Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 256471 |
| ensemblid | ENSG00000164073.11 |
| hgncid | 28486 |
| symbol | MFSD8 |
| name | major facilitator superfamily domain containing 8 |
| refseq_nuc | NM_001371596.2 |
| refseq_prot | NP_001358525.1 |
| ensembl_nuc | ENST00000641686.2 |
| ensembl_prot | ENSP00000493218.2 |
| mane_status | MANE Select |
| chr | chr4 |
| start | 127917805 |
| end | 127965173 |
| strand | - |
| ver | v1.2 |
| region | chr4:127917805-127965173 |
| region5000 | chr4:127912805-127970173 |
| regionname0 | MFSD8_chr4_127917805_127965173 |
| regionname5000 | MFSD8_chr4_127912805_127970173 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 518 | 243 | 69 | 35 | 95 | 12 | 30 | 71 | MFSD8_chr4_127912805_127970173 | MFSD8 | MAGLR others(513): Show |
chr4 | 127912805 | 127970173 |
| a0002 | 0/0 | 518 | 88 | 19 | 7 | 62 | 0 | 0 | 50 | MFSD8_chr4_127912805_127970173 | MFSD8 | MAGLR others(513): Show |
chr4 | 127912805 | 127970173 |
| a0003 | 0/0 | 518 | 16 | 0 | 3 | 13 | 0 | 0 | 7 | MFSD8_chr4_127912805_127970173 | MFSD8 | MAGLR others(513): Show |
chr4 | 127912805 | 127970173 |
| a0004 | 0/0 | 518 | 3 | 2 | 1 | 0 | 0 | 0 | 0 | MFSD8_chr4_127912805_127970173 | MFSD8 | MAGLR others(513): Show |
chr4 | 127912805 | 127970173 |
| a0005 | 0/0 | 518 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | MFSD8_chr4_127912805_127970173 | MFSD8 | MAGLR others(513): Show |
chr4 | 127912805 | 127970173 |
| a0006 | 0/0 | 518 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | MFSD8_chr4_127912805_127970173 | MFSD8 | MAGLR others(513): Show |
chr4 | 127912805 | 127970173 |
| a0007 | 0/0 | 518 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | MFSD8_chr4_127912805_127970173 | MFSD8 | MAGLR others(513): Show |
chr4 | 127912805 | 127970173 |
| a0008 | 0/0 | 518 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | MFSD8_chr4_127912805_127970173 | MFSD8 | MAGLR others(513): Show |
chr4 | 127912805 | 127970173 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 1554 | 240 | 68 | 35 | 95 | 12 | 28 | MFSD8_chr4_127912805_127970173 | MFSD8 | ATGGC others(1549): Show |
chr4 | 127912805 | 127970173 | ||
| a0001c0005 | 0/0 | 1554 | 2 | 0 | 0 | 0 | 0 | 2 | MFSD8_chr4_127912805_127970173 | MFSD8 | ATGGC others(1549): Show |
chr4 | 127912805 | 127970173 | ||
| a0001c0009 | 0/0 | 1554 | 1 | 1 | 0 | 0 | 0 | 0 | MFSD8_chr4_127912805_127970173 | MFSD8 | ATGGC others(1549): Show |
chr4 | 127912805 | 127970173 | ||
| a0002c0002 | 0/0 | 1554 | 88 | 19 | 7 | 62 | 0 | 0 | MFSD8_chr4_127912805_127970173 | MFSD8 | ATGGC others(1549): Show |
chr4 | 127912805 | 127970173 | ||
| a0003c0003 | 0/0 | 1554 | 16 | 0 | 3 | 13 | 0 | 0 | MFSD8_chr4_127912805_127970173 | MFSD8 | ATGGC others(1549): Show |
chr4 | 127912805 | 127970173 | ||
| a0004c0004 | 0/0 | 1554 | 3 | 2 | 1 | 0 | 0 | 0 | MFSD8_chr4_127912805_127970173 | MFSD8 | ATGGC others(1549): Show |
chr4 | 127912805 | 127970173 | ||
| a0005c0007 | 0/0 | 1554 | 1 | 1 | 0 | 0 | 0 | 0 | MFSD8_chr4_127912805_127970173 | MFSD8 | ATGGC others(1549): Show |
chr4 | 127912805 | 127970173 | ||
| a0006c0006 | 0/0 | 1554 | 1 | 1 | 0 | 0 | 0 | 0 | MFSD8_chr4_127912805_127970173 | MFSD8 | ATGGC others(1549): Show |
chr4 | 127912805 | 127970173 | ||
| a0007c0010 | 0/0 | 1554 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD8_chr4_127912805_127970173 | MFSD8 | ATGGC others(1549): Show |
chr4 | 127912805 | 127970173 | ||
| a0008c0008 | 0/0 | 1554 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD8_chr4_127912805_127970173 | MFSD8 | ATGGC others(1549): Show |
chr4 | 127912805 | 127970173 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 1/1 | 4422 | 224 | 63 | 35 | 84 | 12 | 28 | MFSD8_chr4_127912805_127970173 | MFSD8 | GCGAG others(4417): Show |
chr4 | 127912805 | 127970173 |
| a0001c0001t0007 | 0/0 | 4422 | 4 | 0 | 0 | 4 | 0 | 0 | MFSD8_chr4_127912805_127970173 | MFSD8 | GCGAG others(4417): Show |
chr4 | 127912805 | 127970173 |
| a0001c0001t0008 | 0/0 | 4422 | 3 | 0 | 0 | 3 | 0 | 0 | MFSD8_chr4_127912805_127970173 | MFSD8 | GCGAG others(4417): Show |
chr4 | 127912805 | 127970173 |
| a0001c0001t0011 | 0/0 | 4422 | 2 | 0 | 0 | 2 | 0 | 0 | MFSD8_chr4_127912805_127970173 | MFSD8 | GCGAG others(4417): Show |
chr4 | 127912805 | 127970173 |
| a0001c0001t0015 | 0/0 | 4422 | 1 | 1 | 0 | 0 | 0 | 0 | MFSD8_chr4_127912805_127970173 | MFSD8 | GCGAG others(4417): Show |
chr4 | 127912805 | 127970173 |
| a0001c0001t0016 | 0/0 | 4422 | 1 | 1 | 0 | 0 | 0 | 0 | MFSD8_chr4_127912805_127970173 | MFSD8 | GCGAG others(4417): Show |
chr4 | 127912805 | 127970173 |
| a0001c0001t0017 | 0/0 | 4422 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD8_chr4_127912805_127970173 | MFSD8 | GCGAG others(4417): Show |
chr4 | 127912805 | 127970173 |
| a0001c0001t0018 | 0/0 | 4422 | 1 | 1 | 0 | 0 | 0 | 0 | MFSD8_chr4_127912805_127970173 | MFSD8 | GCGAG others(4417): Show |
chr4 | 127912805 | 127970173 |
| a0001c0001t0019 | 0/0 | 4422 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD8_chr4_127912805_127970173 | MFSD8 | GCGAG others(4417): Show |
chr4 | 127912805 | 127970173 |
| a0001c0001t0020 | 0/0 | 4422 | 1 | 1 | 0 | 0 | 0 | 0 | MFSD8_chr4_127912805_127970173 | MFSD8 | GCGAG others(4417): Show |
chr4 | 127912805 | 127970173 |
| a0001c0001t0022 | 0/0 | 4422 | 1 | 1 | 0 | 0 | 0 | 0 | MFSD8_chr4_127912805_127970173 | MFSD8 | GCGAG others(4417): Show |
chr4 | 127912805 | 127970173 |
| a0001c0005t0001 | 0/0 | 4422 | 2 | 0 | 0 | 0 | 0 | 2 | MFSD8_chr4_127912805_127970173 | MFSD8 | GCGAG others(4417): Show |
chr4 | 127912805 | 127970173 |
| a0001c0009t0014 | 0/0 | 4422 | 1 | 1 | 0 | 0 | 0 | 0 | MFSD8_chr4_127912805_127970173 | MFSD8 | GCGAG others(4417): Show |
chr4 | 127912805 | 127970173 |
| a0002c0002t0002 | 0/0 | 4422 | 62 | 0 | 5 | 57 | 0 | 0 | MFSD8_chr4_127912805_127970173 | MFSD8 | GCGAG others(4417): Show |
chr4 | 127912805 | 127970173 |
| a0002c0002t0003 | 0/0 | 4422 | 11 | 11 | 0 | 0 | 0 | 0 | MFSD8_chr4_127912805_127970173 | MFSD8 | GCGAG others(4417): Show |
chr4 | 127912805 | 127970173 |
| a0002c0002t0004 | 0/0 | 4416 | 5 | 0 | 2 | 3 | 0 | 0 | MFSD8_chr4_127912805_127970173 | MFSD8 | GCGAG others(4411): Show |
chr4 | 127912805 | 127970173 |
| a0002c0002t0005 | 0/0 | 4422 | 3 | 3 | 0 | 0 | 0 | 0 | MFSD8_chr4_127912805_127970173 | MFSD8 | GCGAG others(4417): Show |
chr4 | 127912805 | 127970173 |
| a0002c0002t0006 | 0/0 | 4424 | 4 | 4 | 0 | 0 | 0 | 0 | MFSD8_chr4_127912805_127970173 | MFSD8 | GCGAG others(4419): Show |
chr4 | 127912805 | 127970173 |
| a0002c0002t0012 | 0/0 | 4422 | 1 | 1 | 0 | 0 | 0 | 0 | MFSD8_chr4_127912805_127970173 | MFSD8 | GCGAG others(4417): Show |
chr4 | 127912805 | 127970173 |
| a0002c0002t0013 | 0/0 | 4422 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD8_chr4_127912805_127970173 | MFSD8 | GCGAG others(4417): Show |
chr4 | 127912805 | 127970173 |
| a0002c0002t0023 | 0/0 | 4422 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD8_chr4_127912805_127970173 | MFSD8 | GCGAG others(4417): Show |
chr4 | 127912805 | 127970173 |
| a0003c0003t0001 | 0/0 | 4422 | 13 | 0 | 1 | 12 | 0 | 0 | MFSD8_chr4_127912805_127970173 | MFSD8 | GCGAG others(4417): Show |
chr4 | 127912805 | 127970173 |
| a0003c0003t0009 | 0/0 | 4422 | 2 | 0 | 2 | 0 | 0 | 0 | MFSD8_chr4_127912805_127970173 | MFSD8 | GCGAG others(4417): Show |
chr4 | 127912805 | 127970173 |
| a0003c0003t0021 | 0/0 | 4422 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD8_chr4_127912805_127970173 | MFSD8 | GCGAG others(4417): Show |
chr4 | 127912805 | 127970173 |
| a0004c0004t0005 | 0/0 | 4422 | 1 | 1 | 0 | 0 | 0 | 0 | MFSD8_chr4_127912805_127970173 | MFSD8 | GCGAG others(4417): Show |
chr4 | 127912805 | 127970173 |
| a0004c0004t0010 | 0/0 | 4422 | 2 | 1 | 1 | 0 | 0 | 0 | MFSD8_chr4_127912805_127970173 | MFSD8 | GCGAG others(4417): Show |
chr4 | 127912805 | 127970173 |
| a0005c0007t0001 | 0/0 | 4422 | 1 | 1 | 0 | 0 | 0 | 0 | MFSD8_chr4_127912805_127970173 | MFSD8 | GCGAG others(4417): Show |
chr4 | 127912805 | 127970173 |
| a0006c0006t0001 | 0/0 | 4422 | 1 | 1 | 0 | 0 | 0 | 0 | MFSD8_chr4_127912805_127970173 | MFSD8 | GCGAG others(4417): Show |
chr4 | 127912805 | 127970173 |
| a0007c0010t0002 | 0/0 | 4422 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD8_chr4_127912805_127970173 | MFSD8 | GCGAG others(4417): Show |
chr4 | 127912805 | 127970173 |
| a0008c0008t0001 | 0/0 | 4422 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD8_chr4_127912805_127970173 | MFSD8 | GCGAG others(4417): Show |
chr4 | 127912805 | 127970173 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 0/0 | 6 | 0 | 0 | 5 | 0 | 1 | MFSD8_chr4_127912805_127970173 | MFSD8 | chr4 | 127912805 | 127970173 |
| a0001c0001t0001g0002 | 0/0 | 6 | 0 | 0 | 6 | 0 | 0 | MFSD8_chr4_127912805_127970173 | MFSD8 | chr4 | 127912805 | 127970173 |
| a0001c0001t0001g0003 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | MFSD8_chr4_127912805_127970173 | MFSD8 | chr4 | 127912805 | 127970173 |
| a0001c0001t0001g0005 | 0/0 | 3 | 0 | 0 | 1 | 0 | 2 | MFSD8_chr4_127912805_127970173 | MFSD8 | chr4 | 127912805 | 127970173 |
| a0001c0001t0001g0006 | 0/0 | 3 | 0 | 0 | 2 | 0 | 1 | MFSD8_chr4_127912805_127970173 | MFSD8 | chr4 | 127912805 | 127970173 |
| a0001c0001t0001g0012 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MFSD8_chr4_127912805_127970173 | MFSD8 | chr4 | 127912805 | 127970173 |
| a0001c0001t0001g0013 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | MFSD8_chr4_127912805_127970173 | MFSD8 | chr4 | 127912805 | 127970173 |
| a0001c0001t0001g0014 | 0/0 | 2 | 1 | 0 | 0 | 0 | 1 | MFSD8_chr4_127912805_127970173 | MFSD8 | chr4 | 127912805 | 127970173 |
| a0001c0001t0001g0015 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | MFSD8_chr4_127912805_127970173 | MFSD8 | chr4 | 127912805 | 127970173 |
| a0001c0001t0001g0017 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MFSD8_chr4_127912805_127970173 | MFSD8 | chr4 | 127912805 | 127970173 |
| a0001c0001t0001g0018 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MFSD8_chr4_127912805_127970173 | MFSD8 | chr4 | 127912805 | 127970173 |
| a0001c0001t0001g0019 | 1/0 | 2 | 0 | 1 | 0 | 0 | 0 | MFSD8_chr4_127912805_127970173 | MFSD8 | chr4 | 127912805 | 127970173 |
| a0001c0001t0001g0020 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MFSD8_chr4_127912805_127970173 | MFSD8 | chr4 | 127912805 | 127970173 |
| a0001c0001t0001g0021 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | MFSD8_chr4_127912805_127970173 | MFSD8 | chr4 | 127912805 | 127970173 |
| a0001c0001t0001g0022 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | MFSD8_chr4_127912805_127970173 | MFSD8 | chr4 | 127912805 | 127970173 |
| a0001c0001t0001g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFSD8_chr4_127912805_127970173 | MFSD8 | chr4 | 127912805 | 127970173 |
| a0001c0001t0001g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD8_chr4_127912805_127970173 | MFSD8 | chr4 | 127912805 | 127970173 |
| a0001c0001t0001g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD8_chr4_127912805_127970173 | MFSD8 | chr4 | 127912805 | 127970173 |
| a0001c0001t0001g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD8_chr4_127912805_127970173 | MFSD8 | chr4 | 127912805 | 127970173 |
| a0001c0001t0001g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD8_chr4_127912805_127970173 | MFSD8 | chr4 | 127912805 | 127970173 |
| a0001c0001t0001g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFSD8_chr4_127912805_127970173 | MFSD8 | chr4 | 127912805 | 127970173 |
| a0001c0001t0001g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFSD8_chr4_127912805_127970173 | MFSD8 | chr4 | 127912805 | 127970173 |
| a0001c0001t0001g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFSD8_chr4_127912805_127970173 | MFSD8 | chr4 | 127912805 | 127970173 |
| a0001c0001t0001g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD8_chr4_127912805_127970173 | MFSD8 | chr4 | 127912805 | 127970173 |
| a0001c0001t0001g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFSD8_chr4_127912805_127970173 | MFSD8 | chr4 | 127912805 | 127970173 |
| a0001c0001t0001g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFSD8_chr4_127912805_127970173 | MFSD8 | chr4 | 127912805 | 127970173 |
| a0001c0001t0001g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFSD8_chr4_127912805_127970173 | MFSD8 | chr4 | 127912805 | 127970173 |
| a0001c0001t0001g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFSD8_chr4_127912805_127970173 | MFSD8 | chr4 | 127912805 | 127970173 |
| a0001c0001t0001g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD8_chr4_127912805_127970173 | MFSD8 | chr4 | 127912805 | 127970173 |
| a0001c0001t0001g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFSD8_chr4_127912805_127970173 | MFSD8 | chr4 | 127912805 | 127970173 |
| a0001c0001t0001g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD8_chr4_127912805_127970173 | MFSD8 | chr4 | 127912805 | 127970173 |
| a0001c0001t0001g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFSD8_chr4_127912805_127970173 | MFSD8 | chr4 | 127912805 | 127970173 |
| a0001c0001t0001g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFSD8_chr4_127912805_127970173 | MFSD8 | chr4 | 127912805 | 127970173 |
| a0001c0001t0001g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFSD8_chr4_127912805_127970173 | MFSD8 | chr4 | 127912805 | 127970173 |
| a0001c0001t0001g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD8_chr4_127912805_127970173 | MFSD8 | chr4 | 127912805 | 127970173 |
| a0001c0001t0001g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFSD8_chr4_127912805_127970173 | MFSD8 | chr4 | 127912805 | 127970173 |
| a0001c0001t0001g0123 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MFSD8_chr4_127912805_127970173 | MFSD8 | chr4 | 127912805 | 127970173 |
| a0001c0001t0001g0124 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MFSD8_chr4_127912805_127970173 | MFSD8 | chr4 | 127912805 | 127970173 |
| a0001c0001t0001g0125 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MFSD8_chr4_127912805_127970173 | MFSD8 | chr4 | 127912805 | 127970173 |
| a0001c0001t0001g0126 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MFSD8_chr4_127912805_127970173 | MFSD8 | chr4 | 127912805 | 127970173 |
| a0001c0001t0001g0127 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MFSD8_chr4_127912805_127970173 | MFSD8 | chr4 | 127912805 | 127970173 |
| a0001c0001t0001g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD8_chr4_127912805_127970173 | MFSD8 | chr4 | 127912805 | 127970173 |
| a0001c0001t0001g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD8_chr4_127912805_127970173 | MFSD8 | chr4 | 127912805 | 127970173 |
| a0001c0001t0001g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFSD8_chr4_127912805_127970173 | MFSD8 | chr4 | 127912805 | 127970173 |
| a0001c0001t0001g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFSD8_chr4_127912805_127970173 | MFSD8 | chr4 | 127912805 | 127970173 |
| a0001c0001t0001g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD8_chr4_127912805_127970173 | MFSD8 | chr4 | 127912805 | 127970173 |
| a0001c0001t0001g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFSD8_chr4_127912805_127970173 | MFSD8 | chr4 | 127912805 | 127970173 |
| a0001c0001t0001g0135 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MFSD8_chr4_127912805_127970173 | MFSD8 | chr4 | 127912805 | 127970173 |
| a0001c0001t0001g0136 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MFSD8_chr4_127912805_127970173 | MFSD8 | chr4 | 127912805 | 127970173 |
| a0001c0001t0001g0137 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | MFSD8_chr4_127912805_127970173 | MFSD8 | chr4 | 127912805 | 127970173 |
| a0001c0001t0001g0138 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MFSD8_chr4_127912805_127970173 | MFSD8 | chr4 | 127912805 | 127970173 |
| a0001c0001t0001g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFSD8_chr4_127912805_127970173 | MFSD8 | chr4 | 127912805 | 127970173 |
| a0001c0001t0001g0142 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MFSD8_chr4_127912805_127970173 | MFSD8 | chr4 | 127912805 | 127970173 |
| a0001c0001t0001g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD8_chr4_127912805_127970173 | MFSD8 | chr4 | 127912805 | 127970173 |
| a0001c0001t0001g0144 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MFSD8_chr4_127912805_127970173 | MFSD8 | chr4 | 127912805 | 127970173 |
| a0001c0001t0001g0145 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MFSD8_chr4_127912805_127970173 | MFSD8 | chr4 | 127912805 | 127970173 |
| a0001c0001t0001g0146 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MFSD8_chr4_127912805_127970173 | MFSD8 | chr4 | 127912805 | 127970173 |
| a0001c0001t0001g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD8_chr4_127912805_127970173 | MFSD8 | chr4 | 127912805 | 127970173 |
| a0001c0001t0001g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFSD8_chr4_127912805_127970173 | MFSD8 | chr4 | 127912805 | 127970173 |
| a0001c0001t0001g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFSD8_chr4_127912805_127970173 | MFSD8 | chr4 | 127912805 | 127970173 |
| a0001c0001t0001g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFSD8_chr4_127912805_127970173 | MFSD8 | chr4 | 127912805 | 127970173 |
| a0001c0001t0001g0152 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MFSD8_chr4_127912805_127970173 | MFSD8 | chr4 | 127912805 | 127970173 |
| a0001c0001t0001g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFSD8_chr4_127912805_127970173 | MFSD8 | chr4 | 127912805 | 127970173 |
| a0001c0001t0001g0155 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MFSD8_chr4_127912805_127970173 | MFSD8 | chr4 | 127912805 | 127970173 |
| a0001c0001t0001g0156 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MFSD8_chr4_127912805_127970173 | MFSD8 | chr4 | 127912805 | 127970173 |
| a0001c0001t0001g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD8_chr4_127912805_127970173 | MFSD8 | chr4 | 127912805 | 127970173 |
| a0001c0001t0001g0160 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MFSD8_chr4_127912805_127970173 | MFSD8 | chr4 | 127912805 | 127970173 |
| a0001c0001t0001g0161 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MFSD8_chr4_127912805_127970173 | MFSD8 | chr4 | 127912805 | 127970173 |
| a0001c0001t0001g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFSD8_chr4_127912805_127970173 | MFSD8 | chr4 | 127912805 | 127970173 |
| a0001c0001t0001g0164 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MFSD8_chr4_127912805_127970173 | MFSD8 | chr4 | 127912805 | 127970173 |
| a0001c0001t0001g0166 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MFSD8_chr4_127912805_127970173 | MFSD8 | chr4 | 127912805 | 127970173 |
| a0001c0001t0001g0167 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MFSD8_chr4_127912805_127970173 | MFSD8 | chr4 | 127912805 | 127970173 |
| a0001c0001t0001g0168 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MFSD8_chr4_127912805_127970173 | MFSD8 | chr4 | 127912805 | 127970173 |
| a0001c0001t0001g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFSD8_chr4_127912805_127970173 | MFSD8 | chr4 | 127912805 | 127970173 |
| a0001c0001t0001g0170 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MFSD8_chr4_127912805_127970173 | MFSD8 | chr4 | 127912805 | 127970173 |
| a0001c0001t0001g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFSD8_chr4_127912805_127970173 | MFSD8 | chr4 | 127912805 | 127970173 |
| a0001c0001t0001g0175 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MFSD8_chr4_127912805_127970173 | MFSD8 | chr4 | 127912805 | 127970173 |
| a0001c0001t0001g0176 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MFSD8_chr4_127912805_127970173 | MFSD8 | chr4 | 127912805 | 127970173 |
| a0001c0001t0001g0179 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MFSD8_chr4_127912805_127970173 | MFSD8 | chr4 | 127912805 | 127970173 |
| a0001c0001t0001g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD8_chr4_127912805_127970173 | MFSD8 | chr4 | 127912805 | 127970173 |
| a0001c0001t0001g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD8_chr4_127912805_127970173 | MFSD8 | chr4 | 127912805 | 127970173 |
| a0001c0001t0001g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD8_chr4_127912805_127970173 | MFSD8 | chr4 | 127912805 | 127970173 |
| a0001c0001t0001g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD8_chr4_127912805_127970173 | MFSD8 | chr4 | 127912805 | 127970173 |
| a0001c0001t0001g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD8_chr4_127912805_127970173 | MFSD8 | chr4 | 127912805 | 127970173 |
| a0001c0001t0001g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD8_chr4_127912805_127970173 | MFSD8 | chr4 | 127912805 | 127970173 |
| a0001c0001t0001g0186 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MFSD8_chr4_127912805_127970173 | MFSD8 | chr4 | 127912805 | 127970173 |
| a0001c0001t0001g0187 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MFSD8_chr4_127912805_127970173 | MFSD8 | chr4 | 127912805 | 127970173 |
| a0001c0001t0001g0188 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MFSD8_chr4_127912805_127970173 | MFSD8 | chr4 | 127912805 | 127970173 |
| a0001c0001t0001g0189 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MFSD8_chr4_127912805_127970173 | MFSD8 | chr4 | 127912805 | 127970173 |
| a0001c0001t0001g0190 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MFSD8_chr4_127912805_127970173 | MFSD8 | chr4 | 127912805 | 127970173 |
| a0001c0001t0001g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD8_chr4_127912805_127970173 | MFSD8 | chr4 | 127912805 | 127970173 |
| a0001c0001t0001g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD8_chr4_127912805_127970173 | MFSD8 | chr4 | 127912805 | 127970173 |
| a0001c0001t0001g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFSD8_chr4_127912805_127970173 | MFSD8 | chr4 | 127912805 | 127970173 |
| a0001c0001t0001g0194 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MFSD8_chr4_127912805_127970173 | MFSD8 | chr4 | 127912805 | 127970173 |
| a0001c0001t0001g0198 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MFSD8_chr4_127912805_127970173 | MFSD8 | chr4 | 127912805 | 127970173 |
| a0001c0001t0001g0199 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MFSD8_chr4_127912805_127970173 | MFSD8 | chr4 | 127912805 | 127970173 |
| a0001c0001t0001g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD8_chr4_127912805_127970173 | MFSD8 | chr4 | 127912805 | 127970173 |
| a0001c0001t0001g0202 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MFSD8_chr4_127912805_127970173 | MFSD8 | chr4 | 127912805 | 127970173 |
| a0001c0001t0001g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD8_chr4_127912805_127970173 | MFSD8 | chr4 | 127912805 | 127970173 |
| a0001c0001t0001g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD8_chr4_127912805_127970173 | MFSD8 | chr4 | 127912805 | 127970173 |
| a0001c0001t0001g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD8_chr4_127912805_127970173 | MFSD8 | chr4 | 127912805 | 127970173 |
| a0001c0001t0001g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD8_chr4_127912805_127970173 | MFSD8 | chr4 | 127912805 | 127970173 |
| a0001c0001t0001g0207 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MFSD8_chr4_127912805_127970173 | MFSD8 | chr4 | 127912805 | 127970173 |
| a0001c0001t0001g0208 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MFSD8_chr4_127912805_127970173 | MFSD8 | chr4 | 127912805 | 127970173 |
| a0001c0001t0001g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFSD8_chr4_127912805_127970173 | MFSD8 | chr4 | 127912805 | 127970173 |
| a0001c0001t0001g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFSD8_chr4_127912805_127970173 | MFSD8 | chr4 | 127912805 | 127970173 |
| a0001c0001t0001g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFSD8_chr4_127912805_127970173 | MFSD8 | chr4 | 127912805 | 127970173 |
| a0001c0001t0001g0212 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MFSD8_chr4_127912805_127970173 | MFSD8 | chr4 | 127912805 | 127970173 |
| a0001c0001t0001g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD8_chr4_127912805_127970173 | MFSD8 | chr4 | 127912805 | 127970173 |
| a0001c0001t0001g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD8_chr4_127912805_127970173 | MFSD8 | chr4 | 127912805 | 127970173 |
| a0001c0001t0001g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFSD8_chr4_127912805_127970173 | MFSD8 | chr4 | 127912805 | 127970173 |
| a0001c0001t0001g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFSD8_chr4_127912805_127970173 | MFSD8 | chr4 | 127912805 | 127970173 |
| a0001c0001t0001g0220 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MFSD8_chr4_127912805_127970173 | MFSD8 | chr4 | 127912805 | 127970173 |
| a0001c0001t0001g0221 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MFSD8_chr4_127912805_127970173 | MFSD8 | chr4 | 127912805 | 127970173 |
| a0001c0001t0001g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFSD8_chr4_127912805_127970173 | MFSD8 | chr4 | 127912805 | 127970173 |
| a0001c0001t0001g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFSD8_chr4_127912805_127970173 | MFSD8 | chr4 | 127912805 | 127970173 |
| a0001c0001t0001g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFSD8_chr4_127912805_127970173 | MFSD8 | chr4 | 127912805 | 127970173 |
| a0001c0001t0001g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFSD8_chr4_127912805_127970173 | MFSD8 | chr4 | 127912805 | 127970173 |
| a0001c0001t0001g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFSD8_chr4_127912805_127970173 | MFSD8 | chr4 | 127912805 | 127970173 |
| a0001c0001t0001g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFSD8_chr4_127912805_127970173 | MFSD8 | chr4 | 127912805 | 127970173 |
| a0001c0001t0001g0228 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MFSD8_chr4_127912805_127970173 | MFSD8 | chr4 | 127912805 | 127970173 |
| a0001c0001t0001g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFSD8_chr4_127912805_127970173 | MFSD8 | chr4 | 127912805 | 127970173 |
| a0001c0001t0001g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFSD8_chr4_127912805_127970173 | MFSD8 | chr4 | 127912805 | 127970173 |
| a0001c0001t0001g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFSD8_chr4_127912805_127970173 | MFSD8 | chr4 | 127912805 | 127970173 |
| a0001c0001t0001g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFSD8_chr4_127912805_127970173 | MFSD8 | chr4 | 127912805 | 127970173 |
| a0001c0001t0001g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD8_chr4_127912805_127970173 | MFSD8 | chr4 | 127912805 | 127970173 |
| a0001c0001t0001g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFSD8_chr4_127912805_127970173 | MFSD8 | chr4 | 127912805 | 127970173 |
| a0001c0001t0001g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFSD8_chr4_127912805_127970173 | MFSD8 | chr4 | 127912805 | 127970173 |
| a0001c0001t0001g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFSD8_chr4_127912805_127970173 | MFSD8 | chr4 | 127912805 | 127970173 |
| a0001c0001t0001g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFSD8_chr4_127912805_127970173 | MFSD8 | chr4 | 127912805 | 127970173 |
| a0001c0001t0001g0239 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MFSD8_chr4_127912805_127970173 | MFSD8 | chr4 | 127912805 | 127970173 |
| a0001c0001t0001g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD8_chr4_127912805_127970173 | MFSD8 | chr4 | 127912805 | 127970173 |
| a0001c0001t0001g0241 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MFSD8_chr4_127912805_127970173 | MFSD8 | chr4 | 127912805 | 127970173 |
| a0001c0001t0001g0245 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MFSD8_chr4_127912805_127970173 | MFSD8 | chr4 | 127912805 | 127970173 |
| a0001c0001t0001g0246 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MFSD8_chr4_127912805_127970173 | MFSD8 | chr4 | 127912805 | 127970173 |
| a0001c0001t0001g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD8_chr4_127912805_127970173 | MFSD8 | chr4 | 127912805 | 127970173 |
| a0001c0001t0001g0248 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MFSD8_chr4_127912805_127970173 | MFSD8 | chr4 | 127912805 | 127970173 |
| a0001c0001t0001g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD8_chr4_127912805_127970173 | MFSD8 | chr4 | 127912805 | 127970173 |
| a0001c0001t0001g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD8_chr4_127912805_127970173 | MFSD8 | chr4 | 127912805 | 127970173 |
| a0001c0001t0001g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD8_chr4_127912805_127970173 | MFSD8 | chr4 | 127912805 | 127970173 |
| a0001c0001t0001g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD8_chr4_127912805_127970173 | MFSD8 | chr4 | 127912805 | 127970173 |
| a0001c0001t0001g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD8_chr4_127912805_127970173 | MFSD8 | chr4 | 127912805 | 127970173 |
| a0001c0001t0001g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD8_chr4_127912805_127970173 | MFSD8 | chr4 | 127912805 | 127970173 |
| a0001c0001t0001g0256 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MFSD8_chr4_127912805_127970173 | MFSD8 | chr4 | 127912805 | 127970173 |
| a0001c0001t0001g0257 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFSD8_chr4_127912805_127970173 | MFSD8 | chr4 | 127912805 | 127970173 |
| a0001c0001t0001g0258 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MFSD8_chr4_127912805_127970173 | MFSD8 | chr4 | 127912805 | 127970173 |
| a0001c0001t0001g0259 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFSD8_chr4_127912805_127970173 | MFSD8 | chr4 | 127912805 | 127970173 |
| a0001c0001t0001g0260 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFSD8_chr4_127912805_127970173 | MFSD8 | chr4 | 127912805 | 127970173 |
| a0001c0001t0001g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD8_chr4_127912805_127970173 | MFSD8 | chr4 | 127912805 | 127970173 |
| a0001c0001t0001g0262 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFSD8_chr4_127912805_127970173 | MFSD8 | chr4 | 127912805 | 127970173 |
| a0001c0001t0001g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD8_chr4_127912805_127970173 | MFSD8 | chr4 | 127912805 | 127970173 |
| a0001c0001t0001g0264 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MFSD8_chr4_127912805_127970173 | MFSD8 | chr4 | 127912805 | 127970173 |
| a0001c0001t0001g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD8_chr4_127912805_127970173 | MFSD8 | chr4 | 127912805 | 127970173 |
| a0001c0001t0001g0266 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFSD8_chr4_127912805_127970173 | MFSD8 | chr4 | 127912805 | 127970173 |
| a0001c0001t0001g0267 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFSD8_chr4_127912805_127970173 | MFSD8 | chr4 | 127912805 | 127970173 |
| a0001c0001t0001g0268 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MFSD8_chr4_127912805_127970173 | MFSD8 | chr4 | 127912805 | 127970173 |
| a0001c0001t0001g0269 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MFSD8_chr4_127912805_127970173 | MFSD8 | chr4 | 127912805 | 127970173 |
| a0001c0001t0001g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD8_chr4_127912805_127970173 | MFSD8 | chr4 | 127912805 | 127970173 |
| a0001c0001t0001g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD8_chr4_127912805_127970173 | MFSD8 | chr4 | 127912805 | 127970173 |
| a0001c0001t0001g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD8_chr4_127912805_127970173 | MFSD8 | chr4 | 127912805 | 127970173 |
| a0001c0001t0001g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD8_chr4_127912805_127970173 | MFSD8 | chr4 | 127912805 | 127970173 |
| a0001c0001t0001g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD8_chr4_127912805_127970173 | MFSD8 | chr4 | 127912805 | 127970173 |
| a0001c0001t0001g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD8_chr4_127912805_127970173 | MFSD8 | chr4 | 127912805 | 127970173 |
| a0001c0001t0001g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD8_chr4_127912805_127970173 | MFSD8 | chr4 | 127912805 | 127970173 |
| a0001c0001t0001g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD8_chr4_127912805_127970173 | MFSD8 | chr4 | 127912805 | 127970173 |
| a0001c0001t0001g0278 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MFSD8_chr4_127912805_127970173 | MFSD8 | chr4 | 127912805 | 127970173 |
| a0001c0001t0001g0279 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MFSD8_chr4_127912805_127970173 | MFSD8 | chr4 | 127912805 | 127970173 |
| a0001c0001t0001g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD8_chr4_127912805_127970173 | MFSD8 | chr4 | 127912805 | 127970173 |
