Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| 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 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 660 | 181 | 56 | 34 | 73 | 6 | 10 | VAMP7_chrX_155876345_155948769 | VAMP7 | ATGGC others(655): Show |
chrX | 155876345 | 155948769 | ||
| a0001c0002 | 0/0 | 660 | 3 | 3 | 0 | 0 | 0 | 0 | VAMP7_chrX_155876345_155948769 | VAMP7 | ATGGC others(655): Show |
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 | GGCGT others(2589): Show |
chrX | 155876345 | 155948769 |
| a0001c0001t0002 | 0/0 | 2594 | 17 | 1 | 10 | 2 | 3 | 1 | VAMP7_chrX_155876345_155948769 | VAMP7 | GGCGT others(2589): Show |
chrX | 155876345 | 155948769 |
| a0001c0001t0003 | 0/0 | 2594 | 1 | 1 | 0 | 0 | 0 | 0 | VAMP7_chrX_155876345_155948769 | VAMP7 | GGCGT others(2589): Show |
chrX | 155876345 | 155948769 |
| a0001c0001t0004 | 0/0 | 2594 | 1 | 1 | 0 | 0 | 0 | 0 | VAMP7_chrX_155876345_155948769 | VAMP7 | GGCGT others(2589): Show |
chrX | 155876345 | 155948769 |
| a0001c0001t0005 | 0/0 | 2594 | 1 | 0 | 0 | 1 | 0 | 0 | VAMP7_chrX_155876345_155948769 | VAMP7 | GGCGT others(2589): Show |
chrX | 155876345 | 155948769 |
| a0001c0001t0006 | 0/0 | 2594 | 1 | 1 | 0 | 0 | 0 | 0 | VAMP7_chrX_155876345_155948769 | VAMP7 | GGCGT others(2589): Show |
chrX | 155876345 | 155948769 |
| a0001c0001t0007 | 0/0 | 2594 | 1 | 0 | 0 | 1 | 0 | 0 | VAMP7_chrX_155876345_155948769 | VAMP7 | GGCGT others(2589): Show |
chrX | 155876345 | 155948769 |
| a0001c0002t0001 | 0/0 | 2594 | 3 | 3 | 0 | 0 | 0 | 0 | VAMP7_chrX_155876345_155948769 | VAMP7 | GGCGT others(2589): Show |
chrX | 155876345 | 155948769 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0002 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | VAMP7_chrX_155876345_155948769 | VAMP7 | chrX | 155876345 | 155948769 |
| a0001c0001t0001g0003 | 0/0 | 4 | 0 | 1 | 3 | 0 | 0 | VAMP7_chrX_155876345_155948769 | VAMP7 | chrX | 155876345 | 155948769 |
| a0001c0001t0001g0005 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | VAMP7_chrX_155876345_155948769 | VAMP7 | chrX | 155876345 | 155948769 |
| a0001c0001t0001g0006 | 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 | 0 | 0 | 2 | 0 | 0 | VAMP7_chrX_155876345_155948769 | VAMP7 | chrX | 155876345 | 155948769 |
| a0001c0001t0001g0013 | 0/0 | 2 | 2 | 0 | 0 | 0 | 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 | 0 | 0 | 1 | 1 | 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 |
| a0001c0001t0001g0017 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | VAMP7_chrX_155876345_155948769 | VAMP7 | chrX | 155876345 | 155948769 |
| a0001c0001t0001g0018 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | VAMP7_chrX_155876345_155948769 | VAMP7 | chrX | 155876345 | 155948769 |
| a0001c0001t0001g0020 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | VAMP7_chrX_155876345_155948769 | VAMP7 | chrX | 155876345 | 155948769 |
| a0001c0001t0001g0022 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VAMP7_chrX_155876345_155948769 | VAMP7 | chrX | 155876345 | 155948769 |
| a0001c0001t0001g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VAMP7_chrX_155876345_155948769 | VAMP7 | chrX | 155876345 | 155948769 |
| a0001c0001t0001g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VAMP7_chrX_155876345_155948769 | VAMP7 | chrX | 155876345 | 155948769 |
| a0001c0001t0001g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VAMP7_chrX_155876345_155948769 | VAMP7 | chrX | 155876345 | 155948769 |
| a0001c0001t0001g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VAMP7_chrX_155876345_155948769 | VAMP7 | chrX | 155876345 | 155948769 |
| a0001c0001t0001g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VAMP7_chrX_155876345_155948769 | VAMP7 | chrX | 155876345 | 155948769 |
| a0001c0001t0001g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | 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 | 0 | 0 | 0 | 0 | 1 | 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 |
| a0001c0001t0001g0036 | 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 | 1 | 0 | 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 | 1 | 0 | 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 | 1 | 0 | 0 | 0 | 0 | VAMP7_chrX_155876345_155948769 | VAMP7 | chrX | 155876345 | 155948769 |
| a0001c0001t0001g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VAMP7_chrX_155876345_155948769 | VAMP7 | chrX | 155876345 | 155948769 |
| a0001c0001t0001g0046 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VAMP7_chrX_155876345_155948769 | VAMP7 | chrX | 155876345 | 155948769 |
| a0001c0001t0001g0047 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | VAMP7_chrX_155876345_155948769 | VAMP7 | chrX | 155876345 | 155948769 |
| a0001c0001t0001g0048 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | VAMP7_chrX_155876345_155948769 | VAMP7 | chrX | 155876345 | 155948769 |
| a0001c0001t0001g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VAMP7_chrX_155876345_155948769 | VAMP7 | chrX | 155876345 | 155948769 |
| a0001c0001t0001g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VAMP7_chrX_155876345_155948769 | VAMP7 | chrX | 155876345 | 155948769 |
| a0001c0001t0001g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VAMP7_chrX_155876345_155948769 | VAMP7 | chrX | 155876345 | 155948769 |
| a0001c0001t0001g0052 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | VAMP7_chrX_155876345_155948769 | VAMP7 | chrX | 155876345 | 155948769 |
| a0001c0001t0001g0053 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VAMP7_chrX_155876345_155948769 | VAMP7 | chrX | 155876345 | 155948769 |
| a0001c0001t0001g0054 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | VAMP7_chrX_155876345_155948769 | VAMP7 | chrX | 155876345 | 155948769 |
| a0001c0001t0001g0055 | 0/0 | 1 | 1 | 0 | 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 | 1 | 0 | 0 | 0 | VAMP7_chrX_155876345_155948769 | VAMP7 | chrX | 155876345 | 155948769 |
| a0001c0001t0001g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VAMP7_chrX_155876345_155948769 | VAMP7 | chrX | 155876345 | 155948769 |
| a0001c0001t0001g0059 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | VAMP7_chrX_155876345_155948769 | VAMP7 | chrX | 155876345 | 155948769 |
| a0001c0001t0001g0060 | 0/0 | 1 | 0 | 1 | 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 | 1 | 0 | 0 | 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 | 1 | 0 | 0 | 0 | VAMP7_chrX_155876345_155948769 | VAMP7 | chrX | 155876345 | 155948769 |
| a0001c0001t0001g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VAMP7_chrX_155876345_155948769 | VAMP7 | chrX | 155876345 | 155948769 |
| a0001c0001t0001g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VAMP7_chrX_155876345_155948769 | VAMP7 | chrX | 155876345 | 155948769 |
| a0001c0001t0001g0072 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VAMP7_chrX_155876345_155948769 | VAMP7 | chrX | 155876345 | 155948769 |
| a0001c0001t0001g0073 | 0/0 | 1 | 1 | 0 | 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 | 0 | 0 | 1 | 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 | 1 | 0 | 0 | 0 | 0 | VAMP7_chrX_155876345_155948769 | VAMP7 | chrX | 155876345 | 155948769 |
| a0001c0001t0001g0080 | 0/0 | 1 | 0 | 0 | 1 | 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 | 1 | 0 | 0 | 0 | VAMP7_chrX_155876345_155948769 | VAMP7 | chrX | 155876345 | 155948769 |
| a0001c0001t0001g0086 | 0/0 | 1 | 0 | 0 | 1 | 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 |
| a0001c0001t0001g0091 | 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 | 1 | 0 | 0 | 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 | 0 | 0 | 1 | 0 | 0 | VAMP7_chrX_155876345_155948769 | VAMP7 | chrX | 155876345 | 155948769 |
| a0001c0001t0001g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VAMP7_chrX_155876345_155948769 | VAMP7 | chrX | 155876345 | 155948769 |
| a0001c0001t0001g0102 | 0/0 | 1 | 0 | 0 | 1 | 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 | 0 | 1 | 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 | 0 | 1 | 0 | 0 | VAMP7_chrX_155876345_155948769 | VAMP7 | chrX | 155876345 | 155948769 |
| a0001c0001t0001g0111 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | VAMP7_chrX_155876345_155948769 | VAMP7 | chrX | 155876345 | 155948769 |
| a0001c0001t0001g0113 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | VAMP7_chrX_155876345_155948769 | VAMP7 | chrX | 155876345 | 155948769 |
| a0001c0001t0001g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VAMP7_chrX_155876345_155948769 | VAMP7 | chrX | 155876345 | 155948769 |
| a0001c0001t0001g0115 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VAMP7_chrX_155876345_155948769 | VAMP7 | chrX | 155876345 | 155948769 |
| a0001c0001t0001g0116 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | VAMP7_chrX_155876345_155948769 | VAMP7 | chrX | 155876345 | 155948769 |
| a0001c0001t0001g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VAMP7_chrX_155876345_155948769 | VAMP7 | chrX | 155876345 | 155948769 |
| a0001c0001t0001g0118 | 0/0 | 1 | 0 | 0 | 1 | 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 | 1 | 0 | 0 | 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 | 0 | 1 | 0 | 0 | 0 | VAMP7_chrX_155876345_155948769 | VAMP7 | chrX | 155876345 | 155948769 |
| a0001c0001t0001g0123 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VAMP7_chrX_155876345_155948769 | VAMP7 | chrX | 155876345 | 155948769 |
| a0001c0001t0001g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VAMP7_chrX_155876345_155948769 | VAMP7 | chrX | 155876345 | 155948769 |
| a0001c0001t0001g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VAMP7_chrX_155876345_155948769 | VAMP7 | chrX | 155876345 | 155948769 |
| a0001c0001t0001g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VAMP7_chrX_155876345_155948769 | VAMP7 | chrX | 155876345 | 155948769 |
| a0001c0001t0001g0127 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VAMP7_chrX_155876345_155948769 | VAMP7 | chrX | 155876345 | 155948769 |
| a0001c0001t0001g0128 | 0/0 | 1 | 0 | 1 | 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 |
| a0001c0001t0001g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VAMP7_chrX_155876345_155948769 | VAMP7 | chrX | 155876345 | 155948769 |
| a0001c0001t0001g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VAMP7_chrX_155876345_155948769 | VAMP7 | chrX | 155876345 | 155948769 |
| a0001c0001t0001g0139 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | VAMP7_chrX_155876345_155948769 | VAMP7 | chrX | 155876345 | 155948769 |
| a0001c0001t0001g0140 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VAMP7_chrX_155876345_155948769 | VAMP7 | chrX | 155876345 | 155948769 |
| a0001c0001t0001g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VAMP7_chrX_155876345_155948769 | VAMP7 | chrX | 155876345 | 155948769 |
| a0001c0001t0001g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VAMP7_chrX_155876345_155948769 | VAMP7 | chrX | 155876345 | 155948769 |
| a0001c0001t0001g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VAMP7_chrX_155876345_155948769 | VAMP7 | chrX | 155876345 | 155948769 |
| a0001c0001t0001g0144 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | VAMP7_chrX_155876345_155948769 | VAMP7 | chrX | 155876345 | 155948769 |
| a0001c0001t0001g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VAMP7_chrX_155876345_155948769 | VAMP7 | chrX | 155876345 | 155948769 |
| a0001c0001t0001g0146 | 0/0 | 1 | 0 | 0 | 1 | 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 | 1 | 0 | 0 | VAMP7_chrX_155876345_155948769 | VAMP7 | chrX | 155876345 | 155948769 |
| a0001c0001t0001g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VAMP7_chrX_155876345_155948769 | VAMP7 | chrX | 155876345 | 155948769 |
| a0001c0001t0001g0150 | 0/0 | 1 | 0 | 1 | 0 | 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 | 0 | 1 | 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 | 1 | 0 | 0 | 0 | 0 | VAMP7_chrX_155876345_155948769 | VAMP7 | chrX | 155876345 | 155948769 |
