Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 4242 |
| ensemblid | ENSG00000100060.18 |
| hgncid | 7038 |
| symbol | MFNG |
| name | MFNG O-fucosylpeptide 3-beta-N-acetylglucosaminyltransferase |
| refseq_nuc | NM_002405.4 |
| refseq_prot | NP_002396.2 |
| ensembl_nuc | ENST00000356998.8 |
| ensembl_prot | ENSP00000349490.3 |
| mane_status | MANE Select |
| chr | chr22 |
| start | 37469063 |
| end | 37486384 |
| strand | - |
| ver | v1.2 |
| region | chr22:37469063-37486384 |
| region5000 | chr22:37464063-37491384 |
| regionname0 | MFNG_chr22_37469063_37486384 |
| regionname5000 | MFNG_chr22_37464063_37491384 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 321 | 288 | 80 | 50 | 109 | 8 | 39 | 79 | MFNG_chr22_37464063_37491384 | MFNG | MQCRL others(316): Show |
chr22 | 37464063 | 37491384 |
| a0002 | 0/0 | 321 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | MFNG_chr22_37464063_37491384 | MFNG | MQCRL others(316): Show |
chr22 | 37464063 | 37491384 |
| a0003 | 0/0 | 321 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | MFNG_chr22_37464063_37491384 | MFNG | MQCRL others(316): Show |
chr22 | 37464063 | 37491384 |
| a0004 | 0/0 | 321 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | MFNG_chr22_37464063_37491384 | MFNG | MQCRL others(316): Show |
chr22 | 37464063 | 37491384 |
| a0005 | 0/0 | 321 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | MFNG_chr22_37464063_37491384 | MFNG | MQCRL others(316): Show |
chr22 | 37464063 | 37491384 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 963 | 283 | 76 | 50 | 108 | 8 | 39 | MFNG_chr22_37464063_37491384 | MFNG | ATGCA others(958): Show |
chr22 | 37464063 | 37491384 | ||
| a0001c0002 | 0/0 | 963 | 3 | 3 | 0 | 0 | 0 | 0 | MFNG_chr22_37464063_37491384 | MFNG | ATGCA others(958): Show |
chr22 | 37464063 | 37491384 | ||
| a0001c0007 | 0/0 | 963 | 1 | 0 | 0 | 1 | 0 | 0 | MFNG_chr22_37464063_37491384 | MFNG | ATGCA others(958): Show |
chr22 | 37464063 | 37491384 | ||
| a0001c0008 | 0/0 | 963 | 1 | 1 | 0 | 0 | 0 | 0 | MFNG_chr22_37464063_37491384 | MFNG | ATGCA others(958): Show |
chr22 | 37464063 | 37491384 | ||
| a0002c0003 | 0/0 | 963 | 1 | 1 | 0 | 0 | 0 | 0 | MFNG_chr22_37464063_37491384 | MFNG | ATGCA others(958): Show |
chr22 | 37464063 | 37491384 | ||
| a0003c0006 | 0/0 | 963 | 1 | 0 | 0 | 0 | 0 | 1 | MFNG_chr22_37464063_37491384 | MFNG | ATGCA others(958): Show |
chr22 | 37464063 | 37491384 | ||
| a0004c0005 | 0/0 | 963 | 1 | 0 | 0 | 1 | 0 | 0 | MFNG_chr22_37464063_37491384 | MFNG | ATGCA others(958): Show |
chr22 | 37464063 | 37491384 | ||
| a0005c0004 | 0/0 | 963 | 1 | 1 | 0 | 0 | 0 | 0 | MFNG_chr22_37464063_37491384 | MFNG | ATGCA others(958): Show |
chr22 | 37464063 | 37491384 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 1/1 | 2073 | 282 | 76 | 50 | 107 | 8 | 39 | MFNG_chr22_37464063_37491384 | MFNG | AGCAG others(2068): Show |
chr22 | 37464063 | 37491384 |
| a0001c0001t0002 | 0/0 | 1408 | 1 | 0 | 0 | 1 | 0 | 0 | MFNG_chr22_37464063_37491384 | MFNG | AGCAG others(1403): Show |
chr22 | 37464063 | 37491384 |
| a0001c0002t0001 | 0/0 | 2073 | 3 | 3 | 0 | 0 | 0 | 0 | MFNG_chr22_37464063_37491384 | MFNG | AGCAG others(2068): Show |
chr22 | 37464063 | 37491384 |
| a0001c0007t0001 | 0/0 | 2073 | 1 | 0 | 0 | 1 | 0 | 0 | MFNG_chr22_37464063_37491384 | MFNG | AGCAG others(2068): Show |
chr22 | 37464063 | 37491384 |
| a0001c0008t0001 | 0/0 | 2073 | 1 | 1 | 0 | 0 | 0 | 0 | MFNG_chr22_37464063_37491384 | MFNG | AGCAG others(2068): Show |
chr22 | 37464063 | 37491384 |
| a0002c0003t0001 | 0/0 | 2073 | 1 | 1 | 0 | 0 | 0 | 0 | MFNG_chr22_37464063_37491384 | MFNG | AGCAG others(2068): Show |
chr22 | 37464063 | 37491384 |
| a0003c0006t0001 | 0/0 | 2073 | 1 | 0 | 0 | 0 | 0 | 1 | MFNG_chr22_37464063_37491384 | MFNG | AGCAG others(2068): Show |
chr22 | 37464063 | 37491384 |
| a0004c0005t0001 | 0/0 | 2073 | 1 | 0 | 0 | 1 | 0 | 0 | MFNG_chr22_37464063_37491384 | MFNG | AGCAG others(2068): Show |
chr22 | 37464063 | 37491384 |
| a0005c0004t0001 | 0/0 | 2073 | 1 | 1 | 0 | 0 | 0 | 0 | MFNG_chr22_37464063_37491384 | MFNG | AGCAG others(2068): Show |
chr22 | 37464063 | 37491384 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 1/0 | 52 | 5 | 11 | 19 | 5 | 11 | MFNG_chr22_37464063_37491384 | MFNG | chr22 | 37464063 | 37491384 |
| a0001c0001t0001g0002 | 0/0 | 18 | 0 | 1 | 14 | 1 | 2 | MFNG_chr22_37464063_37491384 | MFNG | chr22 | 37464063 | 37491384 |
| a0001c0001t0001g0003 | 0/0 | 10 | 0 | 0 | 4 | 0 | 6 | MFNG_chr22_37464063_37491384 | MFNG | chr22 | 37464063 | 37491384 |
| a0001c0001t0001g0004 | 0/0 | 9 | 0 | 1 | 5 | 0 | 3 | MFNG_chr22_37464063_37491384 | MFNG | chr22 | 37464063 | 37491384 |
| a0001c0001t0001g0005 | 0/0 | 7 | 0 | 0 | 7 | 0 | 0 | MFNG_chr22_37464063_37491384 | MFNG | chr22 | 37464063 | 37491384 |
| a0001c0001t0001g0006 | 0/0 | 6 | 6 | 0 | 0 | 0 | 0 | MFNG_chr22_37464063_37491384 | MFNG | chr22 | 37464063 | 37491384 |
| a0001c0001t0001g0007 | 0/0 | 5 | 2 | 0 | 2 | 0 | 1 | MFNG_chr22_37464063_37491384 | MFNG | chr22 | 37464063 | 37491384 |
| a0001c0001t0001g0008 | 0/0 | 5 | 4 | 0 | 0 | 1 | 0 | MFNG_chr22_37464063_37491384 | MFNG | chr22 | 37464063 | 37491384 |
| a0001c0001t0001g0009 | 0/0 | 4 | 0 | 2 | 0 | 0 | 2 | MFNG_chr22_37464063_37491384 | MFNG | chr22 | 37464063 | 37491384 |
| a0001c0001t0001g0010 | 0/0 | 4 | 1 | 3 | 0 | 0 | 0 | MFNG_chr22_37464063_37491384 | MFNG | chr22 | 37464063 | 37491384 |
| a0001c0001t0001g0011 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | MFNG_chr22_37464063_37491384 | MFNG | chr22 | 37464063 | 37491384 |
| a0001c0001t0001g0012 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | MFNG_chr22_37464063_37491384 | MFNG | chr22 | 37464063 | 37491384 |
| a0001c0001t0001g0013 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | MFNG_chr22_37464063_37491384 | MFNG | chr22 | 37464063 | 37491384 |
| a0001c0001t0001g0014 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | MFNG_chr22_37464063_37491384 | MFNG | chr22 | 37464063 | 37491384 |
| a0001c0001t0001g0015 | 0/0 | 3 | 2 | 1 | 0 | 0 | 0 | MFNG_chr22_37464063_37491384 | MFNG | chr22 | 37464063 | 37491384 |
| a0001c0001t0001g0016 | 0/0 | 3 | 2 | 1 | 0 | 0 | 0 | MFNG_chr22_37464063_37491384 | MFNG | chr22 | 37464063 | 37491384 |
| a0001c0001t0001g0017 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | MFNG_chr22_37464063_37491384 | MFNG | chr22 | 37464063 | 37491384 |
| a0001c0001t0001g0018 | 0/0 | 3 | 0 | 1 | 2 | 0 | 0 | MFNG_chr22_37464063_37491384 | MFNG | chr22 | 37464063 | 37491384 |
| a0001c0001t0001g0019 | 0/0 | 2 | 1 | 0 | 1 | 0 | 0 | MFNG_chr22_37464063_37491384 | MFNG | chr22 | 37464063 | 37491384 |
| a0001c0001t0001g0020 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MFNG_chr22_37464063_37491384 | MFNG | chr22 | 37464063 | 37491384 |
| a0001c0001t0001g0021 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | MFNG_chr22_37464063_37491384 | MFNG | chr22 | 37464063 | 37491384 |
| a0001c0001t0001g0022 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MFNG_chr22_37464063_37491384 | MFNG | chr22 | 37464063 | 37491384 |
| a0001c0001t0001g0023 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MFNG_chr22_37464063_37491384 | MFNG | chr22 | 37464063 | 37491384 |
| a0001c0001t0001g0024 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | MFNG_chr22_37464063_37491384 | MFNG | chr22 | 37464063 | 37491384 |
| a0001c0001t0001g0026 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | MFNG_chr22_37464063_37491384 | MFNG | chr22 | 37464063 | 37491384 |
| a0001c0001t0001g0027 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | MFNG_chr22_37464063_37491384 | MFNG | chr22 | 37464063 | 37491384 |
| a0001c0001t0001g0028 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | MFNG_chr22_37464063_37491384 | MFNG | chr22 | 37464063 | 37491384 |
| a0001c0001t0001g0029 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | MFNG_chr22_37464063_37491384 | MFNG | chr22 | 37464063 | 37491384 |
| a0001c0001t0001g0030 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MFNG_chr22_37464063_37491384 | MFNG | chr22 | 37464063 | 37491384 |
| a0001c0001t0001g0031 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MFNG_chr22_37464063_37491384 | MFNG | chr22 | 37464063 | 37491384 |
| a0001c0001t0001g0032 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MFNG_chr22_37464063_37491384 | MFNG | chr22 | 37464063 | 37491384 |
| a0001c0001t0001g0033 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MFNG_chr22_37464063_37491384 | MFNG | chr22 | 37464063 | 37491384 |
| a0001c0001t0001g0034 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MFNG_chr22_37464063_37491384 | MFNG | chr22 | 37464063 | 37491384 |
| a0001c0001t0001g0035 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | MFNG_chr22_37464063_37491384 | MFNG | chr22 | 37464063 | 37491384 |
| a0001c0001t0001g0036 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | MFNG_chr22_37464063_37491384 | MFNG | chr22 | 37464063 | 37491384 |
| a0001c0001t0001g0037 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | MFNG_chr22_37464063_37491384 | MFNG | chr22 | 37464063 | 37491384 |
| a0001c0001t0001g0038 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MFNG_chr22_37464063_37491384 | MFNG | chr22 | 37464063 | 37491384 |
| a0001c0001t0001g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFNG_chr22_37464063_37491384 | MFNG | chr22 | 37464063 | 37491384 |
| a0001c0001t0001g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFNG_chr22_37464063_37491384 | MFNG | chr22 | 37464063 | 37491384 |
| a0001c0001t0001g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFNG_chr22_37464063_37491384 | MFNG | chr22 | 37464063 | 37491384 |
| a0001c0001t0001g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFNG_chr22_37464063_37491384 | MFNG | chr22 | 37464063 | 37491384 |
| a0001c0001t0001g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFNG_chr22_37464063_37491384 | MFNG | chr22 | 37464063 | 37491384 |
| a0001c0001t0001g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFNG_chr22_37464063_37491384 | MFNG | chr22 | 37464063 | 37491384 |
| a0001c0001t0001g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFNG_chr22_37464063_37491384 | MFNG | chr22 | 37464063 | 37491384 |
| a0001c0001t0001g0049 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MFNG_chr22_37464063_37491384 | MFNG | chr22 | 37464063 | 37491384 |
| a0001c0001t0001g0050 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MFNG_chr22_37464063_37491384 | MFNG | chr22 | 37464063 | 37491384 |
| a0001c0001t0001g0051 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MFNG_chr22_37464063_37491384 | MFNG | chr22 | 37464063 | 37491384 |
| a0001c0001t0001g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFNG_chr22_37464063_37491384 | MFNG | chr22 | 37464063 | 37491384 |
| a0001c0001t0001g0053 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MFNG_chr22_37464063_37491384 | MFNG | chr22 | 37464063 | 37491384 |
| a0001c0001t0001g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFNG_chr22_37464063_37491384 | MFNG | chr22 | 37464063 | 37491384 |
| a0001c0001t0001g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFNG_chr22_37464063_37491384 | MFNG | chr22 | 37464063 | 37491384 |
| a0001c0001t0001g0056 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MFNG_chr22_37464063_37491384 | MFNG | chr22 | 37464063 | 37491384 |
| a0001c0001t0001g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFNG_chr22_37464063_37491384 | MFNG | chr22 | 37464063 | 37491384 |
| a0001c0001t0001g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFNG_chr22_37464063_37491384 | MFNG | chr22 | 37464063 | 37491384 |
| a0001c0001t0001g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFNG_chr22_37464063_37491384 | MFNG | chr22 | 37464063 | 37491384 |
| a0001c0001t0001g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFNG_chr22_37464063_37491384 | MFNG | chr22 | 37464063 | 37491384 |
| a0001c0001t0001g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFNG_chr22_37464063_37491384 | MFNG | chr22 | 37464063 | 37491384 |
| a0001c0001t0001g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MFNG_chr22_37464063_37491384 | MFNG | chr22 | 37464063 | 37491384 |
| a0001c0001t0001g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFNG_chr22_37464063_37491384 | MFNG | chr22 | 37464063 | 37491384 |
| a0001c0001t0001g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFNG_chr22_37464063_37491384 | MFNG | chr22 | 37464063 | 37491384 |
| a0001c0001t0001g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFNG_chr22_37464063_37491384 | MFNG | chr22 | 37464063 | 37491384 |
| a0001c0001t0001g0067 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MFNG_chr22_37464063_37491384 | MFNG | chr22 | 37464063 | 37491384 |
| a0001c0001t0001g0069 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MFNG_chr22_37464063_37491384 | MFNG | chr22 | 37464063 | 37491384 |
| a0001c0001t0001g0070 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MFNG_chr22_37464063_37491384 | MFNG | chr22 | 37464063 | 37491384 |
| a0001c0001t0001g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFNG_chr22_37464063_37491384 | MFNG | chr22 | 37464063 | 37491384 |
| a0001c0001t0001g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFNG_chr22_37464063_37491384 | MFNG | chr22 | 37464063 | 37491384 |
| a0001c0001t0001g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MFNG_chr22_37464063_37491384 | MFNG | chr22 | 37464063 | 37491384 |
| a0001c0001t0001g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFNG_chr22_37464063_37491384 | MFNG | chr22 | 37464063 | 37491384 |
| a0001c0001t0001g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFNG_chr22_37464063_37491384 | MFNG | chr22 | 37464063 | 37491384 |
