Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 81671 |
| ensemblid | ENSG00000062716.13 |
| hgncid | 29559 |
| symbol | VMP1 |
| name | vacuole membrane protein 1 |
| refseq_nuc | NM_030938.5 |
| refseq_prot | NP_112200.2 |
| ensembl_nuc | ENST00000262291.9 |
| ensembl_prot | ENSP00000262291.3 |
| mane_status | MANE Select |
| chr | chr17 |
| start | 59707654 |
| end | 59842255 |
| strand | + |
| ver | v1.2 |
| region | chr17:59707654-59842255 |
| region5000 | chr17:59702654-59847255 |
| regionname0 | VMP1_chr17_59707654_59842255 |
| regionname5000 | VMP1_chr17_59702654_59847255 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 406 | 285 | 86 | 49 | 112 | 6 | 30 | 84 | VMP1_chr17_59702654_59847255 | VMP1 | MAENG others(401): Show |
chr17 | 59702654 | 59847255 |
| a0002 | 0/0 | 406 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | VMP1_chr17_59702654_59847255 | VMP1 | MAENG others(401): Show |
chr17 | 59702654 | 59847255 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 1218 | 283 | 86 | 49 | 111 | 5 | 30 | VMP1_chr17_59702654_59847255 | VMP1 | ATGGC others(1213): Show |
chr17 | 59702654 | 59847255 | ||
| a0001c0002 | 0/0 | 1218 | 2 | 0 | 0 | 1 | 1 | 0 | VMP1_chr17_59702654_59847255 | VMP1 | ATGGC others(1213): Show |
chr17 | 59702654 | 59847255 | ||
| a0002c0003 | 0/0 | 1218 | 1 | 0 | 1 | 0 | 0 | 0 | VMP1_chr17_59702654_59847255 | VMP1 | ATGGC others(1213): Show |
chr17 | 59702654 | 59847255 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 1/0 | 3686 | 131 | 45 | 27 | 41 | 4 | 13 | VMP1_chr17_59702654_59847255 | VMP1 | GGGTT others(3681): Show |
chr17 | 59702654 | 59847255 |
| a0001c0001t0002 | 0/1 | 3686 | 70 | 3 | 11 | 46 | 1 | 8 | VMP1_chr17_59702654_59847255 | VMP1 | GGGTT others(3681): Show |
chr17 | 59702654 | 59847255 |
| a0001c0001t0003 | 0/0 | 3686 | 52 | 20 | 9 | 21 | 0 | 2 | VMP1_chr17_59702654_59847255 | VMP1 | GGGTT others(3681): Show |
chr17 | 59702654 | 59847255 |
| a0001c0001t0004 | 0/0 | 3686 | 11 | 10 | 1 | 0 | 0 | 0 | VMP1_chr17_59702654_59847255 | VMP1 | GGGTT others(3681): Show |
chr17 | 59702654 | 59847255 |
| a0001c0001t0005 | 0/0 | 3686 | 5 | 0 | 0 | 1 | 0 | 4 | VMP1_chr17_59702654_59847255 | VMP1 | GGGTT others(3681): Show |
chr17 | 59702654 | 59847255 |
| a0001c0001t0006 | 0/0 | 3686 | 4 | 4 | 0 | 0 | 0 | 0 | VMP1_chr17_59702654_59847255 | VMP1 | GGGTT others(3681): Show |
chr17 | 59702654 | 59847255 |
| a0001c0001t0007 | 0/0 | 3686 | 2 | 0 | 0 | 0 | 0 | 2 | VMP1_chr17_59702654_59847255 | VMP1 | GGGTT others(3681): Show |
chr17 | 59702654 | 59847255 |
| a0001c0001t0008 | 0/0 | 3686 | 2 | 2 | 0 | 0 | 0 | 0 | VMP1_chr17_59702654_59847255 | VMP1 | GGGTT others(3681): Show |
chr17 | 59702654 | 59847255 |
| a0001c0001t0009 | 0/0 | 3686 | 1 | 0 | 0 | 0 | 0 | 1 | VMP1_chr17_59702654_59847255 | VMP1 | GGGTT others(3681): Show |
chr17 | 59702654 | 59847255 |
| a0001c0001t0010 | 0/0 | 3686 | 1 | 0 | 1 | 0 | 0 | 0 | VMP1_chr17_59702654_59847255 | VMP1 | GGGTT others(3681): Show |
chr17 | 59702654 | 59847255 |
| a0001c0001t0011 | 0/0 | 3686 | 1 | 0 | 0 | 1 | 0 | 0 | VMP1_chr17_59702654_59847255 | VMP1 | GGGTT others(3681): Show |
chr17 | 59702654 | 59847255 |
| a0001c0001t0012 | 0/0 | 3686 | 1 | 0 | 0 | 1 | 0 | 0 | VMP1_chr17_59702654_59847255 | VMP1 | GGGTT others(3681): Show |
chr17 | 59702654 | 59847255 |
| a0001c0001t0013 | 0/0 | 3686 | 1 | 1 | 0 | 0 | 0 | 0 | VMP1_chr17_59702654_59847255 | VMP1 | GGGTT others(3681): Show |
chr17 | 59702654 | 59847255 |
| a0001c0001t0014 | 0/0 | 3686 | 1 | 1 | 0 | 0 | 0 | 0 | VMP1_chr17_59702654_59847255 | VMP1 | GGGTT others(3681): Show |
chr17 | 59702654 | 59847255 |
| a0001c0002t0001 | 0/0 | 3686 | 2 | 0 | 0 | 1 | 1 | 0 | VMP1_chr17_59702654_59847255 | VMP1 | GGGTT others(3681): Show |
chr17 | 59702654 | 59847255 |
| a0002c0003t0002 | 0/0 | 3686 | 1 | 0 | 1 | 0 | 0 | 0 | VMP1_chr17_59702654_59847255 | VMP1 | GGGTT others(3681): Show |
chr17 | 59702654 | 59847255 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0003 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| a0001c0001t0001g0004 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| a0001c0001t0001g0005 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| a0001c0001t0001g0006 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| a0001c0001t0001g0007 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| a0001c0001t0001g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| a0001c0001t0001g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| a0001c0001t0001g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| a0001c0001t0001g0011 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| a0001c0001t0001g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| a0001c0001t0001g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| a0001c0001t0001g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| a0001c0001t0001g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| a0001c0001t0001g0078 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| a0001c0001t0001g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| a0001c0001t0001g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| a0001c0001t0001g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| a0001c0001t0001g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| a0001c0001t0001g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| a0001c0001t0001g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| a0001c0001t0001g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| a0001c0001t0001g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| a0001c0001t0001g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| a0001c0001t0001g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| a0001c0001t0001g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| a0001c0001t0001g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| a0001c0001t0001g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| a0001c0001t0001g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| a0001c0001t0001g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| a0001c0001t0001g0100 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| a0001c0001t0001g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| a0001c0001t0001g0102 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| a0001c0001t0001g0103 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| a0001c0001t0001g0104 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| a0001c0001t0001g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| a0001c0001t0001g0132 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| a0001c0001t0001g0139 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| a0001c0001t0001g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| a0001c0001t0001g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| a0001c0001t0001g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| a0001c0001t0001g0158 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| a0001c0001t0001g0159 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| a0001c0001t0001g0160 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| a0001c0001t0001g0161 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| a0001c0001t0001g0162 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| a0001c0001t0001g0163 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| a0001c0001t0001g0164 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| a0001c0001t0001g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| a0001c0001t0001g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| a0001c0001t0001g0167 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| a0001c0001t0001g0168 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| a0001c0001t0001g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| a0001c0001t0001g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| a0001c0001t0001g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| a0001c0001t0001g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| a0001c0001t0001g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| a0001c0001t0001g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| a0001c0001t0001g0175 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| a0001c0001t0001g0176 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| a0001c0001t0001g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| a0001c0001t0001g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| a0001c0001t0001g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| a0001c0001t0001g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| a0001c0001t0001g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| a0001c0001t0001g0182 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| a0001c0001t0001g0183 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| a0001c0001t0001g0184 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| a0001c0001t0001g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| a0001c0001t0001g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| a0001c0001t0001g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| a0001c0001t0001g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| a0001c0001t0001g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| a0001c0001t0001g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| a0001c0001t0001g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| a0001c0001t0001g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| a0001c0001t0001g0199 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| a0001c0001t0001g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| a0001c0001t0001g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| a0001c0001t0001g0202 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| a0001c0001t0001g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| a0001c0001t0001g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| a0001c0001t0001g0205 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| a0001c0001t0001g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| a0001c0001t0001g0207 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| a0001c0001t0001g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| a0001c0001t0001g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| a0001c0001t0001g0210 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| a0001c0001t0001g0211 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| a0001c0001t0001g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| a0001c0001t0001g0213 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| a0001c0001t0001g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| a0001c0001t0001g0215 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| a0001c0001t0001g0217 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| a0001c0001t0001g0218 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| a0001c0001t0001g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| a0001c0001t0001g0220 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| a0001c0001t0001g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| a0001c0001t0001g0222 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| a0001c0001t0001g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| a0001c0001t0001g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| a0001c0001t0001g0225 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| a0001c0001t0001g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| a0001c0001t0001g0230 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| a0001c0001t0001g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| a0001c0001t0001g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| a0001c0001t0001g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| a0001c0001t0001g0237 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| a0001c0001t0001g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| a0001c0001t0001g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| a0001c0001t0001g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| a0001c0001t0001g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| a0001c0001t0001g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| a0001c0001t0001g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| a0001c0001t0001g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| a0001c0001t0001g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| a0001c0001t0001g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| a0001c0001t0001g0247 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| a0001c0001t0001g0248 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| a0001c0001t0001g0249 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| a0001c0001t0001g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| a0001c0001t0001g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| a0001c0001t0001g0252 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| a0001c0001t0001g0253 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| a0001c0001t0001g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| a0001c0001t0001g0255 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| a0001c0001t0001g0256 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| a0001c0001t0001g0276 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| a0001c0001t0001g0277 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| a0001c0001t0001g0278 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| a0001c0001t0001g0280 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| a0001c0001t0001g0282 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| a0001c0001t0002g0012 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| a0001c0001t0002g0013 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| a0001c0001t0002g0014 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| a0001c0001t0002g0015 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| a0001c0001t0002g0016 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| a0001c0001t0002g0017 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| a0001c0001t0002g0019 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| a0001c0001t0002g0020 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| a0001c0001t0002g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| a0001c0001t0002g0023 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| a0001c0001t0002g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| a0001c0001t0002g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| a0001c0001t0002g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| a0001c0001t0002g0027 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| a0001c0001t0002g0028 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| a0001c0001t0002g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| a0001c0001t0002g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| a0001c0001t0002g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| a0001c0001t0002g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| a0001c0001t0002g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| a0001c0001t0002g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| a0001c0001t0002g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| a0001c0001t0002g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| a0001c0001t0002g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| a0001c0001t0002g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| a0001c0001t0002g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| a0001c0001t0002g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| a0001c0001t0002g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| a0001c0001t0002g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| a0001c0001t0002g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| a0001c0001t0002g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| a0001c0001t0002g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| a0001c0001t0002g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| a0001c0001t0002g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| a0001c0001t0002g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| a0001c0001t0002g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| a0001c0001t0002g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| a0001c0001t0002g0052 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| a0001c0001t0002g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| a0001c0001t0002g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| a0001c0001t0002g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| a0001c0001t0002g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| a0001c0001t0002g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| a0001c0001t0002g0060 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| a0001c0001t0002g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| a0001c0001t0002g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| a0001c0001t0002g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| a0001c0001t0002g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| a0001c0001t0002g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| a0001c0001t0002g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| a0001c0001t0002g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| a0001c0001t0002g0071 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| a0001c0001t0002g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| a0001c0001t0002g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| a0001c0001t0002g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| a0001c0001t0002g0075 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| a0001c0001t0002g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| a0001c0001t0002g0094 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| a0001c0001t0002g0096 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| a0001c0001t0002g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| a0001c0001t0002g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| a0001c0001t0002g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| a0001c0001t0002g0192 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| a0001c0001t0002g0193 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| a0001c0001t0002g0194 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| a0001c0001t0002g0195 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| a0001c0001t0002g0196 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| a0001c0001t0002g0234 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| a0001c0001t0002g0235 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| a0001c0001t0002g0236 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| a0001c0001t0003g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| a0001c0001t0003g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| a0001c0001t0003g0108 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| a0001c0001t0003g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| a0001c0001t0003g0111 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| a0001c0001t0003g0112 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| a0001c0001t0003g0113 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| a0001c0001t0003g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| a0001c0001t0003g0115 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| a0001c0001t0003g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| a0001c0001t0003g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| a0001c0001t0003g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| a0001c0001t0003g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| a0001c0001t0003g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| a0001c0001t0003g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| a0001c0001t0003g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| a0001c0001t0003g0123 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| a0001c0001t0003g0124 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| a0001c0001t0003g0125 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| a0001c0001t0003g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| a0001c0001t0003g0127 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| a0001c0001t0003g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| a0001c0001t0003g0129 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| a0001c0001t0003g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| a0001c0001t0003g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| a0001c0001t0003g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| a0001c0001t0003g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| a0001c0001t0003g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| a0001c0001t0003g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| a0001c0001t0003g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| a0001c0001t0003g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| a0001c0001t0003g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| a0001c0001t0003g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| a0001c0001t0003g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| a0001c0001t0003g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| a0001c0001t0003g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| a0001c0001t0003g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| a0001c0001t0003g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| a0001c0001t0003g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| a0001c0001t0003g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| a0001c0001t0003g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| a0001c0001t0003g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| a0001c0001t0003g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| a0001c0001t0003g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| a0001c0001t0003g0156 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| a0001c0001t0003g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| a0001c0001t0003g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| a0001c0001t0003g0258 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| a0001c0001t0003g0259 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| a0001c0001t0003g0260 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| a0001c0001t0003g0261 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| a0001c0001t0003g0264 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| a0001c0001t0004g0262 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| a0001c0001t0004g0263 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| a0001c0001t0004g0265 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| a0001c0001t0004g0266 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| a0001c0001t0004g0267 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| a0001c0001t0004g0268 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| a0001c0001t0004g0269 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| a0001c0001t0004g0270 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| a0001c0001t0004g0271 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| a0001c0001t0004g0272 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| a0001c0001t0004g0273 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| a0001c0001t0005g0002 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| a0001c0001t0005g0018 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| a0001c0001t0005g0058 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| a0001c0001t0005g0059 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| a0001c0001t0005g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| a0001c0001t0006g0283 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| a0001c0001t0006g0284 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| a0001c0001t0006g0285 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| a0001c0001t0006g0286 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| a0001c0001t0007g0274 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| a0001c0001t0007g0275 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| a0001c0001t0008g0279 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| a0001c0001t0008g0281 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| a0001c0001t0009g0109 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| a0001c0001t0010g0228 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| a0001c0001t0011g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| a0001c0001t0012g0001 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| a0001c0001t0013g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| a0001c0001t0014g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| a0001c0002t0001g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| a0001c0002t0001g0227 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| a0002c0003t0002g0030 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00140 | hp1 | a0001 | c0001 | t0001 | g0168 | EUR | GBR | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| HG00140 | hp2 | a0001 | c0002 | t0001 | g0227 | EUR | GBR | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| HG00280 | hp1 | a0001 | c0001 | t0001 | g0222 | EUR | FIN | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| HG00280 | hp2 | a0001 | c0001 | t0001 | g0218 | EUR | FIN | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| HG00408 | hp1 | a0001 | c0001 | t0001 | g0106 | EAS | CHS | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| HG00408 | hp2 | a0001 | c0001 | t0002 | g0036 | EAS | CHS | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| HG00423 | hp1 | a0001 | c0001 | t0001 | g0179 | EAS | CHS | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| HG00423 | hp2 | a0001 | c0001 | t0002 | g0064 | EAS | CHS | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| HG00438 | hp1 | a0001 | c0001 | t0001 | g0177 | EAS | CHS | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| HG00438 | hp2 | a0001 | c0001 | t0003 | g0136 | EAS | CHS | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| HG00544 | hp1 | a0001 | c0001 | t0002 | g0049 | EAS | CHS | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| HG00544 | hp2 | a0001 | c0002 | t0001 | g0226 | EAS | CHS | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| HG00621 | hp1 | a0001 | c0001 | t0002 | g0041 | EAS | CHS | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| HG00621 | hp2 | a0001 | c0001 | t0001 | g0206 | EAS | CHS | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| HG00639 | hp1 | a0001 | c0001 | t0001 | g0211 | AMR | PUR | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| HG00639 | hp2 | a0002 | c0003 | t0002 | g0030 | AMR | PUR | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| HG00642 | hp1 | a0001 | c0001 | t0003 | g0113 | AMR | PUR | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| HG00642 | hp2 | a0001 | c0001 | t0001 | g0220 | AMR | PUR | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| HG00673 | hp1 | a0001 | c0001 | t0002 | g0048 | EAS | CHS | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| HG00673 | hp2 | a0001 | c0001 | t0003 | g0110 | EAS | CHS | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| HG00738 | hp1 | a0001 | c0001 | t0002 | g0019 | AMR | PUR | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| HG00738 | hp2 | a0001 | c0001 | t0003 | g0125 | AMR | PUR | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| HG00741 | hp1 | a0001 | c0001 | t0002 | g0235 | AMR | PUR | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| HG00741 | hp2 | a0001 | c0001 | t0010 | g0228 | AMR | PUR | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| HG01069 | hp1 | a0001 | c0001 | t0003 | g0127 | AMR | PUR | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| HG01069 | hp2 | a0001 | c0001 | t0002 | g0193 | AMR | PUR | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| HG01071 | hp1 | a0001 | c0001 | t0003 | g0111 | AMR | PUR | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| HG01071 | hp2 | a0001 | c0001 | t0002 | g0234 | AMR | PUR | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| HG01074 | hp1 | a0001 | c0001 | t0002 | g0192 | AMR | PUR | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| HG01074 | hp2 | a0001 | c0001 | t0001 | g0230 | AMR | PUR | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| HG01099 | hp1 | a0001 | c0001 | t0001 | g0007 | AMR | PUR | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| HG01099 | hp2 | a0001 | c0001 | t0001 | g0282 | AMR | PUR | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| HG01109 | hp1 | a0001 | c0001 | t0001 | g0237 | AMR | PUR | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| HG01109 | hp2 | a0001 | c0001 | t0004 | g0262 | AMR | PUR | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| HG01168 | hp1 | a0001 | c0001 | t0002 | g0020 | AMR | PUR | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| HG01168 | hp2 | a0001 | c0001 | t0003 | g0156 | AMR | PUR | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| HG01243 | hp1 | a0001 | c0001 | t0001 | g0078 | AMR | PUR | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| HG01243 | hp2 | a0001 | c0001 | t0001 | g0205 | AMR | PUR | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| HG01255 | hp1 | a0001 | c0001 | t0001 | g0162 | AMR | CLM | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| HG01255 | hp2 | a0001 | c0001 | t0001 | g0207 | AMR | CLM | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| HG01256 | hp1 | a0001 | c0001 | t0001 | g0163 | AMR | CLM | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| HG01256 | hp2 | a0001 | c0001 | t0001 | g0248 | AMR | CLM | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| HG01258 | hp1 | a0001 | c0001 | t0002 | g0194 | AMR | CLM | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| HG01258 | hp2 | a0001 | c0001 | t0001 | g0161 | AMR | CLM | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| HG01261 | hp1 | a0001 | c0001 | t0003 | g0115 | AMR | CLM | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| HG01261 | hp2 | a0001 | c0001 | t0001 | g0102 | AMR | CLM | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| HG01358 | hp1 | a0001 | c0001 | t0002 | g0196 | AMR | CLM | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| HG01358 | hp2 | a0001 | c0001 | t0001 | g0101 | AMR | CLM | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| HG01361 | hp1 | a0001 | c0001 | t0001 | g0104 | AMR | CLM | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| HG01361 | hp2 | a0001 | c0001 | t0001 | g0249 | AMR | CLM | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| HG01884 | hp1 | a0001 | c0001 | t0001 | g0008 | AFR | ACB | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| HG01884 | hp2 | a0001 | c0001 | t0001 | g0203 | AFR | ACB | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| HG01891 | hp1 | a0001 | c0001 | t0001 | g0172 | AFR | ACB | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| HG01891 | hp2 | a0001 | c0001 | t0001 | g0083 | AFR | ACB | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| HG01934 | hp1 | a0001 | c0001 | t0001 | g0158 | AMR | PEL | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| HG01934 | hp2 | a0001 | c0001 | t0003 | g0124 | AMR | PEL | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| HG01952 | hp1 | a0001 | c0001 | t0001 | g0167 | AMR | PEL | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| HG01952 | hp2 | a0001 | c0001 | t0001 | g0011 | AMR | PEL | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| HG01975 | hp1 | a0001 | c0001 | t0002 | g0094 | AMR | PEL | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| HG01975 | hp2 | a0001 | c0001 | t0001 | g0160 | AMR | PEL | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| HG01978 | hp1 | a0001 | c0001 | t0003 | g0129 | AMR | PEL | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| HG01978 | hp2 | a0001 | c0001 | t0001 | g0225 | AMR | PEL | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| HG01981 | hp1 | a0001 | c0001 | t0001 | g0175 | AMR | PEL | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| HG01981 | hp2 | a0001 | c0001 | t0002 | g0075 | AMR | PEL | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| HG02004 | hp1 | a0001 | c0001 | t0001 | g0159 | AMR | PEL | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| HG02004 | hp2 | a0001 | c0001 | t0001 | g0210 | AMR | PEL | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| HG02015 | hp1 | a0001 | c0001 | t0003 | g0121 | EAS | KHV | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| HG02015 | hp2 | a0001 | c0001 | t0002 | g0039 | EAS | KHV | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| HG02027 | hp1 | a0001 | c0001 | t0002 | g0034 | EAS | KHV | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| HG02027 | hp2 | a0001 | c0001 | t0003 | g0257 | EAS | KHV | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| HG02040 | hp1 | a0001 | c0001 | t0001 | g0224 | EAS | KHV | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| HG02040 | hp2 | a0001 | c0001 | t0002 | g0038 | EAS | KHV | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| HG02071 | hp1 | a0001 | c0001 | t0001 | g0246 | EAS | KHV | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| HG02071 | hp2 | a0001 | c0001 | t0003 | g0133 | EAS | KHV | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| HG02083 | hp1 | a0001 | c0001 | t0001 | g0219 | EAS | KHV | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| HG02083 | hp2 | a0001 | c0001 | t0002 | g0055 | EAS | KHV | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| HG02129 | hp1 | a0001 | c0001 | t0002 | g0054 | EAS | KHV | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| HG02129 | hp2 | a0001 | c0001 | t0001 | g0209 | EAS | KHV | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| HG02135 | hp1 | a0001 | c0001 | t0002 | g0015 | EAS | KHV | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| HG02135 | hp2 | a0001 | c0001 | t0001 | g0242 | EAS | KHV | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| HG02145 | hp1 | a0001 | c0001 | t0001 | g0241 | AFR | ACB | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| HG02145 | hp2 | a0001 | c0001 | t0008 | g0281 | AFR | ACB | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| HG02155 | hp1 | a0001 | c0001 | t0001 | g0251 | EAS | CDX | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| HG02155 | hp2 | a0001 | c0001 | t0002 | g0037 | EAS | CDX | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| HG02257 | hp1 | a0001 | c0001 | t0001 | g0152 | AFR | ACB | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| HG02257 | hp2 | a0001 | c0001 | t0003 | g0148 | AFR | ACB | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| HG02258 | hp1 | a0001 | c0001 | t0001 | g0229 | AFR | ACB | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| HG02258 | hp2 | a0001 | c0001 | t0001 | g0278 | AFR | ACB | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| HG02273 | hp1 | a0001 | c0001 | t0003 | g0123 | AMR | PEL | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| HG02273 | hp2 | a0001 | c0001 | t0001 | g0199 | AMR | PEL | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| HG02280 | hp1 | a0001 | c0001 | t0001 | g0188 | AFR | ACB | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| HG02280 | hp2 | a0001 | c0001 | t0001 | g0086 | AFR | ACB | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| HG02451 | hp1 | a0001 | c0001 | t0001 | g0255 | AFR | ACB | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| HG02451 | hp2 | a0001 | c0001 | t0001 | g0079 | AFR | ACB | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| HG02602 | hp1 | a0001 | c0001 | t0001 | g0182 | SAS | PJL | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| HG02602 | hp2 | a0001 | c0001 | t0002 | g0052 | SAS | PJL | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| HG02615 | hp1 | a0001 | c0001 | t0004 | g0273 | AFR | GWD | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| HG02615 | hp2 | a0001 | c0001 | t0003 | g0155 | AFR | GWD | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| HG02622 | hp1 | a0001 | c0001 | t0001 | g0090 | AFR | GWD | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| HG02622 | hp2 | a0001 | c0001 | t0001 | g0092 | AFR | GWD | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| HG02630 | hp1 | a0001 | c0001 | t0001 | g0077 | AFR | GWD | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| HG02630 | hp2 | a0001 | c0001 | t0003 | g0114 | AFR | GWD | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| HG02647 | hp1 | a0001 | c0001 | t0003 | g0105 | AFR | GWD | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| HG02647 | hp2 | a0001 | c0001 | t0001 | g0081 | AFR | GWD | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| HG02683 | hp1 | a0001 | c0001 | t0001 | g0213 | SAS | PJL | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| HG02683 | hp2 | a0001 | c0001 | t0002 | g0096 | SAS | PJL | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| HG02698 | hp1 | a0001 | c0001 | t0001 | g0139 | SAS | PJL | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| HG02698 | hp2 | a0001 | c0001 | t0005 | g0059 | SAS | PJL | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| HG02717 | hp1 | a0001 | c0001 | t0003 | g0140 | AFR | GWD | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| HG02717 | hp2 | a0001 | c0001 | t0001 | g0076 | AFR | GWD | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| HG02723 | hp1 | a0001 | c0001 | t0001 | g0277 | AFR | GWD | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| HG02723 | hp2 | a0001 | c0001 | t0001 | g0256 | AFR | GWD | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| HG02735 | hp1 | a0001 | c0001 | t0002 | g0023 | SAS | PJL | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| HG02735 | hp2 | a0001 | c0001 | t0001 | g0217 | SAS | PJL | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| HG02738 | hp1 | a0001 | c0001 | t0005 | g0002 | SAS | PJL | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| HG02738 | hp2 | a0001 | c0001 | t0001 | g0103 | SAS | PJL | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| HG02818 | hp1 | a0001 | c0001 | t0001 | g0280 | AFR | GWD | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| HG02818 | hp2 | a0001 | c0001 | t0001 | g0091 | AFR | GWD | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| HG02886 | hp1 | a0001 | c0001 | t0001 | g0201 | AFR | GWD | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| HG02886 | hp2 | a0001 | c0001 | t0001 | g0006 | AFR | GWD | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| HG02895 | hp1 | a0001 | c0001 | t0003 | g0146 | AFR | GWD | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| HG02895 | hp2 | a0001 | c0001 | t0003 | g0145 | AFR | GWD | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| HG02896 | hp1 | a0001 | c0001 | t0004 | g0267 | AFR | GWD | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| HG02896 | hp2 | a0001 | c0001 | t0003 | g0259 | AFR | GWD | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| HG02922 | hp1 | a0001 | c0001 | t0001 | g0208 | AFR | ESN | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| HG02922 | hp2 | a0001 | c0001 | t0001 | g0238 | AFR | ESN | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| HG02965 | hp1 | a0001 | c0001 | t0014 | g0189 | AFR | ESN | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| HG02965 | hp2 | a0001 | c0001 | t0004 | g0268 | AFR | ESN | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| HG02970 | hp1 | a0001 | c0001 | t0004 | g0265 | AFR | ESN | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| HG02970 | hp2 | a0001 | c0001 | t0003 | g0264 | AFR | ESN | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| HG03041 | hp1 | a0001 | c0001 | t0001 | g0170 | AFR | GWD | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| HG03041 | hp2 | a0001 | c0001 | t0004 | g0270 | AFR | GWD | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| HG03098 | hp1 | a0001 | c0001 | t0001 | g0276 | AFR | MSL | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| HG03098 | hp2 | a0001 | c0001 | t0001 | g0204 | AFR | MSL | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| HG03130 | hp1 | a0001 | c0001 | t0003 | g0137 | AFR | ESN | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| HG03130 | hp2 | a0001 | c0001 | t0006 | g0284 | AFR | ESN | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| HG03139 | hp1 | a0001 | c0001 | t0001 | g0169 | AFR | ESN | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| HG03139 | hp2 | a0001 | c0001 | t0001 | g0009 | AFR | ESN | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| HG03195 | hp1 | a0001 | c0001 | t0003 | g0151 | AFR | ESN | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| HG03195 | hp2 | a0001 | c0001 | t0001 | g0005 | AFR | ESN | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| HG03209 | hp1 | a0001 | c0001 | t0001 | g0080 | AFR | MSL | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| HG03209 | hp2 | a0001 | c0001 | t0003 | g0149 | AFR | MSL | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| HG03225 | hp1 | a0001 | c0001 | t0003 | g0154 | AFR | MSL | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| HG03225 | hp2 | a0001 | c0001 | t0001 | g0153 | AFR | MSL | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| HG03453 | hp1 | a0001 | c0001 | t0004 | g0266 | AFR | MSL | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| HG03453 | hp2 | a0001 | c0001 | t0001 | g0088 | AFR | MSL | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| HG03486 | hp1 | a0001 | c0001 | t0001 | g0004 | AFR | MSL | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| HG03486 | hp2 | a0001 | c0001 | t0004 | g0263 | AFR | MSL | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| HG03491 | hp1 | a0001 | c0001 | t0001 | g0215 | SAS | PJL | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| HG03491 | hp2 | a0001 | c0001 | t0007 | g0274 | SAS | PJL | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| HG03492 | hp1 | a0001 | c0001 | t0007 | g0275 | SAS | PJL | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| HG03492 | hp2 | a0001 | c0001 | t0001 | g0253 | SAS | PJL | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| HG03516 | hp1 | a0001 | c0001 | t0001 | g0010 | AFR | ESN | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| HG03516 | hp2 | a0001 | c0001 | t0004 | g0271 | AFR | ESN | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| HG03540 | hp1 | a0001 | c0001 | t0001 | g0003 | AFR | GWD | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| HG03540 | hp2 | a0001 | c0001 | t0001 | g0171 | AFR | GWD | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| HG03579 | hp1 | a0001 | c0001 | t0003 | g0134 | AFR | MSL | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| HG03579 | hp2 | a0001 | c0001 | t0002 | g0051 | AFR | MSL | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| HG03654 | hp1 | a0001 | c0001 | t0002 | g0012 | SAS | PJL | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| HG03654 | hp2 | a0001 | c0001 | t0001 | g0202 | SAS | PJL | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| HG03688 | hp1 | a0001 | c0001 | t0001 | g0247 | SAS | STU | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| HG03688 | hp2 | a0001 | c0001 | t0002 | g0013 | SAS | STU | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| HG03704 | hp1 | a0001 | c0001 | t0001 | g0183 | SAS | PJL | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| HG03704 | hp2 | a0001 | c0001 | t0002 | g0236 | SAS | PJL | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| HG03831 | hp1 | a0001 | c0001 | t0001 | g0184 | SAS | BEB | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| HG03831 | hp2 | a0001 | c0001 | t0009 | g0109 | SAS | BEB | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| HG03834 | hp1 | a0001 | c0001 | t0003 | g0112 | SAS | BEB | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| HG03834 | hp2 | a0001 | c0001 | t0002 | g0027 | SAS | BEB | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| HG03927 | hp1 | a0001 | c0001 | t0005 | g0058 | SAS | BEB | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| HG03927 | hp2 | a0001 | c0001 | t0003 | g0108 | SAS | BEB | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| HG03942 | hp1 | a0001 | c0001 | t0001 | g0176 | SAS | BEB | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| HG03942 | hp2 | a0001 | c0001 | t0005 | g0018 | SAS | BEB | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| HG04199 | hp1 | a0001 | c0001 | t0002 | g0060 | SAS | STU | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| HG04199 | hp2 | a0001 | c0001 | t0001 | g0132 | SAS | STU | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| NA18522 | hp1 | a0001 | c0001 | t0002 | g0022 | AFR | YRI | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| NA18522 | hp2 | a0001 | c0001 | t0004 | g0269 | AFR | YRI | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| NA18906 | hp1 | a0001 | c0001 | t0008 | g0279 | AFR | YRI | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| NA18906 | hp2 | a0001 | c0001 | t0004 | g0272 | AFR | YRI | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| NA18942 | hp1 | a0001 | c0001 | t0005 | g0061 | EAS | JPT | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| NA18942 | hp2 | a0001 | c0001 | t0001 | g0233 | EAS | JPT | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| NA18943 | hp1 | a0001 | c0001 | t0003 | g0120 | EAS | JPT | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| NA18943 | hp2 | a0001 | c0001 | t0001 | g0232 | EAS | JPT | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| NA18949 | hp1 | a0001 | c0001 | t0002 | g0062 | EAS | JPT | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| NA18949 | hp2 | a0001 | c0001 | t0003 | g0116 | EAS | JPT | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| NA18950 | hp1 | a0001 | c0001 | t0002 | g0073 | EAS | JPT | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| NA18950 | hp2 | a0001 | c0001 | t0003 | g0143 | EAS | JPT | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| NA18952 | hp1 | a0001 | c0001 | t0001 | g0197 | EAS | JPT | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| NA18952 | hp2 | a0001 | c0001 | t0002 | g0066 | EAS | JPT | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| NA18956 | hp1 | a0001 | c0001 | t0002 | g0067 | EAS | JPT | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| NA18956 | hp2 | a0001 | c0001 | t0001 | g0198 | EAS | JPT | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| NA18959 | hp1 | a0001 | c0001 | t0001 | g0254 | EAS | JPT | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| NA18959 | hp2 | a0001 | c0001 | t0003 | g0141 | EAS | JPT | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| NA18961 | hp1 | a0001 | c0001 | t0002 | g0047 | EAS | JPT | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| NA18961 | hp2 | a0001 | c0001 | t0012 | g0001 | EAS | JPT | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| NA18962 | hp1 | a0001 | c0001 | t0003 | g0138 | EAS | JPT | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| NA18962 | hp2 | a0001 | c0001 | t0002 | g0093 | EAS | JPT | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| NA18963 | hp1 | a0001 | c0001 | t0002 | g0031 | EAS | JPT | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| NA18963 | hp2 | a0001 | c0001 | t0001 | g0187 | EAS | JPT | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| NA18964 | hp1 | a0001 | c0001 | t0001 | g0223 | EAS | JPT | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| NA18964 | hp2 | a0001 | c0001 | t0002 | g0044 | EAS | JPT | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| NA18966 | hp1 | a0001 | c0001 | t0003 | g0128 | EAS | JPT | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| NA18966 | hp2 | a0001 | c0001 | t0001 | g0244 | EAS | JPT | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| NA18967 | hp1 | a0001 | c0001 | t0002 | g0017 | EAS | JPT | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| NA18967 | hp2 | a0001 | c0001 | t0003 | g0135 | EAS | JPT | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| NA18968 | hp1 | a0001 | c0001 | t0002 | g0040 | EAS | JPT | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| NA18968 | hp2 | a0001 | c0001 | t0001 | g0070 | EAS | JPT | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| NA18973 | hp1 | a0001 | c0001 | t0001 | g0181 | EAS | JPT | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| NA18973 | hp2 | a0001 | c0001 | t0002 | g0099 | EAS | JPT | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| NA18975 | hp1 | a0001 | c0001 | t0001 | g0240 | EAS | JPT | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| NA18975 | hp2 | a0001 | c0001 | t0002 | g0043 | EAS | JPT | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| NA18977 | hp1 | a0001 | c0001 | t0001 | g0212 | EAS | JPT | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| NA18977 | hp2 | a0001 | c0001 | t0002 | g0029 | EAS | JPT | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| NA18978 | hp1 | a0001 | c0001 | t0001 | g0150 | EAS | JPT | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| NA18978 | hp2 | a0001 | c0001 | t0002 | g0014 | EAS | JPT | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| NA18979 | hp1 | a0001 | c0001 | t0002 | g0033 | EAS | JPT | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| NA18979 | hp2 | a0001 | c0001 | t0001 | g0186 | EAS | JPT | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| NA18982 | hp1 | a0001 | c0001 | t0002 | g0097 | EAS | JPT | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| NA18982 | hp2 | a0001 | c0001 | t0001 | g0231 | EAS | JPT | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| NA18983 | hp1 | a0001 | c0001 | t0001 | g0185 | EAS | JPT | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| NA18983 | hp2 | a0001 | c0001 | t0002 | g0056 | EAS | JPT | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| NA18987 | hp1 | a0001 | c0001 | t0003 | g0142 | EAS | JPT | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| NA18987 | hp2 | a0001 | c0001 | t0002 | g0050 | EAS | JPT | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| NA18989 | hp1 | a0001 | c0001 | t0001 | g0174 | EAS | JPT | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| NA18989 | hp2 | a0001 | c0001 | t0002 | g0063 | EAS | JPT | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| NA18991 | hp1 | a0001 | c0001 | t0002 | g0016 | EAS | JPT | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| NA18991 | hp2 | a0001 | c0001 | t0003 | g0117 | EAS | JPT | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| NA18992 | hp1 | a0001 | c0001 | t0002 | g0098 | EAS | JPT | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| NA18992 | hp2 | a0001 | c0001 | t0003 | g0147 | EAS | JPT | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| NA18993 | hp1 | a0001 | c0001 | t0001 | g0173 | EAS | JPT | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| NA18993 | hp2 | a0001 | c0001 | t0002 | g0035 | EAS | JPT | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| NA19000 | hp1 | a0001 | c0001 | t0002 | g0065 | EAS | JPT | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| NA19000 | hp2 | a0001 | c0001 | t0001 | g0239 | EAS | JPT | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| NA19001 | hp1 | a0001 | c0001 | t0001 | g0191 | EAS | JPT | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| NA19001 | hp2 | a0001 | c0001 | t0003 | g0119 | EAS | JPT | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| NA19005 | hp1 | a0001 | c0001 | t0002 | g0072 | EAS | JPT | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| NA19005 | hp2 | a0001 | c0001 | t0001 | g0190 | EAS | JPT | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| NA19007 | hp1 | a0001 | c0001 | t0002 | g0046 | EAS | JPT | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| NA19007 | hp2 | a0001 | c0001 | t0001 | g0221 | EAS | JPT | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| NA19030 | hp1 | a0001 | c0001 | t0003 | g0258 | AFR | LWK | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| NA19030 | hp2 | a0001 | c0001 | t0006 | g0285 | AFR | LWK | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| NA19043 | hp1 | a0001 | c0001 | t0003 | g0144 | AFR | LWK | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| NA19043 | hp2 | a0001 | c0001 | t0001 | g0087 | AFR | LWK | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| NA19056 | hp1 | a0001 | c0001 | t0003 | g0126 | EAS | JPT | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| NA19056 | hp2 | a0001 | c0001 | t0001 | g0069 | EAS | JPT | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| NA19057 | hp1 | a0001 | c0001 | t0001 | g0214 | EAS | JPT | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| NA19057 | hp2 | a0001 | c0001 | t0002 | g0024 | EAS | JPT | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| NA19060 | hp1 | a0001 | c0001 | t0002 | g0025 | EAS | JPT | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| NA19060 | hp2 | a0001 | c0001 | t0001 | g0200 | EAS | JPT | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| NA19062 | hp1 | a0001 | c0001 | t0002 | g0045 | EAS | JPT | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| NA19062 | hp2 | a0001 | c0001 | t0003 | g0130 | EAS | JPT | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| NA19077 | hp1 | a0001 | c0001 | t0002 | g0057 | EAS | JPT | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| NA19077 | hp2 | a0001 | c0001 | t0001 | g0180 | EAS | JPT | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| NA19080 | hp1 | a0001 | c0001 | t0001 | g0178 | EAS | JPT | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| NA19080 | hp2 | a0001 | c0001 | t0003 | g0122 | EAS | JPT | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| NA19081 | hp1 | a0001 | c0001 | t0002 | g0042 | EAS | JPT | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| NA19081 | hp2 | a0001 | c0001 | t0001 | g0243 | EAS | JPT | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| NA19083 | hp1 | a0001 | c0001 | t0003 | g0107 | EAS | JPT | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| NA19083 | hp2 | a0001 | c0001 | t0002 | g0032 | EAS | JPT | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| NA19084 | hp1 | a0001 | c0001 | t0002 | g0026 | EAS | JPT | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| NA19084 | hp2 | a0001 | c0001 | t0001 | g0166 | EAS | JPT | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| NA19085 | hp1 | a0001 | c0001 | t0001 | g0245 | EAS | JPT | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| NA19085 | hp2 | a0001 | c0001 | t0011 | g0021 | EAS | JPT | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| NA19086 | hp1 | a0001 | c0001 | t0002 | g0053 | EAS | JPT | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| NA19086 | hp2 | a0001 | c0001 | t0003 | g0118 | EAS | JPT | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| NA19088 | hp1 | a0001 | c0001 | t0001 | g0250 | EAS | JPT | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| NA19088 | hp2 | a0001 | c0001 | t0002 | g0068 | EAS | JPT | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| NA20752 | hp1 | a0001 | c0001 | t0001 | g0100 | EUR | TSI | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| NA20752 | hp2 | a0001 | c0001 | t0002 | g0071 | EUR | TSI | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| HG01123 | hp1 | a0001 | c0001 | t0002 | g0028 | AMR | CLM | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| HG01123 | hp2 | a0001 | c0001 | t0001 | g0252 | AMR | CLM | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| HG02109 | hp1 | a0001 | c0001 | t0013 | g0216 | AFR | ACB | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| HG02109 | hp2 | a0001 | c0001 | t0006 | g0286 | AFR | ACB | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| HG02486 | hp1 | a0001 | c0001 | t0003 | g0157 | AFR | ACB | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| HG02486 | hp2 | a0001 | c0001 | t0001 | g0089 | AFR | ACB | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| HG02559 | hp1 | a0001 | c0001 | t0001 | g0082 | AFR | ACB | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| HG02559 | hp2 | a0001 | c0001 | t0001 | g0165 | AFR | ACB | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| HG03471 | hp1 | a0001 | c0001 | t0001 | g0095 | AFR | MSL | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| HG03471 | hp2 | a0001 | c0001 | t0003 | g0261 | AFR | MSL | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| HG06807 | hp1 | a0001 | c0001 | t0001 | g0084 | AFR | USA | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| HG06807 | hp2 | a0001 | c0001 | t0006 | g0283 | AFR | USA | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| NA20300 | hp1 | a0001 | c0001 | t0002 | g0074 | AFR | USA | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| NA20300 | hp2 | a0001 | c0001 | t0003 | g0131 | AFR | USA | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| NA21309 | hp1 | a0001 | c0001 | t0003 | g0260 | AFR | LWK | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| NA21309 | hp2 | a0001 | c0001 | t0001 | g0085 | AFR | LWK | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0002 | g0195 | REF | REF | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0001 | g0164 | REF | REF | VMP1_chr17_59702654_59847255 | VMP1 | chr17 | 59702654 | 59847255 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr17:59738847 | G | A | 1 | a0002 | 1 | HG00639.hp2 | missense_variant | MODERATE | c.314G>A | p.Arg105His | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 5/12 | 435/3686 | 314/1221 | 105/406 | chr17 | 59738847 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr17:59773765 | A | G | 1 | a0001c0002 | 2 | HG00140.hp2 HG00544.hp2 |
synonymous_variant | LOW | c.594A>G | p.Thr198Thr | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 7/12 | 715/3686 | 594/1221 | 198/406 | chr17 | 59773765 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr17:59839982 | G | A | 1 | a0001c0001t0009 | 1 | HG03831.hp2 | 3_prime_UTR_variant | MODIFIER | c.*71G>A | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 12/12 | 71 | chr17 | 59839982 | ||||||
| chr17:59840859 | G | A | 1 | a0001c0001t0010 | 1 | HG00741.hp2 | 3_prime_UTR_variant | MODIFIER | c.*948G>A | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 12/12 | 948 | chr17 | 59840859 | ||||||
| chr17:59840891 | C | T | 1 | a0001c0001t0014 | 1 | HG02965.hp1 | 3_prime_UTR_variant | MODIFIER | c.*980C>T | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 12/12 | 980 | chr17 | 59840891 | ||||||
| chr17:59841009 | T | C | 1 | a0001c0001t0004 | 11 | HG01109.hp2 HG02615.hp1 HG02896.hp1 others(8): Show |
3_prime_UTR_variant | MODIFIER | c.*1098T>C | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 12/12 | 1098 | chr17 | 59841009 | ||||||
| chr17:59841136 | G | A | 1 | a0001c0001t0011 | 1 | NA19085.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1225G>A | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 12/12 | 1225 | chr17 | 59841136 | ||||||
| chr17:59841221 | G | C | 2 | a0001c0001t0005 a0001c0001t0007 |
7 | HG02698.hp2 HG02738.hp1 HG03491.hp2 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*1310G>C | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 12/12 | 1310 | chr17 | 59841221 | ||||||
| chr17:59841547 | T | C | 5 | a0001c0001t0002 a0001c0001t0005 a0001c0001t0007 others(2): Show |
78 | HG00408.hp2 HG00423.hp2 HG00544.hp1 others(75): Show |
3_prime_UTR_variant | MODIFIER | c.*1636T>C | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 12/12 | 1636 | chr17 | 59841547 | ||||||
| chr17:59841648 | C | G | 1 | a0001c0001t0007 | 2 | HG03491.hp2 HG03492.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1737C>G | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 12/12 | 1737 | chr17 | 59841648 | ||||||
| chr17:59841670 | A | T | 5 | a0001c0001t0002 a0001c0001t0005 a0001c0001t0007 others(2): Show |
78 | HG00408.hp2 HG00423.hp2 HG00544.hp1 others(75): Show |
3_prime_UTR_variant | MODIFIER | c.*1759A>T | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 12/12 | 1759 | chr17 | 59841670 | ||||||
| chr17:59841705 | G | A | 1 | a0001c0001t0012 | 1 | NA18961.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1794G>A | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 12/12 | 1794 | chr17 | 59841705 | ||||||
| chr17:59841938 | C | T | 1 | a0001c0001t0013 | 1 | HG02109.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2027C>T | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 12/12 | 2027 | chr17 | 59841938 | ||||||
| chr17:59842094 | T | G | 2 | a0001c0001t0003 a0001c0001t0009 |
53 | HG00438.hp2 HG00642.hp1 HG00673.hp2 others(50): Show |
3_prime_UTR_variant | MODIFIER | c.*2183T>G | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 12/12 | 2183 | chr17 | 59842094 | ||||||
| chr17:59842105 | A | G | 1 | a0001c0001t0006 | 4 | HG02109.hp2 HG03130.hp2 HG06807.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*2194A>G | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 12/12 | 2194 | chr17 | 59842105 | ||||||
| chr17:59842174 | A | G | 1 | a0001c0001t0008 | 2 | HG02145.hp2 NA18906.hp1 |
3_prime_UTR_variant | MODIFIER | c.*2263A>G | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 12/12 | 2263 | chr17 | 59842174 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr17:59707926 | G | C | 1 | a0001c0001t0012g0001 | 1 | NA18961.hp2 | intron_variant | MODIFIER | c.-27+178G>C | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 1/11 | chr17 | 59707926 | |||||||
| chr17:59707966 | C | T | 4 | a0001c0001t0006g0283 a0001c0001t0006g0284 a0001c0001t0006g0285 others(1): Show |
4 | HG02109.hp2 HG03130.hp2 HG06807.hp2 others(1): Show |
intron_variant | MODIFIER | c.-27+218C>T | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 1/11 | chr17 | 59707966 | |||||||
| chr17:59708356 | A | G | 1 | a0001c0001t0001g0282 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.-27+608A>G | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 1/11 | chr17 | 59708356 | |||||||
| chr17:59708408 | C | G | 4 | a0001c0001t0001g0278 a0001c0001t0001g0280 a0001c0001t0008g0279 others(1): Show |
4 | HG02145.hp2 HG02258.hp2 HG02818.hp1 others(1): Show |
intron_variant | MODIFIER | c.-27+660C>G | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 1/11 | chr17 | 59708408 | |||||||
| chr17:59708500 | C | A | 4 | a0001c0001t0006g0283 a0001c0001t0006g0284 a0001c0001t0006g0285 others(1): Show |
4 | HG02109.hp2 HG03130.hp2 HG06807.hp2 others(1): Show |
intron_variant | MODIFIER | c.-27+752C>A | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 1/11 | chr17 | 59708500 | |||||||
| chr17:59708809 | A | G | 1 | a0001c0001t0001g0277 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.-27+1061A>G | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 1/11 | chr17 | 59708809 | |||||||
| chr17:59709061 | C | A | 1 | a0001c0001t0005g0002 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.-27+1313C>A | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 1/11 | chr17 | 59709061 | |||||||
| chr17:59709142 | C | T | 1 | a0001c0001t0001g0276 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.-27+1394C>T | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 1/11 | chr17 | 59709142 | |||||||
| chr17:59709387 | G | T | 2 | a0001c0001t0007g0274 a0001c0001t0007g0275 |
2 | HG03491.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.-27+1639G>T | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 1/11 | chr17 | 59709387 | |||||||
| chr17:59709633 | C | T | 12 | a0001c0001t0003g0264 a0001c0001t0004g0262 a0001c0001t0004g0263 others(9): Show |
12 | HG01109.hp2 HG02615.hp1 HG02896.hp1 others(9): Show |
intron_variant | MODIFIER | c.-27+1885C>T | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 1/11 | chr17 | 59709633 | |||||||
| chr17:59709682 | A | G | 4 | a0001c0001t0003g0258 a0001c0001t0003g0259 a0001c0001t0003g0260 others(1): Show |
4 | HG02896.hp2 HG03471.hp2 NA19030.hp1 others(1): Show |
intron_variant | MODIFIER | c.-27+1934A>G | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 1/11 | chr17 | 59709682 | |||||||
| chr17:59709907 | T | C | 1 | a0001c0001t0001g0277 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.-27+2159T>C | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 1/11 | chr17 | 59709907 | |||||||
| chr17:59709956 | G | C | 1 | a0001c0001t0001g0003 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.-27+2208G>C | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 1/11 | chr17 | 59709956 | |||||||
| chr17:59710006 | G | C | 8 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(5): Show |
8 | HG01099.hp1 HG01884.hp1 HG01952.hp2 others(5): Show |
intron_variant | MODIFIER | c.-27+2258G>C | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 1/11 | chr17 | 59710006 | |||||||
| chr17:59710070 | G | C | 93 | a0001c0001t0001g0003 a0001c0001t0001g0069 a0001c0001t0001g0070 others(90): Show |
93 | HG00408.hp2 HG00423.hp2 HG00544.hp1 others(90): Show |
intron_variant | MODIFIER | c.-27+2322G>C | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 1/11 | chr17 | 59710070 | |||||||
| chr17:59710094 | G | C | 4 | a0001c0001t0001g0100 a0001c0001t0001g0101 a0001c0001t0001g0102 others(1): Show |
4 | HG01261.hp2 HG01358.hp2 HG02738.hp2 others(1): Show |
intron_variant | MODIFIER | c.-27+2346G>C | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 1/11 | chr17 | 59710094 | |||||||
| chr17:59710128 | C | T | 2 | a0001c0001t0002g0098 a0001c0001t0002g0099 |
2 | NA18973.hp2 NA18992.hp1 |
intron_variant | MODIFIER | c.-27+2380C>T | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 1/11 | chr17 | 59710128 | |||||||
| chr17:59710129 | G | A | 1 | a0001c0001t0001g0104 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.-27+2381G>A | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 1/11 | chr17 | 59710129 | |||||||
| chr17:59710403 | C | A | 3 | a0001c0001t0003g0264 a0001c0001t0004g0262 a0001c0001t0004g0263 |
3 | HG01109.hp2 HG02970.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.-27+2655C>A | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 1/11 | chr17 | 59710403 | |||||||
| chr17:59710449 | C | T | 1 | a0001c0001t0003g0257 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.-27+2701C>T | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 1/11 | chr17 | 59710449 | |||||||
| chr17:59710672 | T | A | 1 | a0001c0001t0003g0105 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.-27+2924T>A | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 1/11 | chr17 | 59710672 | |||||||
| chr17:59710836 | C | T | 2 | a0001c0001t0002g0096 a0001c0001t0002g0097 |
2 | HG02683.hp2 NA18982.hp1 |
intron_variant | MODIFIER | c.-27+3088C>T | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 1/11 | chr17 | 59710836 | |||||||
| chr17:59711011 | T | G | 1 | a0001c0001t0001g0106 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.-27+3263T>G | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 1/11 | chr17 | 59711011 | |||||||
| chr17:59711072 | C | CA | 91 | a0001c0001t0001g0003 a0001c0001t0001g0069 a0001c0001t0001g0070 others(88): Show |
91 | HG00408.hp2 HG00423.hp2 HG00544.hp1 others(88): Show |
intron_variant | MODIFIER | c.-27+3334dupA | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr17 | 59711072 | ||||||
| chr17:59711135 | C | CA | 94 | a0001c0001t0001g0003 a0001c0001t0001g0069 a0001c0001t0001g0070 others(91): Show |
94 | HG00408.hp2 HG00423.hp2 HG00544.hp1 others(91): Show |
intron_variant | MODIFIER | c.-27+3398dupA | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr17 | 59711135 | ||||||
| chr17:59711201 | T | C | 1 | a0001c0001t0002g0012 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.-27+3453T>C | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 1/11 | chr17 | 59711201 | |||||||
| chr17:59711247 | G | A | 22 | a0001c0001t0003g0110 a0001c0001t0003g0111 a0001c0001t0003g0112 others(19): Show |
22 | HG00642.hp1 HG00673.hp2 HG00738.hp2 others(19): Show |
intron_variant | MODIFIER | c.-27+3499G>A | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 1/11 | chr17 | 59711247 | |||||||
| chr17:59711419 | AACT | A | 94 | a0001c0001t0001g0100 a0001c0001t0001g0101 a0001c0001t0001g0102 others(91): Show |
94 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(91): Show |
intron_variant | MODIFIER | c.-27+3672_-27+3674d others(5): Show |
VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 1/11 | chr17 | 59711419 | |||||||
| chr17:59711423 | C | T | 94 | a0001c0001t0001g0100 a0001c0001t0001g0101 a0001c0001t0001g0102 others(91): Show |
94 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(91): Show |
intron_variant | MODIFIER | c.-27+3675C>T | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 1/11 | chr17 | 59711423 | |||||||
| chr17:59712845 | T | C | 250 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(247): Show |
250 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(247): Show |
intron_variant | MODIFIER | c.-27+5097T>C | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 1/11 | chr17 | 59712845 | |||||||
| chr17:59713266 | A | G | 93 | a0001c0001t0001g0003 a0001c0001t0001g0069 a0001c0001t0001g0070 others(90): Show |
93 | HG00408.hp2 HG00423.hp2 HG00544.hp1 others(90): Show |
intron_variant | MODIFIER | c.-27+5518A>G | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 1/11 | chr17 | 59713266 | |||||||
| chr17:59713479 | G | A | 1 | a0001c0001t0001g0282 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.-27+5731G>A | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 1/11 | chr17 | 59713479 | |||||||
| chr17:59713683 | CT | C | 64 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(61): Show |
64 | HG00438.hp2 HG00642.hp1 HG00673.hp2 others(61): Show |
intron_variant | MODIFIER | c.-27+5954delT | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr17 | 59713683 | ||||||
| chr17:59713683 | CTTT | C | 71 | a0001c0001t0001g0069 a0001c0001t0001g0070 a0001c0001t0002g0012 others(68): Show |
71 | HG00408.hp2 HG00423.hp2 HG00544.hp1 others(68): Show |
intron_variant | MODIFIER | c.-27+5952_-27+5954d others(5): Show |
VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr17 | 59713683 | ||||||
| chr17:59713683 | CTTTTTTT others(3): Show |
C | 1 | a0001c0001t0001g0095 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.-27+5945_-27+5954d others(12): Show |
VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr17 | 59713683 | ||||||
| chr17:59713685 | T | C | 2 | a0001c0001t0001g0231 a0001c0001t0001g0246 |
2 | HG02071.hp1 NA18982.hp2 |
intron_variant | MODIFIER | c.-27+5937T>C | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 1/11 | chr17 | 59713685 | |||||||
| chr17:59713797 | C | T | 2 | a0001c0001t0001g0255 a0001c0001t0001g0256 |
2 | HG02451.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.-27+6049C>T | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 1/11 | chr17 | 59713797 | |||||||
| chr17:59713834 | A | G | 1 | a0001c0001t0001g0092 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.-27+6086A>G | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 1/11 | chr17 | 59713834 | |||||||
| chr17:59713841 | G | A | 19 | a0001c0001t0001g0003 a0001c0001t0001g0076 a0001c0001t0001g0077 others(16): Show |
19 | HG01243.hp1 HG01891.hp2 HG02280.hp2 others(16): Show |
intron_variant | MODIFIER | c.-27+6093G>A | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 1/11 | chr17 | 59713841 | |||||||
| chr17:59714035 | C | T | 1 | a0001c0001t0001g0095 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.-27+6287C>T | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 1/11 | chr17 | 59714035 | |||||||
| chr17:59714046 | G | GA | 24 | a0001c0001t0001g0011 a0001c0001t0001g0076 a0001c0001t0001g0104 others(21): Show |
24 | HG00423.hp1 HG00438.hp1 HG00673.hp2 others(21): Show |
intron_variant | MODIFIER | c.-27+6319dupA | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr17 | 59714046 | ||||||
| chr17:59714046 | GA | G | 20 | a0001c0001t0001g0103 a0001c0001t0001g0253 a0001c0001t0001g0254 others(17): Show |
20 | HG01109.hp2 HG02109.hp2 HG02615.hp1 others(17): Show |
intron_variant | MODIFIER | c.-27+6319delA | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr17 | 59714046 | ||||||
| chr17:59714386 | C | T | 1 | a0001c0001t0006g0286 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.-27+6638C>T | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 1/11 | chr17 | 59714386 | |||||||
| chr17:59714483 | A | G | 94 | a0001c0001t0001g0100 a0001c0001t0001g0101 a0001c0001t0001g0102 others(91): Show |
94 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(91): Show |
intron_variant | MODIFIER | c.-27+6735A>G | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 1/11 | chr17 | 59714483 | |||||||
| chr17:59714582 | T | C | 1 | a0001c0001t0001g0095 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.-27+6834T>C | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 1/11 | chr17 | 59714582 | |||||||
| chr17:59714611 | C | A | 12 | a0001c0001t0003g0264 a0001c0001t0004g0262 a0001c0001t0004g0263 others(9): Show |
12 | HG01109.hp2 HG02615.hp1 HG02896.hp1 others(9): Show |
intron_variant | MODIFIER | c.-27+6863C>A | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 1/11 | chr17 | 59714611 | |||||||
| chr17:59714670 | A | G | 261 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(258): Show |
261 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(258): Show |
intron_variant | MODIFIER | c.-27+6922A>G | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 1/11 | chr17 | 59714670 | |||||||
| chr17:59715218 | C | T | 1 | a0001c0001t0004g0273 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.-27+7470C>T | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 1/11 | chr17 | 59715218 | |||||||
| chr17:59715432 | A | G | 1 | a0001c0001t0001g0095 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.-27+7684A>G | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 1/11 | chr17 | 59715432 | |||||||
| chr17:59715560 | G | A | 3 | a0001c0001t0001g0182 a0001c0001t0001g0183 a0001c0001t0001g0184 |
3 | HG02602.hp1 HG03704.hp1 HG03831.hp1 |
intron_variant | MODIFIER | c.-27+7812G>A | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 1/11 | chr17 | 59715560 | |||||||
| chr17:59715986 | T | G | 1 | a0001c0001t0002g0096 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.-27+8238T>G | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 1/11 | chr17 | 59715986 | |||||||
| chr17:59716623 | A | T | 1 | a0001c0001t0003g0257 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.-27+8875A>T | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 1/11 | chr17 | 59716623 | |||||||
| chr17:59716710 | T | G | 4 | a0001c0001t0006g0283 a0001c0001t0006g0284 a0001c0001t0006g0285 others(1): Show |
4 | HG02109.hp2 HG03130.hp2 HG06807.hp2 others(1): Show |
intron_variant | MODIFIER | c.-27+8962T>G | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 1/11 | chr17 | 59716710 | |||||||
| chr17:59716784 | A | AT | 100 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(97): Show |
100 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(97): Show |
intron_variant | MODIFIER | c.-27+9045dupT | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr17 | 59716784 | ||||||
| chr17:59716978 | A | T | 24 | a0001c0001t0001g0003 a0001c0001t0001g0076 a0001c0001t0001g0077 others(21): Show |
24 | HG01243.hp1 HG01891.hp2 HG02109.hp2 others(21): Show |
intron_variant | MODIFIER | c.-27+9230A>T | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 1/11 | chr17 | 59716978 | |||||||
| chr17:59716985 | T | A | 1 | a0001c0001t0001g0095 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.-27+9237T>A | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 1/11 | chr17 | 59716985 | |||||||
| chr17:59717192 | G | A | 1 | a0001c0001t0001g0188 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.-27+9444G>A | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 1/11 | chr17 | 59717192 | |||||||
| chr17:59717254 | G | A | 1 | a0001c0001t0014g0189 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.-27+9506G>A | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 1/11 | chr17 | 59717254 | |||||||
| chr17:59717747 | T | C | 3 | a0001c0001t0001g0100 a0001c0001t0001g0101 a0001c0001t0001g0102 |
3 | HG01261.hp2 HG01358.hp2 NA20752.hp1 |
intron_variant | MODIFIER | c.-27+9999T>C | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 1/11 | chr17 | 59717747 | |||||||
| chr17:59717904 | A | T | 1 | a0001c0001t0001g0091 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.-27+10156A>T | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 1/11 | chr17 | 59717904 | |||||||
| chr17:59718081 | G | A | 4 | a0001c0001t0003g0111 a0001c0001t0003g0112 a0001c0001t0003g0113 others(1): Show |
4 | HG00642.hp1 HG01071.hp1 HG03831.hp2 others(1): Show |
intron_variant | MODIFIER | c.-27+10333G>A | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 1/11 | chr17 | 59718081 | |||||||
| chr17:59718099 | A | T | 1 | a0001c0001t0001g0090 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.-27+10351A>T | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 1/11 | chr17 | 59718099 | |||||||
| chr17:59718122 | T | G | 50 | a0001c0001t0001g0132 a0001c0001t0001g0139 a0001c0001t0001g0277 others(47): Show |
50 | HG00438.hp2 HG00642.hp1 HG00673.hp2 others(47): Show |
intron_variant | MODIFIER | c.-27+10374T>G | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 1/11 | chr17 | 59718122 | |||||||
| chr17:59718162 | T | G | 1 | a0001c0001t0003g0114 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.-27+10414T>G | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 1/11 | chr17 | 59718162 | |||||||
| chr17:59718163 | C | A | 1 | a0001c0001t0003g0114 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.-27+10415C>A | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 1/11 | chr17 | 59718163 | |||||||
| chr17:59718184 | C | CT | 114 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(111): Show |
114 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(111): Show |
intron_variant | MODIFIER | c.-27+10464dupT | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr17 | 59718184 | ||||||
| chr17:59718184 | C | CTT | 31 | a0001c0001t0001g0010 a0001c0001t0001g0100 a0001c0001t0001g0101 others(28): Show |
31 | HG00423.hp1 HG01123.hp2 HG01256.hp2 others(28): Show |
intron_variant | MODIFIER | c.-27+10463_-27+1046 others(6): Show |
VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr17 | 59718184 | ||||||
| chr17:59718307 | C | T | 4 | a0001c0001t0003g0258 a0001c0001t0003g0259 a0001c0001t0003g0260 others(1): Show |
4 | HG02896.hp2 HG03471.hp2 NA19030.hp1 others(1): Show |
intron_variant | MODIFIER | c.-27+10559C>T | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 1/11 | chr17 | 59718307 | |||||||
| chr17:59718334 | T | C | 50 | a0001c0001t0001g0132 a0001c0001t0001g0139 a0001c0001t0001g0150 others(47): Show |
50 | HG00438.hp2 HG00642.hp1 HG00673.hp2 others(47): Show |
intron_variant | MODIFIER | c.-27+10586T>C | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 1/11 | chr17 | 59718334 | |||||||
| chr17:59718357 | C | T | 5 | a0001c0001t0003g0151 a0001c0001t0003g0258 a0001c0001t0003g0259 others(2): Show |
5 | HG02896.hp2 HG03195.hp1 HG03471.hp2 others(2): Show |
intron_variant | MODIFIER | c.-27+10609C>T | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 1/11 | chr17 | 59718357 | |||||||
| chr17:59718593 | T | A | 7 | a0001c0001t0001g0003 a0001c0001t0001g0077 a0001c0001t0001g0078 others(4): Show |
7 | HG01243.hp1 HG02258.hp2 HG02451.hp2 others(4): Show |
intron_variant | MODIFIER | c.-27+10845T>A | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 1/11 | chr17 | 59718593 | |||||||
| chr17:59718862 | A | C | 1 | a0001c0001t0001g0173 | 1 | NA18993.hp1 | intron_variant | MODIFIER | c.-27+11114A>C | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 1/11 | chr17 | 59718862 | |||||||
| chr17:59719022 | A | T | 2 | a0001c0001t0001g0069 a0001c0001t0001g0070 |
2 | NA18968.hp2 NA19056.hp2 |
intron_variant | MODIFIER | c.-27+11274A>T | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 1/11 | chr17 | 59719022 | |||||||
| chr17:59719079 | C | T | 1 | a0001c0001t0002g0074 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.-27+11331C>T | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 1/11 | chr17 | 59719079 | |||||||
| chr17:59719080 | G | A | 2 | a0001c0001t0006g0285 a0001c0001t0006g0286 |
2 | HG02109.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.-27+11332G>A | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 1/11 | chr17 | 59719080 | |||||||
| chr17:59719080 | G | T | 2 | a0001c0001t0007g0274 a0001c0001t0007g0275 |
2 | HG03491.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.-27+11332G>T | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 1/11 | chr17 | 59719080 | |||||||
| chr17:59719164 | T | C | 1 | a0001c0001t0001g0095 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.-27+11416T>C | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 1/11 | chr17 | 59719164 | |||||||
| chr17:59719284 | A | G | 1 | a0001c0001t0001g0238 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.-27+11536A>G | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 1/11 | chr17 | 59719284 | |||||||
| chr17:59719316 | C | CACAA | 97 | a0001c0001t0001g0003 a0001c0001t0001g0076 a0001c0001t0001g0077 others(94): Show |
97 | HG00408.hp2 HG00423.hp2 HG00544.hp1 others(94): Show |
intron_variant | MODIFIER | c.-27+11590_-27+1159 others(8): Show |
VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr17 | 59719316 | ||||||
| chr17:59719316 | C | CACAAACA others(1): Show |
158 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(155): Show |
158 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(155): Show |
intron_variant | MODIFIER | c.-27+11586_-27+1159 others(12): Show |
VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr17 | 59719316 | ||||||
| chr17:59719316 | C | CACAAACA others(5): Show |
2 | a0001c0001t0001g0198 a0001c0001t0003g0116 |
2 | NA18949.hp2 NA18956.hp2 |
intron_variant | MODIFIER | c.-27+11582_-27+1159 others(16): Show |
VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr17 | 59719316 | ||||||
| chr17:59719316 | C | CACAAACA others(9): Show |
1 | a0001c0001t0001g0197 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.-27+11578_-27+1159 others(20): Show |
VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr17 | 59719316 | ||||||
| chr17:59719493 | T | C | 1 | a0001c0001t0001g0199 | 1 | HG02273.hp2 | intron_variant | MODIFIER | c.-27+11745T>C | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 1/11 | chr17 | 59719493 | |||||||
| chr17:59719675 | T | G | 2 | a0001c0001t0001g0190 a0001c0001t0001g0191 |
2 | NA19001.hp1 NA19005.hp2 |
intron_variant | MODIFIER | c.-26-11746T>G | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 1/11 | chr17 | 59719675 | |||||||
| chr17:59719690 | A | G | 2 | a0001c0001t0003g0134 a0001c0001t0003g0146 |
2 | HG02895.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.-26-11731A>G | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 1/11 | chr17 | 59719690 | |||||||
| chr17:59719805 | T | C | 1 | a0001c0001t0001g0152 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.-26-11616T>C | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 1/11 | chr17 | 59719805 | |||||||
| chr17:59719849 | A | C | 2 | a0001c0001t0005g0058 a0001c0001t0005g0059 |
2 | HG02698.hp2 HG03927.hp1 |
intron_variant | MODIFIER | c.-26-11572A>C | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 1/11 | chr17 | 59719849 | |||||||
| chr17:59720026 | G | C | 2 | a0001c0001t0001g0185 a0001c0001t0001g0187 |
2 | NA18963.hp2 NA18983.hp1 |
intron_variant | MODIFIER | c.-26-11395G>C | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 1/11 | chr17 | 59720026 | |||||||
| chr17:59720804 | T | C | 161 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(158): Show |
161 | HG00408.hp2 HG00423.hp2 HG00438.hp2 others(158): Show |
intron_variant | MODIFIER | c.-26-10617T>C | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 1/11 | chr17 | 59720804 | |||||||
| chr17:59720822 | C | A | 260 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(257): Show |
260 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(257): Show |
intron_variant | MODIFIER | c.-26-10599C>A | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 1/11 | chr17 | 59720822 | |||||||
| chr17:59720871 | G | A | 11 | a0001c0001t0004g0262 a0001c0001t0004g0263 a0001c0001t0004g0265 others(8): Show |
11 | HG01109.hp2 HG02615.hp1 HG02896.hp1 others(8): Show |
intron_variant | MODIFIER | c.-26-10550G>A | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 1/11 | chr17 | 59720871 | |||||||
| chr17:59720973 | C | CA | 8 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(5): Show |
8 | HG01099.hp1 HG01884.hp1 HG01952.hp2 others(5): Show |
intron_variant | MODIFIER | c.-26-10436dupA | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr17 | 59720973 | ||||||
| chr17:59721072 | G | A | 1 | a0001c0001t0001g0200 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.-26-10349G>A | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 1/11 | chr17 | 59721072 | |||||||
| chr17:59721073 | C | T | 1 | a0001c0001t0003g0258 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.-26-10348C>T | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 1/11 | chr17 | 59721073 | |||||||
| chr17:59721100 | C | T | 2 | a0001c0001t0001g0171 a0001c0001t0001g0172 |
2 | HG01891.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.-26-10321C>T | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 1/11 | chr17 | 59721100 | |||||||
| chr17:59721333 | C | T | 2 | a0001c0001t0004g0269 a0001c0001t0004g0270 |
2 | HG03041.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.-26-10088C>T | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 1/11 | chr17 | 59721333 | |||||||
| chr17:59721715 | C | CAAACA | 98 | a0001c0001t0001g0003 a0001c0001t0001g0076 a0001c0001t0001g0077 others(95): Show |
98 | HG00408.hp2 HG00423.hp2 HG00544.hp1 others(95): Show |
intron_variant | MODIFIER | c.-26-9674_-26-9670d others(7): Show |
VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr17 | 59721715 | ||||||
| chr17:59721715 | C | CAAACAAA others(3): Show |
10 | a0001c0001t0001g0081 a0001c0001t0001g0153 a0001c0001t0002g0071 others(7): Show |
10 | HG01168.hp2 HG02027.hp2 HG02486.hp1 others(7): Show |
intron_variant | MODIFIER | c.-26-9679_-26-9670d others(12): Show |
VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr17 | 59721715 | ||||||
| chr17:59721715 | CAAACA | C | 58 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(55): Show |
58 | HG00438.hp2 HG00642.hp1 HG00673.hp2 others(55): Show |
intron_variant | MODIFIER | c.-26-9674_-26-9670d others(7): Show |
VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr17 | 59721715 | ||||||
| chr17:59721715 | CAAACAAA others(3): Show |
C | 5 | a0001c0001t0001g0252 a0001c0001t0001g0280 a0001c0001t0004g0268 others(2): Show |
5 | HG01123.hp2 HG02145.hp2 HG02818.hp1 others(2): Show |
intron_variant | MODIFIER | c.-26-9679_-26-9670d others(12): Show |
VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr17 | 59721715 | ||||||
| chr17:59721799 | T | C | 11 | a0001c0001t0001g0076 a0001c0001t0001g0081 a0001c0001t0001g0082 others(8): Show |
11 | HG01891.hp2 HG02257.hp1 HG02280.hp2 others(8): Show |
intron_variant | MODIFIER | c.-26-9622T>C | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 1/11 | chr17 | 59721799 | |||||||
| chr17:59721843 | A | G | 261 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(258): Show |
261 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(258): Show |
intron_variant | MODIFIER | c.-26-9578A>G | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 1/11 | chr17 | 59721843 | |||||||
| chr17:59722127 | A | G | 1 | a0001c0001t0001g0233 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.-26-9294A>G | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 1/11 | chr17 | 59722127 | |||||||
| chr17:59722169 | G | C | 3 | a0001c0001t0001g0280 a0001c0001t0008g0279 a0001c0001t0008g0281 |
3 | HG02145.hp2 HG02818.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.-26-9252G>C | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 1/11 | chr17 | 59722169 | |||||||
| chr17:59722467 | A | G | 1 | a0001c0001t0001g0152 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.-26-8954A>G | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 1/11 | chr17 | 59722467 | |||||||
| chr17:59722536 | A | G | 1 | a0001c0001t0004g0263 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.-26-8885A>G | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 1/11 | chr17 | 59722536 | |||||||
| chr17:59722580 | C | T | 8 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(5): Show |
8 | HG01099.hp1 HG01884.hp1 HG01952.hp2 others(5): Show |
intron_variant | MODIFIER | c.-26-8841C>T | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 1/11 | chr17 | 59722580 | |||||||
| chr17:59722613 | AGCAGAT | A | 8 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(5): Show |
8 | HG01099.hp1 HG01884.hp1 HG01952.hp2 others(5): Show |
intron_variant | MODIFIER | c.-26-8807_-26-8802d others(8): Show |
VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 1/11 | chr17 | 59722613 | |||||||
| chr17:59722620 | C | T | 8 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(5): Show |
8 | HG01099.hp1 HG01884.hp1 HG01952.hp2 others(5): Show |
intron_variant | MODIFIER | c.-26-8801C>T | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 1/11 | chr17 | 59722620 | |||||||
| chr17:59722700 | C | T | 1 | a0001c0001t0001g0251 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.-26-8721C>T | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 1/11 | chr17 | 59722700 | |||||||
| chr17:59722748 | G | T | 1 | a0001c0001t0001g0201 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.-26-8673G>T | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 1/11 | chr17 | 59722748 | |||||||
| chr17:59722938 | A | T | 1 | a0001c0001t0001g0090 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.-26-8483A>T | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 1/11 | chr17 | 59722938 | |||||||
| chr17:59722997 | C | T | 260 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(257): Show |
260 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(257): Show |
intron_variant | MODIFIER | c.-26-8424C>T | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 1/11 | chr17 | 59722997 | |||||||
| chr17:59723027 | G | A | 260 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(257): Show |
260 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(257): Show |
intron_variant | MODIFIER | c.-26-8394G>A | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 1/11 | chr17 | 59723027 | |||||||
| chr17:59723049 | T | C | 1 | a0001c0001t0001g0095 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.-26-8372T>C | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 1/11 | chr17 | 59723049 | |||||||
| chr17:59723189 | A | G | 2 | a0001c0001t0003g0259 a0001c0001t0003g0260 |
2 | HG02896.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.-26-8232A>G | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 1/11 | chr17 | 59723189 | |||||||
| chr17:59723420 | A | G | 4 | a0001c0001t0002g0016 a0001c0001t0002g0017 a0001c0001t0002g0056 others(1): Show |
4 | NA18950.hp1 NA18967.hp1 NA18983.hp2 others(1): Show |
intron_variant | MODIFIER | c.-26-8001A>G | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 1/11 | chr17 | 59723420 | |||||||
| chr17:59723605 | G | A | 78 | a0001c0001t0002g0012 a0001c0001t0002g0013 a0001c0001t0002g0014 others(75): Show |
78 | HG00408.hp2 HG00423.hp2 HG00544.hp1 others(75): Show |
intron_variant | MODIFIER | c.-26-7816G>A | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 1/11 | chr17 | 59723605 | |||||||
| chr17:59723611 | T | C | 1 | a0001c0001t0001g0238 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.-26-7810T>C | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 1/11 | chr17 | 59723611 | |||||||
| chr17:59723747 | C | T | 1 | a0001c0001t0003g0128 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.-26-7674C>T | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 1/11 | chr17 | 59723747 | |||||||
| chr17:59724061 | A | C | 100 | a0001c0001t0001g0003 a0001c0001t0001g0076 a0001c0001t0001g0077 others(97): Show |
100 | HG00408.hp2 HG00423.hp2 HG00544.hp1 others(97): Show |
intron_variant | MODIFIER | c.-26-7360A>C | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 1/11 | chr17 | 59724061 | |||||||
| chr17:59724127 | A | G | 51 | a0001c0001t0001g0132 a0001c0001t0001g0139 a0001c0001t0001g0150 others(48): Show |
51 | HG00438.hp2 HG00642.hp1 HG00673.hp2 others(48): Show |
intron_variant | MODIFIER | c.-26-7294A>G | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 1/11 | chr17 | 59724127 | |||||||
| chr17:59724211 | C | CA | 15 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(12): Show |
15 | HG01099.hp1 HG01884.hp1 HG01884.hp2 others(12): Show |
intron_variant | MODIFIER | c.-26-7195dupA | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr17 | 59724211 | ||||||
| chr17:59724224 | AAAG | A | 47 | a0001c0001t0001g0132 a0001c0001t0001g0139 a0001c0001t0001g0277 others(44): Show |
47 | HG00438.hp2 HG00642.hp1 HG00673.hp2 others(44): Show |
intron_variant | MODIFIER | c.-26-7194_-26-7192d others(5): Show |
VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr17 | 59724224 | ||||||
| chr17:59724236 | G | T | 87 | a0001c0001t0001g0069 a0001c0001t0001g0070 a0001c0001t0001g0100 others(84): Show |
87 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(84): Show |
intron_variant | MODIFIER | c.-26-7185G>T | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 1/11 | chr17 | 59724236 | |||||||
| chr17:59724380 | T | C | 2 | a0001c0001t0001g0088 a0001c0001t0001g0090 |
2 | HG02622.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.-26-7041T>C | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 1/11 | chr17 | 59724380 | |||||||
| chr17:59724400 | G | A | 87 | a0001c0001t0001g0069 a0001c0001t0001g0070 a0001c0001t0001g0100 others(84): Show |
87 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(84): Show |
intron_variant | MODIFIER | c.-26-7021G>A | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 1/11 | chr17 | 59724400 | |||||||
| chr17:59724516 | A | C | 21 | a0001c0001t0001g0003 a0001c0001t0001g0076 a0001c0001t0001g0077 others(18): Show |
21 | HG01243.hp1 HG01891.hp2 HG02257.hp1 others(18): Show |
intron_variant | MODIFIER | c.-26-6905A>C | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 1/11 | chr17 | 59724516 | |||||||
| chr17:59724596 | C | T | 1 | a0001c0001t0001g0256 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.-26-6825C>T | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 1/11 | chr17 | 59724596 | |||||||
| chr17:59724686 | G | T | 161 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(158): Show |
161 | HG00408.hp2 HG00423.hp2 HG00438.hp2 others(158): Show |
intron_variant | MODIFIER | c.-26-6735G>T | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 1/11 | chr17 | 59724686 | |||||||
| chr17:59724735 | G | A | 1 | a0001c0001t0004g0271 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.-26-6686G>A | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 1/11 | chr17 | 59724735 | |||||||
| chr17:59724791 | A | C | 173 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(170): Show |
173 | HG00408.hp2 HG00423.hp2 HG00438.hp2 others(170): Show |
intron_variant | MODIFIER | c.-26-6630A>C | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 1/11 | chr17 | 59724791 | |||||||
| chr17:59724823 | G | A | 1 | a0001c0001t0003g0148 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.-26-6598G>A | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 1/11 | chr17 | 59724823 | |||||||
| chr17:59724965 | CA | C | 173 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(170): Show |
173 | HG00408.hp2 HG00423.hp2 HG00438.hp2 others(170): Show |
intron_variant | MODIFIER | c.-26-6445delA | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr17 | 59724965 | ||||||
| chr17:59724990 | C | CA | 96 | a0001c0001t0001g0003 a0001c0001t0001g0076 a0001c0001t0001g0077 others(93): Show |
96 | HG00408.hp2 HG00423.hp2 HG00544.hp1 others(93): Show |
intron_variant | MODIFIER | c.-26-6423dupA | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr17 | 59724990 | ||||||
| chr17:59725551 | C | CA | 162 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(159): Show |
162 | HG00408.hp2 HG00423.hp2 HG00438.hp2 others(159): Show |
intron_variant | MODIFIER | c.-26-5854dupA | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr17 | 59725551 | ||||||
| chr17:59725602 | A | G | 1 | a0001c0001t0002g0051 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.-26-5819A>G | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 1/11 | chr17 | 59725602 | |||||||
| chr17:59725605 | C | T | 45 | a0001c0001t0002g0014 a0001c0001t0002g0015 a0001c0001t0002g0016 others(42): Show |
45 | HG00408.hp2 HG00423.hp2 HG00544.hp1 others(42): Show |
intron_variant | MODIFIER | c.-26-5816C>T | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 1/11 | chr17 | 59725605 | |||||||
| chr17:59725635 | A | G | 1 | a0001c0001t0001g0277 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.-26-5786A>G | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 1/11 | chr17 | 59725635 | |||||||
| chr17:59725802 | A | C | 1 | a0001c0001t0001g0170 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.-26-5619A>C | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 1/11 | chr17 | 59725802 | |||||||
| chr17:59726291 | G | GT | 88 | a0001c0001t0001g0069 a0001c0001t0001g0070 a0001c0001t0001g0100 others(85): Show |
88 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(85): Show |
intron_variant | MODIFIER | c.-26-5119dupT | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr17 | 59726291 | ||||||
| chr17:59726366 | T | G | 1 | a0001c0001t0001g0238 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.-26-5055T>G | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 1/11 | chr17 | 59726366 | |||||||
| chr17:59726422 | T | G | 1 | a0001c0001t0001g0205 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.-26-4999T>G | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 1/11 | chr17 | 59726422 | |||||||
| chr17:59726514 | G | A | 1 | a0001c0001t0003g0149 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.-26-4907G>A | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 1/11 | chr17 | 59726514 | |||||||
| chr17:59726529 | G | T | 1 | a0001c0001t0001g0183 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.-26-4892G>T | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 1/11 | chr17 | 59726529 | |||||||
| chr17:59726678 | T | A | 2 | a0001c0001t0006g0283 a0001c0001t0006g0284 |
2 | HG03130.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.-26-4743T>A | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 1/11 | chr17 | 59726678 | |||||||
| chr17:59726804 | T | G | 1 | a0001c0001t0001g0277 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.-26-4617T>G | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 1/11 | chr17 | 59726804 | |||||||