| a0001c0001t0002g0001 | 0/0 | 4 | 1 | 2 | 0 | 1 | 0 | VAMP7_chrX_155876345_155948769 | VAMP7 | chrX | 155876345 | 155948769 |
| a0001c0001t0002g0004 | 0/0 | 4 | 0 | 4 | 0 | 0 | 0 | VAMP7_chrX_155876345_155948769 | VAMP7 | chrX | 155876345 | 155948769 |
| a0001c0001t0002g0019 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | VAMP7_chrX_155876345_155948769 | VAMP7 | chrX | 155876345 | 155948769 |
| a0001c0001t0002g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VAMP7_chrX_155876345_155948769 | VAMP7 | chrX | 155876345 | 155948769 |
| a0001c0001t0002g0131 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VAMP7_chrX_155876345_155948769 | VAMP7 | chrX | 155876345 | 155948769 |
| a0001c0001t0002g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VAMP7_chrX_155876345_155948769 | VAMP7 | chrX | 155876345 | 155948769 |
| a0001c0001t0002g0133 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VAMP7_chrX_155876345_155948769 | VAMP7 | chrX | 155876345 | 155948769 |
| a0001c0001t0002g0134 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | VAMP7_chrX_155876345_155948769 | VAMP7 | chrX | 155876345 | 155948769 |
| a0001c0001t0002g0135 | 0/0 | 1 | 0 | 0 | 0 | 1 | 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 |
| a0001c0001t0003g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VAMP7_chrX_155876345_155948769 | VAMP7 | chrX | 155876345 | 155948769 |
| a0001c0001t0004g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VAMP7_chrX_155876345_155948769 | VAMP7 | chrX | 155876345 | 155948769 |
| a0001c0001t0005g0002 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VAMP7_chrX_155876345_155948769 | VAMP7 | chrX | 155876345 | 155948769 |
| a0001c0001t0006g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VAMP7_chrX_155876345_155948769 | VAMP7 | chrX | 155876345 | 155948769 |
| a0001c0001t0007g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VAMP7_chrX_155876345_155948769 | VAMP7 | chrX | 155876345 | 155948769 |
| a0001c0002t0001g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VAMP7_chrX_155876345_155948769 | VAMP7 | chrX | 155876345 | 155948769 |
| a0001c0002t0001g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VAMP7_chrX_155876345_155948769 | VAMP7 | chrX | 155876345 | 155948769 |
| a0001c0002t0001g0031 | 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 | g0015 | EUR | GBR | VAMP7_chrX_155876345_155948769 | VAMP7 | chrX | 155876345 | 155948769 |
| HG00099 | hp2 | a0001 | c0001 | t0002 | g0019 | EUR | GBR | VAMP7_chrX_155876345_155948769 | VAMP7 | chrX | 155876345 | 155948769 |
| HG00280 | hp1 | a0001 | c0001 | t0001 | g0144 | EUR | FIN | VAMP7_chrX_155876345_155948769 | VAMP7 | chrX | 155876345 | 155948769 |
| HG00408 | hp1 | a0001 | c0001 | t0001 | g0093 | EAS | CHS | VAMP7_chrX_155876345_155948769 | VAMP7 | chrX | 155876345 | 155948769 |
| HG00408 | hp2 | a0001 | c0001 | t0001 | g0118 | EAS | CHS | VAMP7_chrX_155876345_155948769 | VAMP7 | chrX | 155876345 | 155948769 |
| HG00558 | hp1 | a0001 | c0001 | t0001 | g0104 | EAS | CHS | VAMP7_chrX_155876345_155948769 | VAMP7 | chrX | 155876345 | 155948769 |
| HG00558 | hp2 | a0001 | c0001 | t0001 | g0129 | 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 | g0110 | EAS | CHS | VAMP7_chrX_155876345_155948769 | VAMP7 | chrX | 155876345 | 155948769 |
| HG00621 | hp1 | a0001 | c0001 | t0001 | g0078 | EAS | CHS | VAMP7_chrX_155876345_155948769 | VAMP7 | chrX | 155876345 | 155948769 |
| HG00639 | hp1 | a0001 | c0001 | t0002 | g0004 | AMR | PUR | VAMP7_chrX_155876345_155948769 | VAMP7 | chrX | 155876345 | 155948769 |
| HG00639 | hp2 | a0001 | c0001 | t0001 | g0053 | AMR | PUR | VAMP7_chrX_155876345_155948769 | VAMP7 | chrX | 155876345 | 155948769 |
| HG00741 | hp1 | a0001 | c0001 | t0001 | g0060 | AMR | PUR | VAMP7_chrX_155876345_155948769 | VAMP7 | chrX | 155876345 | 155948769 |
| HG00741 | hp2 | a0001 | c0001 | t0001 | g0122 | AMR | PUR | VAMP7_chrX_155876345_155948769 | VAMP7 | chrX | 155876345 | 155948769 |
| HG01070 | hp1 | a0001 | c0001 | t0002 | g0001 | AMR | PUR | VAMP7_chrX_155876345_155948769 | VAMP7 | chrX | 155876345 | 155948769 |
| HG01070 | hp2 | a0001 | c0001 | t0001 | g0022 | AMR | PUR | VAMP7_chrX_155876345_155948769 | VAMP7 | chrX | 155876345 | 155948769 |
| HG01071 | hp1 | a0001 | c0001 | t0001 | g0056 | AMR | PUR | VAMP7_chrX_155876345_155948769 | VAMP7 | chrX | 155876345 | 155948769 |
| HG01071 | hp2 | a0001 | c0001 | t0002 | g0001 | AMR | PUR | VAMP7_chrX_155876345_155948769 | VAMP7 | chrX | 155876345 | 155948769 |
| HG01081 | hp1 | a0001 | c0001 | t0001 | g0057 | AMR | PUR | VAMP7_chrX_155876345_155948769 | VAMP7 | chrX | 155876345 | 155948769 |
| HG01081 | hp2 | a0001 | c0001 | t0001 | g0041 | 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 | g0150 | 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 | g0046 | AMR | PUR | VAMP7_chrX_155876345_155948769 | VAMP7 | chrX | 155876345 | 155948769 |
| HG01257 | hp1 | a0001 | c0001 | t0001 | g0003 | AMR | CLM | VAMP7_chrX_155876345_155948769 | VAMP7 | chrX | 155876345 | 155948769 |
| HG01257 | hp2 | a0001 | c0001 | t0002 | g0133 | AMR | CLM | VAMP7_chrX_155876345_155948769 | VAMP7 | chrX | 155876345 | 155948769 |
| HG01346 | hp1 | a0001 | c0001 | t0001 | g0140 | AMR | CLM | VAMP7_chrX_155876345_155948769 | VAMP7 | chrX | 155876345 | 155948769 |
| HG01346 | hp2 | a0001 | c0001 | t0001 | g0072 | AMR | CLM | VAMP7_chrX_155876345_155948769 | VAMP7 | chrX | 155876345 | 155948769 |
| HG01361 | hp1 | a0001 | c0001 | t0001 | g0115 | AMR | CLM | VAMP7_chrX_155876345_155948769 | VAMP7 | chrX | 155876345 | 155948769 |
| HG01361 | hp2 | a0001 | c0001 | t0001 | g0128 | AMR | CLM | VAMP7_chrX_155876345_155948769 | VAMP7 | chrX | 155876345 | 155948769 |
| HG01515 | hp1 | a0001 | c0001 | t0002 | g0135 | EUR | IBS | VAMP7_chrX_155876345_155948769 | VAMP7 | chrX | 155876345 | 155948769 |
| HG01517 | hp1 | a0001 | c0001 | t0001 | g0152 | EUR | IBS | VAMP7_chrX_155876345_155948769 | VAMP7 | chrX | 155876345 | 155948769 |
| HG01517 | hp2 | a0001 | c0001 | t0002 | g0001 | EUR | IBS | VAMP7_chrX_155876345_155948769 | VAMP7 | chrX | 155876345 | 155948769 |
| HG01884 | hp1 | a0001 | c0001 | t0001 | g0039 | AFR | ACB | VAMP7_chrX_155876345_155948769 | VAMP7 | chrX | 155876345 | 155948769 |
| HG01884 | hp2 | a0001 | c0001 | t0001 | g0044 | AFR | ACB | VAMP7_chrX_155876345_155948769 | VAMP7 | chrX | 155876345 | 155948769 |
| HG01891 | hp1 | a0001 | c0001 | t0001 | g0063 | AFR | ACB | VAMP7_chrX_155876345_155948769 | VAMP7 | chrX | 155876345 | 155948769 |
| HG01891 | hp2 | a0001 | c0001 | t0001 | g0114 | AFR | ACB | VAMP7_chrX_155876345_155948769 | VAMP7 | chrX | 155876345 | 155948769 |
| HG01928 | hp1 | a0001 | c0001 | t0002 | g0131 | AMR | PEL | VAMP7_chrX_155876345_155948769 | VAMP7 | chrX | 155876345 | 155948769 |
| HG01978 | hp1 | a0001 | c0001 | t0002 | g0136 | AMR | PEL | VAMP7_chrX_155876345_155948769 | VAMP7 | chrX | 155876345 | 155948769 |
| HG01978 | hp2 | a0001 | c0001 | t0001 | g0069 | AMR | PEL | VAMP7_chrX_155876345_155948769 | VAMP7 | chrX | 155876345 | 155948769 |
| HG01993 | hp1 | a0001 | c0001 | t0002 | g0004 | AMR | PEL | VAMP7_chrX_155876345_155948769 | VAMP7 | chrX | 155876345 | 155948769 |
| HG01993 | hp2 | a0001 | c0001 | t0001 | g0127 | AMR | PEL | VAMP7_chrX_155876345_155948769 | VAMP7 | chrX | 155876345 | 155948769 |
| HG02004 | hp1 | a0001 | c0001 | t0002 | g0004 | 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 | g0097 | EAS | KHV | VAMP7_chrX_155876345_155948769 | VAMP7 | chrX | 155876345 | 155948769 |
| HG02132 | hp2 | a0001 | c0001 | t0001 | g0024 | EAS | KHV | VAMP7_chrX_155876345_155948769 | VAMP7 | chrX | 155876345 | 155948769 |
| HG02148 | hp1 | a0001 | c0001 | t0001 | g0106 | AMR | PEL | VAMP7_chrX_155876345_155948769 | VAMP7 | chrX | 155876345 | 155948769 |
| HG02148 | hp2 | a0001 | c0001 | t0002 | g0004 | AMR | PEL | VAMP7_chrX_155876345_155948769 | VAMP7 | chrX | 155876345 | 155948769 |
| HG02155 | hp1 | a0001 | c0001 | t0001 | g0058 | EAS | CDX | VAMP7_chrX_155876345_155948769 | VAMP7 | chrX | 155876345 | 155948769 |
| HG02155 | hp2 | a0001 | c0001 | t0002 | g0130 | EAS | CDX | VAMP7_chrX_155876345_155948769 | VAMP7 | chrX | 155876345 | 155948769 |
| HG02165 | hp1 | a0001 | c0001 | t0001 | g0043 | EAS | CDX | VAMP7_chrX_155876345_155948769 | VAMP7 | chrX | 155876345 | 155948769 |
| HG02165 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | CDX | VAMP7_chrX_155876345_155948769 | VAMP7 | chrX | 155876345 | 155948769 |
| HG02257 | hp1 | a0001 | c0001 | t0001 | g0099 | 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 | g0005 | AFR | ACB | VAMP7_chrX_155876345_155948769 | VAMP7 | chrX | 155876345 | 155948769 |
| HG02280 | hp2 | a0001 | c0001 | t0001 | g0014 | AFR | ACB | VAMP7_chrX_155876345_155948769 | VAMP7 | chrX | 155876345 | 155948769 |
| HG02293 | hp1 | a0001 | c0001 | t0001 | g0123 | 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 | g0019 | AMR | PEL | VAMP7_chrX_155876345_155948769 | VAMP7 | chrX | 155876345 | 155948769 |
| HG02451 | hp1 | a0001 | c0001 | t0001 | g0049 | AFR | ACB | VAMP7_chrX_155876345_155948769 | VAMP7 | chrX | 155876345 | 155948769 |
| HG02451 | hp2 | a0001 | c0001 | t0001 | g0017 | AFR | ACB | VAMP7_chrX_155876345_155948769 | VAMP7 | chrX | 155876345 | 155948769 |
| HG02523 | hp1 | a0001 | c0001 | t0001 | g0117 | EAS | KHV | VAMP7_chrX_155876345_155948769 | VAMP7 | chrX | 155876345 | 155948769 |
| HG02523 | hp2 | a0001 | c0001 | t0001 | g0151 | EAS | KHV | VAMP7_chrX_155876345_155948769 | VAMP7 | chrX | 155876345 | 155948769 |
| HG02615 | hp1 | a0001 | c0001 | t0001 | g0120 | AFR | GWD | VAMP7_chrX_155876345_155948769 | VAMP7 | chrX | 155876345 | 155948769 |
| HG02615 | hp2 | a0001 | c0001 | t0001 | g0038 | AFR | GWD | VAMP7_chrX_155876345_155948769 | VAMP7 | chrX | 155876345 | 155948769 |
| HG02622 | hp1 | a0001 | c0001 | t0001 | g0032 | AFR | GWD | VAMP7_chrX_155876345_155948769 | VAMP7 | chrX | 155876345 | 155948769 |
| HG02622 | hp2 | a0001 | c0001 | t0001 | g0154 | AFR | GWD | VAMP7_chrX_155876345_155948769 | VAMP7 | chrX | 155876345 | 155948769 |
| HG02630 | hp1 | a0001 | c0001 | t0001 | g0036 | AFR | GWD | VAMP7_chrX_155876345_155948769 | VAMP7 | chrX | 155876345 | 155948769 |
| HG02630 | hp2 | a0001 | c0002 | t0001 | g0029 | AFR | GWD | VAMP7_chrX_155876345_155948769 | VAMP7 | chrX | 155876345 | 155948769 |
| HG02683 | hp1 | a0001 | c0001 | t0002 | g0134 | SAS | PJL | VAMP7_chrX_155876345_155948769 | VAMP7 | chrX | 155876345 | 155948769 |
| HG02683 | hp2 | a0001 | c0001 | t0001 | g0111 | SAS | PJL | VAMP7_chrX_155876345_155948769 | VAMP7 | chrX | 155876345 | 155948769 |
| HG02723 | hp1 | a0001 | c0001 | t0002 | g0001 | AFR | GWD | VAMP7_chrX_155876345_155948769 | VAMP7 | chrX | 155876345 | 155948769 |
| HG02723 | hp2 | a0001 | c0001 | t0001 | g0028 | AFR | GWD | VAMP7_chrX_155876345_155948769 | VAMP7 | chrX | 155876345 | 155948769 |
| HG02809 | hp1 | a0001 | c0001 | t0001 | g0017 | AFR | GWD | VAMP7_chrX_155876345_155948769 | VAMP7 | chrX | 155876345 | 155948769 |
| HG02809 | hp2 | a0001 | c0001 | t0001 | g0037 | AFR | GWD | VAMP7_chrX_155876345_155948769 | VAMP7 | chrX | 155876345 | 155948769 |
| HG02818 | hp1 | a0001 | c0001 | t0001 | g0062 | AFR | GWD | VAMP7_chrX_155876345_155948769 | VAMP7 | chrX | 155876345 | 155948769 |
| HG02818 | hp2 | a0001 | c0001 | t0003 | g0112 | AFR | GWD | VAMP7_chrX_155876345_155948769 | VAMP7 | chrX | 155876345 | 155948769 |
| HG02886 | hp1 | a0001 | c0001 | t0001 | g0119 | AFR | GWD | VAMP7_chrX_155876345_155948769 | VAMP7 | chrX | 155876345 | 155948769 |
| HG02886 | hp2 | a0001 | c0001 | t0001 | g0026 | AFR | GWD | VAMP7_chrX_155876345_155948769 | VAMP7 | chrX | 155876345 | 155948769 |
| HG02896 | hp1 | a0001 | c0001 | t0001 | g0042 | AFR | GWD | VAMP7_chrX_155876345_155948769 | VAMP7 | chrX | 155876345 | 155948769 |
| HG02896 | hp2 | a0001 | c0001 | t0001 | g0018 | AFR | GWD | VAMP7_chrX_155876345_155948769 | VAMP7 | chrX | 155876345 | 155948769 |
