Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| geneid | 6845 |
|---|---|
| ensemblid | ENSG00000124333.16 |
| hgncid | 11486 |
| symbol | VAMP7 |
| name | vesicle associated membrane protein 7 |
| refseq_nuc | NM_005638.6 |
| refseq_prot | NP_005629.1 |
| ensembl_nuc | ENST00000286448.12 |
| ensembl_prot | ENSP00000286448.6 |
| mane_status | MANE Select |
| chr | chrX |
| start | 155881345 |
| end | 155943769 |
| strand | + |
| ver | v1.2 |
| region | chrX:155881345-155943769 |
| region5000 | chrX:155876345-155948769 |
| regionname0 | VAMP7_chrX_155881345_155943769 |
| regionname5000 | VAMP7_chrX_155876345_155948769 |
| ahapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 220 | 184 | 59 | 34 | 73 | 6 | 10 | 56 | VAMP7_chrX_155876345_155948769 | VAMP7 | copy fasta | chrX | 155876345 | 155948769 |
| chapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| c0001 | 1/1 | 663 | 181 | 56 | 34 | 73 | 6 | 10 | VAMP7_chrX_155876345_155948769 | VAMP7 | copy fasta | chrX | 155876345 | 155948769 |
| c0002 | 0/0 | 663 | 3 | 3 | 0 | 0 | 0 | 0 | VAMP7_chrX_155876345_155948769 | VAMP7 | copy fasta | chrX | 155876345 | 155948769 |
| thapid | grch38chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| t0001 | 1/1 | 1932 | 162 | 55 | 24 | 69 | 3 | 9 | VAMP7_chrX_155876345_155948769 | VAMP7 | copy fasta | chrX | 155876345 | 155948769 |
| t0002 | 0/0 | 1932 | 17 | 1 | 10 | 2 | 3 | 1 | VAMP7_chrX_155876345_155948769 | VAMP7 | copy fasta | chrX | 155876345 | 155948769 |
| t0003 | 0/0 | 1932 | 1 | 1 | 0 | 0 | 0 | 0 | VAMP7_chrX_155876345_155948769 | VAMP7 | copy fasta | chrX | 155876345 | 155948769 |
| t0004 | 0/0 | 1932 | 1 | 1 | 0 | 0 | 0 | 0 | VAMP7_chrX_155876345_155948769 | VAMP7 | copy fasta | chrX | 155876345 | 155948769 |
| t0005 | 0/0 | 1932 | 1 | 0 | 0 | 1 | 0 | 0 | VAMP7_chrX_155876345_155948769 | VAMP7 | copy fasta | chrX | 155876345 | 155948769 |
| t0006 | 0/0 | 1932 | 1 | 1 | 0 | 0 | 0 | 0 | VAMP7_chrX_155876345_155948769 | VAMP7 | copy fasta | chrX | 155876345 | 155948769 |
| t0007 | 0/0 | 1932 | 1 | 0 | 0 | 1 | 0 | 0 | VAMP7_chrX_155876345_155948769 | VAMP7 | copy fasta | chrX | 155876345 | 155948769 |
| ghapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| g0001 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | VAMP7_chrX_155876345_155948769 | VAMP7 | chrX | 155876345 | 155948769 |
| g0002 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | VAMP7_chrX_155876345_155948769 | VAMP7 | chrX | 155876345 | 155948769 |
| g0003 | 0/0 | 3 | 1 | 1 | 0 | 1 | 0 | VAMP7_chrX_155876345_155948769 | VAMP7 | chrX | 155876345 | 155948769 |
| g0004 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | VAMP7_chrX_155876345_155948769 | VAMP7 | chrX | 155876345 | 155948769 |
| g0005 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | VAMP7_chrX_155876345_155948769 | VAMP7 | chrX | 155876345 | 155948769 |
| g0006 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | VAMP7_chrX_155876345_155948769 | VAMP7 | chrX | 155876345 | 155948769 |
| g0007 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | VAMP7_chrX_155876345_155948769 | VAMP7 | chrX | 155876345 | 155948769 |
| g0008 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | VAMP7_chrX_155876345_155948769 | VAMP7 | chrX | 155876345 | 155948769 |
| g0009 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | VAMP7_chrX_155876345_155948769 | VAMP7 | chrX | 155876345 | 155948769 |
| g0010 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | VAMP7_chrX_155876345_155948769 | VAMP7 | chrX | 155876345 | 155948769 |
| g0011 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | VAMP7_chrX_155876345_155948769 | VAMP7 | chrX | 155876345 | 155948769 |
| g0012 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | VAMP7_chrX_155876345_155948769 | VAMP7 | chrX | 155876345 | 155948769 |
| g0013 | 0/0 | 2 | 0 | 0 | 1 | 1 | 0 | VAMP7_chrX_155876345_155948769 | VAMP7 | chrX | 155876345 | 155948769 |
| g0014 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | VAMP7_chrX_155876345_155948769 | VAMP7 | chrX | 155876345 | 155948769 |
| g0015 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | VAMP7_chrX_155876345_155948769 | VAMP7 | chrX | 155876345 | 155948769 |
| g0016 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | VAMP7_chrX_155876345_155948769 | VAMP7 | chrX | 155876345 | 155948769 |
| g0017 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | VAMP7_chrX_155876345_155948769 | VAMP7 | chrX | 155876345 | 155948769 |
| g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VAMP7_chrX_155876345_155948769 | VAMP7 | chrX | 155876345 | 155948769 |
| g0019 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VAMP7_chrX_155876345_155948769 | VAMP7 | chrX | 155876345 | 155948769 |
| g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VAMP7_chrX_155876345_155948769 | VAMP7 | chrX | 155876345 | 155948769 |
| g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VAMP7_chrX_155876345_155948769 | VAMP7 | chrX | 155876345 | 155948769 |
| g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VAMP7_chrX_155876345_155948769 | VAMP7 | chrX | 155876345 | 155948769 |
| g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VAMP7_chrX_155876345_155948769 | VAMP7 | chrX | 155876345 | 155948769 |
| g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VAMP7_chrX_155876345_155948769 | VAMP7 | chrX | 155876345 | 155948769 |
| g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VAMP7_chrX_155876345_155948769 | VAMP7 | chrX | 155876345 | 155948769 |
| g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VAMP7_chrX_155876345_155948769 | VAMP7 | chrX | 155876345 | 155948769 |
| g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VAMP7_chrX_155876345_155948769 | VAMP7 | chrX | 155876345 | 155948769 |
| g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VAMP7_chrX_155876345_155948769 | VAMP7 | chrX | 155876345 | 155948769 |
| g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VAMP7_chrX_155876345_155948769 | VAMP7 | chrX | 155876345 | 155948769 |
| g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VAMP7_chrX_155876345_155948769 | VAMP7 | chrX | 155876345 | 155948769 |
| g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VAMP7_chrX_155876345_155948769 | VAMP7 | chrX | 155876345 | 155948769 |
| g0032 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | VAMP7_chrX_155876345_155948769 | VAMP7 | chrX | 155876345 | 155948769 |
| g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VAMP7_chrX_155876345_155948769 | VAMP7 | chrX | 155876345 | 155948769 |
| g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VAMP7_chrX_155876345_155948769 | VAMP7 | chrX | 155876345 | 155948769 |
| g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VAMP7_chrX_155876345_155948769 | VAMP7 | chrX | 155876345 | 155948769 |
| g0036 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VAMP7_chrX_155876345_155948769 | VAMP7 | chrX | 155876345 | 155948769 |
| g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VAMP7_chrX_155876345_155948769 | VAMP7 | chrX | 155876345 | 155948769 |
| g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VAMP7_chrX_155876345_155948769 | VAMP7 | chrX | 155876345 | 155948769 |
| g0039 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VAMP7_chrX_155876345_155948769 | VAMP7 | chrX | 155876345 | 155948769 |
| g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VAMP7_chrX_155876345_155948769 | VAMP7 | chrX | 155876345 | 155948769 |
| g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VAMP7_chrX_155876345_155948769 | VAMP7 | chrX | 155876345 | 155948769 |
| g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VAMP7_chrX_155876345_155948769 | VAMP7 | chrX | 155876345 | 155948769 |
| g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VAMP7_chrX_155876345_155948769 | VAMP7 | chrX | 155876345 | 155948769 |
| g0044 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VAMP7_chrX_155876345_155948769 | VAMP7 | chrX | 155876345 | 155948769 |
| g0045 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | VAMP7_chrX_155876345_155948769 | VAMP7 | chrX | 155876345 | 155948769 |
| g0046 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | VAMP7_chrX_155876345_155948769 | VAMP7 | chrX | 155876345 | 155948769 |
| g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VAMP7_chrX_155876345_155948769 | VAMP7 | chrX | 155876345 | 155948769 |
| g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VAMP7_chrX_155876345_155948769 | VAMP7 | chrX | 155876345 | 155948769 |
| g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VAMP7_chrX_155876345_155948769 | VAMP7 | chrX | 155876345 | 155948769 |
| g0050 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | VAMP7_chrX_155876345_155948769 | VAMP7 | chrX | 155876345 | 155948769 |
| g0051 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | VAMP7_chrX_155876345_155948769 | VAMP7 | chrX | 155876345 | 155948769 |
| g0052 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VAMP7_chrX_155876345_155948769 | VAMP7 | chrX | 155876345 | 155948769 |
| g0053 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | VAMP7_chrX_155876345_155948769 | VAMP7 | chrX | 155876345 | 155948769 |
| g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VAMP7_chrX_155876345_155948769 | VAMP7 | chrX | 155876345 | 155948769 |
| g0055 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VAMP7_chrX_155876345_155948769 | VAMP7 | chrX | 155876345 | 155948769 |
| g0056 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VAMP7_chrX_155876345_155948769 | VAMP7 | chrX | 155876345 | 155948769 |
| g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VAMP7_chrX_155876345_155948769 | VAMP7 | chrX | 155876345 | 155948769 |
| g0058 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | VAMP7_chrX_155876345_155948769 | VAMP7 | chrX | 155876345 | 155948769 |
| g0059 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VAMP7_chrX_155876345_155948769 | VAMP7 | chrX | 155876345 | 155948769 |
| g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VAMP7_chrX_155876345_155948769 | VAMP7 | chrX | 155876345 | 155948769 |
| g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VAMP7_chrX_155876345_155948769 | VAMP7 | chrX | 155876345 | 155948769 |
| g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VAMP7_chrX_155876345_155948769 | VAMP7 | chrX | 155876345 | 155948769 |
| g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VAMP7_chrX_155876345_155948769 | VAMP7 | chrX | 155876345 | 155948769 |
| g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VAMP7_chrX_155876345_155948769 | VAMP7 | chrX | 155876345 | 155948769 |
| g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VAMP7_chrX_155876345_155948769 | VAMP7 | chrX | 155876345 | 155948769 |
| g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VAMP7_chrX_155876345_155948769 | VAMP7 | chrX | 155876345 | 155948769 |
| g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VAMP7_chrX_155876345_155948769 | VAMP7 | chrX | 155876345 | 155948769 |
| g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VAMP7_chrX_155876345_155948769 | VAMP7 | chrX | 155876345 | 155948769 |
| g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VAMP7_chrX_155876345_155948769 | VAMP7 | chrX | 155876345 | 155948769 |
| g0070 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VAMP7_chrX_155876345_155948769 | VAMP7 | chrX | 155876345 | 155948769 |
| g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VAMP7_chrX_155876345_155948769 | VAMP7 | chrX | 155876345 | 155948769 |
| g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VAMP7_chrX_155876345_155948769 | VAMP7 | chrX | 155876345 | 155948769 |
| g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VAMP7_chrX_155876345_155948769 | VAMP7 | chrX | 155876345 | 155948769 |
| g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VAMP7_chrX_155876345_155948769 | VAMP7 | chrX | 155876345 | 155948769 |
| g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VAMP7_chrX_155876345_155948769 | VAMP7 | chrX | 155876345 | 155948769 |
| g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VAMP7_chrX_155876345_155948769 | VAMP7 | chrX | 155876345 | 155948769 |
| g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VAMP7_chrX_155876345_155948769 | VAMP7 | chrX | 155876345 | 155948769 |
| g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VAMP7_chrX_155876345_155948769 | VAMP7 | chrX | 155876345 | 155948769 |
| g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VAMP7_chrX_155876345_155948769 | VAMP7 | chrX | 155876345 | 155948769 |
| g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VAMP7_chrX_155876345_155948769 | VAMP7 | chrX | 155876345 | 155948769 |
| g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VAMP7_chrX_155876345_155948769 | VAMP7 | chrX | 155876345 | 155948769 |
| g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VAMP7_chrX_155876345_155948769 | VAMP7 | chrX | 155876345 | 155948769 |
| g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VAMP7_chrX_155876345_155948769 | VAMP7 | chrX | 155876345 | 155948769 |
| g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VAMP7_chrX_155876345_155948769 | VAMP7 | chrX | 155876345 | 155948769 |
| g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VAMP7_chrX_155876345_155948769 | VAMP7 | chrX | 155876345 | 155948769 |
| g0086 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VAMP7_chrX_155876345_155948769 | VAMP7 | chrX | 155876345 | 155948769 |
| g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VAMP7_chrX_155876345_155948769 | VAMP7 | chrX | 155876345 | 155948769 |
| g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VAMP7_chrX_155876345_155948769 | VAMP7 | chrX | 155876345 | 155948769 |
| g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VAMP7_chrX_155876345_155948769 | VAMP7 | chrX | 155876345 | 155948769 |
| g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VAMP7_chrX_155876345_155948769 | VAMP7 | chrX | 155876345 | 155948769 |
| g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VAMP7_chrX_155876345_155948769 | VAMP7 | chrX | 155876345 | 155948769 |
| g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VAMP7_chrX_155876345_155948769 | VAMP7 | chrX | 155876345 | 155948769 |
| g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VAMP7_chrX_155876345_155948769 | VAMP7 | chrX | 155876345 | 155948769 |
| g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VAMP7_chrX_155876345_155948769 | VAMP7 | chrX | 155876345 | 155948769 |
| g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VAMP7_chrX_155876345_155948769 | VAMP7 | chrX | 155876345 | 155948769 |
| g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VAMP7_chrX_155876345_155948769 | VAMP7 | chrX | 155876345 | 155948769 |
| g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VAMP7_chrX_155876345_155948769 | VAMP7 | chrX | 155876345 | 155948769 |
| g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VAMP7_chrX_155876345_155948769 | VAMP7 | chrX | 155876345 | 155948769 |
| g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VAMP7_chrX_155876345_155948769 | VAMP7 | chrX | 155876345 | 155948769 |
| g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VAMP7_chrX_155876345_155948769 | VAMP7 | chrX | 155876345 | 155948769 |
| g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VAMP7_chrX_155876345_155948769 | VAMP7 | chrX | 155876345 | 155948769 |
| g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VAMP7_chrX_155876345_155948769 | VAMP7 | chrX | 155876345 | 155948769 |
| g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VAMP7_chrX_155876345_155948769 | VAMP7 | chrX | 155876345 | 155948769 |
| g0104 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VAMP7_chrX_155876345_155948769 | VAMP7 | chrX | 155876345 | 155948769 |
| g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VAMP7_chrX_155876345_155948769 | VAMP7 | chrX | 155876345 | 155948769 |
| g0106 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VAMP7_chrX_155876345_155948769 | VAMP7 | chrX | 155876345 | 155948769 |
| g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VAMP7_chrX_155876345_155948769 | VAMP7 | chrX | 155876345 | 155948769 |
| g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VAMP7_chrX_155876345_155948769 | VAMP7 | chrX | 155876345 | 155948769 |
| g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VAMP7_chrX_155876345_155948769 | VAMP7 | chrX | 155876345 | 155948769 |
| g0110 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VAMP7_chrX_155876345_155948769 | VAMP7 | chrX | 155876345 | 155948769 |
| g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VAMP7_chrX_155876345_155948769 | VAMP7 | chrX | 155876345 | 155948769 |
| g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VAMP7_chrX_155876345_155948769 | VAMP7 | chrX | 155876345 | 155948769 |
| g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VAMP7_chrX_155876345_155948769 | VAMP7 | chrX | 155876345 | 155948769 |
| g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VAMP7_chrX_155876345_155948769 | VAMP7 | chrX | 155876345 | 155948769 |
| g0115 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | VAMP7_chrX_155876345_155948769 | VAMP7 | chrX | 155876345 | 155948769 |
| g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VAMP7_chrX_155876345_155948769 | VAMP7 | chrX | 155876345 | 155948769 |
| g0117 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | VAMP7_chrX_155876345_155948769 | VAMP7 | chrX | 155876345 | 155948769 |
| g0118 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VAMP7_chrX_155876345_155948769 | VAMP7 | chrX | 155876345 | 155948769 |
| g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VAMP7_chrX_155876345_155948769 | VAMP7 | chrX | 155876345 | 155948769 |
| g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VAMP7_chrX_155876345_155948769 | VAMP7 | chrX | 155876345 | 155948769 |
| g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VAMP7_chrX_155876345_155948769 | VAMP7 | chrX | 155876345 | 155948769 |
| g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VAMP7_chrX_155876345_155948769 | VAMP7 | chrX | 155876345 | 155948769 |
| g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VAMP7_chrX_155876345_155948769 | VAMP7 | chrX | 155876345 | 155948769 |
| g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VAMP7_chrX_155876345_155948769 | VAMP7 | chrX | 155876345 | 155948769 |
| g0125 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VAMP7_chrX_155876345_155948769 | VAMP7 | chrX | 155876345 | 155948769 |
| g0126 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VAMP7_chrX_155876345_155948769 | VAMP7 | chrX | 155876345 | 155948769 |
| g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VAMP7_chrX_155876345_155948769 | VAMP7 | chrX | 155876345 | 155948769 |
| g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VAMP7_chrX_155876345_155948769 | VAMP7 | chrX | 155876345 | 155948769 |
| g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VAMP7_chrX_155876345_155948769 | VAMP7 | chrX | 155876345 | 155948769 |
| g0130 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VAMP7_chrX_155876345_155948769 | VAMP7 | chrX | 155876345 | 155948769 |
| g0131 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VAMP7_chrX_155876345_155948769 | VAMP7 | chrX | 155876345 | 155948769 |
| g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VAMP7_chrX_155876345_155948769 | VAMP7 | chrX | 155876345 | 155948769 |
| g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VAMP7_chrX_155876345_155948769 | VAMP7 | chrX | 155876345 | 155948769 |
| g0134 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VAMP7_chrX_155876345_155948769 | VAMP7 | chrX | 155876345 | 155948769 |
| g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VAMP7_chrX_155876345_155948769 | VAMP7 | chrX | 155876345 | 155948769 |
| g0136 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VAMP7_chrX_155876345_155948769 | VAMP7 | chrX | 155876345 | 155948769 |
| g0137 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VAMP7_chrX_155876345_155948769 | VAMP7 | chrX | 155876345 | 155948769 |
| g0138 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | VAMP7_chrX_155876345_155948769 | VAMP7 | chrX | 155876345 | 155948769 |
| g0139 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | VAMP7_chrX_155876345_155948769 | VAMP7 | chrX | 155876345 | 155948769 |
| g0140 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VAMP7_chrX_155876345_155948769 | VAMP7 | chrX | 155876345 | 155948769 |
| g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VAMP7_chrX_155876345_155948769 | VAMP7 | chrX | 155876345 | 155948769 |
| g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VAMP7_chrX_155876345_155948769 | VAMP7 | chrX | 155876345 | 155948769 |
| g0143 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | VAMP7_chrX_155876345_155948769 | VAMP7 | chrX | 155876345 | 155948769 |
| g0144 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VAMP7_chrX_155876345_155948769 | VAMP7 | chrX | 155876345 | 155948769 |
| g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VAMP7_chrX_155876345_155948769 | VAMP7 | chrX | 155876345 | 155948769 |
| g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VAMP7_chrX_155876345_155948769 | VAMP7 | chrX | 155876345 | 155948769 |
| g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VAMP7_chrX_155876345_155948769 | VAMP7 | chrX | 155876345 | 155948769 |
| g0148 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | VAMP7_chrX_155876345_155948769 | VAMP7 | chrX | 155876345 | 155948769 |
| g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VAMP7_chrX_155876345_155948769 | VAMP7 | chrX | 155876345 | 155948769 |
| g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VAMP7_chrX_155876345_155948769 | VAMP7 | chrX | 155876345 | 155948769 |
| g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VAMP7_chrX_155876345_155948769 | VAMP7 | chrX | 155876345 | 155948769 |
| g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VAMP7_chrX_155876345_155948769 | VAMP7 | chrX | 155876345 | 155948769 |
| g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VAMP7_chrX_155876345_155948769 | VAMP7 | chrX | 155876345 | 155948769 |
| g0154 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VAMP7_chrX_155876345_155948769 | VAMP7 | chrX | 155876345 | 155948769 |
| g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VAMP7_chrX_155876345_155948769 | VAMP7 | chrX | 155876345 | 155948769 |
| g0156 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | VAMP7_chrX_155876345_155948769 | VAMP7 | chrX | 155876345 | 155948769 |
| g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VAMP7_chrX_155876345_155948769 | VAMP7 | chrX | 155876345 | 155948769 |
| g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VAMP7_chrX_155876345_155948769 | VAMP7 | chrX | 155876345 | 155948769 |
| g0159 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | VAMP7_chrX_155876345_155948769 | VAMP7 | chrX | 155876345 | 155948769 |
| achapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 663 | 181 | 56 | 34 | 73 | 6 | 10 | VAMP7_chrX_155876345_155948769 | VAMP7 | copy fasta | chrX | 155876345 | 155948769 |
| a0001c0002 | 0/0 | 663 | 3 | 3 | 0 | 0 | 0 | 0 | VAMP7_chrX_155876345_155948769 | VAMP7 | copy fasta | chrX | 155876345 | 155948769 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 1/1 | 2594 | 159 | 52 | 24 | 69 | 3 | 9 | VAMP7_chrX_155876345_155948769 | VAMP7 | copy fasta | chrX | 155876345 | 155948769 |
| a0001c0001t0002 | 0/0 | 2594 | 17 | 1 | 10 | 2 | 3 | 1 | VAMP7_chrX_155876345_155948769 | VAMP7 | copy fasta | chrX | 155876345 | 155948769 |
| a0001c0001t0003 | 0/0 | 2594 | 1 | 1 | 0 | 0 | 0 | 0 | VAMP7_chrX_155876345_155948769 | VAMP7 | copy fasta | chrX | 155876345 | 155948769 |
| a0001c0001t0004 | 0/0 | 2594 | 1 | 1 | 0 | 0 | 0 | 0 | VAMP7_chrX_155876345_155948769 | VAMP7 | copy fasta | chrX | 155876345 | 155948769 |
| a0001c0001t0005 | 0/0 | 2594 | 1 | 0 | 0 | 1 | 0 | 0 | VAMP7_chrX_155876345_155948769 | VAMP7 | copy fasta | chrX | 155876345 | 155948769 |
| a0001c0001t0006 | 0/0 | 2594 | 1 | 1 | 0 | 0 | 0 | 0 | VAMP7_chrX_155876345_155948769 | VAMP7 | copy fasta | chrX | 155876345 | 155948769 |
| a0001c0001t0007 | 0/0 | 2594 | 1 | 0 | 0 | 1 | 0 | 0 | VAMP7_chrX_155876345_155948769 | VAMP7 | copy fasta | chrX | 155876345 | 155948769 |
| a0001c0002t0001 | 0/0 | 2594 | 3 | 3 | 0 | 0 | 0 | 0 | VAMP7_chrX_155876345_155948769 | VAMP7 | copy fasta | chrX | 155876345 | 155948769 |
| actghapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | VAMP7_chrX_155876345_155948769 | VAMP7 | chrX | 155876345 | 155948769 |
| a0001c0001t0001g0002 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | VAMP7_chrX_155876345_155948769 | VAMP7 | chrX | 155876345 | 155948769 |
| a0001c0001t0001g0004 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | VAMP7_chrX_155876345_155948769 | VAMP7 | chrX | 155876345 | 155948769 |
| a0001c0001t0001g0005 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | VAMP7_chrX_155876345_155948769 | VAMP7 | chrX | 155876345 | 155948769 |
| a0001c0001t0001g0007 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | VAMP7_chrX_155876345_155948769 | VAMP7 | chrX | 155876345 | 155948769 |
| a0001c0001t0001g0008 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | VAMP7_chrX_155876345_155948769 | VAMP7 | chrX | 155876345 | 155948769 |
| a0001c0001t0001g0009 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | VAMP7_chrX_155876345_155948769 | VAMP7 | chrX | 155876345 | 155948769 |
| a0001c0001t0001g0010 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | VAMP7_chrX_155876345_155948769 | VAMP7 | chrX | 155876345 | 155948769 |
| a0001c0001t0001g0011 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | VAMP7_chrX_155876345_155948769 | VAMP7 | chrX | 155876345 | 155948769 |
| a0001c0001t0001g0012 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | VAMP7_chrX_155876345_155948769 | VAMP7 | chrX | 155876345 | 155948769 |
| a0001c0001t0001g0013 | 0/0 | 2 | 0 | 0 | 1 | 1 | 0 | VAMP7_chrX_155876345_155948769 | VAMP7 | chrX | 155876345 | 155948769 |
| a0001c0001t0001g0014 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | VAMP7_chrX_155876345_155948769 | VAMP7 | chrX | 155876345 | 155948769 |
| a0001c0001t0001g0015 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | VAMP7_chrX_155876345_155948769 | VAMP7 | chrX | 155876345 | 155948769 |
| a0001c0001t0001g0016 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | VAMP7_chrX_155876345_155948769 | VAMP7 | chrX | 155876345 | 155948769 |
| a0001c0001t0001g0019 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VAMP7_chrX_155876345_155948769 | VAMP7 | chrX | 155876345 | 155948769 |
| a0001c0001t0001g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VAMP7_chrX_155876345_155948769 | VAMP7 | chrX | 155876345 | 155948769 |
| a0001c0001t0001g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VAMP7_chrX_155876345_155948769 | VAMP7 | chrX | 155876345 | 155948769 |
| a0001c0001t0001g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VAMP7_chrX_155876345_155948769 | VAMP7 | chrX | 155876345 | 155948769 |
| a0001c0001t0001g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VAMP7_chrX_155876345_155948769 | VAMP7 | chrX | 155876345 | 155948769 |
| a0001c0001t0001g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VAMP7_chrX_155876345_155948769 | VAMP7 | chrX | 155876345 | 155948769 |
| a0001c0001t0001g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VAMP7_chrX_155876345_155948769 | VAMP7 | chrX | 155876345 | 155948769 |
| a0001c0001t0001g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VAMP7_chrX_155876345_155948769 | VAMP7 | chrX | 155876345 | 155948769 |
| a0001c0001t0001g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VAMP7_chrX_155876345_155948769 | VAMP7 | chrX | 155876345 | 155948769 |
| a0001c0001t0001g0032 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | VAMP7_chrX_155876345_155948769 | VAMP7 | chrX | 155876345 | 155948769 |
| a0001c0001t0001g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VAMP7_chrX_155876345_155948769 | VAMP7 | chrX | 155876345 | 155948769 |
| a0001c0001t0001g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VAMP7_chrX_155876345_155948769 | VAMP7 | chrX | 155876345 | 155948769 |
| a0001c0001t0001g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VAMP7_chrX_155876345_155948769 | VAMP7 | chrX | 155876345 | 155948769 |
| a0001c0001t0001g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VAMP7_chrX_155876345_155948769 | VAMP7 | chrX | 155876345 | 155948769 |
| a0001c0001t0001g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VAMP7_chrX_155876345_155948769 | VAMP7 | chrX | 155876345 | 155948769 |
| a0001c0001t0001g0039 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VAMP7_chrX_155876345_155948769 | VAMP7 | chrX | 155876345 | 155948769 |
| a0001c0001t0001g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VAMP7_chrX_155876345_155948769 | VAMP7 | chrX | 155876345 | 155948769 |
| a0001c0001t0001g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VAMP7_chrX_155876345_155948769 | VAMP7 | chrX | 155876345 | 155948769 |
| a0001c0001t0001g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VAMP7_chrX_155876345_155948769 | VAMP7 | chrX | 155876345 | 155948769 |
| a0001c0001t0001g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VAMP7_chrX_155876345_155948769 | VAMP7 | chrX | 155876345 | 155948769 |
| a0001c0001t0001g0044 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VAMP7_chrX_155876345_155948769 | VAMP7 | chrX | 155876345 | 155948769 |
| a0001c0001t0001g0045 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | VAMP7_chrX_155876345_155948769 | VAMP7 | chrX | 155876345 | 155948769 |
| a0001c0001t0001g0046 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | VAMP7_chrX_155876345_155948769 | VAMP7 | chrX | 155876345 | 155948769 |
| a0001c0001t0001g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VAMP7_chrX_155876345_155948769 | VAMP7 | chrX | 155876345 | 155948769 |
| a0001c0001t0001g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VAMP7_chrX_155876345_155948769 | VAMP7 | chrX | 155876345 | 155948769 |
| a0001c0001t0001g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VAMP7_chrX_155876345_155948769 | VAMP7 | chrX | 155876345 | 155948769 |
| a0001c0001t0001g0050 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | VAMP7_chrX_155876345_155948769 | VAMP7 | chrX | 155876345 | 155948769 |
| a0001c0001t0001g0051 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | VAMP7_chrX_155876345_155948769 | VAMP7 | chrX | 155876345 | 155948769 |
| a0001c0001t0001g0052 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VAMP7_chrX_155876345_155948769 | VAMP7 | chrX | 155876345 | 155948769 |
| a0001c0001t0001g0053 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | VAMP7_chrX_155876345_155948769 | VAMP7 | chrX | 155876345 | 155948769 |
| a0001c0001t0001g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VAMP7_chrX_155876345_155948769 | VAMP7 | chrX | 155876345 | 155948769 |
| a0001c0001t0001g0055 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VAMP7_chrX_155876345_155948769 | VAMP7 | chrX | 155876345 | 155948769 |
| a0001c0001t0001g0056 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VAMP7_chrX_155876345_155948769 | VAMP7 | chrX | 155876345 | 155948769 |
| a0001c0001t0001g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VAMP7_chrX_155876345_155948769 | VAMP7 | chrX | 155876345 | 155948769 |
| a0001c0001t0001g0058 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | VAMP7_chrX_155876345_155948769 | VAMP7 | chrX | 155876345 | 155948769 |
| a0001c0001t0001g0059 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VAMP7_chrX_155876345_155948769 | VAMP7 | chrX | 155876345 | 155948769 |