| chr17:59727125 | C | A | 1 | a0001c0001t0001g0159 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.-26-4296C>A | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 1/11 | chr17 | 59727125 | |||||||
| chr17:59727125 | CTTTTTGT others(3): Show |
C | 11 | a0001c0001t0004g0262 a0001c0001t0004g0263 a0001c0001t0004g0265 others(8): Show |
11 | HG01109.hp2 HG02615.hp1 HG02896.hp1 others(8): Show |
intron_variant | MODIFIER | c.-26-4279_-26-4270d others(12): Show |
VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr17 | 59727125 | ||||||
| chr17:59727558 | A | T | 1 | a0001c0001t0001g0184 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.-26-3863A>T | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 1/11 | chr17 | 59727558 | |||||||
| chr17:59727775 | C | G | 1 | a0001c0001t0001g0178 | 1 | NA19080.hp1 | intron_variant | MODIFIER | c.-26-3646C>G | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 1/11 | chr17 | 59727775 | |||||||
| chr17:59727872 | G | T | 1 | a0001c0001t0001g0158 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.-26-3549G>T | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 1/11 | chr17 | 59727872 | |||||||
| chr17:59727889 | G | A | 1 | a0001c0001t0001g0077 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.-26-3532G>A | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 1/11 | chr17 | 59727889 | |||||||
| chr17:59728020 | T | C | 1 | a0001c0001t0001g0095 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.-26-3401T>C | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 1/11 | chr17 | 59728020 | |||||||
| chr17:59728159 | G | C | 281 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(278): Show |
281 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(278): Show |
intron_variant | MODIFIER | c.-26-3262G>C | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 1/11 | chr17 | 59728159 | |||||||
| chr17:59728318 | T | C | 1 | a0001c0001t0001g0198 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.-26-3103T>C | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 1/11 | chr17 | 59728318 | |||||||
| chr17:59728366 | A | G | 2 | a0001c0001t0001g0008 a0001c0001t0001g0009 |
2 | HG01884.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.-26-3055A>G | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 1/11 | chr17 | 59728366 | |||||||
| chr17:59728439 | C | CAT | 11 | a0001c0001t0004g0262 a0001c0001t0004g0263 a0001c0001t0004g0265 others(8): Show |
11 | HG01109.hp2 HG02615.hp1 HG02896.hp1 others(8): Show |
intron_variant | MODIFIER | c.-26-2977_-26-2976d others(4): Show |
VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr17 | 59728439 | ||||||
| chr17:59728544 | A | G | 1 | a0001c0001t0001g0088 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.-26-2877A>G | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 1/11 | chr17 | 59728544 | |||||||
| chr17:59728650 | G | T | 78 | a0001c0001t0002g0012 a0001c0001t0002g0013 a0001c0001t0002g0014 others(75): Show |
78 | HG00408.hp2 HG00423.hp2 HG00544.hp1 others(75): Show |
intron_variant | MODIFIER | c.-26-2771G>T | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 1/11 | chr17 | 59728650 | |||||||
| chr17:59728684 | A | ATTAT | 58 | a0001c0001t0001g0132 a0001c0001t0001g0139 a0001c0001t0003g0105 others(55): Show |
58 | HG00438.hp2 HG00642.hp1 HG00673.hp2 others(55): Show |
intron_variant | MODIFIER | c.-26-2716_-26-2713d others(6): Show |
VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr17 | 59728684 | ||||||
| chr17:59728876 | A | G | 1 | a0001c0001t0004g0273 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.-26-2545A>G | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 1/11 | chr17 | 59728876 | |||||||
| chr17:59729197 | G | A | 1 | a0001c0001t0003g0257 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.-26-2224G>A | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 1/11 | chr17 | 59729197 | |||||||
| chr17:59729279 | A | T | 260 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(257): Show |
260 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(257): Show |
intron_variant | MODIFIER | c.-26-2142A>T | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 1/11 | chr17 | 59729279 | |||||||
| chr17:59729318 | A | G | 1 | a0001c0001t0005g0002 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.-26-2103A>G | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 1/11 | chr17 | 59729318 | |||||||
| chr17:59729408 | G | A | 1 | a0001c0001t0001g0166 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.-26-2013G>A | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 1/11 | chr17 | 59729408 | |||||||
| chr17:59729478 | C | CA | 26 | a0001c0001t0001g0078 a0001c0001t0001g0088 a0001c0001t0001g0103 others(23): Show |
26 | HG00438.hp2 HG00621.hp2 HG00738.hp1 others(23): Show |
intron_variant | MODIFIER | c.-26-1924dupA | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr17 | 59729478 | ||||||
| chr17:59729491 | A | C | 7 | a0001c0001t0001g0200 a0001c0001t0001g0231 a0001c0001t0001g0232 others(4): Show |
7 | NA18942.hp2 NA18943.hp2 NA18959.hp1 others(4): Show |
intron_variant | MODIFIER | c.-26-1930A>C | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 1/11 | chr17 | 59729491 | |||||||
| chr17:59729673 | C | A | 11 | a0001c0001t0004g0262 a0001c0001t0004g0263 a0001c0001t0004g0265 others(8): Show |
11 | HG01109.hp2 HG02615.hp1 HG02896.hp1 others(8): Show |
intron_variant | MODIFIER | c.-26-1748C>A | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 1/11 | chr17 | 59729673 | |||||||
| chr17:59729686 | C | CT | 104 | a0001c0001t0001g0003 a0001c0001t0001g0076 a0001c0001t0001g0077 others(101): Show |
104 | HG00408.hp1 HG00408.hp2 HG00423.hp2 others(101): Show |
intron_variant | MODIFIER | c.-26-1719dupT | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr17 | 59729686 | ||||||
| chr17:59729738 | C | T | 1 | a0001c0001t0001g0277 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.-26-1683C>T | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 1/11 | chr17 | 59729738 | |||||||
| chr17:59729790 | A | T | 3 | a0001c0001t0001g0188 a0001c0001t0001g0230 a0001c0001t0001g0249 |
3 | HG01074.hp2 HG01361.hp2 HG02280.hp1 |
intron_variant | MODIFIER | c.-26-1631A>T | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 1/11 | chr17 | 59729790 | |||||||
| chr17:59729795 | C | T | 1 | a0001c0001t0002g0019 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.-26-1626C>T | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 1/11 | chr17 | 59729795 | |||||||
| chr17:59729810 | C | T | 2 | a0001c0001t0001g0078 a0001c0001t0001g0080 |
2 | HG01243.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.-26-1611C>T | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 1/11 | chr17 | 59729810 | |||||||
| chr17:59730131 | G | A | 1 | a0001c0001t0001g0207 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.-26-1290G>A | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 1/11 | chr17 | 59730131 | |||||||
| chr17:59730259 | A | G | 2 | a0001c0001t0004g0265 a0001c0001t0004g0266 |
2 | HG02970.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.-26-1162A>G | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 1/11 | chr17 | 59730259 | |||||||
| chr17:59731244 | G | A | 1 | a0001c0001t0003g0137 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.-26-177G>A | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 1/11 | chr17 | 59731244 | |||||||
| chr17:59731249 | A | G | 1 | a0001c0001t0006g0284 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.-26-172A>G | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 1/11 | chr17 | 59731249 | |||||||
| chr17:59731555 | A | T | 1 | a0001c0001t0001g0090 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.76+33A>T | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 2/11 | chr17 | 59731555 | |||||||
| chr17:59732092 | A | T | 260 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(257): Show |
260 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(257): Show |
intron_variant | MODIFIER | c.76+570A>T | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 2/11 | chr17 | 59732092 | |||||||
| chr17:59732104 | A | G | 1 | a0001c0001t0003g0127 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.76+582A>G | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 2/11 | chr17 | 59732104 | |||||||
| chr17:59732154 | C | A | 1 | a0001c0001t0005g0061 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.76+632C>A | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 2/11 | chr17 | 59732154 | |||||||
| chr17:59732269 | C | T | 1 | a0001c0001t0003g0156 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.76+747C>T | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 2/11 | chr17 | 59732269 | |||||||
| chr17:59732392 | G | A | 1 | a0001c0001t0001g0200 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.76+870G>A | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 2/11 | chr17 | 59732392 | |||||||
| chr17:59732492 | C | T | 1 | a0001c0001t0001g0095 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.76+970C>T | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 2/11 | chr17 | 59732492 | |||||||
| chr17:59732532 | C | T | 2 | a0001c0001t0007g0274 a0001c0001t0007g0275 |
2 | HG03491.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.76+1010C>T | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 2/11 | chr17 | 59732532 | |||||||
| chr17:59732534 | C | T | 8 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(5): Show |
8 | HG01099.hp1 HG01884.hp1 HG01952.hp2 others(5): Show |
intron_variant | MODIFIER | c.76+1012C>T | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 2/11 | chr17 | 59732534 | |||||||
| chr17:59732552 | TGTTA | T | 87 | a0001c0001t0001g0069 a0001c0001t0001g0070 a0001c0001t0001g0100 others(84): Show |
87 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(84): Show |
intron_variant | MODIFIER | c.76+1031_76+1034del others(4): Show |
VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 2/11 | chr17 | 59732552 | |||||||
| chr17:59732673 | T | C | 1 | a0001c0001t0001g0277 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.76+1151T>C | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 2/11 | chr17 | 59732673 | |||||||
| chr17:59732795 | A | G | 2 | a0001c0001t0001g0081 a0001c0001t0001g0092 |
2 | HG02622.hp2 HG02647.hp2 |
intron_variant | MODIFIER | c.76+1273A>G | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 2/11 | chr17 | 59732795 | |||||||
| chr17:59732809 | A | G | 1 | a0001c0001t0001g0277 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.76+1287A>G | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 2/11 | chr17 | 59732809 | |||||||
| chr17:59733188 | A | C | 53 | a0001c0001t0001g0132 a0001c0001t0001g0139 a0001c0001t0001g0203 others(50): Show |
53 | HG00438.hp2 HG00544.hp1 HG00642.hp1 others(50): Show |
intron_variant | MODIFIER | c.76+1666A>C | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 2/11 | chr17 | 59733188 | |||||||
| chr17:59733189 | A | C | 1 | a0001c0001t0003g0114 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.76+1667A>C | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 2/11 | chr17 | 59733189 | |||||||
| chr17:59733199 | T | A | 1 | a0001c0001t0001g0251 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.76+1677T>A | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 2/11 | chr17 | 59733199 | |||||||
| chr17:59733284 | A | G | 3 | a0001c0001t0001g0161 a0001c0001t0001g0162 a0001c0001t0001g0163 |
3 | HG01255.hp1 HG01256.hp1 HG01258.hp2 |
intron_variant | MODIFIER | c.76+1762A>G | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 2/11 | chr17 | 59733284 | |||||||
| chr17:59733472 | T | TG | 5 | a0001c0001t0004g0262 a0001c0001t0004g0263 a0001c0001t0004g0267 others(2): Show |
5 | HG01109.hp2 HG02896.hp1 HG03486.hp2 others(2): Show |
intron_variant | MODIFIER | c.77-1864dupG | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr17 | 59733472 | ||||||
| chr17:59733524 | C | G | 1 | a0001c0001t0001g0229 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.77-1814C>G | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 2/11 | chr17 | 59733524 | |||||||
| chr17:59733620 | T | A | 1 | a0001c0001t0003g0134 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.77-1718T>A | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 2/11 | chr17 | 59733620 | |||||||
| chr17:59734046 | A | C | 103 | a0001c0001t0001g0003 a0001c0001t0001g0076 a0001c0001t0001g0077 others(100): Show |
103 | HG00408.hp2 HG00423.hp2 HG00544.hp1 others(100): Show |
intron_variant | MODIFIER | c.77-1292A>C | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 2/11 | chr17 | 59734046 | |||||||
| chr17:59734246 | AG | A | 11 | a0001c0001t0004g0262 a0001c0001t0004g0263 a0001c0001t0004g0265 others(8): Show |
11 | HG01109.hp2 HG02615.hp1 HG02896.hp1 others(8): Show |
intron_variant | MODIFIER | c.77-1091delG | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 2/11 | chr17 | 59734246 | |||||||
| chr17:59734448 | G | A | 1 | a0001c0001t0001g0095 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.77-890G>A | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 2/11 | chr17 | 59734448 | |||||||
| chr17:59734706 | T | C | 104 | a0001c0001t0001g0003 a0001c0001t0001g0076 a0001c0001t0001g0077 others(101): Show |
104 | HG00408.hp2 HG00423.hp2 HG00544.hp1 others(101): Show |
intron_variant | MODIFIER | c.77-632T>C | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 2/11 | chr17 | 59734706 | |||||||
| chr17:59734772 | T | C | 1 | a0001c0001t0001g0178 | 1 | NA19080.hp1 | intron_variant | MODIFIER | c.77-566T>C | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 2/11 | chr17 | 59734772 | |||||||
| chr17:59734902 | C | CT | 81 | a0001c0001t0001g0010 a0001c0001t0001g0069 a0001c0001t0001g0070 others(78): Show |
81 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(78): Show |
intron_variant | MODIFIER | c.77-413dupT | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr17 | 59734902 | ||||||
| chr17:59734902 | C | CTT | 94 | a0001c0001t0001g0076 a0001c0001t0001g0081 a0001c0001t0001g0082 others(91): Show |
94 | HG00408.hp2 HG00423.hp2 HG00544.hp1 others(91): Show |
intron_variant | MODIFIER | c.77-414_77-413dupTT | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr17 | 59734902 | ||||||
| chr17:59734902 | C | CTTT | 17 | a0001c0001t0001g0003 a0001c0001t0001g0077 a0001c0001t0001g0079 others(14): Show |
17 | HG00673.hp1 HG00741.hp1 HG01358.hp1 others(14): Show |
intron_variant | MODIFIER | c.77-415_77-413dupTT others(1): Show |
VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr17 | 59734902 | ||||||
| chr17:59735013 | G | A | 11 | a0001c0001t0004g0262 a0001c0001t0004g0263 a0001c0001t0004g0265 others(8): Show |
11 | HG01109.hp2 HG02615.hp1 HG02896.hp1 others(8): Show |
intron_variant | MODIFIER | c.77-325G>A | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 2/11 | chr17 | 59735013 | |||||||
| chr17:59735574 | G | T | 1 | a0001c0001t0001g0241 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.212+101G>T | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 3/11 | chr17 | 59735574 | |||||||
| chr17:59735807 | A | G | 58 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(55): Show |
58 | HG00438.hp2 HG00642.hp1 HG00673.hp2 others(55): Show |
intron_variant | MODIFIER | c.212+334A>G | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 3/11 | chr17 | 59735807 | |||||||
| chr17:59736323 | A | C | 1 | a0001c0001t0010g0228 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.212+850A>C | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 3/11 | chr17 | 59736323 | |||||||
| chr17:59736402 | CA | C | 270 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(267): Show |
270 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(267): Show |
intron_variant | MODIFIER | c.212+943delA | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr17 | 59736402 | ||||||
| chr17:59736463 | A | G | 260 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(257): Show |
260 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(257): Show |
intron_variant | MODIFIER | c.212+990A>G | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 3/11 | chr17 | 59736463 | |||||||
| chr17:59736765 | G | A | 2 | a0001c0001t0002g0074 a0001c0001t0002g0075 |
2 | HG01981.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.213-688G>A | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 3/11 | chr17 | 59736765 | |||||||
| chr17:59737067 | T | C | 21 | a0001c0001t0001g0003 a0001c0001t0001g0076 a0001c0001t0001g0077 others(18): Show |
21 | HG01243.hp1 HG01891.hp2 HG02257.hp1 others(18): Show |
intron_variant | MODIFIER | c.213-386T>C | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 3/11 | chr17 | 59737067 | |||||||
| chr17:59737280 | A | G | 78 | a0001c0001t0002g0012 a0001c0001t0002g0013 a0001c0001t0002g0014 others(75): Show |
78 | HG00408.hp2 HG00423.hp2 HG00544.hp1 others(75): Show |
intron_variant | MODIFIER | c.213-173A>G | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 3/11 | chr17 | 59737280 | |||||||
| chr17:59737335 | A | C | 2 | a0001c0002t0001g0226 a0001c0002t0001g0227 |
2 | HG00140.hp2 HG00544.hp2 |
intron_variant | MODIFIER | c.213-118A>C | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 3/11 | chr17 | 59737335 | |||||||
| chr17:59737579 | C | G | 1 | a0001c0001t0003g0116 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.303+36C>G | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 4/11 | chr17 | 59737579 | |||||||
| chr17:59738060 | C | T | 2 | a0001c0001t0007g0274 a0001c0001t0007g0275 |
2 | HG03491.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.303+517C>T | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 4/11 | chr17 | 59738060 | |||||||
| chr17:59738102 | G | A | 1 | a0001c0001t0002g0071 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.303+559G>A | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 4/11 | chr17 | 59738102 | |||||||
| chr17:59738247 | G | C | 87 | a0001c0001t0001g0069 a0001c0001t0001g0070 a0001c0001t0001g0100 others(84): Show |
87 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(84): Show |
intron_variant | MODIFIER | c.304-590G>C | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 4/11 | chr17 | 59738247 | |||||||
| chr17:59739217 | T | C | 102 | a0001c0001t0001g0003 a0001c0001t0001g0076 a0001c0001t0001g0077 others(99): Show |
102 | HG00408.hp2 HG00423.hp2 HG00544.hp1 others(99): Show |
intron_variant | MODIFIER | c.414+270T>C | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 5/11 | chr17 | 59739217 | |||||||
| chr17:59739309 | A | G | 1 | a0001c0001t0001g0095 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.414+362A>G | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 5/11 | chr17 | 59739309 | |||||||
| chr17:59739396 | T | C | 89 | a0001c0001t0001g0069 a0001c0001t0001g0070 a0001c0001t0001g0100 others(86): Show |
89 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(86): Show |
intron_variant | MODIFIER | c.414+449T>C | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 5/11 | chr17 | 59739396 | |||||||
| chr17:59739478 | A | G | 1 | a0002c0003t0002g0030 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.414+531A>G | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 5/11 | chr17 | 59739478 | |||||||
| chr17:59739581 | G | A | 1 | a0001c0001t0001g0242 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.414+634G>A | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 5/11 | chr17 | 59739581 | |||||||
| chr17:59739655 | C | T | 1 | a0001c0001t0001g0095 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.414+708C>T | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 5/11 | chr17 | 59739655 | |||||||
| chr17:59739723 | C | CA | 10 | a0001c0001t0004g0262 a0001c0001t0004g0263 a0001c0001t0004g0265 others(7): Show |
10 | HG01109.hp2 HG02615.hp1 HG02965.hp2 others(7): Show |
intron_variant | MODIFIER | c.414+798dupA | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr17 | 59739723 | ||||||
| chr17:59739723 | CA | C | 239 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(236): Show |
239 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(236): Show |
intron_variant | MODIFIER | c.414+798delA | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr17 | 59739723 | ||||||
| chr17:59739801 | T | C | 260 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(257): Show |
260 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(257): Show |
intron_variant | MODIFIER | c.414+854T>C | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 5/11 | chr17 | 59739801 | |||||||
| chr17:59739833 | T | C | 2 | a0001c0001t0001g0077 a0001c0001t0001g0278 |
2 | HG02258.hp2 HG02630.hp1 |
intron_variant | MODIFIER | c.414+886T>C | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 5/11 | chr17 | 59739833 | |||||||
| chr17:59740019 | G | A | 1 | a0001c0001t0001g0158 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.414+1072G>A | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 5/11 | chr17 | 59740019 | |||||||
| chr17:59740076 | CA | C | 11 | a0001c0001t0004g0262 a0001c0001t0004g0263 a0001c0001t0004g0265 others(8): Show |
11 | HG01109.hp2 HG02615.hp1 HG02896.hp1 others(8): Show |
intron_variant | MODIFIER | c.414+1142delA | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr17 | 59740076 | ||||||
| chr17:59740312 | G | A | 1 | a0001c0001t0002g0236 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.414+1365G>A | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 5/11 | chr17 | 59740312 | |||||||
| chr17:59740336 | A | G | 1 | a0001c0001t0001g0199 | 1 | HG02273.hp2 | intron_variant | MODIFIER | c.414+1389A>G | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 5/11 | chr17 | 59740336 | |||||||
| chr17:59740450 | C | T | 10 | a0001c0001t0003g0107 a0001c0001t0003g0108 a0001c0001t0003g0133 others(7): Show |
10 | HG00438.hp2 HG02071.hp2 HG03927.hp2 others(7): Show |
intron_variant | MODIFIER | c.414+1503C>T | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 5/11 | chr17 | 59740450 | |||||||
| chr17:59740793 | G | A | 7 | a0001c0001t0001g0201 a0001c0001t0001g0204 a0001c0001t0001g0208 others(4): Show |
7 | HG02145.hp2 HG02818.hp1 HG02886.hp1 others(4): Show |
intron_variant | MODIFIER | c.414+1846G>A | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 5/11 | chr17 | 59740793 | |||||||
| chr17:59740852 | A | G | 52 | a0001c0001t0001g0087 a0001c0001t0001g0132 a0001c0001t0001g0139 others(49): Show |
52 | HG00438.hp2 HG00642.hp1 HG00673.hp2 others(49): Show |
intron_variant | MODIFIER | c.414+1905A>G | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 5/11 | chr17 | 59740852 | |||||||
| chr17:59740980 | T | C | 1 | a0001c0001t0003g0138 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.414+2033T>C | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 5/11 | chr17 | 59740980 | |||||||
| chr17:59741206 | T | A | 1 | a0001c0001t0002g0098 | 1 | NA18992.hp1 | intron_variant | MODIFIER | c.414+2259T>A | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 5/11 | chr17 | 59741206 | |||||||
| chr17:59741207 | A | T | 1 | a0001c0001t0002g0098 | 1 | NA18992.hp1 | intron_variant | MODIFIER | c.414+2260A>T | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 5/11 | chr17 | 59741207 | |||||||
| chr17:59741345 | A | G | 11 | a0001c0001t0004g0262 a0001c0001t0004g0263 a0001c0001t0004g0265 others(8): Show |
11 | HG01109.hp2 HG02615.hp1 HG02896.hp1 others(8): Show |
intron_variant | MODIFIER | c.414+2398A>G | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 5/11 | chr17 | 59741345 | |||||||
| chr17:59741532 | C | G | 1 | a0001c0001t0002g0034 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.414+2585C>G | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 5/11 | chr17 | 59741532 | |||||||
| chr17:59741621 | G | T | 1 | a0001c0001t0003g0113 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.414+2674G>T | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 5/11 | chr17 | 59741621 | |||||||
| chr17:59741742 | C | G | 1 | a0001c0001t0001g0240 | 1 | NA18975.hp1 | intron_variant | MODIFIER | c.414+2795C>G | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 5/11 | chr17 | 59741742 | |||||||
| chr17:59742428 | G | A | 1 | a0001c0001t0003g0141 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.414+3481G>A | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 5/11 | chr17 | 59742428 | |||||||
| chr17:59742477 | A | C | 1 | a0001c0001t0003g0105 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.414+3530A>C | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 5/11 | chr17 | 59742477 | |||||||
| chr17:59742488 | A | G | 269 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(266): Show |
269 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(266): Show |
intron_variant | MODIFIER | c.414+3541A>G | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 5/11 | chr17 | 59742488 | |||||||
| chr17:59742522 | C | CAAT | 25 | a0001c0001t0001g0080 a0001c0001t0001g0091 a0001c0001t0001g0166 others(22): Show |
25 | HG00423.hp2 HG01109.hp2 HG01361.hp2 others(22): Show |
intron_variant | MODIFIER | c.414+3607_414+3609d others(5): Show |
VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr17 | 59742522 | ||||||
| chr17:59742522 | C | CAATAAT | 13 | a0001c0001t0001g0070 a0001c0001t0001g0176 a0001c0001t0001g0197 others(10): Show |
13 | HG01243.hp2 HG01884.hp2 HG01978.hp2 others(10): Show |
intron_variant | MODIFIER | c.414+3604_414+3609d others(8): Show |
VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr17 | 59742522 | ||||||
| chr17:59742522 | C | CAATAATA others(2): Show |
67 | a0001c0001t0001g0069 a0001c0001t0001g0100 a0001c0001t0001g0101 others(64): Show |
67 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(64): Show |
intron_variant | MODIFIER | c.414+3601_414+3609d others(11): Show |
VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr17 | 59742522 | ||||||
| chr17:59742522 | C | CAATAATA others(5): Show |
1 | a0001c0001t0001g0209 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.414+3598_414+3609d others(14): Show |
VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr17 | 59742522 | ||||||
| chr17:59742522 | CAAT | C | 58 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(55): Show |
58 | HG00438.hp2 HG00642.hp1 HG00673.hp2 others(55): Show |
intron_variant | MODIFIER | c.414+3607_414+3609d others(5): Show |
VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr17 | 59742522 | ||||||
| chr17:59742688 | G | A | 1 | a0001c0001t0001g0089 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.414+3741G>A | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 5/11 | chr17 | 59742688 | |||||||
| chr17:59742871 | A | C | 1 | a0001c0001t0001g0222 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.414+3924A>C | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 5/11 | chr17 | 59742871 | |||||||
| chr17:59742995 | G | A | 50 | a0001c0001t0001g0132 a0001c0001t0001g0139 a0001c0001t0001g0277 others(47): Show |
50 | HG00438.hp2 HG00642.hp1 HG00673.hp2 others(47): Show |
intron_variant | MODIFIER | c.414+4048G>A | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 5/11 | chr17 | 59742995 | |||||||
| chr17:59743011 | A | G | 1 | a0001c0001t0001g0201 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.414+4064A>G | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 5/11 | chr17 | 59743011 | |||||||
| chr17:59743082 | A | G | 1 | a0001c0001t0001g0010 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.414+4135A>G | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 5/11 | chr17 | 59743082 | |||||||
| chr17:59743373 | C | T | 1 | a0001c0001t0001g0221 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.414+4426C>T | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 5/11 | chr17 | 59743373 | |||||||
| chr17:59743537 | T | G | 1 | a0001c0001t0003g0118 | 1 | NA19086.hp2 | intron_variant | MODIFIER | c.414+4590T>G | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 5/11 | chr17 | 59743537 | |||||||
| chr17:59743559 | GCTCTCTC others(3): Show |
G | 4 | a0001c0001t0003g0111 a0001c0001t0003g0112 a0001c0001t0003g0113 others(1): Show |
4 | HG00642.hp1 HG01071.hp1 HG03831.hp2 others(1): Show |
intron_variant | MODIFIER | c.414+4625_414+4634d others(12): Show |
VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr17 | 59743559 | ||||||
| chr17:59743576 | C | A | 1 | a0001c0001t0001g0277 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.414+4629C>A | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 5/11 | chr17 | 59743576 | |||||||
| chr17:59743578 | C | A | 8 | a0001c0001t0001g0088 a0001c0001t0001g0090 a0001c0001t0001g0104 others(5): Show |
8 | HG01123.hp2 HG01361.hp1 HG02109.hp2 others(5): Show |
intron_variant | MODIFIER | c.414+4631C>A | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 5/11 | chr17 | 59743578 | |||||||
| chr17:59743580 | C | A | 43 | a0001c0001t0001g0088 a0001c0001t0001g0089 a0001c0001t0001g0090 others(40): Show |
43 | HG00408.hp1 HG00438.hp1 HG00738.hp1 others(40): Show |
intron_variant | MODIFIER | c.414+4633C>A | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 5/11 | chr17 | 59743580 | |||||||
| chr17:59743582 | A | C | 44 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(41): Show |
44 | HG00408.hp2 HG01099.hp1 HG01884.hp1 others(41): Show |
intron_variant | MODIFIER | c.414+4635A>C | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 5/11 | chr17 | 59743582 | |||||||
| chr17:59743941 | G | T | 1 | a0001c0001t0001g0153 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.414+4994G>T | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 5/11 | chr17 | 59743941 | |||||||
| chr17:59744069 | G | A | 173 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(170): Show |
173 | HG00408.hp2 HG00423.hp2 HG00438.hp2 others(170): Show |
intron_variant | MODIFIER | c.414+5122G>A | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 5/11 | chr17 | 59744069 | |||||||
| chr17:59744092 | G | GT | 104 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0076 others(101): Show |
104 | HG00408.hp2 HG00423.hp2 HG00544.hp1 others(101): Show |
intron_variant | MODIFIER | c.414+5157dupT | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr17 | 59744092 | ||||||
| chr17:59744092 | G | T | 2 | a0001c0001t0001g0077 a0001c0001t0001g0086 |
2 | HG02280.hp2 HG02630.hp1 |
intron_variant | MODIFIER | c.414+5145G>T | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 5/11 | chr17 | 59744092 | |||||||
| chr17:59744322 | C | T | 1 | a0001c0001t0003g0143 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.414+5375C>T | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 5/11 | chr17 | 59744322 | |||||||
| chr17:59744330 | C | A | 1 | a0001c0001t0001g0183 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.414+5383C>A | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 5/11 | chr17 | 59744330 | |||||||
| chr17:59744462 | C | CA | 20 | a0001c0001t0001g0205 a0001c0001t0001g0229 a0001c0001t0001g0243 others(17): Show |
20 | HG01109.hp2 HG01243.hp2 HG01358.hp1 others(17): Show |
intron_variant | MODIFIER | c.414+5536dupA | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr17 | 59744462 | ||||||
| chr17:59744462 | CA | C | 17 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0087 others(14): Show |
17 | HG01884.hp1 HG02257.hp2 HG02647.hp1 others(14): Show |
intron_variant | MODIFIER | c.414+5536delA | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr17 | 59744462 | ||||||
| chr17:59744462 | CAA | C | 37 | a0001c0001t0001g0132 a0001c0001t0001g0139 a0001c0001t0003g0107 others(34): Show |
37 | HG00438.hp2 HG00642.hp1 HG00673.hp2 others(34): Show |
intron_variant | MODIFIER | c.414+5535_414+5536d others(4): Show |
VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr17 | 59744462 | ||||||
| chr17:59744764 | C | T | 104 | a0001c0001t0001g0003 a0001c0001t0001g0076 a0001c0001t0001g0077 others(101): Show |
104 | HG00408.hp2 HG00423.hp2 HG00544.hp1 others(101): Show |
intron_variant | MODIFIER | c.414+5817C>T | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 5/11 | chr17 | 59744764 | |||||||
| chr17:59744771 | A | G | 4 | a0001c0001t0001g0175 a0001c0001t0001g0220 a0001c0001t0001g0225 others(1): Show |
4 | HG00642.hp2 HG01978.hp2 HG01981.hp1 others(1): Show |
intron_variant | MODIFIER | c.414+5824A>G | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 5/11 | chr17 | 59744771 | |||||||
| chr17:59744993 | A | G | 104 | a0001c0001t0001g0003 a0001c0001t0001g0076 a0001c0001t0001g0077 others(101): Show |
104 | HG00408.hp2 HG00423.hp2 HG00544.hp1 others(101): Show |
intron_variant | MODIFIER | c.414+6046A>G | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 5/11 | chr17 | 59744993 | |||||||
| chr17:59745017 | G | T | 1 | a0001c0001t0001g0238 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.414+6070G>T | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 5/11 | chr17 | 59745017 | |||||||
| chr17:59745247 | G | T | 58 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(55): Show |
58 | HG00438.hp2 HG00642.hp1 HG00673.hp2 others(55): Show |
intron_variant | MODIFIER | c.414+6300G>T | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 5/11 | chr17 | 59745247 | |||||||
| chr17:59745386 | G | A | 4 | a0001c0001t0002g0024 a0001c0001t0002g0025 a0001c0001t0002g0026 others(1): Show |
4 | NA19057.hp2 NA19060.hp1 NA19084.hp1 others(1): Show |
intron_variant | MODIFIER | c.414+6439G>A | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 5/11 | chr17 | 59745386 | |||||||
| chr17:59745533 | A | T | 1 | a0001c0001t0001g0183 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.414+6586A>T | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 5/11 | chr17 | 59745533 | |||||||
| chr17:59745552 | T | G | 2 | a0001c0001t0007g0274 a0001c0001t0007g0275 |
2 | HG03491.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.414+6605T>G | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 5/11 | chr17 | 59745552 | |||||||
| chr17:59746192 | A | T | 11 | a0001c0001t0004g0262 a0001c0001t0004g0263 a0001c0001t0004g0265 others(8): Show |
11 | HG01109.hp2 HG02615.hp1 HG02896.hp1 others(8): Show |
intron_variant | MODIFIER | c.414+7245A>T | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 5/11 | chr17 | 59746192 | |||||||
| chr17:59746324 | G | A | 173 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(170): Show |
173 | HG00408.hp2 HG00423.hp2 HG00438.hp2 others(170): Show |
intron_variant | MODIFIER | c.414+7377G>A | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 5/11 | chr17 | 59746324 | |||||||
| chr17:59746401 | G | A | 1 | a0001c0001t0001g0081 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.414+7454G>A | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 5/11 | chr17 | 59746401 | |||||||
| chr17:59746418 | C | T | 1 | a0001c0001t0001g0254 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.414+7471C>T | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 5/11 | chr17 | 59746418 | |||||||
| chr17:59746973 | G | A | 25 | a0001c0001t0001g0003 a0001c0001t0001g0076 a0001c0001t0001g0077 others(22): Show |
25 | HG01243.hp1 HG01891.hp2 HG02109.hp2 others(22): Show |
intron_variant | MODIFIER | c.414+8026G>A | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 5/11 | chr17 | 59746973 | |||||||
| chr17:59747284 | T | C | 11 | a0001c0001t0004g0262 a0001c0001t0004g0263 a0001c0001t0004g0265 others(8): Show |
11 | HG01109.hp2 HG02615.hp1 HG02896.hp1 others(8): Show |
intron_variant | MODIFIER | c.414+8337T>C | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 5/11 | chr17 | 59747284 | |||||||
| chr17:59747388 | G | A | 2 | a0001c0001t0002g0027 a0001c0001t0002g0094 |
2 | HG01975.hp1 HG03834.hp2 |
intron_variant | MODIFIER | c.414+8441G>A | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 5/11 | chr17 | 59747388 | |||||||
| chr17:59747410 | TTTC | T | 13 | a0001c0001t0002g0015 a0001c0001t0002g0033 a0001c0001t0002g0035 others(10): Show |
13 | HG00423.hp2 HG02083.hp2 HG02129.hp1 others(10): Show |
intron_variant | MODIFIER | c.414+8466_414+8468d others(5): Show |
VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr17 | 59747410 | ||||||
| chr17:59747413 | C | CT | 86 | a0001c0001t0001g0003 a0001c0001t0001g0076 a0001c0001t0001g0077 others(83): Show |
86 | HG00408.hp2 HG00544.hp1 HG00621.hp1 others(83): Show |
intron_variant | MODIFIER | c.414+8480dupT | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr17 | 59747413 | ||||||
| chr17:59747566 | C | T | 103 | a0001c0001t0001g0003 a0001c0001t0001g0076 a0001c0001t0001g0077 others(100): Show |
103 | HG00408.hp2 HG00423.hp2 HG00544.hp1 others(100): Show |
intron_variant | MODIFIER | c.414+8619C>T | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 5/11 | chr17 | 59747566 | |||||||
| chr17:59747615 | TG | T | 6 | a0001c0001t0003g0149 a0001c0001t0003g0151 a0001c0001t0003g0258 others(3): Show |
6 | HG02896.hp2 HG03195.hp1 HG03209.hp2 others(3): Show |
intron_variant | MODIFIER | c.414+8670delG | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr17 | 59747615 | ||||||
| chr17:59747760 | G | A | 5 | a0001c0001t0003g0154 a0001c0001t0003g0155 a0001c0001t0003g0156 others(2): Show |
5 | HG01168.hp2 HG02486.hp1 HG02615.hp2 others(2): Show |
intron_variant | MODIFIER | c.414+8813G>A | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 5/11 | chr17 | 59747760 | |||||||
| chr17:59747951 | C | G | 1 | a0001c0001t0003g0151 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.414+9004C>G | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 5/11 | chr17 | 59747951 | |||||||
| chr17:59747993 | G | A | 4 | a0001c0001t0006g0283 a0001c0001t0006g0284 a0001c0001t0006g0285 others(1): Show |
4 | HG02109.hp2 HG03130.hp2 HG06807.hp2 others(1): Show |
intron_variant | MODIFIER | c.414+9046G>A | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 5/11 | chr17 | 59747993 | |||||||
| chr17:59748127 | C | G | 11 | a0001c0001t0004g0262 a0001c0001t0004g0263 a0001c0001t0004g0265 others(8): Show |
11 | HG01109.hp2 HG02615.hp1 HG02896.hp1 others(8): Show |
intron_variant | MODIFIER | c.414+9180C>G | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 5/11 | chr17 | 59748127 | |||||||
| chr17:59748195 | CA | C | 228 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(225): Show |
228 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(225): Show |
intron_variant | MODIFIER | c.414+9270delA | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr17 | 59748195 | ||||||
| chr17:59748195 | CAA | C | 9 | a0001c0001t0001g0081 a0001c0001t0001g0084 a0001c0001t0001g0085 others(6): Show |
9 | HG00673.hp2 HG01168.hp2 HG02257.hp1 others(6): Show |
intron_variant | MODIFIER | c.414+9269_414+9270d others(4): Show |
VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr17 | 59748195 | ||||||
| chr17:59748211 | A | C | 79 | a0001c0001t0001g0069 a0001c0001t0001g0070 a0001c0001t0001g0100 others(76): Show |
79 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(76): Show |
intron_variant | MODIFIER | c.414+9264A>C | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 5/11 | chr17 | 59748211 | |||||||
| chr17:59748214 | A | C | 2 | a0001c0001t0004g0268 a0001c0001t0004g0273 |
2 | HG02615.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.414+9267A>C | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 5/11 | chr17 | 59748214 | |||||||
| chr17:59748890 | A | AT | 42 | a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0132 others(39): Show |
42 | HG00438.hp2 HG00738.hp2 HG01069.hp1 others(39): Show |
intron_variant | MODIFIER | c.414+9946dupT | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr17 | 59748890 | ||||||
| chr17:59748890 | A | ATT | 3 | a0001c0001t0003g0116 a0001c0001t0003g0135 a0001c0001t0003g0147 |
3 | NA18949.hp2 NA18967.hp2 NA18992.hp2 |
intron_variant | MODIFIER | c.414+9945_414+9946d others(4): Show |
VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr17 | 59748890 | ||||||
| chr17:59748890 | A | T | 4 | a0001c0001t0001g0086 a0001c0001t0001g0184 a0001c0001t0001g0232 others(1): Show |
4 | HG02280.hp2 HG02615.hp1 HG03831.hp1 others(1): Show |
intron_variant | MODIFIER | c.414+9943A>T | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 5/11 | chr17 | 59748890 | |||||||
| chr17:59748892 | T | TA | 15 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(12): Show |
15 | HG00642.hp1 HG00673.hp2 HG01099.hp1 others(12): Show |
intron_variant | MODIFIER | c.414+9945_414+9946i others(3): Show |
VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 5/11 | chr17 | 59748892 | |||||||
| chr17:59748893 | T | A | 151 | a0001c0001t0001g0003 a0001c0001t0001g0069 a0001c0001t0001g0070 others(148): Show |
151 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(148): Show |
intron_variant | MODIFIER | c.414+9946T>A | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 5/11 | chr17 | 59748893 | |||||||
| chr17:59748893 | TA | T | 3 | a0001c0001t0001g0088 a0001c0001t0001g0092 a0001c0001t0001g0095 |
3 | HG02622.hp2 HG03453.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.414+9947delA | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 5/11 | chr17 | 59748893 | |||||||
| chr17:59748894 | A | T | 278 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(275): Show |
278 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(275): Show |
intron_variant | MODIFIER | c.414+9947A>T | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 5/11 | chr17 | 59748894 | |||||||
| chr17:59748895 | T | A | 1 | a0001c0001t0001g0277 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.414+9948T>A | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 5/11 | chr17 | 59748895 | |||||||
| chr17:59748896 | T | A | 9 | a0001c0001t0001g0077 a0001c0001t0001g0078 a0001c0001t0001g0079 others(6): Show |
9 | HG00639.hp1 HG01243.hp1 HG02027.hp2 others(6): Show |
intron_variant | MODIFIER | c.414+9949T>A | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 5/11 | chr17 | 59748896 | |||||||
| chr17:59749062 | G | C | 5 | a0001c0001t0001g0200 a0001c0001t0001g0231 a0001c0001t0001g0232 others(2): Show |
5 | NA18942.hp2 NA18943.hp2 NA18959.hp1 others(2): Show |
intron_variant | MODIFIER | c.414+10115G>C | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 5/11 | chr17 | 59749062 | |||||||
| chr17:59749115 | A | AT | 8 | a0001c0001t0001g0106 a0001c0001t0001g0187 a0001c0001t0001g0205 others(5): Show |
8 | HG00408.hp1 HG01074.hp2 HG01243.hp2 others(5): Show |
intron_variant | MODIFIER | c.414+10183dupT | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr17 | 59749115 | ||||||
| chr17:59749169 | T | G | 173 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(170): Show |
173 | HG00408.hp2 HG00423.hp2 HG00438.hp2 others(170): Show |
intron_variant | MODIFIER | c.414+10222T>G | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 5/11 | chr17 | 59749169 | |||||||
| chr17:59749244 | A | G | 78 | a0001c0001t0002g0012 a0001c0001t0002g0013 a0001c0001t0002g0014 others(75): Show |
78 | HG00408.hp2 HG00423.hp2 HG00544.hp1 others(75): Show |
intron_variant | MODIFIER | c.414+10297A>G | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 5/11 | chr17 | 59749244 | |||||||
| chr17:59749370 | C | A | 87 | a0001c0001t0001g0069 a0001c0001t0001g0070 a0001c0001t0001g0100 others(84): Show |
87 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(84): Show |
intron_variant | MODIFIER | c.414+10423C>A | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 5/11 | chr17 | 59749370 | |||||||
| chr17:59749430 | A | T | 1 | a0001c0001t0001g0239 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.414+10483A>T | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 5/11 | chr17 | 59749430 | |||||||
| chr17:59749470 | TATAAATC | T | 21 | a0001c0001t0001g0003 a0001c0001t0001g0076 a0001c0001t0001g0077 others(18): Show |
21 | HG01243.hp1 HG01891.hp2 HG02257.hp1 others(18): Show |
intron_variant | MODIFIER | c.414+10525_414+1053 others(11): Show |
VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr17 | 59749470 | ||||||
| chr17:59749610 | A | G | 18 | a0001c0001t0001g0003 a0001c0001t0001g0076 a0001c0001t0001g0077 others(15): Show |
18 | HG01243.hp1 HG01891.hp2 HG02257.hp1 others(15): Show |
intron_variant | MODIFIER | c.414+10663A>G | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 5/11 | chr17 | 59749610 | |||||||
| chr17:59749793 | A | G | 49 | a0001c0001t0001g0132 a0001c0001t0001g0139 a0001c0001t0003g0105 others(46): Show |
49 | HG00438.hp2 HG00642.hp1 HG00673.hp2 others(46): Show |
intron_variant | MODIFIER | c.414+10846A>G | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 5/11 | chr17 | 59749793 | |||||||
| chr17:59749860 | C | T | 11 | a0001c0001t0004g0262 a0001c0001t0004g0263 a0001c0001t0004g0265 others(8): Show |
11 | HG01109.hp2 HG02615.hp1 HG02896.hp1 others(8): Show |
intron_variant | MODIFIER | c.414+10913C>T | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 5/11 | chr17 | 59749860 | |||||||
| chr17:59750057 | G | T | 1 | a0001c0001t0001g0095 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.414+11110G>T | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 5/11 | chr17 | 59750057 | |||||||
| chr17:59750217 | A | G | 1 | a0001c0001t0001g0277 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.414+11270A>G | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 5/11 | chr17 | 59750217 | |||||||
| chr17:59750290 | G | A | 8 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(5): Show |
8 | HG01099.hp1 HG01884.hp1 HG01952.hp2 others(5): Show |
intron_variant | MODIFIER | c.414+11343G>A | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 5/11 | chr17 | 59750290 | |||||||
| chr17:59750302 | A | AT | 171 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(168): Show |
171 | HG00408.hp2 HG00423.hp2 HG00438.hp2 others(168): Show |
intron_variant | MODIFIER | c.414+11371dupT | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr17 | 59750302 | ||||||
| chr17:59750338 | G | A | 1 | a0001c0001t0002g0019 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.414+11391G>A | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 5/11 | chr17 | 59750338 | |||||||
| chr17:59750351 | T | G | 281 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(278): Show |
281 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(278): Show |
intron_variant | MODIFIER | c.414+11404T>G | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 5/11 | chr17 | 59750351 | |||||||
| chr17:59750423 | T | G | 4 | a0001c0001t0001g0207 a0001c0001t0001g0211 a0001c0001t0001g0218 others(1): Show |
4 | HG00280.hp2 HG00639.hp1 HG01255.hp2 others(1): Show |
intron_variant | MODIFIER | c.414+11476T>G | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 5/11 | chr17 | 59750423 | |||||||
| chr17:59750729 | A | G | 1 | a0001c0001t0001g0242 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.414+11782A>G | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 5/11 | chr17 | 59750729 | |||||||
| chr17:59750901 | C | A | 11 | a0001c0001t0004g0262 a0001c0001t0004g0263 a0001c0001t0004g0265 others(8): Show |
11 | HG01109.hp2 HG02615.hp1 HG02896.hp1 others(8): Show |
intron_variant | MODIFIER | c.414+11954C>A | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 5/11 | chr17 | 59750901 | |||||||
| chr17:59750926 | C | CT | 121 | a0001c0001t0001g0003 a0001c0001t0001g0009 a0001c0001t0001g0010 others(118): Show |
121 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(118): Show |
intron_variant | MODIFIER | c.414+12002dupT | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr17 | 59750926 | ||||||
| chr17:59750926 | C | CTT | 18 | a0001c0001t0001g0152 a0001c0001t0001g0278 a0001c0001t0002g0014 others(15): Show |
18 | HG00544.hp1 HG00621.hp1 HG00738.hp1 others(15): Show |
intron_variant | MODIFIER | c.414+12001_414+1200 others(6): Show |
VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr17 | 59750926 | ||||||
| chr17:59750926 | CT | C | 11 | a0001c0001t0003g0127 a0001c0001t0004g0262 a0001c0001t0004g0263 others(8): Show |
11 | HG01069.hp1 HG01109.hp2 HG02896.hp1 others(8): Show |
intron_variant | MODIFIER | c.414+12002delT | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr17 | 59750926 | ||||||
| chr17:59751058 | G | A | 1 | a0001c0001t0003g0131 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.414+12111G>A | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 5/11 | chr17 | 59751058 | |||||||
| chr17:59751355 | A | G | 1 | a0001c0001t0001g0101 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.414+12408A>G | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 5/11 | chr17 | 59751355 | |||||||
| chr17:59751387 | C | T | 1 | a0001c0001t0002g0037 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.414+12440C>T | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 5/11 | chr17 | 59751387 | |||||||
| chr17:59751603 | G | A | 103 | a0001c0001t0001g0003 a0001c0001t0001g0076 a0001c0001t0001g0077 others(100): Show |
103 | HG00408.hp2 HG00423.hp2 HG00544.hp1 others(100): Show |
intron_variant | MODIFIER | c.414+12656G>A | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 5/11 | chr17 | 59751603 | |||||||
| chr17:59751607 | T | G | 1 | a0001c0001t0002g0035 | 1 | NA18993.hp2 | intron_variant | MODIFIER | c.414+12660T>G | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 5/11 | chr17 | 59751607 | |||||||
| chr17:59751607 | T | TG | 92 | a0001c0001t0001g0003 a0001c0001t0001g0076 a0001c0001t0001g0077 others(89): Show |
92 | HG00423.hp2 HG00621.hp1 HG00639.hp2 others(89): Show |
intron_variant | MODIFIER | c.414+12668dupG | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr17 | 59751607 | ||||||
| chr17:59751607 | T | TGG | 17 | a0001c0001t0001g0081 a0001c0001t0001g0095 a0001c0001t0002g0017 others(14): Show |
17 | HG00408.hp2 HG00544.hp1 HG01258.hp1 others(14): Show |