| HG02897 | hp1 | a0001 | c0001 | t0001 | g0074 | AFR | GWD | VAMP7_chrX_155876345_155948769 | VAMP7 | chrX | 155876345 | 155948769 |
| HG02897 | hp2 | a0001 | c0001 | t0001 | g0018 | AFR | GWD | VAMP7_chrX_155876345_155948769 | VAMP7 | chrX | 155876345 | 155948769 |
| HG02922 | hp1 | a0001 | c0001 | t0001 | g0016 | AFR | ESN | VAMP7_chrX_155876345_155948769 | VAMP7 | chrX | 155876345 | 155948769 |
| HG02922 | hp2 | a0001 | c0002 | t0001 | g0031 | AFR | ESN | VAMP7_chrX_155876345_155948769 | VAMP7 | chrX | 155876345 | 155948769 |
| HG02970 | hp1 | a0001 | c0002 | t0001 | g0030 | AFR | ESN | VAMP7_chrX_155876345_155948769 | VAMP7 | chrX | 155876345 | 155948769 |
| HG02970 | hp2 | a0001 | c0001 | t0001 | g0014 | AFR | ESN | VAMP7_chrX_155876345_155948769 | VAMP7 | chrX | 155876345 | 155948769 |
| HG02976 | hp1 | a0001 | c0001 | t0001 | g0005 | AFR | ESN | VAMP7_chrX_155876345_155948769 | VAMP7 | chrX | 155876345 | 155948769 |
| HG02976 | hp2 | a0001 | c0001 | t0001 | g0040 | AFR | ESN | VAMP7_chrX_155876345_155948769 | VAMP7 | chrX | 155876345 | 155948769 |
| HG03041 | hp1 | a0001 | c0001 | t0001 | g0153 | AFR | GWD | VAMP7_chrX_155876345_155948769 | VAMP7 | chrX | 155876345 | 155948769 |
| HG03041 | hp2 | a0001 | c0001 | t0001 | g0035 | AFR | GWD | VAMP7_chrX_155876345_155948769 | VAMP7 | chrX | 155876345 | 155948769 |
| HG03195 | hp1 | a0001 | c0001 | t0004 | g0023 | AFR | ESN | VAMP7_chrX_155876345_155948769 | VAMP7 | chrX | 155876345 | 155948769 |
| HG03195 | hp2 | a0001 | c0001 | t0001 | g0149 | AFR | ESN | VAMP7_chrX_155876345_155948769 | VAMP7 | chrX | 155876345 | 155948769 |
| HG03239 | hp1 | a0001 | c0001 | t0001 | g0059 | SAS | PJL | VAMP7_chrX_155876345_155948769 | VAMP7 | chrX | 155876345 | 155948769 |
| HG03239 | hp2 | a0001 | c0001 | t0001 | g0113 | SAS | PJL | VAMP7_chrX_155876345_155948769 | VAMP7 | chrX | 155876345 | 155948769 |
| HG03453 | hp1 | a0001 | c0001 | t0001 | g0033 | AFR | MSL | VAMP7_chrX_155876345_155948769 | VAMP7 | chrX | 155876345 | 155948769 |
| HG03453 | hp2 | a0001 | c0001 | t0001 | g0125 | AFR | MSL | VAMP7_chrX_155876345_155948769 | VAMP7 | chrX | 155876345 | 155948769 |
| HG03486 | hp1 | a0001 | c0001 | t0006 | g0021 | AFR | MSL | VAMP7_chrX_155876345_155948769 | VAMP7 | chrX | 155876345 | 155948769 |
| HG03486 | hp2 | a0001 | c0001 | t0001 | g0027 | AFR | MSL | VAMP7_chrX_155876345_155948769 | VAMP7 | chrX | 155876345 | 155948769 |
| HG03491 | hp1 | a0001 | c0001 | t0001 | g0139 | SAS | PJL | VAMP7_chrX_155876345_155948769 | VAMP7 | chrX | 155876345 | 155948769 |
| HG03491 | hp2 | a0001 | c0001 | t0001 | g0048 | SAS | PJL | VAMP7_chrX_155876345_155948769 | VAMP7 | chrX | 155876345 | 155948769 |
| HG03516 | hp1 | a0001 | c0001 | t0001 | g0124 | AFR | ESN | VAMP7_chrX_155876345_155948769 | VAMP7 | chrX | 155876345 | 155948769 |
| HG03516 | hp2 | a0001 | c0001 | t0001 | g0141 | AFR | ESN | VAMP7_chrX_155876345_155948769 | VAMP7 | chrX | 155876345 | 155948769 |
| HG03540 | hp1 | a0001 | c0001 | t0001 | g0075 | AFR | GWD | VAMP7_chrX_155876345_155948769 | VAMP7 | chrX | 155876345 | 155948769 |
| HG03540 | hp2 | a0001 | c0001 | t0001 | g0016 | AFR | GWD | VAMP7_chrX_155876345_155948769 | VAMP7 | chrX | 155876345 | 155948769 |
| HG03688 | hp1 | a0001 | c0001 | t0001 | g0054 | SAS | STU | VAMP7_chrX_155876345_155948769 | VAMP7 | chrX | 155876345 | 155948769 |
| HG04184 | hp1 | a0001 | c0001 | t0001 | g0034 | SAS | BEB | VAMP7_chrX_155876345_155948769 | VAMP7 | chrX | 155876345 | 155948769 |
| HG04184 | hp2 | a0001 | c0001 | t0001 | g0047 | SAS | BEB | VAMP7_chrX_155876345_155948769 | VAMP7 | chrX | 155876345 | 155948769 |
| HG04199 | hp1 | a0001 | c0001 | t0001 | g0052 | SAS | STU | VAMP7_chrX_155876345_155948769 | VAMP7 | chrX | 155876345 | 155948769 |
| NA18612 | hp2 | a0001 | c0001 | t0001 | g0146 | EAS | CHB | VAMP7_chrX_155876345_155948769 | VAMP7 | chrX | 155876345 | 155948769 |
| NA18747 | hp1 | a0001 | c0001 | t0001 | g0068 | EAS | CHB | VAMP7_chrX_155876345_155948769 | VAMP7 | chrX | 155876345 | 155948769 |
| NA18940 | hp1 | a0001 | c0001 | t0001 | g0082 | EAS | JPT | VAMP7_chrX_155876345_155948769 | VAMP7 | chrX | 155876345 | 155948769 |
| NA18941 | hp1 | a0001 | c0001 | t0001 | g0015 | EAS | JPT | VAMP7_chrX_155876345_155948769 | VAMP7 | chrX | 155876345 | 155948769 |
| NA18941 | hp2 | a0001 | c0001 | t0001 | g0002 | 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 | g0012 | EAS | JPT | VAMP7_chrX_155876345_155948769 | VAMP7 | chrX | 155876345 | 155948769 |
| NA18954 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | VAMP7_chrX_155876345_155948769 | VAMP7 | chrX | 155876345 | 155948769 |
| NA18954 | hp2 | a0001 | c0001 | t0001 | g0126 | EAS | JPT | VAMP7_chrX_155876345_155948769 | VAMP7 | chrX | 155876345 | 155948769 |
| NA18959 | hp2 | a0001 | c0001 | t0001 | g0137 | EAS | JPT | VAMP7_chrX_155876345_155948769 | VAMP7 | chrX | 155876345 | 155948769 |
| NA18961 | hp1 | a0001 | c0001 | t0001 | g0109 | EAS | JPT | VAMP7_chrX_155876345_155948769 | VAMP7 | chrX | 155876345 | 155948769 |
| NA18965 | hp1 | a0001 | c0001 | t0005 | g0002 | EAS | JPT | VAMP7_chrX_155876345_155948769 | VAMP7 | chrX | 155876345 | 155948769 |
| NA18967 | hp1 | a0001 | c0001 | t0001 | g0086 | 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 | g0103 | EAS | JPT | VAMP7_chrX_155876345_155948769 | VAMP7 | chrX | 155876345 | 155948769 |
| NA18971 | hp1 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | VAMP7_chrX_155876345_155948769 | VAMP7 | chrX | 155876345 | 155948769 |
| NA18974 | hp2 | a0001 | c0001 | t0002 | g0132 | EAS | JPT | VAMP7_chrX_155876345_155948769 | VAMP7 | chrX | 155876345 | 155948769 |
| NA18977 | hp1 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | VAMP7_chrX_155876345_155948769 | VAMP7 | chrX | 155876345 | 155948769 |
| NA18980 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | VAMP7_chrX_155876345_155948769 | VAMP7 | chrX | 155876345 | 155948769 |
| NA18980 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | VAMP7_chrX_155876345_155948769 | VAMP7 | chrX | 155876345 | 155948769 |
| NA18981 | hp1 | a0001 | c0001 | t0001 | g0105 | EAS | JPT | VAMP7_chrX_155876345_155948769 | VAMP7 | chrX | 155876345 | 155948769 |
| NA18981 | hp2 | a0001 | c0001 | t0001 | g0050 | EAS | JPT | VAMP7_chrX_155876345_155948769 | VAMP7 | chrX | 155876345 | 155948769 |
| NA18985 | hp1 | a0001 | c0001 | t0001 | g0084 | EAS | JPT | VAMP7_chrX_155876345_155948769 | VAMP7 | chrX | 155876345 | 155948769 |
| NA18988 | hp1 | a0001 | c0001 | t0001 | g0121 | EAS | JPT | VAMP7_chrX_155876345_155948769 | VAMP7 | chrX | 155876345 | 155948769 |
| NA18989 | hp2 | a0001 | c0001 | t0001 | g0088 | 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 | g0148 | EAS | JPT | VAMP7_chrX_155876345_155948769 | VAMP7 | chrX | 155876345 | 155948769 |
| NA18992 | hp2 | a0001 | c0001 | t0001 | g0081 | EAS | JPT | VAMP7_chrX_155876345_155948769 | VAMP7 | chrX | 155876345 | 155948769 |
| NA18994 | hp1 | a0001 | c0001 | t0001 | g0083 | EAS | JPT | VAMP7_chrX_155876345_155948769 | VAMP7 | chrX | 155876345 | 155948769 |
| NA18995 | hp1 | a0001 | c0001 | t0001 | g0071 | EAS | JPT | VAMP7_chrX_155876345_155948769 | VAMP7 | chrX | 155876345 | 155948769 |
| NA18998 | hp1 | a0001 | c0001 | t0001 | g0147 | EAS | JPT | VAMP7_chrX_155876345_155948769 | VAMP7 | chrX | 155876345 | 155948769 |
| NA18998 | hp2 | a0001 | c0001 | t0001 | g0087 | EAS | JPT | VAMP7_chrX_155876345_155948769 | VAMP7 | chrX | 155876345 | 155948769 |
| NA19001 | hp1 | a0001 | c0001 | t0001 | g0138 | EAS | JPT | VAMP7_chrX_155876345_155948769 | VAMP7 | chrX | 155876345 | 155948769 |
| NA19001 | hp2 | a0001 | c0001 | t0001 | g0143 | EAS | JPT | VAMP7_chrX_155876345_155948769 | VAMP7 | chrX | 155876345 | 155948769 |
| NA19005 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | VAMP7_chrX_155876345_155948769 | VAMP7 | chrX | 155876345 | 155948769 |
| NA19009 | hp2 | a0001 | c0001 | t0001 | g0080 | EAS | JPT | VAMP7_chrX_155876345_155948769 | VAMP7 | chrX | 155876345 | 155948769 |
| NA19010 | hp1 | a0001 | c0001 | t0001 | g0077 | EAS | JPT | VAMP7_chrX_155876345_155948769 | VAMP7 | chrX | 155876345 | 155948769 |
| NA19010 | hp2 | a0001 | c0001 | t0001 | g0096 | EAS | JPT | VAMP7_chrX_155876345_155948769 | VAMP7 | chrX | 155876345 | 155948769 |
| NA19011 | hp1 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | VAMP7_chrX_155876345_155948769 | VAMP7 | chrX | 155876345 | 155948769 |
| NA19011 | hp2 | a0001 | c0001 | t0001 | g0107 | EAS | JPT | VAMP7_chrX_155876345_155948769 | VAMP7 | chrX | 155876345 | 155948769 |
| NA19030 | hp1 | a0001 | c0001 | t0001 | g0076 | AFR | LWK | VAMP7_chrX_155876345_155948769 | VAMP7 | chrX | 155876345 | 155948769 |
| NA19030 | hp2 | a0001 | c0001 | t0001 | g0142 | AFR | LWK | VAMP7_chrX_155876345_155948769 | VAMP7 | chrX | 155876345 | 155948769 |
| NA19055 | hp1 | a0001 | c0001 | t0001 | g0095 | EAS | JPT | VAMP7_chrX_155876345_155948769 | VAMP7 | chrX | 155876345 | 155948769 |
| NA19057 | hp1 | a0001 | c0001 | t0001 | g0051 | EAS | JPT | VAMP7_chrX_155876345_155948769 | VAMP7 | chrX | 155876345 | 155948769 |
| NA19057 | hp2 | a0001 | c0001 | t0001 | g0102 | EAS | JPT | VAMP7_chrX_155876345_155948769 | VAMP7 | chrX | 155876345 | 155948769 |
| NA19060 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | VAMP7_chrX_155876345_155948769 | VAMP7 | chrX | 155876345 | 155948769 |
| NA19062 | hp1 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | VAMP7_chrX_155876345_155948769 | VAMP7 | chrX | 155876345 | 155948769 |
| NA19067 | hp1 | a0001 | c0001 | t0001 | g0091 | 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 | g0002 | 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 | g0012 | EAS | JPT | VAMP7_chrX_155876345_155948769 | VAMP7 | chrX | 155876345 | 155948769 |
| NA19080 | hp1 | a0001 | c0001 | t0001 | g0100 | EAS | JPT | VAMP7_chrX_155876345_155948769 | VAMP7 | chrX | 155876345 | 155948769 |
| NA19080 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | VAMP7_chrX_155876345_155948769 | VAMP7 | chrX | 155876345 | 155948769 |
| NA19085 | hp2 | a0001 | c0001 | t0001 | g0025 | EAS | JPT | VAMP7_chrX_155876345_155948769 | VAMP7 | chrX | 155876345 | 155948769 |
| NA19088 | hp1 | a0001 | c0001 | t0007 | g0092 | EAS | JPT | VAMP7_chrX_155876345_155948769 | VAMP7 | chrX | 155876345 | 155948769 |
| NA19089 | hp1 | a0001 | c0001 | t0001 | g0045 | EAS | JPT | VAMP7_chrX_155876345_155948769 | VAMP7 | chrX | 155876345 | 155948769 |
| NA19090 | hp1 | a0001 | c0001 | t0001 | g0145 | EAS | JPT | VAMP7_chrX_155876345_155948769 | VAMP7 | chrX | 155876345 | 155948769 |
| NA19090 | hp2 | a0001 | c0001 | t0001 | g0089 | EAS | JPT | VAMP7_chrX_155876345_155948769 | VAMP7 | chrX | 155876345 | 155948769 |
| NA19240 | hp1 | a0001 | c0001 | t0001 | g0005 | AFR | YRI | VAMP7_chrX_155876345_155948769 | VAMP7 | chrX | 155876345 | 155948769 |
| NA19240 | hp2 | a0001 | c0001 | t0001 | g0073 | AFR | YRI | VAMP7_chrX_155876345_155948769 | VAMP7 | chrX | 155876345 | 155948769 |
| NA20129 | hp1 | a0001 | c0001 | t0001 | g0079 | AFR | ASW | VAMP7_chrX_155876345_155948769 | VAMP7 | chrX | 155876345 | 155948769 |
| NA20129 | hp2 | a0001 | c0001 | t0001 | g0098 | AFR | ASW | VAMP7_chrX_155876345_155948769 | VAMP7 | chrX | 155876345 | 155948769 |
| HG01123 | hp1 | a0001 | c0001 | t0001 | g0101 | AMR | CLM | VAMP7_chrX_155876345_155948769 | VAMP7 | chrX | 155876345 | 155948769 |
| HG01123 | hp2 | a0001 | c0001 | t0001 | g0085 | AMR | CLM | VAMP7_chrX_155876345_155948769 | VAMP7 | chrX | 155876345 | 155948769 |
| HG02109 | hp1 | a0001 | c0001 | t0001 | g0005 | AFR | ACB | VAMP7_chrX_155876345_155948769 | VAMP7 | chrX | 155876345 | 155948769 |
| HG02109 | hp2 | a0001 | c0001 | t0001 | g0013 | AFR | ACB | VAMP7_chrX_155876345_155948769 | VAMP7 | chrX | 155876345 | 155948769 |
| HG02559 | hp1 | a0001 | c0001 | t0001 | g0055 | 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 | g0013 | AFR | MSL | VAMP7_chrX_155876345_155948769 | VAMP7 | chrX | 155876345 | 155948769 |