| a0001c0001t0001g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFNG_chr22_37464063_37491384 | MFNG | chr22 | 37464063 | 37491384 |
| a0001c0001t0001g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFNG_chr22_37464063_37491384 | MFNG | chr22 | 37464063 | 37491384 |
| a0001c0001t0001g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFNG_chr22_37464063_37491384 | MFNG | chr22 | 37464063 | 37491384 |
| a0001c0001t0001g0081 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MFNG_chr22_37464063_37491384 | MFNG | chr22 | 37464063 | 37491384 |
| a0001c0001t0001g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFNG_chr22_37464063_37491384 | MFNG | chr22 | 37464063 | 37491384 |
| a0001c0001t0001g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFNG_chr22_37464063_37491384 | MFNG | chr22 | 37464063 | 37491384 |
| a0001c0001t0001g0084 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MFNG_chr22_37464063_37491384 | MFNG | chr22 | 37464063 | 37491384 |
| a0001c0001t0001g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFNG_chr22_37464063_37491384 | MFNG | chr22 | 37464063 | 37491384 |
| a0001c0001t0001g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFNG_chr22_37464063_37491384 | MFNG | chr22 | 37464063 | 37491384 |
| a0001c0001t0001g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFNG_chr22_37464063_37491384 | MFNG | chr22 | 37464063 | 37491384 |
| a0001c0001t0001g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFNG_chr22_37464063_37491384 | MFNG | chr22 | 37464063 | 37491384 |
| a0001c0001t0001g0089 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MFNG_chr22_37464063_37491384 | MFNG | chr22 | 37464063 | 37491384 |
| a0001c0001t0001g0090 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MFNG_chr22_37464063_37491384 | MFNG | chr22 | 37464063 | 37491384 |
| a0001c0001t0001g0091 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MFNG_chr22_37464063_37491384 | MFNG | chr22 | 37464063 | 37491384 |
| a0001c0001t0001g0092 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MFNG_chr22_37464063_37491384 | MFNG | chr22 | 37464063 | 37491384 |
| a0001c0001t0001g0093 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MFNG_chr22_37464063_37491384 | MFNG | chr22 | 37464063 | 37491384 |
| a0001c0001t0001g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFNG_chr22_37464063_37491384 | MFNG | chr22 | 37464063 | 37491384 |
| a0001c0001t0001g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFNG_chr22_37464063_37491384 | MFNG | chr22 | 37464063 | 37491384 |
| a0001c0001t0001g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFNG_chr22_37464063_37491384 | MFNG | chr22 | 37464063 | 37491384 |
| a0001c0001t0001g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFNG_chr22_37464063_37491384 | MFNG | chr22 | 37464063 | 37491384 |
| a0001c0001t0001g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFNG_chr22_37464063_37491384 | MFNG | chr22 | 37464063 | 37491384 |
| a0001c0001t0001g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFNG_chr22_37464063_37491384 | MFNG | chr22 | 37464063 | 37491384 |
| a0001c0001t0001g0100 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MFNG_chr22_37464063_37491384 | MFNG | chr22 | 37464063 | 37491384 |
| a0001c0001t0001g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MFNG_chr22_37464063_37491384 | MFNG | chr22 | 37464063 | 37491384 |
| a0001c0001t0001g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFNG_chr22_37464063_37491384 | MFNG | chr22 | 37464063 | 37491384 |
| a0001c0001t0001g0103 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MFNG_chr22_37464063_37491384 | MFNG | chr22 | 37464063 | 37491384 |
| a0001c0001t0001g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFNG_chr22_37464063_37491384 | MFNG | chr22 | 37464063 | 37491384 |
| a0001c0001t0001g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFNG_chr22_37464063_37491384 | MFNG | chr22 | 37464063 | 37491384 |
| a0001c0001t0001g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFNG_chr22_37464063_37491384 | MFNG | chr22 | 37464063 | 37491384 |
| a0001c0001t0001g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFNG_chr22_37464063_37491384 | MFNG | chr22 | 37464063 | 37491384 |
| a0001c0001t0001g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFNG_chr22_37464063_37491384 | MFNG | chr22 | 37464063 | 37491384 |
| a0001c0001t0001g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFNG_chr22_37464063_37491384 | MFNG | chr22 | 37464063 | 37491384 |
| a0001c0001t0001g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFNG_chr22_37464063_37491384 | MFNG | chr22 | 37464063 | 37491384 |
| a0001c0001t0001g0111 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MFNG_chr22_37464063_37491384 | MFNG | chr22 | 37464063 | 37491384 |
| a0001c0001t0001g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFNG_chr22_37464063_37491384 | MFNG | chr22 | 37464063 | 37491384 |
| a0001c0001t0001g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFNG_chr22_37464063_37491384 | MFNG | chr22 | 37464063 | 37491384 |
| a0001c0001t0001g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFNG_chr22_37464063_37491384 | MFNG | chr22 | 37464063 | 37491384 |
| a0001c0001t0001g0115 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MFNG_chr22_37464063_37491384 | MFNG | chr22 | 37464063 | 37491384 |
| a0001c0001t0001g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFNG_chr22_37464063_37491384 | MFNG | chr22 | 37464063 | 37491384 |
| a0001c0001t0001g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFNG_chr22_37464063_37491384 | MFNG | chr22 | 37464063 | 37491384 |
| a0001c0001t0001g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFNG_chr22_37464063_37491384 | MFNG | chr22 | 37464063 | 37491384 |
| a0001c0001t0001g0119 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MFNG_chr22_37464063_37491384 | MFNG | chr22 | 37464063 | 37491384 |
| a0001c0001t0001g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFNG_chr22_37464063_37491384 | MFNG | chr22 | 37464063 | 37491384 |
| a0001c0001t0001g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFNG_chr22_37464063_37491384 | MFNG | chr22 | 37464063 | 37491384 |
| a0001c0001t0001g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFNG_chr22_37464063_37491384 | MFNG | chr22 | 37464063 | 37491384 |
| a0001c0001t0001g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFNG_chr22_37464063_37491384 | MFNG | chr22 | 37464063 | 37491384 |
| a0001c0001t0001g0124 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MFNG_chr22_37464063_37491384 | MFNG | chr22 | 37464063 | 37491384 |
| a0001c0001t0001g0125 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MFNG_chr22_37464063_37491384 | MFNG | chr22 | 37464063 | 37491384 |
| a0001c0001t0001g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFNG_chr22_37464063_37491384 | MFNG | chr22 | 37464063 | 37491384 |
| a0001c0001t0001g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFNG_chr22_37464063_37491384 | MFNG | chr22 | 37464063 | 37491384 |
| a0001c0001t0001g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFNG_chr22_37464063_37491384 | MFNG | chr22 | 37464063 | 37491384 |
| a0001c0001t0001g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFNG_chr22_37464063_37491384 | MFNG | chr22 | 37464063 | 37491384 |
| a0001c0001t0001g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFNG_chr22_37464063_37491384 | MFNG | chr22 | 37464063 | 37491384 |
| a0001c0001t0001g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFNG_chr22_37464063_37491384 | MFNG | chr22 | 37464063 | 37491384 |
| a0001c0001t0001g0132 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MFNG_chr22_37464063_37491384 | MFNG | chr22 | 37464063 | 37491384 |
| a0001c0001t0001g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFNG_chr22_37464063_37491384 | MFNG | chr22 | 37464063 | 37491384 |
| a0001c0001t0001g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFNG_chr22_37464063_37491384 | MFNG | chr22 | 37464063 | 37491384 |
| a0001c0001t0001g0135 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MFNG_chr22_37464063_37491384 | MFNG | chr22 | 37464063 | 37491384 |
| a0001c0001t0001g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFNG_chr22_37464063_37491384 | MFNG | chr22 | 37464063 | 37491384 |
| a0001c0001t0001g0137 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | MFNG_chr22_37464063_37491384 | MFNG | chr22 | 37464063 | 37491384 |
| a0001c0001t0001g0138 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MFNG_chr22_37464063_37491384 | MFNG | chr22 | 37464063 | 37491384 |
| a0001c0001t0001g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFNG_chr22_37464063_37491384 | MFNG | chr22 | 37464063 | 37491384 |
| a0001c0001t0001g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFNG_chr22_37464063_37491384 | MFNG | chr22 | 37464063 | 37491384 |
| a0001c0001t0001g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFNG_chr22_37464063_37491384 | MFNG | chr22 | 37464063 | 37491384 |
| a0001c0001t0001g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFNG_chr22_37464063_37491384 | MFNG | chr22 | 37464063 | 37491384 |
| a0001c0001t0001g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFNG_chr22_37464063_37491384 | MFNG | chr22 | 37464063 | 37491384 |
| a0001c0001t0002g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFNG_chr22_37464063_37491384 | MFNG | chr22 | 37464063 | 37491384 |
| a0001c0002t0001g0025 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MFNG_chr22_37464063_37491384 | MFNG | chr22 | 37464063 | 37491384 |
| a0001c0002t0001g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFNG_chr22_37464063_37491384 | MFNG | chr22 | 37464063 | 37491384 |
| a0001c0007t0001g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFNG_chr22_37464063_37491384 | MFNG | chr22 | 37464063 | 37491384 |
| a0001c0008t0001g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFNG_chr22_37464063_37491384 | MFNG | chr22 | 37464063 | 37491384 |
| a0002c0003t0001g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFNG_chr22_37464063_37491384 | MFNG | chr22 | 37464063 | 37491384 |
| a0003c0006t0001g0058 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MFNG_chr22_37464063_37491384 | MFNG | chr22 | 37464063 | 37491384 |
| a0004c0005t0001g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFNG_chr22_37464063_37491384 | MFNG | chr22 | 37464063 | 37491384 |
| a0005c0004t0001g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFNG_chr22_37464063_37491384 | MFNG | chr22 | 37464063 | 37491384 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00140 | hp1 | a0001 | c0001 | t0001 | g0001 | EUR | GBR | MFNG_chr22_37464063_37491384 | MFNG | chr22 | 37464063 | 37491384 |
| HG00140 | hp2 | a0001 | c0001 | t0001 | g0001 | EUR | GBR | MFNG_chr22_37464063_37491384 | MFNG | chr22 | 37464063 | 37491384 |
| HG00323 | hp1 | a0001 | c0001 | t0001 | g0001 | EUR | FIN | MFNG_chr22_37464063_37491384 | MFNG | chr22 | 37464063 | 37491384 |
| HG00323 | hp2 | a0001 | c0001 | t0001 | g0002 | EUR | FIN | MFNG_chr22_37464063_37491384 | MFNG | chr22 | 37464063 | 37491384 |
| HG00408 | hp1 | a0001 | c0001 | t0001 | g0079 | EAS | CHS | MFNG_chr22_37464063_37491384 | MFNG | chr22 | 37464063 | 37491384 |
| HG00408 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | MFNG_chr22_37464063_37491384 | MFNG | chr22 | 37464063 | 37491384 |
| HG00438 | hp1 | a0001 | c0001 | t0001 | g0037 | EAS | CHS | MFNG_chr22_37464063_37491384 | MFNG | chr22 | 37464063 | 37491384 |
| HG00438 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | MFNG_chr22_37464063_37491384 | MFNG | chr22 | 37464063 | 37491384 |
| HG00544 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | CHS | MFNG_chr22_37464063_37491384 | MFNG | chr22 | 37464063 | 37491384 |
| HG00544 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | MFNG_chr22_37464063_37491384 | MFNG | chr22 | 37464063 | 37491384 |
| HG00558 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | CHS | MFNG_chr22_37464063_37491384 | MFNG | chr22 | 37464063 | 37491384 |
| HG00558 | hp2 | a0001 | c0001 | t0001 | g0130 | EAS | CHS | MFNG_chr22_37464063_37491384 | MFNG | chr22 | 37464063 | 37491384 |
| HG00597 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | MFNG_chr22_37464063_37491384 | MFNG | chr22 | 37464063 | 37491384 |
| HG00597 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | CHS | MFNG_chr22_37464063_37491384 | MFNG | chr22 | 37464063 | 37491384 |
| HG00609 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | CHS | MFNG_chr22_37464063_37491384 | MFNG | chr22 | 37464063 | 37491384 |
| HG00609 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | MFNG_chr22_37464063_37491384 | MFNG | chr22 | 37464063 | 37491384 |
| HG00621 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | CHS | MFNG_chr22_37464063_37491384 | MFNG | chr22 | 37464063 | 37491384 |
| HG00621 | hp2 | a0001 | c0001 | t0001 | g0034 | EAS | CHS | MFNG_chr22_37464063_37491384 | MFNG | chr22 | 37464063 | 37491384 |
| HG00639 | hp1 | a0001 | c0001 | t0001 | g0027 | AMR | PUR | MFNG_chr22_37464063_37491384 | MFNG | chr22 | 37464063 | 37491384 |
| HG00639 | hp2 | a0001 | c0001 | t0001 | g0015 | AMR | PUR | MFNG_chr22_37464063_37491384 | MFNG | chr22 | 37464063 | 37491384 |
| HG00642 | hp1 | a0001 | c0001 | t0001 | g0053 | AMR | PUR | MFNG_chr22_37464063_37491384 | MFNG | chr22 | 37464063 | 37491384 |
| HG00642 | hp2 | a0001 | c0001 | t0001 | g0010 | AMR | PUR | MFNG_chr22_37464063_37491384 | MFNG | chr22 | 37464063 | 37491384 |
| HG00735 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | MFNG_chr22_37464063_37491384 | MFNG | chr22 | 37464063 | 37491384 |
| HG00735 | hp2 | a0001 | c0001 | t0001 | g0029 | AMR | PUR | MFNG_chr22_37464063_37491384 | MFNG | chr22 | 37464063 | 37491384 |