intron_variant | MODIFIER | c.414+12667_414+1266 others(6): Show |
VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr17 | 59751607 | ||||||
| chr17:59751608 | G | T | 11 | a0001c0001t0004g0262 a0001c0001t0004g0263 a0001c0001t0004g0265 others(8): Show |
11 | HG01109.hp2 HG02615.hp1 HG02896.hp1 others(8): Show |
intron_variant | MODIFIER | c.414+12661G>T | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 5/11 | chr17 | 59751608 | |||||||
| chr17:59751643 | C | CTGAGG | 104 | a0001c0001t0001g0003 a0001c0001t0001g0076 a0001c0001t0001g0077 others(101): Show |
104 | HG00408.hp2 HG00423.hp2 HG00544.hp1 others(101): Show |
intron_variant | MODIFIER | c.414+12701_414+1270 others(9): Show |
VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr17 | 59751643 | ||||||
| chr17:59751744 | C | CA | 94 | a0001c0001t0001g0003 a0001c0001t0001g0081 a0001c0001t0001g0089 others(91): Show |
94 | HG00408.hp2 HG00423.hp1 HG00423.hp2 others(91): Show |
intron_variant | MODIFIER | c.414+12821dupA | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr17 | 59751744 | ||||||
| chr17:59751744 | C | CAA | 13 | a0001c0001t0001g0101 a0001c0001t0002g0017 a0001c0001t0002g0034 others(10): Show |
13 | HG00673.hp1 HG01358.hp1 HG01358.hp2 others(10): Show |
intron_variant | MODIFIER | c.414+12820_414+1282 others(6): Show |
VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr17 | 59751744 | ||||||
| chr17:59751744 | CA | C | 6 | a0001c0001t0001g0070 a0001c0001t0001g0163 a0001c0001t0001g0182 others(3): Show |
6 | HG01256.hp1 HG02004.hp2 HG02602.hp1 others(3): Show |
intron_variant | MODIFIER | c.414+12821delA | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr17 | 59751744 | ||||||
| chr17:59751768 | A | G | 1 | a0001c0001t0001g0170 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.414+12821A>G | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 5/11 | chr17 | 59751768 | |||||||
| chr17:59751777 | T | G | 1 | a0001c0001t0001g0252 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.414+12830T>G | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 5/11 | chr17 | 59751777 | |||||||
| chr17:59752041 | C | T | 6 | a0001c0001t0002g0033 a0001c0001t0002g0042 a0001c0001t0002g0043 others(3): Show |
6 | NA18956.hp1 NA18973.hp2 NA18975.hp2 others(3): Show |
intron_variant | MODIFIER | c.415-12930C>T | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 5/11 | chr17 | 59752041 | |||||||
| chr17:59752227 | A | C | 2 | a0001c0001t0007g0274 a0001c0001t0007g0275 |
2 | HG03491.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.415-12744A>C | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 5/11 | chr17 | 59752227 | |||||||
| chr17:59752278 | G | A | 1 | a0001c0001t0001g0095 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.415-12693G>A | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 5/11 | chr17 | 59752278 | |||||||
| chr17:59752631 | G | A | 104 | a0001c0001t0001g0003 a0001c0001t0001g0076 a0001c0001t0001g0077 others(101): Show |
104 | HG00408.hp2 HG00423.hp2 HG00544.hp1 others(101): Show |
intron_variant | MODIFIER | c.415-12340G>A | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 5/11 | chr17 | 59752631 | |||||||
| chr17:59753061 | G | A | 1 | a0001c0001t0001g0254 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.415-11910G>A | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 5/11 | chr17 | 59753061 | |||||||
| chr17:59753065 | G | A | 87 | a0001c0001t0001g0069 a0001c0001t0001g0070 a0001c0001t0001g0100 others(84): Show |
87 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(84): Show |
intron_variant | MODIFIER | c.415-11906G>A | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 5/11 | chr17 | 59753065 | |||||||
| chr17:59753112 | C | A | 87 | a0001c0001t0001g0069 a0001c0001t0001g0070 a0001c0001t0001g0100 others(84): Show |
87 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(84): Show |
intron_variant | MODIFIER | c.415-11859C>A | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 5/11 | chr17 | 59753112 | |||||||
| chr17:59753121 | T | A | 3 | a0001c0001t0002g0041 a0001c0001t0002g0046 a0001c0001t0002g0093 |
3 | HG00621.hp1 NA18962.hp2 NA19007.hp1 |
intron_variant | MODIFIER | c.415-11850T>A | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 5/11 | chr17 | 59753121 | |||||||
| chr17:59753560 | A | G | 11 | a0001c0001t0004g0262 a0001c0001t0004g0263 a0001c0001t0004g0265 others(8): Show |
11 | HG01109.hp2 HG02615.hp1 HG02896.hp1 others(8): Show |
intron_variant | MODIFIER | c.415-11411A>G | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 5/11 | chr17 | 59753560 | |||||||
| chr17:59753671 | T | C | 2 | a0001c0001t0006g0285 a0001c0001t0006g0286 |
2 | HG02109.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.415-11300T>C | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 5/11 | chr17 | 59753671 | |||||||
| chr17:59753672 | A | T | 2 | a0001c0001t0006g0285 a0001c0001t0006g0286 |
2 | HG02109.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.415-11299A>T | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 5/11 | chr17 | 59753672 | |||||||
| chr17:59753827 | A | G | 2 | a0001c0001t0001g0180 a0001c0001t0001g0214 |
2 | NA19057.hp1 NA19077.hp2 |
intron_variant | MODIFIER | c.415-11144A>G | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 5/11 | chr17 | 59753827 | |||||||
| chr17:59754199 | A | T | 1 | a0001c0001t0001g0197 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.415-10772A>T | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 5/11 | chr17 | 59754199 | |||||||
| chr17:59754241 | A | G | 3 | a0001c0001t0001g0280 a0001c0001t0008g0279 a0001c0001t0008g0281 |
3 | HG02145.hp2 HG02818.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.415-10730A>G | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 5/11 | chr17 | 59754241 | |||||||
| chr17:59754428 | T | C | 1 | a0001c0001t0002g0037 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.415-10543T>C | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 5/11 | chr17 | 59754428 | |||||||
| chr17:59754483 | T | A | 3 | a0001c0001t0001g0100 a0001c0001t0001g0101 a0001c0001t0001g0102 |
3 | HG01261.hp2 HG01358.hp2 NA20752.hp1 |
intron_variant | MODIFIER | c.415-10488T>A | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 5/11 | chr17 | 59754483 | |||||||
| chr17:59754829 | A | G | 106 | a0001c0001t0001g0003 a0001c0001t0001g0076 a0001c0001t0001g0077 others(103): Show |
106 | HG00408.hp2 HG00423.hp2 HG00544.hp1 others(103): Show |
intron_variant | MODIFIER | c.415-10142A>G | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 5/11 | chr17 | 59754829 | |||||||
| chr17:59754978 | G | GC | 30 | a0001c0001t0001g0095 a0001c0001t0001g0150 a0001c0001t0001g0153 others(27): Show |
30 | HG00140.hp1 HG01109.hp1 HG01109.hp2 others(27): Show |
intron_variant | MODIFIER | c.415-9985dupC | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr17 | 59754978 | ||||||
| chr17:59754978 | G | GCCC | 27 | a0001c0001t0001g0003 a0001c0001t0001g0077 a0001c0001t0001g0078 others(24): Show |
27 | HG00621.hp1 HG01243.hp1 HG01243.hp2 others(24): Show |
intron_variant | MODIFIER | c.415-9987_415-9985d others(5): Show |
VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr17 | 59754978 | ||||||
| chr17:59754995 | T | G | 1 | a0001c0001t0002g0063 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.415-9976T>G | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 5/11 | chr17 | 59754995 | |||||||
| chr17:59755030 | T | G | 87 | a0001c0001t0001g0069 a0001c0001t0001g0070 a0001c0001t0001g0100 others(84): Show |
87 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(84): Show |
intron_variant | MODIFIER | c.415-9941T>G | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 5/11 | chr17 | 59755030 | |||||||
| chr17:59755095 | CTTCTTTT others(5): Show |
C | 1 | a0001c0001t0001g0205 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.415-9861_415-9850d others(14): Show |
VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr17 | 59755095 | ||||||
| chr17:59755140 | C | G | 49 | a0001c0001t0001g0132 a0001c0001t0001g0139 a0001c0001t0003g0105 others(46): Show |
49 | HG00438.hp2 HG00642.hp1 HG00673.hp2 others(46): Show |
intron_variant | MODIFIER | c.415-9831C>G | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 5/11 | chr17 | 59755140 | |||||||
| chr17:59755523 | G | A | 13 | a0001c0001t0004g0262 a0001c0001t0004g0263 a0001c0001t0004g0265 others(10): Show |
13 | HG01109.hp2 HG02615.hp1 HG02896.hp1 others(10): Show |
intron_variant | MODIFIER | c.415-9448G>A | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 5/11 | chr17 | 59755523 | |||||||
| chr17:59755556 | A | T | 64 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(61): Show |
64 | HG00438.hp2 HG00642.hp1 HG00673.hp2 others(61): Show |
intron_variant | MODIFIER | c.415-9415A>T | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 5/11 | chr17 | 59755556 | |||||||
| chr17:59755742 | G | GT | 18 | a0001c0001t0001g0103 a0001c0001t0001g0150 a0001c0001t0001g0190 others(15): Show |
18 | HG00621.hp1 HG01109.hp2 HG02615.hp1 others(15): Show |
intron_variant | MODIFIER | c.415-9215dupT | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr17 | 59755742 | ||||||
| chr17:59755742 | G | GTT | 10 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(7): Show |
10 | HG01099.hp1 HG01168.hp2 HG01884.hp1 others(7): Show |
intron_variant | MODIFIER | c.415-9216_415-9215d others(4): Show |
VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr17 | 59755742 | ||||||
| chr17:59755742 | G | GTTT | 43 | a0001c0001t0001g0132 a0001c0001t0001g0139 a0001c0001t0003g0105 others(40): Show |
43 | HG00438.hp2 HG00642.hp1 HG00673.hp2 others(40): Show |
intron_variant | MODIFIER | c.415-9217_415-9215d others(5): Show |
VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr17 | 59755742 | ||||||
| chr17:59755742 | G | GTTTT | 11 | a0001c0001t0003g0117 a0001c0001t0003g0120 a0001c0001t0003g0133 others(8): Show |
11 | HG02027.hp2 HG02071.hp2 HG02486.hp1 others(8): Show |
intron_variant | MODIFIER | c.415-9218_415-9215d others(6): Show |
VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr17 | 59755742 | ||||||
| chr17:59755745 | T | G | 4 | a0001c0001t0001g0175 a0001c0001t0001g0220 a0001c0001t0001g0225 others(1): Show |
4 | HG00642.hp2 HG01978.hp2 HG01981.hp1 others(1): Show |
intron_variant | MODIFIER | c.415-9226T>G | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 5/11 | chr17 | 59755745 | |||||||
| chr17:59755986 | C | T | 1 | a0001c0001t0001g0086 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.415-8985C>T | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 5/11 | chr17 | 59755986 | |||||||
| chr17:59756115 | T | C | 64 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(61): Show |
64 | HG00438.hp2 HG00642.hp1 HG00673.hp2 others(61): Show |
intron_variant | MODIFIER | c.415-8856T>C | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 5/11 | chr17 | 59756115 | |||||||
| chr17:59756181 | C | T | 1 | a0001c0001t0001g0242 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.415-8790C>T | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 5/11 | chr17 | 59756181 | |||||||
| chr17:59756270 | T | C | 1 | a0001c0001t0002g0039 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.415-8701T>C | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 5/11 | chr17 | 59756270 | |||||||
| chr17:59756334 | A | G | 5 | a0001c0001t0004g0262 a0001c0001t0004g0263 a0001c0001t0004g0267 others(2): Show |
5 | HG01109.hp2 HG02896.hp1 HG03486.hp2 others(2): Show |
intron_variant | MODIFIER | c.415-8637A>G | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 5/11 | chr17 | 59756334 | |||||||
| chr17:59756585 | A | G | 266 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(263): Show |
266 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(263): Show |
intron_variant | MODIFIER | c.415-8386A>G | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 5/11 | chr17 | 59756585 | |||||||
| chr17:59756685 | C | T | 1 | a0001c0001t0001g0090 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.415-8286C>T | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 5/11 | chr17 | 59756685 | |||||||
| chr17:59757157 | G | C | 11 | a0001c0001t0004g0262 a0001c0001t0004g0263 a0001c0001t0004g0265 others(8): Show |
11 | HG01109.hp2 HG02615.hp1 HG02896.hp1 others(8): Show |
intron_variant | MODIFIER | c.415-7814G>C | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 5/11 | chr17 | 59757157 | |||||||
| chr17:59757238 | G | GAGAT | 24 | a0001c0001t0001g0083 a0001c0001t0001g0088 a0001c0001t0001g0091 others(21): Show |
24 | HG00544.hp2 HG00741.hp1 HG01109.hp1 others(21): Show |
intron_variant | MODIFIER | c.415-7680_415-7677d others(6): Show |
VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr17 | 59757238 | ||||||
| chr17:59757238 | G | GAGATAGA others(1): Show |
6 | a0001c0001t0001g0187 a0001c0001t0002g0054 a0001c0001t0002g0097 others(3): Show |
6 | HG01069.hp2 HG01071.hp2 HG01358.hp1 others(3): Show |
intron_variant | MODIFIER | c.415-7684_415-7677d others(10): Show |
VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr17 | 59757238 | ||||||
| chr17:59757238 | GAGAT | G | 108 | a0001c0001t0001g0008 a0001c0001t0001g0070 a0001c0001t0001g0076 others(105): Show |
108 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(105): Show |
intron_variant | MODIFIER | c.415-7680_415-7677d others(6): Show |
VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr17 | 59757238 | ||||||
| chr17:59757238 | GAGATAGA others(1): Show |
G | 62 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(59): Show |
62 | HG00642.hp1 HG00673.hp2 HG00738.hp2 others(59): Show |
intron_variant | MODIFIER | c.415-7684_415-7677d others(10): Show |
VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr17 | 59757238 | ||||||
| chr17:59757238 | GAGATAGA others(5): Show |
G | 5 | a0001c0001t0001g0211 a0001c0001t0003g0131 a0001c0001t0003g0155 others(2): Show |
5 | HG00639.hp1 HG02615.hp1 HG02615.hp2 others(2): Show |
intron_variant | MODIFIER | c.415-7688_415-7677d others(14): Show |
VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr17 | 59757238 | ||||||
| chr17:59757238 | GAGATAGA others(9): Show |
G | 9 | a0001c0001t0004g0262 a0001c0001t0004g0263 a0001c0001t0004g0265 others(6): Show |
9 | HG01109.hp2 HG02896.hp1 HG02965.hp2 others(6): Show |
intron_variant | MODIFIER | c.415-7692_415-7677d others(18): Show |
VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr17 | 59757238 | ||||||
| chr17:59757241 | A | C | 1 | a0001c0001t0003g0147 | 1 | NA18992.hp2 | intron_variant | MODIFIER | c.415-7730A>C | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 5/11 | chr17 | 59757241 | |||||||
| chr17:59757245 | A | C | 11 | a0001c0001t0003g0108 a0001c0001t0003g0121 a0001c0001t0003g0122 others(8): Show |
11 | HG00438.hp2 HG01069.hp1 HG02015.hp1 others(8): Show |
intron_variant | MODIFIER | c.415-7726A>C | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 5/11 | chr17 | 59757245 | |||||||
| chr17:59757249 | A | C | 41 | a0001c0001t0001g0132 a0001c0001t0001g0139 a0001c0001t0001g0277 others(38): Show |
41 | HG00642.hp1 HG00673.hp2 HG00738.hp2 others(38): Show |
intron_variant | MODIFIER | c.415-7722A>C | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 5/11 | chr17 | 59757249 | |||||||
| chr17:59757253 | A | C | 2 | a0001c0001t0003g0131 a0001c0001t0003g0155 |
2 | HG02615.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.415-7718A>C | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 5/11 | chr17 | 59757253 | |||||||
| chr17:59757277 | A | G | 1 | a0001c0001t0001g0210 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.415-7694A>G | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 5/11 | chr17 | 59757277 | |||||||
| chr17:59757610 | T | A | 1 | a0001c0001t0002g0054 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.415-7361T>A | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 5/11 | chr17 | 59757610 | |||||||
| chr17:59757803 | T | C | 1 | a0001c0001t0002g0049 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.415-7168T>C | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 5/11 | chr17 | 59757803 | |||||||
| chr17:59757855 | G | GC | 86 | a0001c0001t0001g0003 a0001c0001t0001g0076 a0001c0001t0001g0077 others(83): Show |
86 | HG00408.hp2 HG00423.hp2 HG00544.hp1 others(83): Show |
intron_variant | MODIFIER | c.415-7114dupC | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr17 | 59757855 | ||||||
| chr17:59757858 | A | C | 167 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(164): Show |
167 | HG00408.hp2 HG00423.hp2 HG00438.hp2 others(164): Show |
intron_variant | MODIFIER | c.415-7113A>C | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 5/11 | chr17 | 59757858 | |||||||
| chr17:59757859 | C | CCT | 9 | a0001c0001t0001g0090 a0001c0001t0001g0276 a0001c0001t0002g0014 others(6): Show |
9 | HG00741.hp1 HG02027.hp1 HG02135.hp1 others(6): Show |
intron_variant | MODIFIER | c.415-7112_415-7111i others(4): Show |
VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 5/11 | chr17 | 59757859 | |||||||
| chr17:59757859 | C | CTTT | 31 | a0001c0001t0001g0106 a0001c0001t0001g0177 a0001c0001t0001g0178 others(28): Show |
31 | HG00408.hp1 HG00438.hp1 HG00673.hp2 others(28): Show |
intron_variant | MODIFIER | c.415-7089_415-7087d others(5): Show |
VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr17 | 59757859 | ||||||
| chr17:59757859 | C | CTTTT | 85 | a0001c0001t0001g0069 a0001c0001t0001g0070 a0001c0001t0001g0100 others(82): Show |
85 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(82): Show |
intron_variant | MODIFIER | c.415-7090_415-7087d others(6): Show |
VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr17 | 59757859 | ||||||
| chr17:59757859 | C | CTTTTT | 21 | a0001c0001t0001g0095 a0001c0001t0001g0101 a0001c0001t0001g0103 others(18): Show |
21 | HG00423.hp1 HG00438.hp2 HG00642.hp2 others(18): Show |
intron_variant | MODIFIER | c.415-7091_415-7087d others(7): Show |
VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr17 | 59757859 | ||||||
| chr17:59757859 | CTT | C | 11 | a0001c0001t0004g0262 a0001c0001t0004g0263 a0001c0001t0004g0265 others(8): Show |
11 | HG01109.hp2 HG02615.hp1 HG02896.hp1 others(8): Show |
intron_variant | MODIFIER | c.415-7088_415-7087d others(4): Show |
VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr17 | 59757859 | ||||||
| chr17:59757859 | CTTTTTTT others(6): Show |
C | 1 | a0001c0001t0003g0133 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.415-7099_415-7087d others(15): Show |
VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr17 | 59757859 | ||||||
| chr17:59757860 | T | C | 10 | a0001c0001t0001g0079 a0001c0001t0001g0089 a0001c0001t0002g0027 others(7): Show |
10 | HG02015.hp2 HG02451.hp2 HG02486.hp2 others(7): Show |
intron_variant | MODIFIER | c.415-7111T>C | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 5/11 | chr17 | 59757860 | |||||||
| chr17:59757861 | T | C | 1 | a0001c0001t0005g0061 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.415-7110T>C | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 5/11 | chr17 | 59757861 | |||||||
| chr17:59758035 | C | G | 2 | a0001c0001t0001g0088 a0001c0001t0001g0090 |
2 | HG02622.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.415-6936C>G | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 5/11 | chr17 | 59758035 | |||||||
| chr17:59758073 | C | G | 1 | a0001c0001t0001g0152 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.415-6898C>G | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 5/11 | chr17 | 59758073 | |||||||
| chr17:59758189 | A | G | 2 | a0001c0001t0001g0174 a0001c0001t0001g0212 |
2 | NA18977.hp1 NA18989.hp1 |
intron_variant | MODIFIER | c.415-6782A>G | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 5/11 | chr17 | 59758189 | |||||||
| chr17:59758390 | G | A | 1 | a0001c0001t0001g0076 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.415-6581G>A | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 5/11 | chr17 | 59758390 | |||||||
| chr17:59758429 | C | A | 17 | a0001c0001t0003g0110 a0001c0001t0003g0115 a0001c0001t0003g0116 others(14): Show |
17 | HG00673.hp2 HG00738.hp2 HG01069.hp1 others(14): Show |
intron_variant | MODIFIER | c.415-6542C>A | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 5/11 | chr17 | 59758429 | |||||||
| chr17:59758773 | C | T | 260 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(257): Show |
260 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(257): Show |
intron_variant | MODIFIER | c.415-6198C>T | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 5/11 | chr17 | 59758773 | |||||||
| chr17:59758946 | C | T | 1 | a0001c0001t0001g0095 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.415-6025C>T | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 5/11 | chr17 | 59758946 | |||||||
| chr17:59759010 | C | T | 1 | a0001c0001t0001g0201 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.415-5961C>T | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 5/11 | chr17 | 59759010 | |||||||
| chr17:59759192 | G | A | 58 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(55): Show |
58 | HG00438.hp2 HG00642.hp1 HG00673.hp2 others(55): Show |
intron_variant | MODIFIER | c.415-5779G>A | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 5/11 | chr17 | 59759192 | |||||||
| chr17:59759242 | C | T | 1 | a0001c0001t0004g0262 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.415-5729C>T | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 5/11 | chr17 | 59759242 | |||||||
| chr17:59759243 | G | A | 1 | a0001c0001t0003g0157 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.415-5728G>A | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 5/11 | chr17 | 59759243 | |||||||
| chr17:59759296 | C | T | 1 | a0001c0001t0001g0070 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.415-5675C>T | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 5/11 | chr17 | 59759296 | |||||||
| chr17:59759377 | AAAAAT | A | 87 | a0001c0001t0001g0069 a0001c0001t0001g0070 a0001c0001t0001g0100 others(84): Show |
87 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(84): Show |
intron_variant | MODIFIER | c.415-5585_415-5581d others(7): Show |
VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr17 | 59759377 | ||||||
| chr17:59759406 | A | G | 78 | a0001c0001t0002g0012 a0001c0001t0002g0013 a0001c0001t0002g0014 others(75): Show |
78 | HG00408.hp2 HG00423.hp2 HG00544.hp1 others(75): Show |
intron_variant | MODIFIER | c.415-5565A>G | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 5/11 | chr17 | 59759406 | |||||||
| chr17:59759563 | A | G | 179 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(176): Show |
179 | HG00408.hp2 HG00423.hp2 HG00438.hp2 others(176): Show |
intron_variant | MODIFIER | c.415-5408A>G | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 5/11 | chr17 | 59759563 | |||||||
| chr17:59759745 | G | C | 2 | a0001c0001t0004g0269 a0001c0001t0004g0270 |
2 | HG03041.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.415-5226G>C | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 5/11 | chr17 | 59759745 | |||||||
| chr17:59759842 | C | T | 11 | a0001c0001t0004g0262 a0001c0001t0004g0263 a0001c0001t0004g0265 others(8): Show |
11 | HG01109.hp2 HG02615.hp1 HG02896.hp1 others(8): Show |
intron_variant | MODIFIER | c.415-5129C>T | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 5/11 | chr17 | 59759842 | |||||||
| chr17:59759903 | GT | G | 103 | a0001c0001t0001g0076 a0001c0001t0001g0081 a0001c0001t0001g0082 others(100): Show |
103 | HG00408.hp2 HG00423.hp2 HG00544.hp1 others(100): Show |
intron_variant | MODIFIER | c.415-5048delT | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr17 | 59759903 | ||||||
| chr17:59759903 | GTT | G | 16 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(13): Show |
16 | HG00741.hp1 HG01099.hp1 HG01243.hp1 others(13): Show |
intron_variant | MODIFIER | c.415-5049_415-5048d others(4): Show |
VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr17 | 59759903 | ||||||
| chr17:59759908 | T | TG | 85 | a0001c0001t0001g0069 a0001c0001t0001g0070 a0001c0001t0001g0100 others(82): Show |
85 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(82): Show |
intron_variant | MODIFIER | c.415-5063_415-5062i others(3): Show |
VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 5/11 | chr17 | 59759908 | |||||||
| chr17:59759909 | T | G | 58 | a0001c0001t0001g0089 a0001c0001t0001g0132 a0001c0001t0001g0139 others(55): Show |
58 | HG00438.hp2 HG00621.hp1 HG00642.hp1 others(55): Show |
intron_variant | MODIFIER | c.415-5062T>G | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 5/11 | chr17 | 59759909 | |||||||
| chr17:59759910 | T | G | 104 | a0001c0001t0001g0076 a0001c0001t0001g0081 a0001c0001t0001g0082 others(101): Show |
104 | HG00408.hp2 HG00423.hp2 HG00544.hp1 others(101): Show |
intron_variant | MODIFIER | c.415-5061T>G | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 5/11 | chr17 | 59759910 | |||||||
| chr17:59759911 | T | G | 18 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(15): Show |
18 | HG00741.hp1 HG01099.hp1 HG01243.hp1 others(15): Show |
intron_variant | MODIFIER | c.415-5060T>G | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 5/11 | chr17 | 59759911 | |||||||
| chr17:59759912 | T | G | 8 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(5): Show |
8 | HG01099.hp1 HG01884.hp1 HG01952.hp2 others(5): Show |
intron_variant | MODIFIER | c.415-5059T>G | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 5/11 | chr17 | 59759912 | |||||||
| chr17:59760122 | CA | C | 178 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(175): Show |
178 | HG00408.hp2 HG00423.hp2 HG00438.hp2 others(175): Show |
intron_variant | MODIFIER | c.415-4837delA | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr17 | 59760122 | ||||||
| chr17:59760136 | A | G | 1 | a0001c0001t0001g0095 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.415-4835A>G | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 5/11 | chr17 | 59760136 | |||||||
| chr17:59760262 | C | T | 1 | a0001c0001t0001g0188 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.415-4709C>T | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 5/11 | chr17 | 59760262 | |||||||
| chr17:59760500 | A | G | 1 | a0001c0001t0003g0115 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.415-4471A>G | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 5/11 | chr17 | 59760500 | |||||||
| chr17:59760520 | C | T | 2 | a0001c0001t0001g0213 a0001c0001t0001g0282 |
2 | HG01099.hp2 HG02683.hp1 |
intron_variant | MODIFIER | c.415-4451C>T | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 5/11 | chr17 | 59760520 | |||||||
| chr17:59760524 | T | C | 8 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(5): Show |
8 | HG01099.hp1 HG01884.hp1 HG01952.hp2 others(5): Show |
intron_variant | MODIFIER | c.415-4447T>C | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 5/11 | chr17 | 59760524 | |||||||
| chr17:59760679 | G | A | 56 | a0001c0001t0001g0132 a0001c0001t0001g0139 a0001c0001t0001g0277 others(53): Show |
56 | HG00438.hp2 HG00642.hp1 HG00673.hp2 others(53): Show |
intron_variant | MODIFIER | c.415-4292G>A | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 5/11 | chr17 | 59760679 | |||||||
| chr17:59760714 | G | A | 1 | a0001c0001t0001g0201 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.415-4257G>A | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 5/11 | chr17 | 59760714 | |||||||
| chr17:59760920 | A | G | 1 | a0001c0001t0002g0065 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.415-4051A>G | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 5/11 | chr17 | 59760920 | |||||||
| chr17:59761006 | G | A | 8 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(5): Show |
8 | HG01099.hp1 HG01884.hp1 HG01952.hp2 others(5): Show |
intron_variant | MODIFIER | c.415-3965G>A | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 5/11 | chr17 | 59761006 | |||||||
| chr17:59761063 | C | T | 1 | a0001c0001t0001g0095 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.415-3908C>T | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 5/11 | chr17 | 59761063 | |||||||
| chr17:59761064 | G | A | 1 | a0001c0001t0001g0088 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.415-3907G>A | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 5/11 | chr17 | 59761064 | |||||||
| chr17:59761342 | G | A | 1 | a0001c0001t0002g0013 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.415-3629G>A | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 5/11 | chr17 | 59761342 | |||||||
| chr17:59761362 | T | C | 1 | a0001c0001t0001g0277 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.415-3609T>C | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 5/11 | chr17 | 59761362 | |||||||
| chr17:59761470 | G | A | 56 | a0001c0001t0001g0132 a0001c0001t0001g0139 a0001c0001t0001g0277 others(53): Show |
56 | HG00438.hp2 HG00642.hp1 HG00673.hp2 others(53): Show |
intron_variant | MODIFIER | c.415-3501G>A | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 5/11 | chr17 | 59761470 | |||||||
| chr17:59761823 | T | C | 1 | a0001c0001t0002g0031 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.415-3148T>C | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 5/11 | chr17 | 59761823 | |||||||
| chr17:59761823 | T | TTC | 265 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(262): Show |
265 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(262): Show |
intron_variant | MODIFIER | c.415-3144_415-3143d others(4): Show |
VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr17 | 59761823 | ||||||
| chr17:59761901 | G | A | 1 | a0001c0001t0001g0277 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.415-3070G>A | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 5/11 | chr17 | 59761901 | |||||||
| chr17:59761926 | C | T | 1 | a0001c0001t0002g0072 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.415-3045C>T | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 5/11 | chr17 | 59761926 | |||||||
| chr17:59761948 | T | C | 1 | a0001c0001t0001g0201 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.415-3023T>C | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 5/11 | chr17 | 59761948 | |||||||
| chr17:59762178 | G | A | 3 | a0001c0001t0002g0193 a0001c0001t0002g0196 a0001c0001t0002g0234 |
3 | HG01069.hp2 HG01071.hp2 HG01358.hp1 |
intron_variant | MODIFIER | c.415-2793G>A | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 5/11 | chr17 | 59762178 | |||||||
| chr17:59762207 | A | G | 179 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(176): Show |
179 | HG00408.hp2 HG00423.hp2 HG00438.hp2 others(176): Show |
intron_variant | MODIFIER | c.415-2764A>G | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 5/11 | chr17 | 59762207 | |||||||
| chr17:59762243 | C | T | 78 | a0001c0001t0002g0012 a0001c0001t0002g0013 a0001c0001t0002g0014 others(75): Show |
78 | HG00408.hp2 HG00423.hp2 HG00544.hp1 others(75): Show |
intron_variant | MODIFIER | c.415-2728C>T | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 5/11 | chr17 | 59762243 | |||||||
| chr17:59762549 | G | A | 11 | a0001c0001t0004g0262 a0001c0001t0004g0263 a0001c0001t0004g0265 others(8): Show |
11 | HG01109.hp2 HG02615.hp1 HG02896.hp1 others(8): Show |
intron_variant | MODIFIER | c.415-2422G>A | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 5/11 | chr17 | 59762549 | |||||||
| chr17:59762762 | A | G | 1 | a0001c0001t0001g0095 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.415-2209A>G | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 5/11 | chr17 | 59762762 | |||||||
| chr17:59762856 | AT | A | 11 | a0001c0001t0004g0262 a0001c0001t0004g0263 a0001c0001t0004g0265 others(8): Show |
11 | HG01109.hp2 HG02615.hp1 HG02896.hp1 others(8): Show |
intron_variant | MODIFIER | c.415-2113delT | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr17 | 59762856 | ||||||
| chr17:59762903 | G | T | 1 | a0001c0001t0002g0056 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.415-2068G>T | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 5/11 | chr17 | 59762903 | |||||||
| chr17:59763172 | C | T | 2 | a0001c0001t0004g0265 a0001c0001t0004g0266 |
2 | HG02970.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.415-1799C>T | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 5/11 | chr17 | 59763172 | |||||||
| chr17:59763480 | G | A | 55 | a0001c0001t0001g0132 a0001c0001t0001g0139 a0001c0001t0003g0105 others(52): Show |
55 | HG00438.hp2 HG00642.hp1 HG00673.hp2 others(52): Show |
intron_variant | MODIFIER | c.415-1491G>A | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 5/11 | chr17 | 59763480 | |||||||
| chr17:59763546 | A | G | 4 | a0001c0001t0001g0176 a0001c0001t0001g0188 a0001c0001t0001g0230 others(1): Show |
4 | HG01074.hp2 HG01361.hp2 HG02280.hp1 others(1): Show |
intron_variant | MODIFIER | c.415-1425A>G | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 5/11 | chr17 | 59763546 | |||||||
| chr17:59763961 | A | G | 11 | a0001c0001t0004g0262 a0001c0001t0004g0263 a0001c0001t0004g0265 others(8): Show |
11 | HG01109.hp2 HG02615.hp1 HG02896.hp1 others(8): Show |
intron_variant | MODIFIER | c.415-1010A>G | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 5/11 | chr17 | 59763961 | |||||||
| chr17:59763996 | A | G | 78 | a0001c0001t0002g0012 a0001c0001t0002g0013 a0001c0001t0002g0014 others(75): Show |
78 | HG00408.hp2 HG00423.hp2 HG00544.hp1 others(75): Show |
intron_variant | MODIFIER | c.415-975A>G | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 5/11 | chr17 | 59763996 | |||||||
| chr17:59764484 | T | C | 1 | a0001c0001t0003g0134 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.415-487T>C | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 5/11 | chr17 | 59764484 | |||||||
| chr17:59764694 | C | T | 8 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(5): Show |
8 | HG01099.hp1 HG01884.hp1 HG01952.hp2 others(5): Show |
intron_variant | MODIFIER | c.415-277C>T | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 5/11 | chr17 | 59764694 | |||||||
| chr17:59764766 | A | G | 2 | a0001c0001t0003g0111 a0001c0001t0003g0112 |
2 | HG01071.hp1 HG03834.hp1 |
intron_variant | MODIFIER | c.415-205A>G | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 5/11 | chr17 | 59764766 | |||||||
| chr17:59764906 | A | T | 1 | a0001c0001t0002g0036 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.415-65A>T | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 5/11 | chr17 | 59764906 | |||||||
| chr17:59765375 | G | T | 64 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(61): Show |
64 | HG00438.hp2 HG00642.hp1 HG00673.hp2 others(61): Show |
intron_variant | MODIFIER | c.582+237G>T | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 6/11 | chr17 | 59765375 | |||||||
| chr17:59765398 | T | C | 11 | a0001c0001t0004g0262 a0001c0001t0004g0263 a0001c0001t0004g0265 others(8): Show |
11 | HG01109.hp2 HG02615.hp1 HG02896.hp1 others(8): Show |
intron_variant | MODIFIER | c.582+260T>C | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 6/11 | chr17 | 59765398 | |||||||
| chr17:59765404 | C | T | 269 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(266): Show |
269 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(266): Show |
intron_variant | MODIFIER | c.582+266C>T | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 6/11 | chr17 | 59765404 | |||||||
| chr17:59765648 | A | G | 4 | a0001c0001t0006g0283 a0001c0001t0006g0284 a0001c0001t0006g0285 others(1): Show |
4 | HG02109.hp2 HG03130.hp2 HG06807.hp2 others(1): Show |
intron_variant | MODIFIER | c.582+510A>G | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 6/11 | chr17 | 59765648 | |||||||
| chr17:59765947 | T | TA | 6 | a0001c0001t0003g0154 a0001c0001t0003g0155 a0001c0001t0003g0156 others(3): Show |
6 | HG01168.hp2 HG02027.hp2 HG02486.hp1 others(3): Show |
intron_variant | MODIFIER | c.582+810dupA | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr17 | 59765947 | ||||||
| chr17:59766291 | G | A | 1 | a0001c0001t0001g0095 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.582+1153G>A | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 6/11 | chr17 | 59766291 | |||||||
| chr17:59766340 | C | A | 1 | a0001c0001t0001g0282 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.582+1202C>A | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 6/11 | chr17 | 59766340 | |||||||
| chr17:59766452 | C | T | 1 | a0001c0001t0002g0062 | 1 | NA18949.hp1 | intron_variant | MODIFIER | c.582+1314C>T | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 6/11 | chr17 | 59766452 | |||||||
| chr17:59766465 | C | T | 2 | a0001c0001t0006g0283 a0001c0001t0006g0284 |
2 | HG03130.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.582+1327C>T | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 6/11 | chr17 | 59766465 | |||||||
| chr17:59766843 | A | G | 266 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(263): Show |
266 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(263): Show |
intron_variant | MODIFIER | c.582+1705A>G | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 6/11 | chr17 | 59766843 | |||||||
| chr17:59766970 | C | T | 1 | a0001c0001t0002g0064 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.582+1832C>T | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 6/11 | chr17 | 59766970 | |||||||
| chr17:59767025 | A | C | 1 | a0001c0001t0001g0092 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.582+1887A>C | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 6/11 | chr17 | 59767025 | |||||||
| chr17:59767123 | G | T | 1 | a0001c0001t0001g0095 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.582+1985G>T | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 6/11 | chr17 | 59767123 | |||||||
| chr17:59767337 | T | C | 1 | a0001c0001t0001g0090 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.582+2199T>C | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 6/11 | chr17 | 59767337 | |||||||
| chr17:59767698 | G | A | 1 | a0001c0001t0010g0228 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.582+2560G>A | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 6/11 | chr17 | 59767698 | |||||||
| chr17:59767919 | G | A | 1 | a0001c0001t0001g0095 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.582+2781G>A | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 6/11 | chr17 | 59767919 | |||||||
| chr17:59767960 | A | G | 103 | a0001c0001t0001g0003 a0001c0001t0001g0076 a0001c0001t0001g0077 others(100): Show |
103 | HG00408.hp2 HG00423.hp2 HG00544.hp1 others(100): Show |
intron_variant | MODIFIER | c.582+2822A>G | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 6/11 | chr17 | 59767960 | |||||||
| chr17:59768109 | CA | C | 179 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(176): Show |
179 | HG00408.hp2 HG00423.hp2 HG00438.hp2 others(176): Show |
intron_variant | MODIFIER | c.582+2981delA | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr17 | 59768109 | ||||||
| chr17:59768225 | G | A | 1 | a0001c0001t0002g0034 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.582+3087G>A | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 6/11 | chr17 | 59768225 | |||||||
| chr17:59768263 | A | C | 87 | a0001c0001t0001g0069 a0001c0001t0001g0070 a0001c0001t0001g0100 others(84): Show |
87 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(84): Show |
intron_variant | MODIFIER | c.582+3125A>C | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 6/11 | chr17 | 59768263 | |||||||
| chr17:59768576 | C | T | 1 | a0001c0001t0001g0277 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.582+3438C>T | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 6/11 | chr17 | 59768576 | |||||||
| chr17:59768649 | T | C | 1 | a0001c0001t0001g0095 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.582+3511T>C | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 6/11 | chr17 | 59768649 | |||||||
| chr17:59768706 | G | C | 2 | a0001c0001t0001g0179 a0001c0001t0001g0202 |
2 | HG00423.hp1 HG03654.hp2 |
intron_variant | MODIFIER | c.582+3568G>C | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 6/11 | chr17 | 59768706 | |||||||
| chr17:59768908 | G | A | 49 | a0001c0001t0001g0132 a0001c0001t0001g0139 a0001c0001t0003g0105 others(46): Show |
49 | HG00438.hp2 HG00642.hp1 HG00673.hp2 others(46): Show |
intron_variant | MODIFIER | c.582+3770G>A | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 6/11 | chr17 | 59768908 | |||||||
| chr17:59768940 | G | T | 1 | a0001c0001t0001g0256 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.582+3802G>T | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 6/11 | chr17 | 59768940 | |||||||
| chr17:59769018 | C | T | 1 | a0001c0001t0009g0109 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.582+3880C>T | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 6/11 | chr17 | 59769018 | |||||||
| chr17:59769154 | CT | C | 258 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(255): Show |
258 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(255): Show |
intron_variant | MODIFIER | c.582+4033delT | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr17 | 59769154 | ||||||
| chr17:59769154 | CTT | C | 6 | a0001c0001t0001g0139 a0001c0001t0001g0248 a0001c0001t0001g0254 others(3): Show |
6 | HG01256.hp2 HG02698.hp1 HG03130.hp1 others(3): Show |
intron_variant | MODIFIER | c.582+4032_582+4033d others(4): Show |
VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr17 | 59769154 | ||||||
| chr17:59769525 | GTCTTTGA others(5): Show |
G | 1 | a0001c0001t0002g0050 | 1 | NA18987.hp2 | intron_variant | MODIFIER | c.583-4219_583-4208d others(14): Show |
VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr17 | 59769525 | ||||||
| chr17:59769714 | C | T | 2 | a0001c0001t0007g0274 a0001c0001t0007g0275 |
2 | HG03491.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.583-4040C>T | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 6/11 | chr17 | 59769714 | |||||||
| chr17:59769923 | T | G | 1 | a0001c0001t0001g0256 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.583-3831T>G | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 6/11 | chr17 | 59769923 | |||||||
| chr17:59770262 | T | C | 1 | a0001c0001t0002g0041 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.583-3492T>C | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 6/11 | chr17 | 59770262 | |||||||
| chr17:59770645 | A | G | 179 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(176): Show |
179 | HG00408.hp2 HG00423.hp2 HG00438.hp2 others(176): Show |
intron_variant | MODIFIER | c.583-3109A>G | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 6/11 | chr17 | 59770645 | |||||||
| chr17:59770673 | C | T | 1 | a0001c0001t0001g0095 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.583-3081C>T | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 6/11 | chr17 | 59770673 | |||||||
| chr17:59770823 | T | G | 179 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(176): Show |
179 | HG00408.hp2 HG00423.hp2 HG00438.hp2 others(176): Show |
intron_variant | MODIFIER | c.583-2931T>G | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 6/11 | chr17 | 59770823 | |||||||
| chr17:59770990 | G | GT | 12 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(9): Show |
12 | HG01099.hp1 HG01884.hp1 HG01952.hp2 others(9): Show |
intron_variant | MODIFIER | c.583-2752dupT | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr17 | 59770990 | ||||||
| chr17:59771044 | C | T | 1 | a0001c0001t0002g0050 | 1 | NA18987.hp2 | intron_variant | MODIFIER | c.583-2710C>T | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 6/11 | chr17 | 59771044 | |||||||
| chr17:59771166 | C | CT | 180 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(177): Show |
180 | HG00408.hp2 HG00423.hp2 HG00438.hp2 others(177): Show |
intron_variant | MODIFIER | c.583-2576dupT | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr17 | 59771166 | ||||||
| chr17:59771226 | G | A | 1 | a0001c0001t0001g0175 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.583-2528G>A | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 6/11 | chr17 | 59771226 | |||||||
| chr17:59771237 | A | G | 6 | a0001c0001t0002g0192 a0001c0001t0002g0193 a0001c0001t0002g0194 others(3): Show |
6 | HG00741.hp1 HG01069.hp2 HG01071.hp2 others(3): Show |
intron_variant | MODIFIER | c.583-2517A>G | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 6/11 | chr17 | 59771237 | |||||||
| chr17:59771378 | C | T | 2 | a0001c0001t0003g0105 a0001c0001t0003g0148 |
2 | HG02257.hp2 HG02647.hp1 |
intron_variant | MODIFIER | c.583-2376C>T | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 6/11 | chr17 | 59771378 | |||||||
| chr17:59771379 | G | A | 1 | a0001c0001t0001g0203 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.583-2375G>A | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 6/11 | chr17 | 59771379 | |||||||
| chr17:59771606 | G | GT | 47 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(44): Show |
47 | HG00544.hp2 HG00621.hp1 HG00621.hp2 others(44): Show |
intron_variant | MODIFIER | c.583-2129dupT | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr17 | 59771606 | ||||||
| chr17:59771606 | GT | G | 7 | a0001c0001t0001g0095 a0001c0001t0001g0165 a0001c0001t0001g0171 others(4): Show |
7 | HG01891.hp1 HG02559.hp2 HG03471.hp1 others(4): Show |
intron_variant | MODIFIER | c.583-2129delT | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr17 | 59771606 | ||||||
| chr17:59771899 | A | C | 1 | a0001c0001t0006g0285 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.583-1855A>C | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 6/11 | chr17 | 59771899 | |||||||
| chr17:59772095 | G | A | 179 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(176): Show |
179 | HG00408.hp2 HG00423.hp2 HG00438.hp2 others(176): Show |
intron_variant | MODIFIER | c.583-1659G>A | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 6/11 | chr17 | 59772095 | |||||||
| chr17:59772325 | T | C | 1 | a0001c0001t0001g0090 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.583-1429T>C | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 6/11 | chr17 | 59772325 | |||||||
| chr17:59772335 | C | T | 1 | a0001c0001t0001g0201 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.583-1419C>T | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 6/11 | chr17 | 59772335 | |||||||
| chr17:59772674 | C | CA | 6 | a0001c0001t0002g0192 a0001c0001t0002g0193 a0001c0001t0002g0194 others(3): Show |
6 | HG00741.hp1 HG01069.hp2 HG01071.hp2 others(3): Show |
intron_variant | MODIFIER | c.583-1079dupA | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr17 | 59772674 | ||||||
| chr17:59772890 | C | T | 87 | a0001c0001t0001g0069 a0001c0001t0001g0070 a0001c0001t0001g0100 others(84): Show |
87 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(84): Show |
intron_variant | MODIFIER | c.583-864C>T | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 6/11 | chr17 | 59772890 | |||||||
| chr17:59772950 | C | CT | 58 | a0001c0001t0001g0069 a0001c0001t0001g0070 a0001c0001t0001g0100 others(55): Show |
58 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(55): Show |
intron_variant | MODIFIER | c.583-774dupT | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr17 | 59772950 | ||||||
| chr17:59772950 | C | CTT | 35 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(32): Show |
35 | HG00140.hp2 HG00642.hp2 HG01074.hp2 others(32): Show |
intron_variant | MODIFIER | c.583-775_583-774dup others(2): Show |
VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr17 | 59772950 | ||||||
| chr17:59772950 | C | CTTT | 7 | a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0206 others(4): Show |
7 | HG00621.hp2 HG01952.hp2 HG02027.hp2 others(4): Show |
intron_variant | MODIFIER | c.583-776_583-774dup others(3): Show |
VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr17 | 59772950 | ||||||
| chr17:59772950 | C | CTTTTTTT others(3): Show |
1 | a0001c0001t0003g0111 | 1 | HG01071.hp1 | intron_variant | MODIFIER | c.583-783_583-774dup others(10): Show |
VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr17 | 59772950 | ||||||
| chr17:59772950 | C | CTTTTTTT others(4): Show |
2 | a0001c0001t0001g0095 a0001c0001t0003g0112 |
2 | HG03471.hp1 HG03834.hp1 |
intron_variant | MODIFIER | c.583-784_583-774dup others(11): Show |
VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr17 | 59772950 | ||||||
| chr17:59772950 | C | CTTTTTTT others(7): Show |
1 | a0001c0001t0003g0118 | 1 | NA19086.hp2 | intron_variant | MODIFIER | c.583-787_583-774dup others(14): Show |
VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr17 | 59772950 | ||||||
| chr17:59772950 | C | CTTTTTTT others(8): Show |
8 | a0001c0001t0001g0139 a0001c0001t0003g0110 a0001c0001t0003g0121 others(5): Show |
8 | HG00673.hp2 HG01978.hp1 HG02015.hp1 others(5): Show |
intron_variant | MODIFIER | c.583-788_583-774dup others(15): Show |
VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr17 | 59772950 | ||||||
| chr17:59772950 | C | CTTTTTTT others(9): Show |
9 | a0001c0001t0001g0132 a0001c0001t0003g0114 a0001c0001t0003g0115 others(6): Show |
9 | HG00738.hp2 HG01069.hp1 HG01261.hp1 others(6): Show |
intron_variant | MODIFIER | c.583-789_583-774dup others(16): Show |
VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr17 | 59772950 | ||||||
| chr17:59772950 | C | CTTTTTTT others(10): Show |
4 | a0001c0001t0003g0105 a0001c0001t0003g0117 a0001c0001t0003g0128 others(1): Show |
4 | HG02647.hp1 HG02717.hp1 NA18966.hp1 others(1): Show |
intron_variant | MODIFIER | c.583-790_583-774dup others(17): Show |
VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr17 | 59772950 | ||||||
| chr17:59772950 | C | CTTTTTTT others(11): Show |