| HG06807 | hp1 | a0001 | c0001 | t0001 | g0061 | AFR | USA | VAMP7_chrX_155876345_155948769 | VAMP7 | chrX | 155876345 | 155948769 |
| HG06807 | hp2 | a0001 | c0001 | t0001 | g0070 | AFR | USA | VAMP7_chrX_155876345_155948769 | VAMP7 | chrX | 155876345 | 155948769 |
| NA18955 | hp1 | a0001 | c0001 | t0001 | g0108 | EAS | JPT | VAMP7_chrX_155876345_155948769 | VAMP7 | chrX | 155876345 | 155948769 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0001 | g0020 | REF | REF | VAMP7_chrX_155876345_155948769 | VAMP7 | chrX | 155876345 | 155948769 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0001 | g0116 | REF | REF | VAMP7_chrX_155876345_155948769 | VAMP7 | chrX | 155876345 | 155948769 |
| view | 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 |
|---|
| view | 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 |
| view | 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 |
| view | 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:155881674 | A | G | 1 | a0001c0001t0001g0154 | 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 | a0001c0001t0001g0150 a0001c0001t0001g0151 a0001c0001t0001g0152 others(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 | a0001c0001t0001g0005 a0001c0001t0001g0149 |
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 | a0001c0001t0001g0022 a0001c0001t0001g0024 a0001c0001t0001g0025 others(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 | a0001c0001t0001g0154 | 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 | a0001c0001t0001g0032 a0001c0001t0001g0033 a0001c0001t0001g0034 others(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 | a0001c0001t0001g0143 a0001c0001t0001g0144 a0001c0001t0001g0145 others(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 | a0001c0001t0006g0021 | 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 | a0001c0001t0001g0154 | 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 | a0001c0001t0001g0141 a0001c0001t0001g0142 |
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 | a0001c0002t0001g0029 a0001c0002t0001g0030 a0001c0002t0001g0031 |
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:155882647 | A | G | 1 | a0001c0001t0001g0140 | 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 | a0001c0001t0001g0022 | 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 | 1 | a0001c0001t0002g0001 | 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 | a0001c0001t0001g0139 | 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 | a0001c0001t0001g0007 a0001c0001t0001g0039 a0001c0001t0001g0040 |
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 | a0001c0001t0001g0022 a0001c0001t0001g0024 a0001c0001t0001g0025 others(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 | a0001c0001t0001g0036 a0001c0001t0001g0037 a0001c0001t0001g0038 |
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 | CT | C | 12 | a0001c0001t0001g0026 a0001c0001t0001g0039 a0001c0001t0001g0041 others(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:155883857 | C | T | 1 | a0001c0001t0001g0138 | 1 | NA19001.hp1 | intron_variant | MODIFIER | c.-10+2409C>T | VAMP7 | ENSG00000124333.16 | transcript | ENST00000286448.12 | protein_coding | 1/7 | chrX | 155883857 | |||||||
| chrX:155884169 | C | G | 1 | a0001c0001t0001g0137 | 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 | a0001c0001t0001g0008 a0001c0001t0001g0041 a0001c0001t0001g0047 others(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 | a0001c0001t0001g0154 | 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 | a0001c0001t0001g0042 a0001c0001t0001g0049 |
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 | a0001c0001t0006g0021 | 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 | a0001c0001t0001g0032 a0001c0001t0001g0033 a0001c0001t0001g0034 others(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 | a0001c0001t0001g0022 | 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 | a0001c0001t0001g0050 | 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 | a0001c0001t0001g0148 | 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 | a0001c0001t0001g0154 | 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 | 10 | a0001c0001t0002g0001 a0001c0001t0002g0004 a0001c0001t0002g0019 others(7): 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 | a0001c0002t0001g0029 a0001c0002t0001g0030 a0001c0002t0001g0031 |
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 | a0001c0001t0001g0153 | 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 | a0001c0001t0001g0051 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.-9-3057G>C | VAMP7 | ENSG00000124333.16 | transcript | ENST00000286448.12 | protein_coding | 1/7 | chrX | 155886401 | |||||||
| chrX:155886936 | GGCT | G | 17 | a0001c0001t0001g0022 a0001c0001t0001g0024 a0001c0001t0001g0025 others(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 | a0001c0001t0001g0127 a0001c0001t0001g0128 a0001c0001t0001g0129 |
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 | a0001c0001t0002g0136 | 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 | a0001c0001t0001g0022 | 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 | a0001c0001t0001g0022 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.-9-2347C>T | VAMP7 | ENSG00000124333.16 | transcript | ENST00000286448.12 | protein_coding | 1/7 | chrX | 155887111 | |||||||
| chrX:155887348 | C | T | 3 | a0001c0002t0001g0029 a0001c0002t0001g0030 a0001c0002t0001g0031 |
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 | a0001c0001t0001g0153 | 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 | a0001c0001t0001g0032 a0001c0001t0001g0033 a0001c0001t0001g0034 others(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 | a0001c0001t0006g0021 | 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 | a0001c0001t0001g0022 a0001c0001t0001g0024 a0001c0001t0001g0025 others(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 | a0001c0001t0001g0126 | 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 | a0001c0001t0001g0016 a0001c0001t0001g0017 a0001c0001t0001g0018 others(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 | a0001c0001t0001g0024 a0001c0001t0001g0025 a0001c0001t0001g0026 others(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 | a0001c0001t0001g0026 a0001c0001t0001g0154 |
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 | a0001c0001t0001g0141 a0001c0001t0001g0142 |
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 | 16 | a0001c0001t0001g0027 a0001c0001t0001g0028 a0001c0001t0001g0041 others(13): Show |
16 | HG00639.hp2 HG00741.hp1 HG01071.hp1 others(13): Show |
intron_variant | MODIFIER | c.-9-1505dupA | VAMP7 | ENSG00000124333.16 | transcript | ENST00000286448.12 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chrX | 155887937 | ||||||
| chrX:155888030 | TG | T | 6 | a0001c0001t0001g0024 a0001c0001t0001g0025 a0001c0001t0006g0021 others(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 | a0001c0001t0006g0021 | 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 | a0001c0001t0001g0022 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.-9-1184C>T | VAMP7 | ENSG00000124333.16 | transcript | ENST00000286448.12 | protein_coding | 1/7 | chrX | 155888274 | |||||||
| chrX:155888299 | G | T | 1 | a0001c0001t0001g0154 | 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 | a0001c0001t0001g0154 | 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 | a0001c0001t0001g0123 | 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 | a0001c0001t0001g0022 | 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 | a0001c0001t0001g0122 | 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 | a0001c0001t0001g0024 a0001c0001t0001g0025 |
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 | a0001c0001t0001g0026 | 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 | a0001c0001t0001g0027 a0001c0001t0001g0028 |
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 | a0001c0001t0001g0008 a0001c0001t0001g0041 a0001c0001t0001g0047 others(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 | a0001c0001t0001g0154 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.146+213T>G | VAMP7 | ENSG00000124333.16 | transcript | ENST00000286448.12 | protein_coding | 2/7 | chrX | 155889825 | |||||||
| chrX:155889918 | CT | C | 5 | a0001c0001t0001g0024 a0001c0001t0001g0025 a0001c0002t0001g0029 others(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 | a0001c0001t0001g0046 a0001c0001t0001g0059 a0001c0001t0001g0060 others(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 | 88 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(85): 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 | a0001c0001t0001g0154 a0001c0001t0006g0021 |
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 | a0001c0001t0001g0058 | 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 | 10 | a0001c0001t0001g0005 a0001c0001t0001g0014 a0001c0001t0001g0024 others(7): 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 | 16 | a0001c0001t0001g0003 a0001c0001t0001g0100 a0001c0001t0001g0101 others(13): 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 | a0001c0001t0001g0097 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.146+858C>T | VAMP7 | ENSG00000124333.16 | transcript | ENST00000286448.12 | protein_coding | 2/7 | chrX | 155890470 | |||||||
| chrX:155890602 | TC | T | 15 | a0001c0001t0001g0002 a0001c0001t0001g0045 a0001c0001t0001g0086 others(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 | a0001c0001t0001g0154 | 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 | a0001c0001t0004g0023 | 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 | a0001c0001t0004g0023 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.146+1357C>T | VAMP7 | ENSG00000124333.16 | transcript | ENST00000286448.12 | protein_coding | 2/7 | chrX | 155890969 | |||||||
| chrX:155891146 | A | C | 1 | a0001c0001t0001g0154 | 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 | a0001c0001t0001g0107 | 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 | 97 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(94): 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 | a0001c0001t0001g0008 a0001c0001t0001g0041 a0001c0001t0001g0047 others(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 | a0001c0001t0001g0095 a0001c0001t0001g0096 |
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 | a0001c0001t0001g0086 a0001c0001t0001g0087 a0001c0001t0001g0088 |
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 | 92 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(89): 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 | a0001c0001t0001g0026 | 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 | a0001c0001t0001g0005 a0001c0001t0001g0149 |
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 | a0001c0001t0001g0022 | 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 | a0001c0002t0001g0029 a0001c0002t0001g0030 a0001c0002t0001g0031 |
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 | a0001c0001t0001g0085 | 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 | 4 | a0001c0001t0002g0001 a0001c0001t0002g0019 a0001c0001t0002g0134 others(1): 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 | 3 | a0001c0001t0001g0014 a0001c0001t0001g0098 a0001c0001t0001g0099 |
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 | a0001c0001t0001g0154 | 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 | 94 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(91): 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 | a0001c0001t0001g0027 a0001c0001t0001g0036 a0001c0001t0001g0037 others(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(5): Show |
1 | a0001c0001t0001g0033 | 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:155892774 | C | T | 3 | a0001c0001t0001g0007 a0001c0001t0001g0039 a0001c0001t0001g0040 |
