Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| geneid | 9650 |
|---|---|
| ensemblid | ENSG00000066855.16 |
| hgncid | 29510 |
| symbol | MTFR1 |
| name | mitochondrial fission regulator 1 |
| refseq_nuc | NM_014637.4 |
| refseq_prot | NP_055452.3 |
| ensembl_nuc | ENST00000262146.9 |
| ensembl_prot | ENSP00000262146.4 |
| mane_status | MANE Select |
| chr | chr8 |
| start | 65644734 |
| end | 65710562 |
| strand | + |
| ver | v1.2 |
| region | chr8:65644734-65710562 |
| region5000 | chr8:65639734-65715562 |
| regionname0 | MTFR1_chr8_65644734_65710562 |
| regionname5000 | MTFR1_chr8_65639734_65715562 |
| thapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| t0001 | 1/1 | 1650 | 262 | 70 | 52 | 103 | 7 | 28 | MTFR1_chr8_65639734_65715562 | MTFR1 | copy fasta | chr8 | 65639734 | 65715562 |
| t0002 | 0/0 | 1650 | 33 | 3 | 10 | 10 | 6 | 4 | MTFR1_chr8_65639734_65715562 | MTFR1 | copy fasta | chr8 | 65639734 | 65715562 |
| t0003 | 0/0 | 1646 | 20 | 1 | 5 | 12 | 1 | 1 | MTFR1_chr8_65639734_65715562 | MTFR1 | copy fasta | chr8 | 65639734 | 65715562 |
| t0004 | 0/0 | 1650 | 14 | 0 | 2 | 12 | 0 | 0 | MTFR1_chr8_65639734_65715562 | MTFR1 | copy fasta | chr8 | 65639734 | 65715562 |
| t0005 | 0/0 | 1650 | 6 | 6 | 0 | 0 | 0 | 0 | MTFR1_chr8_65639734_65715562 | MTFR1 | copy fasta | chr8 | 65639734 | 65715562 |
| t0006 | 0/0 | 1650 | 3 | 0 | 2 | 0 | 0 | 1 | MTFR1_chr8_65639734_65715562 | MTFR1 | copy fasta | chr8 | 65639734 | 65715562 |
| t0007 | 0/0 | 1648 | 3 | 0 | 0 | 3 | 0 | 0 | MTFR1_chr8_65639734_65715562 | MTFR1 | copy fasta | chr8 | 65639734 | 65715562 |
| t0008 | 0/0 | 1650 | 3 | 3 | 0 | 0 | 0 | 0 | MTFR1_chr8_65639734_65715562 | MTFR1 | copy fasta | chr8 | 65639734 | 65715562 |
| t0009 | 0/0 | 1650 | 1 | 0 | 0 | 0 | 0 | 1 | MTFR1_chr8_65639734_65715562 | MTFR1 | copy fasta | chr8 | 65639734 | 65715562 |
| t0010 | 0/0 | 1650 | 1 | 0 | 1 | 0 | 0 | 0 | MTFR1_chr8_65639734_65715562 | MTFR1 | copy fasta | chr8 | 65639734 | 65715562 |
| t0011 | 0/0 | 1646 | 1 | 1 | 0 | 0 | 0 | 0 | MTFR1_chr8_65639734_65715562 | MTFR1 | copy fasta | chr8 | 65639734 | 65715562 |
| t0012 | 0/0 | 1650 | 1 | 0 | 0 | 0 | 0 | 1 | MTFR1_chr8_65639734_65715562 | MTFR1 | copy fasta | chr8 | 65639734 | 65715562 |
| ghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| g0001 | 0/0 | 2 | 1 | 0 | 0 | 1 | 0 | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| g0002 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| g0003 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| g0004 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| g0005 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| g0006 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| g0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| g0016 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| g0017 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| g0022 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| g0027 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| g0028 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| g0029 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| g0035 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| g0039 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| g0040 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| g0043 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| g0044 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| g0045 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| g0046 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| g0047 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| g0048 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| g0049 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| g0050 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| g0054 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| g0055 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| g0057 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| g0058 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| g0061 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| g0062 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| g0066 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| g0067 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| g0075 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| g0079 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| g0083 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| g0091 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| g0103 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| g0105 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| g0107 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| g0108 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| g0117 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| g0118 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| g0119 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| g0123 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| g0130 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| g0131 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| g0133 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| g0137 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| g0143 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| g0144 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| g0149 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| g0150 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| g0151 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| g0153 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| g0158 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| g0159 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| g0161 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| g0167 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| g0168 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| g0170 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| g0172 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| g0173 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| g0174 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| g0176 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| g0177 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| g0178 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| g0190 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| g0194 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| g0197 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| g0200 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| g0201 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| g0203 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| g0209 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| g0210 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| g0215 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| g0223 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| g0228 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| g0229 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| g0234 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| g0241 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| g0249 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| g0251 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| g0252 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| g0253 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| g0254 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| g0255 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| g0256 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| g0257 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| g0258 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| g0260 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| g0261 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| g0262 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| g0263 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| g0264 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| g0265 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| g0266 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| g0267 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| g0268 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| g0269 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| g0271 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| g0272 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| g0273 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| g0276 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| g0277 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| g0278 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| g0279 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| g0282 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| g0285 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| g0286 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| g0287 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| g0288 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| g0289 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| g0290 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| g0291 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| g0292 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| g0293 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| g0294 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| g0295 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| g0296 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| g0297 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| g0298 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| g0299 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| g0300 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| g0301 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| g0302 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| g0303 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| g0304 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| g0305 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| g0306 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| g0307 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| g0308 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| g0309 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| g0310 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| g0311 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| g0312 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| g0313 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| g0314 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| g0315 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| g0316 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| g0317 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| g0318 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| g0319 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| g0320 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| g0321 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| g0322 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| g0323 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| g0324 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| g0325 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| g0326 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| g0327 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| g0328 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| g0329 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| g0330 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| g0331 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| g0332 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| g0333 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| g0334 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| g0335 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| g0336 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| g0337 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| g0338 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| g0339 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| g0340 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| g0341 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| g0342 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| g0343 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| achapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 1002 | 347 | 84 | 72 | 139 | 14 | 36 | MTFR1_chr8_65639734_65715562 | MTFR1 | copy fasta | chr8 | 65639734 | 65715562 |
| a0002c0002 | 0/0 | 1002 | 1 | 0 | 0 | 1 | 0 | 0 | MTFR1_chr8_65639734_65715562 | MTFR1 | copy fasta | chr8 | 65639734 | 65715562 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 1/1 | 2651 | 262 | 70 | 52 | 103 | 7 | 28 | MTFR1_chr8_65639734_65715562 | MTFR1 | copy fasta | chr8 | 65639734 | 65715562 |
| a0001c0001t0002 | 0/0 | 2651 | 32 | 3 | 10 | 9 | 6 | 4 | MTFR1_chr8_65639734_65715562 | MTFR1 | copy fasta | chr8 | 65639734 | 65715562 |
| a0001c0001t0003 | 0/0 | 2647 | 20 | 1 | 5 | 12 | 1 | 1 | MTFR1_chr8_65639734_65715562 | MTFR1 | copy fasta | chr8 | 65639734 | 65715562 |
| a0001c0001t0004 | 0/0 | 2651 | 14 | 0 | 2 | 12 | 0 | 0 | MTFR1_chr8_65639734_65715562 | MTFR1 | copy fasta | chr8 | 65639734 | 65715562 |
| a0001c0001t0005 | 0/0 | 2651 | 6 | 6 | 0 | 0 | 0 | 0 | MTFR1_chr8_65639734_65715562 | MTFR1 | copy fasta | chr8 | 65639734 | 65715562 |
| a0001c0001t0006 | 0/0 | 2651 | 3 | 0 | 2 | 0 | 0 | 1 | MTFR1_chr8_65639734_65715562 | MTFR1 | copy fasta | chr8 | 65639734 | 65715562 |
| a0001c0001t0007 | 0/0 | 2649 | 3 | 0 | 0 | 3 | 0 | 0 | MTFR1_chr8_65639734_65715562 | MTFR1 | copy fasta | chr8 | 65639734 | 65715562 |
| a0001c0001t0008 | 0/0 | 2651 | 3 | 3 | 0 | 0 | 0 | 0 | MTFR1_chr8_65639734_65715562 | MTFR1 | copy fasta | chr8 | 65639734 | 65715562 |
| a0001c0001t0009 | 0/0 | 2651 | 1 | 0 | 0 | 0 | 0 | 1 | MTFR1_chr8_65639734_65715562 | MTFR1 | copy fasta | chr8 | 65639734 | 65715562 |
| a0001c0001t0010 | 0/0 | 2651 | 1 | 0 | 1 | 0 | 0 | 0 | MTFR1_chr8_65639734_65715562 | MTFR1 | copy fasta | chr8 | 65639734 | 65715562 |
| a0001c0001t0011 | 0/0 | 2647 | 1 | 1 | 0 | 0 | 0 | 0 | MTFR1_chr8_65639734_65715562 | MTFR1 | copy fasta | chr8 | 65639734 | 65715562 |
| a0001c0001t0012 | 0/0 | 2651 | 1 | 0 | 0 | 0 | 0 | 1 | MTFR1_chr8_65639734_65715562 | MTFR1 | copy fasta | chr8 | 65639734 | 65715562 |
| a0002c0002t0002 | 0/0 | 2651 | 1 | 0 | 0 | 1 | 0 | 0 | MTFR1_chr8_65639734_65715562 | MTFR1 | copy fasta | chr8 | 65639734 | 65715562 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0002 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| a0001c0001t0001g0003 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| a0001c0001t0001g0004 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| a0001c0001t0001g0005 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| a0001c0001t0001g0006 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| a0001c0001t0001g0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| a0001c0001t0001g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| a0001c0001t0001g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| a0001c0001t0001g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| a0001c0001t0001g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| a0001c0001t0001g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| a0001c0001t0001g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| a0001c0001t0001g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| a0001c0001t0001g0075 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| a0001c0001t0001g0079 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| a0001c0001t0001g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| a0001c0001t0001g0083 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| a0001c0001t0001g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| a0001c0001t0001g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| a0001c0001t0001g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| a0001c0001t0001g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| a0001c0001t0001g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| a0001c0001t0001g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| a0001c0001t0001g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| a0001c0001t0001g0091 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| a0001c0001t0001g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| a0001c0001t0001g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| a0001c0001t0001g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| a0001c0001t0001g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| a0001c0001t0001g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| a0001c0001t0001g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| a0001c0001t0001g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| a0001c0001t0001g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| a0001c0001t0001g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| a0001c0001t0001g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| a0001c0001t0001g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| a0001c0001t0001g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| a0001c0001t0001g0105 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| a0001c0001t0001g0107 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| a0001c0001t0001g0108 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| a0001c0001t0001g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| a0001c0001t0001g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| a0001c0001t0001g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| a0001c0001t0001g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| a0001c0001t0001g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| a0001c0001t0001g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| a0001c0001t0001g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| a0001c0001t0001g0119 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| a0001c0001t0001g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| a0001c0001t0001g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| a0001c0001t0001g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| a0001c0001t0001g0123 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| a0001c0001t0001g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| a0001c0001t0001g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| a0001c0001t0001g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| a0001c0001t0001g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| a0001c0001t0001g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| a0001c0001t0001g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| a0001c0001t0001g0130 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| a0001c0001t0001g0131 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| a0001c0001t0001g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| a0001c0001t0001g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| a0001c0001t0001g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| a0001c0001t0001g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| a0001c0001t0001g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| a0001c0001t0001g0143 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| a0001c0001t0001g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| a0001c0001t0001g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| a0001c0001t0001g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| a0001c0001t0001g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| a0001c0001t0001g0149 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| a0001c0001t0001g0150 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| a0001c0001t0001g0151 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| a0001c0001t0001g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| a0001c0001t0001g0153 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| a0001c0001t0001g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| a0001c0001t0001g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| a0001c0001t0001g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| a0001c0001t0001g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| a0001c0001t0001g0158 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| a0001c0001t0001g0159 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| a0001c0001t0001g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| a0001c0001t0001g0161 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| a0001c0001t0001g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| a0001c0001t0001g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| a0001c0001t0001g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| a0001c0001t0001g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| a0001c0001t0001g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| a0001c0001t0001g0167 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| a0001c0001t0001g0168 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| a0001c0001t0001g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| a0001c0001t0001g0170 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| a0001c0001t0001g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| a0001c0001t0001g0172 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| a0001c0001t0001g0173 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| a0001c0001t0001g0174 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| a0001c0001t0001g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| a0001c0001t0001g0176 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| a0001c0001t0001g0177 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| a0001c0001t0001g0178 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| a0001c0001t0001g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| a0001c0001t0001g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| a0001c0001t0001g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| a0001c0001t0001g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| a0001c0001t0001g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| a0001c0001t0001g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| a0001c0001t0001g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| a0001c0001t0001g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| a0001c0001t0001g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| a0001c0001t0001g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| a0001c0001t0001g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| a0001c0001t0001g0190 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| a0001c0001t0001g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| a0001c0001t0001g0194 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| a0001c0001t0001g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| a0001c0001t0001g0197 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| a0001c0001t0001g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| a0001c0001t0001g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| a0001c0001t0001g0200 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| a0001c0001t0001g0201 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| a0001c0001t0001g0203 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| a0001c0001t0001g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| a0001c0001t0001g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| a0001c0001t0001g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| a0001c0001t0001g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| a0001c0001t0001g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| a0001c0001t0001g0209 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| a0001c0001t0001g0210 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| a0001c0001t0001g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| a0001c0001t0001g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| a0001c0001t0001g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| a0001c0001t0001g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| a0001c0001t0001g0215 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| a0001c0001t0001g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| a0001c0001t0001g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| a0001c0001t0001g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| a0001c0001t0001g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| a0001c0001t0001g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| a0001c0001t0001g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| a0001c0001t0001g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| a0001c0001t0001g0223 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| a0001c0001t0001g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| a0001c0001t0001g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| a0001c0001t0001g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| a0001c0001t0001g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| a0001c0001t0001g0228 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| a0001c0001t0001g0229 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| a0001c0001t0001g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| a0001c0001t0001g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| a0001c0001t0001g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| a0001c0001t0001g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| a0001c0001t0001g0234 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| a0001c0001t0001g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| a0001c0001t0001g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| a0001c0001t0001g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| a0001c0001t0001g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| a0001c0001t0001g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| a0001c0001t0001g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| a0001c0001t0001g0241 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| a0001c0001t0001g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| a0001c0001t0001g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| a0001c0001t0001g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| a0001c0001t0001g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| a0001c0001t0001g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| a0001c0001t0001g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| a0001c0001t0001g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| a0001c0001t0001g0249 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| a0001c0001t0001g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| a0001c0001t0001g0251 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| a0001c0001t0001g0252 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| a0001c0001t0001g0253 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| a0001c0001t0001g0254 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| a0001c0001t0001g0255 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| a0001c0001t0001g0256 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| a0001c0001t0001g0257 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| a0001c0001t0001g0258 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| a0001c0001t0001g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| a0001c0001t0001g0260 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| a0001c0001t0001g0261 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| a0001c0001t0001g0262 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| a0001c0001t0001g0263 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| a0001c0001t0001g0264 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| a0001c0001t0001g0265 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| a0001c0001t0001g0266 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| a0001c0001t0001g0267 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| a0001c0001t0001g0268 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| a0001c0001t0001g0269 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| a0001c0001t0001g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| a0001c0001t0001g0271 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| a0001c0001t0001g0272 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| a0001c0001t0001g0273 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| a0001c0001t0001g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| a0001c0001t0001g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| a0001c0001t0001g0276 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| a0001c0001t0001g0277 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| a0001c0001t0001g0278 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| a0001c0001t0001g0279 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| a0001c0001t0001g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| a0001c0001t0001g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| a0001c0001t0001g0282 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| a0001c0001t0001g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| a0001c0001t0001g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| a0001c0001t0001g0285 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| a0001c0001t0001g0286 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| a0001c0001t0001g0287 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| a0001c0001t0001g0288 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| a0001c0001t0001g0289 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| a0001c0001t0001g0290 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| a0001c0001t0001g0291 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| a0001c0001t0001g0292 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| a0001c0001t0001g0293 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| a0001c0001t0001g0294 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| a0001c0001t0001g0295 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| a0001c0001t0001g0296 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| a0001c0001t0001g0297 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| a0001c0001t0001g0298 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| a0001c0001t0001g0299 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| a0001c0001t0001g0300 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| a0001c0001t0001g0301 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| a0001c0001t0001g0302 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| a0001c0001t0001g0303 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| a0001c0001t0001g0304 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| a0001c0001t0001g0305 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| a0001c0001t0001g0306 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| a0001c0001t0001g0307 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| a0001c0001t0001g0308 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| a0001c0001t0001g0309 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| a0001c0001t0001g0310 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| a0001c0001t0001g0311 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| a0001c0001t0001g0312 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| a0001c0001t0001g0313 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| a0001c0001t0001g0314 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| a0001c0001t0001g0315 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| a0001c0001t0001g0316 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| a0001c0001t0001g0317 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| a0001c0001t0001g0318 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| a0001c0001t0001g0319 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| a0001c0001t0001g0320 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| a0001c0001t0001g0321 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| a0001c0001t0001g0322 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| a0001c0001t0001g0323 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| a0001c0001t0001g0324 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| a0001c0001t0001g0325 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| a0001c0001t0001g0326 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| a0001c0001t0001g0327 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| a0001c0001t0001g0328 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| a0001c0001t0001g0329 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| a0001c0001t0001g0330 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| a0001c0001t0001g0331 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| a0001c0001t0001g0332 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| a0001c0001t0001g0333 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| a0001c0001t0001g0334 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| a0001c0001t0001g0335 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| a0001c0001t0001g0336 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| a0001c0001t0001g0337 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| a0001c0001t0001g0338 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| a0001c0001t0001g0339 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| a0001c0001t0001g0343 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| a0001c0001t0002g0001 | 0/0 | 2 | 1 | 0 | 0 | 1 | 0 | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| a0001c0001t0002g0039 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| a0001c0001t0002g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| a0001c0001t0002g0043 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| a0001c0001t0002g0044 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| a0001c0001t0002g0045 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| a0001c0001t0002g0046 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| a0001c0001t0002g0047 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| a0001c0001t0002g0048 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| a0001c0001t0002g0049 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| a0001c0001t0002g0050 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| a0001c0001t0002g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| a0001c0001t0002g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| a0001c0001t0002g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| a0001c0001t0002g0054 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| a0001c0001t0002g0055 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| a0001c0001t0002g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| a0001c0001t0002g0057 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| a0001c0001t0002g0058 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| a0001c0001t0002g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| a0001c0001t0002g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| a0001c0001t0002g0061 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| a0001c0001t0002g0062 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| a0001c0001t0002g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| a0001c0001t0002g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| a0001c0001t0002g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| a0001c0001t0002g0066 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| a0001c0001t0002g0067 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| a0001c0001t0002g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| a0001c0001t0002g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| a0001c0001t0002g0103 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| a0001c0001t0003g0016 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| a0001c0001t0003g0022 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| a0001c0001t0003g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| a0001c0001t0003g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| a0001c0001t0003g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| a0001c0001t0003g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| a0001c0001t0003g0027 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| a0001c0001t0003g0028 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| a0001c0001t0003g0029 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| a0001c0001t0003g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| a0001c0001t0003g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| a0001c0001t0003g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| a0001c0001t0003g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| a0001c0001t0003g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| a0001c0001t0003g0035 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| a0001c0001t0003g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| a0001c0001t0003g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| a0001c0001t0003g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| a0001c0001t0003g0040 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| a0001c0001t0003g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| a0001c0001t0004g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| a0001c0001t0004g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| a0001c0001t0004g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| a0001c0001t0004g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| a0001c0001t0004g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| a0001c0001t0004g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| a0001c0001t0004g0133 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| a0001c0001t0004g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| a0001c0001t0004g0137 