1 | a0001c0001t0003g0138 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.583-791_583-774dup others(18): Show |
VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr17 | 59772950 | ||||||
| chr17:59772950 | C | CTTTTTTT others(12): Show |
2 | a0001c0001t0003g0136 a0001c0001t0003g0141 |
2 | HG00438.hp2 NA18959.hp2 |
intron_variant | MODIFIER | c.583-792_583-774dup others(19): Show |
VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr17 | 59772950 | ||||||
| chr17:59772950 | C | CTTTTTTT others(13): Show |
2 | a0001c0001t0003g0135 a0001c0001t0003g0147 |
2 | NA18967.hp2 NA18992.hp2 |
intron_variant | MODIFIER | c.583-793_583-774dup others(20): Show |
VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr17 | 59772950 | ||||||
| chr17:59772950 | C | CTTTTTTT others(15): Show |
2 | a0001c0001t0003g0108 a0001c0001t0003g0126 |
2 | HG03927.hp2 NA19056.hp1 |
intron_variant | MODIFIER | c.583-795_583-774dup others(22): Show |
VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr17 | 59772950 | ||||||
| chr17:59772950 | C | CTTTTTTT others(16): Show |
4 | a0001c0001t0003g0122 a0001c0001t0003g0142 a0001c0001t0003g0259 others(1): Show |
4 | HG02896.hp2 NA18987.hp1 NA19080.hp2 others(1): Show |
intron_variant | MODIFIER | c.583-796_583-774dup others(23): Show |
VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr17 | 59772950 | ||||||
| chr17:59772950 | C | CTTTTTTT others(18): Show |
1 | a0001c0001t0003g0143 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.583-798_583-774dup others(25): Show |
VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr17 | 59772950 | ||||||
| chr17:59772950 | C | CTTTTTTT others(19): Show |
1 | a0001c0001t0003g0116 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.583-799_583-774dup others(26): Show |
VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr17 | 59772950 | ||||||
| chr17:59772950 | C | CTTTTTTT others(21): Show |
1 | a0001c0001t0003g0261 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.583-801_583-774dup others(28): Show |
VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr17 | 59772950 | ||||||
| chr17:59772950 | C | CTTTTTTT others(23): Show |
1 | a0001c0001t0003g0151 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.583-803_583-774dup others(30): Show |
VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr17 | 59772950 | ||||||
| chr17:59772950 | C | CTTTTTTT others(24): Show |
1 | a0001c0001t0003g0258 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.583-774_583-773ins others(31): Show |
VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr17 | 59772950 | ||||||
| chr17:59772950 | CTTTTTTT | C | 12 | a0001c0001t0001g0277 a0001c0001t0002g0026 a0001c0001t0002g0034 others(9): Show |
12 | HG00621.hp1 HG01168.hp2 HG02027.hp1 others(9): Show |
intron_variant | MODIFIER | c.583-780_583-774del others(7): Show |
VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr17 | 59772950 | ||||||
| chr17:59772950 | CTTTTTTT others(1): Show |
C | 96 | a0001c0001t0001g0003 a0001c0001t0001g0076 a0001c0001t0001g0077 others(93): Show |
96 | HG00408.hp2 HG00423.hp2 HG00544.hp1 others(93): Show |
intron_variant | MODIFIER | c.583-781_583-774del others(8): Show |
VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr17 | 59772950 | ||||||
| chr17:59772950 | CTTTTTTT others(16): Show |
C | 1 | a0001c0001t0003g0133 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.583-796_583-774del others(23): Show |
VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr17 | 59772950 | ||||||
| chr17:59772993 | T | G | 1 | a0001c0001t0004g0272 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.583-761T>G | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 6/11 | chr17 | 59772993 | |||||||
| chr17:59773047 | C | T | 2 | a0001c0001t0001g0011 a0001c0001t0001g0179 |
2 | HG00423.hp1 HG01952.hp2 |
intron_variant | MODIFIER | c.583-707C>T | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 6/11 | chr17 | 59773047 | |||||||
| chr17:59773048 | G | A | 1 | a0001c0001t0001g0222 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.583-706G>A | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 6/11 | chr17 | 59773048 | |||||||
| chr17:59773181 | C | T | 3 | a0001c0001t0002g0013 a0001c0001t0002g0023 a0001c0001t0002g0071 |
3 | HG02735.hp1 HG03688.hp2 NA20752.hp2 |
intron_variant | MODIFIER | c.583-573C>T | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 6/11 | chr17 | 59773181 | |||||||
| chr17:59773190 | G | A | 21 | a0001c0001t0001g0003 a0001c0001t0001g0076 a0001c0001t0001g0077 others(18): Show |
21 | HG01243.hp1 HG01891.hp2 HG02257.hp1 others(18): Show |
intron_variant | MODIFIER | c.583-564G>A | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 6/11 | chr17 | 59773190 | |||||||
| chr17:59773304 | T | TG | 27 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(24): Show |
27 | HG01099.hp1 HG01109.hp2 HG01884.hp1 others(24): Show |
intron_variant | MODIFIER | c.583-441dupG | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr17 | 59773304 | ||||||
| chr17:59773402 | A | AT | 101 | a0001c0001t0001g0003 a0001c0001t0001g0076 a0001c0001t0001g0077 others(98): Show |
101 | HG00408.hp2 HG00423.hp2 HG00544.hp1 others(98): Show |
intron_variant | MODIFIER | c.583-339dupT | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr17 | 59773402 | ||||||
| chr17:59773427 | A | C | 1 | a0001c0001t0001g0239 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.583-327A>C | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 6/11 | chr17 | 59773427 | |||||||
| chr17:59773520 | C | T | 1 | a0001c0001t0001g0173 | 1 | NA18993.hp1 | intron_variant | MODIFIER | c.583-234C>T | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 6/11 | chr17 | 59773520 | |||||||
| chr17:59773606 | T | C | 1 | a0001c0001t0003g0118 | 1 | NA19086.hp2 | intron_variant | MODIFIER | c.583-148T>C | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 6/11 | chr17 | 59773606 | |||||||
| chr17:59774379 | C | T | 1 | a0001c0001t0002g0043 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.714+494C>T | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 7/11 | chr17 | 59774379 | |||||||
| chr17:59774412 | TA | T | 87 | a0001c0001t0001g0069 a0001c0001t0001g0070 a0001c0001t0001g0100 others(84): Show |
87 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(84): Show |
intron_variant | MODIFIER | c.714+539delA | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr17 | 59774412 | ||||||
| chr17:59774420 | A | T | 87 | a0001c0001t0001g0069 a0001c0001t0001g0070 a0001c0001t0001g0100 others(84): Show |
87 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(84): Show |
intron_variant | MODIFIER | c.714+535A>T | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 7/11 | chr17 | 59774420 | |||||||
| chr17:59774421 | AAAAGAAA others(1): Show |
A | 78 | a0001c0001t0002g0012 a0001c0001t0002g0013 a0001c0001t0002g0014 others(75): Show |
78 | HG00408.hp2 HG00423.hp2 HG00544.hp1 others(75): Show |
intron_variant | MODIFIER | c.714+552_714+559del others(8): Show |
VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr17 | 59774421 | ||||||
| chr17:59774933 | CA | C | 8 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(5): Show |
8 | HG01099.hp1 HG01884.hp1 HG01952.hp2 others(5): Show |
intron_variant | MODIFIER | c.714+1056delA | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr17 | 59774933 | ||||||
| chr17:59774941 | AT | A | 149 | a0001c0001t0001g0069 a0001c0001t0001g0070 a0001c0001t0001g0095 others(146): Show |
149 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(146): Show |
intron_variant | MODIFIER | c.714+1074delT | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr17 | 59774941 | ||||||
| chr17:59774942 | T | A | 100 | a0001c0001t0001g0003 a0001c0001t0001g0076 a0001c0001t0001g0077 others(97): Show |
100 | HG00408.hp2 HG00423.hp2 HG00544.hp1 others(97): Show |
intron_variant | MODIFIER | c.714+1057T>A | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 7/11 | chr17 | 59774942 | |||||||
| chr17:59774943 | T | A | 3 | a0001c0001t0001g0084 a0001c0001t0001g0089 a0001c0001t0002g0053 |
3 | HG02486.hp2 HG06807.hp1 NA19086.hp1 |
intron_variant | MODIFIER | c.714+1058T>A | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 7/11 | chr17 | 59774943 | |||||||
| chr17:59775087 | G | A | 1 | a0001c0001t0001g0230 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.714+1202G>A | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 7/11 | chr17 | 59775087 | |||||||
| chr17:59775224 | G | A | 1 | a0001c0001t0001g0229 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.714+1339G>A | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 7/11 | chr17 | 59775224 | |||||||
| chr17:59775278 | A | T | 1 | a0001c0001t0001g0218 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.714+1393A>T | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 7/11 | chr17 | 59775278 | |||||||
| chr17:59775283 | C | T | 3 | a0001c0001t0003g0131 a0001c0001t0003g0134 a0001c0001t0003g0146 |
3 | HG02895.hp1 HG03579.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.714+1398C>T | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 7/11 | chr17 | 59775283 | |||||||
| chr17:59775306 | T | C | 1 | a0001c0001t0003g0259 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.714+1421T>C | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 7/11 | chr17 | 59775306 | |||||||
| chr17:59775369 | T | C | 8 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(5): Show |
8 | HG01099.hp1 HG01884.hp1 HG01952.hp2 others(5): Show |
intron_variant | MODIFIER | c.714+1484T>C | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 7/11 | chr17 | 59775369 | |||||||
| chr17:59775796 | A | G | 1 | a0001c0001t0004g0268 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.714+1911A>G | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 7/11 | chr17 | 59775796 | |||||||
| chr17:59775853 | A | C | 165 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(162): Show |
165 | HG00408.hp2 HG00423.hp2 HG00438.hp2 others(162): Show |
intron_variant | MODIFIER | c.714+1968A>C | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 7/11 | chr17 | 59775853 | |||||||
| chr17:59775854 | G | A | 1 | a0001c0001t0001g0009 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.714+1969G>A | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 7/11 | chr17 | 59775854 | |||||||
| chr17:59776210 | TAAAA | T | 62 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(59): Show |
62 | HG00438.hp2 HG00642.hp1 HG00673.hp2 others(59): Show |
intron_variant | MODIFIER | c.714+2331_714+2334d others(6): Show |
VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr17 | 59776210 | ||||||
| chr17:59776314 | A | C | 1 | a0001c0001t0003g0107 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.714+2429A>C | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 7/11 | chr17 | 59776314 | |||||||
| chr17:59776341 | T | C | 266 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(263): Show |
266 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(263): Show |
intron_variant | MODIFIER | c.714+2456T>C | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 7/11 | chr17 | 59776341 | |||||||
| chr17:59776796 | G | A | 1 | a0001c0001t0001g0089 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.714+2911G>A | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 7/11 | chr17 | 59776796 | |||||||
| chr17:59776905 | T | C | 8 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(5): Show |
8 | HG01099.hp1 HG01884.hp1 HG01952.hp2 others(5): Show |
intron_variant | MODIFIER | c.714+3020T>C | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 7/11 | chr17 | 59776905 | |||||||
| chr17:59777059 | G | A | 266 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(263): Show |
266 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(263): Show |
intron_variant | MODIFIER | c.714+3174G>A | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 7/11 | chr17 | 59777059 | |||||||
| chr17:59777249 | G | A | 2 | a0001c0001t0001g0077 a0001c0001t0001g0278 |
2 | HG02258.hp2 HG02630.hp1 |
intron_variant | MODIFIER | c.714+3364G>A | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 7/11 | chr17 | 59777249 | |||||||
| chr17:59777422 | C | T | 103 | a0001c0001t0001g0003 a0001c0001t0001g0076 a0001c0001t0001g0077 others(100): Show |
103 | HG00408.hp2 HG00423.hp2 HG00544.hp1 others(100): Show |
intron_variant | MODIFIER | c.714+3537C>T | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 7/11 | chr17 | 59777422 | |||||||
| chr17:59777494 | A | G | 53 | a0001c0001t0003g0105 a0001c0001t0003g0107 a0001c0001t0003g0108 others(50): Show |
53 | HG00438.hp2 HG00642.hp1 HG00673.hp2 others(50): Show |
intron_variant | MODIFIER | c.714+3609A>G | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 7/11 | chr17 | 59777494 | |||||||
| chr17:59777731 | G | A | 21 | a0001c0001t0001g0003 a0001c0001t0001g0076 a0001c0001t0001g0077 others(18): Show |
21 | HG01243.hp1 HG01891.hp2 HG02257.hp1 others(18): Show |
intron_variant | MODIFIER | c.714+3846G>A | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 7/11 | chr17 | 59777731 | |||||||
| chr17:59777788 | T | G | 6 | a0001c0001t0003g0115 a0001c0001t0003g0123 a0001c0001t0003g0124 others(3): Show |
6 | HG00738.hp2 HG01069.hp1 HG01261.hp1 others(3): Show |
intron_variant | MODIFIER | c.714+3903T>G | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 7/11 | chr17 | 59777788 | |||||||
| chr17:59777812 | T | TCAAAA | 61 | a0001c0001t0001g0069 a0001c0001t0001g0070 a0001c0001t0001g0186 others(58): Show |
61 | HG00544.hp1 HG00621.hp1 HG00639.hp2 others(58): Show |
intron_variant | MODIFIER | c.714+3968_714+3972d others(7): Show |
VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr17 | 59777812 | ||||||
| chr17:59777812 | T | TCAAAACA others(3): Show |
16 | a0001c0001t0002g0033 a0001c0001t0002g0035 a0001c0001t0002g0042 others(13): Show |
16 | HG00423.hp2 HG00741.hp1 HG01074.hp1 others(13): Show |
intron_variant | MODIFIER | c.714+3963_714+3972d others(12): Show |
VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr17 | 59777812 | ||||||
| chr17:59777812 | TCAAAA | T | 61 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(58): Show |
61 | HG00423.hp1 HG00642.hp1 HG00673.hp1 others(58): Show |
intron_variant | MODIFIER | c.714+3968_714+3972d others(7): Show |
VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr17 | 59777812 | ||||||
| chr17:59777812 | TCAAAACA others(3): Show |
T | 10 | a0001c0001t0001g0009 a0001c0001t0001g0241 a0001c0001t0001g0255 others(7): Show |
10 | HG02109.hp1 HG02145.hp1 HG02145.hp2 others(7): Show |
intron_variant | MODIFIER | c.714+3963_714+3972d others(12): Show |
VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr17 | 59777812 | ||||||
| chr17:59777812 | TCAAAACA others(8): Show |
T | 1 | a0001c0001t0001g0200 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.714+3958_714+3972d others(17): Show |
VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr17 | 59777812 | ||||||
| chr17:59777812 | TCAAAACA others(13): Show |
T | 1 | a0001c0001t0001g0095 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.714+3953_714+3972d others(22): Show |
VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr17 | 59777812 | ||||||
| chr17:59777955 | C | G | 2 | a0001c0001t0007g0274 a0001c0001t0007g0275 |
2 | HG03491.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.714+4070C>G | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 7/11 | chr17 | 59777955 | |||||||
| chr17:59778250 | A | C | 1 | a0001c0001t0002g0068 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.714+4365A>C | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 7/11 | chr17 | 59778250 | |||||||
| chr17:59778263 | C | T | 4 | a0001c0001t0005g0002 a0001c0001t0005g0018 a0001c0001t0005g0058 others(1): Show |
4 | HG02698.hp2 HG02738.hp1 HG03927.hp1 others(1): Show |
intron_variant | MODIFIER | c.714+4378C>T | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 7/11 | chr17 | 59778263 | |||||||
| chr17:59778289 | C | A | 2 | a0001c0001t0006g0285 a0001c0001t0006g0286 |
2 | HG02109.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.714+4404C>A | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 7/11 | chr17 | 59778289 | |||||||
| chr17:59778498 | G | A | 1 | a0001c0001t0002g0049 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.714+4613G>A | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 7/11 | chr17 | 59778498 | |||||||
| chr17:59778540 | CA | C | 173 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(170): Show |
173 | HG00408.hp2 HG00423.hp2 HG00438.hp2 others(170): Show |
intron_variant | MODIFIER | c.714+4671delA | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr17 | 59778540 | ||||||
| chr17:59778549 | A | G | 5 | a0001c0001t0003g0154 a0001c0001t0003g0155 a0001c0001t0003g0156 others(2): Show |
5 | HG01168.hp2 HG02486.hp1 HG02615.hp2 others(2): Show |
intron_variant | MODIFIER | c.714+4664A>G | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 7/11 | chr17 | 59778549 | |||||||
| chr17:59779268 | A | G | 8 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(5): Show |
8 | HG01099.hp1 HG01884.hp1 HG01952.hp2 others(5): Show |
intron_variant | MODIFIER | c.714+5383A>G | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 7/11 | chr17 | 59779268 | |||||||
| chr17:59779398 | G | A | 1 | a0001c0001t0001g0218 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.714+5513G>A | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 7/11 | chr17 | 59779398 | |||||||
| chr17:59779918 | G | C | 2 | a0001c0001t0001g0132 a0001c0001t0001g0139 |
2 | HG02698.hp1 HG04199.hp2 |
intron_variant | MODIFIER | c.714+6033G>C | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 7/11 | chr17 | 59779918 | |||||||
| chr17:59779926 | T | C | 1 | a0001c0001t0001g0168 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.714+6041T>C | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 7/11 | chr17 | 59779926 | |||||||
| chr17:59780113 | T | G | 2 | a0001c0001t0002g0012 a0001c0001t0002g0019 |
2 | HG00738.hp1 HG03654.hp1 |
intron_variant | MODIFIER | c.714+6228T>G | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 7/11 | chr17 | 59780113 | |||||||
| chr17:59780329 | G | A | 1 | a0001c0001t0001g0204 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.714+6444G>A | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 7/11 | chr17 | 59780329 | |||||||
| chr17:59780779 | G | A | 1 | a0001c0001t0001g0176 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.714+6894G>A | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 7/11 | chr17 | 59780779 | |||||||
| chr17:59780824 | G | T | 1 | a0001c0001t0001g0239 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.714+6939G>T | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 7/11 | chr17 | 59780824 | |||||||
| chr17:59781013 | A | T | 78 | a0001c0001t0002g0012 a0001c0001t0002g0013 a0001c0001t0002g0014 others(75): Show |
78 | HG00408.hp2 HG00423.hp2 HG00544.hp1 others(75): Show |
intron_variant | MODIFIER | c.714+7128A>T | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 7/11 | chr17 | 59781013 | |||||||
| chr17:59781345 | C | T | 4 | a0001c0001t0001g0207 a0001c0001t0001g0211 a0001c0001t0001g0218 others(1): Show |
4 | HG00280.hp2 HG00639.hp1 HG01255.hp2 others(1): Show |
intron_variant | MODIFIER | c.714+7460C>T | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 7/11 | chr17 | 59781345 | |||||||
| chr17:59781445 | A | G | 11 | a0001c0001t0004g0262 a0001c0001t0004g0263 a0001c0001t0004g0265 others(8): Show |
11 | HG01109.hp2 HG02615.hp1 HG02896.hp1 others(8): Show |
intron_variant | MODIFIER | c.714+7560A>G | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 7/11 | chr17 | 59781445 | |||||||
| chr17:59781615 | T | A | 5 | a0001c0001t0003g0154 a0001c0001t0003g0155 a0001c0001t0003g0156 others(2): Show |
5 | HG01168.hp2 HG02486.hp1 HG02615.hp2 others(2): Show |
intron_variant | MODIFIER | c.714+7730T>A | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 7/11 | chr17 | 59781615 | |||||||
| chr17:59781637 | C | T | 1 | a0001c0001t0001g0095 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.714+7752C>T | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 7/11 | chr17 | 59781637 | |||||||
| chr17:59781763 | A | T | 1 | a0001c0001t0001g0208 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.714+7878A>T | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 7/11 | chr17 | 59781763 | |||||||
| chr17:59781849 | G | A | 89 | a0001c0001t0001g0069 a0001c0001t0001g0070 a0001c0001t0001g0100 others(86): Show |
89 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(86): Show |
intron_variant | MODIFIER | c.714+7964G>A | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 7/11 | chr17 | 59781849 | |||||||
| chr17:59782096 | A | G | 2 | a0001c0001t0001g0076 a0001c0001t0001g0082 |
2 | HG02559.hp1 HG02717.hp2 |
intron_variant | MODIFIER | c.714+8211A>G | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 7/11 | chr17 | 59782096 | |||||||
| chr17:59782300 | CTTTT | C | 54 | a0001c0001t0001g0277 a0001c0001t0003g0105 a0001c0001t0003g0107 others(51): Show |
54 | HG00438.hp2 HG00642.hp1 HG00673.hp2 others(51): Show |
intron_variant | MODIFIER | c.714+8418_714+8421d others(6): Show |
VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr17 | 59782300 | ||||||
| chr17:59782344 | C | T | 78 | a0001c0001t0002g0012 a0001c0001t0002g0013 a0001c0001t0002g0014 others(75): Show |
78 | HG00408.hp2 HG00423.hp2 HG00544.hp1 others(75): Show |
intron_variant | MODIFIER | c.714+8459C>T | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 7/11 | chr17 | 59782344 | |||||||
| chr17:59782598 | C | T | 11 | a0001c0001t0004g0262 a0001c0001t0004g0263 a0001c0001t0004g0265 others(8): Show |
11 | HG01109.hp2 HG02615.hp1 HG02896.hp1 others(8): Show |
intron_variant | MODIFIER | c.714+8713C>T | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 7/11 | chr17 | 59782598 | |||||||
| chr17:59782599 | G | A | 1 | a0001c0001t0001g0095 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.714+8714G>A | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 7/11 | chr17 | 59782599 | |||||||
| chr17:59782681 | G | A | 2 | a0001c0001t0001g0077 a0001c0001t0001g0278 |
2 | HG02258.hp2 HG02630.hp1 |
intron_variant | MODIFIER | c.714+8796G>A | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 7/11 | chr17 | 59782681 | |||||||
| chr17:59782789 | G | T | 177 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(174): Show |
177 | HG00408.hp2 HG00423.hp2 HG00438.hp2 others(174): Show |
intron_variant | MODIFIER | c.714+8904G>T | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 7/11 | chr17 | 59782789 | |||||||
| chr17:59782792 | G | A | 1 | a0001c0001t0003g0113 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.714+8907G>A | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 7/11 | chr17 | 59782792 | |||||||
| chr17:59782796 | AG | A | 103 | a0001c0001t0001g0003 a0001c0001t0001g0076 a0001c0001t0001g0077 others(100): Show |
103 | HG00408.hp2 HG00423.hp2 HG00544.hp1 others(100): Show |
intron_variant | MODIFIER | c.714+8912delG | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 7/11 | chr17 | 59782796 | |||||||
| chr17:59782867 | T | C | 4 | a0001c0001t0006g0283 a0001c0001t0006g0284 a0001c0001t0006g0285 others(1): Show |
4 | HG02109.hp2 HG03130.hp2 HG06807.hp2 others(1): Show |
intron_variant | MODIFIER | c.714+8982T>C | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 7/11 | chr17 | 59782867 | |||||||
| chr17:59782989 | A | T | 1 | a0001c0001t0001g0200 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.714+9104A>T | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 7/11 | chr17 | 59782989 | |||||||
| chr17:59783001 | C | G | 1 | a0001c0001t0004g0273 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.714+9116C>G | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 7/11 | chr17 | 59783001 | |||||||
| chr17:59783020 | C | T | 18 | a0001c0001t0001g0003 a0001c0001t0001g0076 a0001c0001t0001g0077 others(15): Show |
18 | HG01243.hp1 HG01891.hp2 HG02257.hp1 others(15): Show |
intron_variant | MODIFIER | c.714+9135C>T | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 7/11 | chr17 | 59783020 | |||||||
| chr17:59783064 | C | T | 1 | a0001c0001t0003g0120 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.714+9179C>T | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 7/11 | chr17 | 59783064 | |||||||
| chr17:59783089 | C | T | 1 | a0001c0001t0001g0277 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.714+9204C>T | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 7/11 | chr17 | 59783089 | |||||||
| chr17:59783153 | G | A | 8 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(5): Show |
8 | HG01099.hp1 HG01884.hp1 HG01952.hp2 others(5): Show |
intron_variant | MODIFIER | c.714+9268G>A | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 7/11 | chr17 | 59783153 | |||||||
| chr17:59783322 | G | A | 2 | a0001c0001t0001g0188 a0001c0001t0001g0230 |
2 | HG01074.hp2 HG02280.hp1 |
intron_variant | MODIFIER | c.714+9437G>A | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 7/11 | chr17 | 59783322 | |||||||
| chr17:59783690 | C | T | 1 | a0001c0001t0001g0183 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.714+9805C>T | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 7/11 | chr17 | 59783690 | |||||||
| chr17:59783748 | C | T | 2 | a0001c0001t0003g0134 a0001c0001t0003g0146 |
2 | HG02895.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.714+9863C>T | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 7/11 | chr17 | 59783748 | |||||||
| chr17:59783893 | A | C | 1 | a0001c0001t0001g0006 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.714+10008A>C | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 7/11 | chr17 | 59783893 | |||||||
| chr17:59784100 | AGT | A | 45 | a0001c0001t0001g0104 a0001c0001t0001g0106 a0001c0001t0001g0162 others(42): Show |
45 | HG00408.hp1 HG00438.hp1 HG00642.hp1 others(42): Show |
intron_variant | MODIFIER | c.714+10257_714+1025 others(6): Show |
VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr17 | 59784100 | ||||||
| chr17:59784100 | AGTGT | A | 18 | a0001c0001t0001g0003 a0001c0001t0001g0077 a0001c0001t0001g0153 others(15): Show |
18 | HG00438.hp2 HG01071.hp1 HG01243.hp2 others(15): Show |
intron_variant | MODIFIER | c.714+10255_714+1025 others(8): Show |
VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr17 | 59784100 | ||||||
| chr17:59784100 | AGTGTGTG others(9): Show |
A | 1 | a0001c0001t0003g0260 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.714+10243_714+1025 others(20): Show |
VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr17 | 59784100 | ||||||
| chr17:59784136 | T | A | 1 | a0001c0001t0001g0277 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.714+10251T>A | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 7/11 | chr17 | 59784136 | |||||||
| chr17:59784138 | T | A | 8 | a0001c0001t0001g0011 a0001c0001t0001g0106 a0001c0001t0001g0225 others(5): Show |
8 | HG00408.hp1 HG00673.hp2 HG01952.hp2 others(5): Show |
intron_variant | MODIFIER | c.714+10253T>A | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 7/11 | chr17 | 59784138 | |||||||
| chr17:59784138 | T | TGAGA | 7 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(4): Show |
7 | HG01099.hp1 HG02886.hp1 HG02886.hp2 others(4): Show |
intron_variant | MODIFIER | c.714+10254_714+1025 others(8): Show |
VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr17 | 59784138 | ||||||
| chr17:59784138 | TGTGTGA | T | 3 | a0001c0001t0001g0280 a0001c0001t0008g0279 a0001c0001t0008g0281 |
3 | HG02145.hp2 HG02818.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.714+10255_714+1026 others(10): Show |
VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr17 | 59784138 | ||||||
| chr17:59784140 | T | A | 130 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(127): Show |
130 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(127): Show |
intron_variant | MODIFIER | c.714+10255T>A | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 7/11 | chr17 | 59784140 | |||||||
| chr17:59784140 | T | TGA | 8 | a0001c0001t0001g0069 a0001c0001t0001g0070 a0001c0001t0001g0132 others(5): Show |
8 | HG00621.hp2 HG01069.hp1 HG02698.hp1 others(5): Show |
intron_variant | MODIFIER | c.714+10256_714+1025 others(6): Show |
VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr17 | 59784140 | ||||||
| chr17:59784140 | T | TGAGAGAG others(1): Show |
5 | a0001c0001t0004g0262 a0001c0001t0004g0263 a0001c0001t0004g0269 others(2): Show |
5 | HG01109.hp2 HG03041.hp2 HG03486.hp2 others(2): Show |
intron_variant | MODIFIER | c.714+10256_714+1025 others(12): Show |
VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr17 | 59784140 | ||||||
| chr17:59784142 | T | A | 164 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(161): Show |
164 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(161): Show |
intron_variant | MODIFIER | c.714+10257T>A | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 7/11 | chr17 | 59784142 | |||||||
| chr17:59784142 | T | TGA | 11 | a0001c0001t0001g0081 a0001c0001t0001g0083 a0001c0001t0001g0088 others(8): Show |
11 | HG00544.hp1 HG01358.hp1 HG01891.hp2 others(8): Show |
intron_variant | MODIFIER | c.714+10272_714+1027 others(6): Show |
VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr17 | 59784142 | ||||||
| chr17:59784142 | T | TGAGA | 6 | a0001c0001t0001g0176 a0001c0001t0001g0181 a0001c0001t0001g0219 others(3): Show |
6 | HG02083.hp1 HG02109.hp2 HG02451.hp1 others(3): Show |
intron_variant | MODIFIER | c.714+10270_714+1027 others(8): Show |
VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr17 | 59784142 | ||||||
| chr17:59784142 | T | TGAGAGAG others(1): Show |
5 | a0001c0001t0001g0009 a0001c0001t0004g0265 a0001c0001t0004g0266 others(2): Show |
5 | HG02615.hp1 HG02965.hp2 HG02970.hp1 others(2): Show |
intron_variant | MODIFIER | c.714+10266_714+1027 others(12): Show |
VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr17 | 59784142 | ||||||
| chr17:59784142 | T | TGTGA | 26 | a0001c0001t0002g0015 a0001c0001t0002g0016 a0001c0001t0002g0017 others(23): Show |
26 | HG00423.hp2 HG00741.hp1 HG01069.hp2 others(23): Show |
intron_variant | MODIFIER | c.714+10258_714+1025 others(8): Show |
VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr17 | 59784142 | ||||||
| chr17:59784142 | T | TGTGAGAG others(5): Show |
1 | a0001c0001t0004g0267 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.714+10258_714+1025 others(16): Show |
VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr17 | 59784142 | ||||||
| chr17:59784142 | T | TGTGTGA | 19 | a0001c0001t0002g0012 a0001c0001t0002g0013 a0001c0001t0002g0014 others(16): Show |
19 | HG00408.hp2 HG00738.hp1 HG01074.hp1 others(16): Show |
intron_variant | MODIFIER | c.714+10258_714+1025 others(10): Show |
VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr17 | 59784142 | ||||||
| chr17:59784142 | T | TGTGTGTG others(1): Show |
17 | a0001c0001t0002g0023 a0001c0001t0002g0033 a0001c0001t0002g0034 others(14): Show |
17 | HG00621.hp1 HG00639.hp2 HG00673.hp1 others(14): Show |
intron_variant | MODIFIER | c.714+10258_714+1025 others(12): Show |
VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr17 | 59784142 | ||||||
| chr17:59784142 | T | TGTGTGTG others(3): Show |
1 | a0001c0001t0005g0018 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.714+10258_714+1025 others(14): Show |
VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr17 | 59784142 | ||||||
| chr17:59784142 | T | TGTGTGTG others(7): Show |
1 | a0001c0001t0002g0022 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.714+10258_714+1025 others(18): Show |
VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr17 | 59784142 | ||||||
| chr17:59784144 | A | T | 1 | a0001c0001t0001g0095 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.714+10259A>T | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 7/11 | chr17 | 59784144 | |||||||
| chr17:59784146 | A | T | 1 | a0001c0001t0001g0095 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.714+10261A>T | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 7/11 | chr17 | 59784146 | |||||||
| chr17:59784247 | T | G | 1 | a0001c0001t0003g0110 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.714+10362T>G | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 7/11 | chr17 | 59784247 | |||||||
| chr17:59784280 | C | T | 1 | a0001c0001t0002g0236 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.714+10395C>T | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 7/11 | chr17 | 59784280 | |||||||
| chr17:59784380 | C | A | 1 | a0001c0001t0003g0110 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.714+10495C>A | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 7/11 | chr17 | 59784380 | |||||||
| chr17:59784405 | C | A | 2 | a0001c0001t0001g0204 a0001c0001t0001g0238 |
2 | HG02922.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.714+10520C>A | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 7/11 | chr17 | 59784405 | |||||||
| chr17:59784425 | C | T | 18 | a0001c0001t0001g0003 a0001c0001t0001g0076 a0001c0001t0001g0077 others(15): Show |
18 | HG01243.hp1 HG01891.hp2 HG02257.hp1 others(15): Show |
intron_variant | MODIFIER | c.714+10540C>T | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 7/11 | chr17 | 59784425 | |||||||
| chr17:59784433 | A | C | 53 | a0001c0001t0003g0105 a0001c0001t0003g0107 a0001c0001t0003g0108 others(50): Show |
53 | HG00438.hp2 HG00642.hp1 HG00673.hp2 others(50): Show |
intron_variant | MODIFIER | c.714+10548A>C | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 7/11 | chr17 | 59784433 | |||||||
| chr17:59784621 | C | G | 1 | a0001c0001t0001g0089 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.714+10736C>G | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 7/11 | chr17 | 59784621 | |||||||
| chr17:59784634 | G | A | 62 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(59): Show |
62 | HG00438.hp2 HG00642.hp1 HG00673.hp2 others(59): Show |
intron_variant | MODIFIER | c.714+10749G>A | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 7/11 | chr17 | 59784634 | |||||||
| chr17:59785159 | A | G | 3 | a0001c0001t0003g0154 a0001c0001t0003g0156 a0001c0001t0003g0264 |
3 | HG01168.hp2 HG02970.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.714+11274A>G | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 7/11 | chr17 | 59785159 | |||||||
| chr17:59785231 | T | C | 266 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(263): Show |
266 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(263): Show |
intron_variant | MODIFIER | c.714+11346T>C | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 7/11 | chr17 | 59785231 | |||||||
| chr17:59785597 | C | T | 1 | a0001c0001t0002g0072 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.714+11712C>T | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 7/11 | chr17 | 59785597 | |||||||
| chr17:59785598 | G | A | 8 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(5): Show |
8 | HG01099.hp1 HG01884.hp1 HG01952.hp2 others(5): Show |
intron_variant | MODIFIER | c.714+11713G>A | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 7/11 | chr17 | 59785598 | |||||||
| chr17:59785613 | C | A | 1 | a0001c0001t0001g0095 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.714+11728C>A | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 7/11 | chr17 | 59785613 | |||||||
| chr17:59785622 | A | G | 1 | a0001c0001t0003g0121 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.714+11737A>G | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 7/11 | chr17 | 59785622 | |||||||
| chr17:59785689 | C | CA | 11 | a0001c0001t0001g0150 a0001c0001t0001g0163 a0001c0001t0001g0176 others(8): Show |
11 | HG01256.hp1 HG02109.hp2 HG03130.hp2 others(8): Show |
intron_variant | MODIFIER | c.714+11822dupA | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr17 | 59785689 | ||||||
| chr17:59785689 | CA | C | 6 | a0001c0001t0001g0007 a0001c0001t0001g0103 a0001c0001t0001g0203 others(3): Show |
6 | HG01099.hp1 HG01884.hp2 HG02738.hp2 others(3): Show |
intron_variant | MODIFIER | c.714+11822delA | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr17 | 59785689 | ||||||
| chr17:59786099 | A | G | 1 | a0001c0001t0001g0225 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.714+12214A>G | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 7/11 | chr17 | 59786099 | |||||||
| chr17:59786136 | A | G | 5 | a0001c0001t0002g0024 a0001c0001t0002g0025 a0001c0001t0002g0026 others(2): Show |
5 | NA18977.hp2 NA19057.hp2 NA19060.hp1 others(2): Show |
intron_variant | MODIFIER | c.714+12251A>G | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 7/11 | chr17 | 59786136 | |||||||
| chr17:59786351 | C | T | 8 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(5): Show |
8 | HG01099.hp1 HG01884.hp1 HG01952.hp2 others(5): Show |
intron_variant | MODIFIER | c.714+12466C>T | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 7/11 | chr17 | 59786351 | |||||||
| chr17:59786732 | G | A | 1 | a0001c0001t0001g0222 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.714+12847G>A | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 7/11 | chr17 | 59786732 | |||||||
| chr17:59787391 | T | G | 2 | a0001c0001t0002g0020 a0001c0001t0002g0028 |
2 | HG01123.hp1 HG01168.hp1 |
intron_variant | MODIFIER | c.714+13506T>G | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 7/11 | chr17 | 59787391 | |||||||
| chr17:59787459 | G | A | 2 | a0001c0001t0004g0269 a0001c0001t0004g0270 |
2 | HG03041.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.714+13574G>A | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 7/11 | chr17 | 59787459 | |||||||
| chr17:59787479 | G | T | 5 | a0001c0001t0002g0192 a0001c0001t0002g0193 a0001c0001t0002g0196 others(2): Show |
5 | HG00741.hp1 HG01069.hp2 HG01071.hp2 others(2): Show |
intron_variant | MODIFIER | c.714+13594G>T | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 7/11 | chr17 | 59787479 | |||||||
| chr17:59787584 | G | T | 2 | a0001c0001t0004g0269 a0001c0001t0004g0270 |
2 | HG03041.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.714+13699G>T | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 7/11 | chr17 | 59787584 | |||||||
| chr17:59787710 | A | G | 18 | a0001c0001t0001g0003 a0001c0001t0001g0076 a0001c0001t0001g0077 others(15): Show |
18 | HG01243.hp1 HG01891.hp2 HG02257.hp1 others(15): Show |
intron_variant | MODIFIER | c.714+13825A>G | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 7/11 | chr17 | 59787710 | |||||||
| chr17:59787747 | G | A | 1 | a0001c0001t0001g0254 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.714+13862G>A | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 7/11 | chr17 | 59787747 | |||||||
| chr17:59787757 | G | T | 19 | a0001c0001t0001g0003 a0001c0001t0001g0076 a0001c0001t0001g0077 others(16): Show |
19 | HG01243.hp1 HG01891.hp2 HG02257.hp1 others(16): Show |
intron_variant | MODIFIER | c.714+13872G>T | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 7/11 | chr17 | 59787757 | |||||||
| chr17:59787870 | ACT | A | 11 | a0001c0001t0004g0262 a0001c0001t0004g0263 a0001c0001t0004g0265 others(8): Show |
11 | HG01109.hp2 HG02615.hp1 HG02896.hp1 others(8): Show |
intron_variant | MODIFIER | c.714+13987_714+1398 others(6): Show |
VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr17 | 59787870 | ||||||
| chr17:59787906 | A | G | 1 | a0001c0001t0002g0063 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.714+14021A>G | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 7/11 | chr17 | 59787906 | |||||||
| chr17:59788131 | G | A | 1 | a0001c0001t0001g0095 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.714+14246G>A | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 7/11 | chr17 | 59788131 | |||||||
| chr17:59788267 | T | C | 1 | a0001c0001t0001g0277 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.714+14382T>C | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 7/11 | chr17 | 59788267 | |||||||
| chr17:59788558 | C | CT | 11 | a0001c0001t0004g0262 a0001c0001t0004g0263 a0001c0001t0004g0265 others(8): Show |
11 | HG01109.hp2 HG02615.hp1 HG02896.hp1 others(8): Show |
intron_variant | MODIFIER | c.714+14676dupT | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr17 | 59788558 | ||||||
| chr17:59788777 | G | T | 6 | a0001c0001t0003g0154 a0001c0001t0003g0155 a0001c0001t0003g0156 others(3): Show |
6 | HG01168.hp2 HG02027.hp2 HG02486.hp1 others(3): Show |
intron_variant | MODIFIER | c.714+14892G>T | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 7/11 | chr17 | 59788777 | |||||||
| chr17:59788804 | T | TA | 74 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(71): Show |
74 | HG00438.hp2 HG00642.hp1 HG00673.hp2 others(71): Show |
intron_variant | MODIFIER | c.714+14934dupA | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr17 | 59788804 | ||||||
| chr17:59788804 | T | TAA | 98 | a0001c0001t0001g0003 a0001c0001t0001g0076 a0001c0001t0001g0077 others(95): Show |
98 | HG00408.hp2 HG00423.hp2 HG00544.hp1 others(95): Show |
intron_variant | MODIFIER | c.714+14933_714+1493 others(6): Show |
VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr17 | 59788804 | ||||||
| chr17:59788820 | G | A | 1 | a0001c0001t0002g0020 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.714+14935G>A | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 7/11 | chr17 | 59788820 | |||||||
| chr17:59788941 | C | CT | 20 | a0001c0001t0001g0003 a0001c0001t0001g0076 a0001c0001t0001g0077 others(17): Show |
20 | HG01243.hp1 HG01891.hp2 HG02257.hp1 others(17): Show |
intron_variant | MODIFIER | c.714+15069dupT | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr17 | 59788941 | ||||||
| chr17:59789027 | A | ATGCCTGT others(13): Show |
1 | a0001c0001t0001g0231 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.714+15145_714+1516 others(24): Show |
VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr17 | 59789027 | ||||||
| chr17:59789061 | A | C | 264 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(261): Show |
264 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(261): Show |
intron_variant | MODIFIER | c.714+15176A>C | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 7/11 | chr17 | 59789061 | |||||||
| chr17:59789167 | G | A | 1 | a0001c0001t0001g0208 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.714+15282G>A | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 7/11 | chr17 | 59789167 | |||||||
| chr17:59789305 | C | T | 7 | a0001c0001t0004g0262 a0001c0001t0004g0263 a0001c0001t0004g0267 others(4): Show |
7 | HG01109.hp2 HG02896.hp1 HG03041.hp2 others(4): Show |
intron_variant | MODIFIER | c.714+15420C>T | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 7/11 | chr17 | 59789305 | |||||||
| chr17:59789361 | C | T | 4 | a0001c0001t0001g0175 a0001c0001t0001g0220 a0001c0001t0001g0225 others(1): Show |
4 | HG00642.hp2 HG01978.hp2 HG01981.hp1 others(1): Show |
intron_variant | MODIFIER | c.714+15476C>T | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 7/11 | chr17 | 59789361 | |||||||
| chr17:59789575 | A | G | 1 | a0001c0001t0001g0277 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.714+15690A>G | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 7/11 | chr17 | 59789575 | |||||||
| chr17:59789585 | T | C | 1 | a0001c0001t0001g0277 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.714+15700T>C | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 7/11 | chr17 | 59789585 | |||||||
| chr17:59789610 | A | G | 1 | a0001c0001t0001g0277 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.714+15725A>G | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 7/11 | chr17 | 59789610 | |||||||
| chr17:59789644 | G | A | 1 | a0001c0001t0001g0169 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.714+15759G>A | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 7/11 | chr17 | 59789644 | |||||||
| chr17:59789645 | T | A | 1 | a0001c0001t0001g0169 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.714+15760T>A | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 7/11 | chr17 | 59789645 | |||||||
| chr17:59789835 | C | CT | 68 | a0001c0001t0001g0100 a0001c0001t0001g0101 a0001c0001t0001g0102 others(65): Show |
68 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(65): Show |
intron_variant | MODIFIER | c.714+15972dupT | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr17 | 59789835 | ||||||
| chr17:59789835 | C | CTT | 19 | a0001c0001t0001g0103 a0001c0001t0001g0132 a0001c0001t0001g0175 others(16): Show |
19 | HG00642.hp2 HG01978.hp2 HG01981.hp1 others(16): Show |
intron_variant | MODIFIER | c.714+15971_714+1597 others(6): Show |
VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr17 | 59789835 | ||||||
| chr17:59789835 | C | CTTTTT | 14 | a0001c0001t0001g0076 a0001c0001t0001g0077 a0001c0001t0001g0079 others(11): Show |
14 | HG01891.hp2 HG02257.hp1 HG02258.hp2 others(11): Show |
intron_variant | MODIFIER | c.714+15968_714+1597 others(9): Show |
VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr17 | 59789835 | ||||||
| chr17:59789835 | C | CTTTTTT | 7 | a0001c0001t0001g0003 a0001c0001t0001g0078 a0001c0001t0001g0087 others(4): Show |
7 | HG01243.hp1 HG03098.hp1 HG03453.hp2 others(4): Show |
intron_variant | MODIFIER | c.714+15967_714+1597 others(10): Show |
VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr17 | 59789835 | ||||||
| chr17:59789835 | C | CTTTTTTT | 22 | a0001c0001t0001g0091 a0001c0001t0002g0012 a0001c0001t0002g0020 others(19): Show |
22 | HG00639.hp2 HG00741.hp1 HG01069.hp2 others(19): Show |
intron_variant | MODIFIER | c.714+15966_714+1597 others(11): Show |
VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr17 | 59789835 | ||||||
| chr17:59789835 | C | CTTTTTTT others(1): Show |
39 | a0001c0001t0002g0014 a0001c0001t0002g0016 a0001c0001t0002g0019 others(36): Show |
39 | HG00423.hp2 HG00544.hp1 HG00673.hp1 others(36): Show |
intron_variant | MODIFIER | c.714+15965_714+1597 others(12): Show |
VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr17 | 59789835 | ||||||
| chr17:59789835 | C | CTTTTTTT others(2): Show |
16 | a0001c0001t0001g0089 a0001c0001t0002g0015 a0001c0001t0002g0032 others(13): Show |
16 | HG00408.hp2 HG00621.hp1 HG01358.hp1 others(13): Show |
intron_variant | MODIFIER | c.714+15964_714+1597 others(13): Show |
VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr17 | 59789835 | ||||||
| chr17:59789835 | C | CTTTTTTT others(3): Show |
1 | a0001c0001t0002g0017 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.714+15963_714+1597 others(14): Show |
VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr17 | 59789835 | ||||||
| chr17:59789835 | C | CTTTTTTT others(6): Show |
1 | a0001c0001t0001g0095 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.714+15960_714+1597 others(17): Show |
VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr17 | 59789835 | ||||||
| chr17:59789835 | CTT | C | 26 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(23): Show |
26 | HG00642.hp1 HG00738.hp2 HG01099.hp1 others(23): Show |
intron_variant | MODIFIER | c.714+15971_714+1597 others(6): Show |
VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr17 | 59789835 | ||||||
| chr17:59789835 | CTTT | C | 47 | a0001c0001t0001g0277 a0001c0001t0003g0105 a0001c0001t0003g0107 others(44): Show |
47 | HG00438.hp2 HG00673.hp2 HG01069.hp1 others(44): Show |
intron_variant | MODIFIER | c.714+15970_714+1597 others(7): Show |
VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr17 | 59789835 | ||||||
| chr17:59789932 | C | T | 3 | a0001c0001t0001g0076 a0001c0001t0001g0082 a0001c0001t0001g0087 |
3 | HG02559.hp1 HG02717.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.714+16047C>T | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 7/11 | chr17 | 59789932 | |||||||
| chr17:59789949 | C | T | 11 | a0001c0001t0004g0262 a0001c0001t0004g0263 a0001c0001t0004g0265 others(8): Show |
11 | HG01109.hp2 HG02615.hp1 HG02896.hp1 others(8): Show |
intron_variant | MODIFIER | c.714+16064C>T | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 7/11 | chr17 | 59789949 | |||||||
| chr17:59790083 | C | T | 2 | a0001c0001t0001g0088 a0001c0001t0001g0090 |
2 | HG02622.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.714+16198C>T | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 7/11 | chr17 | 59790083 | |||||||
| chr17:59790263 | G | C | 11 | a0001c0001t0004g0262 a0001c0001t0004g0263 a0001c0001t0004g0265 others(8): Show |
11 | HG01109.hp2 HG02615.hp1 HG02896.hp1 others(8): Show |
intron_variant | MODIFIER | c.714+16378G>C | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 7/11 | chr17 | 59790263 | |||||||
| chr17:59790444 | G | A | 1 | a0001c0001t0001g0207 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.714+16559G>A | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 7/11 | chr17 | 59790444 | |||||||
| chr17:59790647 | G | A | 11 | a0001c0001t0004g0262 a0001c0001t0004g0263 a0001c0001t0004g0265 others(8): Show |
11 | HG01109.hp2 HG02615.hp1 HG02896.hp1 others(8): Show |
intron_variant | MODIFIER | c.714+16762G>A | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 7/11 | chr17 | 59790647 | |||||||
| chr17:59791184 | C | CT | 101 | a0001c0001t0001g0003 a0001c0001t0001g0076 a0001c0001t0001g0077 others(98): Show |
101 | HG00408.hp2 HG00423.hp2 HG00544.hp1 others(98): Show |
intron_variant | MODIFIER | c.714+17320dupT | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr17 | 59791184 | ||||||
| chr17:59791184 | C | CTT | 6 | a0001c0001t0001g0080 a0001c0001t0002g0017 a0001c0001t0002g0032 others(3): Show |
6 | HG03209.hp1 NA18949.hp1 NA18967.hp1 others(3): Show |
intron_variant | MODIFIER | c.714+17319_714+1732 others(6): Show |
VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr17 | 59791184 | ||||||
