Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 8076 |
| ensemblid | ENSG00000197614.11 |
| hgncid | 29673 |
| symbol | MFAP5 |
| name | microfibril associated protein 5 |
| refseq_nuc | NM_003480.4 |
| refseq_prot | NP_003471.1 |
| ensembl_nuc | ENST00000359478.7 |
| ensembl_prot | ENSP00000352455.2 |
| mane_status | MANE Select |
| chr | chr12 |
| start | 8645943 |
| end | 8662826 |
| strand | - |
| ver | v1.2 |
| region | chr12:8645943-8662826 |
| region5000 | chr12:8640943-8667826 |
| regionname0 | MFAP5_chr12_8645943_8662826 |
| regionname5000 | MFAP5_chr12_8640943_8667826 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 173 | 371 | 92 | 70 | 149 | 12 | 46 | 108 | MFAP5_chr12_8640943_8667826 | MFAP5 | MSLLG others(168): Show |
chr12 | 8640943 | 8667826 |
| a0002 | 0/0 | 173 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | MFAP5_chr12_8640943_8667826 | MFAP5 | MSLLG others(168): Show |
chr12 | 8640943 | 8667826 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 519 | 370 | 91 | 70 | 149 | 12 | 46 | MFAP5_chr12_8640943_8667826 | MFAP5 | ATGTC others(514): Show |
chr12 | 8640943 | 8667826 | ||
| a0001c0003 | 0/0 | 519 | 1 | 1 | 0 | 0 | 0 | 0 | MFAP5_chr12_8640943_8667826 | MFAP5 | ATGTC others(514): Show |
chr12 | 8640943 | 8667826 | ||
| a0002c0002 | 0/0 | 519 | 1 | 0 | 0 | 1 | 0 | 0 | MFAP5_chr12_8640943_8667826 | MFAP5 | ATGTC others(514): Show |
chr12 | 8640943 | 8667826 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 1/0 | 2872 | 289 | 59 | 46 | 140 | 5 | 38 | MFAP5_chr12_8640943_8667826 | MFAP5 | ATTGT others(2867): Show |
chr12 | 8640943 | 8667826 |
| a0001c0001t0002 | 0/0 | 2872 | 19 | 4 | 10 | 0 | 3 | 2 | MFAP5_chr12_8640943_8667826 | MFAP5 | ATTGT others(2867): Show |
chr12 | 8640943 | 8667826 |
| a0001c0001t0003 | 0/0 | 2873 | 12 | 9 | 3 | 0 | 0 | 0 | MFAP5_chr12_8640943_8667826 | MFAP5 | ATTGT others(2868): Show |
chr12 | 8640943 | 8667826 |
| a0001c0001t0004 | 0/1 | 2872 | 11 | 1 | 4 | 0 | 3 | 2 | MFAP5_chr12_8640943_8667826 | MFAP5 | ATTGT others(2867): Show |
chr12 | 8640943 | 8667826 |
| a0001c0001t0005 | 0/0 | 2872 | 10 | 4 | 0 | 4 | 0 | 2 | MFAP5_chr12_8640943_8667826 | MFAP5 | ATTGT others(2867): Show |
chr12 | 8640943 | 8667826 |
| a0001c0001t0006 | 0/0 | 2872 | 6 | 6 | 0 | 0 | 0 | 0 | MFAP5_chr12_8640943_8667826 | MFAP5 | ATTGT others(2867): Show |
chr12 | 8640943 | 8667826 |
| a0001c0001t0007 | 0/0 | 2871 | 5 | 0 | 5 | 0 | 0 | 0 | MFAP5_chr12_8640943_8667826 | MFAP5 | ATTGT others(2866): Show |
chr12 | 8640943 | 8667826 |
| a0001c0001t0008 | 0/0 | 2872 | 4 | 2 | 2 | 0 | 0 | 0 | MFAP5_chr12_8640943_8667826 | MFAP5 | ATTGT others(2867): Show |
chr12 | 8640943 | 8667826 |
| a0001c0001t0009 | 0/0 | 2873 | 3 | 0 | 0 | 2 | 0 | 1 | MFAP5_chr12_8640943_8667826 | MFAP5 | ATTGT others(2868): Show |
chr12 | 8640943 | 8667826 |
| a0001c0001t0010 | 0/0 | 2872 | 2 | 2 | 0 | 0 | 0 | 0 | MFAP5_chr12_8640943_8667826 | MFAP5 | ATTGT others(2867): Show |
chr12 | 8640943 | 8667826 |
| a0001c0001t0011 | 0/0 | 2872 | 2 | 2 | 0 | 0 | 0 | 0 | MFAP5_chr12_8640943_8667826 | MFAP5 | ATTGT others(2867): Show |
chr12 | 8640943 | 8667826 |
| a0001c0001t0012 | 0/0 | 2873 | 1 | 1 | 0 | 0 | 0 | 0 | MFAP5_chr12_8640943_8667826 | MFAP5 | ATTGT others(2868): Show |
chr12 | 8640943 | 8667826 |
| a0001c0001t0013 | 0/0 | 2872 | 1 | 0 | 0 | 1 | 0 | 0 | MFAP5_chr12_8640943_8667826 | MFAP5 | ATTGT others(2867): Show |
chr12 | 8640943 | 8667826 |
| a0001c0001t0014 | 0/0 | 2872 | 1 | 0 | 0 | 1 | 0 | 0 | MFAP5_chr12_8640943_8667826 | MFAP5 | ATTGT others(2867): Show |
chr12 | 8640943 | 8667826 |
| a0001c0001t0015 | 0/0 | 2873 | 1 | 0 | 0 | 1 | 0 | 0 | MFAP5_chr12_8640943_8667826 | MFAP5 | ATTGT others(2868): Show |
chr12 | 8640943 | 8667826 |
| a0001c0001t0016 | 0/0 | 2872 | 1 | 0 | 0 | 0 | 1 | 0 | MFAP5_chr12_8640943_8667826 | MFAP5 | ATTGT others(2867): Show |
chr12 | 8640943 | 8667826 |
| a0001c0001t0017 | 0/0 | 2873 | 1 | 1 | 0 | 0 | 0 | 0 | MFAP5_chr12_8640943_8667826 | MFAP5 | ATTGT others(2868): Show |
chr12 | 8640943 | 8667826 |
| a0001c0001t0018 | 0/0 | 2872 | 1 | 0 | 0 | 0 | 0 | 1 | MFAP5_chr12_8640943_8667826 | MFAP5 | ATTGT others(2867): Show |
chr12 | 8640943 | 8667826 |
| a0001c0003t0012 | 0/0 | 2873 | 1 | 1 | 0 | 0 | 0 | 0 | MFAP5_chr12_8640943_8667826 | MFAP5 | ATTGT others(2868): Show |
chr12 | 8640943 | 8667826 |
| a0002c0002t0001 | 0/0 | 2872 | 1 | 0 | 0 | 1 | 0 | 0 | MFAP5_chr12_8640943_8667826 | MFAP5 | ATTGT others(2867): Show |
chr12 | 8640943 | 8667826 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 0/0 | 37 | 3 | 9 | 20 | 2 | 3 | MFAP5_chr12_8640943_8667826 | MFAP5 | chr12 | 8640943 | 8667826 |
| a0001c0001t0001g0002 | 0/0 | 13 | 2 | 3 | 6 | 1 | 1 | MFAP5_chr12_8640943_8667826 | MFAP5 | chr12 | 8640943 | 8667826 |
| a0001c0001t0001g0004 | 0/0 | 7 | 0 | 5 | 2 | 0 | 0 | MFAP5_chr12_8640943_8667826 | MFAP5 | chr12 | 8640943 | 8667826 |
| a0001c0001t0001g0005 | 0/0 | 7 | 0 | 0 | 6 | 0 | 1 | MFAP5_chr12_8640943_8667826 | MFAP5 | chr12 | 8640943 | 8667826 |
| a0001c0001t0001g0006 | 0/0 | 7 | 0 | 0 | 7 | 0 | 0 | MFAP5_chr12_8640943_8667826 | MFAP5 | chr12 | 8640943 | 8667826 |
| a0001c0001t0001g0007 | 1/0 | 5 | 4 | 0 | 0 | 0 | 0 | MFAP5_chr12_8640943_8667826 | MFAP5 | chr12 | 8640943 | 8667826 |
| a0001c0001t0001g0008 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | MFAP5_chr12_8640943_8667826 | MFAP5 | chr12 | 8640943 | 8667826 |
| a0001c0001t0001g0009 | 0/0 | 4 | 0 | 1 | 3 | 0 | 0 | MFAP5_chr12_8640943_8667826 | MFAP5 | chr12 | 8640943 | 8667826 |
| a0001c0001t0001g0011 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | MFAP5_chr12_8640943_8667826 | MFAP5 | chr12 | 8640943 | 8667826 |
| a0001c0001t0001g0012 | 0/0 | 4 | 3 | 1 | 0 | 0 | 0 | MFAP5_chr12_8640943_8667826 | MFAP5 | chr12 | 8640943 | 8667826 |
| a0001c0001t0001g0013 | 0/0 | 4 | 1 | 2 | 0 | 1 | 0 | MFAP5_chr12_8640943_8667826 | MFAP5 | chr12 | 8640943 | 8667826 |
| a0001c0001t0001g0015 | 0/0 | 4 | 2 | 0 | 2 | 0 | 0 | MFAP5_chr12_8640943_8667826 | MFAP5 | chr12 | 8640943 | 8667826 |
| a0001c0001t0001g0016 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | MFAP5_chr12_8640943_8667826 | MFAP5 | chr12 | 8640943 | 8667826 |
| a0001c0001t0001g0017 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | MFAP5_chr12_8640943_8667826 | MFAP5 | chr12 | 8640943 | 8667826 |
| a0001c0001t0001g0019 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | MFAP5_chr12_8640943_8667826 | MFAP5 | chr12 | 8640943 | 8667826 |
| a0001c0001t0001g0020 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | MFAP5_chr12_8640943_8667826 | MFAP5 | chr12 | 8640943 | 8667826 |
| a0001c0001t0001g0021 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | MFAP5_chr12_8640943_8667826 | MFAP5 | chr12 | 8640943 | 8667826 |
| a0001c0001t0001g0022 | 0/0 | 3 | 1 | 1 | 0 | 1 | 0 | MFAP5_chr12_8640943_8667826 | MFAP5 | chr12 | 8640943 | 8667826 |
| a0001c0001t0001g0023 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | MFAP5_chr12_8640943_8667826 | MFAP5 | chr12 | 8640943 | 8667826 |
| a0001c0001t0001g0024 | 0/0 | 3 | 0 | 0 | 1 | 0 | 2 | MFAP5_chr12_8640943_8667826 | MFAP5 | chr12 | 8640943 | 8667826 |
| a0001c0001t0001g0025 | 0/0 | 3 | 0 | 1 | 2 | 0 | 0 | MFAP5_chr12_8640943_8667826 | MFAP5 | chr12 | 8640943 | 8667826 |
| a0001c0001t0001g0026 | 0/0 | 3 | 0 | 1 | 2 | 0 | 0 | MFAP5_chr12_8640943_8667826 | MFAP5 | chr12 | 8640943 | 8667826 |
| a0001c0001t0001g0027 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | MFAP5_chr12_8640943_8667826 | MFAP5 | chr12 | 8640943 | 8667826 |
| a0001c0001t0001g0028 | 0/0 | 3 | 2 | 1 | 0 | 0 | 0 | MFAP5_chr12_8640943_8667826 | MFAP5 | chr12 | 8640943 | 8667826 |
| a0001c0001t0001g0029 | 0/0 | 3 | 0 | 1 | 2 | 0 | 0 | MFAP5_chr12_8640943_8667826 | MFAP5 | chr12 | 8640943 | 8667826 |
| a0001c0001t0001g0030 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | MFAP5_chr12_8640943_8667826 | MFAP5 | chr12 | 8640943 | 8667826 |
| a0001c0001t0001g0031 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | MFAP5_chr12_8640943_8667826 | MFAP5 | chr12 | 8640943 | 8667826 |
| a0001c0001t0001g0035 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | MFAP5_chr12_8640943_8667826 | MFAP5 | chr12 | 8640943 | 8667826 |
| a0001c0001t0001g0036 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MFAP5_chr12_8640943_8667826 | MFAP5 | chr12 | 8640943 | 8667826 |
| a0001c0001t0001g0037 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MFAP5_chr12_8640943_8667826 | MFAP5 | chr12 | 8640943 | 8667826 |
| a0001c0001t0001g0038 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | MFAP5_chr12_8640943_8667826 | MFAP5 | chr12 | 8640943 | 8667826 |
| a0001c0001t0001g0039 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | MFAP5_chr12_8640943_8667826 | MFAP5 | chr12 | 8640943 | 8667826 |
| a0001c0001t0001g0040 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MFAP5_chr12_8640943_8667826 | MFAP5 | chr12 | 8640943 | 8667826 |
| a0001c0001t0001g0041 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MFAP5_chr12_8640943_8667826 | MFAP5 | chr12 | 8640943 | 8667826 |
| a0001c0001t0001g0044 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | MFAP5_chr12_8640943_8667826 | MFAP5 | chr12 | 8640943 | 8667826 |
| a0001c0001t0001g0045 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MFAP5_chr12_8640943_8667826 | MFAP5 | chr12 | 8640943 | 8667826 |
| a0001c0001t0001g0046 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | MFAP5_chr12_8640943_8667826 | MFAP5 | chr12 | 8640943 | 8667826 |
| a0001c0001t0001g0047 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | MFAP5_chr12_8640943_8667826 | MFAP5 | chr12 | 8640943 | 8667826 |
| a0001c0001t0001g0048 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MFAP5_chr12_8640943_8667826 | MFAP5 | chr12 | 8640943 | 8667826 |
| a0001c0001t0001g0049 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MFAP5_chr12_8640943_8667826 | MFAP5 | chr12 | 8640943 | 8667826 |
| a0001c0001t0001g0052 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | MFAP5_chr12_8640943_8667826 | MFAP5 | chr12 | 8640943 | 8667826 |
| a0001c0001t0001g0054 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MFAP5_chr12_8640943_8667826 | MFAP5 | chr12 | 8640943 | 8667826 |
| a0001c0001t0001g0055 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MFAP5_chr12_8640943_8667826 | MFAP5 | chr12 | 8640943 | 8667826 |
| a0001c0001t0001g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFAP5_chr12_8640943_8667826 | MFAP5 | chr12 | 8640943 | 8667826 |
| a0001c0001t0001g0072 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MFAP5_chr12_8640943_8667826 | MFAP5 | chr12 | 8640943 | 8667826 |
| a0001c0001t0001g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MFAP5_chr12_8640943_8667826 | MFAP5 | chr12 | 8640943 | 8667826 |
| a0001c0001t0001g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFAP5_chr12_8640943_8667826 | MFAP5 | chr12 | 8640943 | 8667826 |
| a0001c0001t0001g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFAP5_chr12_8640943_8667826 | MFAP5 | chr12 | 8640943 | 8667826 |
| a0001c0001t0001g0076 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MFAP5_chr12_8640943_8667826 | MFAP5 | chr12 | 8640943 | 8667826 |
| a0001c0001t0001g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFAP5_chr12_8640943_8667826 | MFAP5 | chr12 | 8640943 | 8667826 |
| a0001c0001t0001g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFAP5_chr12_8640943_8667826 | MFAP5 | chr12 | 8640943 | 8667826 |
| a0001c0001t0001g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFAP5_chr12_8640943_8667826 | MFAP5 | chr12 | 8640943 | 8667826 |
| a0001c0001t0001g0080 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MFAP5_chr12_8640943_8667826 | MFAP5 | chr12 | 8640943 | 8667826 |
| a0001c0001t0001g0081 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MFAP5_chr12_8640943_8667826 | MFAP5 | chr12 | 8640943 | 8667826 |
| a0001c0001t0001g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFAP5_chr12_8640943_8667826 | MFAP5 | chr12 | 8640943 | 8667826 |
| a0001c0001t0001g0083 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MFAP5_chr12_8640943_8667826 | MFAP5 | chr12 | 8640943 | 8667826 |
| a0001c0001t0001g0085 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MFAP5_chr12_8640943_8667826 | MFAP5 | chr12 | 8640943 | 8667826 |
| a0001c0001t0001g0086 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MFAP5_chr12_8640943_8667826 | MFAP5 | chr12 | 8640943 | 8667826 |
| a0001c0001t0001g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFAP5_chr12_8640943_8667826 | MFAP5 | chr12 | 8640943 | 8667826 |
| a0001c0001t0001g0088 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MFAP5_chr12_8640943_8667826 | MFAP5 | chr12 | 8640943 | 8667826 |
| a0001c0001t0001g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFAP5_chr12_8640943_8667826 | MFAP5 | chr12 | 8640943 | 8667826 |
| a0001c0001t0001g0090 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MFAP5_chr12_8640943_8667826 | MFAP5 | chr12 | 8640943 | 8667826 |
| a0001c0001t0001g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFAP5_chr12_8640943_8667826 | MFAP5 | chr12 | 8640943 | 8667826 |
| a0001c0001t0001g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFAP5_chr12_8640943_8667826 | MFAP5 | chr12 | 8640943 | 8667826 |
| a0001c0001t0001g0093 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MFAP5_chr12_8640943_8667826 | MFAP5 | chr12 | 8640943 | 8667826 |
| a0001c0001t0001g0094 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MFAP5_chr12_8640943_8667826 | MFAP5 | chr12 | 8640943 | 8667826 |
| a0001c0001t0001g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFAP5_chr12_8640943_8667826 | MFAP5 | chr12 | 8640943 | 8667826 |
| a0001c0001t0001g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFAP5_chr12_8640943_8667826 | MFAP5 | chr12 | 8640943 | 8667826 |
| a0001c0001t0001g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFAP5_chr12_8640943_8667826 | MFAP5 | chr12 | 8640943 | 8667826 |
| a0001c0001t0001g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFAP5_chr12_8640943_8667826 | MFAP5 | chr12 | 8640943 | 8667826 |
| a0001c0001t0001g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFAP5_chr12_8640943_8667826 | MFAP5 | chr12 | 8640943 | 8667826 |
| a0001c0001t0001g0101 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MFAP5_chr12_8640943_8667826 | MFAP5 | chr12 | 8640943 | 8667826 |
| a0001c0001t0001g0102 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MFAP5_chr12_8640943_8667826 | MFAP5 | chr12 | 8640943 | 8667826 |
| a0001c0001t0001g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFAP5_chr12_8640943_8667826 | MFAP5 | chr12 | 8640943 | 8667826 |
| a0001c0001t0001g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFAP5_chr12_8640943_8667826 | MFAP5 | chr12 | 8640943 | 8667826 |
| a0001c0001t0001g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFAP5_chr12_8640943_8667826 | MFAP5 | chr12 | 8640943 | 8667826 |
| a0001c0001t0001g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFAP5_chr12_8640943_8667826 | MFAP5 | chr12 | 8640943 | 8667826 |
| a0001c0001t0001g0109 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MFAP5_chr12_8640943_8667826 | MFAP5 | chr12 | 8640943 | 8667826 |
| a0001c0001t0001g0110 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MFAP5_chr12_8640943_8667826 | MFAP5 | chr12 | 8640943 | 8667826 |
| a0001c0001t0001g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFAP5_chr12_8640943_8667826 | MFAP5 | chr12 | 8640943 | 8667826 |
| a0001c0001t0001g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFAP5_chr12_8640943_8667826 | MFAP5 | chr12 | 8640943 | 8667826 |
| a0001c0001t0001g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFAP5_chr12_8640943_8667826 | MFAP5 | chr12 | 8640943 | 8667826 |
| a0001c0001t0001g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFAP5_chr12_8640943_8667826 | MFAP5 | chr12 | 8640943 | 8667826 |
| a0001c0001t0001g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFAP5_chr12_8640943_8667826 | MFAP5 | chr12 | 8640943 | 8667826 |
| a0001c0001t0001g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFAP5_chr12_8640943_8667826 | MFAP5 | chr12 | 8640943 | 8667826 |
| a0001c0001t0001g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFAP5_chr12_8640943_8667826 | MFAP5 | chr12 | 8640943 | 8667826 |
| a0001c0001t0001g0118 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MFAP5_chr12_8640943_8667826 | MFAP5 | chr12 | 8640943 | 8667826 |
| a0001c0001t0001g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFAP5_chr12_8640943_8667826 | MFAP5 | chr12 | 8640943 | 8667826 |
| a0001c0001t0001g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFAP5_chr12_8640943_8667826 | MFAP5 | chr12 | 8640943 | 8667826 |
| a0001c0001t0001g0122 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MFAP5_chr12_8640943_8667826 | MFAP5 | chr12 | 8640943 | 8667826 |
| a0001c0001t0001g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFAP5_chr12_8640943_8667826 | MFAP5 | chr12 | 8640943 | 8667826 |
| a0001c0001t0001g0124 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MFAP5_chr12_8640943_8667826 | MFAP5 | chr12 | 8640943 | 8667826 |
| a0001c0001t0001g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFAP5_chr12_8640943_8667826 | MFAP5 | chr12 | 8640943 | 8667826 |
| a0001c0001t0001g0126 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MFAP5_chr12_8640943_8667826 | MFAP5 | chr12 | 8640943 | 8667826 |
| a0001c0001t0001g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFAP5_chr12_8640943_8667826 | MFAP5 | chr12 | 8640943 | 8667826 |
| a0001c0001t0001g0129 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MFAP5_chr12_8640943_8667826 | MFAP5 | chr12 | 8640943 | 8667826 |
| a0001c0001t0001g0130 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MFAP5_chr12_8640943_8667826 | MFAP5 | chr12 | 8640943 | 8667826 |
| a0001c0001t0001g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFAP5_chr12_8640943_8667826 | MFAP5 | chr12 | 8640943 | 8667826 |
| a0001c0001t0001g0133 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MFAP5_chr12_8640943_8667826 | MFAP5 | chr12 | 8640943 | 8667826 |
| a0001c0001t0001g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFAP5_chr12_8640943_8667826 | MFAP5 | chr12 | 8640943 | 8667826 |
| a0001c0001t0001g0135 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MFAP5_chr12_8640943_8667826 | MFAP5 | chr12 | 8640943 | 8667826 |
| a0001c0001t0001g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFAP5_chr12_8640943_8667826 | MFAP5 | chr12 | 8640943 | 8667826 |
| a0001c0001t0001g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFAP5_chr12_8640943_8667826 | MFAP5 | chr12 | 8640943 | 8667826 |
| a0001c0001t0001g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFAP5_chr12_8640943_8667826 | MFAP5 | chr12 | 8640943 | 8667826 |
| a0001c0001t0001g0139 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MFAP5_chr12_8640943_8667826 | MFAP5 | chr12 | 8640943 | 8667826 |
| a0001c0001t0001g0140 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MFAP5_chr12_8640943_8667826 | MFAP5 | chr12 | 8640943 | 8667826 |
| a0001c0001t0001g0141 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MFAP5_chr12_8640943_8667826 | MFAP5 | chr12 | 8640943 | 8667826 |
| a0001c0001t0001g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFAP5_chr12_8640943_8667826 | MFAP5 | chr12 | 8640943 | 8667826 |
| a0001c0001t0001g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFAP5_chr12_8640943_8667826 | MFAP5 | chr12 | 8640943 | 8667826 |
| a0001c0001t0001g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFAP5_chr12_8640943_8667826 | MFAP5 | chr12 | 8640943 | 8667826 |
| a0001c0001t0001g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFAP5_chr12_8640943_8667826 | MFAP5 | chr12 | 8640943 | 8667826 |
| a0001c0001t0001g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFAP5_chr12_8640943_8667826 | MFAP5 | chr12 | 8640943 | 8667826 |
| a0001c0001t0001g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFAP5_chr12_8640943_8667826 | MFAP5 | chr12 | 8640943 | 8667826 |
| a0001c0001t0001g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFAP5_chr12_8640943_8667826 | MFAP5 | chr12 | 8640943 | 8667826 |
| a0001c0001t0001g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFAP5_chr12_8640943_8667826 | MFAP5 | chr12 | 8640943 | 8667826 |
| a0001c0001t0001g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFAP5_chr12_8640943_8667826 | MFAP5 | chr12 | 8640943 | 8667826 |
| a0001c0001t0001g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFAP5_chr12_8640943_8667826 | MFAP5 | chr12 | 8640943 | 8667826 |
| a0001c0001t0001g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFAP5_chr12_8640943_8667826 | MFAP5 | chr12 | 8640943 | 8667826 |
