Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 79157 |
| ensemblid | ENSG00000092931.12 |
| hgncid | 25458 |
| symbol | MFSD11 |
| name | major facilitator superfamily domain containing 11 |
| refseq_nuc | NM_001242532.5 |
| refseq_prot | NP_001229461.1 |
| ensembl_nuc | ENST00000685175.1 |
| ensembl_prot | ENSP00000508960.1 |
| mane_status | MANE Select |
| chr | chr17 |
| start | 76738119 |
| end | 76779341 |
| strand | + |
| ver | v1.2 |
| region | chr17:76738119-76779341 |
| region5000 | chr17:76733119-76784341 |
| regionname0 | MFSD11_chr17_76738119_76779341 |
| regionname5000 | MFSD11_chr17_76733119_76784341 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 449 | 345 | 85 | 58 | 155 | 14 | 31 | 115 | MFSD11_chr17_76733119_76784341 | MFSD11 | MSPES others(444): Show |
chr17 | 76733119 | 76784341 |
| a0002 | 0/0 | 449 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | MFSD11_chr17_76733119_76784341 | MFSD11 | MSPES others(444): Show |
chr17 | 76733119 | 76784341 |
| a0003 | 0/0 | 449 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | MFSD11_chr17_76733119_76784341 | MFSD11 | MSPES others(444): Show |
chr17 | 76733119 | 76784341 |
| a0004 | 0/0 | 449 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | MFSD11_chr17_76733119_76784341 | MFSD11 | MSPES others(444): Show |
chr17 | 76733119 | 76784341 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 1347 | 330 | 76 | 57 | 153 | 14 | 28 | MFSD11_chr17_76733119_76784341 | MFSD11 | ATGTC others(1342): Show |
chr17 | 76733119 | 76784341 | ||
| a0001c0002 | 0/0 | 1347 | 5 | 4 | 1 | 0 | 0 | 0 | MFSD11_chr17_76733119_76784341 | MFSD11 | ATGTC others(1342): Show |
chr17 | 76733119 | 76784341 | ||
| a0001c0003 | 0/0 | 1347 | 3 | 3 | 0 | 0 | 0 | 0 | MFSD11_chr17_76733119_76784341 | MFSD11 | ATGTC others(1342): Show |
chr17 | 76733119 | 76784341 | ||
| a0001c0004 | 0/0 | 1347 | 2 | 2 | 0 | 0 | 0 | 0 | MFSD11_chr17_76733119_76784341 | MFSD11 | ATGTC others(1342): Show |
chr17 | 76733119 | 76784341 | ||
| a0001c0005 | 0/0 | 1347 | 2 | 0 | 0 | 2 | 0 | 0 | MFSD11_chr17_76733119_76784341 | MFSD11 | ATGTC others(1342): Show |
chr17 | 76733119 | 76784341 | ||
| a0001c0006 | 0/0 | 1347 | 2 | 0 | 0 | 0 | 0 | 2 | MFSD11_chr17_76733119_76784341 | MFSD11 | ATGTC others(1342): Show |
chr17 | 76733119 | 76784341 | ||
| a0001c0008 | 0/0 | 1347 | 1 | 0 | 0 | 0 | 0 | 1 | MFSD11_chr17_76733119_76784341 | MFSD11 | ATGTC others(1342): Show |
chr17 | 76733119 | 76784341 | ||
| a0002c0007 | 0/0 | 1347 | 1 | 1 | 0 | 0 | 0 | 0 | MFSD11_chr17_76733119_76784341 | MFSD11 | ATGTC others(1342): Show |
chr17 | 76733119 | 76784341 | ||
| a0003c0009 | 0/0 | 1347 | 1 | 0 | 0 | 0 | 0 | 1 | MFSD11_chr17_76733119_76784341 | MFSD11 | ATGTC others(1342): Show |
chr17 | 76733119 | 76784341 | ||
| a0004c0010 | 0/0 | 1347 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD11_chr17_76733119_76784341 | MFSD11 | ATGTC others(1342): Show |
chr17 | 76733119 | 76784341 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/1 | 2573 | 176 | 49 | 39 | 62 | 11 | 14 | MFSD11_chr17_76733119_76784341 | MFSD11 | GTGCT others(2568): Show |
chr17 | 76733119 | 76784341 |
| a0001c0001t0002 | 0/0 | 2573 | 116 | 0 | 13 | 87 | 3 | 13 | MFSD11_chr17_76733119_76784341 | MFSD11 | GTGCT others(2568): Show |
chr17 | 76733119 | 76784341 |
| a0001c0001t0003 | 0/0 | 2573 | 19 | 14 | 1 | 4 | 0 | 0 | MFSD11_chr17_76733119_76784341 | MFSD11 | GTGCT others(2568): Show |
chr17 | 76733119 | 76784341 |
| a0001c0001t0004 | 0/0 | 2573 | 6 | 5 | 1 | 0 | 0 | 0 | MFSD11_chr17_76733119_76784341 | MFSD11 | GTGCT others(2568): Show |
chr17 | 76733119 | 76784341 |
| a0001c0001t0005 | 0/0 | 2573 | 5 | 5 | 0 | 0 | 0 | 0 | MFSD11_chr17_76733119_76784341 | MFSD11 | GTGCT others(2568): Show |
chr17 | 76733119 | 76784341 |
| a0001c0001t0006 | 0/0 | 2573 | 2 | 1 | 1 | 0 | 0 | 0 | MFSD11_chr17_76733119_76784341 | MFSD11 | GTGCT others(2568): Show |
chr17 | 76733119 | 76784341 |
| a0001c0001t0008 | 0/0 | 2573 | 1 | 1 | 0 | 0 | 0 | 0 | MFSD11_chr17_76733119_76784341 | MFSD11 | GTGCT others(2568): Show |
chr17 | 76733119 | 76784341 |
| a0001c0001t0009 | 0/0 | 2573 | 1 | 0 | 1 | 0 | 0 | 0 | MFSD11_chr17_76733119_76784341 | MFSD11 | GTGCT others(2568): Show |
chr17 | 76733119 | 76784341 |
| a0001c0001t0010 | 0/0 | 2573 | 1 | 0 | 1 | 0 | 0 | 0 | MFSD11_chr17_76733119_76784341 | MFSD11 | GTGCT others(2568): Show |
chr17 | 76733119 | 76784341 |
| a0001c0001t0011 | 0/0 | 2573 | 1 | 0 | 0 | 0 | 0 | 1 | MFSD11_chr17_76733119_76784341 | MFSD11 | GTGCT others(2568): Show |
chr17 | 76733119 | 76784341 |
| a0001c0001t0013 | 0/0 | 2573 | 1 | 1 | 0 | 0 | 0 | 0 | MFSD11_chr17_76733119_76784341 | MFSD11 | GTGCT others(2568): Show |
chr17 | 76733119 | 76784341 |
| a0001c0001t0014 | 1/0 | 2573 | 1 | 0 | 0 | 0 | 0 | 0 | MFSD11_chr17_76733119_76784341 | MFSD11 | GTGCT others(2568): Show |
chr17 | 76733119 | 76784341 |
| a0001c0002t0001 | 0/0 | 2573 | 5 | 4 | 1 | 0 | 0 | 0 | MFSD11_chr17_76733119_76784341 | MFSD11 | GTGCT others(2568): Show |
chr17 | 76733119 | 76784341 |
| a0001c0003t0002 | 0/0 | 2573 | 3 | 3 | 0 | 0 | 0 | 0 | MFSD11_chr17_76733119_76784341 | MFSD11 | GTGCT others(2568): Show |
chr17 | 76733119 | 76784341 |
| a0001c0004t0001 | 0/0 | 2573 | 2 | 2 | 0 | 0 | 0 | 0 | MFSD11_chr17_76733119_76784341 | MFSD11 | GTGCT others(2568): Show |
chr17 | 76733119 | 76784341 |
| a0001c0005t0001 | 0/0 | 2573 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD11_chr17_76733119_76784341 | MFSD11 | GTGCT others(2568): Show |
chr17 | 76733119 | 76784341 |
| a0001c0005t0012 | 0/0 | 2573 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD11_chr17_76733119_76784341 | MFSD11 | GTGCT others(2568): Show |
chr17 | 76733119 | 76784341 |
| a0001c0006t0007 | 0/0 | 2573 | 2 | 0 | 0 | 0 | 0 | 2 | MFSD11_chr17_76733119_76784341 | MFSD11 | GTGCT others(2568): Show |
chr17 | 76733119 | 76784341 |
| a0001c0008t0001 | 0/0 | 2573 | 1 | 0 | 0 | 0 | 0 | 1 | MFSD11_chr17_76733119_76784341 | MFSD11 | GTGCT others(2568): Show |
chr17 | 76733119 | 76784341 |
| a0002c0007t0001 | 0/0 | 2573 | 1 | 1 | 0 | 0 | 0 | 0 | MFSD11_chr17_76733119_76784341 | MFSD11 | GTGCT others(2568): Show |
chr17 | 76733119 | 76784341 |
| a0003c0009t0001 | 0/0 | 2573 | 1 | 0 | 0 | 0 | 0 | 1 | MFSD11_chr17_76733119_76784341 | MFSD11 | GTGCT others(2568): Show |
chr17 | 76733119 | 76784341 |
| a0004c0010t0001 | 0/0 | 2573 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD11_chr17_76733119_76784341 | MFSD11 | GTGCT others(2568): Show |
chr17 | 76733119 | 76784341 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0003 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | MFSD11_chr17_76733119_76784341 | MFSD11 | chr17 | 76733119 | 76784341 |
| a0001c0001t0001g0007 | 0/0 | 2 | 1 | 0 | 0 | 0 | 1 | MFSD11_chr17_76733119_76784341 | MFSD11 | chr17 | 76733119 | 76784341 |
| a0001c0001t0001g0010 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MFSD11_chr17_76733119_76784341 | MFSD11 | chr17 | 76733119 | 76784341 |
| a0001c0001t0001g0044 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MFSD11_chr17_76733119_76784341 | MFSD11 | chr17 | 76733119 | 76784341 |
| a0001c0001t0001g0045 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | MFSD11_chr17_76733119_76784341 | MFSD11 | chr17 | 76733119 | 76784341 |
| a0001c0001t0001g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD11_chr17_76733119_76784341 | MFSD11 | chr17 | 76733119 | 76784341 |
| a0001c0001t0001g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD11_chr17_76733119_76784341 | MFSD11 | chr17 | 76733119 | 76784341 |
| a0001c0001t0001g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD11_chr17_76733119_76784341 | MFSD11 | chr17 | 76733119 | 76784341 |
| a0001c0001t0001g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD11_chr17_76733119_76784341 | MFSD11 | chr17 | 76733119 | 76784341 |
| a0001c0001t0001g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD11_chr17_76733119_76784341 | MFSD11 | chr17 | 76733119 | 76784341 |
| a0001c0001t0001g0052 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MFSD11_chr17_76733119_76784341 | MFSD11 | chr17 | 76733119 | 76784341 |
| a0001c0001t0001g0053 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MFSD11_chr17_76733119_76784341 | MFSD11 | chr17 | 76733119 | 76784341 |
| a0001c0001t0001g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD11_chr17_76733119_76784341 | MFSD11 | chr17 | 76733119 | 76784341 |
| a0001c0001t0001g0055 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MFSD11_chr17_76733119_76784341 | MFSD11 | chr17 | 76733119 | 76784341 |
| a0001c0001t0001g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD11_chr17_76733119_76784341 | MFSD11 | chr17 | 76733119 | 76784341 |
| a0001c0001t0001g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD11_chr17_76733119_76784341 | MFSD11 | chr17 | 76733119 | 76784341 |
| a0001c0001t0001g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD11_chr17_76733119_76784341 | MFSD11 | chr17 | 76733119 | 76784341 |
| a0001c0001t0001g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD11_chr17_76733119_76784341 | MFSD11 | chr17 | 76733119 | 76784341 |
| a0001c0001t0001g0065 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MFSD11_chr17_76733119_76784341 | MFSD11 | chr17 | 76733119 | 76784341 |
| a0001c0001t0001g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD11_chr17_76733119_76784341 | MFSD11 | chr17 | 76733119 | 76784341 |
| a0001c0001t0001g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD11_chr17_76733119_76784341 | MFSD11 | chr17 | 76733119 | 76784341 |
| a0001c0001t0001g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD11_chr17_76733119_76784341 | MFSD11 | chr17 | 76733119 | 76784341 |
| a0001c0001t0001g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFSD11_chr17_76733119_76784341 | MFSD11 | chr17 | 76733119 | 76784341 |
| a0001c0001t0001g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD11_chr17_76733119_76784341 | MFSD11 | chr17 | 76733119 | 76784341 |
| a0001c0001t0001g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD11_chr17_76733119_76784341 | MFSD11 | chr17 | 76733119 | 76784341 |
| a0001c0001t0001g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFSD11_chr17_76733119_76784341 | MFSD11 | chr17 | 76733119 | 76784341 |
| a0001c0001t0001g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFSD11_chr17_76733119_76784341 | MFSD11 | chr17 | 76733119 | 76784341 |
| a0001c0001t0001g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFSD11_chr17_76733119_76784341 | MFSD11 | chr17 | 76733119 | 76784341 |
| a0001c0001t0001g0087 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MFSD11_chr17_76733119_76784341 | MFSD11 | chr17 | 76733119 | 76784341 |
| a0001c0001t0001g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFSD11_chr17_76733119_76784341 | MFSD11 | chr17 | 76733119 | 76784341 |
| a0001c0001t0001g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MFSD11_chr17_76733119_76784341 | MFSD11 | chr17 | 76733119 | 76784341 |
| a0001c0001t0001g0098 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MFSD11_chr17_76733119_76784341 | MFSD11 | chr17 | 76733119 | 76784341 |
| a0001c0001t0001g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFSD11_chr17_76733119_76784341 | MFSD11 | chr17 | 76733119 | 76784341 |
| a0001c0001t0001g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD11_chr17_76733119_76784341 | MFSD11 | chr17 | 76733119 | 76784341 |
| a0001c0001t0001g0103 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MFSD11_chr17_76733119_76784341 | MFSD11 | chr17 | 76733119 | 76784341 |
| a0001c0001t0001g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFSD11_chr17_76733119_76784341 | MFSD11 | chr17 | 76733119 | 76784341 |
| a0001c0001t0001g0116 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MFSD11_chr17_76733119_76784341 | MFSD11 | chr17 | 76733119 | 76784341 |
| a0001c0001t0001g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD11_chr17_76733119_76784341 | MFSD11 | chr17 | 76733119 | 76784341 |
| a0001c0001t0001g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD11_chr17_76733119_76784341 | MFSD11 | chr17 | 76733119 | 76784341 |
| a0001c0001t0001g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFSD11_chr17_76733119_76784341 | MFSD11 | chr17 | 76733119 | 76784341 |
| a0001c0001t0001g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFSD11_chr17_76733119_76784341 | MFSD11 | chr17 | 76733119 | 76784341 |
| a0001c0001t0001g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD11_chr17_76733119_76784341 | MFSD11 | chr17 | 76733119 | 76784341 |
| a0001c0001t0001g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD11_chr17_76733119_76784341 | MFSD11 | chr17 | 76733119 | 76784341 |
| a0001c0001t0001g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFSD11_chr17_76733119_76784341 | MFSD11 | chr17 | 76733119 | 76784341 |
| a0001c0001t0001g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFSD11_chr17_76733119_76784341 | MFSD11 | chr17 | 76733119 | 76784341 |
| a0001c0001t0001g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFSD11_chr17_76733119_76784341 | MFSD11 | chr17 | 76733119 | 76784341 |
| a0001c0001t0001g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD11_chr17_76733119_76784341 | MFSD11 | chr17 | 76733119 | 76784341 |
| a0001c0001t0001g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD11_chr17_76733119_76784341 | MFSD11 | chr17 | 76733119 | 76784341 |
| a0001c0001t0001g0140 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MFSD11_chr17_76733119_76784341 | MFSD11 | chr17 | 76733119 | 76784341 |
| a0001c0001t0001g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD11_chr17_76733119_76784341 | MFSD11 | chr17 | 76733119 | 76784341 |
| a0001c0001t0001g0142 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MFSD11_chr17_76733119_76784341 | MFSD11 | chr17 | 76733119 | 76784341 |
| a0001c0001t0001g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD11_chr17_76733119_76784341 | MFSD11 | chr17 | 76733119 | 76784341 |
| a0001c0001t0001g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFSD11_chr17_76733119_76784341 | MFSD11 | chr17 | 76733119 | 76784341 |
| a0001c0001t0001g0146 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MFSD11_chr17_76733119_76784341 | MFSD11 | chr17 | 76733119 | 76784341 |
| a0001c0001t0001g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFSD11_chr17_76733119_76784341 | MFSD11 | chr17 | 76733119 | 76784341 |
| a0001c0001t0001g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFSD11_chr17_76733119_76784341 | MFSD11 | chr17 | 76733119 | 76784341 |
| a0001c0001t0001g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFSD11_chr17_76733119_76784341 | MFSD11 | chr17 | 76733119 | 76784341 |
| a0001c0001t0001g0150 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MFSD11_chr17_76733119_76784341 | MFSD11 | chr17 | 76733119 | 76784341 |
| a0001c0001t0001g0151 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MFSD11_chr17_76733119_76784341 | MFSD11 | chr17 | 76733119 | 76784341 |
| a0001c0001t0001g0152 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MFSD11_chr17_76733119_76784341 | MFSD11 | chr17 | 76733119 | 76784341 |
| a0001c0001t0001g0153 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MFSD11_chr17_76733119_76784341 | MFSD11 | chr17 | 76733119 | 76784341 |
| a0001c0001t0001g0154 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MFSD11_chr17_76733119_76784341 | MFSD11 | chr17 | 76733119 | 76784341 |
| a0001c0001t0001g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD11_chr17_76733119_76784341 | MFSD11 | chr17 | 76733119 | 76784341 |
| a0001c0001t0001g0156 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MFSD11_chr17_76733119_76784341 | MFSD11 | chr17 | 76733119 | 76784341 |
| a0001c0001t0001g0157 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MFSD11_chr17_76733119_76784341 | MFSD11 | chr17 | 76733119 | 76784341 |
| a0001c0001t0001g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD11_chr17_76733119_76784341 | MFSD11 | chr17 | 76733119 | 76784341 |
| a0001c0001t0001g0160 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MFSD11_chr17_76733119_76784341 | MFSD11 | chr17 | 76733119 | 76784341 |
| a0001c0001t0001g0161 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MFSD11_chr17_76733119_76784341 | MFSD11 | chr17 | 76733119 | 76784341 |
| a0001c0001t0001g0162 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MFSD11_chr17_76733119_76784341 | MFSD11 | chr17 | 76733119 | 76784341 |
| a0001c0001t0001g0164 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MFSD11_chr17_76733119_76784341 | MFSD11 | chr17 | 76733119 | 76784341 |
| a0001c0001t0001g0167 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MFSD11_chr17_76733119_76784341 | MFSD11 | chr17 | 76733119 | 76784341 |
| a0001c0001t0001g0168 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MFSD11_chr17_76733119_76784341 | MFSD11 | chr17 | 76733119 | 76784341 |
| a0001c0001t0001g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD11_chr17_76733119_76784341 | MFSD11 | chr17 | 76733119 | 76784341 |
| a0001c0001t0001g0171 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MFSD11_chr17_76733119_76784341 | MFSD11 | chr17 | 76733119 | 76784341 |
| a0001c0001t0001g0174 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MFSD11_chr17_76733119_76784341 | MFSD11 | chr17 | 76733119 | 76784341 |
| a0001c0001t0001g0175 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MFSD11_chr17_76733119_76784341 | MFSD11 | chr17 | 76733119 | 76784341 |
| a0001c0001t0001g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFSD11_chr17_76733119_76784341 | MFSD11 | chr17 | 76733119 | 76784341 |
| a0001c0001t0001g0177 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MFSD11_chr17_76733119_76784341 | MFSD11 | chr17 | 76733119 | 76784341 |
| a0001c0001t0001g0178 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MFSD11_chr17_76733119_76784341 | MFSD11 | chr17 | 76733119 | 76784341 |
| a0001c0001t0001g0179 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MFSD11_chr17_76733119_76784341 | MFSD11 | chr17 | 76733119 | 76784341 |
| a0001c0001t0001g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD11_chr17_76733119_76784341 | MFSD11 | chr17 | 76733119 | 76784341 |
| a0001c0001t0001g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD11_chr17_76733119_76784341 | MFSD11 | chr17 | 76733119 | 76784341 |
| a0001c0001t0001g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD11_chr17_76733119_76784341 | MFSD11 | chr17 | 76733119 | 76784341 |
| a0001c0001t0001g0196 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MFSD11_chr17_76733119_76784341 | MFSD11 | chr17 | 76733119 | 76784341 |
| a0001c0001t0001g0200 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MFSD11_chr17_76733119_76784341 | MFSD11 | chr17 | 76733119 | 76784341 |
| a0001c0001t0001g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD11_chr17_76733119_76784341 | MFSD11 | chr17 | 76733119 | 76784341 |
| a0001c0001t0001g0216 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MFSD11_chr17_76733119_76784341 | MFSD11 | chr17 | 76733119 | 76784341 |
| a0001c0001t0001g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD11_chr17_76733119_76784341 | MFSD11 | chr17 | 76733119 | 76784341 |
| a0001c0001t0001g0224 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MFSD11_chr17_76733119_76784341 | MFSD11 | chr17 | 76733119 | 76784341 |
| a0001c0001t0001g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFSD11_chr17_76733119_76784341 | MFSD11 | chr17 | 76733119 | 76784341 |
| a0001c0001t0001g0226 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MFSD11_chr17_76733119_76784341 | MFSD11 | chr17 | 76733119 | 76784341 |
| a0001c0001t0001g0227 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MFSD11_chr17_76733119_76784341 | MFSD11 | chr17 | 76733119 | 76784341 |
| a0001c0001t0001g0228 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MFSD11_chr17_76733119_76784341 | MFSD11 | chr17 | 76733119 | 76784341 |
| a0001c0001t0001g0230 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MFSD11_chr17_76733119_76784341 | MFSD11 | chr17 | 76733119 | 76784341 |
| a0001c0001t0001g0231 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MFSD11_chr17_76733119_76784341 | MFSD11 | chr17 | 76733119 | 76784341 |
| a0001c0001t0001g0232 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MFSD11_chr17_76733119_76784341 | MFSD11 | chr17 | 76733119 | 76784341 |
| a0001c0001t0001g0233 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MFSD11_chr17_76733119_76784341 | MFSD11 | chr17 | 76733119 | 76784341 |
| a0001c0001t0001g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFSD11_chr17_76733119_76784341 | MFSD11 | chr17 | 76733119 | 76784341 |
| a0001c0001t0001g0235 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MFSD11_chr17_76733119_76784341 | MFSD11 | chr17 | 76733119 | 76784341 |
| a0001c0001t0001g0236 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MFSD11_chr17_76733119_76784341 | MFSD11 | chr17 | 76733119 | 76784341 |
| a0001c0001t0001g0237 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MFSD11_chr17_76733119_76784341 | MFSD11 | chr17 | 76733119 | 76784341 |
| a0001c0001t0001g0238 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MFSD11_chr17_76733119_76784341 | MFSD11 | chr17 | 76733119 | 76784341 |
| a0001c0001t0001g0239 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MFSD11_chr17_76733119_76784341 | MFSD11 | chr17 | 76733119 | 76784341 |
| a0001c0001t0001g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD11_chr17_76733119_76784341 | MFSD11 | chr17 | 76733119 | 76784341 |
| a0001c0001t0001g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD11_chr17_76733119_76784341 | MFSD11 | chr17 | 76733119 | 76784341 |
| a0001c0001t0001g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD11_chr17_76733119_76784341 | MFSD11 | chr17 | 76733119 | 76784341 |
| a0001c0001t0001g0249 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MFSD11_chr17_76733119_76784341 | MFSD11 | chr17 | 76733119 | 76784341 |
| a0001c0001t0001g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD11_chr17_76733119_76784341 | MFSD11 | chr17 | 76733119 | 76784341 |
| a0001c0001t0001g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD11_chr17_76733119_76784341 | MFSD11 | chr17 | 76733119 | 76784341 |
| a0001c0001t0001g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD11_chr17_76733119_76784341 | MFSD11 | chr17 | 76733119 | 76784341 |
| a0001c0001t0001g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD11_chr17_76733119_76784341 | MFSD11 | chr17 | 76733119 | 76784341 |
| a0001c0001t0001g0255 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MFSD11_chr17_76733119_76784341 | MFSD11 | chr17 | 76733119 | 76784341 |
| a0001c0001t0001g0256 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MFSD11_chr17_76733119_76784341 | MFSD11 | chr17 | 76733119 | 76784341 |
| a0001c0001t0001g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD11_chr17_76733119_76784341 | MFSD11 | chr17 | 76733119 | 76784341 |
| a0001c0001t0001g0258 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MFSD11_chr17_76733119_76784341 | MFSD11 | chr17 | 76733119 | 76784341 |
| a0001c0001t0001g0259 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MFSD11_chr17_76733119_76784341 | MFSD11 | chr17 | 76733119 | 76784341 |
| a0001c0001t0001g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD11_chr17_76733119_76784341 | MFSD11 | chr17 | 76733119 | 76784341 |
| a0001c0001t0001g0261 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFSD11_chr17_76733119_76784341 | MFSD11 | chr17 | 76733119 | 76784341 |
| a0001c0001t0001g0262 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MFSD11_chr17_76733119_76784341 | MFSD11 | chr17 | 76733119 | 76784341 |
| a0001c0001t0001g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD11_chr17_76733119_76784341 | MFSD11 | chr17 | 76733119 | 76784341 |
| a0001c0001t0001g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD11_chr17_76733119_76784341 | MFSD11 | chr17 | 76733119 | 76784341 |
| a0001c0001t0001g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD11_chr17_76733119_76784341 | MFSD11 | chr17 | 76733119 | 76784341 |
| a0001c0001t0001g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD11_chr17_76733119_76784341 | MFSD11 | chr17 | 76733119 | 76784341 |
| a0001c0001t0001g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD11_chr17_76733119_76784341 | MFSD11 | chr17 | 76733119 | 76784341 |
| a0001c0001t0001g0270 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MFSD11_chr17_76733119_76784341 | MFSD11 | chr17 | 76733119 | 76784341 |
| a0001c0001t0001g0272 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFSD11_chr17_76733119_76784341 | MFSD11 | chr17 | 76733119 | 76784341 |
| a0001c0001t0001g0274 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFSD11_chr17_76733119_76784341 | MFSD11 | chr17 | 76733119 | 76784341 |
| a0001c0001t0001g0275 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MFSD11_chr17_76733119_76784341 | MFSD11 | chr17 | 76733119 | 76784341 |
| a0001c0001t0001g0276 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFSD11_chr17_76733119_76784341 | MFSD11 | chr17 | 76733119 | 76784341 |
| a0001c0001t0001g0277 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFSD11_chr17_76733119_76784341 | MFSD11 | chr17 | 76733119 | 76784341 |
| a0001c0001t0001g0278 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFSD11_chr17_76733119_76784341 | MFSD11 | chr17 | 76733119 | 76784341 |
| a0001c0001t0001g0279 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFSD11_chr17_76733119_76784341 | MFSD11 | chr17 | 76733119 | 76784341 |
| a0001c0001t0001g0281 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFSD11_chr17_76733119_76784341 | MFSD11 | chr17 | 76733119 | 76784341 |
| a0001c0001t0001g0282 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFSD11_chr17_76733119_76784341 | MFSD11 | chr17 | 76733119 | 76784341 |
| a0001c0001t0001g0283 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFSD11_chr17_76733119_76784341 | MFSD11 | chr17 | 76733119 | 76784341 |
| a0001c0001t0001g0284 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFSD11_chr17_76733119_76784341 | MFSD11 | chr17 | 76733119 | 76784341 |
| a0001c0001t0001g0285 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFSD11_chr17_76733119_76784341 | MFSD11 | chr17 | 76733119 | 76784341 |
| a0001c0001t0001g0286 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MFSD11_chr17_76733119_76784341 | MFSD11 | chr17 | 76733119 | 76784341 |
| a0001c0001t0001g0287 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFSD11_chr17_76733119_76784341 | MFSD11 | chr17 | 76733119 | 76784341 |
| a0001c0001t0001g0288 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFSD11_chr17_76733119_76784341 | MFSD11 | chr17 | 76733119 | 76784341 |
| a0001c0001t0001g0290 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFSD11_chr17_76733119_76784341 | MFSD11 | chr17 | 76733119 | 76784341 |
| a0001c0001t0001g0291 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFSD11_chr17_76733119_76784341 | MFSD11 | chr17 | 76733119 | 76784341 |
| a0001c0001t0001g0292 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFSD11_chr17_76733119_76784341 | MFSD11 | chr17 | 76733119 | 76784341 |
| a0001c0001t0001g0293 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFSD11_chr17_76733119_76784341 | MFSD11 | chr17 | 76733119 | 76784341 |
| a0001c0001t0001g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD11_chr17_76733119_76784341 | MFSD11 | chr17 | 76733119 | 76784341 |
| a0001c0001t0001g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD11_chr17_76733119_76784341 | MFSD11 | chr17 | 76733119 | 76784341 |
| a0001c0001t0001g0299 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD11_chr17_76733119_76784341 | MFSD11 | chr17 | 76733119 | 76784341 |
| a0001c0001t0001g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD11_chr17_76733119_76784341 | MFSD11 | chr17 | 76733119 | 76784341 |
| a0001c0001t0001g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD11_chr17_76733119_76784341 | MFSD11 | chr17 | 76733119 | 76784341 |
| a0001c0001t0001g0302 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD11_chr17_76733119_76784341 | MFSD11 | chr17 | 76733119 | 76784341 |
| a0001c0001t0001g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD11_chr17_76733119_76784341 | MFSD11 | chr17 | 76733119 | 76784341 |
| a0001c0001t0001g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD11_chr17_76733119_76784341 | MFSD11 | chr17 | 76733119 | 76784341 |
| a0001c0001t0001g0306 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD11_chr17_76733119_76784341 | MFSD11 | chr17 | 76733119 | 76784341 |
| a0001c0001t0001g0307 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD11_chr17_76733119_76784341 | MFSD11 | chr17 | 76733119 | 76784341 |
| a0001c0001t0001g0308 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD11_chr17_76733119_76784341 | MFSD11 | chr17 | 76733119 | 76784341 |
| a0001c0001t0001g0309 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD11_chr17_76733119_76784341 | MFSD11 | chr17 | 76733119 | 76784341 |
| a0001c0001t0001g0310 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD11_chr17_76733119_76784341 | MFSD11 | chr17 | 76733119 | 76784341 |
| a0001c0001t0001g0311 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD11_chr17_76733119_76784341 | MFSD11 | chr17 | 76733119 | 76784341 |
| a0001c0001t0001g0316 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MFSD11_chr17_76733119_76784341 | MFSD11 | chr17 | 76733119 | 76784341 |
| a0001c0001t0001g0318 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MFSD11_chr17_76733119_76784341 | MFSD11 | chr17 | 76733119 | 76784341 |
| a0001c0001t0001g0320 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFSD11_chr17_76733119_76784341 | MFSD11 | chr17 | 76733119 | 76784341 |
| a0001c0001t0001g0321 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD11_chr17_76733119_76784341 | MFSD11 | chr17 | 76733119 | 76784341 |
| a0001c0001t0001g0323 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MFSD11_chr17_76733119_76784341 | MFSD11 | chr17 | 76733119 | 76784341 |
| a0001c0001t0001g0324 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFSD11_chr17_76733119_76784341 | MFSD11 | chr17 | 76733119 | 76784341 |
| a0001c0001t0001g0327 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFSD11_chr17_76733119_76784341 | MFSD11 | chr17 | 76733119 | 76784341 |
| a0001c0001t0001g0328 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFSD11_chr17_76733119_76784341 | MFSD11 | chr17 | 76733119 | 76784341 |
| a0001c0001t0001g0329 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFSD11_chr17_76733119_76784341 | MFSD11 | chr17 | 76733119 | 76784341 |
| a0001c0001t0001g0330 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD11_chr17_76733119_76784341 | MFSD11 | chr17 | 76733119 | 76784341 |
| a0001c0001t0001g0331 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MFSD11_chr17_76733119_76784341 | MFSD11 | chr17 | 76733119 | 76784341 |
| a0001c0001t0001g0332 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFSD11_chr17_76733119_76784341 | MFSD11 | chr17 | 76733119 | 76784341 |
| a0001c0001t0001g0333 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFSD11_chr17_76733119_76784341 | MFSD11 | chr17 | 76733119 | 76784341 |
| a0001c0001t0001g0334 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFSD11_chr17_76733119_76784341 | MFSD11 | chr17 | 76733119 | 76784341 |
| a0001c0001t0001g0335 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFSD11_chr17_76733119_76784341 | MFSD11 | chr17 | 76733119 | 76784341 |
| a0001c0001t0002g0001 | 0/0 | 4 | 0 | 0 | 3 | 1 | 0 | MFSD11_chr17_76733119_76784341 | MFSD11 | chr17 | 76733119 | 76784341 |
| a0001c0001t0002g0002 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | MFSD11_chr17_76733119_76784341 | MFSD11 | chr17 | 76733119 | 76784341 |
| a0001c0001t0002g0005 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MFSD11_chr17_76733119_76784341 | MFSD11 | chr17 | 76733119 | 76784341 |
| a0001c0001t0002g0006 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MFSD11_chr17_76733119_76784341 | MFSD11 | chr17 | 76733119 | 76784341 |
| a0001c0001t0002g0008 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MFSD11_chr17_76733119_76784341 | MFSD11 | chr17 | 76733119 | 76784341 |
| a0001c0001t0002g0009 | 0/0 | 2 | 0 | 0 | 1 | 1 | 0 | MFSD11_chr17_76733119_76784341 | MFSD11 | chr17 | 76733119 | 76784341 |
| a0001c0001t0002g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD11_chr17_76733119_76784341 | MFSD11 | chr17 | 76733119 | 76784341 |
| a0001c0001t0002g0059 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MFSD11_chr17_76733119_76784341 | MFSD11 | chr17 | 76733119 | 76784341 |
| a0001c0001t0002g0060 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MFSD11_chr17_76733119_76784341 | MFSD11 | chr17 | 76733119 | 76784341 |
| a0001c0001t0002g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD11_chr17_76733119_76784341 | MFSD11 | chr17 | 76733119 | 76784341 |
| a0001c0001t0002g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD11_chr17_76733119_76784341 | MFSD11 | chr17 | 76733119 | 76784341 |
| a0001c0001t0002g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD11_chr17_76733119_76784341 | MFSD11 | chr17 | 76733119 | 76784341 |
| a0001c0001t0002g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD11_chr17_76733119_76784341 | MFSD11 | chr17 | 76733119 | 76784341 |
| a0001c0001t0002g0082 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MFSD11_chr17_76733119_76784341 | MFSD11 | chr17 | 76733119 | 76784341 |
| a0001c0001t0002g0083 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MFSD11_chr17_76733119_76784341 | MFSD11 | chr17 | 76733119 | 76784341 |
| a0001c0001t0002g0084 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MFSD11_chr17_76733119_76784341 | MFSD11 | chr17 | 76733119 | 76784341 |
| a0001c0001t0002g0085 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MFSD11_chr17_76733119_76784341 | MFSD11 | chr17 | 76733119 | 76784341 |
| a0001c0001t0002g0086 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MFSD11_chr17_76733119_76784341 | MFSD11 | chr17 | 76733119 | 76784341 |
| a0001c0001t0002g0088 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MFSD11_chr17_76733119_76784341 | MFSD11 | chr17 | 76733119 | 76784341 |
| a0001c0001t0002g0089 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MFSD11_chr17_76733119_76784341 | MFSD11 | chr17 | 76733119 | 76784341 |
| a0001c0001t0002g0091 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MFSD11_chr17_76733119_76784341 | MFSD11 | chr17 | 76733119 | 76784341 |
| a0001c0001t0002g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD11_chr17_76733119_76784341 | MFSD11 | chr17 | 76733119 | 76784341 |
| a0001c0001t0002g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD11_chr17_76733119_76784341 | MFSD11 | chr17 | 76733119 | 76784341 |
| a0001c0001t0002g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD11_chr17_76733119_76784341 | MFSD11 | chr17 | 76733119 | 76784341 |
| a0001c0001t0002g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD11_chr17_76733119_76784341 | MFSD11 | chr17 | 76733119 | 76784341 |
| a0001c0001t0002g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD11_chr17_76733119_76784341 | MFSD11 | chr17 | 76733119 | 76784341 |
| a0001c0001t0002g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD11_chr17_76733119_76784341 | MFSD11 | chr17 | 76733119 | 76784341 |
| a0001c0001t0002g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD11_chr17_76733119_76784341 | MFSD11 | chr17 | 76733119 | 76784341 |
| a0001c0001t0002g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD11_chr17_76733119_76784341 | MFSD11 | chr17 | 76733119 | 76784341 |
| a0001c0001t0002g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD11_chr17_76733119_76784341 | MFSD11 | chr17 | 76733119 | 76784341 |
| a0001c0001t0002g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD11_chr17_76733119_76784341 | MFSD11 | chr17 | 76733119 | 76784341 |
| a0001c0001t0002g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD11_chr17_76733119_76784341 | MFSD11 | chr17 | 76733119 | 76784341 |
| a0001c0001t0002g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD11_chr17_76733119_76784341 | MFSD11 | chr17 | 76733119 | 76784341 |
| a0001c0001t0002g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD11_chr17_76733119_76784341 | MFSD11 | chr17 | 76733119 | 76784341 |
| a0001c0001t0002g0115 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MFSD11_chr17_76733119_76784341 | MFSD11 | chr17 | 76733119 | 76784341 |