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| a0001c0001t0004g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| a0001c0001t0004g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| a0001c0001t0004g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| a0001c0001t0004g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| a0001c0001t0004g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| a0001c0001t0005g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| a0001c0001t0005g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| a0001c0001t0005g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| a0001c0001t0005g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| a0001c0001t0005g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| a0001c0001t0005g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| a0001c0001t0006g0340 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| a0001c0001t0006g0341 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| a0001c0001t0006g0342 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| a0001c0001t0007g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| a0001c0001t0007g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| a0001c0001t0007g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| a0001c0001t0008g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| a0001c0001t0008g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| a0001c0001t0008g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| a0001c0001t0009g0117 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| a0001c0001t0010g0118 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| a0001c0001t0011g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| a0001c0001t0012g0144 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| a0002c0002t0002g0017 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0002 | g0062 | EUR | GBR | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| HG00099 | hp2 | a0001 | c0001 | t0001 | g0343 | EUR | GBR | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| HG00140 | hp1 | a0001 | c0001 | t0003 | g0016 | EUR | GBR | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| HG00140 | hp2 | a0001 | c0001 | t0002 | g0039 | EUR | GBR | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| HG00280 | hp1 | a0001 | c0001 | t0001 | g0091 | EUR | FIN | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| HG00280 | hp2 | a0001 | c0001 | t0002 | g0054 | EUR | FIN | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| HG00323 | hp1 | a0001 | c0001 | t0002 | g0044 | EUR | FIN | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| HG00323 | hp2 | a0001 | c0001 | t0001 | g0332 | EUR | FIN | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| HG00408 | hp1 | a0001 | c0001 | t0001 | g0240 | EAS | CHS | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| HG00408 | hp2 | a0001 | c0001 | t0001 | g0284 | EAS | CHS | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| HG00438 | hp1 | a0001 | c0001 | t0001 | g0124 | EAS | CHS | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| HG00438 | hp2 | a0001 | c0001 | t0004 | g0132 | EAS | CHS | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| HG00544 | hp1 | a0001 | c0001 | t0001 | g0280 | EAS | CHS | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| HG00544 | hp2 | a0001 | c0001 | t0001 | g0090 | EAS | CHS | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| HG00621 | hp1 | a0001 | c0001 | t0001 | g0102 | EAS | CHS | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| HG00621 | hp2 | a0001 | c0001 | t0001 | g0112 | EAS | CHS | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| HG00639 | hp1 | a0001 | c0001 | t0001 | g0320 | AMR | PUR | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| HG00639 | hp2 | a0001 | c0001 | t0001 | g0323 | AMR | PUR | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| HG00642 | hp1 | a0001 | c0001 | t0001 | g0119 | AMR | PUR | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| HG00642 | hp2 | a0001 | c0001 | t0003 | g0029 | AMR | PUR | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| HG00733 | hp1 | a0001 | c0001 | t0006 | g0342 | AMR | PUR | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| HG00733 | hp2 | a0001 | c0001 | t0002 | g0058 | AMR | PUR | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| HG00735 | hp1 | a0001 | c0001 | t0002 | g0067 | AMR | PUR | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| HG00735 | hp2 | a0001 | c0001 | t0001 | g0337 | AMR | PUR | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| HG00738 | hp1 | a0001 | c0001 | t0001 | g0004 | AMR | PUR | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| HG00738 | hp2 | a0001 | c0001 | t0001 | g0330 | AMR | PUR | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| HG00741 | hp1 | a0001 | c0001 | t0002 | g0048 | AMR | PUR | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| HG00741 | hp2 | a0001 | c0001 | t0001 | g0178 | AMR | PUR | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| HG01069 | hp1 | a0001 | c0001 | t0001 | g0339 | AMR | PUR | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| HG01069 | hp2 | a0001 | c0001 | t0001 | g0174 | AMR | PUR | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| HG01070 | hp1 | a0001 | c0001 | t0001 | g0329 | AMR | PUR | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| HG01070 | hp2 | a0001 | c0001 | t0001 | g0293 | AMR | PUR | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| HG01071 | hp1 | a0001 | c0001 | t0001 | g0297 | AMR | PUR | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| HG01071 | hp2 | a0001 | c0001 | t0001 | g0173 | AMR | PUR | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| HG01074 | hp1 | a0001 | c0001 | t0006 | g0341 | AMR | PUR | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| HG01074 | hp2 | a0001 | c0001 | t0001 | g0003 | AMR | PUR | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| HG01081 | hp1 | a0001 | c0001 | t0001 | g0334 | AMR | PUR | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| HG01081 | hp2 | a0001 | c0001 | t0001 | g0083 | AMR | PUR | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| HG01099 | hp1 | a0001 | c0001 | t0001 | g0326 | AMR | PUR | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| HG01099 | hp2 | a0001 | c0001 | t0004 | g0133 | AMR | PUR | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| HG01106 | hp1 | a0001 | c0001 | t0001 | g0321 | AMR | PUR | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| HG01106 | hp2 | a0001 | c0001 | t0001 | g0107 | AMR | PUR | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| HG01109 | hp1 | a0001 | c0001 | t0001 | g0228 | AMR | PUR | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| HG01109 | hp2 | a0001 | c0001 | t0002 | g0046 | AMR | PUR | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| HG01167 | hp1 | a0001 | c0001 | t0001 | g0229 | AMR | PUR | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| HG01167 | hp2 | a0001 | c0001 | t0001 | g0167 | AMR | PUR | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| HG01168 | hp1 | a0001 | c0001 | t0001 | g0261 | AMR | PUR | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| HG01168 | hp2 | a0001 | c0001 | t0003 | g0035 | AMR | PUR | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| HG01169 | hp1 | a0001 | c0001 | t0001 | g0004 | AMR | PUR | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| HG01169 | hp2 | a0001 | c0001 | t0001 | g0223 | AMR | PUR | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| HG01175 | hp1 | a0001 | c0001 | t0001 | g0318 | AMR | PUR | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| HG01175 | hp2 | a0001 | c0001 | t0002 | g0045 | AMR | PUR | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| HG01192 | hp1 | a0001 | c0001 | t0002 | g0047 | AMR | PUR | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| HG01192 | hp2 | a0001 | c0001 | t0001 | g0251 | AMR | PUR | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| HG01243 | hp1 | a0001 | c0001 | t0001 | g0234 | AMR | PUR | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| HG01243 | hp2 | a0001 | c0001 | t0001 | g0257 | AMR | PUR | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| HG01255 | hp1 | a0001 | c0001 | t0002 | g0057 | AMR | CLM | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| HG01255 | hp2 | a0001 | c0001 | t0001 | g0306 | AMR | CLM | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| HG01256 | hp1 | a0001 | c0001 | t0001 | g0317 | AMR | CLM | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| HG01256 | hp2 | a0001 | c0001 | t0001 | g0153 | AMR | CLM | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| HG01258 | hp1 | a0001 | c0001 | t0001 | g0260 | AMR | CLM | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| HG01258 | hp2 | a0001 | c0001 | t0001 | g0209 | AMR | CLM | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| HG01261 | hp1 | a0001 | c0001 | t0001 | g0322 | AMR | CLM | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| HG01261 | hp2 | a0001 | c0001 | t0001 | g0313 | AMR | CLM | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| HG01346 | hp1 | a0001 | c0001 | t0003 | g0027 | AMR | CLM | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| HG01346 | hp2 | a0001 | c0001 | t0001 | g0331 | AMR | CLM | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| HG01433 | hp1 | a0001 | c0001 | t0001 | g0316 | AMR | CLM | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| HG01433 | hp2 | a0001 | c0001 | t0001 | g0266 | AMR | CLM | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| HG01496 | hp1 | a0001 | c0001 | t0001 | g0190 | AMR | CLM | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| HG01496 | hp2 | a0001 | c0001 | t0003 | g0022 | AMR | CLM | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| HG01516 | hp1 | a0001 | c0001 | t0001 | g0325 | EUR | IBS | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| HG01516 | hp2 | a0001 | c0001 | t0002 | g0049 | EUR | IBS | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| HG01517 | hp1 | a0001 | c0001 | t0001 | g0324 | EUR | IBS | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| HG01517 | hp2 | a0001 | c0001 | t0001 | g0170 | EUR | IBS | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| HG01884 | hp1 | a0001 | c0001 | t0001 | g0235 | AFR | ACB | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| HG01884 | hp2 | a0001 | c0001 | t0001 | g0262 | AFR | ACB | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| HG01891 | hp1 | a0001 | c0001 | t0001 | g0307 | AFR | ACB | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| HG01891 | hp2 | a0001 | c0001 | t0001 | g0303 | AFR | ACB | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| HG01928 | hp1 | a0001 | c0001 | t0002 | g0066 | AMR | PEL | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| HG01928 | hp2 | a0001 | c0001 | t0001 | g0172 | AMR | PEL | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| HG01934 | hp1 | a0001 | c0001 | t0004 | g0137 | AMR | PEL | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| HG01934 | hp2 | a0001 | c0001 | t0001 | g0327 | AMR | PEL | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| HG01943 | hp1 | a0001 | c0001 | t0002 | g0043 | AMR | PEL | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| HG01943 | hp2 | a0001 | c0001 | t0001 | g0158 | AMR | PEL | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| HG01952 | hp1 | a0001 | c0001 | t0001 | g0116 | AMR | PEL | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| HG01952 | hp2 | a0001 | c0001 | t0001 | g0151 | AMR | PEL | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| HG02004 | hp1 | a0001 | c0001 | t0001 | g0159 | AMR | PEL | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| HG02004 | hp2 | a0001 | c0001 | t0002 | g0065 | AMR | PEL | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| HG02015 | hp1 | a0001 | c0001 | t0001 | g0126 | EAS | KHV | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| HG02015 | hp2 | a0001 | c0001 | t0001 | g0185 | EAS | KHV | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| HG02027 | hp1 | a0001 | c0001 | t0001 | g0100 | EAS | KHV | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| HG02027 | hp2 | a0001 | c0001 | t0001 | g0113 | EAS | KHV | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| HG02040 | hp1 | a0001 | c0001 | t0001 | g0165 | EAS | KHV | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| HG02040 | hp2 | a0001 | c0001 | t0002 | g0059 | EAS | KHV | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| HG02055 | hp1 | a0001 | c0001 | t0001 | g0009 | AFR | ACB | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| HG02055 | hp2 | a0001 | c0001 | t0001 | g0273 | AFR | ACB | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| HG02074 | hp1 | a0001 | c0001 | t0001 | g0283 | EAS | KHV | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| HG02074 | hp2 | a0001 | c0001 | t0001 | g0242 | EAS | KHV | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| HG02080 | hp1 | a0001 | c0001 | t0001 | g0244 | EAS | KHV | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| HG02080 | hp2 | a0001 | c0001 | t0004 | g0076 | EAS | KHV | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| HG02135 | hp1 | a0001 | c0001 | t0001 | g0163 | EAS | KHV | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| HG02135 | hp2 | a0001 | c0001 | t0004 | g0077 | EAS | KHV | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| HG02145 | hp1 | a0001 | c0001 | t0001 | g0254 | AFR | ACB | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| HG02145 | hp2 | a0001 | c0001 | t0001 | g0255 | AFR | ACB | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| HG02148 | hp1 | a0001 | c0001 | t0001 | g0335 | AMR | PEL | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| HG02148 | hp2 | a0001 | c0001 | t0001 | g0131 | AMR | PEL | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| HG02155 | hp1 | a0001 | c0001 | t0001 | g0122 | EAS | CDX | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| HG02155 | hp2 | a0001 | c0001 | t0001 | g0248 | EAS | CDX | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| HG02257 | hp1 | a0001 | c0001 | t0001 | g0278 | AFR | ACB | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| HG02257 | hp2 | a0001 | c0001 | t0001 | g0085 | AFR | ACB | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| HG02258 | hp1 | a0001 | c0001 | t0001 | g0294 | AFR | ACB | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| HG02258 | hp2 | a0001 | c0001 | t0001 | g0328 | AFR | ACB | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| HG02280 | hp1 | a0001 | c0001 | t0002 | g0001 | AFR | ACB | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| HG02280 | hp2 | a0001 | c0001 | t0001 | g0295 | AFR | ACB | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| HG02293 | hp1 | a0001 | c0001 | t0003 | g0040 | AMR | PEL | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| HG02293 | hp2 | a0001 | c0001 | t0001 | g0177 | AMR | PEL | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| HG02300 | hp1 | a0001 | c0001 | t0001 | g0338 | AMR | PEL | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| HG02300 | hp2 | a0001 | c0001 | t0010 | g0118 | AMR | PEL | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| HG02451 | hp1 | a0001 | c0001 | t0001 | g0269 | AFR | ACB | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| HG02451 | hp2 | a0001 | c0001 | t0001 | g0268 | AFR | ACB | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| HG02523 | hp1 | a0001 | c0001 | t0001 | g0160 | EAS | KHV | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| HG02523 | hp2 | a0001 | c0001 | t0001 | g0127 | EAS | KHV | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| HG02602 | hp1 | a0001 | c0001 | t0001 | g0176 | SAS | PJL | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| HG02602 | hp2 | a0001 | c0001 | t0002 | g0050 | SAS | PJL | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| HG02622 | hp1 | a0001 | c0001 | t0001 | g0249 | AFR | GWD | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| HG02622 | hp2 | a0001 | c0001 | t0001 | g0072 | AFR | GWD | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| HG02630 | hp1 | a0001 | c0001 | t0001 | g0304 | AFR | GWD | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| HG02630 | hp2 | a0001 | c0001 | t0001 | g0225 | AFR | GWD | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| HG02647 | hp1 | a0001 | c0001 | t0001 | g0256 | AFR | GWD | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| HG02647 | hp2 | a0001 | c0001 | t0005 | g0014 | AFR | GWD | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| HG02683 | hp1 | a0001 | c0001 | t0001 | g0282 | SAS | PJL | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| HG02683 | hp2 | a0001 | c0001 | t0001 | g0315 | SAS | PJL | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| HG02698 | hp1 | a0001 | c0001 | t0001 | g0279 | SAS | PJL | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| HG02698 | hp2 | a0001 | c0001 | t0002 | g0061 | SAS | PJL | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| HG02717 | hp1 | a0001 | c0001 | t0001 | g0302 | AFR | GWD | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| HG02717 | hp2 | a0001 | c0001 | t0001 | g0310 | AFR | GWD | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| HG02735 | hp1 | a0001 | c0001 | t0001 | g0203 | SAS | PJL | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| HG02735 | hp2 | a0001 | c0001 | t0001 | g0150 | SAS | PJL | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| HG02809 | hp1 | a0001 | c0001 | t0001 | g0272 | AFR | GWD | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| HG02809 | hp2 | a0001 | c0001 | t0001 | g0309 | AFR | GWD | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| HG02818 | hp1 | a0001 | c0001 | t0001 | g0250 | AFR | GWD | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| HG02818 | hp2 | a0001 | c0001 | t0001 | g0287 | AFR | GWD | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| HG02886 | hp1 | a0001 | c0001 | t0001 | g0301 | AFR | GWD | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| HG02886 | hp2 | a0001 | c0001 | t0001 | g0292 | AFR | GWD | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| HG02895 | hp1 | a0001 | c0001 | t0001 | g0189 | AFR | GWD | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| HG02895 | hp2 | a0001 | c0001 | t0001 | g0253 | AFR | GWD | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| HG02896 | hp1 | a0001 | c0001 | t0001 | g0263 | AFR | GWD | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| HG02896 | hp2 | a0001 | c0001 | t0001 | g0311 | AFR | GWD | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| HG02897 | hp1 | a0001 | c0001 | t0001 | g0264 | AFR | GWD | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| HG02897 | hp2 | a0001 | c0001 | t0001 | g0252 | AFR | GWD | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| HG02965 | hp1 | a0001 | c0001 | t0005 | g0021 | AFR | ESN | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| HG02965 | hp2 | a0001 | c0001 | t0001 | g0276 | AFR | ESN | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| HG02970 | hp1 | a0001 | c0001 | t0001 | g0071 | AFR | ESN | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| HG02970 | hp2 | a0001 | c0001 | t0001 | g0006 | AFR | ESN | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| HG02976 | hp1 | a0001 | c0001 | t0001 | g0289 | AFR | ESN | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| HG02976 | hp2 | a0001 | c0001 | t0001 | g0296 | AFR | ESN | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| HG03041 | hp1 | a0001 | c0001 | t0001 | g0265 | AFR | GWD | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| HG03041 | hp2 | a0001 | c0001 | t0001 | g0298 | AFR | GWD | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| HG03098 | hp1 | a0001 | c0001 | t0001 | g0300 | AFR | MSL | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| HG03098 | hp2 | a0001 | c0001 | t0001 | g0087 | AFR | MSL | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| HG03130 | hp1 | a0001 | c0001 | t0001 | g0008 | AFR | ESN | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| HG03130 | hp2 | a0001 | c0001 | t0008 | g0011 | AFR | ESN | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| HG03139 | hp1 | a0001 | c0001 | t0001 | g0238 | AFR | ESN | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| HG03139 | hp2 | a0001 | c0001 | t0001 | g0226 | AFR | ESN | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| HG03195 | hp1 | a0001 | c0001 | t0011 | g0070 | AFR | ESN | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| HG03195 | hp2 | a0001 | c0001 | t0001 | g0086 | AFR | ESN | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| HG03209 | hp1 | a0001 | c0001 | t0001 | g0073 | AFR | MSL | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| HG03209 | hp2 | a0001 | c0001 | t0001 | g0222 | AFR | MSL | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| HG03239 | hp1 | a0001 | c0001 | t0001 | g0201 | SAS | PJL | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| HG03239 | hp2 | a0001 | c0001 | t0001 | g0319 | SAS | PJL | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| HG03453 | hp1 | a0001 | c0001 | t0001 | g0258 | AFR | MSL | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| HG03453 | hp2 | a0001 | c0001 | t0001 | g0308 | AFR | MSL | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| HG03486 | hp1 | a0001 | c0001 | t0001 | g0224 | AFR | MSL | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| HG03486 | hp2 | a0001 | c0001 | t0001 | g0010 | AFR | MSL | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| HG03490 | hp1 | a0001 | c0001 | t0001 | g0197 | SAS | PJL | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| HG03490 | hp2 | a0001 | c0001 | t0001 | g0005 | SAS | PJL | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| HG03491 | hp1 | a0001 | c0001 | t0001 | g0285 | SAS | PJL | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| HG03491 | hp2 | a0001 | c0001 | t0001 | g0333 | SAS | PJL | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| HG03492 | hp1 | a0001 | c0001 | t0001 | g0200 | SAS | PJL | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| HG03492 | hp2 | a0001 | c0001 | t0001 | g0005 | SAS | PJL | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| HG03516 | hp1 | a0001 | c0001 | t0001 | g0141 | AFR | ESN | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| HG03516 | hp2 | a0001 | c0001 | t0001 | g0227 | AFR | ESN | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| HG03540 | hp1 | a0001 | c0001 | t0005 | g0020 | AFR | GWD | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| HG03540 | hp2 | a0001 | c0001 | t0001 | g0214 | AFR | GWD | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| HG03654 | hp1 | a0001 | c0001 | t0001 | g0079 | SAS | PJL | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| HG03654 | hp2 | a0001 | c0001 | t0001 | g0314 | SAS | PJL | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| HG03669 | hp1 | a0001 | c0001 | t0001 | g0194 | SAS | PJL | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| HG03669 | hp2 | a0001 | c0001 | t0001 | g0215 | SAS | PJL | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| HG03704 | hp1 | a0001 | c0001 | t0001 | g0336 | SAS | PJL | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| HG03704 | hp2 | a0001 | c0001 | t0001 | g0149 | SAS | PJL | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| HG03831 | hp1 | a0001 | c0001 | t0001 | g0123 | SAS | BEB | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| HG03831 | hp2 | a0001 | c0001 | t0001 | g0143 | SAS | BEB | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| HG03834 | hp1 | a0001 | c0001 | t0001 | g0075 | SAS | BEB | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| HG03834 | hp2 | a0001 | c0001 | t0002 | g0055 | SAS | BEB | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| HG03927 | hp1 | a0001 | c0001 | t0001 | g0105 | SAS | BEB | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| HG03927 | hp2 | a0001 | c0001 | t0001 | g0161 | SAS | BEB | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| HG04115 | hp1 | a0001 | c0001 | t0001 | g0108 | SAS | STU | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| HG04115 | hp2 | a0001 | c0001 | t0003 | g0028 | SAS | STU | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| HG04184 | hp1 | a0001 | c0001 | t0012 | g0144 | SAS | BEB | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| HG04184 | hp2 | a0001 | c0001 | t0002 | g0103 | SAS | BEB | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| HG04204 | hp1 | a0001 | c0001 | t0006 | g0340 | SAS | STU | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| HG04204 | hp2 | a0001 | c0001 | t0009 | g0117 | SAS | STU | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| HG04228 | hp1 | a0001 | c0001 | t0001 | g0130 | SAS | STU | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| HG04228 | hp2 | a0001 | c0001 | t0001 | g0312 | SAS | STU | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| NA18522 | hp1 | a0001 | c0001 | t0001 | g0230 | AFR | YRI | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| NA18522 | hp2 | a0001 | c0001 | t0001 | g0305 | AFR | YRI | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| NA18612 | hp1 | a0001 | c0001 | t0001 | g0164 | EAS | CHB | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| NA18612 | hp2 | a0001 | c0001 | t0001 | g0145 | EAS | CHB | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| NA18906 | hp1 | a0001 | c0001 | t0001 | g0007 | AFR | YRI | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| NA18906 | hp2 | a0001 | c0001 | t0005 | g0019 | AFR | YRI | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| NA18939 | hp1 | a0001 | c0001 | t0003 | g0023 | EAS | JPT | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| NA18939 | hp2 | a0001 | c0001 | t0004 | g0082 | EAS | JPT | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| NA18942 | hp1 | a0001 | c0001 | t0003 | g0033 | EAS | JPT | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| NA18942 | hp2 | a0001 | c0001 | t0002 | g0042 | EAS | JPT | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| NA18944 | hp1 | a0001 | c0001 | t0001 | g0196 | EAS | JPT | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| NA18944 | hp2 | a0001 | c0001 | t0001 | g0095 | EAS | JPT | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| NA18945 | hp1 | a0001 | c0001 | t0001 | g0111 | EAS | JPT | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| NA18945 | hp2 | a0001 | c0001 | t0001 | g0152 | EAS | JPT | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| NA18946 | hp1 | a0001 | c0001 | t0003 | g0034 | EAS | JPT | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| NA18946 | hp2 | a0001 | c0001 | t0001 | g0206 | EAS | JPT | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| NA18947 | hp1 | a0001 | c0001 | t0001 | g0237 | EAS | JPT | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| NA18947 | hp2 | a0001 | c0001 | t0001 | g0134 | EAS | JPT | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| NA18950 | hp1 | a0001 | c0001 | t0004 | g0202 | EAS | JPT | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| NA18950 | hp2 | a0001 | c0001 | t0001 | g0187 | EAS | JPT | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| NA18951 | hp1 | a0001 | c0001 | t0003 | g0038 | EAS | JPT | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| NA18951 | hp2 | a0001 | c0001 | t0001 | g0129 | EAS | JPT | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| NA18954 | hp1 | a0001 | c0001 | t0001 | g0231 | EAS | JPT | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| NA18954 | hp2 | a0001 | c0001 | t0004 | g0078 | EAS | JPT | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| NA18956 | hp1 | a0001 | c0001 | t0001 | g0233 | EAS | JPT | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| NA18956 | hp2 | a0001 | c0001 | t0001 | g0198 | EAS | JPT | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| NA18957 | hp1 | a0001 | c0001 | t0007 | g0193 | EAS | JPT | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| NA18957 | hp2 | a0001 | c0001 | t0001 | g0097 | EAS | JPT | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| NA18959 | hp1 | a0001 | c0001 | t0001 | g0270 | EAS | JPT | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| NA18959 | hp2 | a0001 | c0001 | t0001 | g0243 | EAS | JPT | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| NA18960 | hp1 | a0001 | c0001 | t0001 | g0138 | EAS | JPT | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| NA18960 | hp2 | a0001 | c0001 | t0001 | g0162 | EAS | JPT | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| NA18965 | hp1 | a0001 | c0001 | t0001 | g0246 | EAS | JPT | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| NA18965 | hp2 | a0001 | c0001 | t0003 | g0031 | EAS | JPT | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| NA18967 | hp1 | a0001 | c0001 | t0001 | g0182 | EAS | JPT | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| NA18967 | hp2 | a0001 | c0001 | t0003 | g0026 | EAS | JPT | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| NA18970 | hp1 | a0001 | c0001 | t0001 | g0074 | EAS | JPT | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| NA18970 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| NA18971 | hp1 | a0001 | c0001 | t0001 | g0099 | EAS | JPT | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| NA18971 | hp2 | a0001 | c0001 | t0001 | g0114 | EAS | JPT | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| NA18977 | hp1 | a0001 | c0001 | t0001 | g0128 | EAS | JPT | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| NA18977 | hp2 | a0001 | c0001 | t0003 | g0032 | EAS | JPT | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| NA18979 | hp1 | a0001 | c0001 | t0001 | g0220 | EAS | JPT | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| NA18979 | hp2 | a0001 | c0001 | t0004 | g0139 | EAS | JPT | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| NA18980 | hp1 | a0001 | c0001 | t0001 | g0169 | EAS | JPT | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| NA18980 | hp2 | a0001 | c0001 | t0004 | g0135 | EAS | JPT | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| NA18985 | hp1 | a0001 | c0001 | t0001 | g0184 | EAS | JPT | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| NA18985 | hp2 | a0001 | c0001 | t0001 | g0096 | EAS | JPT | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| NA18986 | hp1 | a0001 | c0001 | t0001 | g0213 | EAS | JPT | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| NA18986 | hp2 | a0001 | c0001 | t0001 | g0221 | EAS | JPT | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| NA18987 | hp1 | a0001 | c0001 | t0001 | g0147 | EAS | JPT | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| NA18987 | hp2 | a0001 | c0001 | t0001 | g0125 | EAS | JPT | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| NA18989 | hp1 | a0001 | c0001 | t0001 | g0247 | EAS | JPT | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| NA18989 | hp2 | a0001 | c0001 | t0002 | g0053 | EAS | JPT | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| NA18990 | hp1 | a0001 | c0001 | t0001 | g0094 | EAS | JPT | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| NA18990 | hp2 | a0001 | c0001 | t0001 | g0188 | EAS | JPT | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| NA18993 | hp1 | a0001 | c0001 | t0001 | g0275 | EAS | JPT | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| NA18993 | hp2 | a0001 | c0001 | t0001 | g0180 | EAS | JPT | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| NA18994 | hp1 | a0001 | c0001 | t0007 | g0106 | EAS | JPT | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| NA18994 | hp2 | a0001 | c0001 | t0001 | g0093 | EAS | JPT | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| NA18995 | hp1 | a0001 | c0001 | t0001 | g0217 | EAS | JPT | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| NA18995 | hp2 | a0001 | c0001 | t0001 | g0204 | EAS | JPT | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| NA18997 | hp1 | a0001 | c0001 | t0002 | g0063 | EAS | JPT | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| NA18997 | hp2 | a0001 | c0001 | t0001 | g0281 | EAS | JPT | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| NA18999 | hp1 | a0001 | c0001 | t0001 | g0186 | EAS | JPT | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| NA18999 | hp2 | a0001 | c0001 | t0001 | g0110 | EAS | JPT | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| NA19001 | hp1 | a0001 | c0001 | t0003 | g0030 | EAS | JPT | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| NA19001 | hp2 | a0001 | c0001 | t0007 | g0115 | EAS | JPT | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| NA19002 | hp1 | a0001 | c0001 | t0001 | g0084 | EAS | JPT | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| NA19002 | hp2 | a0001 | c0001 | t0001 | g0098 | EAS | JPT | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| NA19003 | hp1 | a0001 | c0001 | t0004 | g0195 | EAS | JPT | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| NA19003 | hp2 | a0001 | c0001 | t0001 | g0089 | EAS | JPT | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| NA19005 | hp1 | a0001 | c0001 | t0001 | g0218 | EAS | JPT | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| NA19005 | hp2 | a0001 | c0001 | t0001 | g0121 | EAS | JPT | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| NA19009 | hp1 | a0001 | c0001 | t0002 | g0052 | EAS | JPT | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| NA19009 | hp2 | a0001 | c0001 | t0001 | g0179 | EAS | JPT | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| NA19011 | hp1 | a0001 | c0001 | t0004 | g0081 | EAS | JPT | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| NA19011 | hp2 | a0001 | c0001 | t0001 | g0148 | EAS | JPT | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| NA19043 | hp1 | a0001 | c0001 | t0001 | g0286 | AFR | LWK | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| NA19043 | hp2 | a0001 | c0001 | t0008 | g0012 | AFR | LWK | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| NA19056 | hp1 | a0001 | c0001 | t0004 | g0140 | EAS | JPT | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| NA19056 | hp2 | a0001 | c0001 | t0003 | g0037 | EAS | JPT | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| NA19058 | hp1 | a0001 | c0001 | t0001 | g0157 | EAS | JPT | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| NA19058 | hp2 | a0001 | c0001 | t0001 | g0080 | EAS | JPT | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| NA19060 | hp1 | a0001 | c0001 | t0001 | g0120 | EAS | JPT | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| NA19060 | hp2 | a0001 | c0001 | t0001 | g0166 | EAS | JPT | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| NA19065 | hp1 | a0001 | c0001 | t0002 | g0051 | EAS | JPT | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| NA19065 | hp2 | a0001 | c0001 | t0001 | g0212 | EAS | JPT | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| NA19066 | hp1 | a0001 | c0001 | t0001 | g0216 | EAS | JPT | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| NA19066 | hp2 | a0001 | c0001 | t0001 | g0181 | EAS | JPT | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| NA19067 | hp1 | a0001 | c0001 | t0001 | g0274 | EAS | JPT | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| NA19067 | hp2 | a0001 | c0001 | t0001 | g0146 | EAS | JPT | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| NA19068 | hp1 | a0001 | c0001 | t0001 | g0239 | EAS | JPT | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| NA19068 | hp2 | a0001 | c0001 | t0001 | g0232 | EAS | JPT | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| NA19070 | hp1 | a0001 | c0001 | t0001 | g0142 | EAS | JPT | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| NA19070 | hp2 | a0001 | c0001 | t0001 | g0156 | EAS | JPT | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| NA19074 | hp1 | a0001 | c0001 | t0001 | g0155 | EAS | JPT | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| NA19074 | hp2 | a0001 | c0001 | t0002 | g0060 | EAS | JPT | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| NA19077 | hp1 | a0001 | c0001 | t0001 | g0205 | EAS | JPT | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| NA19077 | hp2 | a0001 | c0001 | t0001 | g0207 | EAS | JPT | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| NA19078 | hp1 | a0001 | c0001 | t0001 | g0259 | EAS | JPT | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| NA19078 | hp2 | a0001 | c0001 | t0001 | g0175 | EAS | JPT | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| NA19079 | hp1 | a0001 | c0001 | t0001 | g0171 | EAS | JPT | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| NA19079 | hp2 | a0001 | c0001 | t0002 | g0056 | EAS | JPT | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| NA19080 | hp1 | a0001 | c0001 | t0001 | g0088 | EAS | JPT | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| NA19080 | hp2 | a0001 | c0001 | t0002 | g0064 | EAS | JPT | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| NA19081 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| NA19081 | hp2 | a0001 | c0001 | t0003 | g0025 | EAS | JPT | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| NA19082 | hp1 | a0001 | c0001 | t0004 | g0191 | EAS | JPT | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| NA19082 | hp2 | a0001 | c0001 | t0001 | g0092 | EAS | JPT | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| NA19084 | hp1 | a0001 | c0001 | t0001 | g0208 | EAS | JPT | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| NA19084 | hp2 | a0001 | c0001 | t0001 | g0192 | EAS | JPT | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| NA19085 | hp1 | a0001 | c0001 | t0001 | g0219 | EAS | JPT | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| NA19085 | hp2 | a0001 | c0001 | t0001 | g0136 | EAS | JPT | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| NA19086 | hp1 | a0001 | c0001 | t0001 | g0199 | EAS | JPT | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| NA19086 | hp2 | a0001 | c0001 | t0003 | g0036 | EAS | JPT | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| NA19088 | hp1 | a0002 | c0002 | t0002 | g0017 | EAS | JPT | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| NA19088 | hp2 | a0001 | c0001 | t0001 | g0211 | EAS | JPT | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| NA19091 | hp1 | a0001 | c0001 | t0003 | g0024 | EAS | JPT | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| NA19091 | hp2 | a0001 | c0001 | t0001 | g0109 | EAS | JPT | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| NA19240 | hp1 | a0001 | c0001 | t0001 | g0277 | AFR | YRI | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| NA19240 | hp2 | a0001 | c0001 | t0002 | g0069 | AFR | YRI | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| NA20129 | hp1 | a0001 | c0001 | t0001 | g0290 | AFR | ASW | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| NA20129 | hp2 | a0001 | c0001 | t0001 | g0154 | AFR | ASW | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| NA20752 | hp1 | a0001 | c0001 | t0001 | g0003 | EUR | TSI | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| NA20752 | hp2 | a0001 | c0001 | t0002 | g0001 | EUR | TSI | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| HG01123 | hp1 | a0001 | c0001 | t0001 | g0288 | AMR | CLM | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| HG01123 | hp2 | a0001 | c0001 | t0001 | g0168 | AMR | CLM | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| HG02109 | hp1 | a0001 | c0001 | t0001 | g0101 | AFR | ACB | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| HG02109 | hp2 | a0001 | c0001 | t0002 | g0068 | AFR | ACB | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| HG02486 | hp1 | a0001 | c0001 | t0008 | g0013 | AFR | ACB | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| HG02486 | hp2 | a0001 | c0001 | t0001 | g0271 | AFR | ACB | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| HG02559 | hp1 | a0001 | c0001 | t0001 | g0291 | AFR | ACB | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| HG02559 | hp2 | a0001 | c0001 | t0001 | g0104 | AFR | ACB | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| HG03471 | hp1 | a0001 | c0001 | t0001 | g0299 | AFR | MSL | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| HG03471 | hp2 | a0001 | c0001 | t0003 | g0041 | AFR | MSL | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| HG06807 | hp1 | a0001 | c0001 | t0001 | g0267 | AFR | USA | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| HG06807 | hp2 | a0001 | c0001 | t0005 | g0015 | AFR | USA | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| NA18955 | hp1 | a0001 | c0001 | t0001 | g0245 | EAS | JPT | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| NA18955 | hp2 | a0001 | c0001 | t0001 | g0236 | EAS | JPT | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| NA20300 | hp1 | a0001 | c0001 | t0005 | g0018 | AFR | USA | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| NA20300 | hp2 | a0001 | c0001 | t0001 | g0183 | AFR | USA | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0001 | g0210 | REF | REF | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| homoSapiens_grch38 | hp1 | a0001 | c0001 | t0001 | g0241 | REF | REF | MTFR1_chr8_65639734_65715562 | MTFR1 | chr8 | 65639734 | 65715562 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr8:65704905
