geneid | 55669 |
---|---|
ensemblid | ENSG00000171109.19 |
hgncid | 18262 |
symbol | MFN1 |
name | mitofusin 1 |
refseq_nuc | NM_033540.3 |
refseq_prot | NP_284941.2 |
ensembl_nuc | ENST00000471841.6 |
ensembl_prot | ENSP00000420617.1 |
mane_status | MANE Select |
chr | chr3 |
start | 179347709 |
end | 179394936 |
strand | + |
ver | v1.2 |
region | chr3:179347709-179394936 |
region5000 | chr3:179342709-179399936 |
regionname0 | MFN1_chr3_179347709_179394936 |
regionname5000 | MFN1_chr3_179342709_179399936 |
ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 1/1 | 741 | 397 | 92 | 77 | 170 | 12 | 44 | 135 | MFN1_chr3_179342709_179399936 | MFN1 | copy fasta | chr3 | 179342709 | 179399936 |
a0002 | 0/0 | 741 | 2 | 0 | 0 | 2 | 0 | 0 | 1 | MFN1_chr3_179342709_179399936 | MFN1 | copy fasta | chr3 | 179342709 | 179399936 |
a0003 | 0/0 | 741 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | MFN1_chr3_179342709_179399936 | MFN1 | copy fasta | chr3 | 179342709 | 179399936 |
a0004 | 0/0 | 741 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | MFN1_chr3_179342709_179399936 | MFN1 | copy fasta | chr3 | 179342709 | 179399936 |
a0005 | 0/0 | 741 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | MFN1_chr3_179342709_179399936 | MFN1 | copy fasta | chr3 | 179342709 | 179399936 |
chapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
c0001 | 1/1 | 2226 | 385 | 88 | 77 | 167 | 12 | 39 | MFN1_chr3_179342709_179399936 | MFN1 | copy fasta | chr3 | 179342709 | 179399936 |
c0002 | 0/0 | 2226 | 6 | 0 | 0 | 1 | 0 | 5 | MFN1_chr3_179342709_179399936 | MFN1 | copy fasta | chr3 | 179342709 | 179399936 |
c0003 | 0/0 | 2226 | 2 | 0 | 0 | 2 | 0 | 0 | MFN1_chr3_179342709_179399936 | MFN1 | copy fasta | chr3 | 179342709 | 179399936 |
c0004 | 0/0 | 2226 | 2 | 0 | 0 | 2 | 0 | 0 | MFN1_chr3_179342709_179399936 | MFN1 | copy fasta | chr3 | 179342709 | 179399936 |
c0005 | 0/0 | 2226 | 2 | 2 | 0 | 0 | 0 | 0 | MFN1_chr3_179342709_179399936 | MFN1 | copy fasta | chr3 | 179342709 | 179399936 |
c0006 | 0/0 | 2226 | 1 | 0 | 1 | 0 | 0 | 0 | MFN1_chr3_179342709_179399936 | MFN1 | copy fasta | chr3 | 179342709 | 179399936 |
c0007 | 0/0 | 2226 | 1 | 1 | 0 | 0 | 0 | 0 | MFN1_chr3_179342709_179399936 | MFN1 | copy fasta | chr3 | 179342709 | 179399936 |
c0008 | 0/0 | 2226 | 1 | 1 | 0 | 0 | 0 | 0 | MFN1_chr3_179342709_179399936 | MFN1 | copy fasta | chr3 | 179342709 | 179399936 |
c0009 | 0/0 | 2226 | 1 | 1 | 0 | 0 | 0 | 0 | MFN1_chr3_179342709_179399936 | MFN1 | copy fasta | chr3 | 179342709 | 179399936 |
c0010 | 0/0 | 2226 | 1 | 1 | 0 | 0 | 0 | 0 | MFN1_chr3_179342709_179399936 | MFN1 | copy fasta | chr3 | 179342709 | 179399936 |
thapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
t0001 | 1/1 | 2987 | 133 | 17 | 21 | 75 | 2 | 16 | MFN1_chr3_179342709_179399936 | MFN1 | copy fasta | chr3 | 179342709 | 179399936 |
t0002 | 0/0 | 2986 | 51 | 2 | 15 | 29 | 2 | 3 | MFN1_chr3_179342709_179399936 | MFN1 | copy fasta | chr3 | 179342709 | 179399936 |
t0003 | 0/0 | 2988 | 20 | 3 | 4 | 11 | 0 | 2 | MFN1_chr3_179342709_179399936 | MFN1 | copy fasta | chr3 | 179342709 | 179399936 |
t0004 | 0/0 | 2988 | 19 | 1 | 3 | 8 | 3 | 4 | MFN1_chr3_179342709_179399936 | MFN1 | copy fasta | chr3 | 179342709 | 179399936 |
t0005 | 0/0 | 2987 | 16 | 1 | 3 | 7 | 1 | 4 | MFN1_chr3_179342709_179399936 | MFN1 | copy fasta | chr3 | 179342709 | 179399936 |
t0006 | 0/0 | 2987 | 13 | 13 | 0 | 0 | 0 | 0 | MFN1_chr3_179342709_179399936 | MFN1 | copy fasta | chr3 | 179342709 | 179399936 |
t0007 | 0/0 | 2986 | 13 | 0 | 3 | 7 | 1 | 2 | MFN1_chr3_179342709_179399936 | MFN1 | copy fasta | chr3 | 179342709 | 179399936 |
t0008 | 0/0 | 2986 | 12 | 0 | 1 | 11 | 0 | 0 | MFN1_chr3_179342709_179399936 | MFN1 | copy fasta | chr3 | 179342709 | 179399936 |
t0009 | 0/0 | 2979 | 11 | 11 | 0 | 0 | 0 | 0 | MFN1_chr3_179342709_179399936 | MFN1 | copy fasta | chr3 | 179342709 | 179399936 |
t0010 | 0/0 | 2988 | 8 | 0 | 0 | 8 | 0 | 0 | MFN1_chr3_179342709_179399936 | MFN1 | copy fasta | chr3 | 179342709 | 179399936 |
t0011 | 0/0 | 2986 | 7 | 0 | 2 | 5 | 0 | 0 | MFN1_chr3_179342709_179399936 | MFN1 | copy fasta | chr3 | 179342709 | 179399936 |
t0012 | 0/0 | 2988 | 7 | 5 | 2 | 0 | 0 | 0 | MFN1_chr3_179342709_179399936 | MFN1 | copy fasta | chr3 | 179342709 | 179399936 |
t0013 | 0/0 | 2987 | 7 | 1 | 6 | 0 | 0 | 0 | MFN1_chr3_179342709_179399936 | MFN1 | copy fasta | chr3 | 179342709 | 179399936 |
t0014 | 0/0 | 2988 | 7 | 0 | 3 | 0 | 2 | 2 | MFN1_chr3_179342709_179399936 | MFN1 | copy fasta | chr3 | 179342709 | 179399936 |
t0015 | 0/0 | 2988 | 6 | 4 | 2 | 0 | 0 | 0 | MFN1_chr3_179342709_179399936 | MFN1 | copy fasta | chr3 | 179342709 | 179399936 |
t0016 | 0/0 | 2987 | 6 | 0 | 2 | 0 | 0 | 4 | MFN1_chr3_179342709_179399936 | MFN1 | copy fasta | chr3 | 179342709 | 179399936 |
t0017 | 0/0 | 2989 | 6 | 3 | 0 | 0 | 0 | 3 | MFN1_chr3_179342709_179399936 | MFN1 | copy fasta | chr3 | 179342709 | 179399936 |
t0018 | 0/0 | 2990 | 5 | 3 | 2 | 0 | 0 | 0 | MFN1_chr3_179342709_179399936 | MFN1 | copy fasta | chr3 | 179342709 | 179399936 |
t0019 | 0/0 | 2987 | 4 | 4 | 0 | 0 | 0 | 0 | MFN1_chr3_179342709_179399936 | MFN1 | copy fasta | chr3 | 179342709 | 179399936 |
t0020 | 0/0 | 2987 | 3 | 2 | 1 | 0 | 0 | 0 | MFN1_chr3_179342709_179399936 | MFN1 | copy fasta | chr3 | 179342709 | 179399936 |
t0021 | 0/0 | 2988 | 3 | 3 | 0 | 0 | 0 | 0 | MFN1_chr3_179342709_179399936 | MFN1 | copy fasta | chr3 | 179342709 | 179399936 |
t0022 | 0/0 | 2989 | 3 | 0 | 1 | 0 | 0 | 2 | MFN1_chr3_179342709_179399936 | MFN1 | copy fasta | chr3 | 179342709 | 179399936 |
t0023 | 0/0 | 2988 | 2 | 2 | 0 | 0 | 0 | 0 | MFN1_chr3_179342709_179399936 | MFN1 | copy fasta | chr3 | 179342709 | 179399936 |
t0024 | 0/0 | 2987 | 2 | 0 | 0 | 2 | 0 | 0 | MFN1_chr3_179342709_179399936 | MFN1 | copy fasta | chr3 | 179342709 | 179399936 |
t0025 | 0/0 | 2984 | 2 | 0 | 2 | 0 | 0 | 0 | MFN1_chr3_179342709_179399936 | MFN1 | copy fasta | chr3 | 179342709 | 179399936 |
t0026 | 0/0 | 2986 | 2 | 2 | 0 | 0 | 0 | 0 | MFN1_chr3_179342709_179399936 | MFN1 | copy fasta | chr3 | 179342709 | 179399936 |
t0027 | 0/0 | 2987 | 2 | 2 | 0 | 0 | 0 | 0 | MFN1_chr3_179342709_179399936 | MFN1 | copy fasta | chr3 | 179342709 | 179399936 |
t0028 | 0/0 | 2987 | 2 | 0 | 0 | 1 | 1 | 0 | MFN1_chr3_179342709_179399936 | MFN1 | copy fasta | chr3 | 179342709 | 179399936 |
t0029 | 0/0 | 2987 | 2 | 0 | 0 | 2 | 0 | 0 | MFN1_chr3_179342709_179399936 | MFN1 | copy fasta | chr3 | 179342709 | 179399936 |
t0030 | 0/0 | 2986 | 2 | 0 | 2 | 0 | 0 | 0 | MFN1_chr3_179342709_179399936 | MFN1 | copy fasta | chr3 | 179342709 | 179399936 |
t0031 | 0/0 | 2989 | 2 | 0 | 1 | 1 | 0 | 0 | MFN1_chr3_179342709_179399936 | MFN1 | copy fasta | chr3 | 179342709 | 179399936 |
t0032 | 0/0 | 2990 | 2 | 1 | 1 | 0 | 0 | 0 | MFN1_chr3_179342709_179399936 | MFN1 | copy fasta | chr3 | 179342709 | 179399936 |
t0033 | 0/0 | 2987 | 2 | 2 | 0 | 0 | 0 | 0 | MFN1_chr3_179342709_179399936 | MFN1 | copy fasta | chr3 | 179342709 | 179399936 |
t0034 | 0/0 | 2987 | 2 | 2 | 0 | 0 | 0 | 0 | MFN1_chr3_179342709_179399936 | MFN1 | copy fasta | chr3 | 179342709 | 179399936 |
t0035 | 0/0 | 2988 | 1 | 1 | 0 | 0 | 0 | 0 | MFN1_chr3_179342709_179399936 | MFN1 | copy fasta | chr3 | 179342709 | 179399936 |
t0036 | 0/0 | 2989 | 1 | 1 | 0 | 0 | 0 | 0 | MFN1_chr3_179342709_179399936 | MFN1 | copy fasta | chr3 | 179342709 | 179399936 |
t0037 | 0/0 | 2985 | 1 | 0 | 1 | 0 | 0 | 0 | MFN1_chr3_179342709_179399936 | MFN1 | copy fasta | chr3 | 179342709 | 179399936 |
t0038 | 0/0 | 2987 | 1 | 0 | 0 | 0 | 0 | 1 | MFN1_chr3_179342709_179399936 | MFN1 | copy fasta | chr3 | 179342709 | 179399936 |
t0039 | 0/0 | 2988 | 1 | 1 | 0 | 0 | 0 | 0 | MFN1_chr3_179342709_179399936 | MFN1 | copy fasta | chr3 | 179342709 | 179399936 |
t0040 | 0/0 | 2989 | 1 | 1 | 0 | 0 | 0 | 0 | MFN1_chr3_179342709_179399936 | MFN1 | copy fasta | chr3 | 179342709 | 179399936 |
t0041 | 0/0 | 2986 | 1 | 1 | 0 | 0 | 0 | 0 | MFN1_chr3_179342709_179399936 | MFN1 | copy fasta | chr3 | 179342709 | 179399936 |
t0042 | 0/0 | 2987 | 1 | 1 | 0 | 0 | 0 | 0 | MFN1_chr3_179342709_179399936 | MFN1 | copy fasta | chr3 | 179342709 | 179399936 |
t0043 | 0/0 | 2988 | 1 | 0 | 0 | 0 | 0 | 1 | MFN1_chr3_179342709_179399936 | MFN1 | copy fasta | chr3 | 179342709 | 179399936 |
t0044 | 0/0 | 2986 | 1 | 0 | 0 | 1 | 0 | 0 | MFN1_chr3_179342709_179399936 | MFN1 | copy fasta | chr3 | 179342709 | 179399936 |
t0045 | 0/0 | 2979 | 1 | 1 | 0 | 0 | 0 | 0 | MFN1_chr3_179342709_179399936 | MFN1 | copy fasta | chr3 | 179342709 | 179399936 |
t0046 | 0/0 | 2988 | 1 | 0 | 0 | 1 | 0 | 0 | MFN1_chr3_179342709_179399936 | MFN1 | copy fasta | chr3 | 179342709 | 179399936 |
t0047 | 0/0 | 2987 | 1 | 0 | 0 | 1 | 0 | 0 | MFN1_chr3_179342709_179399936 | MFN1 | copy fasta | chr3 | 179342709 | 179399936 |
t0048 | 0/0 | 2988 | 1 | 0 | 0 | 1 | 0 | 0 | MFN1_chr3_179342709_179399936 | MFN1 | copy fasta | chr3 | 179342709 | 179399936 |
t0049 | 0/0 | 2977 | 1 | 1 | 0 | 0 | 0 | 0 | MFN1_chr3_179342709_179399936 | MFN1 | copy fasta | chr3 | 179342709 | 179399936 |
t0050 | 0/0 | 2987 | 1 | 0 | 0 | 1 | 0 | 0 | MFN1_chr3_179342709_179399936 | MFN1 | copy fasta | chr3 | 179342709 | 179399936 |
t0051 | 0/0 | 2987 | 1 | 1 | 0 | 0 | 0 | 0 | MFN1_chr3_179342709_179399936 | MFN1 | copy fasta | chr3 | 179342709 | 179399936 |
t0052 | 0/0 | 2988 | 1 | 1 | 0 | 0 | 0 | 0 | MFN1_chr3_179342709_179399936 | MFN1 | copy fasta | chr3 | 179342709 | 179399936 |
ghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
g0001 | 0/0 | 10 | 0 | 1 | 8 | 1 | 0 | MFN1_chr3_179342709_179399936 | MFN1 | chr3 | 179342709 | 179399936 |
g0002 | 0/0 | 6 | 0 | 0 | 2 | 0 | 4 | MFN1_chr3_179342709_179399936 | MFN1 | chr3 | 179342709 | 179399936 |
g0003 | 0/0 | 6 | 0 | 0 | 6 | 0 | 0 | MFN1_chr3_179342709_179399936 | MFN1 | chr3 | 179342709 | 179399936 |
g0004 | 0/0 | 5 | 4 | 1 | 0 | 0 | 0 | MFN1_chr3_179342709_179399936 | MFN1 | chr3 | 179342709 | 179399936 |
g0005 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | MFN1_chr3_179342709_179399936 | MFN1 | chr3 | 179342709 | 179399936 |
g0006 | 0/0 | 5 | 0 | 2 | 1 | 0 | 2 | MFN1_chr3_179342709_179399936 | MFN1 | chr3 | 179342709 | 179399936 |
g0007 | 0/0 | 5 | 0 | 4 | 0 | 0 | 1 | MFN1_chr3_179342709_179399936 | MFN1 | chr3 | 179342709 | 179399936 |
g0008 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | MFN1_chr3_179342709_179399936 | MFN1 | chr3 | 179342709 | 179399936 |
g0009 | 0/0 | 5 | 5 | 0 | 0 | 0 | 0 | MFN1_chr3_179342709_179399936 | MFN1 | chr3 | 179342709 | 179399936 |
g0010 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | MFN1_chr3_179342709_179399936 | MFN1 | chr3 | 179342709 | 179399936 |
g0011 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | MFN1_chr3_179342709_179399936 | MFN1 | chr3 | 179342709 | 179399936 |
g0012 | 0/1 | 4 | 0 | 2 | 0 | 0 | 1 | MFN1_chr3_179342709_179399936 | MFN1 | chr3 | 179342709 | 179399936 |
g0013 | 0/0 | 4 | 0 | 4 | 0 | 0 | 0 | MFN1_chr3_179342709_179399936 | MFN1 | chr3 | 179342709 | 179399936 |
g0014 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | MFN1_chr3_179342709_179399936 | MFN1 | chr3 | 179342709 | 179399936 |
g0015 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | MFN1_chr3_179342709_179399936 | MFN1 | chr3 | 179342709 | 179399936 |
g0016 | 0/0 | 3 | 0 | 1 | 0 | 0 | 2 | MFN1_chr3_179342709_179399936 | MFN1 | chr3 | 179342709 | 179399936 |
g0017 | 0/0 | 3 | 0 | 1 | 1 | 0 | 1 | MFN1_chr3_179342709_179399936 | MFN1 | chr3 | 179342709 | 179399936 |
g0018 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | MFN1_chr3_179342709_179399936 | MFN1 | chr3 | 179342709 | 179399936 |
g0019 | 0/0 | 3 | 0 | 1 | 2 | 0 | 0 | MFN1_chr3_179342709_179399936 | MFN1 | chr3 | 179342709 | 179399936 |
g0020 | 0/0 | 3 | 2 | 1 | 0 | 0 | 0 | MFN1_chr3_179342709_179399936 | MFN1 | chr3 | 179342709 | 179399936 |
g0021 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | MFN1_chr3_179342709_179399936 | MFN1 | chr3 | 179342709 | 179399936 |
g0022 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | MFN1_chr3_179342709_179399936 | MFN1 | chr3 | 179342709 | 179399936 |
g0023 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MFN1_chr3_179342709_179399936 | MFN1 | chr3 | 179342709 | 179399936 |
g0024 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MFN1_chr3_179342709_179399936 | MFN1 | chr3 | 179342709 | 179399936 |
g0025 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MFN1_chr3_179342709_179399936 | MFN1 | chr3 | 179342709 | 179399936 |
g0026 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MFN1_chr3_179342709_179399936 | MFN1 | chr3 | 179342709 | 179399936 |
g0027 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MFN1_chr3_179342709_179399936 | MFN1 | chr3 | 179342709 | 179399936 |
g0028 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MFN1_chr3_179342709_179399936 | MFN1 | chr3 | 179342709 | 179399936 |
g0029 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MFN1_chr3_179342709_179399936 | MFN1 | chr3 | 179342709 | 179399936 |
g0030 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MFN1_chr3_179342709_179399936 | MFN1 | chr3 | 179342709 | 179399936 |
g0031 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MFN1_chr3_179342709_179399936 | MFN1 | chr3 | 179342709 | 179399936 |
g0032 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MFN1_chr3_179342709_179399936 | MFN1 | chr3 | 179342709 | 179399936 |
g0033 | 1/0 | 2 | 0 | 1 | 0 | 0 | 0 | MFN1_chr3_179342709_179399936 | MFN1 | chr3 | 179342709 | 179399936 |
g0034 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MFN1_chr3_179342709_179399936 | MFN1 | chr3 | 179342709 | 179399936 |
g0035 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | MFN1_chr3_179342709_179399936 | MFN1 | chr3 | 179342709 | 179399936 |
g0036 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MFN1_chr3_179342709_179399936 | MFN1 | chr3 | 179342709 | 179399936 |
g0037 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MFN1_chr3_179342709_179399936 | MFN1 | chr3 | 179342709 | 179399936 |
g0038 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | MFN1_chr3_179342709_179399936 | MFN1 | chr3 | 179342709 | 179399936 |
g0039 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MFN1_chr3_179342709_179399936 | MFN1 | chr3 | 179342709 | 179399936 |
g0040 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MFN1_chr3_179342709_179399936 | MFN1 | chr3 | 179342709 | 179399936 |
g0041 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MFN1_chr3_179342709_179399936 | MFN1 | chr3 | 179342709 | 179399936 |
g0042 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | MFN1_chr3_179342709_179399936 | MFN1 | chr3 | 179342709 | 179399936 |
g0043 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | MFN1_chr3_179342709_179399936 | MFN1 | chr3 | 179342709 | 179399936 |
g0044 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MFN1_chr3_179342709_179399936 | MFN1 | chr3 | 179342709 | 179399936 |
g0045 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MFN1_chr3_179342709_179399936 | MFN1 | chr3 | 179342709 | 179399936 |
g0046 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | MFN1_chr3_179342709_179399936 | MFN1 | chr3 | 179342709 | 179399936 |
g0047 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MFN1_chr3_179342709_179399936 | MFN1 | chr3 | 179342709 | 179399936 |
g0048 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MFN1_chr3_179342709_179399936 | MFN1 | chr3 | 179342709 | 179399936 |
g0049 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MFN1_chr3_179342709_179399936 | MFN1 | chr3 | 179342709 | 179399936 |
g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFN1_chr3_179342709_179399936 | MFN1 | chr3 | 179342709 | 179399936 |
g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFN1_chr3_179342709_179399936 | MFN1 | chr3 | 179342709 | 179399936 |
g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFN1_chr3_179342709_179399936 | MFN1 | chr3 | 179342709 | 179399936 |
g0053 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MFN1_chr3_179342709_179399936 | MFN1 | chr3 | 179342709 | 179399936 |
g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFN1_chr3_179342709_179399936 | MFN1 | chr3 | 179342709 | 179399936 |
g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFN1_chr3_179342709_179399936 | MFN1 | chr3 | 179342709 | 179399936 |
g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFN1_chr3_179342709_179399936 | MFN1 | chr3 | 179342709 | 179399936 |
g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFN1_chr3_179342709_179399936 | MFN1 | chr3 | 179342709 | 179399936 |
g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFN1_chr3_179342709_179399936 | MFN1 | chr3 | 179342709 | 179399936 |
g0059 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MFN1_chr3_179342709_179399936 | MFN1 | chr3 | 179342709 | 179399936 |
g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFN1_chr3_179342709_179399936 | MFN1 | chr3 | 179342709 | 179399936 |
g0061 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MFN1_chr3_179342709_179399936 | MFN1 | chr3 | 179342709 | 179399936 |
g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFN1_chr3_179342709_179399936 | MFN1 | chr3 | 179342709 | 179399936 |
g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFN1_chr3_179342709_179399936 | MFN1 | chr3 | 179342709 | 179399936 |
g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFN1_chr3_179342709_179399936 | MFN1 | chr3 | 179342709 | 179399936 |
g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFN1_chr3_179342709_179399936 | MFN1 | chr3 | 179342709 | 179399936 |
g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFN1_chr3_179342709_179399936 | MFN1 | chr3 | 179342709 | 179399936 |
g0067 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MFN1_chr3_179342709_179399936 | MFN1 | chr3 | 179342709 | 179399936 |
g0068 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MFN1_chr3_179342709_179399936 | MFN1 | chr3 | 179342709 | 179399936 |
g0069 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MFN1_chr3_179342709_179399936 | MFN1 | chr3 | 179342709 | 179399936 |
g0070 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MFN1_chr3_179342709_179399936 | MFN1 | chr3 | 179342709 | 179399936 |
g0071 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MFN1_chr3_179342709_179399936 | MFN1 | chr3 | 179342709 | 179399936 |
g0072 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MFN1_chr3_179342709_179399936 | MFN1 | chr3 | 179342709 | 179399936 |
g0073 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MFN1_chr3_179342709_179399936 | MFN1 | chr3 | 179342709 | 179399936 |
g0074 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MFN1_chr3_179342709_179399936 | MFN1 | chr3 | 179342709 | 179399936 |
g0075 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MFN1_chr3_179342709_179399936 | MFN1 | chr3 | 179342709 | 179399936 |
g0076 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MFN1_chr3_179342709_179399936 | MFN1 | chr3 | 179342709 | 179399936 |
g0077 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MFN1_chr3_179342709_179399936 | MFN1 | chr3 | 179342709 | 179399936 |
g0078 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MFN1_chr3_179342709_179399936 | MFN1 | chr3 | 179342709 | 179399936 |
g0079 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MFN1_chr3_179342709_179399936 | MFN1 | chr3 | 179342709 | 179399936 |
g0080 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MFN1_chr3_179342709_179399936 | MFN1 | chr3 | 179342709 | 179399936 |
g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFN1_chr3_179342709_179399936 | MFN1 | chr3 | 179342709 | 179399936 |
g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MFN1_chr3_179342709_179399936 | MFN1 | chr3 | 179342709 | 179399936 |
g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFN1_chr3_179342709_179399936 | MFN1 | chr3 | 179342709 | 179399936 |
g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFN1_chr3_179342709_179399936 | MFN1 | chr3 | 179342709 | 179399936 |
g0085 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MFN1_chr3_179342709_179399936 | MFN1 | chr3 | 179342709 | 179399936 |
g0086 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MFN1_chr3_179342709_179399936 | MFN1 | chr3 | 179342709 | 179399936 |
g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFN1_chr3_179342709_179399936 | MFN1 | chr3 | 179342709 | 179399936 |
g0088 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MFN1_chr3_179342709_179399936 | MFN1 | chr3 | 179342709 | 179399936 |
g0089 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MFN1_chr3_179342709_179399936 | MFN1 | chr3 | 179342709 | 179399936 |
g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFN1_chr3_179342709_179399936 | MFN1 | chr3 | 179342709 | 179399936 |
g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFN1_chr3_179342709_179399936 | MFN1 | chr3 | 179342709 | 179399936 |
g0092 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MFN1_chr3_179342709_179399936 | MFN1 | chr3 | 179342709 | 179399936 |
g0093 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MFN1_chr3_179342709_179399936 | MFN1 | chr3 | 179342709 | 179399936 |
g0094 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MFN1_chr3_179342709_179399936 | MFN1 | chr3 | 179342709 | 179399936 |
g0095 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MFN1_chr3_179342709_179399936 | MFN1 | chr3 | 179342709 | 179399936 |
g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MFN1_chr3_179342709_179399936 | MFN1 | chr3 | 179342709 | 179399936 |
g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFN1_chr3_179342709_179399936 | MFN1 | chr3 | 179342709 | 179399936 |
g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFN1_chr3_179342709_179399936 | MFN1 | chr3 | 179342709 | 179399936 |
g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFN1_chr3_179342709_179399936 | MFN1 | chr3 | 179342709 | 179399936 |
g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFN1_chr3_179342709_179399936 | MFN1 | chr3 | 179342709 | 179399936 |
g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MFN1_chr3_179342709_179399936 | MFN1 | chr3 | 179342709 | 179399936 |
g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFN1_chr3_179342709_179399936 | MFN1 | chr3 | 179342709 | 179399936 |
g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFN1_chr3_179342709_179399936 | MFN1 | chr3 | 179342709 | 179399936 |
g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFN1_chr3_179342709_179399936 | MFN1 | chr3 | 179342709 | 179399936 |
g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFN1_chr3_179342709_179399936 | MFN1 | chr3 | 179342709 | 179399936 |
g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFN1_chr3_179342709_179399936 | MFN1 | chr3 | 179342709 | 179399936 |
g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFN1_chr3_179342709_179399936 | MFN1 | chr3 | 179342709 | 179399936 |
g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFN1_chr3_179342709_179399936 | MFN1 | chr3 | 179342709 | 179399936 |
g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFN1_chr3_179342709_179399936 | MFN1 | chr3 | 179342709 | 179399936 |
g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFN1_chr3_179342709_179399936 | MFN1 | chr3 | 179342709 | 179399936 |
g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFN1_chr3_179342709_179399936 | MFN1 | chr3 | 179342709 | 179399936 |
g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFN1_chr3_179342709_179399936 | MFN1 | chr3 | 179342709 | 179399936 |
g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFN1_chr3_179342709_179399936 | MFN1 | chr3 | 179342709 | 179399936 |
g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFN1_chr3_179342709_179399936 | MFN1 | chr3 | 179342709 | 179399936 |
g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFN1_chr3_179342709_179399936 | MFN1 | chr3 | 179342709 | 179399936 |
g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFN1_chr3_179342709_179399936 | MFN1 | chr3 | 179342709 | 179399936 |
g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFN1_chr3_179342709_179399936 | MFN1 | chr3 | 179342709 | 179399936 |
g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFN1_chr3_179342709_179399936 | MFN1 | chr3 | 179342709 | 179399936 |
g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFN1_chr3_179342709_179399936 | MFN1 | chr3 | 179342709 | 179399936 |
g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFN1_chr3_179342709_179399936 | MFN1 | chr3 | 179342709 | 179399936 |
g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFN1_chr3_179342709_179399936 | MFN1 | chr3 | 179342709 | 179399936 |
g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFN1_chr3_179342709_179399936 | MFN1 | chr3 | 179342709 | 179399936 |
g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFN1_chr3_179342709_179399936 | MFN1 | chr3 | 179342709 | 179399936 |
g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFN1_chr3_179342709_179399936 | MFN1 | chr3 | 179342709 | 179399936 |
g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFN1_chr3_179342709_179399936 | MFN1 | chr3 | 179342709 | 179399936 |
g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFN1_chr3_179342709_179399936 | MFN1 | chr3 | 179342709 | 179399936 |
g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFN1_chr3_179342709_179399936 | MFN1 | chr3 | 179342709 | 179399936 |
g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFN1_chr3_179342709_179399936 | MFN1 | chr3 | 179342709 | 179399936 |
g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFN1_chr3_179342709_179399936 | MFN1 | chr3 | 179342709 | 179399936 |
g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFN1_chr3_179342709_179399936 | MFN1 | chr3 | 179342709 | 179399936 |
g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFN1_chr3_179342709_179399936 | MFN1 | chr3 | 179342709 | 179399936 |
g0132 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MFN1_chr3_179342709_179399936 | MFN1 | chr3 | 179342709 | 179399936 |
g0133 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MFN1_chr3_179342709_179399936 | MFN1 | chr3 | 179342709 | 179399936 |
g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFN1_chr3_179342709_179399936 | MFN1 | chr3 | 179342709 | 179399936 |
g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFN1_chr3_179342709_179399936 | MFN1 | chr3 | 179342709 | 179399936 |
g0136 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MFN1_chr3_179342709_179399936 | MFN1 | chr3 | 179342709 | 179399936 |
g0137 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MFN1_chr3_179342709_179399936 | MFN1 | chr3 | 179342709 | 179399936 |
g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFN1_chr3_179342709_179399936 | MFN1 | chr3 | 179342709 | 179399936 |
g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFN1_chr3_179342709_179399936 | MFN1 | chr3 | 179342709 | 179399936 |
g0140 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MFN1_chr3_179342709_179399936 | MFN1 | chr3 | 179342709 | 179399936 |
g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFN1_chr3_179342709_179399936 | MFN1 | chr3 | 179342709 | 179399936 |
g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFN1_chr3_179342709_179399936 | MFN1 | chr3 | 179342709 | 179399936 |
g0143 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MFN1_chr3_179342709_179399936 | MFN1 | chr3 | 179342709 | 179399936 |
g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFN1_chr3_179342709_179399936 | MFN1 | chr3 | 179342709 | 179399936 |
g0145 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MFN1_chr3_179342709_179399936 | MFN1 | chr3 | 179342709 | 179399936 |
g0146 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MFN1_chr3_179342709_179399936 | MFN1 | chr3 | 179342709 | 179399936 |
g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFN1_chr3_179342709_179399936 | MFN1 | chr3 | 179342709 | 179399936 |
g0148 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MFN1_chr3_179342709_179399936 | MFN1 | chr3 | 179342709 | 179399936 |
g0149 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MFN1_chr3_179342709_179399936 | MFN1 | chr3 | 179342709 | 179399936 |
g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFN1_chr3_179342709_179399936 | MFN1 | chr3 | 179342709 | 179399936 |
g0151 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MFN1_chr3_179342709_179399936 | MFN1 | chr3 | 179342709 | 179399936 |
g0152 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MFN1_chr3_179342709_179399936 | MFN1 | chr3 | 179342709 | 179399936 |
g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFN1_chr3_179342709_179399936 | MFN1 | chr3 | 179342709 | 179399936 |
g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFN1_chr3_179342709_179399936 | MFN1 | chr3 | 179342709 | 179399936 |
g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFN1_chr3_179342709_179399936 | MFN1 | chr3 | 179342709 | 179399936 |
g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFN1_chr3_179342709_179399936 | MFN1 | chr3 | 179342709 | 179399936 |
g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFN1_chr3_179342709_179399936 | MFN1 | chr3 | 179342709 | 179399936 |
g0158 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MFN1_chr3_179342709_179399936 | MFN1 | chr3 | 179342709 | 179399936 |
g0159 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MFN1_chr3_179342709_179399936 | MFN1 | chr3 | 179342709 | 179399936 |
g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFN1_chr3_179342709_179399936 | MFN1 | chr3 | 179342709 | 179399936 |
g0161 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MFN1_chr3_179342709_179399936 | MFN1 | chr3 | 179342709 | 179399936 |
g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFN1_chr3_179342709_179399936 | MFN1 | chr3 | 179342709 | 179399936 |
g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFN1_chr3_179342709_179399936 | MFN1 | chr3 | 179342709 | 179399936 |
g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFN1_chr3_179342709_179399936 | MFN1 | chr3 | 179342709 | 179399936 |
g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFN1_chr3_179342709_179399936 | MFN1 | chr3 | 179342709 | 179399936 |
g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFN1_chr3_179342709_179399936 | MFN1 | chr3 | 179342709 | 179399936 |
g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFN1_chr3_179342709_179399936 | MFN1 | chr3 | 179342709 | 179399936 |
g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFN1_chr3_179342709_179399936 | MFN1 | chr3 | 179342709 | 179399936 |
g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFN1_chr3_179342709_179399936 | MFN1 | chr3 | 179342709 | 179399936 |
g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFN1_chr3_179342709_179399936 | MFN1 | chr3 | 179342709 | 179399936 |
g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFN1_chr3_179342709_179399936 | MFN1 | chr3 | 179342709 | 179399936 |
g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFN1_chr3_179342709_179399936 | MFN1 | chr3 | 179342709 | 179399936 |
g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFN1_chr3_179342709_179399936 | MFN1 | chr3 | 179342709 | 179399936 |
g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFN1_chr3_179342709_179399936 | MFN1 | chr3 | 179342709 | 179399936 |
g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFN1_chr3_179342709_179399936 | MFN1 | chr3 | 179342709 | 179399936 |
g0176 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MFN1_chr3_179342709_179399936 | MFN1 | chr3 | 179342709 | 179399936 |
g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFN1_chr3_179342709_179399936 | MFN1 | chr3 | 179342709 | 179399936 |
g0178 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MFN1_chr3_179342709_179399936 | MFN1 | chr3 | 179342709 | 179399936 |
g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFN1_chr3_179342709_179399936 | MFN1 | chr3 | 179342709 | 179399936 |
g0180 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MFN1_chr3_179342709_179399936 | MFN1 | chr3 | 179342709 | 179399936 |
g0181 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MFN1_chr3_179342709_179399936 | MFN1 | chr3 | 179342709 | 179399936 |
g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFN1_chr3_179342709_179399936 | MFN1 | chr3 | 179342709 | 179399936 |
g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFN1_chr3_179342709_179399936 | MFN1 | chr3 | 179342709 | 179399936 |
g0184 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MFN1_chr3_179342709_179399936 | MFN1 | chr3 | 179342709 | 179399936 |
g0185 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MFN1_chr3_179342709_179399936 | MFN1 | chr3 | 179342709 | 179399936 |
g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFN1_chr3_179342709_179399936 | MFN1 | chr3 | 179342709 | 179399936 |
g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFN1_chr3_179342709_179399936 | MFN1 | chr3 | 179342709 | 179399936 |
g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFN1_chr3_179342709_179399936 | MFN1 | chr3 | 179342709 | 179399936 |
g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFN1_chr3_179342709_179399936 | MFN1 | chr3 | 179342709 | 179399936 |
g0190 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MFN1_chr3_179342709_179399936 | MFN1 | chr3 | 179342709 | 179399936 |
g0191 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MFN1_chr3_179342709_179399936 | MFN1 | chr3 | 179342709 | 179399936 |
g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFN1_chr3_179342709_179399936 | MFN1 | chr3 | 179342709 | 179399936 |
g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFN1_chr3_179342709_179399936 | MFN1 | chr3 | 179342709 | 179399936 |
g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFN1_chr3_179342709_179399936 | MFN1 | chr3 | 179342709 | 179399936 |
g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFN1_chr3_179342709_179399936 | MFN1 | chr3 | 179342709 | 179399936 |
g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFN1_chr3_179342709_179399936 | MFN1 | chr3 | 179342709 | 179399936 |
g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFN1_chr3_179342709_179399936 | MFN1 | chr3 | 179342709 | 179399936 |
g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFN1_chr3_179342709_179399936 | MFN1 | chr3 | 179342709 | 179399936 |
g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFN1_chr3_179342709_179399936 | MFN1 | chr3 | 179342709 | 179399936 |
g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFN1_chr3_179342709_179399936 | MFN1 | chr3 | 179342709 | 179399936 |
g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFN1_chr3_179342709_179399936 | MFN1 | chr3 | 179342709 | 179399936 |
g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFN1_chr3_179342709_179399936 | MFN1 | chr3 | 179342709 | 179399936 |
g0203 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MFN1_chr3_179342709_179399936 | MFN1 | chr3 | 179342709 | 179399936 |
g0204 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MFN1_chr3_179342709_179399936 | MFN1 | chr3 | 179342709 | 179399936 |
g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFN1_chr3_179342709_179399936 | MFN1 | chr3 | 179342709 | 179399936 |
g0206 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MFN1_chr3_179342709_179399936 | MFN1 | chr3 | 179342709 | 179399936 |
g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFN1_chr3_179342709_179399936 | MFN1 | chr3 | 179342709 | 179399936 |
g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFN1_chr3_179342709_179399936 | MFN1 | chr3 | 179342709 | 179399936 |
g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFN1_chr3_179342709_179399936 | MFN1 | chr3 | 179342709 | 179399936 |
g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFN1_chr3_179342709_179399936 | MFN1 | chr3 | 179342709 | 179399936 |
g0211 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MFN1_chr3_179342709_179399936 | MFN1 | chr3 | 179342709 | 179399936 |
g0212 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MFN1_chr3_179342709_179399936 | MFN1 | chr3 | 179342709 | 179399936 |
g0213 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MFN1_chr3_179342709_179399936 | MFN1 | chr3 | 179342709 | 179399936 |
g0214 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MFN1_chr3_179342709_179399936 | MFN1 | chr3 | 179342709 | 179399936 |
g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFN1_chr3_179342709_179399936 | MFN1 | chr3 | 179342709 | 179399936 |
g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFN1_chr3_179342709_179399936 | MFN1 | chr3 | 179342709 | 179399936 |
g0217 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MFN1_chr3_179342709_179399936 | MFN1 | chr3 | 179342709 | 179399936 |
g0218 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MFN1_chr3_179342709_179399936 | MFN1 | chr3 | 179342709 | 179399936 |
g0219 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MFN1_chr3_179342709_179399936 | MFN1 | chr3 | 179342709 | 179399936 |
g0220 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MFN1_chr3_179342709_179399936 | MFN1 | chr3 | 179342709 | 179399936 |
g0221 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MFN1_chr3_179342709_179399936 | MFN1 | chr3 | 179342709 | 179399936 |
g0222 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MFN1_chr3_179342709_179399936 | MFN1 | chr3 | 179342709 | 179399936 |
g0223 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MFN1_chr3_179342709_179399936 | MFN1 | chr3 | 179342709 | 179399936 |
g0224 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MFN1_chr3_179342709_179399936 | MFN1 | chr3 | 179342709 | 179399936 |
g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFN1_chr3_179342709_179399936 | MFN1 | chr3 | 179342709 | 179399936 |
g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFN1_chr3_179342709_179399936 | MFN1 | chr3 | 179342709 | 179399936 |
g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFN1_chr3_179342709_179399936 | MFN1 | chr3 | 179342709 | 179399936 |
g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFN1_chr3_179342709_179399936 | MFN1 | chr3 | 179342709 | 179399936 |
g0229 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MFN1_chr3_179342709_179399936 | MFN1 | chr3 | 179342709 | 179399936 |
g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFN1_chr3_179342709_179399936 | MFN1 | chr3 | 179342709 | 179399936 |
g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFN1_chr3_179342709_179399936 | MFN1 | chr3 | 179342709 | 179399936 |
g0232 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MFN1_chr3_179342709_179399936 | MFN1 | chr3 | 179342709 | 179399936 |
g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFN1_chr3_179342709_179399936 | MFN1 | chr3 | 179342709 | 179399936 |
g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFN1_chr3_179342709_179399936 | MFN1 | chr3 | 179342709 | 179399936 |
g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFN1_chr3_179342709_179399936 | MFN1 | chr3 | 179342709 | 179399936 |
g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFN1_chr3_179342709_179399936 | MFN1 | chr3 | 179342709 | 179399936 |
g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFN1_chr3_179342709_179399936 | MFN1 | chr3 | 179342709 | 179399936 |
g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFN1_chr3_179342709_179399936 | MFN1 | chr3 | 179342709 | 179399936 |
g0239 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MFN1_chr3_179342709_179399936 | MFN1 | chr3 | 179342709 | 179399936 |
g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFN1_chr3_179342709_179399936 | MFN1 | chr3 | 179342709 | 179399936 |
g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFN1_chr3_179342709_179399936 | MFN1 | chr3 | 179342709 | 179399936 |
g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFN1_chr3_179342709_179399936 | MFN1 | chr3 | 179342709 | 179399936 |
g0243 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MFN1_chr3_179342709_179399936 | MFN1 | chr3 | 179342709 | 179399936 |
g0244 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MFN1_chr3_179342709_179399936 | MFN1 | chr3 | 179342709 | 179399936 |
g0245 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MFN1_chr3_179342709_179399936 | MFN1 | chr3 | 179342709 | 179399936 |
g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFN1_chr3_179342709_179399936 | MFN1 | chr3 | 179342709 | 179399936 |
g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFN1_chr3_179342709_179399936 | MFN1 | chr3 | 179342709 | 179399936 |
g0248 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MFN1_chr3_179342709_179399936 | MFN1 | chr3 | 179342709 | 179399936 |
g0249 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFN1_chr3_179342709_179399936 | MFN1 | chr3 | 179342709 | 179399936 |