| a0001c0001t0001g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFAP5_chr12_8640943_8667826 | MFAP5 | chr12 | 8640943 | 8667826 |
| a0001c0001t0001g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFAP5_chr12_8640943_8667826 | MFAP5 | chr12 | 8640943 | 8667826 |
| a0001c0001t0001g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFAP5_chr12_8640943_8667826 | MFAP5 | chr12 | 8640943 | 8667826 |
| a0001c0001t0001g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFAP5_chr12_8640943_8667826 | MFAP5 | chr12 | 8640943 | 8667826 |
| a0001c0001t0001g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFAP5_chr12_8640943_8667826 | MFAP5 | chr12 | 8640943 | 8667826 |
| a0001c0001t0001g0161 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MFAP5_chr12_8640943_8667826 | MFAP5 | chr12 | 8640943 | 8667826 |
| a0001c0001t0001g0162 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MFAP5_chr12_8640943_8667826 | MFAP5 | chr12 | 8640943 | 8667826 |
| a0001c0001t0001g0163 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MFAP5_chr12_8640943_8667826 | MFAP5 | chr12 | 8640943 | 8667826 |
| a0001c0001t0001g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFAP5_chr12_8640943_8667826 | MFAP5 | chr12 | 8640943 | 8667826 |
| a0001c0001t0001g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFAP5_chr12_8640943_8667826 | MFAP5 | chr12 | 8640943 | 8667826 |
| a0001c0001t0001g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFAP5_chr12_8640943_8667826 | MFAP5 | chr12 | 8640943 | 8667826 |
| a0001c0001t0001g0167 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MFAP5_chr12_8640943_8667826 | MFAP5 | chr12 | 8640943 | 8667826 |
| a0001c0001t0001g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFAP5_chr12_8640943_8667826 | MFAP5 | chr12 | 8640943 | 8667826 |
| a0001c0001t0001g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFAP5_chr12_8640943_8667826 | MFAP5 | chr12 | 8640943 | 8667826 |
| a0001c0001t0001g0174 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MFAP5_chr12_8640943_8667826 | MFAP5 | chr12 | 8640943 | 8667826 |
| a0001c0001t0001g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFAP5_chr12_8640943_8667826 | MFAP5 | chr12 | 8640943 | 8667826 |
| a0001c0001t0001g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFAP5_chr12_8640943_8667826 | MFAP5 | chr12 | 8640943 | 8667826 |
| a0001c0001t0001g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFAP5_chr12_8640943_8667826 | MFAP5 | chr12 | 8640943 | 8667826 |
| a0001c0001t0001g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFAP5_chr12_8640943_8667826 | MFAP5 | chr12 | 8640943 | 8667826 |
| a0001c0001t0001g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFAP5_chr12_8640943_8667826 | MFAP5 | chr12 | 8640943 | 8667826 |
| a0001c0001t0001g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFAP5_chr12_8640943_8667826 | MFAP5 | chr12 | 8640943 | 8667826 |
| a0001c0001t0001g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFAP5_chr12_8640943_8667826 | MFAP5 | chr12 | 8640943 | 8667826 |
| a0001c0001t0001g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFAP5_chr12_8640943_8667826 | MFAP5 | chr12 | 8640943 | 8667826 |
| a0001c0001t0001g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFAP5_chr12_8640943_8667826 | MFAP5 | chr12 | 8640943 | 8667826 |
| a0001c0001t0001g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFAP5_chr12_8640943_8667826 | MFAP5 | chr12 | 8640943 | 8667826 |
| a0001c0001t0001g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFAP5_chr12_8640943_8667826 | MFAP5 | chr12 | 8640943 | 8667826 |
| a0001c0001t0001g0188 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MFAP5_chr12_8640943_8667826 | MFAP5 | chr12 | 8640943 | 8667826 |
| a0001c0001t0001g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFAP5_chr12_8640943_8667826 | MFAP5 | chr12 | 8640943 | 8667826 |
| a0001c0001t0001g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFAP5_chr12_8640943_8667826 | MFAP5 | chr12 | 8640943 | 8667826 |
| a0001c0001t0001g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFAP5_chr12_8640943_8667826 | MFAP5 | chr12 | 8640943 | 8667826 |
| a0001c0001t0001g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFAP5_chr12_8640943_8667826 | MFAP5 | chr12 | 8640943 | 8667826 |
| a0001c0001t0001g0193 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MFAP5_chr12_8640943_8667826 | MFAP5 | chr12 | 8640943 | 8667826 |
| a0001c0001t0001g0194 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MFAP5_chr12_8640943_8667826 | MFAP5 | chr12 | 8640943 | 8667826 |
| a0001c0001t0001g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFAP5_chr12_8640943_8667826 | MFAP5 | chr12 | 8640943 | 8667826 |
| a0001c0001t0002g0003 | 0/0 | 11 | 3 | 5 | 0 | 1 | 2 | MFAP5_chr12_8640943_8667826 | MFAP5 | chr12 | 8640943 | 8667826 |
| a0001c0001t0002g0050 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | MFAP5_chr12_8640943_8667826 | MFAP5 | chr12 | 8640943 | 8667826 |
| a0001c0001t0002g0051 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | MFAP5_chr12_8640943_8667826 | MFAP5 | chr12 | 8640943 | 8667826 |
| a0001c0001t0002g0100 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MFAP5_chr12_8640943_8667826 | MFAP5 | chr12 | 8640943 | 8667826 |
| a0001c0001t0002g0104 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MFAP5_chr12_8640943_8667826 | MFAP5 | chr12 | 8640943 | 8667826 |
| a0001c0001t0002g0132 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MFAP5_chr12_8640943_8667826 | MFAP5 | chr12 | 8640943 | 8667826 |
| a0001c0001t0002g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFAP5_chr12_8640943_8667826 | MFAP5 | chr12 | 8640943 | 8667826 |
| a0001c0001t0003g0056 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MFAP5_chr12_8640943_8667826 | MFAP5 | chr12 | 8640943 | 8667826 |
| a0001c0001t0003g0057 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MFAP5_chr12_8640943_8667826 | MFAP5 | chr12 | 8640943 | 8667826 |
| a0001c0001t0003g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFAP5_chr12_8640943_8667826 | MFAP5 | chr12 | 8640943 | 8667826 |
| a0001c0001t0003g0197 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MFAP5_chr12_8640943_8667826 | MFAP5 | chr12 | 8640943 | 8667826 |
| a0001c0001t0003g0198 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MFAP5_chr12_8640943_8667826 | MFAP5 | chr12 | 8640943 | 8667826 |
| a0001c0001t0003g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFAP5_chr12_8640943_8667826 | MFAP5 | chr12 | 8640943 | 8667826 |
| a0001c0001t0003g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFAP5_chr12_8640943_8667826 | MFAP5 | chr12 | 8640943 | 8667826 |
| a0001c0001t0003g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFAP5_chr12_8640943_8667826 | MFAP5 | chr12 | 8640943 | 8667826 |
| a0001c0001t0003g0202 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MFAP5_chr12_8640943_8667826 | MFAP5 | chr12 | 8640943 | 8667826 |
| a0001c0001t0003g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFAP5_chr12_8640943_8667826 | MFAP5 | chr12 | 8640943 | 8667826 |
| a0001c0001t0004g0018 | 0/0 | 3 | 0 | 1 | 0 | 1 | 1 | MFAP5_chr12_8640943_8667826 | MFAP5 | chr12 | 8640943 | 8667826 |
| a0001c0001t0004g0032 | 0/0 | 2 | 0 | 0 | 0 | 1 | 1 | MFAP5_chr12_8640943_8667826 | MFAP5 | chr12 | 8640943 | 8667826 |
| a0001c0001t0004g0033 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | MFAP5_chr12_8640943_8667826 | MFAP5 | chr12 | 8640943 | 8667826 |
| a0001c0001t0004g0060 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MFAP5_chr12_8640943_8667826 | MFAP5 | chr12 | 8640943 | 8667826 |
| a0001c0001t0004g0061 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | MFAP5_chr12_8640943_8667826 | MFAP5 | chr12 | 8640943 | 8667826 |
| a0001c0001t0004g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFAP5_chr12_8640943_8667826 | MFAP5 | chr12 | 8640943 | 8667826 |
| a0001c0001t0004g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MFAP5_chr12_8640943_8667826 | MFAP5 | chr12 | 8640943 | 8667826 |
| a0001c0001t0005g0010 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | MFAP5_chr12_8640943_8667826 | MFAP5 | chr12 | 8640943 | 8667826 |
| a0001c0001t0005g0034 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MFAP5_chr12_8640943_8667826 | MFAP5 | chr12 | 8640943 | 8667826 |
| a0001c0001t0005g0043 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | MFAP5_chr12_8640943_8667826 | MFAP5 | chr12 | 8640943 | 8667826 |
| a0001c0001t0005g0053 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MFAP5_chr12_8640943_8667826 | MFAP5 | chr12 | 8640943 | 8667826 |
| a0001c0001t0006g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFAP5_chr12_8640943_8667826 | MFAP5 | chr12 | 8640943 | 8667826 |
| a0001c0001t0006g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFAP5_chr12_8640943_8667826 | MFAP5 | chr12 | 8640943 | 8667826 |
| a0001c0001t0006g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFAP5_chr12_8640943_8667826 | MFAP5 | chr12 | 8640943 | 8667826 |
| a0001c0001t0006g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFAP5_chr12_8640943_8667826 | MFAP5 | chr12 | 8640943 | 8667826 |
| a0001c0001t0006g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFAP5_chr12_8640943_8667826 | MFAP5 | chr12 | 8640943 | 8667826 |
| a0001c0001t0006g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFAP5_chr12_8640943_8667826 | MFAP5 | chr12 | 8640943 | 8667826 |
| a0001c0001t0007g0014 | 0/0 | 4 | 0 | 4 | 0 | 0 | 0 | MFAP5_chr12_8640943_8667826 | MFAP5 | chr12 | 8640943 | 8667826 |
| a0001c0001t0007g0070 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MFAP5_chr12_8640943_8667826 | MFAP5 | chr12 | 8640943 | 8667826 |
| a0001c0001t0008g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFAP5_chr12_8640943_8667826 | MFAP5 | chr12 | 8640943 | 8667826 |
| a0001c0001t0008g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFAP5_chr12_8640943_8667826 | MFAP5 | chr12 | 8640943 | 8667826 |
| a0001c0001t0008g0062 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MFAP5_chr12_8640943_8667826 | MFAP5 | chr12 | 8640943 | 8667826 |
| a0001c0001t0008g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MFAP5_chr12_8640943_8667826 | MFAP5 | chr12 | 8640943 | 8667826 |
| a0001c0001t0009g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFAP5_chr12_8640943_8667826 | MFAP5 | chr12 | 8640943 | 8667826 |
| a0001c0001t0009g0067 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MFAP5_chr12_8640943_8667826 | MFAP5 | chr12 | 8640943 | 8667826 |
| a0001c0001t0009g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFAP5_chr12_8640943_8667826 | MFAP5 | chr12 | 8640943 | 8667826 |
| a0001c0001t0010g0042 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MFAP5_chr12_8640943_8667826 | MFAP5 | chr12 | 8640943 | 8667826 |
| a0001c0001t0011g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFAP5_chr12_8640943_8667826 | MFAP5 | chr12 | 8640943 | 8667826 |
| a0001c0001t0011g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFAP5_chr12_8640943_8667826 | MFAP5 | chr12 | 8640943 | 8667826 |
| a0001c0001t0012g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFAP5_chr12_8640943_8667826 | MFAP5 | chr12 | 8640943 | 8667826 |
| a0001c0001t0013g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFAP5_chr12_8640943_8667826 | MFAP5 | chr12 | 8640943 | 8667826 |
| a0001c0001t0014g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFAP5_chr12_8640943_8667826 | MFAP5 | chr12 | 8640943 | 8667826 |
| a0001c0001t0015g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFAP5_chr12_8640943_8667826 | MFAP5 | chr12 | 8640943 | 8667826 |
| a0001c0001t0016g0119 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MFAP5_chr12_8640943_8667826 | MFAP5 | chr12 | 8640943 | 8667826 |
| a0001c0001t0017g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFAP5_chr12_8640943_8667826 | MFAP5 | chr12 | 8640943 | 8667826 |
| a0001c0001t0018g0207 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MFAP5_chr12_8640943_8667826 | MFAP5 | chr12 | 8640943 | 8667826 |
| a0001c0003t0012g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFAP5_chr12_8640943_8667826 | MFAP5 | chr12 | 8640943 | 8667826 |
| a0002c0002t0001g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFAP5_chr12_8640943_8667826 | MFAP5 | chr12 | 8640943 | 8667826 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0002 | g0051 | EUR | GBR | MFAP5_chr12_8640943_8667826 | MFAP5 | chr12 | 8640943 | 8667826 |
| HG00099 | hp2 | a0001 | c0001 | t0001 | g0001 | EUR | GBR | MFAP5_chr12_8640943_8667826 | MFAP5 | chr12 | 8640943 | 8667826 |
| HG00140 | hp1 | a0001 | c0001 | t0001 | g0022 | EUR | GBR | MFAP5_chr12_8640943_8667826 | MFAP5 | chr12 | 8640943 | 8667826 |
| HG00140 | hp2 | a0001 | c0001 | t0002 | g0051 | EUR | GBR | MFAP5_chr12_8640943_8667826 | MFAP5 | chr12 | 8640943 | 8667826 |
| HG00280 | hp1 | a0001 | c0001 | t0004 | g0018 | EUR | FIN | MFAP5_chr12_8640943_8667826 | MFAP5 | chr12 | 8640943 | 8667826 |
| HG00280 | hp2 | a0001 | c0001 | t0016 | g0119 | EUR | FIN | MFAP5_chr12_8640943_8667826 | MFAP5 | chr12 | 8640943 | 8667826 |
| HG00323 | hp1 | a0001 | c0001 | t0001 | g0013 | EUR | FIN | MFAP5_chr12_8640943_8667826 | MFAP5 | chr12 | 8640943 | 8667826 |
| HG00323 | hp2 | a0001 | c0001 | t0004 | g0060 | EUR | FIN | MFAP5_chr12_8640943_8667826 | MFAP5 | chr12 | 8640943 | 8667826 |
| HG00408 | hp1 | a0001 | c0001 | t0005 | g0010 | EAS | CHS | MFAP5_chr12_8640943_8667826 | MFAP5 | chr12 | 8640943 | 8667826 |
| HG00408 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | CHS | MFAP5_chr12_8640943_8667826 | MFAP5 | chr12 | 8640943 | 8667826 |
| HG00423 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | MFAP5_chr12_8640943_8667826 | MFAP5 | chr12 | 8640943 | 8667826 |
| HG00423 | hp2 | a0001 | c0001 | t0005 | g0010 | EAS | CHS | MFAP5_chr12_8640943_8667826 | MFAP5 | chr12 | 8640943 | 8667826 |
| HG00438 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | MFAP5_chr12_8640943_8667826 | MFAP5 | chr12 | 8640943 | 8667826 |
| HG00438 | hp2 | a0001 | c0001 | t0001 | g0045 | EAS | CHS | MFAP5_chr12_8640943_8667826 | MFAP5 | chr12 | 8640943 | 8667826 |
| HG00544 | hp1 | a0001 | c0001 | t0001 | g0009 | EAS | CHS | MFAP5_chr12_8640943_8667826 | MFAP5 | chr12 | 8640943 | 8667826 |
| HG00544 | hp2 | a0001 | c0001 | t0001 | g0017 | EAS | CHS | MFAP5_chr12_8640943_8667826 | MFAP5 | chr12 | 8640943 | 8667826 |
| HG00558 | hp1 | a0001 | c0001 | t0001 | g0099 | EAS | CHS | MFAP5_chr12_8640943_8667826 | MFAP5 | chr12 | 8640943 | 8667826 |
| HG00558 | hp2 | a0001 | c0001 | t0001 | g0025 | EAS | CHS | MFAP5_chr12_8640943_8667826 | MFAP5 | chr12 | 8640943 | 8667826 |
| HG00597 | hp1 | a0001 | c0001 | t0001 | g0031 | EAS | CHS | MFAP5_chr12_8640943_8667826 | MFAP5 | chr12 | 8640943 | 8667826 |
| HG00597 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | MFAP5_chr12_8640943_8667826 | MFAP5 | chr12 | 8640943 | 8667826 |
| HG00609 | hp1 | a0001 | c0001 | t0001 | g0009 | EAS | CHS | MFAP5_chr12_8640943_8667826 | MFAP5 | chr12 | 8640943 | 8667826 |
| HG00609 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | CHS | MFAP5_chr12_8640943_8667826 | MFAP5 | chr12 | 8640943 | 8667826 |
| HG00621 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | CHS | MFAP5_chr12_8640943_8667826 | MFAP5 | chr12 | 8640943 | 8667826 |
| HG00621 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | MFAP5_chr12_8640943_8667826 | MFAP5 | chr12 | 8640943 | 8667826 |
| HG00639 | hp1 | a0001 | c0001 | t0002 | g0132 | AMR | PUR | MFAP5_chr12_8640943_8667826 | MFAP5 | chr12 | 8640943 | 8667826 |
| HG00639 | hp2 | a0001 | c0001 | t0001 | g0163 | AMR | PUR | MFAP5_chr12_8640943_8667826 | MFAP5 | chr12 | 8640943 | 8667826 |
| HG00673 | hp1 | a0001 | c0001 | t0001 | g0115 | EAS | CHS | MFAP5_chr12_8640943_8667826 | MFAP5 | chr12 | 8640943 | 8667826 |
| HG00673 | hp2 | a0001 | c0001 | t0001 | g0108 | EAS | CHS | MFAP5_chr12_8640943_8667826 | MFAP5 | chr12 | 8640943 | 8667826 |
| HG00735 | hp1 | a0001 | c0001 | t0001 | g0072 | AMR | PUR | MFAP5_chr12_8640943_8667826 | MFAP5 | chr12 | 8640943 | 8667826 |
| HG00735 | hp2 | a0001 | c0001 | t0002 | g0003 | AMR | PUR | MFAP5_chr12_8640943_8667826 | MFAP5 | chr12 | 8640943 | 8667826 |
| HG00738 | hp1 | a0001 | c0001 | t0007 | g0014 | AMR | PUR | MFAP5_chr12_8640943_8667826 | MFAP5 | chr12 | 8640943 | 8667826 |
| HG00738 | hp2 | a0001 | c0001 | t0002 | g0104 | AMR | PUR | MFAP5_chr12_8640943_8667826 | MFAP5 | chr12 | 8640943 | 8667826 |
| HG01071 | hp1 | a0001 | c0001 | t0007 | g0070 | AMR | PUR | MFAP5_chr12_8640943_8667826 | MFAP5 | chr12 | 8640943 | 8667826 |
| HG01071 | hp2 | a0001 | c0001 | t0001 | g0133 | AMR | PUR | MFAP5_chr12_8640943_8667826 | MFAP5 | chr12 | 8640943 | 8667826 |
| HG01074 | hp1 | a0001 | c0001 | t0002 | g0050 | AMR | PUR | MFAP5_chr12_8640943_8667826 | MFAP5 | chr12 | 8640943 | 8667826 |
| HG01074 | hp2 | a0001 | c0001 | t0001 | g0028 | AMR | PUR | MFAP5_chr12_8640943_8667826 | MFAP5 | chr12 | 8640943 | 8667826 |
| HG01081 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | MFAP5_chr12_8640943_8667826 | MFAP5 | chr12 | 8640943 | 8667826 |
| HG01081 | hp2 | a0001 | c0001 | t0002 | g0003 | AMR | PUR | MFAP5_chr12_8640943_8667826 | MFAP5 | chr12 | 8640943 | 8667826 |
| HG01099 | hp1 | a0001 | c0001 | t0002 | g0050 | AMR | PUR | MFAP5_chr12_8640943_8667826 | MFAP5 | chr12 | 8640943 | 8667826 |
| HG01099 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | MFAP5_chr12_8640943_8667826 | MFAP5 | chr12 | 8640943 | 8667826 |
| HG01106 | hp1 | a0001 | c0001 | t0001 | g0004 | AMR | PUR | MFAP5_chr12_8640943_8667826 | MFAP5 | chr12 | 8640943 | 8667826 |
| HG01106 | hp2 | a0001 | c0001 | t0001 | g0027 | AMR | PUR | MFAP5_chr12_8640943_8667826 | MFAP5 | chr12 | 8640943 | 8667826 |
| HG01109 | hp1 | a0001 | c0001 | t0001 | g0140 | AMR | PUR | MFAP5_chr12_8640943_8667826 | MFAP5 | chr12 | 8640943 | 8667826 |
| HG01109 | hp2 | a0001 | c0001 | t0001 | g0004 | AMR | PUR | MFAP5_chr12_8640943_8667826 | MFAP5 | chr12 | 8640943 | 8667826 |
| HG01167 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | MFAP5_chr12_8640943_8667826 | MFAP5 | chr12 | 8640943 | 8667826 |
| HG01167 | hp2 | a0001 | c0001 | t0002 | g0003 | AMR | PUR | MFAP5_chr12_8640943_8667826 | MFAP5 | chr12 | 8640943 | 8667826 |
| HG01168 | hp1 | a0001 | c0001 | t0001 | g0083 | AMR | PUR | MFAP5_chr12_8640943_8667826 | MFAP5 | chr12 | 8640943 | 8667826 |
| HG01168 | hp2 | a0001 | c0001 | t0003 | g0202 | AMR | PUR | MFAP5_chr12_8640943_8667826 | MFAP5 | chr12 | 8640943 | 8667826 |
| HG01169 | hp1 | a0001 | c0001 | t0003 | g0198 | AMR | PUR | MFAP5_chr12_8640943_8667826 | MFAP5 | chr12 | 8640943 | 8667826 |
| HG01169 | hp2 | a0001 | c0001 | t0001 | g0026 | AMR | PUR | MFAP5_chr12_8640943_8667826 | MFAP5 | chr12 | 8640943 | 8667826 |
| HG01175 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | MFAP5_chr12_8640943_8667826 | MFAP5 | chr12 | 8640943 | 8667826 |
| HG01175 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | MFAP5_chr12_8640943_8667826 | MFAP5 | chr12 | 8640943 | 8667826 |
| HG01192 | hp1 | a0001 | c0001 | t0001 | g0035 | AMR | PUR | MFAP5_chr12_8640943_8667826 | MFAP5 | chr12 | 8640943 | 8667826 |
| HG01192 | hp2 | a0001 | c0001 | t0001 | g0110 | AMR | PUR | MFAP5_chr12_8640943_8667826 | MFAP5 | chr12 | 8640943 | 8667826 |
| HG01243 | hp1 | a0001 | c0001 | t0001 | g0035 | AMR | PUR | MFAP5_chr12_8640943_8667826 | MFAP5 | chr12 | 8640943 | 8667826 |
| HG01243 | hp2 | a0001 | c0001 | t0001 | g0046 | AMR | PUR | MFAP5_chr12_8640943_8667826 | MFAP5 | chr12 | 8640943 | 8667826 |
| HG01255 | hp1 | a0001 | c0001 | t0002 | g0003 | AMR | CLM | MFAP5_chr12_8640943_8667826 | MFAP5 | chr12 | 8640943 | 8667826 |
| HG01255 | hp2 | a0001 | c0001 | t0001 | g0022 | AMR | CLM | MFAP5_chr12_8640943_8667826 | MFAP5 | chr12 | 8640943 | 8667826 |
| HG01256 | hp1 | a0001 | c0001 | t0001 | g0073 | AMR | CLM | MFAP5_chr12_8640943_8667826 | MFAP5 | chr12 | 8640943 | 8667826 |
| HG01256 | hp2 | a0001 | c0001 | t0007 | g0014 | AMR | CLM | MFAP5_chr12_8640943_8667826 | MFAP5 | chr12 | 8640943 | 8667826 |
| HG01257 | hp1 | a0001 | c0001 | t0001 | g0029 | AMR | CLM | MFAP5_chr12_8640943_8667826 | MFAP5 | chr12 | 8640943 | 8667826 |
| HG01257 | hp2 | a0001 | c0001 | t0004 | g0065 | AMR | CLM | MFAP5_chr12_8640943_8667826 | MFAP5 | chr12 | 8640943 | 8667826 |
| HG01258 | hp1 | a0001 | c0001 | t0004 | g0033 | AMR | CLM | MFAP5_chr12_8640943_8667826 | MFAP5 | chr12 | 8640943 | 8667826 |
| HG01258 | hp2 | a0001 | c0001 | t0007 | g0014 | AMR | CLM | MFAP5_chr12_8640943_8667826 | MFAP5 | chr12 | 8640943 | 8667826 |
| HG01261 | hp1 | a0001 | c0001 | t0003 | g0197 | AMR | CLM | MFAP5_chr12_8640943_8667826 | MFAP5 | chr12 | 8640943 | 8667826 |