| HG00738 | hp1 | a0001 | c0001 | t0001 | g0135 | AMR | PUR | MFNG_chr22_37464063_37491384 | MFNG | chr22 | 37464063 | 37491384 |
| HG00738 | hp2 | a0001 | c0001 | t0001 | g0017 | AMR | PUR | MFNG_chr22_37464063_37491384 | MFNG | chr22 | 37464063 | 37491384 |
| HG00741 | hp1 | a0001 | c0001 | t0001 | g0029 | AMR | PUR | MFNG_chr22_37464063_37491384 | MFNG | chr22 | 37464063 | 37491384 |
| HG00741 | hp2 | a0001 | c0001 | t0001 | g0091 | AMR | PUR | MFNG_chr22_37464063_37491384 | MFNG | chr22 | 37464063 | 37491384 |
| HG01069 | hp1 | a0001 | c0001 | t0001 | g0090 | AMR | PUR | MFNG_chr22_37464063_37491384 | MFNG | chr22 | 37464063 | 37491384 |
| HG01069 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | MFNG_chr22_37464063_37491384 | MFNG | chr22 | 37464063 | 37491384 |
| HG01074 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | MFNG_chr22_37464063_37491384 | MFNG | chr22 | 37464063 | 37491384 |
| HG01074 | hp2 | a0001 | c0001 | t0001 | g0017 | AMR | PUR | MFNG_chr22_37464063_37491384 | MFNG | chr22 | 37464063 | 37491384 |
| HG01081 | hp1 | a0001 | c0001 | t0001 | g0056 | AMR | PUR | MFNG_chr22_37464063_37491384 | MFNG | chr22 | 37464063 | 37491384 |
| HG01081 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | MFNG_chr22_37464063_37491384 | MFNG | chr22 | 37464063 | 37491384 |
| HG01099 | hp1 | a0001 | c0001 | t0001 | g0036 | AMR | PUR | MFNG_chr22_37464063_37491384 | MFNG | chr22 | 37464063 | 37491384 |
| HG01099 | hp2 | a0001 | c0001 | t0001 | g0028 | AMR | PUR | MFNG_chr22_37464063_37491384 | MFNG | chr22 | 37464063 | 37491384 |
| HG01106 | hp1 | a0001 | c0001 | t0001 | g0017 | AMR | PUR | MFNG_chr22_37464063_37491384 | MFNG | chr22 | 37464063 | 37491384 |
| HG01106 | hp2 | a0001 | c0001 | t0001 | g0004 | AMR | PUR | MFNG_chr22_37464063_37491384 | MFNG | chr22 | 37464063 | 37491384 |
| HG01109 | hp1 | a0001 | c0001 | t0001 | g0125 | AMR | PUR | MFNG_chr22_37464063_37491384 | MFNG | chr22 | 37464063 | 37491384 |
| HG01109 | hp2 | a0001 | c0001 | t0001 | g0100 | AMR | PUR | MFNG_chr22_37464063_37491384 | MFNG | chr22 | 37464063 | 37491384 |
| HG01167 | hp1 | a0001 | c0001 | t0001 | g0010 | AMR | PUR | MFNG_chr22_37464063_37491384 | MFNG | chr22 | 37464063 | 37491384 |
| HG01167 | hp2 | a0001 | c0001 | t0001 | g0089 | AMR | PUR | MFNG_chr22_37464063_37491384 | MFNG | chr22 | 37464063 | 37491384 |
| HG01169 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | MFNG_chr22_37464063_37491384 | MFNG | chr22 | 37464063 | 37491384 |
| HG01169 | hp2 | a0001 | c0001 | t0001 | g0010 | AMR | PUR | MFNG_chr22_37464063_37491384 | MFNG | chr22 | 37464063 | 37491384 |
| HG01175 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | MFNG_chr22_37464063_37491384 | MFNG | chr22 | 37464063 | 37491384 |
| HG01175 | hp2 | a0001 | c0001 | t0001 | g0024 | AMR | PUR | MFNG_chr22_37464063_37491384 | MFNG | chr22 | 37464063 | 37491384 |
| HG01192 | hp1 | a0001 | c0001 | t0001 | g0115 | AMR | PUR | MFNG_chr22_37464063_37491384 | MFNG | chr22 | 37464063 | 37491384 |
| HG01192 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | MFNG_chr22_37464063_37491384 | MFNG | chr22 | 37464063 | 37491384 |
| HG01243 | hp1 | a0001 | c0001 | t0001 | g0016 | AMR | PUR | MFNG_chr22_37464063_37491384 | MFNG | chr22 | 37464063 | 37491384 |
| HG01243 | hp2 | a0001 | c0001 | t0001 | g0119 | AMR | PUR | MFNG_chr22_37464063_37491384 | MFNG | chr22 | 37464063 | 37491384 |
| HG01256 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | CLM | MFNG_chr22_37464063_37491384 | MFNG | chr22 | 37464063 | 37491384 |
| HG01256 | hp2 | a0001 | c0001 | t0001 | g0009 | AMR | CLM | MFNG_chr22_37464063_37491384 | MFNG | chr22 | 37464063 | 37491384 |
| HG01257 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | MFNG_chr22_37464063_37491384 | MFNG | chr22 | 37464063 | 37491384 |
| HG01257 | hp2 | a0001 | c0001 | t0001 | g0035 | AMR | CLM | MFNG_chr22_37464063_37491384 | MFNG | chr22 | 37464063 | 37491384 |
| HG01258 | hp1 | a0001 | c0001 | t0001 | g0009 | AMR | CLM | MFNG_chr22_37464063_37491384 | MFNG | chr22 | 37464063 | 37491384 |
| HG01258 | hp2 | a0001 | c0001 | t0001 | g0035 | AMR | CLM | MFNG_chr22_37464063_37491384 | MFNG | chr22 | 37464063 | 37491384 |
| HG01346 | hp1 | a0001 | c0001 | t0001 | g0063 | AMR | CLM | MFNG_chr22_37464063_37491384 | MFNG | chr22 | 37464063 | 37491384 |
| HG01346 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | MFNG_chr22_37464063_37491384 | MFNG | chr22 | 37464063 | 37491384 |
| HG01361 | hp1 | a0001 | c0001 | t0001 | g0069 | AMR | CLM | MFNG_chr22_37464063_37491384 | MFNG | chr22 | 37464063 | 37491384 |
| HG01361 | hp2 | a0001 | c0001 | t0001 | g0018 | AMR | CLM | MFNG_chr22_37464063_37491384 | MFNG | chr22 | 37464063 | 37491384 |
| HG01433 | hp1 | a0001 | c0001 | t0001 | g0101 | AMR | CLM | MFNG_chr22_37464063_37491384 | MFNG | chr22 | 37464063 | 37491384 |
| HG01433 | hp2 | a0001 | c0001 | t0001 | g0132 | AMR | CLM | MFNG_chr22_37464063_37491384 | MFNG | chr22 | 37464063 | 37491384 |
| HG01496 | hp1 | a0001 | c0001 | t0001 | g0021 | AMR | CLM | MFNG_chr22_37464063_37491384 | MFNG | chr22 | 37464063 | 37491384 |
| HG01496 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | MFNG_chr22_37464063_37491384 | MFNG | chr22 | 37464063 | 37491384 |
| HG01515 | hp1 | a0001 | c0001 | t0001 | g0001 | EUR | IBS | MFNG_chr22_37464063_37491384 | MFNG | chr22 | 37464063 | 37491384 |
| HG01515 | hp2 | a0001 | c0001 | t0001 | g0111 | EUR | IBS | MFNG_chr22_37464063_37491384 | MFNG | chr22 | 37464063 | 37491384 |
| HG01884 | hp1 | a0001 | c0001 | t0001 | g0020 | AFR | ACB | MFNG_chr22_37464063_37491384 | MFNG | chr22 | 37464063 | 37491384 |
| HG01884 | hp2 | a0001 | c0001 | t0001 | g0016 | AFR | ACB | MFNG_chr22_37464063_37491384 | MFNG | chr22 | 37464063 | 37491384 |
| HG01928 | hp1 | a0001 | c0001 | t0001 | g0070 | AMR | PEL | MFNG_chr22_37464063_37491384 | MFNG | chr22 | 37464063 | 37491384 |
| HG01928 | hp2 | a0001 | c0001 | t0001 | g0037 | AMR | PEL | MFNG_chr22_37464063_37491384 | MFNG | chr22 | 37464063 | 37491384 |
| HG01981 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | MFNG_chr22_37464063_37491384 | MFNG | chr22 | 37464063 | 37491384 |
| HG01981 | hp2 | a0001 | c0001 | t0001 | g0073 | AMR | PEL | MFNG_chr22_37464063_37491384 | MFNG | chr22 | 37464063 | 37491384 |
| HG02055 | hp1 | a0001 | c0001 | t0001 | g0121 | AFR | ACB | MFNG_chr22_37464063_37491384 | MFNG | chr22 | 37464063 | 37491384 |
| HG02055 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | ACB | MFNG_chr22_37464063_37491384 | MFNG | chr22 | 37464063 | 37491384 |
| HG02056 | hp1 | a0001 | c0001 | t0001 | g0014 | EAS | KHV | MFNG_chr22_37464063_37491384 | MFNG | chr22 | 37464063 | 37491384 |
| HG02056 | hp2 | a0001 | c0001 | t0001 | g0019 | EAS | KHV | MFNG_chr22_37464063_37491384 | MFNG | chr22 | 37464063 | 37491384 |
| HG02074 | hp1 | a0001 | c0001 | t0001 | g0007 | EAS | KHV | MFNG_chr22_37464063_37491384 | MFNG | chr22 | 37464063 | 37491384 |
| HG02074 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | KHV | MFNG_chr22_37464063_37491384 | MFNG | chr22 | 37464063 | 37491384 |
| HG02080 | hp1 | a0001 | c0001 | t0001 | g0078 | EAS | KHV | MFNG_chr22_37464063_37491384 | MFNG | chr22 | 37464063 | 37491384 |
| HG02080 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | KHV | MFNG_chr22_37464063_37491384 | MFNG | chr22 | 37464063 | 37491384 |
| HG02083 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | KHV | MFNG_chr22_37464063_37491384 | MFNG | chr22 | 37464063 | 37491384 |
| HG02083 | hp2 | a0001 | c0001 | t0001 | g0102 | EAS | KHV | MFNG_chr22_37464063_37491384 | MFNG | chr22 | 37464063 | 37491384 |
| HG02132 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | KHV | MFNG_chr22_37464063_37491384 | MFNG | chr22 | 37464063 | 37491384 |
| HG02132 | hp2 | a0001 | c0001 | t0001 | g0109 | EAS | KHV | MFNG_chr22_37464063_37491384 | MFNG | chr22 | 37464063 | 37491384 |
| HG02145 | hp1 | a0001 | c0001 | t0001 | g0019 | AFR | ACB | MFNG_chr22_37464063_37491384 | MFNG | chr22 | 37464063 | 37491384 |
| HG02145 | hp2 | a0001 | c0001 | t0001 | g0028 | AFR | ACB | MFNG_chr22_37464063_37491384 | MFNG | chr22 | 37464063 | 37491384 |
| HG02155 | hp1 | a0001 | c0001 | t0001 | g0012 | EAS | CDX | MFNG_chr22_37464063_37491384 | MFNG | chr22 | 37464063 | 37491384 |
| HG02155 | hp2 | a0001 | c0001 | t0001 | g0042 | EAS | CDX | MFNG_chr22_37464063_37491384 | MFNG | chr22 | 37464063 | 37491384 |
| HG02165 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | CDX | MFNG_chr22_37464063_37491384 | MFNG | chr22 | 37464063 | 37491384 |
| HG02165 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CDX | MFNG_chr22_37464063_37491384 | MFNG | chr22 | 37464063 | 37491384 |
| HG02257 | hp1 | a0001 | c0001 | t0001 | g0094 | AFR | ACB | MFNG_chr22_37464063_37491384 | MFNG | chr22 | 37464063 | 37491384 |
| HG02257 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | ACB | MFNG_chr22_37464063_37491384 | MFNG | chr22 | 37464063 | 37491384 |
| HG02258 | hp1 | a0001 | c0001 | t0001 | g0030 | AFR | ACB | MFNG_chr22_37464063_37491384 | MFNG | chr22 | 37464063 | 37491384 |
| HG02258 | hp2 | a0001 | c0001 | t0001 | g0013 | AFR | ACB | MFNG_chr22_37464063_37491384 | MFNG | chr22 | 37464063 | 37491384 |
| HG02451 | hp1 | a0001 | c0001 | t0001 | g0027 | AFR | ACB | MFNG_chr22_37464063_37491384 | MFNG | chr22 | 37464063 | 37491384 |
| HG02451 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | ACB | MFNG_chr22_37464063_37491384 | MFNG | chr22 | 37464063 | 37491384 |
| HG02572 | hp1 | a0001 | c0001 | t0001 | g0040 | AFR | GWD | MFNG_chr22_37464063_37491384 | MFNG | chr22 | 37464063 | 37491384 |
| HG02572 | hp2 | a0001 | c0001 | t0001 | g0112 | AFR | GWD | MFNG_chr22_37464063_37491384 | MFNG | chr22 | 37464063 | 37491384 |
| HG02602 | hp1 | a0001 | c0001 | t0001 | g0004 | SAS | PJL | MFNG_chr22_37464063_37491384 | MFNG | chr22 | 37464063 | 37491384 |
| HG02602 | hp2 | a0001 | c0001 | t0001 | g0003 | SAS | PJL | MFNG_chr22_37464063_37491384 | MFNG | chr22 | 37464063 | 37491384 |
| HG02615 | hp1 | a0001 | c0001 | t0001 | g0065 | AFR | GWD | MFNG_chr22_37464063_37491384 | MFNG | chr22 | 37464063 | 37491384 |
| HG02615 | hp2 | a0001 | c0001 | t0001 | g0010 | AFR | GWD | MFNG_chr22_37464063_37491384 | MFNG | chr22 | 37464063 | 37491384 |
| HG02622 | hp1 | a0001 | c0008 | t0001 | g0144 | AFR | GWD | MFNG_chr22_37464063_37491384 | MFNG | chr22 | 37464063 | 37491384 |
| HG02622 | hp2 | a0001 | c0001 | t0001 | g0033 | AFR | GWD | MFNG_chr22_37464063_37491384 | MFNG | chr22 | 37464063 | 37491384 |
| HG02647 | hp1 | a0001 | c0001 | t0001 | g0118 | AFR | GWD | MFNG_chr22_37464063_37491384 | MFNG | chr22 | 37464063 | 37491384 |
| HG02647 | hp2 | a0001 | c0001 | t0001 | g0015 | AFR | GWD | MFNG_chr22_37464063_37491384 | MFNG | chr22 | 37464063 | 37491384 |
| HG02683 | hp1 | a0001 | c0001 | t0001 | g0024 | SAS | PJL | MFNG_chr22_37464063_37491384 | MFNG | chr22 | 37464063 | 37491384 |
| HG02683 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | MFNG_chr22_37464063_37491384 | MFNG | chr22 | 37464063 | 37491384 |
| HG02717 | hp1 | a0001 | c0001 | t0001 | g0011 | AFR | GWD | MFNG_chr22_37464063_37491384 | MFNG | chr22 | 37464063 | 37491384 |
| HG02717 | hp2 | a0001 | c0001 | t0001 | g0116 | AFR | GWD | MFNG_chr22_37464063_37491384 | MFNG | chr22 | 37464063 | 37491384 |
| HG02723 | hp1 | a0001 | c0001 | t0001 | g0087 | AFR | GWD | MFNG_chr22_37464063_37491384 | MFNG | chr22 | 37464063 | 37491384 |
| HG02723 | hp2 | a0001 | c0001 | t0001 | g0055 | AFR | GWD | MFNG_chr22_37464063_37491384 | MFNG | chr22 | 37464063 | 37491384 |
| HG02735 | hp1 | a0001 | c0001 | t0001 | g0026 | SAS | PJL | MFNG_chr22_37464063_37491384 | MFNG | chr22 | 37464063 | 37491384 |
| HG02735 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | MFNG_chr22_37464063_37491384 | MFNG | chr22 | 37464063 | 37491384 |
| HG02738 | hp1 | a0001 | c0001 | t0001 | g0007 | SAS | PJL | MFNG_chr22_37464063_37491384 | MFNG | chr22 | 37464063 | 37491384 |
| HG02738 | hp2 | a0001 | c0001 | t0001 | g0026 | SAS | PJL | MFNG_chr22_37464063_37491384 | MFNG | chr22 | 37464063 | 37491384 |
| HG02809 | hp1 | a0001 | c0001 | t0001 | g0064 | AFR | GWD | MFNG_chr22_37464063_37491384 | MFNG | chr22 | 37464063 | 37491384 |
| HG02809 | hp2 | a0001 | c0001 | t0001 | g0117 | AFR | GWD | MFNG_chr22_37464063_37491384 | MFNG | chr22 | 37464063 | 37491384 |
| HG02886 | hp1 | a0001 | c0001 | t0001 | g0128 | AFR | GWD | MFNG_chr22_37464063_37491384 | MFNG | chr22 | 37464063 | 37491384 |
| HG02886 | hp2 | a0001 | c0001 | t0001 | g0008 | AFR | GWD | MFNG_chr22_37464063_37491384 | MFNG | chr22 | 37464063 | 37491384 |
| HG02895 | hp1 | a0001 | c0001 | t0001 | g0007 | AFR | GWD | MFNG_chr22_37464063_37491384 | MFNG | chr22 | 37464063 | 37491384 |
| HG02895 | hp2 | a0001 | c0001 | t0001 | g0006 | AFR | GWD | MFNG_chr22_37464063_37491384 | MFNG | chr22 | 37464063 | 37491384 |
| HG02896 | hp1 | a0001 | c0001 | t0001 | g0072 | AFR | GWD | MFNG_chr22_37464063_37491384 | MFNG | chr22 | 37464063 | 37491384 |
| HG02896 | hp2 | a0001 | c0001 | t0001 | g0114 | AFR | GWD | MFNG_chr22_37464063_37491384 | MFNG | chr22 | 37464063 | 37491384 |
| HG02897 | hp1 | a0001 | c0001 | t0001 | g0071 | AFR | GWD | MFNG_chr22_37464063_37491384 | MFNG | chr22 | 37464063 | 37491384 |
| HG02897 | hp2 | a0001 | c0001 | t0001 | g0006 | AFR | GWD | MFNG_chr22_37464063_37491384 | MFNG | chr22 | 37464063 | 37491384 |
| HG02965 | hp1 | a0001 | c0001 | t0001 | g0006 | AFR | ESN | MFNG_chr22_37464063_37491384 | MFNG | chr22 | 37464063 | 37491384 |
| HG02965 | hp2 | a0001 | c0001 | t0001 | g0127 | AFR | ESN | MFNG_chr22_37464063_37491384 | MFNG | chr22 | 37464063 | 37491384 |
| HG02970 | hp1 | a0001 | c0001 | t0001 | g0016 | AFR | ESN | MFNG_chr22_37464063_37491384 | MFNG | chr22 | 37464063 | 37491384 |
