0001 | c0001 | t0001 | g0027 | EAS | JPT | TSPAN7_chrX_38556542_38693918 | TSPAN7 | chrX | 38556542 | 38693918 |
| NA18963 | hp2 | a0001 | c0001 | t0001 | g0047 | EAS | JPT | TSPAN7_chrX_38556542_38693918 | TSPAN7 | chrX | 38556542 | 38693918 |
| NA18965 | hp1 | a0001 | c0001 | t0001 | g0193 | EAS | JPT | TSPAN7_chrX_38556542_38693918 | TSPAN7 | chrX | 38556542 | 38693918 |
| NA18966 | hp1 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | TSPAN7_chrX_38556542_38693918 | TSPAN7 | chrX | 38556542 | 38693918 |
| NA18967 | hp1 | a0001 | c0001 | t0001 | g0166 | EAS | JPT | TSPAN7_chrX_38556542_38693918 | TSPAN7 | chrX | 38556542 | 38693918 |
| NA18970 | hp1 | a0001 | c0001 | t0001 | g0139 | EAS | JPT | TSPAN7_chrX_38556542_38693918 | TSPAN7 | chrX | 38556542 | 38693918 |
| NA18971 | hp1 | a0001 | c0001 | t0001 | g0137 | EAS | JPT | TSPAN7_chrX_38556542_38693918 | TSPAN7 | chrX | 38556542 | 38693918 |
| NA18974 | hp1 | a0001 | c0001 | t0001 | g0104 | EAS | JPT | TSPAN7_chrX_38556542_38693918 | TSPAN7 | chrX | 38556542 | 38693918 |
| NA18977 | hp1 | a0001 | c0001 | t0002 | g0016 | EAS | JPT | TSPAN7_chrX_38556542_38693918 | TSPAN7 | chrX | 38556542 | 38693918 |
| NA18982 | hp1 | a0001 | c0001 | t0001 | g0043 | EAS | JPT | TSPAN7_chrX_38556542_38693918 | TSPAN7 | chrX | 38556542 | 38693918 |
| NA18983 | hp1 | a0001 | c0001 | t0001 | g0141 | EAS | JPT | TSPAN7_chrX_38556542_38693918 | TSPAN7 | chrX | 38556542 | 38693918 |
| NA18984 | hp1 | a0001 | c0001 | t0001 | g0192 | EAS | JPT | TSPAN7_chrX_38556542_38693918 | TSPAN7 | chrX | 38556542 | 38693918 |
| NA18985 | hp1 | a0002 | c0004 | t0001 | g0173 | EAS | JPT | TSPAN7_chrX_38556542_38693918 | TSPAN7 | chrX | 38556542 | 38693918 |
| NA18986 | hp1 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | TSPAN7_chrX_38556542_38693918 | TSPAN7 | chrX | 38556542 | 38693918 |
| NA18988 | hp1 | a0001 | c0001 | t0001 | g0125 | EAS | JPT | TSPAN7_chrX_38556542_38693918 | TSPAN7 | chrX | 38556542 | 38693918 |
| NA18989 | hp1 | a0001 | c0001 | t0001 | g0198 | EAS | JPT | TSPAN7_chrX_38556542_38693918 | TSPAN7 | chrX | 38556542 | 38693918 |
| NA18990 | hp1 | a0001 | c0001 | t0002 | g0172 | EAS | JPT | TSPAN7_chrX_38556542_38693918 | TSPAN7 | chrX | 38556542 | 38693918 |
| NA18991 | hp1 | a0001 | c0001 | t0001 | g0054 | EAS | JPT | TSPAN7_chrX_38556542_38693918 | TSPAN7 | chrX | 38556542 | 38693918 |
| NA18991 | hp2 | a0001 | c0001 | t0001 | g0169 | EAS | JPT | TSPAN7_chrX_38556542_38693918 | TSPAN7 | chrX | 38556542 | 38693918 |
| NA18994 | hp1 | a0001 | c0001 | t0001 | g0113 | EAS | JPT | TSPAN7_chrX_38556542_38693918 | TSPAN7 | chrX | 38556542 | 38693918 |
| NA18995 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | TSPAN7_chrX_38556542_38693918 | TSPAN7 | chrX | 38556542 | 38693918 |
| NA18999 | hp1 | a0001 | c0001 | t0001 | g0049 | EAS | JPT | TSPAN7_chrX_38556542_38693918 | TSPAN7 | chrX | 38556542 | 38693918 |
| NA18999 | hp2 | a0001 | c0001 | t0002 | g0165 | EAS | JPT | TSPAN7_chrX_38556542_38693918 | TSPAN7 | chrX | 38556542 | 38693918 |
| NA19000 | hp1 | a0001 | c0001 | t0001 | g0103 | EAS | JPT | TSPAN7_chrX_38556542_38693918 | TSPAN7 | chrX | 38556542 | 38693918 |
| NA19002 | hp1 | a0001 | c0001 | t0002 | g0138 | EAS | JPT | TSPAN7_chrX_38556542_38693918 | TSPAN7 | chrX | 38556542 | 38693918 |
| NA19002 | hp2 | a0001 | c0001 | t0001 | g0039 | EAS | JPT | TSPAN7_chrX_38556542_38693918 | TSPAN7 | chrX | 38556542 | 38693918 |
| NA19003 | hp1 | a0001 | c0001 | t0001 | g0100 | EAS | JPT | TSPAN7_chrX_38556542_38693918 | TSPAN7 | chrX | 38556542 | 38693918 |
| NA19003 | hp2 | a0001 | c0001 | t0001 | g0195 | EAS | JPT | TSPAN7_chrX_38556542_38693918 | TSPAN7 | chrX | 38556542 | 38693918 |
| NA19004 | hp1 | a0001 | c0001 | t0001 | g0168 | EAS | JPT | TSPAN7_chrX_38556542_38693918 | TSPAN7 | chrX | 38556542 | 38693918 |
| NA19005 | hp1 | a0001 | c0001 | t0001 | g0162 | EAS | JPT | TSPAN7_chrX_38556542_38693918 | TSPAN7 | chrX | 38556542 | 38693918 |
| NA19006 | hp1 | a0001 | c0001 | t0001 | g0147 | EAS | JPT | TSPAN7_chrX_38556542_38693918 | TSPAN7 | chrX | 38556542 | 38693918 |
| NA19007 | hp1 | a0001 | c0001 | t0001 | g0033 | EAS | JPT | TSPAN7_chrX_38556542_38693918 | TSPAN7 | chrX | 38556542 | 38693918 |
| NA19009 | hp1 | a0001 | c0001 | t0001 | g0035 | EAS | JPT | TSPAN7_chrX_38556542_38693918 | TSPAN7 | chrX | 38556542 | 38693918 |
| NA19012 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | TSPAN7_chrX_38556542_38693918 | TSPAN7 | chrX | 38556542 | 38693918 |
| NA19030 | hp1 | a0001 | c0001 | t0001 | g0210 | AFR | LWK | TSPAN7_chrX_38556542_38693918 | TSPAN7 | chrX | 38556542 | 38693918 |
| NA19030 | hp2 | a0001 | c0001 | t0001 | g0089 | AFR | LWK | TSPAN7_chrX_38556542_38693918 | TSPAN7 | chrX | 38556542 | 38693918 |
| NA19043 | hp1 | a0001 | c0001 | t0001 | g0075 | AFR | LWK | TSPAN7_chrX_38556542_38693918 | TSPAN7 | chrX | 38556542 | 38693918 |
| NA19055 | hp1 | a0001 | c0001 | t0002 | g0020 | EAS | JPT | TSPAN7_chrX_38556542_38693918 | TSPAN7 | chrX | 38556542 | 38693918 |
| NA19056 | hp1 | a0001 | c0001 | t0001 | g0101 | EAS | JPT | TSPAN7_chrX_38556542_38693918 | TSPAN7 | chrX | 38556542 | 38693918 |
| NA19058 | hp1 | a0001 | c0001 | t0002 | g0042 | EAS | JPT | TSPAN7_chrX_38556542_38693918 | TSPAN7 | chrX | 38556542 | 38693918 |
| NA19060 | hp1 | a0001 | c0001 | t0001 | g0148 | EAS | JPT | TSPAN7_chrX_38556542_38693918 | TSPAN7 | chrX | 38556542 | 38693918 |
| NA19062 | hp1 | a0001 | c0001 | t0001 | g0145 | EAS | JPT | TSPAN7_chrX_38556542_38693918 | TSPAN7 | chrX | 38556542 | 38693918 |
| NA19063 | hp1 | a0001 | c0001 | t0001 | g0134 | EAS | JPT | TSPAN7_chrX_38556542_38693918 | TSPAN7 | chrX | 38556542 | 38693918 |
| NA19065 | hp1 | a0001 | c0001 | t0001 | g0041 | EAS | JPT | TSPAN7_chrX_38556542_38693918 | TSPAN7 | chrX | 38556542 | 38693918 |
| NA19065 | hp2 | a0001 | c0001 | t0002 | g0189 | EAS | JPT | TSPAN7_chrX_38556542_38693918 | TSPAN7 | chrX | 38556542 | 38693918 |
| NA19066 | hp1 | a0001 | c0001 | t0001 | g0142 | EAS | JPT | TSPAN7_chrX_38556542_38693918 | TSPAN7 | chrX | 38556542 | 38693918 |
| NA19067 | hp1 | a0001 | c0001 | t0002 | g0161 | EAS | JPT | TSPAN7_chrX_38556542_38693918 | TSPAN7 | chrX | 38556542 | 38693918 |
| NA19068 | hp1 | a0001 | c0001 | t0001 | g0128 | EAS | JPT | TSPAN7_chrX_38556542_38693918 | TSPAN7 | chrX | 38556542 | 38693918 |
| NA19070 | hp1 | a0001 | c0001 | t0002 | g0018 | EAS | JPT | TSPAN7_chrX_38556542_38693918 | TSPAN7 | chrX | 38556542 | 38693918 |
| NA19078 | hp1 | a0001 | c0001 | t0002 | g0133 | EAS | JPT | TSPAN7_chrX_38556542_38693918 | TSPAN7 | chrX | 38556542 | 38693918 |
| NA19078 | hp2 | a0001 | c0001 | t0001 | g0026 | EAS | JPT | TSPAN7_chrX_38556542_38693918 | TSPAN7 | chrX | 38556542 | 38693918 |
| NA19079 | hp1 | a0001 | c0001 | t0001 | g0143 | EAS | JPT | TSPAN7_chrX_38556542_38693918 | TSPAN7 | chrX | 38556542 | 38693918 |
| NA19082 | hp1 | a0001 | c0001 | t0001 | g0107 | EAS | JPT | TSPAN7_chrX_38556542_38693918 | TSPAN7 | chrX | 38556542 | 38693918 |
| NA19083 | hp1 | a0001 | c0001 | t0001 | g0014 | EAS | JPT | TSPAN7_chrX_38556542_38693918 | TSPAN7 | chrX | 38556542 | 38693918 |
| NA19085 | hp1 | a0001 | c0001 | t0001 | g0184 | EAS | JPT | TSPAN7_chrX_38556542_38693918 | TSPAN7 | chrX | 38556542 | 38693918 |
| NA19086 | hp1 | a0001 | c0001 | t0001 | g0216 | EAS | JPT | TSPAN7_chrX_38556542_38693918 | TSPAN7 | chrX | 38556542 | 38693918 |
| NA19087 | hp1 | a0001 | c0001 | t0001 | g0186 | EAS | JPT | TSPAN7_chrX_38556542_38693918 | TSPAN7 | chrX | 38556542 | 38693918 |
| NA19087 | hp2 | a0001 | c0001 | t0002 | g0019 | EAS | JPT | TSPAN7_chrX_38556542_38693918 | TSPAN7 | chrX | 38556542 | 38693918 |
| NA19088 | hp1 | a0001 | c0001 | t0001 | g0135 | EAS | JPT | TSPAN7_chrX_38556542_38693918 | TSPAN7 | chrX | 38556542 | 38693918 |
| NA19091 | hp1 | a0001 | c0001 | t0001 | g0177 | EAS | JPT | TSPAN7_chrX_38556542_38693918 | TSPAN7 | chrX | 38556542 | 38693918 |
| NA20129 | hp1 | a0001 | c0001 | t0001 | g0062 | AFR | ASW | TSPAN7_chrX_38556542_38693918 | TSPAN7 | chrX | 38556542 | 38693918 |
| NA20129 | hp2 | a0001 | c0002 | t0001 | g0212 | AFR | ASW | TSPAN7_chrX_38556542_38693918 | TSPAN7 | chrX | 38556542 | 38693918 |
| NA20752 | hp1 | a0001 | c0001 | t0001 | g0190 | EUR | TSI | TSPAN7_chrX_38556542_38693918 | TSPAN7 | chrX | 38556542 | 38693918 |
| NA20805 | hp1 | a0001 | c0001 | t0001 | g0110 | EUR | TSI | TSPAN7_chrX_38556542_38693918 | TSPAN7 | chrX | 38556542 | 38693918 |
| NA20905 | hp1 | a0001 | c0001 | t0001 | g0131 | SAS | GIH | TSPAN7_chrX_38556542_38693918 | TSPAN7 | chrX | 38556542 | 38693918 |
| HG02109 | hp1 | a0001 | c0001 | t0001 | g0204 | AFR | ACB | TSPAN7_chrX_38556542_38693918 | TSPAN7 | chrX | 38556542 | 38693918 |
| HG02109 | hp2 | a0001 | c0003 | t0004 | g0207 | AFR | ACB | TSPAN7_chrX_38556542_38693918 | TSPAN7 | chrX | 38556542 | 38693918 |
| HG02486 | hp1 | a0001 | c0001 | t0002 | g0183 | AFR | ACB | TSPAN7_chrX_38556542_38693918 | TSPAN7 | chrX | 38556542 | 38693918 |
| HG02559 | hp1 | a0001 | c0001 | t0001 | g0199 | AFR | ACB | TSPAN7_chrX_38556542_38693918 | TSPAN7 | chrX | 38556542 | 38693918 |
| HG02559 | hp2 | a0001 | c0002 | t0001 | g0001 | AFR | ACB | TSPAN7_chrX_38556542_38693918 | TSPAN7 | chrX | 38556542 | 38693918 |
| HG03471 | hp1 | a0001 | c0003 | t0001 | g0200 | AFR | MSL | TSPAN7_chrX_38556542_38693918 | TSPAN7 | chrX | 38556542 | 38693918 |
| HG06807 | hp1 | a0001 | c0001 | t0001 | g0059 | AFR | USA | TSPAN7_chrX_38556542_38693918 | TSPAN7 | chrX | 38556542 | 38693918 |
| HG06807 | hp2 | a0001 | c0001 | t0001 | g0202 | AFR | USA | TSPAN7_chrX_38556542_38693918 | TSPAN7 | chrX | 38556542 | 38693918 |
| NA18955 | hp1 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | TSPAN7_chrX_38556542_38693918 | TSPAN7 | chrX | 38556542 | 38693918 |
| NA21309 | hp1 | a0001 | c0001 | t0002 | g0021 | AFR | LWK | TSPAN7_chrX_38556542_38693918 | TSPAN7 | chrX | 38556542 | 38693918 |
| NA21309 | hp2 | a0001 | c0001 | t0002 | g0209 | AFR | LWK | TSPAN7_chrX_38556542_38693918 | TSPAN7 | chrX | 38556542 | 38693918 |
| homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0001 | g0158 | REF | REF | TSPAN7_chrX_38556542_38693918 | TSPAN7 | chrX | 38556542 | 38693918 |
| homoSapiens_grch38 | hp1 | a0001 | c0001 | t0002 | g0126 | REF | REF | TSPAN7_chrX_38556542_38693918 | TSPAN7 | chrX | 38556542 | 38693918 |
| 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:38681226
|
G | GT | 1 | a0002 | 1 | NA18985.hp1 | frameshift_variant | HIGH | c.623dupT | p.Met209fs | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 6/8 | 629/1742 | 624/750 | 208/249 | INFO_REALIGN_3_PRIME | chrX | 38681226 |
| 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:38666276
|
T | C | 1 | a0001c0002 | 9 | HG02257.hp2 HG02559.hp2 HG02717.hp1 others(6): Show |
synonymous_variant | LOW | c.237T>C | p.Ala79Ala | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 2/8 | 242/1742 | 237/750 | 79/249 | chrX | 38666276 | ||
| chrX:38674316
|
C | T | 1 | a0001c0003 | 6 | HG01884.hp2 HG02109.hp2 HG02258.hp1 others(3): Show |
splice_region_variant&synonymous_variant | LOW | c.441C>T | p.Ser147Ser | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 4/8 | 446/1742 | 441/750 | 147/249 | chrX | 38674316 |
| 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:38688001
|
A | G | 1 | a0001c0001t0005 | 1 | HG02615.hp2 | 3_prime_UTR_variant | MODIFIER | c.*70A>G | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 8/8 | 334 | chrX | 38688001 | |||||
| chrX:38688007
|
A | G | 1 | a0001c0001t0005 | 1 | HG02615.hp2 | 3_prime_UTR_variant | MODIFIER | c.*76A>G | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 8/8 | 340 | chrX | 38688007 | |||||
| chrX:38688054
|
C | A | 6 | a0001c0001t0001a0001c0001t0005a0001c0002t0001others(3): Show | 173 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(170): Show |
3_prime_UTR_variant | MODIFIER | c.*123C>A | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 8/8 | 387 | chrX | 38688054 | |||||
| chrX:38688197
|
A | C | 1 | a0001c0001t0005 | 1 | HG02615.hp2 | 3_prime_UTR_variant | MODIFIER | c.*266A>C | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 8/8 | 530 | chrX | 38688197 | |||||
| chrX:38688608
|
G | A | 7 | a0001c0001t0001a0001c0001t0003a0001c0001t0005others(4): Show | 176 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(173): Show |
3_prime_UTR_variant | MODIFIER | c.*677G>A | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 8/8 | 941 | chrX | 38688608 | |||||
| chrX:38688652
|
C | T | 1 | a0001c0003t0004 | 1 | HG02109.hp2 | 3_prime_UTR_variant | MODIFIER | c.*721C>T | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 8/8 | 985 | chrX | 38688652 | |||||
| chrX:38688829
|
G | A | 7 | a0001c0001t0001a0001c0001t0003a0001c0001t0005others(4): Show | 176 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(173): Show |
3_prime_UTR_variant | MODIFIER | c.*898G>A | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 8/8 | 1162 | chrX | 38688829 |
| 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:38561694
|
AAAG | A | 1 | a0001c0001t0001g0216 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.81+71_81+73delAAG | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 38561694 | |||||
| chrX:38561712
|
A | T | 2 | a0001c0002t0001g0214a0001c0003t0001g0215 | 2 | HG02257.hp2 HG02258.hp1 |
intron_variant | MODIFIER | c.81+85A>T | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38561712 | ||||||
| chrX:38561713
|
C | T | 4 | a0001c0001t0001g0210a0001c0001t0001g0211a0001c0002t0001g0212others(1): Show | 4 | HG02723.hp1 HG03195.hp2 NA19030.hp1 others(1): Show |
intron_variant | MODIFIER | c.81+86C>T | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38561713 | ||||||
| chrX:38561734
|
G | C | 82 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0010others(79): Show | 82 | HG00621.hp1 HG00741.hp1 HG01074.hp1 others(79): Show |
intron_variant | MODIFIER | c.81+107G>C | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38561734 | ||||||
| chrX:38561884
|
C | CA | 1 | a0001c0001t0001g0008 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.81+267dupA | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 38561884 | |||||
| chrX:38561884
|
CA | C | 8 | a0001c0001t0001g0082a0001c0001t0001g0083a0001c0001t0002g0080others(5): Show | 8 | HG01891.hp2 HG02257.hp2 HG02258.hp1 others(5): Show |
intron_variant | MODIFIER | c.81+267delA | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 38561884 | |||||
| chrX:38562069
|
C | T | 5 | a0001c0001t0001g0077a0001c0001t0001g0210a0001c0001t0001g0211others(2): Show | 5 | HG02647.hp1 HG02723.hp1 HG03195.hp2 others(2): Show |
intron_variant | MODIFIER | c.81+442C>T | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38562069 | ||||||
| chrX:38562102
|
T | C | 32 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0011others(29): Show | 32 | HG01074.hp1 HG01169.hp2 HG01891.hp2 others(29): Show |
intron_variant | MODIFIER | c.81+475T>C | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38562102 | ||||||
| chrX:38562113
|
G | A | 31 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0011others(28): Show | 31 | HG01074.hp1 HG01169.hp2 HG01891.hp2 others(28): Show |
intron_variant | MODIFIER | c.81+486G>A | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38562113 | ||||||
| chrX:38562176
|
T | C | 1 | a0001c0001t0001g0085 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.81+549T>C | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38562176 | ||||||
| chrX:38562242
|
A | G | 1 | a0001c0001t0002g0209 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.81+615A>G | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38562242 | ||||||
| chrX:38562355
|
A | G | 12 | a0001c0001t0001g0082a0001c0001t0001g0083a0001c0001t0001g0203others(9): Show | 12 | HG01891.hp2 HG02109.hp1 HG02109.hp2 others(9): Show |
intron_variant | MODIFIER | c.81+728A>G | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38562355 | ||||||
| chrX:38562454
|
T | C | 1 | a0001c0001t0002g0028 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.81+827T>C | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38562454 | ||||||
| chrX:38562550
|
G | T | 36 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0011others(33): Show | 36 | HG01074.hp1 HG01169.hp2 HG01884.hp2 others(33): Show |
intron_variant | MODIFIER | c.81+923G>T | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38562550 | ||||||
| chrX:38562556
|
G | GGGGGGAG others(8): Show |
1 | a0001c0001t0002g0197 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.81+947_81+961dupGG others(13): Show |
TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 38562556 | |||||
| chrX:38562556
|
GGGGGGAG others(8): Show |
G | 29 | a0001c0001t0001g0008a0001c0001t0001g0029a0001c0001t0001g0030others(26): Show | 29 | HG00621.hp1 HG00741.hp1 HG01934.hp1 others(26): Show |
intron_variant | MODIFIER | c.81+947_81+961delGG others(13): Show |
TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 38562556 | |||||
| chrX:38562558
|
G | GGGGAGGA | 6 | a0001c0001t0001g0203a0001c0001t0001g0204a0001c0001t0001g0205others(3): Show | 6 | HG02109.hp1 HG02109.hp2 HG02145.hp1 others(3): Show |
intron_variant | MODIFIER | c.81+934_81+940dupGA others(5): Show |
TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 38562558 | |||||
| chrX:38562571
|
A | AG | 2 | a0001c0001t0001g0198a0001c0001t0005g0078 | 2 | HG02615.hp2 NA18989.hp1 |
intron_variant | MODIFIER | c.81+949dupG | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 38562571 | |||||
| chrX:38562682
|
G | A | 28 | a0001c0001t0001g0008a0001c0001t0001g0029a0001c0001t0001g0030others(25): Show | 28 | HG00621.hp1 HG00741.hp1 HG01934.hp1 others(25): Show |
intron_variant | MODIFIER | c.81+1055G>A | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38562682 | ||||||
| chrX:38562757
|
G | T | 50 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0011others(47): Show | 50 | HG01074.hp1 HG01169.hp2 HG01255.hp1 others(47): Show |
intron_variant | MODIFIER | c.81+1130G>T | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38562757 | ||||||
| chrX:38562961
|
T | A | 54 | a0001c0001t0001g0008a0001c0001t0001g0029a0001c0001t0001g0030others(51): Show | 55 | HG00621.hp1 HG00741.hp1 HG01884.hp2 others(52): Show |
intron_variant | MODIFIER | c.81+1334T>A | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38562961 | ||||||
| chrX:38563284
|
TG | T | 1 | a0001c0001t0001g0009 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.81+1658delG | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38563284 | ||||||
| chrX:38563296
|
A | G | 47 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0011others(44): Show | 47 | HG01074.hp1 HG01169.hp2 HG01255.hp1 others(44): Show |
intron_variant | MODIFIER | c.81+1669A>G | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38563296 | ||||||
| chrX:38563329
|
G | T | 1 | a0001c0001t0001g0196 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.81+1702G>T | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38563329 | ||||||
| chrX:38563475
|
GGA | G | 9 | a0001c0001t0001g0082a0001c0001t0001g0083a0001c0001t0001g0203others(6): Show | 9 | HG01891.hp2 HG02109.hp1 HG02109.hp2 others(6): Show |
intron_variant | MODIFIER | c.81+1850_81+1851del others(2): Show |
TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 38563475 | |||||
| chrX:38563476
|
GA | G | 56 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0029others(53): Show | 57 | HG00609.hp1 HG00621.hp1 HG00741.hp1 others(54): Show |
intron_variant | MODIFIER | c.81+1850delA | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38563476 | ||||||
| chrX:38563477
|
A | G | 6 | a0001c0001t0001g0199a0001c0001t0001g0202a0001c0002t0001g0092others(3): Show | 6 | HG01884.hp2 HG02258.hp1 HG02559.hp1 others(3): Show |
intron_variant | MODIFIER | c.81+1850A>G | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38563477 | ||||||
| chrX:38563506
|
A | T | 1 | a0001c0002t0001g0214 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.81+1879A>T | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38563506 | ||||||
| chrX:38563764
|
A | T | 95 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(92): Show | 96 | HG00609.hp1 HG00621.hp1 HG00741.hp1 others(93): Show |
intron_variant | MODIFIER | c.81+2137A>T | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38563764 | ||||||
| chrX:38563808
|
G | A | 1 | a0001c0001t0001g0093 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.81+2181G>A | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38563808 | ||||||
| chrX:38563854
|
A | G | 1 | a0001c0001t0001g0027 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.81+2227A>G | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38563854 | ||||||
| chrX:38564124
|
C | T | 1 | a0001c0001t0001g0192 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.81+2497C>T | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38564124 | ||||||
| chrX:38564282
|
C | T | 1 | a0001c0001t0002g0191 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.81+2655C>T | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38564282 | ||||||
| chrX:38564431
|
G | A | 4 | a0001c0001t0001g0082a0001c0001t0001g0083a0001c0001t0002g0081others(1): Show | 4 | HG01891.hp2 HG02257.hp2 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.81+2804G>A | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38564431 | ||||||
| chrX:38564490
|
T | C | 61 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0029others(58): Show | 62 | HG00609.hp1 HG00621.hp1 HG00741.hp1 others(59): Show |
intron_variant | MODIFIER | c.81+2863T>C | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38564490 | ||||||
| chrX:38564763
|
T | C | 4 | a0001c0001t0001g0082a0001c0001t0001g0083a0001c0001t0002g0081others(1): Show | 4 | HG01891.hp2 HG02257.hp2 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.81+3136T>C | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38564763 | ||||||
| chrX:38564799
|
C | A | 1 | a0001c0001t0002g0094 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.81+3172C>A | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38564799 | ||||||
| chrX:38564978
|
C | G | 1 | a0001c0002t0001g0092 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.81+3351C>G | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38564978 | ||||||
| chrX:38564988
|
C | CT | 34 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0029others(31): Show | 35 | HG00609.hp1 HG00621.hp1 HG00741.hp1 others(32): Show |
intron_variant | MODIFIER | c.81+3370dupT | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 38564988 | |||||
| chrX:38564988
|
CT | C | 21 | a0001c0001t0001g0056a0001c0001t0001g0059a0001c0001t0001g0060others(18): Show | 21 | HG01255.hp1 HG02055.hp1 HG02257.hp1 others(18): Show |
intron_variant | MODIFIER | c.81+3370delT | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 38564988 | |||||
| chrX:38565221
|
C | CTTGT | 5 | a0001c0001t0001g0082a0001c0001t0001g0083a0001c0001t0001g0190others(2): Show | 5 | HG01891.hp2 HG02257.hp2 HG03098.hp1 others(2): Show |
intron_variant | MODIFIER | c.81+3616_81+3619dup others(4): Show |
TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 38565221 | |||||
| chrX:38565261
|
G | T | 4 | a0001c0001t0001g0082a0001c0001t0001g0083a0001c0001t0002g0081others(1): Show | 4 | HG01891.hp2 HG02257.hp2 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.81+3634G>T | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38565261 | ||||||
| chrX:38565299
|
A | G | 4 | a0001c0001t0001g0082a0001c0001t0001g0083a0001c0001t0002g0081others(1): Show | 4 | HG01891.hp2 HG02257.hp2 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.81+3672A>G | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38565299 | ||||||
| chrX:38565420
|
G | A | 61 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0029others(58): Show | 62 | HG00609.hp1 HG00621.hp1 HG00741.hp1 others(59): Show |
intron_variant | MODIFIER | c.81+3793G>A | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38565420 | ||||||
| chrX:38565421
|
G | T | 61 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0029others(58): Show | 62 | HG00609.hp1 HG00621.hp1 HG00741.hp1 others(59): Show |
intron_variant | MODIFIER | c.81+3794G>T | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38565421 | ||||||
| chrX:38565463
|
C | T | 1 | a0001c0001t0001g0054 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.81+3836C>T | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38565463 | ||||||
| chrX:38565825
|
T | C | 3 | a0001c0001t0001g0095a0001c0001t0001g0096a0001c0001t0002g0097 | 3 | HG01099.hp1 HG01517.hp1 HG01981.hp2 |
intron_variant | MODIFIER | c.81+4198T>C | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38565825 | ||||||
| chrX:38565886
|
G | A | 1 | a0001c0001t0005g0078 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.81+4259G>A | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38565886 | ||||||
| chrX:38566037
|
C | T | 2 | a0001c0001t0001g0202a0001c0003t0001g0201 | 2 | HG01884.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.81+4410C>T | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38566037 | ||||||
| chrX:38566101
|
T | C | 3 | a0001c0001t0001g0029a0001c0001t0001g0030a0001c0001t0002g0031 | 3 | HG02056.hp1 HG02071.hp1 HG02129.hp1 |
intron_variant | MODIFIER | c.81+4474T>C | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38566101 | ||||||
| chrX:38566298
|
C | T | 66 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0026others(63): Show | 67 | HG00609.hp1 HG00621.hp1 HG00741.hp1 others(64): Show |
intron_variant | MODIFIER | c.81+4671C>T | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38566298 | ||||||
| chrX:38566521
|
G | GT | 1 | a0001c0001t0001g0216 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.81+4901dupT | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 38566521 | |||||
| chrX:38566710
|
T | A | 1 | a0001c0001t0002g0209 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.81+5083T>A | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38566710 | ||||||
| chrX:38566724
|
TA | T | 1 | a0001c0001t0002g0189 | 1 | NA19065.hp2 | intron_variant | MODIFIER | c.81+5103delA | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 38566724 | |||||
| chrX:38566725
|
A | C | 1 | a0001c0001t0005g0078 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.81+5098A>C | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38566725 | ||||||
| chrX:38567092
|
A | AT | 26 | a0001c0001t0001g0055a0001c0001t0001g0087a0001c0001t0001g0089others(23): Show | 27 | HG01884.hp1 HG01884.hp2 HG02109.hp1 others(24): Show |
intron_variant | MODIFIER | c.81+5476dupT | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 38567092 | |||||
| chrX:38567092
|
A | ATT | 58 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(55): Show | 59 | HG00609.hp1 HG00621.hp1 HG00741.hp1 others(56): Show |
intron_variant | MODIFIER | c.81+5475_81+5476dup others(2): Show |
TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 38567092 | |||||
| chrX:38567294
|
G | A | 21 | a0001c0001t0001g0056a0001c0001t0001g0059a0001c0001t0001g0060others(18): Show | 21 | HG01255.hp1 HG02055.hp1 HG02257.hp1 others(18): Show |
intron_variant | MODIFIER | c.81+5667G>A | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38567294 | ||||||
| chrX:38567331
|
A | T | 1 | a0001c0001t0002g0031 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.81+5704A>T | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38567331 | ||||||
| chrX:38567355
|
G | A | 1 | a0001c0001t0001g0098 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.81+5728G>A | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38567355 | ||||||
| chrX:38567409
|
AGAC | A | 4 | a0001c0001t0001g0082a0001c0001t0001g0083a0001c0001t0002g0081others(1): Show | 4 | HG01891.hp2 HG02257.hp2 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.81+5783_81+5785del others(3): Show |
TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38567409 | ||||||
| chrX:38567796
|
T | C | 4 | a0001c0001t0001g0082a0001c0001t0001g0083a0001c0001t0002g0081others(1): Show | 4 | HG01891.hp2 HG02257.hp2 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.81+6169T>C | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38567796 | ||||||
| chrX:38567833
|
G | T | 52 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(49): Show | 53 | HG00609.hp1 HG00621.hp1 HG00741.hp1 others(50): Show |
intron_variant | MODIFIER | c.81+6206G>T | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38567833 | ||||||
| chrX:38568260
|
C | T | 1 | a0001c0001t0002g0028 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.81+6633C>T | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38568260 | ||||||
| chrX:38568296
|
G | GT | 4 | a0001c0001t0001g0053a0001c0001t0001g0199a0001c0001t0002g0183others(1): Show | 4 | HG02486.hp1 HG02559.hp1 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.81+6682dupT | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 38568296 | |||||
| chrX:38568296
|
GT | G | 24 | a0001c0001t0001g0056a0001c0001t0001g0059a0001c0001t0001g0060others(21): Show | 24 | HG01255.hp1 HG02055.hp1 HG02257.hp1 others(21): Show |
intron_variant | MODIFIER | c.81+6682delT | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 38568296 | |||||
| chrX:38568342
|
G | GA | 1 | a0001c0001t0001g0002 | 2 | NA18995.hp1 NA19012.hp1 |
intron_variant | MODIFIER | c.81+6721dupA | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 38568342 | |||||
| chrX:38568510
|
G | T | 1 | a0001c0001t0002g0028 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.81+6883G>T | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38568510 | ||||||
| chrX:38568652
|
T | C | 1 | a0001c0001t0002g0102 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.81+7025T>C | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38568652 | ||||||
| chrX:38568821
|
T | G | 5 | a0001c0001t0001g0103a0001c0001t0001g0104a0001c0001t0001g0105others(2): Show | 5 | NA18953.hp1 NA18962.hp1 NA18974.hp1 others(2): Show |
intron_variant | MODIFIER | c.81+7194T>G | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38568821 | ||||||
| chrX:38569118
|
G | A | 33 | a0001c0001t0001g0056a0001c0001t0001g0059a0001c0001t0001g0060others(30): Show | 33 | HG01255.hp1 HG01884.hp2 HG01891.hp2 others(30): Show |
intron_variant | MODIFIER | c.81+7491G>A | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38569118 | ||||||
| chrX:38569366
|
C | T | 4 | a0001c0001t0001g0082a0001c0001t0001g0083a0001c0001t0002g0081others(1): Show | 4 | HG01891.hp2 HG02257.hp2 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.81+7739C>T | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38569366 | ||||||
| chrX:38569435
|
G | A | 1 | a0001c0001t0001g0108 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.81+7808G>A | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38569435 | ||||||
| chrX:38569783
|
G | A | 97 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(94): Show | 98 | HG00609.hp1 HG00621.hp1 HG00741.hp1 others(95): Show |
intron_variant | MODIFIER | c.81+8156G>A | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38569783 | ||||||
| chrX:38570045
|
G | A | 2 | a0001c0001t0001g0108a0001c0001t0005g0078 | 2 | HG01243.hp1 HG02615.hp2 |
intron_variant | MODIFIER | c.81+8418G>A | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38570045 | ||||||
| chrX:38570279
|
C | T | 1 | a0001c0001t0001g0187 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.81+8652C>T | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38570279 | ||||||
| chrX:38570299
|
G | T | 1 | a0001c0001t0002g0052 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.81+8672G>T | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38570299 | ||||||
| chrX:38570333
|
C | T | 2 | a0001c0001t0001g0090a0001c0001t0001g0091 | 2 | HG02572.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.81+8706C>T | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38570333 | ||||||
| chrX:38570619
|
T | C | 2 | a0001c0001t0001g0110a0001c0001t0002g0109 | 2 | HG02602.hp1 NA20805.hp1 |
intron_variant | MODIFIER | c.81+8992T>C | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38570619 | ||||||