| a0001c0001t0001g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VAMP7_chrX_155876345_155948769 | VAMP7 | chrX | 155876345 | 155948769 |
| a0001c0001t0001g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VAMP7_chrX_155876345_155948769 | VAMP7 | chrX | 155876345 | 155948769 |
| a0001c0001t0001g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VAMP7_chrX_155876345_155948769 | VAMP7 | chrX | 155876345 | 155948769 |
| a0001c0001t0001g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VAMP7_chrX_155876345_155948769 | VAMP7 | chrX | 155876345 | 155948769 |
| a0001c0001t0001g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VAMP7_chrX_155876345_155948769 | VAMP7 | chrX | 155876345 | 155948769 |
| a0001c0001t0001g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VAMP7_chrX_155876345_155948769 | VAMP7 | chrX | 155876345 | 155948769 |
| a0001c0001t0001g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VAMP7_chrX_155876345_155948769 | VAMP7 | chrX | 155876345 | 155948769 |
| a0001c0001t0001g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VAMP7_chrX_155876345_155948769 | VAMP7 | chrX | 155876345 | 155948769 |
| a0001c0001t0001g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VAMP7_chrX_155876345_155948769 | VAMP7 | chrX | 155876345 | 155948769 |
| a0001c0001t0001g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VAMP7_chrX_155876345_155948769 | VAMP7 | chrX | 155876345 | 155948769 |
| a0001c0001t0001g0070 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VAMP7_chrX_155876345_155948769 | VAMP7 | chrX | 155876345 | 155948769 |
| a0001c0001t0001g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VAMP7_chrX_155876345_155948769 | VAMP7 | chrX | 155876345 | 155948769 |
| a0001c0001t0001g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VAMP7_chrX_155876345_155948769 | VAMP7 | chrX | 155876345 | 155948769 |
| a0001c0001t0001g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VAMP7_chrX_155876345_155948769 | VAMP7 | chrX | 155876345 | 155948769 |
| a0001c0001t0001g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VAMP7_chrX_155876345_155948769 | VAMP7 | chrX | 155876345 | 155948769 |
| a0001c0001t0001g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VAMP7_chrX_155876345_155948769 | VAMP7 | chrX | 155876345 | 155948769 |
| a0001c0001t0001g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VAMP7_chrX_155876345_155948769 | VAMP7 | chrX | 155876345 | 155948769 |
| a0001c0001t0001g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VAMP7_chrX_155876345_155948769 | VAMP7 | chrX | 155876345 | 155948769 |
| a0001c0001t0001g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VAMP7_chrX_155876345_155948769 | VAMP7 | chrX | 155876345 | 155948769 |
| a0001c0001t0001g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VAMP7_chrX_155876345_155948769 | VAMP7 | chrX | 155876345 | 155948769 |
| a0001c0001t0001g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VAMP7_chrX_155876345_155948769 | VAMP7 | chrX | 155876345 | 155948769 |
| a0001c0001t0001g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VAMP7_chrX_155876345_155948769 | VAMP7 | chrX | 155876345 | 155948769 |
| a0001c0001t0001g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VAMP7_chrX_155876345_155948769 | VAMP7 | chrX | 155876345 | 155948769 |
| a0001c0001t0001g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VAMP7_chrX_155876345_155948769 | VAMP7 | chrX | 155876345 | 155948769 |
| a0001c0001t0001g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VAMP7_chrX_155876345_155948769 | VAMP7 | chrX | 155876345 | 155948769 |
| a0001c0001t0001g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VAMP7_chrX_155876345_155948769 | VAMP7 | chrX | 155876345 | 155948769 |
| a0001c0001t0001g0086 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VAMP7_chrX_155876345_155948769 | VAMP7 | chrX | 155876345 | 155948769 |
| a0001c0001t0001g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VAMP7_chrX_155876345_155948769 | VAMP7 | chrX | 155876345 | 155948769 |
| a0001c0001t0001g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VAMP7_chrX_155876345_155948769 | VAMP7 | chrX | 155876345 | 155948769 |
| a0001c0001t0001g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VAMP7_chrX_155876345_155948769 | VAMP7 | chrX | 155876345 | 155948769 |
| a0001c0001t0001g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VAMP7_chrX_155876345_155948769 | VAMP7 | chrX | 155876345 | 155948769 |
| a0001c0001t0001g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VAMP7_chrX_155876345_155948769 | VAMP7 | chrX | 155876345 | 155948769 |
| a0001c0001t0001g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VAMP7_chrX_155876345_155948769 | VAMP7 | chrX | 155876345 | 155948769 |
| a0001c0001t0001g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VAMP7_chrX_155876345_155948769 | VAMP7 | chrX | 155876345 | 155948769 |
| a0001c0001t0001g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VAMP7_chrX_155876345_155948769 | VAMP7 | chrX | 155876345 | 155948769 |
| a0001c0001t0001g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VAMP7_chrX_155876345_155948769 | VAMP7 | chrX | 155876345 | 155948769 |
| a0001c0001t0001g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VAMP7_chrX_155876345_155948769 | VAMP7 | chrX | 155876345 | 155948769 |
| a0001c0001t0001g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VAMP7_chrX_155876345_155948769 | VAMP7 | chrX | 155876345 | 155948769 |
| a0001c0001t0001g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VAMP7_chrX_155876345_155948769 | VAMP7 | chrX | 155876345 | 155948769 |
| a0001c0001t0001g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VAMP7_chrX_155876345_155948769 | VAMP7 | chrX | 155876345 | 155948769 |
| a0001c0001t0001g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VAMP7_chrX_155876345_155948769 | VAMP7 | chrX | 155876345 | 155948769 |
| a0001c0001t0001g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VAMP7_chrX_155876345_155948769 | VAMP7 | chrX | 155876345 | 155948769 |
| a0001c0001t0001g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VAMP7_chrX_155876345_155948769 | VAMP7 | chrX | 155876345 | 155948769 |
| a0001c0001t0001g0104 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VAMP7_chrX_155876345_155948769 | VAMP7 | chrX | 155876345 | 155948769 |
| a0001c0001t0001g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VAMP7_chrX_155876345_155948769 | VAMP7 | chrX | 155876345 | 155948769 |
| a0001c0001t0001g0106 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VAMP7_chrX_155876345_155948769 | VAMP7 | chrX | 155876345 | 155948769 |
| a0001c0001t0001g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VAMP7_chrX_155876345_155948769 | VAMP7 | chrX | 155876345 | 155948769 |
| a0001c0001t0001g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VAMP7_chrX_155876345_155948769 | VAMP7 | chrX | 155876345 | 155948769 |
| a0001c0001t0001g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VAMP7_chrX_155876345_155948769 | VAMP7 | chrX | 155876345 | 155948769 |
| a0001c0001t0001g0110 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VAMP7_chrX_155876345_155948769 | VAMP7 | chrX | 155876345 | 155948769 |
| a0001c0001t0001g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VAMP7_chrX_155876345_155948769 | VAMP7 | chrX | 155876345 | 155948769 |
| a0001c0001t0001g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VAMP7_chrX_155876345_155948769 | VAMP7 | chrX | 155876345 | 155948769 |
| a0001c0001t0001g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VAMP7_chrX_155876345_155948769 | VAMP7 | chrX | 155876345 | 155948769 |
| a0001c0001t0001g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VAMP7_chrX_155876345_155948769 | VAMP7 | chrX | 155876345 | 155948769 |
| a0001c0001t0001g0115 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | VAMP7_chrX_155876345_155948769 | VAMP7 | chrX | 155876345 | 155948769 |
| a0001c0001t0001g0117 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | VAMP7_chrX_155876345_155948769 | VAMP7 | chrX | 155876345 | 155948769 |
| a0001c0001t0001g0118 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VAMP7_chrX_155876345_155948769 | VAMP7 | chrX | 155876345 | 155948769 |
| a0001c0001t0001g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VAMP7_chrX_155876345_155948769 | VAMP7 | chrX | 155876345 | 155948769 |
| a0001c0001t0001g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VAMP7_chrX_155876345_155948769 | VAMP7 | chrX | 155876345 | 155948769 |
| a0001c0001t0001g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VAMP7_chrX_155876345_155948769 | VAMP7 | chrX | 155876345 | 155948769 |
| a0001c0001t0001g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VAMP7_chrX_155876345_155948769 | VAMP7 | chrX | 155876345 | 155948769 |
| a0001c0001t0001g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VAMP7_chrX_155876345_155948769 | VAMP7 | chrX | 155876345 | 155948769 |
| a0001c0001t0001g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VAMP7_chrX_155876345_155948769 | VAMP7 | chrX | 155876345 | 155948769 |
| a0001c0001t0001g0125 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VAMP7_chrX_155876345_155948769 | VAMP7 | chrX | 155876345 | 155948769 |
| a0001c0001t0001g0126 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VAMP7_chrX_155876345_155948769 | VAMP7 | chrX | 155876345 | 155948769 |
| a0001c0001t0001g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VAMP7_chrX_155876345_155948769 | VAMP7 | chrX | 155876345 | 155948769 |
| a0001c0001t0001g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VAMP7_chrX_155876345_155948769 | VAMP7 | chrX | 155876345 | 155948769 |
| a0001c0001t0001g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VAMP7_chrX_155876345_155948769 | VAMP7 | chrX | 155876345 | 155948769 |
| a0001c0001t0001g0130 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VAMP7_chrX_155876345_155948769 | VAMP7 | chrX | 155876345 | 155948769 |
| a0001c0001t0001g0131 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VAMP7_chrX_155876345_155948769 | VAMP7 | chrX | 155876345 | 155948769 |
| a0001c0001t0001g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VAMP7_chrX_155876345_155948769 | VAMP7 | chrX | 155876345 | 155948769 |
| a0001c0001t0001g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VAMP7_chrX_155876345_155948769 | VAMP7 | chrX | 155876345 | 155948769 |
| a0001c0001t0001g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VAMP7_chrX_155876345_155948769 | VAMP7 | chrX | 155876345 | 155948769 |
| a0001c0001t0001g0143 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | VAMP7_chrX_155876345_155948769 | VAMP7 | chrX | 155876345 | 155948769 |
| a0001c0001t0001g0144 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VAMP7_chrX_155876345_155948769 | VAMP7 | chrX | 155876345 | 155948769 |
| a0001c0001t0001g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VAMP7_chrX_155876345_155948769 | VAMP7 | chrX | 155876345 | 155948769 |
| a0001c0001t0001g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VAMP7_chrX_155876345_155948769 | VAMP7 | chrX | 155876345 | 155948769 |
| a0001c0001t0001g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VAMP7_chrX_155876345_155948769 | VAMP7 | chrX | 155876345 | 155948769 |
| a0001c0001t0001g0148 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | VAMP7_chrX_155876345_155948769 | VAMP7 | chrX | 155876345 | 155948769 |
| a0001c0001t0001g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VAMP7_chrX_155876345_155948769 | VAMP7 | chrX | 155876345 | 155948769 |
| a0001c0001t0001g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VAMP7_chrX_155876345_155948769 | VAMP7 | chrX | 155876345 | 155948769 |
| a0001c0001t0001g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VAMP7_chrX_155876345_155948769 | VAMP7 | chrX | 155876345 | 155948769 |
| a0001c0001t0001g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VAMP7_chrX_155876345_155948769 | VAMP7 | chrX | 155876345 | 155948769 |
| a0001c0001t0001g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VAMP7_chrX_155876345_155948769 | VAMP7 | chrX | 155876345 | 155948769 |
| a0001c0001t0001g0154 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VAMP7_chrX_155876345_155948769 | VAMP7 | chrX | 155876345 | 155948769 |
| a0001c0001t0001g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VAMP7_chrX_155876345_155948769 | VAMP7 | chrX | 155876345 | 155948769 |
| a0001c0001t0001g0156 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | VAMP7_chrX_155876345_155948769 | VAMP7 | chrX | 155876345 | 155948769 |
| a0001c0001t0001g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VAMP7_chrX_155876345_155948769 | VAMP7 | chrX | 155876345 | 155948769 |
| a0001c0001t0001g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VAMP7_chrX_155876345_155948769 | VAMP7 | chrX | 155876345 | 155948769 |
| a0001c0001t0001g0159 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | VAMP7_chrX_155876345_155948769 | VAMP7 | chrX | 155876345 | 155948769 |
| a0001c0001t0002g0003 | 0/0 | 3 | 1 | 1 | 0 | 1 | 0 | VAMP7_chrX_155876345_155948769 | VAMP7 | chrX | 155876345 | 155948769 |
| a0001c0001t0002g0006 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | VAMP7_chrX_155876345_155948769 | VAMP7 | chrX | 155876345 | 155948769 |
| a0001c0001t0002g0017 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | VAMP7_chrX_155876345_155948769 | VAMP7 | chrX | 155876345 | 155948769 |
| a0001c0001t0002g0036 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VAMP7_chrX_155876345_155948769 | VAMP7 | chrX | 155876345 | 155948769 |
| a0001c0001t0002g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VAMP7_chrX_155876345_155948769 | VAMP7 | chrX | 155876345 | 155948769 |
| a0001c0001t0002g0134 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VAMP7_chrX_155876345_155948769 | VAMP7 | chrX | 155876345 | 155948769 |
| a0001c0001t0002g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VAMP7_chrX_155876345_155948769 | VAMP7 | chrX | 155876345 | 155948769 |
| a0001c0001t0002g0136 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VAMP7_chrX_155876345_155948769 | VAMP7 | chrX | 155876345 | 155948769 |
| a0001c0001t0002g0137 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VAMP7_chrX_155876345_155948769 | VAMP7 | chrX | 155876345 | 155948769 |
| a0001c0001t0002g0138 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | VAMP7_chrX_155876345_155948769 | VAMP7 | chrX | 155876345 | 155948769 |
| a0001c0001t0002g0139 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | VAMP7_chrX_155876345_155948769 | VAMP7 | chrX | 155876345 | 155948769 |
| a0001c0001t0002g0140 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VAMP7_chrX_155876345_155948769 | VAMP7 | chrX | 155876345 | 155948769 |
| a0001c0001t0003g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VAMP7_chrX_155876345_155948769 | VAMP7 | chrX | 155876345 | 155948769 |
| a0001c0001t0004g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VAMP7_chrX_155876345_155948769 | VAMP7 | chrX | 155876345 | 155948769 |
| a0001c0001t0005g0001 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VAMP7_chrX_155876345_155948769 | VAMP7 | chrX | 155876345 | 155948769 |
| a0001c0001t0006g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VAMP7_chrX_155876345_155948769 | VAMP7 | chrX | 155876345 | 155948769 |
| a0001c0001t0007g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VAMP7_chrX_155876345_155948769 | VAMP7 | chrX | 155876345 | 155948769 |
| a0001c0002t0001g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VAMP7_chrX_155876345_155948769 | VAMP7 | chrX | 155876345 | 155948769 |
| a0001c0002t0001g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VAMP7_chrX_155876345_155948769 | VAMP7 | chrX | 155876345 | 155948769 |
| a0001c0002t0001g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VAMP7_chrX_155876345_155948769 | VAMP7 | chrX | 155876345 | 155948769 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0001 | g0013 | EUR | GBR | VAMP7_chrX_155876345_155948769 | VAMP7 | chrX | 155876345 | 155948769 |
| HG00099 | hp2 | a0001 | c0001 | t0002 | g0017 | EUR | GBR | VAMP7_chrX_155876345_155948769 | VAMP7 | chrX | 155876345 | 155948769 |
| HG00280 | hp1 | a0001 | c0001 | t0001 | g0148 | EUR | FIN | VAMP7_chrX_155876345_155948769 | VAMP7 | chrX | 155876345 | 155948769 |
| HG00408 | hp1 | a0001 | c0001 | t0001 | g0092 | EAS | CHS | VAMP7_chrX_155876345_155948769 | VAMP7 | chrX | 155876345 | 155948769 |
| HG00408 | hp2 | a0001 | c0001 | t0001 | g0121 | EAS | CHS | VAMP7_chrX_155876345_155948769 | VAMP7 | chrX | 155876345 | 155948769 |
| HG00558 | hp1 | a0001 | c0001 | t0001 | g0107 | EAS | CHS | VAMP7_chrX_155876345_155948769 | VAMP7 | chrX | 155876345 | 155948769 |
| HG00558 | hp2 | a0001 | c0001 | t0001 | g0132 | EAS | CHS | VAMP7_chrX_155876345_155948769 | VAMP7 | chrX | 155876345 | 155948769 |
| HG00597 | hp1 | a0001 | c0001 | t0001 | g0067 | EAS | CHS | VAMP7_chrX_155876345_155948769 | VAMP7 | chrX | 155876345 | 155948769 |
| HG00597 | hp2 | a0001 | c0001 | t0001 | g0114 | EAS | CHS | VAMP7_chrX_155876345_155948769 | VAMP7 | chrX | 155876345 | 155948769 |
| HG00621 | hp1 | a0001 | c0001 | t0001 | g0079 | EAS | CHS | VAMP7_chrX_155876345_155948769 | VAMP7 | chrX | 155876345 | 155948769 |
| HG00639 | hp1 | a0001 | c0001 | t0002 | g0006 | AMR | PUR | VAMP7_chrX_155876345_155948769 | VAMP7 | chrX | 155876345 | 155948769 |
| HG00639 | hp2 | a0001 | c0001 | t0001 | g0052 | AMR | PUR | VAMP7_chrX_155876345_155948769 | VAMP7 | chrX | 155876345 | 155948769 |
| HG00741 | hp1 | a0001 | c0001 | t0001 | g0059 | AMR | PUR | VAMP7_chrX_155876345_155948769 | VAMP7 | chrX | 155876345 | 155948769 |
| HG00741 | hp2 | a0001 | c0001 | t0001 | g0125 | AMR | PUR | VAMP7_chrX_155876345_155948769 | VAMP7 | chrX | 155876345 | 155948769 |
| HG01070 | hp1 | a0001 | c0001 | t0002 | g0036 | AMR | PUR | VAMP7_chrX_155876345_155948769 | VAMP7 | chrX | 155876345 | 155948769 |
| HG01070 | hp2 | a0001 | c0001 | t0001 | g0019 | AMR | PUR | VAMP7_chrX_155876345_155948769 | VAMP7 | chrX | 155876345 | 155948769 |
| HG01071 | hp1 | a0001 | c0001 | t0001 | g0055 | AMR | PUR | VAMP7_chrX_155876345_155948769 | VAMP7 | chrX | 155876345 | 155948769 |
| HG01071 | hp2 | a0001 | c0001 | t0002 | g0003 | AMR | PUR | VAMP7_chrX_155876345_155948769 | VAMP7 | chrX | 155876345 | 155948769 |
| HG01081 | hp1 | a0001 | c0001 | t0001 | g0056 | AMR | PUR | VAMP7_chrX_155876345_155948769 | VAMP7 | chrX | 155876345 | 155948769 |
| HG01081 | hp2 | a0001 | c0001 | t0001 | g0039 | AMR | PUR | VAMP7_chrX_155876345_155948769 | VAMP7 | chrX | 155876345 | 155948769 |
| HG01168 | hp1 | a0001 | c0001 | t0001 | g0008 | AMR | PUR | VAMP7_chrX_155876345_155948769 | VAMP7 | chrX | 155876345 | 155948769 |
| HG01168 | hp2 | a0001 | c0001 | t0001 | g0154 | AMR | PUR | VAMP7_chrX_155876345_155948769 | VAMP7 | chrX | 155876345 | 155948769 |
| HG01169 | hp1 | a0001 | c0001 | t0001 | g0008 | AMR | PUR | VAMP7_chrX_155876345_155948769 | VAMP7 | chrX | 155876345 | 155948769 |
| HG01169 | hp2 | a0001 | c0001 | t0001 | g0044 | AMR | PUR | VAMP7_chrX_155876345_155948769 | VAMP7 | chrX | 155876345 | 155948769 |
| HG01257 | hp1 | a0001 | c0001 | t0001 | g0104 | AMR | CLM | VAMP7_chrX_155876345_155948769 | VAMP7 | chrX | 155876345 | 155948769 |
| HG01257 | hp2 | a0001 | c0001 | t0002 | g0137 | AMR | CLM | VAMP7_chrX_155876345_155948769 | VAMP7 | chrX | 155876345 | 155948769 |
| HG01346 | hp1 | a0001 | c0001 | t0001 | g0144 | AMR | CLM | VAMP7_chrX_155876345_155948769 | VAMP7 | chrX | 155876345 | 155948769 |
| HG01346 | hp2 | a0001 | c0001 | t0001 | g0073 | AMR | CLM | VAMP7_chrX_155876345_155948769 | VAMP7 | chrX | 155876345 | 155948769 |
| HG01361 | hp1 | a0001 | c0001 | t0001 | g0118 | AMR | CLM | VAMP7_chrX_155876345_155948769 | VAMP7 | chrX | 155876345 | 155948769 |
| HG01361 | hp2 | a0001 | c0001 | t0001 | g0131 | AMR | CLM | VAMP7_chrX_155876345_155948769 | VAMP7 | chrX | 155876345 | 155948769 |
| HG01515 | hp1 | a0001 | c0001 | t0002 | g0139 | EUR | IBS | VAMP7_chrX_155876345_155948769 | VAMP7 | chrX | 155876345 | 155948769 |
| HG01517 | hp1 | a0001 | c0001 | t0001 | g0156 | EUR | IBS | VAMP7_chrX_155876345_155948769 | VAMP7 | chrX | 155876345 | 155948769 |
| HG01517 | hp2 | a0001 | c0001 | t0002 | g0003 | EUR | IBS | VAMP7_chrX_155876345_155948769 | VAMP7 | chrX | 155876345 | 155948769 |
| HG01884 | hp1 | a0001 | c0001 | t0001 | g0037 | AFR | ACB | VAMP7_chrX_155876345_155948769 | VAMP7 | chrX | 155876345 | 155948769 |
| HG01884 | hp2 | a0001 | c0001 | t0001 | g0042 | AFR | ACB | VAMP7_chrX_155876345_155948769 | VAMP7 | chrX | 155876345 | 155948769 |
| HG01891 | hp1 | a0001 | c0001 | t0001 | g0062 | AFR | ACB | VAMP7_chrX_155876345_155948769 | VAMP7 | chrX | 155876345 | 155948769 |
| HG01891 | hp2 | a0001 | c0001 | t0001 | g0119 | AFR | ACB | VAMP7_chrX_155876345_155948769 | VAMP7 | chrX | 155876345 | 155948769 |
| HG01928 | hp1 | a0001 | c0001 | t0002 | g0134 | AMR | PEL | VAMP7_chrX_155876345_155948769 | VAMP7 | chrX | 155876345 | 155948769 |
| HG01978 | hp1 | a0001 | c0001 | t0002 | g0140 | AMR | PEL | VAMP7_chrX_155876345_155948769 | VAMP7 | chrX | 155876345 | 155948769 |
| HG01978 | hp2 | a0001 | c0001 | t0001 | g0070 | AMR | PEL | VAMP7_chrX_155876345_155948769 | VAMP7 | chrX | 155876345 | 155948769 |
| HG01993 | hp1 | a0001 | c0001 | t0002 | g0006 | AMR | PEL | VAMP7_chrX_155876345_155948769 | VAMP7 | chrX | 155876345 | 155948769 |
| HG01993 | hp2 | a0001 | c0001 | t0001 | g0130 | AMR | PEL | VAMP7_chrX_155876345_155948769 | VAMP7 | chrX | 155876345 | 155948769 |
| HG02004 | hp1 | a0001 | c0001 | t0002 | g0006 | AMR | PEL | VAMP7_chrX_155876345_155948769 | VAMP7 | chrX | 155876345 | 155948769 |
| HG02004 | hp2 | a0001 | c0001 | t0001 | g0009 | AMR | PEL | VAMP7_chrX_155876345_155948769 | VAMP7 | chrX | 155876345 | 155948769 |
| HG02083 | hp1 | a0001 | c0001 | t0001 | g0098 | EAS | KHV | VAMP7_chrX_155876345_155948769 | VAMP7 | chrX | 155876345 | 155948769 |
| HG02132 | hp2 | a0001 | c0001 | t0001 | g0021 | EAS | KHV | VAMP7_chrX_155876345_155948769 | VAMP7 | chrX | 155876345 | 155948769 |
| HG02148 | hp1 | a0001 | c0001 | t0001 | g0110 | AMR | PEL | VAMP7_chrX_155876345_155948769 | VAMP7 | chrX | 155876345 | 155948769 |
| HG02148 | hp2 | a0001 | c0001 | t0002 | g0136 | AMR | PEL | VAMP7_chrX_155876345_155948769 | VAMP7 | chrX | 155876345 | 155948769 |
| HG02155 | hp1 | a0001 | c0001 | t0001 | g0057 | EAS | CDX | VAMP7_chrX_155876345_155948769 | VAMP7 | chrX | 155876345 | 155948769 |
| HG02155 | hp2 | a0001 | c0001 | t0002 | g0133 | EAS | CDX | VAMP7_chrX_155876345_155948769 | VAMP7 | chrX | 155876345 | 155948769 |
| HG02165 | hp1 | a0001 | c0001 | t0001 | g0041 | EAS | CDX | VAMP7_chrX_155876345_155948769 | VAMP7 | chrX | 155876345 | 155948769 |
| HG02165 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | CDX | VAMP7_chrX_155876345_155948769 | VAMP7 | chrX | 155876345 | 155948769 |
| HG02257 | hp1 | a0001 | c0001 | t0001 | g0102 | AFR | ACB | VAMP7_chrX_155876345_155948769 | VAMP7 | chrX | 155876345 | 155948769 |
| HG02257 | hp2 | a0001 | c0001 | t0001 | g0007 | AFR | ACB | VAMP7_chrX_155876345_155948769 | VAMP7 | chrX | 155876345 | 155948769 |
| HG02280 | hp1 | a0001 | c0001 | t0001 | g0002 | AFR | ACB | VAMP7_chrX_155876345_155948769 | VAMP7 | chrX | 155876345 | 155948769 |
| HG02280 | hp2 | a0001 | c0001 | t0001 | g0100 | AFR | ACB | VAMP7_chrX_155876345_155948769 | VAMP7 | chrX | 155876345 | 155948769 |
| HG02293 | hp1 | a0001 | c0001 | t0001 | g0126 | AMR | PEL | VAMP7_chrX_155876345_155948769 | VAMP7 | chrX | 155876345 | 155948769 |
| HG02293 | hp2 | a0001 | c0001 | t0001 | g0009 | AMR | PEL | VAMP7_chrX_155876345_155948769 | VAMP7 | chrX | 155876345 | 155948769 |
| HG02300 | hp1 | a0001 | c0001 | t0002 | g0017 | AMR | PEL | VAMP7_chrX_155876345_155948769 | VAMP7 | chrX | 155876345 | 155948769 |
| HG02451 | hp1 | a0001 | c0001 | t0001 | g0047 | AFR | ACB | VAMP7_chrX_155876345_155948769 | VAMP7 | chrX | 155876345 | 155948769 |
| HG02451 | hp2 | a0001 | c0001 | t0001 | g0015 | AFR | ACB | VAMP7_chrX_155876345_155948769 | VAMP7 | chrX | 155876345 | 155948769 |
| HG02523 | hp1 | a0001 | c0001 | t0001 | g0120 | EAS | KHV | VAMP7_chrX_155876345_155948769 | VAMP7 | chrX | 155876345 | 155948769 |
| HG02523 | hp2 | a0001 | c0001 | t0001 | g0155 | EAS | KHV | VAMP7_chrX_155876345_155948769 | VAMP7 | chrX | 155876345 | 155948769 |
| HG02615 | hp1 | a0001 | c0001 | t0001 | g0123 | AFR | GWD | VAMP7_chrX_155876345_155948769 | VAMP7 | chrX | 155876345 | 155948769 |
| HG02615 | hp2 | a0001 | c0001 | t0001 | g0035 | AFR | GWD | VAMP7_chrX_155876345_155948769 | VAMP7 | chrX | 155876345 | 155948769 |
| HG02622 | hp1 | a0001 | c0001 | t0001 | g0029 | AFR | GWD | VAMP7_chrX_155876345_155948769 | VAMP7 | chrX | 155876345 | 155948769 |
| HG02622 | hp2 | a0001 | c0001 | t0001 | g0158 | AFR | GWD | VAMP7_chrX_155876345_155948769 | VAMP7 | chrX | 155876345 | 155948769 |
| HG02630 | hp1 | a0001 | c0001 | t0001 | g0033 | AFR | GWD | VAMP7_chrX_155876345_155948769 | VAMP7 | chrX | 155876345 | 155948769 |
| HG02630 | hp2 | a0001 | c0002 | t0001 | g0026 | AFR | GWD | VAMP7_chrX_155876345_155948769 | VAMP7 | chrX | 155876345 | 155948769 |
| HG02683 | hp1 | a0001 | c0001 | t0002 | g0138 | SAS | PJL | VAMP7_chrX_155876345_155948769 | VAMP7 | chrX | 155876345 | 155948769 |
| HG02683 | hp2 | a0001 | c0001 | t0001 | g0115 | SAS | PJL | VAMP7_chrX_155876345_155948769 | VAMP7 | chrX | 155876345 | 155948769 |
| HG02723 | hp1 | a0001 | c0001 | t0002 | g0003 | AFR | GWD | VAMP7_chrX_155876345_155948769 | VAMP7 | chrX | 155876345 | 155948769 |
| HG02723 | hp2 | a0001 | c0001 | t0001 | g0025 | AFR | GWD | VAMP7_chrX_155876345_155948769 | VAMP7 | chrX | 155876345 | 155948769 |
| HG02809 | hp1 | a0001 | c0001 | t0001 | g0015 | AFR | GWD | VAMP7_chrX_155876345_155948769 | VAMP7 | chrX | 155876345 | 155948769 |
| HG02809 | hp2 | a0001 | c0001 | t0001 | g0034 | AFR | GWD | VAMP7_chrX_155876345_155948769 | VAMP7 | chrX | 155876345 | 155948769 |
| HG02818 | hp1 | a0001 | c0001 | t0001 | g0061 | AFR | GWD | VAMP7_chrX_155876345_155948769 | VAMP7 | chrX | 155876345 | 155948769 |
| HG02818 | hp2 | a0001 | c0001 | t0003 | g0116 | AFR | GWD | VAMP7_chrX_155876345_155948769 | VAMP7 | chrX | 155876345 | 155948769 |
| HG02886 | hp1 | a0001 | c0001 | t0001 | g0122 | AFR | GWD | VAMP7_chrX_155876345_155948769 | VAMP7 | chrX | 155876345 | 155948769 |
| HG02886 | hp2 | a0001 | c0001 | t0001 | g0023 | AFR | GWD | VAMP7_chrX_155876345_155948769 | VAMP7 | chrX | 155876345 | 155948769 |
| HG02896 | hp1 | a0001 | c0001 | t0001 | g0040 | AFR | GWD | VAMP7_chrX_155876345_155948769 | VAMP7 | chrX | 155876345 | 155948769 |
| HG02896 | hp2 | a0001 | c0001 | t0001 | g0016 | AFR | GWD | VAMP7_chrX_155876345_155948769 | VAMP7 | chrX | 155876345 | 155948769 |
| HG02897 | hp1 | a0001 | c0001 | t0001 | g0075 | AFR | GWD | VAMP7_chrX_155876345_155948769 | VAMP7 | chrX | 155876345 | 155948769 |
| HG02897 | hp2 | a0001 | c0001 | t0001 | g0016 | AFR | GWD | VAMP7_chrX_155876345_155948769 | VAMP7 | chrX | 155876345 | 155948769 |
| HG02922 | hp1 | a0001 | c0001 | t0001 | g0014 | AFR | ESN | VAMP7_chrX_155876345_155948769 | VAMP7 | chrX | 155876345 | 155948769 |
| HG02922 | hp2 | a0001 | c0002 | t0001 | g0027 | AFR | ESN | VAMP7_chrX_155876345_155948769 | VAMP7 | chrX | 155876345 | 155948769 |
| HG02970 | hp1 | a0001 | c0002 | t0001 | g0028 | AFR | ESN | VAMP7_chrX_155876345_155948769 | VAMP7 | chrX | 155876345 | 155948769 |
| HG02970 | hp2 | a0001 | c0001 | t0001 | g0099 | AFR | ESN | VAMP7_chrX_155876345_155948769 | VAMP7 | chrX | 155876345 | 155948769 |
| HG02976 | hp1 | a0001 | c0001 | t0001 | g0002 | AFR | ESN | VAMP7_chrX_155876345_155948769 | VAMP7 | chrX | 155876345 | 155948769 |
| HG02976 | hp2 | a0001 | c0001 | t0001 | g0038 | AFR | ESN | VAMP7_chrX_155876345_155948769 | VAMP7 | chrX | 155876345 | 155948769 |
| HG03041 | hp1 | a0001 | c0001 | t0001 | g0157 | AFR | GWD | VAMP7_chrX_155876345_155948769 | VAMP7 | chrX | 155876345 | 155948769 |
| HG03041 | hp2 | a0001 | c0001 | t0001 | g0031 | AFR | GWD | VAMP7_chrX_155876345_155948769 | VAMP7 | chrX | 155876345 | 155948769 |
| HG03195 | hp1 | a0001 | c0001 | t0004 | g0020 | AFR | ESN | VAMP7_chrX_155876345_155948769 | VAMP7 | chrX | 155876345 | 155948769 |
| HG03195 | hp2 | a0001 | c0001 | t0001 | g0153 | AFR | ESN | VAMP7_chrX_155876345_155948769 | VAMP7 | chrX | 155876345 | 155948769 |
| HG03239 | hp1 | a0001 | c0001 | t0001 | g0058 | SAS | PJL | VAMP7_chrX_155876345_155948769 | VAMP7 | chrX | 155876345 | 155948769 |
| HG03239 | hp2 | a0001 | c0001 | t0001 | g0117 | SAS | PJL | VAMP7_chrX_155876345_155948769 | VAMP7 | chrX | 155876345 | 155948769 |
| HG03453 | hp1 | a0001 | c0001 | t0001 | g0030 | AFR | MSL | VAMP7_chrX_155876345_155948769 | VAMP7 | chrX | 155876345 | 155948769 |
| HG03453 | hp2 | a0001 | c0001 | t0001 | g0128 | AFR | MSL | VAMP7_chrX_155876345_155948769 | VAMP7 | chrX | 155876345 | 155948769 |
| HG03486 | hp1 | a0001 | c0001 | t0006 | g0018 | AFR | MSL | VAMP7_chrX_155876345_155948769 | VAMP7 | chrX | 155876345 | 155948769 |
| HG03486 | hp2 | a0001 | c0001 | t0001 | g0024 | AFR | MSL | VAMP7_chrX_155876345_155948769 | VAMP7 | chrX | 155876345 | 155948769 |
| HG03491 | hp1 | a0001 | c0001 | t0001 | g0143 | SAS | PJL | VAMP7_chrX_155876345_155948769 | VAMP7 | chrX | 155876345 | 155948769 |
| HG03491 | hp2 | a0001 | c0001 | t0001 | g0046 | SAS | PJL | VAMP7_chrX_155876345_155948769 | VAMP7 | chrX | 155876345 | 155948769 |
| HG03516 | hp1 | a0001 | c0001 | t0001 | g0127 | AFR | ESN | VAMP7_chrX_155876345_155948769 | VAMP7 | chrX | 155876345 | 155948769 |
| HG03516 | hp2 | a0001 | c0001 | t0001 | g0145 | AFR | ESN | VAMP7_chrX_155876345_155948769 | VAMP7 | chrX | 155876345 | 155948769 |
| HG03540 | hp1 | a0001 | c0001 | t0001 | g0076 | AFR | GWD | VAMP7_chrX_155876345_155948769 | VAMP7 | chrX | 155876345 | 155948769 |
| HG03540 | hp2 | a0001 | c0001 | t0001 | g0014 | AFR | GWD | VAMP7_chrX_155876345_155948769 | VAMP7 | chrX | 155876345 | 155948769 |
| HG03688 | hp1 | a0001 | c0001 | t0001 | g0053 | SAS | STU | VAMP7_chrX_155876345_155948769 | VAMP7 | chrX | 155876345 | 155948769 |
| HG04184 | hp1 | a0001 | c0001 | t0001 | g0032 | SAS | BEB | VAMP7_chrX_155876345_155948769 | VAMP7 | chrX | 155876345 | 155948769 |
| HG04184 | hp2 | a0001 | c0001 | t0001 | g0045 | SAS | BEB | VAMP7_chrX_155876345_155948769 | VAMP7 | chrX | 155876345 | 155948769 |
| HG04199 | hp1 | a0001 | c0001 | t0001 | g0051 | SAS | STU | VAMP7_chrX_155876345_155948769 | VAMP7 | chrX | 155876345 | 155948769 |
| NA18612 | hp2 | a0001 | c0001 | t0001 | g0150 | EAS | CHB | VAMP7_chrX_155876345_155948769 | VAMP7 | chrX | 155876345 | 155948769 |
| NA18747 | hp1 | a0001 | c0001 | t0001 | g0069 | EAS | CHB | VAMP7_chrX_155876345_155948769 | VAMP7 | chrX | 155876345 | 155948769 |
| NA18940 | hp1 | a0001 | c0001 | t0001 | g0083 | EAS | JPT | VAMP7_chrX_155876345_155948769 | VAMP7 | chrX | 155876345 | 155948769 |
| NA18941 | hp1 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | VAMP7_chrX_155876345_155948769 | VAMP7 | chrX | 155876345 | 155948769 |
| NA18941 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | VAMP7_chrX_155876345_155948769 | VAMP7 | chrX | 155876345 | 155948769 |
| NA18945 | hp1 | a0001 | c0001 | t0001 | g0064 | EAS | JPT | VAMP7_chrX_155876345_155948769 | VAMP7 | chrX | 155876345 | 155948769 |
| NA18953 | hp2 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | VAMP7_chrX_155876345_155948769 | VAMP7 | chrX | 155876345 | 155948769 |
| NA18954 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | VAMP7_chrX_155876345_155948769 | VAMP7 | chrX | 155876345 | 155948769 |