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 | a0001c0001t0001g0033 a0001c0001t0001g0035 a0001c0001t0001g0036 others(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 | a0001c0001t0006g0021 | 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 | a0001c0001t0001g0152 | 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 | a0001c0001t0001g0005 a0001c0001t0001g0061 a0001c0001t0001g0063 others(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:155893301 | A | G | 2 | a0001c0001t0001g0026 a0001c0001t0006g0021 |
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 | a0001c0001t0001g0026 | 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 | a0001c0001t0001g0026 a0001c0001t0006g0021 |
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 | 87 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(84): 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 | a0001c0001t0001g0143 | 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 | a0001c0001t0001g0022 | 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 | 86 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(83): 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 | a0001c0001t0006g0021 | 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 | a0001c0001t0001g0002 a0001c0001t0001g0045 a0001c0001t0001g0080 others(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:155894313 | T | TG | 3 | a0001c0001t0001g0027 a0001c0001t0001g0028 a0001c0001t0004g0023 |
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 | a0001c0001t0001g0034 | 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 | a0001c0001t0001g0007 a0001c0001t0001g0039 a0001c0001t0001g0040 |
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 | a0001c0001t0002g0133 | 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 | a0001c0001t0001g0079 | 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 | a0001c0001t0001g0024 a0001c0001t0001g0025 |
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 | a0001c0001t0001g0024 a0001c0001t0001g0025 |
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 | a0001c0001t0006g0021 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.204+324G>A | VAMP7 | ENSG00000124333.16 | transcript | ENST00000286448.12 | protein_coding | 3/7 | chrX | 155896004 | |||||||
| chrX:155896395 | A | G | 92 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(89): 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 | a0001c0001t0001g0005 a0001c0001t0001g0061 a0001c0001t0001g0149 |
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 | a0001c0001t0001g0064 a0001c0001t0001g0077 a0001c0001t0001g0078 others(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 | a0001c0001t0001g0013 a0001c0001t0001g0032 a0001c0001t0001g0044 others(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:155896940 | C | T | 1 | a0001c0001t0004g0023 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.205-1172C>T | VAMP7 | ENSG00000124333.16 | transcript | ENST00000286448.12 | protein_coding | 3/7 | chrX | 155896940 | |||||||
| chrX:155897373 | T | C | 1 | a0001c0001t0001g0154 | 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 | a0001c0001t0001g0141 | 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 | a0001c0001t0001g0024 a0001c0001t0001g0025 a0001c0001t0001g0026 others(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 | a0001c0001t0001g0154 | 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 | a0001c0002t0001g0029 a0001c0002t0001g0030 a0001c0002t0001g0031 |
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 | a0001c0001t0001g0088 | 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 | 93 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(90): 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:155898390 | TA | T | 4 | a0001c0001t0001g0022 a0001c0001t0001g0026 a0001c0001t0001g0154 others(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 | 92 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(89): 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 | a0001c0001t0006g0021 | 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 | a0001c0001t0006g0021 | 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 | 96 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(93): 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 | 96 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(93): 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 | a0001c0001t0001g0154 | 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 | 2 | a0001c0001t0001g0056 a0001c0001t0001g0057 |
2 | HG01071.hp1 HG01081.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 | a0001c0001t0006g0021 | 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 | a0001c0001t0001g0026 | 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 | 96 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(93): 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 | a0001c0001t0001g0022 a0001c0001t0006g0021 |
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 | a0001c0001t0001g0036 | 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 | a0001c0002t0001g0029 a0001c0002t0001g0030 a0001c0002t0001g0031 |
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 | a0001c0001t0001g0013 a0001c0001t0001g0032 a0001c0001t0001g0044 others(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 | a0001c0001t0001g0147 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.343-1057C>T | VAMP7 | ENSG00000124333.16 | transcript | ENST00000286448.12 | protein_coding | 4/7 | chrX | 155899440 | |||||||
| chrX:155899542 | G | GCA | 92 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(89): 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 | 3 | a0001c0001t0001g0014 a0001c0001t0001g0098 a0001c0001t0001g0099 |
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 | 98 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(95): 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 | 97 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(94): 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 | a0001c0001t0001g0089 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.343-447C>T | VAMP7 | ENSG00000124333.16 | transcript | ENST00000286448.12 | protein_coding | 4/7 | chrX | 155900050 | |||||||
| chrX:155901127 | C | G | 1 | a0001c0001t0001g0146 | 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 | a0001c0001t0001g0154 | 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 | 91 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(88): 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 | a0001c0001t0001g0005 a0001c0001t0001g0061 a0001c0001t0001g0063 others(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 | a0001c0001t0001g0005 a0001c0001t0001g0061 a0001c0001t0001g0063 others(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 | a0001c0001t0001g0013 | 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 | a0001c0001t0001g0110 a0001c0001t0001g0121 |
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 | a0001c0001t0001g0007 a0001c0001t0001g0039 a0001c0001t0001g0040 |
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 | 88 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(85): 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 | a0001c0001t0001g0151 | 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 | 90 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(87): 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 | a0001c0001t0003g0112 | 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 | a0001c0001t0001g0125 | 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 | a0001c0001t0001g0075 | 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 | 97 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(94): 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 | a0001c0001t0001g0072 | 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 | 88 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(85): 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 | 98 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(95): 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:155902616 | A | G | 1 | a0001c0001t0004g0023 | 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 | a0001c0001t0001g0022 | 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 | a0001c0001t0001g0027 a0001c0001t0001g0028 a0001c0001t0001g0154 others(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 | 90 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(87): 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 | a0001c0001t0001g0026 | 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 | a0001c0001t0001g0107 | 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 | a0001c0001t0001g0142 | 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 | a0001c0001t0001g0064 a0001c0001t0001g0071 a0001c0001t0001g0077 others(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 | a0001c0001t0001g0063 | 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 | a0001c0001t0001g0154 a0001c0002t0001g0029 a0001c0002t0001g0030 others(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 | a0001c0001t0001g0027 a0001c0001t0001g0028 |
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 | a0001c0001t0001g0075 | 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 | 92 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(89): 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 | a0001c0001t0001g0139 | 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 | a0001c0002t0001g0029 a0001c0002t0001g0030 a0001c0002t0001g0031 |
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 | a0001c0001t0001g0111 | 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 | a0001c0001t0006g0021 | 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 | a0001c0001t0001g0027 a0001c0001t0001g0028 a0001c0001t0001g0154 others(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 | a0001c0001t0001g0025 | 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 | a0001c0001t0001g0105 | 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 | a0001c0001t0001g0154 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.433+3537A>G | VAMP7 | ENSG00000124333.16 | transcript | ENST00000286448.12 | protein_coding | 5/7 | chrX | 155904124 | |||||||
| chrX:155904360 | T | G | 1 | a0001c0001t0001g0034 | 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 | 97 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(94): 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 | a0001c0001t0001g0129 | 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 | 97 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(94): 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 | a0001c0001t0001g0144 | 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 | a0001c0002t0001g0029 a0001c0002t0001g0030 a0001c0002t0001g0031 |
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 | a0001c0001t0001g0026 a0001c0001t0001g0154 a0001c0001t0004g0023 |
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 | 95 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(92): 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:155904975 | G | A | 1 | a0001c0001t0004g0023 | 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 | a0001c0001t0001g0041 a0001c0001t0001g0047 a0001c0001t0001g0048 |
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:155905840 | T | C | 5 | a0001c0001t0001g0026 a0001c0001t0001g0027 a0001c0001t0001g0028 others(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:155906254 | A | G | 1 | a0001c0001t0001g0026 | 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 | 93 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(90): 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 | 87 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(84): 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 | a0001c0001t0001g0121 | 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 | 89 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(86): 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 | a0001c0001t0001g0154 | 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 | a0001c0001t0001g0084 | 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 | 97 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(94): 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 | a0001c0001t0001g0070 | 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 | 97 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(94): 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 | 97 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(94): 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 | a0001c0001t0006g0021 | 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 | a0001c0001t0001g0012 | 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:155907480 | C | T | 29 | a0001c0001t0001g0006 a0001c0001t0001g0009 a0001c0001t0001g0010 others(26): 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 | a0001c0001t0001g0053 | 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 | 86 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(83): 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 | a0001c0001t0001g0022 a0001c0001t0006g0021 |