| chrX:38570685
|
A | C | 4 | a0001c0001t0001g0082a0001c0001t0001g0083a0001c0001t0002g0081others(1): Show | 4 | HG01891.hp2 HG02257.hp2 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.81+9058A>C | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38570685 | ||||||
| chrX:38570841
|
A | T | 2 | a0001c0002t0001g0212a0001c0002t0001g0213 | 2 | HG03195.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.81+9214A>T | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38570841 | ||||||
| chrX:38571058
|
T | C | 4 | a0001c0001t0001g0082a0001c0001t0001g0083a0001c0001t0002g0081others(1): Show | 4 | HG01891.hp2 HG02257.hp2 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.81+9431T>C | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38571058 | ||||||
| chrX:38571238
|
A | G | 9 | a0001c0001t0001g0006a0001c0001t0001g0178a0001c0001t0001g0180others(6): Show | 10 | HG00099.hp2 HG00642.hp1 HG01069.hp1 others(7): Show |
intron_variant | MODIFIER | c.81+9611A>G | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38571238 | ||||||
| chrX:38571266
|
T | C | 2 | a0001c0001t0001g0111a0001c0001t0001g0112 | 2 | HG03491.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.81+9639T>C | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38571266 | ||||||
| chrX:38571303
|
A | G | 1 | a0001c0002t0001g0092 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.81+9676A>G | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38571303 | ||||||
| chrX:38571345
|
C | T | 4 | a0001c0001t0001g0082a0001c0001t0001g0083a0001c0001t0002g0081others(1): Show | 4 | HG01891.hp2 HG02257.hp2 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.81+9718C>T | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38571345 | ||||||
| chrX:38571498
|
C | T | 2 | a0001c0002t0001g0212a0001c0002t0001g0213 | 2 | HG03195.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.81+9871C>T | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38571498 | ||||||
| chrX:38571743
|
T | TA | 11 | a0001c0001t0001g0082a0001c0001t0001g0083a0001c0001t0001g0199others(8): Show | 11 | HG01884.hp2 HG01891.hp2 HG02257.hp2 others(8): Show |
intron_variant | MODIFIER | c.81+10128dupA | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 38571743 | |||||
| chrX:38571743
|
TA | T | 5 | a0001c0001t0001g0023a0001c0001t0001g0084a0001c0001t0001g0210others(2): Show | 5 | HG02615.hp1 HG02723.hp1 HG03540.hp2 others(2): Show |
intron_variant | MODIFIER | c.81+10128delA | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 38571743 | |||||
| chrX:38571747
|
A | G | 2 | a0001c0001t0001g0024a0001c0001t0001g0025 | 2 | HG03688.hp1 HG04204.hp1 |
intron_variant | MODIFIER | c.81+10120A>G | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38571747 | ||||||
| chrX:38571871
|
A | C | 21 | a0001c0001t0001g0056a0001c0001t0001g0059a0001c0001t0001g0060others(18): Show | 21 | HG01255.hp1 HG02055.hp1 HG02257.hp1 others(18): Show |
intron_variant | MODIFIER | c.81+10244A>C | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38571871 | ||||||
| chrX:38572010
|
A | AT | 21 | a0001c0001t0001g0056a0001c0001t0001g0059a0001c0001t0001g0060others(18): Show | 21 | HG01255.hp1 HG02055.hp1 HG02257.hp1 others(18): Show |
intron_variant | MODIFIER | c.81+10391dupT | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 38572010 | |||||
| chrX:38572055
|
TTGTCAAA others(10): Show |
T | 29 | a0001c0001t0001g0056a0001c0001t0001g0059a0001c0001t0001g0060others(26): Show | 29 | HG01255.hp1 HG01884.hp2 HG02055.hp1 others(26): Show |
intron_variant | MODIFIER | c.81+10438_81+10454d others(19): Show |
TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 38572055 | |||||
| chrX:38572106
|
C | A | 4 | a0001c0001t0001g0082a0001c0001t0001g0083a0001c0001t0002g0081others(1): Show | 4 | HG01891.hp2 HG02257.hp2 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.81+10479C>A | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38572106 | ||||||
| chrX:38572624
|
TCAGTTCA others(562): Show |
T | 1 | a0001c0001t0002g0076 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.81+10998_81+11566d others(2): Show |
TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38572624 | ||||||
| chrX:38573194
|
A | T | 1 | a0001c0001t0002g0076 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.81+11567A>T | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38573194 | ||||||
| chrX:38573197
|
A | G | 1 | a0001c0001t0002g0076 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.81+11570A>G | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38573197 | ||||||
| chrX:38573198
|
A | G | 1 | a0001c0001t0002g0076 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.81+11571A>G | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38573198 | ||||||
| chrX:38573200
|
T | G | 1 | a0001c0001t0002g0076 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.81+11573T>G | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38573200 | ||||||
| chrX:38573203
|
G | A | 1 | a0001c0001t0002g0076 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.81+11576G>A | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38573203 | ||||||
| chrX:38573205
|
C | T | 1 | a0001c0001t0002g0076 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.81+11578C>T | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38573205 | ||||||
| chrX:38573338
|
A | G | 1 | a0001c0001t0001g0056 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.81+11711A>G | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38573338 | ||||||
| chrX:38573385
|
CACTT | C | 1 | a0001c0001t0002g0032 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.81+11761_81+11764d others(6): Show |
TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 38573385 | |||||
| chrX:38573571
|
C | T | 1 | a0001c0001t0001g0075 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.81+11944C>T | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38573571 | ||||||
| chrX:38573670
|
C | T | 1 | a0001c0001t0001g0177 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.81+12043C>T | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38573670 | ||||||
| chrX:38573850
|
A | AAGACCAC | 4 | a0001c0001t0001g0082a0001c0001t0001g0083a0001c0001t0002g0081others(1): Show | 4 | HG01891.hp2 HG02257.hp2 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.81+12227_81+12233d others(9): Show |
TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 38573850 | |||||
| chrX:38574005
|
C | T | 2 | a0001c0001t0002g0021a0001c0001t0002g0022 | 2 | HG02809.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.81+12378C>T | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38574005 | ||||||
| chrX:38574286
|
G | T | 1 | a0001c0001t0001g0051 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.81+12659G>T | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38574286 | ||||||
| chrX:38574299
|
CT | C | 3 | a0001c0001t0002g0076a0001c0001t0003g0057a0001c0001t0003g0058 | 3 | HG02976.hp1 HG03139.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.81+12677delT | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 38574299 | |||||
| chrX:38574413
|
CT | C | 1 | a0001c0001t0001g0113 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.81+12791delT | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 38574413 | |||||
| chrX:38574739
|
A | T | 99 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(96): Show | 100 | HG00609.hp1 HG00621.hp1 HG00741.hp1 others(97): Show |
intron_variant | MODIFIER | c.81+13112A>T | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38574739 | ||||||
| chrX:38574867
|
C | T | 58 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(55): Show | 59 | HG00609.hp1 HG00621.hp1 HG00741.hp1 others(56): Show |
intron_variant | MODIFIER | c.81+13240C>T | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38574867 | ||||||
| chrX:38575144
|
C | T | 1 | a0001c0001t0001g0175 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.81+13517C>T | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38575144 | ||||||
| chrX:38575559
|
T | C | 1 | a0001c0001t0001g0114 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.81+13932T>C | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38575559 | ||||||
| chrX:38575858
|
G | GT | 1 | a0001c0001t0001g0186 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.81+14234dupT | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 38575858 | |||||
| chrX:38576155
|
A | AG | 1 | a0001c0001t0002g0020 | 1 | NA19055.hp1 | intron_variant | MODIFIER | c.81+14529dupG | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 38576155 | |||||
| chrX:38576166
|
AC | A | 1 | a0001c0001t0001g0115 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.81+14542delC | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 38576166 | |||||
| chrX:38576443
|
A | AT | 1 | a0001c0001t0001g0115 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.81+14822dupT | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 38576443 | |||||
| chrX:38576601
|
G | A | 22 | a0001c0001t0001g0056a0001c0001t0001g0059a0001c0001t0001g0060others(19): Show | 22 | HG01255.hp1 HG02055.hp1 HG02132.hp1 others(19): Show |
intron_variant | MODIFIER | c.81+14974G>A | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38576601 | ||||||
| chrX:38576767
|
T | C | 34 | a0001c0001t0001g0056a0001c0001t0001g0059a0001c0001t0001g0060others(31): Show | 34 | HG01255.hp1 HG01884.hp2 HG01891.hp2 others(31): Show |
intron_variant | MODIFIER | c.81+15140T>C | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38576767 | ||||||
| chrX:38576769
|
G | A | 14 | a0001c0001t0001g0059a0001c0001t0001g0060a0001c0001t0001g0061others(11): Show | 14 | HG02257.hp1 HG02723.hp2 HG02809.hp1 others(11): Show |
intron_variant | MODIFIER | c.81+15142G>A | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38576769 | ||||||
| chrX:38576864
|
TG | T | 1 | a0001c0001t0001g0115 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.81+15239delG | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 38576864 | |||||
| chrX:38576870
|
G | A | 2 | a0001c0001t0001g0008a0001c0001t0001g0086 | 2 | NA18944.hp1 NA18955.hp1 |
intron_variant | MODIFIER | c.81+15243G>A | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38576870 | ||||||
| chrX:38577652
|
G | A | 1 | a0001c0001t0001g0108 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.81+16025G>A | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38577652 | ||||||
| chrX:38577668
|
T | TG | 1 | a0001c0001t0001g0115 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.81+16047dupG | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 38577668 | |||||
| chrX:38577675
|
A | AG | 1 | a0001c0001t0002g0182 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.81+16054dupG | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 38577675 | |||||
| chrX:38577719
|
T | C | 1 | a0001c0001t0001g0116 | 1 | HG01071.hp2 | intron_variant | MODIFIER | c.81+16092T>C | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38577719 | ||||||
| chrX:38577804
|
A | G | 1 | a0001c0001t0001g0083 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.81+16177A>G | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38577804 | ||||||
| chrX:38577810
|
T | TA | 4 | a0001c0001t0001g0087a0001c0001t0001g0187a0001c0002t0001g0001others(1): Show | 5 | HG01884.hp1 HG02559.hp2 HG02818.hp1 others(2): Show |
intron_variant | MODIFIER | c.81+16195dupA | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 38577810 | |||||
| chrX:38577812
|
A | T | 1 | a0001c0001t0001g0185 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.81+16185A>T | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38577812 | ||||||
| chrX:38577831
|
G | GT | 1 | a0001c0001t0001g0115 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.81+16206dupT | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 38577831 | |||||
| chrX:38577917
|
T | TC | 1 | a0001c0001t0002g0020 | 1 | NA19055.hp1 | intron_variant | MODIFIER | c.81+16292dupC | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 38577917 | |||||
| chrX:38578007
|
G | A | 1 | a0001c0001t0002g0117 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.81+16380G>A | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38578007 | ||||||
| chrX:38578085
|
TG | T | 1 | a0001c0001t0001g0115 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.81+16461delG | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 38578085 | |||||
| chrX:38578091
|
A | AT | 1 | a0001c0001t0002g0020 | 1 | NA19055.hp1 | intron_variant | MODIFIER | c.81+16465dupT | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 38578091 | |||||
| chrX:38578342
|
T | G | 2 | a0001c0001t0001g0199a0001c0003t0001g0200 | 2 | HG02559.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.81+16715T>G | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38578342 | ||||||
| chrX:38578391
|
T | G | 1 | a0001c0003t0001g0201 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.81+16764T>G | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38578391 | ||||||
| chrX:38578458
|
T | TA | 1 | a0001c0001t0001g0115 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.81+16832dupA | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 38578458 | |||||
| chrX:38578581
|
GC | G | 1 | a0001c0001t0001g0115 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.81+16956delC | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 38578581 | |||||
| chrX:38578600
|
C | T | 1 | a0001c0001t0001g0174 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.81+16973C>T | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38578600 | ||||||
| chrX:38578745
|
GA | G | 5 | a0001c0001t0001g0185a0001c0001t0001g0202a0001c0001t0002g0208others(2): Show | 5 | HG01884.hp2 HG02109.hp2 HG02818.hp2 others(2): Show |
intron_variant | MODIFIER | c.81+17125delA | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 38578745 | |||||
| chrX:38578773
|
T | TA | 1 | a0001c0001t0001g0115 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.81+17148dupA | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 38578773 | |||||
| chrX:38578853
|
AT | A | 1 | a0001c0001t0001g0115 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.81+17227delT | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38578853 | ||||||
| chrX:38578855
|
A | C | 1 | a0001c0001t0001g0115 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.81+17228A>C | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38578855 | ||||||
| chrX:38578858
|
C | T | 1 | a0001c0001t0001g0115 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.81+17231C>T | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38578858 | ||||||
| chrX:38578864
|
T | G | 1 | a0001c0001t0001g0115 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.81+17237T>G | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38578864 | ||||||
| chrX:38578865
|
G | T | 1 | a0001c0001t0001g0115 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.81+17238G>T | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38578865 | ||||||
| chrX:38578866
|
T | G | 1 | a0001c0001t0001g0115 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.81+17239T>G | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38578866 | ||||||
| chrX:38578867
|
A | G | 2 | a0001c0001t0002g0018a0001c0001t0002g0019 | 2 | NA19070.hp1 NA19087.hp2 |
intron_variant | MODIFIER | c.81+17240A>G | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38578867 | ||||||
| chrX:38578869
|
G | GT | 1 | a0001c0001t0001g0115 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.81+17242_81+17243i others(3): Show |
TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38578869 | ||||||
| chrX:38578870
|
G | T | 1 | a0001c0001t0001g0115 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.81+17243G>T | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38578870 | ||||||
| chrX:38578871
|
G | A | 1 | a0001c0001t0001g0115 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.81+17244G>A | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38578871 | ||||||
| chrX:38578920
|
G | T | 4 | a0001c0001t0001g0203a0001c0001t0001g0204a0001c0001t0001g0205others(1): Show | 4 | HG02109.hp1 HG02145.hp1 HG02630.hp1 others(1): Show |
intron_variant | MODIFIER | c.81+17293G>T | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38578920 | ||||||
| chrX:38578971
|
G | GA | 1 | a0001c0001t0001g0115 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.81+17348dupA | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 38578971 | |||||
| chrX:38578997
|
A | AG | 1 | a0002c0004t0001g0173 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.81+17375dupG | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 38578997 | |||||
| chrX:38579031
|
T | G | 1 | a0001c0002t0001g0214 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.81+17404T>G | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38579031 | ||||||
| chrX:38579134
|
G | GA | 1 | a0001c0001t0001g0115 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.81+17509dupA | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 38579134 | |||||
| chrX:38579176
|
AT | A | 1 | a0001c0001t0002g0020 | 1 | NA19055.hp1 | intron_variant | MODIFIER | c.81+17553delT | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 38579176 | |||||
| chrX:38579258
|
T | TA | 1 | a0001c0001t0002g0020 | 1 | NA19055.hp1 | intron_variant | MODIFIER | c.81+17633dupA | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 38579258 | |||||
| chrX:38579408
|
C | T | 8 | a0001c0001t0001g0082a0001c0001t0001g0083a0001c0001t0001g0199others(5): Show | 8 | HG01891.hp2 HG02257.hp2 HG02559.hp1 others(5): Show |
intron_variant | MODIFIER | c.81+17781C>T | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38579408 | ||||||
| chrX:38579417
|
T | TA | 5 | a0001c0001t0001g0084a0001c0001t0001g0118a0001c0001t0001g0210others(2): Show | 5 | HG01993.hp1 HG02615.hp1 HG02723.hp1 others(2): Show |
intron_variant | MODIFIER | c.81+17801dupA | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 38579417 | |||||
| chrX:38579429
|
T | A | 1 | a0001c0001t0001g0118 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.81+17802T>A | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38579429 | ||||||
| chrX:38579599
|
C | CA | 1 | a0001c0001t0001g0115 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.81+17975dupA | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 38579599 | |||||
| chrX:38579612
|
C | A | 1 | a0001c0001t0001g0196 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.81+17985C>A | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38579612 | ||||||
| chrX:38579697
|
A | AT | 1 | a0001c0001t0001g0115 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.81+18073dupT | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 38579697 | |||||
| chrX:38579761
|
T | A | 103 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(100): Show | 104 | HG00609.hp1 HG00621.hp1 HG00741.hp1 others(101): Show |
intron_variant | MODIFIER | c.81+18134T>A | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38579761 | ||||||
| chrX:38579823
|
G | GT | 1 | a0001c0001t0001g0115 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.81+18197dupT | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 38579823 | |||||
| chrX:38579849
|
A | C | 2 | a0001c0001t0002g0208a0001c0003t0004g0207 | 2 | HG02109.hp2 HG02818.hp2 |
intron_variant | MODIFIER | c.81+18222A>C | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38579849 | ||||||
| chrX:38579917
|
A | AT | 1 | a0001c0001t0001g0115 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.81+18295dupT | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 38579917 | |||||
| chrX:38580062
|
A | C | 4 | a0001c0001t0001g0203a0001c0001t0001g0204a0001c0001t0001g0205others(1): Show | 4 | HG02109.hp1 HG02145.hp1 HG02630.hp1 others(1): Show |
intron_variant | MODIFIER | c.81+18435A>C | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38580062 | ||||||
| chrX:38580206
|
T | C | 2 | a0001c0001t0001g0003a0001c0001t0001g0123 | 3 | HG01257.hp1 HG01981.hp1 HG01993.hp2 |
intron_variant | MODIFIER | c.81+18579T>C | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38580206 | ||||||
| chrX:38580354
|
G | A | 1 | a0001c0002t0001g0092 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.81+18727G>A | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38580354 | ||||||
| chrX:38580516
|
G | A | 10 | a0001c0001t0001g0055a0001c0001t0001g0087a0001c0001t0001g0089others(7): Show | 11 | HG01884.hp1 HG02559.hp2 HG02572.hp1 others(8): Show |
intron_variant | MODIFIER | c.81+18889G>A | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38580516 | ||||||
| chrX:38580825
|
C | T | 1 | a0001c0001t0002g0172 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.81+19198C>T | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38580825 | ||||||
| chrX:38581250
|
C | T | 4 | a0001c0001t0001g0203a0001c0001t0001g0204a0001c0001t0001g0205others(1): Show | 4 | HG02109.hp1 HG02145.hp1 HG02630.hp1 others(1): Show |
intron_variant | MODIFIER | c.81+19623C>T | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38581250 | ||||||
| chrX:38581487
|
G | A | 1 | a0001c0001t0002g0124 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.81+19860G>A | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38581487 | ||||||
| chrX:38581488
|
G | A | 1 | a0001c0001t0001g0125 | 1 | NA18988.hp1 | intron_variant | MODIFIER | c.81+19861G>A | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38581488 | ||||||
| chrX:38581500
|
C | A | 3 | a0001c0001t0001g0082a0001c0001t0001g0083a0001c0001t0002g0081 | 3 | HG01891.hp2 HG03098.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.81+19873C>A | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38581500 | ||||||
| chrX:38581543
|
A | G | 1 | a0001c0001t0001g0171 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.81+19916A>G | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38581543 | ||||||
| chrX:38581693
|
T | G | 2 | a0001c0001t0001g0199a0001c0003t0001g0200 | 2 | HG02559.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.81+20066T>G | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38581693 | ||||||
| chrX:38581743
|
A | G | 2 | a0001c0001t0002g0028a0001c0002t0001g0092 | 2 | HG02976.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.81+20116A>G | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38581743 | ||||||
| chrX:38581836
|
C | T | 4 | a0001c0001t0001g0119a0001c0001t0001g0120a0001c0001t0001g0121others(1): Show | 4 | HG01109.hp1 HG01256.hp1 HG01358.hp1 others(1): Show |
intron_variant | MODIFIER | c.81+20209C>T | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38581836 | ||||||
| chrX:38581989
|
C | T | 3 | a0001c0001t0001g0082a0001c0001t0001g0083a0001c0001t0002g0081 | 3 | HG01891.hp2 HG03098.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.81+20362C>T | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38581989 | ||||||
| chrX:38582051
|
T | C | 1 | a0001c0001t0002g0102 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.81+20424T>C | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38582051 | ||||||
| chrX:38582223
|
C | T | 1 | a0001c0001t0001g0170 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.81+20596C>T | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38582223 | ||||||
| chrX:38582279
|
A | G | 3 | a0001c0001t0001g0082a0001c0001t0001g0083a0001c0001t0002g0081 | 3 | HG01891.hp2 HG03098.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.81+20652A>G | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38582279 | ||||||
| chrX:38582294
|
T | C | 1 | a0001c0001t0001g0203 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.81+20667T>C | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38582294 | ||||||
| chrX:38582297
|
A | G | 7 | a0001c0001t0001g0087a0001c0001t0001g0089a0001c0001t0001g0090others(4): Show | 8 | HG01884.hp1 HG02559.hp2 HG02572.hp1 others(5): Show |
intron_variant | MODIFIER | c.81+20670A>G | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38582297 | ||||||
| chrX:38582346
|
T | TTTC | 1 | a0001c0001t0001g0169 | 1 | NA18991.hp2 | intron_variant | MODIFIER | c.81+20722_81+20724d others(5): Show |
TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 38582346 | |||||
| chrX:38582346
|
TTTC | T | 1 | a0001c0001t0001g0185 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.81+20722_81+20724d others(5): Show |
TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 38582346 | |||||
| chrX:38582753
|
A | T | 3 | a0001c0001t0001g0110a0001c0001t0001g0174a0001c0001t0002g0109 | 3 | HG02602.hp1 HG03831.hp2 NA20805.hp1 |
intron_variant | MODIFIER | c.81+21126A>T | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38582753 | ||||||
| chrX:38582825
|
T | C | 14 | a0001c0001t0001g0082a0001c0001t0001g0083a0001c0001t0001g0185others(11): Show | 14 | HG01884.hp2 HG01891.hp2 HG02109.hp1 others(11): Show |
intron_variant | MODIFIER | c.81+21198T>C | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38582825 | ||||||
| chrX:38583396
|
G | A | 2 | a0001c0001t0001g0199a0001c0003t0001g0200 | 2 | HG02559.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.81+21769G>A | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38583396 | ||||||
| chrX:38583440
|
A | G | 1 | a0001c0001t0005g0078 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.81+21813A>G | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38583440 | ||||||
| chrX:38583462
|
A | G | 211 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(208): Show | 218 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(215): Show |
intron_variant | MODIFIER | c.81+21835A>G | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38583462 | ||||||
| chrX:38583531
|
T | C | 1 | a0001c0001t0001g0070 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.81+21904T>C | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38583531 | ||||||
| chrX:38583625
|
T | TG | 1 | a0002c0004t0001g0173 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.81+22000dupG | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 38583625 | |||||
| chrX:38583748
|
T | G | 2 | a0001c0001t0002g0208a0001c0003t0004g0207 | 2 | HG02109.hp2 HG02818.hp2 |
intron_variant | MODIFIER | c.81+22121T>G | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38583748 | ||||||
| chrX:38583871
|
T | A | 12 | a0001c0001t0001g0082a0001c0001t0001g0083a0001c0001t0001g0185others(9): Show | 12 | HG01884.hp2 HG01891.hp2 HG02109.hp1 others(9): Show |
intron_variant | MODIFIER | c.81+22244T>A | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38583871 | ||||||
| chrX:38583925
|
A | AT | 3 | a0001c0001t0001g0050a0001c0001t0002g0080a0001c0001t0003g0079 | 3 | HG02040.hp1 HG02630.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.81+22307dupT | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 38583925 | |||||
| chrX:38583925
|
AT | A | 1 | a0001c0001t0002g0127 | 1 | HG01517.hp2 | intron_variant | MODIFIER | c.81+22307delT | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 38583925 | |||||
| chrX:38583934
|
T | TTC | 1 | a0002c0004t0001g0173 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.81+22307_81+22308i others(4): Show |
TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38583934 | ||||||
| chrX:38583935
|
C | CT | 2 | a0001c0001t0001g0115a0001c0001t0001g0168 | 2 | NA18940.hp1 NA19004.hp1 |
intron_variant | MODIFIER | c.81+22316dupT | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 38583935 | |||||
| chrX:38583935
|
C | T | 1 | a0002c0004t0001g0173 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.81+22308C>T | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38583935 | ||||||
| chrX:38583939
|
TTTTTCTT others(3): Show |
T | 2 | a0001c0001t0002g0208a0001c0003t0004g0207 | 2 | HG02109.hp2 HG02818.hp2 |
intron_variant | MODIFIER | c.81+22317_81+22326d others(12): Show |
TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 38583939 | |||||
| chrX:38583942
|
T | C | 1 | a0001c0001t0001g0193 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.81+22315T>C | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38583942 | ||||||
| chrX:38583945
|
T | TTC | 1 | a0001c0001t0001g0193 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.81+22319_81+22320i others(4): Show |
TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 38583945 | |||||
| chrX:38583949
|
C | CT | 20 | a0001c0001t0001g0026a0001c0001t0001g0027a0001c0001t0001g0047others(17): Show | 20 | HG01175.hp2 HG01255.hp1 HG01891.hp2 others(17): Show |
intron_variant | MODIFIER | c.81+22344dupT | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 38583949 | |||||
| chrX:38583949
|
CT | C | 8 | a0001c0001t0001g0075a0001c0001t0001g0128a0001c0001t0001g0129others(5): Show | 8 | HG01167.hp1 HG01884.hp2 HG02109.hp1 others(5): Show |
intron_variant | MODIFIER | c.81+22344delT | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 38583949 | |||||
| chrX:38583949
|
CTTTTTTT others(2): Show |
C | 1 | a0001c0001t0001g0070 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.81+22336_81+22344d others(11): Show |
TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 38583949 | |||||
| chrX:38583950
|
T | C | 2 | a0001c0001t0002g0208a0001c0003t0004g0207 | 2 | HG02109.hp2 HG02818.hp2 |
intron_variant | MODIFIER | c.81+22323T>C | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38583950 | ||||||
| chrX:38583980
|
G | T | 7 | a0001c0001t0001g0087a0001c0001t0001g0089a0001c0001t0001g0090others(4): Show | 8 | HG01884.hp1 HG02559.hp2 HG02572.hp1 others(5): Show |
intron_variant | MODIFIER | c.81+22353G>T | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38583980 | ||||||
| chrX:38584162
|
C | T | 1 | a0001c0001t0002g0052 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.81+22535C>T | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38584162 | ||||||
| chrX:38584164
|
AGGAT | A | 1 | a0001c0001t0002g0052 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.81+22540_81+22543d others(6): Show |
TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 38584164 | |||||
| chrX:38584206
|
G | GC | 1 | a0002c0004t0001g0173 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.81+22581dupC | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 38584206 | |||||
| chrX:38584377
|
G | A | 215 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(212): Show | 222 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(219): Show |
intron_variant | MODIFIER | c.81+22750G>A | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38584377 | ||||||
| chrX:38584386
|
A | AT | 1 | a0001c0001t0001g0193 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.81+22761dupT | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 38584386 | |||||
| chrX:38584402
|
G | T | 1 | a0001c0001t0001g0185 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.81+22775G>T | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38584402 | ||||||
| chrX:38584441
|
C | A | 5 | a0001c0001t0001g0110a0001c0001t0001g0131a0001c0001t0001g0174others(2): Show | 5 | HG02602.hp1 HG03704.hp1 HG03831.hp2 others(2): Show |
intron_variant | MODIFIER | c.81+22814C>A | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38584441 | ||||||
| chrX:38584489
|
AT | A | 1 | a0001c0001t0001g0193 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.81+22865delT | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 38584489 | |||||
| chrX:38584513
|
CA | C | 1 | a0001c0001t0001g0193 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.81+22889delA | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 38584513 | |||||
| chrX:38584540
|
C | T | 2 | a0001c0001t0001g0199a0001c0003t0001g0200 | 2 | HG02559.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.81+22913C>T | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38584540 | ||||||
| chrX:38584626
|
A | G | 1 | a0001c0003t0001g0200 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.81+22999A>G | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38584626 | ||||||
| chrX:38584670
|
T | C | 1 | a0001c0001t0001g0176 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.81+23043T>C | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38584670 | ||||||
| chrX:38584866
|