| HG02970 | hp2 | a0001 | c0001 | t0001 | g0011 | AFR | ESN | MFNG_chr22_37464063_37491384 | MFNG | chr22 | 37464063 | 37491384 |
| HG02976 | hp1 | a0001 | c0001 | t0001 | g0011 | AFR | ESN | MFNG_chr22_37464063_37491384 | MFNG | chr22 | 37464063 | 37491384 |
| HG02976 | hp2 | a0001 | c0001 | t0001 | g0099 | AFR | ESN | MFNG_chr22_37464063_37491384 | MFNG | chr22 | 37464063 | 37491384 |
| HG03017 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | MFNG_chr22_37464063_37491384 | MFNG | chr22 | 37464063 | 37491384 |
| HG03017 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | MFNG_chr22_37464063_37491384 | MFNG | chr22 | 37464063 | 37491384 |
| HG03041 | hp1 | a0001 | c0001 | t0001 | g0062 | AFR | GWD | MFNG_chr22_37464063_37491384 | MFNG | chr22 | 37464063 | 37491384 |
| HG03041 | hp2 | a0001 | c0001 | t0001 | g0007 | AFR | GWD | MFNG_chr22_37464063_37491384 | MFNG | chr22 | 37464063 | 37491384 |
| HG03098 | hp1 | a0001 | c0001 | t0001 | g0095 | AFR | MSL | MFNG_chr22_37464063_37491384 | MFNG | chr22 | 37464063 | 37491384 |
| HG03098 | hp2 | a0001 | c0002 | t0001 | g0025 | AFR | MSL | MFNG_chr22_37464063_37491384 | MFNG | chr22 | 37464063 | 37491384 |
| HG03130 | hp1 | a0001 | c0001 | t0001 | g0006 | AFR | ESN | MFNG_chr22_37464063_37491384 | MFNG | chr22 | 37464063 | 37491384 |
| HG03130 | hp2 | a0001 | c0001 | t0001 | g0021 | AFR | ESN | MFNG_chr22_37464063_37491384 | MFNG | chr22 | 37464063 | 37491384 |
| HG03195 | hp1 | a0001 | c0001 | t0001 | g0108 | AFR | ESN | MFNG_chr22_37464063_37491384 | MFNG | chr22 | 37464063 | 37491384 |
| HG03195 | hp2 | a0001 | c0001 | t0001 | g0085 | AFR | ESN | MFNG_chr22_37464063_37491384 | MFNG | chr22 | 37464063 | 37491384 |
| HG03209 | hp1 | a0001 | c0001 | t0001 | g0011 | AFR | MSL | MFNG_chr22_37464063_37491384 | MFNG | chr22 | 37464063 | 37491384 |
| HG03209 | hp2 | a0001 | c0001 | t0001 | g0105 | AFR | MSL | MFNG_chr22_37464063_37491384 | MFNG | chr22 | 37464063 | 37491384 |
| HG03225 | hp1 | a0001 | c0001 | t0001 | g0020 | AFR | MSL | MFNG_chr22_37464063_37491384 | MFNG | chr22 | 37464063 | 37491384 |
| HG03225 | hp2 | a0001 | c0001 | t0001 | g0097 | AFR | MSL | MFNG_chr22_37464063_37491384 | MFNG | chr22 | 37464063 | 37491384 |
| HG03239 | hp1 | a0001 | c0001 | t0001 | g0003 | SAS | PJL | MFNG_chr22_37464063_37491384 | MFNG | chr22 | 37464063 | 37491384 |
| HG03239 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | MFNG_chr22_37464063_37491384 | MFNG | chr22 | 37464063 | 37491384 |
| HG03453 | hp1 | a0001 | c0001 | t0001 | g0033 | AFR | MSL | MFNG_chr22_37464063_37491384 | MFNG | chr22 | 37464063 | 37491384 |
| HG03453 | hp2 | a0001 | c0002 | t0001 | g0044 | AFR | MSL | MFNG_chr22_37464063_37491384 | MFNG | chr22 | 37464063 | 37491384 |
| HG03486 | hp1 | a0001 | c0001 | t0001 | g0006 | AFR | MSL | MFNG_chr22_37464063_37491384 | MFNG | chr22 | 37464063 | 37491384 |
| HG03486 | hp2 | a0001 | c0001 | t0001 | g0096 | AFR | MSL | MFNG_chr22_37464063_37491384 | MFNG | chr22 | 37464063 | 37491384 |
| HG03490 | hp1 | a0001 | c0001 | t0001 | g0093 | SAS | PJL | MFNG_chr22_37464063_37491384 | MFNG | chr22 | 37464063 | 37491384 |
| HG03490 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | MFNG_chr22_37464063_37491384 | MFNG | chr22 | 37464063 | 37491384 |
| HG03516 | hp1 | a0001 | c0002 | t0001 | g0025 | AFR | ESN | MFNG_chr22_37464063_37491384 | MFNG | chr22 | 37464063 | 37491384 |
| HG03516 | hp2 | a0001 | c0001 | t0001 | g0047 | AFR | ESN | MFNG_chr22_37464063_37491384 | MFNG | chr22 | 37464063 | 37491384 |
| HG03579 | hp1 | a0001 | c0001 | t0001 | g0015 | AFR | MSL | MFNG_chr22_37464063_37491384 | MFNG | chr22 | 37464063 | 37491384 |
| HG03579 | hp2 | a0001 | c0001 | t0001 | g0006 | AFR | MSL | MFNG_chr22_37464063_37491384 | MFNG | chr22 | 37464063 | 37491384 |
| HG03654 | hp1 | a0001 | c0001 | t0001 | g0103 | SAS | PJL | MFNG_chr22_37464063_37491384 | MFNG | chr22 | 37464063 | 37491384 |
| HG03654 | hp2 | a0001 | c0001 | t0001 | g0067 | SAS | PJL | MFNG_chr22_37464063_37491384 | MFNG | chr22 | 37464063 | 37491384 |
| HG03669 | hp1 | a0001 | c0001 | t0001 | g0002 | SAS | PJL | MFNG_chr22_37464063_37491384 | MFNG | chr22 | 37464063 | 37491384 |
| HG03669 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | MFNG_chr22_37464063_37491384 | MFNG | chr22 | 37464063 | 37491384 |
| HG03688 | hp1 | a0001 | c0001 | t0001 | g0049 | SAS | STU | MFNG_chr22_37464063_37491384 | MFNG | chr22 | 37464063 | 37491384 |
| HG03688 | hp2 | a0001 | c0001 | t0001 | g0009 | SAS | STU | MFNG_chr22_37464063_37491384 | MFNG | chr22 | 37464063 | 37491384 |
| HG03704 | hp1 | a0001 | c0001 | t0001 | g0003 | SAS | PJL | MFNG_chr22_37464063_37491384 | MFNG | chr22 | 37464063 | 37491384 |
| HG03704 | hp2 | a0001 | c0001 | t0001 | g0092 | SAS | PJL | MFNG_chr22_37464063_37491384 | MFNG | chr22 | 37464063 | 37491384 |
| HG03710 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | MFNG_chr22_37464063_37491384 | MFNG | chr22 | 37464063 | 37491384 |
| HG03710 | hp2 | a0001 | c0001 | t0001 | g0003 | SAS | PJL | MFNG_chr22_37464063_37491384 | MFNG | chr22 | 37464063 | 37491384 |
| HG03831 | hp1 | a0001 | c0001 | t0001 | g0004 | SAS | BEB | MFNG_chr22_37464063_37491384 | MFNG | chr22 | 37464063 | 37491384 |
| HG03831 | hp2 | a0001 | c0001 | t0001 | g0081 | SAS | BEB | MFNG_chr22_37464063_37491384 | MFNG | chr22 | 37464063 | 37491384 |
| HG03927 | hp1 | a0001 | c0001 | t0001 | g0050 | SAS | BEB | MFNG_chr22_37464063_37491384 | MFNG | chr22 | 37464063 | 37491384 |
| HG03927 | hp2 | a0001 | c0001 | t0001 | g0124 | SAS | BEB | MFNG_chr22_37464063_37491384 | MFNG | chr22 | 37464063 | 37491384 |
| HG04115 | hp1 | a0001 | c0001 | t0001 | g0004 | SAS | STU | MFNG_chr22_37464063_37491384 | MFNG | chr22 | 37464063 | 37491384 |
| HG04115 | hp2 | a0001 | c0001 | t0001 | g0138 | SAS | STU | MFNG_chr22_37464063_37491384 | MFNG | chr22 | 37464063 | 37491384 |
| HG04184 | hp1 | a0001 | c0001 | t0001 | g0084 | SAS | BEB | MFNG_chr22_37464063_37491384 | MFNG | chr22 | 37464063 | 37491384 |
| HG04184 | hp2 | a0001 | c0001 | t0001 | g0051 | SAS | BEB | MFNG_chr22_37464063_37491384 | MFNG | chr22 | 37464063 | 37491384 |
| HG04199 | hp1 | a0003 | c0006 | t0001 | g0058 | SAS | STU | MFNG_chr22_37464063_37491384 | MFNG | chr22 | 37464063 | 37491384 |
| HG04199 | hp2 | a0001 | c0001 | t0001 | g0009 | SAS | STU | MFNG_chr22_37464063_37491384 | MFNG | chr22 | 37464063 | 37491384 |
| HG04204 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | STU | MFNG_chr22_37464063_37491384 | MFNG | chr22 | 37464063 | 37491384 |
| HG04204 | hp2 | a0001 | c0001 | t0001 | g0003 | SAS | STU | MFNG_chr22_37464063_37491384 | MFNG | chr22 | 37464063 | 37491384 |
| HG04228 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | STU | MFNG_chr22_37464063_37491384 | MFNG | chr22 | 37464063 | 37491384 |
| HG04228 | hp2 | a0001 | c0001 | t0001 | g0002 | SAS | STU | MFNG_chr22_37464063_37491384 | MFNG | chr22 | 37464063 | 37491384 |
| NA18522 | hp1 | a0001 | c0001 | t0001 | g0120 | AFR | YRI | MFNG_chr22_37464063_37491384 | MFNG | chr22 | 37464063 | 37491384 |
| NA18522 | hp2 | a0001 | c0001 | t0001 | g0008 | AFR | YRI | MFNG_chr22_37464063_37491384 | MFNG | chr22 | 37464063 | 37491384 |
| NA18612 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CHB | MFNG_chr22_37464063_37491384 | MFNG | chr22 | 37464063 | 37491384 |
| NA18612 | hp2 | a0001 | c0001 | t0001 | g0133 | EAS | CHB | MFNG_chr22_37464063_37491384 | MFNG | chr22 | 37464063 | 37491384 |
| NA18906 | hp1 | a0001 | c0001 | t0001 | g0008 | AFR | YRI | MFNG_chr22_37464063_37491384 | MFNG | chr22 | 37464063 | 37491384 |
| NA18906 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | YRI | MFNG_chr22_37464063_37491384 | MFNG | chr22 | 37464063 | 37491384 |
| NA18939 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | MFNG_chr22_37464063_37491384 | MFNG | chr22 | 37464063 | 37491384 |
| NA18939 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | MFNG_chr22_37464063_37491384 | MFNG | chr22 | 37464063 | 37491384 |
| NA18942 | hp1 | a0001 | c0001 | t0001 | g0059 | EAS | JPT | MFNG_chr22_37464063_37491384 | MFNG | chr22 | 37464063 | 37491384 |
| NA18942 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | MFNG_chr22_37464063_37491384 | MFNG | chr22 | 37464063 | 37491384 |
| NA18943 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | MFNG_chr22_37464063_37491384 | MFNG | chr22 | 37464063 | 37491384 |
| NA18943 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | MFNG_chr22_37464063_37491384 | MFNG | chr22 | 37464063 | 37491384 |
| NA18944 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | MFNG_chr22_37464063_37491384 | MFNG | chr22 | 37464063 | 37491384 |
| NA18944 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | MFNG_chr22_37464063_37491384 | MFNG | chr22 | 37464063 | 37491384 |
| NA18945 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | MFNG_chr22_37464063_37491384 | MFNG | chr22 | 37464063 | 37491384 |
| NA18945 | hp2 | a0001 | c0001 | t0001 | g0038 | EAS | JPT | MFNG_chr22_37464063_37491384 | MFNG | chr22 | 37464063 | 37491384 |
| NA18946 | hp1 | a0001 | c0001 | t0001 | g0122 | EAS | JPT | MFNG_chr22_37464063_37491384 | MFNG | chr22 | 37464063 | 37491384 |
| NA18946 | hp2 | a0001 | c0001 | t0001 | g0077 | EAS | JPT | MFNG_chr22_37464063_37491384 | MFNG | chr22 | 37464063 | 37491384 |
| NA18948 | hp1 | a0001 | c0001 | t0001 | g0074 | EAS | JPT | MFNG_chr22_37464063_37491384 | MFNG | chr22 | 37464063 | 37491384 |
| NA18948 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | MFNG_chr22_37464063_37491384 | MFNG | chr22 | 37464063 | 37491384 |
| NA18951 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | MFNG_chr22_37464063_37491384 | MFNG | chr22 | 37464063 | 37491384 |
| NA18951 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | MFNG_chr22_37464063_37491384 | MFNG | chr22 | 37464063 | 37491384 |
| NA18952 | hp1 | a0001 | c0001 | t0001 | g0038 | EAS | JPT | MFNG_chr22_37464063_37491384 | MFNG | chr22 | 37464063 | 37491384 |
| NA18952 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | MFNG_chr22_37464063_37491384 | MFNG | chr22 | 37464063 | 37491384 |
| NA18956 | hp1 | a0001 | c0001 | t0001 | g0060 | EAS | JPT | MFNG_chr22_37464063_37491384 | MFNG | chr22 | 37464063 | 37491384 |
| NA18956 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | MFNG_chr22_37464063_37491384 | MFNG | chr22 | 37464063 | 37491384 |
| NA18957 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | MFNG_chr22_37464063_37491384 | MFNG | chr22 | 37464063 | 37491384 |
| NA18957 | hp2 | a0001 | c0001 | t0001 | g0142 | EAS | JPT | MFNG_chr22_37464063_37491384 | MFNG | chr22 | 37464063 | 37491384 |
| NA18959 | hp1 | a0001 | c0001 | t0001 | g0139 | EAS | JPT | MFNG_chr22_37464063_37491384 | MFNG | chr22 | 37464063 | 37491384 |
| NA18959 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | MFNG_chr22_37464063_37491384 | MFNG | chr22 | 37464063 | 37491384 |
| NA18960 | hp1 | a0001 | c0001 | t0001 | g0018 | EAS | JPT | MFNG_chr22_37464063_37491384 | MFNG | chr22 | 37464063 | 37491384 |
| NA18960 | hp2 | a0001 | c0007 | t0001 | g0046 | EAS | JPT | MFNG_chr22_37464063_37491384 | MFNG | chr22 | 37464063 | 37491384 |
| NA18964 | hp1 | a0001 | c0001 | t0001 | g0134 | EAS | JPT | MFNG_chr22_37464063_37491384 | MFNG | chr22 | 37464063 | 37491384 |
| NA18964 | hp2 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | MFNG_chr22_37464063_37491384 | MFNG | chr22 | 37464063 | 37491384 |
| NA18965 | hp1 | a0001 | c0001 | t0001 | g0123 | EAS | JPT | MFNG_chr22_37464063_37491384 | MFNG | chr22 | 37464063 | 37491384 |
| NA18965 | hp2 | a0001 | c0001 | t0001 | g0140 | EAS | JPT | MFNG_chr22_37464063_37491384 | MFNG | chr22 | 37464063 | 37491384 |
| NA18966 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | MFNG_chr22_37464063_37491384 | MFNG | chr22 | 37464063 | 37491384 |
| NA18966 | hp2 | a0001 | c0001 | t0001 | g0061 | EAS | JPT | MFNG_chr22_37464063_37491384 | MFNG | chr22 | 37464063 | 37491384 |
| NA18969 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | MFNG_chr22_37464063_37491384 | MFNG | chr22 | 37464063 | 37491384 |
| NA18969 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | MFNG_chr22_37464063_37491384 | MFNG | chr22 | 37464063 | 37491384 |
| NA18971 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | MFNG_chr22_37464063_37491384 | MFNG | chr22 | 37464063 | 37491384 |
| NA18971 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | MFNG_chr22_37464063_37491384 | MFNG | chr22 | 37464063 | 37491384 |
| NA18973 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | MFNG_chr22_37464063_37491384 | MFNG | chr22 | 37464063 | 37491384 |
| NA18973 | hp2 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | MFNG_chr22_37464063_37491384 | MFNG | chr22 | 37464063 | 37491384 |
| NA18977 | hp1 | a0001 | c0001 | t0001 | g0082 | EAS | JPT | MFNG_chr22_37464063_37491384 | MFNG | chr22 | 37464063 | 37491384 |
| NA18977 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | MFNG_chr22_37464063_37491384 | MFNG | chr22 | 37464063 | 37491384 |
| NA18979 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | MFNG_chr22_37464063_37491384 | MFNG | chr22 | 37464063 | 37491384 |
| NA18979 | hp2 | a0001 | c0001 | t0001 | g0023 | EAS | JPT | MFNG_chr22_37464063_37491384 | MFNG | chr22 | 37464063 | 37491384 |
| NA18980 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | MFNG_chr22_37464063_37491384 | MFNG | chr22 | 37464063 | 37491384 |
| NA18980 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | MFNG_chr22_37464063_37491384 | MFNG | chr22 | 37464063 | 37491384 |
| NA18982 | hp1 | a0001 | c0001 | t0001 | g0031 | EAS | JPT | MFNG_chr22_37464063_37491384 | MFNG | chr22 | 37464063 | 37491384 |