g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFN1_chr3_179342709_179399936 | MFN1 | chr3 | 179342709 | 179399936 |
g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFN1_chr3_179342709_179399936 | MFN1 | chr3 | 179342709 | 179399936 |
g0252 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFN1_chr3_179342709_179399936 | MFN1 | chr3 | 179342709 | 179399936 |
g0253 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MFN1_chr3_179342709_179399936 | MFN1 | chr3 | 179342709 | 179399936 |
g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFN1_chr3_179342709_179399936 | MFN1 | chr3 | 179342709 | 179399936 |
g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFN1_chr3_179342709_179399936 | MFN1 | chr3 | 179342709 | 179399936 |
g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFN1_chr3_179342709_179399936 | MFN1 | chr3 | 179342709 | 179399936 |
g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFN1_chr3_179342709_179399936 | MFN1 | chr3 | 179342709 | 179399936 |
g0258 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MFN1_chr3_179342709_179399936 | MFN1 | chr3 | 179342709 | 179399936 |
g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFN1_chr3_179342709_179399936 | MFN1 | chr3 | 179342709 | 179399936 |
g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFN1_chr3_179342709_179399936 | MFN1 | chr3 | 179342709 | 179399936 |
g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFN1_chr3_179342709_179399936 | MFN1 | chr3 | 179342709 | 179399936 |
g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFN1_chr3_179342709_179399936 | MFN1 | chr3 | 179342709 | 179399936 |
g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFN1_chr3_179342709_179399936 | MFN1 | chr3 | 179342709 | 179399936 |
g0264 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MFN1_chr3_179342709_179399936 | MFN1 | chr3 | 179342709 | 179399936 |
g0265 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MFN1_chr3_179342709_179399936 | MFN1 | chr3 | 179342709 | 179399936 |
g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFN1_chr3_179342709_179399936 | MFN1 | chr3 | 179342709 | 179399936 |
g0267 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MFN1_chr3_179342709_179399936 | MFN1 | chr3 | 179342709 | 179399936 |
g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFN1_chr3_179342709_179399936 | MFN1 | chr3 | 179342709 | 179399936 |
g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFN1_chr3_179342709_179399936 | MFN1 | chr3 | 179342709 | 179399936 |
g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFN1_chr3_179342709_179399936 | MFN1 | chr3 | 179342709 | 179399936 |
g0271 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFN1_chr3_179342709_179399936 | MFN1 | chr3 | 179342709 | 179399936 |
g0272 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFN1_chr3_179342709_179399936 | MFN1 | chr3 | 179342709 | 179399936 |
g0273 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFN1_chr3_179342709_179399936 | MFN1 | chr3 | 179342709 | 179399936 |
g0274 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MFN1_chr3_179342709_179399936 | MFN1 | chr3 | 179342709 | 179399936 |
g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFN1_chr3_179342709_179399936 | MFN1 | chr3 | 179342709 | 179399936 |
g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFN1_chr3_179342709_179399936 | MFN1 | chr3 | 179342709 | 179399936 |
g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFN1_chr3_179342709_179399936 | MFN1 | chr3 | 179342709 | 179399936 |
g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFN1_chr3_179342709_179399936 | MFN1 | chr3 | 179342709 | 179399936 |
g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFN1_chr3_179342709_179399936 | MFN1 | chr3 | 179342709 | 179399936 |
g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFN1_chr3_179342709_179399936 | MFN1 | chr3 | 179342709 | 179399936 |
g0281 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MFN1_chr3_179342709_179399936 | MFN1 | chr3 | 179342709 | 179399936 |
g0282 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MFN1_chr3_179342709_179399936 | MFN1 | chr3 | 179342709 | 179399936 |
g0283 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MFN1_chr3_179342709_179399936 | MFN1 | chr3 | 179342709 | 179399936 |
g0284 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MFN1_chr3_179342709_179399936 | MFN1 | chr3 | 179342709 | 179399936 |
g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFN1_chr3_179342709_179399936 | MFN1 | chr3 | 179342709 | 179399936 |
g0286 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MFN1_chr3_179342709_179399936 | MFN1 | chr3 | 179342709 | 179399936 |
g0287 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFN1_chr3_179342709_179399936 | MFN1 | chr3 | 179342709 | 179399936 |
g0288 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFN1_chr3_179342709_179399936 | MFN1 | chr3 | 179342709 | 179399936 |
g0289 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFN1_chr3_179342709_179399936 | MFN1 | chr3 | 179342709 | 179399936 |
g0290 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFN1_chr3_179342709_179399936 | MFN1 | chr3 | 179342709 | 179399936 |
g0291 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MFN1_chr3_179342709_179399936 | MFN1 | chr3 | 179342709 | 179399936 |
g0292 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFN1_chr3_179342709_179399936 | MFN1 | chr3 | 179342709 | 179399936 |
g0293 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MFN1_chr3_179342709_179399936 | MFN1 | chr3 | 179342709 | 179399936 |
g0294 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MFN1_chr3_179342709_179399936 | MFN1 | chr3 | 179342709 | 179399936 |
g0295 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFN1_chr3_179342709_179399936 | MFN1 | chr3 | 179342709 | 179399936 |
g0296 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFN1_chr3_179342709_179399936 | MFN1 | chr3 | 179342709 | 179399936 |
g0297 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFN1_chr3_179342709_179399936 | MFN1 | chr3 | 179342709 | 179399936 |
g0298 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFN1_chr3_179342709_179399936 | MFN1 | chr3 | 179342709 | 179399936 |
g0299 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MFN1_chr3_179342709_179399936 | MFN1 | chr3 | 179342709 | 179399936 |
g0300 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MFN1_chr3_179342709_179399936 | MFN1 | chr3 | 179342709 | 179399936 |
g0301 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFN1_chr3_179342709_179399936 | MFN1 | chr3 | 179342709 | 179399936 |
g0302 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFN1_chr3_179342709_179399936 | MFN1 | chr3 | 179342709 | 179399936 |
g0303 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFN1_chr3_179342709_179399936 | MFN1 | chr3 | 179342709 | 179399936 |
g0304 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFN1_chr3_179342709_179399936 | MFN1 | chr3 | 179342709 | 179399936 |
achapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 1/1 | 2226 | 385 | 88 | 77 | 167 | 12 | 39 | MFN1_chr3_179342709_179399936 | MFN1 | copy fasta | chr3 | 179342709 | 179399936 |
a0001c0002 | 0/0 | 2226 | 6 | 0 | 0 | 1 | 0 | 5 | MFN1_chr3_179342709_179399936 | MFN1 | copy fasta | chr3 | 179342709 | 179399936 |
a0001c0004 | 0/0 | 2226 | 2 | 0 | 0 | 2 | 0 | 0 | MFN1_chr3_179342709_179399936 | MFN1 | copy fasta | chr3 | 179342709 | 179399936 |
a0001c0005 | 0/0 | 2226 | 2 | 2 | 0 | 0 | 0 | 0 | MFN1_chr3_179342709_179399936 | MFN1 | copy fasta | chr3 | 179342709 | 179399936 |
a0001c0008 | 0/0 | 2226 | 1 | 1 | 0 | 0 | 0 | 0 | MFN1_chr3_179342709_179399936 | MFN1 | copy fasta | chr3 | 179342709 | 179399936 |
a0001c0009 | 0/0 | 2226 | 1 | 1 | 0 | 0 | 0 | 0 | MFN1_chr3_179342709_179399936 | MFN1 | copy fasta | chr3 | 179342709 | 179399936 |
a0002c0003 | 0/0 | 2226 | 2 | 0 | 0 | 2 | 0 | 0 | MFN1_chr3_179342709_179399936 | MFN1 | copy fasta | chr3 | 179342709 | 179399936 |
a0003c0006 | 0/0 | 2226 | 1 | 0 | 1 | 0 | 0 | 0 | MFN1_chr3_179342709_179399936 | MFN1 | copy fasta | chr3 | 179342709 | 179399936 |
a0004c0007 | 0/0 | 2226 | 1 | 1 | 0 | 0 | 0 | 0 | MFN1_chr3_179342709_179399936 | MFN1 | copy fasta | chr3 | 179342709 | 179399936 |
a0005c0010 | 0/0 | 2226 | 1 | 1 | 0 | 0 | 0 | 0 | MFN1_chr3_179342709_179399936 | MFN1 | copy fasta | chr3 | 179342709 | 179399936 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 1/1 | 5212 | 132 | 17 | 21 | 74 | 2 | 16 | MFN1_chr3_179342709_179399936 | MFN1 | copy fasta | chr3 | 179342709 | 179399936 |
a0001c0001t0002 | 0/0 | 5211 | 49 | 2 | 15 | 27 | 2 | 3 | MFN1_chr3_179342709_179399936 | MFN1 | copy fasta | chr3 | 179342709 | 179399936 |
a0001c0001t0003 | 0/0 | 5213 | 18 | 3 | 3 | 10 | 0 | 2 | MFN1_chr3_179342709_179399936 | MFN1 | copy fasta | chr3 | 179342709 | 179399936 |
a0001c0001t0004 | 0/0 | 5213 | 17 | 1 | 3 | 7 | 3 | 3 | MFN1_chr3_179342709_179399936 | MFN1 | copy fasta | chr3 | 179342709 | 179399936 |
a0001c0001t0005 | 0/0 | 5212 | 16 | 1 | 3 | 7 | 1 | 4 | MFN1_chr3_179342709_179399936 | MFN1 | copy fasta | chr3 | 179342709 | 179399936 |
a0001c0001t0006 | 0/0 | 5212 | 13 | 13 | 0 | 0 | 0 | 0 | MFN1_chr3_179342709_179399936 | MFN1 | copy fasta | chr3 | 179342709 | 179399936 |
a0001c0001t0007 | 0/0 | 5211 | 13 | 0 | 3 | 7 | 1 | 2 | MFN1_chr3_179342709_179399936 | MFN1 | copy fasta | chr3 | 179342709 | 179399936 |
a0001c0001t0008 | 0/0 | 5211 | 12 | 0 | 1 | 11 | 0 | 0 | MFN1_chr3_179342709_179399936 | MFN1 | copy fasta | chr3 | 179342709 | 179399936 |
a0001c0001t0009 | 0/0 | 5204 | 11 | 11 | 0 | 0 | 0 | 0 | MFN1_chr3_179342709_179399936 | MFN1 | copy fasta | chr3 | 179342709 | 179399936 |
a0001c0001t0010 | 0/0 | 5213 | 8 | 0 | 0 | 8 | 0 | 0 | MFN1_chr3_179342709_179399936 | MFN1 | copy fasta | chr3 | 179342709 | 179399936 |
a0001c0001t0011 | 0/0 | 5211 | 7 | 0 | 2 | 5 | 0 | 0 | MFN1_chr3_179342709_179399936 | MFN1 | copy fasta | chr3 | 179342709 | 179399936 |
a0001c0001t0012 | 0/0 | 5213 | 6 | 4 | 2 | 0 | 0 | 0 | MFN1_chr3_179342709_179399936 | MFN1 | copy fasta | chr3 | 179342709 | 179399936 |
a0001c0001t0013 | 0/0 | 5212 | 7 | 1 | 6 | 0 | 0 | 0 | MFN1_chr3_179342709_179399936 | MFN1 | copy fasta | chr3 | 179342709 | 179399936 |
a0001c0001t0014 | 0/0 | 5213 | 7 | 0 | 3 | 0 | 2 | 2 | MFN1_chr3_179342709_179399936 | MFN1 | copy fasta | chr3 | 179342709 | 179399936 |
a0001c0001t0015 | 0/0 | 5213 | 6 | 4 | 2 | 0 | 0 | 0 | MFN1_chr3_179342709_179399936 | MFN1 | copy fasta | chr3 | 179342709 | 179399936 |
a0001c0001t0016 | 0/0 | 5212 | 2 | 0 | 2 | 0 | 0 | 0 | MFN1_chr3_179342709_179399936 | MFN1 | copy fasta | chr3 | 179342709 | 179399936 |
a0001c0001t0017 | 0/0 | 5214 | 6 | 3 | 0 | 0 | 0 | 3 | MFN1_chr3_179342709_179399936 | MFN1 | copy fasta | chr3 | 179342709 | 179399936 |
a0001c0001t0018 | 0/0 | 5215 | 5 | 3 | 2 | 0 | 0 | 0 | MFN1_chr3_179342709_179399936 | MFN1 | copy fasta | chr3 | 179342709 | 179399936 |
a0001c0001t0019 | 0/0 | 5212 | 3 | 3 | 0 | 0 | 0 | 0 | MFN1_chr3_179342709_179399936 | MFN1 | copy fasta | chr3 | 179342709 | 179399936 |
a0001c0001t0020 | 0/0 | 5212 | 3 | 2 | 1 | 0 | 0 | 0 | MFN1_chr3_179342709_179399936 | MFN1 | copy fasta | chr3 | 179342709 | 179399936 |
a0001c0001t0021 | 0/0 | 5213 | 3 | 3 | 0 | 0 | 0 | 0 | MFN1_chr3_179342709_179399936 | MFN1 | copy fasta | chr3 | 179342709 | 179399936 |
a0001c0001t0022 | 0/0 | 5214 | 3 | 0 | 1 | 0 | 0 | 2 | MFN1_chr3_179342709_179399936 | MFN1 | copy fasta | chr3 | 179342709 | 179399936 |
a0001c0001t0023 | 0/0 | 5213 | 2 | 2 | 0 | 0 | 0 | 0 | MFN1_chr3_179342709_179399936 | MFN1 | copy fasta | chr3 | 179342709 | 179399936 |
a0001c0001t0024 | 0/0 | 5212 | 2 | 0 | 0 | 2 | 0 | 0 | MFN1_chr3_179342709_179399936 | MFN1 | copy fasta | chr3 | 179342709 | 179399936 |
a0001c0001t0025 | 0/0 | 5209 | 2 | 0 | 2 | 0 | 0 | 0 | MFN1_chr3_179342709_179399936 | MFN1 | copy fasta | chr3 | 179342709 | 179399936 |
a0001c0001t0026 | 0/0 | 5211 | 2 | 2 | 0 | 0 | 0 | 0 | MFN1_chr3_179342709_179399936 | MFN1 | copy fasta | chr3 | 179342709 | 179399936 |
a0001c0001t0028 | 0/0 | 5212 | 2 | 0 | 0 | 1 | 1 | 0 | MFN1_chr3_179342709_179399936 | MFN1 | copy fasta | chr3 | 179342709 | 179399936 |
a0001c0001t0029 | 0/0 | 5212 | 2 | 0 | 0 | 2 | 0 | 0 | MFN1_chr3_179342709_179399936 | MFN1 | copy fasta | chr3 | 179342709 | 179399936 |
a0001c0001t0030 | 0/0 | 5211 | 2 | 0 | 2 | 0 | 0 | 0 | MFN1_chr3_179342709_179399936 | MFN1 | copy fasta | chr3 | 179342709 | 179399936 |
a0001c0001t0031 | 0/0 | 5214 | 2 | 0 | 1 | 1 | 0 | 0 | MFN1_chr3_179342709_179399936 | MFN1 | copy fasta | chr3 | 179342709 | 179399936 |
a0001c0001t0032 | 0/0 | 5215 | 1 | 0 | 1 | 0 | 0 | 0 | MFN1_chr3_179342709_179399936 | MFN1 | copy fasta | chr3 | 179342709 | 179399936 |
a0001c0001t0033 | 0/0 | 5212 | 2 | 2 | 0 | 0 | 0 | 0 | MFN1_chr3_179342709_179399936 | MFN1 | copy fasta | chr3 | 179342709 | 179399936 |
a0001c0001t0034 | 0/0 | 5212 | 2 | 2 | 0 | 0 | 0 | 0 | MFN1_chr3_179342709_179399936 | MFN1 | copy fasta | chr3 | 179342709 | 179399936 |
a0001c0001t0035 | 0/0 | 5213 | 1 | 1 | 0 | 0 | 0 | 0 | MFN1_chr3_179342709_179399936 | MFN1 | copy fasta | chr3 | 179342709 | 179399936 |
a0001c0001t0036 | 0/0 | 5214 | 1 | 1 | 0 | 0 | 0 | 0 | MFN1_chr3_179342709_179399936 | MFN1 | copy fasta | chr3 | 179342709 | 179399936 |
a0001c0001t0037 | 0/0 | 5210 | 1 | 0 | 1 | 0 | 0 | 0 | MFN1_chr3_179342709_179399936 | MFN1 | copy fasta | chr3 | 179342709 | 179399936 |
a0001c0001t0038 | 0/0 | 5212 | 1 | 0 | 0 | 0 | 0 | 1 | MFN1_chr3_179342709_179399936 | MFN1 | copy fasta | chr3 | 179342709 | 179399936 |
a0001c0001t0040 | 0/0 | 5214 | 1 | 1 | 0 | 0 | 0 | 0 | MFN1_chr3_179342709_179399936 | MFN1 | copy fasta | chr3 | 179342709 | 179399936 |
a0001c0001t0041 | 0/0 | 5211 | 1 | 1 | 0 | 0 | 0 | 0 | MFN1_chr3_179342709_179399936 | MFN1 | copy fasta | chr3 | 179342709 | 179399936 |
a0001c0001t0042 | 0/0 | 5212 | 1 | 1 | 0 | 0 | 0 | 0 | MFN1_chr3_179342709_179399936 | MFN1 | copy fasta | chr3 | 179342709 | 179399936 |
a0001c0001t0043 | 0/0 | 5213 | 1 | 0 | 0 | 0 | 0 | 1 | MFN1_chr3_179342709_179399936 | MFN1 | copy fasta | chr3 | 179342709 | 179399936 |
a0001c0001t0044 | 0/0 | 5211 | 1 | 0 | 0 | 1 | 0 | 0 | MFN1_chr3_179342709_179399936 | MFN1 | copy fasta | chr3 | 179342709 | 179399936 |
a0001c0001t0045 | 0/0 | 5204 | 1 | 1 | 0 | 0 | 0 | 0 | MFN1_chr3_179342709_179399936 | MFN1 | copy fasta | chr3 | 179342709 | 179399936 |
a0001c0001t0046 | 0/0 | 5213 | 1 | 0 | 0 | 1 | 0 | 0 | MFN1_chr3_179342709_179399936 | MFN1 | copy fasta | chr3 | 179342709 | 179399936 |
a0001c0001t0047 | 0/0 | 5212 | 1 | 0 | 0 | 1 | 0 | 0 | MFN1_chr3_179342709_179399936 | MFN1 | copy fasta | chr3 | 179342709 | 179399936 |
a0001c0001t0048 | 0/0 | 5213 | 1 | 0 | 0 | 1 | 0 | 0 | MFN1_chr3_179342709_179399936 | MFN1 | copy fasta | chr3 | 179342709 | 179399936 |
a0001c0001t0049 | 0/0 | 5202 | 1 | 1 | 0 | 0 | 0 | 0 | MFN1_chr3_179342709_179399936 | MFN1 | copy fasta | chr3 | 179342709 | 179399936 |
a0001c0001t0050 | 0/0 | 5212 | 1 | 0 | 0 | 1 | 0 | 0 | MFN1_chr3_179342709_179399936 | MFN1 | copy fasta | chr3 | 179342709 | 179399936 |
a0001c0001t0051 | 0/0 | 5212 | 1 | 1 | 0 | 0 | 0 | 0 | MFN1_chr3_179342709_179399936 | MFN1 | copy fasta | chr3 | 179342709 | 179399936 |
a0001c0001t0052 | 0/0 | 5213 | 1 | 1 | 0 | 0 | 0 | 0 | MFN1_chr3_179342709_179399936 | MFN1 | copy fasta | chr3 | 179342709 | 179399936 |
a0001c0002t0004 | 0/0 | 5213 | 2 | 0 | 0 | 1 | 0 | 1 | MFN1_chr3_179342709_179399936 | MFN1 | copy fasta | chr3 | 179342709 | 179399936 |
a0001c0002t0016 | 0/0 | 5212 | 4 | 0 | 0 | 0 | 0 | 4 | MFN1_chr3_179342709_179399936 | MFN1 | copy fasta | chr3 | 179342709 | 179399936 |
a0001c0004t0002 | 0/0 | 5211 | 2 | 0 | 0 | 2 | 0 | 0 | MFN1_chr3_179342709_179399936 | MFN1 | copy fasta | chr3 | 179342709 | 179399936 |
a0001c0005t0027 | 0/0 | 5212 | 2 | 2 | 0 | 0 | 0 | 0 | MFN1_chr3_179342709_179399936 | MFN1 | copy fasta | chr3 | 179342709 | 179399936 |
a0001c0008t0019 | 0/0 | 5212 | 1 | 1 | 0 | 0 | 0 | 0 | MFN1_chr3_179342709_179399936 | MFN1 | copy fasta | chr3 | 179342709 | 179399936 |
a0001c0009t0039 | 0/0 | 5213 | 1 | 1 | 0 | 0 | 0 | 0 | MFN1_chr3_179342709_179399936 | MFN1 | copy fasta | chr3 | 179342709 | 179399936 |
a0002c0003t0001 | 0/0 | 5212 | 1 | 0 | 0 | 1 | 0 | 0 | MFN1_chr3_179342709_179399936 | MFN1 | copy fasta | chr3 | 179342709 | 179399936 |
a0002c0003t0003 | 0/0 | 5213 | 1 | 0 | 0 | 1 | 0 | 0 | MFN1_chr3_179342709_179399936 | MFN1 | copy fasta | chr3 | 179342709 | 179399936 |
a0003c0006t0003 | 0/0 | 5213 | 1 | 0 | 1 | 0 | 0 | 0 | MFN1_chr3_179342709_179399936 | MFN1 | copy fasta | chr3 | 179342709 | 179399936 |
a0004c0007t0012 | 0/0 | 5213 | 1 | 1 | 0 | 0 | 0 | 0 | MFN1_chr3_179342709_179399936 | MFN1 | copy fasta | chr3 | 179342709 | 179399936 |
a0005c0010t0032 | 0/0 | 5215 | 1 | 1 | 0 | 0 | 0 | 0 | MFN1_chr3_179342709_179399936 | MFN1 | copy fasta | chr3 | 179342709 | 179399936 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0002 | 0/0 | 5 | 0 | 0 | 1 | 0 | 4 | MFN1_chr3_179342709_179399936 | MFN1 | chr3 | 179342709 | 179399936 |
a0001c0001t0001g0004 | 0/0 | 3 | 2 | 1 | 0 | 0 | 0 | MFN1_chr3_179342709_179399936 | MFN1 | chr3 | 179342709 | 179399936 |
a0001c0001t0001g0007 | 0/0 | 5 | 0 | 4 | 0 | 0 | 1 | MFN1_chr3_179342709_179399936 | MFN1 | chr3 | 179342709 | 179399936 |
a0001c0001t0001g0008 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | MFN1_chr3_179342709_179399936 | MFN1 | chr3 | 179342709 | 179399936 |
a0001c0001t0001g0010 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | MFN1_chr3_179342709_179399936 | MFN1 | chr3 | 179342709 | 179399936 |
a0001c0001t0001g0011 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | MFN1_chr3_179342709_179399936 | MFN1 | chr3 | 179342709 | 179399936 |
a0001c0001t0001g0012 | 0/1 | 4 | 0 | 2 | 0 | 0 | 1 | MFN1_chr3_179342709_179399936 | MFN1 | chr3 | 179342709 | 179399936 |
a0001c0001t0001g0015 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MFN1_chr3_179342709_179399936 | MFN1 | chr3 | 179342709 | 179399936 |
a0001c0001t0001g0016 | 0/0 | 3 | 0 | 1 | 0 | 0 | 2 | MFN1_chr3_179342709_179399936 | MFN1 | chr3 | 179342709 | 179399936 |
a0001c0001t0001g0018 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | MFN1_chr3_179342709_179399936 | MFN1 | chr3 | 179342709 | 179399936 |
a0001c0001t0001g0019 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MFN1_chr3_179342709_179399936 | MFN1 | chr3 | 179342709 | 179399936 |
a0001c0001t0001g0028 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MFN1_chr3_179342709_179399936 | MFN1 | chr3 | 179342709 | 179399936 |
a0001c0001t0001g0030 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MFN1_chr3_179342709_179399936 | MFN1 | chr3 | 179342709 | 179399936 |
a0001c0001t0001g0031 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MFN1_chr3_179342709_179399936 | MFN1 | chr3 | 179342709 | 179399936 |
a0001c0001t0001g0033 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | MFN1_chr3_179342709_179399936 | MFN1 | chr3 | 179342709 | 179399936 |
a0001c0001t0001g0034 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MFN1_chr3_179342709_179399936 | MFN1 | chr3 | 179342709 | 179399936 |
a0001c0001t0001g0040 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MFN1_chr3_179342709_179399936 | MFN1 | chr3 | 179342709 | 179399936 |
a0001c0001t0001g0041 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MFN1_chr3_179342709_179399936 | MFN1 | chr3 | 179342709 | 179399936 |
a0001c0001t0001g0042 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MFN1_chr3_179342709_179399936 | MFN1 | chr3 | 179342709 | 179399936 |
a0001c0001t0001g0043 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | MFN1_chr3_179342709_179399936 | MFN1 | chr3 | 179342709 | 179399936 |
a0001c0001t0001g0044 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MFN1_chr3_179342709_179399936 | MFN1 | chr3 | 179342709 | 179399936 |
a0001c0001t0001g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFN1_chr3_179342709_179399936 | MFN1 | chr3 | 179342709 | 179399936 |
a0001c0001t0001g0046 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | MFN1_chr3_179342709_179399936 | MFN1 | chr3 | 179342709 | 179399936 |
a0001c0001t0001g0049 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MFN1_chr3_179342709_179399936 | MFN1 | chr3 | 179342709 | 179399936 |
a0001c0001t0001g0067 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MFN1_chr3_179342709_179399936 | MFN1 | chr3 | 179342709 | 179399936 |
a0001c0001t0001g0068 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MFN1_chr3_179342709_179399936 | MFN1 | chr3 | 179342709 | 179399936 |
a0001c0001t0001g0077 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MFN1_chr3_179342709_179399936 | MFN1 | chr3 | 179342709 | 179399936 |
a0001c0001t0001g0078 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MFN1_chr3_179342709_179399936 | MFN1 | chr3 | 179342709 | 179399936 |
a0001c0001t0001g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFN1_chr3_179342709_179399936 | MFN1 | chr3 | 179342709 | 179399936 |
a0001c0001t0001g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFN1_chr3_179342709_179399936 | MFN1 | chr3 | 179342709 | 179399936 |
a0001c0001t0001g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFN1_chr3_179342709_179399936 | MFN1 | chr3 | 179342709 | 179399936 |
a0001c0001t0001g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFN1_chr3_179342709_179399936 | MFN1 | chr3 | 179342709 | 179399936 |
a0001c0001t0001g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFN1_chr3_179342709_179399936 | MFN1 | chr3 | 179342709 | 179399936 |
a0001c0001t0001g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFN1_chr3_179342709_179399936 | MFN1 | chr3 | 179342709 | 179399936 |
a0001c0001t0001g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFN1_chr3_179342709_179399936 | MFN1 | chr3 | 179342709 | 179399936 |
a0001c0001t0001g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFN1_chr3_179342709_179399936 | MFN1 | chr3 | 179342709 | 179399936 |
a0001c0001t0001g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFN1_chr3_179342709_179399936 | MFN1 | chr3 | 179342709 | 179399936 |
a0001c0001t0001g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFN1_chr3_179342709_179399936 | MFN1 | chr3 | 179342709 | 179399936 |
a0001c0001t0001g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFN1_chr3_179342709_179399936 | MFN1 | chr3 | 179342709 | 179399936 |
a0001c0001t0001g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFN1_chr3_179342709_179399936 | MFN1 | chr3 | 179342709 | 179399936 |
a0001c0001t0001g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFN1_chr3_179342709_179399936 | MFN1 | chr3 | 179342709 | 179399936 |
a0001c0001t0001g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFN1_chr3_179342709_179399936 | MFN1 | chr3 | 179342709 | 179399936 |
a0001c0001t0001g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFN1_chr3_179342709_179399936 | MFN1 | chr3 | 179342709 | 179399936 |
a0001c0001t0001g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFN1_chr3_179342709_179399936 | MFN1 | chr3 | 179342709 | 179399936 |
a0001c0001t0001g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFN1_chr3_179342709_179399936 | MFN1 | chr3 | 179342709 | 179399936 |
a0001c0001t0001g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFN1_chr3_179342709_179399936 | MFN1 | chr3 | 179342709 | 179399936 |
a0001c0001t0001g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFN1_chr3_179342709_179399936 | MFN1 | chr3 | 179342709 | 179399936 |
a0001c0001t0001g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFN1_chr3_179342709_179399936 | MFN1 | chr3 | 179342709 | 179399936 |
a0001c0001t0001g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFN1_chr3_179342709_179399936 | MFN1 | chr3 | 179342709 | 179399936 |
a0001c0001t0001g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFN1_chr3_179342709_179399936 | MFN1 | chr3 | 179342709 | 179399936 |
a0001c0001t0001g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFN1_chr3_179342709_179399936 | MFN1 | chr3 | 179342709 | 179399936 |
a0001c0001t0001g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFN1_chr3_179342709_179399936 | MFN1 | chr3 | 179342709 | 179399936 |
a0001c0001t0001g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFN1_chr3_179342709_179399936 | MFN1 | chr3 | 179342709 | 179399936 |
a0001c0001t0001g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFN1_chr3_179342709_179399936 | MFN1 | chr3 | 179342709 | 179399936 |
a0001c0001t0001g0143 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MFN1_chr3_179342709_179399936 | MFN1 | chr3 | 179342709 | 179399936 |
a0001c0001t0001g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFN1_chr3_179342709_179399936 | MFN1 | chr3 | 179342709 | 179399936 |
a0001c0001t0001g0145 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MFN1_chr3_179342709_179399936 | MFN1 | chr3 | 179342709 | 179399936 |
a0001c0001t0001g0146 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MFN1_chr3_179342709_179399936 | MFN1 | chr3 | 179342709 | 179399936 |
a0001c0001t0001g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFN1_chr3_179342709_179399936 | MFN1 | chr3 | 179342709 | 179399936 |
a0001c0001t0001g0151 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MFN1_chr3_179342709_179399936 | MFN1 | chr3 | 179342709 | 179399936 |
a0001c0001t0001g0152 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MFN1_chr3_179342709_179399936 | MFN1 | chr3 | 179342709 | 179399936 |
a0001c0001t0001g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFN1_chr3_179342709_179399936 | MFN1 | chr3 | 179342709 | 179399936 |
a0001c0001t0001g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFN1_chr3_179342709_179399936 | MFN1 | chr3 | 179342709 | 179399936 |
a0001c0001t0001g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFN1_chr3_179342709_179399936 | MFN1 | chr3 | 179342709 | 179399936 |
a0001c0001t0001g0217 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MFN1_chr3_179342709_179399936 | MFN1 | chr3 | 179342709 | 179399936 |
a0001c0001t0001g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFN1_chr3_179342709_179399936 | MFN1 | chr3 | 179342709 | 179399936 |
a0001c0001t0001g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFN1_chr3_179342709_179399936 | MFN1 | chr3 | 179342709 | 179399936 |
a0001c0001t0001g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFN1_chr3_179342709_179399936 | MFN1 | chr3 | 179342709 | 179399936 |
a0001c0001t0001g0232 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MFN1_chr3_179342709_179399936 | MFN1 | chr3 | 179342709 | 179399936 |
a0001c0001t0001g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFN1_chr3_179342709_179399936 | MFN1 | chr3 | 179342709 | 179399936 |
a0001c0001t0001g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFN1_chr3_179342709_179399936 | MFN1 | chr3 | 179342709 | 179399936 |
a0001c0001t0001g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFN1_chr3_179342709_179399936 | MFN1 | chr3 | 179342709 | 179399936 |
a0001c0001t0001g0239 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MFN1_chr3_179342709_179399936 | MFN1 | chr3 | 179342709 | 179399936 |
a0001c0001t0001g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFN1_chr3_179342709_179399936 | MFN1 | chr3 | 179342709 | 179399936 |
a0001c0001t0001g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFN1_chr3_179342709_179399936 | MFN1 | chr3 | 179342709 | 179399936 |
a0001c0001t0001g0243 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MFN1_chr3_179342709_179399936 | MFN1 | chr3 | 179342709 | 179399936 |
a0001c0001t0001g0244 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MFN1_chr3_179342709_179399936 | MFN1 | chr3 | 179342709 | 179399936 |
a0001c0001t0001g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFN1_chr3_179342709_179399936 | MFN1 | chr3 | 179342709 | 179399936 |
a0001c0001t0001g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFN1_chr3_179342709_179399936 | MFN1 | chr3 | 179342709 | 179399936 |
a0001c0001t0001g0249 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFN1_chr3_179342709_179399936 | MFN1 | chr3 | 179342709 | 179399936 |
a0001c0001t0001g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFN1_chr3_179342709_179399936 | MFN1 | chr3 | 179342709 | 179399936 |
a0001c0001t0001g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFN1_chr3_179342709_179399936 | MFN1 | chr3 | 179342709 | 179399936 |
a0001c0001t0001g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFN1_chr3_179342709_179399936 | MFN1 | chr3 | 179342709 | 179399936 |
a0001c0001t0001g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFN1_chr3_179342709_179399936 | MFN1 | chr3 | 179342709 | 179399936 |
a0001c0001t0001g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFN1_chr3_179342709_179399936 | MFN1 | chr3 | 179342709 | 179399936 |
a0001c0001t0001g0264 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MFN1_chr3_179342709_179399936 | MFN1 | chr3 | 179342709 | 179399936 |
a0001c0001t0001g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFN1_chr3_179342709_179399936 | MFN1 | chr3 | 179342709 | 179399936 |
a0001c0001t0001g0267 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MFN1_chr3_179342709_179399936 | MFN1 | chr3 | 179342709 | 179399936 |
a0001c0001t0001g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFN1_chr3_179342709_179399936 | MFN1 | chr3 | 179342709 | 179399936 |
a0001c0001t0001g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFN1_chr3_179342709_179399936 | MFN1 | chr3 | 179342709 | 179399936 |
a0001c0001t0001g0273 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFN1_chr3_179342709_179399936 | MFN1 | chr3 | 179342709 | 179399936 |
a0001c0001t0001g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFN1_chr3_179342709_179399936 | MFN1 | chr3 | 179342709 | 179399936 |
a0001c0001t0001g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFN1_chr3_179342709_179399936 | MFN1 | chr3 | 179342709 | 179399936 |
a0001c0001t0001g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFN1_chr3_179342709_179399936 | MFN1 | chr3 | 179342709 | 179399936 |
a0001c0001t0001g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFN1_chr3_179342709_179399936 | MFN1 | chr3 | 179342709 | 179399936 |
a0001c0001t0001g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFN1_chr3_179342709_179399936 | MFN1 | chr3 | 179342709 | 179399936 |
a0001c0001t0001g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFN1_chr3_179342709_179399936 | MFN1 | chr3 | 179342709 | 179399936 |
a0001c0001t0002g0003 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | MFN1_chr3_179342709_179399936 | MFN1 | chr3 | 179342709 | 179399936 |
a0001c0001t0002g0005 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | MFN1_chr3_179342709_179399936 | MFN1 | chr3 | 179342709 | 179399936 |
a0001c0001t0002g0006 | 0/0 | 4 | 0 | 2 | 1 | 0 | 1 | MFN1_chr3_179342709_179399936 | MFN1 | chr3 | 179342709 | 179399936 |
a0001c0001t0002g0017 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MFN1_chr3_179342709_179399936 | MFN1 | chr3 | 179342709 | 179399936 |
a0001c0001t0002g0036 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MFN1_chr3_179342709_179399936 | MFN1 | chr3 | 179342709 | 179399936 |
a0001c0001t0002g0038 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MFN1_chr3_179342709_179399936 | MFN1 | chr3 | 179342709 | 179399936 |
a0001c0001t0002g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFN1_chr3_179342709_179399936 | MFN1 | chr3 | 179342709 | 179399936 |
a0001c0001t0002g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFN1_chr3_179342709_179399936 | MFN1 | chr3 | 179342709 | 179399936 |
a0001c0001t0002g0158 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MFN1_chr3_179342709_179399936 | MFN1 | chr3 | 179342709 | 179399936 |
a0001c0001t0002g0159 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MFN1_chr3_179342709_179399936 | MFN1 | chr3 | 179342709 | 179399936 |
a0001c0001t0002g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFN1_chr3_179342709_179399936 | MFN1 | chr3 | 179342709 | 179399936 |
a0001c0001t0002g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFN1_chr3_179342709_179399936 | MFN1 | chr3 | 179342709 | 179399936 |
a0001c0001t0002g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFN1_chr3_179342709_179399936 | MFN1 | chr3 | 179342709 | 179399936 |
a0001c0001t0002g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFN1_chr3_179342709_179399936 | MFN1 | chr3 | 179342709 | 179399936 |
a0001c0001t0002g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFN1_chr3_179342709_179399936 | MFN1 | chr3 | 179342709 | 179399936 |
a0001c0001t0002g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFN1_chr3_179342709_179399936 | MFN1 | chr3 | 179342709 | 179399936 |
a0001c0001t0002g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFN1_chr3_179342709_179399936 | MFN1 | chr3 | 179342709 | 179399936 |
a0001c0001t0002g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFN1_chr3_179342709_179399936 | MFN1 | chr3 | 179342709 | 179399936 |
a0001c0001t0002g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFN1_chr3_179342709_179399936 | MFN1 | chr3 | 179342709 | 179399936 |
a0001c0001t0002g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFN1_chr3_179342709_179399936 | MFN1 | chr3 | 179342709 | 179399936 |
a0001c0001t0002g0178 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MFN1_chr3_179342709_179399936 | MFN1 | chr3 | 179342709 | 179399936 |
a0001c0001t0002g0181 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MFN1_chr3_179342709_179399936 | MFN1 | chr3 | 179342709 | 179399936 |
a0001c0001t0002g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFN1_chr3_179342709_179399936 | MFN1 | chr3 | 179342709 | 179399936 |
a0001c0001t0002g0184 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MFN1_chr3_179342709_179399936 | MFN1 | chr3 | 179342709 | 179399936 |
a0001c0001t0002g0190 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MFN1_chr3_179342709_179399936 | MFN1 | chr3 | 179342709 | 179399936 |
a0001c0001t0002g0191 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MFN1_chr3_179342709_179399936 | MFN1 | chr3 | 179342709 | 179399936 |
a0001c0001t0002g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFN1_chr3_179342709_179399936 | MFN1 | chr3 | 179342709 | 179399936 |
a0001c0001t0002g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFN1_chr3_179342709_179399936 | MFN1 | chr3 | 179342709 | 179399936 |
a0001c0001t0002g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFN1_chr3_179342709_179399936 | MFN1 | chr3 | 179342709 | 179399936 |
a0001c0001t0002g0204 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MFN1_chr3_179342709_179399936 | MFN1 | chr3 | 179342709 | 179399936 |
a0001c0001t0002g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFN1_chr3_179342709_179399936 | MFN1 | chr3 | 179342709 | 179399936 |
a0001c0001t0002g0211 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MFN1_chr3_179342709_179399936 | MFN1 | chr3 | 179342709 | 179399936 |
a0001c0001t0002g0218 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MFN1_chr3_179342709_179399936 | MFN1 | chr3 | 179342709 | 179399936 |
a0001c0001t0002g0219 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MFN1_chr3_179342709_179399936 | MFN1 | chr3 | 179342709 | 179399936 |
a0001c0001t0002g0220 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MFN1_chr3_179342709_179399936 | MFN1 | chr3 | 179342709 | 179399936 |
a0001c0001t0002g0221 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MFN1_chr3_179342709_179399936 | MFN1 | chr3 | 179342709 | 179399936 |
a0001c0001t0002g0222 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MFN1_chr3_179342709_179399936 | MFN1 | chr3 | 179342709 | 179399936 |
a0001c0001t0002g0223 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MFN1_chr3_179342709_179399936 | MFN1 | chr3 | 179342709 | 179399936 |
a0001c0001t0002g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFN1_chr3_179342709_179399936 | MFN1 | chr3 | 179342709 | 179399936 |
a0001c0001t0003g0002 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFN1_chr3_179342709_179399936 | MFN1 | chr3 | 179342709 | 179399936 |
a0001c0001t0003g0011 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFN1_chr3_179342709_179399936 | MFN1 | chr3 | 179342709 | 179399936 |
a0001c0001t0003g0015 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFN1_chr3_179342709_179399936 | MFN1 | chr3 | 179342709 | 179399936 |
a0001c0001t0003g0033 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MFN1_chr3_179342709_179399936 | MFN1 | chr3 | 179342709 | 179399936 |
a0001c0001t0003g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFN1_chr3_179342709_179399936 | MFN1 | chr3 | 179342709 | 179399936 |
a0001c0001t0003g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFN1_chr3_179342709_179399936 | MFN1 | chr3 | 179342709 | 179399936 |
a0001c0001t0003g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFN1_chr3_179342709_179399936 | MFN1 | chr3 | 179342709 | 179399936 |
a0001c0001t0003g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFN1_chr3_179342709_179399936 | MFN1 | chr3 | 179342709 | 179399936 |
a0001c0001t0003g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFN1_chr3_179342709_179399936 | MFN1 | chr3 | 179342709 | 179399936 |
a0001c0001t0003g0133 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MFN1_chr3_179342709_179399936 | MFN1 | chr3 | 179342709 | 179399936 |
a0001c0001t0003g0136 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MFN1_chr3_179342709_179399936 | MFN1 | chr3 | 179342709 | 179399936 |
a0001c0001t0003g0137 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MFN1_chr3_179342709_179399936 | MFN1 | chr3 | 179342709 | 179399936 |
a0001c0001t0003g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFN1_chr3_179342709_179399936 | MFN1 | chr3 | 179342709 | 179399936 |
a0001c0001t0003g0253 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MFN1_chr3_179342709_179399936 | MFN1 | chr3 | 179342709 | 179399936 |
a0001c0001t0003g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFN1_chr3_179342709_179399936 | MFN1 | chr3 | 179342709 | 179399936 |
a0001c0001t0003g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFN1_chr3_179342709_179399936 | MFN1 | chr3 | 179342709 | 179399936 |
a0001c0001t0003g0271 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFN1_chr3_179342709_179399936 | MFN1 | chr3 | 179342709 | 179399936 |
a0001c0001t0003g0272 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFN1_chr3_179342709_179399936 | MFN1 | chr3 | 179342709 | 179399936 |
a0001c0001t0004g0001 | 0/0 | 6 | 0 | 1 | 4 | 1 | 0 | MFN1_chr3_179342709_179399936 | MFN1 | chr3 | 179342709 | 179399936 |
a0001c0001t0004g0026 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MFN1_chr3_179342709_179399936 | MFN1 | chr3 | 179342709 | 179399936 |
a0001c0001t0004g0069 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MFN1_chr3_179342709_179399936 | MFN1 | chr3 | 179342709 | 179399936 |
a0001c0001t0004g0079 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MFN1_chr3_179342709_179399936 | MFN1 | chr3 | 179342709 | 179399936 |
a0001c0001t0004g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFN1_chr3_179342709_179399936 | MFN1 | chr3 | 179342709 | 179399936 |
a0001c0001t0004g0085 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MFN1_chr3_179342709_179399936 | MFN1 | chr3 | 179342709 | 179399936 |
a0001c0001t0004g0086 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MFN1_chr3_179342709_179399936 | MFN1 | chr3 | 179342709 | 179399936 |
a0001c0001t0004g0089 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MFN1_chr3_179342709_179399936 | MFN1 | chr3 | 179342709 | 179399936 |
a0001c0001t0004g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFN1_chr3_179342709_179399936 | MFN1 | chr3 | 179342709 | 179399936 |
a0001c0001t0004g0092 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MFN1_chr3_179342709_179399936 | MFN1 | chr3 | 179342709 | 179399936 |
a0001c0001t0004g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MFN1_chr3_179342709_179399936 | MFN1 | chr3 | 179342709 | 179399936 |
a0001c0001t0005g0003 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MFN1_chr3_179342709_179399936 | MFN1 | chr3 | 179342709 | 179399936 |
a0001c0001t0005g0006 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MFN1_chr3_179342709_179399936 | MFN1 | chr3 | 179342709 | 179399936 |
a0001c0001t0005g0017 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MFN1_chr3_179342709_179399936 | MFN1 | chr3 | 179342709 | 179399936 |