A | G | 1 | a0001c0001t0002g0167 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.81+23239A>G | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38584866 | ||||||
| chrX:38585342
|
T | C | 6 | a0001c0001t0001g0059a0001c0001t0001g0060a0001c0001t0001g0061others(3): Show | 6 | HG02723.hp2 HG02809.hp1 HG02896.hp2 others(3): Show |
intron_variant | MODIFIER | c.81+23715T>C | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38585342 | ||||||
| chrX:38585410
|
G | A | 1 | a0001c0001t0002g0065 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.81+23783G>A | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38585410 | ||||||
| chrX:38585539
|
A | G | 1 | a0001c0001t0002g0172 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.81+23912A>G | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38585539 | ||||||
| chrX:38585613
|
T | C | 3 | a0001c0001t0001g0082a0001c0001t0001g0083a0001c0001t0002g0081 | 3 | HG01891.hp2 HG03098.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.81+23986T>C | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38585613 | ||||||
| chrX:38585657
|
A | G | 2 | a0001c0001t0001g0008a0001c0001t0001g0086 | 2 | NA18944.hp1 NA18955.hp1 |
intron_variant | MODIFIER | c.81+24030A>G | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38585657 | ||||||
| chrX:38585738
|
A | ATCC | 12 | a0001c0001t0001g0082a0001c0001t0001g0083a0001c0001t0001g0185others(9): Show | 12 | HG01884.hp2 HG01891.hp2 HG02109.hp1 others(9): Show |
intron_variant | MODIFIER | c.81+24113_81+24115d others(5): Show |
TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 38585738 | |||||
| chrX:38586192
|
G | A | 1 | a0001c0001t0001g0033 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.81+24565G>A | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38586192 | ||||||
| chrX:38586310
|
T | G | 12 | a0001c0001t0001g0082a0001c0001t0001g0083a0001c0001t0001g0185others(9): Show | 12 | HG01884.hp2 HG01891.hp2 HG02109.hp1 others(9): Show |
intron_variant | MODIFIER | c.81+24683T>G | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38586310 | ||||||
| chrX:38586310
|
TC | T | 7 | a0001c0001t0001g0008a0001c0001t0001g0034a0001c0001t0001g0035others(4): Show | 7 | HG00741.hp1 HG02027.hp1 NA18942.hp2 others(4): Show |
intron_variant | MODIFIER | c.81+24684delC | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38586310 | ||||||
| chrX:38586331
|
G | C | 1 | a0001c0001t0001g0170 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.81+24704G>C | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38586331 | ||||||
| chrX:38587168
|
G | A | 3 | a0001c0001t0001g0082a0001c0001t0001g0083a0001c0001t0002g0081 | 3 | HG01891.hp2 HG03098.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.81+25541G>A | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38587168 | ||||||
| chrX:38587301
|
T | C | 2 | a0001c0001t0001g0199a0001c0003t0001g0200 | 2 | HG02559.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.81+25674T>C | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38587301 | ||||||
| chrX:38587348
|
T | C | 1 | a0001c0001t0001g0053 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.81+25721T>C | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38587348 | ||||||
| chrX:38587368
|
A | G | 1 | a0001c0003t0001g0181 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.81+25741A>G | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38587368 | ||||||
| chrX:38587490
|
T | C | 3 | a0001c0001t0001g0082a0001c0001t0001g0083a0001c0001t0002g0081 | 3 | HG01891.hp2 HG03098.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.81+25863T>C | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38587490 | ||||||
| chrX:38587758
|
C | T | 1 | a0001c0001t0001g0180 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.81+26131C>T | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38587758 | ||||||
| chrX:38587806
|
C | T | 1 | a0001c0001t0002g0028 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.81+26179C>T | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38587806 | ||||||
| chrX:38587968
|
A | G | 2 | a0001c0001t0001g0129a0001c0001t0001g0164 | 2 | HG01167.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.81+26341A>G | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38587968 | ||||||
| chrX:38588002
|
G | A | 1 | a0001c0001t0001g0077 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.81+26375G>A | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38588002 | ||||||
| chrX:38588272
|
A | G | 1 | a0001c0001t0001g0083 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.81+26645A>G | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38588272 | ||||||
| chrX:38588335
|
T | G | 1 | a0001c0001t0002g0028 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.81+26708T>G | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38588335 | ||||||
| chrX:38588597
|
T | G | 12 | a0001c0001t0001g0082a0001c0001t0001g0083a0001c0001t0001g0185others(9): Show | 12 | HG01884.hp2 HG01891.hp2 HG02109.hp1 others(9): Show |
intron_variant | MODIFIER | c.81+26970T>G | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38588597 | ||||||
| chrX:38588613
|
G | A | 1 | a0001c0001t0001g0132 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.81+26986G>A | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38588613 | ||||||
| chrX:38588751
|
C | T | 1 | a0001c0001t0001g0070 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.81+27124C>T | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38588751 | ||||||
| chrX:38588891
|
C | T | 6 | a0001c0001t0001g0006a0001c0001t0001g0178a0001c0001t0001g0180others(3): Show | 7 | HG00099.hp2 HG00642.hp1 HG01069.hp1 others(4): Show |
intron_variant | MODIFIER | c.81+27264C>T | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38588891 | ||||||
| chrX:38589246
|
G | A | 3 | a0001c0001t0001g0185a0001c0001t0001g0202a0001c0003t0001g0201 | 3 | HG01884.hp2 HG04228.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.81+27619G>A | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38589246 | ||||||
| chrX:38589754
|
C | T | 14 | a0001c0001t0001g0082a0001c0001t0001g0083a0001c0001t0001g0185others(11): Show | 14 | HG01884.hp2 HG01891.hp2 HG02109.hp1 others(11): Show |
intron_variant | MODIFIER | c.81+28127C>T | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38589754 | ||||||
| chrX:38589769
|
A | G | 4 | a0001c0001t0001g0162a0001c0001t0001g0163a0001c0001t0001g0166others(1): Show | 4 | NA18960.hp1 NA18967.hp1 NA18989.hp1 others(1): Show |
intron_variant | MODIFIER | c.81+28142A>G | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38589769 | ||||||
| chrX:38589770
|
C | T | 1 | a0001c0001t0001g0185 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.81+28143C>T | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38589770 | ||||||
| chrX:38589861
|
C | T | 1 | a0001c0001t0001g0046 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.81+28234C>T | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38589861 | ||||||
| chrX:38589887
|
T | G | 1 | a0001c0001t0001g0162 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.81+28260T>G | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38589887 | ||||||
| chrX:38590110
|
T | A | 15 | a0001c0001t0001g0082a0001c0001t0001g0083a0001c0001t0001g0185others(12): Show | 15 | HG01884.hp2 HG01891.hp2 HG02109.hp1 others(12): Show |
intron_variant | MODIFIER | c.81+28483T>A | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38590110 | ||||||
| chrX:38590150
|
G | A | 1 | a0001c0003t0001g0215 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.81+28523G>A | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38590150 | ||||||
| chrX:38590816
|
C | A | 2 | a0001c0001t0001g0199a0001c0003t0001g0200 | 2 | HG02559.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.81+29189C>A | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38590816 | ||||||
| chrX:38591720
|
T | A | 1 | a0001c0001t0001g0034 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.81+30093T>A | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38591720 | ||||||
| chrX:38592148
|
G | A | 2 | a0001c0001t0001g0037a0001c0001t0001g0050 | 2 | HG02040.hp1 HG02083.hp1 |
intron_variant | MODIFIER | c.81+30521G>A | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38592148 | ||||||
| chrX:38592253
|
C | T | 1 | a0001c0002t0001g0074 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.81+30626C>T | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38592253 | ||||||
| chrX:38592294
|
G | A | 1 | a0001c0001t0002g0117 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.81+30667G>A | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38592294 | ||||||
| chrX:38592364
|
TG | T | 1 | a0001c0001t0001g0026 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.81+30740delG | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 38592364 | |||||
| chrX:38592442
|
A | AT | 1 | a0001c0001t0001g0026 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.81+30818dupT | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 38592442 | |||||
| chrX:38592481
|
T | C | 2 | a0001c0001t0001g0003a0001c0001t0001g0123 | 3 | HG01257.hp1 HG01981.hp1 HG01993.hp2 |
intron_variant | MODIFIER | c.81+30854T>C | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38592481 | ||||||
| chrX:38592520
|
C | CT | 1 | a0001c0001t0001g0026 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.81+30895dupT | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 38592520 | |||||
| chrX:38592644
|
C | G | 1 | a0001c0001t0002g0080 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.81+31017C>G | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38592644 | ||||||
| chrX:38592666
|
G | GC | 1 | a0001c0001t0001g0026 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.81+31041dupC | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 38592666 | |||||
| chrX:38592740
|
G | T | 1 | a0001c0001t0001g0026 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.81+31113G>T | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38592740 | ||||||
| chrX:38592764
|
T | TG | 1 | a0001c0001t0001g0026 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.81+31141dupG | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 38592764 | |||||
| chrX:38592774
|
C | G | 1 | a0001c0001t0001g0045 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.81+31147C>G | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38592774 | ||||||
| chrX:38592828
|
G | GA | 1 | a0001c0001t0001g0026 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.81+31207dupA | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 38592828 | |||||
| chrX:38592884
|
C | CA | 1 | a0001c0001t0001g0026 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.81+31258dupA | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 38592884 | |||||
| chrX:38593017
|
T | C | 1 | a0001c0001t0001g0077 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.81+31390T>C | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38593017 | ||||||
| chrX:38593087
|
A | AT | 1 | a0001c0001t0001g0026 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.81+31467dupT | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 38593087 | |||||
| chrX:38593172
|
G | GT | 1 | a0001c0001t0001g0026 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.81+31550dupT | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 38593172 | |||||
| chrX:38593509
|
T | G | 14 | a0001c0001t0001g0082a0001c0001t0001g0083a0001c0001t0001g0185others(11): Show | 14 | HG01884.hp2 HG01891.hp2 HG02109.hp1 others(11): Show |
intron_variant | MODIFIER | c.81+31882T>G | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38593509 | ||||||
| chrX:38593561
|
G | GT | 1 | a0001c0001t0001g0026 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.81+31935dupT | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 38593561 | |||||
| chrX:38593572
|
T | TG | 1 | a0001c0001t0001g0026 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.81+31948dupG | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 38593572 | |||||
| chrX:38593701
|
T | TA | 1 | a0001c0001t0001g0026 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.81+32074_81+32075i others(3): Show |
TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38593701 | ||||||
| chrX:38593710
|
CT | C | 1 | a0001c0001t0001g0026 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.81+32085delT | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 38593710 | |||||
| chrX:38593727
|
C | CT | 1 | a0001c0001t0001g0026 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.81+32103dupT | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 38593727 | |||||
| chrX:38593755
|
GC | G | 1 | a0001c0001t0001g0026 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.81+32131delC | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 38593755 | |||||
| chrX:38594171
|
G | GT | 1 | a0001c0001t0001g0026 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.81+32551dupT | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 38594171 | |||||
| chrX:38594224
|
G | GC | 1 | a0001c0001t0001g0026 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.81+32598dupC | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 38594224 | |||||
| chrX:38594237
|
G | GC | 1 | a0001c0001t0001g0026 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.81+32612dupC | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 38594237 | |||||
| chrX:38594278
|
CT | C | 1 | a0001c0001t0001g0026 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.81+32655delT | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 38594278 | |||||
| chrX:38594364
|
T | TC | 1 | a0001c0001t0001g0026 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.81+32741dupC | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 38594364 | |||||
| chrX:38594447
|
AG | A | 1 | a0001c0001t0001g0026 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.81+32823delG | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 38594447 | |||||
| chrX:38594485
|
CT | C | 1 | a0001c0001t0002g0020 | 1 | NA19055.hp1 | intron_variant | MODIFIER | c.81+32863delT | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 38594485 | |||||
| chrX:38594676
|
TA | T | 1 | a0001c0001t0002g0020 | 1 | NA19055.hp1 | intron_variant | MODIFIER | c.81+33054delA | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 38594676 | |||||
| chrX:38594798
|
T | TG | 1 | a0001c0001t0001g0026 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.81+33173dupG | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 38594798 | |||||
| chrX:38594866
|
C | T | 1 | a0001c0001t0001g0083 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.81+33239C>T | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38594866 | ||||||
| chrX:38594949
|
G | GA | 1 | a0001c0001t0001g0026 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.81+33323dupA | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 38594949 | |||||
| chrX:38595077
|
C | T | 4 | a0001c0001t0001g0035a0001c0001t0001g0036a0001c0001t0002g0028others(1): Show | 4 | HG00741.hp1 HG02976.hp2 NA18522.hp1 others(1): Show |
intron_variant | MODIFIER | c.81+33450C>T | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38595077 | ||||||
| chrX:38595098
|
AT | A | 1 | a0001c0001t0001g0115 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.81+33478delT | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 38595098 | |||||
| chrX:38595116
|
CT | C | 1 | a0001c0001t0001g0115 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.81+33492delT | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 38595116 | |||||
| chrX:38595215
|
A | G | 14 | a0001c0001t0001g0082a0001c0001t0001g0083a0001c0001t0001g0185others(11): Show | 14 | HG01884.hp2 HG01891.hp2 HG02109.hp1 others(11): Show |
intron_variant | MODIFIER | c.81+33588A>G | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38595215 | ||||||
| chrX:38595227
|
T | A | 1 | a0001c0001t0001g0026 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.81+33600T>A | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38595227 | ||||||
| chrX:38595247
|
G | GT | 1 | a0001c0001t0001g0026 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.81+33624dupT | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 38595247 | |||||
| chrX:38595259
|
G | A | 84 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(81): Show | 85 | HG00609.hp1 HG00621.hp1 HG00741.hp1 others(82): Show |
intron_variant | MODIFIER | c.81+33632G>A | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38595259 | ||||||
| chrX:38595273
|
G | A | 2 | a0001c0001t0001g0199a0001c0003t0001g0200 | 2 | HG02559.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.81+33646G>A | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38595273 | ||||||
| chrX:38595585
|
C | T | 12 | a0001c0001t0001g0082a0001c0001t0001g0083a0001c0001t0001g0185others(9): Show | 12 | HG01884.hp2 HG01891.hp2 HG02109.hp1 others(9): Show |
intron_variant | MODIFIER | c.81+33958C>T | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38595585 | ||||||
| chrX:38595691
|
T | TC | 1 | a0001c0001t0001g0115 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.81+34064_81+34065i others(3): Show |
TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38595691 | ||||||
| chrX:38595743
|
A | G | 1 | a0001c0001t0002g0124 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.81+34116A>G | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38595743 | ||||||
| chrX:38595756
|
C | CA | 1 | a0001c0001t0001g0026 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.81+34132dupA | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 38595756 | |||||
| chrX:38595894
|
G | GT | 1 | a0001c0001t0001g0026 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.81+34269dupT | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 38595894 | |||||
| chrX:38596105
|
TG | T | 1 | a0001c0001t0001g0115 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.81+34483delG | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 38596105 | |||||
| chrX:38596228
|
G | A | 12 | a0001c0001t0001g0082a0001c0001t0001g0083a0001c0001t0001g0185others(9): Show | 12 | HG01884.hp2 HG01891.hp2 HG02109.hp1 others(9): Show |
intron_variant | MODIFIER | c.81+34601G>A | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38596228 | ||||||
| chrX:38596281
|
T | A | 1 | a0001c0001t0001g0075 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.81+34654T>A | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38596281 | ||||||
| chrX:38596548
|
T | TC | 1 | a0001c0001t0001g0026 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.81+34922dupC | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 38596548 | |||||
| chrX:38596605
|
C | T | 1 | a0001c0001t0002g0069 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.81+34978C>T | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38596605 | ||||||
| chrX:38596711
|
C | T | 1 | a0001c0001t0001g0185 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.81+35084C>T | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38596711 | ||||||
| chrX:38597134
|
A | AC | 1 | a0001c0001t0001g0026 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.81+35508dupC | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 38597134 | |||||
| chrX:38597286
|
C | T | 1 | a0001c0003t0001g0181 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.81+35659C>T | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38597286 | ||||||
| chrX:38597295
|
G | GC | 1 | a0001c0001t0001g0026 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.81+35669dupC | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 38597295 | |||||
| chrX:38597302
|
T | A | 1 | a0001c0001t0001g0185 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.81+35675T>A | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38597302 | ||||||
| chrX:38597316
|
A | ATT | 2 | a0001c0001t0001g0199a0001c0003t0001g0200 | 2 | HG02559.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.81+35697_81+35698d others(4): Show |
TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 38597316 | |||||
| chrX:38597316
|
AT | A | 1 | a0001c0001t0002g0022 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.81+35698delT | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 38597316 | |||||
| chrX:38597345
|
G | GT | 1 | a0001c0001t0001g0026 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.81+35723dupT | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 38597345 | |||||
| chrX:38597364
|
CT | C | 1 | a0001c0001t0001g0026 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.81+35740delT | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 38597364 | |||||
| chrX:38597525
|
A | G | 1 | a0001c0001t0001g0082 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.81+35898A>G | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38597525 | ||||||
| chrX:38597533
|
A | C | 1 | a0001c0001t0005g0078 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.81+35906A>C | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38597533 | ||||||
| chrX:38597708
|
T | G | 1 | a0001c0001t0001g0099 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.81+36081T>G | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38597708 | ||||||
| chrX:38597754
|
T | TA | 1 | a0001c0001t0001g0026 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.81+36131dupA | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 38597754 | |||||
| chrX:38597864
|
AT | A | 1 | a0001c0001t0001g0115 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.81+36240delT | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 38597864 | |||||
| chrX:38597869
|
A | T | 1 | a0001c0001t0001g0115 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.81+36242A>T | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38597869 | ||||||
| chrX:38597871
|
A | T | 1 | a0001c0001t0001g0115 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.81+36244A>T | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38597871 | ||||||
| chrX:38597872
|
T | A | 1 | a0001c0001t0001g0115 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.81+36245T>A | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38597872 | ||||||
| chrX:38597873
|
A | C | 1 | a0001c0001t0001g0115 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.81+36246A>C | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38597873 | ||||||
| chrX:38597877
|
A | G | 1 | a0001c0001t0001g0115 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.81+36250A>G | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38597877 | ||||||
| chrX:38597878
|
T | TA | 1 | a0001c0001t0001g0026 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.81+36253dupA | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 38597878 | |||||
| chrX:38597879
|
A | G | 1 | a0001c0001t0001g0115 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.81+36252A>G | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38597879 | ||||||
| chrX:38597880
|
AC | A | 1 | a0001c0001t0001g0115 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.81+36254delC | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38597880 | ||||||
| chrX:38597884
|
G | T | 1 | a0001c0001t0001g0115 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.81+36257G>T | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38597884 | ||||||
| chrX:38597885
|
TAA | T | 1 | a0001c0001t0001g0115 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.81+36259_81+36260d others(4): Show |
TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38597885 | ||||||
| chrX:38597929
|
T | TG | 1 | a0001c0001t0001g0026 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.81+36304dupG | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 38597929 | |||||
| chrX:38597935
|
C | T | 2 | a0001c0001t0001g0044a0001c0001t0001g0075 | 2 | HG01934.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.81+36308C>T | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38597935 | ||||||
| chrX:38598276
|
C | T | 1 | a0001c0001t0002g0102 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.81+36649C>T | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38598276 | ||||||
| chrX:38598342
|
AG | A | 1 | a0001c0001t0001g0026 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.81+36716delG | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38598342 | ||||||
| chrX:38598540
|
T | TC | 1 | a0001c0001t0001g0115 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.81+36919dupC | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 38598540 | |||||
| chrX:38598714
|
C | CT | 1 | a0001c0001t0002g0161 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.81+37090dupT | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 38598714 | |||||
| chrX:38598766
|
G | GA | 1 | a0001c0001t0002g0161 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.81+37143dupA | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 38598766 | |||||
| chrX:38598799
|
A | T | 1 | a0001c0001t0002g0161 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.81+37172A>T | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38598799 | ||||||
| chrX:38598814
|
G | GA | 1 | a0001c0001t0002g0161 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.81+37193dupA | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 38598814 | |||||
| chrX:38598887
|
G | GT | 1 | a0001c0001t0002g0161 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.81+37264dupT | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 38598887 | |||||
| chrX:38599065
|
G | A | 2 | a0001c0001t0003g0057a0001c0001t0003g0058 | 2 | HG02976.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.81+37438G>A | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38599065 | ||||||
| chrX:38599155
|
G | T | 2 | a0001c0001t0001g0043a0001c0001t0001g0048 | 2 | NA18961.hp1 NA18982.hp1 |
intron_variant | MODIFIER | c.81+37528G>T | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38599155 | ||||||
| chrX:38599375
|
TA | T | 1 | a0001c0001t0001g0113 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.81+37757delA | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 38599375 | |||||
| chrX:38599449
|
A | AT | 1 | a0001c0001t0002g0161 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.81+37823dupT | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 38599449 | |||||
| chrX:38600127
|
T | G | 1 | a0001c0001t0002g0191 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.81+38500T>G | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38600127 | ||||||
| chrX:38600245
|
C | T | 1 | a0001c0001t0001g0046 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.81+38618C>T | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38600245 | ||||||
| chrX:38600380
|
A | AC | 1 | a0001c0001t0002g0161 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.81+38758dupC | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 38600380 | |||||
| chrX:38600800
|
A | G | 1 | a0001c0001t0001g0202 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.81+39173A>G | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38600800 | ||||||
| chrX:38600898
|
T | C | 9 | a0001c0001t0001g0185a0001c0001t0001g0202a0001c0001t0001g0203others(6): Show | 9 | HG01884.hp2 HG02109.hp1 HG02109.hp2 others(6): Show |
intron_variant | MODIFIER | c.81+39271T>C | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38600898 | ||||||
| chrX:38601263
|
A | G | 1 | a0001c0001t0002g0028 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.81+39636A>G | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38601263 | ||||||
| chrX:38601419
|
A | G | 27 | a0001c0001t0001g0054a0001c0001t0001g0056a0001c0001t0001g0059others(24): Show | 27 | HG01255.hp1 HG02055.hp1 HG02132.hp1 others(24): Show |
intron_variant | MODIFIER | c.81+39792A>G | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38601419 | ||||||
| chrX:38601692
|
T | C | 4 | a0001c0001t0001g0119a0001c0001t0001g0120a0001c0001t0001g0121others(1): Show | 4 | HG01109.hp1 HG01256.hp1 HG01358.hp1 others(1): Show |
intron_variant | MODIFIER | c.81+40065T>C | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38601692 | ||||||
| chrX:38601965
|
A | G | 1 | a0001c0001t0001g0176 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.81+40338A>G | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38601965 | ||||||
| chrX:38601989
|
A | G | 3 | a0001c0001t0001g0026a0001c0001t0001g0043a0001c0001t0001g0048 | 3 | NA18961.hp1 NA18982.hp1 NA19078.hp2 |
intron_variant | MODIFIER | c.81+40362A>G | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38601989 | ||||||
| chrX:38602274
|
A | G | 10 | a0001c0001t0001g0006a0001c0001t0001g0170a0001c0001t0001g0178others(7): Show | 11 | HG00099.hp2 HG00642.hp1 HG01069.hp1 others(8): Show |
intron_variant | MODIFIER | c.81+40647A>G | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38602274 | ||||||
| chrX:38602615
|
A | G | 3 | a0001c0001t0001g0026a0001c0001t0001g0043a0001c0001t0001g0048 | 3 | NA18961.hp1 NA18982.hp1 NA19078.hp2 |
intron_variant | MODIFIER | c.81+40988A>G | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38602615 | ||||||
| chrX:38602870
|
G | C | 1 | a0001c0003t0001g0201 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.81+41243G>C | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38602870 | ||||||
| chrX:38602978
|
A | C | 1 | a0001c0002t0001g0088 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.81+41351A>C | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38602978 | ||||||
| chrX:38603120
|
T | C | 7 | a0001c0001t0002g0065a0001c0001t0002g0067a0001c0001t0002g0069others(4): Show | 7 | HG02257.hp1 HG02896.hp1 HG02976.hp1 others(4): Show |
intron_variant | MODIFIER | c.81+41493T>C | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38603120 | ||||||
| chrX:38603213
|
A | G | 80 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(77): Show | 81 | HG00609.hp1 HG00621.hp1 HG00741.hp1 others(78): Show |
intron_variant | MODIFIER | c.81+41586A>G | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38603213 | ||||||
| chrX:38603506
|
C | T | 1 | a0001c0001t0002g0209 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.81+41879C>T | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38603506 | ||||||
| chrX:38603847
|
TTTTA | T | 12 | a0001c0001t0001g0082a0001c0001t0001g0083a0001c0001t0001g0185others(9): Show | 12 | HG01884.hp2 HG01891.hp2 HG02109.hp1 others(9): Show |
intron_variant | MODIFIER | c.81+42240_81+42243d others(6): Show |
TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 38603847 | |||||
| chrX:38604016
|
T | TC | 2 | a0001c0001t0001g0174a0002c0004t0001g0173 | 2 | HG03831.hp2 NA18985.hp1 |
intron_variant | MODIFIER | c.81+42395dupC | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 38604016 | |||||
| chrX:38604023
|
T | TC | 2 | a0001c0001t0001g0072a0001c0001t0001g0169 | 2 | HG02055.hp1 NA18991.hp2 |
intron_variant | MODIFIER | c.81+42402dupC | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 38604023 | |||||
| chrX:38604024
|
C | CT | 1 | a0001c0001t0001g0026 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.81+42397_81+42398i others(3): Show |
TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38604024 | ||||||
| chrX:38604125
|
T | C | 1 | a0001c0001t0001g0077 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.81+42498T>C | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38604125 | ||||||
| chrX:38604207
|
A | AT | 1 | a0001c0001t0001g0077 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.81+42586dupT | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 38604207 | |||||
| chrX:38604482
|
CCCA | C | 1 | a0001c0001t0001g0185 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.81+42859_81+42861d others(5): Show |
TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 38604482 | |||||
| chrX:38604500
|
G | T | 9 | a0001c0001t0001g0185a0001c0001t0001g0202a0001c0001t0001g0203others(6): Show | 9 | HG01884.hp2 HG02109.hp1 HG02109.hp2 others(6): Show |
intron_variant | MODIFIER | c.81+42873G>T | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38604500 | ||||||
| chrX:38604558
|
C | G | 2 | a0001c0001t0001g0199a0001c0003t0001g0200 | 2 | HG02559.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.81+42931C>G | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38604558 | ||||||