| HG01261 | hp2 | a0001 | c0001 | t0001 | g0090 | AMR | CLM | MFAP5_chr12_8640943_8667826 | MFAP5 | chr12 | 8640943 | 8667826 |
| HG01346 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | MFAP5_chr12_8640943_8667826 | MFAP5 | chr12 | 8640943 | 8667826 |
| HG01346 | hp2 | a0001 | c0001 | t0001 | g0004 | AMR | CLM | MFAP5_chr12_8640943_8667826 | MFAP5 | chr12 | 8640943 | 8667826 |
| HG01358 | hp1 | a0001 | c0001 | t0004 | g0033 | AMR | CLM | MFAP5_chr12_8640943_8667826 | MFAP5 | chr12 | 8640943 | 8667826 |
| HG01358 | hp2 | a0001 | c0001 | t0002 | g0003 | AMR | CLM | MFAP5_chr12_8640943_8667826 | MFAP5 | chr12 | 8640943 | 8667826 |
| HG01361 | hp1 | a0001 | c0001 | t0001 | g0025 | AMR | CLM | MFAP5_chr12_8640943_8667826 | MFAP5 | chr12 | 8640943 | 8667826 |
| HG01361 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | CLM | MFAP5_chr12_8640943_8667826 | MFAP5 | chr12 | 8640943 | 8667826 |
| HG01433 | hp1 | a0001 | c0001 | t0001 | g0004 | AMR | CLM | MFAP5_chr12_8640943_8667826 | MFAP5 | chr12 | 8640943 | 8667826 |
| HG01433 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | MFAP5_chr12_8640943_8667826 | MFAP5 | chr12 | 8640943 | 8667826 |
| HG01496 | hp1 | a0001 | c0001 | t0001 | g0129 | AMR | CLM | MFAP5_chr12_8640943_8667826 | MFAP5 | chr12 | 8640943 | 8667826 |
| HG01496 | hp2 | a0001 | c0001 | t0007 | g0014 | AMR | CLM | MFAP5_chr12_8640943_8667826 | MFAP5 | chr12 | 8640943 | 8667826 |
| HG01515 | hp1 | a0001 | c0001 | t0001 | g0001 | EUR | IBS | MFAP5_chr12_8640943_8667826 | MFAP5 | chr12 | 8640943 | 8667826 |
| HG01515 | hp2 | a0001 | c0001 | t0002 | g0003 | EUR | IBS | MFAP5_chr12_8640943_8667826 | MFAP5 | chr12 | 8640943 | 8667826 |
| HG01884 | hp1 | a0001 | c0001 | t0001 | g0157 | AFR | ACB | MFAP5_chr12_8640943_8667826 | MFAP5 | chr12 | 8640943 | 8667826 |
| HG01884 | hp2 | a0001 | c0001 | t0001 | g0007 | AFR | ACB | MFAP5_chr12_8640943_8667826 | MFAP5 | chr12 | 8640943 | 8667826 |
| HG01891 | hp1 | a0001 | c0001 | t0006 | g0084 | AFR | ACB | MFAP5_chr12_8640943_8667826 | MFAP5 | chr12 | 8640943 | 8667826 |
| HG01891 | hp2 | a0001 | c0001 | t0001 | g0016 | AFR | ACB | MFAP5_chr12_8640943_8667826 | MFAP5 | chr12 | 8640943 | 8667826 |
| HG01928 | hp1 | a0001 | c0001 | t0008 | g0063 | AMR | PEL | MFAP5_chr12_8640943_8667826 | MFAP5 | chr12 | 8640943 | 8667826 |
| HG01928 | hp2 | a0001 | c0001 | t0001 | g0076 | AMR | PEL | MFAP5_chr12_8640943_8667826 | MFAP5 | chr12 | 8640943 | 8667826 |
| HG01934 | hp1 | a0001 | c0001 | t0008 | g0062 | AMR | PEL | MFAP5_chr12_8640943_8667826 | MFAP5 | chr12 | 8640943 | 8667826 |
| HG01934 | hp2 | a0001 | c0001 | t0001 | g0009 | AMR | PEL | MFAP5_chr12_8640943_8667826 | MFAP5 | chr12 | 8640943 | 8667826 |
| HG01952 | hp1 | a0001 | c0001 | t0001 | g0013 | AMR | PEL | MFAP5_chr12_8640943_8667826 | MFAP5 | chr12 | 8640943 | 8667826 |
| HG01952 | hp2 | a0001 | c0001 | t0001 | g0086 | AMR | PEL | MFAP5_chr12_8640943_8667826 | MFAP5 | chr12 | 8640943 | 8667826 |
| HG01978 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | MFAP5_chr12_8640943_8667826 | MFAP5 | chr12 | 8640943 | 8667826 |
| HG01978 | hp2 | a0001 | c0001 | t0001 | g0004 | AMR | PEL | MFAP5_chr12_8640943_8667826 | MFAP5 | chr12 | 8640943 | 8667826 |
| HG01981 | hp1 | a0001 | c0001 | t0001 | g0027 | AMR | PEL | MFAP5_chr12_8640943_8667826 | MFAP5 | chr12 | 8640943 | 8667826 |
| HG01981 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | MFAP5_chr12_8640943_8667826 | MFAP5 | chr12 | 8640943 | 8667826 |
| HG01993 | hp1 | a0001 | c0001 | t0001 | g0174 | AMR | PEL | MFAP5_chr12_8640943_8667826 | MFAP5 | chr12 | 8640943 | 8667826 |
| HG01993 | hp2 | a0001 | c0001 | t0001 | g0012 | AMR | PEL | MFAP5_chr12_8640943_8667826 | MFAP5 | chr12 | 8640943 | 8667826 |
| HG02004 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | MFAP5_chr12_8640943_8667826 | MFAP5 | chr12 | 8640943 | 8667826 |
| HG02004 | hp2 | a0001 | c0001 | t0001 | g0102 | AMR | PEL | MFAP5_chr12_8640943_8667826 | MFAP5 | chr12 | 8640943 | 8667826 |
| HG02015 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | MFAP5_chr12_8640943_8667826 | MFAP5 | chr12 | 8640943 | 8667826 |
| HG02015 | hp2 | a0001 | c0001 | t0001 | g0030 | EAS | KHV | MFAP5_chr12_8640943_8667826 | MFAP5 | chr12 | 8640943 | 8667826 |
| HG02027 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | KHV | MFAP5_chr12_8640943_8667826 | MFAP5 | chr12 | 8640943 | 8667826 |
| HG02027 | hp2 | a0001 | c0001 | t0001 | g0092 | EAS | KHV | MFAP5_chr12_8640943_8667826 | MFAP5 | chr12 | 8640943 | 8667826 |
| HG02040 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | KHV | MFAP5_chr12_8640943_8667826 | MFAP5 | chr12 | 8640943 | 8667826 |
| HG02040 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | KHV | MFAP5_chr12_8640943_8667826 | MFAP5 | chr12 | 8640943 | 8667826 |
| HG02055 | hp1 | a0001 | c0001 | t0003 | g0056 | AFR | ACB | MFAP5_chr12_8640943_8667826 | MFAP5 | chr12 | 8640943 | 8667826 |
| HG02055 | hp2 | a0001 | c0001 | t0001 | g0169 | AFR | ACB | MFAP5_chr12_8640943_8667826 | MFAP5 | chr12 | 8640943 | 8667826 |
| HG02056 | hp1 | a0002 | c0002 | t0001 | g0144 | EAS | KHV | MFAP5_chr12_8640943_8667826 | MFAP5 | chr12 | 8640943 | 8667826 |
| HG02056 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | KHV | MFAP5_chr12_8640943_8667826 | MFAP5 | chr12 | 8640943 | 8667826 |
| HG02074 | hp1 | a0001 | c0001 | t0001 | g0029 | EAS | KHV | MFAP5_chr12_8640943_8667826 | MFAP5 | chr12 | 8640943 | 8667826 |
| HG02074 | hp2 | a0001 | c0001 | t0005 | g0010 | EAS | KHV | MFAP5_chr12_8640943_8667826 | MFAP5 | chr12 | 8640943 | 8667826 |
| HG02080 | hp1 | a0001 | c0001 | t0001 | g0031 | EAS | KHV | MFAP5_chr12_8640943_8667826 | MFAP5 | chr12 | 8640943 | 8667826 |
| HG02080 | hp2 | a0001 | c0001 | t0001 | g0125 | EAS | KHV | MFAP5_chr12_8640943_8667826 | MFAP5 | chr12 | 8640943 | 8667826 |
| HG02083 | hp1 | a0001 | c0001 | t0001 | g0017 | EAS | KHV | MFAP5_chr12_8640943_8667826 | MFAP5 | chr12 | 8640943 | 8667826 |
| HG02083 | hp2 | a0001 | c0001 | t0001 | g0107 | EAS | KHV | MFAP5_chr12_8640943_8667826 | MFAP5 | chr12 | 8640943 | 8667826 |
| HG02129 | hp1 | a0001 | c0001 | t0001 | g0192 | EAS | KHV | MFAP5_chr12_8640943_8667826 | MFAP5 | chr12 | 8640943 | 8667826 |
| HG02129 | hp2 | a0001 | c0001 | t0001 | g0029 | EAS | KHV | MFAP5_chr12_8640943_8667826 | MFAP5 | chr12 | 8640943 | 8667826 |
| HG02132 | hp1 | a0001 | c0001 | t0001 | g0008 | EAS | KHV | MFAP5_chr12_8640943_8667826 | MFAP5 | chr12 | 8640943 | 8667826 |
| HG02132 | hp2 | a0001 | c0001 | t0001 | g0054 | EAS | KHV | MFAP5_chr12_8640943_8667826 | MFAP5 | chr12 | 8640943 | 8667826 |
| HG02145 | hp1 | a0001 | c0001 | t0003 | g0056 | AFR | ACB | MFAP5_chr12_8640943_8667826 | MFAP5 | chr12 | 8640943 | 8667826 |
| HG02145 | hp2 | a0001 | c0001 | t0001 | g0089 | AFR | ACB | MFAP5_chr12_8640943_8667826 | MFAP5 | chr12 | 8640943 | 8667826 |
| HG02165 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CDX | MFAP5_chr12_8640943_8667826 | MFAP5 | chr12 | 8640943 | 8667826 |
| HG02165 | hp2 | a0001 | c0001 | t0001 | g0113 | EAS | CDX | MFAP5_chr12_8640943_8667826 | MFAP5 | chr12 | 8640943 | 8667826 |
| HG02257 | hp1 | a0001 | c0001 | t0001 | g0153 | AFR | ACB | MFAP5_chr12_8640943_8667826 | MFAP5 | chr12 | 8640943 | 8667826 |
| HG02257 | hp2 | a0001 | c0001 | t0001 | g0154 | AFR | ACB | MFAP5_chr12_8640943_8667826 | MFAP5 | chr12 | 8640943 | 8667826 |
| HG02258 | hp1 | a0001 | c0001 | t0001 | g0127 | AFR | ACB | MFAP5_chr12_8640943_8667826 | MFAP5 | chr12 | 8640943 | 8667826 |
| HG02258 | hp2 | a0001 | c0001 | t0008 | g0059 | AFR | ACB | MFAP5_chr12_8640943_8667826 | MFAP5 | chr12 | 8640943 | 8667826 |
| HG02273 | hp1 | a0001 | c0001 | t0001 | g0027 | AMR | PEL | MFAP5_chr12_8640943_8667826 | MFAP5 | chr12 | 8640943 | 8667826 |
| HG02273 | hp2 | a0001 | c0001 | t0001 | g0013 | AMR | PEL | MFAP5_chr12_8640943_8667826 | MFAP5 | chr12 | 8640943 | 8667826 |
| HG02280 | hp1 | a0001 | c0001 | t0001 | g0016 | AFR | ACB | MFAP5_chr12_8640943_8667826 | MFAP5 | chr12 | 8640943 | 8667826 |
| HG02280 | hp2 | a0001 | c0001 | t0001 | g0021 | AFR | ACB | MFAP5_chr12_8640943_8667826 | MFAP5 | chr12 | 8640943 | 8667826 |
| HG02300 | hp1 | a0001 | c0001 | t0001 | g0038 | AMR | PEL | MFAP5_chr12_8640943_8667826 | MFAP5 | chr12 | 8640943 | 8667826 |
| HG02300 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | PEL | MFAP5_chr12_8640943_8667826 | MFAP5 | chr12 | 8640943 | 8667826 |
| HG02451 | hp1 | a0001 | c0001 | t0001 | g0021 | AFR | ACB | MFAP5_chr12_8640943_8667826 | MFAP5 | chr12 | 8640943 | 8667826 |
| HG02451 | hp2 | a0001 | c0001 | t0002 | g0003 | AFR | ACB | MFAP5_chr12_8640943_8667826 | MFAP5 | chr12 | 8640943 | 8667826 |
| HG02523 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | KHV | MFAP5_chr12_8640943_8667826 | MFAP5 | chr12 | 8640943 | 8667826 |
| HG02523 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | KHV | MFAP5_chr12_8640943_8667826 | MFAP5 | chr12 | 8640943 | 8667826 |
| HG02572 | hp1 | a0001 | c0001 | t0001 | g0152 | AFR | GWD | MFAP5_chr12_8640943_8667826 | MFAP5 | chr12 | 8640943 | 8667826 |
| HG02572 | hp2 | a0001 | c0001 | t0012 | g0205 | AFR | GWD | MFAP5_chr12_8640943_8667826 | MFAP5 | chr12 | 8640943 | 8667826 |
| HG02602 | hp1 | a0001 | c0001 | t0001 | g0101 | SAS | PJL | MFAP5_chr12_8640943_8667826 | MFAP5 | chr12 | 8640943 | 8667826 |
| HG02602 | hp2 | a0001 | c0001 | t0001 | g0047 | SAS | PJL | MFAP5_chr12_8640943_8667826 | MFAP5 | chr12 | 8640943 | 8667826 |
| HG02615 | hp1 | a0001 | c0001 | t0001 | g0087 | AFR | GWD | MFAP5_chr12_8640943_8667826 | MFAP5 | chr12 | 8640943 | 8667826 |
| HG02615 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | GWD | MFAP5_chr12_8640943_8667826 | MFAP5 | chr12 | 8640943 | 8667826 |
| HG02622 | hp1 | a0001 | c0001 | t0001 | g0041 | AFR | GWD | MFAP5_chr12_8640943_8667826 | MFAP5 | chr12 | 8640943 | 8667826 |
| HG02622 | hp2 | a0001 | c0001 | t0006 | g0172 | AFR | GWD | MFAP5_chr12_8640943_8667826 | MFAP5 | chr12 | 8640943 | 8667826 |
| HG02630 | hp1 | a0001 | c0001 | t0001 | g0016 | AFR | GWD | MFAP5_chr12_8640943_8667826 | MFAP5 | chr12 | 8640943 | 8667826 |
| HG02630 | hp2 | a0001 | c0001 | t0001 | g0011 | AFR | GWD | MFAP5_chr12_8640943_8667826 | MFAP5 | chr12 | 8640943 | 8667826 |
| HG02647 | hp1 | a0001 | c0001 | t0001 | g0022 | AFR | GWD | MFAP5_chr12_8640943_8667826 | MFAP5 | chr12 | 8640943 | 8667826 |
| HG02647 | hp2 | a0001 | c0001 | t0001 | g0007 | AFR | GWD | MFAP5_chr12_8640943_8667826 | MFAP5 | chr12 | 8640943 | 8667826 |
| HG02683 | hp1 | a0001 | c0001 | t0001 | g0005 | SAS | PJL | MFAP5_chr12_8640943_8667826 | MFAP5 | chr12 | 8640943 | 8667826 |
| HG02683 | hp2 | a0001 | c0001 | t0001 | g0081 | SAS | PJL | MFAP5_chr12_8640943_8667826 | MFAP5 | chr12 | 8640943 | 8667826 |
| HG02698 | hp1 | a0001 | c0001 | t0001 | g0038 | SAS | PJL | MFAP5_chr12_8640943_8667826 | MFAP5 | chr12 | 8640943 | 8667826 |
| HG02698 | hp2 | a0001 | c0001 | t0004 | g0018 | SAS | PJL | MFAP5_chr12_8640943_8667826 | MFAP5 | chr12 | 8640943 | 8667826 |
| HG02717 | hp1 | a0001 | c0001 | t0006 | g0105 | AFR | GWD | MFAP5_chr12_8640943_8667826 | MFAP5 | chr12 | 8640943 | 8667826 |
| HG02717 | hp2 | a0001 | c0001 | t0001 | g0012 | AFR | GWD | MFAP5_chr12_8640943_8667826 | MFAP5 | chr12 | 8640943 | 8667826 |
| HG02723 | hp1 | a0001 | c0001 | t0001 | g0011 | AFR | GWD | MFAP5_chr12_8640943_8667826 | MFAP5 | chr12 | 8640943 | 8667826 |
| HG02723 | hp2 | a0001 | c0001 | t0005 | g0034 | AFR | GWD | MFAP5_chr12_8640943_8667826 | MFAP5 | chr12 | 8640943 | 8667826 |
| HG02735 | hp1 | a0001 | c0001 | t0001 | g0118 | SAS | PJL | MFAP5_chr12_8640943_8667826 | MFAP5 | chr12 | 8640943 | 8667826 |
| HG02735 | hp2 | a0001 | c0001 | t0001 | g0039 | SAS | PJL | MFAP5_chr12_8640943_8667826 | MFAP5 | chr12 | 8640943 | 8667826 |
| HG02738 | hp1 | a0001 | c0001 | t0001 | g0093 | SAS | PJL | MFAP5_chr12_8640943_8667826 | MFAP5 | chr12 | 8640943 | 8667826 |
| HG02738 | hp2 | a0001 | c0001 | t0001 | g0135 | SAS | PJL | MFAP5_chr12_8640943_8667826 | MFAP5 | chr12 | 8640943 | 8667826 |
| HG02809 | hp1 | a0001 | c0001 | t0001 | g0055 | AFR | GWD | MFAP5_chr12_8640943_8667826 | MFAP5 | chr12 | 8640943 | 8667826 |
| HG02809 | hp2 | a0001 | c0001 | t0006 | g0171 | AFR | GWD | MFAP5_chr12_8640943_8667826 | MFAP5 | chr12 | 8640943 | 8667826 |
| HG02886 | hp1 | a0001 | c0001 | t0001 | g0151 | AFR | GWD | MFAP5_chr12_8640943_8667826 | MFAP5 | chr12 | 8640943 | 8667826 |
| HG02886 | hp2 | a0001 | c0001 | t0001 | g0012 | AFR | GWD | MFAP5_chr12_8640943_8667826 | MFAP5 | chr12 | 8640943 | 8667826 |
| HG02896 | hp1 | a0001 | c0001 | t0001 | g0160 | AFR | GWD | MFAP5_chr12_8640943_8667826 | MFAP5 | chr12 | 8640943 | 8667826 |
| HG02896 | hp2 | a0001 | c0001 | t0001 | g0015 | AFR | GWD | MFAP5_chr12_8640943_8667826 | MFAP5 | chr12 | 8640943 | 8667826 |
| HG02922 | hp1 | a0001 | c0001 | t0001 | g0015 | AFR | ESN | MFAP5_chr12_8640943_8667826 | MFAP5 | chr12 | 8640943 | 8667826 |
| HG02922 | hp2 | a0001 | c0001 | t0001 | g0021 | AFR | ESN | MFAP5_chr12_8640943_8667826 | MFAP5 | chr12 | 8640943 | 8667826 |
| HG02965 | hp1 | a0001 | c0001 | t0006 | g0170 | AFR | ESN | MFAP5_chr12_8640943_8667826 | MFAP5 | chr12 | 8640943 | 8667826 |
| HG02965 | hp2 | a0001 | c0001 | t0003 | g0057 | AFR | ESN | MFAP5_chr12_8640943_8667826 | MFAP5 | chr12 | 8640943 | 8667826 |
| HG02970 | hp1 | a0001 | c0003 | t0012 | g0203 | AFR | ESN | MFAP5_chr12_8640943_8667826 | MFAP5 | chr12 | 8640943 | 8667826 |
| HG02970 | hp2 | a0001 | c0001 | t0003 | g0201 | AFR | ESN | MFAP5_chr12_8640943_8667826 | MFAP5 | chr12 | 8640943 | 8667826 |
| HG02976 | hp1 | a0001 | c0001 | t0002 | g0003 | AFR | ESN | MFAP5_chr12_8640943_8667826 | MFAP5 | chr12 | 8640943 | 8667826 |
| HG02976 | hp2 | a0001 | c0001 | t0010 | g0042 | AFR | ESN | MFAP5_chr12_8640943_8667826 | MFAP5 | chr12 | 8640943 | 8667826 |
| HG03017 | hp1 | a0001 | c0001 | t0001 | g0085 | SAS | PJL | MFAP5_chr12_8640943_8667826 | MFAP5 | chr12 | 8640943 | 8667826 |
| HG03017 | hp2 | a0001 | c0001 | t0001 | g0193 | SAS | PJL | MFAP5_chr12_8640943_8667826 | MFAP5 | chr12 | 8640943 | 8667826 |
| HG03041 | hp1 | a0001 | c0001 | t0001 | g0041 | AFR | GWD | MFAP5_chr12_8640943_8667826 | MFAP5 | chr12 | 8640943 | 8667826 |
| HG03041 | hp2 | a0001 | c0001 | t0001 | g0028 | AFR | GWD | MFAP5_chr12_8640943_8667826 | MFAP5 | chr12 | 8640943 | 8667826 |
| HG03098 | hp1 | a0001 | c0001 | t0017 | g0204 | AFR | MSL | MFAP5_chr12_8640943_8667826 | MFAP5 | chr12 | 8640943 | 8667826 |
| HG03098 | hp2 | a0001 | c0001 | t0001 | g0146 | AFR | MSL | MFAP5_chr12_8640943_8667826 | MFAP5 | chr12 | 8640943 | 8667826 |
| HG03130 | hp1 | a0001 | c0001 | t0003 | g0200 | AFR | ESN | MFAP5_chr12_8640943_8667826 | MFAP5 | chr12 | 8640943 | 8667826 |
| HG03130 | hp2 | a0001 | c0001 | t0001 | g0007 | AFR | ESN | MFAP5_chr12_8640943_8667826 | MFAP5 | chr12 | 8640943 | 8667826 |
| HG03139 | hp1 | a0001 | c0001 | t0005 | g0034 | AFR | ESN | MFAP5_chr12_8640943_8667826 | MFAP5 | chr12 | 8640943 | 8667826 |
| HG03139 | hp2 | a0001 | c0001 | t0005 | g0053 | AFR | ESN | MFAP5_chr12_8640943_8667826 | MFAP5 | chr12 | 8640943 | 8667826 |
| HG03195 | hp1 | a0001 | c0001 | t0001 | g0040 | AFR | ESN | MFAP5_chr12_8640943_8667826 | MFAP5 | chr12 | 8640943 | 8667826 |
| HG03195 | hp2 | a0001 | c0001 | t0003 | g0206 | AFR | ESN | MFAP5_chr12_8640943_8667826 | MFAP5 | chr12 | 8640943 | 8667826 |
| HG03209 | hp1 | a0001 | c0001 | t0008 | g0058 | AFR | MSL | MFAP5_chr12_8640943_8667826 | MFAP5 | chr12 | 8640943 | 8667826 |
| HG03209 | hp2 | a0001 | c0001 | t0004 | g0064 | AFR | MSL | MFAP5_chr12_8640943_8667826 | MFAP5 | chr12 | 8640943 | 8667826 |
| HG03225 | hp1 | a0001 | c0001 | t0001 | g0111 | AFR | MSL | MFAP5_chr12_8640943_8667826 | MFAP5 | chr12 | 8640943 | 8667826 |
| HG03225 | hp2 | a0001 | c0001 | t0003 | g0196 | AFR | MSL | MFAP5_chr12_8640943_8667826 | MFAP5 | chr12 | 8640943 | 8667826 |
| HG03239 | hp1 | a0001 | c0001 | t0001 | g0046 | SAS | PJL | MFAP5_chr12_8640943_8667826 | MFAP5 | chr12 | 8640943 | 8667826 |
| HG03239 | hp2 | a0001 | c0001 | t0001 | g0194 | SAS | PJL | MFAP5_chr12_8640943_8667826 | MFAP5 | chr12 | 8640943 | 8667826 |
| HG03453 | hp1 | a0001 | c0001 | t0001 | g0002 | AFR | MSL | MFAP5_chr12_8640943_8667826 | MFAP5 | chr12 | 8640943 | 8667826 |
| HG03453 | hp2 | a0001 | c0001 | t0001 | g0040 | AFR | MSL | MFAP5_chr12_8640943_8667826 | MFAP5 | chr12 | 8640943 | 8667826 |
| HG03490 | hp1 | a0001 | c0001 | t0001 | g0052 | SAS | PJL | MFAP5_chr12_8640943_8667826 | MFAP5 | chr12 | 8640943 | 8667826 |
| HG03490 | hp2 | a0001 | c0001 | t0002 | g0003 | SAS | PJL | MFAP5_chr12_8640943_8667826 | MFAP5 | chr12 | 8640943 | 8667826 |
| HG03491 | hp1 | a0001 | c0001 | t0001 | g0161 | SAS | PJL | MFAP5_chr12_8640943_8667826 | MFAP5 | chr12 | 8640943 | 8667826 |
| HG03491 | hp2 | a0001 | c0001 | t0001 | g0167 | SAS | PJL | MFAP5_chr12_8640943_8667826 | MFAP5 | chr12 | 8640943 | 8667826 |
| HG03492 | hp1 | a0001 | c0001 | t0001 | g0002 | SAS | PJL | MFAP5_chr12_8640943_8667826 | MFAP5 | chr12 | 8640943 | 8667826 |
| HG03492 | hp2 | a0001 | c0001 | t0002 | g0003 | SAS | PJL | MFAP5_chr12_8640943_8667826 | MFAP5 | chr12 | 8640943 | 8667826 |
| HG03516 | hp1 | a0001 | c0001 | t0011 | g0175 | AFR | ESN | MFAP5_chr12_8640943_8667826 | MFAP5 | chr12 | 8640943 | 8667826 |
| HG03516 | hp2 | a0001 | c0001 | t0001 | g0011 | AFR | ESN | MFAP5_chr12_8640943_8667826 | MFAP5 | chr12 | 8640943 | 8667826 |
| HG03540 | hp1 | a0001 | c0001 | t0001 | g0147 | AFR | GWD | MFAP5_chr12_8640943_8667826 | MFAP5 | chr12 | 8640943 | 8667826 |
| HG03540 | hp2 | a0001 | c0001 | t0001 | g0016 | AFR | GWD | MFAP5_chr12_8640943_8667826 | MFAP5 | chr12 | 8640943 | 8667826 |
| HG03579 | hp1 | a0001 | c0001 | t0001 | g0091 | AFR | MSL | MFAP5_chr12_8640943_8667826 | MFAP5 | chr12 | 8640943 | 8667826 |
| HG03579 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | MSL | MFAP5_chr12_8640943_8667826 | MFAP5 | chr12 | 8640943 | 8667826 |
| HG03654 | hp1 | a0001 | c0001 | t0001 | g0122 | SAS | PJL | MFAP5_chr12_8640943_8667826 | MFAP5 | chr12 | 8640943 | 8667826 |
| HG03654 | hp2 | a0001 | c0001 | t0001 | g0124 | SAS | PJL | MFAP5_chr12_8640943_8667826 | MFAP5 | chr12 | 8640943 | 8667826 |
| HG03688 | hp1 | a0001 | c0001 | t0001 | g0088 | SAS | STU | MFAP5_chr12_8640943_8667826 | MFAP5 | chr12 | 8640943 | 8667826 |
| HG03688 | hp2 | a0001 | c0001 | t0001 | g0024 | SAS | STU | MFAP5_chr12_8640943_8667826 | MFAP5 | chr12 | 8640943 | 8667826 |
| HG03704 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | MFAP5_chr12_8640943_8667826 | MFAP5 | chr12 | 8640943 | 8667826 |
| HG03704 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | MFAP5_chr12_8640943_8667826 | MFAP5 | chr12 | 8640943 | 8667826 |
| HG03710 | hp1 | a0001 | c0001 | t0001 | g0052 | SAS | PJL | MFAP5_chr12_8640943_8667826 | MFAP5 | chr12 | 8640943 | 8667826 |
| HG03710 | hp2 | a0001 | c0001 | t0004 | g0032 | SAS | PJL | MFAP5_chr12_8640943_8667826 | MFAP5 | chr12 | 8640943 | 8667826 |
| HG03831 | hp1 | a0001 | c0001 | t0001 | g0139 | SAS | BEB | MFAP5_chr12_8640943_8667826 | MFAP5 | chr12 | 8640943 | 8667826 |
| HG03831 | hp2 | a0001 | c0001 | t0001 | g0024 | SAS | BEB | MFAP5_chr12_8640943_8667826 | MFAP5 | chr12 | 8640943 | 8667826 |
| HG03834 | hp1 | a0001 | c0001 | t0001 | g0141 | SAS | BEB | MFAP5_chr12_8640943_8667826 | MFAP5 | chr12 | 8640943 | 8667826 |
| HG03834 | hp2 | a0001 | c0001 | t0009 | g0067 | SAS | BEB | MFAP5_chr12_8640943_8667826 | MFAP5 | chr12 | 8640943 | 8667826 |
| HG03927 | hp1 | a0001 | c0001 | t0001 | g0039 | SAS | BEB | MFAP5_chr12_8640943_8667826 | MFAP5 | chr12 | 8640943 | 8667826 |
| HG03927 | hp2 | a0001 | c0001 | t0001 | g0130 | SAS | BEB | MFAP5_chr12_8640943_8667826 | MFAP5 | chr12 | 8640943 | 8667826 |
| HG03942 | hp1 | a0001 | c0001 | t0001 | g0188 | SAS | BEB | MFAP5_chr12_8640943_8667826 | MFAP5 | chr12 | 8640943 | 8667826 |
| HG03942 | hp2 | a0001 | c0001 | t0001 | g0109 | SAS | BEB | MFAP5_chr12_8640943_8667826 | MFAP5 | chr12 | 8640943 | 8667826 |
| HG04115 | hp1 | a0001 | c0001 | t0005 | g0043 | SAS | STU | MFAP5_chr12_8640943_8667826 | MFAP5 | chr12 | 8640943 | 8667826 |
| HG04115 | hp2 | a0001 | c0001 | t0001 | g0162 | SAS | STU | MFAP5_chr12_8640943_8667826 | MFAP5 | chr12 | 8640943 | 8667826 |
| HG04184 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | BEB | MFAP5_chr12_8640943_8667826 | MFAP5 | chr12 | 8640943 | 8667826 |
| HG04184 | hp2 | a0001 | c0001 | t0001 | g0126 | SAS | BEB | MFAP5_chr12_8640943_8667826 | MFAP5 | chr12 | 8640943 | 8667826 |
| HG04204 | hp1 | a0001 | c0001 | t0018 | g0207 | SAS | STU | MFAP5_chr12_8640943_8667826 | MFAP5 | chr12 | 8640943 | 8667826 |
| HG04204 | hp2 | a0001 | c0001 | t0001 | g0080 | SAS | STU | MFAP5_chr12_8640943_8667826 | MFAP5 | chr12 | 8640943 | 8667826 |
