Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 64747 |
| ensemblid | ENSG00000118855.21 |
| hgncid | 25874 |
| symbol | MFSD1 |
| name | major facilitator superfamily domain containing 1 |
| refseq_nuc | NM_022736.4 |
| refseq_prot | NP_073573.3 |
| ensembl_nuc | ENST00000415822.8 |
| ensembl_prot | ENSP00000403117.3 |
| mane_status | MANE Select |
| chr | chr3 |
| start | 158802054 |
| end | 158829716 |
| strand | + |
| ver | v1.2 |
| region | chr3:158802054-158829716 |
| region5000 | chr3:158797054-158834716 |
| regionname0 | MFSD1_chr3_158802054_158829716 |
| regionname5000 | MFSD1_chr3_158797054_158834716 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/0 | 464 | 174 | 26 | 32 | 88 | 6 | 21 | 64 | MFSD1_chr3_158797054_158834716 | MFSD1 | MEEED others(459): Show |
chr3 | 158797054 | 158834716 |
| a0002 | 0/1 | 464 | 157 | 57 | 32 | 42 | 7 | 18 | 34 | MFSD1_chr3_158797054_158834716 | MFSD1 | MEEED others(459): Show |
chr3 | 158797054 | 158834716 |
| a0003 | 0/0 | 464 | 61 | 5 | 11 | 42 | 1 | 2 | 35 | MFSD1_chr3_158797054_158834716 | MFSD1 | MEEED others(459): Show |
chr3 | 158797054 | 158834716 |
| a0004 | 0/0 | 464 | 5 | 4 | 1 | 0 | 0 | 0 | 0 | MFSD1_chr3_158797054_158834716 | MFSD1 | MEEED others(459): Show |
chr3 | 158797054 | 158834716 |
| a0005 | 0/0 | 464 | 2 | 0 | 0 | 1 | 0 | 1 | 0 | MFSD1_chr3_158797054_158834716 | MFSD1 | MEEED others(459): Show |
chr3 | 158797054 | 158834716 |
| a0006 | 0/0 | 464 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | MFSD1_chr3_158797054_158834716 | MFSD1 | MEEED others(459): Show |
chr3 | 158797054 | 158834716 |
| a0007 | 0/0 | 464 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | MFSD1_chr3_158797054_158834716 | MFSD1 | MEEED others(459): Show |
chr3 | 158797054 | 158834716 |
| a0008 | 0/0 | 464 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | MFSD1_chr3_158797054_158834716 | MFSD1 | MEEED others(459): Show |
chr3 | 158797054 | 158834716 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/0 | 1394 | 173 | 26 | 31 | 88 | 6 | 21 | MFSD1_chr3_158797054_158834716 | MFSD1 | ATGGA others(1389): Show |
chr3 | 158797054 | 158834716 | ||
| a0001c0007 | 0/0 | 1394 | 1 | 0 | 1 | 0 | 0 | 0 | MFSD1_chr3_158797054_158834716 | MFSD1 | ATGGA others(1389): Show |
chr3 | 158797054 | 158834716 | ||
| a0002c0002 | 0/1 | 1394 | 101 | 52 | 25 | 13 | 2 | 8 | MFSD1_chr3_158797054_158834716 | MFSD1 | ATGGA others(1389): Show |
chr3 | 158797054 | 158834716 | ||
| a0002c0004 | 0/0 | 1394 | 55 | 5 | 7 | 29 | 5 | 9 | MFSD1_chr3_158797054_158834716 | MFSD1 | ATGGA others(1389): Show |
chr3 | 158797054 | 158834716 | ||
| a0002c0008 | 0/0 | 1394 | 1 | 0 | 0 | 0 | 0 | 1 | MFSD1_chr3_158797054_158834716 | MFSD1 | ATGGA others(1389): Show |
chr3 | 158797054 | 158834716 | ||
| a0003c0003 | 0/0 | 1394 | 61 | 5 | 11 | 42 | 1 | 2 | MFSD1_chr3_158797054_158834716 | MFSD1 | ATGGA others(1389): Show |
chr3 | 158797054 | 158834716 | ||
| a0004c0005 | 0/0 | 1394 | 5 | 4 | 1 | 0 | 0 | 0 | MFSD1_chr3_158797054_158834716 | MFSD1 | ATGGA others(1389): Show |
chr3 | 158797054 | 158834716 | ||
| a0005c0006 | 0/0 | 1394 | 2 | 0 | 0 | 1 | 0 | 1 | MFSD1_chr3_158797054_158834716 | MFSD1 | ATGGA others(1389): Show |
chr3 | 158797054 | 158834716 | ||
| a0006c0009 | 0/0 | 1394 | 1 | 1 | 0 | 0 | 0 | 0 | MFSD1_chr3_158797054_158834716 | MFSD1 | ATGGA others(1389): Show |
chr3 | 158797054 | 158834716 | ||
| a0007c0011 | 0/0 | 1394 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD1_chr3_158797054_158834716 | MFSD1 | ATGGA others(1389): Show |
chr3 | 158797054 | 158834716 | ||
| a0008c0010 | 0/0 | 1394 | 1 | 1 | 0 | 0 | 0 | 0 | MFSD1_chr3_158797054_158834716 | MFSD1 | ATGGA others(1389): Show |
chr3 | 158797054 | 158834716 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 1/0 | 2230 | 163 | 26 | 30 | 81 | 6 | 19 | MFSD1_chr3_158797054_158834716 | MFSD1 | AGTCA others(2225): Show |
chr3 | 158797054 | 158834716 |
| a0001c0001t0004 | 0/0 | 2230 | 4 | 0 | 0 | 4 | 0 | 0 | MFSD1_chr3_158797054_158834716 | MFSD1 | AGTCA others(2225): Show |
chr3 | 158797054 | 158834716 |
| a0001c0001t0006 | 0/0 | 2230 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD1_chr3_158797054_158834716 | MFSD1 | AGTCA others(2225): Show |
chr3 | 158797054 | 158834716 |
| a0001c0001t0007 | 0/0 | 2220 | 1 | 0 | 0 | 0 | 0 | 1 | MFSD1_chr3_158797054_158834716 | MFSD1 | AGTCA others(2215): Show |
chr3 | 158797054 | 158834716 |
| a0001c0001t0008 | 0/0 | 2230 | 1 | 0 | 0 | 0 | 0 | 1 | MFSD1_chr3_158797054_158834716 | MFSD1 | AGTCA others(2225): Show |
chr3 | 158797054 | 158834716 |
| a0001c0001t0009 | 0/0 | 2230 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD1_chr3_158797054_158834716 | MFSD1 | AGTCA others(2225): Show |
chr3 | 158797054 | 158834716 |
| a0001c0001t0011 | 0/0 | 2230 | 1 | 0 | 1 | 0 | 0 | 0 | MFSD1_chr3_158797054_158834716 | MFSD1 | AGTCA others(2225): Show |
chr3 | 158797054 | 158834716 |
| a0001c0001t0012 | 0/0 | 2626 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD1_chr3_158797054_158834716 | MFSD1 | AGTCA others(2621): Show |
chr3 | 158797054 | 158834716 |
| a0001c0007t0001 | 0/0 | 2230 | 1 | 0 | 1 | 0 | 0 | 0 | MFSD1_chr3_158797054_158834716 | MFSD1 | AGTCA others(2225): Show |
chr3 | 158797054 | 158834716 |
| a0002c0002t0001 | 0/0 | 2230 | 80 | 35 | 22 | 13 | 2 | 8 | MFSD1_chr3_158797054_158834716 | MFSD1 | AGTCA others(2225): Show |
chr3 | 158797054 | 158834716 |
| a0002c0002t0002 | 0/1 | 2231 | 2 | 1 | 0 | 0 | 0 | 0 | MFSD1_chr3_158797054_158834716 | MFSD1 | AGTCA others(2226): Show |
chr3 | 158797054 | 158834716 |
| a0002c0002t0003 | 0/0 | 2230 | 15 | 13 | 2 | 0 | 0 | 0 | MFSD1_chr3_158797054_158834716 | MFSD1 | AGTCA others(2225): Show |
chr3 | 158797054 | 158834716 |
| a0002c0002t0005 | 0/0 | 2230 | 3 | 3 | 0 | 0 | 0 | 0 | MFSD1_chr3_158797054_158834716 | MFSD1 | AGTCA others(2225): Show |
chr3 | 158797054 | 158834716 |
| a0002c0002t0010 | 0/0 | 2230 | 1 | 0 | 1 | 0 | 0 | 0 | MFSD1_chr3_158797054_158834716 | MFSD1 | AGTCA others(2225): Show |
chr3 | 158797054 | 158834716 |
| a0002c0004t0001 | 0/0 | 2230 | 55 | 5 | 7 | 29 | 5 | 9 | MFSD1_chr3_158797054_158834716 | MFSD1 | AGTCA others(2225): Show |
chr3 | 158797054 | 158834716 |
| a0002c0008t0001 | 0/0 | 2230 | 1 | 0 | 0 | 0 | 0 | 1 | MFSD1_chr3_158797054_158834716 | MFSD1 | AGTCA others(2225): Show |
chr3 | 158797054 | 158834716 |
| a0003c0003t0001 | 0/0 | 2230 | 4 | 2 | 2 | 0 | 0 | 0 | MFSD1_chr3_158797054_158834716 | MFSD1 | AGTCA others(2225): Show |
chr3 | 158797054 | 158834716 |
| a0003c0003t0002 | 0/0 | 2231 | 57 | 3 | 9 | 42 | 1 | 2 | MFSD1_chr3_158797054_158834716 | MFSD1 | AGTCA others(2226): Show |
chr3 | 158797054 | 158834716 |
| a0004c0005t0001 | 0/0 | 2230 | 5 | 4 | 1 | 0 | 0 | 0 | MFSD1_chr3_158797054_158834716 | MFSD1 | AGTCA others(2225): Show |
chr3 | 158797054 | 158834716 |
| a0005c0006t0001 | 0/0 | 2230 | 2 | 0 | 0 | 1 | 0 | 1 | MFSD1_chr3_158797054_158834716 | MFSD1 | AGTCA others(2225): Show |
chr3 | 158797054 | 158834716 |
| a0006c0009t0003 | 0/0 | 2230 | 1 | 1 | 0 | 0 | 0 | 0 | MFSD1_chr3_158797054_158834716 | MFSD1 | AGTCA others(2225): Show |
chr3 | 158797054 | 158834716 |
| a0007c0011t0013 | 0/0 | 2231 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD1_chr3_158797054_158834716 | MFSD1 | AGTCA others(2226): Show |
chr3 | 158797054 | 158834716 |
| a0008c0010t0001 | 0/0 | 2230 | 1 | 1 | 0 | 0 | 0 | 0 | MFSD1_chr3_158797054_158834716 | MFSD1 | AGTCA others(2225): Show |
chr3 | 158797054 | 158834716 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0003 | 0/0 | 12 | 1 | 3 | 6 | 1 | 1 | MFSD1_chr3_158797054_158834716 | MFSD1 | chr3 | 158797054 | 158834716 |
| a0001c0001t0001g0005 | 0/0 | 9 | 0 | 0 | 9 | 0 | 0 | MFSD1_chr3_158797054_158834716 | MFSD1 | chr3 | 158797054 | 158834716 |
| a0001c0001t0001g0007 | 0/0 | 5 | 0 | 1 | 4 | 0 | 0 | MFSD1_chr3_158797054_158834716 | MFSD1 | chr3 | 158797054 | 158834716 |
| a0001c0001t0001g0010 | 0/0 | 3 | 0 | 2 | 1 | 0 | 0 | MFSD1_chr3_158797054_158834716 | MFSD1 | chr3 | 158797054 | 158834716 |
| a0001c0001t0001g0011 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | MFSD1_chr3_158797054_158834716 | MFSD1 | chr3 | 158797054 | 158834716 |
| a0001c0001t0001g0012 | 0/0 | 4 | 0 | 2 | 2 | 0 | 0 | MFSD1_chr3_158797054_158834716 | MFSD1 | chr3 | 158797054 | 158834716 |
| a0001c0001t0001g0016 | 0/0 | 4 | 0 | 0 | 0 | 3 | 1 | MFSD1_chr3_158797054_158834716 | MFSD1 | chr3 | 158797054 | 158834716 |
| a0001c0001t0001g0018 | 0/0 | 3 | 0 | 2 | 0 | 0 | 1 | MFSD1_chr3_158797054_158834716 | MFSD1 | chr3 | 158797054 | 158834716 |
| a0001c0001t0001g0026 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | MFSD1_chr3_158797054_158834716 | MFSD1 | chr3 | 158797054 | 158834716 |
| a0001c0001t0001g0028 | 0/0 | 3 | 0 | 2 | 0 | 0 | 1 | MFSD1_chr3_158797054_158834716 | MFSD1 | chr3 | 158797054 | 158834716 |
| a0001c0001t0001g0029 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | MFSD1_chr3_158797054_158834716 | MFSD1 | chr3 | 158797054 | 158834716 |
| a0001c0001t0001g0030 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | MFSD1_chr3_158797054_158834716 | MFSD1 | chr3 | 158797054 | 158834716 |
| a0001c0001t0001g0031 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | MFSD1_chr3_158797054_158834716 | MFSD1 | chr3 | 158797054 | 158834716 |
| a0001c0001t0001g0032 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MFSD1_chr3_158797054_158834716 | MFSD1 | chr3 | 158797054 | 158834716 |
| a0001c0001t0001g0034 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | MFSD1_chr3_158797054_158834716 | MFSD1 | chr3 | 158797054 | 158834716 |
| a0001c0001t0001g0035 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | MFSD1_chr3_158797054_158834716 | MFSD1 | chr3 | 158797054 | 158834716 |
| a0001c0001t0001g0036 | 0/0 | 2 | 1 | 0 | 1 | 0 | 0 | MFSD1_chr3_158797054_158834716 | MFSD1 | chr3 | 158797054 | 158834716 |
| a0001c0001t0001g0037 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | MFSD1_chr3_158797054_158834716 | MFSD1 | chr3 | 158797054 | 158834716 |
| a0001c0001t0001g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD1_chr3_158797054_158834716 | MFSD1 | chr3 | 158797054 | 158834716 |
| a0001c0001t0001g0039 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | MFSD1_chr3_158797054_158834716 | MFSD1 | chr3 | 158797054 | 158834716 |
| a0001c0001t0001g0040 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | MFSD1_chr3_158797054_158834716 | MFSD1 | chr3 | 158797054 | 158834716 |
| a0001c0001t0001g0041 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MFSD1_chr3_158797054_158834716 | MFSD1 | chr3 | 158797054 | 158834716 |
| a0001c0001t0001g0042 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MFSD1_chr3_158797054_158834716 | MFSD1 | chr3 | 158797054 | 158834716 |
| a0001c0001t0001g0056 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MFSD1_chr3_158797054_158834716 | MFSD1 | chr3 | 158797054 | 158834716 |
| a0001c0001t0001g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFSD1_chr3_158797054_158834716 | MFSD1 | chr3 | 158797054 | 158834716 |
| a0001c0001t0001g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD1_chr3_158797054_158834716 | MFSD1 | chr3 | 158797054 | 158834716 |
| a0001c0001t0001g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD1_chr3_158797054_158834716 | MFSD1 | chr3 | 158797054 | 158834716 |
| a0001c0001t0001g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD1_chr3_158797054_158834716 | MFSD1 | chr3 | 158797054 | 158834716 |
| a0001c0001t0001g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD1_chr3_158797054_158834716 | MFSD1 | chr3 | 158797054 | 158834716 |
| a0001c0001t0001g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD1_chr3_158797054_158834716 | MFSD1 | chr3 | 158797054 | 158834716 |
| a0001c0001t0001g0066 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MFSD1_chr3_158797054_158834716 | MFSD1 | chr3 | 158797054 | 158834716 |
| a0001c0001t0001g0067 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MFSD1_chr3_158797054_158834716 | MFSD1 | chr3 | 158797054 | 158834716 |
| a0001c0001t0001g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD1_chr3_158797054_158834716 | MFSD1 | chr3 | 158797054 | 158834716 |
| a0001c0001t0001g0069 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MFSD1_chr3_158797054_158834716 | MFSD1 | chr3 | 158797054 | 158834716 |
| a0001c0001t0001g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD1_chr3_158797054_158834716 | MFSD1 | chr3 | 158797054 | 158834716 |
| a0001c0001t0001g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD1_chr3_158797054_158834716 | MFSD1 | chr3 | 158797054 | 158834716 |
| a0001c0001t0001g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD1_chr3_158797054_158834716 | MFSD1 | chr3 | 158797054 | 158834716 |
| a0001c0001t0001g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD1_chr3_158797054_158834716 | MFSD1 | chr3 | 158797054 | 158834716 |
| a0001c0001t0001g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD1_chr3_158797054_158834716 | MFSD1 | chr3 | 158797054 | 158834716 |
| a0001c0001t0001g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD1_chr3_158797054_158834716 | MFSD1 | chr3 | 158797054 | 158834716 |
| a0001c0001t0001g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD1_chr3_158797054_158834716 | MFSD1 | chr3 | 158797054 | 158834716 |
| a0001c0001t0001g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD1_chr3_158797054_158834716 | MFSD1 | chr3 | 158797054 | 158834716 |
| a0001c0001t0001g0079 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MFSD1_chr3_158797054_158834716 | MFSD1 | chr3 | 158797054 | 158834716 |
| a0001c0001t0001g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD1_chr3_158797054_158834716 | MFSD1 | chr3 | 158797054 | 158834716 |
| a0001c0001t0001g0081 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | MFSD1_chr3_158797054_158834716 | MFSD1 | chr3 | 158797054 | 158834716 |
| a0001c0001t0001g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD1_chr3_158797054_158834716 | MFSD1 | chr3 | 158797054 | 158834716 |
| a0001c0001t0001g0086 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MFSD1_chr3_158797054_158834716 | MFSD1 | chr3 | 158797054 | 158834716 |
| a0001c0001t0001g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD1_chr3_158797054_158834716 | MFSD1 | chr3 | 158797054 | 158834716 |
| a0001c0001t0001g0088 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MFSD1_chr3_158797054_158834716 | MFSD1 | chr3 | 158797054 | 158834716 |
| a0001c0001t0001g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD1_chr3_158797054_158834716 | MFSD1 | chr3 | 158797054 | 158834716 |
| a0001c0001t0001g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD1_chr3_158797054_158834716 | MFSD1 | chr3 | 158797054 | 158834716 |
| a0001c0001t0001g0092 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MFSD1_chr3_158797054_158834716 | MFSD1 | chr3 | 158797054 | 158834716 |
| a0001c0001t0001g0093 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MFSD1_chr3_158797054_158834716 | MFSD1 | chr3 | 158797054 | 158834716 |
| a0001c0001t0001g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD1_chr3_158797054_158834716 | MFSD1 | chr3 | 158797054 | 158834716 |
| a0001c0001t0001g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD1_chr3_158797054_158834716 | MFSD1 | chr3 | 158797054 | 158834716 |
| a0001c0001t0001g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD1_chr3_158797054_158834716 | MFSD1 | chr3 | 158797054 | 158834716 |
| a0001c0001t0001g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD1_chr3_158797054_158834716 | MFSD1 | chr3 | 158797054 | 158834716 |
| a0001c0001t0001g0098 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MFSD1_chr3_158797054_158834716 | MFSD1 | chr3 | 158797054 | 158834716 |
| a0001c0001t0001g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD1_chr3_158797054_158834716 | MFSD1 | chr3 | 158797054 | 158834716 |
| a0001c0001t0001g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD1_chr3_158797054_158834716 | MFSD1 | chr3 | 158797054 | 158834716 |
| a0001c0001t0001g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD1_chr3_158797054_158834716 | MFSD1 | chr3 | 158797054 | 158834716 |
| a0001c0001t0001g0103 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MFSD1_chr3_158797054_158834716 | MFSD1 | chr3 | 158797054 | 158834716 |
| a0001c0001t0001g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD1_chr3_158797054_158834716 | MFSD1 | chr3 | 158797054 | 158834716 |
| a0001c0001t0001g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD1_chr3_158797054_158834716 | MFSD1 | chr3 | 158797054 | 158834716 |
| a0001c0001t0001g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD1_chr3_158797054_158834716 | MFSD1 | chr3 | 158797054 | 158834716 |
| a0001c0001t0001g0108 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MFSD1_chr3_158797054_158834716 | MFSD1 | chr3 | 158797054 | 158834716 |
| a0001c0001t0001g0109 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MFSD1_chr3_158797054_158834716 | MFSD1 | chr3 | 158797054 | 158834716 |
| a0001c0001t0001g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD1_chr3_158797054_158834716 | MFSD1 | chr3 | 158797054 | 158834716 |
| a0001c0001t0001g0112 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MFSD1_chr3_158797054_158834716 | MFSD1 | chr3 | 158797054 | 158834716 |
| a0001c0001t0001g0113 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MFSD1_chr3_158797054_158834716 | MFSD1 | chr3 | 158797054 | 158834716 |
| a0001c0001t0001g0114 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MFSD1_chr3_158797054_158834716 | MFSD1 | chr3 | 158797054 | 158834716 |
| a0001c0001t0001g0115 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MFSD1_chr3_158797054_158834716 | MFSD1 | chr3 | 158797054 | 158834716 |
| a0001c0001t0001g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD1_chr3_158797054_158834716 | MFSD1 | chr3 | 158797054 | 158834716 |
| a0001c0001t0001g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD1_chr3_158797054_158834716 | MFSD1 | chr3 | 158797054 | 158834716 |
| a0001c0001t0001g0118 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MFSD1_chr3_158797054_158834716 | MFSD1 | chr3 | 158797054 | 158834716 |
| a0001c0001t0001g0119 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MFSD1_chr3_158797054_158834716 | MFSD1 | chr3 | 158797054 | 158834716 |
| a0001c0001t0001g0120 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MFSD1_chr3_158797054_158834716 | MFSD1 | chr3 | 158797054 | 158834716 |
| a0001c0001t0001g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD1_chr3_158797054_158834716 | MFSD1 | chr3 | 158797054 | 158834716 |
| a0001c0001t0001g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD1_chr3_158797054_158834716 | MFSD1 | chr3 | 158797054 | 158834716 |
| a0001c0001t0001g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD1_chr3_158797054_158834716 | MFSD1 | chr3 | 158797054 | 158834716 |
| a0001c0001t0001g0124 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MFSD1_chr3_158797054_158834716 | MFSD1 | chr3 | 158797054 | 158834716 |
| a0001c0001t0001g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD1_chr3_158797054_158834716 | MFSD1 | chr3 | 158797054 | 158834716 |
| a0001c0001t0001g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD1_chr3_158797054_158834716 | MFSD1 | chr3 | 158797054 | 158834716 |
| a0001c0001t0001g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD1_chr3_158797054_158834716 | MFSD1 | chr3 | 158797054 | 158834716 |
| a0001c0001t0001g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD1_chr3_158797054_158834716 | MFSD1 | chr3 | 158797054 | 158834716 |
| a0001c0001t0001g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD1_chr3_158797054_158834716 | MFSD1 | chr3 | 158797054 | 158834716 |
| a0001c0001t0001g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD1_chr3_158797054_158834716 | MFSD1 | chr3 | 158797054 | 158834716 |
| a0001c0001t0001g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD1_chr3_158797054_158834716 | MFSD1 | chr3 | 158797054 | 158834716 |
| a0001c0001t0001g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD1_chr3_158797054_158834716 | MFSD1 | chr3 | 158797054 | 158834716 |
| a0001c0001t0001g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFSD1_chr3_158797054_158834716 | MFSD1 | chr3 | 158797054 | 158834716 |
| a0001c0001t0001g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFSD1_chr3_158797054_158834716 | MFSD1 | chr3 | 158797054 | 158834716 |
| a0001c0001t0001g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFSD1_chr3_158797054_158834716 | MFSD1 | chr3 | 158797054 | 158834716 |
| a0001c0001t0001g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFSD1_chr3_158797054_158834716 | MFSD1 | chr3 | 158797054 | 158834716 |
| a0001c0001t0001g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD1_chr3_158797054_158834716 | MFSD1 | chr3 | 158797054 | 158834716 |
| a0001c0001t0001g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD1_chr3_158797054_158834716 | MFSD1 | chr3 | 158797054 | 158834716 |
| a0001c0001t0001g0157 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MFSD1_chr3_158797054_158834716 | MFSD1 | chr3 | 158797054 | 158834716 |
| a0001c0001t0001g0158 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MFSD1_chr3_158797054_158834716 | MFSD1 | chr3 | 158797054 | 158834716 |
| a0001c0001t0001g0159 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MFSD1_chr3_158797054_158834716 | MFSD1 | chr3 | 158797054 | 158834716 |
| a0001c0001t0001g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFSD1_chr3_158797054_158834716 | MFSD1 | chr3 | 158797054 | 158834716 |
| a0001c0001t0001g0226 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MFSD1_chr3_158797054_158834716 | MFSD1 | chr3 | 158797054 | 158834716 |
| a0001c0001t0001g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFSD1_chr3_158797054_158834716 | MFSD1 | chr3 | 158797054 | 158834716 |
| a0001c0001t0001g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFSD1_chr3_158797054_158834716 | MFSD1 | chr3 | 158797054 | 158834716 |
| a0001c0001t0001g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFSD1_chr3_158797054_158834716 | MFSD1 | chr3 | 158797054 | 158834716 |
| a0001c0001t0001g0234 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MFSD1_chr3_158797054_158834716 | MFSD1 | chr3 | 158797054 | 158834716 |
| a0001c0001t0001g0235 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MFSD1_chr3_158797054_158834716 | MFSD1 | chr3 | 158797054 | 158834716 |
| a0001c0001t0001g0236 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MFSD1_chr3_158797054_158834716 | MFSD1 | chr3 | 158797054 | 158834716 |
| a0001c0001t0001g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFSD1_chr3_158797054_158834716 | MFSD1 | chr3 | 158797054 | 158834716 |
| a0001c0001t0001g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFSD1_chr3_158797054_158834716 | MFSD1 | chr3 | 158797054 | 158834716 |
| a0001c0001t0004g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD1_chr3_158797054_158834716 | MFSD1 | chr3 | 158797054 | 158834716 |
| a0001c0001t0004g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD1_chr3_158797054_158834716 | MFSD1 | chr3 | 158797054 | 158834716 |
| a0001c0001t0004g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD1_chr3_158797054_158834716 | MFSD1 | chr3 | 158797054 | 158834716 |
| a0001c0001t0004g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD1_chr3_158797054_158834716 | MFSD1 | chr3 | 158797054 | 158834716 |
| a0001c0001t0006g0010 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD1_chr3_158797054_158834716 | MFSD1 | chr3 | 158797054 | 158834716 |
| a0001c0001t0007g0077 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MFSD1_chr3_158797054_158834716 | MFSD1 | chr3 | 158797054 | 158834716 |
| a0001c0001t0008g0211 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MFSD1_chr3_158797054_158834716 | MFSD1 | chr3 | 158797054 | 158834716 |
| a0001c0001t0009g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD1_chr3_158797054_158834716 | MFSD1 | chr3 | 158797054 | 158834716 |
| a0001c0001t0011g0106 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MFSD1_chr3_158797054_158834716 | MFSD1 | chr3 | 158797054 | 158834716 |
| a0001c0001t0012g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD1_chr3_158797054_158834716 | MFSD1 | chr3 | 158797054 | 158834716 |
| a0001c0007t0001g0161 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MFSD1_chr3_158797054_158834716 | MFSD1 | chr3 | 158797054 | 158834716 |
| a0002c0002t0001g0008 | 0/0 | 5 | 0 | 0 | 4 | 0 | 1 | MFSD1_chr3_158797054_158834716 | MFSD1 | chr3 | 158797054 | 158834716 |
| a0002c0002t0001g0009 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | MFSD1_chr3_158797054_158834716 | MFSD1 | chr3 | 158797054 | 158834716 |
| a0002c0002t0001g0013 | 0/0 | 4 | 1 | 1 | 1 | 0 | 1 | MFSD1_chr3_158797054_158834716 | MFSD1 | chr3 | 158797054 | 158834716 |
| a0002c0002t0001g0014 | 0/0 | 4 | 1 | 2 | 0 | 0 | 1 | MFSD1_chr3_158797054_158834716 | MFSD1 | chr3 | 158797054 | 158834716 |
| a0002c0002t0001g0017 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | MFSD1_chr3_158797054_158834716 | MFSD1 | chr3 | 158797054 | 158834716 |
| a0002c0002t0001g0024 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | MFSD1_chr3_158797054_158834716 | MFSD1 | chr3 | 158797054 | 158834716 |