| NA18954 | hp2 | a0001 | c0001 | t0001 | g0129 | EAS | JPT | VAMP7_chrX_155876345_155948769 | VAMP7 | chrX | 155876345 | 155948769 |
| NA18959 | hp2 | a0001 | c0001 | t0001 | g0141 | EAS | JPT | VAMP7_chrX_155876345_155948769 | VAMP7 | chrX | 155876345 | 155948769 |
| NA18961 | hp1 | a0001 | c0001 | t0001 | g0113 | EAS | JPT | VAMP7_chrX_155876345_155948769 | VAMP7 | chrX | 155876345 | 155948769 |
| NA18965 | hp1 | a0001 | c0001 | t0005 | g0001 | EAS | JPT | VAMP7_chrX_155876345_155948769 | VAMP7 | chrX | 155876345 | 155948769 |
| NA18967 | hp1 | a0001 | c0001 | t0001 | g0087 | EAS | JPT | VAMP7_chrX_155876345_155948769 | VAMP7 | chrX | 155876345 | 155948769 |
| NA18968 | hp1 | a0001 | c0001 | t0001 | g0090 | EAS | JPT | VAMP7_chrX_155876345_155948769 | VAMP7 | chrX | 155876345 | 155948769 |
| NA18968 | hp2 | a0001 | c0001 | t0001 | g0109 | EAS | JPT | VAMP7_chrX_155876345_155948769 | VAMP7 | chrX | 155876345 | 155948769 |
| NA18971 | hp1 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | VAMP7_chrX_155876345_155948769 | VAMP7 | chrX | 155876345 | 155948769 |
| NA18974 | hp2 | a0001 | c0001 | t0002 | g0135 | EAS | JPT | VAMP7_chrX_155876345_155948769 | VAMP7 | chrX | 155876345 | 155948769 |
| NA18977 | hp1 | a0001 | c0001 | t0001 | g0068 | EAS | JPT | VAMP7_chrX_155876345_155948769 | VAMP7 | chrX | 155876345 | 155948769 |
| NA18980 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | VAMP7_chrX_155876345_155948769 | VAMP7 | chrX | 155876345 | 155948769 |
| NA18980 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | VAMP7_chrX_155876345_155948769 | VAMP7 | chrX | 155876345 | 155948769 |
| NA18981 | hp1 | a0001 | c0001 | t0001 | g0108 | EAS | JPT | VAMP7_chrX_155876345_155948769 | VAMP7 | chrX | 155876345 | 155948769 |
| NA18981 | hp2 | a0001 | c0001 | t0001 | g0048 | EAS | JPT | VAMP7_chrX_155876345_155948769 | VAMP7 | chrX | 155876345 | 155948769 |
| NA18985 | hp1 | a0001 | c0001 | t0001 | g0085 | EAS | JPT | VAMP7_chrX_155876345_155948769 | VAMP7 | chrX | 155876345 | 155948769 |
| NA18988 | hp1 | a0001 | c0001 | t0001 | g0124 | EAS | JPT | VAMP7_chrX_155876345_155948769 | VAMP7 | chrX | 155876345 | 155948769 |
| NA18989 | hp2 | a0001 | c0001 | t0001 | g0089 | EAS | JPT | VAMP7_chrX_155876345_155948769 | VAMP7 | chrX | 155876345 | 155948769 |
| NA18990 | hp1 | a0001 | c0001 | t0001 | g0094 | EAS | JPT | VAMP7_chrX_155876345_155948769 | VAMP7 | chrX | 155876345 | 155948769 |
| NA18992 | hp1 | a0001 | c0001 | t0001 | g0152 | EAS | JPT | VAMP7_chrX_155876345_155948769 | VAMP7 | chrX | 155876345 | 155948769 |
| NA18992 | hp2 | a0001 | c0001 | t0001 | g0082 | EAS | JPT | VAMP7_chrX_155876345_155948769 | VAMP7 | chrX | 155876345 | 155948769 |
| NA18994 | hp1 | a0001 | c0001 | t0001 | g0084 | EAS | JPT | VAMP7_chrX_155876345_155948769 | VAMP7 | chrX | 155876345 | 155948769 |
| NA18995 | hp1 | a0001 | c0001 | t0001 | g0072 | EAS | JPT | VAMP7_chrX_155876345_155948769 | VAMP7 | chrX | 155876345 | 155948769 |
| NA18998 | hp1 | a0001 | c0001 | t0001 | g0151 | EAS | JPT | VAMP7_chrX_155876345_155948769 | VAMP7 | chrX | 155876345 | 155948769 |
| NA18998 | hp2 | a0001 | c0001 | t0001 | g0088 | EAS | JPT | VAMP7_chrX_155876345_155948769 | VAMP7 | chrX | 155876345 | 155948769 |
| NA19001 | hp1 | a0001 | c0001 | t0001 | g0142 | EAS | JPT | VAMP7_chrX_155876345_155948769 | VAMP7 | chrX | 155876345 | 155948769 |
| NA19001 | hp2 | a0001 | c0001 | t0001 | g0147 | EAS | JPT | VAMP7_chrX_155876345_155948769 | VAMP7 | chrX | 155876345 | 155948769 |
| NA19005 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | VAMP7_chrX_155876345_155948769 | VAMP7 | chrX | 155876345 | 155948769 |
| NA19009 | hp2 | a0001 | c0001 | t0001 | g0081 | EAS | JPT | VAMP7_chrX_155876345_155948769 | VAMP7 | chrX | 155876345 | 155948769 |
| NA19010 | hp1 | a0001 | c0001 | t0001 | g0078 | EAS | JPT | VAMP7_chrX_155876345_155948769 | VAMP7 | chrX | 155876345 | 155948769 |
| NA19010 | hp2 | a0001 | c0001 | t0001 | g0097 | EAS | JPT | VAMP7_chrX_155876345_155948769 | VAMP7 | chrX | 155876345 | 155948769 |
| NA19011 | hp1 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | VAMP7_chrX_155876345_155948769 | VAMP7 | chrX | 155876345 | 155948769 |
| NA19011 | hp2 | a0001 | c0001 | t0001 | g0111 | EAS | JPT | VAMP7_chrX_155876345_155948769 | VAMP7 | chrX | 155876345 | 155948769 |
| NA19030 | hp1 | a0001 | c0001 | t0001 | g0077 | AFR | LWK | VAMP7_chrX_155876345_155948769 | VAMP7 | chrX | 155876345 | 155948769 |
| NA19030 | hp2 | a0001 | c0001 | t0001 | g0146 | AFR | LWK | VAMP7_chrX_155876345_155948769 | VAMP7 | chrX | 155876345 | 155948769 |
| NA19055 | hp1 | a0001 | c0001 | t0001 | g0096 | EAS | JPT | VAMP7_chrX_155876345_155948769 | VAMP7 | chrX | 155876345 | 155948769 |
| NA19057 | hp1 | a0001 | c0001 | t0001 | g0049 | EAS | JPT | VAMP7_chrX_155876345_155948769 | VAMP7 | chrX | 155876345 | 155948769 |
| NA19057 | hp2 | a0001 | c0001 | t0001 | g0105 | EAS | JPT | VAMP7_chrX_155876345_155948769 | VAMP7 | chrX | 155876345 | 155948769 |
| NA19060 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | VAMP7_chrX_155876345_155948769 | VAMP7 | chrX | 155876345 | 155948769 |
| NA19062 | hp1 | a0001 | c0001 | t0001 | g0063 | EAS | JPT | VAMP7_chrX_155876345_155948769 | VAMP7 | chrX | 155876345 | 155948769 |
| NA19067 | hp1 | a0001 | c0001 | t0001 | g0093 | EAS | JPT | VAMP7_chrX_155876345_155948769 | VAMP7 | chrX | 155876345 | 155948769 |
| NA19072 | hp1 | a0001 | c0001 | t0001 | g0065 | EAS | JPT | VAMP7_chrX_155876345_155948769 | VAMP7 | chrX | 155876345 | 155948769 |
| NA19075 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | VAMP7_chrX_155876345_155948769 | VAMP7 | chrX | 155876345 | 155948769 |
| NA19076 | hp1 | a0001 | c0001 | t0001 | g0066 | EAS | JPT | VAMP7_chrX_155876345_155948769 | VAMP7 | chrX | 155876345 | 155948769 |
| NA19079 | hp1 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | VAMP7_chrX_155876345_155948769 | VAMP7 | chrX | 155876345 | 155948769 |
| NA19080 | hp1 | a0001 | c0001 | t0001 | g0103 | EAS | JPT | VAMP7_chrX_155876345_155948769 | VAMP7 | chrX | 155876345 | 155948769 |
| NA19080 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | VAMP7_chrX_155876345_155948769 | VAMP7 | chrX | 155876345 | 155948769 |
| NA19085 | hp2 | a0001 | c0001 | t0001 | g0022 | EAS | JPT | VAMP7_chrX_155876345_155948769 | VAMP7 | chrX | 155876345 | 155948769 |
| NA19088 | hp1 | a0001 | c0001 | t0007 | g0091 | EAS | JPT | VAMP7_chrX_155876345_155948769 | VAMP7 | chrX | 155876345 | 155948769 |
| NA19089 | hp1 | a0001 | c0001 | t0001 | g0043 | EAS | JPT | VAMP7_chrX_155876345_155948769 | VAMP7 | chrX | 155876345 | 155948769 |
| NA19090 | hp1 | a0001 | c0001 | t0001 | g0149 | EAS | JPT | VAMP7_chrX_155876345_155948769 | VAMP7 | chrX | 155876345 | 155948769 |
| NA19090 | hp2 | a0001 | c0001 | t0001 | g0095 | EAS | JPT | VAMP7_chrX_155876345_155948769 | VAMP7 | chrX | 155876345 | 155948769 |
| NA19240 | hp1 | a0001 | c0001 | t0001 | g0002 | AFR | YRI | VAMP7_chrX_155876345_155948769 | VAMP7 | chrX | 155876345 | 155948769 |
| NA19240 | hp2 | a0001 | c0001 | t0001 | g0074 | AFR | YRI | VAMP7_chrX_155876345_155948769 | VAMP7 | chrX | 155876345 | 155948769 |
| NA20129 | hp1 | a0001 | c0001 | t0001 | g0080 | AFR | ASW | VAMP7_chrX_155876345_155948769 | VAMP7 | chrX | 155876345 | 155948769 |
| NA20129 | hp2 | a0001 | c0001 | t0001 | g0101 | AFR | ASW | VAMP7_chrX_155876345_155948769 | VAMP7 | chrX | 155876345 | 155948769 |
| HG01123 | hp1 | a0001 | c0001 | t0001 | g0106 | AMR | CLM | VAMP7_chrX_155876345_155948769 | VAMP7 | chrX | 155876345 | 155948769 |
| HG01123 | hp2 | a0001 | c0001 | t0001 | g0086 | AMR | CLM | VAMP7_chrX_155876345_155948769 | VAMP7 | chrX | 155876345 | 155948769 |
| HG02109 | hp1 | a0001 | c0001 | t0001 | g0002 | AFR | ACB | VAMP7_chrX_155876345_155948769 | VAMP7 | chrX | 155876345 | 155948769 |
| HG02109 | hp2 | a0001 | c0001 | t0001 | g0012 | AFR | ACB | VAMP7_chrX_155876345_155948769 | VAMP7 | chrX | 155876345 | 155948769 |
| HG02559 | hp1 | a0001 | c0001 | t0001 | g0054 | AFR | ACB | VAMP7_chrX_155876345_155948769 | VAMP7 | chrX | 155876345 | 155948769 |
| HG02559 | hp2 | a0001 | c0001 | t0001 | g0007 | AFR | ACB | VAMP7_chrX_155876345_155948769 | VAMP7 | chrX | 155876345 | 155948769 |
| HG03471 | hp1 | a0001 | c0001 | t0001 | g0012 | AFR | MSL | VAMP7_chrX_155876345_155948769 | VAMP7 | chrX | 155876345 | 155948769 |
| HG06807 | hp1 | a0001 | c0001 | t0001 | g0060 | AFR | USA | VAMP7_chrX_155876345_155948769 | VAMP7 | chrX | 155876345 | 155948769 |
| HG06807 | hp2 | a0001 | c0001 | t0001 | g0071 | AFR | USA | VAMP7_chrX_155876345_155948769 | VAMP7 | chrX | 155876345 | 155948769 |
| NA18955 | hp1 | a0001 | c0001 | t0001 | g0112 | EAS | JPT | VAMP7_chrX_155876345_155948769 | VAMP7 | chrX | 155876345 | 155948769 |
| homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0001 | g0050 | REF | REF | VAMP7_chrX_155876345_155948769 | VAMP7 | chrX | 155876345 | 155948769 |
| homoSapiens_grch38 | hp1 | a0001 | c0001 | t0001 | g0159 | REF | REF | VAMP7_chrX_155876345_155948769 | VAMP7 | chrX | 155876345 | 155948769 |
| chr:pos | ref | alt | # # of ahapid:amino-acid(protein) level |
ahapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|
| chr:pos | ref | alt | # # of chapid |
chapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chrX:155898234
|
C | G | 1 | a0001c0002 | 3 | HG02630.hp2 HG02922.hp2 HG02970.hp1 |
synonymous_variant | LOW | c.327C>G | p.Val109Val | VAMP7 | ENSG00000124333.16 | transcript | ENST00000286448.12 | protein_coding | 4/8 | 440/2594 | 327/663 | 109/220 | chrX | 155898234 |
| chr:pos | ref | alt | # # of thapid:transcript level |
thapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chrX:155881414
|
C | T | 1 | a0001c0001t0002 | 17 | HG00099.hp2 HG00639.hp1 HG01070.hp1 others(14): Show |
5_prime_UTR_variant | MODIFIER | c.-44C>T | VAMP7 | ENSG00000124333.16 | transcript | ENST00000286448.12 | protein_coding | 1/8 | 8053 | chrX | 155881414 | |||||
| chrX:155942459
|
C | T | 1 | a0001c0001t0007 | 1 | NA19088.hp1 | 3_prime_UTR_variant | MODIFIER | c.*508C>T | VAMP7 | ENSG00000124333.16 | transcript | ENST00000286448.12 | protein_coding | 8/8 | 508 | chrX | 155942459 | |||||
| chrX:155942681
|
A | G | 1 | a0001c0001t0006 | 1 | HG03486.hp1 | 3_prime_UTR_variant | MODIFIER | c.*730A>G | VAMP7 | ENSG00000124333.16 | transcript | ENST00000286448.12 | protein_coding | 8/8 | 730 | chrX | 155942681 | |||||
| chrX:155942801
|
A | G | 1 | a0001c0001t0005 | 1 | NA18965.hp1 | 3_prime_UTR_variant | MODIFIER | c.*850A>G | VAMP7 | ENSG00000124333.16 | transcript | ENST00000286448.12 | protein_coding | 8/8 | 850 | chrX | 155942801 | |||||
| chrX:155943179
|
C | T | 1 | a0001c0001t0004 | 1 | HG03195.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1228C>T | VAMP7 | ENSG00000124333.16 | transcript | ENST00000286448.12 | protein_coding | 8/8 | 1228 | chrX | 155943179 | |||||
| chrX:155943406
|
C | G | 1 | a0001c0001t0003 | 1 | HG02818.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1455C>G | VAMP7 | ENSG00000124333.16 | transcript | ENST00000286448.12 | protein_coding | 8/8 | 1455 | chrX | 155943406 | |||||
| chrX:155943707
|
A | G | 1 | a0001c0001t0006 | 1 | HG03486.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1756A>G | VAMP7 | ENSG00000124333.16 | transcript | ENST00000286448.12 | protein_coding | 8/8 | 1756 | chrX | 155943707 |
| chr:pos | ref | alt | # # of ghapid:genebody level |
ghapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | genebody_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chrX:155881467
|
G | GC | 159 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(156): Show | 183 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(180): Show |
intron_variant | MODIFIER | c.-10+21dupC | VAMP7 | ENSG00000124333.16 | transcript | ENST00000286448.12 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 155881467 | |||||
| chrX:155881674
|
A | G | 1 | a0001c0001t0001g0158 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.-10+226A>G | VAMP7 | ENSG00000124333.16 | transcript | ENST00000286448.12 | protein_coding | 1/7 | chrX | 155881674 | ||||||
| chrX:155881743
|
C | G | 4 | a0001c0001t0001g0154a0001c0001t0001g0155a0001c0001t0001g0156others(1): Show | 4 | HG01168.hp2 HG01517.hp1 HG02523.hp2 others(1): Show |
intron_variant | MODIFIER | c.-10+295C>G | VAMP7 | ENSG00000124333.16 | transcript | ENST00000286448.12 | protein_coding | 1/7 | chrX | 155881743 | ||||||
| chrX:155881872
|
C | T | 2 | a0001c0001t0001g0002a0001c0001t0001g0153 | 5 | HG02109.hp1 HG02280.hp1 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.-10+424C>T | VAMP7 | ENSG00000124333.16 | transcript | ENST00000286448.12 | protein_coding | 1/7 | chrX | 155881872 | ||||||
| chrX:155882039
|
G | C | 19 | a0001c0001t0001g0019a0001c0001t0001g0021a0001c0001t0001g0022others(16): Show | 19 | HG01070.hp2 HG02132.hp2 HG02615.hp2 others(16): Show |
intron_variant | MODIFIER | c.-10+591G>C | VAMP7 | ENSG00000124333.16 | transcript | ENST00000286448.12 | protein_coding | 1/7 | chrX | 155882039 | ||||||
| chrX:155882065
|
A | G | 1 | a0001c0001t0001g0158 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.-10+617A>G | VAMP7 | ENSG00000124333.16 | transcript | ENST00000286448.12 | protein_coding | 1/7 | chrX | 155882065 | ||||||
| chrX:155882066
|
A | G | 7 | a0001c0001t0001g0029a0001c0001t0001g0030a0001c0001t0001g0031others(4): Show | 7 | HG02615.hp2 HG02622.hp1 HG02630.hp1 others(4): Show |
intron_variant | MODIFIER | c.-10+618A>G | VAMP7 | ENSG00000124333.16 | transcript | ENST00000286448.12 | protein_coding | 1/7 | chrX | 155882066 | ||||||
| chrX:155882158
|
A | G | 6 | a0001c0001t0001g0147a0001c0001t0001g0148a0001c0001t0001g0149others(3): Show | 6 | HG00280.hp1 NA18612.hp2 NA18992.hp1 others(3): Show |
intron_variant | MODIFIER | c.-10+710A>G | VAMP7 | ENSG00000124333.16 | transcript | ENST00000286448.12 | protein_coding | 1/7 | chrX | 155882158 | ||||||
| chrX:155882171
|
G | A | 1 | a0001c0001t0006g0018 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.-10+723G>A | VAMP7 | ENSG00000124333.16 | transcript | ENST00000286448.12 | protein_coding | 1/7 | chrX | 155882171 | ||||||
| chrX:155882227
|
G | A | 1 | a0001c0001t0001g0158 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.-10+779G>A | VAMP7 | ENSG00000124333.16 | transcript | ENST00000286448.12 | protein_coding | 1/7 | chrX | 155882227 | ||||||
| chrX:155882301
|
C | G | 2 | a0001c0001t0001g0145a0001c0001t0001g0146 | 2 | HG03516.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.-10+853C>G | VAMP7 | ENSG00000124333.16 | transcript | ENST00000286448.12 | protein_coding | 1/7 | chrX | 155882301 | ||||||
| chrX:155882466
|
A | G | 3 | a0001c0002t0001g0026a0001c0002t0001g0027a0001c0002t0001g0028 | 3 | HG02630.hp2 HG02922.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.-10+1018A>G | VAMP7 | ENSG00000124333.16 | transcript | ENST00000286448.12 | protein_coding | 1/7 | chrX | 155882466 | ||||||
| chrX:155882522
|
CT | C | 1 | a0001c0001t0001g0019 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.-10+1075delT | VAMP7 | ENSG00000124333.16 | transcript | ENST00000286448.12 | protein_coding | 1/7 | chrX | 155882522 | ||||||
| chrX:155882647
|
A | G | 1 | a0001c0001t0001g0144 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.-10+1199A>G | VAMP7 | ENSG00000124333.16 | transcript | ENST00000286448.12 | protein_coding | 1/7 | chrX | 155882647 | ||||||
| chrX:155882656
|
T | G | 1 | a0001c0001t0001g0019 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.-10+1208T>G | VAMP7 | ENSG00000124333.16 | transcript | ENST00000286448.12 | protein_coding | 1/7 | chrX | 155882656 | ||||||
| chrX:155882883
|
G | A | 2 | a0001c0001t0002g0003a0001c0001t0002g0036 | 4 | HG01070.hp1 HG01071.hp2 HG01517.hp2 others(1): Show |
intron_variant | MODIFIER | c.-10+1435G>A | VAMP7 | ENSG00000124333.16 | transcript | ENST00000286448.12 | protein_coding | 1/7 | chrX | 155882883 | ||||||
| chrX:155883136
|
C | T | 1 | a0001c0001t0001g0143 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.-10+1688C>T | VAMP7 | ENSG00000124333.16 | transcript | ENST00000286448.12 | protein_coding | 1/7 | chrX | 155883136 | ||||||
| chrX:155883138
|
G | A | 3 | a0001c0001t0001g0007a0001c0001t0001g0037a0001c0001t0001g0038 | 4 | HG01884.hp1 HG02257.hp2 HG02559.hp2 others(1): Show |
intron_variant | MODIFIER | c.-10+1690G>A | VAMP7 | ENSG00000124333.16 | transcript | ENST00000286448.12 | protein_coding | 1/7 | chrX | 155883138 | ||||||
| chrX:155883578
|
G | A | 16 | a0001c0001t0001g0019a0001c0001t0001g0021a0001c0001t0001g0022others(13): Show | 16 | HG01070.hp2 HG02132.hp2 HG02615.hp2 others(13): Show |
intron_variant | MODIFIER | c.-10+2130G>A | VAMP7 | ENSG00000124333.16 | transcript | ENST00000286448.12 | protein_coding | 1/7 | chrX | 155883578 | ||||||
| chrX:155883579
|
A | T | 3 | a0001c0001t0001g0033a0001c0001t0001g0034a0001c0001t0001g0035 | 3 | HG02615.hp2 HG02630.hp1 HG02809.hp2 |
intron_variant | MODIFIER | c.-10+2131A>T | VAMP7 | ENSG00000124333.16 | transcript | ENST00000286448.12 | protein_coding | 1/7 | chrX | 155883579 | ||||||
| chrX:155883707
|
C | CT | 1 | a0001c0001t0001g0035 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.-10+2280dupT | VAMP7 | ENSG00000124333.16 | transcript | ENST00000286448.12 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 155883707 | |||||
| chrX:155883707
|
CT | C | 12 | a0001c0001t0001g0023a0001c0001t0001g0037a0001c0001t0001g0039others(9): Show | 12 | HG01081.hp2 HG01168.hp2 HG01169.hp2 others(9): Show |
intron_variant | MODIFIER | c.-10+2280delT | VAMP7 | ENSG00000124333.16 | transcript | ENST00000286448.12 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 155883707 | |||||
| chrX:155883707
|
CTT | C | 1 | a0001c0001t0001g0019 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.-10+2279_-10+2280d others(4): Show |
VAMP7 | ENSG00000124333.16 | transcript | ENST00000286448.12 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 155883707 | |||||
| chrX:155883857
|
C | T | 1 | a0001c0001t0001g0142 | 1 | NA19001.hp1 | intron_variant | MODIFIER | c.-10+2409C>T | VAMP7 | ENSG00000124333.16 | transcript | ENST00000286448.12 | protein_coding | 1/7 | chrX | 155883857 | ||||||
| chrX:155883877
|
A | AT | 1 | a0001c0001t0006g0018 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.-10+2438dupT | VAMP7 | ENSG00000124333.16 | transcript | ENST00000286448.12 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 155883877 | |||||
| chrX:155884169
|
C | G | 1 | a0001c0001t0001g0141 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.-10+2721C>G | VAMP7 | ENSG00000124333.16 | transcript | ENST00000286448.12 | protein_coding | 1/7 | chrX | 155884169 | ||||||
| chrX:155884240
|
G | A | 4 | a0001c0001t0001g0008a0001c0001t0001g0039a0001c0001t0001g0045others(1): Show | 5 | HG01081.hp2 HG01168.hp1 HG01169.hp1 others(2): Show |
intron_variant | MODIFIER | c.-10+2792G>A | VAMP7 | ENSG00000124333.16 | transcript | ENST00000286448.12 | protein_coding | 1/7 | chrX | 155884240 | ||||||
| chrX:155884277
|
G | A | 1 | a0001c0001t0001g0158 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.-10+2829G>A | VAMP7 | ENSG00000124333.16 | transcript | ENST00000286448.12 | protein_coding | 1/7 | chrX | 155884277 | ||||||
| chrX:155884317
|
G | C | 2 | a0001c0001t0001g0040a0001c0001t0001g0047 | 2 | HG02451.hp1 HG02896.hp1 |
intron_variant | MODIFIER | c.-10+2869G>C | VAMP7 | ENSG00000124333.16 | transcript | ENST00000286448.12 | protein_coding | 1/7 | chrX | 155884317 | ||||||
| chrX:155884374
|
G | A | 1 | a0001c0001t0006g0018 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.-10+2926G>A | VAMP7 | ENSG00000124333.16 | transcript | ENST00000286448.12 | protein_coding | 1/7 | chrX | 155884374 | ||||||
| chrX:155884550
|
C | G | 8 | a0001c0001t0001g0029a0001c0001t0001g0030a0001c0001t0001g0031others(5): Show | 8 | HG02615.hp2 HG02622.hp1 HG02630.hp1 others(5): Show |
intron_variant | MODIFIER | c.-10+3102C>G | VAMP7 | ENSG00000124333.16 | transcript | ENST00000286448.12 | protein_coding | 1/7 | chrX | 155884550 | ||||||
| chrX:155884592
|
C | G | 1 | a0001c0001t0001g0019 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.-10+3144C>G | VAMP7 | ENSG00000124333.16 | transcript | ENST00000286448.12 | protein_coding | 1/7 | chrX | 155884592 | ||||||
| chrX:155884752
|
T | C | 1 | a0001c0001t0001g0048 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.-10+3304T>C | VAMP7 | ENSG00000124333.16 | transcript | ENST00000286448.12 | protein_coding | 1/7 | chrX | 155884752 | ||||||
| chrX:155885099
|
A | G | 1 | a0001c0001t0001g0152 | 1 | NA18992.hp1 | intron_variant | MODIFIER | c.-10+3651A>G | VAMP7 | ENSG00000124333.16 | transcript | ENST00000286448.12 | protein_coding | 1/7 | chrX | 155885099 | ||||||
| chrX:155885320
|
C | G | 1 | a0001c0001t0001g0158 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.-10+3872C>G | VAMP7 | ENSG00000124333.16 | transcript | ENST00000286448.12 | protein_coding | 1/7 | chrX | 155885320 | ||||||
| chrX:155885524
|
C | T | 12 | a0001c0001t0002g0003a0001c0001t0002g0006a0001c0001t0002g0017others(9): Show | 17 | HG00099.hp2 HG00639.hp1 HG01070.hp1 others(14): Show |
intron_variant | MODIFIER | c.-9-3934C>T | VAMP7 | ENSG00000124333.16 | transcript | ENST00000286448.12 | protein_coding | 1/7 | chrX | 155885524 | ||||||
| chrX:155885582
|
A | G | 3 | a0001c0002t0001g0026a0001c0002t0001g0027a0001c0002t0001g0028 | 3 | HG02630.hp2 HG02922.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.-9-3876A>G | VAMP7 | ENSG00000124333.16 | transcript | ENST00000286448.12 | protein_coding | 1/7 | chrX | 155885582 | ||||||
| chrX:155886271
|
C | T | 1 | a0001c0001t0001g0157 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.-9-3187C>T | VAMP7 | ENSG00000124333.16 | transcript | ENST00000286448.12 | protein_coding | 1/7 | chrX | 155886271 | ||||||
| chrX:155886401
|
G | C | 1 | a0001c0001t0001g0049 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.-9-3057G>C | VAMP7 | ENSG00000124333.16 | transcript | ENST00000286448.12 | protein_coding | 1/7 | chrX | 155886401 | ||||||
| chrX:155886500
|
T | C | 1 | a0001c0001t0001g0050 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.-9-2958T>C | VAMP7 | ENSG00000124333.16 | transcript | ENST00000286448.12 | protein_coding | 1/7 | chrX | 155886500 | ||||||
| chrX:155886904
|
CA | C | 159 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(156): Show | 183 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(180): Show |
intron_variant | MODIFIER | c.-9-2552delA | VAMP7 | ENSG00000124333.16 | transcript | ENST00000286448.12 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 155886904 | |||||
| chrX:155886911
|
C | T | 159 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(156): Show | 183 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(180): Show |
intron_variant | MODIFIER | c.-9-2547C>T | VAMP7 | ENSG00000124333.16 | transcript | ENST00000286448.12 | protein_coding | 1/7 | chrX | 155886911 | ||||||
| chrX:155886915
|
C | CT | 159 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(156): Show | 183 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(180): Show |
intron_variant | MODIFIER | c.-9-2542dupT | VAMP7 | ENSG00000124333.16 | transcript | ENST00000286448.12 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 155886915 | |||||
| chrX:155886936
|
GGCT | G | 17 | a0001c0001t0001g0019a0001c0001t0001g0021a0001c0001t0001g0022others(14): Show | 17 | HG01070.hp2 HG02132.hp2 HG02615.hp2 others(14): Show |
intron_variant | MODIFIER | c.-9-2515_-9-2513del others(3): Show |
VAMP7 | ENSG00000124333.16 | transcript | ENST00000286448.12 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 155886936 | |||||
| chrX:155886969
|
G | T | 3 | a0001c0001t0001g0130a0001c0001t0001g0131a0001c0001t0001g0132 | 3 | HG00558.hp2 HG01361.hp2 HG01993.hp2 |
intron_variant | MODIFIER | c.-9-2489G>T | VAMP7 | ENSG00000124333.16 | transcript | ENST00000286448.12 | protein_coding | 1/7 | chrX | 155886969 | ||||||
| chrX:155887018
|
C | G | 1 | a0001c0001t0002g0140 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.-9-2440C>G | VAMP7 | ENSG00000124333.16 | transcript | ENST00000286448.12 | protein_coding | 1/7 | chrX | 155887018 | ||||||
| chrX:155887059
|
G | C | 1 | a0001c0001t0001g0019 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.-9-2399G>C | VAMP7 | ENSG00000124333.16 | transcript | ENST00000286448.12 | protein_coding | 1/7 | chrX | 155887059 | ||||||
| chrX:155887111
|
C | T | 1 | a0001c0001t0001g0019 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.-9-2347C>T | VAMP7 | ENSG00000124333.16 | transcript | ENST00000286448.12 | protein_coding | 1/7 | chrX | 155887111 | ||||||
| chrX:155887231
|
AT | A | 1 | a0001c0001t0001g0023 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.-9-2217delT | VAMP7 | ENSG00000124333.16 | transcript | ENST00000286448.12 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 155887231 | |||||
| chrX:155887348
|
C | T | 3 | a0001c0002t0001g0026a0001c0002t0001g0027a0001c0002t0001g0028 | 3 | HG02630.hp2 HG02922.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.-9-2110C>T | VAMP7 | ENSG00000124333.16 | transcript | ENST00000286448.12 | protein_coding | 1/7 | chrX | 155887348 | ||||||
| chrX:155887400
|
G | C | 1 | a0001c0001t0001g0157 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.-9-2058G>C | VAMP7 | ENSG00000124333.16 | transcript | ENST00000286448.12 | protein_coding | 1/7 | chrX | 155887400 | ||||||
| chrX:155887519
|
T | C | 7 | a0001c0001t0001g0029a0001c0001t0001g0030a0001c0001t0001g0031others(4): Show | 7 | HG02615.hp2 HG02622.hp1 HG02630.hp1 others(4): Show |
intron_variant | MODIFIER | c.-9-1939T>C | VAMP7 | ENSG00000124333.16 | transcript | ENST00000286448.12 | protein_coding | 1/7 | chrX | 155887519 | ||||||
| chrX:155887637
|
A | G | 1 | a0001c0001t0006g0018 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.-9-1821A>G | VAMP7 | ENSG00000124333.16 | transcript | ENST00000286448.12 | protein_coding | 1/7 | chrX | 155887637 | ||||||
| chrX:155887666
|
T | C | 19 | a0001c0001t0001g0019a0001c0001t0001g0021a0001c0001t0001g0022others(16): Show | 19 | HG01070.hp2 HG02132.hp2 HG02615.hp2 others(16): Show |
intron_variant | MODIFIER | c.-9-1792T>C | VAMP7 | ENSG00000124333.16 | transcript | ENST00000286448.12 | protein_coding | 1/7 | chrX | 155887666 | ||||||
| chrX:155887718
|
C | T | 1 | a0001c0001t0001g0129 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.-9-1740C>T | VAMP7 | ENSG00000124333.16 | transcript | ENST00000286448.12 | protein_coding | 1/7 | chrX | 155887718 | ||||||
| chrX:155887756
|
C | T | 5 | a0001c0001t0001g0014a0001c0001t0001g0015a0001c0001t0001g0016others(2): Show | 8 | HG02451.hp2 HG02809.hp1 HG02896.hp2 others(5): Show |
intron_variant | MODIFIER | c.-9-1702C>T | VAMP7 | ENSG00000124333.16 | transcript | ENST00000286448.12 | protein_coding | 1/7 | chrX | 155887756 | ||||||
| chrX:155887765
|
CA | C | 7 | a0001c0001t0001g0021a0001c0001t0001g0022a0001c0001t0001g0023others(4): Show | 7 | HG02132.hp2 HG02622.hp2 HG02630.hp2 others(4): Show |
intron_variant | MODIFIER | c.-9-1684delA | VAMP7 | ENSG00000124333.16 | transcript | ENST00000286448.12 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 155887765 | |||||
| chrX:155887798
|
G | A | 2 | a0001c0001t0001g0023a0001c0001t0001g0158 | 2 | HG02622.hp2 HG02886.hp2 |
intron_variant | MODIFIER | c.-9-1660G>A | VAMP7 | ENSG00000124333.16 | transcript | ENST00000286448.12 | protein_coding | 1/7 | chrX | 155887798 | ||||||
| chrX:155887810
|
A | G | 2 | a0001c0001t0001g0145a0001c0001t0001g0146 | 2 | HG03516.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.-9-1648A>G | VAMP7 | ENSG00000124333.16 | transcript | ENST00000286448.12 | protein_coding | 1/7 | chrX | 155887810 | ||||||
| chrX:155887937
|
C | CA | 17 | a0001c0001t0001g0024a0001c0001t0001g0025a0001c0001t0001g0039others(14): Show | 17 | HG00639.hp2 HG00741.hp1 HG01071.hp1 others(14): Show |
intron_variant | MODIFIER | c.-9-1505dupA | VAMP7 | ENSG00000124333.16 | transcript | ENST00000286448.12 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 155887937 | |||||
| chrX:155887937
|
C | CAA | 2 | a0001c0001t0001g0019a0001c0001t0006g0018 | 2 | HG01070.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.-9-1506_-9-1505dup others(2): Show |
VAMP7 | ENSG00000124333.16 | transcript | ENST00000286448.12 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 155887937 | |||||
| chrX:155888030
|
TG | T | 6 | a0001c0001t0001g0021a0001c0001t0001g0022a0001c0001t0006g0018others(3): Show | 6 | HG02132.hp2 HG02630.hp2 HG02922.hp2 others(3): Show |
intron_variant | MODIFIER | c.-9-1426delG | VAMP7 | ENSG00000124333.16 | transcript | ENST00000286448.12 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 155888030 | |||||
| chrX:155888109
|
T | C | 1 | a0001c0001t0006g0018 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.-9-1349T>C | VAMP7 | ENSG00000124333.16 | transcript | ENST00000286448.12 | protein_coding | 1/7 | chrX | 155888109 | ||||||
| chrX:155888274
|
C | T | 1 | a0001c0001t0001g0019 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.-9-1184C>T | VAMP7 | ENSG00000124333.16 | transcript | ENST00000286448.12 | protein_coding | 1/7 | chrX | 155888274 | ||||||
| chrX:155888280
|
ATGTT | A | 1 | a0001c0001t0001g0019 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.-9-1174_-9-1171del others(4): Show |
VAMP7 | ENSG00000124333.16 | transcript | ENST00000286448.12 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 155888280 | |||||
| chrX:155888299
|
G | T | 1 | a0001c0001t0001g0158 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.-9-1159G>T | VAMP7 | ENSG00000124333.16 | transcript | ENST00000286448.12 | protein_coding | 1/7 | chrX | 155888299 | ||||||
| chrX:155888354
|
G | A | 1 | a0001c0001t0001g0158 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.-9-1104G>A | VAMP7 | ENSG00000124333.16 | transcript | ENST00000286448.12 | protein_coding | 1/7 | chrX | 155888354 | ||||||
| chrX:155888556
|
G | T | 1 | a0001c0001t0001g0126 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.-9-902G>T | VAMP7 | ENSG00000124333.16 | transcript | ENST00000286448.12 | protein_coding | 1/7 | chrX | 155888556 | ||||||
| chrX:155888683
|
T | G | 1 | a0001c0001t0001g0019 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.-9-775T>G | VAMP7 | ENSG00000124333.16 | transcript | ENST00000286448.12 | protein_coding | 1/7 | chrX | 155888683 | ||||||
| chrX:155888746
|
C | G | 1 | a0001c0001t0001g0125 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.-9-712C>G | VAMP7 | ENSG00000124333.16 | transcript | ENST00000286448.12 | protein_coding | 1/7 | chrX | 155888746 | ||||||
| chrX:155888999
|
A | G | 2 | a0001c0001t0001g0021a0001c0001t0001g0022 | 2 | HG02132.hp2 NA19085.hp2 |
intron_variant | MODIFIER | c.-9-459A>G | VAMP7 | ENSG00000124333.16 | transcript | ENST00000286448.12 | protein_coding | 1/7 | chrX | 155888999 | ||||||
| chrX:155889159
|
G | A | 1 | a0001c0001t0001g0023 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.-9-299G>A | VAMP7 | ENSG00000124333.16 | transcript | ENST00000286448.12 | protein_coding | 1/7 | chrX | 155889159 | ||||||
| chrX:155889362
|
T | C | 2 | a0001c0001t0001g0024a0001c0001t0001g0025 | 2 | HG02723.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.-9-96T>C | VAMP7 | ENSG00000124333.16 | transcript | ENST00000286448.12 | protein_coding | 1/7 | chrX | 155889362 | ||||||
| chrX:155889816
|
G | T | 4 | a0001c0001t0001g0008a0001c0001t0001g0039a0001c0001t0001g0045others(1): Show | 5 | HG01081.hp2 HG01168.hp1 HG01169.hp1 others(2): Show |