|
C | T | 1 | a0002 | 1 | NA19088.hp1 | stop_gained | HIGH | c.493C>T | p.Gln165* | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 5/8 | 624/2651 | 493/1002 | 165/333 | chr8 | 65704905 |
| 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 |
|---|
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr8:65709045
|
T | C | 1 | a0001c0001t0009 | 1 | HG04204.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1T>C | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 8/8 | 1 | chr8 | 65709045 | |||||
| chr8:65709176
|
G | A | 1 | a0001c0001t0006 | 3 | HG00733.hp1 HG01074.hp1 HG04204.hp1 |
3_prime_UTR_variant | MODIFIER | c.*132G>A | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 8/8 | 132 | chr8 | 65709176 | |||||
| chr8:65709330
|
A | G | 1 | a0001c0001t0005 | 6 | HG02647.hp2 HG02965.hp1 HG03540.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*286A>G | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 8/8 | 286 | chr8 | 65709330 | |||||
| chr8:65709438
|
A | C | 1 | a0001c0001t0012 | 1 | HG04184.hp1 | 3_prime_UTR_variant | MODIFIER | c.*394A>C | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 8/8 | 394 | chr8 | 65709438 | |||||
| chr8:65709479
|
CGTTT | C | 2 | a0001c0001t0003a0001c0001t0011 | 21 | HG00140.hp1 HG00642.hp2 HG01168.hp2 others(18): Show |
3_prime_UTR_variant | MODIFIER | c.*440_*443delGTTT | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 8/8 | 440 | INFO_REALIGN_3_PRIME | chr8 | 65709479 | ||||
| chr8:65709557
|
G | C | 1 | a0001c0001t0004 | 14 | HG00438.hp2 HG01099.hp2 HG01934.hp1 others(11): Show |
3_prime_UTR_variant | MODIFIER | c.*513G>C | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 8/8 | 513 | chr8 | 65709557 | |||||
| chr8:65709786
|
T | C | 1 | a0001c0001t0011 | 1 | HG03195.hp1 | 3_prime_UTR_variant | MODIFIER | c.*742T>C | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 8/8 | 742 | chr8 | 65709786 | |||||
| chr8:65710001
|
C | T | 6 | a0001c0001t0002a0001c0001t0003a0001c0001t0005others(3): Show | 63 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(60): Show |
3_prime_UTR_variant | MODIFIER | c.*957C>T | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 8/8 | 957 | chr8 | 65710001 | |||||
| chr8:65710416
|
T | G | 1 | a0001c0001t0010 | 1 | HG02300.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1372T>G | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 8/8 | 1372 | chr8 | 65710416 | |||||
| chr8:65710439
|
C | T | 2 | a0001c0001t0005a0001c0001t0008 | 9 | HG02486.hp1 HG02647.hp2 HG02965.hp1 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*1395C>T | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 8/8 | 1395 | chr8 | 65710439 | |||||
| chr8:65710544
|
CTG | C | 1 | a0001c0001t0007 | 3 | NA18957.hp1 NA18994.hp1 NA19001.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1502_*1503delGT | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 8/8 | 1502 | INFO_REALIGN_3_PRIME | chr8 | 65710544 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr8:65644824
|
G | A | 5 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008others(2): Show | 5 | HG02055.hp1 HG02970.hp2 HG03130.hp1 others(2): Show |
intron_variant | MODIFIER | c.-81+40G>A | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 1/7 | chr8 | 65644824 | ||||||
| chr8:65645030
|
G | A | 66 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008others(63): Show | 67 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(64): Show |
intron_variant | MODIFIER | c.-81+246G>A | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 1/7 | chr8 | 65645030 | ||||||
| chr8:65645044
|
G | T | 1 | a0001c0001t0001g0343 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.-81+260G>T | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 1/7 | chr8 | 65645044 | ||||||
| chr8:65645114
|
T | A | 3 | a0001c0001t0008g0011a0001c0001t0008g0012a0001c0001t0008g0013 | 3 | HG02486.hp1 HG03130.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.-81+330T>A | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 1/7 | chr8 | 65645114 | ||||||
| chr8:65645297
|
C | T | 3 | a0001c0001t0006g0340a0001c0001t0006g0341a0001c0001t0006g0342 | 3 | HG00733.hp1 HG01074.hp1 HG04204.hp1 |
intron_variant | MODIFIER | c.-81+513C>T | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 1/7 | chr8 | 65645297 | ||||||
| chr8:65645298
|
T | C | 68 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008others(65): Show | 69 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(66): Show |
intron_variant | MODIFIER | c.-81+514T>C | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 1/7 | chr8 | 65645298 | ||||||
| chr8:65645422
|
A | G | 1 | a0001c0001t0001g0339 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.-81+638A>G | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 1/7 | chr8 | 65645422 | ||||||
| chr8:65645587
|
G | A | 69 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008others(66): Show | 70 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(67): Show |
intron_variant | MODIFIER | c.-81+803G>A | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 1/7 | chr8 | 65645587 | ||||||
| chr8:65645631
|
T | G | 69 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008others(66): Show | 70 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(67): Show |
intron_variant | MODIFIER | c.-81+847T>G | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 1/7 | chr8 | 65645631 | ||||||
| chr8:65645689
|
C | CT | 44 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008others(41): Show | 45 | HG00099.hp1 HG00280.hp2 HG00639.hp1 others(42): Show |
intron_variant | MODIFIER | c.-81+908dupT | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr8 | 65645689 | |||||
| chr8:65645689
|
C | CTT | 13 | a0001c0001t0002g0039a0001c0001t0002g0044a0001c0001t0002g0045others(10): Show | 13 | HG00140.hp2 HG00323.hp1 HG00741.hp1 others(10): Show |
intron_variant | MODIFIER | c.-81+907_-81+908dup others(2): Show |
MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr8 | 65645689 | |||||
| chr8:65645692
|
T | TC | 34 | a0001c0001t0001g0004a0001c0001t0001g0205a0001c0001t0001g0206others(31): Show | 35 | HG00738.hp1 HG01074.hp1 HG01109.hp1 others(32): Show |
intron_variant | MODIFIER | c.-81+922dupC | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr8 | 65645692 | |||||
| chr8:65645692
|
T | TCC | 52 | a0001c0001t0001g0003a0001c0001t0001g0141a0001c0001t0001g0142others(49): Show | 53 | HG00741.hp2 HG01069.hp2 HG01071.hp2 others(50): Show |
intron_variant | MODIFIER | c.-81+921_-81+922dup others(2): Show |
MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr8 | 65645692 | |||||
| chr8:65645692
|
T | TCCC | 16 | a0001c0001t0001g0002a0001c0001t0001g0088a0001c0001t0001g0089others(13): Show | 17 | HG00280.hp1 HG00544.hp2 HG01069.hp1 others(14): Show |
intron_variant | MODIFIER | c.-81+920_-81+922dup others(3): Show |
MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr8 | 65645692 | |||||
| chr8:65645692
|
T | TTC | 3 | a0001c0001t0001g0312a0001c0001t0001g0313a0001c0001t0001g0314 | 3 | HG01261.hp2 HG03654.hp2 HG04228.hp2 |
intron_variant | MODIFIER | c.-81+908_-81+909ins others(2): Show |
MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 1/7 | chr8 | 65645692 | ||||||
| chr8:65645692
|
T | TTTC | 10 | a0001c0001t0003g0022a0001c0001t0003g0023a0001c0001t0003g0024others(7): Show | 10 | HG00642.hp2 HG01346.hp1 HG01496.hp2 others(7): Show |
intron_variant | MODIFIER | c.-81+908_-81+909ins others(3): Show |
MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 1/7 | chr8 | 65645692 | ||||||
| chr8:65645692
|
TC | T | 14 | a0001c0001t0001g0303a0001c0001t0001g0304a0001c0001t0001g0305others(11): Show | 14 | HG01255.hp2 HG01891.hp1 HG01891.hp2 others(11): Show |
intron_variant | MODIFIER | c.-81+922delC | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr8 | 65645692 | |||||
| chr8:65645693
|
C | T | 49 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(46): Show | 51 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(48): Show |
intron_variant | MODIFIER | c.-81+909C>T | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 1/7 | chr8 | 65645693 | ||||||
| chr8:65645694
|
C | T | 27 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008others(24): Show | 28 | HG00099.hp1 HG00280.hp2 HG00733.hp2 others(25): Show |
intron_variant | MODIFIER | c.-81+910C>T | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 1/7 | chr8 | 65645694 | ||||||
| chr8:65645705
|
C | CCCCCG | 17 | a0001c0001t0001g0071a0001c0001t0001g0072a0001c0001t0001g0073others(14): Show | 17 | HG01081.hp2 HG02080.hp2 HG02135.hp2 others(14): Show |
intron_variant | MODIFIER | c.-81+922_-81+923ins others(5): Show |
MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr8 | 65645705 | |||||
| chr8:65645705
|
C | CCCCG | 39 | a0001c0001t0001g0102a0001c0001t0001g0104a0001c0001t0001g0105others(36): Show | 39 | HG00438.hp1 HG00438.hp2 HG00621.hp1 others(36): Show |
intron_variant | MODIFIER | c.-81+922_-81+923ins others(4): Show |
MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr8 | 65645705 | |||||
| chr8:65645705
|
C | CCCG | 14 | a0001c0001t0001g0192a0001c0001t0001g0194a0001c0001t0001g0196others(11): Show | 14 | HG02735.hp1 HG03239.hp1 HG03490.hp1 others(11): Show |
intron_variant | MODIFIER | c.-81+922_-81+923ins others(3): Show |
MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr8 | 65645705 | |||||
| chr8:65645745
|
C | G | 1 | a0001c0001t0001g0190 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.-81+961C>G | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 1/7 | chr8 | 65645745 | ||||||
| chr8:65645917
|
T | C | 1 | a0001c0001t0001g0328 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.-81+1133T>C | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 1/7 | chr8 | 65645917 | ||||||
| chr8:65645965
|
T | C | 3 | a0001c0001t0006g0340a0001c0001t0006g0341a0001c0001t0006g0342 | 3 | HG00733.hp1 HG01074.hp1 HG04204.hp1 |
intron_variant | MODIFIER | c.-81+1181T>C | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 1/7 | chr8 | 65645965 | ||||||
| chr8:65646025
|
G | C | 1 | a0001c0001t0001g0102 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.-81+1241G>C | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 1/7 | chr8 | 65646025 | ||||||
| chr8:65646035
|
A | G | 3 | a0001c0001t0001g0085a0001c0001t0001g0086a0001c0001t0001g0087 | 3 | HG02257.hp2 HG03098.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.-81+1251A>G | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 1/7 | chr8 | 65646035 | ||||||
| chr8:65646138
|
C | T | 10 | a0001c0001t0001g0293a0001c0001t0001g0294a0001c0001t0001g0295others(7): Show | 10 | HG01070.hp2 HG01071.hp1 HG02258.hp1 others(7): Show |
intron_variant | MODIFIER | c.-81+1354C>T | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 1/7 | chr8 | 65646138 | ||||||
| chr8:65646180
|
C | T | 8 | a0001c0001t0001g0189a0001c0001t0001g0234a0001c0001t0001g0235others(5): Show | 8 | HG01243.hp1 HG01884.hp1 HG02559.hp1 others(5): Show |
intron_variant | MODIFIER | c.-81+1396C>T | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 1/7 | chr8 | 65646180 | ||||||
| chr8:65646293
|
A | G | 7 | a0001c0001t0001g0184a0001c0001t0001g0185a0001c0001t0001g0186others(4): Show | 7 | HG02015.hp2 NA18950.hp2 NA18956.hp1 others(4): Show |
intron_variant | MODIFIER | c.-81+1509A>G | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 1/7 | chr8 | 65646293 | ||||||
| chr8:65646596
|
G | C | 9 | a0001c0001t0005g0014a0001c0001t0005g0015a0001c0001t0005g0018others(6): Show | 9 | HG02486.hp1 HG02647.hp2 HG02965.hp1 others(6): Show |
intron_variant | MODIFIER | c.-81+1812G>C | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 1/7 | chr8 | 65646596 | ||||||
| chr8:65646774
|
C | T | 69 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008others(66): Show | 70 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(67): Show |
intron_variant | MODIFIER | c.-81+1990C>T | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 1/7 | chr8 | 65646774 | ||||||
| chr8:65646792
|
A | G | 1 | a0001c0001t0001g0288 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.-81+2008A>G | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 1/7 | chr8 | 65646792 | ||||||
| chr8:65646994
|
G | A | 69 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008others(66): Show | 70 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(67): Show |
intron_variant | MODIFIER | c.-81+2210G>A | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 1/7 | chr8 | 65646994 | ||||||
| chr8:65647070
|
A | G | 1 | a0001c0001t0001g0101 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.-81+2286A>G | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 1/7 | chr8 | 65647070 | ||||||
| chr8:65647173
|
A | G | 47 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(44): Show | 48 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(45): Show |
intron_variant | MODIFIER | c.-81+2389A>G | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 1/7 | chr8 | 65647173 | ||||||
| chr8:65647299
|
G | C | 10 | a0001c0001t0001g0293a0001c0001t0001g0294a0001c0001t0001g0295others(7): Show | 10 | HG01070.hp2 HG01071.hp1 HG02258.hp1 others(7): Show |
intron_variant | MODIFIER | c.-81+2515G>C | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 1/7 | chr8 | 65647299 | ||||||
| chr8:65647301
|
T | C | 1 | a0001c0001t0001g0141 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.-81+2517T>C | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 1/7 | chr8 | 65647301 | ||||||
| chr8:65647584
|
A | G | 1 | a0001c0001t0001g0287 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.-81+2800A>G | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 1/7 | chr8 | 65647584 | ||||||
| chr8:65647806
|
CA | C | 255 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0006others(252): Show | 258 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(255): Show |
intron_variant | MODIFIER | c.-81+3033delA | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr8 | 65647806 | |||||
| chr8:65647809
|
A | C | 1 | a0001c0001t0001g0231 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.-81+3025A>C | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 1/7 | chr8 | 65647809 | ||||||
| chr8:65647823
|
C | A | 1 | a0001c0001t0001g0339 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.-81+3039C>A | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 1/7 | chr8 | 65647823 | ||||||
| chr8:65647997
|
A | ATTTG | 22 | a0001c0001t0001g0222a0001c0001t0001g0249a0001c0001t0001g0250others(19): Show | 22 | HG01070.hp2 HG01071.hp1 HG01192.hp2 others(19): Show |
intron_variant | MODIFIER | c.-81+3241_-81+3244d others(6): Show |
MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr8 | 65647997 | |||||
| chr8:65647997
|
ATTTG | A | 3 | a0001c0001t0001g0085a0001c0001t0001g0086a0001c0001t0001g0087 | 3 | HG02257.hp2 HG03098.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.-81+3241_-81+3244d others(6): Show |
MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr8 | 65647997 | |||||
| chr8:65648152
|
G | T | 1 | a0001c0001t0001g0233 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.-81+3368G>T | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 1/7 | chr8 | 65648152 | ||||||
| chr8:65648167
|
C | G | 3 | a0001c0001t0008g0011a0001c0001t0008g0012a0001c0001t0008g0013 | 3 | HG02486.hp1 HG03130.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.-81+3383C>G | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 1/7 | chr8 | 65648167 | ||||||
| chr8:65648241
|
T | A | 1 | a0001c0001t0001g0142 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.-81+3457T>A | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 1/7 | chr8 | 65648241 | ||||||
| chr8:65648253
|
G | A | 2 | a0001c0001t0002g0049a0001c0001t0002g0050 | 2 | HG01516.hp2 HG02602.hp2 |
intron_variant | MODIFIER | c.-81+3469G>A | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 1/7 | chr8 | 65648253 | ||||||
| chr8:65648310
|
C | T | 1 | a0001c0001t0001g0343 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.-81+3526C>T | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 1/7 | chr8 | 65648310 | ||||||
| chr8:65648547
|
A | G | 78 | a0001c0001t0001g0071a0001c0001t0001g0072a0001c0001t0001g0073others(75): Show | 78 | HG00408.hp2 HG00438.hp1 HG00438.hp2 others(75): Show |
intron_variant | MODIFIER | c.-81+3763A>G | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 1/7 | chr8 | 65648547 | ||||||
| chr8:65648559
|
G | A | 3 | a0001c0001t0001g0205a0001c0001t0001g0236a0001c0001t0001g0237 | 3 | NA18947.hp1 NA18955.hp2 NA19077.hp1 |
intron_variant | MODIFIER | c.-81+3775G>A | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 1/7 | chr8 | 65648559 | ||||||
| chr8:65648608
|
T | A | 64 | a0001c0001t0002g0001a0001c0001t0002g0039a0001c0001t0002g0042others(61): Show | 65 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(62): Show |
intron_variant | MODIFIER | c.-81+3824T>A | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 1/7 | chr8 | 65648608 | ||||||
| chr8:65648626
|
G | T | 64 | a0001c0001t0002g0001a0001c0001t0002g0039a0001c0001t0002g0042others(61): Show | 65 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(62): Show |
intron_variant | MODIFIER | c.-81+3842G>T | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 1/7 | chr8 | 65648626 | ||||||
| chr8:65648639
|
C | T | 64 | a0001c0001t0002g0001a0001c0001t0002g0039a0001c0001t0002g0042others(61): Show | 65 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(62): Show |
intron_variant | MODIFIER | c.-81+3855C>T | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 1/7 | chr8 | 65648639 | ||||||
| chr8:65648640
|
G | A | 1 | a0001c0001t0001g0259 | 1 | NA19078.hp1 | intron_variant | MODIFIER | c.-81+3856G>A | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 1/7 | chr8 | 65648640 | ||||||
| chr8:65648662
|
A | G | 3 | a0001c0001t0006g0340a0001c0001t0006g0341a0001c0001t0006g0342 | 3 | HG00733.hp1 HG01074.hp1 HG04204.hp1 |
intron_variant | MODIFIER | c.-81+3878A>G | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 1/7 | chr8 | 65648662 | ||||||
| chr8:65648666
|
G | A | 64 | a0001c0001t0002g0001a0001c0001t0002g0039a0001c0001t0002g0042others(61): Show | 65 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(62): Show |
intron_variant | MODIFIER | c.-81+3882G>A | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 1/7 | chr8 | 65648666 | ||||||
| chr8:65648699
|
T | C | 64 | a0001c0001t0002g0001a0001c0001t0002g0039a0001c0001t0002g0042others(61): Show | 65 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(62): Show |
intron_variant | MODIFIER | c.-81+3915T>C | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 1/7 | chr8 | 65648699 | ||||||
| chr8:65648867
|
G | T | 1 | a0001c0001t0001g0276 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.-81+4083G>T | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 1/7 | chr8 | 65648867 | ||||||
| chr8:65649040
|
T | A | 1 | a0001c0001t0001g0143 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.-81+4256T>A | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 1/7 | chr8 | 65649040 | ||||||
| chr8:65649064
|
TAAAAC | T | 64 | a0001c0001t0002g0001a0001c0001t0002g0039a0001c0001t0002g0042others(61): Show | 65 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(62): Show |
intron_variant | MODIFIER | c.-81+4283_-81+4287d others(7): Show |
MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr8 | 65649064 | |||||
| chr8:65649115
|
T | C | 1 | a0001c0001t0012g0144 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.-81+4331T>C | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 1/7 | chr8 | 65649115 | ||||||
| chr8:65649253
|
C | A | 61 | a0001c0001t0002g0001a0001c0001t0002g0039a0001c0001t0002g0042others(58): Show | 62 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(59): Show |
intron_variant | MODIFIER | c.-81+4469C>A | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 1/7 | chr8 | 65649253 | ||||||
| chr8:65649273
|
C | T | 64 | a0001c0001t0002g0001a0001c0001t0002g0039a0001c0001t0002g0042others(61): Show | 65 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(62): Show |
intron_variant | MODIFIER | c.-81+4489C>T | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 1/7 | chr8 | 65649273 | ||||||
| chr8:65649309
|
C | T | 1 | a0001c0001t0001g0310 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.-81+4525C>T | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 1/7 | chr8 | 65649309 | ||||||
| chr8:65649317
|
T | C | 64 | a0001c0001t0002g0001a0001c0001t0002g0039a0001c0001t0002g0042others(61): Show | 65 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(62): Show |
intron_variant | MODIFIER | c.-81+4533T>C | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 1/7 | chr8 | 65649317 | ||||||
| chr8:65649341
|
C | T | 1 | a0001c0001t0001g0338 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.-81+4557C>T | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 1/7 | chr8 | 65649341 | ||||||
| chr8:65649463
|
T | C | 64 | a0001c0001t0002g0001a0001c0001t0002g0039a0001c0001t0002g0042others(61): Show | 65 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(62): Show |
intron_variant | MODIFIER | c.-81+4679T>C | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 1/7 | chr8 | 65649463 | ||||||
| chr8:65649524
|
T | A | 26 | a0001c0001t0001g0005a0001c0001t0001g0223a0001c0001t0001g0260others(23): Show | 27 | HG00099.hp2 HG00323.hp2 HG00639.hp1 others(24): Show |
intron_variant | MODIFIER | c.-81+4740T>A | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 1/7 | chr8 | 65649524 | ||||||
| chr8:65649875
|
G | A | 65 | a0001c0001t0002g0001a0001c0001t0002g0039a0001c0001t0002g0042others(62): Show | 66 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(63): Show |
intron_variant | MODIFIER | c.-81+5091G>A | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 1/7 | chr8 | 65649875 | ||||||
| chr8:65649899
|
C | T | 19 | a0001c0001t0001g0002a0001c0001t0001g0094a0001c0001t0001g0095others(16): Show | 20 | HG01167.hp1 HG02027.hp1 HG02055.hp2 others(17): Show |
intron_variant | MODIFIER | c.-81+5115C>T | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 1/7 | chr8 | 65649899 | ||||||
| chr8:65649900
|
G | A | 3 | a0001c0001t0001g0085a0001c0001t0001g0086a0001c0001t0001g0087 | 3 | HG02257.hp2 HG03098.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.-81+5116G>A | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 1/7 | chr8 | 65649900 | ||||||
| chr8:65650066
|
C | T | 2 | a0001c0001t0001g0235a0001c0001t0001g0292 | 2 | HG01884.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.-81+5282C>T | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 1/7 | chr8 | 65650066 | ||||||
| chr8:65650135
|
A | C | 6 | a0001c0001t0001g0179a0001c0001t0001g0180a0001c0001t0001g0181others(3): Show | 6 | HG02155.hp2 NA18954.hp1 NA18967.hp1 others(3): Show |
intron_variant | MODIFIER | c.-81+5351A>C | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 1/7 | chr8 | 65650135 | ||||||
| chr8:65650210
|
C | CT | 8 | a0001c0001t0001g0084a0001c0001t0001g0092a0001c0001t0001g0093others(5): Show | 8 | HG02451.hp1 HG04184.hp1 NA18979.hp2 others(5): Show |
intron_variant | MODIFIER | c.-81+5447dupT | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr8 | 65650210 | |||||
| chr8:65650210
|
CT | C | 92 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0007others(89): Show | 93 | HG00140.hp1 HG00642.hp2 HG01070.hp1 others(90): Show |
intron_variant | MODIFIER | c.-81+5447delT | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr8 | 65650210 | |||||
| chr8:65650210
|
CTT | C | 39 | a0001c0001t0001g0229a0001c0001t0001g0249a0001c0001t0001g0250others(36): Show | 40 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(37): Show |
intron_variant | MODIFIER | c.-81+5446_-81+5447d others(4): Show |
MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr8 | 65650210 | |||||
| chr8:65650258
|
C | T | 62 | a0001c0001t0002g0001a0001c0001t0002g0039a0001c0001t0002g0042others(59): Show | 63 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(60): Show |
intron_variant | MODIFIER | c.-81+5474C>T | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 1/7 | chr8 | 65650258 | ||||||
| chr8:65650280
|
C | T | 3 | a0001c0001t0006g0340a0001c0001t0006g0341a0001c0001t0006g0342 | 3 | HG00733.hp1 HG01074.hp1 HG04204.hp1 |
intron_variant | MODIFIER | c.-81+5496C>T | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 1/7 | chr8 | 65650280 | ||||||
| chr8:65650317
|
G | A | 1 | a0001c0001t0001g0330 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.-81+5533G>A | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 1/7 | chr8 | 65650317 | ||||||
| chr8:65650435
|
G | C | 1 | a0001c0001t0001g0270 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.-81+5651G>C | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 1/7 | chr8 | 65650435 | ||||||
| chr8:65650462
|
G | A | 22 | a0001c0001t0001g0222a0001c0001t0001g0249a0001c0001t0001g0250others(19): Show | 22 | HG01070.hp2 HG01071.hp1 HG01192.hp2 others(19): Show |
intron_variant | MODIFIER | c.-81+5678G>A | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 1/7 | chr8 | 65650462 | ||||||
| chr8:65650467
|
T | C | 65 | a0001c0001t0002g0001a0001c0001t0002g0039a0001c0001t0002g0042others(62): Show | 66 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(63): Show |
intron_variant | MODIFIER | c.-81+5683T>C | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 1/7 | chr8 | 65650467 | ||||||
| chr8:65650479
|
C | T | 1 | a0001c0001t0001g0138 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.-81+5695C>T | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 1/7 | chr8 | 65650479 | ||||||
| chr8:65650833
|
C | T | 10 | a0001c0001t0001g0293a0001c0001t0001g0294a0001c0001t0001g0295others(7): Show | 10 | HG01070.hp2 HG01071.hp1 HG02258.hp1 others(7): Show |
intron_variant | MODIFIER | c.-81+6049C>T | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 1/7 | chr8 | 65650833 | ||||||
| chr8:65651000
|
T | TG | 65 | a0001c0001t0002g0001a0001c0001t0002g0039a0001c0001t0002g0042others(62): Show | 66 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(63): Show |
intron_variant | MODIFIER | c.-81+6219dupG | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr8 | 65651000 | |||||
| chr8:65651115
|
A | C | 1 | a0001c0001t0001g0083 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.-81+6331A>C | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 1/7 | chr8 | 65651115 | ||||||
| chr8:65651302
|
TGA | T | 65 | a0001c0001t0002g0001a0001c0001t0002g0039a0001c0001t0002g0042others(62): Show | 66 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(63): Show |
intron_variant | MODIFIER | c.-81+6519_-81+6520d others(4): Show |
MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 1/7 | chr8 | 65651302 | ||||||
| chr8:65651348
|
T | G | 10 | a0001c0001t0001g0293a0001c0001t0001g0294a0001c0001t0001g0295others(7): Show | 10 | HG01070.hp2 HG01071.hp1 HG02258.hp1 others(7): Show |
intron_variant | MODIFIER | c.-81+6564T>G | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 1/7 | chr8 | 65651348 | ||||||
| chr8:65651403
|
A | G | 1 | a0001c0001t0001g0286 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.-81+6619A>G | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 1/7 | chr8 | 65651403 | ||||||
| chr8:65651657
|
A | T | 32 | a0001c0001t0002g0001a0001c0001t0002g0039a0001c0001t0002g0042others(29): Show | 33 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(30): Show |
intron_variant | MODIFIER | c.-81+6873A>T | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 1/7 | chr8 | 65651657 | ||||||
| chr8:65651702
|
G | A | 9 | a0001c0001t0005g0014a0001c0001t0005g0015a0001c0001t0005g0018others(6): Show | 9 | HG02486.hp1 HG02647.hp2 HG02965.hp1 others(6): Show |
intron_variant | MODIFIER | c.-81+6918G>A | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 1/7 | chr8 | 65651702 | ||||||
| chr8:65651963
|
A | AT | 44 | a0001c0001t0002g0001a0001c0001t0002g0039a0001c0001t0002g0042others(41): Show | 45 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(42): Show |
intron_variant | MODIFIER | c.-81+7192dupT | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr8 | 65651963 | |||||
| chr8:65651963
|
A | ATT | 21 | a0001c0001t0003g0016a0001c0001t0003g0022a0001c0001t0003g0023others(18): Show | 21 | HG00140.hp1 HG00642.hp2 HG01168.hp2 others(18): Show |
intron_variant | MODIFIER | c.-81+7191_-81+7192d others(4): Show |
MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr8 | 65651963 | |||||
| chr8:65652006
|
C | T | 19 | a0001c0001t0001g0002a0001c0001t0001g0094a0001c0001t0001g0095others(16): Show | 20 | HG01167.hp1 HG02027.hp1 HG02055.hp2 others(17): Show |
intron_variant | MODIFIER | c.-81+7222C>T | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 1/7 | chr8 | 65652006 | ||||||
| chr8:65652158
|
G | C | 22 | a0001c0001t0001g0222a0001c0001t0001g0249a0001c0001t0001g0250others(19): Show | 22 | HG01070.hp2 HG01071.hp1 HG01192.hp2 others(19): Show |
intron_variant | MODIFIER | c.-81+7374G>C | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 1/7 | chr8 | 65652158 | ||||||
| chr8:65652362
|
G | A | 65 | a0001c0001t0002g0001a0001c0001t0002g0039a0001c0001t0002g0042others(62): Show | 66 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(63): Show |
intron_variant | MODIFIER | c.-81+7578G>A | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 1/7 | chr8 | 65652362 | ||||||
| chr8:65652532
|
C | A | 1 | a0001c0001t0001g0305 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.-81+7748C>A | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 1/7 | chr8 | 65652532 | ||||||
| chr8:65652564
|
A | G | 1 | a0001c0001t0001g0233 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.-81+7780A>G | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 1/7 | chr8 | 65652564 | ||||||
| chr8:65652660
|
G | T | 1 | a0001c0001t0001g0291 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.-81+7876G>T | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 1/7 | chr8 | 65652660 | ||||||
| chr8:65652891
|
A | C | 1 | a0001c0001t0001g0178 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.-81+8107A>C | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 1/7 | chr8 | 65652891 | ||||||
| chr8:65652937
|
C | T | 65 | a0001c0001t0002g0001a0001c0001t0002g0039a0001c0001t0002g0042others(62): Show | 66 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(63): Show |
intron_variant | MODIFIER | c.-81+8153C>T | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 1/7 | chr8 | 65652937 | ||||||
| chr8:65653123
|
T | C | 10 | a0001c0001t0001g0293a0001c0001t0001g0294a0001c0001t0001g0295others(7): Show | 10 | HG01070.hp2 HG01071.hp1 HG02258.hp1 others(7): Show |
intron_variant | MODIFIER | c.-81+8339T>C | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 1/7 | chr8 | 65653123 | ||||||
| chr8:65653168
|
G | A | 256 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0006others(253): Show | 259 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(256): Show |
intron_variant | MODIFIER | c.-81+8384G>A | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 1/7 | chr8 | 65653168 | ||||||
| chr8:65653229
|
T | C | 65 | a0001c0001t0002g0001a0001c0001t0002g0039a0001c0001t0002g0042others(62): Show | 66 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(63): Show |
intron_variant | MODIFIER | c.-81+8445T>C | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 1/7 | chr8 | 65653229 | ||||||
| chr8:65653230
|
C | T | 65 | a0001c0001t0002g0001a0001c0001t0002g0039a0001c0001t0002g0042others(62): Show | 66 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(63): Show |
intron_variant | MODIFIER | c.-81+8446C>T | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 1/7 | chr8 | 65653230 | ||||||
| chr8:65653233
|
G | T | 65 | a0001c0001t0002g0001a0001c0001t0002g0039a0001c0001t0002g0042others(62): Show | 66 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(63): Show |
intron_variant | MODIFIER | c.-81+8449G>T | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 1/7 | chr8 | 65653233 | ||||||
| chr8:65653234
|
C | G | 1 | a0001c0001t0001g0100 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.-81+8450C>G | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 1/7 | chr8 | 65653234 | ||||||
| chr8:65653266
|
T | C | 32 | a0001c0001t0002g0001a0001c0001t0002g0039a0001c0001t0002g0042others(29): Show | 33 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(30): Show |
intron_variant | MODIFIER | c.-81+8482T>C | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 1/7 | chr8 | 65653266 | ||||||
| chr8:65653327
|
T | C | 252 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0006others(249): Show | 255 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(252): Show |
intron_variant | MODIFIER | c.-81+8543T>C | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 1/7 | chr8 | 65653327 | ||||||
| chr8:65653404
|
C | T | 2 | a0001c0001t0004g0081a0001c0001t0004g0082 | 2 | NA18939.hp2 NA19011.hp1 |
intron_variant | MODIFIER | c.-81+8620C>T | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 1/7 | chr8 | 65653404 | ||||||
| chr8:65653957
|
G | A | 9 | a0001c0001t0005g0014a0001c0001t0005g0015a0001c0001t0005g0018others(6): Show | 9 | HG02486.hp1 HG02647.hp2 HG02965.hp1 others(6): Show |
intron_variant | MODIFIER | c.-81+9173G>A | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 1/7 | chr8 | 65653957 | ||||||
| chr8:65653988
|
G | A | 3 | a0001c0001t0006g0340a0001c0001t0006g0341a0001c0001t0006g0342 | 3 | HG00733.hp1 HG01074.hp1 HG04204.hp1 |
intron_variant | MODIFIER | c.-81+9204G>A | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 1/7 | chr8 | 65653988 | ||||||
| chr8:65654064
|
C | CA | 44 | a0001c0001t0001g0094a0001c0001t0001g0100a0001c0001t0001g0239others(41): Show | 45 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(42): Show |
intron_variant | MODIFIER | c.-81+9298dupA | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr8 | 65654064 | |||||
| chr8:65654064
|
CA | C | 73 | a0001c0001t0001g0074a0001c0001t0001g0075a0001c0001t0001g0079others(70): Show | 73 | HG00408.hp2 HG00438.hp1 HG00438.hp2 others(70): Show |
intron_variant | MODIFIER | c.-81+9298delA | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr8 | 65654064 | |||||
| chr8:65654153
|
T | C | 1 | a0001c0001t0001g0145 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.-81+9369T>C | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 1/7 | chr8 | 65654153 | ||||||