| NA18982 | hp2 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | MFNG_chr22_37464063_37491384 | MFNG | chr22 | 37464063 | 37491384 |
| NA18983 | hp1 | a0001 | c0001 | t0001 | g0048 | EAS | JPT | MFNG_chr22_37464063_37491384 | MFNG | chr22 | 37464063 | 37491384 |
| NA18983 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | MFNG_chr22_37464063_37491384 | MFNG | chr22 | 37464063 | 37491384 |
| NA18986 | hp1 | a0001 | c0001 | t0001 | g0032 | EAS | JPT | MFNG_chr22_37464063_37491384 | MFNG | chr22 | 37464063 | 37491384 |
| NA18986 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | MFNG_chr22_37464063_37491384 | MFNG | chr22 | 37464063 | 37491384 |
| NA18990 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | MFNG_chr22_37464063_37491384 | MFNG | chr22 | 37464063 | 37491384 |
| NA18990 | hp2 | a0001 | c0001 | t0001 | g0018 | EAS | JPT | MFNG_chr22_37464063_37491384 | MFNG | chr22 | 37464063 | 37491384 |
| NA18993 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | MFNG_chr22_37464063_37491384 | MFNG | chr22 | 37464063 | 37491384 |
| NA18993 | hp2 | a0001 | c0001 | t0001 | g0075 | EAS | JPT | MFNG_chr22_37464063_37491384 | MFNG | chr22 | 37464063 | 37491384 |
| NA18997 | hp1 | a0001 | c0001 | t0001 | g0107 | EAS | JPT | MFNG_chr22_37464063_37491384 | MFNG | chr22 | 37464063 | 37491384 |
| NA18997 | hp2 | a0001 | c0001 | t0001 | g0031 | EAS | JPT | MFNG_chr22_37464063_37491384 | MFNG | chr22 | 37464063 | 37491384 |
| NA19003 | hp1 | a0001 | c0001 | t0001 | g0106 | EAS | JPT | MFNG_chr22_37464063_37491384 | MFNG | chr22 | 37464063 | 37491384 |
| NA19003 | hp2 | a0001 | c0001 | t0001 | g0041 | EAS | JPT | MFNG_chr22_37464063_37491384 | MFNG | chr22 | 37464063 | 37491384 |
| NA19005 | hp1 | a0001 | c0001 | t0002 | g0068 | EAS | JPT | MFNG_chr22_37464063_37491384 | MFNG | chr22 | 37464063 | 37491384 |
| NA19005 | hp2 | a0001 | c0001 | t0001 | g0083 | EAS | JPT | MFNG_chr22_37464063_37491384 | MFNG | chr22 | 37464063 | 37491384 |
| NA19043 | hp1 | a0001 | c0001 | t0001 | g0054 | AFR | LWK | MFNG_chr22_37464063_37491384 | MFNG | chr22 | 37464063 | 37491384 |
| NA19043 | hp2 | a0001 | c0001 | t0001 | g0088 | AFR | LWK | MFNG_chr22_37464063_37491384 | MFNG | chr22 | 37464063 | 37491384 |
| NA19056 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | MFNG_chr22_37464063_37491384 | MFNG | chr22 | 37464063 | 37491384 |
| NA19056 | hp2 | a0001 | c0001 | t0001 | g0129 | EAS | JPT | MFNG_chr22_37464063_37491384 | MFNG | chr22 | 37464063 | 37491384 |
| NA19057 | hp1 | a0001 | c0001 | t0001 | g0045 | EAS | JPT | MFNG_chr22_37464063_37491384 | MFNG | chr22 | 37464063 | 37491384 |
| NA19057 | hp2 | a0001 | c0001 | t0001 | g0032 | EAS | JPT | MFNG_chr22_37464063_37491384 | MFNG | chr22 | 37464063 | 37491384 |
| NA19058 | hp1 | a0004 | c0005 | t0001 | g0076 | EAS | JPT | MFNG_chr22_37464063_37491384 | MFNG | chr22 | 37464063 | 37491384 |
| NA19058 | hp2 | a0001 | c0001 | t0001 | g0014 | EAS | JPT | MFNG_chr22_37464063_37491384 | MFNG | chr22 | 37464063 | 37491384 |
| NA19060 | hp1 | a0001 | c0001 | t0001 | g0098 | EAS | JPT | MFNG_chr22_37464063_37491384 | MFNG | chr22 | 37464063 | 37491384 |
| NA19060 | hp2 | a0001 | c0001 | t0001 | g0143 | EAS | JPT | MFNG_chr22_37464063_37491384 | MFNG | chr22 | 37464063 | 37491384 |
| NA19064 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | MFNG_chr22_37464063_37491384 | MFNG | chr22 | 37464063 | 37491384 |
| NA19064 | hp2 | a0001 | c0001 | t0001 | g0014 | EAS | JPT | MFNG_chr22_37464063_37491384 | MFNG | chr22 | 37464063 | 37491384 |
| NA19066 | hp1 | a0001 | c0001 | t0001 | g0136 | EAS | JPT | MFNG_chr22_37464063_37491384 | MFNG | chr22 | 37464063 | 37491384 |
| NA19066 | hp2 | a0001 | c0001 | t0001 | g0022 | EAS | JPT | MFNG_chr22_37464063_37491384 | MFNG | chr22 | 37464063 | 37491384 |
| NA19084 | hp1 | a0001 | c0001 | t0001 | g0141 | EAS | JPT | MFNG_chr22_37464063_37491384 | MFNG | chr22 | 37464063 | 37491384 |
| NA19084 | hp2 | a0001 | c0001 | t0001 | g0034 | EAS | JPT | MFNG_chr22_37464063_37491384 | MFNG | chr22 | 37464063 | 37491384 |
| NA19087 | hp1 | a0001 | c0001 | t0001 | g0131 | EAS | JPT | MFNG_chr22_37464063_37491384 | MFNG | chr22 | 37464063 | 37491384 |
| NA19087 | hp2 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | MFNG_chr22_37464063_37491384 | MFNG | chr22 | 37464063 | 37491384 |
| NA19088 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | MFNG_chr22_37464063_37491384 | MFNG | chr22 | 37464063 | 37491384 |
| NA19088 | hp2 | a0001 | c0001 | t0001 | g0052 | EAS | JPT | MFNG_chr22_37464063_37491384 | MFNG | chr22 | 37464063 | 37491384 |
| NA19091 | hp1 | a0001 | c0001 | t0001 | g0023 | EAS | JPT | MFNG_chr22_37464063_37491384 | MFNG | chr22 | 37464063 | 37491384 |
| NA19091 | hp2 | a0001 | c0001 | t0001 | g0022 | EAS | JPT | MFNG_chr22_37464063_37491384 | MFNG | chr22 | 37464063 | 37491384 |
| NA19240 | hp1 | a0001 | c0001 | t0001 | g0086 | AFR | YRI | MFNG_chr22_37464063_37491384 | MFNG | chr22 | 37464063 | 37491384 |
| NA19240 | hp2 | a0001 | c0001 | t0001 | g0110 | AFR | YRI | MFNG_chr22_37464063_37491384 | MFNG | chr22 | 37464063 | 37491384 |
| NA20129 | hp1 | a0001 | c0001 | t0001 | g0043 | AFR | ASW | MFNG_chr22_37464063_37491384 | MFNG | chr22 | 37464063 | 37491384 |
| NA20129 | hp2 | a0001 | c0001 | t0001 | g0126 | AFR | ASW | MFNG_chr22_37464063_37491384 | MFNG | chr22 | 37464063 | 37491384 |
| NA20752 | hp1 | a0001 | c0001 | t0001 | g0008 | EUR | TSI | MFNG_chr22_37464063_37491384 | MFNG | chr22 | 37464063 | 37491384 |
| NA20752 | hp2 | a0001 | c0001 | t0001 | g0001 | EUR | TSI | MFNG_chr22_37464063_37491384 | MFNG | chr22 | 37464063 | 37491384 |
| NA20905 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | GIH | MFNG_chr22_37464063_37491384 | MFNG | chr22 | 37464063 | 37491384 |
| NA20905 | hp2 | a0001 | c0001 | t0001 | g0003 | SAS | GIH | MFNG_chr22_37464063_37491384 | MFNG | chr22 | 37464063 | 37491384 |
| HG02109 | hp1 | a0001 | c0001 | t0001 | g0066 | AFR | ACB | MFNG_chr22_37464063_37491384 | MFNG | chr22 | 37464063 | 37491384 |
| HG02109 | hp2 | a0001 | c0001 | t0001 | g0057 | AFR | ACB | MFNG_chr22_37464063_37491384 | MFNG | chr22 | 37464063 | 37491384 |
| HG02486 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | ACB | MFNG_chr22_37464063_37491384 | MFNG | chr22 | 37464063 | 37491384 |
| HG02486 | hp2 | a0002 | c0003 | t0001 | g0039 | AFR | ACB | MFNG_chr22_37464063_37491384 | MFNG | chr22 | 37464063 | 37491384 |
| HG02559 | hp1 | a0001 | c0001 | t0001 | g0104 | AFR | ACB | MFNG_chr22_37464063_37491384 | MFNG | chr22 | 37464063 | 37491384 |
| HG02559 | hp2 | a0001 | c0001 | t0001 | g0013 | AFR | ACB | MFNG_chr22_37464063_37491384 | MFNG | chr22 | 37464063 | 37491384 |
| HG03471 | hp1 | a0001 | c0001 | t0001 | g0113 | AFR | MSL | MFNG_chr22_37464063_37491384 | MFNG | chr22 | 37464063 | 37491384 |
| HG03471 | hp2 | a0001 | c0001 | t0001 | g0008 | AFR | MSL | MFNG_chr22_37464063_37491384 | MFNG | chr22 | 37464063 | 37491384 |
| NA20300 | hp1 | a0001 | c0001 | t0001 | g0030 | AFR | USA | MFNG_chr22_37464063_37491384 | MFNG | chr22 | 37464063 | 37491384 |
| NA20300 | hp2 | a0001 | c0001 | t0001 | g0036 | AFR | USA | MFNG_chr22_37464063_37491384 | MFNG | chr22 | 37464063 | 37491384 |
| NA21309 | hp1 | a0001 | c0001 | t0001 | g0013 | AFR | LWK | MFNG_chr22_37464063_37491384 | MFNG | chr22 | 37464063 | 37491384 |
| NA21309 | hp2 | a0005 | c0004 | t0001 | g0080 | AFR | LWK | MFNG_chr22_37464063_37491384 | MFNG | chr22 | 37464063 | 37491384 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0001 | g0137 | REF | REF | MFNG_chr22_37464063_37491384 | MFNG | chr22 | 37464063 | 37491384 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0001 | g0001 | REF | REF | MFNG_chr22_37464063_37491384 | MFNG | chr22 | 37464063 | 37491384 |
| view | chr:pos | ref | alt | # # of ahapid:amino-acid(protein) level |
ahapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr22:37469997 | T | C | 1 | a0004 | 1 | NA19058.hp1 | missense_variant | MODERATE | c.932A>G | p.Asp311Gly | MFNG | ENSG00000100060.18 | transcript | ENST00000356998.8 | protein_coding | 8/8 | 1139/2073 | 932/966 | 311/321 | chr22 | 37469997 | |||
| chr22:37472461 | G | A | 1 | a0003 | 1 | HG04199.hp1 | missense_variant | MODERATE | c.881C>T | p.Pro294Leu | MFNG | ENSG00000100060.18 | transcript | ENST00000356998.8 | protein_coding | 7/8 | 1088/2073 | 881/966 | 294/321 | chr22 | 37472461 | |||
| chr22:37474669 | C | T | 1 | a0005 | 1 | NA21309.hp2 | missense_variant | MODERATE | c.656G>A | p.Arg219His | MFNG | ENSG00000100060.18 | transcript | ENST00000356998.8 | protein_coding | 6/8 | 863/2073 | 656/966 | 219/321 | chr22 | 37474669 | |||
| chr22:37486111 | A | C | 1 | a0002 | 1 | HG02486.hp2 | missense_variant | MODERATE | c.67T>G | p.Cys23Gly | MFNG | ENSG00000100060.18 | transcript | ENST00000356998.8 | protein_coding | 1/8 | 274/2073 | 67/966 | 23/321 | chr22 | 37486111 |
| view | chr:pos | ref | alt | # # of chapid |
chapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr22:37474575 | G | A | 1 | a0001c0007 | 1 | NA18960.hp2 | synonymous_variant | LOW | c.750C>T | p.Ser250Ser | MFNG | ENSG00000100060.18 | transcript | ENST00000356998.8 | protein_coding | 6/8 | 957/2073 | 750/966 | 250/321 | chr22 | 37474575 | |||
| chr22:37474593 | G | A | 1 | a0002c0003 | 1 | HG02486.hp2 | synonymous_variant | LOW | c.732C>T | p.Gly244Gly | MFNG | ENSG00000100060.18 | transcript | ENST00000356998.8 | protein_coding | 6/8 | 939/2073 | 732/966 | 244/321 | chr22 | 37474593 | |||
| chr22:37479408 | A | G | 1 | a0001c0002 | 3 | HG03098.hp2 HG03453.hp2 HG03516.hp1 |
synonymous_variant | LOW | c.498T>C | p.Tyr166Tyr | MFNG | ENSG00000100060.18 | transcript | ENST00000356998.8 | protein_coding | 4/8 | 705/2073 | 498/966 | 166/321 | chr22 | 37479408 | |||
| chr22:37486019 | T | G | 1 | a0001c0008 | 1 | HG02622.hp1 | synonymous_variant | LOW | c.159A>C | p.Leu53Leu | MFNG | ENSG00000100060.18 | transcript | ENST00000356998.8 | protein_coding | 1/8 | 366/2073 | 159/966 | 53/321 | chr22 | 37486019 |
| view | chr:pos | ref | alt | # # of thapid:transcript level |
thapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr22:37469196 | T | A | 2 | a0001c0001t0001 a0002c0003t0001 |
6 | HG01109.hp2 HG02486.hp2 HG02976.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*767A>T | MFNG | ENSG00000100060.18 | transcript | ENST00000356998.8 | protein_coding | 8/8 | 767 | chr22 | 37469196 | ||||||
| chr22:37469360 | T | C | 1 | a0001c0001t0001 | 1 | NA20300.hp2 | 3_prime_UTR_variant | MODIFIER | c.*603A>G | MFNG | ENSG00000100060.18 | transcript | ENST00000356998.8 | protein_coding | 8/8 | 603 | chr22 | 37469360 | ||||||
| chr22:37469416 | C | T | 1 | a0001c0008t0001 | 1 | HG02622.hp1 | 3_prime_UTR_variant | MODIFIER | c.*547G>A | MFNG | ENSG00000100060.18 | transcript | ENST00000356998.8 | protein_coding | 8/8 | 547 | chr22 | 37469416 | ||||||
| chr22:37469522 | C | T | 1 | a0001c0001t0001 | 1 | HG00323.hp1 | 3_prime_UTR_variant | MODIFIER | c.*441G>A | MFNG | ENSG00000100060.18 | transcript | ENST00000356998.8 | protein_coding | 8/8 | 441 | chr22 | 37469522 | ||||||
| chr22:37469553 | G | A | 1 | a0001c0001t0001 | 1 | HG03490.hp1 | 3_prime_UTR_variant | MODIFIER | c.*410C>T | MFNG | ENSG00000100060.18 | transcript | ENST00000356998.8 | protein_coding | 8/8 | 410 | chr22 | 37469553 |
| view | chr:pos | ref | alt | # # of ghapid:genebody level |
ghapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | genebody_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr22:37470064 | C | T | 1 | a0001c0001t0001g0060 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.900-35G>A | MFNG | ENSG00000100060.18 | transcript | ENST00000356998.8 | protein_coding | 7/7 | chr22 | 37470064 | |||||||
| chr22:37470296 | C | A | 2 | a0001c0001t0001g0008 a0001c0001t0001g0126 |
6 | HG02886.hp2 HG03471.hp2 NA18522.hp2 others(3): Show |
intron_variant | MODIFIER | c.900-267G>T | MFNG | ENSG00000100060.18 | transcript | ENST00000356998.8 | protein_coding | 7/7 | chr22 | 37470296 | |||||||
| chr22:37470297 | G | A | 2 | a0001c0001t0001g0052 a0001c0001t0001g0078 |
2 | HG02080.hp1 NA19088.hp2 |
intron_variant | MODIFIER | c.900-268C>T | MFNG | ENSG00000100060.18 | transcript | ENST00000356998.8 | protein_coding | 7/7 | chr22 | 37470297 | |||||||
| chr22:37470460 | T | C | 1 | a0001c0001t0001g0055 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.900-431A>G | MFNG | ENSG00000100060.18 | transcript | ENST00000356998.8 | protein_coding | 7/7 | chr22 | 37470460 | |||||||
| chr22:37470770 | C | G | 1 | a0001c0002t0001g0044 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.900-741G>C | MFNG | ENSG00000100060.18 | transcript | ENST00000356998.8 | protein_coding | 7/7 | chr22 | 37470770 | |||||||
| chr22:37470983 | G | C | 1 | a0001c0002t0001g0044 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.900-954C>G | MFNG | ENSG00000100060.18 | transcript | ENST00000356998.8 | protein_coding | 7/7 | chr22 | 37470983 | |||||||
| chr22:37470991 | A | G | 1 | a0001c0002t0001g0044 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.900-962T>C | MFNG | ENSG00000100060.18 | transcript | ENST00000356998.8 | protein_coding | 7/7 | chr22 | 37470991 | |||||||
| chr22:37471508 | C | T | 1 | a0001c0001t0001g0021 | 2 | HG01496.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.899+935G>A | MFNG | ENSG00000100060.18 | transcript | ENST00000356998.8 | protein_coding | 7/7 | chr22 | 37471508 | |||||||
| chr22:37471509 | C | A | 1 | a0001c0001t0001g0128 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.899+934G>T | MFNG | ENSG00000100060.18 | transcript | ENST00000356998.8 | protein_coding | 7/7 | chr22 | 37471509 | |||||||