| a0001c0001t0002g0118 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MFSD11_chr17_76733119_76784341 | MFSD11 | chr17 | 76733119 | 76784341 |
| a0001c0001t0002g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD11_chr17_76733119_76784341 | MFSD11 | chr17 | 76733119 | 76784341 |
| a0001c0001t0002g0120 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MFSD11_chr17_76733119_76784341 | MFSD11 | chr17 | 76733119 | 76784341 |
| a0001c0001t0002g0121 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MFSD11_chr17_76733119_76784341 | MFSD11 | chr17 | 76733119 | 76784341 |
| a0001c0001t0002g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD11_chr17_76733119_76784341 | MFSD11 | chr17 | 76733119 | 76784341 |
| a0001c0001t0002g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD11_chr17_76733119_76784341 | MFSD11 | chr17 | 76733119 | 76784341 |
| a0001c0001t0002g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD11_chr17_76733119_76784341 | MFSD11 | chr17 | 76733119 | 76784341 |
| a0001c0001t0002g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD11_chr17_76733119_76784341 | MFSD11 | chr17 | 76733119 | 76784341 |
| a0001c0001t0002g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD11_chr17_76733119_76784341 | MFSD11 | chr17 | 76733119 | 76784341 |
| a0001c0001t0002g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD11_chr17_76733119_76784341 | MFSD11 | chr17 | 76733119 | 76784341 |
| a0001c0001t0002g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD11_chr17_76733119_76784341 | MFSD11 | chr17 | 76733119 | 76784341 |
| a0001c0001t0002g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD11_chr17_76733119_76784341 | MFSD11 | chr17 | 76733119 | 76784341 |
| a0001c0001t0002g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD11_chr17_76733119_76784341 | MFSD11 | chr17 | 76733119 | 76784341 |
| a0001c0001t0002g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD11_chr17_76733119_76784341 | MFSD11 | chr17 | 76733119 | 76784341 |
| a0001c0001t0002g0172 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MFSD11_chr17_76733119_76784341 | MFSD11 | chr17 | 76733119 | 76784341 |
| a0001c0001t0002g0173 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MFSD11_chr17_76733119_76784341 | MFSD11 | chr17 | 76733119 | 76784341 |
| a0001c0001t0002g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD11_chr17_76733119_76784341 | MFSD11 | chr17 | 76733119 | 76784341 |
| a0001c0001t0002g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD11_chr17_76733119_76784341 | MFSD11 | chr17 | 76733119 | 76784341 |
| a0001c0001t0002g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD11_chr17_76733119_76784341 | MFSD11 | chr17 | 76733119 | 76784341 |
| a0001c0001t0002g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD11_chr17_76733119_76784341 | MFSD11 | chr17 | 76733119 | 76784341 |
| a0001c0001t0002g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD11_chr17_76733119_76784341 | MFSD11 | chr17 | 76733119 | 76784341 |
| a0001c0001t0002g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD11_chr17_76733119_76784341 | MFSD11 | chr17 | 76733119 | 76784341 |
| a0001c0001t0002g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD11_chr17_76733119_76784341 | MFSD11 | chr17 | 76733119 | 76784341 |
| a0001c0001t0002g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD11_chr17_76733119_76784341 | MFSD11 | chr17 | 76733119 | 76784341 |
| a0001c0001t0002g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD11_chr17_76733119_76784341 | MFSD11 | chr17 | 76733119 | 76784341 |
| a0001c0001t0002g0192 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MFSD11_chr17_76733119_76784341 | MFSD11 | chr17 | 76733119 | 76784341 |
| a0001c0001t0002g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD11_chr17_76733119_76784341 | MFSD11 | chr17 | 76733119 | 76784341 |
| a0001c0001t0002g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD11_chr17_76733119_76784341 | MFSD11 | chr17 | 76733119 | 76784341 |
| a0001c0001t0002g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD11_chr17_76733119_76784341 | MFSD11 | chr17 | 76733119 | 76784341 |
| a0001c0001t0002g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD11_chr17_76733119_76784341 | MFSD11 | chr17 | 76733119 | 76784341 |
| a0001c0001t0002g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD11_chr17_76733119_76784341 | MFSD11 | chr17 | 76733119 | 76784341 |
| a0001c0001t0002g0201 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MFSD11_chr17_76733119_76784341 | MFSD11 | chr17 | 76733119 | 76784341 |
| a0001c0001t0002g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD11_chr17_76733119_76784341 | MFSD11 | chr17 | 76733119 | 76784341 |
| a0001c0001t0002g0203 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MFSD11_chr17_76733119_76784341 | MFSD11 | chr17 | 76733119 | 76784341 |
| a0001c0001t0002g0204 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MFSD11_chr17_76733119_76784341 | MFSD11 | chr17 | 76733119 | 76784341 |
| a0001c0001t0002g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD11_chr17_76733119_76784341 | MFSD11 | chr17 | 76733119 | 76784341 |
| a0001c0001t0002g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD11_chr17_76733119_76784341 | MFSD11 | chr17 | 76733119 | 76784341 |
| a0001c0001t0002g0207 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MFSD11_chr17_76733119_76784341 | MFSD11 | chr17 | 76733119 | 76784341 |
| a0001c0001t0002g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD11_chr17_76733119_76784341 | MFSD11 | chr17 | 76733119 | 76784341 |
| a0001c0001t0002g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD11_chr17_76733119_76784341 | MFSD11 | chr17 | 76733119 | 76784341 |
| a0001c0001t0002g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD11_chr17_76733119_76784341 | MFSD11 | chr17 | 76733119 | 76784341 |
| a0001c0001t0002g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD11_chr17_76733119_76784341 | MFSD11 | chr17 | 76733119 | 76784341 |
| a0001c0001t0002g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD11_chr17_76733119_76784341 | MFSD11 | chr17 | 76733119 | 76784341 |
| a0001c0001t0002g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD11_chr17_76733119_76784341 | MFSD11 | chr17 | 76733119 | 76784341 |
| a0001c0001t0002g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD11_chr17_76733119_76784341 | MFSD11 | chr17 | 76733119 | 76784341 |
| a0001c0001t0002g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD11_chr17_76733119_76784341 | MFSD11 | chr17 | 76733119 | 76784341 |
| a0001c0001t0002g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD11_chr17_76733119_76784341 | MFSD11 | chr17 | 76733119 | 76784341 |
| a0001c0001t0002g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD11_chr17_76733119_76784341 | MFSD11 | chr17 | 76733119 | 76784341 |
| a0001c0001t0002g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD11_chr17_76733119_76784341 | MFSD11 | chr17 | 76733119 | 76784341 |
| a0001c0001t0002g0222 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MFSD11_chr17_76733119_76784341 | MFSD11 | chr17 | 76733119 | 76784341 |
| a0001c0001t0002g0223 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MFSD11_chr17_76733119_76784341 | MFSD11 | chr17 | 76733119 | 76784341 |
| a0001c0001t0002g0229 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MFSD11_chr17_76733119_76784341 | MFSD11 | chr17 | 76733119 | 76784341 |
| a0001c0001t0002g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD11_chr17_76733119_76784341 | MFSD11 | chr17 | 76733119 | 76784341 |
| a0001c0001t0002g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD11_chr17_76733119_76784341 | MFSD11 | chr17 | 76733119 | 76784341 |
| a0001c0001t0002g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD11_chr17_76733119_76784341 | MFSD11 | chr17 | 76733119 | 76784341 |
| a0001c0001t0002g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD11_chr17_76733119_76784341 | MFSD11 | chr17 | 76733119 | 76784341 |
| a0001c0001t0002g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD11_chr17_76733119_76784341 | MFSD11 | chr17 | 76733119 | 76784341 |
| a0001c0001t0002g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD11_chr17_76733119_76784341 | MFSD11 | chr17 | 76733119 | 76784341 |
| a0001c0001t0002g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD11_chr17_76733119_76784341 | MFSD11 | chr17 | 76733119 | 76784341 |
| a0001c0001t0002g0265 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MFSD11_chr17_76733119_76784341 | MFSD11 | chr17 | 76733119 | 76784341 |
| a0001c0001t0002g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD11_chr17_76733119_76784341 | MFSD11 | chr17 | 76733119 | 76784341 |
| a0001c0001t0002g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD11_chr17_76733119_76784341 | MFSD11 | chr17 | 76733119 | 76784341 |
| a0001c0001t0002g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD11_chr17_76733119_76784341 | MFSD11 | chr17 | 76733119 | 76784341 |
| a0001c0001t0002g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD11_chr17_76733119_76784341 | MFSD11 | chr17 | 76733119 | 76784341 |
| a0001c0001t0002g0305 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD11_chr17_76733119_76784341 | MFSD11 | chr17 | 76733119 | 76784341 |
| a0001c0001t0002g0312 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD11_chr17_76733119_76784341 | MFSD11 | chr17 | 76733119 | 76784341 |
| a0001c0001t0002g0313 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MFSD11_chr17_76733119_76784341 | MFSD11 | chr17 | 76733119 | 76784341 |
| a0001c0001t0002g0314 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MFSD11_chr17_76733119_76784341 | MFSD11 | chr17 | 76733119 | 76784341 |
| a0001c0001t0002g0315 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD11_chr17_76733119_76784341 | MFSD11 | chr17 | 76733119 | 76784341 |
| a0001c0001t0002g0317 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD11_chr17_76733119_76784341 | MFSD11 | chr17 | 76733119 | 76784341 |
| a0001c0001t0002g0319 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD11_chr17_76733119_76784341 | MFSD11 | chr17 | 76733119 | 76784341 |
| a0001c0001t0002g0322 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD11_chr17_76733119_76784341 | MFSD11 | chr17 | 76733119 | 76784341 |
| a0001c0001t0003g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFSD11_chr17_76733119_76784341 | MFSD11 | chr17 | 76733119 | 76784341 |
| a0001c0001t0003g0013 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD11_chr17_76733119_76784341 | MFSD11 | chr17 | 76733119 | 76784341 |
| a0001c0001t0003g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFSD11_chr17_76733119_76784341 | MFSD11 | chr17 | 76733119 | 76784341 |
| a0001c0001t0003g0015 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD11_chr17_76733119_76784341 | MFSD11 | chr17 | 76733119 | 76784341 |
| a0001c0001t0003g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFSD11_chr17_76733119_76784341 | MFSD11 | chr17 | 76733119 | 76784341 |
| a0001c0001t0003g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFSD11_chr17_76733119_76784341 | MFSD11 | chr17 | 76733119 | 76784341 |
| a0001c0001t0003g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFSD11_chr17_76733119_76784341 | MFSD11 | chr17 | 76733119 | 76784341 |
| a0001c0001t0003g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD11_chr17_76733119_76784341 | MFSD11 | chr17 | 76733119 | 76784341 |
| a0001c0001t0003g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFSD11_chr17_76733119_76784341 | MFSD11 | chr17 | 76733119 | 76784341 |
| a0001c0001t0003g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFSD11_chr17_76733119_76784341 | MFSD11 | chr17 | 76733119 | 76784341 |
| a0001c0001t0003g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFSD11_chr17_76733119_76784341 | MFSD11 | chr17 | 76733119 | 76784341 |
| a0001c0001t0003g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD11_chr17_76733119_76784341 | MFSD11 | chr17 | 76733119 | 76784341 |
| a0001c0001t0003g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFSD11_chr17_76733119_76784341 | MFSD11 | chr17 | 76733119 | 76784341 |
| a0001c0001t0003g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFSD11_chr17_76733119_76784341 | MFSD11 | chr17 | 76733119 | 76784341 |
| a0001c0001t0003g0026 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MFSD11_chr17_76733119_76784341 | MFSD11 | chr17 | 76733119 | 76784341 |
| a0001c0001t0003g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFSD11_chr17_76733119_76784341 | MFSD11 | chr17 | 76733119 | 76784341 |
| a0001c0001t0003g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFSD11_chr17_76733119_76784341 | MFSD11 | chr17 | 76733119 | 76784341 |
| a0001c0001t0003g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFSD11_chr17_76733119_76784341 | MFSD11 | chr17 | 76733119 | 76784341 |
| a0001c0001t0003g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFSD11_chr17_76733119_76784341 | MFSD11 | chr17 | 76733119 | 76784341 |
| a0001c0001t0004g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFSD11_chr17_76733119_76784341 | MFSD11 | chr17 | 76733119 | 76784341 |
| a0001c0001t0004g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFSD11_chr17_76733119_76784341 | MFSD11 | chr17 | 76733119 | 76784341 |
| a0001c0001t0004g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFSD11_chr17_76733119_76784341 | MFSD11 | chr17 | 76733119 | 76784341 |
| a0001c0001t0004g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFSD11_chr17_76733119_76784341 | MFSD11 | chr17 | 76733119 | 76784341 |
| a0001c0001t0004g0033 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MFSD11_chr17_76733119_76784341 | MFSD11 | chr17 | 76733119 | 76784341 |
| a0001c0001t0004g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFSD11_chr17_76733119_76784341 | MFSD11 | chr17 | 76733119 | 76784341 |
| a0001c0001t0005g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFSD11_chr17_76733119_76784341 | MFSD11 | chr17 | 76733119 | 76784341 |
| a0001c0001t0005g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFSD11_chr17_76733119_76784341 | MFSD11 | chr17 | 76733119 | 76784341 |
| a0001c0001t0005g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFSD11_chr17_76733119_76784341 | MFSD11 | chr17 | 76733119 | 76784341 |
| a0001c0001t0005g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFSD11_chr17_76733119_76784341 | MFSD11 | chr17 | 76733119 | 76784341 |
| a0001c0001t0005g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFSD11_chr17_76733119_76784341 | MFSD11 | chr17 | 76733119 | 76784341 |
| a0001c0001t0006g0325 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFSD11_chr17_76733119_76784341 | MFSD11 | chr17 | 76733119 | 76784341 |
| a0001c0001t0006g0326 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MFSD11_chr17_76733119_76784341 | MFSD11 | chr17 | 76733119 | 76784341 |
| a0001c0001t0008g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFSD11_chr17_76733119_76784341 | MFSD11 | chr17 | 76733119 | 76784341 |
| a0001c0001t0009g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MFSD11_chr17_76733119_76784341 | MFSD11 | chr17 | 76733119 | 76784341 |
| a0001c0001t0010g0090 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MFSD11_chr17_76733119_76784341 | MFSD11 | chr17 | 76733119 | 76784341 |
| a0001c0001t0011g0289 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MFSD11_chr17_76733119_76784341 | MFSD11 | chr17 | 76733119 | 76784341 |
| a0001c0001t0013g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFSD11_chr17_76733119_76784341 | MFSD11 | chr17 | 76733119 | 76784341 |
| a0001c0001t0014g0029 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | MFSD11_chr17_76733119_76784341 | MFSD11 | chr17 | 76733119 | 76784341 |
| a0001c0002t0001g0004 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MFSD11_chr17_76733119_76784341 | MFSD11 | chr17 | 76733119 | 76784341 |
| a0001c0002t0001g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFSD11_chr17_76733119_76784341 | MFSD11 | chr17 | 76733119 | 76784341 |
| a0001c0002t0001g0075 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MFSD11_chr17_76733119_76784341 | MFSD11 | chr17 | 76733119 | 76784341 |
| a0001c0002t0001g0273 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFSD11_chr17_76733119_76784341 | MFSD11 | chr17 | 76733119 | 76784341 |
| a0001c0003t0002g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFSD11_chr17_76733119_76784341 | MFSD11 | chr17 | 76733119 | 76784341 |
| a0001c0003t0002g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFSD11_chr17_76733119_76784341 | MFSD11 | chr17 | 76733119 | 76784341 |
| a0001c0003t0002g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFSD11_chr17_76733119_76784341 | MFSD11 | chr17 | 76733119 | 76784341 |
| a0001c0004t0001g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFSD11_chr17_76733119_76784341 | MFSD11 | chr17 | 76733119 | 76784341 |
| a0001c0004t0001g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFSD11_chr17_76733119_76784341 | MFSD11 | chr17 | 76733119 | 76784341 |
| a0001c0005t0001g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD11_chr17_76733119_76784341 | MFSD11 | chr17 | 76733119 | 76784341 |
| a0001c0005t0012g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD11_chr17_76733119_76784341 | MFSD11 | chr17 | 76733119 | 76784341 |
| a0001c0006t0007g0042 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MFSD11_chr17_76733119_76784341 | MFSD11 | chr17 | 76733119 | 76784341 |
| a0001c0006t0007g0043 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MFSD11_chr17_76733119_76784341 | MFSD11 | chr17 | 76733119 | 76784341 |
| a0001c0008t0001g0297 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MFSD11_chr17_76733119_76784341 | MFSD11 | chr17 | 76733119 | 76784341 |
| a0002c0007t0001g0280 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFSD11_chr17_76733119_76784341 | MFSD11 | chr17 | 76733119 | 76784341 |
| a0003c0009t0001g0166 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MFSD11_chr17_76733119_76784341 | MFSD11 | chr17 | 76733119 | 76784341 |
| a0004c0010t0001g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD11_chr17_76733119_76784341 | MFSD11 | chr17 | 76733119 | 76784341 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0001 | g0168 | EUR | GBR | MFSD11_chr17_76733119_76784341 | MFSD11 | chr17 | 76733119 | 76784341 |
| HG00099 | hp2 | a0001 | c0001 | t0001 | g0228 | EUR | GBR | MFSD11_chr17_76733119_76784341 | MFSD11 | chr17 | 76733119 | 76784341 |
| HG00140 | hp1 | a0001 | c0001 | t0001 | g0167 | EUR | GBR | MFSD11_chr17_76733119_76784341 | MFSD11 | chr17 | 76733119 | 76784341 |
| HG00140 | hp2 | a0001 | c0001 | t0002 | g0091 | EUR | GBR | MFSD11_chr17_76733119_76784341 | MFSD11 | chr17 | 76733119 | 76784341 |
| HG00280 | hp1 | a0001 | c0001 | t0001 | g0156 | EUR | FIN | MFSD11_chr17_76733119_76784341 | MFSD11 | chr17 | 76733119 | 76784341 |
| HG00280 | hp2 | a0001 | c0001 | t0002 | g0001 | EUR | FIN | MFSD11_chr17_76733119_76784341 | MFSD11 | chr17 | 76733119 | 76784341 |
| HG00323 | hp1 | a0001 | c0001 | t0002 | g0009 | EUR | FIN | MFSD11_chr17_76733119_76784341 | MFSD11 | chr17 | 76733119 | 76784341 |
| HG00323 | hp2 | a0001 | c0001 | t0001 | g0233 | EUR | FIN | MFSD11_chr17_76733119_76784341 | MFSD11 | chr17 | 76733119 | 76784341 |
| HG00423 | hp1 | a0001 | c0001 | t0002 | g0212 | EAS | CHS | MFSD11_chr17_76733119_76784341 | MFSD11 | chr17 | 76733119 | 76784341 |
| HG00423 | hp2 | a0001 | c0001 | t0001 | g0250 | EAS | CHS | MFSD11_chr17_76733119_76784341 | MFSD11 | chr17 | 76733119 | 76784341 |
| HG00544 | hp1 | a0001 | c0001 | t0001 | g0048 | EAS | CHS | MFSD11_chr17_76733119_76784341 | MFSD11 | chr17 | 76733119 | 76784341 |
| HG00544 | hp2 | a0001 | c0001 | t0001 | g0213 | EAS | CHS | MFSD11_chr17_76733119_76784341 | MFSD11 | chr17 | 76733119 | 76784341 |
| HG00558 | hp1 | a0001 | c0001 | t0002 | g0112 | EAS | CHS | MFSD11_chr17_76733119_76784341 | MFSD11 | chr17 | 76733119 | 76784341 |
| HG00558 | hp2 | a0001 | c0001 | t0002 | g0305 | EAS | CHS | MFSD11_chr17_76733119_76784341 | MFSD11 | chr17 | 76733119 | 76784341 |
| HG00597 | hp1 | a0001 | c0001 | t0001 | g0267 | EAS | CHS | MFSD11_chr17_76733119_76784341 | MFSD11 | chr17 | 76733119 | 76784341 |
| HG00597 | hp2 | a0001 | c0001 | t0002 | g0163 | EAS | CHS | MFSD11_chr17_76733119_76784341 | MFSD11 | chr17 | 76733119 | 76784341 |
| HG00609 | hp1 | a0001 | c0001 | t0002 | g0113 | EAS | CHS | MFSD11_chr17_76733119_76784341 | MFSD11 | chr17 | 76733119 | 76784341 |
| HG00609 | hp2 | a0001 | c0001 | t0002 | g0194 | EAS | CHS | MFSD11_chr17_76733119_76784341 | MFSD11 | chr17 | 76733119 | 76784341 |
| HG00621 | hp1 | a0001 | c0001 | t0002 | g0006 | EAS | CHS | MFSD11_chr17_76733119_76784341 | MFSD11 | chr17 | 76733119 | 76784341 |
| HG00621 | hp2 | a0001 | c0001 | t0001 | g0298 | EAS | CHS | MFSD11_chr17_76733119_76784341 | MFSD11 | chr17 | 76733119 | 76784341 |
| HG00639 | hp1 | a0001 | c0001 | t0001 | g0152 | AMR | PUR | MFSD11_chr17_76733119_76784341 | MFSD11 | chr17 | 76733119 | 76784341 |
| HG00639 | hp2 | a0001 | c0001 | t0001 | g0103 | AMR | PUR | MFSD11_chr17_76733119_76784341 | MFSD11 | chr17 | 76733119 | 76784341 |
| HG00642 | hp1 | a0001 | c0001 | t0001 | g0256 | AMR | PUR | MFSD11_chr17_76733119_76784341 | MFSD11 | chr17 | 76733119 | 76784341 |
| HG00642 | hp2 | a0001 | c0001 | t0001 | g0249 | AMR | PUR | MFSD11_chr17_76733119_76784341 | MFSD11 | chr17 | 76733119 | 76784341 |
| HG00673 | hp1 | a0001 | c0001 | t0001 | g0170 | EAS | CHS | MFSD11_chr17_76733119_76784341 | MFSD11 | chr17 | 76733119 | 76784341 |
| HG00673 | hp2 | a0001 | c0001 | t0002 | g0009 | EAS | CHS | MFSD11_chr17_76733119_76784341 | MFSD11 | chr17 | 76733119 | 76784341 |
| HG00733 | hp1 | a0001 | c0001 | t0001 | g0227 | AMR | PUR | MFSD11_chr17_76733119_76784341 | MFSD11 | chr17 | 76733119 | 76784341 |
| HG00733 | hp2 | a0001 | c0001 | t0001 | g0150 | AMR | PUR | MFSD11_chr17_76733119_76784341 | MFSD11 | chr17 | 76733119 | 76784341 |
| HG00735 | hp1 | a0001 | c0001 | t0001 | g0318 | AMR | PUR | MFSD11_chr17_76733119_76784341 | MFSD11 | chr17 | 76733119 | 76784341 |
| HG00735 | hp2 | a0001 | c0001 | t0001 | g0316 | AMR | PUR | MFSD11_chr17_76733119_76784341 | MFSD11 | chr17 | 76733119 | 76784341 |
| HG00741 | hp1 | a0001 | c0001 | t0001 | g0171 | AMR | PUR | MFSD11_chr17_76733119_76784341 | MFSD11 | chr17 | 76733119 | 76784341 |
| HG00741 | hp2 | a0001 | c0001 | t0001 | g0154 | AMR | PUR | MFSD11_chr17_76733119_76784341 | MFSD11 | chr17 | 76733119 | 76784341 |
| HG01069 | hp1 | a0001 | c0001 | t0004 | g0033 | AMR | PUR | MFSD11_chr17_76733119_76784341 | MFSD11 | chr17 | 76733119 | 76784341 |
| HG01069 | hp2 | a0001 | c0001 | t0001 | g0097 | AMR | PUR | MFSD11_chr17_76733119_76784341 | MFSD11 | chr17 | 76733119 | 76784341 |
| HG01070 | hp1 | a0001 | c0001 | t0001 | g0151 | AMR | PUR | MFSD11_chr17_76733119_76784341 | MFSD11 | chr17 | 76733119 | 76784341 |
| HG01070 | hp2 | a0001 | c0001 | t0002 | g0059 | AMR | PUR | MFSD11_chr17_76733119_76784341 | MFSD11 | chr17 | 76733119 | 76784341 |
| HG01071 | hp1 | a0001 | c0001 | t0002 | g0060 | AMR | PUR | MFSD11_chr17_76733119_76784341 | MFSD11 | chr17 | 76733119 | 76784341 |
| HG01071 | hp2 | a0001 | c0001 | t0001 | g0275 | AMR | PUR | MFSD11_chr17_76733119_76784341 | MFSD11 | chr17 | 76733119 | 76784341 |
| HG01074 | hp1 | a0001 | c0001 | t0001 | g0237 | AMR | PUR | MFSD11_chr17_76733119_76784341 | MFSD11 | chr17 | 76733119 | 76784341 |
| HG01074 | hp2 | a0001 | c0001 | t0001 | g0044 | AMR | PUR | MFSD11_chr17_76733119_76784341 | MFSD11 | chr17 | 76733119 | 76784341 |
| HG01081 | hp1 | a0001 | c0001 | t0002 | g0089 | AMR | PUR | MFSD11_chr17_76733119_76784341 | MFSD11 | chr17 | 76733119 | 76784341 |
| HG01081 | hp2 | a0001 | c0001 | t0009 | g0073 | AMR | PUR | MFSD11_chr17_76733119_76784341 | MFSD11 | chr17 | 76733119 | 76784341 |
| HG01099 | hp1 | a0001 | c0001 | t0006 | g0326 | AMR | PUR | MFSD11_chr17_76733119_76784341 | MFSD11 | chr17 | 76733119 | 76784341 |
| HG01099 | hp2 | a0001 | c0001 | t0001 | g0175 | AMR | PUR | MFSD11_chr17_76733119_76784341 | MFSD11 | chr17 | 76733119 | 76784341 |
| HG01106 | hp1 | a0001 | c0001 | t0001 | g0226 | AMR | PUR | MFSD11_chr17_76733119_76784341 | MFSD11 | chr17 | 76733119 | 76784341 |
| HG01106 | hp2 | a0001 | c0001 | t0003 | g0026 | AMR | PUR | MFSD11_chr17_76733119_76784341 | MFSD11 | chr17 | 76733119 | 76784341 |
| HG01109 | hp1 | a0001 | c0001 | t0002 | g0313 | AMR | PUR | MFSD11_chr17_76733119_76784341 | MFSD11 | chr17 | 76733119 | 76784341 |
| HG01109 | hp2 | a0001 | c0001 | t0001 | g0323 | AMR | PUR | MFSD11_chr17_76733119_76784341 | MFSD11 | chr17 | 76733119 | 76784341 |
| HG01168 | hp1 | a0001 | c0001 | t0002 | g0172 | AMR | PUR | MFSD11_chr17_76733119_76784341 | MFSD11 | chr17 | 76733119 | 76784341 |
| HG01168 | hp2 | a0001 | c0001 | t0001 | g0232 | AMR | PUR | MFSD11_chr17_76733119_76784341 | MFSD11 | chr17 | 76733119 | 76784341 |
| HG01169 | hp1 | a0001 | c0001 | t0002 | g0173 | AMR | PUR | MFSD11_chr17_76733119_76784341 | MFSD11 | chr17 | 76733119 | 76784341 |
| HG01169 | hp2 | a0001 | c0001 | t0001 | g0238 | AMR | PUR | MFSD11_chr17_76733119_76784341 | MFSD11 | chr17 | 76733119 | 76784341 |
| HG01192 | hp1 | a0001 | c0001 | t0001 | g0258 | AMR | PUR | MFSD11_chr17_76733119_76784341 | MFSD11 | chr17 | 76733119 | 76784341 |
| HG01192 | hp2 | a0001 | c0001 | t0001 | g0174 | AMR | PUR | MFSD11_chr17_76733119_76784341 | MFSD11 | chr17 | 76733119 | 76784341 |
| HG01243 | hp1 | a0001 | c0002 | t0001 | g0075 | AMR | PUR | MFSD11_chr17_76733119_76784341 | MFSD11 | chr17 | 76733119 | 76784341 |
| HG01243 | hp2 | a0001 | c0001 | t0001 | g0164 | AMR | PUR | MFSD11_chr17_76733119_76784341 | MFSD11 | chr17 | 76733119 | 76784341 |
| HG01258 | hp1 | a0001 | c0001 | t0001 | g0157 | AMR | CLM | MFSD11_chr17_76733119_76784341 | MFSD11 | chr17 | 76733119 | 76784341 |
| HG01258 | hp2 | a0001 | c0001 | t0001 | g0178 | AMR | CLM | MFSD11_chr17_76733119_76784341 | MFSD11 | chr17 | 76733119 | 76784341 |
| HG01361 | hp1 | a0001 | c0001 | t0001 | g0235 | AMR | CLM | MFSD11_chr17_76733119_76784341 | MFSD11 | chr17 | 76733119 | 76784341 |
| HG01361 | hp2 | a0001 | c0001 | t0002 | g0115 | AMR | CLM | MFSD11_chr17_76733119_76784341 | MFSD11 | chr17 | 76733119 | 76784341 |
| HG01496 | hp1 | a0001 | c0001 | t0001 | g0153 | AMR | CLM | MFSD11_chr17_76733119_76784341 | MFSD11 | chr17 | 76733119 | 76784341 |
| HG01496 | hp2 | a0001 | c0001 | t0001 | g0231 | AMR | CLM | MFSD11_chr17_76733119_76784341 | MFSD11 | chr17 | 76733119 | 76784341 |
| HG01517 | hp1 | a0001 | c0001 | t0001 | g0255 | EUR | IBS | MFSD11_chr17_76733119_76784341 | MFSD11 | chr17 | 76733119 | 76784341 |
| HG01517 | hp2 | a0001 | c0001 | t0001 | g0230 | EUR | IBS | MFSD11_chr17_76733119_76784341 | MFSD11 | chr17 | 76733119 | 76784341 |
| HG01884 | hp1 | a0001 | c0002 | t0001 | g0004 | AFR | ACB | MFSD11_chr17_76733119_76784341 | MFSD11 | chr17 | 76733119 | 76784341 |
| HG01884 | hp2 | a0001 | c0001 | t0006 | g0325 | AFR | ACB | MFSD11_chr17_76733119_76784341 | MFSD11 | chr17 | 76733119 | 76784341 |
| HG01891 | hp1 | a0001 | c0001 | t0003 | g0040 | AFR | ACB | MFSD11_chr17_76733119_76784341 | MFSD11 | chr17 | 76733119 | 76784341 |
| HG01891 | hp2 | a0001 | c0001 | t0001 | g0147 | AFR | ACB | MFSD11_chr17_76733119_76784341 | MFSD11 | chr17 | 76733119 | 76784341 |
| HG01928 | hp1 | a0001 | c0001 | t0002 | g0201 | AMR | PEL | MFSD11_chr17_76733119_76784341 | MFSD11 | chr17 | 76733119 | 76784341 |
| HG01928 | hp2 | a0001 | c0001 | t0002 | g0088 | AMR | PEL | MFSD11_chr17_76733119_76784341 | MFSD11 | chr17 | 76733119 | 76784341 |
| HG01975 | hp1 | a0001 | c0001 | t0010 | g0090 | AMR | PEL | MFSD11_chr17_76733119_76784341 | MFSD11 | chr17 | 76733119 | 76784341 |
| HG01975 | hp2 | a0001 | c0001 | t0001 | g0216 | AMR | PEL | MFSD11_chr17_76733119_76784341 | MFSD11 | chr17 | 76733119 | 76784341 |
| HG01978 | hp1 | a0001 | c0001 | t0001 | g0196 | AMR | PEL | MFSD11_chr17_76733119_76784341 | MFSD11 | chr17 | 76733119 | 76784341 |
| HG01978 | hp2 | a0001 | c0001 | t0002 | g0083 | AMR | PEL | MFSD11_chr17_76733119_76784341 | MFSD11 | chr17 | 76733119 | 76784341 |
| HG02004 | hp1 | a0001 | c0001 | t0002 | g0086 | AMR | PEL | MFSD11_chr17_76733119_76784341 | MFSD11 | chr17 | 76733119 | 76784341 |
| HG02004 | hp2 | a0001 | c0001 | t0001 | g0200 | AMR | PEL | MFSD11_chr17_76733119_76784341 | MFSD11 | chr17 | 76733119 | 76784341 |
| HG02015 | hp1 | a0001 | c0001 | t0002 | g0221 | EAS | KHV | MFSD11_chr17_76733119_76784341 | MFSD11 | chr17 | 76733119 | 76784341 |
| HG02015 | hp2 | a0001 | c0001 | t0002 | g0295 | EAS | KHV | MFSD11_chr17_76733119_76784341 | MFSD11 | chr17 | 76733119 | 76784341 |
| HG02027 | hp1 | a0001 | c0001 | t0002 | g0220 | EAS | KHV | MFSD11_chr17_76733119_76784341 | MFSD11 | chr17 | 76733119 | 76784341 |
| HG02027 | hp2 | a0001 | c0001 | t0001 | g0217 | EAS | KHV | MFSD11_chr17_76733119_76784341 | MFSD11 | chr17 | 76733119 | 76784341 |
| HG02040 | hp1 | a0001 | c0001 | t0001 | g0117 | EAS | KHV | MFSD11_chr17_76733119_76784341 | MFSD11 | chr17 | 76733119 | 76784341 |
| HG02040 | hp2 | a0001 | c0001 | t0002 | g0159 | EAS | KHV | MFSD11_chr17_76733119_76784341 | MFSD11 | chr17 | 76733119 | 76784341 |
| HG02055 | hp1 | a0001 | c0001 | t0001 | g0069 | AFR | ACB | MFSD11_chr17_76733119_76784341 | MFSD11 | chr17 | 76733119 | 76784341 |
| HG02055 | hp2 | a0001 | c0001 | t0001 | g0093 | AFR | ACB | MFSD11_chr17_76733119_76784341 | MFSD11 | chr17 | 76733119 | 76784341 |
| HG02056 | hp1 | a0001 | c0001 | t0001 | g0185 | EAS | KHV | MFSD11_chr17_76733119_76784341 | MFSD11 | chr17 | 76733119 | 76784341 |
| HG02056 | hp2 | a0001 | c0001 | t0002 | g0319 | EAS | KHV | MFSD11_chr17_76733119_76784341 | MFSD11 | chr17 | 76733119 | 76784341 |
| HG02071 | hp1 | a0001 | c0001 | t0002 | g0266 | EAS | KHV | MFSD11_chr17_76733119_76784341 | MFSD11 | chr17 | 76733119 | 76784341 |
| HG02071 | hp2 | a0001 | c0001 | t0002 | g0106 | EAS | KHV | MFSD11_chr17_76733119_76784341 | MFSD11 | chr17 | 76733119 | 76784341 |
| HG02074 | hp1 | a0001 | c0001 | t0001 | g0304 | EAS | KHV | MFSD11_chr17_76733119_76784341 | MFSD11 | chr17 | 76733119 | 76784341 |
| HG02074 | hp2 | a0001 | c0001 | t0002 | g0071 | EAS | KHV | MFSD11_chr17_76733119_76784341 | MFSD11 | chr17 | 76733119 | 76784341 |
| HG02080 | hp1 | a0001 | c0001 | t0002 | g0081 | EAS | KHV | MFSD11_chr17_76733119_76784341 | MFSD11 | chr17 | 76733119 | 76784341 |
| HG02080 | hp2 | a0001 | c0001 | t0001 | g0263 | EAS | KHV | MFSD11_chr17_76733119_76784341 | MFSD11 | chr17 | 76733119 | 76784341 |
| HG02083 | hp1 | a0001 | c0001 | t0002 | g0182 | EAS | KHV | MFSD11_chr17_76733119_76784341 | MFSD11 | chr17 | 76733119 | 76784341 |
| HG02083 | hp2 | a0001 | c0001 | t0001 | g0057 | EAS | KHV | MFSD11_chr17_76733119_76784341 | MFSD11 | chr17 | 76733119 | 76784341 |
| HG02132 | hp1 | a0001 | c0001 | t0002 | g0107 | EAS | KHV | MFSD11_chr17_76733119_76784341 | MFSD11 | chr17 | 76733119 | 76784341 |
| HG02132 | hp2 | a0001 | c0001 | t0002 | g0219 | EAS | KHV | MFSD11_chr17_76733119_76784341 | MFSD11 | chr17 | 76733119 | 76784341 |
| HG02135 | hp1 | a0001 | c0001 | t0002 | g0312 | EAS | KHV | MFSD11_chr17_76733119_76784341 | MFSD11 | chr17 | 76733119 | 76784341 |
| HG02135 | hp2 | a0001 | c0001 | t0001 | g0066 | EAS | KHV | MFSD11_chr17_76733119_76784341 | MFSD11 | chr17 | 76733119 | 76784341 |
| HG02145 | hp1 | a0001 | c0001 | t0001 | g0288 | AFR | ACB | MFSD11_chr17_76733119_76784341 | MFSD11 | chr17 | 76733119 | 76784341 |
| HG02145 | hp2 | a0001 | c0001 | t0001 | g0130 | AFR | ACB | MFSD11_chr17_76733119_76784341 | MFSD11 | chr17 | 76733119 | 76784341 |
| HG02148 | hp1 | a0001 | c0001 | t0001 | g0087 | AMR | PEL | MFSD11_chr17_76733119_76784341 | MFSD11 | chr17 | 76733119 | 76784341 |
| HG02148 | hp2 | a0001 | c0001 | t0001 | g0142 | AMR | PEL | MFSD11_chr17_76733119_76784341 | MFSD11 | chr17 | 76733119 | 76784341 |
| HG02155 | hp1 | a0001 | c0001 | t0001 | g0244 | EAS | CDX | MFSD11_chr17_76733119_76784341 | MFSD11 | chr17 | 76733119 | 76784341 |
| HG02155 | hp2 | a0001 | c0001 | t0001 | g0072 | EAS | CDX | MFSD11_chr17_76733119_76784341 | MFSD11 | chr17 | 76733119 | 76784341 |
| HG02165 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | CDX | MFSD11_chr17_76733119_76784341 | MFSD11 | chr17 | 76733119 | 76784341 |
| HG02165 | hp2 | a0001 | c0001 | t0001 | g0254 | EAS | CDX | MFSD11_chr17_76733119_76784341 | MFSD11 | chr17 | 76733119 | 76784341 |
| HG02257 | hp1 | a0001 | c0001 | t0001 | g0007 | AFR | ACB | MFSD11_chr17_76733119_76784341 | MFSD11 | chr17 | 76733119 | 76784341 |
| HG02257 | hp2 | a0001 | c0001 | t0001 | g0279 | AFR | ACB | MFSD11_chr17_76733119_76784341 | MFSD11 | chr17 | 76733119 | 76784341 |
| HG02258 | hp1 | a0001 | c0001 | t0003 | g0014 | AFR | ACB | MFSD11_chr17_76733119_76784341 | MFSD11 | chr17 | 76733119 | 76784341 |
| HG02258 | hp2 | a0001 | c0001 | t0004 | g0031 | AFR | ACB | MFSD11_chr17_76733119_76784341 | MFSD11 | chr17 | 76733119 | 76784341 |
| HG02273 | hp1 | a0001 | c0001 | t0002 | g0192 | AMR | PEL | MFSD11_chr17_76733119_76784341 | MFSD11 | chr17 | 76733119 | 76784341 |
| HG02273 | hp2 | a0001 | c0001 | t0001 | g0140 | AMR | PEL | MFSD11_chr17_76733119_76784341 | MFSD11 | chr17 | 76733119 | 76784341 |
| HG02293 | hp1 | a0001 | c0001 | t0001 | g0177 | AMR | PEL | MFSD11_chr17_76733119_76784341 | MFSD11 | chr17 | 76733119 | 76784341 |
| HG02293 | hp2 | a0001 | c0001 | t0002 | g0265 | AMR | PEL | MFSD11_chr17_76733119_76784341 | MFSD11 | chr17 | 76733119 | 76784341 |
| HG02300 | hp1 | a0001 | c0001 | t0001 | g0162 | AMR | PEL | MFSD11_chr17_76733119_76784341 | MFSD11 | chr17 | 76733119 | 76784341 |
| HG02300 | hp2 | a0001 | c0001 | t0001 | g0236 | AMR | PEL | MFSD11_chr17_76733119_76784341 | MFSD11 | chr17 | 76733119 | 76784341 |
| HG02572 | hp1 | a0001 | c0001 | t0003 | g0028 | AFR | GWD | MFSD11_chr17_76733119_76784341 | MFSD11 | chr17 | 76733119 | 76784341 |
| HG02572 | hp2 | a0001 | c0001 | t0001 | g0327 | AFR | GWD | MFSD11_chr17_76733119_76784341 | MFSD11 | chr17 | 76733119 | 76784341 |
| HG02602 | hp1 | a0001 | c0006 | t0007 | g0043 | SAS | PJL | MFSD11_chr17_76733119_76784341 | MFSD11 | chr17 | 76733119 | 76784341 |
| HG02602 | hp2 | a0001 | c0001 | t0001 | g0239 | SAS | PJL | MFSD11_chr17_76733119_76784341 | MFSD11 | chr17 | 76733119 | 76784341 |
| HG02615 | hp1 | a0001 | c0001 | t0003 | g0017 | AFR | GWD | MFSD11_chr17_76733119_76784341 | MFSD11 | chr17 | 76733119 | 76784341 |
| HG02615 | hp2 | a0001 | c0003 | t0002 | g0063 | AFR | GWD | MFSD11_chr17_76733119_76784341 | MFSD11 | chr17 | 76733119 | 76784341 |
| HG02622 | hp1 | a0001 | c0001 | t0001 | g0149 | AFR | GWD | MFSD11_chr17_76733119_76784341 | MFSD11 | chr17 | 76733119 | 76784341 |
| HG02622 | hp2 | a0001 | c0002 | t0001 | g0273 | AFR | GWD | MFSD11_chr17_76733119_76784341 | MFSD11 | chr17 | 76733119 | 76784341 |
| HG02630 | hp1 | a0001 | c0001 | t0005 | g0037 | AFR | GWD | MFSD11_chr17_76733119_76784341 | MFSD11 | chr17 | 76733119 | 76784341 |
| HG02630 | hp2 | a0001 | c0001 | t0004 | g0032 | AFR | GWD | MFSD11_chr17_76733119_76784341 | MFSD11 | chr17 | 76733119 | 76784341 |
| HG02647 | hp1 | a0001 | c0001 | t0001 | g0277 | AFR | GWD | MFSD11_chr17_76733119_76784341 | MFSD11 | chr17 | 76733119 | 76784341 |
| HG02647 | hp2 | a0001 | c0001 | t0003 | g0024 | AFR | GWD | MFSD11_chr17_76733119_76784341 | MFSD11 | chr17 | 76733119 | 76784341 |
| HG02683 | hp1 | a0001 | c0001 | t0001 | g0270 | SAS | PJL | MFSD11_chr17_76733119_76784341 | MFSD11 | chr17 | 76733119 | 76784341 |
| HG02683 | hp2 | a0001 | c0001 | t0002 | g0085 | SAS | PJL | MFSD11_chr17_76733119_76784341 | MFSD11 | chr17 | 76733119 | 76784341 |
| HG02698 | hp1 | a0001 | c0001 | t0001 | g0179 | SAS | PJL | MFSD11_chr17_76733119_76784341 | MFSD11 | chr17 | 76733119 | 76784341 |
| HG02698 | hp2 | a0001 | c0001 | t0001 | g0116 | SAS | PJL | MFSD11_chr17_76733119_76784341 | MFSD11 | chr17 | 76733119 | 76784341 |
| HG02717 | hp1 | a0001 | c0001 | t0003 | g0041 | AFR | GWD | MFSD11_chr17_76733119_76784341 | MFSD11 | chr17 | 76733119 | 76784341 |
| HG02717 | hp2 | a0001 | c0001 | t0001 | g0272 | AFR | GWD | MFSD11_chr17_76733119_76784341 | MFSD11 | chr17 | 76733119 | 76784341 |
| HG02723 | hp1 | a0001 | c0001 | t0004 | g0012 | AFR | GWD | MFSD11_chr17_76733119_76784341 | MFSD11 | chr17 | 76733119 | 76784341 |
| HG02723 | hp2 | a0001 | c0001 | t0001 | g0234 | AFR | GWD | MFSD11_chr17_76733119_76784341 | MFSD11 | chr17 | 76733119 | 76784341 |
| HG02735 | hp1 | a0001 | c0006 | t0007 | g0042 | SAS | PJL | MFSD11_chr17_76733119_76784341 | MFSD11 | chr17 | 76733119 | 76784341 |