| HG04228 | hp1 | a0001 | c0001 | t0001 | g0044 | SAS | STU | MFAP5_chr12_8640943_8667826 | MFAP5 | chr12 | 8640943 | 8667826 |
| HG04228 | hp2 | a0001 | c0001 | t0001 | g0047 | SAS | STU | MFAP5_chr12_8640943_8667826 | MFAP5 | chr12 | 8640943 | 8667826 |
| NA18522 | hp1 | a0001 | c0001 | t0001 | g0112 | AFR | YRI | MFAP5_chr12_8640943_8667826 | MFAP5 | chr12 | 8640943 | 8667826 |
| NA18522 | hp2 | a0001 | c0001 | t0001 | g0149 | AFR | YRI | MFAP5_chr12_8640943_8667826 | MFAP5 | chr12 | 8640943 | 8667826 |
| NA18747 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CHB | MFAP5_chr12_8640943_8667826 | MFAP5 | chr12 | 8640943 | 8667826 |
| NA18747 | hp2 | a0001 | c0001 | t0001 | g0191 | EAS | CHB | MFAP5_chr12_8640943_8667826 | MFAP5 | chr12 | 8640943 | 8667826 |
| NA18906 | hp1 | a0001 | c0001 | t0010 | g0042 | AFR | YRI | MFAP5_chr12_8640943_8667826 | MFAP5 | chr12 | 8640943 | 8667826 |
| NA18906 | hp2 | a0001 | c0001 | t0001 | g0011 | AFR | YRI | MFAP5_chr12_8640943_8667826 | MFAP5 | chr12 | 8640943 | 8667826 |
| NA18939 | hp1 | a0001 | c0001 | t0001 | g0020 | EAS | JPT | MFAP5_chr12_8640943_8667826 | MFAP5 | chr12 | 8640943 | 8667826 |
| NA18939 | hp2 | a0001 | c0001 | t0001 | g0181 | EAS | JPT | MFAP5_chr12_8640943_8667826 | MFAP5 | chr12 | 8640943 | 8667826 |
| NA18940 | hp1 | a0001 | c0001 | t0001 | g0178 | EAS | JPT | MFAP5_chr12_8640943_8667826 | MFAP5 | chr12 | 8640943 | 8667826 |
| NA18940 | hp2 | a0001 | c0001 | t0001 | g0025 | EAS | JPT | MFAP5_chr12_8640943_8667826 | MFAP5 | chr12 | 8640943 | 8667826 |
| NA18941 | hp1 | a0001 | c0001 | t0001 | g0183 | EAS | JPT | MFAP5_chr12_8640943_8667826 | MFAP5 | chr12 | 8640943 | 8667826 |
| NA18941 | hp2 | a0001 | c0001 | t0001 | g0180 | EAS | JPT | MFAP5_chr12_8640943_8667826 | MFAP5 | chr12 | 8640943 | 8667826 |
| NA18942 | hp1 | a0001 | c0001 | t0001 | g0020 | EAS | JPT | MFAP5_chr12_8640943_8667826 | MFAP5 | chr12 | 8640943 | 8667826 |
| NA18942 | hp2 | a0001 | c0001 | t0001 | g0030 | EAS | JPT | MFAP5_chr12_8640943_8667826 | MFAP5 | chr12 | 8640943 | 8667826 |
| NA18943 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | MFAP5_chr12_8640943_8667826 | MFAP5 | chr12 | 8640943 | 8667826 |
| NA18943 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | MFAP5_chr12_8640943_8667826 | MFAP5 | chr12 | 8640943 | 8667826 |
| NA18944 | hp1 | a0001 | c0001 | t0009 | g0066 | EAS | JPT | MFAP5_chr12_8640943_8667826 | MFAP5 | chr12 | 8640943 | 8667826 |
| NA18944 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | MFAP5_chr12_8640943_8667826 | MFAP5 | chr12 | 8640943 | 8667826 |
| NA18945 | hp1 | a0001 | c0001 | t0001 | g0121 | EAS | JPT | MFAP5_chr12_8640943_8667826 | MFAP5 | chr12 | 8640943 | 8667826 |
| NA18945 | hp2 | a0001 | c0001 | t0001 | g0044 | EAS | JPT | MFAP5_chr12_8640943_8667826 | MFAP5 | chr12 | 8640943 | 8667826 |
| NA18946 | hp1 | a0001 | c0001 | t0001 | g0037 | EAS | JPT | MFAP5_chr12_8640943_8667826 | MFAP5 | chr12 | 8640943 | 8667826 |
| NA18946 | hp2 | a0001 | c0001 | t0013 | g0069 | EAS | JPT | MFAP5_chr12_8640943_8667826 | MFAP5 | chr12 | 8640943 | 8667826 |
| NA18948 | hp1 | a0001 | c0001 | t0001 | g0184 | EAS | JPT | MFAP5_chr12_8640943_8667826 | MFAP5 | chr12 | 8640943 | 8667826 |
| NA18948 | hp2 | a0001 | c0001 | t0001 | g0075 | EAS | JPT | MFAP5_chr12_8640943_8667826 | MFAP5 | chr12 | 8640943 | 8667826 |
| NA18950 | hp1 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | MFAP5_chr12_8640943_8667826 | MFAP5 | chr12 | 8640943 | 8667826 |
| NA18950 | hp2 | a0001 | c0001 | t0001 | g0019 | EAS | JPT | MFAP5_chr12_8640943_8667826 | MFAP5 | chr12 | 8640943 | 8667826 |
| NA18954 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | MFAP5_chr12_8640943_8667826 | MFAP5 | chr12 | 8640943 | 8667826 |
| NA18954 | hp2 | a0001 | c0001 | t0001 | g0082 | EAS | JPT | MFAP5_chr12_8640943_8667826 | MFAP5 | chr12 | 8640943 | 8667826 |
| NA18962 | hp1 | a0001 | c0001 | t0001 | g0131 | EAS | JPT | MFAP5_chr12_8640943_8667826 | MFAP5 | chr12 | 8640943 | 8667826 |
| NA18962 | hp2 | a0001 | c0001 | t0001 | g0142 | EAS | JPT | MFAP5_chr12_8640943_8667826 | MFAP5 | chr12 | 8640943 | 8667826 |
| NA18964 | hp1 | a0001 | c0001 | t0001 | g0150 | EAS | JPT | MFAP5_chr12_8640943_8667826 | MFAP5 | chr12 | 8640943 | 8667826 |
| NA18964 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | MFAP5_chr12_8640943_8667826 | MFAP5 | chr12 | 8640943 | 8667826 |
| NA18965 | hp1 | a0001 | c0001 | t0009 | g0068 | EAS | JPT | MFAP5_chr12_8640943_8667826 | MFAP5 | chr12 | 8640943 | 8667826 |
| NA18965 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | MFAP5_chr12_8640943_8667826 | MFAP5 | chr12 | 8640943 | 8667826 |
| NA18968 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | MFAP5_chr12_8640943_8667826 | MFAP5 | chr12 | 8640943 | 8667826 |
| NA18968 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | MFAP5_chr12_8640943_8667826 | MFAP5 | chr12 | 8640943 | 8667826 |
| NA18970 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | MFAP5_chr12_8640943_8667826 | MFAP5 | chr12 | 8640943 | 8667826 |
| NA18970 | hp2 | a0001 | c0001 | t0001 | g0189 | EAS | JPT | MFAP5_chr12_8640943_8667826 | MFAP5 | chr12 | 8640943 | 8667826 |
| NA18971 | hp1 | a0001 | c0001 | t0005 | g0010 | EAS | JPT | MFAP5_chr12_8640943_8667826 | MFAP5 | chr12 | 8640943 | 8667826 |
| NA18971 | hp2 | a0001 | c0001 | t0001 | g0036 | EAS | JPT | MFAP5_chr12_8640943_8667826 | MFAP5 | chr12 | 8640943 | 8667826 |
| NA18972 | hp1 | a0001 | c0001 | t0001 | g0187 | EAS | JPT | MFAP5_chr12_8640943_8667826 | MFAP5 | chr12 | 8640943 | 8667826 |
| NA18972 | hp2 | a0001 | c0001 | t0001 | g0177 | EAS | JPT | MFAP5_chr12_8640943_8667826 | MFAP5 | chr12 | 8640943 | 8667826 |
| NA18979 | hp1 | a0001 | c0001 | t0001 | g0031 | EAS | JPT | MFAP5_chr12_8640943_8667826 | MFAP5 | chr12 | 8640943 | 8667826 |
| NA18979 | hp2 | a0001 | c0001 | t0001 | g0020 | EAS | JPT | MFAP5_chr12_8640943_8667826 | MFAP5 | chr12 | 8640943 | 8667826 |
| NA18980 | hp1 | a0001 | c0001 | t0001 | g0071 | EAS | JPT | MFAP5_chr12_8640943_8667826 | MFAP5 | chr12 | 8640943 | 8667826 |
| NA18980 | hp2 | a0001 | c0001 | t0001 | g0019 | EAS | JPT | MFAP5_chr12_8640943_8667826 | MFAP5 | chr12 | 8640943 | 8667826 |
| NA18982 | hp1 | a0001 | c0001 | t0001 | g0037 | EAS | JPT | MFAP5_chr12_8640943_8667826 | MFAP5 | chr12 | 8640943 | 8667826 |
| NA18982 | hp2 | a0001 | c0001 | t0001 | g0165 | EAS | JPT | MFAP5_chr12_8640943_8667826 | MFAP5 | chr12 | 8640943 | 8667826 |
| NA18983 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | MFAP5_chr12_8640943_8667826 | MFAP5 | chr12 | 8640943 | 8667826 |
| NA18983 | hp2 | a0001 | c0001 | t0001 | g0030 | EAS | JPT | MFAP5_chr12_8640943_8667826 | MFAP5 | chr12 | 8640943 | 8667826 |
| NA18984 | hp1 | a0001 | c0001 | t0001 | g0026 | EAS | JPT | MFAP5_chr12_8640943_8667826 | MFAP5 | chr12 | 8640943 | 8667826 |
| NA18984 | hp2 | a0001 | c0001 | t0001 | g0049 | EAS | JPT | MFAP5_chr12_8640943_8667826 | MFAP5 | chr12 | 8640943 | 8667826 |
| NA18986 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | MFAP5_chr12_8640943_8667826 | MFAP5 | chr12 | 8640943 | 8667826 |
| NA18986 | hp2 | a0001 | c0001 | t0001 | g0098 | EAS | JPT | MFAP5_chr12_8640943_8667826 | MFAP5 | chr12 | 8640943 | 8667826 |
| NA18989 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | MFAP5_chr12_8640943_8667826 | MFAP5 | chr12 | 8640943 | 8667826 |
| NA18989 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | MFAP5_chr12_8640943_8667826 | MFAP5 | chr12 | 8640943 | 8667826 |
| NA18990 | hp1 | a0001 | c0001 | t0001 | g0145 | EAS | JPT | MFAP5_chr12_8640943_8667826 | MFAP5 | chr12 | 8640943 | 8667826 |
| NA18990 | hp2 | a0001 | c0001 | t0001 | g0190 | EAS | JPT | MFAP5_chr12_8640943_8667826 | MFAP5 | chr12 | 8640943 | 8667826 |
| NA18994 | hp1 | a0001 | c0001 | t0001 | g0045 | EAS | JPT | MFAP5_chr12_8640943_8667826 | MFAP5 | chr12 | 8640943 | 8667826 |
| NA18994 | hp2 | a0001 | c0001 | t0001 | g0137 | EAS | JPT | MFAP5_chr12_8640943_8667826 | MFAP5 | chr12 | 8640943 | 8667826 |
| NA18997 | hp1 | a0001 | c0001 | t0001 | g0155 | EAS | JPT | MFAP5_chr12_8640943_8667826 | MFAP5 | chr12 | 8640943 | 8667826 |
| NA18997 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | MFAP5_chr12_8640943_8667826 | MFAP5 | chr12 | 8640943 | 8667826 |
| NA18998 | hp1 | a0001 | c0001 | t0001 | g0026 | EAS | JPT | MFAP5_chr12_8640943_8667826 | MFAP5 | chr12 | 8640943 | 8667826 |
| NA18998 | hp2 | a0001 | c0001 | t0001 | g0134 | EAS | JPT | MFAP5_chr12_8640943_8667826 | MFAP5 | chr12 | 8640943 | 8667826 |
| NA19001 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | MFAP5_chr12_8640943_8667826 | MFAP5 | chr12 | 8640943 | 8667826 |
| NA19001 | hp2 | a0001 | c0001 | t0001 | g0054 | EAS | JPT | MFAP5_chr12_8640943_8667826 | MFAP5 | chr12 | 8640943 | 8667826 |
| NA19002 | hp1 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | MFAP5_chr12_8640943_8667826 | MFAP5 | chr12 | 8640943 | 8667826 |
| NA19002 | hp2 | a0001 | c0001 | t0001 | g0195 | EAS | JPT | MFAP5_chr12_8640943_8667826 | MFAP5 | chr12 | 8640943 | 8667826 |
| NA19003 | hp1 | a0001 | c0001 | t0001 | g0179 | EAS | JPT | MFAP5_chr12_8640943_8667826 | MFAP5 | chr12 | 8640943 | 8667826 |
| NA19003 | hp2 | a0001 | c0001 | t0001 | g0078 | EAS | JPT | MFAP5_chr12_8640943_8667826 | MFAP5 | chr12 | 8640943 | 8667826 |
| NA19004 | hp1 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | MFAP5_chr12_8640943_8667826 | MFAP5 | chr12 | 8640943 | 8667826 |
| NA19004 | hp2 | a0001 | c0001 | t0001 | g0024 | EAS | JPT | MFAP5_chr12_8640943_8667826 | MFAP5 | chr12 | 8640943 | 8667826 |
| NA19005 | hp1 | a0001 | c0001 | t0001 | g0036 | EAS | JPT | MFAP5_chr12_8640943_8667826 | MFAP5 | chr12 | 8640943 | 8667826 |
| NA19005 | hp2 | a0001 | c0001 | t0001 | g0077 | EAS | JPT | MFAP5_chr12_8640943_8667826 | MFAP5 | chr12 | 8640943 | 8667826 |
| NA19007 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | MFAP5_chr12_8640943_8667826 | MFAP5 | chr12 | 8640943 | 8667826 |
| NA19007 | hp2 | a0001 | c0001 | t0001 | g0023 | EAS | JPT | MFAP5_chr12_8640943_8667826 | MFAP5 | chr12 | 8640943 | 8667826 |
| NA19011 | hp1 | a0001 | c0001 | t0001 | g0166 | EAS | JPT | MFAP5_chr12_8640943_8667826 | MFAP5 | chr12 | 8640943 | 8667826 |
| NA19011 | hp2 | a0001 | c0001 | t0001 | g0164 | EAS | JPT | MFAP5_chr12_8640943_8667826 | MFAP5 | chr12 | 8640943 | 8667826 |
| NA19012 | hp1 | a0001 | c0001 | t0001 | g0123 | EAS | JPT | MFAP5_chr12_8640943_8667826 | MFAP5 | chr12 | 8640943 | 8667826 |
| NA19012 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | MFAP5_chr12_8640943_8667826 | MFAP5 | chr12 | 8640943 | 8667826 |
| NA19030 | hp1 | a0001 | c0001 | t0003 | g0199 | AFR | LWK | MFAP5_chr12_8640943_8667826 | MFAP5 | chr12 | 8640943 | 8667826 |
| NA19030 | hp2 | a0001 | c0001 | t0001 | g0012 | AFR | LWK | MFAP5_chr12_8640943_8667826 | MFAP5 | chr12 | 8640943 | 8667826 |
| NA19043 | hp1 | a0001 | c0001 | t0001 | g0158 | AFR | LWK | MFAP5_chr12_8640943_8667826 | MFAP5 | chr12 | 8640943 | 8667826 |
| NA19043 | hp2 | a0001 | c0001 | t0001 | g0002 | AFR | LWK | MFAP5_chr12_8640943_8667826 | MFAP5 | chr12 | 8640943 | 8667826 |
| NA19058 | hp1 | a0001 | c0001 | t0001 | g0017 | EAS | JPT | MFAP5_chr12_8640943_8667826 | MFAP5 | chr12 | 8640943 | 8667826 |
| NA19058 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | MFAP5_chr12_8640943_8667826 | MFAP5 | chr12 | 8640943 | 8667826 |
| NA19062 | hp1 | a0001 | c0001 | t0001 | g0015 | EAS | JPT | MFAP5_chr12_8640943_8667826 | MFAP5 | chr12 | 8640943 | 8667826 |
| NA19062 | hp2 | a0001 | c0001 | t0001 | g0143 | EAS | JPT | MFAP5_chr12_8640943_8667826 | MFAP5 | chr12 | 8640943 | 8667826 |
| NA19065 | hp1 | a0001 | c0001 | t0001 | g0023 | EAS | JPT | MFAP5_chr12_8640943_8667826 | MFAP5 | chr12 | 8640943 | 8667826 |
| NA19065 | hp2 | a0001 | c0001 | t0001 | g0079 | EAS | JPT | MFAP5_chr12_8640943_8667826 | MFAP5 | chr12 | 8640943 | 8667826 |
| NA19067 | hp1 | a0001 | c0001 | t0001 | g0116 | EAS | JPT | MFAP5_chr12_8640943_8667826 | MFAP5 | chr12 | 8640943 | 8667826 |
| NA19067 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | MFAP5_chr12_8640943_8667826 | MFAP5 | chr12 | 8640943 | 8667826 |
| NA19070 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | MFAP5_chr12_8640943_8667826 | MFAP5 | chr12 | 8640943 | 8667826 |
| NA19070 | hp2 | a0001 | c0001 | t0001 | g0019 | EAS | JPT | MFAP5_chr12_8640943_8667826 | MFAP5 | chr12 | 8640943 | 8667826 |
| NA19072 | hp1 | a0001 | c0001 | t0001 | g0182 | EAS | JPT | MFAP5_chr12_8640943_8667826 | MFAP5 | chr12 | 8640943 | 8667826 |
| NA19072 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | MFAP5_chr12_8640943_8667826 | MFAP5 | chr12 | 8640943 | 8667826 |
| NA19074 | hp1 | a0001 | c0001 | t0001 | g0185 | EAS | JPT | MFAP5_chr12_8640943_8667826 | MFAP5 | chr12 | 8640943 | 8667826 |
| NA19074 | hp2 | a0001 | c0001 | t0014 | g0156 | EAS | JPT | MFAP5_chr12_8640943_8667826 | MFAP5 | chr12 | 8640943 | 8667826 |
| NA19077 | hp1 | a0001 | c0001 | t0001 | g0023 | EAS | JPT | MFAP5_chr12_8640943_8667826 | MFAP5 | chr12 | 8640943 | 8667826 |
| NA19077 | hp2 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | MFAP5_chr12_8640943_8667826 | MFAP5 | chr12 | 8640943 | 8667826 |
| NA19078 | hp1 | a0001 | c0001 | t0001 | g0048 | EAS | JPT | MFAP5_chr12_8640943_8667826 | MFAP5 | chr12 | 8640943 | 8667826 |
| NA19078 | hp2 | a0001 | c0001 | t0001 | g0048 | EAS | JPT | MFAP5_chr12_8640943_8667826 | MFAP5 | chr12 | 8640943 | 8667826 |
| NA19079 | hp1 | a0001 | c0001 | t0001 | g0095 | EAS | JPT | MFAP5_chr12_8640943_8667826 | MFAP5 | chr12 | 8640943 | 8667826 |
| NA19079 | hp2 | a0001 | c0001 | t0001 | g0049 | EAS | JPT | MFAP5_chr12_8640943_8667826 | MFAP5 | chr12 | 8640943 | 8667826 |
| NA19081 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | MFAP5_chr12_8640943_8667826 | MFAP5 | chr12 | 8640943 | 8667826 |
| NA19081 | hp2 | a0001 | c0001 | t0001 | g0186 | EAS | JPT | MFAP5_chr12_8640943_8667826 | MFAP5 | chr12 | 8640943 | 8667826 |
| NA19082 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | MFAP5_chr12_8640943_8667826 | MFAP5 | chr12 | 8640943 | 8667826 |
| NA19082 | hp2 | a0001 | c0001 | t0001 | g0120 | EAS | JPT | MFAP5_chr12_8640943_8667826 | MFAP5 | chr12 | 8640943 | 8667826 |
| NA19085 | hp1 | a0001 | c0001 | t0001 | g0096 | EAS | JPT | MFAP5_chr12_8640943_8667826 | MFAP5 | chr12 | 8640943 | 8667826 |
| NA19085 | hp2 | a0001 | c0001 | t0015 | g0128 | EAS | JPT | MFAP5_chr12_8640943_8667826 | MFAP5 | chr12 | 8640943 | 8667826 |
| NA19088 | hp1 | a0001 | c0001 | t0001 | g0015 | EAS | JPT | MFAP5_chr12_8640943_8667826 | MFAP5 | chr12 | 8640943 | 8667826 |
| NA19088 | hp2 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | MFAP5_chr12_8640943_8667826 | MFAP5 | chr12 | 8640943 | 8667826 |
| NA19089 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | MFAP5_chr12_8640943_8667826 | MFAP5 | chr12 | 8640943 | 8667826 |
| NA19089 | hp2 | a0001 | c0001 | t0001 | g0117 | EAS | JPT | MFAP5_chr12_8640943_8667826 | MFAP5 | chr12 | 8640943 | 8667826 |
| NA19090 | hp1 | a0001 | c0001 | t0001 | g0074 | EAS | JPT | MFAP5_chr12_8640943_8667826 | MFAP5 | chr12 | 8640943 | 8667826 |
| NA19090 | hp2 | a0001 | c0001 | t0001 | g0017 | EAS | JPT | MFAP5_chr12_8640943_8667826 | MFAP5 | chr12 | 8640943 | 8667826 |
| NA19240 | hp1 | a0001 | c0001 | t0006 | g0173 | AFR | YRI | MFAP5_chr12_8640943_8667826 | MFAP5 | chr12 | 8640943 | 8667826 |
| NA19240 | hp2 | a0001 | c0001 | t0002 | g0176 | AFR | YRI | MFAP5_chr12_8640943_8667826 | MFAP5 | chr12 | 8640943 | 8667826 |
| NA20129 | hp1 | a0001 | c0001 | t0001 | g0007 | AFR | ASW | MFAP5_chr12_8640943_8667826 | MFAP5 | chr12 | 8640943 | 8667826 |
| NA20129 | hp2 | a0001 | c0001 | t0001 | g0097 | AFR | ASW | MFAP5_chr12_8640943_8667826 | MFAP5 | chr12 | 8640943 | 8667826 |
| NA20752 | hp1 | a0001 | c0001 | t0001 | g0002 | EUR | TSI | MFAP5_chr12_8640943_8667826 | MFAP5 | chr12 | 8640943 | 8667826 |
| NA20752 | hp2 | a0001 | c0001 | t0004 | g0032 | EUR | TSI | MFAP5_chr12_8640943_8667826 | MFAP5 | chr12 | 8640943 | 8667826 |
| NA20905 | hp1 | a0001 | c0001 | t0001 | g0094 | SAS | GIH | MFAP5_chr12_8640943_8667826 | MFAP5 | chr12 | 8640943 | 8667826 |
| NA20905 | hp2 | a0001 | c0001 | t0005 | g0043 | SAS | GIH | MFAP5_chr12_8640943_8667826 | MFAP5 | chr12 | 8640943 | 8667826 |
| HG01123 | hp1 | a0001 | c0001 | t0004 | g0018 | AMR | CLM | MFAP5_chr12_8640943_8667826 | MFAP5 | chr12 | 8640943 | 8667826 |
| HG01123 | hp2 | a0001 | c0001 | t0002 | g0100 | AMR | CLM | MFAP5_chr12_8640943_8667826 | MFAP5 | chr12 | 8640943 | 8667826 |
| HG02109 | hp1 | a0001 | c0001 | t0003 | g0057 | AFR | ACB | MFAP5_chr12_8640943_8667826 | MFAP5 | chr12 | 8640943 | 8667826 |
| HG02109 | hp2 | a0001 | c0001 | t0005 | g0053 | AFR | ACB | MFAP5_chr12_8640943_8667826 | MFAP5 | chr12 | 8640943 | 8667826 |
| HG02486 | hp1 | a0001 | c0001 | t0001 | g0168 | AFR | ACB | MFAP5_chr12_8640943_8667826 | MFAP5 | chr12 | 8640943 | 8667826 |
| HG02486 | hp2 | a0001 | c0001 | t0001 | g0055 | AFR | ACB | MFAP5_chr12_8640943_8667826 | MFAP5 | chr12 | 8640943 | 8667826 |
| HG02559 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | ACB | MFAP5_chr12_8640943_8667826 | MFAP5 | chr12 | 8640943 | 8667826 |
| HG02559 | hp2 | a0001 | c0001 | t0001 | g0114 | AFR | ACB | MFAP5_chr12_8640943_8667826 | MFAP5 | chr12 | 8640943 | 8667826 |
| HG03471 | hp1 | a0001 | c0001 | t0001 | g0028 | AFR | MSL | MFAP5_chr12_8640943_8667826 | MFAP5 | chr12 | 8640943 | 8667826 |
| HG03471 | hp2 | a0001 | c0001 | t0001 | g0103 | AFR | MSL | MFAP5_chr12_8640943_8667826 | MFAP5 | chr12 | 8640943 | 8667826 |
| HG06807 | hp1 | a0001 | c0001 | t0011 | g0148 | AFR | USA | MFAP5_chr12_8640943_8667826 | MFAP5 | chr12 | 8640943 | 8667826 |
| HG06807 | hp2 | a0001 | c0001 | t0002 | g0003 | AFR | USA | MFAP5_chr12_8640943_8667826 | MFAP5 | chr12 | 8640943 | 8667826 |
| NA18955 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | MFAP5_chr12_8640943_8667826 | MFAP5 | chr12 | 8640943 | 8667826 |
| NA18955 | hp2 | a0001 | c0001 | t0001 | g0136 | EAS | JPT | MFAP5_chr12_8640943_8667826 | MFAP5 | chr12 | 8640943 | 8667826 |
| NA20300 | hp1 | a0001 | c0001 | t0001 | g0138 | AFR | USA | MFAP5_chr12_8640943_8667826 | MFAP5 | chr12 | 8640943 | 8667826 |
| NA20300 | hp2 | a0001 | c0001 | t0001 | g0013 | AFR | USA | MFAP5_chr12_8640943_8667826 | MFAP5 | chr12 | 8640943 | 8667826 |
| NA21309 | hp1 | a0001 | c0001 | t0001 | g0159 | AFR | LWK | MFAP5_chr12_8640943_8667826 | MFAP5 | chr12 | 8640943 | 8667826 |
| NA21309 | hp2 | a0001 | c0001 | t0001 | g0106 | AFR | LWK | MFAP5_chr12_8640943_8667826 | MFAP5 | chr12 | 8640943 | 8667826 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0004 | g0061 | REF | REF | MFAP5_chr12_8640943_8667826 | MFAP5 | chr12 | 8640943 | 8667826 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0001 | g0007 | REF | REF | MFAP5_chr12_8640943_8667826 | MFAP5 | chr12 | 8640943 | 8667826 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr12:8649542 | A | G | 1 | a0002 | 1 | HG02056.hp1 | missense_variant | MODERATE | c.368T>C | p.Ile123Thr | MFAP5 | ENSG00000197614.11 | transcript | ENST00000359478.7 | protein_coding | 9/10 | 570/2872 | 368/522 | 123/173 | chr12 | 8649542 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr12:8649517 | T | C | 1 | a0001c0003 | 1 | HG02970.hp1 | synonymous_variant | LOW | c.393A>G | p.Glu131Glu | MFAP5 | ENSG00000197614.11 | transcript | ENST00000359478.7 | protein_coding | 9/10 | 595/2872 | 393/522 | 131/173 | chr12 | 8649517 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr12:8645982 | GA | G | 1 | a0001c0001t0007 | 5 | HG00738.hp1 HG01071.hp1 HG01256.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*2108delT | MFAP5 | ENSG00000197614.11 | transcript | ENST00000359478.7 | protein_coding | 10/10 | 2108 | chr12 | 8645982 | ||||||
| chr12:8646239 | A | AT | 2 | a0001c0001t0009 a0001c0001t0015 |
4 | HG03834.hp2 NA18944.hp1 NA18965.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*1851dupA | MFAP5 | ENSG00000197614.11 | transcript | ENST00000359478.7 | protein_coding | 10/10 | 1851 | chr12 | 8646239 | ||||||
| chr12:8646275 | G | T | 5 | a0001c0001t0004 a0001c0001t0005 a0001c0001t0009 others(2): Show |
25 | HG00280.hp1 HG00323.hp2 HG00408.hp1 others(22): Show |
3_prime_UTR_variant | MODIFIER | c.*1816C>A | MFAP5 | ENSG00000197614.11 | transcript | ENST00000359478.7 | protein_coding | 10/10 | 1816 | chr12 | 8646275 | ||||||
| chr12:8646521 | G | C | 2 | a0001c0001t0009 a0001c0001t0015 |
4 | HG03834.hp2 NA18944.hp1 NA18965.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*1570C>G | MFAP5 | ENSG00000197614.11 | transcript | ENST00000359478.7 | protein_coding | 10/10 | 1570 | chr12 | 8646521 | ||||||
