geneid | 9927 |
---|---|
ensemblid | ENSG00000116688.18 |
hgncid | 16877 |
symbol | MFN2 |
name | mitofusin 2 |
refseq_nuc | NM_014874.4 |
refseq_prot | NP_055689.1 |
ensembl_nuc | ENST00000235329.10 |
ensembl_prot | ENSP00000235329.5 |
mane_status | MANE Select |
chr | chr1 |
start | 11980444 |
end | 12013508 |
strand | + |
ver | v1.2 |
region | chr1:11980444-12013508 |
region5000 | chr1:11975444-12018508 |
regionname0 | MFN2_chr1_11980444_12013508 |
regionname5000 | MFN2_chr1_11975444_12018508 |
ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 1/1 | 757 | 389 | 91 | 64 | 172 | 14 | 46 | 134 | MFN2_chr1_11975444_12018508 | MFN2 | copy fasta | chr1 | 11975444 | 12018508 |
a0002 | 0/0 | 757 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | MFN2_chr1_11975444_12018508 | MFN2 | copy fasta | chr1 | 11975444 | 12018508 |
a0003 | 0/0 | 757 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | MFN2_chr1_11975444_12018508 | MFN2 | copy fasta | chr1 | 11975444 | 12018508 |
a0004 | 0/0 | 757 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | MFN2_chr1_11975444_12018508 | MFN2 | copy fasta | chr1 | 11975444 | 12018508 |
a0005 | 0/0 | 757 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | MFN2_chr1_11975444_12018508 | MFN2 | copy fasta | chr1 | 11975444 | 12018508 |
chapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
c0001 | 1/0 | 2274 | 340 | 78 | 58 | 150 | 14 | 39 | MFN2_chr1_11975444_12018508 | MFN2 | copy fasta | chr1 | 11975444 | 12018508 |
c0002 | 0/0 | 2274 | 21 | 1 | 3 | 12 | 0 | 5 | MFN2_chr1_11975444_12018508 | MFN2 | copy fasta | chr1 | 11975444 | 12018508 |
c0003 | 0/0 | 2274 | 8 | 6 | 2 | 0 | 0 | 0 | MFN2_chr1_11975444_12018508 | MFN2 | copy fasta | chr1 | 11975444 | 12018508 |
c0004 | 0/0 | 2274 | 6 | 0 | 0 | 6 | 0 | 0 | MFN2_chr1_11975444_12018508 | MFN2 | copy fasta | chr1 | 11975444 | 12018508 |
c0005 | 0/0 | 2274 | 3 | 3 | 0 | 0 | 0 | 0 | MFN2_chr1_11975444_12018508 | MFN2 | copy fasta | chr1 | 11975444 | 12018508 |
c0006 | 0/1 | 2274 | 3 | 1 | 0 | 0 | 0 | 1 | MFN2_chr1_11975444_12018508 | MFN2 | copy fasta | chr1 | 11975444 | 12018508 |
c0007 | 0/0 | 2274 | 2 | 2 | 0 | 0 | 0 | 0 | MFN2_chr1_11975444_12018508 | MFN2 | copy fasta | chr1 | 11975444 | 12018508 |
c0008 | 0/0 | 2274 | 2 | 0 | 0 | 1 | 0 | 1 | MFN2_chr1_11975444_12018508 | MFN2 | copy fasta | chr1 | 11975444 | 12018508 |
c0009 | 0/0 | 2274 | 1 | 0 | 0 | 1 | 0 | 0 | MFN2_chr1_11975444_12018508 | MFN2 | copy fasta | chr1 | 11975444 | 12018508 |
c0010 | 0/0 | 2274 | 1 | 1 | 0 | 0 | 0 | 0 | MFN2_chr1_11975444_12018508 | MFN2 | copy fasta | chr1 | 11975444 | 12018508 |
c0011 | 0/0 | 2274 | 1 | 0 | 0 | 1 | 0 | 0 | MFN2_chr1_11975444_12018508 | MFN2 | copy fasta | chr1 | 11975444 | 12018508 |
c0012 | 0/0 | 2274 | 1 | 0 | 1 | 0 | 0 | 0 | MFN2_chr1_11975444_12018508 | MFN2 | copy fasta | chr1 | 11975444 | 12018508 |
c0013 | 0/0 | 2274 | 1 | 0 | 0 | 1 | 0 | 0 | MFN2_chr1_11975444_12018508 | MFN2 | copy fasta | chr1 | 11975444 | 12018508 |
c0014 | 0/0 | 2274 | 1 | 1 | 0 | 0 | 0 | 0 | MFN2_chr1_11975444_12018508 | MFN2 | copy fasta | chr1 | 11975444 | 12018508 |
c0015 | 0/0 | 2274 | 1 | 0 | 0 | 1 | 0 | 0 | MFN2_chr1_11975444_12018508 | MFN2 | copy fasta | chr1 | 11975444 | 12018508 |
c0016 | 0/0 | 2274 | 1 | 1 | 0 | 0 | 0 | 0 | MFN2_chr1_11975444_12018508 | MFN2 | copy fasta | chr1 | 11975444 | 12018508 |
c0017 | 0/0 | 2274 | 1 | 0 | 0 | 1 | 0 | 0 | MFN2_chr1_11975444_12018508 | MFN2 | copy fasta | chr1 | 11975444 | 12018508 |
thapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
t0001 | 0/1 | 2134 | 129 | 27 | 28 | 50 | 6 | 17 | MFN2_chr1_11975444_12018508 | MFN2 | copy fasta | chr1 | 11975444 | 12018508 |
t0002 | 1/0 | 2134 | 96 | 7 | 24 | 51 | 5 | 8 | MFN2_chr1_11975444_12018508 | MFN2 | copy fasta | chr1 | 11975444 | 12018508 |
t0003 | 0/0 | 2134 | 59 | 0 | 5 | 41 | 2 | 11 | MFN2_chr1_11975444_12018508 | MFN2 | copy fasta | chr1 | 11975444 | 12018508 |
t0004 | 0/0 | 2134 | 39 | 28 | 1 | 9 | 0 | 1 | MFN2_chr1_11975444_12018508 | MFN2 | copy fasta | chr1 | 11975444 | 12018508 |
t0005 | 0/0 | 2134 | 16 | 1 | 3 | 7 | 0 | 5 | MFN2_chr1_11975444_12018508 | MFN2 | copy fasta | chr1 | 11975444 | 12018508 |
t0006 | 0/0 | 2134 | 7 | 6 | 1 | 0 | 0 | 0 | MFN2_chr1_11975444_12018508 | MFN2 | copy fasta | chr1 | 11975444 | 12018508 |
t0007 | 0/0 | 2135 | 6 | 5 | 1 | 0 | 0 | 0 | MFN2_chr1_11975444_12018508 | MFN2 | copy fasta | chr1 | 11975444 | 12018508 |
t0008 | 0/0 | 2134 | 6 | 0 | 0 | 6 | 0 | 0 | MFN2_chr1_11975444_12018508 | MFN2 | copy fasta | chr1 | 11975444 | 12018508 |
t0009 | 0/0 | 2134 | 4 | 0 | 0 | 4 | 0 | 0 | MFN2_chr1_11975444_12018508 | MFN2 | copy fasta | chr1 | 11975444 | 12018508 |
t0010 | 0/0 | 2134 | 3 | 3 | 0 | 0 | 0 | 0 | MFN2_chr1_11975444_12018508 | MFN2 | copy fasta | chr1 | 11975444 | 12018508 |
t0011 | 0/0 | 2133 | 3 | 0 | 0 | 3 | 0 | 0 | MFN2_chr1_11975444_12018508 | MFN2 | copy fasta | chr1 | 11975444 | 12018508 |
t0012 | 0/0 | 2134 | 3 | 3 | 0 | 0 | 0 | 0 | MFN2_chr1_11975444_12018508 | MFN2 | copy fasta | chr1 | 11975444 | 12018508 |
t0013 | 0/0 | 2134 | 3 | 3 | 0 | 0 | 0 | 0 | MFN2_chr1_11975444_12018508 | MFN2 | copy fasta | chr1 | 11975444 | 12018508 |
t0014 | 0/0 | 2134 | 3 | 3 | 0 | 0 | 0 | 0 | MFN2_chr1_11975444_12018508 | MFN2 | copy fasta | chr1 | 11975444 | 12018508 |
t0015 | 0/0 | 2134 | 3 | 3 | 0 | 0 | 0 | 0 | MFN2_chr1_11975444_12018508 | MFN2 | copy fasta | chr1 | 11975444 | 12018508 |
t0016 | 0/0 | 2134 | 2 | 0 | 0 | 0 | 0 | 2 | MFN2_chr1_11975444_12018508 | MFN2 | copy fasta | chr1 | 11975444 | 12018508 |
t0017 | 0/0 | 2135 | 2 | 1 | 1 | 0 | 0 | 0 | MFN2_chr1_11975444_12018508 | MFN2 | copy fasta | chr1 | 11975444 | 12018508 |
t0018 | 0/0 | 2134 | 1 | 0 | 0 | 0 | 0 | 1 | MFN2_chr1_11975444_12018508 | MFN2 | copy fasta | chr1 | 11975444 | 12018508 |
t0019 | 0/0 | 2134 | 1 | 0 | 0 | 0 | 0 | 1 | MFN2_chr1_11975444_12018508 | MFN2 | copy fasta | chr1 | 11975444 | 12018508 |
t0020 | 0/0 | 2133 | 1 | 0 | 0 | 1 | 0 | 0 | MFN2_chr1_11975444_12018508 | MFN2 | copy fasta | chr1 | 11975444 | 12018508 |
t0021 | 0/0 | 2134 | 1 | 0 | 0 | 1 | 0 | 0 | MFN2_chr1_11975444_12018508 | MFN2 | copy fasta | chr1 | 11975444 | 12018508 |
t0022 | 0/0 | 2134 | 1 | 1 | 0 | 0 | 0 | 0 | MFN2_chr1_11975444_12018508 | MFN2 | copy fasta | chr1 | 11975444 | 12018508 |
t0023 | 0/0 | 2135 | 1 | 0 | 0 | 1 | 0 | 0 | MFN2_chr1_11975444_12018508 | MFN2 | copy fasta | chr1 | 11975444 | 12018508 |
t0024 | 0/0 | 2134 | 1 | 0 | 0 | 0 | 1 | 0 | MFN2_chr1_11975444_12018508 | MFN2 | copy fasta | chr1 | 11975444 | 12018508 |
t0025 | 0/0 | 2134 | 1 | 1 | 0 | 0 | 0 | 0 | MFN2_chr1_11975444_12018508 | MFN2 | copy fasta | chr1 | 11975444 | 12018508 |
t0026 | 0/0 | 2134 | 1 | 1 | 0 | 0 | 0 | 0 | MFN2_chr1_11975444_12018508 | MFN2 | copy fasta | chr1 | 11975444 | 12018508 |
t0027 | 0/0 | 2134 | 1 | 1 | 0 | 0 | 0 | 0 | MFN2_chr1_11975444_12018508 | MFN2 | copy fasta | chr1 | 11975444 | 12018508 |
ghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
g0001 | 0/0 | 21 | 2 | 1 | 17 | 1 | 0 | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
g0002 | 0/0 | 8 | 1 | 7 | 0 | 0 | 0 | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
g0003 | 0/0 | 8 | 0 | 0 | 7 | 1 | 0 | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
g0004 | 0/0 | 7 | 0 | 0 | 5 | 0 | 2 | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
g0005 | 0/0 | 5 | 1 | 3 | 0 | 0 | 1 | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
g0006 | 0/0 | 4 | 0 | 4 | 0 | 0 | 0 | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
g0007 | 0/0 | 4 | 1 | 0 | 3 | 0 | 0 | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
g0008 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
g0009 | 0/0 | 4 | 0 | 0 | 3 | 0 | 1 | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
g0010 | 0/0 | 4 | 0 | 4 | 0 | 0 | 0 | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
g0011 | 0/0 | 3 | 1 | 2 | 0 | 0 | 0 | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
g0012 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
g0013 | 0/0 | 3 | 0 | 1 | 1 | 1 | 0 | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
g0014 | 0/0 | 3 | 1 | 1 | 1 | 0 | 0 | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
g0015 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
g0016 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
g0017 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
g0018 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
g0019 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
g0020 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
g0021 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
g0022 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
g0023 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
g0024 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
g0025 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
g0026 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
g0027 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
g0028 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
g0029 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
g0030 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
g0031 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
g0032 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
g0033 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
g0034 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
g0035 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
g0036 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
g0046 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
g0056 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
g0061 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
g0063 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
g0064 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
g0066 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
g0067 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
g0068 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
g0070 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
g0071 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
g0072 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
g0074 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
g0077 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
g0081 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
g0084 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
g0086 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
g0088 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
g0089 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
g0092 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
g0093 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
g0094 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
g0095 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
g0098 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
g0101 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
g0103 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
g0104 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
g0106 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
g0107 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
g0109 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
g0110 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
g0123 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
g0124 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
g0125 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
g0126 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
g0127 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
g0128 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
g0131 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
g0138 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
g0141 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
g0143 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
g0145 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
g0149 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
g0151 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
g0155 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
g0157 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
g0161 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
g0162 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
g0183 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
g0189 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
g0199 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
g0202 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
g0203 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
g0205 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
g0209 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
g0210 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
g0212 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
g0213 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
g0221 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
g0227 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
g0230 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
g0231 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
g0233 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
g0235 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
g0240 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
g0246 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
g0251 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
g0252 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
g0254 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
g0255 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
g0257 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
g0259 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
g0263 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
g0264 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
g0270 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
g0272 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
g0273 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
g0275 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
g0280 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
g0281 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
g0282 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
g0283 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
g0284 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
g0286 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
g0287 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
g0288 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
g0290 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
g0291 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
g0292 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
g0293 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
g0294 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
g0295 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
g0296 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
g0297 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
g0298 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
g0299 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
g0300 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
g0301 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
g0302 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
achapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 1/0 | 2274 | 340 | 78 | 58 | 150 | 14 | 39 | MFN2_chr1_11975444_12018508 | MFN2 | copy fasta | chr1 | 11975444 | 12018508 |
a0001c0002 | 0/0 | 2274 | 21 | 1 | 3 | 12 | 0 | 5 | MFN2_chr1_11975444_12018508 | MFN2 | copy fasta | chr1 | 11975444 | 12018508 |
a0001c0003 | 0/0 | 2274 | 8 | 6 | 2 | 0 | 0 | 0 | MFN2_chr1_11975444_12018508 | MFN2 | copy fasta | chr1 | 11975444 | 12018508 |
a0001c0004 | 0/0 | 2274 | 6 | 0 | 0 | 6 | 0 | 0 | MFN2_chr1_11975444_12018508 | MFN2 | copy fasta | chr1 | 11975444 | 12018508 |
a0001c0005 | 0/0 | 2274 | 3 | 3 | 0 | 0 | 0 | 0 | MFN2_chr1_11975444_12018508 | MFN2 | copy fasta | chr1 | 11975444 | 12018508 |
a0001c0006 | 0/1 | 2274 | 3 | 1 | 0 | 0 | 0 | 1 | MFN2_chr1_11975444_12018508 | MFN2 | copy fasta | chr1 | 11975444 | 12018508 |
a0001c0008 | 0/0 | 2274 | 2 | 0 | 0 | 1 | 0 | 1 | MFN2_chr1_11975444_12018508 | MFN2 | copy fasta | chr1 | 11975444 | 12018508 |
a0001c0009 | 0/0 | 2274 | 1 | 0 | 0 | 1 | 0 | 0 | MFN2_chr1_11975444_12018508 | MFN2 | copy fasta | chr1 | 11975444 | 12018508 |
a0001c0012 | 0/0 | 2274 | 1 | 0 | 1 | 0 | 0 | 0 | MFN2_chr1_11975444_12018508 | MFN2 | copy fasta | chr1 | 11975444 | 12018508 |
a0001c0013 | 0/0 | 2274 | 1 | 0 | 0 | 1 | 0 | 0 | MFN2_chr1_11975444_12018508 | MFN2 | copy fasta | chr1 | 11975444 | 12018508 |
a0001c0014 | 0/0 | 2274 | 1 | 1 | 0 | 0 | 0 | 0 | MFN2_chr1_11975444_12018508 | MFN2 | copy fasta | chr1 | 11975444 | 12018508 |
a0001c0016 | 0/0 | 2274 | 1 | 1 | 0 | 0 | 0 | 0 | MFN2_chr1_11975444_12018508 | MFN2 | copy fasta | chr1 | 11975444 | 12018508 |
a0001c0017 | 0/0 | 2274 | 1 | 0 | 0 | 1 | 0 | 0 | MFN2_chr1_11975444_12018508 | MFN2 | copy fasta | chr1 | 11975444 | 12018508 |
a0002c0007 | 0/0 | 2274 | 2 | 2 | 0 | 0 | 0 | 0 | MFN2_chr1_11975444_12018508 | MFN2 | copy fasta | chr1 | 11975444 | 12018508 |
a0003c0010 | 0/0 | 2274 | 1 | 1 | 0 | 0 | 0 | 0 | MFN2_chr1_11975444_12018508 | MFN2 | copy fasta | chr1 | 11975444 | 12018508 |
a0004c0011 | 0/0 | 2274 | 1 | 0 | 0 | 1 | 0 | 0 | MFN2_chr1_11975444_12018508 | MFN2 | copy fasta | chr1 | 11975444 | 12018508 |
a0005c0015 | 0/0 | 2274 | 1 | 0 | 0 | 1 | 0 | 0 | MFN2_chr1_11975444_12018508 | MFN2 | copy fasta | chr1 | 11975444 | 12018508 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 0/0 | 4407 | 123 | 26 | 27 | 48 | 6 | 16 | MFN2_chr1_11975444_12018508 | MFN2 | copy fasta | chr1 | 11975444 | 12018508 |
a0001c0001t0002 | 1/0 | 4407 | 91 | 4 | 24 | 49 | 5 | 8 | MFN2_chr1_11975444_12018508 | MFN2 | copy fasta | chr1 | 11975444 | 12018508 |
a0001c0001t0003 | 0/0 | 4407 | 59 | 0 | 5 | 41 | 2 | 11 | MFN2_chr1_11975444_12018508 | MFN2 | copy fasta | chr1 | 11975444 | 12018508 |
a0001c0001t0004 | 0/0 | 4407 | 27 | 24 | 1 | 2 | 0 | 0 | MFN2_chr1_11975444_12018508 | MFN2 | copy fasta | chr1 | 11975444 | 12018508 |
a0001c0001t0006 | 0/0 | 4407 | 6 | 5 | 1 | 0 | 0 | 0 | MFN2_chr1_11975444_12018508 | MFN2 | copy fasta | chr1 | 11975444 | 12018508 |
a0001c0001t0009 | 0/0 | 4407 | 4 | 0 | 0 | 4 | 0 | 0 | MFN2_chr1_11975444_12018508 | MFN2 | copy fasta | chr1 | 11975444 | 12018508 |
a0001c0001t0010 | 0/0 | 4407 | 3 | 3 | 0 | 0 | 0 | 0 | MFN2_chr1_11975444_12018508 | MFN2 | copy fasta | chr1 | 11975444 | 12018508 |
a0001c0001t0011 | 0/0 | 4406 | 3 | 0 | 0 | 3 | 0 | 0 | MFN2_chr1_11975444_12018508 | MFN2 | copy fasta | chr1 | 11975444 | 12018508 |
a0001c0001t0012 | 0/0 | 4407 | 3 | 3 | 0 | 0 | 0 | 0 | MFN2_chr1_11975444_12018508 | MFN2 | copy fasta | chr1 | 11975444 | 12018508 |
a0001c0001t0013 | 0/0 | 4407 | 3 | 3 | 0 | 0 | 0 | 0 | MFN2_chr1_11975444_12018508 | MFN2 | copy fasta | chr1 | 11975444 | 12018508 |
a0001c0001t0014 | 0/0 | 4407 | 3 | 3 | 0 | 0 | 0 | 0 | MFN2_chr1_11975444_12018508 | MFN2 | copy fasta | chr1 | 11975444 | 12018508 |
a0001c0001t0015 | 0/0 | 4407 | 3 | 3 | 0 | 0 | 0 | 0 | MFN2_chr1_11975444_12018508 | MFN2 | copy fasta | chr1 | 11975444 | 12018508 |
a0001c0001t0016 | 0/0 | 4407 | 2 | 0 | 0 | 0 | 0 | 2 | MFN2_chr1_11975444_12018508 | MFN2 | copy fasta | chr1 | 11975444 | 12018508 |
a0001c0001t0018 | 0/0 | 4407 | 1 | 0 | 0 | 0 | 0 | 1 | MFN2_chr1_11975444_12018508 | MFN2 | copy fasta | chr1 | 11975444 | 12018508 |
a0001c0001t0019 | 0/0 | 4407 | 1 | 0 | 0 | 0 | 0 | 1 | MFN2_chr1_11975444_12018508 | MFN2 | copy fasta | chr1 | 11975444 | 12018508 |
a0001c0001t0020 | 0/0 | 4406 | 1 | 0 | 0 | 1 | 0 | 0 | MFN2_chr1_11975444_12018508 | MFN2 | copy fasta | chr1 | 11975444 | 12018508 |
a0001c0001t0021 | 0/0 | 4407 | 1 | 0 | 0 | 1 | 0 | 0 | MFN2_chr1_11975444_12018508 | MFN2 | copy fasta | chr1 | 11975444 | 12018508 |
a0001c0001t0022 | 0/0 | 4407 | 1 | 1 | 0 | 0 | 0 | 0 | MFN2_chr1_11975444_12018508 | MFN2 | copy fasta | chr1 | 11975444 | 12018508 |
a0001c0001t0023 | 0/0 | 4408 | 1 | 0 | 0 | 1 | 0 | 0 | MFN2_chr1_11975444_12018508 | MFN2 | copy fasta | chr1 | 11975444 | 12018508 |
a0001c0001t0024 | 0/0 | 4407 | 1 | 0 | 0 | 0 | 1 | 0 | MFN2_chr1_11975444_12018508 | MFN2 | copy fasta | chr1 | 11975444 | 12018508 |
a0001c0001t0025 | 0/0 | 4407 | 1 | 1 | 0 | 0 | 0 | 0 | MFN2_chr1_11975444_12018508 | MFN2 | copy fasta | chr1 | 11975444 | 12018508 |
a0001c0001t0026 | 0/0 | 4407 | 1 | 1 | 0 | 0 | 0 | 0 | MFN2_chr1_11975444_12018508 | MFN2 | copy fasta | chr1 | 11975444 | 12018508 |
a0001c0001t0027 | 0/0 | 4407 | 1 | 1 | 0 | 0 | 0 | 0 | MFN2_chr1_11975444_12018508 | MFN2 | copy fasta | chr1 | 11975444 | 12018508 |
a0001c0002t0005 | 0/0 | 4407 | 16 | 1 | 3 | 7 | 0 | 5 | MFN2_chr1_11975444_12018508 | MFN2 | copy fasta | chr1 | 11975444 | 12018508 |
a0001c0002t0008 | 0/0 | 4407 | 5 | 0 | 0 | 5 | 0 | 0 | MFN2_chr1_11975444_12018508 | MFN2 | copy fasta | chr1 | 11975444 | 12018508 |
a0001c0003t0007 | 0/0 | 4408 | 6 | 5 | 1 | 0 | 0 | 0 | MFN2_chr1_11975444_12018508 | MFN2 | copy fasta | chr1 | 11975444 | 12018508 |
a0001c0003t0017 | 0/0 | 4408 | 2 | 1 | 1 | 0 | 0 | 0 | MFN2_chr1_11975444_12018508 | MFN2 | copy fasta | chr1 | 11975444 | 12018508 |
a0001c0004t0004 | 0/0 | 4407 | 6 | 0 | 0 | 6 | 0 | 0 | MFN2_chr1_11975444_12018508 | MFN2 | copy fasta | chr1 | 11975444 | 12018508 |
a0001c0005t0004 | 0/0 | 4407 | 3 | 3 | 0 | 0 | 0 | 0 | MFN2_chr1_11975444_12018508 | MFN2 | copy fasta | chr1 | 11975444 | 12018508 |
a0001c0006t0001 | 0/1 | 4407 | 3 | 1 | 0 | 0 | 0 | 1 | MFN2_chr1_11975444_12018508 | MFN2 | copy fasta | chr1 | 11975444 | 12018508 |
a0001c0008t0004 | 0/0 | 4407 | 2 | 0 | 0 | 1 | 0 | 1 | MFN2_chr1_11975444_12018508 | MFN2 | copy fasta | chr1 | 11975444 | 12018508 |
a0001c0009t0002 | 0/0 | 4407 | 1 | 0 | 0 | 1 | 0 | 0 | MFN2_chr1_11975444_12018508 | MFN2 | copy fasta | chr1 | 11975444 | 12018508 |
a0001c0012t0001 | 0/0 | 4407 | 1 | 0 | 1 | 0 | 0 | 0 | MFN2_chr1_11975444_12018508 | MFN2 | copy fasta | chr1 | 11975444 | 12018508 |
a0001c0013t0002 | 0/0 | 4407 | 1 | 0 | 0 | 1 | 0 | 0 | MFN2_chr1_11975444_12018508 | MFN2 | copy fasta | chr1 | 11975444 | 12018508 |
a0001c0014t0006 | 0/0 | 4407 | 1 | 1 | 0 | 0 | 0 | 0 | MFN2_chr1_11975444_12018508 | MFN2 | copy fasta | chr1 | 11975444 | 12018508 |
a0001c0016t0004 | 0/0 | 4407 | 1 | 1 | 0 | 0 | 0 | 0 | MFN2_chr1_11975444_12018508 | MFN2 | copy fasta | chr1 | 11975444 | 12018508 |
a0001c0017t0001 | 0/0 | 4407 | 1 | 0 | 0 | 1 | 0 | 0 | MFN2_chr1_11975444_12018508 | MFN2 | copy fasta | chr1 | 11975444 | 12018508 |
a0002c0007t0002 | 0/0 | 4407 | 2 | 2 | 0 | 0 | 0 | 0 | MFN2_chr1_11975444_12018508 | MFN2 | copy fasta | chr1 | 11975444 | 12018508 |
a0003c0010t0002 | 0/0 | 4407 | 1 | 1 | 0 | 0 | 0 | 0 | MFN2_chr1_11975444_12018508 | MFN2 | copy fasta | chr1 | 11975444 | 12018508 |
a0004c0011t0001 | 0/0 | 4407 | 1 | 0 | 0 | 1 | 0 | 0 | MFN2_chr1_11975444_12018508 | MFN2 | copy fasta | chr1 | 11975444 | 12018508 |
a0005c0015t0008 | 0/0 | 4407 | 1 | 0 | 0 | 1 | 0 | 0 | MFN2_chr1_11975444_12018508 | MFN2 | copy fasta | chr1 | 11975444 | 12018508 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0001 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
a0001c0001t0001g0004 | 0/0 | 7 | 0 | 0 | 5 | 0 | 2 | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
a0001c0001t0001g0005 | 0/0 | 3 | 0 | 2 | 0 | 0 | 1 | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
a0001c0001t0001g0008 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
a0001c0001t0001g0009 | 0/0 | 4 | 0 | 0 | 3 | 0 | 1 | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
a0001c0001t0001g0010 | 0/0 | 4 | 0 | 4 | 0 | 0 | 0 | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
a0001c0001t0001g0011 | 0/0 | 3 | 1 | 2 | 0 | 0 | 0 | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
a0001c0001t0001g0013 | 0/0 | 3 | 0 | 1 | 1 | 1 | 0 | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
a0001c0001t0001g0014 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
a0001c0001t0001g0015 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
a0001c0001t0001g0018 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
a0001c0001t0001g0019 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
a0001c0001t0001g0028 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
a0001c0001t0001g0029 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
a0001c0001t0001g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
a0001c0001t0001g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
a0001c0001t0001g0071 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
a0001c0001t0001g0072 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
a0001c0001t0001g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
a0001c0001t0001g0074 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
a0001c0001t0001g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
a0001c0001t0001g0084 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
a0001c0001t0001g0093 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
a0001c0001t0001g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
a0001c0001t0001g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
a0001c0001t0001g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
a0001c0001t0001g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
a0001c0001t0001g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
a0001c0001t0001g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
a0001c0001t0001g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
a0001c0001t0001g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
a0001c0001t0001g0125 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
a0001c0001t0001g0126 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
a0001c0001t0001g0127 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
a0001c0001t0001g0128 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
a0001c0001t0001g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
a0001c0001t0001g0131 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
a0001c0001t0001g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
a0001c0001t0001g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
a0001c0001t0001g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
a0001c0001t0001g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
a0001c0001t0001g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
a0001c0001t0001g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
a0001c0001t0001g0138 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
a0001c0001t0001g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
a0001c0001t0001g0141 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
a0001c0001t0001g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
a0001c0001t0001g0143 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
a0001c0001t0001g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
a0001c0001t0001g0145 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
a0001c0001t0001g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
a0001c0001t0001g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
a0001c0001t0001g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
a0001c0001t0001g0149 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
a0001c0001t0001g0151 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
a0001c0001t0001g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
a0001c0001t0001g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
a0001c0001t0001g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
a0001c0001t0001g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
a0001c0001t0001g0157 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
a0001c0001t0001g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
a0001c0001t0001g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
a0001c0001t0001g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
a0001c0001t0001g0161 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
a0001c0001t0001g0162 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
a0001c0001t0001g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
a0001c0001t0001g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
a0001c0001t0001g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
a0001c0001t0001g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
a0001c0001t0001g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
a0001c0001t0001g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
a0001c0001t0001g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
a0001c0001t0001g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
a0001c0001t0001g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
a0001c0001t0001g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
a0001c0001t0001g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
a0001c0001t0001g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
a0001c0001t0001g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
a0001c0001t0001g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
a0001c0001t0001g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
a0001c0001t0001g0183 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
a0001c0001t0001g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
