Search by Gene
| geneid | 158747 |
|---|---|
| ensemblid | ENSG00000130150.12 |
| hgncid | 28381 |
| symbol | MOSPD2 |
| name | motile sperm domain containing 2 |
| refseq_nuc | NM_152581.4 |
| refseq_prot | NP_689794.1 |
| ensembl_nuc | ENST00000380492.8 |
| ensembl_prot | ENSP00000369860.3 |
| mane_status | MANE Select |
| chr | chrX |
| start | 14873421 |
| end | 14922327 |
| strand | + |
| ver | v1.2 |
| region | chrX:14873421-14922327 |
| region5000 | chrX:14868421-14927327 |
| regionname0 | MOSPD2_chrX_14873421_14922327 |
| regionname5000 | MOSPD2_chrX_14868421_14927327 |
Multiple Alignments (by translate haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
Multiple Alignments (by aa haplotype frequency)
| 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 | regionname | genename | aa |
|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 518 | 264 | 78 | 55 | 101 | 5 | 23 | MOSPD2_chrX_14868421_14927327 | MOSPD2 | copy fasta |
| a0002 | 0/0 | 518 | 4 | 0 | 1 | 0 | 2 | 1 | MOSPD2_chrX_14868421_14927327 | MOSPD2 | copy fasta |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|
| c0001 | 1/1 | 1557 | 260 | 77 | 52 | 101 | 5 | 23 | MOSPD2_chrX_14868421_14927327 | MOSPD2 | copy fasta |
| c0002 | 0/0 | 1557 | 4 | 0 | 1 | 0 | 2 | 1 | MOSPD2_chrX_14868421_14927327 | MOSPD2 | copy fasta |
| c0003 | 0/0 | 1557 | 3 | 0 | 3 | 0 | 0 | 0 | MOSPD2_chrX_14868421_14927327 | MOSPD2 | copy fasta |
| c0004 | 0/0 | 1557 | 1 | 1 | 0 | 0 | 0 | 0 | MOSPD2_chrX_14868421_14927327 | MOSPD2 | copy fasta |
| thapid | 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
|
tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq |
|---|---|---|---|---|---|---|---|---|---|---|---|
| t0001 | 1/1 | 2627 | 225 | 46 | 46 | 101 | 7 | 23 | MOSPD2_chrX_14868421_14927327 | MOSPD2 | copy fasta |
| t0002 | 0/0 | 2627 | 17 | 15 | 2 | 0 | 0 | 0 | MOSPD2_chrX_14868421_14927327 | MOSPD2 | copy fasta |
| t0003 | 0/0 | 2626 | 14 | 12 | 2 | 0 | 0 | 0 | MOSPD2_chrX_14868421_14927327 | MOSPD2 | copy fasta |
| t0004 | 0/0 | 2627 | 3 | 3 | 0 | 0 | 0 | 0 | MOSPD2_chrX_14868421_14927327 | MOSPD2 | copy fasta |
| t0005 | 0/0 | 2627 | 2 | 0 | 2 | 0 | 0 | 0 | MOSPD2_chrX_14868421_14927327 | MOSPD2 | copy fasta |
| t0006 | 0/0 | 2627 | 1 | 0 | 1 | 0 | 0 | 0 | MOSPD2_chrX_14868421_14927327 | MOSPD2 | copy fasta |
| t0007 | 0/0 | 2627 | 1 | 0 | 0 | 0 | 0 | 1 | MOSPD2_chrX_14868421_14927327 | MOSPD2 | copy fasta |
| t0008 | 0/0 | 2622 | 1 | 1 | 0 | 0 | 0 | 0 | MOSPD2_chrX_14868421_14927327 | MOSPD2 | copy fasta |
| t0009 | 0/0 | 2631 | 1 | 0 | 1 | 0 | 0 | 0 | MOSPD2_chrX_14868421_14927327 | MOSPD2 | copy fasta |
| t0010 | 0/0 | 2627 | 1 | 0 | 1 | 0 | 0 | 0 | MOSPD2_chrX_14868421_14927327 | MOSPD2 | copy fasta |
| t0011 | 0/0 | 2626 | 1 | 1 | 0 | 0 | 0 | 0 | MOSPD2_chrX_14868421_14927327 | MOSPD2 | copy fasta |
| t0012 | 0/0 | 2627 | 1 | 0 | 1 | 0 | 0 | 0 | MOSPD2_chrX_14868421_14927327 | MOSPD2 | copy fasta |
| 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 |
|---|---|---|---|---|---|---|---|---|---|
| g0001 | 0/0 | 15 | 1 | 4 | 10 | 0 | 0 | MOSPD2_chrX_14868421_14927327 | MOSPD2 |
| g0002 | 0/0 | 9 | 0 | 1 | 7 | 0 | 1 | MOSPD2_chrX_14868421_14927327 | MOSPD2 |
| g0003 | 0/0 | 4 | 3 | 1 | 0 | 0 | 0 | MOSPD2_chrX_14868421_14927327 | MOSPD2 |
| g0004 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | MOSPD2_chrX_14868421_14927327 | MOSPD2 |
| g0005 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | MOSPD2_chrX_14868421_14927327 | MOSPD2 |
| g0006 | 0/0 | 3 | 2 | 1 | 0 | 0 | 0 | MOSPD2_chrX_14868421_14927327 | MOSPD2 |
| g0007 | 0/0 | 3 | 2 | 1 | 0 | 0 | 0 | MOSPD2_chrX_14868421_14927327 | MOSPD2 |
| g0008 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | MOSPD2_chrX_14868421_14927327 | MOSPD2 |
| g0009 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | MOSPD2_chrX_14868421_14927327 | MOSPD2 |
| g0010 | 0/0 | 3 | 0 | 1 | 2 | 0 | 0 | MOSPD2_chrX_14868421_14927327 | MOSPD2 |
| g0011 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MOSPD2_chrX_14868421_14927327 | MOSPD2 |
| g0012 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MOSPD2_chrX_14868421_14927327 | MOSPD2 |
| g0013 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MOSPD2_chrX_14868421_14927327 | MOSPD2 |
| g0014 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | MOSPD2_chrX_14868421_14927327 | MOSPD2 |
| g0015 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MOSPD2_chrX_14868421_14927327 | MOSPD2 |
| g0016 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MOSPD2_chrX_14868421_14927327 | MOSPD2 |
| g0017 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | MOSPD2_chrX_14868421_14927327 | MOSPD2 |
| g0018 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | MOSPD2_chrX_14868421_14927327 | MOSPD2 |
| g0019 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | MOSPD2_chrX_14868421_14927327 | MOSPD2 |
| g0020 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | MOSPD2_chrX_14868421_14927327 | MOSPD2 |
| g0021 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MOSPD2_chrX_14868421_14927327 | MOSPD2 |
| g0022 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MOSPD2_chrX_14868421_14927327 | MOSPD2 |
| g0023 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | MOSPD2_chrX_14868421_14927327 | MOSPD2 |
| g0024 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | MOSPD2_chrX_14868421_14927327 | MOSPD2 |
| g0025 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | MOSPD2_chrX_14868421_14927327 | MOSPD2 |
| g0026 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MOSPD2_chrX_14868421_14927327 | MOSPD2 |
| g0027 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | MOSPD2_chrX_14868421_14927327 | MOSPD2 |
| g0028 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MOSPD2_chrX_14868421_14927327 | MOSPD2 |
| g0029 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MOSPD2_chrX_14868421_14927327 | MOSPD2 |
| g0030 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MOSPD2_chrX_14868421_14927327 | MOSPD2 |
| g0031 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MOSPD2_chrX_14868421_14927327 | MOSPD2 |
| g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MOSPD2_chrX_14868421_14927327 | MOSPD2 |
| g0033 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MOSPD2_chrX_14868421_14927327 | MOSPD2 |
| g0034 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MOSPD2_chrX_14868421_14927327 | MOSPD2 |
| g0035 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MOSPD2_chrX_14868421_14927327 | MOSPD2 |
| g0036 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MOSPD2_chrX_14868421_14927327 | MOSPD2 |
| g0037 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MOSPD2_chrX_14868421_14927327 | MOSPD2 |
| g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MOSPD2_chrX_14868421_14927327 | MOSPD2 |
| g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MOSPD2_chrX_14868421_14927327 | MOSPD2 |
| g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MOSPD2_chrX_14868421_14927327 | MOSPD2 |
| g0041 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MOSPD2_chrX_14868421_14927327 | MOSPD2 |
| g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MOSPD2_chrX_14868421_14927327 | MOSPD2 |
| g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MOSPD2_chrX_14868421_14927327 | MOSPD2 |
| g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MOSPD2_chrX_14868421_14927327 | MOSPD2 |
| g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MOSPD2_chrX_14868421_14927327 | MOSPD2 |
| g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MOSPD2_chrX_14868421_14927327 | MOSPD2 |
| g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MOSPD2_chrX_14868421_14927327 | MOSPD2 |
| g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MOSPD2_chrX_14868421_14927327 | MOSPD2 |
| g0049 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MOSPD2_chrX_14868421_14927327 | MOSPD2 |
| g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MOSPD2_chrX_14868421_14927327 | MOSPD2 |
| g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MOSPD2_chrX_14868421_14927327 | MOSPD2 |
| g0052 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MOSPD2_chrX_14868421_14927327 | MOSPD2 |
| g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MOSPD2_chrX_14868421_14927327 | MOSPD2 |
| g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MOSPD2_chrX_14868421_14927327 | MOSPD2 |
| g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MOSPD2_chrX_14868421_14927327 | MOSPD2 |
| g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MOSPD2_chrX_14868421_14927327 | MOSPD2 |
| g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MOSPD2_chrX_14868421_14927327 | MOSPD2 |
| g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MOSPD2_chrX_14868421_14927327 | MOSPD2 |
| g0059 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MOSPD2_chrX_14868421_14927327 | MOSPD2 |
| g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MOSPD2_chrX_14868421_14927327 | MOSPD2 |
| g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MOSPD2_chrX_14868421_14927327 | MOSPD2 |
| g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MOSPD2_chrX_14868421_14927327 | MOSPD2 |
| g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MOSPD2_chrX_14868421_14927327 | MOSPD2 |
| g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MOSPD2_chrX_14868421_14927327 | MOSPD2 |
| g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MOSPD2_chrX_14868421_14927327 | MOSPD2 |
| g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MOSPD2_chrX_14868421_14927327 | MOSPD2 |
| g0067 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MOSPD2_chrX_14868421_14927327 | MOSPD2 |
| g0068 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MOSPD2_chrX_14868421_14927327 | MOSPD2 |
| g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MOSPD2_chrX_14868421_14927327 | MOSPD2 |
| g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MOSPD2_chrX_14868421_14927327 | MOSPD2 |
| g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MOSPD2_chrX_14868421_14927327 | MOSPD2 |
| g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MOSPD2_chrX_14868421_14927327 | MOSPD2 |
| g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MOSPD2_chrX_14868421_14927327 | MOSPD2 |
| g0074 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MOSPD2_chrX_14868421_14927327 | MOSPD2 |
| g0075 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MOSPD2_chrX_14868421_14927327 | MOSPD2 |
| g0076 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MOSPD2_chrX_14868421_14927327 | MOSPD2 |
| g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MOSPD2_chrX_14868421_14927327 | MOSPD2 |
| g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MOSPD2_chrX_14868421_14927327 | MOSPD2 |
| g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MOSPD2_chrX_14868421_14927327 | MOSPD2 |
| g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MOSPD2_chrX_14868421_14927327 | MOSPD2 |
| g0081 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MOSPD2_chrX_14868421_14927327 | MOSPD2 |
| g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MOSPD2_chrX_14868421_14927327 | MOSPD2 |
| g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MOSPD2_chrX_14868421_14927327 | MOSPD2 |
| g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MOSPD2_chrX_14868421_14927327 | MOSPD2 |
| g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MOSPD2_chrX_14868421_14927327 | MOSPD2 |
| g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MOSPD2_chrX_14868421_14927327 | MOSPD2 |
| g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MOSPD2_chrX_14868421_14927327 | MOSPD2 |
| g0088 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MOSPD2_chrX_14868421_14927327 | MOSPD2 |
| g0089 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MOSPD2_chrX_14868421_14927327 | MOSPD2 |
| g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MOSPD2_chrX_14868421_14927327 | MOSPD2 |
| g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MOSPD2_chrX_14868421_14927327 | MOSPD2 |
| g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MOSPD2_chrX_14868421_14927327 | MOSPD2 |
| g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MOSPD2_chrX_14868421_14927327 | MOSPD2 |
| g0094 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MOSPD2_chrX_14868421_14927327 | MOSPD2 |
| g0095 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MOSPD2_chrX_14868421_14927327 | MOSPD2 |
| g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MOSPD2_chrX_14868421_14927327 | MOSPD2 |
| g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MOSPD2_chrX_14868421_14927327 | MOSPD2 |
| g0098 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MOSPD2_chrX_14868421_14927327 | MOSPD2 |
| g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MOSPD2_chrX_14868421_14927327 | MOSPD2 |
| g0100 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MOSPD2_chrX_14868421_14927327 | MOSPD2 |
| g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MOSPD2_chrX_14868421_14927327 | MOSPD2 |
| g0102 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MOSPD2_chrX_14868421_14927327 | MOSPD2 |
| g0103 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MOSPD2_chrX_14868421_14927327 | MOSPD2 |
| g0104 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MOSPD2_chrX_14868421_14927327 | MOSPD2 |
| g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MOSPD2_chrX_14868421_14927327 | MOSPD2 |
| g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MOSPD2_chrX_14868421_14927327 | MOSPD2 |
| g0107 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MOSPD2_chrX_14868421_14927327 | MOSPD2 |
| g0108 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MOSPD2_chrX_14868421_14927327 | MOSPD2 |
| g0109 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MOSPD2_chrX_14868421_14927327 | MOSPD2 |
| g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MOSPD2_chrX_14868421_14927327 | MOSPD2 |
| g0111 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MOSPD2_chrX_14868421_14927327 | MOSPD2 |
| g0112 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MOSPD2_chrX_14868421_14927327 | MOSPD2 |
| g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MOSPD2_chrX_14868421_14927327 | MOSPD2 |
| g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MOSPD2_chrX_14868421_14927327 | MOSPD2 |
| g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MOSPD2_chrX_14868421_14927327 | MOSPD2 |
| g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MOSPD2_chrX_14868421_14927327 | MOSPD2 |
| g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MOSPD2_chrX_14868421_14927327 | MOSPD2 |
| g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MOSPD2_chrX_14868421_14927327 | MOSPD2 |
| g0119 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MOSPD2_chrX_14868421_14927327 | MOSPD2 |
| g0120 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MOSPD2_chrX_14868421_14927327 | MOSPD2 |
| g0121 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MOSPD2_chrX_14868421_14927327 | MOSPD2 |
| g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MOSPD2_chrX_14868421_14927327 | MOSPD2 |
| g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MOSPD2_chrX_14868421_14927327 | MOSPD2 |
| g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MOSPD2_chrX_14868421_14927327 | MOSPD2 |
| g0125 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | MOSPD2_chrX_14868421_14927327 | MOSPD2 |
| g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MOSPD2_chrX_14868421_14927327 | MOSPD2 |
| g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MOSPD2_chrX_14868421_14927327 | MOSPD2 |
| g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MOSPD2_chrX_14868421_14927327 | MOSPD2 |
| g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MOSPD2_chrX_14868421_14927327 | MOSPD2 |
| g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MOSPD2_chrX_14868421_14927327 | MOSPD2 |
| g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MOSPD2_chrX_14868421_14927327 | MOSPD2 |
| g0132 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MOSPD2_chrX_14868421_14927327 | MOSPD2 |
| g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MOSPD2_chrX_14868421_14927327 | MOSPD2 |
| g0134 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MOSPD2_chrX_14868421_14927327 | MOSPD2 |
| g0135 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MOSPD2_chrX_14868421_14927327 | MOSPD2 |
| g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MOSPD2_chrX_14868421_14927327 | MOSPD2 |
| g0137 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MOSPD2_chrX_14868421_14927327 | MOSPD2 |
| g0138 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MOSPD2_chrX_14868421_14927327 | MOSPD2 |
| g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MOSPD2_chrX_14868421_14927327 | MOSPD2 |
| g0140 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MOSPD2_chrX_14868421_14927327 | MOSPD2 |
| g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MOSPD2_chrX_14868421_14927327 | MOSPD2 |
| g0142 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MOSPD2_chrX_14868421_14927327 | MOSPD2 |
| g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MOSPD2_chrX_14868421_14927327 | MOSPD2 |
| g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MOSPD2_chrX_14868421_14927327 | MOSPD2 |
| g0145 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MOSPD2_chrX_14868421_14927327 | MOSPD2 |
| g0146 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MOSPD2_chrX_14868421_14927327 | MOSPD2 |
| g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MOSPD2_chrX_14868421_14927327 | MOSPD2 |
| g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MOSPD2_chrX_14868421_14927327 | MOSPD2 |
| g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MOSPD2_chrX_14868421_14927327 | MOSPD2 |
| g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MOSPD2_chrX_14868421_14927327 | MOSPD2 |
| g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MOSPD2_chrX_14868421_14927327 | MOSPD2 |
| g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MOSPD2_chrX_14868421_14927327 | MOSPD2 |
| g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MOSPD2_chrX_14868421_14927327 | MOSPD2 |
| g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MOSPD2_chrX_14868421_14927327 | MOSPD2 |
| g0155 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MOSPD2_chrX_14868421_14927327 | MOSPD2 |
| g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MOSPD2_chrX_14868421_14927327 | MOSPD2 |
| g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MOSPD2_chrX_14868421_14927327 | MOSPD2 |
| g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MOSPD2_chrX_14868421_14927327 | MOSPD2 |
| g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MOSPD2_chrX_14868421_14927327 | MOSPD2 |
| g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MOSPD2_chrX_14868421_14927327 | MOSPD2 |
| g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MOSPD2_chrX_14868421_14927327 | MOSPD2 |
| g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MOSPD2_chrX_14868421_14927327 | MOSPD2 |
| g0163 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MOSPD2_chrX_14868421_14927327 | MOSPD2 |
| g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MOSPD2_chrX_14868421_14927327 | MOSPD2 |
| g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MOSPD2_chrX_14868421_14927327 | MOSPD2 |
| g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MOSPD2_chrX_14868421_14927327 | MOSPD2 |
| g0167 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MOSPD2_chrX_14868421_14927327 | MOSPD2 |
| g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MOSPD2_chrX_14868421_14927327 | MOSPD2 |
| g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MOSPD2_chrX_14868421_14927327 | MOSPD2 |
| g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MOSPD2_chrX_14868421_14927327 | MOSPD2 |
| g0171 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | MOSPD2_chrX_14868421_14927327 | MOSPD2 |
| g0172 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MOSPD2_chrX_14868421_14927327 | MOSPD2 |
| g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MOSPD2_chrX_14868421_14927327 | MOSPD2 |
| g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MOSPD2_chrX_14868421_14927327 | MOSPD2 |
| g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MOSPD2_chrX_14868421_14927327 | MOSPD2 |
| g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MOSPD2_chrX_14868421_14927327 | MOSPD2 |
| g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MOSPD2_chrX_14868421_14927327 | MOSPD2 |
| g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MOSPD2_chrX_14868421_14927327 | MOSPD2 |
| g0179 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MOSPD2_chrX_14868421_14927327 | MOSPD2 |
| g0180 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MOSPD2_chrX_14868421_14927327 | MOSPD2 |
| g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MOSPD2_chrX_14868421_14927327 | MOSPD2 |
| g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MOSPD2_chrX_14868421_14927327 | MOSPD2 |
| g0183 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MOSPD2_chrX_14868421_14927327 | MOSPD2 |
| g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MOSPD2_chrX_14868421_14927327 | MOSPD2 |
| g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MOSPD2_chrX_14868421_14927327 | MOSPD2 |
| g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MOSPD2_chrX_14868421_14927327 | MOSPD2 |
| g0187 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MOSPD2_chrX_14868421_14927327 | MOSPD2 |
| g0188 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MOSPD2_chrX_14868421_14927327 | MOSPD2 |
| g0189 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MOSPD2_chrX_14868421_14927327 | MOSPD2 |
| g0190 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MOSPD2_chrX_14868421_14927327 | MOSPD2 |
| g0191 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MOSPD2_chrX_14868421_14927327 | MOSPD2 |
| g0192 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MOSPD2_chrX_14868421_14927327 | MOSPD2 |
| g0193 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MOSPD2_chrX_14868421_14927327 | MOSPD2 |
| g0194 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MOSPD2_chrX_14868421_14927327 | MOSPD2 |
| g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MOSPD2_chrX_14868421_14927327 | MOSPD2 |
| g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MOSPD2_chrX_14868421_14927327 | MOSPD2 |
| g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MOSPD2_chrX_14868421_14927327 | MOSPD2 |
| g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MOSPD2_chrX_14868421_14927327 | MOSPD2 |
| g0199 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MOSPD2_chrX_14868421_14927327 | MOSPD2 |
| g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MOSPD2_chrX_14868421_14927327 | MOSPD2 |
| g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MOSPD2_chrX_14868421_14927327 | MOSPD2 |
| g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MOSPD2_chrX_14868421_14927327 | MOSPD2 |
| g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MOSPD2_chrX_14868421_14927327 | MOSPD2 |
| g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MOSPD2_chrX_14868421_14927327 | MOSPD2 |
| g0205 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MOSPD2_chrX_14868421_14927327 | MOSPD2 |
| g0206 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MOSPD2_chrX_14868421_14927327 | MOSPD2 |
| achapid | ahapid | 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 |
total | AFR | AMR | EAS | EUR | SAS | regionname | genename | acseq |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | a0001 | c0001 | 1/1 | 260 | 77 | 52 | 101 | 5 | 23 | MOSPD2_chrX_14868421_14927327 | MOSPD2 | copy fasta |
| a0001c0003 | a0001 | c0003 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | MOSPD2_chrX_14868421_14927327 | MOSPD2 | copy fasta |
| a0001c0004 | a0001 | c0004 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MOSPD2_chrX_14868421_14927327 | MOSPD2 | copy fasta |
| a0002c0002 | a0002 | c0002 | 0/0 | 4 | 0 | 1 | 0 | 2 | 1 | MOSPD2_chrX_14868421_14927327 | MOSPD2 | copy fasta |
| acthapid | ahapid | chapid | thapid | 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 | actseq |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | a0001 | c0001 | t0001 | 1/1 | 217 | 45 | 42 | 101 | 5 | 22 | MOSPD2_chrX_14868421_14927327 | MOSPD2 | copy fasta |
| a0001c0001t0002 | a0001 | c0001 | t0002 | 0/0 | 17 | 15 | 2 | 0 | 0 | 0 | MOSPD2_chrX_14868421_14927327 | MOSPD2 | copy fasta |
| a0001c0001t0003 | a0001 | c0001 | t0003 | 0/0 | 14 | 12 | 2 | 0 | 0 | 0 | MOSPD2_chrX_14868421_14927327 | MOSPD2 | copy fasta |
| a0001c0001t0004 | a0001 | c0001 | t0004 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | MOSPD2_chrX_14868421_14927327 | MOSPD2 | copy fasta |
| a0001c0001t0005 | a0001 | c0001 | t0005 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | MOSPD2_chrX_14868421_14927327 | MOSPD2 | copy fasta |
| a0001c0001t0006 | a0001 | c0001 | t0006 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MOSPD2_chrX_14868421_14927327 | MOSPD2 | copy fasta |