| chr8:65654186
|
C | T | 71 | a0001c0001t0001g0074a0001c0001t0001g0075a0001c0001t0001g0079others(68): Show | 71 | HG00408.hp2 HG00438.hp1 HG00438.hp2 others(68): Show |
intron_variant | MODIFIER | c.-81+9402C>T | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 1/7 | chr8 | 65654186 | ||||||
| chr8:65654255
|
T | G | 65 | a0001c0001t0002g0001a0001c0001t0002g0039a0001c0001t0002g0042others(62): Show | 66 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(63): Show |
intron_variant | MODIFIER | c.-81+9471T>G | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 1/7 | chr8 | 65654255 | ||||||
| chr8:65654303
|
A | G | 65 | a0001c0001t0002g0001a0001c0001t0002g0039a0001c0001t0002g0042others(62): Show | 66 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(63): Show |
intron_variant | MODIFIER | c.-81+9519A>G | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 1/7 | chr8 | 65654303 | ||||||
| chr8:65654397
|
C | T | 12 | a0001c0001t0001g0002a0001c0001t0001g0094a0001c0001t0001g0095others(9): Show | 13 | HG02027.hp1 NA18944.hp2 NA18957.hp2 others(10): Show |
intron_variant | MODIFIER | c.-81+9613C>T | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 1/7 | chr8 | 65654397 | ||||||
| chr8:65654478
|
T | C | 21 | a0001c0001t0003g0016a0001c0001t0003g0022a0001c0001t0003g0023others(18): Show | 21 | HG00140.hp1 HG00642.hp2 HG01168.hp2 others(18): Show |
intron_variant | MODIFIER | c.-81+9694T>C | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 1/7 | chr8 | 65654478 | ||||||
| chr8:65654580
|
G | GTGTGT | 65 | a0001c0001t0002g0001a0001c0001t0002g0039a0001c0001t0002g0042others(62): Show | 66 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(63): Show |
intron_variant | MODIFIER | c.-81+9808_-81+9812d others(7): Show |
MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr8 | 65654580 | |||||
| chr8:65654581
|
T | A | 12 | a0001c0001t0001g0002a0001c0001t0001g0094a0001c0001t0001g0095others(9): Show | 13 | HG02027.hp1 NA18944.hp2 NA18957.hp2 others(10): Show |
intron_variant | MODIFIER | c.-81+9797T>A | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 1/7 | chr8 | 65654581 | ||||||
| chr8:65655027
|
C | T | 2 | a0001c0001t0001g0223a0001c0001t0001g0261 | 2 | HG01168.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.-81+10243C>T | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 1/7 | chr8 | 65655027 | ||||||
| chr8:65655148
|
C | G | 14 | a0001c0001t0001g0142a0001c0001t0001g0207a0001c0001t0001g0216others(11): Show | 14 | HG02080.hp1 NA18955.hp1 NA18959.hp2 others(11): Show |
intron_variant | MODIFIER | c.-81+10364C>G | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 1/7 | chr8 | 65655148 | ||||||
| chr8:65655341
|
A | G | 21 | a0001c0001t0003g0016a0001c0001t0003g0022a0001c0001t0003g0023others(18): Show | 21 | HG00140.hp1 HG00642.hp2 HG01168.hp2 others(18): Show |
intron_variant | MODIFIER | c.-81+10557A>G | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 1/7 | chr8 | 65655341 | ||||||
| chr8:65655413
|
T | C | 1 | a0001c0001t0001g0332 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.-81+10629T>C | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 1/7 | chr8 | 65655413 | ||||||
| chr8:65655418
|
G | T | 3 | a0001c0001t0001g0222a0001c0001t0001g0255a0001c0001t0001g0256 | 3 | HG02145.hp2 HG02647.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.-81+10634G>T | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 1/7 | chr8 | 65655418 | ||||||
| chr8:65655581
|
A | T | 2 | a0001c0001t0001g0257a0001c0001t0001g0258 | 2 | HG01243.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.-81+10797A>T | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 1/7 | chr8 | 65655581 | ||||||
| chr8:65655596
|
G | A | 255 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0006others(252): Show | 258 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(255): Show |
intron_variant | MODIFIER | c.-81+10812G>A | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 1/7 | chr8 | 65655596 | ||||||
| chr8:65655598
|
A | G | 1 | a0001c0001t0001g0330 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.-81+10814A>G | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 1/7 | chr8 | 65655598 | ||||||
| chr8:65655820
|
G | A | 1 | a0001c0001t0007g0106 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.-81+11036G>A | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 1/7 | chr8 | 65655820 | ||||||
| chr8:65655949
|
A | ATATATAT others(6): Show |
3 | a0001c0001t0001g0080a0001c0001t0001g0203a0001c0001t0004g0202 | 3 | HG02735.hp1 NA18950.hp1 NA19058.hp2 |
intron_variant | MODIFIER | c.-81+11165_-81+1116 others(17): Show |
MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 1/7 | chr8 | 65655949 | ||||||
| chr8:65655951
|
A | ATATATAT others(6): Show |
48 | a0001c0001t0001g0074a0001c0001t0001g0075a0001c0001t0001g0079others(45): Show | 48 | HG00408.hp2 HG00438.hp1 HG00438.hp2 others(45): Show |
intron_variant | MODIFIER | c.-81+11167_-81+1116 others(17): Show |
MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 1/7 | chr8 | 65655951 | ||||||
| chr8:65655951
|
A | ATATATAT others(10): Show |
11 | a0001c0001t0001g0102a0001c0001t0001g0105a0001c0001t0001g0109others(8): Show | 11 | HG00621.hp1 HG00621.hp2 HG02027.hp2 others(8): Show |
intron_variant | MODIFIER | c.-81+11167_-81+1116 others(21): Show |
MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 1/7 | chr8 | 65655951 | ||||||
| chr8:65655951
|
A | ATATATAT others(14): Show |
1 | a0001c0001t0001g0278 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.-81+11167_-81+1116 others(25): Show |
MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 1/7 | chr8 | 65655951 | ||||||
| chr8:65655951
|
A | ATATATAT others(42): Show |
2 | a0001c0001t0001g0200a0001c0001t0001g0285 | 2 | HG03491.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.-81+11167_-81+1116 others(53): Show |
MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 1/7 | chr8 | 65655951 | ||||||
| chr8:65655951
|
A | ATATATAT others(40): Show |
1 | a0001c0001t0001g0201 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.-81+11167_-81+1116 others(51): Show |
MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 1/7 | chr8 | 65655951 | ||||||
| chr8:65655951
|
A | ATATATAT others(30): Show |
1 | a0001c0001t0004g0137 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.-81+11167_-81+1116 others(41): Show |
MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 1/7 | chr8 | 65655951 | ||||||
| chr8:65655951
|
A | T | 58 | a0001c0001t0001g0005a0001c0001t0001g0080a0001c0001t0001g0183others(55): Show | 59 | HG00099.hp2 HG00323.hp2 HG00639.hp1 others(56): Show |
intron_variant | MODIFIER | c.-81+11167A>T | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 1/7 | chr8 | 65655951 | ||||||
| chr8:65655951
|
AATATATA others(14): Show |
A | 6 | a0001c0001t0002g0043a0001c0001t0002g0047a0001c0001t0002g0048others(3): Show | 6 | HG00735.hp1 HG00741.hp1 HG01192.hp1 others(3): Show |
intron_variant | MODIFIER | c.-81+11180_-81+1120 others(25): Show |
MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr8 | 65655951 | |||||
| chr8:65655952
|
A | AATATATA others(8): Show |
2 | a0001c0001t0001g0107a0001c0001t0004g0139 | 2 | HG01106.hp2 NA18979.hp2 |
intron_variant | MODIFIER | c.-81+11168_-81+1116 others(19): Show |
MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 1/7 | chr8 | 65655952 | ||||||
| chr8:65655952
|
ATATATAT others(2): Show |
A | 3 | a0001c0001t0008g0011a0001c0001t0008g0012a0001c0001t0008g0013 | 3 | HG02486.hp1 HG03130.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.-81+11169_-81+1117 others(13): Show |
MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 1/7 | chr8 | 65655952 | ||||||
| chr8:65655953
|
T | A | 45 | a0001c0001t0001g0071a0001c0001t0001g0072a0001c0001t0001g0073others(42): Show | 45 | HG00140.hp1 HG00642.hp2 HG01069.hp1 others(42): Show |
intron_variant | MODIFIER | c.-81+11169T>A | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 1/7 | chr8 | 65655953 | ||||||
| chr8:65655954
|
A | G | 51 | a0001c0001t0001g0074a0001c0001t0001g0075a0001c0001t0001g0079others(48): Show | 51 | HG00408.hp2 HG00438.hp1 HG00438.hp2 others(48): Show |
intron_variant | MODIFIER | c.-81+11170A>G | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 1/7 | chr8 | 65655954 | ||||||
| chr8:65655955
|
T | A | 12 | a0001c0001t0003g0024a0001c0001t0003g0025a0001c0001t0003g0026others(9): Show | 12 | HG02647.hp2 HG02965.hp1 HG03540.hp1 others(9): Show |
intron_variant | MODIFIER | c.-81+11171T>A | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 1/7 | chr8 | 65655955 | ||||||
| chr8:65655959
|
TATATATA others(4): Show |
T | 51 | a0001c0001t0002g0001a0001c0001t0002g0039a0001c0001t0002g0042others(48): Show | 52 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(49): Show |
intron_variant | MODIFIER | c.-81+11185_-81+1119 others(15): Show |
MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr8 | 65655959 | |||||
| chr8:65655961
|
TATATATA others(2): Show |
T | 4 | a0001c0001t0005g0014a0001c0001t0006g0340a0001c0001t0006g0341others(1): Show | 4 | HG00733.hp1 HG01074.hp1 HG02647.hp2 others(1): Show |
intron_variant | MODIFIER | c.-81+11185_-81+1119 others(13): Show |
MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr8 | 65655961 | |||||
| chr8:65655963
|
T | A | 3 | a0001c0001t0008g0011a0001c0001t0008g0012a0001c0001t0008g0013 | 3 | HG02486.hp1 HG03130.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.-81+11179T>A | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 1/7 | chr8 | 65655963 | ||||||
| chr8:65655965
|
T | A | 3 | a0001c0001t0008g0011a0001c0001t0008g0012a0001c0001t0008g0013 | 3 | HG02486.hp1 HG03130.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.-81+11181T>A | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 1/7 | chr8 | 65655965 | ||||||
| chr8:65655966
|
A | G | 2 | a0001c0001t0001g0108a0001c0001t0001g0277 | 2 | HG04115.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.-81+11182A>G | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 1/7 | chr8 | 65655966 | ||||||
| chr8:65655967
|
T | C | 1 | a0001c0001t0001g0229 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.-81+11183T>C | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 1/7 | chr8 | 65655967 | ||||||
| chr8:65655967
|
TACC | T | 8 | a0001c0001t0001g0200a0001c0001t0001g0201a0001c0001t0001g0285others(5): Show | 8 | HG01934.hp1 HG02486.hp1 HG03130.hp2 others(5): Show |
intron_variant | MODIFIER | c.-81+11185_-81+1118 others(7): Show |
MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr8 | 65655967 | |||||
| chr8:65655968
|
A | AT | 53 | a0001c0001t0001g0074a0001c0001t0001g0075a0001c0001t0001g0079others(50): Show | 53 | HG00408.hp2 HG00438.hp1 HG00438.hp2 others(50): Show |
intron_variant | MODIFIER | c.-81+11184_-81+1118 others(5): Show |
MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 1/7 | chr8 | 65655968 | ||||||
| chr8:65655968
|
A | ATACATAT others(48): Show |
1 | a0001c0001t0001g0322 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.-81+11184_-81+1118 others(59): Show |
MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 1/7 | chr8 | 65655968 | ||||||
| chr8:65655968
|
A | ATACATAT others(6): Show |
1 | a0001c0001t0001g0250 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.-81+11184_-81+1118 others(17): Show |
MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 1/7 | chr8 | 65655968 | ||||||
| chr8:65655968
|
A | ATACATAT others(58): Show |
2 | a0001c0001t0001g0294a0001c0001t0001g0302 | 2 | HG02258.hp1 HG02717.hp1 |
intron_variant | MODIFIER | c.-81+11184_-81+1118 others(69): Show |
MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 1/7 | chr8 | 65655968 | ||||||
| chr8:65655968
|
A | ATACATAT others(56): Show |
4 | a0001c0001t0001g0293a0001c0001t0001g0295a0001c0001t0001g0296others(1): Show | 4 | HG01070.hp2 HG01071.hp1 HG02280.hp2 others(1): Show |
intron_variant | MODIFIER | c.-81+11184_-81+1118 others(67): Show |
MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 1/7 | chr8 | 65655968 | ||||||
| chr8:65655968
|
A | ATACATAT others(56): Show |
1 | a0001c0001t0001g0298 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.-81+11184_-81+1118 others(67): Show |
MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 1/7 | chr8 | 65655968 | ||||||
| chr8:65655968
|
A | ATACATAT others(54): Show |
2 | a0001c0001t0001g0299a0001c0001t0001g0300 | 2 | HG03098.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.-81+11184_-81+1118 others(65): Show |
MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 1/7 | chr8 | 65655968 | ||||||
| chr8:65655968
|
A | ATACATAT others(54): Show |
1 | a0001c0001t0001g0301 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.-81+11184_-81+1118 others(65): Show |
MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 1/7 | chr8 | 65655968 | ||||||
| chr8:65655968
|
A | ATATATAT others(6): Show |
2 | a0001c0001t0001g0108a0001c0001t0001g0277 | 2 | HG04115.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.-81+11184_-81+1118 others(17): Show |
MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 1/7 | chr8 | 65655968 | ||||||
| chr8:65655968
|
A | ATATATAT others(42): Show |
1 | a0001c0001t0001g0229 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.-81+11184_-81+1118 others(53): Show |
MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 1/7 | chr8 | 65655968 | ||||||
| chr8:65655968
|
A | ATATATAT others(34): Show |
1 | a0001c0001t0001g0273 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.-81+11184_-81+1118 others(45): Show |
MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 1/7 | chr8 | 65655968 | ||||||
| chr8:65655968
|
A | ATGTATAT others(26): Show |
1 | a0001c0001t0001g0101 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.-81+11184_-81+1118 others(37): Show |
MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 1/7 | chr8 | 65655968 | ||||||
| chr8:65655968
|
AC | A | 12 | a0001c0001t0001g0105a0001c0001t0001g0107a0001c0001t0001g0110others(9): Show | 12 | HG00621.hp2 HG01106.hp2 HG02027.hp2 others(9): Show |
intron_variant | MODIFIER | c.-81+11186delC | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr8 | 65655968 | |||||
| chr8:65655969
|
C | A | 70 | a0001c0001t0001g0074a0001c0001t0001g0075a0001c0001t0001g0079others(67): Show | 70 | HG00408.hp2 HG00438.hp1 HG00438.hp2 others(67): Show |
intron_variant | MODIFIER | c.-81+11185C>A | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 1/7 | chr8 | 65655969 | ||||||
| chr8:65655969
|
C | CACATATA others(48): Show |
1 | a0001c0001t0001g0141 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.-81+11185_-81+1118 others(59): Show |
MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 1/7 | chr8 | 65655969 | ||||||
| chr8:65655969
|
C | CATATATA others(26): Show |
1 | a0001c0001t0001g0333 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.-81+11185_-81+1118 others(37): Show |
MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 1/7 | chr8 | 65655969 | ||||||
| chr8:65655969
|
C | CATATATA others(28): Show |
1 | a0001c0001t0001g0312 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.-81+11185_-81+1118 others(39): Show |
MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 1/7 | chr8 | 65655969 | ||||||
| chr8:65655969
|
C | CATATATA others(46): Show |
33 | a0001c0001t0001g0005a0001c0001t0001g0223a0001c0001t0001g0235others(30): Show | 34 | HG00639.hp1 HG00639.hp2 HG00735.hp2 others(31): Show |
intron_variant | MODIFIER | c.-81+11185_-81+1118 others(57): Show |
MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 1/7 | chr8 | 65655969 | ||||||
| chr8:65655969
|
C | CATATATA others(48): Show |
2 | a0001c0001t0001g0332a0001c0001t0001g0343 | 2 | HG00099.hp2 HG00323.hp2 |
intron_variant | MODIFIER | c.-81+11185_-81+1118 others(59): Show |
MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 1/7 | chr8 | 65655969 | ||||||
| chr8:65655969
|
C | CATATATA others(44): Show |
5 | a0001c0001t0001g0189a0001c0001t0001g0234a0001c0001t0001g0289others(2): Show | 5 | HG01243.hp1 HG02895.hp1 HG02896.hp2 others(2): Show |
intron_variant | MODIFIER | c.-81+11185_-81+1118 others(55): Show |
MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 1/7 | chr8 | 65655969 | ||||||
| chr8:65655969
|
C | CATATATA others(2): Show |
3 | a0001c0001t0001g0249a0001c0001t0001g0252a0001c0001t0001g0253 | 3 | HG02622.hp1 HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.-81+11185_-81+1118 others(13): Show |
MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 1/7 | chr8 | 65655969 | ||||||
| chr8:65655969
|
C | CATATATA others(4): Show |
5 | a0001c0001t0001g0251a0001c0001t0001g0254a0001c0001t0001g0262others(2): Show | 5 | HG01192.hp2 HG01884.hp2 HG01891.hp2 others(2): Show |
intron_variant | MODIFIER | c.-81+11185_-81+1118 others(15): Show |
MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 1/7 | chr8 | 65655969 | ||||||
| chr8:65655969
|
C | CATATATA others(8): Show |
2 | a0001c0001t0001g0255a0001c0001t0001g0256 | 2 | HG02145.hp2 HG02647.hp1 |
intron_variant | MODIFIER | c.-81+11185_-81+1118 others(19): Show |
MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 1/7 | chr8 | 65655969 | ||||||
| chr8:65655969
|
C | CATATATA others(10): Show |
1 | a0001c0001t0001g0222 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.-81+11185_-81+1118 others(21): Show |
MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 1/7 | chr8 | 65655969 | ||||||
| chr8:65655969
|
C | CATATATA others(20): Show |
1 | a0001c0001t0001g0271 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.-81+11185_-81+1118 others(31): Show |
MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 1/7 | chr8 | 65655969 | ||||||
| chr8:65655969
|
C | CATATATA others(22): Show |
1 | a0001c0001t0001g0272 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.-81+11185_-81+1118 others(33): Show |
MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 1/7 | chr8 | 65655969 | ||||||
| chr8:65655969
|
C | CATATATA others(32): Show |
1 | a0001c0001t0001g0258 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.-81+11185_-81+1118 others(43): Show |
MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 1/7 | chr8 | 65655969 | ||||||
| chr8:65655969
|
C | CATATATA others(34): Show |
2 | a0001c0001t0001g0238a0001c0001t0001g0257 | 2 | HG01243.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.-81+11185_-81+1118 others(45): Show |
MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 1/7 | chr8 | 65655969 | ||||||
| chr8:65655969
|
C | CATATATA others(48): Show |
1 | a0001c0001t0001g0305 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.-81+11185_-81+1118 others(59): Show |
MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 1/7 | chr8 | 65655969 | ||||||
| chr8:65655969
|
C | CATATATA others(44): Show |
1 | a0001c0001t0001g0230 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.-81+11185_-81+1118 others(55): Show |
MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 1/7 | chr8 | 65655969 | ||||||
| chr8:65655969
|
C | CATATATA others(44): Show |
1 | a0001c0001t0001g0306 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.-81+11185_-81+1118 others(55): Show |
MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 1/7 | chr8 | 65655969 | ||||||
| chr8:65655969
|
C | CATATATA others(46): Show |
3 | a0001c0001t0001g0307a0001c0001t0001g0308a0001c0001t0001g0309 | 3 | HG01891.hp1 HG02809.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.-81+11185_-81+1118 others(57): Show |
MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 1/7 | chr8 | 65655969 | ||||||
| chr8:65655969
|
C | CATATATA others(66): Show |
1 | a0001c0001t0001g0264 | 1 | HG02897.hp1 | intron_variant | MODIFIER | c.-81+11185_-81+1118 others(77): Show |
MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 1/7 | chr8 | 65655969 | ||||||
| chr8:65655969
|
C | CATATATA others(68): Show |
1 | a0001c0001t0001g0263 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.-81+11185_-81+1118 others(79): Show |
MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 1/7 | chr8 | 65655969 | ||||||
| chr8:65655969
|
C | CATATATA others(48): Show |
2 | a0001c0001t0001g0010a0001c0001t0001g0183 | 2 | HG03486.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.-81+11185_-81+1118 others(59): Show |
MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 1/7 | chr8 | 65655969 | ||||||
| chr8:65655969
|
C | CATATATA others(50): Show |
3 | a0001c0001t0001g0006a0001c0001t0001g0009a0001c0001t0001g0226 | 3 | HG02055.hp1 HG02970.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.-81+11185_-81+1118 others(61): Show |
MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 1/7 | chr8 | 65655969 | ||||||
| chr8:65655969
|
C | CATATATA others(52): Show |
1 | a0001c0001t0001g0268 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.-81+11185_-81+1118 others(63): Show |
MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 1/7 | chr8 | 65655969 | ||||||
| chr8:65655969
|
C | CATATATA others(58): Show |
1 | a0001c0001t0001g0008 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.-81+11185_-81+1118 others(69): Show |
MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 1/7 | chr8 | 65655969 | ||||||
| chr8:65655969
|
C | CATATATA others(60): Show |
1 | a0001c0001t0001g0265 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.-81+11185_-81+1118 others(71): Show |
MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 1/7 | chr8 | 65655969 | ||||||
| chr8:65655969
|
C | CATATATA others(62): Show |
1 | a0001c0001t0001g0007 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.-81+11185_-81+1118 others(73): Show |
MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 1/7 | chr8 | 65655969 | ||||||
| chr8:65655969
|
C | CATATATA others(66): Show |
1 | a0001c0001t0001g0267 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.-81+11185_-81+1118 others(77): Show |
MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 1/7 | chr8 | 65655969 | ||||||
| chr8:65655969
|
C | CATATATA others(76): Show |
1 | a0001c0001t0001g0225 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.-81+11185_-81+1118 others(87): Show |
MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 1/7 | chr8 | 65655969 | ||||||
| chr8:65655969
|
C | CATATATA others(54): Show |
1 | a0001c0001t0001g0224 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.-81+11185_-81+1118 others(65): Show |
MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 1/7 | chr8 | 65655969 | ||||||
| chr8:65655969
|
C | CATATATA others(28): Show |
4 | a0001c0001t0001g0071a0001c0001t0001g0072a0001c0001t0001g0073others(1): Show | 4 | HG02559.hp2 HG02622.hp2 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.-81+11185_-81+1118 others(39): Show |
MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 1/7 | chr8 | 65655969 | ||||||
| chr8:65655969
|
C | CATATATA others(30): Show |
1 | a0001c0001t0001g0286 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.-81+11185_-81+1118 others(41): Show |
MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 1/7 | chr8 | 65655969 | ||||||
| chr8:65655969
|
C | CATATATA others(34): Show |
1 | a0001c0001t0001g0287 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.-81+11185_-81+1118 others(45): Show |
MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 1/7 | chr8 | 65655969 | ||||||
| chr8:65655969
|
C | CATATATA others(46): Show |
1 | a0001c0001t0001g0274 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.-81+11185_-81+1118 others(57): Show |
MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 1/7 | chr8 | 65655969 | ||||||
| chr8:65655969
|
C | CATATATA others(48): Show |
1 | a0001c0001t0001g0270 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.-81+11185_-81+1118 others(59): Show |
MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 1/7 | chr8 | 65655969 | ||||||
| chr8:65655969
|
C | CATATATA others(62): Show |
1 | a0001c0001t0001g0339 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.-81+11185_-81+1118 others(73): Show |
MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 1/7 | chr8 | 65655969 | ||||||
| chr8:65655969
|
C | CATATATA others(42): Show |
1 | a0001c0001t0001g0266 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.-81+11185_-81+1118 others(53): Show |
MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 1/7 | chr8 | 65655969 | ||||||
| chr8:65655969
|
C | CATATATA others(50): Show |
1 | a0001c0001t0001g0310 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.-81+11185_-81+1118 others(61): Show |
MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 1/7 | chr8 | 65655969 | ||||||
| chr8:65655969
|
C | CATATATA others(54): Show |
1 | a0001c0001t0001g0227 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.-81+11185_-81+1118 others(65): Show |
MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 1/7 | chr8 | 65655969 | ||||||
| chr8:65655969
|
C | CATATATA others(44): Show |
1 | a0001c0001t0001g0099 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.-81+11185_-81+1118 others(55): Show |
MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 1/7 | chr8 | 65655969 | ||||||
| chr8:65655969
|
C | CATATATA others(46): Show |
8 | a0001c0001t0001g0002a0001c0001t0001g0094a0001c0001t0001g0095others(5): Show | 9 | NA18944.hp2 NA18957.hp2 NA18970.hp2 others(6): Show |
intron_variant | MODIFIER | c.-81+11185_-81+1118 others(57): Show |
MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 1/7 | chr8 | 65655969 | ||||||
| chr8:65655969
|
C | CATATATA others(46): Show |
1 | a0001c0001t0001g0100 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.-81+11185_-81+1118 others(57): Show |
MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 1/7 | chr8 | 65655969 | ||||||
| chr8:65655969
|
C | CATATATA others(36): Show |
3 | a0001c0001t0001g0085a0001c0001t0001g0086a0001c0001t0001g0087 | 3 | HG02257.hp2 HG03098.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.-81+11185_-81+1118 others(47): Show |
MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 1/7 | chr8 | 65655969 | ||||||
| chr8:65655969
|
C | CATATATA others(54): Show |
1 | a0001c0001t0001g0228 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.-81+11185_-81+1118 others(65): Show |
MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 1/7 | chr8 | 65655969 | ||||||
| chr8:65655970
|
C | T | 187 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0006others(184): Show | 189 | HG00099.hp2 HG00323.hp2 HG00408.hp2 others(186): Show |
intron_variant | MODIFIER | c.-81+11186C>T | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 1/7 | chr8 | 65655970 | ||||||
| chr8:65655986
|
G | A | 65 | a0001c0001t0002g0001a0001c0001t0002g0039a0001c0001t0002g0042others(62): Show | 66 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(63): Show |
intron_variant | MODIFIER | c.-81+11202G>A | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 1/7 | chr8 | 65655986 | ||||||
| chr8:65656095
|
C | T | 65 | a0001c0001t0002g0001a0001c0001t0002g0039a0001c0001t0002g0042others(62): Show | 66 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(63): Show |
intron_variant | MODIFIER | c.-81+11311C>T | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 1/7 | chr8 | 65656095 | ||||||
| chr8:65656151
|
A | C | 1 | a0001c0001t0001g0250 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.-81+11367A>C | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 1/7 | chr8 | 65656151 | ||||||
| chr8:65656187
|
ACT | A | 30 | a0001c0001t0002g0001a0001c0001t0002g0039a0001c0001t0002g0042others(27): Show | 31 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(28): Show |
intron_variant | MODIFIER | c.-81+11406_-81+1140 others(6): Show |
MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr8 | 65656187 | |||||
| chr8:65656199
|
A | AAAAAC | 11 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008others(8): Show | 11 | HG01255.hp2 HG01433.hp2 HG01891.hp1 others(8): Show |
intron_variant | MODIFIER | c.-81+11430_-81+1143 others(9): Show |
MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr8 | 65656199 | |||||
| chr8:65656266
|
G | A | 65 | a0001c0001t0002g0001a0001c0001t0002g0039a0001c0001t0002g0042others(62): Show | 66 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(63): Show |
intron_variant | MODIFIER | c.-81+11482G>A | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 1/7 | chr8 | 65656266 | ||||||
| chr8:65656382
|
T | G | 255 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0006others(252): Show | 258 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(255): Show |
intron_variant | MODIFIER | c.-81+11598T>G | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 1/7 | chr8 | 65656382 | ||||||
| chr8:65656469
|
G | T | 22 | a0001c0001t0001g0222a0001c0001t0001g0249a0001c0001t0001g0250others(19): Show | 22 | HG01070.hp2 HG01071.hp1 HG01192.hp2 others(19): Show |
intron_variant | MODIFIER | c.-81+11685G>T | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 1/7 | chr8 | 65656469 | ||||||
| chr8:65656500
|
A | AT | 13 | a0001c0001t0001g0009a0001c0001t0001g0093a0001c0001t0001g0138others(10): Show | 13 | HG01169.hp2 HG01934.hp2 HG02055.hp1 others(10): Show |
intron_variant | MODIFIER | c.-81+11735dupT | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr8 | 65656500 | |||||
| chr8:65656540
|
T | C | 65 | a0001c0001t0002g0001a0001c0001t0002g0039a0001c0001t0002g0042others(62): Show | 66 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(63): Show |
intron_variant | MODIFIER | c.-81+11756T>C | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 1/7 | chr8 | 65656540 | ||||||
| chr8:65657017
|
A | AT | 8 | a0001c0001t0001g0189a0001c0001t0001g0234a0001c0001t0001g0235others(5): Show | 8 | HG01243.hp1 HG01884.hp1 HG02559.hp1 others(5): Show |
intron_variant | MODIFIER | c.-81+12246dupT | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr8 | 65657017 | |||||
| chr8:65657020
|
T | A | 1 | a0001c0001t0001g0230 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.-81+12236T>A | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 1/7 | chr8 | 65657020 | ||||||
| chr8:65657035
|
C | T | 2 | a0001c0001t0001g0173a0001c0001t0001g0174 | 2 | HG01069.hp2 HG01071.hp2 |
intron_variant | MODIFIER | c.-81+12251C>T | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 1/7 | chr8 | 65657035 | ||||||
| chr8:65657122
|
T | C | 32 | a0001c0001t0002g0001a0001c0001t0002g0039a0001c0001t0002g0042others(29): Show | 33 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(30): Show |
intron_variant | MODIFIER | c.-81+12338T>C | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 1/7 | chr8 | 65657122 | ||||||
| chr8:65657155
|
A | G | 1 | a0001c0001t0001g0238 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.-81+12371A>G | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 1/7 | chr8 | 65657155 | ||||||
| chr8:65657249
|
G | A | 1 | a0001c0001t0001g0339 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.-81+12465G>A | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 1/7 | chr8 | 65657249 | ||||||
| chr8:65657331
|
A | C | 65 | a0001c0001t0002g0001a0001c0001t0002g0039a0001c0001t0002g0042others(62): Show | 66 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(63): Show |
intron_variant | MODIFIER | c.-80-12542A>C | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 1/7 | chr8 | 65657331 | ||||||
| chr8:65657357
|
G | A | 1 | a0001c0001t0001g0233 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.-80-12516G>A | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 1/7 | chr8 | 65657357 | ||||||
| chr8:65657358
|
T | A | 1 | a0001c0001t0001g0233 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.-80-12515T>A | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 1/7 | chr8 | 65657358 | ||||||
| chr8:65657359
|
T | A | 1 | a0001c0001t0001g0233 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.-80-12514T>A | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 1/7 | chr8 | 65657359 | ||||||
| chr8:65657360
|
T | C | 1 | a0001c0001t0001g0233 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.-80-12513T>C | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 1/7 | chr8 | 65657360 | ||||||
| chr8:65657361
|
T | A | 1 | a0001c0001t0001g0233 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.-80-12512T>A | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 1/7 | chr8 | 65657361 | ||||||
| chr8:65657362
|
T | A | 1 | a0001c0001t0001g0233 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.-80-12511T>A | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 1/7 | chr8 | 65657362 | ||||||
| chr8:65657363
|
G | A | 1 | a0001c0001t0001g0233 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.-80-12510G>A | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 1/7 | chr8 | 65657363 | ||||||
| chr8:65657364
|
T | A | 1 | a0001c0001t0001g0233 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.-80-12509T>A | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 1/7 | chr8 | 65657364 | ||||||
| chr8:65657365
|
T | A | 1 | a0001c0001t0001g0233 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.-80-12508T>A | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 1/7 | chr8 | 65657365 | ||||||
| chr8:65657366
|
G | A | 1 | a0001c0001t0001g0233 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.-80-12507G>A | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 1/7 | chr8 | 65657366 | ||||||
| chr8:65657367
|
T | C | 1 | a0001c0001t0001g0233 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.-80-12506T>C | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 1/7 | chr8 | 65657367 | ||||||
| chr8:65657370
|
T | C | 1 | a0001c0001t0001g0233 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.-80-12503T>C | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 1/7 | chr8 | 65657370 | ||||||
| chr8:65657371
|
T | C | 1 | a0001c0001t0001g0233 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.-80-12502T>C | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 1/7 | chr8 | 65657371 | ||||||
| chr8:65657375
|
G | C | 1 | a0001c0001t0001g0233 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.-80-12498G>C | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 1/7 | chr8 | 65657375 | ||||||
| chr8:65657386
|
C | T | 1 | a0001c0001t0001g0233 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.-80-12487C>T | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 1/7 | chr8 | 65657386 | ||||||
| chr8:65657389
|
T | A | 1 | a0001c0001t0001g0233 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.-80-12484T>A | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 1/7 | chr8 | 65657389 | ||||||
| chr8:65657404
|
A | C | 1 | a0001c0001t0001g0233 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.-80-12469A>C | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 1/7 | chr8 | 65657404 | ||||||
| chr8:65657405
|
G | T | 1 | a0001c0001t0001g0233 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.-80-12468G>T | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 1/7 | chr8 | 65657405 | ||||||
| chr8:65657407
|
G | T | 1 | a0001c0001t0001g0233 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.-80-12466G>T | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 1/7 | chr8 | 65657407 | ||||||
| chr8:65657462
|
G | A | 1 | a0001c0001t0007g0106 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.-80-12411G>A | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 1/7 | chr8 | 65657462 | ||||||
| chr8:65657496
|
A | C | 62 | a0001c0001t0002g0001a0001c0001t0002g0039a0001c0001t0002g0042others(59): Show | 63 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(60): Show |
intron_variant | MODIFIER | c.-80-12377A>C | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 1/7 | chr8 | 65657496 | ||||||
| chr8:65657515
|
C | T | 2 | a0001c0001t0002g0001a0001c0001t0002g0046 | 3 | HG01109.hp2 HG02280.hp1 NA20752.hp2 |
intron_variant | MODIFIER | c.-80-12358C>T | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 1/7 | chr8 | 65657515 | ||||||
| chr8:65657606
|
A | G | 1 | a0001c0001t0001g0199 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.-80-12267A>G | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 1/7 | chr8 | 65657606 | ||||||
| chr8:65657609
|
C | T | 5 | a0001c0001t0001g0260a0001c0001t0001g0322a0001c0001t0001g0329others(2): Show | 5 | HG00738.hp2 HG01070.hp1 HG01258.hp1 others(2): Show |
intron_variant | MODIFIER | c.-80-12264C>T | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 1/7 | chr8 | 65657609 | ||||||
| chr8:65657706
|
T | TA | 8 | a0001c0001t0001g0093a0001c0001t0001g0096a0001c0001t0001g0184others(5): Show | 8 | HG02602.hp2 HG02622.hp1 HG03471.hp1 others(5): Show |
intron_variant | MODIFIER | c.-80-12152dupA | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr8 | 65657706 | |||||
| chr8:65657706
|
TA | T | 8 | a0001c0001t0001g0085a0001c0001t0001g0086a0001c0001t0001g0087others(5): Show | 8 | HG00733.hp1 HG01074.hp1 HG02257.hp2 others(5): Show |
intron_variant | MODIFIER | c.-80-12152delA | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr8 | 65657706 | |||||
| chr8:65658095
|
ATCT | A | 21 | a0001c0001t0003g0016a0001c0001t0003g0022a0001c0001t0003g0023others(18): Show | 21 | HG00140.hp1 HG00642.hp2 HG01168.hp2 others(18): Show |
intron_variant | MODIFIER | c.-80-11773_-80-1177 others(7): Show |
MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr8 | 65658095 | |||||
| chr8:65658132
|
C | T | 65 | a0001c0001t0002g0001a0001c0001t0002g0039a0001c0001t0002g0042others(62): Show | 66 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(63): Show |
intron_variant | MODIFIER | c.-80-11741C>T | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 1/7 | chr8 | 65658132 | ||||||
| chr8:65658153
|
T | C | 1 | a0001c0001t0001g0230 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.-80-11720T>C | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 1/7 | chr8 | 65658153 | ||||||
| chr8:65658473
|
G | A | 65 | a0001c0001t0002g0001a0001c0001t0002g0039a0001c0001t0002g0042others(62): Show | 66 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(63): Show |