a0001c0001t0005g0038 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MFN1_chr3_179342709_179399936 | MFN1 | chr3 | 179342709 | 179399936 |
a0001c0001t0005g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFN1_chr3_179342709_179399936 | MFN1 | chr3 | 179342709 | 179399936 |
a0001c0001t0005g0148 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MFN1_chr3_179342709_179399936 | MFN1 | chr3 | 179342709 | 179399936 |
a0001c0001t0005g0161 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MFN1_chr3_179342709_179399936 | MFN1 | chr3 | 179342709 | 179399936 |
a0001c0001t0005g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFN1_chr3_179342709_179399936 | MFN1 | chr3 | 179342709 | 179399936 |
a0001c0001t0005g0176 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MFN1_chr3_179342709_179399936 | MFN1 | chr3 | 179342709 | 179399936 |
a0001c0001t0005g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFN1_chr3_179342709_179399936 | MFN1 | chr3 | 179342709 | 179399936 |
a0001c0001t0005g0180 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MFN1_chr3_179342709_179399936 | MFN1 | chr3 | 179342709 | 179399936 |
a0001c0001t0005g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFN1_chr3_179342709_179399936 | MFN1 | chr3 | 179342709 | 179399936 |
a0001c0001t0005g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFN1_chr3_179342709_179399936 | MFN1 | chr3 | 179342709 | 179399936 |
a0001c0001t0005g0203 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MFN1_chr3_179342709_179399936 | MFN1 | chr3 | 179342709 | 179399936 |
a0001c0001t0005g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFN1_chr3_179342709_179399936 | MFN1 | chr3 | 179342709 | 179399936 |
a0001c0001t0006g0009 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MFN1_chr3_179342709_179399936 | MFN1 | chr3 | 179342709 | 179399936 |
a0001c0001t0006g0020 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MFN1_chr3_179342709_179399936 | MFN1 | chr3 | 179342709 | 179399936 |
a0001c0001t0006g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFN1_chr3_179342709_179399936 | MFN1 | chr3 | 179342709 | 179399936 |
a0001c0001t0006g0048 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MFN1_chr3_179342709_179399936 | MFN1 | chr3 | 179342709 | 179399936 |
a0001c0001t0006g0290 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFN1_chr3_179342709_179399936 | MFN1 | chr3 | 179342709 | 179399936 |
a0001c0001t0006g0292 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFN1_chr3_179342709_179399936 | MFN1 | chr3 | 179342709 | 179399936 |
a0001c0001t0006g0295 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFN1_chr3_179342709_179399936 | MFN1 | chr3 | 179342709 | 179399936 |
a0001c0001t0006g0296 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFN1_chr3_179342709_179399936 | MFN1 | chr3 | 179342709 | 179399936 |
a0001c0001t0006g0297 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFN1_chr3_179342709_179399936 | MFN1 | chr3 | 179342709 | 179399936 |
a0001c0001t0006g0298 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFN1_chr3_179342709_179399936 | MFN1 | chr3 | 179342709 | 179399936 |
a0001c0001t0007g0019 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MFN1_chr3_179342709_179399936 | MFN1 | chr3 | 179342709 | 179399936 |
a0001c0001t0007g0088 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MFN1_chr3_179342709_179399936 | MFN1 | chr3 | 179342709 | 179399936 |
a0001c0001t0007g0140 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MFN1_chr3_179342709_179399936 | MFN1 | chr3 | 179342709 | 179399936 |
a0001c0001t0007g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFN1_chr3_179342709_179399936 | MFN1 | chr3 | 179342709 | 179399936 |
a0001c0001t0007g0248 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MFN1_chr3_179342709_179399936 | MFN1 | chr3 | 179342709 | 179399936 |
a0001c0001t0007g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFN1_chr3_179342709_179399936 | MFN1 | chr3 | 179342709 | 179399936 |
a0001c0001t0007g0258 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MFN1_chr3_179342709_179399936 | MFN1 | chr3 | 179342709 | 179399936 |
a0001c0001t0007g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFN1_chr3_179342709_179399936 | MFN1 | chr3 | 179342709 | 179399936 |
a0001c0001t0007g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFN1_chr3_179342709_179399936 | MFN1 | chr3 | 179342709 | 179399936 |
a0001c0001t0007g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFN1_chr3_179342709_179399936 | MFN1 | chr3 | 179342709 | 179399936 |
a0001c0001t0007g0265 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MFN1_chr3_179342709_179399936 | MFN1 | chr3 | 179342709 | 179399936 |
a0001c0001t0007g0274 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MFN1_chr3_179342709_179399936 | MFN1 | chr3 | 179342709 | 179399936 |
a0001c0001t0008g0017 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFN1_chr3_179342709_179399936 | MFN1 | chr3 | 179342709 | 179399936 |
a0001c0001t0008g0037 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MFN1_chr3_179342709_179399936 | MFN1 | chr3 | 179342709 | 179399936 |
a0001c0001t0008g0149 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MFN1_chr3_179342709_179399936 | MFN1 | chr3 | 179342709 | 179399936 |
a0001c0001t0008g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFN1_chr3_179342709_179399936 | MFN1 | chr3 | 179342709 | 179399936 |
a0001c0001t0008g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFN1_chr3_179342709_179399936 | MFN1 | chr3 | 179342709 | 179399936 |
a0001c0001t0008g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFN1_chr3_179342709_179399936 | MFN1 | chr3 | 179342709 | 179399936 |
a0001c0001t0008g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFN1_chr3_179342709_179399936 | MFN1 | chr3 | 179342709 | 179399936 |
a0001c0001t0008g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFN1_chr3_179342709_179399936 | MFN1 | chr3 | 179342709 | 179399936 |
a0001c0001t0008g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFN1_chr3_179342709_179399936 | MFN1 | chr3 | 179342709 | 179399936 |
a0001c0001t0008g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFN1_chr3_179342709_179399936 | MFN1 | chr3 | 179342709 | 179399936 |
a0001c0001t0008g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFN1_chr3_179342709_179399936 | MFN1 | chr3 | 179342709 | 179399936 |
a0001c0001t0009g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFN1_chr3_179342709_179399936 | MFN1 | chr3 | 179342709 | 179399936 |
a0001c0001t0009g0025 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MFN1_chr3_179342709_179399936 | MFN1 | chr3 | 179342709 | 179399936 |
a0001c0001t0009g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFN1_chr3_179342709_179399936 | MFN1 | chr3 | 179342709 | 179399936 |
a0001c0001t0009g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFN1_chr3_179342709_179399936 | MFN1 | chr3 | 179342709 | 179399936 |
a0001c0001t0009g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFN1_chr3_179342709_179399936 | MFN1 | chr3 | 179342709 | 179399936 |
a0001c0001t0009g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFN1_chr3_179342709_179399936 | MFN1 | chr3 | 179342709 | 179399936 |
a0001c0001t0009g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFN1_chr3_179342709_179399936 | MFN1 | chr3 | 179342709 | 179399936 |
a0001c0001t0009g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFN1_chr3_179342709_179399936 | MFN1 | chr3 | 179342709 | 179399936 |
a0001c0001t0009g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFN1_chr3_179342709_179399936 | MFN1 | chr3 | 179342709 | 179399936 |
a0001c0001t0009g0289 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFN1_chr3_179342709_179399936 | MFN1 | chr3 | 179342709 | 179399936 |
a0001c0001t0010g0001 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | MFN1_chr3_179342709_179399936 | MFN1 | chr3 | 179342709 | 179399936 |
a0001c0001t0010g0027 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MFN1_chr3_179342709_179399936 | MFN1 | chr3 | 179342709 | 179399936 |
a0001c0001t0010g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFN1_chr3_179342709_179399936 | MFN1 | chr3 | 179342709 | 179399936 |
a0001c0001t0010g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFN1_chr3_179342709_179399936 | MFN1 | chr3 | 179342709 | 179399936 |
a0001c0001t0011g0035 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | MFN1_chr3_179342709_179399936 | MFN1 | chr3 | 179342709 | 179399936 |
a0001c0001t0011g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFN1_chr3_179342709_179399936 | MFN1 | chr3 | 179342709 | 179399936 |
a0001c0001t0011g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFN1_chr3_179342709_179399936 | MFN1 | chr3 | 179342709 | 179399936 |
a0001c0001t0011g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFN1_chr3_179342709_179399936 | MFN1 | chr3 | 179342709 | 179399936 |
a0001c0001t0011g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFN1_chr3_179342709_179399936 | MFN1 | chr3 | 179342709 | 179399936 |
a0001c0001t0011g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFN1_chr3_179342709_179399936 | MFN1 | chr3 | 179342709 | 179399936 |
a0001c0001t0012g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFN1_chr3_179342709_179399936 | MFN1 | chr3 | 179342709 | 179399936 |
a0001c0001t0012g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFN1_chr3_179342709_179399936 | MFN1 | chr3 | 179342709 | 179399936 |
a0001c0001t0012g0059 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MFN1_chr3_179342709_179399936 | MFN1 | chr3 | 179342709 | 179399936 |
a0001c0001t0012g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFN1_chr3_179342709_179399936 | MFN1 | chr3 | 179342709 | 179399936 |
a0001c0001t0012g0061 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MFN1_chr3_179342709_179399936 | MFN1 | chr3 | 179342709 | 179399936 |
a0001c0001t0012g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFN1_chr3_179342709_179399936 | MFN1 | chr3 | 179342709 | 179399936 |
a0001c0001t0013g0013 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | MFN1_chr3_179342709_179399936 | MFN1 | chr3 | 179342709 | 179399936 |
a0001c0001t0013g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFN1_chr3_179342709_179399936 | MFN1 | chr3 | 179342709 | 179399936 |
a0001c0001t0013g0212 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MFN1_chr3_179342709_179399936 | MFN1 | chr3 | 179342709 | 179399936 |
a0001c0001t0013g0213 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MFN1_chr3_179342709_179399936 | MFN1 | chr3 | 179342709 | 179399936 |
a0001c0001t0013g0214 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MFN1_chr3_179342709_179399936 | MFN1 | chr3 | 179342709 | 179399936 |
a0001c0001t0014g0014 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | MFN1_chr3_179342709_179399936 | MFN1 | chr3 | 179342709 | 179399936 |
a0001c0001t0014g0070 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MFN1_chr3_179342709_179399936 | MFN1 | chr3 | 179342709 | 179399936 |
a0001c0001t0014g0071 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MFN1_chr3_179342709_179399936 | MFN1 | chr3 | 179342709 | 179399936 |
a0001c0001t0014g0072 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MFN1_chr3_179342709_179399936 | MFN1 | chr3 | 179342709 | 179399936 |
a0001c0001t0014g0074 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MFN1_chr3_179342709_179399936 | MFN1 | chr3 | 179342709 | 179399936 |
a0001c0001t0014g0076 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MFN1_chr3_179342709_179399936 | MFN1 | chr3 | 179342709 | 179399936 |
a0001c0001t0015g0021 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MFN1_chr3_179342709_179399936 | MFN1 | chr3 | 179342709 | 179399936 |
a0001c0001t0015g0299 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MFN1_chr3_179342709_179399936 | MFN1 | chr3 | 179342709 | 179399936 |
a0001c0001t0015g0300 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MFN1_chr3_179342709_179399936 | MFN1 | chr3 | 179342709 | 179399936 |
a0001c0001t0015g0301 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFN1_chr3_179342709_179399936 | MFN1 | chr3 | 179342709 | 179399936 |
a0001c0001t0015g0302 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFN1_chr3_179342709_179399936 | MFN1 | chr3 | 179342709 | 179399936 |
a0001c0001t0016g0080 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MFN1_chr3_179342709_179399936 | MFN1 | chr3 | 179342709 | 179399936 |
a0001c0001t0016g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MFN1_chr3_179342709_179399936 | MFN1 | chr3 | 179342709 | 179399936 |
a0001c0001t0017g0039 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MFN1_chr3_179342709_179399936 | MFN1 | chr3 | 179342709 | 179399936 |
a0001c0001t0017g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFN1_chr3_179342709_179399936 | MFN1 | chr3 | 179342709 | 179399936 |
a0001c0001t0017g0093 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MFN1_chr3_179342709_179399936 | MFN1 | chr3 | 179342709 | 179399936 |
a0001c0001t0017g0094 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MFN1_chr3_179342709_179399936 | MFN1 | chr3 | 179342709 | 179399936 |
a0001c0001t0017g0095 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MFN1_chr3_179342709_179399936 | MFN1 | chr3 | 179342709 | 179399936 |
a0001c0001t0018g0022 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | MFN1_chr3_179342709_179399936 | MFN1 | chr3 | 179342709 | 179399936 |
a0001c0001t0018g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFN1_chr3_179342709_179399936 | MFN1 | chr3 | 179342709 | 179399936 |
a0001c0001t0018g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFN1_chr3_179342709_179399936 | MFN1 | chr3 | 179342709 | 179399936 |
a0001c0001t0018g0053 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MFN1_chr3_179342709_179399936 | MFN1 | chr3 | 179342709 | 179399936 |
a0001c0001t0019g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFN1_chr3_179342709_179399936 | MFN1 | chr3 | 179342709 | 179399936 |
a0001c0001t0019g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFN1_chr3_179342709_179399936 | MFN1 | chr3 | 179342709 | 179399936 |
a0001c0001t0019g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFN1_chr3_179342709_179399936 | MFN1 | chr3 | 179342709 | 179399936 |
a0001c0001t0020g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MFN1_chr3_179342709_179399936 | MFN1 | chr3 | 179342709 | 179399936 |
a0001c0001t0020g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFN1_chr3_179342709_179399936 | MFN1 | chr3 | 179342709 | 179399936 |
a0001c0001t0020g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFN1_chr3_179342709_179399936 | MFN1 | chr3 | 179342709 | 179399936 |
a0001c0001t0021g0009 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | MFN1_chr3_179342709_179399936 | MFN1 | chr3 | 179342709 | 179399936 |
a0001c0001t0022g0014 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MFN1_chr3_179342709_179399936 | MFN1 | chr3 | 179342709 | 179399936 |
a0001c0001t0022g0073 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MFN1_chr3_179342709_179399936 | MFN1 | chr3 | 179342709 | 179399936 |
a0001c0001t0022g0075 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MFN1_chr3_179342709_179399936 | MFN1 | chr3 | 179342709 | 179399936 |
a0001c0001t0023g0303 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFN1_chr3_179342709_179399936 | MFN1 | chr3 | 179342709 | 179399936 |
a0001c0001t0023g0304 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFN1_chr3_179342709_179399936 | MFN1 | chr3 | 179342709 | 179399936 |
a0001c0001t0024g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFN1_chr3_179342709_179399936 | MFN1 | chr3 | 179342709 | 179399936 |
a0001c0001t0024g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFN1_chr3_179342709_179399936 | MFN1 | chr3 | 179342709 | 179399936 |
a0001c0001t0025g0020 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MFN1_chr3_179342709_179399936 | MFN1 | chr3 | 179342709 | 179399936 |
a0001c0001t0025g0291 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MFN1_chr3_179342709_179399936 | MFN1 | chr3 | 179342709 | 179399936 |
a0001c0001t0026g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFN1_chr3_179342709_179399936 | MFN1 | chr3 | 179342709 | 179399936 |
a0001c0001t0026g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFN1_chr3_179342709_179399936 | MFN1 | chr3 | 179342709 | 179399936 |
a0001c0001t0028g0185 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MFN1_chr3_179342709_179399936 | MFN1 | chr3 | 179342709 | 179399936 |
a0001c0001t0028g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFN1_chr3_179342709_179399936 | MFN1 | chr3 | 179342709 | 179399936 |
a0001c0001t0029g0010 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFN1_chr3_179342709_179399936 | MFN1 | chr3 | 179342709 | 179399936 |
a0001c0001t0029g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFN1_chr3_179342709_179399936 | MFN1 | chr3 | 179342709 | 179399936 |
a0001c0001t0030g0013 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MFN1_chr3_179342709_179399936 | MFN1 | chr3 | 179342709 | 179399936 |
a0001c0001t0030g0224 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MFN1_chr3_179342709_179399936 | MFN1 | chr3 | 179342709 | 179399936 |
a0001c0001t0031g0132 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MFN1_chr3_179342709_179399936 | MFN1 | chr3 | 179342709 | 179399936 |
a0001c0001t0031g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFN1_chr3_179342709_179399936 | MFN1 | chr3 | 179342709 | 179399936 |
a0001c0001t0032g0229 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MFN1_chr3_179342709_179399936 | MFN1 | chr3 | 179342709 | 179399936 |
a0001c0001t0033g0004 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MFN1_chr3_179342709_179399936 | MFN1 | chr3 | 179342709 | 179399936 |
a0001c0001t0034g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFN1_chr3_179342709_179399936 | MFN1 | chr3 | 179342709 | 179399936 |
a0001c0001t0034g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFN1_chr3_179342709_179399936 | MFN1 | chr3 | 179342709 | 179399936 |
a0001c0001t0035g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFN1_chr3_179342709_179399936 | MFN1 | chr3 | 179342709 | 179399936 |
a0001c0001t0036g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFN1_chr3_179342709_179399936 | MFN1 | chr3 | 179342709 | 179399936 |
a0001c0001t0037g0293 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MFN1_chr3_179342709_179399936 | MFN1 | chr3 | 179342709 | 179399936 |
a0001c0001t0038g0294 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MFN1_chr3_179342709_179399936 | MFN1 | chr3 | 179342709 | 179399936 |
a0001c0001t0040g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFN1_chr3_179342709_179399936 | MFN1 | chr3 | 179342709 | 179399936 |
a0001c0001t0041g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFN1_chr3_179342709_179399936 | MFN1 | chr3 | 179342709 | 179399936 |
a0001c0001t0042g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFN1_chr3_179342709_179399936 | MFN1 | chr3 | 179342709 | 179399936 |
a0001c0001t0043g0206 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MFN1_chr3_179342709_179399936 | MFN1 | chr3 | 179342709 | 179399936 |
a0001c0001t0044g0003 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFN1_chr3_179342709_179399936 | MFN1 | chr3 | 179342709 | 179399936 |
a0001c0001t0045g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFN1_chr3_179342709_179399936 | MFN1 | chr3 | 179342709 | 179399936 |
a0001c0001t0046g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFN1_chr3_179342709_179399936 | MFN1 | chr3 | 179342709 | 179399936 |
a0001c0001t0047g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFN1_chr3_179342709_179399936 | MFN1 | chr3 | 179342709 | 179399936 |
a0001c0001t0048g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFN1_chr3_179342709_179399936 | MFN1 | chr3 | 179342709 | 179399936 |
a0001c0001t0049g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFN1_chr3_179342709_179399936 | MFN1 | chr3 | 179342709 | 179399936 |
a0001c0001t0050g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFN1_chr3_179342709_179399936 | MFN1 | chr3 | 179342709 | 179399936 |
a0001c0001t0051g0252 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFN1_chr3_179342709_179399936 | MFN1 | chr3 | 179342709 | 179399936 |
a0001c0001t0052g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFN1_chr3_179342709_179399936 | MFN1 | chr3 | 179342709 | 179399936 |
a0001c0002t0004g0282 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MFN1_chr3_179342709_179399936 | MFN1 | chr3 | 179342709 | 179399936 |
a0001c0002t0004g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFN1_chr3_179342709_179399936 | MFN1 | chr3 | 179342709 | 179399936 |
a0001c0002t0016g0281 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MFN1_chr3_179342709_179399936 | MFN1 | chr3 | 179342709 | 179399936 |
a0001c0002t0016g0283 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MFN1_chr3_179342709_179399936 | MFN1 | chr3 | 179342709 | 179399936 |
a0001c0002t0016g0284 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MFN1_chr3_179342709_179399936 | MFN1 | chr3 | 179342709 | 179399936 |
a0001c0002t0016g0286 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MFN1_chr3_179342709_179399936 | MFN1 | chr3 | 179342709 | 179399936 |
a0001c0004t0002g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFN1_chr3_179342709_179399936 | MFN1 | chr3 | 179342709 | 179399936 |
a0001c0004t0002g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFN1_chr3_179342709_179399936 | MFN1 | chr3 | 179342709 | 179399936 |
a0001c0005t0027g0287 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFN1_chr3_179342709_179399936 | MFN1 | chr3 | 179342709 | 179399936 |
a0001c0005t0027g0288 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFN1_chr3_179342709_179399936 | MFN1 | chr3 | 179342709 | 179399936 |
a0001c0008t0019g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFN1_chr3_179342709_179399936 | MFN1 | chr3 | 179342709 | 179399936 |
a0001c0009t0039g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFN1_chr3_179342709_179399936 | MFN1 | chr3 | 179342709 | 179399936 |
a0002c0003t0001g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFN1_chr3_179342709_179399936 | MFN1 | chr3 | 179342709 | 179399936 |
a0002c0003t0003g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFN1_chr3_179342709_179399936 | MFN1 | chr3 | 179342709 | 179399936 |
a0003c0006t0003g0245 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MFN1_chr3_179342709_179399936 | MFN1 | chr3 | 179342709 | 179399936 |
a0004c0007t0012g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFN1_chr3_179342709_179399936 | MFN1 | chr3 | 179342709 | 179399936 |
a0005c0010t0032g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFN1_chr3_179342709_179399936 | MFN1 | chr3 | 179342709 | 179399936 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0001 | c0001 | t0001 | g0043 | EUR | GBR | MFN1_chr3_179342709_179399936 | MFN1 | chr3 | 179342709 | 179399936 |
HG00099 | hp2 | a0001 | c0001 | t0001 | g0267 | EUR | GBR | MFN1_chr3_179342709_179399936 | MFN1 | chr3 | 179342709 | 179399936 |
HG00140 | hp1 | a0001 | c0001 | t0004 | g0001 | EUR | GBR | MFN1_chr3_179342709_179399936 | MFN1 | chr3 | 179342709 | 179399936 |
HG00140 | hp2 | a0001 | c0001 | t0002 | g0181 | EUR | GBR | MFN1_chr3_179342709_179399936 | MFN1 | chr3 | 179342709 | 179399936 |
HG00280 | hp1 | a0001 | c0001 | t0028 | g0185 | EUR | FIN | MFN1_chr3_179342709_179399936 | MFN1 | chr3 | 179342709 | 179399936 |
HG00280 | hp2 | a0001 | c0001 | t0014 | g0071 | EUR | FIN | MFN1_chr3_179342709_179399936 | MFN1 | chr3 | 179342709 | 179399936 |
HG00323 | hp1 | a0001 | c0001 | t0004 | g0079 | EUR | FIN | MFN1_chr3_179342709_179399936 | MFN1 | chr3 | 179342709 | 179399936 |
HG00323 | hp2 | a0001 | c0001 | t0014 | g0070 | EUR | FIN | MFN1_chr3_179342709_179399936 | MFN1 | chr3 | 179342709 | 179399936 |
HG00408 | hp1 | a0001 | c0001 | t0001 | g0237 | EAS | CHS | MFN1_chr3_179342709_179399936 | MFN1 | chr3 | 179342709 | 179399936 |
HG00408 | hp2 | a0001 | c0001 | t0024 | g0195 | EAS | CHS | MFN1_chr3_179342709_179399936 | MFN1 | chr3 | 179342709 | 179399936 |
HG00423 | hp1 | a0001 | c0001 | t0002 | g0167 | EAS | CHS | MFN1_chr3_179342709_179399936 | MFN1 | chr3 | 179342709 | 179399936 |
HG00423 | hp2 | a0001 | c0001 | t0031 | g0254 | EAS | CHS | MFN1_chr3_179342709_179399936 | MFN1 | chr3 | 179342709 | 179399936 |
HG00438 | hp1 | a0001 | c0001 | t0004 | g0001 | EAS | CHS | MFN1_chr3_179342709_179399936 | MFN1 | chr3 | 179342709 | 179399936 |
HG00438 | hp2 | a0001 | c0001 | t0001 | g0111 | EAS | CHS | MFN1_chr3_179342709_179399936 | MFN1 | chr3 | 179342709 | 179399936 |
HG00544 | hp1 | a0001 | c0001 | t0011 | g0186 | EAS | CHS | MFN1_chr3_179342709_179399936 | MFN1 | chr3 | 179342709 | 179399936 |
HG00544 | hp2 | a0001 | c0001 | t0001 | g0030 | EAS | CHS | MFN1_chr3_179342709_179399936 | MFN1 | chr3 | 179342709 | 179399936 |
HG00597 | hp1 | a0002 | c0003 | t0003 | g0236 | EAS | CHS | MFN1_chr3_179342709_179399936 | MFN1 | chr3 | 179342709 | 179399936 |
HG00597 | hp2 | a0001 | c0001 | t0001 | g0031 | EAS | CHS | MFN1_chr3_179342709_179399936 | MFN1 | chr3 | 179342709 | 179399936 |
HG00609 | hp1 | a0001 | c0001 | t0050 | g0233 | EAS | CHS | MFN1_chr3_179342709_179399936 | MFN1 | chr3 | 179342709 | 179399936 |
HG00609 | hp2 | a0001 | c0001 | t0044 | g0003 | EAS | CHS | MFN1_chr3_179342709_179399936 | MFN1 | chr3 | 179342709 | 179399936 |
HG00621 | hp1 | a0001 | c0001 | t0001 | g0031 | EAS | CHS | MFN1_chr3_179342709_179399936 | MFN1 | chr3 | 179342709 | 179399936 |
HG00621 | hp2 | a0001 | c0001 | t0010 | g0001 | EAS | CHS | MFN1_chr3_179342709_179399936 | MFN1 | chr3 | 179342709 | 179399936 |
HG00639 | hp1 | a0001 | c0001 | t0002 | g0190 | AMR | PUR | MFN1_chr3_179342709_179399936 | MFN1 | chr3 | 179342709 | 179399936 |
HG00639 | hp2 | a0001 | c0001 | t0001 | g0007 | AMR | PUR | MFN1_chr3_179342709_179399936 | MFN1 | chr3 | 179342709 | 179399936 |
HG00642 | hp1 | a0001 | c0001 | t0001 | g0232 | AMR | PUR | MFN1_chr3_179342709_179399936 | MFN1 | chr3 | 179342709 | 179399936 |
HG00642 | hp2 | a0001 | c0001 | t0003 | g0033 | AMR | PUR | MFN1_chr3_179342709_179399936 | MFN1 | chr3 | 179342709 | 179399936 |
HG00733 | hp1 | a0001 | c0001 | t0001 | g0043 | AMR | PUR | MFN1_chr3_179342709_179399936 | MFN1 | chr3 | 179342709 | 179399936 |
HG00733 | hp2 | a0001 | c0001 | t0007 | g0140 | AMR | PUR | MFN1_chr3_179342709_179399936 | MFN1 | chr3 | 179342709 | 179399936 |
HG00735 | hp1 | a0001 | c0001 | t0031 | g0132 | AMR | PUR | MFN1_chr3_179342709_179399936 | MFN1 | chr3 | 179342709 | 179399936 |
HG00735 | hp2 | a0001 | c0001 | t0012 | g0061 | AMR | PUR | MFN1_chr3_179342709_179399936 | MFN1 | chr3 | 179342709 | 179399936 |
HG00738 | hp1 | a0001 | c0001 | t0002 | g0159 | AMR | PUR | MFN1_chr3_179342709_179399936 | MFN1 | chr3 | 179342709 | 179399936 |
HG00738 | hp2 | a0001 | c0001 | t0001 | g0007 | AMR | PUR | MFN1_chr3_179342709_179399936 | MFN1 | chr3 | 179342709 | 179399936 |
HG00741 | hp1 | a0001 | c0001 | t0002 | g0178 | AMR | PUR | MFN1_chr3_179342709_179399936 | MFN1 | chr3 | 179342709 | 179399936 |
HG00741 | hp2 | a0001 | c0001 | t0001 | g0012 | AMR | PUR | MFN1_chr3_179342709_179399936 | MFN1 | chr3 | 179342709 | 179399936 |
HG01069 | hp1 | a0001 | c0001 | t0018 | g0022 | AMR | PUR | MFN1_chr3_179342709_179399936 | MFN1 | chr3 | 179342709 | 179399936 |
HG01069 | hp2 | a0001 | c0001 | t0025 | g0291 | AMR | PUR | MFN1_chr3_179342709_179399936 | MFN1 | chr3 | 179342709 | 179399936 |
HG01070 | hp1 | a0001 | c0001 | t0016 | g0080 | AMR | PUR | MFN1_chr3_179342709_179399936 | MFN1 | chr3 | 179342709 | 179399936 |
HG01070 | hp2 | a0001 | c0001 | t0013 | g0013 | AMR | PUR | MFN1_chr3_179342709_179399936 | MFN1 | chr3 | 179342709 | 179399936 |
HG01071 | hp1 | a0001 | c0001 | t0025 | g0020 | AMR | PUR | MFN1_chr3_179342709_179399936 | MFN1 | chr3 | 179342709 | 179399936 |
HG01071 | hp2 | a0001 | c0001 | t0016 | g0082 | AMR | PUR | MFN1_chr3_179342709_179399936 | MFN1 | chr3 | 179342709 | 179399936 |
HG01074 | hp1 | a0001 | c0001 | t0002 | g0211 | AMR | PUR | MFN1_chr3_179342709_179399936 | MFN1 | chr3 | 179342709 | 179399936 |
HG01074 | hp2 | a0001 | c0001 | t0001 | g0012 | AMR | PUR | MFN1_chr3_179342709_179399936 | MFN1 | chr3 | 179342709 | 179399936 |
HG01081 | hp1 | a0001 | c0001 | t0005 | g0161 | AMR | PUR | MFN1_chr3_179342709_179399936 | MFN1 | chr3 | 179342709 | 179399936 |
HG01081 | hp2 | a0001 | c0001 | t0001 | g0077 | AMR | PUR | MFN1_chr3_179342709_179399936 | MFN1 | chr3 | 179342709 | 179399936 |
HG01106 | hp1 | a0001 | c0001 | t0001 | g0078 | AMR | PUR | MFN1_chr3_179342709_179399936 | MFN1 | chr3 | 179342709 | 179399936 |
HG01106 | hp2 | a0001 | c0001 | t0001 | g0042 | AMR | PUR | MFN1_chr3_179342709_179399936 | MFN1 | chr3 | 179342709 | 179399936 |
HG01167 | hp1 | a0001 | c0001 | t0018 | g0053 | AMR | PUR | MFN1_chr3_179342709_179399936 | MFN1 | chr3 | 179342709 | 179399936 |
HG01167 | hp2 | a0001 | c0001 | t0015 | g0300 | AMR | PUR | MFN1_chr3_179342709_179399936 | MFN1 | chr3 | 179342709 | 179399936 |
HG01168 | hp1 | a0001 | c0001 | t0002 | g0006 | AMR | PUR | MFN1_chr3_179342709_179399936 | MFN1 | chr3 | 179342709 | 179399936 |
HG01168 | hp2 | a0001 | c0001 | t0001 | g0068 | AMR | PUR | MFN1_chr3_179342709_179399936 | MFN1 | chr3 | 179342709 | 179399936 |
HG01169 | hp1 | a0001 | c0001 | t0015 | g0299 | AMR | PUR | MFN1_chr3_179342709_179399936 | MFN1 | chr3 | 179342709 | 179399936 |
HG01169 | hp2 | a0001 | c0001 | t0001 | g0067 | AMR | PUR | MFN1_chr3_179342709_179399936 | MFN1 | chr3 | 179342709 | 179399936 |
HG01175 | hp1 | a0001 | c0001 | t0037 | g0293 | AMR | PUR | MFN1_chr3_179342709_179399936 | MFN1 | chr3 | 179342709 | 179399936 |
HG01175 | hp2 | a0001 | c0001 | t0002 | g0191 | AMR | PUR | MFN1_chr3_179342709_179399936 | MFN1 | chr3 | 179342709 | 179399936 |
HG01192 | hp1 | a0001 | c0001 | t0004 | g0096 | AMR | PUR | MFN1_chr3_179342709_179399936 | MFN1 | chr3 | 179342709 | 179399936 |
HG01192 | hp2 | a0001 | c0001 | t0001 | g0007 | AMR | PUR | MFN1_chr3_179342709_179399936 | MFN1 | chr3 | 179342709 | 179399936 |
HG01243 | hp1 | a0001 | c0001 | t0004 | g0086 | AMR | PUR | MFN1_chr3_179342709_179399936 | MFN1 | chr3 | 179342709 | 179399936 |
HG01243 | hp2 | a0001 | c0001 | t0002 | g0158 | AMR | PUR | MFN1_chr3_179342709_179399936 | MFN1 | chr3 | 179342709 | 179399936 |
HG01255 | hp1 | a0001 | c0001 | t0001 | g0004 | AMR | CLM | MFN1_chr3_179342709_179399936 | MFN1 | chr3 | 179342709 | 179399936 |
HG01255 | hp2 | a0001 | c0001 | t0002 | g0220 | AMR | CLM | MFN1_chr3_179342709_179399936 | MFN1 | chr3 | 179342709 | 179399936 |
HG01256 | hp1 | a0001 | c0001 | t0002 | g0006 | AMR | CLM | MFN1_chr3_179342709_179399936 | MFN1 | chr3 | 179342709 | 179399936 |
HG01256 | hp2 | a0001 | c0001 | t0003 | g0133 | AMR | CLM | MFN1_chr3_179342709_179399936 | MFN1 | chr3 | 179342709 | 179399936 |
HG01257 | hp1 | a0001 | c0001 | t0030 | g0013 | AMR | CLM | MFN1_chr3_179342709_179399936 | MFN1 | chr3 | 179342709 | 179399936 |
HG01257 | hp2 | a0001 | c0001 | t0011 | g0035 | AMR | CLM | MFN1_chr3_179342709_179399936 | MFN1 | chr3 | 179342709 | 179399936 |
HG01258 | hp1 | a0001 | c0001 | t0003 | g0137 | AMR | CLM | MFN1_chr3_179342709_179399936 | MFN1 | chr3 | 179342709 | 179399936 |
HG01258 | hp2 | a0001 | c0001 | t0013 | g0013 | AMR | CLM | MFN1_chr3_179342709_179399936 | MFN1 | chr3 | 179342709 | 179399936 |
HG01261 | hp1 | a0001 | c0001 | t0001 | g0151 | AMR | CLM | MFN1_chr3_179342709_179399936 | MFN1 | chr3 | 179342709 | 179399936 |
HG01261 | hp2 | a0001 | c0001 | t0032 | g0229 | AMR | CLM | MFN1_chr3_179342709_179399936 | MFN1 | chr3 | 179342709 | 179399936 |
HG01346 | hp1 | a0001 | c0001 | t0001 | g0019 | AMR | CLM | MFN1_chr3_179342709_179399936 | MFN1 | chr3 | 179342709 | 179399936 |
HG01346 | hp2 | a0001 | c0001 | t0002 | g0223 | AMR | CLM | MFN1_chr3_179342709_179399936 | MFN1 | chr3 | 179342709 | 179399936 |
HG01358 | hp1 | a0001 | c0001 | t0004 | g0001 | AMR | CLM | MFN1_chr3_179342709_179399936 | MFN1 | chr3 | 179342709 | 179399936 |
HG01358 | hp2 | a0001 | c0001 | t0001 | g0143 | AMR | CLM | MFN1_chr3_179342709_179399936 | MFN1 | chr3 | 179342709 | 179399936 |
HG01361 | hp1 | a0001 | c0001 | t0005 | g0017 | AMR | CLM | MFN1_chr3_179342709_179399936 | MFN1 | chr3 | 179342709 | 179399936 |
HG01361 | hp2 | a0001 | c0001 | t0001 | g0244 | AMR | CLM | MFN1_chr3_179342709_179399936 | MFN1 | chr3 | 179342709 | 179399936 |
HG01433 | hp1 | a0001 | c0001 | t0020 | g0101 | AMR | CLM | MFN1_chr3_179342709_179399936 | MFN1 | chr3 | 179342709 | 179399936 |
HG01433 | hp2 | a0001 | c0001 | t0012 | g0059 | AMR | CLM | MFN1_chr3_179342709_179399936 | MFN1 | chr3 | 179342709 | 179399936 |
HG01496 | hp1 | a0001 | c0001 | t0007 | g0258 | AMR | CLM | MFN1_chr3_179342709_179399936 | MFN1 | chr3 | 179342709 | 179399936 |
HG01496 | hp2 | a0001 | c0001 | t0001 | g0217 | AMR | CLM | MFN1_chr3_179342709_179399936 | MFN1 | chr3 | 179342709 | 179399936 |
HG01515 | hp1 | a0001 | c0001 | t0005 | g0203 | EUR | IBS | MFN1_chr3_179342709_179399936 | MFN1 | chr3 | 179342709 | 179399936 |
HG01515 | hp2 | a0001 | c0001 | t0004 | g0069 | EUR | IBS | MFN1_chr3_179342709_179399936 | MFN1 | chr3 | 179342709 | 179399936 |
HG01517 | hp1 | a0001 | c0001 | t0002 | g0204 | EUR | IBS | MFN1_chr3_179342709_179399936 | MFN1 | chr3 | 179342709 | 179399936 |
HG01517 | hp2 | a0001 | c0001 | t0007 | g0265 | EUR | IBS | MFN1_chr3_179342709_179399936 | MFN1 | chr3 | 179342709 | 179399936 |
HG01884 | hp1 | a0001 | c0001 | t0018 | g0022 | AFR | ACB | MFN1_chr3_179342709_179399936 | MFN1 | chr3 | 179342709 | 179399936 |
HG01884 | hp2 | a0001 | c0001 | t0001 | g0215 | AFR | ACB | MFN1_chr3_179342709_179399936 | MFN1 | chr3 | 179342709 | 179399936 |
HG01928 | hp1 | a0001 | c0001 | t0022 | g0014 | AMR | PEL | MFN1_chr3_179342709_179399936 | MFN1 | chr3 | 179342709 | 179399936 |
HG01928 | hp2 | a0001 | c0001 | t0013 | g0212 | AMR | PEL | MFN1_chr3_179342709_179399936 | MFN1 | chr3 | 179342709 | 179399936 |
HG01934 | hp1 | a0001 | c0001 | t0013 | g0013 | AMR | PEL | MFN1_chr3_179342709_179399936 | MFN1 | chr3 | 179342709 | 179399936 |
HG01934 | hp2 | a0001 | c0001 | t0002 | g0219 | AMR | PEL | MFN1_chr3_179342709_179399936 | MFN1 | chr3 | 179342709 | 179399936 |
HG01952 | hp1 | a0001 | c0001 | t0007 | g0088 | AMR | PEL | MFN1_chr3_179342709_179399936 | MFN1 | chr3 | 179342709 | 179399936 |
HG01952 | hp2 | a0001 | c0001 | t0011 | g0035 | AMR | PEL | MFN1_chr3_179342709_179399936 | MFN1 | chr3 | 179342709 | 179399936 |
HG01975 | hp1 | a0001 | c0001 | t0030 | g0224 | AMR | PEL | MFN1_chr3_179342709_179399936 | MFN1 | chr3 | 179342709 | 179399936 |
HG01975 | hp2 | a0001 | c0001 | t0002 | g0222 | AMR | PEL | MFN1_chr3_179342709_179399936 | MFN1 | chr3 | 179342709 | 179399936 |
HG01978 | hp1 | a0003 | c0006 | t0003 | g0245 | AMR | PEL | MFN1_chr3_179342709_179399936 | MFN1 | chr3 | 179342709 | 179399936 |
HG01978 | hp2 | a0001 | c0001 | t0008 | g0149 | AMR | PEL | MFN1_chr3_179342709_179399936 | MFN1 | chr3 | 179342709 | 179399936 |
HG01981 | hp1 | a0001 | c0001 | t0005 | g0038 | AMR | PEL | MFN1_chr3_179342709_179399936 | MFN1 | chr3 | 179342709 | 179399936 |
HG01981 | hp2 | a0001 | c0001 | t0013 | g0214 | AMR | PEL | MFN1_chr3_179342709_179399936 | MFN1 | chr3 | 179342709 | 179399936 |
HG01993 | hp1 | a0001 | c0001 | t0002 | g0218 | AMR | PEL | MFN1_chr3_179342709_179399936 | MFN1 | chr3 | 179342709 | 179399936 |
HG01993 | hp2 | a0001 | c0001 | t0014 | g0072 | AMR | PEL | MFN1_chr3_179342709_179399936 | MFN1 | chr3 | 179342709 | 179399936 |
HG02015 | hp1 | a0001 | c0001 | t0001 | g0008 | EAS | KHV | MFN1_chr3_179342709_179399936 | MFN1 | chr3 | 179342709 | 179399936 |
HG02015 | hp2 | a0001 | c0001 | t0005 | g0162 | EAS | KHV | MFN1_chr3_179342709_179399936 | MFN1 | chr3 | 179342709 | 179399936 |
HG02027 | hp1 | a0001 | c0001 | t0001 | g0123 | EAS | KHV | MFN1_chr3_179342709_179399936 | MFN1 | chr3 | 179342709 | 179399936 |
HG02027 | hp2 | a0001 | c0001 | t0001 | g0008 | EAS | KHV | MFN1_chr3_179342709_179399936 | MFN1 | chr3 | 179342709 | 179399936 |
HG02055 | hp1 | a0001 | c0001 | t0001 | g0273 | AFR | ACB | MFN1_chr3_179342709_179399936 | MFN1 | chr3 | 179342709 | 179399936 |
HG02055 | hp2 | a0001 | c0001 | t0012 | g0097 | AFR | ACB | MFN1_chr3_179342709_179399936 | MFN1 | chr3 | 179342709 | 179399936 |
HG02056 | hp1 | a0001 | c0001 | t0001 | g0040 | EAS | KHV | MFN1_chr3_179342709_179399936 | MFN1 | chr3 | 179342709 | 179399936 |
HG02056 | hp2 | a0001 | c0001 | t0003 | g0117 | EAS | KHV | MFN1_chr3_179342709_179399936 | MFN1 | chr3 | 179342709 | 179399936 |
HG02071 | hp1 | a0001 | c0001 | t0001 | g0010 | EAS | KHV | MFN1_chr3_179342709_179399936 | MFN1 | chr3 | 179342709 | 179399936 |
HG02071 | hp2 | a0001 | c0001 | t0005 | g0207 | EAS | KHV | MFN1_chr3_179342709_179399936 | MFN1 | chr3 | 179342709 | 179399936 |
HG02074 | hp1 | a0001 | c0001 | t0001 | g0010 | EAS | KHV | MFN1_chr3_179342709_179399936 | MFN1 | chr3 | 179342709 | 179399936 |
HG02074 | hp2 | a0001 | c0001 | t0011 | g0200 | EAS | KHV | MFN1_chr3_179342709_179399936 | MFN1 | chr3 | 179342709 | 179399936 |
HG02080 | hp1 | a0001 | c0001 | t0001 | g0238 | EAS | KHV | MFN1_chr3_179342709_179399936 | MFN1 | chr3 | 179342709 | 179399936 |
HG02080 | hp2 | a0001 | c0001 | t0024 | g0201 | EAS | KHV | MFN1_chr3_179342709_179399936 | MFN1 | chr3 | 179342709 | 179399936 |
HG02083 | hp1 | a0001 | c0001 | t0005 | g0183 | EAS | KHV | MFN1_chr3_179342709_179399936 | MFN1 | chr3 | 179342709 | 179399936 |
HG02083 | hp2 | a0001 | c0001 | t0001 | g0116 | EAS | KHV | MFN1_chr3_179342709_179399936 | MFN1 | chr3 | 179342709 | 179399936 |
HG02132 | hp1 | a0001 | c0001 | t0001 | g0040 | EAS | KHV | MFN1_chr3_179342709_179399936 | MFN1 | chr3 | 179342709 | 179399936 |
HG02132 | hp2 | a0001 | c0001 | t0001 | g0112 | EAS | KHV | MFN1_chr3_179342709_179399936 | MFN1 | chr3 | 179342709 | 179399936 |
HG02145 | hp1 | a0001 | c0001 | t0001 | g0144 | AFR | ACB | MFN1_chr3_179342709_179399936 | MFN1 | chr3 | 179342709 | 179399936 |
HG02145 | hp2 | a0001 | c0001 | t0018 | g0050 | AFR | ACB | MFN1_chr3_179342709_179399936 | MFN1 | chr3 | 179342709 | 179399936 |
HG02148 | hp1 | a0001 | c0001 | t0014 | g0014 | AMR | PEL | MFN1_chr3_179342709_179399936 | MFN1 | chr3 | 179342709 | 179399936 |
HG02148 | hp2 | a0001 | c0001 | t0002 | g0038 | AMR | PEL | MFN1_chr3_179342709_179399936 | MFN1 | chr3 | 179342709 | 179399936 |
HG02155 | hp1 | a0001 | c0001 | t0001 | g0251 | EAS | CDX | MFN1_chr3_179342709_179399936 | MFN1 | chr3 | 179342709 | 179399936 |
HG02155 | hp2 | a0001 | c0001 | t0001 | g0114 | EAS | CDX | MFN1_chr3_179342709_179399936 | MFN1 | chr3 | 179342709 | 179399936 |
HG02165 | hp1 | a0001 | c0001 | t0011 | g0187 | EAS | CDX | MFN1_chr3_179342709_179399936 | MFN1 | chr3 | 179342709 | 179399936 |
HG02165 | hp2 | a0001 | c0001 | t0004 | g0001 | EAS | CDX | MFN1_chr3_179342709_179399936 | MFN1 | chr3 | 179342709 | 179399936 |
HG02257 | hp1 | a0001 | c0001 | t0023 | g0304 | AFR | ACB | MFN1_chr3_179342709_179399936 | MFN1 | chr3 | 179342709 | 179399936 |
HG02257 | hp2 | a0001 | c0001 | t0009 | g0025 | AFR | ACB | MFN1_chr3_179342709_179399936 | MFN1 | chr3 | 179342709 | 179399936 |
HG02258 | hp1 | a0001 | c0001 | t0042 | g0032 | AFR | ACB | MFN1_chr3_179342709_179399936 | MFN1 | chr3 | 179342709 | 179399936 |
HG02258 | hp2 | a0001 | c0001 | t0006 | g0047 | AFR | ACB | MFN1_chr3_179342709_179399936 | MFN1 | chr3 | 179342709 | 179399936 |
HG02273 | hp1 | a0001 | c0001 | t0001 | g0239 | AMR | PEL | MFN1_chr3_179342709_179399936 | MFN1 | chr3 | 179342709 | 179399936 |
HG02273 | hp2 | a0001 | c0001 | t0014 | g0014 | AMR | PEL | MFN1_chr3_179342709_179399936 | MFN1 | chr3 | 179342709 | 179399936 |
HG02280 | hp1 | a0001 | c0001 | t0020 | g0102 | AFR | ACB | MFN1_chr3_179342709_179399936 | MFN1 | chr3 | 179342709 | 179399936 |
HG02280 | hp2 | a0001 | c0001 | t0002 | g0194 | AFR | ACB | MFN1_chr3_179342709_179399936 | MFN1 | chr3 | 179342709 | 179399936 |
HG02293 | hp1 | a0001 | c0001 | t0002 | g0221 | AMR | PEL | MFN1_chr3_179342709_179399936 | MFN1 | chr3 | 179342709 | 179399936 |
HG02293 | hp2 | a0001 | c0001 | t0001 | g0016 | AMR | PEL | MFN1_chr3_179342709_179399936 | MFN1 | chr3 | 179342709 | 179399936 |
HG02300 | hp1 | a0001 | c0001 | t0001 | g0007 | AMR | PEL | MFN1_chr3_179342709_179399936 | MFN1 | chr3 | 179342709 | 179399936 |
HG02300 | hp2 | a0001 | c0001 | t0013 | g0213 | AMR | PEL | MFN1_chr3_179342709_179399936 | MFN1 | chr3 | 179342709 | 179399936 |
