Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 51144 |
| ensemblid | ENSG00000149084.13 |
| hgncid | 18646 |
| symbol | HSD17B12 |
| name | hydroxysteroid 17-beta dehydrogenase 12 |
| refseq_nuc | NM_016142.3 |
| refseq_prot | NP_057226.1 |
| ensembl_nuc | ENST00000278353.10 |
| ensembl_prot | ENSP00000278353.4 |
| mane_status | MANE Select |
| chr | chr11 |
| start | 43680738 |
| end | 43856615 |
| strand | + |
| ver | v1.2 |
| region | chr11:43680738-43856615 |
| region5000 | chr11:43675738-43861615 |
| regionname0 | HSD17B12_chr11_43680738_43856615 |
| regionname5000 | HSD17B12_chr11_43675738_43861615 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/0 | 312 | 176 | 49 | 30 | 58 | 11 | 27 | 45 | HSD17B12_chr11_43675738_43861615 | HSD17B12 | MESAL others(307): Show |
chr11 | 43675738 | 43861615 |
| a0002 | 0/1 | 312 | 98 | 34 | 24 | 27 | 5 | 7 | 19 | HSD17B12_chr11_43675738_43861615 | HSD17B12 | MESAL others(307): Show |
chr11 | 43675738 | 43861615 |
| a0003 | 0/0 | 312 | 3 | 3 | 0 | 0 | 0 | 0 | 0 | HSD17B12_chr11_43675738_43861615 | HSD17B12 | MESAL others(307): Show |
chr11 | 43675738 | 43861615 |
| a0004 | 0/0 | 312 | 2 | 0 | 2 | 0 | 0 | 0 | 0 | HSD17B12_chr11_43675738_43861615 | HSD17B12 | MESAL others(307): Show |
chr11 | 43675738 | 43861615 |
| a0005 | 0/0 | 312 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | HSD17B12_chr11_43675738_43861615 | HSD17B12 | MESAL others(307): Show |
chr11 | 43675738 | 43861615 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/0 | 936 | 151 | 45 | 20 | 58 | 8 | 19 | HSD17B12_chr11_43675738_43861615 | HSD17B12 | ATGGA others(931): Show |
chr11 | 43675738 | 43861615 | ||
| a0001c0003 | 0/0 | 936 | 24 | 3 | 10 | 0 | 3 | 8 | HSD17B12_chr11_43675738_43861615 | HSD17B12 | ATGGA others(931): Show |
chr11 | 43675738 | 43861615 | ||
| a0001c0007 | 0/0 | 936 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B12_chr11_43675738_43861615 | HSD17B12 | ATGGA others(931): Show |
chr11 | 43675738 | 43861615 | ||
| a0002c0002 | 0/1 | 936 | 98 | 34 | 24 | 27 | 5 | 7 | HSD17B12_chr11_43675738_43861615 | HSD17B12 | ATGGA others(931): Show |
chr11 | 43675738 | 43861615 | ||
| a0003c0004 | 0/0 | 936 | 3 | 3 | 0 | 0 | 0 | 0 | HSD17B12_chr11_43675738_43861615 | HSD17B12 | ATGGA others(931): Show |
chr11 | 43675738 | 43861615 | ||
| a0004c0005 | 0/0 | 936 | 2 | 0 | 2 | 0 | 0 | 0 | HSD17B12_chr11_43675738_43861615 | HSD17B12 | ATGGA others(931): Show |
chr11 | 43675738 | 43861615 | ||
| a0005c0006 | 0/0 | 936 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B12_chr11_43675738_43861615 | HSD17B12 | ATGGA others(931): Show |
chr11 | 43675738 | 43861615 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 1/0 | 2396 | 133 | 40 | 20 | 46 | 7 | 19 | HSD17B12_chr11_43675738_43861615 | HSD17B12 | GTCAT others(2391): Show |
chr11 | 43675738 | 43861615 |
| a0001c0001t0003 | 0/0 | 2396 | 17 | 4 | 0 | 12 | 1 | 0 | HSD17B12_chr11_43675738_43861615 | HSD17B12 | GTCAT others(2391): Show |
chr11 | 43675738 | 43861615 |
| a0001c0001t0011 | 0/0 | 2396 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B12_chr11_43675738_43861615 | HSD17B12 | GTCAT others(2391): Show |
chr11 | 43675738 | 43861615 |
| a0001c0003t0001 | 0/0 | 2396 | 15 | 1 | 7 | 0 | 2 | 5 | HSD17B12_chr11_43675738_43861615 | HSD17B12 | GTCAT others(2391): Show |
chr11 | 43675738 | 43861615 |
| a0001c0003t0003 | 0/0 | 2396 | 9 | 2 | 3 | 0 | 1 | 3 | HSD17B12_chr11_43675738_43861615 | HSD17B12 | GTCAT others(2391): Show |
chr11 | 43675738 | 43861615 |
| a0001c0007t0001 | 0/0 | 2396 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B12_chr11_43675738_43861615 | HSD17B12 | GTCAT others(2391): Show |
chr11 | 43675738 | 43861615 |
| a0002c0002t0002 | 0/1 | 2706 | 90 | 29 | 22 | 27 | 5 | 6 | HSD17B12_chr11_43675738_43861615 | HSD17B12 | GTCAT others(2701): Show |
chr11 | 43675738 | 43861615 |
| a0002c0002t0004 | 0/0 | 2712 | 2 | 2 | 0 | 0 | 0 | 0 | HSD17B12_chr11_43675738_43861615 | HSD17B12 | GTCAT others(2707): Show |
chr11 | 43675738 | 43861615 |
| a0002c0002t0005 | 0/0 | 2706 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B12_chr11_43675738_43861615 | HSD17B12 | GTCAT others(2701): Show |
chr11 | 43675738 | 43861615 |
| a0002c0002t0006 | 0/0 | 2706 | 1 | 0 | 1 | 0 | 0 | 0 | HSD17B12_chr11_43675738_43861615 | HSD17B12 | GTCAT others(2701): Show |
chr11 | 43675738 | 43861615 |
| a0002c0002t0007 | 0/0 | 2706 | 1 | 0 | 1 | 0 | 0 | 0 | HSD17B12_chr11_43675738_43861615 | HSD17B12 | GTCAT others(2701): Show |
chr11 | 43675738 | 43861615 |
| a0002c0002t0008 | 0/0 | 2712 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B12_chr11_43675738_43861615 | HSD17B12 | GTCAT others(2707): Show |
chr11 | 43675738 | 43861615 |
| a0002c0002t0009 | 0/0 | 2712 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B12_chr11_43675738_43861615 | HSD17B12 | GTCAT others(2707): Show |
chr11 | 43675738 | 43861615 |
| a0002c0002t0010 | 0/0 | 2706 | 1 | 0 | 0 | 0 | 0 | 1 | HSD17B12_chr11_43675738_43861615 | HSD17B12 | GTCAT others(2701): Show |
chr11 | 43675738 | 43861615 |
| a0003c0004t0001 | 0/0 | 2396 | 3 | 3 | 0 | 0 | 0 | 0 | HSD17B12_chr11_43675738_43861615 | HSD17B12 | GTCAT others(2391): Show |
chr11 | 43675738 | 43861615 |
| a0004c0005t0002 | 0/0 | 2706 | 2 | 0 | 2 | 0 | 0 | 0 | HSD17B12_chr11_43675738_43861615 | HSD17B12 | GTCAT others(2701): Show |
chr11 | 43675738 | 43861615 |
| a0005c0006t0012 | 0/0 | 2396 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B12_chr11_43675738_43861615 | HSD17B12 | GTCAT others(2391): Show |
chr11 | 43675738 | 43861615 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0002 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| a0001c0001t0001g0005 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| a0001c0001t0001g0006 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| a0001c0001t0001g0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| a0001c0001t0001g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| a0001c0001t0001g0009 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| a0001c0001t0001g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| a0001c0001t0001g0026 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| a0001c0001t0001g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| a0001c0001t0001g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| a0001c0001t0001g0030 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| a0001c0001t0001g0031 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| a0001c0001t0001g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| a0001c0001t0001g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| a0001c0001t0001g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| a0001c0001t0001g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| a0001c0001t0001g0036 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| a0001c0001t0001g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| a0001c0001t0001g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| a0001c0001t0001g0042 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| a0001c0001t0001g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| a0001c0001t0001g0044 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| a0001c0001t0001g0045 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| a0001c0001t0001g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| a0001c0001t0001g0047 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| a0001c0001t0001g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| a0001c0001t0001g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| a0001c0001t0001g0051 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| a0001c0001t0001g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| a0001c0001t0001g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| a0001c0001t0001g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| a0001c0001t0001g0055 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| a0001c0001t0001g0056 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| a0001c0001t0001g0057 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| a0001c0001t0001g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| a0001c0001t0001g0059 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| a0001c0001t0001g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| a0001c0001t0001g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| a0001c0001t0001g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| a0001c0001t0001g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| a0001c0001t0001g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| a0001c0001t0001g0068 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| a0001c0001t0001g0069 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| a0001c0001t0001g0070 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| a0001c0001t0001g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| a0001c0001t0001g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| a0001c0001t0001g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| a0001c0001t0001g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| a0001c0001t0001g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| a0001c0001t0001g0077 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| a0001c0001t0001g0078 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| a0001c0001t0001g0079 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| a0001c0001t0001g0080 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| a0001c0001t0001g0081 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| a0001c0001t0001g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| a0001c0001t0001g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| a0001c0001t0001g0084 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| a0001c0001t0001g0085 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| a0001c0001t0001g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| a0001c0001t0001g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| a0001c0001t0001g0088 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| a0001c0001t0001g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| a0001c0001t0001g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| a0001c0001t0001g0091 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| a0001c0001t0001g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| a0001c0001t0001g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| a0001c0001t0001g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| a0001c0001t0001g0095 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| a0001c0001t0001g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| a0001c0001t0001g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| a0001c0001t0001g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| a0001c0001t0001g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| a0001c0001t0001g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| a0001c0001t0001g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| a0001c0001t0001g0102 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| a0001c0001t0001g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| a0001c0001t0001g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| a0001c0001t0001g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| a0001c0001t0001g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| a0001c0001t0001g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| a0001c0001t0001g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| a0001c0001t0001g0113 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| a0001c0001t0001g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| a0001c0001t0001g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| a0001c0001t0001g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| a0001c0001t0001g0121 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| a0001c0001t0001g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| a0001c0001t0001g0123 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| a0001c0001t0001g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| a0001c0001t0001g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| a0001c0001t0001g0128 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| a0001c0001t0001g0129 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| a0001c0001t0001g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| a0001c0001t0001g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| a0001c0001t0001g0195 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| a0001c0001t0001g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| a0001c0001t0001g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| a0001c0001t0001g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| a0001c0001t0001g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| a0001c0001t0001g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| a0001c0001t0001g0208 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| a0001c0001t0001g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| a0001c0001t0001g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| a0001c0001t0001g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| a0001c0001t0001g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| a0001c0001t0001g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| a0001c0001t0001g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| a0001c0001t0001g0215 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| a0001c0001t0001g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| a0001c0001t0001g0217 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| a0001c0001t0001g0218 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| a0001c0001t0001g0219 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| a0001c0001t0001g0220 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| a0001c0001t0001g0221 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| a0001c0001t0001g0222 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| a0001c0001t0001g0223 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| a0001c0001t0001g0224 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| a0001c0001t0001g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| a0001c0001t0001g0254 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| a0001c0001t0001g0255 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| a0001c0001t0001g0256 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| a0001c0001t0001g0257 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| a0001c0001t0001g0258 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| a0001c0001t0001g0259 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| a0001c0001t0001g0260 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| a0001c0001t0001g0262 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| a0001c0001t0001g0263 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| a0001c0001t0001g0265 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| a0001c0001t0001g0266 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| a0001c0001t0001g0270 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| a0001c0001t0001g0271 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| a0001c0001t0001g0276 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| a0001c0001t0003g0013 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| a0001c0001t0003g0014 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| a0001c0001t0003g0015 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| a0001c0001t0003g0016 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| a0001c0001t0003g0017 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| a0001c0001t0003g0018 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| a0001c0001t0003g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| a0001c0001t0003g0020 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| a0001c0001t0003g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| a0001c0001t0003g0023 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| a0001c0001t0003g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| a0001c0001t0003g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| a0001c0001t0003g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| a0001c0001t0003g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| a0001c0001t0003g0267 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| a0001c0001t0003g0268 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| a0001c0001t0003g0278 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| a0001c0001t0011g0269 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| a0001c0003t0001g0197 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| a0001c0003t0001g0198 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| a0001c0003t0001g0225 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| a0001c0003t0001g0227 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| a0001c0003t0001g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| a0001c0003t0001g0233 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| a0001c0003t0001g0234 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| a0001c0003t0001g0235 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| a0001c0003t0001g0236 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| a0001c0003t0001g0237 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| a0001c0003t0001g0238 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| a0001c0003t0001g0239 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| a0001c0003t0001g0240 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| a0001c0003t0001g0272 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| a0001c0003t0001g0273 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| a0001c0003t0003g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| a0001c0003t0003g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| a0001c0003t0003g0242 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| a0001c0003t0003g0243 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| a0001c0003t0003g0244 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| a0001c0003t0003g0245 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| a0001c0003t0003g0246 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| a0001c0003t0003g0247 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| a0001c0003t0003g0248 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| a0001c0007t0001g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| a0002c0002t0002g0001 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| a0002c0002t0002g0004 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| a0002c0002t0002g0025 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| a0002c0002t0002g0027 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| a0002c0002t0002g0037 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| a0002c0002t0002g0038 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| a0002c0002t0002g0039 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| a0002c0002t0002g0049 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| a0002c0002t0002g0064 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| a0002c0002t0002g0066 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| a0002c0002t0002g0072 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| a0002c0002t0002g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| a0002c0002t0002g0110 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| a0002c0002t0002g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| a0002c0002t0002g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| a0002c0002t0002g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| a0002c0002t0002g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| a0002c0002t0002g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| a0002c0002t0002g0127 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| a0002c0002t0002g0130 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| a0002c0002t0002g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| a0002c0002t0002g0132 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| a0002c0002t0002g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| a0002c0002t0002g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| a0002c0002t0002g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| a0002c0002t0002g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| a0002c0002t0002g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| a0002c0002t0002g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| a0002c0002t0002g0139 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| a0002c0002t0002g0140 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| a0002c0002t0002g0141 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| a0002c0002t0002g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| a0002c0002t0002g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| a0002c0002t0002g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| a0002c0002t0002g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| a0002c0002t0002g0147 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| a0002c0002t0002g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| a0002c0002t0002g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| a0002c0002t0002g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| a0002c0002t0002g0151 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| a0002c0002t0002g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| a0002c0002t0002g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| a0002c0002t0002g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| a0002c0002t0002g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| a0002c0002t0002g0158 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| a0002c0002t0002g0159 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| a0002c0002t0002g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| a0002c0002t0002g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| a0002c0002t0002g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| a0002c0002t0002g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| a0002c0002t0002g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| a0002c0002t0002g0165 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| a0002c0002t0002g0166 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| a0002c0002t0002g0167 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| a0002c0002t0002g0168 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| a0002c0002t0002g0169 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| a0002c0002t0002g0170 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| a0002c0002t0002g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| a0002c0002t0002g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| a0002c0002t0002g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| a0002c0002t0002g0174 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| a0002c0002t0002g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| a0002c0002t0002g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| a0002c0002t0002g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| a0002c0002t0002g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| a0002c0002t0002g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| a0002c0002t0002g0180 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| a0002c0002t0002g0181 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| a0002c0002t0002g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| a0002c0002t0002g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| a0002c0002t0002g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| a0002c0002t0002g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| a0002c0002t0002g0187 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| a0002c0002t0002g0188 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| a0002c0002t0002g0189 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| a0002c0002t0002g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| a0002c0002t0002g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| a0002c0002t0002g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| a0002c0002t0002g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| a0002c0002t0002g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| a0002c0002t0002g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| a0002c0002t0002g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| a0002c0002t0002g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| a0002c0002t0002g0251 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| a0002c0002t0002g0252 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| a0002c0002t0002g0253 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| a0002c0002t0002g0261 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| a0002c0002t0002g0275 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| a0002c0002t0002g0277 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| a0002c0002t0004g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| a0002c0002t0004g0274 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| a0002c0002t0005g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| a0002c0002t0006g0108 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| a0002c0002t0007g0146 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| a0002c0002t0008g0003 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| a0002c0002t0009g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| a0002c0002t0010g0157 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| a0003c0004t0001g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| a0003c0004t0001g0249 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| a0003c0004t0001g0264 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| a0004c0005t0002g0011 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| a0004c0005t0002g0012 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| a0005c0006t0012g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0001 | g0195 | EUR | GBR | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| HG00099 | hp2 | a0001 | c0001 | t0001 | g0218 | EUR | GBR | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| HG00140 | hp1 | a0001 | c0003 | t0001 | g0272 | EUR | GBR | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| HG00140 | hp2 | a0002 | c0002 | t0002 | g0187 | EUR | GBR | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| HG00280 | hp1 | a0001 | c0001 | t0003 | g0023 | EUR | FIN | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| HG00280 | hp2 | a0002 | c0002 | t0002 | g0167 | EUR | FIN | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| HG00323 | hp1 | a0002 | c0002 | t0002 | g0165 | EUR | FIN | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| HG00323 | hp2 | a0001 | c0001 | t0001 | g0055 | EUR | FIN | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| HG00408 | hp1 | a0001 | c0001 | t0001 | g0099 | EAS | CHS | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| HG00408 | hp2 | a0002 | c0002 | t0002 | g0118 | EAS | CHS | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| HG00423 | hp1 | a0002 | c0002 | t0002 | g0109 | EAS | CHS | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| HG00423 | hp2 | a0001 | c0001 | t0001 | g0097 | EAS | CHS | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| HG00609 | hp1 | a0002 | c0002 | t0002 | g0150 | EAS | CHS | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| HG00609 | hp2 | a0005 | c0006 | t0012 | g0021 | EAS | CHS | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| HG00639 | hp1 | a0002 | c0002 | t0002 | g0139 | AMR | PUR | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| HG00639 | hp2 | a0001 | c0003 | t0001 | g0234 | AMR | PUR | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| HG00642 | hp1 | a0002 | c0002 | t0002 | g0025 | AMR | PUR | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| HG00642 | hp2 | a0001 | c0003 | t0001 | g0273 | AMR | PUR | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| HG00735 | hp1 | a0002 | c0002 | t0006 | g0108 | AMR | PUR | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| HG00735 | hp2 | a0001 | c0001 | t0001 | g0042 | AMR | PUR | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| HG00738 | hp1 | a0002 | c0002 | t0002 | g0170 | AMR | PUR | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| HG00738 | hp2 | a0001 | c0001 | t0001 | g0091 | AMR | PUR | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| HG01069 | hp1 | a0001 | c0003 | t0001 | g0235 | AMR | PUR | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| HG01069 | hp2 | a0002 | c0002 | t0002 | g0001 | AMR | PUR | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| HG01070 | hp1 | a0002 | c0002 | t0002 | g0127 | AMR | PUR | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| HG01070 | hp2 | a0001 | c0003 | t0003 | g0247 | AMR | PUR | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| HG01071 | hp1 | a0001 | c0003 | t0003 | g0248 | AMR | PUR | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| HG01071 | hp2 | a0002 | c0002 | t0002 | g0001 | AMR | PUR | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| HG01099 | hp1 | a0002 | c0002 | t0002 | g0174 | AMR | PUR | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| HG01099 | hp2 | a0004 | c0005 | t0002 | g0012 | AMR | PUR | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| HG01106 | hp1 | a0001 | c0003 | t0001 | g0236 | AMR | PUR | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| HG01106 | hp2 | a0004 | c0005 | t0002 | g0011 | AMR | PUR | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| HG01109 | hp1 | a0001 | c0001 | t0001 | g0123 | AMR | PUR | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| HG01109 | hp2 | a0002 | c0002 | t0007 | g0146 | AMR | PUR | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| HG01167 | hp1 | a0002 | c0002 | t0002 | g0188 | AMR | PUR | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| HG01167 | hp2 | a0001 | c0003 | t0001 | g0225 | AMR | PUR | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| HG01168 | hp1 | a0001 | c0001 | t0001 | g0031 | AMR | PUR | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| HG01168 | hp2 | a0001 | c0001 | t0001 | g0220 | AMR | PUR | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| HG01175 | hp1 | a0001 | c0001 | t0001 | g0085 | AMR | PUR | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| HG01175 | hp2 | a0002 | c0002 | t0002 | g0132 | AMR | PUR | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| HG01192 | hp1 | a0001 | c0001 | t0001 | g0065 | AMR | PUR | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| HG01192 | hp2 | a0002 | c0002 | t0002 | g0064 | AMR | PUR | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| HG01258 | hp1 | a0002 | c0002 | t0002 | g0180 | AMR | CLM | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| HG01258 | hp2 | a0001 | c0001 | t0001 | g0030 | AMR | CLM | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| HG01261 | hp1 | a0001 | c0001 | t0001 | g0217 | AMR | CLM | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| HG01261 | hp2 | a0001 | c0001 | t0001 | g0009 | AMR | CLM | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| HG01346 | hp1 | a0002 | c0002 | t0002 | g0189 | AMR | CLM | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| HG01346 | hp2 | a0002 | c0002 | t0002 | g0168 | AMR | CLM | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| HG01358 | hp1 | a0002 | c0002 | t0002 | g0159 | AMR | CLM | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| HG01358 | hp2 | a0002 | c0002 | t0002 | g0169 | AMR | CLM | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| HG01361 | hp1 | a0001 | c0001 | t0001 | g0047 | AMR | CLM | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| HG01361 | hp2 | a0001 | c0003 | t0001 | g0237 | AMR | CLM | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| HG01496 | hp1 | a0001 | c0001 | t0001 | g0121 | AMR | CLM | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| HG01496 | hp2 | a0002 | c0002 | t0002 | g0038 | AMR | CLM | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| HG01515 | hp1 | a0001 | c0001 | t0001 | g0077 | EUR | IBS | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| HG01515 | hp2 | a0002 | c0002 | t0002 | g0140 | EUR | IBS | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| HG01516 | hp1 | a0002 | c0002 | t0002 | g0147 | EUR | IBS | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| HG01516 | hp2 | a0001 | c0001 | t0001 | g0044 | EUR | IBS | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| HG01884 | hp1 | a0002 | c0002 | t0002 | g0155 | AFR | ACB | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| HG01884 | hp2 | a0001 | c0001 | t0001 | g0125 | AFR | ACB | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| HG01891 | hp1 | a0002 | c0002 | t0002 | g0253 | AFR | ACB | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| HG01891 | hp2 | a0001 | c0001 | t0001 | g0186 | AFR | ACB | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| HG01928 | hp1 | a0001 | c0001 | t0001 | g0069 | AMR | PEL | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| HG01928 | hp2 | a0001 | c0001 | t0001 | g0215 | AMR | PEL | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| HG01934 | hp1 | a0001 | c0001 | t0001 | g0068 | AMR | PEL | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| HG01934 | hp2 | a0002 | c0002 | t0002 | g0049 | AMR | PEL | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| HG01975 | hp1 | a0002 | c0002 | t0002 | g0072 | AMR | PEL | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| HG01975 | hp2 | a0001 | c0001 | t0001 | g0073 | AMR | PEL | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| HG01978 | hp1 | a0001 | c0003 | t0001 | g0233 | AMR | PEL | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| HG01978 | hp2 | a0002 | c0002 | t0002 | g0066 | AMR | PEL | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| HG02004 | hp1 | a0001 | c0003 | t0003 | g0244 | AMR | PEL | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| HG02004 | hp2 | a0001 | c0001 | t0001 | g0051 | AMR | PEL | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| HG02055 | hp1 | a0001 | c0001 | t0001 | g0111 | AFR | ACB | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| HG02055 | hp2 | a0001 | c0001 | t0001 | g0052 | AFR | ACB | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| HG02080 | hp1 | a0001 | c0001 | t0001 | g0046 | EAS | KHV | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| HG02080 | hp2 | a0002 | c0002 | t0002 | g0183 | EAS | KHV | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| HG02083 | hp1 | a0002 | c0002 | t0002 | g0164 | EAS | KHV | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| HG02083 | hp2 | a0001 | c0001 | t0001 | g0114 | EAS | KHV | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| HG02135 | hp1 | a0002 | c0002 | t0002 | g0119 | EAS | KHV | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| HG02135 | hp2 | a0001 | c0001 | t0001 | g0029 | EAS | KHV | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| HG02155 | hp1 | a0001 | c0001 | t0001 | g0028 | EAS | CDX | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| HG02155 | hp2 | a0002 | c0002 | t0002 | g0160 | EAS | CDX | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| HG02165 | hp1 | a0002 | c0002 | t0002 | g0163 | EAS | CDX | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| HG02165 | hp2 | a0001 | c0001 | t0001 | g0086 | EAS | CDX | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| HG02257 | hp1 | a0001 | c0001 | t0001 | g0010 | AFR | ACB | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| HG02257 | hp2 | a0002 | c0002 | t0002 | g0138 | AFR | ACB | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| HG02258 | hp1 | a0001 | c0007 | t0001 | g0230 | AFR | ACB | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| HG02258 | hp2 | a0001 | c0001 | t0001 | g0263 | AFR | ACB | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| HG02273 | hp1 | a0002 | c0002 | t0002 | g0037 | AMR | PEL | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| HG02273 | hp2 | a0001 | c0001 | t0001 | g0081 | AMR | PEL | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| HG02280 | hp1 | a0001 | c0001 | t0001 | g0262 | AFR | ACB | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| HG02280 | hp2 | a0002 | c0002 | t0002 | g0250 | AFR | ACB | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| HG02300 | hp1 | a0002 | c0002 | t0002 | g0110 | AMR | PEL | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| HG02300 | hp2 | a0001 | c0001 | t0001 | g0113 | AMR | PEL | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| HG02451 | hp1 | a0002 | c0002 | t0004 | g0205 | AFR | ACB | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| HG02451 | hp2 | a0001 | c0001 | t0001 | g0266 | AFR | ACB | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| HG02523 | hp1 | a0001 | c0001 | t0001 | g0093 | EAS | KHV | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| HG02523 | hp2 | a0001 | c0001 | t0001 | g0216 | EAS | KHV | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| HG02572 | hp1 | a0001 | c0001 | t0003 | g0267 | AFR | GWD | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| HG02572 | hp2 | a0002 | c0002 | t0002 | g0185 | AFR | GWD | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| HG02602 | hp1 | a0001 | c0001 | t0001 | g0222 | SAS | PJL | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| HG02602 | hp2 | a0001 | c0001 | t0001 | g0084 | SAS | PJL | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| HG02622 | hp1 | a0002 | c0002 | t0002 | g0162 | AFR | GWD | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| HG02622 | hp2 | a0001 | c0001 | t0001 | g0152 | AFR | GWD | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| HG02630 | hp1 | a0001 | c0001 | t0001 | g0270 | AFR | GWD | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| HG02630 | hp2 | a0002 | c0002 | t0002 | g0156 | AFR | GWD | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| HG02647 | hp1 | a0002 | c0002 | t0002 | g0175 | AFR | GWD | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| HG02647 | hp2 | a0003 | c0004 | t0001 | g0241 | AFR | GWD | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| HG02683 | hp1 | a0002 | c0002 | t0002 | g0039 | SAS | PJL | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| HG02683 | hp2 | a0001 | c0001 | t0001 | g0057 | SAS | PJL | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| HG02698 | hp1 | a0002 | c0002 | t0002 | g0158 | SAS | PJL | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| HG02698 | hp2 | a0001 | c0001 | t0001 | g0102 | SAS | PJL | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| HG02717 | hp1 | a0002 | c0002 | t0002 | g0153 | AFR | GWD | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| HG02717 | hp2 | a0001 | c0003 | t0001 | g0229 | AFR | GWD | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| HG02723 | hp1 | a0002 | c0002 | t0002 | g0177 | AFR | GWD | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| HG02723 | hp2 | a0002 | c0002 | t0002 | g0275 | AFR | GWD | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| HG02735 | hp1 | a0002 | c0002 | t0002 | g0181 | SAS | PJL | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| HG02735 | hp2 | a0001 | c0003 | t0001 | g0238 | SAS | PJL | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| HG02738 | hp1 | a0001 | c0001 | t0001 | g0129 | SAS | PJL | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| HG02738 | hp2 | a0001 | c0001 | t0001 | g0088 | SAS | PJL | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| HG02809 | hp1 | a0001 | c0001 | t0001 | g0008 | AFR | GWD | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| HG02809 | hp2 | a0001 | c0001 | t0001 | g0112 | AFR | GWD | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| HG02818 | hp1 | a0002 | c0002 | t0002 | g0134 | AFR | GWD | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| HG02818 | hp2 | a0001 | c0001 | t0001 | g0053 | AFR | GWD | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| HG02886 | hp1 | a0002 | c0002 | t0002 | g0133 | AFR | GWD | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| HG02886 | hp2 | a0001 | c0001 | t0001 | g0007 | AFR | GWD | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| HG02895 | hp1 | a0001 | c0001 | t0001 | g0203 | AFR | GWD | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| HG02895 | hp2 | a0001 | c0001 | t0001 | g0033 | AFR | GWD | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| HG02896 | hp1 | a0001 | c0003 | t0003 | g0232 | AFR | GWD | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| HG02896 | hp2 | a0001 | c0001 | t0001 | g0259 | AFR | GWD | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| HG02897 | hp1 | a0001 | c0003 | t0003 | g0231 | AFR | GWD | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| HG02897 | hp2 | a0001 | c0001 | t0001 | g0204 | AFR | GWD | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| HG02922 | hp1 | a0001 | c0001 | t0001 | g0254 | AFR | ESN | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| HG02922 | hp2 | a0001 | c0001 | t0001 | g0257 | AFR | ESN | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| HG02965 | hp1 | a0001 | c0001 | t0001 | g0122 | AFR | ESN | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| HG02965 | hp2 | a0001 | c0001 | t0003 | g0278 | AFR | ESN | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| HG02970 | hp1 | a0002 | c0002 | t0004 | g0274 | AFR | ESN | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| HG02970 | hp2 | a0001 | c0001 | t0001 | g0124 | AFR | ESN | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| HG02976 | hp1 | a0002 | c0002 | t0002 | g0142 | AFR | ESN | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| HG02976 | hp2 | a0001 | c0001 | t0001 | g0226 | AFR | ESN | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| HG03098 | hp1 | a0002 | c0002 | t0002 | g0201 | AFR | MSL | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| HG03098 | hp2 | a0002 | c0002 | t0002 | g0145 | AFR | MSL | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| HG03130 | hp1 | a0001 | c0001 | t0001 | g0002 | AFR | ESN | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| HG03130 | hp2 | a0002 | c0002 | t0002 | g0176 | AFR | ESN | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| HG03139 | hp1 | a0002 | c0002 | t0002 | g0161 | AFR | ESN | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| HG03139 | hp2 | a0002 | c0002 | t0002 | g0261 | AFR | ESN | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| HG03195 | hp1 | a0001 | c0001 | t0001 | g0002 | AFR | ESN | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| HG03195 | hp2 | a0001 | c0001 | t0001 | g0032 | AFR | ESN | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| HG03209 | hp1 | a0001 | c0001 | t0011 | g0269 | AFR | MSL | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| HG03209 | hp2 | a0001 | c0001 | t0001 | g0255 | AFR | MSL | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| HG03225 | hp1 | a0001 | c0001 | t0001 | g0258 | AFR | MSL | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| HG03225 | hp2 | a0002 | c0002 | t0002 | g0154 | AFR | MSL | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| HG03239 | hp1 | a0001 | c0001 | t0001 | g0095 | SAS | PJL | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| HG03239 | hp2 | a0001 | c0003 | t0003 | g0245 | SAS | PJL | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| HG03453 | hp1 | a0001 | c0001 | t0001 | g0265 | AFR | MSL | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| HG03453 | hp2 | a0001 | c0001 | t0001 | g0060 | AFR | MSL | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| HG03486 | hp1 | a0002 | c0002 | t0002 | g0004 | AFR | MSL | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| HG03486 | hp2 | a0001 | c0001 | t0001 | g0061 | AFR | MSL | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| HG03516 | hp1 | a0002 | c0002 | t0002 | g0194 | AFR | ESN | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| HG03516 | hp2 | a0003 | c0004 | t0001 | g0264 | AFR | ESN | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| HG03540 | hp1 | a0001 | c0001 | t0001 | g0005 | AFR | GWD | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| HG03540 | hp2 | a0002 | c0002 | t0002 | g0277 | AFR | GWD | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| HG03579 | hp1 | a0003 | c0004 | t0001 | g0249 | AFR | MSL | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| HG03579 | hp2 | a0002 | c0002 | t0002 | g0135 | AFR | MSL | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| HG03654 | hp1 | a0001 | c0003 | t0001 | g0240 | SAS | PJL | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| HG03654 | hp2 | a0001 | c0003 | t0003 | g0242 | SAS | PJL | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| HG03669 | hp1 | a0001 | c0001 | t0001 | g0070 | SAS | PJL | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| HG03669 | hp2 | a0001 | c0003 | t0001 | g0197 | SAS | PJL | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| HG03704 | hp1 | a0001 | c0001 | t0001 | g0056 | SAS | PJL | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| HG03704 | hp2 | a0001 | c0001 | t0001 | g0219 | SAS | PJL | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| HG03831 | hp1 | a0001 | c0001 | t0001 | g0045 | SAS | BEB | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| HG03831 | hp2 | a0001 | c0001 | t0001 | g0208 | SAS | BEB | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| HG03834 | hp1 | a0001 | c0001 | t0001 | g0059 | SAS | BEB | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| HG03834 | hp2 | a0001 | c0001 | t0001 | g0221 | SAS | BEB | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| HG03942 | hp1 | a0001 | c0001 | t0001 | g0223 | SAS | BEB | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| HG03942 | hp2 | a0001 | c0003 | t0003 | g0243 | SAS | BEB | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| HG04115 | hp1 | a0002 | c0002 | t0002 | g0166 | SAS | STU | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| HG04115 | hp2 | a0001 | c0003 | t0001 | g0239 | SAS | STU | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| HG04184 | hp1 | a0002 | c0002 | t0002 | g0151 | SAS | BEB | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| HG04184 | hp2 | a0001 | c0001 | t0001 | g0026 | SAS | BEB | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| HG04199 | hp1 | a0002 | c0002 | t0010 | g0157 | SAS | STU | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| HG04199 | hp2 | a0001 | c0003 | t0001 | g0198 | SAS | STU | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| HG04204 | hp1 | a0001 | c0001 | t0001 | g0224 | SAS | STU | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| HG04204 | hp2 | a0001 | c0001 | t0001 | g0036 | SAS | STU | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| NA18522 | hp1 | a0001 | c0001 | t0001 | g0006 | AFR | YRI | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| NA18522 | hp2 | a0001 | c0001 | t0003 | g0268 | AFR | YRI | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| NA18612 | hp1 | a0001 | c0001 | t0001 | g0100 | EAS | CHB | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| NA18612 | hp2 | a0001 | c0001 | t0003 | g0067 | EAS | CHB | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| NA18747 | hp1 | a0001 | c0001 | t0003 | g0017 | EAS | CHB | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| NA18747 | hp2 | a0001 | c0001 | t0001 | g0107 | EAS | CHB | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| NA18906 | hp1 | a0001 | c0001 | t0001 | g0271 | AFR | YRI | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| NA18906 | hp2 | a0002 | c0002 | t0008 | g0003 | AFR | YRI | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| NA18941 | hp1 | a0002 | c0002 | t0002 | g0149 | EAS | JPT | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| NA18941 | hp2 | a0001 | c0001 | t0001 | g0089 | EAS | JPT | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| NA18943 | hp1 | a0001 | c0001 | t0001 | g0106 | EAS | JPT | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| NA18943 | hp2 | a0002 | c0002 | t0002 | g0136 | EAS | JPT | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| NA18944 | hp1 | a0001 | c0001 | t0001 | g0199 | EAS | JPT | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| NA18944 | hp2 | a0002 | c0002 | t0002 | g0173 | EAS | JPT | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| NA18945 | hp1 | a0001 | c0001 | t0003 | g0018 | EAS | JPT | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| NA18945 | hp2 | a0001 | c0001 | t0001 | g0071 | EAS | JPT | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| NA18948 | hp1 | a0001 | c0001 | t0003 | g0015 | EAS | JPT | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| NA18948 | hp2 | a0001 | c0001 | t0001 | g0096 | EAS | JPT | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| NA18949 | hp1 | a0001 | c0001 | t0001 | g0075 | EAS | JPT | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| NA18949 | hp2 | a0002 | c0002 | t0002 | g0179 | EAS | JPT | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| NA18952 | hp1 | a0001 | c0001 | t0001 | g0092 | EAS | JPT | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| NA18952 | hp2 | a0002 | c0002 | t0002 | g0137 | EAS | JPT | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| NA18953 | hp1 | a0001 | c0001 | t0001 | g0196 | EAS | JPT | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| NA18953 | hp2 | a0002 | c0002 | t0002 | g0131 | EAS | JPT | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| NA18960 | hp1 | a0001 | c0001 | t0003 | g0022 | EAS | JPT | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| NA18960 | hp2 | a0001 | c0001 | t0001 | g0098 | EAS | JPT | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| NA18962 | hp1 | a0001 | c0001 | t0001 | g0058 | EAS | JPT | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| NA18962 | hp2 | a0002 | c0002 | t0002 | g0171 | EAS | JPT | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| NA18964 | hp1 | a0002 | c0002 | t0002 | g0182 | EAS | JPT | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| NA18964 | hp2 | a0001 | c0001 | t0003 | g0016 | EAS | JPT | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| NA18966 | hp1 | a0001 | c0001 | t0001 | g0041 | EAS | JPT | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| NA18966 | hp2 | a0001 | c0001 | t0001 | g0210 | EAS | JPT | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| NA18969 | hp1 | a0002 | c0002 | t0002 | g0172 | EAS | JPT | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| NA18969 | hp2 | a0001 | c0001 | t0001 | g0101 | EAS | JPT | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| NA18971 | hp1 | a0001 | c0001 | t0001 | g0213 | EAS | JPT | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| NA18971 | hp2 | a0001 | c0001 | t0001 | g0090 | EAS | JPT | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| NA18973 | hp1 | a0001 | c0001 | t0001 | g0211 | EAS | JPT | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| NA18973 | hp2 | a0001 | c0001 | t0001 | g0087 | EAS | JPT | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| NA18982 | hp1 | a0001 | c0001 | t0001 | g0034 | EAS | JPT | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| NA18982 | hp2 | a0002 | c0002 | t0002 | g0190 | EAS | JPT | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| NA19000 | hp1 | a0002 | c0002 | t0002 | g0126 | EAS | JPT | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| NA19000 | hp2 | a0001 | c0001 | t0001 | g0105 | EAS | JPT | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| NA19001 | hp1 | a0002 | c0002 | t0002 | g0184 | EAS | JPT | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| NA19001 | hp2 | a0001 | c0001 | t0001 | g0094 | EAS | JPT | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| NA19005 | hp1 | a0001 | c0001 | t0003 | g0019 | EAS | JPT | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| NA19005 | hp2 | a0001 | c0001 | t0001 | g0050 | EAS | JPT | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| NA19007 | hp1 | a0001 | c0001 | t0003 | g0013 | EAS | JPT | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| NA19007 | hp2 | a0001 | c0001 | t0001 | g0040 | EAS | JPT | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| NA19010 | hp1 | a0001 | c0001 | t0001 | g0083 | EAS | JPT | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| NA19010 | hp2 | a0002 | c0002 | t0002 | g0178 | EAS | JPT | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| NA19011 | hp1 | a0001 | c0001 | t0001 | g0214 | EAS | JPT | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| NA19011 | hp2 | a0001 | c0001 | t0001 | g0104 | EAS | JPT | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| NA19030 | hp1 | a0002 | c0002 | t0005 | g0207 | AFR | LWK | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| NA19030 | hp2 | a0001 | c0001 | t0001 | g0260 | AFR | LWK | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| NA19043 | hp1 | a0002 | c0002 | t0009 | g0200 | AFR | LWK | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| NA19043 | hp2 | a0001 | c0001 | t0001 | g0256 | AFR | LWK | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| NA19060 | hp1 | a0002 | c0002 | t0002 | g0191 | EAS | JPT | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| NA19060 | hp2 | a0001 | c0001 | t0001 | g0082 | EAS | JPT | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| NA19063 | hp1 | a0002 | c0002 | t0002 | g0228 | EAS | JPT | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| NA19063 | hp2 | a0001 | c0001 | t0001 | g0076 | EAS | JPT | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| NA19064 | hp1 | a0001 | c0001 | t0003 | g0103 | EAS | JPT | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| NA19064 | hp2 | a0002 | c0002 | t0002 | g0148 | EAS | JPT | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| NA19068 | hp1 | a0002 | c0002 | t0002 | g0116 | EAS | JPT | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| NA19068 | hp2 | a0001 | c0001 | t0001 | g0063 | EAS | JPT | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| NA19070 | hp1 | a0001 | c0001 | t0003 | g0020 | EAS | JPT | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| NA19070 | hp2 | a0001 | c0001 | t0001 | g0035 | EAS | JPT | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| NA19079 | hp1 | a0001 | c0001 | t0003 | g0024 | EAS | JPT | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| NA19079 | hp2 | a0001 | c0001 | t0001 | g0209 | EAS | JPT | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| NA19080 | hp1 | a0001 | c0001 | t0001 | g0043 | EAS | JPT | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| NA19080 | hp2 | a0001 | c0001 | t0001 | g0212 | EAS | JPT | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| NA19084 | hp1 | a0001 | c0001 | t0001 | g0115 | EAS | JPT | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| NA19084 | hp2 | a0002 | c0002 | t0002 | g0143 | EAS | JPT | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| NA19085 | hp1 | a0001 | c0001 | t0003 | g0014 | EAS | JPT | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| NA19085 | hp2 | a0001 | c0001 | t0001 | g0074 | EAS | JPT | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| NA19090 | hp1 | a0002 | c0002 | t0002 | g0117 | EAS | JPT | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| NA19090 | hp2 | a0001 | c0001 | t0001 | g0048 | EAS | JPT | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| NA20129 | hp1 | a0001 | c0001 | t0001 | g0120 | AFR | ASW | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| NA20129 | hp2 | a0002 | c0002 | t0002 | g0192 | AFR | ASW | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| NA20752 | hp1 | a0001 | c0001 | t0001 | g0078 | EUR | TSI | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| NA20752 | hp2 | a0001 | c0003 | t0001 | g0227 | EUR | TSI | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| NA20805 | hp1 | a0001 | c0003 | t0003 | g0246 | EUR | TSI | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| NA20805 | hp2 | a0001 | c0001 | t0001 | g0079 | EUR | TSI | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| NA20905 | hp1 | a0001 | c0001 | t0001 | g0128 | SAS | GIH | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| NA20905 | hp2 | a0002 | c0002 | t0002 | g0027 | SAS | GIH | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| HG01123 | hp1 | a0001 | c0001 | t0001 | g0080 | AMR | CLM | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| HG01123 | hp2 | a0002 | c0002 | t0002 | g0141 | AMR | CLM | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| HG02559 | hp1 | a0002 | c0002 | t0002 | g0193 | AFR | ACB | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| HG02559 | hp2 | a0001 | c0001 | t0001 | g0202 | AFR | ACB | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| HG03471 | hp1 | a0002 | c0002 | t0002 | g0144 | AFR | MSL | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| HG03471 | hp2 | a0001 | c0001 | t0001 | g0062 | AFR | MSL | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| HG06807 | hp1 | a0001 | c0001 | t0003 | g0206 | AFR | USA | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| HG06807 | hp2 | a0002 | c0002 | t0002 | g0252 | AFR | USA | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| NA20300 | hp1 | a0002 | c0002 | t0002 | g0251 | AFR | USA | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| NA20300 | hp2 | a0001 | c0001 | t0001 | g0054 | AFR | USA | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| homoSapiens | chm13v2 | a0002 | c0002 | t0002 | g0130 | REF | REF | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0001 | g0276 | REF | REF | HSD17B12_chr11_43675738_43861615 | HSD17B12 | chr11 | 43675738 | 43861615 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr11:43680844 | C | T | 1 | a0004 | 2 | HG01099.hp2 HG01106.hp2 |
missense_variant | MODERATE | c.17C>T | p.Pro6Leu | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/11 | 107/2396 | 17/939 | 6/312 | chr11 | 43680844 | |||
| chr11:43838378 | A | G | 1 | a0003 | 3 | HG02647.hp2 HG03516.hp2 HG03579.hp1 |
missense_variant | MODERATE | c.598A>G | p.Thr200Ala | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 8/11 | 688/2396 | 598/939 | 200/312 | chr11 | 43838378 | |||
| chr11:43855148 | C | T | 2 | a0002 a0004 |
99 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(96): Show |
missense_variant | MODERATE | c.839C>T | p.Ser280Leu | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 11/11 | 929/2396 | 839/939 | 280/312 | chr11 | 43855148 | |||
| chr11:43855221 | C | G | 1 | a0005 | 1 | HG00609.hp2 | missense_variant | MODERATE | c.912C>G | p.His304Gln | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 11/11 | 1002/2396 | 912/939 | 304/312 | chr11 | 43855221 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr11:43680980 | A | G | 3 | a0001c0003 a0001c0007 a0003c0004 |
28 | HG00140.hp1 HG00639.hp2 HG00642.hp2 others(25): Show |
synonymous_variant | LOW | c.153A>G | p.Glu51Glu | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/11 | 243/2396 | 153/939 | 51/312 | chr11 | 43680980 | |||
| chr11:43854855 | T | C | 1 | a0001c0007 | 1 | HG02258.hp1 | synonymous_variant | LOW | c.825T>C | p.His275His | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 10/11 | 915/2396 | 825/939 | 275/312 | chr11 | 43854855 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr11:43855263 | A | C | 4 | a0001c0001t0003 a0001c0001t0011 a0001c0003t0003 others(1): Show |
28 | HG00280.hp1 HG00609.hp2 HG01070.hp2 others(25): Show |
3_prime_UTR_variant | MODIFIER | c.*15A>C | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 11/11 | 15 | chr11 | 43855263 | ||||||
| chr11:43855279 | A | G | 4 | a0001c0001t0003 a0001c0001t0011 a0001c0003t0003 others(1): Show |
28 | HG00280.hp1 HG00609.hp2 HG01070.hp2 others(25): Show |
3_prime_UTR_variant | MODIFIER | c.*31A>G | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 11/11 | 31 | chr11 | 43855279 | ||||||
| chr11:43855296 | C | T | 1 | a0005c0006t0012 | 1 | HG00609.hp2 | 3_prime_UTR_variant | MODIFIER | c.*48C>T | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 11/11 | 48 | chr11 | 43855296 | ||||||
| chr11:43855513 | A | G | 1 | a0001c0001t0011 | 1 | HG03209.hp1 | 3_prime_UTR_variant | MODIFIER | c.*265A>G | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 11/11 | 265 | chr11 | 43855513 | ||||||
| chr11:43855582 | C | T | 1 | a0002c0002t0010 | 1 | HG04199.hp1 | 3_prime_UTR_variant | MODIFIER | c.*334C>T | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 11/11 | 334 | chr11 | 43855582 | ||||||
| chr11:43855654 | CTTTTGT | C | 6 | a0002c0002t0002 a0002c0002t0005 a0002c0002t0006 others(3): Show |
95 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(92): Show |
3_prime_UTR_variant | MODIFIER | c.*412_*417delTTTTTG | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 11/11 | 412 | INFO_REALIGN_3_PRIME | chr11 | 43855654 | |||||
| chr11:43855889 | T | TCTCAGTT others(309): Show |
1 | a0002c0002t0005 | 1 | NA19030.hp1 | 3_prime_UTR_variant | MODIFIER | c.*650_*651insTTTTTT others(310): Show |
HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 11/11 | 651 | INFO_REALIGN_3_PRIME | chr11 | 43855889 | |||||
| chr11:43855889 | T | TCTCAGTT others(309): Show |
1 | a0002c0002t0006 | 1 | HG00735.hp1 | 3_prime_UTR_variant | MODIFIER | c.*650_*651insTTTTTT others(310): Show |
HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 11/11 | 651 | INFO_REALIGN_3_PRIME | chr11 | 43855889 | |||||
| chr11:43855889 | T | TCTCAGTT others(309): Show |
4 | a0002c0002t0002 a0002c0002t0007 a0002c0002t0010 others(1): Show |
93 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(90): Show |
3_prime_UTR_variant | MODIFIER | c.*650_*651insTTTTTT others(310): Show |
HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 11/11 | 651 | INFO_REALIGN_3_PRIME | chr11 | 43855889 | |||||
| chr11:43855889 | T | TCTCAGTT others(309): Show |
1 | a0002c0002t0004 | 2 | HG02451.hp1 HG02970.hp1 |
3_prime_UTR_variant | MODIFIER | c.*650_*651insTTTTTT others(310): Show |
HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 11/11 | 651 | INFO_REALIGN_3_PRIME | chr11 | 43855889 | |||||
| chr11:43855889 | T | TCTCAGTT others(309): Show |
1 | a0002c0002t0008 | 1 | NA18906.hp2 | 3_prime_UTR_variant | MODIFIER | c.*650_*651insTTTTTT others(310): Show |
HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 11/11 | 651 | INFO_REALIGN_3_PRIME | chr11 | 43855889 | |||||
| chr11:43855889 | T | TCTCAGTT others(309): Show |
1 | a0002c0002t0009 | 1 | NA19043.hp1 | 3_prime_UTR_variant | MODIFIER | c.*650_*651insTTTTTT others(310): Show |
HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 11/11 | 651 | INFO_REALIGN_3_PRIME | chr11 | 43855889 | |||||
| chr11:43856384 | C | A | 8 | a0002c0002t0002 a0002c0002t0004 a0002c0002t0005 others(5): Show |
98 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(95): Show |
3_prime_UTR_variant | MODIFIER | c.*1136C>A | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 11/11 | 1136 | chr11 | 43856384 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr11:43681031 | G | A | 195 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(192): Show |
197 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(194): Show |
intron_variant | MODIFIER | c.160+44G>A | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43681031 | |||||||
| chr11:43681040 | C | A | 8 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(5): Show |
8 | HG01261.hp2 HG02257.hp1 HG02809.hp1 others(5): Show |
intron_variant | MODIFIER | c.160+53C>A | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43681040 | |||||||
| chr11:43681065 | G | C | 273 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(270): Show |
275 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(272): Show |
intron_variant | MODIFIER | c.160+78G>C | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43681065 | |||||||