| chrX:38604760
|
C | G | 1 | a0001c0001t0001g0160 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.81+43133C>G | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38604760 | ||||||
| chrX:38604940
|
C | T | 1 | a0001c0001t0003g0079 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.81+43313C>T | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38604940 | ||||||
| chrX:38604941
|
G | A | 3 | a0001c0001t0001g0082a0001c0001t0001g0083a0001c0001t0002g0081 | 3 | HG01891.hp2 HG03098.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.81+43314G>A | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38604941 | ||||||
| chrX:38604992
|
A | G | 3 | a0001c0001t0001g0082a0001c0001t0001g0083a0001c0001t0002g0081 | 3 | HG01891.hp2 HG03098.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.81+43365A>G | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38604992 | ||||||
| chrX:38605040
|
G | A | 1 | a0001c0001t0001g0210 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.81+43413G>A | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38605040 | ||||||
| chrX:38605058
|
G | A | 12 | a0001c0001t0001g0082a0001c0001t0001g0083a0001c0001t0001g0185others(9): Show | 12 | HG01884.hp2 HG01891.hp2 HG02109.hp1 others(9): Show |
intron_variant | MODIFIER | c.81+43431G>A | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38605058 | ||||||
| chrX:38605221
|
A | T | 80 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(77): Show | 81 | HG00609.hp1 HG00621.hp1 HG00741.hp1 others(78): Show |
intron_variant | MODIFIER | c.81+43594A>T | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38605221 | ||||||
| chrX:38605261
|
C | T | 7 | a0001c0001t0001g0059a0001c0001t0001g0060a0001c0001t0001g0061others(4): Show | 7 | HG02723.hp2 HG02809.hp1 HG02896.hp2 others(4): Show |
intron_variant | MODIFIER | c.81+43634C>T | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38605261 | ||||||
| chrX:38605262
|
G | A | 1 | a0001c0001t0001g0093 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.81+43635G>A | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38605262 | ||||||
| chrX:38605465
|
C | T | 1 | a0001c0001t0002g0028 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.81+43838C>T | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38605465 | ||||||
| chrX:38605592
|
C | T | 1 | a0001c0002t0001g0092 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.81+43965C>T | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38605592 | ||||||
| chrX:38605597
|
C | T | 1 | a0001c0001t0002g0028 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.81+43970C>T | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38605597 | ||||||
| chrX:38605784
|
A | G | 3 | a0001c0001t0001g0082a0001c0001t0001g0083a0001c0001t0002g0081 | 3 | HG01891.hp2 HG03098.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.81+44157A>G | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38605784 | ||||||
| chrX:38605881
|
C | T | 1 | a0001c0001t0001g0116 | 1 | HG01071.hp2 | intron_variant | MODIFIER | c.81+44254C>T | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38605881 | ||||||
| chrX:38606077
|
A | C | 1 | a0001c0001t0001g0159 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.81+44450A>C | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38606077 | ||||||
| chrX:38606215
|
GA | G | 1 | a0001c0001t0005g0078 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.81+44595delA | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 38606215 | |||||
| chrX:38606285
|
A | G | 12 | a0001c0001t0001g0082a0001c0001t0001g0083a0001c0001t0001g0185others(9): Show | 12 | HG01884.hp2 HG01891.hp2 HG02109.hp1 others(9): Show |
intron_variant | MODIFIER | c.81+44658A>G | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38606285 | ||||||
| chrX:38606322
|
A | G | 4 | a0001c0001t0001g0203a0001c0001t0001g0204a0001c0001t0001g0205others(1): Show | 4 | HG02109.hp1 HG02145.hp1 HG02630.hp1 others(1): Show |
intron_variant | MODIFIER | c.81+44695A>G | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38606322 | ||||||
| chrX:38606323
|
A | AAAATATT | 1 | a0001c0001t0001g0033 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.81+44701_81+44707d others(9): Show |
TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 38606323 | |||||
| chrX:38606368
|
A | C | 1 | a0001c0001t0002g0017 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.81+44741A>C | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38606368 | ||||||
| chrX:38606371
|
G | A | 1 | a0001c0001t0001g0113 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.81+44744G>A | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38606371 | ||||||
| chrX:38606382
|
T | A | 62 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0049others(59): Show | 64 | HG00438.hp1 HG00673.hp1 HG00738.hp1 others(61): Show |
intron_variant | MODIFIER | c.81+44755T>A | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38606382 | ||||||
| chrX:38606410
|
T | TG | 1 | a0001c0001t0002g0133 | 1 | NA19078.hp1 | intron_variant | MODIFIER | c.81+44789dupG | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 38606410 | |||||
| chrX:38606470
|
G | T | 1 | a0001c0001t0001g0077 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.81+44843G>T | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38606470 | ||||||
| chrX:38607049
|
G | A | 12 | a0001c0001t0001g0082a0001c0001t0001g0083a0001c0001t0001g0185others(9): Show | 12 | HG01884.hp2 HG01891.hp2 HG02109.hp1 others(9): Show |
intron_variant | MODIFIER | c.81+45422G>A | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38607049 | ||||||
| chrX:38607399
|
G | A | 1 | a0001c0001t0001g0051 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.81+45772G>A | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38607399 | ||||||
| chrX:38607521
|
C | T | 2 | a0001c0001t0002g0028a0001c0002t0001g0092 | 2 | HG02976.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.81+45894C>T | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38607521 | ||||||
| chrX:38607788
|
T | C | 16 | a0001c0001t0001g0082a0001c0001t0001g0083a0001c0001t0001g0185others(13): Show | 16 | HG01884.hp2 HG01891.hp2 HG02109.hp1 others(13): Show |
intron_variant | MODIFIER | c.81+46161T>C | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38607788 | ||||||
| chrX:38607862
|
G | GA | 1 | a0001c0001t0001g0115 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.81+46251dupA | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 38607862 | |||||
| chrX:38607862
|
GA | G | 13 | a0001c0001t0001g0082a0001c0001t0001g0083a0001c0001t0001g0185others(10): Show | 13 | HG01884.hp2 HG01891.hp2 HG02109.hp1 others(10): Show |
intron_variant | MODIFIER | c.81+46251delA | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 38607862 | |||||
| chrX:38608085
|
A | G | 1 | a0001c0002t0001g0092 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.81+46458A>G | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38608085 | ||||||
| chrX:38608091
|
G | A | 2 | a0001c0001t0001g0054a0001c0001t0001g0176 | 2 | HG02132.hp1 NA18991.hp1 |
intron_variant | MODIFIER | c.81+46464G>A | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38608091 | ||||||
| chrX:38608205
|
TA | T | 12 | a0001c0001t0001g0082a0001c0001t0001g0083a0001c0001t0001g0185others(9): Show | 12 | HG01884.hp2 HG01891.hp2 HG02109.hp1 others(9): Show |
intron_variant | MODIFIER | c.81+46586delA | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 38608205 | |||||
| chrX:38608246
|
C | T | 1 | a0001c0003t0001g0215 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.81+46619C>T | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38608246 | ||||||
| chrX:38608299
|
A | T | 1 | a0001c0001t0001g0044 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.81+46672A>T | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38608299 | ||||||
| chrX:38608431
|
G | A | 1 | a0001c0001t0001g0103 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.81+46804G>A | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38608431 | ||||||
| chrX:38609042
|
C | CCT | 14 | a0001c0001t0001g0082a0001c0001t0001g0083a0001c0001t0001g0185others(11): Show | 14 | HG01884.hp2 HG01891.hp2 HG02109.hp1 others(11): Show |
intron_variant | MODIFIER | c.81+47415_81+47416i others(4): Show |
TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38609042 | ||||||
| chrX:38609196
|
G | A | 1 | a0001c0001t0002g0102 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.81+47569G>A | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38609196 | ||||||
| chrX:38609331
|
A | T | 1 | a0001c0001t0002g0124 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.81+47704A>T | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38609331 | ||||||
| chrX:38609424
|
A | C | 1 | a0001c0003t0004g0207 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.81+47797A>C | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38609424 | ||||||
| chrX:38609770
|
T | TA | 2 | a0001c0001t0001g0199a0001c0003t0001g0200 | 2 | HG02559.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.81+48149dupA | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 38609770 | |||||
| chrX:38609839
|
G | T | 4 | a0001c0001t0001g0203a0001c0001t0001g0204a0001c0001t0001g0205others(1): Show | 4 | HG02109.hp1 HG02145.hp1 HG02630.hp1 others(1): Show |
intron_variant | MODIFIER | c.81+48212G>T | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38609839 | ||||||
| chrX:38610056
|
C | T | 1 | a0001c0002t0001g0092 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.81+48429C>T | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38610056 | ||||||
| chrX:38610130
|
A | G | 108 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(105): Show | 110 | HG00609.hp1 HG00621.hp1 HG00741.hp1 others(107): Show |
intron_variant | MODIFIER | c.81+48503A>G | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38610130 | ||||||
| chrX:38610219
|
A | G | 14 | a0001c0001t0001g0082a0001c0001t0001g0083a0001c0001t0001g0185others(11): Show | 14 | HG01884.hp2 HG01891.hp2 HG02109.hp1 others(11): Show |
intron_variant | MODIFIER | c.81+48592A>G | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38610219 | ||||||
| chrX:38610285
|
CA | C | 1 | a0001c0001t0001g0045 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.81+48659delA | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38610285 | ||||||
| chrX:38610314
|
C | G | 16 | a0001c0001t0001g0003a0001c0001t0001g0085a0001c0001t0001g0108others(13): Show | 17 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(14): Show |
intron_variant | MODIFIER | c.81+48687C>G | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38610314 | ||||||
| chrX:38610491
|
C | T | 52 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(49): Show | 53 | HG00609.hp1 HG00621.hp1 HG00741.hp1 others(50): Show |
intron_variant | MODIFIER | c.81+48864C>T | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38610491 | ||||||
| chrX:38610876
|
A | G | 1 | a0001c0001t0001g0190 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.81+49249A>G | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38610876 | ||||||
| chrX:38611014
|
G | A | 2 | a0001c0001t0002g0208a0001c0003t0004g0207 | 2 | HG02109.hp2 HG02818.hp2 |
intron_variant | MODIFIER | c.81+49387G>A | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38611014 | ||||||
| chrX:38611506
|
G | A | 1 | a0001c0002t0001g0214 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.81+49879G>A | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38611506 | ||||||
| chrX:38611708
|
T | C | 1 | a0001c0001t0001g0093 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.81+50081T>C | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38611708 | ||||||
| chrX:38612053
|
AT | A | 2 | a0001c0002t0001g0212a0001c0002t0001g0213 | 2 | HG03195.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.81+50428delT | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 38612053 | |||||
| chrX:38612078
|
C | T | 1 | a0001c0001t0001g0077 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.81+50451C>T | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38612078 | ||||||
| chrX:38612437
|
A | G | 9 | a0001c0001t0001g0185a0001c0001t0001g0202a0001c0001t0001g0203others(6): Show | 9 | HG01884.hp2 HG02109.hp1 HG02109.hp2 others(6): Show |
intron_variant | MODIFIER | c.81+50810A>G | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38612437 | ||||||
| chrX:38612548
|
C | T | 1 | a0001c0001t0001g0054 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.81+50921C>T | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38612548 | ||||||
| chrX:38612667
|
G | T | 1 | a0001c0001t0002g0020 | 1 | NA19055.hp1 | intron_variant | MODIFIER | c.81+51040G>T | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38612667 | ||||||
| chrX:38612682
|
C | T | 2 | a0001c0001t0002g0080a0001c0001t0003g0079 | 2 | HG02630.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.81+51055C>T | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38612682 | ||||||
| chrX:38612946
|
C | T | 1 | a0001c0001t0001g0071 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.81+51319C>T | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38612946 | ||||||
| chrX:38613031
|
C | G | 2 | a0001c0001t0001g0199a0001c0003t0001g0200 | 2 | HG02559.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.81+51404C>G | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38613031 | ||||||
| chrX:38613377
|
G | C | 4 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0011others(1): Show | 4 | HG01074.hp1 HG01169.hp2 HG01928.hp1 others(1): Show |
intron_variant | MODIFIER | c.81+51750G>C | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38613377 | ||||||
| chrX:38613564
|
T | C | 1 | a0001c0002t0001g0088 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.81+51937T>C | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38613564 | ||||||
| chrX:38613741
|
C | G | 3 | a0001c0001t0001g0023a0001c0001t0001g0185a0001c0003t0001g0066 | 3 | HG02965.hp1 HG03540.hp2 HG04228.hp1 |
intron_variant | MODIFIER | c.81+52114C>G | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38613741 | ||||||
| chrX:38613948
|
A | T | 2 | a0001c0001t0002g0080a0001c0001t0003g0079 | 2 | HG02630.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.82-52173A>T | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38613948 | ||||||
| chrX:38613972
|
G | GT | 2 | a0001c0001t0001g0044a0001c0001t0001g0103 | 2 | HG01934.hp1 NA19000.hp1 |
intron_variant | MODIFIER | c.82-52137dupT | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 38613972 | |||||
| chrX:38613972
|
GT | G | 3 | a0001c0001t0001g0187a0001c0001t0001g0199a0001c0001t0002g0208 | 3 | HG01884.hp1 HG02559.hp1 HG02818.hp2 |
intron_variant | MODIFIER | c.82-52137delT | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 38613972 | |||||
| chrX:38613981
|
T | C | 28 | a0001c0001t0001g0054a0001c0001t0001g0056a0001c0001t0001g0059others(25): Show | 29 | HG01255.hp1 HG01884.hp2 HG02055.hp1 others(26): Show |
intron_variant | MODIFIER | c.82-52140T>C | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38613981 | ||||||
| chrX:38613985
|
C | CT | 1 | a0001c0001t0002g0109 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.82-52125dupT | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 38613985 | |||||
| chrX:38614236
|
T | G | 1 | a0001c0001t0002g0191 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.82-51885T>G | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38614236 | ||||||
| chrX:38614331
|
A | G | 175 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(172): Show | 180 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(177): Show |
intron_variant | MODIFIER | c.82-51790A>G | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38614331 | ||||||
| chrX:38614457
|
C | G | 1 | a0001c0001t0001g0107 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.82-51664C>G | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38614457 | ||||||
| chrX:38614583
|
A | G | 1 | a0001c0001t0001g0055 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.82-51538A>G | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38614583 | ||||||
| chrX:38614803
|
T | C | 1 | a0001c0002t0001g0074 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.82-51318T>C | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38614803 | ||||||
| chrX:38614830
|
A | G | 89 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(86): Show | 92 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(89): Show |
intron_variant | MODIFIER | c.82-51291A>G | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38614830 | ||||||
| chrX:38614921
|
T | A | 169 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(166): Show | 174 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(171): Show |
intron_variant | MODIFIER | c.82-51200T>A | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38614921 | ||||||
| chrX:38614992
|
C | CT | 8 | a0001c0001t0001g0006a0001c0001t0001g0023a0001c0001t0001g0087others(5): Show | 10 | HG01257.hp2 HG01258.hp1 HG02559.hp2 others(7): Show |
intron_variant | MODIFIER | c.82-51118dupT | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 38614992 | |||||
| chrX:38614992
|
CT | C | 97 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(94): Show | 100 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(97): Show |
intron_variant | MODIFIER | c.82-51118delT | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 38614992 | |||||
| chrX:38615034
|
C | T | 3 | a0001c0001t0001g0203a0001c0001t0001g0205a0001c0001t0001g0206 | 3 | HG02145.hp1 HG02630.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.82-51087C>T | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38615034 | ||||||
| chrX:38615554
|
GT | G | 85 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(82): Show | 88 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(85): Show |
intron_variant | MODIFIER | c.82-50561delT | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 38615554 | |||||
| chrX:38615717
|
T | C | 1 | a0001c0001t0001g0075 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.82-50404T>C | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38615717 | ||||||
| chrX:38615756
|
C | T | 84 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(81): Show | 87 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(84): Show |
intron_variant | MODIFIER | c.82-50365C>T | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38615756 | ||||||
| chrX:38615982
|
A | G | 84 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(81): Show | 87 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(84): Show |
intron_variant | MODIFIER | c.82-50139A>G | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38615982 | ||||||
| chrX:38616132
|
A | G | 4 | a0001c0001t0001g0108a0001c0001t0002g0028a0001c0001t0002g0191others(1): Show | 4 | HG01243.hp1 HG02922.hp1 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.82-49989A>G | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38616132 | ||||||
| chrX:38616376
|
A | G | 1 | a0001c0001t0002g0172 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.82-49745A>G | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38616376 | ||||||
| chrX:38616389
|
T | C | 1 | a0001c0001t0001g0038 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.82-49732T>C | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38616389 | ||||||
| chrX:38616476
|
A | G | 49 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(46): Show | 51 | HG00609.hp1 HG00621.hp1 HG00741.hp1 others(48): Show |
intron_variant | MODIFIER | c.82-49645A>G | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38616476 | ||||||
| chrX:38616582
|
C | A | 1 | a0001c0001t0001g0089 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.82-49539C>A | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38616582 | ||||||
| chrX:38616824
|
A | G | 2 | a0001c0002t0001g0212a0001c0002t0001g0213 | 2 | HG03195.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.82-49297A>G | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38616824 | ||||||
| chrX:38617088
|
C | G | 1 | a0001c0002t0001g0074 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.82-49033C>G | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38617088 | ||||||
| chrX:38617117
|
A | G | 9 | a0001c0001t0002g0022a0001c0001t0002g0065a0001c0001t0002g0067others(6): Show | 9 | HG02109.hp2 HG02257.hp1 HG02630.hp2 others(6): Show |
intron_variant | MODIFIER | c.82-49004A>G | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38617117 | ||||||
| chrX:38617605
|
G | A | 84 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(81): Show | 87 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(84): Show |
intron_variant | MODIFIER | c.82-48516G>A | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38617605 | ||||||
| chrX:38617731
|
C | T | 84 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(81): Show | 87 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(84): Show |
intron_variant | MODIFIER | c.82-48390C>T | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38617731 | ||||||
| chrX:38617747
|
CCTT | C | 1 | a0001c0001t0001g0075 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.82-48371_82-48369d others(5): Show |
TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 38617747 | |||||
| chrX:38617940
|
G | A | 1 | a0001c0001t0002g0081 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.82-48181G>A | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38617940 | ||||||
| chrX:38618047
|
C | T | 9 | a0001c0001t0002g0022a0001c0001t0002g0065a0001c0001t0002g0067others(6): Show | 9 | HG02109.hp2 HG02257.hp1 HG02630.hp2 others(6): Show |
intron_variant | MODIFIER | c.82-48074C>T | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38618047 | ||||||
| chrX:38618069
|
G | A | 1 | a0001c0001t0001g0006 | 2 | HG01257.hp2 HG01258.hp1 |
intron_variant | MODIFIER | c.82-48052G>A | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38618069 | ||||||
| chrX:38618460
|
G | A | 1 | a0001c0001t0001g0072 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.82-47661G>A | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38618460 | ||||||
| chrX:38618752
|
G | A | 1 | a0001c0001t0001g0168 | 1 | NA19004.hp1 | intron_variant | MODIFIER | c.82-47369G>A | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38618752 | ||||||
| chrX:38618779
|
T | C | 1 | a0001c0001t0002g0021 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.82-47342T>C | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38618779 | ||||||
| chrX:38618936
|
G | A | 1 | a0001c0001t0001g0180 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.82-47185G>A | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38618936 | ||||||
| chrX:38618960
|
T | C | 4 | a0001c0001t0001g0004a0001c0001t0001g0118a0001c0001t0001g0140others(1): Show | 5 | HG00438.hp1 HG01175.hp1 HG01943.hp1 others(2): Show |
intron_variant | MODIFIER | c.82-47161T>C | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38618960 | ||||||
| chrX:38618990
|
A | G | 1 | a0001c0001t0001g0044 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.82-47131A>G | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38618990 | ||||||
| chrX:38619048
|
C | T | 97 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(94): Show | 100 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(97): Show |
intron_variant | MODIFIER | c.82-47073C>T | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38619048 | ||||||
| chrX:38619049
|
A | G | 176 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(173): Show | 181 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(178): Show |
intron_variant | MODIFIER | c.82-47072A>G | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38619049 | ||||||
| chrX:38619162
|
C | T | 1 | a0001c0001t0002g0149 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.82-46959C>T | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38619162 | ||||||
| chrX:38619208
|
C | T | 3 | a0001c0001t0001g0062a0001c0001t0001g0063a0001c0001t0001g0064 | 3 | HG02809.hp1 HG02896.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.82-46913C>T | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38619208 | ||||||
| chrX:38619246
|
T | C | 9 | a0001c0001t0002g0022a0001c0001t0002g0065a0001c0001t0002g0067others(6): Show | 9 | HG02109.hp2 HG02257.hp1 HG02630.hp2 others(6): Show |
intron_variant | MODIFIER | c.82-46875T>C | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38619246 | ||||||
| chrX:38619285
|
G | A | 1 | a0001c0001t0001g0194 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.82-46836G>A | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38619285 | ||||||
| chrX:38619368
|
A | G | 1 | a0001c0001t0001g0045 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.82-46753A>G | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38619368 | ||||||
| chrX:38619753
|
T | G | 2 | a0001c0001t0001g0083a0001c0001t0002g0081 | 2 | HG01891.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.82-46368T>G | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38619753 | ||||||
| chrX:38619953
|
C | T | 9 | a0001c0001t0002g0022a0001c0001t0002g0065a0001c0001t0002g0067others(6): Show | 9 | HG02109.hp2 HG02257.hp1 HG02630.hp2 others(6): Show |
intron_variant | MODIFIER | c.82-46168C>T | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38619953 | ||||||
| chrX:38620283
|
T | C | 6 | a0001c0001t0001g0077a0001c0001t0001g0084a0001c0001t0001g0199others(3): Show | 6 | HG02559.hp1 HG02615.hp1 HG02647.hp1 others(3): Show |
intron_variant | MODIFIER | c.82-45838T>C | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38620283 | ||||||
| chrX:38620332
|
C | T | 1 | a0001c0001t0001g0158 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.82-45789C>T | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38620332 | ||||||
| chrX:38620360
|
A | G | 1 | a0001c0001t0001g0202 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.82-45761A>G | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38620360 | ||||||
| chrX:38620615
|
C | T | 3 | a0001c0001t0001g0024a0001c0001t0001g0153a0001c0001t0001g0154 | 3 | HG00099.hp1 HG02735.hp1 HG03688.hp1 |
intron_variant | MODIFIER | c.82-45506C>T | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38620615 | ||||||
| chrX:38620640
|
T | G | 1 | a0001c0002t0001g0214 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.82-45481T>G | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38620640 | ||||||
| chrX:38620827
|
G | T | 84 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(81): Show | 87 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(84): Show |
intron_variant | MODIFIER | c.82-45294G>T | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38620827 | ||||||
| chrX:38620871
|
C | A | 1 | a0001c0001t0001g0075 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.82-45250C>A | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38620871 | ||||||
| chrX:38621144
|
G | A | 1 | a0001c0001t0001g0204 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.82-44977G>A | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38621144 | ||||||
| chrX:38621263
|
C | T | 1 | a0001c0001t0001g0056 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.82-44858C>T | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38621263 | ||||||
| chrX:38621268
|
T | C | 49 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(46): Show | 51 | HG00609.hp1 HG00621.hp1 HG00741.hp1 others(48): Show |
intron_variant | MODIFIER | c.82-44853T>C | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38621268 | ||||||
| chrX:38621728
|
C | CATTT | 176 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(173): Show | 181 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(178): Show |
intron_variant | MODIFIER | c.82-44393_82-44392i others(6): Show |
TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38621728 | ||||||
| chrX:38621805
|
G | A | 1 | a0001c0001t0001g0171 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.82-44316G>A | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38621805 | ||||||
| chrX:38621856
|
T | C | 1 | a0001c0001t0002g0155 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.82-44265T>C | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38621856 | ||||||
| chrX:38621926
|
A | C | 1 | a0001c0001t0002g0020 | 1 | NA19055.hp1 | intron_variant | MODIFIER | c.82-44195A>C | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38621926 | ||||||
| chrX:38621986
|
G | A | 4 | a0001c0001t0001g0089a0001c0001t0001g0187a0001c0001t0002g0080others(1): Show | 4 | HG01884.hp1 HG03471.hp1 NA18906.hp1 others(1): Show |
intron_variant | MODIFIER | c.82-44135G>A | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38621986 | ||||||
| chrX:38622003
|
C | T | 8 | a0001c0001t0001g0077a0001c0001t0001g0084a0001c0001t0001g0199others(5): Show | 8 | HG02559.hp1 HG02615.hp1 HG02615.hp2 others(5): Show |
intron_variant | MODIFIER | c.82-44118C>T | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38622003 | ||||||
| chrX:38622180
|
T | C | 8 | a0001c0001t0001g0077a0001c0001t0001g0084a0001c0001t0001g0199others(5): Show | 8 | HG02559.hp1 HG02615.hp1 HG02615.hp2 others(5): Show |
intron_variant | MODIFIER | c.82-43941T>C | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38622180 | ||||||
| chrX:38622320
|
G | A | 1 | a0001c0001t0001g0075 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.82-43801G>A | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38622320 | ||||||
| chrX:38622543
|
G | A | 186 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(183): Show | 192 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(189): Show |
intron_variant | MODIFIER | c.82-43578G>A | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38622543 | ||||||
| chrX:38622550
|
C | T | 2 | a0001c0001t0001g0090a0001c0001t0001g0091 | 2 | HG02572.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.82-43571C>T | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38622550 | ||||||
| chrX:38622647
|
G | C | 1 | a0001c0001t0001g0045 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.82-43474G>C | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38622647 | ||||||
| chrX:38622672
|
T | G | 1 | a0001c0001t0001g0187 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.82-43449T>G | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38622672 | ||||||
| chrX:38622679
|
C | T | 1 | a0001c0001t0001g0051 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.82-43442C>T | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38622679 | ||||||
| chrX:38622729
|
G | A | 12 | a0001c0001t0001g0054a0001c0001t0001g0056a0001c0001t0001g0059others(9): Show | 12 | HG01255.hp1 HG02055.hp1 HG02258.hp1 others(9): Show |
intron_variant | MODIFIER | c.82-43392G>A | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38622729 | ||||||
| chrX:38622730
|
C | A | 12 | a0001c0001t0001g0054a0001c0001t0001g0056a0001c0001t0001g0059others(9): Show | 12 | HG01255.hp1 HG02055.hp1 HG02258.hp1 others(9): Show |
intron_variant | MODIFIER | c.82-43391C>A | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38622730 | ||||||
| chrX:38622736
|
A | G | 85 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(82): Show | 88 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(85): Show |
intron_variant | MODIFIER | c.82-43385A>G | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38622736 | ||||||
| chrX:38622751
|
C | A | 1 | a0001c0001t0002g0013 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.82-43370C>A | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38622751 | ||||||
| chrX:38622802
|
G | A | 1 | a0001c0001t0001g0089 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.82-43319G>A | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38622802 | ||||||
| chrX:38622899
|
A | T | 1 | a0001c0001t0001g0054 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.82-43222A>T | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38622899 | ||||||
| chrX:38622937
|