| a0002c0002t0001g0025 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | MFSD1_chr3_158797054_158834716 | MFSD1 | chr3 | 158797054 | 158834716 |
| a0002c0002t0001g0027 | 0/0 | 3 | 0 | 2 | 0 | 0 | 1 | MFSD1_chr3_158797054_158834716 | MFSD1 | chr3 | 158797054 | 158834716 |
| a0002c0002t0001g0051 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | MFSD1_chr3_158797054_158834716 | MFSD1 | chr3 | 158797054 | 158834716 |
| a0002c0002t0001g0052 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | MFSD1_chr3_158797054_158834716 | MFSD1 | chr3 | 158797054 | 158834716 |
| a0002c0002t0001g0053 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | MFSD1_chr3_158797054_158834716 | MFSD1 | chr3 | 158797054 | 158834716 |
| a0002c0002t0001g0054 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | MFSD1_chr3_158797054_158834716 | MFSD1 | chr3 | 158797054 | 158834716 |
| a0002c0002t0001g0057 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MFSD1_chr3_158797054_158834716 | MFSD1 | chr3 | 158797054 | 158834716 |
| a0002c0002t0001g0125 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MFSD1_chr3_158797054_158834716 | MFSD1 | chr3 | 158797054 | 158834716 |
| a0002c0002t0001g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD1_chr3_158797054_158834716 | MFSD1 | chr3 | 158797054 | 158834716 |
| a0002c0002t0001g0138 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MFSD1_chr3_158797054_158834716 | MFSD1 | chr3 | 158797054 | 158834716 |
| a0002c0002t0001g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFSD1_chr3_158797054_158834716 | MFSD1 | chr3 | 158797054 | 158834716 |
| a0002c0002t0001g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD1_chr3_158797054_158834716 | MFSD1 | chr3 | 158797054 | 158834716 |
| a0002c0002t0001g0188 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MFSD1_chr3_158797054_158834716 | MFSD1 | chr3 | 158797054 | 158834716 |
| a0002c0002t0001g0189 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MFSD1_chr3_158797054_158834716 | MFSD1 | chr3 | 158797054 | 158834716 |
| a0002c0002t0001g0190 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MFSD1_chr3_158797054_158834716 | MFSD1 | chr3 | 158797054 | 158834716 |
| a0002c0002t0001g0191 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MFSD1_chr3_158797054_158834716 | MFSD1 | chr3 | 158797054 | 158834716 |
| a0002c0002t0001g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFSD1_chr3_158797054_158834716 | MFSD1 | chr3 | 158797054 | 158834716 |
| a0002c0002t0001g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFSD1_chr3_158797054_158834716 | MFSD1 | chr3 | 158797054 | 158834716 |
| a0002c0002t0001g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFSD1_chr3_158797054_158834716 | MFSD1 | chr3 | 158797054 | 158834716 |
| a0002c0002t0001g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFSD1_chr3_158797054_158834716 | MFSD1 | chr3 | 158797054 | 158834716 |
| a0002c0002t0001g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFSD1_chr3_158797054_158834716 | MFSD1 | chr3 | 158797054 | 158834716 |
| a0002c0002t0001g0202 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MFSD1_chr3_158797054_158834716 | MFSD1 | chr3 | 158797054 | 158834716 |
| a0002c0002t0001g0203 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MFSD1_chr3_158797054_158834716 | MFSD1 | chr3 | 158797054 | 158834716 |
| a0002c0002t0001g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD1_chr3_158797054_158834716 | MFSD1 | chr3 | 158797054 | 158834716 |
| a0002c0002t0001g0205 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MFSD1_chr3_158797054_158834716 | MFSD1 | chr3 | 158797054 | 158834716 |
| a0002c0002t0001g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFSD1_chr3_158797054_158834716 | MFSD1 | chr3 | 158797054 | 158834716 |
| a0002c0002t0001g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFSD1_chr3_158797054_158834716 | MFSD1 | chr3 | 158797054 | 158834716 |
| a0002c0002t0001g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFSD1_chr3_158797054_158834716 | MFSD1 | chr3 | 158797054 | 158834716 |
| a0002c0002t0001g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFSD1_chr3_158797054_158834716 | MFSD1 | chr3 | 158797054 | 158834716 |
| a0002c0002t0001g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFSD1_chr3_158797054_158834716 | MFSD1 | chr3 | 158797054 | 158834716 |
| a0002c0002t0001g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFSD1_chr3_158797054_158834716 | MFSD1 | chr3 | 158797054 | 158834716 |
| a0002c0002t0001g0214 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MFSD1_chr3_158797054_158834716 | MFSD1 | chr3 | 158797054 | 158834716 |
| a0002c0002t0001g0215 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MFSD1_chr3_158797054_158834716 | MFSD1 | chr3 | 158797054 | 158834716 |
| a0002c0002t0001g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFSD1_chr3_158797054_158834716 | MFSD1 | chr3 | 158797054 | 158834716 |
| a0002c0002t0001g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFSD1_chr3_158797054_158834716 | MFSD1 | chr3 | 158797054 | 158834716 |
| a0002c0002t0001g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFSD1_chr3_158797054_158834716 | MFSD1 | chr3 | 158797054 | 158834716 |
| a0002c0002t0001g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFSD1_chr3_158797054_158834716 | MFSD1 | chr3 | 158797054 | 158834716 |
| a0002c0002t0001g0220 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MFSD1_chr3_158797054_158834716 | MFSD1 | chr3 | 158797054 | 158834716 |
| a0002c0002t0001g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFSD1_chr3_158797054_158834716 | MFSD1 | chr3 | 158797054 | 158834716 |
| a0002c0002t0001g0227 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MFSD1_chr3_158797054_158834716 | MFSD1 | chr3 | 158797054 | 158834716 |
| a0002c0002t0001g0228 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MFSD1_chr3_158797054_158834716 | MFSD1 | chr3 | 158797054 | 158834716 |
| a0002c0002t0001g0229 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MFSD1_chr3_158797054_158834716 | MFSD1 | chr3 | 158797054 | 158834716 |
| a0002c0002t0001g0233 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MFSD1_chr3_158797054_158834716 | MFSD1 | chr3 | 158797054 | 158834716 |
| a0002c0002t0001g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFSD1_chr3_158797054_158834716 | MFSD1 | chr3 | 158797054 | 158834716 |
| a0002c0002t0001g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFSD1_chr3_158797054_158834716 | MFSD1 | chr3 | 158797054 | 158834716 |
| a0002c0002t0001g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFSD1_chr3_158797054_158834716 | MFSD1 | chr3 | 158797054 | 158834716 |
| a0002c0002t0002g0133 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | MFSD1_chr3_158797054_158834716 | MFSD1 | chr3 | 158797054 | 158834716 |
| a0002c0002t0002g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFSD1_chr3_158797054_158834716 | MFSD1 | chr3 | 158797054 | 158834716 |
| a0002c0002t0003g0015 | 0/0 | 4 | 3 | 1 | 0 | 0 | 0 | MFSD1_chr3_158797054_158834716 | MFSD1 | chr3 | 158797054 | 158834716 |
| a0002c0002t0003g0019 | 0/0 | 3 | 2 | 1 | 0 | 0 | 0 | MFSD1_chr3_158797054_158834716 | MFSD1 | chr3 | 158797054 | 158834716 |
| a0002c0002t0003g0020 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | MFSD1_chr3_158797054_158834716 | MFSD1 | chr3 | 158797054 | 158834716 |
| a0002c0002t0003g0043 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MFSD1_chr3_158797054_158834716 | MFSD1 | chr3 | 158797054 | 158834716 |
| a0002c0002t0003g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFSD1_chr3_158797054_158834716 | MFSD1 | chr3 | 158797054 | 158834716 |
| a0002c0002t0003g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFSD1_chr3_158797054_158834716 | MFSD1 | chr3 | 158797054 | 158834716 |
| a0002c0002t0003g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFSD1_chr3_158797054_158834716 | MFSD1 | chr3 | 158797054 | 158834716 |
| a0002c0002t0005g0044 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MFSD1_chr3_158797054_158834716 | MFSD1 | chr3 | 158797054 | 158834716 |
| a0002c0002t0005g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFSD1_chr3_158797054_158834716 | MFSD1 | chr3 | 158797054 | 158834716 |
| a0002c0002t0010g0139 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MFSD1_chr3_158797054_158834716 | MFSD1 | chr3 | 158797054 | 158834716 |
| a0002c0004t0001g0001 | 0/0 | 21 | 1 | 2 | 13 | 1 | 4 | MFSD1_chr3_158797054_158834716 | MFSD1 | chr3 | 158797054 | 158834716 |
| a0002c0004t0001g0006 | 0/0 | 5 | 1 | 0 | 4 | 0 | 0 | MFSD1_chr3_158797054_158834716 | MFSD1 | chr3 | 158797054 | 158834716 |
| a0002c0004t0001g0022 | 0/0 | 3 | 0 | 1 | 0 | 1 | 1 | MFSD1_chr3_158797054_158834716 | MFSD1 | chr3 | 158797054 | 158834716 |
| a0002c0004t0001g0033 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MFSD1_chr3_158797054_158834716 | MFSD1 | chr3 | 158797054 | 158834716 |
| a0002c0004t0001g0045 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | MFSD1_chr3_158797054_158834716 | MFSD1 | chr3 | 158797054 | 158834716 |
| a0002c0004t0001g0046 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MFSD1_chr3_158797054_158834716 | MFSD1 | chr3 | 158797054 | 158834716 |
| a0002c0004t0001g0055 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | MFSD1_chr3_158797054_158834716 | MFSD1 | chr3 | 158797054 | 158834716 |
| a0002c0004t0001g0062 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MFSD1_chr3_158797054_158834716 | MFSD1 | chr3 | 158797054 | 158834716 |
| a0002c0004t0001g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD1_chr3_158797054_158834716 | MFSD1 | chr3 | 158797054 | 158834716 |
| a0002c0004t0001g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD1_chr3_158797054_158834716 | MFSD1 | chr3 | 158797054 | 158834716 |
| a0002c0004t0001g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFSD1_chr3_158797054_158834716 | MFSD1 | chr3 | 158797054 | 158834716 |
| a0002c0004t0001g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD1_chr3_158797054_158834716 | MFSD1 | chr3 | 158797054 | 158834716 |
| a0002c0004t0001g0149 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MFSD1_chr3_158797054_158834716 | MFSD1 | chr3 | 158797054 | 158834716 |
| a0002c0004t0001g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD1_chr3_158797054_158834716 | MFSD1 | chr3 | 158797054 | 158834716 |
| a0002c0004t0001g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD1_chr3_158797054_158834716 | MFSD1 | chr3 | 158797054 | 158834716 |
| a0002c0004t0001g0155 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MFSD1_chr3_158797054_158834716 | MFSD1 | chr3 | 158797054 | 158834716 |
| a0002c0004t0001g0156 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MFSD1_chr3_158797054_158834716 | MFSD1 | chr3 | 158797054 | 158834716 |
| a0002c0004t0001g0160 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MFSD1_chr3_158797054_158834716 | MFSD1 | chr3 | 158797054 | 158834716 |
| a0002c0004t0001g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFSD1_chr3_158797054_158834716 | MFSD1 | chr3 | 158797054 | 158834716 |
| a0002c0004t0001g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD1_chr3_158797054_158834716 | MFSD1 | chr3 | 158797054 | 158834716 |
| a0002c0004t0001g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD1_chr3_158797054_158834716 | MFSD1 | chr3 | 158797054 | 158834716 |
| a0002c0004t0001g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD1_chr3_158797054_158834716 | MFSD1 | chr3 | 158797054 | 158834716 |
| a0002c0004t0001g0193 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MFSD1_chr3_158797054_158834716 | MFSD1 | chr3 | 158797054 | 158834716 |
| a0002c0004t0001g0194 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MFSD1_chr3_158797054_158834716 | MFSD1 | chr3 | 158797054 | 158834716 |
| a0002c0004t0001g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFSD1_chr3_158797054_158834716 | MFSD1 | chr3 | 158797054 | 158834716 |
| a0002c0008t0001g0221 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MFSD1_chr3_158797054_158834716 | MFSD1 | chr3 | 158797054 | 158834716 |
| a0003c0003t0001g0049 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | MFSD1_chr3_158797054_158834716 | MFSD1 | chr3 | 158797054 | 158834716 |
| a0003c0003t0001g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFSD1_chr3_158797054_158834716 | MFSD1 | chr3 | 158797054 | 158834716 |
| a0003c0003t0001g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFSD1_chr3_158797054_158834716 | MFSD1 | chr3 | 158797054 | 158834716 |
| a0003c0003t0002g0002 | 0/0 | 19 | 0 | 5 | 13 | 0 | 1 | MFSD1_chr3_158797054_158834716 | MFSD1 | chr3 | 158797054 | 158834716 |
| a0003c0003t0002g0004 | 0/0 | 11 | 0 | 0 | 11 | 0 | 0 | MFSD1_chr3_158797054_158834716 | MFSD1 | chr3 | 158797054 | 158834716 |
| a0003c0003t0002g0021 | 0/0 | 3 | 0 | 2 | 0 | 1 | 0 | MFSD1_chr3_158797054_158834716 | MFSD1 | chr3 | 158797054 | 158834716 |
| a0003c0003t0002g0047 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MFSD1_chr3_158797054_158834716 | MFSD1 | chr3 | 158797054 | 158834716 |
| a0003c0003t0002g0048 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MFSD1_chr3_158797054_158834716 | MFSD1 | chr3 | 158797054 | 158834716 |
| a0003c0003t0002g0050 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MFSD1_chr3_158797054_158834716 | MFSD1 | chr3 | 158797054 | 158834716 |
| a0003c0003t0002g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD1_chr3_158797054_158834716 | MFSD1 | chr3 | 158797054 | 158834716 |
| a0003c0003t0002g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD1_chr3_158797054_158834716 | MFSD1 | chr3 | 158797054 | 158834716 |
| a0003c0003t0002g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD1_chr3_158797054_158834716 | MFSD1 | chr3 | 158797054 | 158834716 |
| a0003c0003t0002g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD1_chr3_158797054_158834716 | MFSD1 | chr3 | 158797054 | 158834716 |
| a0003c0003t0002g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFSD1_chr3_158797054_158834716 | MFSD1 | chr3 | 158797054 | 158834716 |
| a0003c0003t0002g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD1_chr3_158797054_158834716 | MFSD1 | chr3 | 158797054 | 158834716 |
| a0003c0003t0002g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFSD1_chr3_158797054_158834716 | MFSD1 | chr3 | 158797054 | 158834716 |
| a0003c0003t0002g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD1_chr3_158797054_158834716 | MFSD1 | chr3 | 158797054 | 158834716 |
| a0003c0003t0002g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD1_chr3_158797054_158834716 | MFSD1 | chr3 | 158797054 | 158834716 |
| a0003c0003t0002g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD1_chr3_158797054_158834716 | MFSD1 | chr3 | 158797054 | 158834716 |
| a0003c0003t0002g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD1_chr3_158797054_158834716 | MFSD1 | chr3 | 158797054 | 158834716 |
| a0003c0003t0002g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD1_chr3_158797054_158834716 | MFSD1 | chr3 | 158797054 | 158834716 |
| a0003c0003t0002g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD1_chr3_158797054_158834716 | MFSD1 | chr3 | 158797054 | 158834716 |
| a0003c0003t0002g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD1_chr3_158797054_158834716 | MFSD1 | chr3 | 158797054 | 158834716 |
| a0003c0003t0002g0184 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MFSD1_chr3_158797054_158834716 | MFSD1 | chr3 | 158797054 | 158834716 |
| a0003c0003t0002g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFSD1_chr3_158797054_158834716 | MFSD1 | chr3 | 158797054 | 158834716 |
| a0003c0003t0002g0186 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MFSD1_chr3_158797054_158834716 | MFSD1 | chr3 | 158797054 | 158834716 |
| a0003c0003t0002g0187 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MFSD1_chr3_158797054_158834716 | MFSD1 | chr3 | 158797054 | 158834716 |
| a0004c0005t0001g0023 | 0/0 | 3 | 2 | 1 | 0 | 0 | 0 | MFSD1_chr3_158797054_158834716 | MFSD1 | chr3 | 158797054 | 158834716 |
| a0004c0005t0001g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFSD1_chr3_158797054_158834716 | MFSD1 | chr3 | 158797054 | 158834716 |
| a0004c0005t0001g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFSD1_chr3_158797054_158834716 | MFSD1 | chr3 | 158797054 | 158834716 |
| a0005c0006t0001g0178 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MFSD1_chr3_158797054_158834716 | MFSD1 | chr3 | 158797054 | 158834716 |
| a0005c0006t0001g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD1_chr3_158797054_158834716 | MFSD1 | chr3 | 158797054 | 158834716 |
| a0006c0009t0003g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFSD1_chr3_158797054_158834716 | MFSD1 | chr3 | 158797054 | 158834716 |
| a0007c0011t0013g0004 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD1_chr3_158797054_158834716 | MFSD1 | chr3 | 158797054 | 158834716 |
| a0008c0010t0001g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFSD1_chr3_158797054_158834716 | MFSD1 | chr3 | 158797054 | 158834716 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0002 | c0004 | t0001 | g0160 | EUR | GBR | MFSD1_chr3_158797054_158834716 | MFSD1 | chr3 | 158797054 | 158834716 |
| HG00099 | hp2 | a0001 | c0001 | t0001 | g0040 | EUR | GBR | MFSD1_chr3_158797054_158834716 | MFSD1 | chr3 | 158797054 | 158834716 |
| HG00140 | hp1 | a0001 | c0001 | t0001 | g0016 | EUR | GBR | MFSD1_chr3_158797054_158834716 | MFSD1 | chr3 | 158797054 | 158834716 |
| HG00140 | hp2 | a0002 | c0004 | t0001 | g0156 | EUR | GBR | MFSD1_chr3_158797054_158834716 | MFSD1 | chr3 | 158797054 | 158834716 |
| HG00280 | hp1 | a0003 | c0003 | t0002 | g0021 | EUR | FIN | MFSD1_chr3_158797054_158834716 | MFSD1 | chr3 | 158797054 | 158834716 |
| HG00280 | hp2 | a0001 | c0001 | t0001 | g0003 | EUR | FIN | MFSD1_chr3_158797054_158834716 | MFSD1 | chr3 | 158797054 | 158834716 |
| HG00323 | hp1 | a0002 | c0004 | t0001 | g0193 | EUR | FIN | MFSD1_chr3_158797054_158834716 | MFSD1 | chr3 | 158797054 | 158834716 |
| HG00323 | hp2 | a0001 | c0001 | t0001 | g0119 | EUR | FIN | MFSD1_chr3_158797054_158834716 | MFSD1 | chr3 | 158797054 | 158834716 |
| HG00408 | hp1 | a0001 | c0001 | t0006 | g0010 | EAS | CHS | MFSD1_chr3_158797054_158834716 | MFSD1 | chr3 | 158797054 | 158834716 |
| HG00408 | hp2 | a0001 | c0001 | t0001 | g0011 | EAS | CHS | MFSD1_chr3_158797054_158834716 | MFSD1 | chr3 | 158797054 | 158834716 |
| HG00423 | hp1 | a0001 | c0001 | t0001 | g0011 | EAS | CHS | MFSD1_chr3_158797054_158834716 | MFSD1 | chr3 | 158797054 | 158834716 |
| HG00423 | hp2 | a0003 | c0003 | t0002 | g0004 | EAS | CHS | MFSD1_chr3_158797054_158834716 | MFSD1 | chr3 | 158797054 | 158834716 |
| HG00558 | hp1 | a0001 | c0001 | t0001 | g0116 | EAS | CHS | MFSD1_chr3_158797054_158834716 | MFSD1 | chr3 | 158797054 | 158834716 |
| HG00558 | hp2 | a0001 | c0001 | t0001 | g0061 | EAS | CHS | MFSD1_chr3_158797054_158834716 | MFSD1 | chr3 | 158797054 | 158834716 |
| HG00609 | hp1 | a0001 | c0001 | t0001 | g0042 | EAS | CHS | MFSD1_chr3_158797054_158834716 | MFSD1 | chr3 | 158797054 | 158834716 |
| HG00609 | hp2 | a0003 | c0003 | t0002 | g0048 | EAS | CHS | MFSD1_chr3_158797054_158834716 | MFSD1 | chr3 | 158797054 | 158834716 |
| HG00621 | hp1 | a0001 | c0001 | t0001 | g0129 | EAS | CHS | MFSD1_chr3_158797054_158834716 | MFSD1 | chr3 | 158797054 | 158834716 |
| HG00621 | hp2 | a0001 | c0001 | t0001 | g0007 | EAS | CHS | MFSD1_chr3_158797054_158834716 | MFSD1 | chr3 | 158797054 | 158834716 |
| HG00639 | hp1 | a0002 | c0002 | t0001 | g0205 | AMR | PUR | MFSD1_chr3_158797054_158834716 | MFSD1 | chr3 | 158797054 | 158834716 |
| HG00639 | hp2 | a0001 | c0001 | t0001 | g0028 | AMR | PUR | MFSD1_chr3_158797054_158834716 | MFSD1 | chr3 | 158797054 | 158834716 |
| HG00642 | hp1 | a0002 | c0002 | t0001 | g0202 | AMR | PUR | MFSD1_chr3_158797054_158834716 | MFSD1 | chr3 | 158797054 | 158834716 |
| HG00642 | hp2 | a0002 | c0002 | t0001 | g0220 | AMR | PUR | MFSD1_chr3_158797054_158834716 | MFSD1 | chr3 | 158797054 | 158834716 |
| HG00673 | hp1 | a0001 | c0001 | t0001 | g0152 | EAS | CHS | MFSD1_chr3_158797054_158834716 | MFSD1 | chr3 | 158797054 | 158834716 |
| HG00673 | hp2 | a0001 | c0001 | t0001 | g0007 | EAS | CHS | MFSD1_chr3_158797054_158834716 | MFSD1 | chr3 | 158797054 | 158834716 |
| HG00733 | hp1 | a0002 | c0004 | t0001 | g0001 | AMR | PUR | MFSD1_chr3_158797054_158834716 | MFSD1 | chr3 | 158797054 | 158834716 |
| HG00733 | hp2 | a0001 | c0001 | t0001 | g0236 | AMR | PUR | MFSD1_chr3_158797054_158834716 | MFSD1 | chr3 | 158797054 | 158834716 |
| HG00735 | hp1 | a0001 | c0001 | t0001 | g0003 | AMR | PUR | MFSD1_chr3_158797054_158834716 | MFSD1 | chr3 | 158797054 | 158834716 |
| HG00735 | hp2 | a0002 | c0002 | t0001 | g0027 | AMR | PUR | MFSD1_chr3_158797054_158834716 | MFSD1 | chr3 | 158797054 | 158834716 |
| HG00738 | hp1 | a0002 | c0002 | t0001 | g0051 | AMR | PUR | MFSD1_chr3_158797054_158834716 | MFSD1 | chr3 | 158797054 | 158834716 |
| HG00738 | hp2 | a0001 | c0001 | t0001 | g0012 | AMR | PUR | MFSD1_chr3_158797054_158834716 | MFSD1 | chr3 | 158797054 | 158834716 |
| HG00741 | hp1 | a0002 | c0004 | t0001 | g0022 | AMR | PUR | MFSD1_chr3_158797054_158834716 | MFSD1 | chr3 | 158797054 | 158834716 |
| HG00741 | hp2 | a0002 | c0002 | t0001 | g0228 | AMR | PUR | MFSD1_chr3_158797054_158834716 | MFSD1 | chr3 | 158797054 | 158834716 |
| HG01069 | hp1 | a0002 | c0002 | t0001 | g0203 | AMR | PUR | MFSD1_chr3_158797054_158834716 | MFSD1 | chr3 | 158797054 | 158834716 |
| HG01069 | hp2 | a0003 | c0003 | t0002 | g0187 | AMR | PUR | MFSD1_chr3_158797054_158834716 | MFSD1 | chr3 | 158797054 | 158834716 |
| HG01070 | hp1 | a0003 | c0003 | t0002 | g0002 | AMR | PUR | MFSD1_chr3_158797054_158834716 | MFSD1 | chr3 | 158797054 | 158834716 |
| HG01070 | hp2 | a0001 | c0001 | t0001 | g0028 | AMR | PUR | MFSD1_chr3_158797054_158834716 | MFSD1 | chr3 | 158797054 | 158834716 |
| HG01071 | hp1 | a0002 | c0002 | t0001 | g0052 | AMR | PUR | MFSD1_chr3_158797054_158834716 | MFSD1 | chr3 | 158797054 | 158834716 |
| HG01071 | hp2 | a0003 | c0003 | t0002 | g0002 | AMR | PUR | MFSD1_chr3_158797054_158834716 | MFSD1 | chr3 | 158797054 | 158834716 |
| HG01074 | hp1 | a0002 | c0002 | t0001 | g0053 | AMR | PUR | MFSD1_chr3_158797054_158834716 | MFSD1 | chr3 | 158797054 | 158834716 |
| HG01074 | hp2 | a0003 | c0003 | t0002 | g0021 | AMR | PUR | MFSD1_chr3_158797054_158834716 | MFSD1 | chr3 | 158797054 | 158834716 |
| HG01081 | hp1 | a0002 | c0004 | t0001 | g0062 | AMR | PUR | MFSD1_chr3_158797054_158834716 | MFSD1 | chr3 | 158797054 | 158834716 |
| HG01081 | hp2 | a0003 | c0003 | t0002 | g0186 | AMR | PUR | MFSD1_chr3_158797054_158834716 | MFSD1 | chr3 | 158797054 | 158834716 |
| HG01099 | hp1 | a0003 | c0003 | t0002 | g0021 | AMR | PUR | MFSD1_chr3_158797054_158834716 | MFSD1 | chr3 | 158797054 | 158834716 |
| HG01099 | hp2 | a0002 | c0002 | t0001 | g0014 | AMR | PUR | MFSD1_chr3_158797054_158834716 | MFSD1 | chr3 | 158797054 | 158834716 |
| HG01106 | hp1 | a0002 | c0002 | t0001 | g0014 | AMR | PUR | MFSD1_chr3_158797054_158834716 | MFSD1 | chr3 | 158797054 | 158834716 |
| HG01106 | hp2 | a0003 | c0003 | t0001 | g0049 | AMR | PUR | MFSD1_chr3_158797054_158834716 | MFSD1 | chr3 | 158797054 | 158834716 |
| HG01109 | hp1 | a0001 | c0001 | t0001 | g0003 | AMR | PUR | MFSD1_chr3_158797054_158834716 | MFSD1 | chr3 | 158797054 | 158834716 |
| HG01109 | hp2 | a0001 | c0001 | t0001 | g0115 | AMR | PUR | MFSD1_chr3_158797054_158834716 | MFSD1 | chr3 | 158797054 | 158834716 |
| HG01167 | hp1 | a0002 | c0002 | t0001 | g0051 | AMR | PUR | MFSD1_chr3_158797054_158834716 | MFSD1 | chr3 | 158797054 | 158834716 |
| HG01167 | hp2 | a0001 | c0001 | t0001 | g0226 | AMR | PUR | MFSD1_chr3_158797054_158834716 | MFSD1 | chr3 | 158797054 | 158834716 |
| HG01168 | hp1 | a0003 | c0003 | t0001 | g0049 | AMR | PUR | MFSD1_chr3_158797054_158834716 | MFSD1 | chr3 | 158797054 | 158834716 |
| HG01168 | hp2 | a0001 | c0001 | t0001 | g0066 | AMR | PUR | MFSD1_chr3_158797054_158834716 | MFSD1 | chr3 | 158797054 | 158834716 |
| HG01175 | hp1 | a0004 | c0005 | t0001 | g0023 | AMR | PUR | MFSD1_chr3_158797054_158834716 | MFSD1 | chr3 | 158797054 | 158834716 |
| HG01175 | hp2 | a0002 | c0004 | t0001 | g0155 | AMR | PUR | MFSD1_chr3_158797054_158834716 | MFSD1 | chr3 | 158797054 | 158834716 |
| HG01192 | hp1 | a0001 | c0001 | t0001 | g0235 | AMR | PUR | MFSD1_chr3_158797054_158834716 | MFSD1 | chr3 | 158797054 | 158834716 |
| HG01192 | hp2 | a0001 | c0001 | t0001 | g0010 | AMR | PUR | MFSD1_chr3_158797054_158834716 | MFSD1 | chr3 | 158797054 | 158834716 |
| HG01243 | hp1 | a0002 | c0002 | t0003 | g0019 | AMR | PUR | MFSD1_chr3_158797054_158834716 | MFSD1 | chr3 | 158797054 | 158834716 |
| HG01243 | hp2 | a0002 | c0002 | t0001 | g0138 | AMR | PUR | MFSD1_chr3_158797054_158834716 | MFSD1 | chr3 | 158797054 | 158834716 |
| HG01255 | hp1 | a0002 | c0002 | t0003 | g0015 | AMR | CLM | MFSD1_chr3_158797054_158834716 | MFSD1 | chr3 | 158797054 | 158834716 |
| HG01255 | hp2 | a0001 | c0001 | t0001 | g0086 | AMR | CLM | MFSD1_chr3_158797054_158834716 | MFSD1 | chr3 | 158797054 | 158834716 |
