Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| geneid | 84641 |
|---|---|
| ensemblid | ENSG00000148110.17 |
| hgncid | 23376 |
| symbol | MFSD14B |
| name | major facilitator superfamily domain containing 14B |
| refseq_nuc | NM_032558.3 |
| refseq_prot | NP_115947.2 |
| ensembl_nuc | ENST00000375344.8 |
| ensembl_prot | ENSP00000364493.3 |
| mane_status | MANE Select |
| chr | chr9 |
| start | 94374569 |
| end | 94461042 |
| strand | + |
| ver | v1.2 |
| region | chr9:94374569-94461042 |
| region5000 | chr9:94369569-94466042 |
| regionname0 | MFSD14B_chr9_94374569_94461042 |
| regionname5000 | MFSD14B_chr9_94369569_94466042 |
| ahapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 506 | 349 | 78 | 69 | 144 | 16 | 40 | 106 | MFSD14B_chr9_94369569_94466042 | MFSD14B | copy fasta | chr9 | 94369569 | 94466042 |
| a0002 | 0/0 | 506 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | MFSD14B_chr9_94369569_94466042 | MFSD14B | copy fasta | chr9 | 94369569 | 94466042 |
| chapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| c0001 | 1/1 | 1521 | 340 | 77 | 66 | 144 | 15 | 36 | MFSD14B_chr9_94369569_94466042 | MFSD14B | copy fasta | chr9 | 94369569 | 94466042 |
| c0002 | 0/0 | 1521 | 8 | 0 | 3 | 0 | 1 | 4 | MFSD14B_chr9_94369569_94466042 | MFSD14B | copy fasta | chr9 | 94369569 | 94466042 |
| c0003 | 0/0 | 1521 | 1 | 1 | 0 | 0 | 0 | 0 | MFSD14B_chr9_94369569_94466042 | MFSD14B | copy fasta | chr9 | 94369569 | 94466042 |
| c0004 | 0/0 | 1521 | 1 | 0 | 1 | 0 | 0 | 0 | MFSD14B_chr9_94369569_94466042 | MFSD14B | copy fasta | chr9 | 94369569 | 94466042 |
| thapid | grch38chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| t0001 | 0/0 | 1880 | 111 | 15 | 30 | 49 | 4 | 13 | MFSD14B_chr9_94369569_94466042 | MFSD14B | copy fasta | chr9 | 94369569 | 94466042 |
| t0002 | 0/0 | 1881 | 64 | 18 | 5 | 36 | 4 | 1 | MFSD14B_chr9_94369569_94466042 | MFSD14B | copy fasta | chr9 | 94369569 | 94466042 |
| t0003 | 1/0 | 1882 | 64 | 3 | 12 | 33 | 5 | 10 | MFSD14B_chr9_94369569_94466042 | MFSD14B | copy fasta | chr9 | 94369569 | 94466042 |
| t0004 | 0/0 | 1881 | 36 | 6 | 6 | 16 | 0 | 8 | MFSD14B_chr9_94369569_94466042 | MFSD14B | copy fasta | chr9 | 94369569 | 94466042 |
| t0005 | 0/0 | 1877 | 13 | 8 | 5 | 0 | 0 | 0 | MFSD14B_chr9_94369569_94466042 | MFSD14B | copy fasta | chr9 | 94369569 | 94466042 |
| t0006 | 0/0 | 1881 | 11 | 10 | 1 | 0 | 0 | 0 | MFSD14B_chr9_94369569_94466042 | MFSD14B | copy fasta | chr9 | 94369569 | 94466042 |
| t0007 | 0/0 | 1880 | 11 | 7 | 2 | 1 | 0 | 1 | MFSD14B_chr9_94369569_94466042 | MFSD14B | copy fasta | chr9 | 94369569 | 94466042 |
| t0008 | 0/0 | 1880 | 10 | 9 | 1 | 0 | 0 | 0 | MFSD14B_chr9_94369569_94466042 | MFSD14B | copy fasta | chr9 | 94369569 | 94466042 |
| t0009 | 0/0 | 1880 | 7 | 0 | 3 | 0 | 1 | 3 | MFSD14B_chr9_94369569_94466042 | MFSD14B | copy fasta | chr9 | 94369569 | 94466042 |
| t0010 | 0/1 | 1882 | 4 | 0 | 2 | 0 | 0 | 1 | MFSD14B_chr9_94369569_94466042 | MFSD14B | copy fasta | chr9 | 94369569 | 94466042 |
| t0011 | 0/0 | 1881 | 3 | 0 | 1 | 1 | 1 | 0 | MFSD14B_chr9_94369569_94466042 | MFSD14B | copy fasta | chr9 | 94369569 | 94466042 |
| t0012 | 0/0 | 1882 | 3 | 0 | 0 | 3 | 0 | 0 | MFSD14B_chr9_94369569_94466042 | MFSD14B | copy fasta | chr9 | 94369569 | 94466042 |
| t0013 | 0/0 | 1879 | 2 | 0 | 0 | 2 | 0 | 0 | MFSD14B_chr9_94369569_94466042 | MFSD14B | copy fasta | chr9 | 94369569 | 94466042 |
| t0014 | 0/0 | 1879 | 2 | 0 | 0 | 1 | 1 | 0 | MFSD14B_chr9_94369569_94466042 | MFSD14B | copy fasta | chr9 | 94369569 | 94466042 |
| t0015 | 0/0 | 1869 | 1 | 0 | 0 | 0 | 0 | 1 | MFSD14B_chr9_94369569_94466042 | MFSD14B | copy fasta | chr9 | 94369569 | 94466042 |
| t0016 | 0/0 | 1880 | 1 | 1 | 0 | 0 | 0 | 0 | MFSD14B_chr9_94369569_94466042 | MFSD14B | copy fasta | chr9 | 94369569 | 94466042 |
| t0017 | 0/0 | 1879 | 1 | 1 | 0 | 0 | 0 | 0 | MFSD14B_chr9_94369569_94466042 | MFSD14B | copy fasta | chr9 | 94369569 | 94466042 |
| t0018 | 0/0 | 1881 | 1 | 0 | 0 | 0 | 0 | 1 | MFSD14B_chr9_94369569_94466042 | MFSD14B | copy fasta | chr9 | 94369569 | 94466042 |
| t0019 | 0/0 | 1880 | 1 | 0 | 1 | 0 | 0 | 0 | MFSD14B_chr9_94369569_94466042 | MFSD14B | copy fasta | chr9 | 94369569 | 94466042 |
| t0020 | 0/0 | 1881 | 1 | 0 | 1 | 0 | 0 | 0 | MFSD14B_chr9_94369569_94466042 | MFSD14B | copy fasta | chr9 | 94369569 | 94466042 |
| t0021 | 0/0 | 1881 | 1 | 0 | 0 | 0 | 0 | 1 | MFSD14B_chr9_94369569_94466042 | MFSD14B | copy fasta | chr9 | 94369569 | 94466042 |
| t0022 | 0/0 | 1882 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD14B_chr9_94369569_94466042 | MFSD14B | copy fasta | chr9 | 94369569 | 94466042 |
| t0023 | 0/0 | 1880 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD14B_chr9_94369569_94466042 | MFSD14B | copy fasta | chr9 | 94369569 | 94466042 |
| ghapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| g0001 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| g0002 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| g0003 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| g0004 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| g0005 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| g0006 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| g0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| g0015 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| g0018 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| g0021 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| g0026 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| g0028 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| g0029 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| g0039 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| g0040 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| g0041 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| g0043 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| g0044 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| g0048 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| g0051 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| g0052 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| g0054 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| g0055 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| g0056 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| g0057 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| g0058 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| g0062 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| g0065 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| g0069 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| g0070 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| g0076 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| g0077 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| g0079 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| g0080 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| g0081 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| g0083 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| g0084 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| g0085 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| g0086 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| g0087 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| g0088 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| g0089 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| g0091 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| g0092 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| g0093 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| g0094 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| g0095 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| g0097 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| g0098 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| g0103 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| g0108 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| g0121 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| g0122 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| g0127 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| g0128 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| g0133 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| g0134 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| g0135 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| g0136 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| g0146 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| g0148 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| g0152 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| g0154 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| g0157 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| g0163 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| g0168 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| g0169 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| g0170 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| g0171 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| g0176 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| g0177 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| g0178 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| g0189 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| g0190 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| g0191 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| g0202 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| g0203 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| g0204 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| g0209 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| g0210 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| g0211 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| g0212 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| g0213 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| g0214 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| g0215 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| g0216 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| g0217 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| g0221 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| g0222 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| g0225 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| g0226 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| g0228 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| g0232 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| g0233 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| g0234 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| g0235 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| g0236 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| g0237 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| g0238 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| g0239 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| g0240 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| g0241 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| g0248 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| g0265 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| g0269 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| g0276 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| g0277 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| g0278 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| g0279 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| g0281 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| g0282 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| g0285 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| g0286 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| g0287 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| g0293 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| g0294 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| g0295 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| g0296 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| g0297 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| g0299 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| g0300 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| g0302 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| g0304 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| g0305 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| g0306 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| g0307 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| g0308 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| g0309 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| g0310 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| g0311 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| g0312 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| g0313 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| g0314 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| g0315 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| g0316 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| g0317 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| g0318 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| g0319 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| g0320 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| g0321 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| g0322 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| g0323 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| g0324 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| g0325 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| g0326 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| g0327 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| g0328 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| g0329 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| g0330 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| g0331 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| g0332 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| g0333 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| g0334 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| g0335 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| g0336 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| g0337 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| g0338 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| g0339 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| g0340 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| g0341 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| g0342 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| g0343 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| g0344 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| achapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 1521 | 340 | 77 | 66 | 144 | 15 | 36 | MFSD14B_chr9_94369569_94466042 | MFSD14B | copy fasta | chr9 | 94369569 | 94466042 |
| a0001c0002 | 0/0 | 1521 | 8 | 0 | 3 | 0 | 1 | 4 | MFSD14B_chr9_94369569_94466042 | MFSD14B | copy fasta | chr9 | 94369569 | 94466042 |
| a0001c0003 | 0/0 | 1521 | 1 | 1 | 0 | 0 | 0 | 0 | MFSD14B_chr9_94369569_94466042 | MFSD14B | copy fasta | chr9 | 94369569 | 94466042 |
| a0002c0004 | 0/0 | 1521 | 1 | 0 | 1 | 0 | 0 | 0 | MFSD14B_chr9_94369569_94466042 | MFSD14B | copy fasta | chr9 | 94369569 | 94466042 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/0 | 3400 | 110 | 15 | 29 | 49 | 4 | 13 | MFSD14B_chr9_94369569_94466042 | MFSD14B | copy fasta | chr9 | 94369569 | 94466042 |
| a0001c0001t0002 | 0/0 | 3401 | 64 | 18 | 5 | 36 | 4 | 1 | MFSD14B_chr9_94369569_94466042 | MFSD14B | copy fasta | chr9 | 94369569 | 94466042 |
| a0001c0001t0003 | 1/0 | 3402 | 64 | 3 | 12 | 33 | 5 | 10 | MFSD14B_chr9_94369569_94466042 | MFSD14B | copy fasta | chr9 | 94369569 | 94466042 |
| a0001c0001t0004 | 0/0 | 3401 | 35 | 5 | 6 | 16 | 0 | 8 | MFSD14B_chr9_94369569_94466042 | MFSD14B | copy fasta | chr9 | 94369569 | 94466042 |
| a0001c0001t0005 | 0/0 | 3397 | 13 | 8 | 5 | 0 | 0 | 0 | MFSD14B_chr9_94369569_94466042 | MFSD14B | copy fasta | chr9 | 94369569 | 94466042 |
| a0001c0001t0006 | 0/0 | 3401 | 11 | 10 | 1 | 0 | 0 | 0 | MFSD14B_chr9_94369569_94466042 | MFSD14B | copy fasta | chr9 | 94369569 | 94466042 |
| a0001c0001t0007 | 0/0 | 3400 | 11 | 7 | 2 | 1 | 0 | 1 | MFSD14B_chr9_94369569_94466042 | MFSD14B | copy fasta | chr9 | 94369569 | 94466042 |
| a0001c0001t0008 | 0/0 | 3400 | 10 | 9 | 1 | 0 | 0 | 0 | MFSD14B_chr9_94369569_94466042 | MFSD14B | copy fasta | chr9 | 94369569 | 94466042 |
| a0001c0001t0010 | 0/1 | 3402 | 4 | 0 | 2 | 0 | 0 | 1 | MFSD14B_chr9_94369569_94466042 | MFSD14B | copy fasta | chr9 | 94369569 | 94466042 |
| a0001c0001t0011 | 0/0 | 3401 | 3 | 0 | 1 | 1 | 1 | 0 | MFSD14B_chr9_94369569_94466042 | MFSD14B | copy fasta | chr9 | 94369569 | 94466042 |
| a0001c0001t0012 | 0/0 | 3402 | 3 | 0 | 0 | 3 | 0 | 0 | MFSD14B_chr9_94369569_94466042 | MFSD14B | copy fasta | chr9 | 94369569 | 94466042 |
| a0001c0001t0013 | 0/0 | 3399 | 2 | 0 | 0 | 2 | 0 | 0 | MFSD14B_chr9_94369569_94466042 | MFSD14B | copy fasta | chr9 | 94369569 | 94466042 |
| a0001c0001t0014 | 0/0 | 3399 | 2 | 0 | 0 | 1 | 1 | 0 | MFSD14B_chr9_94369569_94466042 | MFSD14B | copy fasta | chr9 | 94369569 | 94466042 |
| a0001c0001t0015 | 0/0 | 3389 | 1 | 0 | 0 | 0 | 0 | 1 | MFSD14B_chr9_94369569_94466042 | MFSD14B | copy fasta | chr9 | 94369569 | 94466042 |
| a0001c0001t0016 | 0/0 | 3400 | 1 | 1 | 0 | 0 | 0 | 0 | MFSD14B_chr9_94369569_94466042 | MFSD14B | copy fasta | chr9 | 94369569 | 94466042 |
| a0001c0001t0017 | 0/0 | 3399 | 1 | 1 | 0 | 0 | 0 | 0 | MFSD14B_chr9_94369569_94466042 | MFSD14B | copy fasta | chr9 | 94369569 | 94466042 |
| a0001c0001t0018 | 0/0 | 3401 | 1 | 0 | 0 | 0 | 0 | 1 | MFSD14B_chr9_94369569_94466042 | MFSD14B | copy fasta | chr9 | 94369569 | 94466042 |
| a0001c0001t0019 | 0/0 | 3400 | 1 | 0 | 1 | 0 | 0 | 0 | MFSD14B_chr9_94369569_94466042 | MFSD14B | copy fasta | chr9 | 94369569 | 94466042 |
| a0001c0001t0020 | 0/0 | 3401 | 1 | 0 | 1 | 0 | 0 | 0 | MFSD14B_chr9_94369569_94466042 | MFSD14B | copy fasta | chr9 | 94369569 | 94466042 |
| a0001c0001t0022 | 0/0 | 3402 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD14B_chr9_94369569_94466042 | MFSD14B | copy fasta | chr9 | 94369569 | 94466042 |
| a0001c0001t0023 | 0/0 | 3400 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD14B_chr9_94369569_94466042 | MFSD14B | copy fasta | chr9 | 94369569 | 94466042 |
| a0001c0002t0009 | 0/0 | 3400 | 7 | 0 | 3 | 0 | 1 | 3 | MFSD14B_chr9_94369569_94466042 | MFSD14B | copy fasta | chr9 | 94369569 | 94466042 |
| a0001c0002t0021 | 0/0 | 3401 | 1 | 0 | 0 | 0 | 0 | 1 | MFSD14B_chr9_94369569_94466042 | MFSD14B | copy fasta | chr9 | 94369569 | 94466042 |
| a0001c0003t0004 | 0/0 | 3401 | 1 | 1 | 0 | 0 | 0 | 0 | MFSD14B_chr9_94369569_94466042 | MFSD14B | copy fasta | chr9 | 94369569 | 94466042 |
| a0002c0004t0001 | 0/0 | 3400 | 1 | 0 | 1 | 0 | 0 | 0 | MFSD14B_chr9_94369569_94466042 | MFSD14B | copy fasta | chr9 | 94369569 | 94466042 |
| actghapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| a0001c0001t0001g0003 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| a0001c0001t0001g0077 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| a0001c0001t0001g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| a0001c0001t0001g0079 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| a0001c0001t0001g0080 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| a0001c0001t0001g0081 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| a0001c0001t0001g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| a0001c0001t0001g0084 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| a0001c0001t0001g0085 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| a0001c0001t0001g0086 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| a0001c0001t0001g0087 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| a0001c0001t0001g0088 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| a0001c0001t0001g0089 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| a0001c0001t0001g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| a0001c0001t0001g0091 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| a0001c0001t0001g0092 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| a0001c0001t0001g0093 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| a0001c0001t0001g0094 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| a0001c0001t0001g0095 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| a0001c0001t0001g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| a0001c0001t0001g0097 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| a0001c0001t0001g0098 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| a0001c0001t0001g0225 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| a0001c0001t0001g0226 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| a0001c0001t0001g0228 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| a0001c0001t0001g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| a0001c0001t0001g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| a0001c0001t0001g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| a0001c0001t0001g0232 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| a0001c0001t0001g0233 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| a0001c0001t0001g0234 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| a0001c0001t0001g0235 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| a0001c0001t0001g0236 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| a0001c0001t0001g0237 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| a0001c0001t0001g0238 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| a0001c0001t0001g0239 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| a0001c0001t0001g0240 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| a0001c0001t0001g0241 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| a0001c0001t0001g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| a0001c0001t0001g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| a0001c0001t0001g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| a0001c0001t0001g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| a0001c0001t0001g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| a0001c0001t0001g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| a0001c0001t0001g0248 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| a0001c0001t0001g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| a0001c0001t0001g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| a0001c0001t0001g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| a0001c0001t0001g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| a0001c0001t0001g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| a0001c0001t0001g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| a0001c0001t0001g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| a0001c0001t0001g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| a0001c0001t0001g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| a0001c0001t0001g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| a0001c0001t0001g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| a0001c0001t0001g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| a0001c0001t0001g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| a0001c0001t0001g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| a0001c0001t0001g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| a0001c0001t0001g0265 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| a0001c0001t0001g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| a0001c0001t0001g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| a0001c0001t0001g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| a0001c0001t0001g0269 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| a0001c0001t0001g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| a0001c0001t0001g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| a0001c0001t0001g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| a0001c0001t0001g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| a0001c0001t0001g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| a0001c0001t0001g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| a0001c0001t0001g0276 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| a0001c0001t0001g0277 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| a0001c0001t0001g0278 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| a0001c0001t0001g0279 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| a0001c0001t0001g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| a0001c0001t0001g0281 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| a0001c0001t0001g0282 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| a0001c0001t0001g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| a0001c0001t0001g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| a0001c0001t0001g0285 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| a0001c0001t0001g0286 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| a0001c0001t0001g0287 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| a0001c0001t0001g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| a0001c0001t0001g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| a0001c0001t0001g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| a0001c0001t0001g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| a0001c0001t0001g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| a0001c0001t0001g0293 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| a0001c0001t0001g0294 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| a0001c0001t0001g0295 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| a0001c0001t0001g0296 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| a0001c0001t0001g0297 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| a0001c0001t0001g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| a0001c0001t0001g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| a0001c0001t0001g0302 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| a0001c0001t0001g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| a0001c0001t0001g0304 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| a0001c0001t0001g0305 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| a0001c0001t0001g0306 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| a0001c0001t0001g0307 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| a0001c0001t0001g0308 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| a0001c0001t0001g0309 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| a0001c0001t0001g0310 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| a0001c0001t0001g0311 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| a0001c0001t0001g0312 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| a0001c0001t0002g0004 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| a0001c0001t0002g0029 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| a0001c0001t0002g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| a0001c0001t0002g0039 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| a0001c0001t0002g0040 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| a0001c0001t0002g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| a0001c0001t0002g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| a0001c0001t0002g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| a0001c0001t0002g0128 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| a0001c0001t0002g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| a0001c0001t0002g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| a0001c0001t0002g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| a0001c0001t0002g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| a0001c0001t0002g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| a0001c0001t0002g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| a0001c0001t0002g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| a0001c0001t0002g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| a0001c0001t0002g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| a0001c0001t0002g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| a0001c0001t0002g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| a0001c0001t0002g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| a0001c0001t0002g0148 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| a0001c0001t0002g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| a0001c0001t0002g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| a0001c0001t0002g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| a0001c0001t0002g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| a0001c0001t0002g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| a0001c0001t0002g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| a0001c0001t0002g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| a0001c0001t0002g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| a0001c0001t0002g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| a0001c0001t0002g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| a0001c0001t0002g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| a0001c0001t0002g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| a0001c0001t0002g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| a0001c0001t0002g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| a0001c0001t0002g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| a0001c0001t0002g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| a0001c0001t0002g0315 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| a0001c0001t0002g0316 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| a0001c0001t0002g0317 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| a0001c0001t0002g0318 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| a0001c0001t0002g0319 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| a0001c0001t0002g0320 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| a0001c0001t0002g0321 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| a0001c0001t0002g0322 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| a0001c0001t0002g0323 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| a0001c0001t0002g0324 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| a0001c0001t0002g0325 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| a0001c0001t0002g0326 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| a0001c0001t0002g0327 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| a0001c0001t0002g0328 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| a0001c0001t0002g0329 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| a0001c0001t0002g0330 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| a0001c0001t0002g0331 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| a0001c0001t0002g0333 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| a0001c0001t0002g0334 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| a0001c0001t0002g0335 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| a0001c0001t0002g0339 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| a0001c0001t0002g0340 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| a0001c0001t0002g0341 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| a0001c0001t0002g0342 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| a0001c0001t0002g0343 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| a0001c0001t0003g0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| a0001c0001t0003g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| a0001c0001t0003g0076 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| a0001c0001t0003g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| a0001c0001t0003g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| a0001c0001t0003g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| a0001c0001t0003g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| a0001c0001t0003g0127 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| a0001c0001t0003g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| a0001c0001t0003g0133 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| a0001c0001t0003g0134 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| a0001c0001t0003g0135 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| a0001c0001t0003g0136 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| a0001c0001t0003g0146 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| a0001c0001t0003g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| a0001c0001t0003g0152 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| a0001c0001t0003g0154 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| a0001c0001t0003g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| a0001c0001t0003g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| a0001c0001t0003g0157 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| a0001c0001t0003g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| a0001c0001t0003g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| a0001c0001t0003g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| a0001c0001t0003g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| a0001c0001t0003g0163 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| a0001c0001t0003g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| a0001c0001t0003g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| a0001c0001t0003g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| a0001c0001t0003g0168 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| a0001c0001t0003g0169 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| a0001c0001t0003g0170 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| a0001c0001t0003g0171 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| a0001c0001t0003g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| a0001c0001t0003g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| a0001c0001t0003g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| a0001c0001t0003g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| a0001c0001t0003g0176 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| a0001c0001t0003g0177 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| a0001c0001t0003g0178 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| a0001c0001t0003g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| a0001c0001t0003g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| a0001c0001t0003g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| a0001c0001t0003g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| a0001c0001t0003g0189 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| a0001c0001t0003g0190 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| a0001c0001t0003g0191 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| a0001c0001t0003g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| a0001c0001t0003g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| a0001c0001t0003g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| a0001c0001t0003g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| a0001c0001t0003g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| a0001c0001t0003g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| a0001c0001t0003g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| a0001c0001t0003g0202 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| a0001c0001t0003g0203 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| a0001c0001t0003g0204 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| a0001c0001t0003g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| a0001c0001t0003g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| a0001c0001t0003g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| a0001c0001t0003g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| a0001c0001t0003g0217 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| a0001c0001t0003g0221 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| a0001c0001t0003g0222 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| a0001c0001t0003g0337 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| a0001c0001t0004g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| a0001c0001t0004g0028 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| a0001c0001t0004g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| a0001c0001t0004g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| a0001c0001t0004g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| a0001c0001t0004g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| a0001c0001t0004g0043 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| a0001c0001t0004g0044 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| a0001c0001t0004g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| a0001c0001t0004g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| a0001c0001t0004g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| a0001c0001t0004g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| a0001c0001t0004g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| a0001c0001t0004g0051 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| a0001c0001t0004g0052 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| a0001c0001t0004g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| a0001c0001t0004g0056 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| a0001c0001t0004g0057 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| a0001c0001t0004g0058 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| a0001c0001t0004g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| a0001c0001t0004g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| a0001c0001t0004g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| a0001c0001t0004g0062 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| a0001c0001t0004g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| a0001c0001t0004g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| a0001c0001t0004g0065 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| a0001c0001t0004g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| a0001c0001t0004g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| a0001c0001t0004g0069 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| a0001c0001t0004g0070 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| a0001c0001t0004g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| a0001c0001t0004g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| a0001c0001t0004g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| a0001c0001t0004g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| a0001c0001t0004g0313 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| a0001c0001t0005g0002 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| a0001c0001t0005g0018 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| a0001c0001t0005g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| a0001c0001t0005g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| a0001c0001t0005g0021 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| a0001c0001t0005g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| a0001c0001t0005g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| a0001c0001t0005g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| a0001c0001t0005g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| a0001c0001t0005g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| a0001c0001t0005g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| a0001c0001t0005g0314 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| a0001c0001t0006g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| a0001c0001t0006g0108 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| a0001c0001t0006g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| a0001c0001t0006g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| a0001c0001t0006g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| a0001c0001t0006g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| a0001c0001t0006g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| a0001c0001t0006g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| a0001c0001t0006g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| a0001c0001t0006g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| a0001c0001t0006g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| a0001c0001t0007g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| a0001c0001t0007g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| a0001c0001t0007g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| a0001c0001t0007g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| a0001c0001t0007g0103 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| a0001c0001t0007g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| a0001c0001t0007g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| a0001c0001t0007g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| a0001c0001t0007g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| a0001c0001t0007g0336 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| a0001c0001t0007g0338 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| a0001c0001t0008g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| a0001c0001t0008g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| a0001c0001t0008g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| a0001c0001t0008g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| a0001c0001t0008g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| a0001c0001t0008g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| a0001c0001t0008g0015 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| a0001c0001t0008g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| a0001c0001t0008g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| a0001c0001t0008g0344 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| a0001c0001t0010g0026 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| a0001c0001t0010g0048 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| a0001c0001t0010g0054 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| a0001c0001t0010g0055 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| a0001c0001t0011g0121 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| a0001c0001t0011g0122 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| a0001c0001t0011g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| a0001c0001t0012g0005 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| a0001c0001t0012g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| a0001c0001t0013g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| a0001c0001t0013g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| a0001c0001t0014g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| a0001c0001t0014g0300 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| a0001c0001t0015g0006 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| a0001c0001t0016g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| a0001c0001t0017g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| a0001c0001t0018g0041 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| a0001c0001t0019g0083 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| a0001c0001t0020g0332 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| a0001c0001t0022g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| a0001c0001t0023g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| a0001c0002t0009g0209 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| a0001c0002t0009g0210 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| a0001c0002t0009g0211 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| a0001c0002t0009g0212 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| a0001c0002t0009g0213 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| a0001c0002t0009g0214 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| a0001c0002t0009g0215 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| a0001c0002t0021g0216 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| a0001c0003t0004g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| a0002c0004t0001g0299 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0002 | g0128 | EUR | GBR | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| HG00099 | hp2 | a0001 | c0001 | t0001 | g0092 | EUR | GBR | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| HG00140 | hp1 | a0001 | c0001 | t0003 | g0176 | EUR | GBR | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| HG00140 | hp2 | a0001 | c0002 | t0009 | g0212 | EUR | GBR | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| HG00280 | hp1 | a0001 | c0001 | t0003 | g0134 | EUR | FIN | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| HG00280 | hp2 | a0001 | c0001 | t0001 | g0098 | EUR | FIN | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| HG00323 | hp1 | a0001 | c0001 | t0001 | g0077 | EUR | FIN | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| HG00323 | hp2 | a0001 | c0001 | t0014 | g0300 | EUR | FIN | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| HG00408 | hp1 | a0001 | c0001 | t0003 | g0179 | EAS | CHS | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| HG00408 | hp2 | a0001 | c0001 | t0001 | g0292 | EAS | CHS | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| HG00423 | hp1 | a0001 | c0001 | t0001 | g0251 | EAS | CHS | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| HG00423 | hp2 | a0001 | c0001 | t0001 | g0275 | EAS | CHS | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| HG00438 | hp1 | a0001 | c0001 | t0001 | g0280 | EAS | CHS | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| HG00438 | hp2 | a0001 | c0001 | t0001 | g0267 | EAS | CHS | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| HG00544 | hp1 | a0001 | c0001 | t0007 | g0223 | EAS | CHS | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| HG00544 | hp2 | a0001 | c0001 | t0002 | g0153 | EAS | CHS | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| HG00558 | hp1 | a0001 | c0001 | t0003 | g0129 | EAS | CHS | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| HG00558 | hp2 | a0001 | c0001 | t0002 | g0132 | EAS | CHS | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| HG00597 | hp1 | a0001 | c0001 | t0004 | g0072 | EAS | CHS | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| HG00597 | hp2 | a0001 | c0001 | t0003 | g0192 | EAS | CHS | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| HG00621 | hp1 | a0001 | c0001 | t0001 | g0264 | EAS | CHS | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| HG00621 | hp2 | a0001 | c0001 | t0003 | g0160 | EAS | CHS | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| HG00639 | hp1 | a0001 | c0001 | t0002 | g0322 | AMR | PUR | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| HG00639 | hp2 | a0001 | c0001 | t0004 | g0028 | AMR | PUR | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| HG00642 | hp1 | a0001 | c0001 | t0010 | g0026 | AMR | PUR | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| HG00642 | hp2 | a0001 | c0001 | t0001 | g0003 | AMR | PUR | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| HG00673 | hp1 | a0001 | c0001 | t0001 | g0266 | EAS | CHS | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| HG00673 | hp2 | a0001 | c0001 | t0003 | g0193 | EAS | CHS | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| HG00733 | hp1 | a0001 | c0001 | t0004 | g0043 | AMR | PUR | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| HG00733 | hp2 | a0001 | c0001 | t0001 | g0082 | AMR | PUR | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| HG00741 | hp1 | a0001 | c0001 | t0002 | g0148 | AMR | PUR | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| HG00741 | hp2 | a0001 | c0002 | t0009 | g0213 | AMR | PUR | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| HG01069 | hp1 | a0001 | c0001 | t0005 | g0002 | AMR | PUR | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| HG01069 | hp2 | a0001 | c0001 | t0001 | g0239 | AMR | PUR | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| HG01070 | hp1 | a0001 | c0001 | t0011 | g0121 | AMR | PUR | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| HG01070 | hp2 | a0001 | c0001 | t0004 | g0313 | AMR | PUR | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| HG01071 | hp1 | a0001 | c0001 | t0005 | g0002 | AMR | PUR | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| HG01071 | hp2 | a0001 | c0001 | t0005 | g0314 | AMR | PUR | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| HG01074 | hp1 | a0001 | c0001 | t0001 | g0096 | AMR | PUR | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| HG01074 | hp2 | a0001 | c0001 | t0003 | g0177 | AMR | PUR | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| HG01081 | hp1 | a0001 | c0001 | t0008 | g0015 | AMR | PUR | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| HG01081 | hp2 | a0001 | c0001 | t0005 | g0018 | AMR | PUR | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| HG01099 | hp1 | a0001 | c0001 | t0001 | g0226 | AMR | PUR | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| HG01099 | hp2 | a0001 | c0001 | t0004 | g0057 | AMR | PUR | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| HG01106 | hp1 | a0001 | c0001 | t0003 | g0190 | AMR | PUR | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| HG01106 | hp2 | a0001 | c0001 | t0001 | g0277 | AMR | PUR | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| HG01109 | hp1 | a0001 | c0001 | t0005 | g0021 | AMR | PUR | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| HG01109 | hp2 | a0001 | c0001 | t0002 | g0321 | AMR | PUR | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| HG01167 | hp1 | a0001 | c0001 | t0001 | g0095 | AMR | PUR | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| HG01167 | hp2 | a0001 | c0001 | t0001 | g0238 | AMR | PUR | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| HG01169 | hp1 | a0001 | c0001 | t0001 | g0089 | AMR | PUR | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| HG01169 | hp2 | a0001 | c0001 | t0003 | g0157 | AMR | PUR | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| HG01192 | hp1 | a0001 | c0001 | t0003 | g0189 | AMR | PUR | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| HG01192 | hp2 | a0001 | c0001 | t0001 | g0236 | AMR | PUR | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| HG01243 | hp1 | a0001 | c0001 | t0002 | g0029 | AMR | PUR | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| HG01243 | hp2 | a0001 | c0001 | t0006 | g0108 | AMR | PUR | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| HG01255 | hp1 | a0001 | c0001 | t0020 | g0332 | AMR | CLM | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| HG01255 | hp2 | a0001 | c0002 | t0009 | g0210 | AMR | CLM | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| HG01256 | hp1 | a0001 | c0001 | t0001 | g0232 | AMR | CLM | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| HG01256 | hp2 | a0001 | c0001 | t0007 | g0336 | AMR | CLM | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| HG01257 | hp1 | a0001 | c0001 | t0010 | g0054 | AMR | CLM | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| HG01257 | hp2 | a0001 | c0001 | t0001 | g0003 | AMR | CLM | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| HG01258 | hp1 | a0001 | c0001 | t0001 | g0234 | AMR | CLM | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| HG01258 | hp2 | a0001 | c0001 | t0001 | g0086 | AMR | CLM | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| HG01261 | hp1 | a0001 | c0001 | t0001 | g0228 | AMR | CLM | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| HG01261 | hp2 | a0001 | c0001 | t0001 | g0088 | AMR | CLM | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| HG01346 | hp1 | a0001 | c0001 | t0003 | g0222 | AMR | CLM | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| HG01346 | hp2 | a0001 | c0001 | t0001 | g0269 | AMR | CLM | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| HG01358 | hp1 | a0001 | c0001 | t0001 | g0080 | AMR | CLM | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| HG01358 | hp2 | a0001 | c0001 | t0001 | g0237 | AMR | CLM | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| HG01361 | hp1 | a0001 | c0002 | t0009 | g0214 | AMR | CLM | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| HG01361 | hp2 | a0001 | c0001 | t0019 | g0083 | AMR | CLM | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| HG01496 | hp1 | a0001 | c0001 | t0001 | g0279 | AMR | CLM | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| HG01496 | hp2 | a0001 | c0001 | t0007 | g0338 | AMR | CLM | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| HG01516 | hp1 | a0001 | c0001 | t0002 | g0039 | EUR | IBS | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| HG01516 | hp2 | a0001 | c0001 | t0003 | g0133 | EUR | IBS | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| HG01517 | hp1 | a0001 | c0001 | t0002 | g0040 | EUR | IBS | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| HG01517 | hp2 | a0001 | c0001 | t0011 | g0122 | EUR | IBS | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| HG01884 | hp1 | a0001 | c0001 | t0007 | g0101 | AFR | ACB | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| HG01884 | hp2 | a0001 | c0001 | t0002 | g0340 | AFR | ACB | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| HG01934 | hp1 | a0001 | c0001 | t0004 | g0058 | AMR | PEL | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| HG01934 | hp2 | a0001 | c0001 | t0003 | g0203 | AMR | PEL | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| HG01952 | hp1 | a0001 | c0001 | t0002 | g0316 | AMR | PEL | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| HG01952 | hp2 | a0001 | c0001 | t0003 | g0163 | AMR | PEL | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| HG01975 | hp1 | a0001 | c0001 | t0001 | g0081 | AMR | PEL | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| HG01975 | hp2 | a0001 | c0001 | t0003 | g0135 | AMR | PEL | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| HG01981 | hp1 | a0001 | c0001 | t0001 | g0240 | AMR | PEL | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| HG01981 | hp2 | a0001 | c0001 | t0001 | g0278 | AMR | PEL | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| HG02004 | hp1 | a0001 | c0001 | t0003 | g0146 | AMR | PEL | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| HG02004 | hp2 | a0001 | c0001 | t0001 | g0233 | AMR | PEL | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| HG02015 | hp1 | a0001 | c0001 | t0002 | g0343 | EAS | KHV | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| HG02015 | hp2 | a0001 | c0001 | t0001 | g0260 | EAS | KHV | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| HG02027 | hp1 | a0001 | c0001 | t0001 | g0261 | EAS | KHV | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| HG02027 | hp2 | a0001 | c0001 | t0003 | g0196 | EAS | KHV | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| HG02040 | hp1 | a0001 | c0001 | t0001 | g0284 | EAS | KHV | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| HG02040 | hp2 | a0001 | c0001 | t0013 | g0024 | EAS | KHV | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| HG02055 | hp1 | a0001 | c0001 | t0001 | g0090 | AFR | ACB | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| HG02055 | hp2 | a0001 | c0001 | t0002 | g0224 | AFR | ACB | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| HG02071 | hp1 | a0001 | c0001 | t0002 | g0141 | EAS | KHV | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| HG02071 | hp2 | a0001 | c0001 | t0004 | g0053 | EAS | KHV | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| HG02074 | hp1 | a0001 | c0001 | t0002 | g0194 | EAS | KHV | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| HG02074 | hp2 | a0001 | c0001 | t0001 | g0290 | EAS | KHV | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| HG02083 | hp1 | a0001 | c0001 | t0001 | g0289 | EAS | KHV | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| HG02083 | hp2 | a0001 | c0001 | t0002 | g0004 | EAS | KHV | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| HG02132 | hp1 | a0001 | c0001 | t0002 | g0143 | EAS | KHV | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| HG02132 | hp2 | a0001 | c0001 | t0013 | g0023 | EAS | KHV | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| HG02135 | hp1 | a0001 | c0001 | t0003 | g0197 | EAS | KHV | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| HG02135 | hp2 | a0001 | c0001 | t0023 | g0256 | EAS | KHV | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| HG02148 | hp1 | a0001 | c0001 | t0001 | g0293 | AMR | PEL | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| HG02148 | hp2 | a0001 | c0001 | t0004 | g0063 | AMR | PEL | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| HG02165 | hp1 | a0001 | c0001 | t0003 | g0155 | EAS | CDX | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| HG02165 | hp2 | a0001 | c0001 | t0001 | g0274 | EAS | CDX | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| HG02258 | hp1 | a0001 | c0001 | t0001 | g0311 | AFR | ACB | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| HG02258 | hp2 | a0001 | c0001 | t0001 | g0285 | AFR | ACB | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| HG02273 | hp1 | a0001 | c0001 | t0001 | g0235 | AMR | PEL | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| HG02273 | hp2 | a0001 | c0001 | t0003 | g0127 | AMR | PEL | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| HG02280 | hp1 | a0001 | c0001 | t0008 | g0013 | AFR | ACB | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| HG02280 | hp2 | a0001 | c0001 | t0006 | g0114 | AFR | ACB | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| HG02293 | hp1 | a0001 | c0001 | t0001 | g0281 | AMR | PEL | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| HG02293 | hp2 | a0002 | c0004 | t0001 | g0299 | AMR | PEL | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| HG02300 | hp1 | a0001 | c0001 | t0001 | g0093 | AMR | PEL | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| HG02300 | hp2 | a0001 | c0001 | t0003 | g0136 | AMR | PEL | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| HG02451 | hp1 | a0001 | c0001 | t0002 | g0334 | AFR | ACB | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| HG02451 | hp2 | a0001 | c0001 | t0001 | g0306 | AFR | ACB | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| HG02572 | hp1 | a0001 | c0001 | t0002 | g0036 | AFR | GWD | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| HG02572 | hp2 | a0001 | c0001 | t0001 | g0296 | AFR | GWD | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| HG02602 | hp1 | a0001 | c0002 | t0021 | g0216 | SAS | PJL | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| HG02602 | hp2 | a0001 | c0001 | t0003 | g0204 | SAS | PJL | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| HG02615 | hp1 | a0001 | c0001 | t0003 | g0007 | AFR | GWD | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| HG02615 | hp2 | a0001 | c0001 | t0005 | g0075 | AFR | GWD | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| HG02622 | hp1 | a0001 | c0001 | t0001 | g0310 | AFR | GWD | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| HG02622 | hp2 | a0001 | c0001 | t0016 | g0025 | AFR | GWD | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| HG02630 | hp1 | a0001 | c0001 | t0007 | g0106 | AFR | GWD | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| HG02630 | hp2 | a0001 | c0001 | t0002 | g0317 | AFR | GWD | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| HG02647 | hp1 | a0001 | c0001 | t0004 | g0042 | AFR | GWD | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| HG02647 | hp2 | a0001 | c0001 | t0017 | g0022 | AFR | GWD | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| HG02683 | hp1 | a0001 | c0001 | t0015 | g0006 | SAS | PJL | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| HG02683 | hp2 | a0001 | c0001 | t0004 | g0044 | SAS | PJL | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| HG02698 | hp1 | a0001 | c0002 | t0009 | g0211 | SAS | PJL | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| HG02698 | hp2 | a0001 | c0001 | t0003 | g0169 | SAS | PJL | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| HG02717 | hp1 | a0001 | c0001 | t0001 | g0295 | AFR | GWD | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| HG02717 | hp2 | a0001 | c0001 | t0002 | g0320 | AFR | GWD | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| HG02723 | hp1 | a0001 | c0001 | t0005 | g0019 | AFR | GWD | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| HG02723 | hp2 | a0001 | c0001 | t0002 | g0324 | AFR | GWD | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| HG02735 | hp1 | a0001 | c0001 | t0010 | g0048 | SAS | PJL | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| HG02735 | hp2 | a0001 | c0001 | t0001 | g0276 | SAS | PJL | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| HG02738 | hp1 | a0001 | c0001 | t0003 | g0221 | SAS | PJL | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| HG02738 | hp2 | a0001 | c0001 | t0004 | g0069 | SAS | PJL | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| HG02809 | hp1 | a0001 | c0001 | t0002 | g0319 | AFR | GWD | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| HG02809 | hp2 | a0001 | c0001 | t0005 | g0031 | AFR | GWD | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| HG02818 | hp1 | a0001 | c0001 | t0002 | g0220 | AFR | GWD | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| HG02818 | hp2 | a0001 | c0001 | t0008 | g0010 | AFR | GWD | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| HG02886 | hp1 | a0001 | c0001 | t0008 | g0016 | AFR | GWD | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| HG02886 | hp2 | a0001 | c0001 | t0002 | g0341 | AFR | GWD | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| HG02895 | hp1 | a0001 | c0001 | t0007 | g0104 | AFR | GWD | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| HG02895 | hp2 | a0001 | c0001 | t0002 | g0331 | AFR | GWD | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| HG02896 | hp1 | a0001 | c0001 | t0004 | g0035 | AFR | GWD | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| HG02896 | hp2 | a0001 | c0001 | t0002 | g0330 | AFR | GWD | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| HG02922 | hp1 | a0001 | c0001 | t0007 | g0100 | AFR | ESN | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| HG02922 | hp2 | a0001 | c0001 | t0008 | g0011 | AFR | ESN | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| HG02970 | hp1 | a0001 | c0001 | t0004 | g0038 | AFR | ESN | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| HG02970 | hp2 | a0001 | c0001 | t0001 | g0294 | AFR | ESN | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| HG02976 | hp1 | a0001 | c0001 | t0001 | g0229 | AFR | ESN | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| HG02976 | hp2 | a0001 | c0001 | t0008 | g0009 | AFR | ESN | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| HG03017 | hp1 | a0001 | c0001 | t0001 | g0084 | SAS | PJL | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| HG03017 | hp2 | a0001 | c0001 | t0003 | g0154 | SAS | PJL | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| HG03041 | hp1 | a0001 | c0001 | t0002 | g0315 | AFR | GWD | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| HG03041 | hp2 | a0001 | c0001 | t0008 | g0014 | AFR | GWD | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| HG03098 | hp1 | a0001 | c0001 | t0006 | g0109 | AFR | MSL | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| HG03098 | hp2 | a0001 | c0001 | t0008 | g0012 | AFR | MSL | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| HG03130 | hp1 | a0001 | c0001 | t0005 | g0032 | AFR | ESN | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| HG03130 | hp2 | a0001 | c0001 | t0001 | g0297 | AFR | ESN | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| HG03139 | hp1 | a0001 | c0003 | t0004 | g0068 | AFR | ESN | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| HG03139 | hp2 | a0001 | c0001 | t0003 | g0008 | AFR | ESN | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| HG03195 | hp1 | a0001 | c0001 | t0006 | g0110 | AFR | ESN | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| HG03195 | hp2 | a0001 | c0001 | t0005 | g0033 | AFR | ESN | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| HG03209 | hp1 | a0001 | c0001 | t0002 | g0219 | AFR | MSL | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| HG03209 | hp2 | a0001 | c0001 | t0006 | g0111 | AFR | MSL | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| HG03225 | hp1 | a0001 | c0001 | t0002 | g0325 | AFR | MSL | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| HG03225 | hp2 | a0001 | c0001 | t0006 | g0113 | AFR | MSL | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| HG03239 | hp1 | a0001 | c0002 | t0009 | g0209 | SAS | PJL | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| HG03239 | hp2 | a0001 | c0001 | t0001 | g0248 | SAS | PJL | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| HG03453 | hp1 | a0001 | c0001 | t0006 | g0112 | AFR | MSL | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| HG03453 | hp2 | a0001 | c0001 | t0002 | g0218 | AFR | MSL | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| HG03486 | hp1 | a0001 | c0001 | t0001 | g0304 | AFR | MSL | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| HG03486 | hp2 | a0001 | c0001 | t0006 | g0115 | AFR | MSL | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| HG03490 | hp1 | a0001 | c0001 | t0004 | g0052 | SAS | PJL | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| HG03490 | hp2 | a0001 | c0001 | t0001 | g0094 | SAS | PJL | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| HG03491 | hp1 | a0001 | c0001 | t0001 | g0097 | SAS | PJL | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| HG03491 | hp2 | a0001 | c0001 | t0001 | g0225 | SAS | PJL | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| HG03492 | hp1 | a0001 | c0001 | t0004 | g0051 | SAS | PJL | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| HG03492 | hp2 | a0001 | c0001 | t0001 | g0241 | SAS | PJL | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| HG03516 | hp1 | a0001 | c0001 | t0004 | g0037 | AFR | ESN | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| HG03516 | hp2 | a0001 | c0001 | t0007 | g0105 | AFR | ESN | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| HG03540 | hp1 | a0001 | c0001 | t0005 | g0034 | AFR | GWD | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| HG03540 | hp2 | a0001 | c0001 | t0007 | g0102 | AFR | GWD | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| HG03669 | hp1 | a0001 | c0001 | t0004 | g0070 | SAS | PJL | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| HG03669 | hp2 | a0001 | c0001 | t0001 | g0265 | SAS | PJL | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| HG03688 | hp1 | a0001 | c0001 | t0004 | g0065 | SAS | STU | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| HG03688 | hp2 | a0001 | c0001 | t0003 | g0170 | SAS | STU | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| HG03704 | hp1 | a0001 | c0001 | t0001 | g0085 | SAS | PJL | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| HG03704 | hp2 | a0001 | c0001 | t0018 | g0041 | SAS | PJL | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| HG03834 | hp1 | a0001 | c0001 | t0002 | g0329 | SAS | BEB | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| HG03834 | hp2 | a0001 | c0001 | t0007 | g0103 | SAS | BEB | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| HG03942 | hp1 | a0001 | c0001 | t0001 | g0282 | SAS | BEB | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| HG03942 | hp2 | a0001 | c0001 | t0001 | g0079 | SAS | BEB | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| HG04184 | hp1 | a0001 | c0001 | t0003 | g0171 | SAS | BEB | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| HG04184 | hp2 | a0001 | c0001 | t0001 | g0308 | SAS | BEB | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| HG04199 | hp1 | a0001 | c0001 | t0003 | g0202 | SAS | STU | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| HG04199 | hp2 | a0001 | c0001 | t0001 | g0287 | SAS | STU | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| HG04204 | hp1 | a0001 | c0001 | t0003 | g0168 | SAS | STU | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| HG04204 | hp2 | a0001 | c0002 | t0009 | g0215 | SAS | STU | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| HG04228 | hp1 | a0001 | c0001 | t0003 | g0217 | SAS | STU | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| HG04228 | hp2 | a0001 | c0001 | t0004 | g0062 | SAS | STU | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| NA18612 | hp1 | a0001 | c0001 | t0001 | g0249 | EAS | CHB | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| NA18612 | hp2 | a0001 | c0001 | t0003 | g0161 | EAS | CHB | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| NA18747 | hp1 | a0001 | c0001 | t0003 | g0120 | EAS | CHB | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| NA18747 | hp2 | a0001 | c0001 | t0001 | g0263 | EAS | CHB | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| NA18906 | hp1 | a0001 | c0001 | t0001 | g0312 | AFR | YRI | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| NA18906 | hp2 | a0001 | c0001 | t0006 | g0116 | AFR | YRI | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| NA18939 | hp1 | a0001 | c0001 | t0001 | g0268 | EAS | JPT | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| NA18939 | hp2 | a0001 | c0001 | t0004 | g0059 | EAS | JPT | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| NA18943 | hp1 | a0001 | c0001 | t0003 | g0175 | EAS | JPT | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| NA18943 | hp2 | a0001 | c0001 | t0001 | g0288 | EAS | JPT | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| NA18944 | hp1 | a0001 | c0001 | t0002 | g0150 | EAS | JPT | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| NA18944 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| NA18948 | hp1 | a0001 | c0001 | t0001 | g0291 | EAS | JPT | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| NA18948 | hp2 | a0001 | c0001 | t0002 | g0123 | EAS | JPT | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| NA18950 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| NA18950 | hp2 | a0001 | c0001 | t0002 | g0140 | EAS | JPT | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| NA18951 | hp1 | a0001 | c0001 | t0002 | g0130 | EAS | JPT | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| NA18951 | hp2 | a0001 | c0001 | t0001 | g0258 | EAS | JPT | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| NA18953 | hp1 | a0001 | c0001 | t0003 | g0182 | EAS | JPT | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| NA18953 | hp2 | a0001 | c0001 | t0001 | g0252 | EAS | JPT | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| NA18956 | hp1 | a0001 | c0001 | t0003 | g0159 | EAS | JPT | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| NA18956 | hp2 | a0001 | c0001 | t0001 | g0272 | EAS | JPT | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| NA18957 | hp1 | a0001 | c0001 | t0003 | g0172 | EAS | JPT | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| NA18957 | hp2 | a0001 | c0001 | t0002 | g0138 | EAS | JPT | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| NA18959 | hp1 | a0001 | c0001 | t0001 | g0253 | EAS | JPT | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| NA18959 | hp2 | a0001 | c0001 | t0003 | g0156 | EAS | JPT | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| NA18962 | hp1 | a0001 | c0001 | t0003 | g0174 | EAS | JPT | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| NA18962 | hp2 | a0001 | c0001 | t0001 | g0254 | EAS | JPT | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| NA18966 | hp1 | a0001 | c0001 | t0022 | g0201 | EAS | JPT | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| NA18966 | hp2 | a0001 | c0001 | t0003 | g0183 | EAS | JPT | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| NA18967 | hp1 | a0001 | c0001 | t0002 | g0198 | EAS | JPT | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| NA18967 | hp2 | a0001 | c0001 | t0001 | g0271 | EAS | JPT | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| NA18968 | hp1 | a0001 | c0001 | t0003 | g0207 | EAS | JPT | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| NA18968 | hp2 | a0001 | c0001 | t0001 | g0250 | EAS | JPT | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| NA18969 | hp1 | a0001 | c0001 | t0001 | g0262 | EAS | JPT | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| NA18969 | hp2 | a0001 | c0001 | t0011 | g0158 | EAS | JPT | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| NA18970 | hp1 | a0001 | c0001 | t0012 | g0005 | EAS | JPT | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| NA18970 | hp2 | a0001 | c0001 | t0001 | g0230 | EAS | JPT | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| NA18972 | hp1 | a0001 | c0001 | t0003 | g0208 | EAS | JPT | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| NA18972 | hp2 | a0001 | c0001 | t0001 | g0301 | EAS | JPT | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| NA18974 | hp1 | a0001 | c0001 | t0003 | g0147 | EAS | JPT | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| NA18974 | hp2 | a0001 | c0001 | t0002 | g0180 | EAS | JPT | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| NA18975 | hp1 | a0001 | c0001 | t0003 | g0164 | EAS | JPT | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| NA18975 | hp2 | a0001 | c0001 | t0001 | g0302 | EAS | JPT | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| NA18977 | hp1 | a0001 | c0001 | t0002 | g0131 | EAS | JPT | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| NA18977 | hp2 | a0001 | c0001 | t0001 | g0242 | EAS | JPT | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| NA18978 | hp1 | a0001 | c0001 | t0002 | g0335 | EAS | JPT | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| NA18978 | hp2 | a0001 | c0001 | t0003 | g0162 | EAS | JPT | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| NA18979 | hp1 | a0001 | c0001 | t0002 | g0318 | EAS | JPT | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| NA18979 | hp2 | a0001 | c0001 | t0001 | g0255 | EAS | JPT | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| NA18983 | hp1 | a0001 | c0001 | t0001 | g0257 | EAS | JPT | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| NA18983 | hp2 | a0001 | c0001 | t0003 | g0200 | EAS | JPT | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| NA18990 | hp1 | a0001 | c0001 | t0003 | g0195 | EAS | JPT | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| NA18990 | hp2 | a0001 | c0001 | t0004 | g0061 | EAS | JPT | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| NA18991 | hp1 | a0001 | c0001 | t0001 | g0231 | EAS | JPT | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| NA18991 | hp2 | a0001 | c0001 | t0002 | g0187 | EAS | JPT | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| NA18992 | hp1 | a0001 | c0001 | t0003 | g0124 | EAS | JPT | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| NA18992 | hp2 | a0001 | c0001 | t0014 | g0227 | EAS | JPT | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| NA18994 | hp1 | a0001 | c0001 | t0001 | g0243 | EAS | JPT | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| NA18994 | hp2 | a0001 | c0001 | t0002 | g0188 | EAS | JPT | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| NA18995 | hp1 | a0001 | c0001 | t0002 | g0185 | EAS | JPT | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| NA18995 | hp2 | a0001 | c0001 | t0004 | g0067 | EAS | JPT | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| NA18997 | hp1 | a0001 | c0001 | t0001 | g0309 | EAS | JPT | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| NA18997 | hp2 | a0001 | c0001 | t0002 | g0186 | EAS | JPT | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| NA18998 | hp1 | a0001 | c0001 | t0002 | g0118 | EAS | JPT | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| NA18998 | hp2 | a0001 | c0001 | t0001 | g0244 | EAS | JPT | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| NA18999 | hp1 | a0001 | c0001 | t0003 | g0165 | EAS | JPT | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| NA18999 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| NA19000 | hp1 | a0001 | c0001 | t0002 | g0149 | EAS | JPT | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| NA19000 | hp2 | a0001 | c0001 | t0004 | g0064 | EAS | JPT | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| NA19001 | hp1 | a0001 | c0001 | t0003 | g0125 | EAS | JPT | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| NA19001 | hp2 | a0001 | c0001 | t0004 | g0045 | EAS | JPT | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| NA19004 | hp1 | a0001 | c0001 | t0004 | g0060 | EAS | JPT | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| NA19004 | hp2 | a0001 | c0001 | t0012 | g0167 | EAS | JPT | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| NA19009 | hp1 | a0001 | c0001 | t0002 | g0151 | EAS | JPT | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| NA19009 | hp2 | a0001 | c0001 | t0004 | g0071 | EAS | JPT | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| NA19011 | hp1 | a0001 | c0001 | t0002 | g0137 | EAS | JPT | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| NA19011 | hp2 | a0001 | c0001 | t0001 | g0245 | EAS | JPT | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| NA19043 | hp1 | a0001 | c0001 | t0007 | g0099 | AFR | LWK | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| NA19043 | hp2 | a0001 | c0001 | t0006 | g0107 | AFR | LWK | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| NA19054 | hp1 | a0001 | c0001 | t0002 | g0139 | EAS | JPT | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| NA19054 | hp2 | a0001 | c0001 | t0004 | g0046 | EAS | JPT | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| NA19057 | hp1 | a0001 | c0001 | t0002 | g0145 | EAS | JPT | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| NA19057 | hp2 | a0001 | c0001 | t0002 | g0326 | EAS | JPT | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| NA19058 | hp1 | a0001 | c0001 | t0012 | g0005 | EAS | JPT | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| NA19058 | hp2 | a0001 | c0001 | t0004 | g0074 | EAS | JPT | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| NA19060 | hp1 | a0001 | c0001 | t0002 | g0184 | EAS | JPT | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| NA19060 | hp2 | a0001 | c0001 | t0004 | g0049 | EAS | JPT | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| NA19068 | hp1 | a0001 | c0001 | t0001 | g0247 | EAS | JPT | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| NA19068 | hp2 | a0001 | c0001 | t0001 | g0259 | EAS | JPT | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| NA19070 | hp1 | a0001 | c0001 | t0002 | g0333 | EAS | JPT | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| NA19070 | hp2 | a0001 | c0001 | t0002 | g0142 | EAS | JPT | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| NA19075 | hp1 | a0001 | c0001 | t0001 | g0307 | EAS | JPT | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| NA19075 | hp2 | a0001 | c0001 | t0004 | g0073 | EAS | JPT | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| NA19077 | hp1 | a0001 | c0001 | t0003 | g0181 | EAS | JPT | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| NA19077 | hp2 | a0001 | c0001 | t0001 | g0298 | EAS | JPT | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| NA19079 | hp1 | a0001 | c0001 | t0004 | g0050 | EAS | JPT | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| NA19079 | hp2 | a0001 | c0001 | t0003 | g0199 | EAS | JPT | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| NA19080 | hp1 | a0001 | c0001 | t0001 | g0283 | EAS | JPT | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| NA19080 | hp2 | a0001 | c0001 | t0002 | g0004 | EAS | JPT | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| NA19082 | hp1 | a0001 | c0001 | t0004 | g0047 | EAS | JPT | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| NA19082 | hp2 | a0001 | c0001 | t0002 | g0119 | EAS | JPT | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| NA19083 | hp1 | a0001 | c0001 | t0001 | g0303 | EAS | JPT | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| NA19083 | hp2 | a0001 | c0001 | t0003 | g0206 | EAS | JPT | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| NA19084 | hp1 | a0001 | c0001 | t0003 | g0166 | EAS | JPT | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| NA19084 | hp2 | a0001 | c0001 | t0001 | g0273 | EAS | JPT | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| NA19086 | hp1 | a0001 | c0001 | t0003 | g0205 | EAS | JPT | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| NA19086 | hp2 | a0001 | c0001 | t0004 | g0027 | EAS | JPT | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| NA19087 | hp1 | a0001 | c0001 | t0002 | g0327 | EAS | JPT | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| NA19087 | hp2 | a0001 | c0001 | t0001 | g0246 | EAS | JPT | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| NA19088 | hp1 | a0001 | c0001 | t0002 | g0328 | EAS | JPT | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| NA19088 | hp2 | a0001 | c0001 | t0002 | g0144 | EAS | JPT | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| NA19240 | hp1 | a0001 | c0001 | t0005 | g0030 | AFR | YRI | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| NA19240 | hp2 | a0001 | c0001 | t0002 | g0342 | AFR | YRI | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| NA20752 | hp1 | a0001 | c0001 | t0003 | g0178 | EUR | TSI | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| NA20752 | hp2 | a0001 | c0001 | t0002 | g0339 | EUR | TSI | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| NA20805 | hp1 | a0001 | c0001 | t0001 | g0087 | EUR | TSI | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| NA20805 | hp2 | a0001 | c0001 | t0003 | g0337 | EUR | TSI | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| NA20905 | hp1 | a0001 | c0001 | t0003 | g0152 | SAS | GIH | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| NA20905 | hp2 | a0001 | c0001 | t0004 | g0056 | SAS | GIH | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| HG01123 | hp1 | a0001 | c0001 | t0003 | g0191 | AMR | CLM | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| HG01123 | hp2 | a0001 | c0001 | t0001 | g0091 | AMR | CLM | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| HG02109 | hp1 | a0001 | c0001 | t0006 | g0117 | AFR | ACB | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| HG02109 | hp2 | a0001 | c0001 | t0001 | g0286 | AFR | ACB | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| HG02486 | hp1 | a0001 | c0001 | t0003 | g0126 | AFR | ACB | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| HG02486 | hp2 | a0001 | c0001 | t0005 | g0020 | AFR | ACB | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| HG02559 | hp1 | a0001 | c0001 | t0008 | g0017 | AFR | ACB | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| HG02559 | hp2 | a0001 | c0001 | t0001 | g0078 | AFR | ACB | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| HG03471 | hp1 | a0001 | c0001 | t0001 | g0305 | AFR | MSL | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| HG03471 | hp2 | a0001 | c0001 | t0002 | g0323 | AFR | MSL | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| NA18955 | hp1 | a0001 | c0001 | t0001 | g0270 | EAS | JPT | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| NA18955 | hp2 | a0001 | c0001 | t0003 | g0173 | EAS | JPT | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| NA21309 | hp1 | a0001 | c0001 | t0004 | g0066 | AFR | LWK | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| NA21309 | hp2 | a0001 | c0001 | t0008 | g0344 | AFR | LWK | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0010 | g0055 | REF | REF | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| homoSapiens_grch38 | hp1 | a0001 | c0001 | t0003 | g0076 | REF | REF | MFSD14B_chr9_94369569_94466042 | MFSD14B | chr9 | 94369569 | 94466042 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr9:94429217
|
C | G | 1 | a0002 | 1 | HG02293.hp2 | missense_variant | MODERATE | c.233C>G | p.Thr78Arg | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 3/12 | 484/3402 | 233/1521 | 78/506 | chr9 | 94429217 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr9:94446849
|
T | C | 1 | a0001c0003 | 1 | HG03139.hp1 | synonymous_variant | LOW | c.756T>C | p.Ser252Ser | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 7/12 | 1007/3402 | 756/1521 | 252/506 | chr9 | 94446849 | ||
| chr9:94459181
|
G | A | 1 | a0001c0002 | 8 | HG00140.hp2 HG00741.hp2 HG01255.hp2 others(5): Show |
synonymous_variant | LOW | c.1290G>A | p.Pro430Pro | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 12/12 | 1541/3402 | 1290/1521 | 430/506 | chr9 | 94459181 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr9:94374580
|
G | C | 1 | a0001c0001t0015 | 1 | HG02683.hp1 | 5_prime_UTR_variant | MODIFIER | c.-240G>C | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 1/12 | 240 | chr9 | 94374580 | |||||
| chr9:94374585
|
G | C | 1 | a0001c0001t0016 | 1 | HG02622.hp2 | 5_prime_UTR_variant | MODIFIER | c.-235G>C | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 1/12 | 235 | chr9 | 94374585 | |||||
| chr9:94374602
|
A | C | 1 | a0001c0001t0015 | 1 | HG02683.hp1 | 5_prime_UTR_variant | MODIFIER | c.-218A>C | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 1/12 | 218 | chr9 | 94374602 | |||||
| chr9:94374606
|
G | C | 1 | a0001c0001t0017 | 1 | HG02647.hp2 | 5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-214G>C | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 1/12 | chr9 | 94374606 | ||||||
| chr9:94374680
|
CGGCGCCG others(5): Show |
C | 1 | a0001c0001t0015 | 1 | HG02683.hp1 | 5_prime_UTR_variant | MODIFIER | c.-128_-117delTGGCGC others(6): Show |
MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 1/12 | 117 | INFO_REALIGN_3_PRIME | chr9 | 94374680 | ||||
| chr9:94374796
|
G | A | 1 | a0001c0001t0015 | 1 | HG02683.hp1 | 5_prime_UTR_variant | MODIFIER | c.-24G>A | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 1/12 | 24 | chr9 | 94374796 | |||||
| chr9:94459443
|
C | T | 1 | a0001c0001t0023 | 1 | HG02135.hp2 | 3_prime_UTR_variant | MODIFIER | c.*31C>T | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 12/12 | 31 | chr9 | 94459443 | |||||
| chr9:94459572
|
GT | G | 14 | a0001c0001t0001a0001c0001t0002a0001c0001t0006others(11): Show | 222 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(219): Show |
3_prime_UTR_variant | MODIFIER | c.*172delT | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 12/12 | 172 | INFO_REALIGN_3_PRIME | chr9 | 94459572 | ||||
| chr9:94459572
|
GTT | G | 6 | a0001c0001t0004a0001c0001t0005a0001c0001t0010others(3): Show | 56 | HG00597.hp1 HG00639.hp2 HG00642.hp1 others(53): Show |
3_prime_UTR_variant | MODIFIER | c.*171_*172delTT | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 12/12 | 171 | INFO_REALIGN_3_PRIME | chr9 | 94459572 | ||||
| chr9:94459595
|
C | CT | 5 | a0001c0001t0004a0001c0001t0005a0001c0001t0010others(2): Show | 54 | HG00597.hp1 HG00639.hp2 HG00642.hp1 others(51): Show |
3_prime_UTR_variant | MODIFIER | c.*194dupT | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 12/12 | 195 | INFO_REALIGN_3_PRIME | chr9 | 94459595 | ||||
| chr9:94459673
|
G | A | 1 | a0001c0001t0017 | 1 | HG02647.hp2 | 3_prime_UTR_variant | MODIFIER | c.*261G>A | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 12/12 | 261 | chr9 | 94459673 | |||||
| chr9:94459674
|
G | T | 1 | a0001c0001t0022 | 1 | NA18966.hp1 | 3_prime_UTR_variant | MODIFIER | c.*262G>T | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 12/12 | 262 | chr9 | 94459674 | |||||
| chr9:94459765
|
G | A | 2 | a0001c0002t0009a0001c0002t0021 | 8 | HG00140.hp2 HG00741.hp2 HG01255.hp2 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*353G>A | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 12/12 | 353 | chr9 | 94459765 | |||||
| chr9:94460351
|
A | G | 1 | a0001c0001t0012 | 3 | NA18970.hp1 NA19004.hp2 NA19058.hp1 |
3_prime_UTR_variant | MODIFIER | c.*939A>G | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 12/12 | 939 | chr9 | 94460351 | |||||
| chr9:94460461
|
A | C | 1 | a0001c0001t0018 | 1 | HG03704.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1049A>C | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 12/12 | 1049 | chr9 | 94460461 | |||||
| chr9:94460497
|
C | CTGAG | 4 | a0001c0001t0004a0001c0001t0010a0001c0001t0018others(1): Show | 41 | HG00597.hp1 HG00639.hp2 HG00642.hp1 others(38): Show |
3_prime_UTR_variant | MODIFIER | c.*1087_*1090dupGAGT | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 12/12 | 1091 | INFO_REALIGN_3_PRIME | chr9 | 94460497 | ||||
| chr9:94460507
|
C | T | 1 | a0001c0001t0008 | 10 | HG01081.hp1 HG02280.hp1 HG02559.hp1 others(7): Show |
3_prime_UTR_variant | MODIFIER | c.*1095C>T | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 12/12 | 1095 | chr9 | 94460507 | |||||
| chr9:94460539
|
T | C | 1 | a0001c0001t0019 | 1 | HG01361.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1127T>C | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 12/12 | 1127 | chr9 | 94460539 | |||||
| chr9:94460606
|
GGC | G | 5 | a0001c0001t0004a0001c0001t0005a0001c0001t0010others(2): Show | 54 | HG00597.hp1 HG00639.hp2 HG00642.hp1 others(51): Show |
3_prime_UTR_variant | MODIFIER | c.*1195_*1196delGC | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 12/12 | 1195 | chr9 | 94460606 | |||||
| chr9:94460609
|
C | T | 5 | a0001c0001t0004a0001c0001t0005a0001c0001t0010others(2): Show | 54 | HG00597.hp1 HG00639.hp2 HG00642.hp1 others(51): Show |
3_prime_UTR_variant | MODIFIER | c.*1197C>T | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 12/12 | 1197 | chr9 | 94460609 | |||||
| chr9:94460610
|
C | G | 5 | a0001c0001t0004a0001c0001t0005a0001c0001t0010others(2): Show | 54 | HG00597.hp1 HG00639.hp2 HG00642.hp1 others(51): Show |
3_prime_UTR_variant | MODIFIER | c.*1198C>G | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 12/12 | 1198 | chr9 | 94460610 | |||||
| chr9:94460682
|
AT | A | 4 | a0001c0001t0007a0001c0001t0011a0001c0002t0009others(1): Show | 22 | HG00140.hp2 HG00544.hp1 HG00741.hp2 others(19): Show |
3_prime_UTR_variant | MODIFIER | c.*1282delT | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 12/12 | 1282 | INFO_REALIGN_3_PRIME | chr9 | 94460682 | ||||
| chr9:94460682
|
ATT | A | 14 | a0001c0001t0001a0001c0001t0004a0001c0001t0005others(11): Show | 183 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(180): Show |
3_prime_UTR_variant | MODIFIER | c.*1281_*1282delTT | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 12/12 | 1281 | INFO_REALIGN_3_PRIME | chr9 | 94460682 | ||||
| chr9:94460683
|
T | A | 1 | a0001c0001t0006 | 11 | HG01243.hp2 HG02109.hp1 HG02280.hp2 others(8): Show |
3_prime_UTR_variant | MODIFIER | c.*1271T>A | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 12/12 | 1271 | chr9 | 94460683 | |||||
| chr9:94460847
|
A | G | 1 | a0001c0001t0020 | 1 | HG01255.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1435A>G | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 12/12 | 1435 | chr9 | 94460847 | |||||
| chr9:94460931
|
C | CT | 8 | a0001c0001t0001a0001c0001t0008a0001c0001t0010others(5): Show | 130 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(127): Show |
3_prime_UTR_variant | MODIFIER | c.*1527dupT | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 12/12 | 1528 | INFO_REALIGN_3_PRIME | chr9 | 94460931 | ||||
| chr9:94461012
|
C | G | 8 | a0001c0001t0001a0001c0001t0008a0001c0001t0013others(5): Show | 128 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(125): Show |
3_prime_UTR_variant | MODIFIER | c.*1600C>G | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 12/12 | 1600 | chr9 | 94461012 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr9:94374951
|
C | T | 1 | a0001c0001t0008g0344 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.108+24C>T | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 1/11 | chr9 | 94374951 | ||||||
| chr9:94374952
|
T | G | 1 | a0001c0001t0015g0006 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.108+25T>G | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 1/11 | chr9 | 94374952 | ||||||
| chr9:94374961
|
C | G | 1 | a0001c0001t0015g0006 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.108+34C>G | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 1/11 | chr9 | 94374961 | ||||||
| chr9:94374963
|
C | A | 2 | a0001c0001t0003g0007a0001c0001t0003g0008 | 2 | HG02615.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.108+36C>A | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 1/11 | chr9 | 94374963 | ||||||
| chr9:94375051
|
G | T | 33 | a0001c0001t0002g0315a0001c0001t0002g0316a0001c0001t0002g0317others(30): Show | 33 | HG00639.hp1 HG01070.hp2 HG01071.hp2 others(30): Show |
intron_variant | MODIFIER | c.108+124G>T | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 1/11 | chr9 | 94375051 | ||||||
| chr9:94375108
|
G | T | 89 | a0001c0001t0001g0001a0001c0001t0001g0225a0001c0001t0001g0226others(86): Show | 91 | HG00323.hp2 HG00408.hp2 HG00423.hp1 others(88): Show |
intron_variant | MODIFIER | c.108+181G>T | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 1/11 | chr9 | 94375108 | ||||||
| chr9:94375248
|
A | C | 159 | a0001c0001t0002g0004a0001c0001t0002g0118a0001c0001t0002g0119others(156): Show | 161 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(158): Show |
intron_variant | MODIFIER | c.108+321A>C | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 1/11 | chr9 | 94375248 | ||||||
| chr9:94375263
|
CAGGT | C | 11 | a0001c0001t0008g0009a0001c0001t0008g0010a0001c0001t0008g0011others(8): Show | 11 | HG01081.hp1 HG02280.hp1 HG02559.hp1 others(8): Show |
intron_variant | MODIFIER | c.108+340_108+343del others(4): Show |
MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr9 | 94375263 | |||||
| chr9:94375412
|
A | G | 159 | a0001c0001t0002g0004a0001c0001t0002g0118a0001c0001t0002g0119others(156): Show | 161 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(158): Show |
intron_variant | MODIFIER | c.108+485A>G | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 1/11 | chr9 | 94375412 | ||||||
| chr9:94375467
|
C | G | 1 | a0001c0001t0015g0006 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.108+540C>G | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 1/11 | chr9 | 94375467 | ||||||
| chr9:94375486
|
G | A | 320 | a0001c0001t0001g0001a0001c0001t0001g0225a0001c0001t0001g0226others(317): Show | 325 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(322): Show |
intron_variant | MODIFIER | c.108+559G>A | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 1/11 | chr9 | 94375486 | ||||||
| chr9:94375553
|
G | T | 1 | a0001c0001t0001g0312 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.108+626G>T | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 1/11 | chr9 | 94375553 | ||||||
| chr9:94375563
|
A | G | 1 | a0001c0001t0015g0006 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.108+636A>G | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 1/11 | chr9 | 94375563 | ||||||
| chr9:94375569
|
C | G | 1 | a0001c0001t0015g0006 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.108+642C>G | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 1/11 | chr9 | 94375569 | ||||||
| chr9:94375622
|
A | AT | 58 | a0001c0001t0001g0097a0001c0001t0001g0098a0001c0001t0002g0029others(55): Show | 59 | HG00280.hp2 HG00544.hp1 HG00597.hp1 others(56): Show |
intron_variant | MODIFIER | c.108+707dupT | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr9 | 94375622 | |||||
| chr9:94375657
|
A | G | 1 | a0001c0001t0015g0006 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.108+730A>G | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 1/11 | chr9 | 94375657 | ||||||
| chr9:94375666
|
C | G | 1 | a0001c0001t0003g0222 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.108+739C>G | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 1/11 | chr9 | 94375666 | ||||||
| chr9:94375733
|
A | G | 1 | a0001c0001t0002g0343 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.108+806A>G | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 1/11 | chr9 | 94375733 | ||||||
| chr9:94375955
|
C | T | 1 | a0001c0001t0003g0221 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.108+1028C>T | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 1/11 | chr9 | 94375955 | ||||||
| chr9:94375983
|
A | G | 2 | a0001c0001t0001g0310a0001c0001t0001g0311 | 2 | HG02258.hp1 HG02622.hp1 |
intron_variant | MODIFIER | c.108+1056A>G | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 1/11 | chr9 | 94375983 | ||||||
| chr9:94376194
|
G | T | 1 | a0001c0001t0005g0075 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.108+1267G>T | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 1/11 | chr9 | 94376194 | ||||||
| chr9:94376452
|
G | A | 1 | a0001c0001t0010g0026 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.108+1525G>A | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 1/11 | chr9 | 94376452 | ||||||
| chr9:94376738
|
T | C | 9 | a0001c0001t0007g0099a0001c0001t0007g0100a0001c0001t0007g0101others(6): Show | 9 | HG00544.hp1 HG01884.hp1 HG02630.hp1 others(6): Show |
intron_variant | MODIFIER | c.108+1811T>C | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 1/11 | chr9 | 94376738 | ||||||
| chr9:94376760
|
C | G | 3 | a0001c0001t0002g0218a0001c0001t0002g0219a0001c0001t0002g0220 | 3 | HG02818.hp1 HG03209.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.108+1833C>G | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 1/11 | chr9 | 94376760 | ||||||
| chr9:94376848
|
C | T | 1 | a0001c0001t0003g0217 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.108+1921C>T | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 1/11 | chr9 | 94376848 | ||||||
| chr9:94376879
|
C | T | 339 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0081others(336): Show | 345 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(342): Show |
intron_variant | MODIFIER | c.108+1952C>T | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 1/11 | chr9 | 94376879 | ||||||
| chr9:94376880
|
G | A | 11 | a0001c0001t0006g0107a0001c0001t0006g0108a0001c0001t0006g0109others(8): Show | 11 | HG01243.hp2 HG02109.hp1 HG02280.hp2 others(8): Show |
intron_variant | MODIFIER | c.108+1953G>A | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 1/11 | chr9 | 94376880 | ||||||
| chr9:94376945
|
G | T | 8 | a0001c0002t0009g0209a0001c0002t0009g0210a0001c0002t0009g0211others(5): Show | 8 | HG00140.hp2 HG00741.hp2 HG01255.hp2 others(5): Show |
intron_variant | MODIFIER | c.108+2018G>T | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 1/11 | chr9 | 94376945 | ||||||
| chr9:94376946
|
A | T | 8 | a0001c0002t0009g0209a0001c0002t0009g0210a0001c0002t0009g0211others(5): Show | 8 | HG00140.hp2 HG00741.hp2 HG01255.hp2 others(5): Show |
intron_variant | MODIFIER | c.108+2019A>T | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 1/11 | chr9 | 94376946 | ||||||
| chr9:94377090
|
A | T | 1 | a0001c0001t0003g0208 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.108+2163A>T | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 1/11 | chr9 | 94377090 | ||||||
| chr9:94377267
|
T | G | 29 | a0001c0001t0002g0315a0001c0001t0002g0316a0001c0001t0002g0317others(26): Show | 29 | HG00639.hp1 HG01109.hp2 HG01255.hp1 others(26): Show |
intron_variant | MODIFIER | c.108+2340T>G | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 1/11 | chr9 | 94377267 | ||||||
| chr9:94377384
|
GT | G | 120 | a0001c0001t0002g0029a0001c0001t0002g0036a0001c0001t0002g0039others(117): Show | 121 | HG00140.hp2 HG00544.hp1 HG00597.hp1 others(118): Show |
intron_variant | MODIFIER | c.108+2468delT | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr9 | 94377384 | |||||
| chr9:94377385
|
T | G | 1 | a0001c0001t0002g0118 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.108+2458T>G | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 1/11 | chr9 | 94377385 | ||||||
| chr9:94377498
|
T | G | 4 | a0001c0001t0008g0009a0001c0001t0008g0010a0001c0001t0008g0011others(1): Show | 4 | HG02818.hp2 HG02922.hp2 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.108+2571T>G | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 1/11 | chr9 | 94377498 | ||||||
| chr9:94377530
|
T | A | 11 | a0001c0001t0006g0107a0001c0001t0006g0108a0001c0001t0006g0109others(8): Show | 11 | HG01243.hp2 HG02109.hp1 HG02280.hp2 others(8): Show |
intron_variant | MODIFIER | c.108+2603T>A | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 1/11 | chr9 | 94377530 | ||||||
| chr9:94377533
|
C | CT | 31 | a0001c0001t0002g0315a0001c0001t0002g0316a0001c0001t0002g0317others(28): Show | 31 | HG00639.hp1 HG01109.hp2 HG01255.hp1 others(28): Show |
intron_variant | MODIFIER | c.108+2626dupT | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr9 | 94377533 | |||||
| chr9:94377533
|
C | CTT | 14 | a0001c0001t0002g0339a0001c0001t0003g0206a0001c0001t0003g0207others(11): Show | 14 | HG01243.hp2 HG02109.hp1 HG02280.hp2 others(11): Show |
intron_variant | MODIFIER | c.108+2625_108+2626d others(4): Show |
MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr9 | 94377533 | |||||
| chr9:94377533
|
CT | C | 117 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0082others(114): Show | 120 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(117): Show |
intron_variant | MODIFIER | c.108+2626delT | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr9 | 94377533 | |||||
| chr9:94377533
|
CTT | C | 58 | a0001c0001t0001g0081a0001c0001t0001g0225a0001c0001t0002g0029others(55): Show | 59 | HG00597.hp1 HG00639.hp2 HG00642.hp1 others(56): Show |
intron_variant | MODIFIER | c.108+2625_108+2626d others(4): Show |
MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr9 | 94377533 | |||||
| chr9:94377553
|
T | A | 58 | a0001c0001t0002g0029a0001c0001t0002g0036a0001c0001t0002g0039others(55): Show | 59 | HG00597.hp1 HG00639.hp2 HG00642.hp1 others(56): Show |
intron_variant | MODIFIER | c.108+2626T>A | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 1/11 | chr9 | 94377553 | ||||||
| chr9:94377553
|
T | TA | 22 | a0001c0001t0002g0119a0001c0001t0002g0218a0001c0001t0002g0219others(19): Show | 22 | HG00140.hp2 HG00544.hp1 HG00741.hp2 others(19): Show |