| chr11:43681164 | A | T | 1 | a0002c0002t0004g0274 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.160+177A>T | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43681164 | |||||||
| chr11:43681294 | A | G | 1 | a0001c0003t0001g0273 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.160+307A>G | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43681294 | |||||||
| chr11:43681333 | C | T | 1 | a0001c0003t0001g0272 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.160+346C>T | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43681333 | |||||||
| chr11:43681409 | G | T | 1 | a0001c0001t0001g0271 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.160+422G>T | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43681409 | |||||||
| chr11:43681423 | G | A | 2 | a0004c0005t0002g0011 a0004c0005t0002g0012 |
2 | HG01099.hp2 HG01106.hp2 |
intron_variant | MODIFIER | c.160+436G>A | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43681423 | |||||||
| chr11:43681437 | T | C | 1 | a0002c0002t0008g0003 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.160+450T>C | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43681437 | |||||||
| chr11:43681500 | A | AATCGTAC others(6): Show |
1 | a0001c0001t0001g0270 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.160+515_160+527dup others(13): Show |
HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr11 | 43681500 | ||||||
| chr11:43681566 | A | G | 12 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(9): Show |
12 | HG01261.hp2 HG02257.hp1 HG02572.hp1 others(9): Show |
intron_variant | MODIFIER | c.160+579A>G | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43681566 | |||||||
| chr11:43681645 | T | C | 12 | a0001c0001t0003g0013 a0001c0001t0003g0014 a0001c0001t0003g0015 others(9): Show |
12 | HG00280.hp1 HG00609.hp2 NA18747.hp1 others(9): Show |
intron_variant | MODIFIER | c.160+658T>C | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43681645 | |||||||
| chr11:43681646 | G | A | 2 | a0001c0003t0001g0197 a0001c0003t0001g0198 |
2 | HG03669.hp2 HG04199.hp2 |
intron_variant | MODIFIER | c.160+659G>A | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43681646 | |||||||
| chr11:43681670 | AT | A | 103 | a0001c0001t0001g0026 a0001c0001t0001g0028 a0001c0001t0001g0029 others(100): Show |
104 | HG00323.hp2 HG00408.hp1 HG00423.hp1 others(101): Show |
intron_variant | MODIFIER | c.160+698delT | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr11 | 43681670 | ||||||
| chr11:43681685 | T | C | 104 | a0001c0001t0001g0002 a0001c0001t0001g0115 a0001c0001t0001g0120 others(101): Show |
105 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(102): Show |
intron_variant | MODIFIER | c.160+698T>C | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43681685 | |||||||
| chr11:43681824 | TC | T | 22 | a0001c0001t0001g0111 a0001c0001t0001g0112 a0001c0001t0001g0113 others(19): Show |
22 | HG00280.hp1 HG00609.hp2 HG02055.hp1 others(19): Show |
intron_variant | MODIFIER | c.160+847delC | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr11 | 43681824 | ||||||
| chr11:43681834 | C | CT | 23 | a0001c0001t0001g0199 a0001c0001t0001g0208 a0001c0001t0001g0209 others(20): Show |
23 | HG00099.hp2 HG00140.hp1 HG01167.hp2 others(20): Show |
intron_variant | MODIFIER | c.160+857dupT | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr11 | 43681834 | ||||||
| chr11:43681834 | CT | C | 29 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(26): Show |
29 | HG00639.hp2 HG00642.hp2 HG01069.hp1 others(26): Show |
intron_variant | MODIFIER | c.160+857delT | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr11 | 43681834 | ||||||
| chr11:43681835 | T | C | 3 | a0001c0001t0001g0254 a0001c0003t0001g0198 a0003c0004t0001g0264 |
3 | HG02922.hp1 HG03516.hp2 HG04199.hp2 |
intron_variant | MODIFIER | c.160+848T>C | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43681835 | |||||||
| chr11:43681895 | C | T | 1 | a0002c0002t0002g0110 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.160+908C>T | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43681895 | |||||||
| chr11:43681967 | T | G | 2 | a0001c0001t0001g0115 a0002c0002t0002g0116 |
2 | NA19068.hp1 NA19084.hp1 |
intron_variant | MODIFIER | c.160+980T>G | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43681967 | |||||||
| chr11:43682030 | T | C | 3 | a0002c0002t0002g0117 a0002c0002t0002g0118 a0002c0002t0002g0119 |
3 | HG00408.hp2 HG02135.hp1 NA19090.hp1 |
intron_variant | MODIFIER | c.160+1043T>C | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43682030 | |||||||
| chr11:43682434 | C | T | 1 | a0003c0004t0001g0249 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.160+1447C>T | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43682434 | |||||||
| chr11:43682490 | C | G | 110 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(107): Show |
110 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(107): Show |
intron_variant | MODIFIER | c.160+1503C>G | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43682490 | |||||||
| chr11:43682496 | C | T | 1 | a0002c0002t0002g0201 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.160+1509C>T | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43682496 | |||||||
| chr11:43682497 | A | G | 1 | a0002c0002t0002g0201 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.160+1510A>G | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43682497 | |||||||
| chr11:43682498 | T | C | 1 | a0002c0002t0002g0201 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.160+1511T>C | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43682498 | |||||||
| chr11:43682508 | C | G | 1 | a0002c0002t0002g0201 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.160+1521C>G | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43682508 | |||||||
| chr11:43682508 | CTCCA | C | 113 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(110): Show |
113 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(110): Show |
intron_variant | MODIFIER | c.160+1526_160+1529d others(6): Show |
HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr11 | 43682508 | ||||||
| chr11:43682512 | A | G | 1 | a0002c0002t0002g0201 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.160+1525A>G | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43682512 | |||||||
| chr11:43682516 | A | G | 1 | a0002c0002t0002g0201 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.160+1529A>G | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43682516 | |||||||
| chr11:43682517 | G | A | 1 | a0002c0002t0002g0201 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.160+1530G>A | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43682517 | |||||||
| chr11:43682524 | T | C | 1 | a0002c0002t0002g0201 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.160+1537T>C | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43682524 | |||||||
| chr11:43682540 | A | G | 1 | a0002c0002t0002g0201 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.160+1553A>G | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43682540 | |||||||
| chr11:43682544 | C | CAAAAAAA others(12): Show |
1 | a0002c0002t0002g0201 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.160+1561_160+1579d others(21): Show |
HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr11 | 43682544 | ||||||
| chr11:43682544 | CA | C | 41 | a0001c0001t0001g0002 a0001c0001t0001g0026 a0001c0001t0001g0028 others(38): Show |
42 | HG00099.hp2 HG00140.hp1 HG00642.hp1 others(39): Show |
intron_variant | MODIFIER | c.160+1579delA | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr11 | 43682544 | ||||||
| chr11:43682544 | CAA | C | 100 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(97): Show |
101 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(98): Show |
intron_variant | MODIFIER | c.160+1578_160+1579d others(4): Show |
HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr11 | 43682544 | ||||||
| chr11:43682544 | CAAA | C | 120 | a0001c0001t0001g0068 a0001c0001t0001g0069 a0001c0001t0001g0070 others(117): Show |
120 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(117): Show |
intron_variant | MODIFIER | c.160+1577_160+1579d others(5): Show |
HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr11 | 43682544 | ||||||
| chr11:43682560 | A | C | 110 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(107): Show |
110 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(107): Show |
intron_variant | MODIFIER | c.160+1573A>C | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43682560 | |||||||
| chr11:43682593 | A | G | 7 | a0001c0003t0003g0242 a0001c0003t0003g0243 a0001c0003t0003g0244 others(4): Show |
7 | HG01070.hp2 HG01071.hp1 HG02004.hp1 others(4): Show |
intron_variant | MODIFIER | c.160+1606A>G | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43682593 | |||||||
| chr11:43682790 | C | CT | 106 | a0001c0001t0001g0002 a0001c0001t0001g0026 a0001c0001t0001g0028 others(103): Show |
108 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(105): Show |
intron_variant | MODIFIER | c.160+1814dupT | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr11 | 43682790 | ||||||
| chr11:43682965 | T | G | 115 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(112): Show |
115 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(112): Show |
intron_variant | MODIFIER | c.160+1978T>G | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43682965 | |||||||
| chr11:43682972 | T | A | 226 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(223): Show |
227 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(224): Show |
intron_variant | MODIFIER | c.160+1985T>A | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43682972 | |||||||
| chr11:43683085 | C | A | 23 | a0001c0001t0001g0199 a0001c0001t0001g0208 a0001c0001t0001g0209 others(20): Show |
23 | HG00099.hp2 HG00140.hp1 HG01167.hp2 others(20): Show |
intron_variant | MODIFIER | c.160+2098C>A | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43683085 | |||||||
| chr11:43683096 | T | G | 115 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(112): Show |
115 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(112): Show |
intron_variant | MODIFIER | c.160+2109T>G | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43683096 | |||||||
| chr11:43683097 | T | G | 1 | a0001c0001t0001g0005 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.160+2110T>G | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43683097 | |||||||
| chr11:43683104 | G | GT | 17 | a0001c0001t0001g0106 a0001c0001t0001g0107 a0001c0001t0001g0208 others(14): Show |
17 | HG00099.hp2 HG00140.hp1 HG01167.hp2 others(14): Show |
intron_variant | MODIFIER | c.160+2132dupT | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr11 | 43683104 | ||||||
| chr11:43683104 | G | T | 128 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(125): Show |
128 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(125): Show |
intron_variant | MODIFIER | c.160+2117G>T | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43683104 | |||||||
| chr11:43683107 | T | G | 115 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(112): Show |
115 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(112): Show |
intron_variant | MODIFIER | c.160+2120T>G | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43683107 | |||||||
| chr11:43683962 | G | T | 2 | a0001c0001t0001g0111 a0001c0001t0001g0112 |
2 | HG02055.hp1 HG02809.hp2 |
intron_variant | MODIFIER | c.160+2975G>T | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43683962 | |||||||
| chr11:43684041 | T | G | 1 | a0001c0001t0001g0029 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.160+3054T>G | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43684041 | |||||||
| chr11:43684073 | C | G | 114 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(111): Show |
114 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(111): Show |
intron_variant | MODIFIER | c.160+3086C>G | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43684073 | |||||||
| chr11:43684118 | G | T | 1 | a0001c0001t0001g0216 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.160+3131G>T | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43684118 | |||||||
| chr11:43684727 | G | A | 1 | a0002c0002t0002g0127 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.160+3740G>A | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43684727 | |||||||
| chr11:43684773 | G | A | 2 | a0001c0001t0001g0030 a0001c0001t0001g0031 |
2 | HG01168.hp1 HG01258.hp2 |
intron_variant | MODIFIER | c.160+3786G>A | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43684773 | |||||||
| chr11:43684784 | A | G | 1 | a0002c0002t0008g0003 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.160+3797A>G | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43684784 | |||||||
| chr11:43685119 | C | G | 1 | a0002c0002t0002g0066 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.160+4132C>G | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43685119 | |||||||
| chr11:43685284 | T | TACTTTGC others(14): Show |
10 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(7): Show |
10 | HG01261.hp2 HG02257.hp1 HG02258.hp1 others(7): Show |
intron_variant | MODIFIER | c.160+4297_160+4298i others(23): Show |
HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43685284 | |||||||
| chr11:43685286 | C | A | 10 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(7): Show |
10 | HG01261.hp2 HG02257.hp1 HG02258.hp1 others(7): Show |
intron_variant | MODIFIER | c.160+4299C>A | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43685286 | |||||||
| chr11:43685286 | C | CTTTGCTT others(14): Show |
239 | a0001c0001t0001g0026 a0001c0001t0001g0028 a0001c0001t0001g0029 others(236): Show |
240 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(237): Show |
intron_variant | MODIFIER | c.160+4299_160+4300i others(23): Show |
HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43685286 | |||||||
| chr11:43685382 | G | T | 3 | a0001c0001t0001g0262 a0001c0001t0001g0263 a0002c0002t0002g0261 |
3 | HG02258.hp2 HG02280.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.160+4395G>T | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43685382 | |||||||
| chr11:43685390 | A | G | 1 | a0002c0002t0005g0207 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.160+4403A>G | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43685390 | |||||||
| chr11:43685582 | C | T | 1 | a0001c0001t0001g0226 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.160+4595C>T | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43685582 | |||||||
| chr11:43685814 | C | T | 76 | a0001c0001t0001g0152 a0001c0001t0001g0186 a0001c0001t0001g0265 others(73): Show |
76 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(73): Show |
intron_variant | MODIFIER | c.160+4827C>T | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43685814 | |||||||
| chr11:43686010 | T | A | 114 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(111): Show |
114 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(111): Show |
intron_variant | MODIFIER | c.160+5023T>A | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43686010 | |||||||
| chr11:43686093 | G | A | 1 | a0001c0001t0001g0069 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.160+5106G>A | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43686093 | |||||||
| chr11:43686342 | A | G | 2 | a0001c0003t0003g0231 a0001c0003t0003g0232 |
2 | HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.160+5355A>G | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43686342 | |||||||
| chr11:43686351 | G | A | 1 | a0001c0003t0003g0242 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.160+5364G>A | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43686351 | |||||||
| chr11:43686361 | A | G | 2 | a0002c0002t0002g0190 a0002c0002t0002g0191 |
2 | NA18982.hp2 NA19060.hp1 |
intron_variant | MODIFIER | c.160+5374A>G | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43686361 | |||||||
| chr11:43686525 | C | T | 1 | a0002c0002t0002g0004 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.160+5538C>T | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43686525 | |||||||
| chr11:43686579 | C | T | 1 | a0001c0001t0001g0260 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.160+5592C>T | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43686579 | |||||||
| chr11:43686581 | A | G | 3 | a0002c0002t0002g0187 a0002c0002t0002g0188 a0002c0002t0002g0189 |
3 | HG00140.hp2 HG01167.hp1 HG01346.hp1 |
intron_variant | MODIFIER | c.160+5594A>G | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43686581 | |||||||
| chr11:43686595 | G | GT | 181 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(178): Show |
183 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(180): Show |
intron_variant | MODIFIER | c.160+5625dupT | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr11 | 43686595 | ||||||
| chr11:43686595 | G | GTT | 8 | a0001c0001t0001g0065 a0001c0001t0001g0105 a0001c0001t0001g0186 others(5): Show |
8 | HG01099.hp2 HG01106.hp2 HG01192.hp1 others(5): Show |
intron_variant | MODIFIER | c.160+5624_160+5625d others(4): Show |
HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr11 | 43686595 | ||||||
| chr11:43686595 | GT | G | 32 | a0001c0001t0001g0199 a0001c0001t0001g0208 a0001c0001t0001g0209 others(29): Show |
32 | HG00099.hp2 HG00140.hp1 HG00609.hp2 others(29): Show |
intron_variant | MODIFIER | c.160+5625delT | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr11 | 43686595 | ||||||
| chr11:43686859 | G | A | 117 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(114): Show |
117 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(114): Show |
intron_variant | MODIFIER | c.160+5872G>A | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43686859 | |||||||
| chr11:43687001 | T | A | 1 | a0001c0001t0001g0202 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.160+6014T>A | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43687001 | |||||||
| chr11:43687007 | CTTTCAG | C | 91 | a0001c0001t0001g0026 a0001c0001t0001g0028 a0001c0001t0001g0029 others(88): Show |
92 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(89): Show |
intron_variant | MODIFIER | c.160+6027_160+6032d others(8): Show |
HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr11 | 43687007 | ||||||
| chr11:43687030 | C | CAGA | 227 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(224): Show |
228 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(225): Show |
intron_variant | MODIFIER | c.160+6044_160+6046d others(5): Show |
HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr11 | 43687030 | ||||||
| chr11:43687152 | C | T | 227 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(224): Show |
228 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(225): Show |
intron_variant | MODIFIER | c.160+6165C>T | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43687152 | |||||||
| chr11:43687175 | C | T | 114 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(111): Show |
114 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(111): Show |
intron_variant | MODIFIER | c.160+6188C>T | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43687175 | |||||||
| chr11:43687202 | A | G | 114 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(111): Show |
114 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(111): Show |
intron_variant | MODIFIER | c.160+6215A>G | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43687202 | |||||||
| chr11:43687436 | A | G | 249 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(246): Show |
250 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(247): Show |
intron_variant | MODIFIER | c.160+6449A>G | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43687436 | |||||||
| chr11:43687836 | C | T | 91 | a0001c0001t0001g0026 a0001c0001t0001g0028 a0001c0001t0001g0029 others(88): Show |
92 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(89): Show |
intron_variant | MODIFIER | c.160+6849C>T | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43687836 | |||||||
| chr11:43687854 | C | T | 3 | a0001c0001t0001g0202 a0001c0001t0001g0203 a0001c0001t0001g0204 |
3 | HG02559.hp2 HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.160+6867C>T | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43687854 | |||||||
| chr11:43687879 | C | G | 249 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(246): Show |
250 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(247): Show |
intron_variant | MODIFIER | c.160+6892C>G | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43687879 | |||||||
| chr11:43687925 | C | T | 1 | a0001c0001t0001g0063 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.160+6938C>T | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43687925 | |||||||
| chr11:43687937 | C | T | 33 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(30): Show |
33 | HG00639.hp2 HG00642.hp2 HG01069.hp1 others(30): Show |
intron_variant | MODIFIER | c.160+6950C>T | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43687937 | |||||||
| chr11:43687986 | C | T | 1 | a0002c0002t0002g0184 | 1 | NA19001.hp1 | intron_variant | MODIFIER | c.160+6999C>T | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43687986 | |||||||
| chr11:43688176 | C | G | 1 | a0001c0001t0001g0186 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.160+7189C>G | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43688176 | |||||||
| chr11:43688211 | C | CA | 22 | a0001c0001t0001g0128 a0001c0001t0001g0129 a0001c0003t0001g0197 others(19): Show |
22 | HG00639.hp2 HG01069.hp1 HG01070.hp2 others(19): Show |
intron_variant | MODIFIER | c.160+7238dupA | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr11 | 43688211 | ||||||
| chr11:43688261 | T | C | 1 | a0001c0001t0001g0006 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.160+7274T>C | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43688261 | |||||||
| chr11:43688328 | A | G | 1 | a0002c0002t0002g0183 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.160+7341A>G | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43688328 | |||||||
| chr11:43688367 | C | T | 1 | a0001c0001t0001g0254 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.160+7380C>T | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43688367 | |||||||
| chr11:43688384 | G | A | 1 | a0001c0003t0001g0227 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.160+7397G>A | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43688384 | |||||||
| chr11:43688415 | G | T | 227 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(224): Show |
228 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(225): Show |
intron_variant | MODIFIER | c.160+7428G>T | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43688415 | |||||||
| chr11:43688519 | A | G | 1 | a0001c0001t0001g0224 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.160+7532A>G | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43688519 | |||||||
| chr11:43688527 | C | G | 3 | a0001c0001t0001g0202 a0001c0001t0001g0203 a0001c0001t0001g0204 |
3 | HG02559.hp2 HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.160+7540C>G | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43688527 | |||||||
| chr11:43688674 | C | T | 1 | a0001c0003t0001g0239 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.160+7687C>T | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43688674 | |||||||
| chr11:43688712 | T | C | 1 | a0002c0002t0002g0138 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.160+7725T>C | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43688712 | |||||||
| chr11:43689057 | G | A | 1 | a0001c0001t0001g0032 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.160+8070G>A | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43689057 | |||||||
| chr11:43689213 | A | G | 2 | a0002c0002t0002g0126 a0002c0002t0002g0182 |
2 | NA18964.hp1 NA19000.hp1 |
intron_variant | MODIFIER | c.160+8226A>G | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43689213 | |||||||
| chr11:43689844 | C | T | 1 | a0002c0002t0008g0003 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.160+8857C>T | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43689844 | |||||||
| chr11:43689912 | C | G | 1 | a0002c0002t0002g0201 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.160+8925C>G | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43689912 | |||||||
| chr11:43689919 | C | T | 3 | a0001c0001t0001g0060 a0001c0001t0001g0061 a0001c0001t0001g0062 |
3 | HG03453.hp2 HG03471.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.160+8932C>T | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43689919 | |||||||
| chr11:43690189 | C | T | 3 | a0001c0001t0001g0111 a0001c0001t0001g0112 a0001c0001t0003g0206 |
3 | HG02055.hp1 HG02809.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.160+9202C>T | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43690189 | |||||||
| chr11:43690361 | C | CAT | 4 | a0002c0002t0002g0143 a0002c0002t0002g0184 a0002c0002t0002g0187 others(1): Show |
4 | HG00140.hp2 HG02723.hp2 NA19001.hp1 others(1): Show |
intron_variant | MODIFIER | c.160+9417_160+9418d others(4): Show |
HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr11 | 43690361 | ||||||
| chr11:43690361 | C | CATAT | 3 | a0002c0002t0002g0139 a0002c0002t0002g0140 a0002c0002t0002g0141 |
3 | HG00639.hp1 HG01123.hp2 HG01515.hp2 |
intron_variant | MODIFIER | c.160+9415_160+9418d others(6): Show |
HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr11 | 43690361 | ||||||
| chr11:43690361 | C | T | 10 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(7): Show |
10 | HG01261.hp2 HG02257.hp1 HG02258.hp1 others(7): Show |
intron_variant | MODIFIER | c.160+9374C>T | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43690361 | |||||||
| chr11:43690361 | CAT | C | 16 | a0001c0001t0001g0047 a0001c0001t0001g0048 a0001c0001t0001g0060 others(13): Show |
16 | HG00323.hp1 HG01175.hp1 HG01361.hp1 others(13): Show |
intron_variant | MODIFIER | c.160+9417_160+9418d others(4): Show |
HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr11 | 43690361 | ||||||
| chr11:43690361 | CATAT | C | 17 | a0001c0001t0001g0030 a0001c0001t0001g0031 a0001c0001t0001g0050 others(14): Show |
17 | HG00738.hp2 HG01168.hp1 HG01258.hp2 others(14): Show |
intron_variant | MODIFIER | c.160+9415_160+9418d others(6): Show |
HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr11 | 43690361 | ||||||
| chr11:43690361 | CATATATA others(1): Show |
C | 6 | a0001c0001t0001g0199 a0001c0001t0001g0226 a0001c0001t0001g0262 others(3): Show |
6 | HG00140.hp1 HG02258.hp2 HG02280.hp1 others(3): Show |
intron_variant | MODIFIER | c.160+9411_160+9418d others(10): Show |
HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr11 | 43690361 | ||||||
| chr11:43690361 | CATATATA others(3): Show |
C | 3 | a0001c0001t0001g0220 a0001c0001t0001g0221 a0001c0003t0001g0225 |
3 | HG01167.hp2 HG01168.hp2 HG03834.hp2 |
intron_variant | MODIFIER | c.160+9409_160+9418d others(12): Show |
HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr11 | 43690361 | ||||||
| chr11:43690361 | CATATATA others(7): Show |
C | 2 | a0001c0001t0001g0115 a0002c0002t0002g0116 |
2 | NA19068.hp1 NA19084.hp1 |
intron_variant | MODIFIER | c.160+9405_160+9418d others(16): Show |
HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr11 | 43690361 | ||||||
| chr11:43690361 | CATATATA others(9): Show |
C | 3 | a0002c0002t0002g0175 a0002c0002t0002g0176 a0002c0002t0002g0177 |
3 | HG02647.hp1 HG02723.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.160+9403_160+9418d others(18): Show |
HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr11 | 43690361 | ||||||
| chr11:43690361 | CATATATA others(19): Show |
C | 2 | a0002c0002t0002g0178 a0002c0002t0002g0180 |
2 | HG01258.hp1 NA19010.hp2 |
intron_variant | MODIFIER | c.160+9393_160+9418d others(28): Show |
HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr11 | 43690361 | ||||||
| chr11:43690361 | CATATATA others(23): Show |
C | 1 | a0002c0002t0002g0181 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.160+9389_160+9418d others(32): Show |
HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr11 | 43690361 | ||||||
| chr11:43690365 | T | C | 1 | a0002c0002t0002g0201 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.160+9378T>C | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43690365 | |||||||
| chr11:43690379 | TATATATA others(2): Show |
T | 12 | a0001c0001t0001g0208 a0001c0001t0001g0209 a0001c0001t0001g0210 others(9): Show |
12 | HG01928.hp2 HG02523.hp2 HG02602.hp1 others(9): Show |
intron_variant | MODIFIER | c.160+9393_160+9401d others(11): Show |
HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43690379 | |||||||
| chr11:43690379 | TATATATA others(4): Show |
T | 1 | a0001c0001t0001g0254 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.160+9393_160+9403d others(13): Show |
HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43690379 | |||||||
| chr11:43690379 | TATATATA others(18): Show |
T | 1 | a0002c0002t0002g0179 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.160+9393_160+9417d others(27): Show |
HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43690379 | |||||||
| chr11:43690381 | TATATATA others(2): Show |
T | 4 | a0001c0001t0001g0217 a0001c0001t0001g0218 a0001c0001t0001g0219 others(1): Show |
4 | HG00099.hp2 HG01261.hp1 HG03704.hp2 others(1): Show |
intron_variant | MODIFIER | c.160+9395_160+9403d others(11): Show |
HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43690381 | |||||||
| chr11:43690383 | TATATATA others(14): Show |
T | 1 | a0002c0002t0002g0251 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.160+9397_160+9417d others(23): Show |
HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43690383 | |||||||
| chr11:43690384 | ATATATAT others(14): Show |
A | 3 | a0002c0002t0002g0250 a0002c0002t0002g0252 a0002c0002t0002g0253 |
3 | HG01891.hp1 HG02280.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.160+9399_160+9419d others(23): Show |
HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr11 | 43690384 | ||||||
| chr11:43690385 | T | C | 2 | a0001c0001t0001g0073 a0001c0001t0001g0081 |
2 | HG01975.hp2 HG02273.hp2 |
intron_variant | MODIFIER | c.160+9398T>C | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43690385 | |||||||
| chr11:43690386 | A | T | 1 | a0002c0002t0002g0167 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.160+9399A>T | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43690386 | |||||||
| chr11:43690386 | ATATATAT others(12): Show |
A | 2 | a0001c0001t0001g0111 a0001c0001t0001g0112 |
2 | HG02055.hp1 HG02809.hp2 |
intron_variant | MODIFIER | c.160+9401_160+9419d others(21): Show |
HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr11 | 43690386 | ||||||
| chr11:43690387 | T | C | 2 | a0001c0001t0001g0068 a0001c0001t0001g0085 |
2 | HG01175.hp1 HG01934.hp1 |
intron_variant | MODIFIER | c.160+9400T>C | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43690387 | |||||||
| chr11:43690387 | TA | T | 3 | a0001c0001t0001g0010 a0002c0002t0002g0190 a0002c0002t0002g0191 |
3 | HG02257.hp1 NA18982.hp2 NA19060.hp1 |
intron_variant | MODIFIER | c.160+9401delA | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43690387 | |||||||
| chr11:43690387 | TATA | T | 15 | a0001c0001t0001g0026 a0001c0001t0001g0046 a0001c0001t0001g0070 others(12): Show |
16 | HG00642.hp1 HG01069.hp2 HG01071.hp2 others(13): Show |
intron_variant | MODIFIER | c.160+9401_160+9403d others(5): Show |
HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43690387 | |||||||
| chr11:43690387 | TATATATA others(8): Show |
T | 1 | a0002c0002t0002g0161 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.160+9401_160+9415d others(17): Show |
HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43690387 | |||||||
| chr11:43690387 | TATATATA others(10): Show |
T | 1 | a0001c0001t0001g0036 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.160+9401_160+9417d others(19): Show |
HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43690387 | |||||||
| chr11:43690388 | A | AT | 10 | a0001c0001t0001g0129 a0001c0003t0001g0229 a0001c0003t0001g0237 others(7): Show |
10 | HG01361.hp2 HG02717.hp2 HG02738.hp1 others(7): Show |
intron_variant | MODIFIER | c.160+9402dupT | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr11 | 43690388 | ||||||
| chr11:43690388 | A | T | 11 | a0001c0001t0001g0006 a0001c0001t0001g0199 a0001c0003t0001g0272 others(8): Show |
11 | HG00140.hp1 HG00280.hp2 HG00423.hp1 others(8): Show |
intron_variant | MODIFIER | c.160+9401A>T | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43690388 | |||||||
| chr11:43690389 | TA | T | 3 | a0001c0001t0001g0061 a0001c0001t0001g0062 a0001c0007t0001g0230 |
3 | HG02258.hp1 HG03471.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.160+9403delA | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43690389 | |||||||
| chr11:43690389 | TATA | T | 23 | a0001c0001t0001g0028 a0001c0001t0001g0034 a0001c0001t0001g0035 others(20): Show |
23 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(20): Show |
intron_variant | MODIFIER | c.160+9403_160+9405d others(5): Show |
HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43690389 | |||||||
| chr11:43690390 | A | ATTTTTTT others(8): Show |
1 | a0001c0001t0001g0125 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.160+9404_160+9405i others(17): Show |
HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr11 | 43690390 | ||||||
| chr11:43690390 | A | T | 59 | a0001c0001t0001g0006 a0001c0001t0001g0010 a0001c0001t0001g0045 others(56): Show |
59 | HG00140.hp1 HG00280.hp2 HG00423.hp1 others(56): Show |
intron_variant | MODIFIER | c.160+9403A>T | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43690390 | |||||||
| chr11:43690391 | TA | T | 4 | a0001c0001t0001g0041 a0001c0001t0001g0042 a0001c0001t0001g0079 others(1): Show |
4 | HG00735.hp2 HG02300.hp2 NA18966.hp1 others(1): Show |
intron_variant | MODIFIER | c.160+9405delA | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43690391 | |||||||
| chr11:43690391 | TATA | T | 8 | a0001c0001t0001g0040 a0001c0001t0001g0043 a0001c0001t0001g0065 others(5): Show |
8 | HG01192.hp1 HG02083.hp2 HG02683.hp1 others(5): Show |
intron_variant | MODIFIER | c.160+9405_160+9407d others(5): Show |
HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43690391 | |||||||
| chr11:43690392 | A | ATT | 3 | a0001c0003t0001g0240 a0001c0003t0003g0231 a0001c0003t0003g0232 |
3 | HG02896.hp1 HG02897.hp1 HG03654.hp1 |
intron_variant | MODIFIER | c.160+9406_160+9407i others(4): Show |
HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr11 | 43690392 | ||||||
| chr11:43690392 | A | ATTTTTTT others(8): Show |
1 | a0001c0001t0001g0266 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.160+9406_160+9407i others(17): Show |
HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr11 | 43690392 | ||||||
| chr11:43690392 | A | T | 97 | a0001c0001t0001g0006 a0001c0001t0001g0010 a0001c0001t0001g0026 others(94): Show |
98 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(95): Show |
intron_variant | MODIFIER | c.160+9405A>T | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43690392 | |||||||
| chr11:43690394 | A | T | 138 | a0001c0001t0001g0006 a0001c0001t0001g0010 a0001c0001t0001g0026 others(135): Show |
139 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(136): Show |
intron_variant | MODIFIER | c.160+9407A>T | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43690394 | |||||||
| chr11:43690396 | A | ATTTTTTT others(4): Show |
1 | a0005c0006t0012g0021 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.160+9410_160+9411i others(13): Show |
HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr11 | 43690396 | ||||||
| chr11:43690396 | A | ATTTTTTT others(5): Show |
1 | a0001c0001t0003g0022 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.160+9410_160+9411i others(14): Show |
HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr11 | 43690396 | ||||||
| chr11:43690396 | A | T | 155 | a0001c0001t0001g0006 a0001c0001t0001g0010 a0001c0001t0001g0026 others(152): Show |
156 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(153): Show |
intron_variant | MODIFIER | c.160+9409A>T | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43690396 | |||||||
| chr11:43690398 | A | ATTTTTTT | 4 | a0001c0003t0003g0243 a0001c0003t0003g0246 a0001c0003t0003g0247 others(1): Show |
4 | HG01070.hp2 HG01071.hp1 HG03942.hp2 others(1): Show |
intron_variant | MODIFIER | c.160+9412_160+9413i others(9): Show |
HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr11 | 43690398 | ||||||
| chr11:43690398 | A | ATTTTTTT others(4): Show |
1 | a0001c0001t0001g0258 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.160+9412_160+9413i others(13): Show |
HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr11 | 43690398 | ||||||
| chr11:43690398 | A | ATTTTTTT others(5): Show |
5 | a0001c0001t0003g0017 a0001c0001t0003g0018 a0001c0001t0003g0019 others(2): Show |
5 | NA18747.hp1 NA18945.hp1 NA19005.hp1 others(2): Show |
intron_variant | MODIFIER | c.160+9412_160+9413i others(14): Show |
HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr11 | 43690398 | ||||||
| chr11:43690398 | A | ATTTTTTT others(6): Show |
1 | a0001c0001t0003g0067 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.160+9412_160+9413i others(15): Show |
HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr11 | 43690398 | ||||||
| chr11:43690398 | A | T | 168 | a0001c0001t0001g0006 a0001c0001t0001g0010 a0001c0001t0001g0026 others(165): Show |
169 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(166): Show |
intron_variant | MODIFIER | c.160+9411A>T | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43690398 | |||||||
| chr11:43690400 | A | ATTTTTTT others(4): Show |
1 | a0001c0001t0001g0007 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.160+9414_160+9415i others(13): Show |
HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr11 | 43690400 | ||||||
| chr11:43690400 | A | ATTTTTTT others(6): Show |
1 | a0001c0001t0003g0267 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.160+9414_160+9415i others(15): Show |
HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr11 | 43690400 | ||||||
| chr11:43690400 | A | ATTTTTTT others(7): Show |
1 | a0001c0001t0003g0015 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.160+9414_160+9415i others(16): Show |
HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr11 | 43690400 | ||||||
| chr11:43690400 | A | ATTTTTTT others(10): Show |
1 | a0001c0001t0001g0120 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.160+9414_160+9415i others(19): Show |
HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr11 | 43690400 | ||||||
| chr11:43690400 | A | ATTTTTTT others(11): Show |
4 | a0001c0001t0001g0002 a0001c0001t0001g0121 a0001c0001t0001g0122 others(1): Show |
4 | HG01109.hp1 HG01496.hp1 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.160+9414_160+9415i others(20): Show |
HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr11 | 43690400 | ||||||
| chr11:43690400 | A | ATTTTTTT others(15): Show |
1 | a0001c0001t0001g0257 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.160+9414_160+9415i others(24): Show |
HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr11 | 43690400 | ||||||
| chr11:43690400 | A | T | 183 | a0001c0001t0001g0006 a0001c0001t0001g0009 a0001c0001t0001g0010 others(180): Show |
184 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(181): Show |
intron_variant | MODIFIER | c.160+9413A>T | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43690400 | |||||||
| chr11:43690402 | A | ATTTTTTT others(5): Show |
1 | a0002c0002t0004g0274 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.160+9416_160+9417i others(14): Show |
HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr11 | 43690402 | ||||||
| chr11:43690402 | A | ATTTTTTT others(8): Show |
1 | a0002c0002t0004g0205 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.160+9416_160+9417i others(17): Show |
HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr11 | 43690402 | ||||||
| chr11:43690402 | A | ATTTTTTT others(9): Show |
2 | a0001c0001t0003g0016 a0002c0002t0002g0162 |
2 | HG02622.hp1 NA18964.hp2 |
intron_variant | MODIFIER | c.160+9416_160+9417i others(18): Show |
HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr11 | 43690402 | ||||||
| chr11:43690402 | A | ATTTTTTT others(13): Show |
1 | a0001c0001t0001g0124 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.160+9416_160+9417i others(22): Show |
HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr11 | 43690402 | ||||||
| chr11:43690402 | A | T | 198 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0007 others(195): Show |
200 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(197): Show |
intron_variant | MODIFIER | c.160+9415A>T | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43690402 | |||||||
| chr11:43690404 | A | ATATATAT others(18): Show |
1 | a0002c0002t0002g0201 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.160+9418_160+9419i others(27): Show |
HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr11 | 43690404 | ||||||
| chr11:43690404 | A | ATATATAT others(3): Show |
1 | a0002c0002t0006g0108 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.160+9418_160+9419i others(12): Show |
HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr11 | 43690404 | ||||||
| chr11:43690404 | A | ATATATTT others(11): Show |
1 | a0002c0002t0002g0142 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.160+9418_160+9419i others(20): Show |
HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr11 | 43690404 | ||||||
| chr11:43690404 | A | ATATATTT others(16): Show |
1 | a0002c0002t0002g0004 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.160+9418_160+9419i others(25): Show |
HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr11 | 43690404 | ||||||
| chr11:43690404 | A | ATATATTT others(25): Show |
1 | a0001c0001t0001g0265 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.160+9418_160+9419i others(34): Show |
HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr11 | 43690404 | ||||||
| chr11:43690404 | A | ATATTTTT others(8): Show |
1 | a0001c0001t0003g0013 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.160+9418_160+9419i others(17): Show |
HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr11 | 43690404 | ||||||
| chr11:43690404 | A | ATATTTTT others(9): Show |
1 | a0001c0001t0001g0260 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.160+9418_160+9419i others(18): Show |
HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr11 | 43690404 | ||||||
| chr11:43690404 | A | ATATTTTT others(10): Show |
1 | a0002c0002t0002g0144 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.160+9418_160+9419i others(19): Show |
HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr11 | 43690404 | ||||||
| chr11:43690404 | A | ATATTTTT others(11): Show |
2 | a0002c0002t0002g0145 a0002c0002t0007g0146 |
2 | HG01109.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.160+9418_160+9419i others(20): Show |
HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr11 | 43690404 | ||||||
| chr11:43690404 | A | ATATTTTT others(16): Show |
1 | a0001c0001t0001g0255 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.160+9418_160+9419i others(25): Show |
HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr11 | 43690404 | ||||||
| chr11:43690404 | A | ATTTTTTT others(8): Show |
2 | a0001c0001t0001g0005 a0001c0001t0001g0256 |
2 | HG03540.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.160+9420_160+9434d others(17): Show |
HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr11 | 43690404 | ||||||
| chr11:43690404 | A | ATTTTTTT others(9): Show |
5 | a0001c0001t0001g0152 a0001c0001t0001g0271 a0002c0002t0002g0153 others(2): Show |
5 | HG01884.hp1 HG02622.hp2 HG02717.hp1 others(2): Show |
intron_variant | MODIFIER | c.160+9419_160+9434d others(18): Show |
HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr11 | 43690404 | ||||||
| chr11:43690404 | A | ATTTTTTT others(10): Show |
3 | a0001c0001t0001g0270 a0002c0002t0002g0138 a0002c0002t0002g0156 |
3 | HG02257.hp2 HG02630.hp1 HG02630.hp2 |
intron_variant | MODIFIER | c.160+9418_160+9434d others(19): Show |
HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr11 | 43690404 | ||||||
| chr11:43690404 | A | ATTTTTTT others(11): Show |
1 | a0001c0001t0003g0014 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.160+9434_160+9435i others(20): Show |
HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr11 | 43690404 | ||||||
| chr11:43690404 | A | T | 217 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0007 others(214): Show |
219 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(216): Show |
intron_variant | MODIFIER | c.160+9417A>T | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43690404 | |||||||
| chr11:43690406 | T | A | 3 | a0002c0002t0002g0131 a0002c0002t0002g0136 a0002c0002t0002g0137 |
3 | NA18943.hp2 NA18952.hp2 NA18953.hp2 |
intron_variant | MODIFIER | c.160+9419T>A | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43690406 | |||||||
| chr11:43690840 | T | A | 112 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(109): Show |
112 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(109): Show |
intron_variant | MODIFIER | c.160+9853T>A | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43690840 | |||||||
| chr11:43690967 | T | C | 1 | a0002c0002t0002g0166 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.160+9980T>C | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43690967 | |||||||
| chr11:43691144 | A | C | 112 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(109): Show |
112 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(109): Show |
intron_variant | MODIFIER | c.160+10157A>C | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43691144 | |||||||
| chr11:43691447 | C | G | 1 | a0001c0001t0003g0023 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.160+10460C>G | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43691447 | |||||||
| chr11:43691556 | C | T | 22 | a0001c0001t0001g0199 a0001c0001t0001g0208 a0001c0001t0001g0209 others(19): Show |
22 | HG00099.hp2 HG00140.hp1 HG01167.hp2 others(19): Show |
intron_variant | MODIFIER | c.160+10569C>T | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43691556 | |||||||
| chr11:43691586 | C | A | 4 | a0001c0001t0003g0267 a0001c0001t0003g0268 a0001c0001t0003g0278 others(1): Show |
4 | HG02572.hp1 HG02965.hp2 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.160+10599C>A | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43691586 | |||||||
| chr11:43691637 | C | A | 1 | a0001c0001t0001g0071 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.160+10650C>A | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43691637 | |||||||
| chr11:43691689 | A | G | 1 | a0001c0001t0001g0071 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.160+10702A>G | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43691689 | |||||||
| chr11:43692080 | T | C | 5 | a0001c0001t0003g0267 a0001c0001t0003g0268 a0001c0001t0003g0278 others(2): Show |
5 | HG02572.hp1 HG02965.hp2 HG03209.hp1 others(2): Show |
intron_variant | MODIFIER | c.160+11093T>C | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43692080 | |||||||
| chr11:43692293 | C | T | 91 | a0001c0001t0001g0026 a0001c0001t0001g0028 a0001c0001t0001g0029 others(88): Show |
92 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(89): Show |
intron_variant | MODIFIER | c.160+11306C>T | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43692293 | |||||||
| chr11:43692439 | G | A | 112 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(109): Show |
112 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(109): Show |
intron_variant | MODIFIER | c.160+11452G>A | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43692439 | |||||||
| chr11:43692456 | A | T | 13 | a0001c0001t0003g0013 a0001c0001t0003g0014 a0001c0001t0003g0015 others(10): Show |
13 | HG00280.hp1 HG00609.hp2 NA18612.hp2 others(10): Show |
intron_variant | MODIFIER | c.160+11469A>T | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43692456 | |||||||
| chr11:43692853 | A | AG | 117 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(114): Show |
117 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(114): Show |
intron_variant | MODIFIER | c.160+11866_160+1186 others(5): Show |
HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43692853 | |||||||
| chr11:43692854 | T | A | 117 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(114): Show |
117 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(114): Show |
intron_variant | MODIFIER | c.160+11867T>A | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43692854 | |||||||
| chr11:43692951 | T | G | 1 | a0001c0001t0003g0206 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.160+11964T>G | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43692951 | |||||||
| chr11:43693120 | G | A | 1 | a0002c0002t0002g0201 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.160+12133G>A | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43693120 | |||||||
| chr11:43693218 | T | C | 91 | a0001c0001t0001g0026 a0001c0001t0001g0028 a0001c0001t0001g0029 others(88): Show |
92 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(89): Show |
intron_variant | MODIFIER | c.160+12231T>C | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43693218 | |||||||
| chr11:43693299 | A | T | 117 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(114): Show |
117 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(114): Show |
intron_variant | MODIFIER | c.160+12312A>T | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43693299 | |||||||
| chr11:43693502 | G | C | 2 | a0002c0002t0004g0205 a0002c0002t0004g0274 |
2 | HG02451.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.160+12515G>C | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43693502 | |||||||
| chr11:43693517 | T | C | 16 | a0001c0001t0001g0128 a0001c0001t0001g0129 a0001c0003t0001g0197 others(13): Show |
16 | HG00639.hp2 HG00642.hp2 HG01069.hp1 others(13): Show |
intron_variant | MODIFIER | c.160+12530T>C | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43693517 | |||||||
| chr11:43693622 | C | T | 1 | a0001c0001t0003g0020 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.160+12635C>T | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43693622 | |||||||
| chr11:43694721 | T | C | 2 | a0001c0001t0001g0128 a0001c0001t0001g0129 |
2 | HG02738.hp1 NA20905.hp1 |
intron_variant | MODIFIER | c.160+13734T>C | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43694721 | |||||||
| chr11:43694813 | G | GA | 16 | a0001c0001t0001g0002 a0001c0001t0001g0120 a0001c0001t0001g0121 others(13): Show |
17 | HG01109.hp1 HG01496.hp1 HG02258.hp2 others(14): Show |
intron_variant | MODIFIER | c.160+13834dupA | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr11 | 43694813 | ||||||
| chr11:43694923 | C | T | 266 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(263): Show |
268 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(265): Show |
intron_variant | MODIFIER | c.160+13936C>T | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43694923 | |||||||
| chr11:43695305 | G | A | 9 | a0002c0002t0002g0001 a0002c0002t0002g0025 a0002c0002t0002g0037 others(6): Show |
10 | HG00642.hp1 HG01069.hp2 HG01071.hp2 others(7): Show |
intron_variant | MODIFIER | c.160+14318G>A | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43695305 | |||||||
| chr11:43695397 | G | A | 3 | a0002c0002t0002g0187 a0002c0002t0002g0188 a0002c0002t0002g0189 |
3 | HG00140.hp2 HG01167.hp1 HG01346.hp1 |
intron_variant | MODIFIER | c.160+14410G>A | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43695397 | |||||||
| chr11:43695549 | G | A | 3 | a0002c0002t0002g0117 a0002c0002t0002g0118 a0002c0002t0002g0119 |
3 | HG00408.hp2 HG02135.hp1 NA19090.hp1 |
intron_variant | MODIFIER | c.160+14562G>A | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43695549 | |||||||
| chr11:43695586 | A | T | 1 | a0002c0002t0002g0038 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.160+14599A>T | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43695586 | |||||||
| chr11:43695601 | A | G | 2 | a0002c0002t0002g0178 a0002c0002t0002g0179 |
2 | NA18949.hp2 NA19010.hp2 |
intron_variant | MODIFIER | c.160+14614A>G | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43695601 | |||||||
| chr11:43695671 | G | GTCT | 94 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(91): Show |
94 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(91): Show |
intron_variant | MODIFIER | c.160+14704_160+1470 others(7): Show |
HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr11 | 43695671 | ||||||
| chr11:43695671 | G | GTCTTCT | 4 | a0001c0001t0001g0265 a0001c0001t0001g0266 a0001c0001t0001g0270 others(1): Show |
4 | HG02451.hp2 HG02630.hp1 HG02630.hp2 others(1): Show |
intron_variant | MODIFIER | c.160+14701_160+1470 others(10): Show |
HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr11 | 43695671 | ||||||
| chr11:43695691 | C | CTTG | 16 | a0001c0001t0001g0128 a0001c0001t0001g0129 a0001c0003t0001g0197 others(13): Show |
16 | HG00639.hp2 HG00642.hp2 HG01069.hp1 others(13): Show |
intron_variant | MODIFIER | c.160+14706_160+1470 others(7): Show |
HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr11 | 43695691 | ||||||
| chr11:43695725 | A | G | 33 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(30): Show |
33 | HG00639.hp2 HG00642.hp2 HG01069.hp1 others(30): Show |
intron_variant | MODIFIER | c.160+14738A>G | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43695725 | |||||||
| chr11:43695945 | G | A | 5 | a0001c0001t0003g0267 a0001c0001t0003g0268 a0001c0001t0003g0278 others(2): Show |
5 | HG02572.hp1 HG02965.hp2 HG03209.hp1 others(2): Show |
intron_variant | MODIFIER | c.160+14958G>A | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43695945 | |||||||
| chr11:43695978 | G | A | 91 | a0001c0001t0001g0026 a0001c0001t0001g0028 a0001c0001t0001g0029 others(88): Show |
92 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(89): Show |
intron_variant | MODIFIER | c.160+14991G>A | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43695978 | |||||||
| chr11:43696009 | C | T | 1 | a0001c0001t0001g0065 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.160+15022C>T | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43696009 | |||||||
| chr11:43696154 | C | T | 1 | a0003c0004t0001g0249 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.160+15167C>T | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43696154 | |||||||
| chr11:43696831 | C | G | 3 | a0001c0001t0001g0111 a0001c0001t0001g0112 a0001c0001t0003g0206 |
3 | HG02055.hp1 HG02809.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.160+15844C>G | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43696831 | |||||||
| chr11:43696893 | C | T | 76 | a0001c0001t0001g0152 a0001c0001t0001g0186 a0001c0001t0001g0265 others(73): Show |
76 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(73): Show |
intron_variant | MODIFIER | c.160+15906C>T | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43696893 | |||||||
| chr11:43696937 | C | T | 1 | a0001c0003t0001g0227 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.160+15950C>T | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43696937 | |||||||
| chr11:43696955 | G | T | 1 | a0002c0002t0002g0201 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.160+15968G>T | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43696955 | |||||||
| chr11:43696964 | G | A | 1 | a0002c0002t0002g0201 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.160+15977G>A | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43696964 | |||||||
| chr11:43697115 | G | A | 1 | a0002c0002t0002g0139 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.160+16128G>A | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43697115 | |||||||
| chr11:43697551 | C | T | 76 | a0001c0001t0001g0152 a0001c0001t0001g0186 a0001c0001t0001g0265 others(73): Show |
76 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(73): Show |
intron_variant | MODIFIER | c.160+16564C>T | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43697551 | |||||||
| chr11:43697558 | A | T | 1 | a0002c0002t0002g0201 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.160+16571A>T | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43697558 | |||||||
| chr11:43697708 | A | G | 3 | a0001c0001t0001g0111 a0001c0001t0001g0112 a0001c0001t0003g0206 |
3 | HG02055.hp1 HG02809.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.160+16721A>G | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43697708 | |||||||
| chr11:43698119 | G | A | 1 | a0001c0001t0001g0254 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.160+17132G>A | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43698119 | |||||||
| chr11:43698226 | A | G | 1 | a0001c0001t0001g0032 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.160+17239A>G | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43698226 | |||||||
| chr11:43698300 | C | T | 3 | a0001c0001t0001g0202 a0001c0001t0001g0203 a0001c0001t0001g0204 |
3 | HG02559.hp2 HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.160+17313C>T | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43698300 | |||||||
| chr11:43698448 | A | G | 3 | a0002c0002t0002g0131 a0002c0002t0002g0136 a0002c0002t0002g0137 |
3 | NA18943.hp2 NA18952.hp2 NA18953.hp2 |
intron_variant | MODIFIER | c.160+17461A>G | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43698448 | |||||||
| chr11:43698737 | T | C | 1 | a0001c0001t0001g0093 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.160+17750T>C | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43698737 | |||||||
| chr11:43698769 | T | G | 2 | a0001c0001t0001g0030 a0001c0001t0001g0031 |
2 | HG01168.hp1 HG01258.hp2 |
intron_variant | MODIFIER | c.160+17782T>G | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43698769 | |||||||
| chr11:43698800 | G | C | 117 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(114): Show |
117 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(114): Show |
intron_variant | MODIFIER | c.160+17813G>C | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43698800 | |||||||
| chr11:43698823 | A | C | 8 | a0001c0001t0001g0202 a0001c0001t0001g0203 a0001c0001t0001g0204 others(5): Show |
8 | HG02559.hp2 HG02572.hp1 HG02895.hp1 others(5): Show |
intron_variant | MODIFIER | c.160+17836A>C | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43698823 | |||||||
| chr11:43698882 | C | T | 1 | a0001c0001t0003g0023 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.160+17895C>T | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43698882 | |||||||
| chr11:43698883 | C | T | 3 | a0002c0002t0002g0163 a0002c0002t0002g0164 a0002c0002t0002g0183 |
3 | HG02080.hp2 HG02083.hp1 HG02165.hp1 |
intron_variant | MODIFIER | c.160+17896C>T | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43698883 | |||||||
| chr11:43699098 | G | T | 3 | a0002c0002t0002g0133 a0002c0002t0002g0134 a0002c0002t0002g0135 |
3 | HG02818.hp1 HG02886.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.160+18111G>T | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43699098 | |||||||
| chr11:43699216 | A | T | 1 | a0001c0001t0001g0068 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.160+18229A>T | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43699216 | |||||||
| chr11:43699307 | A | G | 3 | a0001c0001t0001g0033 a0001c0001t0001g0054 a0001c0001t0001g0125 |
3 | HG01884.hp2 HG02895.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.160+18320A>G | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43699307 | |||||||
| chr11:43699648 | G | C | 1 | a0001c0001t0001g0217 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.160+18661G>C | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43699648 | |||||||
| chr11:43699950 | T | C | 134 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(131): Show |
134 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(131): Show |
intron_variant | MODIFIER | c.160+18963T>C | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43699950 | |||||||
| chr11:43699999 | A | G | 2 | a0001c0003t0001g0225 a0001c0003t0001g0272 |
2 | HG00140.hp1 HG01167.hp2 |
intron_variant | MODIFIER | c.160+19012A>G | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43699999 | |||||||
| chr11:43700122 | C | A | 112 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(109): Show |
112 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(109): Show |
intron_variant | MODIFIER | c.160+19135C>A | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43700122 | |||||||
| chr11:43700288 | G | A | 1 | a0001c0001t0001g0073 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.160+19301G>A | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43700288 | |||||||
| chr11:43700327 | G | A | 3 | a0001c0001t0001g0202 a0001c0001t0001g0203 a0001c0001t0001g0204 |
3 | HG02559.hp2 HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.160+19340G>A | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43700327 | |||||||
| chr11:43700341 | C | T | 1 | a0002c0002t0002g0201 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.160+19354C>T | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43700341 | |||||||
| chr11:43700392 | C | T | 12 | a0001c0001t0003g0013 a0001c0001t0003g0014 a0001c0001t0003g0015 others(9): Show |
12 | HG00609.hp2 NA18612.hp2 NA18747.hp1 others(9): Show |
intron_variant | MODIFIER | c.160+19405C>T | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43700392 | |||||||
| chr11:43700503 | G | C | 2 | a0002c0002t0004g0205 a0002c0002t0004g0274 |
2 | HG02451.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.160+19516G>C | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43700503 | |||||||
| chr11:43700579 | C | G | 91 | a0001c0001t0001g0026 a0001c0001t0001g0028 a0001c0001t0001g0029 others(88): Show |
92 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(89): Show |
intron_variant | MODIFIER | c.160+19592C>G | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43700579 | |||||||
| chr11:43700631 | C | T | 109 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(106): Show |
109 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(106): Show |
intron_variant | MODIFIER | c.160+19644C>T | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43700631 | |||||||
| chr11:43700663 | A | T | 112 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(109): Show |
112 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(109): Show |
intron_variant | MODIFIER | c.160+19676A>T | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43700663 | |||||||
| chr11:43700739 | C | T | 109 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(106): Show |
109 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(106): Show |
intron_variant | MODIFIER | c.160+19752C>T | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43700739 | |||||||
| chr11:43700756 | T | C | 1 | a0001c0001t0001g0125 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.160+19769T>C | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43700756 | |||||||
| chr11:43700851 | A | G | 9 | a0001c0001t0001g0199 a0001c0001t0001g0209 a0001c0001t0001g0210 others(6): Show |
9 | HG01928.hp2 HG02523.hp2 NA18944.hp1 others(6): Show |
intron_variant | MODIFIER | c.160+19864A>G | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43700851 | |||||||
| chr11:43700892 | T | C | 3 | a0001c0001t0001g0033 a0001c0001t0001g0054 a0001c0001t0001g0125 |
3 | HG01884.hp2 HG02895.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.160+19905T>C | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43700892 | |||||||
| chr11:43700941 | C | T | 112 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(109): Show |
112 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(109): Show |