| chr12:8646540 | A | G | 1 | a0001c0001t0017 | 1 | HG03098.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1551T>C | MFAP5 | ENSG00000197614.11 | transcript | ENST00000359478.7 | protein_coding | 10/10 | 1551 | chr12 | 8646540 | ||||||
| chr12:8646562 | A | T | 2 | a0001c0001t0009 a0001c0001t0015 |
4 | HG03834.hp2 NA18944.hp1 NA18965.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*1529T>A | MFAP5 | ENSG00000197614.11 | transcript | ENST00000359478.7 | protein_coding | 10/10 | 1529 | chr12 | 8646562 | ||||||
| chr12:8646904 | A | G | 7 | a0001c0001t0003 a0001c0001t0004 a0001c0001t0005 others(4): Show |
43 | HG00280.hp1 HG00323.hp2 HG00408.hp1 others(40): Show |
3_prime_UTR_variant | MODIFIER | c.*1187T>C | MFAP5 | ENSG00000197614.11 | transcript | ENST00000359478.7 | protein_coding | 10/10 | 1187 | chr12 | 8646904 | ||||||
| chr12:8647076 | T | C | 2 | a0001c0001t0004 a0001c0001t0005 |
20 | HG00280.hp1 HG00323.hp2 HG00408.hp1 others(17): Show |
3_prime_UTR_variant | MODIFIER | c.*1015A>G | MFAP5 | ENSG00000197614.11 | transcript | ENST00000359478.7 | protein_coding | 10/10 | 1015 | chr12 | 8647076 | ||||||
| chr12:8647310 | G | A | 7 | a0001c0001t0003 a0001c0001t0004 a0001c0001t0005 others(4): Show |
43 | HG00280.hp1 HG00323.hp2 HG00408.hp1 others(40): Show |
3_prime_UTR_variant | MODIFIER | c.*781C>T | MFAP5 | ENSG00000197614.11 | transcript | ENST00000359478.7 | protein_coding | 10/10 | 781 | chr12 | 8647310 | ||||||
| chr12:8647447 | A | G | 1 | a0001c0001t0011 | 2 | HG03516.hp1 HG06807.hp1 |
3_prime_UTR_variant | MODIFIER | c.*644T>C | MFAP5 | ENSG00000197614.11 | transcript | ENST00000359478.7 | protein_coding | 10/10 | 644 | chr12 | 8647447 | ||||||
| chr12:8647644 | T | C | 1 | a0001c0001t0017 | 1 | HG03098.hp1 | 3_prime_UTR_variant | MODIFIER | c.*447A>G | MFAP5 | ENSG00000197614.11 | transcript | ENST00000359478.7 | protein_coding | 10/10 | 447 | chr12 | 8647644 | ||||||
| chr12:8647714 | G | T | 1 | a0001c0001t0010 | 2 | HG02976.hp2 NA18906.hp1 |
3_prime_UTR_variant | MODIFIER | c.*377C>A | MFAP5 | ENSG00000197614.11 | transcript | ENST00000359478.7 | protein_coding | 10/10 | 377 | chr12 | 8647714 | ||||||
| chr12:8647803 | T | C | 1 | a0001c0001t0016 | 1 | HG00280.hp2 | 3_prime_UTR_variant | MODIFIER | c.*288A>G | MFAP5 | ENSG00000197614.11 | transcript | ENST00000359478.7 | protein_coding | 10/10 | 288 | chr12 | 8647803 | ||||||
| chr12:8647823 | C | T | 1 | a0001c0001t0017 | 1 | HG03098.hp1 | 3_prime_UTR_variant | MODIFIER | c.*268G>A | MFAP5 | ENSG00000197614.11 | transcript | ENST00000359478.7 | protein_coding | 10/10 | 268 | chr12 | 8647823 | ||||||
| chr12:8647970 | A | G | 1 | a0001c0001t0002 | 19 | HG00099.hp1 HG00140.hp2 HG00639.hp1 others(16): Show |
3_prime_UTR_variant | MODIFIER | c.*121T>C | MFAP5 | ENSG00000197614.11 | transcript | ENST00000359478.7 | protein_coding | 10/10 | 121 | chr12 | 8647970 | ||||||
| chr12:8647977 | A | G | 1 | a0001c0001t0014 | 1 | NA19074.hp2 | 3_prime_UTR_variant | MODIFIER | c.*114T>C | MFAP5 | ENSG00000197614.11 | transcript | ENST00000359478.7 | protein_coding | 10/10 | 114 | chr12 | 8647977 | ||||||
| chr12:8662689 | T | TA | 4 | a0001c0001t0003 a0001c0001t0012 a0001c0001t0017 others(1): Show |
15 | HG01168.hp2 HG01169.hp1 HG01261.hp1 others(12): Show |
5_prime_UTR_variant | MODIFIER | c.-66dupT | MFAP5 | ENSG00000197614.11 | transcript | ENST00000359478.7 | protein_coding | 1/10 | 586 | chr12 | 8662689 | ||||||
| chr12:8662691 | C | T | 2 | a0001c0001t0009 a0001c0001t0013 |
4 | HG03834.hp2 NA18944.hp1 NA18946.hp2 others(1): Show |
5_prime_UTR_variant | MODIFIER | c.-67G>A | MFAP5 | ENSG00000197614.11 | transcript | ENST00000359478.7 | protein_coding | 1/10 | 587 | chr12 | 8662691 | ||||||
| chr12:8662764 | G | A | 1 | a0001c0001t0018 | 1 | HG04204.hp1 | 5_prime_UTR_variant | MODIFIER | c.-140C>T | MFAP5 | ENSG00000197614.11 | transcript | ENST00000359478.7 | protein_coding | 1/10 | 660 | chr12 | 8662764 | ||||||
| chr12:8662802 | C | G | 2 | a0001c0001t0004 a0001c0001t0008 |
14 | HG00280.hp1 HG00323.hp2 HG01123.hp1 others(11): Show |
5_prime_UTR_variant | MODIFIER | c.-178G>C | MFAP5 | ENSG00000197614.11 | transcript | ENST00000359478.7 | protein_coding | 1/10 | 698 | chr12 | 8662802 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr12:8648221 | C | T | 1 | a0001c0001t0017g0204 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.410-18G>A | MFAP5 | ENSG00000197614.11 | transcript | ENST00000359478.7 | protein_coding | 9/9 | chr12 | 8648221 | |||||||
| chr12:8648426 | A | G | 1 | a0001c0001t0001g0145 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.410-223T>C | MFAP5 | ENSG00000197614.11 | transcript | ENST00000359478.7 | protein_coding | 9/9 | chr12 | 8648426 | |||||||
| chr12:8648486 | C | A | 1 | a0001c0001t0002g0051 | 2 | HG00099.hp1 HG00140.hp2 |
intron_variant | MODIFIER | c.410-283G>T | MFAP5 | ENSG00000197614.11 | transcript | ENST00000359478.7 | protein_coding | 9/9 | chr12 | 8648486 | |||||||
| chr12:8648686 | C | T | 2 | a0001c0001t0001g0028 a0001c0001t0001g0147 |
4 | HG01074.hp2 HG03041.hp2 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.410-483G>A | MFAP5 | ENSG00000197614.11 | transcript | ENST00000359478.7 | protein_coding | 9/9 | chr12 | 8648686 | |||||||
| chr12:8648795 | G | A | 3 | a0001c0001t0003g0057 a0001c0001t0003g0206 a0001c0001t0006g0105 |
4 | HG02109.hp1 HG02717.hp1 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.410-592C>T | MFAP5 | ENSG00000197614.11 | transcript | ENST00000359478.7 | protein_coding | 9/9 | chr12 | 8648795 | |||||||
| chr12:8649298 | TTCTTAGG others(14): Show |
T | 1 | a0001c0001t0001g0109 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.409+182_409+202del others(21): Show |
MFAP5 | ENSG00000197614.11 | transcript | ENST00000359478.7 | protein_coding | 9/9 | chr12 | 8649298 | |||||||
| chr12:8649314 | T | TCTTAG | 5 | a0001c0001t0001g0016 a0001c0001t0001g0114 a0001c0001t0001g0151 others(2): Show |
8 | HG01891.hp2 HG02280.hp1 HG02559.hp2 others(5): Show |
intron_variant | MODIFIER | c.409+186_409+187ins others(5): Show |
MFAP5 | ENSG00000197614.11 | transcript | ENST00000359478.7 | protein_coding | 9/9 | chr12 | 8649314 | |||||||
| chr12:8649316 | T | G | 5 | a0001c0001t0001g0016 a0001c0001t0001g0114 a0001c0001t0001g0151 others(2): Show |
8 | HG01891.hp2 HG02280.hp1 HG02559.hp2 others(5): Show |
intron_variant | MODIFIER | c.409+185A>C | MFAP5 | ENSG00000197614.11 | transcript | ENST00000359478.7 | protein_coding | 9/9 | chr12 | 8649316 | |||||||
| chr12:8649317 | A | T | 5 | a0001c0001t0001g0016 a0001c0001t0001g0114 a0001c0001t0001g0151 others(2): Show |
8 | HG01891.hp2 HG02280.hp1 HG02559.hp2 others(5): Show |
intron_variant | MODIFIER | c.409+184T>A | MFAP5 | ENSG00000197614.11 | transcript | ENST00000359478.7 | protein_coding | 9/9 | chr12 | 8649317 | |||||||
| chr12:8649321 | C | A | 5 | a0001c0001t0001g0016 a0001c0001t0001g0114 a0001c0001t0001g0151 others(2): Show |
8 | HG01891.hp2 HG02280.hp1 HG02559.hp2 others(5): Show |
intron_variant | MODIFIER | c.409+180G>T | MFAP5 | ENSG00000197614.11 | transcript | ENST00000359478.7 | protein_coding | 9/9 | chr12 | 8649321 | |||||||
| chr12:8649412 | G | A | 16 | a0001c0001t0004g0018 a0001c0001t0004g0032 a0001c0001t0004g0033 others(13): Show |
26 | HG00280.hp1 HG00323.hp2 HG00408.hp1 others(23): Show |
intron_variant | MODIFIER | c.409+89C>T | MFAP5 | ENSG00000197614.11 | transcript | ENST00000359478.7 | protein_coding | 9/9 | chr12 | 8649412 | |||||||
| chr12:8649583 | G | A | 4 | a0001c0001t0009g0066 a0001c0001t0009g0067 a0001c0001t0009g0068 others(1): Show |
4 | HG03834.hp2 NA18944.hp1 NA18965.hp1 others(1): Show |
intron_variant | MODIFIER | c.336-9C>T | MFAP5 | ENSG00000197614.11 | transcript | ENST00000359478.7 | protein_coding | 8/9 | chr12 | 8649583 | |||||||
| chr12:8649814 | C | T | 1 | a0001c0001t0006g0105 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.336-240G>A | MFAP5 | ENSG00000197614.11 | transcript | ENST00000359478.7 | protein_coding | 8/9 | chr12 | 8649814 | |||||||
| chr12:8649836 | A | G | 24 | a0001c0001t0003g0056 a0001c0001t0003g0196 a0001c0001t0003g0197 others(21): Show |
35 | HG00280.hp1 HG00323.hp2 HG00408.hp1 others(32): Show |
intron_variant | MODIFIER | c.336-262T>C | MFAP5 | ENSG00000197614.11 | transcript | ENST00000359478.7 | protein_coding | 8/9 | chr12 | 8649836 | |||||||
| chr12:8649897 | C | T | 29 | a0001c0001t0003g0056 a0001c0001t0003g0196 a0001c0001t0003g0197 others(26): Show |
40 | HG00280.hp1 HG00323.hp2 HG00408.hp1 others(37): Show |
intron_variant | MODIFIER | c.336-323G>A | MFAP5 | ENSG00000197614.11 | transcript | ENST00000359478.7 | protein_coding | 8/9 | chr12 | 8649897 | |||||||
| chr12:8649905 | A | G | 4 | a0001c0001t0006g0084 a0001c0001t0006g0171 a0001c0001t0006g0172 others(1): Show |
4 | HG01891.hp1 HG02622.hp2 HG02809.hp2 others(1): Show |
intron_variant | MODIFIER | c.336-331T>C | MFAP5 | ENSG00000197614.11 | transcript | ENST00000359478.7 | protein_coding | 8/9 | chr12 | 8649905 | |||||||
| chr12:8649912 | G | A | 1 | a0001c0001t0001g0190 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.336-338C>T | MFAP5 | ENSG00000197614.11 | transcript | ENST00000359478.7 | protein_coding | 8/9 | chr12 | 8649912 | |||||||
| chr12:8650223 | A | G | 1 | a0001c0001t0003g0201 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.335+279T>C | MFAP5 | ENSG00000197614.11 | transcript | ENST00000359478.7 | protein_coding | 8/9 | chr12 | 8650223 | |||||||
| chr12:8650260 | C | T | 11 | a0001c0001t0004g0018 a0001c0001t0004g0032 a0001c0001t0004g0033 others(8): Show |
21 | HG00280.hp1 HG00323.hp2 HG00408.hp1 others(18): Show |
intron_variant | MODIFIER | c.335+242G>A | MFAP5 | ENSG00000197614.11 | transcript | ENST00000359478.7 | protein_coding | 8/9 | chr12 | 8650260 | |||||||
| chr12:8650278 | C | T | 11 | a0001c0001t0004g0018 a0001c0001t0004g0032 a0001c0001t0004g0033 others(8): Show |
21 | HG00280.hp1 HG00323.hp2 HG00408.hp1 others(18): Show |
intron_variant | MODIFIER | c.335+224G>A | MFAP5 | ENSG00000197614.11 | transcript | ENST00000359478.7 | protein_coding | 8/9 | chr12 | 8650278 | |||||||
| chr12:8650311 | T | C | 1 | a0001c0001t0001g0121 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.335+191A>G | MFAP5 | ENSG00000197614.11 | transcript | ENST00000359478.7 | protein_coding | 8/9 | chr12 | 8650311 | |||||||
| chr12:8650366 | C | A | 14 | a0001c0001t0004g0018 a0001c0001t0004g0032 a0001c0001t0004g0033 others(11): Show |
24 | HG00280.hp1 HG00323.hp2 HG00408.hp1 others(21): Show |
intron_variant | MODIFIER | c.335+136G>T | MFAP5 | ENSG00000197614.11 | transcript | ENST00000359478.7 | protein_coding | 8/9 | chr12 | 8650366 | |||||||
| chr12:8650606 | CA | C | 31 | a0001c0001t0003g0056 a0001c0001t0003g0057 a0001c0001t0003g0196 others(28): Show |
43 | HG00280.hp1 HG00323.hp2 HG00408.hp1 others(40): Show |
intron_variant | MODIFIER | c.248-18delT | MFAP5 | ENSG00000197614.11 | transcript | ENST00000359478.7 | protein_coding | 7/9 | chr12 | 8650606 | |||||||
| chr12:8650639 | T | C | 21 | a0001c0001t0003g0056 a0001c0001t0003g0057 a0001c0001t0003g0196 others(18): Show |
23 | HG01168.hp2 HG01169.hp1 HG01261.hp1 others(20): Show |
intron_variant | MODIFIER | c.248-50A>G | MFAP5 | ENSG00000197614.11 | transcript | ENST00000359478.7 | protein_coding | 7/9 | chr12 | 8650639 | |||||||
| chr12:8650729 | A | G | 1 | a0001c0001t0001g0055 | 2 | HG02486.hp2 HG02809.hp1 |
intron_variant | MODIFIER | c.248-140T>C | MFAP5 | ENSG00000197614.11 | transcript | ENST00000359478.7 | protein_coding | 7/9 | chr12 | 8650729 | |||||||
| chr12:8650777 | G | C | 1 | a0001c0001t0001g0101 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.248-188C>G | MFAP5 | ENSG00000197614.11 | transcript | ENST00000359478.7 | protein_coding | 7/9 | chr12 | 8650777 | |||||||
| chr12:8650819 | A | G | 1 | a0001c0001t0001g0087 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.248-230T>C | MFAP5 | ENSG00000197614.11 | transcript | ENST00000359478.7 | protein_coding | 7/9 | chr12 | 8650819 | |||||||
| chr12:8650863 | G | A | 4 | a0001c0001t0009g0066 a0001c0001t0009g0067 a0001c0001t0009g0068 others(1): Show |
4 | HG03834.hp2 NA18944.hp1 NA18965.hp1 others(1): Show |
intron_variant | MODIFIER | c.248-274C>T | MFAP5 | ENSG00000197614.11 | transcript | ENST00000359478.7 | protein_coding | 7/9 | chr12 | 8650863 | |||||||
| chr12:8650949 | C | T | 1 | a0001c0001t0001g0189 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.248-360G>A | MFAP5 | ENSG00000197614.11 | transcript | ENST00000359478.7 | protein_coding | 7/9 | chr12 | 8650949 | |||||||
| chr12:8650965 | G | A | 2 | a0001c0001t0005g0034 a0001c0001t0005g0053 |
4 | HG02109.hp2 HG02723.hp2 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.248-376C>T | MFAP5 | ENSG00000197614.11 | transcript | ENST00000359478.7 | protein_coding | 7/9 | chr12 | 8650965 | |||||||
| chr12:8650995 | C | T | 2 | a0001c0001t0001g0142 a0001c0001t0001g0143 |
2 | NA18962.hp2 NA19062.hp2 |
intron_variant | MODIFIER | c.248-406G>A | MFAP5 | ENSG00000197614.11 | transcript | ENST00000359478.7 | protein_coding | 7/9 | chr12 | 8650995 | |||||||
| chr12:8651001 | T | C | 2 | a0001c0001t0001g0035 a0001c0001t0001g0073 |
3 | HG01192.hp1 HG01243.hp1 HG01256.hp1 |
intron_variant | MODIFIER | c.248-412A>G | MFAP5 | ENSG00000197614.11 | transcript | ENST00000359478.7 | protein_coding | 7/9 | chr12 | 8651001 | |||||||
| chr12:8651051 | C | T | 1 | a0001c0001t0001g0127 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.248-462G>A | MFAP5 | ENSG00000197614.11 | transcript | ENST00000359478.7 | protein_coding | 7/9 | chr12 | 8651051 | |||||||
| chr12:8651092 | G | C | 4 | a0001c0001t0009g0066 a0001c0001t0009g0067 a0001c0001t0009g0068 others(1): Show |
4 | HG03834.hp2 NA18944.hp1 NA18965.hp1 others(1): Show |
intron_variant | MODIFIER | c.248-503C>G | MFAP5 | ENSG00000197614.11 | transcript | ENST00000359478.7 | protein_coding | 7/9 | chr12 | 8651092 | |||||||
| chr12:8651099 | G | T | 4 | a0001c0001t0009g0066 a0001c0001t0009g0067 a0001c0001t0009g0068 others(1): Show |
4 | HG03834.hp2 NA18944.hp1 NA18965.hp1 others(1): Show |
intron_variant | MODIFIER | c.248-510C>A | MFAP5 | ENSG00000197614.11 | transcript | ENST00000359478.7 | protein_coding | 7/9 | chr12 | 8651099 | |||||||
| chr12:8651124 | G | A | 4 | a0001c0001t0001g0016 a0001c0001t0001g0151 a0001c0001t0001g0158 others(1): Show |
7 | HG01891.hp2 HG02280.hp1 HG02572.hp2 others(4): Show |
intron_variant | MODIFIER | c.248-535C>T | MFAP5 | ENSG00000197614.11 | transcript | ENST00000359478.7 | protein_coding | 7/9 | chr12 | 8651124 | |||||||
| chr12:8651162 | A | G | 2 | a0001c0001t0003g0057 a0001c0001t0003g0206 |
3 | HG02109.hp1 HG02965.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.247+500T>C | MFAP5 | ENSG00000197614.11 | transcript | ENST00000359478.7 | protein_coding | 7/9 | chr12 | 8651162 | |||||||
| chr12:8651167 | A | C | 13 | a0001c0001t0003g0057 a0001c0001t0003g0206 a0001c0001t0004g0018 others(10): Show |
24 | HG00280.hp1 HG00323.hp2 HG00408.hp1 others(21): Show |
intron_variant | MODIFIER | c.247+495T>G | MFAP5 | ENSG00000197614.11 | transcript | ENST00000359478.7 | protein_coding | 7/9 | chr12 | 8651167 | |||||||
| chr12:8651386 | C | T | 11 | a0001c0001t0004g0018 a0001c0001t0004g0032 a0001c0001t0004g0033 others(8): Show |
21 | HG00280.hp1 HG00323.hp2 HG00408.hp1 others(18): Show |
intron_variant | MODIFIER | c.247+276G>A | MFAP5 | ENSG00000197614.11 | transcript | ENST00000359478.7 | protein_coding | 7/9 | chr12 | 8651386 | |||||||
| chr12:8651498 | A | G | 1 | a0001c0001t0001g0111 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.247+164T>C | MFAP5 | ENSG00000197614.11 | transcript | ENST00000359478.7 | protein_coding | 7/9 | chr12 | 8651498 | |||||||
| chr12:8651511 | A | G | 1 | a0001c0001t0012g0205 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.247+151T>C | MFAP5 | ENSG00000197614.11 | transcript | ENST00000359478.7 | protein_coding | 7/9 | chr12 | 8651511 | |||||||
| chr12:8651541 | T | C | 9 | a0001c0001t0003g0056 a0001c0001t0003g0196 a0001c0001t0003g0197 others(6): Show |
10 | HG01168.hp2 HG01169.hp1 HG01261.hp1 others(7): Show |
intron_variant | MODIFIER | c.247+121A>G | MFAP5 | ENSG00000197614.11 | transcript | ENST00000359478.7 | protein_coding | 7/9 | chr12 | 8651541 | |||||||
| chr12:8651623 | A | G | 1 | a0001c0001t0001g0188 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.247+39T>C | MFAP5 | ENSG00000197614.11 | transcript | ENST00000359478.7 | protein_coding | 7/9 | chr12 | 8651623 | |||||||
| chr12:8651786 | C | T | 2 | a0001c0001t0005g0034 a0001c0001t0005g0053 |
4 | HG02109.hp2 HG02723.hp2 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.218-95G>A | MFAP5 | ENSG00000197614.11 | transcript | ENST00000359478.7 | protein_coding | 6/9 | chr12 | 8651786 | |||||||
| chr12:8651976 | C | A | 11 | a0001c0001t0004g0018 a0001c0001t0004g0032 a0001c0001t0004g0033 others(8): Show |
21 | HG00280.hp1 HG00323.hp2 HG00408.hp1 others(18): Show |
intron_variant | MODIFIER | c.218-285G>T | MFAP5 | ENSG00000197614.11 | transcript | ENST00000359478.7 | protein_coding | 6/9 | chr12 | 8651976 | |||||||
| chr12:8652020 | A | C | 1 | a0001c0001t0001g0181 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.218-329T>G | MFAP5 | ENSG00000197614.11 | transcript | ENST00000359478.7 | protein_coding | 6/9 | chr12 | 8652020 | |||||||
| chr12:8652040 | C | T | 13 | a0001c0001t0003g0057 a0001c0001t0003g0206 a0001c0001t0004g0018 others(10): Show |
24 | HG00280.hp1 HG00323.hp2 HG00408.hp1 others(21): Show |
intron_variant | MODIFIER | c.218-349G>A | MFAP5 | ENSG00000197614.11 | transcript | ENST00000359478.7 | protein_coding | 6/9 | chr12 | 8652040 | |||||||
| chr12:8652216 | A | G | 2 | a0001c0001t0001g0086 a0001c0003t0012g0203 |
2 | HG01952.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.218-525T>C | MFAP5 | ENSG00000197614.11 | transcript | ENST00000359478.7 | protein_coding | 6/9 | chr12 | 8652216 | |||||||
| chr12:8652242 | T | C | 4 | a0001c0001t0001g0023 a0001c0001t0001g0095 a0001c0001t0001g0120 others(1): Show |
6 | NA18945.hp1 NA19007.hp2 NA19065.hp1 others(3): Show |
intron_variant | MODIFIER | c.218-551A>G | MFAP5 | ENSG00000197614.11 | transcript | ENST00000359478.7 | protein_coding | 6/9 | chr12 | 8652242 | |||||||
| chr12:8652299 | G | T | 1 | a0001c0001t0001g0192 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.218-608C>A | MFAP5 | ENSG00000197614.11 | transcript | ENST00000359478.7 | protein_coding | 6/9 | chr12 | 8652299 | |||||||
| chr12:8652350 | C | G | 6 | a0001c0001t0005g0034 a0001c0001t0005g0053 a0001c0001t0006g0084 others(3): Show |
8 | HG01891.hp1 HG02109.hp2 HG02622.hp2 others(5): Show |
intron_variant | MODIFIER | c.218-659G>C | MFAP5 | ENSG00000197614.11 | transcript | ENST00000359478.7 | protein_coding | 6/9 | chr12 | 8652350 | |||||||
| chr12:8652445 | A | AAAAT | 5 | a0001c0001t0006g0084 a0001c0001t0006g0171 a0001c0001t0006g0172 others(2): Show |
5 | HG01891.hp1 HG02622.hp2 HG02809.hp2 others(2): Show |
intron_variant | MODIFIER | c.218-758_218-755dup others(4): Show |
MFAP5 | ENSG00000197614.11 | transcript | ENST00000359478.7 | protein_coding | 6/9 | chr12 | 8652445 | |||||||
| chr12:8652445 | A | AAAATAAA others(1): Show |
6 | a0001c0001t0005g0034 a0001c0001t0005g0053 a0001c0001t0009g0066 others(3): Show |
8 | HG02109.hp2 HG02723.hp2 HG03139.hp1 others(5): Show |
intron_variant | MODIFIER | c.218-762_218-755dup others(8): Show |
MFAP5 | ENSG00000197614.11 | transcript | ENST00000359478.7 | protein_coding | 6/9 | chr12 | 8652445 | |||||||
| chr12:8652445 | AAAAT | A | 160 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(157): Show |
307 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(304): Show |
intron_variant | MODIFIER | c.218-758_218-755del others(4): Show |
MFAP5 | ENSG00000197614.11 | transcript | ENST00000359478.7 | protein_coding | 6/9 | chr12 | 8652445 | |||||||
| chr12:8652445 | AAAATAAA others(1): Show |
A | 13 | a0001c0001t0001g0071 a0001c0001t0001g0149 a0001c0001t0003g0057 others(10): Show |
22 | HG00280.hp1 HG00323.hp2 HG00408.hp1 others(19): Show |
intron_variant | MODIFIER | c.218-762_218-755del others(8): Show |
MFAP5 | ENSG00000197614.11 | transcript | ENST00000359478.7 | protein_coding | 6/9 | chr12 | 8652445 | |||||||
| chr12:8652477 | T | G | 1 | a0001c0001t0001g0088 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.218-786A>C | MFAP5 | ENSG00000197614.11 | transcript | ENST00000359478.7 | protein_coding | 6/9 | chr12 | 8652477 | |||||||
| chr12:8652491 | A | G | 32 | a0001c0001t0003g0056 a0001c0001t0003g0057 a0001c0001t0003g0196 others(29): Show |
44 | HG00280.hp1 HG00323.hp2 HG00408.hp1 others(41): Show |