intron_variant | MODIFIER | c.108+2628dupA | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr9 | 94377553 | |||||
| chr9:94377553
|
T | TTA | 85 | a0001c0001t0002g0004a0001c0001t0002g0118a0001c0001t0002g0123others(82): Show | 87 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(84): Show |
intron_variant | MODIFIER | c.108+2626_108+2627i others(4): Show |
MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 1/11 | chr9 | 94377553 | ||||||
| chr9:94377553
|
T | TTTA | 6 | a0001c0001t0002g0224a0001c0001t0003g0202a0001c0001t0003g0203others(3): Show | 6 | HG01934.hp2 HG02055.hp2 HG02602.hp2 others(3): Show |
intron_variant | MODIFIER | c.108+2626_108+2627i others(5): Show |
MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 1/11 | chr9 | 94377553 | ||||||
| chr9:94377724
|
C | T | 1 | a0001c0001t0001g0311 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.108+2797C>T | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 1/11 | chr9 | 94377724 | ||||||
| chr9:94377808
|
A | G | 2 | a0001c0001t0004g0071a0001c0001t0004g0072 | 2 | HG00597.hp1 NA19009.hp2 |
intron_variant | MODIFIER | c.108+2881A>G | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 1/11 | chr9 | 94377808 | ||||||
| chr9:94377836
|
G | A | 9 | a0001c0001t0007g0099a0001c0001t0007g0100a0001c0001t0007g0101others(6): Show | 9 | HG00544.hp1 HG01884.hp1 HG02630.hp1 others(6): Show |
intron_variant | MODIFIER | c.108+2909G>A | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 1/11 | chr9 | 94377836 | ||||||
| chr9:94378018
|
C | T | 11 | a0001c0001t0006g0107a0001c0001t0006g0108a0001c0001t0006g0109others(8): Show | 11 | HG01243.hp2 HG02109.hp1 HG02280.hp2 others(8): Show |
intron_variant | MODIFIER | c.108+3091C>T | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 1/11 | chr9 | 94378018 | ||||||
| chr9:94378063
|
CACTGCAC others(16): Show |
C | 11 | a0001c0001t0001g0080a0001c0001t0008g0009a0001c0001t0008g0010others(8): Show | 11 | HG01081.hp1 HG01358.hp1 HG02280.hp1 others(8): Show |
intron_variant | MODIFIER | c.108+3161_108+3183d others(25): Show |
MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr9 | 94378063 | |||||
| chr9:94378082
|
G | A | 1 | a0001c0001t0017g0022 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.108+3155G>A | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 1/11 | chr9 | 94378082 | ||||||
| chr9:94378113
|
G | A | 1 | a0001c0001t0002g0339 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.108+3186G>A | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 1/11 | chr9 | 94378113 | ||||||
| chr9:94378126
|
C | CA | 161 | a0001c0001t0001g0226a0001c0001t0002g0004a0001c0001t0002g0118others(158): Show | 163 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(160): Show |
intron_variant | MODIFIER | c.108+3212dupA | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr9 | 94378126 | |||||
| chr9:94378260
|
T | C | 217 | a0001c0001t0002g0004a0001c0001t0002g0029a0001c0001t0002g0036others(214): Show | 220 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(217): Show |
intron_variant | MODIFIER | c.108+3333T>C | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 1/11 | chr9 | 94378260 | ||||||
| chr9:94378387
|
C | A | 1 | a0001c0001t0017g0022 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.108+3460C>A | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 1/11 | chr9 | 94378387 | ||||||
| chr9:94378501
|
A | G | 216 | a0001c0001t0002g0004a0001c0001t0002g0029a0001c0001t0002g0036others(213): Show | 219 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(216): Show |
intron_variant | MODIFIER | c.108+3574A>G | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 1/11 | chr9 | 94378501 | ||||||
| chr9:94378501
|
A | T | 2 | a0001c0001t0003g0200a0001c0001t0003g0205 | 2 | NA18983.hp2 NA19086.hp1 |
intron_variant | MODIFIER | c.108+3574A>T | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 1/11 | chr9 | 94378501 | ||||||
| chr9:94378559
|
C | T | 3 | a0001c0001t0003g0337a0001c0001t0007g0336a0001c0001t0007g0338 | 3 | HG01256.hp2 HG01496.hp2 NA20805.hp2 |
intron_variant | MODIFIER | c.108+3632C>T | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 1/11 | chr9 | 94378559 | ||||||
| chr9:94378684
|
C | G | 10 | a0001c0001t0008g0009a0001c0001t0008g0010a0001c0001t0008g0011others(7): Show | 10 | HG01081.hp1 HG02280.hp1 HG02559.hp1 others(7): Show |
intron_variant | MODIFIER | c.108+3757C>G | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 1/11 | chr9 | 94378684 | ||||||
| chr9:94378792
|
T | C | 1 | a0001c0001t0004g0027 | 1 | NA19086.hp2 | intron_variant | MODIFIER | c.108+3865T>C | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 1/11 | chr9 | 94378792 | ||||||
| chr9:94378937
|
G | A | 1 | a0001c0001t0014g0227 | 1 | NA18992.hp2 | intron_variant | MODIFIER | c.108+4010G>A | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 1/11 | chr9 | 94378937 | ||||||
| chr9:94379052
|
C | T | 1 | a0001c0001t0003g0199 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.108+4125C>T | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 1/11 | chr9 | 94379052 | ||||||
| chr9:94379089
|
C | CTTTTTTT others(4): Show |
6 | a0001c0001t0002g0119a0001c0001t0002g0123a0001c0001t0003g0124others(3): Show | 6 | HG02273.hp2 HG02486.hp1 NA18948.hp2 others(3): Show |
intron_variant | MODIFIER | c.108+4166_108+4176d others(13): Show |
MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr9 | 94379089 | |||||
| chr9:94379089
|
C | CTTTTTTT others(5): Show |
76 | a0001c0001t0002g0004a0001c0001t0002g0118a0001c0001t0002g0128others(73): Show | 78 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(75): Show |
intron_variant | MODIFIER | c.108+4165_108+4176d others(14): Show |
MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr9 | 94379089 | |||||
| chr9:94379089
|
C | CTTTTTTT others(6): Show |
30 | a0001c0001t0002g0184a0001c0001t0002g0185a0001c0001t0002g0186others(27): Show | 30 | HG00597.hp2 HG00673.hp2 HG00741.hp2 others(27): Show |
intron_variant | MODIFIER | c.108+4164_108+4176d others(15): Show |
MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr9 | 94379089 | |||||
| chr9:94379089
|
C | CTTTTTTT others(7): Show |
7 | a0001c0001t0002g0198a0001c0001t0002g0218a0001c0001t0002g0219others(4): Show | 7 | HG02109.hp1 HG02135.hp1 HG02818.hp1 others(4): Show |
intron_variant | MODIFIER | c.108+4163_108+4176d others(16): Show |
MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr9 | 94379089 | |||||
| chr9:94379089
|
C | CTTTTTTT others(10): Show |
7 | a0001c0001t0007g0099a0001c0001t0007g0100a0001c0001t0007g0101others(4): Show | 7 | HG00544.hp1 HG01884.hp1 HG02895.hp1 others(4): Show |
intron_variant | MODIFIER | c.108+4176_108+4177i others(19): Show |
MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr9 | 94379089 | |||||
| chr9:94379089
|
C | CTTTTTTT others(11): Show |
2 | a0001c0001t0007g0105a0001c0001t0007g0106 | 2 | HG02630.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.108+4176_108+4177i others(20): Show |
MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr9 | 94379089 | |||||
| chr9:94379089
|
CTTTT | C | 32 | a0001c0001t0002g0315a0001c0001t0002g0316a0001c0001t0002g0317others(29): Show | 32 | HG00639.hp1 HG01109.hp2 HG01255.hp1 others(29): Show |
intron_variant | MODIFIER | c.108+4173_108+4176d others(6): Show |
MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr9 | 94379089 | |||||
| chr9:94379133
|
C | T | 1 | a0001c0001t0003g0183 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.108+4206C>T | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 1/11 | chr9 | 94379133 | ||||||
| chr9:94379138
|
G | A | 1 | a0001c0001t0001g0228 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.108+4211G>A | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 1/11 | chr9 | 94379138 | ||||||
| chr9:94379179
|
C | T | 11 | a0001c0001t0006g0107a0001c0001t0006g0108a0001c0001t0006g0109others(8): Show | 11 | HG01243.hp2 HG02109.hp1 HG02280.hp2 others(8): Show |
intron_variant | MODIFIER | c.108+4252C>T | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 1/11 | chr9 | 94379179 | ||||||
| chr9:94379180
|
G | A | 1 | a0001c0001t0015g0006 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.108+4253G>A | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 1/11 | chr9 | 94379180 | ||||||
| chr9:94379248
|
G | A | 89 | a0001c0001t0001g0001a0001c0001t0001g0225a0001c0001t0001g0226others(86): Show | 91 | HG00323.hp2 HG00408.hp2 HG00423.hp1 others(88): Show |
intron_variant | MODIFIER | c.108+4321G>A | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 1/11 | chr9 | 94379248 | ||||||
| chr9:94379297
|
G | A | 97 | a0001c0001t0002g0004a0001c0001t0002g0118a0001c0001t0002g0119others(94): Show | 99 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(96): Show |
intron_variant | MODIFIER | c.108+4370G>A | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 1/11 | chr9 | 94379297 | ||||||
| chr9:94379323
|
C | T | 97 | a0001c0001t0002g0004a0001c0001t0002g0118a0001c0001t0002g0119others(94): Show | 99 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(96): Show |
intron_variant | MODIFIER | c.108+4396C>T | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 1/11 | chr9 | 94379323 | ||||||
| chr9:94379386
|
C | CT | 14 | a0001c0001t0001g0080a0001c0001t0003g0196a0001c0001t0003g0208others(11): Show | 14 | HG00544.hp1 HG01358.hp1 HG01884.hp1 others(11): Show |
intron_variant | MODIFIER | c.108+4476dupT | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr9 | 94379386 | |||||
| chr9:94379386
|
CT | C | 22 | a0001c0001t0001g0003a0001c0001t0001g0081a0001c0001t0001g0082others(19): Show | 23 | HG00099.hp2 HG00280.hp2 HG00639.hp2 others(20): Show |
intron_variant | MODIFIER | c.108+4476delT | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr9 | 94379386 | |||||
| chr9:94379422
|
CTG | C | 97 | a0001c0001t0002g0004a0001c0001t0002g0118a0001c0001t0002g0119others(94): Show | 99 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(96): Show |
intron_variant | MODIFIER | c.108+4497_108+4498d others(4): Show |
MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr9 | 94379422 | |||||
| chr9:94379442
|
C | T | 1 | a0001c0001t0014g0227 | 1 | NA18992.hp2 | intron_variant | MODIFIER | c.108+4515C>T | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 1/11 | chr9 | 94379442 | ||||||
| chr9:94379443
|
G | A | 217 | a0001c0001t0002g0004a0001c0001t0002g0029a0001c0001t0002g0036others(214): Show | 220 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(217): Show |
intron_variant | MODIFIER | c.108+4516G>A | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 1/11 | chr9 | 94379443 | ||||||
| chr9:94379843
|
A | G | 1 | a0001c0001t0016g0025 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.108+4916A>G | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 1/11 | chr9 | 94379843 | ||||||
| chr9:94379868
|
C | T | 4 | a0001c0001t0005g0018a0001c0001t0005g0019a0001c0001t0005g0020others(1): Show | 4 | HG01081.hp2 HG01109.hp1 HG02486.hp2 others(1): Show |
intron_variant | MODIFIER | c.108+4941C>T | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 1/11 | chr9 | 94379868 | ||||||
| chr9:94379935
|
G | A | 1 | a0001c0001t0002g0128 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.108+5008G>A | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 1/11 | chr9 | 94379935 | ||||||
| chr9:94379962
|
G | C | 1 | a0001c0001t0013g0023 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.108+5035G>C | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 1/11 | chr9 | 94379962 | ||||||
| chr9:94379984
|
T | G | 2 | a0001c0001t0008g0009a0001c0001t0008g0010 | 2 | HG02818.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.108+5057T>G | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 1/11 | chr9 | 94379984 | ||||||
| chr9:94380184
|
G | A | 1 | a0001c0001t0002g0029 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.108+5257G>A | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 1/11 | chr9 | 94380184 | ||||||
| chr9:94380463
|
G | A | 1 | a0001c0001t0001g0230 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.108+5536G>A | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 1/11 | chr9 | 94380463 | ||||||
| chr9:94380551
|
G | A | 9 | a0001c0001t0007g0099a0001c0001t0007g0100a0001c0001t0007g0101others(6): Show | 9 | HG00544.hp1 HG01884.hp1 HG02630.hp1 others(6): Show |
intron_variant | MODIFIER | c.108+5624G>A | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 1/11 | chr9 | 94380551 | ||||||
| chr9:94380618
|
C | T | 1 | a0001c0001t0002g0339 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.108+5691C>T | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 1/11 | chr9 | 94380618 | ||||||
| chr9:94380696
|
C | A | 1 | a0001c0001t0001g0231 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.108+5769C>A | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 1/11 | chr9 | 94380696 | ||||||
| chr9:94380855
|
G | GTA | 217 | a0001c0001t0002g0004a0001c0001t0002g0029a0001c0001t0002g0036others(214): Show | 220 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(217): Show |
intron_variant | MODIFIER | c.108+5929_108+5930i others(4): Show |
MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr9 | 94380855 | |||||
| chr9:94381040
|
C | CT | 88 | a0001c0001t0001g0001a0001c0001t0001g0225a0001c0001t0001g0226others(85): Show | 90 | HG00323.hp2 HG00408.hp2 HG00423.hp1 others(87): Show |
intron_variant | MODIFIER | c.108+6126dupT | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr9 | 94381040 | |||||
| chr9:94381040
|
CT | C | 155 | a0001c0001t0002g0004a0001c0001t0002g0118a0001c0001t0002g0119others(152): Show | 157 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(154): Show |
intron_variant | MODIFIER | c.108+6126delT | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr9 | 94381040 | |||||
| chr9:94381248
|
C | A | 1 | a0001c0001t0017g0022 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.108+6321C>A | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 1/11 | chr9 | 94381248 | ||||||
| chr9:94381263
|
C | T | 97 | a0001c0001t0002g0004a0001c0001t0002g0118a0001c0001t0002g0119others(94): Show | 99 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(96): Show |
intron_variant | MODIFIER | c.108+6336C>T | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 1/11 | chr9 | 94381263 | ||||||
| chr9:94381352
|
C | CT | 6 | a0001c0001t0001g0001a0001c0001t0001g0307a0001c0001t0001g0309others(3): Show | 8 | NA18944.hp2 NA18950.hp1 NA18953.hp1 others(5): Show |
intron_variant | MODIFIER | c.108+6439dupT | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr9 | 94381352 | |||||
| chr9:94381361
|
T | G | 57 | a0001c0001t0002g0029a0001c0001t0002g0036a0001c0001t0002g0039others(54): Show | 58 | HG00597.hp1 HG00639.hp2 HG00642.hp1 others(55): Show |
intron_variant | MODIFIER | c.108+6434T>G | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 1/11 | chr9 | 94381361 | ||||||
| chr9:94381364
|
T | G | 59 | a0001c0001t0002g0029a0001c0001t0002g0036a0001c0001t0002g0039others(56): Show | 60 | HG00597.hp1 HG00639.hp2 HG00642.hp1 others(57): Show |
intron_variant | MODIFIER | c.108+6437T>G | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 1/11 | chr9 | 94381364 | ||||||
| chr9:94381446
|
T | TA | 57 | a0001c0001t0002g0029a0001c0001t0002g0036a0001c0001t0002g0039others(54): Show | 58 | HG00597.hp1 HG00639.hp2 HG00642.hp1 others(55): Show |
intron_variant | MODIFIER | c.108+6520dupA | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr9 | 94381446 | |||||
| chr9:94381459
|
A | G | 9 | a0001c0001t0007g0099a0001c0001t0007g0100a0001c0001t0007g0101others(6): Show | 9 | HG00544.hp1 HG01884.hp1 HG02630.hp1 others(6): Show |
intron_variant | MODIFIER | c.108+6532A>G | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 1/11 | chr9 | 94381459 | ||||||
| chr9:94381525
|
T | C | 57 | a0001c0001t0002g0029a0001c0001t0002g0036a0001c0001t0002g0039others(54): Show | 58 | HG00597.hp1 HG00639.hp2 HG00642.hp1 others(55): Show |
intron_variant | MODIFIER | c.108+6598T>C | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 1/11 | chr9 | 94381525 | ||||||
| chr9:94381615
|
A | G | 2 | a0001c0001t0002g0180a0001c0001t0003g0179 | 2 | HG00408.hp1 NA18974.hp2 |
intron_variant | MODIFIER | c.108+6688A>G | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 1/11 | chr9 | 94381615 | ||||||
| chr9:94381622
|
T | A | 7 | a0001c0001t0005g0002a0001c0001t0005g0030a0001c0001t0005g0031others(4): Show | 8 | HG01069.hp1 HG01071.hp1 HG02615.hp2 others(5): Show |
intron_variant | MODIFIER | c.108+6695T>A | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 1/11 | chr9 | 94381622 | ||||||
| chr9:94381701
|
T | C | 1 | a0001c0001t0017g0022 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.108+6774T>C | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 1/11 | chr9 | 94381701 | ||||||
| chr9:94381902
|
T | G | 1 | a0001c0001t0001g0082 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.108+6975T>G | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 1/11 | chr9 | 94381902 | ||||||
| chr9:94382037
|
T | C | 8 | a0001c0002t0009g0209a0001c0002t0009g0210a0001c0002t0009g0211others(5): Show | 8 | HG00140.hp2 HG00741.hp2 HG01255.hp2 others(5): Show |
intron_variant | MODIFIER | c.108+7110T>C | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 1/11 | chr9 | 94382037 | ||||||
| chr9:94382043
|
T | C | 2 | a0001c0001t0013g0023a0001c0001t0013g0024 | 2 | HG02040.hp2 HG02132.hp2 |
intron_variant | MODIFIER | c.108+7116T>C | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 1/11 | chr9 | 94382043 | ||||||
| chr9:94382045
|
C | T | 4 | a0001c0001t0001g0082a0001c0001t0001g0304a0001c0001t0001g0305others(1): Show | 4 | HG00733.hp2 HG02451.hp2 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.108+7118C>T | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 1/11 | chr9 | 94382045 | ||||||
| chr9:94382167
|
C | T | 1 | a0001c0003t0004g0068 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.108+7240C>T | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 1/11 | chr9 | 94382167 | ||||||
| chr9:94382172
|
A | G | 160 | a0001c0001t0002g0004a0001c0001t0002g0118a0001c0001t0002g0119others(157): Show | 162 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(159): Show |
intron_variant | MODIFIER | c.108+7245A>G | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 1/11 | chr9 | 94382172 | ||||||
| chr9:94382302
|
C | G | 4 | a0001c0001t0003g0176a0001c0001t0003g0177a0001c0001t0003g0178others(1): Show | 4 | HG00140.hp1 HG01074.hp2 HG02602.hp2 others(1): Show |
intron_variant | MODIFIER | c.108+7375C>G | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 1/11 | chr9 | 94382302 | ||||||
| chr9:94382333
|
A | G | 307 | a0001c0001t0001g0001a0001c0001t0001g0225a0001c0001t0001g0226others(304): Show | 312 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(309): Show |
intron_variant | MODIFIER | c.108+7406A>G | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 1/11 | chr9 | 94382333 | ||||||
| chr9:94382363
|
C | T | 1 | a0001c0001t0003g0175 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.108+7436C>T | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 1/11 | chr9 | 94382363 | ||||||
| chr9:94382390
|
A | G | 1 | a0001c0001t0002g0316 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.108+7463A>G | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 1/11 | chr9 | 94382390 | ||||||
| chr9:94382471
|
T | C | 1 | a0001c0001t0003g0129 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.108+7544T>C | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 1/11 | chr9 | 94382471 | ||||||
| chr9:94382718
|
G | A | 9 | a0001c0001t0007g0099a0001c0001t0007g0100a0001c0001t0007g0101others(6): Show | 9 | HG00544.hp1 HG01884.hp1 HG02630.hp1 others(6): Show |
intron_variant | MODIFIER | c.108+7791G>A | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 1/11 | chr9 | 94382718 | ||||||
| chr9:94382897
|
G | A | 1 | a0001c0001t0004g0035 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.108+7970G>A | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 1/11 | chr9 | 94382897 | ||||||
| chr9:94382906
|
G | A | 10 | a0001c0001t0001g0226a0001c0001t0001g0232a0001c0001t0001g0233others(7): Show | 10 | HG01069.hp2 HG01099.hp1 HG01167.hp2 others(7): Show |
intron_variant | MODIFIER | c.108+7979G>A | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 1/11 | chr9 | 94382906 | ||||||
| chr9:94383096
|
T | C | 10 | a0001c0001t0008g0009a0001c0001t0008g0010a0001c0001t0008g0011others(7): Show | 10 | HG01081.hp1 HG02280.hp1 HG02559.hp1 others(7): Show |
intron_variant | MODIFIER | c.108+8169T>C | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 1/11 | chr9 | 94383096 | ||||||
| chr9:94383161
|
C | CT | 59 | a0001c0001t0001g0226a0001c0001t0001g0240a0001c0001t0002g0029others(56): Show | 60 | HG00597.hp1 HG00639.hp2 HG00642.hp1 others(57): Show |
intron_variant | MODIFIER | c.108+8253dupT | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr9 | 94383161 | |||||
| chr9:94383161
|
C | CTT | 43 | a0001c0001t0002g0130a0001c0001t0002g0131a0001c0001t0002g0132others(40): Show | 43 | HG00140.hp2 HG00280.hp1 HG00544.hp1 others(40): Show |
intron_variant | MODIFIER | c.108+8252_108+8253d others(4): Show |
MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr9 | 94383161 | |||||
| chr9:94383161
|
C | CTTT | 112 | a0001c0001t0002g0004a0001c0001t0002g0118a0001c0001t0002g0119others(109): Show | 114 | HG00099.hp1 HG00140.hp1 HG00408.hp1 others(111): Show |
intron_variant | MODIFIER | c.108+8251_108+8253d others(5): Show |
MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr9 | 94383161 | |||||
| chr9:94383161
|
C | CTTTT | 6 | a0001c0001t0002g0194a0001c0001t0002g0335a0001c0001t0003g0173others(3): Show | 6 | HG02027.hp2 HG02074.hp1 NA18955.hp2 others(3): Show |
intron_variant | MODIFIER | c.108+8250_108+8253d others(6): Show |
MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr9 | 94383161 | |||||
| chr9:94383277
|
C | T | 2 | a0001c0001t0003g0007a0001c0001t0003g0008 | 2 | HG02615.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.108+8350C>T | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 1/11 | chr9 | 94383277 | ||||||
| chr9:94383370
|
C | T | 1 | a0001c0001t0004g0066 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.108+8443C>T | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 1/11 | chr9 | 94383370 | ||||||
| chr9:94383451
|
A | G | 160 | a0001c0001t0002g0004a0001c0001t0002g0118a0001c0001t0002g0119others(157): Show | 162 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(159): Show |
intron_variant | MODIFIER | c.108+8524A>G | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 1/11 | chr9 | 94383451 | ||||||
| chr9:94383496
|
A | G | 1 | a0001c0001t0001g0303 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.108+8569A>G | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 1/11 | chr9 | 94383496 | ||||||
| chr9:94383643
|
A | G | 57 | a0001c0001t0002g0029a0001c0001t0002g0036a0001c0001t0002g0039others(54): Show | 58 | HG00597.hp1 HG00639.hp2 HG00642.hp1 others(55): Show |
intron_variant | MODIFIER | c.108+8716A>G | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 1/11 | chr9 | 94383643 | ||||||
| chr9:94383754
|
A | C | 1 | a0001c0001t0017g0022 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.108+8827A>C | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 1/11 | chr9 | 94383754 | ||||||
| chr9:94383929
|
A | G | 2 | a0001c0001t0005g0033a0001c0001t0005g0034 | 2 | HG03195.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.108+9002A>G | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 1/11 | chr9 | 94383929 | ||||||
| chr9:94384133
|
C | T | 1 | a0001c0001t0017g0022 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.108+9206C>T | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 1/11 | chr9 | 94384133 | ||||||
| chr9:94384182
|
A | G | 3 | a0001c0001t0002g0218a0001c0001t0002g0219a0001c0001t0002g0220 | 3 | HG02818.hp1 HG03209.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.108+9255A>G | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 1/11 | chr9 | 94384182 | ||||||
| chr9:94384336
|
C | CT | 66 | a0001c0001t0001g0309a0001c0001t0002g0153a0001c0001t0002g0180others(63): Show | 67 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(64): Show |
intron_variant | MODIFIER | c.108+9426dupT | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr9 | 94384336 | |||||
| chr9:94384478
|
T | C | 2 | a0001c0001t0001g0225a0001c0001t0001g0241 | 2 | HG03491.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.108+9551T>C | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 1/11 | chr9 | 94384478 | ||||||
| chr9:94384581
|
A | G | 1 | a0001c0001t0015g0006 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.108+9654A>G | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 1/11 | chr9 | 94384581 | ||||||
| chr9:94384615
|
C | G | 2 | a0001c0001t0001g0310a0001c0001t0001g0311 | 2 | HG02258.hp1 HG02622.hp1 |
intron_variant | MODIFIER | c.108+9688C>G | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 1/11 | chr9 | 94384615 | ||||||
| chr9:94384620
|
A | G | 1 | a0001c0001t0002g0334 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.108+9693A>G | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 1/11 | chr9 | 94384620 | ||||||
| chr9:94384670
|
C | T | 1 | a0001c0001t0008g0012 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.108+9743C>T | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 1/11 | chr9 | 94384670 | ||||||
| chr9:94384700
|
C | A | 160 | a0001c0001t0002g0004a0001c0001t0002g0118a0001c0001t0002g0119others(157): Show | 162 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(159): Show |
intron_variant | MODIFIER | c.108+9773C>A | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 1/11 | chr9 | 94384700 | ||||||
| chr9:94384744
|
A | C | 57 | a0001c0001t0002g0029a0001c0001t0002g0036a0001c0001t0002g0039others(54): Show | 58 | HG00597.hp1 HG00639.hp2 HG00642.hp1 others(55): Show |
intron_variant | MODIFIER | c.108+9817A>C | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 1/11 | chr9 | 94384744 | ||||||
| chr9:94384786
|
G | T | 1 | a0001c0001t0008g0016 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.108+9859G>T | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 1/11 | chr9 | 94384786 | ||||||
| chr9:94384933
|
A | G | 1 | a0001c0001t0003g0202 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.108+10006A>G | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 1/11 | chr9 | 94384933 | ||||||
| chr9:94384981
|
C | G | 1 | a0001c0001t0003g0172 | 1 | NA18957.hp1 | intron_variant | MODIFIER | c.108+10054C>G | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 1/11 | chr9 | 94384981 | ||||||
| chr9:94385375
|
G | A | 1 | a0001c0001t0002g0317 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.108+10448G>A | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 1/11 | chr9 | 94385375 | ||||||
| chr9:94385548
|
A | G | 1 | a0001c0001t0003g0171 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.108+10621A>G | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 1/11 | chr9 | 94385548 | ||||||
| chr9:94385558
|
G | A | 3 | a0001c0001t0002g0218a0001c0001t0002g0219a0001c0001t0002g0220 | 3 | HG02818.hp1 HG03209.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.108+10631G>A | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 1/11 | chr9 | 94385558 | ||||||
| chr9:94385569
|
G | A | 160 | a0001c0001t0002g0004a0001c0001t0002g0118a0001c0001t0002g0119others(157): Show | 162 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(159): Show |
intron_variant | MODIFIER | c.108+10642G>A | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 1/11 | chr9 | 94385569 | ||||||
| chr9:94385716
|
C | T | 1 | a0001c0001t0001g0302 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.108+10789C>T | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 1/11 | chr9 | 94385716 | ||||||
| chr9:94385750
|
G | A | 218 | a0001c0001t0002g0004a0001c0001t0002g0029a0001c0001t0002g0036others(215): Show | 221 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(218): Show |
intron_variant | MODIFIER | c.108+10823G>A | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 1/11 | chr9 | 94385750 | ||||||
| chr9:94385859
|
C | A | 1 | a0001c0001t0001g0097 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.108+10932C>A | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 1/11 | chr9 | 94385859 | ||||||
| chr9:94386246
|
T | G | 19 | a0001c0001t0001g0003a0001c0001t0001g0081a0001c0001t0001g0082others(16): Show | 20 | HG00099.hp2 HG00280.hp2 HG00642.hp2 others(17): Show |
intron_variant | MODIFIER | c.108+11319T>G | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 1/11 | chr9 | 94386246 | ||||||
| chr9:94386266
|
T | A | 1 | a0001c0001t0002g0340 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.108+11339T>A | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 1/11 | chr9 | 94386266 | ||||||
| chr9:94386267
|
C | CAT | 250 | a0001c0001t0001g0003a0001c0001t0001g0081a0001c0001t0001g0082others(247): Show | 254 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(251): Show |
intron_variant | MODIFIER | c.108+11340_108+1134 others(6): Show |
MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 1/11 | chr9 | 94386267 | ||||||
| chr9:94386407
|
G | A | 11 | a0001c0001t0006g0107a0001c0001t0006g0108a0001c0001t0006g0109others(8): Show | 11 | HG01243.hp2 HG02109.hp1 HG02280.hp2 others(8): Show |
intron_variant | MODIFIER | c.108+11480G>A | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 1/11 | chr9 | 94386407 | ||||||
| chr9:94386481
|
G | GT | 4 | a0001c0001t0002g0148a0001c0001t0002g0149a0001c0001t0002g0150others(1): Show | 4 | HG00741.hp1 NA18944.hp1 NA19000.hp1 others(1): Show |
intron_variant | MODIFIER | c.108+11556dupT | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr9 | 94386481 | |||||
| chr9:94386536
|
A | G | 8 | a0001c0002t0009g0209a0001c0002t0009g0210a0001c0002t0009g0211others(5): Show | 8 | HG00140.hp2 HG00741.hp2 HG01255.hp2 others(5): Show |
intron_variant | MODIFIER | c.108+11609A>G | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 1/11 | chr9 | 94386536 | ||||||
| chr9:94386564
|
C | G | 159 | a0001c0001t0002g0004a0001c0001t0002g0118a0001c0001t0002g0119others(156): Show | 161 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(158): Show |
intron_variant | MODIFIER | c.108+11637C>G | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 1/11 | chr9 | 94386564 | ||||||
| chr9:94386652
|
A | G | 89 | a0001c0001t0001g0001a0001c0001t0001g0225a0001c0001t0001g0226others(86): Show | 91 | HG00323.hp2 HG00408.hp2 HG00423.hp1 others(88): Show |
intron_variant | MODIFIER | c.108+11725A>G | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 1/11 | chr9 | 94386652 | ||||||
| chr9:94387032
|
A | G | 1 | a0001c0001t0017g0022 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.108+12105A>G | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 1/11 | chr9 | 94387032 | ||||||
| chr9:94387066
|
C | T | 1 | a0001c0001t0016g0025 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.108+12139C>T | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 1/11 | chr9 | 94387066 | ||||||
| chr9:94387080
|
T | G | 57 | a0001c0001t0002g0029a0001c0001t0002g0036a0001c0001t0002g0039others(54): Show | 58 | HG00597.hp1 HG00639.hp2 HG00642.hp1 others(55): Show |
intron_variant | MODIFIER | c.108+12153T>G | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 1/11 | chr9 | 94387080 | ||||||
| chr9:94387081
|
C | T | 2 | a0001c0001t0002g0188a0001c0001t0002g0198 | 2 | NA18967.hp1 NA18994.hp2 |
intron_variant | MODIFIER | c.108+12154C>T | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 1/11 | chr9 | 94387081 | ||||||
| chr9:94387151
|
A | G | 11 | a0001c0001t0006g0107a0001c0001t0006g0108a0001c0001t0006g0109others(8): Show | 11 | HG01243.hp2 HG02109.hp1 HG02280.hp2 others(8): Show |
intron_variant | MODIFIER | c.108+12224A>G | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 1/11 | chr9 | 94387151 | ||||||
| chr9:94387281
|
G | C | 160 | a0001c0001t0002g0004a0001c0001t0002g0118a0001c0001t0002g0119others(157): Show | 162 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(159): Show |
intron_variant | MODIFIER | c.108+12354G>C | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 1/11 | chr9 | 94387281 | ||||||
| chr9:94387427
|
A | AT | 58 | a0001c0001t0002g0029a0001c0001t0002g0036a0001c0001t0002g0039others(55): Show | 59 | HG00597.hp1 HG00639.hp2 HG00642.hp1 others(56): Show |
intron_variant | MODIFIER | c.108+12510dupT | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr9 | 94387427 | |||||
| chr9:94387427
|
AT | A | 14 | a0001c0001t0002g0123a0001c0001t0003g0133a0001c0001t0003g0152others(11): Show | 14 | HG01081.hp1 HG01192.hp1 HG01516.hp2 others(11): Show |
intron_variant | MODIFIER | c.108+12510delT | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr9 | 94387427 | |||||
| chr9:94387628
|
G | C | 14 | a0001c0001t0001g0242a0001c0001t0001g0243a0001c0001t0001g0244others(11): Show | 14 | HG00423.hp1 HG03239.hp2 NA18612.hp1 others(11): Show |
intron_variant | MODIFIER | c.108+12701G>C | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 1/11 | chr9 | 94387628 | ||||||
| chr9:94387880
|
G | A | 1 | a0001c0001t0002g0340 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.108+12953G>A | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 1/11 | chr9 | 94387880 | ||||||
| chr9:94387923
|
T | C | 4 | a0001c0001t0008g0009a0001c0001t0008g0010a0001c0001t0008g0011others(1): Show | 4 | HG02818.hp2 HG02922.hp2 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.108+12996T>C | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 1/11 | chr9 | 94387923 | ||||||
| chr9:94388066
|
A | G | 37 | a0001c0001t0004g0027a0001c0001t0004g0028a0001c0001t0004g0042others(34): Show | 37 | HG00597.hp1 HG00639.hp2 HG00642.hp1 others(34): Show |
intron_variant | MODIFIER | c.108+13139A>G | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 1/11 | chr9 | 94388066 | ||||||
| chr9:94388122
|
G | A | 2 | a0001c0001t0002g0029a0001c0001t0002g0036 | 2 | HG01243.hp1 HG02572.hp1 |
intron_variant | MODIFIER | c.108+13195G>A | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 1/11 | chr9 | 94388122 | ||||||
| chr9:94388141
|
A | AG | 218 | a0001c0001t0002g0004a0001c0001t0002g0029a0001c0001t0002g0036others(215): Show | 221 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(218): Show |
intron_variant | MODIFIER | c.108+13214_108+1321 others(5): Show |
MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 1/11 | chr9 | 94388141 | ||||||
| chr9:94388206
|
GAAAAAAG others(6): Show |
G | 4 | a0001c0001t0003g0168a0001c0001t0003g0169a0001c0001t0003g0170others(1): Show | 4 | HG02698.hp2 HG02738.hp1 HG03688.hp2 others(1): Show |
intron_variant | MODIFIER | c.108+13284_108+1329 others(17): Show |
MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr9 | 94388206 | |||||
| chr9:94388321
|
A | T | 160 | a0001c0001t0002g0004a0001c0001t0002g0118a0001c0001t0002g0119others(157): Show | 162 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(159): Show |
intron_variant | MODIFIER | c.108+13394A>T | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 1/11 | chr9 | 94388321 | ||||||
| chr9:94388340
|
T | G | 49 | a0001c0001t0002g0315a0001c0001t0002g0316a0001c0001t0002g0317others(46): Show | 49 | HG00140.hp2 HG00544.hp1 HG00639.hp1 others(46): Show |
intron_variant | MODIFIER | c.108+13413T>G | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 1/11 | chr9 | 94388340 | ||||||
| chr9:94388373
|
G | A | 1 | a0001c0001t0001g0082 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.108+13446G>A | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 1/11 | chr9 | 94388373 | ||||||
| chr9:94388804
|
A | G | 3 | a0001c0001t0001g0304a0001c0001t0001g0305a0001c0001t0001g0306 | 3 | HG02451.hp2 HG03471.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.108+13877A>G | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 1/11 | chr9 | 94388804 | ||||||
| chr9:94388912
|
C | T | 218 | a0001c0001t0002g0004a0001c0001t0002g0029a0001c0001t0002g0036others(215): Show | 221 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(218): Show |
intron_variant | MODIFIER | c.108+13985C>T | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 1/11 | chr9 | 94388912 | ||||||
| chr9:94388961
|
C | T | 3 | a0001c0001t0002g0218a0001c0001t0002g0219a0001c0001t0002g0220 | 3 | HG02818.hp1 HG03209.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.108+14034C>T | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 1/11 | chr9 | 94388961 | ||||||
| chr9:94388974
|
A | C | 3 | a0001c0001t0002g0340a0001c0001t0002g0341a0001c0001t0002g0342 | 3 | HG01884.hp2 HG02886.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.108+14047A>C | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 1/11 | chr9 | 94388974 | ||||||
| chr9:94389059
|
G | A | 1 | a0001c0001t0002g0318 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.108+14132G>A | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 1/11 | chr9 | 94389059 | ||||||
| chr9:94389134
|
ATAGT | A | 3 | a0001c0001t0002g0340a0001c0001t0002g0341a0001c0001t0002g0342 | 3 | HG01884.hp2 HG02886.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.108+14211_108+1421 others(8): Show |
MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr9 | 94389134 | |||||
| chr9:94389203
|
A | G | 1 | a0001c0001t0003g0221 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.108+14276A>G | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 1/11 | chr9 | 94389203 | ||||||
| chr9:94389271
|
G | GT | 67 | a0001c0001t0001g0301a0001c0001t0002g0029a0001c0001t0002g0036others(64): Show | 68 | HG00544.hp1 HG00597.hp1 HG00639.hp2 others(65): Show |
intron_variant | MODIFIER | c.108+14356dupT | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr9 | 94389271 | |||||
| chr9:94389450
|
A | T | 54 | a0001c0001t0002g0029a0001c0001t0002g0036a0001c0001t0002g0039others(51): Show | 55 | HG00323.hp2 HG00597.hp1 HG00639.hp2 others(52): Show |
intron_variant | MODIFIER | c.108+14523A>T | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 1/11 | chr9 | 94389450 | ||||||
| chr9:94389452
|
T | A | 8 | a0001c0002t0009g0209a0001c0002t0009g0210a0001c0002t0009g0211others(5): Show | 8 | HG00140.hp2 HG00741.hp2 HG01255.hp2 others(5): Show |
intron_variant | MODIFIER | c.108+14525T>A | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 1/11 | chr9 | 94389452 | ||||||
| chr9:94389525
|
C | T | 1 | a0001c0001t0016g0025 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.108+14598C>T | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 1/11 | chr9 | 94389525 | ||||||
| chr9:94389526
|
G | A | 160 | a0001c0001t0002g0004a0001c0001t0002g0118a0001c0001t0002g0119others(157): Show | 162 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(159): Show |
intron_variant | MODIFIER | c.108+14599G>A | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 1/11 | chr9 | 94389526 | ||||||
| chr9:94389669
|
C | T | 1 | a0002c0004t0001g0299 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.108+14742C>T | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 1/11 | chr9 | 94389669 | ||||||
| chr9:94389714
|
C | T | 89 | a0001c0001t0001g0001a0001c0001t0001g0225a0001c0001t0001g0226others(86): Show | 91 | HG00323.hp2 HG00408.hp2 HG00423.hp1 others(88): Show |
intron_variant | MODIFIER | c.108+14787C>T | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 1/11 | chr9 | 94389714 | ||||||
| chr9:94389791
|
A | G | 1 | a0001c0001t0004g0067 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.108+14864A>G | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 1/11 | chr9 | 94389791 | ||||||
| chr9:94389799
|
G | T | 160 | a0001c0001t0002g0004a0001c0001t0002g0118a0001c0001t0002g0119others(157): Show | 162 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(159): Show |
intron_variant | MODIFIER | c.108+14872G>T | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 1/11 | chr9 | 94389799 | ||||||
| chr9:94389923
|
A | G | 9 | a0001c0001t0007g0099a0001c0001t0007g0100a0001c0001t0007g0101others(6): Show | 9 | HG00544.hp1 HG01884.hp1 HG02630.hp1 others(6): Show |
intron_variant | MODIFIER | c.108+14996A>G | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 1/11 | chr9 | 94389923 | ||||||
| chr9:94390028
|
C | T | 11 | a0001c0001t0006g0107a0001c0001t0006g0108a0001c0001t0006g0109others(8): Show | 11 | HG01243.hp2 HG02109.hp1 HG02280.hp2 others(8): Show |
intron_variant | MODIFIER | c.108+15101C>T | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 1/11 | chr9 | 94390028 | ||||||
| chr9:94390082
|
C | T | 1 | a0001c0001t0002g0333 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.108+15155C>T | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 1/11 | chr9 | 94390082 | ||||||
| chr9:94390093
|
A | G | 1 | a0001c0001t0001g0301 | 1 | NA18972.hp2 | intron_variant | MODIFIER | c.108+15166A>G | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 1/11 | chr9 | 94390093 | ||||||
| chr9:94390103
|
A | G | 49 | a0001c0001t0002g0315a0001c0001t0002g0316a0001c0001t0002g0317others(46): Show | 49 | HG00140.hp2 HG00544.hp1 HG00639.hp1 others(46): Show |
intron_variant | MODIFIER | c.108+15176A>G | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 1/11 | chr9 | 94390103 | ||||||
| chr9:94390123
|
A | G | 8 | a0001c0002t0009g0209a0001c0002t0009g0210a0001c0002t0009g0211others(5): Show | 8 | HG00140.hp2 HG00741.hp2 HG01255.hp2 others(5): Show |
intron_variant | MODIFIER | c.108+15196A>G | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 1/11 | chr9 | 94390123 | ||||||
| chr9:94390136
|
C | T | 1 | a0001c0001t0017g0022 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.108+15209C>T | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 1/11 | chr9 | 94390136 | ||||||
| chr9:94390169
|
G | A | 97 | a0001c0001t0002g0004a0001c0001t0002g0118a0001c0001t0002g0119others(94): Show | 99 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(96): Show |
intron_variant | MODIFIER | c.108+15242G>A | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 1/11 | chr9 | 94390169 | ||||||
| chr9:94390171
|
G | C | 1 | a0001c0001t0001g0242 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.108+15244G>C | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 1/11 | chr9 | 94390171 | ||||||
| chr9:94390180
|
T | C | 160 | a0001c0001t0002g0004a0001c0001t0002g0118a0001c0001t0002g0119others(157): Show | 162 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(159): Show |
intron_variant | MODIFIER | c.108+15253T>C | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 1/11 | chr9 | 94390180 | ||||||
| chr9:94390275
|
A | G | 218 | a0001c0001t0002g0004a0001c0001t0002g0029a0001c0001t0002g0036others(215): Show | 221 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(218): Show |
intron_variant | MODIFIER | c.108+15348A>G | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 1/11 | chr9 | 94390275 | ||||||
| chr9:94390322
|
T | G | 1 | a0001c0001t0017g0022 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.108+15395T>G | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 1/11 | chr9 | 94390322 | ||||||
| chr9:94390350
|
G | A | 218 | a0001c0001t0002g0004a0001c0001t0002g0029a0001c0001t0002g0036others(215): Show | 221 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(218): Show |
intron_variant | MODIFIER | c.108+15423G>A | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 1/11 | chr9 | 94390350 | ||||||
| chr9:94390371
|
G | C | 1 | a0001c0001t0002g0004 | 2 | HG02083.hp2 NA19080.hp2 |
intron_variant | MODIFIER | c.108+15444G>C | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 1/11 | chr9 | 94390371 | ||||||
| chr9:94390505
|
C | T | 3 | a0001c0001t0002g0218a0001c0001t0002g0219a0001c0001t0002g0220 | 3 | HG02818.hp1 HG03209.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.108+15578C>T | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 1/11 | chr9 | 94390505 | ||||||
| chr9:94390515
|
ACAGTCC | A | 4 | a0001c0001t0003g0168a0001c0001t0003g0169a0001c0001t0003g0170others(1): Show | 4 | HG02698.hp2 HG02738.hp1 HG03688.hp2 others(1): Show |
intron_variant | MODIFIER | c.108+15589_108+1559 others(10): Show |
MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 1/11 | chr9 | 94390515 | ||||||
| chr9:94390525
|
C | T | 1 | a0001c0001t0008g0011 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.108+15598C>T | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 1/11 | chr9 | 94390525 | ||||||
| chr9:94390553
|
G | T | 160 | a0001c0001t0002g0004a0001c0001t0002g0118a0001c0001t0002g0119others(157): Show | 162 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(159): Show |
intron_variant | MODIFIER | c.108+15626G>T | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 1/11 | chr9 | 94390553 | ||||||
| chr9:94390628
|
A | G | 2 | a0001c0001t0008g0009a0001c0001t0008g0010 | 2 | HG02818.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.108+15701A>G | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 1/11 | chr9 | 94390628 | ||||||
| chr9:94390804
|
A | T | 160 | a0001c0001t0002g0004a0001c0001t0002g0118a0001c0001t0002g0119others(157): Show | 162 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(159): Show |
intron_variant | MODIFIER | c.108+15877A>T | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 1/11 | chr9 | 94390804 | ||||||
| chr9:94390843
|
G | A | 1 | a0001c0001t0018g0041 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.108+15916G>A | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 1/11 | chr9 | 94390843 | ||||||
| chr9:94391076
|
G | A | 1 | a0001c0001t0003g0168 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.108+16149G>A | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 1/11 | chr9 | 94391076 | ||||||
| chr9:94391197
|
C | CA | 13 | a0001c0001t0002g0148a0001c0001t0002g0316a0001c0001t0002g0318others(10): Show | 13 | HG00741.hp1 HG01243.hp2 HG01952.hp1 others(10): Show |
intron_variant | MODIFIER | c.108+16292dupA | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr9 | 94391197 | |||||
| chr9:94391197
|
CA | C | 14 | a0001c0001t0001g0225a0001c0001t0001g0239a0001c0001t0001g0298others(11): Show | 14 | HG01069.hp2 HG01255.hp1 HG01517.hp1 others(11): Show |
intron_variant | MODIFIER | c.108+16292delA | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr9 | 94391197 | |||||
| chr9:94391234
|
C | T | 5 | a0001c0001t0001g0294a0001c0001t0001g0295a0001c0001t0001g0296others(2): Show | 5 | HG02572.hp2 HG02717.hp1 HG02970.hp2 others(2): Show |
intron_variant | MODIFIER | c.108+16307C>T | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 1/11 | chr9 | 94391234 | ||||||
| chr9:94391323
|
A | G | 1 | a0001c0001t0004g0065 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.108+16396A>G | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 1/11 | chr9 | 94391323 | ||||||
| chr9:94391362
|
TA | T | 9 | a0001c0001t0001g0294a0001c0001t0001g0295a0001c0001t0001g0296others(6): Show | 9 | HG02040.hp2 HG02132.hp2 HG02572.hp2 others(6): Show |
intron_variant | MODIFIER | c.108+16450delA | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr9 | 94391362 | |||||
| chr9:94391377
|
A | C | 1 | a0001c0001t0007g0102 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.108+16450A>C | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 1/11 | chr9 | 94391377 | ||||||
| chr9:94391413
|
G | A | 1 | a0001c0001t0002g0320 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.108+16486G>A | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 1/11 | chr9 | 94391413 | ||||||
| chr9:94391590
|
C | T | 2 | a0001c0001t0013g0023a0001c0001t0013g0024 | 2 | HG02040.hp2 HG02132.hp2 |
intron_variant | MODIFIER | c.108+16663C>T | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 1/11 | chr9 | 94391590 | ||||||
| chr9:94391651
|
G | T | 1 | a0001c0001t0004g0043 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.108+16724G>T | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 1/11 | chr9 | 94391651 | ||||||
| chr9:94391652
|
T | C | 160 | a0001c0001t0002g0004a0001c0001t0002g0118a0001c0001t0002g0119others(157): Show | 162 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(159): Show |
intron_variant | MODIFIER | c.108+16725T>C | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 1/11 | chr9 | 94391652 | ||||||
| chr9:94391714
|
T | C | 1 | a0001c0001t0002g0320 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.108+16787T>C | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 1/11 | chr9 | 94391714 | ||||||
| chr9:94391741
|
C | T | 341 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0079others(338): Show | 347 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(344): Show |
intron_variant | MODIFIER | c.108+16814C>T | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 1/11 | chr9 | 94391741 | ||||||
| chr9:94391748
|
G | A | 2 | a0001c0001t0007g0100a0001c0001t0007g0105 | 2 | HG02922.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.108+16821G>A | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 1/11 | chr9 | 94391748 | ||||||
| chr9:94391847
|
C | G | 7 | a0001c0001t0001g0242a0001c0001t0001g0250a0001c0001t0001g0251others(4): Show | 7 | HG00423.hp1 NA18953.hp2 NA18959.hp1 others(4): Show |
intron_variant | MODIFIER | c.108+16920C>G | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 1/11 | chr9 | 94391847 | ||||||
| chr9:94391888
|
T | A | 59 | a0001c0001t0002g0315a0001c0001t0002g0316a0001c0001t0002g0317others(56): Show | 59 | HG00140.hp2 HG00544.hp1 HG00639.hp1 others(56): Show |
intron_variant | MODIFIER | c.108+16961T>A | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 1/11 | chr9 | 94391888 | ||||||
| chr9:94392009
|
C | T | 3 | a0001c0001t0003g0192a0001c0001t0003g0193a0001c0001t0003g0197 | 3 | HG00597.hp2 HG00673.hp2 HG02135.hp1 |
intron_variant | MODIFIER | c.108+17082C>T | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 1/11 | chr9 | 94392009 | ||||||
| chr9:94392025
|
C | T | 19 | a0001c0001t0001g0003a0001c0001t0001g0081a0001c0001t0001g0082others(16): Show | 20 | HG00099.hp2 HG00280.hp2 HG00642.hp2 others(17): Show |
intron_variant | MODIFIER | c.108+17098C>T | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 1/11 | chr9 | 94392025 | ||||||
| chr9:94392125
|
G | C | 7 | a0001c0001t0007g0099a0001c0001t0007g0100a0001c0001t0007g0101others(4): Show | 7 | HG01884.hp1 HG02630.hp1 HG02895.hp1 others(4): Show |
intron_variant | MODIFIER | c.108+17198G>C | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 1/11 | chr9 | 94392125 | ||||||
| chr9:94392244
|
T | C | 1 | a0001c0001t0002g0029 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.108+17317T>C | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 1/11 | chr9 | 94392244 | ||||||
| chr9:94392444
|
G | A | 307 | a0001c0001t0001g0001a0001c0001t0001g0225a0001c0001t0001g0226others(304): Show | 312 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(309): Show |
intron_variant | MODIFIER | c.108+17517G>A | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 1/11 | chr9 | 94392444 | ||||||
| chr9:94392469
|
G | T | 1 | a0001c0001t0017g0022 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.108+17542G>T | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 1/11 | chr9 | 94392469 | ||||||