intron_variant | MODIFIER | c.160+19954C>T | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43700941 | |||||||
| chr11:43701355 | C | T | 1 | a0002c0002t0002g0151 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.160+20368C>T | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43701355 | |||||||
| chr11:43701366 | T | C | 3 | a0001c0001t0001g0033 a0001c0001t0001g0054 a0001c0001t0001g0125 |
3 | HG01884.hp2 HG02895.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.160+20379T>C | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43701366 | |||||||
| chr11:43701384 | G | T | 1 | a0002c0002t0002g0151 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.160+20397G>T | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43701384 | |||||||
| chr11:43701463 | T | C | 1 | a0001c0001t0003g0278 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.160+20476T>C | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43701463 | |||||||
| chr11:43701660 | G | T | 2 | a0002c0002t0002g0192 a0002c0002t0002g0194 |
2 | HG03516.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.160+20673G>T | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43701660 | |||||||
| chr11:43701665 | T | C | 1 | a0001c0001t0001g0074 | 1 | NA19085.hp2 | intron_variant | MODIFIER | c.160+20678T>C | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43701665 | |||||||
| chr11:43701717 | T | C | 1 | a0002c0002t0002g0201 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.160+20730T>C | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43701717 | |||||||
| chr11:43701867 | A | G | 1 | a0001c0001t0001g0009 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.160+20880A>G | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43701867 | |||||||
| chr11:43702082 | A | G | 117 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(114): Show |
117 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(114): Show |
intron_variant | MODIFIER | c.160+21095A>G | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43702082 | |||||||
| chr11:43702342 | G | C | 112 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(109): Show |
112 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(109): Show |
intron_variant | MODIFIER | c.160+21355G>C | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43702342 | |||||||
| chr11:43702440 | G | A | 227 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(224): Show |
228 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(225): Show |
intron_variant | MODIFIER | c.160+21453G>A | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43702440 | |||||||
| chr11:43702510 | G | A | 227 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(224): Show |
228 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(225): Show |
intron_variant | MODIFIER | c.160+21523G>A | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43702510 | |||||||
| chr11:43702590 | A | T | 3 | a0001c0001t0001g0202 a0001c0001t0001g0203 a0001c0001t0001g0204 |
3 | HG02559.hp2 HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.160+21603A>T | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43702590 | |||||||
| chr11:43702618 | G | A | 112 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(109): Show |
112 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(109): Show |
intron_variant | MODIFIER | c.160+21631G>A | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43702618 | |||||||
| chr11:43702713 | A | G | 1 | a0001c0001t0001g0087 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.160+21726A>G | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43702713 | |||||||
| chr11:43702916 | C | T | 112 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(109): Show |
112 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(109): Show |
intron_variant | MODIFIER | c.160+21929C>T | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43702916 | |||||||
| chr11:43702998 | A | G | 1 | a0002c0002t0002g0201 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.160+22011A>G | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43702998 | |||||||
| chr11:43703263 | T | C | 112 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(109): Show |
112 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(109): Show |
intron_variant | MODIFIER | c.160+22276T>C | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43703263 | |||||||
| chr11:43703267 | T | G | 1 | a0001c0003t0001g0229 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.160+22280T>G | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43703267 | |||||||
| chr11:43703296 | G | A | 1 | a0001c0001t0001g0088 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.160+22309G>A | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43703296 | |||||||
| chr11:43703330 | G | A | 1 | a0002c0002t0002g0117 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.160+22343G>A | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43703330 | |||||||
| chr11:43703430 | G | A | 13 | a0001c0001t0003g0013 a0001c0001t0003g0014 a0001c0001t0003g0015 others(10): Show |
13 | HG00280.hp1 HG00609.hp2 NA18612.hp2 others(10): Show |
intron_variant | MODIFIER | c.160+22443G>A | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43703430 | |||||||
| chr11:43703437 | G | A | 1 | a0002c0002t0005g0207 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.160+22450G>A | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43703437 | |||||||
| chr11:43703484 | G | A | 17 | a0002c0002t0002g0127 a0002c0002t0002g0140 a0002c0002t0002g0147 others(14): Show |
17 | HG00140.hp2 HG00323.hp1 HG00735.hp1 others(14): Show |
intron_variant | MODIFIER | c.160+22497G>A | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43703484 | |||||||
| chr11:43703549 | G | C | 5 | a0001c0001t0001g0209 a0001c0001t0001g0210 a0001c0001t0001g0211 others(2): Show |
5 | NA18966.hp2 NA18971.hp1 NA18973.hp1 others(2): Show |
intron_variant | MODIFIER | c.160+22562G>C | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43703549 | |||||||
| chr11:43703816 | G | T | 1 | a0002c0002t0009g0200 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.160+22829G>T | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43703816 | |||||||
| chr11:43703975 | G | A | 4 | a0002c0002t0002g0131 a0002c0002t0002g0136 a0002c0002t0002g0137 others(1): Show |
4 | NA18943.hp2 NA18952.hp2 NA18953.hp2 others(1): Show |
intron_variant | MODIFIER | c.160+22988G>A | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43703975 | |||||||
| chr11:43704069 | C | T | 112 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(109): Show |
112 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(109): Show |
intron_variant | MODIFIER | c.160+23082C>T | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43704069 | |||||||
| chr11:43704209 | G | A | 4 | a0001c0001t0001g0060 a0001c0001t0001g0061 a0001c0001t0001g0062 others(1): Show |
4 | HG02300.hp2 HG03453.hp2 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.160+23222G>A | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43704209 | |||||||
| chr11:43704661 | G | A | 22 | a0001c0001t0001g0199 a0001c0001t0001g0208 a0001c0001t0001g0209 others(19): Show |
22 | HG00099.hp2 HG00140.hp1 HG01167.hp2 others(19): Show |
intron_variant | MODIFIER | c.160+23674G>A | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43704661 | |||||||
| chr11:43704908 | C | A | 1 | a0001c0001t0001g0152 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.160+23921C>A | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43704908 | |||||||
| chr11:43705013 | G | A | 1 | a0001c0001t0001g0094 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.160+24026G>A | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43705013 | |||||||
| chr11:43705089 | A | G | 1 | a0001c0001t0003g0206 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.160+24102A>G | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43705089 | |||||||
| chr11:43705315 | T | C | 5 | a0001c0001t0003g0267 a0001c0001t0003g0268 a0001c0001t0003g0278 others(2): Show |
5 | HG02572.hp1 HG02965.hp2 HG03209.hp1 others(2): Show |
intron_variant | MODIFIER | c.160+24328T>C | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43705315 | |||||||
| chr11:43705568 | T | G | 2 | a0001c0001t0001g0034 a0001c0001t0001g0071 |
2 | NA18945.hp2 NA18982.hp1 |
intron_variant | MODIFIER | c.160+24581T>G | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43705568 | |||||||
| chr11:43705751 | CCT | C | 97 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(94): Show |
97 | HG00140.hp2 HG00280.hp2 HG00408.hp2 others(94): Show |
intron_variant | MODIFIER | c.160+24770_160+2477 others(6): Show |
HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr11 | 43705751 | ||||||
| chr11:43705753 | TCTCTC | T | 7 | a0001c0001t0001g0265 a0001c0001t0001g0266 a0001c0001t0001g0270 others(4): Show |
7 | HG02451.hp2 HG02572.hp1 HG02630.hp1 others(4): Show |
intron_variant | MODIFIER | c.160+24771_160+2477 others(9): Show |
HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr11 | 43705753 | ||||||
| chr11:43705756 | CTCCT | C | 9 | a0001c0003t0001g0238 a0001c0003t0003g0232 a0002c0002t0002g0127 others(6): Show |
9 | HG00323.hp1 HG00609.hp1 HG01070.hp1 others(6): Show |
intron_variant | MODIFIER | c.160+24770_160+2477 others(8): Show |
HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43705756 | |||||||
| chr11:43705759 | C | T | 1 | a0002c0002t0002g0135 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.160+24772C>T | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43705759 | |||||||
| chr11:43705760 | TC | T | 85 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(82): Show |
85 | HG00140.hp2 HG00280.hp2 HG00408.hp2 others(82): Show |
intron_variant | MODIFIER | c.160+24774delC | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43705760 | |||||||
| chr11:43705761 | C | T | 13 | a0001c0001t0001g0129 a0001c0001t0001g0186 a0002c0002t0002g0109 others(10): Show |
13 | HG00423.hp1 HG01175.hp2 HG01258.hp1 others(10): Show |
intron_variant | MODIFIER | c.160+24774C>T | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43705761 | |||||||
| chr11:43705761 | CT | C | 21 | a0001c0001t0001g0199 a0001c0001t0001g0208 a0001c0001t0001g0209 others(18): Show |
21 | HG00099.hp2 HG01167.hp2 HG01261.hp1 others(18): Show |
intron_variant | MODIFIER | c.160+24799delT | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr11 | 43705761 | ||||||
| chr11:43705761 | CTT | C | 23 | a0001c0001t0001g0046 a0001c0001t0001g0092 a0001c0001t0001g0111 others(20): Show |
23 | HG00140.hp1 HG00280.hp1 HG01168.hp2 others(20): Show |
intron_variant | MODIFIER | c.160+24798_160+2479 others(6): Show |
HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr11 | 43705761 | ||||||
| chr11:43705761 | CTTT | C | 86 | a0001c0001t0001g0026 a0001c0001t0001g0028 a0001c0001t0001g0029 others(83): Show |
87 | HG00099.hp1 HG00408.hp1 HG00423.hp2 others(84): Show |
intron_variant | MODIFIER | c.160+24797_160+2479 others(7): Show |
HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr11 | 43705761 | ||||||
| chr11:43705761 | CTTTT | C | 5 | a0001c0001t0001g0050 a0001c0001t0001g0055 a0001c0001t0001g0075 others(2): Show |
5 | HG00323.hp2 HG03239.hp1 NA18941.hp2 others(2): Show |
intron_variant | MODIFIER | c.160+24796_160+2479 others(8): Show |
HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr11 | 43705761 | ||||||
| chr11:43705762 | T | C | 7 | a0001c0001t0001g0265 a0001c0001t0001g0266 a0001c0001t0001g0270 others(4): Show |
7 | HG02451.hp2 HG02572.hp1 HG02630.hp1 others(4): Show |
intron_variant | MODIFIER | c.160+24775T>C | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43705762 | |||||||
| chr11:43705851 | T | G | 1 | a0002c0002t0002g0175 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.160+24864T>G | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43705851 | |||||||
| chr11:43705861 | A | T | 1 | a0002c0002t0002g0110 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.160+24874A>T | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43705861 | |||||||
| chr11:43705950 | A | C | 2 | a0002c0002t0004g0205 a0002c0002t0004g0274 |
2 | HG02451.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.160+24963A>C | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43705950 | |||||||
| chr11:43706026 | C | T | 1 | a0001c0001t0001g0095 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.160+25039C>T | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43706026 | |||||||
| chr11:43706027 | G | A | 117 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(114): Show |
117 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(114): Show |
intron_variant | MODIFIER | c.160+25040G>A | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43706027 | |||||||
| chr11:43706191 | GTTTATC | G | 10 | a0001c0001t0001g0128 a0001c0001t0001g0129 a0001c0003t0001g0197 others(7): Show |
10 | HG00639.hp2 HG01069.hp1 HG01106.hp1 others(7): Show |
intron_variant | MODIFIER | c.160+25209_160+2521 others(10): Show |
HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr11 | 43706191 | ||||||
| chr11:43706436 | T | G | 266 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(263): Show |
268 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(265): Show |
intron_variant | MODIFIER | c.160+25449T>G | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43706436 | |||||||
| chr11:43706522 | A | C | 1 | a0001c0001t0001g0113 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.160+25535A>C | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43706522 | |||||||
| chr11:43706661 | TAGTC | T | 10 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(7): Show |
10 | HG01261.hp2 HG02257.hp1 HG02258.hp1 others(7): Show |
intron_variant | MODIFIER | c.160+25676_160+2567 others(8): Show |
HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr11 | 43706661 | ||||||
| chr11:43706689 | G | GGT | 22 | a0001c0001t0001g0029 a0001c0001t0001g0036 a0001c0001t0001g0051 others(19): Show |
22 | HG00609.hp2 HG02004.hp2 HG02135.hp2 others(19): Show |
intron_variant | MODIFIER | c.160+25733_160+2573 others(6): Show |
HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr11 | 43706689 | ||||||
| chr11:43706689 | G | GGTGT | 5 | a0001c0001t0001g0254 a0001c0001t0001g0255 a0001c0001t0003g0023 others(2): Show |
5 | HG00280.hp1 HG02922.hp1 HG03209.hp2 others(2): Show |
intron_variant | MODIFIER | c.160+25731_160+2573 others(8): Show |
HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr11 | 43706689 | ||||||
| chr11:43706689 | G | GGTGTGTG others(1): Show |
8 | a0001c0001t0001g0005 a0001c0001t0001g0265 a0001c0001t0001g0266 others(5): Show |
8 | HG02451.hp2 HG02572.hp1 HG02630.hp1 others(5): Show |
intron_variant | MODIFIER | c.160+25727_160+2573 others(12): Show |
HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr11 | 43706689 | ||||||
| chr11:43706689 | G | GGTGTGTG others(3): Show |
16 | a0001c0001t0001g0128 a0001c0001t0001g0129 a0001c0003t0001g0198 others(13): Show |
16 | HG00639.hp2 HG00642.hp2 HG01069.hp1 others(13): Show |
intron_variant | MODIFIER | c.160+25725_160+2573 others(14): Show |
HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr11 | 43706689 | ||||||
| chr11:43706689 | G | GGTGTGTG others(5): Show |
57 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0009 others(54): Show |
57 | HG00140.hp2 HG00280.hp2 HG00423.hp1 others(54): Show |
intron_variant | MODIFIER | c.160+25723_160+2573 others(16): Show |
HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr11 | 43706689 | ||||||
| chr11:43706689 | G | GGTGTGTG others(7): Show |
13 | a0001c0001t0001g0152 a0001c0003t0001g0229 a0002c0002t0002g0117 others(10): Show |
13 | HG00609.hp1 HG01175.hp2 HG02080.hp2 others(10): Show |
intron_variant | MODIFIER | c.160+25721_160+2573 others(18): Show |
HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr11 | 43706689 | ||||||
| chr11:43706689 | G | GGTGTGTG others(9): Show |
10 | a0001c0001t0001g0006 a0001c0003t0003g0242 a0001c0003t0003g0245 others(7): Show |
10 | HG00323.hp1 HG00408.hp2 HG01070.hp2 others(7): Show |
intron_variant | MODIFIER | c.160+25719_160+2573 others(20): Show |
HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr11 | 43706689 | ||||||
| chr11:43706689 | G | GGTGTGTG others(11): Show |
5 | a0001c0003t0003g0231 a0001c0003t0003g0232 a0001c0003t0003g0243 others(2): Show |
5 | HG02004.hp1 HG02155.hp2 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.160+25717_160+2573 others(22): Show |
HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr11 | 43706689 | ||||||
| chr11:43706689 | G | GGTGTGTG others(15): Show |
1 | a0001c0003t0003g0246 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.160+25713_160+2573 others(26): Show |
HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr11 | 43706689 | ||||||
| chr11:43706721 | T | TGTGTGTG others(2): Show |
4 | a0002c0002t0002g0161 a0002c0002t0002g0175 a0002c0002t0002g0176 others(1): Show |
4 | HG02647.hp1 HG02723.hp1 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.160+25734_160+2573 others(13): Show |
HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43706721 | |||||||
| chr11:43706721 | T | TGTGTGTG others(6): Show |
1 | a0001c0003t0001g0240 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.160+25734_160+2573 others(17): Show |
HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43706721 | |||||||
| chr11:43706724 | T | TTG | 4 | a0002c0002t0002g0161 a0002c0002t0002g0175 a0002c0002t0002g0176 others(1): Show |
4 | HG02647.hp1 HG02723.hp1 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.160+25737_160+2573 others(6): Show |
HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43706724 | |||||||
| chr11:43706780 | T | C | 91 | a0001c0001t0001g0026 a0001c0001t0001g0028 a0001c0001t0001g0029 others(88): Show |
92 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(89): Show |
intron_variant | MODIFIER | c.160+25793T>C | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43706780 | |||||||
| chr11:43706834 | T | G | 1 | a0002c0002t0002g0201 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.160+25847T>G | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43706834 | |||||||
| chr11:43706944 | T | C | 3 | a0001c0001t0001g0111 a0001c0001t0001g0112 a0001c0001t0003g0206 |
3 | HG02055.hp1 HG02809.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.160+25957T>C | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43706944 | |||||||
| chr11:43706984 | A | T | 73 | a0001c0001t0001g0152 a0001c0001t0001g0186 a0002c0002t0002g0004 others(70): Show |
73 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(70): Show |
intron_variant | MODIFIER | c.160+25997A>T | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43706984 | |||||||
| chr11:43707161 | G | A | 7 | a0002c0002t0002g0132 a0002c0002t0002g0166 a0002c0002t0002g0167 others(4): Show |
7 | HG00280.hp2 HG00738.hp1 HG01099.hp1 others(4): Show |
intron_variant | MODIFIER | c.160+26174G>A | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43707161 | |||||||
| chr11:43707180 | T | C | 227 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(224): Show |
228 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(225): Show |
intron_variant | MODIFIER | c.160+26193T>C | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43707180 | |||||||
| chr11:43707446 | C | T | 2 | a0002c0002t0002g0178 a0002c0002t0002g0179 |
2 | NA18949.hp2 NA19010.hp2 |
intron_variant | MODIFIER | c.160+26459C>T | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43707446 | |||||||
| chr11:43707606 | C | A | 1 | a0001c0001t0001g0152 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.160+26619C>A | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43707606 | |||||||
| chr11:43707955 | A | G | 1 | a0002c0002t0002g0109 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.160+26968A>G | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43707955 | |||||||
| chr11:43708292 | AAAC | A | 16 | a0001c0001t0001g0111 a0001c0001t0001g0112 a0001c0001t0003g0013 others(13): Show |
16 | HG00280.hp1 HG00609.hp2 HG02055.hp1 others(13): Show |
intron_variant | MODIFIER | c.160+27311_160+2731 others(7): Show |
HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr11 | 43708292 | ||||||
| chr11:43708303 | G | A | 73 | a0001c0001t0001g0152 a0001c0001t0001g0186 a0002c0002t0002g0004 others(70): Show |
73 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(70): Show |
intron_variant | MODIFIER | c.160+27316G>A | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43708303 | |||||||
| chr11:43708437 | A | G | 73 | a0001c0001t0001g0152 a0001c0001t0001g0186 a0002c0002t0002g0004 others(70): Show |
73 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(70): Show |
intron_variant | MODIFIER | c.160+27450A>G | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43708437 | |||||||
| chr11:43708905 | G | A | 117 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(114): Show |
117 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(114): Show |
intron_variant | MODIFIER | c.160+27918G>A | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43708905 | |||||||
| chr11:43709045 | C | G | 1 | a0001c0001t0001g0271 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.160+28058C>G | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43709045 | |||||||
| chr11:43709195 | G | T | 117 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(114): Show |
117 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(114): Show |
intron_variant | MODIFIER | c.160+28208G>T | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43709195 | |||||||
| chr11:43709270 | C | T | 1 | a0001c0001t0001g0053 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.160+28283C>T | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43709270 | |||||||
| chr11:43709369 | G | A | 1 | a0001c0001t0001g0032 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.160+28382G>A | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43709369 | |||||||
| chr11:43709676 | T | A | 1 | a0001c0001t0001g0030 | 1 | HG01258.hp2 | intron_variant | MODIFIER | c.160+28689T>A | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43709676 | |||||||
| chr11:43709677 | G | A | 1 | a0001c0001t0001g0030 | 1 | HG01258.hp2 | intron_variant | MODIFIER | c.160+28690G>A | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43709677 | |||||||
| chr11:43709901 | G | A | 117 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(114): Show |
117 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(114): Show |
intron_variant | MODIFIER | c.160+28914G>A | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43709901 | |||||||
| chr11:43709949 | C | G | 1 | a0001c0001t0001g0029 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.160+28962C>G | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43709949 | |||||||
| chr11:43709970 | G | C | 1 | a0001c0001t0001g0050 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.160+28983G>C | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43709970 | |||||||
| chr11:43710257 | G | A | 1 | a0001c0001t0001g0050 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.160+29270G>A | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43710257 | |||||||
| chr11:43710520 | G | A | 10 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(7): Show |
10 | HG01261.hp2 HG02257.hp1 HG02258.hp1 others(7): Show |
intron_variant | MODIFIER | c.160+29533G>A | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43710520 | |||||||
| chr11:43710678 | T | C | 1 | a0002c0002t0002g0142 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.160+29691T>C | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43710678 | |||||||
| chr11:43710794 | T | A | 3 | a0001c0001t0001g0202 a0001c0001t0001g0203 a0001c0001t0001g0204 |
3 | HG02559.hp2 HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.160+29807T>A | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43710794 | |||||||
| chr11:43710885 | G | A | 1 | a0001c0001t0001g0226 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.160+29898G>A | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43710885 | |||||||
| chr11:43710913 | T | C | 117 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(114): Show |
117 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(114): Show |
intron_variant | MODIFIER | c.160+29926T>C | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43710913 | |||||||
| chr11:43711032 | A | G | 1 | a0001c0001t0001g0213 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.160+30045A>G | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43711032 | |||||||
| chr11:43711314 | ATATT | A | 4 | a0001c0003t0003g0243 a0001c0003t0003g0246 a0001c0003t0003g0247 others(1): Show |
4 | HG01070.hp2 HG01071.hp1 HG03942.hp2 others(1): Show |
intron_variant | MODIFIER | c.160+30333_160+3033 others(8): Show |
HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr11 | 43711314 | ||||||
| chr11:43711474 | G | GT | 8 | a0001c0001t0001g0045 a0001c0001t0001g0186 a0001c0001t0001g0263 others(5): Show |
8 | HG01891.hp2 HG02258.hp2 HG02976.hp1 others(5): Show |
intron_variant | MODIFIER | c.160+30505dupT | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr11 | 43711474 | ||||||
| chr11:43711474 | GT | G | 7 | a0001c0001t0001g0076 a0001c0001t0003g0267 a0001c0001t0003g0268 others(4): Show |
7 | HG01167.hp2 HG02572.hp1 HG02896.hp1 others(4): Show |
intron_variant | MODIFIER | c.160+30505delT | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr11 | 43711474 | ||||||
| chr11:43711543 | C | T | 4 | a0001c0003t0001g0197 a0001c0003t0001g0198 a0001c0003t0001g0237 others(1): Show |
4 | HG01361.hp2 HG03654.hp1 HG03669.hp2 others(1): Show |
intron_variant | MODIFIER | c.160+30556C>T | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43711543 | |||||||
| chr11:43711567 | C | T | 23 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(20): Show |
23 | HG00642.hp2 HG01070.hp2 HG01071.hp1 others(20): Show |
intron_variant | MODIFIER | c.160+30580C>T | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43711567 | |||||||
| chr11:43711568 | G | A | 2 | a0002c0002t0002g0126 a0002c0002t0002g0182 |
2 | NA18964.hp1 NA19000.hp1 |
intron_variant | MODIFIER | c.160+30581G>A | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43711568 | |||||||
| chr11:43711771 | G | A | 3 | a0001c0001t0001g0202 a0001c0001t0001g0203 a0001c0001t0001g0204 |
3 | HG02559.hp2 HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.160+30784G>A | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43711771 | |||||||
| chr11:43711819 | G | A | 1 | a0002c0002t0002g0176 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.160+30832G>A | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43711819 | |||||||
| chr11:43712056 | A | G | 1 | a0001c0001t0001g0083 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.160+31069A>G | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43712056 | |||||||
| chr11:43712060 | C | T | 4 | a0001c0001t0001g0256 a0001c0001t0001g0257 a0001c0001t0001g0258 others(1): Show |
4 | HG02896.hp2 HG02922.hp2 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.160+31073C>T | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43712060 | |||||||
| chr11:43712083 | A | G | 3 | a0001c0001t0001g0202 a0001c0001t0001g0203 a0001c0001t0001g0204 |
3 | HG02559.hp2 HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.160+31096A>G | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43712083 | |||||||
| chr11:43712200 | G | A | 2 | a0001c0001t0001g0006 a0001c0001t0001g0010 |
2 | HG02257.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.160+31213G>A | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43712200 | |||||||
| chr11:43712296 | A | G | 22 | a0001c0001t0001g0199 a0001c0001t0001g0208 a0001c0001t0001g0209 others(19): Show |
22 | HG00099.hp2 HG00140.hp1 HG01167.hp2 others(19): Show |
intron_variant | MODIFIER | c.160+31309A>G | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43712296 | |||||||
| chr11:43712310 | C | A | 2 | a0002c0002t0004g0205 a0002c0002t0004g0274 |
2 | HG02451.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.160+31323C>A | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43712310 | |||||||
| chr11:43712351 | A | G | 5 | a0001c0001t0001g0032 a0001c0001t0001g0202 a0001c0001t0001g0203 others(2): Show |
5 | HG02559.hp2 HG02895.hp1 HG02897.hp2 others(2): Show |
intron_variant | MODIFIER | c.160+31364A>G | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43712351 | |||||||
| chr11:43712404 | C | T | 13 | a0001c0001t0003g0013 a0001c0001t0003g0014 a0001c0001t0003g0015 others(10): Show |
13 | HG00280.hp1 HG00609.hp2 NA18612.hp2 others(10): Show |
intron_variant | MODIFIER | c.160+31417C>T | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43712404 | |||||||
| chr11:43712620 | G | A | 1 | a0002c0002t0002g0162 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.160+31633G>A | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43712620 | |||||||
| chr11:43712653 | T | C | 1 | a0002c0002t0002g0201 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.160+31666T>C | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43712653 | |||||||
| chr11:43712678 | C | A | 1 | a0003c0004t0001g0241 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.160+31691C>A | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43712678 | |||||||
| chr11:43712711 | T | C | 249 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(246): Show |
250 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(247): Show |
intron_variant | MODIFIER | c.160+31724T>C | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43712711 | |||||||
| chr11:43712712 | G | A | 1 | a0002c0002t0002g0201 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.160+31725G>A | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43712712 | |||||||
| chr11:43712727 | G | A | 2 | a0001c0003t0003g0231 a0001c0003t0003g0232 |
2 | HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.160+31740G>A | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43712727 | |||||||
| chr11:43712994 | A | G | 1 | a0002c0002t0002g0175 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.160+32007A>G | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43712994 | |||||||
| chr11:43713132 | T | A | 4 | a0001c0001t0001g0006 a0001c0001t0001g0010 a0002c0002t0002g0201 others(1): Show |
4 | HG02257.hp1 HG03098.hp1 NA18522.hp1 others(1): Show |
intron_variant | MODIFIER | c.160+32145T>A | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43713132 | |||||||
| chr11:43713279 | T | TC | 27 | a0001c0001t0001g0032 a0001c0001t0001g0046 a0001c0001t0001g0048 others(24): Show |
27 | HG00642.hp1 HG00738.hp1 HG01106.hp1 others(24): Show |
intron_variant | MODIFIER | c.160+32298dupC | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr11 | 43713279 | ||||||
| chr11:43713582 | T | G | 5 | a0002c0002t0002g0131 a0002c0002t0002g0136 a0002c0002t0002g0137 others(2): Show |
5 | NA18943.hp2 NA18952.hp2 NA18953.hp2 others(2): Show |
intron_variant | MODIFIER | c.160+32595T>G | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43713582 | |||||||
| chr11:43713591 | G | A | 2 | a0002c0002t0002g0161 a0002c0002t0002g0176 |
2 | HG03130.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.160+32604G>A | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43713591 | |||||||
| chr11:43713653 | A | G | 227 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(224): Show |
228 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(225): Show |
intron_variant | MODIFIER | c.160+32666A>G | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43713653 | |||||||
| chr11:43713677 | T | A | 4 | a0002c0002t0002g0117 a0002c0002t0002g0118 a0002c0002t0002g0119 others(1): Show |
4 | HG00408.hp2 HG02135.hp1 NA19084.hp2 others(1): Show |
intron_variant | MODIFIER | c.160+32690T>A | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43713677 | |||||||
| chr11:43713697 | G | A | 4 | a0001c0003t0001g0197 a0001c0003t0001g0198 a0001c0003t0001g0237 others(1): Show |
4 | HG01361.hp2 HG03654.hp1 HG03669.hp2 others(1): Show |
intron_variant | MODIFIER | c.160+32710G>A | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43713697 | |||||||
| chr11:43713734 | G | A | 2 | a0001c0003t0003g0231 a0001c0003t0003g0232 |
2 | HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.160+32747G>A | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43713734 | |||||||
| chr11:43713762 | A | G | 1 | a0001c0001t0001g0152 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.160+32775A>G | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43713762 | |||||||
| chr11:43714129 | T | G | 1 | a0002c0002t0002g0201 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.160+33142T>G | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43714129 | |||||||
| chr11:43714151 | G | T | 3 | a0001c0001t0001g0202 a0001c0001t0001g0203 a0001c0001t0001g0204 |
3 | HG02559.hp2 HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.160+33164G>T | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43714151 | |||||||
| chr11:43714191 | C | T | 1 | a0001c0001t0003g0013 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.160+33204C>T | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43714191 | |||||||
| chr11:43714197 | C | G | 35 | a0001c0001t0001g0186 a0002c0002t0002g0004 a0002c0002t0002g0109 others(32): Show |
35 | HG00280.hp2 HG00423.hp1 HG00738.hp1 others(32): Show |
intron_variant | MODIFIER | c.160+33210C>G | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43714197 | |||||||
| chr11:43714223 | C | T | 13 | a0001c0001t0003g0013 a0001c0001t0003g0014 a0001c0001t0003g0015 others(10): Show |
13 | HG00280.hp1 HG00609.hp2 NA18612.hp2 others(10): Show |
intron_variant | MODIFIER | c.160+33236C>T | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43714223 | |||||||
| chr11:43714528 | C | T | 3 | a0001c0001t0001g0202 a0001c0001t0001g0203 a0001c0001t0001g0204 |
3 | HG02559.hp2 HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.160+33541C>T | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43714528 | |||||||
| chr11:43714599 | T | C | 118 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(115): Show |
118 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(115): Show |
intron_variant | MODIFIER | c.160+33612T>C | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43714599 | |||||||
| chr11:43714874 | C | A | 1 | a0002c0002t0002g0201 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.160+33887C>A | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43714874 | |||||||
| chr11:43714996 | T | G | 16 | a0001c0001t0001g0002 a0001c0001t0001g0120 a0001c0001t0001g0121 others(13): Show |
17 | HG01109.hp1 HG01496.hp1 HG02258.hp2 others(14): Show |
intron_variant | MODIFIER | c.160+34009T>G | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43714996 | |||||||
| chr11:43715069 | G | A | 3 | a0001c0001t0001g0202 a0001c0001t0001g0203 a0001c0001t0001g0204 |
3 | HG02559.hp2 HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.160+34082G>A | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43715069 | |||||||
| chr11:43715140 | C | T | 1 | a0002c0002t0002g0201 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.160+34153C>T | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43715140 | |||||||
| chr11:43715303 | A | G | 3 | a0001c0001t0001g0202 a0001c0001t0001g0203 a0001c0001t0001g0204 |
3 | HG02559.hp2 HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.160+34316A>G | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43715303 | |||||||
| chr11:43715472 | A | G | 1 | a0002c0002t0002g0182 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.160+34485A>G | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43715472 | |||||||
| chr11:43715535 | T | C | 1 | a0001c0001t0001g0260 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.160+34548T>C | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43715535 | |||||||
| chr11:43715549 | G | T | 1 | a0001c0001t0001g0226 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.160+34562G>T | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43715549 | |||||||
| chr11:43715555 | A | G | 3 | a0001c0001t0001g0044 a0001c0001t0001g0051 a0001c0001t0001g0052 |
3 | HG01516.hp2 HG02004.hp2 HG02055.hp2 |
intron_variant | MODIFIER | c.160+34568A>G | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43715555 | |||||||
| chr11:43715566 | A | G | 118 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(115): Show |
118 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(115): Show |
intron_variant | MODIFIER | c.160+34579A>G | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43715566 | |||||||
| chr11:43715584 | C | A | 1 | a0001c0001t0001g0096 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.160+34597C>A | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43715584 | |||||||
| chr11:43715674 | T | G | 37 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(34): Show |
37 | HG00639.hp2 HG00642.hp2 HG01069.hp1 others(34): Show |
intron_variant | MODIFIER | c.160+34687T>G | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43715674 | |||||||
| chr11:43715794 | C | T | 2 | a0001c0001t0001g0186 a0001c0001t0003g0023 |
2 | HG00280.hp1 HG01891.hp2 |
intron_variant | MODIFIER | c.160+34807C>T | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43715794 | |||||||
| chr11:43715803 | T | G | 1 | a0001c0007t0001g0230 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.160+34816T>G | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43715803 | |||||||
| chr11:43715880 | C | T | 249 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(246): Show |
250 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(247): Show |
intron_variant | MODIFIER | c.160+34893C>T | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43715880 | |||||||
| chr11:43715898 | G | A | 2 | a0001c0001t0001g0006 a0001c0001t0001g0010 |
2 | HG02257.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.160+34911G>A | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43715898 | |||||||
| chr11:43715920 | G | A | 2 | a0002c0002t0004g0205 a0002c0002t0004g0274 |
2 | HG02451.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.160+34933G>A | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43715920 | |||||||
| chr11:43715951 | G | A | 1 | a0001c0001t0001g0032 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.161-34960G>A | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43715951 | |||||||
| chr11:43716326 | A | G | 3 | a0001c0001t0001g0202 a0001c0001t0001g0203 a0001c0001t0001g0204 |
3 | HG02559.hp2 HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.161-34585A>G | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43716326 | |||||||
| chr11:43716450 | A | G | 1 | a0001c0001t0001g0031 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.161-34461A>G | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43716450 | |||||||
| chr11:43716470 | G | A | 2 | a0001c0003t0003g0244 a0001c0003t0003g0245 |
2 | HG02004.hp1 HG03239.hp2 |
intron_variant | MODIFIER | c.161-34441G>A | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43716470 | |||||||
| chr11:43716505 | T | C | 1 | a0002c0002t0002g0039 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.161-34406T>C | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43716505 | |||||||
| chr11:43716563 | G | A | 13 | a0001c0001t0003g0013 a0001c0001t0003g0014 a0001c0001t0003g0015 others(10): Show |
13 | HG00280.hp1 HG00609.hp2 NA18612.hp2 others(10): Show |
intron_variant | MODIFIER | c.161-34348G>A | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43716563 | |||||||
| chr11:43716742 | C | CAT | 22 | a0001c0001t0001g0199 a0001c0001t0001g0208 a0001c0001t0001g0209 others(19): Show |
22 | HG00099.hp2 HG00140.hp1 HG01167.hp2 others(19): Show |
intron_variant | MODIFIER | c.161-34155_161-3415 others(6): Show |
HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr11 | 43716742 | ||||||
| chr11:43716742 | CAT | C | 23 | a0002c0002t0002g0127 a0002c0002t0002g0139 a0002c0002t0002g0140 others(20): Show |
23 | HG00140.hp2 HG00323.hp1 HG00639.hp1 others(20): Show |
intron_variant | MODIFIER | c.161-34155_161-3415 others(6): Show |
HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr11 | 43716742 | ||||||
| chr11:43716803 | T | C | 1 | a0001c0001t0001g0152 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.161-34108T>C | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43716803 | |||||||
| chr11:43717091 | AG | A | 3 | a0001c0001t0001g0111 a0001c0001t0001g0112 a0001c0001t0003g0206 |
3 | HG02055.hp1 HG02809.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.161-33819delG | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43717091 | |||||||
| chr11:43717248 | T | C | 2 | a0002c0002t0004g0205 a0002c0002t0004g0274 |
2 | HG02451.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.161-33663T>C | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43717248 | |||||||
| chr11:43717397 | A | G | 3 | a0001c0001t0001g0045 a0001c0001t0001g0082 a0001c0001t0001g0086 |
3 | HG02165.hp2 HG03831.hp1 NA19060.hp2 |
intron_variant | MODIFIER | c.161-33514A>G | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43717397 | |||||||
| chr11:43717547 | T | G | 1 | a0001c0001t0001g0097 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.161-33364T>G | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43717547 | |||||||
| chr11:43717646 | C | T | 4 | a0001c0001t0003g0267 a0001c0001t0003g0268 a0001c0001t0003g0278 others(1): Show |
4 | HG02572.hp1 HG02965.hp2 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.161-33265C>T | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43717646 | |||||||
| chr11:43717804 | C | CT | 33 | a0001c0001t0001g0070 a0001c0001t0001g0077 a0001c0001t0001g0078 others(30): Show |
33 | HG00642.hp2 HG01069.hp1 HG01070.hp2 others(30): Show |
intron_variant | MODIFIER | c.161-33089dupT | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr11 | 43717804 | ||||||
| chr11:43717804 | CT | C | 76 | a0001c0001t0001g0152 a0001c0001t0001g0186 a0001c0001t0001g0195 others(73): Show |
76 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(73): Show |
intron_variant | MODIFIER | c.161-33089delT | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr11 | 43717804 | ||||||
| chr11:43717804 | CTT | C | 9 | a0001c0001t0001g0265 a0001c0001t0001g0266 a0001c0001t0001g0270 others(6): Show |
9 | HG01515.hp2 HG02451.hp2 HG02572.hp1 others(6): Show |
intron_variant | MODIFIER | c.161-33090_161-3308 others(6): Show |
HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr11 | 43717804 | ||||||
| chr11:43717886 | C | T | 1 | a0001c0001t0001g0046 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.161-33025C>T | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43717886 | |||||||
| chr11:43717927 | C | A | 4 | a0002c0002t0002g0117 a0002c0002t0002g0118 a0002c0002t0002g0119 others(1): Show |
4 | HG00408.hp2 HG02135.hp1 NA19084.hp2 others(1): Show |
intron_variant | MODIFIER | c.161-32984C>A | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43717927 | |||||||
| chr11:43718051 | C | T | 1 | a0001c0001t0001g0062 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.161-32860C>T | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43718051 | |||||||
| chr11:43718101 | G | A | 1 | a0002c0002t0009g0200 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.161-32810G>A | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43718101 | |||||||
| chr11:43718307 | G | A | 78 | a0001c0001t0001g0026 a0001c0001t0001g0028 a0001c0001t0001g0029 others(75): Show |
79 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(76): Show |
intron_variant | MODIFIER | c.161-32604G>A | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43718307 | |||||||
| chr11:43718353 | G | C | 3 | a0001c0001t0001g0033 a0001c0001t0001g0054 a0001c0001t0001g0125 |
3 | HG01884.hp2 HG02895.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.161-32558G>C | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43718353 | |||||||
| chr11:43718715 | A | G | 3 | a0001c0001t0001g0202 a0001c0001t0001g0203 a0001c0001t0001g0204 |
3 | HG02559.hp2 HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.161-32196A>G | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43718715 | |||||||
| chr11:43718723 | A | G | 3 | a0002c0002t0002g0251 a0002c0002t0002g0252 a0002c0002t0002g0253 |
3 | HG01891.hp1 HG06807.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.161-32188A>G | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43718723 | |||||||
| chr11:43718832 | C | T | 5 | a0001c0001t0003g0267 a0001c0001t0003g0268 a0001c0001t0003g0278 others(2): Show |
5 | HG02572.hp1 HG02965.hp2 HG03209.hp1 others(2): Show |
intron_variant | MODIFIER | c.161-32079C>T | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43718832 | |||||||
| chr11:43718839 | G | A | 1 | a0002c0002t0008g0003 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.161-32072G>A | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43718839 | |||||||
| chr11:43718872 | T | C | 227 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(224): Show |
228 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(225): Show |
intron_variant | MODIFIER | c.161-32039T>C | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43718872 | |||||||
| chr11:43718990 | C | A | 1 | a0002c0002t0002g0201 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.161-31921C>A | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43718990 | |||||||
| chr11:43719615 | CA | C | 12 | a0001c0001t0001g0254 a0001c0001t0003g0267 a0001c0001t0003g0268 others(9): Show |
12 | HG01070.hp1 HG02451.hp1 HG02572.hp1 others(9): Show |
intron_variant | MODIFIER | c.161-31283delA | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr11 | 43719615 | ||||||
| chr11:43719615 | CAA | C | 16 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(13): Show |
16 | HG01261.hp2 HG01891.hp2 HG02257.hp1 others(13): Show |
intron_variant | MODIFIER | c.161-31284_161-3128 others(6): Show |
HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr11 | 43719615 | ||||||
| chr11:43719625 | A | AT | 4 | a0001c0001t0001g0104 a0001c0001t0001g0202 a0001c0001t0001g0203 others(1): Show |
4 | HG02559.hp2 HG02895.hp1 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.161-31286_161-3128 others(5): Show |
HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43719625 | |||||||
| chr11:43719625 | A | T | 1 | a0001c0001t0001g0226 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.161-31286A>T | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43719625 | |||||||
| chr11:43719626 | AAAT | A | 19 | a0001c0001t0001g0128 a0001c0001t0001g0129 a0001c0003t0001g0197 others(16): Show |
19 | HG00423.hp1 HG00639.hp2 HG00642.hp2 others(16): Show |
intron_variant | MODIFIER | c.161-31283_161-3128 others(7): Show |
HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr11 | 43719626 | ||||||
| chr11:43719627 | A | AT | 23 | a0001c0001t0001g0046 a0001c0001t0001g0063 a0001c0001t0001g0069 others(20): Show |
23 | HG00280.hp1 HG00609.hp2 HG01515.hp1 others(20): Show |
intron_variant | MODIFIER | c.161-31284_161-3128 others(5): Show |
HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43719627 | |||||||
| chr11:43719627 | A | T | 57 | a0001c0001t0001g0026 a0001c0001t0001g0032 a0001c0001t0001g0033 others(54): Show |
57 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(54): Show |
intron_variant | MODIFIER | c.161-31284A>T | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43719627 | |||||||
| chr11:43719627 | AAT | A | 61 | a0001c0001t0001g0152 a0001c0003t0001g0229 a0001c0003t0003g0231 others(58): Show |
61 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(58): Show |
intron_variant | MODIFIER | c.161-31268_161-3126 others(6): Show |
HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr11 | 43719627 | ||||||
| chr11:43719629 | T | A | 6 | a0001c0001t0001g0057 a0001c0001t0001g0124 a0002c0002t0002g0001 others(3): Show |
7 | HG00642.hp1 HG01069.hp2 HG01071.hp2 others(4): Show |
intron_variant | MODIFIER | c.161-31282T>A | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43719629 | |||||||
| chr11:43719631 | T | A | 4 | a0002c0002t0002g0161 a0002c0002t0002g0176 a0002c0002t0002g0177 others(1): Show |
4 | HG02572.hp2 HG02723.hp1 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.161-31280T>A | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43719631 | |||||||
| chr11:43719947 | G | A | 2 | a0002c0002t0004g0205 a0002c0002t0004g0274 |
2 | HG02451.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.161-30964G>A | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43719947 | |||||||
| chr11:43719980 | T | C | 1 | a0001c0001t0001g0026 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.161-30931T>C | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43719980 | |||||||
| chr11:43720106 | ATCTTATG others(8): Show |
A | 3 | a0001c0001t0001g0111 a0001c0001t0001g0112 a0001c0001t0003g0206 |
3 | HG02055.hp1 HG02809.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.161-30801_161-3078 others(19): Show |
HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr11 | 43720106 | ||||||
| chr11:43720145 | A | G | 34 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(31): Show |
34 | HG00639.hp2 HG00642.hp2 HG01069.hp1 others(31): Show |
intron_variant | MODIFIER | c.161-30766A>G | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43720145 | |||||||
| chr11:43720170 | G | A | 1 | a0002c0002t0008g0003 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.161-30741G>A | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43720170 | |||||||
| chr11:43720262 | T | C | 266 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(263): Show |
268 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(265): Show |
intron_variant | MODIFIER | c.161-30649T>C | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43720262 | |||||||
| chr11:43720391 | G | T | 34 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(31): Show |
34 | HG00639.hp2 HG00642.hp2 HG01069.hp1 others(31): Show |
intron_variant | MODIFIER | c.161-30520G>T | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43720391 | |||||||
| chr11:43720616 | G | A | 1 | a0001c0001t0001g0218 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.161-30295G>A | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43720616 | |||||||
| chr11:43720806 | G | A | 1 | a0002c0002t0002g0201 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.161-30105G>A | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43720806 | |||||||
| chr11:43720816 | TA | T | 115 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(112): Show |
115 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(112): Show |
intron_variant | MODIFIER | c.161-30094delA | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43720816 | |||||||
| chr11:43720849 | A | G | 1 | a0001c0001t0001g0271 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.161-30062A>G | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43720849 | |||||||
| chr11:43720851 | A | C | 1 | a0002c0002t0002g0175 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.161-30060A>C | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43720851 | |||||||
| chr11:43720927 | A | T | 118 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(115): Show |
118 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(115): Show |
intron_variant | MODIFIER | c.161-29984A>T | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43720927 | |||||||
| chr11:43721197 | G | C | 1 | a0001c0001t0001g0087 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.161-29714G>C | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43721197 | |||||||
| chr11:43721280 | C | G | 1 | a0001c0003t0001g0272 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.161-29631C>G | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43721280 | |||||||
| chr11:43721280 | C | T | 115 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(112): Show |
115 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(112): Show |
intron_variant | MODIFIER | c.161-29631C>T | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43721280 | |||||||
| chr11:43721347 | C | T | 1 | a0001c0001t0001g0226 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.161-29564C>T | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43721347 | |||||||
| chr11:43721573 | C | T | 4 | a0001c0001t0003g0267 a0001c0001t0003g0268 a0001c0001t0003g0278 others(1): Show |
4 | HG02572.hp1 HG02965.hp2 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.161-29338C>T | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43721573 | |||||||
| chr11:43721752 | T | C | 121 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(118): Show |
121 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(118): Show |
intron_variant | MODIFIER | c.161-29159T>C | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43721752 | |||||||
| chr11:43721834 | G | T | 3 | a0001c0001t0001g0202 a0001c0001t0001g0203 a0001c0001t0001g0204 |
3 | HG02559.hp2 HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.161-29077G>T | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43721834 | |||||||
| chr11:43721857 | C | T | 3 | a0001c0001t0001g0202 a0001c0001t0001g0203 a0001c0001t0001g0204 |
3 | HG02559.hp2 HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.161-29054C>T | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43721857 | |||||||
| chr11:43721948 | A | G | 1 | a0001c0001t0001g0032 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.161-28963A>G | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43721948 | |||||||
| chr11:43722136 | C | G | 8 | a0002c0002t0002g0004 a0002c0002t0002g0144 a0002c0002t0002g0145 others(5): Show |
8 | HG01884.hp1 HG02622.hp1 HG02630.hp2 others(5): Show |
intron_variant | MODIFIER | c.161-28775C>G | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43722136 | |||||||
| chr11:43722229 | A | G | 1 | a0001c0001t0001g0028 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.161-28682A>G | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43722229 | |||||||
| chr11:43722452 | C | A | 3 | a0001c0001t0001g0033 a0001c0001t0001g0054 a0001c0001t0001g0125 |
3 | HG01884.hp2 HG02895.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.161-28459C>A | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43722452 | |||||||
| chr11:43722608 | A | T | 2 | a0001c0001t0001g0051 a0001c0001t0001g0052 |
2 | HG02004.hp2 HG02055.hp2 |
intron_variant | MODIFIER | c.161-28303A>T | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43722608 | |||||||
| chr11:43722771 | C | T | 1 | a0001c0001t0001g0271 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.161-28140C>T | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43722771 | |||||||
| chr11:43722773 | C | T | 1 | a0002c0002t0002g0165 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.161-28138C>T | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43722773 | |||||||
| chr11:43722797 | C | T | 2 | a0002c0002t0002g0138 a0002c0002t0007g0146 |
2 | HG01109.hp2 HG02257.hp2 |
intron_variant | MODIFIER | c.161-28114C>T | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43722797 | |||||||
| chr11:43722833 | G | GA | 234 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(231): Show |
236 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(233): Show |
intron_variant | MODIFIER | c.161-28068dupA | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr11 | 43722833 | ||||||
| chr11:43722966 | C | T | 2 | a0002c0002t0002g0163 a0002c0002t0002g0164 |
2 | HG02083.hp1 HG02165.hp1 |
intron_variant | MODIFIER | c.161-27945C>T | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43722966 | |||||||
| chr11:43722982 | G | T | 3 | a0001c0001t0001g0265 a0001c0001t0001g0266 a0001c0001t0001g0270 |
3 | HG02451.hp2 HG02630.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.161-27929G>T | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43722982 | |||||||
| chr11:43722997 | A | T | 2 | a0001c0001t0003g0020 a0005c0006t0012g0021 |
2 | HG00609.hp2 NA19070.hp1 |
intron_variant | MODIFIER | c.161-27914A>T | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43722997 | |||||||
| chr11:43723346 | G | C | 2 | a0002c0002t0002g0150 a0002c0002t0002g0160 |
2 | HG00609.hp1 HG02155.hp2 |
intron_variant | MODIFIER | c.161-27565G>C | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43723346 | |||||||
| chr11:43723574 | T | C | 2 | a0002c0002t0004g0205 a0002c0002t0004g0274 |
2 | HG02451.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.161-27337T>C | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43723574 | |||||||
| chr11:43723615 | A | G | 1 | a0001c0001t0001g0047 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.161-27296A>G | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43723615 | |||||||
| chr11:43723617 | G | A | 4 | a0001c0001t0001g0060 a0001c0001t0001g0061 a0001c0001t0001g0062 others(1): Show |
4 | HG02300.hp2 HG03453.hp2 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.161-27294G>A | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43723617 | |||||||
| chr11:43723906 | C | T | 1 | a0001c0001t0001g0026 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.161-27005C>T | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43723906 | |||||||
| chr11:43723962 | AT | A | 123 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(120): Show |
124 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(121): Show |
intron_variant | MODIFIER | c.161-26938delT | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr11 | 43723962 | ||||||
| chr11:43724014 | A | G | 90 | a0001c0001t0001g0026 a0001c0001t0001g0028 a0001c0001t0001g0029 others(87): Show |
91 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(88): Show |
intron_variant | MODIFIER | c.161-26897A>G | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43724014 | |||||||
| chr11:43724025 | A | C | 1 | a0002c0002t0009g0200 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.161-26886A>C | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43724025 | |||||||
| chr11:43724042 | C | T | 1 | a0001c0001t0001g0271 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.161-26869C>T | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43724042 | |||||||
| chr11:43724057 | G | A | 3 | a0001c0001t0001g0111 a0001c0001t0001g0112 a0001c0001t0003g0206 |
3 | HG02055.hp1 HG02809.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.161-26854G>A | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43724057 | |||||||
| chr11:43724219 | C | CTG | 70 | a0001c0001t0001g0033 a0001c0001t0001g0045 a0001c0001t0001g0046 others(67): Show |
70 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(67): Show |
intron_variant | MODIFIER | c.161-26652_161-2665 others(6): Show |
HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr11 | 43724219 | ||||||
| chr11:43724219 | C | CTGTG | 41 | a0001c0001t0001g0010 a0001c0001t0001g0032 a0001c0001t0001g0060 others(38): Show |
41 | HG00140.hp2 HG00408.hp2 HG00609.hp2 others(38): Show |
intron_variant | MODIFIER | c.161-26654_161-2665 others(8): Show |
HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr11 | 43724219 | ||||||
| chr11:43724219 | C | CTGTGTG | 15 | a0001c0001t0001g0063 a0001c0001t0001g0115 a0001c0001t0001g0219 others(12): Show |
15 | HG00642.hp2 HG01070.hp2 HG01071.hp1 others(12): Show |
intron_variant | MODIFIER | c.161-26656_161-2665 others(10): Show |
HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr11 | 43724219 | ||||||
| chr11:43724219 | C | CTGTGTGT others(3): Show |
3 | a0001c0003t0001g0234 a0001c0003t0001g0236 a0002c0002t0002g0158 |
3 | HG00639.hp2 HG01106.hp1 HG02698.hp1 |
intron_variant | MODIFIER | c.161-26660_161-2665 others(14): Show |
HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr11 | 43724219 | ||||||
| chr11:43724219 | CTG | C | 14 | a0001c0001t0001g0008 a0001c0001t0001g0209 a0001c0001t0001g0210 others(11): Show |
14 | HG01099.hp2 HG01106.hp2 HG01258.hp1 others(11): Show |
intron_variant | MODIFIER | c.161-26652_161-2665 others(6): Show |
HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr11 | 43724219 | ||||||
| chr11:43724219 | CTGTG | C | 7 | a0001c0001t0001g0043 a0001c0001t0001g0079 a0001c0001t0001g0080 others(4): Show |
7 | HG00423.hp2 HG01123.hp1 HG02451.hp2 others(4): Show |
intron_variant | MODIFIER | c.161-26654_161-2665 others(8): Show |
HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr11 | 43724219 | ||||||
| chr11:43724219 | CTGTGTGT others(1): Show |
C | 3 | a0001c0001t0001g0203 a0001c0001t0001g0204 a0001c0003t0003g0243 |
3 | HG02895.hp1 HG02897.hp2 HG03942.hp2 |
intron_variant | MODIFIER | c.161-26658_161-2665 others(12): Show |
HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr11 | 43724219 | ||||||
| chr11:43724219 | CTGTGTGT others(3): Show |
C | 1 | a0001c0001t0001g0202 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.161-26660_161-2665 others(14): Show |
HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr11 | 43724219 | ||||||
| chr11:43724219 | CTGTGTGT others(7): Show |
C | 2 | a0002c0002t0004g0205 a0002c0002t0004g0274 |
2 | HG02451.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.161-26664_161-2665 others(18): Show |
HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr11 | 43724219 | ||||||
| chr11:43724245 | G | C | 1 | a0002c0002t0002g0201 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.161-26666G>C | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43724245 | |||||||
| chr11:43724260 | T | TGTGTGTG others(4): Show |
1 | a0002c0002t0002g0039 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.161-26651_161-2665 others(15): Show |
HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43724260 | |||||||
| chr11:43724492 | G | A | 1 | a0002c0002t0002g0165 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.161-26419G>A | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43724492 | |||||||
| chr11:43724526 | AC | A | 3 | a0001c0001t0001g0202 a0001c0001t0001g0203 a0001c0001t0001g0204 |
3 | HG02559.hp2 HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.161-26384delC | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43724526 | |||||||
| chr11:43724541 | A | G | 1 | a0001c0001t0001g0010 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.161-26370A>G | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43724541 | |||||||
| chr11:43724685 | C | T | 1 | a0002c0002t0002g0201 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.161-26226C>T | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43724685 | |||||||
| chr11:43724699 | T | C | 3 | a0001c0001t0001g0202 a0001c0001t0001g0203 a0001c0001t0001g0204 |
3 | HG02559.hp2 HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.161-26212T>C | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43724699 | |||||||
| chr11:43724759 | A | G | 3 | a0001c0001t0001g0217 a0001c0001t0001g0218 a0001c0001t0001g0220 |
3 | HG00099.hp2 HG01168.hp2 HG01261.hp1 |
intron_variant | MODIFIER | c.161-26152A>G | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43724759 | |||||||
| chr11:43724988 | C | T | 1 | a0002c0002t0002g0117 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.161-25923C>T | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43724988 | |||||||
| chr11:43725044 | A | G | 91 | a0001c0001t0001g0026 a0001c0001t0001g0028 a0001c0001t0001g0029 others(88): Show |
92 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(89): Show |
intron_variant | MODIFIER | c.161-25867A>G | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43725044 | |||||||
| chr11:43725330 | G | A | 1 | a0001c0001t0001g0099 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.161-25581G>A | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43725330 | |||||||
| chr11:43725352 | T | G | 9 | a0001c0001t0003g0014 a0001c0001t0003g0015 a0001c0001t0003g0016 others(6): Show |
9 | NA18612.hp2 NA18747.hp1 NA18945.hp1 others(6): Show |
intron_variant | MODIFIER | c.161-25559T>G | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43725352 | |||||||
| chr11:43725845 | G | A | 2 | a0001c0001t0001g0203 a0001c0001t0001g0204 |