C | T | 1 | a0001c0001t0001g0075 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.82-43184C>T | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38622937 | ||||||
| chrX:38623051
|
G | A | 13 | a0001c0001t0001g0108a0001c0001t0002g0022a0001c0001t0002g0028others(10): Show | 13 | HG01243.hp1 HG02109.hp2 HG02257.hp1 others(10): Show |
intron_variant | MODIFIER | c.82-43070G>A | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38623051 | ||||||
| chrX:38623269
|
A | G | 2 | a0001c0001t0001g0083a0001c0001t0002g0081 | 2 | HG01891.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.82-42852A>G | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38623269 | ||||||
| chrX:38623302
|
C | G | 2 | a0001c0001t0001g0083a0001c0001t0002g0081 | 2 | HG01891.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.82-42819C>G | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38623302 | ||||||
| chrX:38623407
|
C | T | 2 | a0001c0001t0001g0083a0001c0001t0002g0081 | 2 | HG01891.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.82-42714C>T | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38623407 | ||||||
| chrX:38623471
|
G | C | 170 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(167): Show | 175 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(172): Show |
intron_variant | MODIFIER | c.82-42650G>C | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38623471 | ||||||
| chrX:38623622
|
G | GT | 48 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(45): Show | 50 | HG00609.hp1 HG00741.hp1 HG01106.hp1 others(47): Show |
intron_variant | MODIFIER | c.82-42491dupT | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 38623622 | |||||
| chrX:38623622
|
G | GTT | 1 | a0001c0001t0001g0038 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.82-42492_82-42491d others(4): Show |
TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 38623622 | |||||
| chrX:38623822
|
G | T | 1 | a0001c0003t0001g0201 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.82-42299G>T | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38623822 | ||||||
| chrX:38623833
|
T | C | 159 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(156): Show | 164 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(161): Show |
intron_variant | MODIFIER | c.82-42288T>C | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38623833 | ||||||
| chrX:38623927
|
G | C | 23 | a0001c0001t0001g0056a0001c0001t0001g0059a0001c0001t0001g0071others(20): Show | 24 | HG01243.hp1 HG01255.hp1 HG01884.hp2 others(21): Show |
intron_variant | MODIFIER | c.82-42194G>C | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38623927 | ||||||
| chrX:38624069
|
G | A | 210 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(207): Show | 217 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(214): Show |
intron_variant | MODIFIER | c.82-42052G>A | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38624069 | ||||||
| chrX:38624239
|
G | C | 1 | a0001c0001t0001g0073 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.82-41882G>C | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38624239 | ||||||
| chrX:38624298
|
A | G | 173 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(170): Show | 178 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(175): Show |
intron_variant | MODIFIER | c.82-41823A>G | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38624298 | ||||||
| chrX:38624663
|
C | G | 1 | a0001c0001t0001g0177 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.82-41458C>G | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38624663 | ||||||
| chrX:38624679
|
T | C | 111 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(108): Show | 115 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(112): Show |
intron_variant | MODIFIER | c.82-41442T>C | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38624679 | ||||||
| chrX:38624680
|
T | A | 111 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(108): Show | 115 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(112): Show |
intron_variant | MODIFIER | c.82-41441T>A | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38624680 | ||||||
| chrX:38624742
|
C | A | 160 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(157): Show | 165 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(162): Show |
intron_variant | MODIFIER | c.82-41379C>A | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38624742 | ||||||
| chrX:38625062
|
C | T | 2 | a0001c0001t0001g0073a0001c0001t0001g0082 | 2 | HG01255.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.82-41059C>T | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38625062 | ||||||
| chrX:38625150
|
TC | T | 1 | a0001c0001t0002g0020 | 1 | NA19055.hp1 | intron_variant | MODIFIER | c.82-40968delC | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 38625150 | |||||
| chrX:38625286
|
CT | C | 1 | a0001c0001t0002g0020 | 1 | NA19055.hp1 | intron_variant | MODIFIER | c.82-40831delT | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 38625286 | |||||
| chrX:38625351
|
G | A | 3 | a0001c0001t0001g0084a0001c0001t0001g0210a0001c0001t0001g0211 | 3 | HG02615.hp1 HG02723.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.82-40770G>A | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38625351 | ||||||
| chrX:38625410
|
GGTTCTAG others(18): Show |
G | 1 | a0001c0001t0001g0118 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.82-40708_82-40684d others(27): Show |
TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 38625410 | |||||
| chrX:38625431
|
C | CAGA | 1 | a0001c0001t0002g0020 | 1 | NA19055.hp1 | intron_variant | MODIFIER | c.82-40687_82-40685d others(5): Show |
TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 38625431 | |||||
| chrX:38625679
|
T | A | 1 | a0001c0001t0001g0137 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.82-40442T>A | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38625679 | ||||||
| chrX:38625725
|
T | A | 112 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(109): Show | 116 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(113): Show |
intron_variant | MODIFIER | c.82-40396T>A | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38625725 | ||||||
| chrX:38626220
|
GT | G | 215 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(212): Show | 222 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(219): Show |
intron_variant | MODIFIER | c.82-39898delT | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 38626220 | |||||
| chrX:38626585
|
G | T | 8 | a0001c0001t0001g0077a0001c0001t0001g0084a0001c0001t0001g0199others(5): Show | 8 | HG02559.hp1 HG02615.hp1 HG02615.hp2 others(5): Show |
intron_variant | MODIFIER | c.82-39536G>T | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38626585 | ||||||
| chrX:38626623
|
TG | T | 1 | a0001c0001t0002g0020 | 1 | NA19055.hp1 | intron_variant | MODIFIER | c.82-39495delG | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 38626623 | |||||
| chrX:38626628
|
A | G | 1 | a0001c0001t0001g0168 | 1 | NA19004.hp1 | intron_variant | MODIFIER | c.82-39493A>G | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38626628 | ||||||
| chrX:38626713
|
G | A | 12 | a0001c0001t0001g0059a0001c0001t0001g0071a0001c0001t0001g0072others(9): Show | 12 | HG01255.hp1 HG02055.hp1 HG02258.hp1 others(9): Show |
intron_variant | MODIFIER | c.82-39408G>A | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38626713 | ||||||
| chrX:38626738
|
C | A | 2 | a0001c0001t0001g0023a0001c0003t0001g0066 | 2 | HG02965.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.82-39383C>A | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38626738 | ||||||
| chrX:38626836
|
G | A | 1 | a0001c0001t0002g0021 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.82-39285G>A | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38626836 | ||||||
| chrX:38627173
|
G | A | 33 | a0001c0001t0001g0014a0001c0001t0001g0029a0001c0001t0001g0038others(30): Show | 33 | HG00621.hp1 HG01106.hp1 HG01934.hp1 others(30): Show |
intron_variant | MODIFIER | c.82-38948G>A | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38627173 | ||||||
| chrX:38627359
|
G | A | 2 | a0001c0001t0002g0016a0001c0001t0002g0017 | 2 | NA18948.hp1 NA18977.hp1 |
intron_variant | MODIFIER | c.82-38762G>A | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38627359 | ||||||
| chrX:38627366
|
C | T | 9 | a0001c0001t0001g0075a0001c0001t0002g0022a0001c0001t0002g0065others(6): Show | 9 | HG02257.hp1 HG02630.hp2 HG02809.hp2 others(6): Show |
intron_variant | MODIFIER | c.82-38755C>T | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38627366 | ||||||
| chrX:38627572
|
C | T | 1 | a0001c0001t0002g0080 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.82-38549C>T | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38627572 | ||||||
| chrX:38627693
|
AC | A | 1 | a0001c0001t0002g0020 | 1 | NA19055.hp1 | intron_variant | MODIFIER | c.82-38425delC | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 38627693 | |||||
| chrX:38627772
|
G | A | 8 | a0001c0001t0001g0077a0001c0001t0001g0084a0001c0001t0001g0199others(5): Show | 8 | HG02559.hp1 HG02615.hp1 HG02615.hp2 others(5): Show |
intron_variant | MODIFIER | c.82-38349G>A | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38627772 | ||||||
| chrX:38627853
|
C | T | 11 | a0001c0001t0001g0056a0001c0001t0001g0075a0001c0001t0001g0202others(8): Show | 11 | HG02257.hp1 HG02630.hp2 HG02809.hp2 others(8): Show |
intron_variant | MODIFIER | c.82-38268C>T | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38627853 | ||||||
| chrX:38628126
|
G | A | 113 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(110): Show | 117 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(114): Show |
intron_variant | MODIFIER | c.82-37995G>A | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38628126 | ||||||
| chrX:38628336
|
G | A | 113 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(110): Show | 117 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(114): Show |
intron_variant | MODIFIER | c.82-37785G>A | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38628336 | ||||||
| chrX:38628336
|
G | GT | 1 | a0001c0001t0001g0014 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.82-37776dupT | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 38628336 | |||||
| chrX:38628358
|
G | A | 1 | a0001c0003t0001g0181 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.82-37763G>A | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38628358 | ||||||
| chrX:38628465
|
C | T | 1 | a0001c0001t0001g0169 | 1 | NA18991.hp2 | intron_variant | MODIFIER | c.82-37656C>T | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38628465 | ||||||
| chrX:38628466
|
G | A | 2 | a0001c0001t0002g0028a0001c0001t0002g0191 | 2 | HG02922.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.82-37655G>A | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38628466 | ||||||
| chrX:38628543
|
C | T | 2 | a0001c0002t0001g0212a0001c0002t0001g0213 | 2 | HG03195.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.82-37578C>T | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38628543 | ||||||
| chrX:38628600
|
C | T | 2 | a0001c0001t0001g0059a0001c0001t0001g0071 | 2 | HG02895.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.82-37521C>T | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38628600 | ||||||
| chrX:38628726
|
AT | A | 1 | a0001c0001t0002g0020 | 1 | NA19055.hp1 | intron_variant | MODIFIER | c.82-37392delT | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 38628726 | |||||
| chrX:38628757
|
CACATTT | C | 2 | a0001c0001t0001g0083a0001c0001t0002g0081 | 2 | HG01891.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.82-37361_82-37356d others(8): Show |
TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 38628757 | |||||
| chrX:38628862
|
AT | A | 1 | a0001c0001t0002g0020 | 1 | NA19055.hp1 | intron_variant | MODIFIER | c.82-37254delT | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 38628862 | |||||
| chrX:38629076
|
A | G | 1 | a0001c0001t0002g0021 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.82-37045A>G | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38629076 | ||||||
| chrX:38629265
|
C | T | 2 | a0001c0001t0001g0023a0001c0003t0001g0066 | 2 | HG02965.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.82-36856C>T | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38629265 | ||||||
| chrX:38629357
|
A | G | 1 | a0001c0001t0002g0102 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.82-36764A>G | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38629357 | ||||||
| chrX:38629376
|
A | G | 2 | a0001c0001t0001g0083a0001c0001t0002g0081 | 2 | HG01891.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.82-36745A>G | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38629376 | ||||||
| chrX:38629481
|
C | G | 1 | a0001c0001t0002g0013 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.82-36640C>G | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38629481 | ||||||
| chrX:38629772
|
G | GA | 1 | a0001c0001t0001g0014 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.82-36342dupA | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 38629772 | |||||
| chrX:38630005
|
T | C | 1 | a0001c0001t0002g0021 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.82-36116T>C | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38630005 | ||||||
| chrX:38630059
|
A | G | 2 | a0001c0001t0001g0023a0001c0003t0001g0066 | 2 | HG02965.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.82-36062A>G | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38630059 | ||||||
| chrX:38630231
|
AT | A | 1 | a0001c0001t0002g0020 | 1 | NA19055.hp1 | intron_variant | MODIFIER | c.82-35886delT | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 38630231 | |||||
| chrX:38630290
|
T | C | 8 | a0001c0001t0001g0077a0001c0001t0001g0084a0001c0001t0001g0199others(5): Show | 8 | HG02559.hp1 HG02615.hp1 HG02615.hp2 others(5): Show |
intron_variant | MODIFIER | c.82-35831T>C | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38630290 | ||||||
| chrX:38630400
|
G | GT | 2 | a0001c0001t0001g0014a0001c0001t0001g0048 | 2 | NA18961.hp1 NA19083.hp1 |
intron_variant | MODIFIER | c.82-35713dupT | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 38630400 | |||||
| chrX:38630428
|
T | C | 2 | a0001c0002t0001g0212a0001c0002t0001g0213 | 2 | HG03195.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.82-35693T>C | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38630428 | ||||||
| chrX:38630479
|
G | A | 113 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(110): Show | 117 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(114): Show |
intron_variant | MODIFIER | c.82-35642G>A | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38630479 | ||||||
| chrX:38630590
|
A | G | 1 | a0001c0001t0001g0029 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.82-35531A>G | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38630590 | ||||||
| chrX:38630849
|
A | G | 113 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(110): Show | 117 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(114): Show |
intron_variant | MODIFIER | c.82-35272A>G | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38630849 | ||||||
| chrX:38630975
|
A | G | 1 | a0001c0001t0001g0148 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.82-35146A>G | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38630975 | ||||||
| chrX:38631007
|
CA | C | 1 | a0001c0002t0001g0092 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.82-35111delA | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 38631007 | |||||
| chrX:38631288
|
C | T | 6 | a0001c0001t0001g0077a0001c0001t0001g0084a0001c0001t0001g0199others(3): Show | 6 | HG02559.hp1 HG02615.hp1 HG02647.hp1 others(3): Show |
intron_variant | MODIFIER | c.82-34833C>T | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38631288 | ||||||
| chrX:38631309
|
C | T | 1 | a0001c0001t0001g0147 | 1 | NA19006.hp1 | intron_variant | MODIFIER | c.82-34812C>T | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38631309 | ||||||
| chrX:38631364
|
TA | T | 1 | a0001c0001t0002g0020 | 1 | NA19055.hp1 | intron_variant | MODIFIER | c.82-34750delA | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 38631364 | |||||
| chrX:38631442
|
G | A | 8 | a0001c0001t0001g0077a0001c0001t0001g0084a0001c0001t0001g0199others(5): Show | 8 | HG02559.hp1 HG02615.hp1 HG02615.hp2 others(5): Show |
intron_variant | MODIFIER | c.82-34679G>A | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38631442 | ||||||
| chrX:38631591
|
A | G | 113 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(110): Show | 117 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(114): Show |
intron_variant | MODIFIER | c.82-34530A>G | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38631591 | ||||||
| chrX:38631592
|
C | T | 8 | a0001c0001t0001g0077a0001c0001t0001g0084a0001c0001t0001g0199others(5): Show | 8 | HG02559.hp1 HG02615.hp1 HG02615.hp2 others(5): Show |
intron_variant | MODIFIER | c.82-34529C>T | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38631592 | ||||||
| chrX:38631608
|
TC | T | 1 | a0001c0001t0002g0020 | 1 | NA19055.hp1 | intron_variant | MODIFIER | c.82-34510delC | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 38631608 | |||||
| chrX:38632016
|
A | AT | 2 | a0001c0001t0001g0115a0001c0001t0001g0166 | 2 | NA18940.hp1 NA18967.hp1 |
intron_variant | MODIFIER | c.82-34095dupT | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 38632016 | |||||
| chrX:38632016
|
AT | A | 1 | a0001c0001t0002g0020 | 1 | NA19055.hp1 | intron_variant | MODIFIER | c.82-34095delT | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 38632016 | |||||
| chrX:38632294
|
A | C | 1 | a0001c0001t0001g0071 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.82-33827A>C | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38632294 | ||||||
| chrX:38632450
|
G | A | 1 | a0001c0001t0002g0021 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.82-33671G>A | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38632450 | ||||||
| chrX:38632616
|
T | C | 1 | a0001c0001t0002g0183 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.82-33505T>C | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38632616 | ||||||
| chrX:38632839
|
A | G | 1 | a0001c0001t0001g0091 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.82-33282A>G | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38632839 | ||||||
| chrX:38634238
|
C | T | 38 | a0001c0001t0001g0014a0001c0001t0001g0029a0001c0001t0001g0038others(35): Show | 38 | HG00621.hp1 HG01106.hp1 HG01175.hp2 others(35): Show |
intron_variant | MODIFIER | c.82-31883C>T | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38634238 | ||||||
| chrX:38634861
|
G | A | 169 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(166): Show | 174 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(171): Show |
intron_variant | MODIFIER | c.82-31260G>A | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38634861 | ||||||
| chrX:38634917
|
AG | A | 1 | a0001c0001t0002g0097 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.82-31201delG | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 38634917 | |||||
| chrX:38635002
|
GC | G | 5 | a0001c0001t0001g0089a0001c0001t0001g0091a0001c0001t0001g0187others(2): Show | 5 | HG01884.hp1 HG03130.hp1 HG03471.hp1 others(2): Show |
intron_variant | MODIFIER | c.82-31115delC | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 38635002 | |||||
| chrX:38635247
|
G | A | 6 | a0001c0001t0001g0077a0001c0001t0001g0084a0001c0001t0001g0199others(3): Show | 6 | HG02559.hp1 HG02615.hp1 HG02647.hp1 others(3): Show |
intron_variant | MODIFIER | c.82-30874G>A | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38635247 | ||||||
| chrX:38635483
|
G | C | 8 | a0001c0001t0001g0077a0001c0001t0001g0084a0001c0001t0001g0199others(5): Show | 8 | HG02559.hp1 HG02615.hp1 HG02615.hp2 others(5): Show |
intron_variant | MODIFIER | c.82-30638G>C | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38635483 | ||||||
| chrX:38635813
|
G | A | 68 | a0001c0001t0001g0014a0001c0001t0001g0023a0001c0001t0001g0029others(65): Show | 69 | HG00621.hp1 HG01106.hp1 HG01175.hp2 others(66): Show |
intron_variant | MODIFIER | c.82-30308G>A | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38635813 | ||||||
| chrX:38635940
|
C | A | 1 | a0001c0001t0001g0047 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.82-30181C>A | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38635940 | ||||||
| chrX:38636060
|
G | GT | 1 | a0002c0004t0001g0173 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.82-30053dupT | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 38636060 | |||||
| chrX:38636066
|
T | C | 5 | a0001c0001t0001g0089a0001c0001t0001g0091a0001c0001t0001g0187others(2): Show | 5 | HG01884.hp1 HG03130.hp1 HG03471.hp1 others(2): Show |
intron_variant | MODIFIER | c.82-30055T>C | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38636066 | ||||||
| chrX:38636075
|
G | GTTAT | 40 | a0001c0001t0001g0010a0001c0001t0001g0014a0001c0001t0001g0029others(37): Show | 41 | HG01106.hp1 HG01167.hp1 HG01169.hp1 others(38): Show |
intron_variant | MODIFIER | c.82-30015_82-30012d others(6): Show |
TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 38636075 | |||||
| chrX:38636075
|
G | GTTATTTA others(1): Show |
15 | a0001c0001t0001g0023a0001c0001t0001g0038a0001c0001t0001g0056others(12): Show | 15 | HG00621.hp1 HG01884.hp2 HG02109.hp2 others(12): Show |
intron_variant | MODIFIER | c.82-30019_82-30012d others(10): Show |
TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 38636075 | |||||
| chrX:38636075
|
G | GTTATTTA others(5): Show |
3 | a0001c0001t0001g0075a0001c0001t0002g0021a0001c0001t0002g0081 | 3 | HG03209.hp1 NA19043.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.82-30023_82-30012d others(14): Show |
TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 38636075 | |||||
| chrX:38636075
|
G | GTTATTTA others(9): Show |
1 | a0001c0001t0001g0083 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.82-30027_82-30012d others(18): Show |
TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 38636075 | |||||
| chrX:38636075
|
GTTAT | G | 109 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(106): Show | 113 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(110): Show |
intron_variant | MODIFIER | c.82-30015_82-30012d others(6): Show |
TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 38636075 | |||||
| chrX:38636075
|
GTTATTTA others(1): Show |
G | 1 | a0001c0001t0005g0078 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.82-30019_82-30012d others(10): Show |
TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 38636075 | |||||
| chrX:38636329
|
C | T | 1 | a0002c0004t0001g0173 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.82-29792C>T | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38636329 | ||||||
| chrX:38636472
|
A | T | 1 | a0001c0001t0001g0125 | 1 | NA18988.hp1 | intron_variant | MODIFIER | c.82-29649A>T | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38636472 | ||||||
| chrX:38636697
|
A | G | 2 | a0001c0001t0001g0023a0001c0003t0001g0066 | 2 | HG02965.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.82-29424A>G | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38636697 | ||||||
| chrX:38636734
|
C | T | 8 | a0001c0001t0002g0022a0001c0001t0002g0065a0001c0001t0002g0067others(5): Show | 8 | HG02257.hp1 HG02630.hp2 HG02809.hp2 others(5): Show |
intron_variant | MODIFIER | c.82-29387C>T | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38636734 | ||||||
| chrX:38636737
|
G | A | 1 | a0001c0001t0002g0032 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.82-29384G>A | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38636737 | ||||||
| chrX:38636758
|
C | A | 1 | a0001c0001t0001g0072 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.82-29363C>A | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38636758 | ||||||
| chrX:38636851
|
T | C | 1 | a0001c0001t0001g0041 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.82-29270T>C | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38636851 | ||||||
| chrX:38636941
|
C | T | 1 | a0001c0001t0001g0075 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.82-29180C>T | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38636941 | ||||||
| chrX:38637046
|
C | T | 174 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(171): Show | 179 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(176): Show |
intron_variant | MODIFIER | c.82-29075C>T | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38637046 | ||||||
| chrX:38637048
|
A | G | 8 | a0001c0001t0002g0022a0001c0001t0002g0065a0001c0001t0002g0067others(5): Show | 8 | HG02257.hp1 HG02630.hp2 HG02809.hp2 others(5): Show |
intron_variant | MODIFIER | c.82-29073A>G | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38637048 | ||||||
| chrX:38637065
|
C | G | 1 | a0001c0001t0001g0177 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.82-29056C>G | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38637065 | ||||||
| chrX:38637074
|
A | G | 1 | a0001c0001t0001g0026 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.82-29047A>G | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38637074 | ||||||
| chrX:38637367
|
G | A | 4 | a0001c0001t0001g0203a0001c0001t0001g0204a0001c0001t0001g0205others(1): Show | 4 | HG02109.hp1 HG02145.hp1 HG02630.hp1 others(1): Show |
intron_variant | MODIFIER | c.82-28754G>A | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38637367 | ||||||
| chrX:38637421
|
T | G | 33 | a0001c0001t0001g0014a0001c0001t0001g0029a0001c0001t0001g0038others(30): Show | 33 | HG00621.hp1 HG01106.hp1 HG01175.hp2 others(30): Show |
intron_variant | MODIFIER | c.82-28700T>G | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38637421 | ||||||
| chrX:38637609
|
C | A | 104 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(101): Show | 108 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(105): Show |
intron_variant | MODIFIER | c.82-28512C>A | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38637609 | ||||||
| chrX:38637846
|
AT | A | 1 | a0001c0001t0002g0021 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.82-28274delT | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38637846 | ||||||
| chrX:38638006
|
A | G | 1 | a0001c0001t0002g0021 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.82-28115A>G | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38638006 | ||||||
| chrX:38638035
|
GAA | G | 5 | a0001c0001t0001g0089a0001c0001t0001g0091a0001c0001t0001g0187others(2): Show | 5 | HG01884.hp1 HG03130.hp1 HG03471.hp1 others(2): Show |
intron_variant | MODIFIER | c.82-28084_82-28083d others(4): Show |
TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 38638035 | |||||
| chrX:38638297
|
C | T | 2 | a0001c0001t0001g0023a0001c0003t0001g0066 | 2 | HG02965.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.82-27824C>T | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38638297 | ||||||
| chrX:38638655
|
A | C | 1 | a0001c0001t0001g0082 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.82-27466A>C | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38638655 | ||||||
| chrX:38638657
|
C | A | 10 | a0001c0001t0001g0056a0001c0001t0001g0202a0001c0001t0002g0022others(7): Show | 10 | HG02257.hp1 HG02630.hp2 HG02809.hp2 others(7): Show |
intron_variant | MODIFIER | c.82-27464C>A | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38638657 | ||||||
| chrX:38638819
|
G | A | 1 | a0001c0001t0001g0046 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.82-27302G>A | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38638819 | ||||||
| chrX:38638873
|
CT | C | 104 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(101): Show | 108 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(105): Show |
intron_variant | MODIFIER | c.82-27244delT | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 38638873 | |||||
| chrX:38638889
|
A | G | 1 | a0001c0001t0001g0014 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.82-27232A>G | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38638889 | ||||||
| chrX:38638924
|
TG | T | 1 | a0001c0001t0001g0134 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.82-27193delG | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 38638924 | |||||
| chrX:38639216
|
T | A | 1 | a0001c0001t0001g0134 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.82-26905T>A | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38639216 | ||||||
| chrX:38639252
|
G | A | 2 | a0001c0002t0001g0212a0001c0002t0001g0213 | 2 | HG03195.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.82-26869G>A | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38639252 | ||||||
| chrX:38639610
|
C | T | 1 | a0001c0001t0002g0150 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.82-26511C>T | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38639610 | ||||||
| chrX:38639680
|
C | T | 1 | a0001c0001t0002g0031 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.82-26441C>T | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38639680 | ||||||
| chrX:38639692
|
G | T | 10 | a0001c0001t0001g0023a0001c0001t0002g0022a0001c0001t0002g0065others(7): Show | 10 | HG02257.hp1 HG02630.hp2 HG02809.hp2 others(7): Show |
intron_variant | MODIFIER | c.82-26429G>T | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38639692 | ||||||
| chrX:38640173
|
G | A | 1 | a0001c0001t0002g0183 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.82-25948G>A | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38640173 | ||||||
| chrX:38640315
|
C | T | 2 | a0001c0001t0001g0075a0001c0001t0002g0021 | 2 | NA19043.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.82-25806C>T | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38640315 | ||||||
| chrX:38640809
|
C | T | 2 | a0001c0001t0001g0077a0001c0001t0001g0199 | 2 | HG02559.hp1 HG02647.hp1 |
intron_variant | MODIFIER | c.82-25312C>T | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38640809 | ||||||
| chrX:38640834
|
A | G | 2 | a0001c0001t0001g0010a0001c0001t0001g0011 | 2 | HG01074.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.82-25287A>G | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38640834 | ||||||
| chrX:38640835
|
A | T | 174 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(171): Show | 179 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(176): Show |
intron_variant | MODIFIER | c.82-25286A>T | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38640835 | ||||||
| chrX:38640902
|
G | A | 4 | a0001c0001t0001g0059a0001c0001t0001g0071a0001c0001t0001g0072others(1): Show | 4 | HG02055.hp1 HG02895.hp1 HG06807.hp1 others(1): Show |
intron_variant | MODIFIER | c.82-25219G>A | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38640902 | ||||||
| chrX:38641076
|
G | GT | 1 | a0001c0001t0002g0019 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.82-25044dupT | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 38641076 | |||||
| chrX:38641121
|
C | T | 10 | a0001c0001t0001g0056a0001c0001t0001g0202a0001c0001t0002g0022others(7): Show | 10 | HG02257.hp1 HG02630.hp2 HG02809.hp2 others(7): Show |
intron_variant | MODIFIER | c.82-25000C>T | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38641121 | ||||||
| chrX:38641255
|
C | T | 102 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(99): Show | 106 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(103): Show |
intron_variant | MODIFIER | c.82-24866C>T | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38641255 | ||||||
| chrX:38641405
|
G | A | 1 | a0001c0001t0002g0117 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.82-24716G>A | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38641405 | ||||||
| chrX:38641425
|
C | T | 5 | a0001c0001t0001g0089a0001c0001t0001g0091a0001c0001t0001g0187others(2): Show | 5 | HG01884.hp1 HG03130.hp1 HG03471.hp1 others(2): Show |
intron_variant | MODIFIER | c.82-24696C>T | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38641425 | ||||||