| chr17:59791184 | CTTTTTTT | C | 85 | a0001c0001t0001g0100 a0001c0001t0001g0101 a0001c0001t0001g0102 others(82): Show |
85 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(82): Show |
intron_variant | MODIFIER | c.714+17314_714+1732 others(11): Show |
VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr17 | 59791184 | ||||||
| chr17:59791240 | G | A | 103 | a0001c0001t0001g0003 a0001c0001t0001g0076 a0001c0001t0001g0077 others(100): Show |
103 | HG00408.hp2 HG00423.hp2 HG00544.hp1 others(100): Show |
intron_variant | MODIFIER | c.714+17355G>A | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 7/11 | chr17 | 59791240 | |||||||
| chr17:59791481 | G | A | 2 | a0001c0001t0001g0153 a0001c0001t0001g0170 |
2 | HG03041.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.715-17315G>A | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 7/11 | chr17 | 59791481 | |||||||
| chr17:59791491 | C | CT | 18 | a0001c0001t0001g0008 a0001c0001t0001g0103 a0001c0001t0001g0150 others(15): Show |
18 | HG00423.hp1 HG00621.hp2 HG00673.hp2 others(15): Show |
intron_variant | MODIFIER | c.715-17287dupT | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr17 | 59791491 | ||||||
| chr17:59791491 | CT | C | 12 | a0001c0001t0002g0062 a0001c0001t0004g0262 a0001c0001t0004g0263 others(9): Show |
12 | HG01109.hp2 HG02615.hp1 HG02896.hp1 others(9): Show |
intron_variant | MODIFIER | c.715-17287delT | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr17 | 59791491 | ||||||
| chr17:59791812 | G | A | 2 | a0001c0001t0003g0113 a0001c0001t0009g0109 |
2 | HG00642.hp1 HG03831.hp2 |
intron_variant | MODIFIER | c.715-16984G>A | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 7/11 | chr17 | 59791812 | |||||||
| chr17:59792042 | T | A | 8 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(5): Show |
8 | HG01099.hp1 HG01884.hp1 HG01952.hp2 others(5): Show |
intron_variant | MODIFIER | c.715-16754T>A | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 7/11 | chr17 | 59792042 | |||||||
| chr17:59792303 | C | T | 8 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(5): Show |
8 | HG01099.hp1 HG01884.hp1 HG01952.hp2 others(5): Show |
intron_variant | MODIFIER | c.715-16493C>T | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 7/11 | chr17 | 59792303 | |||||||
| chr17:59792414 | A | G | 1 | a0001c0001t0003g0149 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.715-16382A>G | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 7/11 | chr17 | 59792414 | |||||||
| chr17:59792455 | T | A | 2 | a0001c0001t0001g0225 a0001c0001t0001g0241 |
2 | HG01978.hp2 HG02145.hp1 |
intron_variant | MODIFIER | c.715-16341T>A | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 7/11 | chr17 | 59792455 | |||||||
| chr17:59792603 | G | A | 2 | a0001c0001t0001g0088 a0001c0001t0001g0090 |
2 | HG02622.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.715-16193G>A | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 7/11 | chr17 | 59792603 | |||||||
| chr17:59792619 | C | T | 1 | a0001c0001t0001g0208 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.715-16177C>T | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 7/11 | chr17 | 59792619 | |||||||
| chr17:59792854 | A | AAAT | 35 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0007 others(32): Show |
35 | HG00738.hp2 HG01069.hp1 HG01099.hp1 others(32): Show |
intron_variant | MODIFIER | c.715-15920_715-1591 others(7): Show |
VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr17 | 59792854 | ||||||
| chr17:59792854 | A | AAATAAT | 4 | a0001c0001t0003g0146 a0001c0001t0004g0269 a0001c0001t0004g0270 others(1): Show |
4 | HG02615.hp1 HG02895.hp1 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.715-15923_715-1591 others(10): Show |
VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr17 | 59792854 | ||||||
| chr17:59792854 | A | AAATAATA others(2): Show |
15 | a0001c0001t0001g0277 a0001c0001t0003g0110 a0001c0001t0003g0112 others(12): Show |
15 | HG00673.hp2 HG02027.hp2 HG02630.hp2 others(12): Show |
intron_variant | MODIFIER | c.715-15926_715-1591 others(13): Show |
VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr17 | 59792854 | ||||||
| chr17:59792854 | A | AAATAATA others(5): Show |
15 | a0001c0001t0003g0107 a0001c0001t0003g0108 a0001c0001t0003g0111 others(12): Show |
15 | HG00438.hp2 HG01071.hp1 HG01168.hp2 others(12): Show |
intron_variant | MODIFIER | c.715-15929_715-1591 others(16): Show |
VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr17 | 59792854 | ||||||
| chr17:59792854 | A | AAATAATA others(8): Show |
9 | a0001c0001t0003g0105 a0001c0001t0003g0113 a0001c0001t0003g0134 others(6): Show |
9 | HG00642.hp1 HG02647.hp1 HG02717.hp1 others(6): Show |
intron_variant | MODIFIER | c.715-15932_715-1591 others(19): Show |
VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr17 | 59792854 | ||||||
| chr17:59792854 | A | AAATAATA others(11): Show |
1 | a0001c0001t0003g0141 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.715-15935_715-1591 others(22): Show |
VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr17 | 59792854 | ||||||
| chr17:59792854 | AAATAATA others(962): Show |
A | 87 | a0001c0001t0001g0100 a0001c0001t0001g0101 a0001c0001t0001g0102 others(84): Show |
87 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(84): Show |
intron_variant | MODIFIER | c.715-15940_715-1497 others(4): Show |
VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr17 | 59792854 | ||||||
| chr17:59792876 | A | T | 5 | a0001c0001t0001g0153 a0001c0001t0001g0165 a0001c0001t0001g0170 others(2): Show |
5 | HG01891.hp1 HG02559.hp2 HG03041.hp1 others(2): Show |
intron_variant | MODIFIER | c.715-15920A>T | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 7/11 | chr17 | 59792876 | |||||||
| chr17:59792876 | AATTATT | A | 22 | a0001c0001t0001g0003 a0001c0001t0001g0076 a0001c0001t0001g0077 others(19): Show |
22 | HG01243.hp1 HG01891.hp2 HG02257.hp1 others(19): Show |
intron_variant | MODIFIER | c.715-15908_715-1590 others(10): Show |
VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr17 | 59792876 | ||||||
| chr17:59792879 | T | A | 153 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(150): Show |
153 | HG00408.hp2 HG00423.hp2 HG00438.hp2 others(150): Show |
intron_variant | MODIFIER | c.715-15917T>A | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 7/11 | chr17 | 59792879 | |||||||
| chr17:59792882 | T | A | 155 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(152): Show |
155 | HG00408.hp2 HG00423.hp2 HG00438.hp2 others(152): Show |
intron_variant | MODIFIER | c.715-15914T>A | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 7/11 | chr17 | 59792882 | |||||||
| chr17:59792885 | T | A | 177 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(174): Show |
177 | HG00408.hp2 HG00423.hp2 HG00438.hp2 others(174): Show |
intron_variant | MODIFIER | c.715-15911T>A | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 7/11 | chr17 | 59792885 | |||||||
| chr17:59792888 | T | A | 177 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(174): Show |
177 | HG00408.hp2 HG00423.hp2 HG00438.hp2 others(174): Show |
intron_variant | MODIFIER | c.715-15908T>A | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 7/11 | chr17 | 59792888 | |||||||
| chr17:59792891 | T | A | 1 | a0001c0001t0001g0005 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.715-15905T>A | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 7/11 | chr17 | 59792891 | |||||||
| chr17:59793419 | G | C | 177 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(174): Show |
177 | HG00408.hp2 HG00423.hp2 HG00438.hp2 others(174): Show |
intron_variant | MODIFIER | c.715-15377G>C | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 7/11 | chr17 | 59793419 | |||||||
| chr17:59793605 | C | T | 1 | a0001c0001t0001g0170 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.715-15191C>T | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 7/11 | chr17 | 59793605 | |||||||
| chr17:59793645 | G | T | 4 | a0001c0001t0001g0078 a0001c0001t0001g0079 a0001c0001t0001g0080 others(1): Show |
4 | HG01243.hp1 HG02451.hp2 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.715-15151G>T | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 7/11 | chr17 | 59793645 | |||||||
| chr17:59793761 | A | G | 177 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(174): Show |
177 | HG00408.hp2 HG00423.hp2 HG00438.hp2 others(174): Show |
intron_variant | MODIFIER | c.715-15035A>G | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 7/11 | chr17 | 59793761 | |||||||
| chr17:59793859 | T | G | 1 | a0001c0001t0001g0160 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.715-14937T>G | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 7/11 | chr17 | 59793859 | |||||||
| chr17:59794018 | T | C | 11 | a0001c0001t0004g0262 a0001c0001t0004g0263 a0001c0001t0004g0265 others(8): Show |
11 | HG01109.hp2 HG02615.hp1 HG02896.hp1 others(8): Show |
intron_variant | MODIFIER | c.715-14778T>C | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 7/11 | chr17 | 59794018 | |||||||
| chr17:59794077 | C | T | 2 | a0001c0001t0003g0131 a0001c0001t0011g0021 |
2 | NA19085.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.715-14719C>T | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 7/11 | chr17 | 59794077 | |||||||
| chr17:59794219 | C | CT | 39 | a0001c0001t0001g0166 a0001c0001t0001g0173 a0001c0001t0002g0062 others(36): Show |
39 | HG00642.hp1 HG00673.hp2 HG00738.hp2 others(36): Show |
intron_variant | MODIFIER | c.715-14556dupT | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr17 | 59794219 | ||||||
| chr17:59794219 | C | CTT | 17 | a0001c0001t0003g0120 a0001c0001t0003g0124 a0001c0001t0003g0130 others(14): Show |
17 | HG01109.hp2 HG01934.hp2 HG02027.hp2 others(14): Show |
intron_variant | MODIFIER | c.715-14557_715-1455 others(6): Show |
VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr17 | 59794219 | ||||||
| chr17:59794219 | CT | C | 118 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(115): Show |
118 | HG00408.hp2 HG00423.hp2 HG00544.hp1 others(115): Show |
intron_variant | MODIFIER | c.715-14556delT | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr17 | 59794219 | ||||||
| chr17:59794219 | CTT | C | 70 | a0001c0001t0001g0100 a0001c0001t0001g0101 a0001c0001t0001g0102 others(67): Show |
70 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(67): Show |
intron_variant | MODIFIER | c.715-14557_715-1455 others(6): Show |
VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr17 | 59794219 | ||||||
| chr17:59794368 | C | T | 1 | a0001c0001t0001g0277 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.715-14428C>T | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 7/11 | chr17 | 59794368 | |||||||
| chr17:59794376 | C | T | 54 | a0001c0001t0001g0277 a0001c0001t0003g0105 a0001c0001t0003g0107 others(51): Show |
54 | HG00438.hp2 HG00642.hp1 HG00673.hp2 others(51): Show |
intron_variant | MODIFIER | c.715-14420C>T | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 7/11 | chr17 | 59794376 | |||||||
| chr17:59794425 | G | C | 3 | a0001c0001t0001g0206 a0001c0001t0001g0209 a0001c0001t0001g0224 |
3 | HG00621.hp2 HG02040.hp1 HG02129.hp2 |
intron_variant | MODIFIER | c.715-14371G>C | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 7/11 | chr17 | 59794425 | |||||||
| chr17:59794507 | C | T | 1 | a0001c0001t0003g0110 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.715-14289C>T | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 7/11 | chr17 | 59794507 | |||||||
| chr17:59794509 | C | T | 1 | a0002c0003t0002g0030 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.715-14287C>T | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 7/11 | chr17 | 59794509 | |||||||
| chr17:59794517 | AT | A | 13 | a0001c0001t0001g0069 a0001c0001t0001g0150 a0001c0001t0001g0153 others(10): Show |
13 | HG00140.hp1 HG01255.hp1 HG01256.hp1 others(10): Show |
intron_variant | MODIFIER | c.715-14245delT | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr17 | 59794517 | ||||||
| chr17:59794517 | ATTT | A | 25 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0007 others(22): Show |
25 | HG00673.hp2 HG00741.hp1 HG01099.hp1 others(22): Show |
intron_variant | MODIFIER | c.715-14247_715-1424 others(7): Show |
VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr17 | 59794517 | ||||||
| chr17:59794517 | ATTTT | A | 55 | a0001c0001t0001g0089 a0001c0001t0002g0013 a0001c0001t0002g0014 others(52): Show |
55 | HG00438.hp2 HG00639.hp2 HG00642.hp1 others(52): Show |
intron_variant | MODIFIER | c.715-14248_715-1424 others(8): Show |
VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr17 | 59794517 | ||||||
| chr17:59794517 | ATTTTT | A | 68 | a0001c0001t0001g0083 a0001c0001t0001g0088 a0001c0001t0001g0092 others(65): Show |
68 | HG00408.hp2 HG00423.hp2 HG00544.hp1 others(65): Show |
intron_variant | MODIFIER | c.715-14249_715-1424 others(9): Show |
VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr17 | 59794517 | ||||||
| chr17:59794517 | ATTTTTT | A | 48 | a0001c0001t0001g0003 a0001c0001t0001g0076 a0001c0001t0001g0077 others(45): Show |
48 | HG00621.hp2 HG00741.hp2 HG01243.hp1 others(45): Show |
intron_variant | MODIFIER | c.715-14250_715-1424 others(10): Show |
VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr17 | 59794517 | ||||||
| chr17:59794517 | ATTTTTTT | A | 59 | a0001c0001t0001g0100 a0001c0001t0001g0101 a0001c0001t0001g0102 others(56): Show |
59 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(56): Show |
intron_variant | MODIFIER | c.715-14251_715-1424 others(11): Show |
VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr17 | 59794517 | ||||||
| chr17:59794517 | ATTTTTTT others(1): Show |
A | 7 | a0001c0001t0001g0139 a0001c0001t0001g0175 a0001c0001t0001g0220 others(4): Show |
7 | HG00642.hp2 HG01256.hp2 HG01981.hp1 others(4): Show |
intron_variant | MODIFIER | c.715-14252_715-1424 others(12): Show |
VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr17 | 59794517 | ||||||
| chr17:59794551 | T | A | 4 | a0001c0001t0001g0100 a0001c0001t0001g0101 a0001c0001t0001g0102 others(1): Show |
4 | HG01261.hp2 HG01358.hp2 HG02738.hp2 others(1): Show |
intron_variant | MODIFIER | c.715-14245T>A | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 7/11 | chr17 | 59794551 | |||||||
| chr17:59794597 | A | G | 1 | a0001c0001t0003g0105 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.715-14199A>G | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 7/11 | chr17 | 59794597 | |||||||
| chr17:59794726 | T | A | 3 | a0001c0001t0002g0049 a0001c0001t0002g0096 a0001c0001t0002g0097 |
3 | HG00544.hp1 HG02683.hp2 NA18982.hp1 |
intron_variant | MODIFIER | c.715-14070T>A | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 7/11 | chr17 | 59794726 | |||||||
| chr17:59794879 | C | T | 5 | a0001c0001t0003g0151 a0001c0001t0003g0258 a0001c0001t0003g0259 others(2): Show |
5 | HG02896.hp2 HG03195.hp1 HG03471.hp2 others(2): Show |
intron_variant | MODIFIER | c.715-13917C>T | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 7/11 | chr17 | 59794879 | |||||||
| chr17:59794927 | C | T | 3 | a0001c0001t0001g0204 a0001c0001t0001g0238 a0001c0001t0014g0189 |
3 | HG02922.hp2 HG02965.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.715-13869C>T | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 7/11 | chr17 | 59794927 | |||||||
| chr17:59794995 | C | CT | 154 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0006 others(151): Show |
154 | HG00408.hp2 HG00423.hp2 HG00438.hp2 others(151): Show |
intron_variant | MODIFIER | c.715-13782dupT | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr17 | 59794995 | ||||||
| chr17:59794995 | C | CTT | 27 | a0001c0001t0001g0005 a0001c0001t0001g0081 a0001c0001t0001g0084 others(24): Show |
27 | HG00642.hp1 HG01258.hp1 HG01884.hp2 others(24): Show |
intron_variant | MODIFIER | c.715-13783_715-1378 others(6): Show |
VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr17 | 59794995 | ||||||
| chr17:59794995 | C | CTTT | 71 | a0001c0001t0001g0092 a0001c0001t0001g0100 a0001c0001t0001g0101 others(68): Show |
71 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(68): Show |
intron_variant | MODIFIER | c.715-13784_715-1378 others(7): Show |
VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr17 | 59794995 | ||||||
| chr17:59794995 | C | CTTTT | 7 | a0001c0001t0001g0103 a0001c0001t0001g0186 a0001c0001t0001g0187 others(4): Show |
7 | HG00741.hp2 HG02071.hp1 HG02723.hp2 others(4): Show |
intron_variant | MODIFIER | c.715-13785_715-1378 others(8): Show |
VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr17 | 59794995 | ||||||
| chr17:59795133 | G | A | 104 | a0001c0001t0001g0003 a0001c0001t0001g0076 a0001c0001t0001g0077 others(101): Show |
104 | HG00408.hp2 HG00423.hp2 HG00544.hp1 others(101): Show |
intron_variant | MODIFIER | c.715-13663G>A | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 7/11 | chr17 | 59795133 | |||||||
| chr17:59795146 | C | T | 11 | a0001c0001t0004g0262 a0001c0001t0004g0263 a0001c0001t0004g0265 others(8): Show |
11 | HG01109.hp2 HG02615.hp1 HG02896.hp1 others(8): Show |
intron_variant | MODIFIER | c.715-13650C>T | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 7/11 | chr17 | 59795146 | |||||||
| chr17:59795408 | T | C | 3 | a0001c0001t0002g0049 a0001c0001t0002g0096 a0001c0001t0002g0097 |
3 | HG00544.hp1 HG02683.hp2 NA18982.hp1 |
intron_variant | MODIFIER | c.715-13388T>C | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 7/11 | chr17 | 59795408 | |||||||
| chr17:59795412 | T | C | 1 | a0001c0001t0001g0095 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.715-13384T>C | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 7/11 | chr17 | 59795412 | |||||||
| chr17:59795477 | C | G | 1 | a0001c0001t0003g0142 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.715-13319C>G | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 7/11 | chr17 | 59795477 | |||||||
| chr17:59795479 | T | A | 1 | a0001c0001t0003g0142 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.715-13317T>A | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 7/11 | chr17 | 59795479 | |||||||
| chr17:59795481 | C | A | 1 | a0001c0001t0003g0142 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.715-13315C>A | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 7/11 | chr17 | 59795481 | |||||||
| chr17:59795484 | C | A | 1 | a0001c0001t0003g0142 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.715-13312C>A | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 7/11 | chr17 | 59795484 | |||||||
| chr17:59795485 | T | A | 1 | a0001c0001t0003g0142 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.715-13311T>A | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 7/11 | chr17 | 59795485 | |||||||
| chr17:59795486 | T | G | 1 | a0001c0001t0003g0142 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.715-13310T>G | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 7/11 | chr17 | 59795486 | |||||||
| chr17:59795487 | T | G | 1 | a0001c0001t0003g0142 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.715-13309T>G | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 7/11 | chr17 | 59795487 | |||||||
| chr17:59795490 | T | G | 1 | a0001c0001t0003g0142 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.715-13306T>G | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 7/11 | chr17 | 59795490 | |||||||
| chr17:59795492 | T | G | 1 | a0001c0001t0003g0142 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.715-13304T>G | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 7/11 | chr17 | 59795492 | |||||||
| chr17:59795493 | G | A | 1 | a0001c0001t0003g0142 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.715-13303G>A | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 7/11 | chr17 | 59795493 | |||||||
| chr17:59795496 | C | G | 1 | a0001c0001t0003g0142 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.715-13300C>G | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 7/11 | chr17 | 59795496 | |||||||
| chr17:59795498 | T | A | 1 | a0001c0001t0003g0142 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.715-13298T>A | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 7/11 | chr17 | 59795498 | |||||||
| chr17:59795500 | T | G | 1 | a0001c0001t0003g0142 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.715-13296T>G | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 7/11 | chr17 | 59795500 | |||||||
| chr17:59795501 | T | A | 1 | a0001c0001t0003g0142 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.715-13295T>A | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 7/11 | chr17 | 59795501 | |||||||
| chr17:59795502 | T | A | 1 | a0001c0001t0003g0142 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.715-13294T>A | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 7/11 | chr17 | 59795502 | |||||||
| chr17:59795503 | C | A | 1 | a0001c0001t0003g0142 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.715-13293C>A | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 7/11 | chr17 | 59795503 | |||||||
| chr17:59795504 | T | A | 1 | a0001c0001t0003g0142 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.715-13292T>A | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 7/11 | chr17 | 59795504 | |||||||
| chr17:59795506 | T | A | 1 | a0001c0001t0003g0142 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.715-13290T>A | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 7/11 | chr17 | 59795506 | |||||||
| chr17:59795508 | G | A | 1 | a0001c0001t0003g0142 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.715-13288G>A | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 7/11 | chr17 | 59795508 | |||||||
| chr17:59795510 | T | C | 1 | a0001c0001t0003g0142 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.715-13286T>C | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 7/11 | chr17 | 59795510 | |||||||
| chr17:59795512 | T | A | 1 | a0001c0001t0003g0142 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.715-13284T>A | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 7/11 | chr17 | 59795512 | |||||||
| chr17:59795513 | T | A | 1 | a0001c0001t0003g0142 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.715-13283T>A | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 7/11 | chr17 | 59795513 | |||||||
| chr17:59795514 | T | A | 1 | a0001c0001t0003g0142 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.715-13282T>A | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 7/11 | chr17 | 59795514 | |||||||
| chr17:59795517 | A | T | 1 | a0001c0001t0003g0142 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.715-13279A>T | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 7/11 | chr17 | 59795517 | |||||||
| chr17:59795518 | A | C | 1 | a0001c0001t0003g0142 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.715-13278A>C | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 7/11 | chr17 | 59795518 | |||||||
| chr17:59795520 | T | A | 1 | a0001c0001t0003g0142 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.715-13276T>A | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 7/11 | chr17 | 59795520 | |||||||
| chr17:59795526 | C | T | 1 | a0001c0001t0003g0142 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.715-13270C>T | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 7/11 | chr17 | 59795526 | |||||||
| chr17:59795527 | A | T | 1 | a0001c0001t0003g0142 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.715-13269A>T | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 7/11 | chr17 | 59795527 | |||||||
| chr17:59795532 | T | C | 1 | a0001c0001t0003g0142 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.715-13264T>C | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 7/11 | chr17 | 59795532 | |||||||
| chr17:59795534 | G | A | 1 | a0001c0001t0003g0142 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.715-13262G>A | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 7/11 | chr17 | 59795534 | |||||||
| chr17:59795545 | C | T | 1 | a0001c0001t0003g0142 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.715-13251C>T | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 7/11 | chr17 | 59795545 | |||||||
| chr17:59795713 | C | T | 1 | a0001c0001t0001g0201 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.715-13083C>T | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 7/11 | chr17 | 59795713 | |||||||
| chr17:59796301 | C | T | 2 | a0001c0001t0001g0181 a0001c0001t0001g0219 |
2 | HG02083.hp1 NA18973.hp1 |
intron_variant | MODIFIER | c.715-12495C>T | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 7/11 | chr17 | 59796301 | |||||||
| chr17:59796355 | G | A | 1 | a0001c0001t0001g0088 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.715-12441G>A | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 7/11 | chr17 | 59796355 | |||||||
| chr17:59796652 | T | C | 2 | a0001c0001t0001g0180 a0001c0001t0001g0214 |
2 | NA19057.hp1 NA19077.hp2 |
intron_variant | MODIFIER | c.715-12144T>C | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 7/11 | chr17 | 59796652 | |||||||
| chr17:59796956 | A | T | 1 | a0001c0001t0002g0028 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.715-11840A>T | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 7/11 | chr17 | 59796956 | |||||||
| chr17:59797069 | C | G | 1 | a0001c0001t0002g0024 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.715-11727C>G | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 7/11 | chr17 | 59797069 | |||||||
| chr17:59797156 | AC | A | 120 | a0001c0001t0001g0095 a0001c0001t0001g0277 a0001c0001t0002g0012 others(117): Show |
120 | HG00408.hp2 HG00423.hp2 HG00544.hp1 others(117): Show |
intron_variant | MODIFIER | c.715-11630delC | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr17 | 59797156 | ||||||
| chr17:59797156 | ACC | A | 21 | a0001c0001t0001g0003 a0001c0001t0001g0076 a0001c0001t0001g0077 others(18): Show |
21 | HG01243.hp1 HG01891.hp2 HG02257.hp1 others(18): Show |
intron_variant | MODIFIER | c.715-11631_715-1163 others(6): Show |
VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr17 | 59797156 | ||||||
| chr17:59797650 | G | A | 8 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(5): Show |
8 | HG01099.hp1 HG01884.hp1 HG01952.hp2 others(5): Show |
intron_variant | MODIFIER | c.715-11146G>A | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 7/11 | chr17 | 59797650 | |||||||
| chr17:59797709 | G | A | 4 | a0001c0001t0001g0175 a0001c0001t0001g0220 a0001c0001t0001g0225 others(1): Show |
4 | HG00642.hp2 HG01978.hp2 HG01981.hp1 others(1): Show |
intron_variant | MODIFIER | c.715-11087G>A | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 7/11 | chr17 | 59797709 | |||||||
| chr17:59797833 | C | T | 1 | a0001c0001t0003g0257 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.715-10963C>T | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 7/11 | chr17 | 59797833 | |||||||
| chr17:59797838 | C | T | 1 | a0001c0001t0002g0064 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.715-10958C>T | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 7/11 | chr17 | 59797838 | |||||||
| chr17:59797913 | A | G | 1 | a0001c0001t0001g0208 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.715-10883A>G | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 7/11 | chr17 | 59797913 | |||||||
| chr17:59797931 | G | A | 76 | a0001c0001t0001g0100 a0001c0001t0001g0101 a0001c0001t0001g0102 others(73): Show |
76 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(73): Show |
intron_variant | MODIFIER | c.715-10865G>A | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 7/11 | chr17 | 59797931 | |||||||
| chr17:59797940 | A | G | 11 | a0001c0001t0004g0262 a0001c0001t0004g0263 a0001c0001t0004g0265 others(8): Show |
11 | HG01109.hp2 HG02615.hp1 HG02896.hp1 others(8): Show |
intron_variant | MODIFIER | c.715-10856A>G | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 7/11 | chr17 | 59797940 | |||||||
| chr17:59798035 | C | T | 87 | a0001c0001t0001g0100 a0001c0001t0001g0101 a0001c0001t0001g0102 others(84): Show |
87 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(84): Show |
intron_variant | MODIFIER | c.715-10761C>T | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 7/11 | chr17 | 59798035 | |||||||
| chr17:59798078 | T | C | 1 | a0001c0001t0002g0041 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.715-10718T>C | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 7/11 | chr17 | 59798078 | |||||||
| chr17:59798193 | G | A | 78 | a0001c0001t0002g0012 a0001c0001t0002g0013 a0001c0001t0002g0014 others(75): Show |
78 | HG00408.hp2 HG00423.hp2 HG00544.hp1 others(75): Show |
intron_variant | MODIFIER | c.715-10603G>A | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 7/11 | chr17 | 59798193 | |||||||
| chr17:59798546 | A | G | 103 | a0001c0001t0001g0003 a0001c0001t0001g0076 a0001c0001t0001g0077 others(100): Show |
103 | HG00408.hp2 HG00423.hp2 HG00544.hp1 others(100): Show |
intron_variant | MODIFIER | c.715-10250A>G | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 7/11 | chr17 | 59798546 | |||||||
| chr17:59798594 | A | G | 2 | a0001c0001t0003g0136 a0001c0001t0003g0147 |
2 | HG00438.hp2 NA18992.hp2 |
intron_variant | MODIFIER | c.715-10202A>G | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 7/11 | chr17 | 59798594 | |||||||
| chr17:59798608 | C | A | 1 | a0001c0001t0002g0042 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.715-10188C>A | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 7/11 | chr17 | 59798608 | |||||||
| chr17:59798747 | G | A | 4 | a0001c0001t0006g0283 a0001c0001t0006g0284 a0001c0001t0006g0285 others(1): Show |
4 | HG02109.hp2 HG03130.hp2 HG06807.hp2 others(1): Show |
intron_variant | MODIFIER | c.715-10049G>A | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 7/11 | chr17 | 59798747 | |||||||
| chr17:59798846 | A | T | 8 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(5): Show |
8 | HG01099.hp1 HG01884.hp1 HG01952.hp2 others(5): Show |
intron_variant | MODIFIER | c.715-9950A>T | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 7/11 | chr17 | 59798846 | |||||||
| chr17:59798905 | G | T | 1 | a0001c0001t0002g0060 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.715-9891G>T | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 7/11 | chr17 | 59798905 | |||||||
| chr17:59799114 | G | C | 1 | a0001c0001t0003g0122 | 1 | NA19080.hp2 | intron_variant | MODIFIER | c.715-9682G>C | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 7/11 | chr17 | 59799114 | |||||||
| chr17:59799688 | C | T | 103 | a0001c0001t0001g0003 a0001c0001t0001g0076 a0001c0001t0001g0077 others(100): Show |
103 | HG00408.hp2 HG00423.hp2 HG00544.hp1 others(100): Show |
intron_variant | MODIFIER | c.715-9108C>T | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 7/11 | chr17 | 59799688 | |||||||
| chr17:59799820 | A | T | 1 | a0001c0001t0001g0175 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.715-8976A>T | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 7/11 | chr17 | 59799820 | |||||||
| chr17:59799843 | G | A | 1 | a0001c0001t0001g0095 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.715-8953G>A | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 7/11 | chr17 | 59799843 | |||||||
| chr17:59799852 | A | G | 11 | a0001c0001t0004g0262 a0001c0001t0004g0263 a0001c0001t0004g0265 others(8): Show |
11 | HG01109.hp2 HG02615.hp1 HG02896.hp1 others(8): Show |
intron_variant | MODIFIER | c.715-8944A>G | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 7/11 | chr17 | 59799852 | |||||||
| chr17:59799855 | C | T | 1 | a0001c0001t0002g0039 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.715-8941C>T | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 7/11 | chr17 | 59799855 | |||||||
| chr17:59799894 | C | T | 11 | a0001c0001t0004g0262 a0001c0001t0004g0263 a0001c0001t0004g0265 others(8): Show |
11 | HG01109.hp2 HG02615.hp1 HG02896.hp1 others(8): Show |
intron_variant | MODIFIER | c.715-8902C>T | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 7/11 | chr17 | 59799894 | |||||||
| chr17:59799895 | G | A | 1 | a0001c0001t0001g0169 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.715-8901G>A | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 7/11 | chr17 | 59799895 | |||||||
| chr17:59799945 | CA | C | 256 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(253): Show |
256 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(253): Show |
intron_variant | MODIFIER | c.715-8834delA | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr17 | 59799945 | ||||||
| chr17:59800045 | A | T | 1 | a0001c0001t0011g0021 | 1 | NA19085.hp2 | intron_variant | MODIFIER | c.715-8751A>T | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 7/11 | chr17 | 59800045 | |||||||
| chr17:59800118 | A | G | 1 | a0001c0001t0005g0018 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.715-8678A>G | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 7/11 | chr17 | 59800118 | |||||||
| chr17:59800243 | A | G | 1 | a0001c0001t0001g0277 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.715-8553A>G | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 7/11 | chr17 | 59800243 | |||||||
| chr17:59800375 | T | G | 4 | a0001c0001t0006g0283 a0001c0001t0006g0284 a0001c0001t0006g0285 others(1): Show |
4 | HG02109.hp2 HG03130.hp2 HG06807.hp2 others(1): Show |
intron_variant | MODIFIER | c.715-8421T>G | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 7/11 | chr17 | 59800375 | |||||||
| chr17:59800418 | G | A | 2 | a0001c0001t0004g0262 a0001c0001t0004g0263 |
2 | HG01109.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.715-8378G>A | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 7/11 | chr17 | 59800418 | |||||||
| chr17:59800700 | A | G | 1 | a0001c0001t0001g0197 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.715-8096A>G | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 7/11 | chr17 | 59800700 | |||||||
| chr17:59800788 | A | G | 53 | a0001c0001t0003g0105 a0001c0001t0003g0107 a0001c0001t0003g0108 others(50): Show |
53 | HG00438.hp2 HG00642.hp1 HG00673.hp2 others(50): Show |
intron_variant | MODIFIER | c.715-8008A>G | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 7/11 | chr17 | 59800788 | |||||||
| chr17:59800807 | C | G | 3 | a0001c0001t0003g0140 a0001c0001t0003g0144 a0001c0001t0003g0145 |
3 | HG02717.hp1 HG02895.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.715-7989C>G | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 7/11 | chr17 | 59800807 | |||||||
| chr17:59801080 | G | GA | 62 | a0001c0001t0001g0095 a0001c0001t0001g0162 a0001c0001t0001g0170 others(59): Show |
62 | HG00408.hp2 HG00621.hp1 HG00639.hp2 others(59): Show |
intron_variant | MODIFIER | c.715-7704dupA | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr17 | 59801080 | ||||||
| chr17:59801080 | G | GAA | 48 | a0001c0001t0001g0132 a0001c0001t0001g0139 a0001c0001t0001g0168 others(45): Show |
48 | HG00140.hp1 HG00280.hp1 HG00423.hp1 others(45): Show |
intron_variant | MODIFIER | c.715-7705_715-7704d others(4): Show |
VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr17 | 59801080 | ||||||
| chr17:59801080 | G | GAAA | 10 | a0001c0001t0001g0104 a0001c0001t0001g0153 a0001c0001t0001g0249 others(7): Show |
10 | HG01361.hp1 HG01361.hp2 HG02145.hp2 others(7): Show |
intron_variant | MODIFIER | c.715-7706_715-7704d others(5): Show |
VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr17 | 59801080 | ||||||
| chr17:59801080 | GAA | G | 17 | a0001c0001t0003g0111 a0001c0001t0003g0116 a0001c0001t0003g0117 others(14): Show |
17 | HG00738.hp2 HG01069.hp1 HG01071.hp1 others(14): Show |
intron_variant | MODIFIER | c.715-7705_715-7704d others(4): Show |
VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr17 | 59801080 | ||||||
| chr17:59801081 | A | G | 1 | a0001c0001t0001g0166 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.715-7715A>G | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 7/11 | chr17 | 59801081 | |||||||
| chr17:59801089 | A | T | 1 | a0001c0001t0003g0105 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.715-7707A>T | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 7/11 | chr17 | 59801089 | |||||||
| chr17:59801091 | A | AAAAT | 13 | a0001c0001t0001g0174 a0001c0001t0001g0177 a0001c0001t0001g0178 others(10): Show |
13 | HG00438.hp1 HG01978.hp2 HG02040.hp1 others(10): Show |
intron_variant | MODIFIER | c.715-7704_715-7703i others(6): Show |
VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr17 | 59801091 | ||||||
| chr17:59801091 | A | AT | 8 | a0001c0001t0001g0198 a0001c0001t0002g0035 a0001c0001t0002g0042 others(5): Show |
8 | NA18952.hp2 NA18956.hp1 NA18956.hp2 others(5): Show |
intron_variant | MODIFIER | c.715-7705_715-7704i others(3): Show |
VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 7/11 | chr17 | 59801091 | |||||||
| chr17:59801091 | A | T | 32 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0007 others(29): Show |
32 | HG00438.hp2 HG00642.hp1 HG00673.hp2 others(29): Show |
intron_variant | MODIFIER | c.715-7705A>T | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 7/11 | chr17 | 59801091 | |||||||
| chr17:59801092 | AT | A | 17 | a0001c0001t0001g0069 a0001c0001t0001g0070 a0001c0001t0001g0089 others(14): Show |
17 | HG01123.hp1 HG01168.hp1 HG01256.hp1 others(14): Show |
intron_variant | MODIFIER | c.715-7703delT | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 7/11 | chr17 | 59801092 | |||||||
| chr17:59801093 | T | A | 103 | a0001c0001t0001g0077 a0001c0001t0001g0078 a0001c0001t0001g0079 others(100): Show |
103 | HG00140.hp2 HG00408.hp2 HG00423.hp1 others(100): Show |
intron_variant | MODIFIER | c.715-7703T>A | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 7/11 | chr17 | 59801093 | |||||||
| chr17:59801095 | T | A | 33 | a0001c0001t0001g0069 a0001c0001t0001g0070 a0001c0001t0001g0078 others(30): Show |
33 | HG01069.hp2 HG01071.hp2 HG01109.hp2 others(30): Show |
intron_variant | MODIFIER | c.715-7701T>A | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 7/11 | chr17 | 59801095 | |||||||
| chr17:59801097 | T | A | 11 | a0001c0001t0004g0262 a0001c0001t0004g0263 a0001c0001t0004g0265 others(8): Show |
11 | HG01109.hp2 HG02615.hp1 HG02896.hp1 others(8): Show |
intron_variant | MODIFIER | c.715-7699T>A | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 7/11 | chr17 | 59801097 | |||||||
| chr17:59801099 | T | A | 9 | a0001c0001t0004g0262 a0001c0001t0004g0263 a0001c0001t0004g0265 others(6): Show |
9 | HG01109.hp2 HG02615.hp1 HG02896.hp1 others(6): Show |
intron_variant | MODIFIER | c.715-7697T>A | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 7/11 | chr17 | 59801099 | |||||||
| chr17:59801106 | A | G | 1 | a0001c0001t0001g0095 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.715-7690A>G | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 7/11 | chr17 | 59801106 | |||||||
| chr17:59801108 | A | G | 1 | a0001c0001t0001g0095 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.715-7688A>G | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 7/11 | chr17 | 59801108 | |||||||
| chr17:59801108 | ATATATGT others(11): Show |
A | 8 | a0001c0001t0001g0081 a0001c0001t0001g0083 a0001c0001t0001g0084 others(5): Show |
8 | HG01891.hp2 HG02257.hp1 HG02280.hp2 others(5): Show |
intron_variant | MODIFIER | c.715-7686_715-7669d others(20): Show |
VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr17 | 59801108 | ||||||
| chr17:59801110 | A | G | 1 | a0001c0001t0001g0095 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.715-7686A>G | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 7/11 | chr17 | 59801110 | |||||||
| chr17:59801110 | ATATGTGT others(5): Show |
A | 7 | a0001c0001t0001g0003 a0001c0001t0001g0077 a0001c0001t0001g0078 others(4): Show |
7 | HG01243.hp1 HG02258.hp2 HG02451.hp2 others(4): Show |
intron_variant | MODIFIER | c.715-7684_715-7673d others(14): Show |
VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr17 | 59801110 | ||||||
| chr17:59801110 | ATATGTGT others(9): Show |
A | 2 | a0001c0001t0001g0082 a0001c0001t0001g0087 |
2 | HG02559.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.715-7684_715-7669d others(18): Show |
VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr17 | 59801110 | ||||||
| chr17:59801112 | A | ATATATGT others(1): Show |
3 | a0001c0001t0001g0006 a0001c0001t0001g0010 a0001c0001t0001g0233 |
3 | HG02886.hp2 HG03516.hp1 NA18942.hp2 |
intron_variant | MODIFIER | c.715-7683_715-7682i others(10): Show |
VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr17 | 59801112 | ||||||
| chr17:59801112 | A | ATATGTG | 6 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0007 others(3): Show |
6 | HG01099.hp1 HG01884.hp1 HG01952.hp2 others(3): Show |
intron_variant | MODIFIER | c.715-7683_715-7682i others(8): Show |
VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr17 | 59801112 | ||||||
| chr17:59801112 | A | G | 8 | a0001c0001t0001g0095 a0001c0001t0001g0168 a0001c0001t0001g0184 others(5): Show |
8 | HG00140.hp1 HG02145.hp1 HG02723.hp1 others(5): Show |
intron_variant | MODIFIER | c.715-7684A>G | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 7/11 | chr17 | 59801112 | |||||||
| chr17:59801112 | ATG | A | 5 | a0001c0001t0001g0088 a0001c0001t0001g0090 a0001c0001t0002g0050 others(2): Show |
5 | HG02109.hp1 HG02622.hp1 HG03453.hp2 others(2): Show |
intron_variant | MODIFIER | c.715-7648_715-7647d others(4): Show |
VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr17 | 59801112 | ||||||
| chr17:59801112 | ATGTGTG | A | 10 | a0001c0001t0004g0262 a0001c0001t0004g0265 a0001c0001t0004g0266 others(7): Show |
10 | HG01109.hp2 HG02615.hp1 HG02896.hp1 others(7): Show |
intron_variant | MODIFIER | c.715-7652_715-7647d others(8): Show |
VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr17 | 59801112 | ||||||
| chr17:59801112 | ATGTGTGT others(3): Show |
A | 1 | a0001c0001t0001g0089 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.715-7656_715-7647d others(12): Show |
VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr17 | 59801112 | ||||||
| chr17:59801112 | ATGTGTGT others(7): Show |
A | 1 | a0001c0001t0001g0076 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.715-7660_715-7647d others(16): Show |
VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr17 | 59801112 | ||||||
| chr17:59801112 | ATGTGTGT others(9): Show |
A | 1 | a0001c0001t0003g0147 | 1 | NA18992.hp2 | intron_variant | MODIFIER | c.715-7662_715-7647d others(18): Show |
VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr17 | 59801112 | ||||||
| chr17:59801114 | G | A | 163 | a0001c0001t0001g0069 a0001c0001t0001g0070 a0001c0001t0001g0100 others(160): Show |
163 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(160): Show |
intron_variant | MODIFIER | c.715-7682G>A | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 7/11 | chr17 | 59801114 | |||||||
| chr17:59801116 | G | A | 3 | a0001c0001t0001g0202 a0001c0001t0002g0020 a0001c0001t0013g0216 |
3 | HG01168.hp1 HG02109.hp1 HG03654.hp2 |
intron_variant | MODIFIER | c.715-7680G>A | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 7/11 | chr17 | 59801116 | |||||||
| chr17:59801118 | G | A | 1 | a0001c0001t0013g0216 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.715-7678G>A | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 7/11 | chr17 | 59801118 | |||||||
| chr17:59801141 | T | C | 1 | a0001c0001t0001g0204 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.715-7655T>C | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 7/11 | chr17 | 59801141 | |||||||
| chr17:59801146 | G | A | 1 | a0001c0001t0001g0089 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.715-7650G>A | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 7/11 | chr17 | 59801146 | |||||||
| chr17:59801148 | G | A | 140 | a0001c0001t0001g0003 a0001c0001t0001g0076 a0001c0001t0001g0077 others(137): Show |
140 | HG00408.hp2 HG00423.hp2 HG00544.hp1 others(137): Show |
intron_variant | MODIFIER | c.715-7648G>A | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 7/11 | chr17 | 59801148 | |||||||
| chr17:59801148 | G | GTA | 11 | a0001c0001t0001g0277 a0001c0001t0003g0108 a0001c0001t0003g0110 others(8): Show |
11 | HG00438.hp2 HG00673.hp2 HG02071.hp2 others(8): Show |
intron_variant | MODIFIER | c.715-7646_715-7645d others(4): Show |
VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr17 | 59801148 | ||||||
| chr17:59801355 | C | T | 25 | a0001c0001t0001g0003 a0001c0001t0001g0076 a0001c0001t0001g0077 others(22): Show |
25 | HG01243.hp1 HG01891.hp2 HG02109.hp2 others(22): Show |
intron_variant | MODIFIER | c.715-7441C>T | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 7/11 | chr17 | 59801355 | |||||||
| chr17:59801367 | T | G | 1 | a0001c0001t0002g0060 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.715-7429T>G | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 7/11 | chr17 | 59801367 | |||||||
| chr17:59801415 | G | GT | 77 | a0001c0001t0002g0012 a0001c0001t0002g0013 a0001c0001t0002g0014 others(74): Show |
77 | HG00408.hp2 HG00423.hp2 HG00544.hp1 others(74): Show |
intron_variant | MODIFIER | c.715-7370dupT | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr17 | 59801415 | ||||||
| chr17:59801544 | G | A | 8 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(5): Show |
8 | HG01099.hp1 HG01884.hp1 HG01952.hp2 others(5): Show |
intron_variant | MODIFIER | c.715-7252G>A | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 7/11 | chr17 | 59801544 | |||||||
| chr17:59801669 | C | T | 18 | a0001c0001t0001g0003 a0001c0001t0001g0076 a0001c0001t0001g0077 others(15): Show |
18 | HG01243.hp1 HG01891.hp2 HG02257.hp1 others(15): Show |
intron_variant | MODIFIER | c.715-7127C>T | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 7/11 | chr17 | 59801669 | |||||||
| chr17:59801938 | C | T | 1 | a0001c0001t0001g0095 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.715-6858C>T | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 7/11 | chr17 | 59801938 | |||||||
| chr17:59802022 | G | A | 1 | a0001c0001t0001g0242 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.715-6774G>A | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 7/11 | chr17 | 59802022 | |||||||
| chr17:59802249 | A | G | 87 | a0001c0001t0001g0100 a0001c0001t0001g0101 a0001c0001t0001g0102 others(84): Show |
87 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(84): Show |
intron_variant | MODIFIER | c.715-6547A>G | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 7/11 | chr17 | 59802249 | |||||||
| chr17:59802840 | G | A | 103 | a0001c0001t0001g0003 a0001c0001t0001g0076 a0001c0001t0001g0077 others(100): Show |
103 | HG00408.hp2 HG00423.hp2 HG00544.hp1 others(100): Show |
intron_variant | MODIFIER | c.715-5956G>A | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 7/11 | chr17 | 59802840 | |||||||
| chr17:59802913 | AT | A | 87 | a0001c0001t0001g0100 a0001c0001t0001g0101 a0001c0001t0001g0102 others(84): Show |
87 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(84): Show |
intron_variant | MODIFIER | c.715-5879delT | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr17 | 59802913 | ||||||
| chr17:59802974 | G | A | 1 | a0001c0001t0002g0063 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.715-5822G>A | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 7/11 | chr17 | 59802974 | |||||||
| chr17:59803064 | A | G | 1 | a0001c0001t0003g0125 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.715-5732A>G | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 7/11 | chr17 | 59803064 | |||||||
| chr17:59803510 | T | C | 1 | a0001c0001t0003g0257 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.715-5286T>C | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 7/11 | chr17 | 59803510 | |||||||
| chr17:59803949 | A | AT | 87 | a0001c0001t0001g0100 a0001c0001t0001g0101 a0001c0001t0001g0102 others(84): Show |
87 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(84): Show |
intron_variant | MODIFIER | c.715-4839dupT | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr17 | 59803949 | ||||||
| chr17:59803983 | T | A | 1 | a0001c0001t0001g0166 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.715-4813T>A | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 7/11 | chr17 | 59803983 | |||||||
| chr17:59803983 | T | G | 1 | a0001c0001t0003g0257 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.715-4813T>G | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 7/11 | chr17 | 59803983 | |||||||
| chr17:59804339 | C | T | 2 | a0001c0001t0001g0180 a0001c0001t0001g0214 |
2 | NA19057.hp1 NA19077.hp2 |
intron_variant | MODIFIER | c.715-4457C>T | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 7/11 | chr17 | 59804339 | |||||||
| chr17:59804443 | A | G | 1 | a0001c0001t0001g0095 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.715-4353A>G | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 7/11 | chr17 | 59804443 | |||||||
| chr17:59804476 | G | A | 1 | a0001c0001t0001g0095 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.715-4320G>A | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 7/11 | chr17 | 59804476 | |||||||
| chr17:59804615 | T | TA | 154 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(151): Show |
154 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(151): Show |
intron_variant | MODIFIER | c.715-4159dupA | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr17 | 59804615 | ||||||
| chr17:59804615 | T | TAA | 6 | a0001c0001t0001g0103 a0001c0001t0001g0184 a0001c0001t0001g0198 others(3): Show |
6 | HG02145.hp1 HG02738.hp2 HG03471.hp2 others(3): Show |
intron_variant | MODIFIER | c.715-4160_715-4159d others(4): Show |
VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr17 | 59804615 | ||||||
| chr17:59804615 | TA | T | 7 | a0001c0001t0001g0079 a0001c0001t0002g0020 a0001c0001t0002g0023 others(4): Show |
7 | HG01168.hp1 HG02451.hp2 HG02698.hp2 others(4): Show |
intron_variant | MODIFIER | c.715-4159delA | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr17 | 59804615 | ||||||
| chr17:59804639 | T | G | 3 | a0001c0001t0002g0193 a0001c0001t0002g0196 a0001c0001t0002g0234 |
3 | HG01069.hp2 HG01071.hp2 HG01358.hp1 |
intron_variant | MODIFIER | c.715-4157T>G | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 7/11 | chr17 | 59804639 | |||||||
| chr17:59804676 | C | T | 1 | a0001c0001t0001g0106 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.715-4120C>T | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 7/11 | chr17 | 59804676 | |||||||
| chr17:59805150 | G | A | 1 | a0001c0001t0001g0202 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.715-3646G>A | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 7/11 | chr17 | 59805150 | |||||||
| chr17:59805156 | G | A | 1 | a0001c0001t0001g0177 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.715-3640G>A | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 7/11 | chr17 | 59805156 | |||||||
| chr17:59805313 | T | C | 62 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(59): Show |
62 | HG00438.hp2 HG00642.hp1 HG00673.hp2 others(59): Show |
intron_variant | MODIFIER | c.715-3483T>C | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 7/11 | chr17 | 59805313 | |||||||
| chr17:59805318 | C | A | 4 | a0001c0001t0001g0175 a0001c0001t0001g0220 a0001c0001t0001g0225 others(1): Show |
4 | HG00642.hp2 HG01978.hp2 HG01981.hp1 others(1): Show |
intron_variant | MODIFIER | c.715-3478C>A | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 7/11 | chr17 | 59805318 | |||||||
| chr17:59805388 | C | T | 2 | a0001c0001t0003g0113 a0001c0001t0009g0109 |
2 | HG00642.hp1 HG03831.hp2 |
intron_variant | MODIFIER | c.715-3408C>T | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 7/11 | chr17 | 59805388 | |||||||
| chr17:59806010 | T | G | 103 | a0001c0001t0001g0003 a0001c0001t0001g0076 a0001c0001t0001g0077 others(100): Show |
103 | HG00408.hp2 HG00423.hp2 HG00544.hp1 others(100): Show |
intron_variant | MODIFIER | c.715-2786T>G | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 7/11 | chr17 | 59806010 | |||||||
| chr17:59806153 | G | T | 1 | a0001c0001t0003g0137 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.715-2643G>T | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 7/11 | chr17 | 59806153 | |||||||
| chr17:59806266 | A | G | 1 | a0001c0001t0001g0277 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.715-2530A>G | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 7/11 | chr17 | 59806266 | |||||||
| chr17:59806285 | T | C | 87 | a0001c0001t0001g0100 a0001c0001t0001g0101 a0001c0001t0001g0102 others(84): Show |
87 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(84): Show |
intron_variant | MODIFIER | c.715-2511T>C | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 7/11 | chr17 | 59806285 | |||||||
| chr17:59806452 | G | T | 1 | a0001c0001t0003g0261 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.715-2344G>T | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 7/11 | chr17 | 59806452 | |||||||
| chr17:59806461 | C | T | 1 | a0001c0001t0002g0075 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.715-2335C>T | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 7/11 | chr17 | 59806461 | |||||||
| chr17:59806561 | A | C | 1 | a0001c0001t0001g0088 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.715-2235A>C | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 7/11 | chr17 | 59806561 | |||||||
| chr17:59806600 | A | G | 1 | a0001c0001t0002g0098 | 1 | NA18992.hp1 | intron_variant | MODIFIER | c.715-2196A>G | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 7/11 | chr17 | 59806600 | |||||||
| chr17:59806715 | C | CA | 124 | a0001c0001t0001g0003 a0001c0001t0001g0076 a0001c0001t0001g0077 others(121): Show |
124 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(121): Show |
intron_variant | MODIFIER | c.715-2064dupA | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr17 | 59806715 | ||||||
| chr17:59806715 | CA | C | 9 | a0001c0001t0001g0158 a0001c0001t0001g0165 a0001c0001t0001g0171 others(6): Show |
9 | HG00639.hp2 HG01891.hp1 HG01934.hp1 others(6): Show |
intron_variant | MODIFIER | c.715-2064delA | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr17 | 59806715 | ||||||
| chr17:59806895 | T | C | 1 | a0001c0001t0003g0149 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.715-1901T>C | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 7/11 | chr17 | 59806895 | |||||||
| chr17:59806899 | T | C | 1 | a0001c0001t0001g0282 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.715-1897T>C | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 7/11 | chr17 | 59806899 | |||||||
| chr17:59807036 | T | A | 177 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(174): Show |
177 | HG00408.hp2 HG00423.hp2 HG00438.hp2 others(174): Show |
intron_variant | MODIFIER | c.715-1760T>A | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 7/11 | chr17 | 59807036 | |||||||
| chr17:59807199 | G | GT | 32 | a0001c0001t0001g0069 a0001c0001t0001g0080 a0001c0001t0001g0090 others(29): Show |
32 | HG00741.hp1 HG01243.hp2 HG01934.hp2 others(29): Show |
intron_variant | MODIFIER | c.715-1582dupT | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr17 | 59807199 | ||||||
| chr17:59807199 | G | T | 6 | a0001c0001t0001g0204 a0001c0001t0001g0238 a0001c0001t0001g0280 others(3): Show |
6 | HG02145.hp2 HG02818.hp1 HG02922.hp2 others(3): Show |
intron_variant | MODIFIER | c.715-1597G>T | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 7/11 | chr17 | 59807199 | |||||||
| chr17:59807207 | T | G | 2 | a0001c0001t0001g0171 a0001c0001t0001g0172 |
2 | HG01891.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.715-1589T>G | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 7/11 | chr17 | 59807207 | |||||||
| chr17:59807223 | G | A | 11 | a0001c0001t0004g0262 a0001c0001t0004g0263 a0001c0001t0004g0265 others(8): Show |
11 | HG01109.hp2 HG02615.hp1 HG02896.hp1 others(8): Show |
intron_variant | MODIFIER | c.715-1573G>A | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 7/11 | chr17 | 59807223 | |||||||
| chr17:59807227 | C | T | 21 | a0001c0001t0001g0003 a0001c0001t0001g0076 a0001c0001t0001g0077 others(18): Show |
21 | HG01243.hp1 HG01891.hp2 HG02257.hp1 others(18): Show |
intron_variant | MODIFIER | c.715-1569C>T | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 7/11 | chr17 | 59807227 | |||||||
| chr17:59807232 | T | C | 11 | a0001c0001t0004g0262 a0001c0001t0004g0263 a0001c0001t0004g0265 others(8): Show |
11 | HG01109.hp2 HG02615.hp1 HG02896.hp1 others(8): Show |
intron_variant | MODIFIER | c.715-1564T>C | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 7/11 | chr17 | 59807232 | |||||||
| chr17:59807290 | C | A | 1 | a0001c0001t0003g0157 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.715-1506C>A | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 7/11 | chr17 | 59807290 | |||||||
| chr17:59807291 | G | T | 1 | a0001c0001t0003g0157 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.715-1505G>T | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 7/11 | chr17 | 59807291 | |||||||
| chr17:59807302 | A | G | 62 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(59): Show |
62 | HG00438.hp2 HG00642.hp1 HG00673.hp2 others(59): Show |
intron_variant | MODIFIER | c.715-1494A>G | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 7/11 | chr17 | 59807302 | |||||||
| chr17:59807497 | G | A | 1 | a0001c0001t0003g0108 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.715-1299G>A | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 7/11 | chr17 | 59807497 | |||||||
| chr17:59807507 | A | G | 62 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(59): Show |
62 | HG00438.hp2 HG00642.hp1 HG00673.hp2 others(59): Show |
intron_variant | MODIFIER | c.715-1289A>G | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 7/11 | chr17 | 59807507 | |||||||
| chr17:59807736 | G | A | 11 | a0001c0001t0004g0262 a0001c0001t0004g0263 a0001c0001t0004g0265 others(8): Show |
11 | HG01109.hp2 HG02615.hp1 HG02896.hp1 others(8): Show |
intron_variant | MODIFIER | c.715-1060G>A | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 7/11 | chr17 | 59807736 | |||||||
| chr17:59807741 | A | C | 25 | a0001c0001t0001g0003 a0001c0001t0001g0076 a0001c0001t0001g0077 others(22): Show |
25 | HG01243.hp1 HG01891.hp2 HG02109.hp2 others(22): Show |
intron_variant | MODIFIER | c.715-1055A>C | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 7/11 | chr17 | 59807741 | |||||||
| chr17:59807781 | A | G | 264 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(261): Show |
264 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(261): Show |
intron_variant | MODIFIER | c.715-1015A>G | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 7/11 | chr17 | 59807781 | |||||||
| chr17:59807832 | C | CA | 75 | a0001c0001t0001g0007 a0001c0001t0001g0152 a0001c0001t0002g0012 others(72): Show |
75 | HG00408.hp2 HG00423.hp2 HG00544.hp1 others(72): Show |
intron_variant | MODIFIER | c.715-945dupA | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr17 | 59807832 | ||||||
| chr17:59807832 | CA | C | 11 | a0001c0001t0001g0069 a0001c0001t0001g0204 a0001c0001t0001g0217 others(8): Show |
11 | HG01256.hp2 HG02145.hp2 HG02735.hp2 others(8): Show |
intron_variant | MODIFIER | c.715-945delA | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr17 | 59807832 | ||||||
| chr17:59807832 | CAAAAA | C | 51 | a0001c0001t0003g0105 a0001c0001t0003g0107 a0001c0001t0003g0108 others(48): Show |
51 | HG00438.hp2 HG00642.hp1 HG00673.hp2 others(48): Show |
intron_variant | MODIFIER | c.715-949_715-945del others(5): Show |
VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr17 | 59807832 | ||||||
| chr17:59808080 | A | T | 11 | a0001c0001t0004g0262 a0001c0001t0004g0263 a0001c0001t0004g0265 others(8): Show |
11 | HG01109.hp2 HG02615.hp1 HG02896.hp1 others(8): Show |
intron_variant | MODIFIER | c.715-716A>T | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 7/11 | chr17 | 59808080 | |||||||
| chr17:59808348 | C | T | 62 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(59): Show |
62 | HG00438.hp2 HG00642.hp1 HG00673.hp2 others(59): Show |
intron_variant | MODIFIER | c.715-448C>T | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 7/11 | chr17 | 59808348 | |||||||
| chr17:59808467 | T | C | 53 | a0001c0001t0003g0105 a0001c0001t0003g0107 a0001c0001t0003g0108 others(50): Show |
53 | HG00438.hp2 HG00642.hp1 HG00673.hp2 others(50): Show |
intron_variant | MODIFIER | c.715-329T>C | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 7/11 | chr17 | 59808467 | |||||||
| chr17:59808475 | C | T | 1 | a0001c0001t0001g0246 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.715-321C>T | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 7/11 | chr17 | 59808475 | |||||||
| chr17:59808540 | T | A | 103 | a0001c0001t0001g0003 a0001c0001t0001g0076 a0001c0001t0001g0077 others(100): Show |
103 | HG00408.hp2 HG00423.hp2 HG00544.hp1 others(100): Show |
intron_variant | MODIFIER | c.715-256T>A | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 7/11 | chr17 | 59808540 | |||||||
| chr17:59808764 | T | G | 103 | a0001c0001t0001g0003 a0001c0001t0001g0076 a0001c0001t0001g0077 others(100): Show |
103 | HG00408.hp2 HG00423.hp2 HG00544.hp1 others(100): Show |
intron_variant | MODIFIER | c.715-32T>G | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 7/11 | chr17 | 59808764 | |||||||
| chr17:59808766 | A | G | 11 | a0001c0001t0001g0076 a0001c0001t0001g0081 a0001c0001t0001g0082 others(8): Show |
11 | HG01891.hp2 HG02257.hp1 HG02280.hp2 others(8): Show |
intron_variant | MODIFIER | c.715-30A>G | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 7/11 | chr17 | 59808766 | |||||||
| chr17:59808977 | G | A | 1 | a0001c0001t0001g0176 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.795+101G>A | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 8/11 | chr17 | 59808977 | |||||||
| chr17:59809014 | T | C | 21 | a0001c0001t0001g0003 a0001c0001t0001g0076 a0001c0001t0001g0077 others(18): Show |
21 | HG01243.hp1 HG01891.hp2 HG02257.hp1 others(18): Show |
intron_variant | MODIFIER | c.795+138T>C | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 8/11 | chr17 | 59809014 | |||||||
| chr17:59809304 | C | CTT | 56 | a0001c0001t0001g0100 a0001c0001t0001g0101 a0001c0001t0001g0102 others(53): Show |
56 | HG00408.hp1 HG00423.hp1 HG00438.hp1 others(53): Show |
intron_variant | MODIFIER | c.795+455_795+456dup others(2): Show |
VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr17 | 59809304 | ||||||
| chr17:59809304 | C | CTTT | 27 | a0001c0001t0001g0103 a0001c0001t0001g0132 a0001c0001t0001g0175 others(24): Show |
27 | HG00280.hp1 HG00280.hp2 HG00544.hp2 others(24): Show |
intron_variant | MODIFIER | c.795+454_795+456dup others(3): Show |
VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr17 | 59809304 | ||||||
| chr17:59809304 | CT | C | 51 | a0001c0001t0001g0069 a0001c0001t0001g0070 a0001c0001t0001g0081 others(48): Show |
51 | HG00423.hp2 HG00438.hp2 HG00673.hp2 others(48): Show |
intron_variant | MODIFIER | c.795+456delT | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr17 | 59809304 | ||||||
| chr17:59809304 | CTT | C | 134 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(131): Show |
134 | HG00408.hp2 HG00544.hp1 HG00621.hp1 others(131): Show |
intron_variant | MODIFIER | c.795+455_795+456del others(2): Show |
VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr17 | 59809304 | ||||||
| chr17:59809332 | T | C | 1 | a0002c0003t0002g0030 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.795+456T>C | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 8/11 | chr17 | 59809332 | |||||||
| chr17:59809484 | A | AT | 45 | a0001c0001t0001g0070 a0001c0001t0001g0158 a0001c0001t0001g0159 others(42): Show |
45 | HG00140.hp1 HG00408.hp2 HG00423.hp2 others(42): Show |
intron_variant | MODIFIER | c.795+648dupT | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr17 | 59809484 | ||||||
| chr17:59809484 | A | ATT | 13 | a0001c0001t0002g0012 a0001c0001t0002g0015 a0001c0001t0002g0017 others(10): Show |
13 | HG01123.hp1 HG01981.hp2 HG02109.hp2 others(10): Show |
intron_variant | MODIFIER | c.795+647_795+648dup others(2): Show |
VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr17 | 59809484 | ||||||
| chr17:59809484 | A | ATTTT | 6 | a0001c0001t0001g0089 a0001c0001t0002g0014 a0001c0001t0006g0283 others(3): Show |
6 | HG00639.hp2 HG02486.hp2 HG03130.hp2 others(3): Show |
intron_variant | MODIFIER | c.795+645_795+648dup others(4): Show |
VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr17 | 59809484 | ||||||
| chr17:59809484 | A | ATTTTTTT others(3): Show |
1 | a0001c0001t0007g0274 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.795+639_795+648dup others(10): Show |
VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr17 | 59809484 | ||||||
| chr17:59809484 | A | ATTTTTTT others(4): Show |
1 | a0001c0001t0007g0275 | 1 | HG03492.hp1 | intron_variant | MODIFIER | c.795+638_795+648dup others(11): Show |
VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr17 | 59809484 | ||||||
| chr17:59809484 | A | ATTTTTTT others(6): Show |
1 | a0001c0001t0001g0076 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.795+636_795+648dup others(13): Show |
VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr17 | 59809484 | ||||||
| chr17:59809484 | A | ATTTTTTT others(7): Show |
2 | a0001c0001t0001g0003 a0001c0001t0001g0278 |
2 | HG02258.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.795+635_795+648dup others(14): Show |
VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr17 | 59809484 | ||||||
| chr17:59809484 | A | ATTTTTTT others(8): Show |
2 | a0001c0001t0001g0082 a0001c0001t0001g0087 |
2 | HG02559.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.795+634_795+648dup others(15): Show |
VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr17 | 59809484 | ||||||
| chr17:59809484 | ATTT | A | 13 | a0001c0001t0001g0277 a0001c0001t0003g0107 a0001c0001t0003g0113 others(10): Show |
13 | HG00438.hp2 HG00642.hp1 HG01168.hp2 others(10): Show |
intron_variant | MODIFIER | c.795+646_795+648del others(3): Show |
VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr17 | 59809484 | ||||||
| chr17:59809484 | ATTTT | A | 23 | a0001c0001t0003g0105 a0001c0001t0003g0110 a0001c0001t0003g0114 others(20): Show |
23 | HG00673.hp2 HG01261.hp1 HG01978.hp1 others(20): Show |
intron_variant | MODIFIER | c.795+645_795+648del others(4): Show |
VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr17 | 59809484 | ||||||
| chr17:59809484 | ATTTTT | A | 18 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(15): Show |
18 | HG00738.hp2 HG01069.hp1 HG01071.hp1 others(15): Show |
intron_variant | MODIFIER | c.795+644_795+648del others(5): Show |
VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr17 | 59809484 | ||||||
| chr17:59809484 | ATTTTTTT others(1): Show |
A | 10 | a0001c0001t0001g0077 a0001c0001t0001g0078 a0001c0001t0001g0080 others(7): Show |
10 | HG01243.hp1 HG02615.hp1 HG02630.hp1 others(7): Show |
intron_variant | MODIFIER | c.795+641_795+648del others(8): Show |
VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr17 | 59809484 | ||||||
| chr17:59809484 | ATTTTTTT others(2): Show |
A | 6 | a0001c0001t0001g0079 a0001c0001t0004g0262 a0001c0001t0004g0263 others(3): Show |
6 | HG01109.hp2 HG02451.hp2 HG02970.hp1 others(3): Show |
intron_variant | MODIFIER | c.795+640_795+648del others(9): Show |
VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr17 | 59809484 | ||||||
| chr17:59809484 | ATTTTTTT others(3): Show |
A | 1 | a0001c0001t0001g0090 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.795+639_795+648del others(10): Show |
VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr17 | 59809484 | ||||||
| chr17:59809484 | ATTTTTTT others(5): Show |
A | 2 | a0001c0001t0001g0088 a0001c0001t0001g0165 |
2 | HG02559.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.795+637_795+648del others(12): Show |
VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr17 | 59809484 | ||||||
| chr17:59809484 | ATTTTTTT others(6): Show |
A | 2 | a0001c0001t0001g0171 a0001c0001t0001g0172 |
2 | HG01891.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.795+636_795+648del others(13): Show |
VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr17 | 59809484 | ||||||
| chr17:59809484 | ATTTTTTT others(11): Show |
A | 12 | a0001c0001t0001g0103 a0001c0001t0001g0184 a0001c0001t0001g0198 others(9): Show |
12 | HG00544.hp2 HG00621.hp2 HG00741.hp2 others(9): Show |
intron_variant | MODIFIER | c.795+631_795+648del others(18): Show |
VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr17 | 59809484 | ||||||
| chr17:59809484 | ATTTTTTT others(12): Show |
A | 74 | a0001c0001t0001g0100 a0001c0001t0001g0101 a0001c0001t0001g0102 others(71): Show |
74 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(71): Show |
intron_variant | MODIFIER | c.795+630_795+648del others(19): Show |
VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr17 | 59809484 | ||||||
| chr17:59809484 | ATTTTTTT others(13): Show |
A | 1 | a0001c0001t0001g0201 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.795+629_795+648del others(20): Show |
VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr17 | 59809484 | ||||||
| chr17:59809530 | G | A | 11 | a0001c0001t0004g0262 a0001c0001t0004g0263 a0001c0001t0004g0265 others(8): Show |
11 | HG01109.hp2 HG02615.hp1 HG02896.hp1 others(8): Show |
intron_variant | MODIFIER | c.795+654G>A | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 8/11 | chr17 | 59809530 | |||||||
| chr17:59809554 | G | T | 177 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(174): Show |
177 | HG00408.hp2 HG00423.hp2 HG00438.hp2 others(174): Show |
intron_variant | MODIFIER | c.795+678G>T | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 8/11 | chr17 | 59809554 | |||||||
| chr17:59809737 | A | G | 1 | a0001c0001t0001g0248 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.795+861A>G | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 8/11 | chr17 | 59809737 | |||||||
| chr17:59809851 | A | C | 1 | a0001c0001t0002g0236 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.795+975A>C | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 8/11 | chr17 | 59809851 | |||||||
| chr17:59810210 | G | A | 1 | a0001c0001t0001g0277 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.795+1334G>A | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 8/11 | chr17 | 59810210 | |||||||
| chr17:59810406 | G | A | 1 | a0001c0001t0001g0250 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.796-1264G>A | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 8/11 | chr17 | 59810406 | |||||||
| chr17:59810591 | G | A | 78 | a0001c0001t0002g0012 a0001c0001t0002g0013 a0001c0001t0002g0014 others(75): Show |
78 | HG00408.hp2 HG00423.hp2 HG00544.hp1 others(75): Show |
intron_variant | MODIFIER | c.796-1079G>A | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 8/11 | chr17 | 59810591 | |||||||
| chr17:59811065 | G | A | 2 | a0001c0001t0003g0140 a0001c0001t0003g0145 |
2 | HG02717.hp1 HG02895.hp2 |
intron_variant | MODIFIER | c.796-605G>A | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 8/11 | chr17 | 59811065 | |||||||
| chr17:59811405 | G | A | 1 | a0001c0001t0014g0189 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.796-265G>A | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 8/11 | chr17 | 59811405 | |||||||
| chr17:59811831 | T | G | 78 | a0001c0001t0001g0100 a0001c0001t0001g0101 a0001c0001t0001g0102 others(75): Show |
78 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(75): Show |
intron_variant | MODIFIER | c.912+45T>G | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 9/11 | chr17 | 59811831 | |||||||
| chr17:59812044 | T | G | 177 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(174): Show |
177 | HG00408.hp2 HG00423.hp2 HG00438.hp2 others(174): Show |
intron_variant | MODIFIER | c.912+258T>G | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 9/11 | chr17 | 59812044 | |||||||
| chr17:59812045 | T | A | 177 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(174): Show |
177 | HG00408.hp2 HG00423.hp2 HG00438.hp2 others(174): Show |
intron_variant | MODIFIER | c.912+259T>A | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 9/11 | chr17 | 59812045 | |||||||
| chr17:59812322 | G | T | 1 | a0001c0001t0003g0113 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.912+536G>T | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 9/11 | chr17 | 59812322 | |||||||
| chr17:59812460 | G | A | 2 | a0001c0001t0001g0153 a0001c0001t0001g0170 |
2 | HG03041.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.912+674G>A | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 9/11 | chr17 | 59812460 | |||||||
| chr17:59812624 | G | A | 78 | a0001c0001t0002g0012 a0001c0001t0002g0013 a0001c0001t0002g0014 others(75): Show |
78 | HG00408.hp2 HG00423.hp2 HG00544.hp1 others(75): Show |
intron_variant | MODIFIER | c.912+838G>A | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 9/11 | chr17 | 59812624 | |||||||
| chr17:59812888 | G | A | 1 | a0001c0001t0002g0094 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.912+1102G>A | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 9/11 | chr17 | 59812888 | |||||||
| chr17:59813007 | A | G | 1 | a0001c0001t0002g0063 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.912+1221A>G | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 9/11 | chr17 | 59813007 | |||||||
| chr17:59813133 | C | T | 1 | a0001c0001t0001g0246 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.912+1347C>T | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 9/11 | chr17 | 59813133 | |||||||
| chr17:59813215 | T | C | 1 | a0001c0001t0001g0203 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.912+1429T>C | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 9/11 | chr17 | 59813215 | |||||||
| chr17:59813268 | C | T | 53 | a0001c0001t0003g0105 a0001c0001t0003g0107 a0001c0001t0003g0108 others(50): Show |
53 | HG00438.hp2 HG00642.hp1 HG00673.hp2 others(50): Show |
intron_variant | MODIFIER | c.912+1482C>T | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 9/11 | chr17 | 59813268 | |||||||
| chr17:59813571 | C | CA | 97 | a0001c0001t0001g0003 a0001c0001t0001g0076 a0001c0001t0001g0077 others(94): Show |
97 | HG00408.hp2 HG00423.hp2 HG00544.hp1 others(94): Show |
intron_variant | MODIFIER | c.912+1800dupA | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 9/11 | INFO_REALIGN_3_PRIME | chr17 | 59813571 | ||||||
| chr17:59813789 | A | G | 1 | a0001c0001t0004g0267 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.912+2003A>G | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 9/11 | chr17 | 59813789 | |||||||
| chr17:59813846 | T | C | 53 | a0001c0001t0003g0105 a0001c0001t0003g0107 a0001c0001t0003g0108 others(50): Show |
53 | HG00438.hp2 HG00642.hp1 HG00673.hp2 others(50): Show |
intron_variant | MODIFIER | c.912+2060T>C | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 9/11 | chr17 | 59813846 | |||||||
| chr17:59813943 | T | G | 1 | a0001c0001t0001g0095 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.912+2157T>G | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 9/11 | chr17 | 59813943 | |||||||
| chr17:59813974 | A | ATGATTGA others(1): Show |
264 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(261): Show |
264 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(261): Show |
intron_variant | MODIFIER | c.912+2202_912+2209d others(10): Show |
VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 9/11 | INFO_REALIGN_3_PRIME | chr17 | 59813974 | ||||||
| chr17:59813974 | A | ATGATTGA others(5): Show |
2 | a0001c0001t0001g0254 a0001c0001t0003g0131 |
2 | NA18959.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.912+2198_912+2209d others(14): Show |
VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 9/11 | INFO_REALIGN_3_PRIME | chr17 | 59813974 | ||||||
| chr17:59814215 | G | A | 1 | a0001c0001t0003g0157 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.912+2429G>A | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 9/11 | chr17 | 59814215 | |||||||
| chr17:59814236 | C | T | 1 | a0001c0001t0004g0273 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.912+2450C>T | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 9/11 | chr17 | 59814236 | |||||||
| chr17:59814267 | G | A | 1 | a0001c0001t0001g0095 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.912+2481G>A | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 9/11 | chr17 | 59814267 | |||||||
| chr17:59814278 | A | C | 1 | a0001c0001t0004g0268 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.912+2492A>C | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 9/11 | chr17 | 59814278 | |||||||
| chr17:59815259 | T | TTAGAAAA others(322): Show |
1 | a0001c0001t0006g0284 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.913-2438_913-2437i others(331): Show |
VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 9/11 | INFO_REALIGN_3_PRIME | chr17 | 59815259 | ||||||
| chr17:59815259 | T | TTAGAAAA others(323): Show |
1 | a0001c0001t0006g0283 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.913-2438_913-2437i others(332): Show |
VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 9/11 | INFO_REALIGN_3_PRIME | chr17 | 59815259 | ||||||
| chr17:59815279 | A | T | 78 | a0001c0001t0002g0012 a0001c0001t0002g0013 a0001c0001t0002g0014 others(75): Show |
78 | HG00408.hp2 HG00423.hp2 HG00544.hp1 others(75): Show |
intron_variant | MODIFIER | c.913-2433A>T | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 9/11 | chr17 | 59815279 | |||||||
| chr17:59815464 | ATTT | A | 103 | a0001c0001t0001g0003 a0001c0001t0001g0076 a0001c0001t0001g0077 others(100): Show |
103 | HG00408.hp2 HG00423.hp2 HG00544.hp1 others(100): Show |
intron_variant | MODIFIER | c.913-2245_913-2243d others(5): Show |
VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 9/11 | INFO_REALIGN_3_PRIME | chr17 | 59815464 | ||||||
| chr17:59815468 | T | A | 103 | a0001c0001t0001g0003 a0001c0001t0001g0076 a0001c0001t0001g0077 others(100): Show |
103 | HG00408.hp2 HG00423.hp2 HG00544.hp1 others(100): Show |
intron_variant | MODIFIER | c.913-2244T>A | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 9/11 | chr17 | 59815468 | |||||||
| chr17:59815573 | G | A | 1 | a0001c0001t0003g0121 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.913-2139G>A | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 9/11 | chr17 | 59815573 | |||||||
| chr17:59815689 | TA | T | 177 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(174): Show |
177 | HG00408.hp2 HG00423.hp2 HG00438.hp2 others(174): Show |
intron_variant | MODIFIER | c.913-2015delA | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 9/11 | INFO_REALIGN_3_PRIME | chr17 | 59815689 | ||||||
| chr17:59815788 | G | A | 63 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(60): Show |
63 | HG00438.hp2 HG00642.hp1 HG00673.hp2 others(60): Show |
intron_variant | MODIFIER | c.913-1924G>A | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 9/11 | chr17 | 59815788 | |||||||
| chr17:59815804 | C | G | 1 | a0001c0001t0001g0077 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.913-1908C>G | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 9/11 | chr17 | 59815804 | |||||||
| chr17:59815850 | C | T | 1 | a0001c0001t0001g0207 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.913-1862C>T | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 9/11 | chr17 | 59815850 | |||||||
| chr17:59815855 | C | CA | 63 | a0001c0001t0001g0069 a0001c0001t0001g0150 a0001c0001t0001g0210 others(60): Show |
63 | HG00438.hp2 HG00642.hp1 HG00673.hp2 others(60): Show |
intron_variant | MODIFIER | c.913-1836dupA | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 9/11 | INFO_REALIGN_3_PRIME | chr17 | 59815855 | ||||||
| chr17:59815855 | C | CAA | 82 | a0001c0001t0001g0070 a0001c0001t0001g0095 a0001c0001t0001g0100 others(79): Show |
82 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(79): Show |
intron_variant | MODIFIER | c.913-1837_913-1836d others(4): Show |
VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 9/11 | INFO_REALIGN_3_PRIME | chr17 | 59815855 | ||||||
| chr17:59815855 | C | CAAA | 8 | a0001c0001t0001g0103 a0001c0001t0001g0106 a0001c0001t0001g0177 others(5): Show |
8 | HG00408.hp1 HG00438.hp1 HG00639.hp1 others(5): Show |
intron_variant | MODIFIER | c.913-1838_913-1836d others(5): Show |
VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 9/11 | INFO_REALIGN_3_PRIME | chr17 | 59815855 | ||||||
| chr17:59815855 | CAAAAAAA others(5): Show |
C | 78 | a0001c0001t0002g0012 a0001c0001t0002g0013 a0001c0001t0002g0014 others(75): Show |
78 | HG00408.hp2 HG00423.hp2 HG00544.hp1 others(75): Show |
intron_variant | MODIFIER | c.913-1847_913-1836d others(14): Show |
VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 9/11 | INFO_REALIGN_3_PRIME | chr17 | 59815855 | ||||||
| chr17:59815934 | A | G | 5 | a0001c0001t0002g0024 a0001c0001t0002g0025 a0001c0001t0002g0026 others(2): Show |
5 | NA18977.hp2 NA19057.hp2 NA19060.hp1 others(2): Show |
intron_variant | MODIFIER | c.913-1778A>G | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 9/11 | chr17 | 59815934 | |||||||
| chr17:59816305 | T | G | 1 | a0001c0001t0005g0018 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.913-1407T>G | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 9/11 | chr17 | 59816305 | |||||||
| chr17:59816599 | A | T | 1 | a0001c0001t0002g0036 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.913-1113A>T | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 9/11 | chr17 | 59816599 | |||||||
| chr17:59816660 | C | T | 1 | a0001c0001t0003g0118 | 1 | NA19086.hp2 | intron_variant | MODIFIER | c.913-1052C>T | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 9/11 | chr17 | 59816660 | |||||||
| chr17:59816661 | C | T | 1 | a0001c0001t0001g0237 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.913-1051C>T | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 9/11 | chr17 | 59816661 | |||||||
| chr17:59816815 | G | A | 1 | a0001c0001t0001g0203 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.913-897G>A | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 9/11 | chr17 | 59816815 | |||||||
| chr17:59816869 | C | G | 54 | a0001c0001t0001g0277 a0001c0001t0003g0105 a0001c0001t0003g0107 others(51): Show |
54 | HG00438.hp2 HG00642.hp1 HG00673.hp2 others(51): Show |
intron_variant | MODIFIER | c.913-843C>G | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 9/11 | chr17 | 59816869 | |||||||
| chr17:59816902 | C | A | 1 | a0001c0001t0004g0273 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.913-810C>A | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 9/11 | chr17 | 59816902 | |||||||
| chr17:59816945 | CA | C | 52 | a0001c0001t0003g0107 a0001c0001t0003g0108 a0001c0001t0003g0110 others(49): Show |
52 | HG00438.hp2 HG00642.hp1 HG00673.hp2 others(49): Show |
intron_variant | MODIFIER | c.913-754delA | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 9/11 | INFO_REALIGN_3_PRIME | chr17 | 59816945 | ||||||
| chr17:59816974 | G | GA | 6 | a0001c0001t0002g0014 a0001c0001t0003g0138 a0001c0001t0006g0283 others(3): Show |
6 | HG02109.hp2 HG03130.hp2 HG06807.hp2 others(3): Show |
intron_variant | MODIFIER | c.913-727dupA | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 9/11 | INFO_REALIGN_3_PRIME | chr17 | 59816974 | ||||||
| chr17:59816974 | GA | G | 11 | a0001c0001t0004g0262 a0001c0001t0004g0263 a0001c0001t0004g0265 others(8): Show |
11 | HG01109.hp2 HG02615.hp1 HG02896.hp1 others(8): Show |
intron_variant | MODIFIER | c.913-727delA | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 9/11 | INFO_REALIGN_3_PRIME | chr17 | 59816974 | ||||||
| chr17:59817098 | A | G | 119 | a0001c0001t0001g0069 a0001c0001t0001g0070 a0001c0001t0001g0095 others(116): Show |
119 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(116): Show |
intron_variant | MODIFIER | c.913-614A>G | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 9/11 | chr17 | 59817098 | |||||||
| chr17:59817231 | G | T | 1 | a0001c0001t0003g0120 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.913-481G>T | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 9/11 | chr17 | 59817231 | |||||||
| chr17:59817246 | CCTGGGCA others(1): Show |
C | 181 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(178): Show |
181 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(178): Show |
intron_variant | MODIFIER | c.913-457_913-450del others(8): Show |
VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 9/11 | INFO_REALIGN_3_PRIME | chr17 | 59817246 | ||||||
| chr17:59817282 | C | CA | 11 | a0001c0001t0001g0103 a0001c0001t0001g0247 a0001c0001t0001g0254 others(8): Show |
11 | HG01123.hp1 HG02145.hp2 HG02738.hp1 others(8): Show |
intron_variant | MODIFIER | c.913-408dupA | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 9/11 | INFO_REALIGN_3_PRIME | chr17 | 59817282 | ||||||
| chr17:59817282 | CA | C | 65 | a0001c0001t0001g0150 a0001c0001t0002g0020 a0001c0001t0002g0037 others(62): Show |
65 | HG00438.hp2 HG00642.hp1 HG00673.hp2 others(62): Show |
intron_variant | MODIFIER | c.913-408delA | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 9/11 | INFO_REALIGN_3_PRIME | chr17 | 59817282 | ||||||
| chr17:59817282 | CAA | C | 24 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(21): Show |
24 | HG00140.hp1 HG01099.hp1 HG01109.hp1 others(21): Show |
intron_variant | MODIFIER | c.913-409_913-408del others(2): Show |
VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 9/11 | INFO_REALIGN_3_PRIME | chr17 | 59817282 | ||||||
| chr17:59817342 | C | CTTTTA | 107 | a0001c0001t0001g0069 a0001c0001t0001g0070 a0001c0001t0001g0100 others(104): Show |
107 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(104): Show |
intron_variant | MODIFIER | c.913-350_913-346dup others(5): Show |
VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 9/11 | INFO_REALIGN_3_PRIME | chr17 | 59817342 | ||||||
| chr17:59817434 | C | T | 11 | a0001c0001t0004g0262 a0001c0001t0004g0263 a0001c0001t0004g0265 others(8): Show |
11 | HG01109.hp2 HG02615.hp1 HG02896.hp1 others(8): Show |
intron_variant | MODIFIER | c.913-278C>T | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 9/11 | chr17 | 59817434 | |||||||
| chr17:59817459 | C | T | 1 | a0001c0001t0001g0248 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.913-253C>T | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 9/11 | chr17 | 59817459 | |||||||
| chr17:59817524 | G | A | 1 | a0001c0001t0001g0213 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.913-188G>A | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 9/11 | chr17 | 59817524 | |||||||
| chr17:59817660 | GTTGGTTT | G | 8 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(5): Show |
8 | HG01099.hp1 HG01884.hp1 HG01952.hp2 others(5): Show |
intron_variant | MODIFIER | c.913-49_913-43delGG others(5): Show |
VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 9/11 | INFO_REALIGN_3_PRIME | chr17 | 59817660 | ||||||
| chr17:59817664 | G | T | 15 | a0001c0001t0001g0150 a0001c0001t0001g0153 a0001c0001t0001g0158 others(12): Show |
15 | HG00140.hp1 HG01109.hp1 HG01255.hp1 others(12): Show |
intron_variant | MODIFIER | c.913-48G>T | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 9/11 | chr17 | 59817664 | |||||||
| chr17:59818303 | G | T | 1 | a0001c0001t0001g0219 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.974+530G>T | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 10/11 | chr17 | 59818303 | |||||||
| chr17:59818549 | T | C | 1 | a0001c0001t0001g0090 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.974+776T>C | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 10/11 | chr17 | 59818549 | |||||||
| chr17:59818580 | C | G | 119 | a0001c0001t0001g0069 a0001c0001t0001g0070 a0001c0001t0001g0095 others(116): Show |
119 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(116): Show |
intron_variant | MODIFIER | c.974+807C>G | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 10/11 | chr17 | 59818580 | |||||||
| chr17:59818595 | A | C | 62 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(59): Show |
62 | HG00438.hp2 HG00642.hp1 HG00673.hp2 others(59): Show |
intron_variant | MODIFIER | c.974+822A>C | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 10/11 | chr17 | 59818595 | |||||||
| chr17:59818661 | G | T | 181 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(178): Show |
181 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(178): Show |
intron_variant | MODIFIER | c.974+888G>T | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 10/11 | chr17 | 59818661 | |||||||
| chr17:59818667 | G | A | 1 | a0001c0001t0001g0004 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.974+894G>A | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 10/11 | chr17 | 59818667 | |||||||
| chr17:59818859 | T | A | 119 | a0001c0001t0001g0069 a0001c0001t0001g0070 a0001c0001t0001g0095 others(116): Show |
119 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(116): Show |
intron_variant | MODIFIER | c.974+1086T>A | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 10/11 | chr17 | 59818859 | |||||||
| chr17:59818977 | C | T | 119 | a0001c0001t0001g0069 a0001c0001t0001g0070 a0001c0001t0001g0095 others(116): Show |
119 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(116): Show |
intron_variant | MODIFIER | c.974+1204C>T | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 10/11 | chr17 | 59818977 | |||||||
| chr17:59819024 | T | G | 3 | a0001c0001t0001g0206 a0001c0001t0001g0209 a0001c0001t0001g0224 |
3 | HG00621.hp2 HG02040.hp1 HG02129.hp2 |
intron_variant | MODIFIER | c.974+1251T>G | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 10/11 | chr17 | 59819024 | |||||||
| chr17:59819372 | G | A | 1 | a0001c0001t0004g0271 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.974+1599G>A | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 10/11 | chr17 | 59819372 | |||||||
| chr17:59819464 | TTTG | T | 8 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(5): Show |
8 | HG01099.hp1 HG01884.hp1 HG01952.hp2 others(5): Show |
intron_variant | MODIFIER | c.974+1700_974+1702d others(5): Show |
VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr17 | 59819464 | ||||||
| chr17:59819528 | A | G | 1 | a0001c0001t0002g0074 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.974+1755A>G | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 10/11 | chr17 | 59819528 | |||||||
| chr17:59819546 | C | G | 18 | a0001c0001t0001g0150 a0001c0001t0001g0153 a0001c0001t0001g0158 others(15): Show |
18 | HG00140.hp1 HG01109.hp1 HG01255.hp1 others(15): Show |
intron_variant | MODIFIER | c.974+1773C>G | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 10/11 | chr17 | 59819546 | |||||||
| chr17:59819602 | C | T | 2 | a0001c0001t0003g0111 a0001c0001t0003g0112 |
2 | HG01071.hp1 HG03834.hp1 |
intron_variant | MODIFIER | c.974+1829C>T | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 10/11 | chr17 | 59819602 | |||||||
| chr17:59819742 | G | A | 7 | a0001c0001t0001g0201 a0001c0001t0001g0204 a0001c0001t0001g0238 others(4): Show |
7 | HG02145.hp2 HG02818.hp1 HG02886.hp1 others(4): Show |
intron_variant | MODIFIER | c.974+1969G>A | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 10/11 | chr17 | 59819742 | |||||||
| chr17:59820248 | C | T | 53 | a0001c0001t0003g0105 a0001c0001t0003g0107 a0001c0001t0003g0108 others(50): Show |
53 | HG00438.hp2 HG00642.hp1 HG00673.hp2 others(50): Show |
intron_variant | MODIFIER | c.974+2475C>T | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 10/11 | chr17 | 59820248 | |||||||
| chr17:59820624 | T | C | 1 | a0001c0001t0002g0063 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.974+2851T>C | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 10/11 | chr17 | 59820624 | |||||||
| chr17:59820974 | G | GT | 17 | a0001c0001t0001g0089 a0001c0001t0001g0175 a0001c0001t0001g0200 others(14): Show |
17 | HG00280.hp2 HG01884.hp2 HG01981.hp1 others(14): Show |
intron_variant | MODIFIER | c.974+3215dupT | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr17 | 59820974 | ||||||
| chr17:59820974 | G | T | 12 | a0001c0001t0002g0236 a0001c0001t0004g0262 a0001c0001t0004g0263 others(9): Show |
12 | HG01109.hp2 HG02615.hp1 HG02896.hp1 others(9): Show |
intron_variant | MODIFIER | c.974+3201G>T | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 10/11 | chr17 | 59820974 | |||||||
| chr17:59821430 | T | C | 1 | a0001c0001t0002g0037 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.974+3657T>C | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 10/11 | chr17 | 59821430 | |||||||
| chr17:59821539 | C | CT | 15 | a0001c0001t0001g0087 a0001c0001t0002g0015 a0001c0001t0002g0017 others(12): Show |
15 | HG00741.hp1 HG01069.hp2 HG01123.hp1 others(12): Show |
intron_variant | MODIFIER | c.974+3789dupT | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr17 | 59821539 | ||||||
| chr17:59821539 | C | CTTTTTT | 9 | a0001c0001t0004g0262 a0001c0001t0004g0263 a0001c0001t0004g0265 others(6): Show |
9 | HG01109.hp2 HG02615.hp1 HG02896.hp1 others(6): Show |
intron_variant | MODIFIER | c.974+3784_974+3789d others(8): Show |
VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr17 | 59821539 | ||||||
| chr17:59821539 | CT | C | 16 | a0001c0001t0001g0003 a0001c0001t0001g0077 a0001c0001t0001g0078 others(13): Show |
16 | HG01243.hp1 HG01891.hp2 HG02258.hp2 others(13): Show |
intron_variant | MODIFIER | c.974+3789delT | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr17 | 59821539 | ||||||
| chr17:59821539 | CTTTTTT | C | 103 | a0001c0001t0001g0069 a0001c0001t0001g0070 a0001c0001t0001g0100 others(100): Show |
103 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(100): Show |
intron_variant | MODIFIER | c.974+3784_974+3789d others(8): Show |
VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr17 | 59821539 | ||||||
| chr17:59821539 | CTTTTTTT | C | 62 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(59): Show |
62 | HG00438.hp2 HG00642.hp1 HG00673.hp2 others(59): Show |
intron_variant | MODIFIER | c.974+3783_974+3789d others(9): Show |
VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr17 | 59821539 | ||||||
| chr17:59822326 | C | CT | 28 | a0001c0001t0001g0158 a0001c0001t0001g0159 a0001c0001t0001g0160 others(25): Show |
28 | HG00438.hp2 HG01255.hp1 HG01256.hp1 others(25): Show |
intron_variant | MODIFIER | c.974+4571dupT | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr17 | 59822326 | ||||||
| chr17:59822326 | C | CTT | 76 | a0001c0001t0001g0069 a0001c0001t0001g0070 a0001c0001t0001g0100 others(73): Show |
76 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(73): Show |
intron_variant | MODIFIER | c.974+4570_974+4571d others(4): Show |
VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr17 | 59822326 | ||||||
| chr17:59822326 | C | CTTT | 7 | a0001c0001t0001g0103 a0001c0001t0001g0175 a0001c0001t0001g0176 others(4): Show |
7 | HG01074.hp2 HG01361.hp2 HG01981.hp1 others(4): Show |
intron_variant | MODIFIER | c.974+4569_974+4571d others(5): Show |
VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr17 | 59822326 | ||||||
| chr17:59822415 | G | A | 1 | a0001c0001t0001g0095 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.974+4642G>A | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 10/11 | chr17 | 59822415 | |||||||
| chr17:59822784 | A | T | 3 | a0001c0001t0001g0182 a0001c0001t0001g0183 a0001c0001t0001g0184 |
3 | HG02602.hp1 HG03704.hp1 HG03831.hp1 |
intron_variant | MODIFIER | c.974+5011A>T | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 10/11 | chr17 | 59822784 | |||||||
| chr17:59822965 | A | G | 1 | a0001c0001t0001g0175 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.974+5192A>G | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 10/11 | chr17 | 59822965 | |||||||
| chr17:59823300 | A | C | 1 | a0001c0001t0001g0199 | 1 | HG02273.hp2 | intron_variant | MODIFIER | c.974+5527A>C | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 10/11 | chr17 | 59823300 | |||||||
| chr17:59823447 | CA | C | 112 | a0001c0001t0001g0069 a0001c0001t0001g0070 a0001c0001t0001g0095 others(109): Show |
112 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(109): Show |
intron_variant | MODIFIER | c.974+5691delA | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr17 | 59823447 | ||||||
| chr17:59823524 | C | T | 1 | a0001c0001t0001g0217 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.974+5751C>T | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 10/11 | chr17 | 59823524 | |||||||
| chr17:59823562 | A | C | 1 | a0001c0001t0003g0117 | 1 | NA18991.hp2 | intron_variant | MODIFIER | c.974+5789A>C | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 10/11 | chr17 | 59823562 | |||||||
| chr17:59823608 | C | T | 10 | a0001c0001t0002g0014 a0001c0001t0002g0031 a0001c0001t0002g0040 others(7): Show |
10 | NA18949.hp1 NA18963.hp1 NA18964.hp2 others(7): Show |
intron_variant | MODIFIER | c.974+5835C>T | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 10/11 | chr17 | 59823608 | |||||||
| chr17:59823609 | G | A | 1 | a0001c0001t0001g0277 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.974+5836G>A | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 10/11 | chr17 | 59823609 | |||||||
| chr17:59823682 | C | T | 11 | a0001c0001t0004g0262 a0001c0001t0004g0263 a0001c0001t0004g0265 others(8): Show |
11 | HG01109.hp2 HG02615.hp1 HG02896.hp1 others(8): Show |
intron_variant | MODIFIER | c.974+5909C>T | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 10/11 | chr17 | 59823682 | |||||||
| chr17:59823754 | A | C | 1 | a0001c0001t0001g0103 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.974+5981A>C | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 10/11 | chr17 | 59823754 | |||||||
| chr17:59823990 | G | A | 1 | a0001c0001t0001g0250 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.974+6217G>A | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 10/11 | chr17 | 59823990 | |||||||
| chr17:59824131 | G | A | 1 | a0001c0001t0001g0250 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.974+6358G>A | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 10/11 | chr17 | 59824131 | |||||||
| chr17:59824251 | C | CA | 15 | a0001c0001t0001g0088 a0001c0001t0001g0150 a0001c0001t0002g0049 others(12): Show |
15 | HG00544.hp1 HG00741.hp2 HG01109.hp2 others(12): Show |
intron_variant | MODIFIER | c.974+6492dupA | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr17 | 59824251 | ||||||
| chr17:59824251 | CA | C | 55 | a0001c0001t0001g0095 a0001c0001t0001g0214 a0001c0001t0001g0277 others(52): Show |
55 | HG00642.hp1 HG00673.hp2 HG00738.hp2 others(52): Show |
intron_variant | MODIFIER | c.974+6492delA | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr17 | 59824251 | ||||||
| chr17:59824253 | A | G | 5 | a0001c0001t0001g0153 a0001c0001t0001g0168 a0001c0001t0001g0169 others(2): Show |
5 | HG00140.hp1 HG01109.hp1 HG03041.hp1 others(2): Show |
intron_variant | MODIFIER | c.974+6480A>G | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 10/11 | chr17 | 59824253 | |||||||
| chr17:59824264 | A | G | 2 | a0001c0001t0006g0285 a0001c0001t0006g0286 |
2 | HG02109.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.974+6491A>G | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 10/11 | chr17 | 59824264 | |||||||