2 | HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.161-25066G>A | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43725845 | |||||||
| chr11:43725854 | G | A | 1 | a0001c0001t0001g0032 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.161-25057G>A | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43725854 | |||||||
| chr11:43725882 | G | A | 1 | a0001c0001t0001g0075 | 1 | NA18949.hp1 | intron_variant | MODIFIER | c.161-25029G>A | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43725882 | |||||||
| chr11:43726004 | A | T | 17 | a0001c0001t0001g0111 a0001c0001t0001g0112 a0001c0001t0003g0013 others(14): Show |
17 | HG00280.hp1 HG00609.hp2 HG02055.hp1 others(14): Show |
intron_variant | MODIFIER | c.161-24907A>T | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43726004 | |||||||
| chr11:43726165 | T | G | 4 | a0002c0002t0002g0250 a0002c0002t0002g0251 a0002c0002t0002g0252 others(1): Show |
4 | HG01891.hp1 HG02280.hp2 HG06807.hp2 others(1): Show |
intron_variant | MODIFIER | c.161-24746T>G | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43726165 | |||||||
| chr11:43726250 | G | A | 124 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(121): Show |
125 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(122): Show |
intron_variant | MODIFIER | c.161-24661G>A | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43726250 | |||||||
| chr11:43726362 | A | G | 82 | a0001c0001t0001g0002 a0001c0001t0001g0120 a0001c0001t0001g0121 others(79): Show |
83 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(80): Show |
intron_variant | MODIFIER | c.161-24549A>G | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43726362 | |||||||
| chr11:43726445 | A | T | 2 | a0002c0002t0004g0205 a0002c0002t0004g0274 |
2 | HG02451.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.161-24466A>T | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43726445 | |||||||
| chr11:43726560 | T | C | 3 | a0001c0001t0001g0202 a0001c0001t0001g0203 a0001c0001t0001g0204 |
3 | HG02559.hp2 HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.161-24351T>C | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43726560 | |||||||
| chr11:43726734 | T | C | 12 | a0001c0001t0003g0013 a0001c0001t0003g0014 a0001c0001t0003g0015 others(9): Show |
12 | HG00609.hp2 NA18612.hp2 NA18747.hp1 others(9): Show |
intron_variant | MODIFIER | c.161-24177T>C | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43726734 | |||||||
| chr11:43726835 | A | G | 2 | a0001c0001t0001g0088 a0001c0001t0001g0091 |
2 | HG00738.hp2 HG02738.hp2 |
intron_variant | MODIFIER | c.161-24076A>G | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43726835 | |||||||
| chr11:43726879 | A | G | 1 | a0002c0002t0008g0003 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.161-24032A>G | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43726879 | |||||||
| chr11:43727033 | T | C | 3 | a0001c0003t0003g0231 a0001c0003t0003g0232 a0002c0002t0002g0155 |
3 | HG01884.hp1 HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.161-23878T>C | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43727033 | |||||||
| chr11:43727069 | A | G | 14 | a0001c0001t0003g0267 a0001c0001t0003g0268 a0001c0001t0003g0278 others(11): Show |
14 | HG01070.hp2 HG01071.hp1 HG01884.hp1 others(11): Show |
intron_variant | MODIFIER | c.161-23842A>G | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43727069 | |||||||
| chr11:43727123 | C | T | 128 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(125): Show |
128 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(125): Show |
intron_variant | MODIFIER | c.161-23788C>T | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43727123 | |||||||
| chr11:43727203 | C | T | 3 | a0001c0001t0001g0111 a0001c0001t0003g0206 a0003c0004t0001g0249 |
3 | HG02055.hp1 HG03579.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.161-23708C>T | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43727203 | |||||||
| chr11:43727210 | T | C | 1 | a0001c0001t0001g0074 | 1 | NA19085.hp2 | intron_variant | MODIFIER | c.161-23701T>C | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43727210 | |||||||
| chr11:43727490 | CT | C | 231 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(228): Show |
233 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(230): Show |
intron_variant | MODIFIER | c.161-23409delT | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr11 | 43727490 | ||||||
| chr11:43727569 | C | T | 1 | a0001c0001t0001g0208 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.161-23342C>T | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43727569 | |||||||
| chr11:43727589 | G | T | 1 | a0002c0002t0009g0200 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.161-23322G>T | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43727589 | |||||||
| chr11:43727649 | A | G | 110 | a0001c0001t0001g0026 a0001c0001t0001g0028 a0001c0001t0001g0029 others(107): Show |
110 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(107): Show |
intron_variant | MODIFIER | c.161-23262A>G | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43727649 | |||||||
| chr11:43728022 | A | C | 3 | a0001c0001t0001g0202 a0001c0001t0001g0203 a0001c0001t0001g0204 |
3 | HG02559.hp2 HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.161-22889A>C | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43728022 | |||||||
| chr11:43728038 | T | A | 52 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(49): Show |
52 | HG00099.hp2 HG00140.hp1 HG00639.hp2 others(49): Show |
intron_variant | MODIFIER | c.161-22873T>A | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43728038 | |||||||
| chr11:43728222 | C | T | 18 | a0001c0001t0001g0111 a0001c0001t0001g0112 a0001c0001t0003g0013 others(15): Show |
18 | HG00280.hp1 HG00609.hp2 HG02055.hp1 others(15): Show |
intron_variant | MODIFIER | c.161-22689C>T | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43728222 | |||||||
| chr11:43728348 | A | T | 14 | a0001c0001t0003g0013 a0001c0001t0003g0014 a0001c0001t0003g0015 others(11): Show |
14 | HG00280.hp1 HG00609.hp2 NA18612.hp2 others(11): Show |
intron_variant | MODIFIER | c.161-22563A>T | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43728348 | |||||||
| chr11:43728402 | T | A | 1 | a0001c0001t0001g0070 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.161-22509T>A | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43728402 | |||||||
| chr11:43728450 | T | C | 1 | a0001c0001t0003g0023 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.161-22461T>C | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43728450 | |||||||
| chr11:43728476 | T | TA | 18 | a0001c0001t0001g0111 a0001c0001t0001g0112 a0001c0001t0003g0013 others(15): Show |
18 | HG00280.hp1 HG00609.hp2 HG02055.hp1 others(15): Show |
intron_variant | MODIFIER | c.161-22425dupA | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr11 | 43728476 | ||||||
| chr11:43728533 | C | A | 1 | a0001c0001t0001g0054 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.161-22378C>A | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43728533 | |||||||
| chr11:43728718 | C | T | 6 | a0002c0002t0002g0004 a0002c0002t0002g0145 a0002c0002t0002g0153 others(3): Show |
6 | HG02622.hp1 HG02630.hp2 HG02717.hp1 others(3): Show |
intron_variant | MODIFIER | c.161-22193C>T | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43728718 | |||||||
| chr11:43728826 | G | A | 6 | a0001c0003t0001g0197 a0001c0003t0001g0198 a0001c0003t0001g0233 others(3): Show |
6 | HG01069.hp1 HG01361.hp2 HG01978.hp1 others(3): Show |
intron_variant | MODIFIER | c.161-22085G>A | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43728826 | |||||||
| chr11:43729252 | T | C | 18 | a0001c0001t0001g0111 a0001c0001t0001g0112 a0001c0001t0003g0013 others(15): Show |
18 | HG00280.hp1 HG00609.hp2 HG02055.hp1 others(15): Show |
intron_variant | MODIFIER | c.161-21659T>C | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43729252 | |||||||
| chr11:43729434 | A | G | 1 | a0001c0001t0001g0186 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.161-21477A>G | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43729434 | |||||||
| chr11:43729536 | T | C | 18 | a0001c0001t0001g0111 a0001c0001t0001g0112 a0001c0001t0003g0013 others(15): Show |
18 | HG00280.hp1 HG00609.hp2 HG02055.hp1 others(15): Show |
intron_variant | MODIFIER | c.161-21375T>C | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43729536 | |||||||
| chr11:43729600 | G | A | 2 | a0001c0003t0001g0225 a0001c0003t0001g0272 |
2 | HG00140.hp1 HG01167.hp2 |
intron_variant | MODIFIER | c.161-21311G>A | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43729600 | |||||||
| chr11:43729649 | T | C | 3 | a0001c0001t0001g0111 a0001c0001t0001g0112 a0001c0001t0003g0206 |
3 | HG02055.hp1 HG02809.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.161-21262T>C | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43729649 | |||||||
| chr11:43729762 | A | G | 1 | a0002c0002t0002g0151 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.161-21149A>G | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43729762 | |||||||
| chr11:43730014 | A | AT | 23 | a0001c0001t0001g0009 a0001c0001t0001g0186 a0001c0001t0001g0208 others(20): Show |
23 | HG00099.hp2 HG00140.hp1 HG01167.hp2 others(20): Show |
intron_variant | MODIFIER | c.161-20896dupT | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr11 | 43730014 | ||||||
| chr11:43730022 | T | C | 1 | a0002c0002t0002g0140 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.161-20889T>C | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43730022 | |||||||
| chr11:43730040 | G | C | 6 | a0002c0002t0002g0166 a0002c0002t0002g0167 a0002c0002t0002g0168 others(3): Show |
6 | HG00280.hp2 HG00738.hp1 HG01099.hp1 others(3): Show |
intron_variant | MODIFIER | c.161-20871G>C | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43730040 | |||||||
| chr11:43730048 | T | G | 13 | a0001c0001t0001g0128 a0001c0001t0001g0129 a0001c0003t0001g0197 others(10): Show |
13 | HG00639.hp2 HG00642.hp2 HG01069.hp1 others(10): Show |
intron_variant | MODIFIER | c.161-20863T>G | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43730048 | |||||||
| chr11:43730304 | G | T | 3 | a0002c0002t0004g0205 a0002c0002t0004g0274 a0002c0002t0009g0200 |
3 | HG02451.hp1 HG02970.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.161-20607G>T | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43730304 | |||||||
| chr11:43730359 | G | A | 1 | a0002c0002t0002g0039 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.161-20552G>A | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43730359 | |||||||
| chr11:43730746 | C | T | 3 | a0002c0002t0002g0187 a0002c0002t0002g0188 a0002c0002t0002g0189 |
3 | HG00140.hp2 HG01167.hp1 HG01346.hp1 |
intron_variant | MODIFIER | c.161-20165C>T | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43730746 | |||||||
| chr11:43730965 | A | G | 1 | a0002c0002t0002g0175 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.161-19946A>G | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43730965 | |||||||
| chr11:43730972 | G | A | 182 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(179): Show |
183 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(180): Show |
intron_variant | MODIFIER | c.161-19939G>A | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43730972 | |||||||
| chr11:43730983 | A | G | 19 | a0001c0001t0001g0111 a0001c0001t0001g0112 a0001c0001t0003g0013 others(16): Show |
19 | HG00280.hp1 HG00609.hp2 HG02055.hp1 others(16): Show |
intron_variant | MODIFIER | c.161-19928A>G | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43730983 | |||||||
| chr11:43730998 | T | C | 18 | a0001c0001t0001g0111 a0001c0001t0001g0112 a0001c0001t0003g0013 others(15): Show |
18 | HG00280.hp1 HG00609.hp2 HG02055.hp1 others(15): Show |
intron_variant | MODIFIER | c.161-19913T>C | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43730998 | |||||||
| chr11:43731089 | C | T | 3 | a0001c0001t0001g0060 a0001c0001t0001g0061 a0001c0001t0001g0062 |
3 | HG03453.hp2 HG03471.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.161-19822C>T | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43731089 | |||||||
| chr11:43731098 | G | C | 4 | a0001c0001t0003g0267 a0001c0001t0003g0268 a0001c0001t0003g0278 others(1): Show |
4 | HG02572.hp1 HG02965.hp2 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.161-19813G>C | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43731098 | |||||||
| chr11:43731439 | C | T | 14 | a0001c0001t0003g0013 a0001c0001t0003g0014 a0001c0001t0003g0015 others(11): Show |
14 | HG00280.hp1 HG00609.hp2 NA18612.hp2 others(11): Show |
intron_variant | MODIFIER | c.161-19472C>T | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43731439 | |||||||
| chr11:43731564 | T | A | 19 | a0001c0001t0001g0128 a0001c0001t0001g0129 a0001c0001t0001g0265 others(16): Show |
19 | HG00639.hp2 HG00642.hp2 HG01069.hp1 others(16): Show |
intron_variant | MODIFIER | c.161-19347T>A | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43731564 | |||||||
| chr11:43731643 | G | T | 1 | a0001c0001t0001g0078 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.161-19268G>T | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43731643 | |||||||
| chr11:43731914 | C | T | 18 | a0001c0001t0001g0111 a0001c0001t0001g0112 a0001c0001t0003g0013 others(15): Show |
18 | HG00280.hp1 HG00609.hp2 HG02055.hp1 others(15): Show |
intron_variant | MODIFIER | c.161-18997C>T | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43731914 | |||||||
| chr11:43731963 | G | A | 1 | a0001c0003t0001g0238 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.161-18948G>A | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43731963 | |||||||
| chr11:43732111 | G | C | 19 | a0001c0001t0001g0128 a0001c0001t0001g0129 a0001c0001t0001g0265 others(16): Show |
19 | HG00639.hp2 HG00642.hp2 HG01069.hp1 others(16): Show |
intron_variant | MODIFIER | c.161-18800G>C | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43732111 | |||||||
| chr11:43732175 | G | C | 182 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(179): Show |
183 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(180): Show |
intron_variant | MODIFIER | c.161-18736G>C | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43732175 | |||||||
| chr11:43732272 | G | A | 1 | a0001c0001t0001g0152 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.161-18639G>A | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43732272 | |||||||
| chr11:43732610 | G | A | 10 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(7): Show |
10 | HG01884.hp2 HG02257.hp1 HG02717.hp2 others(7): Show |
intron_variant | MODIFIER | c.161-18301G>A | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43732610 | |||||||
| chr11:43732822 | A | G | 182 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(179): Show |
183 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(180): Show |
intron_variant | MODIFIER | c.161-18089A>G | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43732822 | |||||||
| chr11:43732830 | T | C | 1 | a0001c0001t0001g0257 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.161-18081T>C | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43732830 | |||||||
| chr11:43733059 | C | A | 13 | a0001c0001t0003g0267 a0001c0001t0003g0268 a0001c0001t0003g0278 others(10): Show |
13 | HG01070.hp2 HG01071.hp1 HG02004.hp1 others(10): Show |
intron_variant | MODIFIER | c.161-17852C>A | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43733059 | |||||||
| chr11:43733498 | A | G | 1 | a0001c0001t0003g0023 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.161-17413A>G | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43733498 | |||||||
| chr11:43733527 | C | T | 2 | a0001c0003t0003g0231 a0001c0003t0003g0232 |
2 | HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.161-17384C>T | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43733527 | |||||||
| chr11:43733551 | G | A | 1 | a0001c0001t0001g0054 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.161-17360G>A | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43733551 | |||||||
| chr11:43733594 | A | G | 1 | a0001c0007t0001g0230 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.161-17317A>G | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43733594 | |||||||
| chr11:43733682 | T | A | 13 | a0001c0001t0003g0267 a0001c0001t0003g0268 a0001c0001t0003g0278 others(10): Show |
13 | HG01070.hp2 HG01071.hp1 HG02004.hp1 others(10): Show |
intron_variant | MODIFIER | c.161-17229T>A | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43733682 | |||||||
| chr11:43733796 | G | A | 1 | a0001c0001t0001g0047 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.161-17115G>A | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43733796 | |||||||
| chr11:43733868 | C | A | 1 | a0001c0001t0001g0255 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.161-17043C>A | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43733868 | |||||||
| chr11:43733888 | G | A | 5 | a0002c0002t0002g0161 a0002c0002t0002g0175 a0002c0002t0002g0176 others(2): Show |
5 | HG02647.hp1 HG02723.hp1 HG03130.hp2 others(2): Show |
intron_variant | MODIFIER | c.161-17023G>A | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43733888 | |||||||
| chr11:43734107 | T | G | 1 | a0002c0002t0002g0144 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.161-16804T>G | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43734107 | |||||||
| chr11:43734174 | C | T | 14 | a0001c0001t0003g0013 a0001c0001t0003g0014 a0001c0001t0003g0015 others(11): Show |
14 | HG00280.hp1 HG00609.hp2 NA18612.hp2 others(11): Show |
intron_variant | MODIFIER | c.161-16737C>T | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43734174 | |||||||
| chr11:43734230 | C | T | 55 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(52): Show |
55 | HG00099.hp2 HG00140.hp1 HG00639.hp2 others(52): Show |
intron_variant | MODIFIER | c.161-16681C>T | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43734230 | |||||||
| chr11:43734293 | A | C | 14 | a0001c0001t0003g0013 a0001c0001t0003g0014 a0001c0001t0003g0015 others(11): Show |
14 | HG00280.hp1 HG00609.hp2 NA18612.hp2 others(11): Show |
intron_variant | MODIFIER | c.161-16618A>C | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43734293 | |||||||
| chr11:43734294 | G | T | 1 | a0002c0002t0006g0108 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.161-16617G>T | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43734294 | |||||||
| chr11:43734380 | C | T | 1 | a0001c0001t0001g0028 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.161-16531C>T | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43734380 | |||||||
| chr11:43734411 | G | C | 1 | a0002c0002t0009g0200 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.161-16500G>C | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43734411 | |||||||
| chr11:43734578 | T | A | 2 | a0002c0002t0002g0126 a0002c0002t0002g0182 |
2 | NA18964.hp1 NA19000.hp1 |
intron_variant | MODIFIER | c.161-16333T>A | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43734578 | |||||||
| chr11:43734601 | T | TG | 182 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(179): Show |
183 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(180): Show |
intron_variant | MODIFIER | c.161-16308dupG | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr11 | 43734601 | ||||||
| chr11:43734777 | C | G | 1 | a0002c0002t0009g0200 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.161-16134C>G | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43734777 | |||||||
| chr11:43734839 | C | G | 1 | a0001c0007t0001g0230 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.161-16072C>G | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43734839 | |||||||
| chr11:43734886 | A | T | 5 | a0002c0002t0002g0161 a0002c0002t0002g0175 a0002c0002t0002g0176 others(2): Show |
5 | HG02647.hp1 HG02723.hp1 HG03130.hp2 others(2): Show |
intron_variant | MODIFIER | c.161-16025A>T | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43734886 | |||||||
| chr11:43734910 | C | T | 15 | a0001c0001t0003g0013 a0001c0001t0003g0014 a0001c0001t0003g0015 others(12): Show |
15 | HG00280.hp1 HG00609.hp2 HG02258.hp1 others(12): Show |
intron_variant | MODIFIER | c.161-16001C>T | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43734910 | |||||||
| chr11:43734928 | T | C | 2 | a0001c0001t0001g0006 a0001c0001t0001g0010 |
2 | HG02257.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.161-15983T>C | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43734928 | |||||||
| chr11:43735321 | G | A | 1 | a0001c0001t0003g0023 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.161-15590G>A | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43735321 | |||||||
| chr11:43735334 | A | G | 2 | a0001c0001t0001g0006 a0001c0001t0001g0010 |
2 | HG02257.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.161-15577A>G | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43735334 | |||||||
| chr11:43735471 | A | G | 1 | a0001c0001t0001g0054 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.161-15440A>G | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43735471 | |||||||
| chr11:43735967 | T | C | 15 | a0001c0001t0003g0013 a0001c0001t0003g0014 a0001c0001t0003g0015 others(12): Show |
15 | HG00280.hp1 HG00609.hp2 HG02258.hp1 others(12): Show |
intron_variant | MODIFIER | c.161-14944T>C | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43735967 | |||||||
| chr11:43736220 | G | A | 1 | a0001c0001t0001g0186 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.161-14691G>A | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43736220 | |||||||
| chr11:43736432 | C | T | 3 | a0001c0001t0001g0006 a0001c0001t0001g0010 a0001c0001t0001g0043 |
3 | HG02257.hp1 NA18522.hp1 NA19080.hp1 |
intron_variant | MODIFIER | c.161-14479C>T | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43736432 | |||||||
| chr11:43737102 | C | T | 14 | a0001c0001t0003g0013 a0001c0001t0003g0014 a0001c0001t0003g0015 others(11): Show |
14 | HG00280.hp1 HG00609.hp2 NA18612.hp2 others(11): Show |
intron_variant | MODIFIER | c.161-13809C>T | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43737102 | |||||||
| chr11:43737388 | G | A | 2 | a0001c0001t0001g0069 a0001c0001t0001g0105 |
2 | HG01928.hp1 NA19000.hp2 |
intron_variant | MODIFIER | c.161-13523G>A | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43737388 | |||||||
| chr11:43737397 | C | T | 2 | a0002c0002t0002g0168 a0002c0002t0002g0169 |
2 | HG01346.hp2 HG01358.hp2 |
intron_variant | MODIFIER | c.161-13514C>T | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43737397 | |||||||
| chr11:43737621 | T | A | 1 | a0001c0001t0001g0026 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.161-13290T>A | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43737621 | |||||||
| chr11:43737772 | A | G | 1 | a0001c0001t0003g0206 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.161-13139A>G | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43737772 | |||||||
| chr11:43737840 | G | A | 1 | a0001c0003t0001g0198 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.161-13071G>A | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43737840 | |||||||
| chr11:43737940 | G | A | 8 | a0002c0002t0002g0127 a0002c0002t0002g0140 a0002c0002t0002g0147 others(5): Show |
8 | HG00140.hp2 HG01070.hp1 HG01167.hp1 others(5): Show |
intron_variant | MODIFIER | c.161-12971G>A | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43737940 | |||||||
| chr11:43737945 | C | T | 10 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(7): Show |
10 | HG01884.hp2 HG02257.hp1 HG02717.hp2 others(7): Show |
intron_variant | MODIFIER | c.161-12966C>T | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43737945 | |||||||
| chr11:43737966 | G | A | 23 | a0001c0001t0001g0009 a0001c0001t0001g0186 a0001c0001t0001g0208 others(20): Show |
23 | HG00099.hp2 HG00140.hp1 HG01167.hp2 others(20): Show |
intron_variant | MODIFIER | c.161-12945G>A | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43737966 | |||||||
| chr11:43737998 | G | T | 1 | a0001c0001t0001g0255 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.161-12913G>T | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43737998 | |||||||
| chr11:43738000 | C | G | 1 | a0001c0001t0001g0255 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.161-12911C>G | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43738000 | |||||||
| chr11:43738001 | A | G | 1 | a0001c0001t0001g0255 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.161-12910A>G | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43738001 | |||||||
| chr11:43738056 | C | CA | 41 | a0001c0001t0001g0009 a0001c0001t0001g0047 a0001c0001t0001g0053 others(38): Show |
41 | HG00099.hp2 HG00140.hp1 HG01070.hp2 others(38): Show |
intron_variant | MODIFIER | c.161-12835dupA | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr11 | 43738056 | ||||||
| chr11:43738056 | CA | C | 58 | a0001c0001t0001g0005 a0001c0001t0001g0007 a0001c0001t0001g0008 others(55): Show |
58 | HG00280.hp2 HG00423.hp1 HG00642.hp2 others(55): Show |
intron_variant | MODIFIER | c.161-12835delA | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr11 | 43738056 | ||||||
| chr11:43738056 | CAA | C | 15 | a0001c0001t0003g0013 a0001c0001t0003g0014 a0001c0001t0003g0015 others(12): Show |
15 | HG00280.hp1 HG00609.hp2 HG02258.hp1 others(12): Show |
intron_variant | MODIFIER | c.161-12836_161-1283 others(6): Show |
HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr11 | 43738056 | ||||||
| chr11:43738075 | AAT | A | 11 | a0001c0001t0001g0002 a0001c0001t0001g0120 a0001c0001t0001g0121 others(8): Show |
12 | HG01496.hp1 HG02258.hp2 HG02280.hp1 others(9): Show |
intron_variant | MODIFIER | c.161-12834_161-1283 others(6): Show |
HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr11 | 43738075 | ||||||
| chr11:43738076 | AT | A | 5 | a0001c0001t0001g0123 a0001c0001t0001g0256 a0001c0001t0001g0257 others(2): Show |
5 | HG01109.hp1 HG02896.hp2 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.161-12834delT | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43738076 | |||||||
| chr11:43738118 | AAGCATGT others(18): Show |
A | 53 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(50): Show |
53 | HG00099.hp2 HG00140.hp1 HG00639.hp2 others(50): Show |
intron_variant | MODIFIER | c.161-12783_161-1275 others(29): Show |
HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr11 | 43738118 | ||||||
| chr11:43738338 | T | G | 1 | a0001c0001t0003g0020 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.161-12573T>G | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43738338 | |||||||
| chr11:43738385 | C | T | 3 | a0001c0001t0001g0005 a0001c0001t0001g0007 a0001c0001t0001g0008 |
3 | HG02809.hp1 HG02886.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.161-12526C>T | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43738385 | |||||||
| chr11:43738665 | C | T | 3 | a0001c0001t0001g0044 a0001c0001t0001g0051 a0001c0001t0001g0052 |
3 | HG01516.hp2 HG02004.hp2 HG02055.hp2 |
intron_variant | MODIFIER | c.161-12246C>T | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43738665 | |||||||
| chr11:43739009 | T | G | 2 | a0002c0002t0008g0003 a0002c0002t0009g0200 |
2 | NA18906.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.161-11902T>G | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43739009 | |||||||
| chr11:43739057 | A | G | 97 | a0001c0001t0001g0002 a0001c0001t0001g0026 a0001c0001t0001g0028 others(94): Show |
98 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(95): Show |
intron_variant | MODIFIER | c.161-11854A>G | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43739057 | |||||||
| chr11:43739070 | G | T | 1 | a0001c0001t0001g0081 | 1 | HG02273.hp2 | intron_variant | MODIFIER | c.161-11841G>T | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43739070 | |||||||
| chr11:43739084 | C | G | 3 | a0002c0002t0002g0148 a0002c0002t0002g0149 a0002c0002t0006g0108 |
3 | HG00735.hp1 NA18941.hp1 NA19064.hp2 |
intron_variant | MODIFIER | c.161-11827C>G | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43739084 | |||||||
| chr11:43739185 | G | T | 97 | a0001c0001t0001g0002 a0001c0001t0001g0026 a0001c0001t0001g0028 others(94): Show |
98 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(95): Show |
intron_variant | MODIFIER | c.161-11726G>T | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43739185 | |||||||
| chr11:43739240 | G | A | 14 | a0001c0001t0003g0013 a0001c0001t0003g0014 a0001c0001t0003g0015 others(11): Show |
14 | HG00280.hp1 HG00609.hp2 NA18612.hp2 others(11): Show |
intron_variant | MODIFIER | c.161-11671G>A | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43739240 | |||||||
| chr11:43739563 | C | G | 1 | a0002c0002t0002g0177 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.161-11348C>G | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43739563 | |||||||
| chr11:43739701 | T | TC | 220 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(217): Show |
221 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(218): Show |
intron_variant | MODIFIER | c.161-11210_161-1120 others(5): Show |
HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43739701 | |||||||
| chr11:43740075 | C | T | 5 | a0002c0002t0002g0161 a0002c0002t0002g0175 a0002c0002t0002g0176 others(2): Show |
5 | HG02647.hp1 HG02723.hp1 HG03130.hp2 others(2): Show |
intron_variant | MODIFIER | c.161-10836C>T | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43740075 | |||||||
| chr11:43740164 | A | T | 15 | a0001c0001t0003g0013 a0001c0001t0003g0014 a0001c0001t0003g0015 others(12): Show |
15 | HG00280.hp1 HG00609.hp2 HG02258.hp1 others(12): Show |
intron_variant | MODIFIER | c.161-10747A>T | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43740164 | |||||||
| chr11:43740239 | G | T | 1 | a0002c0002t0006g0108 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.161-10672G>T | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43740239 | |||||||
| chr11:43740242 | C | T | 15 | a0001c0001t0003g0013 a0001c0001t0003g0014 a0001c0001t0003g0015 others(12): Show |
15 | HG00280.hp1 HG00609.hp2 HG02258.hp1 others(12): Show |
intron_variant | MODIFIER | c.161-10669C>T | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43740242 | |||||||
| chr11:43740267 | C | T | 15 | a0001c0001t0003g0013 a0001c0001t0003g0014 a0001c0001t0003g0015 others(12): Show |
15 | HG00280.hp1 HG00609.hp2 HG02258.hp1 others(12): Show |
intron_variant | MODIFIER | c.161-10644C>T | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43740267 | |||||||
| chr11:43740459 | A | G | 21 | a0001c0001t0001g0002 a0001c0001t0001g0111 a0001c0001t0001g0112 others(18): Show |
22 | HG01109.hp1 HG01496.hp1 HG02055.hp1 others(19): Show |
intron_variant | MODIFIER | c.161-10452A>G | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43740459 | |||||||
| chr11:43740660 | A | G | 53 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(50): Show |
53 | HG00099.hp2 HG00140.hp1 HG00639.hp2 others(50): Show |
intron_variant | MODIFIER | c.161-10251A>G | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43740660 | |||||||
| chr11:43740945 | C | T | 1 | a0001c0001t0001g0042 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.161-9966C>T | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43740945 | |||||||
| chr11:43741000 | G | A | 1 | a0001c0001t0003g0013 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.161-9911G>A | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43741000 | |||||||
| chr11:43741154 | A | G | 14 | a0001c0001t0003g0013 a0001c0001t0003g0014 a0001c0001t0003g0015 others(11): Show |
14 | HG00280.hp1 HG00609.hp2 NA18612.hp2 others(11): Show |
intron_variant | MODIFIER | c.161-9757A>G | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43741154 | |||||||
| chr11:43741336 | C | T | 5 | a0001c0001t0001g0111 a0001c0001t0001g0112 a0001c0001t0001g0202 others(2): Show |
5 | HG02055.hp1 HG02559.hp2 HG02809.hp2 others(2): Show |
intron_variant | MODIFIER | c.161-9575C>T | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43741336 | |||||||
| chr11:43741455 | T | TA | 14 | a0001c0001t0003g0013 a0001c0001t0003g0014 a0001c0001t0003g0015 others(11): Show |
14 | HG00280.hp1 HG00609.hp2 NA18612.hp2 others(11): Show |
intron_variant | MODIFIER | c.161-9447dupA | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr11 | 43741455 | ||||||
| chr11:43741803 | G | A | 1 | a0001c0001t0001g0113 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.161-9108G>A | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43741803 | |||||||
| chr11:43741819 | C | T | 15 | a0001c0001t0003g0013 a0001c0001t0003g0014 a0001c0001t0003g0015 others(12): Show |
15 | HG00280.hp1 HG00609.hp2 HG02258.hp1 others(12): Show |
intron_variant | MODIFIER | c.161-9092C>T | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43741819 | |||||||
| chr11:43741820 | C | T | 15 | a0001c0001t0003g0013 a0001c0001t0003g0014 a0001c0001t0003g0015 others(12): Show |
15 | HG00280.hp1 HG00609.hp2 HG02258.hp1 others(12): Show |
intron_variant | MODIFIER | c.161-9091C>T | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43741820 | |||||||
| chr11:43741915 | T | C | 3 | a0001c0001t0001g0060 a0001c0001t0001g0061 a0001c0001t0001g0062 |
3 | HG03453.hp2 HG03471.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.161-8996T>C | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43741915 | |||||||
| chr11:43742019 | C | G | 1 | a0001c0001t0001g0010 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.161-8892C>G | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43742019 | |||||||
| chr11:43742112 | A | AAT | 5 | a0001c0001t0001g0036 a0001c0001t0001g0047 a0001c0001t0001g0055 others(2): Show |
5 | HG00099.hp1 HG00323.hp2 HG01361.hp1 others(2): Show |
intron_variant | MODIFIER | c.161-8772_161-8771d others(4): Show |
HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr11 | 43742112 | ||||||
| chr11:43742112 | AAT | A | 8 | a0001c0001t0001g0033 a0001c0001t0001g0111 a0001c0001t0001g0112 others(5): Show |
8 | HG01884.hp2 HG02055.hp1 HG02258.hp1 others(5): Show |
intron_variant | MODIFIER | c.161-8772_161-8771d others(4): Show |
HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr11 | 43742112 | ||||||
| chr11:43742112 | AATAT | A | 44 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(41): Show |
44 | HG00099.hp2 HG00140.hp1 HG00639.hp2 others(41): Show |
intron_variant | MODIFIER | c.161-8774_161-8771d others(6): Show |
HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr11 | 43742112 | ||||||
| chr11:43742112 | AATATAT | A | 3 | a0002c0002t0002g0192 a0002c0002t0002g0193 a0002c0002t0002g0194 |
3 | HG02559.hp1 HG03516.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.161-8776_161-8771d others(8): Show |
HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr11 | 43742112 | ||||||
| chr11:43742132 | TATA | T | 20 | a0001c0001t0001g0002 a0001c0001t0001g0120 a0001c0001t0001g0121 others(17): Show |
21 | HG01109.hp1 HG01361.hp2 HG01496.hp1 others(18): Show |
intron_variant | MODIFIER | c.161-8778_161-8776d others(5): Show |
HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43742132 | |||||||
| chr11:43742134 | TATA | T | 15 | a0001c0001t0001g0271 a0001c0001t0003g0014 a0001c0001t0003g0015 others(12): Show |
15 | HG00280.hp1 HG00609.hp2 HG06807.hp1 others(12): Show |
intron_variant | MODIFIER | c.161-8776_161-8774d others(5): Show |
HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43742134 | |||||||
| chr11:43742135 | A | T | 4 | a0001c0001t0001g0186 a0001c0001t0001g0257 a0002c0002t0002g0126 others(1): Show |
4 | HG01891.hp2 HG02922.hp2 NA18964.hp1 others(1): Show |
intron_variant | MODIFIER | c.161-8776A>T | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43742135 | |||||||
| chr11:43742137 | A | ATT | 12 | a0001c0001t0001g0034 a0001c0001t0001g0046 a0001c0001t0001g0051 others(9): Show |
12 | HG01346.hp2 HG01358.hp2 HG02004.hp2 others(9): Show |
intron_variant | MODIFIER | c.161-8773_161-8772i others(4): Show |
HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr11 | 43742137 | ||||||
| chr11:43742137 | A | T | 86 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(83): Show |
87 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(84): Show |
intron_variant | MODIFIER | c.161-8774A>T | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43742137 | |||||||
| chr11:43742139 | A | AT | 5 | a0002c0002t0002g0151 a0002c0002t0002g0161 a0002c0002t0002g0176 others(2): Show |
5 | HG02723.hp1 HG03130.hp2 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.161-8761dupT | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr11 | 43742139 | ||||||
| chr11:43742139 | A | ATATATAT others(3): Show |
3 | a0001c0003t0003g0244 a0001c0003t0003g0245 a0002c0002t0002g0160 |
3 | HG02004.hp1 HG02155.hp2 HG03239.hp2 |
intron_variant | MODIFIER | c.161-8771_161-8770i others(12): Show |
HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr11 | 43742139 | ||||||
| chr11:43742139 | A | ATATATAT others(5): Show |
1 | a0002c0002t0004g0205 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.161-8771_161-8770i others(14): Show |
HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr11 | 43742139 | ||||||
| chr11:43742139 | A | ATATATTT others(1): Show |
6 | a0001c0003t0003g0242 a0001c0003t0003g0243 a0001c0003t0003g0246 others(3): Show |
6 | HG01070.hp2 HG01071.hp1 HG02970.hp1 others(3): Show |
intron_variant | MODIFIER | c.161-8771_161-8770i others(10): Show |
HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr11 | 43742139 | ||||||
| chr11:43742139 | A | ATATT | 8 | a0001c0001t0001g0026 a0001c0001t0001g0028 a0001c0001t0001g0056 others(5): Show |
8 | HG00738.hp2 HG01123.hp2 HG02155.hp1 others(5): Show |
intron_variant | MODIFIER | c.161-8771_161-8770i others(6): Show |
HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr11 | 43742139 | ||||||
| chr11:43742139 | A | ATT | 59 | a0001c0001t0001g0029 a0001c0001t0001g0030 a0001c0001t0001g0031 others(56): Show |
59 | HG00408.hp1 HG00423.hp2 HG00735.hp2 others(56): Show |
intron_variant | MODIFIER | c.161-8762_161-8761d others(4): Show |
HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr11 | 43742139 | ||||||
| chr11:43742139 | A | T | 166 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(163): Show |
168 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(165): Show |
intron_variant | MODIFIER | c.161-8772A>T | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43742139 | |||||||
| chr11:43742140 | T | TATATATA others(2): Show |
4 | a0001c0001t0003g0267 a0001c0001t0003g0268 a0001c0001t0003g0278 others(1): Show |
4 | HG02572.hp1 HG02965.hp2 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.161-8771_161-8770i others(11): Show |
HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43742140 | |||||||
| chr11:43742141 | T | A | 1 | a0002c0002t0009g0200 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.161-8770T>A | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43742141 | |||||||
| chr11:43742142 | T | A | 4 | a0001c0001t0003g0267 a0001c0001t0003g0268 a0001c0001t0003g0278 others(1): Show |
4 | HG02572.hp1 HG02965.hp2 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.161-8769T>A | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43742142 | |||||||
| chr11:43742151 | A | T | 1 | a0001c0001t0001g0196 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.161-8760A>T | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43742151 | |||||||
| chr11:43742531 | T | C | 3 | a0001c0001t0001g0029 a0001c0001t0001g0035 a0001c0001t0001g0048 |
3 | HG02135.hp2 NA19070.hp2 NA19090.hp2 |
intron_variant | MODIFIER | c.161-8380T>C | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43742531 | |||||||
| chr11:43742752 | G | T | 19 | a0001c0001t0001g0111 a0001c0001t0001g0112 a0001c0001t0001g0202 others(16): Show |
19 | HG00280.hp1 HG00609.hp2 HG02055.hp1 others(16): Show |
intron_variant | MODIFIER | c.161-8159G>T | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43742752 | |||||||
| chr11:43742754 | G | T | 15 | a0001c0001t0003g0013 a0001c0001t0003g0014 a0001c0001t0003g0015 others(12): Show |
15 | HG00280.hp1 HG00609.hp2 HG02258.hp1 others(12): Show |
intron_variant | MODIFIER | c.161-8157G>T | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43742754 | |||||||
| chr11:43742756 | G | T | 15 | a0001c0001t0003g0013 a0001c0001t0003g0014 a0001c0001t0003g0015 others(12): Show |
15 | HG00280.hp1 HG00609.hp2 HG02258.hp1 others(12): Show |
intron_variant | MODIFIER | c.161-8155G>T | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43742756 | |||||||
| chr11:43742758 | G | GT | 14 | a0001c0001t0003g0013 a0001c0001t0003g0014 a0001c0001t0003g0015 others(11): Show |
14 | HG00280.hp1 HG00609.hp2 NA18612.hp2 others(11): Show |
intron_variant | MODIFIER | c.161-8152dupT | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr11 | 43742758 | ||||||
| chr11:43742760 | G | GT | 9 | a0001c0001t0001g0005 a0001c0001t0001g0007 a0001c0001t0001g0008 others(6): Show |
9 | HG01175.hp2 HG01884.hp2 HG02809.hp1 others(6): Show |
intron_variant | MODIFIER | c.161-8141dupT | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr11 | 43742760 | ||||||
| chr11:43742760 | G | T | 16 | a0001c0001t0001g0078 a0001c0001t0003g0013 a0001c0001t0003g0014 others(13): Show |
16 | HG00280.hp1 HG00609.hp2 HG02258.hp1 others(13): Show |
intron_variant | MODIFIER | c.161-8151G>T | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43742760 | |||||||
| chr11:43742762 | T | G | 1 | a0001c0001t0001g0097 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.161-8149T>G | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43742762 | |||||||
| chr11:43742790 | A | G | 15 | a0001c0001t0003g0013 a0001c0001t0003g0014 a0001c0001t0003g0015 others(12): Show |
15 | HG00280.hp1 HG00609.hp2 HG02258.hp1 others(12): Show |
intron_variant | MODIFIER | c.161-8121A>G | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43742790 | |||||||
| chr11:43743033 | A | G | 4 | a0002c0002t0002g0001 a0002c0002t0002g0025 a0002c0002t0002g0038 others(1): Show |
5 | HG00642.hp1 HG01069.hp2 HG01071.hp2 others(2): Show |
intron_variant | MODIFIER | c.161-7878A>G | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43743033 | |||||||
| chr11:43743260 | T | G | 14 | a0001c0001t0003g0013 a0001c0001t0003g0014 a0001c0001t0003g0015 others(11): Show |
14 | HG00280.hp1 HG00609.hp2 NA18612.hp2 others(11): Show |
intron_variant | MODIFIER | c.161-7651T>G | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43743260 | |||||||
| chr11:43743372 | T | C | 1 | a0005c0006t0012g0021 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.161-7539T>C | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43743372 | |||||||
| chr11:43743436 | A | C | 1 | a0001c0001t0001g0046 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.161-7475A>C | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43743436 | |||||||
| chr11:43744139 | T | G | 1 | a0002c0002t0008g0003 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.161-6772T>G | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43744139 | |||||||
| chr11:43744356 | T | TA | 25 | a0001c0001t0001g0002 a0001c0001t0001g0120 a0001c0001t0001g0121 others(22): Show |
26 | HG00280.hp1 HG00609.hp2 HG01109.hp1 others(23): Show |
intron_variant | MODIFIER | c.161-6545dupA | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr11 | 43744356 | ||||||
| chr11:43744400 | G | A | 23 | a0001c0001t0001g0009 a0001c0001t0001g0186 a0001c0001t0001g0208 others(20): Show |
23 | HG00099.hp2 HG00140.hp1 HG01167.hp2 others(20): Show |
intron_variant | MODIFIER | c.161-6511G>A | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43744400 | |||||||
| chr11:43744640 | C | G | 1 | a0001c0001t0001g0055 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.161-6271C>G | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43744640 | |||||||
| chr11:43744764 | A | T | 1 | a0001c0001t0003g0206 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.161-6147A>T | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43744764 | |||||||
| chr11:43744784 | G | T | 13 | a0001c0001t0003g0013 a0001c0001t0003g0014 a0001c0001t0003g0015 others(10): Show |
13 | HG00609.hp2 NA18612.hp2 NA18747.hp1 others(10): Show |
intron_variant | MODIFIER | c.161-6127G>T | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43744784 | |||||||
| chr11:43745274 | G | A | 15 | a0001c0001t0003g0013 a0001c0001t0003g0014 a0001c0001t0003g0015 others(12): Show |
15 | HG00280.hp1 HG00609.hp2 HG02258.hp1 others(12): Show |
intron_variant | MODIFIER | c.161-5637G>A | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43745274 | |||||||
| chr11:43745352 | T | C | 182 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(179): Show |
183 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(180): Show |
intron_variant | MODIFIER | c.161-5559T>C | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43745352 | |||||||
| chr11:43745480 | A | G | 1 | a0001c0003t0001g0229 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.161-5431A>G | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43745480 | |||||||
| chr11:43745964 | C | T | 14 | a0001c0001t0003g0013 a0001c0001t0003g0014 a0001c0001t0003g0015 others(11): Show |
14 | HG00280.hp1 HG00609.hp2 NA18612.hp2 others(11): Show |
intron_variant | MODIFIER | c.161-4947C>T | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43745964 | |||||||
| chr11:43746000 | A | T | 2 | a0001c0001t0001g0128 a0001c0001t0001g0129 |
2 | HG02738.hp1 NA20905.hp1 |
intron_variant | MODIFIER | c.161-4911A>T | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43746000 | |||||||
| chr11:43746034 | A | G | 2 | a0001c0003t0003g0231 a0001c0003t0003g0232 |
2 | HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.161-4877A>G | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43746034 | |||||||
| chr11:43746246 | T | C | 111 | a0001c0001t0001g0002 a0001c0001t0001g0026 a0001c0001t0001g0028 others(108): Show |
112 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(109): Show |
intron_variant | MODIFIER | c.161-4665T>C | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43746246 | |||||||
| chr11:43746301 | A | G | 16 | a0001c0001t0001g0002 a0001c0001t0001g0120 a0001c0001t0001g0121 others(13): Show |
17 | HG01109.hp1 HG01496.hp1 HG02258.hp2 others(14): Show |
intron_variant | MODIFIER | c.161-4610A>G | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43746301 | |||||||
| chr11:43746649 | G | A | 1 | a0001c0001t0001g0054 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.161-4262G>A | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43746649 | |||||||
| chr11:43746704 | A | G | 182 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(179): Show |
183 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(180): Show |
intron_variant | MODIFIER | c.161-4207A>G | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43746704 | |||||||
| chr11:43746928 | T | G | 11 | a0002c0002t0002g0004 a0002c0002t0002g0138 a0002c0002t0002g0142 others(8): Show |
11 | HG01109.hp2 HG01884.hp1 HG02257.hp2 others(8): Show |
intron_variant | MODIFIER | c.161-3983T>G | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43746928 | |||||||
| chr11:43746933 | A | G | 14 | a0001c0001t0003g0013 a0001c0001t0003g0014 a0001c0001t0003g0015 others(11): Show |
14 | HG00280.hp1 HG00609.hp2 NA18612.hp2 others(11): Show |
intron_variant | MODIFIER | c.161-3978A>G | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43746933 | |||||||
| chr11:43747656 | C | G | 14 | a0001c0001t0003g0013 a0001c0001t0003g0014 a0001c0001t0003g0015 others(11): Show |
14 | HG00280.hp1 HG00609.hp2 NA18612.hp2 others(11): Show |
intron_variant | MODIFIER | c.161-3255C>G | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43747656 | |||||||
| chr11:43747675 | G | A | 2 | a0001c0001t0001g0088 a0001c0001t0001g0091 |
2 | HG00738.hp2 HG02738.hp2 |
intron_variant | MODIFIER | c.161-3236G>A | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43747675 | |||||||
| chr11:43747737 | A | C | 93 | a0001c0001t0001g0026 a0001c0001t0001g0028 a0001c0001t0001g0029 others(90): Show |
93 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(90): Show |
intron_variant | MODIFIER | c.161-3174A>C | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43747737 | |||||||
| chr11:43747745 | C | T | 182 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(179): Show |
183 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(180): Show |
intron_variant | MODIFIER | c.161-3166C>T | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43747745 | |||||||
| chr11:43747880 | GC | G | 10 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(7): Show |
10 | HG01884.hp2 HG02257.hp1 HG02717.hp2 others(7): Show |
intron_variant | MODIFIER | c.161-3026delC | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr11 | 43747880 | ||||||
| chr11:43748041 | C | T | 1 | a0001c0001t0001g0074 | 1 | NA19085.hp2 | intron_variant | MODIFIER | c.161-2870C>T | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43748041 | |||||||
| chr11:43748138 | G | A | 16 | a0001c0001t0001g0002 a0001c0001t0001g0120 a0001c0001t0001g0121 others(13): Show |
17 | HG01109.hp1 HG01496.hp1 HG02258.hp2 others(14): Show |
intron_variant | MODIFIER | c.161-2773G>A | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43748138 | |||||||
| chr11:43748419 | G | A | 1 | a0001c0003t0001g0229 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.161-2492G>A | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43748419 | |||||||
| chr11:43748518 | C | T | 1 | a0001c0001t0001g0065 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.161-2393C>T | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43748518 | |||||||
| chr11:43749375 | C | T | 1 | a0001c0001t0001g0218 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.161-1536C>T | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43749375 | |||||||
| chr11:43749443 | C | T | 2 | a0001c0003t0001g0197 a0001c0003t0001g0198 |
2 | HG03669.hp2 HG04199.hp2 |
intron_variant | MODIFIER | c.161-1468C>T | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43749443 | |||||||
| chr11:43749534 | A | G | 97 | a0001c0001t0001g0002 a0001c0001t0001g0026 a0001c0001t0001g0028 others(94): Show |
98 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(95): Show |
intron_variant | MODIFIER | c.161-1377A>G | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43749534 | |||||||
| chr11:43749552 | A | T | 1 | a0001c0001t0003g0015 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.161-1359A>T | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43749552 | |||||||
| chr11:43749573 | G | A | 2 | a0002c0002t0002g0161 a0002c0002t0002g0176 |
2 | HG03130.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.161-1338G>A | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43749573 | |||||||
| chr11:43749969 | C | A | 1 | a0001c0001t0001g0125 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.161-942C>A | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43749969 | |||||||
| chr11:43750264 | T | A | 1 | a0001c0001t0001g0271 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.161-647T>A | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43750264 | |||||||
| chr11:43750265 | T | A | 1 | a0001c0001t0001g0271 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.161-646T>A | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43750265 | |||||||
| chr11:43750463 | A | G | 1 | a0002c0002t0002g0004 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.161-448A>G | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43750463 | |||||||
| chr11:43750519 | T | C | 16 | a0001c0001t0001g0002 a0001c0001t0001g0120 a0001c0001t0001g0121 others(13): Show |
17 | HG01109.hp1 HG01496.hp1 HG02258.hp2 others(14): Show |
intron_variant | MODIFIER | c.161-392T>C | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43750519 | |||||||
| chr11:43750557 | A | G | 9 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(6): Show |
9 | HG01884.hp2 HG02257.hp1 HG02809.hp1 others(6): Show |
intron_variant | MODIFIER | c.161-354A>G | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43750557 | |||||||
| chr11:43750680 | G | A | 1 | a0001c0001t0001g0063 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.161-231G>A | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43750680 | |||||||
| chr11:43750868 | A | G | 1 | a0001c0001t0001g0259 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.161-43A>G | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 1/10 | chr11 | 43750868 | |||||||
| chr11:43750999 | A | G | 76 | a0001c0001t0001g0026 a0001c0001t0001g0028 a0001c0001t0001g0029 others(73): Show |
76 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(73): Show |
intron_variant | MODIFIER | c.207+42A>G | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 2/10 | chr11 | 43750999 | |||||||
| chr11:43751559 | G | T | 1 | a0001c0001t0001g0043 | 1 | NA19080.hp1 | intron_variant | MODIFIER | c.207+602G>T | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 2/10 | chr11 | 43751559 | |||||||
| chr11:43751759 | T | C | 1 | a0001c0001t0001g0053 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.207+802T>C | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 2/10 | chr11 | 43751759 | |||||||
| chr11:43751834 | T | C | 3 | a0002c0002t0004g0205 a0002c0002t0004g0274 a0002c0002t0009g0200 |
3 | HG02451.hp1 HG02970.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.207+877T>C | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 2/10 | chr11 | 43751834 | |||||||
| chr11:43751857 | T | G | 1 | a0001c0001t0001g0208 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.207+900T>G | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 2/10 | chr11 | 43751857 | |||||||
| chr11:43751955 | C | T | 15 | a0001c0001t0003g0013 a0001c0001t0003g0014 a0001c0001t0003g0015 others(12): Show |
15 | HG00280.hp1 HG00609.hp2 HG02258.hp1 others(12): Show |
intron_variant | MODIFIER | c.207+998C>T | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 2/10 | chr11 | 43751955 | |||||||
| chr11:43752158 | C | T | 3 | a0002c0002t0002g0180 a0004c0005t0002g0011 a0004c0005t0002g0012 |
3 | HG01099.hp2 HG01106.hp2 HG01258.hp1 |
intron_variant | MODIFIER | c.207+1201C>T | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 2/10 | chr11 | 43752158 | |||||||
| chr11:43752263 | T | G | 182 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(179): Show |
183 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(180): Show |
intron_variant | MODIFIER | c.207+1306T>G | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 2/10 | chr11 | 43752263 | |||||||
| chr11:43752283 | C | T | 1 | a0002c0002t0002g0253 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.207+1326C>T | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 2/10 | chr11 | 43752283 | |||||||
| chr11:43752609 | G | A | 1 | a0002c0002t0002g0187 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.208-1437G>A | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 2/10 | chr11 | 43752609 | |||||||
| chr11:43752724 | A | G | 97 | a0001c0001t0001g0002 a0001c0001t0001g0026 a0001c0001t0001g0028 others(94): Show |
98 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(95): Show |
intron_variant | MODIFIER | c.208-1322A>G | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 2/10 | chr11 | 43752724 | |||||||
| chr11:43752881 | C | T | 15 | a0001c0001t0003g0013 a0001c0001t0003g0014 a0001c0001t0003g0015 others(12): Show |
15 | HG00280.hp1 HG00609.hp2 HG02258.hp1 others(12): Show |
intron_variant | MODIFIER | c.208-1165C>T | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 2/10 | chr11 | 43752881 | |||||||
| chr11:43752942 | A | G | 1 | a0002c0002t0002g0144 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.208-1104A>G | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 2/10 | chr11 | 43752942 | |||||||
| chr11:43752992 | A | G | 15 | a0001c0001t0003g0013 a0001c0001t0003g0014 a0001c0001t0003g0015 others(12): Show |
15 | HG00280.hp1 HG00609.hp2 HG02258.hp1 others(12): Show |
intron_variant | MODIFIER | c.208-1054A>G | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 2/10 | chr11 | 43752992 | |||||||
| chr11:43753126 | G | A | 1 | a0001c0007t0001g0230 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.208-920G>A | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 2/10 | chr11 | 43753126 | |||||||
| chr11:43753181 | C | T | 13 | a0001c0001t0003g0267 a0001c0001t0003g0268 a0001c0001t0003g0278 others(10): Show |
13 | HG01070.hp2 HG01071.hp1 HG02004.hp1 others(10): Show |
intron_variant | MODIFIER | c.208-865C>T | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 2/10 | chr11 | 43753181 | |||||||
| chr11:43753318 | T | C | 1 | a0001c0003t0001g0229 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.208-728T>C | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 2/10 | chr11 | 43753318 | |||||||
| chr11:43753384 | CT | C | 273 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(270): Show |
275 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(272): Show |
intron_variant | MODIFIER | c.208-644delT | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr11 | 43753384 | ||||||
| chr11:43753557 | TA | T | 11 | a0001c0001t0001g0009 a0001c0001t0001g0219 a0001c0001t0001g0257 others(8): Show |
11 | HG01261.hp2 HG01496.hp2 HG02572.hp1 others(8): Show |
intron_variant | MODIFIER | c.208-473delA | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr11 | 43753557 | ||||||
| chr11:43753557 | TAAA | T | 11 | a0001c0001t0003g0014 a0001c0001t0003g0015 a0001c0001t0003g0016 others(8): Show |
11 | HG02258.hp1 NA18612.hp2 NA18747.hp1 others(8): Show |
intron_variant | MODIFIER | c.208-475_208-473del others(3): Show |
HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr11 | 43753557 | ||||||
| chr11:43753627 | T | C | 2 | a0001c0001t0003g0206 a0002c0002t0002g0004 |
2 | HG03486.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.208-419T>C | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 2/10 | chr11 | 43753627 | |||||||
| chr11:43753815 | G | A | 1 | a0001c0001t0001g0082 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.208-231G>A | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 2/10 | chr11 | 43753815 | |||||||
| chr11:43753869 | A | C | 1 | a0002c0002t0008g0003 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.208-177A>C | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 2/10 | chr11 | 43753869 | |||||||
| chr11:43753970 | A | G | 1 | a0001c0001t0001g0076 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.208-76A>G | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 2/10 | chr11 | 43753970 | |||||||
| chr11:43754184 | A | G | 182 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(179): Show |
183 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(180): Show |
intron_variant | MODIFIER | c.283+63A>G | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 3/10 | chr11 | 43754184 | |||||||
| chr11:43754333 | G | A | 3 | a0001c0001t0001g0265 a0001c0001t0001g0266 a0001c0001t0001g0270 |
3 | HG02451.hp2 HG02630.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.283+212G>A | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 3/10 | chr11 | 43754333 | |||||||
| chr11:43754435 | G | A | 1 | a0002c0002t0002g0151 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.283+314G>A | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 3/10 | chr11 | 43754435 | |||||||
| chr11:43754538 | T | A | 1 | a0001c0003t0003g0243 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.283+417T>A | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 3/10 | chr11 | 43754538 | |||||||
| chr11:43754739 | A | C | 7 | a0001c0003t0003g0242 a0001c0003t0003g0243 a0001c0003t0003g0244 others(4): Show |
7 | HG01070.hp2 HG01071.hp1 HG02004.hp1 others(4): Show |
intron_variant | MODIFIER | c.283+618A>C | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 3/10 | chr11 | 43754739 | |||||||
| chr11:43754931 | C | T | 182 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(179): Show |
183 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(180): Show |
intron_variant | MODIFIER | c.283+810C>T | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 3/10 | chr11 | 43754931 | |||||||
| chr11:43755246 | G | A | 1 | a0002c0002t0008g0003 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.283+1125G>A | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 3/10 | chr11 | 43755246 | |||||||
| chr11:43755790 | G | A | 1 | a0001c0001t0001g0107 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.283+1669G>A | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 3/10 | chr11 | 43755790 | |||||||
| chr11:43755828 | G | A | 1 | a0001c0001t0001g0084 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.283+1707G>A | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 3/10 | chr11 | 43755828 | |||||||
| chr11:43755847 | G | A | 1 | a0001c0001t0001g0224 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.283+1726G>A | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 3/10 | chr11 | 43755847 | |||||||
| chr11:43755934 | G | A | 97 | a0001c0001t0001g0002 a0001c0001t0001g0026 a0001c0001t0001g0028 others(94): Show |
98 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(95): Show |
intron_variant | MODIFIER | c.283+1813G>A | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 3/10 | chr11 | 43755934 | |||||||
| chr11:43755950 | G | A | 1 | a0001c0001t0001g0099 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.283+1829G>A | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 3/10 | chr11 | 43755950 | |||||||
| chr11:43756179 | C | T | 2 | a0001c0003t0003g0244 a0001c0003t0003g0245 |
2 | HG02004.hp1 HG03239.hp2 |
intron_variant | MODIFIER | c.283+2058C>T | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 3/10 | chr11 | 43756179 | |||||||
| chr11:43756217 | CT | C | 16 | a0001c0001t0001g0255 a0001c0001t0003g0013 a0001c0001t0003g0014 others(13): Show |
16 | HG00280.hp1 HG00609.hp2 HG02258.hp1 others(13): Show |
intron_variant | MODIFIER | c.283+2109delT | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr11 | 43756217 | ||||||
| chr11:43756230 | T | A | 15 | a0001c0001t0001g0010 a0001c0001t0001g0100 a0001c0001t0003g0267 others(12): Show |
15 | HG01070.hp2 HG01071.hp1 HG02004.hp1 others(12): Show |
intron_variant | MODIFIER | c.283+2109T>A | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 3/10 | chr11 | 43756230 | |||||||
| chr11:43756670 | A | G | 2 | a0001c0003t0003g0231 a0001c0003t0003g0232 |
2 | HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.283+2549A>G | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 3/10 | chr11 | 43756670 | |||||||
| chr11:43757060 | T | C | 36 | a0001c0001t0001g0002 a0001c0001t0001g0111 a0001c0001t0001g0112 others(33): Show |
37 | HG00280.hp1 HG00609.hp2 HG01109.hp1 others(34): Show |
intron_variant | MODIFIER | c.283+2939T>C | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 3/10 | chr11 | 43757060 | |||||||
| chr11:43757315 | G | T | 1 | a0001c0001t0001g0032 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.283+3194G>T | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 3/10 | chr11 | 43757315 | |||||||
| chr11:43757572 | G | A | 2 | a0001c0001t0001g0262 a0001c0001t0001g0263 |
2 | HG02258.hp2 HG02280.hp1 |
intron_variant | MODIFIER | c.283+3451G>A | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 3/10 | chr11 | 43757572 | |||||||
| chr11:43757609 | C | T | 7 | a0001c0003t0003g0242 a0001c0003t0003g0243 a0001c0003t0003g0244 others(4): Show |
7 | HG01070.hp2 HG01071.hp1 HG02004.hp1 others(4): Show |
intron_variant | MODIFIER | c.283+3488C>T | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 3/10 | chr11 | 43757609 | |||||||
| chr11:43757627 | G | A | 19 | a0001c0001t0001g0128 a0001c0001t0001g0129 a0001c0001t0001g0265 others(16): Show |
19 | HG00639.hp2 HG00642.hp2 HG01069.hp1 others(16): Show |
intron_variant | MODIFIER | c.283+3506G>A | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 3/10 | chr11 | 43757627 | |||||||