| HG02735 | hp2 | a0001 | c0001 | t0001 | g0007 | SAS | PJL | MFSD11_chr17_76733119_76784341 | MFSD11 | chr17 | 76733119 | 76784341 |
| HG02738 | hp1 | a0001 | c0001 | t0001 | g0259 | SAS | PJL | MFSD11_chr17_76733119_76784341 | MFSD11 | chr17 | 76733119 | 76784341 |
| HG02738 | hp2 | a0001 | c0001 | t0011 | g0289 | SAS | PJL | MFSD11_chr17_76733119_76784341 | MFSD11 | chr17 | 76733119 | 76784341 |
| HG02809 | hp1 | a0001 | c0001 | t0001 | g0290 | AFR | GWD | MFSD11_chr17_76733119_76784341 | MFSD11 | chr17 | 76733119 | 76784341 |
| HG02809 | hp2 | a0001 | c0001 | t0001 | g0285 | AFR | GWD | MFSD11_chr17_76733119_76784341 | MFSD11 | chr17 | 76733119 | 76784341 |
| HG02818 | hp1 | a0001 | c0001 | t0003 | g0016 | AFR | GWD | MFSD11_chr17_76733119_76784341 | MFSD11 | chr17 | 76733119 | 76784341 |
| HG02818 | hp2 | a0001 | c0001 | t0001 | g0010 | AFR | GWD | MFSD11_chr17_76733119_76784341 | MFSD11 | chr17 | 76733119 | 76784341 |
| HG02886 | hp1 | a0001 | c0001 | t0004 | g0030 | AFR | GWD | MFSD11_chr17_76733119_76784341 | MFSD11 | chr17 | 76733119 | 76784341 |
| HG02886 | hp2 | a0001 | c0001 | t0005 | g0036 | AFR | GWD | MFSD11_chr17_76733119_76784341 | MFSD11 | chr17 | 76733119 | 76784341 |
| HG02895 | hp1 | a0001 | c0001 | t0001 | g0010 | AFR | GWD | MFSD11_chr17_76733119_76784341 | MFSD11 | chr17 | 76733119 | 76784341 |
| HG02895 | hp2 | a0001 | c0001 | t0013 | g0132 | AFR | GWD | MFSD11_chr17_76733119_76784341 | MFSD11 | chr17 | 76733119 | 76784341 |
| HG02896 | hp1 | a0001 | c0001 | t0001 | g0281 | AFR | GWD | MFSD11_chr17_76733119_76784341 | MFSD11 | chr17 | 76733119 | 76784341 |
| HG02896 | hp2 | a0001 | c0003 | t0002 | g0062 | AFR | GWD | MFSD11_chr17_76733119_76784341 | MFSD11 | chr17 | 76733119 | 76784341 |
| HG02897 | hp1 | a0001 | c0001 | t0001 | g0099 | AFR | GWD | MFSD11_chr17_76733119_76784341 | MFSD11 | chr17 | 76733119 | 76784341 |
| HG02897 | hp2 | a0001 | c0003 | t0002 | g0061 | AFR | GWD | MFSD11_chr17_76733119_76784341 | MFSD11 | chr17 | 76733119 | 76784341 |
| HG02922 | hp1 | a0001 | c0001 | t0003 | g0025 | AFR | ESN | MFSD11_chr17_76733119_76784341 | MFSD11 | chr17 | 76733119 | 76784341 |
| HG02922 | hp2 | a0001 | c0001 | t0008 | g0104 | AFR | ESN | MFSD11_chr17_76733119_76784341 | MFSD11 | chr17 | 76733119 | 76784341 |
| HG02965 | hp1 | a0001 | c0001 | t0001 | g0136 | AFR | ESN | MFSD11_chr17_76733119_76784341 | MFSD11 | chr17 | 76733119 | 76784341 |
| HG02965 | hp2 | a0001 | c0001 | t0001 | g0274 | AFR | ESN | MFSD11_chr17_76733119_76784341 | MFSD11 | chr17 | 76733119 | 76784341 |
| HG02970 | hp1 | a0001 | c0001 | t0001 | g0291 | AFR | ESN | MFSD11_chr17_76733119_76784341 | MFSD11 | chr17 | 76733119 | 76784341 |
| HG02970 | hp2 | a0001 | c0001 | t0001 | g0129 | AFR | ESN | MFSD11_chr17_76733119_76784341 | MFSD11 | chr17 | 76733119 | 76784341 |
| HG02976 | hp1 | a0001 | c0001 | t0003 | g0021 | AFR | ESN | MFSD11_chr17_76733119_76784341 | MFSD11 | chr17 | 76733119 | 76784341 |
| HG02976 | hp2 | a0001 | c0001 | t0001 | g0282 | AFR | ESN | MFSD11_chr17_76733119_76784341 | MFSD11 | chr17 | 76733119 | 76784341 |
| HG03017 | hp1 | a0001 | c0001 | t0002 | g0120 | SAS | PJL | MFSD11_chr17_76733119_76784341 | MFSD11 | chr17 | 76733119 | 76784341 |
| HG03017 | hp2 | a0001 | c0001 | t0002 | g0207 | SAS | PJL | MFSD11_chr17_76733119_76784341 | MFSD11 | chr17 | 76733119 | 76784341 |
| HG03041 | hp1 | a0001 | c0001 | t0001 | g0293 | AFR | GWD | MFSD11_chr17_76733119_76784341 | MFSD11 | chr17 | 76733119 | 76784341 |
| HG03041 | hp2 | a0001 | c0001 | t0001 | g0276 | AFR | GWD | MFSD11_chr17_76733119_76784341 | MFSD11 | chr17 | 76733119 | 76784341 |
| HG03098 | hp1 | a0001 | c0001 | t0001 | g0287 | AFR | MSL | MFSD11_chr17_76733119_76784341 | MFSD11 | chr17 | 76733119 | 76784341 |
| HG03098 | hp2 | a0001 | c0001 | t0001 | g0333 | AFR | MSL | MFSD11_chr17_76733119_76784341 | MFSD11 | chr17 | 76733119 | 76784341 |
| HG03130 | hp1 | a0001 | c0001 | t0001 | g0135 | AFR | ESN | MFSD11_chr17_76733119_76784341 | MFSD11 | chr17 | 76733119 | 76784341 |
| HG03130 | hp2 | a0001 | c0001 | t0003 | g0022 | AFR | ESN | MFSD11_chr17_76733119_76784341 | MFSD11 | chr17 | 76733119 | 76784341 |
| HG03139 | hp1 | a0001 | c0001 | t0001 | g0137 | AFR | ESN | MFSD11_chr17_76733119_76784341 | MFSD11 | chr17 | 76733119 | 76784341 |
| HG03139 | hp2 | a0002 | c0007 | t0001 | g0280 | AFR | ESN | MFSD11_chr17_76733119_76784341 | MFSD11 | chr17 | 76733119 | 76784341 |
| HG03195 | hp1 | a0001 | c0001 | t0001 | g0148 | AFR | ESN | MFSD11_chr17_76733119_76784341 | MFSD11 | chr17 | 76733119 | 76784341 |
| HG03195 | hp2 | a0001 | c0002 | t0001 | g0074 | AFR | ESN | MFSD11_chr17_76733119_76784341 | MFSD11 | chr17 | 76733119 | 76784341 |
| HG03209 | hp1 | a0001 | c0001 | t0005 | g0038 | AFR | MSL | MFSD11_chr17_76733119_76784341 | MFSD11 | chr17 | 76733119 | 76784341 |
| HG03209 | hp2 | a0001 | c0001 | t0001 | g0329 | AFR | MSL | MFSD11_chr17_76733119_76784341 | MFSD11 | chr17 | 76733119 | 76784341 |
| HG03225 | hp1 | a0001 | c0001 | t0001 | g0278 | AFR | MSL | MFSD11_chr17_76733119_76784341 | MFSD11 | chr17 | 76733119 | 76784341 |
| HG03225 | hp2 | a0001 | c0001 | t0001 | g0078 | AFR | MSL | MFSD11_chr17_76733119_76784341 | MFSD11 | chr17 | 76733119 | 76784341 |
| HG03453 | hp1 | a0001 | c0001 | t0001 | g0332 | AFR | MSL | MFSD11_chr17_76733119_76784341 | MFSD11 | chr17 | 76733119 | 76784341 |
| HG03453 | hp2 | a0001 | c0001 | t0001 | g0284 | AFR | MSL | MFSD11_chr17_76733119_76784341 | MFSD11 | chr17 | 76733119 | 76784341 |
| HG03490 | hp1 | a0001 | c0001 | t0001 | g0053 | SAS | PJL | MFSD11_chr17_76733119_76784341 | MFSD11 | chr17 | 76733119 | 76784341 |
| HG03490 | hp2 | a0001 | c0001 | t0002 | g0223 | SAS | PJL | MFSD11_chr17_76733119_76784341 | MFSD11 | chr17 | 76733119 | 76784341 |
| HG03492 | hp1 | a0001 | c0001 | t0002 | g0229 | SAS | PJL | MFSD11_chr17_76733119_76784341 | MFSD11 | chr17 | 76733119 | 76784341 |
| HG03492 | hp2 | a0003 | c0009 | t0001 | g0166 | SAS | PJL | MFSD11_chr17_76733119_76784341 | MFSD11 | chr17 | 76733119 | 76784341 |
| HG03516 | hp1 | a0001 | c0001 | t0001 | g0334 | AFR | ESN | MFSD11_chr17_76733119_76784341 | MFSD11 | chr17 | 76733119 | 76784341 |
| HG03516 | hp2 | a0001 | c0001 | t0001 | g0292 | AFR | ESN | MFSD11_chr17_76733119_76784341 | MFSD11 | chr17 | 76733119 | 76784341 |
| HG03540 | hp1 | a0001 | c0001 | t0001 | g0324 | AFR | GWD | MFSD11_chr17_76733119_76784341 | MFSD11 | chr17 | 76733119 | 76784341 |
| HG03540 | hp2 | a0001 | c0001 | t0004 | g0034 | AFR | GWD | MFSD11_chr17_76733119_76784341 | MFSD11 | chr17 | 76733119 | 76784341 |
| HG03579 | hp1 | a0001 | c0001 | t0001 | g0105 | AFR | MSL | MFSD11_chr17_76733119_76784341 | MFSD11 | chr17 | 76733119 | 76784341 |
| HG03579 | hp2 | a0001 | c0001 | t0005 | g0035 | AFR | MSL | MFSD11_chr17_76733119_76784341 | MFSD11 | chr17 | 76733119 | 76784341 |
| HG03688 | hp1 | a0001 | c0008 | t0001 | g0297 | SAS | STU | MFSD11_chr17_76733119_76784341 | MFSD11 | chr17 | 76733119 | 76784341 |
| HG03688 | hp2 | a0001 | c0001 | t0001 | g0055 | SAS | STU | MFSD11_chr17_76733119_76784341 | MFSD11 | chr17 | 76733119 | 76784341 |
| HG03704 | hp1 | a0001 | c0001 | t0002 | g0121 | SAS | PJL | MFSD11_chr17_76733119_76784341 | MFSD11 | chr17 | 76733119 | 76784341 |
| HG03704 | hp2 | a0001 | c0001 | t0002 | g0203 | SAS | PJL | MFSD11_chr17_76733119_76784341 | MFSD11 | chr17 | 76733119 | 76784341 |
| HG03831 | hp1 | a0001 | c0001 | t0001 | g0262 | SAS | BEB | MFSD11_chr17_76733119_76784341 | MFSD11 | chr17 | 76733119 | 76784341 |
| HG03831 | hp2 | a0001 | c0001 | t0002 | g0314 | SAS | BEB | MFSD11_chr17_76733119_76784341 | MFSD11 | chr17 | 76733119 | 76784341 |
| HG03927 | hp1 | a0001 | c0001 | t0001 | g0065 | SAS | BEB | MFSD11_chr17_76733119_76784341 | MFSD11 | chr17 | 76733119 | 76784341 |
| HG03927 | hp2 | a0001 | c0001 | t0002 | g0084 | SAS | BEB | MFSD11_chr17_76733119_76784341 | MFSD11 | chr17 | 76733119 | 76784341 |
| HG03942 | hp1 | a0001 | c0001 | t0002 | g0222 | SAS | BEB | MFSD11_chr17_76733119_76784341 | MFSD11 | chr17 | 76733119 | 76784341 |
| HG03942 | hp2 | a0001 | c0001 | t0001 | g0161 | SAS | BEB | MFSD11_chr17_76733119_76784341 | MFSD11 | chr17 | 76733119 | 76784341 |
| HG04115 | hp1 | a0001 | c0001 | t0001 | g0146 | SAS | STU | MFSD11_chr17_76733119_76784341 | MFSD11 | chr17 | 76733119 | 76784341 |
| HG04115 | hp2 | a0001 | c0001 | t0002 | g0082 | SAS | STU | MFSD11_chr17_76733119_76784341 | MFSD11 | chr17 | 76733119 | 76784341 |
| HG04184 | hp1 | a0001 | c0001 | t0002 | g0118 | SAS | BEB | MFSD11_chr17_76733119_76784341 | MFSD11 | chr17 | 76733119 | 76784341 |
| HG04184 | hp2 | a0001 | c0001 | t0001 | g0098 | SAS | BEB | MFSD11_chr17_76733119_76784341 | MFSD11 | chr17 | 76733119 | 76784341 |
| HG04228 | hp1 | a0001 | c0001 | t0001 | g0224 | SAS | STU | MFSD11_chr17_76733119_76784341 | MFSD11 | chr17 | 76733119 | 76784341 |
| HG04228 | hp2 | a0001 | c0001 | t0002 | g0204 | SAS | STU | MFSD11_chr17_76733119_76784341 | MFSD11 | chr17 | 76733119 | 76784341 |
| NA18522 | hp1 | a0001 | c0002 | t0001 | g0004 | AFR | YRI | MFSD11_chr17_76733119_76784341 | MFSD11 | chr17 | 76733119 | 76784341 |
| NA18522 | hp2 | a0001 | c0004 | t0001 | g0131 | AFR | YRI | MFSD11_chr17_76733119_76784341 | MFSD11 | chr17 | 76733119 | 76784341 |
| NA18612 | hp1 | a0001 | c0001 | t0001 | g0134 | EAS | CHB | MFSD11_chr17_76733119_76784341 | MFSD11 | chr17 | 76733119 | 76784341 |
| NA18612 | hp2 | a0001 | c0001 | t0002 | g0076 | EAS | CHB | MFSD11_chr17_76733119_76784341 | MFSD11 | chr17 | 76733119 | 76784341 |
| NA18941 | hp1 | a0001 | c0001 | t0001 | g0054 | EAS | JPT | MFSD11_chr17_76733119_76784341 | MFSD11 | chr17 | 76733119 | 76784341 |
| NA18941 | hp2 | a0001 | c0001 | t0002 | g0253 | EAS | JPT | MFSD11_chr17_76733119_76784341 | MFSD11 | chr17 | 76733119 | 76784341 |
| NA18942 | hp1 | a0001 | c0001 | t0002 | g0202 | EAS | JPT | MFSD11_chr17_76733119_76784341 | MFSD11 | chr17 | 76733119 | 76784341 |
| NA18942 | hp2 | a0001 | c0001 | t0001 | g0268 | EAS | JPT | MFSD11_chr17_76733119_76784341 | MFSD11 | chr17 | 76733119 | 76784341 |
| NA18943 | hp1 | a0004 | c0010 | t0001 | g0169 | EAS | JPT | MFSD11_chr17_76733119_76784341 | MFSD11 | chr17 | 76733119 | 76784341 |
| NA18943 | hp2 | a0001 | c0001 | t0002 | g0049 | EAS | JPT | MFSD11_chr17_76733119_76784341 | MFSD11 | chr17 | 76733119 | 76784341 |
| NA18944 | hp1 | a0001 | c0001 | t0001 | g0158 | EAS | JPT | MFSD11_chr17_76733119_76784341 | MFSD11 | chr17 | 76733119 | 76784341 |
| NA18944 | hp2 | a0001 | c0001 | t0002 | g0247 | EAS | JPT | MFSD11_chr17_76733119_76784341 | MFSD11 | chr17 | 76733119 | 76784341 |
| NA18945 | hp1 | a0001 | c0001 | t0001 | g0296 | EAS | JPT | MFSD11_chr17_76733119_76784341 | MFSD11 | chr17 | 76733119 | 76784341 |
| NA18945 | hp2 | a0001 | c0001 | t0001 | g0056 | EAS | JPT | MFSD11_chr17_76733119_76784341 | MFSD11 | chr17 | 76733119 | 76784341 |
| NA18947 | hp1 | a0001 | c0001 | t0003 | g0015 | EAS | JPT | MFSD11_chr17_76733119_76784341 | MFSD11 | chr17 | 76733119 | 76784341 |
| NA18947 | hp2 | a0001 | c0001 | t0002 | g0111 | EAS | JPT | MFSD11_chr17_76733119_76784341 | MFSD11 | chr17 | 76733119 | 76784341 |
| NA18948 | hp1 | a0001 | c0001 | t0001 | g0302 | EAS | JPT | MFSD11_chr17_76733119_76784341 | MFSD11 | chr17 | 76733119 | 76784341 |
| NA18948 | hp2 | a0001 | c0001 | t0002 | g0191 | EAS | JPT | MFSD11_chr17_76733119_76784341 | MFSD11 | chr17 | 76733119 | 76784341 |
| NA18949 | hp1 | a0001 | c0001 | t0002 | g0180 | EAS | JPT | MFSD11_chr17_76733119_76784341 | MFSD11 | chr17 | 76733119 | 76784341 |
| NA18949 | hp2 | a0001 | c0001 | t0001 | g0189 | EAS | JPT | MFSD11_chr17_76733119_76784341 | MFSD11 | chr17 | 76733119 | 76784341 |
| NA18950 | hp1 | a0001 | c0001 | t0002 | g0126 | EAS | JPT | MFSD11_chr17_76733119_76784341 | MFSD11 | chr17 | 76733119 | 76784341 |
| NA18950 | hp2 | a0001 | c0001 | t0002 | g0199 | EAS | JPT | MFSD11_chr17_76733119_76784341 | MFSD11 | chr17 | 76733119 | 76784341 |
| NA18952 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | MFSD11_chr17_76733119_76784341 | MFSD11 | chr17 | 76733119 | 76784341 |
| NA18952 | hp2 | a0001 | c0001 | t0002 | g0123 | EAS | JPT | MFSD11_chr17_76733119_76784341 | MFSD11 | chr17 | 76733119 | 76784341 |
| NA18953 | hp1 | a0001 | c0001 | t0001 | g0311 | EAS | JPT | MFSD11_chr17_76733119_76784341 | MFSD11 | chr17 | 76733119 | 76784341 |
| NA18953 | hp2 | a0001 | c0001 | t0002 | g0198 | EAS | JPT | MFSD11_chr17_76733119_76784341 | MFSD11 | chr17 | 76733119 | 76784341 |
| NA18959 | hp1 | a0001 | c0001 | t0002 | g0092 | EAS | JPT | MFSD11_chr17_76733119_76784341 | MFSD11 | chr17 | 76733119 | 76784341 |
| NA18959 | hp2 | a0001 | c0001 | t0003 | g0013 | EAS | JPT | MFSD11_chr17_76733119_76784341 | MFSD11 | chr17 | 76733119 | 76784341 |
| NA18960 | hp1 | a0001 | c0001 | t0002 | g0197 | EAS | JPT | MFSD11_chr17_76733119_76784341 | MFSD11 | chr17 | 76733119 | 76784341 |
| NA18960 | hp2 | a0001 | c0001 | t0002 | g0271 | EAS | JPT | MFSD11_chr17_76733119_76784341 | MFSD11 | chr17 | 76733119 | 76784341 |
| NA18962 | hp1 | a0001 | c0001 | t0001 | g0138 | EAS | JPT | MFSD11_chr17_76733119_76784341 | MFSD11 | chr17 | 76733119 | 76784341 |
| NA18962 | hp2 | a0001 | c0001 | t0003 | g0019 | EAS | JPT | MFSD11_chr17_76733119_76784341 | MFSD11 | chr17 | 76733119 | 76784341 |
| NA18964 | hp1 | a0001 | c0001 | t0001 | g0301 | EAS | JPT | MFSD11_chr17_76733119_76784341 | MFSD11 | chr17 | 76733119 | 76784341 |
| NA18964 | hp2 | a0001 | c0001 | t0002 | g0240 | EAS | JPT | MFSD11_chr17_76733119_76784341 | MFSD11 | chr17 | 76733119 | 76784341 |
| NA18965 | hp1 | a0001 | c0001 | t0002 | g0114 | EAS | JPT | MFSD11_chr17_76733119_76784341 | MFSD11 | chr17 | 76733119 | 76784341 |
| NA18965 | hp2 | a0001 | c0001 | t0001 | g0307 | EAS | JPT | MFSD11_chr17_76733119_76784341 | MFSD11 | chr17 | 76733119 | 76784341 |
| NA18968 | hp1 | a0001 | c0001 | t0002 | g0094 | EAS | JPT | MFSD11_chr17_76733119_76784341 | MFSD11 | chr17 | 76733119 | 76784341 |
| NA18968 | hp2 | a0001 | c0001 | t0001 | g0300 | EAS | JPT | MFSD11_chr17_76733119_76784341 | MFSD11 | chr17 | 76733119 | 76784341 |
| NA18969 | hp1 | a0001 | c0001 | t0002 | g0165 | EAS | JPT | MFSD11_chr17_76733119_76784341 | MFSD11 | chr17 | 76733119 | 76784341 |
| NA18969 | hp2 | a0001 | c0001 | t0002 | g0190 | EAS | JPT | MFSD11_chr17_76733119_76784341 | MFSD11 | chr17 | 76733119 | 76784341 |
| NA18971 | hp1 | a0001 | c0001 | t0001 | g0051 | EAS | JPT | MFSD11_chr17_76733119_76784341 | MFSD11 | chr17 | 76733119 | 76784341 |
| NA18971 | hp2 | a0001 | c0001 | t0001 | g0306 | EAS | JPT | MFSD11_chr17_76733119_76784341 | MFSD11 | chr17 | 76733119 | 76784341 |
| NA18972 | hp1 | a0001 | c0001 | t0002 | g0246 | EAS | JPT | MFSD11_chr17_76733119_76784341 | MFSD11 | chr17 | 76733119 | 76784341 |
| NA18972 | hp2 | a0001 | c0001 | t0002 | g0315 | EAS | JPT | MFSD11_chr17_76733119_76784341 | MFSD11 | chr17 | 76733119 | 76784341 |
| NA18974 | hp1 | a0001 | c0001 | t0002 | g0006 | EAS | JPT | MFSD11_chr17_76733119_76784341 | MFSD11 | chr17 | 76733119 | 76784341 |
| NA18974 | hp2 | a0001 | c0001 | t0001 | g0046 | EAS | JPT | MFSD11_chr17_76733119_76784341 | MFSD11 | chr17 | 76733119 | 76784341 |
| NA18977 | hp1 | a0001 | c0001 | t0002 | g0294 | EAS | JPT | MFSD11_chr17_76733119_76784341 | MFSD11 | chr17 | 76733119 | 76784341 |
| NA18977 | hp2 | a0001 | c0001 | t0001 | g0330 | EAS | JPT | MFSD11_chr17_76733119_76784341 | MFSD11 | chr17 | 76733119 | 76784341 |
| NA18979 | hp1 | a0001 | c0001 | t0002 | g0008 | EAS | JPT | MFSD11_chr17_76733119_76784341 | MFSD11 | chr17 | 76733119 | 76784341 |
| NA18979 | hp2 | a0001 | c0001 | t0001 | g0067 | EAS | JPT | MFSD11_chr17_76733119_76784341 | MFSD11 | chr17 | 76733119 | 76784341 |
| NA18980 | hp1 | a0001 | c0001 | t0001 | g0264 | EAS | JPT | MFSD11_chr17_76733119_76784341 | MFSD11 | chr17 | 76733119 | 76784341 |
| NA18980 | hp2 | a0001 | c0001 | t0002 | g0109 | EAS | JPT | MFSD11_chr17_76733119_76784341 | MFSD11 | chr17 | 76733119 | 76784341 |
| NA18981 | hp1 | a0001 | c0001 | t0001 | g0155 | EAS | JPT | MFSD11_chr17_76733119_76784341 | MFSD11 | chr17 | 76733119 | 76784341 |
| NA18981 | hp2 | a0001 | c0001 | t0002 | g0245 | EAS | JPT | MFSD11_chr17_76733119_76784341 | MFSD11 | chr17 | 76733119 | 76784341 |
| NA18983 | hp1 | a0001 | c0001 | t0002 | g0208 | EAS | JPT | MFSD11_chr17_76733119_76784341 | MFSD11 | chr17 | 76733119 | 76784341 |
| NA18983 | hp2 | a0001 | c0001 | t0002 | g0211 | EAS | JPT | MFSD11_chr17_76733119_76784341 | MFSD11 | chr17 | 76733119 | 76784341 |
| NA18984 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | MFSD11_chr17_76733119_76784341 | MFSD11 | chr17 | 76733119 | 76784341 |
| NA18984 | hp2 | a0001 | c0001 | t0001 | g0050 | EAS | JPT | MFSD11_chr17_76733119_76784341 | MFSD11 | chr17 | 76733119 | 76784341 |
| NA18990 | hp1 | a0001 | c0001 | t0001 | g0188 | EAS | JPT | MFSD11_chr17_76733119_76784341 | MFSD11 | chr17 | 76733119 | 76784341 |
| NA18990 | hp2 | a0001 | c0001 | t0001 | g0242 | EAS | JPT | MFSD11_chr17_76733119_76784341 | MFSD11 | chr17 | 76733119 | 76784341 |
| NA18991 | hp1 | a0001 | c0001 | t0001 | g0133 | EAS | JPT | MFSD11_chr17_76733119_76784341 | MFSD11 | chr17 | 76733119 | 76784341 |
| NA18991 | hp2 | a0001 | c0001 | t0001 | g0070 | EAS | JPT | MFSD11_chr17_76733119_76784341 | MFSD11 | chr17 | 76733119 | 76784341 |
| NA18993 | hp1 | a0001 | c0001 | t0001 | g0251 | EAS | JPT | MFSD11_chr17_76733119_76784341 | MFSD11 | chr17 | 76733119 | 76784341 |
| NA18993 | hp2 | a0001 | c0001 | t0001 | g0252 | EAS | JPT | MFSD11_chr17_76733119_76784341 | MFSD11 | chr17 | 76733119 | 76784341 |
| NA18994 | hp1 | a0001 | c0001 | t0001 | g0101 | EAS | JPT | MFSD11_chr17_76733119_76784341 | MFSD11 | chr17 | 76733119 | 76784341 |
| NA18994 | hp2 | a0001 | c0001 | t0002 | g0096 | EAS | JPT | MFSD11_chr17_76733119_76784341 | MFSD11 | chr17 | 76733119 | 76784341 |
| NA18998 | hp1 | a0001 | c0001 | t0002 | g0119 | EAS | JPT | MFSD11_chr17_76733119_76784341 | MFSD11 | chr17 | 76733119 | 76784341 |
| NA18998 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | MFSD11_chr17_76733119_76784341 | MFSD11 | chr17 | 76733119 | 76784341 |
| NA18999 | hp1 | a0001 | c0001 | t0002 | g0005 | EAS | JPT | MFSD11_chr17_76733119_76784341 | MFSD11 | chr17 | 76733119 | 76784341 |
| NA18999 | hp2 | a0001 | c0001 | t0002 | g0008 | EAS | JPT | MFSD11_chr17_76733119_76784341 | MFSD11 | chr17 | 76733119 | 76784341 |
| NA19000 | hp1 | a0001 | c0001 | t0001 | g0260 | EAS | JPT | MFSD11_chr17_76733119_76784341 | MFSD11 | chr17 | 76733119 | 76784341 |
| NA19000 | hp2 | a0001 | c0001 | t0002 | g0184 | EAS | JPT | MFSD11_chr17_76733119_76784341 | MFSD11 | chr17 | 76733119 | 76784341 |
| NA19001 | hp1 | a0001 | c0001 | t0002 | g0317 | EAS | JPT | MFSD11_chr17_76733119_76784341 | MFSD11 | chr17 | 76733119 | 76784341 |
| NA19001 | hp2 | a0001 | c0001 | t0001 | g0257 | EAS | JPT | MFSD11_chr17_76733119_76784341 | MFSD11 | chr17 | 76733119 | 76784341 |
| NA19002 | hp1 | a0001 | c0001 | t0001 | g0269 | EAS | JPT | MFSD11_chr17_76733119_76784341 | MFSD11 | chr17 | 76733119 | 76784341 |
| NA19002 | hp2 | a0001 | c0001 | t0001 | g0243 | EAS | JPT | MFSD11_chr17_76733119_76784341 | MFSD11 | chr17 | 76733119 | 76784341 |
| NA19003 | hp1 | a0001 | c0001 | t0001 | g0141 | EAS | JPT | MFSD11_chr17_76733119_76784341 | MFSD11 | chr17 | 76733119 | 76784341 |
| NA19003 | hp2 | a0001 | c0001 | t0002 | g0210 | EAS | JPT | MFSD11_chr17_76733119_76784341 | MFSD11 | chr17 | 76733119 | 76784341 |
| NA19007 | hp1 | a0001 | c0001 | t0002 | g0110 | EAS | JPT | MFSD11_chr17_76733119_76784341 | MFSD11 | chr17 | 76733119 | 76784341 |
| NA19007 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | MFSD11_chr17_76733119_76784341 | MFSD11 | chr17 | 76733119 | 76784341 |
| NA19009 | hp1 | a0001 | c0001 | t0002 | g0248 | EAS | JPT | MFSD11_chr17_76733119_76784341 | MFSD11 | chr17 | 76733119 | 76784341 |
| NA19009 | hp2 | a0001 | c0001 | t0001 | g0128 | EAS | JPT | MFSD11_chr17_76733119_76784341 | MFSD11 | chr17 | 76733119 | 76784341 |
| NA19010 | hp1 | a0001 | c0001 | t0002 | g0144 | EAS | JPT | MFSD11_chr17_76733119_76784341 | MFSD11 | chr17 | 76733119 | 76784341 |
| NA19010 | hp2 | a0001 | c0001 | t0002 | g0186 | EAS | JPT | MFSD11_chr17_76733119_76784341 | MFSD11 | chr17 | 76733119 | 76784341 |
| NA19011 | hp1 | a0001 | c0001 | t0002 | g0183 | EAS | JPT | MFSD11_chr17_76733119_76784341 | MFSD11 | chr17 | 76733119 | 76784341 |
| NA19011 | hp2 | a0001 | c0001 | t0001 | g0068 | EAS | JPT | MFSD11_chr17_76733119_76784341 | MFSD11 | chr17 | 76733119 | 76784341 |
| NA19030 | hp1 | a0001 | c0004 | t0001 | g0100 | AFR | LWK | MFSD11_chr17_76733119_76784341 | MFSD11 | chr17 | 76733119 | 76784341 |
| NA19030 | hp2 | a0001 | c0001 | t0001 | g0320 | AFR | LWK | MFSD11_chr17_76733119_76784341 | MFSD11 | chr17 | 76733119 | 76784341 |
| NA19043 | hp1 | a0001 | c0001 | t0001 | g0283 | AFR | LWK | MFSD11_chr17_76733119_76784341 | MFSD11 | chr17 | 76733119 | 76784341 |
| NA19043 | hp2 | a0001 | c0001 | t0001 | g0335 | AFR | LWK | MFSD11_chr17_76733119_76784341 | MFSD11 | chr17 | 76733119 | 76784341 |
| NA19055 | hp1 | a0001 | c0001 | t0002 | g0206 | EAS | JPT | MFSD11_chr17_76733119_76784341 | MFSD11 | chr17 | 76733119 | 76784341 |
| NA19055 | hp2 | a0001 | c0001 | t0002 | g0005 | EAS | JPT | MFSD11_chr17_76733119_76784341 | MFSD11 | chr17 | 76733119 | 76784341 |
| NA19056 | hp1 | a0001 | c0001 | t0001 | g0310 | EAS | JPT | MFSD11_chr17_76733119_76784341 | MFSD11 | chr17 | 76733119 | 76784341 |
| NA19056 | hp2 | a0001 | c0001 | t0002 | g0209 | EAS | JPT | MFSD11_chr17_76733119_76784341 | MFSD11 | chr17 | 76733119 | 76784341 |
| NA19060 | hp1 | a0001 | c0005 | t0012 | g0195 | EAS | JPT | MFSD11_chr17_76733119_76784341 | MFSD11 | chr17 | 76733119 | 76784341 |
| NA19060 | hp2 | a0001 | c0001 | t0002 | g0241 | EAS | JPT | MFSD11_chr17_76733119_76784341 | MFSD11 | chr17 | 76733119 | 76784341 |
| NA19062 | hp1 | a0001 | c0001 | t0002 | g0187 | EAS | JPT | MFSD11_chr17_76733119_76784341 | MFSD11 | chr17 | 76733119 | 76784341 |
| NA19062 | hp2 | a0001 | c0001 | t0001 | g0047 | EAS | JPT | MFSD11_chr17_76733119_76784341 | MFSD11 | chr17 | 76733119 | 76784341 |
| NA19064 | hp1 | a0001 | c0001 | t0002 | g0322 | EAS | JPT | MFSD11_chr17_76733119_76784341 | MFSD11 | chr17 | 76733119 | 76784341 |
| NA19064 | hp2 | a0001 | c0001 | t0001 | g0303 | EAS | JPT | MFSD11_chr17_76733119_76784341 | MFSD11 | chr17 | 76733119 | 76784341 |
| NA19065 | hp1 | a0001 | c0001 | t0002 | g0077 | EAS | JPT | MFSD11_chr17_76733119_76784341 | MFSD11 | chr17 | 76733119 | 76784341 |
| NA19065 | hp2 | a0001 | c0001 | t0002 | g0125 | EAS | JPT | MFSD11_chr17_76733119_76784341 | MFSD11 | chr17 | 76733119 | 76784341 |
| NA19066 | hp1 | a0001 | c0001 | t0002 | g0108 | EAS | JPT | MFSD11_chr17_76733119_76784341 | MFSD11 | chr17 | 76733119 | 76784341 |
| NA19066 | hp2 | a0001 | c0001 | t0001 | g0139 | EAS | JPT | MFSD11_chr17_76733119_76784341 | MFSD11 | chr17 | 76733119 | 76784341 |
| NA19070 | hp1 | a0001 | c0001 | t0001 | g0308 | EAS | JPT | MFSD11_chr17_76733119_76784341 | MFSD11 | chr17 | 76733119 | 76784341 |
| NA19070 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | MFSD11_chr17_76733119_76784341 | MFSD11 | chr17 | 76733119 | 76784341 |
| NA19074 | hp1 | a0001 | c0001 | t0002 | g0215 | EAS | JPT | MFSD11_chr17_76733119_76784341 | MFSD11 | chr17 | 76733119 | 76784341 |
| NA19074 | hp2 | a0001 | c0001 | t0002 | g0122 | EAS | JPT | MFSD11_chr17_76733119_76784341 | MFSD11 | chr17 | 76733119 | 76784341 |
| NA19075 | hp1 | a0001 | c0005 | t0001 | g0102 | EAS | JPT | MFSD11_chr17_76733119_76784341 | MFSD11 | chr17 | 76733119 | 76784341 |
| NA19075 | hp2 | a0001 | c0001 | t0003 | g0023 | EAS | JPT | MFSD11_chr17_76733119_76784341 | MFSD11 | chr17 | 76733119 | 76784341 |
| NA19077 | hp1 | a0001 | c0001 | t0001 | g0321 | EAS | JPT | MFSD11_chr17_76733119_76784341 | MFSD11 | chr17 | 76733119 | 76784341 |
| NA19077 | hp2 | a0001 | c0001 | t0002 | g0218 | EAS | JPT | MFSD11_chr17_76733119_76784341 | MFSD11 | chr17 | 76733119 | 76784341 |
| NA19079 | hp1 | a0001 | c0001 | t0002 | g0214 | EAS | JPT | MFSD11_chr17_76733119_76784341 | MFSD11 | chr17 | 76733119 | 76784341 |
| NA19079 | hp2 | a0001 | c0001 | t0001 | g0058 | EAS | JPT | MFSD11_chr17_76733119_76784341 | MFSD11 | chr17 | 76733119 | 76784341 |
| NA19080 | hp1 | a0001 | c0001 | t0002 | g0193 | EAS | JPT | MFSD11_chr17_76733119_76784341 | MFSD11 | chr17 | 76733119 | 76784341 |
| NA19080 | hp2 | a0001 | c0001 | t0002 | g0127 | EAS | JPT | MFSD11_chr17_76733119_76784341 | MFSD11 | chr17 | 76733119 | 76784341 |
| NA19081 | hp1 | a0001 | c0001 | t0001 | g0299 | EAS | JPT | MFSD11_chr17_76733119_76784341 | MFSD11 | chr17 | 76733119 | 76784341 |
| NA19081 | hp2 | a0001 | c0001 | t0002 | g0181 | EAS | JPT | MFSD11_chr17_76733119_76784341 | MFSD11 | chr17 | 76733119 | 76784341 |
| NA19088 | hp1 | a0001 | c0001 | t0001 | g0143 | EAS | JPT | MFSD11_chr17_76733119_76784341 | MFSD11 | chr17 | 76733119 | 76784341 |
| NA19088 | hp2 | a0001 | c0001 | t0002 | g0124 | EAS | JPT | MFSD11_chr17_76733119_76784341 | MFSD11 | chr17 | 76733119 | 76784341 |
| NA19090 | hp1 | a0001 | c0001 | t0002 | g0205 | EAS | JPT | MFSD11_chr17_76733119_76784341 | MFSD11 | chr17 | 76733119 | 76784341 |
| NA19090 | hp2 | a0001 | c0001 | t0001 | g0064 | EAS | JPT | MFSD11_chr17_76733119_76784341 | MFSD11 | chr17 | 76733119 | 76784341 |
| NA20752 | hp1 | a0001 | c0001 | t0001 | g0003 | EUR | TSI | MFSD11_chr17_76733119_76784341 | MFSD11 | chr17 | 76733119 | 76784341 |
| NA20752 | hp2 | a0001 | c0001 | t0001 | g0331 | EUR | TSI | MFSD11_chr17_76733119_76784341 | MFSD11 | chr17 | 76733119 | 76784341 |
| NA20805 | hp1 | a0001 | c0001 | t0001 | g0160 | EUR | TSI | MFSD11_chr17_76733119_76784341 | MFSD11 | chr17 | 76733119 | 76784341 |
| NA20805 | hp2 | a0001 | c0001 | t0001 | g0003 | EUR | TSI | MFSD11_chr17_76733119_76784341 | MFSD11 | chr17 | 76733119 | 76784341 |
| HG01123 | hp1 | a0001 | c0001 | t0001 | g0052 | AMR | CLM | MFSD11_chr17_76733119_76784341 | MFSD11 | chr17 | 76733119 | 76784341 |
| HG01123 | hp2 | a0001 | c0001 | t0001 | g0286 | AMR | CLM | MFSD11_chr17_76733119_76784341 | MFSD11 | chr17 | 76733119 | 76784341 |
| HG02109 | hp1 | a0001 | c0001 | t0001 | g0080 | AFR | ACB | MFSD11_chr17_76733119_76784341 | MFSD11 | chr17 | 76733119 | 76784341 |
| HG02109 | hp2 | a0001 | c0001 | t0003 | g0027 | AFR | ACB | MFSD11_chr17_76733119_76784341 | MFSD11 | chr17 | 76733119 | 76784341 |
| HG02486 | hp1 | a0001 | c0001 | t0001 | g0225 | AFR | ACB | MFSD11_chr17_76733119_76784341 | MFSD11 | chr17 | 76733119 | 76784341 |
| HG02486 | hp2 | a0001 | c0001 | t0003 | g0011 | AFR | ACB | MFSD11_chr17_76733119_76784341 | MFSD11 | chr17 | 76733119 | 76784341 |
| HG02559 | hp1 | a0001 | c0001 | t0003 | g0020 | AFR | ACB | MFSD11_chr17_76733119_76784341 | MFSD11 | chr17 | 76733119 | 76784341 |
| HG02559 | hp2 | a0001 | c0001 | t0003 | g0018 | AFR | ACB | MFSD11_chr17_76733119_76784341 | MFSD11 | chr17 | 76733119 | 76784341 |
| HG03471 | hp1 | a0001 | c0001 | t0005 | g0039 | AFR | MSL | MFSD11_chr17_76733119_76784341 | MFSD11 | chr17 | 76733119 | 76784341 |
| HG03471 | hp2 | a0001 | c0001 | t0001 | g0079 | AFR | MSL | MFSD11_chr17_76733119_76784341 | MFSD11 | chr17 | 76733119 | 76784341 |
| HG06807 | hp1 | a0001 | c0001 | t0001 | g0176 | AFR | USA | MFSD11_chr17_76733119_76784341 | MFSD11 | chr17 | 76733119 | 76784341 |
| HG06807 | hp2 | a0001 | c0001 | t0001 | g0328 | AFR | USA | MFSD11_chr17_76733119_76784341 | MFSD11 | chr17 | 76733119 | 76784341 |
| NA18955 | hp1 | a0001 | c0001 | t0002 | g0095 | EAS | JPT | MFSD11_chr17_76733119_76784341 | MFSD11 | chr17 | 76733119 | 76784341 |
| NA18955 | hp2 | a0001 | c0001 | t0001 | g0309 | EAS | JPT | MFSD11_chr17_76733119_76784341 | MFSD11 | chr17 | 76733119 | 76784341 |
| NA20300 | hp1 | a0001 | c0001 | t0001 | g0261 | AFR | USA | MFSD11_chr17_76733119_76784341 | MFSD11 | chr17 | 76733119 | 76784341 |
| NA20300 | hp2 | a0001 | c0001 | t0001 | g0145 | AFR | USA | MFSD11_chr17_76733119_76784341 | MFSD11 | chr17 | 76733119 | 76784341 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0001 | g0045 | REF | REF | MFSD11_chr17_76733119_76784341 | MFSD11 | chr17 | 76733119 | 76784341 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0014 | g0029 | REF | REF | MFSD11_chr17_76733119_76784341 | MFSD11 | chr17 | 76733119 | 76784341 |
| view | chr:pos | ref | alt | # # of ahapid:amino-acid(protein) level |
ahapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr17:76744355 | C | T | 1 | a0004 | 1 | NA18943.hp1 | missense_variant | MODERATE | c.530C>T | p.Thr177Met | MFSD11 | ENSG00000092931.12 | transcript | ENST00000685175.1 | protein_coding | 7/13 | 764/2573 | 530/1350 | 177/449 | chr17 | 76744355 | |||
| chr17:76744414 | A | G | 1 | a0003 | 1 | HG03492.hp2 | missense_variant | MODERATE | c.589A>G | p.Asn197Asp | MFSD11 | ENSG00000092931.12 | transcript | ENST00000685175.1 | protein_coding | 7/13 | 823/2573 | 589/1350 | 197/449 | chr17 | 76744414 | |||
| chr17:76775024 | A | T | 1 | a0002 | 1 | HG03139.hp2 | missense_variant | MODERATE | c.902A>T | p.Lys301Met | MFSD11 | ENSG00000092931.12 | transcript | ENST00000685175.1 | protein_coding | 11/13 | 1136/2573 | 902/1350 | 301/449 | chr17 | 76775024 |
| view | chr:pos | ref | alt | # # of chapid |
chapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr17:76742217 | G | A | 1 | a0001c0003 | 3 | HG02615.hp2 HG02896.hp2 HG02897.hp2 |
synonymous_variant | LOW | c.381G>A | p.Ser127Ser | MFSD11 | ENSG00000092931.12 | transcript | ENST00000685175.1 | protein_coding | 5/13 | 615/2573 | 381/1350 | 127/449 | chr17 | 76742217 | |||
| chr17:76744383 | A | G | 1 | a0001c0006 | 2 | HG02602.hp1 HG02735.hp1 |
synonymous_variant | LOW | c.558A>G | p.Leu186Leu | MFSD11 | ENSG00000092931.12 | transcript | ENST00000685175.1 | protein_coding | 7/13 | 792/2573 | 558/1350 | 186/449 | chr17 | 76744383 | |||
| chr17:76769774 | A | C | 1 | a0001c0008 | 1 | HG03688.hp1 | synonymous_variant | LOW | c.777A>C | p.Val259Val | MFSD11 | ENSG00000092931.12 | transcript | ENST00000685175.1 | protein_coding | 10/13 | 1011/2573 | 777/1350 | 259/449 | chr17 | 76769774 | |||
| chr17:76776466 | C | T | 1 | a0001c0002 | 5 | HG01243.hp1 HG01884.hp1 HG02622.hp2 others(2): Show |
synonymous_variant | LOW | c.1110C>T | p.Thr370Thr | MFSD11 | ENSG00000092931.12 | transcript | ENST00000685175.1 | protein_coding | 12/13 | 1344/2573 | 1110/1350 | 370/449 | chr17 | 76776466 | |||
| chr17:76776491 | C | T | 1 | a0001c0005 | 2 | NA19060.hp1 NA19075.hp1 |
synonymous_variant | LOW | c.1135C>T | p.Leu379Leu | MFSD11 | ENSG00000092931.12 | transcript | ENST00000685175.1 | protein_coding | 12/13 | 1369/2573 | 1135/1350 | 379/449 | chr17 | 76776491 | |||
| chr17:76778328 | C | T | 1 | a0001c0004 | 2 | NA18522.hp2 NA19030.hp1 |
synonymous_variant | LOW | c.1326C>T | p.Arg442Arg | MFSD11 | ENSG00000092931.12 | transcript | ENST00000685175.1 | protein_coding | 13/13 | 1560/2573 | 1326/1350 | 442/449 | chr17 | 76778328 |
| view | chr:pos | ref | alt | # # of thapid:transcript level |
thapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr17:76738241 | G | A | 17 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0006 others(14): Show |
314 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(311): Show |
5_prime_UTR_variant | MODIFIER | c.-112G>A | MFSD11 | ENSG00000092931.12 | transcript | ENST00000685175.1 | protein_coding | 1/13 | 112 | chr17 | 76738241 | ||||||
| chr17:76738303 | G | A | 1 | a0001c0001t0008 | 1 | HG02922.hp2 | 5_prime_UTR_variant | MODIFIER | c.-50G>A | MFSD11 | ENSG00000092931.12 | transcript | ENST00000685175.1 | protein_coding | 1/13 | 50 | chr17 | 76738303 | ||||||
| chr17:76778482 | C | G | 1 | a0001c0001t0004 | 6 | HG01069.hp1 HG02258.hp2 HG02630.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*130C>G | MFSD11 | ENSG00000092931.12 | transcript | ENST00000685175.1 | protein_coding | 13/13 | 130 | chr17 | 76778482 | ||||||
| chr17:76778511 | G | A | 1 | a0001c0001t0009 | 1 | HG01081.hp2 | 3_prime_UTR_variant | MODIFIER | c.*159G>A | MFSD11 | ENSG00000092931.12 | transcript | ENST00000685175.1 | protein_coding | 13/13 | 159 | chr17 | 76778511 | ||||||
| chr17:76778743 | C | T | 17 | a0001c0001t0001 a0001c0001t0003 a0001c0001t0004 others(14): Show |
225 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(222): Show |
3_prime_UTR_variant | MODIFIER | c.*391C>T | MFSD11 | ENSG00000092931.12 | transcript | ENST00000685175.1 | protein_coding | 13/13 | 391 | chr17 | 76778743 | ||||||
| chr17:76778824 | G | T | 1 | a0001c0001t0005 | 5 | HG02630.hp1 HG02886.hp2 HG03209.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*472G>T | MFSD11 | ENSG00000092931.12 | transcript | ENST00000685175.1 | protein_coding | 13/13 | 472 | chr17 | 76778824 | ||||||
| chr17:76778899 | G | T | 1 | a0001c0001t0013 | 1 | HG02895.hp2 | 3_prime_UTR_variant | MODIFIER | c.*547G>T | MFSD11 | ENSG00000092931.12 | transcript | ENST00000685175.1 | protein_coding | 13/13 | 547 | chr17 | 76778899 | ||||||
| chr17:76779004 | A | G | 1 | a0001c0001t0006 | 2 | HG01099.hp1 HG01884.hp2 |
3_prime_UTR_variant | MODIFIER | c.*652A>G | MFSD11 | ENSG00000092931.12 | transcript | ENST00000685175.1 | protein_coding | 13/13 | 652 | chr17 | 76779004 | ||||||
| chr17:76779138 | A | G | 1 | a0001c0006t0007 | 2 | HG02602.hp1 HG02735.hp1 |
3_prime_UTR_variant | MODIFIER | c.*786A>G | MFSD11 | ENSG00000092931.12 | transcript | ENST00000685175.1 | protein_coding | 13/13 | 786 | chr17 | 76779138 | ||||||
| chr17:76779156 | G | A | 1 | a0001c0001t0011 | 1 | HG02738.hp2 | 3_prime_UTR_variant | MODIFIER | c.*804G>A | MFSD11 | ENSG00000092931.12 | transcript | ENST00000685175.1 | protein_coding | 13/13 | 804 | chr17 | 76779156 | ||||||
| chr17:76779222 | C | G | 1 | a0001c0001t0013 | 1 | HG02895.hp2 | 3_prime_UTR_variant | MODIFIER | c.*870C>G | MFSD11 | ENSG00000092931.12 | transcript | ENST00000685175.1 | protein_coding | 13/13 | 870 | chr17 | 76779222 | ||||||
| chr17:76779254 | C | CA | 7 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0004 others(4): Show |
24 | HG00423.hp1 HG01069.hp1 HG01099.hp1 others(21): Show |
3_prime_UTR_variant | MODIFIER | c.*922dupA | MFSD11 | ENSG00000092931.12 | transcript | ENST00000685175.1 | protein_coding | 13/13 | 923 | INFO_REALIGN_3_PRIME | chr17 | 76779254 | |||||
| chr17:76779254 | CA | C | 2 | a0001c0001t0001 a0001c0001t0002 |
7 | HG00558.hp1 HG01168.hp1 HG02165.hp1 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*922delA | MFSD11 | ENSG00000092931.12 | transcript | ENST00000685175.1 | protein_coding | 13/13 | 922 | INFO_REALIGN_3_PRIME | chr17 | 76779254 | |||||
| chr17:76779269 | A | G | 1 | a0001c0001t0010 | 1 | HG01975.hp1 | 3_prime_UTR_variant | MODIFIER | c.*917A>G | MFSD11 | ENSG00000092931.12 | transcript | ENST00000685175.1 | protein_coding | 13/13 | 917 | chr17 | 76779269 | ||||||
| chr17:76779274 | A | G | 1 | a0001c0005t0012 | 1 | NA19060.hp1 | 3_prime_UTR_variant | MODIFIER | c.*922A>G | MFSD11 | ENSG00000092931.12 | transcript | ENST00000685175.1 | protein_coding | 13/13 | 922 | chr17 | 76779274 | ||||||
| chr17:76779275 | G | A | 1 | a0001c0005t0012 | 1 | NA19060.hp1 | 3_prime_UTR_variant | MODIFIER | c.*923G>A | MFSD11 | ENSG00000092931.12 | transcript | ENST00000685175.1 | protein_coding | 13/13 | 923 | chr17 | 76779275 |
| view | chr:pos | ref | alt | # # of ghapid:genebody level |
ghapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | genebody_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr17:76738516 | C | T | 301 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0010 others(298): Show |
314 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(311): Show |
intron_variant | MODIFIER | c.96+68C>T | MFSD11 | ENSG00000092931.12 | transcript | ENST00000685175.1 | protein_coding | 1/12 | chr17 | 76738516 | |||||||
| chr17:76738560 | T | C | 29 | a0001c0001t0001g0003 a0001c0001t0001g0044 a0001c0001t0001g0046 others(26): Show |
30 | HG00544.hp1 HG01070.hp2 HG01071.hp1 others(27): Show |
intron_variant | MODIFIER | c.96+112T>C | MFSD11 | ENSG00000092931.12 | transcript | ENST00000685175.1 | protein_coding | 1/12 | chr17 | 76738560 | |||||||
| chr17:76738569 | A | T | 4 | a0001c0001t0001g0332 a0001c0001t0001g0333 a0001c0001t0001g0334 others(1): Show |
4 | HG03098.hp2 HG03453.hp1 HG03516.hp1 others(1): Show |
intron_variant | MODIFIER | c.96+121A>T | MFSD11 | ENSG00000092931.12 | transcript | ENST00000685175.1 | protein_coding | 1/12 | chr17 | 76738569 | |||||||
| chr17:76738571 | A | G | 9 | a0001c0001t0003g0040 a0001c0001t0003g0041 a0001c0001t0005g0035 others(6): Show |