intron_variant | MODIFIER | c.-80-11400G>A | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 1/7 | chr8 | 65658473 | ||||||
| chr8:65658482
|
T | C | 1 | a0001c0001t0001g0240 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.-80-11391T>C | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 1/7 | chr8 | 65658482 | ||||||
| chr8:65658690
|
A | T | 1 | a0001c0001t0001g0284 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.-80-11183A>T | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 1/7 | chr8 | 65658690 | ||||||
| chr8:65658695
|
T | C | 65 | a0001c0001t0002g0001a0001c0001t0002g0039a0001c0001t0002g0042others(62): Show | 66 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(63): Show |
intron_variant | MODIFIER | c.-80-11178T>C | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 1/7 | chr8 | 65658695 | ||||||
| chr8:65658735
|
A | G | 6 | a0001c0001t0005g0014a0001c0001t0005g0015a0001c0001t0005g0018others(3): Show | 6 | HG02647.hp2 HG02965.hp1 HG03540.hp1 others(3): Show |
intron_variant | MODIFIER | c.-80-11138A>G | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 1/7 | chr8 | 65658735 | ||||||
| chr8:65658800
|
G | C | 1 | a0001c0001t0001g0230 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.-80-11073G>C | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 1/7 | chr8 | 65658800 | ||||||
| chr8:65658912
|
A | G | 1 | a0001c0001t0002g0064 | 1 | NA19080.hp2 | intron_variant | MODIFIER | c.-80-10961A>G | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 1/7 | chr8 | 65658912 | ||||||
| chr8:65659022
|
A | G | 2 | a0001c0001t0008g0011a0001c0001t0008g0012 | 2 | HG03130.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.-80-10851A>G | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 1/7 | chr8 | 65659022 | ||||||
| chr8:65659041
|
G | A | 1 | a0001c0001t0002g0042 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.-80-10832G>A | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 1/7 | chr8 | 65659041 | ||||||
| chr8:65659045
|
A | G | 1 | a0001c0001t0001g0145 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.-80-10828A>G | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 1/7 | chr8 | 65659045 | ||||||
| chr8:65659083
|
G | A | 3 | a0001c0001t0006g0340a0001c0001t0006g0341a0001c0001t0006g0342 | 3 | HG00733.hp1 HG01074.hp1 HG04204.hp1 |
intron_variant | MODIFIER | c.-80-10790G>A | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 1/7 | chr8 | 65659083 | ||||||
| chr8:65659426
|
G | GT | 7 | a0001c0001t0001g0093a0001c0001t0001g0172a0001c0001t0001g0182others(4): Show | 7 | HG01928.hp2 HG02622.hp1 NA18954.hp1 others(4): Show |
intron_variant | MODIFIER | c.-80-10430dupT | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr8 | 65659426 | |||||
| chr8:65659426
|
G | GTT | 41 | a0001c0001t0002g0001a0001c0001t0002g0039a0001c0001t0002g0042others(38): Show | 42 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(39): Show |
intron_variant | MODIFIER | c.-80-10431_-80-1043 others(6): Show |
MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr8 | 65659426 | |||||
| chr8:65659426
|
G | GTTT | 14 | a0001c0001t0003g0016a0001c0001t0003g0022a0001c0001t0003g0024others(11): Show | 14 | HG00140.hp1 HG00642.hp2 HG01168.hp2 others(11): Show |
intron_variant | MODIFIER | c.-80-10432_-80-1043 others(7): Show |
MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr8 | 65659426 | |||||
| chr8:65659426
|
G | GTTTT | 7 | a0001c0001t0003g0023a0001c0001t0003g0030a0001c0001t0003g0031others(4): Show | 7 | NA18939.hp1 NA18946.hp1 NA18951.hp1 others(4): Show |
intron_variant | MODIFIER | c.-80-10433_-80-1043 others(8): Show |
MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr8 | 65659426 | |||||
| chr8:65659426
|
GT | G | 69 | a0001c0001t0001g0074a0001c0001t0001g0075a0001c0001t0001g0079others(66): Show | 69 | HG00408.hp2 HG00438.hp1 HG00438.hp2 others(66): Show |
intron_variant | MODIFIER | c.-80-10430delT | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr8 | 65659426 | |||||
| chr8:65659438
|
T | C | 1 | a0001c0001t0001g0265 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.-80-10435T>C | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 1/7 | chr8 | 65659438 | ||||||
| chr8:65659456
|
C | T | 21 | a0001c0001t0003g0016a0001c0001t0003g0022a0001c0001t0003g0023others(18): Show | 21 | HG00140.hp1 HG00642.hp2 HG01168.hp2 others(18): Show |
intron_variant | MODIFIER | c.-80-10417C>T | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 1/7 | chr8 | 65659456 | ||||||
| chr8:65659498
|
G | A | 65 | a0001c0001t0002g0001a0001c0001t0002g0039a0001c0001t0002g0042others(62): Show | 66 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(63): Show |
intron_variant | MODIFIER | c.-80-10375G>A | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 1/7 | chr8 | 65659498 | ||||||
| chr8:65659599
|
C | CG | 4 | a0001c0001t0001g0146a0001c0001t0001g0175a0001c0001t0001g0274others(1): Show | 4 | HG00544.hp1 NA19067.hp1 NA19067.hp2 others(1): Show |
intron_variant | MODIFIER | c.-80-10270dupG | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr8 | 65659599 | |||||
| chr8:65659680
|
C | T | 77 | a0001c0001t0001g0071a0001c0001t0001g0072a0001c0001t0001g0073others(74): Show | 77 | HG00408.hp2 HG00438.hp1 HG00438.hp2 others(74): Show |
intron_variant | MODIFIER | c.-80-10193C>T | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 1/7 | chr8 | 65659680 | ||||||
| chr8:65659957
|
C | T | 11 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008others(8): Show | 11 | HG01255.hp2 HG01433.hp2 HG01891.hp1 others(8): Show |
intron_variant | MODIFIER | c.-80-9916C>T | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 1/7 | chr8 | 65659957 | ||||||
| chr8:65660215
|
T | C | 65 | a0001c0001t0002g0001a0001c0001t0002g0039a0001c0001t0002g0042others(62): Show | 66 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(63): Show |
intron_variant | MODIFIER | c.-80-9658T>C | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 1/7 | chr8 | 65660215 | ||||||
| chr8:65660291
|
C | CA | 30 | a0001c0001t0001g0002a0001c0001t0001g0085a0001c0001t0001g0086others(27): Show | 31 | HG00408.hp2 HG01168.hp2 HG02027.hp1 others(28): Show |
intron_variant | MODIFIER | c.-80-9564dupA | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr8 | 65660291 | |||||
| chr8:65660291
|
C | CAAA | 59 | a0001c0001t0002g0001a0001c0001t0002g0039a0001c0001t0002g0042others(56): Show | 60 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(57): Show |
intron_variant | MODIFIER | c.-80-9566_-80-9564d others(5): Show |
MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr8 | 65660291 | |||||
| chr8:65660291
|
CA | C | 14 | a0001c0001t0001g0136a0001c0001t0001g0219a0001c0001t0001g0279others(11): Show | 14 | HG01070.hp2 HG01071.hp1 HG01099.hp1 others(11): Show |
intron_variant | MODIFIER | c.-80-9564delA | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr8 | 65660291 | |||||
| chr8:65660310
|
G | A | 1 | a0001c0001t0003g0035 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.-80-9563G>A | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 1/7 | chr8 | 65660310 | ||||||
| chr8:65660312
|
C | CA | 16 | a0001c0001t0001g0192a0001c0001t0001g0238a0001c0001t0001g0247others(13): Show | 16 | HG01081.hp1 HG02148.hp1 HG02486.hp1 others(13): Show |
intron_variant | MODIFIER | c.-80-9551dupA | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr8 | 65660312 | |||||
| chr8:65660312
|
C | CAA | 31 | a0001c0001t0002g0001a0001c0001t0002g0039a0001c0001t0002g0042others(28): Show | 32 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(29): Show |
intron_variant | MODIFIER | c.-80-9552_-80-9551d others(4): Show |
MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr8 | 65660312 | |||||
| chr8:65660312
|
C | G | 1 | a0001c0001t0003g0035 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.-80-9561C>G | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 1/7 | chr8 | 65660312 | ||||||
| chr8:65660338
|
T | G | 1 | a0001c0001t0001g0242 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.-80-9535T>G | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 1/7 | chr8 | 65660338 | ||||||
| chr8:65660375
|
T | C | 65 | a0001c0001t0002g0001a0001c0001t0002g0039a0001c0001t0002g0042others(62): Show | 66 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(63): Show |
intron_variant | MODIFIER | c.-80-9498T>C | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 1/7 | chr8 | 65660375 | ||||||
| chr8:65660690
|
A | G | 2 | a0001c0001t0008g0011a0001c0001t0008g0012 | 2 | HG03130.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.-80-9183A>G | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 1/7 | chr8 | 65660690 | ||||||
| chr8:65660705
|
G | A | 21 | a0001c0001t0003g0016a0001c0001t0003g0022a0001c0001t0003g0023others(18): Show | 21 | HG00140.hp1 HG00642.hp2 HG01168.hp2 others(18): Show |
intron_variant | MODIFIER | c.-80-9168G>A | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 1/7 | chr8 | 65660705 | ||||||
| chr8:65661050
|
T | A | 65 | a0001c0001t0002g0001a0001c0001t0002g0039a0001c0001t0002g0042others(62): Show | 66 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(63): Show |
intron_variant | MODIFIER | c.-80-8823T>A | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 1/7 | chr8 | 65661050 | ||||||
| chr8:65661103
|
A | G | 65 | a0001c0001t0002g0001a0001c0001t0002g0039a0001c0001t0002g0042others(62): Show | 66 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(63): Show |
intron_variant | MODIFIER | c.-80-8770A>G | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 1/7 | chr8 | 65661103 | ||||||
| chr8:65661212
|
G | A | 3 | a0001c0001t0001g0223a0001c0001t0001g0261a0001c0001t0001g0316 | 3 | HG01168.hp1 HG01169.hp2 HG01433.hp1 |
intron_variant | MODIFIER | c.-80-8661G>A | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 1/7 | chr8 | 65661212 | ||||||
| chr8:65661326
|
C | T | 1 | a0001c0001t0005g0014 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.-80-8547C>T | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 1/7 | chr8 | 65661326 | ||||||
| chr8:65661349
|
C | T | 65 | a0001c0001t0002g0001a0001c0001t0002g0039a0001c0001t0002g0042others(62): Show | 66 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(63): Show |
intron_variant | MODIFIER | c.-80-8524C>T | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 1/7 | chr8 | 65661349 | ||||||
| chr8:65661378
|
C | T | 65 | a0001c0001t0002g0001a0001c0001t0002g0039a0001c0001t0002g0042others(62): Show | 66 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(63): Show |
intron_variant | MODIFIER | c.-80-8495C>T | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 1/7 | chr8 | 65661378 | ||||||
| chr8:65661380
|
G | A | 2 | a0001c0001t0001g0200a0001c0001t0001g0285 | 2 | HG03491.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.-80-8493G>A | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 1/7 | chr8 | 65661380 | ||||||
| chr8:65661512
|
C | T | 21 | a0001c0001t0003g0016a0001c0001t0003g0022a0001c0001t0003g0023others(18): Show | 21 | HG00140.hp1 HG00642.hp2 HG01168.hp2 others(18): Show |
intron_variant | MODIFIER | c.-80-8361C>T | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 1/7 | chr8 | 65661512 | ||||||
| chr8:65661546
|
G | A | 1 | a0001c0001t0008g0013 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.-80-8327G>A | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 1/7 | chr8 | 65661546 | ||||||
| chr8:65661600
|
G | A | 1 | a0001c0001t0001g0151 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.-80-8273G>A | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 1/7 | chr8 | 65661600 | ||||||
| chr8:65661807
|
T | C | 10 | a0001c0001t0001g0293a0001c0001t0001g0294a0001c0001t0001g0295others(7): Show | 10 | HG01070.hp2 HG01071.hp1 HG02258.hp1 others(7): Show |
intron_variant | MODIFIER | c.-80-8066T>C | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 1/7 | chr8 | 65661807 | ||||||
| chr8:65661964
|
AAAAC | A | 5 | a0001c0001t0001g0089a0001c0001t0001g0152a0001c0001t0001g0269others(2): Show | 5 | HG02258.hp1 HG02451.hp1 HG02965.hp2 others(2): Show |
intron_variant | MODIFIER | c.-80-7893_-80-7890d others(6): Show |
MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr8 | 65661964 | |||||
| chr8:65661980
|
C | A | 65 | a0001c0001t0002g0001a0001c0001t0002g0039a0001c0001t0002g0042others(62): Show | 66 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(63): Show |
intron_variant | MODIFIER | c.-80-7893C>A | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 1/7 | chr8 | 65661980 | ||||||
| chr8:65662002
|
C | CCTCTCCC others(5): Show |
1 | a0001c0001t0001g0145 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.-80-7843_-80-7832d others(14): Show |
MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr8 | 65662002 | |||||
| chr8:65662022
|
T | TCTCTCTC others(3): Show |
4 | a0001c0001t0001g0216a0001c0001t0001g0243a0001c0001t0001g0247others(1): Show | 4 | HG03704.hp1 NA18959.hp2 NA18989.hp1 others(1): Show |
intron_variant | MODIFIER | c.-80-7831_-80-7822d others(12): Show |
MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr8 | 65662022 | |||||
| chr8:65662022
|
TCTCTCTC others(3): Show |
T | 5 | a0001c0001t0001g0071a0001c0001t0001g0072a0001c0001t0001g0073others(2): Show | 5 | HG02559.hp2 HG02622.hp2 HG02970.hp1 others(2): Show |
intron_variant | MODIFIER | c.-80-7831_-80-7822d others(12): Show |
MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr8 | 65662022 | |||||
| chr8:65662026
|
TCTCTCCC others(77): Show |
T | 33 | a0001c0001t0003g0016a0001c0001t0003g0022a0001c0001t0003g0023others(30): Show | 33 | HG00140.hp1 HG00642.hp2 HG00733.hp1 others(30): Show |
intron_variant | MODIFIER | c.-80-7834_-80-7751d others(86): Show |
MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr8 | 65662026 | |||||
| chr8:65662032
|
C | CCT | 4 | a0001c0001t0001g0107a0001c0001t0001g0134a0001c0001t0001g0203others(1): Show | 4 | HG01106.hp2 HG02735.hp1 NA18947.hp2 others(1): Show |
intron_variant | MODIFIER | c.-80-7833_-80-7832d others(4): Show |
MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr8 | 65662032 | |||||
| chr8:65662032
|
C | CCTCTCTC others(7): Show |
52 | a0001c0001t0001g0079a0001c0001t0001g0080a0001c0001t0001g0083others(49): Show | 52 | HG00408.hp2 HG00438.hp1 HG00438.hp2 others(49): Show |
intron_variant | MODIFIER | c.-80-7832_-80-7831i others(16): Show |
MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr8 | 65662032 | |||||
| chr8:65662032
|
C | CCTCTCTC others(19): Show |
16 | a0001c0001t0001g0074a0001c0001t0001g0075a0001c0001t0001g0109others(13): Show | 16 | HG00642.hp1 HG01952.hp1 HG02300.hp2 others(13): Show |
intron_variant | MODIFIER | c.-80-7832_-80-7831i others(28): Show |
MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr8 | 65662032 | |||||
| chr8:65662032
|
C | CCTCTCTC others(31): Show |
1 | a0001c0001t0001g0280 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.-80-7832_-80-7831i others(40): Show |
MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr8 | 65662032 | |||||
| chr8:65662032
|
CCTCTCTC others(5): Show |
C | 7 | a0001c0001t0001g0242a0001c0001t0001g0313a0001c0001t0001g0314others(4): Show | 7 | HG01099.hp1 HG01261.hp2 HG01516.hp1 others(4): Show |
intron_variant | MODIFIER | c.-80-7812_-80-7801d others(14): Show |
MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr8 | 65662032 | |||||
| chr8:65662038
|
TCTCCCTC others(65): Show |
T | 32 | a0001c0001t0002g0001a0001c0001t0002g0039a0001c0001t0002g0042others(29): Show | 33 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(30): Show |
intron_variant | MODIFIER | c.-80-7831_-80-7760d others(74): Show |
MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr8 | 65662038 | |||||
| chr8:65662042
|
C | T | 3 | a0001c0001t0001g0085a0001c0001t0001g0086a0001c0001t0001g0087 | 3 | HG02257.hp2 HG03098.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.-80-7831C>T | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 1/7 | chr8 | 65662042 | ||||||
| chr8:65662044
|
T | C | 3 | a0001c0001t0001g0085a0001c0001t0001g0086a0001c0001t0001g0087 | 3 | HG02257.hp2 HG03098.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.-80-7829T>C | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 1/7 | chr8 | 65662044 | ||||||
| chr8:65662050
|
TCTCCCTC others(28): Show |
T | 3 | a0001c0001t0001g0085a0001c0001t0001g0086a0001c0001t0001g0087 | 3 | HG02257.hp2 HG03098.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.-80-7819_-80-7785d others(37): Show |
MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr8 | 65662050 | |||||
| chr8:65662060
|
TCTCTCCC others(18): Show |
T | 1 | a0001c0001t0001g0248 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.-80-7769_-80-7745d others(27): Show |
MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr8 | 65662060 | |||||
| chr8:65662072
|
TTTCCACA others(6): Show |
T | 1 | a0001c0001t0001g0107 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.-80-7800_-80-7788d others(15): Show |
MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 1/7 | chr8 | 65662072 | ||||||
| chr8:65662150
|
G | C | 23 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008others(20): Show | 23 | HG01109.hp1 HG01255.hp2 HG01433.hp2 others(20): Show |
intron_variant | MODIFIER | c.-80-7723G>C | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 1/7 | chr8 | 65662150 | ||||||
| chr8:65662249
|
C | T | 1 | a0001c0001t0001g0229 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.-80-7624C>T | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 1/7 | chr8 | 65662249 | ||||||
| chr8:65662346
|
A | G | 1 | a0001c0001t0001g0075 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.-80-7527A>G | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 1/7 | chr8 | 65662346 | ||||||
| chr8:65662360
|
G | C | 1 | a0001c0001t0001g0287 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.-80-7513G>C | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 1/7 | chr8 | 65662360 | ||||||
| chr8:65662400
|
C | T | 1 | a0001c0001t0001g0214 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.-80-7473C>T | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 1/7 | chr8 | 65662400 | ||||||
| chr8:65662431
|
G | C | 32 | a0001c0001t0002g0001a0001c0001t0002g0039a0001c0001t0002g0042others(29): Show | 33 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(30): Show |
intron_variant | MODIFIER | c.-80-7442G>C | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 1/7 | chr8 | 65662431 | ||||||
| chr8:65662438
|
G | C | 65 | a0001c0001t0002g0001a0001c0001t0002g0039a0001c0001t0002g0042others(62): Show | 66 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(63): Show |
intron_variant | MODIFIER | c.-80-7435G>C | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 1/7 | chr8 | 65662438 | ||||||
| chr8:65662491
|
G | C | 65 | a0001c0001t0002g0001a0001c0001t0002g0039a0001c0001t0002g0042others(62): Show | 66 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(63): Show |
intron_variant | MODIFIER | c.-80-7382G>C | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 1/7 | chr8 | 65662491 | ||||||
| chr8:65662518
|
A | AC | 38 | a0001c0001t0001g0007a0001c0001t0001g0093a0001c0001t0001g0105others(35): Show | 38 | HG00741.hp2 HG01071.hp2 HG01106.hp2 others(35): Show |
intron_variant | MODIFIER | c.-80-7351dupC | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr8 | 65662518 | |||||
| chr8:65662534
|
G | T | 65 | a0001c0001t0002g0001a0001c0001t0002g0039a0001c0001t0002g0042others(62): Show | 66 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(63): Show |
intron_variant | MODIFIER | c.-80-7339G>T | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 1/7 | chr8 | 65662534 | ||||||
| chr8:65662555
|
G | A | 3 | a0001c0001t0006g0340a0001c0001t0006g0341a0001c0001t0006g0342 | 3 | HG00733.hp1 HG01074.hp1 HG04204.hp1 |
intron_variant | MODIFIER | c.-80-7318G>A | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 1/7 | chr8 | 65662555 | ||||||
| chr8:65662581
|
T | C | 3 | a0001c0001t0005g0018a0001c0001t0005g0019a0001c0001t0005g0020 | 3 | HG03540.hp1 NA18906.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.-80-7292T>C | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 1/7 | chr8 | 65662581 | ||||||
| chr8:65662605
|
G | A | 65 | a0001c0001t0002g0001a0001c0001t0002g0039a0001c0001t0002g0042others(62): Show | 66 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(63): Show |
intron_variant | MODIFIER | c.-80-7268G>A | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 1/7 | chr8 | 65662605 | ||||||
| chr8:65662607
|
T | A | 65 | a0001c0001t0002g0001a0001c0001t0002g0039a0001c0001t0002g0042others(62): Show | 66 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(63): Show |
intron_variant | MODIFIER | c.-80-7266T>A | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 1/7 | chr8 | 65662607 | ||||||
| chr8:65662632
|
C | CCAT | 65 | a0001c0001t0002g0001a0001c0001t0002g0039a0001c0001t0002g0042others(62): Show | 66 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(63): Show |
intron_variant | MODIFIER | c.-80-7240_-80-7239i others(5): Show |
MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr8 | 65662632 | |||||
| chr8:65662640
|
G | A | 65 | a0001c0001t0002g0001a0001c0001t0002g0039a0001c0001t0002g0042others(62): Show | 66 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(63): Show |
intron_variant | MODIFIER | c.-80-7233G>A | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 1/7 | chr8 | 65662640 | ||||||
| chr8:65662641
|
A | G | 65 | a0001c0001t0002g0001a0001c0001t0002g0039a0001c0001t0002g0042others(62): Show | 66 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(63): Show |
intron_variant | MODIFIER | c.-80-7232A>G | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 1/7 | chr8 | 65662641 | ||||||
| chr8:65662653
|
A | C | 65 | a0001c0001t0002g0001a0001c0001t0002g0039a0001c0001t0002g0042others(62): Show | 66 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(63): Show |
intron_variant | MODIFIER | c.-80-7220A>C | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 1/7 | chr8 | 65662653 | ||||||
| chr8:65662654
|
C | G | 65 | a0001c0001t0002g0001a0001c0001t0002g0039a0001c0001t0002g0042others(62): Show | 66 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(63): Show |
intron_variant | MODIFIER | c.-80-7219C>G | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 1/7 | chr8 | 65662654 | ||||||
| chr8:65662655
|
C | T | 65 | a0001c0001t0002g0001a0001c0001t0002g0039a0001c0001t0002g0042others(62): Show | 66 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(63): Show |
intron_variant | MODIFIER | c.-80-7218C>T | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 1/7 | chr8 | 65662655 | ||||||
| chr8:65662663
|
T | C | 65 | a0001c0001t0002g0001a0001c0001t0002g0039a0001c0001t0002g0042others(62): Show | 66 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(63): Show |
intron_variant | MODIFIER | c.-80-7210T>C | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 1/7 | chr8 | 65662663 | ||||||
| chr8:65662665
|
G | GCCGCCCA others(66): Show |
65 | a0001c0001t0002g0001a0001c0001t0002g0039a0001c0001t0002g0042others(62): Show | 66 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(63): Show |
intron_variant | MODIFIER | c.-80-7207_-80-7206i others(75): Show |
MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr8 | 65662665 | |||||
| chr8:65662667
|
A | G | 65 | a0001c0001t0002g0001a0001c0001t0002g0039a0001c0001t0002g0042others(62): Show | 66 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(63): Show |
intron_variant | MODIFIER | c.-80-7206A>G | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 1/7 | chr8 | 65662667 | ||||||
| chr8:65662668
|
A | G | 65 | a0001c0001t0002g0001a0001c0001t0002g0039a0001c0001t0002g0042others(62): Show | 66 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(63): Show |
intron_variant | MODIFIER | c.-80-7205A>G | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 1/7 | chr8 | 65662668 | ||||||
| chr8:65662682
|
G | T | 1 | a0001c0001t0001g0268 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.-80-7191G>T | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 1/7 | chr8 | 65662682 | ||||||
| chr8:65662693
|
C | A | 65 | a0001c0001t0002g0001a0001c0001t0002g0039a0001c0001t0002g0042others(62): Show | 66 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(63): Show |
intron_variant | MODIFIER | c.-80-7180C>A | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 1/7 | chr8 | 65662693 | ||||||
| chr8:65662699
|
C | T | 65 | a0001c0001t0002g0001a0001c0001t0002g0039a0001c0001t0002g0042others(62): Show | 66 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(63): Show |
intron_variant | MODIFIER | c.-80-7174C>T | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 1/7 | chr8 | 65662699 | ||||||
| chr8:65662703
|
C | T | 65 | a0001c0001t0002g0001a0001c0001t0002g0039a0001c0001t0002g0042others(62): Show | 66 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(63): Show |
intron_variant | MODIFIER | c.-80-7170C>T | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 1/7 | chr8 | 65662703 | ||||||
| chr8:65662708
|
G | A | 65 | a0001c0001t0002g0001a0001c0001t0002g0039a0001c0001t0002g0042others(62): Show | 66 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(63): Show |
intron_variant | MODIFIER | c.-80-7165G>A | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 1/7 | chr8 | 65662708 | ||||||
| chr8:65662711
|
A | G | 65 | a0001c0001t0002g0001a0001c0001t0002g0039a0001c0001t0002g0042others(62): Show | 66 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(63): Show |
intron_variant | MODIFIER | c.-80-7162A>G | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 1/7 | chr8 | 65662711 | ||||||
| chr8:65662713
|
A | C | 65 | a0001c0001t0002g0001a0001c0001t0002g0039a0001c0001t0002g0042others(62): Show | 66 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(63): Show |
intron_variant | MODIFIER | c.-80-7160A>C | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 1/7 | chr8 | 65662713 | ||||||
| chr8:65662716
|
G | C | 3 | a0001c0001t0001g0085a0001c0001t0001g0086a0001c0001t0001g0087 | 3 | HG02257.hp2 HG03098.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.-80-7157G>C | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 1/7 | chr8 | 65662716 | ||||||
| chr8:65662753
|
C | A | 65 | a0001c0001t0002g0001a0001c0001t0002g0039a0001c0001t0002g0042others(62): Show | 66 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(63): Show |
intron_variant | MODIFIER | c.-80-7120C>A | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 1/7 | chr8 | 65662753 | ||||||
| chr8:65662793
|
C | T | 1 | a0001c0001t0001g0141 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.-80-7080C>T | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 1/7 | chr8 | 65662793 | ||||||
| chr8:65662838
|
A | G | 65 | a0001c0001t0002g0001a0001c0001t0002g0039a0001c0001t0002g0042others(62): Show | 66 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(63): Show |
intron_variant | MODIFIER | c.-80-7035A>G | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 1/7 | chr8 | 65662838 | ||||||
| chr8:65662843
|
G | A | 65 | a0001c0001t0002g0001a0001c0001t0002g0039a0001c0001t0002g0042others(62): Show | 66 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(63): Show |
intron_variant | MODIFIER | c.-80-7030G>A | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 1/7 | chr8 | 65662843 | ||||||
| chr8:65662874
|
A | C | 65 | a0001c0001t0002g0001a0001c0001t0002g0039a0001c0001t0002g0042others(62): Show | 66 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(63): Show |
intron_variant | MODIFIER | c.-80-6999A>C | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 1/7 | chr8 | 65662874 | ||||||
| chr8:65662924
|
G | A | 62 | a0001c0001t0002g0001a0001c0001t0002g0039a0001c0001t0002g0042others(59): Show | 63 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(60): Show |
intron_variant | MODIFIER | c.-80-6949G>A | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 1/7 | chr8 | 65662924 | ||||||
| chr8:65662943
|
C | T | 1 | a0001c0001t0001g0108 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.-80-6930C>T | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 1/7 | chr8 | 65662943 | ||||||
| chr8:65662945
|
G | C | 6 | a0001c0001t0001g0179a0001c0001t0001g0180a0001c0001t0001g0181others(3): Show | 6 | HG02155.hp2 NA18954.hp1 NA18967.hp1 others(3): Show |
intron_variant | MODIFIER | c.-80-6928G>C | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 1/7 | chr8 | 65662945 | ||||||
| chr8:65662963
|
C | G | 67 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(64): Show | 68 | HG00099.hp2 HG00323.hp2 HG00639.hp1 others(65): Show |
intron_variant | MODIFIER | c.-80-6910C>G | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 1/7 | chr8 | 65662963 | ||||||
| chr8:65662988
|
G | T | 65 | a0001c0001t0002g0001a0001c0001t0002g0039a0001c0001t0002g0042others(62): Show | 66 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(63): Show |
intron_variant | MODIFIER | c.-80-6885G>T | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 1/7 | chr8 | 65662988 | ||||||
| chr8:65663051
|
C | T | 32 | a0001c0001t0002g0001a0001c0001t0002g0039a0001c0001t0002g0042others(29): Show | 33 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(30): Show |
intron_variant | MODIFIER | c.-80-6822C>T | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 1/7 | chr8 | 65663051 | ||||||
| chr8:65663063
|
A | G | 9 | a0001c0001t0005g0014a0001c0001t0005g0015a0001c0001t0005g0018others(6): Show | 9 | HG02486.hp1 HG02647.hp2 HG02965.hp1 others(6): Show |
intron_variant | MODIFIER | c.-80-6810A>G | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 1/7 | chr8 | 65663063 | ||||||
| chr8:65663180
|
A | G | 1 | a0001c0001t0001g0203 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.-80-6693A>G | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 1/7 | chr8 | 65663180 | ||||||
| chr8:65663242
|
T | C | 8 | a0001c0001t0001g0189a0001c0001t0001g0234a0001c0001t0001g0235others(5): Show | 8 | HG01243.hp1 HG01884.hp1 HG02559.hp1 others(5): Show |
intron_variant | MODIFIER | c.-80-6631T>C | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 1/7 | chr8 | 65663242 | ||||||
| chr8:65663246
|
C | T | 65 | a0001c0001t0002g0001a0001c0001t0002g0039a0001c0001t0002g0042others(62): Show | 66 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(63): Show |
intron_variant | MODIFIER | c.-80-6627C>T | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 1/7 | chr8 | 65663246 | ||||||
| chr8:65663258
|
T | C | 21 | a0001c0001t0003g0016a0001c0001t0003g0022a0001c0001t0003g0023others(18): Show | 21 | HG00140.hp1 HG00642.hp2 HG01168.hp2 others(18): Show |
intron_variant | MODIFIER | c.-80-6615T>C | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 1/7 | chr8 | 65663258 | ||||||
| chr8:65663356
|
A | G | 3 | a0001c0001t0003g0016a0001c0001t0003g0022a0001c0001t0003g0029 | 3 | HG00140.hp1 HG00642.hp2 HG01496.hp2 |
intron_variant | MODIFIER | c.-80-6517A>G | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 1/7 | chr8 | 65663356 | ||||||
| chr8:65663393
|
T | C | 65 | a0001c0001t0002g0001a0001c0001t0002g0039a0001c0001t0002g0042others(62): Show | 66 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(63): Show |
intron_variant | MODIFIER | c.-80-6480T>C | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 1/7 | chr8 | 65663393 | ||||||
| chr8:65663394
|
G | C | 21 | a0001c0001t0003g0016a0001c0001t0003g0022a0001c0001t0003g0023others(18): Show | 21 | HG00140.hp1 HG00642.hp2 HG01168.hp2 others(18): Show |
intron_variant | MODIFIER | c.-80-6479G>C | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 1/7 | chr8 | 65663394 | ||||||
| chr8:65663516
|
A | G | 5 | a0001c0001t0001g0079a0001c0001t0001g0107a0001c0001t0001g0197others(2): Show | 5 | HG01106.hp2 HG02257.hp1 HG02698.hp1 others(2): Show |
intron_variant | MODIFIER | c.-80-6357A>G | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 1/7 | chr8 | 65663516 | ||||||
| chr8:65663529
|
T | TA | 88 | a0001c0001t0001g0002a0001c0001t0001g0071a0001c0001t0001g0072others(85): Show | 89 | HG00408.hp2 HG00438.hp1 HG00438.hp2 others(86): Show |
intron_variant | MODIFIER | c.-80-6326dupA | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr8 | 65663529 | |||||
| chr8:65663529
|
TA | T | 69 | a0001c0001t0001g0101a0001c0001t0001g0229a0001c0001t0001g0253others(66): Show | 70 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(67): Show |
intron_variant | MODIFIER | c.-80-6326delA | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr8 | 65663529 | |||||
| chr8:65663529
|
TAA | T | 6 | a0001c0001t0002g0042a0001c0001t0002g0068a0001c0001t0002g0069others(3): Show | 6 | HG02109.hp2 HG03195.hp1 HG03471.hp2 others(3): Show |
intron_variant | MODIFIER | c.-80-6327_-80-6326d others(4): Show |
MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr8 | 65663529 | |||||
| chr8:65663631
|
A | AT | 65 | a0001c0001t0002g0001a0001c0001t0002g0039a0001c0001t0002g0042others(62): Show | 66 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(63): Show |
intron_variant | MODIFIER | c.-80-6241dupT | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr8 | 65663631 | |||||
| chr8:65663822
|
C | CT | 19 | a0001c0001t0001g0085a0001c0001t0001g0086a0001c0001t0001g0087others(16): Show | 19 | HG02027.hp2 HG02148.hp1 HG02257.hp2 others(16): Show |
intron_variant | MODIFIER | c.-80-6031dupT | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr8 | 65663822 | |||||
| chr8:65663822
|
CT | C | 30 | a0001c0001t0001g0097a0001c0001t0001g0136a0001c0001t0001g0176others(27): Show | 30 | HG00642.hp2 HG01069.hp1 HG01168.hp2 others(27): Show |
intron_variant | MODIFIER | c.-80-6031delT | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr8 | 65663822 | |||||
| chr8:65663913
|
C | T | 2 | a0001c0001t0001g0321a0001c0001t0001g0334 | 2 | HG01081.hp1 HG01106.hp1 |
intron_variant | MODIFIER | c.-80-5960C>T | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 1/7 | chr8 | 65663913 | ||||||
| chr8:65663988
|
G | C | 1 | a0001c0001t0001g0196 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.-80-5885G>C | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 1/7 | chr8 | 65663988 | ||||||
| chr8:65664005
|
G | A | 3 | a0001c0001t0001g0085a0001c0001t0001g0086a0001c0001t0001g0087 | 3 | HG02257.hp2 HG03098.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.-80-5868G>A | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 1/7 | chr8 | 65664005 | ||||||
| chr8:65664084
|
A | G | 14 | a0001c0001t0004g0076a0001c0001t0004g0077a0001c0001t0004g0078others(11): Show | 14 | HG00438.hp2 HG01099.hp2 HG01934.hp1 others(11): Show |
intron_variant | MODIFIER | c.-80-5789A>G | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 1/7 | chr8 | 65664084 | ||||||
| chr8:65664117
|
T | C | 1 | a0001c0001t0001g0339 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.-80-5756T>C | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 1/7 | chr8 | 65664117 | ||||||
| chr8:65664185
|
C | T | 1 | a0001c0001t0004g0140 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.-80-5688C>T | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 1/7 | chr8 | 65664185 | ||||||
| chr8:65664579
|
C | T | 21 | a0001c0001t0003g0016a0001c0001t0003g0022a0001c0001t0003g0023others(18): Show | 21 | HG00140.hp1 HG00642.hp2 HG01168.hp2 others(18): Show |
intron_variant | MODIFIER | c.-80-5294C>T | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 1/7 | chr8 | 65664579 | ||||||
| chr8:65664610
|
G | GT | 11 | a0001c0001t0001g0080a0001c0001t0001g0141a0001c0001t0001g0171others(8): Show | 11 | HG02074.hp1 HG02135.hp2 HG02293.hp2 others(8): Show |
intron_variant | MODIFIER | c.-80-5245dupT | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr8 | 65664610 | |||||
| chr8:65664610
|
G | T | 1 | a0001c0001t0002g0062 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.-80-5263G>T | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 1/7 | chr8 | 65664610 | ||||||
| chr8:65664610
|
GT | G | 15 | a0001c0001t0001g0183a0001c0001t0001g0224a0001c0001t0001g0225others(12): Show | 15 | HG01069.hp1 HG01109.hp1 HG01243.hp2 others(12): Show |
intron_variant | MODIFIER | c.-80-5245delT | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr8 | 65664610 | |||||
| chr8:65664615
|
T | G | 3 | a0001c0001t0006g0340a0001c0001t0006g0341a0001c0001t0006g0342 | 3 | HG00733.hp1 HG01074.hp1 HG04204.hp1 |
intron_variant | MODIFIER | c.-80-5258T>G | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 1/7 | chr8 | 65664615 | ||||||
| chr8:65664616
|
T | G | 9 | a0001c0001t0001g0002a0001c0001t0001g0094a0001c0001t0001g0096others(6): Show | 10 | HG02895.hp2 HG02897.hp2 NA18957.hp2 others(7): Show |
intron_variant | MODIFIER | c.-80-5257T>G | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 1/7 | chr8 | 65664616 | ||||||
| chr8:65664633
|
A | G | 65 | a0001c0001t0002g0001a0001c0001t0002g0039a0001c0001t0002g0042others(62): Show | 66 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(63): Show |
intron_variant | MODIFIER | c.-80-5240A>G | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 1/7 | chr8 | 65664633 | ||||||
| chr8:65664688
|
C | G | 1 | a0001c0001t0008g0013 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.-80-5185C>G | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 1/7 | chr8 | 65664688 | ||||||
| chr8:65664772
|
G | T | 3 | a0001c0001t0006g0340a0001c0001t0006g0341a0001c0001t0006g0342 | 3 | HG00733.hp1 HG01074.hp1 HG04204.hp1 |
intron_variant | MODIFIER | c.-80-5101G>T | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 1/7 | chr8 | 65664772 | ||||||
| chr8:65664839
|
T | C | 65 | a0001c0001t0002g0001a0001c0001t0002g0039a0001c0001t0002g0042others(62): Show | 66 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(63): Show |
intron_variant | MODIFIER | c.-80-5034T>C | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 1/7 | chr8 | 65664839 | ||||||
| chr8:65664845
|