| chr9:94392506
|
AT | A | 160 | a0001c0001t0001g0257a0001c0001t0002g0004a0001c0001t0002g0118others(157): Show | 162 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(159): Show |
intron_variant | MODIFIER | c.108+17592delT | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr9 | 94392506 | |||||
| chr9:94392586
|
C | T | 1 | a0001c0001t0001g0306 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.108+17659C>T | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 1/11 | chr9 | 94392586 | ||||||
| chr9:94392619
|
G | A | 2 | a0001c0001t0002g0321a0001c0001t0002g0322 | 2 | HG00639.hp1 HG01109.hp2 |
intron_variant | MODIFIER | c.108+17692G>A | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 1/11 | chr9 | 94392619 | ||||||
| chr9:94392756
|
C | T | 57 | a0001c0001t0002g0029a0001c0001t0002g0036a0001c0001t0002g0039others(54): Show | 58 | HG00597.hp1 HG00639.hp2 HG00642.hp1 others(55): Show |
intron_variant | MODIFIER | c.108+17829C>T | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 1/11 | chr9 | 94392756 | ||||||
| chr9:94392794
|
C | T | 1 | a0001c0001t0001g0293 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.108+17867C>T | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 1/11 | chr9 | 94392794 | ||||||
| chr9:94392830
|
GATC | G | 89 | a0001c0001t0001g0001a0001c0001t0001g0225a0001c0001t0001g0226others(86): Show | 91 | HG00323.hp2 HG00408.hp2 HG00423.hp1 others(88): Show |
intron_variant | MODIFIER | c.108+17907_108+1790 others(7): Show |
MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr9 | 94392830 | |||||
| chr9:94392843
|
A | G | 11 | a0001c0001t0006g0107a0001c0001t0006g0108a0001c0001t0006g0109others(8): Show | 11 | HG01243.hp2 HG02109.hp1 HG02280.hp2 others(8): Show |
intron_variant | MODIFIER | c.108+17916A>G | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 1/11 | chr9 | 94392843 | ||||||
| chr9:94392971
|
A | T | 57 | a0001c0001t0002g0029a0001c0001t0002g0036a0001c0001t0002g0039others(54): Show | 58 | HG00597.hp1 HG00639.hp2 HG00642.hp1 others(55): Show |
intron_variant | MODIFIER | c.108+18044A>T | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 1/11 | chr9 | 94392971 | ||||||
| chr9:94393068
|
G | A | 1 | a0001c0001t0001g0310 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.108+18141G>A | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 1/11 | chr9 | 94393068 | ||||||
| chr9:94393353
|
G | C | 1 | a0001c0001t0002g0340 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.108+18426G>C | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 1/11 | chr9 | 94393353 | ||||||
| chr9:94393442
|
G | A | 2 | a0001c0001t0004g0035a0001c0001t0004g0037 | 2 | HG02896.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.108+18515G>A | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 1/11 | chr9 | 94393442 | ||||||
| chr9:94393452
|
A | G | 1 | a0001c0001t0017g0022 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.108+18525A>G | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 1/11 | chr9 | 94393452 | ||||||
| chr9:94393550
|
T | C | 8 | a0001c0002t0009g0209a0001c0002t0009g0210a0001c0002t0009g0211others(5): Show | 8 | HG00140.hp2 HG00741.hp2 HG01255.hp2 others(5): Show |
intron_variant | MODIFIER | c.108+18623T>C | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 1/11 | chr9 | 94393550 | ||||||
| chr9:94393658
|
G | C | 10 | a0001c0001t0001g0228a0001c0001t0001g0231a0001c0001t0001g0258others(7): Show | 10 | HG00621.hp1 HG01261.hp1 HG02015.hp2 others(7): Show |
intron_variant | MODIFIER | c.108+18731G>C | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 1/11 | chr9 | 94393658 | ||||||
| chr9:94393823
|
G | A | 160 | a0001c0001t0002g0004a0001c0001t0002g0118a0001c0001t0002g0119others(157): Show | 162 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(159): Show |
intron_variant | MODIFIER | c.108+18896G>A | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 1/11 | chr9 | 94393823 | ||||||
| chr9:94393860
|
G | A | 5 | a0001c0001t0008g0013a0001c0001t0008g0014a0001c0001t0008g0015others(2): Show | 5 | HG01081.hp1 HG02280.hp1 HG02559.hp1 others(2): Show |
intron_variant | MODIFIER | c.108+18933G>A | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 1/11 | chr9 | 94393860 | ||||||
| chr9:94393911
|
A | ATCCTGTT others(2): Show |
218 | a0001c0001t0002g0004a0001c0001t0002g0029a0001c0001t0002g0036others(215): Show | 221 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(218): Show |
intron_variant | MODIFIER | c.108+18986_108+1898 others(13): Show |
MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr9 | 94393911 | |||||
| chr9:94393995
|
T | A | 1 | a0001c0001t0008g0014 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.108+19068T>A | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 1/11 | chr9 | 94393995 | ||||||
| chr9:94394060
|
T | A | 1 | a0001c0001t0003g0197 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.108+19133T>A | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 1/11 | chr9 | 94394060 | ||||||
| chr9:94394199
|
G | C | 8 | a0001c0002t0009g0209a0001c0002t0009g0210a0001c0002t0009g0211others(5): Show | 8 | HG00140.hp2 HG00741.hp2 HG01255.hp2 others(5): Show |
intron_variant | MODIFIER | c.108+19272G>C | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 1/11 | chr9 | 94394199 | ||||||
| chr9:94394337
|
T | A | 8 | a0001c0002t0009g0209a0001c0002t0009g0210a0001c0002t0009g0211others(5): Show | 8 | HG00140.hp2 HG00741.hp2 HG01255.hp2 others(5): Show |
intron_variant | MODIFIER | c.108+19410T>A | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 1/11 | chr9 | 94394337 | ||||||
| chr9:94394450
|
AT | A | 117 | a0001c0001t0001g0003a0001c0001t0001g0081a0001c0001t0001g0082others(114): Show | 120 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(117): Show |
intron_variant | MODIFIER | c.108+19537delT | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr9 | 94394450 | |||||
| chr9:94394595
|
G | A | 2 | a0001c0001t0001g0225a0001c0001t0001g0241 | 2 | HG03491.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.108+19668G>A | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 1/11 | chr9 | 94394595 | ||||||
| chr9:94394636
|
T | C | 1 | a0001c0001t0005g0033 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.108+19709T>C | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 1/11 | chr9 | 94394636 | ||||||
| chr9:94394787
|
T | A | 1 | a0001c0001t0001g0265 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.108+19860T>A | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 1/11 | chr9 | 94394787 | ||||||
| chr9:94394840
|
T | C | 3 | a0001c0001t0002g0218a0001c0001t0002g0219a0001c0001t0002g0220 | 3 | HG02818.hp1 HG03209.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.108+19913T>C | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 1/11 | chr9 | 94394840 | ||||||
| chr9:94394887
|
C | T | 1 | a0001c0001t0003g0152 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.108+19960C>T | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 1/11 | chr9 | 94394887 | ||||||
| chr9:94394914
|
T | G | 1 | a0001c0001t0002g0315 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.108+19987T>G | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 1/11 | chr9 | 94394914 | ||||||
| chr9:94394915
|
G | GT | 59 | a0001c0001t0002g0218a0001c0001t0002g0219a0001c0001t0002g0220others(56): Show | 59 | HG00140.hp2 HG00544.hp1 HG00639.hp1 others(56): Show |
intron_variant | MODIFIER | c.108+20004dupT | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr9 | 94394915 | |||||
| chr9:94394915
|
G | GTT | 57 | a0001c0001t0002g0029a0001c0001t0002g0036a0001c0001t0002g0039others(54): Show | 58 | HG00597.hp1 HG00639.hp2 HG00642.hp1 others(55): Show |
intron_variant | MODIFIER | c.108+20003_108+2000 others(6): Show |
MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr9 | 94394915 | |||||
| chr9:94394915
|
G | T | 1 | a0001c0001t0002g0315 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.108+19988G>T | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 1/11 | chr9 | 94394915 | ||||||
| chr9:94394918
|
T | TG | 97 | a0001c0001t0002g0004a0001c0001t0002g0118a0001c0001t0002g0119others(94): Show | 99 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(96): Show |
intron_variant | MODIFIER | c.108+19991_108+1999 others(5): Show |
MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 1/11 | chr9 | 94394918 | ||||||
| chr9:94394922
|
T | G | 88 | a0001c0001t0001g0001a0001c0001t0001g0225a0001c0001t0001g0226others(85): Show | 90 | HG00323.hp2 HG00423.hp1 HG00423.hp2 others(87): Show |
intron_variant | MODIFIER | c.108+19995T>G | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 1/11 | chr9 | 94394922 | ||||||
| chr9:94394953
|
G | A | 2 | a0001c0001t0007g0103a0001c0001t0007g0223 | 2 | HG00544.hp1 HG03834.hp2 |
intron_variant | MODIFIER | c.108+20026G>A | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 1/11 | chr9 | 94394953 | ||||||
| chr9:94395005
|
C | T | 2 | a0001c0001t0002g0331a0001c0001t0020g0332 | 2 | HG01255.hp1 HG02895.hp2 |
intron_variant | MODIFIER | c.108+20078C>T | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 1/11 | chr9 | 94395005 | ||||||
| chr9:94395059
|
G | A | 5 | a0001c0001t0001g0230a0001c0001t0001g0266a0001c0001t0001g0267others(2): Show | 5 | HG00438.hp2 HG00673.hp1 NA18970.hp2 others(2): Show |
intron_variant | MODIFIER | c.109-20099G>A | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 1/11 | chr9 | 94395059 | ||||||
| chr9:94395068
|
C | T | 11 | a0001c0001t0006g0107a0001c0001t0006g0108a0001c0001t0006g0109others(8): Show | 11 | HG01243.hp2 HG02109.hp1 HG02280.hp2 others(8): Show |
intron_variant | MODIFIER | c.109-20090C>T | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 1/11 | chr9 | 94395068 | ||||||
| chr9:94395149
|
A | G | 57 | a0001c0001t0002g0029a0001c0001t0002g0036a0001c0001t0002g0039others(54): Show | 58 | HG00597.hp1 HG00639.hp2 HG00642.hp1 others(55): Show |
intron_variant | MODIFIER | c.109-20009A>G | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 1/11 | chr9 | 94395149 | ||||||
| chr9:94395189
|
C | T | 1 | a0001c0001t0017g0022 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.109-19969C>T | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 1/11 | chr9 | 94395189 | ||||||
| chr9:94395232
|
A | G | 10 | a0001c0001t0001g0230a0001c0001t0001g0266a0001c0001t0001g0267others(7): Show | 10 | HG00438.hp2 HG00673.hp1 HG02074.hp2 others(7): Show |
intron_variant | MODIFIER | c.109-19926A>G | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 1/11 | chr9 | 94395232 | ||||||
| chr9:94395270
|
A | G | 2 | a0001c0001t0001g0310a0001c0001t0001g0311 | 2 | HG02258.hp1 HG02622.hp1 |
intron_variant | MODIFIER | c.109-19888A>G | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 1/11 | chr9 | 94395270 | ||||||
| chr9:94395290
|
T | C | 19 | a0001c0001t0002g0318a0001c0001t0002g0319a0001c0001t0002g0321others(16): Show | 19 | HG00639.hp1 HG01109.hp2 HG01256.hp2 others(16): Show |
intron_variant | MODIFIER | c.109-19868T>C | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 1/11 | chr9 | 94395290 | ||||||
| chr9:94395306
|
T | C | 2 | a0001c0001t0002g0331a0001c0001t0020g0332 | 2 | HG01255.hp1 HG02895.hp2 |
intron_variant | MODIFIER | c.109-19852T>C | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 1/11 | chr9 | 94395306 | ||||||
| chr9:94395443
|
GC | G | 57 | a0001c0001t0002g0029a0001c0001t0002g0036a0001c0001t0002g0039others(54): Show | 58 | HG00597.hp1 HG00639.hp2 HG00642.hp1 others(55): Show |
intron_variant | MODIFIER | c.109-19714delC | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 1/11 | chr9 | 94395443 | ||||||
| chr9:94395545
|
G | T | 97 | a0001c0001t0002g0004a0001c0001t0002g0118a0001c0001t0002g0119others(94): Show | 99 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(96): Show |
intron_variant | MODIFIER | c.109-19613G>T | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 1/11 | chr9 | 94395545 | ||||||
| chr9:94395722
|
A | G | 3 | a0001c0001t0002g0218a0001c0001t0002g0219a0001c0001t0002g0220 | 3 | HG02818.hp1 HG03209.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.109-19436A>G | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 1/11 | chr9 | 94395722 | ||||||
| chr9:94395945
|
G | A | 1 | a0001c0001t0001g0268 | 1 | NA18939.hp1 | intron_variant | MODIFIER | c.109-19213G>A | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 1/11 | chr9 | 94395945 | ||||||
| chr9:94396005
|
T | C | 1 | a0001c0001t0003g0152 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.109-19153T>C | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 1/11 | chr9 | 94396005 | ||||||
| chr9:94396141
|
GATA | G | 11 | a0001c0001t0006g0107a0001c0001t0006g0108a0001c0001t0006g0109others(8): Show | 11 | HG01243.hp2 HG02109.hp1 HG02280.hp2 others(8): Show |
intron_variant | MODIFIER | c.109-19012_109-1901 others(7): Show |
MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr9 | 94396141 | |||||
| chr9:94396203
|
G | A | 307 | a0001c0001t0001g0001a0001c0001t0001g0225a0001c0001t0001g0226others(304): Show | 312 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(309): Show |
intron_variant | MODIFIER | c.109-18955G>A | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 1/11 | chr9 | 94396203 | ||||||
| chr9:94396447
|
G | A | 97 | a0001c0001t0002g0004a0001c0001t0002g0118a0001c0001t0002g0119others(94): Show | 99 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(96): Show |
intron_variant | MODIFIER | c.109-18711G>A | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 1/11 | chr9 | 94396447 | ||||||
| chr9:94396492
|
G | A | 1 | a0001c0001t0002g0339 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.109-18666G>A | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 1/11 | chr9 | 94396492 | ||||||
| chr9:94396517
|
C | T | 1 | a0001c0001t0001g0230 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.109-18641C>T | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 1/11 | chr9 | 94396517 | ||||||
| chr9:94396563
|
A | G | 1 | a0001c0001t0008g0344 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.109-18595A>G | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 1/11 | chr9 | 94396563 | ||||||
| chr9:94396596
|
G | A | 320 | a0001c0001t0001g0001a0001c0001t0001g0225a0001c0001t0001g0226others(317): Show | 325 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(322): Show |
intron_variant | MODIFIER | c.109-18562G>A | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 1/11 | chr9 | 94396596 | ||||||
| chr9:94396683
|
C | T | 218 | a0001c0001t0002g0004a0001c0001t0002g0029a0001c0001t0002g0036others(215): Show | 221 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(218): Show |
intron_variant | MODIFIER | c.109-18475C>T | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 1/11 | chr9 | 94396683 | ||||||
| chr9:94396705
|
T | C | 1 | a0001c0001t0001g0269 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.109-18453T>C | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 1/11 | chr9 | 94396705 | ||||||
| chr9:94396758
|
C | T | 1 | a0001c0001t0017g0022 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.109-18400C>T | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 1/11 | chr9 | 94396758 | ||||||
| chr9:94396801
|
G | A | 1 | a0001c0001t0002g0194 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.109-18357G>A | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 1/11 | chr9 | 94396801 | ||||||
| chr9:94396957
|
A | T | 1 | a0001c0002t0009g0211 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.109-18201A>T | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 1/11 | chr9 | 94396957 | ||||||
| chr9:94397001
|
C | T | 97 | a0001c0001t0002g0004a0001c0001t0002g0118a0001c0001t0002g0119others(94): Show | 99 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(96): Show |
intron_variant | MODIFIER | c.109-18157C>T | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 1/11 | chr9 | 94397001 | ||||||
| chr9:94397144
|
C | T | 65 | a0001c0001t0002g0153a0001c0001t0002g0180a0001c0001t0003g0120others(62): Show | 66 | HG00140.hp1 HG00280.hp1 HG00408.hp1 others(63): Show |
intron_variant | MODIFIER | c.109-18014C>T | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 1/11 | chr9 | 94397144 | ||||||
| chr9:94397354
|
T | C | 1 | a0001c0001t0003g0205 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.109-17804T>C | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 1/11 | chr9 | 94397354 | ||||||
| chr9:94397404
|
T | C | 57 | a0001c0001t0002g0029a0001c0001t0002g0036a0001c0001t0002g0039others(54): Show | 58 | HG00597.hp1 HG00639.hp2 HG00642.hp1 others(55): Show |
intron_variant | MODIFIER | c.109-17754T>C | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 1/11 | chr9 | 94397404 | ||||||
| chr9:94397487
|
GA | G | 279 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0081others(276): Show | 284 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(281): Show |
intron_variant | MODIFIER | c.109-17660delA | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr9 | 94397487 | |||||
| chr9:94397501
|
A | G | 3 | a0001c0001t0001g0304a0001c0001t0001g0305a0001c0001t0001g0306 | 3 | HG02451.hp2 HG03471.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.109-17657A>G | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 1/11 | chr9 | 94397501 | ||||||
| chr9:94397666
|
C | T | 8 | a0001c0002t0009g0209a0001c0002t0009g0210a0001c0002t0009g0211others(5): Show | 8 | HG00140.hp2 HG00741.hp2 HG01255.hp2 others(5): Show |
intron_variant | MODIFIER | c.109-17492C>T | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 1/11 | chr9 | 94397666 | ||||||
| chr9:94397693
|
G | A | 4 | a0001c0001t0008g0014a0001c0001t0008g0015a0001c0001t0008g0016others(1): Show | 4 | HG01081.hp1 HG02559.hp1 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.109-17465G>A | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 1/11 | chr9 | 94397693 | ||||||
| chr9:94397700
|
G | C | 218 | a0001c0001t0002g0004a0001c0001t0002g0029a0001c0001t0002g0036others(215): Show | 221 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(218): Show |
intron_variant | MODIFIER | c.109-17458G>C | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 1/11 | chr9 | 94397700 | ||||||
| chr9:94397756
|
G | A | 1 | a0001c0001t0002g0316 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.109-17402G>A | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 1/11 | chr9 | 94397756 | ||||||
| chr9:94397869
|
C | G | 2 | a0001c0001t0003g0204a0001c0001t0004g0067 | 2 | HG02602.hp2 NA18995.hp2 |
intron_variant | MODIFIER | c.109-17289C>G | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 1/11 | chr9 | 94397869 | ||||||
| chr9:94397901
|
G | T | 1 | a0001c0001t0004g0067 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.109-17257G>T | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 1/11 | chr9 | 94397901 | ||||||
| chr9:94398008
|
C | G | 89 | a0001c0001t0001g0001a0001c0001t0001g0225a0001c0001t0001g0226others(86): Show | 91 | HG00323.hp2 HG00408.hp2 HG00423.hp1 others(88): Show |
intron_variant | MODIFIER | c.109-17150C>G | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 1/11 | chr9 | 94398008 | ||||||
| chr9:94398043
|
A | G | 218 | a0001c0001t0002g0004a0001c0001t0002g0029a0001c0001t0002g0036others(215): Show | 221 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(218): Show |
intron_variant | MODIFIER | c.109-17115A>G | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 1/11 | chr9 | 94398043 | ||||||
| chr9:94398070
|
G | C | 3 | a0001c0001t0002g0218a0001c0001t0002g0219a0001c0001t0002g0220 | 3 | HG02818.hp1 HG03209.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.109-17088G>C | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 1/11 | chr9 | 94398070 | ||||||
| chr9:94398170
|
A | G | 60 | a0001c0001t0002g0315a0001c0001t0002g0316a0001c0001t0002g0317others(57): Show | 60 | HG00140.hp2 HG00544.hp1 HG00639.hp1 others(57): Show |
intron_variant | MODIFIER | c.109-16988A>G | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 1/11 | chr9 | 94398170 | ||||||
| chr9:94398224
|
G | GT | 57 | a0001c0001t0002g0029a0001c0001t0002g0036a0001c0001t0002g0039others(54): Show | 58 | HG00597.hp1 HG00639.hp2 HG00642.hp1 others(55): Show |
intron_variant | MODIFIER | c.109-16925dupT | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr9 | 94398224 | |||||
| chr9:94398233
|
T | A | 2 | a0001c0001t0013g0023a0001c0001t0013g0024 | 2 | HG02040.hp2 HG02132.hp2 |
intron_variant | MODIFIER | c.109-16925T>A | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 1/11 | chr9 | 94398233 | ||||||
| chr9:94398354
|
G | T | 7 | a0001c0001t0005g0002a0001c0001t0005g0030a0001c0001t0005g0031others(4): Show | 8 | HG01069.hp1 HG01071.hp1 HG02615.hp2 others(5): Show |
intron_variant | MODIFIER | c.109-16804G>T | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 1/11 | chr9 | 94398354 | ||||||
| chr9:94398561
|
A | G | 1 | a0001c0001t0008g0012 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.109-16597A>G | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 1/11 | chr9 | 94398561 | ||||||
| chr9:94398591
|
C | T | 1 | a0001c0001t0004g0074 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.109-16567C>T | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 1/11 | chr9 | 94398591 | ||||||
| chr9:94398831
|
T | G | 58 | a0001c0001t0002g0029a0001c0001t0002g0036a0001c0001t0002g0039others(55): Show | 59 | HG00597.hp1 HG00639.hp2 HG00642.hp1 others(56): Show |
intron_variant | MODIFIER | c.109-16327T>G | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 1/11 | chr9 | 94398831 | ||||||
| chr9:94398899
|
C | T | 97 | a0001c0001t0002g0004a0001c0001t0002g0118a0001c0001t0002g0119others(94): Show | 99 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(96): Show |
intron_variant | MODIFIER | c.109-16259C>T | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 1/11 | chr9 | 94398899 | ||||||
| chr9:94399042
|
C | T | 4 | a0001c0001t0008g0014a0001c0001t0008g0015a0001c0001t0008g0016others(1): Show | 4 | HG01081.hp1 HG02559.hp1 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.109-16116C>T | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 1/11 | chr9 | 94399042 | ||||||
| chr9:94399047
|
T | A | 8 | a0001c0002t0009g0209a0001c0002t0009g0210a0001c0002t0009g0211others(5): Show | 8 | HG00140.hp2 HG00741.hp2 HG01255.hp2 others(5): Show |
intron_variant | MODIFIER | c.109-16111T>A | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 1/11 | chr9 | 94399047 | ||||||
| chr9:94399058
|
C | T | 3 | a0001c0001t0002g0218a0001c0001t0002g0219a0001c0001t0002g0220 | 3 | HG02818.hp1 HG03209.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.109-16100C>T | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 1/11 | chr9 | 94399058 | ||||||
| chr9:94399116
|
C | T | 97 | a0001c0001t0002g0004a0001c0001t0002g0118a0001c0001t0002g0119others(94): Show | 99 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(96): Show |
intron_variant | MODIFIER | c.109-16042C>T | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 1/11 | chr9 | 94399116 | ||||||
| chr9:94399147
|
C | G | 1 | a0001c0001t0001g0255 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.109-16011C>G | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 1/11 | chr9 | 94399147 | ||||||
| chr9:94399183
|
C | T | 3 | a0001c0001t0007g0099a0001c0001t0007g0100a0001c0001t0007g0105 | 3 | HG02922.hp1 HG03516.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.109-15975C>T | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 1/11 | chr9 | 94399183 | ||||||
| chr9:94399254
|
A | G | 3 | a0001c0001t0002g0218a0001c0001t0002g0219a0001c0001t0002g0220 | 3 | HG02818.hp1 HG03209.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.109-15904A>G | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 1/11 | chr9 | 94399254 | ||||||
| chr9:94399301
|
G | C | 1 | a0001c0001t0017g0022 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.109-15857G>C | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 1/11 | chr9 | 94399301 | ||||||
| chr9:94399363
|
C | T | 160 | a0001c0001t0002g0004a0001c0001t0002g0118a0001c0001t0002g0119others(157): Show | 162 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(159): Show |
intron_variant | MODIFIER | c.109-15795C>T | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 1/11 | chr9 | 94399363 | ||||||
| chr9:94399399
|
T | C | 4 | a0001c0001t0001g0232a0001c0001t0001g0233a0001c0001t0001g0234others(1): Show | 4 | HG01256.hp1 HG01258.hp1 HG02004.hp2 others(1): Show |
intron_variant | MODIFIER | c.109-15759T>C | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 1/11 | chr9 | 94399399 | ||||||
| chr9:94399428
|
G | A | 1 | a0001c0001t0003g0125 | 1 | NA19001.hp1 | intron_variant | MODIFIER | c.109-15730G>A | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 1/11 | chr9 | 94399428 | ||||||
| chr9:94399538
|
A | T | 11 | a0001c0001t0006g0107a0001c0001t0006g0108a0001c0001t0006g0109others(8): Show | 11 | HG01243.hp2 HG02109.hp1 HG02280.hp2 others(8): Show |
intron_variant | MODIFIER | c.109-15620A>T | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 1/11 | chr9 | 94399538 | ||||||
| chr9:94399608
|
A | G | 89 | a0001c0001t0001g0001a0001c0001t0001g0225a0001c0001t0001g0226others(86): Show | 91 | HG00323.hp2 HG00408.hp2 HG00423.hp1 others(88): Show |
intron_variant | MODIFIER | c.109-15550A>G | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 1/11 | chr9 | 94399608 | ||||||
| chr9:94399730
|
C | T | 4 | a0001c0001t0005g0018a0001c0001t0005g0019a0001c0001t0005g0020others(1): Show | 4 | HG01081.hp2 HG01109.hp1 HG02486.hp2 others(1): Show |
intron_variant | MODIFIER | c.109-15428C>T | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 1/11 | chr9 | 94399730 | ||||||
| chr9:94399784
|
G | T | 217 | a0001c0001t0002g0004a0001c0001t0002g0029a0001c0001t0002g0036others(214): Show | 220 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(217): Show |
intron_variant | MODIFIER | c.109-15374G>T | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 1/11 | chr9 | 94399784 | ||||||
| chr9:94399807
|
C | CT | 37 | a0001c0001t0002g0004a0001c0001t0002g0118a0001c0001t0002g0119others(34): Show | 39 | HG00099.hp1 HG00408.hp1 HG00558.hp2 others(36): Show |
intron_variant | MODIFIER | c.109-15336dupT | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr9 | 94399807 | |||||
| chr9:94399807
|
CT | C | 184 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0081others(181): Show | 187 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(184): Show |
intron_variant | MODIFIER | c.109-15336delT | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr9 | 94399807 | |||||
| chr9:94399823
|
G | A | 1 | a0001c0001t0002g0153 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.109-15335G>A | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 1/11 | chr9 | 94399823 | ||||||
| chr9:94399835
|
C | T | 1 | a0001c0001t0004g0066 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.109-15323C>T | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 1/11 | chr9 | 94399835 | ||||||
| chr9:94399868
|
C | T | 32 | a0001c0001t0002g0315a0001c0001t0002g0316a0001c0001t0002g0317others(29): Show | 32 | HG00639.hp1 HG01109.hp2 HG01255.hp1 others(29): Show |
intron_variant | MODIFIER | c.109-15290C>T | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 1/11 | chr9 | 94399868 | ||||||
| chr9:94399906
|
T | G | 160 | a0001c0001t0002g0004a0001c0001t0002g0118a0001c0001t0002g0119others(157): Show | 162 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(159): Show |
intron_variant | MODIFIER | c.109-15252T>G | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 1/11 | chr9 | 94399906 | ||||||
| chr9:94399963
|
G | A | 1 | a0001c0001t0017g0022 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.109-15195G>A | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 1/11 | chr9 | 94399963 | ||||||
| chr9:94399975
|
A | G | 9 | a0001c0001t0007g0099a0001c0001t0007g0100a0001c0001t0007g0101others(6): Show | 9 | HG00544.hp1 HG01884.hp1 HG02630.hp1 others(6): Show |
intron_variant | MODIFIER | c.109-15183A>G | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 1/11 | chr9 | 94399975 | ||||||
| chr9:94400038
|
T | C | 160 | a0001c0001t0002g0004a0001c0001t0002g0118a0001c0001t0002g0119others(157): Show | 162 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(159): Show |
intron_variant | MODIFIER | c.109-15120T>C | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 1/11 | chr9 | 94400038 | ||||||
| chr9:94400055
|
C | T | 8 | a0001c0001t0003g0127a0001c0001t0003g0135a0001c0001t0003g0136others(5): Show | 8 | HG01070.hp1 HG01123.hp1 HG01517.hp2 others(5): Show |
intron_variant | MODIFIER | c.109-15103C>T | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 1/11 | chr9 | 94400055 | ||||||
| chr9:94400060
|
C | G | 160 | a0001c0001t0002g0004a0001c0001t0002g0118a0001c0001t0002g0119others(157): Show | 162 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(159): Show |
intron_variant | MODIFIER | c.109-15098C>G | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 1/11 | chr9 | 94400060 | ||||||
| chr9:94400171
|
C | T | 1 | a0001c0001t0002g0318 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.109-14987C>T | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 1/11 | chr9 | 94400171 | ||||||
| chr9:94400186
|
G | A | 1 | a0001c0001t0003g0154 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.109-14972G>A | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 1/11 | chr9 | 94400186 | ||||||
| chr9:94400208
|
TATGTACC others(10): Show |
T | 3 | a0001c0001t0002g0340a0001c0001t0002g0341a0001c0001t0002g0342 | 3 | HG01884.hp2 HG02886.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.109-14944_109-1492 others(21): Show |
MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr9 | 94400208 | |||||
| chr9:94400228
|
G | T | 2 | a0001c0001t0013g0023a0001c0001t0013g0024 | 2 | HG02040.hp2 HG02132.hp2 |
intron_variant | MODIFIER | c.109-14930G>T | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 1/11 | chr9 | 94400228 | ||||||
| chr9:94400234
|
A | G | 1 | a0001c0001t0003g0126 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.109-14924A>G | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 1/11 | chr9 | 94400234 | ||||||
| chr9:94400496
|
T | G | 46 | a0001c0001t0002g0029a0001c0001t0002g0036a0001c0001t0002g0039others(43): Show | 46 | HG00597.hp1 HG00639.hp2 HG00642.hp1 others(43): Show |
intron_variant | MODIFIER | c.109-14662T>G | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 1/11 | chr9 | 94400496 | ||||||
| chr9:94400509
|
G | GA | 167 | a0001c0001t0001g0098a0001c0001t0002g0004a0001c0001t0002g0029others(164): Show | 170 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(167): Show |
intron_variant | MODIFIER | c.109-14637dupA | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr9 | 94400509 | |||||
| chr9:94400544
|
A | G | 1 | a0001c0001t0002g0148 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.109-14614A>G | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 1/11 | chr9 | 94400544 | ||||||
| chr9:94400567
|
T | C | 2 | a0001c0001t0008g0009a0001c0001t0008g0010 | 2 | HG02818.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.109-14591T>C | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 1/11 | chr9 | 94400567 | ||||||
| chr9:94400568
|
G | GA | 198 | a0001c0001t0002g0004a0001c0001t0002g0029a0001c0001t0002g0036others(195): Show | 201 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(198): Show |
intron_variant | MODIFIER | c.109-14577dupA | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr9 | 94400568 | |||||
| chr9:94400568
|
G | GAAAAA | 11 | a0001c0001t0006g0107a0001c0001t0006g0108a0001c0001t0006g0109others(8): Show | 11 | HG01243.hp2 HG02109.hp1 HG02280.hp2 others(8): Show |
intron_variant | MODIFIER | c.109-14581_109-1457 others(9): Show |
MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr9 | 94400568 | |||||
| chr9:94400702
|
G | A | 2 | a0001c0001t0013g0023a0001c0001t0013g0024 | 2 | HG02040.hp2 HG02132.hp2 |
intron_variant | MODIFIER | c.109-14456G>A | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 1/11 | chr9 | 94400702 | ||||||
| chr9:94400848
|
A | C | 10 | a0001c0001t0008g0009a0001c0001t0008g0010a0001c0001t0008g0011others(7): Show | 10 | HG01081.hp1 HG02280.hp1 HG02559.hp1 others(7): Show |
intron_variant | MODIFIER | c.109-14310A>C | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 1/11 | chr9 | 94400848 | ||||||
| chr9:94400959
|
C | CTT | 9 | a0001c0001t0007g0099a0001c0001t0007g0100a0001c0001t0007g0101others(6): Show | 9 | HG00544.hp1 HG01884.hp1 HG02630.hp1 others(6): Show |
intron_variant | MODIFIER | c.109-14197_109-1419 others(6): Show |
MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr9 | 94400959 | |||||
| chr9:94401088
|
C | CT | 10 | a0001c0001t0008g0009a0001c0001t0008g0010a0001c0001t0008g0011others(7): Show | 10 | HG01081.hp1 HG02280.hp1 HG02559.hp1 others(7): Show |
intron_variant | MODIFIER | c.109-14058dupT | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr9 | 94401088 | |||||
| chr9:94401088
|
CT | C | 7 | a0001c0001t0004g0045a0001c0001t0004g0046a0001c0001t0004g0047others(4): Show | 7 | NA18995.hp2 NA19000.hp2 NA19001.hp2 others(4): Show |
intron_variant | MODIFIER | c.109-14058delT | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr9 | 94401088 | |||||
| chr9:94401151
|
A | G | 1 | a0001c0001t0002g0220 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.109-14007A>G | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 1/11 | chr9 | 94401151 | ||||||
| chr9:94401193
|
C | T | 1 | a0001c0001t0008g0344 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.109-13965C>T | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 1/11 | chr9 | 94401193 | ||||||
| chr9:94401194
|
G | A | 1 | a0001c0001t0001g0257 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.109-13964G>A | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 1/11 | chr9 | 94401194 | ||||||
| chr9:94401202
|
A | G | 57 | a0001c0001t0002g0029a0001c0001t0002g0036a0001c0001t0002g0039others(54): Show | 58 | HG00597.hp1 HG00639.hp2 HG00642.hp1 others(55): Show |
intron_variant | MODIFIER | c.109-13956A>G | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 1/11 | chr9 | 94401202 | ||||||
| chr9:94401305
|
G | T | 10 | a0001c0001t0008g0009a0001c0001t0008g0010a0001c0001t0008g0011others(7): Show | 10 | HG01081.hp1 HG02280.hp1 HG02559.hp1 others(7): Show |
intron_variant | MODIFIER | c.109-13853G>T | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 1/11 | chr9 | 94401305 | ||||||
| chr9:94401506
|
T | A | 5 | a0001c0001t0005g0002a0001c0001t0005g0030a0001c0001t0005g0031others(2): Show | 6 | HG01069.hp1 HG01071.hp1 HG02809.hp2 others(3): Show |
intron_variant | MODIFIER | c.109-13652T>A | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 1/11 | chr9 | 94401506 | ||||||
| chr9:94401601
|
G | C | 4 | a0001c0001t0005g0018a0001c0001t0005g0019a0001c0001t0005g0020others(1): Show | 4 | HG01081.hp2 HG01109.hp1 HG02486.hp2 others(1): Show |
intron_variant | MODIFIER | c.109-13557G>C | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 1/11 | chr9 | 94401601 | ||||||
| chr9:94401639
|
G | C | 3 | a0001c0001t0008g0015a0001c0001t0008g0016a0001c0001t0008g0017 | 3 | HG01081.hp1 HG02559.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.109-13519G>C | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 1/11 | chr9 | 94401639 | ||||||
| chr9:94401650
|
G | C | 1 | a0001c0001t0017g0022 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.109-13508G>C | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 1/11 | chr9 | 94401650 | ||||||
| chr9:94401876
|
G | A | 32 | a0001c0001t0002g0315a0001c0001t0002g0316a0001c0001t0002g0317others(29): Show | 32 | HG00639.hp1 HG01109.hp2 HG01255.hp1 others(29): Show |
intron_variant | MODIFIER | c.109-13282G>A | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 1/11 | chr9 | 94401876 | ||||||
| chr9:94401915
|
A | G | 11 | a0001c0001t0006g0107a0001c0001t0006g0108a0001c0001t0006g0109others(8): Show | 11 | HG01243.hp2 HG02109.hp1 HG02280.hp2 others(8): Show |
intron_variant | MODIFIER | c.109-13243A>G | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 1/11 | chr9 | 94401915 | ||||||
| chr9:94401973
|
C | T | 1 | a0001c0001t0002g0132 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.109-13185C>T | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 1/11 | chr9 | 94401973 | ||||||
| chr9:94401994
|
G | A | 32 | a0001c0001t0002g0315a0001c0001t0002g0316a0001c0001t0002g0317others(29): Show | 32 | HG00639.hp1 HG01109.hp2 HG01255.hp1 others(29): Show |
intron_variant | MODIFIER | c.109-13164G>A | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 1/11 | chr9 | 94401994 | ||||||
| chr9:94402032
|
G | A | 2 | a0001c0001t0013g0023a0001c0001t0013g0024 | 2 | HG02040.hp2 HG02132.hp2 |
intron_variant | MODIFIER | c.109-13126G>A | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 1/11 | chr9 | 94402032 | ||||||
| chr9:94402126
|
C | A | 11 | a0001c0001t0006g0107a0001c0001t0006g0108a0001c0001t0006g0109others(8): Show | 11 | HG01243.hp2 HG02109.hp1 HG02280.hp2 others(8): Show |
intron_variant | MODIFIER | c.109-13032C>A | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 1/11 | chr9 | 94402126 | ||||||
| chr9:94402198
|
G | A | 1 | a0001c0001t0007g0102 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.109-12960G>A | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 1/11 | chr9 | 94402198 | ||||||
| chr9:94402254
|
G | A | 97 | a0001c0001t0002g0004a0001c0001t0002g0118a0001c0001t0002g0119others(94): Show | 99 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(96): Show |
intron_variant | MODIFIER | c.109-12904G>A | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 1/11 | chr9 | 94402254 | ||||||
| chr9:94402300
|
A | G | 7 | a0001c0001t0005g0002a0001c0001t0005g0030a0001c0001t0005g0031others(4): Show | 8 | HG01069.hp1 HG01071.hp1 HG02615.hp2 others(5): Show |
intron_variant | MODIFIER | c.109-12858A>G | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 1/11 | chr9 | 94402300 | ||||||
| chr9:94402401
|
G | GT | 49 | a0001c0001t0002g0315a0001c0001t0002g0316a0001c0001t0002g0317others(46): Show | 49 | HG00140.hp2 HG00544.hp1 HG00639.hp1 others(46): Show |
intron_variant | MODIFIER | c.109-12750dupT | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr9 | 94402401 | |||||
| chr9:94402408
|
T | A | 2 | a0001c0001t0013g0023a0001c0001t0013g0024 | 2 | HG02040.hp2 HG02132.hp2 |
intron_variant | MODIFIER | c.109-12750T>A | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 1/11 | chr9 | 94402408 | ||||||
| chr9:94402826
|
A | G | 57 | a0001c0001t0002g0029a0001c0001t0002g0036a0001c0001t0002g0039others(54): Show | 58 | HG00597.hp1 HG00639.hp2 HG00642.hp1 others(55): Show |
intron_variant | MODIFIER | c.109-12332A>G | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 1/11 | chr9 | 94402826 | ||||||
| chr9:94402966
|
A | G | 160 | a0001c0001t0002g0004a0001c0001t0002g0118a0001c0001t0002g0119others(157): Show | 162 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(159): Show |
intron_variant | MODIFIER | c.109-12192A>G | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 1/11 | chr9 | 94402966 | ||||||
| chr9:94403263
|
A | C | 57 | a0001c0001t0002g0029a0001c0001t0002g0036a0001c0001t0002g0039others(54): Show | 58 | HG00597.hp1 HG00639.hp2 HG00642.hp1 others(55): Show |
intron_variant | MODIFIER | c.109-11895A>C | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 1/11 | chr9 | 94403263 | ||||||
| chr9:94403282
|
G | A | 5 | a0001c0001t0005g0002a0001c0001t0005g0030a0001c0001t0005g0031others(2): Show | 6 | HG01069.hp1 HG01071.hp1 HG02809.hp2 others(3): Show |
intron_variant | MODIFIER | c.109-11876G>A | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 1/11 | chr9 | 94403282 | ||||||
| chr9:94403415
|
G | A | 1 | a0001c0001t0002g0318 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.109-11743G>A | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 1/11 | chr9 | 94403415 | ||||||
| chr9:94403416
|
G | T | 1 | a0001c0001t0017g0022 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.109-11742G>T | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 1/11 | chr9 | 94403416 | ||||||
| chr9:94403503
|
C | CT | 37 | a0001c0001t0002g0315a0001c0001t0002g0316a0001c0001t0002g0317others(34): Show | 37 | HG00140.hp1 HG00639.hp1 HG01074.hp2 others(34): Show |
intron_variant | MODIFIER | c.109-11642dupT | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr9 | 94403503 | |||||
| chr9:94403503
|
CT | C | 8 | a0001c0001t0001g0258a0001c0001t0001g0291a0001c0001t0002g0138others(5): Show | 8 | HG02165.hp1 HG02735.hp1 HG02818.hp2 others(5): Show |
intron_variant | MODIFIER | c.109-11642delT | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr9 | 94403503 | |||||
| chr9:94403535
|
A | G | 2 | a0001c0001t0003g0177a0001c0001t0003g0178 | 2 | HG01074.hp2 NA20752.hp1 |
intron_variant | MODIFIER | c.109-11623A>G | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 1/11 | chr9 | 94403535 | ||||||
| chr9:94403552
|
T | A | 89 | a0001c0001t0001g0001a0001c0001t0001g0225a0001c0001t0001g0226others(86): Show | 91 | HG00323.hp2 HG00408.hp2 HG00423.hp1 others(88): Show |
intron_variant | MODIFIER | c.109-11606T>A | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 1/11 | chr9 | 94403552 | ||||||
| chr9:94403585
|
G | C | 8 | a0001c0002t0009g0209a0001c0002t0009g0210a0001c0002t0009g0211others(5): Show | 8 | HG00140.hp2 HG00741.hp2 HG01255.hp2 others(5): Show |
intron_variant | MODIFIER | c.109-11573G>C | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 1/11 | chr9 | 94403585 | ||||||
| chr9:94404127
|
A | G | 4 | a0001c0001t0003g0176a0001c0001t0003g0177a0001c0001t0003g0178others(1): Show | 4 | HG00140.hp1 HG01074.hp2 HG02602.hp2 others(1): Show |
intron_variant | MODIFIER | c.109-11031A>G | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 1/11 | chr9 | 94404127 | ||||||
| chr9:94404347
|
A | G | 43 | a0001c0001t0001g0238a0001c0001t0001g0287a0001c0001t0002g0029others(40): Show | 43 | HG00597.hp1 HG00639.hp2 HG00642.hp1 others(40): Show |
intron_variant | MODIFIER | c.109-10811A>G | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 1/11 | chr9 | 94404347 | ||||||
| chr9:94404381
|
C | T | 157 | a0001c0001t0002g0004a0001c0001t0002g0118a0001c0001t0002g0119others(154): Show | 158 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(155): Show |
intron_variant | MODIFIER | c.109-10777C>T | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 1/11 | chr9 | 94404381 | ||||||
| chr9:94404405
|
T | C | 23 | a0001c0001t0001g0003a0001c0001t0001g0081a0001c0001t0001g0082others(20): Show | 24 | HG00099.hp2 HG00280.hp2 HG00597.hp2 others(21): Show |
intron_variant | MODIFIER | c.109-10753T>C | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 1/11 | chr9 | 94404405 | ||||||
| chr9:94404525
|
A | G | 1 | a0001c0001t0002g0316 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.109-10633A>G | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 1/11 | chr9 | 94404525 | ||||||
| chr9:94404563
|
T | G | 1 | a0001c0001t0001g0266 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.109-10595T>G | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 1/11 | chr9 | 94404563 | ||||||
| chr9:94404567
|
A | G | 2 | a0001c0001t0007g0103a0001c0001t0007g0223 | 2 | HG00544.hp1 HG03834.hp2 |
intron_variant | MODIFIER | c.109-10591A>G | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 1/11 | chr9 | 94404567 | ||||||
| chr9:94404636
|
G | A | 5 | a0001c0001t0005g0002a0001c0001t0005g0030a0001c0001t0005g0031others(2): Show | 6 | HG01069.hp1 HG01071.hp1 HG02809.hp2 others(3): Show |
intron_variant | MODIFIER | c.109-10522G>A | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 1/11 | chr9 | 94404636 | ||||||
| chr9:94404646
|
T | G | 1 | a0001c0001t0001g0080 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.109-10512T>G | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 1/11 | chr9 | 94404646 | ||||||
| chr9:94404677
|
TTTAA | T | 11 | a0001c0001t0006g0107a0001c0001t0006g0108a0001c0001t0006g0109others(8): Show | 11 | HG01243.hp2 HG02109.hp1 HG02280.hp2 others(8): Show |
intron_variant | MODIFIER | c.109-10478_109-1047 others(8): Show |
MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr9 | 94404677 | |||||
| chr9:94405044
|
A | G | 11 | a0001c0001t0006g0107a0001c0001t0006g0108a0001c0001t0006g0109others(8): Show | 11 | HG01243.hp2 HG02109.hp1 HG02280.hp2 others(8): Show |
intron_variant | MODIFIER | c.109-10114A>G | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 1/11 | chr9 | 94405044 | ||||||
| chr9:94405217
|
C | T | 7 | a0001c0001t0005g0002a0001c0001t0005g0030a0001c0001t0005g0031others(4): Show | 8 | HG01069.hp1 HG01071.hp1 HG02615.hp2 others(5): Show |
intron_variant | MODIFIER | c.109-9941C>T | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 1/11 | chr9 | 94405217 | ||||||
| chr9:94405240
|
A | G | 1 | a0001c0001t0002g0145 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.109-9918A>G | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 1/11 | chr9 | 94405240 | ||||||
| chr9:94405267
|
G | A | 3 | a0001c0001t0004g0049a0001c0001t0004g0071a0001c0001t0004g0072 | 3 | HG00597.hp1 NA19009.hp2 NA19060.hp2 |
intron_variant | MODIFIER | c.109-9891G>A | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 1/11 | chr9 | 94405267 | ||||||
| chr9:94405291
|
C | T | 89 | a0001c0001t0001g0001a0001c0001t0001g0225a0001c0001t0001g0226others(86): Show | 91 | HG00323.hp2 HG00408.hp2 HG00423.hp1 others(88): Show |
intron_variant | MODIFIER | c.109-9867C>T | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 1/11 | chr9 | 94405291 | ||||||
| chr9:94405315
|
G | GA | 7 | a0001c0001t0005g0002a0001c0001t0005g0030a0001c0001t0005g0031others(4): Show | 8 | HG01069.hp1 HG01071.hp1 HG02615.hp2 others(5): Show |
intron_variant | MODIFIER | c.109-9840dupA | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr9 | 94405315 | |||||
| chr9:94405446
|
C | T | 2 | a0001c0001t0001g0248a0001c0001t0001g0249 | 2 | HG03239.hp2 NA18612.hp1 |
intron_variant | MODIFIER | c.109-9712C>T | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 1/11 | chr9 | 94405446 | ||||||
| chr9:94405474
|
G | C | 1 | a0001c0001t0001g0291 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.109-9684G>C | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 1/11 | chr9 | 94405474 | ||||||
| chr9:94405485
|
C | T | 160 | a0001c0001t0002g0004a0001c0001t0002g0118a0001c0001t0002g0119others(157): Show | 162 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(159): Show |
intron_variant | MODIFIER | c.109-9673C>T | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 1/11 | chr9 | 94405485 | ||||||
| chr9:94405493
|
C | T | 3 | a0001c0001t0002g0321a0001c0001t0002g0322a0001c0001t0015g0006 | 3 | HG00639.hp1 HG01109.hp2 HG02683.hp1 |
intron_variant | MODIFIER | c.109-9665C>T | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 1/11 | chr9 | 94405493 | ||||||
| chr9:94405498
|
C | CA | 49 | a0001c0001t0001g0084a0001c0001t0001g0243a0001c0001t0001g0270others(46): Show | 49 | HG00639.hp1 HG00639.hp2 HG01255.hp1 others(46): Show |
intron_variant | MODIFIER | c.109-9640dupA | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr9 | 94405498 | |||||
| chr9:94405498
|
C | CAA | 6 | a0001c0001t0002g0319a0001c0001t0002g0321a0001c0001t0002g0323others(3): Show | 6 | HG01109.hp2 HG02451.hp1 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.109-9641_109-9640d others(4): Show |
MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr9 | 94405498 | |||||
| chr9:94405498
|
CA | C | 6 | a0001c0001t0001g0095a0001c0001t0001g0247a0001c0001t0003g0136others(3): Show | 6 | HG00323.hp2 HG01167.hp1 HG02300.hp2 others(3): Show |
intron_variant | MODIFIER | c.109-9640delA | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr9 | 94405498 | |||||
| chr9:94405596
|
T | G | 1 | a0001c0001t0017g0022 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.109-9562T>G | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 1/11 | chr9 | 94405596 | ||||||
| chr9:94405640
|
T | TTATTCTG others(9): Show |
1 | a0001c0001t0003g0147 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.109-9517_109-9502d others(18): Show |
MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr9 | 94405640 | |||||
| chr9:94405737
|
A | G | 1 | a0001c0001t0017g0022 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.109-9421A>G | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 1/11 | chr9 | 94405737 | ||||||
| chr9:94406014
|
C | G | 60 | a0001c0001t0002g0315a0001c0001t0002g0316a0001c0001t0002g0317others(57): Show | 60 | HG00140.hp2 HG00544.hp1 HG00639.hp1 others(57): Show |
intron_variant | MODIFIER | c.109-9144C>G | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 1/11 | chr9 | 94406014 | ||||||
| chr9:94406066
|
A | AT | 9 | a0001c0001t0001g0077a0001c0001t0001g0078a0001c0001t0001g0079others(6): Show | 9 | HG00323.hp1 HG01358.hp1 HG02040.hp2 others(6): Show |
intron_variant | MODIFIER | c.109-9071dupT | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr9 | 94406066 | |||||
| chr9:94406066
|
A | ATT | 7 | a0001c0001t0001g0081a0001c0001t0001g0085a0001c0001t0008g0010others(4): Show | 7 | HG01975.hp1 HG02280.hp1 HG02818.hp2 others(4): Show |
intron_variant | MODIFIER | c.109-9072_109-9071d others(4): Show |
MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr9 | 94406066 | |||||
| chr9:94406066
|
A | ATTT | 23 | a0001c0001t0001g0003a0001c0001t0001g0082a0001c0001t0001g0084others(20): Show | 24 | HG00099.hp2 HG00642.hp2 HG00733.hp2 others(21): Show |
intron_variant | MODIFIER | c.109-9073_109-9071d others(5): Show |
MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr9 | 94406066 | |||||
| chr9:94406066
|
A | ATTTT | 58 | a0001c0001t0001g0096a0001c0001t0001g0098a0001c0001t0001g0228others(55): Show | 59 | HG00140.hp2 HG00280.hp2 HG00639.hp1 others(56): Show |
intron_variant | MODIFIER | c.109-9074_109-9071d others(6): Show |
MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr9 | 94406066 | |||||
| chr9:94406066
|
A | ATTTTT | 168 | a0001c0001t0001g0001a0001c0001t0001g0225a0001c0001t0001g0226others(165): Show | 172 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(169): Show |
intron_variant | MODIFIER | c.109-9075_109-9071d others(7): Show |
MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr9 | 94406066 | |||||
| chr9:94406066
|
A | ATTTTTT | 57 | a0001c0001t0001g0242a0001c0001t0001g0243a0001c0001t0001g0245others(54): Show | 57 | HG00597.hp1 HG00639.hp2 HG00642.hp1 others(54): Show |
intron_variant | MODIFIER | c.109-9076_109-9071d others(8): Show |
MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr9 | 94406066 | |||||
| chr9:94406066
|
A | ATTTTTTT others(4): Show |
2 | a0001c0001t0002g0218a0001c0001t0002g0220 | 2 | HG02818.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.109-9081_109-9071d others(13): Show |
MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr9 | 94406066 | |||||
| chr9:94406066
|
A | ATTTTTTT others(5): Show |
1 | a0001c0001t0002g0219 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.109-9082_109-9071d others(14): Show |
MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr9 | 94406066 | |||||