a0001c0001t0001g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
a0001c0001t0001g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
a0001c0001t0001g0203 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
a0001c0001t0001g0205 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
a0001c0001t0001g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
a0001c0001t0001g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
a0001c0001t0001g0212 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
a0001c0001t0001g0213 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
a0001c0001t0001g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
a0001c0001t0001g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
a0001c0001t0001g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
a0001c0001t0001g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
a0001c0001t0001g0286 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
a0001c0001t0001g0287 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
a0001c0001t0001g0288 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
a0001c0001t0001g0290 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
a0001c0001t0001g0299 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
a0001c0001t0002g0001 | 0/0 | 16 | 1 | 1 | 13 | 1 | 0 | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
a0001c0001t0002g0002 | 0/0 | 7 | 1 | 6 | 0 | 0 | 0 | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
a0001c0001t0002g0006 | 0/0 | 4 | 0 | 4 | 0 | 0 | 0 | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
a0001c0001t0002g0007 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
a0001c0001t0002g0008 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
a0001c0001t0002g0012 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
a0001c0001t0002g0017 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
a0001c0001t0002g0021 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
a0001c0001t0002g0022 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
a0001c0001t0002g0023 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
a0001c0001t0002g0024 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
a0001c0001t0002g0025 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
a0001c0001t0002g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
a0001c0001t0002g0027 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
a0001c0001t0002g0056 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
a0001c0001t0002g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
a0001c0001t0002g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
a0001c0001t0002g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
a0001c0001t0002g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
a0001c0001t0002g0061 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
a0001c0001t0002g0064 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
a0001c0001t0002g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
a0001c0001t0002g0066 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
a0001c0001t0002g0067 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
a0001c0001t0002g0068 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
a0001c0001t0002g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
a0001c0001t0002g0070 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
a0001c0001t0002g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
a0001c0001t0002g0077 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
a0001c0001t0002g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
a0001c0001t0002g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
a0001c0001t0002g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
a0001c0001t0002g0081 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
a0001c0001t0002g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
a0001c0001t0002g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
a0001c0001t0002g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
a0001c0001t0002g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
a0001c0001t0002g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
a0001c0001t0002g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
a0001c0001t0002g0092 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
a0001c0001t0002g0094 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
a0001c0001t0002g0095 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
a0001c0001t0002g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
a0001c0001t0002g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
a0001c0001t0002g0098 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
a0001c0001t0002g0101 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
a0001c0001t0002g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
a0001c0001t0002g0103 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
a0001c0001t0002g0104 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
a0001c0001t0002g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
a0001c0001t0002g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
a0001c0001t0002g0109 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
a0001c0001t0002g0110 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
a0001c0001t0002g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
a0001c0001t0002g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
a0001c0001t0002g0273 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
a0001c0001t0002g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
a0001c0001t0003g0003 | 0/0 | 7 | 0 | 0 | 7 | 0 | 0 | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
a0001c0001t0003g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
a0001c0001t0003g0123 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
a0001c0001t0003g0124 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
a0001c0001t0003g0155 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
a0001c0001t0003g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
a0001c0001t0003g0189 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
a0001c0001t0003g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
a0001c0001t0003g0199 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
a0001c0001t0003g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
a0001c0001t0003g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
a0001c0001t0003g0202 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
a0001c0001t0003g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
a0001c0001t0003g0209 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
a0001c0001t0003g0210 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
a0001c0001t0003g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
a0001c0001t0003g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
a0001c0001t0003g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
a0001c0001t0003g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
a0001c0001t0003g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
a0001c0001t0003g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
a0001c0001t0003g0221 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
a0001c0001t0003g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
a0001c0001t0003g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
a0001c0001t0003g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
a0001c0001t0003g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
a0001c0001t0003g0227 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
a0001c0001t0003g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
a0001c0001t0003g0230 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
a0001c0001t0003g0231 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
a0001c0001t0003g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
a0001c0001t0003g0233 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
a0001c0001t0003g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
a0001c0001t0003g0235 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
a0001c0001t0003g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
a0001c0001t0003g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
a0001c0001t0003g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
a0001c0001t0003g0240 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
a0001c0001t0003g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
a0001c0001t0003g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
a0001c0001t0003g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
a0001c0001t0003g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
a0001c0001t0003g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
a0001c0001t0003g0246 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
a0001c0001t0003g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
a0001c0001t0003g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
a0001c0001t0003g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
a0001c0001t0003g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
a0001c0001t0003g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
a0001c0001t0003g0275 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
a0001c0001t0003g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
a0001c0001t0003g0291 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
a0001c0001t0003g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
a0001c0001t0004g0002 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
a0001c0001t0004g0007 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
a0001c0001t0004g0012 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
a0001c0001t0004g0016 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
a0001c0001t0004g0030 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
a0001c0001t0004g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
a0001c0001t0004g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
a0001c0001t0004g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
a0001c0001t0004g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
a0001c0001t0004g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
a0001c0001t0004g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
a0001c0001t0004g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
a0001c0001t0004g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
a0001c0001t0004g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
a0001c0001t0004g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
a0001c0001t0004g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
a0001c0001t0004g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
a0001c0001t0004g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
a0001c0001t0004g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
a0001c0001t0004g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
a0001c0001t0004g0284 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
a0001c0001t0004g0296 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
a0001c0001t0004g0297 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
a0001c0001t0004g0298 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
a0001c0001t0006g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
a0001c0001t0006g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
a0001c0001t0006g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
a0001c0001t0006g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
a0001c0001t0006g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
a0001c0001t0006g0046 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
a0001c0001t0009g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
a0001c0001t0009g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
a0001c0001t0009g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
a0001c0001t0009g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
a0001c0001t0010g0020 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
a0001c0001t0010g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
a0001c0001t0011g0001 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
a0001c0001t0011g0008 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
a0001c0001t0012g0036 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
a0001c0001t0012g0302 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
a0001c0001t0013g0032 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
a0001c0001t0013g0251 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
a0001c0001t0014g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
a0001c0001t0014g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
a0001c0001t0014g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
a0001c0001t0015g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
a0001c0001t0015g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
a0001c0001t0015g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
a0001c0001t0016g0086 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
a0001c0001t0016g0088 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
a0001c0001t0018g0106 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
a0001c0001t0019g0107 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
a0001c0001t0020g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
a0001c0001t0021g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
a0001c0001t0022g0005 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
a0001c0001t0023g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
a0001c0001t0024g0003 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
a0001c0001t0025g0301 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
a0001c0001t0026g0272 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
a0001c0001t0027g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
a0001c0002t0005g0033 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
a0001c0002t0005g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
a0001c0002t0005g0089 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
a0001c0002t0005g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
a0001c0002t0005g0252 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
a0001c0002t0005g0254 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
a0001c0002t0005g0255 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
a0001c0002t0005g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
a0001c0002t0005g0257 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
a0001c0002t0005g0259 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
a0001c0002t0005g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
a0001c0002t0005g0263 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
a0001c0002t0005g0264 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
a0001c0002t0005g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
a0001c0002t0005g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
a0001c0002t0008g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
a0001c0002t0008g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
a0001c0002t0008g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
a0001c0002t0008g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
a0001c0002t0008g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
a0001c0003t0007g0035 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
a0001c0003t0007g0280 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
a0001c0003t0007g0281 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
a0001c0003t0007g0282 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
a0001c0003t0007g0283 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
a0001c0003t0017g0292 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
a0001c0003t0017g0293 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
a0001c0004t0004g0034 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
a0001c0004t0004g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
a0001c0004t0004g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
a0001c0004t0004g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
a0001c0004t0004g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
a0001c0005t0004g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
a0001c0005t0004g0294 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
a0001c0005t0004g0295 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
a0001c0006t0001g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
a0001c0006t0001g0018 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
a0001c0006t0001g0063 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
a0001c0008t0004g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
a0001c0008t0004g0270 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
a0001c0009t0002g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
a0001c0012t0001g0005 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
a0001c0013t0002g0001 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
a0001c0014t0006g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
a0001c0016t0004g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
a0001c0017t0001g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
a0002c0007t0002g0001 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
a0002c0007t0002g0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
a0003c0010t0002g0300 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
a0004c0011t0001g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
a0005c0015t0008g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00140 | hp1 | a0001 | c0001 | t0001 | g0125 | EUR | GBR | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
HG00140 | hp2 | a0001 | c0001 | t0002 | g0081 | EUR | GBR | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
HG00280 | hp1 | a0001 | c0001 | t0001 | g0084 | EUR | FIN | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
HG00280 | hp2 | a0001 | c0001 | t0024 | g0003 | EUR | FIN | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
HG00323 | hp1 | a0001 | c0001 | t0002 | g0001 | EUR | FIN | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
HG00323 | hp2 | a0001 | c0001 | t0001 | g0071 | EUR | FIN | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
HG00408 | hp1 | a0001 | c0002 | t0008 | g0253 | EAS | CHS | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
HG00408 | hp2 | a0001 | c0001 | t0003 | g0216 | EAS | CHS | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
HG00423 | hp1 | a0001 | c0001 | t0003 | g0003 | EAS | CHS | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
HG00423 | hp2 | a0001 | c0001 | t0002 | g0027 | EAS | CHS | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
HG00438 | hp1 | a0001 | c0001 | t0003 | g0248 | EAS | CHS | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
HG00438 | hp2 | a0001 | c0001 | t0020 | g0026 | EAS | CHS | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
HG00558 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | CHS | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
HG00558 | hp2 | a0001 | c0001 | t0001 | g0142 | EAS | CHS | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
HG00597 | hp1 | a0001 | c0001 | t0001 | g0185 | EAS | CHS | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
HG00597 | hp2 | a0001 | c0001 | t0003 | g0249 | EAS | CHS | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
HG00609 | hp1 | a0001 | c0001 | t0001 | g0009 | EAS | CHS | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
HG00609 | hp2 | a0001 | c0001 | t0003 | g0003 | EAS | CHS | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
HG00639 | hp1 | a0001 | c0001 | t0001 | g0072 | AMR | PUR | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
HG00639 | hp2 | a0001 | c0001 | t0001 | g0005 | AMR | PUR | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
HG00642 | hp1 | a0001 | c0001 | t0004 | g0002 | AMR | PUR | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
HG00642 | hp2 | a0001 | c0001 | t0003 | g0235 | AMR | PUR | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
HG00733 | hp1 | a0001 | c0001 | t0002 | g0002 | AMR | PUR | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
HG00733 | hp2 | a0001 | c0002 | t0005 | g0264 | AMR | PUR | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
HG00735 | hp1 | a0001 | c0001 | t0003 | g0246 | AMR | PUR | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
HG00735 | hp2 | a0001 | c0001 | t0001 | g0014 | AMR | PUR | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
HG00738 | hp1 | a0001 | c0001 | t0001 | g0019 | AMR | PUR | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
HG00738 | hp2 | a0001 | c0001 | t0001 | g0213 | AMR | PUR | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
HG00741 | hp1 | a0001 | c0001 | t0001 | g0019 | AMR | PUR | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
HG00741 | hp2 | a0001 | c0001 | t0002 | g0001 | AMR | PUR | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
HG01069 | hp1 | a0001 | c0001 | t0001 | g0028 | AMR | PUR | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
HG01069 | hp2 | a0001 | c0001 | t0003 | g0233 | AMR | PUR | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
HG01070 | hp1 | a0001 | c0001 | t0001 | g0299 | AMR | PUR | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
HG01070 | hp2 | a0001 | c0001 | t0002 | g0095 | AMR | PUR | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
HG01071 | hp1 | a0001 | c0001 | t0001 | g0028 | AMR | PUR | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
HG01071 | hp2 | a0001 | c0001 | t0002 | g0002 | AMR | PUR | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
HG01081 | hp1 | a0001 | c0001 | t0002 | g0002 | AMR | PUR | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
HG01081 | hp2 | a0001 | c0001 | t0001 | g0011 | AMR | PUR | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
HG01099 | hp1 | a0001 | c0001 | t0002 | g0002 | AMR | PUR | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
HG01099 | hp2 | a0001 | c0001 | t0002 | g0006 | AMR | PUR | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
HG01109 | hp1 | a0001 | c0003 | t0017 | g0292 | AMR | PUR | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
HG01109 | hp2 | a0001 | c0001 | t0001 | g0011 | AMR | PUR | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
HG01167 | hp1 | a0001 | c0003 | t0007 | g0283 | AMR | PUR | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
HG01167 | hp2 | a0001 | c0001 | t0002 | g0002 | AMR | PUR | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
HG01169 | hp1 | a0001 | c0001 | t0002 | g0002 | AMR | PUR | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
HG01169 | hp2 | a0001 | c0001 | t0001 | g0162 | AMR | PUR | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
HG01175 | hp1 | a0001 | c0001 | t0002 | g0109 | AMR | PUR | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
HG01175 | hp2 | a0001 | c0001 | t0002 | g0094 | AMR | PUR | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
HG01192 | hp1 | a0001 | c0002 | t0005 | g0263 | AMR | PUR | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
HG01192 | hp2 | a0001 | c0001 | t0006 | g0046 | AMR | PUR | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
HG01243 | hp1 | a0001 | c0001 | t0001 | g0116 | AMR | PUR | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
HG01243 | hp2 | a0001 | c0001 | t0001 | g0212 | AMR | PUR | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
HG01255 | hp1 | a0001 | c0001 | t0002 | g0092 | AMR | CLM | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
HG01255 | hp2 | a0001 | c0001 | t0003 | g0240 | AMR | CLM | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
HG01256 | hp1 | a0001 | c0001 | t0002 | g0097 | AMR | CLM | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
HG01256 | hp2 | a0001 | c0012 | t0001 | g0005 | AMR | CLM | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
HG01258 | hp1 | a0001 | c0001 | t0002 | g0096 | AMR | CLM | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
HG01258 | hp2 | a0001 | c0001 | t0001 | g0143 | AMR | CLM | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
HG01346 | hp1 | a0001 | c0001 | t0002 | g0068 | AMR | CLM | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
HG01346 | hp2 | a0001 | c0001 | t0001 | g0205 | AMR | CLM | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
HG01496 | hp1 | a0001 | c0001 | t0001 | g0005 | AMR | CLM | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
HG01496 | hp2 | a0001 | c0001 | t0002 | g0006 | AMR | CLM | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
HG01515 | hp1 | a0001 | c0001 | t0001 | g0149 | EUR | IBS | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
HG01515 | hp2 | a0001 | c0001 | t0002 | g0101 | EUR | IBS | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
HG01516 | hp1 | a0001 | c0001 | t0002 | g0061 | EUR | IBS | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
HG01516 | hp2 | a0001 | c0001 | t0003 | g0230 | EUR | IBS | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
HG01517 | hp1 | a0001 | c0001 | t0001 | g0141 | EUR | IBS | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
HG01517 | hp2 | a0001 | c0001 | t0003 | g0210 | EUR | IBS | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
HG01884 | hp1 | a0001 | c0001 | t0001 | g0121 | AFR | ACB | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
HG01884 | hp2 | a0001 | c0001 | t0004 | g0048 | AFR | ACB | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
HG01891 | hp1 | a0001 | c0001 | t0001 | g0029 | AFR | ACB | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
HG01891 | hp2 | a0001 | c0001 | t0004 | g0047 | AFR | ACB | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
HG01928 | hp1 | a0001 | c0001 | t0002 | g0067 | AMR | PEL | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
HG01928 | hp2 | a0001 | c0001 | t0001 | g0013 | AMR | PEL | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
HG01934 | hp1 | a0001 | c0001 | t0003 | g0199 | AMR | PEL | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
HG01934 | hp2 | a0001 | c0001 | t0001 | g0288 | AMR | PEL | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
HG01943 | hp1 | a0001 | c0001 | t0002 | g0065 | AMR | PEL | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
HG01943 | hp2 | a0001 | c0001 | t0001 | g0010 | AMR | PEL | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
HG01952 | hp1 | a0001 | c0001 | t0001 | g0183 | AMR | PEL | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
HG01952 | hp2 | a0001 | c0001 | t0002 | g0006 | AMR | PEL | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
HG01975 | hp1 | a0001 | c0001 | t0001 | g0128 | AMR | PEL | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
HG01975 | hp2 | a0001 | c0001 | t0002 | g0006 | AMR | PEL | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
HG01978 | hp1 | a0001 | c0001 | t0001 | g0131 | AMR | PEL | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
HG01978 | hp2 | a0001 | c0001 | t0002 | g0064 | AMR | PEL | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
HG01993 | hp1 | a0001 | c0001 | t0002 | g0066 | AMR | PEL | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
HG01993 | hp2 | a0001 | c0001 | t0001 | g0010 | AMR | PEL | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
HG02027 | hp1 | a0001 | c0002 | t0005 | g0276 | EAS | KHV | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
HG02027 | hp2 | a0001 | c0001 | t0003 | g0247 | EAS | KHV | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
HG02040 | hp1 | a0001 | c0001 | t0002 | g0007 | EAS | KHV | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
HG02040 | hp2 | a0001 | c0002 | t0005 | g0033 | EAS | KHV | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
HG02055 | hp1 | a0001 | c0001 | t0002 | g0273 | AFR | ACB | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
HG02055 | hp2 | a0001 | c0001 | t0001 | g0286 | AFR | ACB | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
HG02056 | hp1 | a0001 | c0002 | t0005 | g0256 | EAS | KHV | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
HG02056 | hp2 | a0001 | c0001 | t0011 | g0001 | EAS | KHV | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
HG02071 | hp1 | a0001 | c0001 | t0003 | g0229 | EAS | KHV | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
HG02071 | hp2 | a0001 | c0001 | t0001 | g0015 | EAS | KHV | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
HG02074 | hp1 | a0001 | c0001 | t0001 | g0009 | EAS | KHV | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
HG02074 | hp2 | a0001 | c0001 | t0002 | g0087 | EAS | KHV | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
HG02080 | hp1 | a0001 | c0001 | t0001 | g0214 | EAS | KHV | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
HG02080 | hp2 | a0001 | c0001 | t0002 | g0079 | EAS | KHV | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
HG02083 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | KHV | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
HG02083 | hp2 | a0001 | c0004 | t0004 | g0271 | EAS | KHV | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
HG02129 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | KHV | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
HG02129 | hp2 | a0001 | c0001 | t0003 | g0241 | EAS | KHV | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
HG02132 | hp1 | a0001 | c0001 | t0001 | g0158 | EAS | KHV | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
HG02132 | hp2 | a0001 | c0001 | t0002 | g0024 | EAS | KHV | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