HG02572 | hp1 | a0001 | c0001 | t0005 | g0098 | AFR | GWD | MFN1_chr3_179342709_179399936 | MFN1 | chr3 | 179342709 | 179399936 |
HG02572 | hp2 | a0001 | c0001 | t0009 | g0057 | AFR | GWD | MFN1_chr3_179342709_179399936 | MFN1 | chr3 | 179342709 | 179399936 |
HG02602 | hp1 | a0001 | c0001 | t0007 | g0248 | SAS | PJL | MFN1_chr3_179342709_179399936 | MFN1 | chr3 | 179342709 | 179399936 |
HG02602 | hp2 | a0001 | c0001 | t0017 | g0095 | SAS | PJL | MFN1_chr3_179342709_179399936 | MFN1 | chr3 | 179342709 | 179399936 |
HG02615 | hp1 | a0001 | c0001 | t0015 | g0021 | AFR | GWD | MFN1_chr3_179342709_179399936 | MFN1 | chr3 | 179342709 | 179399936 |
HG02615 | hp2 | a0001 | c0001 | t0026 | g0047 | AFR | GWD | MFN1_chr3_179342709_179399936 | MFN1 | chr3 | 179342709 | 179399936 |
HG02622 | hp1 | a0001 | c0001 | t0006 | g0298 | AFR | GWD | MFN1_chr3_179342709_179399936 | MFN1 | chr3 | 179342709 | 179399936 |
HG02622 | hp2 | a0001 | c0001 | t0001 | g0045 | AFR | GWD | MFN1_chr3_179342709_179399936 | MFN1 | chr3 | 179342709 | 179399936 |
HG02630 | hp1 | a0001 | c0001 | t0051 | g0252 | AFR | GWD | MFN1_chr3_179342709_179399936 | MFN1 | chr3 | 179342709 | 179399936 |
HG02630 | hp2 | a0001 | c0001 | t0009 | g0065 | AFR | GWD | MFN1_chr3_179342709_179399936 | MFN1 | chr3 | 179342709 | 179399936 |
HG02647 | hp1 | a0001 | c0001 | t0035 | g0103 | AFR | GWD | MFN1_chr3_179342709_179399936 | MFN1 | chr3 | 179342709 | 179399936 |
HG02647 | hp2 | a0001 | c0001 | t0033 | g0004 | AFR | GWD | MFN1_chr3_179342709_179399936 | MFN1 | chr3 | 179342709 | 179399936 |
HG02683 | hp1 | a0001 | c0001 | t0022 | g0073 | SAS | PJL | MFN1_chr3_179342709_179399936 | MFN1 | chr3 | 179342709 | 179399936 |
HG02683 | hp2 | a0001 | c0001 | t0005 | g0180 | SAS | PJL | MFN1_chr3_179342709_179399936 | MFN1 | chr3 | 179342709 | 179399936 |
HG02698 | hp1 | a0001 | c0001 | t0001 | g0002 | SAS | PJL | MFN1_chr3_179342709_179399936 | MFN1 | chr3 | 179342709 | 179399936 |
HG02698 | hp2 | a0001 | c0001 | t0005 | g0006 | SAS | PJL | MFN1_chr3_179342709_179399936 | MFN1 | chr3 | 179342709 | 179399936 |
HG02717 | hp1 | a0001 | c0001 | t0012 | g0023 | AFR | GWD | MFN1_chr3_179342709_179399936 | MFN1 | chr3 | 179342709 | 179399936 |
HG02717 | hp2 | a0001 | c0001 | t0034 | g0051 | AFR | GWD | MFN1_chr3_179342709_179399936 | MFN1 | chr3 | 179342709 | 179399936 |
HG02735 | hp1 | a0001 | c0001 | t0001 | g0243 | SAS | PJL | MFN1_chr3_179342709_179399936 | MFN1 | chr3 | 179342709 | 179399936 |
HG02735 | hp2 | a0001 | c0001 | t0004 | g0089 | SAS | PJL | MFN1_chr3_179342709_179399936 | MFN1 | chr3 | 179342709 | 179399936 |
HG02738 | hp1 | a0001 | c0001 | t0017 | g0094 | SAS | PJL | MFN1_chr3_179342709_179399936 | MFN1 | chr3 | 179342709 | 179399936 |
HG02738 | hp2 | a0001 | c0001 | t0002 | g0184 | SAS | PJL | MFN1_chr3_179342709_179399936 | MFN1 | chr3 | 179342709 | 179399936 |
HG02809 | hp1 | a0001 | c0001 | t0041 | g0032 | AFR | GWD | MFN1_chr3_179342709_179399936 | MFN1 | chr3 | 179342709 | 179399936 |
HG02809 | hp2 | a0001 | c0001 | t0015 | g0021 | AFR | GWD | MFN1_chr3_179342709_179399936 | MFN1 | chr3 | 179342709 | 179399936 |
HG02818 | hp1 | a0001 | c0001 | t0009 | g0024 | AFR | GWD | MFN1_chr3_179342709_179399936 | MFN1 | chr3 | 179342709 | 179399936 |
HG02818 | hp2 | a0001 | c0001 | t0026 | g0100 | AFR | GWD | MFN1_chr3_179342709_179399936 | MFN1 | chr3 | 179342709 | 179399936 |
HG02886 | hp1 | a0001 | c0001 | t0001 | g0142 | AFR | GWD | MFN1_chr3_179342709_179399936 | MFN1 | chr3 | 179342709 | 179399936 |
HG02886 | hp2 | a0001 | c0001 | t0017 | g0039 | AFR | GWD | MFN1_chr3_179342709_179399936 | MFN1 | chr3 | 179342709 | 179399936 |
HG02895 | hp1 | a0001 | c0001 | t0006 | g0009 | AFR | GWD | MFN1_chr3_179342709_179399936 | MFN1 | chr3 | 179342709 | 179399936 |
HG02895 | hp2 | a0001 | c0001 | t0006 | g0009 | AFR | GWD | MFN1_chr3_179342709_179399936 | MFN1 | chr3 | 179342709 | 179399936 |
HG02896 | hp1 | a0001 | c0001 | t0019 | g0106 | AFR | GWD | MFN1_chr3_179342709_179399936 | MFN1 | chr3 | 179342709 | 179399936 |
HG02896 | hp2 | a0001 | c0001 | t0001 | g0141 | AFR | GWD | MFN1_chr3_179342709_179399936 | MFN1 | chr3 | 179342709 | 179399936 |
HG02897 | hp1 | a0001 | c0001 | t0006 | g0292 | AFR | GWD | MFN1_chr3_179342709_179399936 | MFN1 | chr3 | 179342709 | 179399936 |
HG02897 | hp2 | a0001 | c0001 | t0001 | g0004 | AFR | GWD | MFN1_chr3_179342709_179399936 | MFN1 | chr3 | 179342709 | 179399936 |
HG02922 | hp1 | a0001 | c0001 | t0012 | g0056 | AFR | ESN | MFN1_chr3_179342709_179399936 | MFN1 | chr3 | 179342709 | 179399936 |
HG02922 | hp2 | a0001 | c0001 | t0021 | g0009 | AFR | ESN | MFN1_chr3_179342709_179399936 | MFN1 | chr3 | 179342709 | 179399936 |
HG02965 | hp1 | a0001 | c0001 | t0019 | g0054 | AFR | ESN | MFN1_chr3_179342709_179399936 | MFN1 | chr3 | 179342709 | 179399936 |
HG02965 | hp2 | a0001 | c0001 | t0021 | g0009 | AFR | ESN | MFN1_chr3_179342709_179399936 | MFN1 | chr3 | 179342709 | 179399936 |
HG02970 | hp1 | a0001 | c0001 | t0001 | g0134 | AFR | ESN | MFN1_chr3_179342709_179399936 | MFN1 | chr3 | 179342709 | 179399936 |
HG02970 | hp2 | a0001 | c0001 | t0001 | g0018 | AFR | ESN | MFN1_chr3_179342709_179399936 | MFN1 | chr3 | 179342709 | 179399936 |
HG02976 | hp1 | a0001 | c0001 | t0036 | g0210 | AFR | ESN | MFN1_chr3_179342709_179399936 | MFN1 | chr3 | 179342709 | 179399936 |
HG02976 | hp2 | a0001 | c0001 | t0020 | g0216 | AFR | ESN | MFN1_chr3_179342709_179399936 | MFN1 | chr3 | 179342709 | 179399936 |
HG03017 | hp1 | a0001 | c0001 | t0002 | g0006 | SAS | PJL | MFN1_chr3_179342709_179399936 | MFN1 | chr3 | 179342709 | 179399936 |
HG03017 | hp2 | a0001 | c0001 | t0001 | g0007 | SAS | PJL | MFN1_chr3_179342709_179399936 | MFN1 | chr3 | 179342709 | 179399936 |
HG03041 | hp1 | a0001 | c0001 | t0034 | g0055 | AFR | GWD | MFN1_chr3_179342709_179399936 | MFN1 | chr3 | 179342709 | 179399936 |
HG03041 | hp2 | a0001 | c0001 | t0006 | g0020 | AFR | GWD | MFN1_chr3_179342709_179399936 | MFN1 | chr3 | 179342709 | 179399936 |
HG03098 | hp1 | a0001 | c0001 | t0009 | g0062 | AFR | MSL | MFN1_chr3_179342709_179399936 | MFN1 | chr3 | 179342709 | 179399936 |
HG03098 | hp2 | a0001 | c0001 | t0006 | g0295 | AFR | MSL | MFN1_chr3_179342709_179399936 | MFN1 | chr3 | 179342709 | 179399936 |
HG03130 | hp1 | a0004 | c0007 | t0012 | g0023 | AFR | ESN | MFN1_chr3_179342709_179399936 | MFN1 | chr3 | 179342709 | 179399936 |
HG03130 | hp2 | a0001 | c0001 | t0001 | g0138 | AFR | ESN | MFN1_chr3_179342709_179399936 | MFN1 | chr3 | 179342709 | 179399936 |
HG03139 | hp1 | a0001 | c0001 | t0009 | g0025 | AFR | ESN | MFN1_chr3_179342709_179399936 | MFN1 | chr3 | 179342709 | 179399936 |
HG03139 | hp2 | a0001 | c0001 | t0001 | g0018 | AFR | ESN | MFN1_chr3_179342709_179399936 | MFN1 | chr3 | 179342709 | 179399936 |
HG03195 | hp1 | a0001 | c0001 | t0045 | g0024 | AFR | ESN | MFN1_chr3_179342709_179399936 | MFN1 | chr3 | 179342709 | 179399936 |
HG03195 | hp2 | a0001 | c0001 | t0052 | g0227 | AFR | ESN | MFN1_chr3_179342709_179399936 | MFN1 | chr3 | 179342709 | 179399936 |
HG03209 | hp1 | a0001 | c0001 | t0006 | g0048 | AFR | MSL | MFN1_chr3_179342709_179399936 | MFN1 | chr3 | 179342709 | 179399936 |
HG03209 | hp2 | a0001 | c0001 | t0006 | g0290 | AFR | MSL | MFN1_chr3_179342709_179399936 | MFN1 | chr3 | 179342709 | 179399936 |
HG03225 | hp1 | a0001 | c0001 | t0017 | g0090 | AFR | MSL | MFN1_chr3_179342709_179399936 | MFN1 | chr3 | 179342709 | 179399936 |
HG03225 | hp2 | a0001 | c0001 | t0033 | g0004 | AFR | MSL | MFN1_chr3_179342709_179399936 | MFN1 | chr3 | 179342709 | 179399936 |
HG03239 | hp1 | a0001 | c0001 | t0007 | g0274 | SAS | PJL | MFN1_chr3_179342709_179399936 | MFN1 | chr3 | 179342709 | 179399936 |
HG03239 | hp2 | a0001 | c0001 | t0003 | g0136 | SAS | PJL | MFN1_chr3_179342709_179399936 | MFN1 | chr3 | 179342709 | 179399936 |
HG03453 | hp1 | a0001 | c0009 | t0039 | g0225 | AFR | MSL | MFN1_chr3_179342709_179399936 | MFN1 | chr3 | 179342709 | 179399936 |
HG03453 | hp2 | a0001 | c0001 | t0017 | g0039 | AFR | MSL | MFN1_chr3_179342709_179399936 | MFN1 | chr3 | 179342709 | 179399936 |
HG03486 | hp1 | a0001 | c0001 | t0004 | g0091 | AFR | MSL | MFN1_chr3_179342709_179399936 | MFN1 | chr3 | 179342709 | 179399936 |
HG03486 | hp2 | a0001 | c0001 | t0009 | g0064 | AFR | MSL | MFN1_chr3_179342709_179399936 | MFN1 | chr3 | 179342709 | 179399936 |
HG03490 | hp1 | a0001 | c0001 | t0038 | g0294 | SAS | PJL | MFN1_chr3_179342709_179399936 | MFN1 | chr3 | 179342709 | 179399936 |
HG03490 | hp2 | a0001 | c0001 | t0001 | g0046 | SAS | PJL | MFN1_chr3_179342709_179399936 | MFN1 | chr3 | 179342709 | 179399936 |
HG03492 | hp1 | a0001 | c0001 | t0001 | g0046 | SAS | PJL | MFN1_chr3_179342709_179399936 | MFN1 | chr3 | 179342709 | 179399936 |
HG03492 | hp2 | a0001 | c0001 | t0001 | g0002 | SAS | PJL | MFN1_chr3_179342709_179399936 | MFN1 | chr3 | 179342709 | 179399936 |
HG03516 | hp1 | a0001 | c0001 | t0013 | g0135 | AFR | ESN | MFN1_chr3_179342709_179399936 | MFN1 | chr3 | 179342709 | 179399936 |
HG03516 | hp2 | a0001 | c0001 | t0009 | g0063 | AFR | ESN | MFN1_chr3_179342709_179399936 | MFN1 | chr3 | 179342709 | 179399936 |
HG03540 | hp1 | a0001 | c0001 | t0001 | g0250 | AFR | GWD | MFN1_chr3_179342709_179399936 | MFN1 | chr3 | 179342709 | 179399936 |
HG03540 | hp2 | a0005 | c0010 | t0032 | g0208 | AFR | GWD | MFN1_chr3_179342709_179399936 | MFN1 | chr3 | 179342709 | 179399936 |
HG03579 | hp1 | a0001 | c0001 | t0018 | g0052 | AFR | MSL | MFN1_chr3_179342709_179399936 | MFN1 | chr3 | 179342709 | 179399936 |
HG03579 | hp2 | a0001 | c0001 | t0003 | g0045 | AFR | MSL | MFN1_chr3_179342709_179399936 | MFN1 | chr3 | 179342709 | 179399936 |
HG03654 | hp1 | a0001 | c0001 | t0003 | g0253 | SAS | PJL | MFN1_chr3_179342709_179399936 | MFN1 | chr3 | 179342709 | 179399936 |
HG03654 | hp2 | a0001 | c0001 | t0001 | g0002 | SAS | PJL | MFN1_chr3_179342709_179399936 | MFN1 | chr3 | 179342709 | 179399936 |
HG03669 | hp1 | a0001 | c0002 | t0016 | g0286 | SAS | PJL | MFN1_chr3_179342709_179399936 | MFN1 | chr3 | 179342709 | 179399936 |
HG03669 | hp2 | a0001 | c0001 | t0001 | g0016 | SAS | PJL | MFN1_chr3_179342709_179399936 | MFN1 | chr3 | 179342709 | 179399936 |
HG03688 | hp1 | a0001 | c0001 | t0005 | g0148 | SAS | STU | MFN1_chr3_179342709_179399936 | MFN1 | chr3 | 179342709 | 179399936 |
HG03688 | hp2 | a0001 | c0002 | t0016 | g0284 | SAS | STU | MFN1_chr3_179342709_179399936 | MFN1 | chr3 | 179342709 | 179399936 |
HG03704 | hp1 | a0001 | c0002 | t0016 | g0283 | SAS | PJL | MFN1_chr3_179342709_179399936 | MFN1 | chr3 | 179342709 | 179399936 |
HG03704 | hp2 | a0001 | c0001 | t0001 | g0012 | SAS | PJL | MFN1_chr3_179342709_179399936 | MFN1 | chr3 | 179342709 | 179399936 |
HG03710 | hp1 | a0001 | c0001 | t0014 | g0074 | SAS | PJL | MFN1_chr3_179342709_179399936 | MFN1 | chr3 | 179342709 | 179399936 |
HG03710 | hp2 | a0001 | c0001 | t0002 | g0017 | SAS | PJL | MFN1_chr3_179342709_179399936 | MFN1 | chr3 | 179342709 | 179399936 |
HG03831 | hp1 | a0001 | c0001 | t0004 | g0085 | SAS | BEB | MFN1_chr3_179342709_179399936 | MFN1 | chr3 | 179342709 | 179399936 |
HG03831 | hp2 | a0001 | c0001 | t0001 | g0146 | SAS | BEB | MFN1_chr3_179342709_179399936 | MFN1 | chr3 | 179342709 | 179399936 |
HG03834 | hp1 | a0001 | c0001 | t0017 | g0093 | SAS | BEB | MFN1_chr3_179342709_179399936 | MFN1 | chr3 | 179342709 | 179399936 |
HG03834 | hp2 | a0001 | c0001 | t0001 | g0002 | SAS | BEB | MFN1_chr3_179342709_179399936 | MFN1 | chr3 | 179342709 | 179399936 |
HG03927 | hp1 | a0001 | c0001 | t0001 | g0152 | SAS | BEB | MFN1_chr3_179342709_179399936 | MFN1 | chr3 | 179342709 | 179399936 |
HG03927 | hp2 | a0001 | c0001 | t0014 | g0076 | SAS | BEB | MFN1_chr3_179342709_179399936 | MFN1 | chr3 | 179342709 | 179399936 |
HG03942 | hp1 | a0001 | c0002 | t0004 | g0282 | SAS | BEB | MFN1_chr3_179342709_179399936 | MFN1 | chr3 | 179342709 | 179399936 |
HG03942 | hp2 | a0001 | c0001 | t0022 | g0075 | SAS | BEB | MFN1_chr3_179342709_179399936 | MFN1 | chr3 | 179342709 | 179399936 |
HG04115 | hp1 | a0001 | c0001 | t0001 | g0264 | SAS | STU | MFN1_chr3_179342709_179399936 | MFN1 | chr3 | 179342709 | 179399936 |
HG04115 | hp2 | a0001 | c0001 | t0043 | g0206 | SAS | STU | MFN1_chr3_179342709_179399936 | MFN1 | chr3 | 179342709 | 179399936 |
HG04204 | hp1 | a0001 | c0001 | t0005 | g0176 | SAS | STU | MFN1_chr3_179342709_179399936 | MFN1 | chr3 | 179342709 | 179399936 |
HG04204 | hp2 | a0001 | c0001 | t0001 | g0145 | SAS | STU | MFN1_chr3_179342709_179399936 | MFN1 | chr3 | 179342709 | 179399936 |
HG04228 | hp1 | a0001 | c0001 | t0001 | g0049 | SAS | STU | MFN1_chr3_179342709_179399936 | MFN1 | chr3 | 179342709 | 179399936 |
HG04228 | hp2 | a0001 | c0002 | t0016 | g0281 | SAS | STU | MFN1_chr3_179342709_179399936 | MFN1 | chr3 | 179342709 | 179399936 |
NA18522 | hp1 | a0001 | c0001 | t0006 | g0297 | AFR | YRI | MFN1_chr3_179342709_179399936 | MFN1 | chr3 | 179342709 | 179399936 |
NA18522 | hp2 | a0001 | c0001 | t0001 | g0018 | AFR | YRI | MFN1_chr3_179342709_179399936 | MFN1 | chr3 | 179342709 | 179399936 |
NA18612 | hp1 | a0001 | c0001 | t0004 | g0026 | EAS | CHB | MFN1_chr3_179342709_179399936 | MFN1 | chr3 | 179342709 | 179399936 |
NA18612 | hp2 | a0001 | c0001 | t0001 | g0130 | EAS | CHB | MFN1_chr3_179342709_179399936 | MFN1 | chr3 | 179342709 | 179399936 |
NA18906 | hp1 | a0001 | c0001 | t0006 | g0020 | AFR | YRI | MFN1_chr3_179342709_179399936 | MFN1 | chr3 | 179342709 | 179399936 |
NA18906 | hp2 | a0001 | c0001 | t0009 | g0066 | AFR | YRI | MFN1_chr3_179342709_179399936 | MFN1 | chr3 | 179342709 | 179399936 |
NA18939 | hp1 | a0001 | c0001 | t0001 | g0107 | EAS | JPT | MFN1_chr3_179342709_179399936 | MFN1 | chr3 | 179342709 | 179399936 |
NA18939 | hp2 | a0001 | c0001 | t0005 | g0003 | EAS | JPT | MFN1_chr3_179342709_179399936 | MFN1 | chr3 | 179342709 | 179399936 |
NA18940 | hp1 | a0001 | c0001 | t0001 | g0126 | EAS | JPT | MFN1_chr3_179342709_179399936 | MFN1 | chr3 | 179342709 | 179399936 |
NA18940 | hp2 | a0001 | c0001 | t0002 | g0205 | EAS | JPT | MFN1_chr3_179342709_179399936 | MFN1 | chr3 | 179342709 | 179399936 |
NA18942 | hp1 | a0001 | c0001 | t0004 | g0001 | EAS | JPT | MFN1_chr3_179342709_179399936 | MFN1 | chr3 | 179342709 | 179399936 |
NA18942 | hp2 | a0001 | c0001 | t0001 | g0015 | EAS | JPT | MFN1_chr3_179342709_179399936 | MFN1 | chr3 | 179342709 | 179399936 |
NA18943 | hp1 | a0001 | c0001 | t0001 | g0125 | EAS | JPT | MFN1_chr3_179342709_179399936 | MFN1 | chr3 | 179342709 | 179399936 |
NA18943 | hp2 | a0001 | c0001 | t0001 | g0260 | EAS | JPT | MFN1_chr3_179342709_179399936 | MFN1 | chr3 | 179342709 | 179399936 |
NA18945 | hp1 | a0001 | c0001 | t0001 | g0118 | EAS | JPT | MFN1_chr3_179342709_179399936 | MFN1 | chr3 | 179342709 | 179399936 |
NA18945 | hp2 | a0001 | c0001 | t0008 | g0037 | EAS | JPT | MFN1_chr3_179342709_179399936 | MFN1 | chr3 | 179342709 | 179399936 |
NA18946 | hp1 | a0001 | c0001 | t0010 | g0084 | EAS | JPT | MFN1_chr3_179342709_179399936 | MFN1 | chr3 | 179342709 | 179399936 |
NA18946 | hp2 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | MFN1_chr3_179342709_179399936 | MFN1 | chr3 | 179342709 | 179399936 |
NA18947 | hp1 | a0001 | c0001 | t0002 | g0168 | EAS | JPT | MFN1_chr3_179342709_179399936 | MFN1 | chr3 | 179342709 | 179399936 |
NA18947 | hp2 | a0001 | c0001 | t0029 | g0029 | EAS | JPT | MFN1_chr3_179342709_179399936 | MFN1 | chr3 | 179342709 | 179399936 |
NA18949 | hp1 | a0001 | c0001 | t0001 | g0278 | EAS | JPT | MFN1_chr3_179342709_179399936 | MFN1 | chr3 | 179342709 | 179399936 |
NA18949 | hp2 | a0001 | c0001 | t0001 | g0266 | EAS | JPT | MFN1_chr3_179342709_179399936 | MFN1 | chr3 | 179342709 | 179399936 |
NA18951 | hp1 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | MFN1_chr3_179342709_179399936 | MFN1 | chr3 | 179342709 | 179399936 |
NA18951 | hp2 | a0001 | c0001 | t0001 | g0030 | EAS | JPT | MFN1_chr3_179342709_179399936 | MFN1 | chr3 | 179342709 | 179399936 |
NA18952 | hp1 | a0001 | c0001 | t0007 | g0019 | EAS | JPT | MFN1_chr3_179342709_179399936 | MFN1 | chr3 | 179342709 | 179399936 |
NA18952 | hp2 | a0001 | c0001 | t0010 | g0001 | EAS | JPT | MFN1_chr3_179342709_179399936 | MFN1 | chr3 | 179342709 | 179399936 |
NA18953 | hp1 | a0001 | c0001 | t0001 | g0131 | EAS | JPT | MFN1_chr3_179342709_179399936 | MFN1 | chr3 | 179342709 | 179399936 |
NA18953 | hp2 | a0001 | c0001 | t0010 | g0027 | EAS | JPT | MFN1_chr3_179342709_179399936 | MFN1 | chr3 | 179342709 | 179399936 |
NA18956 | hp1 | a0001 | c0001 | t0003 | g0011 | EAS | JPT | MFN1_chr3_179342709_179399936 | MFN1 | chr3 | 179342709 | 179399936 |
NA18956 | hp2 | a0001 | c0001 | t0008 | g0199 | EAS | JPT | MFN1_chr3_179342709_179399936 | MFN1 | chr3 | 179342709 | 179399936 |
NA18960 | hp1 | a0001 | c0001 | t0001 | g0150 | EAS | JPT | MFN1_chr3_179342709_179399936 | MFN1 | chr3 | 179342709 | 179399936 |
NA18960 | hp2 | a0001 | c0001 | t0001 | g0034 | EAS | JPT | MFN1_chr3_179342709_179399936 | MFN1 | chr3 | 179342709 | 179399936 |
NA18961 | hp1 | a0001 | c0001 | t0001 | g0276 | EAS | JPT | MFN1_chr3_179342709_179399936 | MFN1 | chr3 | 179342709 | 179399936 |
NA18961 | hp2 | a0001 | c0001 | t0001 | g0109 | EAS | JPT | MFN1_chr3_179342709_179399936 | MFN1 | chr3 | 179342709 | 179399936 |
NA18962 | hp1 | a0001 | c0001 | t0001 | g0242 | EAS | JPT | MFN1_chr3_179342709_179399936 | MFN1 | chr3 | 179342709 | 179399936 |
NA18962 | hp2 | a0001 | c0001 | t0002 | g0006 | EAS | JPT | MFN1_chr3_179342709_179399936 | MFN1 | chr3 | 179342709 | 179399936 |
NA18963 | hp1 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | MFN1_chr3_179342709_179399936 | MFN1 | chr3 | 179342709 | 179399936 |
NA18963 | hp2 | a0001 | c0001 | t0004 | g0083 | EAS | JPT | MFN1_chr3_179342709_179399936 | MFN1 | chr3 | 179342709 | 179399936 |
NA18964 | hp1 | a0001 | c0001 | t0001 | g0041 | EAS | JPT | MFN1_chr3_179342709_179399936 | MFN1 | chr3 | 179342709 | 179399936 |
NA18964 | hp2 | a0001 | c0001 | t0001 | g0113 | EAS | JPT | MFN1_chr3_179342709_179399936 | MFN1 | chr3 | 179342709 | 179399936 |
NA18965 | hp1 | a0001 | c0001 | t0002 | g0177 | EAS | JPT | MFN1_chr3_179342709_179399936 | MFN1 | chr3 | 179342709 | 179399936 |
NA18965 | hp2 | a0001 | c0001 | t0001 | g0226 | EAS | JPT | MFN1_chr3_179342709_179399936 | MFN1 | chr3 | 179342709 | 179399936 |
NA18967 | hp1 | a0001 | c0001 | t0003 | g0015 | EAS | JPT | MFN1_chr3_179342709_179399936 | MFN1 | chr3 | 179342709 | 179399936 |
NA18967 | hp2 | a0001 | c0001 | t0003 | g0262 | EAS | JPT | MFN1_chr3_179342709_179399936 | MFN1 | chr3 | 179342709 | 179399936 |
NA18968 | hp1 | a0001 | c0001 | t0011 | g0163 | EAS | JPT | MFN1_chr3_179342709_179399936 | MFN1 | chr3 | 179342709 | 179399936 |
NA18968 | hp2 | a0001 | c0001 | t0003 | g0122 | EAS | JPT | MFN1_chr3_179342709_179399936 | MFN1 | chr3 | 179342709 | 179399936 |
NA18970 | hp1 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | MFN1_chr3_179342709_179399936 | MFN1 | chr3 | 179342709 | 179399936 |
NA18970 | hp2 | a0001 | c0001 | t0008 | g0172 | EAS | JPT | MFN1_chr3_179342709_179399936 | MFN1 | chr3 | 179342709 | 179399936 |
NA18972 | hp1 | a0001 | c0001 | t0048 | g0128 | EAS | JPT | MFN1_chr3_179342709_179399936 | MFN1 | chr3 | 179342709 | 179399936 |
NA18972 | hp2 | a0001 | c0001 | t0001 | g0275 | EAS | JPT | MFN1_chr3_179342709_179399936 | MFN1 | chr3 | 179342709 | 179399936 |
NA18974 | hp1 | a0001 | c0001 | t0008 | g0189 | EAS | JPT | MFN1_chr3_179342709_179399936 | MFN1 | chr3 | 179342709 | 179399936 |
NA18974 | hp2 | a0001 | c0001 | t0002 | g0036 | EAS | JPT | MFN1_chr3_179342709_179399936 | MFN1 | chr3 | 179342709 | 179399936 |
NA18977 | hp1 | a0001 | c0001 | t0008 | g0197 | EAS | JPT | MFN1_chr3_179342709_179399936 | MFN1 | chr3 | 179342709 | 179399936 |
NA18977 | hp2 | a0001 | c0001 | t0001 | g0119 | EAS | JPT | MFN1_chr3_179342709_179399936 | MFN1 | chr3 | 179342709 | 179399936 |
NA18978 | hp1 | a0001 | c0001 | t0003 | g0110 | EAS | JPT | MFN1_chr3_179342709_179399936 | MFN1 | chr3 | 179342709 | 179399936 |
NA18978 | hp2 | a0001 | c0001 | t0008 | g0196 | EAS | JPT | MFN1_chr3_179342709_179399936 | MFN1 | chr3 | 179342709 | 179399936 |
NA18980 | hp1 | a0001 | c0001 | t0001 | g0041 | EAS | JPT | MFN1_chr3_179342709_179399936 | MFN1 | chr3 | 179342709 | 179399936 |
NA18980 | hp2 | a0001 | c0001 | t0001 | g0120 | EAS | JPT | MFN1_chr3_179342709_179399936 | MFN1 | chr3 | 179342709 | 179399936 |
NA18982 | hp1 | a0001 | c0001 | t0002 | g0202 | EAS | JPT | MFN1_chr3_179342709_179399936 | MFN1 | chr3 | 179342709 | 179399936 |
NA18982 | hp2 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | MFN1_chr3_179342709_179399936 | MFN1 | chr3 | 179342709 | 179399936 |
NA18983 | hp1 | a0001 | c0001 | t0001 | g0115 | EAS | JPT | MFN1_chr3_179342709_179399936 | MFN1 | chr3 | 179342709 | 179399936 |
NA18983 | hp2 | a0001 | c0001 | t0010 | g0081 | EAS | JPT | MFN1_chr3_179342709_179399936 | MFN1 | chr3 | 179342709 | 179399936 |
NA18984 | hp1 | a0001 | c0001 | t0002 | g0147 | EAS | JPT | MFN1_chr3_179342709_179399936 | MFN1 | chr3 | 179342709 | 179399936 |
NA18984 | hp2 | a0001 | c0001 | t0003 | g0002 | EAS | JPT | MFN1_chr3_179342709_179399936 | MFN1 | chr3 | 179342709 | 179399936 |
NA18985 | hp1 | a0001 | c0001 | t0001 | g0124 | EAS | JPT | MFN1_chr3_179342709_179399936 | MFN1 | chr3 | 179342709 | 179399936 |
NA18985 | hp2 | a0001 | c0001 | t0002 | g0169 | EAS | JPT | MFN1_chr3_179342709_179399936 | MFN1 | chr3 | 179342709 | 179399936 |
NA18986 | hp1 | a0001 | c0001 | t0007 | g0257 | EAS | JPT | MFN1_chr3_179342709_179399936 | MFN1 | chr3 | 179342709 | 179399936 |
NA18986 | hp2 | a0001 | c0004 | t0002 | g0174 | EAS | JPT | MFN1_chr3_179342709_179399936 | MFN1 | chr3 | 179342709 | 179399936 |
NA18988 | hp1 | a0001 | c0001 | t0002 | g0170 | EAS | JPT | MFN1_chr3_179342709_179399936 | MFN1 | chr3 | 179342709 | 179399936 |
NA18988 | hp2 | a0001 | c0001 | t0003 | g0268 | EAS | JPT | MFN1_chr3_179342709_179399936 | MFN1 | chr3 | 179342709 | 179399936 |
NA18990 | hp1 | a0001 | c0001 | t0001 | g0269 | EAS | JPT | MFN1_chr3_179342709_179399936 | MFN1 | chr3 | 179342709 | 179399936 |
NA18990 | hp2 | a0001 | c0001 | t0004 | g0026 | EAS | JPT | MFN1_chr3_179342709_179399936 | MFN1 | chr3 | 179342709 | 179399936 |
NA18991 | hp1 | a0001 | c0001 | t0003 | g0099 | EAS | JPT | MFN1_chr3_179342709_179399936 | MFN1 | chr3 | 179342709 | 179399936 |
NA18991 | hp2 | a0001 | c0001 | t0007 | g0259 | EAS | JPT | MFN1_chr3_179342709_179399936 | MFN1 | chr3 | 179342709 | 179399936 |
NA18993 | hp1 | a0001 | c0001 | t0001 | g0121 | EAS | JPT | MFN1_chr3_179342709_179399936 | MFN1 | chr3 | 179342709 | 179399936 |
NA18993 | hp2 | a0001 | c0001 | t0001 | g0270 | EAS | JPT | MFN1_chr3_179342709_179399936 | MFN1 | chr3 | 179342709 | 179399936 |
NA18994 | hp1 | a0001 | c0001 | t0047 | g0029 | EAS | JPT | MFN1_chr3_179342709_179399936 | MFN1 | chr3 | 179342709 | 179399936 |
NA18994 | hp2 | a0001 | c0001 | t0028 | g0188 | EAS | JPT | MFN1_chr3_179342709_179399936 | MFN1 | chr3 | 179342709 | 179399936 |
NA18995 | hp1 | a0001 | c0001 | t0007 | g0019 | EAS | JPT | MFN1_chr3_179342709_179399936 | MFN1 | chr3 | 179342709 | 179399936 |
NA18995 | hp2 | a0001 | c0004 | t0002 | g0198 | EAS | JPT | MFN1_chr3_179342709_179399936 | MFN1 | chr3 | 179342709 | 179399936 |
NA18998 | hp1 | a0001 | c0001 | t0002 | g0005 | EAS | JPT | MFN1_chr3_179342709_179399936 | MFN1 | chr3 | 179342709 | 179399936 |
NA18998 | hp2 | a0002 | c0003 | t0001 | g0235 | EAS | JPT | MFN1_chr3_179342709_179399936 | MFN1 | chr3 | 179342709 | 179399936 |
NA18999 | hp1 | a0001 | c0001 | t0001 | g0108 | EAS | JPT | MFN1_chr3_179342709_179399936 | MFN1 | chr3 | 179342709 | 179399936 |
NA18999 | hp2 | a0001 | c0001 | t0008 | g0037 | EAS | JPT | MFN1_chr3_179342709_179399936 | MFN1 | chr3 | 179342709 | 179399936 |
NA19003 | hp1 | a0001 | c0001 | t0002 | g0166 | EAS | JPT | MFN1_chr3_179342709_179399936 | MFN1 | chr3 | 179342709 | 179399936 |
NA19003 | hp2 | a0001 | c0001 | t0001 | g0044 | EAS | JPT | MFN1_chr3_179342709_179399936 | MFN1 | chr3 | 179342709 | 179399936 |
NA19005 | hp1 | a0001 | c0001 | t0010 | g0001 | EAS | JPT | MFN1_chr3_179342709_179399936 | MFN1 | chr3 | 179342709 | 179399936 |
NA19005 | hp2 | a0001 | c0001 | t0002 | g0005 | EAS | JPT | MFN1_chr3_179342709_179399936 | MFN1 | chr3 | 179342709 | 179399936 |
NA19011 | hp1 | a0001 | c0001 | t0002 | g0005 | EAS | JPT | MFN1_chr3_179342709_179399936 | MFN1 | chr3 | 179342709 | 179399936 |
NA19011 | hp2 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | MFN1_chr3_179342709_179399936 | MFN1 | chr3 | 179342709 | 179399936 |
NA19012 | hp1 | a0001 | c0001 | t0046 | g0087 | EAS | JPT | MFN1_chr3_179342709_179399936 | MFN1 | chr3 | 179342709 | 179399936 |
NA19012 | hp2 | a0001 | c0001 | t0001 | g0279 | EAS | JPT | MFN1_chr3_179342709_179399936 | MFN1 | chr3 | 179342709 | 179399936 |
NA19030 | hp1 | a0001 | c0001 | t0001 | g0004 | AFR | LWK | MFN1_chr3_179342709_179399936 | MFN1 | chr3 | 179342709 | 179399936 |
NA19030 | hp2 | a0001 | c0001 | t0019 | g0105 | AFR | LWK | MFN1_chr3_179342709_179399936 | MFN1 | chr3 | 179342709 | 179399936 |
NA19043 | hp1 | a0001 | c0005 | t0027 | g0288 | AFR | LWK | MFN1_chr3_179342709_179399936 | MFN1 | chr3 | 179342709 | 179399936 |
NA19043 | hp2 | a0001 | c0001 | t0012 | g0060 | AFR | LWK | MFN1_chr3_179342709_179399936 | MFN1 | chr3 | 179342709 | 179399936 |
NA19054 | hp1 | a0001 | c0001 | t0002 | g0036 | EAS | JPT | MFN1_chr3_179342709_179399936 | MFN1 | chr3 | 179342709 | 179399936 |
NA19054 | hp2 | a0001 | c0001 | t0029 | g0010 | EAS | JPT | MFN1_chr3_179342709_179399936 | MFN1 | chr3 | 179342709 | 179399936 |
NA19055 | hp1 | a0001 | c0001 | t0001 | g0255 | EAS | JPT | MFN1_chr3_179342709_179399936 | MFN1 | chr3 | 179342709 | 179399936 |
NA19055 | hp2 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | MFN1_chr3_179342709_179399936 | MFN1 | chr3 | 179342709 | 179399936 |
NA19056 | hp1 | a0001 | c0001 | t0002 | g0175 | EAS | JPT | MFN1_chr3_179342709_179399936 | MFN1 | chr3 | 179342709 | 179399936 |
NA19056 | hp2 | a0001 | c0001 | t0001 | g0034 | EAS | JPT | MFN1_chr3_179342709_179399936 | MFN1 | chr3 | 179342709 | 179399936 |
NA19057 | hp1 | a0001 | c0001 | t0001 | g0256 | EAS | JPT | MFN1_chr3_179342709_179399936 | MFN1 | chr3 | 179342709 | 179399936 |
NA19057 | hp2 | a0001 | c0001 | t0002 | g0164 | EAS | JPT | MFN1_chr3_179342709_179399936 | MFN1 | chr3 | 179342709 | 179399936 |
NA19058 | hp1 | a0001 | c0002 | t0004 | g0285 | EAS | JPT | MFN1_chr3_179342709_179399936 | MFN1 | chr3 | 179342709 | 179399936 |
NA19058 | hp2 | a0001 | c0001 | t0002 | g0157 | EAS | JPT | MFN1_chr3_179342709_179399936 | MFN1 | chr3 | 179342709 | 179399936 |
NA19059 | hp1 | a0001 | c0001 | t0002 | g0160 | EAS | JPT | MFN1_chr3_179342709_179399936 | MFN1 | chr3 | 179342709 | 179399936 |
NA19059 | hp2 | a0001 | c0001 | t0001 | g0241 | EAS | JPT | MFN1_chr3_179342709_179399936 | MFN1 | chr3 | 179342709 | 179399936 |
NA19060 | hp1 | a0001 | c0001 | t0001 | g0127 | EAS | JPT | MFN1_chr3_179342709_179399936 | MFN1 | chr3 | 179342709 | 179399936 |
NA19060 | hp2 | a0001 | c0001 | t0008 | g0209 | EAS | JPT | MFN1_chr3_179342709_179399936 | MFN1 | chr3 | 179342709 | 179399936 |
NA19065 | hp1 | a0001 | c0001 | t0001 | g0277 | EAS | JPT | MFN1_chr3_179342709_179399936 | MFN1 | chr3 | 179342709 | 179399936 |
NA19065 | hp2 | a0001 | c0001 | t0002 | g0005 | EAS | JPT | MFN1_chr3_179342709_179399936 | MFN1 | chr3 | 179342709 | 179399936 |
NA19066 | hp1 | a0001 | c0001 | t0001 | g0129 | EAS | JPT | MFN1_chr3_179342709_179399936 | MFN1 | chr3 | 179342709 | 179399936 |
NA19066 | hp2 | a0001 | c0001 | t0008 | g0171 | EAS | JPT | MFN1_chr3_179342709_179399936 | MFN1 | chr3 | 179342709 | 179399936 |
NA19068 | hp1 | a0001 | c0001 | t0001 | g0155 | EAS | JPT | MFN1_chr3_179342709_179399936 | MFN1 | chr3 | 179342709 | 179399936 |
NA19068 | hp2 | a0001 | c0001 | t0010 | g0027 | EAS | JPT | MFN1_chr3_179342709_179399936 | MFN1 | chr3 | 179342709 | 179399936 |
NA19070 | hp1 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | MFN1_chr3_179342709_179399936 | MFN1 | chr3 | 179342709 | 179399936 |
NA19070 | hp2 | a0001 | c0001 | t0001 | g0280 | EAS | JPT | MFN1_chr3_179342709_179399936 | MFN1 | chr3 | 179342709 | 179399936 |
NA19074 | hp1 | a0001 | c0001 | t0001 | g0044 | EAS | JPT | MFN1_chr3_179342709_179399936 | MFN1 | chr3 | 179342709 | 179399936 |
NA19074 | hp2 | a0001 | c0001 | t0001 | g0028 | EAS | JPT | MFN1_chr3_179342709_179399936 | MFN1 | chr3 | 179342709 | 179399936 |
NA19075 | hp1 | a0001 | c0001 | t0002 | g0165 | EAS | JPT | MFN1_chr3_179342709_179399936 | MFN1 | chr3 | 179342709 | 179399936 |
NA19075 | hp2 | a0001 | c0001 | t0001 | g0246 | EAS | JPT | MFN1_chr3_179342709_179399936 | MFN1 | chr3 | 179342709 | 179399936 |
NA19077 | hp1 | a0001 | c0001 | t0002 | g0193 | EAS | JPT | MFN1_chr3_179342709_179399936 | MFN1 | chr3 | 179342709 | 179399936 |
NA19077 | hp2 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | MFN1_chr3_179342709_179399936 | MFN1 | chr3 | 179342709 | 179399936 |
NA19078 | hp1 | a0001 | c0001 | t0007 | g0156 | EAS | JPT | MFN1_chr3_179342709_179399936 | MFN1 | chr3 | 179342709 | 179399936 |
NA19078 | hp2 | a0001 | c0001 | t0008 | g0017 | EAS | JPT | MFN1_chr3_179342709_179399936 | MFN1 | chr3 | 179342709 | 179399936 |
NA19081 | hp1 | a0001 | c0001 | t0007 | g0261 | EAS | JPT | MFN1_chr3_179342709_179399936 | MFN1 | chr3 | 179342709 | 179399936 |
NA19081 | hp2 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | MFN1_chr3_179342709_179399936 | MFN1 | chr3 | 179342709 | 179399936 |
NA19082 | hp1 | a0001 | c0001 | t0001 | g0028 | EAS | JPT | MFN1_chr3_179342709_179399936 | MFN1 | chr3 | 179342709 | 179399936 |
NA19082 | hp2 | a0001 | c0001 | t0002 | g0228 | EAS | JPT | MFN1_chr3_179342709_179399936 | MFN1 | chr3 | 179342709 | 179399936 |
NA19083 | hp1 | a0001 | c0001 | t0007 | g0263 | EAS | JPT | MFN1_chr3_179342709_179399936 | MFN1 | chr3 | 179342709 | 179399936 |
NA19083 | hp2 | a0001 | c0001 | t0008 | g0173 | EAS | JPT | MFN1_chr3_179342709_179399936 | MFN1 | chr3 | 179342709 | 179399936 |
NA19084 | hp1 | a0001 | c0001 | t0011 | g0154 | EAS | JPT | MFN1_chr3_179342709_179399936 | MFN1 | chr3 | 179342709 | 179399936 |
NA19084 | hp2 | a0001 | c0001 | t0010 | g0001 | EAS | JPT | MFN1_chr3_179342709_179399936 | MFN1 | chr3 | 179342709 | 179399936 |
NA19085 | hp1 | a0001 | c0001 | t0005 | g0003 | EAS | JPT | MFN1_chr3_179342709_179399936 | MFN1 | chr3 | 179342709 | 179399936 |
NA19085 | hp2 | a0001 | c0001 | t0001 | g0153 | EAS | JPT | MFN1_chr3_179342709_179399936 | MFN1 | chr3 | 179342709 | 179399936 |
NA19086 | hp1 | a0001 | c0001 | t0001 | g0015 | EAS | JPT | MFN1_chr3_179342709_179399936 | MFN1 | chr3 | 179342709 | 179399936 |
NA19086 | hp2 | a0001 | c0001 | t0002 | g0005 | EAS | JPT | MFN1_chr3_179342709_179399936 | MFN1 | chr3 | 179342709 | 179399936 |
NA19088 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | MFN1_chr3_179342709_179399936 | MFN1 | chr3 | 179342709 | 179399936 |
NA19088 | hp2 | a0001 | c0001 | t0001 | g0231 | EAS | JPT | MFN1_chr3_179342709_179399936 | MFN1 | chr3 | 179342709 | 179399936 |
NA19089 | hp1 | a0001 | c0001 | t0003 | g0240 | EAS | JPT | MFN1_chr3_179342709_179399936 | MFN1 | chr3 | 179342709 | 179399936 |
NA19089 | hp2 | a0001 | c0001 | t0004 | g0001 | EAS | JPT | MFN1_chr3_179342709_179399936 | MFN1 | chr3 | 179342709 | 179399936 |
NA19090 | hp1 | a0001 | c0001 | t0001 | g0234 | EAS | JPT | MFN1_chr3_179342709_179399936 | MFN1 | chr3 | 179342709 | 179399936 |
NA19090 | hp2 | a0001 | c0001 | t0005 | g0192 | EAS | JPT | MFN1_chr3_179342709_179399936 | MFN1 | chr3 | 179342709 | 179399936 |
NA19091 | hp1 | a0001 | c0001 | t0005 | g0179 | EAS | JPT | MFN1_chr3_179342709_179399936 | MFN1 | chr3 | 179342709 | 179399936 |
NA19091 | hp2 | a0001 | c0001 | t0001 | g0247 | EAS | JPT | MFN1_chr3_179342709_179399936 | MFN1 | chr3 | 179342709 | 179399936 |
NA19240 | hp1 | a0001 | c0001 | t0003 | g0271 | AFR | YRI | MFN1_chr3_179342709_179399936 | MFN1 | chr3 | 179342709 | 179399936 |
NA19240 | hp2 | a0001 | c0001 | t0009 | g0289 | AFR | YRI | MFN1_chr3_179342709_179399936 | MFN1 | chr3 | 179342709 | 179399936 |
NA20129 | hp1 | a0001 | c0001 | t0009 | g0058 | AFR | ASW | MFN1_chr3_179342709_179399936 | MFN1 | chr3 | 179342709 | 179399936 |
NA20129 | hp2 | a0001 | c0001 | t0001 | g0230 | AFR | ASW | MFN1_chr3_179342709_179399936 | MFN1 | chr3 | 179342709 | 179399936 |
NA20905 | hp1 | a0001 | c0001 | t0001 | g0016 | SAS | GIH | MFN1_chr3_179342709_179399936 | MFN1 | chr3 | 179342709 | 179399936 |
NA20905 | hp2 | a0001 | c0001 | t0004 | g0092 | SAS | GIH | MFN1_chr3_179342709_179399936 | MFN1 | chr3 | 179342709 | 179399936 |
HG02109 | hp1 | a0001 | c0001 | t0015 | g0302 | AFR | ACB | MFN1_chr3_179342709_179399936 | MFN1 | chr3 | 179342709 | 179399936 |
HG02109 | hp2 | a0001 | c0001 | t0006 | g0048 | AFR | ACB | MFN1_chr3_179342709_179399936 | MFN1 | chr3 | 179342709 | 179399936 |
HG02486 | hp1 | a0001 | c0001 | t0001 | g0249 | AFR | ACB | MFN1_chr3_179342709_179399936 | MFN1 | chr3 | 179342709 | 179399936 |
HG02486 | hp2 | a0001 | c0001 | t0006 | g0296 | AFR | ACB | MFN1_chr3_179342709_179399936 | MFN1 | chr3 | 179342709 | 179399936 |
HG02559 | hp1 | a0001 | c0001 | t0021 | g0009 | AFR | ACB | MFN1_chr3_179342709_179399936 | MFN1 | chr3 | 179342709 | 179399936 |
HG02559 | hp2 | a0001 | c0005 | t0027 | g0287 | AFR | ACB | MFN1_chr3_179342709_179399936 | MFN1 | chr3 | 179342709 | 179399936 |
HG03471 | hp1 | a0001 | c0001 | t0015 | g0301 | AFR | MSL | MFN1_chr3_179342709_179399936 | MFN1 | chr3 | 179342709 | 179399936 |
HG03471 | hp2 | a0001 | c0008 | t0019 | g0104 | AFR | MSL | MFN1_chr3_179342709_179399936 | MFN1 | chr3 | 179342709 | 179399936 |
HG06807 | hp1 | a0001 | c0001 | t0040 | g0021 | AFR | USA | MFN1_chr3_179342709_179399936 | MFN1 | chr3 | 179342709 | 179399936 |
HG06807 | hp2 | a0001 | c0001 | t0002 | g0182 | AFR | USA | MFN1_chr3_179342709_179399936 | MFN1 | chr3 | 179342709 | 179399936 |
NA20300 | hp1 | a0001 | c0001 | t0023 | g0303 | AFR | USA | MFN1_chr3_179342709_179399936 | MFN1 | chr3 | 179342709 | 179399936 |
NA20300 | hp2 | a0001 | c0001 | t0049 | g0042 | AFR | USA | MFN1_chr3_179342709_179399936 | MFN1 | chr3 | 179342709 | 179399936 |
NA21309 | hp1 | a0001 | c0001 | t0001 | g0139 | AFR | LWK | MFN1_chr3_179342709_179399936 | MFN1 | chr3 | 179342709 | 179399936 |
NA21309 | hp2 | a0001 | c0001 | t0003 | g0272 | AFR | LWK | MFN1_chr3_179342709_179399936 | MFN1 | chr3 | 179342709 | 179399936 |
homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0001 | g0012 | REF | REF | MFN1_chr3_179342709_179399936 | MFN1 | chr3 | 179342709 | 179399936 |
homoSapiens_grch38 | hp1 | a0001 | c0001 | t0001 | g0033 | REF | REF | MFN1_chr3_179342709_179399936 | MFN1 | chr3 | 179342709 | 179399936 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr3:179351927
|
G | A | 1 | a0002 | 2 | HG00597.hp1 NA18998.hp2 |
missense_variant | MODERATE | c.140G>A | p.Arg47Gln | MFN1 | ENSG00000171109.19 | transcript | ENST00000471841.6 | protein_coding | 3/18 | 249/5212 | 140/2226 | 47/741 | chr3 | 179351927 | ||
chr3:179351929
|
A | C | 1 | a0005 | 1 | HG03540.hp2 | missense_variant | MODERATE | c.142A>C | p.Ile48Leu | MFN1 | ENSG00000171109.19 | transcript | ENST00000471841.6 | protein_coding | 3/18 | 251/5212 | 142/2226 | 48/741 | chr3 | 179351929 | ||
chr3:179365149
|
G | A | 1 | a0003 | 1 | HG01978.hp1 | missense_variant | MODERATE | c.677G>A | p.Arg226Gln | MFN1 | ENSG00000171109.19 | transcript | ENST00000471841.6 | protein_coding | 7/18 | 786/5212 | 677/2226 | 226/741 | chr3 | 179365149 | ||
chr3:179390026
|
C | T | 1 | a0004 | 1 | HG03130.hp1 | missense_variant | MODERATE | c.2035C>T | p.Arg679Cys | MFN1 | ENSG00000171109.19 | transcript | ENST00000471841.6 | protein_coding | 17/18 | 2144/5212 | 2035/2226 | 679/741 | chr3 | 179390026 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr3:179358894
|
C | T | 1 | a0001c0005 | 2 | HG02559.hp2 NA19043.hp1 |
synonymous_variant | LOW | c.303C>T | p.Leu101Leu | MFN1 | ENSG00000171109.19 | transcript | ENST00000471841.6 | protein_coding | 4/18 | 412/5212 | 303/2226 | 101/741 | chr3 | 179358894 | ||
chr3:179362369
|
A | G | 1 | a0001c0009 | 1 | HG03453.hp1 | synonymous_variant | LOW | c.423A>G | p.Gln141Gln | MFN1 | ENSG00000171109.19 | transcript | ENST00000471841.6 | protein_coding | 5/18 | 532/5212 | 423/2226 | 141/741 | chr3 | 179362369 | ||
chr3:179367555
|
T | C | 2 | a0001c0002a0001c0005 | 8 | HG02559.hp2 HG03669.hp1 HG03688.hp2 others(5): Show |
synonymous_variant | LOW | c.870T>C | p.Ser290Ser | MFN1 | ENSG00000171109.19 | transcript | ENST00000471841.6 | protein_coding | 8/18 | 979/5212 | 870/2226 | 290/741 | chr3 | 179367555 | ||
chr3:179378397
|
C | T | 1 | a0001c0004 | 2 | NA18986.hp2 NA18995.hp2 |
synonymous_variant | LOW | c.1386C>T | p.Thr462Thr | MFN1 | ENSG00000171109.19 | transcript | ENST00000471841.6 | protein_coding | 13/18 | 1495/5212 | 1386/2226 | 462/741 | chr3 | 179378397 | ||
chr3:179378406
|
A | G | 1 | a0001c0008 | 1 | HG03471.hp2 | synonymous_variant | LOW | c.1395A>G | p.Val465Val | MFN1 | ENSG00000171109.19 | transcript | ENST00000471841.6 | protein_coding | 13/18 | 1504/5212 | 1395/2226 | 465/741 | chr3 | 179378406 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr3:179392175
|
G | C | 3 | a0001c0001t0019a0001c0001t0035a0001c0008t0019 | 5 | HG02647.hp1 HG02896.hp1 HG02965.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*116G>C | MFN1 | ENSG00000171109.19 | transcript | ENST00000471841.6 | protein_coding | 18/18 | 116 | chr3 | 179392175 | |||||
chr3:179392489
|
G | C | 1 | a0001c0001t0023 | 2 | HG02257.hp1 NA20300.hp1 |
3_prime_UTR_variant | MODIFIER | c.*430G>C | MFN1 | ENSG00000171109.19 | transcript | ENST00000471841.6 | protein_coding | 18/18 | 430 | chr3 | 179392489 | |||||
chr3:179392524
|
T | G | 2 | a0001c0001t0008a0001c0001t0024 | 14 | HG00408.hp2 HG01978.hp2 HG02080.hp2 others(11): Show |
3_prime_UTR_variant | MODIFIER | c.*465T>G | MFN1 | ENSG00000171109.19 | transcript | ENST00000471841.6 | protein_coding | 18/18 | 465 | chr3 | 179392524 | |||||
chr3:179392600
|
T | C | 1 | a0001c0001t0036 | 1 | HG02976.hp1 | 3_prime_UTR_variant | MODIFIER | c.*541T>C | MFN1 | ENSG00000171109.19 | transcript | ENST00000471841.6 | protein_coding | 18/18 | 541 | chr3 | 179392600 | |||||
chr3:179392605
|
G | A | 11 | a0001c0001t0006a0001c0001t0015a0001c0001t0020others(8): Show | 35 | HG01069.hp2 HG01071.hp1 HG01167.hp2 others(32): Show |
3_prime_UTR_variant | MODIFIER | c.*546G>A | MFN1 | ENSG00000171109.19 | transcript | ENST00000471841.6 | protein_coding | 18/18 | 546 | chr3 | 179392605 | |||||
chr3:179392781
|
T | A | 2 | a0001c0001t0041a0001c0001t0042 | 2 | HG02258.hp1 HG02809.hp1 |
3_prime_UTR_variant | MODIFIER | c.*722T>A | MFN1 | ENSG00000171109.19 | transcript | ENST00000471841.6 | protein_coding | 18/18 | 722 | chr3 | 179392781 | |||||
chr3:179392837
|
A | G | 2 | a0001c0001t0018a0001c0001t0034 | 7 | HG01069.hp1 HG01167.hp1 HG01884.hp1 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*778A>G | MFN1 | ENSG00000171109.19 | transcript | ENST00000471841.6 | protein_coding | 18/18 | 778 | chr3 | 179392837 | |||||
chr3:179392839
|
C | T | 1 | a0001c0001t0052 | 1 | HG03195.hp2 | 3_prime_UTR_variant | MODIFIER | c.*780C>T | MFN1 | ENSG00000171109.19 | transcript | ENST00000471841.6 | protein_coding | 18/18 | 780 | chr3 | 179392839 | |||||
chr3:179392839
|
CTGT | C | 2 | a0001c0001t0025a0001c0001t0037 | 3 | HG01069.hp2 HG01071.hp1 HG01175.hp1 |
3_prime_UTR_variant | MODIFIER | c.*785_*787delGTT | MFN1 | ENSG00000171109.19 | transcript | ENST00000471841.6 | protein_coding | 18/18 | 785 | INFO_REALIGN_3_PRIME | chr3 | 179392839 | ||||
chr3:179393272
|
T | C | 1 | a0001c0005t0027 | 2 | HG02559.hp2 NA19043.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1213T>C | MFN1 | ENSG00000171109.19 | transcript | ENST00000471841.6 | protein_coding | 18/18 | 1213 | chr3 | 179393272 | |||||
chr3:179393306
|
C | T | 1 | a0001c0001t0036 | 1 | HG02976.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1247C>T | MFN1 | ENSG00000171109.19 | transcript | ENST00000471841.6 | protein_coding | 18/18 | 1247 | chr3 | 179393306 | |||||
chr3:179393356
|
G | A | 9 | a0001c0001t0002a0001c0001t0005a0001c0001t0008others(6): Show | 92 | HG00140.hp2 HG00280.hp1 HG00408.hp2 others(89): Show |
3_prime_UTR_variant | MODIFIER | c.*1297G>A | MFN1 | ENSG00000171109.19 | transcript | ENST00000471841.6 | protein_coding | 18/18 | 1297 | chr3 | 179393356 | |||||
chr3:179393417
|