| chr9:94406066
|
AT | A | 7 | a0001c0001t0001g0268a0001c0001t0001g0272a0001c0001t0001g0273others(4): Show | 7 | HG02165.hp2 HG02293.hp2 NA18939.hp1 others(4): Show |
intron_variant | MODIFIER | c.109-9071delT | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr9 | 94406066 | |||||
| chr9:94406156
|
C | T | 10 | a0001c0001t0008g0009a0001c0001t0008g0010a0001c0001t0008g0011others(7): Show | 10 | HG01081.hp1 HG02280.hp1 HG02559.hp1 others(7): Show |
intron_variant | MODIFIER | c.109-9002C>T | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 1/11 | chr9 | 94406156 | ||||||
| chr9:94406249
|
A | AT | 3 | a0001c0001t0002g0218a0001c0001t0002g0219a0001c0001t0002g0220 | 3 | HG02818.hp1 HG03209.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.109-8907dupT | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr9 | 94406249 | |||||
| chr9:94406252
|
A | T | 160 | a0001c0001t0002g0004a0001c0001t0002g0118a0001c0001t0002g0119others(157): Show | 162 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(159): Show |
intron_variant | MODIFIER | c.109-8906A>T | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 1/11 | chr9 | 94406252 | ||||||
| chr9:94406365
|
A | G | 1 | a0001c0001t0016g0025 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.109-8793A>G | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 1/11 | chr9 | 94406365 | ||||||
| chr9:94406573
|
A | G | 1 | a0001c0001t0007g0336 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.109-8585A>G | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 1/11 | chr9 | 94406573 | ||||||
| chr9:94406585
|
A | G | 1 | a0001c0001t0004g0061 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.109-8573A>G | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 1/11 | chr9 | 94406585 | ||||||
| chr9:94406637
|
C | G | 1 | a0001c0001t0017g0022 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.109-8521C>G | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 1/11 | chr9 | 94406637 | ||||||
| chr9:94406907
|
G | A | 3 | a0001c0001t0001g0244a0001c0001t0001g0245a0001c0001t0001g0246 | 3 | NA18998.hp2 NA19011.hp2 NA19087.hp2 |
intron_variant | MODIFIER | c.109-8251G>A | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 1/11 | chr9 | 94406907 | ||||||
| chr9:94406910
|
T | C | 1 | a0001c0001t0003g0202 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.109-8248T>C | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 1/11 | chr9 | 94406910 | ||||||
| chr9:94407130
|
GT | G | 53 | a0001c0001t0002g0029a0001c0001t0002g0036a0001c0001t0002g0039others(50): Show | 54 | HG00597.hp1 HG00639.hp2 HG00642.hp1 others(51): Show |
intron_variant | MODIFIER | c.109-8027delT | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 1/11 | chr9 | 94407130 | ||||||
| chr9:94407211
|
T | G | 1 | a0001c0001t0005g0031 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.109-7947T>G | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 1/11 | chr9 | 94407211 | ||||||
| chr9:94407216
|
T | C | 160 | a0001c0001t0002g0004a0001c0001t0002g0118a0001c0001t0002g0119others(157): Show | 162 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(159): Show |
intron_variant | MODIFIER | c.109-7942T>C | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 1/11 | chr9 | 94407216 | ||||||
| chr9:94407381
|
CT | C | 11 | a0001c0001t0001g0291a0001c0001t0001g0309a0001c0001t0002g0334others(8): Show | 11 | HG02165.hp1 HG02451.hp1 NA18948.hp1 others(8): Show |
intron_variant | MODIFIER | c.109-7762delT | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr9 | 94407381 | |||||
| chr9:94407453
|
A | T | 1 | a0001c0001t0002g0132 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.109-7705A>T | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 1/11 | chr9 | 94407453 | ||||||
| chr9:94407479
|
A | G | 1 | a0001c0001t0017g0022 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.109-7679A>G | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 1/11 | chr9 | 94407479 | ||||||
| chr9:94407535
|
C | T | 32 | a0001c0001t0002g0315a0001c0001t0002g0316a0001c0001t0002g0317others(29): Show | 32 | HG00639.hp1 HG01109.hp2 HG01255.hp1 others(29): Show |
intron_variant | MODIFIER | c.109-7623C>T | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 1/11 | chr9 | 94407535 | ||||||
| chr9:94407585
|
G | T | 10 | a0001c0001t0008g0009a0001c0001t0008g0010a0001c0001t0008g0011others(7): Show | 10 | HG01081.hp1 HG02280.hp1 HG02559.hp1 others(7): Show |
intron_variant | MODIFIER | c.109-7573G>T | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 1/11 | chr9 | 94407585 | ||||||
| chr9:94407626
|
C | G | 3 | a0001c0001t0002g0218a0001c0001t0002g0219a0001c0001t0002g0220 | 3 | HG02818.hp1 HG03209.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.109-7532C>G | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 1/11 | chr9 | 94407626 | ||||||
| chr9:94407762
|
G | A | 1 | a0001c0001t0005g0018 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.109-7396G>A | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 1/11 | chr9 | 94407762 | ||||||
| chr9:94407813
|
A | G | 57 | a0001c0001t0002g0029a0001c0001t0002g0036a0001c0001t0002g0039others(54): Show | 58 | HG00597.hp1 HG00639.hp2 HG00642.hp1 others(55): Show |
intron_variant | MODIFIER | c.109-7345A>G | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 1/11 | chr9 | 94407813 | ||||||
| chr9:94407836
|
T | C | 57 | a0001c0001t0002g0029a0001c0001t0002g0036a0001c0001t0002g0039others(54): Show | 58 | HG00597.hp1 HG00639.hp2 HG00642.hp1 others(55): Show |
intron_variant | MODIFIER | c.109-7322T>C | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 1/11 | chr9 | 94407836 | ||||||
| chr9:94408100
|
A | G | 160 | a0001c0001t0002g0004a0001c0001t0002g0118a0001c0001t0002g0119others(157): Show | 162 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(159): Show |
intron_variant | MODIFIER | c.109-7058A>G | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 1/11 | chr9 | 94408100 | ||||||
| chr9:94408140
|
A | C | 1 | a0001c0001t0017g0022 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.109-7018A>C | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 1/11 | chr9 | 94408140 | ||||||
| chr9:94408174
|
T | A | 2 | a0001c0001t0001g0276a0001c0001t0001g0287 | 2 | HG02735.hp2 HG04199.hp2 |
intron_variant | MODIFIER | c.109-6984T>A | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 1/11 | chr9 | 94408174 | ||||||
| chr9:94408222
|
C | A | 57 | a0001c0001t0002g0029a0001c0001t0002g0036a0001c0001t0002g0039others(54): Show | 58 | HG00597.hp1 HG00639.hp2 HG00642.hp1 others(55): Show |
intron_variant | MODIFIER | c.109-6936C>A | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 1/11 | chr9 | 94408222 | ||||||
| chr9:94408311
|
C | G | 3 | a0001c0001t0001g0244a0001c0001t0001g0245a0001c0001t0001g0246 | 3 | NA18998.hp2 NA19011.hp2 NA19087.hp2 |
intron_variant | MODIFIER | c.109-6847C>G | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 1/11 | chr9 | 94408311 | ||||||
| chr9:94408504
|
G | A | 4 | a0001c0001t0001g0077a0001c0001t0001g0078a0001c0001t0001g0079others(1): Show | 4 | HG00323.hp1 HG01358.hp1 HG02559.hp2 others(1): Show |
intron_variant | MODIFIER | c.109-6654G>A | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 1/11 | chr9 | 94408504 | ||||||
| chr9:94408582
|
G | A | 3 | a0001c0001t0002g0218a0001c0001t0002g0219a0001c0001t0002g0220 | 3 | HG02818.hp1 HG03209.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.109-6576G>A | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 1/11 | chr9 | 94408582 | ||||||
| chr9:94408665
|
A | G | 1 | a0001c0001t0001g0238 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.109-6493A>G | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 1/11 | chr9 | 94408665 | ||||||
| chr9:94408825
|
TTG | T | 28 | a0001c0001t0006g0107a0001c0001t0006g0108a0001c0001t0006g0109others(25): Show | 28 | HG00140.hp2 HG00544.hp1 HG00741.hp2 others(25): Show |
intron_variant | MODIFIER | c.109-6331_109-6330d others(4): Show |
MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr9 | 94408825 | |||||
| chr9:94408826
|
TG | T | 106 | a0001c0001t0001g0003a0001c0001t0001g0077a0001c0001t0001g0078others(103): Show | 108 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(105): Show |
intron_variant | MODIFIER | c.109-6331delG | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 1/11 | chr9 | 94408826 | ||||||
| chr9:94408827
|
G | T | 191 | a0001c0001t0001g0001a0001c0001t0001g0094a0001c0001t0001g0225others(188): Show | 195 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(192): Show |
intron_variant | MODIFIER | c.109-6331G>T | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 1/11 | chr9 | 94408827 | ||||||
| chr9:94408829
|
T | G | 10 | a0001c0001t0008g0009a0001c0001t0008g0010a0001c0001t0008g0011others(7): Show | 10 | HG01081.hp1 HG02280.hp1 HG02559.hp1 others(7): Show |
intron_variant | MODIFIER | c.109-6329T>G | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 1/11 | chr9 | 94408829 | ||||||
| chr9:94408831
|
G | GTTT | 6 | a0001c0001t0001g0228a0001c0001t0001g0258a0001c0001t0001g0262others(3): Show | 6 | HG00621.hp1 HG01261.hp1 HG02148.hp1 others(3): Show |
intron_variant | MODIFIER | c.109-6326_109-6324d others(5): Show |
MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr9 | 94408831 | |||||
| chr9:94408831
|
G | T | 92 | a0001c0001t0001g0003a0001c0001t0001g0077a0001c0001t0001g0078others(89): Show | 93 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(90): Show |
intron_variant | MODIFIER | c.109-6327G>T | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 1/11 | chr9 | 94408831 | ||||||
| chr9:94408834
|
T | G | 10 | a0001c0001t0008g0009a0001c0001t0008g0010a0001c0001t0008g0011others(7): Show | 10 | HG01081.hp1 HG02280.hp1 HG02559.hp1 others(7): Show |
intron_variant | MODIFIER | c.109-6324T>G | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 1/11 | chr9 | 94408834 | ||||||
| chr9:94408835
|
G | T | 10 | a0001c0001t0008g0009a0001c0001t0008g0010a0001c0001t0008g0011others(7): Show | 10 | HG01081.hp1 HG02280.hp1 HG02559.hp1 others(7): Show |
intron_variant | MODIFIER | c.109-6323G>T | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 1/11 | chr9 | 94408835 | ||||||
| chr9:94408875
|
T | C | 4 | a0001c0001t0008g0014a0001c0001t0008g0015a0001c0001t0008g0016others(1): Show | 4 | HG01081.hp1 HG02559.hp1 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.109-6283T>C | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 1/11 | chr9 | 94408875 | ||||||
| chr9:94408975
|
C | T | 8 | a0001c0002t0009g0209a0001c0002t0009g0210a0001c0002t0009g0211others(5): Show | 8 | HG00140.hp2 HG00741.hp2 HG01255.hp2 others(5): Show |
intron_variant | MODIFIER | c.109-6183C>T | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 1/11 | chr9 | 94408975 | ||||||
| chr9:94408992
|
A | G | 1 | a0001c0001t0008g0014 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.109-6166A>G | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 1/11 | chr9 | 94408992 | ||||||
| chr9:94409055
|
G | A | 57 | a0001c0001t0002g0029a0001c0001t0002g0036a0001c0001t0002g0039others(54): Show | 58 | HG00597.hp1 HG00639.hp2 HG00642.hp1 others(55): Show |
intron_variant | MODIFIER | c.109-6103G>A | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 1/11 | chr9 | 94409055 | ||||||
| chr9:94409129
|
C | CT | 60 | a0001c0001t0002g0004a0001c0001t0002g0118a0001c0001t0002g0119others(57): Show | 62 | HG00099.hp1 HG00408.hp1 HG00544.hp2 others(59): Show |
intron_variant | MODIFIER | c.109-6002dupT | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr9 | 94409129 | |||||
| chr9:94409129
|
C | CTT | 13 | a0001c0001t0001g0229a0001c0001t0001g0232a0001c0001t0001g0268others(10): Show | 13 | HG01256.hp1 HG02055.hp2 HG02280.hp2 others(10): Show |
intron_variant | MODIFIER | c.109-6003_109-6002d others(4): Show |
MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr9 | 94409129 | |||||
| chr9:94409129
|
C | CTTT | 59 | a0001c0001t0001g0001a0001c0001t0001g0225a0001c0001t0001g0226others(56): Show | 61 | HG00408.hp2 HG00438.hp1 HG00438.hp2 others(58): Show |
intron_variant | MODIFIER | c.109-6004_109-6002d others(5): Show |
MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr9 | 94409129 | |||||
| chr9:94409129
|
C | CTTTT | 20 | a0001c0001t0001g0237a0001c0001t0001g0240a0001c0001t0001g0246others(17): Show | 20 | HG00323.hp2 HG00423.hp1 HG00423.hp2 others(17): Show |
intron_variant | MODIFIER | c.109-6005_109-6002d others(6): Show |
MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr9 | 94409129 | |||||
| chr9:94409129
|
C | CTTTTTT | 7 | a0001c0001t0001g0084a0001c0001t0001g0088a0001c0001t0001g0089others(4): Show | 7 | HG01167.hp1 HG01169.hp1 HG01261.hp2 others(4): Show |
intron_variant | MODIFIER | c.109-6007_109-6002d others(8): Show |
MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr9 | 94409129 | |||||
| chr9:94409129
|
C | CTTTTTTT | 9 | a0001c0001t0001g0082a0001c0001t0001g0085a0001c0001t0001g0090others(6): Show | 9 | HG00099.hp2 HG00280.hp2 HG00733.hp2 others(6): Show |
intron_variant | MODIFIER | c.109-6008_109-6002d others(9): Show |
MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr9 | 94409129 | |||||
| chr9:94409129
|
C | CTTTTTTT others(3): Show |
2 | a0001c0001t0008g0011a0001c0001t0008g0015 | 2 | HG01081.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.109-6011_109-6002d others(12): Show |
MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr9 | 94409129 | |||||
| chr9:94409129
|
C | CTTTTTTT others(4): Show |
5 | a0001c0001t0008g0009a0001c0001t0008g0010a0001c0001t0008g0013others(2): Show | 5 | HG02280.hp1 HG02818.hp2 HG02886.hp1 others(2): Show |
intron_variant | MODIFIER | c.109-6012_109-6002d others(13): Show |
MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr9 | 94409129 | |||||
| chr9:94409129
|
C | CTTTTTTT others(6): Show |
1 | a0001c0001t0008g0017 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.109-6014_109-6002d others(15): Show |
MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr9 | 94409129 | |||||
| chr9:94409129
|
C | CTTTTTTT others(9): Show |
1 | a0001c0001t0008g0344 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.109-6017_109-6002d others(18): Show |
MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr9 | 94409129 | |||||
| chr9:94409129
|
CT | C | 72 | a0001c0001t0002g0029a0001c0001t0002g0039a0001c0001t0002g0040others(69): Show | 72 | HG00544.hp1 HG00597.hp1 HG00642.hp1 others(69): Show |
intron_variant | MODIFIER | c.109-6002delT | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr9 | 94409129 | |||||
| chr9:94409129
|
CTTTTTTT others(4): Show |
C | 1 | a0001c0001t0017g0022 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.109-6012_109-6002d others(13): Show |
MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr9 | 94409129 | |||||
| chr9:94409129
|
CTTTTTTT others(6): Show |
C | 7 | a0001c0001t0004g0045a0001c0001t0004g0046a0001c0001t0004g0047others(4): Show | 7 | NA18995.hp2 NA19000.hp2 NA19001.hp2 others(4): Show |
intron_variant | MODIFIER | c.109-6014_109-6002d others(15): Show |
MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr9 | 94409129 | |||||
| chr9:94409266
|
A | G | 2 | a0001c0001t0001g0085a0001c0001t0001g0093 | 2 | HG02300.hp1 HG03704.hp1 |
intron_variant | MODIFIER | c.109-5892A>G | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 1/11 | chr9 | 94409266 | ||||||
| chr9:94409366
|
GTCTTAAC others(1): Show |
G | 248 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0077others(245): Show | 252 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(249): Show |
intron_variant | MODIFIER | c.109-5783_109-5776d others(10): Show |
MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr9 | 94409366 | |||||
| chr9:94409599
|
A | G | 1 | a0001c0001t0005g0032 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.109-5559A>G | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 1/11 | chr9 | 94409599 | ||||||
| chr9:94409681
|
T | G | 1 | a0001c0001t0016g0025 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.109-5477T>G | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 1/11 | chr9 | 94409681 | ||||||
| chr9:94409703
|
G | T | 1 | a0001c0001t0004g0035 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.109-5455G>T | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 1/11 | chr9 | 94409703 | ||||||
| chr9:94409898
|
G | GTT | 125 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0077others(122): Show | 128 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(125): Show |
intron_variant | MODIFIER | c.109-5259_109-5258d others(4): Show |
MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr9 | 94409898 | |||||
| chr9:94409943
|
T | A | 183 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0077others(180): Show | 187 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(184): Show |
intron_variant | MODIFIER | c.109-5215T>A | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 1/11 | chr9 | 94409943 | ||||||
| chr9:94410247
|
C | T | 1 | a0001c0001t0003g0204 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.109-4911C>T | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 1/11 | chr9 | 94410247 | ||||||
| chr9:94410350
|
A | G | 11 | a0001c0001t0006g0107a0001c0001t0006g0108a0001c0001t0006g0109others(8): Show | 11 | HG01243.hp2 HG02109.hp1 HG02280.hp2 others(8): Show |
intron_variant | MODIFIER | c.109-4808A>G | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 1/11 | chr9 | 94410350 | ||||||
| chr9:94410404
|
AT | A | 181 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0077others(178): Show | 185 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(182): Show |
intron_variant | MODIFIER | c.109-4747delT | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr9 | 94410404 | |||||
| chr9:94410417
|
C | T | 57 | a0001c0001t0002g0029a0001c0001t0002g0036a0001c0001t0002g0039others(54): Show | 58 | HG00597.hp1 HG00639.hp2 HG00642.hp1 others(55): Show |
intron_variant | MODIFIER | c.109-4741C>T | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 1/11 | chr9 | 94410417 | ||||||
| chr9:94410458
|
T | TG | 3 | a0001c0001t0002g0218a0001c0001t0002g0219a0001c0001t0002g0220 | 3 | HG02818.hp1 HG03209.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.109-4699dupG | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr9 | 94410458 | |||||
| chr9:94410506
|
G | A | 2 | a0001c0001t0004g0028a0001c0001t0004g0065 | 2 | HG00639.hp2 HG03688.hp1 |
intron_variant | MODIFIER | c.109-4652G>A | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 1/11 | chr9 | 94410506 | ||||||
| chr9:94410519
|
C | T | 1 | a0001c0001t0003g0129 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.109-4639C>T | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 1/11 | chr9 | 94410519 | ||||||
| chr9:94410664
|
C | T | 183 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0077others(180): Show | 187 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(184): Show |
intron_variant | MODIFIER | c.109-4494C>T | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 1/11 | chr9 | 94410664 | ||||||
| chr9:94410750
|
C | G | 4 | a0001c0001t0001g0077a0001c0001t0001g0078a0001c0001t0001g0079others(1): Show | 4 | HG00323.hp1 HG01358.hp1 HG02559.hp2 others(1): Show |
intron_variant | MODIFIER | c.109-4408C>G | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 1/11 | chr9 | 94410750 | ||||||
| chr9:94410922
|
C | T | 9 | a0001c0001t0007g0099a0001c0001t0007g0100a0001c0001t0007g0101others(6): Show | 9 | HG00544.hp1 HG01884.hp1 HG02630.hp1 others(6): Show |
intron_variant | MODIFIER | c.109-4236C>T | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 1/11 | chr9 | 94410922 | ||||||
| chr9:94411067
|
T | C | 2 | a0001c0001t0013g0023a0001c0001t0013g0024 | 2 | HG02040.hp2 HG02132.hp2 |
intron_variant | MODIFIER | c.109-4091T>C | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 1/11 | chr9 | 94411067 | ||||||
| chr9:94411170
|
T | C | 11 | a0001c0001t0006g0107a0001c0001t0006g0108a0001c0001t0006g0109others(8): Show | 11 | HG01243.hp2 HG02109.hp1 HG02280.hp2 others(8): Show |
intron_variant | MODIFIER | c.109-3988T>C | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 1/11 | chr9 | 94411170 | ||||||
| chr9:94411585
|
G | A | 2 | a0001c0001t0008g0009a0001c0001t0008g0010 | 2 | HG02818.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.109-3573G>A | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 1/11 | chr9 | 94411585 | ||||||
| chr9:94411593
|
A | AT | 28 | a0001c0001t0001g0003a0001c0001t0001g0081a0001c0001t0001g0082others(25): Show | 29 | HG00099.hp2 HG00280.hp2 HG00642.hp2 others(26): Show |
intron_variant | MODIFIER | c.109-3551dupT | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr9 | 94411593 | |||||
| chr9:94411593
|
AT | A | 15 | a0001c0001t0001g0272a0001c0001t0002g0322a0001c0001t0003g0156others(12): Show | 15 | HG00639.hp1 HG01243.hp2 HG02109.hp1 others(12): Show |
intron_variant | MODIFIER | c.109-3551delT | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr9 | 94411593 | |||||
| chr9:94411651
|
C | G | 1 | a0001c0001t0003g0147 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.109-3507C>G | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 1/11 | chr9 | 94411651 | ||||||
| chr9:94411652
|
G | C | 1 | a0001c0001t0003g0147 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.109-3506G>C | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 1/11 | chr9 | 94411652 | ||||||
| chr9:94411719
|
T | A | 1 | a0001c0001t0002g0339 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.109-3439T>A | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 1/11 | chr9 | 94411719 | ||||||
| chr9:94411877
|
C | G | 57 | a0001c0001t0002g0029a0001c0001t0002g0036a0001c0001t0002g0039others(54): Show | 58 | HG00597.hp1 HG00639.hp2 HG00642.hp1 others(55): Show |
intron_variant | MODIFIER | c.109-3281C>G | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 1/11 | chr9 | 94411877 | ||||||
| chr9:94411933
|
A | G | 1 | a0001c0001t0007g0103 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.109-3225A>G | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 1/11 | chr9 | 94411933 | ||||||
| chr9:94412318
|
G | T | 1 | a0001c0001t0017g0022 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.109-2840G>T | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 1/11 | chr9 | 94412318 | ||||||
| chr9:94412568
|
C | A | 2 | a0001c0001t0001g0302a0002c0004t0001g0299 | 2 | HG02293.hp2 NA18975.hp2 |
intron_variant | MODIFIER | c.109-2590C>A | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 1/11 | chr9 | 94412568 | ||||||
| chr9:94412619
|
G | A | 2 | a0001c0001t0004g0027a0001c0001t0004g0050 | 2 | NA19079.hp1 NA19086.hp2 |
intron_variant | MODIFIER | c.109-2539G>A | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 1/11 | chr9 | 94412619 | ||||||
| chr9:94412791
|
A | G | 1 | a0001c0001t0017g0022 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.109-2367A>G | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 1/11 | chr9 | 94412791 | ||||||
| chr9:94412890
|
T | A | 1 | a0001c0001t0007g0104 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.109-2268T>A | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 1/11 | chr9 | 94412890 | ||||||
| chr9:94413006
|
T | A | 1 | a0001c0001t0001g0297 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.109-2152T>A | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 1/11 | chr9 | 94413006 | ||||||
| chr9:94413007
|
A | T | 25 | a0001c0001t0001g0242a0001c0001t0001g0243a0001c0001t0001g0244others(22): Show | 25 | HG00408.hp2 HG00423.hp1 HG00438.hp1 others(22): Show |
intron_variant | MODIFIER | c.109-2151A>T | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 1/11 | chr9 | 94413007 | ||||||
| chr9:94413008
|
A | T | 1 | a0001c0001t0001g0245 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.109-2150A>T | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 1/11 | chr9 | 94413008 | ||||||
| chr9:94413013
|
T | A | 30 | a0001c0001t0001g0242a0001c0001t0001g0243a0001c0001t0001g0244others(27): Show | 30 | HG00408.hp2 HG00423.hp1 HG00438.hp1 others(27): Show |
intron_variant | MODIFIER | c.109-2145T>A | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 1/11 | chr9 | 94413013 | ||||||
| chr9:94413101
|
A | G | 1 | a0001c0001t0002g0319 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.109-2057A>G | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 1/11 | chr9 | 94413101 | ||||||
| chr9:94413192
|
A | T | 1 | a0001c0001t0017g0022 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.109-1966A>T | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 1/11 | chr9 | 94413192 | ||||||
| chr9:94413492
|
G | T | 125 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0077others(122): Show | 128 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(125): Show |
intron_variant | MODIFIER | c.109-1666G>T | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 1/11 | chr9 | 94413492 | ||||||
| chr9:94413605
|
A | ATCCCAG | 10 | a0001c0001t0008g0009a0001c0001t0008g0010a0001c0001t0008g0011others(7): Show | 10 | HG01081.hp1 HG02280.hp1 HG02559.hp1 others(7): Show |
intron_variant | MODIFIER | c.109-1553_109-1552i others(8): Show |
MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 1/11 | chr9 | 94413605 | ||||||
| chr9:94413659
|
C | CA | 101 | a0001c0001t0002g0004a0001c0001t0002g0118a0001c0001t0002g0119others(98): Show | 103 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(100): Show |
intron_variant | MODIFIER | c.109-1481dupA | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr9 | 94413659 | |||||
| chr9:94413659
|
C | CAA | 18 | a0001c0001t0002g0194a0001c0001t0002g0198a0001c0001t0004g0059others(15): Show | 18 | HG00140.hp2 HG00741.hp2 HG01081.hp2 others(15): Show |
intron_variant | MODIFIER | c.109-1482_109-1481d others(4): Show |
MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr9 | 94413659 | |||||
| chr9:94413659
|
C | CAAA | 50 | a0001c0001t0001g0263a0001c0001t0001g0268a0001c0001t0002g0029others(47): Show | 50 | HG00597.hp1 HG00639.hp2 HG00642.hp1 others(47): Show |
intron_variant | MODIFIER | c.109-1483_109-1481d others(5): Show |
MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr9 | 94413659 | |||||
| chr9:94413659
|
C | CAAAA | 102 | a0001c0001t0001g0001a0001c0001t0001g0077a0001c0001t0001g0078others(99): Show | 105 | HG00280.hp2 HG00323.hp1 HG00408.hp2 others(102): Show |
intron_variant | MODIFIER | c.109-1484_109-1481d others(6): Show |
MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr9 | 94413659 | |||||
| chr9:94413659
|
C | CAAAAA | 24 | a0001c0001t0001g0003a0001c0001t0001g0081a0001c0001t0001g0082others(21): Show | 25 | HG00099.hp2 HG00323.hp2 HG00642.hp2 others(22): Show |
intron_variant | MODIFIER | c.109-1485_109-1481d others(7): Show |
MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr9 | 94413659 | |||||
| chr9:94413719
|
A | G | 1 | a0001c0001t0007g0223 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.109-1439A>G | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 1/11 | chr9 | 94413719 | ||||||
| chr9:94413810
|
T | A | 2 | a0001c0001t0001g0310a0001c0001t0001g0311 | 2 | HG02258.hp1 HG02622.hp1 |
intron_variant | MODIFIER | c.109-1348T>A | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 1/11 | chr9 | 94413810 | ||||||
| chr9:94413818
|
C | T | 57 | a0001c0001t0002g0029a0001c0001t0002g0036a0001c0001t0002g0039others(54): Show | 58 | HG00597.hp1 HG00639.hp2 HG00642.hp1 others(55): Show |
intron_variant | MODIFIER | c.109-1340C>T | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 1/11 | chr9 | 94413818 | ||||||
| chr9:94413865
|
A | G | 3 | a0001c0001t0002g0218a0001c0001t0002g0219a0001c0001t0002g0220 | 3 | HG02818.hp1 HG03209.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.109-1293A>G | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 1/11 | chr9 | 94413865 | ||||||
| chr9:94413943
|
G | T | 1 | a0001c0001t0002g0141 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.109-1215G>T | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 1/11 | chr9 | 94413943 | ||||||
| chr9:94414086
|
T | C | 2 | a0001c0001t0012g0005a0001c0001t0012g0167 | 3 | NA18970.hp1 NA19004.hp2 NA19058.hp1 |
intron_variant | MODIFIER | c.109-1072T>C | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 1/11 | chr9 | 94414086 | ||||||
| chr9:94414443
|
G | A | 1 | a0001c0001t0004g0035 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.109-715G>A | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 1/11 | chr9 | 94414443 | ||||||
| chr9:94414446
|
C | T | 126 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0077others(123): Show | 129 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(126): Show |
intron_variant | MODIFIER | c.109-712C>T | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 1/11 | chr9 | 94414446 | ||||||
| chr9:94414683
|
A | G | 2 | a0001c0001t0002g0321a0001c0001t0002g0322 | 2 | HG00639.hp1 HG01109.hp2 |
intron_variant | MODIFIER | c.109-475A>G | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 1/11 | chr9 | 94414683 | ||||||
| chr9:94414686
|
G | A | 2 | a0001c0001t0002g0321a0001c0001t0002g0322 | 2 | HG00639.hp1 HG01109.hp2 |
intron_variant | MODIFIER | c.109-472G>A | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 1/11 | chr9 | 94414686 | ||||||
| chr9:94414728
|
C | T | 1 | a0001c0001t0002g0316 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.109-430C>T | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 1/11 | chr9 | 94414728 | ||||||
| chr9:94414786
|
A | G | 19 | a0001c0001t0002g0318a0001c0001t0002g0319a0001c0001t0002g0321others(16): Show | 19 | HG00639.hp1 HG01109.hp2 HG01256.hp2 others(16): Show |
intron_variant | MODIFIER | c.109-372A>G | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 1/11 | chr9 | 94414786 | ||||||
| chr9:94414831
|
A | G | 43 | a0001c0001t0002g0029a0001c0001t0002g0036a0001c0001t0002g0039others(40): Show | 43 | HG00597.hp1 HG00639.hp2 HG00642.hp1 others(40): Show |
intron_variant | MODIFIER | c.109-327A>G | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 1/11 | chr9 | 94414831 | ||||||
| chr9:94414948
|
A | G | 1 | a0001c0001t0001g0271 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.109-210A>G | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 1/11 | chr9 | 94414948 | ||||||
| chr9:94414950
|
A | G | 245 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0077others(242): Show | 249 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(246): Show |
intron_variant | MODIFIER | c.109-208A>G | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 1/11 | chr9 | 94414950 | ||||||
| chr9:94414952
|
C | T | 1 | a0001c0001t0003g0173 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.109-206C>T | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 1/11 | chr9 | 94414952 | ||||||
| chr9:94414956
|
C | G | 1 | a0001c0001t0001g0271 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.109-202C>G | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 1/11 | chr9 | 94414956 | ||||||
| chr9:94414966
|
G | A | 1 | a0001c0001t0001g0271 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.109-192G>A | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 1/11 | chr9 | 94414966 | ||||||
| chr9:94414978
|
C | T | 1 | a0001c0001t0001g0271 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.109-180C>T | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 1/11 | chr9 | 94414978 | ||||||
| chr9:94415020
|
G | A | 1 | a0001c0001t0002g0329 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.109-138G>A | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 1/11 | chr9 | 94415020 | ||||||
| chr9:94415321
|
G | A | 4 | a0001c0001t0001g0077a0001c0001t0001g0078a0001c0001t0001g0079others(1): Show | 4 | HG00323.hp1 HG01358.hp1 HG02559.hp2 others(1): Show |
intron_variant | MODIFIER | c.204+68G>A | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 2/11 | chr9 | 94415321 | ||||||
| chr9:94415359
|
A | G | 57 | a0001c0001t0002g0029a0001c0001t0002g0036a0001c0001t0002g0039others(54): Show | 58 | HG00597.hp1 HG00639.hp2 HG00642.hp1 others(55): Show |
intron_variant | MODIFIER | c.204+106A>G | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 2/11 | chr9 | 94415359 | ||||||
| chr9:94415385
|
G | GT | 180 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0077others(177): Show | 184 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(181): Show |
intron_variant | MODIFIER | c.204+144dupT | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr9 | 94415385 | |||||
| chr9:94415387
|
T | G | 1 | a0001c0001t0002g0198 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.204+134T>G | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 2/11 | chr9 | 94415387 | ||||||
| chr9:94415471
|
T | G | 183 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0077others(180): Show | 187 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(184): Show |
intron_variant | MODIFIER | c.204+218T>G | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 2/11 | chr9 | 94415471 | ||||||
| chr9:94415544
|
C | T | 125 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0077others(122): Show | 128 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(125): Show |
intron_variant | MODIFIER | c.204+291C>T | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 2/11 | chr9 | 94415544 | ||||||
| chr9:94415571
|
A | G | 6 | a0001c0001t0002g0317a0001c0001t0002g0330a0001c0001t0002g0331others(3): Show | 6 | HG01255.hp1 HG02615.hp1 HG02630.hp2 others(3): Show |
intron_variant | MODIFIER | c.204+318A>G | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 2/11 | chr9 | 94415571 | ||||||
| chr9:94415707
|
A | C | 192 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0077others(189): Show | 196 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(193): Show |
intron_variant | MODIFIER | c.204+454A>C | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 2/11 | chr9 | 94415707 | ||||||
| chr9:94416009
|
C | T | 2 | a0001c0001t0005g0002a0001c0001t0017g0022 | 3 | HG01069.hp1 HG01071.hp1 HG02647.hp2 |
intron_variant | MODIFIER | c.204+756C>T | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 2/11 | chr9 | 94416009 | ||||||
| chr9:94416020
|
T | C | 2 | a0001c0001t0013g0023a0001c0001t0013g0024 | 2 | HG02040.hp2 HG02132.hp2 |
intron_variant | MODIFIER | c.204+767T>C | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 2/11 | chr9 | 94416020 | ||||||
| chr9:94416061
|
G | C | 1 | a0001c0001t0002g0320 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.204+808G>C | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 2/11 | chr9 | 94416061 | ||||||
| chr9:94416081
|
T | C | 32 | a0001c0001t0002g0315a0001c0001t0002g0316a0001c0001t0002g0317others(29): Show | 32 | HG00639.hp1 HG01109.hp2 HG01255.hp1 others(29): Show |
intron_variant | MODIFIER | c.204+828T>C | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 2/11 | chr9 | 94416081 | ||||||
| chr9:94416086
|
C | T | 11 | a0001c0001t0003g0182a0001c0001t0008g0009a0001c0001t0008g0010others(8): Show | 11 | HG01081.hp1 HG02280.hp1 HG02559.hp1 others(8): Show |
intron_variant | MODIFIER | c.204+833C>T | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 2/11 | chr9 | 94416086 | ||||||
| chr9:94416242
|
C | T | 1 | a0001c0001t0017g0022 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.204+989C>T | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 2/11 | chr9 | 94416242 | ||||||
| chr9:94416432
|
C | T | 19 | a0001c0001t0006g0107a0001c0001t0006g0108a0001c0001t0006g0109others(16): Show | 19 | HG00140.hp2 HG00741.hp2 HG01243.hp2 others(16): Show |
intron_variant | MODIFIER | c.204+1179C>T | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 2/11 | chr9 | 94416432 | ||||||
| chr9:94416466
|
G | A | 1 | a0001c0001t0001g0253 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.204+1213G>A | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 2/11 | chr9 | 94416466 | ||||||
| chr9:94416507
|
C | T | 2 | a0001c0001t0013g0023a0001c0001t0013g0024 | 2 | HG02040.hp2 HG02132.hp2 |
intron_variant | MODIFIER | c.204+1254C>T | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 2/11 | chr9 | 94416507 | ||||||
| chr9:94416570
|
T | C | 56 | a0001c0001t0001g0001a0001c0001t0001g0225a0001c0001t0001g0226others(53): Show | 58 | HG00323.hp2 HG00423.hp2 HG00438.hp2 others(55): Show |
intron_variant | MODIFIER | c.204+1317T>C | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 2/11 | chr9 | 94416570 | ||||||
| chr9:94416673
|
G | C | 1 | a0001c0001t0003g0147 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.204+1420G>C | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 2/11 | chr9 | 94416673 | ||||||
| chr9:94416784
|
G | T | 1 | a0001c0001t0003g0155 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.204+1531G>T | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 2/11 | chr9 | 94416784 | ||||||
| chr9:94416791
|
T | G | 1 | a0001c0001t0001g0229 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.204+1538T>G | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 2/11 | chr9 | 94416791 | ||||||
| chr9:94416827
|
T | C | 183 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0077others(180): Show | 187 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(184): Show |
intron_variant | MODIFIER | c.204+1574T>C | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 2/11 | chr9 | 94416827 | ||||||
| chr9:94416854
|
C | CA | 6 | a0001c0001t0002g0123a0001c0001t0002g0186a0001c0001t0002g0198others(3): Show | 6 | HG00408.hp1 HG04204.hp1 NA18948.hp2 others(3): Show |
intron_variant | MODIFIER | c.204+1617dupA | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr9 | 94416854 | |||||
| chr9:94416854
|
CA | C | 194 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0077others(191): Show | 198 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(195): Show |
intron_variant | MODIFIER | c.204+1617delA | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr9 | 94416854 | |||||
| chr9:94417106
|
T | G | 11 | a0001c0001t0006g0107a0001c0001t0006g0108a0001c0001t0006g0109others(8): Show | 11 | HG01243.hp2 HG02109.hp1 HG02280.hp2 others(8): Show |
intron_variant | MODIFIER | c.204+1853T>G | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 2/11 | chr9 | 94417106 | ||||||
| chr9:94417141
|
A | G | 1 | a0001c0001t0016g0025 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.204+1888A>G | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 2/11 | chr9 | 94417141 | ||||||
| chr9:94417344
|
T | C | 47 | a0001c0001t0002g0029a0001c0001t0002g0036a0001c0001t0002g0039others(44): Show | 47 | HG00597.hp1 HG00639.hp2 HG00642.hp1 others(44): Show |
intron_variant | MODIFIER | c.204+2091T>C | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 2/11 | chr9 | 94417344 | ||||||
| chr9:94417354
|
G | A | 1 | a0001c0001t0004g0060 | 1 | NA19004.hp1 | intron_variant | MODIFIER | c.204+2101G>A | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 2/11 | chr9 | 94417354 | ||||||
| chr9:94417433
|
C | T | 3 | a0001c0001t0002g0340a0001c0001t0002g0341a0001c0001t0002g0342 | 3 | HG01884.hp2 HG02886.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.204+2180C>T | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 2/11 | chr9 | 94417433 | ||||||
| chr9:94417456
|
A | C | 183 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0077others(180): Show | 187 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(184): Show |
intron_variant | MODIFIER | c.204+2203A>C | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 2/11 | chr9 | 94417456 | ||||||
| chr9:94417566
|
A | G | 183 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0077others(180): Show | 187 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(184): Show |
intron_variant | MODIFIER | c.204+2313A>G | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 2/11 | chr9 | 94417566 | ||||||
| chr9:94417666
|
T | C | 3 | a0001c0001t0002g0218a0001c0001t0002g0219a0001c0001t0002g0220 | 3 | HG02818.hp1 HG03209.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.204+2413T>C | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 2/11 | chr9 | 94417666 | ||||||
| chr9:94417688
|
A | G | 1 | a0001c0001t0008g0017 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.204+2435A>G | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 2/11 | chr9 | 94417688 | ||||||
| chr9:94417790
|
T | C | 11 | a0001c0001t0006g0107a0001c0001t0006g0108a0001c0001t0006g0109others(8): Show | 11 | HG01243.hp2 HG02109.hp1 HG02280.hp2 others(8): Show |
intron_variant | MODIFIER | c.204+2537T>C | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 2/11 | chr9 | 94417790 | ||||||
| chr9:94417808
|
C | T | 1 | a0001c0001t0016g0025 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.204+2555C>T | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 2/11 | chr9 | 94417808 | ||||||
| chr9:94417833
|
C | A | 32 | a0001c0001t0002g0315a0001c0001t0002g0316a0001c0001t0002g0317others(29): Show | 32 | HG00639.hp1 HG01109.hp2 HG01255.hp1 others(29): Show |
intron_variant | MODIFIER | c.204+2580C>A | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 2/11 | chr9 | 94417833 | ||||||
| chr9:94417849
|
T | TCCCGCCC others(3): Show |
1 | a0001c0001t0002g0333 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.204+2599_204+2600i others(12): Show |
MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr9 | 94417849 | |||||
| chr9:94417849
|
TCCCACCC others(4): Show |
T | 7 | a0001c0001t0002g0319a0001c0001t0002g0323a0001c0001t0002g0324others(4): Show | 7 | HG01256.hp2 HG02015.hp1 HG02723.hp2 others(4): Show |
intron_variant | MODIFIER | c.204+2600_204+2610d others(13): Show |
MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr9 | 94417849 | |||||
| chr9:94417849
|
TCCCACCC others(5): Show |
T | 1 | a0001c0001t0002g0334 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.204+2600_204+2611d others(14): Show |
MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr9 | 94417849 | |||||
| chr9:94417853
|
A | C | 8 | a0001c0001t0002g0321a0001c0001t0002g0326a0001c0001t0002g0327others(5): Show | 8 | HG01109.hp2 HG01496.hp2 HG02683.hp1 others(5): Show |
intron_variant | MODIFIER | c.204+2600A>C | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 2/11 | chr9 | 94417853 | ||||||
| chr9:94417853
|
ACCCCACC others(3): Show |
A | 3 | a0001c0001t0002g0320a0001c0001t0002g0330a0001c0001t0020g0332 | 3 | HG01255.hp1 HG02717.hp2 HG02896.hp2 |
intron_variant | MODIFIER | c.204+2605_204+2614d others(12): Show |
MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr9 | 94417853 | |||||
| chr9:94417858
|
A | C | 18 | a0001c0001t0002g0119a0001c0001t0002g0123a0001c0001t0002g0140others(15): Show | 18 | HG00639.hp1 HG01109.hp2 HG01496.hp2 others(15): Show |
intron_variant | MODIFIER | c.204+2605A>C | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 2/11 | chr9 | 94417858 | ||||||
| chr9:94417858
|
AC | A | 23 | a0001c0001t0002g0149a0001c0001t0002g0153a0001c0001t0002g0180others(20): Show | 23 | HG00408.hp1 HG00544.hp2 HG01517.hp2 others(20): Show |
intron_variant | MODIFIER | c.204+2623delC | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr9 | 94417858 | |||||
| chr9:94417858
|
ACCCCCC | A | 19 | a0001c0001t0001g0003a0001c0001t0001g0088a0001c0001t0001g0090others(16): Show | 20 | HG00140.hp2 HG00280.hp2 HG00544.hp1 others(17): Show |
intron_variant | MODIFIER | c.204+2618_204+2623d others(8): Show |
MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr9 | 94417858 | |||||
| chr9:94417858
|
ACCCCCCC | A | 20 | a0001c0001t0001g0081a0001c0001t0001g0082a0001c0001t0001g0084others(17): Show | 20 | HG00099.hp2 HG00733.hp2 HG01074.hp1 others(17): Show |
intron_variant | MODIFIER | c.204+2617_204+2623d others(9): Show |
MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr9 | 94417858 | |||||
| chr9:94417858
|
ACCCCCCC others(1): Show |
A | 25 | a0001c0001t0001g0236a0001c0001t0001g0257a0001c0001t0001g0266others(22): Show | 25 | HG00323.hp2 HG00673.hp1 HG01081.hp1 others(22): Show |
intron_variant | MODIFIER | c.204+2616_204+2623d others(10): Show |
MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr9 | 94417858 | |||||
| chr9:94417858
|
ACCCCCCC others(2): Show |
A | 133 | a0001c0001t0001g0001a0001c0001t0001g0225a0001c0001t0001g0226others(130): Show | 136 | HG00408.hp2 HG00423.hp1 HG00423.hp2 others(133): Show |
intron_variant | MODIFIER | c.204+2615_204+2623d others(11): Show |
MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr9 | 94417858 | |||||
| chr9:94417862
|
C | A | 1 | a0001c0001t0002g0219 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.204+2609C>A | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 2/11 | chr9 | 94417862 | ||||||
| chr9:94417864
|
C | G | 3 | a0001c0001t0002g0153a0001c0001t0003g0120a0001c0001t0003g0172 | 3 | HG00544.hp2 NA18747.hp1 NA18957.hp1 |
intron_variant | MODIFIER | c.204+2611C>G | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 2/11 | chr9 | 94417864 | ||||||
| chr9:94417872
|
C | A | 2 | a0001c0001t0002g0039a0001c0001t0002g0040 | 2 | HG01516.hp1 HG01517.hp1 |
intron_variant | MODIFIER | c.204+2619C>A | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 2/11 | chr9 | 94417872 | ||||||
| chr9:94417874
|
C | G | 10 | a0001c0001t0002g0180a0001c0001t0003g0124a0001c0001t0003g0160others(7): Show | 10 | HG00408.hp1 HG00621.hp2 HG02615.hp2 others(7): Show |
intron_variant | MODIFIER | c.204+2621C>G | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 2/11 | chr9 | 94417874 | ||||||
| chr9:94417917
|
C | T | 57 | a0001c0001t0002g0029a0001c0001t0002g0036a0001c0001t0002g0039others(54): Show | 58 | HG00597.hp1 HG00639.hp2 HG00642.hp1 others(55): Show |
intron_variant | MODIFIER | c.204+2664C>T | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 2/11 | chr9 | 94417917 | ||||||
| chr9:94417920
|
G | A | 1 | a0001c0001t0003g0205 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.204+2667G>A | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 2/11 | chr9 | 94417920 | ||||||
| chr9:94418002
|
T | G | 183 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0077others(180): Show | 187 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(184): Show |
intron_variant | MODIFIER | c.204+2749T>G | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 2/11 | chr9 | 94418002 | ||||||
| chr9:94418017
|
C | T | 1 | a0001c0001t0017g0022 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.204+2764C>T | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 2/11 | chr9 | 94418017 | ||||||
| chr9:94418048
|
C | T | 5 | a0001c0001t0008g0009a0001c0001t0008g0010a0001c0001t0008g0011others(2): Show | 5 | HG02818.hp2 HG02922.hp2 HG02976.hp2 others(2): Show |
intron_variant | MODIFIER | c.204+2795C>T | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 2/11 | chr9 | 94418048 | ||||||
| chr9:94418049
|
G | A | 3 | a0001c0001t0002g0218a0001c0001t0002g0219a0001c0001t0002g0220 | 3 | HG02818.hp1 HG03209.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.204+2796G>A | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 2/11 | chr9 | 94418049 | ||||||
| chr9:94418052
|
A | G | 216 | a0001c0001t0002g0004a0001c0001t0002g0029a0001c0001t0002g0036others(213): Show | 219 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(216): Show |
intron_variant | MODIFIER | c.204+2799A>G | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 2/11 | chr9 | 94418052 | ||||||
| chr9:94418107
|
C | T | 126 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0077others(123): Show | 129 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(126): Show |
intron_variant | MODIFIER | c.204+2854C>T | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 2/11 | chr9 | 94418107 | ||||||
| chr9:94418279
|
T | G | 56 | a0001c0001t0001g0001a0001c0001t0001g0225a0001c0001t0001g0226others(53): Show | 58 | HG00323.hp2 HG00423.hp2 HG00438.hp2 others(55): Show |
intron_variant | MODIFIER | c.204+3026T>G | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 2/11 | chr9 | 94418279 | ||||||
| chr9:94418287
|
G | T | 25 | a0001c0001t0001g0242a0001c0001t0001g0243a0001c0001t0001g0244others(22): Show | 25 | HG00408.hp2 HG00423.hp1 HG00438.hp1 others(22): Show |
intron_variant | MODIFIER | c.204+3034G>T | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 2/11 | chr9 | 94418287 | ||||||
| chr9:94418338
|
T | G | 1 | a0001c0002t0021g0216 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.204+3085T>G | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 2/11 | chr9 | 94418338 | ||||||
| chr9:94418361
|
A | G | 183 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0077others(180): Show | 187 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(184): Show |
intron_variant | MODIFIER | c.204+3108A>G | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 2/11 | chr9 | 94418361 | ||||||
| chr9:94418395
|
T | C | 46 | a0001c0001t0002g0029a0001c0001t0002g0036a0001c0001t0002g0039others(43): Show | 46 | HG00597.hp1 HG00639.hp2 HG00642.hp1 others(43): Show |
intron_variant | MODIFIER | c.204+3142T>C | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 2/11 | chr9 | 94418395 | ||||||
| chr9:94418424
|
C | T | 2 | a0001c0001t0002g0321a0001c0001t0002g0322 | 2 | HG00639.hp1 HG01109.hp2 |
intron_variant | MODIFIER | c.204+3171C>T | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 2/11 | chr9 | 94418424 | ||||||
| chr9:94418435
|
G | A | 1 | a0001c0001t0017g0022 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.204+3182G>A | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 2/11 | chr9 | 94418435 | ||||||
| chr9:94418443
|
C | T | 10 | a0001c0001t0008g0009a0001c0001t0008g0010a0001c0001t0008g0011others(7): Show | 10 | HG01081.hp1 HG02280.hp1 HG02559.hp1 others(7): Show |
intron_variant | MODIFIER | c.204+3190C>T | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 2/11 | chr9 | 94418443 | ||||||
| chr9:94418450
|
T | G | 1 | a0001c0001t0016g0025 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.204+3197T>G | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 2/11 | chr9 | 94418450 | ||||||
| chr9:94418537
|
G | T | 1 | a0001c0001t0003g0007 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.204+3284G>T | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 2/11 | chr9 | 94418537 | ||||||
| chr9:94418656
|
G | A | 5 | a0001c0002t0009g0209a0001c0002t0009g0211a0001c0002t0009g0212others(2): Show | 5 | HG00140.hp2 HG00741.hp2 HG02602.hp1 others(2): Show |
intron_variant | MODIFIER | c.204+3403G>A | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 2/11 | chr9 | 94418656 | ||||||
| chr9:94418687
|
C | T | 1 | a0001c0001t0003g0183 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.204+3434C>T | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 2/11 | chr9 | 94418687 | ||||||
| chr9:94418713
|
T | G | 1 | a0001c0001t0004g0038 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.204+3460T>G | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 2/11 | chr9 | 94418713 | ||||||
| chr9:94418720
|
A | G | 343 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0077others(340): Show | 349 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(346): Show |
intron_variant | MODIFIER | c.204+3467A>G | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 2/11 | chr9 | 94418720 | ||||||
| chr9:94418754
|