HG02135 | hp1 | a0001 | c0001 | t0001 | g0178 | EAS | KHV | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
HG02135 | hp2 | a0001 | c0002 | t0005 | g0190 | EAS | KHV | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
HG02145 | hp1 | a0001 | c0001 | t0012 | g0302 | AFR | ACB | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
HG02145 | hp2 | a0001 | c0003 | t0007 | g0280 | AFR | ACB | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
HG02148 | hp1 | a0001 | c0001 | t0002 | g0017 | AMR | PEL | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
HG02148 | hp2 | a0001 | c0001 | t0001 | g0010 | AMR | PEL | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
HG02165 | hp1 | a0001 | c0001 | t0001 | g0147 | EAS | CDX | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
HG02165 | hp2 | a0001 | c0001 | t0003 | g0234 | EAS | CDX | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
HG02257 | hp1 | a0001 | c0001 | t0001 | g0287 | AFR | ACB | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
HG02257 | hp2 | a0001 | c0001 | t0010 | g0020 | AFR | ACB | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
HG02258 | hp1 | a0001 | c0001 | t0022 | g0005 | AFR | ACB | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
HG02258 | hp2 | a0001 | c0001 | t0001 | g0115 | AFR | ACB | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
HG02280 | hp1 | a0001 | c0001 | t0006 | g0041 | AFR | ACB | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
HG02280 | hp2 | a0001 | c0001 | t0004 | g0016 | AFR | ACB | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
HG02293 | hp1 | a0001 | c0002 | t0005 | g0089 | AMR | PEL | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
HG02293 | hp2 | a0001 | c0001 | t0001 | g0010 | AMR | PEL | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
HG02451 | hp1 | a0001 | c0001 | t0001 | g0164 | AFR | ACB | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
HG02451 | hp2 | a0001 | c0001 | t0004 | g0194 | AFR | ACB | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
HG02523 | hp1 | a0001 | c0001 | t0001 | g0186 | EAS | KHV | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
HG02523 | hp2 | a0001 | c0001 | t0003 | g0208 | EAS | KHV | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
HG02572 | hp1 | a0001 | c0001 | t0004 | g0192 | AFR | GWD | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
HG02572 | hp2 | a0001 | c0001 | t0004 | g0197 | AFR | GWD | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
HG02602 | hp1 | a0001 | c0001 | t0001 | g0004 | SAS | PJL | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
HG02602 | hp2 | a0001 | c0001 | t0002 | g0070 | SAS | PJL | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
HG02615 | hp1 | a0001 | c0001 | t0001 | g0054 | AFR | GWD | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
HG02615 | hp2 | a0001 | c0001 | t0001 | g0169 | AFR | GWD | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
HG02622 | hp1 | a0001 | c0001 | t0004 | g0016 | AFR | GWD | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
HG02622 | hp2 | a0001 | c0003 | t0007 | g0282 | AFR | GWD | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
HG02630 | hp1 | a0001 | c0001 | t0014 | g0039 | AFR | GWD | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
HG02630 | hp2 | a0001 | c0001 | t0004 | g0296 | AFR | GWD | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
HG02647 | hp1 | a0001 | c0001 | t0006 | g0037 | AFR | GWD | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
HG02647 | hp2 | a0001 | c0001 | t0006 | g0038 | AFR | GWD | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
HG02698 | hp1 | a0001 | c0001 | t0016 | g0086 | SAS | PJL | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
HG02698 | hp2 | a0001 | c0001 | t0001 | g0151 | SAS | PJL | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
HG02717 | hp1 | a0001 | c0014 | t0006 | g0043 | AFR | GWD | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
HG02717 | hp2 | a0001 | c0001 | t0026 | g0272 | AFR | GWD | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
HG02723 | hp1 | a0001 | c0001 | t0001 | g0120 | AFR | GWD | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
HG02723 | hp2 | a0001 | c0001 | t0015 | g0051 | AFR | GWD | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
HG02735 | hp1 | a0001 | c0001 | t0001 | g0005 | SAS | PJL | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
HG02735 | hp2 | a0001 | c0001 | t0002 | g0104 | SAS | PJL | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
HG02738 | hp1 | a0001 | c0001 | t0001 | g0009 | SAS | PJL | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
HG02738 | hp2 | a0001 | c0001 | t0002 | g0110 | SAS | PJL | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
HG02809 | hp1 | a0001 | c0001 | t0002 | g0001 | AFR | GWD | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
HG02809 | hp2 | a0001 | c0016 | t0004 | g0118 | AFR | GWD | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
HG02818 | hp1 | a0001 | c0001 | t0010 | g0099 | AFR | GWD | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
HG02818 | hp2 | a0001 | c0001 | t0004 | g0193 | AFR | GWD | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
HG02886 | hp1 | a0001 | c0001 | t0004 | g0030 | AFR | GWD | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
HG02886 | hp2 | a0001 | c0001 | t0004 | g0174 | AFR | GWD | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
HG02895 | hp1 | a0001 | c0001 | t0001 | g0166 | AFR | GWD | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
HG02895 | hp2 | a0001 | c0005 | t0004 | g0294 | AFR | GWD | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
HG02896 | hp1 | a0001 | c0001 | t0004 | g0176 | AFR | GWD | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
HG02896 | hp2 | a0001 | c0001 | t0001 | g0163 | AFR | GWD | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
HG02897 | hp1 | a0001 | c0001 | t0004 | g0129 | AFR | GWD | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
HG02897 | hp2 | a0001 | c0001 | t0001 | g0167 | AFR | GWD | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
HG02922 | hp1 | a0001 | c0001 | t0001 | g0119 | AFR | ESN | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
HG02922 | hp2 | a0001 | c0001 | t0004 | g0030 | AFR | ESN | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
HG02965 | hp1 | a0001 | c0001 | t0004 | g0284 | AFR | ESN | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
HG02965 | hp2 | a0002 | c0007 | t0002 | g0007 | AFR | ESN | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
HG02970 | hp1 | a0001 | c0001 | t0006 | g0040 | AFR | ESN | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
HG02970 | hp2 | a0001 | c0001 | t0013 | g0032 | AFR | ESN | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
HG02976 | hp1 | a0001 | c0001 | t0012 | g0036 | AFR | ESN | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
HG02976 | hp2 | a0001 | c0001 | t0004 | g0191 | AFR | ESN | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
HG03017 | hp1 | a0001 | c0001 | t0001 | g0157 | SAS | PJL | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
HG03017 | hp2 | a0001 | c0002 | t0005 | g0259 | SAS | PJL | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
HG03041 | hp1 | a0001 | c0001 | t0001 | g0076 | AFR | GWD | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
HG03041 | hp2 | a0001 | c0001 | t0001 | g0173 | AFR | GWD | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
HG03098 | hp1 | a0001 | c0003 | t0007 | g0035 | AFR | MSL | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
HG03098 | hp2 | a0001 | c0001 | t0001 | g0114 | AFR | MSL | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
HG03130 | hp1 | a0001 | c0001 | t0001 | g0117 | AFR | ESN | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
HG03130 | hp2 | a0001 | c0001 | t0014 | g0042 | AFR | ESN | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
HG03139 | hp1 | a0001 | c0001 | t0001 | g0171 | AFR | ESN | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
HG03139 | hp2 | a0001 | c0001 | t0001 | g0170 | AFR | ESN | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
HG03195 | hp1 | a0001 | c0001 | t0010 | g0020 | AFR | ESN | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
HG03195 | hp2 | a0001 | c0005 | t0004 | g0295 | AFR | ESN | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
HG03209 | hp1 | a0001 | c0001 | t0014 | g0045 | AFR | MSL | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
HG03209 | hp2 | a0001 | c0001 | t0013 | g0251 | AFR | MSL | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
HG03239 | hp1 | a0001 | c0001 | t0002 | g0024 | SAS | PJL | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
HG03239 | hp2 | a0001 | c0001 | t0018 | g0106 | SAS | PJL | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
HG03453 | hp1 | a0002 | c0007 | t0002 | g0001 | AFR | MSL | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
HG03453 | hp2 | a0001 | c0001 | t0027 | g0052 | AFR | MSL | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
HG03486 | hp1 | a0001 | c0001 | t0001 | g0187 | AFR | MSL | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
HG03486 | hp2 | a0001 | c0003 | t0017 | g0293 | AFR | MSL | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
HG03490 | hp1 | a0001 | c0001 | t0002 | g0025 | SAS | PJL | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
HG03490 | hp2 | a0001 | c0001 | t0001 | g0126 | SAS | PJL | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
HG03491 | hp1 | a0001 | c0001 | t0001 | g0290 | SAS | PJL | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
HG03491 | hp2 | a0001 | c0001 | t0003 | g0123 | SAS | PJL | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
HG03492 | hp1 | a0001 | c0001 | t0003 | g0124 | SAS | PJL | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
HG03492 | hp2 | a0001 | c0001 | t0002 | g0025 | SAS | PJL | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
HG03516 | hp1 | a0001 | c0001 | t0004 | g0297 | AFR | ESN | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
HG03516 | hp2 | a0001 | c0001 | t0013 | g0032 | AFR | ESN | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
HG03540 | hp1 | a0001 | c0003 | t0007 | g0035 | AFR | GWD | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
HG03540 | hp2 | a0001 | c0001 | t0001 | g0225 | AFR | GWD | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
HG03579 | hp1 | a0001 | c0001 | t0004 | g0196 | AFR | MSL | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
HG03579 | hp2 | a0001 | c0001 | t0004 | g0298 | AFR | MSL | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
HG03654 | hp1 | a0001 | c0001 | t0003 | g0231 | SAS | PJL | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
HG03654 | hp2 | a0001 | c0002 | t0005 | g0257 | SAS | PJL | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
HG03669 | hp1 | a0001 | c0002 | t0005 | g0255 | SAS | PJL | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
HG03669 | hp2 | a0001 | c0001 | t0001 | g0161 | SAS | PJL | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
HG03688 | hp1 | a0001 | c0001 | t0003 | g0227 | SAS | STU | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
HG03688 | hp2 | a0001 | c0002 | t0005 | g0254 | SAS | STU | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
HG03704 | hp1 | a0001 | c0001 | t0002 | g0056 | SAS | PJL | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
HG03704 | hp2 | a0001 | c0001 | t0003 | g0155 | SAS | PJL | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
HG03710 | hp1 | a0001 | c0001 | t0019 | g0107 | SAS | PJL | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
HG03710 | hp2 | a0001 | c0001 | t0003 | g0209 | SAS | PJL | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
HG03831 | hp1 | a0001 | c0001 | t0003 | g0202 | SAS | BEB | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
HG03831 | hp2 | a0001 | c0001 | t0001 | g0127 | SAS | BEB | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
HG03834 | hp1 | a0001 | c0001 | t0001 | g0093 | SAS | BEB | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
HG03834 | hp2 | a0001 | c0002 | t0005 | g0252 | SAS | BEB | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
HG03927 | hp1 | a0001 | c0001 | t0003 | g0275 | SAS | BEB | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
HG03927 | hp2 | a0001 | c0001 | t0002 | g0103 | SAS | BEB | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
HG03942 | hp1 | a0001 | c0001 | t0001 | g0018 | SAS | BEB | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
HG03942 | hp2 | a0001 | c0001 | t0016 | g0088 | SAS | BEB | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
HG04184 | hp1 | a0001 | c0001 | t0003 | g0291 | SAS | BEB | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
HG04184 | hp2 | a0001 | c0001 | t0003 | g0189 | SAS | BEB | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
HG04199 | hp1 | a0001 | c0001 | t0003 | g0221 | SAS | STU | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
HG04199 | hp2 | a0001 | c0001 | t0001 | g0203 | SAS | STU | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
HG04204 | hp1 | a0001 | c0001 | t0001 | g0138 | SAS | STU | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
HG04204 | hp2 | a0001 | c0001 | t0001 | g0074 | SAS | STU | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
HG04228 | hp1 | a0001 | c0001 | t0001 | g0004 | SAS | STU | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
HG04228 | hp2 | a0001 | c0008 | t0004 | g0270 | SAS | STU | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
NA18522 | hp1 | a0001 | c0001 | t0004 | g0016 | AFR | YRI | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
NA18522 | hp2 | a0001 | c0001 | t0015 | g0050 | AFR | YRI | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
NA18612 | hp1 | a0001 | c0001 | t0002 | g0007 | EAS | CHB | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
NA18612 | hp2 | a0001 | c0001 | t0003 | g0003 | EAS | CHB | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
NA18906 | hp1 | a0001 | c0001 | t0004 | g0172 | AFR | YRI | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
NA18906 | hp2 | a0001 | c0002 | t0005 | g0055 | AFR | YRI | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
NA18939 | hp1 | a0001 | c0001 | t0002 | g0075 | EAS | JPT | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
NA18939 | hp2 | a0001 | c0017 | t0001 | g0049 | EAS | JPT | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
NA18940 | hp1 | a0001 | c0001 | t0002 | g0059 | EAS | JPT | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
NA18940 | hp2 | a0001 | c0001 | t0001 | g0215 | EAS | JPT | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
NA18942 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
NA18942 | hp2 | a0001 | c0001 | t0003 | g0285 | EAS | JPT | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
NA18943 | hp1 | a0001 | c0001 | t0002 | g0026 | EAS | JPT | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
NA18943 | hp2 | a0001 | c0001 | t0001 | g0207 | EAS | JPT | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
NA18945 | hp1 | a0001 | c0001 | t0002 | g0058 | EAS | JPT | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
NA18945 | hp2 | a0001 | c0001 | t0002 | g0021 | EAS | JPT | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
NA18946 | hp1 | a0001 | c0001 | t0009 | g0031 | EAS | JPT | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
NA18946 | hp2 | a0001 | c0001 | t0001 | g0136 | EAS | JPT | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
NA18947 | hp1 | a0001 | c0001 | t0002 | g0085 | EAS | JPT | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
NA18947 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
NA18951 | hp1 | a0001 | c0001 | t0001 | g0132 | EAS | JPT | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
NA18951 | hp2 | a0001 | c0001 | t0002 | g0057 | EAS | JPT | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
NA18952 | hp1 | a0001 | c0001 | t0009 | g0150 | EAS | JPT | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
NA18952 | hp2 | a0001 | c0004 | t0004 | g0034 | EAS | JPT | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
NA18953 | hp1 | a0001 | c0001 | t0023 | g0204 | EAS | JPT | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
NA18953 | hp2 | a0001 | c0001 | t0002 | g0023 | EAS | JPT | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
NA18957 | hp1 | a0001 | c0001 | t0003 | g0226 | EAS | JPT | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
NA18957 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
NA18959 | hp1 | a0001 | c0001 | t0002 | g0105 | EAS | JPT | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
NA18959 | hp2 | a0001 | c0001 | t0001 | g0139 | EAS | JPT | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
NA18960 | hp1 | a0001 | c0001 | t0001 | g0137 | EAS | JPT | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
NA18960 | hp2 | a0001 | c0001 | t0003 | g0003 | EAS | JPT | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
NA18961 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
NA18961 | hp2 | a0001 | c0001 | t0003 | g0244 | EAS | JPT | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
NA18962 | hp1 | a0001 | c0001 | t0004 | g0007 | EAS | JPT | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
NA18962 | hp2 | a0001 | c0001 | t0003 | g0239 | EAS | JPT | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
NA18963 | hp1 | a0001 | c0001 | t0003 | g0198 | EAS | JPT | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
NA18963 | hp2 | a0001 | c0001 | t0001 | g0206 | EAS | JPT | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
NA18967 | hp1 | a0001 | c0001 | t0003 | g0218 | EAS | JPT | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
NA18967 | hp2 | a0001 | c0004 | t0004 | g0269 | EAS | JPT | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
NA18969 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
NA18969 | hp2 | a0001 | c0001 | t0002 | g0022 | EAS | JPT | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
NA18970 | hp1 | a0001 | c0004 | t0004 | g0265 | EAS | JPT | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
NA18970 | hp2 | a0001 | c0001 | t0003 | g0224 | EAS | JPT | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
NA18972 | hp1 | a0001 | c0001 | t0001 | g0134 | EAS | JPT | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
NA18972 | hp2 | a0001 | c0001 | t0002 | g0023 | EAS | JPT | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
NA18973 | hp1 | a0001 | c0001 | t0003 | g0201 | EAS | JPT | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
NA18973 | hp2 | a0001 | c0002 | t0008 | g0261 | EAS | JPT | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
NA18975 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
NA18975 | hp2 | a0001 | c0001 | t0001 | g0160 | EAS | JPT | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
NA18977 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
NA18977 | hp2 | a0001 | c0002 | t0005 | g0279 | EAS | JPT | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
NA18978 | hp1 | a0001 | c0001 | t0021 | g0184 | EAS | JPT | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
NA18978 | hp2 | a0001 | c0001 | t0003 | g0003 | EAS | JPT | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
NA18980 | hp1 | a0001 | c0001 | t0001 | g0130 | EAS | JPT | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
NA18980 | hp2 | a0001 | c0001 | t0002 | g0090 | EAS | JPT | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
NA18981 | hp1 | a0001 | c0001 | t0002 | g0060 | EAS | JPT | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
NA18981 | hp2 | a0001 | c0001 | t0003 | g0250 | EAS | JPT | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
NA18985 | hp1 | a0001 | c0001 | t0003 | g0274 | EAS | JPT | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
NA18985 | hp2 | a0001 | c0002 | t0005 | g0260 | EAS | JPT | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
NA18986 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
NA18986 | hp2 | a0001 | c0001 | t0001 | g0113 | EAS | JPT | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
NA18989 | hp1 | a0001 | c0001 | t0001 | g0156 | EAS | JPT | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
NA18989 | hp2 | a0001 | c0001 | t0002 | g0078 | EAS | JPT | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
NA18990 | hp1 | a0001 | c0004 | t0004 | g0034 | EAS | JPT | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
NA18990 | hp2 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
NA18991 | hp1 | a0001 | c0001 | t0009 | g0228 | EAS | JPT | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
NA18991 | hp2 | a0001 | c0001 | t0003 | g0200 | EAS | JPT | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
NA18993 | hp1 | a0001 | c0001 | t0011 | g0008 | EAS | JPT | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
NA18993 | hp2 | a0004 | c0011 | t0001 | g0180 | EAS | JPT | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
NA18994 | hp1 | a0001 | c0001 | t0002 | g0069 | EAS | JPT | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
NA18994 | hp2 | a0001 | c0008 | t0004 | g0268 | EAS | JPT | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
NA18995 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
NA18995 | hp2 | a0001 | c0001 | t0002 | g0082 | EAS | JPT | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
NA18998 | hp1 | a0001 | c0001 | t0003 | g0243 | EAS | JPT | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
NA18998 | hp2 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
NA19000 | hp1 | a0001 | c0001 | t0002 | g0012 | EAS | JPT | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
NA19000 | hp2 | a0001 | c0001 | t0003 | g0303 | EAS | JPT | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
NA19002 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
NA19002 | hp2 | a0001 | c0001 | t0003 | g0217 | EAS | JPT | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
NA19003 | hp1 | a0001 | c0001 | t0003 | g0219 | EAS | JPT | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
NA19003 | hp2 | a0001 | c0001 | t0002 | g0083 | EAS | JPT | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
NA19005 | hp1 | a0001 | c0001 | t0001 | g0153 | EAS | JPT | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
NA19005 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
NA19007 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
NA19007 | hp2 | a0001 | c0001 | t0001 | g0181 | EAS | JPT | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
NA19009 | hp1 | a0001 | c0001 | t0001 | g0146 | EAS | JPT | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
NA19009 | hp2 | a0001 | c0001 | t0004 | g0012 | EAS | JPT | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
NA19010 | hp1 | a0001 | c0002 | t0005 | g0033 | EAS | JPT | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
NA19010 | hp2 | a0001 | c0001 | t0002 | g0108 | EAS | JPT | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
NA19011 | hp1 | a0001 | c0001 | t0003 | g0220 | EAS | JPT | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
NA19011 | hp2 | a0001 | c0001 | t0002 | g0012 | EAS | JPT | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
NA19012 | hp1 | a0001 | c0001 | t0003 | g0003 | EAS | JPT | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
NA19012 | hp2 | a0001 | c0001 | t0002 | g0022 | EAS | JPT | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
NA19030 | hp1 | a0001 | c0001 | t0001 | g0165 | AFR | LWK | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
NA19030 | hp2 | a0001 | c0001 | t0006 | g0044 | AFR | LWK | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
NA19054 | hp1 | a0001 | c0001 | t0002 | g0027 | EAS | JPT | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
NA19054 | hp2 | a0001 | c0001 | t0003 | g0236 | EAS | JPT | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
NA19056 | hp1 | a0001 | c0001 | t0003 | g0223 | EAS | JPT | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
NA19056 | hp2 | a0001 | c0001 | t0001 | g0177 | EAS | JPT | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
NA19057 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
NA19057 | hp2 | a0001 | c0001 | t0003 | g0242 | EAS | JPT | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
NA19058 | hp1 | a0001 | c0001 | t0001 | g0133 | EAS | JPT | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
NA19058 | hp2 | a0001 | c0002 | t0008 | g0278 | EAS | JPT | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
NA19060 | hp1 | a0001 | c0001 | t0002 | g0111 | EAS | JPT | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
NA19060 | hp2 | a0001 | c0001 | t0003 | g0222 | EAS | JPT | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
NA19062 | hp1 | a0001 | c0001 | t0002 | g0091 | EAS | JPT | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
NA19062 | hp2 | a0001 | c0001 | t0003 | g0211 | EAS | JPT | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
NA19063 | hp1 | a0001 | c0001 | t0001 | g0159 | EAS | JPT | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
NA19063 | hp2 | a0001 | c0001 | t0002 | g0021 | EAS | JPT | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
NA19064 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
NA19064 | hp2 | a0001 | c0001 | t0003 | g0232 | EAS | JPT | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
NA19065 | hp1 | a0001 | c0001 | t0001 | g0237 | EAS | JPT | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
NA19065 | hp2 | a0001 | c0001 | t0001 | g0152 | EAS | JPT | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
NA19067 | hp1 | a0001 | c0001 | t0002 | g0289 | EAS | JPT | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
NA19067 | hp2 | a0001 | c0001 | t0003 | g0238 | EAS | JPT | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
NA19068 | hp1 | a0001 | c0002 | t0008 | g0262 | EAS | JPT | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
NA19068 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
NA19070 | hp1 | a0001 | c0001 | t0001 | g0148 | EAS | JPT | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
NA19070 | hp2 | a0001 | c0001 | t0002 | g0008 | EAS | JPT | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
NA19074 | hp1 | a0001 | c0001 | t0001 | g0154 | EAS | JPT | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
NA19074 | hp2 | a0001 | c0001 | t0011 | g0001 | EAS | JPT | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
NA19080 | hp1 | a0005 | c0015 | t0008 | g0258 | EAS | JPT | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
NA19080 | hp2 | a0001 | c0001 | t0001 | g0015 | EAS | JPT | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
NA19082 | hp1 | a0001 | c0013 | t0002 | g0001 | EAS | JPT | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
NA19082 | hp2 | a0001 | c0004 | t0004 | g0267 | EAS | JPT | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
NA19083 | hp1 | a0001 | c0001 | t0009 | g0140 | EAS | JPT | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
NA19083 | hp2 | a0001 | c0001 | t0002 | g0080 | EAS | JPT | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
NA19084 | hp1 | a0001 | c0001 | t0001 | g0144 | EAS | JPT | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
NA19084 | hp2 | a0001 | c0001 | t0003 | g0003 | EAS | JPT | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
NA19085 | hp1 | a0001 | c0001 | t0002 | g0008 | EAS | JPT | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
NA19085 | hp2 | a0001 | c0001 | t0003 | g0245 | EAS | JPT | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
NA19087 | hp1 | a0001 | c0001 | t0001 | g0182 | EAS | JPT | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
NA19087 | hp2 | a0001 | c0001 | t0003 | g0031 | EAS | JPT | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
NA19088 | hp1 | a0001 | c0001 | t0001 | g0015 | EAS | JPT | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
NA19088 | hp2 | a0001 | c0001 | t0003 | g0188 | EAS | JPT | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
NA19089 | hp1 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
NA19089 | hp2 | a0001 | c0002 | t0008 | g0277 | EAS | JPT | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
NA19090 | hp1 | a0001 | c0001 | t0001 | g0179 | EAS | JPT | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
NA19090 | hp2 | a0001 | c0009 | t0002 | g0266 | EAS | JPT | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
NA19091 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
NA19091 | hp2 | a0001 | c0001 | t0001 | g0135 | EAS | JPT | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
NA19240 | hp1 | a0001 | c0001 | t0001 | g0029 | AFR | YRI | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
NA19240 | hp2 | a0001 | c0001 | t0004 | g0100 | AFR | YRI | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
NA20752 | hp1 | a0001 | c0001 | t0002 | g0098 | EUR | TSI | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
NA20752 | hp2 | a0001 | c0001 | t0001 | g0013 | EUR | TSI | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
NA20905 | hp1 | a0001 | c0001 | t0001 | g0145 | SAS | GIH | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