intron_variant | MODIFIER | c.146+204G>T | VAMP7 | ENSG00000124333.16 | transcript | ENST00000286448.12 | protein_coding | 2/7 | chrX | 155889816 | ||||||
| chrX:155889825
|
T | G | 1 | a0001c0001t0001g0158 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.146+213T>G | VAMP7 | ENSG00000124333.16 | transcript | ENST00000286448.12 | protein_coding | 2/7 | chrX | 155889825 | ||||||
| chrX:155889838
|
T | TG | 159 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(156): Show | 183 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(180): Show |
intron_variant | MODIFIER | c.146+227dupG | VAMP7 | ENSG00000124333.16 | transcript | ENST00000286448.12 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chrX | 155889838 | |||||
| chrX:155889887
|
GA | G | 159 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(156): Show | 183 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(180): Show |
intron_variant | MODIFIER | c.146+279delA | VAMP7 | ENSG00000124333.16 | transcript | ENST00000286448.12 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chrX | 155889887 | |||||
| chrX:155889918
|
CT | C | 5 | a0001c0001t0001g0021a0001c0001t0001g0022a0001c0002t0001g0026others(2): Show | 5 | HG02132.hp2 HG02630.hp2 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.146+309delT | VAMP7 | ENSG00000124333.16 | transcript | ENST00000286448.12 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chrX | 155889918 | |||||
| chrX:155889941
|
A | T | 4 | a0001c0001t0001g0044a0001c0001t0001g0058a0001c0001t0001g0059others(1): Show | 4 | HG00741.hp1 HG01169.hp2 HG01346.hp1 others(1): Show |
intron_variant | MODIFIER | c.146+329A>T | VAMP7 | ENSG00000124333.16 | transcript | ENST00000286448.12 | protein_coding | 2/7 | chrX | 155889941 | ||||||
| chrX:155889985
|
G | C | 92 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(89): Show | 110 | HG00099.hp2 HG00408.hp1 HG00558.hp2 others(107): Show |
intron_variant | MODIFIER | c.146+373G>C | VAMP7 | ENSG00000124333.16 | transcript | ENST00000286448.12 | protein_coding | 2/7 | chrX | 155889985 | ||||||
| chrX:155890005
|
G | A | 2 | a0001c0001t0001g0158a0001c0001t0006g0018 | 2 | HG02622.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.146+393G>A | VAMP7 | ENSG00000124333.16 | transcript | ENST00000286448.12 | protein_coding | 2/7 | chrX | 155890005 | ||||||
| chrX:155890149
|
G | T | 1 | a0001c0001t0001g0057 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.146+537G>T | VAMP7 | ENSG00000124333.16 | transcript | ENST00000286448.12 | protein_coding | 2/7 | chrX | 155890149 | ||||||
| chrX:155890350
|
T | TTTTA | 11 | a0001c0001t0001g0002a0001c0001t0001g0021a0001c0001t0001g0022others(8): Show | 14 | HG02109.hp1 HG02132.hp2 HG02257.hp1 others(11): Show |
intron_variant | MODIFIER | c.146+763_146+766dup others(4): Show |
VAMP7 | ENSG00000124333.16 | transcript | ENST00000286448.12 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chrX | 155890350 | |||||
| chrX:155890412
|
G | A | 17 | a0001c0001t0001g0005a0001c0001t0001g0103a0001c0001t0001g0104others(14): Show | 19 | HG00280.hp1 HG00558.hp1 HG01123.hp1 others(16): Show |
intron_variant | MODIFIER | c.146+800G>A | VAMP7 | ENSG00000124333.16 | transcript | ENST00000286448.12 | protein_coding | 2/7 | chrX | 155890412 | ||||||
| chrX:155890470
|
C | T | 1 | a0001c0001t0001g0098 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.146+858C>T | VAMP7 | ENSG00000124333.16 | transcript | ENST00000286448.12 | protein_coding | 2/7 | chrX | 155890470 | ||||||
| chrX:155890580
|
C | G | 1 | a0001c0001t0001g0050 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.146+968C>G | VAMP7 | ENSG00000124333.16 | transcript | ENST00000286448.12 | protein_coding | 2/7 | chrX | 155890580 | ||||||
| chrX:155890602
|
TC | T | 15 | a0001c0001t0001g0001a0001c0001t0001g0043a0001c0001t0001g0087others(12): Show | 17 | HG00408.hp1 NA18941.hp2 NA18954.hp2 others(14): Show |
intron_variant | MODIFIER | c.146+991delC | VAMP7 | ENSG00000124333.16 | transcript | ENST00000286448.12 | protein_coding | 2/7 | chrX | 155890602 | ||||||
| chrX:155890825
|
A | G | 1 | a0001c0001t0001g0158 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.146+1213A>G | VAMP7 | ENSG00000124333.16 | transcript | ENST00000286448.12 | protein_coding | 2/7 | chrX | 155890825 | ||||||
| chrX:155890883
|
T | C | 1 | a0001c0001t0004g0020 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.146+1271T>C | VAMP7 | ENSG00000124333.16 | transcript | ENST00000286448.12 | protein_coding | 2/7 | chrX | 155890883 | ||||||
| chrX:155890969
|
C | T | 1 | a0001c0001t0004g0020 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.146+1357C>T | VAMP7 | ENSG00000124333.16 | transcript | ENST00000286448.12 | protein_coding | 2/7 | chrX | 155890969 | ||||||
| chrX:155891017
|
CT | C | 1 | a0001c0001t0001g0041 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.146+1407delT | VAMP7 | ENSG00000124333.16 | transcript | ENST00000286448.12 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chrX | 155891017 | |||||
| chrX:155891146
|
A | C | 1 | a0001c0001t0001g0158 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.146+1534A>C | VAMP7 | ENSG00000124333.16 | transcript | ENST00000286448.12 | protein_coding | 2/7 | chrX | 155891146 | ||||||
| chrX:155891269
|
A | T | 1 | a0001c0001t0001g0111 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.146+1657A>T | VAMP7 | ENSG00000124333.16 | transcript | ENST00000286448.12 | protein_coding | 2/7 | chrX | 155891269 | ||||||
| chrX:155891287
|
C | T | 101 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(98): Show | 119 | HG00099.hp2 HG00408.hp1 HG00558.hp2 others(116): Show |
intron_variant | MODIFIER | c.146+1675C>T | VAMP7 | ENSG00000124333.16 | transcript | ENST00000286448.12 | protein_coding | 2/7 | chrX | 155891287 | ||||||
| chrX:155891389
|
G | T | 4 | a0001c0001t0001g0008a0001c0001t0001g0039a0001c0001t0001g0045others(1): Show | 5 | HG01081.hp2 HG01168.hp1 HG01169.hp1 others(2): Show |
intron_variant | MODIFIER | c.146+1777G>T | VAMP7 | ENSG00000124333.16 | transcript | ENST00000286448.12 | protein_coding | 2/7 | chrX | 155891389 | ||||||
| chrX:155891793
|
A | G | 2 | a0001c0001t0001g0096a0001c0001t0001g0097 | 2 | NA19010.hp2 NA19055.hp1 |
intron_variant | MODIFIER | c.146+2181A>G | VAMP7 | ENSG00000124333.16 | transcript | ENST00000286448.12 | protein_coding | 2/7 | chrX | 155891793 | ||||||
| chrX:155891842
|
G | A | 3 | a0001c0001t0001g0087a0001c0001t0001g0088a0001c0001t0001g0089 | 3 | NA18967.hp1 NA18989.hp2 NA18998.hp2 |
intron_variant | MODIFIER | c.146+2230G>A | VAMP7 | ENSG00000124333.16 | transcript | ENST00000286448.12 | protein_coding | 2/7 | chrX | 155891842 | ||||||
| chrX:155891863
|
T | A | 96 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(93): Show | 114 | HG00099.hp2 HG00408.hp1 HG00558.hp2 others(111): Show |
intron_variant | MODIFIER | c.146+2251T>A | VAMP7 | ENSG00000124333.16 | transcript | ENST00000286448.12 | protein_coding | 2/7 | chrX | 155891863 | ||||||
| chrX:155891877
|
A | G | 1 | a0001c0001t0001g0023 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.146+2265A>G | VAMP7 | ENSG00000124333.16 | transcript | ENST00000286448.12 | protein_coding | 2/7 | chrX | 155891877 | ||||||
| chrX:155891900
|
C | T | 1 | a0001c0001t0001g0008 | 2 | HG01168.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.146+2288C>T | VAMP7 | ENSG00000124333.16 | transcript | ENST00000286448.12 | protein_coding | 2/7 | chrX | 155891900 | ||||||
| chrX:155892163
|
G | T | 2 | a0001c0001t0001g0002a0001c0001t0001g0153 | 5 | HG02109.hp1 HG02280.hp1 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.146+2551G>T | VAMP7 | ENSG00000124333.16 | transcript | ENST00000286448.12 | protein_coding | 2/7 | chrX | 155892163 | ||||||
| chrX:155892213
|
G | T | 1 | a0001c0001t0001g0019 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.146+2601G>T | VAMP7 | ENSG00000124333.16 | transcript | ENST00000286448.12 | protein_coding | 2/7 | chrX | 155892213 | ||||||
| chrX:155892279
|
C | T | 3 | a0001c0002t0001g0026a0001c0002t0001g0027a0001c0002t0001g0028 | 3 | HG02630.hp2 HG02922.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.146+2667C>T | VAMP7 | ENSG00000124333.16 | transcript | ENST00000286448.12 | protein_coding | 2/7 | chrX | 155892279 | ||||||
| chrX:155892385
|
A | G | 1 | a0001c0001t0001g0086 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.146+2773A>G | VAMP7 | ENSG00000124333.16 | transcript | ENST00000286448.12 | protein_coding | 2/7 | chrX | 155892385 | ||||||
| chrX:155892424
|
A | C | 5 | a0001c0001t0002g0003a0001c0001t0002g0017a0001c0001t0002g0036others(2): Show | 8 | HG00099.hp2 HG01070.hp1 HG01071.hp2 others(5): Show |
intron_variant | MODIFIER | c.146+2812A>C | VAMP7 | ENSG00000124333.16 | transcript | ENST00000286448.12 | protein_coding | 2/7 | chrX | 155892424 | ||||||
| chrX:155892647
|
G | T | 4 | a0001c0001t0001g0099a0001c0001t0001g0100a0001c0001t0001g0101others(1): Show | 4 | HG02257.hp1 HG02280.hp2 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.147-2976G>T | VAMP7 | ENSG00000124333.16 | transcript | ENST00000286448.12 | protein_coding | 2/7 | chrX | 155892647 | ||||||
| chrX:155892733
|
T | C | 1 | a0001c0001t0001g0158 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.147-2890T>C | VAMP7 | ENSG00000124333.16 | transcript | ENST00000286448.12 | protein_coding | 2/7 | chrX | 155892733 | ||||||
| chrX:155892741
|
G | GTAT | 98 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(95): Show | 116 | HG00099.hp2 HG00408.hp1 HG00558.hp2 others(113): Show |
intron_variant | MODIFIER | c.147-2856_147-2854d others(5): Show |
VAMP7 | ENSG00000124333.16 | transcript | ENST00000286448.12 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chrX | 155892741 | |||||
| chrX:155892741
|
G | GTATTAT | 6 | a0001c0001t0001g0024a0001c0001t0001g0033a0001c0001t0001g0034others(3): Show | 6 | HG02615.hp2 HG02630.hp1 HG02809.hp2 others(3): Show |
intron_variant | MODIFIER | c.147-2859_147-2854d others(8): Show |
VAMP7 | ENSG00000124333.16 | transcript | ENST00000286448.12 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chrX | 155892741 | |||||
| chrX:155892741
|
G | GTATTATT others(2): Show |
1 | a0001c0001t0001g0031 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.147-2862_147-2854d others(11): Show |
VAMP7 | ENSG00000124333.16 | transcript | ENST00000286448.12 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chrX | 155892741 | |||||
| chrX:155892741
|
G | GTATTATT others(5): Show |
1 | a0001c0001t0001g0030 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.147-2865_147-2854d others(14): Show |
VAMP7 | ENSG00000124333.16 | transcript | ENST00000286448.12 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chrX | 155892741 | |||||
| chrX:155892741
|
GTAT | G | 1 | a0001c0001t0001g0023 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.147-2856_147-2854d others(5): Show |
VAMP7 | ENSG00000124333.16 | transcript | ENST00000286448.12 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chrX | 155892741 | |||||
| chrX:155892774
|
C | T | 3 | a0001c0001t0001g0007a0001c0001t0001g0037a0001c0001t0001g0038 | 4 | HG01884.hp1 HG02257.hp2 HG02559.hp2 others(1): Show |
intron_variant | MODIFIER | c.147-2849C>T | VAMP7 | ENSG00000124333.16 | transcript | ENST00000286448.12 | protein_coding | 2/7 | chrX | 155892774 | ||||||
| chrX:155892783
|
G | C | 5 | a0001c0001t0001g0030a0001c0001t0001g0031a0001c0001t0001g0033others(2): Show | 5 | HG02615.hp2 HG02630.hp1 HG02809.hp2 others(2): Show |
intron_variant | MODIFIER | c.147-2840G>C | VAMP7 | ENSG00000124333.16 | transcript | ENST00000286448.12 | protein_coding | 2/7 | chrX | 155892783 | ||||||
| chrX:155892784
|
C | T | 1 | a0001c0001t0006g0018 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.147-2839C>T | VAMP7 | ENSG00000124333.16 | transcript | ENST00000286448.12 | protein_coding | 2/7 | chrX | 155892784 | ||||||
| chrX:155892906
|
C | T | 1 | a0001c0001t0001g0156 | 1 | HG01517.hp1 | intron_variant | MODIFIER | c.147-2717C>T | VAMP7 | ENSG00000124333.16 | transcript | ENST00000286448.12 | protein_coding | 2/7 | chrX | 155892906 | ||||||
| chrX:155893120
|
G | A | 4 | a0001c0001t0001g0002a0001c0001t0001g0060a0001c0001t0001g0062others(1): Show | 7 | HG01891.hp1 HG02109.hp1 HG02280.hp1 others(4): Show |
intron_variant | MODIFIER | c.147-2503G>A | VAMP7 | ENSG00000124333.16 | transcript | ENST00000286448.12 | protein_coding | 2/7 | chrX | 155893120 | ||||||
| chrX:155893180
|
GA | G | 1 | a0001c0001t0001g0060 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.147-2442delA | VAMP7 | ENSG00000124333.16 | transcript | ENST00000286448.12 | protein_coding | 2/7 | chrX | 155893180 | ||||||
| chrX:155893301
|
A | G | 2 | a0001c0001t0001g0023a0001c0001t0006g0018 | 2 | HG02886.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.147-2322A>G | VAMP7 | ENSG00000124333.16 | transcript | ENST00000286448.12 | protein_coding | 2/7 | chrX | 155893301 | ||||||
| chrX:155893375
|
T | C | 1 | a0001c0001t0001g0023 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.147-2248T>C | VAMP7 | ENSG00000124333.16 | transcript | ENST00000286448.12 | protein_coding | 2/7 | chrX | 155893375 | ||||||
| chrX:155893399
|
GAGTA | G | 2 | a0001c0001t0001g0023a0001c0001t0006g0018 | 2 | HG02886.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.147-2216_147-2213d others(6): Show |
VAMP7 | ENSG00000124333.16 | transcript | ENST00000286448.12 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chrX | 155893399 | |||||
| chrX:155893574
|
C | T | 91 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(88): Show | 109 | HG00099.hp2 HG00408.hp1 HG00558.hp2 others(106): Show |
intron_variant | MODIFIER | c.147-2049C>T | VAMP7 | ENSG00000124333.16 | transcript | ENST00000286448.12 | protein_coding | 2/7 | chrX | 155893574 | ||||||
| chrX:155893777
|
T | C | 1 | a0001c0001t0001g0147 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.147-1846T>C | VAMP7 | ENSG00000124333.16 | transcript | ENST00000286448.12 | protein_coding | 2/7 | chrX | 155893777 | ||||||
| chrX:155893899
|
C | T | 1 | a0001c0001t0001g0019 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.147-1724C>T | VAMP7 | ENSG00000124333.16 | transcript | ENST00000286448.12 | protein_coding | 2/7 | chrX | 155893899 | ||||||
| chrX:155894005
|
G | T | 90 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(87): Show | 108 | HG00099.hp2 HG00408.hp1 HG00558.hp2 others(105): Show |
intron_variant | MODIFIER | c.147-1618G>T | VAMP7 | ENSG00000124333.16 | transcript | ENST00000286448.12 | protein_coding | 2/7 | chrX | 155894005 | ||||||
| chrX:155894065
|
C | T | 1 | a0001c0001t0006g0018 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.147-1558C>T | VAMP7 | ENSG00000124333.16 | transcript | ENST00000286448.12 | protein_coding | 2/7 | chrX | 155894065 | ||||||
| chrX:155894301
|
G | GT | 19 | a0001c0001t0001g0001a0001c0001t0001g0043a0001c0001t0001g0081others(16): Show | 21 | HG00408.hp1 HG02148.hp1 NA18940.hp1 others(18): Show |
intron_variant | MODIFIER | c.147-1300dupT | VAMP7 | ENSG00000124333.16 | transcript | ENST00000286448.12 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chrX | 155894301 | |||||
| chrX:155894301
|
G | GTT | 1 | a0001c0001t0001g0095 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.147-1301_147-1300d others(4): Show |
VAMP7 | ENSG00000124333.16 | transcript | ENST00000286448.12 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chrX | 155894301 | |||||
| chrX:155894301
|
G | GTTT | 4 | a0001c0001t0001g0019a0001c0001t0001g0033a0001c0001t0001g0034others(1): Show | 4 | HG01070.hp2 HG02615.hp2 HG02630.hp1 others(1): Show |
intron_variant | MODIFIER | c.147-1302_147-1300d others(5): Show |
VAMP7 | ENSG00000124333.16 | transcript | ENST00000286448.12 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chrX | 155894301 | |||||
| chrX:155894301
|
GT | G | 4 | a0001c0001t0001g0063a0001c0001t0001g0154a0001c0001t0002g0036others(1): Show | 4 | HG01070.hp1 HG01168.hp2 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.147-1300delT | VAMP7 | ENSG00000124333.16 | transcript | ENST00000286448.12 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chrX | 155894301 | |||||
| chrX:155894307
|
T | TG | 1 | a0001c0001t0001g0096 | 1 | NA19055.hp1 | intron_variant | MODIFIER | c.147-1316_147-1315i others(3): Show |
VAMP7 | ENSG00000124333.16 | transcript | ENST00000286448.12 | protein_coding | 2/7 | chrX | 155894307 | ||||||
| chrX:155894313
|
T | TG | 3 | a0001c0001t0001g0024a0001c0001t0001g0025a0001c0001t0004g0020 | 3 | HG02723.hp2 HG03195.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.147-1310_147-1309i others(3): Show |
VAMP7 | ENSG00000124333.16 | transcript | ENST00000286448.12 | protein_coding | 2/7 | chrX | 155894313 | ||||||
| chrX:155894358
|
C | A | 1 | a0001c0001t0001g0064 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.147-1265C>A | VAMP7 | ENSG00000124333.16 | transcript | ENST00000286448.12 | protein_coding | 2/7 | chrX | 155894358 | ||||||
| chrX:155894618
|
G | T | 1 | a0001c0001t0001g0032 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.147-1005G>T | VAMP7 | ENSG00000124333.16 | transcript | ENST00000286448.12 | protein_coding | 2/7 | chrX | 155894618 | ||||||
| chrX:155895406
|
G | A | 3 | a0001c0001t0001g0007a0001c0001t0001g0037a0001c0001t0001g0038 | 4 | HG01884.hp1 HG02257.hp2 HG02559.hp2 others(1): Show |
intron_variant | MODIFIER | c.147-217G>A | VAMP7 | ENSG00000124333.16 | transcript | ENST00000286448.12 | protein_coding | 2/7 | chrX | 155895406 | ||||||
| chrX:155895469
|
G | T | 1 | a0001c0001t0002g0137 | 1 | HG01257.hp2 | intron_variant | MODIFIER | c.147-154G>T | VAMP7 | ENSG00000124333.16 | transcript | ENST00000286448.12 | protein_coding | 2/7 | chrX | 155895469 | ||||||
| chrX:155895719
|
T | C | 1 | a0001c0001t0001g0090 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.204+39T>C | VAMP7 | ENSG00000124333.16 | transcript | ENST00000286448.12 | protein_coding | 3/7 | chrX | 155895719 | ||||||
| chrX:155895764
|
C | T | 1 | a0001c0001t0001g0080 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.204+84C>T | VAMP7 | ENSG00000124333.16 | transcript | ENST00000286448.12 | protein_coding | 3/7 | chrX | 155895764 | ||||||
| chrX:155895985
|
G | C | 2 | a0001c0001t0001g0021a0001c0001t0001g0022 | 2 | HG02132.hp2 NA19085.hp2 |
intron_variant | MODIFIER | c.204+305G>C | VAMP7 | ENSG00000124333.16 | transcript | ENST00000286448.12 | protein_coding | 3/7 | chrX | 155895985 | ||||||
| chrX:155895986
|
G | T | 2 | a0001c0001t0001g0021a0001c0001t0001g0022 | 2 | HG02132.hp2 NA19085.hp2 |
intron_variant | MODIFIER | c.204+306G>T | VAMP7 | ENSG00000124333.16 | transcript | ENST00000286448.12 | protein_coding | 3/7 | chrX | 155895986 | ||||||
| chrX:155896004
|
G | A | 1 | a0001c0001t0006g0018 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.204+324G>A | VAMP7 | ENSG00000124333.16 | transcript | ENST00000286448.12 | protein_coding | 3/7 | chrX | 155896004 | ||||||
| chrX:155896076
|
T | TG | 1 | a0001c0001t0001g0142 | 1 | NA19001.hp1 | intron_variant | MODIFIER | c.204+400dupG | VAMP7 | ENSG00000124333.16 | transcript | ENST00000286448.12 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chrX | 155896076 | |||||
| chrX:155896395
|
A | G | 96 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(93): Show | 114 | HG00099.hp2 HG00408.hp1 HG00558.hp2 others(111): Show |
intron_variant | MODIFIER | c.204+715A>G | VAMP7 | ENSG00000124333.16 | transcript | ENST00000286448.12 | protein_coding | 3/7 | chrX | 155896395 | ||||||
| chrX:155896474
|
CTGTT | C | 3 | a0001c0001t0001g0002a0001c0001t0001g0060a0001c0001t0001g0153 | 6 | HG02109.hp1 HG02280.hp1 HG02976.hp1 others(3): Show |
intron_variant | MODIFIER | c.204+798_204+801del others(4): Show |
VAMP7 | ENSG00000124333.16 | transcript | ENST00000286448.12 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chrX | 155896474 | |||||
| chrX:155896552
|
C | T | 4 | a0001c0001t0001g0064a0001c0001t0001g0078a0001c0001t0001g0079others(1): Show | 4 | HG00621.hp1 NA18945.hp1 NA19001.hp1 others(1): Show |
intron_variant | MODIFIER | c.204+872C>T | VAMP7 | ENSG00000124333.16 | transcript | ENST00000286448.12 | protein_coding | 3/7 | chrX | 155896552 | ||||||
| chrX:155896812
|
C | T | 8 | a0001c0001t0001g0012a0001c0001t0001g0029a0001c0001t0001g0042others(5): Show | 9 | HG01884.hp2 HG02109.hp2 HG02622.hp1 others(6): Show |
intron_variant | MODIFIER | c.204+1132C>T | VAMP7 | ENSG00000124333.16 | transcript | ENST00000286448.12 | protein_coding | 3/7 | chrX | 155896812 | ||||||
| chrX:155896874
|
CT | C | 1 | a0001c0001t0001g0154 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.204+1201delT | VAMP7 | ENSG00000124333.16 | transcript | ENST00000286448.12 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chrX | 155896874 | |||||
| chrX:155896940
|
C | T | 1 | a0001c0001t0004g0020 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.205-1172C>T | VAMP7 | ENSG00000124333.16 | transcript | ENST00000286448.12 | protein_coding | 3/7 | chrX | 155896940 | ||||||
| chrX:155897243
|
CTTT | C | 1 | a0001c0001t0001g0154 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.205-864_205-862del others(3): Show |
VAMP7 | ENSG00000124333.16 | transcript | ENST00000286448.12 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chrX | 155897243 | |||||
| chrX:155897373
|
T | C | 1 | a0001c0001t0001g0158 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.205-739T>C | VAMP7 | ENSG00000124333.16 | transcript | ENST00000286448.12 | protein_coding | 3/7 | chrX | 155897373 | ||||||
| chrX:155897377
|
T | C | 1 | a0001c0001t0001g0145 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.205-735T>C | VAMP7 | ENSG00000124333.16 | transcript | ENST00000286448.12 | protein_coding | 3/7 | chrX | 155897377 | ||||||
| chrX:155897532
|
C | G | 4 | a0001c0001t0001g0021a0001c0001t0001g0022a0001c0001t0001g0023others(1): Show | 4 | HG02132.hp2 HG02886.hp2 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.205-580C>G | VAMP7 | ENSG00000124333.16 | transcript | ENST00000286448.12 | protein_coding | 3/7 | chrX | 155897532 | ||||||
| chrX:155897552
|
A | C | 1 | a0001c0001t0001g0158 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.205-560A>C | VAMP7 | ENSG00000124333.16 | transcript | ENST00000286448.12 | protein_coding | 3/7 | chrX | 155897552 | ||||||
| chrX:155897736
|
T | C | 3 | a0001c0002t0001g0026a0001c0002t0001g0027a0001c0002t0001g0028 | 3 | HG02630.hp2 HG02922.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.205-376T>C | VAMP7 | ENSG00000124333.16 | transcript | ENST00000286448.12 | protein_coding | 3/7 | chrX | 155897736 | ||||||
| chrX:155897792
|
A | T | 1 | a0001c0001t0001g0089 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.205-320A>T | VAMP7 | ENSG00000124333.16 | transcript | ENST00000286448.12 | protein_coding | 3/7 | chrX | 155897792 | ||||||
| chrX:155898011
|
A | G | 97 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(94): Show | 115 | HG00099.hp2 HG00408.hp1 HG00558.hp2 others(112): Show |
intron_variant | MODIFIER | c.205-101A>G | VAMP7 | ENSG00000124333.16 | transcript | ENST00000286448.12 | protein_coding | 3/7 | chrX | 155898011 | ||||||
| chrX:155898104
|
CT | C | 1 | a0001c0001t0001g0065 | 1 | NA19072.hp1 | splice_region_variant&intron_variant | LOW | c.205-4delT | VAMP7 | ENSG00000124333.16 | transcript | ENST00000286448.12 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chrX | 155898104 | |||||
| chrX:155898390
|
TA | T | 4 | a0001c0001t0001g0019a0001c0001t0001g0023a0001c0001t0001g0158others(1): Show | 4 | HG01070.hp2 HG02622.hp2 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.342+151delA | VAMP7 | ENSG00000124333.16 | transcript | ENST00000286448.12 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chrX | 155898390 | |||||
| chrX:155898645
|
A | T | 96 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(93): Show | 114 | HG00099.hp2 HG00408.hp1 HG00558.hp2 others(111): Show |
intron_variant | MODIFIER | c.342+396A>T | VAMP7 | ENSG00000124333.16 | transcript | ENST00000286448.12 | protein_coding | 4/7 | chrX | 155898645 | ||||||
| chrX:155898739
|
G | A | 1 | a0001c0001t0006g0018 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.342+490G>A | VAMP7 | ENSG00000124333.16 | transcript | ENST00000286448.12 | protein_coding | 4/7 | chrX | 155898739 | ||||||
| chrX:155898754
|
T | C | 1 | a0001c0001t0006g0018 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.342+505T>C | VAMP7 | ENSG00000124333.16 | transcript | ENST00000286448.12 | protein_coding | 4/7 | chrX | 155898754 | ||||||
| chrX:155898798
|
G | T | 100 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(97): Show | 118 | HG00099.hp2 HG00408.hp1 HG00558.hp2 others(115): Show |
intron_variant | MODIFIER | c.342+549G>T | VAMP7 | ENSG00000124333.16 | transcript | ENST00000286448.12 | protein_coding | 4/7 | chrX | 155898798 | ||||||
| chrX:155898836
|
C | T | 100 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(97): Show | 118 | HG00099.hp2 HG00408.hp1 HG00558.hp2 others(115): Show |
intron_variant | MODIFIER | c.342+587C>T | VAMP7 | ENSG00000124333.16 | transcript | ENST00000286448.12 | protein_coding | 4/7 | chrX | 155898836 | ||||||
| chrX:155898872
|
A | G | 1 | a0001c0001t0001g0158 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.342+623A>G | VAMP7 | ENSG00000124333.16 | transcript | ENST00000286448.12 | protein_coding | 4/7 | chrX | 155898872 | ||||||
| chrX:155898879
|
C | G | 3 | a0001c0001t0001g0050a0001c0001t0001g0055a0001c0001t0001g0056 | 3 | HG01071.hp1 HG01081.hp1 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.342+630C>G | VAMP7 | ENSG00000124333.16 | transcript | ENST00000286448.12 | protein_coding | 4/7 | chrX | 155898879 | ||||||
| chrX:155898958
|
T | C | 1 | a0001c0001t0006g0018 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.342+709T>C | VAMP7 | ENSG00000124333.16 | transcript | ENST00000286448.12 | protein_coding | 4/7 | chrX | 155898958 | ||||||
| chrX:155898959
|
G | T | 1 | a0001c0001t0001g0023 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.342+710G>T | VAMP7 | ENSG00000124333.16 | transcript | ENST00000286448.12 | protein_coding | 4/7 | chrX | 155898959 | ||||||
| chrX:155899129
|
T | C | 100 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(97): Show | 118 | HG00099.hp2 HG00408.hp1 HG00558.hp2 others(115): Show |
intron_variant | MODIFIER | c.342+880T>C | VAMP7 | ENSG00000124333.16 | transcript | ENST00000286448.12 | protein_coding | 4/7 | chrX | 155899129 | ||||||
| chrX:155899344
|
T | C | 2 | a0001c0001t0001g0019a0001c0001t0006g0018 | 2 | HG01070.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.342+1095T>C | VAMP7 | ENSG00000124333.16 | transcript | ENST00000286448.12 | protein_coding | 4/7 | chrX | 155899344 | ||||||
| chrX:155899390
|
G | A | 1 | a0001c0001t0001g0033 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.343-1107G>A | VAMP7 | ENSG00000124333.16 | transcript | ENST00000286448.12 | protein_coding | 4/7 | chrX | 155899390 | ||||||
| chrX:155899415
|
T | C | 3 | a0001c0002t0001g0026a0001c0002t0001g0027a0001c0002t0001g0028 | 3 | HG02630.hp2 HG02922.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.343-1082T>C | VAMP7 | ENSG00000124333.16 | transcript | ENST00000286448.12 | protein_coding | 4/7 | chrX | 155899415 | ||||||
| chrX:155899417
|
G | A | 5 | a0001c0001t0001g0012a0001c0001t0001g0029a0001c0001t0001g0042others(2): Show | 6 | HG01884.hp2 HG02109.hp2 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.343-1080G>A | VAMP7 | ENSG00000124333.16 | transcript | ENST00000286448.12 | protein_coding | 4/7 | chrX | 155899417 | ||||||
| chrX:155899440
|
C | T | 1 | a0001c0001t0001g0151 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.343-1057C>T | VAMP7 | ENSG00000124333.16 | transcript | ENST00000286448.12 | protein_coding | 4/7 | chrX | 155899440 | ||||||
| chrX:155899460
|
TA | T | 2 | a0001c0001t0001g0065a0001c0001t0001g0109 | 2 | NA18968.hp2 NA19072.hp1 |
intron_variant | MODIFIER | c.343-1029delA | VAMP7 | ENSG00000124333.16 | transcript | ENST00000286448.12 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chrX | 155899460 | |||||
| chrX:155899542
|
G | GCA | 96 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(93): Show | 114 | HG00099.hp2 HG00408.hp1 HG00558.hp2 others(111): Show |
intron_variant | MODIFIER | c.343-941_343-940dup others(2): Show |
VAMP7 | ENSG00000124333.16 | transcript | ENST00000286448.12 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chrX | 155899542 | |||||
| chrX:155899645
|
T | A | 4 | a0001c0001t0001g0099a0001c0001t0001g0100a0001c0001t0001g0101others(1): Show | 4 | HG02257.hp1 HG02280.hp2 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.343-852T>A | VAMP7 | ENSG00000124333.16 | transcript | ENST00000286448.12 | protein_coding | 4/7 | chrX | 155899645 | ||||||
| chrX:155899668
|
G | A | 102 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(99): Show | 120 | HG00099.hp2 HG00408.hp1 HG00558.hp2 others(117): Show |
intron_variant | MODIFIER | c.343-829G>A | VAMP7 | ENSG00000124333.16 | transcript | ENST00000286448.12 | protein_coding | 4/7 | chrX | 155899668 | ||||||
| chrX:155899680
|
G | A | 101 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(98): Show | 119 | HG00099.hp2 HG00408.hp1 HG00558.hp2 others(116): Show |
intron_variant | MODIFIER | c.343-817G>A | VAMP7 | ENSG00000124333.16 | transcript | ENST00000286448.12 | protein_coding | 4/7 | chrX | 155899680 | ||||||
| chrX:155900050
|
C | T | 1 | a0001c0001t0001g0095 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.343-447C>T | VAMP7 | ENSG00000124333.16 | transcript | ENST00000286448.12 | protein_coding | 4/7 | chrX | 155900050 | ||||||
| chrX:155900320
|
GC | G | 1 | a0001c0001t0001g0109 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.343-174delC | VAMP7 | ENSG00000124333.16 | transcript | ENST00000286448.12 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chrX | 155900320 | |||||
| chrX:155901127
|
C | G | 1 | a0001c0001t0001g0150 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.433+540C>G | VAMP7 | ENSG00000124333.16 | transcript | ENST00000286448.12 | protein_coding | 5/7 | chrX | 155901127 | ||||||
| chrX:155901193
|
A | T | 1 | a0001c0001t0001g0158 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.433+606A>T | VAMP7 | ENSG00000124333.16 | transcript | ENST00000286448.12 | protein_coding | 5/7 | chrX | 155901193 | ||||||
| chrX:155901199
|
A | G | 95 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(92): Show | 113 | HG00099.hp2 HG00408.hp1 HG00558.hp2 others(110): Show |
intron_variant | MODIFIER | c.433+612A>G | VAMP7 | ENSG00000124333.16 | transcript | ENST00000286448.12 | protein_coding | 5/7 | chrX | 155901199 | ||||||
| chrX:155901224
|
C | T | 4 | a0001c0001t0001g0002a0001c0001t0001g0060a0001c0001t0001g0062others(1): Show | 7 | HG01891.hp1 HG02109.hp1 HG02280.hp1 others(4): Show |
intron_variant | MODIFIER | c.433+637C>T | VAMP7 | ENSG00000124333.16 | transcript | ENST00000286448.12 | protein_coding | 5/7 | chrX | 155901224 | ||||||
| chrX:155901358
|
TC | T | 4 | a0001c0001t0001g0002a0001c0001t0001g0060a0001c0001t0001g0062others(1): Show | 7 | HG01891.hp1 HG02109.hp1 HG02280.hp1 others(4): Show |
intron_variant | MODIFIER | c.433+772delC | VAMP7 | ENSG00000124333.16 | transcript | ENST00000286448.12 | protein_coding | 5/7 | chrX | 155901358 | ||||||
| chrX:155901384
|
A | T | 1 | a0001c0001t0001g0012 | 2 | HG02109.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.433+797A>T | VAMP7 | ENSG00000124333.16 | transcript | ENST00000286448.12 | protein_coding | 5/7 | chrX | 155901384 | ||||||
| chrX:155901435
|
A | G | 2 | a0001c0001t0001g0114a0001c0001t0001g0124 | 2 | HG00597.hp2 NA18988.hp1 |