9 | HG01891.hp1 HG02602.hp1 HG02630.hp1 others(6): Show |
intron_variant | MODIFIER | c.96+123A>G | MFSD11 | ENSG00000092931.12 | transcript | ENST00000685175.1 | protein_coding | 1/12 | chr17 | 76738571 | |||||||
| chr17:76738572 | C | T | 1 | a0001c0001t0001g0331 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.96+124C>T | MFSD11 | ENSG00000092931.12 | transcript | ENST00000685175.1 | protein_coding | 1/12 | chr17 | 76738572 | |||||||
| chr17:76738575 | C | T | 4 | a0001c0001t0001g0332 a0001c0001t0001g0333 a0001c0001t0001g0334 others(1): Show |
4 | HG03098.hp2 HG03453.hp1 HG03516.hp1 others(1): Show |
intron_variant | MODIFIER | c.96+127C>T | MFSD11 | ENSG00000092931.12 | transcript | ENST00000685175.1 | protein_coding | 1/12 | chr17 | 76738575 | |||||||
| chr17:76738578 | C | T | 4 | a0001c0001t0001g0332 a0001c0001t0001g0333 a0001c0001t0001g0334 others(1): Show |
4 | HG03098.hp2 HG03453.hp1 HG03516.hp1 others(1): Show |
intron_variant | MODIFIER | c.96+130C>T | MFSD11 | ENSG00000092931.12 | transcript | ENST00000685175.1 | protein_coding | 1/12 | chr17 | 76738578 | |||||||
| chr17:76738619 | C | T | 2 | a0001c0006t0007g0042 a0001c0006t0007g0043 |
2 | HG02602.hp1 HG02735.hp1 |
intron_variant | MODIFIER | c.96+171C>T | MFSD11 | ENSG00000092931.12 | transcript | ENST00000685175.1 | protein_coding | 1/12 | chr17 | 76738619 | |||||||
| chr17:76738678 | C | T | 1 | a0001c0001t0001g0330 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.96+230C>T | MFSD11 | ENSG00000092931.12 | transcript | ENST00000685175.1 | protein_coding | 1/12 | chr17 | 76738678 | |||||||
| chr17:76738771 | C | T | 2 | a0001c0001t0001g0328 a0001c0001t0001g0329 |
2 | HG03209.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.97-167C>T | MFSD11 | ENSG00000092931.12 | transcript | ENST00000685175.1 | protein_coding | 1/12 | chr17 | 76738771 | |||||||
| chr17:76738829 | A | G | 1 | a0001c0001t0001g0335 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.97-109A>G | MFSD11 | ENSG00000092931.12 | transcript | ENST00000685175.1 | protein_coding | 1/12 | chr17 | 76738829 | |||||||
| chr17:76739006 | A | G | 4 | a0001c0001t0001g0324 a0001c0001t0001g0327 a0001c0001t0006g0325 others(1): Show |
4 | HG01099.hp1 HG01884.hp2 HG02572.hp2 others(1): Show |
intron_variant | MODIFIER | c.152+13A>G | MFSD11 | ENSG00000092931.12 | transcript | ENST00000685175.1 | protein_coding | 2/12 | chr17 | 76739006 | |||||||
| chr17:76739030 | A | G | 1 | a0001c0001t0001g0323 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.152+37A>G | MFSD11 | ENSG00000092931.12 | transcript | ENST00000685175.1 | protein_coding | 2/12 | chr17 | 76739030 | |||||||
| chr17:76739097 | G | A | 1 | a0001c0001t0009g0073 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.152+104G>A | MFSD11 | ENSG00000092931.12 | transcript | ENST00000685175.1 | protein_coding | 2/12 | chr17 | 76739097 | |||||||
| chr17:76739134 | A | G | 2 | a0001c0006t0007g0042 a0001c0006t0007g0043 |
2 | HG02602.hp1 HG02735.hp1 |
intron_variant | MODIFIER | c.152+141A>G | MFSD11 | ENSG00000092931.12 | transcript | ENST00000685175.1 | protein_coding | 2/12 | chr17 | 76739134 | |||||||
| chr17:76739260 | T | C | 16 | a0001c0001t0003g0011 a0001c0001t0003g0013 a0001c0001t0003g0014 others(13): Show |
16 | HG02258.hp1 HG02486.hp2 HG02559.hp1 others(13): Show |
intron_variant | MODIFIER | c.152+267T>C | MFSD11 | ENSG00000092931.12 | transcript | ENST00000685175.1 | protein_coding | 2/12 | chr17 | 76739260 | |||||||
| chr17:76739262 | C | T | 5 | a0001c0001t0004g0030 a0001c0001t0004g0031 a0001c0001t0004g0032 others(2): Show |
5 | HG01069.hp1 HG02258.hp2 HG02630.hp2 others(2): Show |
intron_variant | MODIFIER | c.152+269C>T | MFSD11 | ENSG00000092931.12 | transcript | ENST00000685175.1 | protein_coding | 2/12 | chr17 | 76739262 | |||||||
| chr17:76739276 | AAAGCACT others(4): Show |
A | 301 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0010 others(298): Show |
314 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(311): Show |
intron_variant | MODIFIER | c.152+285_152+295del others(11): Show |
MFSD11 | ENSG00000092931.12 | transcript | ENST00000685175.1 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr17 | 76739276 | ||||||
| chr17:76739359 | T | C | 1 | a0001c0001t0001g0044 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.152+366T>C | MFSD11 | ENSG00000092931.12 | transcript | ENST00000685175.1 | protein_coding | 2/12 | chr17 | 76739359 | |||||||
| chr17:76739380 | C | T | 1 | a0001c0001t0002g0322 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.152+387C>T | MFSD11 | ENSG00000092931.12 | transcript | ENST00000685175.1 | protein_coding | 2/12 | chr17 | 76739380 | |||||||
| chr17:76739448 | A | T | 2 | a0001c0006t0007g0042 a0001c0006t0007g0043 |
2 | HG02602.hp1 HG02735.hp1 |
intron_variant | MODIFIER | c.152+455A>T | MFSD11 | ENSG00000092931.12 | transcript | ENST00000685175.1 | protein_coding | 2/12 | chr17 | 76739448 | |||||||
| chr17:76739594 | A | G | 14 | a0001c0001t0003g0011 a0001c0001t0003g0013 a0001c0001t0003g0014 others(11): Show |
14 | HG02258.hp1 HG02486.hp2 HG02559.hp1 others(11): Show |
intron_variant | MODIFIER | c.152+601A>G | MFSD11 | ENSG00000092931.12 | transcript | ENST00000685175.1 | protein_coding | 2/12 | chr17 | 76739594 | |||||||
| chr17:76739884 | C | T | 1 | a0001c0001t0001g0003 | 2 | NA20752.hp1 NA20805.hp2 |
intron_variant | MODIFIER | c.152+891C>T | MFSD11 | ENSG00000092931.12 | transcript | ENST00000685175.1 | protein_coding | 2/12 | chr17 | 76739884 | |||||||
| chr17:76740010 | C | CA | 6 | a0001c0001t0002g0076 a0001c0001t0002g0077 a0001c0001t0003g0011 others(3): Show |
7 | HG01243.hp1 HG01884.hp1 HG02486.hp2 others(4): Show |
intron_variant | MODIFIER | c.153-933dupA | MFSD11 | ENSG00000092931.12 | transcript | ENST00000685175.1 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr17 | 76740010 | ||||||
| chr17:76740067 | G | T | 1 | a0001c0001t0001g0072 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.153-890G>T | MFSD11 | ENSG00000092931.12 | transcript | ENST00000685175.1 | protein_coding | 2/12 | chr17 | 76740067 | |||||||
| chr17:76740127 | TTG | T | 3 | a0001c0001t0001g0078 a0001c0001t0001g0079 a0001c0001t0001g0080 |
3 | HG02109.hp1 HG03225.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.153-827_153-826del others(2): Show |
MFSD11 | ENSG00000092931.12 | transcript | ENST00000685175.1 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr17 | 76740127 | ||||||
| chr17:76740173 | CA | C | 300 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0010 others(297): Show |
313 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(310): Show |
intron_variant | MODIFIER | c.153-764delA | MFSD11 | ENSG00000092931.12 | transcript | ENST00000685175.1 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr17 | 76740173 | ||||||
| chr17:76740410 | C | T | 1 | a0001c0001t0002g0071 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.153-547C>T | MFSD11 | ENSG00000092931.12 | transcript | ENST00000685175.1 | protein_coding | 2/12 | chr17 | 76740410 | |||||||
| chr17:76740603 | C | CTT | 14 | a0001c0001t0003g0011 a0001c0001t0003g0013 a0001c0001t0003g0014 others(11): Show |
14 | HG02258.hp1 HG02486.hp2 HG02559.hp1 others(11): Show |
intron_variant | MODIFIER | c.153-351_153-350dup others(2): Show |
MFSD11 | ENSG00000092931.12 | transcript | ENST00000685175.1 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr17 | 76740603 | ||||||
| chr17:76740619 | G | A | 3 | a0001c0002t0001g0004 a0001c0002t0001g0074 a0001c0002t0001g0075 |
4 | HG01243.hp1 HG01884.hp1 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.153-338G>A | MFSD11 | ENSG00000092931.12 | transcript | ENST00000685175.1 | protein_coding | 2/12 | chr17 | 76740619 | |||||||
| chr17:76740917 | C | CT | 25 | a0001c0001t0001g0101 a0001c0001t0001g0316 a0001c0001t0001g0318 others(22): Show |
25 | HG00735.hp1 HG00735.hp2 HG02056.hp2 others(22): Show |
intron_variant | MODIFIER | c.153-24dupT | MFSD11 | ENSG00000092931.12 | transcript | ENST00000685175.1 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr17 | 76740917 | ||||||
| chr17:76741119 | A | G | 2 | a0001c0006t0007g0042 a0001c0006t0007g0043 |
2 | HG02602.hp1 HG02735.hp1 |
intron_variant | MODIFIER | c.260+55A>G | MFSD11 | ENSG00000092931.12 | transcript | ENST00000685175.1 | protein_coding | 3/12 | chr17 | 76741119 | |||||||
| chr17:76741312 | A | G | 1 | a0001c0001t0002g0313 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.260+248A>G | MFSD11 | ENSG00000092931.12 | transcript | ENST00000685175.1 | protein_coding | 3/12 | chr17 | 76741312 | |||||||
| chr17:76741340 | A | C | 1 | a0001c0001t0001g0334 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.260+276A>C | MFSD11 | ENSG00000092931.12 | transcript | ENST00000685175.1 | protein_coding | 3/12 | chr17 | 76741340 | |||||||
| chr17:76741468 | G | A | 7 | a0001c0001t0001g0103 a0001c0001t0001g0105 a0001c0001t0001g0324 others(4): Show |
7 | HG00639.hp2 HG01099.hp1 HG01884.hp2 others(4): Show |
intron_variant | MODIFIER | c.260+404G>A | MFSD11 | ENSG00000092931.12 | transcript | ENST00000685175.1 | protein_coding | 3/12 | chr17 | 76741468 | |||||||
| chr17:76741718 | G | A | 1 | a0001c0001t0004g0030 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.261-251G>A | MFSD11 | ENSG00000092931.12 | transcript | ENST00000685175.1 | protein_coding | 3/12 | chr17 | 76741718 | |||||||
| chr17:76741888 | A | G | 1 | a0001c0001t0003g0024 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.261-81A>G | MFSD11 | ENSG00000092931.12 | transcript | ENST00000685175.1 | protein_coding | 3/12 | chr17 | 76741888 | |||||||
| chr17:76741933 | C | T | 1 | a0001c0001t0002g0312 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.261-36C>T | MFSD11 | ENSG00000092931.12 | transcript | ENST00000685175.1 | protein_coding | 3/12 | chr17 | 76741933 | |||||||
| chr17:76741934 | G | A | 14 | a0001c0001t0003g0011 a0001c0001t0003g0013 a0001c0001t0003g0014 others(11): Show |
14 | HG02258.hp1 HG02486.hp2 HG02559.hp1 others(11): Show |
intron_variant | MODIFIER | c.261-35G>A | MFSD11 | ENSG00000092931.12 | transcript | ENST00000685175.1 | protein_coding | 3/12 | chr17 | 76741934 | |||||||
| chr17:76742146 | T | G | 2 | a0001c0001t0005g0035 a0001c0001t0005g0036 |
2 | HG02886.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.341-31T>G | MFSD11 | ENSG00000092931.12 | transcript | ENST00000685175.1 | protein_coding | 4/12 | chr17 | 76742146 | |||||||
| chr17:76742326 | A | C | 16 | a0001c0001t0001g0298 a0001c0001t0001g0299 a0001c0001t0001g0300 others(13): Show |
16 | HG00558.hp2 HG00621.hp2 HG02074.hp1 others(13): Show |
intron_variant | MODIFIER | c.437+53A>C | MFSD11 | ENSG00000092931.12 | transcript | ENST00000685175.1 | protein_coding | 5/12 | chr17 | 76742326 | |||||||
| chr17:76742373 | C | T | 2 | a0001c0006t0007g0042 a0001c0006t0007g0043 |
2 | HG02602.hp1 HG02735.hp1 |
intron_variant | MODIFIER | c.437+100C>T | MFSD11 | ENSG00000092931.12 | transcript | ENST00000685175.1 | protein_coding | 5/12 | chr17 | 76742373 | |||||||
| chr17:76742501 | C | CT | 29 | a0001c0001t0001g0003 a0001c0001t0001g0044 a0001c0001t0001g0048 others(26): Show |
30 | HG00544.hp1 HG01070.hp2 HG01071.hp1 others(27): Show |
intron_variant | MODIFIER | c.437+243dupT | MFSD11 | ENSG00000092931.12 | transcript | ENST00000685175.1 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr17 | 76742501 | ||||||
| chr17:76742571 | C | T | 7 | a0001c0001t0003g0040 a0001c0001t0003g0041 a0001c0001t0005g0035 others(4): Show |
7 | HG01891.hp1 HG02630.hp1 HG02717.hp1 others(4): Show |
intron_variant | MODIFIER | c.437+298C>T | MFSD11 | ENSG00000092931.12 | transcript | ENST00000685175.1 | protein_coding | 5/12 | chr17 | 76742571 | |||||||
| chr17:76742575 | T | G | 38 | a0001c0001t0001g0087 a0001c0001t0001g0116 a0001c0001t0001g0117 others(35): Show |
41 | HG00140.hp2 HG00558.hp1 HG00609.hp1 others(38): Show |
intron_variant | MODIFIER | c.437+302T>G | MFSD11 | ENSG00000092931.12 | transcript | ENST00000685175.1 | protein_coding | 5/12 | chr17 | 76742575 | |||||||
| chr17:76742643 | C | A | 1 | a0001c0008t0001g0297 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.437+370C>A | MFSD11 | ENSG00000092931.12 | transcript | ENST00000685175.1 | protein_coding | 5/12 | chr17 | 76742643 | |||||||
| chr17:76742708 | G | C | 1 | a0001c0001t0001g0128 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.437+435G>C | MFSD11 | ENSG00000092931.12 | transcript | ENST00000685175.1 | protein_coding | 5/12 | chr17 | 76742708 | |||||||
| chr17:76742762 | C | T | 1 | a0001c0001t0001g0296 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.437+489C>T | MFSD11 | ENSG00000092931.12 | transcript | ENST00000685175.1 | protein_coding | 5/12 | chr17 | 76742762 | |||||||
| chr17:76743013 | A | G | 7 | a0001c0001t0002g0122 a0001c0001t0002g0123 a0001c0001t0002g0124 others(4): Show |
7 | NA18950.hp1 NA18952.hp2 NA18972.hp2 others(4): Show |
intron_variant | MODIFIER | c.438-385A>G | MFSD11 | ENSG00000092931.12 | transcript | ENST00000685175.1 | protein_coding | 5/12 | chr17 | 76743013 | |||||||
| chr17:76743015 | A | G | 3 | a0001c0002t0001g0004 a0001c0002t0001g0074 a0001c0002t0001g0075 |
4 | HG01243.hp1 HG01884.hp1 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.438-383A>G | MFSD11 | ENSG00000092931.12 | transcript | ENST00000685175.1 | protein_coding | 5/12 | chr17 | 76743015 | |||||||
| chr17:76743163 | C | G | 14 | a0001c0001t0003g0011 a0001c0001t0003g0013 a0001c0001t0003g0014 others(11): Show |
14 | HG02258.hp1 HG02486.hp2 HG02559.hp1 others(11): Show |
intron_variant | MODIFIER | c.438-235C>G | MFSD11 | ENSG00000092931.12 | transcript | ENST00000685175.1 | protein_coding | 5/12 | chr17 | 76743163 | |||||||
| chr17:76743343 | A | C | 1 | a0001c0001t0002g0295 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.438-55A>C | MFSD11 | ENSG00000092931.12 | transcript | ENST00000685175.1 | protein_coding | 5/12 | chr17 | 76743343 | |||||||
| chr17:76743524 | C | T | 1 | a0001c0001t0001g0335 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.496+68C>T | MFSD11 | ENSG00000092931.12 | transcript | ENST00000685175.1 | protein_coding | 6/12 | chr17 | 76743524 | |||||||
| chr17:76743550 | C | T | 1 | a0001c0001t0002g0294 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.496+94C>T | MFSD11 | ENSG00000092931.12 | transcript | ENST00000685175.1 | protein_coding | 6/12 | chr17 | 76743550 | |||||||
| chr17:76743762 | C | A | 1 | a0001c0001t0001g0129 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.496+306C>A | MFSD11 | ENSG00000092931.12 | transcript | ENST00000685175.1 | protein_coding | 6/12 | chr17 | 76743762 | |||||||
| chr17:76744019 | C | T | 1 | a0001c0001t0001g0329 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.497-303C>T | MFSD11 | ENSG00000092931.12 | transcript | ENST00000685175.1 | protein_coding | 6/12 | chr17 | 76744019 | |||||||
| chr17:76744098 | A | G | 7 | a0001c0001t0003g0040 a0001c0001t0003g0041 a0001c0001t0005g0035 others(4): Show |
7 | HG01891.hp1 HG02630.hp1 HG02717.hp1 others(4): Show |
intron_variant | MODIFIER | c.497-224A>G | MFSD11 | ENSG00000092931.12 | transcript | ENST00000685175.1 | protein_coding | 6/12 | chr17 | 76744098 | |||||||
| chr17:76744189 | G | C | 3 | a0001c0001t0003g0011 a0001c0001t0003g0014 a0001c0001t0004g0012 |
3 | HG02258.hp1 HG02486.hp2 HG02723.hp1 |
intron_variant | MODIFIER | c.497-133G>C | MFSD11 | ENSG00000092931.12 | transcript | ENST00000685175.1 | protein_coding | 6/12 | chr17 | 76744189 | |||||||
| chr17:76744318 | G | A | 15 | a0001c0001t0001g0324 a0001c0001t0003g0011 a0001c0001t0003g0013 others(12): Show |
15 | HG02258.hp1 HG02486.hp2 HG02559.hp1 others(12): Show |
splice_region_variant&intron_variant | LOW | c.497-4G>A | MFSD11 | ENSG00000092931.12 | transcript | ENST00000685175.1 | protein_coding | 6/12 | chr17 | 76744318 | |||||||
| chr17:76744575 | G | A | 3 | a0001c0001t0001g0130 a0001c0004t0001g0100 a0001c0004t0001g0131 |
3 | HG02145.hp2 NA18522.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.641+109G>A | MFSD11 | ENSG00000092931.12 | transcript | ENST00000685175.1 | protein_coding | 7/12 | chr17 | 76744575 | |||||||
| chr17:76744735 | A | G | 42 | a0001c0001t0001g0010 a0001c0001t0001g0097 a0001c0001t0001g0098 others(39): Show |
43 | HG00558.hp2 HG01069.hp2 HG01071.hp2 others(40): Show |
intron_variant | MODIFIER | c.641+269A>G | MFSD11 | ENSG00000092931.12 | transcript | ENST00000685175.1 | protein_coding | 7/12 | chr17 | 76744735 | |||||||
| chr17:76744743 | C | T | 1 | a0001c0001t0001g0070 | 1 | NA18991.hp2 | intron_variant | MODIFIER | c.641+277C>T | MFSD11 | ENSG00000092931.12 | transcript | ENST00000685175.1 | protein_coding | 7/12 | chr17 | 76744743 | |||||||
| chr17:76744909 | C | T | 14 | a0001c0001t0003g0011 a0001c0001t0003g0013 a0001c0001t0003g0014 others(11): Show |
14 | HG02258.hp1 HG02486.hp2 HG02559.hp1 others(11): Show |
intron_variant | MODIFIER | c.641+443C>T | MFSD11 | ENSG00000092931.12 | transcript | ENST00000685175.1 | protein_coding | 7/12 | chr17 | 76744909 | |||||||
| chr17:76744944 | G | A | 29 | a0001c0001t0001g0003 a0001c0001t0001g0044 a0001c0001t0001g0046 others(26): Show |
30 | HG00544.hp1 HG01070.hp2 HG01071.hp1 others(27): Show |
intron_variant | MODIFIER | c.641+478G>A | MFSD11 | ENSG00000092931.12 | transcript | ENST00000685175.1 | protein_coding | 7/12 | chr17 | 76744944 | |||||||
| chr17:76744946 | C | G | 1 | a0001c0001t0002g0271 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.641+480C>G | MFSD11 | ENSG00000092931.12 | transcript | ENST00000685175.1 | protein_coding | 7/12 | chr17 | 76744946 | |||||||
| chr17:76744964 | T | C | 1 | a0001c0001t0013g0132 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.641+498T>C | MFSD11 | ENSG00000092931.12 | transcript | ENST00000685175.1 | protein_coding | 7/12 | chr17 | 76744964 | |||||||
| chr17:76744968 | C | T | 14 | a0001c0001t0003g0011 a0001c0001t0003g0013 a0001c0001t0003g0014 others(11): Show |
14 | HG02258.hp1 HG02486.hp2 HG02559.hp1 others(11): Show |
intron_variant | MODIFIER | c.641+502C>T | MFSD11 | ENSG00000092931.12 | transcript | ENST00000685175.1 | protein_coding | 7/12 | chr17 | 76744968 | |||||||
| chr17:76745082 | A | G | 1 | a0001c0001t0001g0270 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.641+616A>G | MFSD11 | ENSG00000092931.12 | transcript | ENST00000685175.1 | protein_coding | 7/12 | chr17 | 76745082 | |||||||
| chr17:76745234 | G | C | 1 | a0001c0001t0001g0133 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.641+768G>C | MFSD11 | ENSG00000092931.12 | transcript | ENST00000685175.1 | protein_coding | 7/12 | chr17 | 76745234 | |||||||
| chr17:76745275 | A | G | 2 | a0001c0006t0007g0042 a0001c0006t0007g0043 |
2 | HG02602.hp1 HG02735.hp1 |
intron_variant | MODIFIER | c.641+809A>G | MFSD11 | ENSG00000092931.12 | transcript | ENST00000685175.1 | protein_coding | 7/12 | chr17 | 76745275 | |||||||
| chr17:76745437 | C | T | 14 | a0001c0001t0003g0011 a0001c0001t0003g0013 a0001c0001t0003g0014 others(11): Show |
14 | HG02258.hp1 HG02486.hp2 HG02559.hp1 others(11): Show |
intron_variant | MODIFIER | c.641+971C>T | MFSD11 | ENSG00000092931.12 | transcript | ENST00000685175.1 | protein_coding | 7/12 | chr17 | 76745437 | |||||||
| chr17:76745544 | T | C | 1 | a0001c0001t0001g0272 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.641+1078T>C | MFSD11 | ENSG00000092931.12 | transcript | ENST00000685175.1 | protein_coding | 7/12 | chr17 | 76745544 | |||||||
| chr17:76745745 | G | A | 2 | a0001c0006t0007g0042 a0001c0006t0007g0043 |
2 | HG02602.hp1 HG02735.hp1 |
intron_variant | MODIFIER | c.641+1279G>A | MFSD11 | ENSG00000092931.12 | transcript | ENST00000685175.1 | protein_coding | 7/12 | chr17 | 76745745 | |||||||
| chr17:76745749 | C | G | 1 | a0001c0001t0002g0091 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.641+1283C>G | MFSD11 | ENSG00000092931.12 | transcript | ENST00000685175.1 | protein_coding | 7/12 | chr17 | 76745749 | |||||||
| chr17:76745763 | A | G | 1 | a0001c0001t0001g0269 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.641+1297A>G | MFSD11 | ENSG00000092931.12 | transcript | ENST00000685175.1 | protein_coding | 7/12 | chr17 | 76745763 | |||||||
| chr17:76745804 | A | ATTAT | 3 | a0001c0001t0001g0047 a0001c0001t0001g0267 a0001c0001t0001g0268 |
3 | HG00597.hp1 NA18942.hp2 NA19062.hp2 |
intron_variant | MODIFIER | c.641+1342_641+1345d others(6): Show |
MFSD11 | ENSG00000092931.12 | transcript | ENST00000685175.1 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr17 | 76745804 | ||||||
| chr17:76745812 | C | CTTAT | 283 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0010 others(280): Show |
296 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(293): Show |
intron_variant | MODIFIER | c.641+1373_641+1376d others(6): Show |
MFSD11 | ENSG00000092931.12 | transcript | ENST00000685175.1 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr17 | 76745812 | ||||||
| chr17:76745812 | C | CTTATTTA others(1): Show |
31 | a0001c0001t0001g0048 a0001c0001t0001g0097 a0001c0001t0001g0103 others(28): Show |
31 | HG00544.hp1 HG00639.hp2 HG00735.hp2 others(28): Show |
intron_variant | MODIFIER | c.641+1369_641+1376d others(10): Show |
MFSD11 | ENSG00000092931.12 | transcript | ENST00000685175.1 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr17 | 76745812 | ||||||
| chr17:76745812 | C | CTTATTTA others(5): Show |
1 | a0001c0001t0001g0134 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.641+1365_641+1376d others(14): Show |
MFSD11 | ENSG00000092931.12 | transcript | ENST00000685175.1 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr17 | 76745812 | ||||||
| chr17:76745812 | C | T | 10 | a0001c0001t0001g0047 a0001c0001t0001g0267 a0001c0001t0001g0268 others(7): Show |
10 | HG00597.hp1 HG01891.hp1 HG02630.hp1 others(7): Show |
intron_variant | MODIFIER | c.641+1346C>T | MFSD11 | ENSG00000092931.12 | transcript | ENST00000685175.1 | protein_coding | 7/12 | chr17 | 76745812 | |||||||
| chr17:76745812 | CTTAT | C | 3 | a0001c0001t0001g0320 a0001c0006t0007g0042 a0001c0006t0007g0043 |
3 | HG02602.hp1 HG02735.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.641+1373_641+1376d others(6): Show |
MFSD11 | ENSG00000092931.12 | transcript | ENST00000685175.1 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr17 | 76745812 | ||||||
| chr17:76745847 | A | G | 1 | a0001c0001t0002g0266 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.641+1381A>G | MFSD11 | ENSG00000092931.12 | transcript | ENST00000685175.1 | protein_coding | 7/12 | chr17 | 76745847 | |||||||
| chr17:76745964 | G | C | 3 | a0001c0001t0001g0135 a0001c0001t0001g0136 a0001c0001t0001g0137 |
3 | HG02965.hp1 HG03130.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.641+1498G>C | MFSD11 | ENSG00000092931.12 | transcript | ENST00000685175.1 | protein_coding | 7/12 | chr17 | 76745964 | |||||||
| chr17:76746026 | G | C | 3 | a0001c0001t0002g0081 a0001c0001t0002g0106 a0001c0001t0002g0107 |
3 | HG02071.hp2 HG02080.hp1 HG02132.hp1 |
intron_variant | MODIFIER | c.641+1560G>C | MFSD11 | ENSG00000092931.12 | transcript | ENST00000685175.1 | protein_coding | 7/12 | chr17 | 76746026 | |||||||
| chr17:76746206 | T | G | 7 | a0001c0001t0003g0040 a0001c0001t0003g0041 a0001c0001t0005g0035 others(4): Show |
7 | HG01891.hp1 HG02630.hp1 HG02717.hp1 others(4): Show |
intron_variant | MODIFIER | c.641+1740T>G | MFSD11 | ENSG00000092931.12 | transcript | ENST00000685175.1 | protein_coding | 7/12 | chr17 | 76746206 | |||||||
| chr17:76746263 | C | T | 2 | a0001c0006t0007g0042 a0001c0006t0007g0043 |
2 | HG02602.hp1 HG02735.hp1 |
intron_variant | MODIFIER | c.641+1797C>T | MFSD11 | ENSG00000092931.12 | transcript | ENST00000685175.1 | protein_coding | 7/12 | chr17 | 76746263 | |||||||
| chr17:76746460 | A | G | 301 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0010 others(298): Show |
314 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(311): Show |
intron_variant | MODIFIER | c.641+1994A>G | MFSD11 | ENSG00000092931.12 | transcript | ENST00000685175.1 | protein_coding | 7/12 | chr17 | 76746460 | |||||||
| chr17:76746525 | C | T | 1 | a0001c0001t0002g0265 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.641+2059C>T | MFSD11 | ENSG00000092931.12 | transcript | ENST00000685175.1 | protein_coding | 7/12 | chr17 | 76746525 | |||||||
| chr17:76746627 | A | G | 2 | a0001c0001t0002g0120 a0001c0001t0002g0121 |
2 | HG03017.hp1 HG03704.hp1 |
intron_variant | MODIFIER | c.641+2161A>G | MFSD11 | ENSG00000092931.12 | transcript | ENST00000685175.1 | protein_coding | 7/12 | chr17 | 76746627 | |||||||
| chr17:76746659 | G | A | 1 | a0001c0001t0002g0082 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.641+2193G>A | MFSD11 | ENSG00000092931.12 | transcript | ENST00000685175.1 | protein_coding | 7/12 | chr17 | 76746659 | |||||||
| chr17:76746728 | C | T | 14 | a0001c0001t0003g0011 a0001c0001t0003g0013 a0001c0001t0003g0014 others(11): Show |
14 | HG02258.hp1 HG02486.hp2 HG02559.hp1 others(11): Show |
intron_variant | MODIFIER | c.641+2262C>T | MFSD11 | ENSG00000092931.12 | transcript | ENST00000685175.1 | protein_coding | 7/12 | chr17 | 76746728 | |||||||
| chr17:76746912 | CA | C | 5 | a0001c0001t0004g0030 a0001c0001t0004g0031 a0001c0001t0004g0032 others(2): Show |
5 | HG01069.hp1 HG02258.hp2 HG02630.hp2 others(2): Show |
intron_variant | MODIFIER | c.641+2447delA | MFSD11 | ENSG00000092931.12 | transcript | ENST00000685175.1 | protein_coding | 7/12 | chr17 | 76746912 | |||||||
| chr17:76747001 | C | T | 5 | a0001c0001t0004g0030 a0001c0001t0004g0031 a0001c0001t0004g0032 others(2): Show |
5 | HG01069.hp1 HG02258.hp2 HG02630.hp2 others(2): Show |
intron_variant | MODIFIER | c.641+2535C>T | MFSD11 | ENSG00000092931.12 | transcript | ENST00000685175.1 | protein_coding | 7/12 | chr17 | 76747001 | |||||||
| chr17:76747012 | G | A | 2 | a0001c0006t0007g0042 a0001c0006t0007g0043 |
2 | HG02602.hp1 HG02735.hp1 |
intron_variant | MODIFIER | c.641+2546G>A | MFSD11 | ENSG00000092931.12 | transcript | ENST00000685175.1 | protein_coding | 7/12 | chr17 | 76747012 | |||||||
| chr17:76747015 | TC | T | 28 | a0001c0001t0003g0011 a0001c0001t0003g0013 a0001c0001t0003g0014 others(25): Show |
28 | HG01069.hp1 HG01891.hp1 HG02258.hp1 others(25): Show |
intron_variant | MODIFIER | c.641+2551delC | MFSD11 | ENSG00000092931.12 | transcript | ENST00000685175.1 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr17 | 76747015 | ||||||
| chr17:76747116 | A | T | 3 | a0001c0001t0001g0262 a0001c0001t0001g0263 a0001c0001t0001g0264 |
3 | HG02080.hp2 HG03831.hp1 NA18980.hp1 |
intron_variant | MODIFIER | c.641+2650A>T | MFSD11 | ENSG00000092931.12 | transcript | ENST00000685175.1 | protein_coding | 7/12 | chr17 | 76747116 | |||||||
| chr17:76747327 | A | T | 1 | a0001c0001t0001g0261 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.641+2861A>T | MFSD11 | ENSG00000092931.12 | transcript | ENST00000685175.1 | protein_coding | 7/12 | chr17 | 76747327 | |||||||
| chr17:76747447 | G | A | 1 | a0001c0001t0002g0295 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.641+2981G>A | MFSD11 | ENSG00000092931.12 | transcript | ENST00000685175.1 | protein_coding | 7/12 | chr17 | 76747447 | |||||||
| chr17:76747496 | A | G | 329 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0010 others(326): Show |
342 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(339): Show |
intron_variant | MODIFIER | c.641+3030A>G | MFSD11 | ENSG00000092931.12 | transcript | ENST00000685175.1 | protein_coding | 7/12 | chr17 | 76747496 | |||||||
| chr17:76747581 | C | T | 2 | a0001c0006t0007g0042 a0001c0006t0007g0043 |
2 | HG02602.hp1 HG02735.hp1 |
intron_variant | MODIFIER | c.641+3115C>T | MFSD11 | ENSG00000092931.12 | transcript | ENST00000685175.1 | protein_coding | 7/12 | chr17 | 76747581 | |||||||
| chr17:76747622 | C | T | 11 | a0001c0001t0003g0013 a0001c0001t0003g0015 a0001c0001t0003g0016 others(8): Show |
11 | HG02559.hp1 HG02559.hp2 HG02615.hp1 others(8): Show |
intron_variant | MODIFIER | c.641+3156C>T | MFSD11 | ENSG00000092931.12 | transcript | ENST00000685175.1 | protein_coding | 7/12 | chr17 | 76747622 | |||||||
| chr17:76747624 | C | T | 3 | a0001c0001t0001g0290 a0001c0001t0001g0291 a0001c0001t0001g0292 |
3 | HG02809.hp1 HG02970.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.641+3158C>T | MFSD11 | ENSG00000092931.12 | transcript | ENST00000685175.1 | protein_coding | 7/12 | chr17 | 76747624 | |||||||
| chr17:76747685 | A | T | 12 | a0001c0001t0003g0040 a0001c0001t0003g0041 a0001c0001t0004g0030 others(9): Show |
12 | HG01069.hp1 HG01891.hp1 HG02258.hp2 others(9): Show |
intron_variant | MODIFIER | c.641+3219A>T | MFSD11 | ENSG00000092931.12 | transcript | ENST00000685175.1 | protein_coding | 7/12 | chr17 | 76747685 | |||||||
| chr17:76747769 | G | T | 1 | a0001c0001t0001g0260 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.641+3303G>T | MFSD11 | ENSG00000092931.12 | transcript | ENST00000685175.1 | protein_coding | 7/12 | chr17 | 76747769 | |||||||
| chr17:76747775 | C | T | 1 | a0001c0001t0003g0011 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.641+3309C>T | MFSD11 | ENSG00000092931.12 | transcript | ENST00000685175.1 | protein_coding | 7/12 | chr17 | 76747775 | |||||||
| chr17:76747839 | G | A | 1 | a0001c0001t0001g0146 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.641+3373G>A | MFSD11 | ENSG00000092931.12 | transcript | ENST00000685175.1 | protein_coding | 7/12 | chr17 | 76747839 | |||||||
| chr17:76748076 | G | T | 2 | a0001c0006t0007g0042 a0001c0006t0007g0043 |
2 | HG02602.hp1 HG02735.hp1 |
intron_variant | MODIFIER | c.641+3610G>T | MFSD11 | ENSG00000092931.12 | transcript | ENST00000685175.1 | protein_coding | 7/12 | chr17 | 76748076 | |||||||
| chr17:76748097 | T | TG | 18 | a0001c0001t0001g0048 a0001c0001t0001g0069 a0001c0001t0001g0070 others(15): Show |
18 | HG00544.hp1 HG00642.hp1 HG01192.hp1 others(15): Show |
intron_variant | MODIFIER | c.641+3638dupG | MFSD11 | ENSG00000092931.12 | transcript | ENST00000685175.1 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr17 | 76748097 | ||||||
| chr17:76748098 | G | A | 7 | a0001c0001t0003g0040 a0001c0001t0003g0041 a0001c0001t0005g0035 others(4): Show |
7 | HG01891.hp1 HG02630.hp1 HG02717.hp1 others(4): Show |
intron_variant | MODIFIER | c.641+3632G>A | MFSD11 | ENSG00000092931.12 | transcript | ENST00000685175.1 | protein_coding | 7/12 | chr17 | 76748098 | |||||||
| chr17:76748105 | A | G | 1 | a0001c0001t0011g0289 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.641+3639A>G | MFSD11 | ENSG00000092931.12 | transcript | ENST00000685175.1 | protein_coding | 7/12 | chr17 | 76748105 | |||||||
| chr17:76748106 | GGGGGGAG others(14): Show |
G | 7 | a0001c0001t0003g0040 a0001c0001t0003g0041 a0001c0001t0005g0035 others(4): Show |
7 | HG01891.hp1 HG02630.hp1 HG02717.hp1 others(4): Show |
intron_variant | MODIFIER | c.641+3641_641+3661d others(23): Show |
MFSD11 | ENSG00000092931.12 | transcript | ENST00000685175.1 | protein_coding | 7/12 | chr17 | 76748106 | |||||||
| chr17:76748368 | T | A | 15 | a0001c0001t0001g0103 a0001c0001t0001g0105 a0001c0001t0001g0129 others(12): Show |
15 | HG00639.hp2 HG01099.hp1 HG01884.hp2 others(12): Show |
intron_variant | MODIFIER | c.641+3902T>A | MFSD11 | ENSG00000092931.12 | transcript | ENST00000685175.1 | protein_coding | 7/12 | chr17 | 76748368 | |||||||
| chr17:76748370 | T | A | 14 | a0001c0001t0003g0011 a0001c0001t0003g0013 a0001c0001t0003g0014 others(11): Show |
14 | HG02258.hp1 HG02486.hp2 HG02559.hp1 others(11): Show |
intron_variant | MODIFIER | c.641+3904T>A | MFSD11 | ENSG00000092931.12 | transcript | ENST00000685175.1 | protein_coding | 7/12 | chr17 | 76748370 | |||||||
| chr17:76748467 | C | T | 14 | a0001c0001t0003g0011 a0001c0001t0003g0013 a0001c0001t0003g0014 others(11): Show |
14 | HG02258.hp1 HG02486.hp2 HG02559.hp1 others(11): Show |
intron_variant | MODIFIER | c.641+4001C>T | MFSD11 | ENSG00000092931.12 | transcript | ENST00000685175.1 | protein_coding | 7/12 | chr17 | 76748467 | |||||||
| chr17:76748626 | C | T | 1 | a0001c0001t0010g0090 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.641+4160C>T | MFSD11 | ENSG00000092931.12 | transcript | ENST00000685175.1 | protein_coding | 7/12 | chr17 | 76748626 | |||||||
| chr17:76748643 | G | A | 1 | a0001c0001t0001g0329 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.641+4177G>A | MFSD11 | ENSG00000092931.12 | transcript | ENST00000685175.1 | protein_coding | 7/12 | chr17 | 76748643 | |||||||
| chr17:76748719 | G | T | 10 | a0001c0001t0003g0013 a0001c0001t0003g0016 a0001c0001t0003g0017 others(7): Show |
10 | HG02559.hp1 HG02559.hp2 HG02615.hp1 others(7): Show |
intron_variant | MODIFIER | c.641+4253G>T | MFSD11 | ENSG00000092931.12 | transcript | ENST00000685175.1 | protein_coding | 7/12 | chr17 | 76748719 | |||||||
| chr17:76748725 | TG | T | 264 | a0001c0001t0001g0007 a0001c0001t0001g0010 a0001c0001t0001g0078 others(261): Show |
276 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(273): Show |
intron_variant | MODIFIER | c.641+4260delG | MFSD11 | ENSG00000092931.12 | transcript | ENST00000685175.1 | protein_coding | 7/12 | chr17 | 76748725 | |||||||
| chr17:76748743 | T | C | 1 | a0001c0001t0003g0016 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.641+4277T>C | MFSD11 | ENSG00000092931.12 | transcript | ENST00000685175.1 | protein_coding | 7/12 | chr17 | 76748743 | |||||||
| chr17:76748844 | T | A | 26 | a0001c0001t0001g0098 a0001c0001t0001g0278 a0001c0001t0001g0279 others(23): Show |
26 | HG00558.hp2 HG02074.hp1 HG02145.hp1 others(23): Show |
intron_variant | MODIFIER | c.641+4378T>A | MFSD11 | ENSG00000092931.12 | transcript | ENST00000685175.1 | protein_coding | 7/12 | chr17 | 76748844 | |||||||
| chr17:76748932 | C | T | 217 | a0001c0001t0001g0010 a0001c0001t0001g0087 a0001c0001t0001g0093 others(214): Show |
227 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(224): Show |
intron_variant | MODIFIER | c.641+4466C>T | MFSD11 | ENSG00000092931.12 | transcript | ENST00000685175.1 | protein_coding | 7/12 | chr17 | 76748932 | |||||||
| chr17:76749225 | G | C | 15 | a0001c0001t0001g0103 a0001c0001t0001g0105 a0001c0001t0001g0129 others(12): Show |
15 | HG00639.hp2 HG01099.hp1 HG01884.hp2 others(12): Show |
intron_variant | MODIFIER | c.641+4759G>C | MFSD11 | ENSG00000092931.12 | transcript | ENST00000685175.1 | protein_coding | 7/12 | chr17 | 76749225 | |||||||
| chr17:76749298 | C | T | 5 | a0001c0001t0001g0299 a0001c0001t0001g0306 a0001c0001t0001g0307 others(2): Show |
5 | NA18965.hp2 NA18971.hp2 NA19070.hp1 others(2): Show |
intron_variant | MODIFIER | c.642-4749C>T | MFSD11 | ENSG00000092931.12 | transcript | ENST00000685175.1 | protein_coding | 7/12 | chr17 | 76749298 | |||||||
| chr17:76749443 | C | T | 2 | a0001c0006t0007g0042 a0001c0006t0007g0043 |
2 | HG02602.hp1 HG02735.hp1 |
intron_variant | MODIFIER | c.642-4604C>T | MFSD11 | ENSG00000092931.12 | transcript | ENST00000685175.1 | protein_coding | 7/12 | chr17 | 76749443 | |||||||
| chr17:76749458 | C | T | 2 | a0001c0001t0003g0013 a0001c0001t0003g0023 |
2 | NA18959.hp2 NA19075.hp2 |
intron_variant | MODIFIER | c.642-4589C>T | MFSD11 | ENSG00000092931.12 | transcript | ENST00000685175.1 | protein_coding | 7/12 | chr17 | 76749458 | |||||||
| chr17:76749472 | T | C | 1 | a0001c0001t0001g0179 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.642-4575T>C | MFSD11 | ENSG00000092931.12 | transcript | ENST00000685175.1 | protein_coding | 7/12 | chr17 | 76749472 | |||||||
| chr17:76749495 | A | G | 1 | a0001c0001t0002g0091 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.642-4552A>G | MFSD11 | ENSG00000092931.12 | transcript | ENST00000685175.1 | protein_coding | 7/12 | chr17 | 76749495 | |||||||
| chr17:76749531 | C | CA | 321 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0010 others(318): Show |
334 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(331): Show |
intron_variant | MODIFIER | c.642-4505dupA | MFSD11 | ENSG00000092931.12 | transcript | ENST00000685175.1 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr17 | 76749531 | ||||||
| chr17:76749531 | C | CAA | 7 | a0001c0001t0002g0180 a0001c0001t0002g0181 a0001c0001t0002g0182 others(4): Show |
7 | HG02071.hp1 HG02083.hp1 HG02602.hp1 others(4): Show |
intron_variant | MODIFIER | c.642-4506_642-4505d others(4): Show |
MFSD11 | ENSG00000092931.12 | transcript | ENST00000685175.1 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr17 | 76749531 | ||||||