NA20905 | hp2 | a0001 | c0006 | t0001 | g0018 | SAS | GIH | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
HG01123 | hp1 | a0001 | c0001 | t0001 | g0073 | AMR | CLM | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
HG01123 | hp2 | a0001 | c0001 | t0002 | g0017 | AMR | CLM | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
HG02109 | hp1 | a0001 | c0001 | t0001 | g0168 | AFR | ACB | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
HG02109 | hp2 | a0001 | c0001 | t0012 | g0036 | AFR | ACB | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
HG02486 | hp1 | a0001 | c0006 | t0001 | g0014 | AFR | ACB | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
HG02486 | hp2 | a0001 | c0001 | t0001 | g0062 | AFR | ACB | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
HG02559 | hp1 | a0001 | c0001 | t0015 | g0053 | AFR | ACB | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
HG02559 | hp2 | a0001 | c0001 | t0025 | g0301 | AFR | ACB | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
HG03471 | hp1 | a0001 | c0005 | t0004 | g0122 | AFR | MSL | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
HG03471 | hp2 | a0001 | c0001 | t0004 | g0195 | AFR | MSL | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
HG06807 | hp1 | a0003 | c0010 | t0002 | g0300 | AFR | USA | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
HG06807 | hp2 | a0001 | c0003 | t0007 | g0281 | AFR | USA | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
NA18955 | hp1 | a0001 | c0001 | t0002 | g0102 | EAS | JPT | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
NA18955 | hp2 | a0001 | c0001 | t0001 | g0014 | EAS | JPT | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
NA20300 | hp1 | a0001 | c0001 | t0001 | g0011 | AFR | USA | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
NA20300 | hp2 | a0001 | c0001 | t0002 | g0002 | AFR | USA | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
NA21309 | hp1 | a0001 | c0001 | t0004 | g0175 | AFR | LWK | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
NA21309 | hp2 | a0001 | c0001 | t0002 | g0112 | AFR | LWK | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
homoSapiens_chm13v2 | hp1 | a0001 | c0006 | t0001 | g0063 | REF | REF | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
homoSapiens_grch38 | hp1 | a0001 | c0001 | t0002 | g0077 | REF | REF | MFN2_chr1_11975444_12018508 | MFN2 | chr1 | 11975444 | 12018508 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr1:12002088
|
C | T | 1 | a0005 | 1 | NA19080.hp1 | missense_variant | MODERATE | c.1145C>T | p.Ala382Val | MFN2 | ENSG00000116688.18 | transcript | ENST00000235329.10 | protein_coding | 11/19 | 1335/4407 | 1145/2274 | 382/757 | chr1 | 12002088 | ||
chr1:12004010
|
G | A | 1 | a0002 | 2 | HG02965.hp2 HG03453.hp1 |
missense_variant | MODERATE | c.1179G>A | p.Met393Ile | MFN2 | ENSG00000116688.18 | transcript | ENST00000235329.10 | protein_coding | 12/19 | 1369/4407 | 1179/2274 | 393/757 | chr1 | 12004010 | ||
chr1:12004030
|
G | A | 1 | a0003 | 1 | HG06807.hp1 | missense_variant | MODERATE | c.1199G>A | p.Arg400Gln | MFN2 | ENSG00000116688.18 | transcript | ENST00000235329.10 | protein_coding | 12/19 | 1389/4407 | 1199/2274 | 400/757 | chr1 | 12004030 | ||
chr1:12004923
|
G | A | 1 | a0004 | 1 | NA18993.hp2 | missense_variant | MODERATE | c.1491G>A | p.Met497Ile | MFN2 | ENSG00000116688.18 | transcript | ENST00000235329.10 | protein_coding | 14/19 | 1681/4407 | 1491/2274 | 497/757 | chr1 | 12004923 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr1:11989318
|
C | A | 2 | a0001c0004a0001c0009 | 7 | HG02083.hp2 NA18952.hp2 NA18967.hp2 others(4): Show |
synonymous_variant | LOW | c.150C>A | p.Ile50Ile | MFN2 | ENSG00000116688.18 | transcript | ENST00000235329.10 | protein_coding | 3/19 | 340/4407 | 150/2274 | 50/757 | chr1 | 11989318 | ||
chr1:11989327
|
C | T | 1 | a0001c0003 | 8 | HG01109.hp1 HG01167.hp1 HG02145.hp2 others(5): Show |
synonymous_variant | LOW | c.159C>T | p.Ser53Ser | MFN2 | ENSG00000116688.18 | transcript | ENST00000235329.10 | protein_coding | 3/19 | 349/4407 | 159/2274 | 53/757 | chr1 | 11989327 | ||
chr1:11989333
|
C | T | 3 | a0001c0004a0001c0008a0001c0009 | 9 | HG02083.hp2 HG04228.hp2 NA18952.hp2 others(6): Show |
synonymous_variant | LOW | c.165C>T | p.Thr55Thr | MFN2 | ENSG00000116688.18 | transcript | ENST00000235329.10 | protein_coding | 3/19 | 355/4407 | 165/2274 | 55/757 | chr1 | 11989333 | ||
chr1:11996225
|
C | T | 1 | a0001c0017 | 1 | NA18939.hp2 | synonymous_variant | LOW | c.381C>T | p.Gly127Gly | MFN2 | ENSG00000116688.18 | transcript | ENST00000235329.10 | protein_coding | 5/19 | 571/4407 | 381/2274 | 127/757 | chr1 | 11996225 | ||
chr1:11996252
|
A | T | 3 | a0001c0004a0001c0008a0001c0009 | 9 | HG02083.hp2 HG04228.hp2 NA18952.hp2 others(6): Show |
synonymous_variant | LOW | c.408A>T | p.Val136Val | MFN2 | ENSG00000116688.18 | transcript | ENST00000235329.10 | protein_coding | 5/19 | 598/4407 | 408/2274 | 136/757 | chr1 | 11996252 | ||
chr1:11999023
|
C | T | 1 | a0001c0016 | 1 | HG02809.hp2 | synonymous_variant | LOW | c.744C>T | p.Leu248Leu | MFN2 | ENSG00000116688.18 | transcript | ENST00000235329.10 | protein_coding | 8/19 | 934/4407 | 744/2274 | 248/757 | chr1 | 11999023 | ||
chr1:12001541
|
C | T | 1 | a0001c0006 | 3 | HG02486.hp1 NA20905.hp2 homoSapiens_chm13v2.hp1 |
synonymous_variant | LOW | c.957C>T | p.Gly319Gly | MFN2 | ENSG00000116688.18 | transcript | ENST00000235329.10 | protein_coding | 9/19 | 1147/4407 | 957/2274 | 319/757 | chr1 | 12001541 | ||
chr1:12001773
|
C | T | 1 | a0001c0005 | 3 | HG02895.hp2 HG03195.hp2 HG03471.hp1 |
synonymous_variant | LOW | c.975C>T | p.Gly325Gly | MFN2 | ENSG00000116688.18 | transcript | ENST00000235329.10 | protein_coding | 10/19 | 1165/4407 | 975/2274 | 325/757 | chr1 | 12001773 | ||
chr1:12005784
|
C | T | 4 | a0001c0002a0001c0004a0001c0008others(1): Show | 30 | HG00408.hp1 HG00733.hp2 HG01192.hp1 others(27): Show |
synonymous_variant | LOW | c.1569C>T | p.Ser523Ser | MFN2 | ENSG00000116688.18 | transcript | ENST00000235329.10 | protein_coding | 15/19 | 1759/4407 | 1569/2274 | 523/757 | chr1 | 12005784 | ||
chr1:12006549
|
C | T | 1 | a0001c0014 | 1 | HG02717.hp1 | synonymous_variant | LOW | c.1728C>T | p.Pro576Pro | MFN2 | ENSG00000116688.18 | transcript | ENST00000235329.10 | protein_coding | 16/19 | 1918/4407 | 1728/2274 | 576/757 | chr1 | 12006549 | ||
chr1:12006567
|
C | G | 1 | a0001c0013 | 1 | NA19082.hp1 | synonymous_variant | LOW | c.1746C>G | p.Ala582Ala | MFN2 | ENSG00000116688.18 | transcript | ENST00000235329.10 | protein_coding | 16/19 | 1936/4407 | 1746/2274 | 582/757 | chr1 | 12006567 | ||
chr1:12007100
|
C | G | 1 | a0001c0012 | 1 | HG01256.hp2 | synonymous_variant | LOW | c.1920C>G | p.Leu640Leu | MFN2 | ENSG00000116688.18 | transcript | ENST00000235329.10 | protein_coding | 17/19 | 2110/4407 | 1920/2274 | 640/757 | chr1 | 12007100 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr1:11982039
|
C | T | 2 | a0001c0001t0015a0001c0001t0027 | 4 | HG02559.hp1 HG02723.hp2 HG03453.hp2 others(1): Show |
5_prime_UTR_variant | MODIFIER | c.-80C>T | MFN2 | ENSG00000116688.18 | transcript | ENST00000235329.10 | protein_coding | 2/19 | 7130 | chr1 | 11982039 | |||||
chr1:12011579
|
C | T | 1 | a0001c0001t0027 | 1 | HG03453.hp2 | 3_prime_UTR_variant | MODIFIER | c.*14C>T | MFN2 | ENSG00000116688.18 | transcript | ENST00000235329.10 | protein_coding | 19/19 | 14 | chr1 | 12011579 | |||||
chr1:12011623
|
A | G | 30 | a0001c0001t0001a0001c0001t0003a0001c0001t0004others(27): Show | 287 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(284): Show |
3_prime_UTR_variant | MODIFIER | c.*58A>G | MFN2 | ENSG00000116688.18 | transcript | ENST00000235329.10 | protein_coding | 19/19 | 58 | chr1 | 12011623 | |||||
chr1:12011656
|
G | C | 1 | a0001c0001t0021 | 1 | NA18978.hp1 | 3_prime_UTR_variant | MODIFIER | c.*91G>C | MFN2 | ENSG00000116688.18 | transcript | ENST00000235329.10 | protein_coding | 19/19 | 91 | chr1 | 12011656 | |||||
chr1:12011784
|
C | CTT | 2 | a0001c0001t0011a0001c0001t0020 | 4 | HG00438.hp2 HG02056.hp2 NA18993.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*221_*222dupTT | MFN2 | ENSG00000116688.18 | transcript | ENST00000235329.10 | protein_coding | 19/19 | 223 | INFO_REALIGN_3_PRIME | chr1 | 12011784 | ||||
chr1:12011796
|
G | A | 2 | a0001c0001t0012a0001c0001t0013 | 6 | HG02109.hp2 HG02145.hp1 HG02970.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*231G>A | MFN2 | ENSG00000116688.18 | transcript | ENST00000235329.10 | protein_coding | 19/19 | 231 | chr1 | 12011796 | |||||
chr1:12011815
|
C | G | 1 | a0001c0001t0026 | 1 | HG02717.hp2 | 3_prime_UTR_variant | MODIFIER | c.*250C>G | MFN2 | ENSG00000116688.18 | transcript | ENST00000235329.10 | protein_coding | 19/19 | 250 | chr1 | 12011815 | |||||
chr1:12011869
|
A | G | 1 | a0001c0001t0013 | 3 | HG02970.hp2 HG03209.hp2 HG03516.hp2 |
3_prime_UTR_variant | MODIFIER | c.*304A>G | MFN2 | ENSG00000116688.18 | transcript | ENST00000235329.10 | protein_coding | 19/19 | 304 | chr1 | 12011869 | |||||
chr1:12012295
|
C | T | 3 | a0001c0001t0006a0001c0001t0025a0001c0014t0006 | 8 | HG01192.hp2 HG02280.hp1 HG02559.hp2 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*730C>T | MFN2 | ENSG00000116688.18 | transcript | ENST00000235329.10 | protein_coding | 19/19 | 730 | chr1 | 12012295 | |||||
chr1:12012342
|
T | C | 1 | a0001c0003t0007 | 6 | HG01167.hp1 HG02145.hp2 HG02622.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*777T>C | MFN2 | ENSG00000116688.18 | transcript | ENST00000235329.10 | protein_coding | 19/19 | 777 | chr1 | 12012342 | |||||
chr1:12012461
|
G | C | 16 | a0001c0001t0001a0001c0001t0003a0001c0001t0009others(13): Show | 214 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(211): Show |
3_prime_UTR_variant | MODIFIER | c.*896G>C | MFN2 | ENSG00000116688.18 | transcript | ENST00000235329.10 | protein_coding | 19/19 | 896 | chr1 | 12012461 | |||||
chr1:12012477
|
C | T | 3 | a0001c0001t0003a0001c0001t0009a0001c0001t0024 | 64 | HG00280.hp2 HG00408.hp2 HG00423.hp1 others(61): Show |
3_prime_UTR_variant | MODIFIER | c.*912C>T | MFN2 | ENSG00000116688.18 | transcript | ENST00000235329.10 | protein_coding | 19/19 | 912 | chr1 | 12012477 | |||||
chr1:12012599
|
C | T | 1 | a0001c0001t0010 | 3 | HG02257.hp2 HG02818.hp1 HG03195.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1034C>T | MFN2 | ENSG00000116688.18 | transcript | ENST00000235329.10 | protein_coding | 19/19 | 1034 | chr1 | 12012599 | |||||
chr1:12012624
|
A | G | 1 | a0001c0001t0019 | 1 | HG03710.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1059A>G | MFN2 | ENSG00000116688.18 | transcript | ENST00000235329.10 | protein_coding | 19/19 | 1059 | chr1 | 12012624 | |||||
chr1:12012665
|
A | G | 6 | a0001c0001t0016a0001c0001t0019a0001c0001t0024others(3): Show | 26 | HG00280.hp2 HG00408.hp1 HG00733.hp2 others(23): Show |
3_prime_UTR_variant | MODIFIER | c.*1100A>G | MFN2 | ENSG00000116688.18 | transcript | ENST00000235329.10 | protein_coding | 19/19 | 1100 | chr1 | 12012665 | |||||
chr1:12012726
|
C | A | 1 | a0001c0003t0007 | 6 | HG01167.hp1 HG02145.hp2 HG02622.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*1161C>A | MFN2 | ENSG00000116688.18 | transcript | ENST00000235329.10 | protein_coding | 19/19 | 1161 | chr1 | 12012726 | |||||
chr1:12012875
|
G | A | 1 | a0001c0001t0026 | 1 | HG02717.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1310G>A | MFN2 | ENSG00000116688.18 | transcript | ENST00000235329.10 | protein_coding | 19/19 | 1310 | chr1 | 12012875 | |||||
chr1:12012900
|
C | T | 1 | a0001c0001t0025 | 1 | HG02559.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1335C>T | MFN2 | ENSG00000116688.18 | transcript | ENST00000235329.10 | protein_coding | 19/19 | 1335 | chr1 | 12012900 | |||||
chr1:12013104
|
G | A | 1 | a0001c0001t0022 | 1 | HG02258.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1539G>A | MFN2 | ENSG00000116688.18 | transcript | ENST00000235329.10 | protein_coding | 19/19 | 1539 | chr1 | 12013104 | |||||
chr1:12013127
|
G | A | 1 | a0001c0001t0018 | 1 | HG03239.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1562G>A | MFN2 | ENSG00000116688.18 | transcript | ENST00000235329.10 | protein_coding | 19/19 | 1562 | chr1 | 12013127 | |||||
chr1:12013141
|
C | T | 3 | a0001c0001t0006a0001c0001t0014a0001c0014t0006 | 10 | HG01192.hp2 HG02280.hp1 HG02630.hp1 others(7): Show |
3_prime_UTR_variant | MODIFIER | c.*1576C>T | MFN2 | ENSG00000116688.18 | transcript | ENST00000235329.10 | protein_coding | 19/19 | 1576 | chr1 | 12013141 | |||||
chr1:12013194
|
G | GA | 3 | a0001c0001t0023a0001c0003t0007a0001c0003t0017 | 9 | HG01109.hp1 HG01167.hp1 HG02145.hp2 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*1640dupA | MFN2 | ENSG00000116688.18 | transcript | ENST00000235329.10 | protein_coding | 19/19 | 1641 | INFO_REALIGN_3_PRIME | chr1 | 12013194 | ||||
chr1:12013359
|
ATTG | A | 2 | a0001c0001t0011a0001c0001t0020 | 4 | HG00438.hp2 HG02056.hp2 NA18993.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*1800_*1802delGTT | MFN2 | ENSG00000116688.18 | transcript | ENST00000235329.10 | protein_coding | 19/19 | 1800 | INFO_REALIGN_3_PRIME | chr1 | 12013359 | ||||
chr1:12013395
|
C | T | 1 | a0001c0001t0009 | 4 | NA18946.hp1 NA18952.hp1 NA18991.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*1830C>T | MFN2 | ENSG00000116688.18 | transcript | ENST00000235329.10 | protein_coding | 19/19 | 1830 | chr1 | 12013395 | |||||
chr1:12013431
|
G | C | 1 | a0001c0001t0020 | 1 | HG00438.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1866G>C | MFN2 | ENSG00000116688.18 | transcript | ENST00000235329.10 | protein_coding | 19/19 | 1866 | chr1 | 12013431 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr1:11980585
|
G | A | 11 | a0001c0001t0004g0047a0001c0001t0006g0037a0001c0001t0006g0038others(8): Show | 11 | HG01192.hp2 HG01891.hp2 HG02280.hp1 others(8): Show |
intron_variant | MODIFIER | c.-150+101G>A | MFN2 | ENSG00000116688.18 | transcript | ENST00000235329.10 | protein_coding | 1/18 | chr1 | 11980585 | ||||||
chr1:11980621
|
G | A | 1 | a0001c0001t0004g0048 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.-150+137G>A | MFN2 | ENSG00000116688.18 | transcript | ENST00000235329.10 | protein_coding | 1/18 | chr1 | 11980621 | ||||||
chr1:11980657
|
G | C | 1 | a0001c0001t0006g0037 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.-150+173G>C | MFN2 | ENSG00000116688.18 | transcript | ENST00000235329.10 | protein_coding | 1/18 | chr1 | 11980657 | ||||||
chr1:11980698
|
C | T | 1 | a0001c0001t0003g0303 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.-150+214C>T | MFN2 | ENSG00000116688.18 | transcript | ENST00000235329.10 | protein_coding | 1/18 | chr1 | 11980698 | ||||||
chr1:11980715
|
C | T | 10 | a0001c0001t0001g0299a0001c0001t0004g0296a0001c0001t0004g0297others(7): Show | 11 | HG01070.hp1 HG02109.hp2 HG02145.hp1 others(8): Show |
intron_variant | MODIFIER | c.-150+231C>T | MFN2 | ENSG00000116688.18 | transcript | ENST00000235329.10 | protein_coding | 1/18 | chr1 | 11980715 | ||||||
chr1:11980719
|
G | A | 1 | a0001c0017t0001g0049 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.-150+235G>A | MFN2 | ENSG00000116688.18 | transcript | ENST00000235329.10 | protein_coding | 1/18 | chr1 | 11980719 | ||||||
chr1:11980720
|
C | G | 1 | a0001c0017t0001g0049 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.-150+236C>G | MFN2 | ENSG00000116688.18 | transcript | ENST00000235329.10 | protein_coding | 1/18 | chr1 | 11980720 | ||||||
chr1:11980725
|
C | T | 1 | a0001c0017t0001g0049 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.-150+241C>T | MFN2 | ENSG00000116688.18 | transcript | ENST00000235329.10 | protein_coding | 1/18 | chr1 | 11980725 | ||||||
chr1:11980739
|
C | A | 1 | a0001c0001t0006g0038 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.-150+255C>A | MFN2 | ENSG00000116688.18 | transcript | ENST00000235329.10 | protein_coding | 1/18 | chr1 | 11980739 | ||||||
chr1:11980747
|
A | C | 2 | a0001c0003t0017g0292a0001c0003t0017g0293 | 2 | HG01109.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.-150+263A>C | MFN2 | ENSG00000116688.18 | transcript | ENST00000235329.10 | protein_coding | 1/18 | chr1 | 11980747 | ||||||
chr1:11980764
|
A | G | 2 | a0001c0001t0001g0290a0001c0001t0003g0291 | 2 | HG03491.hp1 HG04184.hp1 |
intron_variant | MODIFIER | c.-150+280A>G | MFN2 | ENSG00000116688.18 | transcript | ENST00000235329.10 | protein_coding | 1/18 | chr1 | 11980764 | ||||||
chr1:11980812
|
G | A | 2 | a0001c0005t0004g0294a0001c0005t0004g0295 | 2 | HG02895.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.-150+328G>A | MFN2 | ENSG00000116688.18 | transcript | ENST00000235329.10 | protein_coding | 1/18 | chr1 | 11980812 | ||||||
chr1:11980974
|
G | C | 2 | a0001c0003t0017g0292a0001c0003t0017g0293 | 2 | HG01109.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.-150+490G>C | MFN2 | ENSG00000116688.18 | transcript | ENST00000235329.10 | protein_coding | 1/18 | chr1 | 11980974 | ||||||
chr1:11981100
|
C | A | 4 | a0001c0001t0015g0050a0001c0001t0015g0051a0001c0001t0015g0053others(1): Show | 4 | HG02559.hp1 HG02723.hp2 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.-150+616C>A | MFN2 | ENSG00000116688.18 | transcript | ENST00000235329.10 | protein_coding | 1/18 | chr1 | 11981100 | ||||||
chr1:11981171
|
G | T | 1 | a0001c0001t0002g0289 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.-150+687G>T | MFN2 | ENSG00000116688.18 | transcript | ENST00000235329.10 | protein_coding | 1/18 | chr1 | 11981171 | ||||||
chr1:11981202
|
A | C | 1 | a0001c0017t0001g0049 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.-150+718A>C | MFN2 | ENSG00000116688.18 | transcript | ENST00000235329.10 | protein_coding | 1/18 | chr1 | 11981202 | ||||||
chr1:11981203
|
T | G | 1 | a0001c0001t0014g0039 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.-150+719T>G | MFN2 | ENSG00000116688.18 | transcript | ENST00000235329.10 | protein_coding | 1/18 | chr1 | 11981203 | ||||||
chr1:11981242
|
C | T | 1 | a0001c0001t0001g0288 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.-149-728C>T | MFN2 | ENSG00000116688.18 | transcript | ENST00000235329.10 | protein_coding | 1/18 | chr1 | 11981242 | ||||||
chr1:11981367
|
C | T | 1 | a0001c0001t0001g0287 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.-149-603C>T | MFN2 | ENSG00000116688.18 | transcript | ENST00000235329.10 | protein_coding | 1/18 | chr1 | 11981367 | ||||||
chr1:11981505
|
C | T | 2 | a0001c0003t0017g0292a0001c0003t0017g0293 | 2 | HG01109.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.-149-465C>T | MFN2 | ENSG00000116688.18 | transcript | ENST00000235329.10 | protein_coding | 1/18 | chr1 | 11981505 | ||||||
chr1:11981696
|
A | G | 1 | a0001c0001t0001g0286 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.-149-274A>G | MFN2 | ENSG00000116688.18 | transcript | ENST00000235329.10 | protein_coding | 1/18 | chr1 | 11981696 | ||||||
chr1:11981709
|
A | G | 1 | a0001c0001t0004g0047 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.-149-261A>G | MFN2 | ENSG00000116688.18 | transcript | ENST00000235329.10 | protein_coding | 1/18 | chr1 | 11981709 | ||||||
chr1:11981720
|
A | G | 1 | a0001c0001t0003g0285 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.-149-250A>G | MFN2 | ENSG00000116688.18 | transcript | ENST00000235329.10 | protein_coding | 1/18 | chr1 | 11981720 | ||||||
chr1:11981783
|
C | T | 1 | a0001c0001t0004g0284 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.-149-187C>T | MFN2 | ENSG00000116688.18 | transcript | ENST00000235329.10 | protein_coding | 1/18 | chr1 | 11981783 | ||||||
chr1:11981801
|
T | C | 1 | a0001c0001t0001g0054 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.-149-169T>C | MFN2 | ENSG00000116688.18 | transcript | ENST00000235329.10 | protein_coding | 1/18 | chr1 | 11981801 | ||||||
chr1:11981816
|
T | G | 1 | a0001c0017t0001g0049 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.-149-154T>G | MFN2 | ENSG00000116688.18 | transcript | ENST00000235329.10 | protein_coding | 1/18 | chr1 | 11981816 | ||||||
chr1:11981832
|
C | T | 5 | a0001c0003t0007g0035a0001c0003t0007g0280a0001c0003t0007g0281others(2): Show | 6 | HG01167.hp1 HG02145.hp2 HG02622.hp2 others(3): Show |
intron_variant | MODIFIER | c.-149-138C>T | MFN2 | ENSG00000116688.18 | transcript | ENST00000235329.10 | protein_coding | 1/18 | chr1 | 11981832 | ||||||
chr1:11981920
|
G | GTTTTGTT others(3): Show |
1 | a0001c0002t0005g0055 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.-149-46_-149-45ins others(10): Show |
MFN2 | ENSG00000116688.18 | transcript | ENST00000235329.10 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr1 | 11981920 | |||||
chr1:11981920
|
G | GTTTTTT | 11 | a0001c0001t0001g0113a0001c0001t0001g0114a0001c0001t0001g0115others(8): Show | 11 | HG01243.hp1 HG01884.hp1 HG02257.hp1 others(8): Show |
intron_variant | MODIFIER | c.-149-43_-149-38dup others(6): Show |
MFN2 | ENSG00000116688.18 | transcript | ENST00000235329.10 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr1 | 11981920 | |||||
chr1:11981920
|
G | GTTTTTTT | 95 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0009others(92): Show | 116 | HG00140.hp1 HG00558.hp1 HG00558.hp2 others(113): Show |
intron_variant | MODIFIER | c.-149-44_-149-38dup others(7): Show |
MFN2 | ENSG00000116688.18 | transcript | ENST00000235329.10 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr1 | 11981920 | |||||
chr1:11981920
|
G | GTTTTTTT others(1): Show |
103 | a0001c0001t0001g0203a0001c0001t0001g0205a0001c0001t0001g0206others(100): Show | 117 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(114): Show |
intron_variant | MODIFIER | c.-149-45_-149-38dup others(8): Show |
MFN2 | ENSG00000116688.18 | transcript | ENST00000235329.10 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr1 | 11981920 | |||||
chr1:11981920
|
G | GTTTTTTT others(2): Show |
21 | a0001c0001t0002g0273a0001c0001t0003g0274a0001c0001t0003g0275others(18): Show | 21 | HG01109.hp1 HG02027.hp1 HG02055.hp1 others(18): Show |
intron_variant | MODIFIER | c.-149-46_-149-38dup others(9): Show |
MFN2 | ENSG00000116688.18 | transcript | ENST00000235329.10 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr1 | 11981920 | |||||
chr1:11981920
|
G | GTTTTTTT others(3): Show |
1 | a0001c0001t0006g0046 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.-149-47_-149-38dup others(10): Show |
MFN2 | ENSG00000116688.18 | transcript | ENST00000235329.10 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr1 | 11981920 | |||||
chr1:11981940
|
G | T | 9 | a0001c0002t0005g0055a0001c0004t0004g0034a0001c0004t0004g0265others(6): Show | 10 | HG02083.hp2 HG04228.hp2 NA18906.hp2 others(7): Show |
intron_variant | MODIFIER | c.-149-30G>T | MFN2 | ENSG00000116688.18 | transcript | ENST00000235329.10 | protein_coding | 1/18 | chr1 | 11981940 | ||||||
chr1:11981955
|
T | G | 11 | a0001c0001t0004g0047a0001c0001t0006g0037a0001c0001t0006g0038others(8): Show | 11 | HG01192.hp2 HG01891.hp2 HG02280.hp1 others(8): Show |
intron_variant | MODIFIER | c.-149-15T>G | MFN2 | ENSG00000116688.18 | transcript | ENST00000235329.10 | protein_coding | 1/18 | chr1 | 11981955 | ||||||
chr1:11982204
|
A | G | 228 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0009others(225): Show | 262 | HG00140.hp1 HG00280.hp2 HG00408.hp1 others(259): Show |
intron_variant | MODIFIER | c.-5+90A>G | MFN2 | ENSG00000116688.18 | transcript | ENST00000235329.10 | protein_coding | 2/18 | chr1 | 11982204 | ||||||
chr1:11982241
|
C | T | 21 | a0001c0001t0013g0032a0001c0001t0013g0251a0001c0002t0005g0033others(18): Show | 23 | HG00408.hp1 HG00733.hp2 HG01192.hp1 others(20): Show |
intron_variant | MODIFIER | c.-5+127C>T | MFN2 | ENSG00000116688.18 | transcript | ENST00000235329.10 | protein_coding | 2/18 | chr1 | 11982241 | ||||||
chr1:11982386
|
C | T | 197 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0009others(194): Show | 226 | HG00140.hp1 HG00280.hp2 HG00408.hp1 others(223): Show |
intron_variant | MODIFIER | c.-5+272C>T | MFN2 | ENSG00000116688.18 | transcript | ENST00000235329.10 | protein_coding | 2/18 | chr1 | 11982386 | ||||||
chr1:11982449
|
T | C | 211 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0009others(208): Show | 242 | HG00140.hp1 HG00280.hp2 HG00408.hp1 others(239): Show |
intron_variant | MODIFIER | c.-5+335T>C | MFN2 | ENSG00000116688.18 | transcript | ENST00000235329.10 | protein_coding | 2/18 | chr1 | 11982449 | ||||||
chr1:11982497
|
A | G | 1 | a0003c0010t0002g0300 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.-5+383A>G | MFN2 | ENSG00000116688.18 | transcript | ENST00000235329.10 | protein_coding | 2/18 | chr1 | 11982497 | ||||||
chr1:11982682
|
C | T | 3 | a0001c0001t0004g0296a0001c0001t0004g0297a0001c0001t0004g0298 | 3 | HG02630.hp2 HG03516.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.-5+568C>T | MFN2 | ENSG00000116688.18 | transcript | ENST00000235329.10 | protein_coding | 2/18 | chr1 | 11982682 | ||||||
chr1:11982698
|
G | A | 162 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0009others(159): Show | 189 | HG00140.hp1 HG00280.hp2 HG00408.hp2 others(186): Show |
intron_variant | MODIFIER | c.-5+584G>A | MFN2 | ENSG00000116688.18 | transcript | ENST00000235329.10 | protein_coding | 2/18 | chr1 | 11982698 | ||||||
chr1:11982880
|
G | A | 1 | a0001c0001t0002g0056 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.-5+766G>A | MFN2 | ENSG00000116688.18 | transcript | ENST00000235329.10 | protein_coding | 2/18 | chr1 | 11982880 | ||||||
chr1:11983120
|
G | A | 2 | a0001c0001t0003g0123a0001c0001t0003g0124 | 2 | HG03491.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.-5+1006G>A | MFN2 | ENSG00000116688.18 | transcript | ENST00000235329.10 | protein_coding | 2/18 | chr1 | 11983120 | ||||||
chr1:11983134
|
G | A | 5 | a0001c0001t0003g0198a0001c0001t0003g0199a0001c0001t0003g0200others(2): Show | 5 | HG01934.hp1 NA18963.hp1 NA18973.hp1 others(2): Show |
intron_variant | MODIFIER | c.-5+1020G>A | MFN2 | ENSG00000116688.18 | transcript | ENST00000235329.10 | protein_coding | 2/18 | chr1 | 11983134 | ||||||
chr1:11983197
|
C | T | 10 | a0001c0001t0004g0016a0001c0001t0004g0195a0001c0001t0004g0196others(7): Show | 12 | HG02280.hp2 HG02572.hp2 HG02622.hp1 others(9): Show |
intron_variant | MODIFIER | c.-5+1083C>T | MFN2 | ENSG00000116688.18 | transcript | ENST00000235329.10 | protein_coding | 2/18 | chr1 | 11983197 | ||||||
chr1:11983217
|
G | A | 4 | a0001c0001t0002g0057a0001c0001t0002g0058a0001c0001t0002g0059others(1): Show | 4 | NA18940.hp1 NA18945.hp1 NA18951.hp2 others(1): Show |
intron_variant | MODIFIER | c.-5+1103G>A | MFN2 | ENSG00000116688.18 | transcript | ENST00000235329.10 | protein_coding | 2/18 | chr1 | 11983217 | ||||||
chr1:11983324
|
G | A | 1 | a0001c0001t0001g0113 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.-5+1210G>A | MFN2 | ENSG00000116688.18 | transcript | ENST00000235329.10 | protein_coding | 2/18 | chr1 | 11983324 | ||||||
chr1:11983412
|
T | C | 21 | a0001c0001t0013g0032a0001c0001t0013g0251a0001c0002t0005g0033others(18): Show | 23 | HG00408.hp1 HG00733.hp2 HG01192.hp1 others(20): Show |
intron_variant | MODIFIER | c.-5+1298T>C | MFN2 | ENSG00000116688.18 | transcript | ENST00000235329.10 | protein_coding | 2/18 | chr1 | 11983412 | ||||||
chr1:11983525
|
T | C | 1 | a0001c0001t0003g0202 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.-5+1411T>C | MFN2 | ENSG00000116688.18 | transcript | ENST00000235329.10 | protein_coding | 2/18 | chr1 | 11983525 | ||||||
chr1:11983600
|
T | A | 1 | a0001c0001t0002g0061 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.-5+1486T>A | MFN2 | ENSG00000116688.18 | transcript | ENST00000235329.10 | protein_coding | 2/18 | chr1 | 11983600 | ||||||
chr1:11983660
|
G | A | 198 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0009others(195): Show | 227 | HG00140.hp1 HG00280.hp2 HG00408.hp1 others(224): Show |
intron_variant | MODIFIER | c.-5+1546G>A | MFN2 | ENSG00000116688.18 | transcript | ENST00000235329.10 | protein_coding | 2/18 | chr1 | 11983660 | ||||||
chr1:11983807
|
G | A | 2 | a0001c0001t0001g0062a0001c0006t0001g0063 | 2 | HG02486.hp2 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.-5+1693G>A | MFN2 | ENSG00000116688.18 | transcript | ENST00000235329.10 | protein_coding | 2/18 | chr1 | 11983807 | ||||||
chr1:11983820
|
G | A | 7 | a0001c0001t0002g0006a0001c0001t0002g0017a0001c0001t0002g0064others(4): Show | 11 | HG01099.hp2 HG01123.hp2 HG01346.hp1 others(8): Show |
intron_variant | MODIFIER | c.-5+1706G>A | MFN2 | ENSG00000116688.18 | transcript | ENST00000235329.10 | protein_coding | 2/18 | chr1 | 11983820 | ||||||
chr1:11983869
|
G | A | 1 | a0001c0001t0004g0195 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.-5+1755G>A | MFN2 | ENSG00000116688.18 | transcript | ENST00000235329.10 | protein_coding | 2/18 | chr1 | 11983869 | ||||||
chr1:11984107
|
C | T | 211 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0009others(208): Show | 242 | HG00140.hp1 HG00280.hp2 HG00408.hp1 others(239): Show |
intron_variant | MODIFIER | c.-5+1993C>T | MFN2 | ENSG00000116688.18 | transcript | ENST00000235329.10 | protein_coding | 2/18 | chr1 | 11984107 | ||||||
chr1:11984294
|
G | A | 3 | a0001c0001t0012g0036a0001c0001t0012g0302a0003c0010t0002g0300 | 4 | HG02109.hp2 HG02145.hp1 HG02976.hp1 others(1): Show |