C | T | 1 | a0001c0001t0001g0170 | 1 | HG01517.hp2 | intron_variant | MODIFIER | c.-80-5028C>T | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 1/7 | chr8 | 65664845 | ||||||
| chr8:65664878
|
G | A | 2 | a0001c0001t0001g0229a0001c0001t0001g0307 | 2 | HG01167.hp1 HG01891.hp1 |
intron_variant | MODIFIER | c.-80-4995G>A | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 1/7 | chr8 | 65664878 | ||||||
| chr8:65664911
|
T | G | 43 | a0001c0001t0001g0005a0001c0001t0001g0189a0001c0001t0001g0223others(40): Show | 44 | HG00099.hp2 HG00323.hp2 HG00639.hp1 others(41): Show |
intron_variant | MODIFIER | c.-80-4962T>G | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 1/7 | chr8 | 65664911 | ||||||
| chr8:65664933
|
A | AT | 84 | a0001c0001t0001g0071a0001c0001t0001g0072a0001c0001t0001g0073others(81): Show | 84 | HG00408.hp2 HG00438.hp1 HG00438.hp2 others(81): Show |
intron_variant | MODIFIER | c.-80-4919dupT | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr8 | 65664933 | |||||
| chr8:65664933
|
A | ATT | 9 | a0001c0001t0001g0087a0001c0001t0001g0120a0001c0001t0001g0123others(6): Show | 9 | HG02074.hp1 HG02135.hp2 HG02257.hp1 others(6): Show |
intron_variant | MODIFIER | c.-80-4920_-80-4919d others(4): Show |
MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr8 | 65664933 | |||||
| chr8:65664933
|
A | T | 14 | a0001c0001t0001g0002a0001c0001t0001g0094a0001c0001t0001g0095others(11): Show | 15 | HG02027.hp1 HG02055.hp2 HG02486.hp2 others(12): Show |
intron_variant | MODIFIER | c.-80-4940A>T | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 1/7 | chr8 | 65664933 | ||||||
| chr8:65664933
|
AT | A | 63 | a0001c0001t0001g0148a0001c0001t0001g0176a0001c0001t0001g0206others(60): Show | 64 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(61): Show |
intron_variant | MODIFIER | c.-80-4919delT | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr8 | 65664933 | |||||
| chr8:65664936
|
T | A | 3 | a0001c0001t0006g0340a0001c0001t0006g0341a0001c0001t0006g0342 | 3 | HG00733.hp1 HG01074.hp1 HG04204.hp1 |
intron_variant | MODIFIER | c.-80-4937T>A | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 1/7 | chr8 | 65664936 | ||||||
| chr8:65665010
|
C | T | 1 | a0001c0001t0001g0101 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.-80-4863C>T | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 1/7 | chr8 | 65665010 | ||||||
| chr8:65665082
|
G | A | 32 | a0001c0001t0002g0001a0001c0001t0002g0039a0001c0001t0002g0042others(29): Show | 33 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(30): Show |
intron_variant | MODIFIER | c.-80-4791G>A | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 1/7 | chr8 | 65665082 | ||||||
| chr8:65665601
|
A | C | 23 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008others(20): Show | 23 | HG01109.hp1 HG01255.hp2 HG01433.hp2 others(20): Show |
intron_variant | MODIFIER | c.-80-4272A>C | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 1/7 | chr8 | 65665601 | ||||||
| chr8:65665639
|
G | A | 2 | a0001c0001t0001g0168a0001c0001t0012g0144 | 2 | HG01123.hp2 HG04184.hp1 |
intron_variant | MODIFIER | c.-80-4234G>A | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 1/7 | chr8 | 65665639 | ||||||
| chr8:65665914
|
TA | T | 65 | a0001c0001t0002g0001a0001c0001t0002g0039a0001c0001t0002g0042others(62): Show | 66 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(63): Show |
intron_variant | MODIFIER | c.-80-3957delA | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr8 | 65665914 | |||||
| chr8:65665930
|
T | C | 65 | a0001c0001t0002g0001a0001c0001t0002g0039a0001c0001t0002g0042others(62): Show | 66 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(63): Show |
intron_variant | MODIFIER | c.-80-3943T>C | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 1/7 | chr8 | 65665930 | ||||||
| chr8:65665989
|
T | C | 1 | a0001c0001t0001g0282 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.-80-3884T>C | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 1/7 | chr8 | 65665989 | ||||||
| chr8:65666105
|
T | A | 65 | a0001c0001t0002g0001a0001c0001t0002g0039a0001c0001t0002g0042others(62): Show | 66 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(63): Show |
intron_variant | MODIFIER | c.-80-3768T>A | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 1/7 | chr8 | 65666105 | ||||||
| chr8:65666111
|
A | G | 9 | a0001c0001t0005g0014a0001c0001t0005g0015a0001c0001t0005g0018others(6): Show | 9 | HG02486.hp1 HG02647.hp2 HG02965.hp1 others(6): Show |
intron_variant | MODIFIER | c.-80-3762A>G | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 1/7 | chr8 | 65666111 | ||||||
| chr8:65666170
|
G | C | 1 | a0001c0001t0001g0249 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.-80-3703G>C | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 1/7 | chr8 | 65666170 | ||||||
| chr8:65666295
|
T | TA | 65 | a0001c0001t0002g0001a0001c0001t0002g0039a0001c0001t0002g0042others(62): Show | 66 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(63): Show |
intron_variant | MODIFIER | c.-80-3578_-80-3577i others(3): Show |
MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 1/7 | chr8 | 65666295 | ||||||
| chr8:65666526
|
G | A | 3 | a0001c0001t0006g0340a0001c0001t0006g0341a0001c0001t0006g0342 | 3 | HG00733.hp1 HG01074.hp1 HG04204.hp1 |
intron_variant | MODIFIER | c.-80-3347G>A | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 1/7 | chr8 | 65666526 | ||||||
| chr8:65666879
|
C | T | 1 | a0001c0001t0008g0011 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.-80-2994C>T | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 1/7 | chr8 | 65666879 | ||||||
| chr8:65666924
|
T | C | 4 | a0001c0001t0002g0047a0001c0001t0002g0048a0001c0001t0002g0065others(1): Show | 4 | HG00741.hp1 HG01192.hp1 HG01928.hp1 others(1): Show |
intron_variant | MODIFIER | c.-80-2949T>C | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 1/7 | chr8 | 65666924 | ||||||
| chr8:65666997
|
A | G | 256 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0006others(253): Show | 259 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(256): Show |
intron_variant | MODIFIER | c.-80-2876A>G | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 1/7 | chr8 | 65666997 | ||||||
| chr8:65667010
|
C | A | 65 | a0001c0001t0002g0001a0001c0001t0002g0039a0001c0001t0002g0042others(62): Show | 66 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(63): Show |
intron_variant | MODIFIER | c.-80-2863C>A | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 1/7 | chr8 | 65667010 | ||||||
| chr8:65667023
|
C | T | 65 | a0001c0001t0002g0001a0001c0001t0002g0039a0001c0001t0002g0042others(62): Show | 66 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(63): Show |
intron_variant | MODIFIER | c.-80-2850C>T | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 1/7 | chr8 | 65667023 | ||||||
| chr8:65667090
|
C | T | 1 | a0001c0001t0001g0246 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.-80-2783C>T | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 1/7 | chr8 | 65667090 | ||||||
| chr8:65667107
|
G | T | 3 | a0001c0001t0006g0340a0001c0001t0006g0341a0001c0001t0006g0342 | 3 | HG00733.hp1 HG01074.hp1 HG04204.hp1 |
intron_variant | MODIFIER | c.-80-2766G>T | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 1/7 | chr8 | 65667107 | ||||||
| chr8:65667201
|
G | A | 1 | a0001c0001t0001g0244 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.-80-2672G>A | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 1/7 | chr8 | 65667201 | ||||||
| chr8:65667208
|
A | G | 65 | a0001c0001t0002g0001a0001c0001t0002g0039a0001c0001t0002g0042others(62): Show | 66 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(63): Show |
intron_variant | MODIFIER | c.-80-2665A>G | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 1/7 | chr8 | 65667208 | ||||||
| chr8:65667215
|
G | A | 1 | a0001c0001t0001g0260 | 1 | HG01258.hp1 | intron_variant | MODIFIER | c.-80-2658G>A | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 1/7 | chr8 | 65667215 | ||||||
| chr8:65667276
|
CA | C | 64 | a0001c0001t0002g0001a0001c0001t0002g0039a0001c0001t0002g0042others(61): Show | 65 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(62): Show |
intron_variant | MODIFIER | c.-80-2585delA | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr8 | 65667276 | |||||
| chr8:65667346
|
G | GT | 13 | a0001c0001t0001g0010a0001c0001t0001g0146a0001c0001t0001g0224others(10): Show | 13 | HG02135.hp2 HG02486.hp1 HG02559.hp1 others(10): Show |
intron_variant | MODIFIER | c.-80-2516dupT | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr8 | 65667346 | |||||
| chr8:65667346
|
G | GTT | 58 | a0001c0001t0002g0001a0001c0001t0002g0039a0001c0001t0002g0042others(55): Show | 59 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(56): Show |
intron_variant | MODIFIER | c.-80-2517_-80-2516d others(4): Show |
MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr8 | 65667346 | |||||
| chr8:65667461
|
C | G | 32 | a0001c0001t0002g0001a0001c0001t0002g0039a0001c0001t0002g0042others(29): Show | 33 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(30): Show |
intron_variant | MODIFIER | c.-80-2412C>G | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 1/7 | chr8 | 65667461 | ||||||
| chr8:65667479
|
G | A | 2 | a0001c0001t0001g0266a0001c0001t0001g0306 | 2 | HG01255.hp2 HG01433.hp2 |
intron_variant | MODIFIER | c.-80-2394G>A | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 1/7 | chr8 | 65667479 | ||||||
| chr8:65667521
|
G | A | 41 | a0001c0001t0002g0001a0001c0001t0002g0039a0001c0001t0002g0042others(38): Show | 42 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(39): Show |
intron_variant | MODIFIER | c.-80-2352G>A | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 1/7 | chr8 | 65667521 | ||||||
| chr8:65667638
|
G | A | 65 | a0001c0001t0002g0001a0001c0001t0002g0039a0001c0001t0002g0042others(62): Show | 66 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(63): Show |
intron_variant | MODIFIER | c.-80-2235G>A | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 1/7 | chr8 | 65667638 | ||||||
| chr8:65667722
|
T | C | 65 | a0001c0001t0002g0001a0001c0001t0002g0039a0001c0001t0002g0042others(62): Show | 66 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(63): Show |
intron_variant | MODIFIER | c.-80-2151T>C | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 1/7 | chr8 | 65667722 | ||||||
| chr8:65667726
|
C | G | 9 | a0001c0001t0005g0014a0001c0001t0005g0015a0001c0001t0005g0018others(6): Show | 9 | HG02486.hp1 HG02647.hp2 HG02965.hp1 others(6): Show |
intron_variant | MODIFIER | c.-80-2147C>G | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 1/7 | chr8 | 65667726 | ||||||
| chr8:65667838
|
T | C | 15 | a0001c0001t0001g0002a0001c0001t0001g0094a0001c0001t0001g0095others(12): Show | 16 | HG02027.hp1 HG02055.hp2 HG02486.hp2 others(13): Show |
intron_variant | MODIFIER | c.-80-2035T>C | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 1/7 | chr8 | 65667838 | ||||||
| chr8:65667978
|
C | G | 1 | a0001c0001t0006g0342 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.-80-1895C>G | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 1/7 | chr8 | 65667978 | ||||||
| chr8:65667982
|
A | G | 10 | a0001c0001t0001g0293a0001c0001t0001g0294a0001c0001t0001g0295others(7): Show | 10 | HG01070.hp2 HG01071.hp1 HG02258.hp1 others(7): Show |
intron_variant | MODIFIER | c.-80-1891A>G | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 1/7 | chr8 | 65667982 | ||||||
| chr8:65668028
|
T | G | 9 | a0001c0001t0005g0014a0001c0001t0005g0015a0001c0001t0005g0018others(6): Show | 9 | HG02486.hp1 HG02647.hp2 HG02965.hp1 others(6): Show |
intron_variant | MODIFIER | c.-80-1845T>G | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 1/7 | chr8 | 65668028 | ||||||
| chr8:65668049
|
C | T | 9 | a0001c0001t0005g0014a0001c0001t0005g0015a0001c0001t0005g0018others(6): Show | 9 | HG02486.hp1 HG02647.hp2 HG02965.hp1 others(6): Show |
intron_variant | MODIFIER | c.-80-1824C>T | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 1/7 | chr8 | 65668049 | ||||||
| chr8:65668183
|
T | C | 2 | a0001c0001t0001g0275a0001c0001t0007g0193 | 2 | NA18957.hp1 NA18993.hp1 |
intron_variant | MODIFIER | c.-80-1690T>C | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 1/7 | chr8 | 65668183 | ||||||
| chr8:65668184
|
C | CT | 92 | a0001c0001t0001g0002a0001c0001t0001g0072a0001c0001t0001g0073others(89): Show | 93 | HG00408.hp2 HG00438.hp1 HG00438.hp2 others(90): Show |
intron_variant | MODIFIER | c.-80-1678dupT | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr8 | 65668184 | |||||
| chr8:65668184
|
C | T | 4 | a0001c0001t0001g0275a0001c0001t0001g0283a0001c0001t0002g0053others(1): Show | 4 | HG02074.hp1 NA18957.hp1 NA18989.hp2 others(1): Show |
intron_variant | MODIFIER | c.-80-1689C>T | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 1/7 | chr8 | 65668184 | ||||||
| chr8:65668184
|
CT | C | 14 | a0001c0001t0001g0222a0001c0001t0001g0243a0001c0001t0001g0249others(11): Show | 14 | HG01192.hp2 HG01884.hp2 HG01891.hp2 others(11): Show |
intron_variant | MODIFIER | c.-80-1678delT | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr8 | 65668184 | |||||
| chr8:65668323
|
G | A | 1 | a0001c0001t0001g0302 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.-80-1550G>A | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 1/7 | chr8 | 65668323 | ||||||
| chr8:65668344
|
AT | A | 195 | a0001c0001t0001g0071a0001c0001t0001g0072a0001c0001t0001g0073others(192): Show | 196 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(193): Show |
intron_variant | MODIFIER | c.-80-1514delT | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr8 | 65668344 | |||||
| chr8:65668400
|
T | C | 3 | a0001c0001t0006g0340a0001c0001t0006g0341a0001c0001t0006g0342 | 3 | HG00733.hp1 HG01074.hp1 HG04204.hp1 |
intron_variant | MODIFIER | c.-80-1473T>C | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 1/7 | chr8 | 65668400 | ||||||
| chr8:65668416
|
G | C | 4 | a0001c0001t0001g0121a0001c0001t0001g0124a0001c0001t0001g0196others(1): Show | 4 | HG00438.hp1 NA18944.hp1 NA18956.hp2 others(1): Show |
intron_variant | MODIFIER | c.-80-1457G>C | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 1/7 | chr8 | 65668416 | ||||||
| chr8:65668435
|
G | A | 2 | a0001c0001t0001g0122a0001c0001t0001g0125 | 2 | HG02155.hp1 NA18987.hp2 |
intron_variant | MODIFIER | c.-80-1438G>A | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 1/7 | chr8 | 65668435 | ||||||
| chr8:65668467
|
CATG | C | 10 | a0001c0001t0001g0293a0001c0001t0001g0294a0001c0001t0001g0295others(7): Show | 10 | HG01070.hp2 HG01071.hp1 HG02258.hp1 others(7): Show |
intron_variant | MODIFIER | c.-80-1404_-80-1402d others(5): Show |
MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr8 | 65668467 | |||||
| chr8:65668468
|
A | G | 1 | a0001c0001t0001g0339 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.-80-1405A>G | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 1/7 | chr8 | 65668468 | ||||||
| chr8:65668477
|
C | T | 21 | a0001c0001t0003g0016a0001c0001t0003g0022a0001c0001t0003g0023others(18): Show | 21 | HG00140.hp1 HG00642.hp2 HG01168.hp2 others(18): Show |
intron_variant | MODIFIER | c.-80-1396C>T | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 1/7 | chr8 | 65668477 | ||||||
| chr8:65668525
|
C | CT | 99 | a0001c0001t0001g0005a0001c0001t0001g0176a0001c0001t0001g0206others(96): Show | 101 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(98): Show |
intron_variant | MODIFIER | c.-80-1331dupT | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr8 | 65668525 | |||||
| chr8:65668525
|
CT | C | 7 | a0001c0001t0001g0136a0001c0001t0001g0189a0001c0001t0001g0229others(4): Show | 7 | HG01167.hp1 HG02698.hp1 HG02809.hp1 others(4): Show |
intron_variant | MODIFIER | c.-80-1331delT | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr8 | 65668525 | |||||
| chr8:65668534
|
T | C | 1 | a0001c0001t0001g0221 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.-80-1339T>C | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 1/7 | chr8 | 65668534 | ||||||
| chr8:65668584
|
G | T | 1 | a0001c0001t0001g0279 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.-80-1289G>T | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 1/7 | chr8 | 65668584 | ||||||
| chr8:65668587
|
A | C | 1 | a0001c0001t0001g0279 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.-80-1286A>C | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 1/7 | chr8 | 65668587 | ||||||
| chr8:65668608
|
G | A | 1 | a0001c0001t0001g0305 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.-80-1265G>A | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 1/7 | chr8 | 65668608 | ||||||
| chr8:65668682
|
T | C | 1 | a0001c0001t0001g0326 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.-80-1191T>C | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 1/7 | chr8 | 65668682 | ||||||
| chr8:65668810
|
G | A | 2 | a0001c0001t0001g0324a0001c0001t0001g0325 | 2 | HG01516.hp1 HG01517.hp1 |
intron_variant | MODIFIER | c.-80-1063G>A | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 1/7 | chr8 | 65668810 | ||||||
| chr8:65668823
|
T | A | 3 | a0001c0001t0006g0340a0001c0001t0006g0341a0001c0001t0006g0342 | 3 | HG00733.hp1 HG01074.hp1 HG04204.hp1 |
intron_variant | MODIFIER | c.-80-1050T>A | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 1/7 | chr8 | 65668823 | ||||||
| chr8:65669002
|
G | A | 1 | a0001c0001t0001g0300 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.-80-871G>A | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 1/7 | chr8 | 65669002 | ||||||
| chr8:65669064
|
C | A | 1 | a0001c0001t0001g0108 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.-80-809C>A | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 1/7 | chr8 | 65669064 | ||||||
| chr8:65669418
|
A | G | 3 | a0001c0001t0001g0085a0001c0001t0001g0086a0001c0001t0001g0087 | 3 | HG02257.hp2 HG03098.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.-80-455A>G | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 1/7 | chr8 | 65669418 | ||||||
| chr8:65669476
|
A | G | 1 | a0001c0001t0001g0218 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.-80-397A>G | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 1/7 | chr8 | 65669476 | ||||||
| chr8:65669556
|
G | GT | 8 | a0001c0001t0001g0116a0001c0001t0001g0119a0001c0001t0001g0131others(5): Show | 8 | HG00642.hp1 HG01952.hp1 HG02148.hp2 others(5): Show |
intron_variant | MODIFIER | c.-80-304dupT | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr8 | 65669556 | |||||
| chr8:65669628
|
C | T | 1 | a0001c0001t0001g0230 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.-80-245C>T | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 1/7 | chr8 | 65669628 | ||||||
| chr8:65670436
|
A | G | 1 | a0001c0001t0001g0278 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.66+418A>G | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 2/7 | chr8 | 65670436 | ||||||
| chr8:65670506
|
G | A | 1 | a0001c0001t0001g0178 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.66+488G>A | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 2/7 | chr8 | 65670506 | ||||||
| chr8:65670592
|
T | C | 81 | a0001c0001t0001g0071a0001c0001t0001g0072a0001c0001t0001g0073others(78): Show | 81 | HG00408.hp2 HG00438.hp1 HG00438.hp2 others(78): Show |
intron_variant | MODIFIER | c.66+574T>C | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 2/7 | chr8 | 65670592 | ||||||
| chr8:65670631
|
T | G | 1 | a0001c0001t0001g0337 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.66+613T>G | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 2/7 | chr8 | 65670631 | ||||||
| chr8:65670707
|
C | CT | 61 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(58): Show | 63 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(60): Show |
intron_variant | MODIFIER | c.66+703dupT | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr8 | 65670707 | |||||
| chr8:65670765
|
A | C | 15 | a0001c0001t0001g0002a0001c0001t0001g0094a0001c0001t0001g0095others(12): Show | 16 | HG02027.hp1 HG02055.hp2 HG02486.hp2 others(13): Show |
intron_variant | MODIFIER | c.66+747A>C | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 2/7 | chr8 | 65670765 | ||||||
| chr8:65670799
|
G | A | 15 | a0001c0001t0001g0002a0001c0001t0001g0094a0001c0001t0001g0095others(12): Show | 16 | HG02027.hp1 HG02055.hp2 HG02486.hp2 others(13): Show |
intron_variant | MODIFIER | c.66+781G>A | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 2/7 | chr8 | 65670799 | ||||||
| chr8:65671023
|
T | C | 1 | a0001c0001t0001g0287 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.66+1005T>C | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 2/7 | chr8 | 65671023 | ||||||
| chr8:65671090
|
G | A | 3 | a0001c0001t0001g0085a0001c0001t0001g0086a0001c0001t0001g0087 | 3 | HG02257.hp2 HG03098.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.66+1072G>A | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 2/7 | chr8 | 65671090 | ||||||
| chr8:65671102
|
G | T | 5 | a0001c0001t0001g0071a0001c0001t0001g0072a0001c0001t0001g0073others(2): Show | 5 | HG02559.hp2 HG02622.hp2 HG02970.hp1 others(2): Show |
intron_variant | MODIFIER | c.66+1084G>T | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 2/7 | chr8 | 65671102 | ||||||
| chr8:65671540
|
T | TA | 69 | a0001c0001t0001g0074a0001c0001t0001g0075a0001c0001t0001g0079others(66): Show | 69 | HG00408.hp2 HG00438.hp1 HG00438.hp2 others(66): Show |
intron_variant | MODIFIER | c.66+1542dupA | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr8 | 65671540 | |||||
| chr8:65671540
|
TA | T | 9 | a0001c0001t0001g0150a0001c0001t0001g0167a0001c0001t0001g0276others(6): Show | 9 | HG00323.hp2 HG01069.hp1 HG01081.hp1 others(6): Show |
intron_variant | MODIFIER | c.66+1542delA | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr8 | 65671540 | |||||
| chr8:65671561
|
G | A | 3 | a0001c0001t0006g0340a0001c0001t0006g0341a0001c0001t0006g0342 | 3 | HG00733.hp1 HG01074.hp1 HG04204.hp1 |
intron_variant | MODIFIER | c.66+1543G>A | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 2/7 | chr8 | 65671561 | ||||||
| chr8:65671693
|
A | G | 1 | a0001c0001t0001g0314 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.66+1675A>G | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 2/7 | chr8 | 65671693 | ||||||
| chr8:65671783
|
T | A | 51 | a0001c0001t0001g0074a0001c0001t0001g0080a0001c0001t0001g0083others(48): Show | 51 | HG00408.hp2 HG00438.hp1 HG00438.hp2 others(48): Show |
intron_variant | MODIFIER | c.66+1765T>A | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 2/7 | chr8 | 65671783 | ||||||
| chr8:65671784
|
G | T | 51 | a0001c0001t0001g0074a0001c0001t0001g0080a0001c0001t0001g0083others(48): Show | 51 | HG00408.hp2 HG00438.hp1 HG00438.hp2 others(48): Show |
intron_variant | MODIFIER | c.66+1766G>T | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 2/7 | chr8 | 65671784 | ||||||
| chr8:65671869
|
A | C | 1 | a0001c0001t0001g0141 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.66+1851A>C | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 2/7 | chr8 | 65671869 | ||||||
| chr8:65672033
|
G | A | 37 | a0001c0001t0002g0001a0001c0001t0002g0042a0001c0001t0002g0043others(34): Show | 38 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(35): Show |
intron_variant | MODIFIER | c.66+2015G>A | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 2/7 | chr8 | 65672033 | ||||||
| chr8:65672330
|
T | C | 1 | a0001c0001t0001g0313 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.66+2312T>C | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 2/7 | chr8 | 65672330 | ||||||
| chr8:65672515
|
C | CT | 36 | a0001c0001t0002g0001a0001c0001t0002g0042a0001c0001t0002g0043others(33): Show | 37 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(34): Show |
intron_variant | MODIFIER | c.66+2508dupT | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr8 | 65672515 | |||||
| chr8:65673311
|
T | C | 79 | a0001c0001t0001g0071a0001c0001t0001g0072a0001c0001t0001g0073others(76): Show | 79 | HG00408.hp2 HG00438.hp1 HG00438.hp2 others(76): Show |
intron_variant | MODIFIER | c.66+3293T>C | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 2/7 | chr8 | 65673311 | ||||||
| chr8:65673331
|
C | T | 1 | a0001c0001t0001g0166 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.66+3313C>T | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 2/7 | chr8 | 65673331 | ||||||
| chr8:65673605
|
T | TA | 88 | a0001c0001t0001g0071a0001c0001t0001g0072a0001c0001t0001g0073others(85): Show | 88 | HG00408.hp2 HG00438.hp1 HG00438.hp2 others(85): Show |
intron_variant | MODIFIER | c.66+3601dupA | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr8 | 65673605 | |||||
| chr8:65673675
|
G | T | 1 | a0001c0001t0001g0201 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.66+3657G>T | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 2/7 | chr8 | 65673675 | ||||||
| chr8:65673846
|
C | G | 4 | a0001c0001t0001g0071a0001c0001t0001g0072a0001c0001t0001g0073others(1): Show | 4 | HG02559.hp2 HG02622.hp2 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.66+3828C>G | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 2/7 | chr8 | 65673846 | ||||||
| chr8:65673920
|
A | G | 1 | a0001c0001t0001g0310 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.66+3902A>G | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 2/7 | chr8 | 65673920 | ||||||
| chr8:65673926
|
T | C | 1 | a0001c0001t0001g0295 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.66+3908T>C | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 2/7 | chr8 | 65673926 | ||||||
| chr8:65674212
|
C | T | 3 | a0001c0001t0001g0085a0001c0001t0001g0086a0001c0001t0001g0087 | 3 | HG02257.hp2 HG03098.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.66+4194C>T | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 2/7 | chr8 | 65674212 | ||||||
| chr8:65674228
|
C | A | 1 | a0001c0001t0001g0072 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.66+4210C>A | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 2/7 | chr8 | 65674228 | ||||||
| chr8:65674261
|
A | C | 2 | a0001c0001t0005g0018a0001c0001t0005g0019 | 2 | NA18906.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.66+4243A>C | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 2/7 | chr8 | 65674261 | ||||||
| chr8:65674303
|
CT | C | 10 | a0001c0001t0001g0153a0001c0001t0001g0167a0001c0001t0001g0170others(7): Show | 10 | HG01167.hp1 HG01167.hp2 HG01256.hp2 others(7): Show |
intron_variant | MODIFIER | c.66+4301delT | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr8 | 65674303 | |||||
| chr8:65674320
|
A | T | 19 | a0001c0001t0003g0016a0001c0001t0003g0022a0001c0001t0003g0023others(16): Show | 19 | HG00140.hp1 HG00642.hp2 HG01346.hp1 others(16): Show |
intron_variant | MODIFIER | c.66+4302A>T | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 2/7 | chr8 | 65674320 | ||||||
| chr8:65674440
|
G | A | 1 | a0001c0001t0001g0102 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.66+4422G>A | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 2/7 | chr8 | 65674440 | ||||||
| chr8:65675177
|
G | A | 1 | a0001c0001t0001g0224 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.66+5159G>A | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 2/7 | chr8 | 65675177 | ||||||
| chr8:65675185
|
G | A | 2 | a0001c0001t0001g0108a0001c0001t0001g0277 | 2 | HG04115.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.66+5167G>A | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 2/7 | chr8 | 65675185 | ||||||
| chr8:65675207
|
G | A | 6 | a0001c0001t0005g0014a0001c0001t0005g0015a0001c0001t0005g0018others(3): Show | 6 | HG02647.hp2 HG02965.hp1 HG03540.hp1 others(3): Show |
intron_variant | MODIFIER | c.66+5189G>A | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 2/7 | chr8 | 65675207 | ||||||
| chr8:65675261
|
CCAGCCTG others(2): Show |
C | 3 | a0001c0001t0006g0340a0001c0001t0006g0341a0001c0001t0006g0342 | 3 | HG00733.hp1 HG01074.hp1 HG04204.hp1 |
intron_variant | MODIFIER | c.66+5245_66+5253del others(9): Show |
MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr8 | 65675261 | |||||
| chr8:65675288
|
G | A | 1 | a0001c0001t0001g0287 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.66+5270G>A | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 2/7 | chr8 | 65675288 | ||||||
| chr8:65675322
|
G | A | 1 | a0001c0001t0005g0020 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.66+5304G>A | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 2/7 | chr8 | 65675322 | ||||||
| chr8:65675549
|
A | G | 1 | a0001c0001t0001g0260 | 1 | HG01258.hp1 | intron_variant | MODIFIER | c.66+5531A>G | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 2/7 | chr8 | 65675549 | ||||||
| chr8:65675933
|
C | G | 32 | a0001c0001t0002g0001a0001c0001t0002g0039a0001c0001t0002g0042others(29): Show | 33 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(30): Show |
intron_variant | MODIFIER | c.66+5915C>G | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 2/7 | chr8 | 65675933 | ||||||
| chr8:65676230
|
A | C | 4 | a0001c0001t0002g0039a0001c0001t0002g0049a0001c0001t0002g0050others(1): Show | 4 | HG00140.hp2 HG01516.hp2 HG02602.hp2 others(1): Show |
intron_variant | MODIFIER | c.67-6123A>C | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 2/7 | chr8 | 65676230 | ||||||
| chr8:65676425
|
G | A | 3 | a0001c0001t0001g0101a0001c0001t0001g0141a0001c0001t0001g0229 | 3 | HG01167.hp1 HG02109.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.67-5928G>A | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 2/7 | chr8 | 65676425 | ||||||
| chr8:65676457
|
G | A | 1 | a0001c0001t0002g0039 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.67-5896G>A | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 2/7 | chr8 | 65676457 | ||||||
| chr8:65676458
|
G | T | 1 | a0001c0001t0004g0135 | 1 | NA18980.hp2 | intron_variant | MODIFIER | c.67-5895G>T | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 2/7 | chr8 | 65676458 | ||||||
| chr8:65676463
|
A | G | 5 | a0001c0001t0001g0071a0001c0001t0001g0072a0001c0001t0001g0073others(2): Show | 5 | HG02559.hp2 HG02622.hp2 HG02970.hp1 others(2): Show |
intron_variant | MODIFIER | c.67-5890A>G | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 2/7 | chr8 | 65676463 | ||||||
| chr8:65676520
|
C | T | 2 | a0001c0001t0001g0086a0001c0001t0001g0087 | 2 | HG03098.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.67-5833C>T | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 2/7 | chr8 | 65676520 | ||||||
| chr8:65676697
|
A | T | 4 | a0001c0001t0001g0288a0001c0001t0001g0317a0001c0001t0001g0319others(1): Show | 4 | HG00639.hp1 HG01123.hp1 HG01256.hp1 others(1): Show |
intron_variant | MODIFIER | c.67-5656A>T | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 2/7 | chr8 | 65676697 | ||||||
| chr8:65676978
|
G | A | 35 | a0001c0001t0001g0005a0001c0001t0001g0223a0001c0001t0001g0260others(32): Show | 36 | HG00099.hp2 HG00323.hp2 HG00639.hp1 others(33): Show |
intron_variant | MODIFIER | c.67-5375G>A | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 2/7 | chr8 | 65676978 | ||||||
| chr8:65676980
|
GCA | G | 3 | a0001c0001t0006g0340a0001c0001t0006g0341a0001c0001t0006g0342 | 3 | HG00733.hp1 HG01074.hp1 HG04204.hp1 |
intron_variant | MODIFIER | c.67-5360_67-5359del others(2): Show |
MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr8 | 65676980 | |||||
| chr8:65676985
|
C | T | 2 | a0001c0001t0002g0044a0001c0001t0002g0045 | 2 | HG00323.hp1 HG01175.hp2 |
intron_variant | MODIFIER | c.67-5368C>T | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 2/7 | chr8 | 65676985 | ||||||
| chr8:65677068
|
C | CT | 69 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008others(66): Show | 69 | HG00280.hp1 HG00438.hp1 HG00621.hp1 others(66): Show |
intron_variant | MODIFIER | c.67-5262dupT | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr8 | 65677068 | |||||
| chr8:65677068
|
C | CTT | 7 | a0001c0001t0001g0251a0001c0001t0001g0276a0001c0001t0001g0291others(4): Show | 7 | HG00733.hp1 HG01074.hp1 HG01192.hp2 others(4): Show |
intron_variant | MODIFIER | c.67-5263_67-5262dup others(2): Show |
MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr8 | 65677068 | |||||
| chr8:65677068
|
CT | C | 29 | a0001c0001t0001g0176a0001c0001t0001g0282a0001c0001t0001g0285others(26): Show | 30 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(27): Show |
intron_variant | MODIFIER | c.67-5262delT | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr8 | 65677068 | |||||
| chr8:65677103
|
T | C | 1 | a0001c0001t0003g0040 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.67-5250T>C | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 2/7 | chr8 | 65677103 | ||||||
| chr8:65677104
|
C | T | 1 | a0001c0001t0001g0110 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.67-5249C>T | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 2/7 | chr8 | 65677104 | ||||||
| chr8:65677105
|
G | A | 4 | a0001c0001t0001g0121a0001c0001t0001g0124a0001c0001t0001g0196others(1): Show | 4 | HG00438.hp1 NA18944.hp1 NA18956.hp2 others(1): Show |
intron_variant | MODIFIER | c.67-5248G>A | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 2/7 | chr8 | 65677105 | ||||||
| chr8:65677215
|
G | A | 1 | a0001c0001t0008g0013 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.67-5138G>A | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 2/7 | chr8 | 65677215 | ||||||
| chr8:65677278
|
C | G | 4 | a0001c0001t0001g0164a0001c0001t0001g0165a0001c0001t0001g0169others(1): Show | 4 | HG02040.hp1 NA18612.hp1 NA18946.hp2 others(1): Show |
intron_variant | MODIFIER | c.67-5075C>G | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 2/7 | chr8 | 65677278 | ||||||
| chr8:65677338
|
G | A | 1 | a0001c0001t0001g0111 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.67-5015G>A | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 2/7 | chr8 | 65677338 | ||||||
| chr8:65677384
|
C | CT | 86 | a0001c0001t0001g0071a0001c0001t0001g0072a0001c0001t0001g0073others(83): Show | 86 | HG00408.hp2 HG00438.hp1 HG00438.hp2 others(83): Show |
intron_variant | MODIFIER | c.67-4951dupT | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr8 | 65677384 | |||||
| chr8:65677386
|
T | C | 1 | a0001c0001t0001g0085 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.67-4967T>C | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 2/7 | chr8 | 65677386 | ||||||
| chr8:65677408
|
G | A | 1 | a0001c0001t0001g0298 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.67-4945G>A | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 2/7 | chr8 | 65677408 | ||||||
| chr8:65677409
|
G | A | 21 | a0001c0001t0003g0016a0001c0001t0003g0022a0001c0001t0003g0023others(18): Show | 21 | HG00140.hp1 HG00642.hp2 HG01168.hp2 others(18): Show |
intron_variant | MODIFIER | c.67-4944G>A | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 2/7 | chr8 | 65677409 | ||||||
| chr8:65677536
|
C | T | 2 | a0001c0001t0001g0235a0001c0001t0001g0292 | 2 | HG01884.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.67-4817C>T | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 2/7 | chr8 | 65677536 | ||||||
| chr8:65677845
|
G | A | 32 | a0001c0001t0002g0001a0001c0001t0002g0039a0001c0001t0002g0042others(29): Show | 33 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(30): Show |
intron_variant | MODIFIER | c.67-4508G>A | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 2/7 | chr8 | 65677845 | ||||||
| chr8:65678014
|
C | CA | 13 | a0001c0001t0001g0168a0001c0001t0001g0189a0001c0001t0001g0234others(10): Show | 13 | HG00733.hp1 HG01074.hp1 HG01123.hp2 others(10): Show |
intron_variant | MODIFIER | c.67-4322dupA | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr8 | 65678014 | |||||
| chr8:65678235
|
C | T | 1 | a0001c0001t0001g0339 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.67-4118C>T | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 2/7 | chr8 | 65678235 | ||||||
| chr8:65678244
|
C | A | 35 | a0001c0001t0001g0005a0001c0001t0001g0223a0001c0001t0001g0260others(32): Show | 36 | HG00099.hp2 HG00323.hp2 HG00639.hp1 others(33): Show |
intron_variant | MODIFIER | c.67-4109C>A | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 2/7 | chr8 | 65678244 | ||||||
| chr8:65678570
|
A | G | 62 | a0001c0001t0002g0001a0001c0001t0002g0039a0001c0001t0002g0042others(59): Show | 63 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(60): Show |
intron_variant | MODIFIER | c.67-3783A>G | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 2/7 | chr8 | 65678570 | ||||||
| chr8:65678594
|
A | T | 11 | a0001c0001t0001g0183a0001c0001t0001g0224a0001c0001t0001g0225others(8): Show | 11 | HG01109.hp1 HG02630.hp2 HG02896.hp1 others(8): Show |
intron_variant | MODIFIER | c.67-3759A>T | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 2/7 | chr8 | 65678594 | ||||||
| chr8:65678665
|
C | T | 1 | a0001c0001t0001g0225 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.67-3688C>T | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 2/7 | chr8 | 65678665 | ||||||
| chr8:65678815
|
A | G | 65 | a0001c0001t0002g0001a0001c0001t0002g0039a0001c0001t0002g0042others(62): Show | 66 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(63): Show |
intron_variant | MODIFIER | c.67-3538A>G | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 2/7 | chr8 | 65678815 | ||||||
| chr8:65678894
|
A | T | 3 | a0001c0001t0008g0011a0001c0001t0008g0012a0001c0001t0008g0013 | 3 | HG02486.hp1 HG03130.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.67-3459A>T | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 2/7 | chr8 | 65678894 | ||||||
| chr8:65679003
|
G | A | 35 | a0001c0001t0001g0005a0001c0001t0001g0223a0001c0001t0001g0260others(32): Show | 36 | HG00099.hp2 HG00323.hp2 HG00639.hp1 others(33): Show |
intron_variant | MODIFIER | c.67-3350G>A | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 2/7 | chr8 | 65679003 | ||||||
| chr8:65679060
|
T | C | 1 | a0001c0001t0001g0131 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.67-3293T>C | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 2/7 | chr8 | 65679060 | ||||||