| HG01256 | hp1 | a0003 | c0003 | t0002 | g0002 | AMR | CLM | MFSD1_chr3_158797054_158834716 | MFSD1 | chr3 | 158797054 | 158834716 |
| HG01256 | hp2 | a0002 | c0004 | t0001 | g0194 | AMR | CLM | MFSD1_chr3_158797054_158834716 | MFSD1 | chr3 | 158797054 | 158834716 |
| HG01257 | hp1 | a0002 | c0002 | t0001 | g0013 | AMR | CLM | MFSD1_chr3_158797054_158834716 | MFSD1 | chr3 | 158797054 | 158834716 |
| HG01257 | hp2 | a0002 | c0002 | t0001 | g0054 | AMR | CLM | MFSD1_chr3_158797054_158834716 | MFSD1 | chr3 | 158797054 | 158834716 |
| HG01258 | hp1 | a0003 | c0003 | t0002 | g0002 | AMR | CLM | MFSD1_chr3_158797054_158834716 | MFSD1 | chr3 | 158797054 | 158834716 |
| HG01258 | hp2 | a0002 | c0002 | t0001 | g0054 | AMR | CLM | MFSD1_chr3_158797054_158834716 | MFSD1 | chr3 | 158797054 | 158834716 |
| HG01261 | hp1 | a0001 | c0001 | t0001 | g0040 | AMR | CLM | MFSD1_chr3_158797054_158834716 | MFSD1 | chr3 | 158797054 | 158834716 |
| HG01261 | hp2 | a0001 | c0007 | t0001 | g0161 | AMR | CLM | MFSD1_chr3_158797054_158834716 | MFSD1 | chr3 | 158797054 | 158834716 |
| HG01346 | hp1 | a0002 | c0002 | t0001 | g0233 | AMR | CLM | MFSD1_chr3_158797054_158834716 | MFSD1 | chr3 | 158797054 | 158834716 |
| HG01346 | hp2 | a0001 | c0001 | t0001 | g0039 | AMR | CLM | MFSD1_chr3_158797054_158834716 | MFSD1 | chr3 | 158797054 | 158834716 |
| HG01358 | hp1 | a0002 | c0002 | t0001 | g0027 | AMR | CLM | MFSD1_chr3_158797054_158834716 | MFSD1 | chr3 | 158797054 | 158834716 |
| HG01358 | hp2 | a0002 | c0002 | t0001 | g0191 | AMR | CLM | MFSD1_chr3_158797054_158834716 | MFSD1 | chr3 | 158797054 | 158834716 |
| HG01361 | hp1 | a0001 | c0001 | t0001 | g0118 | AMR | CLM | MFSD1_chr3_158797054_158834716 | MFSD1 | chr3 | 158797054 | 158834716 |
| HG01361 | hp2 | a0002 | c0002 | t0001 | g0053 | AMR | CLM | MFSD1_chr3_158797054_158834716 | MFSD1 | chr3 | 158797054 | 158834716 |
| HG01433 | hp1 | a0001 | c0001 | t0001 | g0018 | AMR | CLM | MFSD1_chr3_158797054_158834716 | MFSD1 | chr3 | 158797054 | 158834716 |
| HG01433 | hp2 | a0002 | c0002 | t0010 | g0139 | AMR | CLM | MFSD1_chr3_158797054_158834716 | MFSD1 | chr3 | 158797054 | 158834716 |
| HG01496 | hp1 | a0001 | c0001 | t0001 | g0039 | AMR | CLM | MFSD1_chr3_158797054_158834716 | MFSD1 | chr3 | 158797054 | 158834716 |
| HG01496 | hp2 | a0001 | c0001 | t0001 | g0120 | AMR | CLM | MFSD1_chr3_158797054_158834716 | MFSD1 | chr3 | 158797054 | 158834716 |
| HG01515 | hp1 | a0001 | c0001 | t0001 | g0016 | EUR | IBS | MFSD1_chr3_158797054_158834716 | MFSD1 | chr3 | 158797054 | 158834716 |
| HG01515 | hp2 | a0002 | c0002 | t0001 | g0189 | EUR | IBS | MFSD1_chr3_158797054_158834716 | MFSD1 | chr3 | 158797054 | 158834716 |
| HG01517 | hp1 | a0002 | c0002 | t0001 | g0214 | EUR | IBS | MFSD1_chr3_158797054_158834716 | MFSD1 | chr3 | 158797054 | 158834716 |
| HG01517 | hp2 | a0001 | c0001 | t0001 | g0016 | EUR | IBS | MFSD1_chr3_158797054_158834716 | MFSD1 | chr3 | 158797054 | 158834716 |
| HG01884 | hp1 | a0001 | c0001 | t0001 | g0026 | AFR | ACB | MFSD1_chr3_158797054_158834716 | MFSD1 | chr3 | 158797054 | 158834716 |
| HG01884 | hp2 | a0002 | c0002 | t0001 | g0017 | AFR | ACB | MFSD1_chr3_158797054_158834716 | MFSD1 | chr3 | 158797054 | 158834716 |
| HG01891 | hp1 | a0002 | c0002 | t0003 | g0020 | AFR | ACB | MFSD1_chr3_158797054_158834716 | MFSD1 | chr3 | 158797054 | 158834716 |
| HG01891 | hp2 | a0002 | c0002 | t0001 | g0218 | AFR | ACB | MFSD1_chr3_158797054_158834716 | MFSD1 | chr3 | 158797054 | 158834716 |
| HG01934 | hp1 | a0002 | c0004 | t0001 | g0149 | AMR | PEL | MFSD1_chr3_158797054_158834716 | MFSD1 | chr3 | 158797054 | 158834716 |
| HG01934 | hp2 | a0001 | c0001 | t0001 | g0018 | AMR | PEL | MFSD1_chr3_158797054_158834716 | MFSD1 | chr3 | 158797054 | 158834716 |
| HG01952 | hp1 | a0001 | c0001 | t0001 | g0012 | AMR | PEL | MFSD1_chr3_158797054_158834716 | MFSD1 | chr3 | 158797054 | 158834716 |
| HG01952 | hp2 | a0001 | c0001 | t0001 | g0003 | AMR | PEL | MFSD1_chr3_158797054_158834716 | MFSD1 | chr3 | 158797054 | 158834716 |
| HG01978 | hp1 | a0002 | c0002 | t0001 | g0229 | AMR | PEL | MFSD1_chr3_158797054_158834716 | MFSD1 | chr3 | 158797054 | 158834716 |
| HG01978 | hp2 | a0001 | c0001 | t0001 | g0109 | AMR | PEL | MFSD1_chr3_158797054_158834716 | MFSD1 | chr3 | 158797054 | 158834716 |
| HG01981 | hp1 | a0001 | c0001 | t0011 | g0106 | AMR | PEL | MFSD1_chr3_158797054_158834716 | MFSD1 | chr3 | 158797054 | 158834716 |
| HG01981 | hp2 | a0001 | c0001 | t0001 | g0007 | AMR | PEL | MFSD1_chr3_158797054_158834716 | MFSD1 | chr3 | 158797054 | 158834716 |
| HG01993 | hp1 | a0002 | c0002 | t0001 | g0227 | AMR | PEL | MFSD1_chr3_158797054_158834716 | MFSD1 | chr3 | 158797054 | 158834716 |
| HG01993 | hp2 | a0001 | c0001 | t0001 | g0112 | AMR | PEL | MFSD1_chr3_158797054_158834716 | MFSD1 | chr3 | 158797054 | 158834716 |
| HG02015 | hp1 | a0002 | c0004 | t0001 | g0001 | EAS | KHV | MFSD1_chr3_158797054_158834716 | MFSD1 | chr3 | 158797054 | 158834716 |
| HG02015 | hp2 | a0001 | c0001 | t0001 | g0036 | EAS | KHV | MFSD1_chr3_158797054_158834716 | MFSD1 | chr3 | 158797054 | 158834716 |
| HG02027 | hp1 | a0002 | c0004 | t0001 | g0085 | EAS | KHV | MFSD1_chr3_158797054_158834716 | MFSD1 | chr3 | 158797054 | 158834716 |
| HG02027 | hp2 | a0002 | c0002 | t0001 | g0008 | EAS | KHV | MFSD1_chr3_158797054_158834716 | MFSD1 | chr3 | 158797054 | 158834716 |
| HG02040 | hp1 | a0002 | c0002 | t0001 | g0153 | EAS | KHV | MFSD1_chr3_158797054_158834716 | MFSD1 | chr3 | 158797054 | 158834716 |
| HG02040 | hp2 | a0001 | c0001 | t0001 | g0070 | EAS | KHV | MFSD1_chr3_158797054_158834716 | MFSD1 | chr3 | 158797054 | 158834716 |
| HG02055 | hp1 | a0002 | c0002 | t0003 | g0020 | AFR | ACB | MFSD1_chr3_158797054_158834716 | MFSD1 | chr3 | 158797054 | 158834716 |
| HG02055 | hp2 | a0002 | c0002 | t0001 | g0057 | AFR | ACB | MFSD1_chr3_158797054_158834716 | MFSD1 | chr3 | 158797054 | 158834716 |
| HG02056 | hp1 | a0001 | c0001 | t0001 | g0131 | EAS | KHV | MFSD1_chr3_158797054_158834716 | MFSD1 | chr3 | 158797054 | 158834716 |
| HG02056 | hp2 | a0003 | c0003 | t0002 | g0002 | EAS | KHV | MFSD1_chr3_158797054_158834716 | MFSD1 | chr3 | 158797054 | 158834716 |
| HG02074 | hp1 | a0001 | c0001 | t0004 | g0091 | EAS | KHV | MFSD1_chr3_158797054_158834716 | MFSD1 | chr3 | 158797054 | 158834716 |
| HG02074 | hp2 | a0001 | c0001 | t0001 | g0095 | EAS | KHV | MFSD1_chr3_158797054_158834716 | MFSD1 | chr3 | 158797054 | 158834716 |
| HG02080 | hp1 | a0002 | c0002 | t0001 | g0009 | EAS | KHV | MFSD1_chr3_158797054_158834716 | MFSD1 | chr3 | 158797054 | 158834716 |
| HG02080 | hp2 | a0003 | c0003 | t0002 | g0004 | EAS | KHV | MFSD1_chr3_158797054_158834716 | MFSD1 | chr3 | 158797054 | 158834716 |
| HG02129 | hp1 | a0002 | c0002 | t0001 | g0013 | EAS | KHV | MFSD1_chr3_158797054_158834716 | MFSD1 | chr3 | 158797054 | 158834716 |
| HG02129 | hp2 | a0005 | c0006 | t0001 | g0179 | EAS | KHV | MFSD1_chr3_158797054_158834716 | MFSD1 | chr3 | 158797054 | 158834716 |
| HG02132 | hp1 | a0001 | c0001 | t0001 | g0121 | EAS | KHV | MFSD1_chr3_158797054_158834716 | MFSD1 | chr3 | 158797054 | 158834716 |
| HG02132 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | KHV | MFSD1_chr3_158797054_158834716 | MFSD1 | chr3 | 158797054 | 158834716 |
| HG02135 | hp1 | a0001 | c0001 | t0009 | g0102 | EAS | KHV | MFSD1_chr3_158797054_158834716 | MFSD1 | chr3 | 158797054 | 158834716 |
| HG02135 | hp2 | a0003 | c0003 | t0002 | g0050 | EAS | KHV | MFSD1_chr3_158797054_158834716 | MFSD1 | chr3 | 158797054 | 158834716 |
| HG02145 | hp1 | a0001 | c0001 | t0001 | g0147 | AFR | ACB | MFSD1_chr3_158797054_158834716 | MFSD1 | chr3 | 158797054 | 158834716 |
| HG02145 | hp2 | a0001 | c0001 | t0001 | g0029 | AFR | ACB | MFSD1_chr3_158797054_158834716 | MFSD1 | chr3 | 158797054 | 158834716 |
| HG02148 | hp1 | a0001 | c0001 | t0001 | g0124 | AMR | PEL | MFSD1_chr3_158797054_158834716 | MFSD1 | chr3 | 158797054 | 158834716 |
| HG02148 | hp2 | a0001 | c0001 | t0001 | g0010 | AMR | PEL | MFSD1_chr3_158797054_158834716 | MFSD1 | chr3 | 158797054 | 158834716 |
| HG02155 | hp1 | a0002 | c0004 | t0001 | g0006 | EAS | CDX | MFSD1_chr3_158797054_158834716 | MFSD1 | chr3 | 158797054 | 158834716 |
| HG02155 | hp2 | a0001 | c0001 | t0001 | g0072 | EAS | CDX | MFSD1_chr3_158797054_158834716 | MFSD1 | chr3 | 158797054 | 158834716 |
| HG02165 | hp1 | a0001 | c0001 | t0001 | g0032 | EAS | CDX | MFSD1_chr3_158797054_158834716 | MFSD1 | chr3 | 158797054 | 158834716 |
| HG02165 | hp2 | a0003 | c0003 | t0002 | g0166 | EAS | CDX | MFSD1_chr3_158797054_158834716 | MFSD1 | chr3 | 158797054 | 158834716 |
| HG02257 | hp1 | a0002 | c0002 | t0001 | g0222 | AFR | ACB | MFSD1_chr3_158797054_158834716 | MFSD1 | chr3 | 158797054 | 158834716 |
| HG02257 | hp2 | a0006 | c0009 | t0003 | g0224 | AFR | ACB | MFSD1_chr3_158797054_158834716 | MFSD1 | chr3 | 158797054 | 158834716 |
| HG02258 | hp1 | a0002 | c0002 | t0001 | g0208 | AFR | ACB | MFSD1_chr3_158797054_158834716 | MFSD1 | chr3 | 158797054 | 158834716 |
| HG02258 | hp2 | a0002 | c0002 | t0001 | g0240 | AFR | ACB | MFSD1_chr3_158797054_158834716 | MFSD1 | chr3 | 158797054 | 158834716 |
| HG02273 | hp1 | a0001 | c0001 | t0001 | g0159 | AMR | PEL | MFSD1_chr3_158797054_158834716 | MFSD1 | chr3 | 158797054 | 158834716 |
| HG02273 | hp2 | a0001 | c0001 | t0001 | g0103 | AMR | PEL | MFSD1_chr3_158797054_158834716 | MFSD1 | chr3 | 158797054 | 158834716 |
| HG02280 | hp1 | a0002 | c0002 | t0001 | g0217 | AFR | ACB | MFSD1_chr3_158797054_158834716 | MFSD1 | chr3 | 158797054 | 158834716 |
| HG02280 | hp2 | a0002 | c0002 | t0003 | g0019 | AFR | ACB | MFSD1_chr3_158797054_158834716 | MFSD1 | chr3 | 158797054 | 158834716 |
| HG02300 | hp1 | a0001 | c0001 | t0001 | g0108 | AMR | PEL | MFSD1_chr3_158797054_158834716 | MFSD1 | chr3 | 158797054 | 158834716 |
| HG02300 | hp2 | a0003 | c0003 | t0002 | g0002 | AMR | PEL | MFSD1_chr3_158797054_158834716 | MFSD1 | chr3 | 158797054 | 158834716 |
| HG02451 | hp1 | a0002 | c0002 | t0003 | g0015 | AFR | ACB | MFSD1_chr3_158797054_158834716 | MFSD1 | chr3 | 158797054 | 158834716 |
| HG02451 | hp2 | a0002 | c0002 | t0001 | g0196 | AFR | ACB | MFSD1_chr3_158797054_158834716 | MFSD1 | chr3 | 158797054 | 158834716 |
| HG02523 | hp1 | a0002 | c0004 | t0001 | g0006 | EAS | KHV | MFSD1_chr3_158797054_158834716 | MFSD1 | chr3 | 158797054 | 158834716 |
| HG02523 | hp2 | a0001 | c0001 | t0001 | g0010 | EAS | KHV | MFSD1_chr3_158797054_158834716 | MFSD1 | chr3 | 158797054 | 158834716 |
| HG02572 | hp1 | a0003 | c0003 | t0001 | g0176 | AFR | GWD | MFSD1_chr3_158797054_158834716 | MFSD1 | chr3 | 158797054 | 158834716 |
| HG02572 | hp2 | a0002 | c0002 | t0001 | g0207 | AFR | GWD | MFSD1_chr3_158797054_158834716 | MFSD1 | chr3 | 158797054 | 158834716 |
| HG02602 | hp1 | a0001 | c0001 | t0008 | g0211 | SAS | PJL | MFSD1_chr3_158797054_158834716 | MFSD1 | chr3 | 158797054 | 158834716 |
| HG02602 | hp2 | a0001 | c0001 | t0001 | g0114 | SAS | PJL | MFSD1_chr3_158797054_158834716 | MFSD1 | chr3 | 158797054 | 158834716 |
| HG02622 | hp1 | a0002 | c0002 | t0005 | g0044 | AFR | GWD | MFSD1_chr3_158797054_158834716 | MFSD1 | chr3 | 158797054 | 158834716 |
| HG02622 | hp2 | a0002 | c0002 | t0003 | g0137 | AFR | GWD | MFSD1_chr3_158797054_158834716 | MFSD1 | chr3 | 158797054 | 158834716 |
| HG02630 | hp1 | a0002 | c0002 | t0001 | g0013 | AFR | GWD | MFSD1_chr3_158797054_158834716 | MFSD1 | chr3 | 158797054 | 158834716 |
| HG02630 | hp2 | a0004 | c0005 | t0001 | g0199 | AFR | GWD | MFSD1_chr3_158797054_158834716 | MFSD1 | chr3 | 158797054 | 158834716 |
| HG02647 | hp1 | a0002 | c0002 | t0001 | g0025 | AFR | GWD | MFSD1_chr3_158797054_158834716 | MFSD1 | chr3 | 158797054 | 158834716 |
| HG02647 | hp2 | a0003 | c0003 | t0001 | g0183 | AFR | GWD | MFSD1_chr3_158797054_158834716 | MFSD1 | chr3 | 158797054 | 158834716 |
| HG02683 | hp1 | a0001 | c0001 | t0001 | g0088 | SAS | PJL | MFSD1_chr3_158797054_158834716 | MFSD1 | chr3 | 158797054 | 158834716 |
| HG02683 | hp2 | a0002 | c0002 | t0001 | g0190 | SAS | PJL | MFSD1_chr3_158797054_158834716 | MFSD1 | chr3 | 158797054 | 158834716 |
| HG02698 | hp1 | a0001 | c0001 | t0001 | g0031 | SAS | PJL | MFSD1_chr3_158797054_158834716 | MFSD1 | chr3 | 158797054 | 158834716 |
| HG02698 | hp2 | a0002 | c0002 | t0001 | g0014 | SAS | PJL | MFSD1_chr3_158797054_158834716 | MFSD1 | chr3 | 158797054 | 158834716 |
| HG02723 | hp1 | a0002 | c0002 | t0002 | g0195 | AFR | GWD | MFSD1_chr3_158797054_158834716 | MFSD1 | chr3 | 158797054 | 158834716 |
| HG02723 | hp2 | a0002 | c0002 | t0003 | g0015 | AFR | GWD | MFSD1_chr3_158797054_158834716 | MFSD1 | chr3 | 158797054 | 158834716 |
| HG02735 | hp1 | a0002 | c0008 | t0001 | g0221 | SAS | PJL | MFSD1_chr3_158797054_158834716 | MFSD1 | chr3 | 158797054 | 158834716 |
| HG02735 | hp2 | a0001 | c0001 | t0001 | g0098 | SAS | PJL | MFSD1_chr3_158797054_158834716 | MFSD1 | chr3 | 158797054 | 158834716 |
| HG02738 | hp1 | a0002 | c0002 | t0001 | g0013 | SAS | PJL | MFSD1_chr3_158797054_158834716 | MFSD1 | chr3 | 158797054 | 158834716 |
| HG02738 | hp2 | a0002 | c0004 | t0001 | g0045 | SAS | PJL | MFSD1_chr3_158797054_158834716 | MFSD1 | chr3 | 158797054 | 158834716 |
| HG02809 | hp1 | a0002 | c0002 | t0001 | g0209 | AFR | GWD | MFSD1_chr3_158797054_158834716 | MFSD1 | chr3 | 158797054 | 158834716 |
| HG02809 | hp2 | a0001 | c0001 | t0001 | g0146 | AFR | GWD | MFSD1_chr3_158797054_158834716 | MFSD1 | chr3 | 158797054 | 158834716 |
| HG02818 | hp1 | a0002 | c0002 | t0001 | g0017 | AFR | GWD | MFSD1_chr3_158797054_158834716 | MFSD1 | chr3 | 158797054 | 158834716 |
| HG02818 | hp2 | a0004 | c0005 | t0001 | g0210 | AFR | GWD | MFSD1_chr3_158797054_158834716 | MFSD1 | chr3 | 158797054 | 158834716 |
| HG02886 | hp1 | a0001 | c0001 | t0001 | g0026 | AFR | GWD | MFSD1_chr3_158797054_158834716 | MFSD1 | chr3 | 158797054 | 158834716 |
| HG02886 | hp2 | a0002 | c0002 | t0001 | g0024 | AFR | GWD | MFSD1_chr3_158797054_158834716 | MFSD1 | chr3 | 158797054 | 158834716 |
| HG02895 | hp1 | a0002 | c0002 | t0003 | g0136 | AFR | GWD | MFSD1_chr3_158797054_158834716 | MFSD1 | chr3 | 158797054 | 158834716 |
| HG02895 | hp2 | a0002 | c0002 | t0001 | g0206 | AFR | GWD | MFSD1_chr3_158797054_158834716 | MFSD1 | chr3 | 158797054 | 158834716 |
| HG02896 | hp1 | a0001 | c0001 | t0001 | g0041 | AFR | GWD | MFSD1_chr3_158797054_158834716 | MFSD1 | chr3 | 158797054 | 158834716 |
| HG02896 | hp2 | a0001 | c0001 | t0001 | g0030 | AFR | GWD | MFSD1_chr3_158797054_158834716 | MFSD1 | chr3 | 158797054 | 158834716 |
| HG02897 | hp1 | a0001 | c0001 | t0001 | g0041 | AFR | GWD | MFSD1_chr3_158797054_158834716 | MFSD1 | chr3 | 158797054 | 158834716 |
| HG02897 | hp2 | a0002 | c0002 | t0001 | g0052 | AFR | GWD | MFSD1_chr3_158797054_158834716 | MFSD1 | chr3 | 158797054 | 158834716 |
| HG02922 | hp1 | a0001 | c0001 | t0001 | g0223 | AFR | ESN | MFSD1_chr3_158797054_158834716 | MFSD1 | chr3 | 158797054 | 158834716 |
| HG02922 | hp2 | a0001 | c0001 | t0001 | g0238 | AFR | ESN | MFSD1_chr3_158797054_158834716 | MFSD1 | chr3 | 158797054 | 158834716 |
| HG02965 | hp1 | a0002 | c0002 | t0001 | g0148 | AFR | ESN | MFSD1_chr3_158797054_158834716 | MFSD1 | chr3 | 158797054 | 158834716 |
| HG02965 | hp2 | a0002 | c0002 | t0003 | g0019 | AFR | ESN | MFSD1_chr3_158797054_158834716 | MFSD1 | chr3 | 158797054 | 158834716 |
| HG02970 | hp1 | a0001 | c0001 | t0001 | g0230 | AFR | ESN | MFSD1_chr3_158797054_158834716 | MFSD1 | chr3 | 158797054 | 158834716 |
| HG02970 | hp2 | a0002 | c0002 | t0001 | g0201 | AFR | ESN | MFSD1_chr3_158797054_158834716 | MFSD1 | chr3 | 158797054 | 158834716 |
| HG02976 | hp1 | a0001 | c0001 | t0001 | g0036 | AFR | ESN | MFSD1_chr3_158797054_158834716 | MFSD1 | chr3 | 158797054 | 158834716 |
| HG02976 | hp2 | a0001 | c0001 | t0001 | g0030 | AFR | ESN | MFSD1_chr3_158797054_158834716 | MFSD1 | chr3 | 158797054 | 158834716 |
| HG03041 | hp1 | a0002 | c0002 | t0003 | g0140 | AFR | GWD | MFSD1_chr3_158797054_158834716 | MFSD1 | chr3 | 158797054 | 158834716 |
| HG03041 | hp2 | a0001 | c0001 | t0001 | g0231 | AFR | GWD | MFSD1_chr3_158797054_158834716 | MFSD1 | chr3 | 158797054 | 158834716 |
| HG03098 | hp1 | a0002 | c0002 | t0005 | g0143 | AFR | MSL | MFSD1_chr3_158797054_158834716 | MFSD1 | chr3 | 158797054 | 158834716 |
| HG03098 | hp2 | a0002 | c0002 | t0003 | g0015 | AFR | MSL | MFSD1_chr3_158797054_158834716 | MFSD1 | chr3 | 158797054 | 158834716 |
| HG03130 | hp1 | a0002 | c0004 | t0001 | g0141 | AFR | ESN | MFSD1_chr3_158797054_158834716 | MFSD1 | chr3 | 158797054 | 158834716 |
| HG03130 | hp2 | a0002 | c0002 | t0001 | g0213 | AFR | ESN | MFSD1_chr3_158797054_158834716 | MFSD1 | chr3 | 158797054 | 158834716 |
| HG03139 | hp1 | a0001 | c0001 | t0001 | g0142 | AFR | ESN | MFSD1_chr3_158797054_158834716 | MFSD1 | chr3 | 158797054 | 158834716 |
| HG03139 | hp2 | a0002 | c0002 | t0001 | g0057 | AFR | ESN | MFSD1_chr3_158797054_158834716 | MFSD1 | chr3 | 158797054 | 158834716 |
| HG03195 | hp1 | a0002 | c0002 | t0001 | g0198 | AFR | ESN | MFSD1_chr3_158797054_158834716 | MFSD1 | chr3 | 158797054 | 158834716 |
| HG03195 | hp2 | a0002 | c0002 | t0001 | g0024 | AFR | ESN | MFSD1_chr3_158797054_158834716 | MFSD1 | chr3 | 158797054 | 158834716 |
| HG03209 | hp1 | a0001 | c0001 | t0001 | g0026 | AFR | MSL | MFSD1_chr3_158797054_158834716 | MFSD1 | chr3 | 158797054 | 158834716 |
| HG03209 | hp2 | a0002 | c0002 | t0001 | g0241 | AFR | MSL | MFSD1_chr3_158797054_158834716 | MFSD1 | chr3 | 158797054 | 158834716 |
| HG03225 | hp1 | a0002 | c0002 | t0001 | g0017 | AFR | MSL | MFSD1_chr3_158797054_158834716 | MFSD1 | chr3 | 158797054 | 158834716 |
| HG03225 | hp2 | a0003 | c0003 | t0002 | g0172 | AFR | MSL | MFSD1_chr3_158797054_158834716 | MFSD1 | chr3 | 158797054 | 158834716 |
| HG03239 | hp1 | a0002 | c0002 | t0001 | g0027 | SAS | PJL | MFSD1_chr3_158797054_158834716 | MFSD1 | chr3 | 158797054 | 158834716 |
| HG03239 | hp2 | a0001 | c0001 | t0001 | g0158 | SAS | PJL | MFSD1_chr3_158797054_158834716 | MFSD1 | chr3 | 158797054 | 158834716 |
| HG03453 | hp1 | a0002 | c0002 | t0001 | g0017 | AFR | MSL | MFSD1_chr3_158797054_158834716 | MFSD1 | chr3 | 158797054 | 158834716 |
| HG03453 | hp2 | a0001 | c0001 | t0001 | g0232 | AFR | MSL | MFSD1_chr3_158797054_158834716 | MFSD1 | chr3 | 158797054 | 158834716 |
| HG03486 | hp1 | a0002 | c0002 | t0001 | g0192 | AFR | MSL | MFSD1_chr3_158797054_158834716 | MFSD1 | chr3 | 158797054 | 158834716 |
| HG03486 | hp2 | a0002 | c0002 | t0001 | g0025 | AFR | MSL | MFSD1_chr3_158797054_158834716 | MFSD1 | chr3 | 158797054 | 158834716 |
| HG03490 | hp1 | a0002 | c0004 | t0001 | g0045 | SAS | PJL | MFSD1_chr3_158797054_158834716 | MFSD1 | chr3 | 158797054 | 158834716 |
| HG03490 | hp2 | a0002 | c0004 | t0001 | g0055 | SAS | PJL | MFSD1_chr3_158797054_158834716 | MFSD1 | chr3 | 158797054 | 158834716 |
| HG03491 | hp1 | a0002 | c0002 | t0001 | g0008 | SAS | PJL | MFSD1_chr3_158797054_158834716 | MFSD1 | chr3 | 158797054 | 158834716 |
| HG03491 | hp2 | a0001 | c0001 | t0001 | g0079 | SAS | PJL | MFSD1_chr3_158797054_158834716 | MFSD1 | chr3 | 158797054 | 158834716 |
| HG03492 | hp1 | a0001 | c0001 | t0001 | g0093 | SAS | PJL | MFSD1_chr3_158797054_158834716 | MFSD1 | chr3 | 158797054 | 158834716 |
| HG03492 | hp2 | a0002 | c0004 | t0001 | g0001 | SAS | PJL | MFSD1_chr3_158797054_158834716 | MFSD1 | chr3 | 158797054 | 158834716 |
| HG03516 | hp1 | a0003 | c0003 | t0002 | g0185 | AFR | ESN | MFSD1_chr3_158797054_158834716 | MFSD1 | chr3 | 158797054 | 158834716 |
| HG03516 | hp2 | a0002 | c0002 | t0001 | g0024 | AFR | ESN | MFSD1_chr3_158797054_158834716 | MFSD1 | chr3 | 158797054 | 158834716 |
| HG03579 | hp1 | a0002 | c0004 | t0001 | g0200 | AFR | MSL | MFSD1_chr3_158797054_158834716 | MFSD1 | chr3 | 158797054 | 158834716 |
| HG03579 | hp2 | a0002 | c0002 | t0003 | g0043 | AFR | MSL | MFSD1_chr3_158797054_158834716 | MFSD1 | chr3 | 158797054 | 158834716 |
| HG03654 | hp1 | a0002 | c0004 | t0001 | g0055 | SAS | PJL | MFSD1_chr3_158797054_158834716 | MFSD1 | chr3 | 158797054 | 158834716 |
| HG03654 | hp2 | a0001 | c0001 | t0007 | g0077 | SAS | PJL | MFSD1_chr3_158797054_158834716 | MFSD1 | chr3 | 158797054 | 158834716 |
| HG03669 | hp1 | a0001 | c0001 | t0001 | g0034 | SAS | PJL | MFSD1_chr3_158797054_158834716 | MFSD1 | chr3 | 158797054 | 158834716 |
| HG03669 | hp2 | a0002 | c0004 | t0001 | g0022 | SAS | PJL | MFSD1_chr3_158797054_158834716 | MFSD1 | chr3 | 158797054 | 158834716 |
| HG03704 | hp1 | a0001 | c0001 | t0001 | g0157 | SAS | PJL | MFSD1_chr3_158797054_158834716 | MFSD1 | chr3 | 158797054 | 158834716 |
| HG03704 | hp2 | a0001 | c0001 | t0001 | g0069 | SAS | PJL | MFSD1_chr3_158797054_158834716 | MFSD1 | chr3 | 158797054 | 158834716 |
| HG03710 | hp1 | a0001 | c0001 | t0001 | g0003 | SAS | PJL | MFSD1_chr3_158797054_158834716 | MFSD1 | chr3 | 158797054 | 158834716 |
| HG03710 | hp2 | a0002 | c0002 | t0001 | g0125 | SAS | PJL | MFSD1_chr3_158797054_158834716 | MFSD1 | chr3 | 158797054 | 158834716 |
| HG03831 | hp1 | a0001 | c0001 | t0001 | g0037 | SAS | BEB | MFSD1_chr3_158797054_158834716 | MFSD1 | chr3 | 158797054 | 158834716 |
| HG03831 | hp2 | a0005 | c0006 | t0001 | g0178 | SAS | BEB | MFSD1_chr3_158797054_158834716 | MFSD1 | chr3 | 158797054 | 158834716 |
| HG03942 | hp1 | a0002 | c0004 | t0001 | g0001 | SAS | BEB | MFSD1_chr3_158797054_158834716 | MFSD1 | chr3 | 158797054 | 158834716 |
| HG03942 | hp2 | a0003 | c0003 | t0002 | g0002 | SAS | BEB | MFSD1_chr3_158797054_158834716 | MFSD1 | chr3 | 158797054 | 158834716 |
| HG04115 | hp1 | a0003 | c0003 | t0002 | g0184 | SAS | STU | MFSD1_chr3_158797054_158834716 | MFSD1 | chr3 | 158797054 | 158834716 |
| HG04115 | hp2 | a0001 | c0001 | t0001 | g0092 | SAS | STU | MFSD1_chr3_158797054_158834716 | MFSD1 | chr3 | 158797054 | 158834716 |
| HG04184 | hp1 | a0001 | c0001 | t0001 | g0028 | SAS | BEB | MFSD1_chr3_158797054_158834716 | MFSD1 | chr3 | 158797054 | 158834716 |
| HG04184 | hp2 | a0002 | c0004 | t0001 | g0001 | SAS | BEB | MFSD1_chr3_158797054_158834716 | MFSD1 | chr3 | 158797054 | 158834716 |
| HG04199 | hp1 | a0002 | c0002 | t0001 | g0188 | SAS | STU | MFSD1_chr3_158797054_158834716 | MFSD1 | chr3 | 158797054 | 158834716 |
| HG04199 | hp2 | a0002 | c0004 | t0001 | g0001 | SAS | STU | MFSD1_chr3_158797054_158834716 | MFSD1 | chr3 | 158797054 | 158834716 |
| HG04204 | hp1 | a0001 | c0001 | t0001 | g0035 | SAS | STU | MFSD1_chr3_158797054_158834716 | MFSD1 | chr3 | 158797054 | 158834716 |
| HG04204 | hp2 | a0001 | c0001 | t0001 | g0234 | SAS | STU | MFSD1_chr3_158797054_158834716 | MFSD1 | chr3 | 158797054 | 158834716 |
| HG04228 | hp1 | a0001 | c0001 | t0001 | g0018 | SAS | STU | MFSD1_chr3_158797054_158834716 | MFSD1 | chr3 | 158797054 | 158834716 |
| HG04228 | hp2 | a0001 | c0001 | t0001 | g0067 | SAS | STU | MFSD1_chr3_158797054_158834716 | MFSD1 | chr3 | 158797054 | 158834716 |
| NA18522 | hp1 | a0002 | c0002 | t0005 | g0044 | AFR | YRI | MFSD1_chr3_158797054_158834716 | MFSD1 | chr3 | 158797054 | 158834716 |
| NA18522 | hp2 | a0001 | c0001 | t0001 | g0030 | AFR | YRI | MFSD1_chr3_158797054_158834716 | MFSD1 | chr3 | 158797054 | 158834716 |
| NA18612 | hp1 | a0001 | c0001 | t0001 | g0075 | EAS | CHB | MFSD1_chr3_158797054_158834716 | MFSD1 | chr3 | 158797054 | 158834716 |
| NA18612 | hp2 | a0003 | c0003 | t0002 | g0050 | EAS | CHB | MFSD1_chr3_158797054_158834716 | MFSD1 | chr3 | 158797054 | 158834716 |
| NA18747 | hp1 | a0001 | c0001 | t0001 | g0059 | EAS | CHB | MFSD1_chr3_158797054_158834716 | MFSD1 | chr3 | 158797054 | 158834716 |
| NA18747 | hp2 | a0001 | c0001 | t0004 | g0063 | EAS | CHB | MFSD1_chr3_158797054_158834716 | MFSD1 | chr3 | 158797054 | 158834716 |
| NA18906 | hp1 | a0002 | c0004 | t0001 | g0001 | AFR | YRI | MFSD1_chr3_158797054_158834716 | MFSD1 | chr3 | 158797054 | 158834716 |
| NA18906 | hp2 | a0002 | c0002 | t0003 | g0043 | AFR | YRI | MFSD1_chr3_158797054_158834716 | MFSD1 | chr3 | 158797054 | 158834716 |
| NA18939 | hp1 | a0002 | c0004 | t0001 | g0046 | EAS | JPT | MFSD1_chr3_158797054_158834716 | MFSD1 | chr3 | 158797054 | 158834716 |
| NA18939 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | MFSD1_chr3_158797054_158834716 | MFSD1 | chr3 | 158797054 | 158834716 |
| NA18941 | hp1 | a0001 | c0001 | t0001 | g0080 | EAS | JPT | MFSD1_chr3_158797054_158834716 | MFSD1 | chr3 | 158797054 | 158834716 |
| NA18941 | hp2 | a0003 | c0003 | t0002 | g0167 | EAS | JPT | MFSD1_chr3_158797054_158834716 | MFSD1 | chr3 | 158797054 | 158834716 |
| NA18943 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | MFSD1_chr3_158797054_158834716 | MFSD1 | chr3 | 158797054 | 158834716 |
| NA18943 | hp2 | a0002 | c0004 | t0001 | g0001 | EAS | JPT | MFSD1_chr3_158797054_158834716 | MFSD1 | chr3 | 158797054 | 158834716 |
| NA18948 | hp1 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | MFSD1_chr3_158797054_158834716 | MFSD1 | chr3 | 158797054 | 158834716 |
| NA18948 | hp2 | a0001 | c0001 | t0001 | g0104 | EAS | JPT | MFSD1_chr3_158797054_158834716 | MFSD1 | chr3 | 158797054 | 158834716 |
| NA18949 | hp1 | a0002 | c0004 | t0001 | g0001 | EAS | JPT | MFSD1_chr3_158797054_158834716 | MFSD1 | chr3 | 158797054 | 158834716 |
| NA18949 | hp2 | a0001 | c0001 | t0001 | g0032 | EAS | JPT | MFSD1_chr3_158797054_158834716 | MFSD1 | chr3 | 158797054 | 158834716 |