| a0001c0001t0007 | a0001 | c0001 | t0007 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MOSPD2_chrX_14868421_14927327 | MOSPD2 | copy fasta |
| a0001c0001t0008 | a0001 | c0001 | t0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MOSPD2_chrX_14868421_14927327 | MOSPD2 | copy fasta |
| a0001c0001t0009 | a0001 | c0001 | t0009 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MOSPD2_chrX_14868421_14927327 | MOSPD2 | copy fasta |
| a0001c0001t0010 | a0001 | c0001 | t0010 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MOSPD2_chrX_14868421_14927327 | MOSPD2 | copy fasta |
| a0001c0001t0011 | a0001 | c0001 | t0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MOSPD2_chrX_14868421_14927327 | MOSPD2 | copy fasta |
| a0001c0001t0012 | a0001 | c0001 | t0012 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MOSPD2_chrX_14868421_14927327 | MOSPD2 | copy fasta |
| a0001c0003t0001 | a0001 | c0003 | t0001 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | MOSPD2_chrX_14868421_14927327 | MOSPD2 | copy fasta |
| a0001c0004t0001 | a0001 | c0004 | t0001 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MOSPD2_chrX_14868421_14927327 | MOSPD2 | copy fasta |
| a0002c0002t0001 | a0002 | c0002 | t0001 | 0/0 | 4 | 0 | 1 | 0 | 2 | 1 | MOSPD2_chrX_14868421_14927327 | MOSPD2 | copy fasta |
| actghapid | ahapid | chapid | thapid | 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | a0001 | c0001 | t0001 | g0001 | 0/0 | 15 | 1 | 4 | 10 | 0 | 0 | MOSPD2_chrX_14868421_14927327 | MOSPD2 |
| a0001c0001t0001g0002 | a0001 | c0001 | t0001 | g0002 | 0/0 | 9 | 0 | 1 | 7 | 0 | 1 | MOSPD2_chrX_14868421_14927327 | MOSPD2 |
| a0001c0001t0001g0004 | a0001 | c0001 | t0001 | g0004 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | MOSPD2_chrX_14868421_14927327 | MOSPD2 |
| a0001c0001t0001g0008 | a0001 | c0001 | t0001 | g0008 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | MOSPD2_chrX_14868421_14927327 | MOSPD2 |
| a0001c0001t0001g0009 | a0001 | c0001 | t0001 | g0009 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | MOSPD2_chrX_14868421_14927327 | MOSPD2 |
| a0001c0001t0001g0010 | a0001 | c0001 | t0001 | g0010 | 0/0 | 3 | 0 | 1 | 2 | 0 | 0 | MOSPD2_chrX_14868421_14927327 | MOSPD2 |
| a0001c0001t0001g0013 | a0001 | c0001 | t0001 | g0013 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MOSPD2_chrX_14868421_14927327 | MOSPD2 |
| a0001c0001t0001g0014 | a0001 | c0001 | t0001 | g0014 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MOSPD2_chrX_14868421_14927327 | MOSPD2 |
| a0001c0001t0001g0015 | a0001 | c0001 | t0001 | g0015 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MOSPD2_chrX_14868421_14927327 | MOSPD2 |
| a0001c0001t0001g0016 | a0001 | c0001 | t0001 | g0016 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MOSPD2_chrX_14868421_14927327 | MOSPD2 |
| a0001c0001t0001g0017 | a0001 | c0001 | t0001 | g0017 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | MOSPD2_chrX_14868421_14927327 | MOSPD2 |
| a0001c0001t0001g0019 | a0001 | c0001 | t0001 | g0019 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | MOSPD2_chrX_14868421_14927327 | MOSPD2 |
| a0001c0001t0001g0020 | a0001 | c0001 | t0001 | g0020 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | MOSPD2_chrX_14868421_14927327 | MOSPD2 |
| a0001c0001t0001g0021 | a0001 | c0001 | t0001 | g0021 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MOSPD2_chrX_14868421_14927327 | MOSPD2 |
| a0001c0001t0001g0022 | a0001 | c0001 | t0001 | g0022 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MOSPD2_chrX_14868421_14927327 | MOSPD2 |
| a0001c0001t0001g0024 | a0001 | c0001 | t0001 | g0024 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | MOSPD2_chrX_14868421_14927327 | MOSPD2 |
| a0001c0001t0001g0025 | a0001 | c0001 | t0001 | g0025 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | MOSPD2_chrX_14868421_14927327 | MOSPD2 |
| a0001c0001t0001g0027 | a0001 | c0001 | t0001 | g0027 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | MOSPD2_chrX_14868421_14927327 | MOSPD2 |
| a0001c0001t0001g0028 | a0001 | c0001 | t0001 | g0028 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MOSPD2_chrX_14868421_14927327 | MOSPD2 |
| a0001c0001t0001g0029 | a0001 | c0001 | t0001 | g0029 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MOSPD2_chrX_14868421_14927327 | MOSPD2 |
| a0001c0001t0001g0030 | a0001 | c0001 | t0001 | g0030 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MOSPD2_chrX_14868421_14927327 | MOSPD2 |
| a0001c0001t0001g0032 | a0001 | c0001 | t0001 | g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MOSPD2_chrX_14868421_14927327 | MOSPD2 |
| a0001c0001t0001g0038 | a0001 | c0001 | t0001 | g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MOSPD2_chrX_14868421_14927327 | MOSPD2 |
| a0001c0001t0001g0042 | a0001 | c0001 | t0001 | g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MOSPD2_chrX_14868421_14927327 | MOSPD2 |
| a0001c0001t0001g0043 | a0001 | c0001 | t0001 | g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MOSPD2_chrX_14868421_14927327 | MOSPD2 |
| a0001c0001t0001g0044 | a0001 | c0001 | t0001 | g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MOSPD2_chrX_14868421_14927327 | MOSPD2 |
| a0001c0001t0001g0045 | a0001 | c0001 | t0001 | g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MOSPD2_chrX_14868421_14927327 | MOSPD2 |
| a0001c0001t0001g0046 | a0001 | c0001 | t0001 | g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MOSPD2_chrX_14868421_14927327 | MOSPD2 |
| a0001c0001t0001g0047 | a0001 | c0001 | t0001 | g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MOSPD2_chrX_14868421_14927327 | MOSPD2 |
| a0001c0001t0001g0048 | a0001 | c0001 | t0001 | g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MOSPD2_chrX_14868421_14927327 | MOSPD2 |
| a0001c0001t0001g0049 | a0001 | c0001 | t0001 | g0049 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MOSPD2_chrX_14868421_14927327 | MOSPD2 |
| a0001c0001t0001g0050 | a0001 | c0001 | t0001 | g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MOSPD2_chrX_14868421_14927327 | MOSPD2 |
| a0001c0001t0001g0051 | a0001 | c0001 | t0001 | g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MOSPD2_chrX_14868421_14927327 | MOSPD2 |
| a0001c0001t0001g0052 | a0001 | c0001 | t0001 | g0052 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MOSPD2_chrX_14868421_14927327 | MOSPD2 |
| a0001c0001t0001g0053 | a0001 | c0001 | t0001 | g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MOSPD2_chrX_14868421_14927327 | MOSPD2 |
| a0001c0001t0001g0054 | a0001 | c0001 | t0001 | g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MOSPD2_chrX_14868421_14927327 | MOSPD2 |
| a0001c0001t0001g0055 | a0001 | c0001 | t0001 | g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MOSPD2_chrX_14868421_14927327 | MOSPD2 |
| a0001c0001t0001g0056 | a0001 | c0001 | t0001 | g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MOSPD2_chrX_14868421_14927327 | MOSPD2 |
| a0001c0001t0001g0057 | a0001 | c0001 | t0001 | g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MOSPD2_chrX_14868421_14927327 | MOSPD2 |
| a0001c0001t0001g0058 | a0001 | c0001 | t0001 | g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MOSPD2_chrX_14868421_14927327 | MOSPD2 |
| a0001c0001t0001g0059 | a0001 | c0001 | t0001 | g0059 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MOSPD2_chrX_14868421_14927327 | MOSPD2 |
| a0001c0001t0001g0060 | a0001 | c0001 | t0001 | g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MOSPD2_chrX_14868421_14927327 | MOSPD2 |
| a0001c0001t0001g0061 | a0001 | c0001 | t0001 | g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MOSPD2_chrX_14868421_14927327 | MOSPD2 |
| a0001c0001t0001g0062 | a0001 | c0001 | t0001 | g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MOSPD2_chrX_14868421_14927327 | MOSPD2 |
| a0001c0001t0001g0063 | a0001 | c0001 | t0001 | g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MOSPD2_chrX_14868421_14927327 | MOSPD2 |
| a0001c0001t0001g0064 | a0001 | c0001 | t0001 | g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MOSPD2_chrX_14868421_14927327 | MOSPD2 |
| a0001c0001t0001g0065 | a0001 | c0001 | t0001 | g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MOSPD2_chrX_14868421_14927327 | MOSPD2 |
| a0001c0001t0001g0066 | a0001 | c0001 | t0001 | g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MOSPD2_chrX_14868421_14927327 | MOSPD2 |
| a0001c0001t0001g0067 | a0001 | c0001 | t0001 | g0067 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MOSPD2_chrX_14868421_14927327 | MOSPD2 |
| a0001c0001t0001g0068 | a0001 | c0001 | t0001 | g0068 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MOSPD2_chrX_14868421_14927327 | MOSPD2 |
| a0001c0001t0001g0069 | a0001 | c0001 | t0001 | g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MOSPD2_chrX_14868421_14927327 | MOSPD2 |
| a0001c0001t0001g0070 | a0001 | c0001 | t0001 | g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MOSPD2_chrX_14868421_14927327 | MOSPD2 |
| a0001c0001t0001g0071 | a0001 | c0001 | t0001 | g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MOSPD2_chrX_14868421_14927327 | MOSPD2 |
| a0001c0001t0001g0072 | a0001 | c0001 | t0001 | g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MOSPD2_chrX_14868421_14927327 | MOSPD2 |
| a0001c0001t0001g0073 | a0001 | c0001 | t0001 | g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MOSPD2_chrX_14868421_14927327 | MOSPD2 |
| a0001c0001t0001g0074 | a0001 | c0001 | t0001 | g0074 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MOSPD2_chrX_14868421_14927327 | MOSPD2 |
| a0001c0001t0001g0075 | a0001 | c0001 | t0001 | g0075 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MOSPD2_chrX_14868421_14927327 | MOSPD2 |
| a0001c0001t0001g0076 | a0001 | c0001 | t0001 | g0076 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MOSPD2_chrX_14868421_14927327 | MOSPD2 |
| a0001c0001t0001g0077 | a0001 | c0001 | t0001 | g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MOSPD2_chrX_14868421_14927327 | MOSPD2 |
| a0001c0001t0001g0078 | a0001 | c0001 | t0001 | g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MOSPD2_chrX_14868421_14927327 | MOSPD2 |
| a0001c0001t0001g0079 | a0001 | c0001 | t0001 | g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MOSPD2_chrX_14868421_14927327 | MOSPD2 |
| a0001c0001t0001g0080 | a0001 | c0001 | t0001 | g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MOSPD2_chrX_14868421_14927327 | MOSPD2 |
| a0001c0001t0001g0081 | a0001 | c0001 | t0001 | g0081 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MOSPD2_chrX_14868421_14927327 | MOSPD2 |
| a0001c0001t0001g0082 | a0001 | c0001 | t0001 | g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MOSPD2_chrX_14868421_14927327 | MOSPD2 |
| a0001c0001t0001g0083 | a0001 | c0001 | t0001 | g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MOSPD2_chrX_14868421_14927327 | MOSPD2 |
| a0001c0001t0001g0084 | a0001 | c0001 | t0001 | g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MOSPD2_chrX_14868421_14927327 | MOSPD2 |
| a0001c0001t0001g0085 | a0001 | c0001 | t0001 | g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MOSPD2_chrX_14868421_14927327 | MOSPD2 |
| a0001c0001t0001g0086 | a0001 | c0001 | t0001 | g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MOSPD2_chrX_14868421_14927327 | MOSPD2 |
| a0001c0001t0001g0087 | a0001 | c0001 | t0001 | g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MOSPD2_chrX_14868421_14927327 | MOSPD2 |
| a0001c0001t0001g0089 | a0001 | c0001 | t0001 | g0089 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MOSPD2_chrX_14868421_14927327 | MOSPD2 |
| a0001c0001t0001g0090 | a0001 | c0001 | t0001 | g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MOSPD2_chrX_14868421_14927327 | MOSPD2 |
| a0001c0001t0001g0091 | a0001 | c0001 | t0001 | g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MOSPD2_chrX_14868421_14927327 | MOSPD2 |
| a0001c0001t0001g0092 | a0001 | c0001 | t0001 | g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MOSPD2_chrX_14868421_14927327 | MOSPD2 |
| a0001c0001t0001g0093 | a0001 | c0001 | t0001 | g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MOSPD2_chrX_14868421_14927327 | MOSPD2 |
| a0001c0001t0001g0094 | a0001 | c0001 | t0001 | g0094 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MOSPD2_chrX_14868421_14927327 | MOSPD2 |
| a0001c0001t0001g0095 | a0001 | c0001 | t0001 | g0095 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MOSPD2_chrX_14868421_14927327 | MOSPD2 |
| a0001c0001t0001g0096 | a0001 | c0001 | t0001 | g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MOSPD2_chrX_14868421_14927327 | MOSPD2 |
| a0001c0001t0001g0097 | a0001 | c0001 | t0001 | g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MOSPD2_chrX_14868421_14927327 | MOSPD2 |
| a0001c0001t0001g0098 | a0001 | c0001 | t0001 | g0098 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MOSPD2_chrX_14868421_14927327 | MOSPD2 |
| a0001c0001t0001g0099 | a0001 | c0001 | t0001 | g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MOSPD2_chrX_14868421_14927327 | MOSPD2 |
| a0001c0001t0001g0100 | a0001 | c0001 | t0001 | g0100 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MOSPD2_chrX_14868421_14927327 | MOSPD2 |
| a0001c0001t0001g0101 | a0001 | c0001 | t0001 | g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MOSPD2_chrX_14868421_14927327 | MOSPD2 |
| a0001c0001t0001g0102 | a0001 | c0001 | t0001 | g0102 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MOSPD2_chrX_14868421_14927327 | MOSPD2 |
| a0001c0001t0001g0103 | a0001 | c0001 | t0001 | g0103 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MOSPD2_chrX_14868421_14927327 | MOSPD2 |
| a0001c0001t0001g0105 | a0001 | c0001 | t0001 | g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MOSPD2_chrX_14868421_14927327 | MOSPD2 |
| a0001c0001t0001g0106 | a0001 | c0001 | t0001 | g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MOSPD2_chrX_14868421_14927327 | MOSPD2 |
| a0001c0001t0001g0107 | a0001 | c0001 | t0001 | g0107 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MOSPD2_chrX_14868421_14927327 | MOSPD2 |
| a0001c0001t0001g0108 | a0001 | c0001 | t0001 | g0108 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MOSPD2_chrX_14868421_14927327 | MOSPD2 |
| a0001c0001t0001g0109 | a0001 | c0001 | t0001 | g0109 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MOSPD2_chrX_14868421_14927327 | MOSPD2 |
| a0001c0001t0001g0110 | a0001 | c0001 | t0001 | g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MOSPD2_chrX_14868421_14927327 | MOSPD2 |
| a0001c0001t0001g0111 | a0001 | c0001 | t0001 | g0111 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MOSPD2_chrX_14868421_14927327 | MOSPD2 |
| a0001c0001t0001g0112 | a0001 | c0001 | t0001 | g0112 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MOSPD2_chrX_14868421_14927327 | MOSPD2 |
| a0001c0001t0001g0113 | a0001 | c0001 | t0001 | g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MOSPD2_chrX_14868421_14927327 | MOSPD2 |
| a0001c0001t0001g0114 | a0001 | c0001 | t0001 | g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MOSPD2_chrX_14868421_14927327 | MOSPD2 |
| a0001c0001t0001g0115 | a0001 | c0001 | t0001 | g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MOSPD2_chrX_14868421_14927327 | MOSPD2 |
| a0001c0001t0001g0116 | a0001 | c0001 | t0001 | g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MOSPD2_chrX_14868421_14927327 | MOSPD2 |
| a0001c0001t0001g0117 | a0001 | c0001 | t0001 | g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MOSPD2_chrX_14868421_14927327 | MOSPD2 |
| a0001c0001t0001g0118 | a0001 | c0001 | t0001 | g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MOSPD2_chrX_14868421_14927327 | MOSPD2 |
| a0001c0001t0001g0119 | a0001 | c0001 | t0001 | g0119 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MOSPD2_chrX_14868421_14927327 | MOSPD2 |
| a0001c0001t0001g0120 | a0001 | c0001 | t0001 | g0120 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MOSPD2_chrX_14868421_14927327 | MOSPD2 |
| a0001c0001t0001g0121 | a0001 | c0001 | t0001 | g0121 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MOSPD2_chrX_14868421_14927327 | MOSPD2 |
| a0001c0001t0001g0122 | a0001 | c0001 | t0001 | g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MOSPD2_chrX_14868421_14927327 | MOSPD2 |
| a0001c0001t0001g0123 | a0001 | c0001 | t0001 | g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MOSPD2_chrX_14868421_14927327 | MOSPD2 |
| a0001c0001t0001g0124 | a0001 | c0001 | t0001 | g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MOSPD2_chrX_14868421_14927327 | MOSPD2 |
| a0001c0001t0001g0125 | a0001 | c0001 | t0001 | g0125 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | MOSPD2_chrX_14868421_14927327 | MOSPD2 |
| a0001c0001t0001g0126 | a0001 | c0001 | t0001 | g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MOSPD2_chrX_14868421_14927327 | MOSPD2 |
| a0001c0001t0001g0127 | a0001 | c0001 | t0001 | g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MOSPD2_chrX_14868421_14927327 | MOSPD2 |
| a0001c0001t0001g0128 | a0001 | c0001 | t0001 | g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MOSPD2_chrX_14868421_14927327 | MOSPD2 |
| a0001c0001t0001g0129 | a0001 | c0001 | t0001 | g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MOSPD2_chrX_14868421_14927327 | MOSPD2 |
| a0001c0001t0001g0130 | a0001 | c0001 | t0001 | g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MOSPD2_chrX_14868421_14927327 | MOSPD2 |
| a0001c0001t0001g0131 | a0001 | c0001 | t0001 | g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MOSPD2_chrX_14868421_14927327 | MOSPD2 |
| a0001c0001t0001g0132 | a0001 | c0001 | t0001 | g0132 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MOSPD2_chrX_14868421_14927327 | MOSPD2 |
| a0001c0001t0001g0133 | a0001 | c0001 | t0001 | g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MOSPD2_chrX_14868421_14927327 | MOSPD2 |
| a0001c0001t0001g0134 | a0001 | c0001 | t0001 | g0134 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MOSPD2_chrX_14868421_14927327 | MOSPD2 |
| a0001c0001t0001g0135 | a0001 | c0001 | t0001 | g0135 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MOSPD2_chrX_14868421_14927327 | MOSPD2 |
| a0001c0001t0001g0138 | a0001 | c0001 | t0001 | g0138 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MOSPD2_chrX_14868421_14927327 | MOSPD2 |
| a0001c0001t0001g0139 | a0001 | c0001 | t0001 | g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MOSPD2_chrX_14868421_14927327 | MOSPD2 |
| a0001c0001t0001g0140 | a0001 | c0001 | t0001 | g0140 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MOSPD2_chrX_14868421_14927327 | MOSPD2 |
| a0001c0001t0001g0141 | a0001 | c0001 | t0001 | g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MOSPD2_chrX_14868421_14927327 | MOSPD2 |
| a0001c0001t0001g0142 | a0001 | c0001 | t0001 | g0142 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MOSPD2_chrX_14868421_14927327 | MOSPD2 |
| a0001c0001t0001g0143 | a0001 | c0001 | t0001 | g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MOSPD2_chrX_14868421_14927327 | MOSPD2 |
| a0001c0001t0001g0144 | a0001 | c0001 | t0001 | g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MOSPD2_chrX_14868421_14927327 | MOSPD2 |
| a0001c0001t0001g0145 | a0001 | c0001 | t0001 | g0145 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MOSPD2_chrX_14868421_14927327 | MOSPD2 |
| a0001c0001t0001g0147 | a0001 | c0001 | t0001 | g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MOSPD2_chrX_14868421_14927327 | MOSPD2 |
| a0001c0001t0001g0148 | a0001 | c0001 | t0001 | g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MOSPD2_chrX_14868421_14927327 | MOSPD2 |
| a0001c0001t0001g0149 | a0001 | c0001 | t0001 | g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MOSPD2_chrX_14868421_14927327 | MOSPD2 |
| a0001c0001t0001g0150 | a0001 | c0001 | t0001 | g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MOSPD2_chrX_14868421_14927327 | MOSPD2 |
| a0001c0001t0001g0151 | a0001 | c0001 | t0001 | g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MOSPD2_chrX_14868421_14927327 | MOSPD2 |
| a0001c0001t0001g0152 | a0001 | c0001 | t0001 | g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MOSPD2_chrX_14868421_14927327 | MOSPD2 |
| a0001c0001t0001g0153 | a0001 | c0001 | t0001 | g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MOSPD2_chrX_14868421_14927327 | MOSPD2 |
| a0001c0001t0001g0154 | a0001 | c0001 | t0001 | g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MOSPD2_chrX_14868421_14927327 | MOSPD2 |
| a0001c0001t0001g0155 | a0001 | c0001 | t0001 | g0155 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MOSPD2_chrX_14868421_14927327 | MOSPD2 |
| a0001c0001t0001g0156 | a0001 | c0001 | t0001 | g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MOSPD2_chrX_14868421_14927327 | MOSPD2 |
| a0001c0001t0001g0157 | a0001 | c0001 | t0001 | g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MOSPD2_chrX_14868421_14927327 | MOSPD2 |
| a0001c0001t0001g0158 | a0001 | c0001 | t0001 | g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MOSPD2_chrX_14868421_14927327 | MOSPD2 |
| a0001c0001t0001g0159 | a0001 | c0001 | t0001 | g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MOSPD2_chrX_14868421_14927327 | MOSPD2 |
| a0001c0001t0001g0160 | a0001 | c0001 | t0001 | g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MOSPD2_chrX_14868421_14927327 | MOSPD2 |
| a0001c0001t0001g0161 | a0001 | c0001 | t0001 | g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MOSPD2_chrX_14868421_14927327 | MOSPD2 |
| a0001c0001t0001g0163 | a0001 | c0001 | t0001 | g0163 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MOSPD2_chrX_14868421_14927327 | MOSPD2 |
| a0001c0001t0001g0164 | a0001 | c0001 | t0001 | g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MOSPD2_chrX_14868421_14927327 | MOSPD2 |
| a0001c0001t0001g0166 | a0001 | c0001 | t0001 | g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MOSPD2_chrX_14868421_14927327 | MOSPD2 |
| a0001c0001t0001g0167 | a0001 | c0001 | t0001 | g0167 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MOSPD2_chrX_14868421_14927327 | MOSPD2 |
| a0001c0001t0001g0168 | a0001 | c0001 | t0001 | g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MOSPD2_chrX_14868421_14927327 | MOSPD2 |
| a0001c0001t0001g0169 | a0001 | c0001 | t0001 | g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MOSPD2_chrX_14868421_14927327 | MOSPD2 |
| a0001c0001t0001g0170 | a0001 | c0001 | t0001 | g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MOSPD2_chrX_14868421_14927327 | MOSPD2 |
| a0001c0001t0001g0171 | a0001 | c0001 | t0001 | g0171 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | MOSPD2_chrX_14868421_14927327 | MOSPD2 |
| a0001c0001t0001g0172 | a0001 | c0001 | t0001 | g0172 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MOSPD2_chrX_14868421_14927327 | MOSPD2 |
| a0001c0001t0001g0173 | a0001 | c0001 | t0001 | g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MOSPD2_chrX_14868421_14927327 | MOSPD2 |
| a0001c0001t0001g0174 | a0001 | c0001 | t0001 | g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MOSPD2_chrX_14868421_14927327 | MOSPD2 |
| a0001c0001t0001g0175 | a0001 | c0001 | t0001 | g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MOSPD2_chrX_14868421_14927327 | MOSPD2 |
| a0001c0001t0001g0176 | a0001 | c0001 | t0001 | g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MOSPD2_chrX_14868421_14927327 | MOSPD2 |
| a0001c0001t0001g0177 | a0001 | c0001 | t0001 | g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MOSPD2_chrX_14868421_14927327 | MOSPD2 |
| a0001c0001t0001g0178 | a0001 | c0001 | t0001 | g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MOSPD2_chrX_14868421_14927327 | MOSPD2 |
| a0001c0001t0001g0179 | a0001 | c0001 | t0001 | g0179 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MOSPD2_chrX_14868421_14927327 | MOSPD2 |
| a0001c0001t0001g0180 | a0001 | c0001 | t0001 | g0180 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MOSPD2_chrX_14868421_14927327 | MOSPD2 |
| a0001c0001t0001g0181 | a0001 | c0001 | t0001 | g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MOSPD2_chrX_14868421_14927327 | MOSPD2 |
| a0001c0001t0001g0182 | a0001 | c0001 | t0001 | g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MOSPD2_chrX_14868421_14927327 | MOSPD2 |
| a0001c0001t0001g0183 | a0001 | c0001 | t0001 | g0183 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MOSPD2_chrX_14868421_14927327 | MOSPD2 |
| a0001c0001t0001g0187 | a0001 | c0001 | t0001 | g0187 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MOSPD2_chrX_14868421_14927327 | MOSPD2 |
| a0001c0001t0001g0188 | a0001 | c0001 | t0001 | g0188 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MOSPD2_chrX_14868421_14927327 | MOSPD2 |
| a0001c0001t0001g0189 | a0001 | c0001 | t0001 | g0189 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MOSPD2_chrX_14868421_14927327 | MOSPD2 |
| a0001c0001t0001g0190 | a0001 | c0001 | t0001 | g0190 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MOSPD2_chrX_14868421_14927327 | MOSPD2 |
| a0001c0001t0001g0191 | a0001 | c0001 | t0001 | g0191 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MOSPD2_chrX_14868421_14927327 | MOSPD2 |