| a0001c0001t0001g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD8_chr4_127912805_127970173 | MFSD8 | chr4 | 127912805 | 127970173 |
| a0001c0001t0001g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD8_chr4_127912805_127970173 | MFSD8 | chr4 | 127912805 | 127970173 |
| a0001c0001t0001g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD8_chr4_127912805_127970173 | MFSD8 | chr4 | 127912805 | 127970173 |
| a0001c0001t0001g0284 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFSD8_chr4_127912805_127970173 | MFSD8 | chr4 | 127912805 | 127970173 |
| a0001c0001t0001g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD8_chr4_127912805_127970173 | MFSD8 | chr4 | 127912805 | 127970173 |
| a0001c0001t0001g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD8_chr4_127912805_127970173 | MFSD8 | chr4 | 127912805 | 127970173 |
| a0001c0001t0001g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD8_chr4_127912805_127970173 | MFSD8 | chr4 | 127912805 | 127970173 |
| a0001c0001t0001g0288 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MFSD8_chr4_127912805_127970173 | MFSD8 | chr4 | 127912805 | 127970173 |
| a0001c0001t0001g0289 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFSD8_chr4_127912805_127970173 | MFSD8 | chr4 | 127912805 | 127970173 |
| a0001c0001t0001g0290 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MFSD8_chr4_127912805_127970173 | MFSD8 | chr4 | 127912805 | 127970173 |
| a0001c0001t0001g0291 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MFSD8_chr4_127912805_127970173 | MFSD8 | chr4 | 127912805 | 127970173 |
| a0001c0001t0001g0292 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MFSD8_chr4_127912805_127970173 | MFSD8 | chr4 | 127912805 | 127970173 |
| a0001c0001t0001g0293 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MFSD8_chr4_127912805_127970173 | MFSD8 | chr4 | 127912805 | 127970173 |
| a0001c0001t0001g0294 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MFSD8_chr4_127912805_127970173 | MFSD8 | chr4 | 127912805 | 127970173 |
| a0001c0001t0001g0295 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MFSD8_chr4_127912805_127970173 | MFSD8 | chr4 | 127912805 | 127970173 |
| a0001c0001t0001g0296 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MFSD8_chr4_127912805_127970173 | MFSD8 | chr4 | 127912805 | 127970173 |
| a0001c0001t0001g0297 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MFSD8_chr4_127912805_127970173 | MFSD8 | chr4 | 127912805 | 127970173 |
| a0001c0001t0001g0298 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFSD8_chr4_127912805_127970173 | MFSD8 | chr4 | 127912805 | 127970173 |
| a0001c0001t0001g0299 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD8_chr4_127912805_127970173 | MFSD8 | chr4 | 127912805 | 127970173 |
| a0001c0001t0001g0300 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MFSD8_chr4_127912805_127970173 | MFSD8 | chr4 | 127912805 | 127970173 |
| a0001c0001t0001g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD8_chr4_127912805_127970173 | MFSD8 | chr4 | 127912805 | 127970173 |
| a0001c0001t0001g0302 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD8_chr4_127912805_127970173 | MFSD8 | chr4 | 127912805 | 127970173 |
| a0001c0001t0001g0304 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MFSD8_chr4_127912805_127970173 | MFSD8 | chr4 | 127912805 | 127970173 |
| a0001c0001t0001g0305 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFSD8_chr4_127912805_127970173 | MFSD8 | chr4 | 127912805 | 127970173 |
| a0001c0001t0001g0307 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFSD8_chr4_127912805_127970173 | MFSD8 | chr4 | 127912805 | 127970173 |
| a0001c0001t0001g0308 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFSD8_chr4_127912805_127970173 | MFSD8 | chr4 | 127912805 | 127970173 |
| a0001c0001t0001g0311 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD8_chr4_127912805_127970173 | MFSD8 | chr4 | 127912805 | 127970173 |
| a0001c0001t0001g0315 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFSD8_chr4_127912805_127970173 | MFSD8 | chr4 | 127912805 | 127970173 |
| a0001c0001t0007g0007 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MFSD8_chr4_127912805_127970173 | MFSD8 | chr4 | 127912805 | 127970173 |
| a0001c0001t0007g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD8_chr4_127912805_127970173 | MFSD8 | chr4 | 127912805 | 127970173 |
| a0001c0001t0007g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD8_chr4_127912805_127970173 | MFSD8 | chr4 | 127912805 | 127970173 |
| a0001c0001t0008g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD8_chr4_127912805_127970173 | MFSD8 | chr4 | 127912805 | 127970173 |
| a0001c0001t0008g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD8_chr4_127912805_127970173 | MFSD8 | chr4 | 127912805 | 127970173 |
| a0001c0001t0008g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD8_chr4_127912805_127970173 | MFSD8 | chr4 | 127912805 | 127970173 |
| a0001c0001t0011g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD8_chr4_127912805_127970173 | MFSD8 | chr4 | 127912805 | 127970173 |
| a0001c0001t0011g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD8_chr4_127912805_127970173 | MFSD8 | chr4 | 127912805 | 127970173 |
| a0001c0001t0015g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFSD8_chr4_127912805_127970173 | MFSD8 | chr4 | 127912805 | 127970173 |
| a0001c0001t0016g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFSD8_chr4_127912805_127970173 | MFSD8 | chr4 | 127912805 | 127970173 |
| a0001c0001t0017g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD8_chr4_127912805_127970173 | MFSD8 | chr4 | 127912805 | 127970173 |
| a0001c0001t0018g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFSD8_chr4_127912805_127970173 | MFSD8 | chr4 | 127912805 | 127970173 |
| a0001c0001t0019g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD8_chr4_127912805_127970173 | MFSD8 | chr4 | 127912805 | 127970173 |
| a0001c0001t0020g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFSD8_chr4_127912805_127970173 | MFSD8 | chr4 | 127912805 | 127970173 |
| a0001c0001t0022g0309 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFSD8_chr4_127912805_127970173 | MFSD8 | chr4 | 127912805 | 127970173 |
| a0001c0005t0001g0103 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MFSD8_chr4_127912805_127970173 | MFSD8 | chr4 | 127912805 | 127970173 |
| a0001c0005t0001g0104 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MFSD8_chr4_127912805_127970173 | MFSD8 | chr4 | 127912805 | 127970173 |
| a0001c0009t0014g0310 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFSD8_chr4_127912805_127970173 | MFSD8 | chr4 | 127912805 | 127970173 |
| a0002c0002t0002g0004 | 0/0 | 4 | 0 | 2 | 2 | 0 | 0 | MFSD8_chr4_127912805_127970173 | MFSD8 | chr4 | 127912805 | 127970173 |
| a0002c0002t0002g0008 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MFSD8_chr4_127912805_127970173 | MFSD8 | chr4 | 127912805 | 127970173 |
| a0002c0002t0002g0009 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MFSD8_chr4_127912805_127970173 | MFSD8 | chr4 | 127912805 | 127970173 |
| a0002c0002t0002g0010 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MFSD8_chr4_127912805_127970173 | MFSD8 | chr4 | 127912805 | 127970173 |
| a0002c0002t0002g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD8_chr4_127912805_127970173 | MFSD8 | chr4 | 127912805 | 127970173 |
| a0002c0002t0002g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD8_chr4_127912805_127970173 | MFSD8 | chr4 | 127912805 | 127970173 |
| a0002c0002t0002g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD8_chr4_127912805_127970173 | MFSD8 | chr4 | 127912805 | 127970173 |
| a0002c0002t0002g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD8_chr4_127912805_127970173 | MFSD8 | chr4 | 127912805 | 127970173 |
| a0002c0002t0002g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD8_chr4_127912805_127970173 | MFSD8 | chr4 | 127912805 | 127970173 |
| a0002c0002t0002g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD8_chr4_127912805_127970173 | MFSD8 | chr4 | 127912805 | 127970173 |
| a0002c0002t0002g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD8_chr4_127912805_127970173 | MFSD8 | chr4 | 127912805 | 127970173 |
| a0002c0002t0002g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD8_chr4_127912805_127970173 | MFSD8 | chr4 | 127912805 | 127970173 |
| a0002c0002t0002g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD8_chr4_127912805_127970173 | MFSD8 | chr4 | 127912805 | 127970173 |
| a0002c0002t0002g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD8_chr4_127912805_127970173 | MFSD8 | chr4 | 127912805 | 127970173 |
| a0002c0002t0002g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD8_chr4_127912805_127970173 | MFSD8 | chr4 | 127912805 | 127970173 |
| a0002c0002t0002g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD8_chr4_127912805_127970173 | MFSD8 | chr4 | 127912805 | 127970173 |
| a0002c0002t0002g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD8_chr4_127912805_127970173 | MFSD8 | chr4 | 127912805 | 127970173 |
| a0002c0002t0002g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD8_chr4_127912805_127970173 | MFSD8 | chr4 | 127912805 | 127970173 |
| a0002c0002t0002g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD8_chr4_127912805_127970173 | MFSD8 | chr4 | 127912805 | 127970173 |
| a0002c0002t0002g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD8_chr4_127912805_127970173 | MFSD8 | chr4 | 127912805 | 127970173 |
| a0002c0002t0002g0050 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MFSD8_chr4_127912805_127970173 | MFSD8 | chr4 | 127912805 | 127970173 |
| a0002c0002t0002g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD8_chr4_127912805_127970173 | MFSD8 | chr4 | 127912805 | 127970173 |
| a0002c0002t0002g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD8_chr4_127912805_127970173 | MFSD8 | chr4 | 127912805 | 127970173 |
| a0002c0002t0002g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD8_chr4_127912805_127970173 | MFSD8 | chr4 | 127912805 | 127970173 |
| a0002c0002t0002g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD8_chr4_127912805_127970173 | MFSD8 | chr4 | 127912805 | 127970173 |
| a0002c0002t0002g0056 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MFSD8_chr4_127912805_127970173 | MFSD8 | chr4 | 127912805 | 127970173 |
| a0002c0002t0002g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD8_chr4_127912805_127970173 | MFSD8 | chr4 | 127912805 | 127970173 |
| a0002c0002t0002g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD8_chr4_127912805_127970173 | MFSD8 | chr4 | 127912805 | 127970173 |
| a0002c0002t0002g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD8_chr4_127912805_127970173 | MFSD8 | chr4 | 127912805 | 127970173 |
| a0002c0002t0002g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD8_chr4_127912805_127970173 | MFSD8 | chr4 | 127912805 | 127970173 |
| a0002c0002t0002g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD8_chr4_127912805_127970173 | MFSD8 | chr4 | 127912805 | 127970173 |
| a0002c0002t0002g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD8_chr4_127912805_127970173 | MFSD8 | chr4 | 127912805 | 127970173 |
| a0002c0002t0002g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD8_chr4_127912805_127970173 | MFSD8 | chr4 | 127912805 | 127970173 |
| a0002c0002t0002g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD8_chr4_127912805_127970173 | MFSD8 | chr4 | 127912805 | 127970173 |
| a0002c0002t0002g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD8_chr4_127912805_127970173 | MFSD8 | chr4 | 127912805 | 127970173 |
| a0002c0002t0002g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD8_chr4_127912805_127970173 | MFSD8 | chr4 | 127912805 | 127970173 |
| a0002c0002t0002g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD8_chr4_127912805_127970173 | MFSD8 | chr4 | 127912805 | 127970173 |
| a0002c0002t0002g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD8_chr4_127912805_127970173 | MFSD8 | chr4 | 127912805 | 127970173 |
| a0002c0002t0002g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD8_chr4_127912805_127970173 | MFSD8 | chr4 | 127912805 | 127970173 |
| a0002c0002t0002g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD8_chr4_127912805_127970173 | MFSD8 | chr4 | 127912805 | 127970173 |
| a0002c0002t0002g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD8_chr4_127912805_127970173 | MFSD8 | chr4 | 127912805 | 127970173 |
| a0002c0002t0002g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD8_chr4_127912805_127970173 | MFSD8 | chr4 | 127912805 | 127970173 |
| a0002c0002t0002g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD8_chr4_127912805_127970173 | MFSD8 | chr4 | 127912805 | 127970173 |
| a0002c0002t0002g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD8_chr4_127912805_127970173 | MFSD8 | chr4 | 127912805 | 127970173 |
| a0002c0002t0002g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD8_chr4_127912805_127970173 | MFSD8 | chr4 | 127912805 | 127970173 |
| a0002c0002t0002g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD8_chr4_127912805_127970173 | MFSD8 | chr4 | 127912805 | 127970173 |
| a0002c0002t0002g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD8_chr4_127912805_127970173 | MFSD8 | chr4 | 127912805 | 127970173 |
| a0002c0002t0002g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD8_chr4_127912805_127970173 | MFSD8 | chr4 | 127912805 | 127970173 |
| a0002c0002t0002g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD8_chr4_127912805_127970173 | MFSD8 | chr4 | 127912805 | 127970173 |
| a0002c0002t0002g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD8_chr4_127912805_127970173 | MFSD8 | chr4 | 127912805 | 127970173 |
| a0002c0002t0002g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD8_chr4_127912805_127970173 | MFSD8 | chr4 | 127912805 | 127970173 |
| a0002c0002t0002g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MFSD8_chr4_127912805_127970173 | MFSD8 | chr4 | 127912805 | 127970173 |
| a0002c0002t0002g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD8_chr4_127912805_127970173 | MFSD8 | chr4 | 127912805 | 127970173 |
| a0002c0002t0002g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD8_chr4_127912805_127970173 | MFSD8 | chr4 | 127912805 | 127970173 |
| a0002c0002t0002g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD8_chr4_127912805_127970173 | MFSD8 | chr4 | 127912805 | 127970173 |
| a0002c0002t0002g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD8_chr4_127912805_127970173 | MFSD8 | chr4 | 127912805 | 127970173 |
| a0002c0002t0003g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFSD8_chr4_127912805_127970173 | MFSD8 | chr4 | 127912805 | 127970173 |
| a0002c0002t0003g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFSD8_chr4_127912805_127970173 | MFSD8 | chr4 | 127912805 | 127970173 |
| a0002c0002t0003g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFSD8_chr4_127912805_127970173 | MFSD8 | chr4 | 127912805 | 127970173 |
| a0002c0002t0003g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFSD8_chr4_127912805_127970173 | MFSD8 | chr4 | 127912805 | 127970173 |
| a0002c0002t0003g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFSD8_chr4_127912805_127970173 | MFSD8 | chr4 | 127912805 | 127970173 |
| a0002c0002t0003g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFSD8_chr4_127912805_127970173 | MFSD8 | chr4 | 127912805 | 127970173 |
| a0002c0002t0003g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFSD8_chr4_127912805_127970173 | MFSD8 | chr4 | 127912805 | 127970173 |
| a0002c0002t0003g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFSD8_chr4_127912805_127970173 | MFSD8 | chr4 | 127912805 | 127970173 |
| a0002c0002t0003g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFSD8_chr4_127912805_127970173 | MFSD8 | chr4 | 127912805 | 127970173 |
| a0002c0002t0003g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFSD8_chr4_127912805_127970173 | MFSD8 | chr4 | 127912805 | 127970173 |
| a0002c0002t0003g0316 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFSD8_chr4_127912805_127970173 | MFSD8 | chr4 | 127912805 | 127970173 |
| a0002c0002t0004g0034 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MFSD8_chr4_127912805_127970173 | MFSD8 | chr4 | 127912805 | 127970173 |
| a0002c0002t0004g0035 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MFSD8_chr4_127912805_127970173 | MFSD8 | chr4 | 127912805 | 127970173 |
| a0002c0002t0004g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD8_chr4_127912805_127970173 | MFSD8 | chr4 | 127912805 | 127970173 |
| a0002c0002t0004g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD8_chr4_127912805_127970173 | MFSD8 | chr4 | 127912805 | 127970173 |
| a0002c0002t0004g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD8_chr4_127912805_127970173 | MFSD8 | chr4 | 127912805 | 127970173 |
| a0002c0002t0005g0312 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFSD8_chr4_127912805_127970173 | MFSD8 | chr4 | 127912805 | 127970173 |
| a0002c0002t0005g0313 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFSD8_chr4_127912805_127970173 | MFSD8 | chr4 | 127912805 | 127970173 |
| a0002c0002t0005g0314 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFSD8_chr4_127912805_127970173 | MFSD8 | chr4 | 127912805 | 127970173 |
| a0002c0002t0006g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFSD8_chr4_127912805_127970173 | MFSD8 | chr4 | 127912805 | 127970173 |
| a0002c0002t0006g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFSD8_chr4_127912805_127970173 | MFSD8 | chr4 | 127912805 | 127970173 |
| a0002c0002t0006g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFSD8_chr4_127912805_127970173 | MFSD8 | chr4 | 127912805 | 127970173 |
| a0002c0002t0006g0306 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFSD8_chr4_127912805_127970173 | MFSD8 | chr4 | 127912805 | 127970173 |
| a0002c0002t0012g0317 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFSD8_chr4_127912805_127970173 | MFSD8 | chr4 | 127912805 | 127970173 |
| a0002c0002t0013g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD8_chr4_127912805_127970173 | MFSD8 | chr4 | 127912805 | 127970173 |
| a0002c0002t0023g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD8_chr4_127912805_127970173 | MFSD8 | chr4 | 127912805 | 127970173 |
| a0003c0003t0001g0016 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MFSD8_chr4_127912805_127970173 | MFSD8 | chr4 | 127912805 | 127970173 |
| a0003c0003t0001g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD8_chr4_127912805_127970173 | MFSD8 | chr4 | 127912805 | 127970173 |
| a0003c0003t0001g0139 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MFSD8_chr4_127912805_127970173 | MFSD8 | chr4 | 127912805 | 127970173 |
| a0003c0003t0001g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD8_chr4_127912805_127970173 | MFSD8 | chr4 | 127912805 | 127970173 |
| a0003c0003t0001g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD8_chr4_127912805_127970173 | MFSD8 | chr4 | 127912805 | 127970173 |
| a0003c0003t0001g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD8_chr4_127912805_127970173 | MFSD8 | chr4 | 127912805 | 127970173 |
| a0003c0003t0001g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD8_chr4_127912805_127970173 | MFSD8 | chr4 | 127912805 | 127970173 |
| a0003c0003t0001g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD8_chr4_127912805_127970173 | MFSD8 | chr4 | 127912805 | 127970173 |
| a0003c0003t0001g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD8_chr4_127912805_127970173 | MFSD8 | chr4 | 127912805 | 127970173 |
| a0003c0003t0001g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD8_chr4_127912805_127970173 | MFSD8 | chr4 | 127912805 | 127970173 |
| a0003c0003t0001g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD8_chr4_127912805_127970173 | MFSD8 | chr4 | 127912805 | 127970173 |
| a0003c0003t0001g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD8_chr4_127912805_127970173 | MFSD8 | chr4 | 127912805 | 127970173 |
| a0003c0003t0009g0140 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MFSD8_chr4_127912805_127970173 | MFSD8 | chr4 | 127912805 | 127970173 |
| a0003c0003t0009g0172 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MFSD8_chr4_127912805_127970173 | MFSD8 | chr4 | 127912805 | 127970173 |
| a0003c0003t0021g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD8_chr4_127912805_127970173 | MFSD8 | chr4 | 127912805 | 127970173 |
| a0004c0004t0005g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFSD8_chr4_127912805_127970173 | MFSD8 | chr4 | 127912805 | 127970173 |
| a0004c0004t0010g0011 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | MFSD8_chr4_127912805_127970173 | MFSD8 | chr4 | 127912805 | 127970173 |
| a0005c0007t0001g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFSD8_chr4_127912805_127970173 | MFSD8 | chr4 | 127912805 | 127970173 |
| a0006c0006t0001g0303 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFSD8_chr4_127912805_127970173 | MFSD8 | chr4 | 127912805 | 127970173 |
| a0007c0010t0002g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD8_chr4_127912805_127970173 | MFSD8 | chr4 | 127912805 | 127970173 |
| a0008c0008t0001g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD8_chr4_127912805_127970173 | MFSD8 | chr4 | 127912805 | 127970173 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0001 | g0166 | EUR | GBR | MFSD8_chr4_127912805_127970173 | MFSD8 | chr4 | 127912805 | 127970173 |
| HG00099 | hp2 | a0001 | c0001 | t0001 | g0264 | EUR | GBR | MFSD8_chr4_127912805_127970173 | MFSD8 | chr4 | 127912805 | 127970173 |
| HG00140 | hp1 | a0001 | c0001 | t0001 | g0135 | EUR | GBR | MFSD8_chr4_127912805_127970173 | MFSD8 | chr4 | 127912805 | 127970173 |
| HG00140 | hp2 | a0001 | c0001 | t0001 | g0136 | EUR | GBR | MFSD8_chr4_127912805_127970173 | MFSD8 | chr4 | 127912805 | 127970173 |
| HG00408 | hp1 | a0003 | c0003 | t0001 | g0200 | EAS | CHS | MFSD8_chr4_127912805_127970173 | MFSD8 | chr4 | 127912805 | 127970173 |
| HG00408 | hp2 | a0001 | c0001 | t0001 | g0280 | EAS | CHS | MFSD8_chr4_127912805_127970173 | MFSD8 | chr4 | 127912805 | 127970173 |
| HG00423 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | CHS | MFSD8_chr4_127912805_127970173 | MFSD8 | chr4 | 127912805 | 127970173 |
| HG00423 | hp2 | a0002 | c0002 | t0002 | g0051 | EAS | CHS | MFSD8_chr4_127912805_127970173 | MFSD8 | chr4 | 127912805 | 127970173 |
| HG00438 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | CHS | MFSD8_chr4_127912805_127970173 | MFSD8 | chr4 | 127912805 | 127970173 |
| HG00438 | hp2 | a0002 | c0002 | t0002 | g0008 | EAS | CHS | MFSD8_chr4_127912805_127970173 | MFSD8 | chr4 | 127912805 | 127970173 |
| HG00544 | hp1 | a0002 | c0002 | t0002 | g0010 | EAS | CHS | MFSD8_chr4_127912805_127970173 | MFSD8 | chr4 | 127912805 | 127970173 |
| HG00544 | hp2 | a0001 | c0001 | t0001 | g0201 | EAS | CHS | MFSD8_chr4_127912805_127970173 | MFSD8 | chr4 | 127912805 | 127970173 |
| HG00558 | hp1 | a0003 | c0003 | t0001 | g0016 | EAS | CHS | MFSD8_chr4_127912805_127970173 | MFSD8 | chr4 | 127912805 | 127970173 |
| HG00558 | hp2 | a0002 | c0002 | t0004 | g0053 | EAS | CHS | MFSD8_chr4_127912805_127970173 | MFSD8 | chr4 | 127912805 | 127970173 |
| HG00597 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | CHS | MFSD8_chr4_127912805_127970173 | MFSD8 | chr4 | 127912805 | 127970173 |
| HG00597 | hp2 | a0002 | c0002 | t0002 | g0047 | EAS | CHS | MFSD8_chr4_127912805_127970173 | MFSD8 | chr4 | 127912805 | 127970173 |
| HG00609 | hp1 | a0003 | c0003 | t0001 | g0195 | EAS | CHS | MFSD8_chr4_127912805_127970173 | MFSD8 | chr4 | 127912805 | 127970173 |
| HG00609 | hp2 | a0002 | c0002 | t0002 | g0055 | EAS | CHS | MFSD8_chr4_127912805_127970173 | MFSD8 | chr4 | 127912805 | 127970173 |
| HG00621 | hp1 | a0001 | c0001 | t0001 | g0254 | EAS | CHS | MFSD8_chr4_127912805_127970173 | MFSD8 | chr4 | 127912805 | 127970173 |
| HG00621 | hp2 | a0002 | c0002 | t0002 | g0077 | EAS | CHS | MFSD8_chr4_127912805_127970173 | MFSD8 | chr4 | 127912805 | 127970173 |
| HG00639 | hp1 | a0001 | c0001 | t0001 | g0179 | AMR | PUR | MFSD8_chr4_127912805_127970173 | MFSD8 | chr4 | 127912805 | 127970173 |
| HG00639 | hp2 | a0001 | c0001 | t0001 | g0245 | AMR | PUR | MFSD8_chr4_127912805_127970173 | MFSD8 | chr4 | 127912805 | 127970173 |
| HG00673 | hp1 | a0003 | c0003 | t0001 | g0134 | EAS | CHS | MFSD8_chr4_127912805_127970173 | MFSD8 | chr4 | 127912805 | 127970173 |
| HG00673 | hp2 | a0001 | c0001 | t0001 | g0025 | EAS | CHS | MFSD8_chr4_127912805_127970173 | MFSD8 | chr4 | 127912805 | 127970173 |
| HG00735 | hp1 | a0001 | c0001 | t0001 | g0228 | AMR | PUR | MFSD8_chr4_127912805_127970173 | MFSD8 | chr4 | 127912805 | 127970173 |
| HG00735 | hp2 | a0001 | c0001 | t0001 | g0291 | AMR | PUR | MFSD8_chr4_127912805_127970173 | MFSD8 | chr4 | 127912805 | 127970173 |
| HG00738 | hp1 | a0002 | c0002 | t0004 | g0034 | AMR | PUR | MFSD8_chr4_127912805_127970173 | MFSD8 | chr4 | 127912805 | 127970173 |
| HG00738 | hp2 | a0001 | c0001 | t0001 | g0138 | AMR | PUR | MFSD8_chr4_127912805_127970173 | MFSD8 | chr4 | 127912805 | 127970173 |
| HG00741 | hp1 | a0001 | c0001 | t0001 | g0304 | AMR | PUR | MFSD8_chr4_127912805_127970173 | MFSD8 | chr4 | 127912805 | 127970173 |
| HG00741 | hp2 | a0001 | c0001 | t0001 | g0198 | AMR | PUR | MFSD8_chr4_127912805_127970173 | MFSD8 | chr4 | 127912805 | 127970173 |
| HG01074 | hp1 | a0001 | c0001 | t0001 | g0296 | AMR | PUR | MFSD8_chr4_127912805_127970173 | MFSD8 | chr4 | 127912805 | 127970173 |
| HG01074 | hp2 | a0001 | c0001 | t0001 | g0168 | AMR | PUR | MFSD8_chr4_127912805_127970173 | MFSD8 | chr4 | 127912805 | 127970173 |
| HG01081 | hp1 | a0001 | c0001 | t0001 | g0152 | AMR | PUR | MFSD8_chr4_127912805_127970173 | MFSD8 | chr4 | 127912805 | 127970173 |
| HG01081 | hp2 | a0002 | c0002 | t0002 | g0004 | AMR | PUR | MFSD8_chr4_127912805_127970173 | MFSD8 | chr4 | 127912805 | 127970173 |
| HG01106 | hp1 | a0001 | c0001 | t0001 | g0189 | AMR | PUR | MFSD8_chr4_127912805_127970173 | MFSD8 | chr4 | 127912805 | 127970173 |
| HG01106 | hp2 | a0001 | c0001 | t0001 | g0268 | AMR | PUR | MFSD8_chr4_127912805_127970173 | MFSD8 | chr4 | 127912805 | 127970173 |
| HG01168 | hp1 | a0001 | c0001 | t0001 | g0126 | AMR | PUR | MFSD8_chr4_127912805_127970173 | MFSD8 | chr4 | 127912805 | 127970173 |
| HG01168 | hp2 | a0001 | c0001 | t0001 | g0022 | AMR | PUR | MFSD8_chr4_127912805_127970173 | MFSD8 | chr4 | 127912805 | 127970173 |
| HG01175 | hp1 | a0001 | c0001 | t0001 | g0295 | AMR | PUR | MFSD8_chr4_127912805_127970173 | MFSD8 | chr4 | 127912805 | 127970173 |
| HG01175 | hp2 | a0001 | c0001 | t0001 | g0269 | AMR | PUR | MFSD8_chr4_127912805_127970173 | MFSD8 | chr4 | 127912805 | 127970173 |
| HG01243 | hp1 | a0001 | c0001 | t0001 | g0167 | AMR | PUR | MFSD8_chr4_127912805_127970173 | MFSD8 | chr4 | 127912805 | 127970173 |
| HG01243 | hp2 | a0001 | c0001 | t0001 | g0019 | AMR | PUR | MFSD8_chr4_127912805_127970173 | MFSD8 | chr4 | 127912805 | 127970173 |
| HG01256 | hp1 | a0001 | c0001 | t0001 | g0241 | AMR | CLM | MFSD8_chr4_127912805_127970173 | MFSD8 | chr4 | 127912805 | 127970173 |
| HG01256 | hp2 | a0001 | c0001 | t0001 | g0145 | AMR | CLM | MFSD8_chr4_127912805_127970173 | MFSD8 | chr4 | 127912805 | 127970173 |
| HG01257 | hp1 | a0001 | c0001 | t0001 | g0144 | AMR | CLM | MFSD8_chr4_127912805_127970173 | MFSD8 | chr4 | 127912805 | 127970173 |
| HG01257 | hp2 | a0001 | c0001 | t0001 | g0207 | AMR | CLM | MFSD8_chr4_127912805_127970173 | MFSD8 | chr4 | 127912805 | 127970173 |
| HG01258 | hp1 | a0001 | c0001 | t0001 | g0279 | AMR | CLM | MFSD8_chr4_127912805_127970173 | MFSD8 | chr4 | 127912805 | 127970173 |
| HG01258 | hp2 | a0001 | c0001 | t0001 | g0208 | AMR | CLM | MFSD8_chr4_127912805_127970173 | MFSD8 | chr4 | 127912805 | 127970173 |
| HG01346 | hp1 | a0001 | c0001 | t0001 | g0290 | AMR | CLM | MFSD8_chr4_127912805_127970173 | MFSD8 | chr4 | 127912805 | 127970173 |
| HG01346 | hp2 | a0001 | c0001 | t0001 | g0146 | AMR | CLM | MFSD8_chr4_127912805_127970173 | MFSD8 | chr4 | 127912805 | 127970173 |
| HG01358 | hp1 | a0001 | c0001 | t0001 | g0199 | AMR | CLM | MFSD8_chr4_127912805_127970173 | MFSD8 | chr4 | 127912805 | 127970173 |
| HG01358 | hp2 | a0002 | c0002 | t0004 | g0035 | AMR | CLM | MFSD8_chr4_127912805_127970173 | MFSD8 | chr4 | 127912805 | 127970173 |
| HG01433 | hp1 | a0001 | c0001 | t0001 | g0123 | AMR | CLM | MFSD8_chr4_127912805_127970173 | MFSD8 | chr4 | 127912805 | 127970173 |
| HG01433 | hp2 | a0001 | c0001 | t0001 | g0246 | AMR | CLM | MFSD8_chr4_127912805_127970173 | MFSD8 | chr4 | 127912805 | 127970173 |
| HG01496 | hp1 | a0004 | c0004 | t0010 | g0011 | AMR | CLM | MFSD8_chr4_127912805_127970173 | MFSD8 | chr4 | 127912805 | 127970173 |
| HG01496 | hp2 | a0001 | c0001 | t0001 | g0176 | AMR | CLM | MFSD8_chr4_127912805_127970173 | MFSD8 | chr4 | 127912805 | 127970173 |
| HG01515 | hp1 | a0001 | c0001 | t0001 | g0292 | EUR | IBS | MFSD8_chr4_127912805_127970173 | MFSD8 | chr4 | 127912805 | 127970173 |
| HG01515 | hp2 | a0001 | c0001 | t0001 | g0015 | EUR | IBS | MFSD8_chr4_127912805_127970173 | MFSD8 | chr4 | 127912805 | 127970173 |
| HG01516 | hp1 | a0001 | c0001 | t0001 | g0155 | EUR | IBS | MFSD8_chr4_127912805_127970173 | MFSD8 | chr4 | 127912805 | 127970173 |
| HG01516 | hp2 | a0001 | c0001 | t0001 | g0021 | EUR | IBS | MFSD8_chr4_127912805_127970173 | MFSD8 | chr4 | 127912805 | 127970173 |
| HG01517 | hp1 | a0001 | c0001 | t0001 | g0021 | EUR | IBS | MFSD8_chr4_127912805_127970173 | MFSD8 | chr4 | 127912805 | 127970173 |
| HG01517 | hp2 | a0001 | c0001 | t0001 | g0015 | EUR | IBS | MFSD8_chr4_127912805_127970173 | MFSD8 | chr4 | 127912805 | 127970173 |
| HG01884 | hp1 | a0001 | c0001 | t0001 | g0211 | AFR | ACB | MFSD8_chr4_127912805_127970173 | MFSD8 | chr4 | 127912805 | 127970173 |
| HG01884 | hp2 | a0001 | c0001 | t0001 | g0162 | AFR | ACB | MFSD8_chr4_127912805_127970173 | MFSD8 | chr4 | 127912805 | 127970173 |
| HG01891 | hp1 | a0001 | c0001 | t0001 | g0153 | AFR | ACB | MFSD8_chr4_127912805_127970173 | MFSD8 | chr4 | 127912805 | 127970173 |
| HG01891 | hp2 | a0002 | c0002 | t0006 | g0091 | AFR | ACB | MFSD8_chr4_127912805_127970173 | MFSD8 | chr4 | 127912805 | 127970173 |
| HG01943 | hp1 | a0001 | c0001 | t0001 | g0013 | AMR | PEL | MFSD8_chr4_127912805_127970173 | MFSD8 | chr4 | 127912805 | 127970173 |
| HG01943 | hp2 | a0003 | c0003 | t0009 | g0172 | AMR | PEL | MFSD8_chr4_127912805_127970173 | MFSD8 | chr4 | 127912805 | 127970173 |
| HG01952 | hp1 | a0001 | c0001 | t0001 | g0127 | AMR | PEL | MFSD8_chr4_127912805_127970173 | MFSD8 | chr4 | 127912805 | 127970173 |
| HG01952 | hp2 | a0003 | c0003 | t0009 | g0140 | AMR | PEL | MFSD8_chr4_127912805_127970173 | MFSD8 | chr4 | 127912805 | 127970173 |
| HG01978 | hp1 | a0003 | c0003 | t0001 | g0139 | AMR | PEL | MFSD8_chr4_127912805_127970173 | MFSD8 | chr4 | 127912805 | 127970173 |
| HG01978 | hp2 | a0002 | c0002 | t0002 | g0084 | AMR | PEL | MFSD8_chr4_127912805_127970173 | MFSD8 | chr4 | 127912805 | 127970173 |
| HG01981 | hp1 | a0001 | c0001 | t0001 | g0220 | AMR | PEL | MFSD8_chr4_127912805_127970173 | MFSD8 | chr4 | 127912805 | 127970173 |
| HG01981 | hp2 | a0002 | c0002 | t0002 | g0056 | AMR | PEL | MFSD8_chr4_127912805_127970173 | MFSD8 | chr4 | 127912805 | 127970173 |
| HG02015 | hp1 | a0001 | c0001 | t0001 | g0273 | EAS | KHV | MFSD8_chr4_127912805_127970173 | MFSD8 | chr4 | 127912805 | 127970173 |
| HG02015 | hp2 | a0001 | c0001 | t0001 | g0180 | EAS | KHV | MFSD8_chr4_127912805_127970173 | MFSD8 | chr4 | 127912805 | 127970173 |
| HG02027 | hp1 | a0001 | c0001 | t0001 | g0132 | EAS | KHV | MFSD8_chr4_127912805_127970173 | MFSD8 | chr4 | 127912805 | 127970173 |
| HG02027 | hp2 | a0001 | c0001 | t0019 | g0233 | EAS | KHV | MFSD8_chr4_127912805_127970173 | MFSD8 | chr4 | 127912805 | 127970173 |
| HG02055 | hp1 | a0001 | c0001 | t0001 | g0210 | AFR | ACB | MFSD8_chr4_127912805_127970173 | MFSD8 | chr4 | 127912805 | 127970173 |
| HG02055 | hp2 | a0002 | c0002 | t0005 | g0313 | AFR | ACB | MFSD8_chr4_127912805_127970173 | MFSD8 | chr4 | 127912805 | 127970173 |
| HG02056 | hp1 | a0002 | c0002 | t0002 | g0029 | EAS | KHV | MFSD8_chr4_127912805_127970173 | MFSD8 | chr4 | 127912805 | 127970173 |
| HG02056 | hp2 | a0003 | c0003 | t0021 | g0154 | EAS | KHV | MFSD8_chr4_127912805_127970173 | MFSD8 | chr4 | 127912805 | 127970173 |
| HG02071 | hp1 | a0001 | c0001 | t0001 | g0274 | EAS | KHV | MFSD8_chr4_127912805_127970173 | MFSD8 | chr4 | 127912805 | 127970173 |
| HG02071 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | MFSD8_chr4_127912805_127970173 | MFSD8 | chr4 | 127912805 | 127970173 |