| NA18951 | hp1 | a0003 | c0003 | t0002 | g0004 | EAS | JPT | MFSD1_chr3_158797054_158834716 | MFSD1 | chr3 | 158797054 | 158834716 |
| NA18951 | hp2 | a0001 | c0001 | t0001 | g0089 | EAS | JPT | MFSD1_chr3_158797054_158834716 | MFSD1 | chr3 | 158797054 | 158834716 |
| NA18953 | hp1 | a0001 | c0001 | t0001 | g0087 | EAS | JPT | MFSD1_chr3_158797054_158834716 | MFSD1 | chr3 | 158797054 | 158834716 |
| NA18953 | hp2 | a0003 | c0003 | t0002 | g0002 | EAS | JPT | MFSD1_chr3_158797054_158834716 | MFSD1 | chr3 | 158797054 | 158834716 |
| NA18954 | hp1 | a0003 | c0003 | t0002 | g0168 | EAS | JPT | MFSD1_chr3_158797054_158834716 | MFSD1 | chr3 | 158797054 | 158834716 |
| NA18954 | hp2 | a0003 | c0003 | t0002 | g0002 | EAS | JPT | MFSD1_chr3_158797054_158834716 | MFSD1 | chr3 | 158797054 | 158834716 |
| NA18957 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | MFSD1_chr3_158797054_158834716 | MFSD1 | chr3 | 158797054 | 158834716 |
| NA18957 | hp2 | a0001 | c0001 | t0001 | g0151 | EAS | JPT | MFSD1_chr3_158797054_158834716 | MFSD1 | chr3 | 158797054 | 158834716 |
| NA18960 | hp1 | a0001 | c0001 | t0001 | g0078 | EAS | JPT | MFSD1_chr3_158797054_158834716 | MFSD1 | chr3 | 158797054 | 158834716 |
| NA18960 | hp2 | a0001 | c0001 | t0001 | g0083 | EAS | JPT | MFSD1_chr3_158797054_158834716 | MFSD1 | chr3 | 158797054 | 158834716 |
| NA18962 | hp1 | a0003 | c0003 | t0002 | g0002 | EAS | JPT | MFSD1_chr3_158797054_158834716 | MFSD1 | chr3 | 158797054 | 158834716 |
| NA18962 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | MFSD1_chr3_158797054_158834716 | MFSD1 | chr3 | 158797054 | 158834716 |
| NA18964 | hp1 | a0001 | c0001 | t0001 | g0130 | EAS | JPT | MFSD1_chr3_158797054_158834716 | MFSD1 | chr3 | 158797054 | 158834716 |
| NA18964 | hp2 | a0002 | c0004 | t0001 | g0006 | EAS | JPT | MFSD1_chr3_158797054_158834716 | MFSD1 | chr3 | 158797054 | 158834716 |
| NA18966 | hp1 | a0003 | c0003 | t0002 | g0004 | EAS | JPT | MFSD1_chr3_158797054_158834716 | MFSD1 | chr3 | 158797054 | 158834716 |
| NA18966 | hp2 | a0001 | c0001 | t0001 | g0060 | EAS | JPT | MFSD1_chr3_158797054_158834716 | MFSD1 | chr3 | 158797054 | 158834716 |
| NA18967 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | MFSD1_chr3_158797054_158834716 | MFSD1 | chr3 | 158797054 | 158834716 |
| NA18967 | hp2 | a0002 | c0002 | t0001 | g0009 | EAS | JPT | MFSD1_chr3_158797054_158834716 | MFSD1 | chr3 | 158797054 | 158834716 |
| NA18968 | hp1 | a0001 | c0001 | t0001 | g0042 | EAS | JPT | MFSD1_chr3_158797054_158834716 | MFSD1 | chr3 | 158797054 | 158834716 |
| NA18968 | hp2 | a0002 | c0004 | t0001 | g0001 | EAS | JPT | MFSD1_chr3_158797054_158834716 | MFSD1 | chr3 | 158797054 | 158834716 |
| NA18969 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | MFSD1_chr3_158797054_158834716 | MFSD1 | chr3 | 158797054 | 158834716 |
| NA18969 | hp2 | a0003 | c0003 | t0002 | g0002 | EAS | JPT | MFSD1_chr3_158797054_158834716 | MFSD1 | chr3 | 158797054 | 158834716 |
| NA18970 | hp1 | a0002 | c0004 | t0001 | g0082 | EAS | JPT | MFSD1_chr3_158797054_158834716 | MFSD1 | chr3 | 158797054 | 158834716 |
| NA18970 | hp2 | a0007 | c0011 | t0013 | g0004 | EAS | JPT | MFSD1_chr3_158797054_158834716 | MFSD1 | chr3 | 158797054 | 158834716 |
| NA18971 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | MFSD1_chr3_158797054_158834716 | MFSD1 | chr3 | 158797054 | 158834716 |
| NA18971 | hp2 | a0003 | c0003 | t0002 | g0004 | EAS | JPT | MFSD1_chr3_158797054_158834716 | MFSD1 | chr3 | 158797054 | 158834716 |
| NA18972 | hp1 | a0002 | c0002 | t0001 | g0008 | EAS | JPT | MFSD1_chr3_158797054_158834716 | MFSD1 | chr3 | 158797054 | 158834716 |
| NA18972 | hp2 | a0001 | c0001 | t0001 | g0105 | EAS | JPT | MFSD1_chr3_158797054_158834716 | MFSD1 | chr3 | 158797054 | 158834716 |
| NA18974 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | MFSD1_chr3_158797054_158834716 | MFSD1 | chr3 | 158797054 | 158834716 |
| NA18974 | hp2 | a0003 | c0003 | t0002 | g0004 | EAS | JPT | MFSD1_chr3_158797054_158834716 | MFSD1 | chr3 | 158797054 | 158834716 |
| NA18975 | hp1 | a0001 | c0001 | t0001 | g0101 | EAS | JPT | MFSD1_chr3_158797054_158834716 | MFSD1 | chr3 | 158797054 | 158834716 |
| NA18975 | hp2 | a0002 | c0004 | t0001 | g0163 | EAS | JPT | MFSD1_chr3_158797054_158834716 | MFSD1 | chr3 | 158797054 | 158834716 |
| NA18977 | hp1 | a0001 | c0001 | t0012 | g0084 | EAS | JPT | MFSD1_chr3_158797054_158834716 | MFSD1 | chr3 | 158797054 | 158834716 |
| NA18977 | hp2 | a0002 | c0002 | t0001 | g0008 | EAS | JPT | MFSD1_chr3_158797054_158834716 | MFSD1 | chr3 | 158797054 | 158834716 |
| NA18979 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | MFSD1_chr3_158797054_158834716 | MFSD1 | chr3 | 158797054 | 158834716 |
| NA18979 | hp2 | a0003 | c0003 | t0002 | g0175 | EAS | JPT | MFSD1_chr3_158797054_158834716 | MFSD1 | chr3 | 158797054 | 158834716 |
| NA18982 | hp1 | a0002 | c0002 | t0001 | g0009 | EAS | JPT | MFSD1_chr3_158797054_158834716 | MFSD1 | chr3 | 158797054 | 158834716 |
| NA18982 | hp2 | a0002 | c0004 | t0001 | g0001 | EAS | JPT | MFSD1_chr3_158797054_158834716 | MFSD1 | chr3 | 158797054 | 158834716 |
| NA18983 | hp1 | a0001 | c0001 | t0001 | g0135 | EAS | JPT | MFSD1_chr3_158797054_158834716 | MFSD1 | chr3 | 158797054 | 158834716 |
| NA18983 | hp2 | a0001 | c0001 | t0001 | g0097 | EAS | JPT | MFSD1_chr3_158797054_158834716 | MFSD1 | chr3 | 158797054 | 158834716 |
| NA18984 | hp1 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | MFSD1_chr3_158797054_158834716 | MFSD1 | chr3 | 158797054 | 158834716 |
| NA18984 | hp2 | a0003 | c0003 | t0002 | g0169 | EAS | JPT | MFSD1_chr3_158797054_158834716 | MFSD1 | chr3 | 158797054 | 158834716 |
| NA18985 | hp1 | a0002 | c0004 | t0001 | g0033 | EAS | JPT | MFSD1_chr3_158797054_158834716 | MFSD1 | chr3 | 158797054 | 158834716 |
| NA18985 | hp2 | a0003 | c0003 | t0002 | g0174 | EAS | JPT | MFSD1_chr3_158797054_158834716 | MFSD1 | chr3 | 158797054 | 158834716 |
| NA18986 | hp1 | a0002 | c0004 | t0001 | g0006 | EAS | JPT | MFSD1_chr3_158797054_158834716 | MFSD1 | chr3 | 158797054 | 158834716 |
| NA18986 | hp2 | a0001 | c0001 | t0001 | g0134 | EAS | JPT | MFSD1_chr3_158797054_158834716 | MFSD1 | chr3 | 158797054 | 158834716 |
| NA18988 | hp1 | a0002 | c0004 | t0001 | g0001 | EAS | JPT | MFSD1_chr3_158797054_158834716 | MFSD1 | chr3 | 158797054 | 158834716 |
| NA18988 | hp2 | a0001 | c0001 | t0001 | g0071 | EAS | JPT | MFSD1_chr3_158797054_158834716 | MFSD1 | chr3 | 158797054 | 158834716 |
| NA18989 | hp1 | a0001 | c0001 | t0001 | g0123 | EAS | JPT | MFSD1_chr3_158797054_158834716 | MFSD1 | chr3 | 158797054 | 158834716 |
| NA18989 | hp2 | a0003 | c0003 | t0002 | g0047 | EAS | JPT | MFSD1_chr3_158797054_158834716 | MFSD1 | chr3 | 158797054 | 158834716 |
| NA18990 | hp1 | a0003 | c0003 | t0002 | g0004 | EAS | JPT | MFSD1_chr3_158797054_158834716 | MFSD1 | chr3 | 158797054 | 158834716 |
| NA18990 | hp2 | a0001 | c0001 | t0001 | g0065 | EAS | JPT | MFSD1_chr3_158797054_158834716 | MFSD1 | chr3 | 158797054 | 158834716 |
| NA18992 | hp1 | a0002 | c0004 | t0001 | g0001 | EAS | JPT | MFSD1_chr3_158797054_158834716 | MFSD1 | chr3 | 158797054 | 158834716 |
| NA18992 | hp2 | a0003 | c0003 | t0002 | g0177 | EAS | JPT | MFSD1_chr3_158797054_158834716 | MFSD1 | chr3 | 158797054 | 158834716 |
| NA18994 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | MFSD1_chr3_158797054_158834716 | MFSD1 | chr3 | 158797054 | 158834716 |
| NA18994 | hp2 | a0001 | c0001 | t0001 | g0064 | EAS | JPT | MFSD1_chr3_158797054_158834716 | MFSD1 | chr3 | 158797054 | 158834716 |
| NA18998 | hp1 | a0001 | c0001 | t0001 | g0035 | EAS | JPT | MFSD1_chr3_158797054_158834716 | MFSD1 | chr3 | 158797054 | 158834716 |
| NA18998 | hp2 | a0002 | c0004 | t0001 | g0001 | EAS | JPT | MFSD1_chr3_158797054_158834716 | MFSD1 | chr3 | 158797054 | 158834716 |
| NA18999 | hp1 | a0002 | c0002 | t0001 | g0009 | EAS | JPT | MFSD1_chr3_158797054_158834716 | MFSD1 | chr3 | 158797054 | 158834716 |
| NA18999 | hp2 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | MFSD1_chr3_158797054_158834716 | MFSD1 | chr3 | 158797054 | 158834716 |
| NA19000 | hp1 | a0002 | c0004 | t0001 | g0001 | EAS | JPT | MFSD1_chr3_158797054_158834716 | MFSD1 | chr3 | 158797054 | 158834716 |
| NA19000 | hp2 | a0001 | c0001 | t0001 | g0068 | EAS | JPT | MFSD1_chr3_158797054_158834716 | MFSD1 | chr3 | 158797054 | 158834716 |
| NA19003 | hp1 | a0002 | c0002 | t0001 | g0008 | EAS | JPT | MFSD1_chr3_158797054_158834716 | MFSD1 | chr3 | 158797054 | 158834716 |
| NA19003 | hp2 | a0001 | c0001 | t0001 | g0090 | EAS | JPT | MFSD1_chr3_158797054_158834716 | MFSD1 | chr3 | 158797054 | 158834716 |
| NA19006 | hp1 | a0002 | c0004 | t0001 | g0154 | EAS | JPT | MFSD1_chr3_158797054_158834716 | MFSD1 | chr3 | 158797054 | 158834716 |
| NA19006 | hp2 | a0001 | c0001 | t0001 | g0117 | EAS | JPT | MFSD1_chr3_158797054_158834716 | MFSD1 | chr3 | 158797054 | 158834716 |
| NA19007 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | MFSD1_chr3_158797054_158834716 | MFSD1 | chr3 | 158797054 | 158834716 |
| NA19007 | hp2 | a0003 | c0003 | t0002 | g0004 | EAS | JPT | MFSD1_chr3_158797054_158834716 | MFSD1 | chr3 | 158797054 | 158834716 |
| NA19009 | hp1 | a0001 | c0001 | t0001 | g0096 | EAS | JPT | MFSD1_chr3_158797054_158834716 | MFSD1 | chr3 | 158797054 | 158834716 |
| NA19009 | hp2 | a0003 | c0003 | t0002 | g0002 | EAS | JPT | MFSD1_chr3_158797054_158834716 | MFSD1 | chr3 | 158797054 | 158834716 |
| NA19010 | hp1 | a0002 | c0004 | t0001 | g0001 | EAS | JPT | MFSD1_chr3_158797054_158834716 | MFSD1 | chr3 | 158797054 | 158834716 |
| NA19010 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | MFSD1_chr3_158797054_158834716 | MFSD1 | chr3 | 158797054 | 158834716 |
| NA19011 | hp1 | a0003 | c0003 | t0002 | g0002 | EAS | JPT | MFSD1_chr3_158797054_158834716 | MFSD1 | chr3 | 158797054 | 158834716 |
| NA19011 | hp2 | a0001 | c0001 | t0001 | g0132 | EAS | JPT | MFSD1_chr3_158797054_158834716 | MFSD1 | chr3 | 158797054 | 158834716 |
| NA19012 | hp1 | a0002 | c0004 | t0001 | g0144 | EAS | JPT | MFSD1_chr3_158797054_158834716 | MFSD1 | chr3 | 158797054 | 158834716 |
| NA19012 | hp2 | a0001 | c0001 | t0001 | g0038 | EAS | JPT | MFSD1_chr3_158797054_158834716 | MFSD1 | chr3 | 158797054 | 158834716 |
| NA19030 | hp1 | a0001 | c0001 | t0001 | g0056 | AFR | LWK | MFSD1_chr3_158797054_158834716 | MFSD1 | chr3 | 158797054 | 158834716 |
| NA19030 | hp2 | a0001 | c0001 | t0001 | g0237 | AFR | LWK | MFSD1_chr3_158797054_158834716 | MFSD1 | chr3 | 158797054 | 158834716 |
| NA19043 | hp1 | a0002 | c0002 | t0001 | g0212 | AFR | LWK | MFSD1_chr3_158797054_158834716 | MFSD1 | chr3 | 158797054 | 158834716 |
| NA19043 | hp2 | a0004 | c0005 | t0001 | g0023 | AFR | LWK | MFSD1_chr3_158797054_158834716 | MFSD1 | chr3 | 158797054 | 158834716 |
| NA19054 | hp1 | a0003 | c0003 | t0002 | g0004 | EAS | JPT | MFSD1_chr3_158797054_158834716 | MFSD1 | chr3 | 158797054 | 158834716 |
| NA19054 | hp2 | a0001 | c0001 | t0004 | g0110 | EAS | JPT | MFSD1_chr3_158797054_158834716 | MFSD1 | chr3 | 158797054 | 158834716 |
| NA19056 | hp1 | a0001 | c0001 | t0001 | g0122 | EAS | JPT | MFSD1_chr3_158797054_158834716 | MFSD1 | chr3 | 158797054 | 158834716 |
| NA19056 | hp2 | a0003 | c0003 | t0002 | g0171 | EAS | JPT | MFSD1_chr3_158797054_158834716 | MFSD1 | chr3 | 158797054 | 158834716 |
| NA19057 | hp1 | a0003 | c0003 | t0002 | g0180 | EAS | JPT | MFSD1_chr3_158797054_158834716 | MFSD1 | chr3 | 158797054 | 158834716 |
| NA19057 | hp2 | a0001 | c0001 | t0001 | g0099 | EAS | JPT | MFSD1_chr3_158797054_158834716 | MFSD1 | chr3 | 158797054 | 158834716 |
| NA19058 | hp1 | a0002 | c0002 | t0001 | g0009 | EAS | JPT | MFSD1_chr3_158797054_158834716 | MFSD1 | chr3 | 158797054 | 158834716 |
| NA19058 | hp2 | a0003 | c0003 | t0002 | g0002 | EAS | JPT | MFSD1_chr3_158797054_158834716 | MFSD1 | chr3 | 158797054 | 158834716 |
| NA19060 | hp1 | a0001 | c0001 | t0001 | g0074 | EAS | JPT | MFSD1_chr3_158797054_158834716 | MFSD1 | chr3 | 158797054 | 158834716 |
| NA19060 | hp2 | a0001 | c0001 | t0001 | g0126 | EAS | JPT | MFSD1_chr3_158797054_158834716 | MFSD1 | chr3 | 158797054 | 158834716 |
| NA19064 | hp1 | a0003 | c0003 | t0002 | g0004 | EAS | JPT | MFSD1_chr3_158797054_158834716 | MFSD1 | chr3 | 158797054 | 158834716 |
| NA19064 | hp2 | a0001 | c0001 | t0001 | g0073 | EAS | JPT | MFSD1_chr3_158797054_158834716 | MFSD1 | chr3 | 158797054 | 158834716 |
| NA19065 | hp1 | a0003 | c0003 | t0002 | g0181 | EAS | JPT | MFSD1_chr3_158797054_158834716 | MFSD1 | chr3 | 158797054 | 158834716 |
| NA19065 | hp2 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | MFSD1_chr3_158797054_158834716 | MFSD1 | chr3 | 158797054 | 158834716 |
| NA19067 | hp1 | a0003 | c0003 | t0002 | g0002 | EAS | JPT | MFSD1_chr3_158797054_158834716 | MFSD1 | chr3 | 158797054 | 158834716 |
| NA19067 | hp2 | a0001 | c0001 | t0001 | g0127 | EAS | JPT | MFSD1_chr3_158797054_158834716 | MFSD1 | chr3 | 158797054 | 158834716 |
| NA19068 | hp1 | a0002 | c0002 | t0001 | g0204 | EAS | JPT | MFSD1_chr3_158797054_158834716 | MFSD1 | chr3 | 158797054 | 158834716 |
| NA19068 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | MFSD1_chr3_158797054_158834716 | MFSD1 | chr3 | 158797054 | 158834716 |
| NA19074 | hp1 | a0001 | c0001 | t0001 | g0031 | EAS | JPT | MFSD1_chr3_158797054_158834716 | MFSD1 | chr3 | 158797054 | 158834716 |
| NA19074 | hp2 | a0002 | c0004 | t0001 | g0001 | EAS | JPT | MFSD1_chr3_158797054_158834716 | MFSD1 | chr3 | 158797054 | 158834716 |
| NA19075 | hp1 | a0002 | c0004 | t0001 | g0033 | EAS | JPT | MFSD1_chr3_158797054_158834716 | MFSD1 | chr3 | 158797054 | 158834716 |
| NA19075 | hp2 | a0003 | c0003 | t0002 | g0002 | EAS | JPT | MFSD1_chr3_158797054_158834716 | MFSD1 | chr3 | 158797054 | 158834716 |
| NA19077 | hp1 | a0001 | c0001 | t0004 | g0038 | EAS | JPT | MFSD1_chr3_158797054_158834716 | MFSD1 | chr3 | 158797054 | 158834716 |
| NA19077 | hp2 | a0003 | c0003 | t0002 | g0048 | EAS | JPT | MFSD1_chr3_158797054_158834716 | MFSD1 | chr3 | 158797054 | 158834716 |
| NA19078 | hp1 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | MFSD1_chr3_158797054_158834716 | MFSD1 | chr3 | 158797054 | 158834716 |
| NA19078 | hp2 | a0002 | c0004 | t0001 | g0165 | EAS | JPT | MFSD1_chr3_158797054_158834716 | MFSD1 | chr3 | 158797054 | 158834716 |
| NA19079 | hp1 | a0002 | c0004 | t0001 | g0150 | EAS | JPT | MFSD1_chr3_158797054_158834716 | MFSD1 | chr3 | 158797054 | 158834716 |
| NA19079 | hp2 | a0003 | c0003 | t0002 | g0002 | EAS | JPT | MFSD1_chr3_158797054_158834716 | MFSD1 | chr3 | 158797054 | 158834716 |
| NA19080 | hp1 | a0003 | c0003 | t0002 | g0173 | EAS | JPT | MFSD1_chr3_158797054_158834716 | MFSD1 | chr3 | 158797054 | 158834716 |
| NA19080 | hp2 | a0001 | c0001 | t0001 | g0094 | EAS | JPT | MFSD1_chr3_158797054_158834716 | MFSD1 | chr3 | 158797054 | 158834716 |
| NA19081 | hp1 | a0001 | c0001 | t0001 | g0111 | EAS | JPT | MFSD1_chr3_158797054_158834716 | MFSD1 | chr3 | 158797054 | 158834716 |
| NA19081 | hp2 | a0002 | c0004 | t0001 | g0046 | EAS | JPT | MFSD1_chr3_158797054_158834716 | MFSD1 | chr3 | 158797054 | 158834716 |
| NA19083 | hp1 | a0003 | c0003 | t0002 | g0002 | EAS | JPT | MFSD1_chr3_158797054_158834716 | MFSD1 | chr3 | 158797054 | 158834716 |
| NA19083 | hp2 | a0001 | c0001 | t0001 | g0100 | EAS | JPT | MFSD1_chr3_158797054_158834716 | MFSD1 | chr3 | 158797054 | 158834716 |
| NA19084 | hp1 | a0001 | c0001 | t0001 | g0037 | EAS | JPT | MFSD1_chr3_158797054_158834716 | MFSD1 | chr3 | 158797054 | 158834716 |
| NA19084 | hp2 | a0003 | c0003 | t0002 | g0002 | EAS | JPT | MFSD1_chr3_158797054_158834716 | MFSD1 | chr3 | 158797054 | 158834716 |
| NA19085 | hp1 | a0002 | c0002 | t0001 | g0128 | EAS | JPT | MFSD1_chr3_158797054_158834716 | MFSD1 | chr3 | 158797054 | 158834716 |
| NA19085 | hp2 | a0001 | c0001 | t0001 | g0076 | EAS | JPT | MFSD1_chr3_158797054_158834716 | MFSD1 | chr3 | 158797054 | 158834716 |
| NA19087 | hp1 | a0001 | c0001 | t0001 | g0034 | EAS | JPT | MFSD1_chr3_158797054_158834716 | MFSD1 | chr3 | 158797054 | 158834716 |
| NA19087 | hp2 | a0002 | c0004 | t0001 | g0001 | EAS | JPT | MFSD1_chr3_158797054_158834716 | MFSD1 | chr3 | 158797054 | 158834716 |
| NA19088 | hp1 | a0003 | c0003 | t0002 | g0047 | EAS | JPT | MFSD1_chr3_158797054_158834716 | MFSD1 | chr3 | 158797054 | 158834716 |
| NA19088 | hp2 | a0001 | c0001 | t0001 | g0107 | EAS | JPT | MFSD1_chr3_158797054_158834716 | MFSD1 | chr3 | 158797054 | 158834716 |
| NA19090 | hp1 | a0002 | c0004 | t0001 | g0001 | EAS | JPT | MFSD1_chr3_158797054_158834716 | MFSD1 | chr3 | 158797054 | 158834716 |
| NA19090 | hp2 | a0003 | c0003 | t0002 | g0182 | EAS | JPT | MFSD1_chr3_158797054_158834716 | MFSD1 | chr3 | 158797054 | 158834716 |
| NA19091 | hp1 | a0002 | c0004 | t0001 | g0164 | EAS | JPT | MFSD1_chr3_158797054_158834716 | MFSD1 | chr3 | 158797054 | 158834716 |
| NA19091 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | MFSD1_chr3_158797054_158834716 | MFSD1 | chr3 | 158797054 | 158834716 |
| NA19240 | hp1 | a0001 | c0001 | t0001 | g0029 | AFR | YRI | MFSD1_chr3_158797054_158834716 | MFSD1 | chr3 | 158797054 | 158834716 |
| NA19240 | hp2 | a0002 | c0002 | t0001 | g0216 | AFR | YRI | MFSD1_chr3_158797054_158834716 | MFSD1 | chr3 | 158797054 | 158834716 |
| NA20129 | hp1 | a0001 | c0001 | t0001 | g0003 | AFR | ASW | MFSD1_chr3_158797054_158834716 | MFSD1 | chr3 | 158797054 | 158834716 |
| NA20129 | hp2 | a0002 | c0002 | t0001 | g0025 | AFR | ASW | MFSD1_chr3_158797054_158834716 | MFSD1 | chr3 | 158797054 | 158834716 |
| NA20805 | hp1 | a0002 | c0004 | t0001 | g0022 | EUR | TSI | MFSD1_chr3_158797054_158834716 | MFSD1 | chr3 | 158797054 | 158834716 |
| NA20805 | hp2 | a0002 | c0004 | t0001 | g0001 | EUR | TSI | MFSD1_chr3_158797054_158834716 | MFSD1 | chr3 | 158797054 | 158834716 |
| NA20905 | hp1 | a0001 | c0001 | t0001 | g0016 | SAS | GIH | MFSD1_chr3_158797054_158834716 | MFSD1 | chr3 | 158797054 | 158834716 |
| NA20905 | hp2 | a0002 | c0002 | t0001 | g0215 | SAS | GIH | MFSD1_chr3_158797054_158834716 | MFSD1 | chr3 | 158797054 | 158834716 |
| HG01123 | hp1 | a0002 | c0004 | t0001 | g0001 | AMR | CLM | MFSD1_chr3_158797054_158834716 | MFSD1 | chr3 | 158797054 | 158834716 |
| HG01123 | hp2 | a0001 | c0001 | t0001 | g0113 | AMR | CLM | MFSD1_chr3_158797054_158834716 | MFSD1 | chr3 | 158797054 | 158834716 |
| HG02109 | hp1 | a0001 | c0001 | t0001 | g0145 | AFR | ACB | MFSD1_chr3_158797054_158834716 | MFSD1 | chr3 | 158797054 | 158834716 |
| HG02109 | hp2 | a0002 | c0002 | t0001 | g0197 | AFR | ACB | MFSD1_chr3_158797054_158834716 | MFSD1 | chr3 | 158797054 | 158834716 |
| HG02486 | hp1 | a0001 | c0001 | t0001 | g0058 | AFR | ACB | MFSD1_chr3_158797054_158834716 | MFSD1 | chr3 | 158797054 | 158834716 |
| HG02486 | hp2 | a0004 | c0005 | t0001 | g0023 | AFR | ACB | MFSD1_chr3_158797054_158834716 | MFSD1 | chr3 | 158797054 | 158834716 |
| HG02559 | hp1 | a0002 | c0004 | t0001 | g0006 | AFR | ACB | MFSD1_chr3_158797054_158834716 | MFSD1 | chr3 | 158797054 | 158834716 |
| HG02559 | hp2 | a0003 | c0003 | t0002 | g0170 | AFR | ACB | MFSD1_chr3_158797054_158834716 | MFSD1 | chr3 | 158797054 | 158834716 |
| HG03471 | hp1 | a0002 | c0002 | t0001 | g0219 | AFR | MSL | MFSD1_chr3_158797054_158834716 | MFSD1 | chr3 | 158797054 | 158834716 |
| HG03471 | hp2 | a0002 | c0002 | t0003 | g0020 | AFR | MSL | MFSD1_chr3_158797054_158834716 | MFSD1 | chr3 | 158797054 | 158834716 |
| HG06807 | hp1 | a0002 | c0002 | t0001 | g0239 | AFR | USA | MFSD1_chr3_158797054_158834716 | MFSD1 | chr3 | 158797054 | 158834716 |
| HG06807 | hp2 | a0001 | c0001 | t0001 | g0029 | AFR | USA | MFSD1_chr3_158797054_158834716 | MFSD1 | chr3 | 158797054 | 158834716 |
| NA18955 | hp1 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | MFSD1_chr3_158797054_158834716 | MFSD1 | chr3 | 158797054 | 158834716 |
| NA18955 | hp2 | a0003 | c0003 | t0002 | g0004 | EAS | JPT | MFSD1_chr3_158797054_158834716 | MFSD1 | chr3 | 158797054 | 158834716 |
| NA20300 | hp1 | a0001 | c0001 | t0001 | g0056 | AFR | USA | MFSD1_chr3_158797054_158834716 | MFSD1 | chr3 | 158797054 | 158834716 |
| NA20300 | hp2 | a0002 | c0004 | t0001 | g0162 | AFR | USA | MFSD1_chr3_158797054_158834716 | MFSD1 | chr3 | 158797054 | 158834716 |
| NA21309 | hp1 | a0002 | c0002 | t0001 | g0014 | AFR | LWK | MFSD1_chr3_158797054_158834716 | MFSD1 | chr3 | 158797054 | 158834716 |
| NA21309 | hp2 | a0008 | c0010 | t0001 | g0225 | AFR | LWK | MFSD1_chr3_158797054_158834716 | MFSD1 | chr3 | 158797054 | 158834716 |
| homoSapiens | chm13v2 | a0002 | c0002 | t0002 | g0133 | REF | REF | MFSD1_chr3_158797054_158834716 | MFSD1 | chr3 | 158797054 | 158834716 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0001 | g0081 | REF | REF | MFSD1_chr3_158797054_158834716 | MFSD1 | chr3 | 158797054 | 158834716 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr3:158802178 | G | T | 1 | a0007 | 1 | NA18970.hp2 | missense_variant | MODERATE | c.26G>T | p.Arg9Leu | MFSD1 | ENSG00000118855.21 | transcript | ENST00000415822.8 | protein_coding | 1/16 | 125/2231 | 26/1398 | 9/465 | chr3 | 158802178 | |||
| chr3:158802222 | C | T | 3 | a0003 a0005 a0007 |
64 | HG00280.hp1 HG00423.hp2 HG00609.hp2 others(61): Show |
missense_variant | MODERATE | c.70C>T | p.Pro24Ser | MFSD1 | ENSG00000118855.21 | transcript | ENST00000415822.8 | protein_coding | 1/16 | 169/2231 | 70/1398 | 24/465 | chr3 | 158802222 | |||
| chr3:158805381 | C | T | 1 | a0008 | 1 | NA21309.hp2 | missense_variant | MODERATE | c.236C>T | p.Thr79Met | MFSD1 | ENSG00000118855.21 | transcript | ENST00000415822.8 | protein_coding | 3/16 | 335/2231 | 236/1398 | 79/465 | chr3 | 158805381 | |||
| chr3:158814014 | A | C | 1 | a0004 | 5 | HG01175.hp1 HG02486.hp2 HG02630.hp2 others(2): Show |
missense_variant | MODERATE | c.599A>C | p.Glu200Ala | MFSD1 | ENSG00000118855.21 | transcript | ENST00000415822.8 | protein_coding | 7/16 | 698/2231 | 599/1398 | 200/465 | chr3 | 158814014 | |||
| chr3:158819654 | A | G | 5 | a0002 a0003 a0004 others(2): Show |
224 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(221): Show |
missense_variant | MODERATE | c.658A>G | p.Ile220Val | MFSD1 | ENSG00000118855.21 | transcript | ENST00000415822.8 | protein_coding | 8/16 | 757/2231 | 658/1398 | 220/465 | chr3 | 158819654 | |||
| chr3:158823525 | T | C | 1 | a0006 | 1 | HG02257.hp2 | missense_variant&splice_region_variant | MODERATE | c.1175T>C | p.Phe392Ser | MFSD1 | ENSG00000118855.21 | transcript | ENST00000415822.8 | protein_coding | 12/16 | 1274/2231 | 1175/1398 | 392/465 | chr3 | 158823525 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr3:158820267 | T | C | 2 | a0001c0007 a0002c0004 |
56 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(53): Show |
synonymous_variant | LOW | c.804T>C | p.Leu268Leu | MFSD1 | ENSG00000118855.21 | transcript | ENST00000415822.8 | protein_coding | 9/16 | 903/2231 | 804/1398 | 268/465 | chr3 | 158820267 | |||
| chr3:158822017 | G | A | 1 | a0002c0008 | 1 | HG02735.hp1 | synonymous_variant | LOW | c.954G>A | p.Pro318Pro | MFSD1 | ENSG00000118855.21 | transcript | ENST00000415822.8 | protein_coding | 11/16 | 1053/2231 | 954/1398 | 318/465 | chr3 | 158822017 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr3:158802066 | G | A | 1 | a0001c0001t0004 | 4 | HG02074.hp1 NA18747.hp2 NA19054.hp2 others(1): Show |
5_prime_UTR_variant | MODIFIER | c.-87G>A | MFSD1 | ENSG00000118855.21 | transcript | ENST00000415822.8 | protein_coding | 1/16 | 87 | chr3 | 158802066 | ||||||
| chr3:158802072 | T | G | 1 | a0002c0002t0005 | 3 | HG02622.hp1 HG03098.hp1 NA18522.hp1 |
5_prime_UTR_variant | MODIFIER | c.-81T>G | MFSD1 | ENSG00000118855.21 | transcript | ENST00000415822.8 | protein_coding | 1/16 | 81 | chr3 | 158802072 | ||||||
| chr3:158829048 | T | A | 1 | a0001c0001t0006 | 1 | HG00408.hp1 | 3_prime_UTR_variant | MODIFIER | c.*66T>A | MFSD1 | ENSG00000118855.21 | transcript | ENST00000415822.8 | protein_coding | 16/16 | 66 | chr3 | 158829048 | ||||||
| chr3:158829060 | G | GT | 3 | a0002c0002t0002 a0003c0003t0002 a0007c0011t0013 |
59 | HG00280.hp1 HG00423.hp2 HG00609.hp2 others(56): Show |
3_prime_UTR_variant | MODIFIER | c.*81dupT | MFSD1 | ENSG00000118855.21 | transcript | ENST00000415822.8 | protein_coding | 16/16 | 82 | INFO_REALIGN_3_PRIME | chr3 | 158829060 | |||||
| chr3:158829106 | C | CCAAATAT others(389): Show |
1 | a0001c0001t0012 | 1 | NA18977.hp1 | 3_prime_UTR_variant | MODIFIER | c.*140_*141insTTTTTT others(390): Show |
MFSD1 | ENSG00000118855.21 | transcript | ENST00000415822.8 | protein_coding | 16/16 | 141 | INFO_REALIGN_3_PRIME | chr3 | 158829106 | |||||
| chr3:158829138 | GGCCTGTT others(3): Show |
G | 1 | a0001c0001t0007 | 1 | HG03654.hp2 | 3_prime_UTR_variant | MODIFIER | c.*163_*172delTTTAGC others(4): Show |
MFSD1 | ENSG00000118855.21 | transcript | ENST00000415822.8 | protein_coding | 16/16 | 163 | INFO_REALIGN_3_PRIME | chr3 | 158829138 | |||||
| chr3:158829195 | T | G | 3 | a0002c0002t0002 a0003c0003t0002 a0007c0011t0013 |
59 | HG00280.hp1 HG00423.hp2 HG00609.hp2 others(56): Show |
3_prime_UTR_variant | MODIFIER | c.*213T>G | MFSD1 | ENSG00000118855.21 | transcript | ENST00000415822.8 | protein_coding | 16/16 | 213 | chr3 | 158829195 | ||||||