| a0001c0001t0001g0192 | a0001 | c0001 | t0001 | g0192 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MOSPD2_chrX_14868421_14927327 | MOSPD2 |
| a0001c0001t0001g0193 | a0001 | c0001 | t0001 | g0193 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MOSPD2_chrX_14868421_14927327 | MOSPD2 |
| a0001c0001t0001g0194 | a0001 | c0001 | t0001 | g0194 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MOSPD2_chrX_14868421_14927327 | MOSPD2 |
| a0001c0001t0001g0195 | a0001 | c0001 | t0001 | g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MOSPD2_chrX_14868421_14927327 | MOSPD2 |
| a0001c0001t0001g0196 | a0001 | c0001 | t0001 | g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MOSPD2_chrX_14868421_14927327 | MOSPD2 |
| a0001c0001t0001g0197 | a0001 | c0001 | t0001 | g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MOSPD2_chrX_14868421_14927327 | MOSPD2 |
| a0001c0001t0001g0199 | a0001 | c0001 | t0001 | g0199 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MOSPD2_chrX_14868421_14927327 | MOSPD2 |
| a0001c0001t0001g0205 | a0001 | c0001 | t0001 | g0205 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MOSPD2_chrX_14868421_14927327 | MOSPD2 |
| a0001c0001t0001g0206 | a0001 | c0001 | t0001 | g0206 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MOSPD2_chrX_14868421_14927327 | MOSPD2 |
| a0001c0001t0002g0003 | a0001 | c0001 | t0002 | g0003 | 0/0 | 4 | 3 | 1 | 0 | 0 | 0 | MOSPD2_chrX_14868421_14927327 | MOSPD2 |
| a0001c0001t0002g0006 | a0001 | c0001 | t0002 | g0006 | 0/0 | 3 | 2 | 1 | 0 | 0 | 0 | MOSPD2_chrX_14868421_14927327 | MOSPD2 |
| a0001c0001t0002g0011 | a0001 | c0001 | t0002 | g0011 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MOSPD2_chrX_14868421_14927327 | MOSPD2 |
| a0001c0001t0002g0012 | a0001 | c0001 | t0002 | g0012 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MOSPD2_chrX_14868421_14927327 | MOSPD2 |
| a0001c0001t0002g0031 | a0001 | c0001 | t0002 | g0031 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MOSPD2_chrX_14868421_14927327 | MOSPD2 |
| a0001c0001t0002g0039 | a0001 | c0001 | t0002 | g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MOSPD2_chrX_14868421_14927327 | MOSPD2 |
| a0001c0001t0002g0040 | a0001 | c0001 | t0002 | g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MOSPD2_chrX_14868421_14927327 | MOSPD2 |
| a0001c0001t0002g0203 | a0001 | c0001 | t0002 | g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MOSPD2_chrX_14868421_14927327 | MOSPD2 |
| a0001c0001t0002g0204 | a0001 | c0001 | t0002 | g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MOSPD2_chrX_14868421_14927327 | MOSPD2 |
| a0001c0001t0003g0005 | a0001 | c0001 | t0003 | g0005 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | MOSPD2_chrX_14868421_14927327 | MOSPD2 |
| a0001c0001t0003g0007 | a0001 | c0001 | t0003 | g0007 | 0/0 | 3 | 2 | 1 | 0 | 0 | 0 | MOSPD2_chrX_14868421_14927327 | MOSPD2 |
| a0001c0001t0003g0026 | a0001 | c0001 | t0003 | g0026 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MOSPD2_chrX_14868421_14927327 | MOSPD2 |
| a0001c0001t0003g0041 | a0001 | c0001 | t0003 | g0041 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MOSPD2_chrX_14868421_14927327 | MOSPD2 |
| a0001c0001t0003g0184 | a0001 | c0001 | t0003 | g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MOSPD2_chrX_14868421_14927327 | MOSPD2 |
| a0001c0001t0003g0185 | a0001 | c0001 | t0003 | g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MOSPD2_chrX_14868421_14927327 | MOSPD2 |
| a0001c0001t0003g0186 | a0001 | c0001 | t0003 | g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MOSPD2_chrX_14868421_14927327 | MOSPD2 |
| a0001c0001t0003g0198 | a0001 | c0001 | t0003 | g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MOSPD2_chrX_14868421_14927327 | MOSPD2 |
| a0001c0001t0004g0200 | a0001 | c0001 | t0004 | g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MOSPD2_chrX_14868421_14927327 | MOSPD2 |
| a0001c0001t0004g0201 | a0001 | c0001 | t0004 | g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MOSPD2_chrX_14868421_14927327 | MOSPD2 |
| a0001c0001t0004g0202 | a0001 | c0001 | t0004 | g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MOSPD2_chrX_14868421_14927327 | MOSPD2 |
| a0001c0001t0005g0018 | a0001 | c0001 | t0005 | g0018 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | MOSPD2_chrX_14868421_14927327 | MOSPD2 |
| a0001c0001t0006g0014 | a0001 | c0001 | t0006 | g0014 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MOSPD2_chrX_14868421_14927327 | MOSPD2 |
| a0001c0001t0007g0033 | a0001 | c0001 | t0007 | g0033 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MOSPD2_chrX_14868421_14927327 | MOSPD2 |
| a0001c0001t0008g0162 | a0001 | c0001 | t0008 | g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MOSPD2_chrX_14868421_14927327 | MOSPD2 |
| a0001c0001t0009g0146 | a0001 | c0001 | t0009 | g0146 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MOSPD2_chrX_14868421_14927327 | MOSPD2 |
| a0001c0001t0010g0104 | a0001 | c0001 | t0010 | g0104 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MOSPD2_chrX_14868421_14927327 | MOSPD2 |
| a0001c0001t0011g0136 | a0001 | c0001 | t0011 | g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MOSPD2_chrX_14868421_14927327 | MOSPD2 |
| a0001c0001t0012g0088 | a0001 | c0001 | t0012 | g0088 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MOSPD2_chrX_14868421_14927327 | MOSPD2 |
| a0001c0003t0001g0023 | a0001 | c0003 | t0001 | g0023 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | MOSPD2_chrX_14868421_14927327 | MOSPD2 |
| a0001c0003t0001g0137 | a0001 | c0003 | t0001 | g0137 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MOSPD2_chrX_14868421_14927327 | MOSPD2 |
| a0001c0004t0001g0165 | a0001 | c0004 | t0001 | g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MOSPD2_chrX_14868421_14927327 | MOSPD2 |
| a0002c0002t0001g0034 | a0002 | c0002 | t0001 | g0034 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MOSPD2_chrX_14868421_14927327 | MOSPD2 |
| a0002c0002t0001g0035 | a0002 | c0002 | t0001 | g0035 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MOSPD2_chrX_14868421_14927327 | MOSPD2 |
| a0002c0002t0001g0036 | a0002 | c0002 | t0001 | g0036 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MOSPD2_chrX_14868421_14927327 | MOSPD2 |
| a0002c0002t0001g0037 | a0002 | c0002 | t0001 | g0037 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MOSPD2_chrX_14868421_14927327 | MOSPD2 |
| sampleid | haplotypeid | ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename |
|---|---|---|---|---|---|---|---|---|---|
| HG00140 | hp1 | a0001 | c0001 | t0001 | g0024 | EUR | GBR | MOSPD2_chrX_14868421_14927327 | MOSPD2 |
| HG00280 | hp1 | a0002 | c0002 | t0001 | g0035 | EUR | FIN | MOSPD2_chrX_14868421_14927327 | MOSPD2 |
| HG00408 | hp1 | a0001 | c0001 | t0001 | g0106 | EAS | CHS | MOSPD2_chrX_14868421_14927327 | MOSPD2 |
| HG00408 | hp2 | a0001 | c0001 | t0001 | g0152 | EAS | CHS | MOSPD2_chrX_14868421_14927327 | MOSPD2 |
| HG00423 | hp1 | a0001 | c0001 | t0001 | g0016 | EAS | CHS | MOSPD2_chrX_14868421_14927327 | MOSPD2 |
| HG00423 | hp2 | a0001 | c0001 | t0001 | g0159 | EAS | CHS | MOSPD2_chrX_14868421_14927327 | MOSPD2 |
| HG00558 | hp1 | a0001 | c0001 | t0001 | g0013 | EAS | CHS | MOSPD2_chrX_14868421_14927327 | MOSPD2 |
| HG00558 | hp2 | a0001 | c0001 | t0001 | g0175 | EAS | CHS | MOSPD2_chrX_14868421_14927327 | MOSPD2 |
| HG00609 | hp1 | a0001 | c0001 | t0001 | g0178 | EAS | CHS | MOSPD2_chrX_14868421_14927327 | MOSPD2 |
| HG00621 | hp1 | a0001 | c0001 | t0001 | g0056 | EAS | CHS | MOSPD2_chrX_14868421_14927327 | MOSPD2 |
| HG00639 | hp1 | a0001 | c0001 | t0001 | g0187 | AMR | PUR | MOSPD2_chrX_14868421_14927327 | MOSPD2 |
| HG00639 | hp2 | a0001 | c0001 | t0001 | g0111 | AMR | PUR | MOSPD2_chrX_14868421_14927327 | MOSPD2 |
| HG00642 | hp1 | a0001 | c0001 | t0001 | g0205 | AMR | PUR | MOSPD2_chrX_14868421_14927327 | MOSPD2 |
| HG00673 | hp1 | a0001 | c0001 | t0001 | g0069 | EAS | CHS | MOSPD2_chrX_14868421_14927327 | MOSPD2 |
| HG00733 | hp1 | a0001 | c0001 | t0001 | g0193 | AMR | PUR | MOSPD2_chrX_14868421_14927327 | MOSPD2 |
| HG00733 | hp2 | a0001 | c0001 | t0001 | g0183 | AMR | PUR | MOSPD2_chrX_14868421_14927327 | MOSPD2 |
| HG00735 | hp1 | a0001 | c0001 | t0001 | g0192 | AMR | PUR | MOSPD2_chrX_14868421_14927327 | MOSPD2 |
| HG00735 | hp2 | a0001 | c0001 | t0001 | g0107 | AMR | PUR | MOSPD2_chrX_14868421_14927327 | MOSPD2 |
| HG00738 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | MOSPD2_chrX_14868421_14927327 | MOSPD2 |
| HG00741 | hp1 | a0001 | c0001 | t0001 | g0142 | AMR | PUR | MOSPD2_chrX_14868421_14927327 | MOSPD2 |
| HG00741 | hp2 | a0001 | c0001 | t0001 | g0019 | AMR | PUR | MOSPD2_chrX_14868421_14927327 | MOSPD2 |
| HG01069 | hp1 | a0001 | c0001 | t0001 | g0025 | AMR | PUR | MOSPD2_chrX_14868421_14927327 | MOSPD2 |
| HG01070 | hp1 | a0001 | c0001 | t0001 | g0155 | AMR | PUR | MOSPD2_chrX_14868421_14927327 | MOSPD2 |
| HG01070 | hp2 | a0001 | c0001 | t0001 | g0020 | AMR | PUR | MOSPD2_chrX_14868421_14927327 | MOSPD2 |
| HG01071 | hp1 | a0001 | c0001 | t0001 | g0020 | AMR | PUR | MOSPD2_chrX_14868421_14927327 | MOSPD2 |
| HG01071 | hp2 | a0001 | c0001 | t0001 | g0025 | AMR | PUR | MOSPD2_chrX_14868421_14927327 | MOSPD2 |
| HG01074 | hp1 | a0001 | c0001 | t0003 | g0041 | AMR | PUR | MOSPD2_chrX_14868421_14927327 | MOSPD2 |
| HG01081 | hp1 | a0001 | c0001 | t0001 | g0188 | AMR | PUR | MOSPD2_chrX_14868421_14927327 | MOSPD2 |
| HG01081 | hp2 | a0001 | c0001 | t0001 | g0014 | AMR | PUR | MOSPD2_chrX_14868421_14927327 | MOSPD2 |
| HG01099 | hp1 | a0001 | c0001 | t0006 | g0014 | AMR | PUR | MOSPD2_chrX_14868421_14927327 | MOSPD2 |
| HG01106 | hp1 | a0001 | c0001 | t0002 | g0003 | AMR | PUR | MOSPD2_chrX_14868421_14927327 | MOSPD2 |
| HG01109 | hp1 | a0001 | c0001 | t0001 | g0199 | AMR | PUR | MOSPD2_chrX_14868421_14927327 | MOSPD2 |
| HG01167 | hp1 | a0001 | c0001 | t0005 | g0018 | AMR | PUR | MOSPD2_chrX_14868421_14927327 | MOSPD2 |
| HG01168 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | MOSPD2_chrX_14868421_14927327 | MOSPD2 |
| HG01168 | hp2 | a0001 | c0003 | t0001 | g0023 | AMR | PUR | MOSPD2_chrX_14868421_14927327 | MOSPD2 |
| HG01169 | hp1 | a0001 | c0001 | t0005 | g0018 | AMR | PUR | MOSPD2_chrX_14868421_14927327 | MOSPD2 |
| HG01169 | hp2 | a0001 | c0003 | t0001 | g0023 | AMR | PUR | MOSPD2_chrX_14868421_14927327 | MOSPD2 |
| HG01175 | hp1 | a0001 | c0003 | t0001 | g0137 | AMR | PUR | MOSPD2_chrX_14868421_14927327 | MOSPD2 |
| HG01175 | hp2 | a0001 | c0001 | t0010 | g0104 | AMR | PUR | MOSPD2_chrX_14868421_14927327 | MOSPD2 |
| HG01192 | hp1 | a0001 | c0001 | t0012 | g0088 | AMR | PUR | MOSPD2_chrX_14868421_14927327 | MOSPD2 |
| HG01243 | hp1 | a0001 | c0001 | t0002 | g0006 | AMR | PUR | MOSPD2_chrX_14868421_14927327 | MOSPD2 |
| HG01255 | hp1 | a0001 | c0001 | t0001 | g0112 | AMR | CLM | MOSPD2_chrX_14868421_14927327 | MOSPD2 |
| HG01256 | hp1 | a0001 | c0001 | t0009 | g0146 | AMR | CLM | MOSPD2_chrX_14868421_14927327 | MOSPD2 |
| HG01257 | hp1 | a0001 | c0001 | t0001 | g0108 | AMR | CLM | MOSPD2_chrX_14868421_14927327 | MOSPD2 |
| HG01257 | hp2 | a0001 | c0001 | t0001 | g0027 | AMR | CLM | MOSPD2_chrX_14868421_14927327 | MOSPD2 |
| HG01258 | hp1 | a0001 | c0001 | t0001 | g0027 | AMR | CLM | MOSPD2_chrX_14868421_14927327 | MOSPD2 |
| HG01261 | hp1 | a0002 | c0002 | t0001 | g0037 | AMR | CLM | MOSPD2_chrX_14868421_14927327 | MOSPD2 |
| HG01358 | hp1 | a0001 | c0001 | t0001 | g0180 | AMR | CLM | MOSPD2_chrX_14868421_14927327 | MOSPD2 |
| HG01361 | hp1 | a0001 | c0001 | t0001 | g0132 | AMR | CLM | MOSPD2_chrX_14868421_14927327 | MOSPD2 |
| HG01361 | hp2 | a0001 | c0001 | t0001 | g0120 | AMR | CLM | MOSPD2_chrX_14868421_14927327 | MOSPD2 |
| HG01433 | hp1 | a0001 | c0001 | t0001 | g0163 | AMR | CLM | MOSPD2_chrX_14868421_14927327 | MOSPD2 |
| HG01496 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | MOSPD2_chrX_14868421_14927327 | MOSPD2 |
| HG01496 | hp2 | a0001 | c0001 | t0001 | g0191 | AMR | CLM | MOSPD2_chrX_14868421_14927327 | MOSPD2 |
| HG01515 | hp1 | a0001 | c0001 | t0001 | g0206 | EUR | IBS | MOSPD2_chrX_14868421_14927327 | MOSPD2 |
| HG01516 | hp1 | a0001 | c0001 | t0001 | g0190 | EUR | IBS | MOSPD2_chrX_14868421_14927327 | MOSPD2 |
| HG01516 | hp2 | a0002 | c0002 | t0001 | g0036 | EUR | IBS | MOSPD2_chrX_14868421_14927327 | MOSPD2 |
| HG01884 | hp1 | a0001 | c0001 | t0003 | g0186 | AFR | ACB | MOSPD2_chrX_14868421_14927327 | MOSPD2 |
| HG01884 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | ACB | MOSPD2_chrX_14868421_14927327 | MOSPD2 |
| HG01891 | hp1 | a0001 | c0001 | t0002 | g0012 | AFR | ACB | MOSPD2_chrX_14868421_14927327 | MOSPD2 |
| HG01891 | hp2 | a0001 | c0001 | t0011 | g0136 | AFR | ACB | MOSPD2_chrX_14868421_14927327 | MOSPD2 |
| HG01928 | hp1 | a0001 | c0001 | t0001 | g0134 | AMR | PEL | MOSPD2_chrX_14868421_14927327 | MOSPD2 |
| HG01934 | hp1 | a0001 | c0001 | t0001 | g0049 | AMR | PEL | MOSPD2_chrX_14868421_14927327 | MOSPD2 |
| HG01943 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | MOSPD2_chrX_14868421_14927327 | MOSPD2 |
| HG01952 | hp1 | a0001 | c0001 | t0001 | g0145 | AMR | PEL | MOSPD2_chrX_14868421_14927327 | MOSPD2 |
| HG01975 | hp1 | a0001 | c0001 | t0001 | g0010 | AMR | PEL | MOSPD2_chrX_14868421_14927327 | MOSPD2 |
| HG01975 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | PEL | MOSPD2_chrX_14868421_14927327 | MOSPD2 |
| HG01981 | hp1 | a0001 | c0001 | t0001 | g0179 | AMR | PEL | MOSPD2_chrX_14868421_14927327 | MOSPD2 |
| HG01981 | hp2 | a0001 | c0001 | t0001 | g0076 | AMR | PEL | MOSPD2_chrX_14868421_14927327 | MOSPD2 |
| HG02015 | hp1 | a0001 | c0001 | t0001 | g0143 | EAS | KHV | MOSPD2_chrX_14868421_14927327 | MOSPD2 |
| HG02027 | hp1 | a0001 | c0001 | t0001 | g0096 | EAS | KHV | MOSPD2_chrX_14868421_14927327 | MOSPD2 |
| HG02040 | hp1 | a0001 | c0001 | t0001 | g0055 | EAS | KHV | MOSPD2_chrX_14868421_14927327 | MOSPD2 |
| HG02055 | hp1 | a0001 | c0001 | t0001 | g0118 | AFR | ACB | MOSPD2_chrX_14868421_14927327 | MOSPD2 |
| HG02056 | hp1 | a0001 | c0001 | t0001 | g0161 | EAS | KHV | MOSPD2_chrX_14868421_14927327 | MOSPD2 |
| HG02071 | hp1 | a0001 | c0001 | t0001 | g0015 | EAS | KHV | MOSPD2_chrX_14868421_14927327 | MOSPD2 |
| HG02074 | hp1 | a0001 | c0001 | t0001 | g0084 | EAS | KHV | MOSPD2_chrX_14868421_14927327 | MOSPD2 |
| HG02080 | hp1 | a0001 | c0001 | t0001 | g0091 | EAS | KHV | MOSPD2_chrX_14868421_14927327 | MOSPD2 |
| HG02080 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | KHV | MOSPD2_chrX_14868421_14927327 | MOSPD2 |
| HG02083 | hp1 | a0001 | c0001 | t0001 | g0015 | EAS | KHV | MOSPD2_chrX_14868421_14927327 | MOSPD2 |
| HG02129 | hp1 | a0001 | c0001 | t0001 | g0101 | EAS | KHV | MOSPD2_chrX_14868421_14927327 | MOSPD2 |
| HG02132 | hp1 | a0001 | c0001 | t0001 | g0077 | EAS | KHV | MOSPD2_chrX_14868421_14927327 | MOSPD2 |
| HG02135 | hp1 | a0001 | c0001 | t0001 | g0110 | EAS | KHV | MOSPD2_chrX_14868421_14927327 | MOSPD2 |
| HG02145 | hp1 | a0001 | c0001 | t0003 | g0185 | AFR | ACB | MOSPD2_chrX_14868421_14927327 | MOSPD2 |
| HG02148 | hp1 | a0001 | c0001 | t0001 | g0052 | AMR | PEL | MOSPD2_chrX_14868421_14927327 | MOSPD2 |
| HG02148 | hp2 | a0001 | c0001 | t0001 | g0103 | AMR | PEL | MOSPD2_chrX_14868421_14927327 | MOSPD2 |
| HG02257 | hp1 | a0001 | c0001 | t0001 | g0021 | AFR | ACB | MOSPD2_chrX_14868421_14927327 | MOSPD2 |
| HG02257 | hp2 | a0001 | c0001 | t0001 | g0032 | AFR | ACB | MOSPD2_chrX_14868421_14927327 | MOSPD2 |
| HG02258 | hp1 | a0001 | c0001 | t0003 | g0198 | AFR | ACB | MOSPD2_chrX_14868421_14927327 | MOSPD2 |
| HG02280 | hp1 | a0001 | c0001 | t0002 | g0006 | AFR | ACB | MOSPD2_chrX_14868421_14927327 | MOSPD2 |
| HG02280 | hp2 | a0001 | c0001 | t0002 | g0003 | AFR | ACB | MOSPD2_chrX_14868421_14927327 | MOSPD2 |
| HG02293 | hp1 | a0001 | c0001 | t0003 | g0007 | AMR | PEL | MOSPD2_chrX_14868421_14927327 | MOSPD2 |
| HG02293 | hp2 | a0001 | c0001 | t0001 | g0189 | AMR | PEL | MOSPD2_chrX_14868421_14927327 | MOSPD2 |
| HG02451 | hp1 | a0001 | c0001 | t0002 | g0204 | AFR | ACB | MOSPD2_chrX_14868421_14927327 | MOSPD2 |
| HG02451 | hp2 | a0001 | c0001 | t0001 | g0149 | AFR | ACB | MOSPD2_chrX_14868421_14927327 | MOSPD2 |
| HG02523 | hp1 | a0001 | c0001 | t0001 | g0047 | EAS | KHV | MOSPD2_chrX_14868421_14927327 | MOSPD2 |
| HG02523 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | MOSPD2_chrX_14868421_14927327 | MOSPD2 |
| HG02572 | hp1 | a0001 | c0001 | t0003 | g0005 | AFR | GWD | MOSPD2_chrX_14868421_14927327 | MOSPD2 |
| HG02602 | hp1 | a0001 | c0001 | t0001 | g0067 | SAS | PJL | MOSPD2_chrX_14868421_14927327 | MOSPD2 |
| HG02615 | hp1 | a0001 | c0001 | t0001 | g0133 | AFR | GWD | MOSPD2_chrX_14868421_14927327 | MOSPD2 |
| HG02615 | hp2 | a0001 | c0001 | t0001 | g0141 | AFR | GWD | MOSPD2_chrX_14868421_14927327 | MOSPD2 |
| HG02622 | hp1 | a0001 | c0001 | t0003 | g0007 | AFR | GWD | MOSPD2_chrX_14868421_14927327 | MOSPD2 |
| HG02622 | hp2 | a0001 | c0001 | t0002 | g0039 | AFR | GWD | MOSPD2_chrX_14868421_14927327 | MOSPD2 |
| HG02630 | hp1 | a0001 | c0004 | t0001 | g0165 | AFR | GWD | MOSPD2_chrX_14868421_14927327 | MOSPD2 |
| HG02630 | hp2 | a0001 | c0001 | t0001 | g0029 | AFR | GWD | MOSPD2_chrX_14868421_14927327 | MOSPD2 |
| HG02647 | hp1 | a0001 | c0001 | t0003 | g0005 | AFR | GWD | MOSPD2_chrX_14868421_14927327 | MOSPD2 |
| HG02698 | hp1 | a0001 | c0001 | t0001 | g0100 | SAS | PJL | MOSPD2_chrX_14868421_14927327 | MOSPD2 |
| HG02717 | hp1 | a0001 | c0001 | t0001 | g0030 | AFR | GWD | MOSPD2_chrX_14868421_14927327 | MOSPD2 |
| HG02723 | hp1 | a0001 | c0001 | t0001 | g0166 | AFR | GWD | MOSPD2_chrX_14868421_14927327 | MOSPD2 |
| HG02723 | hp2 | a0001 | c0001 | t0001 | g0038 | AFR | GWD | MOSPD2_chrX_14868421_14927327 | MOSPD2 |
| HG02735 | hp1 | a0002 | c0002 | t0001 | g0034 | SAS | PJL | MOSPD2_chrX_14868421_14927327 | MOSPD2 |
| HG02738 | hp1 | a0001 | c0001 | t0001 | g0094 | SAS | PJL | MOSPD2_chrX_14868421_14927327 | MOSPD2 |
| HG02809 | hp1 | a0001 | c0001 | t0004 | g0200 | AFR | GWD | MOSPD2_chrX_14868421_14927327 | MOSPD2 |
| HG02809 | hp2 | a0001 | c0001 | t0001 | g0029 | AFR | GWD | MOSPD2_chrX_14868421_14927327 | MOSPD2 |
| HG02818 | hp1 | a0001 | c0001 | t0001 | g0148 | AFR | GWD | MOSPD2_chrX_14868421_14927327 | MOSPD2 |
| HG02818 | hp2 | a0001 | c0001 | t0002 | g0006 | AFR | GWD | MOSPD2_chrX_14868421_14927327 | MOSPD2 |
| HG02886 | hp1 | a0001 | c0001 | t0001 | g0164 | AFR | GWD | MOSPD2_chrX_14868421_14927327 | MOSPD2 |
| HG02886 | hp2 | a0001 | c0001 | t0001 | g0147 | AFR | GWD | MOSPD2_chrX_14868421_14927327 | MOSPD2 |
| HG02895 | hp1 | a0001 | c0001 | t0001 | g0028 | AFR | GWD | MOSPD2_chrX_14868421_14927327 | MOSPD2 |
| HG02897 | hp1 | a0001 | c0001 | t0001 | g0028 | AFR | GWD | MOSPD2_chrX_14868421_14927327 | MOSPD2 |
| HG02897 | hp2 | a0001 | c0001 | t0003 | g0007 | AFR | GWD | MOSPD2_chrX_14868421_14927327 | MOSPD2 |
| HG02922 | hp1 | a0001 | c0001 | t0004 | g0201 | AFR | ESN | MOSPD2_chrX_14868421_14927327 | MOSPD2 |
| HG02922 | hp2 | a0001 | c0001 | t0003 | g0005 | AFR | ESN | MOSPD2_chrX_14868421_14927327 | MOSPD2 |
| HG02965 | hp1 | a0001 | c0001 | t0001 | g0182 | AFR | ESN | MOSPD2_chrX_14868421_14927327 | MOSPD2 |
| HG02970 | hp1 | a0001 | c0001 | t0001 | g0156 | AFR | ESN | MOSPD2_chrX_14868421_14927327 | MOSPD2 |
| HG02970 | hp2 | a0001 | c0001 | t0002 | g0011 | AFR | ESN | MOSPD2_chrX_14868421_14927327 | MOSPD2 |
| HG02976 | hp1 | a0001 | c0001 | t0001 | g0127 | AFR | ESN | MOSPD2_chrX_14868421_14927327 | MOSPD2 |
| HG02976 | hp2 | a0001 | c0001 | t0002 | g0003 | AFR | ESN | MOSPD2_chrX_14868421_14927327 | MOSPD2 |
| HG03017 | hp1 | a0001 | c0001 | t0001 | g0167 | SAS | PJL | MOSPD2_chrX_14868421_14927327 | MOSPD2 |
| HG03041 | hp1 | a0001 | c0001 | t0001 | g0197 | AFR | GWD | MOSPD2_chrX_14868421_14927327 | MOSPD2 |
| HG03041 | hp2 | a0001 | c0001 | t0004 | g0202 | AFR | GWD | MOSPD2_chrX_14868421_14927327 | MOSPD2 |
| HG03098 | hp1 | a0001 | c0001 | t0003 | g0184 | AFR | MSL | MOSPD2_chrX_14868421_14927327 | MOSPD2 |
| HG03130 | hp1 | a0001 | c0001 | t0003 | g0026 | AFR | ESN | MOSPD2_chrX_14868421_14927327 | MOSPD2 |
| HG03139 | hp1 | a0001 | c0001 | t0001 | g0044 | AFR | ESN | MOSPD2_chrX_14868421_14927327 | MOSPD2 |
| HG03195 | hp1 | a0001 | c0001 | t0001 | g0022 | AFR | ESN | MOSPD2_chrX_14868421_14927327 | MOSPD2 |
| HG03195 | hp2 | a0001 | c0001 | t0001 | g0154 | AFR | ESN | MOSPD2_chrX_14868421_14927327 | MOSPD2 |
| HG03209 | hp1 | a0001 | c0001 | t0001 | g0157 | AFR | MSL | MOSPD2_chrX_14868421_14927327 | MOSPD2 |
| HG03225 | hp1 | a0001 | c0001 | t0003 | g0026 | AFR | MSL | MOSPD2_chrX_14868421_14927327 | MOSPD2 |
| HG03239 | hp1 | a0001 | c0001 | t0001 | g0081 | SAS | PJL | MOSPD2_chrX_14868421_14927327 | MOSPD2 |
| HG03239 | hp2 | a0001 | c0001 | t0001 | g0109 | SAS | PJL | MOSPD2_chrX_14868421_14927327 | MOSPD2 |
| HG03453 | hp1 | a0001 | c0001 | t0001 | g0058 | AFR | MSL | MOSPD2_chrX_14868421_14927327 | MOSPD2 |
| HG03453 | hp2 | a0001 | c0001 | t0001 | g0181 | AFR | MSL | MOSPD2_chrX_14868421_14927327 | MOSPD2 |
| HG03486 | hp1 | a0001 | c0001 | t0002 | g0040 | AFR | MSL | MOSPD2_chrX_14868421_14927327 | MOSPD2 |
| HG03486 | hp2 | a0001 | c0001 | t0001 | g0128 | AFR | MSL | MOSPD2_chrX_14868421_14927327 | MOSPD2 |
| HG03490 | hp1 | a0001 | c0001 | t0001 | g0095 | SAS | PJL | MOSPD2_chrX_14868421_14927327 | MOSPD2 |
| HG03492 | hp1 | a0001 | c0001 | t0001 | g0089 | SAS | PJL | MOSPD2_chrX_14868421_14927327 | MOSPD2 |
| HG03516 | hp1 | a0001 | c0001 | t0002 | g0012 | AFR | ESN | MOSPD2_chrX_14868421_14927327 | MOSPD2 |
| HG03516 | hp2 | a0001 | c0001 | t0001 | g0045 | AFR | ESN | MOSPD2_chrX_14868421_14927327 | MOSPD2 |
| HG03540 | hp1 | a0001 | c0001 | t0001 | g0046 | AFR | GWD | MOSPD2_chrX_14868421_14927327 | MOSPD2 |
| HG03540 | hp2 | a0001 | c0001 | t0002 | g0003 | AFR | GWD | MOSPD2_chrX_14868421_14927327 | MOSPD2 |
| HG03579 | hp1 | a0001 | c0001 | t0001 | g0021 | AFR | MSL | MOSPD2_chrX_14868421_14927327 | MOSPD2 |
| HG03654 | hp1 | a0001 | c0001 | t0001 | g0075 | SAS | PJL | MOSPD2_chrX_14868421_14927327 | MOSPD2 |
| HG03669 | hp1 | a0001 | c0001 | t0001 | g0119 | SAS | PJL | MOSPD2_chrX_14868421_14927327 | MOSPD2 |
| HG03669 | hp2 | a0001 | c0001 | t0007 | g0033 | SAS | PJL | MOSPD2_chrX_14868421_14927327 | MOSPD2 |
| HG03688 | hp1 | a0001 | c0001 | t0001 | g0138 | SAS | STU | MOSPD2_chrX_14868421_14927327 | MOSPD2 |
| HG03710 | hp1 | a0001 | c0001 | t0001 | g0102 | SAS | PJL | MOSPD2_chrX_14868421_14927327 | MOSPD2 |
| HG03834 | hp1 | a0001 | c0001 | t0001 | g0135 | SAS | BEB | MOSPD2_chrX_14868421_14927327 | MOSPD2 |
| HG03834 | hp2 | a0001 | c0001 | t0001 | g0068 | SAS | BEB | MOSPD2_chrX_14868421_14927327 | MOSPD2 |
| HG03942 | hp1 | a0001 | c0001 | t0001 | g0194 | SAS | BEB | MOSPD2_chrX_14868421_14927327 | MOSPD2 |
| HG04115 | hp1 | a0001 | c0001 | t0001 | g0121 | SAS | STU | MOSPD2_chrX_14868421_14927327 | MOSPD2 |
| HG04184 | hp1 | a0001 | c0001 | t0001 | g0172 | SAS | BEB | MOSPD2_chrX_14868421_14927327 | MOSPD2 |
| HG04184 | hp2 | a0001 | c0001 | t0001 | g0098 | SAS | BEB | MOSPD2_chrX_14868421_14927327 | MOSPD2 |
| HG04199 | hp1 | a0001 | c0001 | t0001 | g0140 | SAS | STU | MOSPD2_chrX_14868421_14927327 | MOSPD2 |
| HG04204 | hp1 | a0001 | c0001 | t0001 | g0002 | SAS | STU | MOSPD2_chrX_14868421_14927327 | MOSPD2 |
| HG04228 | hp1 | a0001 | c0001 | t0001 | g0074 | SAS | STU | MOSPD2_chrX_14868421_14927327 | MOSPD2 |
| NA18522 | hp1 | a0001 | c0001 | t0001 | g0195 | AFR | YRI | MOSPD2_chrX_14868421_14927327 | MOSPD2 |
| NA18612 | hp1 | a0001 | c0001 | t0001 | g0062 | EAS | CHB | MOSPD2_chrX_14868421_14927327 | MOSPD2 |
| NA18747 | hp1 | a0001 | c0001 | t0001 | g0160 | EAS | CHB | MOSPD2_chrX_14868421_14927327 | MOSPD2 |
| NA18906 | hp1 | a0001 | c0001 | t0001 | g0022 | AFR | YRI | MOSPD2_chrX_14868421_14927327 | MOSPD2 |
| NA18906 | hp2 | a0001 | c0001 | t0003 | g0005 | AFR | YRI | MOSPD2_chrX_14868421_14927327 | MOSPD2 |
| NA18940 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | MOSPD2_chrX_14868421_14927327 | MOSPD2 |
| NA18942 | hp1 | a0001 | c0001 | t0001 | g0090 | EAS | JPT | MOSPD2_chrX_14868421_14927327 | MOSPD2 |
| NA18942 | hp2 | a0001 | c0001 | t0001 | g0115 | EAS | JPT | MOSPD2_chrX_14868421_14927327 | MOSPD2 |
| NA18943 | hp1 | a0001 | c0001 | t0001 | g0114 | EAS | JPT | MOSPD2_chrX_14868421_14927327 | MOSPD2 |
| NA18944 | hp1 | a0001 | c0001 | t0001 | g0092 | EAS | JPT | MOSPD2_chrX_14868421_14927327 | MOSPD2 |
| NA18945 | hp1 | a0001 | c0001 | t0001 | g0170 | EAS | JPT | MOSPD2_chrX_14868421_14927327 | MOSPD2 |
| NA18946 | hp1 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | MOSPD2_chrX_14868421_14927327 | MOSPD2 |
| NA18946 | hp2 | a0001 | c0001 | t0001 | g0151 | EAS | JPT | MOSPD2_chrX_14868421_14927327 | MOSPD2 |
| NA18947 | hp1 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | MOSPD2_chrX_14868421_14927327 | MOSPD2 |
| NA18947 | hp2 | a0001 | c0001 | t0001 | g0117 | EAS | JPT | MOSPD2_chrX_14868421_14927327 | MOSPD2 |
| NA18948 | hp1 | a0001 | c0001 | t0001 | g0105 | EAS | JPT | MOSPD2_chrX_14868421_14927327 | MOSPD2 |