intron_variant | MODIFIER | c.218-800T>C | MFAP5 | ENSG00000197614.11 | transcript | ENST00000359478.7 | protein_coding | 6/9 | chr12 | 8652491 | |||||||
| chr12:8652523 | G | A | 1 | a0001c0001t0005g0053 | 2 | HG02109.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.218-832C>T | MFAP5 | ENSG00000197614.11 | transcript | ENST00000359478.7 | protein_coding | 6/9 | chr12 | 8652523 | |||||||
| chr12:8652576 | C | T | 1 | a0001c0001t0008g0063 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.218-885G>A | MFAP5 | ENSG00000197614.11 | transcript | ENST00000359478.7 | protein_coding | 6/9 | chr12 | 8652576 | |||||||
| chr12:8652577 | A | G | 20 | a0001c0001t0003g0056 a0001c0001t0003g0057 a0001c0001t0003g0196 others(17): Show |
30 | HG00280.hp1 HG00323.hp2 HG00408.hp1 others(27): Show |
intron_variant | MODIFIER | c.218-886T>C | MFAP5 | ENSG00000197614.11 | transcript | ENST00000359478.7 | protein_coding | 6/9 | chr12 | 8652577 | |||||||
| chr12:8652592 | A | G | 177 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(174): Show |
305 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(302): Show |
intron_variant | MODIFIER | c.218-901T>C | MFAP5 | ENSG00000197614.11 | transcript | ENST00000359478.7 | protein_coding | 6/9 | chr12 | 8652592 | |||||||
| chr12:8652645 | T | G | 3 | a0001c0001t0001g0116 a0001c0001t0001g0117 a0001c0001t0001g0165 |
3 | NA18982.hp2 NA19067.hp1 NA19089.hp2 |
intron_variant | MODIFIER | c.218-954A>C | MFAP5 | ENSG00000197614.11 | transcript | ENST00000359478.7 | protein_coding | 6/9 | chr12 | 8652645 | |||||||
| chr12:8652702 | A | G | 2 | a0001c0001t0006g0105 a0001c0001t0017g0204 |
2 | HG02717.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.218-1011T>C | MFAP5 | ENSG00000197614.11 | transcript | ENST00000359478.7 | protein_coding | 6/9 | chr12 | 8652702 | |||||||
| chr12:8652745 | C | T | 1 | a0001c0001t0001g0116 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.218-1054G>A | MFAP5 | ENSG00000197614.11 | transcript | ENST00000359478.7 | protein_coding | 6/9 | chr12 | 8652745 | |||||||
| chr12:8652805 | A | C | 9 | a0001c0001t0003g0057 a0001c0001t0003g0206 a0001c0001t0004g0018 others(6): Show |
14 | HG00280.hp1 HG00323.hp2 HG01123.hp1 others(11): Show |
intron_variant | MODIFIER | c.218-1114T>G | MFAP5 | ENSG00000197614.11 | transcript | ENST00000359478.7 | protein_coding | 6/9 | chr12 | 8652805 | |||||||
| chr12:8652905 | C | T | 1 | a0001c0001t0001g0169 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.218-1214G>A | MFAP5 | ENSG00000197614.11 | transcript | ENST00000359478.7 | protein_coding | 6/9 | chr12 | 8652905 | |||||||
| chr12:8652933 | T | C | 6 | a0001c0001t0001g0019 a0001c0001t0001g0037 a0001c0001t0001g0075 others(3): Show |
9 | NA18946.hp1 NA18948.hp2 NA18950.hp2 others(6): Show |
intron_variant | MODIFIER | c.218-1242A>G | MFAP5 | ENSG00000197614.11 | transcript | ENST00000359478.7 | protein_coding | 6/9 | chr12 | 8652933 | |||||||
| chr12:8652952 | G | C | 12 | a0001c0001t0001g0035 a0001c0001t0001g0073 a0001c0001t0003g0057 others(9): Show |
18 | HG00280.hp1 HG00323.hp2 HG01123.hp1 others(15): Show |
intron_variant | MODIFIER | c.218-1261C>G | MFAP5 | ENSG00000197614.11 | transcript | ENST00000359478.7 | protein_coding | 6/9 | chr12 | 8652952 | |||||||
| chr12:8653147 | G | A | 1 | a0001c0001t0001g0146 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.217+1290C>T | MFAP5 | ENSG00000197614.11 | transcript | ENST00000359478.7 | protein_coding | 6/9 | chr12 | 8653147 | |||||||
| chr12:8653192 | C | CAA | 9 | a0001c0001t0001g0035 a0001c0001t0001g0073 a0001c0001t0004g0018 others(6): Show |
14 | HG00280.hp1 HG00323.hp2 HG01123.hp1 others(11): Show |
intron_variant | MODIFIER | c.217+1243_217+1244d others(4): Show |
MFAP5 | ENSG00000197614.11 | transcript | ENST00000359478.7 | protein_coding | 6/9 | chr12 | 8653192 | |||||||
| chr12:8653201 | A | G | 4 | a0001c0001t0003g0057 a0001c0001t0003g0206 a0001c0001t0006g0170 others(1): Show |
5 | HG02109.hp1 HG02572.hp2 HG02965.hp1 others(2): Show |
intron_variant | MODIFIER | c.217+1236T>C | MFAP5 | ENSG00000197614.11 | transcript | ENST00000359478.7 | protein_coding | 6/9 | chr12 | 8653201 | |||||||
| chr12:8653313 | C | T | 33 | a0001c0001t0001g0035 a0001c0001t0001g0073 a0001c0001t0003g0056 others(30): Show |
42 | HG00280.hp1 HG00323.hp2 HG01123.hp1 others(39): Show |
intron_variant | MODIFIER | c.217+1124G>A | MFAP5 | ENSG00000197614.11 | transcript | ENST00000359478.7 | protein_coding | 6/9 | chr12 | 8653313 | |||||||
| chr12:8653358 | G | A | 8 | a0001c0001t0003g0056 a0001c0001t0003g0196 a0001c0001t0003g0197 others(5): Show |
9 | HG01168.hp2 HG01169.hp1 HG01261.hp1 others(6): Show |
intron_variant | MODIFIER | c.217+1079C>T | MFAP5 | ENSG00000197614.11 | transcript | ENST00000359478.7 | protein_coding | 6/9 | chr12 | 8653358 | |||||||
| chr12:8653456 | A | G | 2 | a0001c0001t0001g0038 a0001c0001t0001g0135 |
3 | HG02300.hp1 HG02698.hp1 HG02738.hp2 |
intron_variant | MODIFIER | c.217+981T>C | MFAP5 | ENSG00000197614.11 | transcript | ENST00000359478.7 | protein_coding | 6/9 | chr12 | 8653456 | |||||||
| chr12:8653485 | G | A | 8 | a0001c0001t0003g0056 a0001c0001t0003g0196 a0001c0001t0003g0197 others(5): Show |
9 | HG01168.hp2 HG01169.hp1 HG01261.hp1 others(6): Show |
intron_variant | MODIFIER | c.217+952C>T | MFAP5 | ENSG00000197614.11 | transcript | ENST00000359478.7 | protein_coding | 6/9 | chr12 | 8653485 | |||||||
| chr12:8653495 | C | T | 2 | a0001c0001t0001g0142 a0001c0001t0001g0143 |
2 | NA18962.hp2 NA19062.hp2 |
intron_variant | MODIFIER | c.217+942G>A | MFAP5 | ENSG00000197614.11 | transcript | ENST00000359478.7 | protein_coding | 6/9 | chr12 | 8653495 | |||||||
| chr12:8653706 | G | A | 1 | a0001c0001t0001g0169 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.217+731C>T | MFAP5 | ENSG00000197614.11 | transcript | ENST00000359478.7 | protein_coding | 6/9 | chr12 | 8653706 | |||||||
| chr12:8653787 | C | A | 1 | a0001c0001t0001g0166 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.217+650G>T | MFAP5 | ENSG00000197614.11 | transcript | ENST00000359478.7 | protein_coding | 6/9 | chr12 | 8653787 | |||||||
| chr12:8653842 | T | C | 1 | a0001c0001t0001g0151 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.217+595A>G | MFAP5 | ENSG00000197614.11 | transcript | ENST00000359478.7 | protein_coding | 6/9 | chr12 | 8653842 | |||||||
| chr12:8653888 | G | A | 1 | a0001c0001t0006g0105 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.217+549C>T | MFAP5 | ENSG00000197614.11 | transcript | ENST00000359478.7 | protein_coding | 6/9 | chr12 | 8653888 | |||||||
| chr12:8653890 | C | T | 1 | a0001c0001t0006g0105 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.217+547G>A | MFAP5 | ENSG00000197614.11 | transcript | ENST00000359478.7 | protein_coding | 6/9 | chr12 | 8653890 | |||||||
| chr12:8653958 | C | T | 4 | a0001c0001t0009g0066 a0001c0001t0009g0067 a0001c0001t0009g0068 others(1): Show |
4 | HG03834.hp2 NA18944.hp1 NA18965.hp1 others(1): Show |
intron_variant | MODIFIER | c.217+479G>A | MFAP5 | ENSG00000197614.11 | transcript | ENST00000359478.7 | protein_coding | 6/9 | chr12 | 8653958 | |||||||
| chr12:8654014 | C | T | 22 | a0001c0001t0003g0057 a0001c0001t0003g0206 a0001c0001t0004g0018 others(19): Show |
29 | HG00280.hp1 HG00323.hp2 HG01123.hp1 others(26): Show |
intron_variant | MODIFIER | c.217+423G>A | MFAP5 | ENSG00000197614.11 | transcript | ENST00000359478.7 | protein_coding | 6/9 | chr12 | 8654014 | |||||||
| chr12:8654116 | T | G | 17 | a0001c0001t0003g0057 a0001c0001t0003g0206 a0001c0001t0004g0018 others(14): Show |
24 | HG00280.hp1 HG00323.hp2 HG01123.hp1 others(21): Show |
intron_variant | MODIFIER | c.217+321A>C | MFAP5 | ENSG00000197614.11 | transcript | ENST00000359478.7 | protein_coding | 6/9 | chr12 | 8654116 | |||||||
| chr12:8654126 | C | CA | 12 | a0001c0001t0001g0093 a0001c0001t0001g0118 a0001c0001t0001g0137 others(9): Show |
12 | HG00323.hp2 HG01257.hp2 HG02735.hp1 others(9): Show |
intron_variant | MODIFIER | c.217+310dupT | MFAP5 | ENSG00000197614.11 | transcript | ENST00000359478.7 | protein_coding | 6/9 | chr12 | 8654126 | |||||||
| chr12:8654126 | C | CAA | 15 | a0001c0001t0003g0057 a0001c0001t0003g0196 a0001c0001t0003g0197 others(12): Show |
20 | HG00280.hp1 HG01123.hp1 HG01169.hp1 others(17): Show |
intron_variant | MODIFIER | c.217+309_217+310dup others(2): Show |
MFAP5 | ENSG00000197614.11 | transcript | ENST00000359478.7 | protein_coding | 6/9 | chr12 | 8654126 | |||||||
| chr12:8654126 | C | CAAA | 7 | a0001c0001t0003g0056 a0001c0001t0003g0200 a0001c0001t0003g0202 others(4): Show |
10 | HG01168.hp2 HG02055.hp1 HG02109.hp2 others(7): Show |
intron_variant | MODIFIER | c.217+308_217+310dup others(3): Show |
MFAP5 | ENSG00000197614.11 | transcript | ENST00000359478.7 | protein_coding | 6/9 | chr12 | 8654126 | |||||||
| chr12:8654126 | CA | C | 13 | a0001c0001t0001g0026 a0001c0001t0001g0079 a0001c0001t0001g0082 others(10): Show |
16 | HG00558.hp1 HG00673.hp1 HG01074.hp1 others(13): Show |
intron_variant | MODIFIER | c.217+310delT | MFAP5 | ENSG00000197614.11 | transcript | ENST00000359478.7 | protein_coding | 6/9 | chr12 | 8654126 | |||||||
| chr12:8654154 | A | G | 13 | a0001c0001t0001g0035 a0001c0001t0001g0073 a0001c0001t0003g0057 others(10): Show |
19 | HG00280.hp1 HG00323.hp2 HG01123.hp1 others(16): Show |
intron_variant | MODIFIER | c.217+283T>C | MFAP5 | ENSG00000197614.11 | transcript | ENST00000359478.7 | protein_coding | 6/9 | chr12 | 8654154 | |||||||
| chr12:8654599 | T | C | 14 | a0001c0001t0001g0035 a0001c0001t0001g0073 a0001c0001t0003g0057 others(11): Show |
20 | HG00280.hp1 HG00323.hp2 HG01123.hp1 others(17): Show |
intron_variant | MODIFIER | c.173-118A>G | MFAP5 | ENSG00000197614.11 | transcript | ENST00000359478.7 | protein_coding | 5/9 | chr12 | 8654599 | |||||||
| chr12:8654777 | C | A | 1 | a0001c0001t0006g0170 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.173-296G>T | MFAP5 | ENSG00000197614.11 | transcript | ENST00000359478.7 | protein_coding | 5/9 | chr12 | 8654777 | |||||||
| chr12:8654792 | G | A | 14 | a0001c0001t0001g0035 a0001c0001t0001g0073 a0001c0001t0003g0057 others(11): Show |
20 | HG00280.hp1 HG00323.hp2 HG01123.hp1 others(17): Show |
intron_variant | MODIFIER | c.173-311C>T | MFAP5 | ENSG00000197614.11 | transcript | ENST00000359478.7 | protein_coding | 5/9 | chr12 | 8654792 | |||||||
| chr12:8654940 | C | CA | 8 | a0001c0001t0001g0072 a0001c0001t0001g0078 a0001c0001t0001g0126 others(5): Show |
8 | HG00735.hp1 HG02572.hp1 HG02717.hp1 others(5): Show |
intron_variant | MODIFIER | c.173-460dupT | MFAP5 | ENSG00000197614.11 | transcript | ENST00000359478.7 | protein_coding | 5/9 | chr12 | 8654940 | |||||||
| chr12:8654940 | C | CAAA | 9 | a0001c0001t0001g0035 a0001c0001t0001g0073 a0001c0001t0004g0018 others(6): Show |
14 | HG00280.hp1 HG00323.hp2 HG01123.hp1 others(11): Show |
intron_variant | MODIFIER | c.173-462_173-460dup others(3): Show |
MFAP5 | ENSG00000197614.11 | transcript | ENST00000359478.7 | protein_coding | 5/9 | chr12 | 8654940 | |||||||
| chr12:8654940 | C | CAAAA | 5 | a0001c0001t0005g0034 a0001c0001t0005g0053 a0001c0001t0006g0084 others(2): Show |
7 | HG01891.hp1 HG02109.hp2 HG02622.hp2 others(4): Show |
intron_variant | MODIFIER | c.173-463_173-460dup others(4): Show |
MFAP5 | ENSG00000197614.11 | transcript | ENST00000359478.7 | protein_coding | 5/9 | chr12 | 8654940 | |||||||
| chr12:8654940 | CA | C | 48 | a0001c0001t0001g0001 a0001c0001t0001g0012 a0001c0001t0001g0013 others(45): Show |
105 | HG00099.hp2 HG00323.hp1 HG00423.hp1 others(102): Show |
intron_variant | MODIFIER | c.173-460delT | MFAP5 | ENSG00000197614.11 | transcript | ENST00000359478.7 | protein_coding | 5/9 | chr12 | 8654940 | |||||||
| chr12:8654949 | A | G | 3 | a0001c0001t0001g0021 a0001c0001t0001g0111 a0001c0001t0001g0112 |
5 | HG02280.hp2 HG02451.hp1 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.172+466T>C | MFAP5 | ENSG00000197614.11 | transcript | ENST00000359478.7 | protein_coding | 5/9 | chr12 | 8654949 | |||||||
| chr12:8655038 | G | A | 6 | a0001c0001t0005g0034 a0001c0001t0005g0053 a0001c0001t0006g0084 others(3): Show |
8 | HG01891.hp1 HG02109.hp2 HG02622.hp2 others(5): Show |
intron_variant | MODIFIER | c.172+377C>T | MFAP5 | ENSG00000197614.11 | transcript | ENST00000359478.7 | protein_coding | 5/9 | chr12 | 8655038 | |||||||
| chr12:8655050 | C | T | 9 | a0001c0001t0001g0035 a0001c0001t0001g0073 a0001c0001t0004g0018 others(6): Show |
14 | HG00280.hp1 HG00323.hp2 HG01123.hp1 others(11): Show |
intron_variant | MODIFIER | c.172+365G>A | MFAP5 | ENSG00000197614.11 | transcript | ENST00000359478.7 | protein_coding | 5/9 | chr12 | 8655050 | |||||||
| chr12:8655107 | G | A | 20 | a0001c0001t0001g0035 a0001c0001t0001g0073 a0001c0001t0003g0057 others(17): Show |
28 | HG00280.hp1 HG00323.hp2 HG01123.hp1 others(25): Show |
intron_variant | MODIFIER | c.172+308C>T | MFAP5 | ENSG00000197614.11 | transcript | ENST00000359478.7 | protein_coding | 5/9 | chr12 | 8655107 | |||||||
| chr12:8655147 | G | A | 6 | a0001c0001t0003g0057 a0001c0001t0003g0206 a0001c0001t0006g0105 others(3): Show |
7 | HG02109.hp1 HG02572.hp2 HG02717.hp1 others(4): Show |
intron_variant | MODIFIER | c.172+268C>T | MFAP5 | ENSG00000197614.11 | transcript | ENST00000359478.7 | protein_coding | 5/9 | chr12 | 8655147 | |||||||
| chr12:8655386 | A | AT | 20 | a0001c0001t0001g0035 a0001c0001t0001g0073 a0001c0001t0003g0057 others(17): Show |
28 | HG00280.hp1 HG00323.hp2 HG01123.hp1 others(25): Show |
intron_variant | MODIFIER | c.172+28dupA | MFAP5 | ENSG00000197614.11 | transcript | ENST00000359478.7 | protein_coding | 5/9 | chr12 | 8655386 | |||||||
| chr12:8655410 | T | C | 119 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(116): Show |
181 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(178): Show |
splice_region_variant&intron_variant | LOW | c.172+5A>G | MFAP5 | ENSG00000197614.11 | transcript | ENST00000359478.7 | protein_coding | 5/9 | chr12 | 8655410 | |||||||
| chr12:8655528 | T | G | 1 | a0001c0001t0001g0052 | 2 | HG03490.hp1 HG03710.hp1 |
intron_variant | MODIFIER | c.140-81A>C | MFAP5 | ENSG00000197614.11 | transcript | ENST00000359478.7 | protein_coding | 4/9 | chr12 | 8655528 | |||||||
| chr12:8655626 | C | T | 13 | a0001c0001t0001g0004 a0001c0001t0001g0009 a0001c0001t0001g0090 others(10): Show |
22 | HG00544.hp1 HG00609.hp1 HG01071.hp2 others(19): Show |
intron_variant | MODIFIER | c.139+160G>A | MFAP5 | ENSG00000197614.11 | transcript | ENST00000359478.7 | protein_coding | 4/9 | chr12 | 8655626 | |||||||
| chr12:8655757 | A | G | 11 | a0001c0001t0005g0034 a0001c0001t0005g0053 a0001c0001t0006g0084 others(8): Show |
13 | HG01891.hp1 HG02109.hp2 HG02622.hp2 others(10): Show |
intron_variant | MODIFIER | c.139+29T>C | MFAP5 | ENSG00000197614.11 | transcript | ENST00000359478.7 | protein_coding | 4/9 | chr12 | 8655757 | |||||||
| chr12:8655766 | CAAACA | C | 11 | a0001c0001t0003g0057 a0001c0001t0003g0206 a0001c0001t0004g0018 others(8): Show |
16 | HG00280.hp1 HG00323.hp2 HG01123.hp1 others(13): Show |
intron_variant | MODIFIER | c.139+15_139+19delTG others(3): Show |
MFAP5 | ENSG00000197614.11 | transcript | ENST00000359478.7 | protein_coding | 4/9 | chr12 | 8655766 | |||||||
| chr12:8655859 | G | A | 2 | a0001c0001t0001g0140 a0001c0001t0001g0153 |
2 | HG01109.hp1 HG02257.hp1 |
intron_variant | MODIFIER | c.95-29C>T | MFAP5 | ENSG00000197614.11 | transcript | ENST00000359478.7 | protein_coding | 3/9 | chr12 | 8655859 | |||||||
| chr12:8655931 | T | G | 19 | a0001c0001t0003g0056 a0001c0001t0003g0196 a0001c0001t0003g0197 others(16): Show |
22 | HG01168.hp2 HG01169.hp1 HG01261.hp1 others(19): Show |
intron_variant | MODIFIER | c.95-101A>C | MFAP5 | ENSG00000197614.11 | transcript | ENST00000359478.7 | protein_coding | 3/9 | chr12 | 8655931 | |||||||
| chr12:8656034 | C | T | 9 | a0001c0001t0004g0018 a0001c0001t0004g0032 a0001c0001t0004g0033 others(6): Show |
13 | HG00280.hp1 HG00323.hp2 HG01123.hp1 others(10): Show |
intron_variant | MODIFIER | c.95-204G>A | MFAP5 | ENSG00000197614.11 | transcript | ENST00000359478.7 | protein_coding | 3/9 | chr12 | 8656034 | |||||||
| chr12:8656059 | C | CTTT | 6 | a0001c0001t0005g0034 a0001c0001t0005g0053 a0001c0001t0006g0170 others(3): Show |
8 | HG02109.hp2 HG02723.hp2 HG02965.hp1 others(5): Show |
intron_variant | MODIFIER | c.95-232_95-230dupAA others(1): Show |
MFAP5 | ENSG00000197614.11 | transcript | ENST00000359478.7 | protein_coding | 3/9 | chr12 | 8656059 | |||||||
| chr12:8656059 | C | CTTTT | 12 | a0001c0001t0003g0056 a0001c0001t0003g0196 a0001c0001t0003g0197 others(9): Show |
13 | HG01168.hp2 HG01169.hp1 HG01261.hp1 others(10): Show |
intron_variant | MODIFIER | c.95-233_95-230dupAA others(2): Show |
MFAP5 | ENSG00000197614.11 | transcript | ENST00000359478.7 | protein_coding | 3/9 | chr12 | 8656059 | |||||||
| chr12:8656059 | CT | C | 139 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(136): Show |
253 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(250): Show |
intron_variant | MODIFIER | c.95-230delA | MFAP5 | ENSG00000197614.11 | transcript | ENST00000359478.7 | protein_coding | 3/9 | chr12 | 8656059 | |||||||
| chr12:8656100 | G | A | 12 | a0001c0001t0003g0057 a0001c0001t0003g0206 a0001c0001t0004g0018 others(9): Show |
17 | HG00280.hp1 HG00323.hp2 HG01123.hp1 others(14): Show |
intron_variant | MODIFIER | c.95-270C>T | MFAP5 | ENSG00000197614.11 | transcript | ENST00000359478.7 | protein_coding | 3/9 | chr12 | 8656100 | |||||||
| chr12:8656156 | G | C | 11 | a0001c0001t0004g0018 a0001c0001t0004g0032 a0001c0001t0004g0033 others(8): Show |
17 | HG00280.hp1 HG00323.hp2 HG01123.hp1 others(14): Show |
intron_variant | MODIFIER | c.95-326C>G | MFAP5 | ENSG00000197614.11 | transcript | ENST00000359478.7 | protein_coding | 3/9 | chr12 | 8656156 | |||||||
| chr12:8656162 | A | G | 1 | a0001c0001t0001g0159 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.95-332T>C | MFAP5 | ENSG00000197614.11 | transcript | ENST00000359478.7 | protein_coding | 3/9 | chr12 | 8656162 | |||||||
| chr12:8656163 | T | C | 1 | a0001c0001t0001g0159 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.95-333A>G | MFAP5 | ENSG00000197614.11 | transcript | ENST00000359478.7 | protein_coding | 3/9 | chr12 | 8656163 | |||||||
| chr12:8656183 | C | T | 1 | a0001c0001t0008g0062 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.95-353G>A | MFAP5 | ENSG00000197614.11 | transcript | ENST00000359478.7 | protein_coding | 3/9 | chr12 | 8656183 | |||||||
| chr12:8656206 | G | A | 1 | a0001c0001t0017g0204 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.95-376C>T | MFAP5 | ENSG00000197614.11 | transcript | ENST00000359478.7 | protein_coding | 3/9 | chr12 | 8656206 | |||||||
| chr12:8656210 | G | A | 12 | a0001c0001t0003g0057 a0001c0001t0003g0206 a0001c0001t0004g0018 others(9): Show |
17 | HG00280.hp1 HG00323.hp2 HG01123.hp1 others(14): Show |
intron_variant | MODIFIER | c.95-380C>T | MFAP5 | ENSG00000197614.11 | transcript | ENST00000359478.7 | protein_coding | 3/9 | chr12 | 8656210 | |||||||
| chr12:8656215 | A | C | 1 | a0001c0001t0002g0132 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.95-385T>G | MFAP5 | ENSG00000197614.11 | transcript | ENST00000359478.7 | protein_coding | 3/9 | chr12 | 8656215 | |||||||
| chr12:8656216 | G | A | 1 | a0001c0001t0002g0132 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.95-386C>T | MFAP5 | ENSG00000197614.11 | transcript | ENST00000359478.7 | protein_coding | 3/9 | chr12 | 8656216 | |||||||
| chr12:8656219 | C | G | 1 | a0001c0001t0002g0132 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.95-389G>C | MFAP5 | ENSG00000197614.11 | transcript | ENST00000359478.7 | protein_coding | 3/9 | chr12 | 8656219 | |||||||
| chr12:8656283 | C | T | 12 | a0001c0001t0003g0057 a0001c0001t0003g0206 a0001c0001t0004g0018 others(9): Show |
17 | HG00280.hp1 HG00323.hp2 HG01123.hp1 others(14): Show |
intron_variant | MODIFIER | c.95-453G>A | MFAP5 | ENSG00000197614.11 | transcript | ENST00000359478.7 | protein_coding | 3/9 | chr12 | 8656283 | |||||||
| chr12:8656296 | C | G | 6 | a0001c0001t0003g0056 a0001c0001t0003g0196 a0001c0001t0003g0198 others(3): Show |
7 | HG01168.hp2 HG01169.hp1 HG02055.hp1 others(4): Show |
intron_variant | MODIFIER | c.95-466G>C | MFAP5 | ENSG00000197614.11 | transcript | ENST00000359478.7 | protein_coding | 3/9 | chr12 | 8656296 | |||||||
| chr12:8656335 | A | C | 1 | a0001c0001t0001g0049 | 2 | NA18984.hp2 NA19079.hp2 |
intron_variant | MODIFIER | c.95-505T>G | MFAP5 | ENSG00000197614.11 | transcript | ENST00000359478.7 | protein_coding | 3/9 | chr12 | 8656335 | |||||||
| chr12:8656344 | A | G | 28 | a0001c0001t0003g0056 a0001c0001t0003g0057 a0001c0001t0003g0196 others(25): Show |