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 | a0001c0001t0001g0027 a0001c0001t0001g0028 |
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 | a0001c0001t0001g0042 | 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 | a0001c0001t0001g0086 a0001c0001t0001g0087 a0001c0001t0001g0088 |
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 | a0001c0001t0001g0041 a0001c0001t0001g0047 |
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 | a0001c0001t0001g0032 | 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 | a0001c0001t0001g0050 | 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 | 87 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(84): 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:155908219 | G | A | 1 | a0001c0001t0006g0021 | 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 | a0001c0001t0001g0111 | 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 | a0001c0001t0001g0144 a0001c0001t0001g0145 a0001c0001t0001g0147 others(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 | a0001c0001t0001g0111 | 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 | a0001c0001t0001g0013 a0001c0001t0001g0073 |
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 | a0001c0002t0001g0029 a0001c0002t0001g0030 a0001c0002t0001g0031 |
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 | a0001c0001t0001g0038 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.433+7963C>T | VAMP7 | ENSG00000124333.16 | transcript | ENST00000286448.12 | protein_coding | 5/7 | chrX | 155908550 | |||||||
| chrX:155908615 | C | CTTTG | 98 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(95): 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 | a0001c0001t0001g0054 a0001c0001t0001g0113 |
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 | a0001c0001t0001g0069 a0001c0001t0001g0072 |
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 | 90 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(87): 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 | a0001c0002t0001g0029 a0001c0002t0001g0030 a0001c0002t0001g0031 |
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 | a0001c0001t0001g0026 | 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 | a0001c0001t0001g0005 a0001c0001t0001g0061 a0001c0001t0001g0063 others(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 | a0001c0001t0001g0036 a0001c0001t0001g0037 a0001c0001t0001g0038 |
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 | a0001c0001t0001g0119 a0001c0001t0001g0120 |
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 | a0001c0001t0001g0099 | 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 | a0001c0001t0001g0065 a0001c0001t0001g0081 |
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 | a0001c0001t0004g0023 | 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 | a0001c0001t0001g0042 a0001c0001t0001g0049 |
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 | a0001c0001t0001g0061 | 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 | a0001c0001t0001g0005 a0001c0001t0001g0061 a0001c0001t0001g0149 |
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 | a0001c0001t0001g0026 a0001c0001t0001g0027 a0001c0001t0001g0028 others(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:155910586 | G | GT | 5 | a0001c0001t0001g0026 a0001c0001t0001g0080 a0001c0002t0001g0029 others(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 | a0001c0001t0001g0036 a0001c0001t0001g0037 a0001c0001t0001g0038 others(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 | a0001c0001t0001g0026 a0001c0001t0001g0027 a0001c0001t0001g0028 others(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 | a0001c0001t0001g0002 a0001c0001t0001g0045 a0001c0001t0001g0080 others(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 | a0001c0001t0001g0086 a0001c0001t0001g0087 a0001c0001t0001g0088 |
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 | a0001c0001t0001g0049 | 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 | a0001c0001t0006g0021 | 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 | a0001c0002t0001g0029 a0001c0002t0001g0030 a0001c0002t0001g0031 |
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 | a0001c0001t0004g0023 | 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 | 98 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(95): 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 | 90 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(87): 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 | a0001c0001t0001g0022 | 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 | 98 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(95): 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 | 98 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(95): 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 | 10 | a0001c0001t0002g0001 a0001c0001t0002g0004 a0001c0001t0002g0019 others(7): 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 | a0001c0001t0001g0033 a0001c0001t0001g0035 |
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 | 98 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(95): 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 | a0001c0001t0001g0024 a0001c0001t0001g0025 a0001c0001t0001g0062 others(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 | 98 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(95): 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 | a0001c0001t0001g0022 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.434-6529A>G | VAMP7 | ENSG00000124333.16 | transcript | ENST00000286448.12 | protein_coding | 5/7 | chrX | 155913284 | |||||||
| chrX:155913609 | A | G | 94 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(91): 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 | a0001c0001t0001g0154 | 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 | a0001c0001t0001g0154 | 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 | 98 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(95): 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:155914082 | C | T | 98 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(95): 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 | a0001c0001t0006g0021 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.434-5654G>T | VAMP7 | ENSG00000124333.16 | transcript | ENST00000286448.12 | protein_coding | 5/7 | chrX | 155914159 | |||||||
| chrX:155914323 | T | A | 1 | a0001c0001t0001g0049 | 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 | a0001c0001t0001g0129 | 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 | a0001c0001t0006g0021 | 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 | a0001c0001t0001g0032 | 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 | a0001c0001t0001g0045 | 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 | 98 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(95): 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 | a0001c0001t0001g0022 | 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 | a0001c0001t0006g0021 | 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 | a0001c0001t0001g0022 a0001c0001t0001g0026 a0001c0001t0001g0154 others(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 | 83 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0007 others(80): 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 | a0001c0001t0001g0016 a0001c0001t0001g0017 a0001c0001t0001g0018 others(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 | a0001c0001t0001g0026 a0001c0001t0001g0154 |
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 | a0001c0001t0001g0154 a0001c0001t0004g0023 |
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 | a0001c0001t0001g0026 | 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 | a0001c0001t0001g0026 | 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 | 5 | a0001c0001t0002g0004 a0001c0001t0002g0130 a0001c0001t0002g0131 others(2): 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 | 95 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(92): 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 | a0001c0001t0003g0112 | 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 | a0001c0001t0001g0042 a0001c0001t0001g0049 |
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 | a0001c0001t0001g0012 | 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 | a0001c0001t0001g0150 a0001c0001t0001g0152 |
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 | a0001c0001t0004g0023 | 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 | a0001c0001t0001g0060 a0001c0001t0006g0021 |
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 | a0001c0002t0001g0029 a0001c0002t0001g0030 a0001c0002t0001g0031 |
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 | a0001c0001t0001g0022 | 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 | a0001c0001t0001g0109 a0001c0001t0001g0110 a0001c0001t0001g0118 others(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 | a0001c0001t0001g0002 a0001c0001t0001g0026 a0001c0001t0001g0045 others(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 | a0001c0001t0001g0122 | 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 | a0001c0001t0001g0046 a0001c0001t0001g0059 a0001c0001t0001g0060 |
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 | a0001c0001t0001g0026 | 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 | 90 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(87): 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 | a0001c0001t0001g0034 a0001c0001t0001g0088 |
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:155918365 | C | A | 1 | a0001c0001t0001g0022 | 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 | a0001c0001t0001g0022 | 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 | a0001c0001t0001g0022 | 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 | a0001c0001t0001g0045 | 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 | a0001c0001t0001g0022 | 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 | a0001c0001t0001g0056 a0001c0001t0001g0057 |
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:155918599 | C | T | 2 | a0001c0001t0001g0104 a0001c0001t0001g0117 |
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 | a0001c0001t0001g0022 | 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 | a0001c0001t0001g0068 | 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 | a0001c0001t0002g0132 | 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 | a0001c0001t0001g0075 a0001c0001t0001g0079 |
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 | a0001c0001t0001g0119 a0001c0001t0001g0120 |
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 | a0001c0001t0002g0132 | 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 | a0001c0001t0002g0132 | 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 | a0001c0001t0001g0100 | 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 | a0001c0001t0001g0033 a0001c0001t0001g0035 |