C | T | 5 | a0001c0001t0006a0001c0001t0021a0001c0001t0025others(2): Show | 21 | HG01069.hp2 HG01071.hp1 HG01175.hp1 others(18): Show |
3_prime_UTR_variant | MODIFIER | c.*1358C>T | MFN1 | ENSG00000171109.19 | transcript | ENST00000471841.6 | protein_coding | 18/18 | 1358 | chr3 | 179393417 | |||||
chr3:179393559
|
A | C | 1 | a0001c0001t0033 | 2 | HG02647.hp2 HG03225.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1500A>C | MFN1 | ENSG00000171109.19 | transcript | ENST00000471841.6 | protein_coding | 18/18 | 1500 | chr3 | 179393559 | |||||
chr3:179393561
|
A | G | 1 | a0001c0001t0044 | 1 | HG00609.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1502A>G | MFN1 | ENSG00000171109.19 | transcript | ENST00000471841.6 | protein_coding | 18/18 | 1502 | chr3 | 179393561 | |||||
chr3:179393702
|
C | A | 6 | a0001c0001t0009a0001c0001t0012a0001c0001t0018others(3): Show | 26 | HG00735.hp2 HG01069.hp1 HG01167.hp1 others(23): Show |
3_prime_UTR_variant | MODIFIER | c.*1643C>A | MFN1 | ENSG00000171109.19 | transcript | ENST00000471841.6 | protein_coding | 18/18 | 1643 | chr3 | 179393702 | |||||
chr3:179393750
|
T | C | 1 | a0001c0001t0046 | 1 | NA19012.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1691T>C | MFN1 | ENSG00000171109.19 | transcript | ENST00000471841.6 | protein_coding | 18/18 | 1691 | chr3 | 179393750 | |||||
chr3:179393760
|
A | G | 3 | a0001c0001t0015a0001c0001t0040a0001c0009t0039 | 8 | HG01167.hp2 HG01169.hp1 HG02109.hp1 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*1701A>G | MFN1 | ENSG00000171109.19 | transcript | ENST00000471841.6 | protein_coding | 18/18 | 1701 | chr3 | 179393760 | |||||
chr3:179393844
|
T | C | 3 | a0001c0001t0029a0001c0001t0047a0001c0001t0048 | 4 | NA18947.hp2 NA18972.hp1 NA18994.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*1785T>C | MFN1 | ENSG00000171109.19 | transcript | ENST00000471841.6 | protein_coding | 18/18 | 1785 | chr3 | 179393844 | |||||
chr3:179393888
|
A | G | 1 | a0001c0005t0027 | 2 | HG02559.hp2 NA19043.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1829A>G | MFN1 | ENSG00000171109.19 | transcript | ENST00000471841.6 | protein_coding | 18/18 | 1829 | chr3 | 179393888 | |||||
chr3:179393929
|
T | C | 2 | a0001c0001t0012a0004c0007t0012 | 7 | HG00735.hp2 HG01433.hp2 HG02055.hp2 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*1870T>C | MFN1 | ENSG00000171109.19 | transcript | ENST00000471841.6 | protein_coding | 18/18 | 1870 | chr3 | 179393929 | |||||
chr3:179394073
|
C | G | 6 | a0001c0001t0006a0001c0001t0021a0001c0001t0025others(3): Show | 22 | HG01069.hp2 HG01071.hp1 HG01175.hp1 others(19): Show |
3_prime_UTR_variant | MODIFIER | c.*2014C>G | MFN1 | ENSG00000171109.19 | transcript | ENST00000471841.6 | protein_coding | 18/18 | 2014 | chr3 | 179394073 | |||||
chr3:179394106
|
C | T | 3 | a0001c0001t0014a0001c0001t0022a0001c0001t0052 | 11 | HG00280.hp2 HG00323.hp2 HG01928.hp1 others(8): Show |
3_prime_UTR_variant | MODIFIER | c.*2047C>T | MFN1 | ENSG00000171109.19 | transcript | ENST00000471841.6 | protein_coding | 18/18 | 2047 | chr3 | 179394106 | |||||
chr3:179394113
|
G | T | 1 | a0001c0001t0051 | 1 | HG02630.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2054G>T | MFN1 | ENSG00000171109.19 | transcript | ENST00000471841.6 | protein_coding | 18/18 | 2054 | chr3 | 179394113 | |||||
chr3:179394408
|
C | CT | 19 | a0001c0001t0003a0001c0001t0004a0001c0001t0010others(16): Show | 79 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(76): Show |
3_prime_UTR_variant | MODIFIER | c.*2374dupT | MFN1 | ENSG00000171109.19 | transcript | ENST00000471841.6 | protein_coding | 18/18 | 2375 | INFO_REALIGN_3_PRIME | chr3 | 179394408 | ||||
chr3:179394408
|
C | CTT | 5 | a0001c0001t0017a0001c0001t0022a0001c0001t0031others(2): Show | 13 | HG00423.hp2 HG00735.hp1 HG01928.hp1 others(10): Show |
3_prime_UTR_variant | MODIFIER | c.*2373_*2374dupTT | MFN1 | ENSG00000171109.19 | transcript | ENST00000471841.6 | protein_coding | 18/18 | 2375 | INFO_REALIGN_3_PRIME | chr3 | 179394408 | ||||
chr3:179394408
|
C | CTTT | 3 | a0001c0001t0018a0001c0001t0032a0005c0010t0032 | 7 | HG01069.hp1 HG01167.hp1 HG01261.hp2 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*2372_*2374dupTTT | MFN1 | ENSG00000171109.19 | transcript | ENST00000471841.6 | protein_coding | 18/18 | 2375 | INFO_REALIGN_3_PRIME | chr3 | 179394408 | ||||
chr3:179394408
|
CT | C | 9 | a0001c0001t0002a0001c0001t0007a0001c0001t0008others(6): Show | 89 | HG00140.hp2 HG00423.hp1 HG00544.hp1 others(86): Show |
3_prime_UTR_variant | MODIFIER | c.*2374delT | MFN1 | ENSG00000171109.19 | transcript | ENST00000471841.6 | protein_coding | 18/18 | 2374 | INFO_REALIGN_3_PRIME | chr3 | 179394408 | ||||
chr3:179394408
|
CTTTTTTT others(3): Show |
C | 1 | a0001c0001t0049 | 1 | NA20300.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2365_*2374delTTTT others(6): Show |
MFN1 | ENSG00000171109.19 | transcript | ENST00000471841.6 | protein_coding | 18/18 | 2365 | INFO_REALIGN_3_PRIME | chr3 | 179394408 | ||||
chr3:179394427
|
TTTTTTTG others(1): Show |
T | 2 | a0001c0001t0009a0001c0001t0045 | 12 | HG02257.hp2 HG02572.hp2 HG02630.hp2 others(9): Show |
3_prime_UTR_variant | MODIFIER | c.*2369_*2376delTTTT others(4): Show |
MFN1 | ENSG00000171109.19 | transcript | ENST00000471841.6 | protein_coding | 18/18 | 2369 | chr3 | 179394427 | |||||
chr3:179394434
|
G | T | 4 | a0001c0001t0012a0001c0001t0018a0001c0001t0034others(1): Show | 14 | HG00735.hp2 HG01069.hp1 HG01167.hp1 others(11): Show |
3_prime_UTR_variant | MODIFIER | c.*2375G>T | MFN1 | ENSG00000171109.19 | transcript | ENST00000471841.6 | protein_coding | 18/18 | 2375 | chr3 | 179394434 | |||||
chr3:179394435
|
A | T | 4 | a0001c0001t0012a0001c0001t0018a0001c0001t0034others(1): Show | 14 | HG00735.hp2 HG01069.hp1 HG01167.hp1 others(11): Show |
3_prime_UTR_variant | MODIFIER | c.*2376A>T | MFN1 | ENSG00000171109.19 | transcript | ENST00000471841.6 | protein_coding | 18/18 | 2376 | chr3 | 179394435 | |||||
chr3:179394446
|
C | T | 11 | a0001c0001t0002a0001c0001t0005a0001c0001t0008others(8): Show | 101 | HG00140.hp2 HG00280.hp1 HG00408.hp2 others(98): Show |
3_prime_UTR_variant | MODIFIER | c.*2387C>T | MFN1 | ENSG00000171109.19 | transcript | ENST00000471841.6 | protein_coding | 18/18 | 2387 | chr3 | 179394446 | |||||
chr3:179394454
|
C | T | 1 | a0001c0001t0047 | 1 | NA18994.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2395C>T | MFN1 | ENSG00000171109.19 | transcript | ENST00000471841.6 | protein_coding | 18/18 | 2395 | chr3 | 179394454 | |||||
chr3:179394467
|
G | C | 2 | a0001c0001t0018a0001c0001t0034 | 7 | HG01069.hp1 HG01167.hp1 HG01884.hp1 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*2408G>C | MFN1 | ENSG00000171109.19 | transcript | ENST00000471841.6 | protein_coding | 18/18 | 2408 | chr3 | 179394467 | |||||
chr3:179394508
|
C | T | 9 | a0001c0001t0002a0001c0001t0005a0001c0001t0008others(6): Show | 92 | HG00140.hp2 HG00280.hp1 HG00408.hp2 others(89): Show |
3_prime_UTR_variant | MODIFIER | c.*2449C>T | MFN1 | ENSG00000171109.19 | transcript | ENST00000471841.6 | protein_coding | 18/18 | 2449 | chr3 | 179394508 | |||||
chr3:179394565
|
G | A | 15 | a0001c0001t0004a0001c0001t0010a0001c0001t0014others(12): Show | 58 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(55): Show |
3_prime_UTR_variant | MODIFIER | c.*2506G>A | MFN1 | ENSG00000171109.19 | transcript | ENST00000471841.6 | protein_coding | 18/18 | 2506 | chr3 | 179394565 | |||||
chr3:179394567
|
C | T | 11 | a0001c0001t0006a0001c0001t0015a0001c0001t0020others(8): Show | 35 | HG01069.hp2 HG01071.hp1 HG01167.hp2 others(32): Show |
3_prime_UTR_variant | MODIFIER | c.*2508C>T | MFN1 | ENSG00000171109.19 | transcript | ENST00000471841.6 | protein_coding | 18/18 | 2508 | chr3 | 179394567 | |||||
chr3:179394637
|
G | C | 2 | a0001c0001t0011a0001c0001t0028 | 9 | HG00280.hp1 HG00544.hp1 HG01257.hp2 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*2578G>C | MFN1 | ENSG00000171109.19 | transcript | ENST00000471841.6 | protein_coding | 18/18 | 2578 | chr3 | 179394637 | |||||
chr3:179394644
|
T | A | 1 | a0001c0009t0039 | 1 | HG03453.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2585T>A | MFN1 | ENSG00000171109.19 | transcript | ENST00000471841.6 | protein_coding | 18/18 | 2585 | chr3 | 179394644 | |||||
chr3:179394667
|
G | A | 1 | a0001c0001t0050 | 1 | HG00609.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2608G>A | MFN1 | ENSG00000171109.19 | transcript | ENST00000471841.6 | protein_coding | 18/18 | 2608 | chr3 | 179394667 | |||||
chr3:179394714
|
C | T | 1 | a0001c0001t0045 | 1 | HG03195.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2655C>T | MFN1 | ENSG00000171109.19 | transcript | ENST00000471841.6 | protein_coding | 18/18 | 2655 | chr3 | 179394714 | |||||
chr3:179394752
|
T | A | 1 | a0001c0001t0010 | 8 | HG00621.hp2 NA18946.hp1 NA18952.hp2 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*2693T>A | MFN1 | ENSG00000171109.19 | transcript | ENST00000471841.6 | protein_coding | 18/18 | 2693 | chr3 | 179394752 | |||||
chr3:179394877
|
A | T | 9 | a0001c0001t0002a0001c0001t0005a0001c0001t0008others(6): Show | 92 | HG00140.hp2 HG00280.hp1 HG00408.hp2 others(89): Show |
3_prime_UTR_variant | MODIFIER | c.*2818A>T | MFN1 | ENSG00000171109.19 | transcript | ENST00000471841.6 | protein_coding | 18/18 | 2818 | chr3 | 179394877 | |||||
chr3:179394907
|
G | A | 3 | a0001c0001t0019a0001c0001t0035a0001c0008t0019 | 5 | HG02647.hp1 HG02896.hp1 HG02965.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*2848G>A | MFN1 | ENSG00000171109.19 | transcript | ENST00000471841.6 | protein_coding | 18/18 | 2848 | chr3 | 179394907 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr3:179347883
|
G | T | 2 | a0001c0001t0023g0303a0001c0001t0023g0304 | 2 | HG02257.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.-8+73G>T | MFN1 | ENSG00000171109.19 | transcript | ENST00000471841.6 | protein_coding | 1/17 | chr3 | 179347883 | ||||||
chr3:179347943
|
G | A | 1 | a0001c0001t0001g0049 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.-8+133G>A | MFN1 | ENSG00000171109.19 | transcript | ENST00000471841.6 | protein_coding | 1/17 | chr3 | 179347943 | ||||||
chr3:179348039
|
C | T | 6 | a0001c0001t0015g0021a0001c0001t0015g0299a0001c0001t0015g0300others(3): Show | 7 | HG01167.hp2 HG01169.hp1 HG02109.hp1 others(4): Show |
intron_variant | MODIFIER | c.-8+229C>T | MFN1 | ENSG00000171109.19 | transcript | ENST00000471841.6 | protein_coding | 1/17 | chr3 | 179348039 | ||||||
chr3:179348126
|
G | A | 23 | a0001c0001t0009g0024a0001c0001t0009g0025a0001c0001t0009g0057others(20): Show | 25 | HG00735.hp2 HG01069.hp1 HG01167.hp1 others(22): Show |
intron_variant | MODIFIER | c.-8+316G>A | MFN1 | ENSG00000171109.19 | transcript | ENST00000471841.6 | protein_coding | 1/17 | chr3 | 179348126 | ||||||
chr3:179348232
|
G | A | 2 | a0001c0001t0001g0067a0001c0001t0001g0068 | 2 | HG01168.hp2 HG01169.hp2 |
intron_variant | MODIFIER | c.-8+422G>A | MFN1 | ENSG00000171109.19 | transcript | ENST00000471841.6 | protein_coding | 1/17 | chr3 | 179348232 | ||||||
chr3:179348313
|
T | C | 10 | a0001c0001t0004g0069a0001c0001t0014g0014a0001c0001t0014g0070others(7): Show | 11 | HG00280.hp2 HG00323.hp2 HG01515.hp2 others(8): Show |
intron_variant | MODIFIER | c.-8+503T>C | MFN1 | ENSG00000171109.19 | transcript | ENST00000471841.6 | protein_coding | 1/17 | chr3 | 179348313 | ||||||
chr3:179348329
|
T | A | 2 | a0001c0001t0001g0077a0001c0001t0001g0078 | 2 | HG01081.hp2 HG01106.hp1 |
intron_variant | MODIFIER | c.-7-516T>A | MFN1 | ENSG00000171109.19 | transcript | ENST00000471841.6 | protein_coding | 1/17 | chr3 | 179348329 | ||||||
chr3:179348494
|
C | G | 17 | a0001c0001t0006g0009a0001c0001t0006g0020a0001c0001t0006g0047others(14): Show | 22 | HG01069.hp2 HG01071.hp1 HG01175.hp1 others(19): Show |
intron_variant | MODIFIER | c.-7-351C>G | MFN1 | ENSG00000171109.19 | transcript | ENST00000471841.6 | protein_coding | 1/17 | chr3 | 179348494 | ||||||
chr3:179348516
|
T | C | 13 | a0001c0001t0004g0001a0001c0001t0004g0026a0001c0001t0004g0079others(10): Show | 23 | HG00140.hp1 HG00323.hp1 HG00438.hp1 others(20): Show |
intron_variant | MODIFIER | c.-7-329T>C | MFN1 | ENSG00000171109.19 | transcript | ENST00000471841.6 | protein_coding | 1/17 | chr3 | 179348516 | ||||||
chr3:179348588
|
C | A | 1 | a0001c0001t0007g0088 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.-7-257C>A | MFN1 | ENSG00000171109.19 | transcript | ENST00000471841.6 | protein_coding | 1/17 | chr3 | 179348588 | ||||||
chr3:179348666
|
T | C | 22 | a0001c0001t0004g0001a0001c0001t0004g0026a0001c0001t0004g0069others(19): Show | 32 | HG00140.hp1 HG00323.hp1 HG00438.hp1 others(29): Show |
intron_variant | MODIFIER | c.-7-179T>C | MFN1 | ENSG00000171109.19 | transcript | ENST00000471841.6 | protein_coding | 1/17 | chr3 | 179348666 | ||||||
chr3:179348668
|
A | G | 17 | a0001c0001t0009g0024a0001c0001t0009g0025a0001c0001t0009g0057others(14): Show | 18 | HG00735.hp2 HG01433.hp2 HG02257.hp2 others(15): Show |
intron_variant | MODIFIER | c.-7-177A>G | MFN1 | ENSG00000171109.19 | transcript | ENST00000471841.6 | protein_coding | 1/17 | chr3 | 179348668 | ||||||
chr3:179348995
|
C | T | 8 | a0001c0002t0004g0282a0001c0002t0004g0285a0001c0002t0016g0281others(5): Show | 8 | HG02559.hp2 HG03669.hp1 HG03688.hp2 others(5): Show |
intron_variant | MODIFIER | c.112+32C>T | MFN1 | ENSG00000171109.19 | transcript | ENST00000471841.6 | protein_coding | 2/17 | chr3 | 179348995 | ||||||
chr3:179349066
|
G | A | 24 | a0001c0001t0009g0024a0001c0001t0009g0025a0001c0001t0009g0057others(21): Show | 26 | HG00735.hp2 HG01069.hp1 HG01167.hp1 others(23): Show |
intron_variant | MODIFIER | c.112+103G>A | MFN1 | ENSG00000171109.19 | transcript | ENST00000471841.6 | protein_coding | 2/17 | chr3 | 179349066 | ||||||
chr3:179349449
|
G | T | 66 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0018others(63): Show | 82 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(79): Show |
intron_variant | MODIFIER | c.112+486G>T | MFN1 | ENSG00000171109.19 | transcript | ENST00000471841.6 | protein_coding | 2/17 | chr3 | 179349449 | ||||||
chr3:179349450
|
A | G | 8 | a0001c0002t0004g0282a0001c0002t0004g0285a0001c0002t0016g0281others(5): Show | 8 | HG02559.hp2 HG03669.hp1 HG03688.hp2 others(5): Show |
intron_variant | MODIFIER | c.112+487A>G | MFN1 | ENSG00000171109.19 | transcript | ENST00000471841.6 | protein_coding | 2/17 | chr3 | 179349450 | ||||||
chr3:179349475
|
G | T | 1 | a0001c0001t0023g0304 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.112+512G>T | MFN1 | ENSG00000171109.19 | transcript | ENST00000471841.6 | protein_coding | 2/17 | chr3 | 179349475 | ||||||
chr3:179349508
|
ACTT | A | 7 | a0001c0001t0001g0276a0001c0001t0001g0277a0001c0001t0001g0278others(4): Show | 7 | HG02257.hp1 NA18949.hp1 NA18961.hp1 others(4): Show |
intron_variant | MODIFIER | c.112+549_112+551del others(3): Show |
MFN1 | ENSG00000171109.19 | transcript | ENST00000471841.6 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr3 | 179349508 | |||||
chr3:179349512
|
C | CT | 58 | a0001c0001t0002g0228a0001c0001t0004g0001a0001c0001t0004g0069others(55): Show | 70 | HG00140.hp1 HG00280.hp2 HG00438.hp1 others(67): Show |
intron_variant | MODIFIER | c.112+563dupT | MFN1 | ENSG00000171109.19 | transcript | ENST00000471841.6 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr3 | 179349512 | |||||
chr3:179349581
|
T | A | 10 | a0001c0001t0014g0014a0001c0001t0014g0070a0001c0001t0014g0071others(7): Show | 11 | HG00280.hp2 HG00323.hp2 HG01928.hp1 others(8): Show |
intron_variant | MODIFIER | c.112+618T>A | MFN1 | ENSG00000171109.19 | transcript | ENST00000471841.6 | protein_coding | 2/17 | chr3 | 179349581 | ||||||
chr3:179349603
|
G | A | 1 | a0001c0001t0004g0026 | 2 | NA18612.hp1 NA18990.hp2 |
intron_variant | MODIFIER | c.112+640G>A | MFN1 | ENSG00000171109.19 | transcript | ENST00000471841.6 | protein_coding | 2/17 | chr3 | 179349603 | ||||||
chr3:179349729
|
C | T | 1 | a0001c0001t0001g0226 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.112+766C>T | MFN1 | ENSG00000171109.19 | transcript | ENST00000471841.6 | protein_coding | 2/17 | chr3 | 179349729 | ||||||
chr3:179349802
|
C | T | 1 | a0001c0009t0039g0225 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.112+839C>T | MFN1 | ENSG00000171109.19 | transcript | ENST00000471841.6 | protein_coding | 2/17 | chr3 | 179349802 | ||||||
chr3:179349985
|
G | C | 1 | a0001c0001t0005g0098 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.112+1022G>C | MFN1 | ENSG00000171109.19 | transcript | ENST00000471841.6 | protein_coding | 2/17 | chr3 | 179349985 | ||||||
chr3:179350151
|
CA | C | 35 | a0001c0001t0001g0217a0001c0001t0002g0038a0001c0001t0002g0218others(32): Show | 37 | HG00735.hp2 HG01069.hp1 HG01167.hp1 others(34): Show |
intron_variant | MODIFIER | c.112+1201delA | MFN1 | ENSG00000171109.19 | transcript | ENST00000471841.6 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr3 | 179350151 | |||||
chr3:179350181
|
A | G | 1 | a0001c0001t0001g0280 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.112+1218A>G | MFN1 | ENSG00000171109.19 | transcript | ENST00000471841.6 | protein_coding | 2/17 | chr3 | 179350181 | ||||||
chr3:179350258
|
A | G | 1 | a0001c0001t0001g0215 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.112+1295A>G | MFN1 | ENSG00000171109.19 | transcript | ENST00000471841.6 | protein_coding | 2/17 | chr3 | 179350258 | ||||||
chr3:179350456
|
A | T | 2 | a0001c0001t0009g0025a0001c0001t0009g0066 | 3 | HG02257.hp2 HG03139.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.113-1444A>T | MFN1 | ENSG00000171109.19 | transcript | ENST00000471841.6 | protein_coding | 2/17 | chr3 | 179350456 | ||||||
chr3:179350503
|
T | C | 1 | a0001c0001t0003g0099 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.113-1397T>C | MFN1 | ENSG00000171109.19 | transcript | ENST00000471841.6 | protein_coding | 2/17 | chr3 | 179350503 | ||||||
chr3:179350505
|
T | C | 53 | a0001c0001t0006g0009a0001c0001t0006g0020a0001c0001t0006g0047others(50): Show | 61 | HG00735.hp2 HG01069.hp1 HG01069.hp2 others(58): Show |
intron_variant | MODIFIER | c.113-1395T>C | MFN1 | ENSG00000171109.19 | transcript | ENST00000471841.6 | protein_coding | 2/17 | chr3 | 179350505 | ||||||
chr3:179350546
|
A | G | 1 | a0001c0001t0009g0065 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.113-1354A>G | MFN1 | ENSG00000171109.19 | transcript | ENST00000471841.6 | protein_coding | 2/17 | chr3 | 179350546 | ||||||
chr3:179350610
|
A | T | 66 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0018others(63): Show | 82 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(79): Show |
intron_variant | MODIFIER | c.113-1290A>T | MFN1 | ENSG00000171109.19 | transcript | ENST00000471841.6 | protein_coding | 2/17 | chr3 | 179350610 | ||||||
chr3:179350707
|
G | A | 1 | a0001c0009t0039g0225 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.113-1193G>A | MFN1 | ENSG00000171109.19 | transcript | ENST00000471841.6 | protein_coding | 2/17 | chr3 | 179350707 | ||||||
chr3:179350720
|
T | C | 1 | a0001c0001t0001g0230 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.113-1180T>C | MFN1 | ENSG00000171109.19 | transcript | ENST00000471841.6 | protein_coding | 2/17 | chr3 | 179350720 | ||||||
chr3:179350786
|
C | T | 1 | a0001c0001t0005g0098 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.113-1114C>T | MFN1 | ENSG00000171109.19 | transcript | ENST00000471841.6 | protein_coding | 2/17 | chr3 | 179350786 | ||||||
chr3:179350925
|
C | T | 6 | a0001c0001t0013g0013a0001c0001t0013g0212a0001c0001t0013g0213others(3): Show | 8 | HG01070.hp2 HG01257.hp1 HG01258.hp2 others(5): Show |
intron_variant | MODIFIER | c.113-975C>T | MFN1 | ENSG00000171109.19 | transcript | ENST00000471841.6 | protein_coding | 2/17 | chr3 | 179350925 | ||||||
chr3:179350944
|
C | T | 2 | a0001c0001t0004g0096a0001c0001t0017g0095 | 2 | HG01192.hp1 HG02602.hp2 |
intron_variant | MODIFIER | c.113-956C>T | MFN1 | ENSG00000171109.19 | transcript | ENST00000471841.6 | protein_coding | 2/17 | chr3 | 179350944 | ||||||
chr3:179350949
|
G | A | 17 | a0001c0001t0006g0009a0001c0001t0006g0020a0001c0001t0006g0047others(14): Show | 22 | HG01069.hp2 HG01071.hp1 HG01175.hp1 others(19): Show |
intron_variant | MODIFIER | c.113-951G>A | MFN1 | ENSG00000171109.19 | transcript | ENST00000471841.6 | protein_coding | 2/17 | chr3 | 179350949 | ||||||
chr3:179351166
|
T | A | 5 | a0001c0001t0019g0054a0001c0001t0019g0105a0001c0001t0019g0106others(2): Show | 5 | HG02647.hp1 HG02896.hp1 HG02965.hp1 others(2): Show |
intron_variant | MODIFIER | c.113-734T>A | MFN1 | ENSG00000171109.19 | transcript | ENST00000471841.6 | protein_coding | 2/17 | chr3 | 179351166 | ||||||
chr3:179351303
|
G | T | 1 | a0001c0001t0002g0211 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.113-597G>T | MFN1 | ENSG00000171109.19 | transcript | ENST00000471841.6 | protein_coding | 2/17 | chr3 | 179351303 | ||||||
chr3:179351722
|
T | C | 1 | a0001c0001t0018g0050 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.113-178T>C | MFN1 | ENSG00000171109.19 | transcript | ENST00000471841.6 | protein_coding | 2/17 | chr3 | 179351722 | ||||||
chr3:179351751
|
C | T | 1 | a0001c0001t0019g0106 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.113-149C>T | MFN1 | ENSG00000171109.19 | transcript | ENST00000471841.6 | protein_coding | 2/17 | chr3 | 179351751 | ||||||
chr3:179351805
|
A | G | 1 | a0001c0001t0036g0210 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.113-95A>G | MFN1 | ENSG00000171109.19 | transcript | ENST00000471841.6 | protein_coding | 2/17 | chr3 | 179351805 | ||||||
chr3:179352380
|
A | G | 67 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0018others(64): Show | 83 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(80): Show |
intron_variant | MODIFIER | c.248+345A>G | MFN1 | ENSG00000171109.19 | transcript | ENST00000471841.6 | protein_coding | 3/17 | chr3 | 179352380 | ||||||
chr3:179352433
|
A | C | 2 | a0001c0001t0014g0076a0001c0001t0022g0075 | 2 | HG03927.hp2 HG03942.hp2 |
intron_variant | MODIFIER | c.248+398A>C | MFN1 | ENSG00000171109.19 | transcript | ENST00000471841.6 | protein_coding | 3/17 | chr3 | 179352433 | ||||||
chr3:179352436
|
A | G | 2 | a0001c0001t0014g0076a0001c0001t0022g0075 | 2 | HG03927.hp2 HG03942.hp2 |
intron_variant | MODIFIER | c.248+401A>G | MFN1 | ENSG00000171109.19 | transcript | ENST00000471841.6 | protein_coding | 3/17 | chr3 | 179352436 | ||||||
chr3:179352437
|
C | A | 2 | a0001c0001t0014g0076a0001c0001t0022g0075 | 2 | HG03927.hp2 HG03942.hp2 |
intron_variant | MODIFIER | c.248+402C>A | MFN1 | ENSG00000171109.19 | transcript | ENST00000471841.6 | protein_coding | 3/17 | chr3 | 179352437 | ||||||
chr3:179352438
|
T | A | 2 | a0001c0001t0014g0076a0001c0001t0022g0075 | 2 | HG03927.hp2 HG03942.hp2 |
intron_variant | MODIFIER | c.248+403T>A | MFN1 | ENSG00000171109.19 | transcript | ENST00000471841.6 | protein_coding | 3/17 | chr3 | 179352438 | ||||||
chr3:179352440
|
T | G | 2 | a0001c0001t0014g0076a0001c0001t0022g0075 | 2 | HG03927.hp2 HG03942.hp2 |
intron_variant | MODIFIER | c.248+405T>G | MFN1 | ENSG00000171109.19 | transcript | ENST00000471841.6 | protein_coding | 3/17 | chr3 | 179352440 | ||||||
chr3:179352575
|
A | G | 1 | a0001c0001t0008g0209 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.248+540A>G | MFN1 | ENSG00000171109.19 | transcript | ENST00000471841.6 | protein_coding | 3/17 | chr3 | 179352575 | ||||||
chr3:179352595
|
G | A | 1 | a0001c0002t0016g0281 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.248+560G>A | MFN1 | ENSG00000171109.19 | transcript | ENST00000471841.6 | protein_coding | 3/17 | chr3 | 179352595 | ||||||
chr3:179352630
|
G | A | 1 | a0001c0009t0039g0225 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.248+595G>A | MFN1 | ENSG00000171109.19 | transcript | ENST00000471841.6 | protein_coding | 3/17 | chr3 | 179352630 | ||||||
chr3:179352666
|
C | T | 169 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0018others(166): Show | 205 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(202): Show |
intron_variant | MODIFIER | c.248+631C>T | MFN1 | ENSG00000171109.19 | transcript | ENST00000471841.6 | protein_coding | 3/17 | chr3 | 179352666 | ||||||
chr3:179352753
|
A | AT | 128 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0018others(125): Show | 152 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(149): Show |
intron_variant | MODIFIER | c.248+728dupT | MFN1 | ENSG00000171109.19 | transcript | ENST00000471841.6 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr3 | 179352753 | |||||
chr3:179352753
|
AT | A | 34 | a0001c0001t0004g0001a0001c0001t0004g0026a0001c0001t0004g0069others(31): Show | 46 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(43): Show |
intron_variant | MODIFIER | c.248+728delT | MFN1 | ENSG00000171109.19 | transcript | ENST00000471841.6 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr3 | 179352753 | |||||
chr3:179352796
|
C | T | 1 | a0001c0001t0052g0227 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.248+761C>T | MFN1 | ENSG00000171109.19 | transcript | ENST00000471841.6 | protein_coding | 3/17 | chr3 | 179352796 | ||||||
chr3:179352894
|
G | A | 6 | a0001c0002t0004g0282a0001c0002t0004g0285a0001c0002t0016g0281others(3): Show | 6 | HG03669.hp1 HG03688.hp2 HG03704.hp1 others(3): Show |
intron_variant | MODIFIER | c.248+859G>A | MFN1 | ENSG00000171109.19 | transcript | ENST00000471841.6 | protein_coding | 3/17 | chr3 | 179352894 | ||||||
chr3:179352998
|
C | T | 67 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0018others(64): Show | 83 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(80): Show |
intron_variant | MODIFIER | c.248+963C>T | MFN1 | ENSG00000171109.19 | transcript | ENST00000471841.6 | protein_coding | 3/17 | chr3 | 179352998 | ||||||
chr3:179353054
|
A | AT | 47 | a0001c0001t0001g0273a0001c0001t0001g0275a0001c0001t0003g0271others(44): Show | 54 | HG00735.hp2 HG01069.hp2 HG01071.hp1 others(51): Show |
intron_variant | MODIFIER | c.248+1019_248+1020i others(3): Show |
MFN1 | ENSG00000171109.19 | transcript | ENST00000471841.6 | protein_coding | 3/17 | chr3 | 179353054 | ||||||
chr3:179353055
|
A | AT | 77 | a0001c0001t0001g0155a0001c0001t0002g0003a0001c0001t0002g0005others(74): Show | 90 | HG00140.hp2 HG00280.hp1 HG00408.hp2 others(87): Show |
intron_variant | MODIFIER | c.248+1037dupT | MFN1 | ENSG00000171109.19 | transcript | ENST00000471841.6 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr3 | 179353055 | |||||
chr3:179353055
|
A | T | 168 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0018others(165): Show | 204 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(201): Show |
intron_variant | MODIFIER | c.248+1020A>T | MFN1 | ENSG00000171109.19 | transcript | ENST00000471841.6 | protein_coding | 3/17 | chr3 | 179353055 | ||||||
chr3:179353121
|
T | G | 2 | a0001c0001t0003g0271a0001c0001t0003g0272 | 2 | NA19240.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.248+1086T>G | MFN1 | ENSG00000171109.19 | transcript | ENST00000471841.6 | protein_coding | 3/17 | chr3 | 179353121 | ||||||
chr3:179353220
|
A | AT | 45 | a0001c0001t0001g0034a0001c0001t0001g0078a0001c0001t0001g0150others(42): Show | 58 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(55): Show |
intron_variant | MODIFIER | c.248+1203dupT | MFN1 | ENSG00000171109.19 | transcript | ENST00000471841.6 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr3 | 179353220 | |||||
chr3:179353220
|
A | ATT | 6 | a0001c0001t0015g0021a0001c0001t0015g0299a0001c0001t0015g0300others(3): Show | 7 | HG01167.hp2 HG01169.hp1 HG02109.hp1 others(4): Show |
intron_variant | MODIFIER | c.248+1202_248+1203d others(4): Show |
MFN1 | ENSG00000171109.19 | transcript | ENST00000471841.6 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr3 | 179353220 | |||||
chr3:179353220
|
AT | A | 63 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0018others(60): Show | 79 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(76): Show |
intron_variant | MODIFIER | c.248+1203delT | MFN1 | ENSG00000171109.19 | transcript | ENST00000471841.6 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr3 | 179353220 | |||||
chr3:179353409
|
T | C | 3 | a0001c0001t0009g0057a0001c0001t0009g0058a0001c0001t0009g0065 | 3 | HG02572.hp2 HG02630.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.248+1374T>C | MFN1 | ENSG00000171109.19 | transcript | ENST00000471841.6 | protein_coding | 3/17 | chr3 | 179353409 | ||||||
chr3:179353415
|
C | T | 1 | a0001c0001t0005g0098 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.248+1380C>T | MFN1 | ENSG00000171109.19 | transcript | ENST00000471841.6 | protein_coding | 3/17 | chr3 | 179353415 | ||||||
chr3:179353568
|
G | A | 1 | a0001c0001t0011g0154 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.248+1533G>A | MFN1 | ENSG00000171109.19 | transcript | ENST00000471841.6 | protein_coding | 3/17 | chr3 | 179353568 | ||||||
chr3:179353636
|
T | G | 2 | a0001c0001t0017g0039a0001c0001t0032g0229 | 3 | HG01261.hp2 HG02886.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.248+1601T>G | MFN1 | ENSG00000171109.19 | transcript | ENST00000471841.6 | protein_coding | 3/17 | chr3 | 179353636 | ||||||
chr3:179353726
|
G | C | 2 | a0001c0005t0027g0287a0001c0005t0027g0288 | 2 | HG02559.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.248+1691G>C | MFN1 | ENSG00000171109.19 | transcript | ENST00000471841.6 | protein_coding | 3/17 | chr3 | 179353726 | ||||||
chr3:179353752
|
C | T | 2 | a0001c0001t0002g0204a0001c0001t0005g0203 | 2 | HG01515.hp1 HG01517.hp1 |
intron_variant | MODIFIER | c.248+1717C>T | MFN1 | ENSG00000171109.19 | transcript | ENST00000471841.6 | protein_coding | 3/17 | chr3 | 179353752 | ||||||
chr3:179354053
|
G | C | 5 | a0001c0001t0020g0101a0001c0001t0020g0102a0001c0001t0020g0216others(2): Show | 5 | HG01433.hp1 HG02257.hp1 HG02280.hp1 others(2): Show |
intron_variant | MODIFIER | c.248+2018G>C | MFN1 | ENSG00000171109.19 | transcript | ENST00000471841.6 | protein_coding | 3/17 | chr3 | 179354053 | ||||||
chr3:179354159
|
G | A | 1 | a0001c0001t0001g0232 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.248+2124G>A | MFN1 | ENSG00000171109.19 | transcript | ENST00000471841.6 | protein_coding | 3/17 | chr3 | 179354159 | ||||||
chr3:179354166
|
C | T | 4 | a0001c0001t0015g0021a0001c0001t0015g0301a0001c0001t0015g0302others(1): Show | 5 | HG02109.hp1 HG02615.hp1 HG02809.hp2 others(2): Show |
intron_variant | MODIFIER | c.248+2131C>T | MFN1 | ENSG00000171109.19 | transcript | ENST00000471841.6 | protein_coding | 3/17 | chr3 | 179354166 | ||||||
chr3:179354440
|
A | C | 34 | a0001c0001t0004g0001a0001c0001t0004g0026a0001c0001t0004g0069others(31): Show | 46 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(43): Show |
intron_variant | MODIFIER | c.248+2405A>C | MFN1 | ENSG00000171109.19 | transcript | ENST00000471841.6 | protein_coding | 3/17 | chr3 | 179354440 | ||||||
chr3:179354555
|
G | A | 42 | a0001c0001t0001g0010a0001c0001t0001g0011a0001c0001t0001g0015others(39): Show | 51 | HG00438.hp2 HG00544.hp2 HG00597.hp2 others(48): Show |
intron_variant | MODIFIER | c.248+2520G>A | MFN1 | ENSG00000171109.19 | transcript | ENST00000471841.6 | protein_coding | 3/17 | chr3 | 179354555 | ||||||
chr3:179354556
|
G | C | 1 | a0001c0001t0001g0215 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.248+2521G>C | MFN1 | ENSG00000171109.19 | transcript | ENST00000471841.6 | protein_coding | 3/17 | chr3 | 179354556 | ||||||
chr3:179354568
|
T | C | 3 | a0001c0001t0006g0047a0001c0001t0026g0047a0001c0001t0026g0100 | 3 | HG02258.hp2 HG02615.hp2 HG02818.hp2 |
intron_variant | MODIFIER | c.248+2533T>C | MFN1 | ENSG00000171109.19 | transcript | ENST00000471841.6 | protein_coding | 3/17 | chr3 | 179354568 | ||||||
chr3:179354710
|
A | G | 8 | a0001c0002t0004g0282a0001c0002t0004g0285a0001c0002t0016g0281others(5): Show | 8 | HG02559.hp2 HG03669.hp1 HG03688.hp2 others(5): Show |
intron_variant | MODIFIER | c.248+2675A>G | MFN1 | ENSG00000171109.19 | transcript | ENST00000471841.6 | protein_coding | 3/17 | chr3 | 179354710 | ||||||
chr3:179354849
|
C | T | 1 | a0001c0001t0001g0267 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.248+2814C>T | MFN1 | ENSG00000171109.19 | transcript | ENST00000471841.6 | protein_coding | 3/17 | chr3 | 179354849 | ||||||
chr3:179354855
|
C | T | 1 | a0001c0001t0002g0202 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.248+2820C>T | MFN1 | ENSG00000171109.19 | transcript | ENST00000471841.6 | protein_coding | 3/17 | chr3 | 179354855 | ||||||
chr3:179354959
|
G | A | 1 | a0001c0001t0031g0132 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.248+2924G>A | MFN1 | ENSG00000171109.19 | transcript | ENST00000471841.6 | protein_coding | 3/17 | chr3 | 179354959 | ||||||
chr3:179355174
|
A | G | 8 | a0001c0002t0004g0282a0001c0002t0004g0285a0001c0002t0016g0281others(5): Show | 8 | HG02559.hp2 HG03669.hp1 HG03688.hp2 others(5): Show |
intron_variant | MODIFIER | c.248+3139A>G | MFN1 | ENSG00000171109.19 | transcript | ENST00000471841.6 | protein_coding | 3/17 | chr3 | 179355174 | ||||||
chr3:179355386
|
G | C | 2 | a0001c0001t0004g0091a0001c0001t0017g0090 | 2 | HG03225.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.248+3351G>C | MFN1 | ENSG00000171109.19 | transcript | ENST00000471841.6 | protein_coding | 3/17 | chr3 | 179355386 | ||||||
chr3:179355525
|
A | G | 6 | a0001c0001t0015g0021a0001c0001t0015g0299a0001c0001t0015g0300others(3): Show | 7 | HG01167.hp2 HG01169.hp1 HG02109.hp1 others(4): Show |
intron_variant | MODIFIER | c.249-3315A>G | MFN1 | ENSG00000171109.19 | transcript | ENST00000471841.6 | protein_coding | 3/17 | chr3 | 179355525 | ||||||
chr3:179355625
|
C | G | 2 | a0001c0001t0002g0204a0001c0001t0005g0203 | 2 | HG01515.hp1 HG01517.hp1 |
intron_variant | MODIFIER | c.249-3215C>G | MFN1 | ENSG00000171109.19 | transcript | ENST00000471841.6 | protein_coding | 3/17 | chr3 | 179355625 | ||||||
chr3:179355816
|
G | A | 4 | a0001c0001t0019g0054a0001c0001t0019g0106a0001c0001t0035g0103others(1): Show | 4 | HG02647.hp1 HG02896.hp1 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.249-3024G>A | MFN1 | ENSG00000171109.19 | transcript | ENST00000471841.6 | protein_coding | 3/17 | chr3 | 179355816 | ||||||
chr3:179355997
|
G | A | 4 | a0001c0001t0001g0040a0001c0001t0001g0041a0001c0001t0001g0234others(1): Show | 6 | HG00609.hp1 HG02056.hp1 HG02132.hp1 others(3): Show |
intron_variant | MODIFIER | c.249-2843G>A | MFN1 | ENSG00000171109.19 | transcript | ENST00000471841.6 | protein_coding | 3/17 | chr3 | 179355997 | ||||||
chr3:179356002
|
G | A | 1 | a0001c0001t0006g0290 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.249-2838G>A | MFN1 | ENSG00000171109.19 | transcript | ENST00000471841.6 | protein_coding | 3/17 | chr3 | 179356002 | ||||||
chr3:179356033
|
T | TTG | 34 | a0001c0001t0004g0001a0001c0001t0004g0026a0001c0001t0004g0069others(31): Show | 46 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(43): Show |
intron_variant | MODIFIER | c.249-2805_249-2804d others(4): Show |
MFN1 | ENSG00000171109.19 | transcript | ENST00000471841.6 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr3 | 179356033 | |||||
chr3:179356064
|
C | A | 2 | a0001c0001t0023g0303a0001c0001t0023g0304 | 2 | HG02257.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.249-2776C>A | MFN1 | ENSG00000171109.19 | transcript | ENST00000471841.6 | protein_coding | 3/17 | chr3 | 179356064 | ||||||
chr3:179356120
|
A | G | 1 | a0001c0001t0001g0153 | 1 | NA19085.hp2 | intron_variant | MODIFIER | c.249-2720A>G | MFN1 | ENSG00000171109.19 | transcript | ENST00000471841.6 | protein_coding | 3/17 | chr3 | 179356120 | ||||||
chr3:179356385
|
G | A | 40 | a0001c0001t0004g0001a0001c0001t0004g0026a0001c0001t0004g0069others(37): Show | 52 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(49): Show |
intron_variant | MODIFIER | c.249-2455G>A | MFN1 | ENSG00000171109.19 | transcript | ENST00000471841.6 | protein_coding | 3/17 | chr3 | 179356385 | ||||||
chr3:179356480
|
A | G | 6 | a0001c0001t0006g0047a0001c0001t0006g0296a0001c0001t0006g0297others(3): Show | 6 | HG02258.hp2 HG02486.hp2 HG02615.hp2 others(3): Show |
intron_variant | MODIFIER | c.249-2360A>G | MFN1 | ENSG00000171109.19 | transcript | ENST00000471841.6 | protein_coding | 3/17 | chr3 | 179356480 | ||||||
chr3:179356630
|
C | T | 39 | a0001c0001t0004g0001a0001c0001t0004g0026a0001c0001t0004g0069others(36): Show | 51 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(48): Show |
intron_variant | MODIFIER | c.249-2210C>T | MFN1 | ENSG00000171109.19 | transcript | ENST00000471841.6 | protein_coding | 3/17 | chr3 | 179356630 | ||||||
chr3:179356749
|
A | G | 5 | a0001c0001t0019g0054a0001c0001t0019g0105a0001c0001t0019g0106others(2): Show | 5 | HG02647.hp1 HG02896.hp1 HG02965.hp1 others(2): Show |
intron_variant | MODIFIER | c.249-2091A>G | MFN1 | ENSG00000171109.19 | transcript | ENST00000471841.6 | protein_coding | 3/17 | chr3 | 179356749 | ||||||
chr3:179356780
|
C | A | 2 | a0002c0003t0001g0235a0002c0003t0003g0236 | 2 | HG00597.hp1 NA18998.hp2 |
intron_variant | MODIFIER | c.249-2060C>A | MFN1 | ENSG00000171109.19 | transcript | ENST00000471841.6 | protein_coding | 3/17 | chr3 | 179356780 | ||||||
chr3:179356827
|
G | T | 169 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0018others(166): Show | 205 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(202): Show |
intron_variant | MODIFIER | c.249-2013G>T | MFN1 | ENSG00000171109.19 | transcript | ENST00000471841.6 | protein_coding | 3/17 | chr3 | 179356827 | ||||||
chr3:179356908
|
C | T | 5 | a0001c0001t0020g0101a0001c0001t0020g0102a0001c0001t0020g0216others(2): Show | 5 | HG01433.hp1 HG02257.hp1 HG02280.hp1 others(2): Show |
intron_variant | MODIFIER | c.249-1932C>T | MFN1 | ENSG00000171109.19 | transcript | ENST00000471841.6 | protein_coding | 3/17 | chr3 | 179356908 | ||||||
chr3:179356924
|
G | C | 17 | a0001c0001t0006g0009a0001c0001t0006g0020a0001c0001t0006g0047others(14): Show | 22 | HG01069.hp2 HG01071.hp1 HG01175.hp1 others(19): Show |
intron_variant | MODIFIER | c.249-1916G>C | MFN1 | ENSG00000171109.19 | transcript | ENST00000471841.6 | protein_coding | 3/17 | chr3 | 179356924 | ||||||
chr3:179356988
|
A | G | 2 | a0001c0001t0012g0056a0001c0001t0012g0097 | 2 | HG02055.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.249-1852A>G | MFN1 | ENSG00000171109.19 | transcript | ENST00000471841.6 | protein_coding | 3/17 | chr3 | 179356988 | ||||||
chr3:179357089
|
A | G | 6 | a0001c0001t0006g0047a0001c0001t0006g0296a0001c0001t0006g0297others(3): Show | 6 | HG02258.hp2 HG02486.hp2 HG02615.hp2 others(3): Show |
intron_variant | MODIFIER | c.249-1751A>G | MFN1 | ENSG00000171109.19 | transcript | ENST00000471841.6 | protein_coding | 3/17 | chr3 | 179357089 | ||||||
chr3:179357095
|
C | T | 67 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0018others(64): Show | 83 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(80): Show |
intron_variant | MODIFIER | c.249-1745C>T | MFN1 | ENSG00000171109.19 | transcript | ENST00000471841.6 | protein_coding | 3/17 | chr3 | 179357095 | ||||||
chr3:179357169
|
C | T | 1 | a0001c0009t0039g0225 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.249-1671C>T | MFN1 | ENSG00000171109.19 | transcript | ENST00000471841.6 | protein_coding | 3/17 | chr3 | 179357169 | ||||||
chr3:179357272
|
A | C | 66 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0018others(63): Show | 82 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(79): Show |
intron_variant | MODIFIER | c.249-1568A>C | MFN1 | ENSG00000171109.19 | transcript | ENST00000471841.6 | protein_coding | 3/17 | chr3 | 179357272 | ||||||
chr3:179357294
|
A | G | 78 | a0001c0001t0002g0003a0001c0001t0002g0005a0001c0001t0002g0006others(75): Show | 91 | HG00140.hp2 HG00280.hp1 HG00408.hp2 others(88): Show |
intron_variant | MODIFIER | c.249-1546A>G | MFN1 | ENSG00000171109.19 | transcript | ENST00000471841.6 | protein_coding | 3/17 | chr3 | 179357294 | ||||||
chr3:179357305
|
T | C | 1 | a0001c0001t0035g0103 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.249-1535T>C | MFN1 | ENSG00000171109.19 | transcript | ENST00000471841.6 | protein_coding | 3/17 | chr3 | 179357305 | ||||||
chr3:179357306
|
G | T | 6 | a0001c0002t0004g0282a0001c0002t0004g0285a0001c0002t0016g0281others(3): Show | 6 | HG03669.hp1 HG03688.hp2 HG03704.hp1 others(3): Show |