| HG02074 | hp1 | a0002 | c0002 | t0002 | g0083 | EAS | KHV | MFSD8_chr4_127912805_127970173 | MFSD8 | chr4 | 127912805 | 127970173 |
| HG02074 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | KHV | MFSD8_chr4_127912805_127970173 | MFSD8 | chr4 | 127912805 | 127970173 |
| HG02080 | hp1 | a0001 | c0001 | t0001 | g0191 | EAS | KHV | MFSD8_chr4_127912805_127970173 | MFSD8 | chr4 | 127912805 | 127970173 |
| HG02080 | hp2 | a0001 | c0001 | t0001 | g0261 | EAS | KHV | MFSD8_chr4_127912805_127970173 | MFSD8 | chr4 | 127912805 | 127970173 |
| HG02083 | hp1 | a0001 | c0001 | t0001 | g0214 | EAS | KHV | MFSD8_chr4_127912805_127970173 | MFSD8 | chr4 | 127912805 | 127970173 |
| HG02083 | hp2 | a0001 | c0001 | t0017 | g0159 | EAS | KHV | MFSD8_chr4_127912805_127970173 | MFSD8 | chr4 | 127912805 | 127970173 |
| HG02132 | hp1 | a0002 | c0002 | t0002 | g0069 | EAS | KHV | MFSD8_chr4_127912805_127970173 | MFSD8 | chr4 | 127912805 | 127970173 |
| HG02132 | hp2 | a0003 | c0003 | t0001 | g0163 | EAS | KHV | MFSD8_chr4_127912805_127970173 | MFSD8 | chr4 | 127912805 | 127970173 |
| HG02155 | hp1 | a0001 | c0001 | t0001 | g0024 | EAS | CDX | MFSD8_chr4_127912805_127970173 | MFSD8 | chr4 | 127912805 | 127970173 |
| HG02155 | hp2 | a0001 | c0001 | t0001 | g0184 | EAS | CDX | MFSD8_chr4_127912805_127970173 | MFSD8 | chr4 | 127912805 | 127970173 |
| HG02165 | hp1 | a0001 | c0001 | t0001 | g0158 | EAS | CDX | MFSD8_chr4_127912805_127970173 | MFSD8 | chr4 | 127912805 | 127970173 |
| HG02165 | hp2 | a0001 | c0001 | t0001 | g0275 | EAS | CDX | MFSD8_chr4_127912805_127970173 | MFSD8 | chr4 | 127912805 | 127970173 |
| HG02257 | hp1 | a0001 | c0001 | t0001 | g0169 | AFR | ACB | MFSD8_chr4_127912805_127970173 | MFSD8 | chr4 | 127912805 | 127970173 |
| HG02257 | hp2 | a0002 | c0002 | t0003 | g0093 | AFR | ACB | MFSD8_chr4_127912805_127970173 | MFSD8 | chr4 | 127912805 | 127970173 |
| HG02258 | hp1 | a0001 | c0001 | t0001 | g0229 | AFR | ACB | MFSD8_chr4_127912805_127970173 | MFSD8 | chr4 | 127912805 | 127970173 |
| HG02258 | hp2 | a0001 | c0001 | t0001 | g0108 | AFR | ACB | MFSD8_chr4_127912805_127970173 | MFSD8 | chr4 | 127912805 | 127970173 |
| HG02273 | hp1 | a0001 | c0001 | t0001 | g0125 | AMR | PEL | MFSD8_chr4_127912805_127970173 | MFSD8 | chr4 | 127912805 | 127970173 |
| HG02273 | hp2 | a0002 | c0002 | t0002 | g0050 | AMR | PEL | MFSD8_chr4_127912805_127970173 | MFSD8 | chr4 | 127912805 | 127970173 |
| HG02280 | hp1 | a0001 | c0001 | t0001 | g0120 | AFR | ACB | MFSD8_chr4_127912805_127970173 | MFSD8 | chr4 | 127912805 | 127970173 |
| HG02280 | hp2 | a0001 | c0001 | t0022 | g0309 | AFR | ACB | MFSD8_chr4_127912805_127970173 | MFSD8 | chr4 | 127912805 | 127970173 |
| HG02300 | hp1 | a0001 | c0001 | t0001 | g0194 | AMR | PEL | MFSD8_chr4_127912805_127970173 | MFSD8 | chr4 | 127912805 | 127970173 |
| HG02300 | hp2 | a0002 | c0002 | t0002 | g0004 | AMR | PEL | MFSD8_chr4_127912805_127970173 | MFSD8 | chr4 | 127912805 | 127970173 |
| HG02451 | hp1 | a0001 | c0009 | t0014 | g0310 | AFR | ACB | MFSD8_chr4_127912805_127970173 | MFSD8 | chr4 | 127912805 | 127970173 |
| HG02451 | hp2 | a0002 | c0002 | t0003 | g0095 | AFR | ACB | MFSD8_chr4_127912805_127970173 | MFSD8 | chr4 | 127912805 | 127970173 |
| HG02523 | hp1 | a0001 | c0001 | t0001 | g0105 | EAS | KHV | MFSD8_chr4_127912805_127970173 | MFSD8 | chr4 | 127912805 | 127970173 |
| HG02523 | hp2 | a0002 | c0002 | t0002 | g0065 | EAS | KHV | MFSD8_chr4_127912805_127970173 | MFSD8 | chr4 | 127912805 | 127970173 |
| HG02572 | hp1 | a0004 | c0004 | t0005 | g0092 | AFR | GWD | MFSD8_chr4_127912805_127970173 | MFSD8 | chr4 | 127912805 | 127970173 |
| HG02572 | hp2 | a0001 | c0001 | t0001 | g0267 | AFR | GWD | MFSD8_chr4_127912805_127970173 | MFSD8 | chr4 | 127912805 | 127970173 |
| HG02602 | hp1 | a0001 | c0001 | t0001 | g0258 | SAS | PJL | MFSD8_chr4_127912805_127970173 | MFSD8 | chr4 | 127912805 | 127970173 |
| HG02602 | hp2 | a0001 | c0001 | t0001 | g0142 | SAS | PJL | MFSD8_chr4_127912805_127970173 | MFSD8 | chr4 | 127912805 | 127970173 |
| HG02615 | hp1 | a0001 | c0001 | t0001 | g0219 | AFR | GWD | MFSD8_chr4_127912805_127970173 | MFSD8 | chr4 | 127912805 | 127970173 |
| HG02615 | hp2 | a0001 | c0001 | t0001 | g0222 | AFR | GWD | MFSD8_chr4_127912805_127970173 | MFSD8 | chr4 | 127912805 | 127970173 |
| HG02622 | hp1 | a0001 | c0001 | t0001 | g0014 | AFR | GWD | MFSD8_chr4_127912805_127970173 | MFSD8 | chr4 | 127912805 | 127970173 |
| HG02622 | hp2 | a0002 | c0002 | t0006 | g0306 | AFR | GWD | MFSD8_chr4_127912805_127970173 | MFSD8 | chr4 | 127912805 | 127970173 |
| HG02630 | hp1 | a0001 | c0001 | t0001 | g0149 | AFR | GWD | MFSD8_chr4_127912805_127970173 | MFSD8 | chr4 | 127912805 | 127970173 |
| HG02630 | hp2 | a0002 | c0002 | t0003 | g0098 | AFR | GWD | MFSD8_chr4_127912805_127970173 | MFSD8 | chr4 | 127912805 | 127970173 |
| HG02647 | hp1 | a0001 | c0001 | t0001 | g0012 | AFR | GWD | MFSD8_chr4_127912805_127970173 | MFSD8 | chr4 | 127912805 | 127970173 |
| HG02647 | hp2 | a0001 | c0001 | t0001 | g0209 | AFR | GWD | MFSD8_chr4_127912805_127970173 | MFSD8 | chr4 | 127912805 | 127970173 |
| HG02698 | hp1 | a0001 | c0001 | t0001 | g0256 | SAS | PJL | MFSD8_chr4_127912805_127970173 | MFSD8 | chr4 | 127912805 | 127970173 |
| HG02698 | hp2 | a0001 | c0001 | t0001 | g0294 | SAS | PJL | MFSD8_chr4_127912805_127970173 | MFSD8 | chr4 | 127912805 | 127970173 |
| HG02717 | hp1 | a0001 | c0001 | t0001 | g0315 | AFR | GWD | MFSD8_chr4_127912805_127970173 | MFSD8 | chr4 | 127912805 | 127970173 |
| HG02717 | hp2 | a0001 | c0001 | t0015 | g0112 | AFR | GWD | MFSD8_chr4_127912805_127970173 | MFSD8 | chr4 | 127912805 | 127970173 |
| HG02723 | hp1 | a0001 | c0001 | t0001 | g0225 | AFR | GWD | MFSD8_chr4_127912805_127970173 | MFSD8 | chr4 | 127912805 | 127970173 |
| HG02723 | hp2 | a0001 | c0001 | t0001 | g0260 | AFR | GWD | MFSD8_chr4_127912805_127970173 | MFSD8 | chr4 | 127912805 | 127970173 |
| HG02735 | hp1 | a0001 | c0005 | t0001 | g0103 | SAS | PJL | MFSD8_chr4_127912805_127970173 | MFSD8 | chr4 | 127912805 | 127970173 |
| HG02735 | hp2 | a0001 | c0001 | t0001 | g0186 | SAS | PJL | MFSD8_chr4_127912805_127970173 | MFSD8 | chr4 | 127912805 | 127970173 |
| HG02809 | hp1 | a0002 | c0002 | t0003 | g0100 | AFR | GWD | MFSD8_chr4_127912805_127970173 | MFSD8 | chr4 | 127912805 | 127970173 |
| HG02809 | hp2 | a0001 | c0001 | t0001 | g0236 | AFR | GWD | MFSD8_chr4_127912805_127970173 | MFSD8 | chr4 | 127912805 | 127970173 |
| HG02818 | hp1 | a0002 | c0002 | t0003 | g0102 | AFR | GWD | MFSD8_chr4_127912805_127970173 | MFSD8 | chr4 | 127912805 | 127970173 |
| HG02818 | hp2 | a0001 | c0001 | t0001 | g0023 | AFR | GWD | MFSD8_chr4_127912805_127970173 | MFSD8 | chr4 | 127912805 | 127970173 |
| HG02886 | hp1 | a0002 | c0002 | t0003 | g0097 | AFR | GWD | MFSD8_chr4_127912805_127970173 | MFSD8 | chr4 | 127912805 | 127970173 |
| HG02886 | hp2 | a0001 | c0001 | t0001 | g0114 | AFR | GWD | MFSD8_chr4_127912805_127970173 | MFSD8 | chr4 | 127912805 | 127970173 |
| HG02896 | hp1 | a0001 | c0001 | t0001 | g0259 | AFR | GWD | MFSD8_chr4_127912805_127970173 | MFSD8 | chr4 | 127912805 | 127970173 |
| HG02896 | hp2 | a0001 | c0001 | t0001 | g0113 | AFR | GWD | MFSD8_chr4_127912805_127970173 | MFSD8 | chr4 | 127912805 | 127970173 |
| HG02897 | hp1 | a0001 | c0001 | t0001 | g0150 | AFR | GWD | MFSD8_chr4_127912805_127970173 | MFSD8 | chr4 | 127912805 | 127970173 |
| HG02897 | hp2 | a0001 | c0001 | t0001 | g0218 | AFR | GWD | MFSD8_chr4_127912805_127970173 | MFSD8 | chr4 | 127912805 | 127970173 |
| HG02922 | hp1 | a0001 | c0001 | t0001 | g0119 | AFR | ESN | MFSD8_chr4_127912805_127970173 | MFSD8 | chr4 | 127912805 | 127970173 |
| HG02922 | hp2 | a0004 | c0004 | t0010 | g0011 | AFR | ESN | MFSD8_chr4_127912805_127970173 | MFSD8 | chr4 | 127912805 | 127970173 |
| HG02965 | hp1 | a0001 | c0001 | t0001 | g0022 | AFR | ESN | MFSD8_chr4_127912805_127970173 | MFSD8 | chr4 | 127912805 | 127970173 |
| HG02965 | hp2 | a0001 | c0001 | t0001 | g0111 | AFR | ESN | MFSD8_chr4_127912805_127970173 | MFSD8 | chr4 | 127912805 | 127970173 |
| HG02970 | hp1 | a0001 | c0001 | t0001 | g0307 | AFR | ESN | MFSD8_chr4_127912805_127970173 | MFSD8 | chr4 | 127912805 | 127970173 |
| HG02970 | hp2 | a0001 | c0001 | t0001 | g0018 | AFR | ESN | MFSD8_chr4_127912805_127970173 | MFSD8 | chr4 | 127912805 | 127970173 |
| HG02976 | hp1 | a0002 | c0002 | t0005 | g0312 | AFR | ESN | MFSD8_chr4_127912805_127970173 | MFSD8 | chr4 | 127912805 | 127970173 |
| HG02976 | hp2 | a0001 | c0001 | t0001 | g0235 | AFR | ESN | MFSD8_chr4_127912805_127970173 | MFSD8 | chr4 | 127912805 | 127970173 |
| HG03017 | hp1 | a0001 | c0001 | t0001 | g0170 | SAS | PJL | MFSD8_chr4_127912805_127970173 | MFSD8 | chr4 | 127912805 | 127970173 |
| HG03017 | hp2 | a0001 | c0005 | t0001 | g0104 | SAS | PJL | MFSD8_chr4_127912805_127970173 | MFSD8 | chr4 | 127912805 | 127970173 |
| HG03041 | hp1 | a0001 | c0001 | t0001 | g0289 | AFR | GWD | MFSD8_chr4_127912805_127970173 | MFSD8 | chr4 | 127912805 | 127970173 |
| HG03041 | hp2 | a0001 | c0001 | t0001 | g0223 | AFR | GWD | MFSD8_chr4_127912805_127970173 | MFSD8 | chr4 | 127912805 | 127970173 |
| HG03098 | hp1 | a0001 | c0001 | t0001 | g0227 | AFR | MSL | MFSD8_chr4_127912805_127970173 | MFSD8 | chr4 | 127912805 | 127970173 |
| HG03098 | hp2 | a0001 | c0001 | t0001 | g0110 | AFR | MSL | MFSD8_chr4_127912805_127970173 | MFSD8 | chr4 | 127912805 | 127970173 |
| HG03130 | hp1 | a0001 | c0001 | t0001 | g0257 | AFR | ESN | MFSD8_chr4_127912805_127970173 | MFSD8 | chr4 | 127912805 | 127970173 |
| HG03130 | hp2 | a0001 | c0001 | t0001 | g0130 | AFR | ESN | MFSD8_chr4_127912805_127970173 | MFSD8 | chr4 | 127912805 | 127970173 |
| HG03139 | hp1 | a0001 | c0001 | t0018 | g0196 | AFR | ESN | MFSD8_chr4_127912805_127970173 | MFSD8 | chr4 | 127912805 | 127970173 |
| HG03139 | hp2 | a0001 | c0001 | t0001 | g0305 | AFR | ESN | MFSD8_chr4_127912805_127970173 | MFSD8 | chr4 | 127912805 | 127970173 |
| HG03195 | hp1 | a0001 | c0001 | t0001 | g0262 | AFR | ESN | MFSD8_chr4_127912805_127970173 | MFSD8 | chr4 | 127912805 | 127970173 |
| HG03195 | hp2 | a0001 | c0001 | t0001 | g0116 | AFR | ESN | MFSD8_chr4_127912805_127970173 | MFSD8 | chr4 | 127912805 | 127970173 |
| HG03209 | hp1 | a0001 | c0001 | t0001 | g0018 | AFR | MSL | MFSD8_chr4_127912805_127970173 | MFSD8 | chr4 | 127912805 | 127970173 |
| HG03209 | hp2 | a0002 | c0002 | t0005 | g0314 | AFR | MSL | MFSD8_chr4_127912805_127970173 | MFSD8 | chr4 | 127912805 | 127970173 |
| HG03225 | hp1 | a0002 | c0002 | t0006 | g0089 | AFR | MSL | MFSD8_chr4_127912805_127970173 | MFSD8 | chr4 | 127912805 | 127970173 |
| HG03225 | hp2 | a0001 | c0001 | t0001 | g0193 | AFR | MSL | MFSD8_chr4_127912805_127970173 | MFSD8 | chr4 | 127912805 | 127970173 |
| HG03453 | hp1 | a0005 | c0007 | t0001 | g0157 | AFR | MSL | MFSD8_chr4_127912805_127970173 | MFSD8 | chr4 | 127912805 | 127970173 |
| HG03453 | hp2 | a0001 | c0001 | t0001 | g0118 | AFR | MSL | MFSD8_chr4_127912805_127970173 | MFSD8 | chr4 | 127912805 | 127970173 |
| HG03486 | hp1 | a0001 | c0001 | t0001 | g0237 | AFR | MSL | MFSD8_chr4_127912805_127970173 | MFSD8 | chr4 | 127912805 | 127970173 |
| HG03486 | hp2 | a0001 | c0001 | t0001 | g0107 | AFR | MSL | MFSD8_chr4_127912805_127970173 | MFSD8 | chr4 | 127912805 | 127970173 |
| HG03490 | hp1 | a0001 | c0001 | t0001 | g0014 | SAS | PJL | MFSD8_chr4_127912805_127970173 | MFSD8 | chr4 | 127912805 | 127970173 |
| HG03490 | hp2 | a0001 | c0001 | t0001 | g0293 | SAS | PJL | MFSD8_chr4_127912805_127970173 | MFSD8 | chr4 | 127912805 | 127970173 |
| HG03516 | hp1 | a0001 | c0001 | t0001 | g0308 | AFR | ESN | MFSD8_chr4_127912805_127970173 | MFSD8 | chr4 | 127912805 | 127970173 |
| HG03516 | hp2 | a0001 | c0001 | t0001 | g0133 | AFR | ESN | MFSD8_chr4_127912805_127970173 | MFSD8 | chr4 | 127912805 | 127970173 |
| HG03540 | hp1 | a0002 | c0002 | t0003 | g0316 | AFR | GWD | MFSD8_chr4_127912805_127970173 | MFSD8 | chr4 | 127912805 | 127970173 |
| HG03540 | hp2 | a0001 | c0001 | t0001 | g0231 | AFR | GWD | MFSD8_chr4_127912805_127970173 | MFSD8 | chr4 | 127912805 | 127970173 |
| HG03579 | hp1 | a0002 | c0002 | t0003 | g0094 | AFR | MSL | MFSD8_chr4_127912805_127970173 | MFSD8 | chr4 | 127912805 | 127970173 |
| HG03579 | hp2 | a0001 | c0001 | t0001 | g0141 | AFR | MSL | MFSD8_chr4_127912805_127970173 | MFSD8 | chr4 | 127912805 | 127970173 |
| HG03669 | hp1 | a0001 | c0001 | t0001 | g0212 | SAS | PJL | MFSD8_chr4_127912805_127970173 | MFSD8 | chr4 | 127912805 | 127970173 |
| HG03669 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | MFSD8_chr4_127912805_127970173 | MFSD8 | chr4 | 127912805 | 127970173 |
| HG03688 | hp1 | a0001 | c0001 | t0001 | g0006 | SAS | STU | MFSD8_chr4_127912805_127970173 | MFSD8 | chr4 | 127912805 | 127970173 |
| HG03688 | hp2 | a0001 | c0001 | t0001 | g0297 | SAS | STU | MFSD8_chr4_127912805_127970173 | MFSD8 | chr4 | 127912805 | 127970173 |
| HG03704 | hp1 | a0001 | c0001 | t0001 | g0175 | SAS | PJL | MFSD8_chr4_127912805_127970173 | MFSD8 | chr4 | 127912805 | 127970173 |
| HG03704 | hp2 | a0001 | c0001 | t0001 | g0221 | SAS | PJL | MFSD8_chr4_127912805_127970173 | MFSD8 | chr4 | 127912805 | 127970173 |
| HG03710 | hp1 | a0001 | c0001 | t0001 | g0156 | SAS | PJL | MFSD8_chr4_127912805_127970173 | MFSD8 | chr4 | 127912805 | 127970173 |
| HG03710 | hp2 | a0001 | c0001 | t0001 | g0239 | SAS | PJL | MFSD8_chr4_127912805_127970173 | MFSD8 | chr4 | 127912805 | 127970173 |
| HG03834 | hp1 | a0001 | c0001 | t0001 | g0248 | SAS | BEB | MFSD8_chr4_127912805_127970173 | MFSD8 | chr4 | 127912805 | 127970173 |
| HG03834 | hp2 | a0001 | c0001 | t0001 | g0187 | SAS | BEB | MFSD8_chr4_127912805_127970173 | MFSD8 | chr4 | 127912805 | 127970173 |
| HG04115 | hp1 | a0001 | c0001 | t0001 | g0202 | SAS | STU | MFSD8_chr4_127912805_127970173 | MFSD8 | chr4 | 127912805 | 127970173 |
| HG04115 | hp2 | a0001 | c0001 | t0001 | g0005 | SAS | STU | MFSD8_chr4_127912805_127970173 | MFSD8 | chr4 | 127912805 | 127970173 |
| HG04184 | hp1 | a0001 | c0001 | t0001 | g0300 | SAS | BEB | MFSD8_chr4_127912805_127970173 | MFSD8 | chr4 | 127912805 | 127970173 |
| HG04184 | hp2 | a0001 | c0001 | t0001 | g0188 | SAS | BEB | MFSD8_chr4_127912805_127970173 | MFSD8 | chr4 | 127912805 | 127970173 |
| HG04199 | hp1 | a0001 | c0001 | t0001 | g0288 | SAS | STU | MFSD8_chr4_127912805_127970173 | MFSD8 | chr4 | 127912805 | 127970173 |
| HG04199 | hp2 | a0001 | c0001 | t0001 | g0005 | SAS | STU | MFSD8_chr4_127912805_127970173 | MFSD8 | chr4 | 127912805 | 127970173 |
| HG04204 | hp1 | a0001 | c0001 | t0001 | g0164 | SAS | STU | MFSD8_chr4_127912805_127970173 | MFSD8 | chr4 | 127912805 | 127970173 |
| HG04204 | hp2 | a0001 | c0001 | t0001 | g0124 | SAS | STU | MFSD8_chr4_127912805_127970173 | MFSD8 | chr4 | 127912805 | 127970173 |
| HG04228 | hp1 | a0001 | c0001 | t0001 | g0161 | SAS | STU | MFSD8_chr4_127912805_127970173 | MFSD8 | chr4 | 127912805 | 127970173 |
| HG04228 | hp2 | a0001 | c0001 | t0001 | g0160 | SAS | STU | MFSD8_chr4_127912805_127970173 | MFSD8 | chr4 | 127912805 | 127970173 |
| NA18747 | hp1 | a0001 | c0001 | t0001 | g0026 | EAS | CHB | MFSD8_chr4_127912805_127970173 | MFSD8 | chr4 | 127912805 | 127970173 |
| NA18747 | hp2 | a0002 | c0002 | t0002 | g0009 | EAS | CHB | MFSD8_chr4_127912805_127970173 | MFSD8 | chr4 | 127912805 | 127970173 |
| NA18906 | hp1 | a0002 | c0002 | t0003 | g0101 | AFR | YRI | MFSD8_chr4_127912805_127970173 | MFSD8 | chr4 | 127912805 | 127970173 |
| NA18906 | hp2 | a0001 | c0001 | t0001 | g0226 | AFR | YRI | MFSD8_chr4_127912805_127970173 | MFSD8 | chr4 | 127912805 | 127970173 |
| NA18939 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | MFSD8_chr4_127912805_127970173 | MFSD8 | chr4 | 127912805 | 127970173 |
| NA18939 | hp2 | a0002 | c0002 | t0002 | g0057 | EAS | JPT | MFSD8_chr4_127912805_127970173 | MFSD8 | chr4 | 127912805 | 127970173 |
| NA18942 | hp1 | a0001 | c0001 | t0001 | g0121 | EAS | JPT | MFSD8_chr4_127912805_127970173 | MFSD8 | chr4 | 127912805 | 127970173 |
| NA18942 | hp2 | a0002 | c0002 | t0002 | g0008 | EAS | JPT | MFSD8_chr4_127912805_127970173 | MFSD8 | chr4 | 127912805 | 127970173 |
| NA18943 | hp1 | a0001 | c0001 | t0001 | g0143 | EAS | JPT | MFSD8_chr4_127912805_127970173 | MFSD8 | chr4 | 127912805 | 127970173 |
| NA18943 | hp2 | a0002 | c0002 | t0002 | g0045 | EAS | JPT | MFSD8_chr4_127912805_127970173 | MFSD8 | chr4 | 127912805 | 127970173 |
| NA18945 | hp1 | a0001 | c0001 | t0001 | g0285 | EAS | JPT | MFSD8_chr4_127912805_127970173 | MFSD8 | chr4 | 127912805 | 127970173 |
| NA18945 | hp2 | a0001 | c0001 | t0001 | g0192 | EAS | JPT | MFSD8_chr4_127912805_127970173 | MFSD8 | chr4 | 127912805 | 127970173 |
| NA18946 | hp1 | a0002 | c0002 | t0004 | g0063 | EAS | JPT | MFSD8_chr4_127912805_127970173 | MFSD8 | chr4 | 127912805 | 127970173 |
| NA18946 | hp2 | a0001 | c0001 | t0001 | g0183 | EAS | JPT | MFSD8_chr4_127912805_127970173 | MFSD8 | chr4 | 127912805 | 127970173 |
| NA18947 | hp1 | a0002 | c0002 | t0002 | g0062 | EAS | JPT | MFSD8_chr4_127912805_127970173 | MFSD8 | chr4 | 127912805 | 127970173 |
| NA18947 | hp2 | a0001 | c0001 | t0001 | g0265 | EAS | JPT | MFSD8_chr4_127912805_127970173 | MFSD8 | chr4 | 127912805 | 127970173 |
| NA18948 | hp1 | a0003 | c0003 | t0001 | g0016 | EAS | JPT | MFSD8_chr4_127912805_127970173 | MFSD8 | chr4 | 127912805 | 127970173 |
| NA18948 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | MFSD8_chr4_127912805_127970173 | MFSD8 | chr4 | 127912805 | 127970173 |
| NA18949 | hp1 | a0001 | c0001 | t0001 | g0206 | EAS | JPT | MFSD8_chr4_127912805_127970173 | MFSD8 | chr4 | 127912805 | 127970173 |
| NA18949 | hp2 | a0001 | c0001 | t0008 | g0244 | EAS | JPT | MFSD8_chr4_127912805_127970173 | MFSD8 | chr4 | 127912805 | 127970173 |
| NA18950 | hp1 | a0001 | c0001 | t0001 | g0017 | EAS | JPT | MFSD8_chr4_127912805_127970173 | MFSD8 | chr4 | 127912805 | 127970173 |
| NA18950 | hp2 | a0001 | c0001 | t0007 | g0007 | EAS | JPT | MFSD8_chr4_127912805_127970173 | MFSD8 | chr4 | 127912805 | 127970173 |
| NA18951 | hp1 | a0002 | c0002 | t0002 | g0052 | EAS | JPT | MFSD8_chr4_127912805_127970173 | MFSD8 | chr4 | 127912805 | 127970173 |
| NA18951 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | MFSD8_chr4_127912805_127970173 | MFSD8 | chr4 | 127912805 | 127970173 |
| NA18952 | hp1 | a0002 | c0002 | t0002 | g0087 | EAS | JPT | MFSD8_chr4_127912805_127970173 | MFSD8 | chr4 | 127912805 | 127970173 |
| NA18952 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | MFSD8_chr4_127912805_127970173 | MFSD8 | chr4 | 127912805 | 127970173 |
| NA18954 | hp1 | a0001 | c0001 | t0001 | g0020 | EAS | JPT | MFSD8_chr4_127912805_127970173 | MFSD8 | chr4 | 127912805 | 127970173 |
| NA18954 | hp2 | a0002 | c0002 | t0002 | g0066 | EAS | JPT | MFSD8_chr4_127912805_127970173 | MFSD8 | chr4 | 127912805 | 127970173 |
| NA18956 | hp1 | a0001 | c0001 | t0001 | g0282 | EAS | JPT | MFSD8_chr4_127912805_127970173 | MFSD8 | chr4 | 127912805 | 127970173 |
| NA18956 | hp2 | a0002 | c0002 | t0002 | g0072 | EAS | JPT | MFSD8_chr4_127912805_127970173 | MFSD8 | chr4 | 127912805 | 127970173 |
| NA18957 | hp1 | a0001 | c0001 | t0001 | g0020 | EAS | JPT | MFSD8_chr4_127912805_127970173 | MFSD8 | chr4 | 127912805 | 127970173 |
| NA18957 | hp2 | a0002 | c0002 | t0002 | g0064 | EAS | JPT | MFSD8_chr4_127912805_127970173 | MFSD8 | chr4 | 127912805 | 127970173 |
| NA18959 | hp1 | a0001 | c0001 | t0001 | g0203 | EAS | JPT | MFSD8_chr4_127912805_127970173 | MFSD8 | chr4 | 127912805 | 127970173 |
| NA18959 | hp2 | a0001 | c0001 | t0001 | g0234 | EAS | JPT | MFSD8_chr4_127912805_127970173 | MFSD8 | chr4 | 127912805 | 127970173 |
| NA18960 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | MFSD8_chr4_127912805_127970173 | MFSD8 | chr4 | 127912805 | 127970173 |
| NA18960 | hp2 | a0002 | c0002 | t0002 | g0059 | EAS | JPT | MFSD8_chr4_127912805_127970173 | MFSD8 | chr4 | 127912805 | 127970173 |
| NA18961 | hp1 | a0001 | c0001 | t0001 | g0301 | EAS | JPT | MFSD8_chr4_127912805_127970173 | MFSD8 | chr4 | 127912805 | 127970173 |
| NA18961 | hp2 | a0002 | c0002 | t0002 | g0004 | EAS | JPT | MFSD8_chr4_127912805_127970173 | MFSD8 | chr4 | 127912805 | 127970173 |
| NA18962 | hp1 | a0002 | c0002 | t0002 | g0037 | EAS | JPT | MFSD8_chr4_127912805_127970173 | MFSD8 | chr4 | 127912805 | 127970173 |
| NA18962 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | MFSD8_chr4_127912805_127970173 | MFSD8 | chr4 | 127912805 | 127970173 |
| NA18966 | hp1 | a0002 | c0002 | t0002 | g0054 | EAS | JPT | MFSD8_chr4_127912805_127970173 | MFSD8 | chr4 | 127912805 | 127970173 |
| NA18966 | hp2 | a0001 | c0001 | t0001 | g0252 | EAS | JPT | MFSD8_chr4_127912805_127970173 | MFSD8 | chr4 | 127912805 | 127970173 |
| NA18968 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | MFSD8_chr4_127912805_127970173 | MFSD8 | chr4 | 127912805 | 127970173 |
| NA18968 | hp2 | a0002 | c0002 | t0002 | g0009 | EAS | JPT | MFSD8_chr4_127912805_127970173 | MFSD8 | chr4 | 127912805 | 127970173 |
| NA18969 | hp1 | a0001 | c0001 | t0001 | g0017 | EAS | JPT | MFSD8_chr4_127912805_127970173 | MFSD8 | chr4 | 127912805 | 127970173 |
| NA18969 | hp2 | a0001 | c0001 | t0001 | g0302 | EAS | JPT | MFSD8_chr4_127912805_127970173 | MFSD8 | chr4 | 127912805 | 127970173 |
| NA18970 | hp1 | a0002 | c0002 | t0002 | g0042 | EAS | JPT | MFSD8_chr4_127912805_127970173 | MFSD8 | chr4 | 127912805 | 127970173 |
| NA18970 | hp2 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | MFSD8_chr4_127912805_127970173 | MFSD8 | chr4 | 127912805 | 127970173 |
| NA18972 | hp1 | a0003 | c0003 | t0001 | g0148 | EAS | JPT | MFSD8_chr4_127912805_127970173 | MFSD8 | chr4 | 127912805 | 127970173 |
| NA18972 | hp2 | a0002 | c0002 | t0002 | g0031 | EAS | JPT | MFSD8_chr4_127912805_127970173 | MFSD8 | chr4 | 127912805 | 127970173 |
| NA18973 | hp1 | a0001 | c0001 | t0001 | g0182 | EAS | JPT | MFSD8_chr4_127912805_127970173 | MFSD8 | chr4 | 127912805 | 127970173 |
| NA18973 | hp2 | a0001 | c0001 | t0007 | g0007 | EAS | JPT | MFSD8_chr4_127912805_127970173 | MFSD8 | chr4 | 127912805 | 127970173 |
| NA18974 | hp1 | a0002 | c0002 | t0002 | g0070 | EAS | JPT | MFSD8_chr4_127912805_127970173 | MFSD8 | chr4 | 127912805 | 127970173 |
| NA18974 | hp2 | a0001 | c0001 | t0001 | g0185 | EAS | JPT | MFSD8_chr4_127912805_127970173 | MFSD8 | chr4 | 127912805 | 127970173 |
| NA18977 | hp1 | a0002 | c0002 | t0002 | g0032 | EAS | JPT | MFSD8_chr4_127912805_127970173 | MFSD8 | chr4 | 127912805 | 127970173 |
| NA18977 | hp2 | a0001 | c0001 | t0007 | g0027 | EAS | JPT | MFSD8_chr4_127912805_127970173 | MFSD8 | chr4 | 127912805 | 127970173 |
| NA18978 | hp1 | a0001 | c0001 | t0001 | g0281 | EAS | JPT | MFSD8_chr4_127912805_127970173 | MFSD8 | chr4 | 127912805 | 127970173 |
| NA18978 | hp2 | a0002 | c0002 | t0002 | g0074 | EAS | JPT | MFSD8_chr4_127912805_127970173 | MFSD8 | chr4 | 127912805 | 127970173 |
| NA18979 | hp1 | a0001 | c0001 | t0001 | g0276 | EAS | JPT | MFSD8_chr4_127912805_127970173 | MFSD8 | chr4 | 127912805 | 127970173 |
| NA18979 | hp2 | a0001 | c0001 | t0007 | g0028 | EAS | JPT | MFSD8_chr4_127912805_127970173 | MFSD8 | chr4 | 127912805 | 127970173 |
| NA18980 | hp1 | a0001 | c0001 | t0001 | g0287 | EAS | JPT | MFSD8_chr4_127912805_127970173 | MFSD8 | chr4 | 127912805 | 127970173 |
| NA18980 | hp2 | a0001 | c0001 | t0001 | g0311 | EAS | JPT | MFSD8_chr4_127912805_127970173 | MFSD8 | chr4 | 127912805 | 127970173 |
| NA18981 | hp1 | a0002 | c0002 | t0002 | g0010 | EAS | JPT | MFSD8_chr4_127912805_127970173 | MFSD8 | chr4 | 127912805 | 127970173 |
| NA18981 | hp2 | a0001 | c0001 | t0001 | g0272 | EAS | JPT | MFSD8_chr4_127912805_127970173 | MFSD8 | chr4 | 127912805 | 127970173 |
| NA18983 | hp1 | a0002 | c0002 | t0002 | g0078 | EAS | JPT | MFSD8_chr4_127912805_127970173 | MFSD8 | chr4 | 127912805 | 127970173 |
| NA18983 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | MFSD8_chr4_127912805_127970173 | MFSD8 | chr4 | 127912805 | 127970173 |
| NA18984 | hp1 | a0002 | c0002 | t0002 | g0040 | EAS | JPT | MFSD8_chr4_127912805_127970173 | MFSD8 | chr4 | 127912805 | 127970173 |
| NA18984 | hp2 | a0001 | c0001 | t0001 | g0117 | EAS | JPT | MFSD8_chr4_127912805_127970173 | MFSD8 | chr4 | 127912805 | 127970173 |
| NA18985 | hp1 | a0001 | c0001 | t0001 | g0215 | EAS | JPT | MFSD8_chr4_127912805_127970173 | MFSD8 | chr4 | 127912805 | 127970173 |
| NA18985 | hp2 | a0003 | c0003 | t0001 | g0174 | EAS | JPT | MFSD8_chr4_127912805_127970173 | MFSD8 | chr4 | 127912805 | 127970173 |
| NA18986 | hp1 | a0007 | c0010 | t0002 | g0075 | EAS | JPT | MFSD8_chr4_127912805_127970173 | MFSD8 | chr4 | 127912805 | 127970173 |
| NA18986 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | MFSD8_chr4_127912805_127970173 | MFSD8 | chr4 | 127912805 | 127970173 |
| NA18987 | hp1 | a0001 | c0001 | t0001 | g0253 | EAS | JPT | MFSD8_chr4_127912805_127970173 | MFSD8 | chr4 | 127912805 | 127970173 |
| NA18987 | hp2 | a0001 | c0001 | t0011 | g0216 | EAS | JPT | MFSD8_chr4_127912805_127970173 | MFSD8 | chr4 | 127912805 | 127970173 |
| NA18988 | hp1 | a0001 | c0001 | t0001 | g0283 | EAS | JPT | MFSD8_chr4_127912805_127970173 | MFSD8 | chr4 | 127912805 | 127970173 |
| NA18988 | hp2 | a0002 | c0002 | t0002 | g0067 | EAS | JPT | MFSD8_chr4_127912805_127970173 | MFSD8 | chr4 | 127912805 | 127970173 |
| NA18994 | hp1 | a0003 | c0003 | t0001 | g0165 | EAS | JPT | MFSD8_chr4_127912805_127970173 | MFSD8 | chr4 | 127912805 | 127970173 |
| NA18994 | hp2 | a0002 | c0002 | t0002 | g0036 | EAS | JPT | MFSD8_chr4_127912805_127970173 | MFSD8 | chr4 | 127912805 | 127970173 |
| NA18998 | hp1 | a0001 | c0001 | t0011 | g0217 | EAS | JPT | MFSD8_chr4_127912805_127970173 | MFSD8 | chr4 | 127912805 | 127970173 |
| NA18998 | hp2 | a0001 | c0001 | t0001 | g0181 | EAS | JPT | MFSD8_chr4_127912805_127970173 | MFSD8 | chr4 | 127912805 | 127970173 |
| NA18999 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | MFSD8_chr4_127912805_127970173 | MFSD8 | chr4 | 127912805 | 127970173 |
| NA18999 | hp2 | a0002 | c0002 | t0002 | g0060 | EAS | JPT | MFSD8_chr4_127912805_127970173 | MFSD8 | chr4 | 127912805 | 127970173 |
| NA19000 | hp1 | a0002 | c0002 | t0002 | g0079 | EAS | JPT | MFSD8_chr4_127912805_127970173 | MFSD8 | chr4 | 127912805 | 127970173 |
| NA19000 | hp2 | a0001 | c0001 | t0001 | g0205 | EAS | JPT | MFSD8_chr4_127912805_127970173 | MFSD8 | chr4 | 127912805 | 127970173 |
| NA19001 | hp1 | a0002 | c0002 | t0002 | g0039 | EAS | JPT | MFSD8_chr4_127912805_127970173 | MFSD8 | chr4 | 127912805 | 127970173 |
| NA19001 | hp2 | a0001 | c0001 | t0001 | g0286 | EAS | JPT | MFSD8_chr4_127912805_127970173 | MFSD8 | chr4 | 127912805 | 127970173 |
| NA19002 | hp1 | a0001 | c0001 | t0001 | g0249 | EAS | JPT | MFSD8_chr4_127912805_127970173 | MFSD8 | chr4 | 127912805 | 127970173 |
| NA19002 | hp2 | a0002 | c0002 | t0002 | g0038 | EAS | JPT | MFSD8_chr4_127912805_127970173 | MFSD8 | chr4 | 127912805 | 127970173 |
| NA19005 | hp1 | a0002 | c0002 | t0023 | g0030 | EAS | JPT | MFSD8_chr4_127912805_127970173 | MFSD8 | chr4 | 127912805 | 127970173 |
| NA19005 | hp2 | a0001 | c0001 | t0001 | g0247 | EAS | JPT | MFSD8_chr4_127912805_127970173 | MFSD8 | chr4 | 127912805 | 127970173 |
| NA19007 | hp1 | a0002 | c0002 | t0002 | g0088 | EAS | JPT | MFSD8_chr4_127912805_127970173 | MFSD8 | chr4 | 127912805 | 127970173 |
| NA19007 | hp2 | a0001 | c0001 | t0001 | g0271 | EAS | JPT | MFSD8_chr4_127912805_127970173 | MFSD8 | chr4 | 127912805 | 127970173 |
| NA19009 | hp1 | a0002 | c0002 | t0002 | g0073 | EAS | JPT | MFSD8_chr4_127912805_127970173 | MFSD8 | chr4 | 127912805 | 127970173 |
| NA19009 | hp2 | a0001 | c0001 | t0001 | g0263 | EAS | JPT | MFSD8_chr4_127912805_127970173 | MFSD8 | chr4 | 127912805 | 127970173 |
| NA19011 | hp1 | a0002 | c0002 | t0002 | g0071 | EAS | JPT | MFSD8_chr4_127912805_127970173 | MFSD8 | chr4 | 127912805 | 127970173 |
| NA19011 | hp2 | a0001 | c0001 | t0001 | g0251 | EAS | JPT | MFSD8_chr4_127912805_127970173 | MFSD8 | chr4 | 127912805 | 127970173 |
| NA19012 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | MFSD8_chr4_127912805_127970173 | MFSD8 | chr4 | 127912805 | 127970173 |
| NA19012 | hp2 | a0001 | c0001 | t0001 | g0129 | EAS | JPT | MFSD8_chr4_127912805_127970173 | MFSD8 | chr4 | 127912805 | 127970173 |
| NA19030 | hp1 | a0001 | c0001 | t0001 | g0232 | AFR | LWK | MFSD8_chr4_127912805_127970173 | MFSD8 | chr4 | 127912805 | 127970173 |
| NA19030 | hp2 | a0001 | c0001 | t0001 | g0284 | AFR | LWK | MFSD8_chr4_127912805_127970173 | MFSD8 | chr4 | 127912805 | 127970173 |
| NA19054 | hp1 | a0001 | c0001 | t0001 | g0204 | EAS | JPT | MFSD8_chr4_127912805_127970173 | MFSD8 | chr4 | 127912805 | 127970173 |
| NA19054 | hp2 | a0002 | c0002 | t0002 | g0049 | EAS | JPT | MFSD8_chr4_127912805_127970173 | MFSD8 | chr4 | 127912805 | 127970173 |
| NA19056 | hp1 | a0002 | c0002 | t0002 | g0086 | EAS | JPT | MFSD8_chr4_127912805_127970173 | MFSD8 | chr4 | 127912805 | 127970173 |
| NA19056 | hp2 | a0003 | c0003 | t0001 | g0173 | EAS | JPT | MFSD8_chr4_127912805_127970173 | MFSD8 | chr4 | 127912805 | 127970173 |
| NA19057 | hp1 | a0001 | c0001 | t0001 | g0109 | EAS | JPT | MFSD8_chr4_127912805_127970173 | MFSD8 | chr4 | 127912805 | 127970173 |
| NA19057 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | MFSD8_chr4_127912805_127970173 | MFSD8 | chr4 | 127912805 | 127970173 |
| NA19062 | hp1 | a0002 | c0002 | t0002 | g0081 | EAS | JPT | MFSD8_chr4_127912805_127970173 | MFSD8 | chr4 | 127912805 | 127970173 |
| NA19062 | hp2 | a0001 | c0001 | t0008 | g0242 | EAS | JPT | MFSD8_chr4_127912805_127970173 | MFSD8 | chr4 | 127912805 | 127970173 |
| NA19063 | hp1 | a0001 | c0001 | t0001 | g0299 | EAS | JPT | MFSD8_chr4_127912805_127970173 | MFSD8 | chr4 | 127912805 | 127970173 |
| NA19063 | hp2 | a0002 | c0002 | t0002 | g0004 | EAS | JPT | MFSD8_chr4_127912805_127970173 | MFSD8 | chr4 | 127912805 | 127970173 |
| NA19065 | hp1 | a0002 | c0002 | t0002 | g0058 | EAS | JPT | MFSD8_chr4_127912805_127970173 | MFSD8 | chr4 | 127912805 | 127970173 |
| NA19065 | hp2 | a0001 | c0001 | t0001 | g0270 | EAS | JPT | MFSD8_chr4_127912805_127970173 | MFSD8 | chr4 | 127912805 | 127970173 |
| NA19066 | hp1 | a0001 | c0001 | t0001 | g0128 | EAS | JPT | MFSD8_chr4_127912805_127970173 | MFSD8 | chr4 | 127912805 | 127970173 |
| NA19066 | hp2 | a0002 | c0002 | t0002 | g0044 | EAS | JPT | MFSD8_chr4_127912805_127970173 | MFSD8 | chr4 | 127912805 | 127970173 |
| NA19068 | hp1 | a0002 | c0002 | t0002 | g0082 | EAS | JPT | MFSD8_chr4_127912805_127970173 | MFSD8 | chr4 | 127912805 | 127970173 |
| NA19068 | hp2 | a0003 | c0003 | t0001 | g0197 | EAS | JPT | MFSD8_chr4_127912805_127970173 | MFSD8 | chr4 | 127912805 | 127970173 |
| NA19070 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | MFSD8_chr4_127912805_127970173 | MFSD8 | chr4 | 127912805 | 127970173 |
| NA19070 | hp2 | a0002 | c0002 | t0002 | g0068 | EAS | JPT | MFSD8_chr4_127912805_127970173 | MFSD8 | chr4 | 127912805 | 127970173 |
| NA19074 | hp1 | a0001 | c0001 | t0001 | g0255 | EAS | JPT | MFSD8_chr4_127912805_127970173 | MFSD8 | chr4 | 127912805 | 127970173 |
| NA19074 | hp2 | a0003 | c0003 | t0001 | g0178 | EAS | JPT | MFSD8_chr4_127912805_127970173 | MFSD8 | chr4 | 127912805 | 127970173 |
| NA19075 | hp1 | a0002 | c0002 | t0002 | g0080 | EAS | JPT | MFSD8_chr4_127912805_127970173 | MFSD8 | chr4 | 127912805 | 127970173 |
| NA19075 | hp2 | a0001 | c0001 | t0008 | g0243 | EAS | JPT | MFSD8_chr4_127912805_127970173 | MFSD8 | chr4 | 127912805 | 127970173 |
| NA19077 | hp1 | a0001 | c0001 | t0001 | g0240 | EAS | JPT | MFSD8_chr4_127912805_127970173 | MFSD8 | chr4 | 127912805 | 127970173 |
| NA19077 | hp2 | a0002 | c0002 | t0002 | g0076 | EAS | JPT | MFSD8_chr4_127912805_127970173 | MFSD8 | chr4 | 127912805 | 127970173 |
| NA19078 | hp1 | a0002 | c0002 | t0013 | g0033 | EAS | JPT | MFSD8_chr4_127912805_127970173 | MFSD8 | chr4 | 127912805 | 127970173 |
| NA19078 | hp2 | a0001 | c0001 | t0001 | g0115 | EAS | JPT | MFSD8_chr4_127912805_127970173 | MFSD8 | chr4 | 127912805 | 127970173 |
| NA19083 | hp1 | a0002 | c0002 | t0002 | g0085 | EAS | JPT | MFSD8_chr4_127912805_127970173 | MFSD8 | chr4 | 127912805 | 127970173 |
| NA19083 | hp2 | a0002 | c0002 | t0002 | g0041 | EAS | JPT | MFSD8_chr4_127912805_127970173 | MFSD8 | chr4 | 127912805 | 127970173 |
| NA19085 | hp1 | a0001 | c0001 | t0001 | g0147 | EAS | JPT | MFSD8_chr4_127912805_127970173 | MFSD8 | chr4 | 127912805 | 127970173 |
| NA19085 | hp2 | a0002 | c0002 | t0002 | g0043 | EAS | JPT | MFSD8_chr4_127912805_127970173 | MFSD8 | chr4 | 127912805 | 127970173 |