| NA18950 | hp1 | a0001 | c0001 | t0001 | g0169 | EAS | JPT | MOSPD2_chrX_14868421_14927327 | MOSPD2 |
| NA18950 | hp2 | a0001 | c0001 | t0001 | g0016 | EAS | JPT | MOSPD2_chrX_14868421_14927327 | MOSPD2 |
| NA18952 | hp1 | a0001 | c0001 | t0001 | g0093 | EAS | JPT | MOSPD2_chrX_14868421_14927327 | MOSPD2 |
| NA18953 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | MOSPD2_chrX_14868421_14927327 | MOSPD2 |
| NA18957 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | MOSPD2_chrX_14868421_14927327 | MOSPD2 |
| NA18957 | hp2 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | MOSPD2_chrX_14868421_14927327 | MOSPD2 |
| NA18959 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | MOSPD2_chrX_14868421_14927327 | MOSPD2 |
| NA18960 | hp1 | a0001 | c0001 | t0001 | g0065 | EAS | JPT | MOSPD2_chrX_14868421_14927327 | MOSPD2 |
| NA18961 | hp1 | a0001 | c0001 | t0001 | g0144 | EAS | JPT | MOSPD2_chrX_14868421_14927327 | MOSPD2 |
| NA18962 | hp1 | a0001 | c0001 | t0001 | g0130 | EAS | JPT | MOSPD2_chrX_14868421_14927327 | MOSPD2 |
| NA18965 | hp1 | a0001 | c0001 | t0001 | g0064 | EAS | JPT | MOSPD2_chrX_14868421_14927327 | MOSPD2 |
| NA18966 | hp1 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | MOSPD2_chrX_14868421_14927327 | MOSPD2 |
| NA18967 | hp1 | a0001 | c0001 | t0001 | g0153 | EAS | JPT | MOSPD2_chrX_14868421_14927327 | MOSPD2 |
| NA18969 | hp1 | a0001 | c0001 | t0001 | g0085 | EAS | JPT | MOSPD2_chrX_14868421_14927327 | MOSPD2 |
| NA18969 | hp2 | a0001 | c0001 | t0001 | g0150 | EAS | JPT | MOSPD2_chrX_14868421_14927327 | MOSPD2 |
| NA18970 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | MOSPD2_chrX_14868421_14927327 | MOSPD2 |
| NA18971 | hp1 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | MOSPD2_chrX_14868421_14927327 | MOSPD2 |
| NA18974 | hp1 | a0001 | c0001 | t0001 | g0124 | EAS | JPT | MOSPD2_chrX_14868421_14927327 | MOSPD2 |
| NA18977 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | MOSPD2_chrX_14868421_14927327 | MOSPD2 |
| NA18979 | hp1 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | MOSPD2_chrX_14868421_14927327 | MOSPD2 |
| NA18979 | hp2 | a0001 | c0001 | t0001 | g0174 | EAS | JPT | MOSPD2_chrX_14868421_14927327 | MOSPD2 |
| NA18982 | hp1 | a0001 | c0001 | t0001 | g0048 | EAS | JPT | MOSPD2_chrX_14868421_14927327 | MOSPD2 |
| NA18983 | hp1 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | MOSPD2_chrX_14868421_14927327 | MOSPD2 |
| NA18984 | hp1 | a0001 | c0001 | t0001 | g0097 | EAS | JPT | MOSPD2_chrX_14868421_14927327 | MOSPD2 |
| NA18985 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | MOSPD2_chrX_14868421_14927327 | MOSPD2 |
| NA18986 | hp1 | a0001 | c0001 | t0001 | g0072 | EAS | JPT | MOSPD2_chrX_14868421_14927327 | MOSPD2 |
| NA18988 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | MOSPD2_chrX_14868421_14927327 | MOSPD2 |
| NA18989 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | MOSPD2_chrX_14868421_14927327 | MOSPD2 |
| NA18990 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | MOSPD2_chrX_14868421_14927327 | MOSPD2 |
| NA18994 | hp1 | a0001 | c0001 | t0001 | g0116 | EAS | JPT | MOSPD2_chrX_14868421_14927327 | MOSPD2 |
| NA18995 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | MOSPD2_chrX_14868421_14927327 | MOSPD2 |
| NA18998 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | MOSPD2_chrX_14868421_14927327 | MOSPD2 |
| NA18998 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | MOSPD2_chrX_14868421_14927327 | MOSPD2 |
| NA19000 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | MOSPD2_chrX_14868421_14927327 | MOSPD2 |
| NA19004 | hp1 | a0001 | c0001 | t0001 | g0079 | EAS | JPT | MOSPD2_chrX_14868421_14927327 | MOSPD2 |
| NA19005 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | MOSPD2_chrX_14868421_14927327 | MOSPD2 |
| NA19006 | hp1 | a0001 | c0001 | t0001 | g0050 | EAS | JPT | MOSPD2_chrX_14868421_14927327 | MOSPD2 |
| NA19007 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | MOSPD2_chrX_14868421_14927327 | MOSPD2 |
| NA19009 | hp1 | a0001 | c0001 | t0001 | g0087 | EAS | JPT | MOSPD2_chrX_14868421_14927327 | MOSPD2 |
| NA19012 | hp1 | a0001 | c0001 | t0001 | g0176 | EAS | JPT | MOSPD2_chrX_14868421_14927327 | MOSPD2 |
| NA19030 | hp1 | a0001 | c0001 | t0001 | g0122 | AFR | LWK | MOSPD2_chrX_14868421_14927327 | MOSPD2 |
| NA19030 | hp2 | a0001 | c0001 | t0001 | g0051 | AFR | LWK | MOSPD2_chrX_14868421_14927327 | MOSPD2 |
| NA19043 | hp1 | a0001 | c0001 | t0001 | g0099 | AFR | LWK | MOSPD2_chrX_14868421_14927327 | MOSPD2 |
| NA19055 | hp1 | a0001 | c0001 | t0001 | g0113 | EAS | JPT | MOSPD2_chrX_14868421_14927327 | MOSPD2 |
| NA19056 | hp1 | a0001 | c0001 | t0001 | g0083 | EAS | JPT | MOSPD2_chrX_14868421_14927327 | MOSPD2 |
| NA19058 | hp1 | a0001 | c0001 | t0001 | g0139 | EAS | JPT | MOSPD2_chrX_14868421_14927327 | MOSPD2 |
| NA19060 | hp1 | a0001 | c0001 | t0001 | g0042 | EAS | JPT | MOSPD2_chrX_14868421_14927327 | MOSPD2 |
| NA19062 | hp1 | a0001 | c0001 | t0001 | g0168 | EAS | JPT | MOSPD2_chrX_14868421_14927327 | MOSPD2 |
| NA19063 | hp1 | a0001 | c0001 | t0001 | g0080 | EAS | JPT | MOSPD2_chrX_14868421_14927327 | MOSPD2 |
| NA19066 | hp1 | a0001 | c0001 | t0001 | g0061 | EAS | JPT | MOSPD2_chrX_14868421_14927327 | MOSPD2 |
| NA19067 | hp1 | a0001 | c0001 | t0001 | g0073 | EAS | JPT | MOSPD2_chrX_14868421_14927327 | MOSPD2 |
| NA19068 | hp1 | a0001 | c0001 | t0001 | g0066 | EAS | JPT | MOSPD2_chrX_14868421_14927327 | MOSPD2 |
| NA19070 | hp1 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | MOSPD2_chrX_14868421_14927327 | MOSPD2 |
| NA19072 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | MOSPD2_chrX_14868421_14927327 | MOSPD2 |
| NA19074 | hp1 | a0001 | c0001 | t0001 | g0060 | EAS | JPT | MOSPD2_chrX_14868421_14927327 | MOSPD2 |
| NA19074 | hp2 | a0001 | c0001 | t0001 | g0158 | EAS | JPT | MOSPD2_chrX_14868421_14927327 | MOSPD2 |
| NA19075 | hp1 | a0001 | c0001 | t0001 | g0071 | EAS | JPT | MOSPD2_chrX_14868421_14927327 | MOSPD2 |
| NA19076 | hp1 | a0001 | c0001 | t0001 | g0070 | EAS | JPT | MOSPD2_chrX_14868421_14927327 | MOSPD2 |
| NA19079 | hp1 | a0001 | c0001 | t0001 | g0126 | EAS | JPT | MOSPD2_chrX_14868421_14927327 | MOSPD2 |
| NA19082 | hp1 | a0001 | c0001 | t0001 | g0086 | EAS | JPT | MOSPD2_chrX_14868421_14927327 | MOSPD2 |
| NA19083 | hp1 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | MOSPD2_chrX_14868421_14927327 | MOSPD2 |
| NA19085 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | MOSPD2_chrX_14868421_14927327 | MOSPD2 |
| NA19086 | hp1 | a0001 | c0001 | t0001 | g0078 | EAS | JPT | MOSPD2_chrX_14868421_14927327 | MOSPD2 |
| NA19087 | hp1 | a0001 | c0001 | t0001 | g0082 | EAS | JPT | MOSPD2_chrX_14868421_14927327 | MOSPD2 |
| NA19087 | hp2 | a0001 | c0001 | t0001 | g0053 | EAS | JPT | MOSPD2_chrX_14868421_14927327 | MOSPD2 |
| NA19088 | hp1 | a0001 | c0001 | t0001 | g0063 | EAS | JPT | MOSPD2_chrX_14868421_14927327 | MOSPD2 |
| NA19091 | hp1 | a0001 | c0001 | t0001 | g0177 | EAS | JPT | MOSPD2_chrX_14868421_14927327 | MOSPD2 |
| NA19240 | hp1 | a0001 | c0001 | t0001 | g0030 | AFR | YRI | MOSPD2_chrX_14868421_14927327 | MOSPD2 |
| NA19240 | hp2 | a0001 | c0001 | t0001 | g0057 | AFR | YRI | MOSPD2_chrX_14868421_14927327 | MOSPD2 |
| NA20129 | hp1 | a0001 | c0001 | t0002 | g0011 | AFR | ASW | MOSPD2_chrX_14868421_14927327 | MOSPD2 |
| NA20129 | hp2 | a0001 | c0001 | t0001 | g0043 | AFR | ASW | MOSPD2_chrX_14868421_14927327 | MOSPD2 |
| NA20752 | hp1 | a0001 | c0001 | t0001 | g0017 | EUR | TSI | MOSPD2_chrX_14868421_14927327 | MOSPD2 |
| NA20805 | hp1 | a0001 | c0001 | t0001 | g0019 | EUR | TSI | MOSPD2_chrX_14868421_14927327 | MOSPD2 |
| NA20905 | hp1 | a0001 | c0001 | t0001 | g0059 | SAS | GIH | MOSPD2_chrX_14868421_14927327 | MOSPD2 |
| HG01123 | hp1 | a0001 | c0001 | t0001 | g0024 | AMR | CLM | MOSPD2_chrX_14868421_14927327 | MOSPD2 |
| HG01123 | hp2 | a0001 | c0001 | t0001 | g0017 | AMR | CLM | MOSPD2_chrX_14868421_14927327 | MOSPD2 |
| HG02109 | hp1 | a0001 | c0001 | t0001 | g0129 | AFR | ACB | MOSPD2_chrX_14868421_14927327 | MOSPD2 |
| HG02109 | hp2 | a0001 | c0001 | t0002 | g0031 | AFR | ACB | MOSPD2_chrX_14868421_14927327 | MOSPD2 |
| HG02486 | hp1 | a0001 | c0001 | t0002 | g0031 | AFR | ACB | MOSPD2_chrX_14868421_14927327 | MOSPD2 |
| HG03471 | hp1 | a0001 | c0001 | t0001 | g0054 | AFR | MSL | MOSPD2_chrX_14868421_14927327 | MOSPD2 |
| HG06807 | hp1 | a0001 | c0001 | t0008 | g0162 | AFR | USA | MOSPD2_chrX_14868421_14927327 | MOSPD2 |
| HG06807 | hp2 | a0001 | c0001 | t0001 | g0196 | AFR | USA | MOSPD2_chrX_14868421_14927327 | MOSPD2 |
| NA18955 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | MOSPD2_chrX_14868421_14927327 | MOSPD2 |
| NA20300 | hp1 | a0001 | c0001 | t0001 | g0123 | AFR | USA | MOSPD2_chrX_14868421_14927327 | MOSPD2 |
| NA20300 | hp2 | a0001 | c0001 | t0001 | g0173 | AFR | USA | MOSPD2_chrX_14868421_14927327 | MOSPD2 |
| NA21309 | hp1 | a0001 | c0001 | t0001 | g0131 | AFR | LWK | MOSPD2_chrX_14868421_14927327 | MOSPD2 |
| NA21309 | hp2 | a0001 | c0001 | t0002 | g0203 | AFR | LWK | MOSPD2_chrX_14868421_14927327 | MOSPD2 |
| homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0001 | g0171 | REF | REF | MOSPD2_chrX_14868421_14927327 | MOSPD2 |
| homoSapiens_grch38 | hp1 | a0001 | c0001 | t0001 | g0125 | REF | REF | MOSPD2_chrX_14868421_14927327 | MOSPD2 |
| chr:pos | ref | alt | # # of ahapid:amio-acid(protein) level
|
ahapids | # # of haplotypeids
|
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna_pos_length | cds_pos_length | aa_pos_length | distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chrX:14911253
|
G | A | 1 | a0002 | 4 | HG00280.hp1 HG01261.hp1 HG01516.hp2 others(1): Show |
missense_variant | MODERATE | c.719G>A | p.Ser240Asn | MOSPD2 | ENSG00000130150.12 | transcript | ENST00000380492.8 | protein_coding | 9/15 | 827/4183 | 719/1557 | 240/518 | chrX | 14911253 |
| chr:pos | ref | alt | # # of chapid
|
chapids | # # of haplotypeids
|
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna_pos_length | cds_pos_length | aa_pos_length | distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chrX:14908936
|
C | T | 1 | a0001c0003 | 3 | HG01168.hp2 HG01169.hp2 HG01175.hp1 |
synonymous_variant | LOW | c.654C>T | p.Val218Val | MOSPD2 | ENSG00000130150.12 | transcript | ENST00000380492.8 | protein_coding | 8/15 | 762/4183 | 654/1557 | 218/518 | chrX | 14908936 | ||
| chrX:14912260
|
C | T | 1 | a0001c0004 | 1 | HG02630.hp1 | synonymous_variant | LOW | c.891C>T | p.Thr297Thr | MOSPD2 | ENSG00000130150.12 | transcript | ENST00000380492.8 | protein_coding | 10/15 | 999/4183 | 891/1557 | 297/518 | chrX | 14912260 |
| 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_pos_length | cds_pos_length | aa_pos_length | distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chrX:14873473
|
C | T | 1 | a0001c0001t0005 | 2 | HG01167.hp1 HG01169.hp1 |
5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-56C>T | MOSPD2 | ENSG00000130150.12 | transcript | ENST00000380492.8 | protein_coding | 1/15 | chrX | 14873473 | ||||||
| chrX:14919843
|
C | T | 1 | a0001c0001t0012 | 1 | HG01192.hp1 | 3_prime_UTR_variant | MODIFIER | c.*34C>T | MOSPD2 | ENSG00000130150.12 | transcript | ENST00000380492.8 | protein_coding | 15/15 | 34 | chrX | 14919843 | |||||
| chrX:14919937
|
G | A | 1 | a0001c0001t0002 | 17 | HG01106.hp1 HG01243.hp1 HG01891.hp1 others(14): Show |
3_prime_UTR_variant | MODIFIER | c.*128G>A | MOSPD2 | ENSG00000130150.12 | transcript | ENST00000380492.8 | protein_coding | 15/15 | 128 | chrX | 14919937 | |||||
| chrX:14920027
|
T | C | 1 | a0001c0001t0006 | 1 | HG01099.hp1 | 3_prime_UTR_variant | MODIFIER | c.*218T>C | MOSPD2 | ENSG00000130150.12 | transcript | ENST00000380492.8 | protein_coding | 15/15 | 218 | chrX | 14920027 | |||||
| chrX:14920199
|
T | C | 1 | a0001c0001t0004 | 3 | HG02809.hp1 HG02922.hp1 HG03041.hp2 |
3_prime_UTR_variant | MODIFIER | c.*390T>C | MOSPD2 | ENSG00000130150.12 | transcript | ENST00000380492.8 | protein_coding | 15/15 | 390 | chrX | 14920199 | |||||
| chrX:14920242
|
T | C | 1 | a0001c0001t0007 | 1 | HG03669.hp2 | 3_prime_UTR_variant | MODIFIER | c.*433T>C | MOSPD2 | ENSG00000130150.12 | transcript | ENST00000380492.8 | protein_coding | 15/15 | 433 | chrX | 14920242 | |||||
| chrX:14920490
|
AG | A | 2 | a0001c0001t0003a0001c0001t0011 | 15 | HG01074.hp1 HG01884.hp1 HG01891.hp2 others(12): Show |
3_prime_UTR_variant | MODIFIER | c.*682delG | MOSPD2 | ENSG00000130150.12 | transcript | ENST00000380492.8 | protein_coding | 15/15 | 682 | chrX | 14920490 | |||||
| chrX:14920492
|
C | T | 2 | a0001c0001t0003a0001c0001t0011 | 15 | HG01074.hp1 HG01884.hp1 HG01891.hp2 others(12): Show |
3_prime_UTR_variant | MODIFIER | c.*683C>T | MOSPD2 | ENSG00000130150.12 | transcript | ENST00000380492.8 | protein_coding | 15/15 | 683 | chrX | 14920492 | |||||
| chrX:14920493
|
G | T | 2 | a0001c0001t0003a0001c0001t0011 | 15 | HG01074.hp1 HG01884.hp1 HG01891.hp2 others(12): Show |
3_prime_UTR_variant | MODIFIER | c.*684G>T | MOSPD2 | ENSG00000130150.12 | transcript | ENST00000380492.8 | protein_coding | 15/15 | 684 | chrX | 14920493 | |||||
| chrX:14920677
|
A | G | 1 | a0001c0001t0010 | 1 | HG01175.hp2 | 3_prime_UTR_variant | MODIFIER | c.*868A>G | MOSPD2 | ENSG00000130150.12 | transcript | ENST00000380492.8 | protein_coding | 15/15 | 868 | chrX | 14920677 | |||||
| chrX:14920762
|
A | G | 1 | a0001c0001t0011 | 1 | HG01891.hp2 | 3_prime_UTR_variant | MODIFIER | c.*953A>G | MOSPD2 | ENSG00000130150.12 | transcript | ENST00000380492.8 | protein_coding | 15/15 | 953 | chrX | 14920762 | |||||
| chrX:14920881
|
AAAAAT | A | 1 | a0001c0001t0008 | 1 | HG06807.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1077_*1081delTAAA others(1): Show |
MOSPD2 | ENSG00000130150.12 | transcript | ENST00000380492.8 | protein_coding | 15/15 | 1077 | INFO_REALIGN_3_PRIME | chrX | 14920881 | ||||
| chrX:14921956
|
G | GAAAT | 1 | a0001c0001t0009 | 1 | HG01256.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2148_*2151dupAAAT | MOSPD2 | ENSG00000130150.12 | transcript | ENST00000380492.8 | protein_coding | 15/15 | 2152 | INFO_REALIGN_3_PRIME | chrX | 14921956 |
| 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_pos_length | cds_pos_length | aa_pos_length | distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chrX:14874119
|
G | A | 1 | a0001c0001t0002g0011 | 2 | HG02970.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.79+361G>A | MOSPD2 | ENSG00000130150.12 | transcript | ENST00000380492.8 | protein_coding | 2/14 | chrX | 14874119 | ||||||
| chrX:14874136
|
T | C | 2 | a0001c0001t0002g0003a0001c0001t0002g0012 | 6 | HG01106.hp1 HG01891.hp1 HG02280.hp2 others(3): Show |
intron_variant | MODIFIER | c.79+378T>C | MOSPD2 | ENSG00000130150.12 | transcript | ENST00000380492.8 | protein_coding | 2/14 | chrX | 14874136 | ||||||
| chrX:14874403
|
C | T | 1 | a0001c0001t0001g0206 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.79+645C>T | MOSPD2 | ENSG00000130150.12 | transcript | ENST00000380492.8 | protein_coding | 2/14 | chrX | 14874403 | ||||||
| chrX:14874411
|
CTT | C | 1 | a0001c0001t0001g0032 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.79+654_79+655delTT | MOSPD2 | ENSG00000130150.12 | transcript | ENST00000380492.8 | protein_coding | 2/14 | chrX | 14874411 | ||||||
| chrX:14874736
|
T | C | 1 | a0001c0001t0007g0033 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.79+978T>C | MOSPD2 | ENSG00000130150.12 | transcript | ENST00000380492.8 | protein_coding | 2/14 | chrX | 14874736 | ||||||
| chrX:14875053
|
G | A | 4 | a0002c0002t0001g0034a0002c0002t0001g0035a0002c0002t0001g0036others(1): Show | 4 | HG00280.hp1 HG01261.hp1 HG01516.hp2 others(1): Show |
intron_variant | MODIFIER | c.79+1295G>A | MOSPD2 | ENSG00000130150.12 | transcript | ENST00000380492.8 | protein_coding | 2/14 | chrX | 14875053 | ||||||
| chrX:14875235
|
A | C | 1 | a0001c0001t0007g0033 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.79+1477A>C | MOSPD2 | ENSG00000130150.12 | transcript | ENST00000380492.8 | protein_coding | 2/14 | chrX | 14875235 | ||||||
| chrX:14875527
|
A | G | 1 | a0001c0001t0001g0205 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.79+1769A>G | MOSPD2 | ENSG00000130150.12 | transcript | ENST00000380492.8 | protein_coding | 2/14 | chrX | 14875527 | ||||||
| chrX:14875533
|
C | T | 5 | a0001c0001t0002g0003a0001c0001t0002g0012a0001c0001t0002g0031others(2): Show | 10 | HG01106.hp1 HG01891.hp1 HG02109.hp2 others(7): Show |
intron_variant | MODIFIER | c.79+1775C>T | MOSPD2 | ENSG00000130150.12 | transcript | ENST00000380492.8 | protein_coding | 2/14 | chrX | 14875533 | ||||||
| chrX:14875751
|
A | G | 1 | a0001c0001t0002g0204 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.79+1993A>G | MOSPD2 | ENSG00000130150.12 | transcript | ENST00000380492.8 | protein_coding | 2/14 | chrX | 14875751 | ||||||
| chrX:14875914
|
G | A | 11 | a0001c0001t0001g0038a0001c0001t0002g0003a0001c0001t0002g0006others(8): Show | 19 | HG01106.hp1 HG01243.hp1 HG01891.hp1 others(16): Show |
intron_variant | MODIFIER | c.79+2156G>A | MOSPD2 | ENSG00000130150.12 | transcript | ENST00000380492.8 | protein_coding | 2/14 | chrX | 14875914 | ||||||
| chrX:14875960
|
C | CT | 4 | a0001c0001t0001g0030a0001c0001t0004g0200a0001c0001t0004g0201others(1): Show | 5 | HG02717.hp1 HG02809.hp1 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.79+2204dupT | MOSPD2 | ENSG00000130150.12 | transcript | ENST00000380492.8 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chrX | 14875960 | |||||
| chrX:14876240
|
A | C | 4 | a0001c0001t0002g0006a0001c0001t0002g0011a0001c0001t0002g0039others(1): Show | 7 | HG01243.hp1 HG02280.hp1 HG02622.hp2 others(4): Show |
intron_variant | MODIFIER | c.79+2482A>C | MOSPD2 | ENSG00000130150.12 | transcript | ENST00000380492.8 | protein_coding | 2/14 | chrX | 14876240 | ||||||
| chrX:14876286
|
C | T | 1 | a0001c0001t0002g0204 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.79+2528C>T | MOSPD2 | ENSG00000130150.12 | transcript | ENST00000380492.8 | protein_coding | 2/14 | chrX | 14876286 | ||||||
| chrX:14876529
|
T | G | 1 | a0001c0001t0007g0033 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.79+2771T>G | MOSPD2 | ENSG00000130150.12 | transcript | ENST00000380492.8 | protein_coding | 2/14 | chrX | 14876529 | ||||||
| chrX:14876536
|
CT | C | 2 | a0001c0001t0003g0007a0001c0001t0003g0041 | 4 | HG01074.hp1 HG02293.hp1 HG02622.hp1 others(1): Show |
intron_variant | MODIFIER | c.79+2779delT | MOSPD2 | ENSG00000130150.12 | transcript | ENST00000380492.8 | protein_coding | 2/14 | chrX | 14876536 | ||||||
| chrX:14876622
|
T | G | 1 | a0001c0001t0001g0042 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.79+2864T>G | MOSPD2 | ENSG00000130150.12 | transcript | ENST00000380492.8 | protein_coding | 2/14 | chrX | 14876622 | ||||||
| chrX:14876688
|
T | A | 4 | a0001c0001t0002g0006a0001c0001t0002g0011a0001c0001t0002g0039others(1): Show | 7 | HG01243.hp1 HG02280.hp1 HG02622.hp2 others(4): Show |
intron_variant | MODIFIER | c.79+2930T>A | MOSPD2 | ENSG00000130150.12 | transcript | ENST00000380492.8 | protein_coding | 2/14 | chrX | 14876688 | ||||||
| chrX:14876824
|
A | T | 1 | a0001c0001t0001g0199 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.79+3066A>T | MOSPD2 | ENSG00000130150.12 | transcript | ENST00000380492.8 | protein_coding | 2/14 | chrX | 14876824 | ||||||
| chrX:14877054
|
T | C | 4 | a0001c0001t0001g0043a0001c0001t0001g0044a0001c0001t0001g0045others(1): Show | 4 | HG03139.hp1 HG03516.hp2 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.79+3296T>C | MOSPD2 | ENSG00000130150.12 | transcript | ENST00000380492.8 | protein_coding | 2/14 | chrX | 14877054 | ||||||
| chrX:14877098
|
A | T | 1 | a0001c0001t0003g0198 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.79+3340A>T | MOSPD2 | ENSG00000130150.12 | transcript | ENST00000380492.8 | protein_coding | 2/14 | chrX | 14877098 | ||||||
| chrX:14877419
|
C | T | 3 | a0001c0001t0001g0195a0001c0001t0001g0196a0001c0001t0001g0197 | 3 | HG03041.hp1 HG06807.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.79+3661C>T | MOSPD2 | ENSG00000130150.12 | transcript | ENST00000380492.8 | protein_coding | 2/14 | chrX | 14877419 | ||||||
| chrX:14877584
|
G | C | 1 | a0001c0001t0001g0047 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.79+3826G>C | MOSPD2 | ENSG00000130150.12 | transcript | ENST00000380492.8 | protein_coding | 2/14 | chrX | 14877584 | ||||||
| chrX:14877620
|
C | T | 2 | a0001c0001t0001g0028a0001c0001t0001g0029 | 4 | HG02630.hp2 HG02809.hp2 HG02895.hp1 others(1): Show |
intron_variant | MODIFIER | c.79+3862C>T | MOSPD2 | ENSG00000130150.12 | transcript | ENST00000380492.8 | protein_coding | 2/14 | chrX | 14877620 | ||||||
| chrX:14877647
|
C | CT | 9 | a0001c0001t0001g0027a0001c0001t0001g0187a0001c0001t0001g0188others(6): Show | 10 | HG00639.hp1 HG00733.hp1 HG00735.hp1 others(7): Show |
intron_variant | MODIFIER | c.79+3895dupT | MOSPD2 | ENSG00000130150.12 | transcript | ENST00000380492.8 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chrX | 14877647 | |||||
| chrX:14877688
|
T | C | 1 | a0001c0001t0001g0048 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.79+3930T>C | MOSPD2 | ENSG00000130150.12 | transcript | ENST00000380492.8 | protein_coding | 2/14 | chrX | 14877688 | ||||||
| chrX:14877800
|
T | C | 4 | a0001c0001t0002g0006a0001c0001t0002g0011a0001c0001t0002g0039others(1): Show | 7 | HG01243.hp1 HG02280.hp1 HG02622.hp2 others(4): Show |
intron_variant | MODIFIER | c.79+4042T>C | MOSPD2 | ENSG00000130150.12 | transcript | ENST00000380492.8 | protein_coding | 2/14 | chrX | 14877800 | ||||||
| chrX:14877817
|
C | CA | 5 | a0001c0001t0001g0038a0001c0001t0001g0049a0001c0001t0001g0050others(2): Show | 5 | HG01934.hp1 HG02148.hp1 HG02723.hp2 others(2): Show |
intron_variant | MODIFIER | c.79+4073dupA | MOSPD2 | ENSG00000130150.12 | transcript | ENST00000380492.8 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chrX | 14877817 | |||||
| chrX:14877908
|
G | A | 1 | a0001c0001t0002g0011 | 2 | HG02970.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.79+4150G>A | MOSPD2 | ENSG00000130150.12 | transcript | ENST00000380492.8 | protein_coding | 2/14 | chrX | 14877908 | ||||||
| chrX:14877961
|
G | C | 1 | a0001c0001t0001g0053 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.79+4203G>C | MOSPD2 | ENSG00000130150.12 | transcript | ENST00000380492.8 | protein_coding | 2/14 | chrX | 14877961 | ||||||
| chrX:14877995
|
C | T | 11 | a0001c0001t0001g0038a0001c0001t0002g0003a0001c0001t0002g0006others(8): Show | 19 | HG01106.hp1 HG01243.hp1 HG01891.hp1 others(16): Show |
intron_variant | MODIFIER | c.79+4237C>T | MOSPD2 | ENSG00000130150.12 | transcript | ENST00000380492.8 | protein_coding | 2/14 | chrX | 14877995 | ||||||
| chrX:14878012
|
A | G | 112 | a0001c0001t0001g0004a0001c0001t0001g0010a0001c0001t0001g0024others(109): Show | 136 | HG00140.hp1 HG00280.hp1 HG00408.hp2 others(133): Show |
intron_variant | MODIFIER | c.79+4254A>G | MOSPD2 | ENSG00000130150.12 | transcript | ENST00000380492.8 | protein_coding | 2/14 | chrX | 14878012 | ||||||
| chrX:14878037
|
T | C | 1 | a0001c0001t0001g0054 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.79+4279T>C | MOSPD2 | ENSG00000130150.12 | transcript | ENST00000380492.8 | protein_coding | 2/14 | chrX | 14878037 | ||||||
| chrX:14878316
|
C | T | 4 | a0001c0001t0002g0006a0001c0001t0002g0011a0001c0001t0002g0039others(1): Show | 7 | HG01243.hp1 HG02280.hp1 HG02622.hp2 others(4): Show |
intron_variant | MODIFIER | c.79+4558C>T | MOSPD2 | ENSG00000130150.12 | transcript | ENST00000380492.8 | protein_coding | 2/14 | chrX | 14878316 | ||||||
| chrX:14878411
|
G | A | 1 | a0001c0001t0001g0055 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.79+4653G>A | MOSPD2 | ENSG00000130150.12 | transcript | ENST00000380492.8 | protein_coding | 2/14 | chrX | 14878411 | ||||||
| chrX:14878476
|
CA | C | 6 | a0001c0001t0003g0005a0001c0001t0003g0026a0001c0001t0003g0184others(3): Show | 10 | HG01884.hp1 HG02145.hp1 HG02258.hp1 others(7): Show |
intron_variant | MODIFIER | c.79+4719delA | MOSPD2 | ENSG00000130150.12 | transcript | ENST00000380492.8 | protein_coding | 2/14 | chrX | 14878476 | ||||||
| chrX:14878507
|
G | T | 2 | a0001c0001t0001g0025a0001c0001t0001g0183 | 3 | HG00733.hp2 HG01069.hp1 HG01071.hp2 |
intron_variant | MODIFIER | c.79+4749G>T | MOSPD2 | ENSG00000130150.12 | transcript | ENST00000380492.8 | protein_coding | 2/14 | chrX | 14878507 | ||||||
| chrX:14878745
|
A | T | 26 | a0001c0001t0001g0027a0001c0001t0001g0167a0001c0001t0001g0168others(23): Show | 27 | HG00558.hp2 HG00609.hp1 HG00639.hp1 others(24): Show |
intron_variant | MODIFIER | c.79+4987A>T | MOSPD2 | ENSG00000130150.12 | transcript | ENST00000380492.8 | protein_coding | 2/14 | chrX | 14878745 | ||||||
| chrX:14878746
|
C | T | 3 | a0001c0001t0002g0006a0001c0001t0002g0039a0001c0001t0002g0040 | 5 | HG01243.hp1 HG02280.hp1 HG02622.hp2 others(2): Show |
intron_variant | MODIFIER | c.79+4988C>T | MOSPD2 | ENSG00000130150.12 | transcript | ENST00000380492.8 | protein_coding | 2/14 | chrX | 14878746 | ||||||