intron_variant | MODIFIER | c.249-1534G>T | MFN1 | ENSG00000171109.19 | transcript | ENST00000471841.6 | protein_coding | 3/17 | chr3 | 179357306 | ||||||
chr3:179357341
|
T | C | 4 | a0001c0001t0019g0054a0001c0001t0019g0106a0001c0001t0035g0103others(1): Show | 4 | HG02647.hp1 HG02896.hp1 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.249-1499T>C | MFN1 | ENSG00000171109.19 | transcript | ENST00000471841.6 | protein_coding | 3/17 | chr3 | 179357341 | ||||||
chr3:179357454
|
A | G | 1 | a0001c0001t0009g0063 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.249-1386A>G | MFN1 | ENSG00000171109.19 | transcript | ENST00000471841.6 | protein_coding | 3/17 | chr3 | 179357454 | ||||||
chr3:179357675
|
G | A | 247 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0018others(244): Show | 296 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(293): Show |
intron_variant | MODIFIER | c.249-1165G>A | MFN1 | ENSG00000171109.19 | transcript | ENST00000471841.6 | protein_coding | 3/17 | chr3 | 179357675 | ||||||
chr3:179357706
|
G | A | 1 | a0001c0009t0039g0225 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.249-1134G>A | MFN1 | ENSG00000171109.19 | transcript | ENST00000471841.6 | protein_coding | 3/17 | chr3 | 179357706 | ||||||
chr3:179357947
|
T | A | 5 | a0001c0001t0019g0054a0001c0001t0019g0105a0001c0001t0019g0106others(2): Show | 5 | HG02647.hp1 HG02896.hp1 HG02965.hp1 others(2): Show |
intron_variant | MODIFIER | c.249-893T>A | MFN1 | ENSG00000171109.19 | transcript | ENST00000471841.6 | protein_coding | 3/17 | chr3 | 179357947 | ||||||
chr3:179357950
|
T | G | 3 | a0001c0001t0020g0101a0001c0001t0020g0102a0001c0001t0020g0216 | 3 | HG01433.hp1 HG02280.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.249-890T>G | MFN1 | ENSG00000171109.19 | transcript | ENST00000471841.6 | protein_coding | 3/17 | chr3 | 179357950 | ||||||
chr3:179358150
|
G | GT | 170 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0016others(167): Show | 210 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(207): Show |
intron_variant | MODIFIER | c.249-672dupT | MFN1 | ENSG00000171109.19 | transcript | ENST00000471841.6 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr3 | 179358150 | |||||
chr3:179358150
|
G | GTT | 45 | a0001c0001t0001g0041a0001c0001t0001g0266a0001c0001t0001g0275others(42): Show | 54 | HG00408.hp2 HG01069.hp1 HG01069.hp2 others(51): Show |
intron_variant | MODIFIER | c.249-673_249-672dup others(2): Show |
MFN1 | ENSG00000171109.19 | transcript | ENST00000471841.6 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr3 | 179358150 | |||||
chr3:179358150
|
G | GTTT | 10 | a0001c0001t0006g0295a0001c0001t0009g0063a0001c0001t0012g0023others(7): Show | 10 | HG01433.hp2 HG02055.hp2 HG02257.hp1 others(7): Show |
intron_variant | MODIFIER | c.249-674_249-672dup others(3): Show |
MFN1 | ENSG00000171109.19 | transcript | ENST00000471841.6 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr3 | 179358150 | |||||
chr3:179358150
|
G | GTTTT | 11 | a0001c0001t0009g0024a0001c0001t0009g0025a0001c0001t0009g0057others(8): Show | 12 | HG00735.hp2 HG02257.hp2 HG02572.hp2 others(9): Show |
intron_variant | MODIFIER | c.249-675_249-672dup others(4): Show |
MFN1 | ENSG00000171109.19 | transcript | ENST00000471841.6 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr3 | 179358150 | |||||
chr3:179358156
|
T | TTTG | 6 | a0001c0001t0015g0021a0001c0001t0015g0299a0001c0001t0015g0300others(3): Show | 7 | HG01167.hp2 HG01169.hp1 HG02109.hp1 others(4): Show |
intron_variant | MODIFIER | c.249-682_249-681ins others(3): Show |
MFN1 | ENSG00000171109.19 | transcript | ENST00000471841.6 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr3 | 179358156 | |||||
chr3:179358158
|
T | TG | 7 | a0001c0001t0001g0042a0001c0001t0001g0237a0001c0001t0001g0238others(4): Show | 7 | HG00408.hp1 HG00597.hp1 HG01106.hp2 others(4): Show |
intron_variant | MODIFIER | c.249-682_249-681ins others(1): Show |
MFN1 | ENSG00000171109.19 | transcript | ENST00000471841.6 | protein_coding | 3/17 | chr3 | 179358158 | ||||||
chr3:179358254
|
G | A | 5 | a0001c0001t0020g0101a0001c0001t0020g0102a0001c0001t0020g0216others(2): Show | 5 | HG01433.hp1 HG02257.hp1 HG02280.hp1 others(2): Show |
intron_variant | MODIFIER | c.249-586G>A | MFN1 | ENSG00000171109.19 | transcript | ENST00000471841.6 | protein_coding | 3/17 | chr3 | 179358254 | ||||||
chr3:179358310
|
C | T | 1 | a0001c0001t0002g0036 | 2 | NA18974.hp2 NA19054.hp1 |
intron_variant | MODIFIER | c.249-530C>T | MFN1 | ENSG00000171109.19 | transcript | ENST00000471841.6 | protein_coding | 3/17 | chr3 | 179358310 | ||||||
chr3:179358424
|
A | G | 1 | a0001c0001t0048g0128 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.249-416A>G | MFN1 | ENSG00000171109.19 | transcript | ENST00000471841.6 | protein_coding | 3/17 | chr3 | 179358424 | ||||||
chr3:179358433
|
G | A | 2 | a0001c0005t0027g0287a0001c0005t0027g0288 | 2 | HG02559.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.249-407G>A | MFN1 | ENSG00000171109.19 | transcript | ENST00000471841.6 | protein_coding | 3/17 | chr3 | 179358433 | ||||||
chr3:179358440
|
A | G | 1 | a0001c0009t0039g0225 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.249-400A>G | MFN1 | ENSG00000171109.19 | transcript | ENST00000471841.6 | protein_coding | 3/17 | chr3 | 179358440 | ||||||
chr3:179358609
|
G | A | 2 | a0001c0001t0002g0158a0001c0001t0002g0159 | 2 | HG00738.hp1 HG01243.hp2 |
intron_variant | MODIFIER | c.249-231G>A | MFN1 | ENSG00000171109.19 | transcript | ENST00000471841.6 | protein_coding | 3/17 | chr3 | 179358609 | ||||||
chr3:179358616
|
A | G | 18 | a0001c0001t0009g0024a0001c0001t0009g0025a0001c0001t0009g0057others(15): Show | 19 | HG00735.hp2 HG01433.hp2 HG02055.hp2 others(16): Show |
intron_variant | MODIFIER | c.249-224A>G | MFN1 | ENSG00000171109.19 | transcript | ENST00000471841.6 | protein_coding | 3/17 | chr3 | 179358616 | ||||||
chr3:179359060
|
C | G | 3 | a0001c0001t0001g0046a0001c0001t0001g0264a0001c0001t0007g0274 | 4 | HG03239.hp1 HG03490.hp2 HG03492.hp1 others(1): Show |
intron_variant | MODIFIER | c.411+58C>G | MFN1 | ENSG00000171109.19 | transcript | ENST00000471841.6 | protein_coding | 4/17 | chr3 | 179359060 | ||||||
chr3:179359091
|
C | T | 53 | a0001c0001t0006g0009a0001c0001t0006g0020a0001c0001t0006g0047others(50): Show | 61 | HG00735.hp2 HG01069.hp1 HG01069.hp2 others(58): Show |
intron_variant | MODIFIER | c.411+89C>T | MFN1 | ENSG00000171109.19 | transcript | ENST00000471841.6 | protein_coding | 4/17 | chr3 | 179359091 | ||||||
chr3:179359127
|
CT | C | 66 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0018others(63): Show | 82 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(79): Show |
intron_variant | MODIFIER | c.411+136delT | MFN1 | ENSG00000171109.19 | transcript | ENST00000471841.6 | protein_coding | 4/17 | INFO_REALIGN_3_PRIME | chr3 | 179359127 | |||||
chr3:179359159
|
C | T | 34 | a0001c0001t0004g0001a0001c0001t0004g0026a0001c0001t0004g0069others(31): Show | 46 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(43): Show |
intron_variant | MODIFIER | c.411+157C>T | MFN1 | ENSG00000171109.19 | transcript | ENST00000471841.6 | protein_coding | 4/17 | chr3 | 179359159 | ||||||
chr3:179359264
|
G | A | 6 | a0001c0001t0015g0021a0001c0001t0015g0299a0001c0001t0015g0300others(3): Show | 7 | HG01167.hp2 HG01169.hp1 HG02109.hp1 others(4): Show |
intron_variant | MODIFIER | c.411+262G>A | MFN1 | ENSG00000171109.19 | transcript | ENST00000471841.6 | protein_coding | 4/17 | chr3 | 179359264 | ||||||
chr3:179359302
|
G | A | 34 | a0001c0001t0004g0001a0001c0001t0004g0026a0001c0001t0004g0069others(31): Show | 46 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(43): Show |
intron_variant | MODIFIER | c.411+300G>A | MFN1 | ENSG00000171109.19 | transcript | ENST00000471841.6 | protein_coding | 4/17 | chr3 | 179359302 | ||||||
chr3:179359419
|
C | CT | 45 | a0001c0001t0001g0131a0001c0001t0001g0226a0001c0001t0001g0234others(42): Show | 47 | HG01069.hp1 HG01167.hp1 HG01167.hp2 others(44): Show |
intron_variant | MODIFIER | c.411+436dupT | MFN1 | ENSG00000171109.19 | transcript | ENST00000471841.6 | protein_coding | 4/17 | INFO_REALIGN_3_PRIME | chr3 | 179359419 | |||||
chr3:179359567
|
C | T | 40 | a0001c0001t0004g0001a0001c0001t0004g0026a0001c0001t0004g0069others(37): Show | 52 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(49): Show |
intron_variant | MODIFIER | c.411+565C>T | MFN1 | ENSG00000171109.19 | transcript | ENST00000471841.6 | protein_coding | 4/17 | chr3 | 179359567 | ||||||
chr3:179359593
|
G | A | 1 | a0001c0001t0002g0194 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.411+591G>A | MFN1 | ENSG00000171109.19 | transcript | ENST00000471841.6 | protein_coding | 4/17 | chr3 | 179359593 | ||||||
chr3:179359596
|
C | CT | 80 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0018others(77): Show | 97 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(94): Show |
intron_variant | MODIFIER | c.411+617dupT | MFN1 | ENSG00000171109.19 | transcript | ENST00000471841.6 | protein_coding | 4/17 | INFO_REALIGN_3_PRIME | chr3 | 179359596 | |||||
chr3:179359596
|
C | CTT | 59 | a0001c0001t0001g0232a0001c0001t0001g0266a0001c0001t0001g0276others(56): Show | 72 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(69): Show |
intron_variant | MODIFIER | c.411+616_411+617dup others(2): Show |
MFN1 | ENSG00000171109.19 | transcript | ENST00000471841.6 | protein_coding | 4/17 | INFO_REALIGN_3_PRIME | chr3 | 179359596 | |||||
chr3:179359596
|
CT | C | 13 | a0001c0001t0001g0015a0001c0001t0001g0067a0001c0001t0001g0077others(10): Show | 14 | HG01081.hp1 HG01081.hp2 HG01106.hp1 others(11): Show |
intron_variant | MODIFIER | c.411+617delT | MFN1 | ENSG00000171109.19 | transcript | ENST00000471841.6 | protein_coding | 4/17 | INFO_REALIGN_3_PRIME | chr3 | 179359596 | |||||
chr3:179359596
|
CTTTTTT | C | 18 | a0001c0001t0006g0009a0001c0001t0006g0020a0001c0001t0006g0047others(15): Show | 23 | HG01069.hp2 HG01071.hp1 HG01175.hp1 others(20): Show |
intron_variant | MODIFIER | c.411+612_411+617del others(6): Show |
MFN1 | ENSG00000171109.19 | transcript | ENST00000471841.6 | protein_coding | 4/17 | INFO_REALIGN_3_PRIME | chr3 | 179359596 | |||||
chr3:179359596
|
CTTTTTTT others(3): Show |
C | 1 | a0001c0001t0005g0098 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.411+608_411+617del others(10): Show |
MFN1 | ENSG00000171109.19 | transcript | ENST00000471841.6 | protein_coding | 4/17 | INFO_REALIGN_3_PRIME | chr3 | 179359596 | |||||
chr3:179359674
|
A | G | 1 | a0001c0001t0001g0145 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.411+672A>G | MFN1 | ENSG00000171109.19 | transcript | ENST00000471841.6 | protein_coding | 4/17 | chr3 | 179359674 | ||||||
chr3:179359724
|
G | A | 5 | a0001c0001t0019g0054a0001c0001t0019g0105a0001c0001t0019g0106others(2): Show | 5 | HG02647.hp1 HG02896.hp1 HG02965.hp1 others(2): Show |
intron_variant | MODIFIER | c.411+722G>A | MFN1 | ENSG00000171109.19 | transcript | ENST00000471841.6 | protein_coding | 4/17 | chr3 | 179359724 | ||||||
chr3:179359829
|
G | A | 1 | a0001c0001t0005g0098 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.411+827G>A | MFN1 | ENSG00000171109.19 | transcript | ENST00000471841.6 | protein_coding | 4/17 | chr3 | 179359829 | ||||||
chr3:179359831
|
G | GA | 5 | a0001c0001t0020g0101a0001c0001t0020g0102a0001c0001t0020g0216others(2): Show | 5 | HG01433.hp1 HG02257.hp1 HG02280.hp1 others(2): Show |
intron_variant | MODIFIER | c.411+835dupA | MFN1 | ENSG00000171109.19 | transcript | ENST00000471841.6 | protein_coding | 4/17 | INFO_REALIGN_3_PRIME | chr3 | 179359831 | |||||
chr3:179359863
|
A | G | 24 | a0001c0001t0009g0024a0001c0001t0009g0025a0001c0001t0009g0057others(21): Show | 26 | HG00735.hp2 HG01069.hp1 HG01167.hp1 others(23): Show |
intron_variant | MODIFIER | c.411+861A>G | MFN1 | ENSG00000171109.19 | transcript | ENST00000471841.6 | protein_coding | 4/17 | chr3 | 179359863 | ||||||
chr3:179359892
|
A | G | 4 | a0001c0001t0019g0054a0001c0001t0019g0106a0001c0001t0035g0103others(1): Show | 4 | HG02647.hp1 HG02896.hp1 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.411+890A>G | MFN1 | ENSG00000171109.19 | transcript | ENST00000471841.6 | protein_coding | 4/17 | chr3 | 179359892 | ||||||
chr3:179359912
|
A | T | 1 | a0005c0010t0032g0208 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.411+910A>T | MFN1 | ENSG00000171109.19 | transcript | ENST00000471841.6 | protein_coding | 4/17 | chr3 | 179359912 | ||||||
chr3:179359973
|
CA | C | 67 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0018others(64): Show | 83 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(80): Show |
intron_variant | MODIFIER | c.411+973delA | MFN1 | ENSG00000171109.19 | transcript | ENST00000471841.6 | protein_coding | 4/17 | INFO_REALIGN_3_PRIME | chr3 | 179359973 | |||||
chr3:179359977
|
G | T | 67 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0018others(64): Show | 83 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(80): Show |
intron_variant | MODIFIER | c.411+975G>T | MFN1 | ENSG00000171109.19 | transcript | ENST00000471841.6 | protein_coding | 4/17 | chr3 | 179359977 | ||||||
chr3:179360040
|
C | T | 13 | a0001c0001t0001g0011a0001c0001t0001g0030a0001c0001t0001g0031others(10): Show | 17 | HG00544.hp2 HG00597.hp2 HG00621.hp1 others(14): Show |
intron_variant | MODIFIER | c.411+1038C>T | MFN1 | ENSG00000171109.19 | transcript | ENST00000471841.6 | protein_coding | 4/17 | chr3 | 179360040 | ||||||
chr3:179360130
|
G | A | 6 | a0001c0002t0004g0282a0001c0002t0004g0285a0001c0002t0016g0281others(3): Show | 6 | HG03669.hp1 HG03688.hp2 HG03704.hp1 others(3): Show |
intron_variant | MODIFIER | c.411+1128G>A | MFN1 | ENSG00000171109.19 | transcript | ENST00000471841.6 | protein_coding | 4/17 | chr3 | 179360130 | ||||||
chr3:179360373
|
A | G | 17 | a0001c0001t0006g0009a0001c0001t0006g0020a0001c0001t0006g0047others(14): Show | 22 | HG01069.hp2 HG01071.hp1 HG01175.hp1 others(19): Show |
intron_variant | MODIFIER | c.411+1371A>G | MFN1 | ENSG00000171109.19 | transcript | ENST00000471841.6 | protein_coding | 4/17 | chr3 | 179360373 | ||||||
chr3:179360476
|
A | T | 1 | a0001c0001t0007g0261 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.411+1474A>T | MFN1 | ENSG00000171109.19 | transcript | ENST00000471841.6 | protein_coding | 4/17 | chr3 | 179360476 | ||||||
chr3:179360527
|
A | C | 5 | a0001c0001t0020g0101a0001c0001t0020g0102a0001c0001t0020g0216others(2): Show | 5 | HG01433.hp1 HG02257.hp1 HG02280.hp1 others(2): Show |
intron_variant | MODIFIER | c.411+1525A>C | MFN1 | ENSG00000171109.19 | transcript | ENST00000471841.6 | protein_coding | 4/17 | chr3 | 179360527 | ||||||
chr3:179360549
|
CA | C | 242 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0018others(239): Show | 291 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(288): Show |
intron_variant | MODIFIER | c.411+1562delA | MFN1 | ENSG00000171109.19 | transcript | ENST00000471841.6 | protein_coding | 4/17 | INFO_REALIGN_3_PRIME | chr3 | 179360549 | |||||
chr3:179360558
|
A | T | 48 | a0001c0001t0006g0009a0001c0001t0006g0020a0001c0001t0006g0047others(45): Show | 56 | HG00735.hp2 HG01069.hp1 HG01069.hp2 others(53): Show |
intron_variant | MODIFIER | c.411+1556A>T | MFN1 | ENSG00000171109.19 | transcript | ENST00000471841.6 | protein_coding | 4/17 | chr3 | 179360558 | ||||||
chr3:179360560
|
A | T | 77 | a0001c0001t0002g0003a0001c0001t0002g0005a0001c0001t0002g0006others(74): Show | 90 | HG00140.hp2 HG00280.hp1 HG00408.hp2 others(87): Show |
intron_variant | MODIFIER | c.411+1558A>T | MFN1 | ENSG00000171109.19 | transcript | ENST00000471841.6 | protein_coding | 4/17 | chr3 | 179360560 | ||||||
chr3:179360613
|
G | T | 4 | a0001c0001t0019g0054a0001c0001t0019g0106a0001c0001t0035g0103others(1): Show | 4 | HG02647.hp1 HG02896.hp1 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.411+1611G>T | MFN1 | ENSG00000171109.19 | transcript | ENST00000471841.6 | protein_coding | 4/17 | chr3 | 179360613 | ||||||
chr3:179360644
|
G | A | 17 | a0001c0001t0006g0009a0001c0001t0006g0020a0001c0001t0006g0047others(14): Show | 22 | HG01069.hp2 HG01071.hp1 HG01175.hp1 others(19): Show |
intron_variant | MODIFIER | c.411+1642G>A | MFN1 | ENSG00000171109.19 | transcript | ENST00000471841.6 | protein_coding | 4/17 | chr3 | 179360644 | ||||||
chr3:179360672
|
T | C | 2 | a0001c0005t0027g0287a0001c0005t0027g0288 | 2 | HG02559.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.411+1670T>C | MFN1 | ENSG00000171109.19 | transcript | ENST00000471841.6 | protein_coding | 4/17 | chr3 | 179360672 | ||||||
chr3:179360740
|
GTTC | G | 24 | a0001c0001t0009g0024a0001c0001t0009g0025a0001c0001t0009g0057others(21): Show | 26 | HG00735.hp2 HG01069.hp1 HG01167.hp1 others(23): Show |
intron_variant | MODIFIER | c.412-1612_412-1610d others(5): Show |
MFN1 | ENSG00000171109.19 | transcript | ENST00000471841.6 | protein_coding | 4/17 | INFO_REALIGN_3_PRIME | chr3 | 179360740 | |||||
chr3:179361170
|
T | C | 10 | a0001c0001t0014g0014a0001c0001t0014g0070a0001c0001t0014g0071others(7): Show | 11 | HG00280.hp2 HG00323.hp2 HG01928.hp1 others(8): Show |
intron_variant | MODIFIER | c.412-1188T>C | MFN1 | ENSG00000171109.19 | transcript | ENST00000471841.6 | protein_coding | 4/17 | chr3 | 179361170 | ||||||
chr3:179361366
|
G | A | 247 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0018others(244): Show | 296 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(293): Show |
intron_variant | MODIFIER | c.412-992G>A | MFN1 | ENSG00000171109.19 | transcript | ENST00000471841.6 | protein_coding | 4/17 | chr3 | 179361366 | ||||||
chr3:179361538
|
C | CT | 8 | a0001c0001t0001g0019a0001c0001t0001g0260a0001c0001t0007g0019others(5): Show | 9 | HG01346.hp1 HG01496.hp1 HG01952.hp1 others(6): Show |
intron_variant | MODIFIER | c.412-805dupT | MFN1 | ENSG00000171109.19 | transcript | ENST00000471841.6 | protein_coding | 4/17 | INFO_REALIGN_3_PRIME | chr3 | 179361538 | |||||
chr3:179361538
|
C | CTT | 8 | a0001c0002t0004g0282a0001c0002t0004g0285a0001c0002t0016g0281others(5): Show | 8 | HG02559.hp2 HG03669.hp1 HG03688.hp2 others(5): Show |
intron_variant | MODIFIER | c.412-806_412-805dup others(2): Show |
MFN1 | ENSG00000171109.19 | transcript | ENST00000471841.6 | protein_coding | 4/17 | INFO_REALIGN_3_PRIME | chr3 | 179361538 | |||||
chr3:179361624
|
C | T | 24 | a0001c0001t0006g0009a0001c0001t0006g0020a0001c0001t0006g0047others(21): Show | 30 | HG01069.hp2 HG01071.hp1 HG01167.hp2 others(27): Show |
intron_variant | MODIFIER | c.412-734C>T | MFN1 | ENSG00000171109.19 | transcript | ENST00000471841.6 | protein_coding | 4/17 | chr3 | 179361624 | ||||||
chr3:179361657
|
C | T | 5 | a0001c0001t0020g0101a0001c0001t0020g0102a0001c0001t0020g0216others(2): Show | 5 | HG01433.hp1 HG02257.hp1 HG02280.hp1 others(2): Show |
intron_variant | MODIFIER | c.412-701C>T | MFN1 | ENSG00000171109.19 | transcript | ENST00000471841.6 | protein_coding | 4/17 | chr3 | 179361657 | ||||||
chr3:179361660
|
C | A | 1 | a0001c0001t0004g0026 | 2 | NA18612.hp1 NA18990.hp2 |
intron_variant | MODIFIER | c.412-698C>A | MFN1 | ENSG00000171109.19 | transcript | ENST00000471841.6 | protein_coding | 4/17 | chr3 | 179361660 | ||||||
chr3:179361767
|
A | G | 5 | a0001c0001t0020g0101a0001c0001t0020g0102a0001c0001t0020g0216others(2): Show | 5 | HG01433.hp1 HG02257.hp1 HG02280.hp1 others(2): Show |
intron_variant | MODIFIER | c.412-591A>G | MFN1 | ENSG00000171109.19 | transcript | ENST00000471841.6 | protein_coding | 4/17 | chr3 | 179361767 | ||||||
chr3:179361828
|
G | A | 5 | a0001c0001t0020g0101a0001c0001t0020g0102a0001c0001t0020g0216others(2): Show | 5 | HG01433.hp1 HG02257.hp1 HG02280.hp1 others(2): Show |
intron_variant | MODIFIER | c.412-530G>A | MFN1 | ENSG00000171109.19 | transcript | ENST00000471841.6 | protein_coding | 4/17 | chr3 | 179361828 | ||||||
chr3:179361855
|
C | G | 1 | a0001c0001t0003g0272 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.412-503C>G | MFN1 | ENSG00000171109.19 | transcript | ENST00000471841.6 | protein_coding | 4/17 | chr3 | 179361855 | ||||||
chr3:179361903
|
G | A | 1 | a0001c0001t0035g0103 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.412-455G>A | MFN1 | ENSG00000171109.19 | transcript | ENST00000471841.6 | protein_coding | 4/17 | chr3 | 179361903 | ||||||
chr3:179361961
|
A | G | 1 | a0001c0001t0031g0132 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.412-397A>G | MFN1 | ENSG00000171109.19 | transcript | ENST00000471841.6 | protein_coding | 4/17 | chr3 | 179361961 | ||||||
chr3:179362111
|
T | C | 1 | a0001c0001t0001g0231 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.412-247T>C | MFN1 | ENSG00000171109.19 | transcript | ENST00000471841.6 | protein_coding | 4/17 | chr3 | 179362111 | ||||||
chr3:179362491
|
A | G | 1 | a0001c0001t0001g0144 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.536+9A>G | MFN1 | ENSG00000171109.19 | transcript | ENST00000471841.6 | protein_coding | 5/17 | chr3 | 179362491 | ||||||
chr3:179362637
|
A | G | 2 | a0001c0001t0001g0242a0001c0001t0001g0256 | 2 | NA18962.hp1 NA19057.hp1 |
intron_variant | MODIFIER | c.536+155A>G | MFN1 | ENSG00000171109.19 | transcript | ENST00000471841.6 | protein_coding | 5/17 | chr3 | 179362637 | ||||||
chr3:179362727
|
G | A | 17 | a0001c0001t0006g0009a0001c0001t0006g0020a0001c0001t0006g0047others(14): Show | 22 | HG01069.hp2 HG01071.hp1 HG01175.hp1 others(19): Show |
intron_variant | MODIFIER | c.536+245G>A | MFN1 | ENSG00000171109.19 | transcript | ENST00000471841.6 | protein_coding | 5/17 | chr3 | 179362727 | ||||||
chr3:179362794
|
C | G | 1 | a0001c0001t0001g0255 | 1 | NA19055.hp1 | intron_variant | MODIFIER | c.536+312C>G | MFN1 | ENSG00000171109.19 | transcript | ENST00000471841.6 | protein_coding | 5/17 | chr3 | 179362794 | ||||||
chr3:179362820
|
C | T | 3 | a0001c0001t0020g0101a0001c0001t0020g0102a0001c0001t0020g0216 | 3 | HG01433.hp1 HG02280.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.536+338C>T | MFN1 | ENSG00000171109.19 | transcript | ENST00000471841.6 | protein_coding | 5/17 | chr3 | 179362820 | ||||||
chr3:179363007
|
C | A | 8 | a0001c0001t0001g0007a0001c0001t0001g0043a0001c0001t0001g0243others(5): Show | 13 | HG00099.hp1 HG00099.hp2 HG00639.hp2 others(10): Show |
intron_variant | MODIFIER | c.536+525C>A | MFN1 | ENSG00000171109.19 | transcript | ENST00000471841.6 | protein_coding | 5/17 | chr3 | 179363007 | ||||||
chr3:179363086
|
G | A | 6 | a0001c0001t0015g0021a0001c0001t0015g0299a0001c0001t0015g0300others(3): Show | 7 | HG01167.hp2 HG01169.hp1 HG02109.hp1 others(4): Show |
intron_variant | MODIFIER | c.536+604G>A | MFN1 | ENSG00000171109.19 | transcript | ENST00000471841.6 | protein_coding | 5/17 | chr3 | 179363086 | ||||||
chr3:179363158
|
C | T | 39 | a0001c0001t0004g0001a0001c0001t0004g0026a0001c0001t0004g0069others(36): Show | 51 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(48): Show |
intron_variant | MODIFIER | c.536+676C>T | MFN1 | ENSG00000171109.19 | transcript | ENST00000471841.6 | protein_coding | 5/17 | chr3 | 179363158 | ||||||
chr3:179363183
|
A | G | 1 | a0001c0001t0001g0031 | 2 | HG00597.hp2 HG00621.hp1 |
intron_variant | MODIFIER | c.536+701A>G | MFN1 | ENSG00000171109.19 | transcript | ENST00000471841.6 | protein_coding | 5/17 | chr3 | 179363183 | ||||||
chr3:179363244
|
C | G | 1 | a0001c0009t0039g0225 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.536+762C>G | MFN1 | ENSG00000171109.19 | transcript | ENST00000471841.6 | protein_coding | 5/17 | chr3 | 179363244 | ||||||
chr3:179363257
|
G | C | 8 | a0001c0001t0009g0024a0001c0001t0009g0057a0001c0001t0009g0058others(5): Show | 8 | HG02572.hp2 HG02630.hp2 HG02818.hp1 others(5): Show |
intron_variant | MODIFIER | c.536+775G>C | MFN1 | ENSG00000171109.19 | transcript | ENST00000471841.6 | protein_coding | 5/17 | chr3 | 179363257 | ||||||
chr3:179363261
|
T | G | 1 | a0001c0001t0002g0194 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.536+779T>G | MFN1 | ENSG00000171109.19 | transcript | ENST00000471841.6 | protein_coding | 5/17 | chr3 | 179363261 | ||||||
chr3:179363394
|
A | G | 6 | a0001c0001t0015g0021a0001c0001t0015g0299a0001c0001t0015g0300others(3): Show | 7 | HG01167.hp2 HG01169.hp1 HG02109.hp1 others(4): Show |
intron_variant | MODIFIER | c.537-903A>G | MFN1 | ENSG00000171109.19 | transcript | ENST00000471841.6 | protein_coding | 5/17 | chr3 | 179363394 | ||||||
chr3:179363479
|
C | G | 1 | a0001c0001t0001g0043 | 2 | HG00099.hp1 HG00733.hp1 |
intron_variant | MODIFIER | c.537-818C>G | MFN1 | ENSG00000171109.19 | transcript | ENST00000471841.6 | protein_coding | 5/17 | chr3 | 179363479 | ||||||
chr3:179363494
|
A | AT | 7 | a0001c0001t0018g0022a0001c0001t0018g0050a0001c0001t0018g0052others(4): Show | 8 | HG01069.hp1 HG01167.hp1 HG01884.hp1 others(5): Show |
intron_variant | MODIFIER | c.537-790dupT | MFN1 | ENSG00000171109.19 | transcript | ENST00000471841.6 | protein_coding | 5/17 | INFO_REALIGN_3_PRIME | chr3 | 179363494 | |||||
chr3:179363682
|
C | T | 1 | a0001c0001t0001g0255 | 1 | NA19055.hp1 | intron_variant | MODIFIER | c.537-615C>T | MFN1 | ENSG00000171109.19 | transcript | ENST00000471841.6 | protein_coding | 5/17 | chr3 | 179363682 | ||||||
chr3:179363836
|
A | G | 2 | a0001c0001t0003g0271a0001c0001t0003g0272 | 2 | NA19240.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.537-461A>G | MFN1 | ENSG00000171109.19 | transcript | ENST00000471841.6 | protein_coding | 5/17 | chr3 | 179363836 | ||||||
chr3:179363875
|
T | C | 246 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0018others(243): Show | 295 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(292): Show |
intron_variant | MODIFIER | c.537-422T>C | MFN1 | ENSG00000171109.19 | transcript | ENST00000471841.6 | protein_coding | 5/17 | chr3 | 179363875 | ||||||
chr3:179364041
|
C | A | 1 | a0001c0001t0001g0226 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.537-256C>A | MFN1 | ENSG00000171109.19 | transcript | ENST00000471841.6 | protein_coding | 5/17 | chr3 | 179364041 | ||||||
chr3:179364064
|
G | T | 1 | a0001c0001t0001g0043 | 2 | HG00099.hp1 HG00733.hp1 |
intron_variant | MODIFIER | c.537-233G>T | MFN1 | ENSG00000171109.19 | transcript | ENST00000471841.6 | protein_coding | 5/17 | chr3 | 179364064 | ||||||
chr3:179364124
|
A | T | 34 | a0001c0001t0004g0001a0001c0001t0004g0026a0001c0001t0004g0069others(31): Show | 46 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(43): Show |
intron_variant | MODIFIER | c.537-173A>T | MFN1 | ENSG00000171109.19 | transcript | ENST00000471841.6 | protein_coding | 5/17 | chr3 | 179364124 | ||||||
chr3:179364211
|
A | C | 1 | a0001c0001t0017g0093 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.537-86A>C | MFN1 | ENSG00000171109.19 | transcript | ENST00000471841.6 | protein_coding | 5/17 | chr3 | 179364211 | ||||||
chr3:179364534
|
G | T | 17 | a0001c0001t0006g0009a0001c0001t0006g0020a0001c0001t0006g0047others(14): Show | 22 | HG01069.hp2 HG01071.hp1 HG01175.hp1 others(19): Show |
intron_variant | MODIFIER | c.645+129G>T | MFN1 | ENSG00000171109.19 | transcript | ENST00000471841.6 | protein_coding | 6/17 | chr3 | 179364534 | ||||||
chr3:179364535
|
G | A | 2 | a0001c0001t0001g0109a0001c0001t0003g0110 | 2 | NA18961.hp2 NA18978.hp1 |
intron_variant | MODIFIER | c.645+130G>A | MFN1 | ENSG00000171109.19 | transcript | ENST00000471841.6 | protein_coding | 6/17 | chr3 | 179364535 | ||||||
chr3:179364730
|
G | A | 1 | a0001c0001t0005g0162 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.645+325G>A | MFN1 | ENSG00000171109.19 | transcript | ENST00000471841.6 | protein_coding | 6/17 | chr3 | 179364730 | ||||||
chr3:179364781
|
A | G | 6 | a0001c0001t0018g0022a0001c0001t0018g0050a0001c0001t0018g0052others(3): Show | 7 | HG01069.hp1 HG01167.hp1 HG01884.hp1 others(4): Show |
intron_variant | MODIFIER | c.646-337A>G | MFN1 | ENSG00000171109.19 | transcript | ENST00000471841.6 | protein_coding | 6/17 | chr3 | 179364781 | ||||||
chr3:179364864
|
A | T | 6 | a0001c0002t0004g0282a0001c0002t0004g0285a0001c0002t0016g0281others(3): Show | 6 | HG03669.hp1 HG03688.hp2 HG03704.hp1 others(3): Show |
intron_variant | MODIFIER | c.646-254A>T | MFN1 | ENSG00000171109.19 | transcript | ENST00000471841.6 | protein_coding | 6/17 | chr3 | 179364864 | ||||||
chr3:179364897
|
T | C | 1 | a0001c0001t0001g0144 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.646-221T>C | MFN1 | ENSG00000171109.19 | transcript | ENST00000471841.6 | protein_coding | 6/17 | chr3 | 179364897 | ||||||
chr3:179364927
|
T | C | 1 | a0005c0010t0032g0208 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.646-191T>C | MFN1 | ENSG00000171109.19 | transcript | ENST00000471841.6 | protein_coding | 6/17 | chr3 | 179364927 | ||||||
chr3:179364939
|
T | C | 1 | a0001c0001t0001g0120 | 1 | NA18980.hp2 | intron_variant | MODIFIER | c.646-179T>C | MFN1 | ENSG00000171109.19 | transcript | ENST00000471841.6 | protein_coding | 6/17 | chr3 | 179364939 | ||||||
chr3:179365291
|
C | T | 67 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0018others(64): Show | 83 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(80): Show |
intron_variant | MODIFIER | c.753+66C>T | MFN1 | ENSG00000171109.19 | transcript | ENST00000471841.6 | protein_coding | 7/17 | chr3 | 179365291 | ||||||
chr3:179365293
|
A | G | 5 | a0001c0001t0020g0101a0001c0001t0020g0102a0001c0001t0020g0216others(2): Show | 5 | HG01433.hp1 HG02257.hp1 HG02280.hp1 others(2): Show |
intron_variant | MODIFIER | c.753+68A>G | MFN1 | ENSG00000171109.19 | transcript | ENST00000471841.6 | protein_coding | 7/17 | chr3 | 179365293 | ||||||
chr3:179365656
|
C | T | 8 | a0001c0001t0009g0024a0001c0001t0009g0057a0001c0001t0009g0058others(5): Show | 8 | HG02572.hp2 HG02630.hp2 HG02818.hp1 others(5): Show |
intron_variant | MODIFIER | c.753+431C>T | MFN1 | ENSG00000171109.19 | transcript | ENST00000471841.6 | protein_coding | 7/17 | chr3 | 179365656 | ||||||
chr3:179365670
|
C | G | 1 | a0001c0001t0004g0086 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.753+445C>G | MFN1 | ENSG00000171109.19 | transcript | ENST00000471841.6 | protein_coding | 7/17 | chr3 | 179365670 | ||||||
chr3:179365967
|
C | T | 1 | a0001c0001t0036g0210 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.753+742C>T | MFN1 | ENSG00000171109.19 | transcript | ENST00000471841.6 | protein_coding | 7/17 | chr3 | 179365967 | ||||||
chr3:179366089
|
T | C | 1 | a0001c0001t0001g0131 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.753+864T>C | MFN1 | ENSG00000171109.19 | transcript | ENST00000471841.6 | protein_coding | 7/17 | chr3 | 179366089 | ||||||
chr3:179366209
|
A | C | 6 | a0001c0001t0015g0021a0001c0001t0015g0299a0001c0001t0015g0300others(3): Show | 7 | HG01167.hp2 HG01169.hp1 HG02109.hp1 others(4): Show |
intron_variant | MODIFIER | c.753+984A>C | MFN1 | ENSG00000171109.19 | transcript | ENST00000471841.6 | protein_coding | 7/17 | chr3 | 179366209 | ||||||
chr3:179366241
|
T | G | 1 | a0001c0001t0011g0163 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.753+1016T>G | MFN1 | ENSG00000171109.19 | transcript | ENST00000471841.6 | protein_coding | 7/17 | chr3 | 179366241 | ||||||
chr3:179366258
|
C | T | 53 | a0001c0001t0006g0009a0001c0001t0006g0020a0001c0001t0006g0047others(50): Show | 61 | HG00735.hp2 HG01069.hp1 HG01069.hp2 others(58): Show |
intron_variant | MODIFIER | c.753+1033C>T | MFN1 | ENSG00000171109.19 | transcript | ENST00000471841.6 | protein_coding | 7/17 | chr3 | 179366258 | ||||||
chr3:179366385
|
CT | C | 42 | a0001c0001t0001g0246a0001c0001t0004g0001a0001c0001t0004g0026others(39): Show | 55 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(52): Show |
intron_variant | MODIFIER | c.754-1040delT | MFN1 | ENSG00000171109.19 | transcript | ENST00000471841.6 | protein_coding | 7/17 | INFO_REALIGN_3_PRIME | chr3 | 179366385 | |||||
chr3:179366548
|
T | A | 2 | a0001c0001t0016g0080a0001c0001t0016g0082 | 2 | HG01070.hp1 HG01071.hp2 |
intron_variant | MODIFIER | c.754-891T>A | MFN1 | ENSG00000171109.19 | transcript | ENST00000471841.6 | protein_coding | 7/17 | chr3 | 179366548 | ||||||
chr3:179366654
|
T | G | 6 | a0001c0001t0015g0021a0001c0001t0015g0299a0001c0001t0015g0300others(3): Show | 7 | HG01167.hp2 HG01169.hp1 HG02109.hp1 others(4): Show |
intron_variant | MODIFIER | c.754-785T>G | MFN1 | ENSG00000171109.19 | transcript | ENST00000471841.6 | protein_coding | 7/17 | chr3 | 179366654 | ||||||
chr3:179366952
|
G | T | 1 | a0001c0001t0002g0036 | 2 | NA18974.hp2 NA19054.hp1 |
intron_variant | MODIFIER | c.754-487G>T | MFN1 | ENSG00000171109.19 | transcript | ENST00000471841.6 | protein_coding | 7/17 | chr3 | 179366952 | ||||||
chr3:179366987
|
G | C | 1 | a0001c0001t0001g0237 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.754-452G>C | MFN1 | ENSG00000171109.19 | transcript | ENST00000471841.6 | protein_coding | 7/17 | chr3 | 179366987 | ||||||
chr3:179367001
|
C | T | 8 | a0001c0002t0004g0282a0001c0002t0004g0285a0001c0002t0016g0281others(5): Show | 8 | HG02559.hp2 HG03669.hp1 HG03688.hp2 others(5): Show |
intron_variant | MODIFIER | c.754-438C>T | MFN1 | ENSG00000171109.19 | transcript | ENST00000471841.6 | protein_coding | 7/17 | chr3 | 179367001 | ||||||
chr3:179367073
|
A | G | 129 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0018others(126): Show | 153 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(150): Show |
intron_variant | MODIFIER | c.754-366A>G | MFN1 | ENSG00000171109.19 | transcript | ENST00000471841.6 | protein_coding | 7/17 | chr3 | 179367073 | ||||||
chr3:179367084
|
C | T | 1 | a0001c0001t0001g0144 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.754-355C>T | MFN1 | ENSG00000171109.19 | transcript | ENST00000471841.6 | protein_coding | 7/17 | chr3 | 179367084 | ||||||
chr3:179367145
|
C | T | 1 | a0001c0001t0036g0210 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.754-294C>T | MFN1 | ENSG00000171109.19 | transcript | ENST00000471841.6 | protein_coding | 7/17 | chr3 | 179367145 | ||||||
chr3:179367165
|
A | C | 6 | a0001c0002t0004g0282a0001c0002t0004g0285a0001c0002t0016g0281others(3): Show | 6 | HG03669.hp1 HG03688.hp2 HG03704.hp1 others(3): Show |
intron_variant | MODIFIER | c.754-274A>C | MFN1 | ENSG00000171109.19 | transcript | ENST00000471841.6 | protein_coding | 7/17 | chr3 | 179367165 | ||||||
chr3:179367172
|
C | T | 1 | a0001c0001t0006g0297 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.754-267C>T | MFN1 | ENSG00000171109.19 | transcript | ENST00000471841.6 | protein_coding | 7/17 | chr3 | 179367172 | ||||||
chr3:179367648
|
G | T | 1 | a0001c0001t0008g0189 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.907+56G>T | MFN1 | ENSG00000171109.19 | transcript | ENST00000471841.6 | protein_coding | 8/17 | chr3 | 179367648 | ||||||
chr3:179367726
|
C | G | 79 | a0001c0001t0002g0003a0001c0001t0002g0005a0001c0001t0002g0006others(76): Show | 92 | HG00140.hp2 HG00280.hp1 HG00408.hp2 others(89): Show |
intron_variant | MODIFIER | c.907+134C>G | MFN1 | ENSG00000171109.19 | transcript | ENST00000471841.6 | protein_coding | 8/17 | chr3 | 179367726 | ||||||
chr3:179367789
|
G | T | 2 | a0001c0001t0023g0303a0001c0001t0023g0304 | 2 | HG02257.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.907+197G>T | MFN1 | ENSG00000171109.19 | transcript | ENST00000471841.6 | protein_coding | 8/17 | chr3 | 179367789 | ||||||
chr3:179367802
|
A | C | 1 | a0005c0010t0032g0208 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.907+210A>C | MFN1 | ENSG00000171109.19 | transcript | ENST00000471841.6 | protein_coding | 8/17 | chr3 | 179367802 | ||||||
chr3:179367817
|
G | C | 41 | a0001c0001t0001g0144a0001c0001t0004g0001a0001c0001t0004g0026others(38): Show | 53 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(50): Show |
intron_variant | MODIFIER | c.908-219G>C | MFN1 | ENSG00000171109.19 | transcript | ENST00000471841.6 | protein_coding | 8/17 | chr3 | 179367817 | ||||||
chr3:179367842
|
G | A | 8 | a0001c0001t0001g0049a0001c0001t0001g0134a0001c0001t0001g0217others(5): Show | 8 | HG00735.hp1 HG01256.hp2 HG01258.hp1 others(5): Show |
intron_variant | MODIFIER | c.908-194G>A | MFN1 | ENSG00000171109.19 | transcript | ENST00000471841.6 | protein_coding | 8/17 | chr3 | 179367842 | ||||||
chr3:179367866
|
C | T | 6 | a0001c0001t0001g0049a0001c0001t0001g0217a0001c0001t0003g0133others(3): Show | 6 | HG00735.hp1 HG01256.hp2 HG01258.hp1 others(3): Show |
intron_variant | MODIFIER | c.908-170C>T | MFN1 | ENSG00000171109.19 | transcript | ENST00000471841.6 | protein_coding | 8/17 | chr3 | 179367866 | ||||||
chr3:179367928
|
G | A | 66 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0018others(63): Show | 82 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(79): Show |
intron_variant | MODIFIER | c.908-108G>A | MFN1 | ENSG00000171109.19 | transcript | ENST00000471841.6 | protein_coding | 8/17 | chr3 | 179367928 | ||||||
chr3:179367931
|
A | T | 1 | a0001c0001t0001g0215 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.908-105A>T | MFN1 | ENSG00000171109.19 | transcript | ENST00000471841.6 | protein_coding | 8/17 | chr3 | 179367931 | ||||||
chr3:179367934
|
G | GTA | 139 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0018others(136): Show | 165 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(162): Show |
intron_variant | MODIFIER | c.908-84_908-83dupAT | MFN1 | ENSG00000171109.19 | transcript | ENST00000471841.6 | protein_coding | 8/17 | INFO_REALIGN_3_PRIME | chr3 | 179367934 | |||||
chr3:179367934
|
G | GTATA | 36 | a0001c0001t0002g0005a0001c0001t0002g0147a0001c0001t0002g0160others(33): Show | 45 | HG00408.hp2 HG00423.hp1 HG01069.hp2 others(42): Show |
intron_variant | MODIFIER | c.908-86_908-83dupAT others(2): Show |
MFN1 | ENSG00000171109.19 | transcript | ENST00000471841.6 | protein_coding | 8/17 | INFO_REALIGN_3_PRIME | chr3 | 179367934 | |||||
chr3:179367987
|
C | T | 66 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0018others(63): Show | 82 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(79): Show |
intron_variant | MODIFIER | c.908-49C>T | MFN1 | ENSG00000171109.19 | transcript | ENST00000471841.6 | protein_coding | 8/17 | chr3 | 179367987 | ||||||
chr3:179367991
|
T | C | 8 | a0001c0001t0001g0049a0001c0001t0001g0134a0001c0001t0001g0217others(5): Show | 8 | HG00735.hp1 HG01256.hp2 HG01258.hp1 others(5): Show |
intron_variant | MODIFIER | c.908-45T>C | MFN1 | ENSG00000171109.19 | transcript | ENST00000471841.6 | protein_coding | 8/17 | chr3 | 179367991 | ||||||
chr3:179368003
|
C | T | 53 | a0001c0001t0006g0009a0001c0001t0006g0020a0001c0001t0006g0047others(50): Show | 61 | HG00735.hp2 HG01069.hp1 HG01069.hp2 others(58): Show |
intron_variant | MODIFIER | c.908-33C>T | MFN1 | ENSG00000171109.19 | transcript | ENST00000471841.6 | protein_coding | 8/17 | chr3 | 179368003 | ||||||
chr3:179368210
|
A | G | 17 | a0001c0001t0006g0009a0001c0001t0006g0020a0001c0001t0006g0047others(14): Show | 22 | HG01069.hp2 HG01071.hp1 HG01175.hp1 others(19): Show |
intron_variant | MODIFIER | c.975+107A>G | MFN1 | ENSG00000171109.19 | transcript | ENST00000471841.6 | protein_coding | 9/17 | chr3 | 179368210 | ||||||
chr3:179368245
|
G | A | 1 | a0001c0001t0005g0098 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.975+142G>A | MFN1 | ENSG00000171109.19 | transcript | ENST00000471841.6 | protein_coding | 9/17 | chr3 | 179368245 | ||||||
chr3:179368308
|
T | C | 1 | a0001c0001t0001g0138 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.975+205T>C | MFN1 | ENSG00000171109.19 | transcript | ENST00000471841.6 | protein_coding | 9/17 | chr3 | 179368308 | ||||||
chr3:179368458
|
CA | C | 8 | a0001c0002t0004g0282a0001c0002t0004g0285a0001c0002t0016g0281others(5): Show | 8 | HG02559.hp2 HG03669.hp1 HG03688.hp2 others(5): Show |
intron_variant | MODIFIER | c.975+358delA | MFN1 | ENSG00000171109.19 | transcript | ENST00000471841.6 | protein_coding | 9/17 | INFO_REALIGN_3_PRIME | chr3 | 179368458 | |||||
chr3:179368709
|
G | A | 5 | a0001c0001t0020g0101a0001c0001t0020g0102a0001c0001t0020g0216others(2): Show | 5 | HG01433.hp1 HG02257.hp1 HG02280.hp1 others(2): Show |
intron_variant | MODIFIER | c.975+606G>A | MFN1 | ENSG00000171109.19 | transcript | ENST00000471841.6 | protein_coding | 9/17 | chr3 | 179368709 | ||||||
chr3:179368905
|
A | G | 1 | a0001c0001t0038g0294 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.975+802A>G | MFN1 | ENSG00000171109.19 | transcript | ENST00000471841.6 | protein_coding | 9/17 | chr3 | 179368905 | ||||||
chr3:179368915
|