| NA19090 | hp1 | a0008 | c0008 | t0001 | g0213 | EAS | JPT | MFSD8_chr4_127912805_127970173 | MFSD8 | chr4 | 127912805 | 127970173 |
| NA19090 | hp2 | a0002 | c0002 | t0002 | g0046 | EAS | JPT | MFSD8_chr4_127912805_127970173 | MFSD8 | chr4 | 127912805 | 127970173 |
| NA19091 | hp1 | a0001 | c0001 | t0001 | g0277 | EAS | JPT | MFSD8_chr4_127912805_127970173 | MFSD8 | chr4 | 127912805 | 127970173 |
| NA19091 | hp2 | a0002 | c0002 | t0002 | g0061 | EAS | JPT | MFSD8_chr4_127912805_127970173 | MFSD8 | chr4 | 127912805 | 127970173 |
| NA19240 | hp1 | a0001 | c0001 | t0020 | g0250 | AFR | YRI | MFSD8_chr4_127912805_127970173 | MFSD8 | chr4 | 127912805 | 127970173 |
| NA19240 | hp2 | a0001 | c0001 | t0001 | g0106 | AFR | YRI | MFSD8_chr4_127912805_127970173 | MFSD8 | chr4 | 127912805 | 127970173 |
| NA20129 | hp1 | a0001 | c0001 | t0016 | g0177 | AFR | ASW | MFSD8_chr4_127912805_127970173 | MFSD8 | chr4 | 127912805 | 127970173 |
| NA20129 | hp2 | a0001 | c0001 | t0001 | g0238 | AFR | ASW | MFSD8_chr4_127912805_127970173 | MFSD8 | chr4 | 127912805 | 127970173 |
| NA20752 | hp1 | a0001 | c0001 | t0001 | g0278 | EUR | TSI | MFSD8_chr4_127912805_127970173 | MFSD8 | chr4 | 127912805 | 127970173 |
| NA20752 | hp2 | a0001 | c0001 | t0001 | g0190 | EUR | TSI | MFSD8_chr4_127912805_127970173 | MFSD8 | chr4 | 127912805 | 127970173 |
| HG02109 | hp1 | a0002 | c0002 | t0003 | g0096 | AFR | ACB | MFSD8_chr4_127912805_127970173 | MFSD8 | chr4 | 127912805 | 127970173 |
| HG02109 | hp2 | a0001 | c0001 | t0001 | g0230 | AFR | ACB | MFSD8_chr4_127912805_127970173 | MFSD8 | chr4 | 127912805 | 127970173 |
| HG02486 | hp1 | a0002 | c0002 | t0012 | g0317 | AFR | ACB | MFSD8_chr4_127912805_127970173 | MFSD8 | chr4 | 127912805 | 127970173 |
| HG02486 | hp2 | a0002 | c0002 | t0006 | g0090 | AFR | ACB | MFSD8_chr4_127912805_127970173 | MFSD8 | chr4 | 127912805 | 127970173 |
| HG02559 | hp1 | a0001 | c0001 | t0001 | g0266 | AFR | ACB | MFSD8_chr4_127912805_127970173 | MFSD8 | chr4 | 127912805 | 127970173 |
| HG02559 | hp2 | a0001 | c0001 | t0001 | g0151 | AFR | ACB | MFSD8_chr4_127912805_127970173 | MFSD8 | chr4 | 127912805 | 127970173 |
| HG03471 | hp1 | a0001 | c0001 | t0001 | g0298 | AFR | MSL | MFSD8_chr4_127912805_127970173 | MFSD8 | chr4 | 127912805 | 127970173 |
| HG03471 | hp2 | a0006 | c0006 | t0001 | g0303 | AFR | MSL | MFSD8_chr4_127912805_127970173 | MFSD8 | chr4 | 127912805 | 127970173 |
| HG06807 | hp1 | a0001 | c0001 | t0001 | g0012 | AFR | USA | MFSD8_chr4_127912805_127970173 | MFSD8 | chr4 | 127912805 | 127970173 |
| HG06807 | hp2 | a0002 | c0002 | t0003 | g0099 | AFR | USA | MFSD8_chr4_127912805_127970173 | MFSD8 | chr4 | 127912805 | 127970173 |
| NA18955 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | MFSD8_chr4_127912805_127970173 | MFSD8 | chr4 | 127912805 | 127970173 |
| NA18955 | hp2 | a0002 | c0002 | t0004 | g0048 | EAS | JPT | MFSD8_chr4_127912805_127970173 | MFSD8 | chr4 | 127912805 | 127970173 |
| NA20300 | hp1 | a0001 | c0001 | t0001 | g0131 | AFR | USA | MFSD8_chr4_127912805_127970173 | MFSD8 | chr4 | 127912805 | 127970173 |
| NA20300 | hp2 | a0001 | c0001 | t0001 | g0122 | AFR | USA | MFSD8_chr4_127912805_127970173 | MFSD8 | chr4 | 127912805 | 127970173 |
| NA21309 | hp1 | a0001 | c0001 | t0001 | g0224 | AFR | LWK | MFSD8_chr4_127912805_127970173 | MFSD8 | chr4 | 127912805 | 127970173 |
| NA21309 | hp2 | a0001 | c0001 | t0001 | g0171 | AFR | LWK | MFSD8_chr4_127912805_127970173 | MFSD8 | chr4 | 127912805 | 127970173 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0001 | g0137 | REF | REF | MFSD8_chr4_127912805_127970173 | MFSD8 | chr4 | 127912805 | 127970173 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0001 | g0019 | REF | REF | MFSD8_chr4_127912805_127970173 | MFSD8 | chr4 | 127912805 | 127970173 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr4:127920671 | G | C | 1 | a0008 | 1 | NA19090.hp1 | missense_variant | MODERATE | c.1516C>G | p.Leu506Val | MFSD8 | ENSG00000164073.11 | transcript | ENST00000641686.2 | protein_coding | 12/12 | 1556/4422 | 1516/1557 | 506/518 | chr4 | 127920671 | |||
| chr4:127921606 | G | A | 3 | a0002 a0004 a0007 |
92 | HG00423.hp2 HG00438.hp2 HG00544.hp1 others(89): Show |
missense_variant | MODERATE | c.1268C>T | p.Ala423Val | MFSD8 | ENSG00000164073.11 | transcript | ENST00000641686.2 | protein_coding | 11/12 | 1308/4422 | 1268/1557 | 423/518 | chr4 | 127921606 | |||
| chr4:127921721 | C | G | 1 | a0003 | 16 | HG00408.hp1 HG00558.hp1 HG00609.hp1 others(13): Show |
missense_variant | MODERATE | c.1153G>C | p.Gly385Arg | MFSD8 | ENSG00000164073.11 | transcript | ENST00000641686.2 | protein_coding | 11/12 | 1193/4422 | 1153/1557 | 385/518 | chr4 | 127921721 | |||
| chr4:127930720 | C | T | 1 | a0005 | 1 | HG03453.hp1 | missense_variant | MODERATE | c.961G>A | p.Val321Ile | MFSD8 | ENSG00000164073.11 | transcript | ENST00000641686.2 | protein_coding | 9/12 | 1001/4422 | 961/1557 | 321/518 | chr4 | 127930720 | |||
| chr4:127939961 | C | T | 1 | a0006 | 1 | HG03471.hp2 | missense_variant | MODERATE | c.590G>A | p.Gly197Asp | MFSD8 | ENSG00000164073.11 | transcript | ENST00000641686.2 | protein_coding | 6/12 | 630/4422 | 590/1557 | 197/518 | chr4 | 127939961 | |||
| chr4:127943985 | G | A | 1 | a0007 | 1 | NA18986.hp1 | missense_variant | MODERATE | c.206C>T | p.Pro69Leu | MFSD8 | ENSG00000164073.11 | transcript | ENST00000641686.2 | protein_coding | 4/12 | 246/4422 | 206/1557 | 69/518 | chr4 | 127943985 | |||
| chr4:127957589 | T | A | 1 | a0004 | 3 | HG01496.hp1 HG02572.hp1 HG02922.hp2 |
missense_variant | MODERATE | c.66A>T | p.Glu22Asp | MFSD8 | ENSG00000164073.11 | transcript | ENST00000641686.2 | protein_coding | 2/12 | 106/4422 | 66/1557 | 22/518 | chr4 | 127957589 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr4:127921563 | G | C | 1 | a0001c0005 | 2 | HG02735.hp1 HG03017.hp2 |
synonymous_variant | LOW | c.1311C>G | p.Ser437Ser | MFSD8 | ENSG00000164073.11 | transcript | ENST00000641686.2 | protein_coding | 11/12 | 1351/4422 | 1311/1557 | 437/518 | chr4 | 127921563 | |||
| chr4:127921921 | T | C | 1 | a0001c0009 | 1 | HG02451.hp1 | synonymous_variant | LOW | c.1041A>G | p.Val347Val | MFSD8 | ENSG00000164073.11 | transcript | ENST00000641686.2 | protein_coding | 10/12 | 1081/4422 | 1041/1557 | 347/518 | chr4 | 127921921 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr4:127917941 | A | G | 1 | a0002c0002t0006 | 4 | HG01891.hp2 HG02486.hp2 HG02622.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*2689T>C | MFSD8 | ENSG00000164073.11 | transcript | ENST00000641686.2 | protein_coding | 12/12 | 2689 | chr4 | 127917941 | ||||||
| chr4:127918165 | T | C | 5 | a0002c0002t0002 a0002c0002t0004 a0002c0002t0013 others(2): Show |
70 | HG00423.hp2 HG00438.hp2 HG00544.hp1 others(67): Show |
3_prime_UTR_variant | MODIFIER | c.*2465A>G | MFSD8 | ENSG00000164073.11 | transcript | ENST00000641686.2 | protein_coding | 12/12 | 2465 | chr4 | 127918165 | ||||||
| chr4:127918166 | G | A | 2 | a0001c0001t0016 a0001c0001t0018 |
2 | HG03139.hp1 NA20129.hp1 |
3_prime_UTR_variant | MODIFIER | c.*2464C>T | MFSD8 | ENSG00000164073.11 | transcript | ENST00000641686.2 | protein_coding | 12/12 | 2464 | chr4 | 127918166 | ||||||
| chr4:127918200 | C | G | 1 | a0001c0001t0016 | 1 | NA20129.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2430G>C | MFSD8 | ENSG00000164073.11 | transcript | ENST00000641686.2 | protein_coding | 12/12 | 2430 | chr4 | 127918200 | ||||||
| chr4:127918223 | T | G | 1 | a0001c0001t0019 | 1 | HG02027.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2407A>C | MFSD8 | ENSG00000164073.11 | transcript | ENST00000641686.2 | protein_coding | 12/12 | 2407 | chr4 | 127918223 | ||||||
| chr4:127918225 | C | T | 1 | a0002c0002t0003 | 11 | HG02109.hp1 HG02257.hp2 HG02451.hp2 others(8): Show |
3_prime_UTR_variant | MODIFIER | c.*2405G>A | MFSD8 | ENSG00000164073.11 | transcript | ENST00000641686.2 | protein_coding | 12/12 | 2405 | chr4 | 127918225 | ||||||
| chr4:127918261 | G | C | 1 | a0001c0001t0008 | 3 | NA18949.hp2 NA19062.hp2 NA19075.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2369C>G | MFSD8 | ENSG00000164073.11 | transcript | ENST00000641686.2 | protein_coding | 12/12 | 2369 | chr4 | 127918261 | ||||||
| chr4:127918308 | T | C | 1 | a0001c0001t0011 | 2 | NA18987.hp2 NA18998.hp1 |
3_prime_UTR_variant | MODIFIER | c.*2322A>G | MFSD8 | ENSG00000164073.11 | transcript | ENST00000641686.2 | protein_coding | 12/12 | 2322 | chr4 | 127918308 | ||||||
| chr4:127918412 | G | A | 1 | a0001c0001t0020 | 1 | NA19240.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2218C>T | MFSD8 | ENSG00000164073.11 | transcript | ENST00000641686.2 | protein_coding | 12/12 | 2218 | chr4 | 127918412 | ||||||
| chr4:127918426 | GTTAAGT | G | 1 | a0002c0002t0004 | 5 | HG00558.hp2 HG00738.hp1 HG01358.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*2198_*2203delACTT others(2): Show |
MFSD8 | ENSG00000164073.11 | transcript | ENST00000641686.2 | protein_coding | 12/12 | 2198 | chr4 | 127918426 | ||||||
| chr4:127918476 | A | C | 1 | a0004c0004t0010 | 2 | HG01496.hp1 HG02922.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2154T>G | MFSD8 | ENSG00000164073.11 | transcript | ENST00000641686.2 | protein_coding | 12/12 | 2154 | chr4 | 127918476 | ||||||
| chr4:127918526 | A | G | 1 | a0001c0001t0017 | 1 | HG02083.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2104T>C | MFSD8 | ENSG00000164073.11 | transcript | ENST00000641686.2 | protein_coding | 12/12 | 2104 | chr4 | 127918526 | ||||||
| chr4:127918546 | T | G | 1 | a0003c0003t0021 | 1 | HG02056.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2084A>C | MFSD8 | ENSG00000164073.11 | transcript | ENST00000641686.2 | protein_coding | 12/12 | 2084 | chr4 | 127918546 | ||||||
| chr4:127918776 | A | T | 1 | a0001c0001t0016 | 1 | NA20129.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1854T>A | MFSD8 | ENSG00000164073.11 | transcript | ENST00000641686.2 | protein_coding | 12/12 | 1854 | chr4 | 127918776 | ||||||
| chr4:127918800 | A | G | 1 | a0001c0001t0015 | 1 | HG02717.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1830T>C | MFSD8 | ENSG00000164073.11 | transcript | ENST00000641686.2 | protein_coding | 12/12 | 1830 | chr4 | 127918800 | ||||||
| chr4:127918836 | C | A | 3 | a0002c0002t0005 a0004c0004t0005 a0004c0004t0010 |
6 | HG01496.hp1 HG02055.hp2 HG02572.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*1794G>T | MFSD8 | ENSG00000164073.11 | transcript | ENST00000641686.2 | protein_coding | 12/12 | 1794 | chr4 | 127918836 | ||||||
| chr4:127919115 | A | T | 1 | a0001c0001t0007 | 4 | NA18950.hp2 NA18973.hp2 NA18977.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*1515T>A | MFSD8 | ENSG00000164073.11 | transcript | ENST00000641686.2 | protein_coding | 12/12 | 1515 | chr4 | 127919115 | ||||||
| chr4:127919350 | A | T | 1 | a0001c0009t0014 | 1 | HG02451.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1280T>A | MFSD8 | ENSG00000164073.11 | transcript | ENST00000641686.2 | protein_coding | 12/12 | 1280 | chr4 | 127919350 | ||||||
| chr4:127919572 | T | C | 1 | a0002c0002t0013 | 1 | NA19078.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1058A>G | MFSD8 | ENSG00000164073.11 | transcript | ENST00000641686.2 | protein_coding | 12/12 | 1058 | chr4 | 127919572 | ||||||
| chr4:127919835 | G | GTA | 1 | a0002c0002t0006 | 4 | HG01891.hp2 HG02486.hp2 HG02622.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*793_*794dupTA | MFSD8 | ENSG00000164073.11 | transcript | ENST00000641686.2 | protein_coding | 12/12 | 794 | chr4 | 127919835 | ||||||
| chr4:127919955 | A | G | 1 | a0002c0002t0012 | 1 | HG02486.hp1 | 3_prime_UTR_variant | MODIFIER | c.*675T>C | MFSD8 | ENSG00000164073.11 | transcript | ENST00000641686.2 | protein_coding | 12/12 | 675 | chr4 | 127919955 | ||||||
| chr4:127920097 | C | T | 11 | a0002c0002t0002 a0002c0002t0003 a0002c0002t0004 others(8): Show |
92 | HG00423.hp2 HG00438.hp2 HG00544.hp1 others(89): Show |
3_prime_UTR_variant | MODIFIER | c.*533G>A | MFSD8 | ENSG00000164073.11 | transcript | ENST00000641686.2 | protein_coding | 12/12 | 533 | chr4 | 127920097 | ||||||
| chr4:127920111 | T | C | 1 | a0001c0001t0022 | 1 | HG02280.hp2 | 3_prime_UTR_variant | MODIFIER | c.*519A>G | MFSD8 | ENSG00000164073.11 | transcript | ENST00000641686.2 | protein_coding | 12/12 | 519 | chr4 | 127920111 | ||||||
| chr4:127920167 | T | A | 1 | a0002c0002t0023 | 1 | NA19005.hp1 | 3_prime_UTR_variant | MODIFIER | c.*463A>T | MFSD8 | ENSG00000164073.11 | transcript | ENST00000641686.2 | protein_coding | 12/12 | 463 | chr4 | 127920167 | ||||||
| chr4:127920203 | C | G | 1 | a0003c0003t0009 | 2 | HG01943.hp2 HG01952.hp2 |
3_prime_UTR_variant | MODIFIER | c.*427G>C | MFSD8 | ENSG00000164073.11 | transcript | ENST00000641686.2 | protein_coding | 12/12 | 427 | chr4 | 127920203 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr4:127920845 | G | A | 3 | a0002c0002t0005g0312 a0002c0002t0005g0313 a0002c0002t0005g0314 |
3 | HG02055.hp2 HG02976.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.1351-9C>T | MFSD8 | ENSG00000164073.11 | transcript | ENST00000641686.2 | protein_coding | 11/11 | chr4 | 127920845 | |||||||
| chr4:127920919 | C | G | 11 | a0002c0002t0003g0093 a0002c0002t0003g0094 a0002c0002t0003g0095 others(8): Show |
11 | HG02109.hp1 HG02257.hp2 HG02451.hp2 others(8): Show |
intron_variant | MODIFIER | c.1351-83G>C | MFSD8 | ENSG00000164073.11 | transcript | ENST00000641686.2 | protein_coding | 11/11 | chr4 | 127920919 | |||||||
| chr4:127921182 | G | C | 1 | a0001c0001t0001g0227 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.1350+342C>G | MFSD8 | ENSG00000164073.11 | transcript | ENST00000641686.2 | protein_coding | 11/11 | chr4 | 127921182 | |||||||
| chr4:127921414 | G | T | 1 | a0001c0001t0001g0304 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.1350+110C>A | MFSD8 | ENSG00000164073.11 | transcript | ENST00000641686.2 | protein_coding | 11/11 | chr4 | 127921414 | |||||||
| chr4:127922114 | T | A | 1 | a0001c0001t0001g0271 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.999-151A>T | MFSD8 | ENSG00000164073.11 | transcript | ENST00000641686.2 | protein_coding | 9/11 | chr4 | 127922114 | |||||||
| chr4:127922183 | T | C | 2 | a0001c0001t0001g0260 a0001c0001t0001g0267 |
2 | HG02572.hp2 HG02723.hp2 |
intron_variant | MODIFIER | c.999-220A>G | MFSD8 | ENSG00000164073.11 | transcript | ENST00000641686.2 | protein_coding | 9/11 | chr4 | 127922183 | |||||||
| chr4:127922325 | A | G | 19 | a0001c0001t0001g0017 a0001c0001t0001g0024 a0001c0001t0001g0115 others(16): Show |
20 | HG00140.hp2 HG01884.hp2 HG02015.hp2 others(17): Show |
intron_variant | MODIFIER | c.999-362T>C | MFSD8 | ENSG00000164073.11 | transcript | ENST00000641686.2 | protein_coding | 9/11 | chr4 | 127922325 | |||||||
| chr4:127922449 | C | A | 1 | a0001c0001t0001g0288 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.999-486G>T | MFSD8 | ENSG00000164073.11 | transcript | ENST00000641686.2 | protein_coding | 9/11 | chr4 | 127922449 | |||||||
| chr4:127922482 | A | G | 11 | a0002c0002t0003g0093 a0002c0002t0003g0094 a0002c0002t0003g0095 others(8): Show |
11 | HG02109.hp1 HG02257.hp2 HG02451.hp2 others(8): Show |
intron_variant | MODIFIER | c.999-519T>C | MFSD8 | ENSG00000164073.11 | transcript | ENST00000641686.2 | protein_coding | 9/11 | chr4 | 127922482 | |||||||
| chr4:127922620 | G | A | 11 | a0002c0002t0003g0093 a0002c0002t0003g0094 a0002c0002t0003g0095 others(8): Show |
11 | HG02109.hp1 HG02257.hp2 HG02451.hp2 others(8): Show |
intron_variant | MODIFIER | c.999-657C>T | MFSD8 | ENSG00000164073.11 | transcript | ENST00000641686.2 | protein_coding | 9/11 | chr4 | 127922620 | |||||||
| chr4:127922660 | T | C | 1 | a0002c0002t0012g0317 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.999-697A>G | MFSD8 | ENSG00000164073.11 | transcript | ENST00000641686.2 | protein_coding | 9/11 | chr4 | 127922660 | |||||||
| chr4:127922891 | A | G | 11 | a0002c0002t0003g0093 a0002c0002t0003g0094 a0002c0002t0003g0095 others(8): Show |
11 | HG02109.hp1 HG02257.hp2 HG02451.hp2 others(8): Show |
intron_variant | MODIFIER | c.999-928T>C | MFSD8 | ENSG00000164073.11 | transcript | ENST00000641686.2 | protein_coding | 9/11 | chr4 | 127922891 | |||||||
| chr4:127923297 | G | A | 11 | a0002c0002t0003g0093 a0002c0002t0003g0094 a0002c0002t0003g0095 others(8): Show |
11 | HG02109.hp1 HG02257.hp2 HG02451.hp2 others(8): Show |
intron_variant | MODIFIER | c.999-1334C>T | MFSD8 | ENSG00000164073.11 | transcript | ENST00000641686.2 | protein_coding | 9/11 | chr4 | 127923297 | |||||||
| chr4:127923374 | A | T | 1 | a0002c0002t0012g0317 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.999-1411T>A | MFSD8 | ENSG00000164073.11 | transcript | ENST00000641686.2 | protein_coding | 9/11 | chr4 | 127923374 | |||||||
| chr4:127923512 | T | C | 11 | a0002c0002t0003g0093 a0002c0002t0003g0094 a0002c0002t0003g0095 others(8): Show |
11 | HG02109.hp1 HG02257.hp2 HG02451.hp2 others(8): Show |
intron_variant | MODIFIER | c.999-1549A>G | MFSD8 | ENSG00000164073.11 | transcript | ENST00000641686.2 | protein_coding | 9/11 | chr4 | 127923512 | |||||||
| chr4:127923541 | T | A | 1 | a0001c0001t0001g0201 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.999-1578A>T | MFSD8 | ENSG00000164073.11 | transcript | ENST00000641686.2 | protein_coding | 9/11 | chr4 | 127923541 | |||||||
| chr4:127923545 | A | T | 1 | a0001c0001t0001g0201 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.999-1582T>A | MFSD8 | ENSG00000164073.11 | transcript | ENST00000641686.2 | protein_coding | 9/11 | chr4 | 127923545 | |||||||
| chr4:127923547 | T | A | 2 | a0001c0001t0001g0201 a0002c0002t0012g0317 |
2 | HG00544.hp2 HG02486.hp1 |
intron_variant | MODIFIER | c.999-1584A>T | MFSD8 | ENSG00000164073.11 | transcript | ENST00000641686.2 | protein_coding | 9/11 | chr4 | 127923547 | |||||||
| chr4:127923547 | T | TTTTA | 6 | a0001c0001t0001g0022 a0001c0001t0001g0260 a0001c0001t0001g0308 others(3): Show |
7 | HG01168.hp2 HG02055.hp2 HG02451.hp1 others(4): Show |
intron_variant | MODIFIER | c.999-1588_999-1585d others(6): Show |
MFSD8 | ENSG00000164073.11 | transcript | ENST00000641686.2 | protein_coding | 9/11 | chr4 | 127923547 | |||||||
| chr4:127923552 | T | TTTA | 80 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0005 others(77): Show |
89 | HG00099.hp2 HG00140.hp1 HG00423.hp1 others(86): Show |
intron_variant | MODIFIER | c.999-1592_999-1590d others(5): Show |
MFSD8 | ENSG00000164073.11 | transcript | ENST00000641686.2 | protein_coding | 9/11 | chr4 | 127923552 | |||||||
| chr4:127923552 | T | TTTATTA | 38 | a0001c0001t0001g0002 a0001c0001t0001g0014 a0001c0001t0001g0018 others(35): Show |
43 | HG00408.hp2 HG00597.hp1 HG00741.hp2 others(40): Show |
intron_variant | MODIFIER | c.999-1595_999-1590d others(8): Show |
MFSD8 | ENSG00000164073.11 | transcript | ENST00000641686.2 | protein_coding | 9/11 | chr4 | 127923552 | |||||||
| chr4:127923552 | T | TTTATTAT others(2): Show |
12 | a0001c0001t0001g0002 a0001c0001t0001g0018 a0001c0001t0001g0151 others(9): Show |
12 | HG02165.hp2 HG02257.hp2 HG02559.hp1 others(9): Show |
intron_variant | MODIFIER | c.999-1598_999-1590d others(11): Show |
MFSD8 | ENSG00000164073.11 | transcript | ENST00000641686.2 | protein_coding | 9/11 | chr4 | 127923552 | |||||||
| chr4:127923552 | T | TTTATTAT others(5): Show |
2 | a0001c0001t0001g0248 a0001c0001t0001g0263 |
2 | HG03834.hp1 NA19009.hp2 |
intron_variant | MODIFIER | c.999-1601_999-1590d others(14): Show |
MFSD8 | ENSG00000164073.11 | transcript | ENST00000641686.2 | protein_coding | 9/11 | chr4 | 127923552 | |||||||
| chr4:127923552 | T | TTTATTTA | 6 | a0001c0001t0001g0107 a0001c0001t0001g0131 a0001c0001t0001g0267 others(3): Show |
6 | HG02280.hp2 HG02572.hp2 HG02970.hp1 others(3): Show |
intron_variant | MODIFIER | c.999-1590_999-1589i others(9): Show |
MFSD8 | ENSG00000164073.11 | transcript | ENST00000641686.2 | protein_coding | 9/11 | chr4 | 127923552 | |||||||
| chr4:127923552 | T | TTTATTTA others(3): Show |
1 | a0001c0001t0001g0106 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.999-1590_999-1589i others(12): Show |
MFSD8 | ENSG00000164073.11 | transcript | ENST00000641686.2 | protein_coding | 9/11 | chr4 | 127923552 | |||||||
| chr4:127923552 | TTTA | T | 95 | a0001c0001t0001g0015 a0001c0001t0001g0017 a0001c0001t0001g0023 others(92): Show |
103 | HG00099.hp1 HG00140.hp2 HG00423.hp2 others(100): Show |
intron_variant | MODIFIER | c.999-1592_999-1590d others(5): Show |
MFSD8 | ENSG00000164073.11 | transcript | ENST00000641686.2 | protein_coding | 9/11 | chr4 | 127923552 | |||||||
| chr4:127923552 | TTTATTA | T | 8 | a0001c0001t0001g0235 a0001c0001t0001g0283 a0002c0002t0002g0054 others(5): Show |
8 | HG00408.hp1 HG00558.hp2 HG00621.hp2 others(5): Show |
intron_variant | MODIFIER | c.999-1595_999-1590d others(8): Show |
MFSD8 | ENSG00000164073.11 | transcript | ENST00000641686.2 | protein_coding | 9/11 | chr4 | 127923552 | |||||||
| chr4:127923555 | A | AT | 6 | a0001c0001t0001g0012 a0001c0001t0001g0114 a0001c0001t0001g0116 others(3): Show |
7 | HG00741.hp1 HG02647.hp1 HG02886.hp2 others(4): Show |
intron_variant | MODIFIER | c.999-1593dupA | MFSD8 | ENSG00000164073.11 | transcript | ENST00000641686.2 | protein_coding | 9/11 | chr4 | 127923555 | |||||||
| chr4:127923555 | A | ATTTAT | 3 | a0002c0002t0006g0089 a0002c0002t0006g0090 a0002c0002t0006g0306 |
3 | HG02486.hp2 HG02622.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.999-1593_999-1592i others(7): Show |
MFSD8 | ENSG00000164073.11 | transcript | ENST00000641686.2 | protein_coding | 9/11 | chr4 | 127923555 | |||||||
| chr4:127923556 | TTA | T | 5 | a0001c0001t0001g0108 a0001c0001t0001g0110 a0001c0001t0001g0111 others(2): Show |
5 | HG02258.hp2 HG02717.hp2 HG02965.hp2 others(2): Show |
intron_variant | MODIFIER | c.999-1595_999-1594d others(4): Show |
MFSD8 | ENSG00000164073.11 | transcript | ENST00000641686.2 | protein_coding | 9/11 | chr4 | 127923556 | |||||||
| chr4:127923556 | TTATTA | T | 2 | a0004c0004t0005g0092 a0004c0004t0010g0011 |
3 | HG01496.hp1 HG02572.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.999-1598_999-1594d others(7): Show |
MFSD8 | ENSG00000164073.11 | transcript | ENST00000641686.2 | protein_coding | 9/11 | chr4 | 127923556 | |||||||
| chr4:127923558 | A | T | 1 | a0002c0002t0006g0091 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.999-1595T>A | MFSD8 | ENSG00000164073.11 | transcript | ENST00000641686.2 | protein_coding | 9/11 | chr4 | 127923558 | |||||||
| chr4:127923610 | T | C | 311 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(308): Show |
346 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(343): Show |
intron_variant | MODIFIER | c.999-1647A>G | MFSD8 | ENSG00000164073.11 | transcript | ENST00000641686.2 | protein_coding | 9/11 | chr4 | 127923610 | |||||||
| chr4:127923665 | C | T | 3 | a0001c0001t0001g0207 a0001c0001t0001g0208 a0002c0002t0012g0317 |
3 | HG01257.hp2 HG01258.hp2 HG02486.hp1 |
intron_variant | MODIFIER | c.999-1702G>A | MFSD8 | ENSG00000164073.11 | transcript | ENST00000641686.2 | protein_coding | 9/11 | chr4 | 127923665 | |||||||
| chr4:127923807 | T | TC | 80 | a0002c0002t0002g0004 a0002c0002t0002g0008 a0002c0002t0002g0009 others(77): Show |
86 | HG00423.hp2 HG00438.hp2 HG00544.hp1 others(83): Show |
intron_variant | MODIFIER | c.999-1845dupG | MFSD8 | ENSG00000164073.11 | transcript | ENST00000641686.2 | protein_coding | 9/11 | chr4 | 127923807 | |||||||
| chr4:127923890 | A | C | 11 | a0002c0002t0003g0093 a0002c0002t0003g0094 a0002c0002t0003g0095 others(8): Show |
11 | HG02109.hp1 HG02257.hp2 HG02451.hp2 others(8): Show |
intron_variant | MODIFIER | c.999-1927T>G | MFSD8 | ENSG00000164073.11 | transcript | ENST00000641686.2 | protein_coding | 9/11 | chr4 | 127923890 | |||||||
| chr4:127923910 | C | T | 18 | a0001c0001t0001g0023 a0001c0001t0001g0222 a0001c0001t0001g0223 others(15): Show |
18 | HG00735.hp1 HG02109.hp2 HG02258.hp1 others(15): Show |
intron_variant | MODIFIER | c.999-1947G>A | MFSD8 | ENSG00000164073.11 | transcript | ENST00000641686.2 | protein_coding | 9/11 | chr4 | 127923910 | |||||||
| chr4:127923951 | T | G | 1 | a0001c0001t0001g0114 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.999-1988A>C | MFSD8 | ENSG00000164073.11 | transcript | ENST00000641686.2 | protein_coding | 9/11 | chr4 | 127923951 | |||||||
| chr4:127923987 | T | G | 11 | a0002c0002t0003g0093 a0002c0002t0003g0094 a0002c0002t0003g0095 others(8): Show |
11 | HG02109.hp1 HG02257.hp2 HG02451.hp2 others(8): Show |
intron_variant | MODIFIER | c.999-2024A>C | MFSD8 | ENSG00000164073.11 | transcript | ENST00000641686.2 | protein_coding | 9/11 | chr4 | 127923987 | |||||||
| chr4:127924057 | G | A | 4 | a0002c0002t0006g0089 a0002c0002t0006g0090 a0002c0002t0006g0091 others(1): Show |
4 | HG01891.hp2 HG02486.hp2 HG02622.hp2 others(1): Show |
intron_variant | MODIFIER | c.999-2094C>T | MFSD8 | ENSG00000164073.11 | transcript | ENST00000641686.2 | protein_coding | 9/11 | chr4 | 127924057 | |||||||
| chr4:127924091 | A | G | 85 | a0002c0002t0002g0004 a0002c0002t0002g0008 a0002c0002t0002g0009 others(82): Show |
92 | HG00423.hp2 HG00438.hp2 HG00544.hp1 others(89): Show |
intron_variant | MODIFIER | c.999-2128T>C | MFSD8 | ENSG00000164073.11 | transcript | ENST00000641686.2 | protein_coding | 9/11 | chr4 | 127924091 | |||||||
| chr4:127924322 | C | A | 1 | a0002c0002t0012g0317 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.999-2359G>T | MFSD8 | ENSG00000164073.11 | transcript | ENST00000641686.2 | protein_coding | 9/11 | chr4 | 127924322 | |||||||
| chr4:127924475 | G | T | 2 | a0001c0001t0001g0264 a0001c0001t0001g0269 |
2 | HG00099.hp2 HG01175.hp2 |
intron_variant | MODIFIER | c.999-2512C>A | MFSD8 | ENSG00000164073.11 | transcript | ENST00000641686.2 | protein_coding | 9/11 | chr4 | 127924475 | |||||||
| chr4:127924822 | C | T | 1 | a0001c0001t0001g0109 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.999-2859G>A | MFSD8 | ENSG00000164073.11 | transcript | ENST00000641686.2 | protein_coding | 9/11 | chr4 | 127924822 | |||||||
| chr4:127925205 | C | G | 1 | a0004c0004t0010g0011 | 2 | HG01496.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.999-3242G>C | MFSD8 | ENSG00000164073.11 | transcript | ENST00000641686.2 | protein_coding | 9/11 | chr4 | 127925205 | |||||||
| chr4:127925433 | T | C | 1 | a0001c0001t0001g0149 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.999-3470A>G | MFSD8 | ENSG00000164073.11 | transcript | ENST00000641686.2 | protein_coding | 9/11 | chr4 | 127925433 | |||||||
| chr4:127925437 | C | G | 1 | a0001c0001t0001g0020 | 2 | NA18954.hp1 NA18957.hp1 |
intron_variant | MODIFIER | c.999-3474G>C | MFSD8 | ENSG00000164073.11 | transcript | ENST00000641686.2 | protein_coding | 9/11 | chr4 | 127925437 | |||||||
| chr4:127925504 | G | C | 11 | a0002c0002t0003g0093 a0002c0002t0003g0094 a0002c0002t0003g0095 others(8): Show |
11 | HG02109.hp1 HG02257.hp2 HG02451.hp2 others(8): Show |
intron_variant | MODIFIER | c.999-3541C>G | MFSD8 | ENSG00000164073.11 | transcript | ENST00000641686.2 | protein_coding | 9/11 | chr4 | 127925504 | |||||||
| chr4:127925581 | G | A | 2 | a0004c0004t0005g0092 a0004c0004t0010g0011 |
3 | HG01496.hp1 HG02572.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.999-3618C>T | MFSD8 | ENSG00000164073.11 | transcript | ENST00000641686.2 | protein_coding | 9/11 | chr4 | 127925581 | |||||||
| chr4:127925697 | T | G | 5 | a0002c0002t0005g0312 a0002c0002t0005g0313 a0002c0002t0005g0314 others(2): Show |
6 | HG01496.hp1 HG02055.hp2 HG02572.hp1 others(3): Show |
intron_variant | MODIFIER | c.999-3734A>C | MFSD8 | ENSG00000164073.11 | transcript | ENST00000641686.2 | protein_coding | 9/11 | chr4 | 127925697 | |||||||
| chr4:127925747 | C | T | 1 | a0001c0001t0001g0270 | 1 | NA19065.hp2 | intron_variant | MODIFIER | c.999-3784G>A | MFSD8 | ENSG00000164073.11 | transcript | ENST00000641686.2 | protein_coding | 9/11 | chr4 | 127925747 | |||||||
| chr4:127925845 | C | T | 1 | a0001c0001t0001g0315 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.999-3882G>A | MFSD8 | ENSG00000164073.11 | transcript | ENST00000641686.2 | protein_coding | 9/11 | chr4 | 127925845 | |||||||
| chr4:127925869 | G | T | 1 | a0001c0001t0001g0182 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.999-3906C>A | MFSD8 | ENSG00000164073.11 | transcript | ENST00000641686.2 | protein_coding | 9/11 | chr4 | 127925869 | |||||||
| chr4:127925971 | C | T | 7 | a0001c0001t0001g0136 a0001c0001t0001g0156 a0001c0001t0001g0161 others(4): Show |
7 | HG00140.hp2 HG02735.hp1 HG03017.hp2 others(4): Show |
intron_variant | MODIFIER | c.999-4008G>A | MFSD8 | ENSG00000164073.11 | transcript | ENST00000641686.2 | protein_coding | 9/11 | chr4 | 127925971 | |||||||
| chr4:127925995 | A | C | 4 | a0002c0002t0002g0036 a0002c0002t0002g0041 a0002c0002t0002g0042 others(1): Show |
4 | NA18970.hp1 NA18994.hp2 NA19062.hp1 others(1): Show |
intron_variant | MODIFIER | c.999-4032T>G | MFSD8 | ENSG00000164073.11 | transcript | ENST00000641686.2 | protein_coding | 9/11 | chr4 | 127925995 | |||||||
| chr4:127926024 | G | T | 1 | a0001c0001t0022g0309 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.999-4061C>A | MFSD8 | ENSG00000164073.11 | transcript | ENST00000641686.2 | protein_coding | 9/11 | chr4 | 127926024 | |||||||
| chr4:127926085 | C | T | 11 | a0002c0002t0003g0093 a0002c0002t0003g0094 a0002c0002t0003g0095 others(8): Show |
11 | HG02109.hp1 HG02257.hp2 HG02451.hp2 others(8): Show |
intron_variant | MODIFIER | c.999-4122G>A | MFSD8 | ENSG00000164073.11 | transcript | ENST00000641686.2 | protein_coding | 9/11 | chr4 | 127926085 | |||||||
| chr4:127926141 | G | A | 2 | a0002c0002t0002g0040 a0002c0002t0002g0043 |
2 | NA18984.hp1 NA19085.hp2 |
intron_variant | MODIFIER | c.999-4178C>T | MFSD8 | ENSG00000164073.11 | transcript | ENST00000641686.2 | protein_coding | 9/11 | chr4 | 127926141 | |||||||
| chr4:127926196 | G | C | 2 | a0004c0004t0005g0092 a0004c0004t0010g0011 |
3 | HG01496.hp1 HG02572.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.999-4233C>G | MFSD8 | ENSG00000164073.11 | transcript | ENST00000641686.2 | protein_coding | 9/11 | chr4 | 127926196 | |||||||
| chr4:127926315 | A | ATCCAGGC others(1004): Show |
11 | a0002c0002t0003g0093 a0002c0002t0003g0094 a0002c0002t0003g0095 others(8): Show |
11 | HG02109.hp1 HG02257.hp2 HG02451.hp2 others(8): Show |
intron_variant | MODIFIER | c.999-4353_999-4352i others(1013): Show |
MFSD8 | ENSG00000164073.11 | transcript | ENST00000641686.2 | protein_coding | 9/11 | chr4 | 127926315 | |||||||
| chr4:127926315 | A | ATCCAGGC others(1006): Show |
1 | a0001c0001t0001g0161 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.999-4353_999-4352i others(1015): Show |
MFSD8 | ENSG00000164073.11 | transcript | ENST00000641686.2 | protein_coding | 9/11 | chr4 | 127926315 | |||||||
| chr4:127926315 | A | ATCCAGGC others(1005): Show |
5 | a0001c0001t0001g0022 a0001c0001t0001g0307 a0001c0001t0001g0308 others(2): Show |
6 | HG01168.hp2 HG02280.hp2 HG02451.hp1 others(3): Show |
intron_variant | MODIFIER | c.999-4353_999-4352i others(1014): Show |
MFSD8 | ENSG00000164073.11 | transcript | ENST00000641686.2 | protein_coding | 9/11 | chr4 | 127926315 | |||||||
| chr4:127926315 | A | ATCCAGGC others(1004): Show |
1 | a0002c0002t0012g0317 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.999-4353_999-4352i others(1013): Show |
MFSD8 | ENSG00000164073.11 | transcript | ENST00000641686.2 | protein_coding | 9/11 | chr4 | 127926315 | |||||||
| chr4:127926315 | A | ATCCAGGC others(1006): Show |
5 | a0001c0001t0001g0142 a0001c0005t0001g0104 a0002c0002t0005g0312 others(2): Show |
5 | HG02055.hp2 HG02602.hp2 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.999-4353_999-4352i others(1015): Show |
MFSD8 | ENSG00000164073.11 | transcript | ENST00000641686.2 | protein_coding | 9/11 | chr4 | 127926315 | |||||||
| chr4:127926315 | A | ATCCAGGC others(1005): Show |
110 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(107): Show |
125 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(122): Show |
intron_variant | MODIFIER | c.999-4353_999-4352i others(1014): Show |
MFSD8 | ENSG00000164073.11 | transcript | ENST00000641686.2 | protein_coding | 9/11 | chr4 | 127926315 | |||||||
| chr4:127926315 | A | ATCCAGGC others(1005): Show |
2 | a0001c0001t0001g0135 a0001c0001t0001g0160 |
2 | HG00140.hp1 HG04228.hp2 |
intron_variant | MODIFIER | c.999-4353_999-4352i others(1014): Show |
MFSD8 | ENSG00000164073.11 | transcript | ENST00000641686.2 | protein_coding | 9/11 | chr4 | 127926315 | |||||||