| chr22:37471522 | C | T | 1 | a0003c0006t0001g0058 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.899+921G>A | MFNG | ENSG00000100060.18 | transcript | ENST00000356998.8 | protein_coding | 7/7 | chr22 | 37471522 | |||||||
| chr22:37471539 | G | A | 1 | a0001c0001t0001g0056 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.899+904C>T | MFNG | ENSG00000100060.18 | transcript | ENST00000356998.8 | protein_coding | 7/7 | chr22 | 37471539 | |||||||
| chr22:37471553 | G | A | 1 | a0001c0008t0001g0144 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.899+890C>T | MFNG | ENSG00000100060.18 | transcript | ENST00000356998.8 | protein_coding | 7/7 | chr22 | 37471553 | |||||||
| chr22:37471697 | G | T | 1 | a0001c0001t0001g0101 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.899+746C>A | MFNG | ENSG00000100060.18 | transcript | ENST00000356998.8 | protein_coding | 7/7 | chr22 | 37471697 | |||||||
| chr22:37471747 | T | C | 1 | a0001c0001t0001g0021 | 2 | HG01496.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.899+696A>G | MFNG | ENSG00000100060.18 | transcript | ENST00000356998.8 | protein_coding | 7/7 | chr22 | 37471747 | |||||||
| chr22:37471821 | G | A | 7 | a0001c0001t0001g0096 a0001c0001t0001g0097 a0001c0001t0001g0099 others(4): Show |
7 | HG01109.hp2 HG02622.hp1 HG02976.hp2 others(4): Show |
intron_variant | MODIFIER | c.899+622C>T | MFNG | ENSG00000100060.18 | transcript | ENST00000356998.8 | protein_coding | 7/7 | chr22 | 37471821 | |||||||
| chr22:37471830 | C | CA | 60 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(57): Show |
119 | HG00323.hp2 HG00544.hp1 HG00558.hp1 others(116): Show |
intron_variant | MODIFIER | c.899+612dupT | MFNG | ENSG00000100060.18 | transcript | ENST00000356998.8 | protein_coding | 7/7 | chr22 | 37471830 | |||||||
| chr22:37471830 | C | CAA | 19 | a0001c0001t0001g0014 a0001c0001t0001g0018 a0001c0001t0001g0026 others(16): Show |
29 | HG00438.hp1 HG00621.hp2 HG00735.hp2 others(26): Show |
intron_variant | MODIFIER | c.899+611_899+612dup others(2): Show |
MFNG | ENSG00000100060.18 | transcript | ENST00000356998.8 | protein_coding | 7/7 | chr22 | 37471830 | |||||||
| chr22:37471830 | C | CAAA | 9 | a0001c0001t0001g0057 a0001c0001t0001g0066 a0001c0001t0001g0091 others(6): Show |
10 | HG00741.hp2 HG01109.hp2 HG02109.hp1 others(7): Show |
intron_variant | MODIFIER | c.899+610_899+612dup others(3): Show |
MFNG | ENSG00000100060.18 | transcript | ENST00000356998.8 | protein_coding | 7/7 | chr22 | 37471830 | |||||||
| chr22:37471830 | CA | C | 3 | a0001c0001t0001g0009 a0001c0001t0001g0033 a0001c0001t0001g0054 |
7 | HG01256.hp2 HG01258.hp1 HG02622.hp2 others(4): Show |
intron_variant | MODIFIER | c.899+612delT | MFNG | ENSG00000100060.18 | transcript | ENST00000356998.8 | protein_coding | 7/7 | chr22 | 37471830 | |||||||
| chr22:37471964 | G | A | 1 | a0001c0001t0001g0102 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.899+479C>T | MFNG | ENSG00000100060.18 | transcript | ENST00000356998.8 | protein_coding | 7/7 | chr22 | 37471964 | |||||||
| chr22:37472016 | T | C | 1 | a0001c0002t0001g0025 | 2 | HG03098.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.899+427A>G | MFNG | ENSG00000100060.18 | transcript | ENST00000356998.8 | protein_coding | 7/7 | chr22 | 37472016 | |||||||
| chr22:37472109 | C | T | 1 | a0001c0001t0001g0053 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.899+334G>A | MFNG | ENSG00000100060.18 | transcript | ENST00000356998.8 | protein_coding | 7/7 | chr22 | 37472109 | |||||||
| chr22:37472110 | G | A | 1 | a0001c0001t0001g0085 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.899+333C>T | MFNG | ENSG00000100060.18 | transcript | ENST00000356998.8 | protein_coding | 7/7 | chr22 | 37472110 | |||||||
| chr22:37472132 | A | G | 3 | a0001c0001t0001g0052 a0001c0001t0001g0078 a0001c0001t0001g0079 |
3 | HG00408.hp1 HG02080.hp1 NA19088.hp2 |
intron_variant | MODIFIER | c.899+311T>C | MFNG | ENSG00000100060.18 | transcript | ENST00000356998.8 | protein_coding | 7/7 | chr22 | 37472132 | |||||||
| chr22:37472759 | G | C | 1 | a0001c0001t0001g0030 | 2 | HG02258.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.814-231C>G | MFNG | ENSG00000100060.18 | transcript | ENST00000356998.8 | protein_coding | 6/7 | chr22 | 37472759 | |||||||
| chr22:37472993 | G | C | 2 | a0001c0001t0001g0139 a0001c0001t0001g0140 |
2 | NA18959.hp1 NA18965.hp2 |
intron_variant | MODIFIER | c.814-465C>G | MFNG | ENSG00000100060.18 | transcript | ENST00000356998.8 | protein_coding | 6/7 | chr22 | 37472993 | |||||||
| chr22:37473063 | G | A | 1 | a0001c0001t0001g0022 | 2 | NA19066.hp2 NA19091.hp2 |
intron_variant | MODIFIER | c.814-535C>T | MFNG | ENSG00000100060.18 | transcript | ENST00000356998.8 | protein_coding | 6/7 | chr22 | 37473063 | |||||||
| chr22:37473093 | G | A | 22 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0014 others(19): Show |
43 | HG00609.hp1 HG00621.hp1 HG00639.hp1 others(40): Show |
intron_variant | MODIFIER | c.814-565C>T | MFNG | ENSG00000100060.18 | transcript | ENST00000356998.8 | protein_coding | 6/7 | chr22 | 37473093 | |||||||
| chr22:37473165 | C | T | 1 | a0001c0001t0001g0051 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.814-637G>A | MFNG | ENSG00000100060.18 | transcript | ENST00000356998.8 | protein_coding | 6/7 | chr22 | 37473165 | |||||||
| chr22:37473307 | T | C | 1 | a0001c0001t0001g0030 | 2 | HG02258.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.814-779A>G | MFNG | ENSG00000100060.18 | transcript | ENST00000356998.8 | protein_coding | 6/7 | chr22 | 37473307 | |||||||
| chr22:37473383 | C | T | 35 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0011 others(32): Show |
73 | HG00323.hp2 HG00438.hp1 HG00544.hp1 others(70): Show |
intron_variant | MODIFIER | c.814-855G>A | MFNG | ENSG00000100060.18 | transcript | ENST00000356998.8 | protein_coding | 6/7 | chr22 | 37473383 | |||||||
| chr22:37473442 | A | G | 7 | a0001c0001t0001g0010 a0001c0001t0001g0015 a0001c0001t0001g0086 others(4): Show |
12 | HG00639.hp2 HG00642.hp2 HG01167.hp1 others(9): Show |
intron_variant | MODIFIER | c.814-914T>C | MFNG | ENSG00000100060.18 | transcript | ENST00000356998.8 | protein_coding | 6/7 | chr22 | 37473442 | |||||||
| chr22:37473495 | C | T | 1 | a0001c0001t0001g0050 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.814-967G>A | MFNG | ENSG00000100060.18 | transcript | ENST00000356998.8 | protein_coding | 6/7 | chr22 | 37473495 | |||||||
| chr22:37473513 | TTGGGCTG others(7): Show |
T | 1 | a0001c0001t0001g0090 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.813+985_814-986del others(14): Show |
MFNG | ENSG00000100060.18 | transcript | ENST00000356998.8 | protein_coding | 6/7 | chr22 | 37473513 | |||||||
| chr22:37473562 | C | G | 1 | a0001c0001t0001g0049 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.813+950G>C | MFNG | ENSG00000100060.18 | transcript | ENST00000356998.8 | protein_coding | 6/7 | chr22 | 37473562 | |||||||
| chr22:37473661 | T | C | 1 | a0001c0001t0001g0062 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.813+851A>G | MFNG | ENSG00000100060.18 | transcript | ENST00000356998.8 | protein_coding | 6/7 | chr22 | 37473661 | |||||||
| chr22:37473887 | C | T | 1 | a0001c0002t0001g0044 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.813+625G>A | MFNG | ENSG00000100060.18 | transcript | ENST00000356998.8 | protein_coding | 6/7 | chr22 | 37473887 | |||||||
| chr22:37473919 | G | A | 1 | a0001c0002t0001g0044 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.813+593C>T | MFNG | ENSG00000100060.18 | transcript | ENST00000356998.8 | protein_coding | 6/7 | chr22 | 37473919 | |||||||
| chr22:37474016 | G | A | 2 | a0001c0002t0001g0044 a0001c0008t0001g0144 |
2 | HG02622.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.813+496C>T | MFNG | ENSG00000100060.18 | transcript | ENST00000356998.8 | protein_coding | 6/7 | chr22 | 37474016 | |||||||
| chr22:37474053 | G | T | 1 | a0001c0001t0001g0136 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.813+459C>A | MFNG | ENSG00000100060.18 | transcript | ENST00000356998.8 | protein_coding | 6/7 | chr22 | 37474053 | |||||||
| chr22:37474148 | G | A | 11 | a0001c0001t0001g0006 a0001c0001t0001g0011 a0001c0001t0001g0033 others(8): Show |
20 | HG01109.hp1 HG01243.hp2 HG02055.hp1 others(17): Show |
intron_variant | MODIFIER | c.813+364C>T | MFNG | ENSG00000100060.18 | transcript | ENST00000356998.8 | protein_coding | 6/7 | chr22 | 37474148 | |||||||
| chr22:37474247 | T | C | 1 | a0001c0008t0001g0144 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.813+265A>G | MFNG | ENSG00000100060.18 | transcript | ENST00000356998.8 | protein_coding | 6/7 | chr22 | 37474247 | |||||||
| chr22:37474390 | T | C | 1 | a0001c0002t0001g0044 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.813+122A>G | MFNG | ENSG00000100060.18 | transcript | ENST00000356998.8 | protein_coding | 6/7 | chr22 | 37474390 | |||||||
| chr22:37474733 | G | A | 22 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0014 others(19): Show |
42 | HG00609.hp1 HG00621.hp1 HG00741.hp2 others(39): Show |
intron_variant | MODIFIER | c.648-56C>T | MFNG | ENSG00000100060.18 | transcript | ENST00000356998.8 | protein_coding | 5/7 | chr22 | 37474733 | |||||||
| chr22:37474836 | C | G | 2 | a0001c0001t0001g0071 a0001c0001t0001g0072 |
2 | HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.648-159G>C | MFNG | ENSG00000100060.18 | transcript | ENST00000356998.8 | protein_coding | 5/7 | chr22 | 37474836 | |||||||
| chr22:37475130 | G | C | 5 | a0001c0001t0001g0096 a0001c0001t0001g0097 a0001c0001t0001g0099 others(2): Show |
5 | HG01109.hp2 HG02976.hp2 HG03225.hp2 others(2): Show |
intron_variant | MODIFIER | c.648-453C>G | MFNG | ENSG00000100060.18 | transcript | ENST00000356998.8 | protein_coding | 5/7 | chr22 | 37475130 | |||||||
| chr22:37475247 | A | C | 1 | a0001c0001t0001g0097 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.648-570T>G | MFNG | ENSG00000100060.18 | transcript | ENST00000356998.8 | protein_coding | 5/7 | chr22 | 37475247 | |||||||
| chr22:37475309 | C | T | 2 | a0001c0001t0001g0071 a0001c0001t0001g0072 |
2 | HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.648-632G>A | MFNG | ENSG00000100060.18 | transcript | ENST00000356998.8 | protein_coding | 5/7 | chr22 | 37475309 | |||||||
| chr22:37475385 | G | A | 1 | a0001c0002t0001g0025 | 2 | HG03098.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.648-708C>T | MFNG | ENSG00000100060.18 | transcript | ENST00000356998.8 | protein_coding | 5/7 | chr22 | 37475385 | |||||||
| chr22:37475602 | G | A | 2 | a0001c0001t0001g0062 a0005c0004t0001g0080 |
2 | HG03041.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.648-925C>T | MFNG | ENSG00000100060.18 | transcript | ENST00000356998.8 | protein_coding | 5/7 | chr22 | 37475602 | |||||||
| chr22:37475826 | C | T | 18 | a0001c0001t0001g0016 a0001c0001t0001g0028 a0001c0001t0001g0029 others(15): Show |
23 | HG00735.hp2 HG00741.hp1 HG01099.hp2 others(20): Show |
intron_variant | MODIFIER | c.647+1070G>A | MFNG | ENSG00000100060.18 | transcript | ENST00000356998.8 | protein_coding | 5/7 | chr22 | 37475826 | |||||||
| chr22:37475845 | C | A | 1 | a0001c0001t0001g0103 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.647+1051G>T | MFNG | ENSG00000100060.18 | transcript | ENST00000356998.8 | protein_coding | 5/7 | chr22 | 37475845 | |||||||
| chr22:37475853 | T | C | 2 | a0001c0001t0001g0062 a0005c0004t0001g0080 |
2 | HG03041.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.647+1043A>G | MFNG | ENSG00000100060.18 | transcript | ENST00000356998.8 | protein_coding | 5/7 | chr22 | 37475853 | |||||||
| chr22:37476029 | C | T | 1 | a0001c0008t0001g0144 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.647+867G>A | MFNG | ENSG00000100060.18 | transcript | ENST00000356998.8 | protein_coding | 5/7 | chr22 | 37476029 | |||||||
| chr22:37476086 | T | C | 1 | a0001c0002t0001g0044 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.647+810A>G | MFNG | ENSG00000100060.18 | transcript | ENST00000356998.8 | protein_coding | 5/7 | chr22 | 37476086 | |||||||
| chr22:37476224 | G | A | 1 | a0001c0001t0001g0063 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.647+672C>T | MFNG | ENSG00000100060.18 | transcript | ENST00000356998.8 | protein_coding | 5/7 | chr22 | 37476224 | |||||||
| chr22:37476537 | C | A | 1 | a0001c0002t0001g0044 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.647+359G>T | MFNG | ENSG00000100060.18 | transcript | ENST00000356998.8 | protein_coding | 5/7 | chr22 | 37476537 | |||||||
| chr22:37476585 | A | G | 1 | a0001c0001t0001g0020 | 2 | HG01884.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.647+311T>C | MFNG | ENSG00000100060.18 | transcript | ENST00000356998.8 | protein_coding | 5/7 | chr22 | 37476585 | |||||||
| chr22:37476614 | T | C | 1 | a0001c0001t0001g0079 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.647+282A>G | MFNG | ENSG00000100060.18 | transcript | ENST00000356998.8 | protein_coding | 5/7 | chr22 | 37476614 | |||||||
| chr22:37476643 | G | A | 1 | a0001c0008t0001g0144 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.647+253C>T | MFNG | ENSG00000100060.18 | transcript | ENST00000356998.8 | protein_coding | 5/7 | chr22 | 37476643 | |||||||
| chr22:37476714 | A | G | 1 | a0001c0002t0001g0044 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.647+182T>C | MFNG | ENSG00000100060.18 | transcript | ENST00000356998.8 | protein_coding | 5/7 | chr22 | 37476714 | |||||||
| chr22:37476984 | G | A | 1 | a0001c0008t0001g0144 | 1 | HG02622.hp1 | splice_region_variant&intron_variant | LOW | c.562-3C>T | MFNG | ENSG00000100060.18 | transcript | ENST00000356998.8 | protein_coding | 4/7 | chr22 | 37476984 | |||||||