| chr17:76749556 | C | T | 2 | a0001c0006t0007g0042 a0001c0006t0007g0043 |
2 | HG02602.hp1 HG02735.hp1 |
intron_variant | MODIFIER | c.642-4491C>T | MFSD11 | ENSG00000092931.12 | transcript | ENST00000685175.1 | protein_coding | 7/12 | chr17 | 76749556 | |||||||
| chr17:76749561 | T | A | 2 | a0001c0006t0007g0042 a0001c0006t0007g0043 |
2 | HG02602.hp1 HG02735.hp1 |
intron_variant | MODIFIER | c.642-4486T>A | MFSD11 | ENSG00000092931.12 | transcript | ENST00000685175.1 | protein_coding | 7/12 | chr17 | 76749561 | |||||||
| chr17:76749566 | T | C | 1 | a0001c0001t0001g0141 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.642-4481T>C | MFSD11 | ENSG00000092931.12 | transcript | ENST00000685175.1 | protein_coding | 7/12 | chr17 | 76749566 | |||||||
| chr17:76749571 | C | G | 299 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0010 others(296): Show |
311 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(308): Show |
intron_variant | MODIFIER | c.642-4476C>G | MFSD11 | ENSG00000092931.12 | transcript | ENST00000685175.1 | protein_coding | 7/12 | chr17 | 76749571 | |||||||
| chr17:76749666 | C | T | 1 | a0001c0001t0003g0041 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.642-4381C>T | MFSD11 | ENSG00000092931.12 | transcript | ENST00000685175.1 | protein_coding | 7/12 | chr17 | 76749666 | |||||||
| chr17:76749707 | T | G | 4 | a0001c0001t0001g0093 a0001c0001t0001g0135 a0001c0001t0001g0136 others(1): Show |
4 | HG02055.hp2 HG02965.hp1 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.642-4340T>G | MFSD11 | ENSG00000092931.12 | transcript | ENST00000685175.1 | protein_coding | 7/12 | chr17 | 76749707 | |||||||
| chr17:76749848 | C | T | 1 | a0001c0001t0001g0070 | 1 | NA18991.hp2 | intron_variant | MODIFIER | c.642-4199C>T | MFSD11 | ENSG00000092931.12 | transcript | ENST00000685175.1 | protein_coding | 7/12 | chr17 | 76749848 | |||||||
| chr17:76749889 | C | CA | 9 | a0001c0001t0001g0098 a0001c0001t0001g0150 a0001c0001t0001g0257 others(6): Show |
9 | HG00733.hp2 HG01978.hp2 HG04184.hp2 others(6): Show |
intron_variant | MODIFIER | c.642-4141dupA | MFSD11 | ENSG00000092931.12 | transcript | ENST00000685175.1 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr17 | 76749889 | ||||||
| chr17:76749889 | CA | C | 21 | a0001c0001t0001g0252 a0001c0001t0002g0253 a0001c0001t0003g0011 others(18): Show |
21 | HG01069.hp1 HG01891.hp1 HG02258.hp1 others(18): Show |
intron_variant | MODIFIER | c.642-4141delA | MFSD11 | ENSG00000092931.12 | transcript | ENST00000685175.1 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr17 | 76749889 | ||||||
| chr17:76749940 | G | A | 1 | a0001c0001t0002g0118 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.642-4107G>A | MFSD11 | ENSG00000092931.12 | transcript | ENST00000685175.1 | protein_coding | 7/12 | chr17 | 76749940 | |||||||
| chr17:76750123 | T | C | 3 | a0001c0001t0003g0017 a0001c0001t0003g0018 a0001c0001t0003g0040 |
3 | HG01891.hp1 HG02559.hp2 HG02615.hp1 |
intron_variant | MODIFIER | c.642-3924T>C | MFSD11 | ENSG00000092931.12 | transcript | ENST00000685175.1 | protein_coding | 7/12 | chr17 | 76750123 | |||||||
| chr17:76750148 | T | C | 2 | a0001c0001t0002g0049 a0001c0001t0002g0071 |
2 | HG02074.hp2 NA18943.hp2 |
intron_variant | MODIFIER | c.642-3899T>C | MFSD11 | ENSG00000092931.12 | transcript | ENST00000685175.1 | protein_coding | 7/12 | chr17 | 76750148 | |||||||
| chr17:76750266 | A | G | 328 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0010 others(325): Show |
341 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(338): Show |
intron_variant | MODIFIER | c.642-3781A>G | MFSD11 | ENSG00000092931.12 | transcript | ENST00000685175.1 | protein_coding | 7/12 | chr17 | 76750266 | |||||||
| chr17:76750287 | G | T | 5 | a0001c0001t0004g0030 a0001c0001t0004g0031 a0001c0001t0004g0032 others(2): Show |
5 | HG01069.hp1 HG02258.hp2 HG02630.hp2 others(2): Show |
intron_variant | MODIFIER | c.642-3760G>T | MFSD11 | ENSG00000092931.12 | transcript | ENST00000685175.1 | protein_coding | 7/12 | chr17 | 76750287 | |||||||
| chr17:76750326 | T | A | 1 | a0001c0001t0003g0015 | 1 | NA18947.hp1 | intron_variant | MODIFIER | c.642-3721T>A | MFSD11 | ENSG00000092931.12 | transcript | ENST00000685175.1 | protein_coding | 7/12 | chr17 | 76750326 | |||||||
| chr17:76750343 | C | T | 99 | a0001c0001t0001g0101 a0001c0001t0001g0117 a0001c0001t0001g0133 others(96): Show |
104 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(101): Show |
intron_variant | MODIFIER | c.642-3704C>T | MFSD11 | ENSG00000092931.12 | transcript | ENST00000685175.1 | protein_coding | 7/12 | chr17 | 76750343 | |||||||
| chr17:76750364 | A | AT | 90 | a0001c0001t0001g0007 a0001c0001t0001g0010 a0001c0001t0001g0065 others(87): Show |
93 | HG00423.hp2 HG00558.hp2 HG00642.hp2 others(90): Show |
intron_variant | MODIFIER | c.642-3661dupT | MFSD11 | ENSG00000092931.12 | transcript | ENST00000685175.1 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr17 | 76750364 | ||||||
| chr17:76750364 | A | ATT | 8 | a0001c0001t0001g0099 a0001c0001t0001g0251 a0001c0001t0001g0287 others(5): Show |
8 | HG02074.hp1 HG02559.hp2 HG02647.hp2 others(5): Show |
intron_variant | MODIFIER | c.642-3662_642-3661d others(4): Show |
MFSD11 | ENSG00000092931.12 | transcript | ENST00000685175.1 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr17 | 76750364 | ||||||
| chr17:76750399 | C | T | 1 | a0001c0001t0001g0244 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.642-3648C>T | MFSD11 | ENSG00000092931.12 | transcript | ENST00000685175.1 | protein_coding | 7/12 | chr17 | 76750399 | |||||||
| chr17:76750443 | C | T | 1 | a0001c0001t0001g0141 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.642-3604C>T | MFSD11 | ENSG00000092931.12 | transcript | ENST00000685175.1 | protein_coding | 7/12 | chr17 | 76750443 | |||||||
| chr17:76750517 | C | T | 4 | a0001c0001t0001g0046 a0001c0001t0001g0064 a0001c0001t0001g0068 others(1): Show |
4 | NA18974.hp2 NA18991.hp2 NA19011.hp2 others(1): Show |
intron_variant | MODIFIER | c.642-3530C>T | MFSD11 | ENSG00000092931.12 | transcript | ENST00000685175.1 | protein_coding | 7/12 | chr17 | 76750517 | |||||||
| chr17:76750578 | G | C | 4 | a0001c0001t0001g0129 a0001c0001t0001g0147 a0001c0001t0001g0148 others(1): Show |
4 | HG01891.hp2 HG02622.hp1 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.642-3469G>C | MFSD11 | ENSG00000092931.12 | transcript | ENST00000685175.1 | protein_coding | 7/12 | chr17 | 76750578 | |||||||
| chr17:76750622 | C | T | 1 | a0001c0001t0004g0012 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.642-3425C>T | MFSD11 | ENSG00000092931.12 | transcript | ENST00000685175.1 | protein_coding | 7/12 | chr17 | 76750622 | |||||||
| chr17:76750738 | C | CT | 15 | a0001c0001t0003g0011 a0001c0001t0003g0013 a0001c0001t0003g0014 others(12): Show |
15 | HG01891.hp1 HG02258.hp1 HG02486.hp2 others(12): Show |
intron_variant | MODIFIER | c.642-3301dupT | MFSD11 | ENSG00000092931.12 | transcript | ENST00000685175.1 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr17 | 76750738 | ||||||
| chr17:76750889 | C | T | 4 | a0001c0001t0001g0129 a0001c0001t0001g0147 a0001c0001t0001g0148 others(1): Show |
4 | HG01891.hp2 HG02622.hp1 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.642-3158C>T | MFSD11 | ENSG00000092931.12 | transcript | ENST00000685175.1 | protein_coding | 7/12 | chr17 | 76750889 | |||||||
| chr17:76750917 | C | T | 4 | a0001c0001t0001g0242 a0001c0001t0001g0243 a0001c0001t0001g0250 others(1): Show |
4 | HG00423.hp2 NA18960.hp2 NA18990.hp2 others(1): Show |
intron_variant | MODIFIER | c.642-3130C>T | MFSD11 | ENSG00000092931.12 | transcript | ENST00000685175.1 | protein_coding | 7/12 | chr17 | 76750917 | |||||||
| chr17:76750921 | G | A | 5 | a0001c0001t0005g0035 a0001c0001t0005g0036 a0001c0001t0005g0037 others(2): Show |
5 | HG02630.hp1 HG02886.hp2 HG03209.hp1 others(2): Show |
intron_variant | MODIFIER | c.642-3126G>A | MFSD11 | ENSG00000092931.12 | transcript | ENST00000685175.1 | protein_coding | 7/12 | chr17 | 76750921 | |||||||
| chr17:76750935 | C | G | 2 | a0001c0001t0001g0116 a0001c0001t0002g0115 |
2 | HG01361.hp2 HG02698.hp2 |
intron_variant | MODIFIER | c.642-3112C>G | MFSD11 | ENSG00000092931.12 | transcript | ENST00000685175.1 | protein_coding | 7/12 | chr17 | 76750935 | |||||||
| chr17:76750956 | A | C | 1 | a0001c0001t0004g0012 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.642-3091A>C | MFSD11 | ENSG00000092931.12 | transcript | ENST00000685175.1 | protein_coding | 7/12 | chr17 | 76750956 | |||||||
| chr17:76751119 | A | G | 324 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0010 others(321): Show |
337 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(334): Show |
intron_variant | MODIFIER | c.642-2928A>G | MFSD11 | ENSG00000092931.12 | transcript | ENST00000685175.1 | protein_coding | 7/12 | chr17 | 76751119 | |||||||
| chr17:76751138 | C | T | 1 | a0001c0001t0002g0241 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.642-2909C>T | MFSD11 | ENSG00000092931.12 | transcript | ENST00000685175.1 | protein_coding | 7/12 | chr17 | 76751138 | |||||||
| chr17:76751187 | G | A | 1 | a0001c0001t0001g0333 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.642-2860G>A | MFSD11 | ENSG00000092931.12 | transcript | ENST00000685175.1 | protein_coding | 7/12 | chr17 | 76751187 | |||||||
| chr17:76751239 | A | C | 1 | a0001c0001t0002g0077 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.642-2808A>C | MFSD11 | ENSG00000092931.12 | transcript | ENST00000685175.1 | protein_coding | 7/12 | chr17 | 76751239 | |||||||
| chr17:76751471 | A | G | 1 | a0001c0001t0003g0014 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.642-2576A>G | MFSD11 | ENSG00000092931.12 | transcript | ENST00000685175.1 | protein_coding | 7/12 | chr17 | 76751471 | |||||||
| chr17:76751541 | T | TCATGCCT others(21): Show |
2 | a0001c0006t0007g0042 a0001c0006t0007g0043 |
2 | HG02602.hp1 HG02735.hp1 |
intron_variant | MODIFIER | c.642-2496_642-2469d others(30): Show |
MFSD11 | ENSG00000092931.12 | transcript | ENST00000685175.1 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr17 | 76751541 | ||||||
| chr17:76751543 | A | G | 3 | a0001c0002t0001g0004 a0001c0002t0001g0074 a0001c0002t0001g0075 |
4 | HG01243.hp1 HG01884.hp1 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.642-2504A>G | MFSD11 | ENSG00000092931.12 | transcript | ENST00000685175.1 | protein_coding | 7/12 | chr17 | 76751543 | |||||||
| chr17:76751818 | A | G | 5 | a0001c0001t0004g0030 a0001c0001t0004g0031 a0001c0001t0004g0032 others(2): Show |
5 | HG01069.hp1 HG02258.hp2 HG02630.hp2 others(2): Show |
intron_variant | MODIFIER | c.642-2229A>G | MFSD11 | ENSG00000092931.12 | transcript | ENST00000685175.1 | protein_coding | 7/12 | chr17 | 76751818 | |||||||
| chr17:76751938 | C | T | 2 | a0001c0006t0007g0042 a0001c0006t0007g0043 |
2 | HG02602.hp1 HG02735.hp1 |
intron_variant | MODIFIER | c.642-2109C>T | MFSD11 | ENSG00000092931.12 | transcript | ENST00000685175.1 | protein_coding | 7/12 | chr17 | 76751938 | |||||||
| chr17:76752077 | G | T | 7 | a0001c0001t0001g0188 a0001c0001t0001g0252 a0001c0001t0001g0257 others(4): Show |
7 | HG00621.hp2 HG02615.hp2 HG02896.hp2 others(4): Show |
intron_variant | MODIFIER | c.642-1970G>T | MFSD11 | ENSG00000092931.12 | transcript | ENST00000685175.1 | protein_coding | 7/12 | chr17 | 76752077 | |||||||
| chr17:76752138 | A | G | 1 | a0001c0001t0002g0240 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.642-1909A>G | MFSD11 | ENSG00000092931.12 | transcript | ENST00000685175.1 | protein_coding | 7/12 | chr17 | 76752138 | |||||||
| chr17:76752153 | G | C | 4 | a0001c0001t0001g0332 a0001c0001t0001g0333 a0001c0001t0001g0334 others(1): Show |
4 | HG03098.hp2 HG03453.hp1 HG03516.hp1 others(1): Show |
intron_variant | MODIFIER | c.642-1894G>C | MFSD11 | ENSG00000092931.12 | transcript | ENST00000685175.1 | protein_coding | 7/12 | chr17 | 76752153 | |||||||
| chr17:76752160 | G | T | 1 | a0001c0001t0001g0093 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.642-1887G>T | MFSD11 | ENSG00000092931.12 | transcript | ENST00000685175.1 | protein_coding | 7/12 | chr17 | 76752160 | |||||||
| chr17:76752195 | G | A | 2 | a0001c0006t0007g0042 a0001c0006t0007g0043 |
2 | HG02602.hp1 HG02735.hp1 |
intron_variant | MODIFIER | c.642-1852G>A | MFSD11 | ENSG00000092931.12 | transcript | ENST00000685175.1 | protein_coding | 7/12 | chr17 | 76752195 | |||||||
| chr17:76752247 | T | C | 27 | a0001c0001t0001g0003 a0001c0001t0001g0044 a0001c0001t0001g0046 others(24): Show |
28 | HG00544.hp1 HG00735.hp2 HG01074.hp2 others(25): Show |
intron_variant | MODIFIER | c.642-1800T>C | MFSD11 | ENSG00000092931.12 | transcript | ENST00000685175.1 | protein_coding | 7/12 | chr17 | 76752247 | |||||||
| chr17:76752315 | A | T | 2 | a0001c0006t0007g0042 a0001c0006t0007g0043 |
2 | HG02602.hp1 HG02735.hp1 |
intron_variant | MODIFIER | c.642-1732A>T | MFSD11 | ENSG00000092931.12 | transcript | ENST00000685175.1 | protein_coding | 7/12 | chr17 | 76752315 | |||||||
| chr17:76752397 | A | AT | 12 | a0001c0001t0001g0133 a0001c0001t0001g0174 a0001c0001t0001g0175 others(9): Show |
12 | HG00642.hp1 HG01099.hp2 HG01192.hp2 others(9): Show |
intron_variant | MODIFIER | c.642-1633dupT | MFSD11 | ENSG00000092931.12 | transcript | ENST00000685175.1 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr17 | 76752397 | ||||||
| chr17:76752461 | A | G | 1 | a0001c0001t0002g0294 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.642-1586A>G | MFSD11 | ENSG00000092931.12 | transcript | ENST00000685175.1 | protein_coding | 7/12 | chr17 | 76752461 | |||||||
| chr17:76752483 | G | A | 8 | a0001c0001t0001g0151 a0001c0001t0001g0152 a0001c0001t0001g0153 others(5): Show |
8 | HG00639.hp1 HG00642.hp1 HG00741.hp2 others(5): Show |
intron_variant | MODIFIER | c.642-1564G>A | MFSD11 | ENSG00000092931.12 | transcript | ENST00000685175.1 | protein_coding | 7/12 | chr17 | 76752483 | |||||||
| chr17:76752578 | G | A | 27 | a0001c0001t0001g0003 a0001c0001t0001g0044 a0001c0001t0001g0046 others(24): Show |
28 | HG00544.hp1 HG00735.hp2 HG01074.hp2 others(25): Show |
intron_variant | MODIFIER | c.642-1469G>A | MFSD11 | ENSG00000092931.12 | transcript | ENST00000685175.1 | protein_coding | 7/12 | chr17 | 76752578 | |||||||
| chr17:76752659 | G | A | 1 | a0001c0001t0001g0155 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.642-1388G>A | MFSD11 | ENSG00000092931.12 | transcript | ENST00000685175.1 | protein_coding | 7/12 | chr17 | 76752659 | |||||||
| chr17:76752667 | G | A | 2 | a0001c0006t0007g0042 a0001c0006t0007g0043 |
2 | HG02602.hp1 HG02735.hp1 |
intron_variant | MODIFIER | c.642-1380G>A | MFSD11 | ENSG00000092931.12 | transcript | ENST00000685175.1 | protein_coding | 7/12 | chr17 | 76752667 | |||||||
| chr17:76752675 | C | T | 2 | a0001c0006t0007g0042 a0001c0006t0007g0043 |
2 | HG02602.hp1 HG02735.hp1 |
intron_variant | MODIFIER | c.642-1372C>T | MFSD11 | ENSG00000092931.12 | transcript | ENST00000685175.1 | protein_coding | 7/12 | chr17 | 76752675 | |||||||
| chr17:76752676 | G | A | 2 | a0001c0001t0002g0190 a0001c0001t0002g0191 |
2 | NA18948.hp2 NA18969.hp2 |
intron_variant | MODIFIER | c.642-1371G>A | MFSD11 | ENSG00000092931.12 | transcript | ENST00000685175.1 | protein_coding | 7/12 | chr17 | 76752676 | |||||||
| chr17:76752762 | C | A | 1 | a0001c0001t0001g0189 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.642-1285C>A | MFSD11 | ENSG00000092931.12 | transcript | ENST00000685175.1 | protein_coding | 7/12 | chr17 | 76752762 | |||||||
| chr17:76753035 | T | TA | 327 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0010 others(324): Show |
339 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(336): Show |
intron_variant | MODIFIER | c.642-1000dupA | MFSD11 | ENSG00000092931.12 | transcript | ENST00000685175.1 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr17 | 76753035 | ||||||
| chr17:76753191 | C | T | 23 | a0001c0001t0001g0178 a0001c0001t0001g0224 a0001c0001t0001g0225 others(20): Show |
23 | HG00099.hp2 HG00323.hp2 HG00642.hp2 others(20): Show |
intron_variant | MODIFIER | c.642-856C>T | MFSD11 | ENSG00000092931.12 | transcript | ENST00000685175.1 | protein_coding | 7/12 | chr17 | 76753191 | |||||||
| chr17:76753265 | C | CCT | 23 | a0001c0001t0003g0011 a0001c0001t0003g0013 a0001c0001t0003g0014 others(20): Show |
23 | HG01891.hp1 HG02258.hp1 HG02486.hp2 others(20): Show |
intron_variant | MODIFIER | c.642-780_642-779dup others(2): Show |
MFSD11 | ENSG00000092931.12 | transcript | ENST00000685175.1 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr17 | 76753265 | ||||||
| chr17:76753587 | G | A | 12 | a0001c0001t0003g0013 a0001c0001t0003g0016 a0001c0001t0003g0017 others(9): Show |
12 | HG01891.hp1 HG02559.hp1 HG02559.hp2 others(9): Show |
intron_variant | MODIFIER | c.642-460G>A | MFSD11 | ENSG00000092931.12 | transcript | ENST00000685175.1 | protein_coding | 7/12 | chr17 | 76753587 | |||||||
| chr17:76753614 | C | T | 3 | a0001c0001t0001g0290 a0001c0001t0001g0291 a0001c0001t0001g0292 |
3 | HG02809.hp1 HG02970.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.642-433C>T | MFSD11 | ENSG00000092931.12 | transcript | ENST00000685175.1 | protein_coding | 7/12 | chr17 | 76753614 | |||||||
| chr17:76753670 | G | A | 1 | a0001c0001t0002g0295 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.642-377G>A | MFSD11 | ENSG00000092931.12 | transcript | ENST00000685175.1 | protein_coding | 7/12 | chr17 | 76753670 | |||||||
| chr17:76753687 | C | CA | 311 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0010 others(308): Show |
323 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(320): Show |
intron_variant | MODIFIER | c.642-344dupA | MFSD11 | ENSG00000092931.12 | transcript | ENST00000685175.1 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr17 | 76753687 | ||||||
| chr17:76753687 | C | CAA | 7 | a0001c0001t0001g0150 a0001c0001t0001g0156 a0001c0001t0001g0290 others(4): Show |
8 | HG00280.hp1 HG00733.hp2 HG01243.hp1 others(5): Show |
intron_variant | MODIFIER | c.642-345_642-344dup others(2): Show |
MFSD11 | ENSG00000092931.12 | transcript | ENST00000685175.1 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr17 | 76753687 | ||||||
| chr17:76753817 | A | G | 5 | a0001c0001t0004g0030 a0001c0001t0004g0031 a0001c0001t0004g0032 others(2): Show |
5 | HG01069.hp1 HG02258.hp2 HG02630.hp2 others(2): Show |
intron_variant | MODIFIER | c.642-230A>G | MFSD11 | ENSG00000092931.12 | transcript | ENST00000685175.1 | protein_coding | 7/12 | chr17 | 76753817 | |||||||
| chr17:76753864 | A | C | 2 | a0001c0006t0007g0042 a0001c0006t0007g0043 |
2 | HG02602.hp1 HG02735.hp1 |
intron_variant | MODIFIER | c.642-183A>C | MFSD11 | ENSG00000092931.12 | transcript | ENST00000685175.1 | protein_coding | 7/12 | chr17 | 76753864 | |||||||
| chr17:76753916 | G | A | 15 | a0001c0001t0001g0103 a0001c0001t0001g0105 a0001c0001t0001g0129 others(12): Show |
15 | HG00639.hp2 HG01099.hp1 HG01884.hp2 others(12): Show |
intron_variant | MODIFIER | c.642-131G>A | MFSD11 | ENSG00000092931.12 | transcript | ENST00000685175.1 | protein_coding | 7/12 | chr17 | 76753916 | |||||||
| chr17:76753921 | A | C | 2 | a0001c0006t0007g0042 a0001c0006t0007g0043 |
2 | HG02602.hp1 HG02735.hp1 |
intron_variant | MODIFIER | c.642-126A>C | MFSD11 | ENSG00000092931.12 | transcript | ENST00000685175.1 | protein_coding | 7/12 | chr17 | 76753921 | |||||||
| chr17:76753963 | C | T | 6 | a0001c0001t0001g0097 a0001c0001t0001g0274 a0001c0001t0001g0275 others(3): Show |
6 | HG01069.hp2 HG01071.hp2 HG02622.hp2 others(3): Show |
intron_variant | MODIFIER | c.642-84C>T | MFSD11 | ENSG00000092931.12 | transcript | ENST00000685175.1 | protein_coding | 7/12 | chr17 | 76753963 | |||||||
| chr17:76754133 | C | CT | 329 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0010 others(326): Show |
342 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(339): Show |
intron_variant | MODIFIER | c.682+47dupT | MFSD11 | ENSG00000092931.12 | transcript | ENST00000685175.1 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr17 | 76754133 | ||||||
| chr17:76754249 | C | T | 302 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0010 others(299): Show |
315 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(312): Show |
intron_variant | MODIFIER | c.682+162C>T | MFSD11 | ENSG00000092931.12 | transcript | ENST00000685175.1 | protein_coding | 8/12 | chr17 | 76754249 | |||||||
| chr17:76754406 | C | T | 1 | a0001c0001t0001g0239 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.682+319C>T | MFSD11 | ENSG00000092931.12 | transcript | ENST00000685175.1 | protein_coding | 8/12 | chr17 | 76754406 | |||||||
| chr17:76754411 | A | G | 1 | a0001c0001t0001g0303 | 1 | NA19064.hp2 | intron_variant | MODIFIER | c.682+324A>G | MFSD11 | ENSG00000092931.12 | transcript | ENST00000685175.1 | protein_coding | 8/12 | chr17 | 76754411 | |||||||
| chr17:76754419 | G | A | 329 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0010 others(326): Show |
342 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(339): Show |
intron_variant | MODIFIER | c.682+332G>A | MFSD11 | ENSG00000092931.12 | transcript | ENST00000685175.1 | protein_coding | 8/12 | chr17 | 76754419 | |||||||
| chr17:76754510 | T | G | 1 | a0001c0001t0005g0035 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.682+423T>G | MFSD11 | ENSG00000092931.12 | transcript | ENST00000685175.1 | protein_coding | 8/12 | chr17 | 76754510 | |||||||
| chr17:76754683 | C | CA | 37 | a0001c0001t0001g0003 a0001c0001t0001g0044 a0001c0001t0001g0046 others(34): Show |
38 | HG00544.hp1 HG00735.hp2 HG01074.hp2 others(35): Show |
intron_variant | MODIFIER | c.682+612dupA | MFSD11 | ENSG00000092931.12 | transcript | ENST00000685175.1 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr17 | 76754683 | ||||||
| chr17:76754683 | C | CAA | 279 | a0001c0001t0001g0007 a0001c0001t0001g0010 a0001c0001t0001g0069 others(276): Show |
291 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(288): Show |
intron_variant | MODIFIER | c.682+611_682+612dup others(2): Show |
MFSD11 | ENSG00000092931.12 | transcript | ENST00000685175.1 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr17 | 76754683 | ||||||
| chr17:76754683 | C | CAAA | 13 | a0001c0001t0001g0130 a0001c0001t0001g0157 a0001c0001t0002g0127 others(10): Show |
13 | HG00609.hp2 HG01069.hp1 HG01258.hp1 others(10): Show |
intron_variant | MODIFIER | c.682+610_682+612dup others(3): Show |
MFSD11 | ENSG00000092931.12 | transcript | ENST00000685175.1 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr17 | 76754683 | ||||||
| chr17:76754761 | A | G | 1 | a0001c0001t0003g0014 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.682+674A>G | MFSD11 | ENSG00000092931.12 | transcript | ENST00000685175.1 | protein_coding | 8/12 | chr17 | 76754761 | |||||||
| chr17:76754807 | C | G | 1 | a0001c0001t0002g0082 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.682+720C>G | MFSD11 | ENSG00000092931.12 | transcript | ENST00000685175.1 | protein_coding | 8/12 | chr17 | 76754807 | |||||||
| chr17:76755038 | C | T | 7 | a0001c0001t0001g0046 a0001c0001t0001g0064 a0001c0001t0001g0068 others(4): Show |
7 | HG02258.hp1 HG02486.hp2 HG02723.hp1 others(4): Show |
intron_variant | MODIFIER | c.682+951C>T | MFSD11 | ENSG00000092931.12 | transcript | ENST00000685175.1 | protein_coding | 8/12 | chr17 | 76755038 | |||||||
| chr17:76755212 | C | CA | 13 | a0001c0001t0001g0010 a0001c0001t0001g0099 a0001c0001t0001g0177 others(10): Show |
14 | HG02056.hp1 HG02056.hp2 HG02293.hp1 others(11): Show |
intron_variant | MODIFIER | c.682+1140dupA | MFSD11 | ENSG00000092931.12 | transcript | ENST00000685175.1 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr17 | 76755212 | ||||||
| chr17:76755239 | A | G | 2 | a0001c0001t0001g0178 a0001c0001t0001g0237 |
2 | HG01074.hp1 HG01258.hp2 |
intron_variant | MODIFIER | c.682+1152A>G | MFSD11 | ENSG00000092931.12 | transcript | ENST00000685175.1 | protein_coding | 8/12 | chr17 | 76755239 | |||||||
| chr17:76755246 | A | G | 2 | a0001c0006t0007g0042 a0001c0006t0007g0043 |
2 | HG02602.hp1 HG02735.hp1 |
intron_variant | MODIFIER | c.682+1159A>G | MFSD11 | ENSG00000092931.12 | transcript | ENST00000685175.1 | protein_coding | 8/12 | chr17 | 76755246 | |||||||
| chr17:76755344 | T | A | 1 | a0001c0001t0001g0147 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.682+1257T>A | MFSD11 | ENSG00000092931.12 | transcript | ENST00000685175.1 | protein_coding | 8/12 | chr17 | 76755344 | |||||||
| chr17:76755387 | G | C | 302 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0010 others(299): Show |
315 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(312): Show |
intron_variant | MODIFIER | c.682+1300G>C | MFSD11 | ENSG00000092931.12 | transcript | ENST00000685175.1 | protein_coding | 8/12 | chr17 | 76755387 | |||||||
| chr17:76755429 | A | G | 7 | a0001c0001t0005g0035 a0001c0001t0005g0036 a0001c0001t0005g0037 others(4): Show |
7 | HG02602.hp1 HG02630.hp1 HG02735.hp1 others(4): Show |
intron_variant | MODIFIER | c.682+1342A>G | MFSD11 | ENSG00000092931.12 | transcript | ENST00000685175.1 | protein_coding | 8/12 | chr17 | 76755429 | |||||||
| chr17:76755574 | C | A | 1 | a0001c0001t0001g0069 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.682+1487C>A | MFSD11 | ENSG00000092931.12 | transcript | ENST00000685175.1 | protein_coding | 8/12 | chr17 | 76755574 | |||||||
| chr17:76755697 | T | C | 2 | a0001c0006t0007g0042 a0001c0006t0007g0043 |
2 | HG02602.hp1 HG02735.hp1 |
intron_variant | MODIFIER | c.682+1610T>C | MFSD11 | ENSG00000092931.12 | transcript | ENST00000685175.1 | protein_coding | 8/12 | chr17 | 76755697 | |||||||
| chr17:76755708 | A | G | 2 | a0001c0006t0007g0042 a0001c0006t0007g0043 |
2 | HG02602.hp1 HG02735.hp1 |
intron_variant | MODIFIER | c.682+1621A>G | MFSD11 | ENSG00000092931.12 | transcript | ENST00000685175.1 | protein_coding | 8/12 | chr17 | 76755708 | |||||||
| chr17:76755724 | GTATATGT others(3): Show |
G | 4 | a0001c0001t0001g0048 a0001c0001t0001g0058 a0001c0001t0001g0171 others(1): Show |
4 | HG00544.hp1 HG00741.hp1 HG02683.hp1 others(1): Show |
intron_variant | MODIFIER | c.682+1655_682+1664d others(12): Show |
MFSD11 | ENSG00000092931.12 | transcript | ENST00000685175.1 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr17 | 76755724 | ||||||
| chr17:76755734 | ATATATGT others(17): Show |
A | 15 | a0001c0001t0001g0286 a0001c0001t0001g0299 a0001c0001t0001g0300 others(12): Show |
15 | HG01123.hp2 HG02074.hp1 HG03688.hp1 others(12): Show |
intron_variant | MODIFIER | c.682+1653_682+1676d others(26): Show |
MFSD11 | ENSG00000092931.12 | transcript | ENST00000685175.1 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr17 | 76755734 | ||||||
| chr17:76755739 | T | C | 1 | a0001c0001t0001g0331 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.682+1652T>C | MFSD11 | ENSG00000092931.12 | transcript | ENST00000685175.1 | protein_coding | 8/12 | chr17 | 76755739 | |||||||
| chr17:76755742 | A | G | 1 | a0001c0001t0001g0331 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.682+1655A>G | MFSD11 | ENSG00000092931.12 | transcript | ENST00000685175.1 | protein_coding | 8/12 | chr17 | 76755742 | |||||||
| chr17:76755744 | A | G | 1 | a0001c0001t0001g0331 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.682+1657A>G | MFSD11 | ENSG00000092931.12 | transcript | ENST00000685175.1 | protein_coding | 8/12 | chr17 | 76755744 | |||||||
| chr17:76755746 | A | G | 1 | a0001c0001t0001g0331 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.682+1659A>G | MFSD11 | ENSG00000092931.12 | transcript | ENST00000685175.1 | protein_coding | 8/12 | chr17 | 76755746 | |||||||
| chr17:76755748 | A | G | 1 | a0001c0001t0001g0331 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.682+1661A>G | MFSD11 | ENSG00000092931.12 | transcript | ENST00000685175.1 | protein_coding | 8/12 | chr17 | 76755748 | |||||||
| chr17:76755757 | T | C | 1 | a0001c0001t0001g0331 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.682+1670T>C | MFSD11 | ENSG00000092931.12 | transcript | ENST00000685175.1 | protein_coding | 8/12 | chr17 | 76755757 | |||||||
| chr17:76755758 | G | A | 1 | a0001c0001t0001g0331 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.682+1671G>A | MFSD11 | ENSG00000092931.12 | transcript | ENST00000685175.1 | protein_coding | 8/12 | chr17 | 76755758 | |||||||
| chr17:76755766 | G | A | 1 | a0001c0001t0001g0331 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.682+1679G>A | MFSD11 | ENSG00000092931.12 | transcript | ENST00000685175.1 | protein_coding | 8/12 | chr17 | 76755766 | |||||||
| chr17:76755768 | ACGTGTGT others(11): Show |
A | 1 | a0001c0001t0001g0331 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.682+1682_682+1699d others(20): Show |
MFSD11 | ENSG00000092931.12 | transcript | ENST00000685175.1 | protein_coding | 8/12 | chr17 | 76755768 | |||||||
| chr17:76755769 | CGTGT | C | 42 | a0001c0001t0001g0010 a0001c0001t0001g0067 a0001c0001t0001g0097 others(39): Show |
43 | HG00558.hp1 HG00733.hp1 HG01069.hp2 others(40): Show |
intron_variant | MODIFIER | c.682+1697_682+1700d others(6): Show |
MFSD11 | ENSG00000092931.12 | transcript | ENST00000685175.1 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr17 | 76755769 | ||||||
| chr17:76755782 | G | A | 8 | a0001c0001t0001g0129 a0001c0001t0001g0146 a0001c0001t0003g0015 others(5): Show |
8 | HG01069.hp1 HG02258.hp2 HG02630.hp2 others(5): Show |
intron_variant | MODIFIER | c.682+1695G>A | MFSD11 | ENSG00000092931.12 | transcript | ENST00000685175.1 | protein_coding | 8/12 | chr17 | 76755782 | |||||||
| chr17:76755782 | G | GTATACAT others(1): Show |
17 | a0001c0001t0001g0044 a0001c0001t0001g0046 a0001c0001t0001g0056 others(14): Show |
17 | HG00140.hp1 HG00735.hp2 HG01074.hp2 others(14): Show |
intron_variant | MODIFIER | c.682+1696_682+1697i others(10): Show |
MFSD11 | ENSG00000092931.12 | transcript | ENST00000685175.1 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr17 | 76755782 | ||||||
| chr17:76755782 | G | GTATACAT others(3): Show |
22 | a0001c0001t0001g0007 a0001c0001t0001g0047 a0001c0001t0001g0128 others(19): Show |
22 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(19): Show |
intron_variant | MODIFIER | c.682+1696_682+1697i others(12): Show |
MFSD11 | ENSG00000092931.12 | transcript | ENST00000685175.1 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr17 | 76755782 | ||||||
| chr17:76755782 | G | GTATACAT others(5): Show |
16 | a0001c0001t0001g0007 a0001c0001t0001g0105 a0001c0001t0001g0149 others(13): Show |
16 | HG00280.hp1 HG00323.hp1 HG01928.hp2 others(13): Show |
intron_variant | MODIFIER | c.682+1696_682+1697i others(14): Show |
MFSD11 | ENSG00000092931.12 | transcript | ENST00000685175.1 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr17 | 76755782 | ||||||
| chr17:76755782 | G | GTATACAT others(7): Show |
13 | a0001c0001t0001g0145 a0001c0001t0001g0170 a0001c0001t0001g0232 others(10): Show |
13 | HG00673.hp1 HG01070.hp2 HG01071.hp1 others(10): Show |
intron_variant | MODIFIER | c.682+1696_682+1697i others(16): Show |
MFSD11 | ENSG00000092931.12 | transcript | ENST00000685175.1 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr17 | 76755782 | ||||||
| chr17:76755782 | G | GTATACAT others(9): Show |
5 | a0001c0001t0002g0113 a0001c0001t0002g0126 a0001c0001t0002g0192 others(2): Show |
5 | HG00609.hp1 HG01975.hp1 HG02273.hp1 others(2): Show |
intron_variant | MODIFIER | c.682+1696_682+1697i others(18): Show |
MFSD11 | ENSG00000092931.12 | transcript | ENST00000685175.1 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr17 | 76755782 | ||||||
| chr17:76755782 | G | GTATACAT others(11): Show |
2 | a0001c0001t0002g0229 a0001c0001t0002g0241 |
2 | HG03492.hp1 NA19060.hp2 |
intron_variant | MODIFIER | c.682+1696_682+1697i others(20): Show |
MFSD11 | ENSG00000092931.12 | transcript | ENST00000685175.1 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr17 | 76755782 | ||||||
| chr17:76755782 | G | GTATACAT others(13): Show |
2 | a0001c0001t0001g0101 a0001c0001t0002g0096 |
2 | NA18994.hp1 NA18994.hp2 |
intron_variant | MODIFIER | c.682+1696_682+1697i others(22): Show |
MFSD11 | ENSG00000092931.12 | transcript | ENST00000685175.1 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr17 | 76755782 | ||||||
| chr17:76755782 | GTGTGTAT others(13): Show |
G | 1 | a0001c0001t0002g0313 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.682+1697_682+1716d others(22): Show |
MFSD11 | ENSG00000092931.12 | transcript | ENST00000685175.1 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr17 | 76755782 | ||||||
| chr17:76755784 | G | A | 260 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0044 others(257): Show |
271 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(268): Show |
intron_variant | MODIFIER | c.682+1697G>A | MFSD11 | ENSG00000092931.12 | transcript | ENST00000685175.1 | protein_coding | 8/12 | chr17 | 76755784 | |||||||
| chr17:76755785 | T | C | 7 | a0001c0001t0001g0146 a0001c0001t0003g0015 a0001c0001t0004g0030 others(4): Show |
7 | HG01069.hp1 HG02258.hp2 HG02630.hp2 others(4): Show |
intron_variant | MODIFIER | c.682+1698T>C | MFSD11 | ENSG00000092931.12 | transcript | ENST00000685175.1 | protein_coding | 8/12 | chr17 | 76755785 | |||||||
| chr17:76755785 | T | TAC | 3 | a0001c0001t0001g0103 a0001c0001t0001g0164 a0001c0001t0008g0104 |
3 | HG00639.hp2 HG01243.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.682+1698_682+1699i others(4): Show |
MFSD11 | ENSG00000092931.12 | transcript | ENST00000685175.1 | protein_coding | 8/12 | chr17 | 76755785 | |||||||
| chr17:76755786 | G | A | 260 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0044 others(257): Show |
271 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(268): Show |
intron_variant | MODIFIER | c.682+1699G>A | MFSD11 | ENSG00000092931.12 | transcript | ENST00000685175.1 | protein_coding | 8/12 | chr17 | 76755786 | |||||||
| chr17:76755787 | T | C | 170 | a0001c0001t0001g0003 a0001c0001t0001g0048 a0001c0001t0001g0050 others(167): Show |
179 | HG00140.hp2 HG00280.hp2 HG00423.hp1 others(176): Show |
intron_variant | MODIFIER | c.682+1700T>C | MFSD11 | ENSG00000092931.12 | transcript | ENST00000685175.1 | protein_coding | 8/12 | chr17 | 76755787 | |||||||
| chr17:76755791 | C | CATATATA others(7): Show |
2 | a0001c0001t0005g0037 a0001c0001t0005g0039 |
2 | HG02630.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.682+1713_682+1726d others(16): Show |
MFSD11 | ENSG00000092931.12 | transcript | ENST00000685175.1 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr17 | 76755791 | ||||||
| chr17:76755791 | C | T | 258 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0044 others(255): Show |
269 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(266): Show |
intron_variant | MODIFIER | c.682+1704C>T | MFSD11 | ENSG00000092931.12 | transcript | ENST00000685175.1 | protein_coding | 8/12 | chr17 | 76755791 | |||||||
| chr17:76755807 | T | C | 1 | a0001c0001t0002g0313 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.682+1720T>C | MFSD11 | ENSG00000092931.12 | transcript | ENST00000685175.1 | protein_coding | 8/12 | chr17 | 76755807 | |||||||
| chr17:76755808 | ATATATTT others(4): Show |
A | 1 | a0001c0001t0004g0012 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.682+1723_682+1733d others(13): Show |
MFSD11 | ENSG00000092931.12 | transcript | ENST00000685175.1 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr17 | 76755808 | ||||||
| chr17:76755812 | A | ATATATAT others(4): Show |
5 | a0001c0001t0001g0141 a0001c0001t0001g0225 a0001c0001t0001g0296 others(2): Show |
5 | HG02486.hp1 NA18945.hp1 NA18977.hp2 others(2): Show |
intron_variant | MODIFIER | c.682+1726_682+1727i others(13): Show |
MFSD11 | ENSG00000092931.12 | transcript | ENST00000685175.1 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr17 | 76755812 | ||||||
| chr17:76755812 | A | ATATATAT others(6): Show |
3 | a0001c0001t0002g0089 a0001c0001t0002g0110 a0001c0001t0006g0325 |
3 | HG01081.hp1 HG01884.hp2 NA19007.hp1 |
intron_variant | MODIFIER | c.682+1726_682+1727i others(15): Show |
MFSD11 | ENSG00000092931.12 | transcript | ENST00000685175.1 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr17 | 76755812 | ||||||
| chr17:76755812 | A | ATATATAT others(8): Show |
5 | a0001c0001t0001g0249 a0001c0001t0002g0002 a0001c0001t0002g0246 others(2): Show |
5 | HG00642.hp2 HG01099.hp1 HG02165.hp1 others(2): Show |
intron_variant | MODIFIER | c.682+1726_682+1727i others(17): Show |