intron_variant | MODIFIER | c.-5+2180G>A | MFN2 | ENSG00000116688.18 | transcript | ENST00000235329.10 | protein_coding | 2/18 | chr1 | 11984294 | ||||||
chr1:11984323
|
T | C | 1 | a0001c0001t0002g0069 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.-5+2209T>C | MFN2 | ENSG00000116688.18 | transcript | ENST00000235329.10 | protein_coding | 2/18 | chr1 | 11984323 | ||||||
chr1:11984366
|
GGAGA | G | 8 | a0001c0004t0004g0034a0001c0004t0004g0265a0001c0004t0004g0267others(5): Show | 9 | HG02083.hp2 HG04228.hp2 NA18952.hp2 others(6): Show |
intron_variant | MODIFIER | c.-5+2256_-5+2259del others(4): Show |
MFN2 | ENSG00000116688.18 | transcript | ENST00000235329.10 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr1 | 11984366 | |||||
chr1:11984506
|
G | T | 8 | a0001c0004t0004g0034a0001c0004t0004g0265a0001c0004t0004g0267others(5): Show | 9 | HG02083.hp2 HG04228.hp2 NA18952.hp2 others(6): Show |
intron_variant | MODIFIER | c.-5+2392G>T | MFN2 | ENSG00000116688.18 | transcript | ENST00000235329.10 | protein_coding | 2/18 | chr1 | 11984506 | ||||||
chr1:11984615
|
C | A | 5 | a0001c0003t0007g0035a0001c0003t0007g0280a0001c0003t0007g0281others(2): Show | 6 | HG01167.hp1 HG02145.hp2 HG02622.hp2 others(3): Show |
intron_variant | MODIFIER | c.-5+2501C>A | MFN2 | ENSG00000116688.18 | transcript | ENST00000235329.10 | protein_coding | 2/18 | chr1 | 11984615 | ||||||
chr1:11984858
|
C | T | 1 | a0001c0001t0004g0195 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.-5+2744C>T | MFN2 | ENSG00000116688.18 | transcript | ENST00000235329.10 | protein_coding | 2/18 | chr1 | 11984858 | ||||||
chr1:11984868
|
G | A | 1 | a0001c0001t0004g0195 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.-5+2754G>A | MFN2 | ENSG00000116688.18 | transcript | ENST00000235329.10 | protein_coding | 2/18 | chr1 | 11984868 | ||||||
chr1:11984953
|
C | T | 2 | a0001c0003t0017g0292a0001c0003t0017g0293 | 2 | HG01109.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.-5+2839C>T | MFN2 | ENSG00000116688.18 | transcript | ENST00000235329.10 | protein_coding | 2/18 | chr1 | 11984953 | ||||||
chr1:11985074
|
G | A | 8 | a0001c0004t0004g0034a0001c0004t0004g0265a0001c0004t0004g0267others(5): Show | 9 | HG02083.hp2 HG04228.hp2 NA18952.hp2 others(6): Show |
intron_variant | MODIFIER | c.-5+2960G>A | MFN2 | ENSG00000116688.18 | transcript | ENST00000235329.10 | protein_coding | 2/18 | chr1 | 11985074 | ||||||
chr1:11985096
|
C | T | 1 | a0001c0001t0002g0056 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.-5+2982C>T | MFN2 | ENSG00000116688.18 | transcript | ENST00000235329.10 | protein_coding | 2/18 | chr1 | 11985096 | ||||||
chr1:11985455
|
C | CT | 15 | a0001c0001t0002g0027a0001c0001t0002g0060a0001c0001t0002g0068others(12): Show | 16 | HG00423.hp2 HG01109.hp1 HG01175.hp1 others(13): Show |
intron_variant | MODIFIER | c.-5+3368dupT | MFN2 | ENSG00000116688.18 | transcript | ENST00000235329.10 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr1 | 11985455 | |||||
chr1:11985455
|
C | CTT | 9 | a0001c0001t0004g0016a0001c0001t0004g0194a0001c0001t0004g0195others(6): Show | 12 | HG01167.hp1 HG02280.hp2 HG02451.hp2 others(9): Show |
intron_variant | MODIFIER | c.-5+3367_-5+3368dup others(2): Show |
MFN2 | ENSG00000116688.18 | transcript | ENST00000235329.10 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr1 | 11985455 | |||||
chr1:11985455
|
CT | C | 21 | a0001c0001t0001g0071a0001c0001t0001g0072a0001c0001t0001g0076others(18): Show | 24 | HG00140.hp1 HG00323.hp2 HG00639.hp1 others(21): Show |
intron_variant | MODIFIER | c.-5+3368delT | MFN2 | ENSG00000116688.18 | transcript | ENST00000235329.10 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr1 | 11985455 | |||||
chr1:11985455
|
CTTTTT | C | 11 | a0001c0001t0004g0047a0001c0001t0006g0037a0001c0001t0006g0038others(8): Show | 11 | HG01192.hp2 HG01891.hp2 HG02280.hp1 others(8): Show |
intron_variant | MODIFIER | c.-5+3364_-5+3368del others(5): Show |
MFN2 | ENSG00000116688.18 | transcript | ENST00000235329.10 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr1 | 11985455 | |||||
chr1:11985455
|
CTTTTTTT | C | 7 | a0001c0004t0004g0034a0001c0004t0004g0265a0001c0004t0004g0267others(4): Show | 8 | HG04228.hp2 NA18952.hp2 NA18967.hp2 others(5): Show |
intron_variant | MODIFIER | c.-5+3362_-5+3368del others(7): Show |
MFN2 | ENSG00000116688.18 | transcript | ENST00000235329.10 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr1 | 11985455 | |||||
chr1:11985455
|
CTTTTTTT others(3): Show |
C | 1 | a0001c0001t0002g0070 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.-5+3359_-5+3368del others(10): Show |
MFN2 | ENSG00000116688.18 | transcript | ENST00000235329.10 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr1 | 11985455 | |||||
chr1:11985482
|
T | A | 108 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0009others(105): Show | 132 | HG00140.hp1 HG00323.hp2 HG00558.hp1 others(129): Show |
intron_variant | MODIFIER | c.-5+3368T>A | MFN2 | ENSG00000116688.18 | transcript | ENST00000235329.10 | protein_coding | 2/18 | chr1 | 11985482 | ||||||
chr1:11985482
|
T | TA | 69 | a0001c0001t0001g0054a0001c0001t0001g0114a0001c0001t0001g0115others(66): Show | 75 | HG00280.hp2 HG00408.hp2 HG00423.hp1 others(72): Show |
intron_variant | MODIFIER | c.-5+3371dupA | MFN2 | ENSG00000116688.18 | transcript | ENST00000235329.10 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr1 | 11985482 | |||||
chr1:11985482
|
T | TTA | 27 | a0001c0001t0003g0189a0001c0001t0003g0246a0001c0001t0003g0247others(24): Show | 28 | HG00408.hp1 HG00438.hp1 HG00597.hp2 others(25): Show |
intron_variant | MODIFIER | c.-5+3368_-5+3369ins others(2): Show |
MFN2 | ENSG00000116688.18 | transcript | ENST00000235329.10 | protein_coding | 2/18 | chr1 | 11985482 | ||||||
chr1:11985495
|
TTCGC | T | 3 | a0001c0001t0003g0188a0001c0001t0003g0245a0001c0001t0003g0250 | 3 | NA18981.hp2 NA19085.hp2 NA19088.hp2 |
intron_variant | MODIFIER | c.-5+3384_-5+3387del others(4): Show |
MFN2 | ENSG00000116688.18 | transcript | ENST00000235329.10 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr1 | 11985495 | |||||
chr1:11985498
|
G | T | 211 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0009others(208): Show | 244 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(241): Show |
intron_variant | MODIFIER | c.-5+3384G>T | MFN2 | ENSG00000116688.18 | transcript | ENST00000235329.10 | protein_coding | 2/18 | chr1 | 11985498 | ||||||
chr1:11985540
|
C | T | 1 | a0001c0001t0001g0178 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.-5+3426C>T | MFN2 | ENSG00000116688.18 | transcript | ENST00000235329.10 | protein_coding | 2/18 | chr1 | 11985540 | ||||||
chr1:11985615
|
C | T | 8 | a0001c0004t0004g0034a0001c0004t0004g0265a0001c0004t0004g0267others(5): Show | 9 | HG02083.hp2 HG04228.hp2 NA18952.hp2 others(6): Show |
intron_variant | MODIFIER | c.-5+3501C>T | MFN2 | ENSG00000116688.18 | transcript | ENST00000235329.10 | protein_coding | 2/18 | chr1 | 11985615 | ||||||
chr1:11985656
|
C | T | 1 | a0001c0001t0019g0107 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.-4-3509C>T | MFN2 | ENSG00000116688.18 | transcript | ENST00000235329.10 | protein_coding | 2/18 | chr1 | 11985656 | ||||||
chr1:11985725
|
C | T | 21 | a0001c0001t0013g0032a0001c0001t0013g0251a0001c0002t0005g0033others(18): Show | 23 | HG00408.hp1 HG00733.hp2 HG01192.hp1 others(20): Show |
intron_variant | MODIFIER | c.-4-3440C>T | MFN2 | ENSG00000116688.18 | transcript | ENST00000235329.10 | protein_coding | 2/18 | chr1 | 11985725 | ||||||
chr1:11985757
|
C | T | 2 | a0001c0001t0013g0032a0001c0001t0013g0251 | 3 | HG02970.hp2 HG03209.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.-4-3408C>T | MFN2 | ENSG00000116688.18 | transcript | ENST00000235329.10 | protein_coding | 2/18 | chr1 | 11985757 | ||||||
chr1:11985783
|
A | G | 5 | a0001c0003t0007g0035a0001c0003t0007g0280a0001c0003t0007g0281others(2): Show | 6 | HG01167.hp1 HG02145.hp2 HG02622.hp2 others(3): Show |
intron_variant | MODIFIER | c.-4-3382A>G | MFN2 | ENSG00000116688.18 | transcript | ENST00000235329.10 | protein_coding | 2/18 | chr1 | 11985783 | ||||||
chr1:11985833
|
G | A | 1 | a0001c0001t0001g0054 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.-4-3332G>A | MFN2 | ENSG00000116688.18 | transcript | ENST00000235329.10 | protein_coding | 2/18 | chr1 | 11985833 | ||||||
chr1:11985850
|
A | G | 1 | a0001c0005t0004g0122 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.-4-3315A>G | MFN2 | ENSG00000116688.18 | transcript | ENST00000235329.10 | protein_coding | 2/18 | chr1 | 11985850 | ||||||
chr1:11985861
|
A | G | 2 | a0001c0001t0001g0072a0001c0001t0001g0074 | 2 | HG00639.hp1 HG04204.hp2 |
intron_variant | MODIFIER | c.-4-3304A>G | MFN2 | ENSG00000116688.18 | transcript | ENST00000235329.10 | protein_coding | 2/18 | chr1 | 11985861 | ||||||
chr1:11985866
|
C | G | 319 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(316): Show | 393 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(390): Show |
intron_variant | MODIFIER | c.-4-3299C>G | MFN2 | ENSG00000116688.18 | transcript | ENST00000235329.10 | protein_coding | 2/18 | chr1 | 11985866 | ||||||
chr1:11985878
|
C | T | 1 | a0001c0001t0001g0177 | 1 | NA19056.hp2 | intron_variant | MODIFIER | c.-4-3287C>T | MFN2 | ENSG00000116688.18 | transcript | ENST00000235329.10 | protein_coding | 2/18 | chr1 | 11985878 | ||||||
chr1:11985902
|
T | A | 1 | a0001c0001t0010g0020 | 2 | HG02257.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.-4-3263T>A | MFN2 | ENSG00000116688.18 | transcript | ENST00000235329.10 | protein_coding | 2/18 | chr1 | 11985902 | ||||||
chr1:11986006
|
G | T | 214 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0009others(211): Show | 247 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(244): Show |
intron_variant | MODIFIER | c.-4-3159G>T | MFN2 | ENSG00000116688.18 | transcript | ENST00000235329.10 | protein_coding | 2/18 | chr1 | 11986006 | ||||||
chr1:11986032
|
G | A | 84 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0009others(81): Show | 107 | HG00140.hp1 HG00323.hp2 HG00558.hp1 others(104): Show |
intron_variant | MODIFIER | c.-4-3133G>A | MFN2 | ENSG00000116688.18 | transcript | ENST00000235329.10 | protein_coding | 2/18 | chr1 | 11986032 | ||||||
chr1:11986277
|
C | G | 206 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0009others(203): Show | 238 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(235): Show |
intron_variant | MODIFIER | c.-4-2888C>G | MFN2 | ENSG00000116688.18 | transcript | ENST00000235329.10 | protein_coding | 2/18 | chr1 | 11986277 | ||||||
chr1:11986490
|
G | A | 10 | a0001c0001t0004g0016a0001c0001t0004g0195a0001c0001t0004g0196others(7): Show | 12 | HG02280.hp2 HG02572.hp2 HG02622.hp1 others(9): Show |
intron_variant | MODIFIER | c.-4-2675G>A | MFN2 | ENSG00000116688.18 | transcript | ENST00000235329.10 | protein_coding | 2/18 | chr1 | 11986490 | ||||||
chr1:11986591
|
C | CT | 21 | a0001c0001t0001g0173a0001c0001t0001g0215a0001c0001t0002g0273others(18): Show | 24 | HG01884.hp2 HG02055.hp1 HG02109.hp2 others(21): Show |
intron_variant | MODIFIER | c.-4-2557dupT | MFN2 | ENSG00000116688.18 | transcript | ENST00000235329.10 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr1 | 11986591 | |||||
chr1:11986591
|
CT | C | 8 | a0001c0001t0001g0130a0001c0001t0001g0131a0001c0001t0001g0163others(5): Show | 8 | HG00408.hp2 HG01978.hp1 HG02896.hp2 others(5): Show |
intron_variant | MODIFIER | c.-4-2557delT | MFN2 | ENSG00000116688.18 | transcript | ENST00000235329.10 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr1 | 11986591 | |||||
chr1:11986626
|
T | C | 2 | a0001c0001t0001g0054a0001c0001t0004g0284 | 2 | HG02615.hp1 HG02965.hp1 |
intron_variant | MODIFIER | c.-4-2539T>C | MFN2 | ENSG00000116688.18 | transcript | ENST00000235329.10 | protein_coding | 2/18 | chr1 | 11986626 | ||||||
chr1:11986701
|
G | A | 7 | a0001c0003t0007g0035a0001c0003t0007g0280a0001c0003t0007g0281others(4): Show | 8 | HG01109.hp1 HG01167.hp1 HG02145.hp2 others(5): Show |
intron_variant | MODIFIER | c.-4-2464G>A | MFN2 | ENSG00000116688.18 | transcript | ENST00000235329.10 | protein_coding | 2/18 | chr1 | 11986701 | ||||||
chr1:11986710
|
C | T | 10 | a0001c0001t0004g0016a0001c0001t0004g0195a0001c0001t0004g0196others(7): Show | 12 | HG02280.hp2 HG02572.hp2 HG02622.hp1 others(9): Show |
intron_variant | MODIFIER | c.-4-2455C>T | MFN2 | ENSG00000116688.18 | transcript | ENST00000235329.10 | protein_coding | 2/18 | chr1 | 11986710 | ||||||
chr1:11986772
|
G | A | 21 | a0001c0001t0013g0032a0001c0001t0013g0251a0001c0002t0005g0033others(18): Show | 23 | HG00408.hp1 HG00733.hp2 HG01192.hp1 others(20): Show |
intron_variant | MODIFIER | c.-4-2393G>A | MFN2 | ENSG00000116688.18 | transcript | ENST00000235329.10 | protein_coding | 2/18 | chr1 | 11986772 | ||||||
chr1:11986823
|
C | T | 97 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0009others(94): Show | 121 | HG00140.hp1 HG00323.hp2 HG00558.hp1 others(118): Show |
intron_variant | MODIFIER | c.-4-2342C>T | MFN2 | ENSG00000116688.18 | transcript | ENST00000235329.10 | protein_coding | 2/18 | chr1 | 11986823 | ||||||
chr1:11986971
|
T | C | 214 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0009others(211): Show | 247 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(244): Show |
intron_variant | MODIFIER | c.-4-2194T>C | MFN2 | ENSG00000116688.18 | transcript | ENST00000235329.10 | protein_coding | 2/18 | chr1 | 11986971 | ||||||
chr1:11987139
|
G | GTC | 222 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0009others(219): Show | 256 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(253): Show |
intron_variant | MODIFIER | c.-4-2024_-4-2023dup others(2): Show |
MFN2 | ENSG00000116688.18 | transcript | ENST00000235329.10 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr1 | 11987139 | |||||
chr1:11987176
|
T | C | 222 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0009others(219): Show | 256 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(253): Show |
intron_variant | MODIFIER | c.-4-1989T>C | MFN2 | ENSG00000116688.18 | transcript | ENST00000235329.10 | protein_coding | 2/18 | chr1 | 11987176 | ||||||
chr1:11987247
|
G | A | 5 | a0001c0003t0007g0035a0001c0003t0007g0280a0001c0003t0007g0281others(2): Show | 6 | HG01167.hp1 HG02145.hp2 HG02622.hp2 others(3): Show |
intron_variant | MODIFIER | c.-4-1918G>A | MFN2 | ENSG00000116688.18 | transcript | ENST00000235329.10 | protein_coding | 2/18 | chr1 | 11987247 | ||||||
chr1:11987302
|
ACT | A | 21 | a0001c0001t0013g0032a0001c0001t0013g0251a0001c0002t0005g0033others(18): Show | 23 | HG00408.hp1 HG00733.hp2 HG01192.hp1 others(20): Show |
intron_variant | MODIFIER | c.-4-1860_-4-1859del others(2): Show |
MFN2 | ENSG00000116688.18 | transcript | ENST00000235329.10 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr1 | 11987302 | |||||
chr1:11987311
|
C | CA | 11 | a0001c0001t0002g0078a0001c0001t0002g0079a0001c0001t0002g0108others(8): Show | 12 | HG02080.hp2 HG02083.hp2 HG04228.hp2 others(9): Show |
intron_variant | MODIFIER | c.-4-1838dupA | MFN2 | ENSG00000116688.18 | transcript | ENST00000235329.10 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr1 | 11987311 | |||||
chr1:11987311
|
CA | C | 210 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0009others(207): Show | 243 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(240): Show |
intron_variant | MODIFIER | c.-4-1838delA | MFN2 | ENSG00000116688.18 | transcript | ENST00000235329.10 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr1 | 11987311 | |||||
chr1:11987370
|
C | T | 21 | a0001c0001t0013g0032a0001c0001t0013g0251a0001c0002t0005g0033others(18): Show | 23 | HG00408.hp1 HG00733.hp2 HG01192.hp1 others(20): Show |
intron_variant | MODIFIER | c.-4-1795C>T | MFN2 | ENSG00000116688.18 | transcript | ENST00000235329.10 | protein_coding | 2/18 | chr1 | 11987370 | ||||||
chr1:11987560
|
G | C | 8 | a0001c0004t0004g0034a0001c0004t0004g0265a0001c0004t0004g0267others(5): Show | 9 | HG02083.hp2 HG04228.hp2 NA18952.hp2 others(6): Show |
intron_variant | MODIFIER | c.-4-1605G>C | MFN2 | ENSG00000116688.18 | transcript | ENST00000235329.10 | protein_coding | 2/18 | chr1 | 11987560 | ||||||
chr1:11987572
|
G | A | 2 | a0001c0001t0013g0032a0001c0001t0013g0251 | 3 | HG02970.hp2 HG03209.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.-4-1593G>A | MFN2 | ENSG00000116688.18 | transcript | ENST00000235329.10 | protein_coding | 2/18 | chr1 | 11987572 | ||||||
chr1:11987587
|
G | A | 10 | a0001c0001t0004g0016a0001c0001t0004g0195a0001c0001t0004g0196others(7): Show | 12 | HG02280.hp2 HG02572.hp2 HG02622.hp1 others(9): Show |
intron_variant | MODIFIER | c.-4-1578G>A | MFN2 | ENSG00000116688.18 | transcript | ENST00000235329.10 | protein_coding | 2/18 | chr1 | 11987587 | ||||||
chr1:11987629
|
C | CA | 5 | a0001c0001t0001g0128a0001c0001t0001g0162a0001c0001t0003g0211others(2): Show | 5 | HG01169.hp2 HG01975.hp1 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.-4-1535dupA | MFN2 | ENSG00000116688.18 | transcript | ENST00000235329.10 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr1 | 11987629 | |||||
chr1:11987629
|
C | CAA | 190 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0009others(187): Show | 223 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(220): Show |
intron_variant | MODIFIER | c.-4-1535_-4-1534ins others(2): Show |
MFN2 | ENSG00000116688.18 | transcript | ENST00000235329.10 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr1 | 11987629 | |||||
chr1:11987629
|
C | CAAA | 27 | a0001c0001t0001g0062a0001c0001t0001g0114a0001c0001t0001g0132others(24): Show | 28 | HG00738.hp2 HG01109.hp1 HG01934.hp1 others(25): Show |
intron_variant | MODIFIER | c.-4-1535_-4-1534ins others(3): Show |
MFN2 | ENSG00000116688.18 | transcript | ENST00000235329.10 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr1 | 11987629 | |||||
chr1:11987631
|
G | A | 222 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0009others(219): Show | 256 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(253): Show |
intron_variant | MODIFIER | c.-4-1534G>A | MFN2 | ENSG00000116688.18 | transcript | ENST00000235329.10 | protein_coding | 2/18 | chr1 | 11987631 | ||||||
chr1:11987672
|
G | A | 7 | a0001c0003t0007g0035a0001c0003t0007g0280a0001c0003t0007g0281others(4): Show | 8 | HG01109.hp1 HG01167.hp1 HG02145.hp2 others(5): Show |
intron_variant | MODIFIER | c.-4-1493G>A | MFN2 | ENSG00000116688.18 | transcript | ENST00000235329.10 | protein_coding | 2/18 | chr1 | 11987672 | ||||||
chr1:11987763
|
C | T | 7 | a0001c0003t0007g0035a0001c0003t0007g0280a0001c0003t0007g0281others(4): Show | 8 | HG01109.hp1 HG01167.hp1 HG02145.hp2 others(5): Show |
intron_variant | MODIFIER | c.-4-1402C>T | MFN2 | ENSG00000116688.18 | transcript | ENST00000235329.10 | protein_coding | 2/18 | chr1 | 11987763 | ||||||
chr1:11988022
|
C | T | 1 | a0001c0001t0002g0069 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.-4-1143C>T | MFN2 | ENSG00000116688.18 | transcript | ENST00000235329.10 | protein_coding | 2/18 | chr1 | 11988022 | ||||||
chr1:11988042
|
T | C | 1 | a0001c0001t0002g0080 | 1 | NA19083.hp2 | intron_variant | MODIFIER | c.-4-1123T>C | MFN2 | ENSG00000116688.18 | transcript | ENST00000235329.10 | protein_coding | 2/18 | chr1 | 11988042 | ||||||
chr1:11988044
|
T | C | 1 | a0001c0001t0002g0080 | 1 | NA19083.hp2 | intron_variant | MODIFIER | c.-4-1121T>C | MFN2 | ENSG00000116688.18 | transcript | ENST00000235329.10 | protein_coding | 2/18 | chr1 | 11988044 | ||||||
chr1:11988045
|
G | A | 1 | a0001c0001t0002g0080 | 1 | NA19083.hp2 | intron_variant | MODIFIER | c.-4-1120G>A | MFN2 | ENSG00000116688.18 | transcript | ENST00000235329.10 | protein_coding | 2/18 | chr1 | 11988045 | ||||||
chr1:11988048
|
G | C | 1 | a0001c0001t0002g0080 | 1 | NA19083.hp2 | intron_variant | MODIFIER | c.-4-1117G>C | MFN2 | ENSG00000116688.18 | transcript | ENST00000235329.10 | protein_coding | 2/18 | chr1 | 11988048 | ||||||
chr1:11988050
|
A | C | 1 | a0001c0001t0002g0080 | 1 | NA19083.hp2 | intron_variant | MODIFIER | c.-4-1115A>C | MFN2 | ENSG00000116688.18 | transcript | ENST00000235329.10 | protein_coding | 2/18 | chr1 | 11988050 | ||||||
chr1:11988054
|
C | A | 1 | a0001c0001t0002g0080 | 1 | NA19083.hp2 | intron_variant | MODIFIER | c.-4-1111C>A | MFN2 | ENSG00000116688.18 | transcript | ENST00000235329.10 | protein_coding | 2/18 | chr1 | 11988054 | ||||||
chr1:11988056
|
G | T | 1 | a0001c0001t0002g0080 | 1 | NA19083.hp2 | intron_variant | MODIFIER | c.-4-1109G>T | MFN2 | ENSG00000116688.18 | transcript | ENST00000235329.10 | protein_coding | 2/18 | chr1 | 11988056 | ||||||
chr1:11988058
|
G | T | 1 | a0001c0001t0002g0080 | 1 | NA19083.hp2 | intron_variant | MODIFIER | c.-4-1107G>T | MFN2 | ENSG00000116688.18 | transcript | ENST00000235329.10 | protein_coding | 2/18 | chr1 | 11988058 | ||||||
chr1:11988061
|
A | G | 1 | a0001c0001t0002g0080 | 1 | NA19083.hp2 | intron_variant | MODIFIER | c.-4-1104A>G | MFN2 | ENSG00000116688.18 | transcript | ENST00000235329.10 | protein_coding | 2/18 | chr1 | 11988061 | ||||||
chr1:11988073
|
A | G | 214 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0009others(211): Show | 247 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(244): Show |
intron_variant | MODIFIER | c.-4-1092A>G | MFN2 | ENSG00000116688.18 | transcript | ENST00000235329.10 | protein_coding | 2/18 | chr1 | 11988073 | ||||||
chr1:11988080
|
GTT | G | 52 | a0001c0001t0001g0225a0001c0001t0001g0237a0001c0001t0003g0003others(49): Show | 58 | HG00280.hp2 HG00408.hp2 HG00423.hp1 others(55): Show |
intron_variant | MODIFIER | c.-4-1081_-4-1080del others(2): Show |
MFN2 | ENSG00000116688.18 | transcript | ENST00000235329.10 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr1 | 11988080 | |||||
chr1:11988082
|
T | G | 1 | a0001c0004t0004g0265 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.-4-1083T>G | MFN2 | ENSG00000116688.18 | transcript | ENST00000235329.10 | protein_coding | 2/18 | chr1 | 11988082 | ||||||
chr1:11988082
|
T | TTGTG | 14 | a0001c0001t0001g0157a0001c0001t0001g0158a0001c0001t0001g0159others(11): Show | 15 | HG02083.hp2 HG02132.hp1 HG02523.hp1 others(12): Show |
intron_variant | MODIFIER | c.-4-1082_-4-1081ins others(4): Show |
MFN2 | ENSG00000116688.18 | transcript | ENST00000235329.10 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr1 | 11988082 | |||||
chr1:11988082
|
T | TTGTGTG | 115 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0009others(112): Show | 139 | HG00323.hp2 HG00408.hp1 HG00558.hp1 others(136): Show |
intron_variant | MODIFIER | c.-4-1082_-4-1081ins others(6): Show |
MFN2 | ENSG00000116688.18 | transcript | ENST00000235329.10 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr1 | 11988082 | |||||
chr1:11988082
|
T | TTGTGTGT others(1): Show |
28 | a0001c0001t0001g0013a0001c0001t0001g0029a0001c0001t0001g0054others(25): Show | 31 | HG01243.hp1 HG01884.hp1 HG01884.hp2 others(28): Show |
intron_variant | MODIFIER | c.-4-1082_-4-1081ins others(8): Show |
MFN2 | ENSG00000116688.18 | transcript | ENST00000235329.10 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr1 | 11988082 | |||||
chr1:11988082
|
T | TTGTGTGT others(3): Show |
6 | a0001c0001t0001g0073a0001c0001t0001g0125a0001c0001t0001g0135others(3): Show | 6 | HG00140.hp1 HG01123.hp1 HG02280.hp1 others(3): Show |
intron_variant | MODIFIER | c.-4-1082_-4-1081ins others(10): Show |
MFN2 | ENSG00000116688.18 | transcript | ENST00000235329.10 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr1 | 11988082 | |||||
chr1:11988082
|
T | TTGTGTGT others(5): Show |
3 | a0001c0001t0006g0037a0001c0001t0006g0040a0001c0001t0006g0046 | 3 | HG01192.hp2 HG02647.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.-4-1082_-4-1081ins others(12): Show |
MFN2 | ENSG00000116688.18 | transcript | ENST00000235329.10 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr1 | 11988082 | |||||
chr1:11988084
|
T | G | 170 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0009others(167): Show | 198 | HG00140.hp1 HG00323.hp2 HG00408.hp1 others(195): Show |
intron_variant | MODIFIER | c.-4-1081T>G | MFN2 | ENSG00000116688.18 | transcript | ENST00000235329.10 | protein_coding | 2/18 | chr1 | 11988084 | ||||||
chr1:11988084
|
T | TTG | 3 | a0001c0001t0004g0016a0001c0001t0004g0195a0001c0001t0004g0197 | 5 | HG02280.hp2 HG02572.hp2 HG02622.hp1 others(2): Show |
intron_variant | MODIFIER | c.-4-1057_-4-1056dup others(2): Show |
MFN2 | ENSG00000116688.18 | transcript | ENST00000235329.10 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr1 | 11988084 | |||||
chr1:11988086
|
G | T | 1 | a0001c0005t0004g0294 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.-4-1079G>T | MFN2 | ENSG00000116688.18 | transcript | ENST00000235329.10 | protein_coding | 2/18 | chr1 | 11988086 | ||||||
chr1:11988108
|
G | T | 3 | a0001c0001t0002g0079a0001c0001t0002g0104a0001c0001t0003g0221 | 3 | HG02080.hp2 HG02735.hp2 HG04199.hp1 |
intron_variant | MODIFIER | c.-4-1057G>T | MFN2 | ENSG00000116688.18 | transcript | ENST00000235329.10 | protein_coding | 2/18 | chr1 | 11988108 | ||||||
chr1:11988247
|
G | A | 3 | a0001c0001t0012g0036a0001c0001t0012g0302a0003c0010t0002g0300 | 4 | HG02109.hp2 HG02145.hp1 HG02976.hp1 others(1): Show |
intron_variant | MODIFIER | c.-4-918G>A | MFN2 | ENSG00000116688.18 | transcript | ENST00000235329.10 | protein_coding | 2/18 | chr1 | 11988247 | ||||||
chr1:11988267
|
A | G | 8 | a0001c0004t0004g0034a0001c0004t0004g0265a0001c0004t0004g0267others(5): Show | 9 | HG02083.hp2 HG04228.hp2 NA18952.hp2 others(6): Show |
intron_variant | MODIFIER | c.-4-898A>G | MFN2 | ENSG00000116688.18 | transcript | ENST00000235329.10 | protein_coding | 2/18 | chr1 | 11988267 | ||||||
chr1:11988403
|
G | GT | 169 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0009others(166): Show | 199 | HG00323.hp2 HG00408.hp1 HG00438.hp2 others(196): Show |
intron_variant | MODIFIER | c.-4-745dupT | MFN2 | ENSG00000116688.18 | transcript | ENST00000235329.10 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr1 | 11988403 | |||||
chr1:11988403
|
G | GTT | 61 | a0001c0001t0001g0125a0001c0001t0001g0131a0001c0001t0001g0178others(58): Show | 67 | HG00140.hp1 HG00280.hp2 HG00408.hp2 others(64): Show |
intron_variant | MODIFIER | c.-4-746_-4-745dupTT | MFN2 | ENSG00000116688.18 | transcript | ENST00000235329.10 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr1 | 11988403 | |||||
chr1:11988409
|
T | G | 8 | a0001c0004t0004g0034a0001c0004t0004g0265a0001c0004t0004g0267others(5): Show | 9 | HG02083.hp2 HG04228.hp2 NA18952.hp2 others(6): Show |
intron_variant | MODIFIER | c.-4-756T>G | MFN2 | ENSG00000116688.18 | transcript | ENST00000235329.10 | protein_coding | 2/18 | chr1 | 11988409 | ||||||
chr1:11988425
|
A | G | 1 | a0001c0001t0003g0202 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.-4-740A>G | MFN2 | ENSG00000116688.18 | transcript | ENST00000235329.10 | protein_coding | 2/18 | chr1 | 11988425 | ||||||
chr1:11988532
|
C | T | 6 | a0001c0001t0002g0273a0001c0001t0004g0030a0001c0001t0004g0191others(3): Show | 7 | HG02055.hp1 HG02451.hp2 HG02572.hp1 others(4): Show |
intron_variant | MODIFIER | c.-4-633C>T | MFN2 | ENSG00000116688.18 | transcript | ENST00000235329.10 | protein_coding | 2/18 | chr1 | 11988532 | ||||||
chr1:11988538
|
C | T | 173 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0009others(170): Show | 203 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(200): Show |
intron_variant | MODIFIER | c.-4-627C>T | MFN2 | ENSG00000116688.18 | transcript | ENST00000235329.10 | protein_coding | 2/18 | chr1 | 11988538 | ||||||
chr1:11988608
|
G | A | 8 | a0001c0004t0004g0034a0001c0004t0004g0265a0001c0004t0004g0267others(5): Show | 9 | HG02083.hp2 HG04228.hp2 NA18952.hp2 others(6): Show |
intron_variant | MODIFIER | c.-4-557G>A | MFN2 | ENSG00000116688.18 | transcript | ENST00000235329.10 | protein_coding | 2/18 | chr1 | 11988608 | ||||||
chr1:11988614
|
G | A | 2 | a0001c0001t0002g0081a0001c0001t0002g0109 | 2 | HG00140.hp2 HG01175.hp1 |
intron_variant | MODIFIER | c.-4-551G>A | MFN2 | ENSG00000116688.18 | transcript | ENST00000235329.10 | protein_coding | 2/18 | chr1 | 11988614 | ||||||
chr1:11988619
|
C | T | 1 | a0001c0001t0001g0134 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.-4-546C>T | MFN2 | ENSG00000116688.18 | transcript | ENST00000235329.10 | protein_coding | 2/18 | chr1 | 11988619 | ||||||
chr1:11988826
|
A | G | 222 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0009others(219): Show | 256 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(253): Show |
intron_variant | MODIFIER | c.-4-339A>G | MFN2 | ENSG00000116688.18 | transcript | ENST00000235329.10 | protein_coding | 2/18 | chr1 | 11988826 | ||||||
chr1:11988944
|
C | A | 2 | a0001c0001t0004g0016a0001c0001t0004g0197 | 4 | HG02280.hp2 HG02572.hp2 HG02622.hp1 others(1): Show |
intron_variant | MODIFIER | c.-4-221C>A | MFN2 | ENSG00000116688.18 | transcript | ENST00000235329.10 | protein_coding | 2/18 | chr1 | 11988944 | ||||||
chr1:11989014
|
C | G | 1 | a0001c0001t0001g0015 | 3 | HG02071.hp2 NA19080.hp2 NA19088.hp1 |
intron_variant | MODIFIER | c.-4-151C>G | MFN2 | ENSG00000116688.18 | transcript | ENST00000235329.10 | protein_coding | 2/18 | chr1 | 11989014 | ||||||