| chrX:14878775
|
C | T | 3 | a0001c0001t0001g0164a0001c0001t0001g0166a0001c0004t0001g0165 | 3 | HG02630.hp1 HG02723.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.79+5017C>T | MOSPD2 | ENSG00000130150.12 | transcript | ENST00000380492.8 | protein_coding | 2/14 | chrX | 14878775 | ||||||
| chrX:14878780
|
T | C | 1 | a0001c0001t0007g0033 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.79+5022T>C | MOSPD2 | ENSG00000130150.12 | transcript | ENST00000380492.8 | protein_coding | 2/14 | chrX | 14878780 | ||||||
| chrX:14878808
|
T | C | 3 | a0001c0001t0001g0043a0001c0001t0001g0044a0001c0001t0001g0045 | 3 | HG03139.hp1 HG03516.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.79+5050T>C | MOSPD2 | ENSG00000130150.12 | transcript | ENST00000380492.8 | protein_coding | 2/14 | chrX | 14878808 | ||||||
| chrX:14878847
|
T | C | 1 | a0001c0001t0003g0184 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.79+5089T>C | MOSPD2 | ENSG00000130150.12 | transcript | ENST00000380492.8 | protein_coding | 2/14 | chrX | 14878847 | ||||||
| chrX:14879248
|
C | A | 1 | a0001c0001t0001g0056 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.79+5490C>A | MOSPD2 | ENSG00000130150.12 | transcript | ENST00000380492.8 | protein_coding | 2/14 | chrX | 14879248 | ||||||
| chrX:14879450
|
G | A | 1 | a0001c0001t0001g0057 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.79+5692G>A | MOSPD2 | ENSG00000130150.12 | transcript | ENST00000380492.8 | protein_coding | 2/14 | chrX | 14879450 | ||||||
| chrX:14879870
|
T | G | 1 | a0001c0001t0001g0030 | 2 | HG02717.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.79+6112T>G | MOSPD2 | ENSG00000130150.12 | transcript | ENST00000380492.8 | protein_coding | 2/14 | chrX | 14879870 | ||||||
| chrX:14880101
|
G | A | 1 | a0001c0001t0001g0058 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.79+6343G>A | MOSPD2 | ENSG00000130150.12 | transcript | ENST00000380492.8 | protein_coding | 2/14 | chrX | 14880101 | ||||||
| chrX:14880116
|
A | G | 1 | a0001c0001t0001g0126 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.79+6358A>G | MOSPD2 | ENSG00000130150.12 | transcript | ENST00000380492.8 | protein_coding | 2/14 | chrX | 14880116 | ||||||
| chrX:14880148
|
T | C | 1 | a0001c0003t0001g0023 | 2 | HG01168.hp2 HG01169.hp2 |
intron_variant | MODIFIER | c.79+6390T>C | MOSPD2 | ENSG00000130150.12 | transcript | ENST00000380492.8 | protein_coding | 2/14 | chrX | 14880148 | ||||||
| chrX:14880276
|
A | G | 1 | a0001c0001t0001g0163 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.79+6518A>G | MOSPD2 | ENSG00000130150.12 | transcript | ENST00000380492.8 | protein_coding | 2/14 | chrX | 14880276 | ||||||
| chrX:14880381
|
A | G | 4 | a0001c0001t0001g0164a0001c0001t0001g0166a0001c0001t0008g0162others(1): Show | 4 | HG02630.hp1 HG02723.hp1 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.79+6623A>G | MOSPD2 | ENSG00000130150.12 | transcript | ENST00000380492.8 | protein_coding | 2/14 | chrX | 14880381 | ||||||
| chrX:14880552
|
A | G | 108 | a0001c0001t0001g0004a0001c0001t0001g0010a0001c0001t0001g0024others(105): Show | 132 | HG00140.hp1 HG00280.hp1 HG00408.hp2 others(129): Show |
intron_variant | MODIFIER | c.79+6794A>G | MOSPD2 | ENSG00000130150.12 | transcript | ENST00000380492.8 | protein_coding | 2/14 | chrX | 14880552 | ||||||
| chrX:14880990
|
G | C | 4 | a0001c0001t0002g0006a0001c0001t0002g0011a0001c0001t0002g0039others(1): Show | 7 | HG01243.hp1 HG02280.hp1 HG02622.hp2 others(4): Show |
intron_variant | MODIFIER | c.79+7232G>C | MOSPD2 | ENSG00000130150.12 | transcript | ENST00000380492.8 | protein_coding | 2/14 | chrX | 14880990 | ||||||
| chrX:14881071
|
T | C | 206 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(203): Show | 267 | HG00140.hp1 HG00280.hp1 HG00408.hp1 others(264): Show |
intron_variant | MODIFIER | c.79+7313T>C | MOSPD2 | ENSG00000130150.12 | transcript | ENST00000380492.8 | protein_coding | 2/14 | chrX | 14881071 | ||||||
| chrX:14881087
|
T | G | 1 | a0001c0001t0001g0059 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.79+7329T>G | MOSPD2 | ENSG00000130150.12 | transcript | ENST00000380492.8 | protein_coding | 2/14 | chrX | 14881087 | ||||||
| chrX:14881216
|
A | G | 4 | a0001c0001t0001g0164a0001c0001t0001g0166a0001c0001t0008g0162others(1): Show | 4 | HG02630.hp1 HG02723.hp1 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.79+7458A>G | MOSPD2 | ENSG00000130150.12 | transcript | ENST00000380492.8 | protein_coding | 2/14 | chrX | 14881216 | ||||||
| chrX:14881235
|
C | CT | 2 | a0001c0001t0003g0186a0001c0001t0007g0033 | 2 | HG01884.hp1 HG03669.hp2 |
intron_variant | MODIFIER | c.79+7489dupT | MOSPD2 | ENSG00000130150.12 | transcript | ENST00000380492.8 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chrX | 14881235 | |||||
| chrX:14881257
|
A | G | 1 | a0001c0001t0001g0124 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.79+7499A>G | MOSPD2 | ENSG00000130150.12 | transcript | ENST00000380492.8 | protein_coding | 2/14 | chrX | 14881257 | ||||||
| chrX:14881287
|
A | C | 3 | a0001c0001t0001g0164a0001c0001t0001g0166a0001c0004t0001g0165 | 3 | HG02630.hp1 HG02723.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.79+7529A>C | MOSPD2 | ENSG00000130150.12 | transcript | ENST00000380492.8 | protein_coding | 2/14 | chrX | 14881287 | ||||||
| chrX:14881559
|
C | G | 5 | a0001c0001t0002g0003a0001c0001t0002g0012a0001c0001t0002g0031others(2): Show | 10 | HG01106.hp1 HG01891.hp1 HG02109.hp2 others(7): Show |
intron_variant | MODIFIER | c.79+7801C>G | MOSPD2 | ENSG00000130150.12 | transcript | ENST00000380492.8 | protein_coding | 2/14 | chrX | 14881559 | ||||||
| chrX:14881799
|
A | G | 1 | a0001c0001t0001g0166 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.79+8041A>G | MOSPD2 | ENSG00000130150.12 | transcript | ENST00000380492.8 | protein_coding | 2/14 | chrX | 14881799 | ||||||
| chrX:14882026
|
G | C | 6 | a0001c0001t0001g0038a0001c0001t0002g0003a0001c0001t0002g0012others(3): Show | 11 | HG01106.hp1 HG01891.hp1 HG02109.hp2 others(8): Show |
intron_variant | MODIFIER | c.79+8268G>C | MOSPD2 | ENSG00000130150.12 | transcript | ENST00000380492.8 | protein_coding | 2/14 | chrX | 14882026 | ||||||
| chrX:14882203
|
G | T | 30 | a0001c0001t0001g0020a0001c0001t0001g0021a0001c0001t0001g0022others(27): Show | 43 | HG01070.hp2 HG01071.hp1 HG01106.hp1 others(40): Show |
intron_variant | MODIFIER | c.79+8445G>T | MOSPD2 | ENSG00000130150.12 | transcript | ENST00000380492.8 | protein_coding | 2/14 | chrX | 14882203 | ||||||
| chrX:14882247
|
C | T | 2 | a0001c0001t0001g0160a0001c0001t0001g0161 | 2 | HG02056.hp1 NA18747.hp1 |
intron_variant | MODIFIER | c.79+8489C>T | MOSPD2 | ENSG00000130150.12 | transcript | ENST00000380492.8 | protein_coding | 2/14 | chrX | 14882247 | ||||||
| chrX:14882366
|
GA | G | 1 | a0001c0001t0001g0205 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.79+8609delA | MOSPD2 | ENSG00000130150.12 | transcript | ENST00000380492.8 | protein_coding | 2/14 | chrX | 14882366 | ||||||
| chrX:14882372
|
T | C | 4 | a0001c0001t0001g0127a0001c0001t0001g0128a0001c0001t0001g0129others(1): Show | 4 | HG01109.hp1 HG02109.hp1 HG02976.hp1 others(1): Show |
intron_variant | MODIFIER | c.79+8614T>C | MOSPD2 | ENSG00000130150.12 | transcript | ENST00000380492.8 | protein_coding | 2/14 | chrX | 14882372 | ||||||
| chrX:14882447
|
T | C | 1 | a0001c0001t0001g0164 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.79+8689T>C | MOSPD2 | ENSG00000130150.12 | transcript | ENST00000380492.8 | protein_coding | 2/14 | chrX | 14882447 | ||||||
| chrX:14882628
|
A | T | 1 | a0001c0001t0001g0117 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.79+8870A>T | MOSPD2 | ENSG00000130150.12 | transcript | ENST00000380492.8 | protein_coding | 2/14 | chrX | 14882628 | ||||||
| chrX:14882677
|
T | C | 5 | a0001c0001t0001g0042a0001c0001t0001g0060a0001c0001t0001g0061others(2): Show | 5 | NA18612.hp1 NA19060.hp1 NA19066.hp1 others(2): Show |
intron_variant | MODIFIER | c.79+8919T>C | MOSPD2 | ENSG00000130150.12 | transcript | ENST00000380492.8 | protein_coding | 2/14 | chrX | 14882677 | ||||||
| chrX:14882807
|
C | CT | 2 | a0001c0001t0001g0030a0001c0001t0007g0033 | 3 | HG02717.hp1 HG03669.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.79+9063dupT | MOSPD2 | ENSG00000130150.12 | transcript | ENST00000380492.8 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chrX | 14882807 | |||||
| chrX:14882807
|
CT | C | 4 | a0001c0001t0001g0064a0001c0001t0001g0130a0001c0001t0001g0187others(1): Show | 4 | HG00639.hp1 NA18522.hp1 NA18962.hp1 others(1): Show |
intron_variant | MODIFIER | c.79+9063delT | MOSPD2 | ENSG00000130150.12 | transcript | ENST00000380492.8 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chrX | 14882807 | |||||
| chrX:14882935
|
G | A | 1 | a0001c0001t0001g0065 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.79+9177G>A | MOSPD2 | ENSG00000130150.12 | transcript | ENST00000380492.8 | protein_coding | 2/14 | chrX | 14882935 | ||||||
| chrX:14883051
|
C | T | 1 | a0001c0001t0007g0033 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.79+9293C>T | MOSPD2 | ENSG00000130150.12 | transcript | ENST00000380492.8 | protein_coding | 2/14 | chrX | 14883051 | ||||||
| chrX:14883105
|
G | A | 1 | a0001c0001t0001g0131 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.79+9347G>A | MOSPD2 | ENSG00000130150.12 | transcript | ENST00000380492.8 | protein_coding | 2/14 | chrX | 14883105 | ||||||
| chrX:14883117
|
C | T | 2 | a0001c0001t0001g0158a0001c0001t0001g0159 | 2 | HG00423.hp2 NA19074.hp2 |
intron_variant | MODIFIER | c.79+9359C>T | MOSPD2 | ENSG00000130150.12 | transcript | ENST00000380492.8 | protein_coding | 2/14 | chrX | 14883117 | ||||||
| chrX:14883194
|
GA | G | 1 | a0001c0001t0001g0123 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.79+9447delA | MOSPD2 | ENSG00000130150.12 | transcript | ENST00000380492.8 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chrX | 14883194 | |||||
| chrX:14884172
|
G | GA | 2 | a0001c0001t0001g0066a0001c0001t0001g0132 | 2 | HG01361.hp1 NA19068.hp1 |
intron_variant | MODIFIER | c.80-8540dupA | MOSPD2 | ENSG00000130150.12 | transcript | ENST00000380492.8 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chrX | 14884172 | |||||
| chrX:14884431
|
G | A | 3 | a0001c0001t0002g0006a0001c0001t0002g0039a0001c0001t0002g0040 | 5 | HG01243.hp1 HG02280.hp1 HG02622.hp2 others(2): Show |
intron_variant | MODIFIER | c.80-8292G>A | MOSPD2 | ENSG00000130150.12 | transcript | ENST00000380492.8 | protein_coding | 2/14 | chrX | 14884431 | ||||||
| chrX:14884585
|
G | T | 10 | a0001c0001t0001g0038a0001c0001t0002g0003a0001c0001t0002g0006others(7): Show | 18 | HG01106.hp1 HG01243.hp1 HG01891.hp1 others(15): Show |
intron_variant | MODIFIER | c.80-8138G>T | MOSPD2 | ENSG00000130150.12 | transcript | ENST00000380492.8 | protein_coding | 2/14 | chrX | 14884585 | ||||||
| chrX:14884767
|
A | C | 98 | a0001c0001t0001g0004a0001c0001t0001g0010a0001c0001t0001g0024others(95): Show | 114 | HG00140.hp1 HG00280.hp1 HG00408.hp2 others(111): Show |
intron_variant | MODIFIER | c.80-7956A>C | MOSPD2 | ENSG00000130150.12 | transcript | ENST00000380492.8 | protein_coding | 2/14 | chrX | 14884767 | ||||||
| chrX:14884922
|
A | AT | 3 | a0001c0001t0001g0164a0001c0001t0001g0166a0001c0004t0001g0165 | 3 | HG02630.hp1 HG02723.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.80-7801_80-7800ins others(1): Show |
MOSPD2 | ENSG00000130150.12 | transcript | ENST00000380492.8 | protein_coding | 2/14 | chrX | 14884922 | ||||||
| chrX:14884951
|
C | A | 7 | a0001c0001t0001g0027a0001c0001t0001g0187a0001c0001t0001g0188others(4): Show | 8 | HG00639.hp1 HG00735.hp1 HG01081.hp1 others(5): Show |
intron_variant | MODIFIER | c.80-7772C>A | MOSPD2 | ENSG00000130150.12 | transcript | ENST00000380492.8 | protein_coding | 2/14 | chrX | 14884951 | ||||||
| chrX:14884973
|
TA | T | 1 | a0001c0001t0001g0030 | 2 | HG02717.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.80-7749delA | MOSPD2 | ENSG00000130150.12 | transcript | ENST00000380492.8 | protein_coding | 2/14 | chrX | 14884973 | ||||||
| chrX:14885167
|
T | G | 1 | a0001c0001t0002g0204 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.80-7556T>G | MOSPD2 | ENSG00000130150.12 | transcript | ENST00000380492.8 | protein_coding | 2/14 | chrX | 14885167 | ||||||
| chrX:14885543
|
A | G | 1 | a0001c0001t0001g0166 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.80-7180A>G | MOSPD2 | ENSG00000130150.12 | transcript | ENST00000380492.8 | protein_coding | 2/14 | chrX | 14885543 | ||||||
| chrX:14885604
|
G | A | 1 | a0001c0001t0001g0067 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.80-7119G>A | MOSPD2 | ENSG00000130150.12 | transcript | ENST00000380492.8 | protein_coding | 2/14 | chrX | 14885604 | ||||||
| chrX:14885790
|
CTT | C | 1 | a0001c0001t0001g0068 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.80-6932_80-6931del others(2): Show |
MOSPD2 | ENSG00000130150.12 | transcript | ENST00000380492.8 | protein_coding | 2/14 | chrX | 14885790 | ||||||
| chrX:14885998
|
G | T | 1 | a0001c0001t0001g0114 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.80-6725G>T | MOSPD2 | ENSG00000130150.12 | transcript | ENST00000380492.8 | protein_coding | 2/14 | chrX | 14885998 | ||||||
| chrX:14886223
|
T | C | 5 | a0001c0001t0002g0003a0001c0001t0002g0012a0001c0001t0002g0031others(2): Show | 10 | HG01106.hp1 HG01891.hp1 HG02109.hp2 others(7): Show |
intron_variant | MODIFIER | c.80-6500T>C | MOSPD2 | ENSG00000130150.12 | transcript | ENST00000380492.8 | protein_coding | 2/14 | chrX | 14886223 | ||||||
| chrX:14886273
|
C | G | 1 | a0001c0001t0001g0157 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.80-6450C>G | MOSPD2 | ENSG00000130150.12 | transcript | ENST00000380492.8 | protein_coding | 2/14 | chrX | 14886273 | ||||||
| chrX:14886487
|
TA | T | 1 | a0001c0001t0001g0113 | 1 | NA19055.hp1 | intron_variant | MODIFIER | c.80-6233delA | MOSPD2 | ENSG00000130150.12 | transcript | ENST00000380492.8 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chrX | 14886487 | |||||
| chrX:14886498
|
T | TACATACA others(3): Show |
4 | a0001c0001t0001g0164a0001c0001t0001g0166a0001c0001t0008g0162others(1): Show | 4 | HG02630.hp1 HG02723.hp1 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.80-6211_80-6202dup others(10): Show |
MOSPD2 | ENSG00000130150.12 | transcript | ENST00000380492.8 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chrX | 14886498 | |||||
| chrX:14886512
|
TAC | T | 2 | a0001c0001t0001g0156a0001c0001t0001g0182 | 2 | HG02965.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.80-6193_80-6192del others(2): Show |
MOSPD2 | ENSG00000130150.12 | transcript | ENST00000380492.8 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chrX | 14886512 | |||||
| chrX:14886546
|
C | CGA | 9 | a0001c0001t0001g0032a0001c0001t0001g0111a0001c0001t0001g0112others(6): Show | 9 | HG00639.hp2 HG00642.hp1 HG01255.hp1 others(6): Show |
intron_variant | MODIFIER | c.80-6152_80-6151dup others(2): Show |
MOSPD2 | ENSG00000130150.12 | transcript | ENST00000380492.8 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chrX | 14886546 | |||||
| chrX:14886546
|
C | CGAGA | 1 | a0001c0001t0001g0132 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.80-6154_80-6151dup others(4): Show |
MOSPD2 | ENSG00000130150.12 | transcript | ENST00000380492.8 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chrX | 14886546 | |||||
| chrX:14886546
|
CGA | C | 1 | a0001c0001t0002g0011 | 2 | HG02970.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.80-6152_80-6151del others(2): Show |
MOSPD2 | ENSG00000130150.12 | transcript | ENST00000380492.8 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chrX | 14886546 | |||||
| chrX:14886546
|
CGAGAGA | C | 1 | a0001c0001t0007g0033 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.80-6156_80-6151del others(6): Show |
MOSPD2 | ENSG00000130150.12 | transcript | ENST00000380492.8 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chrX | 14886546 | |||||
| chrX:14886546
|
CGAGAGAG others(1): Show |
C | 1 | a0001c0001t0001g0038 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.80-6158_80-6151del others(8): Show |
MOSPD2 | ENSG00000130150.12 | transcript | ENST00000380492.8 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chrX | 14886546 | |||||
| chrX:14886546
|
CGAGAGAG others(5): Show |
C | 3 | a0001c0001t0002g0003a0001c0001t0002g0012a0001c0001t0002g0031 | 8 | HG01106.hp1 HG01891.hp1 HG02109.hp2 others(5): Show |
intron_variant | MODIFIER | c.80-6162_80-6151del others(12): Show |
MOSPD2 | ENSG00000130150.12 | transcript | ENST00000380492.8 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chrX | 14886546 | |||||
| chrX:14886549
|
G | A | 1 | a0001c0001t0004g0200 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.80-6174G>A | MOSPD2 | ENSG00000130150.12 | transcript | ENST00000380492.8 | protein_coding | 2/14 | chrX | 14886549 | ||||||
| chrX:14886745
|
C | T | 1 | a0001c0001t0001g0110 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.80-5978C>T | MOSPD2 | ENSG00000130150.12 | transcript | ENST00000380492.8 | protein_coding | 2/14 | chrX | 14886745 | ||||||
| chrX:14886860
|
T | A | 1 | a0001c0001t0001g0134 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.80-5863T>A | MOSPD2 | ENSG00000130150.12 | transcript | ENST00000380492.8 | protein_coding | 2/14 | chrX | 14886860 | ||||||
| chrX:14887267
|
A | G | 1 | a0001c0001t0002g0011 | 2 | HG02970.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.80-5456A>G | MOSPD2 | ENSG00000130150.12 | transcript | ENST00000380492.8 | protein_coding | 2/14 | chrX | 14887267 | ||||||
| chrX:14887359
|
A | C | 1 | a0001c0001t0001g0132 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.80-5364A>C | MOSPD2 | ENSG00000130150.12 | transcript | ENST00000380492.8 | protein_coding | 2/14 | chrX | 14887359 | ||||||
| chrX:14887690
|
T | TACAAC | 11 | a0001c0001t0001g0038a0001c0001t0002g0003a0001c0001t0002g0006others(8): Show | 19 | HG01106.hp1 HG01243.hp1 HG01891.hp1 others(16): Show |
intron_variant | MODIFIER | c.80-5029_80-5028ins others(5): Show |
MOSPD2 | ENSG00000130150.12 | transcript | ENST00000380492.8 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chrX | 14887690 | |||||
| chrX:14887735
|
TGAGA | T | 1 | a0001c0001t0001g0135 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.80-4983_80-4980del others(4): Show |
MOSPD2 | ENSG00000130150.12 | transcript | ENST00000380492.8 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chrX | 14887735 | |||||
| chrX:14887908
|
ATTTG | A | 1 | a0001c0001t0007g0033 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.80-4810_80-4807del others(4): Show |
MOSPD2 | ENSG00000130150.12 | transcript | ENST00000380492.8 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chrX | 14887908 | |||||
| chrX:14888190
|
A | ATG | 11 | a0001c0001t0001g0024a0001c0001t0001g0051a0001c0001t0001g0128others(8): Show | 13 | HG00140.hp1 HG00280.hp1 HG00741.hp1 others(10): Show |
intron_variant | MODIFIER | c.80-4532_80-4531ins others(2): Show |
MOSPD2 | ENSG00000130150.12 | transcript | ENST00000380492.8 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chrX | 14888190 | |||||
| chrX:14888192
|
A | G | 85 | a0001c0001t0001g0004a0001c0001t0001g0010a0001c0001t0001g0025others(82): Show | 99 | HG00408.hp2 HG00423.hp2 HG00558.hp2 others(96): Show |
intron_variant | MODIFIER | c.80-4531A>G | MOSPD2 | ENSG00000130150.12 | transcript | ENST00000380492.8 | protein_coding | 2/14 | chrX | 14888192 | ||||||
| chrX:14888195
|
T | C | 11 | a0001c0001t0001g0024a0001c0001t0001g0051a0001c0001t0001g0128others(8): Show | 13 | HG00140.hp1 HG00280.hp1 HG00741.hp1 others(10): Show |
intron_variant | MODIFIER | c.80-4528T>C | MOSPD2 | ENSG00000130150.12 | transcript | ENST00000380492.8 | protein_coding | 2/14 | chrX | 14888195 | ||||||
| chrX:14888195
|
T | TACAC | 7 | a0001c0001t0001g0138a0001c0001t0001g0139a0001c0001t0001g0140others(4): Show | 7 | HG01175.hp1 HG01891.hp2 HG02735.hp1 others(4): Show |
intron_variant | MODIFIER | c.80-4521_80-4518dup others(4): Show |
MOSPD2 | ENSG00000130150.12 | transcript | ENST00000380492.8 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chrX | 14888195 | |||||
| chrX:14888195
|
T | TACACAC | 1 | a0001c0001t0001g0127 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.80-4523_80-4518dup others(6): Show |
MOSPD2 | ENSG00000130150.12 | transcript | ENST00000380492.8 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chrX | 14888195 | |||||
| chrX:14888195
|
T | TACACACA others(1): Show |
1 | a0001c0001t0001g0043 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.80-4525_80-4518dup others(8): Show |
MOSPD2 | ENSG00000130150.12 | transcript | ENST00000380492.8 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chrX | 14888195 | |||||
| chrX:14888195
|
T | TACACACA others(3): Show |
1 | a0001c0001t0007g0033 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.80-4520_80-4519ins others(10): Show |
MOSPD2 | ENSG00000130150.12 | transcript | ENST00000380492.8 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chrX | 14888195 | |||||
| chrX:14888195
|
T | TATACAC | 1 | a0001c0001t0003g0007 | 3 | HG02293.hp1 HG02622.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.80-4527_80-4526ins others(6): Show |
MOSPD2 | ENSG00000130150.12 | transcript | ENST00000380492.8 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chrX | 14888195 | |||||
| chrX:14888195
|
T | TATACACA others(1): Show |
1 | a0001c0001t0003g0041 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.80-4527_80-4526ins others(8): Show |
MOSPD2 | ENSG00000130150.12 | transcript | ENST00000380492.8 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chrX | 14888195 | |||||
| chrX:14888195
|
TAC | T | 5 | a0001c0001t0001g0019a0001c0001t0001g0119a0001c0001t0001g0120others(2): Show | 6 | HG00741.hp2 HG01361.hp2 HG03669.hp1 others(3): Show |
intron_variant | MODIFIER | c.80-4519_80-4518del others(2): Show |
MOSPD2 | ENSG00000130150.12 | transcript | ENST00000380492.8 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chrX | 14888195 | |||||
| chrX:14888195
|
TACACACA others(5): Show |
T | 2 | a0001c0001t0001g0188a0001c0001t0001g0195 | 2 | HG01081.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.80-4517_80-4506del others(12): Show |
MOSPD2 | ENSG00000130150.12 | transcript | ENST00000380492.8 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chrX | 14888195 | |||||
| chrX:14888195
|
TACACACA others(7): Show |
T | 23 | a0001c0001t0001g0027a0001c0001t0001g0167a0001c0001t0001g0168others(20): Show | 24 | HG00558.hp2 HG00609.hp1 HG00639.hp1 others(21): Show |
intron_variant | MODIFIER | c.80-4517_80-4504del others(14): Show |
MOSPD2 | ENSG00000130150.12 | transcript | ENST00000380492.8 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chrX | 14888195 | |||||
| chrX:14888195
|
TACACACA others(9): Show |
T | 4 | a0001c0001t0001g0038a0001c0001t0001g0154a0001c0001t0001g0155others(1): Show | 4 | HG01070.hp1 HG02723.hp1 HG02723.hp2 others(1): Show |
intron_variant | MODIFIER | c.80-4517_80-4502del others(16): Show |
MOSPD2 | ENSG00000130150.12 | transcript | ENST00000380492.8 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chrX | 14888195 | |||||
| chrX:14888195
|
TACACACA others(13): Show |
T | 6 | a0001c0001t0001g0030a0001c0001t0001g0181a0001c0001t0001g0182others(3): Show | 7 | HG02717.hp1 HG02809.hp1 HG02922.hp1 others(4): Show |
intron_variant | MODIFIER | c.80-4517_80-4498del others(20): Show |
MOSPD2 | ENSG00000130150.12 | transcript | ENST00000380492.8 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chrX | 14888195 | |||||
| chrX:14888195
|
TACACACA others(23): Show |
T | 9 | a0001c0001t0002g0003a0001c0001t0002g0006a0001c0001t0002g0011others(6): Show | 17 | HG01106.hp1 HG01243.hp1 HG01891.hp1 others(14): Show |
intron_variant | MODIFIER | c.80-4517_80-4488del others(30): Show |
MOSPD2 | ENSG00000130150.12 | transcript | ENST00000380492.8 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chrX | 14888195 | |||||
| chrX:14888196
|
A | ACACACAC others(3): Show |
1 | a0001c0001t0001g0058 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.80-4520_80-4519ins others(10): Show |
MOSPD2 | ENSG00000130150.12 | transcript | ENST00000380492.8 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chrX | 14888196 | |||||
| chrX:14888196
|
ACACACAC others(3): Show |
A | 4 | a0001c0001t0001g0131a0001c0001t0001g0153a0001c0001t0001g0159others(1): Show | 4 | HG00423.hp2 HG01109.hp1 NA18967.hp1 others(1): Show |
intron_variant | MODIFIER | c.80-4517_80-4508del others(10): Show |
MOSPD2 | ENSG00000130150.12 | transcript | ENST00000380492.8 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chrX | 14888196 | |||||
| chrX:14888198
|
ACACACAC others(1): Show |
A | 6 | a0001c0001t0001g0047a0001c0001t0001g0161a0001c0001t0001g0164others(3): Show | 6 | HG02056.hp1 HG02523.hp1 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.80-4517_80-4510del others(8): Show |