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 | a0001c0001t0001g0047 | 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 | a0001c0001t0001g0024 a0001c0001t0001g0025 a0001c0001t0001g0062 others(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 | 97 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(94): 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 | a0001c0001t0001g0154 a0001c0001t0004g0023 a0001c0002t0001g0029 others(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:155919414 | T | G | 1 | a0001c0001t0001g0022 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.434-399T>G | VAMP7 | ENSG00000124333.16 | transcript | ENST00000286448.12 | protein_coding | 5/7 | chrX | 155919414 | |||||||
| chrX:155919450 | A | G | 3 | a0001c0001t0001g0005 a0001c0001t0001g0061 a0001c0001t0001g0149 |
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 | a0001c0002t0001g0029 | 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 | a0001c0001t0001g0142 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.434-115C>T | VAMP7 | ENSG00000124333.16 | transcript | ENST00000286448.12 | protein_coding | 5/7 | chrX | 155919698 | |||||||
| chrX:155920332 | C | T | 1 | a0001c0001t0001g0022 | 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 | 98 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(95): 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 | 83 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0007 others(80): 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 | 90 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(87): 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 | a0001c0001t0001g0013 a0001c0001t0001g0032 a0001c0001t0001g0044 others(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 | a0001c0001t0001g0011 | 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:155921153 | T | C | 1 | a0001c0001t0001g0113 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.501+1273T>C | VAMP7 | ENSG00000124333.16 | transcript | ENST00000286448.12 | protein_coding | 6/7 | chrX | 155921153 | |||||||
| chrX:155921209 | G | C | 1 | a0001c0001t0006g0021 | 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 | a0001c0001t0002g0132 | 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 | 93 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(90): 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:155921422 | C | T | 90 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(87): 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:155922109 | T | G | 1 | a0001c0001t0002g0132 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.501+2229T>G | VAMP7 | ENSG00000124333.16 | transcript | ENST00000286448.12 | protein_coding | 6/7 | chrX | 155922109 | |||||||
| chrX:155922614 | G | A | 1 | a0001c0001t0001g0154 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.501+2734G>A | VAMP7 | ENSG00000124333.16 | transcript | ENST00000286448.12 | protein_coding | 6/7 | chrX | 155922614 | |||||||
| chrX:155922776 | T | C | 1 | a0001c0001t0001g0086 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.501+2896T>C | VAMP7 | ENSG00000124333.16 | transcript | ENST00000286448.12 | protein_coding | 6/7 | chrX | 155922776 | |||||||
| chrX:155922975 | C | T | 97 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(94): 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 | a0001c0001t0006g0021 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.501+3120T>C | VAMP7 | ENSG00000124333.16 | transcript | ENST00000286448.12 | protein_coding | 6/7 | chrX | 155923000 | |||||||
| chrX:155923285 | G | A | 1 | a0001c0001t0001g0154 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.501+3405G>A | VAMP7 | ENSG00000124333.16 | transcript | ENST00000286448.12 | protein_coding | 6/7 | chrX | 155923285 | |||||||
| chrX:155923426 | C | CT | 5 | a0001c0001t0001g0022 a0001c0001t0006g0021 a0001c0002t0001g0029 others(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:155923440 | A | C | 1 | a0001c0001t0001g0022 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.501+3560A>C | VAMP7 | ENSG00000124333.16 | transcript | ENST00000286448.12 | protein_coding | 6/7 | chrX | 155923440 | |||||||
| chrX:155923531 | T | C | 3 | a0001c0002t0001g0029 a0001c0002t0001g0030 a0001c0002t0001g0031 |
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 | a0001c0001t0002g0132 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.501+3662A>G | VAMP7 | ENSG00000124333.16 | transcript | ENST00000286448.12 | protein_coding | 6/7 | chrX | 155923542 | |||||||
| chrX:155923620 | T | C | 1 | a0001c0001t0006g0021 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.501+3740T>C | VAMP7 | ENSG00000124333.16 | transcript | ENST00000286448.12 | protein_coding | 6/7 | chrX | 155923620 | |||||||
| chrX:155924032 | A | G | 1 | a0001c0001t0001g0063 | 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 | a0001c0001t0001g0026 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.501+4252G>A | VAMP7 | ENSG00000124333.16 | transcript | ENST00000286448.12 | protein_coding | 6/7 | chrX | 155924132 | |||||||
| chrX:155924158 | T | A | 91 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(88): 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:155924284 | A | T | 1 | a0001c0001t0002g0132 | 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 | a0001c0001t0001g0071 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.501+4641T>G | VAMP7 | ENSG00000124333.16 | transcript | ENST00000286448.12 | protein_coding | 6/7 | chrX | 155924521 | |||||||
| chrX:155924853 | A | G | 1 | a0001c0001t0001g0041 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.501+4973A>G | VAMP7 | ENSG00000124333.16 | transcript | ENST00000286448.12 | protein_coding | 6/7 | chrX | 155924853 | |||||||
| chrX:155925097 | T | A | 1 | a0001c0001t0002g0132 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.501+5217T>A | VAMP7 | ENSG00000124333.16 | transcript | ENST00000286448.12 | protein_coding | 6/7 | chrX | 155925097 | |||||||
| chrX:155925655 | C | T | 1 | a0001c0001t0002g0131 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.501+5775C>T | VAMP7 | ENSG00000124333.16 | transcript | ENST00000286448.12 | protein_coding | 6/7 | chrX | 155925655 | |||||||
| chrX:155925804 | A | C | 1 | a0001c0001t0002g0132 | 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 | a0001c0001t0002g0132 | 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 | a0001c0001t0002g0132 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.501+5927T>G | VAMP7 | ENSG00000124333.16 | transcript | ENST00000286448.12 | protein_coding | 6/7 | chrX | 155925807 | |||||||
| chrX:155925884 | A | G | 1 | a0001c0001t0001g0036 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.501+6004A>G | VAMP7 | ENSG00000124333.16 | transcript | ENST00000286448.12 | protein_coding | 6/7 | chrX | 155925884 | |||||||
| chrX:155925897 | A | AACG | 6 | a0001c0001t0001g0013 a0001c0001t0001g0032 a0001c0001t0001g0044 others(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 | a0001c0001t0001g0054 a0001c0001t0001g0113 |
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:155925964 | A | G | 1 | a0001c0001t0001g0026 | 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 | 92 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(89): 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 | 90 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(87): 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 | a0001c0001t0001g0073 | 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 | a0001c0002t0001g0029 a0001c0002t0001g0030 a0001c0002t0001g0031 |
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 | a0001c0001t0001g0095 | 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 | 96 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(93): 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 | 90 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(87): 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 | a0001c0001t0001g0022 | 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 | 76 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0008 others(73): 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 | a0001c0001t0001g0005 a0001c0001t0001g0022 a0001c0001t0001g0149 |
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 | a0001c0001t0001g0075 a0001c0001t0001g0154 |
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 | 2 | a0001c0001t0002g0001 a0001c0001t0002g0135 |
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 | a0001c0001t0001g0026 a0001c0001t0001g0034 a0001c0001t0001g0054 others(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 | CA | C | 5 | a0001c0001t0001g0033 a0001c0001t0001g0035 a0001c0001t0001g0036 others(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 | CAAAAAAA others(4): Show |
C | 8 | a0001c0001t0001g0022 a0001c0001t0001g0028 a0001c0001t0001g0071 others(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 | 85 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(82): 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 | a0001c0001t0001g0009 a0001c0001t0001g0069 a0001c0001t0001g0072 |
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:155927765 | G | GT | 42 | a0001c0001t0001g0006 a0001c0001t0001g0009 a0001c0001t0001g0010 others(39): 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 | 51 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0007 others(48): 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:155927772 | T | G | 1 | a0001c0001t0001g0022 | 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 | a0001c0001t0001g0022 | 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 | a0001c0001t0001g0119 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.501+7949T>C | VAMP7 | ENSG00000124333.16 | transcript | ENST00000286448.12 | protein_coding | 6/7 | chrX | 155927829 | |||||||
| chrX:155928279 | T | C | 1 | a0001c0001t0001g0152 | 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 | a0001c0001t0006g0021 | 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 | a0001c0001t0001g0103 | 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 | 90 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(87): 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:155928826 | A | G | 97 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(94): 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 | 98 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(95): 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 | a0001c0001t0001g0148 | 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 | a0001c0001t0001g0026 | 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 | a0001c0001t0001g0128 | 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 | a0001c0001t0001g0113 | 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 | a0001c0001t0001g0026 | 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 | a0001c0001t0001g0040 | 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 | a0001c0001t0001g0138 | 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 | a0001c0001t0001g0042 a0001c0001t0001g0086 |
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 | a0001c0001t0001g0114 a0001c0001t0001g0119 a0001c0001t0001g0120 |
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 | a0001c0001t0001g0005 a0001c0001t0001g0061 a0001c0001t0001g0063 others(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 | a0001c0001t0006g0021 | 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 | a0001c0001t0001g0127 | 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 | 97 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(94): 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 | a0001c0001t0001g0026 | 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 | a0001c0002t0001g0029 a0001c0002t0001g0030 a0001c0002t0001g0031 |
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 | a0001c0001t0001g0124 | 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 | 8 | a0001c0001t0001g0046 a0001c0001t0001g0053 a0001c0001t0001g0055 others(5): Show |