| chr4:127926315 | A | ATCCAGGC others(1004): Show |
63 | a0001c0001t0001g0116 a0002c0002t0002g0004 a0002c0002t0002g0008 others(60): Show |
69 | HG00423.hp2 HG00438.hp2 HG00544.hp1 others(66): Show |
intron_variant | MODIFIER | c.999-4353_999-4352i others(1013): Show |
MFSD8 | ENSG00000164073.11 | transcript | ENST00000641686.2 | protein_coding | 9/11 | chr4 | 127926315 | |||||||
| chr4:127926315 | A | ATCCAGGC others(996): Show |
3 | a0002c0002t0002g0062 a0002c0002t0002g0065 a0002c0002t0002g0080 |
3 | HG02523.hp2 NA18947.hp1 NA19075.hp1 |
intron_variant | MODIFIER | c.999-4353_999-4352i others(1005): Show |
MFSD8 | ENSG00000164073.11 | transcript | ENST00000641686.2 | protein_coding | 9/11 | chr4 | 127926315 | |||||||
| chr4:127926315 | A | ATCCAGGC others(1003): Show |
4 | a0002c0002t0006g0089 a0002c0002t0006g0090 a0002c0002t0006g0091 others(1): Show |
4 | HG01891.hp2 HG02486.hp2 HG02622.hp2 others(1): Show |
intron_variant | MODIFIER | c.999-4353_999-4352i others(1012): Show |
MFSD8 | ENSG00000164073.11 | transcript | ENST00000641686.2 | protein_coding | 9/11 | chr4 | 127926315 | |||||||
| chr4:127926315 | A | ATCCAGGC others(1001): Show |
2 | a0004c0004t0005g0092 a0004c0004t0010g0011 |
3 | HG01496.hp1 HG02572.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.999-4353_999-4352i others(1010): Show |
MFSD8 | ENSG00000164073.11 | transcript | ENST00000641686.2 | protein_coding | 9/11 | chr4 | 127926315 | |||||||
| chr4:127926373 | T | TTCC | 65 | a0002c0002t0002g0004 a0002c0002t0002g0008 a0002c0002t0002g0009 others(62): Show |
71 | HG00423.hp2 HG00438.hp2 HG00544.hp1 others(68): Show |
intron_variant | MODIFIER | c.998+4307_998+4309d others(5): Show |
MFSD8 | ENSG00000164073.11 | transcript | ENST00000641686.2 | protein_coding | 9/11 | chr4 | 127926373 | |||||||
| chr4:127926388 | T | C | 11 | a0002c0002t0003g0093 a0002c0002t0003g0094 a0002c0002t0003g0095 others(8): Show |
11 | HG02109.hp1 HG02257.hp2 HG02451.hp2 others(8): Show |
intron_variant | MODIFIER | c.998+4295A>G | MFSD8 | ENSG00000164073.11 | transcript | ENST00000641686.2 | protein_coding | 9/11 | chr4 | 127926388 | |||||||
| chr4:127926737 | C | G | 1 | a0002c0002t0012g0317 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.998+3946G>C | MFSD8 | ENSG00000164073.11 | transcript | ENST00000641686.2 | protein_coding | 9/11 | chr4 | 127926737 | |||||||
| chr4:127926806 | C | T | 4 | a0002c0002t0006g0089 a0002c0002t0006g0090 a0002c0002t0006g0091 others(1): Show |
4 | HG01891.hp2 HG02486.hp2 HG02622.hp2 others(1): Show |
intron_variant | MODIFIER | c.998+3877G>A | MFSD8 | ENSG00000164073.11 | transcript | ENST00000641686.2 | protein_coding | 9/11 | chr4 | 127926806 | |||||||
| chr4:127927174 | GT | G | 196 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(193): Show |
219 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(216): Show |
intron_variant | MODIFIER | c.998+3508delA | MFSD8 | ENSG00000164073.11 | transcript | ENST00000641686.2 | protein_coding | 9/11 | chr4 | 127927174 | |||||||
| chr4:127927174 | GTT | G | 11 | a0002c0002t0003g0093 a0002c0002t0003g0094 a0002c0002t0003g0095 others(8): Show |
11 | HG02109.hp1 HG02257.hp2 HG02451.hp2 others(8): Show |
intron_variant | MODIFIER | c.998+3507_998+3508d others(4): Show |
MFSD8 | ENSG00000164073.11 | transcript | ENST00000641686.2 | protein_coding | 9/11 | chr4 | 127927174 | |||||||
| chr4:127927185 | T | G | 1 | a0001c0001t0001g0012 | 2 | HG02647.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.998+3498A>C | MFSD8 | ENSG00000164073.11 | transcript | ENST00000641686.2 | protein_coding | 9/11 | chr4 | 127927185 | |||||||
| chr4:127927194 | C | A | 1 | a0002c0002t0006g0089 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.998+3489G>T | MFSD8 | ENSG00000164073.11 | transcript | ENST00000641686.2 | protein_coding | 9/11 | chr4 | 127927194 | |||||||
| chr4:127927361 | C | T | 1 | a0001c0005t0001g0103 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.998+3322G>A | MFSD8 | ENSG00000164073.11 | transcript | ENST00000641686.2 | protein_coding | 9/11 | chr4 | 127927361 | |||||||
| chr4:127927422 | C | A | 1 | a0001c0001t0001g0015 | 2 | HG01515.hp2 HG01517.hp2 |
intron_variant | MODIFIER | c.998+3261G>T | MFSD8 | ENSG00000164073.11 | transcript | ENST00000641686.2 | protein_coding | 9/11 | chr4 | 127927422 | |||||||
| chr4:127927427 | T | C | 16 | a0002c0002t0003g0093 a0002c0002t0003g0094 a0002c0002t0003g0095 others(13): Show |
16 | HG01891.hp2 HG02109.hp1 HG02257.hp2 others(13): Show |
intron_variant | MODIFIER | c.998+3256A>G | MFSD8 | ENSG00000164073.11 | transcript | ENST00000641686.2 | protein_coding | 9/11 | chr4 | 127927427 | |||||||
| chr4:127927521 | A | C | 2 | a0004c0004t0005g0092 a0004c0004t0010g0011 |
3 | HG01496.hp1 HG02572.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.998+3162T>G | MFSD8 | ENSG00000164073.11 | transcript | ENST00000641686.2 | protein_coding | 9/11 | chr4 | 127927521 | |||||||
| chr4:127927630 | A | T | 1 | a0003c0003t0001g0165 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.998+3053T>A | MFSD8 | ENSG00000164073.11 | transcript | ENST00000641686.2 | protein_coding | 9/11 | chr4 | 127927630 | |||||||
| chr4:127927805 | A | G | 1 | a0003c0003t0021g0154 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.998+2878T>C | MFSD8 | ENSG00000164073.11 | transcript | ENST00000641686.2 | protein_coding | 9/11 | chr4 | 127927805 | |||||||
| chr4:127927908 | G | A | 1 | a0001c0001t0001g0288 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.998+2775C>T | MFSD8 | ENSG00000164073.11 | transcript | ENST00000641686.2 | protein_coding | 9/11 | chr4 | 127927908 | |||||||
| chr4:127927968 | C | G | 1 | a0001c0001t0001g0152 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.998+2715G>C | MFSD8 | ENSG00000164073.11 | transcript | ENST00000641686.2 | protein_coding | 9/11 | chr4 | 127927968 | |||||||
| chr4:127928078 | T | G | 1 | a0001c0001t0001g0209 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.998+2605A>C | MFSD8 | ENSG00000164073.11 | transcript | ENST00000641686.2 | protein_coding | 9/11 | chr4 | 127928078 | |||||||
| chr4:127928267 | T | C | 11 | a0002c0002t0003g0093 a0002c0002t0003g0094 a0002c0002t0003g0095 others(8): Show |
11 | HG02109.hp1 HG02257.hp2 HG02451.hp2 others(8): Show |
intron_variant | MODIFIER | c.998+2416A>G | MFSD8 | ENSG00000164073.11 | transcript | ENST00000641686.2 | protein_coding | 9/11 | chr4 | 127928267 | |||||||
| chr4:127928280 | G | T | 1 | a0001c0001t0001g0118 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.998+2403C>A | MFSD8 | ENSG00000164073.11 | transcript | ENST00000641686.2 | protein_coding | 9/11 | chr4 | 127928280 | |||||||
| chr4:127928427 | G | T | 1 | a0001c0009t0014g0310 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.998+2256C>A | MFSD8 | ENSG00000164073.11 | transcript | ENST00000641686.2 | protein_coding | 9/11 | chr4 | 127928427 | |||||||
| chr4:127928742 | T | C | 1 | a0001c0001t0001g0203 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.998+1941A>G | MFSD8 | ENSG00000164073.11 | transcript | ENST00000641686.2 | protein_coding | 9/11 | chr4 | 127928742 | |||||||
| chr4:127928885 | G | A | 2 | a0004c0004t0005g0092 a0004c0004t0010g0011 |
3 | HG01496.hp1 HG02572.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.998+1798C>T | MFSD8 | ENSG00000164073.11 | transcript | ENST00000641686.2 | protein_coding | 9/11 | chr4 | 127928885 | |||||||
| chr4:127928918 | G | C | 207 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(204): Show |
230 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(227): Show |
intron_variant | MODIFIER | c.998+1765C>G | MFSD8 | ENSG00000164073.11 | transcript | ENST00000641686.2 | protein_coding | 9/11 | chr4 | 127928918 | |||||||
| chr4:127929043 | C | T | 3 | a0002c0002t0005g0312 a0002c0002t0005g0313 a0002c0002t0005g0314 |
3 | HG02055.hp2 HG02976.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.998+1640G>A | MFSD8 | ENSG00000164073.11 | transcript | ENST00000641686.2 | protein_coding | 9/11 | chr4 | 127929043 | |||||||
| chr4:127929277 | C | T | 1 | a0001c0001t0001g0108 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.998+1406G>A | MFSD8 | ENSG00000164073.11 | transcript | ENST00000641686.2 | protein_coding | 9/11 | chr4 | 127929277 | |||||||
| chr4:127929306 | GAGCGAGA others(51): Show |
G | 1 | a0001c0001t0001g0116 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.998+1319_998+1376d others(60): Show |
MFSD8 | ENSG00000164073.11 | transcript | ENST00000641686.2 | protein_coding | 9/11 | chr4 | 127929306 | |||||||
| chr4:127929317 | C | T | 1 | a0001c0001t0001g0107 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.998+1366G>A | MFSD8 | ENSG00000164073.11 | transcript | ENST00000641686.2 | protein_coding | 9/11 | chr4 | 127929317 | |||||||
| chr4:127929322 | C | CA | 89 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(86): Show |
97 | HG00099.hp1 HG00140.hp2 HG00423.hp1 others(94): Show |
intron_variant | MODIFIER | c.998+1360dupT | MFSD8 | ENSG00000164073.11 | transcript | ENST00000641686.2 | protein_coding | 9/11 | chr4 | 127929322 | |||||||
| chr4:127929322 | C | CAA | 51 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(48): Show |
54 | HG00140.hp1 HG00408.hp1 HG00438.hp1 others(51): Show |
intron_variant | MODIFIER | c.998+1359_998+1360d others(4): Show |
MFSD8 | ENSG00000164073.11 | transcript | ENST00000641686.2 | protein_coding | 9/11 | chr4 | 127929322 | |||||||
| chr4:127929322 | C | CAAA | 8 | a0001c0001t0001g0107 a0001c0001t0001g0111 a0001c0001t0001g0113 others(5): Show |
8 | HG02486.hp2 HG02622.hp2 HG02630.hp1 others(5): Show |
intron_variant | MODIFIER | c.998+1358_998+1360d others(5): Show |
MFSD8 | ENSG00000164073.11 | transcript | ENST00000641686.2 | protein_coding | 9/11 | chr4 | 127929322 | |||||||
| chr4:127929322 | C | CAAAAAAA others(3): Show |
1 | a0001c0001t0022g0309 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.998+1351_998+1360d others(12): Show |
MFSD8 | ENSG00000164073.11 | transcript | ENST00000641686.2 | protein_coding | 9/11 | chr4 | 127929322 | |||||||
| chr4:127929322 | C | CAAAAAAA others(5): Show |
2 | a0001c0001t0001g0307 a0001c0009t0014g0310 |
2 | HG02451.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.998+1349_998+1360d others(14): Show |
MFSD8 | ENSG00000164073.11 | transcript | ENST00000641686.2 | protein_coding | 9/11 | chr4 | 127929322 | |||||||
| chr4:127929322 | C | CAAAAAAA others(6): Show |
6 | a0001c0001t0001g0022 a0002c0002t0003g0096 a0002c0002t0003g0098 others(3): Show |
7 | HG01168.hp2 HG02109.hp1 HG02630.hp2 others(4): Show |
intron_variant | MODIFIER | c.998+1348_998+1360d others(15): Show |
MFSD8 | ENSG00000164073.11 | transcript | ENST00000641686.2 | protein_coding | 9/11 | chr4 | 127929322 | |||||||
| chr4:127929322 | C | CAAAAAAA others(7): Show |
7 | a0001c0001t0001g0229 a0001c0001t0001g0230 a0001c0001t0001g0235 others(4): Show |
7 | HG02109.hp2 HG02258.hp1 HG02717.hp1 others(4): Show |
intron_variant | MODIFIER | c.998+1347_998+1360d others(16): Show |
MFSD8 | ENSG00000164073.11 | transcript | ENST00000641686.2 | protein_coding | 9/11 | chr4 | 127929322 | |||||||
| chr4:127929322 | C | CAAAAAAA others(8): Show |
6 | a0001c0001t0001g0023 a0001c0001t0001g0232 a0001c0001t0001g0237 others(3): Show |
6 | HG02257.hp2 HG02818.hp2 HG03139.hp2 others(3): Show |
intron_variant | MODIFIER | c.998+1346_998+1360d others(17): Show |
MFSD8 | ENSG00000164073.11 | transcript | ENST00000641686.2 | protein_coding | 9/11 | chr4 | 127929322 | |||||||
| chr4:127929322 | C | CAAAAAAA others(12): Show |
2 | a0002c0002t0003g0094 a0002c0002t0003g0095 |
2 | HG02451.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.998+1342_998+1360d others(21): Show |
MFSD8 | ENSG00000164073.11 | transcript | ENST00000641686.2 | protein_coding | 9/11 | chr4 | 127929322 | |||||||
| chr4:127929322 | C | CAAAAAAA others(18): Show |
1 | a0001c0001t0001g0236 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.998+1336_998+1360d others(27): Show |
MFSD8 | ENSG00000164073.11 | transcript | ENST00000641686.2 | protein_coding | 9/11 | chr4 | 127929322 | |||||||
| chr4:127929322 | CA | C | 10 | a0001c0001t0001g0120 a0001c0001t0001g0222 a0001c0001t0001g0223 others(7): Show |
10 | HG00099.hp2 HG00735.hp1 HG02280.hp1 others(7): Show |
intron_variant | MODIFIER | c.998+1360delT | MFSD8 | ENSG00000164073.11 | transcript | ENST00000641686.2 | protein_coding | 9/11 | chr4 | 127929322 | |||||||
| chr4:127929322 | CAAAAAAA others(6): Show |
C | 63 | a0002c0002t0002g0004 a0002c0002t0002g0008 a0002c0002t0002g0009 others(60): Show |
69 | HG00423.hp2 HG00438.hp2 HG00544.hp1 others(66): Show |
intron_variant | MODIFIER | c.998+1348_998+1360d others(15): Show |
MFSD8 | ENSG00000164073.11 | transcript | ENST00000641686.2 | protein_coding | 9/11 | chr4 | 127929322 | |||||||
| chr4:127929322 | CAAAAAAA others(7): Show |
C | 1 | a0002c0002t0002g0072 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.998+1347_998+1360d others(16): Show |
MFSD8 | ENSG00000164073.11 | transcript | ENST00000641686.2 | protein_coding | 9/11 | chr4 | 127929322 | |||||||
| chr4:127929322 | CAAAAAAA others(9): Show |
C | 1 | a0001c0001t0001g0108 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.998+1345_998+1360d others(18): Show |
MFSD8 | ENSG00000164073.11 | transcript | ENST00000641686.2 | protein_coding | 9/11 | chr4 | 127929322 | |||||||
| chr4:127929406 | G | A | 2 | a0001c0001t0001g0124 a0001c0001t0001g0126 |
2 | HG01168.hp1 HG04204.hp2 |
intron_variant | MODIFIER | c.998+1277C>T | MFSD8 | ENSG00000164073.11 | transcript | ENST00000641686.2 | protein_coding | 9/11 | chr4 | 127929406 | |||||||
| chr4:127929421 | T | TAA | 11 | a0002c0002t0003g0093 a0002c0002t0003g0094 a0002c0002t0003g0095 others(8): Show |
11 | HG02109.hp1 HG02257.hp2 HG02451.hp2 others(8): Show |
intron_variant | MODIFIER | c.998+1260_998+1261d others(4): Show |
MFSD8 | ENSG00000164073.11 | transcript | ENST00000641686.2 | protein_coding | 9/11 | chr4 | 127929421 | |||||||
| chr4:127929421 | TA | T | 9 | a0001c0001t0001g0121 a0001c0001t0001g0171 a0001c0001t0001g0224 others(6): Show |
9 | HG00558.hp2 HG01074.hp1 HG02896.hp1 others(6): Show |
intron_variant | MODIFIER | c.998+1261delT | MFSD8 | ENSG00000164073.11 | transcript | ENST00000641686.2 | protein_coding | 9/11 | chr4 | 127929421 | |||||||
| chr4:127929495 | G | A | 3 | a0002c0002t0005g0312 a0002c0002t0005g0313 a0002c0002t0005g0314 |
3 | HG02055.hp2 HG02976.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.998+1188C>T | MFSD8 | ENSG00000164073.11 | transcript | ENST00000641686.2 | protein_coding | 9/11 | chr4 | 127929495 | |||||||
| chr4:127929685 | T | C | 3 | a0002c0002t0005g0312 a0002c0002t0005g0313 a0002c0002t0005g0314 |
3 | HG02055.hp2 HG02976.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.998+998A>G | MFSD8 | ENSG00000164073.11 | transcript | ENST00000641686.2 | protein_coding | 9/11 | chr4 | 127929685 | |||||||
| chr4:127929718 | A | G | 5 | a0002c0002t0005g0312 a0002c0002t0005g0313 a0002c0002t0005g0314 others(2): Show |
6 | HG01496.hp1 HG02055.hp2 HG02572.hp1 others(3): Show |
intron_variant | MODIFIER | c.998+965T>C | MFSD8 | ENSG00000164073.11 | transcript | ENST00000641686.2 | protein_coding | 9/11 | chr4 | 127929718 | |||||||
| chr4:127929852 | G | A | 2 | a0001c0001t0001g0106 a0001c0001t0001g0131 |
2 | NA19240.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.998+831C>T | MFSD8 | ENSG00000164073.11 | transcript | ENST00000641686.2 | protein_coding | 9/11 | chr4 | 127929852 | |||||||
| chr4:127929976 | C | T | 64 | a0002c0002t0002g0004 a0002c0002t0002g0008 a0002c0002t0002g0009 others(61): Show |
70 | HG00423.hp2 HG00438.hp2 HG00544.hp1 others(67): Show |
intron_variant | MODIFIER | c.998+707G>A | MFSD8 | ENSG00000164073.11 | transcript | ENST00000641686.2 | protein_coding | 9/11 | chr4 | 127929976 | |||||||
| chr4:127930015 | G | A | 2 | a0001c0001t0001g0264 a0001c0001t0001g0269 |
2 | HG00099.hp2 HG01175.hp2 |
intron_variant | MODIFIER | c.998+668C>T | MFSD8 | ENSG00000164073.11 | transcript | ENST00000641686.2 | protein_coding | 9/11 | chr4 | 127930015 | |||||||
| chr4:127930024 | C | T | 64 | a0002c0002t0002g0004 a0002c0002t0002g0008 a0002c0002t0002g0009 others(61): Show |
70 | HG00423.hp2 HG00438.hp2 HG00544.hp1 others(67): Show |
intron_variant | MODIFIER | c.998+659G>A | MFSD8 | ENSG00000164073.11 | transcript | ENST00000641686.2 | protein_coding | 9/11 | chr4 | 127930024 | |||||||
| chr4:127930156 | G | C | 1 | a0001c0001t0001g0221 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.998+527C>G | MFSD8 | ENSG00000164073.11 | transcript | ENST00000641686.2 | protein_coding | 9/11 | chr4 | 127930156 | |||||||
| chr4:127930235 | G | A | 1 | a0001c0001t0001g0307 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.998+448C>T | MFSD8 | ENSG00000164073.11 | transcript | ENST00000641686.2 | protein_coding | 9/11 | chr4 | 127930235 | |||||||
| chr4:127930320 | A | G | 226 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(223): Show |
249 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(246): Show |
intron_variant | MODIFIER | c.998+363T>C | MFSD8 | ENSG00000164073.11 | transcript | ENST00000641686.2 | protein_coding | 9/11 | chr4 | 127930320 | |||||||
| chr4:127930833 | T | A | 1 | a0001c0001t0001g0287 | 1 | NA18980.hp1 | intron_variant | MODIFIER | c.864-16A>T | MFSD8 | ENSG00000164073.11 | transcript | ENST00000641686.2 | protein_coding | 8/11 | chr4 | 127930833 | |||||||
| chr4:127930862 | C | T | 3 | a0001c0001t0001g0106 a0001c0001t0001g0107 a0001c0001t0001g0131 |
3 | HG03486.hp2 NA19240.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.864-45G>A | MFSD8 | ENSG00000164073.11 | transcript | ENST00000641686.2 | protein_coding | 8/11 | chr4 | 127930862 | |||||||
| chr4:127930871 | T | C | 1 | a0001c0001t0001g0202 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.864-54A>G | MFSD8 | ENSG00000164073.11 | transcript | ENST00000641686.2 | protein_coding | 8/11 | chr4 | 127930871 | |||||||
| chr4:127930902 | T | G | 85 | a0002c0002t0002g0004 a0002c0002t0002g0008 a0002c0002t0002g0009 others(82): Show |
92 | HG00423.hp2 HG00438.hp2 HG00544.hp1 others(89): Show |
intron_variant | MODIFIER | c.864-85A>C | MFSD8 | ENSG00000164073.11 | transcript | ENST00000641686.2 | protein_coding | 8/11 | chr4 | 127930902 | |||||||
| chr4:127930977 | G | A | 4 | a0002c0002t0006g0089 a0002c0002t0006g0090 a0002c0002t0006g0091 others(1): Show |
4 | HG01891.hp2 HG02486.hp2 HG02622.hp2 others(1): Show |
intron_variant | MODIFIER | c.864-160C>T | MFSD8 | ENSG00000164073.11 | transcript | ENST00000641686.2 | protein_coding | 8/11 | chr4 | 127930977 | |||||||
| chr4:127931120 | C | T | 1 | a0001c0001t0001g0294 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.864-303G>A | MFSD8 | ENSG00000164073.11 | transcript | ENST00000641686.2 | protein_coding | 8/11 | chr4 | 127931120 | |||||||
| chr4:127931220 | A | C | 1 | a0001c0001t0001g0260 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.864-403T>G | MFSD8 | ENSG00000164073.11 | transcript | ENST00000641686.2 | protein_coding | 8/11 | chr4 | 127931220 | |||||||
| chr4:127931271 | T | C | 12 | a0002c0002t0003g0093 a0002c0002t0003g0094 a0002c0002t0003g0095 others(9): Show |
12 | HG02109.hp1 HG02257.hp2 HG02451.hp2 others(9): Show |
intron_variant | MODIFIER | c.864-454A>G | MFSD8 | ENSG00000164073.11 | transcript | ENST00000641686.2 | protein_coding | 8/11 | chr4 | 127931271 | |||||||
| chr4:127931354 | G | A | 1 | a0002c0002t0002g0066 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.864-537C>T | MFSD8 | ENSG00000164073.11 | transcript | ENST00000641686.2 | protein_coding | 8/11 | chr4 | 127931354 | |||||||
| chr4:127931771 | T | C | 7 | a0001c0001t0001g0222 a0001c0001t0001g0223 a0001c0001t0001g0224 others(4): Show |
7 | HG00735.hp1 HG02615.hp2 HG02723.hp1 others(4): Show |
intron_variant | MODIFIER | c.864-954A>G | MFSD8 | ENSG00000164073.11 | transcript | ENST00000641686.2 | protein_coding | 8/11 | chr4 | 127931771 | |||||||
| chr4:127931837 | G | A | 11 | a0002c0002t0003g0093 a0002c0002t0003g0094 a0002c0002t0003g0095 others(8): Show |
11 | HG02109.hp1 HG02257.hp2 HG02451.hp2 others(8): Show |
intron_variant | MODIFIER | c.864-1020C>T | MFSD8 | ENSG00000164073.11 | transcript | ENST00000641686.2 | protein_coding | 8/11 | chr4 | 127931837 | |||||||
| chr4:127931890 | C | A | 64 | a0002c0002t0002g0004 a0002c0002t0002g0008 a0002c0002t0002g0009 others(61): Show |
70 | HG00423.hp2 HG00438.hp2 HG00544.hp1 others(67): Show |
intron_variant | MODIFIER | c.864-1073G>T | MFSD8 | ENSG00000164073.11 | transcript | ENST00000641686.2 | protein_coding | 8/11 | chr4 | 127931890 | |||||||
| chr4:127931956 | A | T | 1 | a0001c0001t0001g0164 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.863+1029T>A | MFSD8 | ENSG00000164073.11 | transcript | ENST00000641686.2 | protein_coding | 8/11 | chr4 | 127931956 | |||||||
| chr4:127932060 | G | A | 1 | a0001c0001t0001g0122 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.863+925C>T | MFSD8 | ENSG00000164073.11 | transcript | ENST00000641686.2 | protein_coding | 8/11 | chr4 | 127932060 | |||||||
| chr4:127932111 | A | T | 11 | a0002c0002t0003g0093 a0002c0002t0003g0094 a0002c0002t0003g0095 others(8): Show |
11 | HG02109.hp1 HG02257.hp2 HG02451.hp2 others(8): Show |
intron_variant | MODIFIER | c.863+874T>A | MFSD8 | ENSG00000164073.11 | transcript | ENST00000641686.2 | protein_coding | 8/11 | chr4 | 127932111 | |||||||
| chr4:127932401 | C | T | 12 | a0002c0002t0003g0093 a0002c0002t0003g0094 a0002c0002t0003g0095 others(9): Show |
12 | HG02109.hp1 HG02257.hp2 HG02451.hp2 others(9): Show |
intron_variant | MODIFIER | c.863+584G>A | MFSD8 | ENSG00000164073.11 | transcript | ENST00000641686.2 | protein_coding | 8/11 | chr4 | 127932401 | |||||||
| chr4:127932647 | T | C | 2 | a0001c0005t0001g0103 a0001c0005t0001g0104 |
2 | HG02735.hp1 HG03017.hp2 |
intron_variant | MODIFIER | c.863+338A>G | MFSD8 | ENSG00000164073.11 | transcript | ENST00000641686.2 | protein_coding | 8/11 | chr4 | 127932647 | |||||||
| chr4:127932805 | C | A | 3 | a0002c0002t0005g0312 a0002c0002t0005g0313 a0002c0002t0005g0314 |
3 | HG02055.hp2 HG02976.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.863+180G>T | MFSD8 | ENSG00000164073.11 | transcript | ENST00000641686.2 | protein_coding | 8/11 | chr4 | 127932805 | |||||||
| chr4:127933199 | T | A | 2 | a0004c0004t0005g0092 a0004c0004t0010g0011 |
3 | HG01496.hp1 HG02572.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.755-106A>T | MFSD8 | ENSG00000164073.11 | transcript | ENST00000641686.2 | protein_coding | 7/11 | chr4 | 127933199 | |||||||
| chr4:127933208 | T | A | 4 | a0001c0001t0001g0120 a0001c0001t0001g0259 a0001c0001t0001g0262 others(1): Show |
4 | HG02280.hp1 HG02896.hp1 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.755-115A>T | MFSD8 | ENSG00000164073.11 | transcript | ENST00000641686.2 | protein_coding | 7/11 | chr4 | 127933208 | |||||||
| chr4:127933407 | C | T | 1 | a0001c0001t0001g0281 | 1 | NA18978.hp1 | intron_variant | MODIFIER | c.755-314G>A | MFSD8 | ENSG00000164073.11 | transcript | ENST00000641686.2 | protein_coding | 7/11 | chr4 | 127933407 | |||||||
| chr4:127933491 | G | A | 1 | a0002c0002t0012g0317 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.755-398C>T | MFSD8 | ENSG00000164073.11 | transcript | ENST00000641686.2 | protein_coding | 7/11 | chr4 | 127933491 | |||||||
| chr4:127933574 | A | G | 1 | a0001c0001t0001g0291 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.755-481T>C | MFSD8 | ENSG00000164073.11 | transcript | ENST00000641686.2 | protein_coding | 7/11 | chr4 | 127933574 | |||||||
| chr4:127933860 | A | T | 11 | a0002c0002t0003g0093 a0002c0002t0003g0094 a0002c0002t0003g0095 others(8): Show |
11 | HG02109.hp1 HG02257.hp2 HG02451.hp2 others(8): Show |
intron_variant | MODIFIER | c.755-767T>A | MFSD8 | ENSG00000164073.11 | transcript | ENST00000641686.2 | protein_coding | 7/11 | chr4 | 127933860 | |||||||
| chr4:127933905 | C | T | 1 | a0001c0009t0014g0310 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.755-812G>A | MFSD8 | ENSG00000164073.11 | transcript | ENST00000641686.2 | protein_coding | 7/11 | chr4 | 127933905 | |||||||
| chr4:127933938 | TC | T | 11 | a0002c0002t0003g0093 a0002c0002t0003g0094 a0002c0002t0003g0095 others(8): Show |
11 | HG02109.hp1 HG02257.hp2 HG02451.hp2 others(8): Show |
intron_variant | MODIFIER | c.755-846delG | MFSD8 | ENSG00000164073.11 | transcript | ENST00000641686.2 | protein_coding | 7/11 | chr4 | 127933938 | |||||||
| chr4:127933978 | C | T | 1 | a0002c0002t0002g0064 | 1 | NA18957.hp2 | intron_variant | MODIFIER | c.755-885G>A | MFSD8 | ENSG00000164073.11 | transcript | ENST00000641686.2 | protein_coding | 7/11 | chr4 | 127933978 | |||||||
| chr4:127934102 | G | T | 3 | a0002c0002t0005g0312 a0002c0002t0005g0313 a0002c0002t0005g0314 |
3 | HG02055.hp2 HG02976.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.755-1009C>A | MFSD8 | ENSG00000164073.11 | transcript | ENST00000641686.2 | protein_coding | 7/11 | chr4 | 127934102 | |||||||
| chr4:127934103 | C | T | 3 | a0002c0002t0005g0312 a0002c0002t0005g0313 a0002c0002t0005g0314 |
3 | HG02055.hp2 HG02976.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.755-1010G>A | MFSD8 | ENSG00000164073.11 | transcript | ENST00000641686.2 | protein_coding | 7/11 | chr4 | 127934103 | |||||||
| chr4:127934150 | C | T | 1 | a0001c0001t0001g0257 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.755-1057G>A | MFSD8 | ENSG00000164073.11 | transcript | ENST00000641686.2 | protein_coding | 7/11 | chr4 | 127934150 | |||||||
| chr4:127934184 | G | C | 1 | a0002c0002t0012g0317 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.755-1091C>G | MFSD8 | ENSG00000164073.11 | transcript | ENST00000641686.2 | protein_coding | 7/11 | chr4 | 127934184 | |||||||
| chr4:127934439 | A | G | 5 | a0002c0002t0005g0312 a0002c0002t0005g0313 a0002c0002t0005g0314 others(2): Show |
6 | HG01496.hp1 HG02055.hp2 HG02572.hp1 others(3): Show |
intron_variant | MODIFIER | c.755-1346T>C | MFSD8 | ENSG00000164073.11 | transcript | ENST00000641686.2 | protein_coding | 7/11 | chr4 | 127934439 | |||||||
| chr4:127934522 | T | C | 2 | a0001c0001t0001g0110 a0001c0001t0015g0112 |
2 | HG02717.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.755-1429A>G | MFSD8 | ENSG00000164073.11 | transcript | ENST00000641686.2 | protein_coding | 7/11 | chr4 | 127934522 | |||||||
| chr4:127934573 | A | AT | 19 | a0001c0001t0001g0133 a0001c0001t0001g0156 a0001c0001t0001g0160 others(16): Show |
19 | HG00741.hp2 HG01496.hp2 HG03516.hp2 others(16): Show |
intron_variant | MODIFIER | c.755-1481dupA | MFSD8 | ENSG00000164073.11 | transcript | ENST00000641686.2 | protein_coding | 7/11 | chr4 | 127934573 | |||||||
| chr4:127934573 | A | ATTT | 58 | a0002c0002t0002g0004 a0002c0002t0002g0008 a0002c0002t0002g0009 others(55): Show |
65 | HG00438.hp2 HG00544.hp1 HG00558.hp2 others(62): Show |
intron_variant | MODIFIER | c.755-1483_755-1481d others(5): Show |
MFSD8 | ENSG00000164073.11 | transcript | ENST00000641686.2 | protein_coding | 7/11 | chr4 | 127934573 | |||||||
| chr4:127934573 | A | ATTTT | 15 | a0002c0002t0002g0038 a0002c0002t0002g0051 a0002c0002t0002g0056 others(12): Show |
15 | HG00423.hp2 HG00621.hp2 HG01891.hp2 others(12): Show |
intron_variant | MODIFIER | c.755-1484_755-1481d others(6): Show |
MFSD8 | ENSG00000164073.11 | transcript | ENST00000641686.2 | protein_coding | 7/11 | chr4 | 127934573 | |||||||
| chr4:127934573 | A | ATTTTT | 9 | a0002c0002t0003g0093 a0002c0002t0003g0094 a0002c0002t0003g0095 others(6): Show |
9 | HG02109.hp1 HG02257.hp2 HG02451.hp2 others(6): Show |
intron_variant | MODIFIER | c.755-1485_755-1481d others(7): Show |
MFSD8 | ENSG00000164073.11 | transcript | ENST00000641686.2 | protein_coding | 7/11 | chr4 | 127934573 | |||||||
| chr4:127934573 | AT | A | 6 | a0001c0001t0001g0017 a0001c0001t0001g0115 a0001c0001t0001g0117 others(3): Show |
7 | HG02970.hp1 NA18950.hp1 NA18969.hp1 others(4): Show |
intron_variant | MODIFIER | c.755-1481delA | MFSD8 | ENSG00000164073.11 | transcript | ENST00000641686.2 | protein_coding | 7/11 | chr4 | 127934573 | |||||||
| chr4:127934597 | G | C | 1 | a0001c0001t0001g0221 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.755-1504C>G | MFSD8 | ENSG00000164073.11 | transcript | ENST00000641686.2 | protein_coding | 7/11 | chr4 | 127934597 | |||||||
| chr4:127934673 | G | A | 1 | a0001c0001t0001g0114 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.755-1580C>T | MFSD8 | ENSG00000164073.11 | transcript | ENST00000641686.2 | protein_coding | 7/11 | chr4 | 127934673 | |||||||
| chr4:127934731 | G | C | 64 | a0002c0002t0002g0004 a0002c0002t0002g0008 a0002c0002t0002g0009 others(61): Show |
70 | HG00423.hp2 HG00438.hp2 HG00544.hp1 others(67): Show |
intron_variant | MODIFIER | c.755-1638C>G | MFSD8 | ENSG00000164073.11 | transcript | ENST00000641686.2 | protein_coding | 7/11 | chr4 | 127934731 | |||||||
| chr4:127934907 | T | C | 1 | a0001c0001t0001g0298 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.755-1814A>G | MFSD8 | ENSG00000164073.11 | transcript | ENST00000641686.2 | protein_coding | 7/11 | chr4 | 127934907 | |||||||
| chr4:127935004 | C | T | 2 | a0001c0001t0001g0110 a0001c0001t0015g0112 |
2 | HG02717.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.755-1911G>A | MFSD8 | ENSG00000164073.11 | transcript | ENST00000641686.2 | protein_coding | 7/11 | chr4 | 127935004 | |||||||
| chr4:127935229 | T | G | 11 | a0002c0002t0003g0093 a0002c0002t0003g0094 a0002c0002t0003g0095 others(8): Show |
11 | HG02109.hp1 HG02257.hp2 HG02451.hp2 others(8): Show |
intron_variant | MODIFIER | c.755-2136A>C | MFSD8 | ENSG00000164073.11 | transcript | ENST00000641686.2 | protein_coding | 7/11 | chr4 | 127935229 | |||||||
| chr4:127935683 | A | T | 3 | a0002c0002t0005g0312 a0002c0002t0005g0313 a0002c0002t0005g0314 |
3 | HG02055.hp2 HG02976.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.755-2590T>A | MFSD8 | ENSG00000164073.11 | transcript | ENST00000641686.2 | protein_coding | 7/11 | chr4 | 127935683 | |||||||
| chr4:127935895 | A | T | 1 | a0004c0004t0005g0092 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.755-2802T>A | MFSD8 | ENSG00000164073.11 | transcript | ENST00000641686.2 | protein_coding | 7/11 | chr4 | 127935895 | |||||||
| chr4:127936071 | TTAAGTA | T | 7 | a0001c0001t0001g0012 a0001c0001t0001g0106 a0001c0001t0001g0107 others(4): Show |
8 | HG02647.hp1 HG02922.hp1 HG02965.hp2 others(5): Show |
intron_variant | MODIFIER | c.754+2706_754+2711d others(8): Show |
MFSD8 | ENSG00000164073.11 | transcript | ENST00000641686.2 | protein_coding | 7/11 | chr4 | 127936071 | |||||||
| chr4:127936103 | A | G | 1 | a0002c0002t0003g0094 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.754+2680T>C | MFSD8 | ENSG00000164073.11 | transcript | ENST00000641686.2 | protein_coding | 7/11 | chr4 | 127936103 | |||||||
| chr4:127936170 | G | A | 116 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(113): Show |
131 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(128): Show |
intron_variant | MODIFIER | c.754+2613C>T | MFSD8 | ENSG00000164073.11 | transcript | ENST00000641686.2 | protein_coding | 7/11 | chr4 | 127936170 | |||||||
| chr4:127936669 | G | A | 1 | a0001c0001t0001g0262 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.754+2114C>T | MFSD8 | ENSG00000164073.11 | transcript | ENST00000641686.2 | protein_coding | 7/11 | chr4 | 127936669 | |||||||
| chr4:127936854 | G | A | 1 | a0002c0002t0012g0317 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.754+1929C>T | MFSD8 | ENSG00000164073.11 | transcript | ENST00000641686.2 | protein_coding | 7/11 | chr4 | 127936854 | |||||||
| chr4:127936948 | G | T | 80 | a0002c0002t0002g0004 a0002c0002t0002g0008 a0002c0002t0002g0009 others(77): Show |
87 | HG00423.hp2 HG00438.hp2 HG00544.hp1 others(84): Show |
intron_variant | MODIFIER | c.754+1835C>A | MFSD8 | ENSG00000164073.11 | transcript | ENST00000641686.2 | protein_coding | 7/11 | chr4 | 127936948 | |||||||
| chr4:127937506 | T | G | 2 | a0001c0001t0001g0138 a0001c0001t0001g0167 |
2 | HG00738.hp2 HG01243.hp1 |
intron_variant | MODIFIER | c.754+1277A>C | MFSD8 | ENSG00000164073.11 | transcript | ENST00000641686.2 | protein_coding | 7/11 | chr4 | 127937506 | |||||||
| chr4:127937746 | C | G | 11 | a0002c0002t0003g0093 a0002c0002t0003g0094 a0002c0002t0003g0095 others(8): Show |
11 | HG02109.hp1 HG02257.hp2 HG02451.hp2 others(8): Show |
intron_variant | MODIFIER | c.754+1037G>C | MFSD8 | ENSG00000164073.11 | transcript | ENST00000641686.2 | protein_coding | 7/11 | chr4 | 127937746 | |||||||