intron_variant | MODIFIER | c.433+848A>G | VAMP7 | ENSG00000124333.16 | transcript | ENST00000286448.12 | protein_coding | 5/7 | chrX | 155901435 | ||||||
| chrX:155901521
|
T | A | 3 | a0001c0001t0001g0007a0001c0001t0001g0037a0001c0001t0001g0038 | 4 | HG01884.hp1 HG02257.hp2 HG02559.hp2 others(1): Show |
intron_variant | MODIFIER | c.433+934T>A | VAMP7 | ENSG00000124333.16 | transcript | ENST00000286448.12 | protein_coding | 5/7 | chrX | 155901521 | ||||||
| chrX:155901706
|
G | C | 92 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(89): Show | 110 | HG00099.hp2 HG00408.hp1 HG00558.hp2 others(107): Show |
intron_variant | MODIFIER | c.433+1119G>C | VAMP7 | ENSG00000124333.16 | transcript | ENST00000286448.12 | protein_coding | 5/7 | chrX | 155901706 | ||||||
| chrX:155901917
|
T | C | 1 | a0001c0001t0001g0155 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.433+1330T>C | VAMP7 | ENSG00000124333.16 | transcript | ENST00000286448.12 | protein_coding | 5/7 | chrX | 155901917 | ||||||
| chrX:155902004
|
A | C | 94 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(91): Show | 112 | HG00099.hp2 HG00408.hp1 HG00558.hp2 others(109): Show |
intron_variant | MODIFIER | c.433+1417A>C | VAMP7 | ENSG00000124333.16 | transcript | ENST00000286448.12 | protein_coding | 5/7 | chrX | 155902004 | ||||||
| chrX:155902006
|
A | T | 1 | a0001c0001t0003g0116 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.433+1419A>T | VAMP7 | ENSG00000124333.16 | transcript | ENST00000286448.12 | protein_coding | 5/7 | chrX | 155902006 | ||||||
| chrX:155902011
|
A | G | 1 | a0001c0001t0001g0128 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.433+1424A>G | VAMP7 | ENSG00000124333.16 | transcript | ENST00000286448.12 | protein_coding | 5/7 | chrX | 155902011 | ||||||
| chrX:155902039
|
T | C | 1 | a0001c0001t0001g0076 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.433+1452T>C | VAMP7 | ENSG00000124333.16 | transcript | ENST00000286448.12 | protein_coding | 5/7 | chrX | 155902039 | ||||||
| chrX:155902173
|
C | T | 101 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(98): Show | 119 | HG00099.hp2 HG00408.hp1 HG00558.hp2 others(116): Show |
intron_variant | MODIFIER | c.433+1586C>T | VAMP7 | ENSG00000124333.16 | transcript | ENST00000286448.12 | protein_coding | 5/7 | chrX | 155902173 | ||||||
| chrX:155902256
|
A | G | 1 | a0001c0001t0001g0073 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.433+1669A>G | VAMP7 | ENSG00000124333.16 | transcript | ENST00000286448.12 | protein_coding | 5/7 | chrX | 155902256 | ||||||
| chrX:155902316
|
A | G | 92 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(89): Show | 110 | HG00099.hp2 HG00408.hp1 HG00558.hp2 others(107): Show |
intron_variant | MODIFIER | c.433+1729A>G | VAMP7 | ENSG00000124333.16 | transcript | ENST00000286448.12 | protein_coding | 5/7 | chrX | 155902316 | ||||||
| chrX:155902407
|
T | C | 102 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(99): Show | 120 | HG00099.hp2 HG00408.hp1 HG00558.hp2 others(117): Show |
intron_variant | MODIFIER | c.433+1820T>C | VAMP7 | ENSG00000124333.16 | transcript | ENST00000286448.12 | protein_coding | 5/7 | chrX | 155902407 | ||||||
| chrX:155902470
|
G | GT | 1 | a0001c0001t0001g0152 | 1 | NA18992.hp1 | intron_variant | MODIFIER | c.433+1888dupT | VAMP7 | ENSG00000124333.16 | transcript | ENST00000286448.12 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chrX | 155902470 | |||||
| chrX:155902616
|
A | G | 1 | a0001c0001t0004g0020 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.433+2029A>G | VAMP7 | ENSG00000124333.16 | transcript | ENST00000286448.12 | protein_coding | 5/7 | chrX | 155902616 | ||||||
| chrX:155902697
|
C | T | 1 | a0001c0001t0001g0019 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.433+2110C>T | VAMP7 | ENSG00000124333.16 | transcript | ENST00000286448.12 | protein_coding | 5/7 | chrX | 155902697 | ||||||
| chrX:155902737
|
T | A | 4 | a0001c0001t0001g0024a0001c0001t0001g0025a0001c0001t0001g0158others(1): Show | 4 | HG02622.hp2 HG02723.hp2 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.433+2150T>A | VAMP7 | ENSG00000124333.16 | transcript | ENST00000286448.12 | protein_coding | 5/7 | chrX | 155902737 | ||||||
| chrX:155902809
|
A | G | 94 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(91): Show | 112 | HG00099.hp2 HG00408.hp1 HG00558.hp2 others(109): Show |
intron_variant | MODIFIER | c.433+2222A>G | VAMP7 | ENSG00000124333.16 | transcript | ENST00000286448.12 | protein_coding | 5/7 | chrX | 155902809 | ||||||
| chrX:155902966
|
C | G | 1 | a0001c0001t0001g0023 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.433+2379C>G | VAMP7 | ENSG00000124333.16 | transcript | ENST00000286448.12 | protein_coding | 5/7 | chrX | 155902966 | ||||||
| chrX:155903050
|
T | C | 1 | a0001c0001t0001g0111 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.433+2463T>C | VAMP7 | ENSG00000124333.16 | transcript | ENST00000286448.12 | protein_coding | 5/7 | chrX | 155903050 | ||||||
| chrX:155903113
|
G | A | 1 | a0001c0001t0001g0146 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.433+2526G>A | VAMP7 | ENSG00000124333.16 | transcript | ENST00000286448.12 | protein_coding | 5/7 | chrX | 155903113 | ||||||
| chrX:155903205
|
C | G | 6 | a0001c0001t0001g0064a0001c0001t0001g0072a0001c0001t0001g0078others(3): Show | 6 | HG00597.hp2 HG00621.hp1 NA18945.hp1 others(3): Show |
intron_variant | MODIFIER | c.433+2618C>G | VAMP7 | ENSG00000124333.16 | transcript | ENST00000286448.12 | protein_coding | 5/7 | chrX | 155903205 | ||||||
| chrX:155903356
|
C | G | 1 | a0001c0001t0001g0062 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.433+2769C>G | VAMP7 | ENSG00000124333.16 | transcript | ENST00000286448.12 | protein_coding | 5/7 | chrX | 155903356 | ||||||
| chrX:155903413
|
C | T | 1 | a0001c0001t0001g0008 | 2 | HG01168.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.433+2826C>T | VAMP7 | ENSG00000124333.16 | transcript | ENST00000286448.12 | protein_coding | 5/7 | chrX | 155903413 | ||||||
| chrX:155903557
|
A | G | 4 | a0001c0001t0001g0158a0001c0002t0001g0026a0001c0002t0001g0027others(1): Show | 4 | HG02622.hp2 HG02630.hp2 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.433+2970A>G | VAMP7 | ENSG00000124333.16 | transcript | ENST00000286448.12 | protein_coding | 5/7 | chrX | 155903557 | ||||||
| chrX:155903733
|
T | C | 2 | a0001c0001t0001g0024a0001c0001t0001g0025 | 2 | HG02723.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.433+3146T>C | VAMP7 | ENSG00000124333.16 | transcript | ENST00000286448.12 | protein_coding | 5/7 | chrX | 155903733 | ||||||
| chrX:155903750
|
A | T | 1 | a0001c0001t0001g0076 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.433+3163A>T | VAMP7 | ENSG00000124333.16 | transcript | ENST00000286448.12 | protein_coding | 5/7 | chrX | 155903750 | ||||||
| chrX:155903779
|
C | A | 96 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(93): Show | 114 | HG00099.hp2 HG00408.hp1 HG00558.hp2 others(111): Show |
intron_variant | MODIFIER | c.433+3192C>A | VAMP7 | ENSG00000124333.16 | transcript | ENST00000286448.12 | protein_coding | 5/7 | chrX | 155903779 | ||||||
| chrX:155903898
|
A | G | 1 | a0001c0001t0001g0143 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.433+3311A>G | VAMP7 | ENSG00000124333.16 | transcript | ENST00000286448.12 | protein_coding | 5/7 | chrX | 155903898 | ||||||
| chrX:155903920
|
G | A | 3 | a0001c0002t0001g0026a0001c0002t0001g0027a0001c0002t0001g0028 | 3 | HG02630.hp2 HG02922.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.433+3333G>A | VAMP7 | ENSG00000124333.16 | transcript | ENST00000286448.12 | protein_coding | 5/7 | chrX | 155903920 | ||||||
| chrX:155903957
|
A | C | 1 | a0001c0001t0001g0115 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.433+3370A>C | VAMP7 | ENSG00000124333.16 | transcript | ENST00000286448.12 | protein_coding | 5/7 | chrX | 155903957 | ||||||
| chrX:155904082
|
A | C | 1 | a0001c0001t0006g0018 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.433+3495A>C | VAMP7 | ENSG00000124333.16 | transcript | ENST00000286448.12 | protein_coding | 5/7 | chrX | 155904082 | ||||||
| chrX:155904089
|
G | A | 5 | a0001c0001t0001g0024a0001c0001t0001g0025a0001c0001t0001g0158others(2): Show | 5 | HG02622.hp2 HG02723.hp2 HG03195.hp1 others(2): Show |
intron_variant | MODIFIER | c.433+3502G>A | VAMP7 | ENSG00000124333.16 | transcript | ENST00000286448.12 | protein_coding | 5/7 | chrX | 155904089 | ||||||
| chrX:155904098
|
C | T | 1 | a0001c0001t0001g0022 | 1 | NA19085.hp2 | intron_variant | MODIFIER | c.433+3511C>T | VAMP7 | ENSG00000124333.16 | transcript | ENST00000286448.12 | protein_coding | 5/7 | chrX | 155904098 | ||||||
| chrX:155904121
|
C | T | 1 | a0001c0001t0001g0108 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.433+3534C>T | VAMP7 | ENSG00000124333.16 | transcript | ENST00000286448.12 | protein_coding | 5/7 | chrX | 155904121 | ||||||
| chrX:155904124
|
A | G | 1 | a0001c0001t0001g0158 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.433+3537A>G | VAMP7 | ENSG00000124333.16 | transcript | ENST00000286448.12 | protein_coding | 5/7 | chrX | 155904124 | ||||||
| chrX:155904210
|
T | TG | 1 | a0001c0001t0001g0063 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.433+3629dupG | VAMP7 | ENSG00000124333.16 | transcript | ENST00000286448.12 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chrX | 155904210 | |||||
| chrX:155904360
|
T | G | 1 | a0001c0001t0001g0032 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.433+3773T>G | VAMP7 | ENSG00000124333.16 | transcript | ENST00000286448.12 | protein_coding | 5/7 | chrX | 155904360 | ||||||
| chrX:155904376
|
A | AAAAC | 101 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(98): Show | 119 | HG00099.hp2 HG00408.hp1 HG00558.hp2 others(116): Show |
intron_variant | MODIFIER | c.433+3790_433+3791i others(6): Show |
VAMP7 | ENSG00000124333.16 | transcript | ENST00000286448.12 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chrX | 155904376 | |||||
| chrX:155904524
|
A | G | 1 | a0001c0001t0001g0132 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.433+3937A>G | VAMP7 | ENSG00000124333.16 | transcript | ENST00000286448.12 | protein_coding | 5/7 | chrX | 155904524 | ||||||
| chrX:155904532
|
G | A | 101 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(98): Show | 119 | HG00099.hp2 HG00408.hp1 HG00558.hp2 others(116): Show |
intron_variant | MODIFIER | c.433+3945G>A | VAMP7 | ENSG00000124333.16 | transcript | ENST00000286448.12 | protein_coding | 5/7 | chrX | 155904532 | ||||||
| chrX:155904689
|
T | A | 1 | a0001c0001t0001g0148 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.433+4102T>A | VAMP7 | ENSG00000124333.16 | transcript | ENST00000286448.12 | protein_coding | 5/7 | chrX | 155904689 | ||||||
| chrX:155904706
|
G | C | 3 | a0001c0002t0001g0026a0001c0002t0001g0027a0001c0002t0001g0028 | 3 | HG02630.hp2 HG02922.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.433+4119G>C | VAMP7 | ENSG00000124333.16 | transcript | ENST00000286448.12 | protein_coding | 5/7 | chrX | 155904706 | ||||||
| chrX:155904778
|
C | A | 3 | a0001c0001t0001g0023a0001c0001t0001g0158a0001c0001t0004g0020 | 3 | HG02622.hp2 HG02886.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.433+4191C>A | VAMP7 | ENSG00000124333.16 | transcript | ENST00000286448.12 | protein_coding | 5/7 | chrX | 155904778 | ||||||
| chrX:155904906
|
TTA | T | 99 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(96): Show | 117 | HG00099.hp2 HG00408.hp1 HG00558.hp2 others(114): Show |
intron_variant | MODIFIER | c.433+4335_433+4336d others(4): Show |
VAMP7 | ENSG00000124333.16 | transcript | ENST00000286448.12 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chrX | 155904906 | |||||
| chrX:155904906
|
TTATA | T | 1 | a0001c0001t0006g0018 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.433+4333_433+4336d others(6): Show |
VAMP7 | ENSG00000124333.16 | transcript | ENST00000286448.12 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chrX | 155904906 | |||||
| chrX:155904975
|
G | A | 1 | a0001c0001t0004g0020 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.433+4388G>A | VAMP7 | ENSG00000124333.16 | transcript | ENST00000286448.12 | protein_coding | 5/7 | chrX | 155904975 | ||||||
| chrX:155905046
|
G | A | 3 | a0001c0001t0001g0039a0001c0001t0001g0045a0001c0001t0001g0046 | 3 | HG01081.hp2 HG03491.hp2 HG04184.hp2 |
intron_variant | MODIFIER | c.433+4459G>A | VAMP7 | ENSG00000124333.16 | transcript | ENST00000286448.12 | protein_coding | 5/7 | chrX | 155905046 | ||||||
| chrX:155905143
|
AT | A | 1 | a0001c0001t0001g0019 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.433+4559delT | VAMP7 | ENSG00000124333.16 | transcript | ENST00000286448.12 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chrX | 155905143 | |||||
| chrX:155905462
|
CAT | C | 1 | a0001c0001t0001g0040 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.433+4878_433+4879d others(4): Show |
VAMP7 | ENSG00000124333.16 | transcript | ENST00000286448.12 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chrX | 155905462 | |||||
| chrX:155905840
|
T | C | 5 | a0001c0001t0001g0023a0001c0001t0001g0024a0001c0001t0001g0025others(2): Show | 5 | HG02622.hp2 HG02723.hp2 HG02886.hp2 others(2): Show |
intron_variant | MODIFIER | c.433+5253T>C | VAMP7 | ENSG00000124333.16 | transcript | ENST00000286448.12 | protein_coding | 5/7 | chrX | 155905840 | ||||||
| chrX:155905978
|
A | AG | 159 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(156): Show | 183 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(180): Show |
intron_variant | MODIFIER | c.433+5394dupG | VAMP7 | ENSG00000124333.16 | transcript | ENST00000286448.12 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chrX | 155905978 | |||||
| chrX:155906044
|
G | GT | 159 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(156): Show | 183 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(180): Show |
intron_variant | MODIFIER | c.433+5460dupT | VAMP7 | ENSG00000124333.16 | transcript | ENST00000286448.12 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chrX | 155906044 | |||||
| chrX:155906254
|
A | G | 1 | a0001c0001t0001g0023 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.433+5667A>G | VAMP7 | ENSG00000124333.16 | transcript | ENST00000286448.12 | protein_coding | 5/7 | chrX | 155906254 | ||||||
| chrX:155906261
|
T | A | 97 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(94): Show | 115 | HG00099.hp2 HG00408.hp1 HG00558.hp2 others(112): Show |
intron_variant | MODIFIER | c.433+5674T>A | VAMP7 | ENSG00000124333.16 | transcript | ENST00000286448.12 | protein_coding | 5/7 | chrX | 155906261 | ||||||
| chrX:155906497
|
T | A | 91 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(88): Show | 109 | HG00099.hp2 HG00408.hp1 HG00558.hp2 others(106): Show |
intron_variant | MODIFIER | c.433+5910T>A | VAMP7 | ENSG00000124333.16 | transcript | ENST00000286448.12 | protein_coding | 5/7 | chrX | 155906497 | ||||||
| chrX:155906564
|
G | A | 1 | a0001c0001t0001g0124 | 1 | NA18988.hp1 | intron_variant | MODIFIER | c.433+5977G>A | VAMP7 | ENSG00000124333.16 | transcript | ENST00000286448.12 | protein_coding | 5/7 | chrX | 155906564 | ||||||
| chrX:155906586
|
A | G | 93 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(90): Show | 111 | HG00099.hp2 HG00408.hp1 HG00558.hp2 others(108): Show |
intron_variant | MODIFIER | c.433+5999A>G | VAMP7 | ENSG00000124333.16 | transcript | ENST00000286448.12 | protein_coding | 5/7 | chrX | 155906586 | ||||||
| chrX:155906610
|
G | A | 1 | a0001c0001t0001g0158 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.433+6023G>A | VAMP7 | ENSG00000124333.16 | transcript | ENST00000286448.12 | protein_coding | 5/7 | chrX | 155906610 | ||||||
| chrX:155906632
|
A | G | 1 | a0001c0001t0001g0085 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.433+6045A>G | VAMP7 | ENSG00000124333.16 | transcript | ENST00000286448.12 | protein_coding | 5/7 | chrX | 155906632 | ||||||
| chrX:155906685
|
C | A | 101 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(98): Show | 119 | HG00099.hp2 HG00408.hp1 HG00558.hp2 others(116): Show |
intron_variant | MODIFIER | c.433+6098C>A | VAMP7 | ENSG00000124333.16 | transcript | ENST00000286448.12 | protein_coding | 5/7 | chrX | 155906685 | ||||||
| chrX:155906731
|
C | T | 1 | a0001c0001t0001g0071 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.433+6144C>T | VAMP7 | ENSG00000124333.16 | transcript | ENST00000286448.12 | protein_coding | 5/7 | chrX | 155906731 | ||||||
| chrX:155906785
|
G | A | 101 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(98): Show | 119 | HG00099.hp2 HG00408.hp1 HG00558.hp2 others(116): Show |
intron_variant | MODIFIER | c.433+6198G>A | VAMP7 | ENSG00000124333.16 | transcript | ENST00000286448.12 | protein_coding | 5/7 | chrX | 155906785 | ||||||
| chrX:155906818
|
T | A | 101 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(98): Show | 119 | HG00099.hp2 HG00408.hp1 HG00558.hp2 others(116): Show |
intron_variant | MODIFIER | c.433+6231T>A | VAMP7 | ENSG00000124333.16 | transcript | ENST00000286448.12 | protein_coding | 5/7 | chrX | 155906818 | ||||||
| chrX:155906831
|
G | A | 1 | a0001c0001t0006g0018 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.433+6244G>A | VAMP7 | ENSG00000124333.16 | transcript | ENST00000286448.12 | protein_coding | 5/7 | chrX | 155906831 | ||||||
| chrX:155906944
|
G | T | 1 | a0001c0001t0001g0011 | 2 | NA18953.hp2 NA19079.hp1 |
intron_variant | MODIFIER | c.433+6357G>T | VAMP7 | ENSG00000124333.16 | transcript | ENST00000286448.12 | protein_coding | 5/7 | chrX | 155906944 | ||||||
| chrX:155907036
|
A | AT | 1 | a0001c0001t0001g0085 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.433+6457dupT | VAMP7 | ENSG00000124333.16 | transcript | ENST00000286448.12 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chrX | 155907036 | |||||
| chrX:155907480
|
C | T | 30 | a0001c0001t0001g0004a0001c0001t0001g0009a0001c0001t0001g0010others(27): Show | 35 | HG00558.hp2 HG00597.hp1 HG00621.hp1 others(32): Show |
intron_variant | MODIFIER | c.433+6893C>T | VAMP7 | ENSG00000124333.16 | transcript | ENST00000286448.12 | protein_coding | 5/7 | chrX | 155907480 | ||||||
| chrX:155907481
|
G | A | 1 | a0001c0001t0001g0052 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.433+6894G>A | VAMP7 | ENSG00000124333.16 | transcript | ENST00000286448.12 | protein_coding | 5/7 | chrX | 155907481 | ||||||
| chrX:155907519
|
TC | T | 90 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(87): Show | 108 | HG00099.hp2 HG00408.hp1 HG00558.hp2 others(105): Show |
intron_variant | MODIFIER | c.433+6933delC | VAMP7 | ENSG00000124333.16 | transcript | ENST00000286448.12 | protein_coding | 5/7 | chrX | 155907519 | ||||||
| chrX:155907679
|
T | A | 2 | a0001c0001t0001g0019a0001c0001t0006g0018 | 2 | HG01070.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.433+7092T>A | VAMP7 | ENSG00000124333.16 | transcript | ENST00000286448.12 | protein_coding | 5/7 | chrX | 155907679 | ||||||
| chrX:155907808
|
G | A | 2 | a0001c0001t0001g0024a0001c0001t0001g0025 | 2 | HG02723.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.433+7221G>A | VAMP7 | ENSG00000124333.16 | transcript | ENST00000286448.12 | protein_coding | 5/7 | chrX | 155907808 | ||||||
| chrX:155907847
|
C | T | 1 | a0001c0001t0001g0040 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.433+7260C>T | VAMP7 | ENSG00000124333.16 | transcript | ENST00000286448.12 | protein_coding | 5/7 | chrX | 155907847 | ||||||
| chrX:155907854
|
C | T | 1 | a0001c0001t0001g0094 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.433+7267C>T | VAMP7 | ENSG00000124333.16 | transcript | ENST00000286448.12 | protein_coding | 5/7 | chrX | 155907854 | ||||||
| chrX:155907963
|
C | T | 3 | a0001c0001t0001g0087a0001c0001t0001g0088a0001c0001t0001g0089 | 3 | NA18967.hp1 NA18989.hp2 NA18998.hp2 |
intron_variant | MODIFIER | c.433+7376C>T | VAMP7 | ENSG00000124333.16 | transcript | ENST00000286448.12 | protein_coding | 5/7 | chrX | 155907963 | ||||||
| chrX:155907984
|
C | G | 2 | a0001c0001t0001g0039a0001c0001t0001g0045 | 2 | HG01081.hp2 HG04184.hp2 |
intron_variant | MODIFIER | c.433+7397C>G | VAMP7 | ENSG00000124333.16 | transcript | ENST00000286448.12 | protein_coding | 5/7 | chrX | 155907984 | ||||||
| chrX:155908003
|
C | T | 1 | a0001c0001t0001g0029 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.433+7416C>T | VAMP7 | ENSG00000124333.16 | transcript | ENST00000286448.12 | protein_coding | 5/7 | chrX | 155908003 | ||||||
| chrX:155908043
|
C | T | 1 | a0001c0001t0001g0048 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.433+7456C>T | VAMP7 | ENSG00000124333.16 | transcript | ENST00000286448.12 | protein_coding | 5/7 | chrX | 155908043 | ||||||
| chrX:155908057
|
C | T | 91 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(88): Show | 109 | HG00099.hp2 HG00408.hp1 HG00558.hp2 others(106): Show |
intron_variant | MODIFIER | c.433+7470C>T | VAMP7 | ENSG00000124333.16 | transcript | ENST00000286448.12 | protein_coding | 5/7 | chrX | 155908057 | ||||||
| chrX:155908151
|
C | CG | 1 | a0001c0001t0001g0048 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.433+7568dupG | VAMP7 | ENSG00000124333.16 | transcript | ENST00000286448.12 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chrX | 155908151 | |||||
| chrX:155908219
|
G | A | 1 | a0001c0001t0006g0018 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.433+7632G>A | VAMP7 | ENSG00000124333.16 | transcript | ENST00000286448.12 | protein_coding | 5/7 | chrX | 155908219 | ||||||
| chrX:155908264
|
G | A | 1 | a0001c0001t0001g0115 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.433+7677G>A | VAMP7 | ENSG00000124333.16 | transcript | ENST00000286448.12 | protein_coding | 5/7 | chrX | 155908264 | ||||||
| chrX:155908294
|
C | T | 4 | a0001c0001t0001g0148a0001c0001t0001g0149a0001c0001t0001g0151others(1): Show | 4 | HG00280.hp1 NA18992.hp1 NA18998.hp1 others(1): Show |
intron_variant | MODIFIER | c.433+7707C>T | VAMP7 | ENSG00000124333.16 | transcript | ENST00000286448.12 | protein_coding | 5/7 | chrX | 155908294 | ||||||
| chrX:155908315
|
G | A | 1 | a0001c0001t0001g0115 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.433+7728G>A | VAMP7 | ENSG00000124333.16 | transcript | ENST00000286448.12 | protein_coding | 5/7 | chrX | 155908315 | ||||||
| chrX:155908460
|
G | A | 2 | a0001c0001t0001g0012a0001c0001t0001g0074 | 3 | HG02109.hp2 HG03471.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.433+7873G>A | VAMP7 | ENSG00000124333.16 | transcript | ENST00000286448.12 | protein_coding | 5/7 | chrX | 155908460 | ||||||
| chrX:155908549
|
C | G | 3 | a0001c0002t0001g0026a0001c0002t0001g0027a0001c0002t0001g0028 | 3 | HG02630.hp2 HG02922.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.433+7962C>G | VAMP7 | ENSG00000124333.16 | transcript | ENST00000286448.12 | protein_coding | 5/7 | chrX | 155908549 | ||||||
| chrX:155908550
|
C | T | 1 | a0001c0001t0001g0035 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.433+7963C>T | VAMP7 | ENSG00000124333.16 | transcript | ENST00000286448.12 | protein_coding | 5/7 | chrX | 155908550 | ||||||
| chrX:155908565
|
A | AG | 1 | a0001c0001t0001g0147 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.433+7983dupG | VAMP7 | ENSG00000124333.16 | transcript | ENST00000286448.12 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chrX | 155908565 | |||||
| chrX:155908571
|
A | AG | 1 | a0001c0001t0001g0093 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.433+7989dupG | VAMP7 | ENSG00000124333.16 | transcript | ENST00000286448.12 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chrX | 155908571 | |||||
| chrX:155908615
|
C | CTTTG | 102 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(99): Show | 120 | HG00099.hp2 HG00408.hp1 HG00558.hp2 others(117): Show |
intron_variant | MODIFIER | c.433+8029_433+8032d others(6): Show |
VAMP7 | ENSG00000124333.16 | transcript | ENST00000286448.12 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chrX | 155908615 | |||||
| chrX:155908798
|
T | C | 2 | a0001c0001t0001g0053a0001c0001t0001g0117 | 2 | HG03239.hp2 HG03688.hp1 |
intron_variant | MODIFIER | c.433+8211T>C | VAMP7 | ENSG00000124333.16 | transcript | ENST00000286448.12 | protein_coding | 5/7 | chrX | 155908798 | ||||||
| chrX:155908843
|
A | AGT | 2 | a0001c0001t0001g0070a0001c0001t0001g0073 | 2 | HG01346.hp2 HG01978.hp2 |
intron_variant | MODIFIER | c.433+8258_433+8259d others(4): Show |
VAMP7 | ENSG00000124333.16 | transcript | ENST00000286448.12 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chrX | 155908843 | |||||
| chrX:155908919
|
A | C | 94 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(91): Show | 112 | HG00099.hp2 HG00408.hp1 HG00558.hp2 others(109): Show |
intron_variant | MODIFIER | c.433+8332A>C | VAMP7 | ENSG00000124333.16 | transcript | ENST00000286448.12 | protein_coding | 5/7 | chrX | 155908919 | ||||||
| chrX:155909122
|
C | T | 3 | a0001c0002t0001g0026a0001c0002t0001g0027a0001c0002t0001g0028 | 3 | HG02630.hp2 HG02922.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.433+8535C>T | VAMP7 | ENSG00000124333.16 | transcript | ENST00000286448.12 | protein_coding | 5/7 | chrX | 155909122 | ||||||
| chrX:155909205
|
A | G | 1 | a0001c0001t0001g0023 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.433+8618A>G | VAMP7 | ENSG00000124333.16 | transcript | ENST00000286448.12 | protein_coding | 5/7 | chrX | 155909205 | ||||||
| chrX:155909400
|
A | G | 4 | a0001c0001t0001g0002a0001c0001t0001g0060a0001c0001t0001g0062others(1): Show | 7 | HG01891.hp1 HG02109.hp1 HG02280.hp1 others(4): Show |
intron_variant | MODIFIER | c.433+8813A>G | VAMP7 | ENSG00000124333.16 | transcript | ENST00000286448.12 | protein_coding | 5/7 | chrX | 155909400 | ||||||
| chrX:155909410
|
T | A | 3 | a0001c0001t0001g0033a0001c0001t0001g0034a0001c0001t0001g0035 | 3 | HG02615.hp2 HG02630.hp1 HG02809.hp2 |
intron_variant | MODIFIER | c.433+8823T>A | VAMP7 | ENSG00000124333.16 | transcript | ENST00000286448.12 | protein_coding | 5/7 | chrX | 155909410 | ||||||
| chrX:155909426
|
A | T | 2 | a0001c0001t0001g0122a0001c0001t0001g0123 | 2 | HG02615.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.433+8839A>T | VAMP7 | ENSG00000124333.16 | transcript | ENST00000286448.12 | protein_coding | 5/7 | chrX | 155909426 | ||||||
| chrX:155909607
|
G | T | 1 | a0001c0001t0001g0102 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.433+9020G>T | VAMP7 | ENSG00000124333.16 | transcript | ENST00000286448.12 | protein_coding | 5/7 | chrX | 155909607 | ||||||
| chrX:155909633
|
T | C | 2 | a0001c0001t0001g0065a0001c0001t0001g0082 | 2 | NA18992.hp2 NA19072.hp1 |
intron_variant | MODIFIER | c.433+9046T>C | VAMP7 | ENSG00000124333.16 | transcript | ENST00000286448.12 | protein_coding | 5/7 | chrX | 155909633 | ||||||
| chrX:155909704
|
T | C | 1 | a0001c0001t0004g0020 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.433+9117T>C | VAMP7 | ENSG00000124333.16 | transcript | ENST00000286448.12 | protein_coding | 5/7 | chrX | 155909704 | ||||||
| chrX:155909918
|
G | C | 2 | a0001c0001t0001g0040a0001c0001t0001g0047 | 2 | HG02451.hp1 HG02896.hp1 |
intron_variant | MODIFIER | c.433+9331G>C | VAMP7 | ENSG00000124333.16 | transcript | ENST00000286448.12 | protein_coding | 5/7 | chrX | 155909918 | ||||||
| chrX:155910156
|
T | C | 1 | a0001c0001t0001g0060 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.433+9569T>C | VAMP7 | ENSG00000124333.16 | transcript | ENST00000286448.12 | protein_coding | 5/7 | chrX | 155910156 | ||||||
| chrX:155910369
|
A | G | 3 | a0001c0001t0001g0002a0001c0001t0001g0060a0001c0001t0001g0153 | 6 | HG02109.hp1 HG02280.hp1 HG02976.hp1 others(3): Show |
intron_variant | MODIFIER | c.434-9444A>G | VAMP7 | ENSG00000124333.16 | transcript | ENST00000286448.12 | protein_coding | 5/7 | chrX | 155910369 | ||||||
| chrX:155910436
|
C | T | 8 | a0001c0001t0001g0023a0001c0001t0001g0024a0001c0001t0001g0025others(5): Show | 8 | HG02622.hp2 HG02630.hp2 HG02723.hp2 others(5): Show |
intron_variant | MODIFIER | c.434-9377C>T | VAMP7 | ENSG00000124333.16 | transcript | ENST00000286448.12 | protein_coding | 5/7 | chrX | 155910436 | ||||||
| chrX:155910466
|
A | C | 1 | a0001c0001t0001g0008 | 2 | HG01168.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.434-9347A>C | VAMP7 | ENSG00000124333.16 | transcript | ENST00000286448.12 | protein_coding | 5/7 | chrX | 155910466 | ||||||
| chrX:155910475
|
A | G | 1 | a0001c0001t0001g0050 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.434-9338A>G | VAMP7 | ENSG00000124333.16 | transcript | ENST00000286448.12 | protein_coding | 5/7 | chrX | 155910475 | ||||||
| chrX:155910586
|
G | GT | 5 | a0001c0001t0001g0023a0001c0001t0001g0081a0001c0002t0001g0026others(2): Show | 5 | HG02630.hp2 HG02886.hp2 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.434-9213dupT | VAMP7 | ENSG00000124333.16 | transcript | ENST00000286448.12 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chrX | 155910586 | |||||
| chrX:155910586
|
GT | G | 7 | a0001c0001t0001g0033a0001c0001t0001g0034a0001c0001t0001g0035others(4): Show | 7 | HG02615.hp2 HG02630.hp1 HG02683.hp1 others(4): Show |
intron_variant | MODIFIER | c.434-9213delT | VAMP7 | ENSG00000124333.16 | transcript | ENST00000286448.12 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chrX | 155910586 | |||||
| chrX:155910637
|
T | C | 5 | a0001c0001t0001g0023a0001c0001t0001g0024a0001c0001t0001g0025others(2): Show | 5 | HG02622.hp2 HG02723.hp2 HG02886.hp2 others(2): Show |
intron_variant | MODIFIER | c.434-9176T>C | VAMP7 | ENSG00000124333.16 | transcript | ENST00000286448.12 | protein_coding | 5/7 | chrX | 155910637 | ||||||
| chrX:155910801
|
T | C | 17 | a0001c0001t0001g0001a0001c0001t0001g0043a0001c0001t0001g0081others(14): Show | 19 | HG00408.hp1 NA18941.hp2 NA18954.hp2 others(16): Show |
intron_variant | MODIFIER | c.434-9012T>C | VAMP7 | ENSG00000124333.16 | transcript | ENST00000286448.12 | protein_coding | 5/7 | chrX | 155910801 | ||||||
| chrX:155910909
|
T | G | 3 | a0001c0001t0001g0087a0001c0001t0001g0088a0001c0001t0001g0089 | 3 | NA18967.hp1 NA18989.hp2 NA18998.hp2 |
intron_variant | MODIFIER | c.434-8904T>G | VAMP7 | ENSG00000124333.16 | transcript | ENST00000286448.12 | protein_coding | 5/7 | chrX | 155910909 | ||||||
| chrX:155911442
|
G | T | 1 | a0001c0001t0001g0047 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.434-8371G>T | VAMP7 | ENSG00000124333.16 | transcript | ENST00000286448.12 | protein_coding | 5/7 | chrX | 155911442 | ||||||
| chrX:155911590
|
A | G | 1 | a0001c0001t0006g0018 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.434-8223A>G | VAMP7 | ENSG00000124333.16 | transcript | ENST00000286448.12 | protein_coding | 5/7 | chrX | 155911590 | ||||||
| chrX:155912016
|
G | C | 1 | a0001c0001t0001g0009 | 2 | HG02004.hp2 HG02293.hp2 |
intron_variant | MODIFIER | c.434-7797G>C | VAMP7 | ENSG00000124333.16 | transcript | ENST00000286448.12 | protein_coding | 5/7 | chrX | 155912016 | ||||||
| chrX:155912034
|
A | G | 3 | a0001c0002t0001g0026a0001c0002t0001g0027a0001c0002t0001g0028 | 3 | HG02630.hp2 HG02922.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.434-7779A>G | VAMP7 | ENSG00000124333.16 | transcript | ENST00000286448.12 | protein_coding | 5/7 | chrX | 155912034 | ||||||
| chrX:155912099
|
C | T | 1 | a0001c0001t0004g0020 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.434-7714C>T | VAMP7 | ENSG00000124333.16 | transcript | ENST00000286448.12 | protein_coding | 5/7 | chrX | 155912099 | ||||||