| chr3:158829237 | C | T | 1 | a0001c0001t0011 | 1 | HG01981.hp1 | 3_prime_UTR_variant | MODIFIER | c.*255C>T | MFSD1 | ENSG00000118855.21 | transcript | ENST00000415822.8 | protein_coding | 16/16 | 255 | chr3 | 158829237 | ||||||
| chr3:158829292 | T | C | 3 | a0002c0002t0003 a0002c0002t0005 a0006c0009t0003 |
19 | HG01243.hp1 HG01255.hp1 HG01891.hp1 others(16): Show |
3_prime_UTR_variant | MODIFIER | c.*310T>C | MFSD1 | ENSG00000118855.21 | transcript | ENST00000415822.8 | protein_coding | 16/16 | 310 | chr3 | 158829292 | ||||||
| chr3:158829423 | C | T | 1 | a0007c0011t0013 | 1 | NA18970.hp2 | 3_prime_UTR_variant | MODIFIER | c.*441C>T | MFSD1 | ENSG00000118855.21 | transcript | ENST00000415822.8 | protein_coding | 16/16 | 441 | chr3 | 158829423 | ||||||
| chr3:158829647 | A | C | 1 | a0002c0002t0010 | 1 | HG01433.hp2 | 3_prime_UTR_variant | MODIFIER | c.*665A>C | MFSD1 | ENSG00000118855.21 | transcript | ENST00000415822.8 | protein_coding | 16/16 | 665 | chr3 | 158829647 | ||||||
| chr3:158829661 | C | T | 1 | a0001c0001t0009 | 1 | HG02135.hp1 | 3_prime_UTR_variant | MODIFIER | c.*679C>T | MFSD1 | ENSG00000118855.21 | transcript | ENST00000415822.8 | protein_coding | 16/16 | 679 | chr3 | 158829661 | ||||||
| chr3:158829713 | C | T | 1 | a0001c0001t0008 | 1 | HG02602.hp1 | 3_prime_UTR_variant | MODIFIER | c.*731C>T | MFSD1 | ENSG00000118855.21 | transcript | ENST00000415822.8 | protein_coding | 16/16 | 731 | chr3 | 158829713 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr3:158802449 | T | C | 1 | a0001c0001t0001g0058 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.163+134T>C | MFSD1 | ENSG00000118855.21 | transcript | ENST00000415822.8 | protein_coding | 1/15 | chr3 | 158802449 | |||||||
| chr3:158802694 | A | G | 145 | a0001c0001t0001g0016 a0001c0001t0001g0026 a0001c0001t0001g0028 others(142): Show |
255 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(252): Show |
intron_variant | MODIFIER | c.163+379A>G | MFSD1 | ENSG00000118855.21 | transcript | ENST00000415822.8 | protein_coding | 1/15 | chr3 | 158802694 | |||||||
| chr3:158802805 | A | G | 3 | a0002c0002t0001g0017 a0002c0002t0001g0240 a0002c0002t0001g0241 |
6 | HG01884.hp2 HG02258.hp2 HG02818.hp1 others(3): Show |
intron_variant | MODIFIER | c.163+490A>G | MFSD1 | ENSG00000118855.21 | transcript | ENST00000415822.8 | protein_coding | 1/15 | chr3 | 158802805 | |||||||
| chr3:158802948 | C | T | 1 | a0002c0002t0001g0239 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.163+633C>T | MFSD1 | ENSG00000118855.21 | transcript | ENST00000415822.8 | protein_coding | 1/15 | chr3 | 158802948 | |||||||
| chr3:158803124 | C | T | 2 | a0001c0001t0001g0134 a0001c0001t0001g0135 |
2 | NA18983.hp1 NA18986.hp2 |
intron_variant | MODIFIER | c.163+809C>T | MFSD1 | ENSG00000118855.21 | transcript | ENST00000415822.8 | protein_coding | 1/15 | chr3 | 158803124 | |||||||
| chr3:158803289 | T | G | 71 | a0001c0001t0001g0142 a0001c0001t0001g0145 a0001c0001t0001g0146 others(68): Show |
138 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(135): Show |
intron_variant | MODIFIER | c.163+974T>G | MFSD1 | ENSG00000118855.21 | transcript | ENST00000415822.8 | protein_coding | 1/15 | chr3 | 158803289 | |||||||
| chr3:158803429 | A | C | 62 | a0001c0001t0001g0142 a0001c0001t0001g0145 a0001c0001t0001g0146 others(59): Show |
124 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(121): Show |
intron_variant | MODIFIER | c.164-890A>C | MFSD1 | ENSG00000118855.21 | transcript | ENST00000415822.8 | protein_coding | 1/15 | chr3 | 158803429 | |||||||
| chr3:158803686 | T | A | 3 | a0001c0001t0001g0142 a0002c0002t0005g0044 a0002c0002t0005g0143 |
4 | HG02622.hp1 HG03098.hp1 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.164-633T>A | MFSD1 | ENSG00000118855.21 | transcript | ENST00000415822.8 | protein_coding | 1/15 | chr3 | 158803686 | |||||||
| chr3:158803955 | A | G | 1 | a0001c0001t0001g0132 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.164-364A>G | MFSD1 | ENSG00000118855.21 | transcript | ENST00000415822.8 | protein_coding | 1/15 | chr3 | 158803955 | |||||||
| chr3:158804381 | T | C | 1 | a0001c0001t0001g0059 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.216+10T>C | MFSD1 | ENSG00000118855.21 | transcript | ENST00000415822.8 | protein_coding | 2/15 | chr3 | 158804381 | |||||||
| chr3:158804395 | T | G | 1 | a0001c0001t0001g0060 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.216+24T>G | MFSD1 | ENSG00000118855.21 | transcript | ENST00000415822.8 | protein_coding | 2/15 | chr3 | 158804395 | |||||||
| chr3:158804398 | T | A | 1 | a0001c0001t0001g0142 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.216+27T>A | MFSD1 | ENSG00000118855.21 | transcript | ENST00000415822.8 | protein_coding | 2/15 | chr3 | 158804398 | |||||||
| chr3:158804401 | T | C | 3 | a0002c0002t0001g0188 a0002c0002t0001g0189 a0002c0002t0001g0190 |
3 | HG01515.hp2 HG02683.hp2 HG04199.hp1 |
intron_variant | MODIFIER | c.216+30T>C | MFSD1 | ENSG00000118855.21 | transcript | ENST00000415822.8 | protein_coding | 2/15 | chr3 | 158804401 | |||||||
| chr3:158804444 | C | G | 1 | a0001c0001t0001g0131 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.216+73C>G | MFSD1 | ENSG00000118855.21 | transcript | ENST00000415822.8 | protein_coding | 2/15 | chr3 | 158804444 | |||||||
| chr3:158804611 | G | A | 1 | a0002c0004t0001g0144 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.216+240G>A | MFSD1 | ENSG00000118855.21 | transcript | ENST00000415822.8 | protein_coding | 2/15 | chr3 | 158804611 | |||||||
| chr3:158804674 | T | C | 126 | a0001c0001t0001g0010 a0001c0001t0001g0026 a0001c0001t0001g0061 others(123): Show |
224 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(221): Show |
intron_variant | MODIFIER | c.216+303T>C | MFSD1 | ENSG00000118855.21 | transcript | ENST00000415822.8 | protein_coding | 2/15 | chr3 | 158804674 | |||||||
| chr3:158804720 | C | T | 1 | a0003c0003t0002g0187 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.216+349C>T | MFSD1 | ENSG00000118855.21 | transcript | ENST00000415822.8 | protein_coding | 2/15 | chr3 | 158804720 | |||||||
| chr3:158804807 | G | A | 4 | a0001c0001t0001g0145 a0001c0001t0001g0146 a0001c0001t0001g0147 others(1): Show |
4 | HG02109.hp1 HG02145.hp1 HG02809.hp2 others(1): Show |
intron_variant | MODIFIER | c.216+436G>A | MFSD1 | ENSG00000118855.21 | transcript | ENST00000415822.8 | protein_coding | 2/15 | chr3 | 158804807 | |||||||
| chr3:158805171 | C | T | 73 | a0001c0001t0001g0142 a0001c0001t0001g0145 a0001c0001t0001g0146 others(70): Show |
141 | HG00099.hp1 HG00140.hp2 HG00423.hp2 others(138): Show |
intron_variant | MODIFIER | c.217-191C>T | MFSD1 | ENSG00000118855.21 | transcript | ENST00000415822.8 | protein_coding | 2/15 | chr3 | 158805171 | |||||||
| chr3:158805286 | G | A | 1 | a0002c0002t0001g0191 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.217-76G>A | MFSD1 | ENSG00000118855.21 | transcript | ENST00000415822.8 | protein_coding | 2/15 | chr3 | 158805286 | |||||||
| chr3:158805512 | A | C | 1 | a0003c0003t0002g0186 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.329+38A>C | MFSD1 | ENSG00000118855.21 | transcript | ENST00000415822.8 | protein_coding | 3/15 | chr3 | 158805512 | |||||||
| chr3:158806030 | A | G | 52 | a0001c0001t0001g0010 a0001c0001t0001g0026 a0001c0001t0001g0061 others(49): Show |
80 | HG00323.hp1 HG00408.hp1 HG00558.hp2 others(77): Show |
intron_variant | MODIFIER | c.329+556A>G | MFSD1 | ENSG00000118855.21 | transcript | ENST00000415822.8 | protein_coding | 3/15 | chr3 | 158806030 | |||||||
| chr3:158806156 | A | G | 2 | a0002c0002t0005g0044 a0002c0002t0005g0143 |
3 | HG02622.hp1 HG03098.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.329+682A>G | MFSD1 | ENSG00000118855.21 | transcript | ENST00000415822.8 | protein_coding | 3/15 | chr3 | 158806156 | |||||||
| chr3:158806156 | A | T | 1 | a0002c0002t0001g0057 | 2 | HG02055.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.329+682A>T | MFSD1 | ENSG00000118855.21 | transcript | ENST00000415822.8 | protein_coding | 3/15 | chr3 | 158806156 | |||||||
| chr3:158806329 | CAGG | C | 2 | a0002c0002t0005g0044 a0002c0002t0005g0143 |
3 | HG02622.hp1 HG03098.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.330-708_330-706del others(3): Show |
MFSD1 | ENSG00000118855.21 | transcript | ENST00000415822.8 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chr3 | 158806329 | ||||||
| chr3:158806543 | T | C | 4 | a0002c0002t0003g0019 a0002c0002t0003g0020 a0002c0002t0003g0136 others(1): Show |
8 | HG01243.hp1 HG01891.hp1 HG02055.hp1 others(5): Show |
intron_variant | MODIFIER | c.330-497T>C | MFSD1 | ENSG00000118855.21 | transcript | ENST00000415822.8 | protein_coding | 3/15 | chr3 | 158806543 | |||||||
| chr3:158806587 | T | G | 1 | a0008c0010t0001g0225 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.330-453T>G | MFSD1 | ENSG00000118855.21 | transcript | ENST00000415822.8 | protein_coding | 3/15 | chr3 | 158806587 | |||||||
| chr3:158806601 | T | A | 1 | a0001c0001t0004g0063 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.330-439T>A | MFSD1 | ENSG00000118855.21 | transcript | ENST00000415822.8 | protein_coding | 3/15 | chr3 | 158806601 | |||||||
| chr3:158806780 | A | G | 30 | a0003c0003t0001g0049 a0003c0003t0001g0176 a0003c0003t0001g0183 others(27): Show |
64 | HG00280.hp1 HG00423.hp2 HG00609.hp2 others(61): Show |
intron_variant | MODIFIER | c.330-260A>G | MFSD1 | ENSG00000118855.21 | transcript | ENST00000415822.8 | protein_coding | 3/15 | chr3 | 158806780 | |||||||
| chr3:158806802 | G | A | 20 | a0001c0001t0001g0151 a0001c0001t0001g0152 a0001c0001t0001g0157 others(17): Show |
44 | HG00099.hp1 HG00140.hp2 HG00673.hp1 others(41): Show |
intron_variant | MODIFIER | c.330-238G>A | MFSD1 | ENSG00000118855.21 | transcript | ENST00000415822.8 | protein_coding | 3/15 | chr3 | 158806802 | |||||||
| chr3:158806883 | A | T | 3 | a0002c0004t0001g0163 a0002c0004t0001g0164 a0002c0004t0001g0165 |
3 | NA18975.hp2 NA19078.hp2 NA19091.hp1 |
intron_variant | MODIFIER | c.330-157A>T | MFSD1 | ENSG00000118855.21 | transcript | ENST00000415822.8 | protein_coding | 3/15 | chr3 | 158806883 | |||||||
| chr3:158806953 | T | C | 1 | a0002c0002t0001g0192 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.330-87T>C | MFSD1 | ENSG00000118855.21 | transcript | ENST00000415822.8 | protein_coding | 3/15 | chr3 | 158806953 | |||||||
| chr3:158806988 | A | AT | 6 | a0001c0001t0001g0029 a0001c0001t0001g0030 a0001c0001t0001g0056 others(3): Show |
11 | HG02145.hp2 HG02622.hp2 HG02896.hp2 others(8): Show |
intron_variant | MODIFIER | c.330-42dupT | MFSD1 | ENSG00000118855.21 | transcript | ENST00000415822.8 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chr3 | 158806988 | ||||||
| chr3:158807376 | C | G | 4 | a0002c0002t0003g0019 a0002c0002t0003g0020 a0002c0002t0003g0136 others(1): Show |
8 | HG01243.hp1 HG01891.hp1 HG02055.hp1 others(5): Show |
intron_variant | MODIFIER | c.373-20C>G | MFSD1 | ENSG00000118855.21 | transcript | ENST00000415822.8 | protein_coding | 4/15 | chr3 | 158807376 | |||||||
| chr3:158807377 | A | G | 4 | a0001c0001t0001g0042 a0001c0001t0001g0129 a0001c0001t0001g0130 others(1): Show |
5 | HG00609.hp1 HG00621.hp1 NA18964.hp1 others(2): Show |
intron_variant | MODIFIER | c.373-19A>G | MFSD1 | ENSG00000118855.21 | transcript | ENST00000415822.8 | protein_coding | 4/15 | chr3 | 158807377 | |||||||
| chr3:158807388 | C | T | 1 | a0001c0001t0001g0142 | 1 | HG03139.hp1 | splice_region_variant&intron_variant | LOW | c.373-8C>T | MFSD1 | ENSG00000118855.21 | transcript | ENST00000415822.8 | protein_coding | 4/15 | chr3 | 158807388 | |||||||
| chr3:158807533 | A | T | 5 | a0002c0002t0001g0017 a0002c0002t0001g0240 a0002c0002t0001g0241 others(2): Show |
11 | HG01255.hp1 HG01884.hp2 HG02257.hp2 others(8): Show |
intron_variant | MODIFIER | c.440+70A>T | MFSD1 | ENSG00000118855.21 | transcript | ENST00000415822.8 | protein_coding | 5/15 | chr3 | 158807533 | |||||||
| chr3:158807636 | A | G | 1 | a0003c0003t0002g0185 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.440+173A>G | MFSD1 | ENSG00000118855.21 | transcript | ENST00000415822.8 | protein_coding | 5/15 | chr3 | 158807636 | |||||||
| chr3:158807785 | T | C | 22 | a0001c0001t0001g0151 a0001c0001t0001g0152 a0001c0001t0001g0157 others(19): Show |
46 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(43): Show |
intron_variant | MODIFIER | c.440+322T>C | MFSD1 | ENSG00000118855.21 | transcript | ENST00000415822.8 | protein_coding | 5/15 | chr3 | 158807785 | |||||||
| chr3:158807961 | A | G | 3 | a0002c0004t0001g0163 a0002c0004t0001g0164 a0002c0004t0001g0165 |
3 | NA18975.hp2 NA19078.hp2 NA19091.hp1 |
intron_variant | MODIFIER | c.440+498A>G | MFSD1 | ENSG00000118855.21 | transcript | ENST00000415822.8 | protein_coding | 5/15 | chr3 | 158807961 | |||||||
| chr3:158808064 | G | A | 5 | a0002c0002t0001g0017 a0002c0002t0001g0240 a0002c0002t0001g0241 others(2): Show |
11 | HG01255.hp1 HG01884.hp2 HG02257.hp2 others(8): Show |
intron_variant | MODIFIER | c.440+601G>A | MFSD1 | ENSG00000118855.21 | transcript | ENST00000415822.8 | protein_coding | 5/15 | chr3 | 158808064 | |||||||
| chr3:158808111 | G | C | 1 | a0003c0003t0002g0166 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.440+648G>C | MFSD1 | ENSG00000118855.21 | transcript | ENST00000415822.8 | protein_coding | 5/15 | chr3 | 158808111 | |||||||
| chr3:158808301 | G | A | 4 | a0002c0002t0003g0019 a0002c0002t0003g0020 a0002c0002t0003g0136 others(1): Show |
8 | HG01243.hp1 HG01891.hp1 HG02055.hp1 others(5): Show |
intron_variant | MODIFIER | c.440+838G>A | MFSD1 | ENSG00000118855.21 | transcript | ENST00000415822.8 | protein_coding | 5/15 | chr3 | 158808301 | |||||||
| chr3:158808331 | C | T | 29 | a0003c0003t0001g0049 a0003c0003t0001g0176 a0003c0003t0001g0183 others(26): Show |
61 | HG00423.hp2 HG00609.hp2 HG01069.hp2 others(58): Show |
intron_variant | MODIFIER | c.441-848C>T | MFSD1 | ENSG00000118855.21 | transcript | ENST00000415822.8 | protein_coding | 5/15 | chr3 | 158808331 | |||||||
| chr3:158808434 | A | C | 31 | a0002c0002t0005g0044 a0002c0002t0005g0143 a0003c0003t0001g0049 others(28): Show |
64 | HG00423.hp2 HG00609.hp2 HG01069.hp2 others(61): Show |
intron_variant | MODIFIER | c.441-745A>C | MFSD1 | ENSG00000118855.21 | transcript | ENST00000415822.8 | protein_coding | 5/15 | chr3 | 158808434 | |||||||
| chr3:158808459 | G | A | 1 | a0003c0003t0002g0167 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.441-720G>A | MFSD1 | ENSG00000118855.21 | transcript | ENST00000415822.8 | protein_coding | 5/15 | chr3 | 158808459 | |||||||
| chr3:158808533 | A | G | 3 | a0001c0001t0001g0026 a0001c0001t0001g0223 a0002c0002t0001g0025 |
7 | HG01884.hp1 HG02647.hp1 HG02886.hp1 others(4): Show |
intron_variant | MODIFIER | c.441-646A>G | MFSD1 | ENSG00000118855.21 | transcript | ENST00000415822.8 | protein_coding | 5/15 | chr3 | 158808533 | |||||||
| chr3:158808688 | T | C | 1 | a0001c0001t0001g0064 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.441-491T>C | MFSD1 | ENSG00000118855.21 | transcript | ENST00000415822.8 | protein_coding | 5/15 | chr3 | 158808688 | |||||||
| chr3:158808709 | A | G | 5 | a0002c0002t0001g0138 a0002c0002t0003g0043 a0002c0002t0003g0140 others(2): Show |
6 | HG01243.hp2 HG01433.hp2 HG03041.hp1 others(3): Show |
intron_variant | MODIFIER | c.441-470A>G | MFSD1 | ENSG00000118855.21 | transcript | ENST00000415822.8 | protein_coding | 5/15 | chr3 | 158808709 | |||||||
| chr3:158808738 | T | C | 1 | a0001c0001t0001g0065 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.441-441T>C | MFSD1 | ENSG00000118855.21 | transcript | ENST00000415822.8 | protein_coding | 5/15 | chr3 | 158808738 | |||||||
| chr3:158808807 | T | G | 1 | a0002c0002t0002g0195 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.441-372T>G | MFSD1 | ENSG00000118855.21 | transcript | ENST00000415822.8 | protein_coding | 5/15 | chr3 | 158808807 | |||||||
| chr3:158808916 | T | C | 2 | a0002c0004t0001g0062 a0002c0004t0001g0149 |
2 | HG01081.hp1 HG01934.hp1 |
intron_variant | MODIFIER | c.441-263T>C | MFSD1 | ENSG00000118855.21 | transcript | ENST00000415822.8 | protein_coding | 5/15 | chr3 | 158808916 | |||||||
| chr3:158809097 | C | G | 1 | a0002c0002t0003g0015 | 4 | HG01255.hp1 HG02451.hp1 HG02723.hp2 others(1): Show |
intron_variant | MODIFIER | c.441-82C>G | MFSD1 | ENSG00000118855.21 | transcript | ENST00000415822.8 | protein_coding | 5/15 | chr3 | 158809097 | |||||||
| chr3:158809153 | G | GT | 10 | a0002c0002t0001g0017 a0002c0002t0001g0057 a0002c0002t0001g0222 others(7): Show |
17 | HG01255.hp1 HG01884.hp2 HG01934.hp1 others(14): Show |
intron_variant | MODIFIER | c.441-11dupT | MFSD1 | ENSG00000118855.21 | transcript | ENST00000415822.8 | protein_coding | 5/15 | INFO_REALIGN_3_PRIME | chr3 | 158809153 | ||||||
| chr3:158809344 | AG | A | 4 | a0001c0001t0001g0145 a0001c0001t0001g0146 a0001c0001t0001g0147 others(1): Show |
4 | HG02109.hp1 HG02145.hp1 HG02809.hp2 others(1): Show |
intron_variant | MODIFIER | c.549+58delG | MFSD1 | ENSG00000118855.21 | transcript | ENST00000415822.8 | protein_coding | 6/15 | chr3 | 158809344 | |||||||
| chr3:158809659 | A | C | 39 | a0002c0002t0001g0017 a0002c0002t0001g0240 a0002c0002t0001g0241 others(36): Show |
78 | HG00423.hp2 HG00609.hp2 HG01069.hp2 others(75): Show |
intron_variant | MODIFIER | c.549+372A>C | MFSD1 | ENSG00000118855.21 | transcript | ENST00000415822.8 | protein_coding | 6/15 | chr3 | 158809659 | |||||||
| chr3:158809708 | G | A | 4 | a0002c0002t0001g0138 a0002c0002t0003g0043 a0002c0002t0003g0140 others(1): Show |
5 | HG01243.hp2 HG01433.hp2 HG03041.hp1 others(2): Show |
intron_variant | MODIFIER | c.549+421G>A | MFSD1 | ENSG00000118855.21 | transcript | ENST00000415822.8 | protein_coding | 6/15 | chr3 | 158809708 | |||||||
| chr3:158810005 | C | T | 4 | a0001c0001t0001g0145 a0001c0001t0001g0146 a0001c0001t0001g0147 others(1): Show |
4 | HG02109.hp1 HG02145.hp1 HG02809.hp2 others(1): Show |
intron_variant | MODIFIER | c.549+718C>T | MFSD1 | ENSG00000118855.21 | transcript | ENST00000415822.8 | protein_coding | 6/15 | chr3 | 158810005 | |||||||
| chr3:158810047 | C | T | 1 | a0002c0002t0003g0140 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.549+760C>T | MFSD1 | ENSG00000118855.21 | transcript | ENST00000415822.8 | protein_coding | 6/15 | chr3 | 158810047 | |||||||
| chr3:158810082 | C | T | 3 | a0002c0002t0003g0020 a0002c0002t0003g0136 a0002c0002t0003g0137 |
5 | HG01891.hp1 HG02055.hp1 HG02622.hp2 others(2): Show |
intron_variant | MODIFIER | c.549+795C>T | MFSD1 | ENSG00000118855.21 | transcript | ENST00000415822.8 | protein_coding | 6/15 | chr3 | 158810082 | |||||||
| chr3:158810239 | C | T | 2 | a0001c0001t0001g0126 a0001c0001t0001g0127 |
2 | NA19060.hp2 NA19067.hp2 |
intron_variant | MODIFIER | c.549+952C>T | MFSD1 | ENSG00000118855.21 | transcript | ENST00000415822.8 | protein_coding | 6/15 | chr3 | 158810239 | |||||||
| chr3:158810246 | G | A | 1 | a0002c0002t0003g0020 | 3 | HG01891.hp1 HG02055.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.549+959G>A | MFSD1 | ENSG00000118855.21 | transcript | ENST00000415822.8 | protein_coding | 6/15 | chr3 | 158810246 | |||||||
| chr3:158810318 | A | T | 1 | a0002c0008t0001g0221 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.549+1031A>T | MFSD1 | ENSG00000118855.21 | transcript | ENST00000415822.8 | protein_coding | 6/15 | chr3 | 158810318 | |||||||
| chr3:158810460 | A | T | 1 | a0002c0002t0001g0125 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.549+1173A>T | MFSD1 | ENSG00000118855.21 | transcript | ENST00000415822.8 | protein_coding | 6/15 | chr3 | 158810460 | |||||||
| chr3:158810468 | A | G | 3 | a0002c0004t0001g0163 a0002c0004t0001g0164 a0002c0004t0001g0165 |
3 | NA18975.hp2 NA19078.hp2 NA19091.hp1 |
intron_variant | MODIFIER | c.549+1181A>G | MFSD1 | ENSG00000118855.21 | transcript | ENST00000415822.8 | protein_coding | 6/15 | chr3 | 158810468 | |||||||
| chr3:158810531 | C | T | 4 | a0001c0001t0001g0145 a0001c0001t0001g0146 a0001c0001t0001g0147 others(1): Show |
4 | HG02109.hp1 HG02145.hp1 HG02809.hp2 others(1): Show |
intron_variant | MODIFIER | c.549+1244C>T | MFSD1 | ENSG00000118855.21 | transcript | ENST00000415822.8 | protein_coding | 6/15 | chr3 | 158810531 | |||||||
| chr3:158810676 | C | T | 1 | a0002c0002t0001g0220 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.549+1389C>T | MFSD1 | ENSG00000118855.21 | transcript | ENST00000415822.8 | protein_coding | 6/15 | chr3 | 158810676 | |||||||
| chr3:158810877 | A | T | 1 | a0002c0004t0001g0162 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.549+1590A>T | MFSD1 | ENSG00000118855.21 | transcript | ENST00000415822.8 | protein_coding | 6/15 | chr3 | 158810877 | |||||||
| chr3:158810940 | A | G | 1 | a0003c0003t0001g0183 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.549+1653A>G | MFSD1 | ENSG00000118855.21 | transcript | ENST00000415822.8 | protein_coding | 6/15 | chr3 | 158810940 | |||||||
| chr3:158811055 | C | T | 5 | a0002c0002t0001g0138 a0002c0002t0003g0043 a0002c0002t0003g0140 others(2): Show |
6 | HG01243.hp2 HG01433.hp2 HG03041.hp1 others(3): Show |
intron_variant | MODIFIER | c.549+1768C>T | MFSD1 | ENSG00000118855.21 | transcript | ENST00000415822.8 | protein_coding | 6/15 | chr3 | 158811055 | |||||||
| chr3:158811103 | C | T | 4 | a0002c0002t0001g0138 a0002c0002t0003g0043 a0002c0002t0003g0140 others(1): Show |
5 | HG01243.hp2 HG01433.hp2 HG03041.hp1 others(2): Show |
intron_variant | MODIFIER | c.549+1816C>T | MFSD1 | ENSG00000118855.21 | transcript | ENST00000415822.8 | protein_coding | 6/15 | chr3 | 158811103 | |||||||
| chr3:158811328 | G | A | 60 | a0001c0001t0001g0151 a0001c0001t0001g0152 a0001c0001t0001g0157 others(57): Show |
123 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(120): Show |
intron_variant | MODIFIER | c.549+2041G>A | MFSD1 | ENSG00000118855.21 | transcript | ENST00000415822.8 | protein_coding | 6/15 | chr3 | 158811328 | |||||||
| chr3:158811329 | T | C | 1 | a0002c0004t0001g0150 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.549+2042T>C | MFSD1 | ENSG00000118855.21 | transcript | ENST00000415822.8 | protein_coding | 6/15 | chr3 | 158811329 | |||||||
| chr3:158811483 | A | G | 5 | a0002c0002t0001g0138 a0002c0002t0003g0043 a0002c0002t0003g0140 others(2): Show |
6 | HG01243.hp2 HG01433.hp2 HG03041.hp1 others(3): Show |
intron_variant | MODIFIER | c.549+2196A>G | MFSD1 | ENSG00000118855.21 | transcript | ENST00000415822.8 | protein_coding | 6/15 | chr3 | 158811483 | |||||||
| chr3:158811828 | G | A | 1 | a0003c0003t0001g0183 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.550-2137G>A | MFSD1 | ENSG00000118855.21 | transcript | ENST00000415822.8 | protein_coding | 6/15 | chr3 | 158811828 | |||||||
| chr3:158812098 | G | A | 1 | a0002c0002t0001g0188 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.550-1867G>A | MFSD1 | ENSG00000118855.21 | transcript | ENST00000415822.8 | protein_coding | 6/15 | chr3 | 158812098 | |||||||
| chr3:158812147 | T | C | 1 | a0002c0002t0001g0051 | 2 | HG00738.hp1 HG01167.hp1 |
intron_variant | MODIFIER | c.550-1818T>C | MFSD1 | ENSG00000118855.21 | transcript | ENST00000415822.8 | protein_coding | 6/15 | chr3 | 158812147 | |||||||
| chr3:158812161 | A | G | 1 | a0001c0001t0001g0124 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.550-1804A>G | MFSD1 | ENSG00000118855.21 | transcript | ENST00000415822.8 | protein_coding | 6/15 | chr3 | 158812161 | |||||||
| chr3:158812276 | C | T | 5 | a0002c0002t0001g0017 a0002c0002t0001g0240 a0002c0002t0001g0241 others(2): Show |
11 | HG01255.hp1 HG01884.hp2 HG02257.hp2 others(8): Show |
intron_variant | MODIFIER | c.550-1689C>T | MFSD1 | ENSG00000118855.21 | transcript | ENST00000415822.8 | protein_coding | 6/15 | chr3 | 158812276 | |||||||
| chr3:158812295 | A | G | 1 | a0002c0002t0001g0192 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.550-1670A>G | MFSD1 | ENSG00000118855.21 | transcript | ENST00000415822.8 | protein_coding | 6/15 | chr3 | 158812295 | |||||||
| chr3:158812353 | A | G | 1 | a0002c0002t0001g0219 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.550-1612A>G | MFSD1 | ENSG00000118855.21 | transcript | ENST00000415822.8 | protein_coding | 6/15 | chr3 | 158812353 | |||||||
| chr3:158812400 | G | A | 1 | a0003c0003t0002g0168 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.550-1565G>A | MFSD1 | ENSG00000118855.21 | transcript | ENST00000415822.8 | protein_coding | 6/15 | chr3 | 158812400 | |||||||
| chr3:158812834 | C | T | 21 | a0001c0001t0001g0151 a0001c0001t0001g0152 a0001c0001t0001g0157 others(18): Show |
45 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(42): Show |
intron_variant | MODIFIER | c.550-1131C>T | MFSD1 | ENSG00000118855.21 | transcript | ENST00000415822.8 | protein_coding | 6/15 | chr3 | 158812834 | |||||||
| chr3:158812905 | G | A | 1 | a0001c0001t0001g0132 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.550-1060G>A | MFSD1 | ENSG00000118855.21 | transcript | ENST00000415822.8 | protein_coding | 6/15 | chr3 | 158812905 | |||||||
| chr3:158813052 | T | C | 4 | a0001c0001t0001g0145 a0001c0001t0001g0146 a0001c0001t0001g0147 others(1): Show |
4 | HG02109.hp1 HG02145.hp1 HG02809.hp2 others(1): Show |