MFSD11 | ENSG00000092931.12 | transcript | ENST00000685175.1 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr17 | 76755812 | ||||||
| chr17:76755812 | A | ATATATAT others(10): Show |
1 | a0001c0001t0002g0083 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.682+1726_682+1727i others(19): Show |
MFSD11 | ENSG00000092931.12 | transcript | ENST00000685175.1 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr17 | 76755812 | ||||||
| chr17:76755812 | A | ATATATAT others(20): Show |
1 | a0001c0002t0001g0004 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.682+1726_682+1727i others(29): Show |
MFSD11 | ENSG00000092931.12 | transcript | ENST00000685175.1 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr17 | 76755812 | ||||||
| chr17:76755812 | A | ATATATAT others(22): Show |
1 | a0001c0002t0001g0004 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.682+1726_682+1727i others(31): Show |
MFSD11 | ENSG00000092931.12 | transcript | ENST00000685175.1 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr17 | 76755812 | ||||||
| chr17:76755812 | A | ATATATAT others(16): Show |
1 | a0001c0001t0002g0005 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.682+1726_682+1727i others(25): Show |
MFSD11 | ENSG00000092931.12 | transcript | ENST00000685175.1 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr17 | 76755812 | ||||||
| chr17:76755812 | A | ATATATAT others(17): Show |
1 | a0001c0002t0001g0074 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.682+1726_682+1727i others(26): Show |
MFSD11 | ENSG00000092931.12 | transcript | ENST00000685175.1 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr17 | 76755812 | ||||||
| chr17:76755812 | A | ATATATAT others(10): Show |
3 | a0001c0001t0001g0213 a0001c0001t0002g0084 a0001c0001t0002g0118 |
3 | HG00544.hp2 HG03927.hp2 HG04184.hp1 |
intron_variant | MODIFIER | c.682+1726_682+1727i others(19): Show |
MFSD11 | ENSG00000092931.12 | transcript | ENST00000685175.1 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr17 | 76755812 | ||||||
| chr17:76755812 | A | ATATATAT others(11): Show |
1 | a0001c0001t0002g0082 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.682+1726_682+1727i others(20): Show |
MFSD11 | ENSG00000092931.12 | transcript | ENST00000685175.1 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr17 | 76755812 | ||||||
| chr17:76755812 | A | ATATATAT others(13): Show |
1 | a0001c0001t0002g0114 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.682+1726_682+1727i others(22): Show |
MFSD11 | ENSG00000092931.12 | transcript | ENST00000685175.1 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr17 | 76755812 | ||||||
| chr17:76755812 | A | ATATATAT others(16): Show |
1 | a0001c0002t0001g0075 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.682+1726_682+1727i others(25): Show |
MFSD11 | ENSG00000092931.12 | transcript | ENST00000685175.1 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr17 | 76755812 | ||||||
| chr17:76755812 | A | ATATATAT others(8): Show |
3 | a0001c0001t0002g0123 a0001c0001t0002g0182 a0001c0001t0002g0208 |
3 | HG02083.hp1 NA18952.hp2 NA18983.hp1 |
intron_variant | MODIFIER | c.682+1726_682+1727i others(17): Show |
MFSD11 | ENSG00000092931.12 | transcript | ENST00000685175.1 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr17 | 76755812 | ||||||
| chr17:76755812 | A | ATATATAT others(9): Show |
3 | a0001c0001t0001g0237 a0001c0001t0002g0106 a0001c0004t0001g0131 |
3 | HG01074.hp1 HG02071.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.682+1726_682+1727i others(18): Show |
MFSD11 | ENSG00000092931.12 | transcript | ENST00000685175.1 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr17 | 76755812 | ||||||
| chr17:76755812 | A | ATATATAT others(10): Show |
1 | a0001c0001t0002g0005 | 1 | NA19055.hp2 | intron_variant | MODIFIER | c.682+1726_682+1727i others(19): Show |
MFSD11 | ENSG00000092931.12 | transcript | ENST00000685175.1 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr17 | 76755812 | ||||||
| chr17:76755812 | A | ATATATAT others(12): Show |
1 | a0001c0001t0001g0133 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.682+1726_682+1727i others(21): Show |
MFSD11 | ENSG00000092931.12 | transcript | ENST00000685175.1 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr17 | 76755812 | ||||||
| chr17:76755812 | A | ATATATAT others(6): Show |
9 | a0001c0001t0001g0148 a0001c0001t0002g0006 a0001c0001t0002g0085 others(6): Show |
9 | HG00597.hp2 HG00621.hp1 HG02004.hp1 others(6): Show |
intron_variant | MODIFIER | c.682+1726_682+1727i others(15): Show |
MFSD11 | ENSG00000092931.12 | transcript | ENST00000685175.1 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr17 | 76755812 | ||||||
| chr17:76755812 | A | ATATATAT others(7): Show |
6 | a0001c0001t0001g0158 a0001c0001t0001g0178 a0001c0001t0001g0324 others(3): Show |
6 | HG01258.hp2 HG03017.hp1 HG03540.hp1 others(3): Show |
intron_variant | MODIFIER | c.682+1726_682+1727i others(16): Show |
MFSD11 | ENSG00000092931.12 | transcript | ENST00000685175.1 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr17 | 76755812 | ||||||
| chr17:76755812 | A | ATATATAT others(8): Show |
5 | a0001c0001t0001g0087 a0001c0001t0002g0002 a0001c0001t0002g0109 others(2): Show |
5 | HG01069.hp1 HG02148.hp1 HG02258.hp2 others(2): Show |
intron_variant | MODIFIER | c.682+1726_682+1727i others(17): Show |
MFSD11 | ENSG00000092931.12 | transcript | ENST00000685175.1 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr17 | 76755812 | ||||||
| chr17:76755812 | A | ATATATAT others(12): Show |
1 | a0001c0001t0002g0111 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.682+1726_682+1727i others(21): Show |
MFSD11 | ENSG00000092931.12 | transcript | ENST00000685175.1 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr17 | 76755812 | ||||||
| chr17:76755812 | A | ATATATAT others(4): Show |
9 | a0001c0001t0001g0068 a0001c0001t0001g0179 a0001c0001t0001g0318 others(6): Show |
9 | HG00735.hp1 HG02602.hp1 HG02698.hp1 others(6): Show |
intron_variant | MODIFIER | c.682+1726_682+1727i others(13): Show |
MFSD11 | ENSG00000092931.12 | transcript | ENST00000685175.1 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr17 | 76755812 | ||||||
| chr17:76755812 | A | ATATATAT others(5): Show |
5 | a0001c0001t0001g0116 a0001c0001t0001g0147 a0001c0001t0002g0001 others(2): Show |
5 | HG01361.hp2 HG01891.hp2 HG02698.hp2 others(2): Show |
intron_variant | MODIFIER | c.682+1726_682+1727i others(14): Show |
MFSD11 | ENSG00000092931.12 | transcript | ENST00000685175.1 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr17 | 76755812 | ||||||
| chr17:76755812 | A | ATATATAT others(6): Show |
8 | a0001c0001t0001g0093 a0001c0001t0001g0139 a0001c0001t0001g0270 others(5): Show |
8 | HG01109.hp2 HG02055.hp2 HG02683.hp1 others(5): Show |
intron_variant | MODIFIER | c.682+1726_682+1727i others(15): Show |
MFSD11 | ENSG00000092931.12 | transcript | ENST00000685175.1 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr17 | 76755812 | ||||||
| chr17:76755812 | A | ATATATAT others(7): Show |
2 | a0001c0001t0002g0081 a0001c0001t0002g0108 |
2 | HG02080.hp1 NA19066.hp1 |
intron_variant | MODIFIER | c.682+1726_682+1727i others(16): Show |
MFSD11 | ENSG00000092931.12 | transcript | ENST00000685175.1 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr17 | 76755812 | ||||||
| chr17:76755812 | A | ATATATAT others(8): Show |
3 | a0001c0001t0001g0171 a0001c0001t0004g0030 a0001c0001t0004g0034 |
3 | HG00741.hp1 HG02886.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.682+1726_682+1727i others(17): Show |
MFSD11 | ENSG00000092931.12 | transcript | ENST00000685175.1 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr17 | 76755812 | ||||||
| chr17:76755812 | A | ATATATAT others(9): Show |
1 | a0001c0001t0002g0314 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.682+1726_682+1727i others(18): Show |
MFSD11 | ENSG00000092931.12 | transcript | ENST00000685175.1 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr17 | 76755812 | ||||||
| chr17:76755812 | A | ATATATAT others(3): Show |
9 | a0001c0001t0001g0130 a0001c0001t0002g0076 a0001c0001t0002g0159 others(6): Show |
9 | HG02040.hp2 HG02056.hp2 HG02145.hp2 others(6): Show |
intron_variant | MODIFIER | c.682+1726_682+1727i others(12): Show |
MFSD11 | ENSG00000092931.12 | transcript | ENST00000685175.1 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr17 | 76755812 | ||||||
| chr17:76755812 | A | ATATATAT others(4): Show |
9 | a0001c0001t0001g0146 a0001c0001t0001g0160 a0001c0001t0001g0162 others(6): Show |
9 | HG02300.hp1 HG04115.hp1 NA18952.hp1 others(6): Show |
intron_variant | MODIFIER | c.682+1726_682+1727i others(13): Show |
MFSD11 | ENSG00000092931.12 | transcript | ENST00000685175.1 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr17 | 76755812 | ||||||
| chr17:76755812 | A | ATATATAT others(5): Show |
1 | a0001c0001t0002g0214 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.682+1726_682+1727i others(14): Show |
MFSD11 | ENSG00000092931.12 | transcript | ENST00000685175.1 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr17 | 76755812 | ||||||
| chr17:76755812 | A | ATATATAT others(8): Show |
1 | a0001c0001t0004g0032 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.682+1726_682+1727i others(17): Show |
MFSD11 | ENSG00000092931.12 | transcript | ENST00000685175.1 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr17 | 76755812 | ||||||
| chr17:76755812 | A | ATATATTT others(3): Show |
7 | a0001c0001t0001g0134 a0001c0001t0001g0138 a0001c0001t0001g0174 others(4): Show |
7 | HG00280.hp2 HG00423.hp1 HG00642.hp1 others(4): Show |
intron_variant | MODIFIER | c.682+1726_682+1727i others(12): Show |
MFSD11 | ENSG00000092931.12 | transcript | ENST00000685175.1 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr17 | 76755812 | ||||||
| chr17:76755812 | A | ATATATTT others(4): Show |
2 | a0001c0001t0001g0140 a0001c0001t0001g0260 |
2 | HG02273.hp2 NA19000.hp1 |
intron_variant | MODIFIER | c.682+1726_682+1727i others(13): Show |
MFSD11 | ENSG00000092931.12 | transcript | ENST00000685175.1 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr17 | 76755812 | ||||||
| chr17:76755812 | A | ATATATTT others(6): Show |
1 | a0001c0001t0002g0091 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.682+1726_682+1727i others(15): Show |
MFSD11 | ENSG00000092931.12 | transcript | ENST00000685175.1 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr17 | 76755812 | ||||||
| chr17:76755812 | A | ATATTTTT others(3): Show |
1 | a0001c0001t0002g0240 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.682+1726_682+1727i others(12): Show |
MFSD11 | ENSG00000092931.12 | transcript | ENST00000685175.1 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr17 | 76755812 | ||||||
| chr17:76755812 | A | ATTTTTTT others(4): Show |
1 | a0001c0001t0001g0161 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.682+1743_682+1753d others(13): Show |
MFSD11 | ENSG00000092931.12 | transcript | ENST00000685175.1 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr17 | 76755812 | ||||||
| chr17:76755812 | A | T | 41 | a0001c0001t0001g0007 a0001c0001t0001g0044 a0001c0001t0001g0046 others(38): Show |
41 | HG00323.hp1 HG00558.hp1 HG00609.hp1 others(38): Show |
intron_variant | MODIFIER | c.682+1725A>T | MFSD11 | ENSG00000092931.12 | transcript | ENST00000685175.1 | protein_coding | 8/12 | chr17 | 76755812 | |||||||
| chr17:76755812 | ATTT | A | 8 | a0001c0001t0001g0010 a0001c0001t0001g0099 a0001c0001t0001g0284 others(5): Show |
9 | HG02809.hp2 HG02818.hp2 HG02895.hp1 others(6): Show |
intron_variant | MODIFIER | c.682+1751_682+1753d others(5): Show |
MFSD11 | ENSG00000092931.12 | transcript | ENST00000685175.1 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr17 | 76755812 | ||||||
| chr17:76755812 | ATTTTT | A | 25 | a0001c0001t0001g0097 a0001c0001t0001g0098 a0001c0001t0001g0272 others(22): Show |
25 | HG01069.hp2 HG01071.hp2 HG01123.hp2 others(22): Show |
intron_variant | MODIFIER | c.682+1749_682+1753d others(7): Show |
MFSD11 | ENSG00000092931.12 | transcript | ENST00000685175.1 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr17 | 76755812 | ||||||
| chr17:76755813 | T | TA | 3 | a0001c0001t0003g0024 a0001c0001t0003g0040 a0001c0001t0003g0041 |
3 | HG01891.hp1 HG02647.hp2 HG02717.hp1 |
intron_variant | MODIFIER | c.682+1726_682+1727i others(3): Show |
MFSD11 | ENSG00000092931.12 | transcript | ENST00000685175.1 | protein_coding | 8/12 | chr17 | 76755813 | |||||||
| chr17:76755813 | T | TATATATA | 3 | a0001c0001t0001g0150 a0001c0001t0001g0252 a0001c0001t0001g0257 |
3 | HG00733.hp2 NA18993.hp2 NA19001.hp2 |
intron_variant | MODIFIER | c.682+1726_682+1727i others(9): Show |
MFSD11 | ENSG00000092931.12 | transcript | ENST00000685175.1 | protein_coding | 8/12 | chr17 | 76755813 | |||||||
| chr17:76755813 | T | TATATATA others(2): Show |
6 | a0001c0001t0001g0051 a0001c0001t0001g0052 a0001c0001t0001g0053 others(3): Show |
6 | HG01123.hp1 HG03490.hp1 HG03579.hp2 others(3): Show |
intron_variant | MODIFIER | c.682+1726_682+1727i others(11): Show |
MFSD11 | ENSG00000092931.12 | transcript | ENST00000685175.1 | protein_coding | 8/12 | chr17 | 76755813 | |||||||
| chr17:76755813 | T | TATATATA others(4): Show |
5 | a0001c0001t0001g0065 a0001c0001t0001g0142 a0001c0001t0002g0071 others(2): Show |
5 | HG01928.hp1 HG02074.hp2 HG02148.hp2 others(2): Show |
intron_variant | MODIFIER | c.682+1726_682+1727i others(13): Show |
MFSD11 | ENSG00000092931.12 | transcript | ENST00000685175.1 | protein_coding | 8/12 | chr17 | 76755813 | |||||||
| chr17:76755813 | T | TATATATA others(6): Show |
10 | a0001c0001t0001g0058 a0001c0001t0001g0200 a0001c0001t0001g0224 others(7): Show |
10 | HG00423.hp2 HG00597.hp1 HG02004.hp2 others(7): Show |
intron_variant | MODIFIER | c.682+1726_682+1727i others(15): Show |
MFSD11 | ENSG00000092931.12 | transcript | ENST00000685175.1 | protein_coding | 8/12 | chr17 | 76755813 | |||||||
| chr17:76755813 | T | TATATATA others(8): Show |
6 | a0001c0001t0001g0048 a0001c0001t0001g0242 a0001c0001t0001g0243 others(3): Show |
6 | HG00544.hp1 HG00558.hp2 NA18960.hp2 others(3): Show |
intron_variant | MODIFIER | c.682+1726_682+1727i others(17): Show |
MFSD11 | ENSG00000092931.12 | transcript | ENST00000685175.1 | protein_coding | 8/12 | chr17 | 76755813 | |||||||
| chr17:76755813 | T | TATATATA others(10): Show |
7 | a0001c0001t0001g0117 a0001c0001t0002g0197 a0001c0001t0002g0199 others(4): Show |
7 | HG02040.hp1 HG03490.hp2 NA18941.hp2 others(4): Show |
intron_variant | MODIFIER | c.682+1726_682+1727i others(19): Show |
MFSD11 | ENSG00000092931.12 | transcript | ENST00000685175.1 | protein_coding | 8/12 | chr17 | 76755813 | |||||||
| chr17:76755813 | T | TATATATA others(12): Show |
4 | a0001c0001t0001g0196 a0001c0001t0001g0251 a0001c0001t0002g0183 others(1): Show |
4 | HG01978.hp1 NA18953.hp2 NA18993.hp1 others(1): Show |
intron_variant | MODIFIER | c.682+1726_682+1727i others(21): Show |
MFSD11 | ENSG00000092931.12 | transcript | ENST00000685175.1 | protein_coding | 8/12 | chr17 | 76755813 | |||||||
| chr17:76755813 | T | TATATATA others(22): Show |
1 | a0001c0001t0001g0050 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.682+1726_682+1727i others(31): Show |
MFSD11 | ENSG00000092931.12 | transcript | ENST00000685175.1 | protein_coding | 8/12 | chr17 | 76755813 | |||||||
| chr17:76755814 | T | A | 21 | a0001c0001t0001g0101 a0001c0001t0001g0164 a0001c0001t0001g0176 others(18): Show |
21 | HG00099.hp2 HG01192.hp1 HG01243.hp2 others(18): Show |
intron_variant | MODIFIER | c.682+1727T>A | MFSD11 | ENSG00000092931.12 | transcript | ENST00000685175.1 | protein_coding | 8/12 | chr17 | 76755814 | |||||||
| chr17:76755815 | T | A | 21 | a0001c0001t0001g0117 a0001c0001t0001g0196 a0001c0001t0001g0200 others(18): Show |
21 | HG00423.hp2 HG00597.hp1 HG01891.hp1 others(18): Show |
intron_variant | MODIFIER | c.682+1728T>A | MFSD11 | ENSG00000092931.12 | transcript | ENST00000685175.1 | protein_coding | 8/12 | chr17 | 76755815 | |||||||
| chr17:76755816 | T | A | 14 | a0001c0001t0001g0101 a0001c0001t0001g0164 a0001c0001t0001g0176 others(11): Show |
14 | HG01243.hp2 HG01975.hp2 HG02027.hp2 others(11): Show |
intron_variant | MODIFIER | c.682+1729T>A | MFSD11 | ENSG00000092931.12 | transcript | ENST00000685175.1 | protein_coding | 8/12 | chr17 | 76755816 | |||||||
| chr17:76755817 | T | A | 19 | a0001c0001t0001g0010 a0001c0001t0001g0099 a0001c0001t0001g0117 others(16): Show |
20 | HG00597.hp1 HG02040.hp1 HG02647.hp2 others(17): Show |
intron_variant | MODIFIER | c.682+1730T>A | MFSD11 | ENSG00000092931.12 | transcript | ENST00000685175.1 | protein_coding | 8/12 | chr17 | 76755817 | |||||||
| chr17:76755818 | T | A | 7 | a0001c0001t0001g0101 a0001c0001t0001g0164 a0001c0001t0001g0176 others(4): Show |
7 | HG01243.hp2 HG01975.hp2 HG06807.hp1 others(4): Show |
intron_variant | MODIFIER | c.682+1731T>A | MFSD11 | ENSG00000092931.12 | transcript | ENST00000685175.1 | protein_coding | 8/12 | chr17 | 76755818 | |||||||
| chr17:76755819 | T | A | 37 | a0001c0001t0001g0010 a0001c0001t0001g0097 a0001c0001t0001g0098 others(34): Show |
38 | HG01069.hp2 HG01071.hp2 HG01123.hp2 others(35): Show |
intron_variant | MODIFIER | c.682+1732T>A | MFSD11 | ENSG00000092931.12 | transcript | ENST00000685175.1 | protein_coding | 8/12 | chr17 | 76755819 | |||||||
| chr17:76755820 | T | A | 3 | a0001c0001t0001g0164 a0001c0001t0001g0176 a0001c0001t0001g0300 |
3 | HG01243.hp2 HG06807.hp1 NA18968.hp2 |
intron_variant | MODIFIER | c.682+1733T>A | MFSD11 | ENSG00000092931.12 | transcript | ENST00000685175.1 | protein_coding | 8/12 | chr17 | 76755820 | |||||||
| chr17:76755821 | T | A | 36 | a0001c0001t0001g0010 a0001c0001t0001g0097 a0001c0001t0001g0098 others(33): Show |
37 | HG01069.hp2 HG01071.hp2 HG01123.hp2 others(34): Show |
intron_variant | MODIFIER | c.682+1734T>A | MFSD11 | ENSG00000092931.12 | transcript | ENST00000685175.1 | protein_coding | 8/12 | chr17 | 76755821 | |||||||
| chr17:76755822 | T | A | 2 | a0001c0001t0001g0176 a0001c0001t0001g0300 |
2 | HG06807.hp1 NA18968.hp2 |
intron_variant | MODIFIER | c.682+1735T>A | MFSD11 | ENSG00000092931.12 | transcript | ENST00000685175.1 | protein_coding | 8/12 | chr17 | 76755822 | |||||||
| chr17:76755823 | T | A | 32 | a0001c0001t0001g0010 a0001c0001t0001g0097 a0001c0001t0001g0098 others(29): Show |
33 | HG01069.hp2 HG01071.hp2 HG01123.hp2 others(30): Show |
intron_variant | MODIFIER | c.682+1736T>A | MFSD11 | ENSG00000092931.12 | transcript | ENST00000685175.1 | protein_coding | 8/12 | chr17 | 76755823 | |||||||
| chr17:76755825 | T | A | 13 | a0001c0001t0001g0010 a0001c0001t0001g0097 a0001c0001t0001g0099 others(10): Show |
14 | HG01069.hp2 HG01071.hp2 HG02622.hp2 others(11): Show |
intron_variant | MODIFIER | c.682+1738T>A | MFSD11 | ENSG00000092931.12 | transcript | ENST00000685175.1 | protein_coding | 8/12 | chr17 | 76755825 | |||||||
| chr17:76755845 | T | C | 2 | a0001c0006t0007g0042 a0001c0006t0007g0043 |
2 | HG02602.hp1 HG02735.hp1 |
intron_variant | MODIFIER | c.682+1758T>C | MFSD11 | ENSG00000092931.12 | transcript | ENST00000685175.1 | protein_coding | 8/12 | chr17 | 76755845 | |||||||
| chr17:76755882 | G | A | 2 | a0001c0006t0007g0042 a0001c0006t0007g0043 |
2 | HG02602.hp1 HG02735.hp1 |
intron_variant | MODIFIER | c.682+1795G>A | MFSD11 | ENSG00000092931.12 | transcript | ENST00000685175.1 | protein_coding | 8/12 | chr17 | 76755882 | |||||||
| chr17:76755884 | T | C | 2 | a0001c0006t0007g0042 a0001c0006t0007g0043 |
2 | HG02602.hp1 HG02735.hp1 |
intron_variant | MODIFIER | c.682+1797T>C | MFSD11 | ENSG00000092931.12 | transcript | ENST00000685175.1 | protein_coding | 8/12 | chr17 | 76755884 | |||||||
| chr17:76756012 | T | C | 2 | a0001c0006t0007g0042 a0001c0006t0007g0043 |
2 | HG02602.hp1 HG02735.hp1 |
intron_variant | MODIFIER | c.682+1925T>C | MFSD11 | ENSG00000092931.12 | transcript | ENST00000685175.1 | protein_coding | 8/12 | chr17 | 76756012 | |||||||
| chr17:76756122 | A | AT | 48 | a0001c0001t0001g0055 a0001c0001t0001g0101 a0001c0001t0001g0139 others(45): Show |
48 | HG00735.hp2 HG01069.hp1 HG01891.hp1 others(45): Show |
intron_variant | MODIFIER | c.682+2053dupT | MFSD11 | ENSG00000092931.12 | transcript | ENST00000685175.1 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr17 | 76756122 | ||||||
| chr17:76756304 | A | G | 2 | a0001c0001t0002g0081 a0001c0001t0002g0107 |
2 | HG02080.hp1 HG02132.hp1 |
intron_variant | MODIFIER | c.682+2217A>G | MFSD11 | ENSG00000092931.12 | transcript | ENST00000685175.1 | protein_coding | 8/12 | chr17 | 76756304 | |||||||
| chr17:76756415 | C | T | 1 | a0001c0001t0001g0139 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.682+2328C>T | MFSD11 | ENSG00000092931.12 | transcript | ENST00000685175.1 | protein_coding | 8/12 | chr17 | 76756415 | |||||||
| chr17:76756425 | G | A | 301 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0010 others(298): Show |
314 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(311): Show |
intron_variant | MODIFIER | c.682+2338G>A | MFSD11 | ENSG00000092931.12 | transcript | ENST00000685175.1 | protein_coding | 8/12 | chr17 | 76756425 | |||||||
| chr17:76756466 | T | G | 2 | a0001c0006t0007g0042 a0001c0006t0007g0043 |
2 | HG02602.hp1 HG02735.hp1 |
intron_variant | MODIFIER | c.682+2379T>G | MFSD11 | ENSG00000092931.12 | transcript | ENST00000685175.1 | protein_coding | 8/12 | chr17 | 76756466 | |||||||
| chr17:76756478 | T | A | 5 | a0001c0001t0005g0035 a0001c0001t0005g0036 a0001c0001t0005g0037 others(2): Show |
5 | HG02630.hp1 HG02886.hp2 HG03209.hp1 others(2): Show |
intron_variant | MODIFIER | c.682+2391T>A | MFSD11 | ENSG00000092931.12 | transcript | ENST00000685175.1 | protein_coding | 8/12 | chr17 | 76756478 | |||||||
| chr17:76756560 | G | A | 5 | a0001c0001t0004g0030 a0001c0001t0004g0031 a0001c0001t0004g0032 others(2): Show |
5 | HG01069.hp1 HG02258.hp2 HG02630.hp2 others(2): Show |
intron_variant | MODIFIER | c.682+2473G>A | MFSD11 | ENSG00000092931.12 | transcript | ENST00000685175.1 | protein_coding | 8/12 | chr17 | 76756560 | |||||||
| chr17:76756615 | C | T | 2 | a0001c0001t0003g0017 a0001c0001t0003g0018 |
2 | HG02559.hp2 HG02615.hp1 |
intron_variant | MODIFIER | c.682+2528C>T | MFSD11 | ENSG00000092931.12 | transcript | ENST00000685175.1 | protein_coding | 8/12 | chr17 | 76756615 | |||||||
| chr17:76756736 | T | C | 5 | a0001c0001t0004g0030 a0001c0001t0004g0031 a0001c0001t0004g0032 others(2): Show |
5 | HG01069.hp1 HG02258.hp2 HG02630.hp2 others(2): Show |
intron_variant | MODIFIER | c.682+2649T>C | MFSD11 | ENSG00000092931.12 | transcript | ENST00000685175.1 | protein_coding | 8/12 | chr17 | 76756736 | |||||||
| chr17:76756796 | G | T | 2 | a0001c0006t0007g0042 a0001c0006t0007g0043 |
2 | HG02602.hp1 HG02735.hp1 |
intron_variant | MODIFIER | c.682+2709G>T | MFSD11 | ENSG00000092931.12 | transcript | ENST00000685175.1 | protein_coding | 8/12 | chr17 | 76756796 | |||||||
| chr17:76756817 | G | A | 3 | a0001c0002t0001g0004 a0001c0002t0001g0074 a0001c0002t0001g0075 |
4 | HG01243.hp1 HG01884.hp1 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.682+2730G>A | MFSD11 | ENSG00000092931.12 | transcript | ENST00000685175.1 | protein_coding | 8/12 | chr17 | 76756817 | |||||||
| chr17:76756855 | A | G | 1 | a0001c0001t0001g0277 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.682+2768A>G | MFSD11 | ENSG00000092931.12 | transcript | ENST00000685175.1 | protein_coding | 8/12 | chr17 | 76756855 | |||||||
| chr17:76756861 | G | GA | 25 | a0001c0001t0001g0050 a0001c0001t0001g0056 a0001c0001t0001g0093 others(22): Show |
25 | HG01123.hp2 HG02055.hp2 HG02056.hp1 others(22): Show |
intron_variant | MODIFIER | c.682+2790dupA | MFSD11 | ENSG00000092931.12 | transcript | ENST00000685175.1 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr17 | 76756861 | ||||||
| chr17:76757050 | G | C | 1 | a0001c0001t0002g0084 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.682+2963G>C | MFSD11 | ENSG00000092931.12 | transcript | ENST00000685175.1 | protein_coding | 8/12 | chr17 | 76757050 | |||||||
| chr17:76757053 | C | T | 2 | a0001c0006t0007g0042 a0001c0006t0007g0043 |
2 | HG02602.hp1 HG02735.hp1 |
intron_variant | MODIFIER | c.682+2966C>T | MFSD11 | ENSG00000092931.12 | transcript | ENST00000685175.1 | protein_coding | 8/12 | chr17 | 76757053 | |||||||
| chr17:76757370 | G | C | 1 | a0001c0006t0007g0042 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.682+3283G>C | MFSD11 | ENSG00000092931.12 | transcript | ENST00000685175.1 | protein_coding | 8/12 | chr17 | 76757370 | |||||||
| chr17:76757435 | T | C | 2 | a0001c0006t0007g0042 a0001c0006t0007g0043 |
2 | HG02602.hp1 HG02735.hp1 |
intron_variant | MODIFIER | c.682+3348T>C | MFSD11 | ENSG00000092931.12 | transcript | ENST00000685175.1 | protein_coding | 8/12 | chr17 | 76757435 | |||||||
| chr17:76757571 | C | T | 1 | a0001c0001t0002g0218 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.682+3484C>T | MFSD11 | ENSG00000092931.12 | transcript | ENST00000685175.1 | protein_coding | 8/12 | chr17 | 76757571 | |||||||
| chr17:76757630 | C | T | 5 | a0001c0001t0004g0030 a0001c0001t0004g0031 a0001c0001t0004g0032 others(2): Show |
5 | HG01069.hp1 HG02258.hp2 HG02630.hp2 others(2): Show |
intron_variant | MODIFIER | c.682+3543C>T | MFSD11 | ENSG00000092931.12 | transcript | ENST00000685175.1 | protein_coding | 8/12 | chr17 | 76757630 | |||||||
| chr17:76757684 | T | A | 19 | a0001c0001t0003g0013 a0001c0001t0003g0016 a0001c0001t0003g0017 others(16): Show |
19 | HG01891.hp1 HG02559.hp1 HG02559.hp2 others(16): Show |
intron_variant | MODIFIER | c.682+3597T>A | MFSD11 | ENSG00000092931.12 | transcript | ENST00000685175.1 | protein_coding | 8/12 | chr17 | 76757684 | |||||||
| chr17:76757739 | G | A | 1 | a0001c0001t0002g0076 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.682+3652G>A | MFSD11 | ENSG00000092931.12 | transcript | ENST00000685175.1 | protein_coding | 8/12 | chr17 | 76757739 | |||||||
| chr17:76757763 | T | C | 2 | a0001c0006t0007g0042 a0001c0006t0007g0043 |
2 | HG02602.hp1 HG02735.hp1 |
intron_variant | MODIFIER | c.682+3676T>C | MFSD11 | ENSG00000092931.12 | transcript | ENST00000685175.1 | protein_coding | 8/12 | chr17 | 76757763 | |||||||
| chr17:76757782 | A | G | 329 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0010 others(326): Show |
342 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(339): Show |
intron_variant | MODIFIER | c.682+3695A>G | MFSD11 | ENSG00000092931.12 | transcript | ENST00000685175.1 | protein_coding | 8/12 | chr17 | 76757782 | |||||||
| chr17:76757923 | T | C | 2 | a0001c0006t0007g0042 a0001c0006t0007g0043 |
2 | HG02602.hp1 HG02735.hp1 |
intron_variant | MODIFIER | c.682+3836T>C | MFSD11 | ENSG00000092931.12 | transcript | ENST00000685175.1 | protein_coding | 8/12 | chr17 | 76757923 | |||||||
| chr17:76757945 | G | C | 1 | a0001c0001t0003g0024 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.682+3858G>C | MFSD11 | ENSG00000092931.12 | transcript | ENST00000685175.1 | protein_coding | 8/12 | chr17 | 76757945 | |||||||
| chr17:76758218 | T | C | 1 | a0001c0001t0001g0320 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.682+4131T>C | MFSD11 | ENSG00000092931.12 | transcript | ENST00000685175.1 | protein_coding | 8/12 | chr17 | 76758218 | |||||||
| chr17:76758258 | T | A | 2 | a0001c0006t0007g0042 a0001c0006t0007g0043 |
2 | HG02602.hp1 HG02735.hp1 |
intron_variant | MODIFIER | c.682+4171T>A | MFSD11 | ENSG00000092931.12 | transcript | ENST00000685175.1 | protein_coding | 8/12 | chr17 | 76758258 | |||||||
| chr17:76758316 | A | AT | 270 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0044 others(267): Show |
281 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(278): Show |
intron_variant | MODIFIER | c.682+4230dupT | MFSD11 | ENSG00000092931.12 | transcript | ENST00000685175.1 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr17 | 76758316 | ||||||
| chr17:76758385 | G | C | 249 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0044 others(246): Show |
260 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(257): Show |
intron_variant | MODIFIER | c.682+4298G>C | MFSD11 | ENSG00000092931.12 | transcript | ENST00000685175.1 | protein_coding | 8/12 | chr17 | 76758385 | |||||||
| chr17:76758470 | C | G | 11 | a0001c0001t0001g0010 a0001c0001t0001g0097 a0001c0001t0001g0099 others(8): Show |
12 | HG01069.hp2 HG01071.hp2 HG02647.hp1 others(9): Show |
intron_variant | MODIFIER | c.682+4383C>G | MFSD11 | ENSG00000092931.12 | transcript | ENST00000685175.1 | protein_coding | 8/12 | chr17 | 76758470 | |||||||
| chr17:76758556 | A | G | 244 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0044 others(241): Show |
254 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(251): Show |
intron_variant | MODIFIER | c.682+4469A>G | MFSD11 | ENSG00000092931.12 | transcript | ENST00000685175.1 | protein_coding | 8/12 | chr17 | 76758556 | |||||||
| chr17:76758576 | G | C | 32 | a0001c0001t0001g0323 a0001c0001t0002g0005 a0001c0001t0002g0059 others(29): Show |
33 | HG00140.hp2 HG00558.hp1 HG00609.hp1 others(30): Show |
intron_variant | MODIFIER | c.682+4489G>C | MFSD11 | ENSG00000092931.12 | transcript | ENST00000685175.1 | protein_coding | 8/12 | chr17 | 76758576 | |||||||
| chr17:76758581 | C | CA | 69 | a0001c0001t0001g0003 a0001c0001t0001g0044 a0001c0001t0001g0047 others(66): Show |
70 | HG00544.hp1 HG00639.hp1 HG01070.hp1 others(67): Show |
intron_variant | MODIFIER | c.682+4515dupA | MFSD11 | ENSG00000092931.12 | transcript | ENST00000685175.1 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr17 | 76758581 | ||||||
| chr17:76758581 | C | CAA | 30 | a0001c0001t0001g0066 a0001c0001t0001g0097 a0001c0001t0001g0098 others(27): Show |
31 | HG00639.hp2 HG00735.hp2 HG01069.hp1 others(28): Show |
intron_variant | MODIFIER | c.682+4514_682+4515d others(4): Show |
MFSD11 | ENSG00000092931.12 | transcript | ENST00000685175.1 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr17 | 76758581 | ||||||
| chr17:76758581 | CA | C | 10 | a0001c0001t0001g0053 a0001c0001t0001g0099 a0001c0001t0001g0141 others(7): Show |
10 | HG00099.hp1 HG00280.hp1 HG01517.hp1 others(7): Show |
intron_variant | MODIFIER | c.682+4515delA | MFSD11 | ENSG00000092931.12 | transcript | ENST00000685175.1 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr17 | 76758581 | ||||||
| chr17:76758736 | C | T | 285 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0010 others(282): Show |
297 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(294): Show |
intron_variant | MODIFIER | c.682+4649C>T | MFSD11 | ENSG00000092931.12 | transcript | ENST00000685175.1 | protein_coding | 8/12 | chr17 | 76758736 | |||||||
| chr17:76758749 | G | T | 2 | a0001c0006t0007g0042 a0001c0006t0007g0043 |
2 | HG02602.hp1 HG02735.hp1 |
intron_variant | MODIFIER | c.682+4662G>T | MFSD11 | ENSG00000092931.12 | transcript | ENST00000685175.1 | protein_coding | 8/12 | chr17 | 76758749 | |||||||
| chr17:76758973 | A | C | 2 | a0001c0001t0001g0279 a0002c0007t0001g0280 |
2 | HG02257.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.682+4886A>C | MFSD11 | ENSG00000092931.12 | transcript | ENST00000685175.1 | protein_coding | 8/12 | chr17 | 76758973 | |||||||
| chr17:76758993 | C | T | 4 | a0001c0001t0001g0324 a0001c0001t0003g0017 a0001c0001t0003g0018 others(1): Show |
4 | HG01891.hp1 HG02559.hp2 HG02615.hp1 others(1): Show |
intron_variant | MODIFIER | c.682+4906C>T | MFSD11 | ENSG00000092931.12 | transcript | ENST00000685175.1 | protein_coding | 8/12 | chr17 | 76758993 | |||||||
| chr17:76759090 | A | C | 4 | a0001c0001t0001g0324 a0001c0001t0003g0017 a0001c0001t0003g0018 others(1): Show |
4 | HG01891.hp1 HG02559.hp2 HG02615.hp1 others(1): Show |
intron_variant | MODIFIER | c.682+5003A>C | MFSD11 | ENSG00000092931.12 | transcript | ENST00000685175.1 | protein_coding | 8/12 | chr17 | 76759090 | |||||||
| chr17:76759099 | A | C | 50 | a0001c0001t0001g0323 a0001c0001t0002g0002 a0001c0001t0002g0005 others(47): Show |
54 | HG00140.hp2 HG00558.hp1 HG00597.hp2 others(51): Show |
intron_variant | MODIFIER | c.682+5012A>C | MFSD11 | ENSG00000092931.12 | transcript | ENST00000685175.1 | protein_coding | 8/12 | chr17 | 76759099 | |||||||
| chr17:76759110 | A | T | 295 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0010 others(292): Show |
307 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(304): Show |
intron_variant | MODIFIER | c.682+5023A>T | MFSD11 | ENSG00000092931.12 | transcript | ENST00000685175.1 | protein_coding | 8/12 | chr17 | 76759110 | |||||||
| chr17:76759203 | A | G | 1 | a0001c0001t0001g0093 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.682+5116A>G | MFSD11 | ENSG00000092931.12 | transcript | ENST00000685175.1 | protein_coding | 8/12 | chr17 | 76759203 | |||||||
| chr17:76759251 | C | T | 2 | a0001c0001t0002g0082 a0001c0001t0002g0118 |
2 | HG04115.hp2 HG04184.hp1 |
intron_variant | MODIFIER | c.682+5164C>T | MFSD11 | ENSG00000092931.12 | transcript | ENST00000685175.1 | protein_coding | 8/12 | chr17 | 76759251 | |||||||
| chr17:76759266 | T | C | 3 | a0001c0001t0003g0017 a0001c0001t0003g0018 a0001c0001t0003g0040 |
3 | HG01891.hp1 HG02559.hp2 HG02615.hp1 |
intron_variant | MODIFIER | c.682+5179T>C | MFSD11 | ENSG00000092931.12 | transcript | ENST00000685175.1 | protein_coding | 8/12 | chr17 | 76759266 | |||||||
| chr17:76759268 | C | A | 2 | a0001c0006t0007g0042 a0001c0006t0007g0043 |
2 | HG02602.hp1 HG02735.hp1 |
intron_variant | MODIFIER | c.682+5181C>A | MFSD11 | ENSG00000092931.12 | transcript | ENST00000685175.1 | protein_coding | 8/12 | chr17 | 76759268 | |||||||
| chr17:76759289 | C | CT | 6 | a0001c0001t0001g0010 a0001c0001t0001g0099 a0001c0001t0001g0272 others(3): Show |
7 | HG02602.hp1 HG02717.hp2 HG02735.hp1 others(4): Show |
intron_variant | MODIFIER | c.682+5213dupT | MFSD11 | ENSG00000092931.12 | transcript | ENST00000685175.1 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr17 | 76759289 | ||||||
| chr17:76759443 | T | C | 2 | a0001c0006t0007g0042 a0001c0006t0007g0043 |
2 | HG02602.hp1 HG02735.hp1 |
intron_variant | MODIFIER | c.682+5356T>C | MFSD11 | ENSG00000092931.12 | transcript | ENST00000685175.1 | protein_coding | 8/12 | chr17 | 76759443 | |||||||
| chr17:76759444 | A | G | 5 | a0001c0001t0005g0035 a0001c0001t0005g0036 a0001c0001t0005g0037 others(2): Show |
5 | HG02630.hp1 HG02886.hp2 HG03209.hp1 others(2): Show |
intron_variant | MODIFIER | c.682+5357A>G | MFSD11 | ENSG00000092931.12 | transcript | ENST00000685175.1 | protein_coding | 8/12 | chr17 | 76759444 | |||||||
| chr17:76759517 | C | T | 1 | a0001c0001t0001g0329 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.682+5430C>T | MFSD11 | ENSG00000092931.12 | transcript | ENST00000685175.1 | protein_coding | 8/12 | chr17 | 76759517 | |||||||
| chr17:76759634 | T | A | 2 | a0001c0006t0007g0042 a0001c0006t0007g0043 |
2 | HG02602.hp1 HG02735.hp1 |
intron_variant | MODIFIER | c.682+5547T>A | MFSD11 | ENSG00000092931.12 | transcript | ENST00000685175.1 | protein_coding | 8/12 | chr17 | 76759634 | |||||||
| chr17:76759670 | G | A | 2 | a0001c0006t0007g0042 a0001c0006t0007g0043 |
2 | HG02602.hp1 HG02735.hp1 |
intron_variant | MODIFIER | c.682+5583G>A | MFSD11 | ENSG00000092931.12 | transcript | ENST00000685175.1 | protein_coding | 8/12 | chr17 | 76759670 | |||||||
| chr17:76759681 | T | C | 7 | a0001c0001t0004g0012 a0001c0001t0004g0030 a0001c0001t0004g0031 others(4): Show |
7 | HG01069.hp1 HG02258.hp2 HG02630.hp2 others(4): Show |
intron_variant | MODIFIER | c.682+5594T>C | MFSD11 | ENSG00000092931.12 | transcript | ENST00000685175.1 | protein_coding | 8/12 | chr17 | 76759681 | |||||||
| chr17:76759756 | C | CT | 70 | a0001c0001t0001g0010 a0001c0001t0001g0050 a0001c0001t0001g0051 others(67): Show |
74 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(71): Show |
intron_variant | MODIFIER | c.682+5699dupT | MFSD11 | ENSG00000092931.12 | transcript | ENST00000685175.1 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr17 | 76759756 | ||||||
| chr17:76759756 | C | CTT | 86 | a0001c0001t0001g0007 a0001c0001t0001g0046 a0001c0001t0001g0047 others(83): Show |
87 | HG00140.hp1 HG00280.hp1 HG00423.hp1 others(84): Show |
intron_variant | MODIFIER | c.682+5698_682+5699d others(4): Show |
MFSD11 | ENSG00000092931.12 | transcript | ENST00000685175.1 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr17 | 76759756 | ||||||
| chr17:76759756 | C | CTTT | 34 | a0001c0001t0001g0069 a0001c0001t0001g0087 a0001c0001t0001g0128 others(31): Show |
34 | HG00099.hp1 HG00423.hp2 HG00544.hp2 others(31): Show |