| chrX:155912321
|
T | C | 102 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(99): Show | 120 | HG00099.hp2 HG00408.hp1 HG00558.hp2 others(117): Show |
intron_variant | MODIFIER | c.434-7492T>C | VAMP7 | ENSG00000124333.16 | transcript | ENST00000286448.12 | protein_coding | 5/7 | chrX | 155912321 | ||||||
| chrX:155912526
|
A | G | 94 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(91): Show | 112 | HG00099.hp2 HG00408.hp1 HG00558.hp2 others(109): Show |
intron_variant | MODIFIER | c.434-7287A>G | VAMP7 | ENSG00000124333.16 | transcript | ENST00000286448.12 | protein_coding | 5/7 | chrX | 155912526 | ||||||
| chrX:155912659
|
C | T | 1 | a0001c0001t0001g0019 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.434-7154C>T | VAMP7 | ENSG00000124333.16 | transcript | ENST00000286448.12 | protein_coding | 5/7 | chrX | 155912659 | ||||||
| chrX:155912722
|
C | T | 102 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(99): Show | 120 | HG00099.hp2 HG00408.hp1 HG00558.hp2 others(117): Show |
intron_variant | MODIFIER | c.434-7091C>T | VAMP7 | ENSG00000124333.16 | transcript | ENST00000286448.12 | protein_coding | 5/7 | chrX | 155912722 | ||||||
| chrX:155912736
|
A | G | 102 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(99): Show | 120 | HG00099.hp2 HG00408.hp1 HG00558.hp2 others(117): Show |
intron_variant | MODIFIER | c.434-7077A>G | VAMP7 | ENSG00000124333.16 | transcript | ENST00000286448.12 | protein_coding | 5/7 | chrX | 155912736 | ||||||
| chrX:155912756
|
A | G | 12 | a0001c0001t0002g0003a0001c0001t0002g0006a0001c0001t0002g0017others(9): Show | 17 | HG00099.hp2 HG00639.hp1 HG01070.hp1 others(14): Show |
intron_variant | MODIFIER | c.434-7057A>G | VAMP7 | ENSG00000124333.16 | transcript | ENST00000286448.12 | protein_coding | 5/7 | chrX | 155912756 | ||||||
| chrX:155912813
|
A | G | 2 | a0001c0001t0001g0030a0001c0001t0001g0031 | 2 | HG03041.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.434-7000A>G | VAMP7 | ENSG00000124333.16 | transcript | ENST00000286448.12 | protein_coding | 5/7 | chrX | 155912813 | ||||||
| chrX:155912830
|
T | G | 1 | a0001c0001t0001g0065 | 1 | NA19072.hp1 | intron_variant | MODIFIER | c.434-6983T>G | VAMP7 | ENSG00000124333.16 | transcript | ENST00000286448.12 | protein_coding | 5/7 | chrX | 155912830 | ||||||
| chrX:155913058
|
G | A | 102 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(99): Show | 120 | HG00099.hp2 HG00408.hp1 HG00558.hp2 others(117): Show |
intron_variant | MODIFIER | c.434-6755G>A | VAMP7 | ENSG00000124333.16 | transcript | ENST00000286448.12 | protein_coding | 5/7 | chrX | 155913058 | ||||||
| chrX:155913139
|
T | C | 4 | a0001c0001t0001g0021a0001c0001t0001g0022a0001c0001t0001g0061others(1): Show | 4 | HG00741.hp2 HG02132.hp2 HG02818.hp1 others(1): Show |
intron_variant | MODIFIER | c.434-6674T>C | VAMP7 | ENSG00000124333.16 | transcript | ENST00000286448.12 | protein_coding | 5/7 | chrX | 155913139 | ||||||
| chrX:155913154
|
A | G | 102 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(99): Show | 120 | HG00099.hp2 HG00408.hp1 HG00558.hp2 others(117): Show |
intron_variant | MODIFIER | c.434-6659A>G | VAMP7 | ENSG00000124333.16 | transcript | ENST00000286448.12 | protein_coding | 5/7 | chrX | 155913154 | ||||||
| chrX:155913284
|
A | G | 1 | a0001c0001t0001g0019 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.434-6529A>G | VAMP7 | ENSG00000124333.16 | transcript | ENST00000286448.12 | protein_coding | 5/7 | chrX | 155913284 | ||||||
| chrX:155913420
|
TG | T | 1 | a0001c0001t0001g0152 | 1 | NA18992.hp1 | intron_variant | MODIFIER | c.434-6391delG | VAMP7 | ENSG00000124333.16 | transcript | ENST00000286448.12 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chrX | 155913420 | |||||
| chrX:155913461
|
GA | G | 1 | a0001c0001t0001g0152 | 1 | NA18992.hp1 | intron_variant | MODIFIER | c.434-6350delA | VAMP7 | ENSG00000124333.16 | transcript | ENST00000286448.12 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chrX | 155913461 | |||||
| chrX:155913514
|
T | TTTAA | 1 | a0001c0001t0002g0136 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.434-6298_434-6295d others(6): Show |
VAMP7 | ENSG00000124333.16 | transcript | ENST00000286448.12 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chrX | 155913514 | |||||
| chrX:155913609
|
A | G | 98 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(95): Show | 116 | HG00099.hp2 HG00408.hp1 HG00558.hp2 others(113): Show |
intron_variant | MODIFIER | c.434-6204A>G | VAMP7 | ENSG00000124333.16 | transcript | ENST00000286448.12 | protein_coding | 5/7 | chrX | 155913609 | ||||||
| chrX:155913644
|
G | T | 1 | a0001c0001t0001g0158 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.434-6169G>T | VAMP7 | ENSG00000124333.16 | transcript | ENST00000286448.12 | protein_coding | 5/7 | chrX | 155913644 | ||||||
| chrX:155913648
|
G | C | 1 | a0001c0001t0001g0158 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.434-6165G>C | VAMP7 | ENSG00000124333.16 | transcript | ENST00000286448.12 | protein_coding | 5/7 | chrX | 155913648 | ||||||
| chrX:155913852
|
G | A | 102 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(99): Show | 120 | HG00099.hp2 HG00408.hp1 HG00558.hp2 others(117): Show |
intron_variant | MODIFIER | c.434-5961G>A | VAMP7 | ENSG00000124333.16 | transcript | ENST00000286448.12 | protein_coding | 5/7 | chrX | 155913852 | ||||||
| chrX:155913891
|
GT | G | 1 | a0001c0001t0001g0152 | 1 | NA18992.hp1 | intron_variant | MODIFIER | c.434-5917delT | VAMP7 | ENSG00000124333.16 | transcript | ENST00000286448.12 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chrX | 155913891 | |||||
| chrX:155914082
|
C | T | 102 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(99): Show | 120 | HG00099.hp2 HG00408.hp1 HG00558.hp2 others(117): Show |
intron_variant | MODIFIER | c.434-5731C>T | VAMP7 | ENSG00000124333.16 | transcript | ENST00000286448.12 | protein_coding | 5/7 | chrX | 155914082 | ||||||
| chrX:155914159
|
G | T | 1 | a0001c0001t0006g0018 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.434-5654G>T | VAMP7 | ENSG00000124333.16 | transcript | ENST00000286448.12 | protein_coding | 5/7 | chrX | 155914159 | ||||||
| chrX:155914165
|
CT | C | 1 | a0001c0001t0001g0152 | 1 | NA18992.hp1 | intron_variant | MODIFIER | c.434-5644delT | VAMP7 | ENSG00000124333.16 | transcript | ENST00000286448.12 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chrX | 155914165 | |||||
| chrX:155914323
|
T | A | 1 | a0001c0001t0001g0047 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.434-5490T>A | VAMP7 | ENSG00000124333.16 | transcript | ENST00000286448.12 | protein_coding | 5/7 | chrX | 155914323 | ||||||
| chrX:155914451
|
G | T | 1 | a0001c0001t0001g0132 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.434-5362G>T | VAMP7 | ENSG00000124333.16 | transcript | ENST00000286448.12 | protein_coding | 5/7 | chrX | 155914451 | ||||||
| chrX:155914539
|
A | G | 1 | a0001c0001t0006g0018 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.434-5274A>G | VAMP7 | ENSG00000124333.16 | transcript | ENST00000286448.12 | protein_coding | 5/7 | chrX | 155914539 | ||||||
| chrX:155914667
|
T | C | 1 | a0001c0001t0001g0029 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.434-5146T>C | VAMP7 | ENSG00000124333.16 | transcript | ENST00000286448.12 | protein_coding | 5/7 | chrX | 155914667 | ||||||
| chrX:155914675
|
C | T | 1 | a0001c0001t0001g0043 | 1 | NA19089.hp1 | intron_variant | MODIFIER | c.434-5138C>T | VAMP7 | ENSG00000124333.16 | transcript | ENST00000286448.12 | protein_coding | 5/7 | chrX | 155914675 | ||||||
| chrX:155914758
|
A | G | 102 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(99): Show | 120 | HG00099.hp2 HG00408.hp1 HG00558.hp2 others(117): Show |
intron_variant | MODIFIER | c.434-5055A>G | VAMP7 | ENSG00000124333.16 | transcript | ENST00000286448.12 | protein_coding | 5/7 | chrX | 155914758 | ||||||
| chrX:155914828
|
T | G | 1 | a0001c0001t0001g0008 | 2 | HG01168.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.434-4985T>G | VAMP7 | ENSG00000124333.16 | transcript | ENST00000286448.12 | protein_coding | 5/7 | chrX | 155914828 | ||||||
| chrX:155914831
|
G | T | 1 | a0001c0001t0001g0019 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.434-4982G>T | VAMP7 | ENSG00000124333.16 | transcript | ENST00000286448.12 | protein_coding | 5/7 | chrX | 155914831 | ||||||
| chrX:155914947
|
C | T | 1 | a0001c0001t0006g0018 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.434-4866C>T | VAMP7 | ENSG00000124333.16 | transcript | ENST00000286448.12 | protein_coding | 5/7 | chrX | 155914947 | ||||||
| chrX:155915000
|
T | C | 7 | a0001c0001t0001g0019a0001c0001t0001g0023a0001c0001t0001g0158others(4): Show | 7 | HG01070.hp2 HG02622.hp2 HG02630.hp2 others(4): Show |
intron_variant | MODIFIER | c.434-4813T>C | VAMP7 | ENSG00000124333.16 | transcript | ENST00000286448.12 | protein_coding | 5/7 | chrX | 155915000 | ||||||
| chrX:155915256
|
C | T | 86 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0007others(83): Show | 101 | HG00099.hp2 HG00408.hp1 HG00558.hp2 others(98): Show |
intron_variant | MODIFIER | c.434-4557C>T | VAMP7 | ENSG00000124333.16 | transcript | ENST00000286448.12 | protein_coding | 5/7 | chrX | 155915256 | ||||||
| chrX:155915271
|
C | T | 7 | a0001c0001t0001g0014a0001c0001t0001g0015a0001c0001t0001g0016others(4): Show | 10 | HG02451.hp2 HG02809.hp1 HG02896.hp2 others(7): Show |
intron_variant | MODIFIER | c.434-4542C>T | VAMP7 | ENSG00000124333.16 | transcript | ENST00000286448.12 | protein_coding | 5/7 | chrX | 155915271 | ||||||
| chrX:155915298
|
C | G | 2 | a0001c0001t0001g0023a0001c0001t0001g0158 | 2 | HG02622.hp2 HG02886.hp2 |
intron_variant | MODIFIER | c.434-4515C>G | VAMP7 | ENSG00000124333.16 | transcript | ENST00000286448.12 | protein_coding | 5/7 | chrX | 155915298 | ||||||
| chrX:155915720
|
T | A | 1 | a0001c0001t0001g0066 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.434-4093T>A | VAMP7 | ENSG00000124333.16 | transcript | ENST00000286448.12 | protein_coding | 5/7 | chrX | 155915720 | ||||||
| chrX:155915765
|
G | A | 2 | a0001c0001t0001g0158a0001c0001t0004g0020 | 2 | HG02622.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.434-4048G>A | VAMP7 | ENSG00000124333.16 | transcript | ENST00000286448.12 | protein_coding | 5/7 | chrX | 155915765 | ||||||
| chrX:155916030
|
T | C | 1 | a0001c0001t0001g0023 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.434-3783T>C | VAMP7 | ENSG00000124333.16 | transcript | ENST00000286448.12 | protein_coding | 5/7 | chrX | 155916030 | ||||||
| chrX:155916031
|
G | A | 1 | a0001c0001t0001g0023 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.434-3782G>A | VAMP7 | ENSG00000124333.16 | transcript | ENST00000286448.12 | protein_coding | 5/7 | chrX | 155916031 | ||||||
| chrX:155916239
|
CTG | C | 6 | a0001c0001t0002g0006a0001c0001t0002g0133a0001c0001t0002g0134others(3): Show | 8 | HG00639.hp1 HG01257.hp2 HG01928.hp1 others(5): Show |
intron_variant | MODIFIER | c.434-3566_434-3565d others(4): Show |
VAMP7 | ENSG00000124333.16 | transcript | ENST00000286448.12 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chrX | 155916239 | |||||
| chrX:155916492
|
A | G | 99 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(96): Show | 117 | HG00099.hp2 HG00408.hp1 HG00558.hp2 others(114): Show |
intron_variant | MODIFIER | c.434-3321A>G | VAMP7 | ENSG00000124333.16 | transcript | ENST00000286448.12 | protein_coding | 5/7 | chrX | 155916492 | ||||||
| chrX:155916509
|
A | G | 1 | a0001c0001t0003g0116 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.434-3304A>G | VAMP7 | ENSG00000124333.16 | transcript | ENST00000286448.12 | protein_coding | 5/7 | chrX | 155916509 | ||||||
| chrX:155916713
|
G | A | 2 | a0001c0001t0001g0040a0001c0001t0001g0047 | 2 | HG02451.hp1 HG02896.hp1 |
intron_variant | MODIFIER | c.434-3100G>A | VAMP7 | ENSG00000124333.16 | transcript | ENST00000286448.12 | protein_coding | 5/7 | chrX | 155916713 | ||||||
| chrX:155916716
|
G | A | 1 | a0001c0001t0001g0011 | 2 | NA18953.hp2 NA19079.hp1 |
intron_variant | MODIFIER | c.434-3097G>A | VAMP7 | ENSG00000124333.16 | transcript | ENST00000286448.12 | protein_coding | 5/7 | chrX | 155916716 | ||||||
| chrX:155917026
|
C | T | 2 | a0001c0001t0001g0154a0001c0001t0001g0156 | 2 | HG01168.hp2 HG01517.hp1 |
intron_variant | MODIFIER | c.434-2787C>T | VAMP7 | ENSG00000124333.16 | transcript | ENST00000286448.12 | protein_coding | 5/7 | chrX | 155917026 | ||||||
| chrX:155917044
|
T | C | 1 | a0001c0001t0004g0020 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.434-2769T>C | VAMP7 | ENSG00000124333.16 | transcript | ENST00000286448.12 | protein_coding | 5/7 | chrX | 155917044 | ||||||
| chrX:155917112
|
A | G | 2 | a0001c0001t0001g0059a0001c0001t0006g0018 | 2 | HG00741.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.434-2701A>G | VAMP7 | ENSG00000124333.16 | transcript | ENST00000286448.12 | protein_coding | 5/7 | chrX | 155917112 | ||||||
| chrX:155917155
|
T | A | 3 | a0001c0002t0001g0026a0001c0002t0001g0027a0001c0002t0001g0028 | 3 | HG02630.hp2 HG02922.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.434-2658T>A | VAMP7 | ENSG00000124333.16 | transcript | ENST00000286448.12 | protein_coding | 5/7 | chrX | 155917155 | ||||||
| chrX:155917190
|
G | A | 1 | a0001c0001t0001g0019 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.434-2623G>A | VAMP7 | ENSG00000124333.16 | transcript | ENST00000286448.12 | protein_coding | 5/7 | chrX | 155917190 | ||||||
| chrX:155917272
|
G | T | 7 | a0001c0001t0001g0113a0001c0001t0001g0114a0001c0001t0001g0121others(4): Show | 7 | HG00408.hp2 HG00597.hp2 HG01168.hp2 others(4): Show |
intron_variant | MODIFIER | c.434-2541G>T | VAMP7 | ENSG00000124333.16 | transcript | ENST00000286448.12 | protein_coding | 5/7 | chrX | 155917272 | ||||||
| chrX:155917382
|
G | A | 18 | a0001c0001t0001g0001a0001c0001t0001g0023a0001c0001t0001g0043others(15): Show | 20 | HG00408.hp1 HG02886.hp2 NA18941.hp2 others(17): Show |
intron_variant | MODIFIER | c.434-2431G>A | VAMP7 | ENSG00000124333.16 | transcript | ENST00000286448.12 | protein_coding | 5/7 | chrX | 155917382 | ||||||
| chrX:155917438
|
C | T | 1 | a0001c0001t0001g0125 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.434-2375C>T | VAMP7 | ENSG00000124333.16 | transcript | ENST00000286448.12 | protein_coding | 5/7 | chrX | 155917438 | ||||||
| chrX:155917861
|
C | T | 3 | a0001c0001t0001g0044a0001c0001t0001g0058a0001c0001t0001g0059 | 3 | HG00741.hp1 HG01169.hp2 HG03239.hp1 |
intron_variant | MODIFIER | c.434-1952C>T | VAMP7 | ENSG00000124333.16 | transcript | ENST00000286448.12 | protein_coding | 5/7 | chrX | 155917861 | ||||||
| chrX:155918148
|
G | A | 1 | a0001c0001t0001g0023 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.434-1665G>A | VAMP7 | ENSG00000124333.16 | transcript | ENST00000286448.12 | protein_coding | 5/7 | chrX | 155918148 | ||||||
| chrX:155918149
|
C | T | 94 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(91): Show | 112 | HG00099.hp2 HG00408.hp1 HG00558.hp2 others(109): Show |
intron_variant | MODIFIER | c.434-1664C>T | VAMP7 | ENSG00000124333.16 | transcript | ENST00000286448.12 | protein_coding | 5/7 | chrX | 155918149 | ||||||
| chrX:155918247
|
G | A | 2 | a0001c0001t0001g0032a0001c0001t0001g0089 | 2 | HG04184.hp1 NA18989.hp2 |
intron_variant | MODIFIER | c.434-1566G>A | VAMP7 | ENSG00000124333.16 | transcript | ENST00000286448.12 | protein_coding | 5/7 | chrX | 155918247 | ||||||
| chrX:155918294
|
G | GC | 159 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(156): Show | 183 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(180): Show |
intron_variant | MODIFIER | c.434-1515dupC | VAMP7 | ENSG00000124333.16 | transcript | ENST00000286448.12 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chrX | 155918294 | |||||
| chrX:155918365
|
C | A | 1 | a0001c0001t0001g0019 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.434-1448C>A | VAMP7 | ENSG00000124333.16 | transcript | ENST00000286448.12 | protein_coding | 5/7 | chrX | 155918365 | ||||||
| chrX:155918366
|
T | A | 1 | a0001c0001t0001g0019 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.434-1447T>A | VAMP7 | ENSG00000124333.16 | transcript | ENST00000286448.12 | protein_coding | 5/7 | chrX | 155918366 | ||||||
| chrX:155918367
|
C | A | 1 | a0001c0001t0001g0019 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.434-1446C>A | VAMP7 | ENSG00000124333.16 | transcript | ENST00000286448.12 | protein_coding | 5/7 | chrX | 155918367 | ||||||
| chrX:155918441
|
G | A | 1 | a0001c0001t0001g0043 | 1 | NA19089.hp1 | intron_variant | MODIFIER | c.434-1372G>A | VAMP7 | ENSG00000124333.16 | transcript | ENST00000286448.12 | protein_coding | 5/7 | chrX | 155918441 | ||||||
| chrX:155918442
|
C | T | 1 | a0001c0001t0001g0019 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.434-1371C>T | VAMP7 | ENSG00000124333.16 | transcript | ENST00000286448.12 | protein_coding | 5/7 | chrX | 155918442 | ||||||
| chrX:155918512
|
C | T | 2 | a0001c0001t0001g0055a0001c0001t0001g0056 | 2 | HG01071.hp1 HG01081.hp1 |
intron_variant | MODIFIER | c.434-1301C>T | VAMP7 | ENSG00000124333.16 | transcript | ENST00000286448.12 | protein_coding | 5/7 | chrX | 155918512 | ||||||
| chrX:155918523
|
AC | A | 1 | a0001c0001t0004g0020 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.434-1289delC | VAMP7 | ENSG00000124333.16 | transcript | ENST00000286448.12 | protein_coding | 5/7 | chrX | 155918523 | ||||||
| chrX:155918599
|
C | T | 2 | a0001c0001t0001g0107a0001c0001t0001g0120 | 2 | HG00558.hp1 HG02523.hp1 |
intron_variant | MODIFIER | c.434-1214C>T | VAMP7 | ENSG00000124333.16 | transcript | ENST00000286448.12 | protein_coding | 5/7 | chrX | 155918599 | ||||||
| chrX:155918627
|
G | A | 1 | a0001c0001t0001g0019 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.434-1186G>A | VAMP7 | ENSG00000124333.16 | transcript | ENST00000286448.12 | protein_coding | 5/7 | chrX | 155918627 | ||||||
| chrX:155918738
|
G | T | 1 | a0001c0001t0001g0069 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.434-1075G>T | VAMP7 | ENSG00000124333.16 | transcript | ENST00000286448.12 | protein_coding | 5/7 | chrX | 155918738 | ||||||
| chrX:155918863
|
T | A | 1 | a0001c0001t0002g0135 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.434-950T>A | VAMP7 | ENSG00000124333.16 | transcript | ENST00000286448.12 | protein_coding | 5/7 | chrX | 155918863 | ||||||
| chrX:155918869
|
G | A | 2 | a0001c0001t0001g0076a0001c0001t0001g0080 | 2 | HG03540.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.434-944G>A | VAMP7 | ENSG00000124333.16 | transcript | ENST00000286448.12 | protein_coding | 5/7 | chrX | 155918869 | ||||||
| chrX:155918898
|
A | G | 2 | a0001c0001t0001g0122a0001c0001t0001g0123 | 2 | HG02615.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.434-915A>G | VAMP7 | ENSG00000124333.16 | transcript | ENST00000286448.12 | protein_coding | 5/7 | chrX | 155918898 | ||||||
| chrX:155918918
|
C | T | 1 | a0001c0001t0002g0135 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.434-895C>T | VAMP7 | ENSG00000124333.16 | transcript | ENST00000286448.12 | protein_coding | 5/7 | chrX | 155918918 | ||||||
| chrX:155918919
|
T | G | 1 | a0001c0001t0002g0135 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.434-894T>G | VAMP7 | ENSG00000124333.16 | transcript | ENST00000286448.12 | protein_coding | 5/7 | chrX | 155918919 | ||||||
| chrX:155919061
|
T | C | 1 | a0001c0001t0001g0103 | 1 | NA19080.hp1 | intron_variant | MODIFIER | c.434-752T>C | VAMP7 | ENSG00000124333.16 | transcript | ENST00000286448.12 | protein_coding | 5/7 | chrX | 155919061 | ||||||
| chrX:155919082
|
A | G | 2 | a0001c0001t0001g0030a0001c0001t0001g0031 | 2 | HG03041.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.434-731A>G | VAMP7 | ENSG00000124333.16 | transcript | ENST00000286448.12 | protein_coding | 5/7 | chrX | 155919082 | ||||||
| chrX:155919122
|
T | C | 1 | a0001c0001t0001g0045 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.434-691T>C | VAMP7 | ENSG00000124333.16 | transcript | ENST00000286448.12 | protein_coding | 5/7 | chrX | 155919122 | ||||||
| chrX:155919225
|
G | T | 4 | a0001c0001t0001g0021a0001c0001t0001g0022a0001c0001t0001g0061others(1): Show | 4 | HG00741.hp2 HG02132.hp2 HG02818.hp1 others(1): Show |
intron_variant | MODIFIER | c.434-588G>T | VAMP7 | ENSG00000124333.16 | transcript | ENST00000286448.12 | protein_coding | 5/7 | chrX | 155919225 | ||||||
| chrX:155919288
|
T | C | 101 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(98): Show | 119 | HG00099.hp2 HG00408.hp1 HG00558.hp2 others(116): Show |
intron_variant | MODIFIER | c.434-525T>C | VAMP7 | ENSG00000124333.16 | transcript | ENST00000286448.12 | protein_coding | 5/7 | chrX | 155919288 | ||||||
| chrX:155919290
|
G | T | 5 | a0001c0001t0001g0158a0001c0001t0004g0020a0001c0002t0001g0026others(2): Show | 5 | HG02622.hp2 HG02630.hp2 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.434-523G>T | VAMP7 | ENSG00000124333.16 | transcript | ENST00000286448.12 | protein_coding | 5/7 | chrX | 155919290 | ||||||
| chrX:155919395
|
A | AT | 1 | a0001c0001t0002g0135 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.434-417dupT | VAMP7 | ENSG00000124333.16 | transcript | ENST00000286448.12 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chrX | 155919395 | |||||
| chrX:155919414
|
T | G | 1 | a0001c0001t0001g0019 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.434-399T>G | VAMP7 | ENSG00000124333.16 | transcript | ENST00000286448.12 | protein_coding | 5/7 | chrX | 155919414 | ||||||
| chrX:155919427
|
T | TG | 1 | a0001c0001t0002g0135 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.434-386_434-385ins others(1): Show |
VAMP7 | ENSG00000124333.16 | transcript | ENST00000286448.12 | protein_coding | 5/7 | chrX | 155919427 | ||||||
| chrX:155919450
|
A | G | 3 | a0001c0001t0001g0002a0001c0001t0001g0060a0001c0001t0001g0153 | 6 | HG02109.hp1 HG02280.hp1 HG02976.hp1 others(3): Show |
intron_variant | MODIFIER | c.434-363A>G | VAMP7 | ENSG00000124333.16 | transcript | ENST00000286448.12 | protein_coding | 5/7 | chrX | 155919450 | ||||||
| chrX:155919526
|
G | A | 1 | a0001c0002t0001g0026 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.434-287G>A | VAMP7 | ENSG00000124333.16 | transcript | ENST00000286448.12 | protein_coding | 5/7 | chrX | 155919526 | ||||||
| chrX:155919698
|
C | T | 1 | a0001c0001t0001g0146 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.434-115C>T | VAMP7 | ENSG00000124333.16 | transcript | ENST00000286448.12 | protein_coding | 5/7 | chrX | 155919698 | ||||||
| chrX:155919982
|
G | GT | 3 | a0001c0001t0001g0019a0001c0001t0001g0023a0001c0001t0001g0106 | 3 | HG01070.hp2 HG01123.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.501+111dupT | VAMP7 | ENSG00000124333.16 | transcript | ENST00000286448.12 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chrX | 155919982 | |||||
| chrX:155920134
|
T | TA | 1 | a0001c0001t0002g0135 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.501+254_501+255ins others(1): Show |
VAMP7 | ENSG00000124333.16 | transcript | ENST00000286448.12 | protein_coding | 6/7 | chrX | 155920134 | ||||||
| chrX:155920332
|
C | T | 1 | a0001c0001t0001g0019 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.501+452C>T | VAMP7 | ENSG00000124333.16 | transcript | ENST00000286448.12 | protein_coding | 6/7 | chrX | 155920332 | ||||||
| chrX:155920356
|
A | G | 102 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(99): Show | 120 | HG00099.hp2 HG00408.hp1 HG00558.hp2 others(117): Show |
intron_variant | MODIFIER | c.501+476A>G | VAMP7 | ENSG00000124333.16 | transcript | ENST00000286448.12 | protein_coding | 6/7 | chrX | 155920356 | ||||||
| chrX:155920676
|
A | G | 86 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0007others(83): Show | 101 | HG00099.hp2 HG00408.hp1 HG00558.hp2 others(98): Show |
intron_variant | MODIFIER | c.501+796A>G | VAMP7 | ENSG00000124333.16 | transcript | ENST00000286448.12 | protein_coding | 6/7 | chrX | 155920676 | ||||||
| chrX:155920729
|
C | A | 94 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(91): Show | 112 | HG00099.hp2 HG00408.hp1 HG00558.hp2 others(109): Show |
intron_variant | MODIFIER | c.501+849C>A | VAMP7 | ENSG00000124333.16 | transcript | ENST00000286448.12 | protein_coding | 6/7 | chrX | 155920729 | ||||||
| chrX:155920775
|
G | A | 6 | a0001c0001t0001g0012a0001c0001t0001g0029a0001c0001t0001g0042others(3): Show | 7 | HG01884.hp2 HG02109.hp2 HG02622.hp1 others(4): Show |
intron_variant | MODIFIER | c.501+895G>A | VAMP7 | ENSG00000124333.16 | transcript | ENST00000286448.12 | protein_coding | 6/7 | chrX | 155920775 | ||||||
| chrX:155920785
|
C | T | 1 | a0001c0001t0001g0010 | 2 | NA18971.hp1 NA19011.hp1 |
intron_variant | MODIFIER | c.501+905C>T | VAMP7 | ENSG00000124333.16 | transcript | ENST00000286448.12 | protein_coding | 6/7 | chrX | 155920785 | ||||||
| chrX:155920833
|
T | TA | 1 | a0001c0001t0002g0135 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.501+955dupA | VAMP7 | ENSG00000124333.16 | transcript | ENST00000286448.12 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chrX | 155920833 | |||||
| chrX:155921153
|
T | C | 1 | a0001c0001t0001g0117 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.501+1273T>C | VAMP7 | ENSG00000124333.16 | transcript | ENST00000286448.12 | protein_coding | 6/7 | chrX | 155921153 | ||||||
| chrX:155921202
|
GA | G | 1 | a0001c0001t0002g0135 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.501+1326delA | VAMP7 | ENSG00000124333.16 | transcript | ENST00000286448.12 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chrX | 155921202 | |||||
| chrX:155921209
|
G | C | 1 | a0001c0001t0006g0018 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.501+1329G>C | VAMP7 | ENSG00000124333.16 | transcript | ENST00000286448.12 | protein_coding | 6/7 | chrX | 155921209 | ||||||
| chrX:155921268
|
A | C | 1 | a0001c0001t0002g0135 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.501+1388A>C | VAMP7 | ENSG00000124333.16 | transcript | ENST00000286448.12 | protein_coding | 6/7 | chrX | 155921268 | ||||||
| chrX:155921309
|
A | AT | 97 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(94): Show | 115 | HG00099.hp2 HG00408.hp1 HG00558.hp2 others(112): Show |
intron_variant | MODIFIER | c.501+1435dupT | VAMP7 | ENSG00000124333.16 | transcript | ENST00000286448.12 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chrX | 155921309 | |||||
| chrX:155921418
|
T | C | 1 | a0001c0001t0001g0050 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.501+1538T>C | VAMP7 | ENSG00000124333.16 | transcript | ENST00000286448.12 | protein_coding | 6/7 | chrX | 155921418 | ||||||
| chrX:155921422
|
C | T | 94 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(91): Show | 112 | HG00099.hp2 HG00408.hp1 HG00558.hp2 others(109): Show |
intron_variant | MODIFIER | c.501+1542C>T | VAMP7 | ENSG00000124333.16 | transcript | ENST00000286448.12 | protein_coding | 6/7 | chrX | 155921422 | ||||||
| chrX:155921970
|
AT | A | 1 | a0001c0001t0002g0135 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.501+2093delT | VAMP7 | ENSG00000124333.16 | transcript | ENST00000286448.12 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chrX | 155921970 | |||||
| chrX:155922109
|
T | G | 1 | a0001c0001t0002g0135 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.501+2229T>G | VAMP7 | ENSG00000124333.16 | transcript | ENST00000286448.12 | protein_coding | 6/7 | chrX | 155922109 | ||||||
| chrX:155922220
|
A | AT | 1 | a0001c0001t0002g0135 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.501+2344dupT | VAMP7 | ENSG00000124333.16 | transcript | ENST00000286448.12 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chrX | 155922220 | |||||
| chrX:155922244
|
GA | G | 1 | a0001c0001t0002g0135 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.501+2366delA | VAMP7 | ENSG00000124333.16 | transcript | ENST00000286448.12 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chrX | 155922244 | |||||
| chrX:155922563
|
AT | A | 1 | a0001c0001t0002g0135 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.501+2684delT | VAMP7 | ENSG00000124333.16 | transcript | ENST00000286448.12 | protein_coding | 6/7 | chrX | 155922563 | ||||||
| chrX:155922614
|
G | A | 1 | a0001c0001t0001g0158 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.501+2734G>A | VAMP7 | ENSG00000124333.16 | transcript | ENST00000286448.12 | protein_coding | 6/7 | chrX | 155922614 | ||||||
| chrX:155922677
|
GT | G | 1 | a0001c0001t0002g0135 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.501+2801delT | VAMP7 | ENSG00000124333.16 | transcript | ENST00000286448.12 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chrX | 155922677 | |||||
| chrX:155922776
|
T | C | 1 | a0001c0001t0001g0087 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.501+2896T>C | VAMP7 | ENSG00000124333.16 | transcript | ENST00000286448.12 | protein_coding | 6/7 | chrX | 155922776 | ||||||
| chrX:155922866
|
A | AT | 1 | a0001c0001t0002g0135 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.501+2989dupT | VAMP7 | ENSG00000124333.16 | transcript | ENST00000286448.12 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chrX | 155922866 | |||||
| chrX:155922975
|
C | T | 101 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(98): Show | 119 | HG00099.hp2 HG00408.hp1 HG00558.hp2 others(116): Show |
intron_variant | MODIFIER | c.501+3095C>T | VAMP7 | ENSG00000124333.16 | transcript | ENST00000286448.12 | protein_coding | 6/7 | chrX | 155922975 | ||||||
| chrX:155923000
|
T | C | 1 | a0001c0001t0006g0018 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.501+3120T>C | VAMP7 | ENSG00000124333.16 | transcript | ENST00000286448.12 | protein_coding | 6/7 | chrX | 155923000 | ||||||
| chrX:155923032
|
T | TA | 1 | a0001c0001t0002g0135 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.501+3155dupA | VAMP7 | ENSG00000124333.16 | transcript | ENST00000286448.12 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chrX | 155923032 | |||||
| chrX:155923285
|
G | A | 1 | a0001c0001t0001g0158 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.501+3405G>A | VAMP7 | ENSG00000124333.16 | transcript | ENST00000286448.12 | protein_coding | 6/7 | chrX | 155923285 | ||||||
| chrX:155923373
|
TG | T | 1 | a0001c0001t0002g0135 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.501+3495delG | VAMP7 | ENSG00000124333.16 | transcript | ENST00000286448.12 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chrX | 155923373 | |||||
| chrX:155923426
|
C | CT | 5 | a0001c0001t0001g0019a0001c0001t0006g0018a0001c0002t0001g0026others(2): Show | 5 | HG01070.hp2 HG02630.hp2 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.501+3557dupT | VAMP7 | ENSG00000124333.16 | transcript | ENST00000286448.12 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chrX | 155923426 | |||||
| chrX:155923426
|
CT | C | 1 | a0001c0001t0004g0020 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.501+3557delT | VAMP7 | ENSG00000124333.16 | transcript | ENST00000286448.12 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chrX | 155923426 | |||||
| chrX:155923440
|
A | C | 1 | a0001c0001t0001g0019 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.501+3560A>C | VAMP7 | ENSG00000124333.16 | transcript | ENST00000286448.12 | protein_coding | 6/7 | chrX | 155923440 | ||||||
| chrX:155923508
|