| chrX:38641439
|
A | T | 1 | a0001c0001t0001g0187 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.82-24682A>T | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38641439 | ||||||
| chrX:38641483
|
G | A | 1 | a0001c0001t0003g0079 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.82-24638G>A | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38641483 | ||||||
| chrX:38641771
|
GC | G | 1 | a0001c0001t0002g0019 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.82-24348delC | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 38641771 | |||||
| chrX:38642152
|
CCA | C | 2 | a0001c0001t0001g0075a0001c0001t0002g0021 | 2 | NA19043.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.82-23968_82-23967d others(4): Show |
TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38642152 | ||||||
| chrX:38642235
|
G | T | 68 | a0001c0001t0001g0014a0001c0001t0001g0023a0001c0001t0001g0029others(65): Show | 69 | HG00621.hp1 HG01106.hp1 HG01175.hp2 others(66): Show |
intron_variant | MODIFIER | c.82-23886G>T | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38642235 | ||||||
| chrX:38642243
|
A | AG | 1 | a0001c0001t0002g0019 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.82-23875dupG | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 38642243 | |||||
| chrX:38642394
|
G | A | 2 | a0001c0003t0001g0181a0001c0003t0001g0215 | 2 | HG02258.hp1 HG02622.hp1 |
intron_variant | MODIFIER | c.82-23727G>A | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38642394 | ||||||
| chrX:38642455
|
A | T | 10 | a0001c0001t0001g0075a0001c0001t0001g0077a0001c0001t0001g0084others(7): Show | 10 | HG02559.hp1 HG02615.hp1 HG02615.hp2 others(7): Show |
intron_variant | MODIFIER | c.82-23666A>T | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38642455 | ||||||
| chrX:38642752
|
TC | T | 1 | a0001c0001t0002g0019 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.82-23366delC | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 38642752 | |||||
| chrX:38642875
|
G | A | 31 | a0001c0001t0001g0014a0001c0001t0001g0029a0001c0001t0001g0038others(28): Show | 31 | HG00621.hp1 HG01106.hp1 HG01175.hp2 others(28): Show |
intron_variant | MODIFIER | c.82-23246G>A | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38642875 | ||||||
| chrX:38642968
|
A | G | 2 | a0001c0001t0001g0089a0001c0001t0001g0187 | 2 | HG01884.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.82-23153A>G | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38642968 | ||||||
| chrX:38643057
|
TTAAATGT others(12): Show |
T | 1 | a0001c0001t0001g0115 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.82-23062_82-23044d others(21): Show |
TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 38643057 | |||||
| chrX:38643144
|
C | T | 4 | a0001c0001t0001g0089a0001c0001t0001g0187a0001c0001t0002g0080others(1): Show | 4 | HG01884.hp1 HG03471.hp1 NA18906.hp1 others(1): Show |
intron_variant | MODIFIER | c.82-22977C>T | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38643144 | ||||||
| chrX:38643145
|
G | A | 10 | a0001c0001t0001g0075a0001c0001t0001g0077a0001c0001t0001g0084others(7): Show | 10 | HG02559.hp1 HG02615.hp1 HG02615.hp2 others(7): Show |
intron_variant | MODIFIER | c.82-22976G>A | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38643145 | ||||||
| chrX:38643239
|
G | A | 1 | a0001c0001t0002g0080 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.82-22882G>A | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38643239 | ||||||
| chrX:38643336
|
G | A | 3 | a0001c0001t0001g0073a0001c0001t0001g0082a0001c0001t0001g0090 | 3 | HG01255.hp1 HG02572.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.82-22785G>A | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38643336 | ||||||
| chrX:38643672
|
C | CA | 10 | a0001c0001t0001g0077a0001c0001t0001g0087a0001c0001t0001g0199others(7): Show | 11 | HG01884.hp2 HG02109.hp2 HG02559.hp1 others(8): Show |
intron_variant | MODIFIER | c.82-22426dupA | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 38643672 | |||||
| chrX:38643672
|
C | CAA | 31 | a0001c0001t0001g0014a0001c0001t0001g0029a0001c0001t0001g0040others(28): Show | 31 | HG01175.hp2 HG01934.hp1 HG02056.hp1 others(28): Show |
intron_variant | MODIFIER | c.82-22427_82-22426d others(4): Show |
TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 38643672 | |||||
| chrX:38643672
|
C | CAAA | 5 | a0001c0001t0001g0103a0001c0001t0001g0137a0001c0001t0002g0017others(2): Show | 5 | HG01106.hp1 NA18948.hp1 NA18971.hp1 others(2): Show |
intron_variant | MODIFIER | c.82-22428_82-22426d others(5): Show |
TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 38643672 | |||||
| chrX:38643672
|
C | CAAAA | 1 | a0001c0001t0001g0038 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.82-22429_82-22426d others(6): Show |
TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 38643672 | |||||
| chrX:38643672
|
CA | C | 99 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(96): Show | 102 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(99): Show |
intron_variant | MODIFIER | c.82-22426delA | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 38643672 | |||||
| chrX:38643672
|
CAA | C | 6 | a0001c0001t0001g0089a0001c0001t0001g0090a0001c0001t0001g0091others(3): Show | 6 | HG01884.hp1 HG02572.hp1 HG03130.hp1 others(3): Show |
intron_variant | MODIFIER | c.82-22427_82-22426d others(4): Show |
TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 38643672 | |||||
| chrX:38643672
|
CAAAAAAA | C | 2 | a0001c0001t0001g0007a0001c0001t0001g0193 | 3 | NA18965.hp1 NA18966.hp1 NA18986.hp1 |
intron_variant | MODIFIER | c.82-22432_82-22426d others(9): Show |
TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 38643672 | |||||
| chrX:38643824
|
G | A | 1 | a0001c0001t0002g0208 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.82-22297G>A | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38643824 | ||||||
| chrX:38643850
|
A | G | 10 | a0001c0001t0001g0075a0001c0001t0001g0077a0001c0001t0001g0084others(7): Show | 10 | HG02559.hp1 HG02615.hp1 HG02615.hp2 others(7): Show |
intron_variant | MODIFIER | c.82-22271A>G | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38643850 | ||||||
| chrX:38643869
|
C | T | 160 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(157): Show | 165 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(162): Show |
intron_variant | MODIFIER | c.82-22252C>T | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38643869 | ||||||
| chrX:38643918
|
A | G | 1 | a0001c0001t0002g0013 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.82-22203A>G | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38643918 | ||||||
| chrX:38644005
|
C | T | 1 | a0001c0001t0001g0075 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.82-22116C>T | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38644005 | ||||||
| chrX:38644053
|
G | T | 1 | a0001c0001t0001g0047 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.82-22068G>T | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38644053 | ||||||
| chrX:38644098
|
T | C | 1 | a0001c0001t0001g0054 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.82-22023T>C | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38644098 | ||||||
| chrX:38644169
|
G | T | 1 | a0001c0001t0001g0091 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.82-21952G>T | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38644169 | ||||||
| chrX:38644391
|
C | A | 1 | a0001c0001t0001g0125 | 1 | NA18988.hp1 | intron_variant | MODIFIER | c.82-21730C>A | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38644391 | ||||||
| chrX:38644584
|
G | A | 1 | a0001c0001t0001g0105 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.82-21537G>A | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38644584 | ||||||
| chrX:38644604
|
G | A | 2 | a0001c0001t0001g0046a0001c0001t0001g0113 | 2 | NA18952.hp1 NA18994.hp1 |
intron_variant | MODIFIER | c.82-21517G>A | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38644604 | ||||||
| chrX:38644909
|
A | C | 1 | a0001c0001t0001g0041 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.82-21212A>C | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38644909 | ||||||
| chrX:38644936
|
G | A | 2 | a0001c0002t0001g0212a0001c0002t0001g0213 | 2 | HG03195.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.82-21185G>A | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38644936 | ||||||
| chrX:38645360
|
G | A | 12 | a0001c0001t0001g0023a0001c0001t0001g0083a0001c0001t0002g0022others(9): Show | 12 | HG01891.hp2 HG02257.hp1 HG02630.hp2 others(9): Show |
intron_variant | MODIFIER | c.82-20761G>A | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38645360 | ||||||
| chrX:38645553
|
G | GA | 17 | a0001c0001t0001g0056a0001c0001t0001g0077a0001c0001t0001g0084others(14): Show | 18 | HG01884.hp2 HG02109.hp2 HG02559.hp1 others(15): Show |
intron_variant | MODIFIER | c.82-20556dupA | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 38645553 | |||||
| chrX:38645553
|
G | GAA | 1 | a0001c0001t0001g0075 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.82-20557_82-20556d others(4): Show |
TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 38645553 | |||||
| chrX:38645553
|
GA | G | 1 | a0001c0001t0001g0187 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.82-20556delA | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 38645553 | |||||
| chrX:38645685
|
C | T | 1 | a0001c0001t0001g0083 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.82-20436C>T | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38645685 | ||||||
| chrX:38645918
|
T | TA | 43 | a0001c0001t0001g0014a0001c0001t0001g0029a0001c0001t0001g0038others(40): Show | 44 | HG00621.hp1 HG01106.hp1 HG01175.hp2 others(41): Show |
intron_variant | MODIFIER | c.82-20202dupA | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 38645918 | |||||
| chrX:38646132
|
T | C | 1 | a0001c0002t0001g0088 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.82-19989T>C | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38646132 | ||||||
| chrX:38646146
|
T | TA | 2 | a0001c0001t0001g0107a0001c0001t0001g0125 | 2 | NA18988.hp1 NA19082.hp1 |
intron_variant | MODIFIER | c.82-19965dupA | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 38646146 | |||||
| chrX:38646146
|
T | TAA | 1 | a0001c0002t0001g0074 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.82-19966_82-19965d others(4): Show |
TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 38646146 | |||||
| chrX:38646146
|
T | TAAA | 9 | a0001c0001t0001g0075a0001c0001t0001g0077a0001c0001t0001g0084others(6): Show | 9 | HG02559.hp1 HG02615.hp1 HG02615.hp2 others(6): Show |
intron_variant | MODIFIER | c.82-19967_82-19965d others(5): Show |
TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 38646146 | |||||
| chrX:38646146
|
TA | T | 1 | a0001c0003t0001g0215 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.82-19965delA | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 38646146 | |||||
| chrX:38646239
|
T | C | 33 | a0001c0001t0001g0014a0001c0001t0001g0029a0001c0001t0001g0038others(30): Show | 33 | HG00621.hp1 HG01106.hp1 HG01175.hp2 others(30): Show |
intron_variant | MODIFIER | c.82-19882T>C | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38646239 | ||||||
| chrX:38646453
|
G | A | 3 | a0001c0001t0001g0073a0001c0001t0001g0082a0001c0001t0001g0090 | 3 | HG01255.hp1 HG02572.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.82-19668G>A | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38646453 | ||||||
| chrX:38646652
|
T | C | 1 | a0001c0001t0002g0021 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.82-19469T>C | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38646652 | ||||||
| chrX:38646700
|
T | TC | 1 | a0001c0001t0002g0019 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.82-19417dupC | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 38646700 | |||||
| chrX:38646749
|
T | G | 1 | a0001c0001t0001g0044 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.82-19372T>G | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38646749 | ||||||
| chrX:38646777
|
G | A | 1 | a0001c0001t0001g0071 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.82-19344G>A | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38646777 | ||||||
| chrX:38646832
|
TG | T | 1 | a0001c0001t0002g0019 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.82-19286delG | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 38646832 | |||||
| chrX:38646873
|
C | CG | 1 | a0001c0001t0002g0019 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.82-19245dupG | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 38646873 | |||||
| chrX:38646873
|
C | T | 9 | a0001c0001t0001g0075a0001c0001t0001g0077a0001c0001t0001g0084others(6): Show | 9 | HG02559.hp1 HG02615.hp1 HG02615.hp2 others(6): Show |
intron_variant | MODIFIER | c.82-19248C>T | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38646873 | ||||||
| chrX:38647208
|
C | CCT | 1 | a0001c0001t0002g0019 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.82-18912_82-18911i others(4): Show |
TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 38647208 | |||||
| chrX:38647272
|
T | C | 1 | a0001c0001t0001g0075 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.82-18849T>C | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38647272 | ||||||
| chrX:38647311
|
T | C | 1 | a0001c0001t0002g0081 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.82-18810T>C | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38647311 | ||||||
| chrX:38647406
|
C | T | 1 | a0001c0001t0001g0075 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.82-18715C>T | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38647406 | ||||||
| chrX:38647747
|
TG | T | 93 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(90): Show | 97 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(94): Show |
intron_variant | MODIFIER | c.82-18372delG | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 38647747 | |||||
| chrX:38647827
|
G | A | 6 | a0001c0001t0001g0077a0001c0001t0001g0084a0001c0001t0001g0199others(3): Show | 6 | HG02559.hp1 HG02615.hp1 HG02647.hp1 others(3): Show |
intron_variant | MODIFIER | c.82-18294G>A | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38647827 | ||||||
| chrX:38648091
|
T | TG | 1 | a0001c0001t0002g0019 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.82-18027dupG | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 38648091 | |||||
| chrX:38648191
|
T | C | 3 | a0001c0001t0001g0089a0001c0001t0005g0078a0001c0002t0001g0074 | 3 | HG02615.hp2 HG02717.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.82-17930T>C | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38648191 | ||||||
| chrX:38648193
|
A | G | 3 | a0001c0001t0001g0089a0001c0001t0005g0078a0001c0002t0001g0074 | 3 | HG02615.hp2 HG02717.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.82-17928A>G | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38648193 | ||||||
| chrX:38648279
|
T | C | 6 | a0001c0001t0001g0056a0001c0001t0001g0087a0001c0001t0001g0202others(3): Show | 7 | HG02559.hp2 HG02818.hp1 HG03195.hp1 others(4): Show |
intron_variant | MODIFIER | c.82-17842T>C | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38648279 | ||||||
| chrX:38648475
|
G | T | 1 | a0001c0001t0001g0180 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.82-17646G>T | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38648475 | ||||||
| chrX:38648503
|
G | C | 1 | a0001c0001t0001g0062 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.82-17618G>C | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38648503 | ||||||
| chrX:38648544
|
G | A | 1 | a0001c0001t0001g0125 | 1 | NA18988.hp1 | intron_variant | MODIFIER | c.82-17577G>A | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38648544 | ||||||
| chrX:38648591
|
G | C | 7 | a0001c0001t0001g0075a0001c0001t0001g0077a0001c0001t0001g0084others(4): Show | 7 | HG02559.hp1 HG02615.hp1 HG02647.hp1 others(4): Show |
intron_variant | MODIFIER | c.82-17530G>C | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38648591 | ||||||
| chrX:38648678
|
C | T | 10 | a0001c0001t0001g0023a0001c0001t0002g0022a0001c0001t0002g0065others(7): Show | 10 | HG02257.hp1 HG02630.hp2 HG02809.hp2 others(7): Show |
intron_variant | MODIFIER | c.82-17443C>T | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38648678 | ||||||
| chrX:38648732
|
G | A | 5 | a0001c0001t0002g0102a0001c0001t0002g0127a0001c0001t0002g0149others(2): Show | 5 | HG00099.hp2 HG00642.hp1 HG01515.hp1 others(2): Show |
intron_variant | MODIFIER | c.82-17389G>A | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38648732 | ||||||
| chrX:38648917
|
C | CA | 11 | a0001c0001t0001g0008a0001c0001t0001g0026a0001c0001t0001g0043others(8): Show | 11 | HG00280.hp1 HG02109.hp1 HG02145.hp1 others(8): Show |
intron_variant | MODIFIER | c.82-17187dupA | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 38648917 | |||||
| chrX:38648917
|
CA | C | 1 | a0001c0001t0001g0064 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.82-17187delA | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 38648917 | |||||
| chrX:38648977
|
G | A | 3 | a0001c0001t0001g0089a0001c0001t0005g0078a0001c0002t0001g0074 | 3 | HG02615.hp2 HG02717.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.82-17144G>A | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38648977 | ||||||
| chrX:38648981
|
G | T | 1 | a0001c0001t0001g0180 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.82-17140G>T | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38648981 | ||||||
| chrX:38648983
|
C | T | 4 | a0001c0001t0001g0007a0001c0001t0001g0193a0001c0001t0001g0194others(1): Show | 5 | HG00609.hp1 NA18965.hp1 NA18966.hp1 others(2): Show |
intron_variant | MODIFIER | c.82-17138C>T | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38648983 | ||||||
| chrX:38649067
|
C | A | 1 | a0001c0001t0001g0050 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.82-17054C>A | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38649067 | ||||||
| chrX:38649151
|
C | CA | 1 | a0001c0001t0002g0019 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.82-16969dupA | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 38649151 | |||||
| chrX:38649207
|
G | A | 1 | a0001c0001t0001g0153 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.82-16914G>A | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38649207 | ||||||
| chrX:38649285
|
G | C | 2 | a0001c0001t0001g0129a0001c0001t0001g0164 | 2 | HG01167.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.82-16836G>C | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38649285 | ||||||
| chrX:38649327
|
T | C | 9 | a0001c0001t0001g0077a0001c0001t0001g0084a0001c0001t0001g0089others(6): Show | 9 | HG02559.hp1 HG02615.hp1 HG02615.hp2 others(6): Show |
intron_variant | MODIFIER | c.82-16794T>C | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38649327 | ||||||
| chrX:38649449
|
T | C | 1 | a0001c0001t0001g0073 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.82-16672T>C | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38649449 | ||||||
| chrX:38649633
|
G | A | 1 | a0001c0002t0001g0074 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.82-16488G>A | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38649633 | ||||||
| chrX:38649926
|
T | C | 8 | a0001c0001t0001g0023a0001c0001t0001g0077a0001c0001t0001g0084others(5): Show | 8 | HG02559.hp1 HG02615.hp1 HG02647.hp1 others(5): Show |
intron_variant | MODIFIER | c.82-16195T>C | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38649926 | ||||||
| chrX:38650160
|
G | A | 1 | a0001c0001t0002g0117 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.82-15961G>A | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38650160 | ||||||
| chrX:38650185
|
C | T | 1 | a0001c0001t0001g0166 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.82-15936C>T | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38650185 | ||||||
| chrX:38650472
|
CTGTGAG | C | 30 | a0001c0001t0001g0014a0001c0001t0001g0029a0001c0001t0001g0038others(27): Show | 30 | HG00621.hp1 HG01106.hp1 HG01175.hp2 others(27): Show |
intron_variant | MODIFIER | c.82-15646_82-15641d others(8): Show |
TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 38650472 | |||||
| chrX:38650488
|
G | C | 3 | a0001c0001t0001g0060a0001c0003t0001g0201a0001c0003t0004g0207 | 3 | HG01884.hp2 HG02109.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.82-15633G>C | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38650488 | ||||||
| chrX:38650570
|
C | A | 1 | a0001c0001t0001g0075 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.82-15551C>A | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38650570 | ||||||
| chrX:38650890
|
G | T | 65 | a0001c0001t0001g0014a0001c0001t0001g0023a0001c0001t0001g0029others(62): Show | 66 | HG00621.hp1 HG01106.hp1 HG01175.hp2 others(63): Show |
intron_variant | MODIFIER | c.82-15231G>T | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38650890 | ||||||
| chrX:38651050
|
C | CAT | 5 | a0001c0001t0001g0077a0001c0001t0001g0084a0001c0001t0001g0210others(2): Show | 5 | HG01261.hp1 HG02615.hp1 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.82-15049_82-15048d others(4): Show |
TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 38651050 | |||||
| chrX:38651050
|
C | CATAT | 1 | a0001c0001t0001g0131 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.82-15051_82-15048d others(6): Show |
TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 38651050 | |||||
| chrX:38651050
|
C | CATATATA others(7): Show |
2 | a0001c0001t0001g0187a0001c0001t0002g0067 | 2 | HG01884.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.82-15061_82-15048d others(16): Show |
TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 38651050 | |||||
| chrX:38651050
|
C | CATATATA others(9): Show |
4 | a0001c0001t0002g0022a0001c0001t0002g0069a0001c0001t0002g0076others(1): Show | 4 | HG02630.hp2 HG02809.hp2 HG02896.hp1 others(1): Show |
intron_variant | MODIFIER | c.82-15063_82-15048d others(18): Show |
TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 38651050 | |||||
| chrX:38651050
|
C | CATATATA others(11): Show |
1 | a0001c0001t0001g0075 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.82-15065_82-15048d others(20): Show |
TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 38651050 | |||||
| chrX:38651050
|
C | CATATATA others(15): Show |
2 | a0001c0001t0002g0065a0001c0001t0003g0057 | 2 | HG02257.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.82-15069_82-15048d others(24): Show |
TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 38651050 | |||||
| chrX:38651050
|
C | CATATATA others(19): Show |
1 | a0001c0001t0003g0058 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.82-15048_82-15047i others(28): Show |
TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 38651050 | |||||
| chrX:38651050
|
CAT | C | 106 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(103): Show | 110 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(107): Show |
intron_variant | MODIFIER | c.82-15049_82-15048d others(4): Show |
TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 38651050 | |||||
| chrX:38651050
|
CATAT | C | 46 | a0001c0001t0001g0014a0001c0001t0001g0029a0001c0001t0001g0038others(43): Show | 47 | HG00621.hp1 HG01106.hp1 HG01175.hp2 others(44): Show |
intron_variant | MODIFIER | c.82-15051_82-15048d others(6): Show |
TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 38651050 | |||||
| chrX:38651058
|
T | G | 10 | a0001c0001t0001g0056a0001c0001t0001g0060a0001c0001t0001g0087others(7): Show | 11 | HG01884.hp2 HG02109.hp2 HG02559.hp2 others(8): Show |
intron_variant | MODIFIER | c.82-15063T>G | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38651058 | ||||||
| chrX:38651092
|
A | AG | 1 | a0001c0001t0002g0019 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.82-15026dupG | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 38651092 | |||||
| chrX:38651204
|
G | A | 18 | a0001c0001t0001g0003a0001c0001t0001g0008a0001c0001t0001g0035others(15): Show | 19 | HG00280.hp1 HG00438.hp2 HG00741.hp1 others(16): Show |
intron_variant | MODIFIER | c.82-14917G>A | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38651204 | ||||||
| chrX:38651582
|
G | C | 110 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(107): Show | 114 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(111): Show |
intron_variant | MODIFIER | c.82-14539G>C | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38651582 | ||||||
| chrX:38651600
|
G | C | 1 | a0001c0001t0001g0025 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.82-14521G>C | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38651600 | ||||||
| chrX:38651686
|
G | A | 9 | a0001c0001t0001g0187a0001c0001t0002g0022a0001c0001t0002g0065others(6): Show | 9 | HG01884.hp1 HG02257.hp1 HG02630.hp2 others(6): Show |
intron_variant | MODIFIER | c.82-14435G>A | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38651686 | ||||||
| chrX:38651829
|
A | G | 5 | a0001c0001t0001g0077a0001c0001t0001g0084a0001c0001t0001g0199others(2): Show | 5 | HG02559.hp1 HG02615.hp1 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.82-14292A>G | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38651829 | ||||||
| chrX:38652131
|
C | T | 1 | a0001c0001t0001g0093 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.82-13990C>T | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38652131 | ||||||
| chrX:38652241
|
T | C | 7 | a0001c0001t0001g0083a0001c0001t0001g0089a0001c0001t0001g0091others(4): Show | 7 | HG01891.hp2 HG02615.hp2 HG03130.hp1 others(4): Show |
intron_variant | MODIFIER | c.82-13880T>C | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38652241 | ||||||
| chrX:38652777
|
C | T | 109 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(106): Show | 113 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(110): Show |
intron_variant | MODIFIER | c.82-13344C>T | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38652777 | ||||||
| chrX:38652874
|
C | T | 1 | a0001c0003t0004g0207 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.82-13247C>T | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38652874 | ||||||
| chrX:38652880
|
A | T | 1 | a0001c0001t0001g0159 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.82-13241A>T | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38652880 | ||||||
| chrX:38653012
|
C | T | 40 | a0001c0001t0001g0014a0001c0001t0001g0029a0001c0001t0001g0038others(37): Show | 41 | HG00621.hp1 HG01106.hp1 HG01175.hp2 others(38): Show |
intron_variant | MODIFIER | c.82-13109C>T | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38653012 | ||||||
| chrX:38653053
|
C | T | 2 | a0001c0001t0002g0080a0001c0003t0001g0200 | 2 | HG03471.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.82-13068C>T | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38653053 | ||||||
| chrX:38653118
|
G | A | 1 | a0001c0001t0002g0165 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.82-13003G>A | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38653118 | ||||||
| chrX:38653192
|
C | T | 1 | a0001c0001t0001g0169 | 1 | NA18991.hp2 | intron_variant | MODIFIER | c.82-12929C>T | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38653192 | ||||||
| chrX:38653193
|
G | A | 27 | a0001c0001t0001g0014a0001c0001t0001g0029a0001c0001t0001g0038others(24): Show | 27 | HG00621.hp1 HG01106.hp1 HG01175.hp2 others(24): Show |
intron_variant | MODIFIER | c.82-12928G>A | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38653193 | ||||||
| chrX:38653328
|
G | A | 1 | a0001c0001t0001g0056 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.82-12793G>A | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38653328 | ||||||
| chrX:38653359
|
A | G | 40 | a0001c0001t0001g0014a0001c0001t0001g0029a0001c0001t0001g0038others(37): Show | 41 | HG00621.hp1 HG01106.hp1 HG01175.hp2 others(38): Show |
intron_variant | MODIFIER | c.82-12762A>G | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38653359 | ||||||
| chrX:38654194
|
G | A | 29 | a0001c0001t0001g0014a0001c0001t0001g0029a0001c0001t0001g0038others(26): Show | 29 | HG00621.hp1 HG01106.hp1 HG01175.hp2 others(26): Show |
intron_variant | MODIFIER | c.82-11927G>A | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38654194 | ||||||
| chrX:38654257
|
G | C | 2 | a0001c0001t0002g0080a0001c0003t0001g0200 | 2 | HG03471.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.82-11864G>C | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38654257 | ||||||
| chrX:38654720
|
CATGAATA others(2): Show |
C | 175 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(172): Show | 180 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(177): Show |
intron_variant | MODIFIER | c.82-11390_82-11382d others(11): Show |
TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 38654720 | |||||
| chrX:38654819
|
G | GA | 1 | a0001c0001t0002g0161 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.82-11301dupA | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 38654819 | |||||
| chrX:38654975
|
T | G | 1 | a0001c0002t0001g0088 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.82-11146T>G | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38654975 | ||||||
| chrX:38655206
|
G | A | 1 | a0001c0001t0002g0161 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.82-10915G>A | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38655206 | ||||||
| chrX:38655223
|
AG | A | 1 | a0001c0001t0002g0161 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.82-10894delG | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 38655223 | |||||
| chrX:38655308
|
A | AG | 1 | a0001c0001t0002g0161 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.82-10807dupG | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 38655308 | |||||
| chrX:38655490
|
G | GT | 8 | a0001c0001t0002g0102a0001c0001t0002g0124a0001c0001t0002g0127others(5): Show | 8 | HG00099.hp2 HG00642.hp1 HG01515.hp1 others(5): Show |
intron_variant | MODIFIER | c.82-10621dupT | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 38655490 | |||||
| chrX:38655671
|
C | A | 7 | a0001c0001t0001g0023a0001c0001t0001g0059a0001c0001t0001g0071others(4): Show | 7 | HG02055.hp1 HG02572.hp1 HG02895.hp1 others(4): Show |
intron_variant | MODIFIER | c.82-10450C>A | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38655671 | ||||||
| chrX:38655695
|
G | A | 158 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(155): Show | 163 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(160): Show |
intron_variant | MODIFIER | c.82-10426G>A | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38655695 | ||||||
| chrX:38655714
|
AC | A | 1 | a0001c0001t0002g0161 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.82-10403delC | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 38655714 | |||||
| chrX:38655909
|
CA | C | 1 | a0001c0001t0002g0161 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.82-10209delA | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 38655909 | |||||
| chrX:38655915
|
G | T | 175 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(172): Show | 181 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(178): Show |
intron_variant | MODIFIER | c.82-10206G>T | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38655915 | ||||||
| chrX:38655942
|
G | T | 1 | a0001c0001t0002g0161 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.82-10179G>T | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38655942 | ||||||
| chrX:38655944
|
G | GTATTGC | 1 | a0001c0001t0002g0161 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.82-10177_82-10176i others(8): Show |
TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38655944 | ||||||
| chrX:38655966
|
TG | T | 1 | a0001c0001t0002g0161 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.82-10153delG | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 38655966 | |||||
| chrX:38655986
|