intron_variant | MODIFIER | c.682+5697_682+5699d others(5): Show |
MFSD11 | ENSG00000092931.12 | transcript | ENST00000685175.1 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr17 | 76759756 | ||||||
| chr17:76759756 | CT | C | 10 | a0001c0001t0001g0139 a0001c0001t0001g0148 a0001c0001t0003g0013 others(7): Show |
10 | HG02886.hp2 HG02922.hp2 HG02976.hp1 others(7): Show |
intron_variant | MODIFIER | c.682+5699delT | MFSD11 | ENSG00000092931.12 | transcript | ENST00000685175.1 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr17 | 76759756 | ||||||
| chr17:76759756 | CTTT | C | 18 | a0001c0001t0002g0006 a0001c0001t0002g0071 a0001c0001t0002g0081 others(15): Show |
19 | HG00609.hp1 HG00621.hp1 HG01361.hp2 others(16): Show |
intron_variant | MODIFIER | c.682+5697_682+5699d others(5): Show |
MFSD11 | ENSG00000092931.12 | transcript | ENST00000685175.1 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr17 | 76759756 | ||||||
| chr17:76759756 | CTTTT | C | 29 | a0001c0001t0001g0323 a0001c0001t0002g0002 a0001c0001t0002g0005 others(26): Show |
32 | HG00140.hp2 HG00558.hp1 HG00597.hp2 others(29): Show |
intron_variant | MODIFIER | c.682+5696_682+5699d others(6): Show |
MFSD11 | ENSG00000092931.12 | transcript | ENST00000685175.1 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr17 | 76759756 | ||||||
| chr17:76759756 | CTTTTTTT others(3): Show |
C | 4 | a0001c0001t0001g0098 a0001c0001t0001g0300 a0001c0001t0001g0327 others(1): Show |
4 | HG01243.hp1 HG02572.hp2 HG04184.hp2 others(1): Show |
intron_variant | MODIFIER | c.682+5690_682+5699d others(12): Show |
MFSD11 | ENSG00000092931.12 | transcript | ENST00000685175.1 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr17 | 76759756 | ||||||
| chr17:76759756 | CTTTTTTT others(4): Show |
C | 21 | a0001c0001t0001g0003 a0001c0001t0001g0044 a0001c0001t0001g0157 others(18): Show |
22 | HG00673.hp1 HG01074.hp2 HG01123.hp2 others(19): Show |
intron_variant | MODIFIER | c.682+5689_682+5699d others(13): Show |
MFSD11 | ENSG00000092931.12 | transcript | ENST00000685175.1 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr17 | 76759756 | ||||||
| chr17:76759756 | CTTTTTTT others(8): Show |
C | 2 | a0001c0006t0007g0042 a0001c0006t0007g0043 |
2 | HG02602.hp1 HG02735.hp1 |
intron_variant | MODIFIER | c.682+5685_682+5699d others(17): Show |
MFSD11 | ENSG00000092931.12 | transcript | ENST00000685175.1 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr17 | 76759756 | ||||||
| chr17:76759775 | T | G | 1 | a0001c0001t0002g0165 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.682+5688T>G | MFSD11 | ENSG00000092931.12 | transcript | ENST00000685175.1 | protein_coding | 8/12 | chr17 | 76759775 | |||||||
| chr17:76759825 | G | A | 2 | a0001c0006t0007g0042 a0001c0006t0007g0043 |
2 | HG02602.hp1 HG02735.hp1 |
intron_variant | MODIFIER | c.682+5738G>A | MFSD11 | ENSG00000092931.12 | transcript | ENST00000685175.1 | protein_coding | 8/12 | chr17 | 76759825 | |||||||
| chr17:76759939 | T | C | 1 | a0001c0001t0001g0151 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.682+5852T>C | MFSD11 | ENSG00000092931.12 | transcript | ENST00000685175.1 | protein_coding | 8/12 | chr17 | 76759939 | |||||||
| chr17:76759980 | T | C | 2 | a0001c0006t0007g0042 a0001c0006t0007g0043 |
2 | HG02602.hp1 HG02735.hp1 |
intron_variant | MODIFIER | c.682+5893T>C | MFSD11 | ENSG00000092931.12 | transcript | ENST00000685175.1 | protein_coding | 8/12 | chr17 | 76759980 | |||||||
| chr17:76759994 | C | A | 329 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0010 others(326): Show |
342 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(339): Show |
intron_variant | MODIFIER | c.682+5907C>A | MFSD11 | ENSG00000092931.12 | transcript | ENST00000685175.1 | protein_coding | 8/12 | chr17 | 76759994 | |||||||
| chr17:76760006 | T | G | 2 | a0001c0006t0007g0042 a0001c0006t0007g0043 |
2 | HG02602.hp1 HG02735.hp1 |
intron_variant | MODIFIER | c.682+5919T>G | MFSD11 | ENSG00000092931.12 | transcript | ENST00000685175.1 | protein_coding | 8/12 | chr17 | 76760006 | |||||||
| chr17:76760065 | C | T | 6 | a0001c0001t0001g0105 a0001c0001t0001g0130 a0001c0001t0006g0325 others(3): Show |
6 | HG01099.hp1 HG01884.hp2 HG02145.hp2 others(3): Show |
intron_variant | MODIFIER | c.682+5978C>T | MFSD11 | ENSG00000092931.12 | transcript | ENST00000685175.1 | protein_coding | 8/12 | chr17 | 76760065 | |||||||
| chr17:76760082 | G | A | 329 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0010 others(326): Show |
342 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(339): Show |
intron_variant | MODIFIER | c.682+5995G>A | MFSD11 | ENSG00000092931.12 | transcript | ENST00000685175.1 | protein_coding | 8/12 | chr17 | 76760082 | |||||||
| chr17:76760089 | G | A | 6 | a0001c0001t0004g0012 a0001c0001t0004g0030 a0001c0001t0004g0031 others(3): Show |
6 | HG01069.hp1 HG02258.hp2 HG02630.hp2 others(3): Show |
intron_variant | MODIFIER | c.682+6002G>A | MFSD11 | ENSG00000092931.12 | transcript | ENST00000685175.1 | protein_coding | 8/12 | chr17 | 76760089 | |||||||
| chr17:76760097 | G | A | 3 | a0001c0001t0001g0225 a0001c0001t0001g0230 a0001c0001t0001g0238 |
3 | HG01169.hp2 HG01517.hp2 HG02486.hp1 |
intron_variant | MODIFIER | c.682+6010G>A | MFSD11 | ENSG00000092931.12 | transcript | ENST00000685175.1 | protein_coding | 8/12 | chr17 | 76760097 | |||||||
| chr17:76760139 | G | A | 11 | a0001c0001t0001g0129 a0001c0001t0001g0147 a0001c0001t0001g0148 others(8): Show |
11 | HG01891.hp2 HG02622.hp1 HG02818.hp1 others(8): Show |
intron_variant | MODIFIER | c.682+6052G>A | MFSD11 | ENSG00000092931.12 | transcript | ENST00000685175.1 | protein_coding | 8/12 | chr17 | 76760139 | |||||||
| chr17:76760140 | C | T | 6 | a0001c0001t0001g0105 a0001c0001t0001g0130 a0001c0001t0006g0325 others(3): Show |
6 | HG01099.hp1 HG01884.hp2 HG02145.hp2 others(3): Show |
intron_variant | MODIFIER | c.682+6053C>T | MFSD11 | ENSG00000092931.12 | transcript | ENST00000685175.1 | protein_coding | 8/12 | chr17 | 76760140 | |||||||
| chr17:76760145 | A | G | 2 | a0001c0006t0007g0042 a0001c0006t0007g0043 |
2 | HG02602.hp1 HG02735.hp1 |
intron_variant | MODIFIER | c.682+6058A>G | MFSD11 | ENSG00000092931.12 | transcript | ENST00000685175.1 | protein_coding | 8/12 | chr17 | 76760145 | |||||||
| chr17:76760180 | A | G | 2 | a0001c0006t0007g0042 a0001c0006t0007g0043 |
2 | HG02602.hp1 HG02735.hp1 |
intron_variant | MODIFIER | c.682+6093A>G | MFSD11 | ENSG00000092931.12 | transcript | ENST00000685175.1 | protein_coding | 8/12 | chr17 | 76760180 | |||||||
| chr17:76760277 | C | CA | 11 | a0001c0001t0001g0101 a0001c0001t0001g0259 a0001c0001t0002g0096 others(8): Show |
11 | HG01069.hp1 HG02258.hp2 HG02602.hp1 others(8): Show |
intron_variant | MODIFIER | c.682+6205dupA | MFSD11 | ENSG00000092931.12 | transcript | ENST00000685175.1 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr17 | 76760277 | ||||||
| chr17:76760439 | C | T | 2 | a0001c0006t0007g0042 a0001c0006t0007g0043 |
2 | HG02602.hp1 HG02735.hp1 |
intron_variant | MODIFIER | c.682+6352C>T | MFSD11 | ENSG00000092931.12 | transcript | ENST00000685175.1 | protein_coding | 8/12 | chr17 | 76760439 | |||||||
| chr17:76760475 | T | G | 1 | a0001c0001t0001g0324 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.682+6388T>G | MFSD11 | ENSG00000092931.12 | transcript | ENST00000685175.1 | protein_coding | 8/12 | chr17 | 76760475 | |||||||
| chr17:76760482 | G | C | 1 | a0001c0001t0013g0132 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.682+6395G>C | MFSD11 | ENSG00000092931.12 | transcript | ENST00000685175.1 | protein_coding | 8/12 | chr17 | 76760482 | |||||||
| chr17:76760503 | T | G | 2 | a0001c0006t0007g0042 a0001c0006t0007g0043 |
2 | HG02602.hp1 HG02735.hp1 |
intron_variant | MODIFIER | c.682+6416T>G | MFSD11 | ENSG00000092931.12 | transcript | ENST00000685175.1 | protein_coding | 8/12 | chr17 | 76760503 | |||||||
| chr17:76760527 | C | CT | 37 | a0001c0001t0001g0105 a0001c0001t0001g0129 a0001c0001t0001g0130 others(34): Show |
38 | HG01069.hp1 HG01099.hp1 HG01243.hp1 others(35): Show |
intron_variant | MODIFIER | c.682+6452dupT | MFSD11 | ENSG00000092931.12 | transcript | ENST00000685175.1 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr17 | 76760527 | ||||||
| chr17:76760543 | C | T | 2 | a0001c0001t0002g0211 a0001c0001t0002g0247 |
2 | NA18944.hp2 NA18983.hp2 |
intron_variant | MODIFIER | c.682+6456C>T | MFSD11 | ENSG00000092931.12 | transcript | ENST00000685175.1 | protein_coding | 8/12 | chr17 | 76760543 | |||||||
| chr17:76760547 | G | A | 1 | a0001c0001t0001g0146 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.682+6460G>A | MFSD11 | ENSG00000092931.12 | transcript | ENST00000685175.1 | protein_coding | 8/12 | chr17 | 76760547 | |||||||
| chr17:76760552 | G | A | 1 | a0001c0001t0001g0051 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.682+6465G>A | MFSD11 | ENSG00000092931.12 | transcript | ENST00000685175.1 | protein_coding | 8/12 | chr17 | 76760552 | |||||||
| chr17:76760600 | G | A | 1 | a0001c0001t0001g0308 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.682+6513G>A | MFSD11 | ENSG00000092931.12 | transcript | ENST00000685175.1 | protein_coding | 8/12 | chr17 | 76760600 | |||||||
| chr17:76760712 | G | A | 6 | a0001c0001t0001g0047 a0001c0001t0001g0048 a0001c0001t0001g0050 others(3): Show |
6 | HG00544.hp1 NA18971.hp1 NA18979.hp2 others(3): Show |
intron_variant | MODIFIER | c.682+6625G>A | MFSD11 | ENSG00000092931.12 | transcript | ENST00000685175.1 | protein_coding | 8/12 | chr17 | 76760712 | |||||||
| chr17:76760784 | G | A | 2 | a0001c0006t0007g0042 a0001c0006t0007g0043 |
2 | HG02602.hp1 HG02735.hp1 |
intron_variant | MODIFIER | c.683-6602G>A | MFSD11 | ENSG00000092931.12 | transcript | ENST00000685175.1 | protein_coding | 8/12 | chr17 | 76760784 | |||||||
| chr17:76760796 | T | G | 2 | a0001c0006t0007g0042 a0001c0006t0007g0043 |
2 | HG02602.hp1 HG02735.hp1 |
intron_variant | MODIFIER | c.683-6590T>G | MFSD11 | ENSG00000092931.12 | transcript | ENST00000685175.1 | protein_coding | 8/12 | chr17 | 76760796 | |||||||
| chr17:76760885 | C | G | 1 | a0001c0001t0002g0248 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.683-6501C>G | MFSD11 | ENSG00000092931.12 | transcript | ENST00000685175.1 | protein_coding | 8/12 | chr17 | 76760885 | |||||||
| chr17:76760886 | G | C | 1 | a0001c0001t0002g0248 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.683-6500G>C | MFSD11 | ENSG00000092931.12 | transcript | ENST00000685175.1 | protein_coding | 8/12 | chr17 | 76760886 | |||||||
| chr17:76760887 | G | T | 1 | a0001c0001t0002g0248 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.683-6499G>T | MFSD11 | ENSG00000092931.12 | transcript | ENST00000685175.1 | protein_coding | 8/12 | chr17 | 76760887 | |||||||
| chr17:76760969 | G | T | 2 | a0001c0001t0001g0226 a0001c0001t0001g0318 |
2 | HG00735.hp1 HG01106.hp1 |
intron_variant | MODIFIER | c.683-6417G>T | MFSD11 | ENSG00000092931.12 | transcript | ENST00000685175.1 | protein_coding | 8/12 | chr17 | 76760969 | |||||||
| chr17:76760980 | C | T | 1 | a0001c0001t0001g0261 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.683-6406C>T | MFSD11 | ENSG00000092931.12 | transcript | ENST00000685175.1 | protein_coding | 8/12 | chr17 | 76760980 | |||||||
| chr17:76761062 | G | A | 45 | a0001c0001t0001g0003 a0001c0001t0001g0010 a0001c0001t0001g0044 others(42): Show |
47 | HG00639.hp2 HG00673.hp1 HG01069.hp2 others(44): Show |
intron_variant | MODIFIER | c.683-6324G>A | MFSD11 | ENSG00000092931.12 | transcript | ENST00000685175.1 | protein_coding | 8/12 | chr17 | 76761062 | |||||||
| chr17:76761067 | C | T | 11 | a0001c0001t0002g0001 a0001c0001t0002g0008 a0001c0001t0002g0190 others(8): Show |
15 | HG00280.hp2 NA18944.hp2 NA18948.hp2 others(12): Show |
intron_variant | MODIFIER | c.683-6319C>T | MFSD11 | ENSG00000092931.12 | transcript | ENST00000685175.1 | protein_coding | 8/12 | chr17 | 76761067 | |||||||
| chr17:76761154 | G | A | 2 | a0001c0006t0007g0042 a0001c0006t0007g0043 |
2 | HG02602.hp1 HG02735.hp1 |
intron_variant | MODIFIER | c.683-6232G>A | MFSD11 | ENSG00000092931.12 | transcript | ENST00000685175.1 | protein_coding | 8/12 | chr17 | 76761154 | |||||||
| chr17:76761516 | A | G | 5 | a0001c0001t0005g0035 a0001c0001t0005g0036 a0001c0001t0005g0037 others(2): Show |
5 | HG02630.hp1 HG02886.hp2 HG03209.hp1 others(2): Show |
intron_variant | MODIFIER | c.683-5870A>G | MFSD11 | ENSG00000092931.12 | transcript | ENST00000685175.1 | protein_coding | 8/12 | chr17 | 76761516 | |||||||
| chr17:76761564 | A | G | 2 | a0001c0006t0007g0042 a0001c0006t0007g0043 |
2 | HG02602.hp1 HG02735.hp1 |
intron_variant | MODIFIER | c.683-5822A>G | MFSD11 | ENSG00000092931.12 | transcript | ENST00000685175.1 | protein_coding | 8/12 | chr17 | 76761564 | |||||||
| chr17:76761628 | T | C | 1 | a0001c0001t0001g0161 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.683-5758T>C | MFSD11 | ENSG00000092931.12 | transcript | ENST00000685175.1 | protein_coding | 8/12 | chr17 | 76761628 | |||||||
| chr17:76761645 | G | A | 3 | a0001c0001t0001g0130 a0001c0004t0001g0100 a0001c0004t0001g0131 |
3 | HG02145.hp2 NA18522.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.683-5741G>A | MFSD11 | ENSG00000092931.12 | transcript | ENST00000685175.1 | protein_coding | 8/12 | chr17 | 76761645 | |||||||
| chr17:76761698 | G | A | 1 | a0001c0001t0001g0162 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.683-5688G>A | MFSD11 | ENSG00000092931.12 | transcript | ENST00000685175.1 | protein_coding | 8/12 | chr17 | 76761698 | |||||||
| chr17:76761738 | T | C | 2 | a0001c0006t0007g0042 a0001c0006t0007g0043 |
2 | HG02602.hp1 HG02735.hp1 |
intron_variant | MODIFIER | c.683-5648T>C | MFSD11 | ENSG00000092931.12 | transcript | ENST00000685175.1 | protein_coding | 8/12 | chr17 | 76761738 | |||||||
| chr17:76761869 | C | T | 2 | a0001c0006t0007g0042 a0001c0006t0007g0043 |
2 | HG02602.hp1 HG02735.hp1 |
intron_variant | MODIFIER | c.683-5517C>T | MFSD11 | ENSG00000092931.12 | transcript | ENST00000685175.1 | protein_coding | 8/12 | chr17 | 76761869 | |||||||
| chr17:76761915 | C | T | 2 | a0001c0001t0001g0279 a0002c0007t0001g0280 |
2 | HG02257.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.683-5471C>T | MFSD11 | ENSG00000092931.12 | transcript | ENST00000685175.1 | protein_coding | 8/12 | chr17 | 76761915 | |||||||
| chr17:76761920 | C | CA | 14 | a0001c0001t0001g0098 a0001c0001t0001g0332 a0001c0001t0001g0334 others(11): Show |
14 | HG01361.hp2 HG02071.hp1 HG02630.hp1 others(11): Show |
intron_variant | MODIFIER | c.683-5450dupA | MFSD11 | ENSG00000092931.12 | transcript | ENST00000685175.1 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr17 | 76761920 | ||||||
| chr17:76762018 | G | A | 2 | a0001c0001t0002g0245 a0001c0001t0002g0294 |
2 | NA18977.hp1 NA18981.hp2 |
intron_variant | MODIFIER | c.683-5368G>A | MFSD11 | ENSG00000092931.12 | transcript | ENST00000685175.1 | protein_coding | 8/12 | chr17 | 76762018 | |||||||
| chr17:76762119 | A | G | 1 | a0001c0001t0001g0234 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.683-5267A>G | MFSD11 | ENSG00000092931.12 | transcript | ENST00000685175.1 | protein_coding | 8/12 | chr17 | 76762119 | |||||||
| chr17:76762146 | C | A | 2 | a0001c0006t0007g0042 a0001c0006t0007g0043 |
2 | HG02602.hp1 HG02735.hp1 |
intron_variant | MODIFIER | c.683-5240C>A | MFSD11 | ENSG00000092931.12 | transcript | ENST00000685175.1 | protein_coding | 8/12 | chr17 | 76762146 | |||||||
| chr17:76762435 | C | T | 2 | a0001c0006t0007g0042 a0001c0006t0007g0043 |
2 | HG02602.hp1 HG02735.hp1 |
intron_variant | MODIFIER | c.683-4951C>T | MFSD11 | ENSG00000092931.12 | transcript | ENST00000685175.1 | protein_coding | 8/12 | chr17 | 76762435 | |||||||
| chr17:76762514 | A | G | 2 | a0001c0006t0007g0042 a0001c0006t0007g0043 |
2 | HG02602.hp1 HG02735.hp1 |
intron_variant | MODIFIER | c.683-4872A>G | MFSD11 | ENSG00000092931.12 | transcript | ENST00000685175.1 | protein_coding | 8/12 | chr17 | 76762514 | |||||||
| chr17:76762536 | G | A | 286 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0010 others(283): Show |
298 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(295): Show |
intron_variant | MODIFIER | c.683-4850G>A | MFSD11 | ENSG00000092931.12 | transcript | ENST00000685175.1 | protein_coding | 8/12 | chr17 | 76762536 | |||||||
| chr17:76762634 | C | T | 3 | a0001c0001t0001g0105 a0001c0001t0006g0325 a0001c0001t0006g0326 |
3 | HG01099.hp1 HG01884.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.683-4752C>T | MFSD11 | ENSG00000092931.12 | transcript | ENST00000685175.1 | protein_coding | 8/12 | chr17 | 76762634 | |||||||
| chr17:76762656 | CA | C | 279 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0010 others(276): Show |
292 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(289): Show |
intron_variant | MODIFIER | c.683-4710delA | MFSD11 | ENSG00000092931.12 | transcript | ENST00000685175.1 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr17 | 76762656 | ||||||
| chr17:76762714 | G | C | 1 | a0001c0001t0003g0022 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.683-4672G>C | MFSD11 | ENSG00000092931.12 | transcript | ENST00000685175.1 | protein_coding | 8/12 | chr17 | 76762714 | |||||||
| chr17:76762753 | G | A | 1 | a0001c0001t0001g0277 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.683-4633G>A | MFSD11 | ENSG00000092931.12 | transcript | ENST00000685175.1 | protein_coding | 8/12 | chr17 | 76762753 | |||||||
| chr17:76762850 | T | A | 37 | a0001c0001t0001g0105 a0001c0001t0001g0129 a0001c0001t0001g0130 others(34): Show |
38 | HG01069.hp1 HG01099.hp1 HG01243.hp1 others(35): Show |
intron_variant | MODIFIER | c.683-4536T>A | MFSD11 | ENSG00000092931.12 | transcript | ENST00000685175.1 | protein_coding | 8/12 | chr17 | 76762850 | |||||||
| chr17:76762887 | A | T | 2 | a0001c0006t0007g0042 a0001c0006t0007g0043 |
2 | HG02602.hp1 HG02735.hp1 |
intron_variant | MODIFIER | c.683-4499A>T | MFSD11 | ENSG00000092931.12 | transcript | ENST00000685175.1 | protein_coding | 8/12 | chr17 | 76762887 | |||||||
| chr17:76762974 | T | C | 2 | a0001c0001t0001g0279 a0002c0007t0001g0280 |
2 | HG02257.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.683-4412T>C | MFSD11 | ENSG00000092931.12 | transcript | ENST00000685175.1 | protein_coding | 8/12 | chr17 | 76762974 | |||||||
| chr17:76763006 | C | T | 2 | a0001c0006t0007g0042 a0001c0006t0007g0043 |
2 | HG02602.hp1 HG02735.hp1 |
intron_variant | MODIFIER | c.683-4380C>T | MFSD11 | ENSG00000092931.12 | transcript | ENST00000685175.1 | protein_coding | 8/12 | chr17 | 76763006 | |||||||
| chr17:76763044 | C | G | 34 | a0001c0001t0001g0105 a0001c0001t0001g0129 a0001c0001t0001g0130 others(31): Show |
35 | HG01069.hp1 HG01099.hp1 HG01243.hp1 others(32): Show |
intron_variant | MODIFIER | c.683-4342C>G | MFSD11 | ENSG00000092931.12 | transcript | ENST00000685175.1 | protein_coding | 8/12 | chr17 | 76763044 | |||||||
| chr17:76763082 | G | A | 6 | a0001c0001t0001g0105 a0001c0001t0001g0130 a0001c0001t0006g0325 others(3): Show |
6 | HG01099.hp1 HG01884.hp2 HG02145.hp2 others(3): Show |
intron_variant | MODIFIER | c.683-4304G>A | MFSD11 | ENSG00000092931.12 | transcript | ENST00000685175.1 | protein_coding | 8/12 | chr17 | 76763082 | |||||||
| chr17:76763102 | C | A | 2 | a0001c0006t0007g0042 a0001c0006t0007g0043 |
2 | HG02602.hp1 HG02735.hp1 |
intron_variant | MODIFIER | c.683-4284C>A | MFSD11 | ENSG00000092931.12 | transcript | ENST00000685175.1 | protein_coding | 8/12 | chr17 | 76763102 | |||||||
| chr17:76763182 | T | G | 3 | a0001c0001t0001g0332 a0001c0001t0001g0334 a0001c0001t0001g0335 |
3 | HG03453.hp1 HG03516.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.683-4204T>G | MFSD11 | ENSG00000092931.12 | transcript | ENST00000685175.1 | protein_coding | 8/12 | chr17 | 76763182 | |||||||
| chr17:76763237 | G | A | 1 | a0001c0001t0003g0011 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.683-4149G>A | MFSD11 | ENSG00000092931.12 | transcript | ENST00000685175.1 | protein_coding | 8/12 | chr17 | 76763237 | |||||||
| chr17:76763270 | T | G | 1 | a0001c0001t0003g0023 | 1 | NA19075.hp2 | intron_variant | MODIFIER | c.683-4116T>G | MFSD11 | ENSG00000092931.12 | transcript | ENST00000685175.1 | protein_coding | 8/12 | chr17 | 76763270 | |||||||
| chr17:76763271 | G | GT | 7 | a0001c0001t0001g0285 a0001c0001t0001g0290 a0001c0001t0001g0291 others(4): Show |
7 | HG01891.hp1 HG02572.hp2 HG02809.hp1 others(4): Show |
intron_variant | MODIFIER | c.683-4104dupT | MFSD11 | ENSG00000092931.12 | transcript | ENST00000685175.1 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr17 | 76763271 | ||||||
| chr17:76763516 | A | G | 11 | a0001c0001t0002g0001 a0001c0001t0002g0008 a0001c0001t0002g0190 others(8): Show |
15 | HG00280.hp2 NA18944.hp2 NA18948.hp2 others(12): Show |
intron_variant | MODIFIER | c.683-3870A>G | MFSD11 | ENSG00000092931.12 | transcript | ENST00000685175.1 | protein_coding | 8/12 | chr17 | 76763516 | |||||||
| chr17:76763560 | G | A | 4 | a0001c0002t0001g0004 a0001c0002t0001g0074 a0001c0002t0001g0075 others(1): Show |
5 | HG01243.hp1 HG01884.hp1 HG02622.hp2 others(2): Show |
intron_variant | MODIFIER | c.683-3826G>A | MFSD11 | ENSG00000092931.12 | transcript | ENST00000685175.1 | protein_coding | 8/12 | chr17 | 76763560 | |||||||
| chr17:76763702 | C | G | 1 | a0001c0001t0001g0138 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.683-3684C>G | MFSD11 | ENSG00000092931.12 | transcript | ENST00000685175.1 | protein_coding | 8/12 | chr17 | 76763702 | |||||||
| chr17:76763729 | C | T | 6 | a0001c0001t0001g0105 a0001c0001t0001g0130 a0001c0001t0006g0325 others(3): Show |
6 | HG01099.hp1 HG01884.hp2 HG02145.hp2 others(3): Show |
intron_variant | MODIFIER | c.683-3657C>T | MFSD11 | ENSG00000092931.12 | transcript | ENST00000685175.1 | protein_coding | 8/12 | chr17 | 76763729 | |||||||
| chr17:76763735 | A | G | 2 | a0001c0006t0007g0042 a0001c0006t0007g0043 |
2 | HG02602.hp1 HG02735.hp1 |
intron_variant | MODIFIER | c.683-3651A>G | MFSD11 | ENSG00000092931.12 | transcript | ENST00000685175.1 | protein_coding | 8/12 | chr17 | 76763735 | |||||||
| chr17:76763858 | G | A | 1 | a0001c0001t0001g0232 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.683-3528G>A | MFSD11 | ENSG00000092931.12 | transcript | ENST00000685175.1 | protein_coding | 8/12 | chr17 | 76763858 | |||||||
| chr17:76763876 | T | G | 1 | a0001c0001t0002g0220 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.683-3510T>G | MFSD11 | ENSG00000092931.12 | transcript | ENST00000685175.1 | protein_coding | 8/12 | chr17 | 76763876 | |||||||
| chr17:76763965 | C | T | 2 | a0001c0006t0007g0042 a0001c0006t0007g0043 |
2 | HG02602.hp1 HG02735.hp1 |
intron_variant | MODIFIER | c.683-3421C>T | MFSD11 | ENSG00000092931.12 | transcript | ENST00000685175.1 | protein_coding | 8/12 | chr17 | 76763965 | |||||||
| chr17:76763966 | A | G | 35 | a0001c0001t0001g0105 a0001c0001t0001g0129 a0001c0001t0001g0130 others(32): Show |
36 | HG01069.hp1 HG01099.hp1 HG01243.hp1 others(33): Show |
intron_variant | MODIFIER | c.683-3420A>G | MFSD11 | ENSG00000092931.12 | transcript | ENST00000685175.1 | protein_coding | 8/12 | chr17 | 76763966 | |||||||
| chr17:76764102 | C | A | 1 | a0001c0001t0002g0120 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.683-3284C>A | MFSD11 | ENSG00000092931.12 | transcript | ENST00000685175.1 | protein_coding | 8/12 | chr17 | 76764102 | |||||||
| chr17:76764236 | TTATC | T | 6 | a0001c0001t0001g0105 a0001c0001t0001g0130 a0001c0001t0006g0325 others(3): Show |
6 | HG01099.hp1 HG01884.hp2 HG02145.hp2 others(3): Show |
intron_variant | MODIFIER | c.683-3148_683-3145d others(6): Show |
MFSD11 | ENSG00000092931.12 | transcript | ENST00000685175.1 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr17 | 76764236 | ||||||
| chr17:76764270 | A | G | 1 | a0001c0001t0001g0335 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.683-3116A>G | MFSD11 | ENSG00000092931.12 | transcript | ENST00000685175.1 | protein_coding | 8/12 | chr17 | 76764270 | |||||||
| chr17:76764310 | TGTTA | T | 9 | a0001c0001t0005g0035 a0001c0001t0005g0036 a0001c0001t0005g0037 others(6): Show |
10 | HG01243.hp1 HG01884.hp1 HG02622.hp2 others(7): Show |
intron_variant | MODIFIER | c.683-3075_683-3072d others(6): Show |
MFSD11 | ENSG00000092931.12 | transcript | ENST00000685175.1 | protein_coding | 8/12 | chr17 | 76764310 | |||||||
| chr17:76764315 | T | A | 9 | a0001c0001t0005g0035 a0001c0001t0005g0036 a0001c0001t0005g0037 others(6): Show |
10 | HG01243.hp1 HG01884.hp1 HG02622.hp2 others(7): Show |
intron_variant | MODIFIER | c.683-3071T>A | MFSD11 | ENSG00000092931.12 | transcript | ENST00000685175.1 | protein_coding | 8/12 | chr17 | 76764315 | |||||||
| chr17:76764349 | C | T | 1 | a0001c0001t0001g0179 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.683-3037C>T | MFSD11 | ENSG00000092931.12 | transcript | ENST00000685175.1 | protein_coding | 8/12 | chr17 | 76764349 | |||||||
| chr17:76764372 | C | T | 1 | a0001c0001t0001g0070 | 1 | NA18991.hp2 | intron_variant | MODIFIER | c.683-3014C>T | MFSD11 | ENSG00000092931.12 | transcript | ENST00000685175.1 | protein_coding | 8/12 | chr17 | 76764372 | |||||||
| chr17:76764431 | A | G | 2 | a0001c0001t0001g0170 a0004c0010t0001g0169 |
2 | HG00673.hp1 NA18943.hp1 |
intron_variant | MODIFIER | c.683-2955A>G | MFSD11 | ENSG00000092931.12 | transcript | ENST00000685175.1 | protein_coding | 8/12 | chr17 | 76764431 | |||||||
| chr17:76764575 | G | A | 2 | a0001c0006t0007g0042 a0001c0006t0007g0043 |
2 | HG02602.hp1 HG02735.hp1 |
intron_variant | MODIFIER | c.683-2811G>A | MFSD11 | ENSG00000092931.12 | transcript | ENST00000685175.1 | protein_coding | 8/12 | chr17 | 76764575 | |||||||
| chr17:76764608 | C | T | 1 | a0001c0001t0003g0011 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.683-2778C>T | MFSD11 | ENSG00000092931.12 | transcript | ENST00000685175.1 | protein_coding | 8/12 | chr17 | 76764608 | |||||||
| chr17:76764656 | G | C | 2 | a0001c0001t0006g0325 a0001c0001t0006g0326 |
2 | HG01099.hp1 HG01884.hp2 |
intron_variant | MODIFIER | c.683-2730G>C | MFSD11 | ENSG00000092931.12 | transcript | ENST00000685175.1 | protein_coding | 8/12 | chr17 | 76764656 | |||||||
| chr17:76764686 | T | TAC | 8 | a0001c0001t0001g0103 a0001c0001t0001g0161 a0001c0001t0001g0328 others(5): Show |
8 | HG00639.hp2 HG02109.hp2 HG02602.hp1 others(5): Show |
intron_variant | MODIFIER | c.683-2682_683-2681d others(4): Show |
MFSD11 | ENSG00000092931.12 | transcript | ENST00000685175.1 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr17 | 76764686 | ||||||
| chr17:76764686 | TAC | T | 23 | a0001c0001t0001g0105 a0001c0001t0001g0129 a0001c0001t0001g0130 others(20): Show |
23 | HG01069.hp1 HG01099.hp1 HG01884.hp2 others(20): Show |
intron_variant | MODIFIER | c.683-2682_683-2681d others(4): Show |
MFSD11 | ENSG00000092931.12 | transcript | ENST00000685175.1 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr17 | 76764686 | ||||||
| chr17:76764747 | A | G | 5 | a0001c0001t0005g0035 a0001c0001t0005g0036 a0001c0001t0005g0037 others(2): Show |
5 | HG02630.hp1 HG02886.hp2 HG03209.hp1 others(2): Show |
intron_variant | MODIFIER | c.683-2639A>G | MFSD11 | ENSG00000092931.12 | transcript | ENST00000685175.1 | protein_coding | 8/12 | chr17 | 76764747 | |||||||
| chr17:76764880 | C | T | 4 | a0001c0001t0001g0047 a0001c0001t0001g0050 a0001c0001t0001g0051 others(1): Show |
4 | NA18971.hp1 NA18979.hp2 NA18984.hp2 others(1): Show |
intron_variant | MODIFIER | c.683-2506C>T | MFSD11 | ENSG00000092931.12 | transcript | ENST00000685175.1 | protein_coding | 8/12 | chr17 | 76764880 | |||||||
| chr17:76765116 | T | C | 47 | a0001c0001t0001g0105 a0001c0001t0001g0129 a0001c0001t0001g0130 others(44): Show |
48 | HG01069.hp1 HG01099.hp1 HG01106.hp2 others(45): Show |
intron_variant | MODIFIER | c.683-2270T>C | MFSD11 | ENSG00000092931.12 | transcript | ENST00000685175.1 | protein_coding | 8/12 | chr17 | 76765116 | |||||||
| chr17:76765154 | T | C | 2 | a0001c0006t0007g0042 a0001c0006t0007g0043 |
2 | HG02602.hp1 HG02735.hp1 |
intron_variant | MODIFIER | c.683-2232T>C | MFSD11 | ENSG00000092931.12 | transcript | ENST00000685175.1 | protein_coding | 8/12 | chr17 | 76765154 | |||||||
| chr17:76765225 | A | G | 1 | a0001c0001t0001g0003 | 2 | NA20752.hp1 NA20805.hp2 |
intron_variant | MODIFIER | c.683-2161A>G | MFSD11 | ENSG00000092931.12 | transcript | ENST00000685175.1 | protein_coding | 8/12 | chr17 | 76765225 | |||||||
| chr17:76765241 | A | G | 2 | a0001c0006t0007g0042 a0001c0006t0007g0043 |
2 | HG02602.hp1 HG02735.hp1 |
intron_variant | MODIFIER | c.683-2145A>G | MFSD11 | ENSG00000092931.12 | transcript | ENST00000685175.1 | protein_coding | 8/12 | chr17 | 76765241 | |||||||
| chr17:76765251 | C | T | 2 | a0001c0006t0007g0042 a0001c0006t0007g0043 |
2 | HG02602.hp1 HG02735.hp1 |
intron_variant | MODIFIER | c.683-2135C>T | MFSD11 | ENSG00000092931.12 | transcript | ENST00000685175.1 | protein_coding | 8/12 | chr17 | 76765251 | |||||||
| chr17:76765258 | G | A | 3 | a0001c0001t0001g0328 a0001c0001t0001g0329 a0001c0001t0001g0333 |
3 | HG03098.hp2 HG03209.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.683-2128G>A | MFSD11 | ENSG00000092931.12 | transcript | ENST00000685175.1 | protein_coding | 8/12 | chr17 | 76765258 | |||||||
| chr17:76765278 | T | C | 2 | a0001c0001t0001g0306 a0001c0001t0001g0307 |
2 | NA18965.hp2 NA18971.hp2 |
intron_variant | MODIFIER | c.683-2108T>C | MFSD11 | ENSG00000092931.12 | transcript | ENST00000685175.1 | protein_coding | 8/12 | chr17 | 76765278 | |||||||
| chr17:76765452 | C | CT | 72 | a0001c0001t0001g0047 a0001c0001t0001g0048 a0001c0001t0001g0053 others(69): Show |
72 | HG00140.hp1 HG00140.hp2 HG00423.hp1 others(69): Show |
intron_variant | MODIFIER | c.683-1906dupT | MFSD11 | ENSG00000092931.12 | transcript | ENST00000685175.1 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr17 | 76765452 | ||||||
| chr17:76765452 | C | CTT | 8 | a0001c0001t0001g0130 a0001c0001t0002g0089 a0001c0001t0002g0183 others(5): Show |
8 | HG01081.hp1 HG02145.hp2 HG02258.hp2 others(5): Show |
intron_variant | MODIFIER | c.683-1907_683-1906d others(4): Show |
MFSD11 | ENSG00000092931.12 | transcript | ENST00000685175.1 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr17 | 76765452 | ||||||
| chr17:76765452 | CT | C | 10 | a0001c0001t0001g0158 a0001c0001t0001g0232 a0001c0001t0001g0233 others(7): Show |
10 | HG00323.hp2 HG01168.hp2 NA18944.hp1 others(7): Show |
intron_variant | MODIFIER | c.683-1906delT | MFSD11 | ENSG00000092931.12 | transcript | ENST00000685175.1 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr17 | 76765452 | ||||||
| chr17:76765452 | CTTT | C | 6 | a0001c0001t0001g0046 a0001c0001t0001g0064 a0001c0001t0001g0069 others(3): Show |
6 | HG02055.hp1 HG02155.hp1 HG02155.hp2 others(3): Show |
intron_variant | MODIFIER | c.683-1908_683-1906d others(5): Show |
MFSD11 | ENSG00000092931.12 | transcript | ENST00000685175.1 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr17 | 76765452 | ||||||
| chr17:76765452 | CTTTT | C | 8 | a0001c0001t0001g0054 a0001c0001t0001g0056 a0001c0001t0001g0057 others(5): Show |
8 | HG00735.hp2 HG02083.hp2 HG02135.hp2 others(5): Show |
intron_variant | MODIFIER | c.683-1909_683-1906d others(6): Show |
MFSD11 | ENSG00000092931.12 | transcript | ENST00000685175.1 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr17 | 76765452 | ||||||
| chr17:76765452 | CTTTTTT | C | 22 | a0001c0001t0001g0129 a0001c0001t0001g0147 a0001c0001t0001g0148 others(19): Show |
23 | HG01243.hp1 HG01884.hp1 HG01891.hp2 others(20): Show |
intron_variant | MODIFIER | c.683-1911_683-1906d others(8): Show |
MFSD11 | ENSG00000092931.12 | transcript | ENST00000685175.1 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr17 | 76765452 | ||||||
| chr17:76765452 | CTTTTTTT | C | 13 | a0001c0001t0001g0128 a0001c0001t0001g0278 a0001c0001t0001g0279 others(10): Show |
13 | HG01106.hp2 HG02109.hp2 HG02145.hp1 others(10): Show |
intron_variant | MODIFIER | c.683-1912_683-1906d others(9): Show |
MFSD11 | ENSG00000092931.12 | transcript | ENST00000685175.1 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr17 | 76765452 | ||||||
| chr17:76765452 | CTTTTTTT others(5): Show |
C | 3 | a0001c0001t0001g0168 a0001c0001t0001g0228 a0001c0001t0001g0235 |
3 | HG00099.hp1 HG00099.hp2 HG01361.hp1 |
intron_variant | MODIFIER | c.683-1917_683-1906d others(14): Show |
MFSD11 | ENSG00000092931.12 | transcript | ENST00000685175.1 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr17 | 76765452 | ||||||
| chr17:76765452 | CTTTTTTT others(10): Show |
C | 3 | a0001c0006t0007g0042 a0001c0006t0007g0043 a0001c0008t0001g0297 |
3 | HG02602.hp1 HG02735.hp1 HG03688.hp1 |
intron_variant | MODIFIER | c.683-1922_683-1906d others(19): Show |
MFSD11 | ENSG00000092931.12 | transcript | ENST00000685175.1 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr17 | 76765452 | ||||||
| chr17:76765511 | G | A | 2 | a0001c0001t0002g0077 a0001c0001t0002g0241 |
2 | NA19060.hp2 NA19065.hp1 |
intron_variant | MODIFIER | c.683-1875G>A | MFSD11 | ENSG00000092931.12 | transcript | ENST00000685175.1 | protein_coding | 8/12 | chr17 | 76765511 | |||||||
| chr17:76765524 | T | G | 2 | a0001c0006t0007g0042 a0001c0006t0007g0043 |
2 | HG02602.hp1 HG02735.hp1 |
intron_variant | MODIFIER | c.683-1862T>G | MFSD11 | ENSG00000092931.12 | transcript | ENST00000685175.1 | protein_coding | 8/12 | chr17 | 76765524 | |||||||
| chr17:76765840 | A | G | 37 | a0001c0001t0001g0105 a0001c0001t0001g0129 a0001c0001t0001g0130 others(34): Show |
38 | HG01069.hp1 HG01099.hp1 HG01243.hp1 others(35): Show |
intron_variant | MODIFIER | c.683-1546A>G | MFSD11 | ENSG00000092931.12 | transcript | ENST00000685175.1 | protein_coding | 8/12 | chr17 | 76765840 | |||||||
| chr17:76765909 | T | C | 3 | a0001c0001t0003g0013 a0001c0001t0003g0019 a0001c0001t0003g0023 |
3 | NA18959.hp2 NA18962.hp2 NA19075.hp2 |
intron_variant | MODIFIER | c.683-1477T>C | MFSD11 | ENSG00000092931.12 | transcript | ENST00000685175.1 | protein_coding | 8/12 | chr17 | 76765909 | |||||||
| chr17:76765947 | C | A | 4 | a0001c0002t0001g0004 a0001c0002t0001g0074 a0001c0002t0001g0075 others(1): Show |
5 | HG01243.hp1 HG01884.hp1 HG02622.hp2 others(2): Show |
intron_variant | MODIFIER | c.683-1439C>A | MFSD11 | ENSG00000092931.12 | transcript | ENST00000685175.1 | protein_coding | 8/12 | chr17 | 76765947 | |||||||
| chr17:76766011 | T | C | 2 | a0001c0006t0007g0042 a0001c0006t0007g0043 |
2 | HG02602.hp1 HG02735.hp1 |
intron_variant | MODIFIER | c.683-1375T>C | MFSD11 | ENSG00000092931.12 | transcript | ENST00000685175.1 | protein_coding | 8/12 | chr17 | 76766011 | |||||||
| chr17:76766098 | T | C | 17 | a0001c0001t0001g0105 a0001c0001t0001g0129 a0001c0001t0001g0130 others(14): Show |
17 | HG01099.hp1 HG01884.hp2 HG01891.hp2 others(14): Show |
intron_variant | MODIFIER | c.683-1288T>C | MFSD11 | ENSG00000092931.12 | transcript | ENST00000685175.1 | protein_coding | 8/12 | chr17 | 76766098 | |||||||
| chr17:76766147 | T | G | 1 | a0001c0001t0001g0179 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.683-1239T>G | MFSD11 | ENSG00000092931.12 | transcript | ENST00000685175.1 | protein_coding | 8/12 | chr17 | 76766147 | |||||||
| chr17:76766418 | C | CA | 39 | a0001c0001t0001g0046 a0001c0001t0001g0047 a0001c0001t0001g0048 others(36): Show |
40 | HG00423.hp2 HG00544.hp1 HG00544.hp2 others(37): Show |
intron_variant | MODIFIER | c.683-950dupA | MFSD11 | ENSG00000092931.12 | transcript | ENST00000685175.1 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr17 | 76766418 | ||||||
| chr17:76766418 | CA | C | 9 | a0001c0001t0001g0136 a0001c0001t0001g0232 a0001c0001t0001g0332 others(6): Show |
9 | HG01069.hp1 HG01168.hp2 HG02965.hp1 others(6): Show |
intron_variant | MODIFIER | c.683-950delA | MFSD11 | ENSG00000092931.12 | transcript | ENST00000685175.1 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr17 | 76766418 | ||||||
| chr17:76766592 | C | T | 1 | a0001c0001t0001g0133 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.683-794C>T | MFSD11 | ENSG00000092931.12 | transcript | ENST00000685175.1 | protein_coding | 8/12 | chr17 | 76766592 | |||||||
| chr17:76766696 | T | C | 62 | a0001c0001t0002g0001 a0001c0001t0002g0008 a0001c0001t0002g0009 others(59): Show |
67 | HG00280.hp2 HG00323.hp1 HG00423.hp1 others(64): Show |
intron_variant | MODIFIER | c.683-690T>C | MFSD11 | ENSG00000092931.12 | transcript | ENST00000685175.1 | protein_coding | 8/12 | chr17 | 76766696 | |||||||