TG | T | 1 | a0001c0001t0002g0135 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.501+3630delG | VAMP7 | ENSG00000124333.16 | transcript | ENST00000286448.12 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chrX | 155923508 | |||||
| chrX:155923529
|
AT | A | 1 | a0001c0001t0002g0135 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.501+3651delT | VAMP7 | ENSG00000124333.16 | transcript | ENST00000286448.12 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chrX | 155923529 | |||||
| chrX:155923531
|
T | C | 3 | a0001c0002t0001g0026a0001c0002t0001g0027a0001c0002t0001g0028 | 3 | HG02630.hp2 HG02922.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.501+3651T>C | VAMP7 | ENSG00000124333.16 | transcript | ENST00000286448.12 | protein_coding | 6/7 | chrX | 155923531 | ||||||
| chrX:155923542
|
A | G | 1 | a0001c0001t0002g0135 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.501+3662A>G | VAMP7 | ENSG00000124333.16 | transcript | ENST00000286448.12 | protein_coding | 6/7 | chrX | 155923542 | ||||||
| chrX:155923612
|
CT | C | 1 | a0001c0001t0002g0135 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.501+3735delT | VAMP7 | ENSG00000124333.16 | transcript | ENST00000286448.12 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chrX | 155923612 | |||||
| chrX:155923620
|
T | C | 1 | a0001c0001t0006g0018 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.501+3740T>C | VAMP7 | ENSG00000124333.16 | transcript | ENST00000286448.12 | protein_coding | 6/7 | chrX | 155923620 | ||||||
| chrX:155923811
|
C | CT | 1 | a0001c0001t0002g0135 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.501+3937dupT | VAMP7 | ENSG00000124333.16 | transcript | ENST00000286448.12 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chrX | 155923811 | |||||
| chrX:155923944
|
CTTTTTT | C | 1 | a0001c0001t0001g0095 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.501+4065_501+4070d others(8): Show |
VAMP7 | ENSG00000124333.16 | transcript | ENST00000286448.12 | protein_coding | 6/7 | chrX | 155923944 | ||||||
| chrX:155923993
|
AC | A | 1 | a0001c0001t0002g0135 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.501+4115delC | VAMP7 | ENSG00000124333.16 | transcript | ENST00000286448.12 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chrX | 155923993 | |||||
| chrX:155924032
|
A | G | 1 | a0001c0001t0001g0062 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.501+4152A>G | VAMP7 | ENSG00000124333.16 | transcript | ENST00000286448.12 | protein_coding | 6/7 | chrX | 155924032 | ||||||
| chrX:155924132
|
G | A | 1 | a0001c0001t0001g0023 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.501+4252G>A | VAMP7 | ENSG00000124333.16 | transcript | ENST00000286448.12 | protein_coding | 6/7 | chrX | 155924132 | ||||||
| chrX:155924157
|
T | TA | 1 | a0001c0001t0002g0135 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.501+4277_501+4278i others(3): Show |
VAMP7 | ENSG00000124333.16 | transcript | ENST00000286448.12 | protein_coding | 6/7 | chrX | 155924157 | ||||||
| chrX:155924158
|
T | A | 95 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(92): Show | 113 | HG00099.hp2 HG00408.hp1 HG00558.hp2 others(110): Show |
intron_variant | MODIFIER | c.501+4278T>A | VAMP7 | ENSG00000124333.16 | transcript | ENST00000286448.12 | protein_coding | 6/7 | chrX | 155924158 | ||||||
| chrX:155924177
|
G | GT | 1 | a0001c0001t0004g0020 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.501+4303dupT | VAMP7 | ENSG00000124333.16 | transcript | ENST00000286448.12 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chrX | 155924177 | |||||
| chrX:155924284
|
A | T | 1 | a0001c0001t0002g0135 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.501+4404A>T | VAMP7 | ENSG00000124333.16 | transcript | ENST00000286448.12 | protein_coding | 6/7 | chrX | 155924284 | ||||||
| chrX:155924521
|
T | G | 1 | a0001c0001t0001g0072 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.501+4641T>G | VAMP7 | ENSG00000124333.16 | transcript | ENST00000286448.12 | protein_coding | 6/7 | chrX | 155924521 | ||||||
| chrX:155924597
|
T | TA | 1 | a0001c0001t0002g0135 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.501+4726dupA | VAMP7 | ENSG00000124333.16 | transcript | ENST00000286448.12 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chrX | 155924597 | |||||
| chrX:155924665
|
A | AC | 1 | a0001c0001t0002g0135 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.501+4787dupC | VAMP7 | ENSG00000124333.16 | transcript | ENST00000286448.12 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chrX | 155924665 | |||||
| chrX:155924693
|
C | CT | 1 | a0001c0001t0002g0135 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.501+4813_501+4814i others(3): Show |
VAMP7 | ENSG00000124333.16 | transcript | ENST00000286448.12 | protein_coding | 6/7 | chrX | 155924693 | ||||||
| chrX:155924853
|
A | G | 1 | a0001c0001t0001g0039 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.501+4973A>G | VAMP7 | ENSG00000124333.16 | transcript | ENST00000286448.12 | protein_coding | 6/7 | chrX | 155924853 | ||||||
| chrX:155924872
|
CA | C | 1 | a0001c0001t0002g0135 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.501+4995delA | VAMP7 | ENSG00000124333.16 | transcript | ENST00000286448.12 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chrX | 155924872 | |||||
| chrX:155925096
|
C | CCT | 1 | a0001c0001t0002g0135 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.501+5216_501+5217i others(4): Show |
VAMP7 | ENSG00000124333.16 | transcript | ENST00000286448.12 | protein_coding | 6/7 | chrX | 155925096 | ||||||
| chrX:155925097
|
T | A | 1 | a0001c0001t0002g0135 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.501+5217T>A | VAMP7 | ENSG00000124333.16 | transcript | ENST00000286448.12 | protein_coding | 6/7 | chrX | 155925097 | ||||||
| chrX:155925240
|
TG | T | 1 | a0001c0001t0002g0135 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.501+5362delG | VAMP7 | ENSG00000124333.16 | transcript | ENST00000286448.12 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chrX | 155925240 | |||||
| chrX:155925550
|
G | GT | 1 | a0001c0001t0002g0135 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.501+5674dupT | VAMP7 | ENSG00000124333.16 | transcript | ENST00000286448.12 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chrX | 155925550 | |||||
| chrX:155925556
|
T | TA | 1 | a0001c0001t0002g0135 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.501+5677dupA | VAMP7 | ENSG00000124333.16 | transcript | ENST00000286448.12 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chrX | 155925556 | |||||
| chrX:155925592
|
T | TC | 1 | a0001c0001t0002g0135 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.501+5712_501+5713i others(3): Show |
VAMP7 | ENSG00000124333.16 | transcript | ENST00000286448.12 | protein_coding | 6/7 | chrX | 155925592 | ||||||
| chrX:155925638
|
G | GC | 1 | a0001c0001t0002g0135 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.501+5759dupC | VAMP7 | ENSG00000124333.16 | transcript | ENST00000286448.12 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chrX | 155925638 | |||||
| chrX:155925655
|
C | T | 1 | a0001c0001t0002g0134 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.501+5775C>T | VAMP7 | ENSG00000124333.16 | transcript | ENST00000286448.12 | protein_coding | 6/7 | chrX | 155925655 | ||||||
| chrX:155925681
|
TTAGA | T | 1 | a0001c0001t0001g0023 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.501+5808_501+5811d others(6): Show |
VAMP7 | ENSG00000124333.16 | transcript | ENST00000286448.12 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chrX | 155925681 | |||||
| chrX:155925792
|
A | AG | 1 | a0001c0001t0002g0135 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.501+5913dupG | VAMP7 | ENSG00000124333.16 | transcript | ENST00000286448.12 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chrX | 155925792 | |||||
| chrX:155925804
|
A | C | 1 | a0001c0001t0002g0135 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.501+5924A>C | VAMP7 | ENSG00000124333.16 | transcript | ENST00000286448.12 | protein_coding | 6/7 | chrX | 155925804 | ||||||
| chrX:155925805
|
G | A | 1 | a0001c0001t0002g0135 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.501+5925G>A | VAMP7 | ENSG00000124333.16 | transcript | ENST00000286448.12 | protein_coding | 6/7 | chrX | 155925805 | ||||||
| chrX:155925807
|
T | G | 1 | a0001c0001t0002g0135 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.501+5927T>G | VAMP7 | ENSG00000124333.16 | transcript | ENST00000286448.12 | protein_coding | 6/7 | chrX | 155925807 | ||||||
| chrX:155925837
|
TC | T | 1 | a0001c0001t0002g0135 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.501+5960delC | VAMP7 | ENSG00000124333.16 | transcript | ENST00000286448.12 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chrX | 155925837 | |||||
| chrX:155925884
|
A | G | 1 | a0001c0001t0001g0033 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.501+6004A>G | VAMP7 | ENSG00000124333.16 | transcript | ENST00000286448.12 | protein_coding | 6/7 | chrX | 155925884 | ||||||
| chrX:155925888
|
AG | A | 1 | a0001c0001t0002g0135 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.501+6010delG | VAMP7 | ENSG00000124333.16 | transcript | ENST00000286448.12 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chrX | 155925888 | |||||
| chrX:155925897
|
A | AACG | 6 | a0001c0001t0001g0012a0001c0001t0001g0029a0001c0001t0001g0042others(3): Show | 7 | HG01884.hp2 HG02109.hp2 HG02622.hp1 others(4): Show |
intron_variant | MODIFIER | c.501+6020_501+6022d others(5): Show |
VAMP7 | ENSG00000124333.16 | transcript | ENST00000286448.12 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chrX | 155925897 | |||||
| chrX:155925900
|
G | A | 2 | a0001c0001t0001g0053a0001c0001t0001g0117 | 2 | HG03239.hp2 HG03688.hp1 |
intron_variant | MODIFIER | c.501+6020G>A | VAMP7 | ENSG00000124333.16 | transcript | ENST00000286448.12 | protein_coding | 6/7 | chrX | 155925900 | ||||||
| chrX:155925922
|
TC | T | 1 | a0001c0001t0002g0135 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.501+6044delC | VAMP7 | ENSG00000124333.16 | transcript | ENST00000286448.12 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chrX | 155925922 | |||||
| chrX:155925964
|
A | G | 1 | a0001c0001t0001g0023 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.501+6084A>G | VAMP7 | ENSG00000124333.16 | transcript | ENST00000286448.12 | protein_coding | 6/7 | chrX | 155925964 | ||||||
| chrX:155926137
|
T | C | 96 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(93): Show | 114 | HG00099.hp2 HG00408.hp1 HG00558.hp2 others(111): Show |
intron_variant | MODIFIER | c.501+6257T>C | VAMP7 | ENSG00000124333.16 | transcript | ENST00000286448.12 | protein_coding | 6/7 | chrX | 155926137 | ||||||
| chrX:155926199
|
C | T | 94 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(91): Show | 112 | HG00099.hp2 HG00408.hp1 HG00558.hp2 others(109): Show |
intron_variant | MODIFIER | c.501+6319C>T | VAMP7 | ENSG00000124333.16 | transcript | ENST00000286448.12 | protein_coding | 6/7 | chrX | 155926199 | ||||||
| chrX:155926399
|
T | C | 1 | a0001c0001t0001g0074 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.501+6519T>C | VAMP7 | ENSG00000124333.16 | transcript | ENST00000286448.12 | protein_coding | 6/7 | chrX | 155926399 | ||||||
| chrX:155926439
|
A | G | 3 | a0001c0002t0001g0026a0001c0002t0001g0027a0001c0002t0001g0028 | 3 | HG02630.hp2 HG02922.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.501+6559A>G | VAMP7 | ENSG00000124333.16 | transcript | ENST00000286448.12 | protein_coding | 6/7 | chrX | 155926439 | ||||||
| chrX:155926954
|
G | A | 1 | a0001c0001t0001g0096 | 1 | NA19055.hp1 | intron_variant | MODIFIER | c.501+7074G>A | VAMP7 | ENSG00000124333.16 | transcript | ENST00000286448.12 | protein_coding | 6/7 | chrX | 155926954 | ||||||
| chrX:155926967
|
C | T | 100 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(97): Show | 118 | HG00099.hp2 HG00408.hp1 HG00558.hp2 others(115): Show |
intron_variant | MODIFIER | c.501+7087C>T | VAMP7 | ENSG00000124333.16 | transcript | ENST00000286448.12 | protein_coding | 6/7 | chrX | 155926967 | ||||||
| chrX:155927008
|
A | G | 94 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(91): Show | 112 | HG00099.hp2 HG00408.hp1 HG00558.hp2 others(109): Show |
intron_variant | MODIFIER | c.501+7128A>G | VAMP7 | ENSG00000124333.16 | transcript | ENST00000286448.12 | protein_coding | 6/7 | chrX | 155927008 | ||||||
| chrX:155927177
|
A | T | 1 | a0001c0001t0001g0019 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.501+7297A>T | VAMP7 | ENSG00000124333.16 | transcript | ENST00000286448.12 | protein_coding | 6/7 | chrX | 155927177 | ||||||
| chrX:155927408
|
G | GA | 80 | a0001c0001t0001g0004a0001c0001t0001g0007a0001c0001t0001g0008others(77): Show | 93 | HG00099.hp2 HG00558.hp2 HG00597.hp1 others(90): Show |
intron_variant | MODIFIER | c.501+7540dupA | VAMP7 | ENSG00000124333.16 | transcript | ENST00000286448.12 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chrX | 155927408 | |||||
| chrX:155927408
|
G | GAA | 3 | a0001c0001t0001g0002a0001c0001t0001g0019a0001c0001t0001g0153 | 6 | HG01070.hp2 HG02109.hp1 HG02280.hp1 others(3): Show |
intron_variant | MODIFIER | c.501+7539_501+7540d others(4): Show |
VAMP7 | ENSG00000124333.16 | transcript | ENST00000286448.12 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chrX | 155927408 | |||||
| chrX:155927421
|
C | A | 2 | a0001c0001t0001g0076a0001c0001t0001g0158 | 2 | HG02622.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.501+7541C>A | VAMP7 | ENSG00000124333.16 | transcript | ENST00000286448.12 | protein_coding | 6/7 | chrX | 155927421 | ||||||
| chrX:155927453
|
A | G | 3 | a0001c0001t0002g0003a0001c0001t0002g0036a0001c0001t0002g0139 | 5 | HG01070.hp1 HG01071.hp2 HG01515.hp1 others(2): Show |
intron_variant | MODIFIER | c.501+7573A>G | VAMP7 | ENSG00000124333.16 | transcript | ENST00000286448.12 | protein_coding | 6/7 | chrX | 155927453 | ||||||
| chrX:155927481
|
C | CA | 13 | a0001c0001t0001g0023a0001c0001t0001g0032a0001c0001t0001g0053others(10): Show | 13 | HG00741.hp1 HG01123.hp1 HG01346.hp1 others(10): Show |
intron_variant | MODIFIER | c.501+7628dupA | VAMP7 | ENSG00000124333.16 | transcript | ENST00000286448.12 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chrX | 155927481 | |||||
| chrX:155927481
|
C | CAA | 2 | a0001c0001t0001g0118a0001c0001t0006g0018 | 2 | HG01361.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.501+7627_501+7628d others(4): Show |
VAMP7 | ENSG00000124333.16 | transcript | ENST00000286448.12 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chrX | 155927481 | |||||
| chrX:155927481
|
C | CAAA | 2 | a0001c0002t0001g0026a0001c0002t0001g0028 | 2 | HG02630.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.501+7626_501+7628d others(5): Show |
VAMP7 | ENSG00000124333.16 | transcript | ENST00000286448.12 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chrX | 155927481 | |||||
| chrX:155927481
|
C | CAAAA | 1 | a0001c0002t0001g0027 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.501+7625_501+7628d others(6): Show |
VAMP7 | ENSG00000124333.16 | transcript | ENST00000286448.12 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chrX | 155927481 | |||||
| chrX:155927481
|
CA | C | 5 | a0001c0001t0001g0030a0001c0001t0001g0031a0001c0001t0001g0033others(2): Show | 5 | HG01081.hp1 HG02615.hp2 HG02630.hp1 others(2): Show |
intron_variant | MODIFIER | c.501+7628delA | VAMP7 | ENSG00000124333.16 | transcript | ENST00000286448.12 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chrX | 155927481 | |||||
| chrX:155927481
|
CAAAA | C | 1 | a0001c0001t0001g0103 | 1 | NA19080.hp1 | intron_variant | MODIFIER | c.501+7625_501+7628d others(6): Show |
VAMP7 | ENSG00000124333.16 | transcript | ENST00000286448.12 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chrX | 155927481 | |||||
| chrX:155927481
|
CAAAAAAA others(4): Show |
C | 8 | a0001c0001t0001g0019a0001c0001t0001g0025a0001c0001t0001g0072others(5): Show | 8 | HG01070.hp2 HG02622.hp2 HG02723.hp2 others(5): Show |
intron_variant | MODIFIER | c.501+7618_501+7628d others(13): Show |
VAMP7 | ENSG00000124333.16 | transcript | ENST00000286448.12 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chrX | 155927481 | |||||
| chrX:155927481
|
CAAAAAAA others(5): Show |
C | 89 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(86): Show | 107 | HG00099.hp2 HG00408.hp1 HG00558.hp2 others(104): Show |
intron_variant | MODIFIER | c.501+7617_501+7628d others(14): Show |
VAMP7 | ENSG00000124333.16 | transcript | ENST00000286448.12 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chrX | 155927481 | |||||
| chrX:155927520
|
C | T | 3 | a0001c0001t0001g0009a0001c0001t0001g0070a0001c0001t0001g0073 | 4 | HG01346.hp2 HG01978.hp2 HG02004.hp2 others(1): Show |
intron_variant | MODIFIER | c.501+7640C>T | VAMP7 | ENSG00000124333.16 | transcript | ENST00000286448.12 | protein_coding | 6/7 | chrX | 155927520 | ||||||
| chrX:155927545
|
G | A | 159 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(156): Show | 183 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(180): Show |
intron_variant | MODIFIER | c.501+7665G>A | VAMP7 | ENSG00000124333.16 | transcript | ENST00000286448.12 | protein_coding | 6/7 | chrX | 155927545 | ||||||
| chrX:155927567
|
G | GT | 159 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(156): Show | 183 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(180): Show |
intron_variant | MODIFIER | c.501+7688dupT | VAMP7 | ENSG00000124333.16 | transcript | ENST00000286448.12 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chrX | 155927567 | |||||
| chrX:155927571
|
C | T | 159 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(156): Show | 183 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(180): Show |
intron_variant | MODIFIER | c.501+7691C>T | VAMP7 | ENSG00000124333.16 | transcript | ENST00000286448.12 | protein_coding | 6/7 | chrX | 155927571 | ||||||
| chrX:155927583
|
TC | T | 159 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(156): Show | 183 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(180): Show |
intron_variant | MODIFIER | c.501+7705delC | VAMP7 | ENSG00000124333.16 | transcript | ENST00000286448.12 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chrX | 155927583 | |||||
| chrX:155927765
|
G | GT | 43 | a0001c0001t0001g0004a0001c0001t0001g0009a0001c0001t0001g0010others(40): Show | 49 | HG00558.hp2 HG00597.hp1 HG00621.hp1 others(46): Show |
intron_variant | MODIFIER | c.501+7900dupT | VAMP7 | ENSG00000124333.16 | transcript | ENST00000286448.12 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chrX | 155927765 | |||||
| chrX:155927765
|
G | GTT | 54 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0007others(51): Show | 66 | HG00099.hp2 HG00408.hp1 HG00639.hp1 others(63): Show |
intron_variant | MODIFIER | c.501+7899_501+7900d others(4): Show |
VAMP7 | ENSG00000124333.16 | transcript | ENST00000286448.12 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chrX | 155927765 | |||||
| chrX:155927765
|
G | GTTT | 1 | a0001c0001t0001g0146 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.501+7898_501+7900d others(5): Show |
VAMP7 | ENSG00000124333.16 | transcript | ENST00000286448.12 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chrX | 155927765 | |||||
| chrX:155927772
|
T | G | 1 | a0001c0001t0001g0019 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.501+7892T>G | VAMP7 | ENSG00000124333.16 | transcript | ENST00000286448.12 | protein_coding | 6/7 | chrX | 155927772 | ||||||
| chrX:155927789
|
T | C | 1 | a0001c0001t0001g0019 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.501+7909T>C | VAMP7 | ENSG00000124333.16 | transcript | ENST00000286448.12 | protein_coding | 6/7 | chrX | 155927789 | ||||||
| chrX:155927829
|
T | C | 1 | a0001c0001t0001g0122 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.501+7949T>C | VAMP7 | ENSG00000124333.16 | transcript | ENST00000286448.12 | protein_coding | 6/7 | chrX | 155927829 | ||||||
| chrX:155927899
|
T | TTTG | 1 | a0001c0001t0001g0147 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.501+8040_501+8042d others(5): Show |
VAMP7 | ENSG00000124333.16 | transcript | ENST00000286448.12 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chrX | 155927899 | |||||
| chrX:155927899
|
TTTGTTG | T | 1 | a0001c0001t0001g0019 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.501+8037_501+8042d others(8): Show |
VAMP7 | ENSG00000124333.16 | transcript | ENST00000286448.12 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chrX | 155927899 | |||||
| chrX:155928279
|
T | C | 1 | a0001c0001t0001g0156 | 1 | HG01517.hp1 | intron_variant | MODIFIER | c.501+8399T>C | VAMP7 | ENSG00000124333.16 | transcript | ENST00000286448.12 | protein_coding | 6/7 | chrX | 155928279 | ||||||
| chrX:155928475
|
T | G | 1 | a0001c0001t0006g0018 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.501+8595T>G | VAMP7 | ENSG00000124333.16 | transcript | ENST00000286448.12 | protein_coding | 6/7 | chrX | 155928475 | ||||||
| chrX:155928534
|
G | T | 1 | a0001c0001t0001g0109 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.501+8654G>T | VAMP7 | ENSG00000124333.16 | transcript | ENST00000286448.12 | protein_coding | 6/7 | chrX | 155928534 | ||||||
| chrX:155928669
|
C | G | 94 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(91): Show | 112 | HG00099.hp2 HG00408.hp1 HG00558.hp2 others(109): Show |
intron_variant | MODIFIER | c.501+8789C>G | VAMP7 | ENSG00000124333.16 | transcript | ENST00000286448.12 | protein_coding | 6/7 | chrX | 155928669 | ||||||
| chrX:155928703
|
AC | A | 1 | a0001c0001t0001g0096 | 1 | NA19055.hp1 | intron_variant | MODIFIER | c.501+8824delC | VAMP7 | ENSG00000124333.16 | transcript | ENST00000286448.12 | protein_coding | 6/7 | chrX | 155928703 | ||||||
| chrX:155928826
|
A | G | 101 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(98): Show | 119 | HG00099.hp2 HG00408.hp1 HG00558.hp2 others(116): Show |
intron_variant | MODIFIER | c.501+8946A>G | VAMP7 | ENSG00000124333.16 | transcript | ENST00000286448.12 | protein_coding | 6/7 | chrX | 155928826 | ||||||
| chrX:155928867
|
G | A | 102 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(99): Show | 120 | HG00099.hp2 HG00408.hp1 HG00558.hp2 others(117): Show |
intron_variant | MODIFIER | c.501+8987G>A | VAMP7 | ENSG00000124333.16 | transcript | ENST00000286448.12 | protein_coding | 6/7 | chrX | 155928867 | ||||||
| chrX:155928957
|
C | A | 1 | a0001c0001t0001g0152 | 1 | NA18992.hp1 | intron_variant | MODIFIER | c.501+9077C>A | VAMP7 | ENSG00000124333.16 | transcript | ENST00000286448.12 | protein_coding | 6/7 | chrX | 155928957 | ||||||
| chrX:155929056
|
A | G | 1 | a0001c0001t0001g0023 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.501+9176A>G | VAMP7 | ENSG00000124333.16 | transcript | ENST00000286448.12 | protein_coding | 6/7 | chrX | 155929056 | ||||||
| chrX:155929173
|
A | T | 1 | a0001c0001t0001g0131 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.501+9293A>T | VAMP7 | ENSG00000124333.16 | transcript | ENST00000286448.12 | protein_coding | 6/7 | chrX | 155929173 | ||||||
| chrX:155929178
|
A | G | 1 | a0001c0001t0001g0117 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.501+9298A>G | VAMP7 | ENSG00000124333.16 | transcript | ENST00000286448.12 | protein_coding | 6/7 | chrX | 155929178 | ||||||
| chrX:155929215
|
C | T | 1 | a0001c0001t0001g0023 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.501+9335C>T | VAMP7 | ENSG00000124333.16 | transcript | ENST00000286448.12 | protein_coding | 6/7 | chrX | 155929215 | ||||||
| chrX:155929420
|
C | T | 1 | a0001c0001t0001g0038 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.501+9540C>T | VAMP7 | ENSG00000124333.16 | transcript | ENST00000286448.12 | protein_coding | 6/7 | chrX | 155929420 | ||||||
| chrX:155929450
|
C | A | 1 | a0001c0001t0001g0142 | 1 | NA19001.hp1 | intron_variant | MODIFIER | c.501+9570C>A | VAMP7 | ENSG00000124333.16 | transcript | ENST00000286448.12 | protein_coding | 6/7 | chrX | 155929450 | ||||||
| chrX:155929453
|
CT | C | 2 | a0001c0001t0001g0040a0001c0001t0001g0087 | 2 | HG02896.hp1 NA18967.hp1 |
intron_variant | MODIFIER | c.501+9574delT | VAMP7 | ENSG00000124333.16 | transcript | ENST00000286448.12 | protein_coding | 6/7 | chrX | 155929453 | ||||||
| chrX:155929529
|
C | T | 1 | a0001c0001t0001g0090 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.501+9649C>T | VAMP7 | ENSG00000124333.16 | transcript | ENST00000286448.12 | protein_coding | 6/7 | chrX | 155929529 | ||||||
| chrX:155929679
|
G | A | 3 | a0001c0001t0001g0119a0001c0001t0001g0122a0001c0001t0001g0123 | 3 | HG01891.hp2 HG02615.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.501+9799G>A | VAMP7 | ENSG00000124333.16 | transcript | ENST00000286448.12 | protein_coding | 6/7 | chrX | 155929679 | ||||||
| chrX:155929816
|
C | A | 4 | a0001c0001t0001g0002a0001c0001t0001g0060a0001c0001t0001g0062others(1): Show | 7 | HG01891.hp1 HG02109.hp1 HG02280.hp1 others(4): Show |
intron_variant | MODIFIER | c.502-9885C>A | VAMP7 | ENSG00000124333.16 | transcript | ENST00000286448.12 | protein_coding | 6/7 | chrX | 155929816 | ||||||
| chrX:155929905
|
G | C | 1 | a0001c0001t0006g0018 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.502-9796G>C | VAMP7 | ENSG00000124333.16 | transcript | ENST00000286448.12 | protein_coding | 6/7 | chrX | 155929905 | ||||||
| chrX:155930037
|
C | A | 1 | a0001c0001t0001g0130 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.502-9664C>A | VAMP7 | ENSG00000124333.16 | transcript | ENST00000286448.12 | protein_coding | 6/7 | chrX | 155930037 | ||||||
| chrX:155930039
|
A | G | 101 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(98): Show | 119 | HG00099.hp2 HG00408.hp1 HG00558.hp2 others(116): Show |
intron_variant | MODIFIER | c.502-9662A>G | VAMP7 | ENSG00000124333.16 | transcript | ENST00000286448.12 | protein_coding | 6/7 | chrX | 155930039 | ||||||
| chrX:155930082
|
C | T | 1 | a0001c0001t0001g0023 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.502-9619C>T | VAMP7 | ENSG00000124333.16 | transcript | ENST00000286448.12 | protein_coding | 6/7 | chrX | 155930082 | ||||||
| chrX:155930319
|
C | T | 3 | a0001c0002t0001g0026a0001c0002t0001g0027a0001c0002t0001g0028 | 3 | HG02630.hp2 HG02922.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.502-9382C>T | VAMP7 | ENSG00000124333.16 | transcript | ENST00000286448.12 | protein_coding | 6/7 | chrX | 155930319 | ||||||
| chrX:155930489
|
C | A | 1 | a0001c0001t0001g0127 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.502-9212C>A | VAMP7 | ENSG00000124333.16 | transcript | ENST00000286448.12 | protein_coding | 6/7 | chrX | 155930489 | ||||||
| chrX:155930489
|
C | CA | 9 | a0001c0001t0001g0044a0001c0001t0001g0050a0001c0001t0001g0052others(6): Show | 9 | HG00639.hp2 HG00741.hp1 HG01071.hp1 others(6): Show |
intron_variant | MODIFIER | c.502-9196dupA | VAMP7 | ENSG00000124333.16 | transcript | ENST00000286448.12 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chrX | 155930489 | |||||
| chrX:155930489
|
C | CAA | 2 | a0001c0001t0001g0058a0001c0001t0001g0144 | 2 | HG01346.hp1 HG03239.hp1 |
intron_variant | MODIFIER | c.502-9197_502-9196d others(4): Show |
VAMP7 | ENSG00000124333.16 | transcript | ENST00000286448.12 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chrX | 155930489 | |||||
| chrX:155930489
|
CA | C | 17 | a0001c0001t0001g0012a0001c0001t0001g0016a0001c0001t0001g0019others(14): Show | 19 | HG00597.hp1 HG01070.hp2 HG01884.hp2 others(16): Show |
intron_variant | MODIFIER | c.502-9196delA | VAMP7 | ENSG00000124333.16 | transcript | ENST00000286448.12 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chrX | 155930489 | |||||
| chrX:155930489
|
CAA | C | 89 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(86): Show | 106 | HG00099.hp2 HG00408.hp1 HG00558.hp2 others(103): Show |
intron_variant | MODIFIER | c.502-9197_502-9196d others(4): Show |
VAMP7 | ENSG00000124333.16 | transcript | ENST00000286448.12 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chrX | 155930489 | |||||
| chrX:155930493
|
A | C | 1 | a0001c0001t0001g0126 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.502-9208A>C | VAMP7 | ENSG00000124333.16 | transcript | ENST00000286448.12 | protein_coding | 6/7 | chrX | 155930493 | ||||||
| chrX:155930494
|
A | C | 8 | a0001c0001t0001g0012a0001c0001t0001g0029a0001c0001t0001g0042others(5): Show | 9 | HG00597.hp1 HG01884.hp2 HG02109.hp2 others(6): Show |
intron_variant | MODIFIER | c.502-9207A>C | VAMP7 | ENSG00000124333.16 | transcript | ENST00000286448.12 | protein_coding | 6/7 | chrX | 155930494 | ||||||
| chrX:155930495
|
A | C | 87 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(84): Show | 104 | HG00099.hp2 HG00408.hp1 HG00558.hp2 others(101): Show |
intron_variant | MODIFIER | c.502-9206A>C | VAMP7 | ENSG00000124333.16 | transcript | ENST00000286448.12 | protein_coding | 6/7 | chrX | 155930495 | ||||||
| chrX:155930509
|
G | A | 1 | a0001c0001t0004g0020 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.502-9192G>A | VAMP7 | ENSG00000124333.16 | transcript | ENST00000286448.12 | protein_coding | 6/7 | chrX | 155930509 | ||||||
| chrX:155930544
|
G | A | 1 | a0001c0001t0001g0143 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.502-9157G>A | VAMP7 | ENSG00000124333.16 | transcript | ENST00000286448.12 | protein_coding | 6/7 | chrX | 155930544 | ||||||
| chrX:155930651
|
C | CA | 1 | a0001c0001t0001g0106 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.502-9037dupA | VAMP7 | ENSG00000124333.16 | transcript | ENST00000286448.12 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chrX | 155930651 | |||||
| chrX:155930663
|
A | AG | 4 | a0001c0001t0006g0018a0001c0002t0001g0026a0001c0002t0001g0027others(1): Show | 4 | HG02630.hp2 HG02922.hp2 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.502-9038_502-9037i others(3): Show |
VAMP7 | ENSG00000124333.16 | transcript | ENST00000286448.12 | protein_coding | 6/7 | chrX | 155930663 | ||||||
| chrX:155930663
|
A | T | 1 | a0001c0001t0002g0138 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.502-9038A>T | VAMP7 | ENSG00000124333.16 | transcript | ENST00000286448.12 | protein_coding | 6/7 | chrX | 155930663 | ||||||
| chrX:155930664
|
A | AT | 3 | a0001c0001t0001g0099a0001c0001t0001g0100a0001c0001t0001g0102 | 3 | HG02257.hp1 HG02280.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.502-9029dupT | VAMP7 | ENSG00000124333.16 | transcript | ENST00000286448.12 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chrX | 155930664 | |||||
| chrX:155930664
|
A | T | 104 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(101): Show | 122 | HG00099.hp2 HG00408.hp1 HG00558.hp2 others(119): Show |
intron_variant | MODIFIER | c.502-9037A>T | VAMP7 | ENSG00000124333.16 | transcript | ENST00000286448.12 | protein_coding | 6/7 | chrX | 155930664 | ||||||
| chrX:155930694
|
TTA | T | 4 | a0001c0001t0006g0018a0001c0002t0001g0026a0001c0002t0001g0027others(1): Show | 4 | HG02630.hp2 HG02922.hp2 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.502-9005_502-9004d others(4): Show |
VAMP7 | ENSG00000124333.16 | transcript | ENST00000286448.12 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chrX | 155930694 | |||||
| chrX:155930719
|
T | A | 1 | a0001c0001t0001g0148 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.502-8982T>A | VAMP7 | ENSG00000124333.16 | transcript | ENST00000286448.12 | protein_coding | 6/7 | chrX | 155930719 | ||||||
| chrX:155930748
|