G | T | 1 | a0001c0001t0038g0294 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.975+812G>T | MFN1 | ENSG00000171109.19 | transcript | ENST00000471841.6 | protein_coding | 9/17 | chr3 | 179368915 | ||||||
chr3:179368996
|
G | A | 4 | a0001c0001t0015g0021a0001c0001t0015g0301a0001c0001t0015g0302others(1): Show | 5 | HG02109.hp1 HG02615.hp1 HG02809.hp2 others(2): Show |
intron_variant | MODIFIER | c.975+893G>A | MFN1 | ENSG00000171109.19 | transcript | ENST00000471841.6 | protein_coding | 9/17 | chr3 | 179368996 | ||||||
chr3:179369066
|
A | T | 6 | a0001c0002t0004g0282a0001c0002t0004g0285a0001c0002t0016g0281others(3): Show | 6 | HG03669.hp1 HG03688.hp2 HG03704.hp1 others(3): Show |
intron_variant | MODIFIER | c.975+963A>T | MFN1 | ENSG00000171109.19 | transcript | ENST00000471841.6 | protein_coding | 9/17 | chr3 | 179369066 | ||||||
chr3:179369149
|
A | G | 8 | a0001c0002t0004g0282a0001c0002t0004g0285a0001c0002t0016g0281others(5): Show | 8 | HG02559.hp2 HG03669.hp1 HG03688.hp2 others(5): Show |
intron_variant | MODIFIER | c.975+1046A>G | MFN1 | ENSG00000171109.19 | transcript | ENST00000471841.6 | protein_coding | 9/17 | chr3 | 179369149 | ||||||
chr3:179369215
|
C | CT | 53 | a0001c0001t0006g0009a0001c0001t0006g0020a0001c0001t0006g0047others(50): Show | 61 | HG00735.hp2 HG01069.hp1 HG01069.hp2 others(58): Show |
intron_variant | MODIFIER | c.975+1118dupT | MFN1 | ENSG00000171109.19 | transcript | ENST00000471841.6 | protein_coding | 9/17 | INFO_REALIGN_3_PRIME | chr3 | 179369215 | |||||
chr3:179369284
|
G | A | 67 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0018others(64): Show | 83 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(80): Show |
intron_variant | MODIFIER | c.975+1181G>A | MFN1 | ENSG00000171109.19 | transcript | ENST00000471841.6 | protein_coding | 9/17 | chr3 | 179369284 | ||||||
chr3:179369316
|
A | G | 34 | a0001c0001t0004g0001a0001c0001t0004g0026a0001c0001t0004g0069others(31): Show | 46 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(43): Show |
intron_variant | MODIFIER | c.975+1213A>G | MFN1 | ENSG00000171109.19 | transcript | ENST00000471841.6 | protein_coding | 9/17 | chr3 | 179369316 | ||||||
chr3:179369455
|
T | C | 8 | a0001c0002t0004g0282a0001c0002t0004g0285a0001c0002t0016g0281others(5): Show | 8 | HG02559.hp2 HG03669.hp1 HG03688.hp2 others(5): Show |
intron_variant | MODIFIER | c.975+1352T>C | MFN1 | ENSG00000171109.19 | transcript | ENST00000471841.6 | protein_coding | 9/17 | chr3 | 179369455 | ||||||
chr3:179369571
|
G | A | 2 | a0001c0005t0027g0287a0001c0005t0027g0288 | 2 | HG02559.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.975+1468G>A | MFN1 | ENSG00000171109.19 | transcript | ENST00000471841.6 | protein_coding | 9/17 | chr3 | 179369571 | ||||||
chr3:179369584
|
G | T | 66 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0018others(63): Show | 82 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(79): Show |
intron_variant | MODIFIER | c.975+1481G>T | MFN1 | ENSG00000171109.19 | transcript | ENST00000471841.6 | protein_coding | 9/17 | chr3 | 179369584 | ||||||
chr3:179369600
|
A | T | 1 | a0001c0001t0001g0114 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.975+1497A>T | MFN1 | ENSG00000171109.19 | transcript | ENST00000471841.6 | protein_coding | 9/17 | chr3 | 179369600 | ||||||
chr3:179369638
|
A | G | 3 | a0001c0001t0001g0107a0001c0001t0001g0113a0001c0001t0001g0127 | 3 | NA18939.hp1 NA18964.hp2 NA19060.hp1 |
intron_variant | MODIFIER | c.975+1535A>G | MFN1 | ENSG00000171109.19 | transcript | ENST00000471841.6 | protein_coding | 9/17 | chr3 | 179369638 | ||||||
chr3:179370126
|
T | C | 1 | a0001c0001t0023g0304 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.975+2023T>C | MFN1 | ENSG00000171109.19 | transcript | ENST00000471841.6 | protein_coding | 9/17 | chr3 | 179370126 | ||||||
chr3:179370171
|
G | A | 2 | a0001c0001t0023g0303a0001c0001t0023g0304 | 2 | HG02257.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.975+2068G>A | MFN1 | ENSG00000171109.19 | transcript | ENST00000471841.6 | protein_coding | 9/17 | chr3 | 179370171 | ||||||
chr3:179370240
|
C | A | 4 | a0001c0001t0014g0014a0001c0001t0014g0071a0001c0001t0014g0072others(1): Show | 5 | HG00280.hp2 HG01928.hp1 HG01993.hp2 others(2): Show |
intron_variant | MODIFIER | c.975+2137C>A | MFN1 | ENSG00000171109.19 | transcript | ENST00000471841.6 | protein_coding | 9/17 | chr3 | 179370240 | ||||||
chr3:179370332
|
C | T | 1 | a0001c0001t0013g0213 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.975+2229C>T | MFN1 | ENSG00000171109.19 | transcript | ENST00000471841.6 | protein_coding | 9/17 | chr3 | 179370332 | ||||||
chr3:179370363
|
A | G | 2 | a0001c0001t0011g0200a0001c0001t0028g0188 | 2 | HG02074.hp2 NA18994.hp2 |
intron_variant | MODIFIER | c.975+2260A>G | MFN1 | ENSG00000171109.19 | transcript | ENST00000471841.6 | protein_coding | 9/17 | chr3 | 179370363 | ||||||
chr3:179370392
|
C | CT | 93 | a0001c0001t0001g0143a0001c0001t0002g0003a0001c0001t0002g0005others(90): Show | 107 | HG00140.hp2 HG00408.hp2 HG00423.hp1 others(104): Show |
intron_variant | MODIFIER | c.975+2312dupT | MFN1 | ENSG00000171109.19 | transcript | ENST00000471841.6 | protein_coding | 9/17 | INFO_REALIGN_3_PRIME | chr3 | 179370392 | |||||
chr3:179370392
|
C | CTT | 16 | a0001c0001t0002g0147a0001c0001t0002g0184a0001c0001t0002g0204others(13): Show | 16 | HG01515.hp1 HG01517.hp1 HG01975.hp2 others(13): Show |
intron_variant | MODIFIER | c.975+2311_975+2312d others(4): Show |
MFN1 | ENSG00000171109.19 | transcript | ENST00000471841.6 | protein_coding | 9/17 | INFO_REALIGN_3_PRIME | chr3 | 179370392 | |||||
chr3:179370392
|
C | CTTT | 7 | a0001c0001t0011g0035a0001c0001t0011g0154a0001c0001t0011g0163others(4): Show | 8 | HG00280.hp1 HG00544.hp1 HG01257.hp2 others(5): Show |
intron_variant | MODIFIER | c.975+2310_975+2312d others(5): Show |
MFN1 | ENSG00000171109.19 | transcript | ENST00000471841.6 | protein_coding | 9/17 | INFO_REALIGN_3_PRIME | chr3 | 179370392 | |||||
chr3:179370392
|
C | CTTTTTTT others(1): Show |
30 | a0001c0001t0001g0007a0001c0001t0001g0018a0001c0001t0001g0019others(27): Show | 42 | HG00099.hp1 HG00099.hp2 HG00609.hp1 others(39): Show |
intron_variant | MODIFIER | c.975+2305_975+2312d others(10): Show |
MFN1 | ENSG00000171109.19 | transcript | ENST00000471841.6 | protein_coding | 9/17 | INFO_REALIGN_3_PRIME | chr3 | 179370392 | |||||
chr3:179370392
|
C | CTTTTTTT others(2): Show |
19 | a0001c0001t0001g0008a0001c0001t0001g0045a0001c0001t0001g0232others(16): Show | 23 | HG00408.hp1 HG00642.hp1 HG01496.hp1 others(20): Show |
intron_variant | MODIFIER | c.975+2304_975+2312d others(11): Show |
MFN1 | ENSG00000171109.19 | transcript | ENST00000471841.6 | protein_coding | 9/17 | INFO_REALIGN_3_PRIME | chr3 | 179370392 | |||||
chr3:179370392
|
C | CTTTTTTT others(3): Show |
7 | a0001c0001t0001g0260a0001c0001t0001g0269a0001c0001t0001g0270others(4): Show | 7 | HG00597.hp1 HG03654.hp1 NA18943.hp2 others(4): Show |
intron_variant | MODIFIER | c.975+2303_975+2312d others(12): Show |
MFN1 | ENSG00000171109.19 | transcript | ENST00000471841.6 | protein_coding | 9/17 | INFO_REALIGN_3_PRIME | chr3 | 179370392 | |||||
chr3:179370392
|
C | CTTTTTTT others(4): Show |
4 | a0001c0001t0001g0042a0001c0001t0001g0239a0001c0001t0031g0254others(1): Show | 4 | HG00423.hp2 HG01106.hp2 HG02273.hp1 others(1): Show |
intron_variant | MODIFIER | c.975+2302_975+2312d others(13): Show |
MFN1 | ENSG00000171109.19 | transcript | ENST00000471841.6 | protein_coding | 9/17 | INFO_REALIGN_3_PRIME | chr3 | 179370392 | |||||
chr3:179370392
|
C | T | 1 | a0001c0001t0005g0098 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.975+2289C>T | MFN1 | ENSG00000171109.19 | transcript | ENST00000471841.6 | protein_coding | 9/17 | chr3 | 179370392 | ||||||
chr3:179370392
|
CT | C | 81 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0010others(78): Show | 108 | HG00140.hp1 HG00323.hp1 HG00438.hp1 others(105): Show |
intron_variant | MODIFIER | c.975+2312delT | MFN1 | ENSG00000171109.19 | transcript | ENST00000471841.6 | protein_coding | 9/17 | INFO_REALIGN_3_PRIME | chr3 | 179370392 | |||||
chr3:179370419
|
A | G | 2 | a0001c0001t0002g0170a0001c0001t0002g0205 | 2 | NA18940.hp2 NA18988.hp1 |
intron_variant | MODIFIER | c.975+2316A>G | MFN1 | ENSG00000171109.19 | transcript | ENST00000471841.6 | protein_coding | 9/17 | chr3 | 179370419 | ||||||
chr3:179370428
|
C | T | 6 | a0001c0001t0007g0274a0001c0001t0019g0054a0001c0001t0019g0105others(3): Show | 6 | HG02647.hp1 HG02896.hp1 HG02965.hp1 others(3): Show |
intron_variant | MODIFIER | c.975+2325C>T | MFN1 | ENSG00000171109.19 | transcript | ENST00000471841.6 | protein_coding | 9/17 | chr3 | 179370428 | ||||||
chr3:179370690
|
G | C | 79 | a0001c0001t0002g0003a0001c0001t0002g0005a0001c0001t0002g0006others(76): Show | 92 | HG00140.hp2 HG00280.hp1 HG00408.hp2 others(89): Show |
intron_variant | MODIFIER | c.975+2587G>C | MFN1 | ENSG00000171109.19 | transcript | ENST00000471841.6 | protein_coding | 9/17 | chr3 | 179370690 | ||||||
chr3:179370772
|
A | G | 1 | a0001c0001t0001g0114 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.975+2669A>G | MFN1 | ENSG00000171109.19 | transcript | ENST00000471841.6 | protein_coding | 9/17 | chr3 | 179370772 | ||||||
chr3:179370842
|
TTTG | T | 3 | a0001c0001t0020g0101a0001c0001t0020g0102a0001c0001t0020g0216 | 3 | HG01433.hp1 HG02280.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.975+2745_975+2747d others(5): Show |
MFN1 | ENSG00000171109.19 | transcript | ENST00000471841.6 | protein_coding | 9/17 | INFO_REALIGN_3_PRIME | chr3 | 179370842 | |||||
chr3:179370876
|
T | C | 6 | a0001c0002t0004g0282a0001c0002t0004g0285a0001c0002t0016g0281others(3): Show | 6 | HG03669.hp1 HG03688.hp2 HG03704.hp1 others(3): Show |
intron_variant | MODIFIER | c.975+2773T>C | MFN1 | ENSG00000171109.19 | transcript | ENST00000471841.6 | protein_coding | 9/17 | chr3 | 179370876 | ||||||
chr3:179370898
|
T | C | 1 | a0001c0001t0035g0103 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.975+2795T>C | MFN1 | ENSG00000171109.19 | transcript | ENST00000471841.6 | protein_coding | 9/17 | chr3 | 179370898 | ||||||
chr3:179371027
|
T | C | 53 | a0001c0001t0006g0009a0001c0001t0006g0020a0001c0001t0006g0047others(50): Show | 61 | HG00735.hp2 HG01069.hp1 HG01069.hp2 others(58): Show |
intron_variant | MODIFIER | c.975+2924T>C | MFN1 | ENSG00000171109.19 | transcript | ENST00000471841.6 | protein_coding | 9/17 | chr3 | 179371027 | ||||||
chr3:179371355
|
G | GA | 235 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0018others(232): Show | 283 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(280): Show |
intron_variant | MODIFIER | c.975+3263dupA | MFN1 | ENSG00000171109.19 | transcript | ENST00000471841.6 | protein_coding | 9/17 | INFO_REALIGN_3_PRIME | chr3 | 179371355 | |||||
chr3:179371641
|
A | G | 6 | a0001c0002t0004g0282a0001c0002t0004g0285a0001c0002t0016g0281others(3): Show | 6 | HG03669.hp1 HG03688.hp2 HG03704.hp1 others(3): Show |
intron_variant | MODIFIER | c.975+3538A>G | MFN1 | ENSG00000171109.19 | transcript | ENST00000471841.6 | protein_coding | 9/17 | chr3 | 179371641 | ||||||
chr3:179371707
|
C | T | 1 | a0001c0001t0001g0280 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.976-3513C>T | MFN1 | ENSG00000171109.19 | transcript | ENST00000471841.6 | protein_coding | 9/17 | chr3 | 179371707 | ||||||
chr3:179371823
|
A | C | 1 | a0001c0002t0016g0286 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.976-3397A>C | MFN1 | ENSG00000171109.19 | transcript | ENST00000471841.6 | protein_coding | 9/17 | chr3 | 179371823 | ||||||
chr3:179371997
|
G | A | 1 | a0001c0001t0032g0229 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.976-3223G>A | MFN1 | ENSG00000171109.19 | transcript | ENST00000471841.6 | protein_coding | 9/17 | chr3 | 179371997 | ||||||
chr3:179372015
|
A | T | 67 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0018others(64): Show | 83 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(80): Show |
intron_variant | MODIFIER | c.976-3205A>T | MFN1 | ENSG00000171109.19 | transcript | ENST00000471841.6 | protein_coding | 9/17 | chr3 | 179372015 | ||||||
chr3:179372036
|
A | G | 53 | a0001c0001t0006g0009a0001c0001t0006g0020a0001c0001t0006g0047others(50): Show | 61 | HG00735.hp2 HG01069.hp1 HG01069.hp2 others(58): Show |
intron_variant | MODIFIER | c.976-3184A>G | MFN1 | ENSG00000171109.19 | transcript | ENST00000471841.6 | protein_coding | 9/17 | chr3 | 179372036 | ||||||
chr3:179372053
|
T | TTATTATA | 10 | a0001c0001t0009g0024a0001c0001t0009g0025a0001c0001t0009g0057others(7): Show | 11 | HG02257.hp2 HG02572.hp2 HG02630.hp2 others(8): Show |
intron_variant | MODIFIER | c.976-3150_976-3144d others(9): Show |
MFN1 | ENSG00000171109.19 | transcript | ENST00000471841.6 | protein_coding | 9/17 | INFO_REALIGN_3_PRIME | chr3 | 179372053 | |||||
chr3:179372053
|
T | TTATTATA others(7): Show |
1 | a0001c0001t0009g0289 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.976-3157_976-3144d others(16): Show |
MFN1 | ENSG00000171109.19 | transcript | ENST00000471841.6 | protein_coding | 9/17 | INFO_REALIGN_3_PRIME | chr3 | 179372053 | |||||
chr3:179372084
|
T | C | 78 | a0001c0001t0002g0003a0001c0001t0002g0005a0001c0001t0002g0006others(75): Show | 91 | HG00140.hp2 HG00280.hp1 HG00408.hp2 others(88): Show |
intron_variant | MODIFIER | c.976-3136T>C | MFN1 | ENSG00000171109.19 | transcript | ENST00000471841.6 | protein_coding | 9/17 | chr3 | 179372084 | ||||||
chr3:179372140
|
GGA | G | 8 | a0001c0002t0004g0282a0001c0002t0004g0285a0001c0002t0016g0281others(5): Show | 8 | HG02559.hp2 HG03669.hp1 HG03688.hp2 others(5): Show |
intron_variant | MODIFIER | c.976-3072_976-3071d others(4): Show |
MFN1 | ENSG00000171109.19 | transcript | ENST00000471841.6 | protein_coding | 9/17 | INFO_REALIGN_3_PRIME | chr3 | 179372140 | |||||
chr3:179372289
|
A | G | 1 | a0001c0001t0005g0098 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.976-2931A>G | MFN1 | ENSG00000171109.19 | transcript | ENST00000471841.6 | protein_coding | 9/17 | chr3 | 179372289 | ||||||
chr3:179372297
|
T | G | 1 | a0001c0001t0036g0210 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.976-2923T>G | MFN1 | ENSG00000171109.19 | transcript | ENST00000471841.6 | protein_coding | 9/17 | chr3 | 179372297 | ||||||
chr3:179372303
|
T | C | 6 | a0001c0002t0004g0282a0001c0002t0004g0285a0001c0002t0016g0281others(3): Show | 6 | HG03669.hp1 HG03688.hp2 HG03704.hp1 others(3): Show |
intron_variant | MODIFIER | c.976-2917T>C | MFN1 | ENSG00000171109.19 | transcript | ENST00000471841.6 | protein_coding | 9/17 | chr3 | 179372303 | ||||||
chr3:179372358
|
A | G | 1 | a0001c0001t0002g0228 | 1 | NA19082.hp2 | intron_variant | MODIFIER | c.976-2862A>G | MFN1 | ENSG00000171109.19 | transcript | ENST00000471841.6 | protein_coding | 9/17 | chr3 | 179372358 | ||||||
chr3:179372369
|
T | A | 53 | a0001c0001t0006g0009a0001c0001t0006g0020a0001c0001t0006g0047others(50): Show | 61 | HG00735.hp2 HG01069.hp1 HG01069.hp2 others(58): Show |
intron_variant | MODIFIER | c.976-2851T>A | MFN1 | ENSG00000171109.19 | transcript | ENST00000471841.6 | protein_coding | 9/17 | chr3 | 179372369 | ||||||
chr3:179372479
|
T | C | 1 | a0001c0001t0002g0211 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.976-2741T>C | MFN1 | ENSG00000171109.19 | transcript | ENST00000471841.6 | protein_coding | 9/17 | chr3 | 179372479 | ||||||
chr3:179372608
|
C | T | 58 | a0001c0001t0001g0008a0001c0001t0001g0018a0001c0001t0001g0019others(55): Show | 69 | HG00408.hp1 HG00423.hp2 HG00597.hp1 others(66): Show |
intron_variant | MODIFIER | c.976-2612C>T | MFN1 | ENSG00000171109.19 | transcript | ENST00000471841.6 | protein_coding | 9/17 | chr3 | 179372608 | ||||||
chr3:179372788
|
G | T | 1 | a0001c0001t0014g0072 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.976-2432G>T | MFN1 | ENSG00000171109.19 | transcript | ENST00000471841.6 | protein_coding | 9/17 | chr3 | 179372788 | ||||||
chr3:179372984
|
G | A | 169 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0018others(166): Show | 205 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(202): Show |
intron_variant | MODIFIER | c.976-2236G>A | MFN1 | ENSG00000171109.19 | transcript | ENST00000471841.6 | protein_coding | 9/17 | chr3 | 179372984 | ||||||
chr3:179373188
|
T | C | 1 | a0001c0002t0016g0283 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.976-2032T>C | MFN1 | ENSG00000171109.19 | transcript | ENST00000471841.6 | protein_coding | 9/17 | chr3 | 179373188 | ||||||
chr3:179373209
|
A | G | 5 | a0001c0001t0019g0054a0001c0001t0019g0105a0001c0001t0019g0106others(2): Show | 5 | HG02647.hp1 HG02896.hp1 HG02965.hp1 others(2): Show |
intron_variant | MODIFIER | c.976-2011A>G | MFN1 | ENSG00000171109.19 | transcript | ENST00000471841.6 | protein_coding | 9/17 | chr3 | 179373209 | ||||||
chr3:179373254
|
GTCTT | G | 67 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0018others(64): Show | 83 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(80): Show |
intron_variant | MODIFIER | c.976-1962_976-1959d others(6): Show |
MFN1 | ENSG00000171109.19 | transcript | ENST00000471841.6 | protein_coding | 9/17 | INFO_REALIGN_3_PRIME | chr3 | 179373254 | |||||
chr3:179373375
|
T | G | 10 | a0001c0001t0002g0003a0001c0001t0002g0036a0001c0001t0002g0175others(7): Show | 14 | HG00609.hp2 HG02015.hp2 HG02071.hp2 others(11): Show |
intron_variant | MODIFIER | c.976-1845T>G | MFN1 | ENSG00000171109.19 | transcript | ENST00000471841.6 | protein_coding | 9/17 | chr3 | 179373375 | ||||||
chr3:179373485
|
G | A | 8 | a0001c0002t0004g0282a0001c0002t0004g0285a0001c0002t0016g0281others(5): Show | 8 | HG02559.hp2 HG03669.hp1 HG03688.hp2 others(5): Show |
intron_variant | MODIFIER | c.976-1735G>A | MFN1 | ENSG00000171109.19 | transcript | ENST00000471841.6 | protein_coding | 9/17 | chr3 | 179373485 | ||||||
chr3:179373735
|
G | A | 1 | a0001c0001t0003g0117 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.976-1485G>A | MFN1 | ENSG00000171109.19 | transcript | ENST00000471841.6 | protein_coding | 9/17 | chr3 | 179373735 | ||||||
chr3:179373964
|
C | T | 1 | a0001c0009t0039g0225 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.976-1256C>T | MFN1 | ENSG00000171109.19 | transcript | ENST00000471841.6 | protein_coding | 9/17 | chr3 | 179373964 | ||||||
chr3:179374068
|
T | C | 49 | a0001c0001t0001g0002a0001c0001t0001g0010a0001c0001t0001g0011others(46): Show | 62 | HG00438.hp2 HG00544.hp2 HG00597.hp2 others(59): Show |
intron_variant | MODIFIER | c.976-1152T>C | MFN1 | ENSG00000171109.19 | transcript | ENST00000471841.6 | protein_coding | 9/17 | chr3 | 179374068 | ||||||
chr3:179374070
|
A | G | 1 | a0001c0001t0005g0098 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.976-1150A>G | MFN1 | ENSG00000171109.19 | transcript | ENST00000471841.6 | protein_coding | 9/17 | chr3 | 179374070 | ||||||
chr3:179374266
|
G | A | 1 | a0001c0001t0003g0253 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.976-954G>A | MFN1 | ENSG00000171109.19 | transcript | ENST00000471841.6 | protein_coding | 9/17 | chr3 | 179374266 | ||||||
chr3:179374301
|
A | AAATATAT others(26): Show |
50 | a0001c0001t0002g0003a0001c0001t0002g0005a0001c0001t0002g0006others(47): Show | 62 | HG00280.hp1 HG00423.hp1 HG00544.hp1 others(59): Show |
intron_variant | MODIFIER | c.976-840_976-808dup others(33): Show |
MFN1 | ENSG00000171109.19 | transcript | ENST00000471841.6 | protein_coding | 9/17 | INFO_REALIGN_3_PRIME | chr3 | 179374301 | |||||
chr3:179374301
|
A | AAATATAT others(59): Show |
24 | a0001c0001t0002g0038a0001c0001t0002g0157a0001c0001t0002g0158others(21): Show | 25 | HG00408.hp2 HG00738.hp1 HG01243.hp2 others(22): Show |
intron_variant | MODIFIER | c.976-873_976-808dup others(66): Show |
MFN1 | ENSG00000171109.19 | transcript | ENST00000471841.6 | protein_coding | 9/17 | INFO_REALIGN_3_PRIME | chr3 | 179374301 | |||||
chr3:179374301
|
AAATATAT others(26): Show |
A | 210 | a0001c0001t0001g0002a0001c0001t0001g0007a0001c0001t0001g0008others(207): Show | 259 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(256): Show |
intron_variant | MODIFIER | c.976-840_976-808del others(33): Show |
MFN1 | ENSG00000171109.19 | transcript | ENST00000471841.6 | protein_coding | 9/17 | INFO_REALIGN_3_PRIME | chr3 | 179374301 | |||||
chr3:179374301
|
AAATATAT others(59): Show |
A | 1 | a0001c0001t0007g0140 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.976-873_976-808del others(66): Show |
MFN1 | ENSG00000171109.19 | transcript | ENST00000471841.6 | protein_coding | 9/17 | INFO_REALIGN_3_PRIME | chr3 | 179374301 | |||||
chr3:179374302
|
A | AATATATA others(26): Show |
1 | a0001c0001t0002g0169 | 1 | NA18985.hp2 | intron_variant | MODIFIER | c.976-886_976-885ins others(33): Show |
MFN1 | ENSG00000171109.19 | transcript | ENST00000471841.6 | protein_coding | 9/17 | INFO_REALIGN_3_PRIME | chr3 | 179374302 | |||||
chr3:179374335
|
A | AATATATA others(26): Show |
2 | a0001c0001t0002g0181a0001c0001t0002g0182 | 2 | HG00140.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.976-853_976-852ins others(33): Show |
MFN1 | ENSG00000171109.19 | transcript | ENST00000471841.6 | protein_coding | 9/17 | INFO_REALIGN_3_PRIME | chr3 | 179374335 | |||||
chr3:179374339
|
TATATATA others(35): Show |
T | 1 | a0001c0005t0027g0288 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.976-864_976-823del others(42): Show |
MFN1 | ENSG00000171109.19 | transcript | ENST00000471841.6 | protein_coding | 9/17 | INFO_REALIGN_3_PRIME | chr3 | 179374339 | |||||
chr3:179374346
|
A | T | 1 | a0001c0001t0014g0074 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.976-874A>T | MFN1 | ENSG00000171109.19 | transcript | ENST00000471841.6 | protein_coding | 9/17 | chr3 | 179374346 | ||||||
chr3:179374368
|
A | AATATATA others(28): Show |
1 | a0001c0001t0011g0187 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.976-839_976-805dup others(35): Show |
MFN1 | ENSG00000171109.19 | transcript | ENST00000471841.6 | protein_coding | 9/17 | INFO_REALIGN_3_PRIME | chr3 | 179374368 | |||||
chr3:179374368
|
AATATATA others(28): Show |
A | 7 | a0001c0002t0004g0282a0001c0002t0004g0285a0001c0002t0016g0281others(4): Show | 7 | HG02559.hp2 HG03669.hp1 HG03688.hp2 others(4): Show |
intron_variant | MODIFIER | c.976-839_976-805del others(35): Show |
MFN1 | ENSG00000171109.19 | transcript | ENST00000471841.6 | protein_coding | 9/17 | INFO_REALIGN_3_PRIME | chr3 | 179374368 | |||||
chr3:179374370
|
TATATATA others(24): Show |
T | 8 | a0001c0001t0001g0004a0001c0001t0001g0138a0001c0001t0001g0141others(5): Show | 11 | HG01255.hp1 HG02145.hp1 HG02258.hp1 others(8): Show |
intron_variant | MODIFIER | c.976-840_976-810del others(31): Show |
MFN1 | ENSG00000171109.19 | transcript | ENST00000471841.6 | protein_coding | 9/17 | INFO_REALIGN_3_PRIME | chr3 | 179374370 | |||||
chr3:179374372
|
TATATATA others(2): Show |
T | 3 | a0001c0001t0020g0101a0001c0001t0020g0102a0001c0001t0020g0216 | 3 | HG01433.hp1 HG02280.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.976-831_976-823del others(9): Show |
MFN1 | ENSG00000171109.19 | transcript | ENST00000471841.6 | protein_coding | 9/17 | INFO_REALIGN_3_PRIME | chr3 | 179374372 | |||||
chr3:179374379
|
A | T | 1 | a0001c0001t0038g0294 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.976-841A>T | MFN1 | ENSG00000171109.19 | transcript | ENST00000471841.6 | protein_coding | 9/17 | chr3 | 179374379 | ||||||
chr3:179374452
|
A | ATGT | 197 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0018others(194): Show | 230 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(227): Show |
intron_variant | MODIFIER | c.976-767_976-765dup others(3): Show |
MFN1 | ENSG00000171109.19 | transcript | ENST00000471841.6 | protein_coding | 9/17 | INFO_REALIGN_3_PRIME | chr3 | 179374452 | |||||
chr3:179374704
|
C | T | 10 | a0001c0001t0001g0004a0001c0001t0001g0077a0001c0001t0001g0078others(7): Show | 13 | HG01081.hp2 HG01106.hp1 HG01255.hp1 others(10): Show |
intron_variant | MODIFIER | c.976-516C>T | MFN1 | ENSG00000171109.19 | transcript | ENST00000471841.6 | protein_coding | 9/17 | chr3 | 179374704 | ||||||
chr3:179374980
|
A | C | 1 | a0001c0001t0014g0071 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.976-240A>C | MFN1 | ENSG00000171109.19 | transcript | ENST00000471841.6 | protein_coding | 9/17 | chr3 | 179374980 | ||||||
chr3:179375026
|
T | C | 22 | a0001c0001t0004g0001a0001c0001t0004g0026a0001c0001t0004g0069others(19): Show | 32 | HG00140.hp1 HG00323.hp1 HG00438.hp1 others(29): Show |
intron_variant | MODIFIER | c.976-194T>C | MFN1 | ENSG00000171109.19 | transcript | ENST00000471841.6 | protein_coding | 9/17 | chr3 | 179375026 | ||||||
chr3:179375201
|
C | T | 247 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0018others(244): Show | 296 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(293): Show |
intron_variant | MODIFIER | c.976-19C>T | MFN1 | ENSG00000171109.19 | transcript | ENST00000471841.6 | protein_coding | 9/17 | chr3 | 179375201 | ||||||
chr3:179375542
|
A | G | 6 | a0001c0001t0015g0021a0001c0001t0015g0299a0001c0001t0015g0300others(3): Show | 7 | HG01167.hp2 HG01169.hp1 HG02109.hp1 others(4): Show |
intron_variant | MODIFIER | c.1097+201A>G | MFN1 | ENSG00000171109.19 | transcript | ENST00000471841.6 | protein_coding | 10/17 | chr3 | 179375542 | ||||||
chr3:179375828
|
A | G | 48 | a0001c0001t0006g0009a0001c0001t0006g0020a0001c0001t0006g0047others(45): Show | 56 | HG00735.hp2 HG01069.hp1 HG01069.hp2 others(53): Show |
intron_variant | MODIFIER | c.1097+487A>G | MFN1 | ENSG00000171109.19 | transcript | ENST00000471841.6 | protein_coding | 10/17 | chr3 | 179375828 | ||||||
chr3:179375852
|
G | A | 1 | a0001c0001t0002g0164 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.1097+511G>A | MFN1 | ENSG00000171109.19 | transcript | ENST00000471841.6 | protein_coding | 10/17 | chr3 | 179375852 | ||||||
chr3:179375914
|
A | G | 1 | a0001c0001t0011g0163 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.1097+573A>G | MFN1 | ENSG00000171109.19 | transcript | ENST00000471841.6 | protein_coding | 10/17 | chr3 | 179375914 | ||||||
chr3:179375968
|
G | A | 1 | a0001c0001t0007g0248 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.1097+627G>A | MFN1 | ENSG00000171109.19 | transcript | ENST00000471841.6 | protein_coding | 10/17 | chr3 | 179375968 | ||||||
chr3:179376010
|
G | A | 247 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0018others(244): Show | 296 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(293): Show |
intron_variant | MODIFIER | c.1097+669G>A | MFN1 | ENSG00000171109.19 | transcript | ENST00000471841.6 | protein_coding | 10/17 | chr3 | 179376010 | ||||||
chr3:179376048
|
CAT | C | 7 | a0001c0001t0001g0018a0001c0001t0001g0045a0001c0001t0001g0230others(4): Show | 9 | HG02486.hp1 HG02622.hp2 HG02630.hp1 others(6): Show |
intron_variant | MODIFIER | c.1097+709_1097+710d others(4): Show |
MFN1 | ENSG00000171109.19 | transcript | ENST00000471841.6 | protein_coding | 10/17 | INFO_REALIGN_3_PRIME | chr3 | 179376048 | |||||
chr3:179376598
|
C | G | 13 | a0001c0001t0004g0001a0001c0001t0004g0026a0001c0001t0004g0079others(10): Show | 23 | HG00140.hp1 HG00323.hp1 HG00438.hp1 others(20): Show |
intron_variant | MODIFIER | c.1098-444C>G | MFN1 | ENSG00000171109.19 | transcript | ENST00000471841.6 | protein_coding | 10/17 | chr3 | 179376598 | ||||||
chr3:179376736
|
C | T | 24 | a0001c0001t0006g0009a0001c0001t0006g0020a0001c0001t0006g0047others(21): Show | 30 | HG01069.hp2 HG01071.hp1 HG01167.hp2 others(27): Show |
intron_variant | MODIFIER | c.1098-306C>T | MFN1 | ENSG00000171109.19 | transcript | ENST00000471841.6 | protein_coding | 10/17 | chr3 | 179376736 | ||||||
chr3:179376782
|
A | G | 1 | a0001c0009t0039g0225 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.1098-260A>G | MFN1 | ENSG00000171109.19 | transcript | ENST00000471841.6 | protein_coding | 10/17 | chr3 | 179376782 | ||||||
chr3:179377023
|
A | G | 17 | a0001c0001t0006g0009a0001c0001t0006g0020a0001c0001t0006g0047others(14): Show | 22 | HG01069.hp2 HG01071.hp1 HG01175.hp1 others(19): Show |
intron_variant | MODIFIER | c.1098-19A>G | MFN1 | ENSG00000171109.19 | transcript | ENST00000471841.6 | protein_coding | 10/17 | chr3 | 179377023 | ||||||
chr3:179377276
|
A | G | 1 | a0001c0001t0009g0289 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.1225-68A>G | MFN1 | ENSG00000171109.19 | transcript | ENST00000471841.6 | protein_coding | 11/17 | chr3 | 179377276 | ||||||
chr3:179377301
|
A | G | 1 | a0001c0001t0001g0119 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.1225-43A>G | MFN1 | ENSG00000171109.19 | transcript | ENST00000471841.6 | protein_coding | 11/17 | chr3 | 179377301 | ||||||
chr3:179377491
|
A | C | 11 | a0001c0001t0009g0024a0001c0001t0009g0025a0001c0001t0009g0057others(8): Show | 12 | HG02257.hp2 HG02572.hp2 HG02630.hp2 others(9): Show |
intron_variant | MODIFIER | c.1329+43A>C | MFN1 | ENSG00000171109.19 | transcript | ENST00000471841.6 | protein_coding | 12/17 | chr3 | 179377491 | ||||||
chr3:179377577
|
G | A | 1 | a0003c0006t0003g0245 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.1329+129G>A | MFN1 | ENSG00000171109.19 | transcript | ENST00000471841.6 | protein_coding | 12/17 | chr3 | 179377577 | ||||||
chr3:179377622
|
A | G | 1 | a0001c0009t0039g0225 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.1329+174A>G | MFN1 | ENSG00000171109.19 | transcript | ENST00000471841.6 | protein_coding | 12/17 | chr3 | 179377622 | ||||||
chr3:179377653
|
A | C | 1 | a0001c0001t0010g0084 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.1329+205A>C | MFN1 | ENSG00000171109.19 | transcript | ENST00000471841.6 | protein_coding | 12/17 | chr3 | 179377653 | ||||||
chr3:179377679
|
A | G | 5 | a0001c0001t0020g0101a0001c0001t0020g0102a0001c0001t0020g0216others(2): Show | 5 | HG01433.hp1 HG02257.hp1 HG02280.hp1 others(2): Show |
intron_variant | MODIFIER | c.1329+231A>G | MFN1 | ENSG00000171109.19 | transcript | ENST00000471841.6 | protein_coding | 12/17 | chr3 | 179377679 | ||||||
chr3:179377700
|
G | A | 5 | a0001c0001t0019g0054a0001c0001t0019g0105a0001c0001t0019g0106others(2): Show | 5 | HG02647.hp1 HG02896.hp1 HG02965.hp1 others(2): Show |
intron_variant | MODIFIER | c.1329+252G>A | MFN1 | ENSG00000171109.19 | transcript | ENST00000471841.6 | protein_coding | 12/17 | chr3 | 179377700 | ||||||
chr3:179377731
|
C | T | 17 | a0001c0001t0006g0009a0001c0001t0006g0020a0001c0001t0006g0047others(14): Show | 22 | HG01069.hp2 HG01071.hp1 HG01175.hp1 others(19): Show |
intron_variant | MODIFIER | c.1329+283C>T | MFN1 | ENSG00000171109.19 | transcript | ENST00000471841.6 | protein_coding | 12/17 | chr3 | 179377731 | ||||||
chr3:179377732
|
G | A | 6 | a0001c0002t0004g0282a0001c0002t0004g0285a0001c0002t0016g0281others(3): Show | 6 | HG03669.hp1 HG03688.hp2 HG03704.hp1 others(3): Show |
intron_variant | MODIFIER | c.1329+284G>A | MFN1 | ENSG00000171109.19 | transcript | ENST00000471841.6 | protein_coding | 12/17 | chr3 | 179377732 | ||||||
chr3:179377780
|
T | C | 1 | a0001c0009t0039g0225 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.1329+332T>C | MFN1 | ENSG00000171109.19 | transcript | ENST00000471841.6 | protein_coding | 12/17 | chr3 | 179377780 | ||||||
chr3:179377802
|
C | T | 40 | a0001c0001t0004g0001a0001c0001t0004g0026a0001c0001t0004g0069others(37): Show | 52 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(49): Show |
intron_variant | MODIFIER | c.1329+354C>T | MFN1 | ENSG00000171109.19 | transcript | ENST00000471841.6 | protein_coding | 12/17 | chr3 | 179377802 | ||||||
chr3:179377835
|
C | T | 1 | a0001c0001t0001g0116 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.1329+387C>T | MFN1 | ENSG00000171109.19 | transcript | ENST00000471841.6 | protein_coding | 12/17 | chr3 | 179377835 | ||||||
chr3:179377884
|
G | A | 53 | a0001c0001t0006g0009a0001c0001t0006g0020a0001c0001t0006g0047others(50): Show | 61 | HG00735.hp2 HG01069.hp1 HG01069.hp2 others(58): Show |
intron_variant | MODIFIER | c.1329+436G>A | MFN1 | ENSG00000171109.19 | transcript | ENST00000471841.6 | protein_coding | 12/17 | chr3 | 179377884 | ||||||
chr3:179377922
|
C | T | 2 | a0001c0001t0001g0030a0001c0001t0001g0124 | 3 | HG00544.hp2 NA18951.hp2 NA18985.hp1 |
intron_variant | MODIFIER | c.1330-419C>T | MFN1 | ENSG00000171109.19 | transcript | ENST00000471841.6 | protein_coding | 12/17 | chr3 | 179377922 | ||||||
chr3:179377933
|
G | A | 1 | a0001c0001t0050g0233 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.1330-408G>A | MFN1 | ENSG00000171109.19 | transcript | ENST00000471841.6 | protein_coding | 12/17 | chr3 | 179377933 | ||||||
chr3:179378056
|
A | G | 1 | a0001c0001t0006g0048 | 2 | HG02109.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.1330-285A>G | MFN1 | ENSG00000171109.19 | transcript | ENST00000471841.6 | protein_coding | 12/17 | chr3 | 179378056 | ||||||
chr3:179378132
|
G | A | 67 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0018others(64): Show | 83 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(80): Show |
intron_variant | MODIFIER | c.1330-209G>A | MFN1 | ENSG00000171109.19 | transcript | ENST00000471841.6 | protein_coding | 12/17 | chr3 | 179378132 | ||||||
chr3:179378218
|
C | CA | 156 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0018others(153): Show | 191 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(188): Show |
intron_variant | MODIFIER | c.1330-108dupA | MFN1 | ENSG00000171109.19 | transcript | ENST00000471841.6 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr3 | 179378218 | |||||
chr3:179378218
|
C | CAA | 15 | a0001c0001t0001g0247a0001c0001t0007g0259a0001c0001t0015g0021others(12): Show | 16 | HG01167.hp2 HG01169.hp1 HG01433.hp1 others(13): Show |
intron_variant | MODIFIER | c.1330-109_1330-108d others(4): Show |
MFN1 | ENSG00000171109.19 | transcript | ENST00000471841.6 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr3 | 179378218 | |||||
chr3:179378218
|
CA | C | 8 | a0001c0001t0001g0034a0001c0001t0001g0107a0001c0001t0001g0111others(5): Show | 9 | HG00438.hp2 HG02132.hp2 HG02155.hp2 others(6): Show |
intron_variant | MODIFIER | c.1330-108delA | MFN1 | ENSG00000171109.19 | transcript | ENST00000471841.6 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr3 | 179378218 | |||||
chr3:179378471
|
C | A | 2 | a0001c0001t0023g0303a0001c0001t0023g0304 | 2 | HG02257.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.1432+28C>A | MFN1 | ENSG00000171109.19 | transcript | ENST00000471841.6 | protein_coding | 13/17 | chr3 | 179378471 | ||||||
chr3:179379006
|
AC | A | 6 | a0001c0001t0015g0021a0001c0001t0015g0299a0001c0001t0015g0300others(3): Show | 7 | HG01167.hp2 HG01169.hp1 HG02109.hp1 others(4): Show |
intron_variant | MODIFIER | c.1662+193delC | MFN1 | ENSG00000171109.19 | transcript | ENST00000471841.6 | protein_coding | 14/17 | chr3 | 179379006 | ||||||
chr3:179379141
|
G | A | 5 | a0001c0001t0019g0054a0001c0001t0019g0105a0001c0001t0019g0106others(2): Show | 5 | HG02647.hp1 HG02896.hp1 HG02965.hp1 others(2): Show |
intron_variant | MODIFIER | c.1662+327G>A | MFN1 | ENSG00000171109.19 | transcript | ENST00000471841.6 | protein_coding | 14/17 | chr3 | 179379141 | ||||||
chr3:179379146
|
A | G | 2 | a0001c0001t0041g0032a0001c0001t0042g0032 | 2 | HG02258.hp1 HG02809.hp1 |
intron_variant | MODIFIER | c.1662+332A>G | MFN1 | ENSG00000171109.19 | transcript | ENST00000471841.6 | protein_coding | 14/17 | chr3 | 179379146 | ||||||
chr3:179379150
|
CTT | C | 40 | a0001c0001t0004g0001a0001c0001t0004g0026a0001c0001t0004g0069others(37): Show | 52 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(49): Show |
intron_variant | MODIFIER | c.1662+339_1662+340d others(4): Show |
MFN1 | ENSG00000171109.19 | transcript | ENST00000471841.6 | protein_coding | 14/17 | INFO_REALIGN_3_PRIME | chr3 | 179379150 | |||||
chr3:179379198
|
G | A | 9 | a0001c0001t0004g0069a0001c0001t0004g0089a0001c0001t0004g0091others(6): Show | 9 | HG01192.hp1 HG01515.hp2 HG02602.hp2 others(6): Show |
intron_variant | MODIFIER | c.1662+384G>A | MFN1 | ENSG00000171109.19 | transcript | ENST00000471841.6 | protein_coding | 14/17 | chr3 | 179379198 | ||||||
chr3:179379209
|
G | T | 48 | a0001c0001t0006g0009a0001c0001t0006g0020a0001c0001t0006g0047others(45): Show | 56 | HG00735.hp2 HG01069.hp1 HG01069.hp2 others(53): Show |
intron_variant | MODIFIER | c.1662+395G>T | MFN1 | ENSG00000171109.19 | transcript | ENST00000471841.6 | protein_coding | 14/17 | chr3 | 179379209 | ||||||
chr3:179379246
|
C | T | 1 | a0001c0001t0001g0112 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.1662+432C>T | MFN1 | ENSG00000171109.19 | transcript | ENST00000471841.6 | protein_coding | 14/17 | chr3 | 179379246 | ||||||
chr3:179379345
|
A | T | 3 | a0001c0001t0002g0005a0001c0001t0002g0168a0001c0001t0005g0192 | 7 | NA18947.hp1 NA18998.hp1 NA19005.hp2 others(4): Show |
intron_variant | MODIFIER | c.1662+531A>T | MFN1 | ENSG00000171109.19 | transcript | ENST00000471841.6 | protein_coding | 14/17 | chr3 | 179379345 | ||||||
chr3:179379346
|
A | T | 207 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0018others(204): Show | 244 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(241): Show |
intron_variant | MODIFIER | c.1662+532A>T | MFN1 | ENSG00000171109.19 | transcript | ENST00000471841.6 | protein_coding | 14/17 | chr3 | 179379346 | ||||||
chr3:179379535
|
G | T | 2 | a0001c0001t0001g0016a0001c0001t0001g0152 | 4 | HG02293.hp2 HG03669.hp2 HG03927.hp1 others(1): Show |
intron_variant | MODIFIER | c.1662+721G>T | MFN1 | ENSG00000171109.19 | transcript | ENST00000471841.6 | protein_coding | 14/17 | chr3 | 179379535 | ||||||
chr3:179379744
|
A | C | 24 | a0001c0001t0009g0024a0001c0001t0009g0025a0001c0001t0009g0057others(21): Show | 26 | HG00735.hp2 HG01069.hp1 HG01167.hp1 others(23): Show |
intron_variant | MODIFIER | c.1662+930A>C | MFN1 | ENSG00000171109.19 | transcript | ENST00000471841.6 | protein_coding | 14/17 | chr3 | 179379744 | ||||||
chr3:179379765
|
T | C | 3 | a0001c0001t0011g0154a0001c0001t0011g0186a0001c0001t0028g0185 | 3 | HG00280.hp1 HG00544.hp1 NA19084.hp1 |
intron_variant | MODIFIER | c.1662+951T>C | MFN1 | ENSG00000171109.19 | transcript | ENST00000471841.6 | protein_coding | 14/17 | chr3 | 179379765 | ||||||
chr3:179379922
|
A | T | 1 | a0001c0001t0001g0231 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.1662+1108A>T | MFN1 | ENSG00000171109.19 | transcript | ENST00000471841.6 | protein_coding | 14/17 | chr3 | 179379922 | ||||||
chr3:179380062
|
C | T | 6 | a0001c0001t0018g0022a0001c0001t0018g0050a0001c0001t0018g0052others(3): Show | 7 | HG01069.hp1 HG01167.hp1 HG01884.hp1 others(4): Show |
intron_variant | MODIFIER | c.1662+1248C>T | MFN1 | ENSG00000171109.19 | transcript | ENST00000471841.6 | protein_coding | 14/17 | chr3 | 179380062 | ||||||
chr3:179380084
|
A | G | 2 | a0001c0005t0027g0287a0001c0005t0027g0288 | 2 | HG02559.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.1662+1270A>G | MFN1 | ENSG00000171109.19 | transcript | ENST00000471841.6 | protein_coding | 14/17 | chr3 | 179380084 | ||||||
chr3:179380269
|
T | A | 1 | a0001c0001t0001g0238 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.1662+1455T>A | MFN1 | ENSG00000171109.19 | transcript | ENST00000471841.6 | protein_coding | 14/17 | chr3 | 179380269 | ||||||
chr3:179380291
|
A | G | 4 | a0001c0001t0003g0133a0001c0001t0003g0137a0001c0001t0029g0029others(1): Show | 4 | HG01256.hp2 HG01258.hp1 NA18947.hp2 others(1): Show |
intron_variant | MODIFIER | c.1662+1477A>G | MFN1 | ENSG00000171109.19 | transcript | ENST00000471841.6 | protein_coding | 14/17 | chr3 | 179380291 | ||||||
chr3:179380432
|
AT | A | 247 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0018others(244): Show | 296 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(293): Show |
intron_variant | MODIFIER | c.1662+1626delT | MFN1 | ENSG00000171109.19 | transcript | ENST00000471841.6 | protein_coding | 14/17 | INFO_REALIGN_3_PRIME | chr3 | 179380432 | |||||
chr3:179380552
|
C | T | 24 | a0001c0001t0009g0024a0001c0001t0009g0025a0001c0001t0009g0057others(21): Show | 26 | HG00735.hp2 HG01069.hp1 HG01167.hp1 others(23): Show |
intron_variant | MODIFIER | c.1662+1738C>T | MFN1 | ENSG00000171109.19 | transcript | ENST00000471841.6 | protein_coding | 14/17 | chr3 | 179380552 | ||||||
chr3:179380658
|
G | A | 1 | a0001c0001t0003g0272 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1662+1844G>A | MFN1 | ENSG00000171109.19 | transcript | ENST00000471841.6 | protein_coding | 14/17 | chr3 | 179380658 | ||||||
chr3:179380666
|