| chr17:76766800 | G | A | 1 | a0001c0001t0001g0056 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.683-586G>A | MFSD11 | ENSG00000092931.12 | transcript | ENST00000685175.1 | protein_coding | 8/12 | chr17 | 76766800 | |||||||
| chr17:76766883 | T | C | 2 | a0001c0006t0007g0042 a0001c0006t0007g0043 |
2 | HG02602.hp1 HG02735.hp1 |
intron_variant | MODIFIER | c.683-503T>C | MFSD11 | ENSG00000092931.12 | transcript | ENST00000685175.1 | protein_coding | 8/12 | chr17 | 76766883 | |||||||
| chr17:76766897 | T | G | 1 | a0001c0001t0002g0203 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.683-489T>G | MFSD11 | ENSG00000092931.12 | transcript | ENST00000685175.1 | protein_coding | 8/12 | chr17 | 76766897 | |||||||
| chr17:76767067 | C | T | 1 | a0001c0001t0002g0111 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.683-319C>T | MFSD11 | ENSG00000092931.12 | transcript | ENST00000685175.1 | protein_coding | 8/12 | chr17 | 76767067 | |||||||
| chr17:76767123 | T | C | 35 | a0001c0001t0001g0105 a0001c0001t0001g0129 a0001c0001t0001g0130 others(32): Show |
36 | HG01069.hp1 HG01099.hp1 HG01243.hp1 others(33): Show |
intron_variant | MODIFIER | c.683-263T>C | MFSD11 | ENSG00000092931.12 | transcript | ENST00000685175.1 | protein_coding | 8/12 | chr17 | 76767123 | |||||||
| chr17:76767518 | C | T | 1 | a0001c0001t0002g0305 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.748+67C>T | MFSD11 | ENSG00000092931.12 | transcript | ENST00000685175.1 | protein_coding | 9/12 | chr17 | 76767518 | |||||||
| chr17:76767640 | T | A | 35 | a0001c0001t0001g0105 a0001c0001t0001g0129 a0001c0001t0001g0130 others(32): Show |
36 | HG01069.hp1 HG01099.hp1 HG01243.hp1 others(33): Show |
intron_variant | MODIFIER | c.748+189T>A | MFSD11 | ENSG00000092931.12 | transcript | ENST00000685175.1 | protein_coding | 9/12 | chr17 | 76767640 | |||||||
| chr17:76767689 | C | A | 34 | a0001c0001t0001g0105 a0001c0001t0001g0129 a0001c0001t0001g0130 others(31): Show |
35 | HG01069.hp1 HG01099.hp1 HG01243.hp1 others(32): Show |
intron_variant | MODIFIER | c.748+238C>A | MFSD11 | ENSG00000092931.12 | transcript | ENST00000685175.1 | protein_coding | 9/12 | chr17 | 76767689 | |||||||
| chr17:76767835 | T | C | 4 | a0001c0002t0001g0004 a0001c0002t0001g0074 a0001c0002t0001g0075 others(1): Show |
5 | HG01243.hp1 HG01884.hp1 HG02622.hp2 others(2): Show |
intron_variant | MODIFIER | c.748+384T>C | MFSD11 | ENSG00000092931.12 | transcript | ENST00000685175.1 | protein_coding | 9/12 | chr17 | 76767835 | |||||||
| chr17:76767844 | C | T | 1 | a0001c0001t0001g0058 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.748+393C>T | MFSD11 | ENSG00000092931.12 | transcript | ENST00000685175.1 | protein_coding | 9/12 | chr17 | 76767844 | |||||||
| chr17:76767896 | C | T | 4 | a0001c0001t0001g0324 a0001c0001t0003g0017 a0001c0001t0003g0018 others(1): Show |
4 | HG01891.hp1 HG02559.hp2 HG02615.hp1 others(1): Show |
intron_variant | MODIFIER | c.748+445C>T | MFSD11 | ENSG00000092931.12 | transcript | ENST00000685175.1 | protein_coding | 9/12 | chr17 | 76767896 | |||||||
| chr17:76768073 | C | T | 35 | a0001c0001t0001g0105 a0001c0001t0001g0129 a0001c0001t0001g0130 others(32): Show |
36 | HG01069.hp1 HG01099.hp1 HG01243.hp1 others(33): Show |
intron_variant | MODIFIER | c.748+622C>T | MFSD11 | ENSG00000092931.12 | transcript | ENST00000685175.1 | protein_coding | 9/12 | chr17 | 76768073 | |||||||
| chr17:76768305 | C | CA | 13 | a0001c0001t0001g0217 a0001c0001t0001g0227 a0001c0001t0001g0260 others(10): Show |
13 | HG00733.hp1 HG02027.hp2 HG02056.hp2 others(10): Show |
intron_variant | MODIFIER | c.748+873dupA | MFSD11 | ENSG00000092931.12 | transcript | ENST00000685175.1 | protein_coding | 9/12 | INFO_REALIGN_3_PRIME | chr17 | 76768305 | ||||||
| chr17:76768305 | CA | C | 7 | a0001c0001t0001g0072 a0001c0001t0001g0136 a0001c0001t0001g0175 others(4): Show |
7 | HG01099.hp2 HG02155.hp1 HG02155.hp2 others(4): Show |
intron_variant | MODIFIER | c.748+873delA | MFSD11 | ENSG00000092931.12 | transcript | ENST00000685175.1 | protein_coding | 9/12 | INFO_REALIGN_3_PRIME | chr17 | 76768305 | ||||||
| chr17:76768414 | T | C | 2 | a0001c0006t0007g0042 a0001c0006t0007g0043 |
2 | HG02602.hp1 HG02735.hp1 |
intron_variant | MODIFIER | c.748+963T>C | MFSD11 | ENSG00000092931.12 | transcript | ENST00000685175.1 | protein_coding | 9/12 | chr17 | 76768414 | |||||||
| chr17:76768465 | C | T | 6 | a0001c0001t0001g0105 a0001c0001t0001g0130 a0001c0001t0006g0325 others(3): Show |
6 | HG01099.hp1 HG01884.hp2 HG02145.hp2 others(3): Show |
intron_variant | MODIFIER | c.748+1014C>T | MFSD11 | ENSG00000092931.12 | transcript | ENST00000685175.1 | protein_coding | 9/12 | chr17 | 76768465 | |||||||
| chr17:76768497 | A | T | 33 | a0001c0001t0001g0105 a0001c0001t0001g0129 a0001c0001t0001g0130 others(30): Show |
34 | HG01069.hp1 HG01099.hp1 HG01243.hp1 others(31): Show |
intron_variant | MODIFIER | c.748+1046A>T | MFSD11 | ENSG00000092931.12 | transcript | ENST00000685175.1 | protein_coding | 9/12 | chr17 | 76768497 | |||||||
| chr17:76768702 | G | T | 1 | a0001c0001t0001g0335 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.749-1044G>T | MFSD11 | ENSG00000092931.12 | transcript | ENST00000685175.1 | protein_coding | 9/12 | chr17 | 76768702 | |||||||
| chr17:76768733 | C | T | 11 | a0001c0001t0001g0129 a0001c0001t0001g0147 a0001c0001t0001g0148 others(8): Show |
11 | HG01891.hp2 HG02622.hp1 HG02818.hp1 others(8): Show |
intron_variant | MODIFIER | c.749-1013C>T | MFSD11 | ENSG00000092931.12 | transcript | ENST00000685175.1 | protein_coding | 9/12 | chr17 | 76768733 | |||||||
| chr17:76768793 | T | A | 2 | a0001c0004t0001g0100 a0001c0004t0001g0131 |
2 | NA18522.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.749-953T>A | MFSD11 | ENSG00000092931.12 | transcript | ENST00000685175.1 | protein_coding | 9/12 | chr17 | 76768793 | |||||||
| chr17:76768814 | G | A | 9 | a0001c0001t0005g0035 a0001c0001t0005g0036 a0001c0001t0005g0037 others(6): Show |
10 | HG01243.hp1 HG01884.hp1 HG02622.hp2 others(7): Show |
intron_variant | MODIFIER | c.749-932G>A | MFSD11 | ENSG00000092931.12 | transcript | ENST00000685175.1 | protein_coding | 9/12 | chr17 | 76768814 | |||||||
| chr17:76768857 | T | C | 2 | a0001c0006t0007g0042 a0001c0006t0007g0043 |
2 | HG02602.hp1 HG02735.hp1 |
intron_variant | MODIFIER | c.749-889T>C | MFSD11 | ENSG00000092931.12 | transcript | ENST00000685175.1 | protein_coding | 9/12 | chr17 | 76768857 | |||||||
| chr17:76768943 | G | A | 6 | a0001c0001t0001g0105 a0001c0001t0001g0130 a0001c0001t0006g0325 others(3): Show |
6 | HG01099.hp1 HG01884.hp2 HG02145.hp2 others(3): Show |
intron_variant | MODIFIER | c.749-803G>A | MFSD11 | ENSG00000092931.12 | transcript | ENST00000685175.1 | protein_coding | 9/12 | chr17 | 76768943 | |||||||
| chr17:76768985 | C | CA | 9 | a0001c0001t0001g0010 a0001c0001t0001g0099 a0001c0001t0001g0261 others(6): Show |
10 | HG02273.hp1 HG02293.hp2 HG02717.hp2 others(7): Show |
intron_variant | MODIFIER | c.749-743dupA | MFSD11 | ENSG00000092931.12 | transcript | ENST00000685175.1 | protein_coding | 9/12 | INFO_REALIGN_3_PRIME | chr17 | 76768985 | ||||||
| chr17:76768985 | CA | C | 29 | a0001c0001t0001g0048 a0001c0001t0001g0105 a0001c0001t0001g0117 others(26): Show |
30 | HG00423.hp2 HG00544.hp1 HG00544.hp2 others(27): Show |
intron_variant | MODIFIER | c.749-743delA | MFSD11 | ENSG00000092931.12 | transcript | ENST00000685175.1 | protein_coding | 9/12 | INFO_REALIGN_3_PRIME | chr17 | 76768985 | ||||||
| chr17:76768999 | A | C | 3 | a0001c0001t0005g0037 a0001c0001t0005g0038 a0001c0001t0005g0039 |
3 | HG02630.hp1 HG03209.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.749-747A>C | MFSD11 | ENSG00000092931.12 | transcript | ENST00000685175.1 | protein_coding | 9/12 | chr17 | 76768999 | |||||||
| chr17:76769178 | T | C | 4 | a0001c0001t0001g0290 a0001c0001t0001g0291 a0001c0001t0001g0292 others(1): Show |
4 | HG02572.hp2 HG02809.hp1 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.749-568T>C | MFSD11 | ENSG00000092931.12 | transcript | ENST00000685175.1 | protein_coding | 9/12 | chr17 | 76769178 | |||||||
| chr17:76769368 | C | T | 11 | a0001c0001t0001g0129 a0001c0001t0001g0147 a0001c0001t0001g0148 others(8): Show |
11 | HG01891.hp2 HG02622.hp1 HG02818.hp1 others(8): Show |
intron_variant | MODIFIER | c.749-378C>T | MFSD11 | ENSG00000092931.12 | transcript | ENST00000685175.1 | protein_coding | 9/12 | chr17 | 76769368 | |||||||
| chr17:76769469 | TC | T | 61 | a0001c0001t0002g0001 a0001c0001t0002g0008 a0001c0001t0002g0009 others(58): Show |
66 | HG00280.hp2 HG00323.hp1 HG00423.hp1 others(63): Show |
intron_variant | MODIFIER | c.749-275delC | MFSD11 | ENSG00000092931.12 | transcript | ENST00000685175.1 | protein_coding | 9/12 | INFO_REALIGN_3_PRIME | chr17 | 76769469 | ||||||
| chr17:76769493 | C | T | 5 | a0001c0001t0001g0134 a0001c0001t0001g0138 a0001c0001t0001g0139 others(2): Show |
5 | HG02273.hp2 NA18612.hp1 NA18962.hp1 others(2): Show |
intron_variant | MODIFIER | c.749-253C>T | MFSD11 | ENSG00000092931.12 | transcript | ENST00000685175.1 | protein_coding | 9/12 | chr17 | 76769493 | |||||||
| chr17:76769537 | G | A | 6 | a0001c0001t0001g0324 a0001c0001t0003g0011 a0001c0001t0003g0014 others(3): Show |
6 | HG01891.hp1 HG02258.hp1 HG02486.hp2 others(3): Show |
intron_variant | MODIFIER | c.749-209G>A | MFSD11 | ENSG00000092931.12 | transcript | ENST00000685175.1 | protein_coding | 9/12 | chr17 | 76769537 | |||||||
| chr17:76769542 | C | T | 1 | a0004c0010t0001g0169 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.749-204C>T | MFSD11 | ENSG00000092931.12 | transcript | ENST00000685175.1 | protein_coding | 9/12 | chr17 | 76769542 | |||||||
| chr17:76769642 | T | C | 5 | a0001c0001t0005g0035 a0001c0001t0005g0036 a0001c0001t0005g0037 others(2): Show |
5 | HG02630.hp1 HG02886.hp2 HG03209.hp1 others(2): Show |
intron_variant | MODIFIER | c.749-104T>C | MFSD11 | ENSG00000092931.12 | transcript | ENST00000685175.1 | protein_coding | 9/12 | chr17 | 76769642 | |||||||
| chr17:76769655 | G | A | 6 | a0001c0001t0001g0105 a0001c0001t0001g0130 a0001c0001t0006g0325 others(3): Show |
6 | HG01099.hp1 HG01884.hp2 HG02145.hp2 others(3): Show |
intron_variant | MODIFIER | c.749-91G>A | MFSD11 | ENSG00000092931.12 | transcript | ENST00000685175.1 | protein_coding | 9/12 | chr17 | 76769655 | |||||||
| chr17:76769916 | T | C | 3 | a0001c0001t0001g0174 a0001c0001t0001g0175 a0001c0001t0001g0256 |
3 | HG00642.hp1 HG01099.hp2 HG01192.hp2 |
intron_variant | MODIFIER | c.874+45T>C | MFSD11 | ENSG00000092931.12 | transcript | ENST00000685175.1 | protein_coding | 10/12 | chr17 | 76769916 | |||||||
| chr17:76770031 | C | CT | 37 | a0001c0001t0001g0105 a0001c0001t0001g0129 a0001c0001t0001g0130 others(34): Show |
37 | HG00735.hp2 HG01069.hp1 HG01099.hp1 others(34): Show |
intron_variant | MODIFIER | c.874+177dupT | MFSD11 | ENSG00000092931.12 | transcript | ENST00000685175.1 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr17 | 76770031 | ||||||
| chr17:76770031 | C | CTT | 8 | a0001c0001t0001g0279 a0001c0001t0003g0022 a0001c0001t0003g0028 others(5): Show |
8 | HG02257.hp2 HG02572.hp1 HG02630.hp1 others(5): Show |
intron_variant | MODIFIER | c.874+176_874+177dup others(2): Show |
MFSD11 | ENSG00000092931.12 | transcript | ENST00000685175.1 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr17 | 76770031 | ||||||
| chr17:76770047 | T | C | 1 | a0001c0001t0001g0263 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.874+176T>C | MFSD11 | ENSG00000092931.12 | transcript | ENST00000685175.1 | protein_coding | 10/12 | chr17 | 76770047 | |||||||
| chr17:76770054 | CAG | C | 60 | a0001c0001t0002g0001 a0001c0001t0002g0008 a0001c0001t0002g0009 others(57): Show |
65 | HG00280.hp2 HG00323.hp1 HG00423.hp1 others(62): Show |
intron_variant | MODIFIER | c.874+186_874+187del others(2): Show |
MFSD11 | ENSG00000092931.12 | transcript | ENST00000685175.1 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr17 | 76770054 | ||||||
| chr17:76770062 | C | T | 1 | a0001c0001t0003g0021 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.874+191C>T | MFSD11 | ENSG00000092931.12 | transcript | ENST00000685175.1 | protein_coding | 10/12 | chr17 | 76770062 | |||||||
| chr17:76770089 | G | A | 2 | a0001c0001t0002g0113 a0001c0001t0002g0119 |
2 | HG00609.hp1 NA18998.hp1 |
intron_variant | MODIFIER | c.874+218G>A | MFSD11 | ENSG00000092931.12 | transcript | ENST00000685175.1 | protein_coding | 10/12 | chr17 | 76770089 | |||||||
| chr17:76770138 | C | T | 2 | a0001c0006t0007g0042 a0001c0006t0007g0043 |
2 | HG02602.hp1 HG02735.hp1 |
intron_variant | MODIFIER | c.874+267C>T | MFSD11 | ENSG00000092931.12 | transcript | ENST00000685175.1 | protein_coding | 10/12 | chr17 | 76770138 | |||||||
| chr17:76770392 | A | G | 2 | a0001c0006t0007g0042 a0001c0006t0007g0043 |
2 | HG02602.hp1 HG02735.hp1 |
intron_variant | MODIFIER | c.874+521A>G | MFSD11 | ENSG00000092931.12 | transcript | ENST00000685175.1 | protein_coding | 10/12 | chr17 | 76770392 | |||||||
| chr17:76770568 | G | A | 1 | a0001c0001t0001g0153 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.874+697G>A | MFSD11 | ENSG00000092931.12 | transcript | ENST00000685175.1 | protein_coding | 10/12 | chr17 | 76770568 | |||||||
| chr17:76770727 | TC | T | 5 | a0001c0001t0001g0278 a0001c0001t0001g0281 a0001c0001t0001g0282 others(2): Show |
5 | HG02145.hp1 HG02896.hp1 HG02976.hp2 others(2): Show |
intron_variant | MODIFIER | c.874+858delC | MFSD11 | ENSG00000092931.12 | transcript | ENST00000685175.1 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr17 | 76770727 | ||||||
| chr17:76770926 | T | C | 1 | a0001c0001t0001g0154 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.874+1055T>C | MFSD11 | ENSG00000092931.12 | transcript | ENST00000685175.1 | protein_coding | 10/12 | chr17 | 76770926 | |||||||
| chr17:76771220 | C | G | 1 | a0001c0001t0001g0311 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.874+1349C>G | MFSD11 | ENSG00000092931.12 | transcript | ENST00000685175.1 | protein_coding | 10/12 | chr17 | 76771220 | |||||||
| chr17:76771237 | G | A | 4 | a0001c0001t0003g0025 a0001c0001t0003g0026 a0001c0001t0003g0027 others(1): Show |
4 | HG01106.hp2 HG02109.hp2 HG02572.hp1 others(1): Show |
intron_variant | MODIFIER | c.874+1366G>A | MFSD11 | ENSG00000092931.12 | transcript | ENST00000685175.1 | protein_coding | 10/12 | chr17 | 76771237 | |||||||
| chr17:76771332 | G | T | 2 | a0001c0006t0007g0042 a0001c0006t0007g0043 |
2 | HG02602.hp1 HG02735.hp1 |
intron_variant | MODIFIER | c.874+1461G>T | MFSD11 | ENSG00000092931.12 | transcript | ENST00000685175.1 | protein_coding | 10/12 | chr17 | 76771332 | |||||||
| chr17:76771418 | T | C | 4 | a0001c0001t0003g0025 a0001c0001t0003g0026 a0001c0001t0003g0027 others(1): Show |
4 | HG01106.hp2 HG02109.hp2 HG02572.hp1 others(1): Show |
intron_variant | MODIFIER | c.874+1547T>C | MFSD11 | ENSG00000092931.12 | transcript | ENST00000685175.1 | protein_coding | 10/12 | chr17 | 76771418 | |||||||
| chr17:76771486 | A | C | 1 | a0001c0001t0001g0310 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.874+1615A>C | MFSD11 | ENSG00000092931.12 | transcript | ENST00000685175.1 | protein_coding | 10/12 | chr17 | 76771486 | |||||||
| chr17:76771493 | T | A | 1 | a0001c0001t0001g0310 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.874+1622T>A | MFSD11 | ENSG00000092931.12 | transcript | ENST00000685175.1 | protein_coding | 10/12 | chr17 | 76771493 | |||||||
| chr17:76771494 | G | A | 1 | a0001c0001t0001g0310 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.874+1623G>A | MFSD11 | ENSG00000092931.12 | transcript | ENST00000685175.1 | protein_coding | 10/12 | chr17 | 76771494 | |||||||
| chr17:76771497 | C | T | 1 | a0001c0001t0001g0310 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.874+1626C>T | MFSD11 | ENSG00000092931.12 | transcript | ENST00000685175.1 | protein_coding | 10/12 | chr17 | 76771497 | |||||||
| chr17:76771498 | A | T | 1 | a0001c0001t0001g0310 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.874+1627A>T | MFSD11 | ENSG00000092931.12 | transcript | ENST00000685175.1 | protein_coding | 10/12 | chr17 | 76771498 | |||||||
| chr17:76771500 | A | G | 1 | a0001c0001t0001g0310 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.874+1629A>G | MFSD11 | ENSG00000092931.12 | transcript | ENST00000685175.1 | protein_coding | 10/12 | chr17 | 76771500 | |||||||
| chr17:76771502 | A | T | 1 | a0001c0001t0001g0310 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.874+1631A>T | MFSD11 | ENSG00000092931.12 | transcript | ENST00000685175.1 | protein_coding | 10/12 | chr17 | 76771502 | |||||||
| chr17:76771505 | G | C | 1 | a0001c0001t0001g0310 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.874+1634G>C | MFSD11 | ENSG00000092931.12 | transcript | ENST00000685175.1 | protein_coding | 10/12 | chr17 | 76771505 | |||||||
| chr17:76771508 | T | C | 1 | a0001c0001t0001g0310 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.874+1637T>C | MFSD11 | ENSG00000092931.12 | transcript | ENST00000685175.1 | protein_coding | 10/12 | chr17 | 76771508 | |||||||
| chr17:76771523 | G | C | 1 | a0001c0001t0001g0310 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.874+1652G>C | MFSD11 | ENSG00000092931.12 | transcript | ENST00000685175.1 | protein_coding | 10/12 | chr17 | 76771523 | |||||||
| chr17:76771525 | A | C | 1 | a0001c0001t0001g0310 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.874+1654A>C | MFSD11 | ENSG00000092931.12 | transcript | ENST00000685175.1 | protein_coding | 10/12 | chr17 | 76771525 | |||||||
| chr17:76771526 | T | A | 1 | a0001c0001t0001g0310 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.874+1655T>A | MFSD11 | ENSG00000092931.12 | transcript | ENST00000685175.1 | protein_coding | 10/12 | chr17 | 76771526 | |||||||
| chr17:76771528 | C | T | 1 | a0001c0001t0001g0310 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.874+1657C>T | MFSD11 | ENSG00000092931.12 | transcript | ENST00000685175.1 | protein_coding | 10/12 | chr17 | 76771528 | |||||||
| chr17:76771530 | G | T | 1 | a0001c0001t0001g0310 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.874+1659G>T | MFSD11 | ENSG00000092931.12 | transcript | ENST00000685175.1 | protein_coding | 10/12 | chr17 | 76771530 | |||||||
| chr17:76771531 | A | T | 1 | a0001c0001t0001g0310 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.874+1660A>T | MFSD11 | ENSG00000092931.12 | transcript | ENST00000685175.1 | protein_coding | 10/12 | chr17 | 76771531 | |||||||
| chr17:76771539 | A | T | 1 | a0001c0001t0001g0310 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.874+1668A>T | MFSD11 | ENSG00000092931.12 | transcript | ENST00000685175.1 | protein_coding | 10/12 | chr17 | 76771539 | |||||||
| chr17:76771542 | A | T | 1 | a0001c0001t0001g0310 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.874+1671A>T | MFSD11 | ENSG00000092931.12 | transcript | ENST00000685175.1 | protein_coding | 10/12 | chr17 | 76771542 | |||||||
| chr17:76771546 | A | G | 1 | a0001c0001t0001g0310 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.874+1675A>G | MFSD11 | ENSG00000092931.12 | transcript | ENST00000685175.1 | protein_coding | 10/12 | chr17 | 76771546 | |||||||
| chr17:76771548 | C | G | 1 | a0001c0001t0001g0310 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.874+1677C>G | MFSD11 | ENSG00000092931.12 | transcript | ENST00000685175.1 | protein_coding | 10/12 | chr17 | 76771548 | |||||||
| chr17:76771549 | T | C | 1 | a0001c0001t0001g0310 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.874+1678T>C | MFSD11 | ENSG00000092931.12 | transcript | ENST00000685175.1 | protein_coding | 10/12 | chr17 | 76771549 | |||||||
| chr17:76771553 | T | A | 1 | a0001c0001t0001g0310 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.874+1682T>A | MFSD11 | ENSG00000092931.12 | transcript | ENST00000685175.1 | protein_coding | 10/12 | chr17 | 76771553 | |||||||
| chr17:76771557 | T | C | 1 | a0001c0001t0001g0310 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.874+1686T>C | MFSD11 | ENSG00000092931.12 | transcript | ENST00000685175.1 | protein_coding | 10/12 | chr17 | 76771557 | |||||||
| chr17:76771558 | C | A | 1 | a0001c0001t0001g0310 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.874+1687C>A | MFSD11 | ENSG00000092931.12 | transcript | ENST00000685175.1 | protein_coding | 10/12 | chr17 | 76771558 | |||||||
| chr17:76771668 | G | A | 1 | a0001c0001t0001g0227 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.874+1797G>A | MFSD11 | ENSG00000092931.12 | transcript | ENST00000685175.1 | protein_coding | 10/12 | chr17 | 76771668 | |||||||
| chr17:76771802 | C | T | 32 | a0001c0001t0001g0105 a0001c0001t0001g0129 a0001c0001t0001g0130 others(29): Show |
33 | HG01069.hp1 HG01099.hp1 HG01243.hp1 others(30): Show |
intron_variant | MODIFIER | c.874+1931C>T | MFSD11 | ENSG00000092931.12 | transcript | ENST00000685175.1 | protein_coding | 10/12 | chr17 | 76771802 | |||||||
| chr17:76772032 | G | C | 4 | a0001c0001t0001g0010 a0001c0001t0001g0099 a0001c0001t0001g0272 others(1): Show |
5 | HG02717.hp2 HG02818.hp2 HG02895.hp1 others(2): Show |
intron_variant | MODIFIER | c.874+2161G>C | MFSD11 | ENSG00000092931.12 | transcript | ENST00000685175.1 | protein_coding | 10/12 | chr17 | 76772032 | |||||||
| chr17:76772057 | T | C | 2 | a0001c0006t0007g0042 a0001c0006t0007g0043 |
2 | HG02602.hp1 HG02735.hp1 |
intron_variant | MODIFIER | c.874+2186T>C | MFSD11 | ENSG00000092931.12 | transcript | ENST00000685175.1 | protein_coding | 10/12 | chr17 | 76772057 | |||||||
| chr17:76772158 | C | G | 11 | a0001c0001t0001g0129 a0001c0001t0001g0147 a0001c0001t0001g0148 others(8): Show |
11 | HG01891.hp2 HG02622.hp1 HG02818.hp1 others(8): Show |
intron_variant | MODIFIER | c.874+2287C>G | MFSD11 | ENSG00000092931.12 | transcript | ENST00000685175.1 | protein_coding | 10/12 | chr17 | 76772158 | |||||||
| chr17:76772294 | G | A | 1 | a0001c0001t0003g0041 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.874+2423G>A | MFSD11 | ENSG00000092931.12 | transcript | ENST00000685175.1 | protein_coding | 10/12 | chr17 | 76772294 | |||||||
| chr17:76772417 | A | C | 1 | a0001c0005t0012g0195 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.874+2546A>C | MFSD11 | ENSG00000092931.12 | transcript | ENST00000685175.1 | protein_coding | 10/12 | chr17 | 76772417 | |||||||
| chr17:76772514 | CT | C | 32 | a0001c0001t0001g0129 a0001c0001t0001g0130 a0001c0001t0001g0147 others(29): Show |
33 | HG01099.hp1 HG01168.hp2 HG01243.hp1 others(30): Show |
intron_variant | MODIFIER | c.875-2463delT | MFSD11 | ENSG00000092931.12 | transcript | ENST00000685175.1 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr17 | 76772514 | ||||||
| chr17:76772514 | CTT | C | 10 | a0001c0001t0001g0105 a0001c0001t0004g0012 a0001c0001t0004g0030 others(7): Show |
10 | HG01069.hp1 HG02258.hp2 HG02602.hp1 others(7): Show |
intron_variant | MODIFIER | c.875-2464_875-2463d others(4): Show |
MFSD11 | ENSG00000092931.12 | transcript | ENST00000685175.1 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr17 | 76772514 | ||||||
| chr17:76772532 | T | C | 7 | a0001c0001t0001g0101 a0001c0001t0001g0117 a0001c0001t0001g0133 others(4): Show |
7 | HG02040.hp1 HG02074.hp1 NA18991.hp1 others(4): Show |
intron_variant | MODIFIER | c.875-2465T>C | MFSD11 | ENSG00000092931.12 | transcript | ENST00000685175.1 | protein_coding | 10/12 | chr17 | 76772532 | |||||||
| chr17:76772666 | C | T | 1 | a0001c0001t0002g0181 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.875-2331C>T | MFSD11 | ENSG00000092931.12 | transcript | ENST00000685175.1 | protein_coding | 10/12 | chr17 | 76772666 | |||||||
| chr17:76772676 | C | T | 1 | a0001c0001t0001g0150 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.875-2321C>T | MFSD11 | ENSG00000092931.12 | transcript | ENST00000685175.1 | protein_coding | 10/12 | chr17 | 76772676 | |||||||
| chr17:76772728 | G | A | 6 | a0001c0001t0001g0105 a0001c0001t0001g0130 a0001c0001t0006g0325 others(3): Show |
6 | HG01099.hp1 HG01884.hp2 HG02145.hp2 others(3): Show |
intron_variant | MODIFIER | c.875-2269G>A | MFSD11 | ENSG00000092931.12 | transcript | ENST00000685175.1 | protein_coding | 10/12 | chr17 | 76772728 | |||||||
| chr17:76773074 | C | T | 1 | a0001c0005t0012g0195 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.875-1923C>T | MFSD11 | ENSG00000092931.12 | transcript | ENST00000685175.1 | protein_coding | 10/12 | chr17 | 76773074 | |||||||
| chr17:76773402 | G | A | 35 | a0001c0001t0001g0105 a0001c0001t0001g0129 a0001c0001t0001g0130 others(32): Show |
36 | HG01069.hp1 HG01099.hp1 HG01243.hp1 others(33): Show |
intron_variant | MODIFIER | c.875-1595G>A | MFSD11 | ENSG00000092931.12 | transcript | ENST00000685175.1 | protein_coding | 10/12 | chr17 | 76773402 | |||||||
| chr17:76773479 | T | G | 16 | a0001c0001t0001g0097 a0001c0001t0001g0129 a0001c0001t0001g0147 others(13): Show |
16 | HG01069.hp2 HG01071.hp2 HG01891.hp2 others(13): Show |
intron_variant | MODIFIER | c.875-1518T>G | MFSD11 | ENSG00000092931.12 | transcript | ENST00000685175.1 | protein_coding | 10/12 | chr17 | 76773479 | |||||||
| chr17:76773521 | T | C | 5 | a0001c0001t0002g0202 a0001c0001t0002g0204 a0001c0001t0002g0206 others(2): Show |
5 | HG02056.hp2 HG02132.hp2 HG04228.hp2 others(2): Show |
intron_variant | MODIFIER | c.875-1476T>C | MFSD11 | ENSG00000092931.12 | transcript | ENST00000685175.1 | protein_coding | 10/12 | chr17 | 76773521 | |||||||
| chr17:76773796 | C | G | 1 | a0001c0001t0010g0090 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.875-1201C>G | MFSD11 | ENSG00000092931.12 | transcript | ENST00000685175.1 | protein_coding | 10/12 | chr17 | 76773796 | |||||||
| chr17:76773956 | T | C | 2 | a0001c0006t0007g0042 a0001c0006t0007g0043 |
2 | HG02602.hp1 HG02735.hp1 |
intron_variant | MODIFIER | c.875-1041T>C | MFSD11 | ENSG00000092931.12 | transcript | ENST00000685175.1 | protein_coding | 10/12 | chr17 | 76773956 | |||||||
| chr17:76774072 | T | C | 1 | a0001c0001t0013g0132 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.875-925T>C | MFSD11 | ENSG00000092931.12 | transcript | ENST00000685175.1 | protein_coding | 10/12 | chr17 | 76774072 | |||||||
| chr17:76774136 | G | A | 2 | a0001c0006t0007g0042 a0001c0006t0007g0043 |
2 | HG02602.hp1 HG02735.hp1 |
intron_variant | MODIFIER | c.875-861G>A | MFSD11 | ENSG00000092931.12 | transcript | ENST00000685175.1 | protein_coding | 10/12 | chr17 | 76774136 | |||||||
| chr17:76774140 | G | A | 1 | a0001c0001t0001g0261 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.875-857G>A | MFSD11 | ENSG00000092931.12 | transcript | ENST00000685175.1 | protein_coding | 10/12 | chr17 | 76774140 | |||||||
| chr17:76774181 | C | T | 3 | a0001c0001t0003g0017 a0001c0001t0003g0018 a0001c0001t0003g0040 |
3 | HG01891.hp1 HG02559.hp2 HG02615.hp1 |
intron_variant | MODIFIER | c.875-816C>T | MFSD11 | ENSG00000092931.12 | transcript | ENST00000685175.1 | protein_coding | 10/12 | chr17 | 76774181 | |||||||
| chr17:76774281 | G | A | 2 | a0001c0001t0001g0069 a0001c0001t0006g0325 |
2 | HG01884.hp2 HG02055.hp1 |
intron_variant | MODIFIER | c.875-716G>A | MFSD11 | ENSG00000092931.12 | transcript | ENST00000685175.1 | protein_coding | 10/12 | chr17 | 76774281 | |||||||
| chr17:76774401 | T | G | 1 | a0001c0001t0002g0110 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.875-596T>G | MFSD11 | ENSG00000092931.12 | transcript | ENST00000685175.1 | protein_coding | 10/12 | chr17 | 76774401 | |||||||
| chr17:76774740 | G | C | 3 | a0001c0001t0002g0187 a0001c0001t0002g0305 a0001c0001t0002g0315 |
3 | HG00558.hp2 NA18972.hp2 NA19062.hp1 |
intron_variant | MODIFIER | c.875-257G>C | MFSD11 | ENSG00000092931.12 | transcript | ENST00000685175.1 | protein_coding | 10/12 | chr17 | 76774740 | |||||||
| chr17:76774741 | G | T | 2 | a0001c0001t0001g0279 a0002c0007t0001g0280 |
2 | HG02257.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.875-256G>T | MFSD11 | ENSG00000092931.12 | transcript | ENST00000685175.1 | protein_coding | 10/12 | chr17 | 76774741 | |||||||
| chr17:76774917 | T | G | 1 | a0001c0005t0012g0195 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.875-80T>G | MFSD11 | ENSG00000092931.12 | transcript | ENST00000685175.1 | protein_coding | 10/12 | chr17 | 76774917 | |||||||
| chr17:76774959 | G | A | 3 | a0001c0001t0001g0328 a0001c0001t0001g0329 a0001c0001t0001g0333 |
3 | HG03098.hp2 HG03209.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.875-38G>A | MFSD11 | ENSG00000092931.12 | transcript | ENST00000685175.1 | protein_coding | 10/12 | chr17 | 76774959 | |||||||
| chr17:76775217 | G | A | 6 | a0001c0001t0004g0012 a0001c0001t0004g0030 a0001c0001t0004g0031 others(3): Show |
6 | HG01069.hp1 HG02258.hp2 HG02630.hp2 others(3): Show |
intron_variant | MODIFIER | c.1049+46G>A | MFSD11 | ENSG00000092931.12 | transcript | ENST00000685175.1 | protein_coding | 11/12 | chr17 | 76775217 | |||||||
| chr17:76775506 | G | C | 1 | a0001c0001t0001g0057 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.1049+335G>C | MFSD11 | ENSG00000092931.12 | transcript | ENST00000685175.1 | protein_coding | 11/12 | chr17 | 76775506 | |||||||
| chr17:76775506 | G | T | 2 | a0001c0001t0001g0306 a0001c0001t0001g0307 |
2 | NA18965.hp2 NA18971.hp2 |
intron_variant | MODIFIER | c.1049+335G>T | MFSD11 | ENSG00000092931.12 | transcript | ENST00000685175.1 | protein_coding | 11/12 | chr17 | 76775506 | |||||||
| chr17:76775679 | T | C | 1 | a0001c0001t0001g0044 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.1049+508T>C | MFSD11 | ENSG00000092931.12 | transcript | ENST00000685175.1 | protein_coding | 11/12 | chr17 | 76775679 | |||||||
| chr17:76775682 | A | G | 6 | a0001c0001t0004g0012 a0001c0001t0004g0030 a0001c0001t0004g0031 others(3): Show |
6 | HG01069.hp1 HG02258.hp2 HG02630.hp2 others(3): Show |
intron_variant | MODIFIER | c.1049+511A>G | MFSD11 | ENSG00000092931.12 | transcript | ENST00000685175.1 | protein_coding | 11/12 | chr17 | 76775682 | |||||||
| chr17:76775742 | T | A | 4 | a0001c0002t0001g0004 a0001c0002t0001g0074 a0001c0002t0001g0075 others(1): Show |
5 | HG01243.hp1 HG01884.hp1 HG02622.hp2 others(2): Show |
intron_variant | MODIFIER | c.1049+571T>A | MFSD11 | ENSG00000092931.12 | transcript | ENST00000685175.1 | protein_coding | 11/12 | chr17 | 76775742 | |||||||
| chr17:76776043 | A | G | 1 | a0001c0001t0001g0162 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.1050-363A>G | MFSD11 | ENSG00000092931.12 | transcript | ENST00000685175.1 | protein_coding | 11/12 | chr17 | 76776043 | |||||||
| chr17:76776336 | G | A | 1 | a0001c0001t0013g0132 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.1050-70G>A | MFSD11 | ENSG00000092931.12 | transcript | ENST00000685175.1 | protein_coding | 11/12 | chr17 | 76776336 | |||||||
| chr17:76776715 | G | A | 22 | a0001c0001t0001g0105 a0001c0001t0001g0130 a0001c0001t0004g0012 others(19): Show |
23 | HG01069.hp1 HG01099.hp1 HG01243.hp1 others(20): Show |
intron_variant | MODIFIER | c.1185+174G>A | MFSD11 | ENSG00000092931.12 | transcript | ENST00000685175.1 | protein_coding | 12/12 | chr17 | 76776715 | |||||||
| chr17:76776815 | AT | A | 24 | a0001c0001t0001g0105 a0001c0001t0001g0130 a0001c0001t0004g0012 others(21): Show |
25 | HG01069.hp1 HG01099.hp1 HG01243.hp1 others(22): Show |
intron_variant | MODIFIER | c.1185+284delT | MFSD11 | ENSG00000092931.12 | transcript | ENST00000685175.1 | protein_coding | 12/12 | INFO_REALIGN_3_PRIME | chr17 | 76776815 | ||||||
| chr17:76776844 | G | T | 1 | a0001c0005t0012g0195 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.1185+303G>T | MFSD11 | ENSG00000092931.12 | transcript | ENST00000685175.1 | protein_coding | 12/12 | chr17 | 76776844 | |||||||
| chr17:76776853 | C | T | 2 | a0001c0001t0001g0226 a0001c0001t0001g0318 |
2 | HG00735.hp1 HG01106.hp1 |
intron_variant | MODIFIER | c.1185+312C>T | MFSD11 | ENSG00000092931.12 | transcript | ENST00000685175.1 | protein_coding | 12/12 | chr17 | 76776853 | |||||||
| chr17:76776942 | C | T | 1 | a0001c0001t0001g0188 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.1185+401C>T | MFSD11 | ENSG00000092931.12 | transcript | ENST00000685175.1 | protein_coding | 12/12 | chr17 | 76776942 | |||||||
| chr17:76776994 | G | A | 2 | a0001c0006t0007g0042 a0001c0006t0007g0043 |
2 | HG02602.hp1 HG02735.hp1 |
intron_variant | MODIFIER | c.1185+453G>A | MFSD11 | ENSG00000092931.12 | transcript | ENST00000685175.1 | protein_coding | 12/12 | chr17 | 76776994 | |||||||
| chr17:76776996 | C | T | 1 | a0001c0001t0013g0132 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.1185+455C>T | MFSD11 | ENSG00000092931.12 | transcript | ENST00000685175.1 | protein_coding | 12/12 | chr17 | 76776996 | |||||||
| chr17:76777064 | G | GAGACCAT others(7): Show |
1 | a0001c0005t0012g0195 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.1185+525_1185+538d others(16): Show |
MFSD11 | ENSG00000092931.12 | transcript | ENST00000685175.1 | protein_coding | 12/12 | INFO_REALIGN_3_PRIME | chr17 | 76777064 | ||||||
| chr17:76777129 | G | A | 1 | a0001c0001t0005g0037 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.1185+588G>A | MFSD11 | ENSG00000092931.12 | transcript | ENST00000685175.1 | protein_coding | 12/12 | chr17 | 76777129 | |||||||
| chr17:76777200 | G | A | 2 | a0001c0001t0001g0287 a0001c0001t0001g0293 |
2 | HG03041.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.1185+659G>A | MFSD11 | ENSG00000092931.12 | transcript | ENST00000685175.1 | protein_coding | 12/12 | chr17 | 76777200 | |||||||
| chr17:76777267 | C | CA | 12 | a0001c0001t0001g0046 a0001c0001t0001g0064 a0001c0001t0001g0068 others(9): Show |
12 | HG00741.hp2 HG02055.hp2 HG02074.hp1 others(9): Show |
intron_variant | MODIFIER | c.1185+746dupA | MFSD11 | ENSG00000092931.12 | transcript | ENST00000685175.1 | protein_coding | 12/12 | INFO_REALIGN_3_PRIME | chr17 | 76777267 | ||||||
| chr17:76777267 | CA | C | 11 | a0001c0001t0002g0112 a0001c0001t0005g0035 a0001c0001t0005g0036 others(8): Show |
12 | HG00558.hp1 HG01243.hp1 HG01884.hp1 others(9): Show |
intron_variant | MODIFIER | c.1185+746delA | MFSD11 | ENSG00000092931.12 | transcript | ENST00000685175.1 | protein_coding | 12/12 | INFO_REALIGN_3_PRIME | chr17 | 76777267 | ||||||
| chr17:76777267 | CAAAAAAA others(4): Show |
C | 2 | a0001c0006t0007g0042 a0001c0006t0007g0043 |
2 | HG02602.hp1 HG02735.hp1 |
intron_variant | MODIFIER | c.1185+736_1185+746d others(13): Show |
MFSD11 | ENSG00000092931.12 | transcript | ENST00000685175.1 | protein_coding | 12/12 | INFO_REALIGN_3_PRIME | chr17 | 76777267 | ||||||
| chr17:76777328 | C | T | 2 | a0001c0006t0007g0042 a0001c0006t0007g0043 |
2 | HG02602.hp1 HG02735.hp1 |
intron_variant | MODIFIER | c.1185+787C>T | MFSD11 | ENSG00000092931.12 | transcript | ENST00000685175.1 | protein_coding | 12/12 | chr17 | 76777328 | |||||||
| chr17:76777466 | C | A | 9 | a0001c0001t0005g0035 a0001c0001t0005g0036 a0001c0001t0005g0037 others(6): Show |
10 | HG01243.hp1 HG01884.hp1 HG02622.hp2 others(7): Show |
intron_variant | MODIFIER | c.1186-722C>A | MFSD11 | ENSG00000092931.12 | transcript | ENST00000685175.1 | protein_coding | 12/12 | chr17 | 76777466 | |||||||
| chr17:76777530 | G | A | 1 | a0001c0001t0002g0108 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.1186-658G>A | MFSD11 | ENSG00000092931.12 | transcript | ENST00000685175.1 | protein_coding | 12/12 | chr17 | 76777530 | |||||||
| chr17:76777573 | C | CT | 13 | a0001c0001t0001g0105 a0001c0001t0001g0130 a0001c0001t0004g0012 others(10): Show |
13 | HG01069.hp1 HG01099.hp1 HG01884.hp2 others(10): Show |
intron_variant | MODIFIER | c.1186-606dupT | MFSD11 | ENSG00000092931.12 | transcript | ENST00000685175.1 | protein_coding | 12/12 | INFO_REALIGN_3_PRIME | chr17 | 76777573 | ||||||
| chr17:76778157 | G | A | 22 | a0001c0001t0001g0105 a0001c0001t0001g0130 a0001c0001t0004g0012 others(19): Show |
23 | HG01069.hp1 HG01099.hp1 HG01243.hp1 others(20): Show |
intron_variant | MODIFIER | c.1186-31G>A | MFSD11 | ENSG00000092931.12 | transcript | ENST00000685175.1 | protein_coding | 12/12 | chr17 | 76778157 | |||||||
| chr17:76778161 | G | A | 1 | a0001c0001t0001g0258 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.1186-27G>A | MFSD11 | ENSG00000092931.12 | transcript | ENST00000685175.1 | protein_coding | 12/12 | chr17 | 76778161 | |||||||
| chr17:76778176 | G | A | 3 | a0001c0001t0001g0130 a0001c0004t0001g0100 a0001c0004t0001g0131 |
3 | HG02145.hp2 NA18522.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.1186-12G>A | MFSD11 | ENSG00000092931.12 | transcript | ENST00000685175.1 | protein_coding | 12/12 | chr17 | 76778176 |