MOSPD2 | ENSG00000130150.12 | transcript | ENST00000380492.8 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chrX | 14888198 | |||||
| chrX:14888200
|
A | ACACGCG | 1 | a0001c0001t0001g0100 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.80-4520_80-4519ins others(6): Show |
MOSPD2 | ENSG00000130150.12 | transcript | ENST00000380492.8 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chrX | 14888200 | |||||
| chrX:14888200
|
ACACACG | A | 9 | a0001c0001t0001g0004a0001c0001t0001g0046a0001c0001t0001g0134others(6): Show | 12 | HG00408.hp2 HG01433.hp1 HG01928.hp1 others(9): Show |
intron_variant | MODIFIER | c.80-4517_80-4512del others(6): Show |
MOSPD2 | ENSG00000130150.12 | transcript | ENST00000380492.8 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chrX | 14888200 | |||||
| chrX:14888202
|
A | ACGCG | 4 | a0001c0001t0001g0020a0001c0001t0001g0101a0001c0001t0001g0102others(1): Show | 5 | HG00642.hp1 HG01070.hp2 HG01071.hp1 others(2): Show |
intron_variant | MODIFIER | c.80-4520_80-4519ins others(4): Show |
MOSPD2 | ENSG00000130150.12 | transcript | ENST00000380492.8 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chrX | 14888202 | |||||
| chrX:14888202
|
ACACG | A | 10 | a0001c0001t0001g0010a0001c0001t0001g0032a0001c0001t0001g0052others(7): Show | 12 | HG00733.hp2 HG01975.hp1 HG02148.hp1 others(9): Show |
intron_variant | MODIFIER | c.80-4517_80-4514del others(4): Show |
MOSPD2 | ENSG00000130150.12 | transcript | ENST00000380492.8 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chrX | 14888202 | |||||
| chrX:14888204
|
A | G | 25 | a0001c0001t0001g0015a0001c0001t0001g0016a0001c0001t0001g0017others(22): Show | 33 | HG00408.hp1 HG00423.hp1 HG00621.hp1 others(30): Show |
intron_variant | MODIFIER | c.80-4519A>G | MOSPD2 | ENSG00000130150.12 | transcript | ENST00000380492.8 | protein_coding | 2/14 | chrX | 14888204 | ||||||
| chrX:14888204
|
ACG | A | 9 | a0001c0001t0001g0025a0001c0001t0001g0045a0001c0001t0001g0144others(6): Show | 11 | HG01069.hp1 HG01071.hp2 HG01256.hp1 others(8): Show |
intron_variant | MODIFIER | c.80-4517_80-4516del others(2): Show |
MOSPD2 | ENSG00000130150.12 | transcript | ENST00000380492.8 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chrX | 14888204 | |||||
| chrX:14888206
|
G | A | 35 | a0001c0001t0001g0020a0001c0001t0001g0024a0001c0001t0001g0043others(32): Show | 43 | HG00140.hp1 HG00280.hp1 HG00642.hp1 others(40): Show |
intron_variant | MODIFIER | c.80-4517G>A | MOSPD2 | ENSG00000130150.12 | transcript | ENST00000380492.8 | protein_coding | 2/14 | chrX | 14888206 | ||||||
| chrX:14888206
|
G | GCA | 22 | a0001c0001t0001g0002a0001c0001t0001g0013a0001c0001t0001g0015others(19): Show | 33 | HG00408.hp1 HG00423.hp1 HG00558.hp1 others(30): Show |
intron_variant | MODIFIER | c.80-4475_80-4474dup others(2): Show |
MOSPD2 | ENSG00000130150.12 | transcript | ENST00000380492.8 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chrX | 14888206 | |||||
| chrX:14888206
|
G | GCACA | 1 | a0001c0001t0001g0070 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.80-4477_80-4474dup others(4): Show |
MOSPD2 | ENSG00000130150.12 | transcript | ENST00000380492.8 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chrX | 14888206 | |||||
| chrX:14888206
|
G | GCACACA | 1 | a0001c0001t0001g0069 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.80-4479_80-4474dup others(6): Show |
MOSPD2 | ENSG00000130150.12 | transcript | ENST00000380492.8 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chrX | 14888206 | |||||
| chrX:14888206
|
GCA | G | 5 | a0001c0001t0001g0095a0001c0001t0001g0096a0001c0001t0001g0097others(2): Show | 5 | HG02027.hp1 HG03490.hp1 HG04184.hp2 others(2): Show |
intron_variant | MODIFIER | c.80-4475_80-4474del others(2): Show |
MOSPD2 | ENSG00000130150.12 | transcript | ENST00000380492.8 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chrX | 14888206 | |||||
| chrX:14888206
|
GCACA | G | 3 | a0001c0001t0001g0099a0001c0001t0001g0122a0001c0001t0001g0133 | 3 | HG02615.hp1 NA19030.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.80-4477_80-4474del others(4): Show |
MOSPD2 | ENSG00000130150.12 | transcript | ENST00000380492.8 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chrX | 14888206 | |||||
| chrX:14888206
|
GCACACA | G | 1 | a0001c0001t0001g0022 | 2 | HG03195.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.80-4479_80-4474del others(6): Show |
MOSPD2 | ENSG00000130150.12 | transcript | ENST00000380492.8 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chrX | 14888206 | |||||
| chrX:14888206
|
GCACACAC others(1): Show |
G | 1 | a0001c0001t0001g0054 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.80-4481_80-4474del others(8): Show |
MOSPD2 | ENSG00000130150.12 | transcript | ENST00000380492.8 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chrX | 14888206 | |||||
| chrX:14888208
|
A | G | 5 | a0001c0001t0001g0019a0001c0001t0001g0119a0001c0001t0001g0120others(2): Show | 6 | HG00741.hp2 HG01361.hp2 HG03669.hp1 others(3): Show |
intron_variant | MODIFIER | c.80-4515A>G | MOSPD2 | ENSG00000130150.12 | transcript | ENST00000380492.8 | protein_coding | 2/14 | chrX | 14888208 | ||||||
| chrX:14888210
|
A | G | 3 | a0001c0001t0001g0164a0001c0001t0008g0162a0001c0004t0001g0165 | 3 | HG02630.hp1 HG02886.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.80-4513A>G | MOSPD2 | ENSG00000130150.12 | transcript | ENST00000380492.8 | protein_coding | 2/14 | chrX | 14888210 | ||||||
| chrX:14888212
|
A | G | 3 | a0001c0001t0001g0164a0001c0001t0008g0162a0001c0004t0001g0165 | 3 | HG02630.hp1 HG02886.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.80-4511A>G | MOSPD2 | ENSG00000130150.12 | transcript | ENST00000380492.8 | protein_coding | 2/14 | chrX | 14888212 | ||||||
| chrX:14888218
|
A | G | 1 | a0001c0001t0001g0166 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.80-4505A>G | MOSPD2 | ENSG00000130150.12 | transcript | ENST00000380492.8 | protein_coding | 2/14 | chrX | 14888218 | ||||||
| chrX:14888220
|
A | G | 2 | a0001c0001t0001g0038a0001c0001t0001g0166 | 2 | HG02723.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.80-4503A>G | MOSPD2 | ENSG00000130150.12 | transcript | ENST00000380492.8 | protein_coding | 2/14 | chrX | 14888220 | ||||||
| chrX:14888234
|
A | G | 9 | a0001c0001t0002g0003a0001c0001t0002g0006a0001c0001t0002g0011others(6): Show | 17 | HG01106.hp1 HG01243.hp1 HG01891.hp1 others(14): Show |
intron_variant | MODIFIER | c.80-4489A>G | MOSPD2 | ENSG00000130150.12 | transcript | ENST00000380492.8 | protein_coding | 2/14 | chrX | 14888234 | ||||||
| chrX:14888249
|
C | CA | 1 | a0001c0001t0001g0049 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.80-4474_80-4473ins others(1): Show |
MOSPD2 | ENSG00000130150.12 | transcript | ENST00000380492.8 | protein_coding | 2/14 | chrX | 14888249 | ||||||
| chrX:14888299
|
C | G | 3 | a0001c0001t0002g0006a0001c0001t0002g0039a0001c0001t0002g0040 | 5 | HG01243.hp1 HG02280.hp1 HG02622.hp2 others(2): Show |
intron_variant | MODIFIER | c.80-4424C>G | MOSPD2 | ENSG00000130150.12 | transcript | ENST00000380492.8 | protein_coding | 2/14 | chrX | 14888299 | ||||||
| chrX:14888394
|
C | T | 1 | a0001c0001t0002g0011 | 2 | HG02970.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.80-4329C>T | MOSPD2 | ENSG00000130150.12 | transcript | ENST00000380492.8 | protein_coding | 2/14 | chrX | 14888394 | ||||||
| chrX:14888435
|
C | G | 112 | a0001c0001t0001g0004a0001c0001t0001g0010a0001c0001t0001g0024others(109): Show | 136 | HG00140.hp1 HG00280.hp1 HG00408.hp2 others(133): Show |
intron_variant | MODIFIER | c.80-4288C>G | MOSPD2 | ENSG00000130150.12 | transcript | ENST00000380492.8 | protein_coding | 2/14 | chrX | 14888435 | ||||||
| chrX:14888477
|
C | T | 2 | a0001c0001t0001g0179a0001c0001t0001g0180 | 2 | HG01358.hp1 HG01981.hp1 |
intron_variant | MODIFIER | c.80-4246C>T | MOSPD2 | ENSG00000130150.12 | transcript | ENST00000380492.8 | protein_coding | 2/14 | chrX | 14888477 | ||||||
| chrX:14888567
|
A | G | 1 | a0001c0001t0001g0094 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.80-4156A>G | MOSPD2 | ENSG00000130150.12 | transcript | ENST00000380492.8 | protein_coding | 2/14 | chrX | 14888567 | ||||||
| chrX:14888759
|
A | G | 1 | a0001c0001t0001g0038 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.80-3964A>G | MOSPD2 | ENSG00000130150.12 | transcript | ENST00000380492.8 | protein_coding | 2/14 | chrX | 14888759 | ||||||
| chrX:14888760
|
G | GGTGT | 1 | a0001c0001t0001g0038 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.80-3962_80-3961ins others(4): Show |
MOSPD2 | ENSG00000130150.12 | transcript | ENST00000380492.8 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chrX | 14888760 | |||||
| chrX:14888762
|
G | GGT | 9 | a0001c0001t0002g0003a0001c0001t0002g0006a0001c0001t0002g0011others(6): Show | 17 | HG01106.hp1 HG01243.hp1 HG01891.hp1 others(14): Show |
intron_variant | MODIFIER | c.80-3940_80-3939dup others(2): Show |
MOSPD2 | ENSG00000130150.12 | transcript | ENST00000380492.8 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chrX | 14888762 | |||||
| chrX:14888762
|
G | GGTGTGT | 1 | a0001c0001t0007g0033 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.80-3944_80-3939dup others(6): Show |
MOSPD2 | ENSG00000130150.12 | transcript | ENST00000380492.8 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chrX | 14888762 | |||||
| chrX:14888762
|
G | GT | 1 | a0001c0001t0001g0117 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.80-3961_80-3960ins others(1): Show |
MOSPD2 | ENSG00000130150.12 | transcript | ENST00000380492.8 | protein_coding | 2/14 | chrX | 14888762 | ||||||
| chrX:14888762
|
G | T | 1 | a0001c0001t0001g0038 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.80-3961G>T | MOSPD2 | ENSG00000130150.12 | transcript | ENST00000380492.8 | protein_coding | 2/14 | chrX | 14888762 | ||||||
| chrX:14888784
|
T | TG | 1 | a0001c0001t0003g0185 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.80-3939_80-3938ins others(1): Show |
MOSPD2 | ENSG00000130150.12 | transcript | ENST00000380492.8 | protein_coding | 2/14 | chrX | 14888784 | ||||||
| chrX:14888789
|
G | A | 1 | a0001c0001t0001g0154 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.80-3934G>A | MOSPD2 | ENSG00000130150.12 | transcript | ENST00000380492.8 | protein_coding | 2/14 | chrX | 14888789 | ||||||
| chrX:14888823
|
T | C | 112 | a0001c0001t0001g0004a0001c0001t0001g0010a0001c0001t0001g0024others(109): Show | 136 | HG00140.hp1 HG00280.hp1 HG00408.hp2 others(133): Show |
intron_variant | MODIFIER | c.80-3900T>C | MOSPD2 | ENSG00000130150.12 | transcript | ENST00000380492.8 | protein_coding | 2/14 | chrX | 14888823 | ||||||
| chrX:14888844
|
G | A | 4 | a0001c0001t0001g0164a0001c0001t0001g0166a0001c0001t0008g0162others(1): Show | 4 | HG02630.hp1 HG02723.hp1 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.80-3879G>A | MOSPD2 | ENSG00000130150.12 | transcript | ENST00000380492.8 | protein_coding | 2/14 | chrX | 14888844 | ||||||
| chrX:14889303
|
A | G | 1 | a0001c0001t0001g0038 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.80-3420A>G | MOSPD2 | ENSG00000130150.12 | transcript | ENST00000380492.8 | protein_coding | 2/14 | chrX | 14889303 | ||||||
| chrX:14889315
|
G | A | 1 | a0001c0001t0001g0038 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.80-3408G>A | MOSPD2 | ENSG00000130150.12 | transcript | ENST00000380492.8 | protein_coding | 2/14 | chrX | 14889315 | ||||||
| chrX:14889467
|
T | C | 1 | a0001c0001t0001g0038 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.80-3256T>C | MOSPD2 | ENSG00000130150.12 | transcript | ENST00000380492.8 | protein_coding | 2/14 | chrX | 14889467 | ||||||
| chrX:14889716
|
G | A | 1 | a0001c0001t0001g0182 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.80-3007G>A | MOSPD2 | ENSG00000130150.12 | transcript | ENST00000380492.8 | protein_coding | 2/14 | chrX | 14889716 | ||||||
| chrX:14889760
|
T | G | 1 | a0001c0001t0001g0038 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.80-2963T>G | MOSPD2 | ENSG00000130150.12 | transcript | ENST00000380492.8 | protein_coding | 2/14 | chrX | 14889760 | ||||||
| chrX:14889824
|
TG | T | 1 | a0001c0001t0007g0033 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.80-2897delG | MOSPD2 | ENSG00000130150.12 | transcript | ENST00000380492.8 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chrX | 14889824 | |||||
| chrX:14889954
|
A | G | 5 | a0001c0001t0001g0009a0001c0001t0001g0013a0001c0001t0001g0091others(2): Show | 8 | HG00558.hp1 HG02080.hp1 NA18944.hp1 others(5): Show |
intron_variant | MODIFIER | c.80-2769A>G | MOSPD2 | ENSG00000130150.12 | transcript | ENST00000380492.8 | protein_coding | 2/14 | chrX | 14889954 | ||||||
| chrX:14890195
|
T | TA | 15 | a0001c0001t0001g0038a0001c0001t0001g0127a0001c0001t0001g0128others(12): Show | 23 | HG01106.hp1 HG01109.hp1 HG01243.hp1 others(20): Show |
intron_variant | MODIFIER | c.80-2517dupA | MOSPD2 | ENSG00000130150.12 | transcript | ENST00000380492.8 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chrX | 14890195 | |||||
| chrX:14890195
|
TA | T | 1 | a0001c0001t0001g0118 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.80-2517delA | MOSPD2 | ENSG00000130150.12 | transcript | ENST00000380492.8 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chrX | 14890195 | |||||
| chrX:14890303
|
C | G | 1 | a0001c0001t0001g0155 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.80-2420C>G | MOSPD2 | ENSG00000130150.12 | transcript | ENST00000380492.8 | protein_coding | 2/14 | chrX | 14890303 | ||||||
| chrX:14890469
|
A | T | 1 | a0001c0001t0001g0055 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.80-2254A>T | MOSPD2 | ENSG00000130150.12 | transcript | ENST00000380492.8 | protein_coding | 2/14 | chrX | 14890469 | ||||||
| chrX:14890551
|
T | TA | 4 | a0001c0001t0001g0164a0001c0001t0001g0166a0001c0001t0008g0162others(1): Show | 4 | HG02630.hp1 HG02723.hp1 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.80-2171dupA | MOSPD2 | ENSG00000130150.12 | transcript | ENST00000380492.8 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chrX | 14890551 | |||||
| chrX:14890915
|
C | G | 1 | a0001c0001t0001g0181 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.80-1808C>G | MOSPD2 | ENSG00000130150.12 | transcript | ENST00000380492.8 | protein_coding | 2/14 | chrX | 14890915 | ||||||
| chrX:14891362
|
T | C | 4 | a0001c0001t0001g0164a0001c0001t0001g0166a0001c0001t0008g0162others(1): Show | 4 | HG02630.hp1 HG02723.hp1 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.80-1361T>C | MOSPD2 | ENSG00000130150.12 | transcript | ENST00000380492.8 | protein_coding | 2/14 | chrX | 14891362 | ||||||
| chrX:14891436
|
A | G | 1 | a0001c0001t0001g0038 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.80-1287A>G | MOSPD2 | ENSG00000130150.12 | transcript | ENST00000380492.8 | protein_coding | 2/14 | chrX | 14891436 | ||||||
| chrX:14891500
|
AT | A | 2 | a0001c0001t0001g0130a0001c0001t0001g0179 | 2 | HG01981.hp1 NA18962.hp1 |
intron_variant | MODIFIER | c.80-1213delT | MOSPD2 | ENSG00000130150.12 | transcript | ENST00000380492.8 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chrX | 14891500 | |||||
| chrX:14891525
|
T | A | 1 | a0001c0001t0001g0189 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.80-1198T>A | MOSPD2 | ENSG00000130150.12 | transcript | ENST00000380492.8 | protein_coding | 2/14 | chrX | 14891525 | ||||||
| chrX:14891568
|
A | T | 112 | a0001c0001t0001g0004a0001c0001t0001g0010a0001c0001t0001g0024others(109): Show | 136 | HG00140.hp1 HG00280.hp1 HG00408.hp2 others(133): Show |
intron_variant | MODIFIER | c.80-1155A>T | MOSPD2 | ENSG00000130150.12 | transcript | ENST00000380492.8 | protein_coding | 2/14 | chrX | 14891568 | ||||||
| chrX:14891580
|
T | A | 3 | a0001c0001t0001g0057a0001c0001t0001g0067a0001c0001t0001g0107 | 3 | HG00735.hp2 HG02602.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.80-1143T>A | MOSPD2 | ENSG00000130150.12 | transcript | ENST00000380492.8 | protein_coding | 2/14 | chrX | 14891580 | ||||||
| chrX:14891660
|
C | T | 97 | a0001c0001t0001g0004a0001c0001t0001g0010a0001c0001t0001g0024others(94): Show | 113 | HG00140.hp1 HG00280.hp1 HG00408.hp2 others(110): Show |
intron_variant | MODIFIER | c.80-1063C>T | MOSPD2 | ENSG00000130150.12 | transcript | ENST00000380492.8 | protein_coding | 2/14 | chrX | 14891660 | ||||||
| chrX:14891813
|
T | C | 1 | a0001c0001t0001g0038 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.80-910T>C | MOSPD2 | ENSG00000130150.12 | transcript | ENST00000380492.8 | protein_coding | 2/14 | chrX | 14891813 | ||||||
| chrX:14891823
|
TC | T | 1 | a0001c0001t0001g0108 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.80-897delC | MOSPD2 | ENSG00000130150.12 | transcript | ENST00000380492.8 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chrX | 14891823 | |||||
| chrX:14891862
|
T | C | 1 | a0001c0001t0001g0103 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.80-861T>C | MOSPD2 | ENSG00000130150.12 | transcript | ENST00000380492.8 | protein_coding | 2/14 | chrX | 14891862 | ||||||
| chrX:14891925
|
G | A | 2 | a0001c0001t0001g0071a0001c0001t0001g0078 | 2 | NA19075.hp1 NA19086.hp1 |
intron_variant | MODIFIER | c.80-798G>A | MOSPD2 | ENSG00000130150.12 | transcript | ENST00000380492.8 | protein_coding | 2/14 | chrX | 14891925 | ||||||
| chrX:14892105
|
T | A | 1 | a0001c0001t0001g0141 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.80-618T>A | MOSPD2 | ENSG00000130150.12 | transcript | ENST00000380492.8 | protein_coding | 2/14 | chrX | 14892105 | ||||||
| chrX:14892252
|
T | A | 1 | a0001c0001t0007g0033 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.80-471T>A | MOSPD2 | ENSG00000130150.12 | transcript | ENST00000380492.8 | protein_coding | 2/14 | chrX | 14892252 | ||||||
| chrX:14892385
|
G | A | 1 | a0001c0001t0001g0038 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.80-338G>A | MOSPD2 | ENSG00000130150.12 | transcript | ENST00000380492.8 | protein_coding | 2/14 | chrX | 14892385 | ||||||
| chrX:14892389
|
G | A | 1 | a0001c0001t0001g0196 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.80-334G>A | MOSPD2 | ENSG00000130150.12 | transcript | ENST00000380492.8 | protein_coding | 2/14 | chrX | 14892389 | ||||||
| chrX:14892576
|
T | G | 1 | a0001c0001t0007g0033 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.80-147T>G | MOSPD2 | ENSG00000130150.12 | transcript | ENST00000380492.8 | protein_coding | 2/14 | chrX | 14892576 | ||||||
| chrX:14893248
|
C | A | 9 | a0001c0001t0002g0003a0001c0001t0002g0006a0001c0001t0002g0011others(6): Show | 17 | HG01106.hp1 HG01243.hp1 HG01891.hp1 others(14): Show |
intron_variant | MODIFIER | c.235+370C>A | MOSPD2 | ENSG00000130150.12 | transcript | ENST00000380492.8 | protein_coding | 3/14 | chrX | 14893248 | ||||||
| chrX:14893525
|
A | G | 1 | a0001c0001t0001g0158 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.235+647A>G | MOSPD2 | ENSG00000130150.12 | transcript | ENST00000380492.8 | protein_coding | 3/14 | chrX | 14893525 | ||||||
| chrX:14893749
|
AT | A | 2 | a0001c0001t0001g0020a0001c0001t0001g0021 | 4 | HG01070.hp2 HG01071.hp1 HG02257.hp1 others(1): Show |
intron_variant | MODIFIER | c.235+872delT | MOSPD2 | ENSG00000130150.12 | transcript | ENST00000380492.8 | protein_coding | 3/14 | chrX | 14893749 | ||||||
| chrX:14893845
|
T | G | 1 | a0001c0001t0007g0033 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.235+967T>G | MOSPD2 | ENSG00000130150.12 | transcript | ENST00000380492.8 | protein_coding | 3/14 | chrX | 14893845 | ||||||
| chrX:14893888
|
T | G | 3 | a0001c0001t0002g0003a0001c0001t0002g0012a0001c0001t0002g0031 | 8 | HG01106.hp1 HG01891.hp1 HG02109.hp2 others(5): Show |
intron_variant | MODIFIER | c.235+1010T>G | MOSPD2 | ENSG00000130150.12 | transcript | ENST00000380492.8 | protein_coding | 3/14 | chrX | 14893888 | ||||||
| chrX:14893907
|
C | T | 124 | a0001c0001t0001g0004a0001c0001t0001g0010a0001c0001t0001g0022others(121): Show | 151 | HG00140.hp1 HG00280.hp1 HG00408.hp2 others(148): Show |
intron_variant | MODIFIER | c.235+1029C>T | MOSPD2 | ENSG00000130150.12 | transcript | ENST00000380492.8 | protein_coding | 3/14 | chrX | 14893907 | ||||||
| chrX:14894300
|
A | T | 13 | a0001c0001t0001g0038a0001c0001t0001g0164a0001c0001t0001g0166others(10): Show | 21 | HG01106.hp1 HG01243.hp1 HG01891.hp1 others(18): Show |
intron_variant | MODIFIER | c.236-1008A>T | MOSPD2 | ENSG00000130150.12 | transcript | ENST00000380492.8 | protein_coding | 3/14 | chrX | 14894300 | ||||||
| chrX:14894316
|
A | AT | 24 | a0001c0001t0001g0025a0001c0001t0001g0030a0001c0001t0001g0047others(21): Show | 30 | HG00733.hp2 HG01069.hp1 HG01070.hp1 others(27): Show |
intron_variant | MODIFIER | c.236-973dupT | MOSPD2 | ENSG00000130150.12 | transcript | ENST00000380492.8 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chrX | 14894316 | |||||
| chrX:14894316
|
A | ATT | 46 | a0001c0001t0001g0004a0001c0001t0001g0010a0001c0001t0001g0024others(43): Show | 53 | HG00140.hp1 HG00280.hp1 HG00408.hp2 others(50): Show |
intron_variant | MODIFIER | c.236-974_236-973dup others(2): Show |
MOSPD2 | ENSG00000130150.12 | transcript | ENST00000380492.8 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chrX | 14894316 | |||||
| chrX:14894316
|
A | ATTT | 5 | a0001c0001t0001g0051a0001c0001t0001g0135a0001c0001t0001g0163others(2): Show | 5 | HG01433.hp1 HG02723.hp1 HG02886.hp1 others(2): Show |
intron_variant | MODIFIER | c.236-975_236-973dup others(3): Show |
MOSPD2 | ENSG00000130150.12 | transcript | ENST00000380492.8 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chrX | 14894316 | |||||
| chrX:14894316
|
AT | A | 19 | a0001c0001t0001g0020a0001c0001t0001g0022a0001c0001t0001g0038others(16): Show | 22 | HG01070.hp2 HG01071.hp1 HG01257.hp1 others(19): Show |
intron_variant | MODIFIER | c.236-973delT | MOSPD2 | ENSG00000130150.12 | transcript | ENST00000380492.8 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chrX | 14894316 | |||||
| chrX:14894316
|
ATT | A | 4 | a0001c0001t0002g0006a0001c0001t0002g0039a0001c0001t0002g0040others(1): Show | 6 | HG01175.hp2 HG01243.hp1 HG02280.hp1 others(3): Show |
intron_variant | MODIFIER | c.236-974_236-973del others(2): Show |
MOSPD2 | ENSG00000130150.12 | transcript | ENST00000380492.8 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chrX | 14894316 | |||||
| chrX:14894336
|
G | A | 1 | a0001c0001t0010g0104 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.236-972G>A | MOSPD2 | ENSG00000130150.12 | transcript | ENST00000380492.8 | protein_coding | 3/14 | chrX | 14894336 | ||||||
| chrX:14894387
|
G | T | 9 | a0001c0001t0002g0003a0001c0001t0002g0006a0001c0001t0002g0011others(6): Show | 17 | HG01106.hp1 HG01243.hp1 HG01891.hp1 others(14): Show |
intron_variant | MODIFIER | c.236-921G>T | MOSPD2 | ENSG00000130150.12 | transcript | ENST00000380492.8 | protein_coding | 3/14 | chrX | 14894387 | ||||||
| chrX:14894417
|
C | T | 1 | a0001c0001t0008g0162 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.236-891C>T | MOSPD2 | ENSG00000130150.12 | transcript | ENST00000380492.8 | protein_coding | 3/14 | chrX | 14894417 | ||||||
| chrX:14894436
|
C | A | 1 | a0001c0001t0001g0044 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.236-872C>A | MOSPD2 | ENSG00000130150.12 | transcript | ENST00000380492.8 | protein_coding | 3/14 | chrX | 14894436 | ||||||
| chrX:14894565
|
C | T | 13 | a0001c0001t0001g0038a0001c0001t0001g0164a0001c0001t0001g0166others(10): Show | 21 | HG01106.hp1 HG01243.hp1 HG01891.hp1 others(18): Show |
intron_variant | MODIFIER | c.236-743C>T | MOSPD2 | ENSG00000130150.12 | transcript | ENST00000380492.8 | protein_coding | 3/14 | chrX | 14894565 | ||||||
| chrX:14894665
|
C | T | 1 | a0001c0001t0001g0076 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.236-643C>T | MOSPD2 | ENSG00000130150.12 | transcript | ENST00000380492.8 | protein_coding | 3/14 | chrX | 14894665 | ||||||
| chrX:14894676
|
C | T | 1 | a0001c0001t0001g0178 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.236-632C>T | MOSPD2 | ENSG00000130150.12 | transcript | ENST00000380492.8 | protein_coding | 3/14 | chrX | 14894676 | ||||||
| chrX:14894704
|
G | A | 1 | a0001c0001t0001g0038 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.236-604G>A | MOSPD2 | ENSG00000130150.12 | transcript | ENST00000380492.8 | protein_coding | 3/14 | chrX | 14894704 | ||||||
| chrX:14894987
|
G | T | 3 | a0001c0001t0001g0195a0001c0001t0001g0196a0001c0001t0001g0197 | 3 | HG03041.hp1 HG06807.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.236-321G>T | MOSPD2 | ENSG00000130150.12 | transcript | ENST00000380492.8 | protein_coding | 3/14 | chrX | 14894987 | ||||||
| chrX:14895081
|
T | C | 1 | a0001c0001t0001g0138 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.236-227T>C | MOSPD2 | ENSG00000130150.12 | transcript | ENST00000380492.8 | protein_coding | 3/14 | chrX | 14895081 | ||||||
| chrX:14895087
|
G | A | 1 | a0001c0001t0001g0167 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.236-221G>A | MOSPD2 | ENSG00000130150.12 | transcript | ENST00000380492.8 | protein_coding | 3/14 | chrX | 14895087 | ||||||