A | T | 1 | a0001c0001t0001g0052 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.502-8953A>T | VAMP7 | ENSG00000124333.16 | transcript | ENST00000286448.12 | protein_coding | 6/7 | chrX | 155930748 | ||||||
| chrX:155930786
|
G | A | 3 | a0001c0001t0001g0002a0001c0001t0001g0060a0001c0001t0001g0153 | 6 | HG02109.hp1 HG02280.hp1 HG02976.hp1 others(3): Show |
intron_variant | MODIFIER | c.502-8915G>A | VAMP7 | ENSG00000124333.16 | transcript | ENST00000286448.12 | protein_coding | 6/7 | chrX | 155930786 | ||||||
| chrX:155930857
|
C | T | 1 | a0001c0001t0001g0023 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.502-8844C>T | VAMP7 | ENSG00000124333.16 | transcript | ENST00000286448.12 | protein_coding | 6/7 | chrX | 155930857 | ||||||
| chrX:155930884
|
C | T | 1 | a0001c0001t0001g0023 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.502-8817C>T | VAMP7 | ENSG00000124333.16 | transcript | ENST00000286448.12 | protein_coding | 6/7 | chrX | 155930884 | ||||||
| chrX:155931044
|
C | A | 1 | a0001c0001t0001g0031 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.502-8657C>A | VAMP7 | ENSG00000124333.16 | transcript | ENST00000286448.12 | protein_coding | 6/7 | chrX | 155931044 | ||||||
| chrX:155931183
|
G | A | 1 | a0001c0001t0001g0037 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.502-8518G>A | VAMP7 | ENSG00000124333.16 | transcript | ENST00000286448.12 | protein_coding | 6/7 | chrX | 155931183 | ||||||
| chrX:155931416
|
G | A | 1 | a0001c0001t0001g0019 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.502-8285G>A | VAMP7 | ENSG00000124333.16 | transcript | ENST00000286448.12 | protein_coding | 6/7 | chrX | 155931416 | ||||||
| chrX:155931519
|
G | A | 1 | a0001c0001t0001g0057 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.502-8182G>A | VAMP7 | ENSG00000124333.16 | transcript | ENST00000286448.12 | protein_coding | 6/7 | chrX | 155931519 | ||||||
| chrX:155931617
|
T | C | 2 | a0001c0001t0001g0023a0001c0001t0006g0018 | 2 | HG02886.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.502-8084T>C | VAMP7 | ENSG00000124333.16 | transcript | ENST00000286448.12 | protein_coding | 6/7 | chrX | 155931617 | ||||||
| chrX:155931652
|
C | T | 159 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(156): Show | 183 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(180): Show |
intron_variant | MODIFIER | c.502-8049C>T | VAMP7 | ENSG00000124333.16 | transcript | ENST00000286448.12 | protein_coding | 6/7 | chrX | 155931652 | ||||||
| chrX:155931680
|
G | A | 1 | a0001c0001t0001g0152 | 1 | NA18992.hp1 | intron_variant | MODIFIER | c.502-8021G>A | VAMP7 | ENSG00000124333.16 | transcript | ENST00000286448.12 | protein_coding | 6/7 | chrX | 155931680 | ||||||
| chrX:155931822
|
A | G | 3 | a0001c0002t0001g0026a0001c0002t0001g0027a0001c0002t0001g0028 | 3 | HG02630.hp2 HG02922.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.502-7879A>G | VAMP7 | ENSG00000124333.16 | transcript | ENST00000286448.12 | protein_coding | 6/7 | chrX | 155931822 | ||||||
| chrX:155931828
|
T | G | 1 | a0001c0001t0001g0019 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.502-7873T>G | VAMP7 | ENSG00000124333.16 | transcript | ENST00000286448.12 | protein_coding | 6/7 | chrX | 155931828 | ||||||
| chrX:155931835
|
T | C | 1 | a0001c0001t0001g0143 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.502-7866T>C | VAMP7 | ENSG00000124333.16 | transcript | ENST00000286448.12 | protein_coding | 6/7 | chrX | 155931835 | ||||||
| chrX:155931876
|
A | AT | 1 | a0001c0001t0006g0018 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.502-7821dupT | VAMP7 | ENSG00000124333.16 | transcript | ENST00000286448.12 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chrX | 155931876 | |||||
| chrX:155931963
|
G | T | 96 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(93): Show | 114 | HG00099.hp2 HG00408.hp1 HG00558.hp2 others(111): Show |
intron_variant | MODIFIER | c.502-7738G>T | VAMP7 | ENSG00000124333.16 | transcript | ENST00000286448.12 | protein_coding | 6/7 | chrX | 155931963 | ||||||
| chrX:155931983
|
C | G | 1 | a0001c0001t0001g0019 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.502-7718C>G | VAMP7 | ENSG00000124333.16 | transcript | ENST00000286448.12 | protein_coding | 6/7 | chrX | 155931983 | ||||||
| chrX:155932057
|
A | C | 1 | a0001c0001t0001g0124 | 1 | NA18988.hp1 | intron_variant | MODIFIER | c.502-7644A>C | VAMP7 | ENSG00000124333.16 | transcript | ENST00000286448.12 | protein_coding | 6/7 | chrX | 155932057 | ||||||
| chrX:155932060
|
G | T | 1 | a0001c0001t0001g0023 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.502-7641G>T | VAMP7 | ENSG00000124333.16 | transcript | ENST00000286448.12 | protein_coding | 6/7 | chrX | 155932060 | ||||||
| chrX:155932272
|
G | A | 3 | a0001c0002t0001g0026a0001c0002t0001g0027a0001c0002t0001g0028 | 3 | HG02630.hp2 HG02922.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.502-7429G>A | VAMP7 | ENSG00000124333.16 | transcript | ENST00000286448.12 | protein_coding | 6/7 | chrX | 155932272 | ||||||
| chrX:155932351
|
T | G | 1 | a0001c0001t0002g0133 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.502-7350T>G | VAMP7 | ENSG00000124333.16 | transcript | ENST00000286448.12 | protein_coding | 6/7 | chrX | 155932351 | ||||||
| chrX:155932382
|
G | A | 1 | a0001c0001t0001g0019 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.502-7319G>A | VAMP7 | ENSG00000124333.16 | transcript | ENST00000286448.12 | protein_coding | 6/7 | chrX | 155932382 | ||||||
| chrX:155932468
|
C | G | 102 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(99): Show | 120 | HG00099.hp2 HG00408.hp1 HG00558.hp2 others(117): Show |
intron_variant | MODIFIER | c.502-7233C>G | VAMP7 | ENSG00000124333.16 | transcript | ENST00000286448.12 | protein_coding | 6/7 | chrX | 155932468 | ||||||
| chrX:155932517
|
A | G | 2 | a0001c0001t0001g0121a0001c0001t0001g0126 | 2 | HG00408.hp2 HG02293.hp1 |
intron_variant | MODIFIER | c.502-7184A>G | VAMP7 | ENSG00000124333.16 | transcript | ENST00000286448.12 | protein_coding | 6/7 | chrX | 155932517 | ||||||
| chrX:155932581
|
G | T | 1 | a0001c0001t0001g0060 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.502-7120G>T | VAMP7 | ENSG00000124333.16 | transcript | ENST00000286448.12 | protein_coding | 6/7 | chrX | 155932581 | ||||||
| chrX:155932958
|
G | A | 100 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(97): Show | 118 | HG00099.hp2 HG00408.hp1 HG00558.hp2 others(115): Show |
intron_variant | MODIFIER | c.502-6743G>A | VAMP7 | ENSG00000124333.16 | transcript | ENST00000286448.12 | protein_coding | 6/7 | chrX | 155932958 | ||||||
| chrX:155933129
|
G | A | 1 | a0001c0001t0001g0023 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.502-6572G>A | VAMP7 | ENSG00000124333.16 | transcript | ENST00000286448.12 | protein_coding | 6/7 | chrX | 155933129 | ||||||
| chrX:155933132
|
G | A | 1 | a0001c0001t0001g0158 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.502-6569G>A | VAMP7 | ENSG00000124333.16 | transcript | ENST00000286448.12 | protein_coding | 6/7 | chrX | 155933132 | ||||||
| chrX:155933139
|
A | C | 1 | a0001c0001t0006g0018 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.502-6562A>C | VAMP7 | ENSG00000124333.16 | transcript | ENST00000286448.12 | protein_coding | 6/7 | chrX | 155933139 | ||||||
| chrX:155933243
|
A | G | 1 | a0001c0001t0001g0055 | 1 | HG01071.hp1 | intron_variant | MODIFIER | c.502-6458A>G | VAMP7 | ENSG00000124333.16 | transcript | ENST00000286448.12 | protein_coding | 6/7 | chrX | 155933243 | ||||||
| chrX:155933253
|
G | A | 1 | a0001c0001t0001g0146 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.502-6448G>A | VAMP7 | ENSG00000124333.16 | transcript | ENST00000286448.12 | protein_coding | 6/7 | chrX | 155933253 | ||||||
| chrX:155933264
|
T | C | 1 | a0001c0001t0004g0020 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.502-6437T>C | VAMP7 | ENSG00000124333.16 | transcript | ENST00000286448.12 | protein_coding | 6/7 | chrX | 155933264 | ||||||
| chrX:155933356
|
TATTA | T | 1 | a0001c0001t0001g0104 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.502-6340_502-6337d others(6): Show |
VAMP7 | ENSG00000124333.16 | transcript | ENST00000286448.12 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chrX | 155933356 | |||||
| chrX:155933384
|
T | C | 2 | a0001c0001t0001g0158a0001c0001t0004g0020 | 2 | HG02622.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.502-6317T>C | VAMP7 | ENSG00000124333.16 | transcript | ENST00000286448.12 | protein_coding | 6/7 | chrX | 155933384 | ||||||
| chrX:155933395
|
T | C | 1 | a0001c0001t0001g0019 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.502-6306T>C | VAMP7 | ENSG00000124333.16 | transcript | ENST00000286448.12 | protein_coding | 6/7 | chrX | 155933395 | ||||||
| chrX:155933447
|
A | G | 1 | a0001c0001t0001g0061 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.502-6254A>G | VAMP7 | ENSG00000124333.16 | transcript | ENST00000286448.12 | protein_coding | 6/7 | chrX | 155933447 | ||||||
| chrX:155933524
|
G | C | 1 | a0001c0001t0006g0018 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.502-6177G>C | VAMP7 | ENSG00000124333.16 | transcript | ENST00000286448.12 | protein_coding | 6/7 | chrX | 155933524 | ||||||
| chrX:155933703
|
G | C | 1 | a0001c0001t0001g0043 | 1 | NA19089.hp1 | intron_variant | MODIFIER | c.502-5998G>C | VAMP7 | ENSG00000124333.16 | transcript | ENST00000286448.12 | protein_coding | 6/7 | chrX | 155933703 | ||||||
| chrX:155933713
|
G | A | 1 | a0001c0001t0006g0018 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.502-5988G>A | VAMP7 | ENSG00000124333.16 | transcript | ENST00000286448.12 | protein_coding | 6/7 | chrX | 155933713 | ||||||
| chrX:155933807
|
T | G | 2 | a0001c0001t0001g0076a0001c0001t0001g0080 | 2 | HG03540.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.502-5894T>G | VAMP7 | ENSG00000124333.16 | transcript | ENST00000286448.12 | protein_coding | 6/7 | chrX | 155933807 | ||||||
| chrX:155933821
|
C | T | 2 | a0001c0001t0001g0076a0001c0001t0001g0080 | 2 | HG03540.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.502-5880C>T | VAMP7 | ENSG00000124333.16 | transcript | ENST00000286448.12 | protein_coding | 6/7 | chrX | 155933821 | ||||||
| chrX:155933822
|
C | G | 2 | a0001c0001t0001g0076a0001c0001t0001g0080 | 2 | HG03540.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.502-5879C>G | VAMP7 | ENSG00000124333.16 | transcript | ENST00000286448.12 | protein_coding | 6/7 | chrX | 155933822 | ||||||
| chrX:155933824
|
T | C | 2 | a0001c0001t0001g0076a0001c0001t0001g0080 | 2 | HG03540.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.502-5877T>C | VAMP7 | ENSG00000124333.16 | transcript | ENST00000286448.12 | protein_coding | 6/7 | chrX | 155933824 | ||||||
| chrX:155933929
|
G | T | 1 | a0001c0001t0004g0020 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.502-5772G>T | VAMP7 | ENSG00000124333.16 | transcript | ENST00000286448.12 | protein_coding | 6/7 | chrX | 155933929 | ||||||
| chrX:155933995
|
T | C | 22 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0024others(19): Show | 29 | HG00099.hp2 HG00639.hp1 HG01070.hp1 others(26): Show |
intron_variant | MODIFIER | c.502-5706T>C | VAMP7 | ENSG00000124333.16 | transcript | ENST00000286448.12 | protein_coding | 6/7 | chrX | 155933995 | ||||||
| chrX:155934006
|
A | G | 5 | a0001c0001t0001g0019a0001c0001t0006g0018a0001c0002t0001g0026others(2): Show | 5 | HG01070.hp2 HG02630.hp2 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.502-5695A>G | VAMP7 | ENSG00000124333.16 | transcript | ENST00000286448.12 | protein_coding | 6/7 | chrX | 155934006 | ||||||
| chrX:155934153
|
G | A | 1 | a0001c0001t0001g0019 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.502-5548G>A | VAMP7 | ENSG00000124333.16 | transcript | ENST00000286448.12 | protein_coding | 6/7 | chrX | 155934153 | ||||||
| chrX:155934190
|
G | A | 1 | a0001c0001t0001g0110 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.502-5511G>A | VAMP7 | ENSG00000124333.16 | transcript | ENST00000286448.12 | protein_coding | 6/7 | chrX | 155934190 | ||||||
| chrX:155934299
|
G | C | 1 | a0001c0001t0001g0057 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.502-5402G>C | VAMP7 | ENSG00000124333.16 | transcript | ENST00000286448.12 | protein_coding | 6/7 | chrX | 155934299 | ||||||
| chrX:155934432
|
T | C | 2 | a0001c0001t0001g0096a0001c0001t0001g0097 | 2 | NA19010.hp2 NA19055.hp1 |
intron_variant | MODIFIER | c.502-5269T>C | VAMP7 | ENSG00000124333.16 | transcript | ENST00000286448.12 | protein_coding | 6/7 | chrX | 155934432 | ||||||
| chrX:155934723
|
G | A | 1 | a0001c0001t0001g0118 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.502-4978G>A | VAMP7 | ENSG00000124333.16 | transcript | ENST00000286448.12 | protein_coding | 6/7 | chrX | 155934723 | ||||||
| chrX:155934779
|
C | T | 94 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(91): Show | 112 | HG00099.hp2 HG00408.hp1 HG00558.hp2 others(109): Show |
intron_variant | MODIFIER | c.502-4922C>T | VAMP7 | ENSG00000124333.16 | transcript | ENST00000286448.12 | protein_coding | 6/7 | chrX | 155934779 | ||||||
| chrX:155934837
|
A | G | 100 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(97): Show | 118 | HG00099.hp2 HG00408.hp1 HG00558.hp2 others(115): Show |
intron_variant | MODIFIER | c.502-4864A>G | VAMP7 | ENSG00000124333.16 | transcript | ENST00000286448.12 | protein_coding | 6/7 | chrX | 155934837 | ||||||
| chrX:155934883
|
T | TA | 99 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(96): Show | 117 | HG00099.hp2 HG00408.hp1 HG00558.hp2 others(114): Show |
intron_variant | MODIFIER | c.502-4816dupA | VAMP7 | ENSG00000124333.16 | transcript | ENST00000286448.12 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chrX | 155934883 | |||||
| chrX:155935004
|
T | G | 1 | a0001c0001t0001g0033 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.502-4697T>G | VAMP7 | ENSG00000124333.16 | transcript | ENST00000286448.12 | protein_coding | 6/7 | chrX | 155935004 | ||||||
| chrX:155935061
|
G | A | 4 | a0001c0001t0001g0099a0001c0001t0001g0100a0001c0001t0001g0101others(1): Show | 4 | HG02257.hp1 HG02280.hp2 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.502-4640G>A | VAMP7 | ENSG00000124333.16 | transcript | ENST00000286448.12 | protein_coding | 6/7 | chrX | 155935061 | ||||||
| chrX:155935155
|
T | C | 1 | a0001c0001t0002g0138 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.502-4546T>C | VAMP7 | ENSG00000124333.16 | transcript | ENST00000286448.12 | protein_coding | 6/7 | chrX | 155935155 | ||||||
| chrX:155935633
|
G | A | 3 | a0001c0001t0001g0049a0001c0001t0001g0067a0001c0001t0001g0089 | 3 | HG00597.hp1 NA18989.hp2 NA19057.hp1 |
intron_variant | MODIFIER | c.502-4068G>A | VAMP7 | ENSG00000124333.16 | transcript | ENST00000286448.12 | protein_coding | 6/7 | chrX | 155935633 | ||||||
| chrX:155935698
|
A | G | 1 | a0001c0001t0006g0018 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.502-4003A>G | VAMP7 | ENSG00000124333.16 | transcript | ENST00000286448.12 | protein_coding | 6/7 | chrX | 155935698 | ||||||
| chrX:155935715
|
T | C | 1 | a0001c0001t0001g0054 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.502-3986T>C | VAMP7 | ENSG00000124333.16 | transcript | ENST00000286448.12 | protein_coding | 6/7 | chrX | 155935715 | ||||||
| chrX:155935774
|
G | A | 1 | a0001c0001t0001g0113 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.502-3927G>A | VAMP7 | ENSG00000124333.16 | transcript | ENST00000286448.12 | protein_coding | 6/7 | chrX | 155935774 | ||||||
| chrX:155936082
|
C | CG | 159 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(156): Show | 183 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(180): Show |
intron_variant | MODIFIER | c.502-3618dupG | VAMP7 | ENSG00000124333.16 | transcript | ENST00000286448.12 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chrX | 155936082 | |||||
| chrX:155936249
|
T | A | 1 | a0001c0001t0001g0019 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.502-3452T>A | VAMP7 | ENSG00000124333.16 | transcript | ENST00000286448.12 | protein_coding | 6/7 | chrX | 155936249 | ||||||
| chrX:155936445
|
A | G | 1 | a0001c0001t0001g0092 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.502-3256A>G | VAMP7 | ENSG00000124333.16 | transcript | ENST00000286448.12 | protein_coding | 6/7 | chrX | 155936445 | ||||||
| chrX:155936475
|
C | T | 4 | a0001c0001t0001g0049a0001c0001t0001g0067a0001c0001t0001g0079others(1): Show | 4 | HG00597.hp1 HG00621.hp1 NA18989.hp2 others(1): Show |
intron_variant | MODIFIER | c.502-3226C>T | VAMP7 | ENSG00000124333.16 | transcript | ENST00000286448.12 | protein_coding | 6/7 | chrX | 155936475 | ||||||
| chrX:155936493
|
T | C | 102 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(99): Show | 120 | HG00099.hp2 HG00408.hp1 HG00558.hp2 others(117): Show |
intron_variant | MODIFIER | c.502-3208T>C | VAMP7 | ENSG00000124333.16 | transcript | ENST00000286448.12 | protein_coding | 6/7 | chrX | 155936493 | ||||||
| chrX:155936527
|
T | G | 4 | a0001c0001t0001g0002a0001c0001t0001g0060a0001c0001t0001g0062others(1): Show | 7 | HG01891.hp1 HG02109.hp1 HG02280.hp1 others(4): Show |
intron_variant | MODIFIER | c.502-3174T>G | VAMP7 | ENSG00000124333.16 | transcript | ENST00000286448.12 | protein_coding | 6/7 | chrX | 155936527 | ||||||
| chrX:155936586
|
G | T | 1 | a0001c0001t0001g0061 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.502-3115G>T | VAMP7 | ENSG00000124333.16 | transcript | ENST00000286448.12 | protein_coding | 6/7 | chrX | 155936586 | ||||||
| chrX:155936652
|
G | A | 1 | a0001c0001t0001g0158 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.502-3049G>A | VAMP7 | ENSG00000124333.16 | transcript | ENST00000286448.12 | protein_coding | 6/7 | chrX | 155936652 | ||||||
| chrX:155936664
|
C | T | 1 | a0001c0001t0001g0152 | 1 | NA18992.hp1 | intron_variant | MODIFIER | c.502-3037C>T | VAMP7 | ENSG00000124333.16 | transcript | ENST00000286448.12 | protein_coding | 6/7 | chrX | 155936664 | ||||||
| chrX:155936676
|
G | T | 3 | a0001c0001t0001g0041a0001c0001t0001g0063a0001c0001t0001g0068 | 3 | HG02165.hp1 NA18977.hp1 NA19062.hp1 |
intron_variant | MODIFIER | c.502-3025G>T | VAMP7 | ENSG00000124333.16 | transcript | ENST00000286448.12 | protein_coding | 6/7 | chrX | 155936676 | ||||||
| chrX:155936731
|
G | A | 3 | a0001c0002t0001g0026a0001c0002t0001g0027a0001c0002t0001g0028 | 3 | HG02630.hp2 HG02922.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.502-2970G>A | VAMP7 | ENSG00000124333.16 | transcript | ENST00000286448.12 | protein_coding | 6/7 | chrX | 155936731 | ||||||
| chrX:155936771
|
G | A | 3 | a0001c0002t0001g0026a0001c0002t0001g0027a0001c0002t0001g0028 | 3 | HG02630.hp2 HG02922.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.502-2930G>A | VAMP7 | ENSG00000124333.16 | transcript | ENST00000286448.12 | protein_coding | 6/7 | chrX | 155936771 | ||||||
| chrX:155936779
|
C | T | 1 | a0001c0001t0004g0020 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.502-2922C>T | VAMP7 | ENSG00000124333.16 | transcript | ENST00000286448.12 | protein_coding | 6/7 | chrX | 155936779 | ||||||
| chrX:155937085
|
G | A | 1 | a0001c0001t0001g0117 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.502-2616G>A | VAMP7 | ENSG00000124333.16 | transcript | ENST00000286448.12 | protein_coding | 6/7 | chrX | 155937085 | ||||||
| chrX:155937494
|
G | C | 1 | a0001c0001t0004g0020 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.502-2207G>C | VAMP7 | ENSG00000124333.16 | transcript | ENST00000286448.12 | protein_coding | 6/7 | chrX | 155937494 | ||||||
| chrX:155938075
|
T | C | 2 | a0001c0001t0001g0030a0001c0001t0001g0031 | 2 | HG03041.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.502-1626T>C | VAMP7 | ENSG00000124333.16 | transcript | ENST00000286448.12 | protein_coding | 6/7 | chrX | 155938075 | ||||||
| chrX:155938281
|
C | T | 96 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(93): Show | 114 | HG00099.hp2 HG00408.hp1 HG00558.hp2 others(111): Show |
intron_variant | MODIFIER | c.502-1420C>T | VAMP7 | ENSG00000124333.16 | transcript | ENST00000286448.12 | protein_coding | 6/7 | chrX | 155938281 | ||||||
| chrX:155938296
|
G | A | 1 | a0001c0001t0001g0062 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.502-1405G>A | VAMP7 | ENSG00000124333.16 | transcript | ENST00000286448.12 | protein_coding | 6/7 | chrX | 155938296 | ||||||
| chrX:155938331
|
G | C | 6 | a0001c0001t0001g0019a0001c0001t0001g0023a0001c0001t0006g0018others(3): Show | 6 | HG01070.hp2 HG02630.hp2 HG02886.hp2 others(3): Show |
intron_variant | MODIFIER | c.502-1370G>C | VAMP7 | ENSG00000124333.16 | transcript | ENST00000286448.12 | protein_coding | 6/7 | chrX | 155938331 | ||||||
| chrX:155938377
|
C | T | 2 | a0001c0001t0001g0076a0001c0001t0001g0080 | 2 | HG03540.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.502-1324C>T | VAMP7 | ENSG00000124333.16 | transcript | ENST00000286448.12 | protein_coding | 6/7 | chrX | 155938377 | ||||||
| chrX:155938454
|
G | GT | 159 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(156): Show | 183 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(180): Show |
intron_variant | MODIFIER | c.502-1246dupT | VAMP7 | ENSG00000124333.16 | transcript | ENST00000286448.12 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chrX | 155938454 | |||||
| chrX:155938471
|
TA | T | 159 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(156): Show | 183 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(180): Show |
intron_variant | MODIFIER | c.502-1227delA | VAMP7 | ENSG00000124333.16 | transcript | ENST00000286448.12 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chrX | 155938471 | |||||
| chrX:155938668
|
G | A | 1 | a0001c0001t0001g0023 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.502-1033G>A | VAMP7 | ENSG00000124333.16 | transcript | ENST00000286448.12 | protein_coding | 6/7 | chrX | 155938668 | ||||||
| chrX:155938670
|
G | T | 1 | a0001c0001t0001g0002 | 4 | HG02109.hp1 HG02280.hp1 HG02976.hp1 others(1): Show |
intron_variant | MODIFIER | c.502-1031G>T | VAMP7 | ENSG00000124333.16 | transcript | ENST00000286448.12 | protein_coding | 6/7 | chrX | 155938670 | ||||||
| chrX:155938672
|
C | G | 1 | a0001c0001t0001g0143 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.502-1029C>G | VAMP7 | ENSG00000124333.16 | transcript | ENST00000286448.12 | protein_coding | 6/7 | chrX | 155938672 | ||||||
| chrX:155938873
|
AATG | A | 1 | a0001c0001t0001g0046 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.502-824_502-822del others(3): Show |
VAMP7 | ENSG00000124333.16 | transcript | ENST00000286448.12 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chrX | 155938873 | |||||
| chrX:155939060
|
T | C | 1 | a0001c0001t0006g0018 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.502-641T>C | VAMP7 | ENSG00000124333.16 | transcript | ENST00000286448.12 | protein_coding | 6/7 | chrX | 155939060 | ||||||
| chrX:155939075
|
T | TTG | 159 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(156): Show | 183 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(180): Show |
intron_variant | MODIFIER | c.502-625_502-624dup others(2): Show |
VAMP7 | ENSG00000124333.16 | transcript | ENST00000286448.12 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chrX | 155939075 | |||||
| chrX:155939087
|
G | GT | 159 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(156): Show | 183 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(180): Show |
intron_variant | MODIFIER | c.502-613dupT | VAMP7 | ENSG00000124333.16 | transcript | ENST00000286448.12 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chrX | 155939087 | |||||
| chrX:155939092
|
A | T | 159 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(156): Show | 183 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(180): Show |
intron_variant | MODIFIER | c.502-609A>T | VAMP7 | ENSG00000124333.16 | transcript | ENST00000286448.12 | protein_coding | 6/7 | chrX | 155939092 | ||||||
| chrX:155939093
|
C | A | 159 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(156): Show | 183 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(180): Show |
intron_variant | MODIFIER | c.502-608C>A | VAMP7 | ENSG00000124333.16 | transcript | ENST00000286448.12 | protein_coding | 6/7 | chrX | 155939093 | ||||||
| chrX:155939097
|
A | AC | 159 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(156): Show | 183 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(180): Show |
intron_variant | MODIFIER | c.502-602dupC | VAMP7 | ENSG00000124333.16 | transcript | ENST00000286448.12 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chrX | 155939097 | |||||
| chrX:155939106
|
G | GA | 159 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(156): Show | 183 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(180): Show |
intron_variant | MODIFIER | c.502-594dupA | VAMP7 | ENSG00000124333.16 | transcript | ENST00000286448.12 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chrX | 155939106 | |||||
| chrX:155939162
|
C | T | 1 | a0001c0001t0002g0133 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.502-539C>T | VAMP7 | ENSG00000124333.16 | transcript | ENST00000286448.12 | protein_coding | 6/7 | chrX | 155939162 | ||||||
| chrX:155939172
|
C | T | 1 | a0001c0001t0001g0023 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.502-529C>T | VAMP7 | ENSG00000124333.16 | transcript | ENST00000286448.12 | protein_coding | 6/7 | chrX | 155939172 | ||||||
| chrX:155939286
|
C | A | 1 | a0001c0001t0001g0019 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.502-415C>A | VAMP7 | ENSG00000124333.16 | transcript | ENST00000286448.12 | protein_coding | 6/7 | chrX | 155939286 | ||||||
| chrX:155939287
|
C | A | 1 | a0001c0001t0001g0019 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.502-414C>A | VAMP7 | ENSG00000124333.16 | transcript | ENST00000286448.12 | protein_coding | 6/7 | chrX | 155939287 | ||||||
| chrX:155939427
|
G | A | 1 | a0001c0001t0001g0146 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.502-274G>A | VAMP7 | ENSG00000124333.16 | transcript | ENST00000286448.12 | protein_coding | 6/7 | chrX | 155939427 | ||||||
| chrX:155939461
|
C | T | 1 | a0001c0001t0001g0053 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.502-240C>T | VAMP7 | ENSG00000124333.16 | transcript | ENST00000286448.12 | protein_coding | 6/7 | chrX | 155939461 | ||||||
| chrX:155939462
|
A | G | 5 | a0001c0001t0001g0019a0001c0001t0006g0018a0001c0002t0001g0026others(2): Show | 5 | HG01070.hp2 HG02630.hp2 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.502-239A>G | VAMP7 | ENSG00000124333.16 | transcript | ENST00000286448.12 | protein_coding | 6/7 | chrX | 155939462 | ||||||
| chrX:155939494
|
C | T | 86 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0007others(83): Show | 101 | HG00099.hp2 HG00408.hp1 HG00558.hp2 others(98): Show |
intron_variant | MODIFIER | c.502-207C>T | VAMP7 | ENSG00000124333.16 | transcript | ENST00000286448.12 | protein_coding | 6/7 | chrX | 155939494 | ||||||
| chrX:155939951
|
A | G | 1 | a0001c0001t0001g0015 | 2 | HG02451.hp2 HG02809.hp1 |
intron_variant | MODIFIER | c.594+158A>G | VAMP7 | ENSG00000124333.16 | transcript | ENST00000286448.12 | protein_coding | 7/7 | chrX | 155939951 | ||||||
| chrX:155939989
|
AATT | A | 5 | a0001c0001t0001g0030a0001c0001t0001g0031a0001c0001t0001g0033others(2): Show | 5 | HG02615.hp2 HG02630.hp1 HG02809.hp2 others(2): Show |
intron_variant | MODIFIER | c.594+202_594+204del others(3): Show |
VAMP7 | ENSG00000124333.16 | transcript | ENST00000286448.12 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chrX | 155939989 | |||||
| chrX:155940029
|
G | C | 1 | a0001c0001t0006g0018 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.594+236G>C | VAMP7 | ENSG00000124333.16 | transcript | ENST00000286448.12 | protein_coding | 7/7 | chrX | 155940029 | ||||||
| chrX:155940069
|
TG | T | 159 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(156): Show | 183 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(180): Show |
intron_variant | MODIFIER | c.594+278delG | VAMP7 | ENSG00000124333.16 | transcript | ENST00000286448.12 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chrX | 155940069 | |||||
| chrX:155940583
|
CA | C | 1 | a0001c0001t0001g0023 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.594+791delA | VAMP7 | ENSG00000124333.16 | transcript | ENST00000286448.12 | protein_coding | 7/7 | chrX | 155940583 | ||||||
| chrX:155940677
|
T | C | 1 | a0001c0001t0001g0038 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.594+884T>C | VAMP7 | ENSG00000124333.16 | transcript | ENST00000286448.12 | protein_coding | 7/7 | chrX | 155940677 | ||||||
| chrX:155941052
|
T | C | 94 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(91): Show | 112 | HG00099.hp2 HG00408.hp1 HG00558.hp2 others(109): Show |
intron_variant | MODIFIER | c.595-831T>C | VAMP7 | ENSG00000124333.16 | transcript | ENST00000286448.12 | protein_coding | 7/7 | chrX | 155941052 | ||||||
| chrX:155941053
|
G | A | 6 | a0001c0001t0001g0014a0001c0001t0001g0015a0001c0001t0001g0016others(3): Show | 9 | HG02451.hp2 HG02809.hp1 HG02896.hp2 others(6): Show |
intron_variant | MODIFIER | c.595-830G>A | VAMP7 | ENSG00000124333.16 | transcript | ENST00000286448.12 | protein_coding | 7/7 | chrX | 155941053 | ||||||
| chrX:155941092
|
C | G | 1 | a0001c0001t0004g0020 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.595-791C>G | VAMP7 | ENSG00000124333.16 | transcript | ENST00000286448.12 | protein_coding | 7/7 | chrX | 155941092 | ||||||
| chrX:155941147
|
CAAAAATA | C | 3 | a0001c0001t0001g0002a0001c0001t0001g0023a0001c0001t0001g0153 | 6 | HG02109.hp1 HG02280.hp1 HG02886.hp2 others(3): Show |
intron_variant | MODIFIER | c.595-719_595-713del others(7): Show |
VAMP7 | ENSG00000124333.16 | transcript | ENST00000286448.12 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chrX | 155941147 | |||||
| chrX:155941171
|
TA | T | 1 | a0001c0001t0001g0100 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.595-708delA | VAMP7 | ENSG00000124333.16 | transcript | ENST00000286448.12 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chrX | 155941171 | |||||
| chrX:155941229
|
A | T | 4 | a0001c0001t0001g0148a0001c0001t0001g0149a0001c0001t0001g0151others(1): Show | 4 | HG00280.hp1 NA18992.hp1 NA18998.hp1 others(1): Show |
intron_variant | MODIFIER | c.595-654A>T | VAMP7 | ENSG00000124333.16 | transcript | ENST00000286448.12 | protein_coding | 7/7 | chrX | 155941229 | ||||||
| chrX:155941334
|
A | G | 1 | a0001c0001t0007g0091 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.595-549A>G | VAMP7 | ENSG00000124333.16 | transcript | ENST00000286448.12 | protein_coding | 7/7 | chrX | 155941334 | ||||||
| chrX:155941425
|
A | G | 94 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(91): Show | 112 | HG00099.hp2 HG00408.hp1 HG00558.hp2 others(109): Show |
intron_variant | MODIFIER | c.595-458A>G | VAMP7 | ENSG00000124333.16 | transcript | ENST00000286448.12 | protein_coding | 7/7 | chrX | 155941425 | ||||||
| chrX:155941869
|
C | G | 1 | a0001c0001t0006g0018 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.595-14C>G | VAMP7 | ENSG00000124333.16 | transcript | ENST00000286448.12 | protein_coding | 7/7 | chrX | 155941869 | ||||||
| chrX:155941873
|
G | C | 58 | a0001c0001t0001g0005a0001c0001t0001g0013a0001c0001t0001g0014others(55): Show | 64 | HG00099.hp1 HG00280.hp1 HG00408.hp2 others(61): Show |
intron_variant | MODIFIER | c.595-10G>C | VAMP7 | ENSG00000124333.16 | transcript | ENST00000286448.12 | protein_coding | 7/7 | chrX | 155941873 |