chr1:11989120
|
C | T | 1 | a0001c0001t0002g0025 | 2 | HG03490.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.-4-45C>T | MFN2 | ENSG00000116688.18 | transcript | ENST00000235329.10 | protein_coding | 2/18 | chr1 | 11989120 | ||||||
chr1:11989561
|
CAT | C | 7 | a0001c0003t0007g0035a0001c0003t0007g0280a0001c0003t0007g0281others(4): Show | 8 | HG01109.hp1 HG01167.hp1 HG02145.hp2 others(5): Show |
intron_variant | MODIFIER | c.175+219_175+220del others(2): Show |
MFN2 | ENSG00000116688.18 | transcript | ENST00000235329.10 | protein_coding | 3/18 | chr1 | 11989561 | ||||||
chr1:11989651
|
C | A | 3 | a0001c0001t0003g0220a0001c0001t0003g0223a0001c0001t0003g0224 | 3 | NA18970.hp2 NA19011.hp1 NA19056.hp1 |
intron_variant | MODIFIER | c.175+308C>A | MFN2 | ENSG00000116688.18 | transcript | ENST00000235329.10 | protein_coding | 3/18 | chr1 | 11989651 | ||||||
chr1:11989779
|
C | T | 1 | a0001c0001t0026g0272 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.175+436C>T | MFN2 | ENSG00000116688.18 | transcript | ENST00000235329.10 | protein_coding | 3/18 | chr1 | 11989779 | ||||||
chr1:11989814
|
A | T | 1 | a0001c0001t0002g0070 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.175+471A>T | MFN2 | ENSG00000116688.18 | transcript | ENST00000235329.10 | protein_coding | 3/18 | chr1 | 11989814 | ||||||
chr1:11989858
|
A | G | 2 | a0001c0002t0005g0263a0001c0002t0005g0264 | 2 | HG00733.hp2 HG01192.hp1 |
intron_variant | MODIFIER | c.175+515A>G | MFN2 | ENSG00000116688.18 | transcript | ENST00000235329.10 | protein_coding | 3/18 | chr1 | 11989858 | ||||||
chr1:11990004
|
T | C | 1 | a0001c0001t0001g0225 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.175+661T>C | MFN2 | ENSG00000116688.18 | transcript | ENST00000235329.10 | protein_coding | 3/18 | chr1 | 11990004 | ||||||
chr1:11990169
|
A | G | 2 | a0001c0001t0004g0047a0001c0001t0025g0301 | 2 | HG01891.hp2 HG02559.hp2 |
intron_variant | MODIFIER | c.175+826A>G | MFN2 | ENSG00000116688.18 | transcript | ENST00000235329.10 | protein_coding | 3/18 | chr1 | 11990169 | ||||||
chr1:11990577
|
T | C | 214 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0009others(211): Show | 247 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(244): Show |
intron_variant | MODIFIER | c.175+1234T>C | MFN2 | ENSG00000116688.18 | transcript | ENST00000235329.10 | protein_coding | 3/18 | chr1 | 11990577 | ||||||
chr1:11990872
|
C | T | 2 | a0001c0001t0013g0032a0001c0001t0013g0251 | 3 | HG02970.hp2 HG03209.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.175+1529C>T | MFN2 | ENSG00000116688.18 | transcript | ENST00000235329.10 | protein_coding | 3/18 | chr1 | 11990872 | ||||||
chr1:11990891
|
G | A | 1 | a0001c0001t0018g0106 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.175+1548G>A | MFN2 | ENSG00000116688.18 | transcript | ENST00000235329.10 | protein_coding | 3/18 | chr1 | 11990891 | ||||||
chr1:11990929
|
T | C | 15 | a0001c0003t0007g0035a0001c0003t0007g0280a0001c0003t0007g0281others(12): Show | 17 | HG01109.hp1 HG01167.hp1 HG02083.hp2 others(14): Show |
intron_variant | MODIFIER | c.175+1586T>C | MFN2 | ENSG00000116688.18 | transcript | ENST00000235329.10 | protein_coding | 3/18 | chr1 | 11990929 | ||||||
chr1:11991071
|
C | T | 1 | a0001c0001t0001g0213 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.176-1484C>T | MFN2 | ENSG00000116688.18 | transcript | ENST00000235329.10 | protein_coding | 3/18 | chr1 | 11991071 | ||||||
chr1:11991279
|
G | A | 7 | a0001c0003t0007g0035a0001c0003t0007g0280a0001c0003t0007g0281others(4): Show | 8 | HG01109.hp1 HG01167.hp1 HG02145.hp2 others(5): Show |
intron_variant | MODIFIER | c.176-1276G>A | MFN2 | ENSG00000116688.18 | transcript | ENST00000235329.10 | protein_coding | 3/18 | chr1 | 11991279 | ||||||
chr1:11991361
|
C | T | 7 | a0001c0001t0001g0173a0001c0001t0004g0048a0001c0001t0004g0129others(4): Show | 7 | HG01884.hp2 HG02886.hp2 HG02896.hp1 others(4): Show |
intron_variant | MODIFIER | c.176-1194C>T | MFN2 | ENSG00000116688.18 | transcript | ENST00000235329.10 | protein_coding | 3/18 | chr1 | 11991361 | ||||||
chr1:11991462
|
C | G | 8 | a0001c0004t0004g0034a0001c0004t0004g0265a0001c0004t0004g0267others(5): Show | 9 | HG02083.hp2 HG04228.hp2 NA18952.hp2 others(6): Show |
intron_variant | MODIFIER | c.176-1093C>G | MFN2 | ENSG00000116688.18 | transcript | ENST00000235329.10 | protein_coding | 3/18 | chr1 | 11991462 | ||||||
chr1:11991651
|
G | A | 54 | a0001c0001t0001g0225a0001c0001t0001g0237a0001c0001t0003g0003others(51): Show | 60 | HG00280.hp2 HG00408.hp2 HG00423.hp1 others(57): Show |
intron_variant | MODIFIER | c.176-904G>A | MFN2 | ENSG00000116688.18 | transcript | ENST00000235329.10 | protein_coding | 3/18 | chr1 | 11991651 | ||||||
chr1:11991690
|
C | T | 1 | a0001c0001t0001g0171 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.176-865C>T | MFN2 | ENSG00000116688.18 | transcript | ENST00000235329.10 | protein_coding | 3/18 | chr1 | 11991690 | ||||||
chr1:11991706
|
C | T | 1 | a0001c0001t0001g0156 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.176-849C>T | MFN2 | ENSG00000116688.18 | transcript | ENST00000235329.10 | protein_coding | 3/18 | chr1 | 11991706 | ||||||
chr1:11991780
|
C | T | 1 | a0001c0002t0005g0055 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.176-775C>T | MFN2 | ENSG00000116688.18 | transcript | ENST00000235329.10 | protein_coding | 3/18 | chr1 | 11991780 | ||||||
chr1:11991822
|
G | A | 1 | a0001c0002t0008g0253 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.176-733G>A | MFN2 | ENSG00000116688.18 | transcript | ENST00000235329.10 | protein_coding | 3/18 | chr1 | 11991822 | ||||||
chr1:11991840
|
C | T | 1 | a0001c0001t0002g0067 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.176-715C>T | MFN2 | ENSG00000116688.18 | transcript | ENST00000235329.10 | protein_coding | 3/18 | chr1 | 11991840 | ||||||
chr1:11991841
|
G | A | 1 | a0001c0002t0005g0055 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.176-714G>A | MFN2 | ENSG00000116688.18 | transcript | ENST00000235329.10 | protein_coding | 3/18 | chr1 | 11991841 | ||||||
chr1:11991855
|
C | T | 2 | a0001c0003t0007g0280a0001c0003t0007g0281 | 2 | HG02145.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.176-700C>T | MFN2 | ENSG00000116688.18 | transcript | ENST00000235329.10 | protein_coding | 3/18 | chr1 | 11991855 | ||||||
chr1:11991873
|
C | G | 233 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0009others(230): Show | 269 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(266): Show |
intron_variant | MODIFIER | c.176-682C>G | MFN2 | ENSG00000116688.18 | transcript | ENST00000235329.10 | protein_coding | 3/18 | chr1 | 11991873 | ||||||
chr1:11991910
|
C | A | 12 | a0001c0001t0004g0047a0001c0001t0006g0037a0001c0001t0006g0038others(9): Show | 12 | HG01192.hp2 HG01891.hp2 HG02280.hp1 others(9): Show |
intron_variant | MODIFIER | c.176-645C>A | MFN2 | ENSG00000116688.18 | transcript | ENST00000235329.10 | protein_coding | 3/18 | chr1 | 11991910 | ||||||
chr1:11991923
|
C | CA | 28 | a0001c0001t0001g0008a0001c0001t0001g0084a0001c0001t0002g0008others(25): Show | 33 | HG00140.hp2 HG00280.hp1 HG01123.hp2 others(30): Show |
intron_variant | MODIFIER | c.176-603dupA | MFN2 | ENSG00000116688.18 | transcript | ENST00000235329.10 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr1 | 11991923 | |||||
chr1:11991923
|
C | CAA | 11 | a0001c0001t0001g0029a0001c0001t0001g0163a0001c0001t0001g0168others(8): Show | 12 | HG01243.hp2 HG01891.hp1 HG02109.hp1 others(9): Show |
intron_variant | MODIFIER | c.176-604_176-603dup others(2): Show |
MFN2 | ENSG00000116688.18 | transcript | ENST00000235329.10 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr1 | 11991923 | |||||
chr1:11991923
|
C | CAAA | 46 | a0001c0001t0001g0019a0001c0001t0001g0054a0001c0001t0001g0119others(43): Show | 53 | HG00280.hp2 HG00408.hp2 HG00423.hp1 others(50): Show |
intron_variant | MODIFIER | c.176-605_176-603dup others(3): Show |
MFN2 | ENSG00000116688.18 | transcript | ENST00000235329.10 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr1 | 11991923 | |||||
chr1:11991923
|
C | CAAAA | 31 | a0001c0001t0001g0011a0001c0001t0001g0071a0001c0001t0001g0117others(28): Show | 33 | HG00323.hp2 HG00735.hp1 HG01081.hp2 others(30): Show |
intron_variant | MODIFIER | c.176-606_176-603dup others(4): Show |
MFN2 | ENSG00000116688.18 | transcript | ENST00000235329.10 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr1 | 11991923 | |||||
chr1:11991923
|
C | CAAAAA | 27 | a0001c0001t0001g0004a0001c0001t0001g0010a0001c0001t0001g0013others(24): Show | 38 | HG00558.hp1 HG00597.hp1 HG01123.hp1 others(35): Show |
intron_variant | MODIFIER | c.176-607_176-603dup others(5): Show |
MFN2 | ENSG00000116688.18 | transcript | ENST00000235329.10 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr1 | 11991923 | |||||
chr1:11991923
|
C | CAAAAAA | 38 | a0001c0001t0001g0009a0001c0001t0001g0015a0001c0001t0001g0018others(35): Show | 43 | HG00609.hp1 HG00639.hp1 HG01070.hp1 others(40): Show |
intron_variant | MODIFIER | c.176-608_176-603dup others(6): Show |
MFN2 | ENSG00000116688.18 | transcript | ENST00000235329.10 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr1 | 11991923 | |||||
chr1:11991923
|
C | CAAAAAAA | 17 | a0001c0001t0001g0005a0001c0001t0001g0028a0001c0001t0001g0130others(14): Show | 20 | HG00558.hp2 HG00639.hp2 HG00738.hp2 others(17): Show |
intron_variant | MODIFIER | c.176-609_176-603dup others(7): Show |
MFN2 | ENSG00000116688.18 | transcript | ENST00000235329.10 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr1 | 11991923 | |||||
chr1:11991923
|
C | CAAAAAAA others(1): Show |
8 | a0001c0001t0001g0014a0001c0001t0001g0062a0001c0001t0001g0136others(5): Show | 9 | HG00735.hp2 HG01169.hp2 HG02486.hp1 others(6): Show |
intron_variant | MODIFIER | c.176-610_176-603dup others(8): Show |
MFN2 | ENSG00000116688.18 | transcript | ENST00000235329.10 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr1 | 11991923 | |||||
chr1:11991923
|
C | CAAAAAAA others(2): Show |
9 | a0001c0001t0001g0181a0001c0001t0013g0032a0001c0002t0005g0252others(6): Show | 10 | HG00408.hp1 HG00733.hp2 HG02970.hp2 others(7): Show |
intron_variant | MODIFIER | c.176-611_176-603dup others(9): Show |
MFN2 | ENSG00000116688.18 | transcript | ENST00000235329.10 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr1 | 11991923 | |||||
chr1:11991923
|
C | CAAAAAAA others(3): Show |
9 | a0001c0001t0002g0273a0001c0001t0013g0251a0001c0002t0005g0033others(6): Show | 10 | HG01192.hp1 HG02027.hp1 HG02040.hp2 others(7): Show |
intron_variant | MODIFIER | c.176-612_176-603dup others(10): Show |
MFN2 | ENSG00000116688.18 | transcript | ENST00000235329.10 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr1 | 11991923 | |||||
chr1:11991923
|
C | CAAAAAAA others(4): Show |
1 | a0001c0002t0005g0256 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.176-613_176-603dup others(11): Show |
MFN2 | ENSG00000116688.18 | transcript | ENST00000235329.10 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr1 | 11991923 | |||||
chr1:11991923
|
C | CAAAAAAA others(5): Show |
1 | a0001c0002t0008g0277 | 1 | NA19089.hp2 | intron_variant | MODIFIER | c.176-614_176-603dup others(12): Show |
MFN2 | ENSG00000116688.18 | transcript | ENST00000235329.10 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr1 | 11991923 | |||||
chr1:11991923
|
C | CAAAAAAA others(12): Show |
1 | a0001c0002t0005g0255 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.176-621_176-603dup others(19): Show |
MFN2 | ENSG00000116688.18 | transcript | ENST00000235329.10 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr1 | 11991923 | |||||
chr1:11991923
|
C | CAAAAAAA others(13): Show |
1 | a0001c0002t0005g0254 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.176-622_176-603dup others(20): Show |
MFN2 | ENSG00000116688.18 | transcript | ENST00000235329.10 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr1 | 11991923 | |||||
chr1:11991923
|
CA | C | 20 | a0001c0001t0001g0076a0001c0001t0002g0024a0001c0001t0002g0066others(17): Show | 24 | HG01515.hp2 HG01993.hp1 HG02109.hp2 others(21): Show |
intron_variant | MODIFIER | c.176-603delA | MFN2 | ENSG00000116688.18 | transcript | ENST00000235329.10 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr1 | 11991923 | |||||
chr1:11991923
|
CAAAAAAA others(2): Show |
C | 8 | a0001c0001t0003g0155a0001c0004t0004g0034a0001c0004t0004g0265others(5): Show | 9 | HG02083.hp2 HG03704.hp2 HG04228.hp2 others(6): Show |
intron_variant | MODIFIER | c.176-611_176-603del others(9): Show |
MFN2 | ENSG00000116688.18 | transcript | ENST00000235329.10 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr1 | 11991923 | |||||
chr1:11991923
|
CAAAAAAA others(5): Show |
C | 1 | a0001c0001t0001g0125 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.176-614_176-603del others(12): Show |
MFN2 | ENSG00000116688.18 | transcript | ENST00000235329.10 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr1 | 11991923 | |||||
chr1:11991923
|
CAAAAAAA others(8): Show |
C | 1 | a0001c0001t0004g0047 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.176-617_176-603del others(15): Show |
MFN2 | ENSG00000116688.18 | transcript | ENST00000235329.10 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr1 | 11991923 | |||||
chr1:11992216
|
C | T | 3 | a0001c0001t0003g0188a0001c0001t0003g0245a0001c0001t0003g0250 | 3 | NA18981.hp2 NA19085.hp2 NA19088.hp2 |
intron_variant | MODIFIER | c.176-339C>T | MFN2 | ENSG00000116688.18 | transcript | ENST00000235329.10 | protein_coding | 3/18 | chr1 | 11992216 | ||||||
chr1:11992217
|
G | A | 1 | a0001c0001t0002g0273 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.176-338G>A | MFN2 | ENSG00000116688.18 | transcript | ENST00000235329.10 | protein_coding | 3/18 | chr1 | 11992217 | ||||||
chr1:11992230
|
G | A | 8 | a0001c0004t0004g0034a0001c0004t0004g0265a0001c0004t0004g0267others(5): Show | 9 | HG02083.hp2 HG04228.hp2 NA18952.hp2 others(6): Show |
intron_variant | MODIFIER | c.176-325G>A | MFN2 | ENSG00000116688.18 | transcript | ENST00000235329.10 | protein_coding | 3/18 | chr1 | 11992230 | ||||||
chr1:11992254
|
T | C | 1 | a0001c0001t0001g0132 | 1 | NA18951.hp1 | intron_variant | MODIFIER | c.176-301T>C | MFN2 | ENSG00000116688.18 | transcript | ENST00000235329.10 | protein_coding | 3/18 | chr1 | 11992254 | ||||||
chr1:11992299
|
T | G | 8 | a0001c0004t0004g0034a0001c0004t0004g0265a0001c0004t0004g0267others(5): Show | 9 | HG02083.hp2 HG04228.hp2 NA18952.hp2 others(6): Show |
intron_variant | MODIFIER | c.176-256T>G | MFN2 | ENSG00000116688.18 | transcript | ENST00000235329.10 | protein_coding | 3/18 | chr1 | 11992299 | ||||||
chr1:11992348
|
G | A | 306 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(303): Show | 374 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(371): Show |
intron_variant | MODIFIER | c.176-207G>A | MFN2 | ENSG00000116688.18 | transcript | ENST00000235329.10 | protein_coding | 3/18 | chr1 | 11992348 | ||||||
chr1:11992355
|
G | T | 2 | a0001c0003t0017g0292a0001c0003t0017g0293 | 2 | HG01109.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.176-200G>T | MFN2 | ENSG00000116688.18 | transcript | ENST00000235329.10 | protein_coding | 3/18 | chr1 | 11992355 | ||||||
chr1:11992376
|
C | A | 6 | a0001c0001t0002g0273a0001c0001t0004g0030a0001c0001t0004g0191others(3): Show | 7 | HG02055.hp1 HG02451.hp2 HG02572.hp1 others(4): Show |
intron_variant | MODIFIER | c.176-179C>A | MFN2 | ENSG00000116688.18 | transcript | ENST00000235329.10 | protein_coding | 3/18 | chr1 | 11992376 | ||||||
chr1:11992496
|
C | G | 7 | a0001c0003t0007g0035a0001c0003t0007g0280a0001c0003t0007g0281others(4): Show | 8 | HG01109.hp1 HG01167.hp1 HG02145.hp2 others(5): Show |
intron_variant | MODIFIER | c.176-59C>G | MFN2 | ENSG00000116688.18 | transcript | ENST00000235329.10 | protein_coding | 3/18 | chr1 | 11992496 | ||||||
chr1:11992722
|
T | C | 1 | a0001c0001t0004g0175 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.311+32T>C | MFN2 | ENSG00000116688.18 | transcript | ENST00000235329.10 | protein_coding | 4/18 | chr1 | 11992722 | ||||||
chr1:11992883
|
G | GCCTCGAC others(3): Show |
1 | a0001c0001t0003g0244 | 1 | NA18961.hp2 | intron_variant | MODIFIER | c.311+197_311+206dup others(10): Show |
MFN2 | ENSG00000116688.18 | transcript | ENST00000235329.10 | protein_coding | 4/18 | INFO_REALIGN_3_PRIME | chr1 | 11992883 | |||||
chr1:11992967
|
C | CT | 88 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0076others(85): Show | 123 | HG00140.hp2 HG00323.hp1 HG00423.hp2 others(120): Show |
intron_variant | MODIFIER | c.311+289dupT | MFN2 | ENSG00000116688.18 | transcript | ENST00000235329.10 | protein_coding | 4/18 | INFO_REALIGN_3_PRIME | chr1 | 11992967 | |||||
chr1:11992967
|
C | CTT | 15 | a0001c0002t0005g0033a0001c0002t0005g0055a0001c0002t0005g0190others(12): Show | 17 | HG01109.hp1 HG01167.hp1 HG02027.hp1 others(14): Show |
intron_variant | MODIFIER | c.311+288_311+289dup others(2): Show |
MFN2 | ENSG00000116688.18 | transcript | ENST00000235329.10 | protein_coding | 4/18 | INFO_REALIGN_3_PRIME | chr1 | 11992967 | |||||
chr1:11992967
|
C | CTTT | 30 | a0001c0001t0004g0047a0001c0001t0004g0284a0001c0001t0006g0037others(27): Show | 31 | HG00408.hp1 HG00733.hp2 HG01192.hp1 others(28): Show |
intron_variant | MODIFIER | c.311+287_311+289dup others(3): Show |
MFN2 | ENSG00000116688.18 | transcript | ENST00000235329.10 | protein_coding | 4/18 | INFO_REALIGN_3_PRIME | chr1 | 11992967 | |||||
chr1:11992967
|
C | CTTTT | 73 | a0001c0001t0001g0113a0001c0001t0001g0114a0001c0001t0001g0115others(70): Show | 79 | HG00280.hp2 HG00408.hp2 HG00423.hp1 others(76): Show |
intron_variant | MODIFIER | c.311+286_311+289dup others(4): Show |
MFN2 | ENSG00000116688.18 | transcript | ENST00000235329.10 | protein_coding | 4/18 | INFO_REALIGN_3_PRIME | chr1 | 11992967 | |||||
chr1:11992967
|
C | CTTTTT | 97 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0009others(94): Show | 121 | HG00140.hp1 HG00323.hp2 HG00558.hp1 others(118): Show |
intron_variant | MODIFIER | c.311+285_311+289dup others(5): Show |
MFN2 | ENSG00000116688.18 | transcript | ENST00000235329.10 | protein_coding | 4/18 | INFO_REALIGN_3_PRIME | chr1 | 11992967 | |||||
chr1:11993005
|
A | G | 2 | a0001c0003t0017g0292a0001c0003t0017g0293 | 2 | HG01109.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.311+315A>G | MFN2 | ENSG00000116688.18 | transcript | ENST00000235329.10 | protein_coding | 4/18 | chr1 | 11993005 | ||||||
chr1:11993043
|
C | T | 222 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0009others(219): Show | 256 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(253): Show |
intron_variant | MODIFIER | c.311+353C>T | MFN2 | ENSG00000116688.18 | transcript | ENST00000235329.10 | protein_coding | 4/18 | chr1 | 11993043 | ||||||
chr1:11993068
|
ACCAGTCT others(255): Show |
A | 8 | a0001c0004t0004g0034a0001c0004t0004g0265a0001c0004t0004g0267others(5): Show | 9 | HG02083.hp2 HG04228.hp2 NA18952.hp2 others(6): Show |
intron_variant | MODIFIER | c.311+379_311+640del | MFN2 | ENSG00000116688.18 | transcript | ENST00000235329.10 | protein_coding | 4/18 | chr1 | 11993068 | ||||||
chr1:11993081
|
G | A | 6 | a0001c0001t0001g0010a0001c0001t0001g0128a0001c0001t0001g0131others(3): Show | 9 | HG01258.hp2 HG01346.hp2 HG01943.hp2 others(6): Show |
intron_variant | MODIFIER | c.311+391G>A | MFN2 | ENSG00000116688.18 | transcript | ENST00000235329.10 | protein_coding | 4/18 | chr1 | 11993081 | ||||||
chr1:11993136
|
C | G | 1 | a0001c0002t0005g0259 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.311+446C>G | MFN2 | ENSG00000116688.18 | transcript | ENST00000235329.10 | protein_coding | 4/18 | chr1 | 11993136 | ||||||
chr1:11993171
|
TCTA | T | 4 | a0001c0001t0003g0219a0001c0001t0003g0226a0001c0001t0003g0232others(1): Show | 4 | HG02129.hp2 NA18957.hp1 NA19003.hp1 others(1): Show |
intron_variant | MODIFIER | c.311+484_311+486del others(3): Show |
MFN2 | ENSG00000116688.18 | transcript | ENST00000235329.10 | protein_coding | 4/18 | INFO_REALIGN_3_PRIME | chr1 | 11993171 | |||||
chr1:11993207
|
T | C | 206 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0009others(203): Show | 238 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(235): Show |
intron_variant | MODIFIER | c.311+517T>C | MFN2 | ENSG00000116688.18 | transcript | ENST00000235329.10 | protein_coding | 4/18 | chr1 | 11993207 | ||||||
chr1:11993334
|
G | A | 10 | a0001c0001t0004g0016a0001c0001t0004g0195a0001c0001t0004g0196others(7): Show | 12 | HG02280.hp2 HG02572.hp2 HG02622.hp1 others(9): Show |
intron_variant | MODIFIER | c.311+644G>A | MFN2 | ENSG00000116688.18 | transcript | ENST00000235329.10 | protein_coding | 4/18 | chr1 | 11993334 | ||||||
chr1:11993418
|
C | CA | 9 | a0001c0001t0001g0093a0001c0001t0002g0092a0001c0003t0007g0035others(6): Show | 10 | HG01109.hp1 HG01167.hp1 HG01255.hp1 others(7): Show |
intron_variant | MODIFIER | c.311+737dupA | MFN2 | ENSG00000116688.18 | transcript | ENST00000235329.10 | protein_coding | 4/18 | INFO_REALIGN_3_PRIME | chr1 | 11993418 | |||||
chr1:11993644
|
AGAATGGT others(2): Show |
A | 8 | a0001c0004t0004g0034a0001c0004t0004g0265a0001c0004t0004g0267others(5): Show | 9 | HG02083.hp2 HG04228.hp2 NA18952.hp2 others(6): Show |
intron_variant | MODIFIER | c.311+958_311+966del others(9): Show |
MFN2 | ENSG00000116688.18 | transcript | ENST00000235329.10 | protein_coding | 4/18 | INFO_REALIGN_3_PRIME | chr1 | 11993644 | |||||
chr1:11993660
|
C | CG | 7 | a0001c0003t0007g0035a0001c0003t0007g0280a0001c0003t0007g0281others(4): Show | 8 | HG01109.hp1 HG01167.hp1 HG02145.hp2 others(5): Show |
intron_variant | MODIFIER | c.311+970_311+971ins others(1): Show |
MFN2 | ENSG00000116688.18 | transcript | ENST00000235329.10 | protein_coding | 4/18 | chr1 | 11993660 | ||||||
chr1:11993661
|
A | G | 222 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0009others(219): Show | 256 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(253): Show |
intron_variant | MODIFIER | c.311+971A>G | MFN2 | ENSG00000116688.18 | transcript | ENST00000235329.10 | protein_coding | 4/18 | chr1 | 11993661 | ||||||
chr1:11993668
|
G | A | 8 | a0001c0004t0004g0034a0001c0004t0004g0265a0001c0004t0004g0267others(5): Show | 9 | HG02083.hp2 HG04228.hp2 NA18952.hp2 others(6): Show |
intron_variant | MODIFIER | c.311+978G>A | MFN2 | ENSG00000116688.18 | transcript | ENST00000235329.10 | protein_coding | 4/18 | chr1 | 11993668 | ||||||
chr1:11993733
|
C | CA | 6 | a0001c0001t0002g0068a0001c0001t0002g0069a0001c0001t0002g0085others(3): Show | 6 | HG01346.hp1 HG03516.hp1 NA18947.hp1 others(3): Show |
intron_variant | MODIFIER | c.311+1060dupA | MFN2 | ENSG00000116688.18 | transcript | ENST00000235329.10 | protein_coding | 4/18 | INFO_REALIGN_3_PRIME | chr1 | 11993733 | |||||
chr1:11993733
|
CA | C | 208 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0009others(205): Show | 241 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(238): Show |
intron_variant | MODIFIER | c.311+1060delA | MFN2 | ENSG00000116688.18 | transcript | ENST00000235329.10 | protein_coding | 4/18 | INFO_REALIGN_3_PRIME | chr1 | 11993733 | |||||
chr1:11993733
|
CAAAAA | C | 7 | a0001c0004t0004g0034a0001c0004t0004g0265a0001c0004t0004g0269others(4): Show | 8 | HG02083.hp2 HG04228.hp2 NA18952.hp2 others(5): Show |
intron_variant | MODIFIER | c.311+1056_311+1060d others(7): Show |
MFN2 | ENSG00000116688.18 | transcript | ENST00000235329.10 | protein_coding | 4/18 | INFO_REALIGN_3_PRIME | chr1 | 11993733 | |||||
chr1:11993774
|
T | G | 2 | a0001c0002t0005g0257a0001c0002t0005g0259 | 2 | HG03017.hp2 HG03654.hp2 |
intron_variant | MODIFIER | c.311+1084T>G | MFN2 | ENSG00000116688.18 | transcript | ENST00000235329.10 | protein_coding | 4/18 | chr1 | 11993774 | ||||||
chr1:11993826
|
T | C | 1 | a0001c0001t0003g0211 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.311+1136T>C | MFN2 | ENSG00000116688.18 | transcript | ENST00000235329.10 | protein_coding | 4/18 | chr1 | 11993826 | ||||||
chr1:11993865
|
G | A | 15 | a0001c0003t0007g0035a0001c0003t0007g0280a0001c0003t0007g0281others(12): Show | 17 | HG01109.hp1 HG01167.hp1 HG02083.hp2 others(14): Show |
intron_variant | MODIFIER | c.311+1175G>A | MFN2 | ENSG00000116688.18 | transcript | ENST00000235329.10 | protein_coding | 4/18 | chr1 | 11993865 | ||||||
chr1:11993940
|
G | A | 7 | a0001c0003t0007g0035a0001c0003t0007g0280a0001c0003t0007g0281others(4): Show | 8 | HG01109.hp1 HG01167.hp1 HG02145.hp2 others(5): Show |
intron_variant | MODIFIER | c.311+1250G>A | MFN2 | ENSG00000116688.18 | transcript | ENST00000235329.10 | protein_coding | 4/18 | chr1 | 11993940 | ||||||
chr1:11993973
|
G | A | 232 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0009others(229): Show | 268 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(265): Show |
intron_variant | MODIFIER | c.311+1283G>A | MFN2 | ENSG00000116688.18 | transcript | ENST00000235329.10 | protein_coding | 4/18 | chr1 | 11993973 | ||||||
chr1:11994025
|
G | A | 1 | a0001c0001t0006g0040 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.311+1335G>A | MFN2 | ENSG00000116688.18 | transcript | ENST00000235329.10 | protein_coding | 4/18 | chr1 | 11994025 | ||||||
chr1:11994244
|
C | G | 4 | a0001c0001t0004g0030a0001c0001t0004g0191a0001c0001t0004g0192others(1): Show | 5 | HG02572.hp1 HG02818.hp2 HG02886.hp1 others(2): Show |
intron_variant | MODIFIER | c.311+1554C>G | MFN2 | ENSG00000116688.18 | transcript | ENST00000235329.10 | protein_coding | 4/18 | chr1 | 11994244 | ||||||
chr1:11994264
|
A | G | 1 | a0001c0001t0002g0068 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.311+1574A>G | MFN2 | ENSG00000116688.18 | transcript | ENST00000235329.10 | protein_coding | 4/18 | chr1 | 11994264 | ||||||
chr1:11994302
|
A | G | 1 | a0001c0001t0001g0142 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.311+1612A>G | MFN2 | ENSG00000116688.18 | transcript | ENST00000235329.10 | protein_coding | 4/18 | chr1 | 11994302 | ||||||
chr1:11994331
|
G | C | 6 | a0001c0001t0004g0296a0001c0001t0004g0297a0001c0001t0004g0298others(3): Show | 6 | HG02630.hp2 HG02895.hp2 HG03195.hp2 others(3): Show |
intron_variant | MODIFIER | c.311+1641G>C | MFN2 | ENSG00000116688.18 | transcript | ENST00000235329.10 | protein_coding | 4/18 | chr1 | 11994331 | ||||||
chr1:11994463
|
G | A | 2 | a0001c0001t0001g0137a0004c0011t0001g0180 | 2 | NA18960.hp1 NA18993.hp2 |
intron_variant | MODIFIER | c.312-1693G>A | MFN2 | ENSG00000116688.18 | transcript | ENST00000235329.10 | protein_coding | 4/18 | chr1 | 11994463 | ||||||
chr1:11994507
|
A | G | 1 | a0001c0001t0001g0164 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.312-1649A>G | MFN2 | ENSG00000116688.18 | transcript | ENST00000235329.10 | protein_coding | 4/18 | chr1 | 11994507 | ||||||
chr1:11994538
|
C | G | 2 | a0001c0001t0001g0072a0001c0001t0001g0074 | 2 | HG00639.hp1 HG04204.hp2 |
intron_variant | MODIFIER | c.312-1618C>G | MFN2 | ENSG00000116688.18 | transcript | ENST00000235329.10 | protein_coding | 4/18 | chr1 | 11994538 | ||||||
chr1:11994583
|
C | G | 1 | a0001c0001t0001g0286 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.312-1573C>G | MFN2 | ENSG00000116688.18 | transcript | ENST00000235329.10 | protein_coding | 4/18 | chr1 | 11994583 | ||||||
chr1:11994584
|
C | T | 7 | a0001c0003t0007g0035a0001c0003t0007g0280a0001c0003t0007g0281others(4): Show | 8 | HG01109.hp1 HG01167.hp1 HG02145.hp2 others(5): Show |
intron_variant | MODIFIER | c.312-1572C>T | MFN2 | ENSG00000116688.18 | transcript | ENST00000235329.10 | protein_coding | 4/18 | chr1 | 11994584 | ||||||
chr1:11994589
|
C | CA | 7 | a0001c0004t0004g0034a0001c0004t0004g0265a0001c0004t0004g0267others(4): Show | 8 | HG02083.hp2 HG04228.hp2 NA18952.hp2 others(5): Show |
intron_variant | MODIFIER | c.312-1555dupA | MFN2 | ENSG00000116688.18 | transcript | ENST00000235329.10 | protein_coding | 4/18 | INFO_REALIGN_3_PRIME | chr1 | 11994589 | |||||
chr1:11994615
|
A | G | 10 | a0001c0001t0004g0016a0001c0001t0004g0195a0001c0001t0004g0196others(7): Show | 12 | HG02280.hp2 HG02572.hp2 HG02622.hp1 others(9): Show |
intron_variant | MODIFIER | c.312-1541A>G | MFN2 | ENSG00000116688.18 | transcript | ENST00000235329.10 | protein_coding | 4/18 | chr1 | 11994615 | ||||||
chr1:11994691
|
C | A | 2 | a0001c0001t0010g0020a0001c0001t0010g0099 | 3 | HG02257.hp2 HG02818.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.312-1465C>A | MFN2 | ENSG00000116688.18 | transcript | ENST00000235329.10 | protein_coding | 4/18 | chr1 | 11994691 | ||||||
chr1:11994854
|
A | G | 222 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0009others(219): Show | 256 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(253): Show |
intron_variant | MODIFIER | c.312-1302A>G | MFN2 | ENSG00000116688.18 | transcript | ENST00000235329.10 | protein_coding | 4/18 | chr1 | 11994854 | ||||||
chr1:11995165
|
G | A | 1 | a0001c0001t0016g0086 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.312-991G>A | MFN2 | ENSG00000116688.18 | transcript | ENST00000235329.10 | protein_coding | 4/18 | chr1 | 11995165 | ||||||
chr1:11995357
|
G | A | 5 | a0001c0003t0007g0035a0001c0003t0007g0280a0001c0003t0007g0281others(2): Show | 6 | HG01167.hp1 HG02145.hp2 HG02622.hp2 others(3): Show |