G | GT | 1 | a0001c0001t0002g0161 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.82-10130dupT | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 38655986 | |||||
| chrX:38655995
|
GA | G | 1 | a0001c0001t0002g0161 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.82-10125delA | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38655995 | ||||||
| chrX:38656115
|
A | AG | 1 | a0001c0001t0002g0161 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.82-10004dupG | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 38656115 | |||||
| chrX:38656162
|
G | A | 1 | a0001c0001t0002g0031 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.82-9959G>A | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38656162 | ||||||
| chrX:38656279
|
A | G | 4 | a0001c0002t0001g0074a0001c0002t0001g0212a0001c0002t0001g0213others(1): Show | 4 | HG02257.hp2 HG02717.hp1 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.82-9842A>G | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38656279 | ||||||
| chrX:38656329
|
C | CT | 1 | a0001c0001t0002g0161 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.82-9790dupT | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 38656329 | |||||
| chrX:38656781
|
T | G | 4 | a0001c0001t0001g0061a0001c0001t0001g0062a0001c0001t0001g0063others(1): Show | 4 | HG02723.hp2 HG02809.hp1 HG02896.hp2 others(1): Show |
intron_variant | MODIFIER | c.82-9340T>G | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38656781 | ||||||
| chrX:38657202
|
G | C | 36 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0010others(33): Show | 38 | HG00099.hp1 HG01069.hp1 HG01071.hp2 others(35): Show |
intron_variant | MODIFIER | c.82-8919G>C | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38657202 | ||||||
| chrX:38657697
|
T | A | 18 | a0001c0001t0001g0056a0001c0001t0001g0060a0001c0001t0001g0087others(15): Show | 19 | HG01884.hp1 HG02145.hp1 HG02257.hp1 others(16): Show |
intron_variant | MODIFIER | c.82-8424T>A | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38657697 | ||||||
| chrX:38657705
|
G | A | 2 | a0001c0003t0001g0181a0001c0003t0001g0215 | 2 | HG02258.hp1 HG02622.hp1 |
intron_variant | MODIFIER | c.82-8416G>A | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38657705 | ||||||
| chrX:38658040
|
C | A | 1 | a0001c0001t0001g0128 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.82-8081C>A | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38658040 | ||||||
| chrX:38658115
|
T | TAA | 168 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(165): Show | 175 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(172): Show |
intron_variant | MODIFIER | c.82-8004_82-8003dup others(2): Show |
TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 38658115 | |||||
| chrX:38658347
|
A | AT | 8 | a0001c0001t0001g0049a0001c0001t0002g0022a0001c0001t0002g0065others(5): Show | 8 | HG01884.hp2 HG02257.hp1 HG02809.hp2 others(5): Show |
intron_variant | MODIFIER | c.82-7759dupT | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 38658347 | |||||
| chrX:38658347
|
AT | A | 18 | a0001c0001t0001g0056a0001c0001t0001g0060a0001c0001t0001g0087others(15): Show | 19 | HG01884.hp1 HG02145.hp1 HG02257.hp2 others(16): Show |
intron_variant | MODIFIER | c.82-7759delT | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 38658347 | |||||
| chrX:38658426
|
C | T | 3 | a0001c0001t0001g0083a0001c0001t0002g0081a0001c0003t0001g0200 | 3 | HG01891.hp2 HG03209.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.82-7695C>T | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38658426 | ||||||
| chrX:38659001
|
T | TAC | 4 | a0001c0001t0001g0203a0001c0001t0001g0206a0001c0001t0002g0208others(1): Show | 4 | HG02615.hp2 HG02630.hp1 HG02818.hp2 others(1): Show |
intron_variant | MODIFIER | c.82-7083_82-7082dup others(2): Show |
TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 38659001 | |||||
| chrX:38659001
|
TAC | T | 23 | a0001c0001t0001g0007a0001c0001t0001g0025a0001c0001t0001g0060others(20): Show | 25 | HG00609.hp1 HG01099.hp1 HG01255.hp1 others(22): Show |
intron_variant | MODIFIER | c.82-7083_82-7082del others(2): Show |
TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 38659001 | |||||
| chrX:38659001
|
TACAC | T | 128 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(125): Show | 131 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(128): Show |
intron_variant | MODIFIER | c.82-7085_82-7082del others(4): Show |
TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 38659001 | |||||
| chrX:38659001
|
TACACAC | T | 11 | a0001c0001t0001g0009a0001c0001t0001g0077a0001c0001t0001g0083others(8): Show | 11 | HG01891.hp2 HG01975.hp1 HG02257.hp2 others(8): Show |
intron_variant | MODIFIER | c.82-7087_82-7082del others(6): Show |
TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 38659001 | |||||
| chrX:38659001
|
TACACACA others(1): Show |
T | 1 | a0001c0001t0001g0146 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.82-7089_82-7082del others(8): Show |
TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 38659001 | |||||
| chrX:38659001
|
TACACACA others(3): Show |
T | 2 | a0001c0002t0001g0212a0001c0002t0001g0213 | 2 | HG03195.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.82-7091_82-7082del others(10): Show |
TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 38659001 | |||||
| chrX:38659001
|
TACACACA others(7): Show |
T | 36 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0010others(33): Show | 38 | HG00099.hp1 HG01069.hp1 HG01071.hp2 others(35): Show |
intron_variant | MODIFIER | c.82-7095_82-7082del others(14): Show |
TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 38659001 | |||||
| chrX:38659038
|
A | C | 1 | a0001c0003t0001g0200 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.82-7083A>C | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38659038 | ||||||
| chrX:38659038
|
ACC | A | 1 | a0001c0001t0001g0082 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.82-7081_82-7080del others(2): Show |
TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 38659038 | |||||
| chrX:38659069
|
C | CAA | 168 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(165): Show | 175 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(172): Show |
intron_variant | MODIFIER | c.82-7052_82-7051ins others(2): Show |
TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38659069 | ||||||
| chrX:38659280
|
C | T | 1 | a0001c0001t0001g0144 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.82-6841C>T | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38659280 | ||||||
| chrX:38659657
|
A | T | 36 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0010others(33): Show | 38 | HG00099.hp1 HG01069.hp1 HG01071.hp2 others(35): Show |
intron_variant | MODIFIER | c.82-6464A>T | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38659657 | ||||||
| chrX:38659664
|
A | AT | 52 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0010others(49): Show | 55 | HG00099.hp1 HG01069.hp1 HG01071.hp2 others(52): Show |
intron_variant | MODIFIER | c.82-6442dupT | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 38659664 | |||||
| chrX:38659664
|
A | ATT | 6 | a0001c0001t0001g0120a0001c0001t0001g0132a0001c0001t0001g0141others(3): Show | 6 | HG01109.hp1 HG04228.hp1 NA18942.hp1 others(3): Show |
intron_variant | MODIFIER | c.82-6443_82-6442dup others(2): Show |
TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 38659664 | |||||
| chrX:38659664
|
A | ATTT | 88 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(85): Show | 92 | HG00140.hp1 HG00280.hp1 HG00438.hp2 others(89): Show |
intron_variant | MODIFIER | c.82-6444_82-6442dup others(3): Show |
TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 38659664 | |||||
| chrX:38659664
|
AT | A | 1 | a0001c0002t0001g0212 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.82-6442delT | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 38659664 | |||||
| chrX:38659724
|
T | G | 2 | a0001c0001t0002g0081a0001c0003t0001g0200 | 2 | HG03209.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.82-6397T>G | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38659724 | ||||||
| chrX:38659773
|
A | T | 12 | a0001c0001t0001g0023a0001c0001t0001g0059a0001c0001t0001g0071others(9): Show | 13 | HG02055.hp1 HG02559.hp2 HG02572.hp1 others(10): Show |
intron_variant | MODIFIER | c.82-6348A>T | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38659773 | ||||||
| chrX:38659817
|
CTTTTTCT others(2): Show |
C | 1 | a0001c0003t0001g0200 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.82-6298_82-6290del others(9): Show |
TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 38659817 | |||||
| chrX:38659823
|
C | CT | 2 | a0001c0001t0002g0032a0001c0001t0002g0161 | 2 | HG03831.hp1 NA19067.hp1 |
intron_variant | MODIFIER | c.82-6277dupT | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 38659823 | |||||
| chrX:38659823
|
C | CTT | 1 | a0001c0001t0002g0102 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.82-6278_82-6277dup others(2): Show |
TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 38659823 | |||||
| chrX:38659823
|
CT | C | 13 | a0001c0001t0001g0056a0001c0001t0001g0060a0001c0001t0001g0077others(10): Show | 13 | HG01891.hp2 HG02145.hp1 HG02602.hp1 others(10): Show |
intron_variant | MODIFIER | c.82-6277delT | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 38659823 | |||||
| chrX:38659823
|
CTT | C | 42 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(39): Show | 45 | HG00099.hp1 HG01069.hp1 HG01071.hp2 others(42): Show |
intron_variant | MODIFIER | c.82-6278_82-6277del others(2): Show |
TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 38659823 | |||||
| chrX:38659823
|
CTTT | C | 101 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0007others(98): Show | 104 | HG00140.hp1 HG00280.hp1 HG00438.hp2 others(101): Show |
intron_variant | MODIFIER | c.82-6279_82-6277del others(3): Show |
TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 38659823 | |||||
| chrX:38659823
|
CTTTT | C | 13 | a0001c0001t0001g0023a0001c0001t0001g0043a0001c0001t0001g0059others(10): Show | 14 | HG02559.hp2 HG02572.hp1 HG02818.hp1 others(11): Show |
intron_variant | MODIFIER | c.82-6280_82-6277del others(4): Show |
TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 38659823 | |||||
| chrX:38659861
|
C | G | 1 | a0001c0001t0001g0134 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.82-6260C>G | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38659861 | ||||||
| chrX:38659880
|
A | G | 2 | a0001c0003t0001g0066a0001c0003t0001g0201 | 2 | HG01884.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.82-6241A>G | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38659880 | ||||||
| chrX:38659987
|
C | T | 1 | a0001c0001t0001g0171 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.82-6134C>T | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38659987 | ||||||
| chrX:38660025
|
C | T | 1 | a0001c0001t0001g0134 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.82-6096C>T | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38660025 | ||||||
| chrX:38660130
|
GC | G | 1 | a0001c0001t0002g0161 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.82-5987delC | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 38660130 | |||||
| chrX:38660422
|
C | T | 1 | a0001c0001t0002g0097 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.82-5699C>T | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38660422 | ||||||
| chrX:38660432
|
C | G | 3 | a0001c0003t0001g0066a0001c0003t0001g0201a0001c0003t0004g0207 | 3 | HG01884.hp2 HG02109.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.82-5689C>G | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38660432 | ||||||
| chrX:38660562
|
G | A | 4 | a0001c0001t0001g0027a0001c0001t0001g0041a0001c0001t0001g0104others(1): Show | 4 | NA18962.hp1 NA18963.hp1 NA18974.hp1 others(1): Show |
intron_variant | MODIFIER | c.82-5559G>A | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38660562 | ||||||
| chrX:38660562
|
G | T | 6 | a0001c0001t0002g0022a0001c0001t0002g0065a0001c0001t0002g0067others(3): Show | 6 | HG02257.hp1 HG02809.hp2 HG02818.hp2 others(3): Show |
intron_variant | MODIFIER | c.82-5559G>T | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38660562 | ||||||
| chrX:38660584
|
A | T | 1 | a0001c0001t0001g0202 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.82-5537A>T | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38660584 | ||||||
| chrX:38660766
|
A | G | 36 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0010others(33): Show | 38 | HG00099.hp1 HG01069.hp1 HG01071.hp2 others(35): Show |
intron_variant | MODIFIER | c.82-5355A>G | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38660766 | ||||||
| chrX:38660849
|
T | C | 5 | a0001c0001t0002g0022a0001c0001t0002g0065a0001c0001t0002g0067others(2): Show | 5 | HG02257.hp1 HG02809.hp2 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.82-5272T>C | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38660849 | ||||||
| chrX:38661376
|
A | G | 1 | a0001c0001t0001g0185 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.82-4745A>G | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38661376 | ||||||
| chrX:38661676
|
G | A | 174 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(171): Show | 181 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(178): Show |
intron_variant | MODIFIER | c.82-4445G>A | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38661676 | ||||||
| chrX:38661770
|
C | T | 1 | a0001c0001t0001g0194 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.82-4351C>T | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38661770 | ||||||
| chrX:38661834
|
T | TA | 52 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0010others(49): Show | 54 | HG00099.hp1 HG01069.hp1 HG01071.hp2 others(51): Show |
intron_variant | MODIFIER | c.82-4277dupA | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 38661834 | |||||
| chrX:38661834
|
TA | T | 1 | a0001c0001t0001g0104 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.82-4277delA | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 38661834 | |||||
| chrX:38661954
|
T | A | 2 | a0001c0002t0001g0212a0001c0002t0001g0213 | 2 | HG03195.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.82-4167T>A | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38661954 | ||||||
| chrX:38661958
|
T | C | 13 | a0001c0001t0001g0023a0001c0001t0001g0059a0001c0001t0001g0071others(10): Show | 14 | HG02055.hp1 HG02559.hp2 HG02572.hp1 others(11): Show |
intron_variant | MODIFIER | c.82-4163T>C | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38661958 | ||||||
| chrX:38662000
|
G | T | 4 | a0001c0002t0001g0074a0001c0002t0001g0212a0001c0002t0001g0213others(1): Show | 4 | HG02257.hp2 HG02717.hp1 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.82-4121G>T | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38662000 | ||||||
| chrX:38662060
|
G | A | 1 | a0001c0001t0002g0208 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.82-4061G>A | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38662060 | ||||||
| chrX:38662335
|
G | A | 1 | a0001c0001t0001g0091 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.82-3786G>A | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38662335 | ||||||
| chrX:38662445
|
G | C | 3 | a0001c0001t0003g0057a0001c0001t0003g0058a0001c0001t0003g0079 | 3 | HG02630.hp2 HG02976.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.82-3676G>C | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38662445 | ||||||
| chrX:38662483
|
G | T | 1 | a0001c0001t0002g0069 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.82-3638G>T | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38662483 | ||||||
| chrX:38662542
|
G | A | 2 | a0001c0001t0001g0111a0001c0001t0001g0112 | 2 | HG03491.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.82-3579G>A | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38662542 | ||||||
| chrX:38662602
|
G | A | 1 | a0001c0002t0001g0213 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.82-3519G>A | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38662602 | ||||||
| chrX:38662609
|
AG | A | 106 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(103): Show | 111 | HG00140.hp1 HG00280.hp1 HG00438.hp2 others(108): Show |
intron_variant | MODIFIER | c.82-3510delG | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 38662609 | |||||
| chrX:38662806
|
G | T | 4 | a0001c0002t0001g0074a0001c0002t0001g0212a0001c0002t0001g0213others(1): Show | 4 | HG02257.hp2 HG02717.hp1 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.82-3315G>T | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38662806 | ||||||
| chrX:38662953
|
T | C | 43 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0010others(40): Show | 45 | HG00099.hp1 HG01069.hp1 HG01071.hp2 others(42): Show |
intron_variant | MODIFIER | c.82-3168T>C | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38662953 | ||||||
| chrX:38662982
|
C | T | 7 | a0001c0001t0001g0056a0001c0001t0001g0060a0001c0001t0001g0083others(4): Show | 7 | HG01884.hp1 HG01891.hp2 HG02145.hp1 others(4): Show |
intron_variant | MODIFIER | c.82-3139C>T | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38662982 | ||||||
| chrX:38663081
|
C | T | 1 | a0001c0001t0001g0166 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.82-3040C>T | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38663081 | ||||||
| chrX:38663152
|
TAC | T | 149 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(146): Show | 154 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(151): Show |
intron_variant | MODIFIER | c.82-2941_82-2940del others(2): Show |
TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 38663152 | |||||
| chrX:38663152
|
TACAC | T | 43 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0010others(40): Show | 45 | HG00099.hp1 HG00438.hp2 HG01069.hp1 others(42): Show |
intron_variant | MODIFIER | c.82-2943_82-2940del others(4): Show |
TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 38663152 | |||||
| chrX:38663178
|
C | G | 16 | a0001c0001t0001g0056a0001c0001t0001g0060a0001c0001t0001g0077others(13): Show | 16 | HG01884.hp1 HG01891.hp2 HG02145.hp1 others(13): Show |
intron_variant | MODIFIER | c.82-2943C>G | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38663178 | ||||||
| chrX:38663178
|
CACAG | C | 1 | a0001c0001t0001g0075 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.82-2939_82-2936del others(4): Show |
TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 38663178 | |||||
| chrX:38663180
|
CAG | C | 16 | a0001c0001t0001g0056a0001c0001t0001g0060a0001c0001t0001g0077others(13): Show | 16 | HG01884.hp1 HG01891.hp2 HG02145.hp1 others(13): Show |
intron_variant | MODIFIER | c.82-2939_82-2938del others(2): Show |
TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 38663180 | |||||
| chrX:38663184
|
C | G | 1 | a0001c0001t0001g0075 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.82-2937C>G | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38663184 | ||||||
| chrX:38663203
|
T | C | 1 | a0001c0001t0002g0020 | 1 | NA19055.hp1 | intron_variant | MODIFIER | c.82-2918T>C | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38663203 | ||||||
| chrX:38663254
|
C | G | 16 | a0001c0001t0001g0056a0001c0001t0001g0060a0001c0001t0001g0077others(13): Show | 16 | HG01884.hp1 HG01891.hp2 HG02145.hp1 others(13): Show |
intron_variant | MODIFIER | c.82-2867C>G | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38663254 | ||||||
| chrX:38663369
|
G | C | 1 | a0001c0001t0001g0082 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.82-2752G>C | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38663369 | ||||||
| chrX:38663410
|
G | A | 1 | a0001c0001t0002g0031 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.82-2711G>A | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38663410 | ||||||
| chrX:38663443
|
G | A | 12 | a0001c0001t0001g0056a0001c0001t0001g0060a0001c0001t0001g0077others(9): Show | 12 | HG01884.hp1 HG01891.hp2 HG02145.hp1 others(9): Show |
intron_variant | MODIFIER | c.82-2678G>A | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38663443 | ||||||
| chrX:38663626
|
G | C | 4 | a0001c0001t0001g0007a0001c0001t0001g0193a0001c0001t0001g0194others(1): Show | 5 | HG00609.hp1 NA18965.hp1 NA18966.hp1 others(2): Show |
intron_variant | MODIFIER | c.82-2495G>C | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38663626 | ||||||
| chrX:38663668
|
T | G | 1 | a0002c0004t0001g0173 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.82-2453T>G | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38663668 | ||||||
| chrX:38663858
|
G | C | 6 | a0001c0003t0001g0066a0001c0003t0001g0181a0001c0003t0001g0200others(3): Show | 6 | HG01884.hp2 HG02109.hp2 HG02258.hp1 others(3): Show |
intron_variant | MODIFIER | c.82-2263G>C | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38663858 | ||||||
| chrX:38664018
|
C | T | 12 | a0001c0001t0001g0056a0001c0001t0001g0060a0001c0001t0001g0077others(9): Show | 12 | HG01884.hp1 HG01891.hp2 HG02145.hp1 others(9): Show |
intron_variant | MODIFIER | c.82-2103C>T | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38664018 | ||||||
| chrX:38664085
|
G | T | 6 | a0001c0003t0001g0066a0001c0003t0001g0181a0001c0003t0001g0200others(3): Show | 6 | HG01884.hp2 HG02109.hp2 HG02258.hp1 others(3): Show |
intron_variant | MODIFIER | c.82-2036G>T | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38664085 | ||||||
| chrX:38664443
|
G | T | 1 | a0001c0003t0004g0207 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.82-1678G>T | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38664443 | ||||||
| chrX:38664621
|
T | C | 1 | a0001c0001t0001g0053 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.82-1500T>C | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38664621 | ||||||
| chrX:38664832
|
G | A | 1 | a0001c0001t0001g0204 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.82-1289G>A | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38664832 | ||||||
| chrX:38664876
|
C | T | 93 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(90): Show | 97 | HG00140.hp1 HG00280.hp1 HG00438.hp2 others(94): Show |
intron_variant | MODIFIER | c.82-1245C>T | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38664876 | ||||||
| chrX:38664932
|
G | A | 16 | a0001c0001t0001g0056a0001c0001t0001g0060a0001c0001t0001g0077others(13): Show | 16 | HG01884.hp1 HG01891.hp2 HG02145.hp1 others(13): Show |
intron_variant | MODIFIER | c.82-1189G>A | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38664932 | ||||||
| chrX:38664999
|
G | A | 4 | a0001c0002t0001g0074a0001c0002t0001g0212a0001c0002t0001g0213others(1): Show | 4 | HG02257.hp2 HG02717.hp1 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.82-1122G>A | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38664999 | ||||||
| chrX:38665162
|
C | T | 1 | a0001c0001t0001g0187 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.82-959C>T | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38665162 | ||||||
| chrX:38665398
|
G | T | 1 | a0001c0001t0001g0139 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.82-723G>T | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38665398 | ||||||
| chrX:38665597
|
A | G | 174 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(171): Show | 181 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(178): Show |
intron_variant | MODIFIER | c.82-524A>G | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38665597 | ||||||
| chrX:38665719
|
T | C | 1 | a0001c0001t0001g0169 | 1 | NA18991.hp2 | intron_variant | MODIFIER | c.82-402T>C | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38665719 | ||||||
| chrX:38665742
|
AG | A | 1 | a0001c0001t0005g0078 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.82-376delG | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 38665742 | |||||
| chrX:38665989
|
G | A | 1 | a0001c0001t0002g0076 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.82-132G>A | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 1/7 | chrX | 38665989 | ||||||
| chrX:38666371
|
A | G | 1 | a0001c0001t0005g0078 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.270+62A>G | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 2/7 | chrX | 38666371 | ||||||
| chrX:38666371
|
A | T | 12 | a0001c0001t0001g0056a0001c0001t0001g0060a0001c0001t0001g0077others(9): Show | 12 | HG01884.hp1 HG01891.hp2 HG02145.hp1 others(9): Show |
intron_variant | MODIFIER | c.270+62A>T | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 2/7 | chrX | 38666371 | ||||||
| chrX:38666597
|
CT | C | 164 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(161): Show | 171 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(168): Show |
intron_variant | MODIFIER | c.270+302delT | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chrX | 38666597 | |||||
| chrX:38666597
|
CTT | C | 9 | a0001c0001t0001g0160a0001c0001t0001g0205a0001c0001t0002g0081others(6): Show | 9 | HG01884.hp2 HG02109.hp2 HG02145.hp1 others(6): Show |
intron_variant | MODIFIER | c.270+301_270+302del others(2): Show |
TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chrX | 38666597 | |||||
| chrX:38666791
|
G | A | 1 | a0001c0001t0001g0063 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.270+482G>A | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 2/7 | chrX | 38666791 | ||||||
| chrX:38666797
|
T | A | 1 | a0001c0001t0001g0108 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.270+488T>A | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 2/7 | chrX | 38666797 | ||||||
| chrX:38666807
|
G | A | 93 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(90): Show | 97 | HG00140.hp1 HG00280.hp1 HG00438.hp2 others(94): Show |
intron_variant | MODIFIER | c.270+498G>A | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 2/7 | chrX | 38666807 | ||||||
| chrX:38667161
|
T | C | 168 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(165): Show | 175 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(172): Show |
intron_variant | MODIFIER | c.270+852T>C | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 2/7 | chrX | 38667161 | ||||||
| chrX:38667283
|
C | G | 12 | a0001c0001t0001g0056a0001c0001t0001g0060a0001c0001t0001g0077others(9): Show | 12 | HG01884.hp1 HG01891.hp2 HG02145.hp1 others(9): Show |
intron_variant | MODIFIER | c.270+974C>G | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 2/7 | chrX | 38667283 | ||||||
| chrX:38667366
|
G | A | 8 | a0001c0002t0001g0001a0001c0002t0001g0068a0001c0002t0001g0074others(5): Show | 9 | HG02257.hp2 HG02559.hp2 HG02717.hp1 others(6): Show |
intron_variant | MODIFIER | c.270+1057G>A | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 2/7 | chrX | 38667366 | ||||||
| chrX:38667505
|
A | G | 3 | a0001c0001t0003g0057a0001c0001t0003g0058a0001c0001t0003g0079 | 3 | HG02630.hp2 HG02976.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.270+1196A>G | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 2/7 | chrX | 38667505 | ||||||
| chrX:38667506
|
C | A | 1 | a0001c0001t0001g0029 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.270+1197C>A | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 2/7 | chrX | 38667506 | ||||||
| chrX:38667595
|
A | G | 36 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0010others(33): Show | 38 | HG00099.hp1 HG01069.hp1 HG01071.hp2 others(35): Show |
intron_variant | MODIFIER | c.270+1286A>G | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 2/7 | chrX | 38667595 | ||||||
| chrX:38668119
|
T | C | 1 | a0001c0001t0001g0148 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.270+1810T>C | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 2/7 | chrX | 38668119 | ||||||
| chrX:38668168
|
T | G | 8 | a0001c0001t0001g0023a0001c0001t0001g0059a0001c0001t0001g0071others(5): Show | 8 | HG02055.hp1 HG02572.hp1 HG02895.hp1 others(5): Show |
intron_variant | MODIFIER | c.270+1859T>G | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 2/7 | chrX | 38668168 | ||||||
| chrX:38668173
|
C | G | 1 | a0001c0001t0001g0096 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.270+1864C>G | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 2/7 | chrX | 38668173 | ||||||
| chrX:38668513
|
G | C | 3 | a0001c0003t0001g0066a0001c0003t0001g0201a0001c0003t0004g0207 | 3 | HG01884.hp2 HG02109.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.270+2204G>C | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 2/7 | chrX | 38668513 | ||||||
| chrX:38668935
|
T | A | 1 | a0001c0001t0001g0171 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.271-2441T>A | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 2/7 | chrX | 38668935 | ||||||
| chrX:38668936
|
A | AT | 91 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(88): Show | 95 | HG00140.hp1 HG00280.hp1 HG00438.hp2 others(92): Show |
intron_variant | MODIFIER | c.271-2429dupT | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chrX | 38668936 | |||||
| chrX:38668936
|
A | ATT | 1 | a0001c0001t0001g0158 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.271-2430_271-2429d others(4): Show |
TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chrX | 38668936 | |||||
| chrX:38668936
|
AT | A | 26 | a0001c0001t0001g0056a0001c0001t0001g0060a0001c0001t0001g0077others(23): Show | 27 | HG01884.hp1 HG01884.hp2 HG01891.hp2 others(24): Show |
intron_variant | MODIFIER | c.271-2429delT | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chrX | 38668936 | |||||
| chrX:38669637
|
G | A | 6 | a0001c0003t0001g0066a0001c0003t0001g0181a0001c0003t0001g0200others(3): Show | 6 | HG01884.hp2 HG02109.hp2 HG02258.hp1 others(3): Show |
intron_variant | MODIFIER | c.271-1739G>A | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 2/7 | chrX | 38669637 | ||||||
| chrX:38670219
|
A | G | 1 | a0001c0001t0001g0009 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.271-1157A>G | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 2/7 | chrX | 38670219 | ||||||
| chrX:38670254
|
A | G | 7 | a0001c0001t0001g0023a0001c0001t0001g0059a0001c0001t0001g0071others(4): Show | 7 | HG02055.hp1 HG02572.hp1 HG02895.hp1 others(4): Show |
intron_variant | MODIFIER | c.271-1122A>G | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 2/7 | chrX | 38670254 | ||||||
| chrX:38670286
|
G | A | 1 | a0001c0001t0001g0023 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.271-1090G>A | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 2/7 | chrX | 38670286 | ||||||
| chrX:38670374
|
C | G | 48 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0010others(45): Show | 50 | HG00099.hp1 HG01069.hp1 HG01071.hp2 others(47): Show |
intron_variant | MODIFIER | c.271-1002C>G | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 2/7 | chrX | 38670374 | ||||||
| chrX:38670495
|
A | G | 6 | a0001c0003t0001g0066a0001c0003t0001g0181a0001c0003t0001g0200others(3): Show | 6 | HG01884.hp2 HG02109.hp2 HG02258.hp1 others(3): Show |
intron_variant | MODIFIER | c.271-881A>G | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 2/7 | chrX | 38670495 | ||||||
| chrX:38670883
|
G | T | 1 | a0001c0001t0001g0105 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.271-493G>T | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 2/7 | chrX | 38670883 | ||||||
| chrX:38671133
|
G | A | 4 | a0001c0001t0001g0023a0001c0001t0001g0090a0001c0001t0001g0091others(1): Show | 4 | HG02572.hp1 HG03130.hp1 HG03540.hp2 others(1): Show |
intron_variant | MODIFIER | c.271-243G>A | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 2/7 | chrX | 38671133 | ||||||
| chrX:38671791
|
C | T | 9 | a0001c0001t0001g0023a0001c0001t0001g0059a0001c0001t0001g0071others(6): Show | 9 | HG02055.hp1 HG02572.hp1 HG02615.hp2 others(6): Show |
intron_variant | MODIFIER | c.345+341C>T | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 3/7 | chrX | 38671791 | ||||||
| chrX:38671823
|
C | A | 1 | a0001c0001t0001g0089 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.345+373C>A | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 3/7 | chrX | 38671823 | ||||||
| chrX:38671853
|