| chr4:127937783 | C | T | 1 | a0003c0003t0001g0134 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.754+1000G>A | MFSD8 | ENSG00000164073.11 | transcript | ENST00000641686.2 | protein_coding | 7/11 | chr4 | 127937783 | |||||||
| chr4:127938260 | C | T | 2 | a0001c0001t0001g0241 a0001c0001t0001g0279 |
2 | HG01256.hp1 HG01258.hp1 |
intron_variant | MODIFIER | c.754+523G>A | MFSD8 | ENSG00000164073.11 | transcript | ENST00000641686.2 | protein_coding | 7/11 | chr4 | 127938260 | |||||||
| chr4:127938269 | C | T | 1 | a0002c0002t0012g0317 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.754+514G>A | MFSD8 | ENSG00000164073.11 | transcript | ENST00000641686.2 | protein_coding | 7/11 | chr4 | 127938269 | |||||||
| chr4:127938350 | G | A | 5 | a0002c0002t0002g0029 a0002c0002t0002g0064 a0002c0002t0002g0067 others(2): Show |
5 | HG02056.hp1 HG02132.hp1 NA18957.hp2 others(2): Show |
intron_variant | MODIFIER | c.754+433C>T | MFSD8 | ENSG00000164073.11 | transcript | ENST00000641686.2 | protein_coding | 7/11 | chr4 | 127938350 | |||||||
| chr4:127938433 | A | G | 1 | a0002c0002t0012g0317 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.754+350T>C | MFSD8 | ENSG00000164073.11 | transcript | ENST00000641686.2 | protein_coding | 7/11 | chr4 | 127938433 | |||||||
| chr4:127938444 | G | A | 1 | a0001c0005t0001g0103 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.754+339C>T | MFSD8 | ENSG00000164073.11 | transcript | ENST00000641686.2 | protein_coding | 7/11 | chr4 | 127938444 | |||||||
| chr4:127938456 | G | A | 3 | a0002c0002t0005g0312 a0002c0002t0005g0313 a0002c0002t0005g0314 |
3 | HG02055.hp2 HG02976.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.754+327C>T | MFSD8 | ENSG00000164073.11 | transcript | ENST00000641686.2 | protein_coding | 7/11 | chr4 | 127938456 | |||||||
| chr4:127938471 | T | C | 5 | a0002c0002t0005g0312 a0002c0002t0005g0313 a0002c0002t0005g0314 others(2): Show |
6 | HG01496.hp1 HG02055.hp2 HG02572.hp1 others(3): Show |
intron_variant | MODIFIER | c.754+312A>G | MFSD8 | ENSG00000164073.11 | transcript | ENST00000641686.2 | protein_coding | 7/11 | chr4 | 127938471 | |||||||
| chr4:127938582 | C | CA | 10 | a0001c0001t0001g0023 a0001c0001t0001g0232 a0001c0001t0001g0236 others(7): Show |
10 | HG02071.hp1 HG02717.hp1 HG02809.hp2 others(7): Show |
intron_variant | MODIFIER | c.754+200dupT | MFSD8 | ENSG00000164073.11 | transcript | ENST00000641686.2 | protein_coding | 7/11 | chr4 | 127938582 | |||||||
| chr4:127938582 | CAAA | C | 6 | a0001c0001t0001g0223 a0001c0001t0001g0224 a0001c0001t0001g0225 others(3): Show |
6 | HG00735.hp1 HG02258.hp1 HG02723.hp1 others(3): Show |
intron_variant | MODIFIER | c.754+198_754+200del others(3): Show |
MFSD8 | ENSG00000164073.11 | transcript | ENST00000641686.2 | protein_coding | 7/11 | chr4 | 127938582 | |||||||
| chr4:127938592 | A | AAAAT | 7 | a0001c0001t0001g0001 a0001c0001t0001g0018 a0001c0001t0001g0176 others(4): Show |
9 | HG01496.hp2 HG02615.hp1 HG02970.hp2 others(6): Show |
intron_variant | MODIFIER | c.754+187_754+190dup others(4): Show |
MFSD8 | ENSG00000164073.11 | transcript | ENST00000641686.2 | protein_coding | 7/11 | chr4 | 127938592 | |||||||
| chr4:127938592 | A | T | 21 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(18): Show |
22 | HG00438.hp1 HG00597.hp1 HG00741.hp2 others(19): Show |
intron_variant | MODIFIER | c.754+191T>A | MFSD8 | ENSG00000164073.11 | transcript | ENST00000641686.2 | protein_coding | 7/11 | chr4 | 127938592 | |||||||
| chr4:127938592 | AAAAT | A | 14 | a0001c0001t0001g0022 a0001c0001t0001g0108 a0001c0001t0001g0110 others(11): Show |
15 | HG00741.hp1 HG01168.hp2 HG01256.hp2 others(12): Show |
intron_variant | MODIFIER | c.754+187_754+190del others(4): Show |
MFSD8 | ENSG00000164073.11 | transcript | ENST00000641686.2 | protein_coding | 7/11 | chr4 | 127938592 | |||||||
| chr4:127938593 | AAATAAAT | A | 53 | a0001c0001t0001g0235 a0002c0002t0002g0004 a0002c0002t0002g0008 others(50): Show |
58 | HG00423.hp2 HG00438.hp2 HG00544.hp1 others(55): Show |
intron_variant | MODIFIER | c.754+183_754+189del others(7): Show |
MFSD8 | ENSG00000164073.11 | transcript | ENST00000641686.2 | protein_coding | 7/11 | chr4 | 127938593 | |||||||
| chr4:127938594 | AATAAAT | A | 7 | a0002c0002t0003g0094 a0002c0002t0003g0095 a0002c0002t0003g0096 others(4): Show |
7 | HG02109.hp1 HG02451.hp2 HG02572.hp1 others(4): Show |
intron_variant | MODIFIER | c.754+183_754+188del others(6): Show |
MFSD8 | ENSG00000164073.11 | transcript | ENST00000641686.2 | protein_coding | 7/11 | chr4 | 127938594 | |||||||
| chr4:127938595 | AT | A | 5 | a0001c0001t0001g0273 a0001c0001t0001g0292 a0001c0001t0007g0007 others(2): Show |
5 | HG01515.hp1 HG02015.hp1 NA18950.hp2 others(2): Show |
intron_variant | MODIFIER | c.754+187delA | MFSD8 | ENSG00000164073.11 | transcript | ENST00000641686.2 | protein_coding | 7/11 | chr4 | 127938595 | |||||||
| chr4:127938595 | ATAAAT | A | 13 | a0001c0001t0001g0012 a0001c0001t0001g0111 a0002c0002t0002g0046 others(10): Show |
14 | HG02257.hp2 HG02647.hp1 HG02809.hp1 others(11): Show |
intron_variant | MODIFIER | c.754+183_754+187del others(5): Show |
MFSD8 | ENSG00000164073.11 | transcript | ENST00000641686.2 | protein_coding | 7/11 | chr4 | 127938595 | |||||||
| chr4:127938596 | T | A | 76 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(73): Show |
81 | HG00099.hp2 HG00140.hp2 HG00597.hp2 others(78): Show |
intron_variant | MODIFIER | c.754+187A>T | MFSD8 | ENSG00000164073.11 | transcript | ENST00000641686.2 | protein_coding | 7/11 | chr4 | 127938596 | |||||||
| chr4:127938596 | TAAATAA | T | 4 | a0002c0002t0002g0009 a0002c0002t0005g0312 a0002c0002t0005g0313 others(1): Show |
5 | HG01496.hp1 HG02055.hp2 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.754+181_754+186del others(6): Show |
MFSD8 | ENSG00000164073.11 | transcript | ENST00000641686.2 | protein_coding | 7/11 | chr4 | 127938596 | |||||||
| chr4:127938597 | AAAT | A | 4 | a0001c0001t0001g0106 a0001c0001t0001g0107 a0001c0001t0001g0122 others(1): Show |
4 | HG03486.hp2 NA19240.hp2 NA20300.hp1 others(1): Show |
intron_variant | MODIFIER | c.754+183_754+185del others(3): Show |
MFSD8 | ENSG00000164073.11 | transcript | ENST00000641686.2 | protein_coding | 7/11 | chr4 | 127938597 | |||||||
| chr4:127938600 | T | A | 28 | a0001c0001t0001g0003 a0001c0001t0001g0022 a0001c0001t0001g0108 others(25): Show |
28 | HG00621.hp1 HG00741.hp1 HG01168.hp2 others(25): Show |
intron_variant | MODIFIER | c.754+183A>T | MFSD8 | ENSG00000164073.11 | transcript | ENST00000641686.2 | protein_coding | 7/11 | chr4 | 127938600 | |||||||
| chr4:127938602 | A | T | 8 | a0002c0002t0002g0038 a0002c0002t0002g0040 a0002c0002t0002g0043 others(5): Show |
8 | HG00423.hp2 HG03209.hp2 NA18946.hp1 others(5): Show |
intron_variant | MODIFIER | c.754+181T>A | MFSD8 | ENSG00000164073.11 | transcript | ENST00000641686.2 | protein_coding | 7/11 | chr4 | 127938602 | |||||||
| chr4:127938604 | T | A | 25 | a0001c0001t0001g0235 a0001c0001t0001g0251 a0001c0001t0001g0252 others(22): Show |
25 | HG00621.hp1 HG01891.hp2 HG02071.hp1 others(22): Show |
intron_variant | MODIFIER | c.754+179A>T | MFSD8 | ENSG00000164073.11 | transcript | ENST00000641686.2 | protein_coding | 7/11 | chr4 | 127938604 | |||||||
| chr4:127938604 | TAA | T | 7 | a0002c0002t0002g0046 a0002c0002t0002g0057 a0002c0002t0002g0059 others(4): Show |
7 | NA18939.hp2 NA18960.hp2 NA18974.hp1 others(4): Show |
intron_variant | MODIFIER | c.754+177_754+178del others(2): Show |
MFSD8 | ENSG00000164073.11 | transcript | ENST00000641686.2 | protein_coding | 7/11 | chr4 | 127938604 | |||||||
| chr4:127938606 | A | T | 58 | a0002c0002t0002g0004 a0002c0002t0002g0008 a0002c0002t0002g0009 others(55): Show |
65 | HG00423.hp2 HG00438.hp2 HG00544.hp1 others(62): Show |
intron_variant | MODIFIER | c.754+177T>A | MFSD8 | ENSG00000164073.11 | transcript | ENST00000641686.2 | protein_coding | 7/11 | chr4 | 127938606 | |||||||
| chr4:127938608 | T | A | 20 | a0001c0001t0001g0252 a0001c0001t0001g0253 a0001c0001t0001g0276 others(17): Show |
20 | HG01891.hp2 HG02109.hp1 HG02257.hp2 others(17): Show |
intron_variant | MODIFIER | c.754+175A>T | MFSD8 | ENSG00000164073.11 | transcript | ENST00000641686.2 | protein_coding | 7/11 | chr4 | 127938608 | |||||||
| chr4:127938610 | A | T | 65 | a0002c0002t0002g0004 a0002c0002t0002g0008 a0002c0002t0002g0009 others(62): Show |
72 | HG00423.hp2 HG00438.hp2 HG00544.hp1 others(69): Show |
intron_variant | MODIFIER | c.754+173T>A | MFSD8 | ENSG00000164073.11 | transcript | ENST00000641686.2 | protein_coding | 7/11 | chr4 | 127938610 | |||||||
| chr4:127938612 | TAA | T | 10 | a0002c0002t0003g0093 a0002c0002t0003g0094 a0002c0002t0003g0095 others(7): Show |
10 | HG02109.hp1 HG02257.hp2 HG02451.hp2 others(7): Show |
intron_variant | MODIFIER | c.754+169_754+170del others(2): Show |
MFSD8 | ENSG00000164073.11 | transcript | ENST00000641686.2 | protein_coding | 7/11 | chr4 | 127938612 | |||||||
| chr4:127938614 | A | T | 63 | a0002c0002t0002g0004 a0002c0002t0002g0008 a0002c0002t0002g0009 others(60): Show |
69 | HG00423.hp2 HG00438.hp2 HG00544.hp1 others(66): Show |
intron_variant | MODIFIER | c.754+169T>A | MFSD8 | ENSG00000164073.11 | transcript | ENST00000641686.2 | protein_coding | 7/11 | chr4 | 127938614 | |||||||
| chr4:127939122 | A | G | 2 | a0001c0001t0001g0168 a0001c0001t0001g0190 |
2 | HG01074.hp2 NA20752.hp2 |
intron_variant | MODIFIER | c.699-284T>C | MFSD8 | ENSG00000164073.11 | transcript | ENST00000641686.2 | protein_coding | 6/11 | chr4 | 127939122 | |||||||
| chr4:127939183 | T | A | 11 | a0002c0002t0003g0093 a0002c0002t0003g0094 a0002c0002t0003g0095 others(8): Show |
11 | HG02109.hp1 HG02257.hp2 HG02451.hp2 others(8): Show |
intron_variant | MODIFIER | c.699-345A>T | MFSD8 | ENSG00000164073.11 | transcript | ENST00000641686.2 | protein_coding | 6/11 | chr4 | 127939183 | |||||||
| chr4:127939529 | C | T | 1 | a0001c0005t0001g0104 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.698+324G>A | MFSD8 | ENSG00000164073.11 | transcript | ENST00000641686.2 | protein_coding | 6/11 | chr4 | 127939529 | |||||||
| chr4:127939586 | C | T | 5 | a0002c0002t0005g0312 a0002c0002t0005g0313 a0002c0002t0005g0314 others(2): Show |
6 | HG01496.hp1 HG02055.hp2 HG02572.hp1 others(3): Show |
intron_variant | MODIFIER | c.698+267G>A | MFSD8 | ENSG00000164073.11 | transcript | ENST00000641686.2 | protein_coding | 6/11 | chr4 | 127939586 | |||||||
| chr4:127939604 | C | CA | 8 | a0001c0001t0001g0199 a0001c0001t0001g0210 a0001c0001t0001g0211 others(5): Show |
8 | HG01358.hp1 HG01884.hp1 HG02055.hp1 others(5): Show |
intron_variant | MODIFIER | c.698+248dupT | MFSD8 | ENSG00000164073.11 | transcript | ENST00000641686.2 | protein_coding | 6/11 | chr4 | 127939604 | |||||||
| chr4:127939604 | CA | C | 180 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(177): Show |
202 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(199): Show |
intron_variant | MODIFIER | c.698+248delT | MFSD8 | ENSG00000164073.11 | transcript | ENST00000641686.2 | protein_coding | 6/11 | chr4 | 127939604 | |||||||
| chr4:127939604 | CAA | C | 54 | a0001c0001t0001g0015 a0001c0001t0001g0175 a0001c0001t0001g0202 others(51): Show |
61 | HG00423.hp2 HG00438.hp2 HG00544.hp1 others(58): Show |
intron_variant | MODIFIER | c.698+247_698+248del others(2): Show |
MFSD8 | ENSG00000164073.11 | transcript | ENST00000641686.2 | protein_coding | 6/11 | chr4 | 127939604 | |||||||
| chr4:127939604 | CAAA | C | 9 | a0002c0002t0002g0052 a0002c0002t0002g0057 a0002c0002t0005g0312 others(6): Show |
10 | HG01496.hp1 HG01891.hp2 HG02572.hp1 others(7): Show |
intron_variant | MODIFIER | c.698+246_698+248del others(3): Show |
MFSD8 | ENSG00000164073.11 | transcript | ENST00000641686.2 | protein_coding | 6/11 | chr4 | 127939604 | |||||||
| chr4:127939605 | A | C | 9 | a0001c0001t0001g0017 a0001c0001t0001g0115 a0001c0001t0001g0117 others(6): Show |
10 | HG02015.hp2 NA18946.hp2 NA18950.hp1 others(7): Show |
intron_variant | MODIFIER | c.698+248T>G | MFSD8 | ENSG00000164073.11 | transcript | ENST00000641686.2 | protein_coding | 6/11 | chr4 | 127939605 | |||||||
| chr4:127939620 | A | C | 1 | a0001c0001t0001g0214 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.698+233T>G | MFSD8 | ENSG00000164073.11 | transcript | ENST00000641686.2 | protein_coding | 6/11 | chr4 | 127939620 | |||||||
| chr4:127939624 | A | C | 1 | a0001c0001t0001g0145 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.698+229T>G | MFSD8 | ENSG00000164073.11 | transcript | ENST00000641686.2 | protein_coding | 6/11 | chr4 | 127939624 | |||||||
| chr4:127939630 | A | C | 1 | a0001c0001t0001g0147 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.698+223T>G | MFSD8 | ENSG00000164073.11 | transcript | ENST00000641686.2 | protein_coding | 6/11 | chr4 | 127939630 | |||||||
| chr4:127939639 | A | C | 1 | a0001c0001t0001g0133 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.698+214T>G | MFSD8 | ENSG00000164073.11 | transcript | ENST00000641686.2 | protein_coding | 6/11 | chr4 | 127939639 | |||||||
| chr4:127940099 | A | G | 3 | a0002c0002t0005g0312 a0002c0002t0005g0313 a0002c0002t0005g0314 |
3 | HG02055.hp2 HG02976.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.554-102T>C | MFSD8 | ENSG00000164073.11 | transcript | ENST00000641686.2 | protein_coding | 5/11 | chr4 | 127940099 | |||||||
| chr4:127940254 | G | A | 5 | a0002c0002t0005g0312 a0002c0002t0005g0313 a0002c0002t0005g0314 others(2): Show |
6 | HG01496.hp1 HG02055.hp2 HG02572.hp1 others(3): Show |
intron_variant | MODIFIER | c.554-257C>T | MFSD8 | ENSG00000164073.11 | transcript | ENST00000641686.2 | protein_coding | 5/11 | chr4 | 127940254 | |||||||
| chr4:127940422 | T | C | 59 | a0002c0002t0002g0004 a0002c0002t0002g0008 a0002c0002t0002g0009 others(56): Show |
65 | HG00423.hp2 HG00438.hp2 HG00544.hp1 others(62): Show |
intron_variant | MODIFIER | c.554-425A>G | MFSD8 | ENSG00000164073.11 | transcript | ENST00000641686.2 | protein_coding | 5/11 | chr4 | 127940422 | |||||||
| chr4:127940516 | G | GTA | 24 | a0001c0001t0001g0012 a0001c0001t0001g0106 a0001c0001t0001g0107 others(21): Show |
25 | HG00741.hp1 HG02015.hp1 HG02027.hp1 others(22): Show |
intron_variant | MODIFIER | c.554-521_554-520dup others(2): Show |
MFSD8 | ENSG00000164073.11 | transcript | ENST00000641686.2 | protein_coding | 5/11 | chr4 | 127940516 | |||||||
| chr4:127940516 | G | GTATA | 76 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(73): Show |
90 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(87): Show |
intron_variant | MODIFIER | c.554-523_554-520dup others(4): Show |
MFSD8 | ENSG00000164073.11 | transcript | ENST00000641686.2 | protein_coding | 5/11 | chr4 | 127940516 | |||||||
| chr4:127940516 | G | GTATATA | 12 | a0001c0001t0001g0026 a0001c0001t0001g0126 a0001c0001t0001g0143 others(9): Show |
12 | HG01074.hp2 HG01081.hp1 HG01168.hp1 others(9): Show |
intron_variant | MODIFIER | c.554-525_554-520dup others(6): Show |
MFSD8 | ENSG00000164073.11 | transcript | ENST00000641686.2 | protein_coding | 5/11 | chr4 | 127940516 | |||||||
| chr4:127940516 | GTA | G | 62 | a0001c0001t0001g0022 a0001c0001t0001g0281 a0001c0001t0001g0308 others(59): Show |
69 | HG00423.hp2 HG00438.hp2 HG00544.hp1 others(66): Show |
intron_variant | MODIFIER | c.554-521_554-520del others(2): Show |
MFSD8 | ENSG00000164073.11 | transcript | ENST00000641686.2 | protein_coding | 5/11 | chr4 | 127940516 | |||||||
| chr4:127940528 | ATATATAT others(7): Show |
A | 1 | a0002c0002t0012g0317 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.554-545_554-532del others(14): Show |
MFSD8 | ENSG00000164073.11 | transcript | ENST00000641686.2 | protein_coding | 5/11 | chr4 | 127940528 | |||||||
| chr4:127940534 | ATATATG | A | 2 | a0002c0002t0002g0036 a0004c0004t0010g0011 |
3 | HG01496.hp1 HG02922.hp2 NA18994.hp2 |
intron_variant | MODIFIER | c.554-543_554-538del others(6): Show |
MFSD8 | ENSG00000164073.11 | transcript | ENST00000641686.2 | protein_coding | 5/11 | chr4 | 127940534 | |||||||
| chr4:127940538 | A | ATATATAT others(3): Show |
1 | a0001c0001t0016g0177 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.554-542_554-541ins others(10): Show |
MFSD8 | ENSG00000164073.11 | transcript | ENST00000641686.2 | protein_coding | 5/11 | chr4 | 127940538 | |||||||
| chr4:127940538 | A | ATATG | 5 | a0001c0001t0001g0111 a0001c0001t0001g0158 a0001c0001t0001g0186 others(2): Show |
5 | HG01358.hp1 HG01952.hp2 HG02165.hp1 others(2): Show |
intron_variant | MODIFIER | c.554-542_554-541ins others(4): Show |
MFSD8 | ENSG00000164073.11 | transcript | ENST00000641686.2 | protein_coding | 5/11 | chr4 | 127940538 | |||||||
| chr4:127940538 | A | ATG | 4 | a0001c0001t0001g0108 a0002c0002t0003g0096 a0002c0002t0003g0098 others(1): Show |
4 | HG02109.hp1 HG02258.hp2 HG02630.hp2 others(1): Show |
intron_variant | MODIFIER | c.554-543_554-542dup others(2): Show |
MFSD8 | ENSG00000164073.11 | transcript | ENST00000641686.2 | protein_coding | 5/11 | chr4 | 127940538 | |||||||
| chr4:127940538 | A | G | 66 | a0001c0001t0001g0222 a0001c0001t0001g0226 a0002c0002t0002g0004 others(63): Show |
72 | HG00423.hp2 HG00438.hp2 HG00544.hp1 others(69): Show |
intron_variant | MODIFIER | c.554-541T>C | MFSD8 | ENSG00000164073.11 | transcript | ENST00000641686.2 | protein_coding | 5/11 | chr4 | 127940538 | |||||||
| chr4:127940540 | G | A | 3 | a0002c0002t0005g0312 a0002c0002t0005g0313 a0002c0002t0005g0314 |
3 | HG02055.hp2 HG02976.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.554-543C>T | MFSD8 | ENSG00000164073.11 | transcript | ENST00000641686.2 | protein_coding | 5/11 | chr4 | 127940540 | |||||||
| chr4:127940552 | A | G | 4 | a0002c0002t0006g0089 a0002c0002t0006g0090 a0002c0002t0006g0091 others(1): Show |
4 | HG01891.hp2 HG02486.hp2 HG02622.hp2 others(1): Show |
intron_variant | MODIFIER | c.554-555T>C | MFSD8 | ENSG00000164073.11 | transcript | ENST00000641686.2 | protein_coding | 5/11 | chr4 | 127940552 | |||||||
| chr4:127940597 | GA | G | 59 | a0002c0002t0002g0004 a0002c0002t0002g0008 a0002c0002t0002g0009 others(56): Show |
65 | HG00423.hp2 HG00438.hp2 HG00544.hp1 others(62): Show |
intron_variant | MODIFIER | c.554-601delT | MFSD8 | ENSG00000164073.11 | transcript | ENST00000641686.2 | protein_coding | 5/11 | chr4 | 127940597 | |||||||
| chr4:127940674 | A | G | 1 | a0001c0001t0001g0271 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.554-677T>C | MFSD8 | ENSG00000164073.11 | transcript | ENST00000641686.2 | protein_coding | 5/11 | chr4 | 127940674 | |||||||
| chr4:127940714 | T | TAAAGAAA others(309): Show |
1 | a0002c0002t0003g0099 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.554-718_554-717ins others(316): Show |
MFSD8 | ENSG00000164073.11 | transcript | ENST00000641686.2 | protein_coding | 5/11 | chr4 | 127940714 | |||||||
| chr4:127940714 | T | TAAAGAAA others(315): Show |
2 | a0002c0002t0003g0094 a0002c0002t0003g0095 |
2 | HG02451.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.554-718_554-717ins others(322): Show |
MFSD8 | ENSG00000164073.11 | transcript | ENST00000641686.2 | protein_coding | 5/11 | chr4 | 127940714 | |||||||
| chr4:127940714 | T | TAAAGAAA others(319): Show |
2 | a0002c0002t0003g0098 a0002c0002t0003g0316 |
2 | HG02630.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.554-718_554-717ins others(326): Show |
MFSD8 | ENSG00000164073.11 | transcript | ENST00000641686.2 | protein_coding | 5/11 | chr4 | 127940714 | |||||||
| chr4:127940714 | T | TAAAGAAA others(320): Show |
3 | a0002c0002t0003g0096 a0002c0002t0003g0101 a0002c0002t0003g0102 |
3 | HG02109.hp1 HG02818.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.554-718_554-717ins others(327): Show |
MFSD8 | ENSG00000164073.11 | transcript | ENST00000641686.2 | protein_coding | 5/11 | chr4 | 127940714 | |||||||
| chr4:127940714 | T | TAAAGAAA others(321): Show |
1 | a0002c0002t0003g0100 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.554-718_554-717ins others(328): Show |
MFSD8 | ENSG00000164073.11 | transcript | ENST00000641686.2 | protein_coding | 5/11 | chr4 | 127940714 | |||||||
| chr4:127940714 | T | TAAAGAAA others(322): Show |
2 | a0002c0002t0003g0093 a0002c0002t0003g0097 |
2 | HG02257.hp2 HG02886.hp1 |
intron_variant | MODIFIER | c.554-718_554-717ins others(329): Show |
MFSD8 | ENSG00000164073.11 | transcript | ENST00000641686.2 | protein_coding | 5/11 | chr4 | 127940714 | |||||||
| chr4:127940955 | T | C | 311 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(308): Show |
346 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(343): Show |
intron_variant | MODIFIER | c.554-958A>G | MFSD8 | ENSG00000164073.11 | transcript | ENST00000641686.2 | protein_coding | 5/11 | chr4 | 127940955 | |||||||
| chr4:127941026 | T | G | 4 | a0002c0002t0006g0089 a0002c0002t0006g0090 a0002c0002t0006g0091 others(1): Show |
4 | HG01891.hp2 HG02486.hp2 HG02622.hp2 others(1): Show |
intron_variant | MODIFIER | c.553+1019A>C | MFSD8 | ENSG00000164073.11 | transcript | ENST00000641686.2 | protein_coding | 5/11 | chr4 | 127941026 | |||||||
| chr4:127941134 | T | C | 1 | a0001c0001t0001g0288 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.553+911A>G | MFSD8 | ENSG00000164073.11 | transcript | ENST00000641686.2 | protein_coding | 5/11 | chr4 | 127941134 | |||||||
| chr4:127941348 | A | T | 11 | a0002c0002t0003g0093 a0002c0002t0003g0094 a0002c0002t0003g0095 others(8): Show |
11 | HG02109.hp1 HG02257.hp2 HG02451.hp2 others(8): Show |
intron_variant | MODIFIER | c.553+697T>A | MFSD8 | ENSG00000164073.11 | transcript | ENST00000641686.2 | protein_coding | 5/11 | chr4 | 127941348 | |||||||
| chr4:127941493 | G | A | 1 | a0001c0001t0001g0219 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.553+552C>T | MFSD8 | ENSG00000164073.11 | transcript | ENST00000641686.2 | protein_coding | 5/11 | chr4 | 127941493 | |||||||
| chr4:127941544 | C | T | 2 | a0001c0001t0001g0110 a0001c0001t0015g0112 |
2 | HG02717.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.553+501G>A | MFSD8 | ENSG00000164073.11 | transcript | ENST00000641686.2 | protein_coding | 5/11 | chr4 | 127941544 | |||||||
| chr4:127941588 | A | G | 1 | a0001c0001t0001g0127 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.553+457T>C | MFSD8 | ENSG00000164073.11 | transcript | ENST00000641686.2 | protein_coding | 5/11 | chr4 | 127941588 | |||||||
| chr4:127941688 | C | T | 4 | a0002c0002t0006g0089 a0002c0002t0006g0090 a0002c0002t0006g0091 others(1): Show |
4 | HG01891.hp2 HG02486.hp2 HG02622.hp2 others(1): Show |
intron_variant | MODIFIER | c.553+357G>A | MFSD8 | ENSG00000164073.11 | transcript | ENST00000641686.2 | protein_coding | 5/11 | chr4 | 127941688 | |||||||
| chr4:127941850 | G | C | 1 | a0001c0001t0022g0309 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.553+195C>G | MFSD8 | ENSG00000164073.11 | transcript | ENST00000641686.2 | protein_coding | 5/11 | chr4 | 127941850 | |||||||
| chr4:127941894 | G | C | 59 | a0002c0002t0002g0004 a0002c0002t0002g0008 a0002c0002t0002g0009 others(56): Show |
65 | HG00423.hp2 HG00438.hp2 HG00544.hp1 others(62): Show |
intron_variant | MODIFIER | c.553+151C>G | MFSD8 | ENSG00000164073.11 | transcript | ENST00000641686.2 | protein_coding | 5/11 | chr4 | 127941894 | |||||||
| chr4:127942306 | G | C | 5 | a0002c0002t0005g0312 a0002c0002t0005g0313 a0002c0002t0005g0314 others(2): Show |
6 | HG01496.hp1 HG02055.hp2 HG02572.hp1 others(3): Show |
intron_variant | MODIFIER | c.440-148C>G | MFSD8 | ENSG00000164073.11 | transcript | ENST00000641686.2 | protein_coding | 4/11 | chr4 | 127942306 | |||||||
| chr4:127942416 | C | T | 1 | a0002c0002t0012g0317 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.440-258G>A | MFSD8 | ENSG00000164073.11 | transcript | ENST00000641686.2 | protein_coding | 4/11 | chr4 | 127942416 | |||||||
| chr4:127942458 | G | T | 3 | a0001c0001t0001g0209 a0001c0001t0001g0210 a0001c0001t0001g0211 |
3 | HG01884.hp1 HG02055.hp1 HG02647.hp2 |
intron_variant | MODIFIER | c.440-300C>A | MFSD8 | ENSG00000164073.11 | transcript | ENST00000641686.2 | protein_coding | 4/11 | chr4 | 127942458 | |||||||
| chr4:127942753 | A | T | 1 | a0001c0001t0001g0114 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.440-595T>A | MFSD8 | ENSG00000164073.11 | transcript | ENST00000641686.2 | protein_coding | 4/11 | chr4 | 127942753 | |||||||
| chr4:127942776 | C | T | 2 | a0001c0001t0001g0290 a0001c0001t0001g0295 |
2 | HG01175.hp1 HG01346.hp1 |
intron_variant | MODIFIER | c.440-618G>A | MFSD8 | ENSG00000164073.11 | transcript | ENST00000641686.2 | protein_coding | 4/11 | chr4 | 127942776 | |||||||
| chr4:127942985 | G | A | 4 | a0002c0002t0006g0089 a0002c0002t0006g0090 a0002c0002t0006g0091 others(1): Show |
4 | HG01891.hp2 HG02486.hp2 HG02622.hp2 others(1): Show |
intron_variant | MODIFIER | c.439+767C>T | MFSD8 | ENSG00000164073.11 | transcript | ENST00000641686.2 | protein_coding | 4/11 | chr4 | 127942985 | |||||||
| chr4:127943000 | C | T | 1 | a0002c0002t0005g0314 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.439+752G>A | MFSD8 | ENSG00000164073.11 | transcript | ENST00000641686.2 | protein_coding | 4/11 | chr4 | 127943000 | |||||||
| chr4:127943045 | C | T | 11 | a0002c0002t0003g0093 a0002c0002t0003g0094 a0002c0002t0003g0095 others(8): Show |
11 | HG02109.hp1 HG02257.hp2 HG02451.hp2 others(8): Show |
intron_variant | MODIFIER | c.439+707G>A | MFSD8 | ENSG00000164073.11 | transcript | ENST00000641686.2 | protein_coding | 4/11 | chr4 | 127943045 | |||||||
| chr4:127943211 | C | A | 39 | a0001c0001t0001g0002 a0001c0001t0001g0021 a0001c0001t0001g0214 others(36): Show |
46 | HG00408.hp2 HG00597.hp1 HG00639.hp2 others(43): Show |
intron_variant | MODIFIER | c.439+541G>T | MFSD8 | ENSG00000164073.11 | transcript | ENST00000641686.2 | protein_coding | 4/11 | chr4 | 127943211 | |||||||
| chr4:127943212 | C | A | 39 | a0001c0001t0001g0002 a0001c0001t0001g0021 a0001c0001t0001g0214 others(36): Show |
46 | HG00408.hp2 HG00597.hp1 HG00639.hp2 others(43): Show |
intron_variant | MODIFIER | c.439+540G>T | MFSD8 | ENSG00000164073.11 | transcript | ENST00000641686.2 | protein_coding | 4/11 | chr4 | 127943212 | |||||||
| chr4:127943217 | CA | C | 15 | a0001c0001t0001g0129 a0001c0001t0001g0234 a0001c0001t0001g0299 others(12): Show |
15 | HG02109.hp1 HG02257.hp2 HG02630.hp2 others(12): Show |
intron_variant | MODIFIER | c.439+534delT | MFSD8 | ENSG00000164073.11 | transcript | ENST00000641686.2 | protein_coding | 4/11 | chr4 | 127943217 | |||||||
| chr4:127943279 | AGCAAGTG others(63): Show |
A | 1 | a0001c0001t0001g0108 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.439+403_439+472del others(70): Show |
MFSD8 | ENSG00000164073.11 | transcript | ENST00000641686.2 | protein_coding | 4/11 | chr4 | 127943279 | |||||||
| chr4:127943326 | C | T | 1 | a0001c0001t0001g0198 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.439+426G>A | MFSD8 | ENSG00000164073.11 | transcript | ENST00000641686.2 | protein_coding | 4/11 | chr4 | 127943326 | |||||||
| chr4:127943390 | G | GT | 7 | a0001c0001t0001g0156 a0001c0001t0001g0193 a0001c0001t0001g0286 others(4): Show |
7 | HG00597.hp2 HG01175.hp1 HG02970.hp1 others(4): Show |
intron_variant | MODIFIER | c.439+361dupA | MFSD8 | ENSG00000164073.11 | transcript | ENST00000641686.2 | protein_coding | 4/11 | chr4 | 127943390 | |||||||
| chr4:127943501 | C | T | 1 | a0001c0001t0001g0170 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.439+251G>A | MFSD8 | ENSG00000164073.11 | transcript | ENST00000641686.2 | protein_coding | 4/11 | chr4 | 127943501 | |||||||
| chr4:127943638 | T | A | 1 | a0002c0002t0002g0038 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.439+114A>T | MFSD8 | ENSG00000164073.11 | transcript | ENST00000641686.2 | protein_coding | 4/11 | chr4 | 127943638 | |||||||
| chr4:127943648 | T | C | 4 | a0002c0002t0006g0089 a0002c0002t0006g0090 a0002c0002t0006g0091 others(1): Show |
4 | HG01891.hp2 HG02486.hp2 HG02622.hp2 others(1): Show |
intron_variant | MODIFIER | c.439+104A>G | MFSD8 | ENSG00000164073.11 | transcript | ENST00000641686.2 | protein_coding | 4/11 | chr4 | 127943648 | |||||||
| chr4:127943671 | G | A | 2 | a0001c0001t0001g0241 a0001c0001t0001g0279 |
2 | HG01256.hp1 HG01258.hp1 |
intron_variant | MODIFIER | c.439+81C>T | MFSD8 | ENSG00000164073.11 | transcript | ENST00000641686.2 | protein_coding | 4/11 | chr4 | 127943671 | |||||||
| chr4:127944000 | A | G | 1 | a0002c0002t0012g0317 | 1 | HG02486.hp1 | splice_region_variant&intron_variant | LOW | c.199-8T>C | MFSD8 | ENSG00000164073.11 | transcript | ENST00000641686.2 | protein_coding | 3/11 | chr4 | 127944000 | |||||||
| chr4:127944116 | A | G | 11 | a0002c0002t0003g0093 a0002c0002t0003g0094 a0002c0002t0003g0095 others(8): Show |
11 | HG02109.hp1 HG02257.hp2 HG02451.hp2 others(8): Show |
intron_variant | MODIFIER | c.199-124T>C | MFSD8 | ENSG00000164073.11 | transcript | ENST00000641686.2 | protein_coding | 3/11 | chr4 | 127944116 | |||||||
| chr4:127944409 | T | A | 2 | a0002c0002t0002g0040 a0002c0002t0002g0043 |
2 | NA18984.hp1 NA19085.hp2 |
intron_variant | MODIFIER | c.199-417A>T | MFSD8 | ENSG00000164073.11 | transcript | ENST00000641686.2 | protein_coding | 3/11 | chr4 | 127944409 | |||||||
| chr4:127944473 | C | T | 5 | a0002c0002t0003g0093 a0002c0002t0003g0097 a0002c0002t0003g0099 others(2): Show |
5 | HG02257.hp2 HG02809.hp1 HG02818.hp1 others(2): Show |
intron_variant | MODIFIER | c.199-481G>A | MFSD8 | ENSG00000164073.11 | transcript | ENST00000641686.2 | protein_coding | 3/11 | chr4 | 127944473 | |||||||
| chr4:127944489 | C | A | 2 | a0004c0004t0005g0092 a0004c0004t0010g0011 |
3 | HG01496.hp1 HG02572.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.199-497G>T | MFSD8 | ENSG00000164073.11 | transcript | ENST00000641686.2 | protein_coding | 3/11 | chr4 | 127944489 | |||||||
| chr4:127944509 | T | C | 1 | a0001c0001t0001g0107 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.199-517A>G | MFSD8 | ENSG00000164073.11 | transcript | ENST00000641686.2 | protein_coding | 3/11 | chr4 | 127944509 | |||||||
| chr4:127944666 | T | A | 1 | a0001c0001t0001g0221 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.199-674A>T | MFSD8 | ENSG00000164073.11 | transcript | ENST00000641686.2 | protein_coding | 3/11 | chr4 | 127944666 | |||||||
| chr4:127944668 | A | T | 1 | a0001c0001t0001g0221 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.199-676T>A | MFSD8 | ENSG00000164073.11 | transcript | ENST00000641686.2 | protein_coding | 3/11 | chr4 | 127944668 | |||||||
| chr4:127944900 | T | G | 207 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(204): Show |
230 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(227): Show |
intron_variant | MODIFIER | c.199-908A>C | MFSD8 | ENSG00000164073.11 | transcript | ENST00000641686.2 | protein_coding | 3/11 | chr4 | 127944900 | |||||||
| chr4:127944983 | G | A | 1 | a0002c0002t0003g0102 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.199-991C>T | MFSD8 | ENSG00000164073.11 | transcript | ENST00000641686.2 | protein_coding | 3/11 | chr4 | 127944983 | |||||||
| chr4:127945007 | C | A | 1 | a0001c0001t0001g0153 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.199-1015G>T | MFSD8 | ENSG00000164073.11 | transcript | ENST00000641686.2 | protein_coding | 3/11 | chr4 | 127945007 | |||||||
| chr4:127945437 | C | A | 1 | a0001c0001t0001g0108 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.199-1445G>T | MFSD8 | ENSG00000164073.11 | transcript | ENST00000641686.2 | protein_coding | 3/11 | chr4 | 127945437 | |||||||
| chr4:127945498 | T | A | 1 | a0001c0001t0001g0275 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.199-1506A>T | MFSD8 | ENSG00000164073.11 | transcript | ENST00000641686.2 | protein_coding | 3/11 | chr4 | 127945498 | |||||||
| chr4:127945514 | G | A | 1 | a0002c0002t0002g0069 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.199-1522C>T | MFSD8 | ENSG00000164073.11 | transcript | ENST00000641686.2 | protein_coding | 3/11 | chr4 | 127945514 | |||||||
| chr4:127945530 | G | A | 2 | a0001c0001t0016g0177 a0001c0001t0018g0196 |
2 | HG03139.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.199-1538C>T | MFSD8 | ENSG00000164073.11 | transcript | ENST00000641686.2 | protein_coding | 3/11 | chr4 | 127945530 | |||||||
| chr4:127945761 | C | T | 2 | a0001c0001t0001g0144 a0001c0001t0001g0155 |
2 | HG01257.hp1 HG01516.hp1 |
intron_variant | MODIFIER | c.199-1769G>A | MFSD8 | ENSG00000164073.11 | transcript | ENST00000641686.2 | protein_coding | 3/11 | chr4 | 127945761 | |||||||