intron_variant | MODIFIER | c.550-913T>C | MFSD1 | ENSG00000118855.21 | transcript | ENST00000415822.8 | protein_coding | 6/15 | chr3 | 158813052 | |||||||
| chr3:158813105 | CT | C | 6 | a0001c0001t0001g0066 a0001c0001t0001g0145 a0001c0001t0001g0146 others(3): Show |
8 | HG01168.hp2 HG01243.hp1 HG02109.hp1 others(5): Show |
intron_variant | MODIFIER | c.550-848delT | MFSD1 | ENSG00000118855.21 | transcript | ENST00000415822.8 | protein_coding | 6/15 | INFO_REALIGN_3_PRIME | chr3 | 158813105 | ||||||
| chr3:158813152 | C | CT | 8 | a0001c0001t0001g0010 a0001c0001t0001g0123 a0001c0001t0006g0010 others(5): Show |
20 | HG00408.hp1 HG01074.hp1 HG01192.hp2 others(17): Show |
intron_variant | MODIFIER | c.550-800dupT | MFSD1 | ENSG00000118855.21 | transcript | ENST00000415822.8 | protein_coding | 6/15 | INFO_REALIGN_3_PRIME | chr3 | 158813152 | ||||||
| chr3:158813171 | G | A | 1 | a0001c0001t0001g0067 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.550-794G>A | MFSD1 | ENSG00000118855.21 | transcript | ENST00000415822.8 | protein_coding | 6/15 | chr3 | 158813171 | |||||||
| chr3:158813297 | G | A | 1 | a0001c0001t0001g0068 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.550-668G>A | MFSD1 | ENSG00000118855.21 | transcript | ENST00000415822.8 | protein_coding | 6/15 | chr3 | 158813297 | |||||||
| chr3:158813376 | G | T | 21 | a0001c0001t0001g0151 a0001c0001t0001g0152 a0001c0001t0001g0157 others(18): Show |
45 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(42): Show |
intron_variant | MODIFIER | c.550-589G>T | MFSD1 | ENSG00000118855.21 | transcript | ENST00000415822.8 | protein_coding | 6/15 | chr3 | 158813376 | |||||||
| chr3:158813568 | C | G | 1 | a0002c0002t0003g0019 | 3 | HG01243.hp1 HG02280.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.550-397C>G | MFSD1 | ENSG00000118855.21 | transcript | ENST00000415822.8 | protein_coding | 6/15 | chr3 | 158813568 | |||||||
| chr3:158813764 | C | CT | 4 | a0001c0001t0001g0122 a0002c0002t0001g0192 a0002c0002t0003g0020 others(1): Show |
6 | HG01891.hp1 HG02055.hp1 HG03471.hp2 others(3): Show |
intron_variant | MODIFIER | c.550-186dupT | MFSD1 | ENSG00000118855.21 | transcript | ENST00000415822.8 | protein_coding | 6/15 | INFO_REALIGN_3_PRIME | chr3 | 158813764 | ||||||
| chr3:158813764 | CT | C | 51 | a0001c0001t0001g0026 a0001c0001t0001g0031 a0001c0001t0001g0069 others(48): Show |
90 | HG00280.hp1 HG00423.hp2 HG00609.hp2 others(87): Show |
intron_variant | MODIFIER | c.550-186delT | MFSD1 | ENSG00000118855.21 | transcript | ENST00000415822.8 | protein_coding | 6/15 | INFO_REALIGN_3_PRIME | chr3 | 158813764 | ||||||
| chr3:158813764 | CTT | C | 21 | a0001c0001t0001g0151 a0001c0001t0001g0152 a0001c0001t0001g0157 others(18): Show |
45 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(42): Show |
intron_variant | MODIFIER | c.550-187_550-186del others(2): Show |
MFSD1 | ENSG00000118855.21 | transcript | ENST00000415822.8 | protein_coding | 6/15 | INFO_REALIGN_3_PRIME | chr3 | 158813764 | ||||||
| chr3:158814138 | G | A | 3 | a0002c0004t0001g0163 a0002c0004t0001g0164 a0002c0004t0001g0165 |
3 | NA18975.hp2 NA19078.hp2 NA19091.hp1 |
intron_variant | MODIFIER | c.652+71G>A | MFSD1 | ENSG00000118855.21 | transcript | ENST00000415822.8 | protein_coding | 7/15 | chr3 | 158814138 | |||||||
| chr3:158814185 | A | T | 30 | a0003c0003t0001g0049 a0003c0003t0001g0176 a0003c0003t0001g0183 others(27): Show |
64 | HG00280.hp1 HG00423.hp2 HG00609.hp2 others(61): Show |
intron_variant | MODIFIER | c.652+118A>T | MFSD1 | ENSG00000118855.21 | transcript | ENST00000415822.8 | protein_coding | 7/15 | chr3 | 158814185 | |||||||
| chr3:158814295 | C | T | 1 | a0002c0002t0001g0198 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.652+228C>T | MFSD1 | ENSG00000118855.21 | transcript | ENST00000415822.8 | protein_coding | 7/15 | chr3 | 158814295 | |||||||
| chr3:158814383 | C | T | 5 | a0002c0002t0001g0017 a0002c0002t0001g0240 a0002c0002t0001g0241 others(2): Show |
11 | HG01255.hp1 HG01884.hp2 HG02257.hp2 others(8): Show |
intron_variant | MODIFIER | c.652+316C>T | MFSD1 | ENSG00000118855.21 | transcript | ENST00000415822.8 | protein_coding | 7/15 | chr3 | 158814383 | |||||||
| chr3:158814563 | C | T | 1 | a0001c0001t0001g0121 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.652+496C>T | MFSD1 | ENSG00000118855.21 | transcript | ENST00000415822.8 | protein_coding | 7/15 | chr3 | 158814563 | |||||||
| chr3:158814565 | C | T | 8 | a0002c0002t0001g0008 a0002c0002t0001g0009 a0002c0002t0001g0024 others(5): Show |
20 | HG01074.hp1 HG01257.hp2 HG01258.hp2 others(17): Show |
intron_variant | MODIFIER | c.652+498C>T | MFSD1 | ENSG00000118855.21 | transcript | ENST00000415822.8 | protein_coding | 7/15 | chr3 | 158814565 | |||||||
| chr3:158814611 | G | A | 4 | a0001c0001t0001g0032 a0001c0001t0001g0074 a0001c0001t0001g0075 others(1): Show |
5 | HG02165.hp1 NA18612.hp1 NA18949.hp2 others(2): Show |
intron_variant | MODIFIER | c.652+544G>A | MFSD1 | ENSG00000118855.21 | transcript | ENST00000415822.8 | protein_coding | 7/15 | chr3 | 158814611 | |||||||
| chr3:158814616 | T | C | 61 | a0001c0001t0001g0151 a0001c0001t0001g0152 a0001c0001t0001g0157 others(58): Show |
126 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(123): Show |
intron_variant | MODIFIER | c.652+549T>C | MFSD1 | ENSG00000118855.21 | transcript | ENST00000415822.8 | protein_coding | 7/15 | chr3 | 158814616 | |||||||
| chr3:158814734 | G | A | 3 | a0002c0004t0001g0163 a0002c0004t0001g0164 a0002c0004t0001g0165 |
3 | NA18975.hp2 NA19078.hp2 NA19091.hp1 |
intron_variant | MODIFIER | c.652+667G>A | MFSD1 | ENSG00000118855.21 | transcript | ENST00000415822.8 | protein_coding | 7/15 | chr3 | 158814734 | |||||||
| chr3:158814852 | G | A | 2 | a0002c0002t0005g0044 a0002c0002t0005g0143 |
3 | HG02622.hp1 HG03098.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.652+785G>A | MFSD1 | ENSG00000118855.21 | transcript | ENST00000415822.8 | protein_coding | 7/15 | chr3 | 158814852 | |||||||
| chr3:158814860 | A | T | 1 | a0002c0002t0001g0215 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.652+793A>T | MFSD1 | ENSG00000118855.21 | transcript | ENST00000415822.8 | protein_coding | 7/15 | chr3 | 158814860 | |||||||
| chr3:158814910 | C | T | 3 | a0001c0001t0001g0118 a0001c0001t0001g0119 a0001c0001t0001g0120 |
3 | HG00323.hp2 HG01361.hp1 HG01496.hp2 |
intron_variant | MODIFIER | c.652+843C>T | MFSD1 | ENSG00000118855.21 | transcript | ENST00000415822.8 | protein_coding | 7/15 | chr3 | 158814910 | |||||||
| chr3:158814953 | A | C | 40 | a0002c0002t0001g0017 a0002c0002t0001g0240 a0002c0002t0001g0241 others(37): Show |
81 | HG00280.hp1 HG00423.hp2 HG00609.hp2 others(78): Show |
intron_variant | MODIFIER | c.652+886A>C | MFSD1 | ENSG00000118855.21 | transcript | ENST00000415822.8 | protein_coding | 7/15 | chr3 | 158814953 | |||||||
| chr3:158814980 | G | A | 2 | a0001c0001t0001g0126 a0001c0001t0001g0127 |
2 | NA19060.hp2 NA19067.hp2 |
intron_variant | MODIFIER | c.652+913G>A | MFSD1 | ENSG00000118855.21 | transcript | ENST00000415822.8 | protein_coding | 7/15 | chr3 | 158814980 | |||||||
| chr3:158815356 | C | CT | 167 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0007 others(164): Show |
257 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(254): Show |
intron_variant | MODIFIER | c.652+1305dupT | MFSD1 | ENSG00000118855.21 | transcript | ENST00000415822.8 | protein_coding | 7/15 | INFO_REALIGN_3_PRIME | chr3 | 158815356 | ||||||
| chr3:158815356 | C | CTT | 10 | a0001c0001t0001g0116 a0001c0001t0001g0117 a0002c0002t0001g0017 others(7): Show |
17 | HG00558.hp1 HG01255.hp1 HG01884.hp2 others(14): Show |
intron_variant | MODIFIER | c.652+1304_652+1305d others(4): Show |
MFSD1 | ENSG00000118855.21 | transcript | ENST00000415822.8 | protein_coding | 7/15 | INFO_REALIGN_3_PRIME | chr3 | 158815356 | ||||||
| chr3:158815356 | CT | C | 23 | a0001c0001t0001g0151 a0001c0001t0001g0152 a0001c0001t0001g0157 others(20): Show |
48 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(45): Show |
intron_variant | MODIFIER | c.652+1305delT | MFSD1 | ENSG00000118855.21 | transcript | ENST00000415822.8 | protein_coding | 7/15 | INFO_REALIGN_3_PRIME | chr3 | 158815356 | ||||||
| chr3:158815672 | C | CT | 2 | a0001c0001t0001g0010 a0001c0001t0006g0010 |
4 | HG00408.hp1 HG01192.hp2 HG02148.hp2 others(1): Show |
intron_variant | MODIFIER | c.652+1608dupT | MFSD1 | ENSG00000118855.21 | transcript | ENST00000415822.8 | protein_coding | 7/15 | INFO_REALIGN_3_PRIME | chr3 | 158815672 | ||||||
| chr3:158815726 | A | C | 1 | a0002c0004t0001g0160 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.652+1659A>C | MFSD1 | ENSG00000118855.21 | transcript | ENST00000415822.8 | protein_coding | 7/15 | chr3 | 158815726 | |||||||
| chr3:158815760 | G | A | 3 | a0002c0004t0001g0163 a0002c0004t0001g0164 a0002c0004t0001g0165 |
3 | NA18975.hp2 NA19078.hp2 NA19091.hp1 |
intron_variant | MODIFIER | c.652+1693G>A | MFSD1 | ENSG00000118855.21 | transcript | ENST00000415822.8 | protein_coding | 7/15 | chr3 | 158815760 | |||||||
| chr3:158815801 | T | C | 1 | a0002c0004t0001g0082 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.652+1734T>C | MFSD1 | ENSG00000118855.21 | transcript | ENST00000415822.8 | protein_coding | 7/15 | chr3 | 158815801 | |||||||
| chr3:158815817 | C | A | 1 | a0001c0001t0001g0083 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.652+1750C>A | MFSD1 | ENSG00000118855.21 | transcript | ENST00000415822.8 | protein_coding | 7/15 | chr3 | 158815817 | |||||||
| chr3:158815851 | T | C | 1 | a0002c0002t0001g0188 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.652+1784T>C | MFSD1 | ENSG00000118855.21 | transcript | ENST00000415822.8 | protein_coding | 7/15 | chr3 | 158815851 | |||||||
| chr3:158815882 | C | A | 29 | a0003c0003t0001g0049 a0003c0003t0001g0176 a0003c0003t0001g0183 others(26): Show |
61 | HG00423.hp2 HG00609.hp2 HG01069.hp2 others(58): Show |
intron_variant | MODIFIER | c.652+1815C>A | MFSD1 | ENSG00000118855.21 | transcript | ENST00000415822.8 | protein_coding | 7/15 | chr3 | 158815882 | |||||||
| chr3:158816042 | C | G | 2 | a0002c0004t0001g0046 a0002c0004t0001g0144 |
3 | NA18939.hp1 NA19012.hp1 NA19081.hp2 |
intron_variant | MODIFIER | c.652+1975C>G | MFSD1 | ENSG00000118855.21 | transcript | ENST00000415822.8 | protein_coding | 7/15 | chr3 | 158816042 | |||||||
| chr3:158816159 | G | A | 1 | a0001c0001t0001g0074 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.652+2092G>A | MFSD1 | ENSG00000118855.21 | transcript | ENST00000415822.8 | protein_coding | 7/15 | chr3 | 158816159 | |||||||
| chr3:158816224 | G | A | 2 | a0001c0001t0001g0151 a0001c0001t0001g0152 |
2 | HG00673.hp1 NA18957.hp2 |
intron_variant | MODIFIER | c.652+2157G>A | MFSD1 | ENSG00000118855.21 | transcript | ENST00000415822.8 | protein_coding | 7/15 | chr3 | 158816224 | |||||||
| chr3:158816231 | C | T | 21 | a0001c0001t0001g0151 a0001c0001t0001g0152 a0001c0001t0001g0157 others(18): Show |
45 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(42): Show |
intron_variant | MODIFIER | c.652+2164C>T | MFSD1 | ENSG00000118855.21 | transcript | ENST00000415822.8 | protein_coding | 7/15 | chr3 | 158816231 | |||||||
| chr3:158816301 | C | G | 5 | a0002c0002t0001g0017 a0002c0002t0001g0240 a0002c0002t0001g0241 others(2): Show |
11 | HG01255.hp1 HG01884.hp2 HG02257.hp2 others(8): Show |
intron_variant | MODIFIER | c.652+2234C>G | MFSD1 | ENSG00000118855.21 | transcript | ENST00000415822.8 | protein_coding | 7/15 | chr3 | 158816301 | |||||||
| chr3:158816322 | C | T | 13 | a0001c0001t0001g0016 a0001c0001t0001g0028 a0001c0001t0001g0029 others(10): Show |
23 | HG00140.hp1 HG00639.hp2 HG00733.hp2 others(20): Show |
intron_variant | MODIFIER | c.652+2255C>T | MFSD1 | ENSG00000118855.21 | transcript | ENST00000415822.8 | protein_coding | 7/15 | chr3 | 158816322 | |||||||
| chr3:158816339 | C | A | 1 | a0002c0002t0001g0189 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.652+2272C>A | MFSD1 | ENSG00000118855.21 | transcript | ENST00000415822.8 | protein_coding | 7/15 | chr3 | 158816339 | |||||||
| chr3:158816340 | G | A | 36 | a0002c0002t0001g0017 a0002c0002t0001g0240 a0002c0002t0001g0241 others(33): Show |
75 | HG00423.hp2 HG00609.hp2 HG01069.hp2 others(72): Show |
intron_variant | MODIFIER | c.652+2273G>A | MFSD1 | ENSG00000118855.21 | transcript | ENST00000415822.8 | protein_coding | 7/15 | chr3 | 158816340 | |||||||
| chr3:158816360 | A | G | 1 | a0001c0001t0001g0115 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.652+2293A>G | MFSD1 | ENSG00000118855.21 | transcript | ENST00000415822.8 | protein_coding | 7/15 | chr3 | 158816360 | |||||||
| chr3:158816371 | T | C | 1 | a0001c0001t0001g0145 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.652+2304T>C | MFSD1 | ENSG00000118855.21 | transcript | ENST00000415822.8 | protein_coding | 7/15 | chr3 | 158816371 | |||||||
| chr3:158816418 | T | C | 3 | a0002c0002t0003g0020 a0002c0002t0003g0136 a0002c0002t0003g0137 |
5 | HG01891.hp1 HG02055.hp1 HG02622.hp2 others(2): Show |
intron_variant | MODIFIER | c.652+2351T>C | MFSD1 | ENSG00000118855.21 | transcript | ENST00000415822.8 | protein_coding | 7/15 | chr3 | 158816418 | |||||||
| chr3:158816426 | G | A | 1 | a0001c0001t0012g0084 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.652+2359G>A | MFSD1 | ENSG00000118855.21 | transcript | ENST00000415822.8 | protein_coding | 7/15 | chr3 | 158816426 | |||||||
| chr3:158816468 | G | A | 5 | a0002c0002t0001g0017 a0002c0002t0001g0240 a0002c0002t0001g0241 others(2): Show |
11 | HG01255.hp1 HG01884.hp2 HG02257.hp2 others(8): Show |
intron_variant | MODIFIER | c.652+2401G>A | MFSD1 | ENSG00000118855.21 | transcript | ENST00000415822.8 | protein_coding | 7/15 | chr3 | 158816468 | |||||||
| chr3:158816502 | T | A | 1 | a0001c0001t0001g0232 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.652+2435T>A | MFSD1 | ENSG00000118855.21 | transcript | ENST00000415822.8 | protein_coding | 7/15 | chr3 | 158816502 | |||||||
| chr3:158816533 | G | A | 1 | a0002c0002t0001g0192 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.652+2466G>A | MFSD1 | ENSG00000118855.21 | transcript | ENST00000415822.8 | protein_coding | 7/15 | chr3 | 158816533 | |||||||
| chr3:158816574 | C | T | 1 | a0001c0001t0001g0073 | 1 | NA19064.hp2 | intron_variant | MODIFIER | c.652+2507C>T | MFSD1 | ENSG00000118855.21 | transcript | ENST00000415822.8 | protein_coding | 7/15 | chr3 | 158816574 | |||||||
| chr3:158816704 | T | G | 1 | a0004c0005t0001g0199 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.652+2637T>G | MFSD1 | ENSG00000118855.21 | transcript | ENST00000415822.8 | protein_coding | 7/15 | chr3 | 158816704 | |||||||
| chr3:158816791 | G | A | 3 | a0001c0001t0001g0145 a0001c0001t0001g0146 a0001c0001t0001g0147 |
3 | HG02109.hp1 HG02145.hp1 HG02809.hp2 |
intron_variant | MODIFIER | c.652+2724G>A | MFSD1 | ENSG00000118855.21 | transcript | ENST00000415822.8 | protein_coding | 7/15 | chr3 | 158816791 | |||||||
| chr3:158816829 | C | A | 73 | a0001c0001t0001g0145 a0001c0001t0001g0146 a0001c0001t0001g0147 others(70): Show |
141 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(138): Show |
intron_variant | MODIFIER | c.652+2762C>A | MFSD1 | ENSG00000118855.21 | transcript | ENST00000415822.8 | protein_coding | 7/15 | chr3 | 158816829 | |||||||
| chr3:158816833 | G | T | 73 | a0001c0001t0001g0145 a0001c0001t0001g0146 a0001c0001t0001g0147 others(70): Show |
141 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(138): Show |
intron_variant | MODIFIER | c.652+2766G>T | MFSD1 | ENSG00000118855.21 | transcript | ENST00000415822.8 | protein_coding | 7/15 | chr3 | 158816833 | |||||||
| chr3:158816932 | C | A | 60 | a0001c0001t0001g0151 a0001c0001t0001g0152 a0001c0001t0001g0157 others(57): Show |
123 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(120): Show |
intron_variant | MODIFIER | c.653-2717C>A | MFSD1 | ENSG00000118855.21 | transcript | ENST00000415822.8 | protein_coding | 7/15 | chr3 | 158816932 | |||||||
| chr3:158817014 | C | G | 21 | a0001c0001t0001g0151 a0001c0001t0001g0152 a0001c0001t0001g0157 others(18): Show |
45 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(42): Show |
intron_variant | MODIFIER | c.653-2635C>G | MFSD1 | ENSG00000118855.21 | transcript | ENST00000415822.8 | protein_coding | 7/15 | chr3 | 158817014 | |||||||
| chr3:158817032 | C | T | 1 | a0002c0002t0001g0219 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.653-2617C>T | MFSD1 | ENSG00000118855.21 | transcript | ENST00000415822.8 | protein_coding | 7/15 | chr3 | 158817032 | |||||||
| chr3:158817163 | G | A | 1 | a0002c0002t0001g0227 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.653-2486G>A | MFSD1 | ENSG00000118855.21 | transcript | ENST00000415822.8 | protein_coding | 7/15 | chr3 | 158817163 | |||||||
| chr3:158817173 | C | T | 3 | a0002c0002t0003g0020 a0002c0002t0003g0136 a0002c0002t0003g0137 |
5 | HG01891.hp1 HG02055.hp1 HG02622.hp2 others(2): Show |
intron_variant | MODIFIER | c.653-2476C>T | MFSD1 | ENSG00000118855.21 | transcript | ENST00000415822.8 | protein_coding | 7/15 | chr3 | 158817173 | |||||||
| chr3:158817213 | A | G | 1 | a0002c0004t0001g0141 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.653-2436A>G | MFSD1 | ENSG00000118855.21 | transcript | ENST00000415822.8 | protein_coding | 7/15 | chr3 | 158817213 | |||||||
| chr3:158817280 | A | T | 1 | a0003c0003t0002g0181 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.653-2369A>T | MFSD1 | ENSG00000118855.21 | transcript | ENST00000415822.8 | protein_coding | 7/15 | chr3 | 158817280 | |||||||
| chr3:158817326 | A | G | 3 | a0002c0004t0001g0163 a0002c0004t0001g0164 a0002c0004t0001g0165 |
3 | NA18975.hp2 NA19078.hp2 NA19091.hp1 |
intron_variant | MODIFIER | c.653-2323A>G | MFSD1 | ENSG00000118855.21 | transcript | ENST00000415822.8 | protein_coding | 7/15 | chr3 | 158817326 | |||||||
| chr3:158817454 | A | C | 1 | a0003c0003t0002g0180 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.653-2195A>C | MFSD1 | ENSG00000118855.21 | transcript | ENST00000415822.8 | protein_coding | 7/15 | chr3 | 158817454 | |||||||
| chr3:158817618 | G | A | 21 | a0001c0001t0001g0151 a0001c0001t0001g0152 a0001c0001t0001g0157 others(18): Show |
45 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(42): Show |
intron_variant | MODIFIER | c.653-2031G>A | MFSD1 | ENSG00000118855.21 | transcript | ENST00000415822.8 | protein_coding | 7/15 | chr3 | 158817618 | |||||||
| chr3:158817775 | A | G | 3 | a0001c0001t0001g0113 a0001c0001t0001g0114 a0001c0001t0001g0115 |
3 | HG01109.hp2 HG01123.hp2 HG02602.hp2 |
intron_variant | MODIFIER | c.653-1874A>G | MFSD1 | ENSG00000118855.21 | transcript | ENST00000415822.8 | protein_coding | 7/15 | chr3 | 158817775 | |||||||
| chr3:158817830 | C | T | 1 | a0001c0001t0001g0112 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.653-1819C>T | MFSD1 | ENSG00000118855.21 | transcript | ENST00000415822.8 | protein_coding | 7/15 | chr3 | 158817830 | |||||||
| chr3:158817939 | A | G | 1 | a0002c0002t0001g0214 | 1 | HG01517.hp1 | intron_variant | MODIFIER | c.653-1710A>G | MFSD1 | ENSG00000118855.21 | transcript | ENST00000415822.8 | protein_coding | 7/15 | chr3 | 158817939 | |||||||
| chr3:158817952 | A | C | 2 | a0002c0002t0001g0212 a0002c0002t0001g0213 |
2 | HG03130.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.653-1697A>C | MFSD1 | ENSG00000118855.21 | transcript | ENST00000415822.8 | protein_coding | 7/15 | chr3 | 158817952 | |||||||
| chr3:158817956 | G | A | 3 | a0002c0002t0001g0017 a0002c0002t0001g0240 a0002c0002t0001g0241 |
6 | HG01884.hp2 HG02258.hp2 HG02818.hp1 others(3): Show |
intron_variant | MODIFIER | c.653-1693G>A | MFSD1 | ENSG00000118855.21 | transcript | ENST00000415822.8 | protein_coding | 7/15 | chr3 | 158817956 | |||||||
| chr3:158817956 | G | T | 21 | a0001c0001t0001g0151 a0001c0001t0001g0152 a0001c0001t0001g0157 others(18): Show |
45 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(42): Show |
intron_variant | MODIFIER | c.653-1693G>T | MFSD1 | ENSG00000118855.21 | transcript | ENST00000415822.8 | protein_coding | 7/15 | chr3 | 158817956 | |||||||
| chr3:158818089 | G | A | 2 | a0002c0004t0001g0046 a0002c0004t0001g0144 |
3 | NA18939.hp1 NA19012.hp1 NA19081.hp2 |
intron_variant | MODIFIER | c.653-1560G>A | MFSD1 | ENSG00000118855.21 | transcript | ENST00000415822.8 | protein_coding | 7/15 | chr3 | 158818089 | |||||||
| chr3:158818137 | C | T | 4 | a0001c0001t0001g0145 a0001c0001t0001g0146 a0001c0001t0001g0147 others(1): Show |
4 | HG02109.hp1 HG02145.hp1 HG02809.hp2 others(1): Show |
intron_variant | MODIFIER | c.653-1512C>T | MFSD1 | ENSG00000118855.21 | transcript | ENST00000415822.8 | protein_coding | 7/15 | chr3 | 158818137 | |||||||
| chr3:158818161 | A | G | 2 | a0002c0002t0003g0015 a0006c0009t0003g0224 |
5 | HG01255.hp1 HG02257.hp2 HG02451.hp1 others(2): Show |
intron_variant | MODIFIER | c.653-1488A>G | MFSD1 | ENSG00000118855.21 | transcript | ENST00000415822.8 | protein_coding | 7/15 | chr3 | 158818161 | |||||||
| chr3:158818162 | T | C | 61 | a0001c0001t0001g0151 a0001c0001t0001g0152 a0001c0001t0001g0157 others(58): Show |
126 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(123): Show |
intron_variant | MODIFIER | c.653-1487T>C | MFSD1 | ENSG00000118855.21 | transcript | ENST00000415822.8 | protein_coding | 7/15 | chr3 | 158818162 | |||||||
| chr3:158818174 | A | C | 4 | a0001c0001t0001g0145 a0001c0001t0001g0146 a0001c0001t0001g0147 others(1): Show |
4 | HG02109.hp1 HG02145.hp1 HG02809.hp2 others(1): Show |
intron_variant | MODIFIER | c.653-1475A>C | MFSD1 | ENSG00000118855.21 | transcript | ENST00000415822.8 | protein_coding | 7/15 | chr3 | 158818174 | |||||||
| chr3:158818251 | T | C | 1 | a0001c0001t0001g0142 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.653-1398T>C | MFSD1 | ENSG00000118855.21 | transcript | ENST00000415822.8 | protein_coding | 7/15 | chr3 | 158818251 | |||||||
| chr3:158818286 | A | G | 39 | a0002c0002t0001g0017 a0002c0002t0001g0240 a0002c0002t0001g0241 others(36): Show |
78 | HG00423.hp2 HG00609.hp2 HG01069.hp2 others(75): Show |
intron_variant | MODIFIER | c.653-1363A>G | MFSD1 | ENSG00000118855.21 | transcript | ENST00000415822.8 | protein_coding | 7/15 | chr3 | 158818286 | |||||||
| chr3:158818334 | C | T | 36 | a0002c0002t0001g0017 a0002c0002t0001g0240 a0002c0002t0001g0241 others(33): Show |
75 | HG00423.hp2 HG00609.hp2 HG01069.hp2 others(72): Show |
intron_variant | MODIFIER | c.653-1315C>T | MFSD1 | ENSG00000118855.21 | transcript | ENST00000415822.8 | protein_coding | 7/15 | chr3 | 158818334 | |||||||
| chr3:158818359 | A | G | 1 | a0002c0002t0005g0143 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.653-1290A>G | MFSD1 | ENSG00000118855.21 | transcript | ENST00000415822.8 | protein_coding | 7/15 | chr3 | 158818359 | |||||||
| chr3:158818519 | C | A | 4 | a0001c0001t0001g0145 a0001c0001t0001g0146 a0001c0001t0001g0147 others(1): Show |
4 | HG02109.hp1 HG02145.hp1 HG02809.hp2 others(1): Show |
intron_variant | MODIFIER | c.653-1130C>A | MFSD1 | ENSG00000118855.21 | transcript | ENST00000415822.8 | protein_coding | 7/15 | chr3 | 158818519 | |||||||
| chr3:158818578 | AAT | A | 5 | a0002c0002t0001g0017 a0002c0002t0001g0240 a0002c0002t0001g0241 others(2): Show |
11 | HG01255.hp1 HG01884.hp2 HG02257.hp2 others(8): Show |
intron_variant | MODIFIER | c.653-1058_653-1057d others(4): Show |
MFSD1 | ENSG00000118855.21 | transcript | ENST00000415822.8 | protein_coding | 7/15 | INFO_REALIGN_3_PRIME | chr3 | 158818578 | ||||||
| chr3:158818592 | T | C | 20 | a0001c0001t0001g0016 a0001c0001t0001g0028 a0001c0001t0001g0029 others(17): Show |
36 | HG00140.hp1 HG00280.hp1 HG00639.hp2 others(33): Show |
intron_variant | MODIFIER | c.653-1057T>C | MFSD1 | ENSG00000118855.21 | transcript | ENST00000415822.8 | protein_coding | 7/15 | chr3 | 158818592 | |||||||
| chr3:158818653 | C | T | 1 | a0002c0002t0003g0019 | 3 | HG01243.hp1 HG02280.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.653-996C>T | MFSD1 | ENSG00000118855.21 | transcript | ENST00000415822.8 | protein_coding | 7/15 | chr3 | 158818653 | |||||||
| chr3:158818680 | G | A | 1 | a0001c0001t0001g0060 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.653-969G>A | MFSD1 | ENSG00000118855.21 | transcript | ENST00000415822.8 | protein_coding | 7/15 | chr3 | 158818680 | |||||||
| chr3:158818732 | C | T | 1 | a0001c0001t0001g0111 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.653-917C>T | MFSD1 | ENSG00000118855.21 | transcript | ENST00000415822.8 | protein_coding | 7/15 | chr3 | 158818732 | |||||||
| chr3:158818740 | A | G | 2 | a0002c0002t0001g0197 a0002c0002t0002g0195 |
2 | HG02109.hp2 HG02723.hp1 |
intron_variant | MODIFIER | c.653-909A>G | MFSD1 | ENSG00000118855.21 | transcript | ENST00000415822.8 | protein_coding | 7/15 | chr3 | 158818740 | |||||||
| chr3:158818764 | C | T | 4 | a0001c0001t0001g0145 a0001c0001t0001g0146 a0001c0001t0001g0147 others(1): Show |
4 | HG02109.hp1 HG02145.hp1 HG02809.hp2 others(1): Show |
intron_variant | MODIFIER | c.653-885C>T | MFSD1 | ENSG00000118855.21 | transcript | ENST00000415822.8 | protein_coding | 7/15 | chr3 | 158818764 | |||||||