A | T | 57 | a0001c0001t0002g0029a0001c0001t0002g0036a0001c0001t0002g0039others(54): Show | 58 | HG00597.hp1 HG00639.hp2 HG00642.hp1 others(55): Show |
intron_variant | MODIFIER | c.204+3501A>T | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 2/11 | chr9 | 94418754 | ||||||
| chr9:94418757
|
C | CT | 22 | a0001c0001t0001g0077a0001c0001t0001g0078a0001c0001t0001g0079others(19): Show | 22 | HG00323.hp1 HG00408.hp1 HG00438.hp2 others(19): Show |
intron_variant | MODIFIER | c.204+3522dupT | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr9 | 94418757 | |||||
| chr9:94418757
|
CT | C | 56 | a0001c0001t0002g0029a0001c0001t0002g0036a0001c0001t0002g0039others(53): Show | 57 | HG00639.hp2 HG00642.hp1 HG01069.hp1 others(54): Show |
intron_variant | MODIFIER | c.204+3522delT | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr9 | 94418757 | |||||
| chr9:94418772
|
T | G | 2 | a0001c0001t0013g0023a0001c0001t0013g0024 | 2 | HG02040.hp2 HG02132.hp2 |
intron_variant | MODIFIER | c.204+3519T>G | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 2/11 | chr9 | 94418772 | ||||||
| chr9:94418773
|
T | C | 2 | a0001c0001t0002g0218a0001c0001t0002g0220 | 2 | HG02818.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.204+3520T>C | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 2/11 | chr9 | 94418773 | ||||||
| chr9:94418775
|
T | TC | 3 | a0001c0001t0008g0009a0001c0001t0008g0010a0001c0001t0008g0011 | 3 | HG02818.hp2 HG02922.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.204+3523dupC | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr9 | 94418775 | |||||
| chr9:94418775
|
T | TTC | 19 | a0001c0001t0001g0003a0001c0001t0001g0081a0001c0001t0001g0082others(16): Show | 20 | HG00099.hp2 HG00280.hp2 HG00642.hp2 others(17): Show |
intron_variant | MODIFIER | c.204+3522_204+3523i others(4): Show |
MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 2/11 | chr9 | 94418775 | ||||||
| chr9:94418919
|
C | T | 57 | a0001c0001t0002g0029a0001c0001t0002g0036a0001c0001t0002g0039others(54): Show | 58 | HG00597.hp1 HG00639.hp2 HG00642.hp1 others(55): Show |
intron_variant | MODIFIER | c.204+3666C>T | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 2/11 | chr9 | 94418919 | ||||||
| chr9:94419115
|
T | G | 3 | a0001c0001t0008g0009a0001c0001t0008g0010a0001c0001t0008g0011 | 3 | HG02818.hp2 HG02922.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.204+3862T>G | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 2/11 | chr9 | 94419115 | ||||||
| chr9:94419172
|
G | A | 25 | a0001c0001t0001g0242a0001c0001t0001g0243a0001c0001t0001g0244others(22): Show | 25 | HG00408.hp2 HG00423.hp1 HG00438.hp1 others(22): Show |
intron_variant | MODIFIER | c.204+3919G>A | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 2/11 | chr9 | 94419172 | ||||||
| chr9:94419275
|
G | A | 3 | a0001c0001t0002g0218a0001c0001t0002g0219a0001c0001t0002g0220 | 3 | HG02818.hp1 HG03209.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.204+4022G>A | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 2/11 | chr9 | 94419275 | ||||||
| chr9:94419298
|
C | CT | 123 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0077others(120): Show | 126 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(123): Show |
intron_variant | MODIFIER | c.204+4061dupT | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr9 | 94419298 | |||||
| chr9:94419298
|
CT | C | 63 | a0001c0001t0002g0029a0001c0001t0002g0036a0001c0001t0002g0039others(60): Show | 64 | HG00597.hp1 HG00639.hp1 HG00639.hp2 others(61): Show |
intron_variant | MODIFIER | c.204+4061delT | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr9 | 94419298 | |||||
| chr9:94419302
|
T | TC | 10 | a0001c0001t0008g0009a0001c0001t0008g0010a0001c0001t0008g0011others(7): Show | 10 | HG01081.hp1 HG02280.hp1 HG02559.hp1 others(7): Show |
intron_variant | MODIFIER | c.204+4049_204+4050i others(3): Show |
MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 2/11 | chr9 | 94419302 | ||||||
| chr9:94419369
|
C | T | 32 | a0001c0001t0002g0315a0001c0001t0002g0316a0001c0001t0002g0317others(29): Show | 32 | HG00639.hp1 HG01109.hp2 HG01255.hp1 others(29): Show |
intron_variant | MODIFIER | c.204+4116C>T | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 2/11 | chr9 | 94419369 | ||||||
| chr9:94419428
|
G | C | 2 | a0001c0001t0013g0023a0001c0001t0013g0024 | 2 | HG02040.hp2 HG02132.hp2 |
intron_variant | MODIFIER | c.204+4175G>C | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 2/11 | chr9 | 94419428 | ||||||
| chr9:94419442
|
C | T | 1 | a0001c0001t0001g0259 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.204+4189C>T | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 2/11 | chr9 | 94419442 | ||||||
| chr9:94419464
|
T | G | 2 | a0001c0001t0013g0023a0001c0001t0013g0024 | 2 | HG02040.hp2 HG02132.hp2 |
intron_variant | MODIFIER | c.204+4211T>G | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 2/11 | chr9 | 94419464 | ||||||
| chr9:94419464
|
T | TTTTTG | 11 | a0001c0001t0006g0107a0001c0001t0006g0108a0001c0001t0006g0109others(8): Show | 11 | HG01243.hp2 HG02109.hp1 HG02280.hp2 others(8): Show |
intron_variant | MODIFIER | c.204+4223_204+4227d others(7): Show |
MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr9 | 94419464 | |||||
| chr9:94419492
|
T | A | 183 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0077others(180): Show | 187 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(184): Show |
intron_variant | MODIFIER | c.204+4239T>A | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 2/11 | chr9 | 94419492 | ||||||
| chr9:94419512
|
A | G | 1 | a0001c0001t0002g0132 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.204+4259A>G | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 2/11 | chr9 | 94419512 | ||||||
| chr9:94419547
|
C | T | 1 | a0001c0001t0004g0058 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.204+4294C>T | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 2/11 | chr9 | 94419547 | ||||||
| chr9:94419549
|
C | G | 9 | a0001c0001t0007g0099a0001c0001t0007g0100a0001c0001t0007g0101others(6): Show | 9 | HG00544.hp1 HG01884.hp1 HG02630.hp1 others(6): Show |
intron_variant | MODIFIER | c.204+4296C>G | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 2/11 | chr9 | 94419549 | ||||||
| chr9:94419559
|
C | T | 1 | a0001c0001t0002g0036 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.204+4306C>T | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 2/11 | chr9 | 94419559 | ||||||
| chr9:94419698
|
C | A | 32 | a0001c0001t0002g0315a0001c0001t0002g0316a0001c0001t0002g0317others(29): Show | 32 | HG00639.hp1 HG01109.hp2 HG01255.hp1 others(29): Show |
intron_variant | MODIFIER | c.204+4445C>A | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 2/11 | chr9 | 94419698 | ||||||
| chr9:94419756
|
T | G | 1 | a0001c0001t0001g0233 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.204+4503T>G | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 2/11 | chr9 | 94419756 | ||||||
| chr9:94419980
|
T | C | 32 | a0001c0001t0002g0315a0001c0001t0002g0316a0001c0001t0002g0317others(29): Show | 32 | HG00639.hp1 HG01109.hp2 HG01255.hp1 others(29): Show |
intron_variant | MODIFIER | c.204+4727T>C | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 2/11 | chr9 | 94419980 | ||||||
| chr9:94420055
|
T | C | 183 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0077others(180): Show | 187 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(184): Show |
intron_variant | MODIFIER | c.204+4802T>C | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 2/11 | chr9 | 94420055 | ||||||
| chr9:94420357
|
G | C | 2 | a0001c0001t0007g0104a0001c0001t0007g0106 | 2 | HG02630.hp1 HG02895.hp1 |
intron_variant | MODIFIER | c.204+5104G>C | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 2/11 | chr9 | 94420357 | ||||||
| chr9:94420381
|
G | A | 246 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0077others(243): Show | 250 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(247): Show |
intron_variant | MODIFIER | c.204+5128G>A | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 2/11 | chr9 | 94420381 | ||||||
| chr9:94420539
|
G | T | 1 | a0001c0001t0002g0137 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.204+5286G>T | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 2/11 | chr9 | 94420539 | ||||||
| chr9:94420595
|
C | CT | 32 | a0001c0001t0001g0081a0001c0001t0001g0259a0001c0001t0001g0303others(29): Show | 32 | HG00639.hp1 HG01255.hp1 HG01256.hp2 others(29): Show |
intron_variant | MODIFIER | c.204+5357dupT | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr9 | 94420595 | |||||
| chr9:94420595
|
CT | C | 8 | a0001c0001t0001g0239a0001c0001t0002g0145a0001c0001t0003g0129others(5): Show | 8 | HG00558.hp1 HG01069.hp2 HG01070.hp1 others(5): Show |
intron_variant | MODIFIER | c.204+5357delT | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr9 | 94420595 | |||||
| chr9:94420623
|
A | T | 2 | a0001c0001t0003g0177a0001c0001t0003g0178 | 2 | HG01074.hp2 NA20752.hp1 |
intron_variant | MODIFIER | c.204+5370A>T | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 2/11 | chr9 | 94420623 | ||||||
| chr9:94420747
|
A | G | 1 | a0001c0001t0017g0022 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.204+5494A>G | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 2/11 | chr9 | 94420747 | ||||||
| chr9:94420823
|
C | A | 32 | a0001c0001t0002g0315a0001c0001t0002g0316a0001c0001t0002g0317others(29): Show | 32 | HG00639.hp1 HG01109.hp2 HG01255.hp1 others(29): Show |
intron_variant | MODIFIER | c.204+5570C>A | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 2/11 | chr9 | 94420823 | ||||||
| chr9:94420857
|
C | A | 9 | a0001c0001t0007g0099a0001c0001t0007g0100a0001c0001t0007g0101others(6): Show | 9 | HG00544.hp1 HG01884.hp1 HG02630.hp1 others(6): Show |
intron_variant | MODIFIER | c.204+5604C>A | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 2/11 | chr9 | 94420857 | ||||||
| chr9:94421071
|
T | C | 246 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0077others(243): Show | 250 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(247): Show |
intron_variant | MODIFIER | c.204+5818T>C | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 2/11 | chr9 | 94421071 | ||||||
| chr9:94421116
|
T | C | 1 | a0001c0001t0016g0025 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.204+5863T>C | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 2/11 | chr9 | 94421116 | ||||||
| chr9:94421132
|
G | GT | 183 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0077others(180): Show | 187 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(184): Show |
intron_variant | MODIFIER | c.204+5880dupT | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr9 | 94421132 | |||||
| chr9:94421392
|
G | A | 1 | a0001c0002t0009g0210 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.204+6139G>A | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 2/11 | chr9 | 94421392 | ||||||
| chr9:94421430
|
T | A | 1 | a0001c0001t0016g0025 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.204+6177T>A | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 2/11 | chr9 | 94421430 | ||||||
| chr9:94421784
|
G | A | 2 | a0001c0001t0002g0039a0001c0001t0002g0040 | 2 | HG01516.hp1 HG01517.hp1 |
intron_variant | MODIFIER | c.204+6531G>A | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 2/11 | chr9 | 94421784 | ||||||
| chr9:94421880
|
C | T | 5 | a0001c0001t0004g0035a0001c0001t0004g0037a0001c0001t0004g0038others(2): Show | 5 | HG02896.hp1 HG02970.hp1 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.204+6627C>T | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 2/11 | chr9 | 94421880 | ||||||
| chr9:94421930
|
C | A | 4 | a0001c0001t0001g0077a0001c0001t0001g0078a0001c0001t0001g0079others(1): Show | 4 | HG00323.hp1 HG01358.hp1 HG02559.hp2 others(1): Show |
intron_variant | MODIFIER | c.204+6677C>A | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 2/11 | chr9 | 94421930 | ||||||
| chr9:94422114
|
C | T | 1 | a0001c0001t0006g0111 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.204+6861C>T | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 2/11 | chr9 | 94422114 | ||||||
| chr9:94422399
|
A | G | 2 | a0001c0001t0001g0284a0001c0001t0001g0292 | 2 | HG00408.hp2 HG02040.hp1 |
intron_variant | MODIFIER | c.205-6790A>G | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 2/11 | chr9 | 94422399 | ||||||
| chr9:94422469
|
G | A | 1 | a0001c0001t0002g0128 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.205-6720G>A | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 2/11 | chr9 | 94422469 | ||||||
| chr9:94422481
|
G | C | 1 | a0001c0001t0002g0316 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.205-6708G>C | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 2/11 | chr9 | 94422481 | ||||||
| chr9:94422520
|
G | A | 1 | a0001c0001t0002g0141 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.205-6669G>A | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 2/11 | chr9 | 94422520 | ||||||
| chr9:94422545
|
A | G | 2 | a0001c0001t0001g0289a0001c0001t0001g0290 | 2 | HG02074.hp2 HG02083.hp1 |
intron_variant | MODIFIER | c.205-6644A>G | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 2/11 | chr9 | 94422545 | ||||||
| chr9:94422935
|
C | CT | 32 | a0001c0001t0002g0004a0001c0001t0002g0118a0001c0001t0002g0119others(29): Show | 33 | HG00099.hp1 HG00558.hp2 HG00741.hp1 others(30): Show |
intron_variant | MODIFIER | c.205-6239dupT | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr9 | 94422935 | |||||
| chr9:94422935
|
CT | C | 183 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0077others(180): Show | 187 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(184): Show |
intron_variant | MODIFIER | c.205-6239delT | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr9 | 94422935 | |||||
| chr9:94422943
|
T | C | 49 | a0001c0001t0002g0315a0001c0001t0002g0316a0001c0001t0002g0317others(46): Show | 49 | HG00140.hp2 HG00544.hp1 HG00639.hp1 others(46): Show |
intron_variant | MODIFIER | c.205-6246T>C | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 2/11 | chr9 | 94422943 | ||||||
| chr9:94422999
|
C | T | 1 | a0001c0001t0001g0080 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.205-6190C>T | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 2/11 | chr9 | 94422999 | ||||||
| chr9:94423018
|
T | C | 343 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0077others(340): Show | 349 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(346): Show |
intron_variant | MODIFIER | c.205-6171T>C | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 2/11 | chr9 | 94423018 | ||||||
| chr9:94423029
|
C | G | 2 | a0001c0001t0001g0088a0001c0001t0001g0092 | 2 | HG00099.hp2 HG01261.hp2 |
intron_variant | MODIFIER | c.205-6160C>G | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 2/11 | chr9 | 94423029 | ||||||
| chr9:94423055
|
G | A | 4 | a0001c0001t0001g0077a0001c0001t0001g0078a0001c0001t0001g0079others(1): Show | 4 | HG00323.hp1 HG01358.hp1 HG02559.hp2 others(1): Show |
intron_variant | MODIFIER | c.205-6134G>A | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 2/11 | chr9 | 94423055 | ||||||
| chr9:94423265
|
CT | C | 183 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0077others(180): Show | 187 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(184): Show |
intron_variant | MODIFIER | c.205-5909delT | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr9 | 94423265 | |||||
| chr9:94423267
|
T | C | 2 | a0001c0001t0008g0015a0001c0001t0023g0256 | 2 | HG01081.hp1 HG02135.hp2 |
intron_variant | MODIFIER | c.205-5922T>C | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 2/11 | chr9 | 94423267 | ||||||
| chr9:94423268
|
T | C | 123 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0077others(120): Show | 126 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(123): Show |
intron_variant | MODIFIER | c.205-5921T>C | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 2/11 | chr9 | 94423268 | ||||||
| chr9:94423269
|
T | C | 1 | a0001c0001t0001g0262 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.205-5920T>C | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 2/11 | chr9 | 94423269 | ||||||
| chr9:94423270
|
T | C | 2 | a0001c0001t0013g0023a0001c0001t0013g0024 | 2 | HG02040.hp2 HG02132.hp2 |
intron_variant | MODIFIER | c.205-5919T>C | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 2/11 | chr9 | 94423270 | ||||||
| chr9:94423290
|
C | T | 183 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0077others(180): Show | 187 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(184): Show |
intron_variant | MODIFIER | c.205-5899C>T | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 2/11 | chr9 | 94423290 | ||||||
| chr9:94423330
|
T | TG | 246 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0077others(243): Show | 250 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(247): Show |
intron_variant | MODIFIER | c.205-5859_205-5858i others(3): Show |
MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 2/11 | chr9 | 94423330 | ||||||
| chr9:94423415
|
G | T | 1 | a0001c0001t0003g0152 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.205-5774G>T | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 2/11 | chr9 | 94423415 | ||||||
| chr9:94423445
|
G | A | 1 | a0001c0001t0001g0265 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.205-5744G>A | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 2/11 | chr9 | 94423445 | ||||||
| chr9:94423670
|
C | A | 10 | a0001c0001t0008g0009a0001c0001t0008g0010a0001c0001t0008g0011others(7): Show | 10 | HG01081.hp1 HG02280.hp1 HG02559.hp1 others(7): Show |
intron_variant | MODIFIER | c.205-5519C>A | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 2/11 | chr9 | 94423670 | ||||||
| chr9:94423676
|
T | A | 32 | a0001c0001t0002g0315a0001c0001t0002g0316a0001c0001t0002g0317others(29): Show | 32 | HG00639.hp1 HG01109.hp2 HG01255.hp1 others(29): Show |
intron_variant | MODIFIER | c.205-5513T>A | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 2/11 | chr9 | 94423676 | ||||||
| chr9:94423942
|
CT | C | 46 | a0001c0001t0002g0029a0001c0001t0002g0036a0001c0001t0002g0039others(43): Show | 46 | HG00597.hp1 HG00639.hp2 HG00642.hp1 others(43): Show |
intron_variant | MODIFIER | c.205-5242delT | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr9 | 94423942 | |||||
| chr9:94423971
|
A | G | 4 | a0001c0001t0002g0130a0001c0001t0002g0137a0001c0001t0002g0188others(1): Show | 4 | NA18951.hp1 NA18967.hp1 NA18994.hp2 others(1): Show |
intron_variant | MODIFIER | c.205-5218A>G | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 2/11 | chr9 | 94423971 | ||||||
| chr9:94424135
|
G | A | 1 | a0001c0001t0001g0267 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.205-5054G>A | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 2/11 | chr9 | 94424135 | ||||||
| chr9:94424231
|
T | G | 11 | a0001c0001t0006g0107a0001c0001t0006g0108a0001c0001t0006g0109others(8): Show | 11 | HG01243.hp2 HG02109.hp1 HG02280.hp2 others(8): Show |
intron_variant | MODIFIER | c.205-4958T>G | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 2/11 | chr9 | 94424231 | ||||||
| chr9:94424242
|
C | CG | 24 | a0001c0001t0001g0077a0001c0001t0001g0078a0001c0001t0001g0079others(21): Show | 24 | HG00323.hp1 HG00544.hp1 HG01081.hp2 others(21): Show |
intron_variant | MODIFIER | c.205-4945dupG | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr9 | 94424242 | |||||
| chr9:94424245
|
A | C | 7 | a0001c0001t0005g0002a0001c0001t0005g0030a0001c0001t0005g0031others(4): Show | 8 | HG01069.hp1 HG01071.hp1 HG02615.hp2 others(5): Show |
intron_variant | MODIFIER | c.205-4944A>C | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 2/11 | chr9 | 94424245 | ||||||
| chr9:94424245
|
A | G | 148 | a0001c0001t0001g0003a0001c0001t0001g0077a0001c0001t0001g0078others(145): Show | 149 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(146): Show |
intron_variant | MODIFIER | c.205-4944A>G | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 2/11 | chr9 | 94424245 | ||||||
| chr9:94424245
|
A | T | 89 | a0001c0001t0001g0001a0001c0001t0001g0225a0001c0001t0001g0226others(86): Show | 91 | HG00323.hp2 HG00408.hp2 HG00423.hp1 others(88): Show |
intron_variant | MODIFIER | c.205-4944A>T | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 2/11 | chr9 | 94424245 | ||||||
| chr9:94424298
|
G | A | 183 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0077others(180): Show | 187 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(184): Show |
intron_variant | MODIFIER | c.205-4891G>A | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 2/11 | chr9 | 94424298 | ||||||
| chr9:94424496
|
A | C | 182 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0077others(179): Show | 186 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(183): Show |
intron_variant | MODIFIER | c.205-4693A>C | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 2/11 | chr9 | 94424496 | ||||||
| chr9:94424658
|
G | C | 9 | a0001c0001t0007g0099a0001c0001t0007g0100a0001c0001t0007g0101others(6): Show | 9 | HG00544.hp1 HG01884.hp1 HG02630.hp1 others(6): Show |
intron_variant | MODIFIER | c.205-4531G>C | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 2/11 | chr9 | 94424658 | ||||||
| chr9:94424664
|
A | G | 1 | a0001c0001t0002g0318 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.205-4525A>G | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 2/11 | chr9 | 94424664 | ||||||
| chr9:94424709
|
T | A | 4 | a0001c0001t0008g0009a0001c0001t0008g0010a0001c0001t0008g0011others(1): Show | 4 | HG02818.hp2 HG02922.hp2 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.205-4480T>A | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 2/11 | chr9 | 94424709 | ||||||
| chr9:94424717
|
T | C | 11 | a0001c0001t0001g0277a0001c0001t0008g0009a0001c0001t0008g0010others(8): Show | 11 | HG01081.hp1 HG01106.hp2 HG02280.hp1 others(8): Show |
intron_variant | MODIFIER | c.205-4472T>C | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 2/11 | chr9 | 94424717 | ||||||
| chr9:94424727
|
C | CT | 53 | a0001c0001t0002g0219a0001c0001t0002g0315a0001c0001t0002g0316others(50): Show | 53 | HG00140.hp2 HG00639.hp1 HG01109.hp2 others(50): Show |
intron_variant | MODIFIER | c.205-4439dupT | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr9 | 94424727 | |||||
| chr9:94424727
|
C | CTT | 15 | a0001c0001t0002g0218a0001c0001t0002g0220a0001c0001t0002g0333others(12): Show | 15 | HG00544.hp1 HG00741.hp2 HG01255.hp2 others(12): Show |
intron_variant | MODIFIER | c.205-4440_205-4439d others(4): Show |
MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr9 | 94424727 | |||||
| chr9:94424727
|
CT | C | 36 | a0001c0001t0002g0004a0001c0001t0002g0118a0001c0001t0002g0119others(33): Show | 37 | HG00099.hp1 HG00408.hp1 HG00558.hp2 others(34): Show |
intron_variant | MODIFIER | c.205-4439delT | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr9 | 94424727 | |||||
| chr9:94424727
|
CTTTTT | C | 57 | a0001c0001t0001g0229a0001c0001t0001g0272a0001c0001t0001g0310others(54): Show | 58 | HG00597.hp1 HG00639.hp2 HG00642.hp1 others(55): Show |
intron_variant | MODIFIER | c.205-4443_205-4439d others(7): Show |
MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr9 | 94424727 | |||||
| chr9:94424727
|
CTTTTTT | C | 121 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0077others(118): Show | 124 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(121): Show |
intron_variant | MODIFIER | c.205-4444_205-4439d others(8): Show |
MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr9 | 94424727 | |||||
| chr9:94424856
|
C | T | 1 | a0001c0001t0004g0035 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.205-4333C>T | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 2/11 | chr9 | 94424856 | ||||||
| chr9:94424857
|
G | A | 1 | a0001c0001t0003g0157 | 1 | HG01169.hp2 | intron_variant | MODIFIER | c.205-4332G>A | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 2/11 | chr9 | 94424857 | ||||||
| chr9:94424915
|
T | A | 20 | a0001c0001t0001g0003a0001c0001t0001g0081a0001c0001t0001g0082others(17): Show | 21 | HG00099.hp2 HG00280.hp2 HG00642.hp2 others(18): Show |
intron_variant | MODIFIER | c.205-4274T>A | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 2/11 | chr9 | 94424915 | ||||||
| chr9:94424916
|
T | A | 59 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0081others(56): Show | 62 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(59): Show |
intron_variant | MODIFIER | c.205-4273T>A | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 2/11 | chr9 | 94424916 | ||||||
| chr9:94424917
|
T | A | 111 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0081others(108): Show | 114 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(111): Show |
intron_variant | MODIFIER | c.205-4272T>A | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 2/11 | chr9 | 94424917 | ||||||
| chr9:94424918
|
T | A | 125 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0077others(122): Show | 128 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(125): Show |
intron_variant | MODIFIER | c.205-4271T>A | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 2/11 | chr9 | 94424918 | ||||||
| chr9:94424918
|
TA | T | 9 | a0001c0001t0007g0099a0001c0001t0007g0100a0001c0001t0007g0101others(6): Show | 9 | HG00544.hp1 HG01884.hp1 HG02630.hp1 others(6): Show |
intron_variant | MODIFIER | c.205-4268delA | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr9 | 94424918 | |||||
| chr9:94424919
|
A | T | 10 | a0001c0001t0002g0335a0001c0001t0006g0117a0001c0002t0009g0209others(7): Show | 10 | HG00140.hp2 HG00741.hp2 HG01255.hp2 others(7): Show |
intron_variant | MODIFIER | c.205-4270A>T | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 2/11 | chr9 | 94424919 | ||||||
| chr9:94424932
|
C | G | 246 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0077others(243): Show | 250 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(247): Show |
intron_variant | MODIFIER | c.205-4257C>G | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 2/11 | chr9 | 94424932 | ||||||
| chr9:94425038
|
A | G | 19 | a0001c0001t0001g0003a0001c0001t0001g0081a0001c0001t0001g0082others(16): Show | 20 | HG00099.hp2 HG00280.hp2 HG00642.hp2 others(17): Show |
intron_variant | MODIFIER | c.205-4151A>G | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 2/11 | chr9 | 94425038 | ||||||
| chr9:94425091
|
G | C | 218 | a0001c0001t0002g0004a0001c0001t0002g0029a0001c0001t0002g0036others(215): Show | 221 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(218): Show |
intron_variant | MODIFIER | c.205-4098G>C | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 2/11 | chr9 | 94425091 | ||||||
| chr9:94425145
|
A | C | 160 | a0001c0001t0002g0004a0001c0001t0002g0118a0001c0001t0002g0119others(157): Show | 162 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(159): Show |
intron_variant | MODIFIER | c.205-4044A>C | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 2/11 | chr9 | 94425145 | ||||||
| chr9:94425182
|
T | C | 1 | a0001c0001t0002g0339 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.205-4007T>C | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 2/11 | chr9 | 94425182 | ||||||
| chr9:94425204
|
T | G | 2 | a0001c0001t0008g0009a0001c0001t0008g0010 | 2 | HG02818.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.205-3985T>G | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 2/11 | chr9 | 94425204 | ||||||
| chr9:94425231
|
G | C | 57 | a0001c0001t0002g0029a0001c0001t0002g0036a0001c0001t0002g0039others(54): Show | 58 | HG00597.hp1 HG00639.hp2 HG00642.hp1 others(55): Show |
intron_variant | MODIFIER | c.205-3958G>C | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 2/11 | chr9 | 94425231 | ||||||
| chr9:94425253
|
G | A | 2 | a0001c0001t0013g0023a0001c0001t0013g0024 | 2 | HG02040.hp2 HG02132.hp2 |
intron_variant | MODIFIER | c.205-3936G>A | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 2/11 | chr9 | 94425253 | ||||||
| chr9:94425380
|
C | T | 7 | a0001c0001t0002g0326a0001c0001t0002g0327a0001c0001t0002g0328others(4): Show | 7 | HG02015.hp1 HG03834.hp1 NA18978.hp1 others(4): Show |
intron_variant | MODIFIER | c.205-3809C>T | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 2/11 | chr9 | 94425380 | ||||||
| chr9:94425723
|
TA | T | 3 | a0001c0001t0007g0099a0001c0001t0007g0100a0001c0001t0007g0105 | 3 | HG02922.hp1 HG03516.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.205-3464delA | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr9 | 94425723 | |||||
| chr9:94426077
|
C | A | 183 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0077others(180): Show | 187 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(184): Show |
intron_variant | MODIFIER | c.205-3112C>A | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 2/11 | chr9 | 94426077 | ||||||
| chr9:94426208
|
G | A | 89 | a0001c0001t0001g0001a0001c0001t0001g0225a0001c0001t0001g0226others(86): Show | 91 | HG00323.hp2 HG00408.hp2 HG00423.hp1 others(88): Show |
intron_variant | MODIFIER | c.205-2981G>A | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 2/11 | chr9 | 94426208 | ||||||
| chr9:94426268
|
A | G | 1 | a0001c0001t0008g0344 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.205-2921A>G | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 2/11 | chr9 | 94426268 | ||||||
| chr9:94426587
|
G | T | 32 | a0001c0001t0002g0315a0001c0001t0002g0316a0001c0001t0002g0317others(29): Show | 32 | HG00639.hp1 HG01109.hp2 HG01255.hp1 others(29): Show |
intron_variant | MODIFIER | c.205-2602G>T | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 2/11 | chr9 | 94426587 | ||||||
| chr9:94426738
|
A | AT | 8 | a0001c0001t0001g0269a0001c0001t0001g0277a0001c0001t0001g0278others(5): Show | 8 | HG00408.hp2 HG00438.hp1 HG01106.hp2 others(5): Show |
intron_variant | MODIFIER | c.205-2444dupT | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr9 | 94426738 | |||||
| chr9:94426757
|
CATTTT | C | 53 | a0001c0001t0002g0029a0001c0001t0002g0036a0001c0001t0002g0039others(50): Show | 54 | HG00597.hp1 HG00639.hp2 HG00642.hp1 others(51): Show |
intron_variant | MODIFIER | c.205-2424_205-2420d others(7): Show |
MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr9 | 94426757 | |||||
| chr9:94427190
|
T | C | 125 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0077others(122): Show | 128 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(125): Show |
intron_variant | MODIFIER | c.205-1999T>C | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 2/11 | chr9 | 94427190 | ||||||
| chr9:94427582
|
T | C | 246 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0077others(243): Show | 250 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(247): Show |
intron_variant | MODIFIER | c.205-1607T>C | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 2/11 | chr9 | 94427582 | ||||||
| chr9:94427619
|
C | T | 1 | a0001c0001t0004g0061 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.205-1570C>T | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 2/11 | chr9 | 94427619 | ||||||
| chr9:94427662
|
G | A | 4 | a0001c0001t0001g0077a0001c0001t0001g0078a0001c0001t0001g0079others(1): Show | 4 | HG00323.hp1 HG01358.hp1 HG02559.hp2 others(1): Show |
intron_variant | MODIFIER | c.205-1527G>A | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 2/11 | chr9 | 94427662 | ||||||
| chr9:94427692
|
A | G | 5 | a0001c0001t0001g0001a0001c0001t0001g0271a0001c0001t0001g0283others(2): Show | 7 | NA18944.hp2 NA18950.hp1 NA18967.hp2 others(4): Show |
intron_variant | MODIFIER | c.205-1497A>G | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 2/11 | chr9 | 94427692 | ||||||
| chr9:94427768
|
T | A | 2 | a0001c0001t0013g0023a0001c0001t0013g0024 | 2 | HG02040.hp2 HG02132.hp2 |
intron_variant | MODIFIER | c.205-1421T>A | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 2/11 | chr9 | 94427768 | ||||||
| chr9:94427798
|
G | A | 1 | a0001c0001t0001g0255 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.205-1391G>A | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 2/11 | chr9 | 94427798 | ||||||
| chr9:94427852
|
A | G | 183 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0077others(180): Show | 187 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(184): Show |
intron_variant | MODIFIER | c.205-1337A>G | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 2/11 | chr9 | 94427852 | ||||||
| chr9:94427976
|
G | T | 1 | a0001c0001t0004g0070 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.205-1213G>T | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 2/11 | chr9 | 94427976 | ||||||
| chr9:94428039
|
C | A | 1 | a0001c0001t0002g0004 | 2 | HG02083.hp2 NA19080.hp2 |
intron_variant | MODIFIER | c.205-1150C>A | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 2/11 | chr9 | 94428039 | ||||||
| chr9:94428139
|
G | T | 2 | a0001c0001t0008g0009a0001c0001t0008g0010 | 2 | HG02818.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.205-1050G>T | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 2/11 | chr9 | 94428139 | ||||||
| chr9:94428244
|
A | C | 57 | a0001c0001t0002g0029a0001c0001t0002g0036a0001c0001t0002g0039others(54): Show | 58 | HG00597.hp1 HG00639.hp2 HG00642.hp1 others(55): Show |
intron_variant | MODIFIER | c.205-945A>C | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 2/11 | chr9 | 94428244 | ||||||
| chr9:94428370
|
A | G | 1 | a0001c0001t0008g0012 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.205-819A>G | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 2/11 | chr9 | 94428370 | ||||||
| chr9:94428380
|
G | A | 278 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0077others(275): Show | 283 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(280): Show |
intron_variant | MODIFIER | c.205-809G>A | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 2/11 | chr9 | 94428380 | ||||||
| chr9:94428421
|
C | A | 1 | a0001c0001t0017g0022 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.205-768C>A | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 2/11 | chr9 | 94428421 | ||||||
| chr9:94428488
|
G | A | 3 | a0001c0001t0001g0304a0001c0001t0001g0305a0001c0001t0001g0306 | 3 | HG02451.hp2 HG03471.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.205-701G>A | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 2/11 | chr9 | 94428488 | ||||||
| chr9:94428590
|
A | AC | 28 | a0001c0001t0001g0079a0001c0001t0001g0236a0001c0001t0001g0272others(25): Show | 28 | HG01192.hp2 HG01884.hp1 HG01884.hp2 others(25): Show |
intron_variant | MODIFIER | c.205-589dupC | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr9 | 94428590 | |||||
| chr9:94428590
|
AC | A | 71 | a0001c0001t0001g0003a0001c0001t0001g0081a0001c0001t0001g0082others(68): Show | 73 | HG00099.hp2 HG00280.hp2 HG00597.hp1 others(70): Show |
intron_variant | MODIFIER | c.205-589delC | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr9 | 94428590 | |||||
| chr9:94428600
|
CT | C | 42 | a0001c0001t0001g0229a0001c0001t0001g0242a0001c0001t0001g0243others(39): Show | 42 | HG00408.hp2 HG00438.hp1 HG01081.hp2 others(39): Show |
intron_variant | MODIFIER | c.205-577delT | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr9 | 94428600 | |||||
| chr9:94428601
|
T | C | 57 | a0001c0001t0001g0001a0001c0001t0001g0225a0001c0001t0001g0226others(54): Show | 59 | HG00323.hp2 HG00423.hp2 HG00438.hp2 others(56): Show |
intron_variant | MODIFIER | c.205-588T>C | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 2/11 | chr9 | 94428601 | ||||||
| chr9:94428602
|
T | C | 8 | a0001c0001t0007g0099a0001c0001t0007g0100a0001c0001t0007g0101others(5): Show | 8 | HG00544.hp1 HG01884.hp1 HG02630.hp1 others(5): Show |
intron_variant | MODIFIER | c.205-587T>C | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 2/11 | chr9 | 94428602 | ||||||
| chr9:94428815
|
G | C | 1 | a0001c0001t0002g0137 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.205-374G>C | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 2/11 | chr9 | 94428815 | ||||||
| chr9:94428959
|
A | G | 10 | a0001c0001t0008g0009a0001c0001t0008g0010a0001c0001t0008g0011others(7): Show | 10 | HG01081.hp1 HG02280.hp1 HG02559.hp1 others(7): Show |
intron_variant | MODIFIER | c.205-230A>G | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 2/11 | chr9 | 94428959 | ||||||
| chr9:94428992
|
A | G | 1 | a0001c0001t0003g0147 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.205-197A>G | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 2/11 | chr9 | 94428992 | ||||||
| chr9:94429097
|
G | A | 57 | a0001c0001t0002g0029a0001c0001t0002g0036a0001c0001t0002g0039others(54): Show | 58 | HG00597.hp1 HG00639.hp2 HG00642.hp1 others(55): Show |
intron_variant | MODIFIER | c.205-92G>A | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 2/11 | chr9 | 94429097 | ||||||
| chr9:94429336
|
T | C | 1 | a0001c0001t0008g0014 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.267+85T>C | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 3/11 | chr9 | 94429336 | ||||||
| chr9:94429428
|
G | C | 1 | a0001c0001t0001g0301 | 1 | NA18972.hp2 | intron_variant | MODIFIER | c.267+177G>C | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 3/11 | chr9 | 94429428 | ||||||
| chr9:94429578
|
A | T | 183 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0077others(180): Show | 187 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(184): Show |
intron_variant | MODIFIER | c.267+327A>T | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 3/11 | chr9 | 94429578 | ||||||
| chr9:94429734
|
C | A | 1 | a0001c0001t0002g0123 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.267+483C>A | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 3/11 | chr9 | 94429734 | ||||||
| chr9:94429736
|
G | C | 1 | a0001c0001t0002g0123 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.267+485G>C | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 3/11 | chr9 | 94429736 | ||||||
| chr9:94429737
|
T | G | 1 | a0001c0001t0002g0123 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.267+486T>G | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 3/11 | chr9 | 94429737 | ||||||
| chr9:94429909
|
A | AT | 21 | a0001c0001t0002g0316a0001c0001t0002g0318a0001c0001t0002g0319others(18): Show | 21 | HG00639.hp1 HG01109.hp2 HG01256.hp2 others(18): Show |
intron_variant | MODIFIER | c.267+672dupT | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr9 | 94429909 | |||||
| chr9:94429909
|
A | ATT | 51 | a0001c0001t0002g0029a0001c0001t0002g0036a0001c0001t0002g0039others(48): Show | 52 | HG00597.hp1 HG00639.hp2 HG00642.hp1 others(49): Show |
intron_variant | MODIFIER | c.267+671_267+672dup others(2): Show |
MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr9 | 94429909 | |||||
| chr9:94429909
|
A | T | 1 | a0001c0001t0003g0170 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.267+658A>T | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 3/11 | chr9 | 94429909 | ||||||
| chr9:94429912
|
T | A | 89 | a0001c0001t0001g0001a0001c0001t0001g0225a0001c0001t0001g0226others(86): Show | 91 | HG00323.hp2 HG00408.hp2 HG00423.hp1 others(88): Show |
intron_variant | MODIFIER | c.267+661T>A | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 3/11 | chr9 | 94429912 | ||||||
| chr9:94429914
|
T | A | 15 | a0001c0001t0002g0218a0001c0001t0002g0219a0001c0001t0002g0220others(12): Show | 15 | HG01243.hp2 HG02109.hp1 HG02280.hp2 others(12): Show |
intron_variant | MODIFIER | c.267+663T>A | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 3/11 | chr9 | 94429914 | ||||||
| chr9:94429929
|
G | A | 60 | a0001c0001t0002g0315a0001c0001t0002g0316a0001c0001t0002g0317others(57): Show | 60 | HG00140.hp2 HG00544.hp1 HG00639.hp1 others(57): Show |
intron_variant | MODIFIER | c.267+678G>A | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 3/11 | chr9 | 94429929 | ||||||
| chr9:94429992
|
C | T | 1 | a0001c0001t0001g0084 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.267+741C>T | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 3/11 | chr9 | 94429992 | ||||||
| chr9:94430157
|
C | T | 183 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0077others(180): Show | 187 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(184): Show |
intron_variant | MODIFIER | c.267+906C>T | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 3/11 | chr9 | 94430157 | ||||||
| chr9:94430161
|
C | A | 1 | a0001c0001t0002g0186 | 1 | NA18997.hp2 | intron_variant | MODIFIER | c.267+910C>A | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 3/11 | chr9 | 94430161 | ||||||
| chr9:94430221
|
TA | T | 4 | a0001c0001t0005g0018a0001c0001t0005g0019a0001c0001t0005g0020others(1): Show | 4 | HG01081.hp2 HG01109.hp1 HG02486.hp2 others(1): Show |
intron_variant | MODIFIER | c.267+972delA | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr9 | 94430221 | |||||
| chr9:94430223
|
A | AT | 23 | a0001c0001t0001g0090a0001c0001t0001g0094a0001c0001t0001g0271others(20): Show | 23 | HG01243.hp2 HG01496.hp2 HG02055.hp1 others(20): Show |
intron_variant | MODIFIER | c.267+989dupT | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr9 | 94430223 | |||||
| chr9:94430223
|
AT | A | 75 | a0001c0001t0001g0233a0001c0001t0001g0242a0001c0001t0002g0029others(72): Show | 76 | HG00597.hp1 HG00639.hp2 HG00642.hp1 others(73): Show |
intron_variant | MODIFIER | c.267+989delT | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr9 | 94430223 | |||||
| chr9:94430325
|
T | C | 246 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0077others(243): Show | 250 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(247): Show |
intron_variant | MODIFIER | c.267+1074T>C | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 3/11 | chr9 | 94430325 | ||||||
| chr9:94430424
|
T | G | 1 | a0001c0002t0021g0216 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.267+1173T>G | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 3/11 | chr9 | 94430424 | ||||||
| chr9:94430443
|
G | A | 89 | a0001c0001t0001g0001a0001c0001t0001g0225a0001c0001t0001g0226others(86): Show | 91 | HG00323.hp2 HG00408.hp2 HG00423.hp1 others(88): Show |
intron_variant | MODIFIER | c.267+1192G>A | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 3/11 | chr9 | 94430443 | ||||||
| chr9:94430472
|
C | T | 3 | a0001c0001t0001g0274a0001c0001t0001g0302a0002c0004t0001g0299 | 3 | HG02165.hp2 HG02293.hp2 NA18975.hp2 |
intron_variant | MODIFIER | c.267+1221C>T | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 3/11 | chr9 | 94430472 | ||||||
| chr9:94430476
|
G | A | 3 | a0001c0001t0002g0218a0001c0001t0002g0219a0001c0001t0002g0220 | 3 | HG02818.hp1 HG03209.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.267+1225G>A | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 3/11 | chr9 | 94430476 | ||||||
| chr9:94430650
|
C | T | 1 | a0001c0001t0001g0096 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.267+1399C>T | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 3/11 | chr9 | 94430650 | ||||||
| chr9:94430662
|
C | G | 8 | a0001c0002t0009g0209a0001c0002t0009g0210a0001c0002t0009g0211others(5): Show | 8 | HG00140.hp2 HG00741.hp2 HG01255.hp2 others(5): Show |
intron_variant | MODIFIER | c.267+1411C>G | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 3/11 | chr9 | 94430662 | ||||||
| chr9:94430787
|
C | T | 57 | a0001c0001t0002g0029a0001c0001t0002g0036a0001c0001t0002g0039others(54): Show | 58 | HG00597.hp1 HG00639.hp2 HG00642.hp1 others(55): Show |
intron_variant | MODIFIER | c.267+1536C>T | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 3/11 | chr9 | 94430787 | ||||||
| chr9:94430856
|
G | A | 19 | a0001c0001t0001g0003a0001c0001t0001g0081a0001c0001t0001g0082others(16): Show | 20 | HG00099.hp2 HG00280.hp2 HG00642.hp2 others(17): Show |
intron_variant | MODIFIER | c.267+1605G>A | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 3/11 | chr9 | 94430856 | ||||||
| chr9:94430888
|
A | G | 246 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0077others(243): Show | 250 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(247): Show |
intron_variant | MODIFIER | c.267+1637A>G | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 3/11 | chr9 | 94430888 | ||||||
| chr9:94430920
|
T | C | 5 | a0001c0001t0001g0230a0001c0001t0001g0266a0001c0001t0001g0267others(2): Show | 5 | HG00438.hp2 HG00673.hp1 NA18970.hp2 others(2): Show |
intron_variant | MODIFIER | c.267+1669T>C | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 3/11 | chr9 | 94430920 | ||||||
| chr9:94430921
|
A | C | 1 | a0001c0001t0004g0035 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.267+1670A>C | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 3/11 | chr9 | 94430921 | ||||||
| chr9:94430932
|
T | A | 1 | a0001c0001t0002g0123 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.267+1681T>A | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 3/11 | chr9 | 94430932 | ||||||
| chr9:94431050
|
C | T | 2 | a0001c0001t0003g0206a0001c0001t0003g0207 | 2 | NA18968.hp1 NA19083.hp2 |
intron_variant | MODIFIER | c.267+1799C>T | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 3/11 | chr9 | 94431050 | ||||||
| chr9:94431051
|
G | A | 89 | a0001c0001t0001g0001a0001c0001t0001g0225a0001c0001t0001g0226others(86): Show | 91 | HG00323.hp2 HG00408.hp2 HG00423.hp1 others(88): Show |
intron_variant | MODIFIER | c.267+1800G>A | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 3/11 | chr9 | 94431051 | ||||||
| chr9:94431172
|
T | G | 183 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0077others(180): Show | 187 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(184): Show |
intron_variant | MODIFIER | c.267+1921T>G | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 3/11 | chr9 | 94431172 | ||||||
| chr9:94431271
|
C | T | 17 | a0001c0001t0002g0153a0001c0001t0002g0180a0001c0001t0003g0120others(14): Show | 17 | HG00408.hp1 HG00544.hp2 HG00621.hp2 others(14): Show |
intron_variant | MODIFIER | c.267+2020C>T | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 3/11 | chr9 | 94431271 | ||||||
| chr9:94431312
|
CA | C | 23 | a0001c0001t0001g0003a0001c0001t0001g0077a0001c0001t0001g0078others(20): Show | 24 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(21): Show |
intron_variant | MODIFIER | c.267+2077delA | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr9 | 94431312 | |||||
| chr9:94431321
|
A | G | 1 | a0001c0001t0002g0141 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.267+2070A>G | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 3/11 | chr9 | 94431321 | ||||||
| chr9:94431329
|
T | A | 3 | a0001c0001t0002g0218a0001c0001t0002g0219a0001c0001t0002g0220 | 3 | HG02818.hp1 HG03209.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.267+2078T>A | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 3/11 | chr9 | 94431329 | ||||||
| chr9:94431369
|
G | A | 1 | a0001c0001t0003g0221 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.267+2118G>A | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 3/11 | chr9 | 94431369 | ||||||
| chr9:94431430
|
A | G | 1 | a0001c0001t0003g0171 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.267+2179A>G | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 3/11 | chr9 | 94431430 | ||||||
| chr9:94431516
|
C | CT | 51 | a0001c0001t0002g0029a0001c0001t0002g0036a0001c0001t0002g0039others(48): Show | 51 | HG00597.hp1 HG00639.hp2 HG00642.hp1 others(48): Show |
intron_variant | MODIFIER | c.267+2275dupT | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr9 | 94431516 | |||||
| chr9:94431576
|
A | T | 1 | a0001c0001t0001g0301 | 1 | NA18972.hp2 | intron_variant | MODIFIER | c.267+2325A>T | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 3/11 | chr9 | 94431576 | ||||||
| chr9:94431719
|
A | G | 41 | a0001c0001t0002g0029a0001c0001t0002g0036a0001c0001t0002g0039others(38): Show | 41 | HG00597.hp1 HG00639.hp2 HG00642.hp1 others(38): Show |
intron_variant | MODIFIER | c.267+2468A>G | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 3/11 | chr9 | 94431719 | ||||||
| chr9:94431752
|
A | AC | 32 | a0001c0001t0002g0315a0001c0001t0002g0316a0001c0001t0002g0317others(29): Show | 32 | HG00639.hp1 HG01109.hp2 HG01255.hp1 others(29): Show |
intron_variant | MODIFIER | c.267+2506dupC | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr9 | 94431752 | |||||
| chr9:94431753
|
C | A | 1 | a0001c0001t0017g0022 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.267+2502C>A | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 3/11 | chr9 | 94431753 | ||||||
| chr9:94431941
|
T | C | 1 | a0001c0001t0004g0069 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.267+2690T>C | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 3/11 | chr9 | 94431941 | ||||||
| chr9:94432032
|
C | T | 1 | a0001c0001t0016g0025 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.267+2781C>T | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 3/11 | chr9 | 94432032 | ||||||
| chr9:94432095
|
G | A | 183 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0077others(180): Show | 187 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(184): Show |
intron_variant | MODIFIER | c.267+2844G>A | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 3/11 | chr9 | 94432095 | ||||||
| chr9:94432194
|
A | G | 1 | a0001c0001t0004g0042 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.267+2943A>G | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 3/11 | chr9 | 94432194 | ||||||
| chr9:94432238
|
C | G | 2 | a0001c0001t0001g0285a0001c0001t0001g0286 | 2 | HG02109.hp2 HG02258.hp2 |
intron_variant | MODIFIER | c.267+2987C>G | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 3/11 | chr9 | 94432238 | ||||||
| chr9:94432252
|
G | A | 92 | a0001c0001t0001g0001a0001c0001t0001g0225a0001c0001t0001g0226others(89): Show | 94 | HG00323.hp2 HG00408.hp2 HG00423.hp1 others(91): Show |
intron_variant | MODIFIER | c.267+3001G>A | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 3/11 | chr9 | 94432252 | ||||||
| chr9:94432378
|
T | A | 1 | a0001c0001t0003g0007 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.267+3127T>A | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 3/11 | chr9 | 94432378 | ||||||
| chr9:94432399
|
C | G | 1 | a0001c0001t0005g0018 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.267+3148C>G | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 3/11 | chr9 | 94432399 | ||||||
| chr9:94432454
|
C | G | 1 | a0001c0001t0008g0344 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.267+3203C>G | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 3/11 | chr9 | 94432454 | ||||||
| chr9:94432480
|
A | G | 19 | a0001c0001t0002g0318a0001c0001t0002g0319a0001c0001t0002g0321others(16): Show | 19 | HG00639.hp1 HG01109.hp2 HG01256.hp2 others(16): Show |
intron_variant | MODIFIER | c.267+3229A>G | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 3/11 | chr9 | 94432480 | ||||||
| chr9:94432710
|
G | C | 89 | a0001c0001t0001g0001a0001c0001t0001g0225a0001c0001t0001g0226others(86): Show | 91 | HG00323.hp2 HG00408.hp2 HG00423.hp1 others(88): Show |
intron_variant | MODIFIER | c.267+3459G>C | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 3/11 | chr9 | 94432710 | ||||||
| chr9:94432837
|