| chr11:43757639 | C | CA | 72 | a0001c0001t0001g0026 a0001c0001t0001g0030 a0001c0001t0001g0036 others(69): Show |
72 | HG00323.hp1 HG00408.hp1 HG00423.hp2 others(69): Show |
intron_variant | MODIFIER | c.283+3546dupA | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr11 | 43757639 | ||||||
| chr11:43757639 | C | CAA | 47 | a0001c0001t0001g0052 a0001c0001t0001g0083 a0001c0001t0001g0107 others(44): Show |
48 | HG00140.hp2 HG00280.hp2 HG00408.hp2 others(45): Show |
intron_variant | MODIFIER | c.283+3545_283+3546d others(4): Show |
HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr11 | 43757639 | ||||||
| chr11:43757639 | C | CAAA | 14 | a0001c0001t0001g0257 a0001c0001t0001g0260 a0001c0001t0001g0263 others(11): Show |
14 | HG01099.hp1 HG01346.hp1 HG01358.hp1 others(11): Show |
intron_variant | MODIFIER | c.283+3544_283+3546d others(5): Show |
HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr11 | 43757639 | ||||||
| chr11:43757639 | C | CAAAA | 12 | a0001c0001t0001g0002 a0001c0001t0001g0120 a0001c0001t0001g0121 others(9): Show |
13 | HG00642.hp2 HG01496.hp1 HG02083.hp1 others(10): Show |
intron_variant | MODIFIER | c.283+3543_283+3546d others(6): Show |
HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr11 | 43757639 | ||||||
| chr11:43757639 | C | CAAAAA | 16 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0123 others(13): Show |
16 | HG00639.hp2 HG01069.hp1 HG01109.hp1 others(13): Show |
intron_variant | MODIFIER | c.283+3542_283+3546d others(7): Show |
HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr11 | 43757639 | ||||||
| chr11:43757639 | C | CAAAAAA | 15 | a0001c0001t0001g0009 a0001c0001t0001g0032 a0001c0001t0001g0033 others(12): Show |
15 | HG01106.hp1 HG01168.hp2 HG01261.hp1 others(12): Show |
intron_variant | MODIFIER | c.283+3541_283+3546d others(8): Show |
HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr11 | 43757639 | ||||||
| chr11:43757639 | C | CAAAAAAA | 9 | a0001c0001t0001g0005 a0001c0001t0001g0212 a0001c0001t0001g0214 others(6): Show |
9 | HG00099.hp2 HG01167.hp2 HG03540.hp1 others(6): Show |
intron_variant | MODIFIER | c.283+3540_283+3546d others(9): Show |
HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr11 | 43757639 | ||||||
| chr11:43757639 | C | CAAAAAAA others(1): Show |
10 | a0001c0001t0001g0208 a0001c0001t0001g0209 a0001c0001t0001g0210 others(7): Show |
10 | HG00140.hp1 HG02523.hp2 HG02717.hp2 others(7): Show |
intron_variant | MODIFIER | c.283+3539_283+3546d others(10): Show |
HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr11 | 43757639 | ||||||
| chr11:43757639 | C | CAAAAAAA others(4): Show |
1 | a0001c0001t0003g0206 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.283+3536_283+3546d others(13): Show |
HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr11 | 43757639 | ||||||
| chr11:43757639 | CAAAAAAA others(3): Show |
C | 1 | a0003c0004t0001g0241 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.283+3537_283+3546d others(12): Show |
HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr11 | 43757639 | ||||||
| chr11:43757643 | A | AACAAAAC others(5): Show |
1 | a0001c0007t0001g0230 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.283+3523_283+3524i others(14): Show |
HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr11 | 43757643 | ||||||
| chr11:43757646 | A | AAAACAAA others(7): Show |
1 | a0001c0001t0003g0023 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.283+3528_283+3529i others(16): Show |
HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr11 | 43757646 | ||||||
| chr11:43757648 | A | C | 1 | a0001c0007t0001g0230 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.283+3527A>C | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 3/10 | chr11 | 43757648 | |||||||
| chr11:43757651 | A | AAAACAAA others(7): Show |
13 | a0001c0001t0003g0013 a0001c0001t0003g0014 a0001c0001t0003g0015 others(10): Show |
13 | HG00609.hp2 NA18612.hp2 NA18747.hp1 others(10): Show |
intron_variant | MODIFIER | c.283+3533_283+3534i others(16): Show |
HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr11 | 43757651 | ||||||
| chr11:43757651 | A | C | 1 | a0001c0001t0003g0023 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.283+3530A>C | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 3/10 | chr11 | 43757651 | |||||||
| chr11:43757652 | A | C | 1 | a0001c0001t0001g0101 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.283+3531A>C | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 3/10 | chr11 | 43757652 | |||||||
| chr11:43757653 | A | C | 1 | a0001c0007t0001g0230 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.283+3532A>C | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 3/10 | chr11 | 43757653 | |||||||
| chr11:43757656 | A | C | 14 | a0001c0001t0003g0013 a0001c0001t0003g0014 a0001c0001t0003g0015 others(11): Show |
14 | HG00280.hp1 HG00609.hp2 NA18612.hp2 others(11): Show |
intron_variant | MODIFIER | c.283+3535A>C | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 3/10 | chr11 | 43757656 | |||||||
| chr11:43757658 | A | C | 1 | a0001c0007t0001g0230 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.283+3537A>C | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 3/10 | chr11 | 43757658 | |||||||
| chr11:43757661 | A | C | 14 | a0001c0001t0003g0013 a0001c0001t0003g0014 a0001c0001t0003g0015 others(11): Show |
14 | HG00280.hp1 HG00609.hp2 NA18612.hp2 others(11): Show |
intron_variant | MODIFIER | c.283+3540A>C | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 3/10 | chr11 | 43757661 | |||||||
| chr11:43757716 | C | CA | 51 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(48): Show |
52 | HG00099.hp2 HG00140.hp1 HG01109.hp1 others(49): Show |
intron_variant | MODIFIER | c.283+3603dupA | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr11 | 43757716 | ||||||
| chr11:43757717 | A | AC | 21 | a0001c0001t0001g0128 a0001c0001t0001g0129 a0001c0001t0001g0215 others(18): Show |
21 | HG00639.hp2 HG00642.hp2 HG01069.hp1 others(18): Show |
intron_variant | MODIFIER | c.283+3596_283+3597i others(3): Show |
HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 3/10 | chr11 | 43757717 | |||||||
| chr11:43757968 | G | A | 36 | a0001c0001t0001g0002 a0001c0001t0001g0111 a0001c0001t0001g0112 others(33): Show |
37 | HG00280.hp1 HG00609.hp2 HG01109.hp1 others(34): Show |
intron_variant | MODIFIER | c.283+3847G>A | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 3/10 | chr11 | 43757968 | |||||||
| chr11:43758044 | C | T | 36 | a0001c0001t0001g0002 a0001c0001t0001g0111 a0001c0001t0001g0112 others(33): Show |
37 | HG00280.hp1 HG00609.hp2 HG01109.hp1 others(34): Show |
intron_variant | MODIFIER | c.283+3923C>T | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 3/10 | chr11 | 43758044 | |||||||
| chr11:43758322 | G | A | 15 | a0001c0001t0003g0013 a0001c0001t0003g0014 a0001c0001t0003g0015 others(12): Show |
15 | HG00280.hp1 HG00609.hp2 HG02258.hp1 others(12): Show |
intron_variant | MODIFIER | c.283+4201G>A | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 3/10 | chr11 | 43758322 | |||||||
| chr11:43758470 | C | G | 5 | a0002c0002t0002g0161 a0002c0002t0002g0175 a0002c0002t0002g0176 others(2): Show |
5 | HG02647.hp1 HG02723.hp1 HG03130.hp2 others(2): Show |
intron_variant | MODIFIER | c.283+4349C>G | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 3/10 | chr11 | 43758470 | |||||||
| chr11:43758563 | G | A | 1 | a0001c0007t0001g0230 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.283+4442G>A | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 3/10 | chr11 | 43758563 | |||||||
| chr11:43758564 | G | A | 1 | a0001c0001t0001g0113 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.283+4443G>A | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 3/10 | chr11 | 43758564 | |||||||
| chr11:43758643 | G | A | 53 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(50): Show |
53 | HG00099.hp2 HG00140.hp1 HG00639.hp2 others(50): Show |
intron_variant | MODIFIER | c.283+4522G>A | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 3/10 | chr11 | 43758643 | |||||||
| chr11:43758728 | T | G | 5 | a0001c0001t0001g0111 a0001c0001t0001g0112 a0001c0001t0001g0202 others(2): Show |
5 | HG02055.hp1 HG02559.hp2 HG02809.hp2 others(2): Show |
intron_variant | MODIFIER | c.283+4607T>G | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 3/10 | chr11 | 43758728 | |||||||
| chr11:43758782 | A | G | 1 | a0001c0003t0001g0239 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.283+4661A>G | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 3/10 | chr11 | 43758782 | |||||||
| chr11:43758845 | A | G | 22 | a0002c0002t0002g0027 a0002c0002t0002g0109 a0002c0002t0002g0116 others(19): Show |
22 | HG00280.hp2 HG00423.hp1 HG00738.hp1 others(19): Show |
intron_variant | MODIFIER | c.283+4724A>G | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 3/10 | chr11 | 43758845 | |||||||
| chr11:43759003 | C | A | 183 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(180): Show |
184 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(181): Show |
intron_variant | MODIFIER | c.283+4882C>A | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 3/10 | chr11 | 43759003 | |||||||
| chr11:43759087 | A | G | 16 | a0001c0001t0001g0002 a0001c0001t0001g0120 a0001c0001t0001g0121 others(13): Show |
17 | HG01109.hp1 HG01496.hp1 HG02258.hp2 others(14): Show |
intron_variant | MODIFIER | c.283+4966A>G | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 3/10 | chr11 | 43759087 | |||||||
| chr11:43759423 | A | G | 1 | a0002c0002t0002g0004 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.283+5302A>G | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 3/10 | chr11 | 43759423 | |||||||
| chr11:43759516 | A | G | 1 | a0002c0002t0008g0003 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.283+5395A>G | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 3/10 | chr11 | 43759516 | |||||||
| chr11:43759525 | A | T | 2 | a0002c0002t0002g0163 a0002c0002t0002g0164 |
2 | HG02083.hp1 HG02165.hp1 |
intron_variant | MODIFIER | c.283+5404A>T | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 3/10 | chr11 | 43759525 | |||||||
| chr11:43759750 | CAG | C | 14 | a0001c0001t0003g0013 a0001c0001t0003g0014 a0001c0001t0003g0015 others(11): Show |
14 | HG00280.hp1 HG00609.hp2 NA18612.hp2 others(11): Show |
intron_variant | MODIFIER | c.283+5632_283+5633d others(4): Show |
HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr11 | 43759750 | ||||||
| chr11:43759886 | C | T | 1 | a0001c0003t0003g0245 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.283+5765C>T | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 3/10 | chr11 | 43759886 | |||||||
| chr11:43759909 | A | T | 2 | a0001c0001t0001g0009 a0001c0001t0001g0226 |
2 | HG01261.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.283+5788A>T | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 3/10 | chr11 | 43759909 | |||||||
| chr11:43759957 | A | G | 15 | a0001c0001t0003g0013 a0001c0001t0003g0014 a0001c0001t0003g0015 others(12): Show |
15 | HG00280.hp1 HG00609.hp2 HG02258.hp1 others(12): Show |
intron_variant | MODIFIER | c.283+5836A>G | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 3/10 | chr11 | 43759957 | |||||||
| chr11:43759959 | G | A | 14 | a0001c0001t0003g0013 a0001c0001t0003g0014 a0001c0001t0003g0015 others(11): Show |
14 | HG00280.hp1 HG00609.hp2 NA18612.hp2 others(11): Show |
intron_variant | MODIFIER | c.283+5838G>A | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 3/10 | chr11 | 43759959 | |||||||
| chr11:43760109 | G | A | 3 | a0003c0004t0001g0241 a0003c0004t0001g0249 a0003c0004t0001g0264 |
3 | HG02647.hp2 HG03516.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.283+5988G>A | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 3/10 | chr11 | 43760109 | |||||||
| chr11:43760201 | T | A | 1 | a0002c0002t0002g0039 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.283+6080T>A | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 3/10 | chr11 | 43760201 | |||||||
| chr11:43760231 | G | A | 5 | a0002c0002t0002g0161 a0002c0002t0002g0175 a0002c0002t0002g0176 others(2): Show |
5 | HG02647.hp1 HG02723.hp1 HG03130.hp2 others(2): Show |
intron_variant | MODIFIER | c.283+6110G>A | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 3/10 | chr11 | 43760231 | |||||||
| chr11:43760308 | C | A | 14 | a0001c0001t0003g0013 a0001c0001t0003g0014 a0001c0001t0003g0015 others(11): Show |
14 | HG00280.hp1 HG00609.hp2 NA18612.hp2 others(11): Show |
intron_variant | MODIFIER | c.283+6187C>A | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 3/10 | chr11 | 43760308 | |||||||
| chr11:43760324 | A | G | 1 | a0002c0002t0008g0003 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.283+6203A>G | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 3/10 | chr11 | 43760324 | |||||||
| chr11:43760540 | A | G | 1 | a0001c0001t0001g0096 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.283+6419A>G | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 3/10 | chr11 | 43760540 | |||||||
| chr11:43760926 | G | T | 1 | a0002c0002t0002g0139 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.283+6805G>T | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 3/10 | chr11 | 43760926 | |||||||
| chr11:43761078 | T | TAGTC | 26 | a0001c0001t0001g0009 a0001c0001t0001g0087 a0001c0001t0001g0128 others(23): Show |
26 | HG00099.hp2 HG00140.hp1 HG01167.hp2 others(23): Show |
intron_variant | MODIFIER | c.283+6958_283+6961d others(6): Show |
HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr11 | 43761078 | ||||||
| chr11:43761151 | T | C | 21 | a0001c0001t0001g0002 a0001c0001t0001g0111 a0001c0001t0001g0112 others(18): Show |
22 | HG01109.hp1 HG01496.hp1 HG02055.hp1 others(19): Show |
intron_variant | MODIFIER | c.283+7030T>C | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 3/10 | chr11 | 43761151 | |||||||
| chr11:43761174 | T | C | 1 | a0001c0003t0001g0229 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.283+7053T>C | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 3/10 | chr11 | 43761174 | |||||||
| chr11:43761417 | A | C | 8 | a0002c0002t0002g0004 a0002c0002t0002g0144 a0002c0002t0002g0145 others(5): Show |
8 | HG01884.hp1 HG02622.hp1 HG02630.hp2 others(5): Show |
intron_variant | MODIFIER | c.283+7296A>C | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 3/10 | chr11 | 43761417 | |||||||
| chr11:43761485 | A | C | 6 | a0002c0002t0002g0004 a0002c0002t0002g0145 a0002c0002t0002g0153 others(3): Show |
6 | HG02622.hp1 HG02630.hp2 HG02717.hp1 others(3): Show |
intron_variant | MODIFIER | c.283+7364A>C | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 3/10 | chr11 | 43761485 | |||||||
| chr11:43761574 | T | C | 14 | a0001c0001t0003g0013 a0001c0001t0003g0014 a0001c0001t0003g0015 others(11): Show |
14 | HG00280.hp1 HG00609.hp2 NA18612.hp2 others(11): Show |
intron_variant | MODIFIER | c.283+7453T>C | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 3/10 | chr11 | 43761574 | |||||||
| chr11:43761595 | G | A | 1 | a0002c0002t0002g0155 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.283+7474G>A | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 3/10 | chr11 | 43761595 | |||||||
| chr11:43761732 | C | G | 38 | a0002c0002t0002g0004 a0002c0002t0002g0027 a0002c0002t0002g0109 others(35): Show |
38 | HG00280.hp2 HG00423.hp1 HG00738.hp1 others(35): Show |
intron_variant | MODIFIER | c.283+7611C>G | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 3/10 | chr11 | 43761732 | |||||||
| chr11:43761874 | C | T | 10 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(7): Show |
10 | HG01884.hp2 HG02257.hp1 HG02717.hp2 others(7): Show |
intron_variant | MODIFIER | c.283+7753C>T | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 3/10 | chr11 | 43761874 | |||||||
| chr11:43761901 | C | CTTTAAGT others(6): Show |
1 | a0001c0007t0001g0230 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.283+7780_283+7781i others(15): Show |
HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 3/10 | chr11 | 43761901 | |||||||
| chr11:43761902 | C | T | 1 | a0001c0007t0001g0230 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.283+7781C>T | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 3/10 | chr11 | 43761902 | |||||||
| chr11:43762178 | G | GA | 77 | a0001c0001t0001g0026 a0001c0001t0001g0028 a0001c0001t0001g0029 others(74): Show |
77 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(74): Show |
intron_variant | MODIFIER | c.283+8065dupA | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr11 | 43762178 | ||||||
| chr11:43762184 | A | G | 21 | a0001c0001t0001g0002 a0001c0001t0001g0111 a0001c0001t0001g0112 others(18): Show |
22 | HG01109.hp1 HG01496.hp1 HG02055.hp1 others(19): Show |
intron_variant | MODIFIER | c.283+8063A>G | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 3/10 | chr11 | 43762184 | |||||||
| chr11:43762429 | T | C | 7 | a0001c0001t0001g0005 a0001c0001t0001g0007 a0001c0001t0001g0008 others(4): Show |
7 | HG01884.hp2 HG02809.hp1 HG02886.hp2 others(4): Show |
intron_variant | MODIFIER | c.283+8308T>C | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 3/10 | chr11 | 43762429 | |||||||
| chr11:43762454 | C | T | 1 | a0001c0001t0003g0013 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.283+8333C>T | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 3/10 | chr11 | 43762454 | |||||||
| chr11:43762718 | C | T | 1 | a0001c0001t0001g0105 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.283+8597C>T | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 3/10 | chr11 | 43762718 | |||||||
| chr11:43762788 | G | A | 1 | a0001c0007t0001g0230 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.283+8667G>A | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 3/10 | chr11 | 43762788 | |||||||
| chr11:43763001 | A | T | 1 | a0001c0001t0001g0040 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.283+8880A>T | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 3/10 | chr11 | 43763001 | |||||||
| chr11:43763086 | G | A | 53 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(50): Show |
53 | HG00099.hp2 HG00140.hp1 HG00639.hp2 others(50): Show |
intron_variant | MODIFIER | c.283+8965G>A | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 3/10 | chr11 | 43763086 | |||||||
| chr11:43763586 | T | TTA | 59 | a0001c0001t0001g0009 a0001c0001t0001g0056 a0001c0001t0001g0059 others(56): Show |
59 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(56): Show |
intron_variant | MODIFIER | c.283+9480_283+9481d others(4): Show |
HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr11 | 43763586 | ||||||
| chr11:43763586 | T | TTATA | 9 | a0001c0001t0001g0005 a0001c0001t0001g0007 a0001c0001t0001g0008 others(6): Show |
9 | HG01884.hp2 HG02257.hp1 HG02717.hp2 others(6): Show |
intron_variant | MODIFIER | c.283+9478_283+9481d others(6): Show |
HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr11 | 43763586 | ||||||
| chr11:43763588 | A | G | 27 | a0002c0002t0002g0027 a0002c0002t0002g0109 a0002c0002t0002g0116 others(24): Show |
27 | HG00280.hp2 HG00423.hp1 HG00738.hp1 others(24): Show |
intron_variant | MODIFIER | c.283+9467A>G | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 3/10 | chr11 | 43763588 | |||||||
| chr11:43763611 | T | TTA | 60 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(57): Show |
61 | HG00099.hp2 HG00140.hp1 HG00639.hp2 others(58): Show |
intron_variant | MODIFIER | c.283+9504_283+9505d others(4): Show |
HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr11 | 43763611 | ||||||
| chr11:43763613 | A | G | 15 | a0001c0001t0003g0013 a0001c0001t0003g0014 a0001c0001t0003g0015 others(12): Show |
15 | HG00280.hp1 HG00609.hp2 HG02258.hp1 others(12): Show |
intron_variant | MODIFIER | c.283+9492A>G | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 3/10 | chr11 | 43763613 | |||||||
| chr11:43763625 | A | C | 1 | a0002c0002t0008g0003 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.283+9504A>C | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 3/10 | chr11 | 43763625 | |||||||
| chr11:43763654 | G | T | 226 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(223): Show |
228 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(225): Show |
intron_variant | MODIFIER | c.283+9533G>T | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 3/10 | chr11 | 43763654 | |||||||
| chr11:43763656 | G | T | 42 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0009 others(39): Show |
42 | HG00099.hp2 HG00140.hp1 HG00609.hp2 others(39): Show |
intron_variant | MODIFIER | c.283+9535G>T | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 3/10 | chr11 | 43763656 | |||||||
| chr11:43763658 | G | T | 2 | a0001c0001t0001g0125 a0002c0002t0009g0200 |
2 | HG01884.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.283+9537G>T | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 3/10 | chr11 | 43763658 | |||||||
| chr11:43763944 | C | T | 15 | a0001c0001t0003g0013 a0001c0001t0003g0014 a0001c0001t0003g0015 others(12): Show |
15 | HG00280.hp1 HG00609.hp2 HG02258.hp1 others(12): Show |
intron_variant | MODIFIER | c.283+9823C>T | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 3/10 | chr11 | 43763944 | |||||||
| chr11:43763980 | G | A | 7 | a0001c0003t0003g0242 a0001c0003t0003g0243 a0001c0003t0003g0244 others(4): Show |
7 | HG01070.hp2 HG01071.hp1 HG02004.hp1 others(4): Show |
intron_variant | MODIFIER | c.283+9859G>A | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 3/10 | chr11 | 43763980 | |||||||
| chr11:43764117 | T | A | 1 | a0001c0001t0001g0224 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.283+9996T>A | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 3/10 | chr11 | 43764117 | |||||||
| chr11:43764118 | A | T | 1 | a0001c0001t0001g0224 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.283+9997A>T | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 3/10 | chr11 | 43764118 | |||||||
| chr11:43764169 | C | G | 1 | a0002c0002t0002g0184 | 1 | NA19001.hp1 | intron_variant | MODIFIER | c.283+10048C>G | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 3/10 | chr11 | 43764169 | |||||||
| chr11:43764173 | T | C | 1 | a0001c0001t0001g0152 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.283+10052T>C | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 3/10 | chr11 | 43764173 | |||||||
| chr11:43764183 | A | C | 182 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(179): Show |
183 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(180): Show |
intron_variant | MODIFIER | c.283+10062A>C | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 3/10 | chr11 | 43764183 | |||||||
| chr11:43764682 | T | C | 1 | a0002c0002t0009g0200 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.283+10561T>C | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 3/10 | chr11 | 43764682 | |||||||
| chr11:43764714 | A | C | 1 | a0001c0001t0001g0186 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.283+10593A>C | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 3/10 | chr11 | 43764714 | |||||||
| chr11:43764763 | A | G | 183 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(180): Show |
184 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(181): Show |
intron_variant | MODIFIER | c.283+10642A>G | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 3/10 | chr11 | 43764763 | |||||||
| chr11:43764841 | C | T | 1 | a0001c0001t0001g0054 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.283+10720C>T | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 3/10 | chr11 | 43764841 | |||||||
| chr11:43764880 | G | A | 1 | a0002c0002t0009g0200 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.283+10759G>A | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 3/10 | chr11 | 43764880 | |||||||
| chr11:43764929 | C | T | 53 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(50): Show |
53 | HG00099.hp2 HG00140.hp1 HG00639.hp2 others(50): Show |
intron_variant | MODIFIER | c.283+10808C>T | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 3/10 | chr11 | 43764929 | |||||||
| chr11:43765004 | G | GGATT | 182 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(179): Show |
183 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(180): Show |
intron_variant | MODIFIER | c.283+10883_283+1088 others(8): Show |
HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 3/10 | chr11 | 43765004 | |||||||
| chr11:43765011 | A | T | 4 | a0001c0001t0001g0060 a0001c0001t0001g0061 a0001c0001t0001g0062 others(1): Show |
4 | HG02300.hp2 HG03453.hp2 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.283+10890A>T | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 3/10 | chr11 | 43765011 | |||||||
| chr11:43765563 | C | T | 3 | a0001c0001t0001g0060 a0001c0001t0001g0061 a0001c0001t0001g0062 |
3 | HG03453.hp2 HG03471.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.283+11442C>T | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 3/10 | chr11 | 43765563 | |||||||
| chr11:43765725 | C | T | 2 | a0001c0001t0001g0069 a0001c0001t0001g0105 |
2 | HG01928.hp1 NA19000.hp2 |
intron_variant | MODIFIER | c.283+11604C>T | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 3/10 | chr11 | 43765725 | |||||||
| chr11:43765880 | A | C | 17 | a0001c0001t0001g0092 a0001c0001t0001g0094 a0001c0001t0003g0013 others(14): Show |
17 | HG00280.hp1 HG00609.hp2 HG02258.hp1 others(14): Show |
intron_variant | MODIFIER | c.283+11759A>C | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 3/10 | chr11 | 43765880 | |||||||
| chr11:43765958 | C | T | 1 | a0002c0002t0008g0003 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.283+11837C>T | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 3/10 | chr11 | 43765958 | |||||||
| chr11:43765971 | G | A | 53 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(50): Show |
53 | HG00099.hp2 HG00140.hp1 HG00639.hp2 others(50): Show |
intron_variant | MODIFIER | c.283+11850G>A | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 3/10 | chr11 | 43765971 | |||||||
| chr11:43765986 | C | T | 10 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(7): Show |
10 | HG01884.hp2 HG02257.hp1 HG02717.hp2 others(7): Show |
intron_variant | MODIFIER | c.283+11865C>T | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 3/10 | chr11 | 43765986 | |||||||
| chr11:43766015 | C | T | 16 | a0001c0001t0001g0092 a0001c0001t0001g0094 a0001c0001t0003g0013 others(13): Show |
16 | HG00280.hp1 HG00609.hp2 NA18612.hp2 others(13): Show |
intron_variant | MODIFIER | c.283+11894C>T | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 3/10 | chr11 | 43766015 | |||||||
| chr11:43766105 | G | A | 1 | a0002c0002t0002g0175 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.283+11984G>A | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 3/10 | chr11 | 43766105 | |||||||
| chr11:43766115 | G | A | 2 | a0002c0002t0004g0205 a0002c0002t0004g0274 |
2 | HG02451.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.283+11994G>A | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 3/10 | chr11 | 43766115 | |||||||
| chr11:43766124 | C | T | 19 | a0001c0001t0001g0128 a0001c0001t0001g0129 a0001c0001t0001g0265 others(16): Show |
19 | HG00639.hp2 HG00642.hp2 HG01069.hp1 others(16): Show |
intron_variant | MODIFIER | c.283+12003C>T | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 3/10 | chr11 | 43766124 | |||||||
| chr11:43766154 | G | A | 1 | a0001c0001t0001g0195 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.283+12033G>A | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 3/10 | chr11 | 43766154 | |||||||
| chr11:43766225 | C | CAATTAGT others(8): Show |
2 | a0001c0003t0003g0231 a0001c0003t0003g0232 |
2 | HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.283+12116_283+1213 others(19): Show |
HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr11 | 43766225 | ||||||
| chr11:43766258 | G | T | 2 | a0001c0003t0003g0231 a0001c0003t0003g0232 |
2 | HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.283+12137G>T | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 3/10 | chr11 | 43766258 | |||||||
| chr11:43766284 | C | T | 7 | a0001c0003t0003g0242 a0001c0003t0003g0243 a0001c0003t0003g0244 others(4): Show |
7 | HG01070.hp2 HG01071.hp1 HG02004.hp1 others(4): Show |
intron_variant | MODIFIER | c.283+12163C>T | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 3/10 | chr11 | 43766284 | |||||||
| chr11:43766300 | T | C | 21 | a0001c0001t0001g0060 a0001c0001t0001g0061 a0001c0001t0001g0062 others(18): Show |
21 | HG00280.hp1 HG00609.hp2 HG02258.hp1 others(18): Show |
intron_variant | MODIFIER | c.283+12179T>C | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 3/10 | chr11 | 43766300 | |||||||
| chr11:43766390 | A | G | 17 | a0001c0001t0001g0092 a0001c0001t0001g0094 a0001c0001t0003g0013 others(14): Show |
17 | HG00280.hp1 HG00609.hp2 HG02258.hp1 others(14): Show |
intron_variant | MODIFIER | c.283+12269A>G | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 3/10 | chr11 | 43766390 | |||||||
| chr11:43766470 | A | T | 2 | a0001c0003t0003g0231 a0001c0003t0003g0232 |
2 | HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.283+12349A>T | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 3/10 | chr11 | 43766470 | |||||||
| chr11:43766780 | T | C | 112 | a0001c0001t0001g0002 a0001c0001t0001g0026 a0001c0001t0001g0028 others(109): Show |
113 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(110): Show |
intron_variant | MODIFIER | c.283+12659T>C | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 3/10 | chr11 | 43766780 | |||||||
| chr11:43766811 | G | T | 21 | a0001c0001t0001g0002 a0001c0001t0001g0111 a0001c0001t0001g0112 others(18): Show |
22 | HG01109.hp1 HG01496.hp1 HG02055.hp1 others(19): Show |
intron_variant | MODIFIER | c.283+12690G>T | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 3/10 | chr11 | 43766811 | |||||||
| chr11:43766909 | C | T | 1 | a0001c0003t0001g0229 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.283+12788C>T | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 3/10 | chr11 | 43766909 | |||||||
| chr11:43767117 | C | T | 17 | a0001c0001t0003g0267 a0001c0001t0003g0268 a0001c0001t0003g0278 others(14): Show |
17 | HG01070.hp2 HG01071.hp1 HG02004.hp1 others(14): Show |
intron_variant | MODIFIER | c.283+12996C>T | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 3/10 | chr11 | 43767117 | |||||||
| chr11:43767121 | A | G | 7 | a0001c0003t0003g0242 a0001c0003t0003g0243 a0001c0003t0003g0244 others(4): Show |
7 | HG01070.hp2 HG01071.hp1 HG02004.hp1 others(4): Show |
intron_variant | MODIFIER | c.283+13000A>G | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 3/10 | chr11 | 43767121 | |||||||
| chr11:43767127 | G | T | 1 | a0001c0001t0001g0026 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.283+13006G>T | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 3/10 | chr11 | 43767127 | |||||||
| chr11:43767204 | T | TA | 77 | a0001c0001t0001g0026 a0001c0001t0001g0028 a0001c0001t0001g0029 others(74): Show |
77 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(74): Show |
intron_variant | MODIFIER | c.283+13095dupA | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr11 | 43767204 | ||||||
| chr11:43767214 | A | AC | 14 | a0001c0001t0001g0002 a0001c0001t0001g0120 a0001c0001t0001g0121 others(11): Show |
15 | HG01109.hp1 HG01496.hp1 HG02258.hp2 others(12): Show |
intron_variant | MODIFIER | c.283+13093_283+1309 others(5): Show |
HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 3/10 | chr11 | 43767214 | |||||||
| chr11:43767215 | A | C | 13 | a0001c0001t0003g0267 a0001c0001t0003g0268 a0001c0001t0003g0278 others(10): Show |
13 | HG01070.hp2 HG01071.hp1 HG02004.hp1 others(10): Show |
intron_variant | MODIFIER | c.283+13094A>C | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 3/10 | chr11 | 43767215 | |||||||
| chr11:43767672 | A | G | 182 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(179): Show |
183 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(180): Show |
intron_variant | MODIFIER | c.283+13551A>G | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 3/10 | chr11 | 43767672 | |||||||
| chr11:43768100 | T | G | 3 | a0002c0002t0002g0192 a0002c0002t0002g0193 a0002c0002t0002g0194 |
3 | HG02559.hp1 HG03516.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.283+13979T>G | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 3/10 | chr11 | 43768100 | |||||||
| chr11:43768122 | C | T | 3 | a0001c0001t0001g0034 a0001c0001t0001g0071 a0001c0001t0001g0100 |
3 | NA18612.hp1 NA18945.hp2 NA18982.hp1 |
intron_variant | MODIFIER | c.283+14001C>T | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 3/10 | chr11 | 43768122 | |||||||
| chr11:43768140 | A | G | 1 | a0002c0002t0002g0127 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.283+14019A>G | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 3/10 | chr11 | 43768140 | |||||||
| chr11:43768288 | G | A | 15 | a0001c0001t0003g0013 a0001c0001t0003g0014 a0001c0001t0003g0015 others(12): Show |
15 | HG00280.hp1 HG00609.hp2 HG02258.hp1 others(12): Show |
intron_variant | MODIFIER | c.283+14167G>A | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 3/10 | chr11 | 43768288 | |||||||
| chr11:43768373 | G | C | 1 | a0001c0001t0001g0260 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.283+14252G>C | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 3/10 | chr11 | 43768373 | |||||||
| chr11:43768394 | C | T | 17 | a0001c0001t0003g0267 a0001c0001t0003g0268 a0001c0001t0003g0278 others(14): Show |
17 | HG01070.hp2 HG01071.hp1 HG02004.hp1 others(14): Show |
intron_variant | MODIFIER | c.283+14273C>T | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 3/10 | chr11 | 43768394 | |||||||
| chr11:43768440 | T | C | 1 | a0002c0002t0002g0170 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.283+14319T>C | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 3/10 | chr11 | 43768440 | |||||||
| chr11:43768491 | C | T | 3 | a0001c0001t0001g0005 a0001c0001t0001g0007 a0001c0001t0001g0008 |
3 | HG02809.hp1 HG02886.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.283+14370C>T | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 3/10 | chr11 | 43768491 | |||||||
| chr11:43768519 | G | C | 19 | a0001c0001t0001g0060 a0001c0001t0001g0061 a0001c0001t0001g0062 others(16): Show |
19 | HG00280.hp1 HG00609.hp2 HG02258.hp1 others(16): Show |
intron_variant | MODIFIER | c.283+14398G>C | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 3/10 | chr11 | 43768519 | |||||||
| chr11:43768582 | G | A | 4 | a0001c0001t0001g0221 a0001c0001t0001g0222 a0001c0001t0001g0223 others(1): Show |
4 | HG02602.hp1 HG03834.hp2 HG03942.hp1 others(1): Show |
intron_variant | MODIFIER | c.283+14461G>A | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 3/10 | chr11 | 43768582 | |||||||
| chr11:43768633 | T | C | 4 | a0001c0001t0001g0060 a0001c0001t0001g0061 a0001c0001t0001g0062 others(1): Show |
4 | HG02300.hp2 HG03453.hp2 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.283+14512T>C | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 3/10 | chr11 | 43768633 | |||||||
| chr11:43768652 | T | C | 8 | a0001c0001t0001g0074 a0001c0001t0001g0076 a0001c0001t0001g0083 others(5): Show |
8 | HG02083.hp2 HG02698.hp2 NA18944.hp1 others(5): Show |
intron_variant | MODIFIER | c.283+14531T>C | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 3/10 | chr11 | 43768652 | |||||||
| chr11:43768656 | A | T | 3 | a0002c0002t0004g0205 a0002c0002t0004g0274 a0002c0002t0009g0200 |
3 | HG02451.hp1 HG02970.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.283+14535A>T | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 3/10 | chr11 | 43768656 | |||||||
| chr11:43768760 | G | C | 1 | a0002c0002t0002g0180 | 1 | HG01258.hp1 | intron_variant | MODIFIER | c.283+14639G>C | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 3/10 | chr11 | 43768760 | |||||||
| chr11:43768764 | G | T | 3 | a0001c0003t0001g0225 a0001c0003t0001g0227 a0001c0003t0001g0272 |
3 | HG00140.hp1 HG01167.hp2 NA20752.hp2 |
intron_variant | MODIFIER | c.283+14643G>T | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 3/10 | chr11 | 43768764 | |||||||
| chr11:43768772 | G | A | 53 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(50): Show |
53 | HG00099.hp2 HG00140.hp1 HG00639.hp2 others(50): Show |
intron_variant | MODIFIER | c.283+14651G>A | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 3/10 | chr11 | 43768772 | |||||||
| chr11:43768784 | G | C | 9 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(6): Show |
9 | HG01884.hp2 HG02257.hp1 HG02809.hp1 others(6): Show |
intron_variant | MODIFIER | c.283+14663G>C | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 3/10 | chr11 | 43768784 | |||||||
| chr11:43768815 | C | T | 5 | a0001c0001t0001g0111 a0001c0001t0001g0112 a0001c0001t0001g0202 others(2): Show |
5 | HG02055.hp1 HG02559.hp2 HG02809.hp2 others(2): Show |
intron_variant | MODIFIER | c.283+14694C>T | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 3/10 | chr11 | 43768815 | |||||||
| chr11:43768825 | CTGCTGAT others(17): Show |
C | 19 | a0001c0001t0001g0060 a0001c0001t0001g0061 a0001c0001t0001g0062 others(16): Show |
19 | HG00280.hp1 HG00609.hp2 HG02258.hp1 others(16): Show |
intron_variant | MODIFIER | c.283+14724_283+1474 others(28): Show |
HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr11 | 43768825 | ||||||
| chr11:43769218 | G | T | 21 | a0001c0001t0001g0002 a0001c0001t0001g0111 a0001c0001t0001g0112 others(18): Show |
22 | HG01109.hp1 HG01496.hp1 HG02055.hp1 others(19): Show |
intron_variant | MODIFIER | c.283+15097G>T | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 3/10 | chr11 | 43769218 | |||||||
| chr11:43769430 | A | G | 16 | a0001c0001t0001g0002 a0001c0001t0001g0120 a0001c0001t0001g0121 others(13): Show |
17 | HG01109.hp1 HG01496.hp1 HG02258.hp2 others(14): Show |
intron_variant | MODIFIER | c.283+15309A>G | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 3/10 | chr11 | 43769430 | |||||||
| chr11:43769579 | C | G | 1 | a0002c0002t0008g0003 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.283+15458C>G | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 3/10 | chr11 | 43769579 | |||||||
| chr11:43769643 | A | T | 15 | a0001c0001t0003g0013 a0001c0001t0003g0014 a0001c0001t0003g0015 others(12): Show |
15 | HG00280.hp1 HG00609.hp2 HG02258.hp1 others(12): Show |
intron_variant | MODIFIER | c.283+15522A>T | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 3/10 | chr11 | 43769643 | |||||||
| chr11:43769697 | G | A | 1 | a0001c0001t0003g0024 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.283+15576G>A | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 3/10 | chr11 | 43769697 | |||||||
| chr11:43769716 | C | T | 12 | a0002c0002t0002g0027 a0002c0002t0002g0132 a0002c0002t0002g0133 others(9): Show |
12 | HG00280.hp2 HG00738.hp1 HG01099.hp1 others(9): Show |
intron_variant | MODIFIER | c.283+15595C>T | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 3/10 | chr11 | 43769716 | |||||||
| chr11:43769907 | A | G | 1 | a0001c0001t0001g0257 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.283+15786A>G | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 3/10 | chr11 | 43769907 | |||||||
| chr11:43770259 | C | T | 1 | a0002c0002t0002g0181 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.283+16138C>T | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 3/10 | chr11 | 43770259 | |||||||
| chr11:43770315 | G | A | 93 | a0001c0001t0001g0026 a0001c0001t0001g0028 a0001c0001t0001g0029 others(90): Show |
93 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(90): Show |
intron_variant | MODIFIER | c.283+16194G>A | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 3/10 | chr11 | 43770315 | |||||||
| chr11:43770486 | A | T | 1 | a0001c0001t0001g0186 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.283+16365A>T | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 3/10 | chr11 | 43770486 | |||||||
| chr11:43770497 | G | A | 1 | a0001c0007t0001g0230 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.283+16376G>A | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 3/10 | chr11 | 43770497 | |||||||
| chr11:43770578 | G | A | 36 | a0001c0001t0001g0002 a0001c0001t0001g0111 a0001c0001t0001g0112 others(33): Show |
37 | HG00280.hp1 HG00609.hp2 HG01109.hp1 others(34): Show |
intron_variant | MODIFIER | c.283+16457G>A | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 3/10 | chr11 | 43770578 | |||||||
| chr11:43770588 | C | T | 21 | a0001c0001t0001g0002 a0001c0001t0001g0111 a0001c0001t0001g0112 others(18): Show |
22 | HG01109.hp1 HG01496.hp1 HG02055.hp1 others(19): Show |
intron_variant | MODIFIER | c.283+16467C>T | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 3/10 | chr11 | 43770588 | |||||||
| chr11:43770598 | T | C | 21 | a0001c0001t0001g0002 a0001c0001t0001g0111 a0001c0001t0001g0112 others(18): Show |
22 | HG01109.hp1 HG01496.hp1 HG02055.hp1 others(19): Show |
intron_variant | MODIFIER | c.283+16477T>C | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 3/10 | chr11 | 43770598 | |||||||
| chr11:43770608 | C | T | 14 | a0001c0001t0003g0013 a0001c0001t0003g0014 a0001c0001t0003g0015 others(11): Show |
14 | HG00280.hp1 HG00609.hp2 NA18612.hp2 others(11): Show |
intron_variant | MODIFIER | c.283+16487C>T | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 3/10 | chr11 | 43770608 | |||||||
| chr11:43770630 | G | A | 1 | a0002c0002t0002g0165 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.283+16509G>A | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 3/10 | chr11 | 43770630 | |||||||
| chr11:43771003 | G | A | 1 | a0001c0001t0003g0206 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.283+16882G>A | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 3/10 | chr11 | 43771003 | |||||||
| chr11:43771071 | C | T | 1 | a0001c0001t0001g0073 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.283+16950C>T | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 3/10 | chr11 | 43771071 | |||||||
| chr11:43771311 | C | G | 5 | a0001c0001t0001g0209 a0001c0001t0001g0210 a0001c0001t0001g0211 others(2): Show |
5 | NA18966.hp2 NA18971.hp1 NA18973.hp1 others(2): Show |
intron_variant | MODIFIER | c.283+17190C>G | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 3/10 | chr11 | 43771311 | |||||||
| chr11:43771462 | C | CT | 142 | a0001c0001t0001g0002 a0001c0001t0001g0009 a0001c0001t0001g0026 others(139): Show |
143 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(140): Show |
intron_variant | MODIFIER | c.283+17363dupT | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr11 | 43771462 | ||||||
| chr11:43771462 | C | CTT | 22 | a0001c0001t0001g0006 a0001c0001t0001g0010 a0001c0001t0001g0032 others(19): Show |
22 | HG00639.hp2 HG01070.hp2 HG01071.hp1 others(19): Show |
intron_variant | MODIFIER | c.283+17362_283+1736 others(6): Show |
HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr11 | 43771462 | ||||||
| chr11:43771462 | CT | C | 16 | a0001c0001t0003g0014 a0001c0001t0003g0015 a0001c0001t0003g0016 others(13): Show |
16 | HG00609.hp2 HG00738.hp1 HG02258.hp1 others(13): Show |
intron_variant | MODIFIER | c.283+17363delT | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr11 | 43771462 | ||||||
| chr11:43771508 | C | T | 15 | a0001c0001t0003g0013 a0001c0001t0003g0014 a0001c0001t0003g0015 others(12): Show |
15 | HG00280.hp1 HG00609.hp2 HG02258.hp1 others(12): Show |
intron_variant | MODIFIER | c.283+17387C>T | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 3/10 | chr11 | 43771508 | |||||||
| chr11:43771611 | C | T | 1 | a0001c0001t0001g0271 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.283+17490C>T | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 3/10 | chr11 | 43771611 | |||||||
| chr11:43772023 | CAT | C | 182 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(179): Show |
183 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(180): Show |
intron_variant | MODIFIER | c.283+17915_283+1791 others(6): Show |
HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr11 | 43772023 | ||||||
| chr11:43772249 | A | G | 93 | a0001c0001t0001g0002 a0001c0001t0001g0026 a0001c0001t0001g0028 others(90): Show |
94 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(91): Show |
intron_variant | MODIFIER | c.283+18128A>G | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 3/10 | chr11 | 43772249 | |||||||
| chr11:43772274 | C | T | 1 | a0002c0002t0002g0038 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.283+18153C>T | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 3/10 | chr11 | 43772274 | |||||||
| chr11:43772533 | T | C | 1 | a0001c0001t0001g0186 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.283+18412T>C | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 3/10 | chr11 | 43772533 | |||||||
| chr11:43772813 | A | G | 1 | a0001c0001t0001g0254 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.283+18692A>G | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 3/10 | chr11 | 43772813 | |||||||
| chr11:43772829 | A | G | 112 | a0001c0001t0001g0002 a0001c0001t0001g0026 a0001c0001t0001g0028 others(109): Show |
113 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(110): Show |
intron_variant | MODIFIER | c.283+18708A>G | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 3/10 | chr11 | 43772829 | |||||||
| chr11:43772902 | G | C | 1 | a0001c0001t0001g0219 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.283+18781G>C | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 3/10 | chr11 | 43772902 | |||||||
| chr11:43772920 | G | A | 23 | a0001c0001t0001g0009 a0001c0001t0001g0186 a0001c0001t0001g0208 others(20): Show |
23 | HG00099.hp2 HG00140.hp1 HG01167.hp2 others(20): Show |
intron_variant | MODIFIER | c.283+18799G>A | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 3/10 | chr11 | 43772920 | |||||||
| chr11:43772974 | G | A | 1 | a0002c0002t0002g0193 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.283+18853G>A | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 3/10 | chr11 | 43772974 | |||||||
| chr11:43773042 | T | C | 182 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(179): Show |
183 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(180): Show |
intron_variant | MODIFIER | c.283+18921T>C | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 3/10 | chr11 | 43773042 | |||||||
| chr11:43773043 | G | A | 1 | a0002c0002t0009g0200 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.283+18922G>A | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 3/10 | chr11 | 43773043 | |||||||
| chr11:43773067 | C | T | 14 | a0001c0001t0003g0013 a0001c0001t0003g0014 a0001c0001t0003g0015 others(11): Show |
14 | HG00280.hp1 HG00609.hp2 NA18612.hp2 others(11): Show |
intron_variant | MODIFIER | c.283+18946C>T | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 3/10 | chr11 | 43773067 | |||||||
| chr11:43773340 | C | T | 2 | a0001c0001t0001g0006 a0001c0001t0001g0010 |
2 | HG02257.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.283+19219C>T | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 3/10 | chr11 | 43773340 | |||||||
| chr11:43773870 | T | C | 94 | a0001c0001t0001g0026 a0001c0001t0001g0028 a0001c0001t0001g0029 others(91): Show |
94 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(91): Show |
intron_variant | MODIFIER | c.283+19749T>C | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 3/10 | chr11 | 43773870 | |||||||
| chr11:43773944 | A | G | 1 | a0002c0002t0005g0207 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.283+19823A>G | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 3/10 | chr11 | 43773944 | |||||||
| chr11:43773993 | A | G | 1 | a0001c0001t0001g0047 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.283+19872A>G | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 3/10 | chr11 | 43773993 | |||||||
| chr11:43774016 | T | C | 1 | a0001c0001t0001g0125 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.283+19895T>C | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 3/10 | chr11 | 43774016 | |||||||
| chr11:43774128 | C | T | 2 | a0001c0001t0001g0092 a0001c0001t0001g0094 |
2 | NA18952.hp1 NA19001.hp2 |
intron_variant | MODIFIER | c.283+20007C>T | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 3/10 | chr11 | 43774128 | |||||||
| chr11:43774218 | A | AT | 7 | a0001c0001t0001g0123 a0001c0001t0001g0125 a0001c0001t0001g0202 others(4): Show |
7 | HG01109.hp1 HG01884.hp2 HG02559.hp2 others(4): Show |
intron_variant | MODIFIER | c.283+20111dupT | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr11 | 43774218 | ||||||
| chr11:43774218 | AT | A | 5 | a0001c0001t0003g0206 a0001c0003t0003g0242 a0003c0004t0001g0241 others(2): Show |
5 | HG02647.hp2 HG03516.hp2 HG03579.hp1 others(2): Show |
intron_variant | MODIFIER | c.283+20111delT | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr11 | 43774218 | ||||||
| chr11:43774245 | C | T | 1 | a0001c0001t0001g0054 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.283+20124C>T | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 3/10 | chr11 | 43774245 | |||||||
| chr11:43774282 | C | T | 43 | a0001c0001t0001g0009 a0001c0001t0001g0128 a0001c0001t0001g0129 others(40): Show |
43 | HG00099.hp2 HG00140.hp1 HG00639.hp2 others(40): Show |
intron_variant | MODIFIER | c.283+20161C>T | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 3/10 | chr11 | 43774282 | |||||||
| chr11:43774389 | G | A | 1 | a0002c0002t0010g0157 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.283+20268G>A | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 3/10 | chr11 | 43774389 | |||||||
| chr11:43774465 | G | A | 16 | a0001c0001t0001g0002 a0001c0001t0001g0120 a0001c0001t0001g0121 others(13): Show |
17 | HG01109.hp1 HG01496.hp1 HG02258.hp2 others(14): Show |
intron_variant | MODIFIER | c.283+20344G>A | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 3/10 | chr11 | 43774465 | |||||||
| chr11:43774585 | T | C | 4 | a0001c0001t0003g0267 a0001c0001t0003g0268 a0001c0001t0003g0278 others(1): Show |
4 | HG02572.hp1 HG02965.hp2 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.283+20464T>C | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 3/10 | chr11 | 43774585 | |||||||
| chr11:43774633 | A | T | 1 | a0001c0001t0001g0065 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.283+20512A>T | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 3/10 | chr11 | 43774633 | |||||||
| chr11:43774862 | T | G | 21 | a0001c0001t0001g0002 a0001c0001t0001g0111 a0001c0001t0001g0112 others(18): Show |
22 | HG01109.hp1 HG01496.hp1 HG02055.hp1 others(19): Show |
intron_variant | MODIFIER | c.283+20741T>G | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 3/10 | chr11 | 43774862 | |||||||
| chr11:43775070 | T | C | 18 | a0001c0001t0001g0060 a0001c0001t0001g0061 a0001c0001t0001g0062 others(15): Show |
18 | HG00280.hp1 HG00609.hp2 HG02300.hp2 others(15): Show |
intron_variant | MODIFIER | c.283+20949T>C | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 3/10 | chr11 | 43775070 | |||||||
| chr11:43775087 | C | A | 5 | a0001c0001t0001g0111 a0001c0001t0001g0112 a0001c0001t0001g0202 others(2): Show |
5 | HG02055.hp1 HG02559.hp2 HG02809.hp2 others(2): Show |
intron_variant | MODIFIER | c.283+20966C>A | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 3/10 | chr11 | 43775087 | |||||||
| chr11:43775112 | G | A | 1 | a0002c0002t0008g0003 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.283+20991G>A | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 3/10 | chr11 | 43775112 | |||||||
| chr11:43775138 | C | T | 1 | a0001c0001t0001g0054 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.283+21017C>T | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 3/10 | chr11 | 43775138 | |||||||
| chr11:43775156 | C | T | 39 | a0001c0001t0001g0002 a0001c0001t0001g0060 a0001c0001t0001g0061 others(36): Show |
40 | HG00280.hp1 HG00609.hp2 HG01109.hp1 others(37): Show |
intron_variant | MODIFIER | c.283+21035C>T | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 3/10 | chr11 | 43775156 | |||||||
| chr11:43775184 | C | A | 14 | a0001c0001t0003g0013 a0001c0001t0003g0014 a0001c0001t0003g0015 others(11): Show |
14 | HG00280.hp1 HG00609.hp2 NA18612.hp2 others(11): Show |
intron_variant | MODIFIER | c.283+21063C>A | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 3/10 | chr11 | 43775184 | |||||||
| chr11:43775204 | G | A | 3 | a0001c0001t0001g0005 a0001c0001t0001g0007 a0001c0001t0001g0008 |
3 | HG02809.hp1 HG02886.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.283+21083G>A | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 3/10 | chr11 | 43775204 | |||||||
| chr11:43775249 | C | A | 18 | a0001c0001t0001g0060 a0001c0001t0001g0061 a0001c0001t0001g0062 others(15): Show |
18 | HG00280.hp1 HG00609.hp2 HG02300.hp2 others(15): Show |
intron_variant | MODIFIER | c.283+21128C>A | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 3/10 | chr11 | 43775249 | |||||||
| chr11:43775285 | C | CAT | 11 | a0002c0002t0002g0004 a0002c0002t0002g0138 a0002c0002t0002g0142 others(8): Show |
11 | HG01109.hp2 HG01884.hp1 HG02257.hp2 others(8): Show |
intron_variant | MODIFIER | c.283+21171_283+2117 others(6): Show |
HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr11 | 43775285 | ||||||
| chr11:43775318 | G | T | 21 | a0001c0001t0001g0002 a0001c0001t0001g0111 a0001c0001t0001g0112 others(18): Show |
22 | HG01109.hp1 HG01496.hp1 HG02055.hp1 others(19): Show |
intron_variant | MODIFIER | c.283+21197G>T | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 3/10 | chr11 | 43775318 | |||||||
| chr11:43775341 | A | G | 1 | a0002c0002t0008g0003 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.283+21220A>G | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 3/10 | chr11 | 43775341 | |||||||
| chr11:43775367 | T | C | 4 | a0001c0001t0001g0060 a0001c0001t0001g0061 a0001c0001t0001g0062 others(1): Show |
4 | HG02300.hp2 HG03453.hp2 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.283+21246T>C | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 3/10 | chr11 | 43775367 | |||||||
| chr11:43775484 | AT | A | 52 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(49): Show |
52 | HG00099.hp2 HG00140.hp1 HG00639.hp2 others(49): Show |
intron_variant | MODIFIER | c.283+21373delT | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr11 | 43775484 | ||||||
| chr11:43775714 | C | T | 14 | a0001c0001t0003g0013 a0001c0001t0003g0014 a0001c0001t0003g0015 others(11): Show |
14 | HG00280.hp1 HG00609.hp2 NA18612.hp2 others(11): Show |
intron_variant | MODIFIER | c.283+21593C>T | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 3/10 | chr11 | 43775714 | |||||||
| chr11:43775715 | G | A | 21 | a0001c0001t0001g0002 a0001c0001t0001g0111 a0001c0001t0001g0112 others(18): Show |
22 | HG01109.hp1 HG01496.hp1 HG02055.hp1 others(19): Show |
intron_variant | MODIFIER | c.283+21594G>A | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 3/10 | chr11 | 43775715 | |||||||
| chr11:43775742 | A | G | 3 | a0002c0002t0002g0187 a0002c0002t0002g0188 a0002c0002t0002g0189 |
3 | HG00140.hp2 HG01167.hp1 HG01346.hp1 |
intron_variant | MODIFIER | c.283+21621A>G | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 3/10 | chr11 | 43775742 | |||||||
| chr11:43775748 | T | C | 14 | a0001c0001t0003g0013 a0001c0001t0003g0014 a0001c0001t0003g0015 others(11): Show |
14 | HG00280.hp1 HG00609.hp2 NA18612.hp2 others(11): Show |
intron_variant | MODIFIER | c.283+21627T>C | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 3/10 | chr11 | 43775748 | |||||||
| chr11:43775758 | C | G | 14 | a0001c0001t0003g0013 a0001c0001t0003g0014 a0001c0001t0003g0015 others(11): Show |
14 | HG00280.hp1 HG00609.hp2 NA18612.hp2 others(11): Show |
intron_variant | MODIFIER | c.283+21637C>G | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 3/10 | chr11 | 43775758 | |||||||
| chr11:43775764 | C | T | 5 | a0001c0001t0001g0111 a0001c0001t0001g0112 a0001c0001t0001g0202 others(2): Show |
5 | HG02055.hp1 HG02559.hp2 HG02809.hp2 others(2): Show |
intron_variant | MODIFIER | c.283+21643C>T | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 3/10 | chr11 | 43775764 | |||||||
| chr11:43775817 | T | A | 4 | a0001c0001t0001g0060 a0001c0001t0001g0061 a0001c0001t0001g0062 others(1): Show |
4 | HG02300.hp2 HG03453.hp2 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.283+21696T>A | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 3/10 | chr11 | 43775817 | |||||||
| chr11:43775877 | C | A | 1 | a0002c0002t0002g0141 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.283+21756C>A | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 3/10 | chr11 | 43775877 | |||||||
| chr11:43775878 | A | G | 182 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(179): Show |
183 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(180): Show |
intron_variant | MODIFIER | c.283+21757A>G | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 3/10 | chr11 | 43775878 | |||||||
| chr11:43775924 | C | T | 66 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(63): Show |
66 | HG00099.hp2 HG00140.hp1 HG00609.hp2 others(63): Show |
intron_variant | MODIFIER | c.283+21803C>T | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 3/10 | chr11 | 43775924 | |||||||
| chr11:43776007 | G | A | 1 | a0001c0001t0001g0095 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.283+21886G>A | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 3/10 | chr11 | 43776007 | |||||||
| chr11:43776119 | A | C | 2 | a0001c0001t0001g0262 a0001c0001t0001g0263 |
2 | HG02258.hp2 HG02280.hp1 |
intron_variant | MODIFIER | c.283+21998A>C | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 3/10 | chr11 | 43776119 | |||||||
| chr11:43776291 | G | A | 14 | a0001c0001t0003g0013 a0001c0001t0003g0014 a0001c0001t0003g0015 others(11): Show |
14 | HG00280.hp1 HG00609.hp2 NA18612.hp2 others(11): Show |
intron_variant | MODIFIER | c.284-22029G>A | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 3/10 | chr11 | 43776291 | |||||||
| chr11:43776313 | G | T | 19 | a0001c0001t0001g0128 a0001c0001t0001g0129 a0001c0001t0001g0265 others(16): Show |
19 | HG00639.hp2 HG00642.hp2 HG01069.hp1 others(16): Show |
intron_variant | MODIFIER | c.284-22007G>T | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 3/10 | chr11 | 43776313 | |||||||
| chr11:43776337 | A | G | 18 | a0001c0001t0001g0060 a0001c0001t0001g0061 a0001c0001t0001g0062 others(15): Show |
18 | HG00280.hp1 HG00609.hp2 HG02300.hp2 others(15): Show |
intron_variant | MODIFIER | c.284-21983A>G | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 3/10 | chr11 | 43776337 | |||||||
| chr11:43776415 | G | A | 1 | a0001c0003t0003g0242 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.284-21905G>A | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 3/10 | chr11 | 43776415 | |||||||
| chr11:43776730 | C | T | 1 | a0002c0002t0002g0150 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.284-21590C>T | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 3/10 | chr11 | 43776730 | |||||||
| chr11:43776773 | G | A | 13 | a0001c0001t0003g0267 a0001c0001t0003g0268 a0001c0001t0003g0278 others(10): Show |
13 | HG01070.hp2 HG01071.hp1 HG02004.hp1 others(10): Show |
intron_variant | MODIFIER | c.284-21547G>A | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 3/10 | chr11 | 43776773 | |||||||
| chr11:43776802 | C | T | 2 | a0001c0003t0001g0238 a0001c0003t0001g0273 |
2 | HG00642.hp2 HG02735.hp2 |
intron_variant | MODIFIER | c.284-21518C>T | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 3/10 | chr11 | 43776802 | |||||||
| chr11:43776910 | A | G | 5 | a0002c0002t0002g0161 a0002c0002t0002g0175 a0002c0002t0002g0176 others(2): Show |
5 | HG02647.hp1 HG02723.hp1 HG03130.hp2 others(2): Show |
intron_variant | MODIFIER | c.284-21410A>G | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 3/10 | chr11 | 43776910 | |||||||
| chr11:43776924 | G | A | 1 | a0001c0001t0003g0206 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.284-21396G>A | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 3/10 | chr11 | 43776924 | |||||||
| chr11:43776941 | C | T | 7 | a0001c0003t0003g0242 a0001c0003t0003g0243 a0001c0003t0003g0244 others(4): Show |
7 | HG01070.hp2 HG01071.hp1 HG02004.hp1 others(4): Show |
intron_variant | MODIFIER | c.284-21379C>T | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 3/10 | chr11 | 43776941 | |||||||
| chr11:43776942 | T | A | 2 | a0002c0002t0004g0205 a0002c0002t0004g0274 |
2 | HG02451.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.284-21378T>A | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 3/10 | chr11 | 43776942 | |||||||
| chr11:43777010 | G | C | 14 | a0001c0001t0003g0013 a0001c0001t0003g0014 a0001c0001t0003g0015 others(11): Show |
14 | HG00280.hp1 HG00609.hp2 NA18612.hp2 others(11): Show |
intron_variant | MODIFIER | c.284-21310G>C | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 3/10 | chr11 | 43777010 | |||||||
| chr11:43777138 | T | C | 1 | a0001c0001t0001g0028 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.284-21182T>C | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 3/10 | chr11 | 43777138 | |||||||
| chr11:43777182 | T | G | 3 | a0001c0001t0001g0005 a0001c0001t0001g0007 a0001c0001t0001g0008 |
3 | HG02809.hp1 HG02886.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.284-21138T>G | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 3/10 | chr11 | 43777182 | |||||||
| chr11:43777183 | A | C | 3 | a0001c0001t0001g0005 a0001c0001t0001g0007 a0001c0001t0001g0008 |
3 | HG02809.hp1 HG02886.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.284-21137A>C | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 3/10 | chr11 | 43777183 | |||||||
| chr11:43777185 | AT | A | 3 | a0001c0001t0001g0005 a0001c0001t0001g0007 a0001c0001t0001g0008 |
3 | HG02809.hp1 HG02886.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.284-21133delT | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr11 | 43777185 | ||||||
| chr11:43777190 | C | CAAGGCAA | 3 | a0001c0001t0001g0005 a0001c0001t0001g0007 a0001c0001t0001g0008 |
3 | HG02809.hp1 HG02886.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.284-21130_284-2112 others(11): Show |
HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 3/10 | chr11 | 43777190 | |||||||
| chr11:43777280 | G | C | 14 | a0001c0001t0003g0013 a0001c0001t0003g0014 a0001c0001t0003g0015 others(11): Show |
14 | HG00280.hp1 HG00609.hp2 NA18612.hp2 others(11): Show |
intron_variant | MODIFIER | c.284-21040G>C | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 3/10 | chr11 | 43777280 | |||||||
| chr11:43777322 | A | G | 2 | a0001c0003t0001g0238 a0001c0003t0001g0273 |
2 | HG00642.hp2 HG02735.hp2 |
intron_variant | MODIFIER | c.284-20998A>G | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 3/10 | chr11 | 43777322 | |||||||
| chr11:43777506 | G | T | 1 | a0002c0002t0002g0116 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.284-20814G>T | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 3/10 | chr11 | 43777506 | |||||||
| chr11:43777553 | C | G | 4 | a0001c0001t0001g0060 a0001c0001t0001g0061 a0001c0001t0001g0062 others(1): Show |
4 | HG02300.hp2 HG03453.hp2 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.284-20767C>G | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 3/10 | chr11 | 43777553 | |||||||
| chr11:43777573 | G | C | 2 | a0001c0003t0001g0197 a0001c0003t0001g0198 |
2 | HG03669.hp2 HG04199.hp2 |
intron_variant | MODIFIER | c.284-20747G>C | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 3/10 | chr11 | 43777573 | |||||||
| chr11:43777576 | C | T | 182 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(179): Show |
183 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(180): Show |
intron_variant | MODIFIER | c.284-20744C>T | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 3/10 | chr11 | 43777576 | |||||||
| chr11:43777684 | C | T | 4 | a0001c0001t0003g0267 a0001c0001t0003g0268 a0001c0001t0003g0278 others(1): Show |
4 | HG02572.hp1 HG02965.hp2 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.284-20636C>T | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 3/10 | chr11 | 43777684 | |||||||