| chr3:158818824 | A | G | 1 | a0003c0003t0001g0183 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.653-825A>G | MFSD1 | ENSG00000118855.21 | transcript | ENST00000415822.8 | protein_coding | 7/15 | chr3 | 158818824 | |||||||
| chr3:158818842 | C | A | 1 | a0002c0004t0001g0200 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.653-807C>A | MFSD1 | ENSG00000118855.21 | transcript | ENST00000415822.8 | protein_coding | 7/15 | chr3 | 158818842 | |||||||
| chr3:158818876 | C | T | 1 | a0001c0001t0001g0041 | 2 | HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.653-773C>T | MFSD1 | ENSG00000118855.21 | transcript | ENST00000415822.8 | protein_coding | 7/15 | chr3 | 158818876 | |||||||
| chr3:158819051 | C | A | 1 | a0002c0002t0001g0228 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.653-598C>A | MFSD1 | ENSG00000118855.21 | transcript | ENST00000415822.8 | protein_coding | 7/15 | chr3 | 158819051 | |||||||
| chr3:158819204 | C | T | 1 | a0002c0002t0001g0218 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.653-445C>T | MFSD1 | ENSG00000118855.21 | transcript | ENST00000415822.8 | protein_coding | 7/15 | chr3 | 158819204 | |||||||
| chr3:158819295 | A | G | 1 | a0002c0004t0001g0165 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.653-354A>G | MFSD1 | ENSG00000118855.21 | transcript | ENST00000415822.8 | protein_coding | 7/15 | chr3 | 158819295 | |||||||
| chr3:158819321 | T | C | 112 | a0001c0001t0001g0016 a0001c0001t0001g0026 a0001c0001t0001g0028 others(109): Show |
193 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(190): Show |
intron_variant | MODIFIER | c.653-328T>C | MFSD1 | ENSG00000118855.21 | transcript | ENST00000415822.8 | protein_coding | 7/15 | chr3 | 158819321 | |||||||
| chr3:158819380 | A | G | 3 | a0002c0004t0001g0163 a0002c0004t0001g0164 a0002c0004t0001g0165 |
3 | NA18975.hp2 NA19078.hp2 NA19091.hp1 |
intron_variant | MODIFIER | c.653-269A>G | MFSD1 | ENSG00000118855.21 | transcript | ENST00000415822.8 | protein_coding | 7/15 | chr3 | 158819380 | |||||||
| chr3:158819393 | T | G | 5 | a0001c0001t0001g0145 a0001c0001t0001g0146 a0001c0001t0001g0147 others(2): Show |
7 | HG01243.hp1 HG02109.hp1 HG02145.hp1 others(4): Show |
intron_variant | MODIFIER | c.653-256T>G | MFSD1 | ENSG00000118855.21 | transcript | ENST00000415822.8 | protein_coding | 7/15 | chr3 | 158819393 | |||||||
| chr3:158819430 | G | C | 3 | a0002c0002t0003g0020 a0002c0002t0003g0136 a0002c0002t0003g0137 |
5 | HG01891.hp1 HG02055.hp1 HG02622.hp2 others(2): Show |
intron_variant | MODIFIER | c.653-219G>C | MFSD1 | ENSG00000118855.21 | transcript | ENST00000415822.8 | protein_coding | 7/15 | chr3 | 158819430 | |||||||
| chr3:158819440 | G | A | 1 | a0002c0004t0001g0033 | 2 | NA18985.hp1 NA19075.hp1 |
intron_variant | MODIFIER | c.653-209G>A | MFSD1 | ENSG00000118855.21 | transcript | ENST00000415822.8 | protein_coding | 7/15 | chr3 | 158819440 | |||||||
| chr3:158819496 | C | G | 2 | a0002c0002t0005g0044 a0002c0002t0005g0143 |
3 | HG02622.hp1 HG03098.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.653-153C>G | MFSD1 | ENSG00000118855.21 | transcript | ENST00000415822.8 | protein_coding | 7/15 | chr3 | 158819496 | |||||||
| chr3:158819626 | CT | C | 110 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0007 others(107): Show |
163 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(160): Show |
splice_region_variant&intron_variant | LOW | c.653-7delT | MFSD1 | ENSG00000118855.21 | transcript | ENST00000415822.8 | protein_coding | 7/15 | INFO_REALIGN_3_PRIME | chr3 | 158819626 | ||||||
| chr3:158819626 | CTT | C | 8 | a0001c0001t0001g0078 a0001c0001t0001g0089 a0001c0001t0001g0090 others(5): Show |
8 | HG02109.hp1 HG02145.hp1 HG02809.hp2 others(5): Show |
splice_region_variant&intron_variant | LOW | c.653-8_653-7delTT | MFSD1 | ENSG00000118855.21 | transcript | ENST00000415822.8 | protein_coding | 7/15 | INFO_REALIGN_3_PRIME | chr3 | 158819626 | ||||||
| chr3:158819626 | CTTTTT | C | 118 | a0002c0002t0001g0008 a0002c0002t0001g0009 a0002c0002t0001g0013 others(115): Show |
221 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(218): Show |
splice_region_variant&intron_variant | LOW | c.653-11_653-7delTTT others(2): Show |
MFSD1 | ENSG00000118855.21 | transcript | ENST00000415822.8 | protein_coding | 7/15 | INFO_REALIGN_3_PRIME | chr3 | 158819626 | ||||||
| chr3:158819788 | C | T | 2 | a0002c0002t0005g0044 a0002c0002t0005g0143 |
3 | HG02622.hp1 HG03098.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.751+41C>T | MFSD1 | ENSG00000118855.21 | transcript | ENST00000415822.8 | protein_coding | 8/15 | chr3 | 158819788 | |||||||
| chr3:158820068 | A | T | 1 | a0002c0002t0001g0217 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.752-147A>T | MFSD1 | ENSG00000118855.21 | transcript | ENST00000415822.8 | protein_coding | 8/15 | chr3 | 158820068 | |||||||
| chr3:158820555 | T | C | 1 | a0001c0001t0004g0091 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.863+229T>C | MFSD1 | ENSG00000118855.21 | transcript | ENST00000415822.8 | protein_coding | 9/15 | chr3 | 158820555 | |||||||
| chr3:158820578 | A | G | 42 | a0001c0001t0008g0211 a0002c0002t0001g0013 a0002c0002t0001g0014 others(39): Show |
55 | HG00323.hp1 HG00639.hp1 HG00642.hp1 others(52): Show |
intron_variant | MODIFIER | c.863+252A>G | MFSD1 | ENSG00000118855.21 | transcript | ENST00000415822.8 | protein_coding | 9/15 | chr3 | 158820578 | |||||||
| chr3:158820614 | A | C | 3 | a0002c0004t0001g0163 a0002c0004t0001g0164 a0002c0004t0001g0165 |
3 | NA18975.hp2 NA19078.hp2 NA19091.hp1 |
intron_variant | MODIFIER | c.863+288A>C | MFSD1 | ENSG00000118855.21 | transcript | ENST00000415822.8 | protein_coding | 9/15 | chr3 | 158820614 | |||||||
| chr3:158820677 | A | G | 1 | a0002c0002t0010g0139 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.863+351A>G | MFSD1 | ENSG00000118855.21 | transcript | ENST00000415822.8 | protein_coding | 9/15 | chr3 | 158820677 | |||||||
| chr3:158820724 | C | T | 1 | a0002c0002t0001g0229 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.863+398C>T | MFSD1 | ENSG00000118855.21 | transcript | ENST00000415822.8 | protein_coding | 9/15 | chr3 | 158820724 | |||||||
| chr3:158820784 | C | T | 1 | a0003c0003t0002g0181 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.863+458C>T | MFSD1 | ENSG00000118855.21 | transcript | ENST00000415822.8 | protein_coding | 9/15 | chr3 | 158820784 | |||||||
| chr3:158820917 | AC | A | 5 | a0002c0002t0003g0015 a0002c0002t0003g0043 a0002c0002t0003g0140 others(2): Show |
9 | HG01255.hp1 HG02257.hp2 HG02451.hp1 others(6): Show |
intron_variant | MODIFIER | c.863+593delC | MFSD1 | ENSG00000118855.21 | transcript | ENST00000415822.8 | protein_coding | 9/15 | INFO_REALIGN_3_PRIME | chr3 | 158820917 | ||||||
| chr3:158820964 | A | G | 1 | a0002c0002t0001g0192 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.864-633A>G | MFSD1 | ENSG00000118855.21 | transcript | ENST00000415822.8 | protein_coding | 9/15 | chr3 | 158820964 | |||||||
| chr3:158821173 | C | CTGTT | 2 | a0002c0002t0003g0015 a0006c0009t0003g0224 |
5 | HG01255.hp1 HG02257.hp2 HG02451.hp1 others(2): Show |
intron_variant | MODIFIER | c.864-424_864-423ins others(4): Show |
MFSD1 | ENSG00000118855.21 | transcript | ENST00000415822.8 | protein_coding | 9/15 | chr3 | 158821173 | |||||||
| chr3:158821174 | G | T | 2 | a0002c0002t0003g0015 a0006c0009t0003g0224 |
5 | HG01255.hp1 HG02257.hp2 HG02451.hp1 others(2): Show |
intron_variant | MODIFIER | c.864-423G>T | MFSD1 | ENSG00000118855.21 | transcript | ENST00000415822.8 | protein_coding | 9/15 | chr3 | 158821174 | |||||||
| chr3:158821175 | C | T | 2 | a0002c0002t0003g0015 a0006c0009t0003g0224 |
5 | HG01255.hp1 HG02257.hp2 HG02451.hp1 others(2): Show |
intron_variant | MODIFIER | c.864-422C>T | MFSD1 | ENSG00000118855.21 | transcript | ENST00000415822.8 | protein_coding | 9/15 | chr3 | 158821175 | |||||||
| chr3:158821176 | A | T | 2 | a0002c0002t0003g0015 a0006c0009t0003g0224 |
5 | HG01255.hp1 HG02257.hp2 HG02451.hp1 others(2): Show |
intron_variant | MODIFIER | c.864-421A>T | MFSD1 | ENSG00000118855.21 | transcript | ENST00000415822.8 | protein_coding | 9/15 | chr3 | 158821176 | |||||||
| chr3:158821177 | A | G | 2 | a0002c0002t0003g0015 a0006c0009t0003g0224 |
5 | HG01255.hp1 HG02257.hp2 HG02451.hp1 others(2): Show |
intron_variant | MODIFIER | c.864-420A>G | MFSD1 | ENSG00000118855.21 | transcript | ENST00000415822.8 | protein_coding | 9/15 | chr3 | 158821177 | |||||||
| chr3:158821187 | G | T | 5 | a0002c0002t0003g0015 a0002c0002t0003g0043 a0002c0002t0003g0140 others(2): Show |
9 | HG01255.hp1 HG02257.hp2 HG02451.hp1 others(6): Show |
intron_variant | MODIFIER | c.864-410G>T | MFSD1 | ENSG00000118855.21 | transcript | ENST00000415822.8 | protein_coding | 9/15 | chr3 | 158821187 | |||||||
| chr3:158821320 | T | A | 1 | a0002c0008t0001g0221 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.864-277T>A | MFSD1 | ENSG00000118855.21 | transcript | ENST00000415822.8 | protein_coding | 9/15 | chr3 | 158821320 | |||||||
| chr3:158821477 | G | A | 12 | a0002c0002t0001g0008 a0002c0002t0001g0009 a0002c0002t0001g0017 others(9): Show |
27 | HG01074.hp1 HG01257.hp2 HG01258.hp2 others(24): Show |
intron_variant | MODIFIER | c.864-120G>A | MFSD1 | ENSG00000118855.21 | transcript | ENST00000415822.8 | protein_coding | 9/15 | chr3 | 158821477 | |||||||
| chr3:158821505 | G | A | 77 | a0001c0001t0008g0211 a0001c0007t0001g0161 a0002c0002t0001g0008 others(74): Show |
135 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(132): Show |
intron_variant | MODIFIER | c.864-92G>A | MFSD1 | ENSG00000118855.21 | transcript | ENST00000415822.8 | protein_coding | 9/15 | chr3 | 158821505 | |||||||
| chr3:158821697 | A | G | 52 | a0001c0001t0008g0211 a0002c0002t0001g0008 a0002c0002t0001g0009 others(49): Show |
80 | HG00639.hp1 HG00642.hp1 HG00642.hp2 others(77): Show |
intron_variant | MODIFIER | c.920+44A>G | MFSD1 | ENSG00000118855.21 | transcript | ENST00000415822.8 | protein_coding | 10/15 | chr3 | 158821697 | |||||||
| chr3:158821707 | A | G | 23 | a0001c0007t0001g0161 a0002c0004t0001g0001 a0002c0004t0001g0006 others(20): Show |
53 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(50): Show |
intron_variant | MODIFIER | c.920+54A>G | MFSD1 | ENSG00000118855.21 | transcript | ENST00000415822.8 | protein_coding | 10/15 | chr3 | 158821707 | |||||||
| chr3:158821755 | T | C | 1 | a0003c0003t0001g0049 | 2 | HG01106.hp2 HG01168.hp1 |
intron_variant | MODIFIER | c.920+102T>C | MFSD1 | ENSG00000118855.21 | transcript | ENST00000415822.8 | protein_coding | 10/15 | chr3 | 158821755 | |||||||
| chr3:158821853 | T | A | 1 | a0002c0004t0001g0200 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.921-131T>A | MFSD1 | ENSG00000118855.21 | transcript | ENST00000415822.8 | protein_coding | 10/15 | chr3 | 158821853 | |||||||
| chr3:158821950 | A | G | 2 | a0001c0007t0001g0161 a0002c0004t0001g0156 |
2 | HG00140.hp2 HG01261.hp2 |
intron_variant | MODIFIER | c.921-34A>G | MFSD1 | ENSG00000118855.21 | transcript | ENST00000415822.8 | protein_coding | 10/15 | chr3 | 158821950 | |||||||
| chr3:158821968 | T | C | 1 | a0001c0001t0001g0132 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.921-16T>C | MFSD1 | ENSG00000118855.21 | transcript | ENST00000415822.8 | protein_coding | 10/15 | chr3 | 158821968 | |||||||
| chr3:158822145 | C | T | 5 | a0001c0001t0001g0039 a0001c0001t0001g0108 a0001c0001t0001g0109 others(2): Show |
6 | HG01346.hp2 HG01496.hp1 HG01978.hp2 others(3): Show |
splice_region_variant&intron_variant | LOW | c.1077+5C>T | MFSD1 | ENSG00000118855.21 | transcript | ENST00000415822.8 | protein_coding | 11/15 | chr3 | 158822145 | |||||||
| chr3:158822172 | G | A | 51 | a0001c0001t0008g0211 a0002c0002t0001g0008 a0002c0002t0001g0009 others(48): Show |
79 | HG00639.hp1 HG00642.hp1 HG00642.hp2 others(76): Show |
intron_variant | MODIFIER | c.1077+32G>A | MFSD1 | ENSG00000118855.21 | transcript | ENST00000415822.8 | protein_coding | 11/15 | chr3 | 158822172 | |||||||
| chr3:158822214 | G | A | 2 | a0003c0003t0002g0170 a0003c0003t0002g0185 |
2 | HG02559.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.1077+74G>A | MFSD1 | ENSG00000118855.21 | transcript | ENST00000415822.8 | protein_coding | 11/15 | chr3 | 158822214 | |||||||
| chr3:158822448 | G | A | 75 | a0001c0001t0008g0211 a0001c0007t0001g0161 a0002c0002t0001g0008 others(72): Show |
133 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(130): Show |
intron_variant | MODIFIER | c.1077+308G>A | MFSD1 | ENSG00000118855.21 | transcript | ENST00000415822.8 | protein_coding | 11/15 | chr3 | 158822448 | |||||||
| chr3:158822502 | G | T | 39 | a0001c0001t0008g0211 a0002c0002t0001g0013 a0002c0002t0001g0014 others(36): Show |
52 | HG00639.hp1 HG00642.hp1 HG00642.hp2 others(49): Show |
intron_variant | MODIFIER | c.1077+362G>T | MFSD1 | ENSG00000118855.21 | transcript | ENST00000415822.8 | protein_coding | 11/15 | chr3 | 158822502 | |||||||
| chr3:158822577 | G | A | 23 | a0001c0007t0001g0161 a0002c0004t0001g0001 a0002c0004t0001g0006 others(20): Show |
53 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(50): Show |
intron_variant | MODIFIER | c.1077+437G>A | MFSD1 | ENSG00000118855.21 | transcript | ENST00000415822.8 | protein_coding | 11/15 | chr3 | 158822577 | |||||||
| chr3:158822789 | C | T | 1 | a0002c0004t0001g0141 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.1078-639C>T | MFSD1 | ENSG00000118855.21 | transcript | ENST00000415822.8 | protein_coding | 11/15 | chr3 | 158822789 | |||||||
| chr3:158822845 | A | G | 1 | a0001c0001t0001g0107 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.1078-583A>G | MFSD1 | ENSG00000118855.21 | transcript | ENST00000415822.8 | protein_coding | 11/15 | chr3 | 158822845 | |||||||
| chr3:158822953 | A | T | 3 | a0001c0001t0001g0226 a0001c0001t0001g0231 a0001c0001t0001g0237 |
3 | HG01167.hp2 HG03041.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.1078-475A>T | MFSD1 | ENSG00000118855.21 | transcript | ENST00000415822.8 | protein_coding | 11/15 | chr3 | 158822953 | |||||||
| chr3:158822983 | C | T | 1 | a0001c0001t0001g0112 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.1078-445C>T | MFSD1 | ENSG00000118855.21 | transcript | ENST00000415822.8 | protein_coding | 11/15 | chr3 | 158822983 | |||||||
| chr3:158823019 | G | T | 1 | a0002c0004t0001g0155 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.1078-409G>T | MFSD1 | ENSG00000118855.21 | transcript | ENST00000415822.8 | protein_coding | 11/15 | chr3 | 158823019 | |||||||
| chr3:158823113 | A | G | 23 | a0001c0007t0001g0161 a0002c0004t0001g0001 a0002c0004t0001g0006 others(20): Show |
53 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(50): Show |
intron_variant | MODIFIER | c.1078-315A>G | MFSD1 | ENSG00000118855.21 | transcript | ENST00000415822.8 | protein_coding | 11/15 | chr3 | 158823113 | |||||||
| chr3:158823172 | C | T | 3 | a0002c0002t0001g0014 a0002c0002t0001g0215 a0002c0002t0001g0220 |
6 | HG00642.hp2 HG01099.hp2 HG01106.hp1 others(3): Show |
intron_variant | MODIFIER | c.1078-256C>T | MFSD1 | ENSG00000118855.21 | transcript | ENST00000415822.8 | protein_coding | 11/15 | chr3 | 158823172 | |||||||
| chr3:158823192 | A | G | 3 | a0004c0005t0001g0023 a0004c0005t0001g0199 a0004c0005t0001g0210 |
5 | HG01175.hp1 HG02486.hp2 HG02630.hp2 others(2): Show |
intron_variant | MODIFIER | c.1078-236A>G | MFSD1 | ENSG00000118855.21 | transcript | ENST00000415822.8 | protein_coding | 11/15 | chr3 | 158823192 | |||||||
| chr3:158823288 | C | T | 11 | a0002c0002t0001g0138 a0002c0002t0010g0139 a0003c0003t0002g0002 others(8): Show |
31 | HG00280.hp1 HG01070.hp1 HG01071.hp2 others(28): Show |
intron_variant | MODIFIER | c.1078-140C>T | MFSD1 | ENSG00000118855.21 | transcript | ENST00000415822.8 | protein_coding | 11/15 | chr3 | 158823288 | |||||||
| chr3:158823413 | C | A | 1 | a0001c0001t0001g0041 | 2 | HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.1078-15C>A | MFSD1 | ENSG00000118855.21 | transcript | ENST00000415822.8 | protein_coding | 11/15 | chr3 | 158823413 | |||||||
| chr3:158823537 | C | T | 1 | a0001c0001t0001g0088 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.1175+12C>T | MFSD1 | ENSG00000118855.21 | transcript | ENST00000415822.8 | protein_coding | 12/15 | chr3 | 158823537 | |||||||
| chr3:158823808 | T | C | 23 | a0001c0007t0001g0161 a0002c0004t0001g0001 a0002c0004t0001g0006 others(20): Show |
53 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(50): Show |
intron_variant | MODIFIER | c.1175+283T>C | MFSD1 | ENSG00000118855.21 | transcript | ENST00000415822.8 | protein_coding | 12/15 | chr3 | 158823808 | |||||||
| chr3:158823873 | C | G | 1 | a0002c0004t0001g0200 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1176-251C>G | MFSD1 | ENSG00000118855.21 | transcript | ENST00000415822.8 | protein_coding | 12/15 | chr3 | 158823873 | |||||||
| chr3:158824015 | G | C | 3 | a0001c0001t0001g0079 a0001c0001t0001g0092 a0001c0001t0001g0093 |
3 | HG03491.hp2 HG03492.hp1 HG04115.hp2 |
intron_variant | MODIFIER | c.1176-109G>C | MFSD1 | ENSG00000118855.21 | transcript | ENST00000415822.8 | protein_coding | 12/15 | chr3 | 158824015 | |||||||
| chr3:158824070 | T | C | 1 | a0003c0003t0002g0171 | 1 | NA19056.hp2 | intron_variant | MODIFIER | c.1176-54T>C | MFSD1 | ENSG00000118855.21 | transcript | ENST00000415822.8 | protein_coding | 12/15 | chr3 | 158824070 | |||||||
| chr3:158824102 | C | T | 1 | a0002c0004t0001g0141 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.1176-22C>T | MFSD1 | ENSG00000118855.21 | transcript | ENST00000415822.8 | protein_coding | 12/15 | chr3 | 158824102 | |||||||
| chr3:158824460 | C | A | 1 | a0001c0001t0001g0112 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.1288+224C>A | MFSD1 | ENSG00000118855.21 | transcript | ENST00000415822.8 | protein_coding | 13/15 | chr3 | 158824460 | |||||||
| chr3:158824521 | T | C | 1 | a0001c0001t0001g0094 | 1 | NA19080.hp2 | intron_variant | MODIFIER | c.1288+285T>C | MFSD1 | ENSG00000118855.21 | transcript | ENST00000415822.8 | protein_coding | 13/15 | chr3 | 158824521 | |||||||
| chr3:158824788 | G | C | 23 | a0001c0007t0001g0161 a0002c0004t0001g0001 a0002c0004t0001g0006 others(20): Show |
53 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(50): Show |
intron_variant | MODIFIER | c.1288+552G>C | MFSD1 | ENSG00000118855.21 | transcript | ENST00000415822.8 | protein_coding | 13/15 | chr3 | 158824788 | |||||||
| chr3:158824842 | T | A | 5 | a0002c0002t0001g0027 a0002c0002t0001g0227 a0002c0002t0001g0228 others(2): Show |
9 | HG00280.hp1 HG00735.hp2 HG00741.hp2 others(6): Show |
intron_variant | MODIFIER | c.1288+606T>A | MFSD1 | ENSG00000118855.21 | transcript | ENST00000415822.8 | protein_coding | 13/15 | chr3 | 158824842 | |||||||
| chr3:158824885 | G | A | 5 | a0001c0001t0001g0059 a0001c0001t0001g0095 a0001c0001t0001g0096 others(2): Show |
5 | HG02074.hp2 NA18747.hp1 NA18983.hp2 others(2): Show |
intron_variant | MODIFIER | c.1288+649G>A | MFSD1 | ENSG00000118855.21 | transcript | ENST00000415822.8 | protein_coding | 13/15 | chr3 | 158824885 | |||||||
| chr3:158824945 | C | T | 1 | a0002c0002t0002g0195 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.1288+709C>T | MFSD1 | ENSG00000118855.21 | transcript | ENST00000415822.8 | protein_coding | 13/15 | chr3 | 158824945 | |||||||
| chr3:158824958 | G | C | 3 | a0002c0004t0001g0163 a0002c0004t0001g0164 a0002c0004t0001g0165 |
3 | NA18975.hp2 NA19078.hp2 NA19091.hp1 |
intron_variant | MODIFIER | c.1288+722G>C | MFSD1 | ENSG00000118855.21 | transcript | ENST00000415822.8 | protein_coding | 13/15 | chr3 | 158824958 | |||||||
| chr3:158825020 | G | A | 70 | a0001c0007t0001g0161 a0002c0002t0001g0027 a0002c0002t0001g0057 others(67): Show |
145 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(142): Show |
intron_variant | MODIFIER | c.1288+784G>A | MFSD1 | ENSG00000118855.21 | transcript | ENST00000415822.8 | protein_coding | 13/15 | chr3 | 158825020 | |||||||
| chr3:158825234 | A | G | 3 | a0002c0002t0003g0020 a0002c0002t0003g0136 a0002c0002t0003g0137 |
5 | HG01891.hp1 HG02055.hp1 HG02622.hp2 others(2): Show |
intron_variant | MODIFIER | c.1289-781A>G | MFSD1 | ENSG00000118855.21 | transcript | ENST00000415822.8 | protein_coding | 13/15 | chr3 | 158825234 | |||||||
| chr3:158825309 | C | T | 1 | a0002c0004t0001g0200 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1289-706C>T | MFSD1 | ENSG00000118855.21 | transcript | ENST00000415822.8 | protein_coding | 13/15 | chr3 | 158825309 | |||||||
| chr3:158825351 | T | G | 11 | a0002c0002t0001g0138 a0002c0002t0003g0015 a0002c0002t0003g0043 others(8): Show |
16 | HG01243.hp2 HG01255.hp1 HG01433.hp2 others(13): Show |
intron_variant | MODIFIER | c.1289-664T>G | MFSD1 | ENSG00000118855.21 | transcript | ENST00000415822.8 | protein_coding | 13/15 | chr3 | 158825351 | |||||||
| chr3:158825524 | A | G | 1 | a0002c0004t0001g0165 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.1289-491A>G | MFSD1 | ENSG00000118855.21 | transcript | ENST00000415822.8 | protein_coding | 13/15 | chr3 | 158825524 | |||||||
| chr3:158825811 | T | C | 3 | a0002c0004t0001g0163 a0002c0004t0001g0164 a0002c0004t0001g0165 |
3 | NA18975.hp2 NA19078.hp2 NA19091.hp1 |
intron_variant | MODIFIER | c.1289-204T>C | MFSD1 | ENSG00000118855.21 | transcript | ENST00000415822.8 | protein_coding | 13/15 | chr3 | 158825811 | |||||||
| chr3:158825913 | A | G | 2 | a0001c0001t0001g0072 a0001c0001t0001g0131 |
2 | HG02056.hp1 HG02155.hp2 |
intron_variant | MODIFIER | c.1289-102A>G | MFSD1 | ENSG00000118855.21 | transcript | ENST00000415822.8 | protein_coding | 13/15 | chr3 | 158825913 | |||||||
| chr3:158826068 | T | C | 1 | a0002c0002t0001g0220 | 1 | HG00642.hp2 | splice_region_variant&intron_variant | LOW | c.1336+6T>C | MFSD1 | ENSG00000118855.21 | transcript | ENST00000415822.8 | protein_coding | 14/15 | chr3 | 158826068 | |||||||
| chr3:158826095 | C | T | 1 | a0002c0002t0001g0009 | 5 | HG02080.hp1 NA18967.hp2 NA18982.hp1 others(2): Show |
intron_variant | MODIFIER | c.1336+33C>T | MFSD1 | ENSG00000118855.21 | transcript | ENST00000415822.8 | protein_coding | 14/15 | chr3 | 158826095 | |||||||
| chr3:158826097 | G | A | 1 | a0002c0004t0001g0141 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.1336+35G>A | MFSD1 | ENSG00000118855.21 | transcript | ENST00000415822.8 | protein_coding | 14/15 | chr3 | 158826097 | |||||||
| chr3:158826233 | T | C | 1 | a0001c0001t0001g0223 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.1336+171T>C | MFSD1 | ENSG00000118855.21 | transcript | ENST00000415822.8 | protein_coding | 14/15 | chr3 | 158826233 | |||||||
| chr3:158826381 | G | A | 122 | a0001c0001t0008g0211 a0001c0007t0001g0161 a0002c0002t0001g0008 others(119): Show |
225 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(222): Show |
intron_variant | MODIFIER | c.1336+319G>A | MFSD1 | ENSG00000118855.21 | transcript | ENST00000415822.8 | protein_coding | 14/15 | chr3 | 158826381 | |||||||
| chr3:158826547 | A | G | 78 | a0001c0001t0001g0010 a0001c0001t0001g0061 a0001c0001t0006g0010 others(75): Show |
138 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(135): Show |
intron_variant | MODIFIER | c.1336+485A>G | MFSD1 | ENSG00000118855.21 | transcript | ENST00000415822.8 | protein_coding | 14/15 | chr3 | 158826547 | |||||||
| chr3:158826730 | C | T | 1 | a0002c0002t0001g0209 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.1337-550C>T | MFSD1 | ENSG00000118855.21 | transcript | ENST00000415822.8 | protein_coding | 14/15 | chr3 | 158826730 | |||||||
| chr3:158826885 | T | C | 2 | a0002c0002t0001g0138 a0002c0002t0010g0139 |
2 | HG01243.hp2 HG01433.hp2 |
intron_variant | MODIFIER | c.1337-395T>C | MFSD1 | ENSG00000118855.21 | transcript | ENST00000415822.8 | protein_coding | 14/15 | chr3 | 158826885 | |||||||
| chr3:158826933 | C | T | 19 | a0001c0007t0001g0161 a0002c0004t0001g0001 a0002c0004t0001g0006 others(16): Show |
49 | HG00099.hp1 HG00140.hp2 HG00733.hp1 others(46): Show |
intron_variant | MODIFIER | c.1337-347C>T | MFSD1 | ENSG00000118855.21 | transcript | ENST00000415822.8 | protein_coding | 14/15 | chr3 | 158826933 | |||||||
| chr3:158827118 | A | G | 15 | a0001c0001t0001g0010 a0001c0001t0001g0061 a0001c0001t0006g0010 others(12): Show |
32 | HG00408.hp1 HG00558.hp2 HG01074.hp1 others(29): Show |
intron_variant | MODIFIER | c.1337-162A>G | MFSD1 | ENSG00000118855.21 | transcript | ENST00000415822.8 | protein_coding | 14/15 | chr3 | 158827118 | |||||||
| chr3:158827196 | A | G | 1 | a0002c0002t0001g0218 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.1337-84A>G | MFSD1 | ENSG00000118855.21 | transcript | ENST00000415822.8 | protein_coding | 14/15 | chr3 | 158827196 | |||||||
| chr3:158827271 | G | C | 1 | a0001c0001t0001g0098 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.1337-9G>C | MFSD1 | ENSG00000118855.21 | transcript | ENST00000415822.8 | protein_coding | 14/15 | chr3 | 158827271 | |||||||
| chr3:158827406 | G | T | 55 | a0001c0001t0001g0010 a0001c0001t0001g0061 a0001c0001t0006g0010 others(52): Show |
85 | HG00408.hp1 HG00558.hp2 HG00639.hp1 others(82): Show |
intron_variant | MODIFIER | c.1394+69G>T | MFSD1 | ENSG00000118855.21 | transcript | ENST00000415822.8 | protein_coding | 15/15 | chr3 | 158827406 | |||||||