| chr22:37477376 | G | A | 1 | a0001c0001t0001g0108 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.562-395C>T | MFNG | ENSG00000100060.18 | transcript | ENST00000356998.8 | protein_coding | 4/7 | chr22 | 37477376 | |||||||
| chr22:37477489 | C | A | 1 | a0001c0001t0001g0072 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.562-508G>T | MFNG | ENSG00000100060.18 | transcript | ENST00000356998.8 | protein_coding | 4/7 | chr22 | 37477489 | |||||||
| chr22:37477490 | A | G | 1 | a0001c0001t0001g0072 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.562-509T>C | MFNG | ENSG00000100060.18 | transcript | ENST00000356998.8 | protein_coding | 4/7 | chr22 | 37477490 | |||||||
| chr22:37477492 | G | C | 1 | a0001c0001t0001g0072 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.562-511C>G | MFNG | ENSG00000100060.18 | transcript | ENST00000356998.8 | protein_coding | 4/7 | chr22 | 37477492 | |||||||
| chr22:37477592 | G | A | 6 | a0001c0001t0001g0032 a0001c0001t0001g0082 a0001c0001t0001g0083 others(3): Show |
7 | HG04184.hp1 NA18946.hp1 NA18965.hp1 others(4): Show |
intron_variant | MODIFIER | c.562-611C>T | MFNG | ENSG00000100060.18 | transcript | ENST00000356998.8 | protein_coding | 4/7 | chr22 | 37477592 | |||||||
| chr22:37477896 | C | T | 1 | a0001c0001t0001g0035 | 2 | HG01257.hp2 HG01258.hp2 |
intron_variant | MODIFIER | c.562-915G>A | MFNG | ENSG00000100060.18 | transcript | ENST00000356998.8 | protein_coding | 4/7 | chr22 | 37477896 | |||||||
| chr22:37478028 | G | C | 36 | a0001c0001t0001g0006 a0001c0001t0001g0010 a0001c0001t0001g0011 others(33): Show |
56 | HG00639.hp2 HG00642.hp2 HG00735.hp2 others(53): Show |
intron_variant | MODIFIER | c.562-1047C>G | MFNG | ENSG00000100060.18 | transcript | ENST00000356998.8 | protein_coding | 4/7 | chr22 | 37478028 | |||||||
| chr22:37478078 | T | C | 1 | a0001c0001t0001g0048 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.562-1097A>G | MFNG | ENSG00000100060.18 | transcript | ENST00000356998.8 | protein_coding | 4/7 | chr22 | 37478078 | |||||||
| chr22:37478079 | C | T | 1 | a0001c0001t0001g0048 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.562-1098G>A | MFNG | ENSG00000100060.18 | transcript | ENST00000356998.8 | protein_coding | 4/7 | chr22 | 37478079 | |||||||
| chr22:37478223 | G | A | 1 | a0001c0001t0001g0113 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.561+1122C>T | MFNG | ENSG00000100060.18 | transcript | ENST00000356998.8 | protein_coding | 4/7 | chr22 | 37478223 | |||||||
| chr22:37478580 | T | G | 4 | a0001c0001t0001g0040 a0001c0001t0001g0064 a0001c0001t0001g0065 others(1): Show |
4 | HG02109.hp1 HG02572.hp1 HG02615.hp1 others(1): Show |
intron_variant | MODIFIER | c.561+765A>C | MFNG | ENSG00000100060.18 | transcript | ENST00000356998.8 | protein_coding | 4/7 | chr22 | 37478580 | |||||||
| chr22:37478620 | A | G | 1 | a0001c0001t0001g0096 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.561+725T>C | MFNG | ENSG00000100060.18 | transcript | ENST00000356998.8 | protein_coding | 4/7 | chr22 | 37478620 | |||||||
| chr22:37478673 | A | AT | 17 | a0001c0001t0001g0007 a0001c0001t0001g0019 a0001c0001t0001g0034 others(14): Show |
24 | HG00621.hp2 HG00741.hp2 HG01109.hp2 others(21): Show |
intron_variant | MODIFIER | c.561+671dupA | MFNG | ENSG00000100060.18 | transcript | ENST00000356998.8 | protein_coding | 4/7 | chr22 | 37478673 | |||||||
| chr22:37478673 | AT | A | 7 | a0001c0001t0001g0010 a0001c0001t0001g0067 a0001c0001t0001g0105 others(4): Show |
10 | HG00642.hp2 HG01167.hp1 HG01169.hp2 others(7): Show |
intron_variant | MODIFIER | c.561+671delA | MFNG | ENSG00000100060.18 | transcript | ENST00000356998.8 | protein_coding | 4/7 | chr22 | 37478673 | |||||||
| chr22:37478903 | T | C | 1 | a0001c0001t0001g0036 | 2 | HG01099.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.561+442A>G | MFNG | ENSG00000100060.18 | transcript | ENST00000356998.8 | protein_coding | 4/7 | chr22 | 37478903 | |||||||
| chr22:37478908 | A | C | 1 | a0001c0001t0001g0095 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.561+437T>G | MFNG | ENSG00000100060.18 | transcript | ENST00000356998.8 | protein_coding | 4/7 | chr22 | 37478908 | |||||||
| chr22:37478973 | C | G | 1 | a0001c0002t0001g0025 | 2 | HG03098.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.561+372G>C | MFNG | ENSG00000100060.18 | transcript | ENST00000356998.8 | protein_coding | 4/7 | chr22 | 37478973 | |||||||
| chr22:37479288 | C | T | 2 | a0001c0001t0001g0013 a0001c0001t0001g0047 |
4 | HG02258.hp2 HG02559.hp2 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.561+57G>A | MFNG | ENSG00000100060.18 | transcript | ENST00000356998.8 | protein_coding | 4/7 | chr22 | 37479288 | |||||||
| chr22:37479578 | A | G | 2 | a0001c0001t0001g0008 a0001c0001t0001g0126 |
6 | HG02886.hp2 HG03471.hp2 NA18522.hp2 others(3): Show |
intron_variant | MODIFIER | c.408-80T>C | MFNG | ENSG00000100060.18 | transcript | ENST00000356998.8 | protein_coding | 3/7 | chr22 | 37479578 | |||||||
| chr22:37479586 | G | A | 1 | a0001c0001t0001g0069 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.408-88C>T | MFNG | ENSG00000100060.18 | transcript | ENST00000356998.8 | protein_coding | 3/7 | chr22 | 37479586 | |||||||
| chr22:37479741 | C | T | 1 | a0001c0001t0001g0135 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.408-243G>A | MFNG | ENSG00000100060.18 | transcript | ENST00000356998.8 | protein_coding | 3/7 | chr22 | 37479741 | |||||||
| chr22:37479799 | T | C | 1 | a0001c0002t0001g0025 | 2 | HG03098.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.408-301A>G | MFNG | ENSG00000100060.18 | transcript | ENST00000356998.8 | protein_coding | 3/7 | chr22 | 37479799 | |||||||
| chr22:37479825 | G | T | 1 | a0001c0001t0001g0114 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.408-327C>A | MFNG | ENSG00000100060.18 | transcript | ENST00000356998.8 | protein_coding | 3/7 | chr22 | 37479825 | |||||||
| chr22:37479826 | A | G | 1 | a0001c0001t0001g0114 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.408-328T>C | MFNG | ENSG00000100060.18 | transcript | ENST00000356998.8 | protein_coding | 3/7 | chr22 | 37479826 | |||||||
| chr22:37479829 | C | A | 1 | a0001c0001t0001g0114 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.408-331G>T | MFNG | ENSG00000100060.18 | transcript | ENST00000356998.8 | protein_coding | 3/7 | chr22 | 37479829 | |||||||
| chr22:37479919 | G | A | 2 | a0001c0001t0001g0009 a0001c0001t0001g0024 |
6 | HG01175.hp2 HG01256.hp2 HG01258.hp1 others(3): Show |
intron_variant | MODIFIER | c.407+278C>T | MFNG | ENSG00000100060.18 | transcript | ENST00000356998.8 | protein_coding | 3/7 | chr22 | 37479919 | |||||||
| chr22:37479929 | A | G | 2 | a0001c0002t0001g0025 a0001c0002t0001g0044 |
3 | HG03098.hp2 HG03453.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.407+268T>C | MFNG | ENSG00000100060.18 | transcript | ENST00000356998.8 | protein_coding | 3/7 | chr22 | 37479929 | |||||||
| chr22:37480482 | C | G | 1 | a0001c0001t0001g0134 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.305-183G>C | MFNG | ENSG00000100060.18 | transcript | ENST00000356998.8 | protein_coding | 2/7 | chr22 | 37480482 | |||||||
| chr22:37480488 | G | C | 16 | a0001c0001t0001g0016 a0001c0001t0001g0028 a0001c0001t0001g0029 others(13): Show |
21 | HG00735.hp2 HG00741.hp1 HG01099.hp2 others(18): Show |
intron_variant | MODIFIER | c.305-189C>G | MFNG | ENSG00000100060.18 | transcript | ENST00000356998.8 | protein_coding | 2/7 | chr22 | 37480488 | |||||||
| chr22:37480702 | C | T | 1 | a0005c0004t0001g0080 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.304+19G>A | MFNG | ENSG00000100060.18 | transcript | ENST00000356998.8 | protein_coding | 2/7 | chr22 | 37480702 | |||||||
| chr22:37481091 | A | T | 1 | a0001c0007t0001g0046 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.256-322T>A | MFNG | ENSG00000100060.18 | transcript | ENST00000356998.8 | protein_coding | 1/7 | chr22 | 37481091 | |||||||
| chr22:37481139 | G | A | 6 | a0001c0001t0001g0012 a0001c0001t0001g0037 a0001c0001t0001g0130 others(3): Show |
10 | HG00438.hp1 HG00558.hp2 HG01928.hp2 others(7): Show |
intron_variant | MODIFIER | c.256-370C>T | MFNG | ENSG00000100060.18 | transcript | ENST00000356998.8 | protein_coding | 1/7 | chr22 | 37481139 | |||||||
| chr22:37481226 | A | G | 1 | a0001c0001t0001g0133 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.256-457T>C | MFNG | ENSG00000100060.18 | transcript | ENST00000356998.8 | protein_coding | 1/7 | chr22 | 37481226 | |||||||
| chr22:37481358 | G | A | 2 | a0001c0001t0001g0008 a0001c0001t0001g0126 |
6 | HG02886.hp2 HG03471.hp2 NA18522.hp2 others(3): Show |
intron_variant | MODIFIER | c.256-589C>T | MFNG | ENSG00000100060.18 | transcript | ENST00000356998.8 | protein_coding | 1/7 | chr22 | 37481358 | |||||||
| chr22:37481404 | T | G | 1 | a0001c0001t0001g0088 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.256-635A>C | MFNG | ENSG00000100060.18 | transcript | ENST00000356998.8 | protein_coding | 1/7 | chr22 | 37481404 | |||||||
| chr22:37481414 | T | C | 1 | a0001c0001t0001g0030 | 2 | HG02258.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.256-645A>G | MFNG | ENSG00000100060.18 | transcript | ENST00000356998.8 | protein_coding | 1/7 | chr22 | 37481414 | |||||||
| chr22:37481670 | C | A | 1 | a0001c0001t0001g0070 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.256-901G>T | MFNG | ENSG00000100060.18 | transcript | ENST00000356998.8 | protein_coding | 1/7 | chr22 | 37481670 | |||||||
| chr22:37481687 | C | G | 1 | a0001c0001t0001g0132 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.256-918G>C | MFNG | ENSG00000100060.18 | transcript | ENST00000356998.8 | protein_coding | 1/7 | chr22 | 37481687 | |||||||
| chr22:37481830 | C | T | 1 | a0001c0001t0001g0045 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.256-1061G>A | MFNG | ENSG00000100060.18 | transcript | ENST00000356998.8 | protein_coding | 1/7 | chr22 | 37481830 | |||||||
| chr22:37481923 | G | C | 3 | a0001c0001t0001g0071 a0001c0001t0001g0072 a0001c0002t0001g0044 |
3 | HG02896.hp1 HG02897.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.256-1154C>G | MFNG | ENSG00000100060.18 | transcript | ENST00000356998.8 | protein_coding | 1/7 | chr22 | 37481923 | |||||||
| chr22:37481971 | T | C | 1 | a0001c0001t0001g0027 | 2 | HG00639.hp1 HG02451.hp1 |
intron_variant | MODIFIER | c.256-1202A>G | MFNG | ENSG00000100060.18 | transcript | ENST00000356998.8 | protein_coding | 1/7 | chr22 | 37481971 | |||||||
| chr22:37482394 | T | C | 6 | a0001c0001t0001g0032 a0001c0001t0001g0082 a0001c0001t0001g0083 others(3): Show |
7 | HG04184.hp1 NA18946.hp1 NA18965.hp1 others(4): Show |
intron_variant | MODIFIER | c.256-1625A>G | MFNG | ENSG00000100060.18 | transcript | ENST00000356998.8 | protein_coding | 1/7 | chr22 | 37482394 | |||||||
| chr22:37482396 | C | T | 1 | a0001c0001t0001g0110 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.256-1627G>A | MFNG | ENSG00000100060.18 | transcript | ENST00000356998.8 | protein_coding | 1/7 | chr22 | 37482396 | |||||||
| chr22:37482429 | TCACACAC others(3): Show |
T | 17 | a0001c0001t0001g0016 a0001c0001t0001g0028 a0001c0001t0001g0029 others(14): Show |
22 | HG00735.hp2 HG00741.hp1 HG01099.hp2 others(19): Show |
intron_variant | MODIFIER | c.256-1670_256-1661d others(12): Show |
MFNG | ENSG00000100060.18 | transcript | ENST00000356998.8 | protein_coding | 1/7 | chr22 | 37482429 | |||||||
| chr22:37482453 | G | A | 2 | a0001c0001t0001g0038 a0001c0001t0001g0143 |
3 | NA18945.hp2 NA18952.hp1 NA19060.hp2 |
intron_variant | MODIFIER | c.256-1684C>T | MFNG | ENSG00000100060.18 | transcript | ENST00000356998.8 | protein_coding | 1/7 | chr22 | 37482453 | |||||||
| chr22:37482460 | T | TAC | 23 | a0001c0001t0001g0002 a0001c0001t0001g0008 a0001c0001t0001g0012 others(20): Show |
55 | HG00323.hp2 HG00438.hp1 HG00544.hp1 others(52): Show |
intron_variant | MODIFIER | c.256-1693_256-1692d others(4): Show |
MFNG | ENSG00000100060.18 | transcript | ENST00000356998.8 | protein_coding | 1/7 | chr22 | 37482460 | |||||||
| chr22:37482460 | T | TACAC | 3 | a0001c0001t0001g0038 a0001c0001t0001g0141 a0001c0001t0001g0143 |
4 | NA18945.hp2 NA18952.hp1 NA19060.hp2 others(1): Show |
intron_variant | MODIFIER | c.256-1695_256-1692d others(6): Show |
MFNG | ENSG00000100060.18 | transcript | ENST00000356998.8 | protein_coding | 1/7 | chr22 | 37482460 | |||||||
| chr22:37482460 | TAC | T | 3 | a0001c0001t0001g0043 a0001c0001t0001g0093 a0001c0001t0001g0094 |
3 | HG02257.hp1 HG03490.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.256-1693_256-1692d others(4): Show |
MFNG | ENSG00000100060.18 | transcript | ENST00000356998.8 | protein_coding | 1/7 | chr22 | 37482460 | |||||||
| chr22:37482489 | G | A | 1 | a0001c0001t0001g0119 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.256-1720C>T | MFNG | ENSG00000100060.18 | transcript | ENST00000356998.8 | protein_coding | 1/7 | chr22 | 37482489 | |||||||
| chr22:37482493 | G | A | 1 | a0001c0001t0001g0073 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.256-1724C>T | MFNG | ENSG00000100060.18 | transcript | ENST00000356998.8 | protein_coding | 1/7 | chr22 | 37482493 | |||||||
| chr22:37482559 | T | C | 2 | a0001c0001t0001g0043 a0001c0002t0001g0044 |
2 | HG03453.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.256-1790A>G | MFNG | ENSG00000100060.18 | transcript | ENST00000356998.8 | protein_coding | 1/7 | chr22 | 37482559 | |||||||
| chr22:37482813 | T | C | 2 | a0001c0001t0001g0043 a0001c0002t0001g0044 |
2 | HG03453.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.256-2044A>G | MFNG | ENSG00000100060.18 | transcript | ENST00000356998.8 | protein_coding | 1/7 | chr22 | 37482813 | |||||||