| chrX:14895127
|
TTTAG | T | 1 | a0001c0001t0002g0204 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.236-178_236-175del others(4): Show |
MOSPD2 | ENSG00000130150.12 | transcript | ENST00000380492.8 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chrX | 14895127 | |||||
| chrX:14895214
|
G | A | 4 | a0001c0001t0001g0043a0001c0001t0001g0044a0001c0001t0001g0045others(1): Show | 4 | HG03139.hp1 HG03516.hp2 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.236-94G>A | MOSPD2 | ENSG00000130150.12 | transcript | ENST00000380492.8 | protein_coding | 3/14 | chrX | 14895214 | ||||||
| chrX:14895437
|
G | A | 1 | a0001c0001t0001g0150 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.322+43G>A | MOSPD2 | ENSG00000130150.12 | transcript | ENST00000380492.8 | protein_coding | 4/14 | chrX | 14895437 | ||||||
| chrX:14895475
|
G | A | 1 | a0001c0001t0001g0060 | 1 | NA19074.hp1 | intron_variant | MODIFIER | c.322+81G>A | MOSPD2 | ENSG00000130150.12 | transcript | ENST00000380492.8 | protein_coding | 4/14 | chrX | 14895475 | ||||||
| chrX:14895670
|
C | G | 1 | a0001c0001t0007g0033 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.322+276C>G | MOSPD2 | ENSG00000130150.12 | transcript | ENST00000380492.8 | protein_coding | 4/14 | chrX | 14895670 | ||||||
| chrX:14895696
|
G | A | 113 | a0001c0001t0001g0004a0001c0001t0001g0010a0001c0001t0001g0024others(110): Show | 137 | HG00140.hp1 HG00280.hp1 HG00408.hp2 others(134): Show |
intron_variant | MODIFIER | c.322+302G>A | MOSPD2 | ENSG00000130150.12 | transcript | ENST00000380492.8 | protein_coding | 4/14 | chrX | 14895696 | ||||||
| chrX:14895848
|
A | G | 9 | a0001c0001t0002g0003a0001c0001t0002g0006a0001c0001t0002g0011others(6): Show | 17 | HG01106.hp1 HG01243.hp1 HG01891.hp1 others(14): Show |
intron_variant | MODIFIER | c.322+454A>G | MOSPD2 | ENSG00000130150.12 | transcript | ENST00000380492.8 | protein_coding | 4/14 | chrX | 14895848 | ||||||
| chrX:14895982
|
A | G | 1 | a0001c0001t0001g0182 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.322+588A>G | MOSPD2 | ENSG00000130150.12 | transcript | ENST00000380492.8 | protein_coding | 4/14 | chrX | 14895982 | ||||||
| chrX:14896527
|
G | A | 5 | a0001c0001t0002g0003a0001c0001t0002g0012a0001c0001t0002g0031others(2): Show | 10 | HG01106.hp1 HG01891.hp1 HG02109.hp2 others(7): Show |
intron_variant | MODIFIER | c.323-557G>A | MOSPD2 | ENSG00000130150.12 | transcript | ENST00000380492.8 | protein_coding | 4/14 | chrX | 14896527 | ||||||
| chrX:14897450
|
G | A | 1 | a0001c0001t0001g0110 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.477+212G>A | MOSPD2 | ENSG00000130150.12 | transcript | ENST00000380492.8 | protein_coding | 5/14 | chrX | 14897450 | ||||||
| chrX:14897743
|
A | T | 2 | a0001c0001t0001g0089a0001c0001t0012g0088 | 2 | HG01192.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.477+505A>T | MOSPD2 | ENSG00000130150.12 | transcript | ENST00000380492.8 | protein_coding | 5/14 | chrX | 14897743 | ||||||
| chrX:14898340
|
A | G | 30 | a0001c0001t0001g0027a0001c0001t0001g0099a0001c0001t0001g0167others(27): Show | 31 | HG00558.hp2 HG00609.hp1 HG00639.hp1 others(28): Show |
intron_variant | MODIFIER | c.477+1102A>G | MOSPD2 | ENSG00000130150.12 | transcript | ENST00000380492.8 | protein_coding | 5/14 | chrX | 14898340 | ||||||
| chrX:14898404
|
A | G | 1 | a0001c0001t0001g0181 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.477+1166A>G | MOSPD2 | ENSG00000130150.12 | transcript | ENST00000380492.8 | protein_coding | 5/14 | chrX | 14898404 | ||||||
| chrX:14898405
|
T | TAACA | 114 | a0001c0001t0001g0004a0001c0001t0001g0010a0001c0001t0001g0024others(111): Show | 138 | HG00140.hp1 HG00280.hp1 HG00408.hp2 others(135): Show |
intron_variant | MODIFIER | c.477+1168_477+1171d others(6): Show |
MOSPD2 | ENSG00000130150.12 | transcript | ENST00000380492.8 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chrX | 14898405 | |||||
| chrX:14898406
|
A | AAC | 1 | a0001c0001t0001g0115 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.477+1172_477+1173d others(4): Show |
MOSPD2 | ENSG00000130150.12 | transcript | ENST00000380492.8 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chrX | 14898406 | |||||
| chrX:14898513
|
T | C | 3 | a0001c0001t0004g0200a0001c0001t0004g0201a0001c0001t0004g0202 | 3 | HG02809.hp1 HG02922.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.477+1275T>C | MOSPD2 | ENSG00000130150.12 | transcript | ENST00000380492.8 | protein_coding | 5/14 | chrX | 14898513 | ||||||
| chrX:14898636
|
C | A | 14 | a0001c0001t0001g0038a0001c0001t0001g0164a0001c0001t0001g0166others(11): Show | 22 | HG01106.hp1 HG01243.hp1 HG01891.hp1 others(19): Show |
intron_variant | MODIFIER | c.477+1398C>A | MOSPD2 | ENSG00000130150.12 | transcript | ENST00000380492.8 | protein_coding | 5/14 | chrX | 14898636 | ||||||
| chrX:14899064
|
C | T | 27 | a0001c0001t0001g0027a0001c0001t0001g0099a0001c0001t0001g0167others(24): Show | 28 | HG00558.hp2 HG00609.hp1 HG00639.hp1 others(25): Show |
intron_variant | MODIFIER | c.478-1511C>T | MOSPD2 | ENSG00000130150.12 | transcript | ENST00000380492.8 | protein_coding | 5/14 | chrX | 14899064 | ||||||
| chrX:14899114
|
T | TGAACTAG others(299): Show |
1 | a0001c0001t0001g0181 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.478-1444_478-1443i others(308): Show |
MOSPD2 | ENSG00000130150.12 | transcript | ENST00000380492.8 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chrX | 14899114 | |||||
| chrX:14899114
|
T | TGAACTAG others(302): Show |
1 | a0001c0001t0001g0027 | 2 | HG01257.hp2 HG01258.hp1 |
intron_variant | MODIFIER | c.478-1444_478-1443i others(311): Show |
MOSPD2 | ENSG00000130150.12 | transcript | ENST00000380492.8 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chrX | 14899114 | |||||
| chrX:14899114
|
T | TGAACTAG others(308): Show |
1 | a0001c0001t0001g0188 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.478-1444_478-1443i others(317): Show |
MOSPD2 | ENSG00000130150.12 | transcript | ENST00000380492.8 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chrX | 14899114 | |||||
| chrX:14899114
|
T | TGAACTAG others(309): Show |
1 | a0001c0001t0001g0168 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.478-1444_478-1443i others(318): Show |
MOSPD2 | ENSG00000130150.12 | transcript | ENST00000380492.8 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chrX | 14899114 | |||||
| chrX:14899114
|
T | TGAACTAG others(311): Show |
1 | a0001c0001t0001g0169 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.478-1444_478-1443i others(320): Show |
MOSPD2 | ENSG00000130150.12 | transcript | ENST00000380492.8 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chrX | 14899114 | |||||
| chrX:14899114
|
T | TGAACTAG others(314): Show |
2 | a0001c0001t0001g0190a0001c0001t0001g0191 | 2 | HG01496.hp2 HG01516.hp1 |
intron_variant | MODIFIER | c.478-1444_478-1443i others(323): Show |
MOSPD2 | ENSG00000130150.12 | transcript | ENST00000380492.8 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chrX | 14899114 | |||||
| chrX:14899114
|
T | TGAACTAG others(316): Show |
1 | a0001c0001t0001g0206 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.478-1444_478-1443i others(325): Show |
MOSPD2 | ENSG00000130150.12 | transcript | ENST00000380492.8 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chrX | 14899114 | |||||
| chrX:14899114
|
T | TGAACTAG others(318): Show |
1 | a0001c0001t0001g0182 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.478-1444_478-1443i others(327): Show |
MOSPD2 | ENSG00000130150.12 | transcript | ENST00000380492.8 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chrX | 14899114 | |||||
| chrX:14899114
|
T | TGAACTAG others(320): Show |
1 | a0001c0001t0001g0170 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.478-1444_478-1443i others(329): Show |
MOSPD2 | ENSG00000130150.12 | transcript | ENST00000380492.8 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chrX | 14899114 | |||||
| chrX:14899114
|
T | TGAACTAG others(331): Show |
1 | a0001c0001t0001g0099 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.478-1444_478-1443i others(340): Show |
MOSPD2 | ENSG00000130150.12 | transcript | ENST00000380492.8 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chrX | 14899114 | |||||
| chrX:14899114
|
T | TGAACTAG others(332): Show |
1 | a0001c0001t0001g0189 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.478-1444_478-1443i others(341): Show |
MOSPD2 | ENSG00000130150.12 | transcript | ENST00000380492.8 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chrX | 14899114 | |||||
| chrX:14899114
|
T | TGAACTAG others(333): Show |
3 | a0001c0001t0001g0167a0001c0001t0001g0171a0001c0001t0001g0193 | 3 | HG00733.hp1 HG03017.hp1 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.478-1444_478-1443i others(342): Show |
MOSPD2 | ENSG00000130150.12 | transcript | ENST00000380492.8 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chrX | 14899114 | |||||
| chrX:14899114
|
T | TGAACTAG others(334): Show |
1 | a0001c0001t0001g0194 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.478-1444_478-1443i others(343): Show |
MOSPD2 | ENSG00000130150.12 | transcript | ENST00000380492.8 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chrX | 14899114 | |||||
| chrX:14899114
|
T | TGAACTAG others(336): Show |
1 | a0001c0001t0001g0172 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.478-1444_478-1443i others(345): Show |
MOSPD2 | ENSG00000130150.12 | transcript | ENST00000380492.8 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chrX | 14899114 | |||||
| chrX:14899114
|
T | TGAACTAG others(337): Show |
2 | a0001c0001t0001g0179a0001c0001t0001g0180 | 2 | HG01358.hp1 HG01981.hp1 |
intron_variant | MODIFIER | c.478-1444_478-1443i others(346): Show |
MOSPD2 | ENSG00000130150.12 | transcript | ENST00000380492.8 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chrX | 14899114 | |||||
| chrX:14899114
|
T | TGAACTAG others(338): Show |
3 | a0001c0001t0001g0173a0001c0001t0001g0174a0001c0001t0001g0178 | 3 | HG00609.hp1 NA18979.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.478-1444_478-1443i others(347): Show |
MOSPD2 | ENSG00000130150.12 | transcript | ENST00000380492.8 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chrX | 14899114 | |||||
| chrX:14899114
|
T | TGAACTAG others(340): Show |
1 | a0001c0001t0001g0175 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.478-1444_478-1443i others(349): Show |
MOSPD2 | ENSG00000130150.12 | transcript | ENST00000380492.8 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chrX | 14899114 | |||||
| chrX:14899114
|
T | TGAACTAG others(341): Show |
1 | a0001c0001t0001g0187 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.478-1444_478-1443i others(350): Show |
MOSPD2 | ENSG00000130150.12 | transcript | ENST00000380492.8 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chrX | 14899114 | |||||
| chrX:14899114
|
T | TGAACTAG others(343): Show |
1 | a0001c0001t0001g0192 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.478-1444_478-1443i others(352): Show |
MOSPD2 | ENSG00000130150.12 | transcript | ENST00000380492.8 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chrX | 14899114 | |||||
| chrX:14899114
|
T | TGAACTAG others(344): Show |
2 | a0001c0001t0001g0176a0001c0001t0001g0177 | 2 | NA19012.hp1 NA19091.hp1 |
intron_variant | MODIFIER | c.478-1444_478-1443i others(353): Show |
MOSPD2 | ENSG00000130150.12 | transcript | ENST00000380492.8 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chrX | 14899114 | |||||
| chrX:14899270
|
T | C | 2 | a0001c0001t0001g0061a0001c0001t0001g0062 | 2 | NA18612.hp1 NA19066.hp1 |
intron_variant | MODIFIER | c.478-1305T>C | MOSPD2 | ENSG00000130150.12 | transcript | ENST00000380492.8 | protein_coding | 5/14 | chrX | 14899270 | ||||||
| chrX:14899441
|
T | C | 4 | a0001c0001t0002g0006a0001c0001t0002g0011a0001c0001t0002g0039others(1): Show | 7 | HG01243.hp1 HG02280.hp1 HG02622.hp2 others(4): Show |
intron_variant | MODIFIER | c.478-1134T>C | MOSPD2 | ENSG00000130150.12 | transcript | ENST00000380492.8 | protein_coding | 5/14 | chrX | 14899441 | ||||||
| chrX:14899514
|
T | TTA | 3 | a0001c0001t0001g0164a0001c0001t0001g0166a0001c0004t0001g0165 | 3 | HG02630.hp1 HG02723.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.478-1048_478-1047d others(4): Show |
MOSPD2 | ENSG00000130150.12 | transcript | ENST00000380492.8 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chrX | 14899514 | |||||
| chrX:14899514
|
T | TTATA | 89 | a0001c0001t0001g0004a0001c0001t0001g0010a0001c0001t0001g0024others(86): Show | 105 | HG00140.hp1 HG00280.hp1 HG00408.hp2 others(102): Show |
intron_variant | MODIFIER | c.478-1050_478-1047d others(6): Show |
MOSPD2 | ENSG00000130150.12 | transcript | ENST00000380492.8 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chrX | 14899514 | |||||
| chrX:14899514
|
T | TTATATA | 8 | a0001c0001t0001g0051a0001c0001t0001g0127a0001c0001t0001g0128others(5): Show | 8 | HG01109.hp1 HG02109.hp1 HG02451.hp2 others(5): Show |
intron_variant | MODIFIER | c.478-1052_478-1047d others(8): Show |
MOSPD2 | ENSG00000130150.12 | transcript | ENST00000380492.8 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chrX | 14899514 | |||||
| chrX:14899527
|
T | C | 1 | a0001c0001t0007g0033 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.478-1048T>C | MOSPD2 | ENSG00000130150.12 | transcript | ENST00000380492.8 | protein_coding | 5/14 | chrX | 14899527 | ||||||
| chrX:14899565
|
T | TAC | 16 | a0001c0001t0001g0014a0001c0001t0001g0060a0001c0001t0001g0061others(13): Show | 17 | HG00408.hp1 HG00673.hp1 HG01081.hp2 others(14): Show |
intron_variant | MODIFIER | c.478-970_478-969dup others(2): Show |
MOSPD2 | ENSG00000130150.12 | transcript | ENST00000380492.8 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chrX | 14899565 | |||||
| chrX:14899565
|
T | TACAC | 25 | a0001c0001t0001g0022a0001c0001t0001g0027a0001c0001t0001g0042others(22): Show | 27 | HG00558.hp2 HG00639.hp1 HG00735.hp1 others(24): Show |
intron_variant | MODIFIER | c.478-972_478-969dup others(4): Show |
MOSPD2 | ENSG00000130150.12 | transcript | ENST00000380492.8 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chrX | 14899565 | |||||
| chrX:14899565
|
T | TACACAC | 9 | a0001c0001t0001g0121a0001c0001t0001g0142a0001c0001t0001g0172others(6): Show | 9 | HG00609.hp1 HG00733.hp1 HG00741.hp1 others(6): Show |
intron_variant | MODIFIER | c.478-974_478-969dup others(6): Show |
MOSPD2 | ENSG00000130150.12 | transcript | ENST00000380492.8 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chrX | 14899565 | |||||
| chrX:14899565
|
T | TACACACA others(1): Show |
1 | a0001c0001t0002g0203 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.478-976_478-969dup others(8): Show |
MOSPD2 | ENSG00000130150.12 | transcript | ENST00000380492.8 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chrX | 14899565 | |||||
| chrX:14899565
|
T | TACACACA others(3): Show |
6 | a0001c0001t0001g0024a0001c0001t0001g0032a0001c0001t0001g0135others(3): Show | 7 | HG00140.hp1 HG01123.hp1 HG01175.hp1 others(4): Show |
intron_variant | MODIFIER | c.478-978_478-969dup others(10): Show |
MOSPD2 | ENSG00000130150.12 | transcript | ENST00000380492.8 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chrX | 14899565 | |||||
| chrX:14899565
|
T | TACACACA others(5): Show |
4 | a0001c0001t0001g0132a0001c0001t0001g0163a0001c0003t0001g0023others(1): Show | 5 | HG01168.hp2 HG01169.hp2 HG01361.hp1 others(2): Show |
intron_variant | MODIFIER | c.478-980_478-969dup others(12): Show |
MOSPD2 | ENSG00000130150.12 | transcript | ENST00000380492.8 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chrX | 14899565 | |||||
| chrX:14899565
|
T | TACACACA others(7): Show |
2 | a0001c0001t0009g0146a0002c0002t0001g0034 | 2 | HG01256.hp1 HG02735.hp1 |
intron_variant | MODIFIER | c.478-982_478-969dup others(14): Show |
MOSPD2 | ENSG00000130150.12 | transcript | ENST00000380492.8 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chrX | 14899565 | |||||
| chrX:14899565
|
T | TACACACA others(9): Show |
2 | a0002c0002t0001g0035a0002c0002t0001g0037 | 2 | HG00280.hp1 HG01261.hp1 |
intron_variant | MODIFIER | c.478-984_478-969dup others(16): Show |
MOSPD2 | ENSG00000130150.12 | transcript | ENST00000380492.8 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chrX | 14899565 | |||||
| chrX:14899565
|
TAC | T | 46 | a0001c0001t0001g0004a0001c0001t0001g0010a0001c0001t0001g0028others(43): Show | 59 | HG00408.hp2 HG00639.hp2 HG01074.hp1 others(56): Show |
intron_variant | MODIFIER | c.478-970_478-969del others(2): Show |
MOSPD2 | ENSG00000130150.12 | transcript | ENST00000380492.8 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chrX | 14899565 | |||||
| chrX:14899565
|
TACAC | T | 11 | a0001c0001t0001g0017a0001c0001t0001g0019a0001c0001t0001g0044others(8): Show | 13 | HG00423.hp2 HG00735.hp2 HG00741.hp2 others(10): Show |
intron_variant | MODIFIER | c.478-972_478-969del others(4): Show |
MOSPD2 | ENSG00000130150.12 | transcript | ENST00000380492.8 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chrX | 14899565 | |||||
| chrX:14899565
|
TACACAC | T | 6 | a0001c0001t0001g0043a0001c0001t0001g0138a0001c0001t0002g0006others(3): Show | 8 | HG01192.hp1 HG01243.hp1 HG02280.hp1 others(5): Show |
intron_variant | MODIFIER | c.478-974_478-969del others(6): Show |
MOSPD2 | ENSG00000130150.12 | transcript | ENST00000380492.8 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chrX | 14899565 | |||||
| chrX:14899565
|
TACACACA others(1): Show |
T | 1 | a0001c0001t0002g0011 | 2 | HG02970.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.478-976_478-969del others(8): Show |
MOSPD2 | ENSG00000130150.12 | transcript | ENST00000380492.8 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chrX | 14899565 | |||||
| chrX:14899565
|
TACACACA others(3): Show |
T | 1 | a0001c0001t0007g0033 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.478-978_478-969del others(10): Show |
MOSPD2 | ENSG00000130150.12 | transcript | ENST00000380492.8 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chrX | 14899565 | |||||
| chrX:14899606
|
A | AC | 1 | a0001c0001t0001g0081 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.478-969_478-968ins others(1): Show |
MOSPD2 | ENSG00000130150.12 | transcript | ENST00000380492.8 | protein_coding | 5/14 | chrX | 14899606 | ||||||
| chrX:14899606
|
A | ACACACAC others(4): Show |
1 | a0001c0001t0001g0038 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.478-969_478-968ins others(11): Show |
MOSPD2 | ENSG00000130150.12 | transcript | ENST00000380492.8 | protein_coding | 5/14 | chrX | 14899606 | ||||||
| chrX:14899607
|
A | C | 6 | a0001c0001t0001g0168a0001c0001t0001g0169a0001c0001t0001g0170others(3): Show | 6 | NA18945.hp1 NA18950.hp1 NA18979.hp2 others(3): Show |
intron_variant | MODIFIER | c.478-968A>C | MOSPD2 | ENSG00000130150.12 | transcript | ENST00000380492.8 | protein_coding | 5/14 | chrX | 14899607 | ||||||
| chrX:14899753
|
T | C | 1 | a0001c0001t0001g0164 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.478-822T>C | MOSPD2 | ENSG00000130150.12 | transcript | ENST00000380492.8 | protein_coding | 5/14 | chrX | 14899753 | ||||||
| chrX:14900702
|
G | A | 1 | a0001c0001t0001g0147 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.538+67G>A | MOSPD2 | ENSG00000130150.12 | transcript | ENST00000380492.8 | protein_coding | 6/14 | chrX | 14900702 | ||||||
| chrX:14900715
|
A | G | 1 | a0001c0001t0002g0204 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.538+80A>G | MOSPD2 | ENSG00000130150.12 | transcript | ENST00000380492.8 | protein_coding | 6/14 | chrX | 14900715 | ||||||
| chrX:14900967
|
A | C | 1 | a0001c0001t0001g0092 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.538+332A>C | MOSPD2 | ENSG00000130150.12 | transcript | ENST00000380492.8 | protein_coding | 6/14 | chrX | 14900967 | ||||||
| chrX:14900992
|
A | G | 1 | a0001c0001t0001g0038 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.538+357A>G | MOSPD2 | ENSG00000130150.12 | transcript | ENST00000380492.8 | protein_coding | 6/14 | chrX | 14900992 | ||||||
| chrX:14901284
|
A | G | 1 | a0001c0001t0002g0204 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.538+649A>G | MOSPD2 | ENSG00000130150.12 | transcript | ENST00000380492.8 | protein_coding | 6/14 | chrX | 14901284 | ||||||
| chrX:14901329
|
T | C | 1 | a0001c0001t0005g0018 | 2 | HG01167.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.538+694T>C | MOSPD2 | ENSG00000130150.12 | transcript | ENST00000380492.8 | protein_coding | 6/14 | chrX | 14901329 | ||||||
| chrX:14901431
|
G | A | 1 | a0001c0001t0002g0203 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.538+796G>A | MOSPD2 | ENSG00000130150.12 | transcript | ENST00000380492.8 | protein_coding | 6/14 | chrX | 14901431 | ||||||
| chrX:14901635
|
G | A | 1 | a0001c0001t0001g0074 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.538+1000G>A | MOSPD2 | ENSG00000130150.12 | transcript | ENST00000380492.8 | protein_coding | 6/14 | chrX | 14901635 | ||||||
| chrX:14901741
|
A | T | 1 | a0001c0001t0001g0182 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.538+1106A>T | MOSPD2 | ENSG00000130150.12 | transcript | ENST00000380492.8 | protein_coding | 6/14 | chrX | 14901741 | ||||||
| chrX:14901966
|
T | TTA | 19 | a0001c0001t0001g0024a0001c0001t0001g0032a0001c0001t0001g0070others(16): Show | 21 | HG00140.hp1 HG00280.hp1 HG00741.hp1 others(18): Show |
intron_variant | MODIFIER | c.539-985_539-984dup others(2): Show |
MOSPD2 | ENSG00000130150.12 | transcript | ENST00000380492.8 | protein_coding | 6/14 | INFO_REALIGN_3_PRIME | chrX | 14901966 | |||||
| chrX:14901981
|
T | C | 4 | a0001c0001t0002g0006a0001c0001t0002g0011a0001c0001t0002g0039others(1): Show | 7 | HG01243.hp1 HG02280.hp1 HG02622.hp2 others(4): Show |
intron_variant | MODIFIER | c.539-985T>C | MOSPD2 | ENSG00000130150.12 | transcript | ENST00000380492.8 | protein_coding | 6/14 | chrX | 14901981 | ||||||
| chrX:14902004
|
T | C | 1 | a0001c0001t0001g0135 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.539-962T>C | MOSPD2 | ENSG00000130150.12 | transcript | ENST00000380492.8 | protein_coding | 6/14 | chrX | 14902004 | ||||||
| chrX:14902143
|
A | G | 1 | a0001c0001t0001g0058 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.539-823A>G | MOSPD2 | ENSG00000130150.12 | transcript | ENST00000380492.8 | protein_coding | 6/14 | chrX | 14902143 | ||||||
| chrX:14902307
|
A | G | 1 | a0001c0001t0002g0011 | 2 | HG02970.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.539-659A>G | MOSPD2 | ENSG00000130150.12 | transcript | ENST00000380492.8 | protein_coding | 6/14 | chrX | 14902307 | ||||||
| chrX:14902463
|
T | C | 1 | a0001c0001t0001g0038 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.539-503T>C | MOSPD2 | ENSG00000130150.12 | transcript | ENST00000380492.8 | protein_coding | 6/14 | chrX | 14902463 | ||||||
| chrX:14902494
|
G | A | 2 | a0001c0001t0001g0080a0001c0001t0001g0096 | 2 | HG02027.hp1 NA19063.hp1 |
intron_variant | MODIFIER | c.539-472G>A | MOSPD2 | ENSG00000130150.12 | transcript | ENST00000380492.8 | protein_coding | 6/14 | chrX | 14902494 | ||||||
| chrX:14902512
|
G | C | 1 | a0001c0001t0001g0116 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.539-454G>C | MOSPD2 | ENSG00000130150.12 | transcript | ENST00000380492.8 | protein_coding | 6/14 | chrX | 14902512 | ||||||
| chrX:14902600
|
C | T | 1 | a0001c0001t0008g0162 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.539-366C>T | MOSPD2 | ENSG00000130150.12 | transcript | ENST00000380492.8 | protein_coding | 6/14 | chrX | 14902600 | ||||||
| chrX:14902617
|
C | G | 26 | a0001c0001t0001g0027a0001c0001t0001g0167a0001c0001t0001g0168others(23): Show | 27 | HG00558.hp2 HG00609.hp1 HG00639.hp1 others(24): Show |
intron_variant | MODIFIER | c.539-349C>G | MOSPD2 | ENSG00000130150.12 | transcript | ENST00000380492.8 | protein_coding | 6/14 | chrX | 14902617 | ||||||
| chrX:14902621
|
A | G | 114 | a0001c0001t0001g0004a0001c0001t0001g0010a0001c0001t0001g0024others(111): Show | 138 | HG00140.hp1 HG00280.hp1 HG00408.hp2 others(135): Show |
intron_variant | MODIFIER | c.539-345A>G | MOSPD2 | ENSG00000130150.12 | transcript | ENST00000380492.8 | protein_coding | 6/14 | chrX | 14902621 | ||||||
| chrX:14902732
|
G | A | 1 | a0001c0001t0007g0033 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.539-234G>A | MOSPD2 | ENSG00000130150.12 | transcript | ENST00000380492.8 | protein_coding | 6/14 | chrX | 14902732 | ||||||
| chrX:14902925
|
G | A | 1 | a0001c0001t0001g0145 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.539-41G>A | MOSPD2 | ENSG00000130150.12 | transcript | ENST00000380492.8 | protein_coding | 6/14 | chrX | 14902925 | ||||||
| chrX:14903183
|
C | T | 1 | a0001c0001t0001g0154 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.577+179C>T | MOSPD2 | ENSG00000130150.12 | transcript | ENST00000380492.8 | protein_coding | 7/14 | chrX | 14903183 | ||||||
| chrX:14903288
|