| chr3:158827420 | G | GT | 34 | a0001c0001t0001g0038 a0001c0001t0001g0068 a0001c0001t0001g0071 others(31): Show |
66 | HG00140.hp2 HG00323.hp1 HG00609.hp2 others(63): Show |
intron_variant | MODIFIER | c.1394+100dupT | MFSD1 | ENSG00000118855.21 | transcript | ENST00000415822.8 | protein_coding | 15/15 | INFO_REALIGN_3_PRIME | chr3 | 158827420 | ||||||
| chr3:158827420 | G | GTT | 4 | a0002c0004t0001g0045 a0002c0004t0001g0055 a0002c0004t0001g0160 others(1): Show |
6 | HG00099.hp1 HG02738.hp2 HG03490.hp1 others(3): Show |
intron_variant | MODIFIER | c.1394+99_1394+100du others(3): Show |
MFSD1 | ENSG00000118855.21 | transcript | ENST00000415822.8 | protein_coding | 15/15 | INFO_REALIGN_3_PRIME | chr3 | 158827420 | ||||||
| chr3:158827420 | GT | G | 6 | a0001c0001t0001g0111 a0001c0001t0001g0122 a0002c0002t0001g0240 others(3): Show |
8 | HG01175.hp1 HG02258.hp2 HG02486.hp2 others(5): Show |
intron_variant | MODIFIER | c.1394+100delT | MFSD1 | ENSG00000118855.21 | transcript | ENST00000415822.8 | protein_coding | 15/15 | INFO_REALIGN_3_PRIME | chr3 | 158827420 | ||||||
| chr3:158827431 | T | G | 3 | a0004c0005t0001g0023 a0004c0005t0001g0199 a0004c0005t0001g0210 |
5 | HG01175.hp1 HG02486.hp2 HG02630.hp2 others(2): Show |
intron_variant | MODIFIER | c.1394+94T>G | MFSD1 | ENSG00000118855.21 | transcript | ENST00000415822.8 | protein_coding | 15/15 | chr3 | 158827431 | |||||||
| chr3:158827510 | G | A | 34 | a0001c0001t0001g0005 a0001c0001t0001g0011 a0001c0001t0001g0031 others(31): Show |
48 | HG00408.hp2 HG00423.hp1 HG00558.hp1 others(45): Show |
intron_variant | MODIFIER | c.1394+173G>A | MFSD1 | ENSG00000118855.21 | transcript | ENST00000415822.8 | protein_coding | 15/15 | chr3 | 158827510 | |||||||
| chr3:158827651 | A | G | 1 | a0002c0004t0001g0200 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1394+314A>G | MFSD1 | ENSG00000118855.21 | transcript | ENST00000415822.8 | protein_coding | 15/15 | chr3 | 158827651 | |||||||
| chr3:158827708 | G | C | 1 | a0002c0004t0001g0165 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.1394+371G>C | MFSD1 | ENSG00000118855.21 | transcript | ENST00000415822.8 | protein_coding | 15/15 | chr3 | 158827708 | |||||||
| chr3:158827843 | A | G | 45 | a0002c0002t0001g0027 a0002c0002t0001g0057 a0002c0002t0001g0227 others(42): Show |
90 | HG00280.hp1 HG00423.hp2 HG00609.hp2 others(87): Show |
intron_variant | MODIFIER | c.1394+506A>G | MFSD1 | ENSG00000118855.21 | transcript | ENST00000415822.8 | protein_coding | 15/15 | chr3 | 158827843 | |||||||
| chr3:158827898 | CAG | C | 13 | a0002c0002t0002g0195 a0002c0002t0003g0015 a0002c0002t0003g0019 others(10): Show |
22 | HG01069.hp2 HG01243.hp1 HG01255.hp1 others(19): Show |
intron_variant | MODIFIER | c.1394+574_1394+575d others(4): Show |
MFSD1 | ENSG00000118855.21 | transcript | ENST00000415822.8 | protein_coding | 15/15 | INFO_REALIGN_3_PRIME | chr3 | 158827898 | ||||||
| chr3:158827898 | CAGAGAGA others(25): Show |
C | 29 | a0002c0002t0001g0027 a0002c0002t0001g0057 a0002c0002t0001g0227 others(26): Show |
65 | HG00280.hp1 HG00423.hp2 HG00609.hp2 others(62): Show |
intron_variant | MODIFIER | c.1394+574_1394+605d others(34): Show |
MFSD1 | ENSG00000118855.21 | transcript | ENST00000415822.8 | protein_coding | 15/15 | INFO_REALIGN_3_PRIME | chr3 | 158827898 | ||||||
| chr3:158827909 | AGAGGGGG others(27): Show |
A | 1 | a0002c0002t0003g0140 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.1394+574_1394+607d others(36): Show |
MFSD1 | ENSG00000118855.21 | transcript | ENST00000415822.8 | protein_coding | 15/15 | INFO_REALIGN_3_PRIME | chr3 | 158827909 | ||||||
| chr3:158827910 | GAGGGGGA others(24): Show |
G | 1 | a0003c0003t0002g0174 | 1 | NA18985.hp2 | intron_variant | MODIFIER | c.1394+574_1394+604d others(33): Show |
MFSD1 | ENSG00000118855.21 | transcript | ENST00000415822.8 | protein_coding | 15/15 | chr3 | 158827910 | |||||||
| chr3:158827911 | A | G | 9 | a0001c0001t0001g0059 a0001c0001t0001g0095 a0001c0001t0001g0096 others(6): Show |
9 | HG02074.hp2 HG03239.hp2 NA18747.hp1 others(6): Show |
intron_variant | MODIFIER | c.1394+574A>G | MFSD1 | ENSG00000118855.21 | transcript | ENST00000415822.8 | protein_coding | 15/15 | chr3 | 158827911 | |||||||
| chr3:158827915 | G | A | 7 | a0001c0001t0001g0059 a0001c0001t0001g0095 a0001c0001t0001g0096 others(4): Show |
7 | HG02074.hp2 HG02647.hp1 HG03239.hp2 others(4): Show |
intron_variant | MODIFIER | c.1394+578G>A | MFSD1 | ENSG00000118855.21 | transcript | ENST00000415822.8 | protein_coding | 15/15 | chr3 | 158827915 | |||||||
| chr3:158827915 | G | GAGAGAGA | 4 | a0001c0001t0001g0003 a0001c0001t0001g0011 a0001c0001t0001g0151 others(1): Show |
4 | HG01109.hp1 NA18948.hp1 NA18957.hp2 others(1): Show |
intron_variant | MODIFIER | c.1394+578_1394+579i others(9): Show |
MFSD1 | ENSG00000118855.21 | transcript | ENST00000415822.8 | protein_coding | 15/15 | chr3 | 158827915 | |||||||
| chr3:158827915 | G | GAGAGAGA others(4): Show |
1 | a0001c0001t0001g0073 | 1 | NA19064.hp2 | intron_variant | MODIFIER | c.1394+578_1394+579i others(13): Show |
MFSD1 | ENSG00000118855.21 | transcript | ENST00000415822.8 | protein_coding | 15/15 | chr3 | 158827915 | |||||||
| chr3:158827915 | G | GAGAGAGA others(10): Show |
1 | a0001c0001t0001g0132 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.1394+578_1394+579i others(19): Show |
MFSD1 | ENSG00000118855.21 | transcript | ENST00000415822.8 | protein_coding | 15/15 | chr3 | 158827915 | |||||||
| chr3:158827915 | G | GGAGAGAG others(3): Show |
1 | a0001c0001t0001g0145 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.1394+596_1394+605d others(12): Show |
MFSD1 | ENSG00000118855.21 | transcript | ENST00000415822.8 | protein_coding | 15/15 | INFO_REALIGN_3_PRIME | chr3 | 158827915 | ||||||
| chr3:158827915 | G | GGAGAGAG others(13): Show |
1 | a0001c0001t0001g0036 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.1394+586_1394+605d others(22): Show |
MFSD1 | ENSG00000118855.21 | transcript | ENST00000415822.8 | protein_coding | 15/15 | INFO_REALIGN_3_PRIME | chr3 | 158827915 | ||||||
| chr3:158827915 | G | GGGAGAGA others(4): Show |
1 | a0002c0002t0001g0216 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.1394+579_1394+580i others(13): Show |
MFSD1 | ENSG00000118855.21 | transcript | ENST00000415822.8 | protein_coding | 15/15 | INFO_REALIGN_3_PRIME | chr3 | 158827915 | ||||||
| chr3:158827915 | G | GGGAGAGA others(6): Show |
2 | a0002c0002t0001g0013 a0004c0005t0001g0023 |
2 | HG02486.hp2 HG02630.hp1 |
intron_variant | MODIFIER | c.1394+579_1394+580i others(15): Show |
MFSD1 | ENSG00000118855.21 | transcript | ENST00000415822.8 | protein_coding | 15/15 | INFO_REALIGN_3_PRIME | chr3 | 158827915 | ||||||
| chr3:158827915 | G | GGGGA | 4 | a0002c0002t0001g0008 a0002c0002t0001g0009 a0002c0002t0001g0053 others(1): Show |
8 | HG01361.hp2 HG02027.hp2 HG02280.hp1 others(5): Show |
intron_variant | MODIFIER | c.1394+579_1394+580i others(6): Show |
MFSD1 | ENSG00000118855.21 | transcript | ENST00000415822.8 | protein_coding | 15/15 | INFO_REALIGN_3_PRIME | chr3 | 158827915 | ||||||
| chr3:158827915 | G | GGGGAGAG others(3): Show |
2 | a0002c0002t0001g0008 a0002c0002t0001g0054 |
4 | HG01257.hp2 HG01258.hp2 HG03491.hp1 others(1): Show |
intron_variant | MODIFIER | c.1394+579_1394+580i others(12): Show |
MFSD1 | ENSG00000118855.21 | transcript | ENST00000415822.8 | protein_coding | 15/15 | INFO_REALIGN_3_PRIME | chr3 | 158827915 | ||||||
| chr3:158827915 | G | GGGGAGAG others(5): Show |
3 | a0001c0001t0001g0010 a0001c0001t0001g0061 a0001c0001t0006g0010 |
3 | HG00408.hp1 HG00558.hp2 HG02523.hp2 |
intron_variant | MODIFIER | c.1394+579_1394+580i others(14): Show |
MFSD1 | ENSG00000118855.21 | transcript | ENST00000415822.8 | protein_coding | 15/15 | INFO_REALIGN_3_PRIME | chr3 | 158827915 | ||||||
| chr3:158827915 | G | GGGGAGAG others(7): Show |
1 | a0001c0001t0001g0010 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.1394+579_1394+580i others(16): Show |
MFSD1 | ENSG00000118855.21 | transcript | ENST00000415822.8 | protein_coding | 15/15 | INFO_REALIGN_3_PRIME | chr3 | 158827915 | ||||||
| chr3:158827915 | G | GGGGAGAG others(15): Show |
1 | a0002c0002t0001g0024 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.1394+579_1394+580i others(24): Show |
MFSD1 | ENSG00000118855.21 | transcript | ENST00000415822.8 | protein_coding | 15/15 | INFO_REALIGN_3_PRIME | chr3 | 158827915 | ||||||
| chr3:158827915 | GGAGAGAG others(25): Show |
G | 1 | a0002c0004t0001g0055 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.1394+606_1394+637d others(34): Show |
MFSD1 | ENSG00000118855.21 | transcript | ENST00000415822.8 | protein_coding | 15/15 | INFO_REALIGN_3_PRIME | chr3 | 158827915 | ||||||
| chr3:158827916 | GA | G | 5 | a0001c0001t0001g0003 a0002c0002t0001g0220 a0002c0002t0001g0241 others(2): Show |
6 | HG00642.hp2 HG03209.hp2 HG04199.hp2 others(3): Show |
intron_variant | MODIFIER | c.1394+580delA | MFSD1 | ENSG00000118855.21 | transcript | ENST00000415822.8 | protein_coding | 15/15 | chr3 | 158827916 | |||||||
| chr3:158827917 | A | G | 6 | a0001c0001t0001g0100 a0002c0002t0001g0017 a0002c0002t0001g0138 others(3): Show |
8 | HG01243.hp2 HG01433.hp2 HG01884.hp2 others(5): Show |
intron_variant | MODIFIER | c.1394+580A>G | MFSD1 | ENSG00000118855.21 | transcript | ENST00000415822.8 | protein_coding | 15/15 | chr3 | 158827917 | |||||||
| chr3:158827917 | AGAGAGAG others(21): Show |
A | 11 | a0002c0002t0002g0195 a0002c0002t0003g0019 a0002c0002t0003g0020 others(8): Show |
14 | HG01069.hp2 HG01243.hp1 HG01891.hp1 others(11): Show |
intron_variant | MODIFIER | c.1394+606_1394+633d others(30): Show |
MFSD1 | ENSG00000118855.21 | transcript | ENST00000415822.8 | protein_coding | 15/15 | INFO_REALIGN_3_PRIME | chr3 | 158827917 | ||||||
| chr3:158827919 | A | G | 1 | a0002c0002t0001g0241 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.1394+582A>G | MFSD1 | ENSG00000118855.21 | transcript | ENST00000415822.8 | protein_coding | 15/15 | chr3 | 158827919 | |||||||
| chr3:158827919 | AGAGAGAG others(19): Show |
A | 24 | a0001c0007t0001g0161 a0002c0002t0003g0019 a0002c0002t0003g0020 others(21): Show |
48 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(45): Show |
intron_variant | MODIFIER | c.1394+606_1394+631d others(28): Show |
MFSD1 | ENSG00000118855.21 | transcript | ENST00000415822.8 | protein_coding | 15/15 | INFO_REALIGN_3_PRIME | chr3 | 158827919 | ||||||
| chr3:158827921 | AGAGAGAG others(17): Show |
A | 6 | a0002c0002t0003g0015 a0002c0002t0003g0043 a0002c0004t0001g0001 others(3): Show |
10 | HG01255.hp1 HG02451.hp1 HG02723.hp2 others(7): Show |
intron_variant | MODIFIER | c.1394+606_1394+629d others(26): Show |
MFSD1 | ENSG00000118855.21 | transcript | ENST00000415822.8 | protein_coding | 15/15 | INFO_REALIGN_3_PRIME | chr3 | 158827921 | ||||||
| chr3:158827927 | AGAGAGAG others(11): Show |
A | 1 | a0002c0002t0001g0219 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1394+606_1394+623d others(20): Show |
MFSD1 | ENSG00000118855.21 | transcript | ENST00000415822.8 | protein_coding | 15/15 | INFO_REALIGN_3_PRIME | chr3 | 158827927 | ||||||
| chr3:158827929 | AGAGAGAG others(9): Show |
A | 3 | a0002c0002t0001g0138 a0002c0002t0001g0198 a0002c0002t0010g0139 |
3 | HG01243.hp2 HG01433.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.1394+606_1394+621d others(18): Show |
MFSD1 | ENSG00000118855.21 | transcript | ENST00000415822.8 | protein_coding | 15/15 | INFO_REALIGN_3_PRIME | chr3 | 158827929 | ||||||
| chr3:158827931 | AGAGAGAG others(7): Show |
A | 3 | a0001c0001t0001g0223 a0001c0001t0001g0234 a0003c0003t0001g0183 |
3 | HG02647.hp2 HG02922.hp1 HG04204.hp2 |
intron_variant | MODIFIER | c.1394+606_1394+619d others(16): Show |
MFSD1 | ENSG00000118855.21 | transcript | ENST00000415822.8 | protein_coding | 15/15 | INFO_REALIGN_3_PRIME | chr3 | 158827931 | ||||||
| chr3:158827933 | AGAGAGAG others(5): Show |
A | 3 | a0001c0001t0001g0026 a0002c0004t0001g0163 a0002c0004t0001g0164 |
3 | HG03209.hp1 NA18975.hp2 NA19091.hp1 |
intron_variant | MODIFIER | c.1394+606_1394+617d others(14): Show |
MFSD1 | ENSG00000118855.21 | transcript | ENST00000415822.8 | protein_coding | 15/15 | INFO_REALIGN_3_PRIME | chr3 | 158827933 | ||||||
| chr3:158827935 | A | AGAGGAGG others(31): Show |
1 | a0001c0001t0001g0105 | 1 | NA18972.hp2 | intron_variant | MODIFIER | c.1394+601_1394+602i others(40): Show |
MFSD1 | ENSG00000118855.21 | transcript | ENST00000415822.8 | protein_coding | 15/15 | INFO_REALIGN_3_PRIME | chr3 | 158827935 | ||||||
| chr3:158827935 | AGAGAGAG others(3): Show |
A | 4 | a0001c0001t0001g0030 a0002c0002t0001g0014 a0002c0004t0001g0165 others(1): Show |
5 | HG01106.hp2 HG01168.hp1 HG02976.hp2 others(2): Show |
intron_variant | MODIFIER | c.1394+606_1394+615d others(12): Show |
MFSD1 | ENSG00000118855.21 | transcript | ENST00000415822.8 | protein_coding | 15/15 | INFO_REALIGN_3_PRIME | chr3 | 158827935 | ||||||
| chr3:158827937 | AGAGAGGG others(1): Show |
A | 6 | a0001c0001t0001g0003 a0001c0001t0001g0026 a0001c0001t0001g0029 others(3): Show |
8 | HG01884.hp1 HG02129.hp1 HG02145.hp2 others(5): Show |
intron_variant | MODIFIER | c.1394+606_1394+613d others(10): Show |
MFSD1 | ENSG00000118855.21 | transcript | ENST00000415822.8 | protein_coding | 15/15 | INFO_REALIGN_3_PRIME | chr3 | 158827937 | ||||||
| chr3:158827939 | AGAGGGG | A | 6 | a0001c0001t0001g0003 a0001c0001t0001g0042 a0001c0001t0012g0084 others(3): Show |
7 | HG02132.hp2 HG02451.hp2 HG03453.hp1 others(4): Show |
intron_variant | MODIFIER | c.1394+606_1394+611d others(8): Show |
MFSD1 | ENSG00000118855.21 | transcript | ENST00000415822.8 | protein_coding | 15/15 | INFO_REALIGN_3_PRIME | chr3 | 158827939 | ||||||
| chr3:158827941 | AGG | A | 14 | a0001c0001t0001g0003 a0001c0001t0001g0011 a0001c0001t0001g0026 others(11): Show |
17 | HG00280.hp2 HG00408.hp2 HG00609.hp1 others(14): Show |
intron_variant | MODIFIER | c.1394+608_1394+609d others(4): Show |
MFSD1 | ENSG00000118855.21 | transcript | ENST00000415822.8 | protein_coding | 15/15 | INFO_REALIGN_3_PRIME | chr3 | 158827941 | ||||||
| chr3:158827941 | AGGGG | A | 12 | a0001c0001t0001g0003 a0001c0001t0001g0011 a0001c0001t0001g0032 others(9): Show |
13 | HG00423.hp1 HG01167.hp2 HG01168.hp2 others(10): Show |
intron_variant | MODIFIER | c.1394+606_1394+609d others(6): Show |
MFSD1 | ENSG00000118855.21 | transcript | ENST00000415822.8 | protein_coding | 15/15 | INFO_REALIGN_3_PRIME | chr3 | 158827941 | ||||||
| chr3:158827943 | G | A | 145 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0007 others(142): Show |
197 | HG00140.hp1 HG00323.hp2 HG00408.hp1 others(194): Show |
intron_variant | MODIFIER | c.1394+606G>A | MFSD1 | ENSG00000118855.21 | transcript | ENST00000415822.8 | protein_coding | 15/15 | chr3 | 158827943 | |||||||
| chr3:158827945 | G | A | 153 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0007 others(150): Show |
216 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(213): Show |
intron_variant | MODIFIER | c.1394+608G>A | MFSD1 | ENSG00000118855.21 | transcript | ENST00000415822.8 | protein_coding | 15/15 | chr3 | 158827945 | |||||||
| chr3:158827947 | A | G | 8 | a0002c0002t0001g0027 a0002c0002t0001g0057 a0002c0002t0001g0227 others(5): Show |
13 | HG00280.hp1 HG00735.hp2 HG00741.hp2 others(10): Show |
intron_variant | MODIFIER | c.1394+610A>G | MFSD1 | ENSG00000118855.21 | transcript | ENST00000415822.8 | protein_coding | 15/15 | chr3 | 158827947 | |||||||
| chr3:158827949 | A | G | 1 | a0001c0001t0001g0105 | 1 | NA18972.hp2 | intron_variant | MODIFIER | c.1394+612A>G | MFSD1 | ENSG00000118855.21 | transcript | ENST00000415822.8 | protein_coding | 15/15 | chr3 | 158827949 | |||||||
| chr3:158827955 | A | G | 1 | a0001c0001t0001g0105 | 1 | NA18972.hp2 | intron_variant | MODIFIER | c.1394+618A>G | MFSD1 | ENSG00000118855.21 | transcript | ENST00000415822.8 | protein_coding | 15/15 | chr3 | 158827955 | |||||||
| chr3:158827968 | G | C | 5 | a0002c0002t0001g0138 a0002c0002t0010g0139 a0002c0004t0001g0163 others(2): Show |
5 | HG01243.hp2 HG01433.hp2 NA18975.hp2 others(2): Show |
intron_variant | MODIFIER | c.1394+631G>C | MFSD1 | ENSG00000118855.21 | transcript | ENST00000415822.8 | protein_coding | 15/15 | chr3 | 158827968 | |||||||
| chr3:158827970 | G | C | 1 | a0001c0001t0001g0029 | 3 | HG02145.hp2 HG06807.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.1394+633G>C | MFSD1 | ENSG00000118855.21 | transcript | ENST00000415822.8 | protein_coding | 15/15 | chr3 | 158827970 | |||||||
| chr3:158827972 | G | C | 40 | a0001c0001t0001g0099 a0001c0001t0001g0230 a0002c0002t0001g0027 others(37): Show |
76 | HG00280.hp1 HG00423.hp2 HG00609.hp2 others(73): Show |
intron_variant | MODIFIER | c.1394+635G>C | MFSD1 | ENSG00000118855.21 | transcript | ENST00000415822.8 | protein_coding | 15/15 | chr3 | 158827972 | |||||||
| chr3:158827976 | G | C | 132 | a0001c0001t0001g0003 a0001c0001t0001g0010 a0001c0001t0001g0011 others(129): Show |
250 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(247): Show |
intron_variant | MODIFIER | c.1394+639G>C | MFSD1 | ENSG00000118855.21 | transcript | ENST00000415822.8 | protein_coding | 15/15 | chr3 | 158827976 | |||||||
| chr3:158827976 | G | GAC | 19 | a0001c0001t0001g0034 a0001c0001t0001g0039 a0001c0001t0001g0056 others(16): Show |
23 | HG00733.hp2 HG00738.hp1 HG01069.hp1 others(20): Show |
intron_variant | MODIFIER | c.1394+640_1394+641i others(4): Show |
MFSD1 | ENSG00000118855.21 | transcript | ENST00000415822.8 | protein_coding | 15/15 | INFO_REALIGN_3_PRIME | chr3 | 158827976 | ||||||
| chr3:158827976 | G | GACAGACA others(3): Show |
2 | a0001c0001t0001g0100 a0002c0002t0001g0202 |
2 | HG00642.hp1 NA19083.hp2 |
intron_variant | MODIFIER | c.1394+640_1394+641i others(12): Show |
MFSD1 | ENSG00000118855.21 | transcript | ENST00000415822.8 | protein_coding | 15/15 | INFO_REALIGN_3_PRIME | chr3 | 158827976 | ||||||
| chr3:158827976 | G | GACAGAGA others(3): Show |
1 | a0002c0002t0001g0216 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.1394+640_1394+641i others(12): Show |
MFSD1 | ENSG00000118855.21 | transcript | ENST00000415822.8 | protein_coding | 15/15 | INFO_REALIGN_3_PRIME | chr3 | 158827976 | ||||||
| chr3:158827976 | G | GAGAC | 19 | a0001c0001t0001g0007 a0001c0001t0001g0016 a0001c0001t0001g0059 others(16): Show |
27 | HG00140.hp1 HG00621.hp1 HG00621.hp2 others(24): Show |
intron_variant | MODIFIER | c.1394+643_1394+646d others(6): Show |
MFSD1 | ENSG00000118855.21 | transcript | ENST00000415822.8 | protein_coding | 15/15 | INFO_REALIGN_3_PRIME | chr3 | 158827976 | ||||||
| chr3:158827976 | G | GAGAGAC | 14 | a0001c0001t0001g0005 a0001c0001t0001g0012 a0001c0001t0001g0028 others(11): Show |
28 | HG00323.hp2 HG00639.hp2 HG00738.hp2 others(25): Show |
intron_variant | MODIFIER | c.1394+642_1394+643i others(8): Show |
MFSD1 | ENSG00000118855.21 | transcript | ENST00000415822.8 | protein_coding | 15/15 | INFO_REALIGN_3_PRIME | chr3 | 158827976 | ||||||
| chr3:158827976 | G | GAGAGACA others(7): Show |
1 | a0002c0002t0001g0205 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.1394+642_1394+643i others(16): Show |
MFSD1 | ENSG00000118855.21 | transcript | ENST00000415822.8 | protein_coding | 15/15 | INFO_REALIGN_3_PRIME | chr3 | 158827976 | ||||||
| chr3:158827976 | G | GAGAGAGA others(1): Show |
15 | a0001c0001t0001g0035 a0001c0001t0001g0037 a0001c0001t0001g0072 others(12): Show |
17 | HG00558.hp1 HG01109.hp2 HG01496.hp2 others(14): Show |
intron_variant | MODIFIER | c.1394+642_1394+643i others(10): Show |
MFSD1 | ENSG00000118855.21 | transcript | ENST00000415822.8 | protein_coding | 15/15 | INFO_REALIGN_3_PRIME | chr3 | 158827976 | ||||||
| chr3:158827976 | G | GAGAGAGA others(9): Show |
1 | a0001c0001t0004g0110 | 1 | NA19054.hp2 | intron_variant | MODIFIER | c.1394+642_1394+643i others(18): Show |
MFSD1 | ENSG00000118855.21 | transcript | ENST00000415822.8 | protein_coding | 15/15 | INFO_REALIGN_3_PRIME | chr3 | 158827976 | ||||||
| chr3:158827976 | G | GAGAGAGA others(3): Show |
10 | a0001c0001t0001g0068 a0001c0001t0001g0090 a0001c0001t0001g0112 others(7): Show |
10 | HG01993.hp2 HG02135.hp1 HG02145.hp1 others(7): Show |
intron_variant | MODIFIER | c.1394+642_1394+643i others(12): Show |
MFSD1 | ENSG00000118855.21 | transcript | ENST00000415822.8 | protein_coding | 15/15 | INFO_REALIGN_3_PRIME | chr3 | 158827976 | ||||||
| chr3:158827976 | G | GAGAGAGA others(5): Show |
4 | a0001c0001t0001g0018 a0001c0001t0001g0067 a0001c0001t0001g0097 others(1): Show |
6 | HG01433.hp1 HG01934.hp2 HG04228.hp1 others(3): Show |
intron_variant | MODIFIER | c.1394+642_1394+643i others(14): Show |
MFSD1 | ENSG00000118855.21 | transcript | ENST00000415822.8 | protein_coding | 15/15 | INFO_REALIGN_3_PRIME | chr3 | 158827976 | ||||||
| chr3:158827976 | G | GAGAGAGA others(13): Show |
1 | a0002c0002t0001g0218 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.1394+642_1394+643i others(22): Show |
MFSD1 | ENSG00000118855.21 | transcript | ENST00000415822.8 | protein_coding | 15/15 | INFO_REALIGN_3_PRIME | chr3 | 158827976 | ||||||
| chr3:158827976 | G | GAGAGAGA others(7): Show |
4 | a0001c0001t0001g0104 a0001c0001t0001g0109 a0001c0001t0011g0106 others(1): Show |
4 | HG01978.hp2 HG01981.hp1 HG02129.hp2 others(1): Show |
intron_variant | MODIFIER | c.1394+642_1394+643i others(16): Show |
MFSD1 | ENSG00000118855.21 | transcript | ENST00000415822.8 | protein_coding | 15/15 | INFO_REALIGN_3_PRIME | chr3 | 158827976 | ||||||
| chr3:158827976 | G | GAGAGAGA others(9): Show |
2 | a0001c0001t0001g0231 a0002c0002t0001g0208 |
2 | HG02258.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.1394+642_1394+643i others(18): Show |
MFSD1 | ENSG00000118855.21 | transcript | ENST00000415822.8 | protein_coding | 15/15 | INFO_REALIGN_3_PRIME | chr3 | 158827976 | ||||||
| chr3:158827976 | G | GAGAGAGA others(11): Show |
1 | a0001c0001t0001g0071 | 1 | NA18988.hp2 | intron_variant | MODIFIER | c.1394+642_1394+643i others(20): Show |
MFSD1 | ENSG00000118855.21 | transcript | ENST00000415822.8 | protein_coding | 15/15 | INFO_REALIGN_3_PRIME | chr3 | 158827976 | ||||||
| chr3:158827978 | G | GAGAGAGA others(3): Show |
2 | a0004c0005t0001g0199 a0004c0005t0001g0210 |
2 | HG02630.hp2 HG02818.hp2 |
intron_variant | MODIFIER | c.1394+642_1394+643i others(12): Show |
MFSD1 | ENSG00000118855.21 | transcript | ENST00000415822.8 | protein_coding | 15/15 | INFO_REALIGN_3_PRIME | chr3 | 158827978 | ||||||
| chr3:158828026 | C | T | 16 | a0001c0001t0001g0010 a0001c0001t0001g0061 a0001c0001t0001g0157 others(13): Show |
33 | HG00408.hp1 HG00558.hp2 HG01074.hp1 others(30): Show |
intron_variant | MODIFIER | c.1394+689C>T | MFSD1 | ENSG00000118855.21 | transcript | ENST00000415822.8 | protein_coding | 15/15 | chr3 | 158828026 | |||||||
| chr3:158828037 | C | A | 6 | a0002c0002t0003g0015 a0002c0002t0003g0043 a0002c0002t0003g0140 others(3): Show |
11 | HG01255.hp1 HG02257.hp2 HG02451.hp1 others(8): Show |
intron_variant | MODIFIER | c.1394+700C>A | MFSD1 | ENSG00000118855.21 | transcript | ENST00000415822.8 | protein_coding | 15/15 | chr3 | 158828037 | |||||||
| chr3:158828109 | C | T | 1 | a0001c0001t0001g0105 | 1 | NA18972.hp2 | intron_variant | MODIFIER | c.1394+772C>T | MFSD1 | ENSG00000118855.21 | transcript | ENST00000415822.8 | protein_coding | 15/15 | chr3 | 158828109 | |||||||
| chr3:158828123 | A | G | 45 | a0002c0002t0001g0027 a0002c0002t0001g0057 a0002c0002t0001g0227 others(42): Show |
90 | HG00280.hp1 HG00423.hp2 HG00609.hp2 others(87): Show |
intron_variant | MODIFIER | c.1394+786A>G | MFSD1 | ENSG00000118855.21 | transcript | ENST00000415822.8 | protein_coding | 15/15 | chr3 | 158828123 | |||||||
| chr3:158828305 | A | G | 3 | a0002c0004t0001g0163 a0002c0004t0001g0164 a0002c0004t0001g0165 |
3 | NA18975.hp2 NA19078.hp2 NA19091.hp1 |
intron_variant | MODIFIER | c.1395-674A>G | MFSD1 | ENSG00000118855.21 | transcript | ENST00000415822.8 | protein_coding | 15/15 | chr3 | 158828305 | |||||||
| chr3:158828440 | A | G | 1 | a0001c0001t0001g0103 | 1 | HG02273.hp2 | intron_variant | MODIFIER | c.1395-539A>G | MFSD1 | ENSG00000118855.21 | transcript | ENST00000415822.8 | protein_coding | 15/15 | chr3 | 158828440 | |||||||
| chr3:158828763 | ATATT | A | 32 | a0002c0002t0001g0027 a0002c0002t0001g0057 a0002c0002t0001g0227 others(29): Show |
68 | HG00280.hp1 HG00423.hp2 HG00609.hp2 others(65): Show |
intron_variant | MODIFIER | c.1395-215_1395-212d others(6): Show |
MFSD1 | ENSG00000118855.21 | transcript | ENST00000415822.8 | protein_coding | 15/15 | chr3 | 158828763 | |||||||
| chr3:158828793 | A | G | 2 | a0002c0002t0003g0043 a0002c0002t0003g0140 |
3 | HG03041.hp1 HG03579.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.1395-186A>G | MFSD1 | ENSG00000118855.21 | transcript | ENST00000415822.8 | protein_coding | 15/15 | chr3 | 158828793 | |||||||
| chr3:158828852 | GA | G | 6 | a0002c0002t0003g0015 a0002c0002t0003g0043 a0002c0002t0003g0140 others(3): Show |
11 | HG01255.hp1 HG02257.hp2 HG02451.hp1 others(8): Show |
intron_variant | MODIFIER | c.1395-119delA | MFSD1 | ENSG00000118855.21 | transcript | ENST00000415822.8 | protein_coding | 15/15 | INFO_REALIGN_3_PRIME | chr3 | 158828852 |