| chr8:65679094
|
C | T | 21 | a0001c0001t0003g0016a0001c0001t0003g0022a0001c0001t0003g0023others(18): Show | 21 | HG00140.hp1 HG00642.hp2 HG01168.hp2 others(18): Show |
intron_variant | MODIFIER | c.67-3259C>T | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 2/7 | chr8 | 65679094 | ||||||
| chr8:65679103
|
A | C | 62 | a0001c0001t0002g0001a0001c0001t0002g0039a0001c0001t0002g0042others(59): Show | 63 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(60): Show |
intron_variant | MODIFIER | c.67-3250A>C | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 2/7 | chr8 | 65679103 | ||||||
| chr8:65679185
|
A | G | 2 | a0001c0001t0001g0162a0001c0001t0001g0213 | 2 | NA18960.hp2 NA18986.hp1 |
intron_variant | MODIFIER | c.67-3168A>G | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 2/7 | chr8 | 65679185 | ||||||
| chr8:65679234
|
T | C | 13 | a0001c0001t0001g0142a0001c0001t0001g0207a0001c0001t0001g0216others(10): Show | 13 | NA18955.hp1 NA18959.hp2 NA18965.hp1 others(10): Show |
intron_variant | MODIFIER | c.67-3119T>C | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 2/7 | chr8 | 65679234 | ||||||
| chr8:65679307
|
T | G | 1 | a0001c0001t0001g0319 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.67-3046T>G | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 2/7 | chr8 | 65679307 | ||||||
| chr8:65679435
|
G | A | 1 | a0001c0001t0001g0172 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.67-2918G>A | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 2/7 | chr8 | 65679435 | ||||||
| chr8:65679604
|
G | A | 1 | a0001c0001t0001g0149 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.67-2749G>A | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 2/7 | chr8 | 65679604 | ||||||
| chr8:65679862
|
T | C | 32 | a0001c0001t0002g0001a0001c0001t0002g0039a0001c0001t0002g0042others(29): Show | 33 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(30): Show |
intron_variant | MODIFIER | c.67-2491T>C | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 2/7 | chr8 | 65679862 | ||||||
| chr8:65679868
|
G | C | 62 | a0001c0001t0002g0001a0001c0001t0002g0039a0001c0001t0002g0042others(59): Show | 63 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(60): Show |
intron_variant | MODIFIER | c.67-2485G>C | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 2/7 | chr8 | 65679868 | ||||||
| chr8:65679937
|
C | A | 21 | a0001c0001t0003g0016a0001c0001t0003g0022a0001c0001t0003g0023others(18): Show | 21 | HG00140.hp1 HG00642.hp2 HG01168.hp2 others(18): Show |
intron_variant | MODIFIER | c.67-2416C>A | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 2/7 | chr8 | 65679937 | ||||||
| chr8:65679960
|
C | A | 21 | a0001c0001t0003g0016a0001c0001t0003g0022a0001c0001t0003g0023others(18): Show | 21 | HG00140.hp1 HG00642.hp2 HG01168.hp2 others(18): Show |
intron_variant | MODIFIER | c.67-2393C>A | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 2/7 | chr8 | 65679960 | ||||||
| chr8:65680173
|
G | T | 1 | a0001c0001t0001g0102 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.67-2180G>T | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 2/7 | chr8 | 65680173 | ||||||
| chr8:65680184
|
G | T | 1 | a0001c0001t0001g0282 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.67-2169G>T | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 2/7 | chr8 | 65680184 | ||||||
| chr8:65680310
|
G | C | 22 | a0001c0001t0001g0222a0001c0001t0001g0249a0001c0001t0001g0250others(19): Show | 22 | HG01070.hp2 HG01071.hp1 HG01192.hp2 others(19): Show |
intron_variant | MODIFIER | c.67-2043G>C | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 2/7 | chr8 | 65680310 | ||||||
| chr8:65680323
|
T | A | 22 | a0001c0001t0001g0222a0001c0001t0001g0249a0001c0001t0001g0250others(19): Show | 22 | HG01070.hp2 HG01071.hp1 HG01192.hp2 others(19): Show |
intron_variant | MODIFIER | c.67-2030T>A | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 2/7 | chr8 | 65680323 | ||||||
| chr8:65680627
|
G | A | 9 | a0001c0001t0005g0014a0001c0001t0005g0015a0001c0001t0005g0018others(6): Show | 9 | HG02486.hp1 HG02647.hp2 HG02965.hp1 others(6): Show |
intron_variant | MODIFIER | c.67-1726G>A | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 2/7 | chr8 | 65680627 | ||||||
| chr8:65680690
|
G | A | 3 | a0001c0001t0006g0340a0001c0001t0006g0341a0001c0001t0006g0342 | 3 | HG00733.hp1 HG01074.hp1 HG04204.hp1 |
intron_variant | MODIFIER | c.67-1663G>A | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 2/7 | chr8 | 65680690 | ||||||
| chr8:65680740
|
A | G | 6 | a0001c0001t0005g0014a0001c0001t0005g0015a0001c0001t0005g0018others(3): Show | 6 | HG02647.hp2 HG02965.hp1 HG03540.hp1 others(3): Show |
intron_variant | MODIFIER | c.67-1613A>G | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 2/7 | chr8 | 65680740 | ||||||
| chr8:65680853
|
C | G | 65 | a0001c0001t0002g0001a0001c0001t0002g0039a0001c0001t0002g0042others(62): Show | 66 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(63): Show |
intron_variant | MODIFIER | c.67-1500C>G | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 2/7 | chr8 | 65680853 | ||||||
| chr8:65680899
|
C | CT | 112 | a0001c0001t0001g0002a0001c0001t0001g0071a0001c0001t0001g0072others(109): Show | 113 | HG00438.hp1 HG00438.hp2 HG00544.hp1 others(110): Show |
intron_variant | MODIFIER | c.67-1430dupT | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr8 | 65680899 | |||||
| chr8:65680899
|
C | CTT | 8 | a0001c0001t0001g0085a0001c0001t0001g0108a0001c0001t0001g0112others(5): Show | 8 | HG00621.hp2 HG01934.hp1 HG02055.hp2 others(5): Show |
intron_variant | MODIFIER | c.67-1431_67-1430dup others(2): Show |
MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr8 | 65680899 | |||||
| chr8:65680899
|
CTTTT | C | 19 | a0001c0001t0003g0016a0001c0001t0003g0022a0001c0001t0003g0023others(16): Show | 19 | HG00140.hp1 HG00642.hp2 HG01168.hp2 others(16): Show |
intron_variant | MODIFIER | c.67-1433_67-1430del others(4): Show |
MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr8 | 65680899 | |||||
| chr8:65680899
|
CTTTTTTT others(3): Show |
C | 1 | a0001c0001t0001g0109 | 1 | NA19091.hp2 | intron_variant | MODIFIER | c.67-1439_67-1430del others(10): Show |
MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr8 | 65680899 | |||||
| chr8:65680948
|
C | G | 2 | a0001c0001t0002g0068a0001c0001t0002g0069 | 2 | HG02109.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.67-1405C>G | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 2/7 | chr8 | 65680948 | ||||||
| chr8:65681014
|
G | A | 5 | a0001c0001t0001g0251a0001c0001t0001g0255a0001c0001t0001g0262others(2): Show | 5 | HG01192.hp2 HG01884.hp2 HG01891.hp2 others(2): Show |
intron_variant | MODIFIER | c.67-1339G>A | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 2/7 | chr8 | 65681014 | ||||||
| chr8:65681157
|
C | G | 5 | a0001c0001t0001g0085a0001c0001t0001g0086a0001c0001t0001g0087others(2): Show | 5 | HG01243.hp2 HG02257.hp2 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.67-1196C>G | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 2/7 | chr8 | 65681157 | ||||||
| chr8:65681261
|
A | G | 1 | a0001c0001t0001g0165 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.67-1092A>G | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 2/7 | chr8 | 65681261 | ||||||
| chr8:65681592
|
A | G | 3 | a0001c0001t0006g0340a0001c0001t0006g0341a0001c0001t0006g0342 | 3 | HG00733.hp1 HG01074.hp1 HG04204.hp1 |
intron_variant | MODIFIER | c.67-761A>G | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 2/7 | chr8 | 65681592 | ||||||
| chr8:65681671
|
G | GT | 63 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008others(60): Show | 64 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(61): Show |
intron_variant | MODIFIER | c.67-666dupT | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr8 | 65681671 | |||||
| chr8:65681671
|
G | GTT | 15 | a0001c0001t0001g0009a0001c0001t0001g0100a0001c0001t0001g0172others(12): Show | 15 | HG00140.hp2 HG00735.hp1 HG01070.hp2 others(12): Show |
intron_variant | MODIFIER | c.67-667_67-666dupTT | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr8 | 65681671 | |||||
| chr8:65681677
|
T | G | 1 | a0001c0001t0001g0154 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.67-676T>G | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 2/7 | chr8 | 65681677 | ||||||
| chr8:65681814
|
A | G | 1 | a0001c0001t0001g0141 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.67-539A>G | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 2/7 | chr8 | 65681814 | ||||||
| chr8:65682049
|
TATGAAAA others(4): Show |
T | 1 | a0001c0001t0001g0287 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.67-296_67-286delCC others(9): Show |
MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr8 | 65682049 | |||||
| chr8:65682185
|
A | G | 1 | a0001c0001t0008g0013 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.67-168A>G | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 2/7 | chr8 | 65682185 | ||||||
| chr8:65682314
|
A | C | 1 | a0001c0001t0009g0117 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.67-39A>C | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 2/7 | chr8 | 65682314 | ||||||
| chr8:65682555
|
A | G | 19 | a0001c0001t0001g0002a0001c0001t0001g0094a0001c0001t0001g0095others(16): Show | 20 | HG01167.hp1 HG02027.hp1 HG02055.hp2 others(17): Show |
intron_variant | MODIFIER | c.165+104A>G | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 3/7 | chr8 | 65682555 | ||||||
| chr8:65682577
|
T | C | 2 | a0001c0001t0001g0252a0001c0001t0001g0253 | 2 | HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.165+126T>C | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 3/7 | chr8 | 65682577 | ||||||
| chr8:65682972
|
T | C | 1 | a0001c0001t0001g0075 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.165+521T>C | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 3/7 | chr8 | 65682972 | ||||||
| chr8:65683120
|
G | C | 1 | a0001c0001t0001g0230 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.165+669G>C | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 3/7 | chr8 | 65683120 | ||||||
| chr8:65683132
|
C | CT | 13 | a0001c0001t0001g0175a0001c0001t0001g0189a0001c0001t0001g0234others(10): Show | 13 | HG01069.hp1 HG01243.hp1 HG01243.hp2 others(10): Show |
intron_variant | MODIFIER | c.165+700dupT | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr8 | 65683132 | |||||
| chr8:65683132
|
CT | C | 66 | a0001c0001t0001g0101a0001c0001t0001g0222a0001c0001t0001g0229others(63): Show | 67 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(64): Show |
intron_variant | MODIFIER | c.165+700delT | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr8 | 65683132 | |||||
| chr8:65683412
|
G | A | 3 | a0001c0001t0006g0340a0001c0001t0006g0341a0001c0001t0006g0342 | 3 | HG00733.hp1 HG01074.hp1 HG04204.hp1 |
intron_variant | MODIFIER | c.165+961G>A | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 3/7 | chr8 | 65683412 | ||||||
| chr8:65683534
|
T | C | 6 | a0001c0001t0001g0207a0001c0001t0001g0216a0001c0001t0001g0218others(3): Show | 6 | NA18959.hp2 NA18979.hp1 NA18989.hp1 others(3): Show |
intron_variant | MODIFIER | c.165+1083T>C | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 3/7 | chr8 | 65683534 | ||||||
| chr8:65683608
|
G | T | 32 | a0001c0001t0002g0001a0001c0001t0002g0039a0001c0001t0002g0042others(29): Show | 33 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(30): Show |
intron_variant | MODIFIER | c.165+1157G>T | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 3/7 | chr8 | 65683608 | ||||||
| chr8:65683727
|
T | G | 32 | a0001c0001t0002g0001a0001c0001t0002g0039a0001c0001t0002g0042others(29): Show | 33 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(30): Show |
intron_variant | MODIFIER | c.165+1276T>G | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 3/7 | chr8 | 65683727 | ||||||
| chr8:65683776
|
C | T | 3 | a0001c0001t0001g0164a0001c0001t0001g0165a0001c0001t0001g0169 | 3 | HG02040.hp1 NA18612.hp1 NA18980.hp1 |
intron_variant | MODIFIER | c.165+1325C>T | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 3/7 | chr8 | 65683776 | ||||||
| chr8:65683992
|
A | G | 1 | a0001c0001t0001g0160 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.165+1541A>G | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 3/7 | chr8 | 65683992 | ||||||
| chr8:65684059
|
G | A | 3 | a0001c0001t0006g0340a0001c0001t0006g0341a0001c0001t0006g0342 | 3 | HG00733.hp1 HG01074.hp1 HG04204.hp1 |
intron_variant | MODIFIER | c.165+1608G>A | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 3/7 | chr8 | 65684059 | ||||||
| chr8:65684060
|
T | A | 1 | a0001c0001t0001g0182 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.165+1609T>A | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 3/7 | chr8 | 65684060 | ||||||
| chr8:65684083
|
G | A | 1 | a0001c0001t0002g0042 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.165+1632G>A | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 3/7 | chr8 | 65684083 | ||||||
| chr8:65684085
|
A | G | 65 | a0001c0001t0002g0001a0001c0001t0002g0039a0001c0001t0002g0042others(62): Show | 66 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(63): Show |
intron_variant | MODIFIER | c.165+1634A>G | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 3/7 | chr8 | 65684085 | ||||||
| chr8:65684629
|
T | C | 1 | a0001c0001t0001g0101 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.165+2178T>C | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 3/7 | chr8 | 65684629 | ||||||
| chr8:65684802
|
C | T | 6 | a0001c0001t0005g0014a0001c0001t0005g0015a0001c0001t0005g0018others(3): Show | 6 | HG02647.hp2 HG02965.hp1 HG03540.hp1 others(3): Show |
intron_variant | MODIFIER | c.165+2351C>T | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 3/7 | chr8 | 65684802 | ||||||
| chr8:65684879
|
CT | C | 3 | a0001c0001t0001g0085a0001c0001t0001g0086a0001c0001t0001g0087 | 3 | HG02257.hp2 HG03098.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.165+2429delT | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 3/7 | chr8 | 65684879 | ||||||
| chr8:65685034
|
T | G | 10 | a0001c0001t0001g0293a0001c0001t0001g0294a0001c0001t0001g0295others(7): Show | 10 | HG01070.hp2 HG01071.hp1 HG02258.hp1 others(7): Show |
intron_variant | MODIFIER | c.165+2583T>G | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 3/7 | chr8 | 65685034 | ||||||
| chr8:65685107
|
T | C | 67 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(64): Show | 68 | HG00099.hp2 HG00323.hp2 HG00639.hp1 others(65): Show |
intron_variant | MODIFIER | c.165+2656T>C | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 3/7 | chr8 | 65685107 | ||||||
| chr8:65685247
|
T | C | 2 | a0001c0001t0001g0128a0001c0001t0001g0129 | 2 | NA18951.hp2 NA18977.hp1 |
intron_variant | MODIFIER | c.165+2796T>C | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 3/7 | chr8 | 65685247 | ||||||
| chr8:65685470
|
C | T | 1 | a0001c0001t0001g0150 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.165+3019C>T | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 3/7 | chr8 | 65685470 | ||||||
| chr8:65685671
|
G | A | 1 | a0001c0001t0001g0208 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.165+3220G>A | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 3/7 | chr8 | 65685671 | ||||||
| chr8:65685679
|
G | A | 1 | a0001c0001t0002g0049 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.165+3228G>A | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 3/7 | chr8 | 65685679 | ||||||
| chr8:65685796
|
A | G | 1 | a0001c0001t0002g0060 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.165+3345A>G | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 3/7 | chr8 | 65685796 | ||||||
| chr8:65685890
|
C | A | 1 | a0001c0001t0001g0108 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.165+3439C>A | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 3/7 | chr8 | 65685890 | ||||||
| chr8:65685969
|
G | A | 21 | a0001c0001t0003g0016a0001c0001t0003g0022a0001c0001t0003g0023others(18): Show | 21 | HG00140.hp1 HG00642.hp2 HG01168.hp2 others(18): Show |
intron_variant | MODIFIER | c.165+3518G>A | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 3/7 | chr8 | 65685969 | ||||||
| chr8:65686022
|
A | G | 1 | a0001c0001t0001g0164 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.165+3571A>G | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 3/7 | chr8 | 65686022 | ||||||
| chr8:65686146
|
T | C | 1 | a0001c0001t0001g0169 | 1 | NA18980.hp1 | intron_variant | MODIFIER | c.165+3695T>C | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 3/7 | chr8 | 65686146 | ||||||
| chr8:65686253
|
C | T | 1 | a0001c0001t0001g0175 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.165+3802C>T | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 3/7 | chr8 | 65686253 | ||||||
| chr8:65686348
|
G | T | 1 | a0001c0001t0001g0185 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.165+3897G>T | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 3/7 | chr8 | 65686348 | ||||||
| chr8:65686400
|
C | T | 22 | a0001c0001t0001g0222a0001c0001t0001g0249a0001c0001t0001g0250others(19): Show | 22 | HG01070.hp2 HG01071.hp1 HG01192.hp2 others(19): Show |
intron_variant | MODIFIER | c.165+3949C>T | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 3/7 | chr8 | 65686400 | ||||||
| chr8:65686457
|
A | G | 1 | a0001c0001t0001g0234 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.165+4006A>G | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 3/7 | chr8 | 65686457 | ||||||
| chr8:65686463
|
T | G | 5 | a0001c0001t0001g0251a0001c0001t0001g0255a0001c0001t0001g0262others(2): Show | 5 | HG01192.hp2 HG01884.hp2 HG01891.hp2 others(2): Show |
intron_variant | MODIFIER | c.165+4012T>G | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 3/7 | chr8 | 65686463 | ||||||
| chr8:65686579
|
C | CA | 21 | a0001c0001t0001g0009a0001c0001t0001g0091a0001c0001t0001g0108others(18): Show | 21 | HG00280.hp1 HG01192.hp2 HG01243.hp2 others(18): Show |
intron_variant | MODIFIER | c.165+4149dupA | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr8 | 65686579 | |||||
| chr8:65686579
|
CA | C | 68 | a0001c0001t0001g0212a0001c0001t0001g0246a0001c0001t0001g0252others(65): Show | 69 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(66): Show |
intron_variant | MODIFIER | c.165+4149delA | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr8 | 65686579 | |||||
| chr8:65686597
|
A | C | 1 | a0001c0001t0003g0030 | 1 | NA19001.hp1 | intron_variant | MODIFIER | c.165+4146A>C | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 3/7 | chr8 | 65686597 | ||||||
| chr8:65686600
|
A | G | 1 | a0001c0001t0001g0238 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.165+4149A>G | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 3/7 | chr8 | 65686600 | ||||||
| chr8:65686845
|
A | T | 1 | a0001c0001t0001g0279 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.165+4394A>T | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 3/7 | chr8 | 65686845 | ||||||
| chr8:65686845
|
AC | A | 6 | a0001c0001t0005g0014a0001c0001t0005g0015a0001c0001t0005g0018others(3): Show | 6 | HG02647.hp2 HG02965.hp1 HG03540.hp1 others(3): Show |
intron_variant | MODIFIER | c.165+4397delC | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr8 | 65686845 | |||||
| chr8:65686848
|
C | G | 2 | a0001c0001t0001g0252a0001c0001t0001g0253 | 2 | HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.165+4397C>G | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 3/7 | chr8 | 65686848 | ||||||
| chr8:65687114
|
C | G | 342 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(339): Show | 347 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(344): Show |
intron_variant | MODIFIER | c.165+4663C>G | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 3/7 | chr8 | 65687114 | ||||||
| chr8:65687347
|
CT | C | 246 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0006others(243): Show | 249 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(246): Show |
intron_variant | MODIFIER | c.165+4913delT | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr8 | 65687347 | |||||
| chr8:65687835
|
C | A | 1 | a0001c0001t0001g0183 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.165+5384C>A | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 3/7 | chr8 | 65687835 | ||||||
| chr8:65687970
|
C | T | 3 | a0001c0001t0006g0340a0001c0001t0006g0341a0001c0001t0006g0342 | 3 | HG00733.hp1 HG01074.hp1 HG04204.hp1 |
intron_variant | MODIFIER | c.165+5519C>T | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 3/7 | chr8 | 65687970 | ||||||
| chr8:65687981
|
T | A | 1 | a0001c0001t0001g0287 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.165+5530T>A | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 3/7 | chr8 | 65687981 | ||||||
| chr8:65687998
|
A | G | 309 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(306): Show | 314 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(311): Show |
intron_variant | MODIFIER | c.165+5547A>G | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 3/7 | chr8 | 65687998 | ||||||
| chr8:65688000
|
T | C | 9 | a0001c0001t0005g0014a0001c0001t0005g0015a0001c0001t0005g0018others(6): Show | 9 | HG02486.hp1 HG02647.hp2 HG02965.hp1 others(6): Show |
intron_variant | MODIFIER | c.165+5549T>C | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 3/7 | chr8 | 65688000 | ||||||
| chr8:65688027
|
G | A | 1 | a0001c0001t0001g0260 | 1 | HG01258.hp1 | intron_variant | MODIFIER | c.165+5576G>A | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 3/7 | chr8 | 65688027 | ||||||
| chr8:65688059
|
C | G | 1 | a0001c0001t0008g0013 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.166-5585C>G | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 3/7 | chr8 | 65688059 | ||||||
| chr8:65688098
|
T | TA | 92 | a0001c0001t0001g0006a0001c0001t0001g0009a0001c0001t0001g0075others(89): Show | 92 | HG00280.hp1 HG00408.hp1 HG00408.hp2 others(89): Show |
intron_variant | MODIFIER | c.166-5528dupA | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr8 | 65688098 | |||||
| chr8:65688098
|
T | TAA | 7 | a0001c0001t0001g0072a0001c0001t0001g0073a0001c0001t0001g0074others(4): Show | 7 | HG01074.hp1 HG02622.hp2 HG03209.hp1 others(4): Show |
intron_variant | MODIFIER | c.166-5529_166-5528d others(4): Show |
MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr8 | 65688098 | |||||
| chr8:65688098
|
T | TAAAAA | 18 | a0001c0001t0003g0016a0001c0001t0003g0022a0001c0001t0003g0023others(15): Show | 18 | HG00140.hp1 HG01168.hp2 HG01346.hp1 others(15): Show |
intron_variant | MODIFIER | c.166-5532_166-5528d others(7): Show |
MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr8 | 65688098 | |||||
| chr8:65688098
|
TA | T | 33 | a0001c0001t0001g0005a0001c0001t0001g0223a0001c0001t0001g0260others(30): Show | 34 | HG00099.hp2 HG00323.hp2 HG00639.hp1 others(31): Show |
intron_variant | MODIFIER | c.166-5528delA | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr8 | 65688098 | |||||
| chr8:65688118
|
A | C | 8 | a0001c0001t0001g0293a0001c0001t0001g0295a0001c0001t0001g0296others(5): Show | 8 | HG01070.hp2 HG01071.hp1 HG02280.hp2 others(5): Show |
intron_variant | MODIFIER | c.166-5526A>C | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 3/7 | chr8 | 65688118 | ||||||
| chr8:65688230
|
A | G | 35 | a0001c0001t0001g0005a0001c0001t0001g0223a0001c0001t0001g0260others(32): Show | 36 | HG00099.hp2 HG00323.hp2 HG00639.hp1 others(33): Show |
intron_variant | MODIFIER | c.166-5414A>G | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 3/7 | chr8 | 65688230 | ||||||
| chr8:65688405
|
A | G | 2 | a0001c0001t0001g0089a0001c0001t0001g0152 | 2 | NA18945.hp2 NA19003.hp2 |
intron_variant | MODIFIER | c.166-5239A>G | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 3/7 | chr8 | 65688405 | ||||||
| chr8:65688451
|
C | CT | 108 | a0001c0001t0001g0071a0001c0001t0001g0072a0001c0001t0001g0073others(105): Show | 109 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(106): Show |
intron_variant | MODIFIER | c.166-5178dupT | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr8 | 65688451 | |||||
| chr8:65688451
|
C | CTT | 17 | a0001c0001t0001g0002a0001c0001t0001g0094a0001c0001t0001g0096others(14): Show | 18 | HG01167.hp1 HG02027.hp1 HG02055.hp2 others(15): Show |
intron_variant | MODIFIER | c.166-5179_166-5178d others(4): Show |
MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr8 | 65688451 | |||||
| chr8:65688456
|
T | C | 9 | a0001c0001t0005g0014a0001c0001t0005g0015a0001c0001t0005g0018others(6): Show | 9 | HG02486.hp1 HG02647.hp2 HG02965.hp1 others(6): Show |
intron_variant | MODIFIER | c.166-5188T>C | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 3/7 | chr8 | 65688456 | ||||||
| chr8:65688472
|
G | A | 1 | a0001c0001t0001g0127 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.166-5172G>A | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 3/7 | chr8 | 65688472 | ||||||
| chr8:65688512
|
A | T | 1 | a0001c0001t0001g0147 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.166-5132A>T | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 3/7 | chr8 | 65688512 | ||||||
| chr8:65688675
|
A | G | 3 | a0001c0001t0006g0340a0001c0001t0006g0341a0001c0001t0006g0342 | 3 | HG00733.hp1 HG01074.hp1 HG04204.hp1 |
intron_variant | MODIFIER | c.166-4969A>G | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 3/7 | chr8 | 65688675 | ||||||
| chr8:65688719
|
A | G | 3 | a0001c0001t0001g0074a0001c0001t0001g0113a0001c0001t0001g0147 | 3 | HG02027.hp2 NA18970.hp1 NA18987.hp1 |
intron_variant | MODIFIER | c.166-4925A>G | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 3/7 | chr8 | 65688719 | ||||||
| chr8:65688725
|
G | A | 5 | a0001c0001t0001g0260a0001c0001t0001g0322a0001c0001t0001g0329others(2): Show | 5 | HG00738.hp2 HG01070.hp1 HG01258.hp1 others(2): Show |
intron_variant | MODIFIER | c.166-4919G>A | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 3/7 | chr8 | 65688725 | ||||||
| chr8:65688916
|
G | A | 1 | a0001c0001t0001g0123 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.166-4728G>A | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 3/7 | chr8 | 65688916 | ||||||
| chr8:65689102
|
G | A | 3 | a0001c0001t0006g0340a0001c0001t0006g0341a0001c0001t0006g0342 | 3 | HG00733.hp1 HG01074.hp1 HG04204.hp1 |
intron_variant | MODIFIER | c.166-4542G>A | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 3/7 | chr8 | 65689102 | ||||||
| chr8:65689200
|
G | T | 2 | a0001c0001t0001g0252a0001c0001t0001g0253 | 2 | HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.166-4444G>T | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 3/7 | chr8 | 65689200 | ||||||
| chr8:65689334
|
C | G | 1 | a0001c0001t0001g0074 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.166-4310C>G | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 3/7 | chr8 | 65689334 | ||||||
| chr8:65689434
|
G | A | 9 | a0001c0001t0005g0014a0001c0001t0005g0015a0001c0001t0005g0018others(6): Show | 9 | HG02486.hp1 HG02647.hp2 HG02965.hp1 others(6): Show |
intron_variant | MODIFIER | c.166-4210G>A | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 3/7 | chr8 | 65689434 | ||||||
| chr8:65689546
|
T | C | 1 | a0001c0001t0001g0230 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.166-4098T>C | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 3/7 | chr8 | 65689546 | ||||||
| chr8:65689812
|
AAAG | A | 9 | a0001c0001t0005g0014a0001c0001t0005g0015a0001c0001t0005g0018others(6): Show | 9 | HG02486.hp1 HG02647.hp2 HG02965.hp1 others(6): Show |
intron_variant | MODIFIER | c.166-3827_166-3825d others(5): Show |
MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr8 | 65689812 | |||||
| chr8:65690111
|
CAT | C | 20 | a0001c0001t0001g0002a0001c0001t0001g0094a0001c0001t0001g0095others(17): Show | 21 | HG01167.hp1 HG02027.hp1 HG02055.hp2 others(18): Show |
intron_variant | MODIFIER | c.166-3530_166-3529d others(4): Show |
MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr8 | 65690111 | |||||
| chr8:65690278
|
T | C | 1 | a0001c0001t0001g0230 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.166-3366T>C | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 3/7 | chr8 | 65690278 | ||||||
| chr8:65690367
|
T | C | 3 | a0001c0001t0006g0340a0001c0001t0006g0341a0001c0001t0006g0342 | 3 | HG00733.hp1 HG01074.hp1 HG04204.hp1 |
intron_variant | MODIFIER | c.166-3277T>C | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 3/7 | chr8 | 65690367 | ||||||
| chr8:65690374
|
C | T | 43 | a0001c0001t0001g0005a0001c0001t0001g0189a0001c0001t0001g0223others(40): Show | 44 | HG00099.hp2 HG00323.hp2 HG00639.hp1 others(41): Show |
intron_variant | MODIFIER | c.166-3270C>T | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 3/7 | chr8 | 65690374 | ||||||
| chr8:65690461
|
G | A | 9 | a0001c0001t0005g0014a0001c0001t0005g0015a0001c0001t0005g0018others(6): Show | 9 | HG02486.hp1 HG02647.hp2 HG02965.hp1 others(6): Show |
intron_variant | MODIFIER | c.166-3183G>A | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 3/7 | chr8 | 65690461 | ||||||
| chr8:65690551
|
T | C | 3 | a0001c0001t0006g0340a0001c0001t0006g0341a0001c0001t0006g0342 | 3 | HG00733.hp1 HG01074.hp1 HG04204.hp1 |
intron_variant | MODIFIER | c.166-3093T>C | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 3/7 | chr8 | 65690551 | ||||||
| chr8:65690560
|
G | GT | 71 | a0001c0001t0001g0074a0001c0001t0001g0075a0001c0001t0001g0079others(68): Show | 71 | HG00408.hp1 HG00408.hp2 HG00438.hp1 others(68): Show |
intron_variant | MODIFIER | c.166-3077dupT | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr8 | 65690560 | |||||
| chr8:65690599
|
C | T | 12 | a0001c0001t0001g0222a0001c0001t0001g0249a0001c0001t0001g0250others(9): Show | 12 | HG01192.hp2 HG01884.hp2 HG01891.hp2 others(9): Show |
intron_variant | MODIFIER | c.166-3045C>T | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 3/7 | chr8 | 65690599 | ||||||
| chr8:65690626
|
A | G | 9 | a0001c0001t0005g0014a0001c0001t0005g0015a0001c0001t0005g0018others(6): Show | 9 | HG02486.hp1 HG02647.hp2 HG02965.hp1 others(6): Show |
intron_variant | MODIFIER | c.166-3018A>G | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 3/7 | chr8 | 65690626 | ||||||
| chr8:65690735
|
T | C | 2 | a0001c0001t0001g0101a0001c0001t0001g0229 | 2 | HG01167.hp1 HG02109.hp1 |
intron_variant | MODIFIER | c.166-2909T>C | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 3/7 | chr8 | 65690735 | ||||||
| chr8:65690837
|
C | T | 1 | a0001c0001t0001g0277 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.166-2807C>T | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 3/7 | chr8 | 65690837 | ||||||
| chr8:65691362
|
A | G | 2 | a0001c0001t0001g0190a0001c0001t0001g0208 | 2 | HG01496.hp1 NA19084.hp1 |
intron_variant | MODIFIER | c.166-2282A>G | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 3/7 | chr8 | 65691362 | ||||||
| chr8:65691505
|
C | T | 3 | a0001c0001t0006g0340a0001c0001t0006g0341a0001c0001t0006g0342 | 3 | HG00733.hp1 HG01074.hp1 HG04204.hp1 |
intron_variant | MODIFIER | c.166-2139C>T | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 3/7 | chr8 | 65691505 | ||||||
| chr8:65691640
|
A | G | 3 | a0001c0001t0006g0340a0001c0001t0006g0341a0001c0001t0006g0342 | 3 | HG00733.hp1 HG01074.hp1 HG04204.hp1 |
intron_variant | MODIFIER | c.166-2004A>G | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 3/7 | chr8 | 65691640 | ||||||
| chr8:65691658
|
G | GT | 8 | a0001c0001t0001g0096a0001c0001t0001g0188a0001c0001t0001g0216others(5): Show | 8 | HG01123.hp1 HG01346.hp1 HG01934.hp1 others(5): Show |
intron_variant | MODIFIER | c.166-1977dupT | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr8 | 65691658 | |||||
| chr8:65691725
|
C | T | 13 | a0001c0001t0001g0142a0001c0001t0001g0207a0001c0001t0001g0216others(10): Show | 13 | NA18955.hp1 NA18959.hp2 NA18965.hp1 others(10): Show |
intron_variant | MODIFIER | c.166-1919C>T | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 3/7 | chr8 | 65691725 | ||||||
| chr8:65692012
|
T | A | 1 | a0001c0001t0001g0215 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.166-1632T>A | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 3/7 | chr8 | 65692012 | ||||||
| chr8:65692347
|
T | A | 2 | a0001c0001t0001g0251a0001c0001t0001g0255 | 2 | HG01192.hp2 HG02145.hp2 |
intron_variant | MODIFIER | c.166-1297T>A | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 3/7 | chr8 | 65692347 | ||||||
| chr8:65692355
|
T | C | 45 | a0001c0001t0001g0005a0001c0001t0001g0173a0001c0001t0001g0174others(42): Show | 46 | HG00099.hp2 HG00323.hp2 HG00639.hp1 others(43): Show |
intron_variant | MODIFIER | c.166-1289T>C | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 3/7 | chr8 | 65692355 | ||||||
| chr8:65692423
|
C | T | 1 | a0001c0001t0001g0005 | 2 | HG03490.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.166-1221C>T | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 3/7 | chr8 | 65692423 | ||||||
| chr8:65692716
|
CTGTT | C | 8 | a0001c0001t0001g0002a0001c0001t0001g0094a0001c0001t0001g0096others(5): Show | 9 | NA18957.hp2 NA18970.hp2 NA18971.hp1 others(6): Show |
intron_variant | MODIFIER | c.166-923_166-920del others(4): Show |
MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr8 | 65692716 | |||||
| chr8:65692793
|
T | A | 32 | a0001c0001t0002g0001a0001c0001t0002g0039a0001c0001t0002g0042others(29): Show | 33 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(30): Show |
intron_variant | MODIFIER | c.166-851T>A | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 3/7 | chr8 | 65692793 | ||||||
| chr8:65692892
|
C | CT | 8 | a0001c0001t0001g0108a0001c0001t0001g0151a0001c0001t0001g0226others(5): Show | 8 | HG01258.hp1 HG01261.hp1 HG01346.hp2 others(5): Show |
intron_variant | MODIFIER | c.166-737dupT | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr8 | 65692892 | |||||
| chr8:65692966
|
G | C | 1 | a0001c0001t0001g0100 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.166-678G>C | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 3/7 | chr8 | 65692966 | ||||||
| chr8:65693104
|
T | A | 1 | a0001c0001t0001g0149 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.166-540T>A | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 3/7 | chr8 | 65693104 | ||||||
| chr8:65693256
|
C | T | 8 | a0001c0001t0001g0002a0001c0001t0001g0094a0001c0001t0001g0096others(5): Show | 9 | NA18957.hp2 NA18970.hp2 NA18971.hp1 others(6): Show |
intron_variant | MODIFIER | c.166-388C>T | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 3/7 | chr8 | 65693256 | ||||||
| chr8:65693315
|
C | T | 1 | a0001c0001t0004g0202 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.166-329C>T | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 3/7 | chr8 | 65693315 | ||||||
| chr8:65693316
|
G | A | 62 | a0001c0001t0002g0001a0001c0001t0002g0039a0001c0001t0002g0042others(59): Show | 63 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(60): Show |
intron_variant | MODIFIER | c.166-328G>A | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 3/7 | chr8 | 65693316 | ||||||
| chr8:65693356
|
AG | A | 5 | a0001c0001t0001g0085a0001c0001t0001g0086a0001c0001t0001g0087others(2): Show | 5 | HG01243.hp2 HG02257.hp2 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.166-287delG | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 3/7 | chr8 | 65693356 | ||||||
| chr8:65693401
|
C | CA | 10 | a0001c0001t0001g0179a0001c0001t0002g0043a0001c0001t0002g0047others(7): Show | 10 | HG00733.hp1 HG00735.hp1 HG00741.hp1 others(7): Show |
intron_variant | MODIFIER | c.166-230dupA | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr8 | 65693401 | |||||
| chr8:65693401
|
C | T | 1 | a0001c0001t0001g0175 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.166-243C>T | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 3/7 | chr8 | 65693401 | ||||||
| chr8:65693533
|
A | G | 2 | a0001c0001t0001g0257a0001c0001t0001g0258 | 2 | HG01243.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.166-111A>G | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 3/7 | chr8 | 65693533 | ||||||
| chr8:65693629
|
A | G | 10 | a0001c0001t0001g0293a0001c0001t0001g0294a0001c0001t0001g0295others(7): Show | 10 | HG01070.hp2 HG01071.hp1 HG02258.hp1 others(7): Show |
intron_variant | MODIFIER | c.166-15A>G | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 3/7 | chr8 | 65693629 | ||||||
| chr8:65693827
|
G | T | 2 | a0001c0001t0001g0257a0001c0001t0001g0258 | 2 | HG01243.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.281+68G>T | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 4/7 | chr8 | 65693827 | ||||||
| chr8:65693924
|
A | G | 1 | a0001c0001t0011g0070 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.281+165A>G | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 4/7 | chr8 | 65693924 | ||||||
| chr8:65694072
|
C | CT | 73 | a0001c0001t0001g0087a0001c0001t0001g0092a0001c0001t0001g0094others(70): Show | 74 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(71): Show |
intron_variant | MODIFIER | c.281+334dupT | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr8 | 65694072 | |||||
| chr8:65694072
|
CT | C | 27 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008others(24): Show | 27 | HG01109.hp1 HG01255.hp2 HG01258.hp1 others(24): Show |
intron_variant | MODIFIER | c.281+334delT | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr8 | 65694072 | |||||
| chr8:65694184
|
C | T | 1 | a0001c0001t0001g0291 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.281+425C>T | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 4/7 | chr8 | 65694184 | ||||||
| chr8:65694321
|
C | T | 2 | a0001c0001t0001g0321a0001c0001t0001g0334 | 2 | HG01081.hp1 HG01106.hp1 |
intron_variant | MODIFIER | c.281+562C>T | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 4/7 | chr8 | 65694321 | ||||||
| chr8:65694434
|
G | A | 3 | a0001c0001t0006g0340a0001c0001t0006g0341a0001c0001t0006g0342 | 3 | HG00733.hp1 HG01074.hp1 HG04204.hp1 |