34 | HG00280.hp1 HG00323.hp2 HG01123.hp1 others(31): Show |
intron_variant | MODIFIER | c.95-514T>C | MFAP5 | ENSG00000197614.11 | transcript | ENST00000359478.7 | protein_coding | 3/9 | chr12 | 8656344 | |||||||
| chr12:8656415 | GAT | G | 12 | a0001c0001t0003g0057 a0001c0001t0003g0206 a0001c0001t0004g0018 others(9): Show |
17 | HG00280.hp1 HG00323.hp2 HG01123.hp1 others(14): Show |
intron_variant | MODIFIER | c.95-587_95-586delAT | MFAP5 | ENSG00000197614.11 | transcript | ENST00000359478.7 | protein_coding | 3/9 | chr12 | 8656415 | |||||||
| chr12:8656416 | A | AT | 17 | a0001c0001t0001g0081 a0001c0001t0001g0110 a0001c0001t0001g0146 others(14): Show |
19 | HG01168.hp2 HG01169.hp1 HG01192.hp2 others(16): Show |
intron_variant | MODIFIER | c.95-587dupA | MFAP5 | ENSG00000197614.11 | transcript | ENST00000359478.7 | protein_coding | 3/9 | chr12 | 8656416 | |||||||
| chr12:8656416 | AT | A | 6 | a0001c0001t0001g0039 a0001c0001t0001g0085 a0001c0001t0001g0088 others(3): Show |
6 | HG02735.hp2 HG03017.hp1 HG03491.hp1 others(3): Show |
intron_variant | MODIFIER | c.95-587delA | MFAP5 | ENSG00000197614.11 | transcript | ENST00000359478.7 | protein_coding | 3/9 | chr12 | 8656416 | |||||||
| chr12:8656499 | T | C | 4 | a0001c0001t0009g0066 a0001c0001t0009g0067 a0001c0001t0009g0068 others(1): Show |
4 | HG03834.hp2 NA18944.hp1 NA18965.hp1 others(1): Show |
intron_variant | MODIFIER | c.95-669A>G | MFAP5 | ENSG00000197614.11 | transcript | ENST00000359478.7 | protein_coding | 3/9 | chr12 | 8656499 | |||||||
| chr12:8656573 | A | AAT | 20 | a0001c0001t0001g0005 a0001c0001t0001g0023 a0001c0001t0001g0045 others(17): Show |
30 | HG00438.hp2 HG00609.hp2 HG00673.hp2 others(27): Show |
intron_variant | MODIFIER | c.95-745_95-744dupAT | MFAP5 | ENSG00000197614.11 | transcript | ENST00000359478.7 | protein_coding | 3/9 | chr12 | 8656573 | |||||||
| chr12:8656573 | A | AATAT | 4 | a0001c0001t0001g0024 a0001c0001t0001g0048 a0001c0001t0001g0131 others(1): Show |
7 | HG03688.hp2 HG03831.hp2 NA18962.hp1 others(4): Show |
intron_variant | MODIFIER | c.95-747_95-744dupAT others(2): Show |
MFAP5 | ENSG00000197614.11 | transcript | ENST00000359478.7 | protein_coding | 3/9 | chr12 | 8656573 | |||||||
| chr12:8656573 | A | AATATATA others(7): Show |
1 | a0001c0001t0012g0205 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.95-757_95-744dupAT others(12): Show |
MFAP5 | ENSG00000197614.11 | transcript | ENST00000359478.7 | protein_coding | 3/9 | chr12 | 8656573 | |||||||
| chr12:8656573 | A | AATATATA others(9): Show |
1 | a0001c0001t0003g0196 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.95-759_95-744dupAT others(14): Show |
MFAP5 | ENSG00000197614.11 | transcript | ENST00000359478.7 | protein_coding | 3/9 | chr12 | 8656573 | |||||||
| chr12:8656573 | A | AATATATA others(11): Show |
4 | a0001c0001t0003g0056 a0001c0001t0003g0197 a0001c0001t0003g0200 others(1): Show |
5 | HG01261.hp1 HG02055.hp1 HG02145.hp1 others(2): Show |
intron_variant | MODIFIER | c.95-761_95-744dupAT others(16): Show |
MFAP5 | ENSG00000197614.11 | transcript | ENST00000359478.7 | protein_coding | 3/9 | chr12 | 8656573 | |||||||
| chr12:8656573 | A | AATATATA others(13): Show |
1 | a0001c0001t0003g0199 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.95-744_95-743insAT others(18): Show |
MFAP5 | ENSG00000197614.11 | transcript | ENST00000359478.7 | protein_coding | 3/9 | chr12 | 8656573 | |||||||
| chr12:8656573 | A | AATATATA others(15): Show |
2 | a0001c0001t0003g0198 a0001c0001t0003g0202 |
2 | HG01168.hp2 HG01169.hp1 |
intron_variant | MODIFIER | c.95-744_95-743insAT others(20): Show |
MFAP5 | ENSG00000197614.11 | transcript | ENST00000359478.7 | protein_coding | 3/9 | chr12 | 8656573 | |||||||
| chr12:8656583 | T | TATATACA others(17): Show |
10 | a0001c0001t0004g0018 a0001c0001t0004g0032 a0001c0001t0004g0033 others(7): Show |
14 | HG00280.hp1 HG00323.hp2 HG01123.hp1 others(11): Show |
intron_variant | MODIFIER | c.95-754_95-753insGT others(22): Show |
MFAP5 | ENSG00000197614.11 | transcript | ENST00000359478.7 | protein_coding | 3/9 | chr12 | 8656583 | |||||||
| chr12:8656589 | T | C | 1 | a0001c0001t0006g0171 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.95-759A>G | MFAP5 | ENSG00000197614.11 | transcript | ENST00000359478.7 | protein_coding | 3/9 | chr12 | 8656589 | |||||||
| chr12:8656591 | T | C | 4 | a0001c0001t0001g0112 a0001c0001t0001g0154 a0001c0001t0002g0100 others(1): Show |
4 | HG01123.hp2 HG02257.hp2 HG02809.hp2 others(1): Show |
intron_variant | MODIFIER | c.95-761A>G | MFAP5 | ENSG00000197614.11 | transcript | ENST00000359478.7 | protein_coding | 3/9 | chr12 | 8656591 | |||||||
| chr12:8656591 | T | TAC | 11 | a0001c0001t0001g0006 a0001c0001t0001g0030 a0001c0001t0001g0082 others(8): Show |
19 | HG02015.hp2 HG02040.hp1 HG02056.hp2 others(16): Show |
intron_variant | MODIFIER | c.95-763_95-762dupGT | MFAP5 | ENSG00000197614.11 | transcript | ENST00000359478.7 | protein_coding | 3/9 | chr12 | 8656591 | |||||||
| chr12:8656591 | T | TATAC | 4 | a0001c0001t0009g0066 a0001c0001t0009g0067 a0001c0001t0009g0068 others(1): Show |
4 | HG03834.hp2 NA18944.hp1 NA18965.hp1 others(1): Show |
intron_variant | MODIFIER | c.95-762_95-761insGT others(2): Show |
MFAP5 | ENSG00000197614.11 | transcript | ENST00000359478.7 | protein_coding | 3/9 | chr12 | 8656591 | |||||||
| chr12:8656593 | C | T | 14 | a0001c0001t0001g0044 a0001c0001t0001g0097 a0001c0001t0001g0115 others(11): Show |
16 | HG00673.hp1 HG01168.hp2 HG01169.hp1 others(13): Show |
intron_variant | MODIFIER | c.95-763G>A | MFAP5 | ENSG00000197614.11 | transcript | ENST00000359478.7 | protein_coding | 3/9 | chr12 | 8656593 | |||||||
| chr12:8656595 | C | T | 7 | a0001c0001t0003g0056 a0001c0001t0003g0196 a0001c0001t0003g0197 others(4): Show |
8 | HG01168.hp2 HG01169.hp1 HG01261.hp1 others(5): Show |
intron_variant | MODIFIER | c.95-765G>A | MFAP5 | ENSG00000197614.11 | transcript | ENST00000359478.7 | protein_coding | 3/9 | chr12 | 8656595 | |||||||
| chr12:8656597 | C | CACACACA others(21): Show |
1 | a0001c0001t0005g0034 | 2 | HG02723.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.95-795_95-768dupAT others(26): Show |
MFAP5 | ENSG00000197614.11 | transcript | ENST00000359478.7 | protein_coding | 3/9 | chr12 | 8656597 | |||||||
| chr12:8656597 | C | CAT | 10 | a0001c0001t0004g0018 a0001c0001t0004g0032 a0001c0001t0004g0033 others(7): Show |
14 | HG00280.hp1 HG00323.hp2 HG01123.hp1 others(11): Show |
intron_variant | MODIFIER | c.95-768_95-767insAT | MFAP5 | ENSG00000197614.11 | transcript | ENST00000359478.7 | protein_coding | 3/9 | chr12 | 8656597 | |||||||
| chr12:8656597 | C | T | 2 | a0001c0001t0003g0201 a0001c0001t0012g0205 |
2 | HG02572.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.95-767G>A | MFAP5 | ENSG00000197614.11 | transcript | ENST00000359478.7 | protein_coding | 3/9 | chr12 | 8656597 | |||||||
| chr12:8656603 | C | CATATATA others(1): Show |
2 | a0001c0001t0003g0057 a0001c0001t0003g0206 |
3 | HG02109.hp1 HG02965.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.95-774_95-773insAT others(6): Show |
MFAP5 | ENSG00000197614.11 | transcript | ENST00000359478.7 | protein_coding | 3/9 | chr12 | 8656603 | |||||||
| chr12:8656604 | A | ACACATAT others(19): Show |
1 | a0001c0001t0006g0171 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.95-775_95-774insCG others(24): Show |
MFAP5 | ENSG00000197614.11 | transcript | ENST00000359478.7 | protein_coding | 3/9 | chr12 | 8656604 | |||||||
| chr12:8656607 | C | T | 1 | a0001c0001t0017g0204 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.95-777G>A | MFAP5 | ENSG00000197614.11 | transcript | ENST00000359478.7 | protein_coding | 3/9 | chr12 | 8656607 | |||||||
| chr12:8656609 | C | T | 1 | a0001c0001t0017g0204 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.95-779G>A | MFAP5 | ENSG00000197614.11 | transcript | ENST00000359478.7 | protein_coding | 3/9 | chr12 | 8656609 | |||||||
| chr12:8656611 | T | C | 4 | a0001c0001t0009g0066 a0001c0001t0009g0067 a0001c0001t0009g0068 others(1): Show |
4 | HG03834.hp2 NA18944.hp1 NA18965.hp1 others(1): Show |
intron_variant | MODIFIER | c.95-781A>G | MFAP5 | ENSG00000197614.11 | transcript | ENST00000359478.7 | protein_coding | 3/9 | chr12 | 8656611 | |||||||
| chr12:8656613 | T | C | 2 | a0001c0001t0003g0057 a0001c0001t0003g0206 |
3 | HG02109.hp1 HG02965.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.95-783A>G | MFAP5 | ENSG00000197614.11 | transcript | ENST00000359478.7 | protein_coding | 3/9 | chr12 | 8656613 | |||||||
| chr12:8656615 | T | C | 3 | a0001c0001t0003g0057 a0001c0001t0003g0206 a0001c0001t0017g0204 |
4 | HG02109.hp1 HG02965.hp2 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.95-785A>G | MFAP5 | ENSG00000197614.11 | transcript | ENST00000359478.7 | protein_coding | 3/9 | chr12 | 8656615 | |||||||
| chr12:8656617 | T | C | 3 | a0001c0001t0003g0057 a0001c0001t0003g0206 a0001c0001t0017g0204 |
4 | HG02109.hp1 HG02965.hp2 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.95-787A>G | MFAP5 | ENSG00000197614.11 | transcript | ENST00000359478.7 | protein_coding | 3/9 | chr12 | 8656617 | |||||||
| chr12:8656625 | T | C | 3 | a0001c0001t0003g0057 a0001c0001t0003g0206 a0001c0001t0017g0204 |
4 | HG02109.hp1 HG02965.hp2 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.95-795A>G | MFAP5 | ENSG00000197614.11 | transcript | ENST00000359478.7 | protein_coding | 3/9 | chr12 | 8656625 | |||||||
| chr12:8656625 | T | TAC | 5 | a0001c0001t0001g0011 a0001c0001t0001g0093 a0001c0001t0001g0113 others(2): Show |
8 | HG01884.hp1 HG02165.hp2 HG02559.hp2 others(5): Show |
intron_variant | MODIFIER | c.95-797_95-796dupGT | MFAP5 | ENSG00000197614.11 | transcript | ENST00000359478.7 | protein_coding | 3/9 | chr12 | 8656625 | |||||||
| chr12:8656625 | T | TACACACA others(7): Show |
2 | a0001c0001t0003g0197 a0001c0001t0003g0201 |
2 | HG01261.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.95-809_95-796dupGT others(12): Show |
MFAP5 | ENSG00000197614.11 | transcript | ENST00000359478.7 | protein_coding | 3/9 | chr12 | 8656625 | |||||||
| chr12:8656625 | T | TACACACA others(15): Show |
1 | a0001c0001t0003g0202 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.95-817_95-796dupGT others(20): Show |
MFAP5 | ENSG00000197614.11 | transcript | ENST00000359478.7 | protein_coding | 3/9 | chr12 | 8656625 | |||||||
| chr12:8656625 | TACAC | T | 3 | a0001c0001t0001g0013 a0001c0001t0001g0129 a0001c0001t0001g0130 |
6 | HG00323.hp1 HG01496.hp1 HG01952.hp1 others(3): Show |
intron_variant | MODIFIER | c.95-799_95-796delGT others(2): Show |
MFAP5 | ENSG00000197614.11 | transcript | ENST00000359478.7 | protein_coding | 3/9 | chr12 | 8656625 | |||||||
| chr12:8656631 | C | CACACACA others(7): Show |
1 | a0001c0001t0006g0170 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.95-802_95-801insAT others(12): Show |
MFAP5 | ENSG00000197614.11 | transcript | ENST00000359478.7 | protein_coding | 3/9 | chr12 | 8656631 | |||||||
| chr12:8656639 | C | T | 13 | a0001c0001t0004g0018 a0001c0001t0004g0032 a0001c0001t0004g0033 others(10): Show |
18 | HG00280.hp1 HG00323.hp2 HG01123.hp1 others(15): Show |
intron_variant | MODIFIER | c.95-809G>A | MFAP5 | ENSG00000197614.11 | transcript | ENST00000359478.7 | protein_coding | 3/9 | chr12 | 8656639 | |||||||
| chr12:8656647 | C | T | 1 | a0001c0001t0001g0096 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.95-817G>A | MFAP5 | ENSG00000197614.11 | transcript | ENST00000359478.7 | protein_coding | 3/9 | chr12 | 8656647 | |||||||
| chr12:8656649 | C | CACACACA others(19): Show |
5 | a0001c0001t0003g0056 a0001c0001t0003g0196 a0001c0001t0003g0198 others(2): Show |
6 | HG01169.hp1 HG02055.hp1 HG02145.hp1 others(3): Show |
intron_variant | MODIFIER | c.95-820_95-819insAT others(24): Show |
MFAP5 | ENSG00000197614.11 | transcript | ENST00000359478.7 | protein_coding | 3/9 | chr12 | 8656649 | |||||||
| chr12:8656649 | C | CACACACA others(13): Show |
1 | a0001c0001t0012g0205 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.95-820_95-819insAT others(18): Show |
MFAP5 | ENSG00000197614.11 | transcript | ENST00000359478.7 | protein_coding | 3/9 | chr12 | 8656649 | |||||||
| chr12:8656649 | C | CACACACA others(5): Show |
1 | a0001c0001t0009g0068 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.95-820_95-819insAT others(10): Show |
MFAP5 | ENSG00000197614.11 | transcript | ENST00000359478.7 | protein_coding | 3/9 | chr12 | 8656649 | |||||||
| chr12:8656649 | C | CACACACA others(7): Show |
1 | a0001c0001t0009g0066 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.95-820_95-819insAT others(12): Show |
MFAP5 | ENSG00000197614.11 | transcript | ENST00000359478.7 | protein_coding | 3/9 | chr12 | 8656649 | |||||||
| chr12:8656649 | C | CACACAT | 3 | a0001c0001t0003g0057 a0001c0001t0003g0206 a0001c0001t0009g0067 |
4 | HG02109.hp1 HG02965.hp2 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.95-820_95-819insAT others(4): Show |
MFAP5 | ENSG00000197614.11 | transcript | ENST00000359478.7 | protein_coding | 3/9 | chr12 | 8656649 | |||||||
| chr12:8656649 | C | CAT | 7 | a0001c0001t0001g0019 a0001c0001t0001g0036 a0001c0001t0001g0037 others(4): Show |
11 | NA18946.hp1 NA18948.hp2 NA18950.hp2 others(8): Show |
intron_variant | MODIFIER | c.95-821_95-820dupAT | MFAP5 | ENSG00000197614.11 | transcript | ENST00000359478.7 | protein_coding | 3/9 | chr12 | 8656649 | |||||||
| chr12:8656649 | C | CATAT | 6 | a0001c0001t0001g0039 a0001c0001t0001g0040 a0001c0001t0001g0085 others(3): Show |
7 | HG02735.hp2 HG03017.hp1 HG03195.hp1 others(4): Show |
intron_variant | MODIFIER | c.95-823_95-820dupAT others(2): Show |
MFAP5 | ENSG00000197614.11 | transcript | ENST00000359478.7 | protein_coding | 3/9 | chr12 | 8656649 | |||||||
| chr12:8656649 | C | T | 2 | a0001c0001t0001g0015 a0001c0001t0001g0096 |
2 | NA19062.hp1 NA19085.hp1 |
intron_variant | MODIFIER | c.95-819G>A | MFAP5 | ENSG00000197614.11 | transcript | ENST00000359478.7 | protein_coding | 3/9 | chr12 | 8656649 | |||||||
| chr12:8656651 | T | C | 91 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(88): Show |
144 | HG00140.hp1 HG00280.hp2 HG00408.hp1 others(141): Show |
intron_variant | MODIFIER | c.95-821A>G | MFAP5 | ENSG00000197614.11 | transcript | ENST00000359478.7 | protein_coding | 3/9 | chr12 | 8656651 | |||||||
| chr12:8656653 | T | C | 7 | a0001c0001t0001g0030 a0001c0001t0001g0122 a0001c0001t0001g0178 others(4): Show |
9 | HG02015.hp2 HG03654.hp1 NA18940.hp1 others(6): Show |
intron_variant | MODIFIER | c.95-823A>G | MFAP5 | ENSG00000197614.11 | transcript | ENST00000359478.7 | protein_coding | 3/9 | chr12 | 8656653 | |||||||
| chr12:8656666 | A | ATTTT | 8 | a0001c0001t0004g0018 a0001c0001t0004g0032 a0001c0001t0004g0033 others(5): Show |
11 | HG00280.hp1 HG00323.hp2 HG01123.hp1 others(8): Show |
intron_variant | MODIFIER | c.95-837_95-836insAA others(2): Show |
MFAP5 | ENSG00000197614.11 | transcript | ENST00000359478.7 | protein_coding | 3/9 | chr12 | 8656666 | |||||||
| chr12:8656666 | A | T | 16 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0012 others(13): Show |
18 | HG01167.hp1 HG01169.hp1 HG01169.hp2 others(15): Show |
intron_variant | MODIFIER | c.95-836T>A | MFAP5 | ENSG00000197614.11 | transcript | ENST00000359478.7 | protein_coding | 3/9 | chr12 | 8656666 | |||||||
| chr12:8656668 | A | ATATATAT others(15): Show |
1 | a0001c0001t0015g0128 | 1 | NA19085.hp2 | intron_variant | MODIFIER | c.95-839_95-838insAA others(20): Show |
MFAP5 | ENSG00000197614.11 | transcript | ENST00000359478.7 | protein_coding | 3/9 | chr12 | 8656668 | |||||||
| chr12:8656668 | A | ATTT | 5 | a0001c0001t0003g0057 a0001c0001t0003g0202 a0001c0001t0003g0206 others(2): Show |
7 | HG01168.hp2 HG02109.hp1 HG02572.hp2 others(4): Show |
intron_variant | MODIFIER | c.95-841_95-839dupAA others(1): Show |
MFAP5 | ENSG00000197614.11 | transcript | ENST00000359478.7 | protein_coding | 3/9 | chr12 | 8656668 | |||||||
| chr12:8656668 | A | ATTTTTTT others(9): Show |
2 | a0001c0001t0009g0066 a0001c0001t0009g0068 |
2 | NA18944.hp1 NA18965.hp1 |
intron_variant | MODIFIER | c.95-839_95-838insAA others(14): Show |
MFAP5 | ENSG00000197614.11 | transcript | ENST00000359478.7 | protein_coding | 3/9 | chr12 | 8656668 | |||||||
| chr12:8656668 | A | ATTTTTTT others(11): Show |
1 | a0001c0001t0009g0067 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.95-839_95-838insAA others(16): Show |
MFAP5 | ENSG00000197614.11 | transcript | ENST00000359478.7 | protein_coding | 3/9 | chr12 | 8656668 | |||||||
| chr12:8656668 | A | T | 57 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0012 others(54): Show |
118 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(115): Show |
intron_variant | MODIFIER | c.95-838T>A | MFAP5 | ENSG00000197614.11 | transcript | ENST00000359478.7 | protein_coding | 3/9 | chr12 | 8656668 | |||||||
| chr12:8656670 | T | A | 84 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(81): Show |
136 | HG00140.hp1 HG00280.hp2 HG00408.hp1 others(133): Show |
intron_variant | MODIFIER | c.95-840A>T | MFAP5 | ENSG00000197614.11 | transcript | ENST00000359478.7 | protein_coding | 3/9 | chr12 | 8656670 | |||||||
| chr12:8656672 | T | A | 36 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(33): Show |
62 | HG00280.hp2 HG00609.hp2 HG00673.hp1 others(59): Show |
intron_variant | MODIFIER | c.95-842A>T | MFAP5 | ENSG00000197614.11 | transcript | ENST00000359478.7 | protein_coding | 3/9 | chr12 | 8656672 | |||||||
| chr12:8656674 | T | A | 1 | a0001c0001t0001g0123 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.95-844A>T | MFAP5 | ENSG00000197614.11 | transcript | ENST00000359478.7 | protein_coding | 3/9 | chr12 | 8656674 | |||||||
| chr12:8656693 | G | C | 4 | a0001c0001t0009g0066 a0001c0001t0009g0067 a0001c0001t0009g0068 others(1): Show |
4 | HG03834.hp2 NA18944.hp1 NA18965.hp1 others(1): Show |
intron_variant | MODIFIER | c.95-863C>G | MFAP5 | ENSG00000197614.11 | transcript | ENST00000359478.7 | protein_coding | 3/9 | chr12 | 8656693 | |||||||
| chr12:8656725 | A | G | 17 | a0001c0001t0004g0018 a0001c0001t0004g0032 a0001c0001t0004g0033 others(14): Show |
22 | HG00280.hp1 HG00323.hp2 HG01123.hp1 others(19): Show |
intron_variant | MODIFIER | c.95-895T>C | MFAP5 | ENSG00000197614.11 | transcript | ENST00000359478.7 | protein_coding | 3/9 | chr12 | 8656725 | |||||||
| chr12:8656773 | A | G | 4 | a0001c0001t0009g0066 a0001c0001t0009g0067 a0001c0001t0009g0068 others(1): Show |
4 | HG03834.hp2 NA18944.hp1 NA18965.hp1 others(1): Show |
intron_variant | MODIFIER | c.95-943T>C | MFAP5 | ENSG00000197614.11 | transcript | ENST00000359478.7 | protein_coding | 3/9 | chr12 | 8656773 | |||||||
| chr12:8656853 | A | G | 4 | a0001c0001t0009g0066 a0001c0001t0009g0067 a0001c0001t0009g0068 others(1): Show |
4 | HG03834.hp2 NA18944.hp1 NA18965.hp1 others(1): Show |
intron_variant | MODIFIER | c.95-1023T>C | MFAP5 | ENSG00000197614.11 | transcript | ENST00000359478.7 | protein_coding | 3/9 | chr12 | 8656853 | |||||||
| chr12:8657064 | T | A | 8 | a0001c0001t0004g0018 a0001c0001t0004g0032 a0001c0001t0004g0033 others(5): Show |
12 | HG00280.hp1 HG00323.hp2 HG01123.hp1 others(9): Show |
intron_variant | MODIFIER | c.95-1234A>T | MFAP5 | ENSG00000197614.11 | transcript | ENST00000359478.7 | protein_coding | 3/9 | chr12 | 8657064 | |||||||
| chr12:8657131 | G | A | 1 | a0001c0001t0005g0043 | 2 | HG04115.hp1 NA20905.hp2 |
intron_variant | MODIFIER | c.95-1301C>T | MFAP5 | ENSG00000197614.11 | transcript | ENST00000359478.7 | protein_coding | 3/9 | chr12 | 8657131 | |||||||
| chr12:8657182 | T | C | 52 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0011 others(49): Show |
81 | HG00140.hp1 HG00280.hp2 HG00438.hp2 others(78): Show |
intron_variant | MODIFIER | c.95-1352A>G | MFAP5 | ENSG00000197614.11 | transcript | ENST00000359478.7 | protein_coding | 3/9 | chr12 | 8657182 | |||||||
| chr12:8657223 | C | T | 3 | a0001c0001t0009g0066 a0001c0001t0009g0067 a0001c0001t0009g0068 |
3 | HG03834.hp2 NA18944.hp1 NA18965.hp1 |
intron_variant | MODIFIER | c.95-1393G>A | MFAP5 | ENSG00000197614.11 | transcript | ENST00000359478.7 | protein_coding | 3/9 | chr12 | 8657223 | |||||||
| chr12:8657250 | A | G | 2 | a0001c0001t0003g0198 a0001c0001t0003g0202 |
2 | HG01168.hp2 HG01169.hp1 |
intron_variant | MODIFIER | c.95-1420T>C | MFAP5 | ENSG00000197614.11 | transcript | ENST00000359478.7 | protein_coding | 3/9 | chr12 | 8657250 | |||||||
| chr12:8657322 | G | A | 1 | a0001c0001t0001g0079 | 1 | NA19065.hp2 | intron_variant | MODIFIER | c.95-1492C>T | MFAP5 | ENSG00000197614.11 | transcript | ENST00000359478.7 | protein_coding | 3/9 | chr12 | 8657322 | |||||||