intron_variant | MODIFIER | c.312-799G>A | MFN2 | ENSG00000116688.18 | transcript | ENST00000235329.10 | protein_coding | 4/18 | chr1 | 11995357 | ||||||
chr1:11995398
|
T | C | 8 | a0001c0004t0004g0034a0001c0004t0004g0265a0001c0004t0004g0267others(5): Show | 9 | HG02083.hp2 HG04228.hp2 NA18952.hp2 others(6): Show |
intron_variant | MODIFIER | c.312-758T>C | MFN2 | ENSG00000116688.18 | transcript | ENST00000235329.10 | protein_coding | 4/18 | chr1 | 11995398 | ||||||
chr1:11995406
|
G | A | 7 | a0001c0003t0007g0035a0001c0003t0007g0280a0001c0003t0007g0281others(4): Show | 8 | HG01109.hp1 HG01167.hp1 HG02145.hp2 others(5): Show |
intron_variant | MODIFIER | c.312-750G>A | MFN2 | ENSG00000116688.18 | transcript | ENST00000235329.10 | protein_coding | 4/18 | chr1 | 11995406 | ||||||
chr1:11995432
|
C | A | 8 | a0001c0004t0004g0034a0001c0004t0004g0265a0001c0004t0004g0267others(5): Show | 9 | HG02083.hp2 HG04228.hp2 NA18952.hp2 others(6): Show |
intron_variant | MODIFIER | c.312-724C>A | MFN2 | ENSG00000116688.18 | transcript | ENST00000235329.10 | protein_coding | 4/18 | chr1 | 11995432 | ||||||
chr1:11995642
|
T | TA | 7 | a0001c0003t0007g0035a0001c0003t0007g0280a0001c0003t0007g0281others(4): Show | 8 | HG01109.hp1 HG01167.hp1 HG02145.hp2 others(5): Show |
intron_variant | MODIFIER | c.312-503dupA | MFN2 | ENSG00000116688.18 | transcript | ENST00000235329.10 | protein_coding | 4/18 | INFO_REALIGN_3_PRIME | chr1 | 11995642 | |||||
chr1:11995643
|
A | G | 8 | a0001c0004t0004g0034a0001c0004t0004g0265a0001c0004t0004g0267others(5): Show | 9 | HG02083.hp2 HG04228.hp2 NA18952.hp2 others(6): Show |
intron_variant | MODIFIER | c.312-513A>G | MFN2 | ENSG00000116688.18 | transcript | ENST00000235329.10 | protein_coding | 4/18 | chr1 | 11995643 | ||||||
chr1:11995665
|
T | G | 1 | a0001c0001t0002g0064 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.312-491T>G | MFN2 | ENSG00000116688.18 | transcript | ENST00000235329.10 | protein_coding | 4/18 | chr1 | 11995665 | ||||||
chr1:11995706
|
A | G | 2 | a0001c0001t0004g0016a0001c0001t0004g0197 | 4 | HG02280.hp2 HG02572.hp2 HG02622.hp1 others(1): Show |
intron_variant | MODIFIER | c.312-450A>G | MFN2 | ENSG00000116688.18 | transcript | ENST00000235329.10 | protein_coding | 4/18 | chr1 | 11995706 | ||||||
chr1:11995917
|
C | T | 2 | a0001c0001t0001g0054a0001c0001t0004g0284 | 2 | HG02615.hp1 HG02965.hp1 |
intron_variant | MODIFIER | c.312-239C>T | MFN2 | ENSG00000116688.18 | transcript | ENST00000235329.10 | protein_coding | 4/18 | chr1 | 11995917 | ||||||
chr1:11996010
|
T | C | 8 | a0001c0004t0004g0034a0001c0004t0004g0265a0001c0004t0004g0267others(5): Show | 9 | HG02083.hp2 HG04228.hp2 NA18952.hp2 others(6): Show |
intron_variant | MODIFIER | c.312-146T>C | MFN2 | ENSG00000116688.18 | transcript | ENST00000235329.10 | protein_coding | 4/18 | chr1 | 11996010 | ||||||
chr1:11996018
|
C | G | 12 | a0001c0001t0004g0047a0001c0001t0006g0037a0001c0001t0006g0038others(9): Show | 12 | HG01192.hp2 HG01891.hp2 HG02280.hp1 others(9): Show |
intron_variant | MODIFIER | c.312-138C>G | MFN2 | ENSG00000116688.18 | transcript | ENST00000235329.10 | protein_coding | 4/18 | chr1 | 11996018 | ||||||
chr1:11996383
|
C | T | 214 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0009others(211): Show | 247 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(244): Show |
intron_variant | MODIFIER | c.474+65C>T | MFN2 | ENSG00000116688.18 | transcript | ENST00000235329.10 | protein_coding | 5/18 | chr1 | 11996383 | ||||||
chr1:11996404
|
A | C | 3 | a0001c0001t0015g0050a0001c0001t0015g0051a0001c0001t0015g0053 | 3 | HG02559.hp1 HG02723.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.474+86A>C | MFN2 | ENSG00000116688.18 | transcript | ENST00000235329.10 | protein_coding | 5/18 | chr1 | 11996404 | ||||||
chr1:11996406
|
G | C | 2 | a0001c0005t0004g0122a0001c0005t0004g0295 | 2 | HG03195.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.474+88G>C | MFN2 | ENSG00000116688.18 | transcript | ENST00000235329.10 | protein_coding | 5/18 | chr1 | 11996406 | ||||||
chr1:11996596
|
A | G | 7 | a0001c0003t0007g0035a0001c0003t0007g0280a0001c0003t0007g0281others(4): Show | 8 | HG01109.hp1 HG01167.hp1 HG02145.hp2 others(5): Show |
intron_variant | MODIFIER | c.474+278A>G | MFN2 | ENSG00000116688.18 | transcript | ENST00000235329.10 | protein_coding | 5/18 | chr1 | 11996596 | ||||||
chr1:11996678
|
G | A | 3 | a0001c0001t0003g0189a0001c0001t0003g0209a0001c0001t0003g0227 | 3 | HG03688.hp1 HG03710.hp2 HG04184.hp2 |
intron_variant | MODIFIER | c.474+360G>A | MFN2 | ENSG00000116688.18 | transcript | ENST00000235329.10 | protein_coding | 5/18 | chr1 | 11996678 | ||||||
chr1:11996725
|
G | C | 2 | a0001c0001t0002g0082a0001c0001t0002g0087 | 2 | HG02074.hp2 NA18995.hp2 |
intron_variant | MODIFIER | c.474+407G>C | MFN2 | ENSG00000116688.18 | transcript | ENST00000235329.10 | protein_coding | 5/18 | chr1 | 11996725 | ||||||
chr1:11996758
|
T | C | 304 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(301): Show | 372 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(369): Show |
intron_variant | MODIFIER | c.474+440T>C | MFN2 | ENSG00000116688.18 | transcript | ENST00000235329.10 | protein_coding | 5/18 | chr1 | 11996758 | ||||||
chr1:11996760
|
G | C | 1 | a0001c0002t0008g0278 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.474+442G>C | MFN2 | ENSG00000116688.18 | transcript | ENST00000235329.10 | protein_coding | 5/18 | chr1 | 11996760 | ||||||
chr1:11996888
|
A | C | 214 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0009others(211): Show | 247 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(244): Show |
intron_variant | MODIFIER | c.475-409A>C | MFN2 | ENSG00000116688.18 | transcript | ENST00000235329.10 | protein_coding | 5/18 | chr1 | 11996888 | ||||||
chr1:11997025
|
C | T | 1 | a0001c0001t0003g0240 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.475-272C>T | MFN2 | ENSG00000116688.18 | transcript | ENST00000235329.10 | protein_coding | 5/18 | chr1 | 11997025 | ||||||
chr1:11997026
|
G | A | 1 | a0001c0001t0003g0223 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.475-271G>A | MFN2 | ENSG00000116688.18 | transcript | ENST00000235329.10 | protein_coding | 5/18 | chr1 | 11997026 | ||||||
chr1:11997038
|
C | CA | 8 | a0001c0001t0002g0012a0001c0001t0002g0094a0001c0001t0002g0110others(5): Show | 9 | HG01175.hp2 HG02280.hp1 HG02630.hp2 others(6): Show |
intron_variant | MODIFIER | c.475-240dupA | MFN2 | ENSG00000116688.18 | transcript | ENST00000235329.10 | protein_coding | 5/18 | INFO_REALIGN_3_PRIME | chr1 | 11997038 | |||||
chr1:11997038
|
CA | C | 206 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0009others(203): Show | 239 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(236): Show |
intron_variant | MODIFIER | c.475-240delA | MFN2 | ENSG00000116688.18 | transcript | ENST00000235329.10 | protein_coding | 5/18 | INFO_REALIGN_3_PRIME | chr1 | 11997038 | |||||
chr1:11997038
|
CAA | C | 7 | a0001c0001t0001g0173a0001c0001t0004g0048a0001c0001t0004g0129others(4): Show | 7 | HG01884.hp2 HG02886.hp2 HG02896.hp1 others(4): Show |
intron_variant | MODIFIER | c.475-241_475-240del others(2): Show |
MFN2 | ENSG00000116688.18 | transcript | ENST00000235329.10 | protein_coding | 5/18 | INFO_REALIGN_3_PRIME | chr1 | 11997038 | |||||
chr1:11997065
|
T | G | 5 | a0001c0003t0007g0035a0001c0003t0007g0280a0001c0003t0007g0281others(2): Show | 6 | HG01167.hp1 HG02145.hp2 HG02622.hp2 others(3): Show |
intron_variant | MODIFIER | c.475-232T>G | MFN2 | ENSG00000116688.18 | transcript | ENST00000235329.10 | protein_coding | 5/18 | chr1 | 11997065 | ||||||
chr1:11997101
|
G | A | 1 | a0001c0001t0001g0288 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.475-196G>A | MFN2 | ENSG00000116688.18 | transcript | ENST00000235329.10 | protein_coding | 5/18 | chr1 | 11997101 | ||||||
chr1:11997230
|
C | G | 2 | a0001c0002t0008g0262a0005c0015t0008g0258 | 2 | NA19068.hp1 NA19080.hp1 |
intron_variant | MODIFIER | c.475-67C>G | MFN2 | ENSG00000116688.18 | transcript | ENST00000235329.10 | protein_coding | 5/18 | chr1 | 11997230 | ||||||
chr1:11997254
|
G | C | 1 | a0001c0001t0006g0037 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.475-43G>C | MFN2 | ENSG00000116688.18 | transcript | ENST00000235329.10 | protein_coding | 5/18 | chr1 | 11997254 | ||||||
chr1:11997264
|
C | T | 8 | a0001c0004t0004g0034a0001c0004t0004g0265a0001c0004t0004g0267others(5): Show | 9 | HG02083.hp2 HG04228.hp2 NA18952.hp2 others(6): Show |
intron_variant | MODIFIER | c.475-33C>T | MFN2 | ENSG00000116688.18 | transcript | ENST00000235329.10 | protein_coding | 5/18 | chr1 | 11997264 | ||||||
chr1:11997525
|
T | A | 1 | a0001c0001t0026g0272 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.599+104T>A | MFN2 | ENSG00000116688.18 | transcript | ENST00000235329.10 | protein_coding | 6/18 | chr1 | 11997525 | ||||||
chr1:11997530
|
A | G | 2 | a0001c0003t0017g0292a0001c0003t0017g0293 | 2 | HG01109.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.599+109A>G | MFN2 | ENSG00000116688.18 | transcript | ENST00000235329.10 | protein_coding | 6/18 | chr1 | 11997530 | ||||||
chr1:11997536
|
A | C | 7 | a0001c0003t0007g0035a0001c0003t0007g0280a0001c0003t0007g0281others(4): Show | 8 | HG01109.hp1 HG01167.hp1 HG02145.hp2 others(5): Show |
intron_variant | MODIFIER | c.599+115A>C | MFN2 | ENSG00000116688.18 | transcript | ENST00000235329.10 | protein_coding | 6/18 | chr1 | 11997536 | ||||||
chr1:11997675
|
G | A | 3 | a0001c0001t0016g0086a0001c0001t0016g0088a0001c0001t0019g0107 | 3 | HG02698.hp1 HG03710.hp1 HG03942.hp2 |
intron_variant | MODIFIER | c.599+254G>A | MFN2 | ENSG00000116688.18 | transcript | ENST00000235329.10 | protein_coding | 6/18 | chr1 | 11997675 | ||||||
chr1:11997736
|
G | C | 1 | a0001c0003t0017g0292 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.599+315G>C | MFN2 | ENSG00000116688.18 | transcript | ENST00000235329.10 | protein_coding | 6/18 | chr1 | 11997736 | ||||||
chr1:11997853
|
A | C | 1 | a0001c0001t0002g0102 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.599+432A>C | MFN2 | ENSG00000116688.18 | transcript | ENST00000235329.10 | protein_coding | 6/18 | chr1 | 11997853 | ||||||
chr1:11997856
|
A | C | 1 | a0001c0001t0002g0102 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.599+435A>C | MFN2 | ENSG00000116688.18 | transcript | ENST00000235329.10 | protein_coding | 6/18 | chr1 | 11997856 | ||||||
chr1:11997879
|
C | CT | 23 | a0001c0001t0002g0059a0001c0001t0002g0083a0001c0001t0004g0016others(20): Show | 26 | HG01884.hp2 HG02083.hp2 HG02280.hp2 others(23): Show |
intron_variant | MODIFIER | c.599+480dupT | MFN2 | ENSG00000116688.18 | transcript | ENST00000235329.10 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr1 | 11997879 | |||||
chr1:11997879
|
C | CTTT | 164 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0009others(161): Show | 195 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(192): Show |
intron_variant | MODIFIER | c.599+478_599+480dup others(3): Show |
MFN2 | ENSG00000116688.18 | transcript | ENST00000235329.10 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr1 | 11997879 | |||||
chr1:11997879
|
C | CTTTT | 12 | a0001c0001t0001g0019a0001c0001t0001g0141a0001c0001t0001g0153others(9): Show | 13 | HG00597.hp1 HG00738.hp1 HG00741.hp1 others(10): Show |
intron_variant | MODIFIER | c.599+477_599+480dup others(4): Show |
MFN2 | ENSG00000116688.18 | transcript | ENST00000235329.10 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr1 | 11997879 | |||||
chr1:11997879
|
CT | C | 6 | a0001c0001t0002g0095a0001c0001t0002g0289a0001c0003t0007g0035others(3): Show | 7 | HG01070.hp2 HG01167.hp1 HG02622.hp2 others(4): Show |
intron_variant | MODIFIER | c.599+480delT | MFN2 | ENSG00000116688.18 | transcript | ENST00000235329.10 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr1 | 11997879 | |||||
chr1:11997914
|
T | C | 1 | a0001c0001t0001g0186 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.599+493T>C | MFN2 | ENSG00000116688.18 | transcript | ENST00000235329.10 | protein_coding | 6/18 | chr1 | 11997914 | ||||||
chr1:11997915
|
G | A | 1 | a0001c0001t0001g0186 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.599+494G>A | MFN2 | ENSG00000116688.18 | transcript | ENST00000235329.10 | protein_coding | 6/18 | chr1 | 11997915 | ||||||
chr1:11997917
|
T | C | 12 | a0001c0001t0004g0047a0001c0001t0006g0037a0001c0001t0006g0038others(9): Show | 12 | HG01192.hp2 HG01891.hp2 HG02280.hp1 others(9): Show |
intron_variant | MODIFIER | c.599+496T>C | MFN2 | ENSG00000116688.18 | transcript | ENST00000235329.10 | protein_coding | 6/18 | chr1 | 11997917 | ||||||
chr1:11997952
|
C | T | 1 | a0001c0001t0004g0194 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.599+531C>T | MFN2 | ENSG00000116688.18 | transcript | ENST00000235329.10 | protein_coding | 6/18 | chr1 | 11997952 | ||||||
chr1:11997989
|
T | C | 1 | a0001c0002t0005g0259 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.599+568T>C | MFN2 | ENSG00000116688.18 | transcript | ENST00000235329.10 | protein_coding | 6/18 | chr1 | 11997989 | ||||||
chr1:11998028
|
T | C | 1 | a0001c0001t0001g0286 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.599+607T>C | MFN2 | ENSG00000116688.18 | transcript | ENST00000235329.10 | protein_coding | 6/18 | chr1 | 11998028 | ||||||
chr1:11998029
|
G | A | 1 | a0001c0001t0001g0286 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.599+608G>A | MFN2 | ENSG00000116688.18 | transcript | ENST00000235329.10 | protein_coding | 6/18 | chr1 | 11998029 | ||||||
chr1:11998031
|
C | A | 1 | a0001c0001t0001g0286 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.599+610C>A | MFN2 | ENSG00000116688.18 | transcript | ENST00000235329.10 | protein_coding | 6/18 | chr1 | 11998031 | ||||||
chr1:11998072
|
C | T | 1 | a0001c0001t0001g0203 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.599+651C>T | MFN2 | ENSG00000116688.18 | transcript | ENST00000235329.10 | protein_coding | 6/18 | chr1 | 11998072 | ||||||
chr1:11998111
|
T | C | 1 | a0001c0001t0001g0143 | 1 | HG01258.hp2 | intron_variant | MODIFIER | c.600-659T>C | MFN2 | ENSG00000116688.18 | transcript | ENST00000235329.10 | protein_coding | 6/18 | chr1 | 11998111 | ||||||
chr1:11998118
|
A | G | 5 | a0001c0001t0001g0114a0001c0001t0001g0287a0001c0001t0002g0112others(2): Show | 5 | HG02257.hp1 HG02559.hp1 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.600-652A>G | MFN2 | ENSG00000116688.18 | transcript | ENST00000235329.10 | protein_coding | 6/18 | chr1 | 11998118 | ||||||
chr1:11998134
|
A | G | 56 | a0001c0001t0001g0153a0001c0001t0001g0170a0001c0001t0001g0212others(53): Show | 63 | HG00280.hp2 HG00408.hp2 HG00423.hp1 others(60): Show |
intron_variant | MODIFIER | c.600-636A>G | MFN2 | ENSG00000116688.18 | transcript | ENST00000235329.10 | protein_coding | 6/18 | chr1 | 11998134 | ||||||
chr1:11998158
|
G | A | 1 | a0001c0001t0002g0104 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.600-612G>A | MFN2 | ENSG00000116688.18 | transcript | ENST00000235329.10 | protein_coding | 6/18 | chr1 | 11998158 | ||||||
chr1:11998162
|
A | G | 1 | a0001c0001t0002g0104 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.600-608A>G | MFN2 | ENSG00000116688.18 | transcript | ENST00000235329.10 | protein_coding | 6/18 | chr1 | 11998162 | ||||||
chr1:11998173
|
T | C | 2 | a0001c0001t0002g0273a0001c0001t0004g0100 | 2 | HG02055.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.600-597T>C | MFN2 | ENSG00000116688.18 | transcript | ENST00000235329.10 | protein_coding | 6/18 | chr1 | 11998173 | ||||||
chr1:11998480
|
G | A | 1 | a0001c0001t0001g0134 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.600-290G>A | MFN2 | ENSG00000116688.18 | transcript | ENST00000235329.10 | protein_coding | 6/18 | chr1 | 11998480 | ||||||
chr1:11998497
|
G | A | 1 | a0001c0001t0001g0117 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.600-273G>A | MFN2 | ENSG00000116688.18 | transcript | ENST00000235329.10 | protein_coding | 6/18 | chr1 | 11998497 | ||||||
chr1:11998523
|
G | A | 12 | a0001c0001t0004g0047a0001c0001t0006g0037a0001c0001t0006g0038others(9): Show | 12 | HG01192.hp2 HG01891.hp2 HG02280.hp1 others(9): Show |
intron_variant | MODIFIER | c.600-247G>A | MFN2 | ENSG00000116688.18 | transcript | ENST00000235329.10 | protein_coding | 6/18 | chr1 | 11998523 | ||||||
chr1:11998549
|
AAAAAC | A | 219 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0009others(216): Show | 254 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(251): Show |
intron_variant | MODIFIER | c.600-199_600-195del others(5): Show |
MFN2 | ENSG00000116688.18 | transcript | ENST00000235329.10 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr1 | 11998549 | |||||
chr1:11998654
|
G | A | 1 | a0001c0001t0001g0028 | 2 | HG01069.hp1 HG01071.hp1 |
intron_variant | MODIFIER | c.600-116G>A | MFN2 | ENSG00000116688.18 | transcript | ENST00000235329.10 | protein_coding | 6/18 | chr1 | 11998654 | ||||||
chr1:11998685
|
C | T | 8 | a0001c0001t0001g0237a0001c0001t0003g0031a0001c0001t0003g0218others(5): Show | 8 | NA18946.hp1 NA18952.hp1 NA18967.hp1 others(5): Show |
intron_variant | MODIFIER | c.600-85C>T | MFN2 | ENSG00000116688.18 | transcript | ENST00000235329.10 | protein_coding | 6/18 | chr1 | 11998685 | ||||||
chr1:11998745
|
T | C | 28 | a0001c0002t0005g0033a0001c0002t0005g0055a0001c0002t0005g0089others(25): Show | 30 | HG00408.hp1 HG00733.hp2 HG01192.hp1 others(27): Show |
intron_variant | MODIFIER | c.600-25T>C | MFN2 | ENSG00000116688.18 | transcript | ENST00000235329.10 | protein_coding | 6/18 | chr1 | 11998745 | ||||||
chr1:11998936
|
G | A | 1 | a0001c0001t0001g0288 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.709-52G>A | MFN2 | ENSG00000116688.18 | transcript | ENST00000235329.10 | protein_coding | 7/18 | chr1 | 11998936 | ||||||
chr1:11998953
|
G | A | 1 | a0001c0001t0003g0235 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.709-35G>A | MFN2 | ENSG00000116688.18 | transcript | ENST00000235329.10 | protein_coding | 7/18 | chr1 | 11998953 | ||||||
chr1:11999303
|
C | T | 1 | a0001c0001t0001g0119 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.816+208C>T | MFN2 | ENSG00000116688.18 | transcript | ENST00000235329.10 | protein_coding | 8/18 | chr1 | 11999303 | ||||||
chr1:11999355
|
C | T | 101 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0009others(98): Show | 125 | HG00140.hp1 HG00280.hp1 HG00323.hp2 others(122): Show |
intron_variant | MODIFIER | c.816+260C>T | MFN2 | ENSG00000116688.18 | transcript | ENST00000235329.10 | protein_coding | 8/18 | chr1 | 11999355 | ||||||
chr1:11999441
|
G | A | 28 | a0001c0002t0005g0033a0001c0002t0005g0055a0001c0002t0005g0089others(25): Show | 30 | HG00408.hp1 HG00733.hp2 HG01192.hp1 others(27): Show |
intron_variant | MODIFIER | c.816+346G>A | MFN2 | ENSG00000116688.18 | transcript | ENST00000235329.10 | protein_coding | 8/18 | chr1 | 11999441 | ||||||
chr1:11999491
|
A | G | 21 | a0001c0002t0005g0033a0001c0002t0005g0055a0001c0002t0005g0089others(18): Show | 22 | HG00408.hp1 HG00733.hp2 HG01192.hp1 others(19): Show |
intron_variant | MODIFIER | c.816+396A>G | MFN2 | ENSG00000116688.18 | transcript | ENST00000235329.10 | protein_coding | 8/18 | chr1 | 11999491 | ||||||
chr1:11999546
|
C | T | 1 | a0001c0001t0004g0194 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.816+451C>T | MFN2 | ENSG00000116688.18 | transcript | ENST00000235329.10 | protein_coding | 8/18 | chr1 | 11999546 | ||||||
chr1:11999689
|
C | T | 2 | a0001c0001t0001g0141a0001c0001t0001g0149 | 2 | HG01515.hp1 HG01517.hp1 |
intron_variant | MODIFIER | c.816+594C>T | MFN2 | ENSG00000116688.18 | transcript | ENST00000235329.10 | protein_coding | 8/18 | chr1 | 11999689 | ||||||
chr1:11999726
|
A | G | 5 | a0001c0003t0007g0035a0001c0003t0007g0280a0001c0003t0007g0281others(2): Show | 6 | HG01167.hp1 HG02145.hp2 HG02622.hp2 others(3): Show |
intron_variant | MODIFIER | c.816+631A>G | MFN2 | ENSG00000116688.18 | transcript | ENST00000235329.10 | protein_coding | 8/18 | chr1 | 11999726 | ||||||
chr1:11999810
|
G | A | 4 | a0001c0001t0012g0036a0001c0001t0012g0302a0001c0001t0013g0032others(1): Show | 6 | HG02109.hp2 HG02145.hp1 HG02970.hp2 others(3): Show |
intron_variant | MODIFIER | c.816+715G>A | MFN2 | ENSG00000116688.18 | transcript | ENST00000235329.10 | protein_coding | 8/18 | chr1 | 11999810 | ||||||
chr1:11999832
|
C | T | 1 | a0001c0001t0003g0218 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.816+737C>T | MFN2 | ENSG00000116688.18 | transcript | ENST00000235329.10 | protein_coding | 8/18 | chr1 | 11999832 | ||||||
chr1:11999883
|
A | G | 1 | a0001c0001t0002g0102 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.816+788A>G | MFN2 | ENSG00000116688.18 | transcript | ENST00000235329.10 | protein_coding | 8/18 | chr1 | 11999883 | ||||||
chr1:11999912
|
G | T | 2 | a0001c0001t0002g0021a0001c0001t0002g0105 | 3 | NA18945.hp2 NA18959.hp1 NA19063.hp2 |
intron_variant | MODIFIER | c.816+817G>T | MFN2 | ENSG00000116688.18 | transcript | ENST00000235329.10 | protein_coding | 8/18 | chr1 | 11999912 | ||||||
chr1:12000098
|
C | CA | 219 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0009others(216): Show | 254 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(251): Show |
intron_variant | MODIFIER | c.816+1009dupA | MFN2 | ENSG00000116688.18 | transcript | ENST00000235329.10 | protein_coding | 8/18 | INFO_REALIGN_3_PRIME | chr1 | 12000098 | |||||
chr1:12000216
|
G | A | 1 | a0001c0001t0002g0068 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.816+1121G>A | MFN2 | ENSG00000116688.18 | transcript | ENST00000235329.10 | protein_coding | 8/18 | chr1 | 12000216 | ||||||
chr1:12000279
|
A | G | 237 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0009others(234): Show | 274 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(271): Show |
intron_variant | MODIFIER | c.817-1122A>G | MFN2 | ENSG00000116688.18 | transcript | ENST00000235329.10 | protein_coding | 8/18 | chr1 | 12000279 | ||||||
chr1:12000297
|
A | G | 7 | a0001c0003t0007g0035a0001c0003t0007g0280a0001c0003t0007g0281others(4): Show | 8 | HG01109.hp1 HG01167.hp1 HG02145.hp2 others(5): Show |
intron_variant | MODIFIER | c.817-1104A>G | MFN2 | ENSG00000116688.18 | transcript | ENST00000235329.10 | protein_coding | 8/18 | chr1 | 12000297 | ||||||
chr1:12000436
|
C | T | 2 | a0001c0003t0017g0292a0001c0003t0017g0293 | 2 | HG01109.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.817-965C>T | MFN2 | ENSG00000116688.18 | transcript | ENST00000235329.10 | protein_coding | 8/18 | chr1 | 12000436 | ||||||
chr1:12000444
|
C | T | 3 | a0001c0001t0003g0210a0001c0001t0003g0230a0001c0001t0003g0246 | 3 | HG00735.hp1 HG01516.hp2 HG01517.hp2 |
intron_variant | MODIFIER | c.817-957C>T | MFN2 | ENSG00000116688.18 | transcript | ENST00000235329.10 | protein_coding | 8/18 | chr1 | 12000444 | ||||||
chr1:12000466
|
G | A | 4 | a0001c0001t0012g0036a0001c0001t0012g0302a0001c0001t0013g0032others(1): Show | 6 | HG02109.hp2 HG02145.hp1 HG02970.hp2 others(3): Show |
intron_variant | MODIFIER | c.817-935G>A | MFN2 | ENSG00000116688.18 | transcript | ENST00000235329.10 | protein_coding | 8/18 | chr1 | 12000466 | ||||||
chr1:12000508
|
T | C | 183 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0009others(180): Show | 215 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(212): Show |
intron_variant | MODIFIER | c.817-893T>C | MFN2 | ENSG00000116688.18 | transcript | ENST00000235329.10 | protein_coding | 8/18 | chr1 | 12000508 | ||||||
chr1:12000508
|
T | G | 1 | a0001c0001t0003g0239 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.817-893T>G | MFN2 | ENSG00000116688.18 | transcript | ENST00000235329.10 | protein_coding | 8/18 | chr1 | 12000508 | ||||||
chr1:12000547
|
A | G | 1 | a0001c0001t0001g0074 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.817-854A>G | MFN2 | ENSG00000116688.18 | transcript | ENST00000235329.10 | protein_coding | 8/18 | chr1 | 12000547 | ||||||
chr1:12000705
|
C | T | 1 | a0001c0001t0002g0090 | 1 | NA18980.hp2 | intron_variant | MODIFIER | c.817-696C>T | MFN2 | ENSG00000116688.18 | transcript | ENST00000235329.10 | protein_coding | 8/18 | chr1 | 12000705 | ||||||
chr1:12000812
|
A | G | 35 | a0001c0002t0005g0033a0001c0002t0005g0055a0001c0002t0005g0089others(32): Show | 38 | HG00408.hp1 HG00733.hp2 HG01109.hp1 others(35): Show |
intron_variant | MODIFIER | c.817-589A>G | MFN2 | ENSG00000116688.18 | transcript | ENST00000235329.10 | protein_coding | 8/18 | chr1 | 12000812 | ||||||
chr1:12000841
|
C | T | 1 | a0001c0001t0002g0070 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.817-560C>T | MFN2 | ENSG00000116688.18 | transcript | ENST00000235329.10 | protein_coding | 8/18 | chr1 | 12000841 | ||||||
chr1:12001035
|
T | C | 1 | a0001c0005t0004g0294 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.817-366T>C | MFN2 | ENSG00000116688.18 | transcript | ENST00000235329.10 | protein_coding | 8/18 | chr1 | 12001035 | ||||||
chr1:12001573
|
G | A | 4 | a0001c0001t0004g0048a0001c0001t0004g0129a0001c0001t0004g0175others(1): Show | 4 | HG01884.hp2 HG02896.hp1 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.970+19G>A | MFN2 | ENSG00000116688.18 | transcript | ENST00000235329.10 | protein_coding | 9/18 | chr1 | 12001573 | ||||||
chr1:12001605
|
G | A | 2 | a0001c0001t0002g0096a0001c0001t0002g0097 | 2 | HG01256.hp1 HG01258.hp1 |
intron_variant | MODIFIER | c.970+51G>A | MFN2 | ENSG00000116688.18 | transcript | ENST00000235329.10 | protein_coding | 9/18 | chr1 | 12001605 | ||||||
chr1:12001941
|
C | G | 6 | a0001c0001t0004g0296a0001c0001t0004g0297a0001c0001t0004g0298others(3): Show | 6 | HG02630.hp2 HG02895.hp2 HG03195.hp2 others(3): Show |
intron_variant | MODIFIER | c.1039-41C>G | MFN2 | ENSG00000116688.18 | transcript | ENST00000235329.10 | protein_coding | 10/18 | chr1 | 12001941 | ||||||
chr1:12001960
|
T | C | 22 | a0001c0001t0001g0074a0001c0002t0005g0033a0001c0002t0005g0055others(19): Show | 23 | HG00408.hp1 HG00733.hp2 HG01192.hp1 others(20): Show |
intron_variant | MODIFIER | c.1039-22T>C | MFN2 | ENSG00000116688.18 | transcript | ENST00000235329.10 | protein_coding | 10/18 | chr1 | 12001960 | ||||||
chr1:12001963
|
G | A | 18 | a0001c0001t0001g0173a0001c0001t0004g0016a0001c0001t0004g0048others(15): Show | 20 | HG01884.hp2 HG02280.hp2 HG02572.hp2 others(17): Show |
intron_variant | MODIFIER | c.1039-19G>A | MFN2 | ENSG00000116688.18 | transcript | ENST00000235329.10 | protein_coding | 10/18 | chr1 | 12001963 | ||||||
chr1:12002122
|
A | G | 1 | a0001c0005t0004g0122 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1160+19A>G | MFN2 | ENSG00000116688.18 | transcript | ENST00000235329.10 | protein_coding | 11/18 | chr1 | 12002122 | ||||||
chr1:12002148
|
A | G | 219 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0009others(216): Show | 254 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(251): Show |
intron_variant | MODIFIER | c.1160+45A>G | MFN2 | ENSG00000116688.18 | transcript | ENST00000235329.10 | protein_coding | 11/18 | chr1 | 12002148 | ||||||
chr1:12002304
|
C | G | 184 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0009others(181): Show | 216 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(213): Show |
intron_variant | MODIFIER | c.1160+201C>G | MFN2 | ENSG00000116688.18 | transcript | ENST00000235329.10 | protein_coding | 11/18 | chr1 | 12002304 | ||||||
chr1:12002344
|
T | C | 1 | a0001c0003t0007g0283 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.1160+241T>C | MFN2 | ENSG00000116688.18 | transcript | ENST00000235329.10 | protein_coding | 11/18 | chr1 | 12002344 | ||||||
chr1:12002418
|
G | A | 1 | a0001c0001t0001g0138 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.1160+315G>A | MFN2 | ENSG00000116688.18 | transcript | ENST00000235329.10 | protein_coding | 11/18 | chr1 | 12002418 | ||||||
chr1:12002450
|
T | G | 180 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0009others(177): Show | 210 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(207): Show |
intron_variant | MODIFIER | c.1160+347T>G | MFN2 | ENSG00000116688.18 | transcript | ENST00000235329.10 | protein_coding | 11/18 | chr1 | 12002450 | ||||||
chr1:12002919
|
G | A | 1 | a0001c0002t0005g0055 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.1160+816G>A | MFN2 | ENSG00000116688.18 | transcript | ENST00000235329.10 | protein_coding | 11/18 | chr1 | 12002919 | ||||||
chr1:12002975
|
C | T | 1 | a0001c0001t0026g0272 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.1160+872C>T | MFN2 | ENSG00000116688.18 | transcript | ENST00000235329.10 | protein_coding | 11/18 | chr1 | 12002975 | ||||||
chr1:12003083
|
AT | A | 33 | a0001c0002t0005g0033a0001c0002t0005g0055a0001c0002t0005g0089others(30): Show | 36 | HG00408.hp1 HG00733.hp2 HG01167.hp1 others(33): Show |
intron_variant | MODIFIER | c.1161-899delT | MFN2 | ENSG00000116688.18 | transcript | ENST00000235329.10 | protein_coding | 11/18 | INFO_REALIGN_3_PRIME | chr1 | 12003083 | |||||
chr1:12003141
|
G | A | 12 | a0001c0001t0001g0173a0001c0001t0004g0016a0001c0001t0004g0048others(9): Show | 14 | HG01884.hp2 HG02280.hp2 HG02572.hp2 others(11): Show |
intron_variant | MODIFIER | c.1161-851G>A | MFN2 | ENSG00000116688.18 | transcript | ENST00000235329.10 | protein_coding | 11/18 | chr1 | 12003141 | ||||||
chr1:12003174
|