intron_variant | MODIFIER | c.281+675G>A | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 4/7 | chr8 | 65694434 | ||||||
| chr8:65694534
|
C | T | 1 | a0001c0001t0001g0230 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.281+775C>T | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 4/7 | chr8 | 65694534 | ||||||
| chr8:65694765
|
A | C | 1 | a0001c0001t0001g0309 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.281+1006A>C | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 4/7 | chr8 | 65694765 | ||||||
| chr8:65694984
|
G | A | 92 | a0001c0001t0001g0085a0001c0001t0001g0086a0001c0001t0001g0087others(89): Show | 93 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(90): Show |
intron_variant | MODIFIER | c.281+1225G>A | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 4/7 | chr8 | 65694984 | ||||||
| chr8:65695006
|
A | C | 1 | a0001c0001t0006g0340 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.281+1247A>C | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 4/7 | chr8 | 65695006 | ||||||
| chr8:65695059
|
T | C | 4 | a0001c0001t0001g0101a0001c0001t0001g0141a0001c0001t0001g0229others(1): Show | 4 | HG01167.hp1 HG02109.hp1 HG03516.hp1 others(1): Show |
intron_variant | MODIFIER | c.281+1300T>C | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 4/7 | chr8 | 65695059 | ||||||
| chr8:65695209
|
G | A | 10 | a0001c0001t0001g0293a0001c0001t0001g0294a0001c0001t0001g0295others(7): Show | 10 | HG01070.hp2 HG01071.hp1 HG02258.hp1 others(7): Show |
intron_variant | MODIFIER | c.281+1450G>A | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 4/7 | chr8 | 65695209 | ||||||
| chr8:65695312
|
T | C | 9 | a0001c0001t0005g0014a0001c0001t0005g0015a0001c0001t0005g0018others(6): Show | 9 | HG02486.hp1 HG02647.hp2 HG02965.hp1 others(6): Show |
intron_variant | MODIFIER | c.281+1553T>C | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 4/7 | chr8 | 65695312 | ||||||
| chr8:65695347
|
A | AT | 31 | a0001c0001t0002g0001a0001c0001t0002g0039a0001c0001t0002g0042others(28): Show | 32 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(29): Show |
intron_variant | MODIFIER | c.281+1599dupT | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr8 | 65695347 | |||||
| chr8:65695495
|
T | G | 1 | a0001c0001t0001g0111 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.281+1736T>G | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 4/7 | chr8 | 65695495 | ||||||
| chr8:65695532
|
T | C | 2 | a0001c0001t0001g0257a0001c0001t0001g0258 | 2 | HG01243.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.281+1773T>C | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 4/7 | chr8 | 65695532 | ||||||
| chr8:65695830
|
T | A | 1 | a0001c0001t0001g0194 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.281+2071T>A | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 4/7 | chr8 | 65695830 | ||||||
| chr8:65695867
|
A | G | 1 | a0001c0001t0001g0242 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.281+2108A>G | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 4/7 | chr8 | 65695867 | ||||||
| chr8:65695874
|
G | A | 27 | a0001c0001t0001g0142a0001c0001t0001g0151a0001c0001t0001g0153others(24): Show | 27 | HG01123.hp2 HG01256.hp2 HG01258.hp2 others(24): Show |
intron_variant | MODIFIER | c.281+2115G>A | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 4/7 | chr8 | 65695874 | ||||||
| chr8:65695970
|
A | G | 5 | a0001c0001t0001g0071a0001c0001t0001g0072a0001c0001t0001g0073others(2): Show | 5 | HG02559.hp2 HG02622.hp2 HG02970.hp1 others(2): Show |
intron_variant | MODIFIER | c.281+2211A>G | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 4/7 | chr8 | 65695970 | ||||||
| chr8:65696265
|
C | G | 23 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008others(20): Show | 23 | HG01109.hp1 HG01255.hp2 HG01433.hp2 others(20): Show |
intron_variant | MODIFIER | c.281+2506C>G | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 4/7 | chr8 | 65696265 | ||||||
| chr8:65696413
|
C | T | 2 | a0001c0001t0001g0271a0001c0001t0001g0272 | 2 | HG02486.hp2 HG02809.hp1 |
intron_variant | MODIFIER | c.281+2654C>T | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 4/7 | chr8 | 65696413 | ||||||
| chr8:65696618
|
C | T | 1 | a0001c0001t0001g0143 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.281+2859C>T | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 4/7 | chr8 | 65696618 | ||||||
| chr8:65696716
|
G | A | 1 | a0001c0001t0001g0224 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.281+2957G>A | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 4/7 | chr8 | 65696716 | ||||||
| chr8:65696746
|
C | T | 3 | a0001c0001t0001g0085a0001c0001t0001g0086a0001c0001t0001g0087 | 3 | HG02257.hp2 HG03098.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.281+2987C>T | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 4/7 | chr8 | 65696746 | ||||||
| chr8:65696824
|
C | G | 1 | a0001c0001t0001g0151 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.281+3065C>G | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 4/7 | chr8 | 65696824 | ||||||
| chr8:65696829
|
T | C | 1 | a0001c0001t0001g0339 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.281+3070T>C | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 4/7 | chr8 | 65696829 | ||||||
| chr8:65696912
|
C | T | 1 | a0001c0001t0001g0141 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.281+3153C>T | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 4/7 | chr8 | 65696912 | ||||||
| chr8:65696938
|
A | G | 3 | a0001c0001t0006g0340a0001c0001t0006g0341a0001c0001t0006g0342 | 3 | HG00733.hp1 HG01074.hp1 HG04204.hp1 |
intron_variant | MODIFIER | c.281+3179A>G | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 4/7 | chr8 | 65696938 | ||||||
| chr8:65696984
|
C | CT | 130 | a0001c0001t0001g0002a0001c0001t0001g0071a0001c0001t0001g0072others(127): Show | 131 | HG00140.hp1 HG00408.hp2 HG00438.hp1 others(128): Show |
intron_variant | MODIFIER | c.281+3243dupT | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr8 | 65696984 | |||||
| chr8:65697096
|
T | C | 3 | a0001c0001t0006g0340a0001c0001t0006g0341a0001c0001t0006g0342 | 3 | HG00733.hp1 HG01074.hp1 HG04204.hp1 |
intron_variant | MODIFIER | c.281+3337T>C | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 4/7 | chr8 | 65697096 | ||||||
| chr8:65697129
|
C | T | 3 | a0001c0001t0001g0268a0001c0001t0001g0308a0001c0001t0001g0309 | 3 | HG02451.hp2 HG02809.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.281+3370C>T | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 4/7 | chr8 | 65697129 | ||||||
| chr8:65697156
|
T | C | 23 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008others(20): Show | 23 | HG01109.hp1 HG01255.hp2 HG01433.hp2 others(20): Show |
intron_variant | MODIFIER | c.281+3397T>C | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 4/7 | chr8 | 65697156 | ||||||
| chr8:65697286
|
A | T | 1 | a0001c0001t0001g0182 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.281+3527A>T | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 4/7 | chr8 | 65697286 | ||||||
| chr8:65697314
|
A | G | 65 | a0001c0001t0002g0001a0001c0001t0002g0039a0001c0001t0002g0042others(62): Show | 66 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(63): Show |
intron_variant | MODIFIER | c.281+3555A>G | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 4/7 | chr8 | 65697314 | ||||||
| chr8:65697341
|
C | T | 1 | a0001c0001t0001g0180 | 1 | NA18993.hp2 | intron_variant | MODIFIER | c.281+3582C>T | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 4/7 | chr8 | 65697341 | ||||||
| chr8:65697707
|
G | A | 1 | a0001c0001t0002g0054 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.281+3948G>A | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 4/7 | chr8 | 65697707 | ||||||
| chr8:65697740
|
G | A | 3 | a0001c0001t0006g0340a0001c0001t0006g0341a0001c0001t0006g0342 | 3 | HG00733.hp1 HG01074.hp1 HG04204.hp1 |
intron_variant | MODIFIER | c.281+3981G>A | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 4/7 | chr8 | 65697740 | ||||||
| chr8:65697750
|
A | G | 9 | a0001c0001t0005g0014a0001c0001t0005g0015a0001c0001t0005g0018others(6): Show | 9 | HG02486.hp1 HG02647.hp2 HG02965.hp1 others(6): Show |
intron_variant | MODIFIER | c.281+3991A>G | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 4/7 | chr8 | 65697750 | ||||||
| chr8:65697788
|
A | T | 1 | a0001c0001t0001g0141 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.281+4029A>T | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 4/7 | chr8 | 65697788 | ||||||
| chr8:65697839
|
C | T | 1 | a0001c0001t0001g0279 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.281+4080C>T | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 4/7 | chr8 | 65697839 | ||||||
| chr8:65697999
|
G | A | 1 | a0001c0001t0001g0238 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.281+4240G>A | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 4/7 | chr8 | 65697999 | ||||||
| chr8:65698115
|
G | A | 1 | a0001c0001t0001g0203 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.281+4356G>A | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 4/7 | chr8 | 65698115 | ||||||
| chr8:65698142
|
A | T | 5 | a0001c0001t0005g0015a0001c0001t0005g0018a0001c0001t0005g0019others(2): Show | 5 | HG02965.hp1 HG03540.hp1 HG06807.hp2 others(2): Show |
intron_variant | MODIFIER | c.281+4383A>T | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 4/7 | chr8 | 65698142 | ||||||
| chr8:65698154
|
C | CT | 65 | a0001c0001t0001g0074a0001c0001t0001g0075a0001c0001t0001g0080others(62): Show | 65 | HG00408.hp2 HG00438.hp1 HG00438.hp2 others(62): Show |
intron_variant | MODIFIER | c.281+4408dupT | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr8 | 65698154 | |||||
| chr8:65698251
|
C | A | 2 | a0001c0001t0001g0257a0001c0001t0001g0258 | 2 | HG01243.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.281+4492C>A | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 4/7 | chr8 | 65698251 | ||||||
| chr8:65698253
|
A | G | 5 | a0001c0001t0001g0085a0001c0001t0001g0086a0001c0001t0001g0087others(2): Show | 5 | HG01243.hp2 HG02257.hp2 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.281+4494A>G | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 4/7 | chr8 | 65698253 | ||||||
| chr8:65698382
|
C | T | 32 | a0001c0001t0002g0001a0001c0001t0002g0039a0001c0001t0002g0042others(29): Show | 33 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(30): Show |
intron_variant | MODIFIER | c.281+4623C>T | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 4/7 | chr8 | 65698382 | ||||||
| chr8:65698491
|
C | A | 3 | a0001c0001t0001g0085a0001c0001t0001g0086a0001c0001t0001g0087 | 3 | HG02257.hp2 HG03098.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.281+4732C>A | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 4/7 | chr8 | 65698491 | ||||||
| chr8:65698571
|
G | A | 100 | a0001c0001t0001g0085a0001c0001t0001g0086a0001c0001t0001g0087others(97): Show | 101 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(98): Show |
intron_variant | MODIFIER | c.281+4812G>A | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 4/7 | chr8 | 65698571 | ||||||
| chr8:65698594
|
A | G | 1 | a0001c0001t0001g0287 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.281+4835A>G | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 4/7 | chr8 | 65698594 | ||||||
| chr8:65698732
|
C | CT | 30 | a0001c0001t0001g0189a0001c0001t0001g0222a0001c0001t0001g0234others(27): Show | 30 | HG01070.hp2 HG01071.hp1 HG01192.hp2 others(27): Show |
intron_variant | MODIFIER | c.281+4986dupT | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr8 | 65698732 | |||||
| chr8:65698792
|
G | A | 1 | a0001c0001t0001g0075 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.281+5033G>A | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 4/7 | chr8 | 65698792 | ||||||
| chr8:65698885
|
C | T | 1 | a0001c0001t0001g0302 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.281+5126C>T | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 4/7 | chr8 | 65698885 | ||||||
| chr8:65698965
|
G | A | 6 | a0001c0001t0005g0014a0001c0001t0005g0015a0001c0001t0005g0018others(3): Show | 6 | HG02647.hp2 HG02965.hp1 HG03540.hp1 others(3): Show |
intron_variant | MODIFIER | c.281+5206G>A | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 4/7 | chr8 | 65698965 | ||||||
| chr8:65699182
|
C | T | 92 | a0001c0001t0001g0085a0001c0001t0001g0086a0001c0001t0001g0087others(89): Show | 93 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(90): Show |
intron_variant | MODIFIER | c.281+5423C>T | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 4/7 | chr8 | 65699182 | ||||||
| chr8:65699307
|
G | A | 1 | a0001c0001t0001g0124 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.282-5387G>A | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 4/7 | chr8 | 65699307 | ||||||
| chr8:65699355
|
C | T | 8 | a0001c0001t0001g0002a0001c0001t0001g0094a0001c0001t0001g0096others(5): Show | 9 | NA18957.hp2 NA18970.hp2 NA18971.hp1 others(6): Show |
intron_variant | MODIFIER | c.282-5339C>T | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 4/7 | chr8 | 65699355 | ||||||
| chr8:65699381
|
A | G | 21 | a0001c0001t0003g0016a0001c0001t0003g0022a0001c0001t0003g0023others(18): Show | 21 | HG00140.hp1 HG00642.hp2 HG01168.hp2 others(18): Show |
intron_variant | MODIFIER | c.282-5313A>G | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 4/7 | chr8 | 65699381 | ||||||
| chr8:65699465
|
A | G | 2 | a0001c0001t0002g0047a0001c0001t0002g0048 | 2 | HG00741.hp1 HG01192.hp1 |
intron_variant | MODIFIER | c.282-5229A>G | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 4/7 | chr8 | 65699465 | ||||||
| chr8:65699467
|
A | C | 1 | a0001c0001t0004g0132 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.282-5227A>C | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 4/7 | chr8 | 65699467 | ||||||
| chr8:65699572
|
C | A | 21 | a0001c0001t0003g0016a0001c0001t0003g0022a0001c0001t0003g0023others(18): Show | 21 | HG00140.hp1 HG00642.hp2 HG01168.hp2 others(18): Show |
intron_variant | MODIFIER | c.282-5122C>A | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 4/7 | chr8 | 65699572 | ||||||
| chr8:65699749
|
C | G | 2 | a0001c0001t0001g0323a0001c0001t0001g0327 | 2 | HG00639.hp2 HG01934.hp2 |
intron_variant | MODIFIER | c.282-4945C>G | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 4/7 | chr8 | 65699749 | ||||||
| chr8:65699779
|
A | G | 9 | a0001c0001t0005g0014a0001c0001t0005g0015a0001c0001t0005g0018others(6): Show | 9 | HG02486.hp1 HG02647.hp2 HG02965.hp1 others(6): Show |
intron_variant | MODIFIER | c.282-4915A>G | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 4/7 | chr8 | 65699779 | ||||||
| chr8:65700175
|
A | G | 2 | a0001c0001t0001g0101a0001c0001t0001g0229 | 2 | HG01167.hp1 HG02109.hp1 |
intron_variant | MODIFIER | c.282-4519A>G | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 4/7 | chr8 | 65700175 | ||||||
| chr8:65700225
|
C | T | 1 | a0001c0001t0001g0178 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.282-4469C>T | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 4/7 | chr8 | 65700225 | ||||||
| chr8:65700272
|
G | A | 3 | a0001c0001t0006g0340a0001c0001t0006g0341a0001c0001t0006g0342 | 3 | HG00733.hp1 HG01074.hp1 HG04204.hp1 |
intron_variant | MODIFIER | c.282-4422G>A | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 4/7 | chr8 | 65700272 | ||||||
| chr8:65700335
|
A | G | 10 | a0001c0001t0001g0002a0001c0001t0001g0094a0001c0001t0001g0095others(7): Show | 11 | HG02027.hp1 NA18944.hp2 NA18957.hp2 others(8): Show |
intron_variant | MODIFIER | c.282-4359A>G | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 4/7 | chr8 | 65700335 | ||||||
| chr8:65700349
|
TA | T | 6 | a0001c0001t0001g0136a0001c0001t0001g0208a0001c0001t0001g0270others(3): Show | 6 | HG01070.hp1 HG01255.hp2 HG03041.hp2 others(3): Show |
intron_variant | MODIFIER | c.282-4328delA | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr8 | 65700349 | |||||
| chr8:65700366
|
AG | A | 12 | a0001c0001t0002g0042a0001c0001t0002g0063a0001c0001t0003g0016others(9): Show | 12 | HG00140.hp1 HG02647.hp2 HG02965.hp1 others(9): Show |
intron_variant | MODIFIER | c.282-4327delG | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 4/7 | chr8 | 65700366 | ||||||
| chr8:65700367
|
G | A | 52 | a0001c0001t0002g0001a0001c0001t0002g0039a0001c0001t0002g0043others(49): Show | 53 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(50): Show |
intron_variant | MODIFIER | c.282-4327G>A | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 4/7 | chr8 | 65700367 | ||||||
| chr8:65700369
|
A | G | 1 | a0001c0001t0011g0070 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.282-4325A>G | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 4/7 | chr8 | 65700369 | ||||||
| chr8:65700373
|
A | G | 19 | a0001c0001t0001g0002a0001c0001t0001g0094a0001c0001t0001g0095others(16): Show | 20 | HG01167.hp1 HG02027.hp1 HG02055.hp2 others(17): Show |
intron_variant | MODIFIER | c.282-4321A>G | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 4/7 | chr8 | 65700373 | ||||||
| chr8:65700451
|
G | A | 21 | a0001c0001t0003g0016a0001c0001t0003g0022a0001c0001t0003g0023others(18): Show | 21 | HG00140.hp1 HG00642.hp2 HG01168.hp2 others(18): Show |
intron_variant | MODIFIER | c.282-4243G>A | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 4/7 | chr8 | 65700451 | ||||||
| chr8:65700754
|
T | C | 37 | a0001c0001t0001g0005a0001c0001t0001g0173a0001c0001t0001g0174others(34): Show | 38 | HG00099.hp2 HG00323.hp2 HG00639.hp1 others(35): Show |
intron_variant | MODIFIER | c.282-3940T>C | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 4/7 | chr8 | 65700754 | ||||||
| chr8:65701032
|
G | A | 1 | a0001c0001t0001g0336 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.282-3662G>A | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 4/7 | chr8 | 65701032 | ||||||
| chr8:65701107
|
A | G | 1 | a0001c0001t0001g0238 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.282-3587A>G | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 4/7 | chr8 | 65701107 | ||||||
| chr8:65701289
|
G | A | 2 | a0001c0001t0002g0054a0001c0001t0002g0057 | 2 | HG00280.hp2 HG01255.hp1 |
intron_variant | MODIFIER | c.282-3405G>A | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 4/7 | chr8 | 65701289 | ||||||
| chr8:65701710
|
A | C | 1 | a0001c0001t0001g0337 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.282-2984A>C | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 4/7 | chr8 | 65701710 | ||||||
| chr8:65701726
|
A | G | 77 | a0001c0001t0001g0071a0001c0001t0001g0072a0001c0001t0001g0073others(74): Show | 77 | HG00408.hp2 HG00438.hp1 HG00438.hp2 others(74): Show |
intron_variant | MODIFIER | c.282-2968A>G | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 4/7 | chr8 | 65701726 | ||||||
| chr8:65702152
|
C | T | 5 | a0001c0001t0001g0071a0001c0001t0001g0072a0001c0001t0001g0073others(2): Show | 5 | HG02559.hp2 HG02622.hp2 HG02970.hp1 others(2): Show |
intron_variant | MODIFIER | c.282-2542C>T | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 4/7 | chr8 | 65702152 | ||||||
| chr8:65702263
|
TTTTCTTT others(6): Show |
T | 31 | a0001c0001t0002g0001a0001c0001t0002g0039a0001c0001t0002g0042others(28): Show | 32 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(29): Show |
intron_variant | MODIFIER | c.282-2418_282-2406d others(15): Show |
MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr8 | 65702263 | |||||
| chr8:65702297
|
CT | C | 94 | a0001c0001t0001g0002a0001c0001t0001g0071a0001c0001t0001g0072others(91): Show | 95 | HG00099.hp1 HG00408.hp2 HG00438.hp1 others(92): Show |
intron_variant | MODIFIER | c.282-2377delT | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr8 | 65702297 | |||||
| chr8:65702297
|
CTT | C | 24 | a0001c0001t0001g0222a0001c0001t0001g0249a0001c0001t0001g0250others(21): Show | 24 | HG01070.hp2 HG01071.hp1 HG01192.hp2 others(21): Show |
intron_variant | MODIFIER | c.282-2378_282-2377d others(4): Show |
MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr8 | 65702297 | |||||
| chr8:65702301
|
T | C | 1 | a0001c0001t0001g0226 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.282-2393T>C | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 4/7 | chr8 | 65702301 | ||||||
| chr8:65702302
|
T | C | 2 | a0001c0001t0001g0073a0001c0001t0001g0104 | 2 | HG02559.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.282-2392T>C | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 4/7 | chr8 | 65702302 | ||||||
| chr8:65702484
|
G | C | 32 | a0001c0001t0002g0001a0001c0001t0002g0039a0001c0001t0002g0042others(29): Show | 33 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(30): Show |
intron_variant | MODIFIER | c.282-2210G>C | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 4/7 | chr8 | 65702484 | ||||||
| chr8:65702560
|
C | A | 283 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0006others(280): Show | 286 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(283): Show |
intron_variant | MODIFIER | c.282-2134C>A | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 4/7 | chr8 | 65702560 | ||||||
| chr8:65702602
|
T | G | 1 | a0001c0001t0001g0148 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.282-2092T>G | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 4/7 | chr8 | 65702602 | ||||||
| chr8:65702704
|
G | A | 5 | a0001c0001t0001g0071a0001c0001t0001g0072a0001c0001t0001g0073others(2): Show | 5 | HG02559.hp2 HG02622.hp2 HG02970.hp1 others(2): Show |
intron_variant | MODIFIER | c.282-1990G>A | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 4/7 | chr8 | 65702704 | ||||||
| chr8:65702793
|
T | G | 1 | a0001c0001t0001g0251 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.282-1901T>G | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 4/7 | chr8 | 65702793 | ||||||
| chr8:65702823
|
A | AT | 65 | a0001c0001t0002g0001a0001c0001t0002g0039a0001c0001t0002g0042others(62): Show | 66 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(63): Show |
intron_variant | MODIFIER | c.282-1871_282-1870i others(3): Show |
MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 4/7 | chr8 | 65702823 | ||||||
| chr8:65702849
|
T | C | 4 | a0001c0001t0001g0004a0001c0001t0001g0161a0001c0001t0001g0167others(1): Show | 5 | HG00738.hp1 HG01167.hp2 HG01169.hp1 others(2): Show |
intron_variant | MODIFIER | c.282-1845T>C | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 4/7 | chr8 | 65702849 | ||||||
| chr8:65702908
|
A | G | 1 | a0001c0001t0001g0179 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.282-1786A>G | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 4/7 | chr8 | 65702908 | ||||||
| chr8:65703062
|
A | AGTTAACT others(8): Show |
1 | a0001c0001t0001g0231 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.282-1631_282-1617d others(17): Show |
MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr8 | 65703062 | |||||
| chr8:65703077
|
G | A | 1 | a0001c0001t0001g0268 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.282-1617G>A | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 4/7 | chr8 | 65703077 | ||||||
| chr8:65703090
|
G | GA | 6 | a0001c0001t0001g0254a0001c0001t0001g0266a0001c0001t0001g0296others(3): Show | 6 | HG00738.hp2 HG01255.hp2 HG01433.hp2 others(3): Show |
intron_variant | MODIFIER | c.282-1591dupA | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr8 | 65703090 | |||||
| chr8:65703235
|
A | G | 8 | a0001c0001t0001g0189a0001c0001t0001g0234a0001c0001t0001g0235others(5): Show | 8 | HG01243.hp1 HG01884.hp1 HG02559.hp1 others(5): Show |
intron_variant | MODIFIER | c.282-1459A>G | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 4/7 | chr8 | 65703235 | ||||||
| chr8:65703257
|
G | A | 1 | a0001c0001t0001g0339 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.282-1437G>A | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 4/7 | chr8 | 65703257 | ||||||
| chr8:65703380
|
T | C | 1 | a0001c0001t0001g0271 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.282-1314T>C | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 4/7 | chr8 | 65703380 | ||||||
| chr8:65703403
|
A | G | 1 | a0001c0001t0001g0309 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.282-1291A>G | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 4/7 | chr8 | 65703403 | ||||||
| chr8:65703419
|
G | GT | 47 | a0001c0001t0001g0005a0001c0001t0001g0009a0001c0001t0001g0090others(44): Show | 48 | HG00544.hp2 HG00639.hp1 HG00735.hp2 others(45): Show |
intron_variant | MODIFIER | c.282-1243dupT | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr8 | 65703419 | |||||
| chr8:65703419
|
G | GTT | 17 | a0001c0001t0001g0088a0001c0001t0001g0143a0001c0001t0001g0155others(14): Show | 17 | HG01106.hp1 HG01168.hp1 HG01175.hp1 others(14): Show |
intron_variant | MODIFIER | c.282-1244_282-1243d others(4): Show |
MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr8 | 65703419 | |||||
| chr8:65703419
|
G | GTTT | 14 | a0001c0001t0001g0148a0001c0001t0001g0189a0001c0001t0001g0223others(11): Show | 14 | HG00323.hp2 HG01169.hp2 HG01243.hp1 others(11): Show |
intron_variant | MODIFIER | c.282-1245_282-1243d others(5): Show |
MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr8 | 65703419 | |||||
| chr8:65703419
|
GT | G | 13 | a0001c0001t0001g0095a0001c0001t0001g0096a0001c0001t0001g0098others(10): Show | 13 | HG01346.hp1 HG02109.hp1 HG04115.hp2 others(10): Show |
intron_variant | MODIFIER | c.282-1243delT | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr8 | 65703419 | |||||
| chr8:65703419
|
GTT | G | 25 | a0001c0001t0001g0002a0001c0001t0001g0094a0001c0001t0001g0097others(22): Show | 26 | HG01099.hp2 HG01168.hp2 HG02027.hp1 others(23): Show |
intron_variant | MODIFIER | c.282-1244_282-1243d others(4): Show |
MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr8 | 65703419 | |||||
| chr8:65703419
|
GTTT | G | 33 | a0001c0001t0001g0072a0001c0001t0001g0107a0001c0001t0001g0108others(30): Show | 33 | HG00140.hp1 HG00438.hp1 HG00438.hp2 others(30): Show |
intron_variant | MODIFIER | c.282-1245_282-1243d others(5): Show |
MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr8 | 65703419 | |||||
| chr8:65703419
|
GTTTT | G | 84 | a0001c0001t0001g0071a0001c0001t0001g0073a0001c0001t0001g0074others(81): Show | 85 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(82): Show |
intron_variant | MODIFIER | c.282-1246_282-1243d others(6): Show |
MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr8 | 65703419 | |||||
| chr8:65703419
|
GTTTTT | G | 8 | a0001c0001t0002g0043a0001c0001t0005g0014a0001c0001t0005g0015others(5): Show | 8 | HG01943.hp1 HG02486.hp1 HG02647.hp2 others(5): Show |
intron_variant | MODIFIER | c.282-1247_282-1243d others(7): Show |
MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr8 | 65703419 | |||||
| chr8:65703419
|
GTTTTTTT others(4): Show |
G | 1 | a0001c0001t0001g0182 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.282-1253_282-1243d others(13): Show |
MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr8 | 65703419 | |||||
| chr8:65703419
|
GTTTTTTT others(5): Show |
G | 3 | a0001c0001t0001g0253a0001c0001t0001g0323a0001c0001t0001g0327 | 3 | HG00639.hp2 HG01934.hp2 HG02895.hp2 |
intron_variant | MODIFIER | c.282-1254_282-1243d others(14): Show |
MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr8 | 65703419 | |||||
| chr8:65703419
|
GTTTTTTT others(6): Show |
G | 1 | a0001c0001t0001g0252 | 1 | HG02897.hp2 | intron_variant | MODIFIER | c.282-1255_282-1243d others(15): Show |
MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr8 | 65703419 | |||||
| chr8:65703419
|
GTTTTTTT others(10): Show |
G | 1 | a0001c0001t0001g0255 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.282-1259_282-1243d others(19): Show |
MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr8 | 65703419 | |||||
| chr8:65703419
|
GTTTTTTT others(11): Show |
G | 4 | a0001c0001t0001g0251a0001c0001t0001g0262a0001c0001t0001g0303others(1): Show | 4 | HG01192.hp2 HG01884.hp2 HG01891.hp2 others(1): Show |
intron_variant | MODIFIER | c.282-1260_282-1243d others(20): Show |
MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr8 | 65703419 | |||||
| chr8:65703427
|
T | TTG | 9 | a0001c0001t0001g0293a0001c0001t0001g0294a0001c0001t0001g0295others(6): Show | 9 | HG01070.hp2 HG01071.hp1 HG02258.hp1 others(6): Show |
intron_variant | MODIFIER | c.282-1266_282-1265i others(4): Show |
MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr8 | 65703427 | |||||
| chr8:65703437
|
T | G | 3 | a0001c0001t0006g0340a0001c0001t0006g0341a0001c0001t0006g0342 | 3 | HG00733.hp1 HG01074.hp1 HG04204.hp1 |
intron_variant | MODIFIER | c.282-1257T>G | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 4/7 | chr8 | 65703437 | ||||||
| chr8:65703509
|
C | T | 9 | a0001c0001t0001g0005a0001c0001t0001g0288a0001c0001t0001g0315others(6): Show | 10 | HG00323.hp2 HG00639.hp1 HG01123.hp1 others(7): Show |
intron_variant | MODIFIER | c.282-1185C>T | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 4/7 | chr8 | 65703509 | ||||||
| chr8:65703622
|
C | G | 1 | a0001c0001t0001g0130 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.282-1072C>G | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 4/7 | chr8 | 65703622 | ||||||
| chr8:65703701
|
C | T | 6 | a0001c0001t0005g0014a0001c0001t0005g0015a0001c0001t0005g0018others(3): Show | 6 | HG02647.hp2 HG02965.hp1 HG03540.hp1 others(3): Show |
intron_variant | MODIFIER | c.282-993C>T | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 4/7 | chr8 | 65703701 | ||||||
| chr8:65703766
|
T | C | 71 | a0001c0001t0001g0074a0001c0001t0001g0075a0001c0001t0001g0079others(68): Show | 71 | HG00408.hp2 HG00438.hp1 HG00438.hp2 others(68): Show |
intron_variant | MODIFIER | c.282-928T>C | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 4/7 | chr8 | 65703766 | ||||||
| chr8:65703783
|
A | G | 1 | a0001c0001t0001g0307 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.282-911A>G | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 4/7 | chr8 | 65703783 | ||||||
| chr8:65703861
|
C | T | 1 | a0001c0001t0001g0277 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.282-833C>T | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 4/7 | chr8 | 65703861 | ||||||
| chr8:65703941
|
C | T | 1 | a0001c0001t0002g0059 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.282-753C>T | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 4/7 | chr8 | 65703941 | ||||||
| chr8:65704231
|
A | G | 1 | a0001c0001t0001g0100 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.282-463A>G | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 4/7 | chr8 | 65704231 | ||||||
| chr8:65704320
|
T | G | 1 | a0001c0001t0003g0022 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.282-374T>G | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 4/7 | chr8 | 65704320 | ||||||
| chr8:65704400
|
G | A | 1 | a0001c0001t0002g0059 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.282-294G>A | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 4/7 | chr8 | 65704400 | ||||||
| chr8:65704671
|
C | T | 1 | a0001c0001t0001g0203 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.282-23C>T | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 4/7 | chr8 | 65704671 | ||||||
| chr8:65705000
|
A | T | 1 | a0001c0001t0001g0277 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.517+71A>T | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 5/7 | chr8 | 65705000 | ||||||
| chr8:65705121
|
C | G | 3 | a0001c0001t0001g0085a0001c0001t0001g0086a0001c0001t0001g0087 | 3 | HG02257.hp2 HG03098.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.517+192C>G | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 5/7 | chr8 | 65705121 | ||||||
| chr8:65705149
|
C | G | 82 | a0001c0001t0001g0071a0001c0001t0001g0072a0001c0001t0001g0073others(79): Show | 82 | HG00408.hp2 HG00438.hp1 HG00438.hp2 others(79): Show |
intron_variant | MODIFIER | c.517+220C>G | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 5/7 | chr8 | 65705149 | ||||||
| chr8:65705301
|
C | T | 1 | a0001c0001t0001g0141 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.517+372C>T | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 5/7 | chr8 | 65705301 | ||||||
| chr8:65705302
|
G | A | 9 | a0001c0001t0005g0014a0001c0001t0005g0015a0001c0001t0005g0018others(6): Show | 9 | HG02486.hp1 HG02647.hp2 HG02965.hp1 others(6): Show |
intron_variant | MODIFIER | c.517+373G>A | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 5/7 | chr8 | 65705302 | ||||||
| chr8:65705355
|
G | T | 1 | a0001c0001t0001g0296 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.517+426G>T | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 5/7 | chr8 | 65705355 | ||||||
| chr8:65705430
|
C | A | 1 | a0001c0001t0001g0095 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.517+501C>A | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 5/7 | chr8 | 65705430 | ||||||
| chr8:65705627
|
G | A | 1 | a0001c0001t0001g0218 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.517+698G>A | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 5/7 | chr8 | 65705627 | ||||||
| chr8:65705690
|
C | G | 1 | a0001c0001t0001g0246 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.517+761C>G | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 5/7 | chr8 | 65705690 | ||||||
| chr8:65705918
|
G | A | 1 | a0001c0001t0001g0222 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.517+989G>A | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 5/7 | chr8 | 65705918 | ||||||
| chr8:65706192
|
T | G | 1 | a0001c0001t0001g0179 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.518-818T>G | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 5/7 | chr8 | 65706192 | ||||||
| chr8:65706268
|
A | ATAATTTT others(51): Show |
1 | a0001c0001t0001g0266 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.518-741_518-684dup others(58): Show |
MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr8 | 65706268 | |||||
| chr8:65706325
|
A | G | 8 | a0001c0001t0001g0189a0001c0001t0001g0234a0001c0001t0001g0235others(5): Show | 8 | HG01243.hp1 HG01884.hp1 HG02559.hp1 others(5): Show |
intron_variant | MODIFIER | c.518-685A>G | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 5/7 | chr8 | 65706325 | ||||||
| chr8:65706353
|
A | G | 5 | a0001c0001t0002g0051a0001c0001t0002g0053a0001c0001t0002g0056others(2): Show | 5 | NA18989.hp2 NA18997.hp1 NA19065.hp1 others(2): Show |
intron_variant | MODIFIER | c.518-657A>G | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 5/7 | chr8 | 65706353 | ||||||
| chr8:65706485
|
C | T | 2 | a0001c0001t0002g0068a0001c0001t0002g0069 | 2 | HG02109.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.518-525C>T | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 5/7 | chr8 | 65706485 | ||||||
| chr8:65706581
|
G | A | 2 | a0001c0001t0001g0180a0001c0001t0001g0181 | 2 | NA18993.hp2 NA19066.hp2 |
intron_variant | MODIFIER | c.518-429G>A | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 5/7 | chr8 | 65706581 | ||||||
| chr8:65707461
|
T | C | 1 | a0001c0001t0001g0179 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.764+205T>C | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 6/7 | chr8 | 65707461 | ||||||
| chr8:65707530
|
A | C | 1 | a0001c0001t0001g0215 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.764+274A>C | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 6/7 | chr8 | 65707530 | ||||||
| chr8:65707536
|
A | G | 15 | a0001c0001t0001g0002a0001c0001t0001g0094a0001c0001t0001g0095others(12): Show | 16 | HG02027.hp1 HG02055.hp2 HG02486.hp2 others(13): Show |
intron_variant | MODIFIER | c.764+280A>G | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 6/7 | chr8 | 65707536 | ||||||
| chr8:65707594
|
CTATTTGC others(50): Show |
C | 1 | a0001c0001t0001g0266 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.765-248_765-192del others(57): Show |
MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 6/7 | chr8 | 65707594 | ||||||
| chr8:65707659
|
T | C | 1 | a0001c0001t0001g0266 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.765-184T>C | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 6/7 | chr8 | 65707659 | ||||||
| chr8:65707664
|
T | A | 1 | a0001c0001t0001g0266 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.765-179T>A | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 6/7 | chr8 | 65707664 | ||||||
| chr8:65707748
|
G | A | 1 | a0001c0001t0001g0313 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.765-95G>A | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 6/7 | chr8 | 65707748 | ||||||
| chr8:65708061
|
T | A | 1 | a0001c0001t0001g0110 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.933+50T>A | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 7/7 | chr8 | 65708061 | ||||||
| chr8:65708124
|
G | A | 59 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(56): Show | 60 | HG00099.hp2 HG00323.hp2 HG00639.hp1 others(57): Show |
intron_variant | MODIFIER | c.933+113G>A | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 7/7 | chr8 | 65708124 | ||||||
| chr8:65708391
|
G | A | 1 | a0001c0001t0001g0123 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.933+380G>A | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 7/7 | chr8 | 65708391 | ||||||
| chr8:65708613
|
C | G | 1 | a0001c0001t0001g0322 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.934-363C>G | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 7/7 | chr8 | 65708613 | ||||||
| chr8:65708918
|
C | T | 3 | a0001c0001t0006g0340a0001c0001t0006g0341a0001c0001t0006g0342 | 3 | HG00733.hp1 HG01074.hp1 HG04204.hp1 |
intron_variant | MODIFIER | c.934-58C>T | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 7/7 | chr8 | 65708918 | ||||||
| chr8:65708919
|
G | A | 1 | a0001c0001t0001g0238 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.934-57G>A | MTFR1 | ENSG00000066855.16 | transcript | ENST00000262146.9 | protein_coding | 7/7 | chr8 | 65708919 |