| chr11:43777725 | A | G | 16 | a0001c0001t0001g0002 a0001c0001t0001g0120 a0001c0001t0001g0121 others(13): Show |
17 | HG01109.hp1 HG01496.hp1 HG02258.hp2 others(14): Show |
intron_variant | MODIFIER | c.284-20595A>G | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 3/10 | chr11 | 43777725 | |||||||
| chr11:43777748 | G | A | 27 | a0001c0001t0003g0013 a0001c0001t0003g0014 a0001c0001t0003g0015 others(24): Show |
27 | HG00280.hp1 HG00609.hp2 HG01070.hp2 others(24): Show |
intron_variant | MODIFIER | c.284-20572G>A | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 3/10 | chr11 | 43777748 | |||||||
| chr11:43777825 | T | A | 1 | a0002c0002t0010g0157 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.284-20495T>A | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 3/10 | chr11 | 43777825 | |||||||
| chr11:43777825 | T | C | 14 | a0001c0001t0003g0013 a0001c0001t0003g0014 a0001c0001t0003g0015 others(11): Show |
14 | HG00280.hp1 HG00609.hp2 NA18612.hp2 others(11): Show |
intron_variant | MODIFIER | c.284-20495T>C | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 3/10 | chr11 | 43777825 | |||||||
| chr11:43777895 | T | C | 2 | a0001c0001t0001g0262 a0001c0001t0001g0263 |
2 | HG02258.hp2 HG02280.hp1 |
intron_variant | MODIFIER | c.284-20425T>C | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 3/10 | chr11 | 43777895 | |||||||
| chr11:43777905 | G | A | 14 | a0001c0001t0003g0013 a0001c0001t0003g0014 a0001c0001t0003g0015 others(11): Show |
14 | HG00280.hp1 HG00609.hp2 NA18612.hp2 others(11): Show |
intron_variant | MODIFIER | c.284-20415G>A | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 3/10 | chr11 | 43777905 | |||||||
| chr11:43777929 | A | G | 1 | a0002c0002t0002g0275 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.284-20391A>G | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 3/10 | chr11 | 43777929 | |||||||
| chr11:43777964 | G | A | 9 | a0001c0001t0001g0002 a0001c0001t0001g0120 a0001c0001t0001g0121 others(6): Show |
10 | HG01109.hp1 HG01496.hp1 HG02258.hp2 others(7): Show |
intron_variant | MODIFIER | c.284-20356G>A | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 3/10 | chr11 | 43777964 | |||||||
| chr11:43778153 | A | G | 1 | a0001c0001t0001g0256 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.284-20167A>G | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 3/10 | chr11 | 43778153 | |||||||
| chr11:43778204 | C | G | 1 | a0001c0001t0001g0254 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.284-20116C>G | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 3/10 | chr11 | 43778204 | |||||||
| chr11:43778211 | A | G | 16 | a0001c0001t0001g0002 a0001c0001t0001g0120 a0001c0001t0001g0121 others(13): Show |
17 | HG01109.hp1 HG01496.hp1 HG02258.hp2 others(14): Show |
intron_variant | MODIFIER | c.284-20109A>G | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 3/10 | chr11 | 43778211 | |||||||
| chr11:43778219 | A | T | 1 | a0001c0001t0001g0065 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.284-20101A>T | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 3/10 | chr11 | 43778219 | |||||||
| chr11:43778287 | A | C | 1 | a0002c0002t0008g0003 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.284-20033A>C | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 3/10 | chr11 | 43778287 | |||||||
| chr11:43778321 | T | G | 1 | a0002c0002t0002g0155 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.284-19999T>G | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 3/10 | chr11 | 43778321 | |||||||
| chr11:43778429 | C | T | 14 | a0001c0001t0003g0013 a0001c0001t0003g0014 a0001c0001t0003g0015 others(11): Show |
14 | HG00280.hp1 HG00609.hp2 NA18612.hp2 others(11): Show |
intron_variant | MODIFIER | c.284-19891C>T | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 3/10 | chr11 | 43778429 | |||||||
| chr11:43778514 | C | T | 21 | a0001c0001t0001g0002 a0001c0001t0001g0111 a0001c0001t0001g0112 others(18): Show |
22 | HG01109.hp1 HG01496.hp1 HG02055.hp1 others(19): Show |
intron_variant | MODIFIER | c.284-19806C>T | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 3/10 | chr11 | 43778514 | |||||||
| chr11:43778586 | A | G | 15 | a0001c0001t0003g0013 a0001c0001t0003g0014 a0001c0001t0003g0015 others(12): Show |
15 | HG00280.hp1 HG00609.hp2 NA18612.hp2 others(12): Show |
intron_variant | MODIFIER | c.284-19734A>G | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 3/10 | chr11 | 43778586 | |||||||
| chr11:43778924 | A | G | 94 | a0001c0001t0001g0026 a0001c0001t0001g0028 a0001c0001t0001g0029 others(91): Show |
94 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(91): Show |
intron_variant | MODIFIER | c.284-19396A>G | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 3/10 | chr11 | 43778924 | |||||||
| chr11:43778985 | T | G | 2 | a0002c0002t0002g0039 a0002c0002t0002g0158 |
2 | HG02683.hp1 HG02698.hp1 |
intron_variant | MODIFIER | c.284-19335T>G | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 3/10 | chr11 | 43778985 | |||||||
| chr11:43779076 | T | G | 93 | a0001c0001t0001g0002 a0001c0001t0001g0026 a0001c0001t0001g0028 others(90): Show |
94 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(91): Show |
intron_variant | MODIFIER | c.284-19244T>G | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 3/10 | chr11 | 43779076 | |||||||
| chr11:43779118 | A | G | 14 | a0001c0001t0003g0013 a0001c0001t0003g0014 a0001c0001t0003g0015 others(11): Show |
14 | HG00280.hp1 HG00609.hp2 NA18612.hp2 others(11): Show |
intron_variant | MODIFIER | c.284-19202A>G | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 3/10 | chr11 | 43779118 | |||||||
| chr11:43779139 | G | T | 53 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(50): Show |
53 | HG00099.hp2 HG00140.hp1 HG00639.hp2 others(50): Show |
intron_variant | MODIFIER | c.284-19181G>T | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 3/10 | chr11 | 43779139 | |||||||
| chr11:43779141 | A | T | 1 | a0001c0001t0003g0206 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.284-19179A>T | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 3/10 | chr11 | 43779141 | |||||||
| chr11:43779154 | C | T | 1 | a0001c0001t0003g0206 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.284-19166C>T | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 3/10 | chr11 | 43779154 | |||||||
| chr11:43779217 | G | A | 1 | a0002c0002t0008g0003 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.284-19103G>A | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 3/10 | chr11 | 43779217 | |||||||
| chr11:43779218 | A | G | 1 | a0002c0002t0008g0003 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.284-19102A>G | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 3/10 | chr11 | 43779218 | |||||||
| chr11:43779457 | A | G | 1 | a0002c0002t0002g0151 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.284-18863A>G | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 3/10 | chr11 | 43779457 | |||||||
| chr11:43779511 | A | T | 18 | a0001c0001t0001g0060 a0001c0001t0001g0061 a0001c0001t0001g0062 others(15): Show |
18 | HG00280.hp1 HG00609.hp2 HG02300.hp2 others(15): Show |
intron_variant | MODIFIER | c.284-18809A>T | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 3/10 | chr11 | 43779511 | |||||||
| chr11:43779519 | G | T | 1 | a0002c0002t0009g0200 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.284-18801G>T | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 3/10 | chr11 | 43779519 | |||||||
| chr11:43779552 | C | A | 1 | a0002c0002t0002g0138 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.284-18768C>A | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 3/10 | chr11 | 43779552 | |||||||
| chr11:43779582 | A | G | 1 | a0001c0001t0001g0087 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.284-18738A>G | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 3/10 | chr11 | 43779582 | |||||||
| chr11:43779728 | A | G | 1 | a0001c0001t0001g0097 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.284-18592A>G | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 3/10 | chr11 | 43779728 | |||||||
| chr11:43779803 | C | A | 1 | a0002c0002t0008g0003 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.284-18517C>A | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 3/10 | chr11 | 43779803 | |||||||
| chr11:43779845 | A | G | 1 | a0001c0001t0001g0213 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.284-18475A>G | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 3/10 | chr11 | 43779845 | |||||||
| chr11:43779947 | A | G | 2 | a0001c0003t0001g0197 a0001c0003t0001g0198 |
2 | HG03669.hp2 HG04199.hp2 |
intron_variant | MODIFIER | c.284-18373A>G | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 3/10 | chr11 | 43779947 | |||||||
| chr11:43779966 | GGTAATCC others(1): Show |
G | 14 | a0001c0001t0003g0013 a0001c0001t0003g0014 a0001c0001t0003g0015 others(11): Show |
14 | HG00280.hp1 HG00609.hp2 NA18612.hp2 others(11): Show |
intron_variant | MODIFIER | c.284-18351_284-1834 others(12): Show |
HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr11 | 43779966 | ||||||
| chr11:43780082 | C | G | 4 | a0001c0001t0001g0060 a0001c0001t0001g0061 a0001c0001t0001g0062 others(1): Show |
4 | HG02300.hp2 HG03453.hp2 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.284-18238C>G | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 3/10 | chr11 | 43780082 | |||||||
| chr11:43780245 | A | C | 1 | a0002c0002t0002g0116 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.284-18075A>C | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 3/10 | chr11 | 43780245 | |||||||
| chr11:43780275 | C | T | 21 | a0001c0001t0001g0002 a0001c0001t0001g0111 a0001c0001t0001g0112 others(18): Show |
22 | HG01109.hp1 HG01496.hp1 HG02055.hp1 others(19): Show |
intron_variant | MODIFIER | c.284-18045C>T | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 3/10 | chr11 | 43780275 | |||||||
| chr11:43781160 | A | G | 1 | a0001c0001t0001g0054 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.284-17160A>G | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 3/10 | chr11 | 43781160 | |||||||
| chr11:43781316 | C | A | 13 | a0001c0001t0003g0013 a0001c0001t0003g0014 a0001c0001t0003g0015 others(10): Show |
13 | HG00609.hp2 NA18612.hp2 NA18747.hp1 others(10): Show |
intron_variant | MODIFIER | c.284-17004C>A | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 3/10 | chr11 | 43781316 | |||||||
| chr11:43781364 | T | TG | 14 | a0001c0001t0003g0013 a0001c0001t0003g0014 a0001c0001t0003g0015 others(11): Show |
14 | HG00280.hp1 HG00609.hp2 NA18612.hp2 others(11): Show |
intron_variant | MODIFIER | c.284-16955dupG | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr11 | 43781364 | ||||||
| chr11:43781414 | T | C | 1 | a0001c0003t0001g0239 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.284-16906T>C | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 3/10 | chr11 | 43781414 | |||||||
| chr11:43781563 | A | G | 72 | a0001c0001t0001g0026 a0001c0001t0001g0028 a0001c0001t0001g0029 others(69): Show |
72 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(69): Show |
intron_variant | MODIFIER | c.284-16757A>G | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 3/10 | chr11 | 43781563 | |||||||
| chr11:43781608 | T | C | 14 | a0001c0001t0003g0013 a0001c0001t0003g0014 a0001c0001t0003g0015 others(11): Show |
14 | HG00280.hp1 HG00609.hp2 NA18612.hp2 others(11): Show |
intron_variant | MODIFIER | c.284-16712T>C | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 3/10 | chr11 | 43781608 | |||||||
| chr11:43781646 | A | T | 14 | a0001c0001t0003g0013 a0001c0001t0003g0014 a0001c0001t0003g0015 others(11): Show |
14 | HG00280.hp1 HG00609.hp2 NA18612.hp2 others(11): Show |
intron_variant | MODIFIER | c.284-16674A>T | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 3/10 | chr11 | 43781646 | |||||||
| chr11:43781704 | G | A | 182 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(179): Show |
183 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(180): Show |
intron_variant | MODIFIER | c.284-16616G>A | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 3/10 | chr11 | 43781704 | |||||||
| chr11:43781780 | TTAAC | T | 2 | a0001c0003t0003g0231 a0001c0003t0003g0232 |
2 | HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.284-16536_284-1653 others(8): Show |
HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr11 | 43781780 | ||||||
| chr11:43782007 | G | A | 1 | a0002c0002t0008g0003 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.284-16313G>A | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 3/10 | chr11 | 43782007 | |||||||
| chr11:43782308 | G | A | 1 | a0002c0002t0002g0166 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.284-16012G>A | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 3/10 | chr11 | 43782308 | |||||||
| chr11:43782403 | G | A | 1 | a0001c0001t0001g0088 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.284-15917G>A | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 3/10 | chr11 | 43782403 | |||||||
| chr11:43782509 | C | T | 1 | a0001c0001t0003g0015 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.284-15811C>T | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 3/10 | chr11 | 43782509 | |||||||
| chr11:43782599 | C | T | 1 | a0001c0003t0001g0237 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.284-15721C>T | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 3/10 | chr11 | 43782599 | |||||||
| chr11:43782669 | T | C | 18 | a0001c0001t0001g0060 a0001c0001t0001g0061 a0001c0001t0001g0062 others(15): Show |
18 | HG00280.hp1 HG00609.hp2 HG02300.hp2 others(15): Show |
intron_variant | MODIFIER | c.284-15651T>C | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 3/10 | chr11 | 43782669 | |||||||
| chr11:43782674 | C | CA | 65 | a0001c0001t0001g0026 a0001c0001t0001g0028 a0001c0001t0001g0029 others(62): Show |
65 | HG00408.hp1 HG00423.hp2 HG00735.hp2 others(62): Show |
intron_variant | MODIFIER | c.284-15630dupA | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr11 | 43782674 | ||||||
| chr11:43782674 | CA | C | 18 | a0001c0001t0003g0013 a0001c0001t0003g0014 a0001c0001t0003g0015 others(15): Show |
18 | HG00280.hp1 HG00609.hp2 HG02451.hp1 others(15): Show |
intron_variant | MODIFIER | c.284-15630delA | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr11 | 43782674 | ||||||
| chr11:43782702 | G | A | 1 | a0002c0002t0002g0110 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.284-15618G>A | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 3/10 | chr11 | 43782702 | |||||||
| chr11:43782769 | A | G | 1 | a0002c0002t0002g0187 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.284-15551A>G | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 3/10 | chr11 | 43782769 | |||||||
| chr11:43782876 | A | G | 1 | a0002c0002t0004g0205 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.284-15444A>G | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 3/10 | chr11 | 43782876 | |||||||
| chr11:43782880 | G | A | 10 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(7): Show |
10 | HG01884.hp2 HG02257.hp1 HG02717.hp2 others(7): Show |
intron_variant | MODIFIER | c.284-15440G>A | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 3/10 | chr11 | 43782880 | |||||||
| chr11:43783030 | A | G | 7 | a0001c0003t0003g0242 a0001c0003t0003g0243 a0001c0003t0003g0244 others(4): Show |
7 | HG01070.hp2 HG01071.hp1 HG02004.hp1 others(4): Show |
intron_variant | MODIFIER | c.284-15290A>G | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 3/10 | chr11 | 43783030 | |||||||
| chr11:43783130 | A | G | 13 | a0001c0001t0003g0267 a0001c0001t0003g0268 a0001c0001t0003g0278 others(10): Show |
13 | HG01070.hp2 HG01071.hp1 HG02004.hp1 others(10): Show |
intron_variant | MODIFIER | c.284-15190A>G | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 3/10 | chr11 | 43783130 | |||||||
| chr11:43783331 | G | A | 13 | a0001c0001t0003g0267 a0001c0001t0003g0268 a0001c0001t0003g0278 others(10): Show |
13 | HG01070.hp2 HG01071.hp1 HG02004.hp1 others(10): Show |
intron_variant | MODIFIER | c.284-14989G>A | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 3/10 | chr11 | 43783331 | |||||||
| chr11:43783397 | C | CT | 15 | a0001c0001t0001g0009 a0001c0001t0001g0060 a0001c0001t0001g0061 others(12): Show |
15 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(12): Show |
intron_variant | MODIFIER | c.284-14908dupT | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr11 | 43783397 | ||||||
| chr11:43783604 | C | G | 19 | a0001c0001t0001g0128 a0001c0001t0001g0129 a0001c0001t0001g0265 others(16): Show |
19 | HG00639.hp2 HG00642.hp2 HG01069.hp1 others(16): Show |
intron_variant | MODIFIER | c.284-14716C>G | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 3/10 | chr11 | 43783604 | |||||||
| chr11:43783614 | TC | T | 13 | a0001c0001t0003g0013 a0001c0001t0003g0014 a0001c0001t0003g0015 others(10): Show |
13 | HG00609.hp2 NA18612.hp2 NA18747.hp1 others(10): Show |
intron_variant | MODIFIER | c.284-14704delC | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr11 | 43783614 | ||||||
| chr11:43783666 | C | T | 1 | a0001c0001t0001g0047 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.284-14654C>T | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 3/10 | chr11 | 43783666 | |||||||
| chr11:43783797 | T | TA | 23 | a0001c0001t0001g0009 a0001c0001t0001g0186 a0001c0001t0001g0208 others(20): Show |
23 | HG00099.hp2 HG00140.hp1 HG01167.hp2 others(20): Show |
intron_variant | MODIFIER | c.284-14522dupA | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr11 | 43783797 | ||||||
| chr11:43783955 | C | G | 93 | a0001c0001t0001g0002 a0001c0001t0001g0026 a0001c0001t0001g0028 others(90): Show |
94 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(91): Show |
intron_variant | MODIFIER | c.284-14365C>G | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 3/10 | chr11 | 43783955 | |||||||
| chr11:43784301 | A | ATAT | 20 | a0001c0001t0001g0113 a0001c0001t0001g0259 a0001c0001t0001g0260 others(17): Show |
20 | HG00408.hp2 HG01099.hp2 HG01106.hp2 others(17): Show |
intron_variant | MODIFIER | c.284-13975_284-1397 others(7): Show |
HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr11 | 43784301 | ||||||
| chr11:43784301 | A | ATATTAT | 3 | a0002c0002t0002g0153 a0002c0002t0002g0156 a0002c0002t0002g0177 |
3 | HG02630.hp2 HG02717.hp1 HG02723.hp1 |
intron_variant | MODIFIER | c.284-13978_284-1397 others(10): Show |
HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr11 | 43784301 | ||||||
| chr11:43784301 | ATAT | A | 46 | a0001c0001t0001g0009 a0001c0001t0001g0028 a0001c0001t0001g0040 others(43): Show |
46 | HG00099.hp2 HG00140.hp1 HG00423.hp1 others(43): Show |
intron_variant | MODIFIER | c.284-13975_284-1397 others(7): Show |
HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr11 | 43784301 | ||||||
| chr11:43784301 | ATATTAT | A | 84 | a0001c0001t0001g0005 a0001c0001t0001g0007 a0001c0001t0001g0008 others(81): Show |
84 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(81): Show |
intron_variant | MODIFIER | c.284-13978_284-1397 others(10): Show |
HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr11 | 43784301 | ||||||
| chr11:43784301 | ATATTATT others(2): Show |
A | 6 | a0001c0001t0001g0006 a0001c0001t0001g0010 a0001c0001t0001g0032 others(3): Show |
6 | HG01884.hp2 HG02257.hp1 HG02717.hp2 others(3): Show |
intron_variant | MODIFIER | c.284-13981_284-1397 others(13): Show |
HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr11 | 43784301 | ||||||
| chr11:43784301 | ATATTATT others(5): Show |
A | 1 | a0002c0002t0002g0117 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.284-13984_284-1397 others(16): Show |
HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr11 | 43784301 | ||||||
| chr11:43784301 | ATATTATT others(11): Show |
A | 1 | a0001c0001t0001g0223 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.284-13990_284-1397 others(22): Show |
HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr11 | 43784301 | ||||||
| chr11:43784432 | T | A | 21 | a0002c0002t0002g0027 a0002c0002t0002g0109 a0002c0002t0002g0116 others(18): Show |
21 | HG00280.hp2 HG00423.hp1 HG00738.hp1 others(18): Show |
intron_variant | MODIFIER | c.284-13888T>A | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 3/10 | chr11 | 43784432 | |||||||
| chr11:43784433 | C | A | 21 | a0002c0002t0002g0027 a0002c0002t0002g0109 a0002c0002t0002g0116 others(18): Show |
21 | HG00280.hp2 HG00423.hp1 HG00738.hp1 others(18): Show |
intron_variant | MODIFIER | c.284-13887C>A | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 3/10 | chr11 | 43784433 | |||||||
| chr11:43784726 | G | T | 2 | a0001c0001t0001g0070 a0001c0001t0001g0095 |
2 | HG03239.hp1 HG03669.hp1 |
intron_variant | MODIFIER | c.284-13594G>T | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 3/10 | chr11 | 43784726 | |||||||
| chr11:43784828 | C | A | 2 | a0002c0002t0002g0039 a0002c0002t0002g0158 |
2 | HG02683.hp1 HG02698.hp1 |
intron_variant | MODIFIER | c.284-13492C>A | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 3/10 | chr11 | 43784828 | |||||||
| chr11:43784898 | A | G | 1 | a0001c0001t0001g0271 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.284-13422A>G | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 3/10 | chr11 | 43784898 | |||||||
| chr11:43785096 | GT | G | 169 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(166): Show |
170 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(167): Show |
intron_variant | MODIFIER | c.284-13213delT | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr11 | 43785096 | ||||||
| chr11:43785097 | T | G | 1 | a0002c0002t0002g0155 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.284-13223T>G | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 3/10 | chr11 | 43785097 | |||||||
| chr11:43785187 | G | A | 21 | a0001c0001t0001g0186 a0001c0001t0001g0208 a0001c0001t0001g0209 others(18): Show |
21 | HG00099.hp2 HG00140.hp1 HG01167.hp2 others(18): Show |
intron_variant | MODIFIER | c.284-13133G>A | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 3/10 | chr11 | 43785187 | |||||||
| chr11:43785357 | G | A | 14 | a0001c0001t0003g0013 a0001c0001t0003g0014 a0001c0001t0003g0015 others(11): Show |
14 | HG00280.hp1 HG00609.hp2 NA18612.hp2 others(11): Show |
intron_variant | MODIFIER | c.284-12963G>A | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 3/10 | chr11 | 43785357 | |||||||
| chr11:43785407 | A | G | 2 | a0002c0002t0004g0205 a0002c0002t0004g0274 |
2 | HG02451.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.284-12913A>G | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 3/10 | chr11 | 43785407 | |||||||
| chr11:43785452 | G | A | 53 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(50): Show |
53 | HG00099.hp2 HG00140.hp1 HG00639.hp2 others(50): Show |
intron_variant | MODIFIER | c.284-12868G>A | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 3/10 | chr11 | 43785452 | |||||||
| chr11:43785475 | C | T | 4 | a0002c0002t0002g0165 a0002c0002t0002g0180 a0004c0005t0002g0011 others(1): Show |
4 | HG00323.hp1 HG01099.hp2 HG01106.hp2 others(1): Show |
intron_variant | MODIFIER | c.284-12845C>T | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 3/10 | chr11 | 43785475 | |||||||
| chr11:43785723 | T | C | 17 | a0001c0001t0003g0267 a0001c0001t0003g0268 a0001c0001t0003g0278 others(14): Show |
17 | HG01070.hp2 HG01071.hp1 HG02004.hp1 others(14): Show |
intron_variant | MODIFIER | c.284-12597T>C | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 3/10 | chr11 | 43785723 | |||||||
| chr11:43785752 | T | C | 1 | a0002c0002t0002g0163 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.284-12568T>C | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 3/10 | chr11 | 43785752 | |||||||
| chr11:43785842 | T | G | 54 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(51): Show |
54 | HG00099.hp2 HG00140.hp1 HG00639.hp2 others(51): Show |
intron_variant | MODIFIER | c.284-12478T>G | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 3/10 | chr11 | 43785842 | |||||||
| chr11:43785971 | A | G | 19 | a0001c0001t0001g0128 a0001c0001t0001g0129 a0001c0001t0001g0265 others(16): Show |
19 | HG00639.hp2 HG00642.hp2 HG01069.hp1 others(16): Show |
intron_variant | MODIFIER | c.284-12349A>G | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 3/10 | chr11 | 43785971 | |||||||
| chr11:43786168 | G | A | 9 | a0002c0002t0002g0004 a0002c0002t0002g0144 a0002c0002t0002g0145 others(6): Show |
9 | HG00609.hp1 HG01884.hp1 HG02622.hp1 others(6): Show |
intron_variant | MODIFIER | c.284-12152G>A | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 3/10 | chr11 | 43786168 | |||||||
| chr11:43786292 | A | T | 14 | a0001c0001t0003g0013 a0001c0001t0003g0014 a0001c0001t0003g0015 others(11): Show |
14 | HG00280.hp1 HG00609.hp2 NA18612.hp2 others(11): Show |
intron_variant | MODIFIER | c.284-12028A>T | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 3/10 | chr11 | 43786292 | |||||||
| chr11:43786423 | A | G | 1 | a0001c0001t0001g0050 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.284-11897A>G | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 3/10 | chr11 | 43786423 | |||||||
| chr11:43786441 | T | C | 93 | a0001c0001t0001g0002 a0001c0001t0001g0026 a0001c0001t0001g0028 others(90): Show |
94 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(91): Show |
intron_variant | MODIFIER | c.284-11879T>C | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 3/10 | chr11 | 43786441 | |||||||
| chr11:43786683 | A | G | 4 | a0002c0002t0002g0001 a0002c0002t0002g0025 a0002c0002t0002g0038 others(1): Show |
5 | HG00642.hp1 HG01069.hp2 HG01071.hp2 others(2): Show |
intron_variant | MODIFIER | c.284-11637A>G | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 3/10 | chr11 | 43786683 | |||||||
| chr11:43786701 | A | G | 14 | a0001c0001t0003g0013 a0001c0001t0003g0014 a0001c0001t0003g0015 others(11): Show |
14 | HG00280.hp1 HG00609.hp2 NA18612.hp2 others(11): Show |
intron_variant | MODIFIER | c.284-11619A>G | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 3/10 | chr11 | 43786701 | |||||||
| chr11:43786724 | T | C | 33 | a0002c0002t0002g0001 a0002c0002t0002g0025 a0002c0002t0002g0037 others(30): Show |
34 | HG00140.hp2 HG00323.hp1 HG00639.hp1 others(31): Show |
intron_variant | MODIFIER | c.284-11596T>C | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 3/10 | chr11 | 43786724 | |||||||
| chr11:43786926 | G | A | 1 | a0001c0003t0001g0273 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.284-11394G>A | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 3/10 | chr11 | 43786926 | |||||||
| chr11:43786954 | T | C | 1 | a0001c0001t0001g0074 | 1 | NA19085.hp2 | intron_variant | MODIFIER | c.284-11366T>C | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 3/10 | chr11 | 43786954 | |||||||
| chr11:43787013 | C | T | 3 | a0002c0002t0002g0192 a0002c0002t0002g0193 a0002c0002t0002g0194 |
3 | HG02559.hp1 HG03516.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.284-11307C>T | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 3/10 | chr11 | 43787013 | |||||||
| chr11:43787322 | A | G | 2 | a0001c0003t0001g0197 a0001c0003t0001g0198 |
2 | HG03669.hp2 HG04199.hp2 |
intron_variant | MODIFIER | c.284-10998A>G | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 3/10 | chr11 | 43787322 | |||||||
| chr11:43787361 | G | T | 1 | a0002c0002t0008g0003 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.284-10959G>T | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 3/10 | chr11 | 43787361 | |||||||
| chr11:43787489 | C | T | 14 | a0001c0001t0003g0013 a0001c0001t0003g0014 a0001c0001t0003g0015 others(11): Show |
14 | HG00280.hp1 HG00609.hp2 NA18612.hp2 others(11): Show |
intron_variant | MODIFIER | c.284-10831C>T | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 3/10 | chr11 | 43787489 | |||||||
| chr11:43787502 | C | T | 4 | a0001c0001t0003g0267 a0001c0001t0003g0268 a0001c0001t0003g0278 others(1): Show |
4 | HG02572.hp1 HG02965.hp2 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.284-10818C>T | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 3/10 | chr11 | 43787502 | |||||||
| chr11:43787736 | C | T | 1 | a0001c0001t0001g0053 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.284-10584C>T | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 3/10 | chr11 | 43787736 | |||||||
| chr11:43787738 | G | GA | 91 | a0001c0001t0001g0002 a0001c0001t0001g0026 a0001c0001t0001g0028 others(88): Show |
92 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(89): Show |
intron_variant | MODIFIER | c.284-10569dupA | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr11 | 43787738 | ||||||
| chr11:43787746 | A | T | 4 | a0001c0001t0001g0060 a0001c0001t0001g0061 a0001c0001t0001g0062 others(1): Show |
4 | HG02300.hp2 HG03453.hp2 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.284-10574A>T | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 3/10 | chr11 | 43787746 | |||||||
| chr11:43787749 | A | T | 28 | a0001c0001t0001g0060 a0001c0001t0001g0061 a0001c0001t0001g0062 others(25): Show |
28 | HG00280.hp1 HG00609.hp2 HG00642.hp2 others(25): Show |
intron_variant | MODIFIER | c.284-10571A>T | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 3/10 | chr11 | 43787749 | |||||||
| chr11:43787752 | T | A | 11 | a0001c0001t0001g0044 a0001c0001t0001g0051 a0001c0001t0001g0052 others(8): Show |
11 | HG00639.hp1 HG01070.hp1 HG01192.hp1 others(8): Show |
intron_variant | MODIFIER | c.284-10568T>A | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 3/10 | chr11 | 43787752 | |||||||
| chr11:43787857 | C | T | 4 | a0001c0001t0001g0060 a0001c0001t0001g0061 a0001c0001t0001g0062 others(1): Show |
4 | HG02300.hp2 HG03453.hp2 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.284-10463C>T | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 3/10 | chr11 | 43787857 | |||||||
| chr11:43788045 | A | T | 1 | a0002c0002t0008g0003 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.284-10275A>T | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 3/10 | chr11 | 43788045 | |||||||
| chr11:43788136 | CTT | C | 17 | a0001c0001t0003g0267 a0001c0001t0003g0268 a0001c0001t0003g0278 others(14): Show |
17 | HG01070.hp2 HG01071.hp1 HG02004.hp1 others(14): Show |
intron_variant | MODIFIER | c.284-10180_284-1017 others(6): Show |
HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr11 | 43788136 | ||||||
| chr11:43788283 | C | T | 52 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(49): Show |
52 | HG00099.hp2 HG00140.hp1 HG00639.hp2 others(49): Show |
intron_variant | MODIFIER | c.284-10037C>T | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 3/10 | chr11 | 43788283 | |||||||
| chr11:43788445 | C | T | 1 | a0001c0001t0001g0271 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.284-9875C>T | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 3/10 | chr11 | 43788445 | |||||||
| chr11:43788554 | C | T | 4 | a0001c0001t0001g0060 a0001c0001t0001g0061 a0001c0001t0001g0062 others(1): Show |
4 | HG02300.hp2 HG03453.hp2 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.284-9766C>T | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 3/10 | chr11 | 43788554 | |||||||
| chr11:43788612 | T | C | 1 | a0001c0001t0001g0089 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.284-9708T>C | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 3/10 | chr11 | 43788612 | |||||||
| chr11:43788639 | A | G | 1 | a0002c0002t0002g0141 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.284-9681A>G | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 3/10 | chr11 | 43788639 | |||||||
| chr11:43788685 | CA | C | 32 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(29): Show |
32 | HG00099.hp2 HG00140.hp1 HG01167.hp2 others(29): Show |
intron_variant | MODIFIER | c.284-9611delA | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr11 | 43788685 | ||||||
| chr11:43788685 | CAAAAA | C | 84 | a0001c0001t0001g0002 a0001c0001t0001g0026 a0001c0001t0001g0028 others(81): Show |
85 | HG00099.hp1 HG00408.hp1 HG00423.hp2 others(82): Show |
intron_variant | MODIFIER | c.284-9615_284-9611d others(7): Show |
HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr11 | 43788685 | ||||||
| chr11:43788685 | CAAAAAAA | C | 14 | a0001c0001t0003g0013 a0001c0001t0003g0014 a0001c0001t0003g0015 others(11): Show |
14 | HG00280.hp1 HG00609.hp2 NA18612.hp2 others(11): Show |
intron_variant | MODIFIER | c.284-9617_284-9611d others(9): Show |
HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr11 | 43788685 | ||||||
| chr11:43788709 | A | C | 3 | a0001c0001t0001g0060 a0001c0001t0001g0062 a0001c0001t0001g0113 |
3 | HG02300.hp2 HG03453.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.284-9611A>C | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 3/10 | chr11 | 43788709 | |||||||
| chr11:43788794 | A | T | 1 | a0001c0003t0001g0229 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.284-9526A>T | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 3/10 | chr11 | 43788794 | |||||||
| chr11:43788909 | T | C | 111 | a0001c0001t0001g0002 a0001c0001t0001g0026 a0001c0001t0001g0028 others(108): Show |
112 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(109): Show |
intron_variant | MODIFIER | c.284-9411T>C | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 3/10 | chr11 | 43788909 | |||||||
| chr11:43788949 | A | G | 16 | a0001c0001t0001g0002 a0001c0001t0001g0120 a0001c0001t0001g0121 others(13): Show |
17 | HG01109.hp1 HG01496.hp1 HG02258.hp2 others(14): Show |
intron_variant | MODIFIER | c.284-9371A>G | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 3/10 | chr11 | 43788949 | |||||||
| chr11:43789059 | T | C | 1 | a0001c0003t0001g0239 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.284-9261T>C | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 3/10 | chr11 | 43789059 | |||||||
| chr11:43789063 | G | C | 4 | a0001c0001t0001g0060 a0001c0001t0001g0061 a0001c0001t0001g0062 others(1): Show |
4 | HG02300.hp2 HG03453.hp2 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.284-9257G>C | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 3/10 | chr11 | 43789063 | |||||||
| chr11:43789067 | G | C | 3 | a0003c0004t0001g0241 a0003c0004t0001g0249 a0003c0004t0001g0264 |
3 | HG02647.hp2 HG03516.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.284-9253G>C | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 3/10 | chr11 | 43789067 | |||||||
| chr11:43789527 | C | A | 18 | a0001c0001t0001g0060 a0001c0001t0001g0061 a0001c0001t0001g0062 others(15): Show |
18 | HG00280.hp1 HG00609.hp2 HG02300.hp2 others(15): Show |
intron_variant | MODIFIER | c.284-8793C>A | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 3/10 | chr11 | 43789527 | |||||||
| chr11:43789669 | T | C | 18 | a0001c0001t0001g0060 a0001c0001t0001g0061 a0001c0001t0001g0062 others(15): Show |
18 | HG00280.hp1 HG00609.hp2 HG02300.hp2 others(15): Show |
intron_variant | MODIFIER | c.284-8651T>C | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 3/10 | chr11 | 43789669 | |||||||
| chr11:43789683 | T | A | 1 | a0002c0002t0009g0200 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.284-8637T>A | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 3/10 | chr11 | 43789683 | |||||||
| chr11:43789775 | C | T | 3 | a0002c0002t0002g0180 a0004c0005t0002g0011 a0004c0005t0002g0012 |
3 | HG01099.hp2 HG01106.hp2 HG01258.hp1 |
intron_variant | MODIFIER | c.284-8545C>T | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 3/10 | chr11 | 43789775 | |||||||
| chr11:43789917 | G | A | 93 | a0001c0001t0001g0002 a0001c0001t0001g0026 a0001c0001t0001g0028 others(90): Show |
94 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(91): Show |
intron_variant | MODIFIER | c.284-8403G>A | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 3/10 | chr11 | 43789917 | |||||||
| chr11:43789932 | A | G | 38 | a0002c0002t0002g0004 a0002c0002t0002g0027 a0002c0002t0002g0109 others(35): Show |
38 | HG00280.hp2 HG00423.hp1 HG00738.hp1 others(35): Show |
intron_variant | MODIFIER | c.284-8388A>G | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 3/10 | chr11 | 43789932 | |||||||
| chr11:43790093 | C | G | 12 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(9): Show |
12 | HG01261.hp2 HG01884.hp2 HG02257.hp1 others(9): Show |
intron_variant | MODIFIER | c.284-8227C>G | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 3/10 | chr11 | 43790093 | |||||||
| chr11:43790512 | G | C | 2 | a0001c0001t0001g0042 a0001c0001t0001g0057 |
2 | HG00735.hp2 HG02683.hp2 |
intron_variant | MODIFIER | c.284-7808G>C | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 3/10 | chr11 | 43790512 | |||||||
| chr11:43790681 | G | A | 21 | a0001c0001t0001g0186 a0001c0001t0001g0208 a0001c0001t0001g0209 others(18): Show |
21 | HG00099.hp2 HG00140.hp1 HG01167.hp2 others(18): Show |
intron_variant | MODIFIER | c.284-7639G>A | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 3/10 | chr11 | 43790681 | |||||||
| chr11:43791014 | TA | T | 18 | a0001c0001t0001g0060 a0001c0001t0001g0061 a0001c0001t0001g0062 others(15): Show |
18 | HG00280.hp1 HG00609.hp2 HG02300.hp2 others(15): Show |
intron_variant | MODIFIER | c.284-7297delA | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr11 | 43791014 | ||||||
| chr11:43791015 | A | T | 1 | a0001c0003t0001g0238 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.284-7305A>T | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 3/10 | chr11 | 43791015 | |||||||
| chr11:43791267 | C | T | 5 | a0001c0001t0001g0111 a0001c0001t0001g0112 a0001c0001t0001g0202 others(2): Show |
5 | HG02055.hp1 HG02559.hp2 HG02809.hp2 others(2): Show |
intron_variant | MODIFIER | c.284-7053C>T | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 3/10 | chr11 | 43791267 | |||||||
| chr11:43791489 | A | G | 18 | a0001c0001t0001g0060 a0001c0001t0001g0061 a0001c0001t0001g0062 others(15): Show |
18 | HG00280.hp1 HG00609.hp2 HG02300.hp2 others(15): Show |
intron_variant | MODIFIER | c.284-6831A>G | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 3/10 | chr11 | 43791489 | |||||||
| chr11:43791647 | G | A | 18 | a0001c0001t0001g0060 a0001c0001t0001g0061 a0001c0001t0001g0062 others(15): Show |
18 | HG00280.hp1 HG00609.hp2 HG02300.hp2 others(15): Show |
intron_variant | MODIFIER | c.284-6673G>A | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 3/10 | chr11 | 43791647 | |||||||
| chr11:43791676 | G | A | 1 | a0001c0001t0001g0084 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.284-6644G>A | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 3/10 | chr11 | 43791676 | |||||||
| chr11:43791838 | A | G | 14 | a0001c0001t0003g0013 a0001c0001t0003g0014 a0001c0001t0003g0015 others(11): Show |
14 | HG00280.hp1 HG00609.hp2 NA18612.hp2 others(11): Show |
intron_variant | MODIFIER | c.284-6482A>G | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 3/10 | chr11 | 43791838 | |||||||
| chr11:43792000 | G | A | 2 | a0001c0001t0001g0006 a0001c0001t0001g0010 |
2 | HG02257.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.284-6320G>A | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 3/10 | chr11 | 43792000 | |||||||
| chr11:43792134 | G | A | 4 | a0001c0001t0001g0060 a0001c0001t0001g0061 a0001c0001t0001g0062 others(1): Show |
4 | HG02300.hp2 HG03453.hp2 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.284-6186G>A | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 3/10 | chr11 | 43792134 | |||||||
| chr11:43792171 | G | A | 1 | a0001c0001t0003g0013 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.284-6149G>A | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 3/10 | chr11 | 43792171 | |||||||
| chr11:43792226 | T | G | 220 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(217): Show |
221 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(218): Show |
intron_variant | MODIFIER | c.284-6094T>G | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 3/10 | chr11 | 43792226 | |||||||
| chr11:43792262 | G | T | 2 | a0001c0001t0001g0069 a0001c0001t0001g0105 |
2 | HG01928.hp1 NA19000.hp2 |
intron_variant | MODIFIER | c.284-6058G>T | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 3/10 | chr11 | 43792262 | |||||||
| chr11:43792525 | A | T | 2 | a0001c0001t0001g0006 a0001c0001t0001g0010 |
2 | HG02257.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.284-5795A>T | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 3/10 | chr11 | 43792525 | |||||||
| chr11:43792644 | A | G | 12 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(9): Show |
12 | HG01261.hp2 HG01884.hp2 HG02257.hp1 others(9): Show |
intron_variant | MODIFIER | c.284-5676A>G | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 3/10 | chr11 | 43792644 | |||||||
| chr11:43792682 | C | CT | 63 | a0001c0001t0001g0002 a0001c0001t0001g0032 a0001c0001t0001g0088 others(60): Show |
64 | HG00280.hp1 HG00609.hp2 HG01070.hp2 others(61): Show |
intron_variant | MODIFIER | c.284-5616dupT | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr11 | 43792682 | ||||||
| chr11:43792682 | C | CTT | 34 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(31): Show |
34 | HG00140.hp1 HG01167.hp2 HG01168.hp2 others(31): Show |
intron_variant | MODIFIER | c.284-5617_284-5616d others(4): Show |
HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr11 | 43792682 | ||||||
| chr11:43792682 | C | CTTT | 22 | a0001c0001t0001g0128 a0001c0001t0001g0129 a0001c0001t0001g0215 others(19): Show |
22 | HG00099.hp2 HG00639.hp2 HG00642.hp2 others(19): Show |
intron_variant | MODIFIER | c.284-5618_284-5616d others(5): Show |
HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr11 | 43792682 | ||||||
| chr11:43792682 | CT | C | 34 | a0001c0001t0001g0028 a0001c0001t0001g0050 a0001c0001t0001g0060 others(31): Show |
34 | HG00280.hp2 HG00423.hp1 HG00738.hp1 others(31): Show |
intron_variant | MODIFIER | c.284-5616delT | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr11 | 43792682 | ||||||
| chr11:43792740 | C | A | 1 | a0001c0001t0001g0094 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.284-5580C>A | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 3/10 | chr11 | 43792740 | |||||||
| chr11:43793020 | G | A | 2 | a0001c0001t0001g0034 a0001c0001t0001g0071 |
2 | NA18945.hp2 NA18982.hp1 |
intron_variant | MODIFIER | c.284-5300G>A | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 3/10 | chr11 | 43793020 | |||||||
| chr11:43793104 | C | T | 1 | a0002c0002t0002g0184 | 1 | NA19001.hp1 | intron_variant | MODIFIER | c.284-5216C>T | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 3/10 | chr11 | 43793104 | |||||||
| chr11:43793572 | A | G | 1 | a0001c0007t0001g0230 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.284-4748A>G | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 3/10 | chr11 | 43793572 | |||||||
| chr11:43793654 | G | A | 1 | a0002c0002t0002g0277 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.284-4666G>A | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 3/10 | chr11 | 43793654 | |||||||
| chr11:43793707 | G | T | 1 | a0001c0001t0001g0093 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.284-4613G>T | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 3/10 | chr11 | 43793707 | |||||||
| chr11:43793708 | G | C | 1 | a0001c0001t0001g0093 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.284-4612G>C | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 3/10 | chr11 | 43793708 | |||||||
| chr11:43793710 | T | C | 1 | a0001c0001t0001g0093 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.284-4610T>C | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 3/10 | chr11 | 43793710 | |||||||
| chr11:43793711 | C | A | 1 | a0001c0001t0001g0093 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.284-4609C>A | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 3/10 | chr11 | 43793711 | |||||||
| chr11:43793715 | T | G | 1 | a0001c0001t0001g0093 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.284-4605T>G | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 3/10 | chr11 | 43793715 | |||||||
| chr11:43793716 | C | A | 1 | a0001c0001t0001g0093 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.284-4604C>A | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 3/10 | chr11 | 43793716 | |||||||
| chr11:43793867 | C | T | 13 | a0001c0001t0003g0267 a0001c0001t0003g0268 a0001c0001t0003g0278 others(10): Show |
13 | HG01070.hp2 HG01071.hp1 HG02004.hp1 others(10): Show |
intron_variant | MODIFIER | c.284-4453C>T | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 3/10 | chr11 | 43793867 | |||||||
| chr11:43794050 | A | G | 54 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(51): Show |
54 | HG00099.hp2 HG00140.hp1 HG00639.hp2 others(51): Show |
intron_variant | MODIFIER | c.284-4270A>G | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 3/10 | chr11 | 43794050 | |||||||
| chr11:43794167 | A | G | 71 | a0001c0001t0001g0026 a0001c0001t0001g0028 a0001c0001t0001g0029 others(68): Show |
71 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(68): Show |
intron_variant | MODIFIER | c.284-4153A>G | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 3/10 | chr11 | 43794167 | |||||||
| chr11:43794256 | A | G | 54 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(51): Show |
54 | HG00099.hp2 HG00140.hp1 HG00639.hp2 others(51): Show |
intron_variant | MODIFIER | c.284-4064A>G | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 3/10 | chr11 | 43794256 | |||||||
| chr11:43794317 | A | C | 3 | a0001c0001t0001g0060 a0001c0001t0001g0061 a0001c0001t0001g0062 |
3 | HG03453.hp2 HG03471.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.284-4003A>C | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 3/10 | chr11 | 43794317 | |||||||
| chr11:43794513 | C | T | 14 | a0001c0001t0003g0013 a0001c0001t0003g0014 a0001c0001t0003g0015 others(11): Show |
14 | HG00280.hp1 HG00609.hp2 NA18612.hp2 others(11): Show |
intron_variant | MODIFIER | c.284-3807C>T | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 3/10 | chr11 | 43794513 | |||||||
| chr11:43794650 | C | T | 164 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(161): Show |
165 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(162): Show |
intron_variant | MODIFIER | c.284-3670C>T | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 3/10 | chr11 | 43794650 | |||||||
| chr11:43794845 | G | A | 2 | a0002c0002t0002g0192 a0002c0002t0002g0194 |
2 | HG03516.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.284-3475G>A | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 3/10 | chr11 | 43794845 | |||||||
| chr11:43795024 | G | GA | 54 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(51): Show |
54 | HG00099.hp2 HG00140.hp1 HG00639.hp2 others(51): Show |
intron_variant | MODIFIER | c.284-3288dupA | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr11 | 43795024 | ||||||
| chr11:43795059 | A | G | 93 | a0001c0001t0001g0002 a0001c0001t0001g0026 a0001c0001t0001g0028 others(90): Show |
94 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(91): Show |
intron_variant | MODIFIER | c.284-3261A>G | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 3/10 | chr11 | 43795059 | |||||||
| chr11:43795091 | C | T | 1 | a0001c0007t0001g0230 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.284-3229C>T | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 3/10 | chr11 | 43795091 | |||||||
| chr11:43795575 | C | T | 164 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(161): Show |
165 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(162): Show |
intron_variant | MODIFIER | c.284-2745C>T | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 3/10 | chr11 | 43795575 | |||||||
| chr11:43795634 | C | T | 21 | a0001c0001t0001g0186 a0001c0001t0001g0208 a0001c0001t0001g0209 others(18): Show |
21 | HG00099.hp2 HG00140.hp1 HG01167.hp2 others(18): Show |
intron_variant | MODIFIER | c.284-2686C>T | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 3/10 | chr11 | 43795634 | |||||||
| chr11:43795635 | G | A | 12 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(9): Show |
12 | HG01261.hp2 HG01884.hp2 HG02257.hp1 others(9): Show |
intron_variant | MODIFIER | c.284-2685G>A | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 3/10 | chr11 | 43795635 | |||||||
| chr11:43795770 | C | G | 163 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(160): Show |
164 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(161): Show |
intron_variant | MODIFIER | c.284-2550C>G | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 3/10 | chr11 | 43795770 | |||||||
| chr11:43795812 | A | G | 72 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(69): Show |
72 | HG00099.hp2 HG00140.hp1 HG00639.hp2 others(69): Show |
intron_variant | MODIFIER | c.284-2508A>G | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 3/10 | chr11 | 43795812 | |||||||
| chr11:43795820 | G | A | 4 | a0002c0002t0002g0250 a0002c0002t0002g0251 a0002c0002t0002g0252 others(1): Show |
4 | HG01891.hp1 HG02280.hp2 HG06807.hp2 others(1): Show |
intron_variant | MODIFIER | c.284-2500G>A | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 3/10 | chr11 | 43795820 | |||||||
| chr11:43795913 | G | C | 1 | a0002c0002t0002g0110 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.284-2407G>C | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 3/10 | chr11 | 43795913 | |||||||
| chr11:43796044 | C | G | 1 | a0001c0001t0003g0206 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.284-2276C>G | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 3/10 | chr11 | 43796044 | |||||||
| chr11:43796148 | A | G | 1 | a0002c0002t0002g0072 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.284-2172A>G | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 3/10 | chr11 | 43796148 | |||||||
| chr11:43796161 | G | A | 1 | a0002c0002t0002g0132 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.284-2159G>A | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 3/10 | chr11 | 43796161 | |||||||
| chr11:43796180 | C | A | 182 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(179): Show |
183 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(180): Show |
intron_variant | MODIFIER | c.284-2140C>A | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 3/10 | chr11 | 43796180 | |||||||
| chr11:43796232 | A | G | 2 | a0001c0001t0001g0106 a0001c0001t0001g0196 |
2 | NA18943.hp1 NA18953.hp1 |
intron_variant | MODIFIER | c.284-2088A>G | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 3/10 | chr11 | 43796232 | |||||||
| chr11:43796276 | G | A | 1 | a0001c0001t0001g0026 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.284-2044G>A | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 3/10 | chr11 | 43796276 | |||||||
| chr11:43796332 | T | G | 1 | a0001c0007t0001g0230 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.284-1988T>G | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 3/10 | chr11 | 43796332 | |||||||
| chr11:43796505 | T | C | 54 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(51): Show |
54 | HG00099.hp2 HG00140.hp1 HG00639.hp2 others(51): Show |
intron_variant | MODIFIER | c.284-1815T>C | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 3/10 | chr11 | 43796505 | |||||||
| chr11:43796844 | C | CT | 164 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(161): Show |
165 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(162): Show |
intron_variant | MODIFIER | c.284-1467dupT | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr11 | 43796844 | ||||||
| chr11:43796976 | T | C | 4 | a0002c0002t0002g0161 a0002c0002t0002g0176 a0002c0002t0002g0177 others(1): Show |
4 | HG02723.hp1 HG03130.hp2 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.284-1344T>C | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 3/10 | chr11 | 43796976 | |||||||
| chr11:43797224 | G | A | 1 | a0001c0003t0001g0235 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.284-1096G>A | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 3/10 | chr11 | 43797224 | |||||||
| chr11:43797273 | C | G | 14 | a0001c0001t0003g0013 a0001c0001t0003g0014 a0001c0001t0003g0015 others(11): Show |
14 | HG00280.hp1 HG00609.hp2 NA18612.hp2 others(11): Show |
intron_variant | MODIFIER | c.284-1047C>G | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 3/10 | chr11 | 43797273 | |||||||
| chr11:43797414 | C | T | 2 | a0002c0002t0004g0205 a0002c0002t0004g0274 |
2 | HG02451.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.284-906C>T | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 3/10 | chr11 | 43797414 | |||||||
| chr11:43797814 | T | C | 4 | a0001c0001t0001g0028 a0001c0001t0001g0050 a0001c0001t0001g0056 others(1): Show |
4 | HG02155.hp1 HG03704.hp1 HG03834.hp1 others(1): Show |
intron_variant | MODIFIER | c.284-506T>C | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 3/10 | chr11 | 43797814 | |||||||
| chr11:43797887 | G | A | 4 | a0001c0001t0001g0060 a0001c0001t0001g0061 a0001c0001t0001g0062 others(1): Show |
4 | HG02300.hp2 HG03453.hp2 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.284-433G>A | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 3/10 | chr11 | 43797887 | |||||||
| chr11:43797957 | A | G | 3 | a0001c0001t0001g0265 a0001c0001t0001g0266 a0001c0001t0001g0270 |
3 | HG02451.hp2 HG02630.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.284-363A>G | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 3/10 | chr11 | 43797957 | |||||||
| chr11:43798064 | A | G | 1 | a0001c0007t0001g0230 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.284-256A>G | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 3/10 | chr11 | 43798064 | |||||||
| chr11:43798453 | G | GTATTTA | 14 | a0001c0001t0003g0013 a0001c0001t0003g0014 a0001c0001t0003g0015 others(11): Show |
14 | HG00280.hp1 HG00609.hp2 NA18612.hp2 others(11): Show |
intron_variant | MODIFIER | c.391+27_391+28insAT others(4): Show |
HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr11 | 43798453 | ||||||
| chr11:43798456 | C | A | 14 | a0001c0001t0003g0013 a0001c0001t0003g0014 a0001c0001t0003g0015 others(11): Show |
14 | HG00280.hp1 HG00609.hp2 NA18612.hp2 others(11): Show |
intron_variant | MODIFIER | c.391+29C>A | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 4/10 | chr11 | 43798456 | |||||||
| chr11:43798658 | C | A | 53 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(50): Show |
53 | HG00099.hp2 HG00140.hp1 HG00639.hp2 others(50): Show |
intron_variant | MODIFIER | c.391+231C>A | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 4/10 | chr11 | 43798658 | |||||||
| chr11:43798698 | A | G | 5 | a0001c0001t0001g0005 a0001c0001t0001g0007 a0001c0001t0001g0008 others(2): Show |
5 | HG01261.hp2 HG02809.hp1 HG02886.hp2 others(2): Show |
intron_variant | MODIFIER | c.391+271A>G | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 4/10 | chr11 | 43798698 | |||||||
| chr11:43798762 | G | T | 4 | a0001c0001t0001g0060 a0001c0001t0001g0061 a0001c0001t0001g0062 others(1): Show |
4 | HG02300.hp2 HG03453.hp2 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.391+335G>T | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 4/10 | chr11 | 43798762 | |||||||
| chr11:43798926 | T | C | 182 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(179): Show |
183 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(180): Show |
intron_variant | MODIFIER | c.391+499T>C | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 4/10 | chr11 | 43798926 | |||||||
| chr11:43798974 | C | T | 182 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(179): Show |
183 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(180): Show |
intron_variant | MODIFIER | c.391+547C>T | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 4/10 | chr11 | 43798974 | |||||||
| chr11:43799169 | A | G | 93 | a0001c0001t0001g0002 a0001c0001t0001g0026 a0001c0001t0001g0028 others(90): Show |
94 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(91): Show |
intron_variant | MODIFIER | c.391+742A>G | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 4/10 | chr11 | 43799169 | |||||||
| chr11:43799279 | A | T | 2 | a0001c0001t0001g0009 a0001c0001t0001g0226 |
2 | HG01261.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.391+852A>T | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 4/10 | chr11 | 43799279 | |||||||
| chr11:43799454 | G | T | 182 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(179): Show |
183 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(180): Show |
intron_variant | MODIFIER | c.391+1027G>T | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 4/10 | chr11 | 43799454 | |||||||
| chr11:43799708 | A | G | 1 | a0001c0001t0001g0036 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.391+1281A>G | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 4/10 | chr11 | 43799708 | |||||||
| chr11:43799805 | C | T | 4 | a0001c0001t0001g0060 a0001c0001t0001g0061 a0001c0001t0001g0062 others(1): Show |
4 | HG02300.hp2 HG03453.hp2 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.391+1378C>T | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 4/10 | chr11 | 43799805 | |||||||
| chr11:43799857 | C | T | 16 | a0001c0001t0001g0002 a0001c0001t0001g0120 a0001c0001t0001g0121 others(13): Show |
17 | HG01109.hp1 HG01496.hp1 HG02258.hp2 others(14): Show |
intron_variant | MODIFIER | c.391+1430C>T | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 4/10 | chr11 | 43799857 | |||||||
| chr11:43800048 | C | T | 1 | a0001c0001t0001g0054 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.391+1621C>T | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 4/10 | chr11 | 43800048 | |||||||
| chr11:43800204 | A | C | 1 | a0001c0001t0003g0206 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.391+1777A>C | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 4/10 | chr11 | 43800204 | |||||||
| chr11:43800438 | A | C | 7 | a0001c0003t0003g0242 a0001c0003t0003g0243 a0001c0003t0003g0244 others(4): Show |
7 | HG01070.hp2 HG01071.hp1 HG02004.hp1 others(4): Show |
intron_variant | MODIFIER | c.391+2011A>C | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 4/10 | chr11 | 43800438 | |||||||
| chr11:43800509 | TG | T | 71 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(68): Show |
71 | HG00099.hp2 HG00140.hp1 HG00639.hp2 others(68): Show |
intron_variant | MODIFIER | c.391+2083delG | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 4/10 | chr11 | 43800509 | |||||||
| chr11:43800909 | C | T | 1 | a0001c0001t0001g0219 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.391+2482C>T | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 4/10 | chr11 | 43800909 | |||||||
| chr11:43800959 | C | T | 93 | a0001c0001t0001g0002 a0001c0001t0001g0026 a0001c0001t0001g0028 others(90): Show |
94 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(91): Show |
intron_variant | MODIFIER | c.391+2532C>T | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 4/10 | chr11 | 43800959 | |||||||
| chr11:43801038 | C | T | 1 | a0002c0002t0008g0003 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.391+2611C>T | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 4/10 | chr11 | 43801038 | |||||||
| chr11:43801087 | C | T | 14 | a0001c0001t0003g0013 a0001c0001t0003g0014 a0001c0001t0003g0015 others(11): Show |
14 | HG00280.hp1 HG00609.hp2 NA18612.hp2 others(11): Show |
intron_variant | MODIFIER | c.391+2660C>T | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 4/10 | chr11 | 43801087 | |||||||
| chr11:43801092 | T | C | 11 | a0002c0002t0002g0004 a0002c0002t0002g0138 a0002c0002t0002g0142 others(8): Show |
11 | HG01109.hp2 HG01884.hp1 HG02257.hp2 others(8): Show |
intron_variant | MODIFIER | c.391+2665T>C | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 4/10 | chr11 | 43801092 | |||||||
| chr11:43801144 | G | GA | 6 | a0001c0001t0001g0002 a0001c0001t0001g0120 a0001c0001t0001g0121 others(3): Show |
7 | HG01109.hp1 HG01496.hp1 HG02965.hp1 others(4): Show |
intron_variant | MODIFIER | c.391+2727dupA | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr11 | 43801144 | ||||||
| chr11:43801144 | GA | G | 14 | a0001c0001t0003g0013 a0001c0001t0003g0014 a0001c0001t0003g0015 others(11): Show |
14 | HG00280.hp1 HG00609.hp2 NA18612.hp2 others(11): Show |
intron_variant | MODIFIER | c.391+2727delA | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr11 | 43801144 | ||||||
| chr11:43801207 | T | C | 182 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(179): Show |
183 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(180): Show |
intron_variant | MODIFIER | c.391+2780T>C | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 4/10 | chr11 | 43801207 | |||||||
| chr11:43801208 | G | A | 72 | a0001c0001t0001g0026 a0001c0001t0001g0028 a0001c0001t0001g0029 others(69): Show |
72 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(69): Show |
intron_variant | MODIFIER | c.391+2781G>A | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 4/10 | chr11 | 43801208 | |||||||
| chr11:43801335 | A | G | 164 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(161): Show |
165 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(162): Show |
intron_variant | MODIFIER | c.391+2908A>G | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 4/10 | chr11 | 43801335 | |||||||
| chr11:43801593 | GAGATATA others(33): Show |
G | 164 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(161): Show |
165 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(162): Show |
intron_variant | MODIFIER | c.391+3168_391+3207d others(42): Show |
HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr11 | 43801593 | ||||||
| chr11:43801595 | G | GAT | 6 | a0001c0001t0003g0067 a0002c0002t0002g0170 a0002c0002t0002g0175 others(3): Show |
6 | HG00738.hp1 HG02647.hp1 HG03130.hp2 others(3): Show |
intron_variant | MODIFIER | c.391+3203_391+3204d others(4): Show |
HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr11 | 43801595 | ||||||
| chr11:43801595 | G | GATAT | 10 | a0001c0001t0003g0016 a0001c0001t0003g0017 a0001c0001t0003g0018 others(7): Show |
10 | HG00280.hp2 HG01099.hp1 HG01346.hp2 others(7): Show |
intron_variant | MODIFIER | c.391+3201_391+3204d others(6): Show |
HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr11 | 43801595 | ||||||
| chr11:43801595 | G | GATATAT | 8 | a0001c0001t0003g0014 a0001c0001t0003g0015 a0001c0001t0003g0022 others(5): Show |
8 | NA18944.hp2 NA18948.hp1 NA18960.hp1 others(5): Show |
intron_variant | MODIFIER | c.391+3199_391+3204d others(8): Show |
HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr11 | 43801595 | ||||||
| chr11:43801595 | G | GATATATA others(1): Show |
8 | a0001c0001t0003g0013 a0001c0001t0003g0020 a0002c0002t0002g0109 others(5): Show |
8 | HG00423.hp1 HG02080.hp2 HG02818.hp1 others(5): Show |
intron_variant | MODIFIER | c.391+3197_391+3204d others(10): Show |
HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr11 | 43801595 | ||||||
| chr11:43801595 | G | GATATATA others(3): Show |
2 | a0002c0002t0002g0027 a0005c0006t0012g0021 |
2 | HG00609.hp2 NA20905.hp2 |
intron_variant | MODIFIER | c.391+3195_391+3204d others(12): Show |
HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr11 | 43801595 | ||||||
| chr11:43801595 | G | GATATATA others(5): Show |
2 | a0001c0001t0003g0103 a0002c0002t0002g0253 |
2 | HG01891.hp1 NA19064.hp1 |
intron_variant | MODIFIER | c.391+3193_391+3204d others(14): Show |
HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr11 | 43801595 | ||||||
| chr11:43801595 | G | GATATATA others(3): Show |
1 | a0002c0002t0002g0132 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.391+3176_391+3177i others(12): Show |
HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr11 | 43801595 | ||||||
| chr11:43801595 | GAT | G | 7 | a0002c0002t0002g0148 a0002c0002t0002g0149 a0002c0002t0002g0158 others(4): Show |
7 | HG02155.hp2 HG02698.hp1 HG03516.hp1 others(4): Show |
intron_variant | MODIFIER | c.391+3203_391+3204d others(4): Show |
HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr11 | 43801595 | ||||||
| chr11:43801595 | GATAT | G | 30 | a0002c0002t0002g0001 a0002c0002t0002g0025 a0002c0002t0002g0037 others(27): Show |
31 | HG00140.hp2 HG00639.hp1 HG00642.hp1 others(28): Show |