T | C | 6 | a0001c0001t0018g0022a0001c0001t0018g0050a0001c0001t0018g0052others(3): Show | 7 | HG01069.hp1 HG01167.hp1 HG01884.hp1 others(4): Show |
intron_variant | MODIFIER | c.1662+1852T>C | MFN1 | ENSG00000171109.19 | transcript | ENST00000471841.6 | protein_coding | 14/17 | chr3 | 179380666 | ||||||
chr3:179380669
|
G | A | 1 | a0003c0006t0003g0245 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.1662+1855G>A | MFN1 | ENSG00000171109.19 | transcript | ENST00000471841.6 | protein_coding | 14/17 | chr3 | 179380669 | ||||||
chr3:179380735
|
G | A | 1 | a0001c0001t0002g0223 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.1662+1921G>A | MFN1 | ENSG00000171109.19 | transcript | ENST00000471841.6 | protein_coding | 14/17 | chr3 | 179380735 | ||||||
chr3:179380887
|
C | T | 2 | a0001c0005t0027g0287a0001c0005t0027g0288 | 2 | HG02559.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.1662+2073C>T | MFN1 | ENSG00000171109.19 | transcript | ENST00000471841.6 | protein_coding | 14/17 | chr3 | 179380887 | ||||||
chr3:179380934
|
GTGAGCTC others(2): Show |
G | 67 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0018others(64): Show | 83 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(80): Show |
intron_variant | MODIFIER | c.1662+2122_1662+213 others(13): Show |
MFN1 | ENSG00000171109.19 | transcript | ENST00000471841.6 | protein_coding | 14/17 | INFO_REALIGN_3_PRIME | chr3 | 179380934 | |||||
chr3:179380983
|
G | C | 1 | a0001c0001t0001g0121 | 1 | NA18993.hp1 | intron_variant | MODIFIER | c.1662+2169G>C | MFN1 | ENSG00000171109.19 | transcript | ENST00000471841.6 | protein_coding | 14/17 | chr3 | 179380983 | ||||||
chr3:179381136
|
A | G | 1 | a0005c0010t0032g0208 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.1662+2322A>G | MFN1 | ENSG00000171109.19 | transcript | ENST00000471841.6 | protein_coding | 14/17 | chr3 | 179381136 | ||||||
chr3:179381180
|
G | C | 2 | a0001c0001t0003g0271a0001c0001t0003g0272 | 2 | NA19240.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.1662+2366G>C | MFN1 | ENSG00000171109.19 | transcript | ENST00000471841.6 | protein_coding | 14/17 | chr3 | 179381180 | ||||||
chr3:179381321
|
C | T | 1 | a0001c0002t0016g0286 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.1662+2507C>T | MFN1 | ENSG00000171109.19 | transcript | ENST00000471841.6 | protein_coding | 14/17 | chr3 | 179381321 | ||||||
chr3:179381391
|
C | A | 247 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0018others(244): Show | 296 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(293): Show |
intron_variant | MODIFIER | c.1662+2577C>A | MFN1 | ENSG00000171109.19 | transcript | ENST00000471841.6 | protein_coding | 14/17 | chr3 | 179381391 | ||||||
chr3:179381509
|
G | A | 1 | a0001c0001t0001g0139 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1662+2695G>A | MFN1 | ENSG00000171109.19 | transcript | ENST00000471841.6 | protein_coding | 14/17 | chr3 | 179381509 | ||||||
chr3:179381673
|
GCAACA | G | 4 | a0001c0001t0003g0133a0001c0001t0003g0136a0001c0001t0003g0137others(1): Show | 4 | HG00735.hp1 HG01256.hp2 HG01258.hp1 others(1): Show |
intron_variant | MODIFIER | c.1662+2861_1662+286 others(9): Show |
MFN1 | ENSG00000171109.19 | transcript | ENST00000471841.6 | protein_coding | 14/17 | INFO_REALIGN_3_PRIME | chr3 | 179381673 | |||||
chr3:179381853
|
C | A | 8 | a0001c0002t0004g0282a0001c0002t0004g0285a0001c0002t0016g0281others(5): Show | 8 | HG02559.hp2 HG03669.hp1 HG03688.hp2 others(5): Show |
intron_variant | MODIFIER | c.1662+3039C>A | MFN1 | ENSG00000171109.19 | transcript | ENST00000471841.6 | protein_coding | 14/17 | chr3 | 179381853 | ||||||
chr3:179381960
|
T | C | 8 | a0001c0002t0004g0282a0001c0002t0004g0285a0001c0002t0016g0281others(5): Show | 8 | HG02559.hp2 HG03669.hp1 HG03688.hp2 others(5): Show |
intron_variant | MODIFIER | c.1662+3146T>C | MFN1 | ENSG00000171109.19 | transcript | ENST00000471841.6 | protein_coding | 14/17 | chr3 | 179381960 | ||||||
chr3:179381962
|
G | A | 6 | a0001c0002t0004g0282a0001c0002t0004g0285a0001c0002t0016g0281others(3): Show | 6 | HG03669.hp1 HG03688.hp2 HG03704.hp1 others(3): Show |
intron_variant | MODIFIER | c.1662+3148G>A | MFN1 | ENSG00000171109.19 | transcript | ENST00000471841.6 | protein_coding | 14/17 | chr3 | 179381962 | ||||||
chr3:179381967
|
A | G | 2 | a0001c0001t0017g0039a0001c0001t0032g0229 | 3 | HG01261.hp2 HG02886.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.1662+3153A>G | MFN1 | ENSG00000171109.19 | transcript | ENST00000471841.6 | protein_coding | 14/17 | chr3 | 179381967 | ||||||
chr3:179382072
|
T | A | 1 | a0001c0001t0012g0059 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.1662+3258T>A | MFN1 | ENSG00000171109.19 | transcript | ENST00000471841.6 | protein_coding | 14/17 | chr3 | 179382072 | ||||||
chr3:179382074
|
A | AT | 181 | a0001c0001t0001g0121a0001c0001t0002g0003a0001c0001t0002g0005others(178): Show | 214 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(211): Show |
intron_variant | MODIFIER | c.1662+3269dupT | MFN1 | ENSG00000171109.19 | transcript | ENST00000471841.6 | protein_coding | 14/17 | INFO_REALIGN_3_PRIME | chr3 | 179382074 | |||||
chr3:179382074
|
ATT | A | 67 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0018others(64): Show | 83 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(80): Show |
intron_variant | MODIFIER | c.1662+3268_1662+326 others(6): Show |
MFN1 | ENSG00000171109.19 | transcript | ENST00000471841.6 | protein_coding | 14/17 | INFO_REALIGN_3_PRIME | chr3 | 179382074 | |||||
chr3:179382153
|
T | C | 67 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0018others(64): Show | 83 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(80): Show |
intron_variant | MODIFIER | c.1662+3339T>C | MFN1 | ENSG00000171109.19 | transcript | ENST00000471841.6 | protein_coding | 14/17 | chr3 | 179382153 | ||||||
chr3:179382168
|
C | T | 1 | a0001c0001t0001g0034 | 2 | NA18960.hp2 NA19056.hp2 |
intron_variant | MODIFIER | c.1662+3354C>T | MFN1 | ENSG00000171109.19 | transcript | ENST00000471841.6 | protein_coding | 14/17 | chr3 | 179382168 | ||||||
chr3:179382438
|
A | G | 48 | a0001c0001t0006g0009a0001c0001t0006g0020a0001c0001t0006g0047others(45): Show | 56 | HG00735.hp2 HG01069.hp1 HG01069.hp2 others(53): Show |
intron_variant | MODIFIER | c.1663-3131A>G | MFN1 | ENSG00000171109.19 | transcript | ENST00000471841.6 | protein_coding | 14/17 | chr3 | 179382438 | ||||||
chr3:179382463
|
G | C | 1 | a0001c0001t0002g0194 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.1663-3106G>C | MFN1 | ENSG00000171109.19 | transcript | ENST00000471841.6 | protein_coding | 14/17 | chr3 | 179382463 | ||||||
chr3:179382506
|
A | G | 2 | a0001c0001t0001g0109a0001c0001t0003g0110 | 2 | NA18961.hp2 NA18978.hp1 |
intron_variant | MODIFIER | c.1663-3063A>G | MFN1 | ENSG00000171109.19 | transcript | ENST00000471841.6 | protein_coding | 14/17 | chr3 | 179382506 | ||||||
chr3:179382651
|
T | A | 1 | a0001c0001t0018g0022 | 2 | HG01069.hp1 HG01884.hp1 |
intron_variant | MODIFIER | c.1663-2918T>A | MFN1 | ENSG00000171109.19 | transcript | ENST00000471841.6 | protein_coding | 14/17 | chr3 | 179382651 | ||||||
chr3:179382788
|
A | G | 24 | a0001c0001t0009g0024a0001c0001t0009g0025a0001c0001t0009g0057others(21): Show | 26 | HG00735.hp2 HG01069.hp1 HG01167.hp1 others(23): Show |
intron_variant | MODIFIER | c.1663-2781A>G | MFN1 | ENSG00000171109.19 | transcript | ENST00000471841.6 | protein_coding | 14/17 | chr3 | 179382788 | ||||||
chr3:179382832
|
A | G | 247 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0018others(244): Show | 296 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(293): Show |
intron_variant | MODIFIER | c.1663-2737A>G | MFN1 | ENSG00000171109.19 | transcript | ENST00000471841.6 | protein_coding | 14/17 | chr3 | 179382832 | ||||||
chr3:179382873
|
T | C | 1 | a0005c0010t0032g0208 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.1663-2696T>C | MFN1 | ENSG00000171109.19 | transcript | ENST00000471841.6 | protein_coding | 14/17 | chr3 | 179382873 | ||||||
chr3:179382878
|
A | G | 1 | a0001c0001t0001g0250 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.1663-2691A>G | MFN1 | ENSG00000171109.19 | transcript | ENST00000471841.6 | protein_coding | 14/17 | chr3 | 179382878 | ||||||
chr3:179383043
|
C | T | 1 | a0001c0001t0006g0048 | 2 | HG02109.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.1663-2526C>T | MFN1 | ENSG00000171109.19 | transcript | ENST00000471841.6 | protein_coding | 14/17 | chr3 | 179383043 | ||||||
chr3:179383141
|
C | T | 32 | a0001c0001t0004g0001a0001c0001t0004g0026a0001c0001t0004g0069others(29): Show | 43 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(40): Show |
intron_variant | MODIFIER | c.1663-2428C>T | MFN1 | ENSG00000171109.19 | transcript | ENST00000471841.6 | protein_coding | 14/17 | chr3 | 179383141 | ||||||
chr3:179383286
|
T | C | 8 | a0001c0001t0001g0034a0001c0001t0001g0107a0001c0001t0001g0111others(5): Show | 9 | HG00438.hp2 HG02132.hp2 HG02155.hp2 others(6): Show |
intron_variant | MODIFIER | c.1663-2283T>C | MFN1 | ENSG00000171109.19 | transcript | ENST00000471841.6 | protein_coding | 14/17 | chr3 | 179383286 | ||||||
chr3:179383368
|
C | G | 1 | a0001c0009t0039g0225 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.1663-2201C>G | MFN1 | ENSG00000171109.19 | transcript | ENST00000471841.6 | protein_coding | 14/17 | chr3 | 179383368 | ||||||
chr3:179383379
|
A | C | 3 | a0001c0001t0020g0101a0001c0001t0020g0102a0001c0001t0020g0216 | 3 | HG01433.hp1 HG02280.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.1663-2190A>C | MFN1 | ENSG00000171109.19 | transcript | ENST00000471841.6 | protein_coding | 14/17 | chr3 | 179383379 | ||||||
chr3:179383478
|
G | GT | 5 | a0001c0001t0019g0054a0001c0001t0019g0105a0001c0001t0019g0106others(2): Show | 5 | HG02647.hp1 HG02896.hp1 HG02965.hp1 others(2): Show |
intron_variant | MODIFIER | c.1663-2090dupT | MFN1 | ENSG00000171109.19 | transcript | ENST00000471841.6 | protein_coding | 14/17 | INFO_REALIGN_3_PRIME | chr3 | 179383478 | |||||
chr3:179383503
|
G | A | 67 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0018others(64): Show | 83 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(80): Show |
intron_variant | MODIFIER | c.1663-2066G>A | MFN1 | ENSG00000171109.19 | transcript | ENST00000471841.6 | protein_coding | 14/17 | chr3 | 179383503 | ||||||
chr3:179383637
|
C | T | 1 | a0001c0001t0048g0128 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.1663-1932C>T | MFN1 | ENSG00000171109.19 | transcript | ENST00000471841.6 | protein_coding | 14/17 | chr3 | 179383637 | ||||||
chr3:179383650
|
A | G | 3 | a0001c0001t0020g0101a0001c0001t0020g0102a0001c0001t0020g0216 | 3 | HG01433.hp1 HG02280.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.1663-1919A>G | MFN1 | ENSG00000171109.19 | transcript | ENST00000471841.6 | protein_coding | 14/17 | chr3 | 179383650 | ||||||
chr3:179383963
|
T | C | 7 | a0001c0001t0004g0069a0001c0001t0004g0089a0001c0001t0004g0092others(4): Show | 7 | HG01192.hp1 HG01515.hp2 HG02602.hp2 others(4): Show |
intron_variant | MODIFIER | c.1663-1606T>C | MFN1 | ENSG00000171109.19 | transcript | ENST00000471841.6 | protein_coding | 14/17 | chr3 | 179383963 | ||||||
chr3:179384028
|
G | A | 17 | a0001c0001t0006g0009a0001c0001t0006g0020a0001c0001t0006g0047others(14): Show | 22 | HG01069.hp2 HG01071.hp1 HG01175.hp1 others(19): Show |
intron_variant | MODIFIER | c.1663-1541G>A | MFN1 | ENSG00000171109.19 | transcript | ENST00000471841.6 | protein_coding | 14/17 | chr3 | 179384028 | ||||||
chr3:179384066
|
A | G | 1 | a0001c0001t0007g0140 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.1663-1503A>G | MFN1 | ENSG00000171109.19 | transcript | ENST00000471841.6 | protein_coding | 14/17 | chr3 | 179384066 | ||||||
chr3:179384066
|
A | T | 1 | a0005c0010t0032g0208 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.1663-1503A>T | MFN1 | ENSG00000171109.19 | transcript | ENST00000471841.6 | protein_coding | 14/17 | chr3 | 179384066 | ||||||
chr3:179384067
|
T | C | 1 | a0005c0010t0032g0208 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.1663-1502T>C | MFN1 | ENSG00000171109.19 | transcript | ENST00000471841.6 | protein_coding | 14/17 | chr3 | 179384067 | ||||||
chr3:179384221
|
C | T | 24 | a0001c0001t0009g0024a0001c0001t0009g0025a0001c0001t0009g0057others(21): Show | 26 | HG00735.hp2 HG01069.hp1 HG01167.hp1 others(23): Show |
intron_variant | MODIFIER | c.1663-1348C>T | MFN1 | ENSG00000171109.19 | transcript | ENST00000471841.6 | protein_coding | 14/17 | chr3 | 179384221 | ||||||
chr3:179384246
|
G | A | 1 | a0001c0001t0014g0074 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.1663-1323G>A | MFN1 | ENSG00000171109.19 | transcript | ENST00000471841.6 | protein_coding | 14/17 | chr3 | 179384246 | ||||||
chr3:179384311
|
G | A | 1 | a0001c0001t0036g0210 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.1663-1258G>A | MFN1 | ENSG00000171109.19 | transcript | ENST00000471841.6 | protein_coding | 14/17 | chr3 | 179384311 | ||||||
chr3:179384356
|
A | G | 5 | a0001c0001t0002g0147a0001c0001t0002g0160a0001c0001t0002g0164others(2): Show | 5 | HG00423.hp1 NA18984.hp1 NA18985.hp2 others(2): Show |
intron_variant | MODIFIER | c.1663-1213A>G | MFN1 | ENSG00000171109.19 | transcript | ENST00000471841.6 | protein_coding | 14/17 | chr3 | 179384356 | ||||||
chr3:179384444
|
A | G | 1 | a0001c0009t0039g0225 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.1663-1125A>G | MFN1 | ENSG00000171109.19 | transcript | ENST00000471841.6 | protein_coding | 14/17 | chr3 | 179384444 | ||||||
chr3:179384475
|
T | G | 6 | a0001c0001t0015g0021a0001c0001t0015g0299a0001c0001t0015g0300others(3): Show | 7 | HG01167.hp2 HG01169.hp1 HG02109.hp1 others(4): Show |
intron_variant | MODIFIER | c.1663-1094T>G | MFN1 | ENSG00000171109.19 | transcript | ENST00000471841.6 | protein_coding | 14/17 | chr3 | 179384475 | ||||||
chr3:179384476
|
T | G | 6 | a0001c0001t0015g0021a0001c0001t0015g0299a0001c0001t0015g0300others(3): Show | 7 | HG01167.hp2 HG01169.hp1 HG02109.hp1 others(4): Show |
intron_variant | MODIFIER | c.1663-1093T>G | MFN1 | ENSG00000171109.19 | transcript | ENST00000471841.6 | protein_coding | 14/17 | chr3 | 179384476 | ||||||
chr3:179384477
|
T | A | 6 | a0001c0001t0015g0021a0001c0001t0015g0299a0001c0001t0015g0300others(3): Show | 7 | HG01167.hp2 HG01169.hp1 HG02109.hp1 others(4): Show |
intron_variant | MODIFIER | c.1663-1092T>A | MFN1 | ENSG00000171109.19 | transcript | ENST00000471841.6 | protein_coding | 14/17 | chr3 | 179384477 | ||||||
chr3:179384478
|
ACCTATTT | A | 6 | a0001c0001t0015g0021a0001c0001t0015g0299a0001c0001t0015g0300others(3): Show | 7 | HG01167.hp2 HG01169.hp1 HG02109.hp1 others(4): Show |
intron_variant | MODIFIER | c.1663-1090_1663-108 others(11): Show |
MFN1 | ENSG00000171109.19 | transcript | ENST00000471841.6 | protein_coding | 14/17 | chr3 | 179384478 | ||||||
chr3:179384486
|
T | A | 6 | a0001c0001t0015g0021a0001c0001t0015g0299a0001c0001t0015g0300others(3): Show | 7 | HG01167.hp2 HG01169.hp1 HG02109.hp1 others(4): Show |
intron_variant | MODIFIER | c.1663-1083T>A | MFN1 | ENSG00000171109.19 | transcript | ENST00000471841.6 | protein_coding | 14/17 | chr3 | 179384486 | ||||||
chr3:179384514
|
A | G | 18 | a0001c0001t0009g0024a0001c0001t0009g0025a0001c0001t0009g0057others(15): Show | 19 | HG00735.hp2 HG01433.hp2 HG02055.hp2 others(16): Show |
intron_variant | MODIFIER | c.1663-1055A>G | MFN1 | ENSG00000171109.19 | transcript | ENST00000471841.6 | protein_coding | 14/17 | chr3 | 179384514 | ||||||
chr3:179384600
|
G | A | 24 | a0001c0001t0009g0024a0001c0001t0009g0025a0001c0001t0009g0057others(21): Show | 26 | HG00735.hp2 HG01069.hp1 HG01167.hp1 others(23): Show |
intron_variant | MODIFIER | c.1663-969G>A | MFN1 | ENSG00000171109.19 | transcript | ENST00000471841.6 | protein_coding | 14/17 | chr3 | 179384600 | ||||||
chr3:179384726
|
G | A | 6 | a0001c0001t0018g0022a0001c0001t0018g0050a0001c0001t0018g0052others(3): Show | 7 | HG01069.hp1 HG01167.hp1 HG01884.hp1 others(4): Show |
intron_variant | MODIFIER | c.1663-843G>A | MFN1 | ENSG00000171109.19 | transcript | ENST00000471841.6 | protein_coding | 14/17 | chr3 | 179384726 | ||||||
chr3:179384740
|
G | A | 66 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0018others(63): Show | 82 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(79): Show |
intron_variant | MODIFIER | c.1663-829G>A | MFN1 | ENSG00000171109.19 | transcript | ENST00000471841.6 | protein_coding | 14/17 | chr3 | 179384740 | ||||||
chr3:179384749
|
G | A | 67 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0018others(64): Show | 83 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(80): Show |
intron_variant | MODIFIER | c.1663-820G>A | MFN1 | ENSG00000171109.19 | transcript | ENST00000471841.6 | protein_coding | 14/17 | chr3 | 179384749 | ||||||
chr3:179384838
|
A | G | 1 | a0001c0001t0036g0210 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.1663-731A>G | MFN1 | ENSG00000171109.19 | transcript | ENST00000471841.6 | protein_coding | 14/17 | chr3 | 179384838 | ||||||
chr3:179384900
|
C | CT | 19 | a0001c0001t0001g0111a0001c0001t0001g0121a0001c0001t0001g0131others(16): Show | 19 | HG00438.hp2 HG00735.hp1 HG01175.hp1 others(16): Show |
intron_variant | MODIFIER | c.1663-646dupT | MFN1 | ENSG00000171109.19 | transcript | ENST00000471841.6 | protein_coding | 14/17 | INFO_REALIGN_3_PRIME | chr3 | 179384900 | |||||
chr3:179384900
|
CT | C | 125 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0018others(122): Show | 156 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(153): Show |
intron_variant | MODIFIER | c.1663-646delT | MFN1 | ENSG00000171109.19 | transcript | ENST00000471841.6 | protein_coding | 14/17 | INFO_REALIGN_3_PRIME | chr3 | 179384900 | |||||
chr3:179384900
|
CTT | C | 23 | a0001c0001t0001g0241a0001c0001t0003g0272a0001c0001t0007g0257others(20): Show | 25 | HG01069.hp1 HG01433.hp1 HG01884.hp1 others(22): Show |
intron_variant | MODIFIER | c.1663-647_1663-646d others(4): Show |
MFN1 | ENSG00000171109.19 | transcript | ENST00000471841.6 | protein_coding | 14/17 | INFO_REALIGN_3_PRIME | chr3 | 179384900 | |||||
chr3:179384974
|
C | T | 6 | a0001c0001t0015g0021a0001c0001t0015g0299a0001c0001t0015g0300others(3): Show | 7 | HG01167.hp2 HG01169.hp1 HG02109.hp1 others(4): Show |
intron_variant | MODIFIER | c.1663-595C>T | MFN1 | ENSG00000171109.19 | transcript | ENST00000471841.6 | protein_coding | 14/17 | chr3 | 179384974 | ||||||
chr3:179384985
|
A | G | 6 | a0001c0001t0006g0047a0001c0001t0006g0296a0001c0001t0006g0297others(3): Show | 6 | HG02258.hp2 HG02486.hp2 HG02615.hp2 others(3): Show |
intron_variant | MODIFIER | c.1663-584A>G | MFN1 | ENSG00000171109.19 | transcript | ENST00000471841.6 | protein_coding | 14/17 | chr3 | 179384985 | ||||||
chr3:179385072
|
A | AT | 13 | a0001c0001t0005g0098a0001c0001t0009g0024a0001c0001t0009g0025others(10): Show | 14 | HG02257.hp2 HG02572.hp1 HG02572.hp2 others(11): Show |
intron_variant | MODIFIER | c.1663-485dupT | MFN1 | ENSG00000171109.19 | transcript | ENST00000471841.6 | protein_coding | 14/17 | INFO_REALIGN_3_PRIME | chr3 | 179385072 | |||||
chr3:179385204
|
C | T | 1 | a0001c0001t0002g0221 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.1663-365C>T | MFN1 | ENSG00000171109.19 | transcript | ENST00000471841.6 | protein_coding | 14/17 | chr3 | 179385204 | ||||||
chr3:179385205
|
G | A | 19 | a0001c0001t0006g0009a0001c0001t0006g0020a0001c0001t0006g0047others(16): Show | 24 | HG01069.hp2 HG01071.hp1 HG01175.hp1 others(21): Show |
intron_variant | MODIFIER | c.1663-364G>A | MFN1 | ENSG00000171109.19 | transcript | ENST00000471841.6 | protein_coding | 14/17 | chr3 | 179385205 | ||||||
chr3:179385210
|
G | C | 2 | a0001c0001t0003g0271a0001c0001t0003g0272 | 2 | NA19240.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.1663-359G>C | MFN1 | ENSG00000171109.19 | transcript | ENST00000471841.6 | protein_coding | 14/17 | chr3 | 179385210 | ||||||
chr3:179385219
|
CT | C | 247 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0018others(244): Show | 296 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(293): Show |
intron_variant | MODIFIER | c.1663-336delT | MFN1 | ENSG00000171109.19 | transcript | ENST00000471841.6 | protein_coding | 14/17 | INFO_REALIGN_3_PRIME | chr3 | 179385219 | |||||
chr3:179385304
|
T | A | 1 | a0001c0001t0002g0177 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.1663-265T>A | MFN1 | ENSG00000171109.19 | transcript | ENST00000471841.6 | protein_coding | 14/17 | chr3 | 179385304 | ||||||
chr3:179385331
|
A | G | 1 | a0001c0001t0001g0130 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.1663-238A>G | MFN1 | ENSG00000171109.19 | transcript | ENST00000471841.6 | protein_coding | 14/17 | chr3 | 179385331 | ||||||
chr3:179385476
|
CAT | C | 79 | a0001c0001t0002g0003a0001c0001t0002g0005a0001c0001t0002g0006others(76): Show | 92 | HG00140.hp2 HG00280.hp1 HG00408.hp2 others(89): Show |
intron_variant | MODIFIER | c.1663-91_1663-90del others(2): Show |
MFN1 | ENSG00000171109.19 | transcript | ENST00000471841.6 | protein_coding | 14/17 | INFO_REALIGN_3_PRIME | chr3 | 179385476 | |||||
chr3:179385499
|
A | G | 1 | a0001c0001t0004g0092 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.1663-70A>G | MFN1 | ENSG00000171109.19 | transcript | ENST00000471841.6 | protein_coding | 14/17 | chr3 | 179385499 | ||||||
chr3:179385554
|
C | CT | 248 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0018others(245): Show | 297 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(294): Show |
splice_region_variant&intron_variant | LOW | c.1663-6dupT | MFN1 | ENSG00000171109.19 | transcript | ENST00000471841.6 | protein_coding | 14/17 | INFO_REALIGN_3_PRIME | chr3 | 179385554 | |||||
chr3:179385554
|
C | CTT | 66 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0010others(63): Show | 82 | HG00438.hp2 HG00544.hp2 HG00597.hp2 others(79): Show |
splice_region_variant&intron_variant | LOW | c.1663-7_1663-6dupTT | MFN1 | ENSG00000171109.19 | transcript | ENST00000471841.6 | protein_coding | 14/17 | INFO_REALIGN_3_PRIME | chr3 | 179385554 | |||||
chr3:179385847
|
T | A | 6 | a0001c0002t0004g0282a0001c0002t0004g0285a0001c0002t0016g0281others(3): Show | 6 | HG03669.hp1 HG03688.hp2 HG03704.hp1 others(3): Show |
intron_variant | MODIFIER | c.1815+126T>A | MFN1 | ENSG00000171109.19 | transcript | ENST00000471841.6 | protein_coding | 15/17 | chr3 | 179385847 | ||||||
chr3:179385870
|
A | C | 2 | a0001c0005t0027g0287a0001c0005t0027g0288 | 2 | HG02559.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.1815+149A>C | MFN1 | ENSG00000171109.19 | transcript | ENST00000471841.6 | protein_coding | 15/17 | chr3 | 179385870 | ||||||
chr3:179385898
|
A | T | 1 | a0001c0001t0001g0034 | 2 | NA18960.hp2 NA19056.hp2 |
intron_variant | MODIFIER | c.1815+177A>T | MFN1 | ENSG00000171109.19 | transcript | ENST00000471841.6 | protein_coding | 15/17 | chr3 | 179385898 | ||||||
chr3:179385997
|
G | A | 53 | a0001c0001t0006g0009a0001c0001t0006g0020a0001c0001t0006g0047others(50): Show | 61 | HG00735.hp2 HG01069.hp1 HG01069.hp2 others(58): Show |
intron_variant | MODIFIER | c.1815+276G>A | MFN1 | ENSG00000171109.19 | transcript | ENST00000471841.6 | protein_coding | 15/17 | chr3 | 179385997 | ||||||
chr3:179386723
|
A | T | 1 | a0001c0009t0039g0225 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.2012+94A>T | MFN1 | ENSG00000171109.19 | transcript | ENST00000471841.6 | protein_coding | 16/17 | chr3 | 179386723 | ||||||
chr3:179386828
|
T | C | 5 | a0001c0001t0019g0054a0001c0001t0019g0105a0001c0001t0019g0106others(2): Show | 5 | HG02647.hp1 HG02896.hp1 HG02965.hp1 others(2): Show |
intron_variant | MODIFIER | c.2012+199T>C | MFN1 | ENSG00000171109.19 | transcript | ENST00000471841.6 | protein_coding | 16/17 | chr3 | 179386828 | ||||||
chr3:179386857
|
A | G | 1 | a0001c0001t0007g0156 | 1 | NA19078.hp1 | intron_variant | MODIFIER | c.2012+228A>G | MFN1 | ENSG00000171109.19 | transcript | ENST00000471841.6 | protein_coding | 16/17 | chr3 | 179386857 | ||||||
chr3:179386916
|
C | A | 53 | a0001c0001t0006g0009a0001c0001t0006g0020a0001c0001t0006g0047others(50): Show | 61 | HG00735.hp2 HG01069.hp1 HG01069.hp2 others(58): Show |
intron_variant | MODIFIER | c.2012+287C>A | MFN1 | ENSG00000171109.19 | transcript | ENST00000471841.6 | protein_coding | 16/17 | chr3 | 179386916 | ||||||
chr3:179386966
|
G | A | 5 | a0001c0001t0019g0054a0001c0001t0019g0105a0001c0001t0019g0106others(2): Show | 5 | HG02647.hp1 HG02896.hp1 HG02965.hp1 others(2): Show |
intron_variant | MODIFIER | c.2012+337G>A | MFN1 | ENSG00000171109.19 | transcript | ENST00000471841.6 | protein_coding | 16/17 | chr3 | 179386966 | ||||||
chr3:179387001
|
C | T | 1 | a0001c0001t0020g0102 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.2012+372C>T | MFN1 | ENSG00000171109.19 | transcript | ENST00000471841.6 | protein_coding | 16/17 | chr3 | 179387001 | ||||||
chr3:179387046
|
G | T | 2 | a0001c0005t0027g0287a0001c0005t0027g0288 | 2 | HG02559.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.2012+417G>T | MFN1 | ENSG00000171109.19 | transcript | ENST00000471841.6 | protein_coding | 16/17 | chr3 | 179387046 | ||||||
chr3:179387193
|
A | G | 55 | a0001c0001t0006g0009a0001c0001t0006g0020a0001c0001t0006g0047others(52): Show | 63 | HG00735.hp2 HG01069.hp1 HG01069.hp2 others(60): Show |
intron_variant | MODIFIER | c.2012+564A>G | MFN1 | ENSG00000171109.19 | transcript | ENST00000471841.6 | protein_coding | 16/17 | chr3 | 179387193 | ||||||
chr3:179387301
|
A | C | 1 | a0001c0001t0007g0265 | 1 | HG01517.hp2 | intron_variant | MODIFIER | c.2012+672A>C | MFN1 | ENSG00000171109.19 | transcript | ENST00000471841.6 | protein_coding | 16/17 | chr3 | 179387301 | ||||||
chr3:179387362
|
A | G | 17 | a0001c0001t0006g0009a0001c0001t0006g0020a0001c0001t0006g0047others(14): Show | 22 | HG01069.hp2 HG01071.hp1 HG01175.hp1 others(19): Show |
intron_variant | MODIFIER | c.2012+733A>G | MFN1 | ENSG00000171109.19 | transcript | ENST00000471841.6 | protein_coding | 16/17 | chr3 | 179387362 | ||||||
chr3:179387584
|
CT | C | 117 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0007others(114): Show | 152 | HG00099.hp1 HG00099.hp2 HG00423.hp2 others(149): Show |
intron_variant | MODIFIER | c.2012+984delT | MFN1 | ENSG00000171109.19 | transcript | ENST00000471841.6 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr3 | 179387584 | |||||
chr3:179387584
|
CTT | C | 88 | a0001c0001t0001g0028a0001c0001t0001g0040a0001c0001t0001g0041others(85): Show | 104 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(101): Show |
intron_variant | MODIFIER | c.2012+983_2012+984d others(4): Show |
MFN1 | ENSG00000171109.19 | transcript | ENST00000471841.6 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr3 | 179387584 | |||||
chr3:179387584
|
CTTT | C | 13 | a0001c0001t0002g0164a0001c0001t0002g0178a0001c0001t0002g0202others(10): Show | 15 | HG00741.hp1 HG01069.hp2 HG01071.hp1 others(12): Show |
intron_variant | MODIFIER | c.2012+982_2012+984d others(5): Show |
MFN1 | ENSG00000171109.19 | transcript | ENST00000471841.6 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr3 | 179387584 | |||||
chr3:179387584
|
CTTTT | C | 30 | a0001c0001t0006g0009a0001c0001t0006g0047a0001c0001t0006g0048others(27): Show | 35 | HG00735.hp2 HG01433.hp2 HG02055.hp2 others(32): Show |
intron_variant | MODIFIER | c.2012+981_2012+984d others(6): Show |
MFN1 | ENSG00000171109.19 | transcript | ENST00000471841.6 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr3 | 179387584 | |||||
chr3:179387584
|
CTTTTTTT others(3): Show |
C | 1 | a0001c0001t0015g0300 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.2012+975_2012+984d others(12): Show |
MFN1 | ENSG00000171109.19 | transcript | ENST00000471841.6 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr3 | 179387584 | |||||
chr3:179387584
|
CTTTTTTT others(4): Show |
C | 1 | a0001c0001t0015g0299 | 1 | HG01169.hp1 | intron_variant | MODIFIER | c.2012+974_2012+984d others(13): Show |
MFN1 | ENSG00000171109.19 | transcript | ENST00000471841.6 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr3 | 179387584 | |||||
chr3:179387584
|
CTTTTTTT others(5): Show |
C | 1 | a0005c0010t0032g0208 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.2012+973_2012+984d others(14): Show |
MFN1 | ENSG00000171109.19 | transcript | ENST00000471841.6 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr3 | 179387584 | |||||
chr3:179387584
|
CTTTTTTT others(6): Show |
C | 1 | a0001c0001t0004g0083 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.2012+972_2012+984d others(15): Show |
MFN1 | ENSG00000171109.19 | transcript | ENST00000471841.6 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr3 | 179387584 | |||||
chr3:179387584
|
CTTTTTTT others(7): Show |
C | 33 | a0001c0001t0004g0001a0001c0001t0004g0026a0001c0001t0004g0069others(30): Show | 45 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(42): Show |
intron_variant | MODIFIER | c.2012+971_2012+984d others(16): Show |
MFN1 | ENSG00000171109.19 | transcript | ENST00000471841.6 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr3 | 179387584 | |||||
chr3:179387584
|
CTTTTTTT others(9): Show |
C | 8 | a0001c0002t0004g0282a0001c0002t0004g0285a0001c0002t0016g0281others(5): Show | 8 | HG02559.hp2 HG03669.hp1 HG03688.hp2 others(5): Show |
intron_variant | MODIFIER | c.2012+969_2012+984d others(18): Show |
MFN1 | ENSG00000171109.19 | transcript | ENST00000471841.6 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr3 | 179387584 | |||||
chr3:179387650
|
A | G | 1 | a0001c0001t0001g0043 | 2 | HG00099.hp1 HG00733.hp1 |
intron_variant | MODIFIER | c.2012+1021A>G | MFN1 | ENSG00000171109.19 | transcript | ENST00000471841.6 | protein_coding | 16/17 | chr3 | 179387650 | ||||||
chr3:179387729
|
A | AT | 82 | a0001c0001t0002g0003a0001c0001t0002g0005a0001c0001t0002g0006others(79): Show | 95 | HG00140.hp2 HG00280.hp1 HG00408.hp2 others(92): Show |
intron_variant | MODIFIER | c.2012+1117dupT | MFN1 | ENSG00000171109.19 | transcript | ENST00000471841.6 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr3 | 179387729 | |||||
chr3:179387729
|
AT | A | 25 | a0001c0001t0001g0231a0001c0001t0009g0024a0001c0001t0009g0025others(22): Show | 27 | HG00735.hp2 HG01069.hp1 HG01167.hp1 others(24): Show |
intron_variant | MODIFIER | c.2012+1117delT | MFN1 | ENSG00000171109.19 | transcript | ENST00000471841.6 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr3 | 179387729 | |||||
chr3:179387857
|
T | G | 1 | a0005c0010t0032g0208 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.2012+1228T>G | MFN1 | ENSG00000171109.19 | transcript | ENST00000471841.6 | protein_coding | 16/17 | chr3 | 179387857 | ||||||
chr3:179387900
|
G | T | 53 | a0001c0001t0006g0009a0001c0001t0006g0020a0001c0001t0006g0047others(50): Show | 61 | HG00735.hp2 HG01069.hp1 HG01069.hp2 others(58): Show |
intron_variant | MODIFIER | c.2012+1271G>T | MFN1 | ENSG00000171109.19 | transcript | ENST00000471841.6 | protein_coding | 16/17 | chr3 | 179387900 | ||||||
chr3:179388007
|
C | T | 1 | a0001c0009t0039g0225 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.2012+1378C>T | MFN1 | ENSG00000171109.19 | transcript | ENST00000471841.6 | protein_coding | 16/17 | chr3 | 179388007 | ||||||
chr3:179388146
|
C | T | 5 | a0001c0001t0020g0101a0001c0001t0020g0102a0001c0001t0020g0216others(2): Show | 5 | HG01433.hp1 HG02257.hp1 HG02280.hp1 others(2): Show |
intron_variant | MODIFIER | c.2012+1517C>T | MFN1 | ENSG00000171109.19 | transcript | ENST00000471841.6 | protein_coding | 16/17 | chr3 | 179388146 | ||||||
chr3:179388291
|
T | C | 6 | a0001c0001t0018g0022a0001c0001t0018g0050a0001c0001t0018g0052others(3): Show | 7 | HG01069.hp1 HG01167.hp1 HG01884.hp1 others(4): Show |
intron_variant | MODIFIER | c.2012+1662T>C | MFN1 | ENSG00000171109.19 | transcript | ENST00000471841.6 | protein_coding | 16/17 | chr3 | 179388291 | ||||||
chr3:179388390
|
A | C | 1 | a0001c0001t0001g0108 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.2013-1614A>C | MFN1 | ENSG00000171109.19 | transcript | ENST00000471841.6 | protein_coding | 16/17 | chr3 | 179388390 | ||||||
chr3:179388468
|
G | A | 3 | a0001c0001t0018g0052a0001c0001t0018g0053a0001c0001t0034g0051 | 3 | HG01167.hp1 HG02717.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.2013-1536G>A | MFN1 | ENSG00000171109.19 | transcript | ENST00000471841.6 | protein_coding | 16/17 | chr3 | 179388468 | ||||||
chr3:179388568
|
C | T | 3 | a0001c0001t0020g0101a0001c0001t0020g0102a0001c0001t0020g0216 | 3 | HG01433.hp1 HG02280.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.2013-1436C>T | MFN1 | ENSG00000171109.19 | transcript | ENST00000471841.6 | protein_coding | 16/17 | chr3 | 179388568 | ||||||
chr3:179388634
|
T | G | 1 | a0001c0001t0017g0090 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.2013-1370T>G | MFN1 | ENSG00000171109.19 | transcript | ENST00000471841.6 | protein_coding | 16/17 | chr3 | 179388634 | ||||||
chr3:179388930
|
G | T | 67 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0018others(64): Show | 83 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(80): Show |
intron_variant | MODIFIER | c.2013-1074G>T | MFN1 | ENSG00000171109.19 | transcript | ENST00000471841.6 | protein_coding | 16/17 | chr3 | 179388930 | ||||||
chr3:179388943
|
A | T | 1 | a0001c0001t0005g0148 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.2013-1061A>T | MFN1 | ENSG00000171109.19 | transcript | ENST00000471841.6 | protein_coding | 16/17 | chr3 | 179388943 | ||||||
chr3:179389059
|
G | T | 128 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0018others(125): Show | 152 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(149): Show |
intron_variant | MODIFIER | c.2013-945G>T | MFN1 | ENSG00000171109.19 | transcript | ENST00000471841.6 | protein_coding | 16/17 | chr3 | 179389059 | ||||||
chr3:179389147
|
TATTC | T | 6 | a0001c0002t0004g0282a0001c0002t0004g0285a0001c0002t0016g0281others(3): Show | 6 | HG03669.hp1 HG03688.hp2 HG03704.hp1 others(3): Show |
intron_variant | MODIFIER | c.2013-845_2013-842d others(6): Show |
MFN1 | ENSG00000171109.19 | transcript | ENST00000471841.6 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr3 | 179389147 | |||||
chr3:179389231
|
G | A | 247 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0018others(244): Show | 296 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(293): Show |
intron_variant | MODIFIER | c.2013-773G>A | MFN1 | ENSG00000171109.19 | transcript | ENST00000471841.6 | protein_coding | 16/17 | chr3 | 179389231 | ||||||
chr3:179389270
|
A | G | 2 | a0001c0001t0023g0303a0001c0001t0023g0304 | 2 | HG02257.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.2013-734A>G | MFN1 | ENSG00000171109.19 | transcript | ENST00000471841.6 | protein_coding | 16/17 | chr3 | 179389270 | ||||||
chr3:179389544
|
C | G | 2 | a0001c0001t0023g0303a0001c0001t0023g0304 | 2 | HG02257.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.2013-460C>G | MFN1 | ENSG00000171109.19 | transcript | ENST00000471841.6 | protein_coding | 16/17 | chr3 | 179389544 | ||||||
chr3:179389551
|
A | T | 1 | a0001c0001t0003g0240 | 1 | NA19089.hp1 | intron_variant | MODIFIER | c.2013-453A>T | MFN1 | ENSG00000171109.19 | transcript | ENST00000471841.6 | protein_coding | 16/17 | chr3 | 179389551 | ||||||
chr3:179389653
|
A | T | 1 | a0001c0001t0009g0289 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.2013-351A>T | MFN1 | ENSG00000171109.19 | transcript | ENST00000471841.6 | protein_coding | 16/17 | chr3 | 179389653 | ||||||
chr3:179389756
|
A | G | 53 | a0001c0001t0006g0009a0001c0001t0006g0020a0001c0001t0006g0047others(50): Show | 61 | HG00735.hp2 HG01069.hp1 HG01069.hp2 others(58): Show |
intron_variant | MODIFIER | c.2013-248A>G | MFN1 | ENSG00000171109.19 | transcript | ENST00000471841.6 | protein_coding | 16/17 | chr3 | 179389756 | ||||||
chr3:179389928
|
T | C | 1 | a0001c0001t0003g0136 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.2013-76T>C | MFN1 | ENSG00000171109.19 | transcript | ENST00000471841.6 | protein_coding | 16/17 | chr3 | 179389928 | ||||||
chr3:179389988
|
A | G | 1 | a0001c0001t0001g0277 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.2013-16A>G | MFN1 | ENSG00000171109.19 | transcript | ENST00000471841.6 | protein_coding | 16/17 | chr3 | 179389988 | ||||||
chr3:179390322
|
T | C | 1 | a0001c0001t0001g0239 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.2147+184T>C | MFN1 | ENSG00000171109.19 | transcript | ENST00000471841.6 | protein_coding | 17/17 | chr3 | 179390322 | ||||||
chr3:179390334
|
T | C | 6 | a0001c0002t0004g0282a0001c0002t0004g0285a0001c0002t0016g0281others(3): Show | 6 | HG03669.hp1 HG03688.hp2 HG03704.hp1 others(3): Show |
intron_variant | MODIFIER | c.2147+196T>C | MFN1 | ENSG00000171109.19 | transcript | ENST00000471841.6 | protein_coding | 17/17 | chr3 | 179390334 | ||||||
chr3:179390435
|
C | T | 1 | a0001c0001t0001g0277 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.2147+297C>T | MFN1 | ENSG00000171109.19 | transcript | ENST00000471841.6 | protein_coding | 17/17 | chr3 | 179390435 | ||||||
chr3:179390675
|
A | G | 7 | a0001c0001t0015g0021a0001c0001t0015g0299a0001c0001t0015g0300others(4): Show | 8 | HG01167.hp2 HG01169.hp1 HG02109.hp1 others(5): Show |
intron_variant | MODIFIER | c.2147+537A>G | MFN1 | ENSG00000171109.19 | transcript | ENST00000471841.6 | protein_coding | 17/17 | chr3 | 179390675 | ||||||
chr3:179390944
|
C | T | 1 | a0001c0001t0012g0060 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.2147+806C>T | MFN1 | ENSG00000171109.19 | transcript | ENST00000471841.6 | protein_coding | 17/17 | chr3 | 179390944 | ||||||
chr3:179391005
|
T | C | 1 | a0001c0001t0036g0210 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.2147+867T>C | MFN1 | ENSG00000171109.19 | transcript | ENST00000471841.6 | protein_coding | 17/17 | chr3 | 179391005 | ||||||
chr3:179391103
|
G | A | 1 | a0001c0001t0005g0179 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.2148-878G>A | MFN1 | ENSG00000171109.19 | transcript | ENST00000471841.6 | protein_coding | 17/17 | chr3 | 179391103 | ||||||
chr3:179391111
|
A | ACACATTT | 11 | a0001c0001t0009g0024a0001c0001t0009g0025a0001c0001t0009g0057others(8): Show | 12 | HG02257.hp2 HG02572.hp2 HG02630.hp2 others(9): Show |
intron_variant | MODIFIER | c.2148-869_2148-868i others(9): Show |
MFN1 | ENSG00000171109.19 | transcript | ENST00000471841.6 | protein_coding | 17/17 | INFO_REALIGN_3_PRIME | chr3 | 179391111 | |||||
chr3:179391113
|
T | A | 11 | a0001c0001t0009g0024a0001c0001t0009g0025a0001c0001t0009g0057others(8): Show | 12 | HG02257.hp2 HG02572.hp2 HG02630.hp2 others(9): Show |
intron_variant | MODIFIER | c.2148-868T>A | MFN1 | ENSG00000171109.19 | transcript | ENST00000471841.6 | protein_coding | 17/17 | chr3 | 179391113 | ||||||
chr3:179391114
|
G | A | 11 | a0001c0001t0009g0024a0001c0001t0009g0025a0001c0001t0009g0057others(8): Show | 12 | HG02257.hp2 HG02572.hp2 HG02630.hp2 others(9): Show |
intron_variant | MODIFIER | c.2148-867G>A | MFN1 | ENSG00000171109.19 | transcript | ENST00000471841.6 | protein_coding | 17/17 | chr3 | 179391114 | ||||||
chr3:179391129
|
G | T | 40 | a0001c0001t0004g0001a0001c0001t0004g0026a0001c0001t0004g0069others(37): Show | 52 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(49): Show |
intron_variant | MODIFIER | c.2148-852G>T | MFN1 | ENSG00000171109.19 | transcript | ENST00000471841.6 | protein_coding | 17/17 | chr3 | 179391129 | ||||||
chr3:179391391
|
A | G | 1 | a0001c0009t0039g0225 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.2148-590A>G | MFN1 | ENSG00000171109.19 | transcript | ENST00000471841.6 | protein_coding | 17/17 | chr3 | 179391391 | ||||||
chr3:179391441
|
C | T | 1 | a0001c0001t0036g0210 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.2148-540C>T | MFN1 | ENSG00000171109.19 | transcript | ENST00000471841.6 | protein_coding | 17/17 | chr3 | 179391441 | ||||||
chr3:179391808
|
A | G | 1 | a0001c0001t0014g0071 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.2148-173A>G | MFN1 | ENSG00000171109.19 | transcript | ENST00000471841.6 | protein_coding | 17/17 | chr3 | 179391808 | ||||||
chr3:179391947
|
A | G | 247 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0018others(244): Show | 296 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(293): Show |
intron_variant | MODIFIER | c.2148-34A>G | MFN1 | ENSG00000171109.19 | transcript | ENST00000471841.6 | protein_coding | 17/17 | chr3 | 179391947 |