| chr12:8657411 | C | A | 13 | a0001c0001t0004g0018 a0001c0001t0004g0032 a0001c0001t0004g0033 others(10): Show |
18 | HG00280.hp1 HG00323.hp2 HG01123.hp1 others(15): Show |
intron_variant | MODIFIER | c.95-1581G>T | MFAP5 | ENSG00000197614.11 | transcript | ENST00000359478.7 | protein_coding | 3/9 | chr12 | 8657411 | |||||||
| chr12:8657566 | C | CT | 14 | a0001c0001t0001g0012 a0001c0001t0001g0055 a0001c0001t0001g0075 others(11): Show |
18 | HG00639.hp2 HG01891.hp1 HG01993.hp2 others(15): Show |
intron_variant | MODIFIER | c.95-1737dupA | MFAP5 | ENSG00000197614.11 | transcript | ENST00000359478.7 | protein_coding | 3/9 | chr12 | 8657566 | |||||||
| chr12:8657566 | CT | C | 24 | a0001c0001t0001g0083 a0001c0001t0001g0158 a0001c0001t0001g0159 others(21): Show |
26 | HG01168.hp1 HG01168.hp2 HG01169.hp1 others(23): Show |
intron_variant | MODIFIER | c.95-1737delA | MFAP5 | ENSG00000197614.11 | transcript | ENST00000359478.7 | protein_coding | 3/9 | chr12 | 8657566 | |||||||
| chr12:8657566 | CTT | C | 10 | a0001c0001t0003g0057 a0001c0001t0003g0206 a0001c0001t0004g0018 others(7): Show |
15 | HG00280.hp1 HG01123.hp1 HG01257.hp2 others(12): Show |
intron_variant | MODIFIER | c.95-1738_95-1737del others(2): Show |
MFAP5 | ENSG00000197614.11 | transcript | ENST00000359478.7 | protein_coding | 3/9 | chr12 | 8657566 | |||||||
| chr12:8657593 | G | C | 3 | a0001c0001t0003g0057 a0001c0001t0003g0206 a0001c0001t0012g0205 |
4 | HG02109.hp1 HG02572.hp2 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.95-1763C>G | MFAP5 | ENSG00000197614.11 | transcript | ENST00000359478.7 | protein_coding | 3/9 | chr12 | 8657593 | |||||||
| chr12:8657609 | G | A | 17 | a0001c0001t0004g0018 a0001c0001t0004g0032 a0001c0001t0004g0033 others(14): Show |
22 | HG00280.hp1 HG00323.hp2 HG01123.hp1 others(19): Show |
intron_variant | MODIFIER | c.95-1779C>T | MFAP5 | ENSG00000197614.11 | transcript | ENST00000359478.7 | protein_coding | 3/9 | chr12 | 8657609 | |||||||
| chr12:8657710 | C | CT | 25 | a0001c0001t0003g0056 a0001c0001t0003g0196 a0001c0001t0003g0197 others(22): Show |
31 | HG00280.hp1 HG00323.hp2 HG01123.hp1 others(28): Show |
intron_variant | MODIFIER | c.95-1881_95-1880ins others(1): Show |
MFAP5 | ENSG00000197614.11 | transcript | ENST00000359478.7 | protein_coding | 3/9 | chr12 | 8657710 | |||||||
| chr12:8657717 | A | G | 28 | a0001c0001t0003g0056 a0001c0001t0003g0057 a0001c0001t0003g0196 others(25): Show |
35 | HG00280.hp1 HG00323.hp2 HG01123.hp1 others(32): Show |
intron_variant | MODIFIER | c.95-1887T>C | MFAP5 | ENSG00000197614.11 | transcript | ENST00000359478.7 | protein_coding | 3/9 | chr12 | 8657717 | |||||||
| chr12:8657868 | G | T | 1 | a0001c0001t0001g0035 | 2 | HG01192.hp1 HG01243.hp1 |
intron_variant | MODIFIER | c.95-2038C>A | MFAP5 | ENSG00000197614.11 | transcript | ENST00000359478.7 | protein_coding | 3/9 | chr12 | 8657868 | |||||||
| chr12:8657913 | A | G | 16 | a0001c0001t0004g0018 a0001c0001t0004g0032 a0001c0001t0004g0033 others(13): Show |
21 | HG00280.hp1 HG00323.hp2 HG01123.hp1 others(18): Show |
intron_variant | MODIFIER | c.95-2083T>C | MFAP5 | ENSG00000197614.11 | transcript | ENST00000359478.7 | protein_coding | 3/9 | chr12 | 8657913 | |||||||
| chr12:8658004 | T | C | 13 | a0001c0001t0004g0018 a0001c0001t0004g0032 a0001c0001t0004g0033 others(10): Show |
18 | HG00280.hp1 HG00323.hp2 HG01123.hp1 others(15): Show |
intron_variant | MODIFIER | c.95-2174A>G | MFAP5 | ENSG00000197614.11 | transcript | ENST00000359478.7 | protein_coding | 3/9 | chr12 | 8658004 | |||||||
| chr12:8658018 | G | A | 1 | a0001c0001t0012g0205 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.95-2188C>T | MFAP5 | ENSG00000197614.11 | transcript | ENST00000359478.7 | protein_coding | 3/9 | chr12 | 8658018 | |||||||
| chr12:8658101 | C | G | 1 | a0001c0001t0003g0197 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.95-2271G>C | MFAP5 | ENSG00000197614.11 | transcript | ENST00000359478.7 | protein_coding | 3/9 | chr12 | 8658101 | |||||||
| chr12:8658124 | G | A | 3 | a0001c0001t0009g0066 a0001c0001t0009g0067 a0001c0001t0009g0068 |
3 | HG03834.hp2 NA18944.hp1 NA18965.hp1 |
intron_variant | MODIFIER | c.95-2294C>T | MFAP5 | ENSG00000197614.11 | transcript | ENST00000359478.7 | protein_coding | 3/9 | chr12 | 8658124 | |||||||
| chr12:8658232 | C | T | 9 | a0001c0001t0003g0056 a0001c0001t0003g0196 a0001c0001t0003g0197 others(6): Show |
10 | HG01168.hp2 HG01169.hp1 HG01261.hp1 others(7): Show |
intron_variant | MODIFIER | c.95-2402G>A | MFAP5 | ENSG00000197614.11 | transcript | ENST00000359478.7 | protein_coding | 3/9 | chr12 | 8658232 | |||||||
| chr12:8658311 | C | T | 1 | a0001c0001t0001g0091 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.95-2481G>A | MFAP5 | ENSG00000197614.11 | transcript | ENST00000359478.7 | protein_coding | 3/9 | chr12 | 8658311 | |||||||
| chr12:8658344 | C | G | 1 | a0001c0001t0001g0125 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.95-2514G>C | MFAP5 | ENSG00000197614.11 | transcript | ENST00000359478.7 | protein_coding | 3/9 | chr12 | 8658344 | |||||||
| chr12:8658434 | T | A | 3 | a0001c0001t0009g0066 a0001c0001t0009g0067 a0001c0001t0009g0068 |
3 | HG03834.hp2 NA18944.hp1 NA18965.hp1 |
intron_variant | MODIFIER | c.94+2429A>T | MFAP5 | ENSG00000197614.11 | transcript | ENST00000359478.7 | protein_coding | 3/9 | chr12 | 8658434 | |||||||
| chr12:8658454 | G | A | 13 | a0001c0001t0004g0018 a0001c0001t0004g0032 a0001c0001t0004g0033 others(10): Show |
18 | HG00280.hp1 HG00323.hp2 HG01123.hp1 others(15): Show |
intron_variant | MODIFIER | c.94+2409C>T | MFAP5 | ENSG00000197614.11 | transcript | ENST00000359478.7 | protein_coding | 3/9 | chr12 | 8658454 | |||||||
| chr12:8658629 | A | G | 3 | a0001c0001t0009g0066 a0001c0001t0009g0067 a0001c0001t0009g0068 |
3 | HG03834.hp2 NA18944.hp1 NA18965.hp1 |
intron_variant | MODIFIER | c.94+2234T>C | MFAP5 | ENSG00000197614.11 | transcript | ENST00000359478.7 | protein_coding | 3/9 | chr12 | 8658629 | |||||||
| chr12:8658662 | G | A | 28 | a0001c0001t0003g0056 a0001c0001t0003g0057 a0001c0001t0003g0196 others(25): Show |
35 | HG00280.hp1 HG00323.hp2 HG01123.hp1 others(32): Show |
intron_variant | MODIFIER | c.94+2201C>T | MFAP5 | ENSG00000197614.11 | transcript | ENST00000359478.7 | protein_coding | 3/9 | chr12 | 8658662 | |||||||
| chr12:8658667 | A | T | 16 | a0001c0001t0004g0018 a0001c0001t0004g0032 a0001c0001t0004g0033 others(13): Show |
21 | HG00280.hp1 HG00323.hp2 HG01123.hp1 others(18): Show |
intron_variant | MODIFIER | c.94+2196T>A | MFAP5 | ENSG00000197614.11 | transcript | ENST00000359478.7 | protein_coding | 3/9 | chr12 | 8658667 | |||||||
| chr12:8658768 | C | T | 1 | a0001c0001t0001g0090 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.94+2095G>A | MFAP5 | ENSG00000197614.11 | transcript | ENST00000359478.7 | protein_coding | 3/9 | chr12 | 8658768 | |||||||
| chr12:8658776 | A | G | 1 | a0001c0001t0001g0124 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.94+2087T>C | MFAP5 | ENSG00000197614.11 | transcript | ENST00000359478.7 | protein_coding | 3/9 | chr12 | 8658776 | |||||||
| chr12:8658778 | G | A | 13 | a0001c0001t0004g0018 a0001c0001t0004g0032 a0001c0001t0004g0033 others(10): Show |
18 | HG00280.hp1 HG00323.hp2 HG01123.hp1 others(15): Show |
intron_variant | MODIFIER | c.94+2085C>T | MFAP5 | ENSG00000197614.11 | transcript | ENST00000359478.7 | protein_coding | 3/9 | chr12 | 8658778 | |||||||
| chr12:8658992 | C | CT | 94 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(91): Show |
152 | HG00140.hp1 HG00280.hp2 HG00408.hp1 others(149): Show |
intron_variant | MODIFIER | c.94+1870dupA | MFAP5 | ENSG00000197614.11 | transcript | ENST00000359478.7 | protein_coding | 3/9 | chr12 | 8658992 | |||||||
| chr12:8658992 | C | CTT | 8 | a0001c0001t0001g0089 a0001c0001t0001g0179 a0001c0001t0001g0187 others(5): Show |
9 | HG02145.hp2 HG02622.hp2 HG02723.hp2 others(6): Show |
intron_variant | MODIFIER | c.94+1869_94+1870dup others(2): Show |
MFAP5 | ENSG00000197614.11 | transcript | ENST00000359478.7 | protein_coding | 3/9 | chr12 | 8658992 | |||||||
| chr12:8658992 | C | CTTTT | 8 | a0001c0001t0004g0018 a0001c0001t0004g0032 a0001c0001t0004g0033 others(5): Show |
12 | HG00280.hp1 HG00323.hp2 HG01123.hp1 others(9): Show |
intron_variant | MODIFIER | c.94+1867_94+1870dup others(4): Show |
MFAP5 | ENSG00000197614.11 | transcript | ENST00000359478.7 | protein_coding | 3/9 | chr12 | 8658992 | |||||||
| chr12:8659056 | C | T | 12 | a0001c0001t0001g0039 a0001c0001t0001g0055 a0001c0001t0001g0085 others(9): Show |
14 | HG01891.hp1 HG01952.hp2 HG02055.hp2 others(11): Show |
intron_variant | MODIFIER | c.94+1807G>A | MFAP5 | ENSG00000197614.11 | transcript | ENST00000359478.7 | protein_coding | 3/9 | chr12 | 8659056 | |||||||
| chr12:8659127 | G | A | 1 | a0001c0001t0017g0204 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.94+1736C>T | MFAP5 | ENSG00000197614.11 | transcript | ENST00000359478.7 | protein_coding | 3/9 | chr12 | 8659127 | |||||||
| chr12:8659135 | C | G | 8 | a0001c0001t0004g0018 a0001c0001t0004g0032 a0001c0001t0004g0033 others(5): Show |
12 | HG00280.hp1 HG00323.hp2 HG01123.hp1 others(9): Show |
intron_variant | MODIFIER | c.94+1728G>C | MFAP5 | ENSG00000197614.11 | transcript | ENST00000359478.7 | protein_coding | 3/9 | chr12 | 8659135 | |||||||
| chr12:8659176 | C | T | 3 | a0001c0001t0003g0057 a0001c0001t0003g0206 a0001c0001t0012g0205 |
4 | HG02109.hp1 HG02572.hp2 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.94+1687G>A | MFAP5 | ENSG00000197614.11 | transcript | ENST00000359478.7 | protein_coding | 3/9 | chr12 | 8659176 | |||||||
| chr12:8659234 | G | A | 13 | a0001c0001t0004g0018 a0001c0001t0004g0032 a0001c0001t0004g0033 others(10): Show |
18 | HG00280.hp1 HG00323.hp2 HG01123.hp1 others(15): Show |
intron_variant | MODIFIER | c.94+1629C>T | MFAP5 | ENSG00000197614.11 | transcript | ENST00000359478.7 | protein_coding | 3/9 | chr12 | 8659234 | |||||||
| chr12:8659309 | GA | G | 7 | a0001c0001t0001g0082 a0001c0001t0001g0083 a0001c0001t0001g0178 others(4): Show |
8 | HG01168.hp1 HG02109.hp1 HG02572.hp2 others(5): Show |
intron_variant | MODIFIER | c.94+1553delT | MFAP5 | ENSG00000197614.11 | transcript | ENST00000359478.7 | protein_coding | 3/9 | chr12 | 8659309 | |||||||
| chr12:8659319 | A | T | 1 | a0001c0001t0001g0081 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.94+1544T>A | MFAP5 | ENSG00000197614.11 | transcript | ENST00000359478.7 | protein_coding | 3/9 | chr12 | 8659319 | |||||||
| chr12:8659321 | A | G | 3 | a0001c0001t0003g0057 a0001c0001t0003g0206 a0001c0001t0012g0205 |
4 | HG02109.hp1 HG02572.hp2 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.94+1542T>C | MFAP5 | ENSG00000197614.11 | transcript | ENST00000359478.7 | protein_coding | 3/9 | chr12 | 8659321 | |||||||
| chr12:8659324 | T | A | 3 | a0001c0001t0009g0066 a0001c0001t0009g0067 a0001c0001t0009g0068 |
3 | HG03834.hp2 NA18944.hp1 NA18965.hp1 |
intron_variant | MODIFIER | c.94+1539A>T | MFAP5 | ENSG00000197614.11 | transcript | ENST00000359478.7 | protein_coding | 3/9 | chr12 | 8659324 | |||||||
| chr12:8659341 | A | G | 16 | a0001c0001t0004g0018 a0001c0001t0004g0032 a0001c0001t0004g0033 others(13): Show |
21 | HG00280.hp1 HG00323.hp2 HG01123.hp1 others(18): Show |
intron_variant | MODIFIER | c.94+1522T>C | MFAP5 | ENSG00000197614.11 | transcript | ENST00000359478.7 | protein_coding | 3/9 | chr12 | 8659341 | |||||||
| chr12:8659388 | C | A | 3 | a0001c0001t0009g0066 a0001c0001t0009g0067 a0001c0001t0009g0068 |
3 | HG03834.hp2 NA18944.hp1 NA18965.hp1 |
intron_variant | MODIFIER | c.94+1475G>T | MFAP5 | ENSG00000197614.11 | transcript | ENST00000359478.7 | protein_coding | 3/9 | chr12 | 8659388 | |||||||
| chr12:8659725 | A | ATATAT | 4 | a0001c0001t0005g0034 a0001c0001t0009g0066 a0001c0001t0009g0067 others(1): Show |
5 | HG02723.hp2 HG03139.hp1 HG03834.hp2 others(2): Show |
intron_variant | MODIFIER | c.94+1137_94+1138ins others(5): Show |
MFAP5 | ENSG00000197614.11 | transcript | ENST00000359478.7 | protein_coding | 3/9 | chr12 | 8659725 | |||||||
| chr12:8659818 | A | G | 4 | a0001c0001t0005g0034 a0001c0001t0009g0066 a0001c0001t0009g0067 others(1): Show |
5 | HG02723.hp2 HG03139.hp1 HG03834.hp2 others(2): Show |
intron_variant | MODIFIER | c.94+1045T>C | MFAP5 | ENSG00000197614.11 | transcript | ENST00000359478.7 | protein_coding | 3/9 | chr12 | 8659818 | |||||||
| chr12:8659890 | A | G | 1 | a0001c0001t0017g0204 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.94+973T>C | MFAP5 | ENSG00000197614.11 | transcript | ENST00000359478.7 | protein_coding | 3/9 | chr12 | 8659890 | |||||||
| chr12:8660024 | A | G | 2 | a0001c0001t0001g0038 a0001c0001t0001g0080 |
3 | HG02300.hp1 HG02698.hp1 HG04204.hp2 |
intron_variant | MODIFIER | c.94+839T>C | MFAP5 | ENSG00000197614.11 | transcript | ENST00000359478.7 | protein_coding | 3/9 | chr12 | 8660024 | |||||||
| chr12:8660053 | C | T | 1 | a0001c0001t0017g0204 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.94+810G>A | MFAP5 | ENSG00000197614.11 | transcript | ENST00000359478.7 | protein_coding | 3/9 | chr12 | 8660053 | |||||||
| chr12:8660191 | AT | A | 32 | a0001c0001t0001g0073 a0001c0001t0001g0161 a0001c0001t0001g0162 others(29): Show |
37 | HG00280.hp1 HG00323.hp2 HG00639.hp2 others(34): Show |
intron_variant | MODIFIER | c.94+671delA | MFAP5 | ENSG00000197614.11 | transcript | ENST00000359478.7 | protein_coding | 3/9 | chr12 | 8660191 | |||||||
| chr12:8660292 | C | A | 4 | a0001c0001t0005g0034 a0001c0001t0009g0066 a0001c0001t0009g0067 others(1): Show |
5 | HG02723.hp2 HG03139.hp1 HG03834.hp2 others(2): Show |
intron_variant | MODIFIER | c.94+571G>T | MFAP5 | ENSG00000197614.11 | transcript | ENST00000359478.7 | protein_coding | 3/9 | chr12 | 8660292 | |||||||
| chr12:8660368 | C | A | 3 | a0001c0001t0003g0057 a0001c0001t0003g0206 a0001c0001t0012g0205 |
4 | HG02109.hp1 HG02572.hp2 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.94+495G>T | MFAP5 | ENSG00000197614.11 | transcript | ENST00000359478.7 | protein_coding | 3/9 | chr12 | 8660368 | |||||||
| chr12:8660497 | T | C | 3 | a0001c0001t0003g0057 a0001c0001t0003g0206 a0001c0001t0012g0205 |
4 | HG02109.hp1 HG02572.hp2 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.94+366A>G | MFAP5 | ENSG00000197614.11 | transcript | ENST00000359478.7 | protein_coding | 3/9 | chr12 | 8660497 | |||||||
| chr12:8660523 | C | T | 7 | a0001c0001t0003g0057 a0001c0001t0003g0206 a0001c0001t0005g0034 others(4): Show |
9 | HG02109.hp1 HG02572.hp2 HG02723.hp2 others(6): Show |
intron_variant | MODIFIER | c.94+340G>A | MFAP5 | ENSG00000197614.11 | transcript | ENST00000359478.7 | protein_coding | 3/9 | chr12 | 8660523 | |||||||
| chr12:8660584 | G | A | 3 | a0001c0001t0001g0055 a0001c0001t0001g0168 a0001c0001t0001g0169 |
4 | HG02055.hp2 HG02486.hp1 HG02486.hp2 others(1): Show |
intron_variant | MODIFIER | c.94+279C>T | MFAP5 | ENSG00000197614.11 | transcript | ENST00000359478.7 | protein_coding | 3/9 | chr12 | 8660584 | |||||||
| chr12:8660629 | T | C | 5 | a0001c0001t0006g0170 a0001c0001t0006g0171 a0001c0001t0006g0172 others(2): Show |
5 | HG02622.hp2 HG02809.hp2 HG02965.hp1 others(2): Show |
intron_variant | MODIFIER | c.94+234A>G | MFAP5 | ENSG00000197614.11 | transcript | ENST00000359478.7 | protein_coding | 3/9 | chr12 | 8660629 | |||||||
| chr12:8660694 | A | G | 9 | a0001c0001t0003g0056 a0001c0001t0003g0196 a0001c0001t0003g0197 others(6): Show |
11 | HG01168.hp2 HG01169.hp1 HG01261.hp1 others(8): Show |
intron_variant | MODIFIER | c.94+169T>C | MFAP5 | ENSG00000197614.11 | transcript | ENST00000359478.7 | protein_coding | 3/9 | chr12 | 8660694 | |||||||
| chr12:8660716 | T | C | 3 | a0001c0001t0003g0057 a0001c0001t0003g0206 a0001c0001t0012g0205 |
4 | HG02109.hp1 HG02572.hp2 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.94+147A>G | MFAP5 | ENSG00000197614.11 | transcript | ENST00000359478.7 | protein_coding | 3/9 | chr12 | 8660716 | |||||||
| chr12:8660749 | C | CT | 10 | a0001c0001t0001g0019 a0001c0001t0001g0036 a0001c0001t0001g0037 others(7): Show |
14 | HG01928.hp2 NA18946.hp1 NA18948.hp2 others(11): Show |
intron_variant | MODIFIER | c.94+113dupA | MFAP5 | ENSG00000197614.11 | transcript | ENST00000359478.7 | protein_coding | 3/9 | chr12 | 8660749 | |||||||
| chr12:8660749 | CT | C | 8 | a0001c0001t0001g0174 a0001c0001t0004g0018 a0001c0001t0004g0032 others(5): Show |
12 | HG00280.hp1 HG01123.hp1 HG01257.hp2 others(9): Show |
intron_variant | MODIFIER | c.94+113delA | MFAP5 | ENSG00000197614.11 | transcript | ENST00000359478.7 | protein_coding | 3/9 | chr12 | 8660749 | |||||||
| chr12:8660753 | T | C | 1 | a0001c0001t0011g0175 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.94+110A>G | MFAP5 | ENSG00000197614.11 | transcript | ENST00000359478.7 | protein_coding | 3/9 | chr12 | 8660753 | |||||||
| chr12:8660842 | G | A | 1 | a0001c0001t0002g0176 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.94+21C>T | MFAP5 | ENSG00000197614.11 | transcript | ENST00000359478.7 | protein_coding | 3/9 | chr12 | 8660842 | |||||||
| chr12:8660902 | T | A | 8 | a0001c0001t0004g0018 a0001c0001t0004g0032 a0001c0001t0004g0033 others(5): Show |
12 | HG00280.hp1 HG00323.hp2 HG01123.hp1 others(9): Show |
splice_region_variant&intron_variant | LOW | c.59-4A>T | MFAP5 | ENSG00000197614.11 | transcript | ENST00000359478.7 | protein_coding | 2/9 | chr12 | 8660902 | |||||||
| chr12:8660949 | C | T | 2 | a0001c0001t0001g0185 a0001c0001t0001g0186 |
2 | NA19074.hp1 NA19081.hp2 |
intron_variant | MODIFIER | c.59-51G>A | MFAP5 | ENSG00000197614.11 | transcript | ENST00000359478.7 | protein_coding | 2/9 | chr12 | 8660949 | |||||||
| chr12:8660999 | T | A | 8 | a0001c0001t0004g0018 a0001c0001t0004g0032 a0001c0001t0004g0033 others(5): Show |
12 | HG00280.hp1 HG00323.hp2 HG01123.hp1 others(9): Show |
intron_variant | MODIFIER | c.59-101A>T | MFAP5 | ENSG00000197614.11 | transcript | ENST00000359478.7 | protein_coding | 2/9 | chr12 | 8660999 | |||||||
| chr12:8661213 | C | T | 1 | a0001c0001t0001g0074 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.59-315G>A | MFAP5 | ENSG00000197614.11 | transcript | ENST00000359478.7 | protein_coding | 2/9 | chr12 | 8661213 | |||||||
| chr12:8661277 | G | A | 10 | a0001c0001t0001g0006 a0001c0001t0001g0030 a0001c0001t0001g0177 others(7): Show |
18 | HG02015.hp2 HG02040.hp1 HG02056.hp2 others(15): Show |
intron_variant | MODIFIER | c.59-379C>T | MFAP5 | ENSG00000197614.11 | transcript | ENST00000359478.7 | protein_coding | 2/9 | chr12 | 8661277 | |||||||
| chr12:8661304 | T | C | 14 | a0001c0001t0001g0008 a0001c0001t0001g0017 a0001c0001t0001g0031 others(11): Show |
23 | HG00544.hp2 HG00597.hp1 HG02080.hp1 others(20): Show |
intron_variant | MODIFIER | c.59-406A>G | MFAP5 | ENSG00000197614.11 | transcript | ENST00000359478.7 | protein_coding | 2/9 | chr12 | 8661304 | |||||||
| chr12:8661331 | A | C | 3 | a0001c0001t0001g0035 a0001c0001t0001g0072 a0001c0001t0001g0073 |
4 | HG00735.hp1 HG01192.hp1 HG01243.hp1 others(1): Show |
intron_variant | MODIFIER | c.59-433T>G | MFAP5 | ENSG00000197614.11 | transcript | ENST00000359478.7 | protein_coding | 2/9 | chr12 | 8661331 | |||||||
| chr12:8661723 | C | T | 10 | a0001c0001t0004g0018 a0001c0001t0004g0032 a0001c0001t0004g0033 others(7): Show |
14 | HG00280.hp1 HG00323.hp2 HG01123.hp1 others(11): Show |
intron_variant | MODIFIER | c.58+324G>A | MFAP5 | ENSG00000197614.11 | transcript | ENST00000359478.7 | protein_coding | 2/9 | chr12 | 8661723 | |||||||
| chr12:8661949 | C | T | 1 | a0001c0001t0005g0034 | 2 | HG02723.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.58+98G>A | MFAP5 | ENSG00000197614.11 | transcript | ENST00000359478.7 | protein_coding | 2/9 | chr12 | 8661949 | |||||||
| chr12:8662115 | G | A | 1 | a0001c0001t0001g0195 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.-2-9C>T | MFAP5 | ENSG00000197614.11 | transcript | ENST00000359478.7 | protein_coding | 1/9 | chr12 | 8662115 | |||||||
| chr12:8662145 | A | C | 1 | a0001c0001t0001g0071 | 1 | NA18980.hp1 | intron_variant | MODIFIER | c.-2-39T>G | MFAP5 | ENSG00000197614.11 | transcript | ENST00000359478.7 | protein_coding | 1/9 | chr12 | 8662145 | |||||||
| chr12:8662378 | G | A | 3 | a0001c0001t0003g0057 a0001c0001t0003g0206 a0001c0001t0012g0205 |
4 | HG02109.hp1 HG02572.hp2 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.-3+249C>T | MFAP5 | ENSG00000197614.11 | transcript | ENST00000359478.7 | protein_coding | 1/9 | chr12 | 8662378 | |||||||
| chr12:8662470 | G | T | 1 | a0001c0001t0007g0070 | 1 | HG01071.hp1 | intron_variant | MODIFIER | c.-3+157C>A | MFAP5 | ENSG00000197614.11 | transcript | ENST00000359478.7 | protein_coding | 1/9 | chr12 | 8662470 |