8 | HG00639.hp2 HG00741.hp1 HG01071.hp1 others(5): 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 | CA | C | 17 | a0001c0001t0001g0013 a0001c0001t0001g0018 a0001c0001t0001g0022 others(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 | 85 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(82): 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 | a0001c0001t0001g0123 | 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 | a0001c0001t0001g0013 a0001c0001t0001g0032 a0001c0001t0001g0044 others(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 | 83 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(80): 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 | a0001c0001t0004g0023 | 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 | a0001c0001t0001g0139 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.502-9157G>A | VAMP7 | ENSG00000124333.16 | transcript | ENST00000286448.12 | protein_coding | 6/7 | chrX | 155930544 | |||||||
| chrX:155930663 | A | AG | 4 | a0001c0001t0006g0021 a0001c0002t0001g0029 a0001c0002t0001g0030 others(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 | a0001c0001t0002g0134 | 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 | T | 101 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(98): 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:155930719 | T | A | 1 | a0001c0001t0001g0144 | 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 | a0001c0001t0001g0053 | 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 | a0001c0001t0001g0005 a0001c0001t0001g0061 a0001c0001t0001g0149 |
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 | a0001c0001t0001g0026 | 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 | a0001c0001t0001g0026 | 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 | a0001c0001t0001g0035 | 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 | a0001c0001t0001g0039 | 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 | a0001c0001t0001g0022 | 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 | a0001c0001t0001g0058 | 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 | a0001c0001t0001g0026 a0001c0001t0006g0021 |
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:155931680 | G | A | 1 | a0001c0001t0001g0148 | 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 | a0001c0002t0001g0029 a0001c0002t0001g0030 a0001c0002t0001g0031 |
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 | a0001c0001t0001g0022 | 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 | a0001c0001t0001g0139 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.502-7866T>C | VAMP7 | ENSG00000124333.16 | transcript | ENST00000286448.12 | protein_coding | 6/7 | chrX | 155931835 | |||||||
| chrX:155931963 | G | T | 92 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(89): 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 | a0001c0001t0001g0022 | 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 | a0001c0001t0001g0121 | 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 | a0001c0001t0001g0026 | 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 | a0001c0002t0001g0029 a0001c0002t0001g0030 a0001c0002t0001g0031 |
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 | a0001c0001t0002g0130 | 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 | a0001c0001t0001g0022 | 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 | 98 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(95): 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 | a0001c0001t0001g0118 a0001c0001t0001g0123 |
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 | a0001c0001t0001g0061 | 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 | 96 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(93): 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 | a0001c0001t0001g0026 | 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 | a0001c0001t0001g0154 | 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 | a0001c0001t0006g0021 | 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 | a0001c0001t0001g0056 | 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 | a0001c0001t0001g0142 | 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 | a0001c0001t0004g0023 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.502-6437T>C | VAMP7 | ENSG00000124333.16 | transcript | ENST00000286448.12 | protein_coding | 6/7 | chrX | 155933264 | |||||||
| chrX:155933384 | T | C | 2 | a0001c0001t0001g0154 a0001c0001t0004g0023 |
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 | a0001c0001t0001g0022 | 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 | a0001c0001t0001g0062 | 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 | a0001c0001t0006g0021 | 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 | a0001c0001t0001g0045 | 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 | a0001c0001t0006g0021 | 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 | a0001c0001t0001g0075 a0001c0001t0001g0079 |
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 | a0001c0001t0001g0075 a0001c0001t0001g0079 |
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 | a0001c0001t0001g0075 a0001c0001t0001g0079 |
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 | a0001c0001t0001g0075 a0001c0001t0001g0079 |
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 | a0001c0001t0004g0023 | 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 | 20 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0027 others(17): 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 | a0001c0001t0001g0022 a0001c0001t0006g0021 a0001c0002t0001g0029 others(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 | a0001c0001t0001g0022 | 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 | a0001c0001t0001g0106 | 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 | a0001c0001t0001g0058 | 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 | a0001c0001t0001g0095 a0001c0001t0001g0096 |
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 | a0001c0001t0001g0115 | 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 | 90 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(87): 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 | 96 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(93): 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 | 95 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(92): 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 | a0001c0001t0001g0036 | 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 | 3 | a0001c0001t0001g0014 a0001c0001t0001g0098 a0001c0001t0001g0099 |
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 | a0001c0001t0002g0134 | 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 | a0001c0001t0001g0051 a0001c0001t0001g0067 a0001c0001t0001g0088 |
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 | a0001c0001t0006g0021 | 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 | a0001c0001t0001g0055 | 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 | a0001c0001t0001g0109 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.502-3927G>A | VAMP7 | ENSG00000124333.16 | transcript | ENST00000286448.12 | protein_coding | 6/7 | chrX | 155935774 | |||||||
| chrX:155936249 | T | A | 1 | a0001c0001t0001g0022 | 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 | a0001c0001t0001g0093 | 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 | a0001c0001t0001g0051 a0001c0001t0001g0067 a0001c0001t0001g0078 others(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 | 98 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(95): 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 | a0001c0001t0001g0005 a0001c0001t0001g0061 a0001c0001t0001g0063 others(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 | a0001c0001t0001g0062 | 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 | a0001c0001t0001g0154 | 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 | a0001c0001t0001g0148 | 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 | 2 | a0001c0001t0001g0010 a0001c0001t0001g0043 |
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 | a0001c0002t0001g0029 a0001c0002t0001g0030 a0001c0002t0001g0031 |
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 | a0001c0002t0001g0029 a0001c0002t0001g0030 a0001c0002t0001g0031 |
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 | a0001c0001t0004g0023 | 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 | a0001c0001t0001g0113 | 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 | a0001c0001t0004g0023 | 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 | a0001c0001t0001g0033 a0001c0001t0001g0035 |
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 | 92 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(89): 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 | a0001c0001t0001g0063 | 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 | a0001c0001t0001g0022 a0001c0001t0001g0026 a0001c0001t0006g0021 others(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 | a0001c0001t0001g0075 a0001c0001t0001g0079 |
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:155938668 | G | A | 1 | a0001c0001t0001g0026 | 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 | a0001c0001t0001g0005 | 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 | a0001c0001t0001g0139 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.502-1029C>G | VAMP7 | ENSG00000124333.16 | transcript | ENST00000286448.12 | protein_coding | 6/7 | chrX | 155938672 | |||||||
| chrX:155939060 | T | C | 1 | a0001c0001t0006g0021 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.502-641T>C | VAMP7 | ENSG00000124333.16 | transcript | ENST00000286448.12 | protein_coding | 6/7 | chrX | 155939060 | |||||||
| chrX:155939162 | C | T | 1 | a0001c0001t0002g0130 | 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 | a0001c0001t0001g0026 | 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 | a0001c0001t0001g0022 | 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 | a0001c0001t0001g0022 | 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 | a0001c0001t0001g0142 | 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 | a0001c0001t0001g0054 | 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 | a0001c0001t0001g0022 a0001c0001t0006g0021 a0001c0002t0001g0029 others(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 | 83 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0007 others(80): 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 | a0001c0001t0001g0017 | 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 | a0001c0001t0001g0033 a0001c0001t0001g0035 a0001c0001t0001g0036 others(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 | a0001c0001t0006g0021 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.594+236G>C | VAMP7 | ENSG00000124333.16 | transcript | ENST00000286448.12 | protein_coding | 7/7 | chrX | 155940029 | |||||||
| chrX:155940677 | T | C | 1 | a0001c0001t0001g0040 | 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 | 90 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(87): 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 | a0001c0001t0001g0016 a0001c0001t0001g0017 a0001c0001t0001g0018 others(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 | a0001c0001t0004g0023 | 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 | a0001c0001t0001g0005 a0001c0001t0001g0026 a0001c0001t0001g0149 |
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:155941229 | A | T | 4 | a0001c0001t0001g0144 a0001c0001t0001g0145 a0001c0001t0001g0147 others(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 | a0001c0001t0007g0092 | 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 | 90 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(87): 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 | a0001c0001t0006g0021 | 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 | 56 | a0001c0001t0001g0003 a0001c0001t0001g0015 a0001c0001t0001g0016 others(53): Show |
63 | HG00099.hp1 HG00280.hp1 HG00408.hp2 others(60): Show |
intron_variant | MODIFIER | c.595-10G>C | VAMP7 | ENSG00000124333.16 | transcript | ENST00000286448.12 | protein_coding | 7/7 | chrX | 155941873 |