C | G | 89 | a0001c0001t0001g0001a0001c0001t0001g0225a0001c0001t0001g0226others(86): Show | 91 | HG00323.hp2 HG00408.hp2 HG00423.hp1 others(88): Show |
intron_variant | MODIFIER | c.267+3586C>G | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 3/11 | chr9 | 94432837 | ||||||
| chr9:94432852
|
C | T | 4 | a0001c0001t0005g0018a0001c0001t0005g0019a0001c0001t0005g0020others(1): Show | 4 | HG01081.hp2 HG01109.hp1 HG02486.hp2 others(1): Show |
intron_variant | MODIFIER | c.267+3601C>T | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 3/11 | chr9 | 94432852 | ||||||
| chr9:94432997
|
G | A | 1 | a0001c0001t0002g0140 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.267+3746G>A | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 3/11 | chr9 | 94432997 | ||||||
| chr9:94433031
|
T | C | 57 | a0001c0001t0002g0029a0001c0001t0002g0036a0001c0001t0002g0039others(54): Show | 58 | HG00597.hp1 HG00639.hp2 HG00642.hp1 others(55): Show |
intron_variant | MODIFIER | c.267+3780T>C | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 3/11 | chr9 | 94433031 | ||||||
| chr9:94433035
|
G | A | 1 | a0001c0001t0003g0181 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.267+3784G>A | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 3/11 | chr9 | 94433035 | ||||||
| chr9:94433134
|
CTG | C | 57 | a0001c0001t0002g0029a0001c0001t0002g0036a0001c0001t0002g0039others(54): Show | 58 | HG00597.hp1 HG00639.hp2 HG00642.hp1 others(55): Show |
intron_variant | MODIFIER | c.267+3884_267+3885d others(4): Show |
MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 3/11 | chr9 | 94433134 | ||||||
| chr9:94433251
|
C | T | 10 | a0001c0001t0008g0009a0001c0001t0008g0010a0001c0001t0008g0011others(7): Show | 10 | HG01081.hp1 HG02280.hp1 HG02559.hp1 others(7): Show |
intron_variant | MODIFIER | c.267+4000C>T | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 3/11 | chr9 | 94433251 | ||||||
| chr9:94433347
|
A | G | 4 | a0001c0001t0003g0176a0001c0001t0003g0177a0001c0001t0003g0178others(1): Show | 4 | HG00140.hp1 HG01074.hp2 HG02602.hp2 others(1): Show |
intron_variant | MODIFIER | c.267+4096A>G | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 3/11 | chr9 | 94433347 | ||||||
| chr9:94433372
|
T | TA | 91 | a0001c0001t0001g0001a0001c0001t0001g0225a0001c0001t0001g0226others(88): Show | 93 | HG00323.hp2 HG00408.hp2 HG00423.hp1 others(90): Show |
intron_variant | MODIFIER | c.267+4129dupA | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr9 | 94433372 | |||||
| chr9:94433381
|
G | A | 245 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0077others(242): Show | 249 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(246): Show |
intron_variant | MODIFIER | c.267+4130G>A | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 3/11 | chr9 | 94433381 | ||||||
| chr9:94433394
|
C | T | 32 | a0001c0001t0002g0315a0001c0001t0002g0316a0001c0001t0002g0317others(29): Show | 32 | HG00639.hp1 HG01109.hp2 HG01255.hp1 others(29): Show |
intron_variant | MODIFIER | c.267+4143C>T | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 3/11 | chr9 | 94433394 | ||||||
| chr9:94433491
|
C | T | 3 | a0001c0001t0002g0218a0001c0001t0002g0219a0001c0001t0002g0220 | 3 | HG02818.hp1 HG03209.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.267+4240C>T | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 3/11 | chr9 | 94433491 | ||||||
| chr9:94433539
|
G | A | 1 | a0001c0001t0016g0025 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.267+4288G>A | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 3/11 | chr9 | 94433539 | ||||||
| chr9:94433612
|
A | G | 9 | a0001c0001t0007g0099a0001c0001t0007g0100a0001c0001t0007g0101others(6): Show | 9 | HG00544.hp1 HG01884.hp1 HG02630.hp1 others(6): Show |
intron_variant | MODIFIER | c.267+4361A>G | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 3/11 | chr9 | 94433612 | ||||||
| chr9:94433617
|
C | T | 9 | a0001c0001t0007g0099a0001c0001t0007g0100a0001c0001t0007g0101others(6): Show | 9 | HG00544.hp1 HG01884.hp1 HG02630.hp1 others(6): Show |
intron_variant | MODIFIER | c.267+4366C>T | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 3/11 | chr9 | 94433617 | ||||||
| chr9:94433697
|
T | A | 19 | a0001c0001t0001g0003a0001c0001t0001g0081a0001c0001t0001g0082others(16): Show | 20 | HG00099.hp2 HG00280.hp2 HG00642.hp2 others(17): Show |
intron_variant | MODIFIER | c.267+4446T>A | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 3/11 | chr9 | 94433697 | ||||||
| chr9:94433950
|
A | G | 1 | a0001c0001t0001g0233 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.268-4451A>G | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 3/11 | chr9 | 94433950 | ||||||
| chr9:94434084
|
A | G | 2 | a0001c0001t0001g0089a0001c0001t0001g0095 | 2 | HG01167.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.268-4317A>G | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 3/11 | chr9 | 94434084 | ||||||
| chr9:94434475
|
C | A | 1 | a0001c0001t0001g0302 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.268-3926C>A | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 3/11 | chr9 | 94434475 | ||||||
| chr9:94434479
|
G | A | 1 | a0001c0001t0001g0260 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.268-3922G>A | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 3/11 | chr9 | 94434479 | ||||||
| chr9:94434505
|
C | T | 9 | a0001c0001t0007g0099a0001c0001t0007g0100a0001c0001t0007g0101others(6): Show | 9 | HG00544.hp1 HG01884.hp1 HG02630.hp1 others(6): Show |
intron_variant | MODIFIER | c.268-3896C>T | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 3/11 | chr9 | 94434505 | ||||||
| chr9:94434560
|
C | T | 1 | a0001c0001t0001g0278 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.268-3841C>T | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 3/11 | chr9 | 94434560 | ||||||
| chr9:94434580
|
G | T | 1 | a0001c0001t0017g0022 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.268-3821G>T | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 3/11 | chr9 | 94434580 | ||||||
| chr9:94434605
|
G | A | 2 | a0001c0001t0001g0285a0001c0001t0001g0286 | 2 | HG02109.hp2 HG02258.hp2 |
intron_variant | MODIFIER | c.268-3796G>A | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 3/11 | chr9 | 94434605 | ||||||
| chr9:94434697
|
A | G | 125 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0077others(122): Show | 128 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(125): Show |
intron_variant | MODIFIER | c.268-3704A>G | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 3/11 | chr9 | 94434697 | ||||||
| chr9:94434708
|
C | A | 9 | a0001c0001t0007g0099a0001c0001t0007g0100a0001c0001t0007g0101others(6): Show | 9 | HG00544.hp1 HG01884.hp1 HG02630.hp1 others(6): Show |
intron_variant | MODIFIER | c.268-3693C>A | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 3/11 | chr9 | 94434708 | ||||||
| chr9:94434728
|
T | C | 3 | a0001c0001t0001g0304a0001c0001t0001g0305a0001c0001t0001g0306 | 3 | HG02451.hp2 HG03471.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.268-3673T>C | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 3/11 | chr9 | 94434728 | ||||||
| chr9:94434987
|
A | G | 1 | a0001c0001t0001g0253 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.268-3414A>G | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 3/11 | chr9 | 94434987 | ||||||
| chr9:94434998
|
C | A | 1 | a0001c0001t0001g0237 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.268-3403C>A | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 3/11 | chr9 | 94434998 | ||||||
| chr9:94435267
|
A | G | 1 | a0001c0001t0017g0022 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.268-3134A>G | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 3/11 | chr9 | 94435267 | ||||||
| chr9:94435427
|
C | T | 19 | a0001c0001t0002g0318a0001c0001t0002g0319a0001c0001t0002g0321others(16): Show | 19 | HG00639.hp1 HG01109.hp2 HG01256.hp2 others(16): Show |
intron_variant | MODIFIER | c.268-2974C>T | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 3/11 | chr9 | 94435427 | ||||||
| chr9:94435510
|
A | G | 1 | a0001c0001t0005g0002 | 2 | HG01069.hp1 HG01071.hp1 |
intron_variant | MODIFIER | c.268-2891A>G | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 3/11 | chr9 | 94435510 | ||||||
| chr9:94435643
|
CCTT | C | 55 | a0001c0001t0001g0001a0001c0001t0001g0086a0001c0001t0001g0225others(52): Show | 58 | HG00323.hp2 HG00673.hp1 HG00733.hp1 others(55): Show |
intron_variant | MODIFIER | c.268-2751_268-2749d others(5): Show |
MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr9 | 94435643 | |||||
| chr9:94435647
|
CTTCTTTT others(2): Show |
C | 8 | a0001c0001t0001g0242a0001c0001t0001g0250a0001c0001t0001g0251others(5): Show | 8 | HG00423.hp1 HG00423.hp2 NA18953.hp2 others(5): Show |
intron_variant | MODIFIER | c.268-2751_268-2743d others(11): Show |
MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr9 | 94435647 | |||||
| chr9:94435648
|
TTC | T | 109 | a0001c0001t0001g0003a0001c0001t0001g0081a0001c0001t0001g0082others(106): Show | 110 | HG00099.hp2 HG00280.hp2 HG00408.hp2 others(107): Show |
intron_variant | MODIFIER | c.268-2751_268-2750d others(4): Show |
MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr9 | 94435648 | |||||
| chr9:94435649
|
TC | T | 6 | a0001c0001t0001g0077a0001c0001t0001g0078a0001c0001t0001g0079others(3): Show | 6 | HG00323.hp1 HG01358.hp1 HG02559.hp2 others(3): Show |
intron_variant | MODIFIER | c.268-2751delC | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 3/11 | chr9 | 94435649 | ||||||
| chr9:94435650
|
C | CT | 22 | a0001c0001t0002g0130a0001c0001t0002g0137a0001c0001t0002g0148others(19): Show | 22 | HG00140.hp2 HG00639.hp1 HG00741.hp1 others(19): Show |
intron_variant | MODIFIER | c.268-2730dupT | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr9 | 94435650 | |||||
| chr9:94435650
|
C | CTT | 9 | a0001c0001t0006g0108a0001c0001t0006g0109a0001c0001t0006g0111others(6): Show | 9 | HG01243.hp2 HG02109.hp1 HG02280.hp2 others(6): Show |
intron_variant | MODIFIER | c.268-2731_268-2730d others(4): Show |
MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr9 | 94435650 | |||||
| chr9:94435650
|
C | T | 2 | a0001c0001t0013g0023a0001c0001t0013g0024 | 2 | HG02040.hp2 HG02132.hp2 |
intron_variant | MODIFIER | c.268-2751C>T | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 3/11 | chr9 | 94435650 | ||||||
| chr9:94435650
|
CT | C | 6 | a0001c0001t0002g0138a0001c0001t0002g0330a0001c0001t0007g0104others(3): Show | 6 | HG01256.hp2 HG01517.hp2 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.268-2730delT | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr9 | 94435650 | |||||
| chr9:94435740
|
C | T | 5 | a0001c0001t0008g0013a0001c0001t0008g0014a0001c0001t0008g0015others(2): Show | 5 | HG01081.hp1 HG02280.hp1 HG02559.hp1 others(2): Show |
intron_variant | MODIFIER | c.268-2661C>T | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 3/11 | chr9 | 94435740 | ||||||
| chr9:94435741
|
G | A | 1 | a0001c0001t0004g0043 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.268-2660G>A | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 3/11 | chr9 | 94435741 | ||||||
| chr9:94435779
|
C | T | 1 | a0001c0001t0017g0022 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.268-2622C>T | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 3/11 | chr9 | 94435779 | ||||||
| chr9:94435933
|
G | C | 1 | a0001c0001t0008g0017 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.268-2468G>C | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 3/11 | chr9 | 94435933 | ||||||
| chr9:94435970
|
GCTTT | G | 179 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0077others(176): Show | 183 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(180): Show |
intron_variant | MODIFIER | c.268-2426_268-2423d others(6): Show |
MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr9 | 94435970 | |||||
| chr9:94436102
|
T | A | 179 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0077others(176): Show | 183 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(180): Show |
intron_variant | MODIFIER | c.268-2299T>A | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 3/11 | chr9 | 94436102 | ||||||
| chr9:94436510
|
T | G | 53 | a0001c0001t0004g0027a0001c0001t0004g0028a0001c0001t0004g0035others(50): Show | 54 | HG00597.hp1 HG00639.hp2 HG00642.hp1 others(51): Show |
intron_variant | MODIFIER | c.268-1891T>G | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 3/11 | chr9 | 94436510 | ||||||
| chr9:94436533
|
T | G | 2 | a0001c0001t0001g0003a0001c0001t0001g0086 | 3 | HG00642.hp2 HG01257.hp2 HG01258.hp2 |
intron_variant | MODIFIER | c.268-1868T>G | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 3/11 | chr9 | 94436533 | ||||||
| chr9:94436691
|
C | A | 1 | a0001c0001t0003g0169 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.268-1710C>A | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 3/11 | chr9 | 94436691 | ||||||
| chr9:94436831
|
T | A | 1 | a0001c0001t0002g0123 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.268-1570T>A | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 3/11 | chr9 | 94436831 | ||||||
| chr9:94436890
|
A | G | 1 | a0001c0001t0003g0168 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.268-1511A>G | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 3/11 | chr9 | 94436890 | ||||||
| chr9:94437265
|
C | G | 53 | a0001c0001t0004g0027a0001c0001t0004g0028a0001c0001t0004g0035others(50): Show | 54 | HG00597.hp1 HG00639.hp2 HG00642.hp1 others(51): Show |
intron_variant | MODIFIER | c.268-1136C>G | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 3/11 | chr9 | 94437265 | ||||||
| chr9:94437357
|
C | T | 89 | a0001c0001t0001g0001a0001c0001t0001g0225a0001c0001t0001g0226others(86): Show | 91 | HG00323.hp2 HG00408.hp2 HG00423.hp1 others(88): Show |
intron_variant | MODIFIER | c.268-1044C>T | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 3/11 | chr9 | 94437357 | ||||||
| chr9:94437364
|
G | A | 1 | a0001c0001t0004g0070 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.268-1037G>A | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 3/11 | chr9 | 94437364 | ||||||
| chr9:94437370
|
C | T | 60 | a0001c0001t0002g0315a0001c0001t0002g0316a0001c0001t0002g0317others(57): Show | 60 | HG00140.hp2 HG00544.hp1 HG00639.hp1 others(57): Show |
intron_variant | MODIFIER | c.268-1031C>T | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 3/11 | chr9 | 94437370 | ||||||
| chr9:94437464
|
T | C | 1 | a0001c0001t0001g0310 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.268-937T>C | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 3/11 | chr9 | 94437464 | ||||||
| chr9:94437571
|
C | T | 1 | a0001c0001t0002g0316 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.268-830C>T | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 3/11 | chr9 | 94437571 | ||||||
| chr9:94437803
|
G | A | 7 | a0001c0001t0005g0002a0001c0001t0005g0030a0001c0001t0005g0031others(4): Show | 8 | HG01069.hp1 HG01071.hp1 HG02615.hp2 others(5): Show |
intron_variant | MODIFIER | c.268-598G>A | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 3/11 | chr9 | 94437803 | ||||||
| chr9:94437817
|
T | C | 1 | a0001c0001t0002g0139 | 1 | NA19054.hp1 | intron_variant | MODIFIER | c.268-584T>C | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 3/11 | chr9 | 94437817 | ||||||
| chr9:94437928
|
T | C | 1 | a0001c0001t0016g0025 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.268-473T>C | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 3/11 | chr9 | 94437928 | ||||||
| chr9:94438132
|
T | A | 2 | a0001c0001t0013g0023a0001c0001t0013g0024 | 2 | HG02040.hp2 HG02132.hp2 |
intron_variant | MODIFIER | c.268-269T>A | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 3/11 | chr9 | 94438132 | ||||||
| chr9:94438135
|
A | G | 1 | a0001c0001t0008g0016 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.268-266A>G | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 3/11 | chr9 | 94438135 | ||||||
| chr9:94438216
|
G | T | 1 | a0001c0001t0003g0204 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.268-185G>T | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 3/11 | chr9 | 94438216 | ||||||
| chr9:94438908
|
C | T | 1 | a0001c0001t0017g0022 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.395+380C>T | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 4/11 | chr9 | 94438908 | ||||||
| chr9:94438909
|
G | T | 1 | a0001c0001t0017g0022 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.395+381G>T | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 4/11 | chr9 | 94438909 | ||||||
| chr9:94438916
|
G | T | 1 | a0001c0001t0017g0022 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.395+388G>T | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 4/11 | chr9 | 94438916 | ||||||
| chr9:94438947
|
T | C | 19 | a0001c0001t0002g0318a0001c0001t0002g0319a0001c0001t0002g0321others(16): Show | 19 | HG00639.hp1 HG01109.hp2 HG01256.hp2 others(16): Show |
intron_variant | MODIFIER | c.395+419T>C | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 4/11 | chr9 | 94438947 | ||||||
| chr9:94438952
|
G | A | 1 | a0001c0001t0001g0243 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.395+424G>A | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 4/11 | chr9 | 94438952 | ||||||
| chr9:94438977
|
A | G | 4 | a0001c0001t0001g0077a0001c0001t0001g0078a0001c0001t0001g0079others(1): Show | 4 | HG00323.hp1 HG01358.hp1 HG02559.hp2 others(1): Show |
intron_variant | MODIFIER | c.395+449A>G | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 4/11 | chr9 | 94438977 | ||||||
| chr9:94439022
|
G | GT | 20 | a0001c0001t0002g0029a0001c0001t0002g0036a0001c0001t0002g0128others(17): Show | 20 | HG00099.hp1 HG00597.hp2 HG01243.hp1 others(17): Show |
intron_variant | MODIFIER | c.395+510dupT | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr9 | 94439022 | |||||
| chr9:94439022
|
G | GTTTTTT | 54 | a0001c0001t0001g0001a0001c0001t0001g0225a0001c0001t0001g0226others(51): Show | 56 | HG00408.hp2 HG00423.hp1 HG00423.hp2 others(53): Show |
intron_variant | MODIFIER | c.395+505_395+510dup others(6): Show |
MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr9 | 94439022 | |||||
| chr9:94439022
|
G | GTTTTTTT | 52 | a0001c0001t0001g0085a0001c0001t0001g0089a0001c0001t0001g0092others(49): Show | 53 | HG00099.hp2 HG00323.hp2 HG00438.hp1 others(50): Show |
intron_variant | MODIFIER | c.395+504_395+510dup others(7): Show |
MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr9 | 94439022 | |||||
| chr9:94439022
|
G | GTTTTTTT others(1): Show |
39 | a0001c0001t0001g0003a0001c0001t0001g0081a0001c0001t0001g0082others(36): Show | 40 | HG00280.hp2 HG00642.hp1 HG00642.hp2 others(37): Show |
intron_variant | MODIFIER | c.395+503_395+510dup others(8): Show |
MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr9 | 94439022 | |||||
| chr9:94439022
|
G | GTTTTTTT others(2): Show |
26 | a0001c0001t0001g0077a0001c0001t0001g0079a0001c0001t0004g0028others(23): Show | 26 | HG00323.hp1 HG00597.hp1 HG00639.hp2 others(23): Show |
intron_variant | MODIFIER | c.395+502_395+510dup others(9): Show |
MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr9 | 94439022 | |||||
| chr9:94439022
|
G | GTTTTTTT others(3): Show |
3 | a0001c0001t0001g0078a0001c0001t0001g0080a0001c0001t0004g0061 | 3 | HG01358.hp1 HG02559.hp2 NA18990.hp2 |
intron_variant | MODIFIER | c.395+501_395+510dup others(10): Show |
MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr9 | 94439022 | |||||
| chr9:94439068
|
CTGGA | C | 125 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0077others(122): Show | 128 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(125): Show |
intron_variant | MODIFIER | c.395+541_395+544del others(4): Show |
MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 4/11 | chr9 | 94439068 | ||||||
| chr9:94439166
|
C | T | 2 | a0001c0001t0001g0257a0001c0001t0001g0270 | 2 | NA18955.hp1 NA18983.hp1 |
intron_variant | MODIFIER | c.395+638C>T | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 4/11 | chr9 | 94439166 | ||||||
| chr9:94439268
|
A | G | 89 | a0001c0001t0001g0001a0001c0001t0001g0225a0001c0001t0001g0226others(86): Show | 91 | HG00323.hp2 HG00408.hp2 HG00423.hp1 others(88): Show |
intron_variant | MODIFIER | c.395+740A>G | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 4/11 | chr9 | 94439268 | ||||||
| chr9:94439272
|
GCTGGGAT others(19): Show |
G | 1 | a0001c0001t0016g0025 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.395+745_395+770del others(26): Show |
MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 4/11 | chr9 | 94439272 | ||||||
| chr9:94439309
|
A | AT | 26 | a0001c0001t0001g0003a0001c0001t0001g0077a0001c0001t0001g0078others(23): Show | 27 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(24): Show |
intron_variant | MODIFIER | c.395+796dupT | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr9 | 94439309 | |||||
| chr9:94439309
|
AT | A | 101 | a0001c0001t0001g0001a0001c0001t0001g0225a0001c0001t0001g0226others(98): Show | 103 | HG00323.hp2 HG00408.hp2 HG00423.hp1 others(100): Show |
intron_variant | MODIFIER | c.395+796delT | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr9 | 94439309 | |||||
| chr9:94439309
|
ATT | A | 52 | a0001c0001t0001g0307a0001c0001t0004g0027a0001c0001t0004g0028others(49): Show | 53 | HG00597.hp1 HG00639.hp2 HG00642.hp1 others(50): Show |
intron_variant | MODIFIER | c.395+795_395+796del others(2): Show |
MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr9 | 94439309 | |||||
| chr9:94439321
|
T | TC | 10 | a0001c0001t0008g0009a0001c0001t0008g0010a0001c0001t0008g0011others(7): Show | 10 | HG01081.hp1 HG02280.hp1 HG02559.hp1 others(7): Show |
intron_variant | MODIFIER | c.395+793_395+794ins others(1): Show |
MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 4/11 | chr9 | 94439321 | ||||||
| chr9:94439438
|
A | T | 1 | a0001c0001t0001g0084 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.395+910A>T | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 4/11 | chr9 | 94439438 | ||||||
| chr9:94439542
|
A | AT | 172 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0081others(169): Show | 176 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(173): Show |
intron_variant | MODIFIER | c.395+1029dupT | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr9 | 94439542 | |||||
| chr9:94439542
|
A | ATT | 6 | a0001c0001t0001g0077a0001c0001t0001g0078a0001c0001t0001g0079others(3): Show | 6 | HG00323.hp1 HG01358.hp1 HG02055.hp1 others(3): Show |
intron_variant | MODIFIER | c.395+1028_395+1029d others(4): Show |
MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr9 | 94439542 | |||||
| chr9:94439757
|
A | G | 1 | a0001c0001t0002g0118 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.396-1228A>G | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 4/11 | chr9 | 94439757 | ||||||
| chr9:94439918
|
C | T | 8 | a0001c0002t0009g0209a0001c0002t0009g0210a0001c0002t0009g0211others(5): Show | 8 | HG00140.hp2 HG00741.hp2 HG01255.hp2 others(5): Show |
intron_variant | MODIFIER | c.396-1067C>T | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 4/11 | chr9 | 94439918 | ||||||
| chr9:94440119
|
T | C | 2 | a0001c0001t0003g0206a0001c0001t0003g0207 | 2 | NA18968.hp1 NA19083.hp2 |
intron_variant | MODIFIER | c.396-866T>C | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 4/11 | chr9 | 94440119 | ||||||
| chr9:94440176
|
C | T | 5 | a0001c0001t0008g0013a0001c0001t0008g0014a0001c0001t0008g0015others(2): Show | 5 | HG01081.hp1 HG02280.hp1 HG02559.hp1 others(2): Show |
intron_variant | MODIFIER | c.396-809C>T | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 4/11 | chr9 | 94440176 | ||||||
| chr9:94440214
|
C | T | 3 | a0001c0001t0002g0218a0001c0001t0002g0219a0001c0001t0002g0220 | 3 | HG02818.hp1 HG03209.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.396-771C>T | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 4/11 | chr9 | 94440214 | ||||||
| chr9:94440299
|
G | A | 1 | a0001c0001t0005g0034 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.396-686G>A | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 4/11 | chr9 | 94440299 | ||||||
| chr9:94440303
|
A | G | 246 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0077others(243): Show | 250 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(247): Show |
intron_variant | MODIFIER | c.396-682A>G | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 4/11 | chr9 | 94440303 | ||||||
| chr9:94441243
|
G | T | 1 | a0001c0001t0017g0022 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.510+144G>T | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 5/11 | chr9 | 94441243 | ||||||
| chr9:94441347
|
A | G | 179 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0077others(176): Show | 183 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(180): Show |
intron_variant | MODIFIER | c.510+248A>G | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 5/11 | chr9 | 94441347 | ||||||
| chr9:94441381
|
A | G | 11 | a0001c0001t0006g0107a0001c0001t0006g0108a0001c0001t0006g0109others(8): Show | 11 | HG01243.hp2 HG02109.hp1 HG02280.hp2 others(8): Show |
intron_variant | MODIFIER | c.510+282A>G | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 5/11 | chr9 | 94441381 | ||||||
| chr9:94441384
|
A | G | 1 | a0001c0001t0008g0344 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.510+285A>G | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 5/11 | chr9 | 94441384 | ||||||
| chr9:94441506
|
A | G | 53 | a0001c0001t0004g0027a0001c0001t0004g0028a0001c0001t0004g0035others(50): Show | 54 | HG00597.hp1 HG00639.hp2 HG00642.hp1 others(51): Show |
intron_variant | MODIFIER | c.510+407A>G | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 5/11 | chr9 | 94441506 | ||||||
| chr9:94441611
|
G | T | 1 | a0001c0001t0001g0298 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.510+512G>T | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 5/11 | chr9 | 94441611 | ||||||
| chr9:94441721
|
G | C | 1 | a0001c0001t0002g0320 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.510+622G>C | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 5/11 | chr9 | 94441721 | ||||||
| chr9:94441728
|
AT | A | 11 | a0001c0001t0006g0107a0001c0001t0006g0108a0001c0001t0006g0109others(8): Show | 11 | HG01243.hp2 HG02109.hp1 HG02280.hp2 others(8): Show |
intron_variant | MODIFIER | c.510+632delT | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr9 | 94441728 | |||||
| chr9:94441758
|
C | T | 5 | a0001c0001t0008g0013a0001c0001t0008g0014a0001c0001t0008g0015others(2): Show | 5 | HG01081.hp1 HG02280.hp1 HG02559.hp1 others(2): Show |
intron_variant | MODIFIER | c.510+659C>T | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 5/11 | chr9 | 94441758 | ||||||
| chr9:94441807
|
G | T | 2 | a0001c0001t0004g0051a0001c0001t0004g0052 | 2 | HG03490.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.510+708G>T | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 5/11 | chr9 | 94441807 | ||||||
| chr9:94441848
|
G | A | 246 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0077others(243): Show | 250 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(247): Show |
intron_variant | MODIFIER | c.510+749G>A | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 5/11 | chr9 | 94441848 | ||||||
| chr9:94442321
|
A | C | 179 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0077others(176): Show | 183 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(180): Show |
intron_variant | MODIFIER | c.510+1222A>C | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 5/11 | chr9 | 94442321 | ||||||
| chr9:94442322
|
C | T | 179 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0077others(176): Show | 183 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(180): Show |
intron_variant | MODIFIER | c.510+1223C>T | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 5/11 | chr9 | 94442322 | ||||||
| chr9:94442396
|
C | T | 2 | a0001c0001t0013g0023a0001c0001t0013g0024 | 2 | HG02040.hp2 HG02132.hp2 |
intron_variant | MODIFIER | c.510+1297C>T | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 5/11 | chr9 | 94442396 | ||||||
| chr9:94442525
|
A | C | 18 | a0001c0001t0001g0003a0001c0001t0001g0081a0001c0001t0001g0082others(15): Show | 19 | HG00099.hp2 HG00280.hp2 HG00642.hp2 others(16): Show |
intron_variant | MODIFIER | c.510+1426A>C | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 5/11 | chr9 | 94442525 | ||||||
| chr9:94442578
|
C | T | 1 | a0001c0001t0017g0022 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.510+1479C>T | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 5/11 | chr9 | 94442578 | ||||||
| chr9:94442588
|
C | T | 11 | a0001c0001t0006g0107a0001c0001t0006g0108a0001c0001t0006g0109others(8): Show | 11 | HG01243.hp2 HG02109.hp1 HG02280.hp2 others(8): Show |
intron_variant | MODIFIER | c.510+1489C>T | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 5/11 | chr9 | 94442588 | ||||||
| chr9:94442619
|
G | A | 11 | a0001c0001t0006g0107a0001c0001t0006g0108a0001c0001t0006g0109others(8): Show | 11 | HG01243.hp2 HG02109.hp1 HG02280.hp2 others(8): Show |
intron_variant | MODIFIER | c.510+1520G>A | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 5/11 | chr9 | 94442619 | ||||||
| chr9:94442657
|
C | T | 1 | a0001c0001t0003g0161 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.510+1558C>T | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 5/11 | chr9 | 94442657 | ||||||
| chr9:94442679
|
C | T | 125 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0077others(122): Show | 128 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(125): Show |
intron_variant | MODIFIER | c.510+1580C>T | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 5/11 | chr9 | 94442679 | ||||||
| chr9:94442688
|
T | TA | 179 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0077others(176): Show | 183 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(180): Show |
intron_variant | MODIFIER | c.510+1593dupA | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr9 | 94442688 | |||||
| chr9:94442723
|
G | A | 9 | a0001c0001t0002g0153a0001c0001t0003g0120a0001c0001t0003g0125others(6): Show | 9 | HG00544.hp2 NA18747.hp1 NA18953.hp1 others(6): Show |
intron_variant | MODIFIER | c.510+1624G>A | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 5/11 | chr9 | 94442723 | ||||||
| chr9:94442830
|
C | T | 19 | a0001c0001t0002g0318a0001c0001t0002g0319a0001c0001t0002g0321others(16): Show | 19 | HG00639.hp1 HG01109.hp2 HG01256.hp2 others(16): Show |
intron_variant | MODIFIER | c.510+1731C>T | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 5/11 | chr9 | 94442830 | ||||||
| chr9:94442856
|
A | C | 2 | a0001c0001t0001g0289a0001c0001t0001g0290 | 2 | HG02074.hp2 HG02083.hp1 |
intron_variant | MODIFIER | c.510+1757A>C | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 5/11 | chr9 | 94442856 | ||||||
| chr9:94442938
|
G | C | 24 | a0001c0001t0004g0027a0001c0001t0004g0028a0001c0001t0004g0045others(21): Show | 24 | HG00597.hp1 HG00639.hp2 HG01934.hp1 others(21): Show |
intron_variant | MODIFIER | c.510+1839G>C | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 5/11 | chr9 | 94442938 | ||||||
| chr9:94443138
|
C | G | 1 | a0001c0001t0018g0041 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.511-1826C>G | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 5/11 | chr9 | 94443138 | ||||||
| chr9:94443264
|
C | T | 53 | a0001c0001t0004g0027a0001c0001t0004g0028a0001c0001t0004g0035others(50): Show | 54 | HG00597.hp1 HG00639.hp2 HG00642.hp1 others(51): Show |
intron_variant | MODIFIER | c.511-1700C>T | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 5/11 | chr9 | 94443264 | ||||||
| chr9:94443504
|
C | T | 1 | a0001c0001t0001g0233 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.511-1460C>T | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 5/11 | chr9 | 94443504 | ||||||
| chr9:94443538
|
CACTT | C | 125 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0077others(122): Show | 128 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(125): Show |
intron_variant | MODIFIER | c.511-1422_511-1419d others(6): Show |
MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr9 | 94443538 | |||||
| chr9:94443851
|
C | T | 4 | a0001c0001t0005g0018a0001c0001t0005g0019a0001c0001t0005g0020others(1): Show | 4 | HG01081.hp2 HG01109.hp1 HG02486.hp2 others(1): Show |
intron_variant | MODIFIER | c.511-1113C>T | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 5/11 | chr9 | 94443851 | ||||||
| chr9:94444132
|
T | C | 1 | a0001c0001t0001g0094 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.511-832T>C | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 5/11 | chr9 | 94444132 | ||||||
| chr9:94444146
|
A | G | 1 | a0001c0001t0005g0075 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.511-818A>G | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 5/11 | chr9 | 94444146 | ||||||
| chr9:94444333
|
C | G | 4 | a0001c0001t0004g0035a0001c0001t0004g0037a0001c0001t0004g0038others(1): Show | 4 | HG02896.hp1 HG02970.hp1 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.511-631C>G | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 5/11 | chr9 | 94444333 | ||||||
| chr9:94444348
|
C | T | 1 | a0001c0001t0016g0025 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.511-616C>T | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 5/11 | chr9 | 94444348 | ||||||
| chr9:94444455
|
G | T | 125 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0077others(122): Show | 128 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(125): Show |
intron_variant | MODIFIER | c.511-509G>T | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 5/11 | chr9 | 94444455 | ||||||
| chr9:94444674
|
G | A | 8 | a0001c0002t0009g0209a0001c0002t0009g0210a0001c0002t0009g0211others(5): Show | 8 | HG00140.hp2 HG00741.hp2 HG01255.hp2 others(5): Show |
intron_variant | MODIFIER | c.511-290G>A | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 5/11 | chr9 | 94444674 | ||||||
| chr9:94444869
|
G | C | 86 | a0001c0001t0001g0001a0001c0001t0001g0225a0001c0001t0001g0226others(83): Show | 88 | HG00323.hp2 HG00408.hp2 HG00423.hp1 others(85): Show |
intron_variant | MODIFIER | c.511-95G>C | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 5/11 | chr9 | 94444869 | ||||||
| chr9:94445311
|
T | A | 1 | a0001c0001t0002g0137 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.729+129T>A | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 6/11 | chr9 | 94445311 | ||||||
| chr9:94445387
|
G | A | 125 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0077others(122): Show | 128 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(125): Show |
intron_variant | MODIFIER | c.729+205G>A | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 6/11 | chr9 | 94445387 | ||||||
| chr9:94445718
|
T | C | 1 | a0001c0001t0002g0323 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.729+536T>C | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 6/11 | chr9 | 94445718 | ||||||
| chr9:94445769
|
GAA | G | 5 | a0001c0001t0008g0009a0001c0001t0008g0010a0001c0001t0008g0011others(2): Show | 5 | HG02818.hp2 HG02922.hp2 HG02976.hp2 others(2): Show |
intron_variant | MODIFIER | c.729+595_729+596del others(2): Show |
MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr9 | 94445769 | |||||
| chr9:94445770
|
A | G | 3 | a0001c0001t0001g0077a0001c0001t0001g0078a0001c0001t0001g0079 | 3 | HG00323.hp1 HG02559.hp2 HG03942.hp2 |
intron_variant | MODIFIER | c.729+588A>G | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 6/11 | chr9 | 94445770 | ||||||
| chr9:94445868
|
A | T | 1 | a0001c0001t0016g0025 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.729+686A>T | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 6/11 | chr9 | 94445868 | ||||||
| chr9:94445943
|
A | G | 1 | a0001c0001t0017g0022 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.729+761A>G | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 6/11 | chr9 | 94445943 | ||||||
| chr9:94445949
|
A | G | 89 | a0001c0001t0001g0001a0001c0001t0001g0225a0001c0001t0001g0226others(86): Show | 91 | HG00323.hp2 HG00408.hp2 HG00423.hp1 others(88): Show |
intron_variant | MODIFIER | c.729+767A>G | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 6/11 | chr9 | 94445949 | ||||||
| chr9:94446035
|
T | C | 53 | a0001c0001t0004g0027a0001c0001t0004g0028a0001c0001t0004g0035others(50): Show | 54 | HG00597.hp1 HG00639.hp2 HG00642.hp1 others(51): Show |
intron_variant | MODIFIER | c.730-788T>C | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 6/11 | chr9 | 94446035 | ||||||
| chr9:94446111
|
G | C | 179 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0077others(176): Show | 183 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(180): Show |
intron_variant | MODIFIER | c.730-712G>C | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 6/11 | chr9 | 94446111 | ||||||
| chr9:94446273
|
C | T | 2 | a0001c0001t0001g0082a0001c0001t0001g0096 | 2 | HG00733.hp2 HG01074.hp1 |
intron_variant | MODIFIER | c.730-550C>T | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 6/11 | chr9 | 94446273 | ||||||
| chr9:94446312
|
A | T | 1 | a0001c0001t0002g0143 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.730-511A>T | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 6/11 | chr9 | 94446312 | ||||||
| chr9:94446345
|
C | G | 126 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0077others(123): Show | 129 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(126): Show |
intron_variant | MODIFIER | c.730-478C>G | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 6/11 | chr9 | 94446345 | ||||||
| chr9:94446417
|
C | A | 182 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0077others(179): Show | 186 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(183): Show |
intron_variant | MODIFIER | c.730-406C>A | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 6/11 | chr9 | 94446417 | ||||||
| chr9:94446422
|
C | T | 1 | a0001c0001t0004g0073 | 1 | NA19075.hp2 | intron_variant | MODIFIER | c.730-401C>T | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 6/11 | chr9 | 94446422 | ||||||
| chr9:94446428
|
C | T | 1 | a0001c0001t0017g0022 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.730-395C>T | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 6/11 | chr9 | 94446428 | ||||||
| chr9:94446641
|
T | C | 246 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0077others(243): Show | 250 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(247): Show |
intron_variant | MODIFIER | c.730-182T>C | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 6/11 | chr9 | 94446641 | ||||||
| chr9:94446678
|
A | G | 1 | a0001c0001t0002g0004 | 2 | HG02083.hp2 NA19080.hp2 |
intron_variant | MODIFIER | c.730-145A>G | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 6/11 | chr9 | 94446678 | ||||||
| chr9:94446701
|
A | G | 4 | a0001c0001t0003g0176a0001c0001t0003g0177a0001c0001t0003g0178others(1): Show | 4 | HG00140.hp1 HG01074.hp2 HG02602.hp2 others(1): Show |
intron_variant | MODIFIER | c.730-122A>G | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 6/11 | chr9 | 94446701 | ||||||
| chr9:94446784
|
T | C | 125 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0077others(122): Show | 128 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(125): Show |
intron_variant | MODIFIER | c.730-39T>C | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 6/11 | chr9 | 94446784 | ||||||
| chr9:94447085
|
A | C | 11 | a0001c0001t0006g0107a0001c0001t0006g0108a0001c0001t0006g0109others(8): Show | 11 | HG01243.hp2 HG02109.hp1 HG02280.hp2 others(8): Show |
intron_variant | MODIFIER | c.843+149A>C | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 7/11 | chr9 | 94447085 | ||||||
| chr9:94447171
|
A | T | 8 | a0001c0002t0009g0209a0001c0002t0009g0210a0001c0002t0009g0211others(5): Show | 8 | HG00140.hp2 HG00741.hp2 HG01255.hp2 others(5): Show |
intron_variant | MODIFIER | c.843+235A>T | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 7/11 | chr9 | 94447171 | ||||||
| chr9:94447183
|
C | CT | 40 | a0001c0001t0002g0029a0001c0001t0002g0036a0001c0001t0002g0039others(37): Show | 40 | HG00639.hp1 HG01109.hp2 HG01243.hp1 others(37): Show |
intron_variant | MODIFIER | c.843+260dupT | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr9 | 94447183 | |||||
| chr9:94447183
|
CT | C | 14 | a0001c0001t0001g0285a0001c0001t0001g0286a0001c0001t0003g0156others(11): Show | 14 | HG01081.hp1 HG02109.hp2 HG02258.hp2 others(11): Show |
intron_variant | MODIFIER | c.843+260delT | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr9 | 94447183 | |||||
| chr9:94447258
|
C | T | 2 | a0001c0001t0002g0331a0001c0001t0020g0332 | 2 | HG01255.hp1 HG02895.hp2 |
intron_variant | MODIFIER | c.843+322C>T | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 7/11 | chr9 | 94447258 | ||||||
| chr9:94447325
|
G | A | 1 | a0001c0001t0016g0025 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.843+389G>A | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 7/11 | chr9 | 94447325 | ||||||
| chr9:94447331
|
T | C | 246 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0077others(243): Show | 250 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(247): Show |
intron_variant | MODIFIER | c.843+395T>C | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 7/11 | chr9 | 94447331 | ||||||
| chr9:94447379
|
C | T | 6 | a0001c0001t0002g0119a0001c0001t0002g0123a0001c0001t0002g0138others(3): Show | 6 | NA18948.hp2 NA18957.hp2 NA18991.hp2 others(3): Show |
intron_variant | MODIFIER | c.843+443C>T | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 7/11 | chr9 | 94447379 | ||||||
| chr9:94447380
|
G | A | 3 | a0001c0001t0001g0229a0001c0001t0001g0310a0001c0001t0001g0311 | 3 | HG02258.hp1 HG02622.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.843+444G>A | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 7/11 | chr9 | 94447380 | ||||||
| chr9:94447392
|
T | C | 246 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0077others(243): Show | 250 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(247): Show |
intron_variant | MODIFIER | c.843+456T>C | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 7/11 | chr9 | 94447392 | ||||||
| chr9:94447438
|
C | G | 1 | a0001c0001t0017g0022 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.843+502C>G | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 7/11 | chr9 | 94447438 | ||||||
| chr9:94447479
|
CTG | C | 41 | a0001c0001t0001g0003a0001c0001t0001g0077a0001c0001t0001g0079others(38): Show | 42 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(39): Show |
intron_variant | MODIFIER | c.843+545_843+546del others(2): Show |
MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr9 | 94447479 | |||||
| chr9:94447480
|
TG | T | 3 | a0001c0001t0001g0078a0001c0001t0001g0080a0001c0001t0001g0090 | 3 | HG01358.hp1 HG02055.hp1 HG02559.hp2 |
intron_variant | MODIFIER | c.843+545delG | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 7/11 | chr9 | 94447480 | ||||||
| chr9:94447481
|
G | GT | 8 | a0001c0001t0002g0149a0001c0001t0002g0187a0001c0001t0002g0224others(5): Show | 8 | HG02055.hp2 HG02300.hp2 HG02738.hp1 others(5): Show |
intron_variant | MODIFIER | c.843+565dupT | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr9 | 94447481 | |||||
| chr9:94447481
|
GT | G | 14 | a0001c0001t0001g0285a0001c0001t0001g0286a0001c0001t0001g0307others(11): Show | 14 | HG01081.hp2 HG01109.hp1 HG01516.hp2 others(11): Show |
intron_variant | MODIFIER | c.843+565delT | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr9 | 94447481 | |||||
| chr9:94447481
|
GTT | G | 137 | a0001c0001t0001g0001a0001c0001t0001g0226a0001c0001t0001g0228others(134): Show | 139 | HG00140.hp2 HG00323.hp2 HG00408.hp2 others(136): Show |
intron_variant | MODIFIER | c.843+564_843+565del others(2): Show |
MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr9 | 94447481 | |||||
| chr9:94447605
|
T | C | 1 | a0001c0001t0003g0166 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.843+669T>C | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 7/11 | chr9 | 94447605 | ||||||
| chr9:94447626
|
G | A | 4 | a0001c0001t0001g0077a0001c0001t0001g0078a0001c0001t0001g0079others(1): Show | 4 | HG00323.hp1 HG01358.hp1 HG02559.hp2 others(1): Show |
intron_variant | MODIFIER | c.843+690G>A | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 7/11 | chr9 | 94447626 | ||||||
| chr9:94447694
|
T | A | 53 | a0001c0001t0004g0027a0001c0001t0004g0028a0001c0001t0004g0035others(50): Show | 54 | HG00597.hp1 HG00639.hp2 HG00642.hp1 others(51): Show |
intron_variant | MODIFIER | c.843+758T>A | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 7/11 | chr9 | 94447694 | ||||||
| chr9:94447753
|
C | T | 1 | a0001c0001t0016g0025 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.843+817C>T | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 7/11 | chr9 | 94447753 | ||||||
| chr9:94448107
|
T | TA | 179 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0077others(176): Show | 183 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(180): Show |
intron_variant | MODIFIER | c.843+1173dupA | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr9 | 94448107 | |||||
| chr9:94448242
|
G | A | 1 | a0001c0001t0004g0042 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.843+1306G>A | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 7/11 | chr9 | 94448242 | ||||||
| chr9:94448308
|
C | T | 1 | a0001c0001t0002g0331 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.843+1372C>T | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 7/11 | chr9 | 94448308 | ||||||
| chr9:94448363
|
AC | A | 36 | a0001c0001t0002g0029a0001c0001t0002g0036a0001c0001t0002g0039others(33): Show | 36 | HG00639.hp1 HG01109.hp2 HG01243.hp1 others(33): Show |
intron_variant | MODIFIER | c.843+1429delC | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr9 | 94448363 | |||||
| chr9:94448463
|
G | C | 1 | a0001c0001t0005g0018 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.843+1527G>C | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 7/11 | chr9 | 94448463 | ||||||
| chr9:94448605
|
T | C | 2 | a0001c0001t0013g0023a0001c0001t0013g0024 | 2 | HG02040.hp2 HG02132.hp2 |
intron_variant | MODIFIER | c.843+1669T>C | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 7/11 | chr9 | 94448605 | ||||||
| chr9:94448610
|
C | T | 53 | a0001c0001t0004g0027a0001c0001t0004g0028a0001c0001t0004g0035others(50): Show | 54 | HG00597.hp1 HG00639.hp2 HG00642.hp1 others(51): Show |
intron_variant | MODIFIER | c.843+1674C>T | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 7/11 | chr9 | 94448610 | ||||||
| chr9:94448715
|
C | T | 1 | a0001c0001t0002g0218 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.843+1779C>T | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 7/11 | chr9 | 94448715 | ||||||
| chr9:94448783
|
C | T | 1 | a0001c0001t0001g0284 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.843+1847C>T | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 7/11 | chr9 | 94448783 | ||||||
| chr9:94448789
|
C | T | 1 | a0002c0004t0001g0299 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.843+1853C>T | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 7/11 | chr9 | 94448789 | ||||||
| chr9:94449030
|
T | C | 3 | a0001c0002t0009g0210a0001c0002t0009g0214a0001c0002t0009g0215 | 3 | HG01255.hp2 HG01361.hp1 HG04204.hp2 |
intron_variant | MODIFIER | c.843+2094T>C | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 7/11 | chr9 | 94449030 | ||||||
| chr9:94449160
|
A | G | 1 | a0001c0001t0001g0269 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.843+2224A>G | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 7/11 | chr9 | 94449160 | ||||||
| chr9:94449374
|
A | G | 89 | a0001c0001t0001g0001a0001c0001t0001g0225a0001c0001t0001g0226others(86): Show | 91 | HG00323.hp2 HG00408.hp2 HG00423.hp1 others(88): Show |
intron_variant | MODIFIER | c.844-2082A>G | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 7/11 | chr9 | 94449374 | ||||||
| chr9:94449434
|
T | C | 3 | a0001c0001t0002g0218a0001c0001t0002g0219a0001c0001t0002g0220 | 3 | HG02818.hp1 HG03209.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.844-2022T>C | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 7/11 | chr9 | 94449434 | ||||||
| chr9:94449467
|
AG | A | 3 | a0001c0001t0001g0001a0001c0001t0001g0307a0001c0001t0001g0309 | 5 | NA18944.hp2 NA18950.hp1 NA18997.hp1 others(2): Show |
intron_variant | MODIFIER | c.844-1987delG | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr9 | 94449467 | |||||
| chr9:94449502
|
C | T | 246 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0077others(243): Show | 250 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(247): Show |
intron_variant | MODIFIER | c.844-1954C>T | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 7/11 | chr9 | 94449502 | ||||||
| chr9:94449612
|
A | G | 3 | a0001c0001t0002g0218a0001c0001t0002g0219a0001c0001t0002g0220 | 3 | HG02818.hp1 HG03209.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.844-1844A>G | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 7/11 | chr9 | 94449612 | ||||||
| chr9:94449734
|
A | G | 1 | a0001c0001t0016g0025 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.844-1722A>G | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 7/11 | chr9 | 94449734 | ||||||
| chr9:94449778
|
A | G | 2 | a0001c0001t0001g0310a0001c0001t0001g0311 | 2 | HG02258.hp1 HG02622.hp1 |
intron_variant | MODIFIER | c.844-1678A>G | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 7/11 | chr9 | 94449778 | ||||||
| chr9:94449914
|
A | C | 26 | a0001c0001t0001g0003a0001c0001t0001g0077a0001c0001t0001g0078others(23): Show | 27 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(24): Show |
intron_variant | MODIFIER | c.844-1542A>C | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 7/11 | chr9 | 94449914 | ||||||
| chr9:94449976
|
G | A | 246 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0077others(243): Show | 250 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(247): Show |
intron_variant | MODIFIER | c.844-1480G>A | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 7/11 | chr9 | 94449976 | ||||||
| chr9:94450042
|
G | A | 2 | a0001c0001t0007g0104a0001c0001t0007g0106 | 2 | HG02630.hp1 HG02895.hp1 |
intron_variant | MODIFIER | c.844-1414G>A | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 7/11 | chr9 | 94450042 | ||||||
| chr9:94450176
|
A | G | 3 | a0001c0001t0002g0340a0001c0001t0002g0341a0001c0001t0002g0342 | 3 | HG01884.hp2 HG02886.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.844-1280A>G | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 7/11 | chr9 | 94450176 | ||||||
| chr9:94450315
|
T | C | 1 | a0001c0001t0001g0288 | 1 | NA18943.hp2 | intron_variant | MODIFIER | c.844-1141T>C | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 7/11 | chr9 | 94450315 | ||||||
| chr9:94450341
|
G | A | 3 | a0001c0001t0001g0304a0001c0001t0001g0305a0001c0001t0001g0306 | 3 | HG02451.hp2 HG03471.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.844-1115G>A | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 7/11 | chr9 | 94450341 | ||||||
| chr9:94450437