| chr4:127945918 | C | CT | 6 | a0001c0001t0001g0169 a0001c0001t0001g0261 a0001c0001t0001g0290 others(3): Show |
6 | HG01346.hp1 HG01978.hp1 HG02080.hp2 others(3): Show |
intron_variant | MODIFIER | c.199-1927dupA | MFSD8 | ENSG00000164073.11 | transcript | ENST00000641686.2 | protein_coding | 3/11 | chr4 | 127945918 | |||||||
| chr4:127946126 | C | G | 1 | a0001c0001t0001g0219 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.199-2134G>C | MFSD8 | ENSG00000164073.11 | transcript | ENST00000641686.2 | protein_coding | 3/11 | chr4 | 127946126 | |||||||
| chr4:127946150 | C | G | 1 | a0001c0001t0001g0194 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.199-2158G>C | MFSD8 | ENSG00000164073.11 | transcript | ENST00000641686.2 | protein_coding | 3/11 | chr4 | 127946150 | |||||||
| chr4:127946173 | A | G | 11 | a0002c0002t0003g0093 a0002c0002t0003g0094 a0002c0002t0003g0095 others(8): Show |
11 | HG02109.hp1 HG02257.hp2 HG02451.hp2 others(8): Show |
intron_variant | MODIFIER | c.199-2181T>C | MFSD8 | ENSG00000164073.11 | transcript | ENST00000641686.2 | protein_coding | 3/11 | chr4 | 127946173 | |||||||
| chr4:127946211 | G | A | 1 | a0002c0002t0002g0078 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.199-2219C>T | MFSD8 | ENSG00000164073.11 | transcript | ENST00000641686.2 | protein_coding | 3/11 | chr4 | 127946211 | |||||||
| chr4:127946457 | T | C | 7 | a0001c0001t0001g0222 a0001c0001t0001g0223 a0001c0001t0001g0224 others(4): Show |
7 | HG00735.hp1 HG02615.hp2 HG02723.hp1 others(4): Show |
intron_variant | MODIFIER | c.199-2465A>G | MFSD8 | ENSG00000164073.11 | transcript | ENST00000641686.2 | protein_coding | 3/11 | chr4 | 127946457 | |||||||
| chr4:127946836 | A | G | 4 | a0002c0002t0006g0089 a0002c0002t0006g0090 a0002c0002t0006g0091 others(1): Show |
4 | HG01891.hp2 HG02486.hp2 HG02622.hp2 others(1): Show |
intron_variant | MODIFIER | c.199-2844T>C | MFSD8 | ENSG00000164073.11 | transcript | ENST00000641686.2 | protein_coding | 3/11 | chr4 | 127946836 | |||||||
| chr4:127946915 | C | CA | 7 | a0001c0001t0001g0206 a0001c0001t0001g0241 a0001c0001t0001g0249 others(4): Show |
7 | HG01175.hp2 HG01256.hp1 NA18943.hp2 others(4): Show |
intron_variant | MODIFIER | c.198+2888dupT | MFSD8 | ENSG00000164073.11 | transcript | ENST00000641686.2 | protein_coding | 3/11 | chr4 | 127946915 | |||||||
| chr4:127946923 | A | C | 1 | a0001c0001t0001g0268 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.198+2881T>G | MFSD8 | ENSG00000164073.11 | transcript | ENST00000641686.2 | protein_coding | 3/11 | chr4 | 127946923 | |||||||
| chr4:127946934 | T | TA | 13 | a0001c0001t0001g0295 a0002c0002t0003g0093 a0002c0002t0003g0094 others(10): Show |
13 | HG01175.hp1 HG02056.hp2 HG02109.hp1 others(10): Show |
intron_variant | MODIFIER | c.198+2869dupT | MFSD8 | ENSG00000164073.11 | transcript | ENST00000641686.2 | protein_coding | 3/11 | chr4 | 127946934 | |||||||
| chr4:127946984 | G | A | 1 | a0001c0001t0001g0266 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.198+2820C>T | MFSD8 | ENSG00000164073.11 | transcript | ENST00000641686.2 | protein_coding | 3/11 | chr4 | 127946984 | |||||||
| chr4:127947089 | G | C | 1 | a0001c0001t0001g0266 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.198+2715C>G | MFSD8 | ENSG00000164073.11 | transcript | ENST00000641686.2 | protein_coding | 3/11 | chr4 | 127947089 | |||||||
| chr4:127947103 | C | G | 16 | a0002c0002t0003g0093 a0002c0002t0003g0094 a0002c0002t0003g0095 others(13): Show |
16 | HG01891.hp2 HG02109.hp1 HG02257.hp2 others(13): Show |
intron_variant | MODIFIER | c.198+2701G>C | MFSD8 | ENSG00000164073.11 | transcript | ENST00000641686.2 | protein_coding | 3/11 | chr4 | 127947103 | |||||||
| chr4:127947195 | G | T | 3 | a0002c0002t0005g0312 a0002c0002t0005g0313 a0002c0002t0005g0314 |
3 | HG02055.hp2 HG02976.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.198+2609C>A | MFSD8 | ENSG00000164073.11 | transcript | ENST00000641686.2 | protein_coding | 3/11 | chr4 | 127947195 | |||||||
| chr4:127947299 | T | A | 85 | a0002c0002t0002g0004 a0002c0002t0002g0008 a0002c0002t0002g0009 others(82): Show |
92 | HG00423.hp2 HG00438.hp2 HG00544.hp1 others(89): Show |
intron_variant | MODIFIER | c.198+2505A>T | MFSD8 | ENSG00000164073.11 | transcript | ENST00000641686.2 | protein_coding | 3/11 | chr4 | 127947299 | |||||||
| chr4:127947347 | G | A | 1 | a0001c0001t0001g0147 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.198+2457C>T | MFSD8 | ENSG00000164073.11 | transcript | ENST00000641686.2 | protein_coding | 3/11 | chr4 | 127947347 | |||||||
| chr4:127947577 | C | CA | 27 | a0001c0001t0001g0176 a0001c0001t0001g0282 a0001c0001t0001g0294 others(24): Show |
27 | HG01496.hp2 HG01891.hp2 HG02109.hp1 others(24): Show |
intron_variant | MODIFIER | c.198+2226dupT | MFSD8 | ENSG00000164073.11 | transcript | ENST00000641686.2 | protein_coding | 3/11 | chr4 | 127947577 | |||||||
| chr4:127947693 | G | A | 1 | a0001c0001t0001g0114 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.198+2111C>T | MFSD8 | ENSG00000164073.11 | transcript | ENST00000641686.2 | protein_coding | 3/11 | chr4 | 127947693 | |||||||
| chr4:127947857 | C | T | 4 | a0002c0002t0006g0089 a0002c0002t0006g0090 a0002c0002t0006g0091 others(1): Show |
4 | HG01891.hp2 HG02486.hp2 HG02622.hp2 others(1): Show |
intron_variant | MODIFIER | c.198+1947G>A | MFSD8 | ENSG00000164073.11 | transcript | ENST00000641686.2 | protein_coding | 3/11 | chr4 | 127947857 | |||||||
| chr4:127947858 | G | A | 1 | a0003c0003t0001g0200 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.198+1946C>T | MFSD8 | ENSG00000164073.11 | transcript | ENST00000641686.2 | protein_coding | 3/11 | chr4 | 127947858 | |||||||
| chr4:127947863 | A | AAC | 102 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(99): Show |
115 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(112): Show |
intron_variant | MODIFIER | c.198+1939_198+1940d others(4): Show |
MFSD8 | ENSG00000164073.11 | transcript | ENST00000641686.2 | protein_coding | 3/11 | chr4 | 127947863 | |||||||
| chr4:127947863 | A | AACAC | 14 | a0001c0001t0001g0014 a0001c0001t0001g0108 a0001c0001t0001g0113 others(11): Show |
15 | HG01081.hp1 HG01256.hp2 HG01358.hp1 others(12): Show |
intron_variant | MODIFIER | c.198+1937_198+1940d others(6): Show |
MFSD8 | ENSG00000164073.11 | transcript | ENST00000641686.2 | protein_coding | 3/11 | chr4 | 127947863 | |||||||
| chr4:127947863 | A | AACACAC | 4 | a0001c0001t0001g0114 a0001c0001t0001g0270 a0001c0001t0015g0112 others(1): Show |
4 | HG02109.hp1 HG02717.hp2 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.198+1935_198+1940d others(8): Show |
MFSD8 | ENSG00000164073.11 | transcript | ENST00000641686.2 | protein_coding | 3/11 | chr4 | 127947863 | |||||||
| chr4:127947863 | AAC | A | 11 | a0001c0001t0001g0022 a0001c0001t0001g0263 a0001c0001t0001g0264 others(8): Show |
12 | HG00099.hp2 HG01168.hp2 HG02280.hp2 others(9): Show |
intron_variant | MODIFIER | c.198+1939_198+1940d others(4): Show |
MFSD8 | ENSG00000164073.11 | transcript | ENST00000641686.2 | protein_coding | 3/11 | chr4 | 127947863 | |||||||
| chr4:127947863 | AACAC | A | 3 | a0001c0001t0001g0305 a0001c0009t0014g0310 a0004c0004t0010g0011 |
4 | HG01496.hp1 HG02451.hp1 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.198+1937_198+1940d others(6): Show |
MFSD8 | ENSG00000164073.11 | transcript | ENST00000641686.2 | protein_coding | 3/11 | chr4 | 127947863 | |||||||
| chr4:127947863 | AACACACA others(15): Show |
A | 4 | a0002c0002t0006g0089 a0002c0002t0006g0090 a0002c0002t0006g0091 others(1): Show |
4 | HG01891.hp2 HG02486.hp2 HG02622.hp2 others(1): Show |
intron_variant | MODIFIER | c.198+1919_198+1940d others(24): Show |
MFSD8 | ENSG00000164073.11 | transcript | ENST00000641686.2 | protein_coding | 3/11 | chr4 | 127947863 | |||||||
| chr4:127947898 | A | ACACACAC others(11): Show |
5 | a0002c0002t0002g0046 a0002c0002t0002g0057 a0002c0002t0002g0059 others(2): Show |
5 | NA18939.hp2 NA18960.hp2 NA18974.hp1 others(2): Show |
intron_variant | MODIFIER | c.198+1905_198+1906i others(20): Show |
MFSD8 | ENSG00000164073.11 | transcript | ENST00000641686.2 | protein_coding | 3/11 | chr4 | 127947898 | |||||||
| chr4:127947898 | A | ACACACAC others(9): Show |
2 | a0002c0002t0002g0061 a0002c0002t0002g0078 |
2 | NA18983.hp1 NA19091.hp2 |
intron_variant | MODIFIER | c.198+1905_198+1906i others(18): Show |
MFSD8 | ENSG00000164073.11 | transcript | ENST00000641686.2 | protein_coding | 3/11 | chr4 | 127947898 | |||||||
| chr4:127947898 | A | ACACACAC others(7): Show |
1 | a0002c0002t0002g0009 | 2 | NA18747.hp2 NA18968.hp2 |
intron_variant | MODIFIER | c.198+1905_198+1906i others(16): Show |
MFSD8 | ENSG00000164073.11 | transcript | ENST00000641686.2 | protein_coding | 3/11 | chr4 | 127947898 | |||||||
| chr4:127947898 | A | ACACACAC others(5): Show |
6 | a0002c0002t0002g0032 a0002c0002t0002g0036 a0002c0002t0002g0062 others(3): Show |
6 | HG01978.hp2 NA18946.hp1 NA18947.hp1 others(3): Show |
intron_variant | MODIFIER | c.198+1905_198+1906i others(14): Show |
MFSD8 | ENSG00000164073.11 | transcript | ENST00000641686.2 | protein_coding | 3/11 | chr4 | 127947898 | |||||||
| chr4:127947898 | A | ACACACAC others(3): Show |
34 | a0002c0002t0002g0004 a0002c0002t0002g0038 a0002c0002t0002g0040 others(31): Show |
37 | HG00558.hp2 HG00597.hp2 HG00621.hp2 others(34): Show |
intron_variant | MODIFIER | c.198+1905_198+1906i others(12): Show |
MFSD8 | ENSG00000164073.11 | transcript | ENST00000641686.2 | protein_coding | 3/11 | chr4 | 127947898 | |||||||
| chr4:127947898 | A | ACACACT | 8 | a0002c0002t0003g0093 a0002c0002t0003g0097 a0002c0002t0003g0098 others(5): Show |
8 | HG02257.hp2 HG02630.hp2 HG02809.hp1 others(5): Show |
intron_variant | MODIFIER | c.198+1905_198+1906i others(8): Show |
MFSD8 | ENSG00000164073.11 | transcript | ENST00000641686.2 | protein_coding | 3/11 | chr4 | 127947898 | |||||||
| chr4:127947898 | A | ACACACTC others(1): Show |
9 | a0002c0002t0002g0010 a0002c0002t0002g0029 a0002c0002t0002g0037 others(6): Show |
10 | HG00423.hp2 HG00544.hp1 HG00609.hp2 others(7): Show |
intron_variant | MODIFIER | c.198+1905_198+1906i others(10): Show |
MFSD8 | ENSG00000164073.11 | transcript | ENST00000641686.2 | protein_coding | 3/11 | chr4 | 127947898 | |||||||
| chr4:127947898 | A | ACACTCT | 7 | a0002c0002t0002g0008 a0002c0002t0002g0031 a0002c0002t0002g0039 others(4): Show |
8 | HG00438.hp2 NA18942.hp2 NA18943.hp2 others(5): Show |
intron_variant | MODIFIER | c.198+1905_198+1906i others(8): Show |
MFSD8 | ENSG00000164073.11 | transcript | ENST00000641686.2 | protein_coding | 3/11 | chr4 | 127947898 | |||||||
| chr4:127947898 | A | T | 2 | a0002c0002t0003g0094 a0002c0002t0003g0095 |
2 | HG02451.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.198+1906T>A | MFSD8 | ENSG00000164073.11 | transcript | ENST00000641686.2 | protein_coding | 3/11 | chr4 | 127947898 | |||||||
| chr4:127947898 | ACT | A | 4 | a0001c0001t0001g0142 a0001c0001t0001g0175 a0001c0001t0001g0176 others(1): Show |
4 | HG01496.hp2 HG02602.hp2 HG03704.hp1 others(1): Show |
intron_variant | MODIFIER | c.198+1904_198+1905d others(4): Show |
MFSD8 | ENSG00000164073.11 | transcript | ENST00000641686.2 | protein_coding | 3/11 | chr4 | 127947898 | |||||||
| chr4:127947900 | T | A | 112 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(109): Show |
127 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(124): Show |
intron_variant | MODIFIER | c.198+1904A>T | MFSD8 | ENSG00000164073.11 | transcript | ENST00000641686.2 | protein_coding | 3/11 | chr4 | 127947900 | |||||||
| chr4:127947934 | A | G | 1 | a0001c0001t0001g0124 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.198+1870T>C | MFSD8 | ENSG00000164073.11 | transcript | ENST00000641686.2 | protein_coding | 3/11 | chr4 | 127947934 | |||||||
| chr4:127948234 | C | T | 1 | a0001c0001t0001g0127 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.198+1570G>A | MFSD8 | ENSG00000164073.11 | transcript | ENST00000641686.2 | protein_coding | 3/11 | chr4 | 127948234 | |||||||
| chr4:127948245 | G | A | 2 | a0001c0001t0016g0177 a0001c0001t0018g0196 |
2 | HG03139.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.198+1559C>T | MFSD8 | ENSG00000164073.11 | transcript | ENST00000641686.2 | protein_coding | 3/11 | chr4 | 127948245 | |||||||
| chr4:127948479 | T | C | 1 | a0001c0001t0001g0201 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.198+1325A>G | MFSD8 | ENSG00000164073.11 | transcript | ENST00000641686.2 | protein_coding | 3/11 | chr4 | 127948479 | |||||||
| chr4:127948485 | T | A | 1 | a0001c0001t0001g0315 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.198+1319A>T | MFSD8 | ENSG00000164073.11 | transcript | ENST00000641686.2 | protein_coding | 3/11 | chr4 | 127948485 | |||||||
| chr4:127948521 | A | G | 1 | a0001c0001t0001g0298 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.198+1283T>C | MFSD8 | ENSG00000164073.11 | transcript | ENST00000641686.2 | protein_coding | 3/11 | chr4 | 127948521 | |||||||
| chr4:127948632 | G | A | 1 | a0002c0002t0002g0082 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.198+1172C>T | MFSD8 | ENSG00000164073.11 | transcript | ENST00000641686.2 | protein_coding | 3/11 | chr4 | 127948632 | |||||||
| chr4:127948888 | G | A | 1 | a0002c0002t0012g0317 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.198+916C>T | MFSD8 | ENSG00000164073.11 | transcript | ENST00000641686.2 | protein_coding | 3/11 | chr4 | 127948888 | |||||||
| chr4:127948918 | A | G | 2 | a0001c0001t0001g0260 a0001c0001t0001g0267 |
2 | HG02572.hp2 HG02723.hp2 |
intron_variant | MODIFIER | c.198+886T>C | MFSD8 | ENSG00000164073.11 | transcript | ENST00000641686.2 | protein_coding | 3/11 | chr4 | 127948918 | |||||||
| chr4:127948923 | C | T | 1 | a0003c0003t0001g0148 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.198+881G>A | MFSD8 | ENSG00000164073.11 | transcript | ENST00000641686.2 | protein_coding | 3/11 | chr4 | 127948923 | |||||||
| chr4:127949257 | A | C | 2 | a0002c0002t0005g0312 a0002c0002t0005g0313 |
2 | HG02055.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.198+547T>G | MFSD8 | ENSG00000164073.11 | transcript | ENST00000641686.2 | protein_coding | 3/11 | chr4 | 127949257 | |||||||
| chr4:127949264 | A | G | 5 | a0002c0002t0005g0312 a0002c0002t0005g0313 a0002c0002t0005g0314 others(2): Show |
6 | HG01496.hp1 HG02055.hp2 HG02572.hp1 others(3): Show |
intron_variant | MODIFIER | c.198+540T>C | MFSD8 | ENSG00000164073.11 | transcript | ENST00000641686.2 | protein_coding | 3/11 | chr4 | 127949264 | |||||||
| chr4:127949321 | A | T | 1 | a0001c0001t0001g0108 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.198+483T>A | MFSD8 | ENSG00000164073.11 | transcript | ENST00000641686.2 | protein_coding | 3/11 | chr4 | 127949321 | |||||||
| chr4:127949383 | T | C | 1 | a0001c0001t0001g0108 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.198+421A>G | MFSD8 | ENSG00000164073.11 | transcript | ENST00000641686.2 | protein_coding | 3/11 | chr4 | 127949383 | |||||||
| chr4:127949446 | T | C | 1 | a0001c0001t0001g0291 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.198+358A>G | MFSD8 | ENSG00000164073.11 | transcript | ENST00000641686.2 | protein_coding | 3/11 | chr4 | 127949446 | |||||||
| chr4:127949761 | A | C | 1 | a0002c0002t0012g0317 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.198+43T>G | MFSD8 | ENSG00000164073.11 | transcript | ENST00000641686.2 | protein_coding | 3/11 | chr4 | 127949761 | |||||||
| chr4:127949768 | T | C | 4 | a0002c0002t0006g0089 a0002c0002t0006g0090 a0002c0002t0006g0091 others(1): Show |
4 | HG01891.hp2 HG02486.hp2 HG02622.hp2 others(1): Show |
intron_variant | MODIFIER | c.198+36A>G | MFSD8 | ENSG00000164073.11 | transcript | ENST00000641686.2 | protein_coding | 3/11 | chr4 | 127949768 | |||||||
| chr4:127949881 | T | A | 4 | a0002c0002t0006g0089 a0002c0002t0006g0090 a0002c0002t0006g0091 others(1): Show |
4 | HG01891.hp2 HG02486.hp2 HG02622.hp2 others(1): Show |
intron_variant | MODIFIER | c.155-34A>T | MFSD8 | ENSG00000164073.11 | transcript | ENST00000641686.2 | protein_coding | 2/11 | chr4 | 127949881 | |||||||
| chr4:127950021 | T | C | 2 | a0001c0001t0001g0021 a0001c0001t0001g0294 |
3 | HG01516.hp2 HG01517.hp1 HG02698.hp2 |
intron_variant | MODIFIER | c.155-174A>G | MFSD8 | ENSG00000164073.11 | transcript | ENST00000641686.2 | protein_coding | 2/11 | chr4 | 127950021 | |||||||
| chr4:127950064 | C | T | 4 | a0002c0002t0006g0089 a0002c0002t0006g0090 a0002c0002t0006g0091 others(1): Show |
4 | HG01891.hp2 HG02486.hp2 HG02622.hp2 others(1): Show |
intron_variant | MODIFIER | c.155-217G>A | MFSD8 | ENSG00000164073.11 | transcript | ENST00000641686.2 | protein_coding | 2/11 | chr4 | 127950064 | |||||||
| chr4:127950071 | G | A | 2 | a0001c0001t0001g0265 a0001c0001t0001g0277 |
2 | NA18947.hp2 NA19091.hp1 |
intron_variant | MODIFIER | c.155-224C>T | MFSD8 | ENSG00000164073.11 | transcript | ENST00000641686.2 | protein_coding | 2/11 | chr4 | 127950071 | |||||||
| chr4:127950147 | A | G | 64 | a0002c0002t0002g0004 a0002c0002t0002g0008 a0002c0002t0002g0009 others(61): Show |
70 | HG00423.hp2 HG00438.hp2 HG00544.hp1 others(67): Show |
intron_variant | MODIFIER | c.155-300T>C | MFSD8 | ENSG00000164073.11 | transcript | ENST00000641686.2 | protein_coding | 2/11 | chr4 | 127950147 | |||||||
| chr4:127950154 | A | G | 64 | a0002c0002t0002g0004 a0002c0002t0002g0008 a0002c0002t0002g0009 others(61): Show |
70 | HG00423.hp2 HG00438.hp2 HG00544.hp1 others(67): Show |
intron_variant | MODIFIER | c.155-307T>C | MFSD8 | ENSG00000164073.11 | transcript | ENST00000641686.2 | protein_coding | 2/11 | chr4 | 127950154 | |||||||
| chr4:127950494 | G | A | 1 | a0001c0001t0001g0218 | 1 | HG02897.hp2 | intron_variant | MODIFIER | c.155-647C>T | MFSD8 | ENSG00000164073.11 | transcript | ENST00000641686.2 | protein_coding | 2/11 | chr4 | 127950494 | |||||||
| chr4:127950692 | CA | C | 16 | a0002c0002t0003g0093 a0002c0002t0003g0094 a0002c0002t0003g0095 others(13): Show |
16 | HG01891.hp2 HG02109.hp1 HG02257.hp2 others(13): Show |
intron_variant | MODIFIER | c.155-846delT | MFSD8 | ENSG00000164073.11 | transcript | ENST00000641686.2 | protein_coding | 2/11 | chr4 | 127950692 | |||||||
| chr4:127950818 | A | T | 4 | a0002c0002t0006g0089 a0002c0002t0006g0090 a0002c0002t0006g0091 others(1): Show |
4 | HG01891.hp2 HG02486.hp2 HG02622.hp2 others(1): Show |
intron_variant | MODIFIER | c.155-971T>A | MFSD8 | ENSG00000164073.11 | transcript | ENST00000641686.2 | protein_coding | 2/11 | chr4 | 127950818 | |||||||
| chr4:127950998 | T | C | 64 | a0002c0002t0002g0004 a0002c0002t0002g0008 a0002c0002t0002g0009 others(61): Show |
70 | HG00423.hp2 HG00438.hp2 HG00544.hp1 others(67): Show |
intron_variant | MODIFIER | c.155-1151A>G | MFSD8 | ENSG00000164073.11 | transcript | ENST00000641686.2 | protein_coding | 2/11 | chr4 | 127950998 | |||||||
| chr4:127951068 | A | G | 1 | a0002c0002t0002g0076 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.155-1221T>C | MFSD8 | ENSG00000164073.11 | transcript | ENST00000641686.2 | protein_coding | 2/11 | chr4 | 127951068 | |||||||
| chr4:127951070 | G | A | 1 | a0002c0002t0002g0076 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.155-1223C>T | MFSD8 | ENSG00000164073.11 | transcript | ENST00000641686.2 | protein_coding | 2/11 | chr4 | 127951070 | |||||||
| chr4:127951162 | G | A | 64 | a0002c0002t0002g0004 a0002c0002t0002g0008 a0002c0002t0002g0009 others(61): Show |
70 | HG00423.hp2 HG00438.hp2 HG00544.hp1 others(67): Show |
intron_variant | MODIFIER | c.155-1315C>T | MFSD8 | ENSG00000164073.11 | transcript | ENST00000641686.2 | protein_coding | 2/11 | chr4 | 127951162 | |||||||
| chr4:127951455 | C | T | 11 | a0002c0002t0003g0093 a0002c0002t0003g0094 a0002c0002t0003g0095 others(8): Show |
11 | HG02109.hp1 HG02257.hp2 HG02451.hp2 others(8): Show |
intron_variant | MODIFIER | c.155-1608G>A | MFSD8 | ENSG00000164073.11 | transcript | ENST00000641686.2 | protein_coding | 2/11 | chr4 | 127951455 | |||||||
| chr4:127951526 | C | G | 4 | a0001c0001t0001g0012 a0001c0001t0001g0111 a0001c0001t0001g0118 others(1): Show |
5 | HG02647.hp1 HG02922.hp1 HG02965.hp2 others(2): Show |
intron_variant | MODIFIER | c.155-1679G>C | MFSD8 | ENSG00000164073.11 | transcript | ENST00000641686.2 | protein_coding | 2/11 | chr4 | 127951526 | |||||||
| chr4:127951526 | C | T | 1 | a0001c0001t0001g0285 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.155-1679G>A | MFSD8 | ENSG00000164073.11 | transcript | ENST00000641686.2 | protein_coding | 2/11 | chr4 | 127951526 | |||||||
| chr4:127951550 | A | G | 1 | a0001c0001t0001g0147 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.155-1703T>C | MFSD8 | ENSG00000164073.11 | transcript | ENST00000641686.2 | protein_coding | 2/11 | chr4 | 127951550 | |||||||
| chr4:127951730 | A | AT | 9 | a0001c0001t0001g0284 a0002c0002t0002g0032 a0002c0002t0002g0037 others(6): Show |
9 | HG00609.hp2 HG02055.hp2 HG02976.hp1 others(6): Show |
intron_variant | MODIFIER | c.155-1884dupA | MFSD8 | ENSG00000164073.11 | transcript | ENST00000641686.2 | protein_coding | 2/11 | chr4 | 127951730 | |||||||
| chr4:127951730 | AT | A | 15 | a0001c0001t0001g0189 a0001c0001t0001g0266 a0002c0002t0003g0093 others(12): Show |
15 | HG00558.hp2 HG01106.hp1 HG02109.hp1 others(12): Show |
intron_variant | MODIFIER | c.155-1884delA | MFSD8 | ENSG00000164073.11 | transcript | ENST00000641686.2 | protein_coding | 2/11 | chr4 | 127951730 | |||||||
| chr4:127951797 | C | T | 1 | a0002c0002t0003g0096 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.155-1950G>A | MFSD8 | ENSG00000164073.11 | transcript | ENST00000641686.2 | protein_coding | 2/11 | chr4 | 127951797 | |||||||
| chr4:127951844 | TCA | T | 11 | a0002c0002t0003g0093 a0002c0002t0003g0094 a0002c0002t0003g0095 others(8): Show |
11 | HG02109.hp1 HG02257.hp2 HG02451.hp2 others(8): Show |
intron_variant | MODIFIER | c.155-1999_155-1998d others(4): Show |
MFSD8 | ENSG00000164073.11 | transcript | ENST00000641686.2 | protein_coding | 2/11 | chr4 | 127951844 | |||||||
| chr4:127951973 | C | T | 11 | a0002c0002t0003g0093 a0002c0002t0003g0094 a0002c0002t0003g0095 others(8): Show |
11 | HG02109.hp1 HG02257.hp2 HG02451.hp2 others(8): Show |
intron_variant | MODIFIER | c.155-2126G>A | MFSD8 | ENSG00000164073.11 | transcript | ENST00000641686.2 | protein_coding | 2/11 | chr4 | 127951973 | |||||||
| chr4:127952133 | C | T | 1 | a0002c0002t0012g0317 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.155-2286G>A | MFSD8 | ENSG00000164073.11 | transcript | ENST00000641686.2 | protein_coding | 2/11 | chr4 | 127952133 | |||||||
| chr4:127952142 | A | T | 1 | a0001c0001t0008g0242 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.155-2295T>A | MFSD8 | ENSG00000164073.11 | transcript | ENST00000641686.2 | protein_coding | 2/11 | chr4 | 127952142 | |||||||
| chr4:127952143 | T | G | 1 | a0001c0001t0008g0242 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.155-2296A>C | MFSD8 | ENSG00000164073.11 | transcript | ENST00000641686.2 | protein_coding | 2/11 | chr4 | 127952143 | |||||||
| chr4:127952144 | G | C | 1 | a0001c0001t0008g0242 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.155-2297C>G | MFSD8 | ENSG00000164073.11 | transcript | ENST00000641686.2 | protein_coding | 2/11 | chr4 | 127952144 | |||||||
| chr4:127952201 | C | G | 5 | a0002c0002t0005g0312 a0002c0002t0005g0313 a0002c0002t0005g0314 others(2): Show |
6 | HG01496.hp1 HG02055.hp2 HG02572.hp1 others(3): Show |
intron_variant | MODIFIER | c.155-2354G>C | MFSD8 | ENSG00000164073.11 | transcript | ENST00000641686.2 | protein_coding | 2/11 | chr4 | 127952201 | |||||||
| chr4:127952216 | T | C | 2 | a0002c0002t0002g0032 a0002c0002t0002g0071 |
2 | NA18977.hp1 NA19011.hp1 |
intron_variant | MODIFIER | c.155-2369A>G | MFSD8 | ENSG00000164073.11 | transcript | ENST00000641686.2 | protein_coding | 2/11 | chr4 | 127952216 | |||||||
| chr4:127952302 | G | A | 64 | a0002c0002t0002g0004 a0002c0002t0002g0008 a0002c0002t0002g0009 others(61): Show |
70 | HG00423.hp2 HG00438.hp2 HG00544.hp1 others(67): Show |
intron_variant | MODIFIER | c.155-2455C>T | MFSD8 | ENSG00000164073.11 | transcript | ENST00000641686.2 | protein_coding | 2/11 | chr4 | 127952302 | |||||||
| chr4:127952336 | G | A | 4 | a0002c0002t0006g0089 a0002c0002t0006g0090 a0002c0002t0006g0091 others(1): Show |
4 | HG01891.hp2 HG02486.hp2 HG02622.hp2 others(1): Show |
intron_variant | MODIFIER | c.155-2489C>T | MFSD8 | ENSG00000164073.11 | transcript | ENST00000641686.2 | protein_coding | 2/11 | chr4 | 127952336 | |||||||
| chr4:127952360 | C | A | 3 | a0002c0002t0005g0312 a0002c0002t0005g0313 a0002c0002t0005g0314 |
3 | HG02055.hp2 HG02976.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.155-2513G>T | MFSD8 | ENSG00000164073.11 | transcript | ENST00000641686.2 | protein_coding | 2/11 | chr4 | 127952360 | |||||||
| chr4:127952522 | G | A | 3 | a0002c0002t0005g0312 a0002c0002t0005g0313 a0002c0002t0005g0314 |
3 | HG02055.hp2 HG02976.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.155-2675C>T | MFSD8 | ENSG00000164073.11 | transcript | ENST00000641686.2 | protein_coding | 2/11 | chr4 | 127952522 | |||||||
| chr4:127952766 | A | C | 1 | a0001c0001t0001g0146 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.155-2919T>G | MFSD8 | ENSG00000164073.11 | transcript | ENST00000641686.2 | protein_coding | 2/11 | chr4 | 127952766 | |||||||
| chr4:127952783 | T | C | 3 | a0002c0002t0002g0054 a0002c0002t0002g0074 a0002c0002t0002g0077 |
3 | HG00621.hp2 NA18966.hp1 NA18978.hp2 |
intron_variant | MODIFIER | c.155-2936A>G | MFSD8 | ENSG00000164073.11 | transcript | ENST00000641686.2 | protein_coding | 2/11 | chr4 | 127952783 | |||||||
| chr4:127952869 | C | CA | 21 | a0001c0001t0001g0143 a0001c0001t0001g0202 a0001c0001t0001g0205 others(18): Show |
21 | HG00609.hp2 HG00621.hp2 HG01106.hp2 others(18): Show |
intron_variant | MODIFIER | c.155-3023dupT | MFSD8 | ENSG00000164073.11 | transcript | ENST00000641686.2 | protein_coding | 2/11 | chr4 | 127952869 | |||||||
| chr4:127952869 | CA | C | 24 | a0001c0001t0001g0113 a0001c0001t0001g0145 a0001c0001t0001g0223 others(21): Show |
24 | HG01256.hp2 HG01891.hp2 HG02109.hp1 others(21): Show |
intron_variant | MODIFIER | c.155-3023delT | MFSD8 | ENSG00000164073.11 | transcript | ENST00000641686.2 | protein_coding | 2/11 | chr4 | 127952869 | |||||||
| chr4:127952948 | A | C | 1 | a0001c0001t0001g0258 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.155-3101T>G | MFSD8 | ENSG00000164073.11 | transcript | ENST00000641686.2 | protein_coding | 2/11 | chr4 | 127952948 | |||||||
| chr4:127953133 | C | T | 1 | a0001c0001t0001g0257 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.155-3286G>A | MFSD8 | ENSG00000164073.11 | transcript | ENST00000641686.2 | protein_coding | 2/11 | chr4 | 127953133 | |||||||
| chr4:127953171 | C | A | 22 | a0001c0001t0001g0002 a0001c0001t0001g0214 a0001c0001t0001g0215 others(19): Show |
27 | HG00408.hp2 HG00597.hp1 HG02015.hp1 others(24): Show |
intron_variant | MODIFIER | c.155-3324G>T | MFSD8 | ENSG00000164073.11 | transcript | ENST00000641686.2 | protein_coding | 2/11 | chr4 | 127953171 | |||||||
| chr4:127953245 | T | C | 1 | a0001c0001t0001g0198 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.155-3398A>G | MFSD8 | ENSG00000164073.11 | transcript | ENST00000641686.2 | protein_coding | 2/11 | chr4 | 127953245 | |||||||
| chr4:127953264 | G | A | 11 | a0002c0002t0003g0093 a0002c0002t0003g0094 a0002c0002t0003g0095 others(8): Show |
11 | HG02109.hp1 HG02257.hp2 HG02451.hp2 others(8): Show |
intron_variant | MODIFIER | c.155-3417C>T | MFSD8 | ENSG00000164073.11 | transcript | ENST00000641686.2 | protein_coding | 2/11 | chr4 | 127953264 | |||||||
| chr4:127953331 | A | G | 3 | a0001c0001t0001g0234 a0001c0001t0001g0247 a0001c0001t0001g0282 |
3 | NA18956.hp1 NA18959.hp2 NA19005.hp2 |
intron_variant | MODIFIER | c.155-3484T>C | MFSD8 | ENSG00000164073.11 | transcript | ENST00000641686.2 | protein_coding | 2/11 | chr4 | 127953331 | |||||||
| chr4:127953386 | G | C | 1 | a0001c0001t0001g0202 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.155-3539C>G | MFSD8 | ENSG00000164073.11 | transcript | ENST00000641686.2 | protein_coding | 2/11 | chr4 | 127953386 | |||||||
| chr4:127953461 | C | CA | 31 | a0001c0001t0001g0144 a0001c0001t0001g0198 a0001c0001t0001g0207 others(28): Show |
33 | HG00741.hp2 HG01257.hp1 HG01257.hp2 others(30): Show |
intron_variant | MODIFIER | c.155-3615dupT | MFSD8 | ENSG00000164073.11 | transcript | ENST00000641686.2 | protein_coding | 2/11 | chr4 | 127953461 | |||||||
| chr4:127953461 | C | CAA | 61 | a0002c0002t0002g0004 a0002c0002t0002g0008 a0002c0002t0002g0009 others(58): Show |
67 | HG00423.hp2 HG00438.hp2 HG00544.hp1 others(64): Show |
intron_variant | MODIFIER | c.155-3616_155-3615d others(4): Show |
MFSD8 | ENSG00000164073.11 | transcript | ENST00000641686.2 | protein_coding | 2/11 | chr4 | 127953461 | |||||||
| chr4:127953543 | G | GT | 70 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0012 others(67): Show |
76 | HG00140.hp1 HG00140.hp2 HG00423.hp1 others(73): Show |
intron_variant | MODIFIER | c.155-3697dupA | MFSD8 | ENSG00000164073.11 | transcript | ENST00000641686.2 | protein_coding | 2/11 | chr4 | 127953543 | |||||||
| chr4:127953543 | G | GTT | 6 | a0001c0001t0001g0110 a0001c0001t0001g0198 a0001c0001t0001g0246 others(3): Show |
6 | HG00741.hp2 HG01433.hp2 HG02451.hp1 others(3): Show |
intron_variant | MODIFIER | c.155-3698_155-3697d others(4): Show |
MFSD8 | ENSG00000164073.11 | transcript | ENST00000641686.2 | protein_coding | 2/11 | chr4 | 127953543 | |||||||
| chr4:127953543 | GT | G | 35 | a0001c0001t0001g0119 a0001c0001t0001g0179 a0001c0001t0001g0277 others(32): Show |
37 | HG00423.hp2 HG00438.hp2 HG00558.hp2 others(34): Show |
intron_variant | MODIFIER | c.155-3697delA | MFSD8 | ENSG00000164073.11 | transcript | ENST00000641686.2 | protein_coding | 2/11 | chr4 | 127953543 | |||||||
| chr4:127953543 | GTT | G | 43 | a0002c0002t0002g0004 a0002c0002t0002g0009 a0002c0002t0002g0010 others(40): Show |
48 | HG00544.hp1 HG00621.hp2 HG00738.hp1 others(45): Show |
intron_variant | MODIFIER | c.155-3698_155-3697d others(4): Show |
MFSD8 | ENSG00000164073.11 | transcript | ENST00000641686.2 | protein_coding | 2/11 | chr4 | 127953543 | |||||||
| chr4:127953543 | GTTTTTTT others(5): Show |
G | 1 | a0001c0001t0001g0186 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.155-3708_155-3697d others(14): Show |
MFSD8 | ENSG00000164073.11 | transcript | ENST00000641686.2 | protein_coding | 2/11 | chr4 | 127953543 | |||||||
| chr4:127953554 | T | G | 10 | a0001c0001t0001g0017 a0001c0001t0001g0117 a0001c0001t0001g0180 others(7): Show |
11 | HG02015.hp2 HG02155.hp2 NA18946.hp2 others(8): Show |
intron_variant | MODIFIER | c.155-3707A>C | MFSD8 | ENSG00000164073.11 | transcript | ENST00000641686.2 | protein_coding | 2/11 | chr4 | 127953554 | |||||||
| chr4:127953556 | T | G | 3 | a0001c0001t0001g0241 a0001c0001t0001g0278 a0001c0001t0001g0279 |
3 | HG01256.hp1 HG01258.hp1 NA20752.hp1 |
intron_variant | MODIFIER | c.155-3709A>C | MFSD8 | ENSG00000164073.11 | transcript | ENST00000641686.2 | protein_coding | 2/11 | chr4 | 127953556 | |||||||
| chr4:127953584 | T | C | 82 | a0002c0002t0002g0004 a0002c0002t0002g0008 a0002c0002t0002g0009 others(79): Show |
89 | HG00423.hp2 HG00438.hp2 HG00544.hp1 others(86): Show |
intron_variant | MODIFIER | c.155-3737A>G | MFSD8 | ENSG00000164073.11 | transcript | ENST00000641686.2 | protein_coding | 2/11 | chr4 | 127953584 | |||||||
| chr4:127953719 | G | A | 2 | a0001c0001t0001g0118 a0001c0001t0001g0119 |
2 | HG02922.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.154+3782C>T | MFSD8 | ENSG00000164073.11 | transcript | ENST00000641686.2 | protein_coding | 2/11 | chr4 | 127953719 | |||||||
| chr4:127953901 | T | C | 1 | a0001c0001t0001g0219 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.154+3600A>G | MFSD8 | ENSG00000164073.11 | transcript | ENST00000641686.2 | protein_coding | 2/11 | chr4 | 127953901 | |||||||
| chr4:127954099 | C | T | 1 | a0001c0001t0001g0245 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.154+3402G>A | MFSD8 | ENSG00000164073.11 | transcript | ENST00000641686.2 | protein_coding | 2/11 | chr4 | 127954099 | |||||||
| chr4:127954152 | A | G | 4 | a0002c0002t0006g0089 a0002c0002t0006g0090 a0002c0002t0006g0091 others(1): Show |
4 | HG01891.hp2 HG02486.hp2 HG02622.hp2 others(1): Show |
intron_variant | MODIFIER | c.154+3349T>C | MFSD8 | ENSG00000164073.11 | transcript | ENST00000641686.2 | protein_coding | 2/11 | chr4 | 127954152 | |||||||