intron_variant | MODIFIER | c.391+3201_391+3204d others(6): Show |
HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr11 | 43801595 | ||||||
| chr11:43801595 | GATATAT | G | 14 | a0002c0002t0002g0038 a0002c0002t0002g0117 a0002c0002t0002g0118 others(11): Show |
14 | HG00323.hp1 HG00408.hp2 HG00609.hp1 others(11): Show |
intron_variant | MODIFIER | c.391+3199_391+3204d others(8): Show |
HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr11 | 43801595 | ||||||
| chr11:43801595 | GATATATA others(3): Show |
G | 2 | a0002c0002t0002g0138 a0002c0002t0002g0154 |
2 | HG02257.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.391+3195_391+3204d others(12): Show |
HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr11 | 43801595 | ||||||
| chr11:43801595 | GATATATA others(5): Show |
G | 12 | a0002c0002t0002g0004 a0002c0002t0002g0116 a0002c0002t0002g0126 others(9): Show |
12 | HG01109.hp2 HG01884.hp1 HG02622.hp1 others(9): Show |
intron_variant | MODIFIER | c.391+3193_391+3204d others(14): Show |
HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr11 | 43801595 | ||||||
| chr11:43801977 | AT | A | 73 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(70): Show |
73 | HG00099.hp2 HG00140.hp1 HG00639.hp2 others(70): Show |
intron_variant | MODIFIER | c.391+3562delT | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr11 | 43801977 | ||||||
| chr11:43802048 | C | T | 1 | a0001c0001t0001g0054 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.391+3621C>T | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 4/10 | chr11 | 43802048 | |||||||
| chr11:43802059 | C | T | 1 | a0001c0001t0001g0053 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.391+3632C>T | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 4/10 | chr11 | 43802059 | |||||||
| chr11:43802208 | G | A | 14 | a0001c0001t0003g0013 a0001c0001t0003g0014 a0001c0001t0003g0015 others(11): Show |
14 | HG00280.hp1 HG00609.hp2 NA18612.hp2 others(11): Show |
intron_variant | MODIFIER | c.391+3781G>A | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 4/10 | chr11 | 43802208 | |||||||
| chr11:43802413 | A | T | 182 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(179): Show |
183 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(180): Show |
intron_variant | MODIFIER | c.391+3986A>T | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 4/10 | chr11 | 43802413 | |||||||
| chr11:43802757 | G | A | 18 | a0001c0001t0001g0060 a0001c0001t0001g0061 a0001c0001t0001g0062 others(15): Show |
18 | HG00280.hp1 HG00609.hp2 HG02300.hp2 others(15): Show |
intron_variant | MODIFIER | c.391+4330G>A | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 4/10 | chr11 | 43802757 | |||||||
| chr11:43802811 | T | C | 1 | a0001c0003t0001g0240 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.391+4384T>C | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 4/10 | chr11 | 43802811 | |||||||
| chr11:43802823 | G | A | 1 | a0001c0001t0001g0112 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.391+4396G>A | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 4/10 | chr11 | 43802823 | |||||||
| chr11:43803083 | A | T | 182 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(179): Show |
183 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(180): Show |
intron_variant | MODIFIER | c.391+4656A>T | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 4/10 | chr11 | 43803083 | |||||||
| chr11:43803228 | G | A | 53 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(50): Show |
53 | HG00099.hp2 HG00140.hp1 HG00639.hp2 others(50): Show |
intron_variant | MODIFIER | c.391+4801G>A | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 4/10 | chr11 | 43803228 | |||||||
| chr11:43803488 | C | T | 164 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(161): Show |
165 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(162): Show |
intron_variant | MODIFIER | c.391+5061C>T | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 4/10 | chr11 | 43803488 | |||||||
| chr11:43803596 | T | C | 93 | a0001c0001t0001g0002 a0001c0001t0001g0026 a0001c0001t0001g0028 others(90): Show |
94 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(91): Show |
intron_variant | MODIFIER | c.391+5169T>C | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 4/10 | chr11 | 43803596 | |||||||
| chr11:43803722 | A | G | 14 | a0001c0001t0003g0013 a0001c0001t0003g0014 a0001c0001t0003g0015 others(11): Show |
14 | HG00280.hp1 HG00609.hp2 NA18612.hp2 others(11): Show |
intron_variant | MODIFIER | c.391+5295A>G | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 4/10 | chr11 | 43803722 | |||||||
| chr11:43803816 | G | A | 72 | a0001c0001t0001g0026 a0001c0001t0001g0028 a0001c0001t0001g0029 others(69): Show |
72 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(69): Show |
intron_variant | MODIFIER | c.391+5389G>A | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 4/10 | chr11 | 43803816 | |||||||
| chr11:43803931 | C | T | 182 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(179): Show |
183 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(180): Show |
intron_variant | MODIFIER | c.391+5504C>T | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 4/10 | chr11 | 43803931 | |||||||
| chr11:43804045 | G | A | 93 | a0001c0001t0001g0002 a0001c0001t0001g0026 a0001c0001t0001g0028 others(90): Show |
94 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(91): Show |
intron_variant | MODIFIER | c.391+5618G>A | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 4/10 | chr11 | 43804045 | |||||||
| chr11:43804260 | G | A | 1 | a0001c0001t0001g0056 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.391+5833G>A | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 4/10 | chr11 | 43804260 | |||||||
| chr11:43804373 | C | T | 12 | a0002c0002t0002g0027 a0002c0002t0002g0132 a0002c0002t0002g0133 others(9): Show |
12 | HG00280.hp2 HG00738.hp1 HG01099.hp1 others(9): Show |
intron_variant | MODIFIER | c.391+5946C>T | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 4/10 | chr11 | 43804373 | |||||||
| chr11:43804443 | G | A | 1 | a0001c0007t0001g0230 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.391+6016G>A | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 4/10 | chr11 | 43804443 | |||||||
| chr11:43805030 | A | G | 2 | a0001c0001t0001g0006 a0001c0001t0001g0010 |
2 | HG02257.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.391+6603A>G | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 4/10 | chr11 | 43805030 | |||||||
| chr11:43805104 | G | A | 1 | a0001c0007t0001g0230 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.391+6677G>A | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 4/10 | chr11 | 43805104 | |||||||
| chr11:43805179 | A | G | 1 | a0002c0002t0002g0142 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.391+6752A>G | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 4/10 | chr11 | 43805179 | |||||||
| chr11:43805249 | G | GTAAATAC others(3): Show |
18 | a0001c0001t0003g0267 a0001c0001t0003g0268 a0001c0001t0003g0278 others(15): Show |
18 | HG01070.hp2 HG01071.hp1 HG02004.hp1 others(15): Show |
intron_variant | MODIFIER | c.391+6827_391+6836d others(12): Show |
HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr11 | 43805249 | ||||||
| chr11:43805321 | T | A | 4 | a0001c0001t0003g0267 a0001c0001t0003g0268 a0001c0001t0003g0278 others(1): Show |
4 | HG02572.hp1 HG02965.hp2 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.391+6894T>A | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 4/10 | chr11 | 43805321 | |||||||
| chr11:43805505 | A | G | 1 | a0001c0001t0001g0056 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.391+7078A>G | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 4/10 | chr11 | 43805505 | |||||||
| chr11:43805542 | G | A | 3 | a0001c0003t0001g0238 a0001c0003t0001g0239 a0001c0003t0001g0273 |
3 | HG00642.hp2 HG02735.hp2 HG04115.hp2 |
intron_variant | MODIFIER | c.391+7115G>A | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 4/10 | chr11 | 43805542 | |||||||
| chr11:43805622 | T | C | 1 | a0002c0002t0002g0165 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.391+7195T>C | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 4/10 | chr11 | 43805622 | |||||||
| chr11:43805701 | C | T | 2 | a0002c0002t0002g0039 a0002c0002t0002g0158 |
2 | HG02683.hp1 HG02698.hp1 |
intron_variant | MODIFIER | c.391+7274C>T | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 4/10 | chr11 | 43805701 | |||||||
| chr11:43805724 | T | G | 8 | a0001c0001t0001g0074 a0001c0001t0001g0076 a0001c0001t0001g0083 others(5): Show |
8 | HG02083.hp2 HG02698.hp2 NA18944.hp1 others(5): Show |
intron_variant | MODIFIER | c.391+7297T>G | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 4/10 | chr11 | 43805724 | |||||||
| chr11:43805887 | G | A | 1 | a0001c0001t0001g0036 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.391+7460G>A | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 4/10 | chr11 | 43805887 | |||||||
| chr11:43805961 | G | A | 1 | a0002c0002t0008g0003 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.391+7534G>A | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 4/10 | chr11 | 43805961 | |||||||
| chr11:43806095 | C | T | 1 | a0002c0002t0006g0108 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.391+7668C>T | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 4/10 | chr11 | 43806095 | |||||||
| chr11:43806384 | A | C | 13 | a0001c0001t0003g0267 a0001c0001t0003g0268 a0001c0001t0003g0278 others(10): Show |
13 | HG01070.hp2 HG01071.hp1 HG02004.hp1 others(10): Show |
intron_variant | MODIFIER | c.391+7957A>C | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 4/10 | chr11 | 43806384 | |||||||
| chr11:43806460 | G | A | 1 | a0002c0002t0002g0165 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.391+8033G>A | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 4/10 | chr11 | 43806460 | |||||||
| chr11:43806495 | A | G | 1 | a0001c0001t0001g0053 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.391+8068A>G | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 4/10 | chr11 | 43806495 | |||||||
| chr11:43806513 | A | G | 1 | a0001c0001t0001g0107 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.391+8086A>G | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 4/10 | chr11 | 43806513 | |||||||
| chr11:43806543 | A | C | 21 | a0001c0001t0001g0186 a0001c0001t0001g0208 a0001c0001t0001g0209 others(18): Show |
21 | HG00099.hp2 HG00140.hp1 HG01167.hp2 others(18): Show |
intron_variant | MODIFIER | c.391+8116A>C | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 4/10 | chr11 | 43806543 | |||||||
| chr11:43806544 | A | G | 53 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(50): Show |
53 | HG00099.hp2 HG00140.hp1 HG00639.hp2 others(50): Show |
intron_variant | MODIFIER | c.391+8117A>G | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 4/10 | chr11 | 43806544 | |||||||
| chr11:43806785 | A | C | 14 | a0002c0002t0002g0039 a0002c0002t0002g0127 a0002c0002t0002g0140 others(11): Show |
14 | HG00140.hp2 HG00735.hp1 HG01070.hp1 others(11): Show |
intron_variant | MODIFIER | c.391+8358A>C | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 4/10 | chr11 | 43806785 | |||||||
| chr11:43806840 | C | T | 1 | a0001c0001t0001g0046 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.391+8413C>T | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 4/10 | chr11 | 43806840 | |||||||
| chr11:43807009 | A | ACACTGTT others(2): Show |
182 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(179): Show |
183 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(180): Show |
intron_variant | MODIFIER | c.392-8425_392-8417d others(11): Show |
HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr11 | 43807009 | ||||||
| chr11:43807209 | G | A | 53 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(50): Show |
53 | HG00099.hp2 HG00140.hp1 HG00639.hp2 others(50): Show |
intron_variant | MODIFIER | c.392-8228G>A | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 4/10 | chr11 | 43807209 | |||||||
| chr11:43807262 | T | A | 2 | a0001c0001t0001g0006 a0001c0001t0001g0010 |
2 | HG02257.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.392-8175T>A | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 4/10 | chr11 | 43807262 | |||||||
| chr11:43807459 | G | A | 1 | a0001c0001t0001g0113 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.392-7978G>A | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 4/10 | chr11 | 43807459 | |||||||
| chr11:43807987 | A | G | 16 | a0001c0001t0001g0002 a0001c0001t0001g0120 a0001c0001t0001g0121 others(13): Show |
17 | HG01109.hp1 HG01496.hp1 HG02258.hp2 others(14): Show |
intron_variant | MODIFIER | c.392-7450A>G | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 4/10 | chr11 | 43807987 | |||||||
| chr11:43808058 | C | T | 1 | a0001c0001t0001g0266 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.392-7379C>T | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 4/10 | chr11 | 43808058 | |||||||
| chr11:43808290 | AT | A | 127 | a0001c0001t0001g0002 a0001c0001t0001g0026 a0001c0001t0001g0028 others(124): Show |
128 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(125): Show |
intron_variant | MODIFIER | c.392-7131delT | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr11 | 43808290 | ||||||
| chr11:43808931 | G | T | 2 | a0001c0003t0003g0231 a0001c0003t0003g0232 |
2 | HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.392-6506G>T | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 4/10 | chr11 | 43808931 | |||||||
| chr11:43809060 | A | G | 1 | a0002c0002t0008g0003 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.392-6377A>G | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 4/10 | chr11 | 43809060 | |||||||
| chr11:43809248 | G | A | 18 | a0001c0001t0001g0060 a0001c0001t0001g0061 a0001c0001t0001g0062 others(15): Show |
18 | HG00280.hp1 HG00609.hp2 HG02300.hp2 others(15): Show |
intron_variant | MODIFIER | c.392-6189G>A | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 4/10 | chr11 | 43809248 | |||||||
| chr11:43809345 | T | C | 1 | a0002c0002t0009g0200 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.392-6092T>C | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 4/10 | chr11 | 43809345 | |||||||
| chr11:43809521 | A | T | 1 | a0001c0001t0003g0206 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.392-5916A>T | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 4/10 | chr11 | 43809521 | |||||||
| chr11:43809593 | C | T | 14 | a0001c0001t0003g0013 a0001c0001t0003g0014 a0001c0001t0003g0015 others(11): Show |
14 | HG00280.hp1 HG00609.hp2 NA18612.hp2 others(11): Show |
intron_variant | MODIFIER | c.392-5844C>T | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 4/10 | chr11 | 43809593 | |||||||
| chr11:43809628 | G | T | 11 | a0002c0002t0002g0132 a0002c0002t0002g0133 a0002c0002t0002g0134 others(8): Show |
11 | HG00280.hp2 HG00738.hp1 HG01099.hp1 others(8): Show |
intron_variant | MODIFIER | c.392-5809G>T | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 4/10 | chr11 | 43809628 | |||||||
| chr11:43809636 | T | C | 1 | a0002c0002t0002g0275 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.392-5801T>C | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 4/10 | chr11 | 43809636 | |||||||
| chr11:43809684 | G | A | 1 | a0001c0001t0001g0080 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.392-5753G>A | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 4/10 | chr11 | 43809684 | |||||||
| chr11:43809772 | C | T | 1 | a0002c0002t0002g0141 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.392-5665C>T | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 4/10 | chr11 | 43809772 | |||||||
| chr11:43809961 | G | A | 18 | a0001c0001t0003g0267 a0001c0001t0003g0268 a0001c0001t0003g0278 others(15): Show |
18 | HG01070.hp2 HG01071.hp1 HG02004.hp1 others(15): Show |
intron_variant | MODIFIER | c.392-5476G>A | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 4/10 | chr11 | 43809961 | |||||||
| chr11:43810002 | G | A | 77 | a0001c0001t0001g0026 a0001c0001t0001g0028 a0001c0001t0001g0029 others(74): Show |
77 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(74): Show |
intron_variant | MODIFIER | c.392-5435G>A | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 4/10 | chr11 | 43810002 | |||||||
| chr11:43810022 | T | C | 3 | a0001c0001t0001g0032 a0001c0001t0001g0033 a0001c0001t0001g0125 |
3 | HG01884.hp2 HG02895.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.392-5415T>C | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 4/10 | chr11 | 43810022 | |||||||
| chr11:43810226 | A | G | 164 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(161): Show |
165 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(162): Show |
intron_variant | MODIFIER | c.392-5211A>G | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 4/10 | chr11 | 43810226 | |||||||
| chr11:43810312 | CT | C | 13 | a0001c0001t0003g0013 a0001c0001t0003g0014 a0001c0001t0003g0015 others(10): Show |
13 | HG00609.hp2 NA18612.hp2 NA18747.hp1 others(10): Show |
intron_variant | MODIFIER | c.392-5118delT | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr11 | 43810312 | ||||||
| chr11:43810367 | T | TTA | 3 | a0002c0002t0002g0131 a0002c0002t0002g0136 a0002c0002t0002g0184 |
3 | NA18943.hp2 NA18953.hp2 NA19001.hp1 |
intron_variant | MODIFIER | c.392-5035_392-5034d others(4): Show |
HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr11 | 43810367 | ||||||
| chr11:43810367 | T | TTATA | 6 | a0002c0002t0002g0137 a0002c0002t0002g0140 a0002c0002t0002g0141 others(3): Show |
6 | HG00140.hp2 HG01123.hp2 HG01358.hp1 others(3): Show |
intron_variant | MODIFIER | c.392-5037_392-5034d others(6): Show |
HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr11 | 43810367 | ||||||
| chr11:43810367 | T | TTATATA | 8 | a0002c0002t0002g0037 a0002c0002t0002g0064 a0002c0002t0002g0110 others(5): Show |
8 | HG00323.hp1 HG01070.hp1 HG01192.hp2 others(5): Show |
intron_variant | MODIFIER | c.392-5039_392-5034d others(8): Show |
HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr11 | 43810367 | ||||||
| chr11:43810367 | T | TTATATAT others(1): Show |
11 | a0002c0002t0002g0001 a0002c0002t0002g0025 a0002c0002t0002g0038 others(8): Show |
12 | HG00642.hp1 HG01069.hp2 HG01071.hp2 others(9): Show |
intron_variant | MODIFIER | c.392-5041_392-5034d others(10): Show |
HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr11 | 43810367 | ||||||
| chr11:43810367 | T | TTATATAT others(3): Show |
1 | a0002c0002t0002g0147 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.392-5043_392-5034d others(12): Show |
HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr11 | 43810367 | ||||||
| chr11:43810367 | T | TTATATAT others(5): Show |
5 | a0002c0002t0002g0072 a0002c0002t0002g0126 a0002c0002t0002g0154 others(2): Show |
5 | HG01884.hp1 HG01975.hp1 HG03225.hp2 others(2): Show |
intron_variant | MODIFIER | c.392-5045_392-5034d others(14): Show |
HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr11 | 43810367 | ||||||
| chr11:43810367 | T | TTATATAT others(7): Show |
2 | a0002c0002t0002g0172 a0002c0002t0002g0182 |
2 | NA18964.hp1 NA18969.hp1 |
intron_variant | MODIFIER | c.392-5047_392-5034d others(16): Show |
HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr11 | 43810367 | ||||||
| chr11:43810367 | T | TTATATAT others(9): Show |
5 | a0002c0002t0002g0116 a0002c0002t0002g0139 a0002c0002t0002g0153 others(2): Show |
5 | HG00639.hp1 HG01109.hp2 HG01258.hp1 others(2): Show |
intron_variant | MODIFIER | c.392-5049_392-5034d others(18): Show |
HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr11 | 43810367 | ||||||
| chr11:43810367 | T | TTATATAT others(11): Show |
4 | a0002c0002t0002g0135 a0002c0002t0002g0138 a0002c0002t0002g0144 others(1): Show |
4 | HG02257.hp2 HG03130.hp2 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.392-5051_392-5034d others(20): Show |
HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr11 | 43810367 | ||||||
| chr11:43810367 | T | TTATATAT others(13): Show |
6 | a0002c0002t0002g0004 a0002c0002t0002g0027 a0002c0002t0002g0156 others(3): Show |
6 | HG02622.hp1 HG02630.hp2 HG02647.hp1 others(3): Show |
intron_variant | MODIFIER | c.392-5053_392-5034d others(22): Show |
HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr11 | 43810367 | ||||||
| chr11:43810367 | T | TTATATAT others(15): Show |
7 | a0002c0002t0002g0109 a0002c0002t0002g0133 a0002c0002t0002g0134 others(4): Show |
7 | HG00423.hp1 HG02723.hp1 HG02818.hp1 others(4): Show |
intron_variant | MODIFIER | c.392-5055_392-5034d others(24): Show |
HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr11 | 43810367 | ||||||
| chr11:43810367 | T | TTATATAT others(17): Show |
2 | a0002c0002t0002g0142 a0002c0002t0002g0173 |
2 | HG02976.hp1 NA18944.hp2 |
intron_variant | MODIFIER | c.392-5057_392-5034d others(26): Show |
HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr11 | 43810367 | ||||||
| chr11:43810367 | T | TTATATAT others(19): Show |
1 | a0002c0002t0002g0191 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.392-5059_392-5034d others(28): Show |
HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr11 | 43810367 | ||||||
| chr11:43810367 | TTA | T | 3 | a0002c0002t0002g0193 a0002c0002t0002g0228 a0002c0002t0002g0275 |
3 | HG02559.hp1 HG02723.hp2 NA19063.hp1 |
intron_variant | MODIFIER | c.392-5035_392-5034d others(4): Show |
HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr11 | 43810367 | ||||||
| chr11:43810367 | TTATATA | T | 6 | a0002c0002t0002g0192 a0002c0002t0002g0194 a0002c0002t0002g0250 others(3): Show |
6 | HG01891.hp1 HG02280.hp2 HG03516.hp1 others(3): Show |
intron_variant | MODIFIER | c.392-5039_392-5034d others(8): Show |
HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr11 | 43810367 | ||||||
| chr11:43810367 | TTATATAT others(1): Show |
T | 7 | a0002c0002t0002g0132 a0002c0002t0002g0166 a0002c0002t0002g0167 others(4): Show |
7 | HG00280.hp2 HG00738.hp1 HG01099.hp1 others(4): Show |
intron_variant | MODIFIER | c.392-5041_392-5034d others(10): Show |
HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr11 | 43810367 | ||||||
| chr11:43810367 | TTATATAT others(3): Show |
T | 3 | a0001c0001t0001g0006 a0001c0001t0001g0010 a0002c0002t0002g0151 |
3 | HG02257.hp1 HG04184.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.392-5043_392-5034d others(12): Show |
HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr11 | 43810367 | ||||||
| chr11:43810367 | TTATATAT others(5): Show |
T | 1 | a0001c0001t0001g0073 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.392-5045_392-5034d others(14): Show |
HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr11 | 43810367 | ||||||
| chr11:43810367 | TTATATAT others(7): Show |
T | 92 | a0001c0001t0001g0002 a0001c0001t0001g0026 a0001c0001t0001g0028 others(89): Show |
93 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(90): Show |
intron_variant | MODIFIER | c.392-5047_392-5034d others(16): Show |
HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr11 | 43810367 | ||||||
| chr11:43810369 | A | T | 86 | a0001c0001t0001g0005 a0001c0001t0001g0007 a0001c0001t0001g0008 others(83): Show |
86 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(83): Show |
intron_variant | MODIFIER | c.392-5068A>T | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 4/10 | chr11 | 43810369 | |||||||
| chr11:43810379 | A | T | 2 | a0001c0001t0001g0006 a0001c0001t0001g0010 |
2 | HG02257.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.392-5058A>T | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 4/10 | chr11 | 43810379 | |||||||
| chr11:43810381 | A | T | 1 | a0001c0001t0001g0073 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.392-5056A>T | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 4/10 | chr11 | 43810381 | |||||||
| chr11:43810383 | A | T | 90 | a0001c0001t0001g0002 a0001c0001t0001g0026 a0001c0001t0001g0028 others(87): Show |
91 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(88): Show |
intron_variant | MODIFIER | c.392-5054A>T | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 4/10 | chr11 | 43810383 | |||||||
| chr11:43810390 | TATATATA others(7): Show |
T | 16 | a0001c0001t0003g0267 a0001c0001t0003g0268 a0001c0001t0003g0278 others(13): Show |
16 | HG01070.hp2 HG01071.hp1 HG02451.hp1 others(13): Show |
intron_variant | MODIFIER | c.392-5045_392-5032d others(16): Show |
HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr11 | 43810390 | ||||||
| chr11:43810392 | TATATATA others(5): Show |
T | 26 | a0001c0001t0001g0060 a0001c0001t0001g0061 a0001c0001t0001g0062 others(23): Show |
26 | HG00099.hp2 HG00140.hp1 HG01167.hp2 others(23): Show |
intron_variant | MODIFIER | c.392-5043_392-5032d others(14): Show |
HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr11 | 43810392 | ||||||
| chr11:43810394 | TATATATA others(3): Show |
T | 25 | a0001c0001t0001g0005 a0001c0001t0001g0007 a0001c0001t0001g0008 others(22): Show |
25 | HG00280.hp1 HG00609.hp2 HG01261.hp1 others(22): Show |
intron_variant | MODIFIER | c.392-5041_392-5032d others(12): Show |
HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr11 | 43810394 | ||||||
| chr11:43810396 | TATATATA others(1): Show |
T | 4 | a0001c0001t0001g0009 a0001c0001t0001g0226 a0001c0001t0001g0265 others(1): Show |
4 | HG01261.hp2 HG02630.hp1 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.392-5039_392-5032d others(10): Show |
HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr11 | 43810396 | ||||||
| chr11:43810398 | TATATAA | T | 13 | a0001c0001t0001g0128 a0001c0001t0001g0129 a0001c0001t0001g0266 others(10): Show |
13 | HG00639.hp2 HG00642.hp2 HG01069.hp1 others(10): Show |
intron_variant | MODIFIER | c.392-5037_392-5032d others(8): Show |
HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr11 | 43810398 | ||||||
| chr11:43810402 | T | A | 2 | a0002c0002t0002g0192 a0002c0002t0002g0194 |
2 | HG03516.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.392-5035T>A | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 4/10 | chr11 | 43810402 | |||||||
| chr11:43810403 | A | ATATATAT others(8): Show |
2 | a0002c0002t0002g0161 a0002c0002t0002g0261 |
2 | HG03139.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.392-5034_392-5033i others(17): Show |
HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 4/10 | chr11 | 43810403 | |||||||
| chr11:43810404 | A | T | 1 | a0003c0004t0001g0241 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.392-5033A>T | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 4/10 | chr11 | 43810404 | |||||||
| chr11:43810420 | C | T | 17 | a0001c0001t0003g0267 a0001c0001t0003g0268 a0001c0001t0003g0278 others(14): Show |
17 | HG01070.hp2 HG01071.hp1 HG02004.hp1 others(14): Show |
intron_variant | MODIFIER | c.392-5017C>T | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 4/10 | chr11 | 43810420 | |||||||
| chr11:43810464 | G | C | 3 | a0003c0004t0001g0241 a0003c0004t0001g0249 a0003c0004t0001g0264 |
3 | HG02647.hp2 HG03516.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.392-4973G>C | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 4/10 | chr11 | 43810464 | |||||||
| chr11:43810613 | T | C | 18 | a0001c0001t0003g0267 a0001c0001t0003g0268 a0001c0001t0003g0278 others(15): Show |
18 | HG01070.hp2 HG01071.hp1 HG02004.hp1 others(15): Show |
intron_variant | MODIFIER | c.392-4824T>C | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 4/10 | chr11 | 43810613 | |||||||
| chr11:43810746 | G | A | 19 | a0001c0001t0001g0128 a0001c0001t0001g0129 a0001c0001t0001g0265 others(16): Show |
19 | HG00639.hp2 HG00642.hp2 HG01069.hp1 others(16): Show |
intron_variant | MODIFIER | c.392-4691G>A | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 4/10 | chr11 | 43810746 | |||||||
| chr11:43810951 | G | A | 4 | a0001c0001t0003g0267 a0001c0001t0003g0268 a0001c0001t0003g0278 others(1): Show |
4 | HG02572.hp1 HG02965.hp2 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.392-4486G>A | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 4/10 | chr11 | 43810951 | |||||||
| chr11:43810955 | G | A | 164 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(161): Show |
165 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(162): Show |
intron_variant | MODIFIER | c.392-4482G>A | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 4/10 | chr11 | 43810955 | |||||||
| chr11:43811051 | A | G | 2 | a0002c0002t0004g0205 a0002c0002t0004g0274 |
2 | HG02451.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.392-4386A>G | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 4/10 | chr11 | 43811051 | |||||||
| chr11:43811184 | G | A | 1 | a0002c0002t0009g0200 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.392-4253G>A | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 4/10 | chr11 | 43811184 | |||||||
| chr11:43811967 | C | T | 1 | a0002c0002t0010g0157 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.392-3470C>T | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 4/10 | chr11 | 43811967 | |||||||
| chr11:43812174 | A | G | 4 | a0001c0001t0001g0060 a0001c0001t0001g0061 a0001c0001t0001g0062 others(1): Show |
4 | HG02300.hp2 HG03453.hp2 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.392-3263A>G | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 4/10 | chr11 | 43812174 | |||||||
| chr11:43812181 | C | T | 1 | a0001c0007t0001g0230 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.392-3256C>T | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 4/10 | chr11 | 43812181 | |||||||
| chr11:43812300 | T | C | 2 | a0001c0001t0001g0051 a0001c0001t0001g0052 |
2 | HG02004.hp2 HG02055.hp2 |
intron_variant | MODIFIER | c.392-3137T>C | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 4/10 | chr11 | 43812300 | |||||||
| chr11:43812366 | G | A | 1 | a0002c0002t0008g0003 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.392-3071G>A | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 4/10 | chr11 | 43812366 | |||||||
| chr11:43812386 | T | A | 93 | a0001c0001t0001g0002 a0001c0001t0001g0026 a0001c0001t0001g0028 others(90): Show |
94 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(91): Show |
intron_variant | MODIFIER | c.392-3051T>A | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 4/10 | chr11 | 43812386 | |||||||
| chr11:43812478 | G | A | 1 | a0002c0002t0002g0159 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.392-2959G>A | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 4/10 | chr11 | 43812478 | |||||||
| chr11:43812507 | G | C | 1 | a0001c0003t0003g0242 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.392-2930G>C | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 4/10 | chr11 | 43812507 | |||||||
| chr11:43812901 | G | T | 53 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(50): Show |
53 | HG00099.hp2 HG00140.hp1 HG00639.hp2 others(50): Show |
intron_variant | MODIFIER | c.392-2536G>T | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 4/10 | chr11 | 43812901 | |||||||
| chr11:43813290 | T | A | 1 | a0001c0001t0001g0006 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.392-2147T>A | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 4/10 | chr11 | 43813290 | |||||||
| chr11:43813291 | A | T | 16 | a0001c0001t0001g0002 a0001c0001t0001g0120 a0001c0001t0001g0121 others(13): Show |
17 | HG01109.hp1 HG01496.hp1 HG02258.hp2 others(14): Show |
intron_variant | MODIFIER | c.392-2146A>T | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 4/10 | chr11 | 43813291 | |||||||
| chr11:43813537 | TTTTG | T | 58 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(55): Show |
58 | HG00099.hp2 HG00140.hp1 HG00639.hp2 others(55): Show |
intron_variant | MODIFIER | c.392-1896_392-1893d others(6): Show |
HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr11 | 43813537 | ||||||
| chr11:43813761 | T | G | 1 | a0002c0002t0002g0162 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.392-1676T>G | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 4/10 | chr11 | 43813761 | |||||||
| chr11:43813936 | T | C | 1 | a0001c0001t0001g0113 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.392-1501T>C | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 4/10 | chr11 | 43813936 | |||||||
| chr11:43813957 | C | T | 1 | a0001c0001t0001g0113 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.392-1480C>T | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 4/10 | chr11 | 43813957 | |||||||
| chr11:43814019 | G | A | 3 | a0001c0001t0001g0050 a0001c0001t0001g0056 a0001c0001t0001g0059 |
3 | HG03704.hp1 HG03834.hp1 NA19005.hp2 |
intron_variant | MODIFIER | c.392-1418G>A | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 4/10 | chr11 | 43814019 | |||||||
| chr11:43814164 | AT | A | 78 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(75): Show |
79 | HG00099.hp2 HG00140.hp1 HG00639.hp2 others(76): Show |
intron_variant | MODIFIER | c.392-1262delT | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr11 | 43814164 | ||||||
| chr11:43814197 | G | C | 2 | a0002c0002t0004g0205 a0002c0002t0004g0274 |
2 | HG02451.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.392-1240G>C | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 4/10 | chr11 | 43814197 | |||||||
| chr11:43814207 | G | A | 1 | a0002c0002t0002g0144 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.392-1230G>A | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 4/10 | chr11 | 43814207 | |||||||
| chr11:43814289 | G | A | 5 | a0001c0001t0001g0111 a0001c0001t0001g0112 a0001c0001t0001g0202 others(2): Show |
5 | HG02055.hp1 HG02559.hp2 HG02809.hp2 others(2): Show |
intron_variant | MODIFIER | c.392-1148G>A | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 4/10 | chr11 | 43814289 | |||||||
| chr11:43814392 | A | G | 18 | a0001c0001t0001g0060 a0001c0001t0001g0061 a0001c0001t0001g0062 others(15): Show |
18 | HG00280.hp1 HG00609.hp2 HG02300.hp2 others(15): Show |
intron_variant | MODIFIER | c.392-1045A>G | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 4/10 | chr11 | 43814392 | |||||||
| chr11:43814455 | T | C | 1 | a0001c0001t0001g0214 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.392-982T>C | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 4/10 | chr11 | 43814455 | |||||||
| chr11:43814521 | G | A | 53 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(50): Show |
53 | HG00099.hp2 HG00140.hp1 HG00639.hp2 others(50): Show |
intron_variant | MODIFIER | c.392-916G>A | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 4/10 | chr11 | 43814521 | |||||||
| chr11:43814705 | T | C | 3 | a0001c0003t0001g0225 a0001c0003t0001g0227 a0001c0003t0001g0272 |
3 | HG00140.hp1 HG01167.hp2 NA20752.hp2 |
intron_variant | MODIFIER | c.392-732T>C | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 4/10 | chr11 | 43814705 | |||||||
| chr11:43814789 | A | G | 2 | a0004c0005t0002g0011 a0004c0005t0002g0012 |
2 | HG01099.hp2 HG01106.hp2 |
intron_variant | MODIFIER | c.392-648A>G | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 4/10 | chr11 | 43814789 | |||||||
| chr11:43814821 | T | C | 1 | a0001c0003t0001g0229 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.392-616T>C | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 4/10 | chr11 | 43814821 | |||||||
| chr11:43814906 | C | T | 7 | a0001c0003t0003g0242 a0001c0003t0003g0243 a0001c0003t0003g0244 others(4): Show |
7 | HG01070.hp2 HG01071.hp1 HG02004.hp1 others(4): Show |
intron_variant | MODIFIER | c.392-531C>T | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 4/10 | chr11 | 43814906 | |||||||
| chr11:43815046 | T | C | 164 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(161): Show |
165 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(162): Show |
intron_variant | MODIFIER | c.392-391T>C | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 4/10 | chr11 | 43815046 | |||||||
| chr11:43815062 | C | T | 93 | a0001c0001t0001g0002 a0001c0001t0001g0026 a0001c0001t0001g0028 others(90): Show |
94 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(91): Show |
intron_variant | MODIFIER | c.392-375C>T | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 4/10 | chr11 | 43815062 | |||||||
| chr11:43815103 | G | T | 2 | a0001c0003t0003g0231 a0001c0003t0003g0232 |
2 | HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.392-334G>T | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 4/10 | chr11 | 43815103 | |||||||
| chr11:43815162 | T | C | 1 | a0001c0001t0003g0206 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.392-275T>C | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 4/10 | chr11 | 43815162 | |||||||
| chr11:43815282 | T | C | 6 | a0002c0002t0002g0166 a0002c0002t0002g0167 a0002c0002t0002g0168 others(3): Show |
6 | HG00280.hp2 HG00738.hp1 HG01099.hp1 others(3): Show |
intron_variant | MODIFIER | c.392-155T>C | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 4/10 | chr11 | 43815282 | |||||||
| chr11:43815523 | A | G | 4 | a0001c0001t0001g0060 a0001c0001t0001g0061 a0001c0001t0001g0062 others(1): Show |
4 | HG02300.hp2 HG03453.hp2 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.456+22A>G | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 5/10 | chr11 | 43815523 | |||||||
| chr11:43815623 | T | C | 1 | a0001c0001t0003g0206 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.456+122T>C | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 5/10 | chr11 | 43815623 | |||||||
| chr11:43815696 | T | C | 2 | a0001c0001t0001g0042 a0001c0001t0001g0057 |
2 | HG00735.hp2 HG02683.hp2 |
intron_variant | MODIFIER | c.456+195T>C | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 5/10 | chr11 | 43815696 | |||||||
| chr11:43815804 | A | G | 6 | a0001c0001t0001g0002 a0001c0001t0001g0120 a0001c0001t0001g0121 others(3): Show |
7 | HG01109.hp1 HG01496.hp1 HG02965.hp1 others(4): Show |
intron_variant | MODIFIER | c.456+303A>G | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 5/10 | chr11 | 43815804 | |||||||
| chr11:43815848 | A | C | 1 | a0001c0001t0001g0255 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.456+347A>C | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 5/10 | chr11 | 43815848 | |||||||
| chr11:43815935 | G | A | 1 | a0002c0002t0004g0274 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.457-412G>A | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 5/10 | chr11 | 43815935 | |||||||
| chr11:43816001 | A | G | 164 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(161): Show |
165 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(162): Show |
intron_variant | MODIFIER | c.457-346A>G | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 5/10 | chr11 | 43816001 | |||||||
| chr11:43816039 | A | G | 1 | a0002c0002t0002g0250 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.457-308A>G | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 5/10 | chr11 | 43816039 | |||||||
| chr11:43816466 | T | C | 1 | a0002c0002t0002g0109 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.501+75T>C | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 6/10 | chr11 | 43816466 | |||||||
| chr11:43816574 | C | T | 2 | a0001c0001t0001g0041 a0001c0001t0001g0089 |
2 | NA18941.hp2 NA18966.hp1 |
intron_variant | MODIFIER | c.501+183C>T | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 6/10 | chr11 | 43816574 | |||||||
| chr11:43816585 | T | C | 13 | a0001c0001t0003g0267 a0001c0001t0003g0268 a0001c0001t0003g0278 others(10): Show |
13 | HG01070.hp2 HG01071.hp1 HG02004.hp1 others(10): Show |
intron_variant | MODIFIER | c.501+194T>C | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 6/10 | chr11 | 43816585 | |||||||
| chr11:43816767 | T | C | 164 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(161): Show |
165 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(162): Show |
intron_variant | MODIFIER | c.501+376T>C | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 6/10 | chr11 | 43816767 | |||||||
| chr11:43816791 | C | T | 5 | a0001c0001t0001g0209 a0001c0001t0001g0210 a0001c0001t0001g0211 others(2): Show |
5 | NA18966.hp2 NA18971.hp1 NA18973.hp1 others(2): Show |
intron_variant | MODIFIER | c.501+400C>T | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 6/10 | chr11 | 43816791 | |||||||
| chr11:43816890 | G | A | 27 | a0002c0002t0002g0027 a0002c0002t0002g0109 a0002c0002t0002g0116 others(24): Show |
27 | HG00280.hp2 HG00423.hp1 HG00738.hp1 others(24): Show |
intron_variant | MODIFIER | c.501+499G>A | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 6/10 | chr11 | 43816890 | |||||||
| chr11:43816980 | A | ATATATC | 3 | a0002c0002t0002g0153 a0002c0002t0002g0162 a0002c0002t0002g0251 |
3 | HG02622.hp1 HG02717.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.501+649_501+654dup others(6): Show |
HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr11 | 43816980 | ||||||
| chr11:43816980 | A | ATATATCT others(5): Show |
1 | a0002c0002t0002g0156 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.501+643_501+654dup others(12): Show |
HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr11 | 43816980 | ||||||
| chr11:43816980 | ATATATC | A | 41 | a0002c0002t0002g0001 a0002c0002t0002g0025 a0002c0002t0002g0037 others(38): Show |
42 | HG00323.hp1 HG00423.hp1 HG00642.hp1 others(39): Show |
intron_variant | MODIFIER | c.501+649_501+654del others(6): Show |
HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr11 | 43816980 | ||||||
| chr11:43816980 | ATATATCT others(5): Show |
A | 27 | a0002c0002t0002g0039 a0002c0002t0002g0064 a0002c0002t0002g0110 others(24): Show |
27 | HG00280.hp2 HG00408.hp2 HG00639.hp1 others(24): Show |
intron_variant | MODIFIER | c.501+643_501+654del others(12): Show |
HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr11 | 43816980 | ||||||
| chr11:43816980 | ATATATCT others(11): Show |
A | 8 | a0001c0001t0003g0013 a0001c0001t0003g0016 a0001c0001t0003g0017 others(5): Show |
8 | HG00609.hp2 NA18612.hp2 NA18747.hp1 others(5): Show |
intron_variant | MODIFIER | c.501+637_501+654del others(18): Show |
HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr11 | 43816980 | ||||||
| chr11:43816980 | ATATATCT others(17): Show |
A | 2 | a0001c0001t0003g0023 a0002c0002t0008g0003 |
2 | HG00280.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.501+631_501+654del others(24): Show |
HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr11 | 43816980 | ||||||
| chr11:43816980 | ATATATCT others(23): Show |
A | 1 | a0002c0002t0009g0200 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.501+625_501+654del others(30): Show |
HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr11 | 43816980 | ||||||
| chr11:43816980 | ATATATCT others(29): Show |
A | 16 | a0001c0001t0001g0053 a0001c0001t0001g0056 a0001c0001t0001g0059 others(13): Show |
16 | HG01070.hp2 HG01071.hp1 HG02004.hp1 others(13): Show |
intron_variant | MODIFIER | c.501+619_501+654del others(36): Show |
HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr11 | 43816980 | ||||||
| chr11:43816996 | ATCTATAT others(31): Show |
A | 1 | a0001c0001t0001g0029 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.501+607_501+644del others(38): Show |
HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr11 | 43816996 | ||||||
| chr11:43816998 | C | CTA | 4 | a0001c0001t0001g0060 a0001c0001t0001g0061 a0001c0001t0001g0062 others(1): Show |
4 | HG02300.hp2 HG03453.hp2 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.501+611_501+612dup others(2): Show |
HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr11 | 43816998 | ||||||
| chr11:43816998 | CTATATCT others(45): Show |
C | 16 | a0001c0001t0001g0002 a0001c0001t0001g0120 a0001c0001t0001g0121 others(13): Show |
17 | HG01109.hp1 HG01496.hp1 HG02258.hp2 others(14): Show |
intron_variant | MODIFIER | c.501+613_501+664del others(52): Show |
HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr11 | 43816998 | ||||||
| chr11:43817002 | ATCTATAT others(31): Show |
A | 21 | a0001c0001t0001g0030 a0001c0001t0001g0031 a0001c0001t0001g0035 others(18): Show |
21 | HG00099.hp1 HG00323.hp2 HG00735.hp2 others(18): Show |
intron_variant | MODIFIER | c.501+613_501+650del others(38): Show |
HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr11 | 43817002 | ||||||
| chr11:43817004 | CTATATCT others(19): Show |
C | 19 | a0001c0001t0001g0128 a0001c0001t0001g0129 a0001c0001t0001g0265 others(16): Show |
19 | HG00639.hp2 HG00642.hp2 HG01106.hp1 others(16): Show |
intron_variant | MODIFIER | c.501+617_501+642del others(26): Show |
HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr11 | 43817004 | ||||||
| chr11:43817004 | CTATATCT others(31): Show |
C | 50 | a0001c0001t0001g0026 a0001c0001t0001g0028 a0001c0001t0001g0034 others(47): Show |
50 | HG00408.hp1 HG00423.hp2 HG00738.hp2 others(47): Show |
intron_variant | MODIFIER | c.501+619_501+656del others(38): Show |
HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr11 | 43817004 | ||||||
| chr11:43817006 | ATATCTAT others(15): Show |
A | 1 | a0001c0003t0001g0235 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.501+619_501+640del others(22): Show |
HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr11 | 43817006 | ||||||
| chr11:43817006 | ATATCTAT others(21): Show |
A | 36 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(33): Show |
36 | HG00099.hp2 HG00140.hp1 HG01167.hp2 others(33): Show |
intron_variant | MODIFIER | c.501+619_501+646del others(28): Show |
HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr11 | 43817006 | ||||||
| chr11:43817010 | CTATATCT others(25): Show |
C | 2 | a0001c0001t0001g0093 a0001c0001t0001g0114 |
2 | HG02083.hp2 HG02523.hp1 |
intron_variant | MODIFIER | c.501+625_501+656del others(32): Show |
HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr11 | 43817010 | ||||||
| chr11:43817018 | ATATC | A | 4 | a0001c0001t0001g0060 a0001c0001t0001g0061 a0001c0001t0001g0062 others(1): Show |
4 | HG02300.hp2 HG03453.hp2 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.501+631_501+634del others(4): Show |
HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr11 | 43817018 | ||||||
| chr11:43817018 | ATATCTAT others(9): Show |
A | 5 | a0001c0001t0003g0014 a0001c0001t0003g0015 a0001c0001t0003g0018 others(2): Show |
5 | NA18945.hp1 NA18948.hp1 NA18960.hp1 others(2): Show |
intron_variant | MODIFIER | c.501+631_501+646del others(16): Show |
HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr11 | 43817018 | ||||||
| chr11:43817024 | ATATCTAT others(9): Show |
A | 1 | a0001c0001t0003g0103 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.501+637_501+652del others(16): Show |
HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr11 | 43817024 | ||||||
| chr11:43817028 | C | A | 4 | a0001c0001t0001g0060 a0001c0001t0001g0061 a0001c0001t0001g0062 others(1): Show |
4 | HG02300.hp2 HG03453.hp2 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.501+637C>A | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 6/10 | chr11 | 43817028 | |||||||
| chr11:43817030 | A | C | 1 | a0001c0003t0001g0235 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.501+639A>C | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 6/10 | chr11 | 43817030 | |||||||
| chr11:43817034 | C | A | 1 | a0002c0002t0008g0003 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.501+643C>A | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 6/10 | chr11 | 43817034 | |||||||
| chr11:43817034 | CTATATCT others(5): Show |
C | 1 | a0002c0002t0002g0187 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.501+649_501+660del others(12): Show |
HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr11 | 43817034 | ||||||
| chr11:43817036 | A | C | 36 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(33): Show |
36 | HG00099.hp2 HG00140.hp1 HG01167.hp2 others(33): Show |
intron_variant | MODIFIER | c.501+645A>C | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 6/10 | chr11 | 43817036 | |||||||
| chr11:43817038 | A | C | 19 | a0001c0001t0001g0128 a0001c0001t0001g0129 a0001c0001t0001g0265 others(16): Show |
19 | HG00639.hp2 HG00642.hp2 HG01106.hp1 others(16): Show |
intron_variant | MODIFIER | c.501+647A>C | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 6/10 | chr11 | 43817038 | |||||||
| chr11:43817040 | C | A | 44 | a0001c0001t0001g0029 a0001c0001t0001g0053 a0001c0001t0001g0056 others(41): Show |
44 | HG00280.hp1 HG00609.hp2 HG00639.hp2 others(41): Show |
intron_variant | MODIFIER | c.501+649C>A | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 6/10 | chr11 | 43817040 | |||||||
| chr11:43817053 | T | G | 1 | a0002c0002t0008g0003 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.501+662T>G | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 6/10 | chr11 | 43817053 | |||||||
| chr11:43817058 | A | C | 22 | a0002c0002t0002g0027 a0002c0002t0002g0109 a0002c0002t0002g0116 others(19): Show |
22 | HG00280.hp2 HG00423.hp1 HG00738.hp1 others(19): Show |
intron_variant | MODIFIER | c.501+667A>C | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 6/10 | chr11 | 43817058 | |||||||
| chr11:43817104 | A | G | 182 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(179): Show |
183 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(180): Show |
intron_variant | MODIFIER | c.501+713A>G | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 6/10 | chr11 | 43817104 | |||||||
| chr11:43817214 | G | A | 1 | a0001c0001t0001g0092 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.501+823G>A | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 6/10 | chr11 | 43817214 | |||||||
| chr11:43817474 | T | C | 1 | a0001c0001t0001g0005 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.501+1083T>C | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 6/10 | chr11 | 43817474 | |||||||
| chr11:43817793 | C | T | 1 | a0001c0003t0001g0235 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.501+1402C>T | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 6/10 | chr11 | 43817793 | |||||||
| chr11:43817881 | A | C | 72 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(69): Show |
72 | HG00099.hp2 HG00140.hp1 HG00639.hp2 others(69): Show |
intron_variant | MODIFIER | c.501+1490A>C | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 6/10 | chr11 | 43817881 | |||||||
| chr11:43818214 | C | T | 13 | a0001c0001t0003g0267 a0001c0001t0003g0268 a0001c0001t0003g0278 others(10): Show |
13 | HG01070.hp2 HG01071.hp1 HG02004.hp1 others(10): Show |
intron_variant | MODIFIER | c.501+1823C>T | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 6/10 | chr11 | 43818214 | |||||||
| chr11:43818385 | G | A | 182 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(179): Show |
183 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(180): Show |
intron_variant | MODIFIER | c.501+1994G>A | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 6/10 | chr11 | 43818385 | |||||||
| chr11:43819052 | T | A | 55 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(52): Show |
55 | HG00099.hp2 HG00140.hp1 HG00639.hp2 others(52): Show |
intron_variant | MODIFIER | c.501+2661T>A | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 6/10 | chr11 | 43819052 | |||||||
| chr11:43819067 | C | T | 1 | a0001c0001t0001g0257 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.501+2676C>T | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 6/10 | chr11 | 43819067 | |||||||
| chr11:43819189 | T | A | 1 | a0001c0003t0001g0235 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.501+2798T>A | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 6/10 | chr11 | 43819189 | |||||||
| chr11:43819371 | A | G | 1 | a0001c0001t0003g0014 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.501+2980A>G | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 6/10 | chr11 | 43819371 | |||||||
| chr11:43819996 | G | T | 1 | a0001c0001t0001g0006 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.501+3605G>T | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 6/10 | chr11 | 43819996 | |||||||
| chr11:43820244 | G | A | 4 | a0001c0001t0001g0060 a0001c0001t0001g0061 a0001c0001t0001g0062 others(1): Show |
4 | HG02300.hp2 HG03453.hp2 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.501+3853G>A | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 6/10 | chr11 | 43820244 | |||||||
| chr11:43820441 | A | G | 18 | a0001c0001t0001g0060 a0001c0001t0001g0061 a0001c0001t0001g0062 others(15): Show |
18 | HG00280.hp1 HG00609.hp2 HG02300.hp2 others(15): Show |
intron_variant | MODIFIER | c.501+4050A>G | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 6/10 | chr11 | 43820441 | |||||||
| chr11:43820499 | A | T | 4 | a0001c0001t0003g0267 a0001c0001t0003g0268 a0001c0001t0003g0278 others(1): Show |
4 | HG02572.hp1 HG02965.hp2 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.501+4108A>T | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 6/10 | chr11 | 43820499 | |||||||
| chr11:43820867 | G | A | 1 | a0002c0002t0002g0154 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.501+4476G>A | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 6/10 | chr11 | 43820867 | |||||||
| chr11:43820952 | A | T | 4 | a0001c0001t0003g0267 a0001c0001t0003g0268 a0001c0001t0003g0278 others(1): Show |
4 | HG02572.hp1 HG02965.hp2 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.501+4561A>T | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 6/10 | chr11 | 43820952 | |||||||
| chr11:43820968 | A | G | 2 | a0002c0002t0004g0205 a0002c0002t0004g0274 |
2 | HG02451.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.501+4577A>G | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 6/10 | chr11 | 43820968 | |||||||
| chr11:43821228 | A | G | 1 | a0001c0001t0001g0218 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.501+4837A>G | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 6/10 | chr11 | 43821228 | |||||||
| chr11:43821501 | C | T | 13 | a0001c0001t0003g0267 a0001c0001t0003g0268 a0001c0001t0003g0278 others(10): Show |
13 | HG01070.hp2 HG01071.hp1 HG02004.hp1 others(10): Show |
intron_variant | MODIFIER | c.501+5110C>T | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 6/10 | chr11 | 43821501 | |||||||
| chr11:43821651 | T | C | 164 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(161): Show |
165 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(162): Show |
intron_variant | MODIFIER | c.501+5260T>C | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 6/10 | chr11 | 43821651 | |||||||
| chr11:43821659 | A | G | 93 | a0001c0001t0001g0002 a0001c0001t0001g0026 a0001c0001t0001g0028 others(90): Show |
94 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(91): Show |
intron_variant | MODIFIER | c.501+5268A>G | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 6/10 | chr11 | 43821659 | |||||||
| chr11:43821788 | T | A | 1 | a0002c0002t0009g0200 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.501+5397T>A | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 6/10 | chr11 | 43821788 | |||||||
| chr11:43821899 | A | G | 1 | a0001c0001t0001g0257 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.501+5508A>G | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 6/10 | chr11 | 43821899 | |||||||
| chr11:43821952 | T | C | 6 | a0001c0001t0001g0002 a0001c0001t0001g0120 a0001c0001t0001g0121 others(3): Show |
7 | HG01109.hp1 HG01496.hp1 HG02965.hp1 others(4): Show |
intron_variant | MODIFIER | c.501+5561T>C | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 6/10 | chr11 | 43821952 | |||||||
| chr11:43822029 | C | G | 164 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(161): Show |
165 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(162): Show |
intron_variant | MODIFIER | c.501+5638C>G | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 6/10 | chr11 | 43822029 | |||||||
| chr11:43822419 | G | A | 13 | a0001c0001t0003g0267 a0001c0001t0003g0268 a0001c0001t0003g0278 others(10): Show |
13 | HG01070.hp2 HG01071.hp1 HG02004.hp1 others(10): Show |
intron_variant | MODIFIER | c.501+6028G>A | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 6/10 | chr11 | 43822419 | |||||||
| chr11:43822449 | A | G | 4 | a0001c0001t0003g0267 a0001c0001t0003g0268 a0001c0001t0003g0278 others(1): Show |
4 | HG02572.hp1 HG02965.hp2 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.501+6058A>G | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 6/10 | chr11 | 43822449 | |||||||
| chr11:43822630 | C | G | 18 | a0001c0001t0001g0060 a0001c0001t0001g0061 a0001c0001t0001g0062 others(15): Show |
18 | HG00280.hp1 HG00609.hp2 HG02300.hp2 others(15): Show |
intron_variant | MODIFIER | c.501+6239C>G | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 6/10 | chr11 | 43822630 | |||||||
| chr11:43822650 | C | A | 182 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(179): Show |
183 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(180): Show |
intron_variant | MODIFIER | c.501+6259C>A | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 6/10 | chr11 | 43822650 | |||||||
| chr11:43822950 | C | T | 164 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(161): Show |
165 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(162): Show |
intron_variant | MODIFIER | c.501+6559C>T | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 6/10 | chr11 | 43822950 | |||||||
| chr11:43823357 | A | G | 4 | a0001c0001t0001g0060 a0001c0001t0001g0061 a0001c0001t0001g0062 others(1): Show |
4 | HG02300.hp2 HG03453.hp2 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.501+6966A>G | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 6/10 | chr11 | 43823357 | |||||||
| chr11:43823373 | C | T | 1 | a0001c0007t0001g0230 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.501+6982C>T | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 6/10 | chr11 | 43823373 | |||||||
| chr11:43823688 | G | A | 2 | a0001c0001t0003g0013 a0001c0001t0003g0019 |
2 | NA19005.hp1 NA19007.hp1 |
intron_variant | MODIFIER | c.502-7288G>A | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 6/10 | chr11 | 43823688 | |||||||
| chr11:43823733 | A | T | 1 | a0001c0001t0001g0215 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.502-7243A>T | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 6/10 | chr11 | 43823733 | |||||||
| chr11:43823824 | C | T | 4 | a0001c0001t0001g0060 a0001c0001t0001g0061 a0001c0001t0001g0062 others(1): Show |
4 | HG02300.hp2 HG03453.hp2 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.502-7152C>T | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 6/10 | chr11 | 43823824 | |||||||
| chr11:43823869 | G | A | 1 | a0002c0002t0002g0039 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.502-7107G>A | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 6/10 | chr11 | 43823869 | |||||||
| chr11:43823895 | G | A | 1 | a0002c0002t0008g0003 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.502-7081G>A | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 6/10 | chr11 | 43823895 | |||||||
| chr11:43824048 | GA | G | 53 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(50): Show |
53 | HG00099.hp2 HG00140.hp1 HG00639.hp2 others(50): Show |
intron_variant | MODIFIER | c.502-6927delA | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 6/10 | chr11 | 43824048 | |||||||
| chr11:43824263 | G | C | 14 | a0001c0001t0003g0013 a0001c0001t0003g0014 a0001c0001t0003g0015 others(11): Show |
14 | HG00280.hp1 HG00609.hp2 NA18612.hp2 others(11): Show |
intron_variant | MODIFIER | c.502-6713G>C | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 6/10 | chr11 | 43824263 | |||||||
| chr11:43824290 | T | G | 1 | a0001c0003t0001g0229 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.502-6686T>G | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 6/10 | chr11 | 43824290 | |||||||
| chr11:43824348 | C | G | 1 | a0001c0001t0001g0097 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.502-6628C>G | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 6/10 | chr11 | 43824348 | |||||||
| chr11:43824503 | G | A | 1 | a0001c0001t0001g0100 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.502-6473G>A | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 6/10 | chr11 | 43824503 | |||||||
| chr11:43824567 | C | G | 1 | a0002c0002t0002g0250 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.502-6409C>G | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 6/10 | chr11 | 43824567 | |||||||
| chr11:43824957 | C | G | 18 | a0001c0001t0001g0060 a0001c0001t0001g0061 a0001c0001t0001g0062 others(15): Show |
18 | HG00280.hp1 HG00609.hp2 HG02300.hp2 others(15): Show |
intron_variant | MODIFIER | c.502-6019C>G | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 6/10 | chr11 | 43824957 | |||||||
| chr11:43825008 | G | A | 1 | a0001c0001t0001g0030 | 1 | HG01258.hp2 | intron_variant | MODIFIER | c.502-5968G>A | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 6/10 | chr11 | 43825008 | |||||||
| chr11:43825130 | C | CA | 148 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(145): Show |
149 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(146): Show |
intron_variant | MODIFIER | c.502-5832dupA | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr11 | 43825130 | ||||||
| chr11:43825147 | T | C | 18 | a0001c0001t0003g0267 a0001c0001t0003g0268 a0001c0001t0003g0278 others(15): Show |
18 | HG01070.hp2 HG01071.hp1 HG02004.hp1 others(15): Show |
intron_variant | MODIFIER | c.502-5829T>C | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 6/10 | chr11 | 43825147 | |||||||
| chr11:43825155 | A | G | 182 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(179): Show |
183 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(180): Show |
intron_variant | MODIFIER | c.502-5821A>G | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 6/10 | chr11 | 43825155 | |||||||
| chr11:43825300 | T | C | 182 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(179): Show |
183 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(180): Show |
intron_variant | MODIFIER | c.502-5676T>C | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 6/10 | chr11 | 43825300 | |||||||
| chr11:43825555 | G | A | 1 | a0001c0001t0001g0044 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.502-5421G>A | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 6/10 | chr11 | 43825555 | |||||||
| chr11:43825651 | C | A | 1 | a0001c0001t0003g0206 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.502-5325C>A | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 6/10 | chr11 | 43825651 | |||||||
| chr11:43825939 | AATT | A | 164 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(161): Show |
165 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(162): Show |
intron_variant | MODIFIER | c.502-5033_502-5031d others(5): Show |
HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr11 | 43825939 | ||||||
| chr11:43826081 | C | CT | 25 | a0001c0001t0001g0113 a0001c0001t0003g0014 a0001c0001t0003g0015 others(22): Show |
25 | HG00280.hp1 HG00609.hp2 HG01109.hp2 others(22): Show |
intron_variant | MODIFIER | c.502-4876dupT | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr11 | 43826081 | ||||||
| chr11:43826081 | C | T | 1 | a0002c0002t0002g0149 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.502-4895C>T | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 6/10 | chr11 | 43826081 | |||||||
| chr11:43826085 | T | TC | 159 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(156): Show |
160 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(157): Show |
intron_variant | MODIFIER | c.502-4891_502-4890i others(3): Show |
HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 6/10 | chr11 | 43826085 | |||||||
| chr11:43826086 | T | C | 1 | a0001c0001t0001g0220 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.502-4890T>C | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 6/10 | chr11 | 43826086 | |||||||
| chr11:43826089 | T | C | 1 | a0001c0001t0001g0152 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.502-4887T>C | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 6/10 | chr11 | 43826089 | |||||||
| chr11:43826090 | T | C | 92 | a0001c0001t0001g0002 a0001c0001t0001g0026 a0001c0001t0001g0028 others(89): Show |
93 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(90): Show |