| chr17:59824265 | A | G | 3 | a0001c0001t0006g0284 a0001c0001t0006g0285 a0001c0001t0006g0286 |
3 | HG02109.hp2 HG03130.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.974+6492A>G | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 10/11 | chr17 | 59824265 | |||||||
| chr17:59824291 | G | A | 89 | a0001c0001t0001g0069 a0001c0001t0001g0070 a0001c0001t0001g0100 others(86): Show |
89 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(86): Show |
intron_variant | MODIFIER | c.974+6518G>A | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 10/11 | chr17 | 59824291 | |||||||
| chr17:59824398 | C | T | 8 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(5): Show |
8 | HG01099.hp1 HG01884.hp1 HG01952.hp2 others(5): Show |
intron_variant | MODIFIER | c.974+6625C>T | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 10/11 | chr17 | 59824398 | |||||||
| chr17:59824466 | G | A | 1 | a0001c0001t0005g0002 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.974+6693G>A | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 10/11 | chr17 | 59824466 | |||||||
| chr17:59824571 | T | TA | 26 | a0001c0001t0001g0089 a0001c0001t0001g0153 a0001c0001t0001g0158 others(23): Show |
26 | HG00140.hp1 HG00423.hp2 HG01109.hp1 others(23): Show |
intron_variant | MODIFIER | c.974+6816dupA | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr17 | 59824571 | ||||||
| chr17:59824581 | A | C | 1 | a0001c0001t0001g0087 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.974+6808A>C | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 10/11 | chr17 | 59824581 | |||||||
| chr17:59824621 | C | A | 1 | a0001c0001t0001g0222 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.974+6848C>A | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 10/11 | chr17 | 59824621 | |||||||
| chr17:59824851 | T | C | 1 | a0001c0001t0001g0187 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.974+7078T>C | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 10/11 | chr17 | 59824851 | |||||||
| chr17:59824852 | G | A | 1 | a0001c0001t0001g0187 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.974+7079G>A | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 10/11 | chr17 | 59824852 | |||||||
| chr17:59824854 | C | T | 1 | a0001c0001t0001g0187 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.974+7081C>T | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 10/11 | chr17 | 59824854 | |||||||
| chr17:59824858 | G | A | 1 | a0001c0001t0001g0187 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.974+7085G>A | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 10/11 | chr17 | 59824858 | |||||||
| chr17:59824862 | G | A | 1 | a0001c0001t0001g0187 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.974+7089G>A | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 10/11 | chr17 | 59824862 | |||||||
| chr17:59824867 | C | T | 1 | a0001c0001t0001g0187 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.974+7094C>T | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 10/11 | chr17 | 59824867 | |||||||
| chr17:59824872 | C | CA | 121 | a0001c0001t0001g0003 a0001c0001t0001g0069 a0001c0001t0001g0070 others(118): Show |
121 | HG00140.hp1 HG00408.hp2 HG00438.hp1 others(118): Show |
intron_variant | MODIFIER | c.974+7121dupA | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr17 | 59824872 | ||||||
| chr17:59824872 | C | CAA | 34 | a0001c0001t0001g0078 a0001c0001t0001g0080 a0001c0001t0001g0278 others(31): Show |
34 | HG00438.hp2 HG00642.hp1 HG00673.hp2 others(31): Show |
intron_variant | MODIFIER | c.974+7120_974+7121d others(4): Show |
VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr17 | 59824872 | ||||||
| chr17:59824901 | A | G | 1 | a0001c0001t0001g0080 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.974+7128A>G | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 10/11 | chr17 | 59824901 | |||||||
| chr17:59824904 | C | A | 1 | a0001c0001t0001g0187 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.974+7131C>A | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 10/11 | chr17 | 59824904 | |||||||
| chr17:59824907 | G | C | 1 | a0001c0001t0001g0187 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.974+7134G>C | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 10/11 | chr17 | 59824907 | |||||||
| chr17:59824908 | G | A | 1 | a0001c0001t0001g0187 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.974+7135G>A | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 10/11 | chr17 | 59824908 | |||||||
| chr17:59824909 | T | C | 1 | a0001c0001t0001g0187 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.974+7136T>C | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 10/11 | chr17 | 59824909 | |||||||
| chr17:59824910 | G | A | 1 | a0001c0001t0001g0187 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.974+7137G>A | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 10/11 | chr17 | 59824910 | |||||||
| chr17:59824911 | G | A | 1 | a0001c0001t0001g0187 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.974+7138G>A | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 10/11 | chr17 | 59824911 | |||||||
| chr17:59824914 | C | A | 1 | a0001c0001t0001g0187 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.974+7141C>A | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 10/11 | chr17 | 59824914 | |||||||
| chr17:59824921 | G | A | 1 | a0001c0001t0001g0187 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.974+7148G>A | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 10/11 | chr17 | 59824921 | |||||||
| chr17:59824926 | C | G | 1 | a0001c0001t0001g0187 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.974+7153C>G | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 10/11 | chr17 | 59824926 | |||||||
| chr17:59824937 | G | T | 1 | a0001c0001t0001g0187 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.974+7164G>T | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 10/11 | chr17 | 59824937 | |||||||
| chr17:59824938 | G | T | 1 | a0001c0001t0001g0187 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.974+7165G>T | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 10/11 | chr17 | 59824938 | |||||||
| chr17:59824942 | G | C | 1 | a0001c0001t0001g0187 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.974+7169G>C | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 10/11 | chr17 | 59824942 | |||||||
| chr17:59824943 | C | T | 1 | a0001c0001t0001g0187 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.974+7170C>T | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 10/11 | chr17 | 59824943 | |||||||
| chr17:59824944 | C | A | 1 | a0001c0001t0001g0187 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.974+7171C>A | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 10/11 | chr17 | 59824944 | |||||||
| chr17:59824947 | G | A | 1 | a0001c0001t0001g0187 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.974+7174G>A | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 10/11 | chr17 | 59824947 | |||||||
| chr17:59824950 | A | T | 1 | a0001c0001t0001g0187 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.974+7177A>T | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 10/11 | chr17 | 59824950 | |||||||
| chr17:59824951 | G | A | 1 | a0001c0001t0001g0187 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.974+7178G>A | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 10/11 | chr17 | 59824951 | |||||||
| chr17:59824952 | A | G | 1 | a0001c0001t0001g0187 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.974+7179A>G | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 10/11 | chr17 | 59824952 | |||||||
| chr17:59824954 | G | T | 1 | a0001c0001t0001g0187 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.974+7181G>T | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 10/11 | chr17 | 59824954 | |||||||
| chr17:59824955 | G | C | 1 | a0001c0001t0001g0187 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.974+7182G>C | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 10/11 | chr17 | 59824955 | |||||||
| chr17:59824956 | A | T | 1 | a0001c0001t0001g0187 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.974+7183A>T | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 10/11 | chr17 | 59824956 | |||||||
| chr17:59824963 | G | C | 1 | a0001c0001t0001g0187 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.974+7190G>C | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 10/11 | chr17 | 59824963 | |||||||
| chr17:59824964 | A | T | 1 | a0001c0001t0001g0187 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.974+7191A>T | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 10/11 | chr17 | 59824964 | |||||||
| chr17:59824969 | T | A | 1 | a0001c0001t0001g0187 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.974+7196T>A | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 10/11 | chr17 | 59824969 | |||||||
| chr17:59824971 | A | C | 1 | a0001c0001t0001g0187 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.974+7198A>C | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 10/11 | chr17 | 59824971 | |||||||
| chr17:59824972 | G | T | 1 | a0001c0001t0001g0187 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.974+7199G>T | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 10/11 | chr17 | 59824972 | |||||||
| chr17:59824975 | A | C | 1 | a0001c0001t0001g0187 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.974+7202A>C | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 10/11 | chr17 | 59824975 | |||||||
| chr17:59824980 | A | G | 1 | a0001c0001t0001g0187 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.974+7207A>G | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 10/11 | chr17 | 59824980 | |||||||
| chr17:59824984 | C | T | 1 | a0001c0001t0001g0187 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.974+7211C>T | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 10/11 | chr17 | 59824984 | |||||||
| chr17:59824985 | A | C | 1 | a0001c0001t0001g0187 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.974+7212A>C | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 10/11 | chr17 | 59824985 | |||||||
| chr17:59824989 | T | A | 1 | a0001c0001t0001g0187 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.974+7216T>A | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 10/11 | chr17 | 59824989 | |||||||
| chr17:59824990 | G | T | 1 | a0001c0001t0001g0187 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.974+7217G>T | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 10/11 | chr17 | 59824990 | |||||||
| chr17:59825000 | A | C | 1 | a0001c0001t0001g0187 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.974+7227A>C | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 10/11 | chr17 | 59825000 | |||||||
| chr17:59825001 | T | A | 1 | a0001c0001t0001g0187 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.974+7228T>A | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 10/11 | chr17 | 59825001 | |||||||
| chr17:59825005 | G | T | 1 | a0001c0001t0001g0187 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.974+7232G>T | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 10/11 | chr17 | 59825005 | |||||||
| chr17:59825006 | A | G | 1 | a0001c0001t0001g0187 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.974+7233A>G | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 10/11 | chr17 | 59825006 | |||||||
| chr17:59825010 | C | T | 1 | a0001c0001t0001g0187 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.974+7237C>T | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 10/11 | chr17 | 59825010 | |||||||
| chr17:59825015 | G | T | 1 | a0001c0001t0001g0187 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.974+7242G>T | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 10/11 | chr17 | 59825015 | |||||||
| chr17:59825018 | A | C | 1 | a0001c0001t0001g0187 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.974+7245A>C | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 10/11 | chr17 | 59825018 | |||||||
| chr17:59825019 | G | T | 1 | a0001c0001t0001g0187 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.974+7246G>T | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 10/11 | chr17 | 59825019 | |||||||
| chr17:59825021 | T | A | 1 | a0001c0001t0001g0187 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.974+7248T>A | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 10/11 | chr17 | 59825021 | |||||||
| chr17:59825025 | A | T | 1 | a0001c0001t0001g0187 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.974+7252A>T | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 10/11 | chr17 | 59825025 | |||||||
| chr17:59825026 | G | C | 1 | a0001c0001t0001g0187 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.974+7253G>C | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 10/11 | chr17 | 59825026 | |||||||
| chr17:59825033 | A | T | 1 | a0001c0001t0001g0187 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.974+7260A>T | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 10/11 | chr17 | 59825033 | |||||||
| chr17:59825034 | G | C | 1 | a0001c0001t0001g0187 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.974+7261G>C | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 10/11 | chr17 | 59825034 | |||||||
| chr17:59825035 | A | C | 1 | a0001c0001t0001g0187 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.974+7262A>C | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 10/11 | chr17 | 59825035 | |||||||
| chr17:59825037 | C | T | 1 | a0001c0001t0001g0187 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.974+7264C>T | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 10/11 | chr17 | 59825037 | |||||||
| chr17:59825038 | T | C | 1 | a0001c0001t0001g0187 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.974+7265T>C | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 10/11 | chr17 | 59825038 | |||||||
| chr17:59825039 | A | T | 1 | a0001c0001t0001g0187 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.974+7266A>T | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 10/11 | chr17 | 59825039 | |||||||
| chr17:59825046 | T | C | 1 | a0001c0001t0001g0187 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.974+7273T>C | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 10/11 | chr17 | 59825046 | |||||||
| chr17:59825049 | T | G | 1 | a0001c0001t0001g0187 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.974+7276T>G | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 10/11 | chr17 | 59825049 | |||||||
| chr17:59825050 | A | G | 1 | a0001c0001t0001g0187 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.974+7277A>G | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 10/11 | chr17 | 59825050 | |||||||
| chr17:59825051 | G | C | 1 | a0001c0001t0001g0187 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.974+7278G>C | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 10/11 | chr17 | 59825051 | |||||||
| chr17:59825055 | A | C | 1 | a0001c0001t0001g0187 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.974+7282A>C | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 10/11 | chr17 | 59825055 | |||||||
| chr17:59825056 | A | C | 1 | a0001c0001t0001g0187 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.974+7283A>C | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 10/11 | chr17 | 59825056 | |||||||
| chr17:59825061 | C | G | 1 | a0001c0001t0001g0187 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.974+7288C>G | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 10/11 | chr17 | 59825061 | |||||||
| chr17:59825066 | T | C | 1 | a0001c0001t0001g0187 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.974+7293T>C | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 10/11 | chr17 | 59825066 | |||||||
| chr17:59825069 | T | G | 1 | a0001c0001t0001g0187 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.974+7296T>G | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 10/11 | chr17 | 59825069 | |||||||
| chr17:59825072 | T | C | 1 | a0001c0001t0001g0187 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.974+7299T>C | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 10/11 | chr17 | 59825072 | |||||||
| chr17:59825073 | T | C | 1 | a0001c0001t0001g0187 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.974+7300T>C | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 10/11 | chr17 | 59825073 | |||||||
| chr17:59825074 | G | A | 1 | a0001c0001t0001g0187 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.974+7301G>A | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 10/11 | chr17 | 59825074 | |||||||
| chr17:59825075 | T | C | 1 | a0001c0001t0001g0187 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.974+7302T>C | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 10/11 | chr17 | 59825075 | |||||||
| chr17:59825076 | G | C | 1 | a0001c0001t0001g0187 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.974+7303G>C | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 10/11 | chr17 | 59825076 | |||||||
| chr17:59825077 | A | AT | 49 | a0001c0001t0001g0078 a0001c0001t0001g0080 a0001c0001t0001g0084 others(46): Show |
49 | HG00438.hp2 HG00621.hp1 HG00673.hp1 others(46): Show |
intron_variant | MODIFIER | c.974+7331dupT | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr17 | 59825077 | ||||||
| chr17:59825077 | AT | A | 33 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0006 others(30): Show |
33 | HG00140.hp1 HG01099.hp1 HG01168.hp2 others(30): Show |
intron_variant | MODIFIER | c.974+7331delT | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr17 | 59825077 | ||||||
| chr17:59825077 | ATT | A | 24 | a0001c0001t0001g0101 a0001c0001t0001g0103 a0001c0001t0001g0158 others(21): Show |
24 | HG00423.hp1 HG00438.hp1 HG00621.hp2 others(21): Show |
intron_variant | MODIFIER | c.974+7330_974+7331d others(4): Show |
VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr17 | 59825077 | ||||||
| chr17:59825077 | ATTT | A | 69 | a0001c0001t0001g0069 a0001c0001t0001g0070 a0001c0001t0001g0095 others(66): Show |
69 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(66): Show |
intron_variant | MODIFIER | c.974+7329_974+7331d others(5): Show |
VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr17 | 59825077 | ||||||
| chr17:59825077 | ATTTT | A | 8 | a0001c0001t0001g0190 a0001c0001t0001g0203 a0001c0001t0001g0212 others(5): Show |
8 | HG01109.hp2 HG01884.hp2 HG02615.hp1 others(5): Show |
intron_variant | MODIFIER | c.974+7328_974+7331d others(6): Show |
VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr17 | 59825077 | ||||||
| chr17:59825079 | T | G | 1 | a0001c0001t0001g0187 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.974+7306T>G | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 10/11 | chr17 | 59825079 | |||||||
| chr17:59825080 | T | C | 1 | a0001c0001t0001g0187 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.974+7307T>C | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 10/11 | chr17 | 59825080 | |||||||
| chr17:59825081 | T | C | 1 | a0001c0001t0001g0187 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.974+7308T>C | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 10/11 | chr17 | 59825081 | |||||||
| chr17:59825110 | A | G | 1 | a0001c0001t0001g0187 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.974+7337A>G | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 10/11 | chr17 | 59825110 | |||||||
| chr17:59825115 | T | C | 1 | a0001c0001t0001g0187 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.974+7342T>C | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 10/11 | chr17 | 59825115 | |||||||
| chr17:59825119 | T | C | 1 | a0001c0001t0001g0187 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.974+7346T>C | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 10/11 | chr17 | 59825119 | |||||||
| chr17:59825123 | A | G | 1 | a0001c0001t0001g0187 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.974+7350A>G | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 10/11 | chr17 | 59825123 | |||||||
| chr17:59825125 | T | C | 1 | a0001c0001t0001g0187 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.974+7352T>C | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 10/11 | chr17 | 59825125 | |||||||
| chr17:59825126 | G | A | 1 | a0001c0001t0001g0187 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.974+7353G>A | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 10/11 | chr17 | 59825126 | |||||||
| chr17:59825139 | C | T | 1 | a0001c0001t0001g0187 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.974+7366C>T | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 10/11 | chr17 | 59825139 | |||||||
| chr17:59825142 | T | A | 1 | a0001c0001t0001g0187 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.974+7369T>A | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 10/11 | chr17 | 59825142 | |||||||
| chr17:59825147 | T | C | 1 | a0001c0001t0001g0187 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.974+7374T>C | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 10/11 | chr17 | 59825147 | |||||||
| chr17:59825157 | A | G | 1 | a0001c0001t0001g0187 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.974+7384A>G | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 10/11 | chr17 | 59825157 | |||||||
| chr17:59825159 | C | T | 1 | a0001c0001t0001g0187 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.974+7386C>T | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 10/11 | chr17 | 59825159 | |||||||
| chr17:59825164 | G | A | 1 | a0001c0001t0001g0187 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.974+7391G>A | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 10/11 | chr17 | 59825164 | |||||||
| chr17:59825181 | T | G | 1 | a0001c0001t0001g0187 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.974+7408T>G | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 10/11 | chr17 | 59825181 | |||||||
| chr17:59825219 | A | T | 2 | a0001c0001t0003g0108 a0001c0001t0003g0133 |
2 | HG02071.hp2 HG03927.hp2 |
intron_variant | MODIFIER | c.974+7446A>T | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 10/11 | chr17 | 59825219 | |||||||
| chr17:59825680 | G | C | 53 | a0001c0001t0003g0105 a0001c0001t0003g0107 a0001c0001t0003g0108 others(50): Show |
53 | HG00438.hp2 HG00642.hp1 HG00673.hp2 others(50): Show |
intron_variant | MODIFIER | c.974+7907G>C | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 10/11 | chr17 | 59825680 | |||||||
| chr17:59825986 | T | A | 1 | a0001c0001t0001g0187 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.974+8213T>A | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 10/11 | chr17 | 59825986 | |||||||
| chr17:59826196 | A | G | 1 | a0001c0001t0001g0095 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.974+8423A>G | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 10/11 | chr17 | 59826196 | |||||||
| chr17:59826595 | G | A | 2 | a0001c0001t0003g0113 a0001c0001t0009g0109 |
2 | HG00642.hp1 HG03831.hp2 |
intron_variant | MODIFIER | c.974+8822G>A | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 10/11 | chr17 | 59826595 | |||||||
| chr17:59826941 | A | C | 4 | a0001c0001t0001g0078 a0001c0001t0001g0079 a0001c0001t0001g0080 others(1): Show |
4 | HG01243.hp1 HG02451.hp2 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.974+9168A>C | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 10/11 | chr17 | 59826941 | |||||||
| chr17:59827383 | C | G | 18 | a0001c0001t0001g0150 a0001c0001t0001g0153 a0001c0001t0001g0158 others(15): Show |
18 | HG00140.hp1 HG01109.hp1 HG01255.hp1 others(15): Show |
intron_variant | MODIFIER | c.974+9610C>G | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 10/11 | chr17 | 59827383 | |||||||
| chr17:59827415 | C | T | 1 | a0001c0001t0004g0267 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.974+9642C>T | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 10/11 | chr17 | 59827415 | |||||||
| chr17:59827462 | A | G | 181 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(178): Show |
181 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(178): Show |
intron_variant | MODIFIER | c.974+9689A>G | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 10/11 | chr17 | 59827462 | |||||||
| chr17:59827831 | G | A | 1 | a0001c0001t0001g0184 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.974+10058G>A | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 10/11 | chr17 | 59827831 | |||||||
| chr17:59827873 | G | T | 21 | a0001c0001t0001g0003 a0001c0001t0001g0076 a0001c0001t0001g0077 others(18): Show |
21 | HG01243.hp1 HG01891.hp2 HG02257.hp1 others(18): Show |
intron_variant | MODIFIER | c.974+10100G>T | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 10/11 | chr17 | 59827873 | |||||||
| chr17:59828024 | TA | T | 7 | a0001c0001t0001g0095 a0001c0001t0001g0160 a0001c0001t0002g0020 others(4): Show |
7 | HG01168.hp1 HG01975.hp2 HG02895.hp1 others(4): Show |
intron_variant | MODIFIER | c.975-10255delA | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr17 | 59828024 | ||||||
| chr17:59828040 | A | G | 1 | a0001c0001t0006g0286 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.975-10255A>G | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 10/11 | chr17 | 59828040 | |||||||
| chr17:59828403 | A | C | 1 | a0001c0001t0002g0093 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.975-9892A>C | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 10/11 | chr17 | 59828403 | |||||||
| chr17:59828927 | C | G | 107 | a0001c0001t0001g0069 a0001c0001t0001g0070 a0001c0001t0001g0100 others(104): Show |
107 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(104): Show |
intron_variant | MODIFIER | c.975-9368C>G | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 10/11 | chr17 | 59828927 | |||||||
| chr17:59828957 | A | C | 89 | a0001c0001t0001g0069 a0001c0001t0001g0070 a0001c0001t0001g0100 others(86): Show |
89 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(86): Show |
intron_variant | MODIFIER | c.975-9338A>C | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 10/11 | chr17 | 59828957 | |||||||
| chr17:59828962 | A | G | 1 | a0001c0001t0002g0051 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.975-9333A>G | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 10/11 | chr17 | 59828962 | |||||||
| chr17:59828967 | C | T | 1 | a0001c0001t0002g0051 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.975-9328C>T | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 10/11 | chr17 | 59828967 | |||||||
| chr17:59829215 | TC | T | 89 | a0001c0001t0001g0069 a0001c0001t0001g0070 a0001c0001t0001g0100 others(86): Show |
89 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(86): Show |
intron_variant | MODIFIER | c.975-9078delC | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr17 | 59829215 | ||||||
| chr17:59829378 | C | T | 1 | a0001c0001t0002g0066 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.975-8917C>T | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 10/11 | chr17 | 59829378 | |||||||
| chr17:59829383 | A | T | 1 | a0001c0001t0001g0187 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.975-8912A>T | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 10/11 | chr17 | 59829383 | |||||||
| chr17:59829502 | C | G | 1 | a0001c0001t0001g0249 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.975-8793C>G | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 10/11 | chr17 | 59829502 | |||||||
| chr17:59829577 | G | A | 3 | a0001c0001t0001g0280 a0001c0001t0008g0279 a0001c0001t0008g0281 |
3 | HG02145.hp2 HG02818.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.975-8718G>A | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 10/11 | chr17 | 59829577 | |||||||
| chr17:59830064 | A | G | 1 | a0001c0001t0001g0139 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.975-8231A>G | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 10/11 | chr17 | 59830064 | |||||||
| chr17:59830407 | T | A | 181 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(178): Show |
181 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(178): Show |
intron_variant | MODIFIER | c.975-7888T>A | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 10/11 | chr17 | 59830407 | |||||||
| chr17:59830428 | T | G | 1 | a0001c0001t0001g0248 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.975-7867T>G | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 10/11 | chr17 | 59830428 | |||||||
| chr17:59830465 | A | C | 1 | a0001c0001t0002g0029 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.975-7830A>C | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 10/11 | chr17 | 59830465 | |||||||
| chr17:59830589 | A | G | 62 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(59): Show |
62 | HG00438.hp2 HG00642.hp1 HG00673.hp2 others(59): Show |
intron_variant | MODIFIER | c.975-7706A>G | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 10/11 | chr17 | 59830589 | |||||||
| chr17:59830598 | T | G | 1 | a0001c0001t0001g0088 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.975-7697T>G | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 10/11 | chr17 | 59830598 | |||||||
| chr17:59830735 | T | C | 62 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(59): Show |
62 | HG00438.hp2 HG00642.hp1 HG00673.hp2 others(59): Show |
intron_variant | MODIFIER | c.975-7560T>C | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 10/11 | chr17 | 59830735 | |||||||
| chr17:59831049 | C | T | 2 | a0001c0001t0003g0136 a0001c0001t0003g0147 |
2 | HG00438.hp2 NA18992.hp2 |
intron_variant | MODIFIER | c.975-7246C>T | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 10/11 | chr17 | 59831049 | |||||||
| chr17:59831094 | C | T | 1 | a0001c0001t0001g0080 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.975-7201C>T | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 10/11 | chr17 | 59831094 | |||||||
| chr17:59831576 | C | T | 2 | a0001c0001t0006g0285 a0001c0001t0006g0286 |
2 | HG02109.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.975-6719C>T | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 10/11 | chr17 | 59831576 | |||||||
| chr17:59831612 | A | AT | 39 | a0001c0001t0001g0003 a0001c0001t0001g0076 a0001c0001t0001g0077 others(36): Show |
39 | HG01243.hp1 HG01361.hp1 HG01891.hp2 others(36): Show |
intron_variant | MODIFIER | c.975-6663dupT | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr17 | 59831612 | ||||||
| chr17:59831612 | A | ATT | 8 | a0001c0001t0001g0082 a0001c0001t0001g0084 a0001c0001t0001g0091 others(5): Show |
8 | HG01109.hp2 HG01891.hp1 HG02559.hp1 others(5): Show |
intron_variant | MODIFIER | c.975-6664_975-6663d others(4): Show |
VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr17 | 59831612 | ||||||
| chr17:59831612 | A | ATTT | 14 | a0001c0001t0001g0150 a0001c0001t0001g0153 a0001c0001t0001g0158 others(11): Show |
14 | HG01109.hp1 HG01255.hp1 HG01256.hp1 others(11): Show |
intron_variant | MODIFIER | c.975-6665_975-6663d others(5): Show |
VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr17 | 59831612 | ||||||
| chr17:59831612 | AT | A | 63 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(60): Show |
63 | HG00438.hp2 HG00642.hp1 HG00673.hp2 others(60): Show |
intron_variant | MODIFIER | c.975-6663delT | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr17 | 59831612 | ||||||
| chr17:59831772 | A | T | 8 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(5): Show |
8 | HG01099.hp1 HG01884.hp1 HG01952.hp2 others(5): Show |
intron_variant | MODIFIER | c.975-6523A>T | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 10/11 | chr17 | 59831772 | |||||||
| chr17:59831801 | G | GTT | 18 | a0001c0001t0001g0153 a0001c0001t0001g0158 a0001c0001t0001g0159 others(15): Show |
18 | HG00140.hp1 HG01109.hp1 HG01255.hp1 others(15): Show |
intron_variant | MODIFIER | c.975-6485_975-6484d others(4): Show |
VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr17 | 59831801 | ||||||
| chr17:59832012 | A | G | 89 | a0001c0001t0001g0069 a0001c0001t0001g0070 a0001c0001t0001g0100 others(86): Show |
89 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(86): Show |
intron_variant | MODIFIER | c.975-6283A>G | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 10/11 | chr17 | 59832012 | |||||||
| chr17:59832068 | A | T | 89 | a0001c0001t0001g0069 a0001c0001t0001g0070 a0001c0001t0001g0100 others(86): Show |
89 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(86): Show |
intron_variant | MODIFIER | c.975-6227A>T | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 10/11 | chr17 | 59832068 | |||||||
| chr17:59832121 | A | G | 1 | a0001c0001t0003g0121 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.975-6174A>G | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 10/11 | chr17 | 59832121 | |||||||
| chr17:59832182 | C | CT | 80 | a0001c0001t0001g0069 a0001c0001t0001g0104 a0001c0001t0001g0153 others(77): Show |
80 | HG00140.hp1 HG00408.hp2 HG00423.hp2 others(77): Show |
intron_variant | MODIFIER | c.975-6089dupT | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr17 | 59832182 | ||||||
| chr17:59832182 | C | CTT | 12 | a0001c0001t0001g0070 a0001c0001t0001g0150 a0001c0001t0001g0161 others(9): Show |
12 | HG00673.hp2 HG01255.hp1 HG01256.hp1 others(9): Show |
intron_variant | MODIFIER | c.975-6090_975-6089d others(4): Show |
VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr17 | 59832182 | ||||||
| chr17:59832182 | C | CTTT | 20 | a0001c0001t0001g0003 a0001c0001t0001g0076 a0001c0001t0001g0077 others(17): Show |
20 | HG01243.hp1 HG01891.hp2 HG02257.hp1 others(17): Show |
intron_variant | MODIFIER | c.975-6091_975-6089d others(5): Show |
VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr17 | 59832182 | ||||||
| chr17:59832182 | CT | C | 14 | a0001c0001t0001g0201 a0001c0001t0001g0204 a0001c0001t0001g0210 others(11): Show |
14 | HG02004.hp2 HG02145.hp2 HG02818.hp1 others(11): Show |
intron_variant | MODIFIER | c.975-6089delT | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr17 | 59832182 | ||||||
| chr17:59832182 | CTTT | C | 8 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(5): Show |
8 | HG01099.hp1 HG01884.hp1 HG01952.hp2 others(5): Show |
intron_variant | MODIFIER | c.975-6091_975-6089d others(5): Show |
VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr17 | 59832182 | ||||||
| chr17:59832348 | A | G | 1 | a0001c0001t0001g0095 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.975-5947A>G | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 10/11 | chr17 | 59832348 | |||||||
| chr17:59832573 | A | ATTTGT | 6 | a0001c0001t0001g0084 a0001c0001t0001g0090 a0001c0001t0003g0108 others(3): Show |
6 | HG02615.hp1 HG02622.hp1 HG02895.hp1 others(3): Show |
intron_variant | MODIFIER | c.975-5687_975-5683d others(7): Show |
VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr17 | 59832573 | ||||||
| chr17:59832573 | A | ATTTGTTT others(3): Show |
46 | a0001c0001t0002g0050 a0001c0001t0003g0110 a0001c0001t0003g0111 others(43): Show |
46 | HG00642.hp1 HG00673.hp2 HG00738.hp2 others(43): Show |
intron_variant | MODIFIER | c.975-5692_975-5683d others(12): Show |
VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr17 | 59832573 | ||||||
| chr17:59832573 | A | ATTTGTTT others(8): Show |
4 | a0001c0001t0001g0277 a0001c0001t0003g0105 a0001c0001t0003g0107 others(1): Show |
4 | HG01261.hp1 HG02647.hp1 HG02723.hp1 others(1): Show |
intron_variant | MODIFIER | c.975-5697_975-5683d others(17): Show |
VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr17 | 59832573 | ||||||
| chr17:59832573 | ATTTGT | A | 119 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(116): Show |
119 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(116): Show |
intron_variant | MODIFIER | c.975-5687_975-5683d others(7): Show |
VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr17 | 59832573 | ||||||
| chr17:59832633 | G | A | 1 | a0001c0001t0001g0081 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.975-5662G>A | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 10/11 | chr17 | 59832633 | |||||||
| chr17:59832761 | A | AT | 106 | a0001c0001t0001g0069 a0001c0001t0001g0070 a0001c0001t0001g0081 others(103): Show |
106 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(103): Show |
intron_variant | MODIFIER | c.975-5513dupT | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr17 | 59832761 | ||||||
| chr17:59832761 | A | ATT | 60 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(57): Show |
60 | HG00438.hp2 HG00642.hp1 HG00738.hp2 others(57): Show |
intron_variant | MODIFIER | c.975-5514_975-5513d others(4): Show |
VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr17 | 59832761 | ||||||
| chr17:59832761 | A | T | 1 | a0001c0001t0003g0115 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.975-5534A>T | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 10/11 | chr17 | 59832761 | |||||||
| chr17:59832763 | T | A | 1 | a0001c0001t0001g0092 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.975-5532T>A | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 10/11 | chr17 | 59832763 | |||||||
| chr17:59832902 | T | C | 119 | a0001c0001t0001g0069 a0001c0001t0001g0070 a0001c0001t0001g0095 others(116): Show |
119 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(116): Show |
intron_variant | MODIFIER | c.975-5393T>C | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 10/11 | chr17 | 59832902 | |||||||
| chr17:59833858 | C | T | 3 | a0001c0001t0003g0131 a0001c0001t0003g0134 a0001c0001t0003g0146 |
3 | HG02895.hp1 HG03579.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.975-4437C>T | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 10/11 | chr17 | 59833858 | |||||||
| chr17:59833869 | A | G | 89 | a0001c0001t0001g0069 a0001c0001t0001g0070 a0001c0001t0001g0100 others(86): Show |
89 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(86): Show |
intron_variant | MODIFIER | c.975-4426A>G | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 10/11 | chr17 | 59833869 | |||||||
| chr17:59834403 | T | C | 1 | a0001c0001t0001g0008 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.975-3892T>C | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 10/11 | chr17 | 59834403 | |||||||
| chr17:59834483 | G | A | 3 | a0001c0001t0001g0222 a0001c0001t0006g0283 a0001c0001t0006g0284 |
3 | HG00280.hp1 HG03130.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.975-3812G>A | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 10/11 | chr17 | 59834483 | |||||||
| chr17:59834626 | A | AT | 104 | a0001c0001t0001g0069 a0001c0001t0001g0070 a0001c0001t0001g0090 others(101): Show |
104 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(101): Show |
intron_variant | MODIFIER | c.975-3653dupT | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr17 | 59834626 | ||||||
| chr17:59834626 | A | ATT | 14 | a0001c0001t0001g0132 a0001c0001t0001g0187 a0001c0001t0001g0210 others(11): Show |
14 | HG01109.hp2 HG02004.hp2 HG02615.hp1 others(11): Show |
intron_variant | MODIFIER | c.975-3654_975-3653d others(4): Show |
VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr17 | 59834626 | ||||||
| chr17:59834978 | T | C | 1 | a0001c0001t0001g0232 | 1 | NA18943.hp2 | intron_variant | MODIFIER | c.975-3317T>C | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 10/11 | chr17 | 59834978 | |||||||
| chr17:59835030 | G | A | 11 | a0001c0001t0004g0262 a0001c0001t0004g0263 a0001c0001t0004g0265 others(8): Show |
11 | HG01109.hp2 HG02615.hp1 HG02896.hp1 others(8): Show |
intron_variant | MODIFIER | c.975-3265G>A | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 10/11 | chr17 | 59835030 | |||||||
| chr17:59835080 | G | A | 1 | a0001c0001t0002g0014 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.975-3215G>A | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 10/11 | chr17 | 59835080 | |||||||
| chr17:59835135 | G | GT | 29 | a0001c0001t0002g0014 a0001c0001t0002g0015 a0001c0001t0002g0031 others(26): Show |
29 | HG00408.hp2 HG00423.hp2 HG00544.hp1 others(26): Show |
intron_variant | MODIFIER | c.975-3149dupT | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr17 | 59835135 | ||||||
| chr17:59835168 | G | A | 1 | a0001c0001t0005g0018 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.975-3127G>A | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 10/11 | chr17 | 59835168 | |||||||
| chr17:59835232 | G | A | 7 | a0001c0001t0001g0201 a0001c0001t0001g0204 a0001c0001t0001g0238 others(4): Show |
7 | HG02145.hp2 HG02818.hp1 HG02886.hp1 others(4): Show |
intron_variant | MODIFIER | c.975-3063G>A | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 10/11 | chr17 | 59835232 | |||||||
| chr17:59835474 | T | C | 1 | a0001c0001t0003g0111 | 1 | HG01071.hp1 | intron_variant | MODIFIER | c.975-2821T>C | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 10/11 | chr17 | 59835474 | |||||||
| chr17:59835493 | G | GT | 18 | a0001c0001t0001g0132 a0001c0001t0001g0191 a0001c0001t0001g0239 others(15): Show |
18 | HG00673.hp2 HG01109.hp2 HG02615.hp1 others(15): Show |
intron_variant | MODIFIER | c.975-2788dupT | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr17 | 59835493 | ||||||
| chr17:59835493 | G | T | 7 | a0001c0001t0001g0201 a0001c0001t0001g0204 a0001c0001t0001g0238 others(4): Show |
7 | HG02145.hp2 HG02818.hp1 HG02886.hp1 others(4): Show |
intron_variant | MODIFIER | c.975-2802G>T | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 10/11 | chr17 | 59835493 | |||||||
| chr17:59835560 | G | A | 1 | a0001c0001t0003g0145 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.975-2735G>A | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 10/11 | chr17 | 59835560 | |||||||
| chr17:59835742 | G | A | 1 | a0001c0001t0004g0270 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.975-2553G>A | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 10/11 | chr17 | 59835742 | |||||||
| chr17:59835928 | T | G | 18 | a0001c0001t0001g0150 a0001c0001t0001g0153 a0001c0001t0001g0158 others(15): Show |
18 | HG00140.hp1 HG01109.hp1 HG01255.hp1 others(15): Show |
intron_variant | MODIFIER | c.975-2367T>G | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 10/11 | chr17 | 59835928 | |||||||
| chr17:59836012 | T | C | 1 | a0001c0001t0001g0095 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.975-2283T>C | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 10/11 | chr17 | 59836012 | |||||||
| chr17:59836196 | G | T | 3 | a0001c0001t0001g0165 a0001c0001t0001g0171 a0001c0001t0001g0172 |
3 | HG01891.hp1 HG02559.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.975-2099G>T | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 10/11 | chr17 | 59836196 | |||||||
| chr17:59836245 | T | A | 9 | a0001c0001t0004g0262 a0001c0001t0004g0263 a0001c0001t0004g0265 others(6): Show |
9 | HG01109.hp2 HG02896.hp1 HG02970.hp1 others(6): Show |
intron_variant | MODIFIER | c.975-2050T>A | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 10/11 | chr17 | 59836245 | |||||||
| chr17:59836268 | C | T | 1 | a0001c0001t0003g0148 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.975-2027C>T | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 10/11 | chr17 | 59836268 | |||||||
| chr17:59836288 | G | T | 1 | a0001c0001t0001g0201 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.975-2007G>T | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 10/11 | chr17 | 59836288 | |||||||
| chr17:59836290 | C | T | 2 | a0001c0001t0001g0171 a0001c0001t0001g0172 |
2 | HG01891.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.975-2005C>T | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 10/11 | chr17 | 59836290 | |||||||
| chr17:59836488 | A | G | 177 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0005 others(174): Show |
177 | HG00408.hp2 HG00423.hp2 HG00438.hp2 others(174): Show |
intron_variant | MODIFIER | c.975-1807A>G | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 10/11 | chr17 | 59836488 | |||||||
| chr17:59836592 | T | C | 2 | a0001c0001t0003g0105 a0001c0001t0003g0148 |
2 | HG02257.hp2 HG02647.hp1 |
intron_variant | MODIFIER | c.975-1703T>C | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 10/11 | chr17 | 59836592 | |||||||
| chr17:59836646 | C | T | 11 | a0001c0001t0004g0262 a0001c0001t0004g0263 a0001c0001t0004g0265 others(8): Show |
11 | HG01109.hp2 HG02615.hp1 HG02896.hp1 others(8): Show |
intron_variant | MODIFIER | c.975-1649C>T | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 10/11 | chr17 | 59836646 | |||||||
| chr17:59836719 | G | GT | 125 | a0001c0001t0001g0003 a0001c0001t0001g0076 a0001c0001t0001g0077 others(122): Show |
125 | HG00140.hp1 HG00408.hp2 HG00423.hp2 others(122): Show |
intron_variant | MODIFIER | c.975-1562dupT | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr17 | 59836719 | ||||||
| chr17:59836719 | GT | G | 10 | a0001c0001t0003g0146 a0001c0001t0004g0265 a0001c0001t0004g0266 others(7): Show |
10 | HG02615.hp1 HG02895.hp1 HG02896.hp1 others(7): Show |
intron_variant | MODIFIER | c.975-1562delT | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr17 | 59836719 | ||||||
| chr17:59836960 | G | T | 18 | a0001c0001t0001g0150 a0001c0001t0001g0153 a0001c0001t0001g0158 others(15): Show |
18 | HG00140.hp1 HG01109.hp1 HG01255.hp1 others(15): Show |
intron_variant | MODIFIER | c.975-1335G>T | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 10/11 | chr17 | 59836960 | |||||||
| chr17:59837020 | T | C | 2 | a0001c0001t0001g0100 a0001c0001t0001g0101 |
2 | HG01358.hp2 NA20752.hp1 |
intron_variant | MODIFIER | c.975-1275T>C | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 10/11 | chr17 | 59837020 | |||||||
| chr17:59837195 | T | A | 1 | a0001c0001t0001g0095 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.975-1100T>A | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 10/11 | chr17 | 59837195 | |||||||
| chr17:59837233 | G | T | 11 | a0001c0001t0004g0262 a0001c0001t0004g0263 a0001c0001t0004g0265 others(8): Show |
11 | HG01109.hp2 HG02615.hp1 HG02896.hp1 others(8): Show |
intron_variant | MODIFIER | c.975-1062G>T | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 10/11 | chr17 | 59837233 | |||||||
| chr17:59837366 | G | T | 1 | a0001c0001t0001g0211 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.975-929G>T | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 10/11 | chr17 | 59837366 | |||||||
| chr17:59837402 | C | T | 1 | a0001c0001t0003g0148 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.975-893C>T | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 10/11 | chr17 | 59837402 | |||||||
| chr17:59837522 | G | A | 1 | a0001c0001t0001g0241 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.975-773G>A | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 10/11 | chr17 | 59837522 | |||||||
| chr17:59837908 | G | T | 1 | a0001c0001t0001g0210 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.975-387G>T | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 10/11 | chr17 | 59837908 | |||||||
| chr17:59838063 | T | G | 5 | a0001c0001t0001g0153 a0001c0001t0001g0168 a0001c0001t0001g0169 others(2): Show |
5 | HG00140.hp1 HG01109.hp1 HG03041.hp1 others(2): Show |
intron_variant | MODIFIER | c.975-232T>G | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 10/11 | chr17 | 59838063 | |||||||
| chr17:59838100 | C | CT | 31 | a0001c0001t0001g0150 a0001c0001t0001g0158 a0001c0001t0001g0159 others(28): Show |
31 | HG00140.hp1 HG00438.hp2 HG00544.hp2 others(28): Show |
intron_variant | MODIFIER | c.975-174dupT | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr17 | 59838100 | ||||||
| chr17:59838100 | CT | C | 34 | a0001c0001t0001g0188 a0001c0001t0001g0203 a0001c0001t0001g0223 others(31): Show |
34 | HG00639.hp2 HG00642.hp1 HG00673.hp2 others(31): Show |
intron_variant | MODIFIER | c.975-174delT | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr17 | 59838100 | ||||||
| chr17:59838100 | CTT | C | 21 | a0001c0001t0001g0003 a0001c0001t0001g0076 a0001c0001t0001g0077 others(18): Show |
21 | HG01243.hp1 HG01891.hp2 HG02257.hp1 others(18): Show |
intron_variant | MODIFIER | c.975-175_975-174del others(2): Show |
VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr17 | 59838100 | ||||||
| chr17:59838104 | T | C | 1 | a0001c0001t0003g0137 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.975-191T>C | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 10/11 | chr17 | 59838104 | |||||||
| chr17:59838105 | T | C | 1 | a0001c0001t0001g0277 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.975-190T>C | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 10/11 | chr17 | 59838105 | |||||||
| chr17:59838461 | C | A | 1 | a0001c0001t0002g0067 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.1077+64C>A | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 11/11 | chr17 | 59838461 | |||||||
| chr17:59838652 | G | T | 1 | a0001c0001t0001g0089 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.1077+255G>T | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 11/11 | chr17 | 59838652 | |||||||
| chr17:59838804 | G | A | 2 | a0001c0001t0001g0188 a0001c0001t0001g0230 |
2 | HG01074.hp2 HG02280.hp1 |
intron_variant | MODIFIER | c.1077+407G>A | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 11/11 | chr17 | 59838804 | |||||||
| chr17:59838871 | T | C | 2 | a0001c0001t0007g0274 a0001c0001t0007g0275 |
2 | HG03491.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.1077+474T>C | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 11/11 | chr17 | 59838871 | |||||||
| chr17:59839182 | C | T | 1 | a0001c0001t0002g0023 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.1078-586C>T | VMP1 | ENSG00000062716.13 | transcript | ENST00000262291.9 | protein_coding | 11/11 | chr17 | 59839182 |