| chr4:127954233 | A | G | 3 | a0001c0001t0008g0242 a0001c0001t0008g0243 a0001c0001t0008g0244 |
3 | NA18949.hp2 NA19062.hp2 NA19075.hp2 |
intron_variant | MODIFIER | c.154+3268T>C | MFSD8 | ENSG00000164073.11 | transcript | ENST00000641686.2 | protein_coding | 2/11 | chr4 | 127954233 | |||||||
| chr4:127954312 | T | TC | 16 | a0002c0002t0003g0093 a0002c0002t0003g0094 a0002c0002t0003g0095 others(13): Show |
16 | HG01891.hp2 HG02109.hp1 HG02257.hp2 others(13): Show |
intron_variant | MODIFIER | c.154+3188_154+3189i others(3): Show |
MFSD8 | ENSG00000164073.11 | transcript | ENST00000641686.2 | protein_coding | 2/11 | chr4 | 127954312 | |||||||
| chr4:127954387 | A | T | 9 | a0001c0001t0001g0013 a0001c0001t0001g0109 a0001c0001t0001g0123 others(6): Show |
10 | HG01433.hp1 HG01943.hp1 HG01952.hp1 others(7): Show |
intron_variant | MODIFIER | c.154+3114T>A | MFSD8 | ENSG00000164073.11 | transcript | ENST00000641686.2 | protein_coding | 2/11 | chr4 | 127954387 | |||||||
| chr4:127954533 | T | C | 1 | a0006c0006t0001g0303 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.154+2968A>G | MFSD8 | ENSG00000164073.11 | transcript | ENST00000641686.2 | protein_coding | 2/11 | chr4 | 127954533 | |||||||
| chr4:127955357 | A | G | 1 | a0002c0002t0012g0317 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.154+2144T>C | MFSD8 | ENSG00000164073.11 | transcript | ENST00000641686.2 | protein_coding | 2/11 | chr4 | 127955357 | |||||||
| chr4:127955418 | G | A | 1 | a0001c0001t0001g0280 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.154+2083C>T | MFSD8 | ENSG00000164073.11 | transcript | ENST00000641686.2 | protein_coding | 2/11 | chr4 | 127955418 | |||||||
| chr4:127955539 | C | CA | 21 | a0001c0001t0001g0221 a0001c0001t0001g0281 a0001c0001t0001g0282 others(18): Show |
21 | HG01891.hp2 HG02109.hp1 HG02257.hp2 others(18): Show |
intron_variant | MODIFIER | c.154+1961dupT | MFSD8 | ENSG00000164073.11 | transcript | ENST00000641686.2 | protein_coding | 2/11 | chr4 | 127955539 | |||||||
| chr4:127955539 | C | CAAAA | 54 | a0002c0002t0002g0004 a0002c0002t0002g0008 a0002c0002t0002g0009 others(51): Show |
60 | HG00423.hp2 HG00438.hp2 HG00544.hp1 others(57): Show |
intron_variant | MODIFIER | c.154+1958_154+1961d others(6): Show |
MFSD8 | ENSG00000164073.11 | transcript | ENST00000641686.2 | protein_coding | 2/11 | chr4 | 127955539 | |||||||
| chr4:127955539 | C | CAAAAA | 8 | a0002c0002t0002g0036 a0002c0002t0002g0072 a0002c0002t0002g0073 others(5): Show |
8 | HG00621.hp2 HG01978.hp2 NA18956.hp2 others(5): Show |
intron_variant | MODIFIER | c.154+1957_154+1961d others(7): Show |
MFSD8 | ENSG00000164073.11 | transcript | ENST00000641686.2 | protein_coding | 2/11 | chr4 | 127955539 | |||||||
| chr4:127955539 | CA | C | 128 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(125): Show |
143 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(140): Show |
intron_variant | MODIFIER | c.154+1961delT | MFSD8 | ENSG00000164073.11 | transcript | ENST00000641686.2 | protein_coding | 2/11 | chr4 | 127955539 | |||||||
| chr4:127955539 | CAA | C | 7 | a0001c0001t0001g0022 a0001c0001t0001g0105 a0001c0001t0001g0125 others(4): Show |
8 | HG01168.hp1 HG01168.hp2 HG02273.hp1 others(5): Show |
intron_variant | MODIFIER | c.154+1960_154+1961d others(4): Show |
MFSD8 | ENSG00000164073.11 | transcript | ENST00000641686.2 | protein_coding | 2/11 | chr4 | 127955539 | |||||||
| chr4:127955625 | T | C | 1 | a0002c0002t0002g0078 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.154+1876A>G | MFSD8 | ENSG00000164073.11 | transcript | ENST00000641686.2 | protein_coding | 2/11 | chr4 | 127955625 | |||||||
| chr4:127955645 | C | G | 7 | a0001c0001t0001g0222 a0001c0001t0001g0223 a0001c0001t0001g0224 others(4): Show |
7 | HG00735.hp1 HG02615.hp2 HG02723.hp1 others(4): Show |
intron_variant | MODIFIER | c.154+1856G>C | MFSD8 | ENSG00000164073.11 | transcript | ENST00000641686.2 | protein_coding | 2/11 | chr4 | 127955645 | |||||||
| chr4:127955652 | T | C | 1 | a0001c0001t0001g0284 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.154+1849A>G | MFSD8 | ENSG00000164073.11 | transcript | ENST00000641686.2 | protein_coding | 2/11 | chr4 | 127955652 | |||||||
| chr4:127955681 | C | T | 11 | a0002c0002t0003g0093 a0002c0002t0003g0094 a0002c0002t0003g0095 others(8): Show |
11 | HG02109.hp1 HG02257.hp2 HG02451.hp2 others(8): Show |
intron_variant | MODIFIER | c.154+1820G>A | MFSD8 | ENSG00000164073.11 | transcript | ENST00000641686.2 | protein_coding | 2/11 | chr4 | 127955681 | |||||||
| chr4:127955845 | G | A | 1 | a0001c0001t0001g0285 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.154+1656C>T | MFSD8 | ENSG00000164073.11 | transcript | ENST00000641686.2 | protein_coding | 2/11 | chr4 | 127955845 | |||||||
| chr4:127955898 | C | T | 1 | a0001c0001t0001g0221 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.154+1603G>A | MFSD8 | ENSG00000164073.11 | transcript | ENST00000641686.2 | protein_coding | 2/11 | chr4 | 127955898 | |||||||
| chr4:127955962 | C | T | 4 | a0002c0002t0006g0089 a0002c0002t0006g0090 a0002c0002t0006g0091 others(1): Show |
4 | HG01891.hp2 HG02486.hp2 HG02622.hp2 others(1): Show |
intron_variant | MODIFIER | c.154+1539G>A | MFSD8 | ENSG00000164073.11 | transcript | ENST00000641686.2 | protein_coding | 2/11 | chr4 | 127955962 | |||||||
| chr4:127956095 | G | A | 1 | a0002c0002t0005g0313 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.154+1406C>T | MFSD8 | ENSG00000164073.11 | transcript | ENST00000641686.2 | protein_coding | 2/11 | chr4 | 127956095 | |||||||
| chr4:127956418 | C | A | 2 | a0001c0001t0001g0105 a0001c0001t0001g0192 |
2 | HG02523.hp1 NA18945.hp2 |
intron_variant | MODIFIER | c.154+1083G>T | MFSD8 | ENSG00000164073.11 | transcript | ENST00000641686.2 | protein_coding | 2/11 | chr4 | 127956418 | |||||||
| chr4:127956500 | G | GA | 7 | a0001c0001t0001g0193 a0002c0002t0002g0079 a0002c0002t0005g0312 others(4): Show |
7 | HG00609.hp1 HG02055.hp2 HG02486.hp1 others(4): Show |
intron_variant | MODIFIER | c.154+1000dupT | MFSD8 | ENSG00000164073.11 | transcript | ENST00000641686.2 | protein_coding | 2/11 | chr4 | 127956500 | |||||||
| chr4:127956547 | G | C | 1 | a0001c0001t0001g0288 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.154+954C>G | MFSD8 | ENSG00000164073.11 | transcript | ENST00000641686.2 | protein_coding | 2/11 | chr4 | 127956547 | |||||||
| chr4:127956711 | G | C | 64 | a0002c0002t0002g0004 a0002c0002t0002g0008 a0002c0002t0002g0009 others(61): Show |
70 | HG00423.hp2 HG00438.hp2 HG00544.hp1 others(67): Show |
intron_variant | MODIFIER | c.154+790C>G | MFSD8 | ENSG00000164073.11 | transcript | ENST00000641686.2 | protein_coding | 2/11 | chr4 | 127956711 | |||||||
| chr4:127956818 | C | CA | 23 | a0001c0001t0001g0194 a0001c0001t0001g0286 a0001c0001t0001g0287 others(20): Show |
24 | HG00609.hp1 HG01496.hp1 HG02055.hp2 others(21): Show |
intron_variant | MODIFIER | c.154+682dupT | MFSD8 | ENSG00000164073.11 | transcript | ENST00000641686.2 | protein_coding | 2/11 | chr4 | 127956818 | |||||||
| chr4:127956818 | C | CAA | 56 | a0002c0002t0002g0004 a0002c0002t0002g0008 a0002c0002t0002g0009 others(53): Show |
62 | HG00423.hp2 HG00438.hp2 HG00544.hp1 others(59): Show |
intron_variant | MODIFIER | c.154+681_154+682dup others(2): Show |
MFSD8 | ENSG00000164073.11 | transcript | ENST00000641686.2 | protein_coding | 2/11 | chr4 | 127956818 | |||||||
| chr4:127956860 | A | G | 4 | a0002c0002t0006g0089 a0002c0002t0006g0090 a0002c0002t0006g0091 others(1): Show |
4 | HG01891.hp2 HG02486.hp2 HG02622.hp2 others(1): Show |
intron_variant | MODIFIER | c.154+641T>C | MFSD8 | ENSG00000164073.11 | transcript | ENST00000641686.2 | protein_coding | 2/11 | chr4 | 127956860 | |||||||
| chr4:127956980 | C | G | 1 | a0001c0001t0001g0124 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.154+521G>C | MFSD8 | ENSG00000164073.11 | transcript | ENST00000641686.2 | protein_coding | 2/11 | chr4 | 127956980 | |||||||
| chr4:127956994 | T | C | 1 | a0001c0001t0001g0304 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.154+507A>G | MFSD8 | ENSG00000164073.11 | transcript | ENST00000641686.2 | protein_coding | 2/11 | chr4 | 127956994 | |||||||
| chr4:127957026 | T | C | 1 | a0001c0001t0001g0289 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.154+475A>G | MFSD8 | ENSG00000164073.11 | transcript | ENST00000641686.2 | protein_coding | 2/11 | chr4 | 127957026 | |||||||
| chr4:127957188 | T | C | 1 | a0002c0002t0002g0080 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.154+313A>G | MFSD8 | ENSG00000164073.11 | transcript | ENST00000641686.2 | protein_coding | 2/11 | chr4 | 127957188 | |||||||
| chr4:127957243 | G | A | 11 | a0002c0002t0003g0093 a0002c0002t0003g0094 a0002c0002t0003g0095 others(8): Show |
11 | HG02109.hp1 HG02257.hp2 HG02451.hp2 others(8): Show |
intron_variant | MODIFIER | c.154+258C>T | MFSD8 | ENSG00000164073.11 | transcript | ENST00000641686.2 | protein_coding | 2/11 | chr4 | 127957243 | |||||||
| chr4:127957275 | T | C | 1 | a0001c0001t0018g0196 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.154+226A>G | MFSD8 | ENSG00000164073.11 | transcript | ENST00000641686.2 | protein_coding | 2/11 | chr4 | 127957275 | |||||||
| chr4:127957325 | C | T | 4 | a0002c0002t0006g0089 a0002c0002t0006g0090 a0002c0002t0006g0091 others(1): Show |
4 | HG01891.hp2 HG02486.hp2 HG02622.hp2 others(1): Show |
intron_variant | MODIFIER | c.154+176G>A | MFSD8 | ENSG00000164073.11 | transcript | ENST00000641686.2 | protein_coding | 2/11 | chr4 | 127957325 | |||||||
| chr4:127957386 | G | A | 4 | a0002c0002t0006g0089 a0002c0002t0006g0090 a0002c0002t0006g0091 others(1): Show |
4 | HG01891.hp2 HG02486.hp2 HG02622.hp2 others(1): Show |
intron_variant | MODIFIER | c.154+115C>T | MFSD8 | ENSG00000164073.11 | transcript | ENST00000641686.2 | protein_coding | 2/11 | chr4 | 127957386 | |||||||
| chr4:127957865 | A | G | 1 | a0001c0001t0001g0220 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.63-273T>C | MFSD8 | ENSG00000164073.11 | transcript | ENST00000641686.2 | protein_coding | 1/11 | chr4 | 127957865 | |||||||
| chr4:127957918 | C | T | 4 | a0002c0002t0006g0089 a0002c0002t0006g0090 a0002c0002t0006g0091 others(1): Show |
4 | HG01891.hp2 HG02486.hp2 HG02622.hp2 others(1): Show |
intron_variant | MODIFIER | c.63-326G>A | MFSD8 | ENSG00000164073.11 | transcript | ENST00000641686.2 | protein_coding | 1/11 | chr4 | 127957918 | |||||||
| chr4:127957967 | C | T | 1 | a0001c0001t0001g0219 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.63-375G>A | MFSD8 | ENSG00000164073.11 | transcript | ENST00000641686.2 | protein_coding | 1/11 | chr4 | 127957967 | |||||||
| chr4:127958011 | A | G | 3 | a0002c0002t0005g0312 a0002c0002t0005g0313 a0002c0002t0005g0314 |
3 | HG02055.hp2 HG02976.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.63-419T>C | MFSD8 | ENSG00000164073.11 | transcript | ENST00000641686.2 | protein_coding | 1/11 | chr4 | 127958011 | |||||||
| chr4:127958065 | A | G | 64 | a0002c0002t0002g0004 a0002c0002t0002g0008 a0002c0002t0002g0009 others(61): Show |
70 | HG00423.hp2 HG00438.hp2 HG00544.hp1 others(67): Show |
intron_variant | MODIFIER | c.63-473T>C | MFSD8 | ENSG00000164073.11 | transcript | ENST00000641686.2 | protein_coding | 1/11 | chr4 | 127958065 | |||||||
| chr4:127958133 | A | C | 1 | a0001c0001t0001g0108 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.63-541T>G | MFSD8 | ENSG00000164073.11 | transcript | ENST00000641686.2 | protein_coding | 1/11 | chr4 | 127958133 | |||||||
| chr4:127958239 | C | T | 1 | a0001c0001t0001g0108 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.63-647G>A | MFSD8 | ENSG00000164073.11 | transcript | ENST00000641686.2 | protein_coding | 1/11 | chr4 | 127958239 | |||||||
| chr4:127958375 | C | G | 4 | a0002c0002t0006g0089 a0002c0002t0006g0090 a0002c0002t0006g0091 others(1): Show |
4 | HG01891.hp2 HG02486.hp2 HG02622.hp2 others(1): Show |
intron_variant | MODIFIER | c.63-783G>C | MFSD8 | ENSG00000164073.11 | transcript | ENST00000641686.2 | protein_coding | 1/11 | chr4 | 127958375 | |||||||
| chr4:127958672 | C | T | 3 | a0002c0002t0005g0312 a0002c0002t0005g0313 a0002c0002t0005g0314 |
3 | HG02055.hp2 HG02976.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.63-1080G>A | MFSD8 | ENSG00000164073.11 | transcript | ENST00000641686.2 | protein_coding | 1/11 | chr4 | 127958672 | |||||||
| chr4:127958680 | T | C | 11 | a0002c0002t0003g0093 a0002c0002t0003g0094 a0002c0002t0003g0095 others(8): Show |
11 | HG02109.hp1 HG02257.hp2 HG02451.hp2 others(8): Show |
intron_variant | MODIFIER | c.63-1088A>G | MFSD8 | ENSG00000164073.11 | transcript | ENST00000641686.2 | protein_coding | 1/11 | chr4 | 127958680 | |||||||
| chr4:127958839 | G | A | 11 | a0002c0002t0003g0093 a0002c0002t0003g0094 a0002c0002t0003g0095 others(8): Show |
11 | HG02109.hp1 HG02257.hp2 HG02451.hp2 others(8): Show |
intron_variant | MODIFIER | c.63-1247C>T | MFSD8 | ENSG00000164073.11 | transcript | ENST00000641686.2 | protein_coding | 1/11 | chr4 | 127958839 | |||||||
| chr4:127958849 | A | G | 1 | a0002c0002t0023g0030 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.63-1257T>C | MFSD8 | ENSG00000164073.11 | transcript | ENST00000641686.2 | protein_coding | 1/11 | chr4 | 127958849 | |||||||
| chr4:127958959 | G | T | 11 | a0002c0002t0003g0093 a0002c0002t0003g0094 a0002c0002t0003g0095 others(8): Show |
11 | HG02109.hp1 HG02257.hp2 HG02451.hp2 others(8): Show |
intron_variant | MODIFIER | c.63-1367C>A | MFSD8 | ENSG00000164073.11 | transcript | ENST00000641686.2 | protein_coding | 1/11 | chr4 | 127958959 | |||||||
| chr4:127959030 | T | C | 8 | a0001c0001t0001g0021 a0001c0001t0001g0290 a0001c0001t0001g0291 others(5): Show |
9 | HG00735.hp2 HG01074.hp1 HG01175.hp1 others(6): Show |
intron_variant | MODIFIER | c.63-1438A>G | MFSD8 | ENSG00000164073.11 | transcript | ENST00000641686.2 | protein_coding | 1/11 | chr4 | 127959030 | |||||||
| chr4:127959139 | G | A | 1 | a0003c0003t0001g0197 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.63-1547C>T | MFSD8 | ENSG00000164073.11 | transcript | ENST00000641686.2 | protein_coding | 1/11 | chr4 | 127959139 | |||||||
| chr4:127959203 | T | C | 5 | a0001c0001t0001g0022 a0001c0001t0001g0307 a0001c0001t0001g0308 others(2): Show |
6 | HG01168.hp2 HG02280.hp2 HG02451.hp1 others(3): Show |
intron_variant | MODIFIER | c.63-1611A>G | MFSD8 | ENSG00000164073.11 | transcript | ENST00000641686.2 | protein_coding | 1/11 | chr4 | 127959203 | |||||||
| chr4:127959276 | T | C | 11 | a0002c0002t0003g0093 a0002c0002t0003g0094 a0002c0002t0003g0095 others(8): Show |
11 | HG02109.hp1 HG02257.hp2 HG02451.hp2 others(8): Show |
intron_variant | MODIFIER | c.63-1684A>G | MFSD8 | ENSG00000164073.11 | transcript | ENST00000641686.2 | protein_coding | 1/11 | chr4 | 127959276 | |||||||
| chr4:127959347 | A | C | 1 | a0001c0001t0001g0123 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.63-1755T>G | MFSD8 | ENSG00000164073.11 | transcript | ENST00000641686.2 | protein_coding | 1/11 | chr4 | 127959347 | |||||||
| chr4:127959526 | A | G | 4 | a0002c0002t0006g0089 a0002c0002t0006g0090 a0002c0002t0006g0091 others(1): Show |
4 | HG01891.hp2 HG02486.hp2 HG02622.hp2 others(1): Show |
intron_variant | MODIFIER | c.63-1934T>C | MFSD8 | ENSG00000164073.11 | transcript | ENST00000641686.2 | protein_coding | 1/11 | chr4 | 127959526 | |||||||
| chr4:127959699 | T | C | 1 | a0001c0001t0001g0297 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.63-2107A>G | MFSD8 | ENSG00000164073.11 | transcript | ENST00000641686.2 | protein_coding | 1/11 | chr4 | 127959699 | |||||||
| chr4:127959879 | A | G | 64 | a0002c0002t0002g0004 a0002c0002t0002g0008 a0002c0002t0002g0009 others(61): Show |
70 | HG00423.hp2 HG00438.hp2 HG00544.hp1 others(67): Show |
intron_variant | MODIFIER | c.63-2287T>C | MFSD8 | ENSG00000164073.11 | transcript | ENST00000641686.2 | protein_coding | 1/11 | chr4 | 127959879 | |||||||
| chr4:127959968 | G | A | 11 | a0002c0002t0003g0093 a0002c0002t0003g0094 a0002c0002t0003g0095 others(8): Show |
11 | HG02109.hp1 HG02257.hp2 HG02451.hp2 others(8): Show |
intron_variant | MODIFIER | c.63-2376C>T | MFSD8 | ENSG00000164073.11 | transcript | ENST00000641686.2 | protein_coding | 1/11 | chr4 | 127959968 | |||||||
| chr4:127959974 | A | C | 11 | a0002c0002t0003g0093 a0002c0002t0003g0094 a0002c0002t0003g0095 others(8): Show |
11 | HG02109.hp1 HG02257.hp2 HG02451.hp2 others(8): Show |
intron_variant | MODIFIER | c.63-2382T>G | MFSD8 | ENSG00000164073.11 | transcript | ENST00000641686.2 | protein_coding | 1/11 | chr4 | 127959974 | |||||||
| chr4:127960149 | T | C | 4 | a0002c0002t0006g0089 a0002c0002t0006g0090 a0002c0002t0006g0091 others(1): Show |
4 | HG01891.hp2 HG02486.hp2 HG02622.hp2 others(1): Show |
intron_variant | MODIFIER | c.63-2557A>G | MFSD8 | ENSG00000164073.11 | transcript | ENST00000641686.2 | protein_coding | 1/11 | chr4 | 127960149 | |||||||
| chr4:127960246 | C | T | 3 | a0002c0002t0005g0312 a0002c0002t0005g0313 a0002c0002t0005g0314 |
3 | HG02055.hp2 HG02976.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.63-2654G>A | MFSD8 | ENSG00000164073.11 | transcript | ENST00000641686.2 | protein_coding | 1/11 | chr4 | 127960246 | |||||||
| chr4:127960391 | G | A | 64 | a0002c0002t0002g0004 a0002c0002t0002g0008 a0002c0002t0002g0009 others(61): Show |
70 | HG00423.hp2 HG00438.hp2 HG00544.hp1 others(67): Show |
intron_variant | MODIFIER | c.63-2799C>T | MFSD8 | ENSG00000164073.11 | transcript | ENST00000641686.2 | protein_coding | 1/11 | chr4 | 127960391 | |||||||
| chr4:127960438 | G | A | 1 | a0001c0001t0001g0012 | 2 | HG02647.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.63-2846C>T | MFSD8 | ENSG00000164073.11 | transcript | ENST00000641686.2 | protein_coding | 1/11 | chr4 | 127960438 | |||||||
| chr4:127960447 | T | C | 5 | a0001c0001t0001g0022 a0001c0001t0001g0307 a0001c0001t0001g0308 others(2): Show |
6 | HG01168.hp2 HG02280.hp2 HG02451.hp1 others(3): Show |
intron_variant | MODIFIER | c.63-2855A>G | MFSD8 | ENSG00000164073.11 | transcript | ENST00000641686.2 | protein_coding | 1/11 | chr4 | 127960447 | |||||||
| chr4:127960508 | C | A | 11 | a0002c0002t0003g0093 a0002c0002t0003g0094 a0002c0002t0003g0095 others(8): Show |
11 | HG02109.hp1 HG02257.hp2 HG02451.hp2 others(8): Show |
intron_variant | MODIFIER | c.63-2916G>T | MFSD8 | ENSG00000164073.11 | transcript | ENST00000641686.2 | protein_coding | 1/11 | chr4 | 127960508 | |||||||
| chr4:127960529 | A | AAAAT | 64 | a0002c0002t0002g0004 a0002c0002t0002g0008 a0002c0002t0002g0009 others(61): Show |
70 | HG00423.hp2 HG00438.hp2 HG00544.hp1 others(67): Show |
intron_variant | MODIFIER | c.63-2941_63-2938dup others(4): Show |
MFSD8 | ENSG00000164073.11 | transcript | ENST00000641686.2 | protein_coding | 1/11 | chr4 | 127960529 | |||||||
| chr4:127960592 | A | T | 3 | a0001c0001t0001g0106 a0001c0001t0001g0107 a0001c0001t0001g0122 |
3 | HG03486.hp2 NA19240.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.63-3000T>A | MFSD8 | ENSG00000164073.11 | transcript | ENST00000641686.2 | protein_coding | 1/11 | chr4 | 127960592 | |||||||
| chr4:127960654 | A | G | 2 | a0004c0004t0005g0092 a0004c0004t0010g0011 |
3 | HG01496.hp1 HG02572.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.63-3062T>C | MFSD8 | ENSG00000164073.11 | transcript | ENST00000641686.2 | protein_coding | 1/11 | chr4 | 127960654 | |||||||
| chr4:127960748 | A | C | 11 | a0002c0002t0003g0093 a0002c0002t0003g0094 a0002c0002t0003g0095 others(8): Show |
11 | HG02109.hp1 HG02257.hp2 HG02451.hp2 others(8): Show |
intron_variant | MODIFIER | c.63-3156T>G | MFSD8 | ENSG00000164073.11 | transcript | ENST00000641686.2 | protein_coding | 1/11 | chr4 | 127960748 | |||||||
| chr4:127960761 | A | G | 4 | a0002c0002t0006g0089 a0002c0002t0006g0090 a0002c0002t0006g0091 others(1): Show |
4 | HG01891.hp2 HG02486.hp2 HG02622.hp2 others(1): Show |
intron_variant | MODIFIER | c.63-3169T>C | MFSD8 | ENSG00000164073.11 | transcript | ENST00000641686.2 | protein_coding | 1/11 | chr4 | 127960761 | |||||||
| chr4:127960957 | C | T | 1 | a0001c0001t0001g0218 | 1 | HG02897.hp2 | intron_variant | MODIFIER | c.63-3365G>A | MFSD8 | ENSG00000164073.11 | transcript | ENST00000641686.2 | protein_coding | 1/11 | chr4 | 127960957 | |||||||
| chr4:127960970 | C | G | 3 | a0002c0002t0005g0312 a0002c0002t0005g0313 a0002c0002t0005g0314 |
3 | HG02055.hp2 HG02976.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.63-3378G>C | MFSD8 | ENSG00000164073.11 | transcript | ENST00000641686.2 | protein_coding | 1/11 | chr4 | 127960970 | |||||||
| chr4:127961039 | G | T | 1 | a0001c0001t0001g0024 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.63-3447C>A | MFSD8 | ENSG00000164073.11 | transcript | ENST00000641686.2 | protein_coding | 1/11 | chr4 | 127961039 | |||||||
| chr4:127961047 | T | A | 1 | a0002c0002t0012g0317 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.63-3455A>T | MFSD8 | ENSG00000164073.11 | transcript | ENST00000641686.2 | protein_coding | 1/11 | chr4 | 127961047 | |||||||
| chr4:127961090 | A | C | 4 | a0002c0002t0006g0089 a0002c0002t0006g0090 a0002c0002t0006g0091 others(1): Show |
4 | HG01891.hp2 HG02486.hp2 HG02622.hp2 others(1): Show |
intron_variant | MODIFIER | c.63-3498T>G | MFSD8 | ENSG00000164073.11 | transcript | ENST00000641686.2 | protein_coding | 1/11 | chr4 | 127961090 | |||||||
| chr4:127961240 | T | TTG | 85 | a0002c0002t0002g0004 a0002c0002t0002g0008 a0002c0002t0002g0009 others(82): Show |
92 | HG00423.hp2 HG00438.hp2 HG00544.hp1 others(89): Show |
intron_variant | MODIFIER | c.63-3650_63-3649dup others(2): Show |
MFSD8 | ENSG00000164073.11 | transcript | ENST00000641686.2 | protein_coding | 1/11 | chr4 | 127961240 | |||||||
| chr4:127961263 | T | C | 1 | a0001c0001t0001g0305 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.63-3671A>G | MFSD8 | ENSG00000164073.11 | transcript | ENST00000641686.2 | protein_coding | 1/11 | chr4 | 127961263 | |||||||
| chr4:127961535 | C | T | 2 | a0001c0001t0011g0216 a0001c0001t0011g0217 |
2 | NA18987.hp2 NA18998.hp1 |
intron_variant | MODIFIER | c.62+3537G>A | MFSD8 | ENSG00000164073.11 | transcript | ENST00000641686.2 | protein_coding | 1/11 | chr4 | 127961535 | |||||||
| chr4:127961699 | C | G | 1 | a0002c0002t0012g0317 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.62+3373G>C | MFSD8 | ENSG00000164073.11 | transcript | ENST00000641686.2 | protein_coding | 1/11 | chr4 | 127961699 | |||||||
| chr4:127961775 | T | C | 85 | a0002c0002t0002g0004 a0002c0002t0002g0008 a0002c0002t0002g0009 others(82): Show |
92 | HG00423.hp2 HG00438.hp2 HG00544.hp1 others(89): Show |
intron_variant | MODIFIER | c.62+3297A>G | MFSD8 | ENSG00000164073.11 | transcript | ENST00000641686.2 | protein_coding | 1/11 | chr4 | 127961775 | |||||||
| chr4:127961787 | C | G | 3 | a0002c0002t0005g0312 a0002c0002t0005g0313 a0002c0002t0005g0314 |
3 | HG02055.hp2 HG02976.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.62+3285G>C | MFSD8 | ENSG00000164073.11 | transcript | ENST00000641686.2 | protein_coding | 1/11 | chr4 | 127961787 | |||||||
| chr4:127961797 | G | T | 3 | a0002c0002t0005g0312 a0002c0002t0005g0313 a0002c0002t0005g0314 |
3 | HG02055.hp2 HG02976.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.62+3275C>A | MFSD8 | ENSG00000164073.11 | transcript | ENST00000641686.2 | protein_coding | 1/11 | chr4 | 127961797 | |||||||
| chr4:127961820 | C | CA | 113 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(110): Show |
128 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(125): Show |
intron_variant | MODIFIER | c.62+3251dupT | MFSD8 | ENSG00000164073.11 | transcript | ENST00000641686.2 | protein_coding | 1/11 | chr4 | 127961820 | |||||||
| chr4:127961820 | C | CAA | 9 | a0001c0001t0001g0198 a0001c0001t0001g0199 a0001c0001t0001g0201 others(6): Show |
9 | HG00408.hp1 HG00544.hp2 HG00741.hp2 others(6): Show |
intron_variant | MODIFIER | c.62+3250_62+3251dup others(2): Show |
MFSD8 | ENSG00000164073.11 | transcript | ENST00000641686.2 | protein_coding | 1/11 | chr4 | 127961820 | |||||||
| chr4:127961820 | C | CAAAA | 8 | a0002c0002t0003g0096 a0002c0002t0003g0097 a0002c0002t0003g0098 others(5): Show |
8 | HG02109.hp1 HG02630.hp2 HG02809.hp1 others(5): Show |
intron_variant | MODIFIER | c.62+3248_62+3251dup others(4): Show |
MFSD8 | ENSG00000164073.11 | transcript | ENST00000641686.2 | protein_coding | 1/11 | chr4 | 127961820 | |||||||
| chr4:127961853 | T | C | 4 | a0002c0002t0002g0085 a0002c0002t0002g0086 a0002c0002t0002g0087 others(1): Show |
4 | NA18952.hp1 NA19007.hp1 NA19056.hp1 others(1): Show |
intron_variant | MODIFIER | c.62+3219A>G | MFSD8 | ENSG00000164073.11 | transcript | ENST00000641686.2 | protein_coding | 1/11 | chr4 | 127961853 | |||||||
| chr4:127962156 | A | T | 1 | a0001c0001t0001g0105 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.62+2916T>A | MFSD8 | ENSG00000164073.11 | transcript | ENST00000641686.2 | protein_coding | 1/11 | chr4 | 127962156 | |||||||
| chr4:127962321 | G | A | 11 | a0002c0002t0003g0093 a0002c0002t0003g0094 a0002c0002t0003g0095 others(8): Show |
11 | HG02109.hp1 HG02257.hp2 HG02451.hp2 others(8): Show |
intron_variant | MODIFIER | c.62+2751C>T | MFSD8 | ENSG00000164073.11 | transcript | ENST00000641686.2 | protein_coding | 1/11 | chr4 | 127962321 | |||||||
| chr4:127962498 | G | T | 1 | a0001c0001t0001g0307 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.62+2574C>A | MFSD8 | ENSG00000164073.11 | transcript | ENST00000641686.2 | protein_coding | 1/11 | chr4 | 127962498 | |||||||
| chr4:127962719 | A | G | 1 | a0001c0001t0001g0215 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.62+2353T>C | MFSD8 | ENSG00000164073.11 | transcript | ENST00000641686.2 | protein_coding | 1/11 | chr4 | 127962719 | |||||||
| chr4:127962771 | A | G | 1 | a0002c0002t0012g0317 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.62+2301T>C | MFSD8 | ENSG00000164073.11 | transcript | ENST00000641686.2 | protein_coding | 1/11 | chr4 | 127962771 | |||||||
| chr4:127962804 | A | G | 2 | a0001c0001t0001g0214 a0008c0008t0001g0213 |
2 | HG02083.hp1 NA19090.hp1 |
intron_variant | MODIFIER | c.62+2268T>C | MFSD8 | ENSG00000164073.11 | transcript | ENST00000641686.2 | protein_coding | 1/11 | chr4 | 127962804 | |||||||
| chr4:127962892 | G | C | 11 | a0002c0002t0003g0093 a0002c0002t0003g0094 a0002c0002t0003g0095 others(8): Show |
11 | HG02109.hp1 HG02257.hp2 HG02451.hp2 others(8): Show |
intron_variant | MODIFIER | c.62+2180C>G | MFSD8 | ENSG00000164073.11 | transcript | ENST00000641686.2 | protein_coding | 1/11 | chr4 | 127962892 | |||||||
| chr4:127963022 | A | G | 64 | a0002c0002t0002g0004 a0002c0002t0002g0008 a0002c0002t0002g0009 others(61): Show |
70 | HG00423.hp2 HG00438.hp2 HG00544.hp1 others(67): Show |
intron_variant | MODIFIER | c.62+2050T>C | MFSD8 | ENSG00000164073.11 | transcript | ENST00000641686.2 | protein_coding | 1/11 | chr4 | 127963022 | |||||||
| chr4:127963115 | A | G | 1 | a0002c0002t0002g0029 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.62+1957T>C | MFSD8 | ENSG00000164073.11 | transcript | ENST00000641686.2 | protein_coding | 1/11 | chr4 | 127963115 | |||||||
| chr4:127963170 | T | C | 2 | a0001c0001t0001g0207 a0001c0001t0001g0208 |
2 | HG01257.hp2 HG01258.hp2 |
intron_variant | MODIFIER | c.62+1902A>G | MFSD8 | ENSG00000164073.11 | transcript | ENST00000641686.2 | protein_coding | 1/11 | chr4 | 127963170 | |||||||
| chr4:127963182 | A | C | 2 | a0001c0005t0001g0103 a0001c0005t0001g0104 |
2 | HG02735.hp1 HG03017.hp2 |
intron_variant | MODIFIER | c.62+1890T>G | MFSD8 | ENSG00000164073.11 | transcript | ENST00000641686.2 | protein_coding | 1/11 | chr4 | 127963182 | |||||||
| chr4:127963194 | C | G | 1 | a0001c0001t0001g0212 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.62+1878G>C | MFSD8 | ENSG00000164073.11 | transcript | ENST00000641686.2 | protein_coding | 1/11 | chr4 | 127963194 | |||||||
| chr4:127963267 | A | C | 3 | a0001c0001t0001g0209 a0001c0001t0001g0210 a0001c0001t0001g0211 |
3 | HG01884.hp1 HG02055.hp1 HG02647.hp2 |
intron_variant | MODIFIER | c.62+1805T>G | MFSD8 | ENSG00000164073.11 | transcript | ENST00000641686.2 | protein_coding | 1/11 | chr4 | 127963267 | |||||||
| chr4:127963286 | T | G | 85 | a0002c0002t0002g0004 a0002c0002t0002g0008 a0002c0002t0002g0009 others(82): Show |
92 | HG00423.hp2 HG00438.hp2 HG00544.hp1 others(89): Show |
intron_variant | MODIFIER | c.62+1786A>C | MFSD8 | ENSG00000164073.11 | transcript | ENST00000641686.2 | protein_coding | 1/11 | chr4 | 127963286 | |||||||
| chr4:127963288 | T | C | 5 | a0001c0001t0001g0022 a0001c0001t0001g0307 a0001c0001t0001g0308 others(2): Show |
6 | HG01168.hp2 HG02280.hp2 HG02451.hp1 others(3): Show |
intron_variant | MODIFIER | c.62+1784A>G | MFSD8 | ENSG00000164073.11 | transcript | ENST00000641686.2 | protein_coding | 1/11 | chr4 | 127963288 | |||||||
| chr4:127963455 | A | C | 118 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0006 others(115): Show |
133 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(130): Show |
intron_variant | MODIFIER | c.62+1617T>G | MFSD8 | ENSG00000164073.11 | transcript | ENST00000641686.2 | protein_coding | 1/11 | chr4 | 127963455 | |||||||
| chr4:127963698 | A | G | 85 | a0002c0002t0002g0004 a0002c0002t0002g0008 a0002c0002t0002g0009 others(82): Show |
92 | HG00423.hp2 HG00438.hp2 HG00544.hp1 others(89): Show |
intron_variant | MODIFIER | c.62+1374T>C | MFSD8 | ENSG00000164073.11 | transcript | ENST00000641686.2 | protein_coding | 1/11 | chr4 | 127963698 | |||||||
| chr4:127963886 | T | C | 1 | a0002c0002t0006g0306 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.62+1186A>G | MFSD8 | ENSG00000164073.11 | transcript | ENST00000641686.2 | protein_coding | 1/11 | chr4 | 127963886 | |||||||
| chr4:127963988 | C | G | 3 | a0001c0001t0007g0007 a0001c0001t0007g0027 a0001c0001t0007g0028 |
4 | NA18950.hp2 NA18973.hp2 NA18977.hp2 others(1): Show |
intron_variant | MODIFIER | c.62+1084G>C | MFSD8 | ENSG00000164073.11 | transcript | ENST00000641686.2 | protein_coding | 1/11 | chr4 | 127963988 | |||||||
| chr4:127963990 | G | C | 1 | a0001c0009t0014g0310 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.62+1082C>G | MFSD8 | ENSG00000164073.11 | transcript | ENST00000641686.2 | protein_coding | 1/11 | chr4 | 127963990 | |||||||
| chr4:127964011 | C | T | 3 | a0001c0001t0001g0024 a0001c0001t0001g0025 a0001c0001t0001g0026 |
3 | HG00673.hp2 HG02155.hp1 NA18747.hp1 |
intron_variant | MODIFIER | c.62+1061G>A | MFSD8 | ENSG00000164073.11 | transcript | ENST00000641686.2 | protein_coding | 1/11 | chr4 | 127964011 | |||||||
| chr4:127964191 | C | A | 5 | a0001c0001t0001g0022 a0001c0001t0001g0307 a0001c0001t0001g0308 others(2): Show |
6 | HG01168.hp2 HG02280.hp2 HG02451.hp1 others(3): Show |
intron_variant | MODIFIER | c.62+881G>T | MFSD8 | ENSG00000164073.11 | transcript | ENST00000641686.2 | protein_coding | 1/11 | chr4 | 127964191 | |||||||
| chr4:127964214 | G | T | 1 | a0002c0002t0012g0317 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.62+858C>A | MFSD8 | ENSG00000164073.11 | transcript | ENST00000641686.2 | protein_coding | 1/11 | chr4 | 127964214 | |||||||
| chr4:127964485 | A | G | 1 | a0001c0001t0001g0023 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.62+587T>C | MFSD8 | ENSG00000164073.11 | transcript | ENST00000641686.2 | protein_coding | 1/11 | chr4 | 127964485 | |||||||
| chr4:127964541 | C | A | 1 | a0001c0001t0001g0311 | 1 | NA18980.hp2 | intron_variant | MODIFIER | c.62+531G>T | MFSD8 | ENSG00000164073.11 | transcript | ENST00000641686.2 | protein_coding | 1/11 | chr4 | 127964541 | |||||||
| chr4:127964561 | G | A | 3 | a0002c0002t0005g0312 a0002c0002t0005g0313 a0002c0002t0005g0314 |
3 | HG02055.hp2 HG02976.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.62+511C>T | MFSD8 | ENSG00000164073.11 | transcript | ENST00000641686.2 | protein_coding | 1/11 | chr4 | 127964561 | |||||||
| chr4:127964728 | G | A | 1 | a0001c0001t0001g0315 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.62+344C>T | MFSD8 | ENSG00000164073.11 | transcript | ENST00000641686.2 | protein_coding | 1/11 | chr4 | 127964728 | |||||||
| chr4:127964790 | T | C | 1 | a0002c0002t0003g0316 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.62+282A>G | MFSD8 | ENSG00000164073.11 | transcript | ENST00000641686.2 | protein_coding | 1/11 | chr4 | 127964790 | |||||||
| chr4:127964792 | T | C | 1 | a0002c0002t0012g0317 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.62+280A>G | MFSD8 | ENSG00000164073.11 | transcript | ENST00000641686.2 | protein_coding | 1/11 | chr4 | 127964792 |