intron_variant | MODIFIER | c.502-4886T>C | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 6/10 | chr11 | 43826090 | |||||||
| chr11:43826109 | G | T | 18 | a0001c0001t0001g0060 a0001c0001t0001g0061 a0001c0001t0001g0062 others(15): Show |
18 | HG00280.hp1 HG00609.hp2 HG02300.hp2 others(15): Show |
intron_variant | MODIFIER | c.502-4867G>T | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 6/10 | chr11 | 43826109 | |||||||
| chr11:43826143 | C | A | 1 | a0001c0003t0001g0233 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.502-4833C>A | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 6/10 | chr11 | 43826143 | |||||||
| chr11:43826163 | A | T | 1 | a0001c0001t0001g0087 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.502-4813A>T | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 6/10 | chr11 | 43826163 | |||||||
| chr11:43826361 | G | A | 164 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(161): Show |
165 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(162): Show |
intron_variant | MODIFIER | c.502-4615G>A | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 6/10 | chr11 | 43826361 | |||||||
| chr11:43826655 | AAT | A | 53 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(50): Show |
53 | HG00099.hp2 HG00140.hp1 HG00639.hp2 others(50): Show |
intron_variant | MODIFIER | c.502-4319_502-4318d others(4): Show |
HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr11 | 43826655 | ||||||
| chr11:43826752 | CTAAGAA | C | 14 | a0001c0001t0003g0013 a0001c0001t0003g0014 a0001c0001t0003g0015 others(11): Show |
14 | HG00280.hp1 HG00609.hp2 NA18612.hp2 others(11): Show |
intron_variant | MODIFIER | c.502-4222_502-4217d others(8): Show |
HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr11 | 43826752 | ||||||
| chr11:43826788 | G | A | 164 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(161): Show |
165 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(162): Show |
intron_variant | MODIFIER | c.502-4188G>A | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 6/10 | chr11 | 43826788 | |||||||
| chr11:43826889 | G | T | 20 | a0001c0001t0001g0208 a0001c0001t0001g0209 a0001c0001t0001g0210 others(17): Show |
20 | HG00099.hp2 HG00140.hp1 HG01167.hp2 others(17): Show |
intron_variant | MODIFIER | c.502-4087G>T | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 6/10 | chr11 | 43826889 | |||||||
| chr11:43827095 | C | T | 1 | a0002c0002t0009g0200 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.502-3881C>T | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 6/10 | chr11 | 43827095 | |||||||
| chr11:43827204 | C | A | 182 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(179): Show |
183 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(180): Show |
intron_variant | MODIFIER | c.502-3772C>A | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 6/10 | chr11 | 43827204 | |||||||
| chr11:43827253 | G | A | 1 | a0002c0002t0002g0039 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.502-3723G>A | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 6/10 | chr11 | 43827253 | |||||||
| chr11:43827326 | C | G | 1 | a0001c0001t0001g0032 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.502-3650C>G | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 6/10 | chr11 | 43827326 | |||||||
| chr11:43827327 | T | TA | 4 | a0001c0007t0001g0230 a0002c0002t0004g0205 a0002c0002t0004g0274 others(1): Show |
4 | HG02258.hp1 HG02451.hp1 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.502-3643dupA | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr11 | 43827327 | ||||||
| chr11:43827556 | A | G | 1 | a0001c0001t0001g0111 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.502-3420A>G | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 6/10 | chr11 | 43827556 | |||||||
| chr11:43827570 | A | G | 72 | a0001c0001t0001g0026 a0001c0001t0001g0028 a0001c0001t0001g0029 others(69): Show |
72 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(69): Show |
intron_variant | MODIFIER | c.502-3406A>G | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 6/10 | chr11 | 43827570 | |||||||
| chr11:43827743 | C | T | 182 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(179): Show |
183 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(180): Show |
intron_variant | MODIFIER | c.502-3233C>T | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 6/10 | chr11 | 43827743 | |||||||
| chr11:43828045 | T | C | 54 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(51): Show |
54 | HG00099.hp2 HG00140.hp1 HG00639.hp2 others(51): Show |
intron_variant | MODIFIER | c.502-2931T>C | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 6/10 | chr11 | 43828045 | |||||||
| chr11:43828074 | C | A | 2 | a0002c0002t0004g0205 a0002c0002t0004g0274 |
2 | HG02451.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.502-2902C>A | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 6/10 | chr11 | 43828074 | |||||||
| chr11:43828141 | C | CT | 9 | a0001c0001t0001g0009 a0001c0001t0001g0045 a0001c0001t0001g0082 others(6): Show |
9 | HG01258.hp1 HG01261.hp2 HG02080.hp2 others(6): Show |
intron_variant | MODIFIER | c.502-2816dupT | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr11 | 43828141 | ||||||
| chr11:43828141 | CT | C | 9 | a0001c0001t0001g0034 a0001c0001t0001g0076 a0001c0001t0001g0221 others(6): Show |
9 | HG01884.hp1 HG02602.hp1 HG02976.hp1 others(6): Show |
intron_variant | MODIFIER | c.502-2816delT | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr11 | 43828141 | ||||||
| chr11:43828256 | C | G | 1 | a0001c0003t0001g0227 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.502-2720C>G | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 6/10 | chr11 | 43828256 | |||||||
| chr11:43828334 | A | G | 182 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(179): Show |
183 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(180): Show |
intron_variant | MODIFIER | c.502-2642A>G | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 6/10 | chr11 | 43828334 | |||||||
| chr11:43828363 | C | T | 164 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(161): Show |
165 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(162): Show |
intron_variant | MODIFIER | c.502-2613C>T | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 6/10 | chr11 | 43828363 | |||||||
| chr11:43828437 | G | A | 2 | a0002c0002t0002g0139 a0002c0002t0002g0185 |
2 | HG00639.hp1 HG02572.hp2 |
intron_variant | MODIFIER | c.502-2539G>A | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 6/10 | chr11 | 43828437 | |||||||
| chr11:43828527 | A | G | 1 | a0001c0001t0001g0044 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.502-2449A>G | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 6/10 | chr11 | 43828527 | |||||||
| chr11:43828566 | C | T | 1 | a0002c0002t0002g0251 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.502-2410C>T | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 6/10 | chr11 | 43828566 | |||||||
| chr11:43828616 | CAA | C | 5 | a0002c0002t0002g0161 a0002c0002t0002g0175 a0002c0002t0002g0176 others(2): Show |
5 | HG02647.hp1 HG02723.hp1 HG03130.hp2 others(2): Show |
intron_variant | MODIFIER | c.502-2356_502-2355d others(4): Show |
HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr11 | 43828616 | ||||||
| chr11:43828873 | C | T | 16 | a0001c0001t0001g0002 a0001c0001t0001g0120 a0001c0001t0001g0121 others(13): Show |
17 | HG01109.hp1 HG01496.hp1 HG02258.hp2 others(14): Show |
intron_variant | MODIFIER | c.502-2103C>T | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 6/10 | chr11 | 43828873 | |||||||
| chr11:43829089 | A | G | 1 | a0001c0003t0001g0235 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.502-1887A>G | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 6/10 | chr11 | 43829089 | |||||||
| chr11:43829175 | T | C | 2 | a0001c0001t0001g0262 a0001c0001t0001g0263 |
2 | HG02258.hp2 HG02280.hp1 |
intron_variant | MODIFIER | c.502-1801T>C | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 6/10 | chr11 | 43829175 | |||||||
| chr11:43829189 | C | T | 1 | a0001c0001t0003g0206 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.502-1787C>T | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 6/10 | chr11 | 43829189 | |||||||
| chr11:43829736 | CTCCT | C | 18 | a0001c0001t0001g0060 a0001c0001t0001g0061 a0001c0001t0001g0062 others(15): Show |
18 | HG00280.hp1 HG00609.hp2 HG02300.hp2 others(15): Show |
intron_variant | MODIFIER | c.502-1234_502-1231d others(6): Show |
HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr11 | 43829736 | ||||||
| chr11:43829758 | G | T | 48 | a0001c0001t0001g0028 a0001c0001t0001g0034 a0001c0001t0001g0041 others(45): Show |
48 | HG00408.hp1 HG00423.hp2 HG00738.hp2 others(45): Show |
intron_variant | MODIFIER | c.502-1218G>T | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 6/10 | chr11 | 43829758 | |||||||
| chr11:43829797 | T | G | 1 | a0001c0001t0001g0055 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.502-1179T>G | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 6/10 | chr11 | 43829797 | |||||||
| chr11:43829924 | A | C | 164 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(161): Show |
165 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(162): Show |
intron_variant | MODIFIER | c.502-1052A>C | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 6/10 | chr11 | 43829924 | |||||||
| chr11:43829947 | T | C | 3 | a0001c0001t0001g0265 a0001c0001t0001g0266 a0001c0001t0001g0270 |
3 | HG02451.hp2 HG02630.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.502-1029T>C | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 6/10 | chr11 | 43829947 | |||||||
| chr11:43829948 | A | G | 2 | a0002c0002t0002g0171 a0002c0002t0002g0172 |
2 | NA18962.hp2 NA18969.hp1 |
intron_variant | MODIFIER | c.502-1028A>G | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 6/10 | chr11 | 43829948 | |||||||
| chr11:43830170 | T | C | 1 | a0002c0002t0010g0157 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.502-806T>C | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 6/10 | chr11 | 43830170 | |||||||
| chr11:43830213 | T | C | 1 | a0001c0001t0001g0256 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.502-763T>C | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 6/10 | chr11 | 43830213 | |||||||
| chr11:43830253 | G | A | 164 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(161): Show |
165 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(162): Show |
intron_variant | MODIFIER | c.502-723G>A | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 6/10 | chr11 | 43830253 | |||||||
| chr11:43830462 | T | G | 1 | a0001c0001t0001g0202 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.502-514T>G | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 6/10 | chr11 | 43830462 | |||||||
| chr11:43830533 | C | T | 2 | a0002c0002t0004g0205 a0002c0002t0004g0274 |
2 | HG02451.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.502-443C>T | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 6/10 | chr11 | 43830533 | |||||||
| chr11:43830547 | G | A | 12 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(9): Show |
12 | HG01261.hp2 HG01884.hp2 HG02257.hp1 others(9): Show |
intron_variant | MODIFIER | c.502-429G>A | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 6/10 | chr11 | 43830547 | |||||||
| chr11:43830630 | A | G | 21 | a0001c0001t0001g0186 a0001c0001t0001g0208 a0001c0001t0001g0209 others(18): Show |
21 | HG00099.hp2 HG00140.hp1 HG01167.hp2 others(18): Show |
intron_variant | MODIFIER | c.502-346A>G | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 6/10 | chr11 | 43830630 | |||||||
| chr11:43830820 | G | C | 5 | a0002c0002t0002g0161 a0002c0002t0002g0175 a0002c0002t0002g0176 others(2): Show |
5 | HG02647.hp1 HG02723.hp1 HG03130.hp2 others(2): Show |
intron_variant | MODIFIER | c.502-156G>C | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 6/10 | chr11 | 43830820 | |||||||
| chr11:43830941 | T | C | 93 | a0001c0001t0001g0002 a0001c0001t0001g0026 a0001c0001t0001g0028 others(90): Show |
94 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(91): Show |
intron_variant | MODIFIER | c.502-35T>C | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 6/10 | chr11 | 43830941 | |||||||
| chr11:43830955 | G | A | 1 | a0002c0002t0002g0187 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.502-21G>A | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 6/10 | chr11 | 43830955 | |||||||
| chr11:43831080 | C | T | 1 | a0001c0001t0001g0259 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.536+70C>T | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 7/10 | chr11 | 43831080 | |||||||
| chr11:43831339 | T | C | 14 | a0001c0001t0003g0267 a0001c0001t0003g0268 a0001c0001t0003g0278 others(11): Show |
14 | HG01070.hp2 HG01071.hp1 HG02004.hp1 others(11): Show |
intron_variant | MODIFIER | c.536+329T>C | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 7/10 | chr11 | 43831339 | |||||||
| chr11:43831376 | A | G | 6 | a0002c0002t0002g0109 a0002c0002t0002g0171 a0002c0002t0002g0172 others(3): Show |
6 | HG00423.hp1 NA18944.hp2 NA18962.hp2 others(3): Show |
intron_variant | MODIFIER | c.536+366A>G | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 7/10 | chr11 | 43831376 | |||||||
| chr11:43831511 | G | A | 1 | a0002c0002t0002g0275 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.536+501G>A | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 7/10 | chr11 | 43831511 | |||||||
| chr11:43831565 | A | G | 72 | a0001c0001t0001g0026 a0001c0001t0001g0028 a0001c0001t0001g0029 others(69): Show |
72 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(69): Show |
intron_variant | MODIFIER | c.536+555A>G | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 7/10 | chr11 | 43831565 | |||||||
| chr11:43831830 | T | C | 16 | a0001c0001t0001g0002 a0001c0001t0001g0120 a0001c0001t0001g0121 others(13): Show |
17 | HG01109.hp1 HG01496.hp1 HG02258.hp2 others(14): Show |
intron_variant | MODIFIER | c.536+820T>C | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 7/10 | chr11 | 43831830 | |||||||
| chr11:43832359 | T | C | 164 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(161): Show |
165 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(162): Show |
intron_variant | MODIFIER | c.536+1349T>C | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 7/10 | chr11 | 43832359 | |||||||
| chr11:43832458 | C | T | 1 | a0001c0001t0001g0254 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.536+1448C>T | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 7/10 | chr11 | 43832458 | |||||||
| chr11:43832471 | C | G | 2 | a0001c0001t0001g0063 a0001c0001t0001g0115 |
2 | NA19068.hp2 NA19084.hp1 |
intron_variant | MODIFIER | c.536+1461C>G | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 7/10 | chr11 | 43832471 | |||||||
| chr11:43832701 | C | A | 1 | a0001c0003t0001g0238 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.536+1691C>A | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 7/10 | chr11 | 43832701 | |||||||
| chr11:43832799 | G | T | 9 | a0001c0003t0003g0231 a0001c0003t0003g0232 a0001c0003t0003g0242 others(6): Show |
9 | HG01070.hp2 HG01071.hp1 HG02004.hp1 others(6): Show |
intron_variant | MODIFIER | c.536+1789G>T | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 7/10 | chr11 | 43832799 | |||||||
| chr11:43833032 | C | CA | 34 | a0002c0002t0002g0004 a0002c0002t0002g0027 a0002c0002t0002g0109 others(31): Show |
34 | HG00423.hp1 HG00738.hp1 HG01099.hp1 others(31): Show |
intron_variant | MODIFIER | c.536+2044dupA | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr11 | 43833032 | ||||||
| chr11:43833032 | CAAAAAA | C | 163 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(160): Show |
164 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(161): Show |
intron_variant | MODIFIER | c.536+2039_536+2044d others(8): Show |
HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr11 | 43833032 | ||||||
| chr11:43833060 | G | C | 164 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(161): Show |
165 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(162): Show |
intron_variant | MODIFIER | c.536+2050G>C | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 7/10 | chr11 | 43833060 | |||||||
| chr11:43833146 | A | G | 4 | a0001c0001t0001g0060 a0001c0001t0001g0061 a0001c0001t0001g0062 others(1): Show |
4 | HG02300.hp2 HG03453.hp2 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.536+2136A>G | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 7/10 | chr11 | 43833146 | |||||||
| chr11:43833360 | G | C | 73 | a0001c0001t0001g0026 a0001c0001t0001g0028 a0001c0001t0001g0029 others(70): Show |
73 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(70): Show |
intron_variant | MODIFIER | c.536+2350G>C | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 7/10 | chr11 | 43833360 | |||||||
| chr11:43833522 | A | G | 58 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(55): Show |
58 | HG00099.hp2 HG00140.hp1 HG00639.hp2 others(55): Show |
intron_variant | MODIFIER | c.536+2512A>G | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 7/10 | chr11 | 43833522 | |||||||
| chr11:43833739 | TTTG | T | 18 | a0001c0001t0001g0060 a0001c0001t0001g0061 a0001c0001t0001g0062 others(15): Show |
18 | HG00280.hp1 HG00609.hp2 HG02300.hp2 others(15): Show |
intron_variant | MODIFIER | c.536+2738_536+2740d others(5): Show |
HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr11 | 43833739 | ||||||
| chr11:43833758 | C | T | 3 | a0002c0002t0004g0205 a0002c0002t0004g0274 a0002c0002t0009g0200 |
3 | HG02451.hp1 HG02970.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.536+2748C>T | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 7/10 | chr11 | 43833758 | |||||||
| chr11:43833940 | A | G | 1 | a0001c0001t0001g0050 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.536+2930A>G | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 7/10 | chr11 | 43833940 | |||||||
| chr11:43833943 | G | A | 2 | a0002c0002t0002g0161 a0002c0002t0002g0176 |
2 | HG03130.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.536+2933G>A | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 7/10 | chr11 | 43833943 | |||||||
| chr11:43834243 | C | T | 1 | a0001c0001t0001g0051 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.536+3233C>T | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 7/10 | chr11 | 43834243 | |||||||
| chr11:43834368 | AT | A | 153 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(150): Show |
153 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(150): Show |
intron_variant | MODIFIER | c.536+3371delT | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr11 | 43834368 | ||||||
| chr11:43834574 | A | T | 4 | a0001c0001t0001g0060 a0001c0001t0001g0061 a0001c0001t0001g0062 others(1): Show |
4 | HG02300.hp2 HG03453.hp2 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.536+3564A>T | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 7/10 | chr11 | 43834574 | |||||||
| chr11:43834748 | A | G | 5 | a0001c0001t0001g0111 a0001c0001t0001g0112 a0001c0001t0001g0202 others(2): Show |
5 | HG02055.hp1 HG02559.hp2 HG02809.hp2 others(2): Show |
intron_variant | MODIFIER | c.537-3569A>G | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 7/10 | chr11 | 43834748 | |||||||
| chr11:43834771 | T | G | 94 | a0001c0001t0001g0002 a0001c0001t0001g0026 a0001c0001t0001g0028 others(91): Show |
95 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(92): Show |
intron_variant | MODIFIER | c.537-3546T>G | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 7/10 | chr11 | 43834771 | |||||||
| chr11:43834805 | G | T | 164 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(161): Show |
165 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(162): Show |
intron_variant | MODIFIER | c.537-3512G>T | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 7/10 | chr11 | 43834805 | |||||||
| chr11:43834885 | GT | G | 12 | a0002c0002t0002g0004 a0002c0002t0002g0138 a0002c0002t0002g0142 others(9): Show |
12 | HG01109.hp2 HG01884.hp1 HG02257.hp2 others(9): Show |
intron_variant | MODIFIER | c.537-3426delT | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr11 | 43834885 | ||||||
| chr11:43835613 | T | A | 14 | a0001c0003t0003g0231 a0001c0003t0003g0232 a0001c0003t0003g0242 others(11): Show |
14 | HG01070.hp2 HG01071.hp1 HG02004.hp1 others(11): Show |
intron_variant | MODIFIER | c.537-2704T>A | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 7/10 | chr11 | 43835613 | |||||||
| chr11:43835656 | G | C | 16 | a0001c0001t0001g0002 a0001c0001t0001g0120 a0001c0001t0001g0121 others(13): Show |
17 | HG01109.hp1 HG01496.hp1 HG02258.hp2 others(14): Show |
intron_variant | MODIFIER | c.537-2661G>C | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 7/10 | chr11 | 43835656 | |||||||
| chr11:43835868 | A | G | 162 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(159): Show |
163 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(160): Show |
intron_variant | MODIFIER | c.537-2449A>G | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 7/10 | chr11 | 43835868 | |||||||
| chr11:43835908 | A | G | 1 | a0001c0001t0001g0053 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.537-2409A>G | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 7/10 | chr11 | 43835908 | |||||||
| chr11:43836357 | G | T | 1 | a0002c0002t0002g0171 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.537-1960G>T | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 7/10 | chr11 | 43836357 | |||||||
| chr11:43836378 | G | C | 164 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(161): Show |
165 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(162): Show |
intron_variant | MODIFIER | c.537-1939G>C | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 7/10 | chr11 | 43836378 | |||||||
| chr11:43836725 | A | G | 1 | a0002c0002t0002g0161 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.537-1592A>G | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 7/10 | chr11 | 43836725 | |||||||
| chr11:43836748 | T | C | 3 | a0001c0001t0001g0029 a0001c0001t0001g0035 a0001c0001t0001g0048 |
3 | HG02135.hp2 NA19070.hp2 NA19090.hp2 |
intron_variant | MODIFIER | c.537-1569T>C | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 7/10 | chr11 | 43836748 | |||||||
| chr11:43836818 | A | G | 11 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(8): Show |
11 | HG01261.hp2 HG01884.hp2 HG02257.hp1 others(8): Show |
intron_variant | MODIFIER | c.537-1499A>G | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 7/10 | chr11 | 43836818 | |||||||
| chr11:43837001 | T | C | 4 | a0001c0001t0001g0060 a0001c0001t0001g0061 a0001c0001t0001g0062 others(1): Show |
4 | HG02300.hp2 HG03453.hp2 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.537-1316T>C | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 7/10 | chr11 | 43837001 | |||||||
| chr11:43837004 | G | A | 182 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(179): Show |
183 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(180): Show |
intron_variant | MODIFIER | c.537-1313G>A | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 7/10 | chr11 | 43837004 | |||||||
| chr11:43837132 | A | G | 182 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(179): Show |
183 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(180): Show |
intron_variant | MODIFIER | c.537-1185A>G | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 7/10 | chr11 | 43837132 | |||||||
| chr11:43837513 | C | T | 20 | a0001c0001t0001g0186 a0001c0001t0001g0208 a0001c0001t0001g0209 others(17): Show |
20 | HG00099.hp2 HG00140.hp1 HG01167.hp2 others(17): Show |
intron_variant | MODIFIER | c.537-804C>T | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 7/10 | chr11 | 43837513 | |||||||
| chr11:43837937 | G | C | 1 | a0001c0003t0001g0233 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.537-380G>C | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 7/10 | chr11 | 43837937 | |||||||
| chr11:43837969 | G | C | 2 | a0002c0002t0002g0177 a0002c0002t0002g0261 |
2 | HG02723.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.537-348G>C | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 7/10 | chr11 | 43837969 | |||||||
| chr11:43838066 | A | T | 1 | a0001c0003t0003g0242 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.537-251A>T | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 7/10 | chr11 | 43838066 | |||||||
| chr11:43838120 | A | T | 1 | a0001c0001t0001g0077 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.537-197A>T | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 7/10 | chr11 | 43838120 | |||||||
| chr11:43838467 | G | A | 4 | a0002c0002t0002g0117 a0002c0002t0002g0118 a0002c0002t0002g0119 others(1): Show |
4 | HG00408.hp2 HG02135.hp1 NA19084.hp2 others(1): Show |
intron_variant | MODIFIER | c.618+69G>A | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 8/10 | chr11 | 43838467 | |||||||
| chr11:43838650 | T | TC | 163 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(160): Show |
164 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(161): Show |
intron_variant | MODIFIER | c.618+258dupC | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 8/10 | INFO_REALIGN_3_PRIME | chr11 | 43838650 | ||||||
| chr11:43838750 | G | A | 77 | a0001c0001t0001g0026 a0001c0001t0001g0028 a0001c0001t0001g0029 others(74): Show |
77 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(74): Show |
intron_variant | MODIFIER | c.618+352G>A | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 8/10 | chr11 | 43838750 | |||||||
| chr11:43838840 | G | T | 1 | a0002c0002t0002g0141 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.618+442G>T | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 8/10 | chr11 | 43838840 | |||||||
| chr11:43839017 | G | A | 4 | a0001c0001t0003g0016 a0001c0001t0003g0017 a0001c0001t0003g0019 others(1): Show |
4 | NA18612.hp2 NA18747.hp1 NA18964.hp2 others(1): Show |
intron_variant | MODIFIER | c.618+619G>A | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 8/10 | chr11 | 43839017 | |||||||
| chr11:43839042 | G | A | 1 | a0002c0002t0004g0205 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.618+644G>A | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 8/10 | chr11 | 43839042 | |||||||
| chr11:43839093 | A | G | 1 | a0001c0001t0001g0256 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.618+695A>G | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 8/10 | chr11 | 43839093 | |||||||
| chr11:43839382 | A | C | 18 | a0001c0001t0003g0267 a0001c0001t0003g0268 a0001c0001t0003g0278 others(15): Show |
18 | HG01070.hp2 HG01071.hp1 HG02004.hp1 others(15): Show |
intron_variant | MODIFIER | c.619-617A>C | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 8/10 | chr11 | 43839382 | |||||||
| chr11:43839547 | C | G | 12 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(9): Show |
12 | HG01261.hp2 HG01884.hp2 HG02257.hp1 others(9): Show |
intron_variant | MODIFIER | c.619-452C>G | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 8/10 | chr11 | 43839547 | |||||||
| chr11:43839703 | T | C | 2 | a0001c0001t0001g0262 a0001c0001t0001g0263 |
2 | HG02258.hp2 HG02280.hp1 |
intron_variant | MODIFIER | c.619-296T>C | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 8/10 | chr11 | 43839703 | |||||||
| chr11:43839745 | G | T | 2 | a0001c0001t0001g0063 a0001c0001t0001g0115 |
2 | NA19068.hp2 NA19084.hp1 |
intron_variant | MODIFIER | c.619-254G>T | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 8/10 | chr11 | 43839745 | |||||||
| chr11:43839901 | G | A | 1 | a0002c0002t0002g0184 | 1 | NA19001.hp1 | intron_variant | MODIFIER | c.619-98G>A | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 8/10 | chr11 | 43839901 | |||||||
| chr11:43840198 | G | A | 163 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(160): Show |
164 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(161): Show |
intron_variant | MODIFIER | c.684+134G>A | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 9/10 | chr11 | 43840198 | |||||||
| chr11:43840387 | T | C | 1 | a0002c0002t0002g0187 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.684+323T>C | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 9/10 | chr11 | 43840387 | |||||||
| chr11:43840503 | A | G | 1 | a0001c0001t0001g0029 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.684+439A>G | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 9/10 | chr11 | 43840503 | |||||||
| chr11:43840570 | C | CACTAGTT others(3): Show |
19 | a0001c0001t0001g0060 a0001c0001t0001g0061 a0001c0001t0001g0062 others(16): Show |
19 | HG00280.hp1 HG00609.hp2 HG02300.hp2 others(16): Show |
intron_variant | MODIFIER | c.684+506_684+507ins others(10): Show |
HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 9/10 | chr11 | 43840570 | |||||||
| chr11:43840572 | A | T | 19 | a0001c0001t0001g0060 a0001c0001t0001g0061 a0001c0001t0001g0062 others(16): Show |
19 | HG00280.hp1 HG00609.hp2 HG02300.hp2 others(16): Show |
intron_variant | MODIFIER | c.684+508A>T | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 9/10 | chr11 | 43840572 | |||||||
| chr11:43840582 | A | G | 73 | a0001c0001t0001g0026 a0001c0001t0001g0028 a0001c0001t0001g0029 others(70): Show |
73 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(70): Show |
intron_variant | MODIFIER | c.684+518A>G | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 9/10 | chr11 | 43840582 | |||||||
| chr11:43840775 | T | C | 182 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(179): Show |
183 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(180): Show |
intron_variant | MODIFIER | c.684+711T>C | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 9/10 | chr11 | 43840775 | |||||||
| chr11:43840827 | A | G | 1 | a0001c0001t0001g0199 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.684+763A>G | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 9/10 | chr11 | 43840827 | |||||||
| chr11:43840958 | T | C | 3 | a0002c0002t0002g0131 a0002c0002t0002g0136 a0002c0002t0002g0137 |
3 | NA18943.hp2 NA18952.hp2 NA18953.hp2 |
intron_variant | MODIFIER | c.684+894T>C | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 9/10 | chr11 | 43840958 | |||||||
| chr11:43841326 | G | T | 19 | a0001c0001t0001g0060 a0001c0001t0001g0061 a0001c0001t0001g0062 others(16): Show |
19 | HG00280.hp1 HG00609.hp2 HG02300.hp2 others(16): Show |
intron_variant | MODIFIER | c.684+1262G>T | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 9/10 | chr11 | 43841326 | |||||||
| chr11:43841480 | G | A | 163 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(160): Show |
164 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(161): Show |
intron_variant | MODIFIER | c.684+1416G>A | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 9/10 | chr11 | 43841480 | |||||||
| chr11:43841607 | T | G | 2 | a0001c0001t0001g0075 a0001c0001t0001g0098 |
2 | NA18949.hp1 NA18960.hp2 |
intron_variant | MODIFIER | c.684+1543T>G | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 9/10 | chr11 | 43841607 | |||||||
| chr11:43841780 | C | T | 2 | a0001c0001t0001g0079 a0001c0001t0001g0080 |
2 | HG01123.hp1 NA20805.hp2 |
intron_variant | MODIFIER | c.684+1716C>T | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 9/10 | chr11 | 43841780 | |||||||
| chr11:43841793 | T | C | 19 | a0001c0001t0001g0060 a0001c0001t0001g0061 a0001c0001t0001g0062 others(16): Show |
19 | HG00280.hp1 HG00609.hp2 HG02300.hp2 others(16): Show |
intron_variant | MODIFIER | c.684+1729T>C | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 9/10 | chr11 | 43841793 | |||||||
| chr11:43841947 | C | A | 2 | a0001c0001t0001g0041 a0001c0001t0001g0089 |
2 | NA18941.hp2 NA18966.hp1 |
intron_variant | MODIFIER | c.684+1883C>A | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 9/10 | chr11 | 43841947 | |||||||
| chr11:43842156 | G | A | 1 | a0001c0001t0003g0020 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.684+2092G>A | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 9/10 | chr11 | 43842156 | |||||||
| chr11:43842305 | G | C | 3 | a0001c0001t0001g0029 a0001c0001t0001g0035 a0001c0001t0001g0048 |
3 | HG02135.hp2 NA19070.hp2 NA19090.hp2 |
intron_variant | MODIFIER | c.684+2241G>C | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 9/10 | chr11 | 43842305 | |||||||
| chr11:43842313 | A | C | 19 | a0001c0001t0001g0060 a0001c0001t0001g0061 a0001c0001t0001g0062 others(16): Show |
19 | HG00280.hp1 HG00609.hp2 HG02300.hp2 others(16): Show |
intron_variant | MODIFIER | c.684+2249A>C | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 9/10 | chr11 | 43842313 | |||||||
| chr11:43842326 | G | A | 19 | a0001c0001t0001g0060 a0001c0001t0001g0061 a0001c0001t0001g0062 others(16): Show |
19 | HG00280.hp1 HG00609.hp2 HG02300.hp2 others(16): Show |
intron_variant | MODIFIER | c.684+2262G>A | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 9/10 | chr11 | 43842326 | |||||||
| chr11:43842352 | G | A | 19 | a0001c0001t0001g0060 a0001c0001t0001g0061 a0001c0001t0001g0062 others(16): Show |
19 | HG00280.hp1 HG00609.hp2 HG02300.hp2 others(16): Show |
intron_variant | MODIFIER | c.684+2288G>A | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 9/10 | chr11 | 43842352 | |||||||
| chr11:43842352 | G | C | 2 | a0001c0001t0001g0088 a0001c0001t0001g0091 |
2 | HG00738.hp2 HG02738.hp2 |
intron_variant | MODIFIER | c.684+2288G>C | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 9/10 | chr11 | 43842352 | |||||||
| chr11:43842383 | C | T | 2 | a0001c0001t0001g0056 a0001c0001t0001g0059 |
2 | HG03704.hp1 HG03834.hp1 |
intron_variant | MODIFIER | c.684+2319C>T | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 9/10 | chr11 | 43842383 | |||||||
| chr11:43842540 | C | T | 3 | a0001c0001t0001g0032 a0001c0001t0001g0033 a0001c0001t0001g0125 |
3 | HG01884.hp2 HG02895.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.684+2476C>T | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 9/10 | chr11 | 43842540 | |||||||
| chr11:43842728 | T | C | 203 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(200): Show |
204 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(201): Show |
intron_variant | MODIFIER | c.684+2664T>C | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 9/10 | chr11 | 43842728 | |||||||
| chr11:43842894 | G | A | 1 | a0001c0001t0001g0215 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.684+2830G>A | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 9/10 | chr11 | 43842894 | |||||||
| chr11:43843391 | C | A | 8 | a0002c0002t0002g0127 a0002c0002t0002g0140 a0002c0002t0002g0147 others(5): Show |
8 | HG00140.hp2 HG01070.hp1 HG01167.hp1 others(5): Show |
intron_variant | MODIFIER | c.684+3327C>A | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 9/10 | chr11 | 43843391 | |||||||
| chr11:43843597 | GC | G | 6 | a0002c0002t0002g0004 a0002c0002t0002g0145 a0002c0002t0002g0153 others(3): Show |
6 | HG02622.hp1 HG02630.hp2 HG02717.hp1 others(3): Show |
intron_variant | MODIFIER | c.684+3536delC | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr11 | 43843597 | ||||||
| chr11:43843865 | C | A | 19 | a0001c0001t0001g0060 a0001c0001t0001g0061 a0001c0001t0001g0062 others(16): Show |
19 | HG00280.hp1 HG00609.hp2 HG02300.hp2 others(16): Show |
intron_variant | MODIFIER | c.684+3801C>A | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 9/10 | chr11 | 43843865 | |||||||
| chr11:43843910 | G | A | 1 | a0002c0002t0002g0126 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.684+3846G>A | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 9/10 | chr11 | 43843910 | |||||||
| chr11:43843947 | T | C | 5 | a0002c0002t0002g0161 a0002c0002t0002g0175 a0002c0002t0002g0176 others(2): Show |
5 | HG02647.hp1 HG02723.hp1 HG03130.hp2 others(2): Show |
intron_variant | MODIFIER | c.684+3883T>C | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 9/10 | chr11 | 43843947 | |||||||
| chr11:43843951 | A | G | 73 | a0001c0001t0001g0026 a0001c0001t0001g0028 a0001c0001t0001g0029 others(70): Show |
73 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(70): Show |
intron_variant | MODIFIER | c.684+3887A>G | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 9/10 | chr11 | 43843951 | |||||||
| chr11:43844164 | C | T | 1 | a0002c0002t0002g0039 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.684+4100C>T | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 9/10 | chr11 | 43844164 | |||||||
| chr11:43844169 | G | A | 1 | a0002c0002t0008g0003 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.684+4105G>A | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 9/10 | chr11 | 43844169 | |||||||
| chr11:43844338 | C | A | 1 | a0001c0001t0001g0208 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.684+4274C>A | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 9/10 | chr11 | 43844338 | |||||||
| chr11:43844687 | G | A | 1 | a0001c0001t0001g0006 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.684+4623G>A | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 9/10 | chr11 | 43844687 | |||||||
| chr11:43844744 | T | A | 163 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(160): Show |
164 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(161): Show |
intron_variant | MODIFIER | c.684+4680T>A | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 9/10 | chr11 | 43844744 | |||||||
| chr11:43844981 | G | GTTGT | 78 | a0001c0001t0001g0026 a0001c0001t0001g0028 a0001c0001t0001g0029 others(75): Show |
78 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(75): Show |
intron_variant | MODIFIER | c.684+4939_684+4942d others(6): Show |
HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr11 | 43844981 | ||||||
| chr11:43844981 | GTTGT | G | 12 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(9): Show |
12 | HG01261.hp2 HG01884.hp2 HG02257.hp1 others(9): Show |
intron_variant | MODIFIER | c.684+4939_684+4942d others(6): Show |
HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr11 | 43844981 | ||||||
| chr11:43845352 | T | C | 1 | a0001c0007t0001g0230 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.684+5288T>C | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 9/10 | chr11 | 43845352 | |||||||
| chr11:43845362 | T | C | 1 | a0001c0003t0001g0198 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.684+5298T>C | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 9/10 | chr11 | 43845362 | |||||||
| chr11:43845392 | C | T | 3 | a0001c0001t0001g0005 a0001c0001t0001g0007 a0001c0001t0001g0008 |
3 | HG02809.hp1 HG02886.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.684+5328C>T | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 9/10 | chr11 | 43845392 | |||||||
| chr11:43845470 | CTT | C | 163 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(160): Show |
164 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(161): Show |
intron_variant | MODIFIER | c.684+5409_684+5410d others(4): Show |
HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr11 | 43845470 | ||||||
| chr11:43845725 | C | T | 1 | a0001c0007t0001g0230 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.684+5661C>T | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 9/10 | chr11 | 43845725 | |||||||
| chr11:43845726 | G | A | 1 | a0001c0003t0001g0229 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.684+5662G>A | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 9/10 | chr11 | 43845726 | |||||||
| chr11:43846048 | G | T | 4 | a0001c0001t0001g0060 a0001c0001t0001g0061 a0001c0001t0001g0062 others(1): Show |
4 | HG02300.hp2 HG03453.hp2 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.684+5984G>T | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 9/10 | chr11 | 43846048 | |||||||
| chr11:43846098 | G | T | 1 | a0002c0002t0008g0003 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.684+6034G>T | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 9/10 | chr11 | 43846098 | |||||||
| chr11:43846102 | G | A | 163 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(160): Show |
164 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(161): Show |
intron_variant | MODIFIER | c.684+6038G>A | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 9/10 | chr11 | 43846102 | |||||||
| chr11:43846373 | G | A | 2 | a0002c0002t0002g0190 a0002c0002t0002g0191 |
2 | NA18982.hp2 NA19060.hp1 |
intron_variant | MODIFIER | c.684+6309G>A | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 9/10 | chr11 | 43846373 | |||||||
| chr11:43846392 | G | A | 19 | a0001c0001t0001g0060 a0001c0001t0001g0061 a0001c0001t0001g0062 others(16): Show |
19 | HG00280.hp1 HG00609.hp2 HG02300.hp2 others(16): Show |
intron_variant | MODIFIER | c.684+6328G>A | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 9/10 | chr11 | 43846392 | |||||||
| chr11:43846493 | G | A | 180 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(177): Show |
181 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(178): Show |
intron_variant | MODIFIER | c.684+6429G>A | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 9/10 | chr11 | 43846493 | |||||||
| chr11:43846818 | C | G | 220 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(217): Show |
221 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(218): Show |
intron_variant | MODIFIER | c.684+6754C>G | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 9/10 | chr11 | 43846818 | |||||||
| chr11:43846839 | C | T | 3 | a0001c0001t0001g0029 a0001c0001t0001g0035 a0001c0001t0001g0048 |
3 | HG02135.hp2 NA19070.hp2 NA19090.hp2 |
intron_variant | MODIFIER | c.684+6775C>T | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 9/10 | chr11 | 43846839 | |||||||
| chr11:43847031 | T | C | 16 | a0001c0001t0001g0002 a0001c0001t0001g0120 a0001c0001t0001g0121 others(13): Show |
17 | HG01109.hp1 HG01496.hp1 HG02258.hp2 others(14): Show |
intron_variant | MODIFIER | c.684+6967T>C | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 9/10 | chr11 | 43847031 | |||||||
| chr11:43847087 | TAG | T | 182 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(179): Show |
183 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(180): Show |
intron_variant | MODIFIER | c.684+7029_684+7030d others(4): Show |
HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr11 | 43847087 | ||||||
| chr11:43847101 | T | C | 182 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(179): Show |
183 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(180): Show |
intron_variant | MODIFIER | c.684+7037T>C | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 9/10 | chr11 | 43847101 | |||||||
| chr11:43847170 | G | A | 1 | a0002c0002t0002g0143 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.684+7106G>A | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 9/10 | chr11 | 43847170 | |||||||
| chr11:43847632 | A | T | 14 | a0001c0001t0003g0013 a0001c0001t0003g0014 a0001c0001t0003g0015 others(11): Show |
14 | HG00280.hp1 HG00609.hp2 NA18612.hp2 others(11): Show |
intron_variant | MODIFIER | c.685-7083A>T | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 9/10 | chr11 | 43847632 | |||||||
| chr11:43847659 | A | G | 1 | a0002c0002t0009g0200 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.685-7056A>G | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 9/10 | chr11 | 43847659 | |||||||
| chr11:43847664 | GTCACTGC others(2): Show |
G | 9 | a0001c0001t0001g0005 a0001c0001t0001g0007 a0001c0001t0001g0008 others(6): Show |
9 | HG01261.hp2 HG01884.hp2 HG02809.hp1 others(6): Show |
intron_variant | MODIFIER | c.685-7048_685-7040d others(11): Show |
HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr11 | 43847664 | ||||||
| chr11:43847715 | C | CAAA | 15 | a0001c0001t0001g0002 a0001c0001t0001g0120 a0001c0001t0001g0122 others(12): Show |
16 | HG01109.hp1 HG02258.hp2 HG02280.hp1 others(13): Show |
intron_variant | MODIFIER | c.685-6984_685-6982d others(5): Show |
HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr11 | 43847715 | ||||||
| chr11:43847715 | C | CAAAA | 74 | a0001c0001t0001g0026 a0001c0001t0001g0028 a0001c0001t0001g0029 others(71): Show |
74 | HG00099.hp1 HG00280.hp1 HG00323.hp2 others(71): Show |
intron_variant | MODIFIER | c.685-6985_685-6982d others(6): Show |
HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr11 | 43847715 | ||||||
| chr11:43847715 | C | CAAAAA | 22 | a0001c0001t0001g0034 a0001c0001t0001g0046 a0001c0001t0001g0052 others(19): Show |
22 | HG01123.hp1 HG02055.hp1 HG02055.hp2 others(19): Show |
intron_variant | MODIFIER | c.685-6986_685-6982d others(7): Show |
HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr11 | 43847715 | ||||||
| chr11:43847715 | C | CAAAAAAA others(2): Show |
37 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(34): Show |
37 | HG00099.hp2 HG00140.hp1 HG00639.hp2 others(34): Show |
intron_variant | MODIFIER | c.685-6990_685-6982d others(11): Show |
HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr11 | 43847715 | ||||||
| chr11:43847715 | C | CAAAAAAA others(3): Show |
18 | a0001c0001t0001g0129 a0001c0001t0001g0186 a0001c0001t0001g0208 others(15): Show |
18 | HG01069.hp1 HG01106.hp1 HG01891.hp2 others(15): Show |
intron_variant | MODIFIER | c.685-6991_685-6982d others(12): Show |
HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr11 | 43847715 | ||||||
| chr11:43847715 | C | CAAAAAAA others(4): Show |
9 | a0001c0001t0003g0278 a0001c0003t0001g0273 a0001c0003t0003g0242 others(6): Show |
9 | HG00642.hp2 HG01070.hp2 HG01071.hp1 others(6): Show |
intron_variant | MODIFIER | c.685-6992_685-6982d others(13): Show |
HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr11 | 43847715 | ||||||
| chr11:43847715 | C | CAAAAAAA others(5): Show |
3 | a0001c0001t0003g0267 a0001c0001t0003g0268 a0001c0001t0011g0269 |
3 | HG02572.hp1 HG03209.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.685-6993_685-6982d others(14): Show |
HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr11 | 43847715 | ||||||
| chr11:43847715 | C | CAAAAAAA others(10): Show |
2 | a0001c0003t0001g0229 a0002c0002t0008g0003 |
2 | HG02717.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.685-6998_685-6982d others(19): Show |
HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr11 | 43847715 | ||||||
| chr11:43847811 | T | C | 1 | a0002c0002t0002g0134 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.685-6904T>C | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 9/10 | chr11 | 43847811 | |||||||
| chr11:43847931 | A | G | 19 | a0001c0001t0001g0060 a0001c0001t0001g0061 a0001c0001t0001g0062 others(16): Show |
19 | HG00280.hp1 HG00609.hp2 HG02300.hp2 others(16): Show |
intron_variant | MODIFIER | c.685-6784A>G | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 9/10 | chr11 | 43847931 | |||||||
| chr11:43848120 | G | A | 1 | a0002c0002t0008g0003 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.685-6595G>A | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 9/10 | chr11 | 43848120 | |||||||
| chr11:43848273 | C | T | 93 | a0001c0001t0001g0002 a0001c0001t0001g0026 a0001c0001t0001g0028 others(90): Show |
94 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(91): Show |
intron_variant | MODIFIER | c.685-6442C>T | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 9/10 | chr11 | 43848273 | |||||||
| chr11:43848295 | G | A | 1 | a0001c0003t0001g0238 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.685-6420G>A | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 9/10 | chr11 | 43848295 | |||||||
| chr11:43848310 | C | G | 220 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(217): Show |
221 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(218): Show |
intron_variant | MODIFIER | c.685-6405C>G | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 9/10 | chr11 | 43848310 | |||||||
| chr11:43848354 | C | T | 7 | a0001c0003t0003g0242 a0001c0003t0003g0243 a0001c0003t0003g0244 others(4): Show |
7 | HG01070.hp2 HG01071.hp1 HG02004.hp1 others(4): Show |
intron_variant | MODIFIER | c.685-6361C>T | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 9/10 | chr11 | 43848354 | |||||||
| chr11:43848389 | G | A | 163 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(160): Show |
164 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(161): Show |
intron_variant | MODIFIER | c.685-6326G>A | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 9/10 | chr11 | 43848389 | |||||||
| chr11:43848430 | C | T | 163 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(160): Show |
164 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(161): Show |
intron_variant | MODIFIER | c.685-6285C>T | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 9/10 | chr11 | 43848430 | |||||||
| chr11:43848673 | G | A | 2 | a0001c0001t0001g0034 a0001c0001t0001g0071 |
2 | NA18945.hp2 NA18982.hp1 |
intron_variant | MODIFIER | c.685-6042G>A | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 9/10 | chr11 | 43848673 | |||||||
| chr11:43849321 | C | CA | 54 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(51): Show |
54 | HG00099.hp2 HG00140.hp1 HG00639.hp2 others(51): Show |
intron_variant | MODIFIER | c.685-5387dupA | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr11 | 43849321 | ||||||
| chr11:43849325 | A | AC | 3 | a0003c0004t0001g0241 a0003c0004t0001g0249 a0003c0004t0001g0264 |
3 | HG02647.hp2 HG03516.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.685-5390_685-5389i others(3): Show |
HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 9/10 | chr11 | 43849325 | |||||||
| chr11:43849629 | C | A | 1 | a0001c0001t0001g0042 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.685-5086C>A | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 9/10 | chr11 | 43849629 | |||||||
| chr11:43849662 | C | G | 163 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(160): Show |
164 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(161): Show |
intron_variant | MODIFIER | c.685-5053C>G | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 9/10 | chr11 | 43849662 | |||||||
| chr11:43849805 | T | C | 14 | a0001c0001t0003g0013 a0001c0001t0003g0014 a0001c0001t0003g0015 others(11): Show |
14 | HG00280.hp1 HG00609.hp2 NA18612.hp2 others(11): Show |
intron_variant | MODIFIER | c.685-4910T>C | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 9/10 | chr11 | 43849805 | |||||||
| chr11:43849975 | G | A | 1 | a0001c0001t0003g0206 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.685-4740G>A | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 9/10 | chr11 | 43849975 | |||||||
| chr11:43850032 | C | A | 1 | a0002c0002t0002g0154 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.685-4683C>A | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 9/10 | chr11 | 43850032 | |||||||
| chr11:43850128 | C | T | 1 | a0002c0002t0008g0003 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.685-4587C>T | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 9/10 | chr11 | 43850128 | |||||||
| chr11:43850247 | G | A | 182 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(179): Show |
183 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(180): Show |
intron_variant | MODIFIER | c.685-4468G>A | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 9/10 | chr11 | 43850247 | |||||||
| chr11:43850446 | A | C | 182 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(179): Show |
183 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(180): Show |
intron_variant | MODIFIER | c.685-4269A>C | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 9/10 | chr11 | 43850446 | |||||||
| chr11:43850905 | T | C | 163 | a0001c0001t0001g0002 a0001c0001t0001g0005 a0001c0001t0001g0006 others(160): Show |
164 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(161): Show |
intron_variant | MODIFIER | c.685-3810T>C | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 9/10 | chr11 | 43850905 | |||||||
| chr11:43850934 | G | A | 4 | a0001c0001t0001g0111 a0001c0001t0001g0112 a0001c0001t0001g0203 others(1): Show |
4 | HG02055.hp1 HG02809.hp2 HG02895.hp1 others(1): Show |
intron_variant | MODIFIER | c.685-3781G>A | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 9/10 | chr11 | 43850934 | |||||||
| chr11:43850967 | A | C | 1 | a0001c0001t0003g0206 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.685-3748A>C | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 9/10 | chr11 | 43850967 | |||||||
| chr11:43851356 | T | C | 1 | a0001c0001t0001g0260 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.685-3359T>C | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 9/10 | chr11 | 43851356 | |||||||
| chr11:43851394 | C | A | 93 | a0001c0001t0001g0002 a0001c0001t0001g0026 a0001c0001t0001g0028 others(90): Show |
94 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(91): Show |
intron_variant | MODIFIER | c.685-3321C>A | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 9/10 | chr11 | 43851394 | |||||||
| chr11:43851456 | T | C | 2 | a0002c0002t0002g0150 a0002c0002t0002g0160 |
2 | HG00609.hp1 HG02155.hp2 |
intron_variant | MODIFIER | c.685-3259T>C | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 9/10 | chr11 | 43851456 | |||||||
| chr11:43851798 | G | A | 1 | a0001c0001t0003g0023 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.685-2917G>A | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 9/10 | chr11 | 43851798 | |||||||
| chr11:43851828 | T | C | 1 | a0002c0002t0008g0003 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.685-2887T>C | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 9/10 | chr11 | 43851828 | |||||||
| chr11:43851989 | C | A | 38 | a0002c0002t0002g0004 a0002c0002t0002g0027 a0002c0002t0002g0109 others(35): Show |
38 | HG00280.hp2 HG00423.hp1 HG00738.hp1 others(35): Show |
intron_variant | MODIFIER | c.685-2726C>A | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 9/10 | chr11 | 43851989 | |||||||
| chr11:43852064 | C | A | 3 | a0001c0001t0001g0029 a0001c0001t0001g0035 a0001c0001t0001g0048 |
3 | HG02135.hp2 NA19070.hp2 NA19090.hp2 |
intron_variant | MODIFIER | c.685-2651C>A | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 9/10 | chr11 | 43852064 | |||||||
| chr11:43852085 | T | C | 12 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(9): Show |
12 | HG01261.hp2 HG01884.hp2 HG02257.hp1 others(9): Show |
intron_variant | MODIFIER | c.685-2630T>C | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 9/10 | chr11 | 43852085 | |||||||
| chr11:43852184 | C | T | 19 | a0001c0001t0001g0060 a0001c0001t0001g0061 a0001c0001t0001g0062 others(16): Show |
19 | HG00280.hp1 HG00609.hp2 HG02300.hp2 others(16): Show |
intron_variant | MODIFIER | c.685-2531C>T | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 9/10 | chr11 | 43852184 | |||||||
| chr11:43852189 | G | A | 1 | a0002c0002t0008g0003 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.685-2526G>A | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 9/10 | chr11 | 43852189 | |||||||
| chr11:43852274 | A | G | 3 | a0003c0004t0001g0241 a0003c0004t0001g0249 a0003c0004t0001g0264 |
3 | HG02647.hp2 HG03516.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.685-2441A>G | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 9/10 | chr11 | 43852274 | |||||||
| chr11:43852353 | A | G | 1 | a0001c0001t0003g0206 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.685-2362A>G | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 9/10 | chr11 | 43852353 | |||||||
| chr11:43852369 | G | A | 1 | a0001c0001t0001g0254 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.685-2346G>A | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 9/10 | chr11 | 43852369 | |||||||
| chr11:43852459 | G | GT | 37 | a0001c0001t0001g0002 a0001c0001t0001g0050 a0001c0001t0001g0111 others(34): Show |
38 | HG00280.hp1 HG00609.hp2 HG01109.hp1 others(35): Show |
intron_variant | MODIFIER | c.685-2245dupT | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr11 | 43852459 | ||||||
| chr11:43852459 | G | GTT | 71 | a0001c0001t0001g0026 a0001c0001t0001g0028 a0001c0001t0001g0029 others(68): Show |
71 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(68): Show |
intron_variant | MODIFIER | c.685-2246_685-2245d others(4): Show |
HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr11 | 43852459 | ||||||
| chr11:43852500 | T | C | 4 | a0001c0001t0003g0267 a0001c0001t0003g0268 a0001c0001t0003g0278 others(1): Show |
4 | HG02572.hp1 HG02965.hp2 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.685-2215T>C | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 9/10 | chr11 | 43852500 | |||||||
| chr11:43852516 | G | T | 1 | a0001c0007t0001g0230 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.685-2199G>T | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 9/10 | chr11 | 43852516 | |||||||
| chr11:43852674 | C | T | 4 | a0002c0002t0002g0165 a0002c0002t0002g0180 a0004c0005t0002g0011 others(1): Show |
4 | HG00323.hp1 HG01099.hp2 HG01106.hp2 others(1): Show |
intron_variant | MODIFIER | c.685-2041C>T | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 9/10 | chr11 | 43852674 | |||||||
| chr11:43852731 | C | A | 7 | a0001c0001t0001g0209 a0001c0001t0001g0210 a0001c0001t0001g0211 others(4): Show |
7 | HG01928.hp2 HG02523.hp2 NA18966.hp2 others(4): Show |
intron_variant | MODIFIER | c.685-1984C>A | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 9/10 | chr11 | 43852731 | |||||||
| chr11:43852751 | A | T | 3 | a0001c0001t0001g0029 a0001c0001t0001g0035 a0001c0001t0001g0048 |
3 | HG02135.hp2 NA19070.hp2 NA19090.hp2 |
intron_variant | MODIFIER | c.685-1964A>T | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 9/10 | chr11 | 43852751 | |||||||
| chr11:43853123 | G | C | 2 | a0002c0002t0004g0205 a0002c0002t0004g0274 |
2 | HG02451.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.685-1592G>C | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 9/10 | chr11 | 43853123 | |||||||
| chr11:43853178 | A | T | 1 | a0002c0002t0002g0252 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.685-1537A>T | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 9/10 | chr11 | 43853178 | |||||||
| chr11:43853329 | C | T | 28 | a0001c0001t0003g0013 a0001c0001t0003g0014 a0001c0001t0003g0015 others(25): Show |
28 | HG00280.hp1 HG00609.hp2 HG01070.hp2 others(25): Show |
intron_variant | MODIFIER | c.685-1386C>T | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 9/10 | chr11 | 43853329 | |||||||
| chr11:43853337 | C | CA | 62 | a0001c0001t0001g0010 a0001c0001t0001g0028 a0001c0001t0001g0030 others(59): Show |
62 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(59): Show |
intron_variant | MODIFIER | c.685-1351dupA | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr11 | 43853337 | ||||||
| chr11:43853337 | C | CAA | 25 | a0001c0001t0001g0026 a0001c0001t0001g0029 a0001c0001t0001g0036 others(22): Show |
25 | HG00738.hp2 HG01175.hp1 HG01192.hp1 others(22): Show |
intron_variant | MODIFIER | c.685-1352_685-1351d others(4): Show |
HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr11 | 43853337 | ||||||
| chr11:43853337 | CA | C | 16 | a0001c0001t0001g0128 a0001c0001t0001g0129 a0001c0001t0001g0262 others(13): Show |
16 | HG00639.hp2 HG00642.hp2 HG01069.hp1 others(13): Show |
intron_variant | MODIFIER | c.685-1351delA | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr11 | 43853337 | ||||||
| chr11:43853337 | CAAAAAAA others(2): Show |
C | 92 | a0002c0002t0002g0001 a0002c0002t0002g0004 a0002c0002t0002g0025 others(89): Show |
93 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(90): Show |
intron_variant | MODIFIER | c.685-1359_685-1351d others(11): Show |
HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr11 | 43853337 | ||||||
| chr11:43853337 | CAAAAAAA others(3): Show |
C | 2 | a0001c0007t0001g0230 a0002c0002t0009g0200 |
2 | HG02258.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.685-1360_685-1351d others(12): Show |
HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr11 | 43853337 | ||||||
| chr11:43853337 | CAAAAAAA others(6): Show |
C | 28 | a0001c0001t0003g0013 a0001c0001t0003g0014 a0001c0001t0003g0015 others(25): Show |
28 | HG00280.hp1 HG00609.hp2 HG01070.hp2 others(25): Show |
intron_variant | MODIFIER | c.685-1363_685-1351d others(15): Show |
HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr11 | 43853337 | ||||||
| chr11:43853404 | C | T | 1 | a0001c0001t0003g0019 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.685-1311C>T | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 9/10 | chr11 | 43853404 | |||||||
| chr11:43853633 | T | A | 1 | a0001c0001t0003g0206 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.685-1082T>A | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 9/10 | chr11 | 43853633 | |||||||
| chr11:43853762 | C | G | 14 | a0001c0001t0003g0013 a0001c0001t0003g0014 a0001c0001t0003g0015 others(11): Show |
14 | HG00280.hp1 HG00609.hp2 NA18612.hp2 others(11): Show |
intron_variant | MODIFIER | c.685-953C>G | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 9/10 | chr11 | 43853762 | |||||||
| chr11:43853766 | G | A | 98 | a0002c0002t0002g0001 a0002c0002t0002g0004 a0002c0002t0002g0025 others(95): Show |
99 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(96): Show |
intron_variant | MODIFIER | c.685-949G>A | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 9/10 | chr11 | 43853766 | |||||||
| chr11:43853819 | TATC | T | 98 | a0002c0002t0002g0001 a0002c0002t0002g0004 a0002c0002t0002g0025 others(95): Show |
99 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(96): Show |
intron_variant | MODIFIER | c.685-893_685-891del others(3): Show |
HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr11 | 43853819 | ||||||
| chr11:43854024 | G | C | 2 | a0002c0002t0004g0205 a0002c0002t0004g0274 |
2 | HG02451.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.685-691G>C | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 9/10 | chr11 | 43854024 | |||||||
| chr11:43854145 | G | A | 4 | a0002c0002t0002g0117 a0002c0002t0002g0118 a0002c0002t0002g0119 others(1): Show |
4 | HG00408.hp2 HG02135.hp1 NA19084.hp2 others(1): Show |
intron_variant | MODIFIER | c.685-570G>A | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 9/10 | chr11 | 43854145 | |||||||
| chr11:43854164 | T | C | 98 | a0002c0002t0002g0001 a0002c0002t0002g0004 a0002c0002t0002g0025 others(95): Show |
99 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(96): Show |
intron_variant | MODIFIER | c.685-551T>C | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 9/10 | chr11 | 43854164 | |||||||
| chr11:43854224 | C | T | 2 | a0002c0002t0002g0190 a0002c0002t0002g0191 |
2 | NA18982.hp2 NA19060.hp1 |
intron_variant | MODIFIER | c.685-491C>T | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 9/10 | chr11 | 43854224 | |||||||
| chr11:43854464 | A | G | 1 | a0001c0007t0001g0230 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.685-251A>G | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 9/10 | chr11 | 43854464 | |||||||
| chr11:43854532 | A | G | 1 | a0001c0001t0001g0257 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.685-183A>G | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 9/10 | chr11 | 43854532 | |||||||
| chr11:43854586 | C | G | 1 | a0001c0007t0001g0230 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.685-129C>G | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 9/10 | chr11 | 43854586 | |||||||
| chr11:43854885 | A | G | 99 | a0001c0007t0001g0230 a0002c0002t0002g0001 a0002c0002t0002g0004 others(96): Show |
100 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(97): Show |
intron_variant | MODIFIER | c.834+21A>G | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 10/10 | chr11 | 43854885 | |||||||
| chr11:43854990 | A | G | 28 | a0001c0001t0003g0013 a0001c0001t0003g0014 a0001c0001t0003g0015 others(25): Show |
28 | HG00280.hp1 HG00609.hp2 HG01070.hp2 others(25): Show |
intron_variant | MODIFIER | c.834+126A>G | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 10/10 | chr11 | 43854990 | |||||||
| chr11:43855059 | C | T | 1 | a0001c0001t0003g0206 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.835-85C>T | HSD17B12 | ENSG00000149084.13 | transcript | ENST00000278353.10 | protein_coding | 10/10 | chr11 | 43855059 |