G | A | 1 | a0001c0003t0001g0215 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.345+403G>A | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 3/7 | chrX | 38671853 | ||||||
| chrX:38671889
|
A | G | 1 | a0001c0001t0001g0045 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.345+439A>G | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 3/7 | chrX | 38671889 | ||||||
| chrX:38671904
|
T | A | 1 | a0001c0001t0001g0045 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.345+454T>A | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 3/7 | chrX | 38671904 | ||||||
| chrX:38672224
|
A | G | 4 | a0001c0001t0001g0010a0001c0001t0001g0011a0001c0001t0001g0116others(1): Show | 4 | HG01069.hp1 HG01071.hp2 HG01074.hp1 others(1): Show |
intron_variant | MODIFIER | c.345+774A>G | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 3/7 | chrX | 38672224 | ||||||
| chrX:38672228
|
GA | G | 1 | a0001c0002t0001g0092 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.345+786delA | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chrX | 38672228 | |||||
| chrX:38672309
|
T | A | 3 | a0001c0001t0001g0084a0001c0001t0001g0210a0001c0001t0001g0211 | 3 | HG02615.hp1 HG02723.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.345+859T>A | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 3/7 | chrX | 38672309 | ||||||
| chrX:38672360
|
C | T | 2 | a0001c0001t0001g0129a0001c0001t0001g0164 | 2 | HG01167.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.345+910C>T | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 3/7 | chrX | 38672360 | ||||||
| chrX:38672619
|
C | T | 1 | a0001c0001t0001g0075 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.345+1169C>T | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 3/7 | chrX | 38672619 | ||||||
| chrX:38673364
|
C | CT | 19 | a0001c0001t0001g0012a0001c0001t0001g0029a0001c0001t0001g0118others(16): Show | 20 | HG01169.hp1 HG01884.hp2 HG01928.hp1 others(17): Show |
intron_variant | MODIFIER | c.346-836dupT | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chrX | 38673364 | |||||
| chrX:38673364
|
C | CTT | 1 | a0001c0001t0001g0170 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.346-837_346-836dup others(2): Show |
TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chrX | 38673364 | |||||
| chrX:38673364
|
CT | C | 18 | a0001c0001t0001g0011a0001c0001t0001g0023a0001c0001t0001g0071others(15): Show | 18 | HG00099.hp2 HG01069.hp1 HG01074.hp1 others(15): Show |
intron_variant | MODIFIER | c.346-836delT | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chrX | 38673364 | |||||
| chrX:38673702
|
C | CT | 1 | a0001c0001t0001g0185 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.346-509dupT | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chrX | 38673702 | |||||
| chrX:38673982
|
A | G | 1 | a0001c0001t0002g0081 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.346-239A>G | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 3/7 | chrX | 38673982 | ||||||
| chrX:38674036
|
G | A | 5 | a0001c0001t0001g0003a0001c0001t0001g0119a0001c0001t0001g0123others(2): Show | 6 | HG01257.hp1 HG01975.hp2 HG01981.hp1 others(3): Show |
intron_variant | MODIFIER | c.346-185G>A | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 3/7 | chrX | 38674036 | ||||||
| chrX:38674782
|
G | C | 1 | a0001c0001t0001g0205 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.441+466G>C | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 4/7 | chrX | 38674782 | ||||||
| chrX:38674959
|
TAAAAG | T | 1 | a0001c0001t0001g0216 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.441+644_441+648del others(5): Show |
TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 4/7 | chrX | 38674959 | ||||||
| chrX:38675046
|
G | A | 12 | a0001c0001t0001g0056a0001c0001t0001g0060a0001c0001t0001g0077others(9): Show | 12 | HG01884.hp1 HG01891.hp2 HG02145.hp1 others(9): Show |
intron_variant | MODIFIER | c.442-659G>A | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 4/7 | chrX | 38675046 | ||||||
| chrX:38675149
|
C | G | 4 | a0001c0001t0002g0155a0001c0001t0002g0167a0001c0001t0002g0179others(1): Show | 4 | HG01071.hp1 HG01106.hp1 HG01175.hp2 others(1): Show |
intron_variant | MODIFIER | c.442-556C>G | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 4/7 | chrX | 38675149 | ||||||
| chrX:38675410
|
G | A | 174 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(171): Show | 181 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(178): Show |
intron_variant | MODIFIER | c.442-295G>A | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 4/7 | chrX | 38675410 | ||||||
| chrX:38675446
|
CAG | C | 1 | a0001c0001t0001g0128 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.442-257_442-256del others(2): Show |
TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chrX | 38675446 | |||||
| chrX:38675679
|
T | A | 1 | a0001c0002t0001g0212 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.442-26T>A | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 4/7 | chrX | 38675679 | ||||||
| chrX:38675920
|
A | G | 168 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(165): Show | 175 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(172): Show |
intron_variant | MODIFIER | c.597+60A>G | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 5/7 | chrX | 38675920 | ||||||
| chrX:38676156
|
G | A | 1 | a0001c0001t0002g0191 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.597+296G>A | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 5/7 | chrX | 38676156 | ||||||
| chrX:38676323
|
T | C | 12 | a0001c0001t0001g0056a0001c0001t0001g0060a0001c0001t0001g0077others(9): Show | 12 | HG01884.hp1 HG01891.hp2 HG02145.hp1 others(9): Show |
intron_variant | MODIFIER | c.597+463T>C | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 5/7 | chrX | 38676323 | ||||||
| chrX:38676876
|
C | T | 1 | a0001c0003t0004g0207 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.597+1016C>T | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 5/7 | chrX | 38676876 | ||||||
| chrX:38677039
|
A | G | 13 | a0001c0001t0002g0081a0001c0002t0001g0001a0001c0002t0001g0068others(10): Show | 14 | HG02109.hp2 HG02257.hp2 HG02258.hp1 others(11): Show |
intron_variant | MODIFIER | c.597+1179A>G | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 5/7 | chrX | 38677039 | ||||||
| chrX:38677067
|
C | CT | 5 | a0001c0001t0002g0081a0001c0003t0001g0181a0001c0003t0001g0200others(2): Show | 5 | HG02109.hp2 HG02258.hp1 HG02622.hp1 others(2): Show |
intron_variant | MODIFIER | c.597+1215dupT | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chrX | 38677067 | |||||
| chrX:38677343
|
T | G | 1 | a0001c0001t0002g0020 | 1 | NA19055.hp1 | intron_variant | MODIFIER | c.597+1483T>G | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 5/7 | chrX | 38677343 | ||||||
| chrX:38677429
|
G | GT | 1 | a0002c0004t0001g0173 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.597+1572dupT | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chrX | 38677429 | |||||
| chrX:38677461
|
T | TA | 1 | a0002c0004t0001g0173 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.597+1606dupA | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chrX | 38677461 | |||||
| chrX:38677470
|
GT | G | 1 | a0002c0004t0001g0173 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.597+1613delT | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chrX | 38677470 | |||||
| chrX:38677895
|
A | AG | 1 | a0002c0004t0001g0173 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.597+2037dupG | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chrX | 38677895 | |||||
| chrX:38677909
|
C | CT | 1 | a0002c0004t0001g0173 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.597+2050dupT | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chrX | 38677909 | |||||
| chrX:38677916
|
A | AT | 1 | a0002c0004t0001g0173 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.597+2058dupT | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chrX | 38677916 | |||||
| chrX:38677917
|
T | C | 3 | a0001c0001t0001g0024a0001c0001t0001g0153a0001c0001t0001g0154 | 3 | HG00099.hp1 HG02735.hp1 HG03688.hp1 |
intron_variant | MODIFIER | c.597+2057T>C | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 5/7 | chrX | 38677917 | ||||||
| chrX:38678070
|
G | GA | 1 | a0002c0004t0001g0173 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.597+2210_597+2211i others(3): Show |
TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 5/7 | chrX | 38678070 | ||||||
| chrX:38678085
|
A | AG | 1 | a0002c0004t0001g0173 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.597+2225_597+2226i others(3): Show |
TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 5/7 | chrX | 38678085 | ||||||
| chrX:38678125
|
TG | T | 1 | a0001c0001t0002g0020 | 1 | NA19055.hp1 | intron_variant | MODIFIER | c.597+2269delG | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chrX | 38678125 | |||||
| chrX:38678235
|
C | G | 2 | a0001c0001t0003g0057a0001c0001t0003g0058 | 2 | HG02976.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.597+2375C>G | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 5/7 | chrX | 38678235 | ||||||
| chrX:38678413
|
G | C | 1 | a0001c0001t0001g0169 | 1 | NA18991.hp2 | intron_variant | MODIFIER | c.597+2553G>C | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 5/7 | chrX | 38678413 | ||||||
| chrX:38678482
|
G | GA | 1 | a0002c0004t0001g0173 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.597+2625dupA | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chrX | 38678482 | |||||
| chrX:38678547
|
T | TA | 1 | a0002c0004t0001g0173 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.598-2654dupA | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chrX | 38678547 | |||||
| chrX:38678636
|
C | A | 8 | a0001c0002t0001g0001a0001c0002t0001g0068a0001c0002t0001g0074others(5): Show | 9 | HG02257.hp2 HG02559.hp2 HG02717.hp1 others(6): Show |
intron_variant | MODIFIER | c.598-2568C>A | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 5/7 | chrX | 38678636 | ||||||
| chrX:38678648
|
G | GA | 1 | a0002c0004t0001g0173 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.598-2551dupA | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chrX | 38678648 | |||||
| chrX:38678705
|
C | CA | 1 | a0002c0004t0001g0173 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.598-2492dupA | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chrX | 38678705 | |||||
| chrX:38678789
|
T | TA | 1 | a0002c0004t0001g0173 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.598-2409dupA | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chrX | 38678789 | |||||
| chrX:38679017
|
G | T | 1 | a0001c0001t0001g0211 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.598-2187G>T | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 5/7 | chrX | 38679017 | ||||||
| chrX:38679259
|
C | T | 2 | a0001c0001t0001g0129a0001c0001t0001g0164 | 2 | HG01167.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.598-1945C>T | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 5/7 | chrX | 38679259 | ||||||
| chrX:38679271
|
C | G | 24 | a0001c0001t0001g0056a0001c0001t0001g0060a0001c0001t0001g0077others(21): Show | 25 | HG01884.hp1 HG01891.hp2 HG02109.hp2 others(22): Show |
intron_variant | MODIFIER | c.598-1933C>G | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 5/7 | chrX | 38679271 | ||||||
| chrX:38679312
|
C | T | 1 | a0001c0001t0002g0130 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.598-1892C>T | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 5/7 | chrX | 38679312 | ||||||
| chrX:38679348
|
C | A | 12 | a0001c0001t0001g0056a0001c0001t0001g0060a0001c0001t0001g0077others(9): Show | 12 | HG01884.hp1 HG01891.hp2 HG02145.hp1 others(9): Show |
intron_variant | MODIFIER | c.598-1856C>A | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 5/7 | chrX | 38679348 | ||||||
| chrX:38679363
|
A | T | 8 | a0001c0002t0001g0001a0001c0002t0001g0068a0001c0002t0001g0074others(5): Show | 9 | HG02257.hp2 HG02559.hp2 HG02717.hp1 others(6): Show |
intron_variant | MODIFIER | c.598-1841A>T | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 5/7 | chrX | 38679363 | ||||||
| chrX:38679422
|
T | TTGG | 1 | a0001c0001t0002g0020 | 1 | NA19055.hp1 | intron_variant | MODIFIER | c.598-1781_598-1779d others(5): Show |
TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chrX | 38679422 | |||||
| chrX:38679499
|
CT | C | 1 | a0002c0004t0001g0173 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.598-1701delT | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chrX | 38679499 | |||||
| chrX:38679637
|
T | TA | 1 | a0002c0004t0001g0173 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.598-1562dupA | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chrX | 38679637 | |||||
| chrX:38679657
|
AG | A | 1 | a0002c0004t0001g0173 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.598-1545delG | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chrX | 38679657 | |||||
| chrX:38679720
|
C | CA | 119 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(116): Show | 124 | HG00140.hp1 HG00280.hp1 HG00438.hp2 others(121): Show |
intron_variant | MODIFIER | c.598-1474dupA | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chrX | 38679720 | |||||
| chrX:38679720
|
C | CAA | 2 | a0001c0001t0001g0055a0001c0001t0001g0082 | 2 | HG02622.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.598-1475_598-1474d others(4): Show |
TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chrX | 38679720 | |||||
| chrX:38679751
|
GA | G | 2 | a0001c0001t0001g0177a0002c0004t0001g0173 | 2 | NA18985.hp1 NA19091.hp1 |
intron_variant | MODIFIER | c.598-1444delA | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chrX | 38679751 | |||||
| chrX:38680007
|
G | GA | 1 | a0002c0004t0001g0173 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.598-1192dupA | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chrX | 38680007 | |||||
| chrX:38680007
|
GA | G | 1 | a0001c0001t0002g0020 | 1 | NA19055.hp1 | intron_variant | MODIFIER | c.598-1192delA | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chrX | 38680007 | |||||
| chrX:38680128
|
C | T | 5 | a0001c0001t0002g0151a0001c0001t0002g0155a0001c0001t0002g0167others(2): Show | 5 | HG01071.hp1 HG01106.hp1 HG01175.hp2 others(2): Show |
intron_variant | MODIFIER | c.598-1076C>T | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 5/7 | chrX | 38680128 | ||||||
| chrX:38680173
|
A | AT | 1 | a0002c0004t0001g0173 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.598-1022dupT | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chrX | 38680173 | |||||
| chrX:38680207
|
A | G | 5 | a0001c0001t0001g0003a0001c0001t0001g0119a0001c0001t0001g0123others(2): Show | 6 | HG01257.hp1 HG01975.hp2 HG01981.hp1 others(3): Show |
intron_variant | MODIFIER | c.598-997A>G | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 5/7 | chrX | 38680207 | ||||||
| chrX:38680311
|
T | G | 174 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(171): Show | 181 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(178): Show |
intron_variant | MODIFIER | c.598-893T>G | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 5/7 | chrX | 38680311 | ||||||
| chrX:38680346
|
G | A | 1 | a0001c0001t0001g0015 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.598-858G>A | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 5/7 | chrX | 38680346 | ||||||
| chrX:38680462
|
C | T | 5 | a0001c0001t0001g0075a0001c0003t0001g0181a0001c0003t0001g0200others(2): Show | 5 | HG02109.hp2 HG02258.hp1 HG02622.hp1 others(2): Show |
intron_variant | MODIFIER | c.598-742C>T | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 5/7 | chrX | 38680462 | ||||||
| chrX:38680535
|
C | G | 1 | a0001c0001t0002g0021 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.598-669C>G | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 5/7 | chrX | 38680535 | ||||||
| chrX:38680538
|
A | ATTCT | 3 | a0001c0001t0001g0077a0001c0001t0001g0084a0001c0001t0001g0211 | 3 | HG02615.hp1 HG02647.hp1 HG02723.hp1 |
intron_variant | MODIFIER | c.598-665_598-662dup others(4): Show |
TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chrX | 38680538 | |||||
| chrX:38680539
|
T | TTC | 21 | a0001c0001t0001g0003a0001c0001t0001g0008a0001c0001t0001g0035others(18): Show | 22 | HG00609.hp1 HG00642.hp1 HG01071.hp1 others(19): Show |
intron_variant | MODIFIER | c.598-621_598-620dup others(2): Show |
TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chrX | 38680539 | |||||
| chrX:38680539
|
T | TTCTC | 7 | a0001c0001t0001g0056a0001c0001t0001g0082a0001c0001t0001g0085others(4): Show | 7 | HG00438.hp2 HG02145.hp1 HG03098.hp1 others(4): Show |
intron_variant | MODIFIER | c.598-623_598-620dup others(4): Show |
TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chrX | 38680539 | |||||
| chrX:38680539
|
T | TTCTCTC | 8 | a0001c0001t0001g0040a0001c0001t0001g0053a0001c0001t0001g0086others(5): Show | 8 | HG00280.hp1 HG01099.hp1 HG02074.hp1 others(5): Show |
intron_variant | MODIFIER | c.598-625_598-620dup others(6): Show |
TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chrX | 38680539 | |||||
| chrX:38680539
|
T | TTCTCTCT others(1): Show |
2 | a0001c0001t0001g0098a0001c0001t0002g0138 | 2 | HG03704.hp2 NA19002.hp1 |
intron_variant | MODIFIER | c.598-627_598-620dup others(8): Show |
TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chrX | 38680539 | |||||
| chrX:38680539
|
T | TTCTCTCT others(3): Show |
4 | a0001c0001t0001g0038a0001c0001t0001g0059a0001c0001t0001g0071others(1): Show | 4 | HG00621.hp1 HG02055.hp1 HG02895.hp1 others(1): Show |
intron_variant | MODIFIER | c.598-629_598-620dup others(10): Show |
TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chrX | 38680539 | |||||
| chrX:38680539
|
T | TTCTCTCT others(9): Show |
1 | a0001c0001t0005g0078 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.598-635_598-620dup others(16): Show |
TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chrX | 38680539 | |||||
| chrX:38680539
|
T | TTCTTC | 1 | a0001c0001t0001g0210 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.598-662_598-661ins others(5): Show |
TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chrX | 38680539 | |||||
| chrX:38680539
|
T | TTCTTTC | 1 | a0001c0001t0001g0199 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.598-662_598-661ins others(6): Show |
TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chrX | 38680539 | |||||
| chrX:38680539
|
TTC | T | 26 | a0001c0001t0001g0005a0001c0001t0001g0014a0001c0001t0001g0045others(23): Show | 27 | HG00099.hp1 HG00438.hp1 HG01517.hp1 others(24): Show |
intron_variant | MODIFIER | c.598-621_598-620del others(2): Show |
TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chrX | 38680539 | |||||
| chrX:38680539
|
TTCTC | T | 82 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0006others(79): Show | 85 | HG00140.hp1 HG00673.hp1 HG01069.hp1 others(82): Show |
intron_variant | MODIFIER | c.598-623_598-620del others(4): Show |
TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chrX | 38680539 | |||||
| chrX:38680539
|
TTCTCTC | T | 1 | a0001c0001t0001g0090 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.598-625_598-620del others(6): Show |
TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chrX | 38680539 | |||||
| chrX:38680539
|
TTCTCTCT others(1): Show |
T | 4 | a0001c0001t0001g0139a0001c0001t0001g0147a0001c0003t0001g0181others(1): Show | 4 | HG02258.hp1 HG02622.hp1 NA18970.hp1 others(1): Show |
intron_variant | MODIFIER | c.598-627_598-620del others(8): Show |
TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chrX | 38680539 | |||||
| chrX:38680539
|
TTCTCTCT others(3): Show |
T | 2 | a0001c0001t0001g0169a0001c0003t0001g0200 | 2 | HG03471.hp1 NA18991.hp2 |
intron_variant | MODIFIER | c.598-629_598-620del others(10): Show |
TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chrX | 38680539 | |||||
| chrX:38680539
|
TTCTCTCT others(5): Show |
T | 2 | a0001c0001t0001g0036a0001c0001t0001g0135 | 2 | HG00741.hp1 NA19088.hp1 |
intron_variant | MODIFIER | c.598-631_598-620del others(12): Show |
TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chrX | 38680539 | |||||
| chrX:38680539
|
TTCTCTCT others(9): Show |
T | 1 | a0001c0001t0001g0148 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.598-635_598-620del others(16): Show |
TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chrX | 38680539 | |||||
| chrX:38680539
|
TTCTCTCT others(15): Show |
T | 8 | a0001c0002t0001g0001a0001c0002t0001g0068a0001c0002t0001g0074others(5): Show | 9 | HG02257.hp2 HG02559.hp2 HG02717.hp1 others(6): Show |
intron_variant | MODIFIER | c.598-641_598-620del others(22): Show |
TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chrX | 38680539 | |||||
| chrX:38680707
|
T | C | 2 | a0001c0003t0001g0181a0001c0003t0001g0215 | 2 | HG02258.hp1 HG02622.hp1 |
intron_variant | MODIFIER | c.598-497T>C | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 5/7 | chrX | 38680707 | ||||||
| chrX:38680796
|
G | A | 12 | a0001c0001t0001g0056a0001c0001t0001g0060a0001c0001t0001g0077others(9): Show | 12 | HG01884.hp1 HG01891.hp2 HG02145.hp1 others(9): Show |
intron_variant | MODIFIER | c.598-408G>A | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 5/7 | chrX | 38680796 | ||||||
| chrX:38680862
|
T | C | 2 | a0001c0001t0001g0059a0001c0001t0001g0071 | 2 | HG02895.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.598-342T>C | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 5/7 | chrX | 38680862 | ||||||
| chrX:38680865
|
TA | T | 1 | a0002c0004t0001g0173 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.598-336delA | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chrX | 38680865 | |||||
| chrX:38680924
|
A | C | 2 | a0001c0003t0001g0181a0001c0003t0001g0215 | 2 | HG02258.hp1 HG02622.hp1 |
intron_variant | MODIFIER | c.598-280A>C | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 5/7 | chrX | 38680924 | ||||||
| chrX:38680994
|
A | AG | 1 | a0002c0004t0001g0173 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.598-207dupG | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chrX | 38680994 | |||||
| chrX:38681009
|
T | C | 1 | a0001c0001t0001g0100 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.598-195T>C | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 5/7 | chrX | 38681009 | ||||||
| chrX:38681051
|
GT | G | 1 | a0002c0004t0001g0173 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.598-150delT | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chrX | 38681051 | |||||
| chrX:38681096
|
A | AT | 1 | a0002c0004t0001g0173 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.598-105dupT | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chrX | 38681096 | |||||
| chrX:38681103
|
G | GA | 1 | a0002c0004t0001g0173 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.598-99dupA | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chrX | 38681103 | |||||
| chrX:38681124
|
T | C | 1 | a0001c0001t0001g0114 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.598-80T>C | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 5/7 | chrX | 38681124 | ||||||
| chrX:38681166
|
G | GA | 1 | a0002c0004t0001g0173 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.598-34dupA | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chrX | 38681166 | |||||
| chrX:38681449
|
T | TTC | 1 | a0002c0004t0001g0173 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.681+163_681+164ins others(2): Show |
TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chrX | 38681449 | |||||
| chrX:38681582
|
G | A | 40 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0010others(37): Show | 42 | HG00099.hp1 HG01069.hp1 HG01071.hp2 others(39): Show |
intron_variant | MODIFIER | c.681+295G>A | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 6/7 | chrX | 38681582 | ||||||
| chrX:38681656
|
C | CT | 1 | a0002c0004t0001g0173 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.681+375dupT | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chrX | 38681656 | |||||
| chrX:38681689
|
A | G | 27 | a0001c0001t0001g0056a0001c0001t0001g0059a0001c0001t0001g0060others(24): Show | 28 | HG01884.hp1 HG01891.hp2 HG02055.hp1 others(25): Show |
intron_variant | MODIFIER | c.681+402A>G | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 6/7 | chrX | 38681689 | ||||||
| chrX:38681800
|
G | A | 8 | a0001c0001t0001g0012a0001c0001t0001g0120a0001c0001t0001g0121others(5): Show | 8 | HG01109.hp1 HG01256.hp1 HG01358.hp1 others(5): Show |
intron_variant | MODIFIER | c.681+513G>A | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 6/7 | chrX | 38681800 | ||||||
| chrX:38681843
|
T | C | 15 | a0001c0001t0001g0059a0001c0001t0001g0071a0001c0001t0001g0072others(12): Show | 16 | HG02055.hp1 HG02109.hp2 HG02257.hp2 others(13): Show |
intron_variant | MODIFIER | c.681+556T>C | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 6/7 | chrX | 38681843 | ||||||
| chrX:38681981
|
T | C | 166 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(163): Show | 173 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(170): Show |
intron_variant | MODIFIER | c.681+694T>C | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 6/7 | chrX | 38681981 | ||||||
| chrX:38682185
|
TA | T | 27 | a0001c0001t0001g0056a0001c0001t0001g0059a0001c0001t0001g0060others(24): Show | 28 | HG01884.hp1 HG01891.hp2 HG02055.hp1 others(25): Show |
intron_variant | MODIFIER | c.681+899delA | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 6/7 | chrX | 38682185 | ||||||
| chrX:38682186
|
A | AT | 1 | a0001c0001t0001g0113 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.681+906dupT | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chrX | 38682186 | |||||
| chrX:38682194
|
ATTTC | A | 2 | a0001c0001t0001g0060a0001c0001t0001g0087 | 2 | HG02922.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.681+911_681+914del others(4): Show |
TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chrX | 38682194 | |||||
| chrX:38682253
|
GCTAT | G | 1 | a0001c0001t0001g0147 | 1 | NA19006.hp1 | intron_variant | MODIFIER | c.681+969_681+972del others(4): Show |
TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chrX | 38682253 | |||||
| chrX:38682425
|
CAAA | C | 1 | a0001c0001t0002g0021 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.681+1140_681+1142d others(5): Show |
TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chrX | 38682425 | |||||
| chrX:38682671
|
A | G | 4 | a0001c0002t0001g0001a0001c0002t0001g0068a0001c0002t0001g0088others(1): Show | 5 | HG02559.hp2 HG02818.hp1 HG03195.hp1 others(2): Show |
intron_variant | MODIFIER | c.681+1384A>G | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 6/7 | chrX | 38682671 | ||||||
| chrX:38683055
|
C | G | 154 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(151): Show | 160 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(157): Show |
intron_variant | MODIFIER | c.681+1768C>G | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 6/7 | chrX | 38683055 | ||||||
| chrX:38683428
|
G | A | 1 | a0001c0003t0001g0201 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.681+2141G>A | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 6/7 | chrX | 38683428 | ||||||
| chrX:38683941
|
T | G | 3 | a0001c0001t0001g0059a0001c0001t0001g0071a0001c0001t0001g0072 | 3 | HG02055.hp1 HG02895.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.681+2654T>G | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 6/7 | chrX | 38683941 | ||||||
| chrX:38684257
|
C | G | 8 | a0001c0002t0001g0001a0001c0002t0001g0068a0001c0002t0001g0074others(5): Show | 9 | HG02257.hp2 HG02559.hp2 HG02717.hp1 others(6): Show |
intron_variant | MODIFIER | c.681+2970C>G | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 6/7 | chrX | 38684257 | ||||||
| chrX:38684349
|
CCT | C | 12 | a0001c0001t0001g0056a0001c0001t0001g0060a0001c0001t0001g0077others(9): Show | 12 | HG01884.hp1 HG01891.hp2 HG02145.hp1 others(9): Show |
intron_variant | MODIFIER | c.681+3064_681+3065d others(4): Show |
TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chrX | 38684349 | |||||
| chrX:38685120
|
T | C | 8 | a0001c0002t0001g0001a0001c0002t0001g0068a0001c0002t0001g0074others(5): Show | 9 | HG02257.hp2 HG02559.hp2 HG02717.hp1 others(6): Show |
intron_variant | MODIFIER | c.682-2479T>C | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 6/7 | chrX | 38685120 | ||||||
| chrX:38685171
|
G | A | 8 | a0001c0002t0001g0001a0001c0002t0001g0068a0001c0002t0001g0074others(5): Show | 9 | HG02257.hp2 HG02559.hp2 HG02717.hp1 others(6): Show |
intron_variant | MODIFIER | c.682-2428G>A | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 6/7 | chrX | 38685171 | ||||||
| chrX:38685276
|
GTT | G | 1 | a0001c0001t0001g0216 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.682-2320_682-2319d others(4): Show |
TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chrX | 38685276 | |||||
| chrX:38685457
|
T | A | 7 | a0001c0001t0001g0059a0001c0001t0001g0071a0001c0001t0001g0072others(4): Show | 7 | HG02055.hp1 HG02109.hp2 HG02258.hp1 others(4): Show |
intron_variant | MODIFIER | c.682-2142T>A | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 6/7 | chrX | 38685457 | ||||||
| chrX:38685620
|
G | A | 1 | a0001c0001t0001g0190 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.682-1979G>A | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 6/7 | chrX | 38685620 | ||||||
| chrX:38685674
|
G | A | 166 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(163): Show | 173 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(170): Show |
intron_variant | MODIFIER | c.682-1925G>A | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 6/7 | chrX | 38685674 | ||||||
| chrX:38685680
|
C | T | 4 | a0001c0002t0001g0001a0001c0002t0001g0068a0001c0002t0001g0088others(1): Show | 5 | HG02559.hp2 HG02818.hp1 HG03195.hp1 others(2): Show |
intron_variant | MODIFIER | c.682-1919C>T | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 6/7 | chrX | 38685680 | ||||||
| chrX:38685748
|
T | C | 1 | a0001c0001t0001g0045 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.682-1851T>C | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 6/7 | chrX | 38685748 | ||||||
| chrX:38685768
|
T | C | 139 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(136): Show | 145 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(142): Show |
intron_variant | MODIFIER | c.682-1831T>C | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 6/7 | chrX | 38685768 | ||||||
| chrX:38686651
|
G | A | 1 | a0001c0001t0002g0021 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.682-948G>A | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 6/7 | chrX | 38686651 | ||||||
| chrX:38686975
|
C | T | 1 | a0001c0001t0001g0075 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.682-624C>T | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 6/7 | chrX | 38686975 | ||||||
| chrX:38687026
|
A | G | 12 | a0001c0001t0001g0056a0001c0001t0001g0060a0001c0001t0001g0077others(9): Show | 12 | HG01884.hp1 HG01891.hp2 HG02145.hp1 others(9): Show |
intron_variant | MODIFIER | c.682-573A>G | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 6/7 | chrX | 38687026 | ||||||
| chrX:38687140
|
A | G | 1 | a0001c0001t0002g0182 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.682-459A>G | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 6/7 | chrX | 38687140 | ||||||
| chrX:38687231
|
CTTAA | C | 1 | a0001c0001t0002g0155 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.682-365_682-362del others(4): Show |
TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chrX | 38687231 | |||||
| chrX:38687572
|
C | T | 12 | a0001c0001t0001g0056a0001c0001t0001g0060a0001c0001t0001g0077others(9): Show | 12 | HG01884.hp1 HG01891.hp2 HG02145.hp1 others(9): Show |
intron_variant | MODIFIER | c.682-27C>T | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 6/7 | chrX | 38687572 | ||||||
| chrX:38687755
|
C | T | 1 | a0001c0001t0001g0060 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.*7+81C>T | TSPAN7 | ENSG00000156298.13 | transcript | ENST00000378482.7 | protein_coding | 7/7 | chrX | 38687755 |