| chr22:37483179 | C | T | 2 | a0001c0001t0001g0089 a0001c0001t0001g0091 |
2 | HG00741.hp2 HG01167.hp2 |
intron_variant | MODIFIER | c.256-2410G>A | MFNG | ENSG00000100060.18 | transcript | ENST00000356998.8 | protein_coding | 1/7 | chr22 | 37483179 | |||||||
| chr22:37483186 | G | A | 2 | a0001c0001t0001g0043 a0001c0002t0001g0044 |
2 | HG03453.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.256-2417C>T | MFNG | ENSG00000100060.18 | transcript | ENST00000356998.8 | protein_coding | 1/7 | chr22 | 37483186 | |||||||
| chr22:37483241 | G | A | 3 | a0001c0001t0001g0029 a0001c0001t0001g0111 a0001c0001t0001g0115 |
4 | HG00735.hp2 HG00741.hp1 HG01192.hp1 others(1): Show |
intron_variant | MODIFIER | c.256-2472C>T | MFNG | ENSG00000100060.18 | transcript | ENST00000356998.8 | protein_coding | 1/7 | chr22 | 37483241 | |||||||
| chr22:37483344 | G | A | 2 | a0001c0001t0001g0042 a0001c0001t0001g0125 |
2 | HG01109.hp1 HG02155.hp2 |
intron_variant | MODIFIER | c.256-2575C>T | MFNG | ENSG00000100060.18 | transcript | ENST00000356998.8 | protein_coding | 1/7 | chr22 | 37483344 | |||||||
| chr22:37483389 | T | C | 1 | a0001c0001t0001g0142 | 1 | NA18957.hp2 | intron_variant | MODIFIER | c.255+2534A>G | MFNG | ENSG00000100060.18 | transcript | ENST00000356998.8 | protein_coding | 1/7 | chr22 | 37483389 | |||||||
| chr22:37483418 | C | G | 1 | a0001c0001t0001g0142 | 1 | NA18957.hp2 | intron_variant | MODIFIER | c.255+2505G>C | MFNG | ENSG00000100060.18 | transcript | ENST00000356998.8 | protein_coding | 1/7 | chr22 | 37483418 | |||||||
| chr22:37483434 | C | A | 25 | a0001c0001t0001g0002 a0001c0001t0001g0012 a0001c0001t0001g0017 others(22): Show |
54 | HG00323.hp2 HG00438.hp1 HG00544.hp1 others(51): Show |
intron_variant | MODIFIER | c.255+2489G>T | MFNG | ENSG00000100060.18 | transcript | ENST00000356998.8 | protein_coding | 1/7 | chr22 | 37483434 | |||||||
| chr22:37483520 | G | A | 23 | a0001c0001t0001g0002 a0001c0001t0001g0012 a0001c0001t0001g0017 others(20): Show |
52 | HG00323.hp2 HG00438.hp1 HG00544.hp1 others(49): Show |
intron_variant | MODIFIER | c.255+2403C>T | MFNG | ENSG00000100060.18 | transcript | ENST00000356998.8 | protein_coding | 1/7 | chr22 | 37483520 | |||||||
| chr22:37483552 | A | G | 3 | a0001c0001t0001g0043 a0001c0002t0001g0025 a0001c0002t0001g0044 |
4 | HG03098.hp2 HG03453.hp2 HG03516.hp1 others(1): Show |
intron_variant | MODIFIER | c.255+2371T>C | MFNG | ENSG00000100060.18 | transcript | ENST00000356998.8 | protein_coding | 1/7 | chr22 | 37483552 | |||||||
| chr22:37483705 | G | A | 1 | a0001c0001t0001g0074 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.255+2218C>T | MFNG | ENSG00000100060.18 | transcript | ENST00000356998.8 | protein_coding | 1/7 | chr22 | 37483705 | |||||||
| chr22:37483834 | G | A | 2 | a0001c0001t0001g0008 a0001c0001t0001g0126 |
6 | HG02886.hp2 HG03471.hp2 NA18522.hp2 others(3): Show |
intron_variant | MODIFIER | c.255+2089C>T | MFNG | ENSG00000100060.18 | transcript | ENST00000356998.8 | protein_coding | 1/7 | chr22 | 37483834 | |||||||
| chr22:37483849 | G | C | 1 | a0001c0001t0001g0002 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.255+2074C>G | MFNG | ENSG00000100060.18 | transcript | ENST00000356998.8 | protein_coding | 1/7 | chr22 | 37483849 | |||||||
| chr22:37484012 | G | A | 2 | a0001c0001t0001g0001 a0001c0001t0001g0042 |
2 | HG02155.hp2 NA18948.hp2 |
intron_variant | MODIFIER | c.255+1911C>T | MFNG | ENSG00000100060.18 | transcript | ENST00000356998.8 | protein_coding | 1/7 | chr22 | 37484012 | |||||||
| chr22:37484135 | G | A | 2 | a0001c0001t0001g0043 a0001c0002t0001g0044 |
2 | HG03453.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.255+1788C>T | MFNG | ENSG00000100060.18 | transcript | ENST00000356998.8 | protein_coding | 1/7 | chr22 | 37484135 | |||||||
| chr22:37484235 | C | T | 1 | a0001c0001t0001g0092 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.255+1688G>A | MFNG | ENSG00000100060.18 | transcript | ENST00000356998.8 | protein_coding | 1/7 | chr22 | 37484235 | |||||||
| chr22:37484406 | T | G | 1 | a0001c0001t0001g0142 | 1 | NA18957.hp2 | intron_variant | MODIFIER | c.255+1517A>C | MFNG | ENSG00000100060.18 | transcript | ENST00000356998.8 | protein_coding | 1/7 | chr22 | 37484406 | |||||||
| chr22:37484416 | A | AGCGAGGG others(393): Show |
1 | a0001c0001t0001g0143 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.255+1506_255+1507i others(402): Show |
MFNG | ENSG00000100060.18 | transcript | ENST00000356998.8 | protein_coding | 1/7 | chr22 | 37484416 | |||||||
| chr22:37484416 | A | AGCGAGGG others(392): Show |
21 | a0001c0001t0001g0002 a0001c0001t0001g0012 a0001c0001t0001g0017 others(18): Show |
50 | HG00323.hp2 HG00438.hp1 HG00544.hp1 others(47): Show |
intron_variant | MODIFIER | c.255+1506_255+1507i others(401): Show |
MFNG | ENSG00000100060.18 | transcript | ENST00000356998.8 | protein_coding | 1/7 | chr22 | 37484416 | |||||||
| chr22:37484416 | A | AGCGAGGG others(391): Show |
1 | a0001c0001t0001g0142 | 1 | NA18957.hp2 | intron_variant | MODIFIER | c.255+1506_255+1507i others(400): Show |
MFNG | ENSG00000100060.18 | transcript | ENST00000356998.8 | protein_coding | 1/7 | chr22 | 37484416 | |||||||
| chr22:37484550 | G | A | 1 | a0001c0001t0001g0081 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.255+1373C>T | MFNG | ENSG00000100060.18 | transcript | ENST00000356998.8 | protein_coding | 1/7 | chr22 | 37484550 | |||||||
| chr22:37484572 | C | T | 1 | a0001c0001t0001g0112 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.255+1351G>A | MFNG | ENSG00000100060.18 | transcript | ENST00000356998.8 | protein_coding | 1/7 | chr22 | 37484572 | |||||||
| chr22:37484630 | G | C | 23 | a0001c0001t0001g0002 a0001c0001t0001g0012 a0001c0001t0001g0017 others(20): Show |
52 | HG00323.hp2 HG00438.hp1 HG00544.hp1 others(49): Show |
intron_variant | MODIFIER | c.255+1293C>G | MFNG | ENSG00000100060.18 | transcript | ENST00000356998.8 | protein_coding | 1/7 | chr22 | 37484630 | |||||||
| chr22:37484635 | G | A | 1 | a0001c0001t0001g0091 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.255+1288C>T | MFNG | ENSG00000100060.18 | transcript | ENST00000356998.8 | protein_coding | 1/7 | chr22 | 37484635 | |||||||
| chr22:37484691 | C | T | 4 | a0001c0001t0001g0026 a0001c0001t0001g0089 a0001c0001t0001g0090 others(1): Show |
5 | HG00741.hp2 HG01069.hp1 HG01167.hp2 others(2): Show |
intron_variant | MODIFIER | c.255+1232G>A | MFNG | ENSG00000100060.18 | transcript | ENST00000356998.8 | protein_coding | 1/7 | chr22 | 37484691 | |||||||
| chr22:37484702 | G | T | 1 | a0001c0001t0001g0088 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.255+1221C>A | MFNG | ENSG00000100060.18 | transcript | ENST00000356998.8 | protein_coding | 1/7 | chr22 | 37484702 | |||||||
| chr22:37484753 | G | A | 1 | a0001c0001t0001g0075 | 1 | NA18993.hp2 | intron_variant | MODIFIER | c.255+1170C>T | MFNG | ENSG00000100060.18 | transcript | ENST00000356998.8 | protein_coding | 1/7 | chr22 | 37484753 | |||||||
| chr22:37484834 | C | G | 2 | a0001c0001t0001g0078 a0001c0001t0001g0079 |
2 | HG00408.hp1 HG02080.hp1 |
intron_variant | MODIFIER | c.255+1089G>C | MFNG | ENSG00000100060.18 | transcript | ENST00000356998.8 | protein_coding | 1/7 | chr22 | 37484834 | |||||||
| chr22:37484840 | G | A | 1 | a0004c0005t0001g0076 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.255+1083C>T | MFNG | ENSG00000100060.18 | transcript | ENST00000356998.8 | protein_coding | 1/7 | chr22 | 37484840 | |||||||
| chr22:37484971 | A | ATG | 32 | a0001c0001t0001g0006 a0001c0001t0001g0011 a0001c0001t0001g0016 others(29): Show |
47 | HG00735.hp2 HG00741.hp1 HG01099.hp2 others(44): Show |
intron_variant | MODIFIER | c.255+950_255+951dup others(2): Show |
MFNG | ENSG00000100060.18 | transcript | ENST00000356998.8 | protein_coding | 1/7 | chr22 | 37484971 | |||||||
| chr22:37484971 | A | ATGTG | 7 | a0001c0001t0001g0030 a0001c0001t0001g0081 a0001c0001t0001g0107 others(4): Show |
8 | HG01515.hp2 HG02132.hp2 HG02258.hp1 others(5): Show |
intron_variant | MODIFIER | c.255+948_255+951dup others(4): Show |
MFNG | ENSG00000100060.18 | transcript | ENST00000356998.8 | protein_coding | 1/7 | chr22 | 37484971 | |||||||
| chr22:37484971 | ATG | A | 23 | a0001c0001t0001g0002 a0001c0001t0001g0012 a0001c0001t0001g0017 others(20): Show |
52 | HG00323.hp2 HG00438.hp1 HG00544.hp1 others(49): Show |
intron_variant | MODIFIER | c.255+950_255+951del others(2): Show |
MFNG | ENSG00000100060.18 | transcript | ENST00000356998.8 | protein_coding | 1/7 | chr22 | 37484971 | |||||||
| chr22:37485006 | C | T | 1 | a0001c0001t0001g0040 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.255+917G>A | MFNG | ENSG00000100060.18 | transcript | ENST00000356998.8 | protein_coding | 1/7 | chr22 | 37485006 | |||||||
| chr22:37485080 | G | A | 23 | a0001c0001t0001g0002 a0001c0001t0001g0012 a0001c0001t0001g0017 others(20): Show |
52 | HG00323.hp2 HG00438.hp1 HG00544.hp1 others(49): Show |
intron_variant | MODIFIER | c.255+843C>T | MFNG | ENSG00000100060.18 | transcript | ENST00000356998.8 | protein_coding | 1/7 | chr22 | 37485080 | |||||||
| chr22:37485081 | G | A | 1 | a0001c0001t0001g0030 | 2 | HG02258.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.255+842C>T | MFNG | ENSG00000100060.18 | transcript | ENST00000356998.8 | protein_coding | 1/7 | chr22 | 37485081 | |||||||
| chr22:37485147 | A | G | 1 | a0001c0001t0001g0030 | 2 | HG02258.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.255+776T>C | MFNG | ENSG00000100060.18 | transcript | ENST00000356998.8 | protein_coding | 1/7 | chr22 | 37485147 | |||||||
| chr22:37485173 | G | A | 12 | a0001c0001t0001g0016 a0001c0001t0001g0028 a0001c0001t0001g0029 others(9): Show |
16 | HG00735.hp2 HG00741.hp1 HG01099.hp2 others(13): Show |
intron_variant | MODIFIER | c.255+750C>T | MFNG | ENSG00000100060.18 | transcript | ENST00000356998.8 | protein_coding | 1/7 | chr22 | 37485173 | |||||||
| chr22:37485177 | G | A | 11 | a0001c0001t0001g0006 a0001c0001t0001g0011 a0001c0001t0001g0033 others(8): Show |
20 | HG01109.hp1 HG01243.hp2 HG02622.hp2 others(17): Show |
intron_variant | MODIFIER | c.255+746C>T | MFNG | ENSG00000100060.18 | transcript | ENST00000356998.8 | protein_coding | 1/7 | chr22 | 37485177 | |||||||
| chr22:37485183 | G | GCA | 2 | a0001c0001t0001g0030 a0001c0001t0001g0121 |
3 | HG02055.hp1 HG02258.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.255+738_255+739dup others(2): Show |
MFNG | ENSG00000100060.18 | transcript | ENST00000356998.8 | protein_coding | 1/7 | chr22 | 37485183 | |||||||
| chr22:37485183 | G | GCACA | 22 | a0001c0001t0001g0002 a0001c0001t0001g0012 a0001c0001t0001g0017 others(19): Show |
51 | HG00323.hp2 HG00438.hp1 HG00544.hp1 others(48): Show |
intron_variant | MODIFIER | c.255+736_255+739dup others(4): Show |
MFNG | ENSG00000100060.18 | transcript | ENST00000356998.8 | protein_coding | 1/7 | chr22 | 37485183 | |||||||
| chr22:37485259 | G | A | 1 | a0001c0001t0001g0031 | 2 | NA18982.hp1 NA18997.hp2 |
intron_variant | MODIFIER | c.255+664C>T | MFNG | ENSG00000100060.18 | transcript | ENST00000356998.8 | protein_coding | 1/7 | chr22 | 37485259 | |||||||
| chr22:37485356 | G | A | 2 | a0001c0001t0001g0078 a0001c0001t0001g0079 |
2 | HG00408.hp1 HG02080.hp1 |
intron_variant | MODIFIER | c.255+567C>T | MFNG | ENSG00000100060.18 | transcript | ENST00000356998.8 | protein_coding | 1/7 | chr22 | 37485356 | |||||||
| chr22:37485361 | A | G | 1 | a0001c0001t0001g0125 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.255+562T>C | MFNG | ENSG00000100060.18 | transcript | ENST00000356998.8 | protein_coding | 1/7 | chr22 | 37485361 | |||||||
| chr22:37485383 | T | C | 1 | a0005c0004t0001g0080 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.255+540A>G | MFNG | ENSG00000100060.18 | transcript | ENST00000356998.8 | protein_coding | 1/7 | chr22 | 37485383 | |||||||
| chr22:37485404 | C | T | 23 | a0001c0001t0001g0002 a0001c0001t0001g0012 a0001c0001t0001g0017 others(20): Show |
52 | HG00323.hp2 HG00438.hp1 HG00544.hp1 others(49): Show |
intron_variant | MODIFIER | c.255+519G>A | MFNG | ENSG00000100060.18 | transcript | ENST00000356998.8 | protein_coding | 1/7 | chr22 | 37485404 | |||||||
| chr22:37485475 | G | A | 3 | a0001c0001t0001g0032 a0001c0001t0001g0122 a0001c0001t0001g0123 |
4 | NA18946.hp1 NA18965.hp1 NA18986.hp1 others(1): Show |
intron_variant | MODIFIER | c.255+448C>T | MFNG | ENSG00000100060.18 | transcript | ENST00000356998.8 | protein_coding | 1/7 | chr22 | 37485475 | |||||||
| chr22:37485475 | G | C | 64 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0006 others(61): Show |
108 | HG00609.hp1 HG00621.hp1 HG00639.hp1 others(105): Show |
intron_variant | MODIFIER | c.255+448C>G | MFNG | ENSG00000100060.18 | transcript | ENST00000356998.8 | protein_coding | 1/7 | chr22 | 37485475 | |||||||
| chr22:37485596 | G | A | 1 | a0001c0001t0001g0124 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.255+327C>T | MFNG | ENSG00000100060.18 | transcript | ENST00000356998.8 | protein_coding | 1/7 | chr22 | 37485596 | |||||||
| chr22:37485687 | G | C | 8 | a0001c0001t0001g0006 a0001c0001t0001g0008 a0001c0001t0001g0011 others(5): Show |
21 | HG01109.hp1 HG02622.hp2 HG02717.hp1 others(18): Show |
intron_variant | MODIFIER | c.255+236C>G | MFNG | ENSG00000100060.18 | transcript | ENST00000356998.8 | protein_coding | 1/7 | chr22 | 37485687 | |||||||
| chr22:37485804 | G | A | 23 | a0001c0001t0001g0002 a0001c0001t0001g0012 a0001c0001t0001g0017 others(20): Show |
52 | HG00323.hp2 HG00438.hp1 HG00544.hp1 others(49): Show |
intron_variant | MODIFIER | c.255+119C>T | MFNG | ENSG00000100060.18 | transcript | ENST00000356998.8 | protein_coding | 1/7 | chr22 | 37485804 |