C | T | 3 | a0001c0001t0001g0169a0001c0001t0001g0173a0001c0001t0001g0174 | 3 | NA18950.hp1 NA18979.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.577+284C>T | MOSPD2 | ENSG00000130150.12 | transcript | ENST00000380492.8 | protein_coding | 7/14 | chrX | 14903288 | ||||||
| chrX:14903295
|
A | G | 114 | a0001c0001t0001g0004a0001c0001t0001g0010a0001c0001t0001g0024others(111): Show | 138 | HG00140.hp1 HG00280.hp1 HG00408.hp2 others(135): Show |
intron_variant | MODIFIER | c.577+291A>G | MOSPD2 | ENSG00000130150.12 | transcript | ENST00000380492.8 | protein_coding | 7/14 | chrX | 14903295 | ||||||
| chrX:14903343
|
T | TA | 96 | a0001c0001t0001g0004a0001c0001t0001g0008a0001c0001t0001g0010others(93): Show | 115 | HG00140.hp1 HG00280.hp1 HG00408.hp2 others(112): Show |
intron_variant | MODIFIER | c.577+354dupA | MOSPD2 | ENSG00000130150.12 | transcript | ENST00000380492.8 | protein_coding | 7/14 | INFO_REALIGN_3_PRIME | chrX | 14903343 | |||||
| chrX:14903343
|
TA | T | 1 | a0001c0001t0001g0038 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.577+354delA | MOSPD2 | ENSG00000130150.12 | transcript | ENST00000380492.8 | protein_coding | 7/14 | INFO_REALIGN_3_PRIME | chrX | 14903343 | |||||
| chrX:14903343
|
TAAAAAA | T | 1 | a0001c0001t0001g0084 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.577+349_577+354del others(6): Show |
MOSPD2 | ENSG00000130150.12 | transcript | ENST00000380492.8 | protein_coding | 7/14 | INFO_REALIGN_3_PRIME | chrX | 14903343 | |||||
| chrX:14903655
|
A | C | 2 | a0001c0001t0001g0077a0001c0001t0001g0152 | 2 | HG00408.hp2 HG02132.hp1 |
intron_variant | MODIFIER | c.577+651A>C | MOSPD2 | ENSG00000130150.12 | transcript | ENST00000380492.8 | protein_coding | 7/14 | chrX | 14903655 | ||||||
| chrX:14903660
|
C | G | 3 | a0001c0001t0004g0200a0001c0001t0004g0201a0001c0001t0004g0202 | 3 | HG02809.hp1 HG02922.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.577+656C>G | MOSPD2 | ENSG00000130150.12 | transcript | ENST00000380492.8 | protein_coding | 7/14 | chrX | 14903660 | ||||||
| chrX:14904007
|
C | CA | 1 | a0001c0001t0001g0096 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.577+1011dupA | MOSPD2 | ENSG00000130150.12 | transcript | ENST00000380492.8 | protein_coding | 7/14 | INFO_REALIGN_3_PRIME | chrX | 14904007 | |||||
| chrX:14904591
|
G | C | 3 | a0001c0001t0001g0195a0001c0001t0001g0196a0001c0001t0001g0197 | 3 | HG03041.hp1 HG06807.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.577+1587G>C | MOSPD2 | ENSG00000130150.12 | transcript | ENST00000380492.8 | protein_coding | 7/14 | chrX | 14904591 | ||||||
| chrX:14905318
|
ATGT | A | 2 | a0001c0003t0001g0023a0001c0003t0001g0137 | 3 | HG01168.hp2 HG01169.hp2 HG01175.hp1 |
intron_variant | MODIFIER | c.577+2319_577+2321d others(5): Show |
MOSPD2 | ENSG00000130150.12 | transcript | ENST00000380492.8 | protein_coding | 7/14 | INFO_REALIGN_3_PRIME | chrX | 14905318 | |||||
| chrX:14905334
|
G | T | 9 | a0001c0001t0002g0003a0001c0001t0002g0006a0001c0001t0002g0011others(6): Show | 17 | HG01106.hp1 HG01243.hp1 HG01891.hp1 others(14): Show |
intron_variant | MODIFIER | c.577+2330G>T | MOSPD2 | ENSG00000130150.12 | transcript | ENST00000380492.8 | protein_coding | 7/14 | chrX | 14905334 | ||||||
| chrX:14905492
|
C | CT | 1 | a0001c0001t0001g0038 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.577+2497dupT | MOSPD2 | ENSG00000130150.12 | transcript | ENST00000380492.8 | protein_coding | 7/14 | INFO_REALIGN_3_PRIME | chrX | 14905492 | |||||
| chrX:14905616
|
C | T | 1 | a0001c0001t0001g0062 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.577+2612C>T | MOSPD2 | ENSG00000130150.12 | transcript | ENST00000380492.8 | protein_coding | 7/14 | chrX | 14905616 | ||||||
| chrX:14906155
|
G | A | 1 | a0001c0001t0001g0173 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.578-2705G>A | MOSPD2 | ENSG00000130150.12 | transcript | ENST00000380492.8 | protein_coding | 7/14 | chrX | 14906155 | ||||||
| chrX:14906318
|
A | G | 1 | a0002c0002t0001g0037 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.578-2542A>G | MOSPD2 | ENSG00000130150.12 | transcript | ENST00000380492.8 | protein_coding | 7/14 | chrX | 14906318 | ||||||
| chrX:14906565
|
T | TAAAC | 114 | a0001c0001t0001g0004a0001c0001t0001g0010a0001c0001t0001g0024others(111): Show | 138 | HG00140.hp1 HG00280.hp1 HG00408.hp2 others(135): Show |
intron_variant | MODIFIER | c.578-2293_578-2290d others(6): Show |
MOSPD2 | ENSG00000130150.12 | transcript | ENST00000380492.8 | protein_coding | 7/14 | INFO_REALIGN_3_PRIME | chrX | 14906565 | |||||
| chrX:14906624
|
A | G | 1 | a0001c0001t0001g0154 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.578-2236A>G | MOSPD2 | ENSG00000130150.12 | transcript | ENST00000380492.8 | protein_coding | 7/14 | chrX | 14906624 | ||||||
| chrX:14906763
|
G | A | 1 | a0001c0001t0001g0052 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.578-2097G>A | MOSPD2 | ENSG00000130150.12 | transcript | ENST00000380492.8 | protein_coding | 7/14 | chrX | 14906763 | ||||||
| chrX:14906939
|
G | A | 99 | a0001c0001t0001g0004a0001c0001t0001g0010a0001c0001t0001g0024others(96): Show | 115 | HG00140.hp1 HG00280.hp1 HG00408.hp2 others(112): Show |
intron_variant | MODIFIER | c.578-1921G>A | MOSPD2 | ENSG00000130150.12 | transcript | ENST00000380492.8 | protein_coding | 7/14 | chrX | 14906939 | ||||||
| chrX:14906963
|
G | T | 3 | a0001c0001t0002g0006a0001c0001t0002g0039a0001c0001t0002g0040 | 5 | HG01243.hp1 HG02280.hp1 HG02622.hp2 others(2): Show |
intron_variant | MODIFIER | c.578-1897G>T | MOSPD2 | ENSG00000130150.12 | transcript | ENST00000380492.8 | protein_coding | 7/14 | chrX | 14906963 | ||||||
| chrX:14906980
|
C | T | 1 | a0001c0001t0008g0162 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.578-1880C>T | MOSPD2 | ENSG00000130150.12 | transcript | ENST00000380492.8 | protein_coding | 7/14 | chrX | 14906980 | ||||||
| chrX:14907087
|
G | T | 1 | a0001c0001t0008g0162 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.578-1773G>T | MOSPD2 | ENSG00000130150.12 | transcript | ENST00000380492.8 | protein_coding | 7/14 | chrX | 14907087 | ||||||
| chrX:14907283
|
G | T | 1 | a0001c0001t0001g0076 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.578-1577G>T | MOSPD2 | ENSG00000130150.12 | transcript | ENST00000380492.8 | protein_coding | 7/14 | chrX | 14907283 | ||||||
| chrX:14907380
|
G | A | 114 | a0001c0001t0001g0004a0001c0001t0001g0010a0001c0001t0001g0024others(111): Show | 138 | HG00140.hp1 HG00280.hp1 HG00408.hp2 others(135): Show |
intron_variant | MODIFIER | c.578-1480G>A | MOSPD2 | ENSG00000130150.12 | transcript | ENST00000380492.8 | protein_coding | 7/14 | chrX | 14907380 | ||||||
| chrX:14907780
|
A | G | 11 | a0001c0001t0001g0038a0001c0001t0002g0003a0001c0001t0002g0006others(8): Show | 19 | HG01106.hp1 HG01243.hp1 HG01891.hp1 others(16): Show |
intron_variant | MODIFIER | c.578-1080A>G | MOSPD2 | ENSG00000130150.12 | transcript | ENST00000380492.8 | protein_coding | 7/14 | chrX | 14907780 | ||||||
| chrX:14907964
|
T | A | 1 | a0001c0001t0007g0033 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.578-896T>A | MOSPD2 | ENSG00000130150.12 | transcript | ENST00000380492.8 | protein_coding | 7/14 | chrX | 14907964 | ||||||
| chrX:14908566
|
G | T | 1 | a0001c0001t0001g0182 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.578-294G>T | MOSPD2 | ENSG00000130150.12 | transcript | ENST00000380492.8 | protein_coding | 7/14 | chrX | 14908566 | ||||||
| chrX:14909142
|
TTTAAAG | T | 3 | a0001c0001t0002g0006a0001c0001t0002g0039a0001c0001t0002g0040 | 5 | HG01243.hp1 HG02280.hp1 HG02622.hp2 others(2): Show |
intron_variant | MODIFIER | c.702+163_702+168del others(6): Show |
MOSPD2 | ENSG00000130150.12 | transcript | ENST00000380492.8 | protein_coding | 8/14 | INFO_REALIGN_3_PRIME | chrX | 14909142 | |||||
| chrX:14909285
|
A | G | 1 | a0001c0001t0001g0157 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.702+301A>G | MOSPD2 | ENSG00000130150.12 | transcript | ENST00000380492.8 | protein_coding | 8/14 | chrX | 14909285 | ||||||
| chrX:14909379
|
C | T | 1 | a0001c0001t0011g0136 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.702+395C>T | MOSPD2 | ENSG00000130150.12 | transcript | ENST00000380492.8 | protein_coding | 8/14 | chrX | 14909379 | ||||||
| chrX:14909457
|
C | T | 1 | a0001c0001t0001g0120 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.702+473C>T | MOSPD2 | ENSG00000130150.12 | transcript | ENST00000380492.8 | protein_coding | 8/14 | chrX | 14909457 | ||||||
| chrX:14909601
|
C | A | 1 | a0001c0001t0008g0162 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.702+617C>A | MOSPD2 | ENSG00000130150.12 | transcript | ENST00000380492.8 | protein_coding | 8/14 | chrX | 14909601 | ||||||
| chrX:14909780
|
T | C | 4 | a0001c0001t0001g0130a0001c0001t0001g0151a0001c0001t0001g0158others(1): Show | 4 | HG00423.hp2 NA18946.hp2 NA18962.hp1 others(1): Show |
intron_variant | MODIFIER | c.702+796T>C | MOSPD2 | ENSG00000130150.12 | transcript | ENST00000380492.8 | protein_coding | 8/14 | chrX | 14909780 | ||||||
| chrX:14910035
|
T | C | 3 | a0001c0001t0001g0015a0001c0001t0001g0100a0001c0001t0001g0103 | 4 | HG02071.hp1 HG02083.hp1 HG02148.hp2 others(1): Show |
intron_variant | MODIFIER | c.702+1051T>C | MOSPD2 | ENSG00000130150.12 | transcript | ENST00000380492.8 | protein_coding | 8/14 | chrX | 14910035 | ||||||
| chrX:14910108
|
ATAG | A | 1 | a0001c0004t0001g0165 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.703-1125_703-1123d others(5): Show |
MOSPD2 | ENSG00000130150.12 | transcript | ENST00000380492.8 | protein_coding | 8/14 | INFO_REALIGN_3_PRIME | chrX | 14910108 | |||||
| chrX:14910146
|
AT | A | 3 | a0001c0001t0002g0006a0001c0001t0002g0039a0001c0001t0002g0040 | 5 | HG01243.hp1 HG02280.hp1 HG02622.hp2 others(2): Show |
intron_variant | MODIFIER | c.703-1083delT | MOSPD2 | ENSG00000130150.12 | transcript | ENST00000380492.8 | protein_coding | 8/14 | INFO_REALIGN_3_PRIME | chrX | 14910146 | |||||
| chrX:14910155
|
C | A | 25 | a0001c0001t0001g0004a0001c0001t0001g0010a0001c0001t0001g0047others(22): Show | 30 | HG00408.hp2 HG00423.hp2 HG01070.hp1 others(27): Show |
intron_variant | MODIFIER | c.703-1082C>A | MOSPD2 | ENSG00000130150.12 | transcript | ENST00000380492.8 | protein_coding | 8/14 | chrX | 14910155 | ||||||
| chrX:14910592
|
C | T | 1 | a0001c0001t0001g0123 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.703-645C>T | MOSPD2 | ENSG00000130150.12 | transcript | ENST00000380492.8 | protein_coding | 8/14 | chrX | 14910592 | ||||||
| chrX:14910622
|
A | C | 2 | a0001c0001t0001g0050a0001c0001t0001g0085 | 2 | NA18969.hp1 NA19006.hp1 |
intron_variant | MODIFIER | c.703-615A>C | MOSPD2 | ENSG00000130150.12 | transcript | ENST00000380492.8 | protein_coding | 8/14 | chrX | 14910622 | ||||||
| chrX:14910672
|
T | C | 1 | a0001c0001t0001g0194 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.703-565T>C | MOSPD2 | ENSG00000130150.12 | transcript | ENST00000380492.8 | protein_coding | 8/14 | chrX | 14910672 | ||||||
| chrX:14910841
|
T | A | 1 | a0001c0001t0001g0101 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.703-396T>A | MOSPD2 | ENSG00000130150.12 | transcript | ENST00000380492.8 | protein_coding | 8/14 | chrX | 14910841 | ||||||
| chrX:14910931
|
T | TAC | 72 | a0001c0001t0001g0004a0001c0001t0001g0010a0001c0001t0001g0022others(69): Show | 88 | HG00140.hp1 HG00280.hp1 HG00408.hp2 others(85): Show |
intron_variant | MODIFIER | c.703-278_703-277dup others(2): Show |
MOSPD2 | ENSG00000130150.12 | transcript | ENST00000380492.8 | protein_coding | 8/14 | INFO_REALIGN_3_PRIME | chrX | 14910931 | |||||
| chrX:14910931
|
T | TACAC | 7 | a0001c0001t0001g0044a0001c0001t0001g0129a0001c0001t0001g0133others(4): Show | 7 | HG02109.hp1 HG02615.hp1 HG02809.hp1 others(4): Show |
intron_variant | MODIFIER | c.703-280_703-277dup others(4): Show |
MOSPD2 | ENSG00000130150.12 | transcript | ENST00000380492.8 | protein_coding | 8/14 | INFO_REALIGN_3_PRIME | chrX | 14910931 | |||||
| chrX:14910931
|
T | TACACAC | 24 | a0001c0001t0001g0027a0001c0001t0001g0167a0001c0001t0001g0168others(21): Show | 25 | HG00558.hp2 HG00609.hp1 HG00639.hp1 others(22): Show |
intron_variant | MODIFIER | c.703-282_703-277dup others(6): Show |
MOSPD2 | ENSG00000130150.12 | transcript | ENST00000380492.8 | protein_coding | 8/14 | INFO_REALIGN_3_PRIME | chrX | 14910931 | |||||
| chrX:14910931
|
T | TACACACA others(1): Show |
1 | a0001c0001t0001g0194 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.703-284_703-277dup others(8): Show |
MOSPD2 | ENSG00000130150.12 | transcript | ENST00000380492.8 | protein_coding | 8/14 | INFO_REALIGN_3_PRIME | chrX | 14910931 | |||||
| chrX:14910931
|
TAC | T | 6 | a0001c0001t0001g0038a0001c0001t0001g0164a0001c0001t0001g0166others(3): Show | 6 | HG02630.hp1 HG02723.hp1 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.703-278_703-277del others(2): Show |
MOSPD2 | ENSG00000130150.12 | transcript | ENST00000380492.8 | protein_coding | 8/14 | INFO_REALIGN_3_PRIME | chrX | 14910931 | |||||
| chrX:14910931
|
TACAC | T | 9 | a0001c0001t0002g0003a0001c0001t0002g0006a0001c0001t0002g0011others(6): Show | 17 | HG01106.hp1 HG01243.hp1 HG01891.hp1 others(14): Show |
intron_variant | MODIFIER | c.703-280_703-277del others(4): Show |
MOSPD2 | ENSG00000130150.12 | transcript | ENST00000380492.8 | protein_coding | 8/14 | INFO_REALIGN_3_PRIME | chrX | 14910931 | |||||
| chrX:14910981
|
C | T | 1 | a0001c0004t0001g0165 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.703-256C>T | MOSPD2 | ENSG00000130150.12 | transcript | ENST00000380492.8 | protein_coding | 8/14 | chrX | 14910981 | ||||||
| chrX:14911201
|
C | A | 2 | a0001c0001t0001g0050a0001c0001t0001g0085 | 2 | NA18969.hp1 NA19006.hp1 |
intron_variant | MODIFIER | c.703-36C>A | MOSPD2 | ENSG00000130150.12 | transcript | ENST00000380492.8 | protein_coding | 8/14 | chrX | 14911201 | ||||||
| chrX:14911667
|
C | T | 1 | a0001c0001t0001g0167 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.879+254C>T | MOSPD2 | ENSG00000130150.12 | transcript | ENST00000380492.8 | protein_coding | 9/14 | chrX | 14911667 | ||||||
| chrX:14911753
|
G | A | 11 | a0001c0001t0001g0038a0001c0001t0002g0003a0001c0001t0002g0006others(8): Show | 19 | HG01106.hp1 HG01243.hp1 HG01891.hp1 others(16): Show |
intron_variant | MODIFIER | c.879+340G>A | MOSPD2 | ENSG00000130150.12 | transcript | ENST00000380492.8 | protein_coding | 9/14 | chrX | 14911753 | ||||||
| chrX:14911820
|
G | A | 4 | a0001c0001t0001g0127a0001c0001t0001g0128a0001c0001t0001g0129others(1): Show | 4 | HG01109.hp1 HG02109.hp1 HG02976.hp1 others(1): Show |
intron_variant | MODIFIER | c.879+407G>A | MOSPD2 | ENSG00000130150.12 | transcript | ENST00000380492.8 | protein_coding | 9/14 | chrX | 14911820 | ||||||
| chrX:14912070
|
G | T | 4 | a0001c0001t0001g0017a0001c0001t0001g0019a0001c0001t0001g0107others(1): Show | 6 | HG00735.hp2 HG00741.hp2 HG01123.hp2 others(3): Show |
intron_variant | MODIFIER | c.880-179G>T | MOSPD2 | ENSG00000130150.12 | transcript | ENST00000380492.8 | protein_coding | 9/14 | chrX | 14912070 | ||||||
| chrX:14912090
|
T | A | 1 | a0001c0001t0001g0049 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.880-159T>A | MOSPD2 | ENSG00000130150.12 | transcript | ENST00000380492.8 | protein_coding | 9/14 | chrX | 14912090 | ||||||
| chrX:14912231
|
C | CT | 115 | a0001c0001t0001g0004a0001c0001t0001g0010a0001c0001t0001g0024others(112): Show | 139 | HG00140.hp1 HG00280.hp1 HG00408.hp2 others(136): Show |
splice_region_variant&intron_variant | LOW | c.880-9dupT | MOSPD2 | ENSG00000130150.12 | transcript | ENST00000380492.8 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chrX | 14912231 | |||||
| chrX:14912432
|
T | A | 1 | a0001c0001t0001g0082 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.992+71T>A | MOSPD2 | ENSG00000130150.12 | transcript | ENST00000380492.8 | protein_coding | 10/14 | chrX | 14912432 | ||||||
| chrX:14912551
|
T | C | 1 | a0001c0001t0001g0164 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.992+190T>C | MOSPD2 | ENSG00000130150.12 | transcript | ENST00000380492.8 | protein_coding | 10/14 | chrX | 14912551 | ||||||
| chrX:14912653
|
T | C | 1 | a0001c0001t0001g0128 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.992+292T>C | MOSPD2 | ENSG00000130150.12 | transcript | ENST00000380492.8 | protein_coding | 10/14 | chrX | 14912653 | ||||||
| chrX:14912902
|
G | A | 1 | a0002c0002t0001g0037 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.992+541G>A | MOSPD2 | ENSG00000130150.12 | transcript | ENST00000380492.8 | protein_coding | 10/14 | chrX | 14912902 | ||||||
| chrX:14913104
|
C | T | 2 | a0001c0001t0001g0072a0001c0001t0001g0079 | 2 | NA18986.hp1 NA19004.hp1 |
intron_variant | MODIFIER | c.992+743C>T | MOSPD2 | ENSG00000130150.12 | transcript | ENST00000380492.8 | protein_coding | 10/14 | chrX | 14913104 | ||||||
| chrX:14913583
|
A | G | 1 | a0002c0002t0001g0037 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.993-920A>G | MOSPD2 | ENSG00000130150.12 | transcript | ENST00000380492.8 | protein_coding | 10/14 | chrX | 14913583 | ||||||
| chrX:14913587
|
C | G | 10 | a0001c0001t0001g0156a0001c0001t0002g0003a0001c0001t0002g0006others(7): Show | 18 | HG01106.hp1 HG01243.hp1 HG01891.hp1 others(15): Show |
intron_variant | MODIFIER | c.993-916C>G | MOSPD2 | ENSG00000130150.12 | transcript | ENST00000380492.8 | protein_coding | 10/14 | chrX | 14913587 | ||||||
| chrX:14914249
|
ACT | A | 9 | a0001c0001t0003g0005a0001c0001t0003g0007a0001c0001t0003g0026others(6): Show | 15 | HG01074.hp1 HG01884.hp1 HG01891.hp2 others(12): Show |
intron_variant | MODIFIER | c.993-247_993-246del others(2): Show |
MOSPD2 | ENSG00000130150.12 | transcript | ENST00000380492.8 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chrX | 14914249 | |||||
| chrX:14914371
|
A | T | 1 | a0001c0001t0001g0071 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.993-132A>T | MOSPD2 | ENSG00000130150.12 | transcript | ENST00000380492.8 | protein_coding | 10/14 | chrX | 14914371 | ||||||
| chrX:14914498
|
C | A | 3 | a0001c0001t0001g0164a0001c0001t0001g0166a0001c0004t0001g0165 | 3 | HG02630.hp1 HG02723.hp1 HG02886.hp1 |
splice_region_variant&intron_variant | LOW | c.993-5C>A | MOSPD2 | ENSG00000130150.12 | transcript | ENST00000380492.8 | protein_coding | 10/14 | chrX | 14914498 | ||||||
| chrX:14914650
|
A | G | 3 | a0001c0001t0001g0164a0001c0001t0001g0166a0001c0004t0001g0165 | 3 | HG02630.hp1 HG02723.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.1089+51A>G | MOSPD2 | ENSG00000130150.12 | transcript | ENST00000380492.8 | protein_coding | 11/14 | chrX | 14914650 | ||||||
| chrX:14914762
|
G | T | 5 | a0001c0001t0002g0003a0001c0001t0002g0012a0001c0001t0002g0031others(2): Show | 10 | HG01106.hp1 HG01891.hp1 HG02109.hp2 others(7): Show |
intron_variant | MODIFIER | c.1089+163G>T | MOSPD2 | ENSG00000130150.12 | transcript | ENST00000380492.8 | protein_coding | 11/14 | chrX | 14914762 | ||||||
| chrX:14914985
|
G | A | 2 | a0001c0001t0001g0020a0001c0001t0001g0021 | 4 | HG01070.hp2 HG01071.hp1 HG02257.hp1 others(1): Show |
intron_variant | MODIFIER | c.1089+386G>A | MOSPD2 | ENSG00000130150.12 | transcript | ENST00000380492.8 | protein_coding | 11/14 | chrX | 14914985 | ||||||
| chrX:14915483
|
C | T | 3 | a0001c0001t0002g0003a0001c0001t0002g0012a0001c0001t0002g0031 | 8 | HG01106.hp1 HG01891.hp1 HG02109.hp2 others(5): Show |
intron_variant | MODIFIER | c.1090-185C>T | MOSPD2 | ENSG00000130150.12 | transcript | ENST00000380492.8 | protein_coding | 11/14 | chrX | 14915483 | ||||||
| chrX:14915539
|
A | G | 17 | a0001c0001t0001g0025a0001c0001t0001g0051a0001c0001t0001g0127others(14): Show | 24 | HG00733.hp2 HG01069.hp1 HG01071.hp2 others(21): Show |
intron_variant | MODIFIER | c.1090-129A>G | MOSPD2 | ENSG00000130150.12 | transcript | ENST00000380492.8 | protein_coding | 11/14 | chrX | 14915539 | ||||||
| chrX:14916654
|
A | ATCTAAAT others(2): Show |
5 | a0001c0001t0002g0003a0001c0001t0002g0012a0001c0001t0002g0031others(2): Show | 10 | HG01106.hp1 HG01891.hp1 HG02109.hp2 others(7): Show |
intron_variant | MODIFIER | c.1316+330_1316+338d others(11): Show |
MOSPD2 | ENSG00000130150.12 | transcript | ENST00000380492.8 | protein_coding | 13/14 | INFO_REALIGN_3_PRIME | chrX | 14916654 | |||||
| chrX:14916870
|
T | C | 1 | a0001c0001t0001g0124 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.1316+544T>C | MOSPD2 | ENSG00000130150.12 | transcript | ENST00000380492.8 | protein_coding | 13/14 | chrX | 14916870 | ||||||
| chrX:14916914
|
TGAAAA | T | 1 | a0001c0001t0001g0194 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.1316+591_1316+595d others(7): Show |
MOSPD2 | ENSG00000130150.12 | transcript | ENST00000380492.8 | protein_coding | 13/14 | INFO_REALIGN_3_PRIME | chrX | 14916914 | |||||
| chrX:14917229
|
G | A | 112 | a0001c0001t0001g0004a0001c0001t0001g0010a0001c0001t0001g0024others(109): Show | 136 | HG00140.hp1 HG00280.hp1 HG00408.hp2 others(133): Show |
intron_variant | MODIFIER | c.1316+903G>A | MOSPD2 | ENSG00000130150.12 | transcript | ENST00000380492.8 | protein_coding | 13/14 | chrX | 14917229 | ||||||
| chrX:14917269
|
G | A | 1 | a0001c0001t0001g0121 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.1316+943G>A | MOSPD2 | ENSG00000130150.12 | transcript | ENST00000380492.8 | protein_coding | 13/14 | chrX | 14917269 | ||||||
| chrX:14917376
|
C | T | 1 | a0001c0001t0007g0033 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.1316+1050C>T | MOSPD2 | ENSG00000130150.12 | transcript | ENST00000380492.8 | protein_coding | 13/14 | chrX | 14917376 | ||||||
| chrX:14917379
|
T | C | 1 | a0001c0001t0001g0143 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.1316+1053T>C | MOSPD2 | ENSG00000130150.12 | transcript | ENST00000380492.8 | protein_coding | 13/14 | chrX | 14917379 | ||||||
| chrX:14917471
|
T | G | 1 | a0001c0001t0008g0162 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.1316+1145T>G | MOSPD2 | ENSG00000130150.12 | transcript | ENST00000380492.8 | protein_coding | 13/14 | chrX | 14917471 | ||||||
| chrX:14917826
|
C | G | 1 | a0001c0001t0007g0033 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.1317-854C>G | MOSPD2 | ENSG00000130150.12 | transcript | ENST00000380492.8 | protein_coding | 13/14 | chrX | 14917826 | ||||||
| chrX:14917983
|
G | GA | 1 | a0001c0001t0002g0039 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.1317-696dupA | MOSPD2 | ENSG00000130150.12 | transcript | ENST00000380492.8 | protein_coding | 13/14 | INFO_REALIGN_3_PRIME | chrX | 14917983 | |||||
| chrX:14918048
|
A | T | 5 | a0001c0001t0002g0003a0001c0001t0002g0012a0001c0001t0002g0031others(2): Show | 10 | HG01106.hp1 HG01891.hp1 HG02109.hp2 others(7): Show |
intron_variant | MODIFIER | c.1317-632A>T | MOSPD2 | ENSG00000130150.12 | transcript | ENST00000380492.8 | protein_coding | 13/14 | chrX | 14918048 | ||||||
| chrX:14918069
|
T | C | 1 | a0001c0001t0001g0105 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.1317-611T>C | MOSPD2 | ENSG00000130150.12 | transcript | ENST00000380492.8 | protein_coding | 13/14 | chrX | 14918069 | ||||||
| chrX:14918107
|
G | A | 3 | a0001c0001t0001g0164a0001c0001t0001g0166a0001c0004t0001g0165 | 3 | HG02630.hp1 HG02723.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.1317-573G>A | MOSPD2 | ENSG00000130150.12 | transcript | ENST00000380492.8 | protein_coding | 13/14 | chrX | 14918107 | ||||||
| chrX:14918269
|
C | T | 1 | a0001c0001t0002g0040 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.1317-411C>T | MOSPD2 | ENSG00000130150.12 | transcript | ENST00000380492.8 | protein_coding | 13/14 | chrX | 14918269 | ||||||
| chrX:14918276
|
A | G | 3 | a0001c0001t0001g0164a0001c0001t0001g0166a0001c0004t0001g0165 | 3 | HG02630.hp1 HG02723.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.1317-404A>G | MOSPD2 | ENSG00000130150.12 | transcript | ENST00000380492.8 | protein_coding | 13/14 | chrX | 14918276 | ||||||
| chrX:14918823
|
C | T | 2 | a0001c0001t0001g0014a0001c0001t0006g0014 | 2 | HG01081.hp2 HG01099.hp1 |
intron_variant | MODIFIER | c.1419+41C>T | MOSPD2 | ENSG00000130150.12 | transcript | ENST00000380492.8 | protein_coding | 14/14 | chrX | 14918823 | ||||||
| chrX:14918895
|
T | C | 1 | a0001c0001t0001g0132 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.1419+113T>C | MOSPD2 | ENSG00000130150.12 | transcript | ENST00000380492.8 | protein_coding | 14/14 | chrX | 14918895 | ||||||
| chrX:14919186
|
ACAGAAC | A | 1 | a0001c0001t0007g0033 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.1419+405_1419+410d others(8): Show |
MOSPD2 | ENSG00000130150.12 | transcript | ENST00000380492.8 | protein_coding | 14/14 | chrX | 14919186 | ||||||
| chrX:14919303
|
C | T | 1 | a0001c0001t0007g0033 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.1420-369C>T | MOSPD2 | ENSG00000130150.12 | transcript | ENST00000380492.8 | protein_coding | 14/14 | chrX | 14919303 | ||||||
| chrX:14919428
|
A | G | 1 | a0001c0001t0001g0174 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.1420-244A>G | MOSPD2 | ENSG00000130150.12 | transcript | ENST00000380492.8 | protein_coding | 14/14 | chrX | 14919428 |