|
T | C | 1 | a0001c0001t0007g0223 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.844-1019T>C | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 7/11 | chr9 | 94450437 | ||||||
| chr9:94450440
|
C | T | 11 | a0001c0001t0006g0107a0001c0001t0006g0108a0001c0001t0006g0109others(8): Show | 11 | HG01243.hp2 HG02109.hp1 HG02280.hp2 others(8): Show |
intron_variant | MODIFIER | c.844-1016C>T | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 7/11 | chr9 | 94450440 | ||||||
| chr9:94450492
|
A | AACTT | 9 | a0001c0001t0007g0099a0001c0001t0007g0100a0001c0001t0007g0101others(6): Show | 9 | HG00544.hp1 HG01884.hp1 HG02630.hp1 others(6): Show |
intron_variant | MODIFIER | c.844-964_844-963ins others(4): Show |
MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 7/11 | chr9 | 94450492 | ||||||
| chr9:94450493
|
C | CTTTTTTT others(3): Show |
11 | a0001c0001t0006g0107a0001c0001t0006g0108a0001c0001t0006g0109others(8): Show | 11 | HG01243.hp2 HG02109.hp1 HG02280.hp2 others(8): Show |
intron_variant | MODIFIER | c.844-958_844-949dup others(10): Show |
MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr9 | 94450493 | |||||
| chr9:94450493
|
C | CTTTTTTT others(5): Show |
23 | a0001c0001t0004g0045a0001c0001t0004g0059a0001c0001t0005g0002others(20): Show | 24 | HG00140.hp2 HG00741.hp2 HG01069.hp1 others(21): Show |
intron_variant | MODIFIER | c.844-960_844-949dup others(12): Show |
MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr9 | 94450493 | |||||
| chr9:94450493
|
C | CTTTTTTT others(6): Show |
34 | a0001c0001t0001g0225a0001c0001t0002g0218a0001c0001t0002g0219others(31): Show | 34 | HG00597.hp1 HG00642.hp1 HG00733.hp1 others(31): Show |
intron_variant | MODIFIER | c.844-961_844-949dup others(13): Show |
MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr9 | 94450493 | |||||
| chr9:94450493
|
C | CTTTTTTT others(7): Show |
72 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0081others(69): Show | 75 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(72): Show |
intron_variant | MODIFIER | c.844-962_844-949dup others(14): Show |
MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr9 | 94450493 | |||||
| chr9:94450493
|
C | CTTTTTTT others(8): Show |
43 | a0001c0001t0001g0078a0001c0001t0001g0080a0001c0001t0001g0086others(40): Show | 43 | HG00408.hp2 HG00423.hp1 HG00423.hp2 others(40): Show |
intron_variant | MODIFIER | c.844-949_844-948ins others(15): Show |
MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr9 | 94450493 | |||||
| chr9:94450493
|
C | CTTTTTTT others(9): Show |
13 | a0001c0001t0001g0079a0001c0001t0001g0230a0001c0001t0001g0243others(10): Show | 13 | HG01081.hp1 HG01106.hp2 HG02280.hp1 others(10): Show |
intron_variant | MODIFIER | c.844-949_844-948ins others(16): Show |
MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr9 | 94450493 | |||||
| chr9:94450493
|
C | CTTTTTTT others(10): Show |
2 | a0001c0001t0008g0010a0001c0001t0008g0011 | 2 | HG02818.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.844-949_844-948ins others(17): Show |
MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr9 | 94450493 | |||||
| chr9:94450493
|
C | CTTTTTTT others(15): Show |
1 | a0001c0001t0001g0077 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.844-949_844-948ins others(22): Show |
MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr9 | 94450493 | |||||
| chr9:94450493
|
C | T | 9 | a0001c0001t0007g0099a0001c0001t0007g0100a0001c0001t0007g0101others(6): Show | 9 | HG00544.hp1 HG01884.hp1 HG02630.hp1 others(6): Show |
intron_variant | MODIFIER | c.844-963C>T | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 7/11 | chr9 | 94450493 | ||||||
| chr9:94450507
|
T | TTTTTTTT others(6): Show |
1 | a0001c0001t0002g0328 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.844-949_844-948ins others(13): Show |
MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 7/11 | chr9 | 94450507 | ||||||
| chr9:94450507
|
T | TTTTTTTT others(7): Show |
1 | a0001c0001t0002g0319 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.844-949_844-948ins others(14): Show |
MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 7/11 | chr9 | 94450507 | ||||||
| chr9:94450507
|
T | TTTTTTTT others(11): Show |
1 | a0001c0001t0003g0007 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.844-949_844-948ins others(18): Show |
MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 7/11 | chr9 | 94450507 | ||||||
| chr9:94450507
|
T | TTTTTTTT others(12): Show |
2 | a0001c0001t0002g0331a0001c0001t0003g0008 | 2 | HG02895.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.844-949_844-948ins others(19): Show |
MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 7/11 | chr9 | 94450507 | ||||||
| chr9:94450507
|
T | TTTTTTTT others(13): Show |
5 | a0001c0001t0002g0315a0001c0001t0002g0317a0001c0001t0002g0320others(2): Show | 5 | HG01255.hp1 HG02630.hp2 HG02717.hp2 others(2): Show |
intron_variant | MODIFIER | c.844-949_844-948ins others(20): Show |
MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 7/11 | chr9 | 94450507 | ||||||
| chr9:94450507
|
T | TTTTTTTT others(14): Show |
6 | a0001c0001t0002g0029a0001c0001t0002g0036a0001c0001t0002g0330others(3): Show | 6 | HG01243.hp1 HG01256.hp2 HG01496.hp2 others(3): Show |
intron_variant | MODIFIER | c.844-949_844-948ins others(21): Show |
MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 7/11 | chr9 | 94450507 | ||||||
| chr9:94450507
|
T | TTTTTTTT others(15): Show |
6 | a0001c0001t0002g0323a0001c0001t0002g0324a0001c0001t0002g0334others(3): Show | 6 | HG01884.hp2 HG02451.hp1 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.844-949_844-948ins others(22): Show |
MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 7/11 | chr9 | 94450507 | ||||||
| chr9:94450507
|
T | TTTTTTTT others(16): Show |
7 | a0001c0001t0002g0039a0001c0001t0002g0040a0001c0001t0002g0316others(4): Show | 7 | HG00639.hp1 HG01516.hp1 HG01517.hp1 others(4): Show |
intron_variant | MODIFIER | c.844-949_844-948ins others(23): Show |
MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 7/11 | chr9 | 94450507 | ||||||
| chr9:94450507
|
T | TTTTTTTT others(17): Show |
3 | a0001c0001t0002g0318a0001c0001t0002g0321a0001c0001t0002g0335 | 3 | HG01109.hp2 NA18978.hp1 NA18979.hp1 |
intron_variant | MODIFIER | c.844-949_844-948ins others(24): Show |
MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 7/11 | chr9 | 94450507 | ||||||
| chr9:94450507
|
T | TTTTTTTT others(18): Show |
2 | a0001c0001t0002g0326a0001c0001t0002g0333 | 2 | NA19057.hp2 NA19070.hp1 |
intron_variant | MODIFIER | c.844-949_844-948ins others(25): Show |
MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 7/11 | chr9 | 94450507 | ||||||
| chr9:94450507
|
T | TTTTTTTT others(19): Show |
2 | a0001c0001t0002g0327a0001c0001t0002g0343 | 2 | HG02015.hp1 NA19087.hp1 |
intron_variant | MODIFIER | c.844-949_844-948ins others(26): Show |
MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 7/11 | chr9 | 94450507 | ||||||
| chr9:94450540
|
A | T | 179 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0077others(176): Show | 183 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(180): Show |
intron_variant | MODIFIER | c.844-916A>T | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 7/11 | chr9 | 94450540 | ||||||
| chr9:94450651
|
A | G | 235 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0077others(232): Show | 239 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(236): Show |
intron_variant | MODIFIER | c.844-805A>G | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 7/11 | chr9 | 94450651 | ||||||
| chr9:94450687
|
C | T | 1 | a0001c0001t0003g0135 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.844-769C>T | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 7/11 | chr9 | 94450687 | ||||||
| chr9:94450688
|
G | A | 179 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0077others(176): Show | 183 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(180): Show |
intron_variant | MODIFIER | c.844-768G>A | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 7/11 | chr9 | 94450688 | ||||||
| chr9:94450917
|
C | T | 3 | a0001c0001t0002g0218a0001c0001t0002g0219a0001c0001t0002g0220 | 3 | HG02818.hp1 HG03209.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.844-539C>T | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 7/11 | chr9 | 94450917 | ||||||
| chr9:94450986
|
G | A | 1 | a0001c0001t0017g0022 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.844-470G>A | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 7/11 | chr9 | 94450986 | ||||||
| chr9:94451162
|
A | G | 89 | a0001c0001t0001g0001a0001c0001t0001g0225a0001c0001t0001g0226others(86): Show | 91 | HG00323.hp2 HG00408.hp2 HG00423.hp1 others(88): Show |
intron_variant | MODIFIER | c.844-294A>G | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 7/11 | chr9 | 94451162 | ||||||
| chr9:94451201
|
A | G | 13 | a0001c0001t0002g0029a0001c0001t0002g0036a0001c0001t0002g0039others(10): Show | 13 | HG01243.hp1 HG01255.hp1 HG01516.hp1 others(10): Show |
intron_variant | MODIFIER | c.844-255A>G | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 7/11 | chr9 | 94451201 | ||||||
| chr9:94451223
|
A | G | 1 | a0001c0001t0004g0070 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.844-233A>G | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 7/11 | chr9 | 94451223 | ||||||
| chr9:94451265
|
G | C | 1 | a0001c0001t0001g0091 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.844-191G>C | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 7/11 | chr9 | 94451265 | ||||||
| chr9:94451278
|
G | A | 41 | a0001c0001t0004g0027a0001c0001t0004g0028a0001c0001t0004g0035others(38): Show | 41 | HG00597.hp1 HG00639.hp2 HG00642.hp1 others(38): Show |
intron_variant | MODIFIER | c.844-178G>A | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 7/11 | chr9 | 94451278 | ||||||
| chr9:94451436
|
TTTTCA | T | 10 | a0001c0001t0008g0009a0001c0001t0008g0010a0001c0001t0008g0011others(7): Show | 10 | HG01081.hp1 HG02280.hp1 HG02559.hp1 others(7): Show |
splice_region_variant&intron_variant | LOW | c.844-10_844-6delATT others(2): Show |
MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr9 | 94451436 | |||||
| chr9:94451561
|
A | T | 19 | a0001c0001t0001g0003a0001c0001t0001g0081a0001c0001t0001g0082others(16): Show | 20 | HG00099.hp2 HG00280.hp2 HG00642.hp2 others(17): Show |
intron_variant | MODIFIER | c.915+34A>T | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 8/11 | chr9 | 94451561 | ||||||
| chr9:94451652
|
C | G | 1 | a0001c0001t0018g0041 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.915+125C>G | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 8/11 | chr9 | 94451652 | ||||||
| chr9:94451936
|
G | A | 8 | a0001c0002t0009g0209a0001c0002t0009g0210a0001c0002t0009g0211others(5): Show | 8 | HG00140.hp2 HG00741.hp2 HG01255.hp2 others(5): Show |
intron_variant | MODIFIER | c.915+409G>A | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 8/11 | chr9 | 94451936 | ||||||
| chr9:94452324
|
C | T | 1 | a0001c0001t0016g0025 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.915+797C>T | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 8/11 | chr9 | 94452324 | ||||||
| chr9:94452468
|
G | A | 1 | a0001c0001t0002g0315 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.915+941G>A | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 8/11 | chr9 | 94452468 | ||||||
| chr9:94452594
|
C | A | 36 | a0001c0001t0002g0029a0001c0001t0002g0036a0001c0001t0002g0039others(33): Show | 36 | HG00639.hp1 HG01109.hp2 HG01243.hp1 others(33): Show |
intron_variant | MODIFIER | c.915+1067C>A | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 8/11 | chr9 | 94452594 | ||||||
| chr9:94452614
|
A | AAT | 50 | a0001c0001t0002g0128a0001c0001t0002g0218a0001c0001t0002g0220others(47): Show | 50 | HG00099.hp1 HG00597.hp1 HG00639.hp2 others(47): Show |
intron_variant | MODIFIER | c.915+1104_915+1105d others(4): Show |
MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr9 | 94452614 | |||||
| chr9:94452614
|
AAT | A | 19 | a0001c0001t0001g0003a0001c0001t0001g0081a0001c0001t0001g0082others(16): Show | 20 | HG00099.hp2 HG00280.hp2 HG00642.hp2 others(17): Show |
intron_variant | MODIFIER | c.915+1104_915+1105d others(4): Show |
MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr9 | 94452614 | |||||
| chr9:94452630
|
TATTTTCA others(21): Show |
T | 1 | a0001c0001t0002g0219 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.915+1106_915+1133d others(30): Show |
MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr9 | 94452630 | |||||
| chr9:94452632
|
T | C | 1 | a0001c0001t0003g0127 | 1 | HG02273.hp2 | intron_variant | MODIFIER | c.915+1105T>C | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 8/11 | chr9 | 94452632 | ||||||
| chr9:94452635
|
TCATATAT others(23): Show |
T | 6 | a0001c0001t0004g0038a0001c0001t0005g0002a0001c0001t0005g0030others(3): Show | 7 | HG01069.hp1 HG01071.hp1 HG02809.hp2 others(4): Show |
intron_variant | MODIFIER | c.915+1109_915+1138d others(32): Show |
MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 8/11 | chr9 | 94452635 | ||||||
| chr9:94452638
|
TATATATA others(3): Show |
T | 6 | a0001c0001t0002g0118a0001c0001t0003g0173a0001c0001t0003g0174others(3): Show | 6 | HG01346.hp1 HG04228.hp1 NA18955.hp2 others(3): Show |
intron_variant | MODIFIER | c.915+1148_915+1157d others(12): Show |
MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr9 | 94452638 | |||||
| chr9:94452638
|
TATATATA others(41): Show |
T | 7 | a0001c0001t0004g0045a0001c0001t0004g0046a0001c0001t0004g0047others(4): Show | 7 | NA18995.hp2 NA19000.hp2 NA19001.hp2 others(4): Show |
intron_variant | MODIFIER | c.915+1128_915+1175d others(50): Show |
MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr9 | 94452638 | |||||
| chr9:94452640
|
TATATATT others(31): Show |
T | 90 | a0001c0001t0001g0260a0001c0001t0001g0261a0001c0001t0002g0029others(87): Show | 90 | HG00597.hp1 HG00639.hp1 HG00639.hp2 others(87): Show |
intron_variant | MODIFIER | c.915+1138_915+1175d others(40): Show |
MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr9 | 94452640 | |||||
| chr9:94452650
|
TATATATT others(21): Show |
T | 136 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0081others(133): Show | 139 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(136): Show |
intron_variant | MODIFIER | c.915+1148_915+1175d others(30): Show |
MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr9 | 94452650 | |||||
| chr9:94452650
|
TATATATT others(39): Show |
T | 1 | a0001c0001t0004g0057 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.915+1150_915+1195d others(48): Show |
MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr9 | 94452650 | |||||
| chr9:94452658
|
CAT | C | 4 | a0001c0001t0001g0077a0001c0001t0001g0078a0001c0001t0001g0079others(1): Show | 4 | HG00323.hp1 HG01358.hp1 HG02559.hp2 others(1): Show |
intron_variant | MODIFIER | c.915+1138_915+1139d others(4): Show |
MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr9 | 94452658 | |||||
| chr9:94452658
|
CATATATA others(41): Show |
C | 1 | a0001c0001t0004g0044 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.915+1138_915+1185d others(50): Show |
MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr9 | 94452658 | |||||
| chr9:94452660
|
T | TATATATT others(11): Show |
1 | a0001c0001t0003g0157 | 1 | HG01169.hp2 | intron_variant | MODIFIER | c.915+1176_915+1193d others(20): Show |
MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr9 | 94452660 | |||||
| chr9:94452660
|
TATATATT others(11): Show |
T | 1 | a0001c0001t0001g0290 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.915+1176_915+1193d others(20): Show |
MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr9 | 94452660 | |||||
| chr9:94452665
|
A | T | 1 | a0001c0001t0002g0219 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.915+1138A>T | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 8/11 | chr9 | 94452665 | ||||||
| chr9:94452672
|
TATATTC | T | 7 | a0001c0001t0002g0219a0001c0001t0004g0038a0001c0001t0005g0002others(4): Show | 8 | HG01069.hp1 HG01071.hp1 HG02809.hp2 others(5): Show |
intron_variant | MODIFIER | c.915+1150_915+1155d others(8): Show |
MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr9 | 94452672 | |||||
| chr9:94452679
|
ATATATTC others(61): Show |
A | 4 | a0001c0001t0001g0077a0001c0001t0001g0078a0001c0001t0001g0079others(1): Show | 4 | HG00323.hp1 HG01358.hp1 HG02559.hp2 others(1): Show |
intron_variant | MODIFIER | c.915+1156_916-1208d others(70): Show |
MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr9 | 94452679 | |||||
| chr9:94452715
|
ATATATAT others(25): Show |
A | 19 | a0001c0001t0001g0003a0001c0001t0001g0081a0001c0001t0001g0082others(16): Show | 20 | HG00099.hp2 HG00280.hp2 HG00642.hp2 others(17): Show |
intron_variant | MODIFIER | c.915+1192_916-1208d others(34): Show |
MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr9 | 94452715 | |||||
| chr9:94452758
|
A | C | 23 | a0001c0001t0001g0003a0001c0001t0001g0077a0001c0001t0001g0078others(20): Show | 24 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(21): Show |
intron_variant | MODIFIER | c.916-1200A>C | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 8/11 | chr9 | 94452758 | ||||||
| chr9:94453042
|
C | T | 53 | a0001c0001t0004g0027a0001c0001t0004g0028a0001c0001t0004g0035others(50): Show | 54 | HG00597.hp1 HG00639.hp2 HG00642.hp1 others(51): Show |
intron_variant | MODIFIER | c.916-916C>T | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 8/11 | chr9 | 94453042 | ||||||
| chr9:94453052
|
T | A | 8 | a0001c0002t0009g0209a0001c0002t0009g0210a0001c0002t0009g0211others(5): Show | 8 | HG00140.hp2 HG00741.hp2 HG01255.hp2 others(5): Show |
intron_variant | MODIFIER | c.916-906T>A | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 8/11 | chr9 | 94453052 | ||||||
| chr9:94453094
|
C | A | 1 | a0001c0001t0002g0137 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.916-864C>A | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 8/11 | chr9 | 94453094 | ||||||
| chr9:94453109
|
A | G | 2 | a0001c0001t0002g0321a0001c0001t0002g0322 | 2 | HG00639.hp1 HG01109.hp2 |
intron_variant | MODIFIER | c.916-849A>G | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 8/11 | chr9 | 94453109 | ||||||
| chr9:94453139
|
C | G | 1 | a0001c0001t0002g0324 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.916-819C>G | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 8/11 | chr9 | 94453139 | ||||||
| chr9:94453148
|
C | CT | 8 | a0001c0001t0002g0141a0001c0001t0002g0151a0001c0001t0002g0186others(5): Show | 8 | HG01192.hp1 HG01516.hp2 HG02071.hp1 others(5): Show |
intron_variant | MODIFIER | c.916-791dupT | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr9 | 94453148 | |||||
| chr9:94453148
|
CT | C | 101 | a0001c0001t0001g0001a0001c0001t0001g0077a0001c0001t0001g0078others(98): Show | 103 | HG00323.hp1 HG00323.hp2 HG00408.hp2 others(100): Show |
intron_variant | MODIFIER | c.916-791delT | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr9 | 94453148 | |||||
| chr9:94453148
|
CTT | C | 121 | a0001c0001t0002g0218a0001c0001t0002g0219a0001c0001t0002g0220others(118): Show | 122 | HG00140.hp2 HG00544.hp1 HG00597.hp1 others(119): Show |
intron_variant | MODIFIER | c.916-792_916-791del others(2): Show |
MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr9 | 94453148 | |||||
| chr9:94453175
|
A | G | 2 | a0001c0001t0002g0039a0001c0001t0002g0040 | 2 | HG01516.hp1 HG01517.hp1 |
intron_variant | MODIFIER | c.916-783A>G | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 8/11 | chr9 | 94453175 | ||||||
| chr9:94453184
|
CTGTCACC others(10): Show |
C | 32 | a0001c0001t0001g0242a0001c0001t0001g0243a0001c0001t0001g0244others(29): Show | 32 | HG00408.hp2 HG00423.hp1 HG00423.hp2 others(29): Show |
intron_variant | MODIFIER | c.916-771_916-755del others(17): Show |
MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr9 | 94453184 | |||||
| chr9:94453335
|
C | A | 188 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0077others(185): Show | 192 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(189): Show |
intron_variant | MODIFIER | c.916-623C>A | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 8/11 | chr9 | 94453335 | ||||||
| chr9:94453336
|
G | A | 2 | a0001c0001t0003g0217a0001c0001t0003g0222 | 2 | HG01346.hp1 HG04228.hp1 |
intron_variant | MODIFIER | c.916-622G>A | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 8/11 | chr9 | 94453336 | ||||||
| chr9:94453342
|
G | T | 1 | a0001c0001t0004g0042 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.916-616G>T | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 8/11 | chr9 | 94453342 | ||||||
| chr9:94453479
|
A | G | 188 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0077others(185): Show | 192 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(189): Show |
intron_variant | MODIFIER | c.916-479A>G | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 8/11 | chr9 | 94453479 | ||||||
| chr9:94453562
|
C | T | 1 | a0001c0001t0003g0168 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.916-396C>T | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 8/11 | chr9 | 94453562 | ||||||
| chr9:94453694
|
C | T | 2 | a0001c0001t0008g0009a0001c0001t0008g0010 | 2 | HG02818.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.916-264C>T | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 8/11 | chr9 | 94453694 | ||||||
| chr9:94453760
|
G | T | 1 | a0001c0001t0001g0296 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.916-198G>T | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 8/11 | chr9 | 94453760 | ||||||
| chr9:94453881
|
G | T | 53 | a0001c0001t0004g0027a0001c0001t0004g0028a0001c0001t0004g0035others(50): Show | 54 | HG00597.hp1 HG00639.hp2 HG00642.hp1 others(51): Show |
intron_variant | MODIFIER | c.916-77G>T | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 8/11 | chr9 | 94453881 | ||||||
| chr9:94454170
|
G | C | 1 | a0001c0001t0001g0309 | 1 | NA18997.hp1 | intron_variant | MODIFIER | c.1028+100G>C | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 9/11 | chr9 | 94454170 | ||||||
| chr9:94454235
|
A | G | 1 | a0001c0001t0002g0341 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.1028+165A>G | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 9/11 | chr9 | 94454235 | ||||||
| chr9:94454259
|
A | G | 179 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0077others(176): Show | 183 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(180): Show |
intron_variant | MODIFIER | c.1028+189A>G | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 9/11 | chr9 | 94454259 | ||||||
| chr9:94454391
|
G | A | 89 | a0001c0001t0001g0001a0001c0001t0001g0225a0001c0001t0001g0226others(86): Show | 91 | HG00323.hp2 HG00408.hp2 HG00423.hp1 others(88): Show |
intron_variant | MODIFIER | c.1028+321G>A | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 9/11 | chr9 | 94454391 | ||||||
| chr9:94454416
|
G | T | 1 | a0001c0001t0003g0156 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.1028+346G>T | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 9/11 | chr9 | 94454416 | ||||||
| chr9:94454496
|
T | G | 1 | a0001c0001t0022g0201 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.1028+426T>G | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 9/11 | chr9 | 94454496 | ||||||
| chr9:94454529
|
G | GCTAATTT others(300): Show |
9 | a0001c0001t0007g0099a0001c0001t0007g0100a0001c0001t0007g0101others(6): Show | 9 | HG00544.hp1 HG01884.hp1 HG02630.hp1 others(6): Show |
intron_variant | MODIFIER | c.1028+476_1028+477i others(309): Show |
MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 9/11 | INFO_REALIGN_3_PRIME | chr9 | 94454529 | |||||
| chr9:94454568
|
G | A | 53 | a0001c0001t0004g0027a0001c0001t0004g0028a0001c0001t0004g0035others(50): Show | 54 | HG00597.hp1 HG00639.hp2 HG00642.hp1 others(51): Show |
intron_variant | MODIFIER | c.1028+498G>A | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 9/11 | chr9 | 94454568 | ||||||
| chr9:94454737
|
A | G | 3 | a0001c0001t0001g0268a0001c0001t0001g0272a0001c0001t0001g0273 | 3 | NA18939.hp1 NA18956.hp2 NA19084.hp2 |
intron_variant | MODIFIER | c.1028+667A>G | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 9/11 | chr9 | 94454737 | ||||||
| chr9:94454739
|
G | C | 67 | a0001c0001t0002g0029a0001c0001t0002g0036a0001c0001t0002g0039others(64): Show | 67 | HG00140.hp2 HG00544.hp1 HG00639.hp1 others(64): Show |
intron_variant | MODIFIER | c.1028+669G>C | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 9/11 | chr9 | 94454739 | ||||||
| chr9:94454752
|
A | G | 3 | a0001c0001t0002g0340a0001c0001t0002g0341a0001c0001t0002g0342 | 3 | HG01884.hp2 HG02886.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.1028+682A>G | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 9/11 | chr9 | 94454752 | ||||||
| chr9:94454957
|
G | A | 1 | a0001c0001t0002g0316 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.1028+887G>A | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 9/11 | chr9 | 94454957 | ||||||
| chr9:94454982
|
G | A | 176 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0077others(173): Show | 180 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(177): Show |
intron_variant | MODIFIER | c.1028+912G>A | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 9/11 | chr9 | 94454982 | ||||||
| chr9:94454993
|
G | A | 52 | a0001c0001t0004g0027a0001c0001t0004g0028a0001c0001t0004g0035others(49): Show | 53 | HG00597.hp1 HG00639.hp2 HG00642.hp1 others(50): Show |
intron_variant | MODIFIER | c.1028+923G>A | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 9/11 | chr9 | 94454993 | ||||||
| chr9:94455002
|
A | G | 1 | a0001c0001t0017g0022 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.1028+932A>G | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 9/11 | chr9 | 94455002 | ||||||
| chr9:94455039
|
A | G | 2 | a0001c0001t0001g0229a0001c0001t0017g0022 | 2 | HG02647.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.1028+969A>G | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 9/11 | chr9 | 94455039 | ||||||
| chr9:94455118
|
C | A | 3 | a0001c0001t0002g0321a0001c0001t0002g0322a0001c0001t0015g0006 | 3 | HG00639.hp1 HG01109.hp2 HG02683.hp1 |
intron_variant | MODIFIER | c.1028+1048C>A | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 9/11 | chr9 | 94455118 | ||||||
| chr9:94455156
|
C | CT | 55 | a0001c0001t0001g0225a0001c0001t0001g0226a0001c0001t0001g0228others(52): Show | 55 | HG00140.hp1 HG00438.hp2 HG00621.hp1 others(52): Show |
intron_variant | MODIFIER | c.1029-1059dupT | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 9/11 | INFO_REALIGN_3_PRIME | chr9 | 94455156 | |||||
| chr9:94455156
|
C | CTT | 17 | a0001c0001t0001g0229a0001c0001t0001g0237a0001c0001t0001g0245others(14): Show | 17 | HG00323.hp2 HG01071.hp2 HG01358.hp2 others(14): Show |
intron_variant | MODIFIER | c.1029-1060_1029-105 others(6): Show |
MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 9/11 | INFO_REALIGN_3_PRIME | chr9 | 94455156 | |||||
| chr9:94455156
|
C | CTTT | 35 | a0001c0001t0001g0001a0001c0001t0001g0242a0001c0001t0001g0244others(32): Show | 37 | HG00423.hp1 HG00423.hp2 HG00438.hp1 others(34): Show |
intron_variant | MODIFIER | c.1029-1061_1029-105 others(7): Show |
MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 9/11 | INFO_REALIGN_3_PRIME | chr9 | 94455156 | |||||
| chr9:94455156
|
C | CTTTT | 26 | a0001c0001t0001g0003a0001c0001t0001g0081a0001c0001t0001g0082others(23): Show | 27 | HG00099.hp2 HG00642.hp2 HG00733.hp2 others(24): Show |
intron_variant | MODIFIER | c.1029-1062_1029-105 others(8): Show |
MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 9/11 | INFO_REALIGN_3_PRIME | chr9 | 94455156 | |||||
| chr9:94455156
|
C | CTTTTTT | 11 | a0001c0001t0001g0090a0001c0001t0001g0094a0001c0001t0001g0292others(8): Show | 11 | HG00408.hp2 HG01256.hp2 HG02015.hp1 others(8): Show |
intron_variant | MODIFIER | c.1029-1064_1029-105 others(10): Show |
MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 9/11 | INFO_REALIGN_3_PRIME | chr9 | 94455156 | |||||
| chr9:94455156
|
C | CTTTTTTT others(1): Show |
16 | a0001c0001t0002g0318a0001c0001t0002g0321a0001c0001t0002g0322others(13): Show | 16 | HG00639.hp1 HG01109.hp2 HG01496.hp2 others(13): Show |
intron_variant | MODIFIER | c.1029-1066_1029-105 others(12): Show |
MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 9/11 | INFO_REALIGN_3_PRIME | chr9 | 94455156 | |||||
| chr9:94455156
|
C | CTTTTTTT others(2): Show |
16 | a0001c0001t0001g0087a0001c0001t0001g0296a0001c0001t0002g0319others(13): Show | 16 | HG00597.hp1 HG02572.hp2 HG02683.hp2 others(13): Show |
intron_variant | MODIFIER | c.1029-1067_1029-105 others(13): Show |
MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 9/11 | INFO_REALIGN_3_PRIME | chr9 | 94455156 | |||||
| chr9:94455156
|
C | CTTTTTTT others(3): Show |
8 | a0001c0001t0004g0042a0001c0001t0004g0046a0001c0001t0004g0057others(5): Show | 8 | HG01099.hp2 HG02148.hp2 HG02647.hp1 others(5): Show |
intron_variant | MODIFIER | c.1029-1068_1029-105 others(14): Show |
MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 9/11 | INFO_REALIGN_3_PRIME | chr9 | 94455156 | |||||
| chr9:94455156
|
C | CTTTTTTT others(4): Show |
8 | a0001c0001t0002g0317a0001c0001t0004g0067a0001c0001t0005g0020others(5): Show | 8 | HG00642.hp1 HG01109.hp1 HG01257.hp1 others(5): Show |
intron_variant | MODIFIER | c.1029-1069_1029-105 others(15): Show |
MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 9/11 | INFO_REALIGN_3_PRIME | chr9 | 94455156 | |||||
| chr9:94455156
|
C | CTTTTTTT others(5): Show |
12 | a0001c0001t0002g0039a0001c0001t0002g0040a0001c0001t0002g0316others(9): Show | 13 | HG00639.hp2 HG00733.hp1 HG01069.hp1 others(10): Show |
intron_variant | MODIFIER | c.1029-1070_1029-105 others(16): Show |
MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 9/11 | INFO_REALIGN_3_PRIME | chr9 | 94455156 | |||||
| chr9:94455156
|
C | CTTTTTTT others(6): Show |
8 | a0001c0001t0002g0029a0001c0001t0002g0036a0001c0001t0002g0315others(5): Show | 8 | HG01243.hp1 HG02040.hp2 HG02572.hp1 others(5): Show |
intron_variant | MODIFIER | c.1029-1071_1029-105 others(17): Show |
MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 9/11 | INFO_REALIGN_3_PRIME | chr9 | 94455156 | |||||
| chr9:94455156
|
C | CTTTTTTT others(7): Show |
1 | a0001c0001t0005g0030 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.1029-1072_1029-105 others(18): Show |
MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 9/11 | INFO_REALIGN_3_PRIME | chr9 | 94455156 | |||||
| chr9:94455156
|
C | CTTTTTTT others(8): Show |
1 | a0001c0001t0005g0075 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.1029-1073_1029-105 others(19): Show |
MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 9/11 | INFO_REALIGN_3_PRIME | chr9 | 94455156 | |||||
| chr9:94455156
|
C | CTTTTTTT others(16): Show |
2 | a0001c0001t0003g0007a0001c0001t0003g0008 | 2 | HG02615.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.1029-1081_1029-105 others(27): Show |
MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 9/11 | INFO_REALIGN_3_PRIME | chr9 | 94455156 | |||||
| chr9:94455169
|
TTTTTTTT others(7): Show |
T | 1 | a0001c0001t0002g0324 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.1029-1070_1029-105 others(18): Show |
MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 9/11 | chr9 | 94455169 | ||||||
| chr9:94455172
|
TTTTTTTT others(4): Show |
T | 2 | a0001c0001t0007g0103a0001c0001t0007g0223 | 2 | HG00544.hp1 HG03834.hp2 |
intron_variant | MODIFIER | c.1029-1067_1029-105 others(15): Show |
MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 9/11 | chr9 | 94455172 | ||||||
| chr9:94455182
|
G | T | 239 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0077others(236): Show | 243 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(240): Show |
intron_variant | MODIFIER | c.1029-1058G>T | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 9/11 | chr9 | 94455182 | ||||||
| chr9:94455183
|
A | T | 239 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0077others(236): Show | 243 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(240): Show |
intron_variant | MODIFIER | c.1029-1057A>T | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 9/11 | chr9 | 94455183 | ||||||
| chr9:94455317
|
C | T | 1 | a0001c0001t0003g0217 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.1029-923C>T | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 9/11 | chr9 | 94455317 | ||||||
| chr9:94455338
|
T | A | 4 | a0001c0001t0008g0014a0001c0001t0008g0015a0001c0001t0008g0016others(1): Show | 4 | HG01081.hp1 HG02559.hp1 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.1029-902T>A | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 9/11 | chr9 | 94455338 | ||||||
| chr9:94455338
|
T | C | 1 | a0001c0001t0002g0339 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.1029-902T>C | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 9/11 | chr9 | 94455338 | ||||||
| chr9:94455343
|
A | AT | 53 | a0001c0001t0002g0029a0001c0001t0002g0036a0001c0001t0002g0039others(50): Show | 53 | HG00140.hp2 HG00544.hp1 HG00639.hp1 others(50): Show |
intron_variant | MODIFIER | c.1029-887dupT | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 9/11 | INFO_REALIGN_3_PRIME | chr9 | 94455343 | |||||
| chr9:94455369
|
A | T | 36 | a0001c0001t0002g0029a0001c0001t0002g0036a0001c0001t0002g0039others(33): Show | 36 | HG00639.hp1 HG01109.hp2 HG01243.hp1 others(33): Show |
intron_variant | MODIFIER | c.1029-871A>T | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 9/11 | chr9 | 94455369 | ||||||
| chr9:94455378
|
A | AT | 23 | a0001c0001t0001g0003a0001c0001t0001g0081a0001c0001t0001g0086others(20): Show | 25 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(22): Show |
intron_variant | MODIFIER | c.1029-842dupT | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 9/11 | INFO_REALIGN_3_PRIME | chr9 | 94455378 | |||||
| chr9:94455378
|
A | ATTTT | 16 | a0001c0001t0004g0035a0001c0001t0004g0037a0001c0001t0004g0045others(13): Show | 17 | HG01069.hp1 HG01071.hp1 HG01081.hp2 others(14): Show |
intron_variant | MODIFIER | c.1029-845_1029-842d others(6): Show |
MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 9/11 | INFO_REALIGN_3_PRIME | chr9 | 94455378 | |||||
| chr9:94455378
|
A | ATTTTT | 36 | a0001c0001t0001g0229a0001c0001t0001g0308a0001c0001t0001g0310others(33): Show | 36 | HG00639.hp2 HG00642.hp1 HG00733.hp1 others(33): Show |
intron_variant | MODIFIER | c.1029-846_1029-842d others(7): Show |
MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 9/11 | INFO_REALIGN_3_PRIME | chr9 | 94455378 | |||||
| chr9:94455378
|
A | ATTTTTT | 76 | a0001c0001t0001g0001a0001c0001t0001g0225a0001c0001t0001g0226others(73): Show | 78 | HG00323.hp2 HG00408.hp2 HG00423.hp1 others(75): Show |
intron_variant | MODIFIER | c.1029-847_1029-842d others(8): Show |
MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 9/11 | INFO_REALIGN_3_PRIME | chr9 | 94455378 | |||||
| chr9:94455378
|
A | ATTTTTTT | 11 | a0001c0001t0001g0243a0001c0001t0001g0258a0001c0001t0001g0262others(8): Show | 11 | HG00621.hp1 HG02148.hp1 HG02258.hp2 others(8): Show |
intron_variant | MODIFIER | c.1029-848_1029-842d others(9): Show |
MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 9/11 | INFO_REALIGN_3_PRIME | chr9 | 94455378 | |||||
| chr9:94455378
|
A | ATTTTTTT others(7): Show |
3 | a0001c0001t0001g0077a0001c0001t0001g0078a0001c0001t0001g0079 | 3 | HG00323.hp1 HG02559.hp2 HG03942.hp2 |
intron_variant | MODIFIER | c.1029-855_1029-842d others(16): Show |
MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 9/11 | INFO_REALIGN_3_PRIME | chr9 | 94455378 | |||||
| chr9:94455378
|
A | ATTTTTTT others(8): Show |
2 | a0001c0001t0013g0023a0001c0001t0013g0024 | 2 | HG02040.hp2 HG02132.hp2 |
intron_variant | MODIFIER | c.1029-856_1029-842d others(17): Show |
MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 9/11 | INFO_REALIGN_3_PRIME | chr9 | 94455378 | |||||
| chr9:94455378
|
A | ATTTTTTT others(10): Show |
1 | a0001c0001t0001g0080 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.1029-858_1029-842d others(19): Show |
MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 9/11 | INFO_REALIGN_3_PRIME | chr9 | 94455378 | |||||
| chr9:94455378
|
AT | A | 34 | a0001c0001t0002g0029a0001c0001t0002g0036a0001c0001t0002g0039others(31): Show | 34 | HG00544.hp1 HG00741.hp1 HG01081.hp1 others(31): Show |
intron_variant | MODIFIER | c.1029-842delT | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 9/11 | INFO_REALIGN_3_PRIME | chr9 | 94455378 | |||||
| chr9:94455378
|
ATT | A | 24 | a0001c0001t0002g0316a0001c0001t0002g0318a0001c0001t0002g0319others(21): Show | 24 | HG00639.hp1 HG01109.hp2 HG01256.hp2 others(21): Show |
intron_variant | MODIFIER | c.1029-843_1029-842d others(4): Show |
MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 9/11 | INFO_REALIGN_3_PRIME | chr9 | 94455378 | |||||
| chr9:94455378
|
ATTTTTT | A | 6 | a0001c0001t0001g0084a0001c0001t0001g0085a0001c0001t0001g0089others(3): Show | 6 | HG01167.hp1 HG01169.hp1 HG01361.hp2 others(3): Show |
intron_variant | MODIFIER | c.1029-847_1029-842d others(8): Show |
MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 9/11 | INFO_REALIGN_3_PRIME | chr9 | 94455378 | |||||
| chr9:94456060
|
C | T | 179 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0077others(176): Show | 183 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(180): Show |
intron_variant | MODIFIER | c.1029-180C>T | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 9/11 | chr9 | 94456060 | ||||||
| chr9:94456364
|
T | C | 1 | a0001c0001t0008g0013 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.1126+27T>C | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 10/11 | chr9 | 94456364 | ||||||
| chr9:94456611
|
TTTC | T | 125 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0077others(122): Show | 128 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(125): Show |
intron_variant | MODIFIER | c.1126+280_1126+282d others(5): Show |
MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr9 | 94456611 | |||||
| chr9:94456774
|
T | C | 1 | a0001c0001t0003g0175 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.1126+437T>C | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 10/11 | chr9 | 94456774 | ||||||
| chr9:94456792
|
G | A | 1 | a0001c0001t0002g0341 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.1126+455G>A | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 10/11 | chr9 | 94456792 | ||||||
| chr9:94456834
|
A | G | 1 | a0001c0001t0017g0022 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.1126+497A>G | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 10/11 | chr9 | 94456834 | ||||||
| chr9:94456891
|
A | G | 180 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0077others(177): Show | 184 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(181): Show |
intron_variant | MODIFIER | c.1126+554A>G | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 10/11 | chr9 | 94456891 | ||||||
| chr9:94456969
|
A | AC | 21 | a0001c0001t0001g0082a0001c0001t0001g0243a0001c0001t0001g0245others(18): Show | 21 | HG00423.hp1 HG00423.hp2 HG00733.hp2 others(18): Show |
intron_variant | MODIFIER | c.1126+638dupC | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr9 | 94456969 | |||||
| chr9:94457053
|
G | A | 7 | a0001c0001t0002g0218a0001c0001t0002g0219a0001c0001t0002g0220others(4): Show | 7 | HG00140.hp1 HG01074.hp2 HG02602.hp2 others(4): Show |
intron_variant | MODIFIER | c.1126+716G>A | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 10/11 | chr9 | 94457053 | ||||||
| chr9:94457109
|
C | T | 23 | a0001c0001t0001g0003a0001c0001t0001g0077a0001c0001t0001g0078others(20): Show | 24 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(21): Show |
intron_variant | MODIFIER | c.1126+772C>T | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 10/11 | chr9 | 94457109 | ||||||
| chr9:94457213
|
C | T | 1 | a0001c0001t0001g0265 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.1126+876C>T | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 10/11 | chr9 | 94457213 | ||||||
| chr9:94457214
|
G | A | 8 | a0001c0001t0001g0269a0001c0001t0001g0277a0001c0001t0001g0278others(5): Show | 8 | HG00408.hp2 HG00438.hp1 HG01106.hp2 others(5): Show |
intron_variant | MODIFIER | c.1126+877G>A | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 10/11 | chr9 | 94457214 | ||||||
| chr9:94457396
|
CTTTT | C | 179 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0077others(176): Show | 183 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(180): Show |
intron_variant | MODIFIER | c.1127-921_1127-918d others(6): Show |
MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr9 | 94457396 | |||||
| chr9:94457404
|
T | A | 1 | a0001c0001t0003g0147 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.1127-918T>A | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 10/11 | chr9 | 94457404 | ||||||
| chr9:94457453
|
A | AT | 55 | a0001c0001t0004g0027a0001c0001t0004g0028a0001c0001t0004g0035others(52): Show | 56 | HG00597.hp1 HG00639.hp2 HG00642.hp1 others(53): Show |
intron_variant | MODIFIER | c.1127-859dupT | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr9 | 94457453 | |||||
| chr9:94457453
|
A | ATT | 122 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0077others(119): Show | 125 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(122): Show |
intron_variant | MODIFIER | c.1127-860_1127-859d others(4): Show |
MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr9 | 94457453 | |||||
| chr9:94457464
|
C | G | 11 | a0001c0001t0006g0107a0001c0001t0006g0108a0001c0001t0006g0109others(8): Show | 11 | HG01243.hp2 HG02109.hp1 HG02280.hp2 others(8): Show |
intron_variant | MODIFIER | c.1127-858C>G | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 10/11 | chr9 | 94457464 | ||||||
| chr9:94457470
|
C | T | 1 | a0001c0001t0004g0065 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.1127-852C>T | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 10/11 | chr9 | 94457470 | ||||||
| chr9:94457631
|
C | G | 1 | a0001c0001t0003g0176 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.1127-691C>G | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 10/11 | chr9 | 94457631 | ||||||
| chr9:94457635
|
G | T | 1 | a0001c0001t0003g0176 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.1127-687G>T | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 10/11 | chr9 | 94457635 | ||||||
| chr9:94457636
|
C | T | 1 | a0001c0001t0003g0176 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.1127-686C>T | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 10/11 | chr9 | 94457636 | ||||||
| chr9:94457637
|
C | T | 1 | a0001c0001t0003g0176 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.1127-685C>T | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 10/11 | chr9 | 94457637 | ||||||
| chr9:94457640
|
G | A | 1 | a0001c0001t0003g0176 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.1127-682G>A | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 10/11 | chr9 | 94457640 | ||||||
| chr9:94457641
|
G | T | 1 | a0001c0001t0003g0176 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.1127-681G>T | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 10/11 | chr9 | 94457641 | ||||||
| chr9:94457642
|
C | T | 1 | a0001c0001t0003g0176 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.1127-680C>T | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 10/11 | chr9 | 94457642 | ||||||
| chr9:94457644
|
T | A | 1 | a0001c0001t0003g0176 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.1127-678T>A | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 10/11 | chr9 | 94457644 | ||||||
| chr9:94457645
|
C | T | 1 | a0001c0001t0003g0176 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.1127-677C>T | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 10/11 | chr9 | 94457645 | ||||||
| chr9:94457647
|
G | A | 1 | a0001c0001t0003g0176 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.1127-675G>A | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 10/11 | chr9 | 94457647 | ||||||
| chr9:94457649
|
C | A | 1 | a0001c0001t0003g0176 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.1127-673C>A | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 10/11 | chr9 | 94457649 | ||||||
| chr9:94457650
|
A | T | 1 | a0001c0001t0003g0176 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.1127-672A>T | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 10/11 | chr9 | 94457650 | ||||||
| chr9:94457651
|
G | T | 1 | a0001c0001t0003g0176 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.1127-671G>T | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 10/11 | chr9 | 94457651 | ||||||
| chr9:94457653
|
C | T | 1 | a0001c0001t0003g0176 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.1127-669C>T | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 10/11 | chr9 | 94457653 | ||||||
| chr9:94457655
|
C | T | 1 | a0001c0001t0003g0176 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.1127-667C>T | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 10/11 | chr9 | 94457655 | ||||||
| chr9:94457656
|
C | T | 1 | a0001c0001t0003g0176 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.1127-666C>T | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 10/11 | chr9 | 94457656 | ||||||
| chr9:94457657
|
G | A | 1 | a0001c0001t0003g0176 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.1127-665G>A | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 10/11 | chr9 | 94457657 | ||||||
| chr9:94457659
|
C | T | 1 | a0001c0001t0003g0176 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.1127-663C>T | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 10/11 | chr9 | 94457659 | ||||||
| chr9:94457660
|
C | A | 1 | a0001c0001t0003g0176 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.1127-662C>A | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 10/11 | chr9 | 94457660 | ||||||
| chr9:94457662
|
G | T | 1 | a0001c0001t0003g0176 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.1127-660G>T | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 10/11 | chr9 | 94457662 | ||||||
| chr9:94457664
|
C | A | 1 | a0001c0001t0003g0176 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.1127-658C>A | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 10/11 | chr9 | 94457664 | ||||||
| chr9:94457666
|
T | A | 1 | a0001c0001t0003g0176 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.1127-656T>A | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 10/11 | chr9 | 94457666 | ||||||
| chr9:94457676
|
G | A | 1 | a0001c0001t0003g0176 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.1127-646G>A | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 10/11 | chr9 | 94457676 | ||||||
| chr9:94457677
|
G | A | 1 | a0001c0001t0003g0176 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.1127-645G>A | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 10/11 | chr9 | 94457677 | ||||||
| chr9:94457683
|
C | A | 1 | a0001c0001t0003g0176 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.1127-639C>A | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 10/11 | chr9 | 94457683 | ||||||
| chr9:94457685
|
T | G | 1 | a0001c0001t0003g0176 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.1127-637T>G | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 10/11 | chr9 | 94457685 | ||||||
| chr9:94457690
|
C | A | 1 | a0001c0001t0003g0176 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.1127-632C>A | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 10/11 | chr9 | 94457690 | ||||||
| chr9:94457726
|
G | A | 246 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0077others(243): Show | 250 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(247): Show |
intron_variant | MODIFIER | c.1127-596G>A | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 10/11 | chr9 | 94457726 | ||||||
| chr9:94457759
|
G | T | 19 | a0001c0001t0001g0003a0001c0001t0001g0081a0001c0001t0001g0082others(16): Show | 20 | HG00099.hp2 HG00280.hp2 HG00642.hp2 others(17): Show |
intron_variant | MODIFIER | c.1127-563G>T | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 10/11 | chr9 | 94457759 | ||||||
| chr9:94457949
|
G | C | 1 | a0001c0001t0002g0316 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.1127-373G>C | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 10/11 | chr9 | 94457949 | ||||||
| chr9:94458164
|
T | G | 2 | a0001c0001t0004g0056a0001c0001t0004g0062 | 2 | HG04228.hp2 NA20905.hp2 |
intron_variant | MODIFIER | c.1127-158T>G | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 10/11 | chr9 | 94458164 | ||||||
| chr9:94458203
|
T | TCTC | 247 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0077others(244): Show | 251 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(248): Show |
intron_variant | MODIFIER | c.1127-118_1127-116d others(5): Show |
MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr9 | 94458203 | |||||
| chr9:94458311
|
T | C | 4 | a0001c0001t0001g0088a0001c0001t0001g0092a0001c0001t0001g0097others(1): Show | 4 | HG00099.hp2 HG00280.hp2 HG01261.hp2 others(1): Show |
intron_variant | MODIFIER | c.1127-11T>C | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 10/11 | chr9 | 94458311 | ||||||
| chr9:94458577
|
G | C | 10 | a0001c0001t0008g0009a0001c0001t0008g0010a0001c0001t0008g0011others(7): Show | 10 | HG01081.hp1 HG02280.hp1 HG02559.hp1 others(7): Show |
intron_variant | MODIFIER | c.1269+113G>C | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 11/11 | chr9 | 94458577 | ||||||
| chr9:94458611
|
G | A | 1 | a0001c0001t0018g0041 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.1269+147G>A | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 11/11 | chr9 | 94458611 | ||||||
| chr9:94458664
|
T | TA | 136 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0077others(133): Show | 139 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(136): Show |
intron_variant | MODIFIER | c.1269+202dupA | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 11/11 | INFO_REALIGN_3_PRIME | chr9 | 94458664 | |||||
| chr9:94458731
|
G | A | 1 | a0001c0001t0003g0217 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.1269+267G>A | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 11/11 | chr9 | 94458731 | ||||||
| chr9:94458880
|
A | C | 1 | a0001c0001t0007g0101 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1270-281A>C | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 11/11 | chr9 | 94458880 | ||||||
| chr9:94459085
|
T | G | 3 | a0001c0001t0002g0218a0001c0001t0002g0219a0001c0001t0002g0220 | 3 | HG02818.hp1 HG03209.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.1270-76T>G | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 11/11 | chr9 | 94459085 | ||||||
| chr9:94459152
|
G | A | 179 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0077others(176): Show | 183 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(180): Show |
intron_variant | MODIFIER | c.1270-9G>A | MFSD14B | ENSG00000148110.17 | transcript | ENST00000375344.8 | protein_coding | 11/11 | chr9 | 94459152 |