TC | T | 28 | a0001c0002t0005g0033a0001c0002t0005g0055a0001c0002t0005g0089others(25): Show | 30 | HG00408.hp1 HG00733.hp2 HG01192.hp1 others(27): Show |
intron_variant | MODIFIER | c.1161-816delC | MFN2 | ENSG00000116688.18 | transcript | ENST00000235329.10 | protein_coding | 11/18 | INFO_REALIGN_3_PRIME | chr1 | 12003174 | |||||
chr1:12003216
|
C | T | 4 | a0001c0001t0012g0036a0001c0001t0012g0302a0001c0001t0013g0032others(1): Show | 6 | HG02109.hp2 HG02145.hp1 HG02970.hp2 others(3): Show |
intron_variant | MODIFIER | c.1161-776C>T | MFN2 | ENSG00000116688.18 | transcript | ENST00000235329.10 | protein_coding | 11/18 | chr1 | 12003216 | ||||||
chr1:12003237
|
A | AT | 33 | a0001c0002t0005g0033a0001c0002t0005g0055a0001c0002t0005g0089others(30): Show | 36 | HG00408.hp1 HG00733.hp2 HG01167.hp1 others(33): Show |
intron_variant | MODIFIER | c.1161-754dupT | MFN2 | ENSG00000116688.18 | transcript | ENST00000235329.10 | protein_coding | 11/18 | INFO_REALIGN_3_PRIME | chr1 | 12003237 | |||||
chr1:12003250
|
C | T | 1 | a0001c0001t0002g0061 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.1161-742C>T | MFN2 | ENSG00000116688.18 | transcript | ENST00000235329.10 | protein_coding | 11/18 | chr1 | 12003250 | ||||||
chr1:12003533
|
G | A | 4 | a0001c0001t0012g0036a0001c0001t0012g0302a0001c0001t0013g0032others(1): Show | 6 | HG02109.hp2 HG02145.hp1 HG02970.hp2 others(3): Show |
intron_variant | MODIFIER | c.1161-459G>A | MFN2 | ENSG00000116688.18 | transcript | ENST00000235329.10 | protein_coding | 11/18 | chr1 | 12003533 | ||||||
chr1:12003556
|
C | T | 1 | a0001c0001t0002g0098 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.1161-436C>T | MFN2 | ENSG00000116688.18 | transcript | ENST00000235329.10 | protein_coding | 11/18 | chr1 | 12003556 | ||||||
chr1:12003589
|
A | G | 2 | a0001c0001t0001g0054a0001c0001t0004g0284 | 2 | HG02615.hp1 HG02965.hp1 |
intron_variant | MODIFIER | c.1161-403A>G | MFN2 | ENSG00000116688.18 | transcript | ENST00000235329.10 | protein_coding | 11/18 | chr1 | 12003589 | ||||||
chr1:12003664
|
C | CA | 45 | a0001c0001t0001g0121a0001c0001t0001g0145a0001c0001t0001g0166others(42): Show | 48 | HG00408.hp1 HG00733.hp2 HG01109.hp1 others(45): Show |
intron_variant | MODIFIER | c.1161-312dupA | MFN2 | ENSG00000116688.18 | transcript | ENST00000235329.10 | protein_coding | 11/18 | INFO_REALIGN_3_PRIME | chr1 | 12003664 | |||||
chr1:12003664
|
C | CAA | 7 | a0001c0004t0004g0034a0001c0004t0004g0265a0001c0004t0004g0267others(4): Show | 8 | HG02083.hp2 HG04228.hp2 NA18952.hp2 others(5): Show |
intron_variant | MODIFIER | c.1161-313_1161-312d others(4): Show |
MFN2 | ENSG00000116688.18 | transcript | ENST00000235329.10 | protein_coding | 11/18 | INFO_REALIGN_3_PRIME | chr1 | 12003664 | |||||
chr1:12003664
|
CA | C | 5 | a0001c0001t0002g0097a0001c0001t0012g0036a0001c0001t0012g0302others(2): Show | 7 | HG01256.hp1 HG02109.hp2 HG02145.hp1 others(4): Show |
intron_variant | MODIFIER | c.1161-312delA | MFN2 | ENSG00000116688.18 | transcript | ENST00000235329.10 | protein_coding | 11/18 | INFO_REALIGN_3_PRIME | chr1 | 12003664 | |||||
chr1:12003795
|
C | T | 1 | a0001c0001t0001g0160 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.1161-197C>T | MFN2 | ENSG00000116688.18 | transcript | ENST00000235329.10 | protein_coding | 11/18 | chr1 | 12003795 | ||||||
chr1:12003922
|
T | C | 1 | a0001c0001t0002g0079 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.1161-70T>C | MFN2 | ENSG00000116688.18 | transcript | ENST00000235329.10 | protein_coding | 11/18 | chr1 | 12003922 | ||||||
chr1:12004160
|
C | T | 1 | a0001c0001t0001g0132 | 1 | NA18951.hp1 | intron_variant | MODIFIER | c.1287+42C>T | MFN2 | ENSG00000116688.18 | transcript | ENST00000235329.10 | protein_coding | 12/18 | chr1 | 12004160 | ||||||
chr1:12004164
|
T | C | 1 | a0001c0001t0004g0194 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.1287+46T>C | MFN2 | ENSG00000116688.18 | transcript | ENST00000235329.10 | protein_coding | 12/18 | chr1 | 12004164 | ||||||
chr1:12004266
|
C | G | 7 | a0001c0004t0004g0034a0001c0004t0004g0265a0001c0004t0004g0267others(4): Show | 8 | HG02083.hp2 HG04228.hp2 NA18952.hp2 others(5): Show |
intron_variant | MODIFIER | c.1287+148C>G | MFN2 | ENSG00000116688.18 | transcript | ENST00000235329.10 | protein_coding | 12/18 | chr1 | 12004266 | ||||||
chr1:12004711
|
A | C | 3 | a0001c0001t0016g0086a0001c0001t0016g0088a0001c0001t0019g0107 | 3 | HG02698.hp1 HG03710.hp1 HG03942.hp2 |
intron_variant | MODIFIER | c.1392+98A>C | MFN2 | ENSG00000116688.18 | transcript | ENST00000235329.10 | protein_coding | 13/18 | chr1 | 12004711 | ||||||
chr1:12004760
|
G | A | 5 | a0001c0001t0001g0135a0001c0001t0001g0139a0001c0001t0001g0144others(2): Show | 5 | NA18959.hp2 NA19005.hp1 NA19009.hp1 others(2): Show |
intron_variant | MODIFIER | c.1393-65G>A | MFN2 | ENSG00000116688.18 | transcript | ENST00000235329.10 | protein_coding | 13/18 | chr1 | 12004760 | ||||||
chr1:12004769
|
G | A | 1 | a0001c0001t0001g0073 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.1393-56G>A | MFN2 | ENSG00000116688.18 | transcript | ENST00000235329.10 | protein_coding | 13/18 | chr1 | 12004769 | ||||||
chr1:12004769
|
G | C | 1 | a0001c0001t0001g0168 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.1393-56G>C | MFN2 | ENSG00000116688.18 | transcript | ENST00000235329.10 | protein_coding | 13/18 | chr1 | 12004769 | ||||||
chr1:12005113
|
A | G | 28 | a0001c0002t0005g0033a0001c0002t0005g0055a0001c0002t0005g0089others(25): Show | 30 | HG00408.hp1 HG00733.hp2 HG01192.hp1 others(27): Show |
intron_variant | MODIFIER | c.1495+186A>G | MFN2 | ENSG00000116688.18 | transcript | ENST00000235329.10 | protein_coding | 14/18 | chr1 | 12005113 | ||||||
chr1:12005163
|
C | A | 1 | a0001c0001t0006g0038 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.1495+236C>A | MFN2 | ENSG00000116688.18 | transcript | ENST00000235329.10 | protein_coding | 14/18 | chr1 | 12005163 | ||||||
chr1:12005237
|
C | T | 5 | a0001c0001t0004g0030a0001c0001t0004g0191a0001c0001t0004g0192others(2): Show | 6 | HG02451.hp2 HG02572.hp1 HG02818.hp2 others(3): Show |
intron_variant | MODIFIER | c.1495+310C>T | MFN2 | ENSG00000116688.18 | transcript | ENST00000235329.10 | protein_coding | 14/18 | chr1 | 12005237 | ||||||
chr1:12005565
|
C | T | 1 | a0001c0001t0002g0289 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.1496-146C>T | MFN2 | ENSG00000116688.18 | transcript | ENST00000235329.10 | protein_coding | 14/18 | chr1 | 12005565 | ||||||
chr1:12005677
|
T | C | 3 | a0001c0001t0015g0050a0001c0001t0015g0051a0001c0001t0015g0053 | 3 | HG02559.hp1 HG02723.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.1496-34T>C | MFN2 | ENSG00000116688.18 | transcript | ENST00000235329.10 | protein_coding | 14/18 | chr1 | 12005677 | ||||||
chr1:12005968
|
G | C | 4 | a0001c0001t0001g0169a0001c0001t0001g0170a0001c0001t0001g0171others(1): Show | 4 | HG01243.hp2 HG02615.hp2 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.1716+37G>C | MFN2 | ENSG00000116688.18 | transcript | ENST00000235329.10 | protein_coding | 15/18 | chr1 | 12005968 | ||||||
chr1:12006021
|
C | CCT | 18 | a0001c0001t0001g0173a0001c0001t0004g0016a0001c0001t0004g0048others(15): Show | 20 | HG01884.hp2 HG02280.hp2 HG02572.hp2 others(17): Show |
intron_variant | MODIFIER | c.1716+91_1716+92dup others(2): Show |
MFN2 | ENSG00000116688.18 | transcript | ENST00000235329.10 | protein_coding | 15/18 | INFO_REALIGN_3_PRIME | chr1 | 12006021 | |||||
chr1:12006056
|
C | T | 18 | a0001c0001t0001g0173a0001c0001t0004g0016a0001c0001t0004g0048others(15): Show | 20 | HG01884.hp2 HG02280.hp2 HG02572.hp2 others(17): Show |
intron_variant | MODIFIER | c.1716+125C>T | MFN2 | ENSG00000116688.18 | transcript | ENST00000235329.10 | protein_coding | 15/18 | chr1 | 12006056 | ||||||
chr1:12006161
|
T | TA | 191 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0009others(188): Show | 224 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(221): Show |
intron_variant | MODIFIER | c.1716+233dupA | MFN2 | ENSG00000116688.18 | transcript | ENST00000235329.10 | protein_coding | 15/18 | INFO_REALIGN_3_PRIME | chr1 | 12006161 | |||||
chr1:12006215
|
T | TACGACTA others(315): Show |
1 | a0001c0008t0004g0268 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.1716+295_1716+296i others(324): Show |
MFN2 | ENSG00000116688.18 | transcript | ENST00000235329.10 | protein_coding | 15/18 | INFO_REALIGN_3_PRIME | chr1 | 12006215 | |||||
chr1:12006215
|
T | TACGACTA others(316): Show |
1 | a0001c0004t0004g0269 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.1716+295_1716+296i others(325): Show |
MFN2 | ENSG00000116688.18 | transcript | ENST00000235329.10 | protein_coding | 15/18 | INFO_REALIGN_3_PRIME | chr1 | 12006215 | |||||
chr1:12006215
|
T | TACGACTA others(317): Show |
4 | a0001c0004t0004g0034a0001c0004t0004g0267a0001c0004t0004g0271others(1): Show | 5 | HG02083.hp2 HG04228.hp2 NA18952.hp2 others(2): Show |
intron_variant | MODIFIER | c.1716+295_1716+296i others(326): Show |
MFN2 | ENSG00000116688.18 | transcript | ENST00000235329.10 | protein_coding | 15/18 | INFO_REALIGN_3_PRIME | chr1 | 12006215 | |||||
chr1:12006215
|
T | TACGACTA others(318): Show |
1 | a0001c0004t0004g0265 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.1716+295_1716+296i others(327): Show |
MFN2 | ENSG00000116688.18 | transcript | ENST00000235329.10 | protein_coding | 15/18 | INFO_REALIGN_3_PRIME | chr1 | 12006215 | |||||
chr1:12006267
|
A | G | 28 | a0001c0002t0005g0033a0001c0002t0005g0055a0001c0002t0005g0089others(25): Show | 30 | HG00408.hp1 HG00733.hp2 HG01192.hp1 others(27): Show |
intron_variant | MODIFIER | c.1717-271A>G | MFN2 | ENSG00000116688.18 | transcript | ENST00000235329.10 | protein_coding | 15/18 | chr1 | 12006267 | ||||||
chr1:12006354
|
C | T | 1 | a0001c0001t0004g0194 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.1717-184C>T | MFN2 | ENSG00000116688.18 | transcript | ENST00000235329.10 | protein_coding | 15/18 | chr1 | 12006354 | ||||||
chr1:12006361
|
T | C | 13 | a0001c0001t0004g0047a0001c0001t0006g0037a0001c0001t0006g0038others(10): Show | 13 | HG01192.hp2 HG01891.hp2 HG02280.hp1 others(10): Show |
intron_variant | MODIFIER | c.1717-177T>C | MFN2 | ENSG00000116688.18 | transcript | ENST00000235329.10 | protein_coding | 15/18 | chr1 | 12006361 | ||||||
chr1:12006504
|
G | A | 1 | a0001c0001t0027g0052 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.1717-34G>A | MFN2 | ENSG00000116688.18 | transcript | ENST00000235329.10 | protein_coding | 15/18 | chr1 | 12006504 | ||||||
chr1:12006756
|
T | C | 22 | a0001c0001t0003g0229a0001c0001t0003g0236a0001c0002t0005g0033others(19): Show | 23 | HG00408.hp1 HG00733.hp2 HG01192.hp1 others(20): Show |
intron_variant | MODIFIER | c.1872+63T>C | MFN2 | ENSG00000116688.18 | transcript | ENST00000235329.10 | protein_coding | 16/18 | chr1 | 12006756 | ||||||
chr1:12006838
|
C | T | 1 | a0001c0001t0001g0136 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.1872+145C>T | MFN2 | ENSG00000116688.18 | transcript | ENST00000235329.10 | protein_coding | 16/18 | chr1 | 12006838 | ||||||
chr1:12006899
|
C | G | 7 | a0001c0003t0007g0035a0001c0003t0007g0280a0001c0003t0007g0281others(4): Show | 8 | HG01109.hp1 HG01167.hp1 HG02145.hp2 others(5): Show |
intron_variant | MODIFIER | c.1873-154C>G | MFN2 | ENSG00000116688.18 | transcript | ENST00000235329.10 | protein_coding | 16/18 | chr1 | 12006899 | ||||||
chr1:12006987
|
T | G | 173 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0009others(170): Show | 203 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(200): Show |
intron_variant | MODIFIER | c.1873-66T>G | MFN2 | ENSG00000116688.18 | transcript | ENST00000235329.10 | protein_coding | 16/18 | chr1 | 12006987 | ||||||
chr1:12007014
|
C | T | 1 | a0001c0001t0003g0199 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.1873-39C>T | MFN2 | ENSG00000116688.18 | transcript | ENST00000235329.10 | protein_coding | 16/18 | chr1 | 12007014 | ||||||
chr1:12007279
|
G | C | 4 | a0001c0001t0012g0036a0001c0001t0012g0302a0001c0001t0013g0032others(1): Show | 6 | HG02109.hp2 HG02145.hp1 HG02970.hp2 others(3): Show |
intron_variant | MODIFIER | c.2069+30G>C | MFN2 | ENSG00000116688.18 | transcript | ENST00000235329.10 | protein_coding | 17/18 | chr1 | 12007279 | ||||||
chr1:12007331
|
C | T | 28 | a0001c0002t0005g0033a0001c0002t0005g0055a0001c0002t0005g0089others(25): Show | 30 | HG00408.hp1 HG00733.hp2 HG01192.hp1 others(27): Show |
intron_variant | MODIFIER | c.2069+82C>T | MFN2 | ENSG00000116688.18 | transcript | ENST00000235329.10 | protein_coding | 17/18 | chr1 | 12007331 | ||||||
chr1:12007441
|
C | T | 1 | a0001c0001t0026g0272 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.2069+192C>T | MFN2 | ENSG00000116688.18 | transcript | ENST00000235329.10 | protein_coding | 17/18 | chr1 | 12007441 | ||||||
chr1:12007448
|
G | T | 7 | a0001c0001t0002g0006a0001c0001t0002g0017a0001c0001t0002g0064others(4): Show | 11 | HG01099.hp2 HG01123.hp2 HG01346.hp1 others(8): Show |
intron_variant | MODIFIER | c.2069+199G>T | MFN2 | ENSG00000116688.18 | transcript | ENST00000235329.10 | protein_coding | 17/18 | chr1 | 12007448 | ||||||
chr1:12007652
|
T | G | 28 | a0001c0002t0005g0033a0001c0002t0005g0055a0001c0002t0005g0089others(25): Show | 30 | HG00408.hp1 HG00733.hp2 HG01192.hp1 others(27): Show |
intron_variant | MODIFIER | c.2069+403T>G | MFN2 | ENSG00000116688.18 | transcript | ENST00000235329.10 | protein_coding | 17/18 | chr1 | 12007652 | ||||||
chr1:12007669
|
T | G | 1 | a0001c0002t0005g0256 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.2069+420T>G | MFN2 | ENSG00000116688.18 | transcript | ENST00000235329.10 | protein_coding | 17/18 | chr1 | 12007669 | ||||||
chr1:12007749
|
A | T | 6 | a0001c0001t0004g0296a0001c0001t0004g0297a0001c0001t0004g0298others(3): Show | 6 | HG02630.hp2 HG02895.hp2 HG03195.hp2 others(3): Show |
intron_variant | MODIFIER | c.2069+500A>T | MFN2 | ENSG00000116688.18 | transcript | ENST00000235329.10 | protein_coding | 17/18 | chr1 | 12007749 | ||||||
chr1:12007775
|
T | C | 10 | a0001c0001t0006g0037a0001c0001t0006g0038a0001c0001t0006g0040others(7): Show | 10 | HG01192.hp2 HG02280.hp1 HG02630.hp1 others(7): Show |
intron_variant | MODIFIER | c.2069+526T>C | MFN2 | ENSG00000116688.18 | transcript | ENST00000235329.10 | protein_coding | 17/18 | chr1 | 12007775 | ||||||
chr1:12007778
|
T | C | 4 | a0001c0001t0012g0036a0001c0001t0012g0302a0001c0001t0013g0032others(1): Show | 6 | HG02109.hp2 HG02145.hp1 HG02970.hp2 others(3): Show |
intron_variant | MODIFIER | c.2069+529T>C | MFN2 | ENSG00000116688.18 | transcript | ENST00000235329.10 | protein_coding | 17/18 | chr1 | 12007778 | ||||||
chr1:12007837
|
A | G | 184 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0009others(181): Show | 216 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(213): Show |
intron_variant | MODIFIER | c.2069+588A>G | MFN2 | ENSG00000116688.18 | transcript | ENST00000235329.10 | protein_coding | 17/18 | chr1 | 12007837 | ||||||
chr1:12008081
|
C | G | 3 | a0001c0001t0015g0050a0001c0001t0015g0051a0001c0001t0015g0053 | 3 | HG02559.hp1 HG02723.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.2069+832C>G | MFN2 | ENSG00000116688.18 | transcript | ENST00000235329.10 | protein_coding | 17/18 | chr1 | 12008081 | ||||||
chr1:12008185
|
T | C | 1 | a0001c0001t0001g0225 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.2069+936T>C | MFN2 | ENSG00000116688.18 | transcript | ENST00000235329.10 | protein_coding | 17/18 | chr1 | 12008185 | ||||||
chr1:12008225
|
G | A | 7 | a0001c0004t0004g0034a0001c0004t0004g0265a0001c0004t0004g0267others(4): Show | 8 | HG02083.hp2 HG04228.hp2 NA18952.hp2 others(5): Show |
intron_variant | MODIFIER | c.2069+976G>A | MFN2 | ENSG00000116688.18 | transcript | ENST00000235329.10 | protein_coding | 17/18 | chr1 | 12008225 | ||||||
chr1:12008230
|
C | T | 3 | a0001c0005t0004g0122a0001c0005t0004g0294a0001c0005t0004g0295 | 3 | HG02895.hp2 HG03195.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.2069+981C>T | MFN2 | ENSG00000116688.18 | transcript | ENST00000235329.10 | protein_coding | 17/18 | chr1 | 12008230 | ||||||
chr1:12008322
|
T | C | 35 | a0001c0002t0005g0033a0001c0002t0005g0055a0001c0002t0005g0089others(32): Show | 38 | HG00408.hp1 HG00733.hp2 HG01109.hp1 others(35): Show |
intron_variant | MODIFIER | c.2069+1073T>C | MFN2 | ENSG00000116688.18 | transcript | ENST00000235329.10 | protein_coding | 17/18 | chr1 | 12008322 | ||||||
chr1:12008326
|
T | C | 1 | a0001c0001t0015g0050 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.2069+1077T>C | MFN2 | ENSG00000116688.18 | transcript | ENST00000235329.10 | protein_coding | 17/18 | chr1 | 12008326 | ||||||
chr1:12008328
|
G | A | 2 | a0001c0003t0017g0292a0001c0003t0017g0293 | 2 | HG01109.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.2069+1079G>A | MFN2 | ENSG00000116688.18 | transcript | ENST00000235329.10 | protein_coding | 17/18 | chr1 | 12008328 | ||||||
chr1:12008350
|
C | T | 3 | a0001c0001t0003g0210a0001c0001t0003g0230a0001c0001t0003g0246 | 3 | HG00735.hp1 HG01516.hp2 HG01517.hp2 |
intron_variant | MODIFIER | c.2069+1101C>T | MFN2 | ENSG00000116688.18 | transcript | ENST00000235329.10 | protein_coding | 17/18 | chr1 | 12008350 | ||||||
chr1:12008351
|
G | A | 21 | a0001c0002t0005g0033a0001c0002t0005g0055a0001c0002t0005g0089others(18): Show | 22 | HG00408.hp1 HG00733.hp2 HG01192.hp1 others(19): Show |
intron_variant | MODIFIER | c.2069+1102G>A | MFN2 | ENSG00000116688.18 | transcript | ENST00000235329.10 | protein_coding | 17/18 | chr1 | 12008351 | ||||||
chr1:12008367
|
G | A | 3 | a0001c0001t0001g0028a0001c0001t0001g0141a0001c0001t0001g0149 | 4 | HG01069.hp1 HG01071.hp1 HG01515.hp1 others(1): Show |
intron_variant | MODIFIER | c.2069+1118G>A | MFN2 | ENSG00000116688.18 | transcript | ENST00000235329.10 | protein_coding | 17/18 | chr1 | 12008367 | ||||||
chr1:12008394
|
G | A | 180 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0009others(177): Show | 210 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(207): Show |
intron_variant | MODIFIER | c.2069+1145G>A | MFN2 | ENSG00000116688.18 | transcript | ENST00000235329.10 | protein_coding | 17/18 | chr1 | 12008394 | ||||||
chr1:12008423
|
AC | A | 207 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0009others(204): Show | 242 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(239): Show |
intron_variant | MODIFIER | c.2070-1161delC | MFN2 | ENSG00000116688.18 | transcript | ENST00000235329.10 | protein_coding | 17/18 | INFO_REALIGN_3_PRIME | chr1 | 12008423 | |||||
chr1:12008424
|
CCCCCCCC others(41): Show |
C | 12 | a0001c0001t0004g0047a0001c0001t0006g0037a0001c0001t0006g0038others(9): Show | 12 | HG01192.hp2 HG01891.hp2 HG02280.hp1 others(9): Show |
intron_variant | MODIFIER | c.2070-1161_2070-111 others(52): Show |
MFN2 | ENSG00000116688.18 | transcript | ENST00000235329.10 | protein_coding | 17/18 | INFO_REALIGN_3_PRIME | chr1 | 12008424 | |||||
chr1:12008428
|
C | T | 3 | a0001c0001t0003g0220a0001c0001t0003g0223a0001c0001t0003g0224 | 3 | NA18970.hp2 NA19011.hp1 NA19056.hp1 |
intron_variant | MODIFIER | c.2070-1164C>T | MFN2 | ENSG00000116688.18 | transcript | ENST00000235329.10 | protein_coding | 17/18 | chr1 | 12008428 | ||||||
chr1:12008446
|
C | T | 1 | a0001c0001t0003g0234 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.2070-1146C>T | MFN2 | ENSG00000116688.18 | transcript | ENST00000235329.10 | protein_coding | 17/18 | chr1 | 12008446 | ||||||
chr1:12008454
|
C | T | 172 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0009others(169): Show | 204 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(201): Show |
intron_variant | MODIFIER | c.2070-1138C>T | MFN2 | ENSG00000116688.18 | transcript | ENST00000235329.10 | protein_coding | 17/18 | chr1 | 12008454 | ||||||
chr1:12008463
|
C | T | 2 | a0001c0001t0001g0114a0001c0001t0001g0287 | 2 | HG02257.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.2070-1129C>T | MFN2 | ENSG00000116688.18 | transcript | ENST00000235329.10 | protein_coding | 17/18 | chr1 | 12008463 | ||||||
chr1:12008468
|
A | G | 225 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0009others(222): Show | 262 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(259): Show |
intron_variant | MODIFIER | c.2070-1124A>G | MFN2 | ENSG00000116688.18 | transcript | ENST00000235329.10 | protein_coding | 17/18 | chr1 | 12008468 | ||||||
chr1:12008489
|
C | T | 168 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0009others(165): Show | 198 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(195): Show |
intron_variant | MODIFIER | c.2070-1103C>T | MFN2 | ENSG00000116688.18 | transcript | ENST00000235329.10 | protein_coding | 17/18 | chr1 | 12008489 | ||||||
chr1:12008532
|
C | T | 180 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0009others(177): Show | 210 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(207): Show |
intron_variant | MODIFIER | c.2070-1060C>T | MFN2 | ENSG00000116688.18 | transcript | ENST00000235329.10 | protein_coding | 17/18 | chr1 | 12008532 | ||||||
chr1:12008544
|
G | A | 4 | a0001c0001t0012g0036a0001c0001t0012g0302a0001c0001t0013g0032others(1): Show | 6 | HG02109.hp2 HG02145.hp1 HG02970.hp2 others(3): Show |
intron_variant | MODIFIER | c.2070-1048G>A | MFN2 | ENSG00000116688.18 | transcript | ENST00000235329.10 | protein_coding | 17/18 | chr1 | 12008544 | ||||||
chr1:12008599
|
C | T | 59 | a0001c0001t0001g0237a0001c0001t0003g0003a0001c0001t0003g0031others(56): Show | 65 | HG00280.hp2 HG00408.hp2 HG00423.hp1 others(62): Show |
intron_variant | MODIFIER | c.2070-993C>T | MFN2 | ENSG00000116688.18 | transcript | ENST00000235329.10 | protein_coding | 17/18 | chr1 | 12008599 | ||||||
chr1:12008603
|
T | C | 237 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0009others(234): Show | 274 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(271): Show |
intron_variant | MODIFIER | c.2070-989T>C | MFN2 | ENSG00000116688.18 | transcript | ENST00000235329.10 | protein_coding | 17/18 | chr1 | 12008603 | ||||||
chr1:12008607
|
C | T | 7 | a0001c0004t0004g0034a0001c0004t0004g0265a0001c0004t0004g0267others(4): Show | 8 | HG02083.hp2 HG04228.hp2 NA18952.hp2 others(5): Show |
intron_variant | MODIFIER | c.2070-985C>T | MFN2 | ENSG00000116688.18 | transcript | ENST00000235329.10 | protein_coding | 17/18 | chr1 | 12008607 | ||||||
chr1:12008609
|
G | A | 1 | a0001c0001t0004g0047 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.2070-983G>A | MFN2 | ENSG00000116688.18 | transcript | ENST00000235329.10 | protein_coding | 17/18 | chr1 | 12008609 | ||||||
chr1:12008635
|
TCA | T | 5 | a0001c0001t0004g0030a0001c0001t0004g0191a0001c0001t0004g0192others(2): Show | 6 | HG02451.hp2 HG02572.hp1 HG02818.hp2 others(3): Show |
intron_variant | MODIFIER | c.2070-954_2070-953d others(4): Show |
MFN2 | ENSG00000116688.18 | transcript | ENST00000235329.10 | protein_coding | 17/18 | INFO_REALIGN_3_PRIME | chr1 | 12008635 | |||||
chr1:12008684
|
T | C | 7 | a0001c0003t0007g0035a0001c0003t0007g0280a0001c0003t0007g0281others(4): Show | 8 | HG01109.hp1 HG01167.hp1 HG02145.hp2 others(5): Show |
intron_variant | MODIFIER | c.2070-908T>C | MFN2 | ENSG00000116688.18 | transcript | ENST00000235329.10 | protein_coding | 17/18 | chr1 | 12008684 | ||||||
chr1:12008761
|
C | T | 1 | a0001c0001t0006g0041 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.2070-831C>T | MFN2 | ENSG00000116688.18 | transcript | ENST00000235329.10 | protein_coding | 17/18 | chr1 | 12008761 | ||||||
chr1:12008769
|
G | A | 28 | a0001c0002t0005g0033a0001c0002t0005g0055a0001c0002t0005g0089others(25): Show | 30 | HG00408.hp1 HG00733.hp2 HG01192.hp1 others(27): Show |
intron_variant | MODIFIER | c.2070-823G>A | MFN2 | ENSG00000116688.18 | transcript | ENST00000235329.10 | protein_coding | 17/18 | chr1 | 12008769 | ||||||
chr1:12008795
|
T | C | 35 | a0001c0002t0005g0033a0001c0002t0005g0055a0001c0002t0005g0089others(32): Show | 38 | HG00408.hp1 HG00733.hp2 HG01109.hp1 others(35): Show |
intron_variant | MODIFIER | c.2070-797T>C | MFN2 | ENSG00000116688.18 | transcript | ENST00000235329.10 | protein_coding | 17/18 | chr1 | 12008795 | ||||||
chr1:12008798
|
G | T | 1 | a0001c0001t0001g0225 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.2070-794G>T | MFN2 | ENSG00000116688.18 | transcript | ENST00000235329.10 | protein_coding | 17/18 | chr1 | 12008798 | ||||||
chr1:12008800
|
C | CG | 3 | a0001c0001t0002g0022a0001c0001t0003g0250a0001c0001t0009g0140 | 4 | NA18969.hp2 NA18981.hp2 NA19012.hp2 others(1): Show |
intron_variant | MODIFIER | c.2070-788dupG | MFN2 | ENSG00000116688.18 | transcript | ENST00000235329.10 | protein_coding | 17/18 | INFO_REALIGN_3_PRIME | chr1 | 12008800 | |||||
chr1:12008813
|
G | A | 1 | a0001c0001t0001g0125 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.2070-779G>A | MFN2 | ENSG00000116688.18 | transcript | ENST00000235329.10 | protein_coding | 17/18 | chr1 | 12008813 | ||||||
chr1:12008884
|
T | C | 244 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0009others(241): Show | 282 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(279): Show |
intron_variant | MODIFIER | c.2070-708T>C | MFN2 | ENSG00000116688.18 | transcript | ENST00000235329.10 | protein_coding | 17/18 | chr1 | 12008884 | ||||||
chr1:12008885
|
G | A | 8 | a0001c0001t0001g0072a0001c0004t0004g0034a0001c0004t0004g0265others(5): Show | 9 | HG00639.hp1 HG02083.hp2 HG04228.hp2 others(6): Show |
intron_variant | MODIFIER | c.2070-707G>A | MFN2 | ENSG00000116688.18 | transcript | ENST00000235329.10 | protein_coding | 17/18 | chr1 | 12008885 | ||||||
chr1:12008928
|
G | A | 1 | a0001c0001t0003g0248 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.2070-664G>A | MFN2 | ENSG00000116688.18 | transcript | ENST00000235329.10 | protein_coding | 17/18 | chr1 | 12008928 | ||||||
chr1:12008955
|
C | G | 1 | a0001c0001t0001g0148 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.2070-637C>G | MFN2 | ENSG00000116688.18 | transcript | ENST00000235329.10 | protein_coding | 17/18 | chr1 | 12008955 | ||||||
chr1:12008964
|
G | A | 28 | a0001c0002t0005g0033a0001c0002t0005g0055a0001c0002t0005g0089others(25): Show | 30 | HG00408.hp1 HG00733.hp2 HG01192.hp1 others(27): Show |
intron_variant | MODIFIER | c.2070-628G>A | MFN2 | ENSG00000116688.18 | transcript | ENST00000235329.10 | protein_coding | 17/18 | chr1 | 12008964 | ||||||
chr1:12009004
|
C | T | 3 | a0001c0005t0004g0122a0001c0005t0004g0294a0001c0005t0004g0295 | 3 | HG02895.hp2 HG03195.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.2070-588C>T | MFN2 | ENSG00000116688.18 | transcript | ENST00000235329.10 | protein_coding | 17/18 | chr1 | 12009004 | ||||||
chr1:12009068
|
C | T | 1 | a0001c0001t0001g0158 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.2070-524C>T | MFN2 | ENSG00000116688.18 | transcript | ENST00000235329.10 | protein_coding | 17/18 | chr1 | 12009068 | ||||||
chr1:12009073
|
G | A | 28 | a0001c0002t0005g0033a0001c0002t0005g0055a0001c0002t0005g0089others(25): Show | 30 | HG00408.hp1 HG00733.hp2 HG01192.hp1 others(27): Show |
intron_variant | MODIFIER | c.2070-519G>A | MFN2 | ENSG00000116688.18 | transcript | ENST00000235329.10 | protein_coding | 17/18 | chr1 | 12009073 | ||||||
chr1:12009082
|
C | T | 1 | a0001c0001t0025g0301 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.2070-510C>T | MFN2 | ENSG00000116688.18 | transcript | ENST00000235329.10 | protein_coding | 17/18 | chr1 | 12009082 | ||||||
chr1:12009187
|
G | A | 1 | a0001c0001t0004g0195 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.2070-405G>A | MFN2 | ENSG00000116688.18 | transcript | ENST00000235329.10 | protein_coding | 17/18 | chr1 | 12009187 | ||||||
chr1:12009197
|
AGGGAGAG others(28): Show |
A | 2 | a0001c0001t0001g0147a0001c0001t0001g0152 | 2 | HG02165.hp1 NA19065.hp2 |
intron_variant | MODIFIER | c.2070-382_2070-348d others(37): Show |
MFN2 | ENSG00000116688.18 | transcript | ENST00000235329.10 | protein_coding | 17/18 | INFO_REALIGN_3_PRIME | chr1 | 12009197 | |||||
chr1:12009221
|
G | A | 1 | a0001c0001t0003g0202 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.2070-371G>A | MFN2 | ENSG00000116688.18 | transcript | ENST00000235329.10 | protein_coding | 17/18 | chr1 | 12009221 | ||||||
chr1:12009529
|
C | T | 7 | a0001c0003t0007g0035a0001c0003t0007g0280a0001c0003t0007g0281others(4): Show | 8 | HG01109.hp1 HG01167.hp1 HG02145.hp2 others(5): Show |
intron_variant | MODIFIER | c.2070-63C>T | MFN2 | ENSG00000116688.18 | transcript | ENST00000235329.10 | protein_coding | 17/18 | chr1 | 12009529 | ||||||
chr1:12009547
|
C | T | 1 | a0001c0001t0002g0094 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.2070-45C>T | MFN2 | ENSG00000116688.18 | transcript | ENST00000235329.10 | protein_coding | 17/18 | chr1 | 12009547 | ||||||
chr1:12009741
|
T | C | 35 | a0001c0002t0005g0033a0001c0002t0005g0055a0001c0002t0005g0089others(32): Show | 38 | HG00408.hp1 HG00733.hp2 HG01109.hp1 others(35): Show |
intron_variant | MODIFIER | c.2204+15T>C | MFN2 | ENSG00000116688.18 | transcript | ENST00000235329.10 | protein_coding | 18/18 | chr1 | 12009741 | ||||||
chr1:12009805
|
C | T | 1 | a0001c0001t0003g0223 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.2204+79C>T | MFN2 | ENSG00000116688.18 | transcript | ENST00000235329.10 | protein_coding | 18/18 | chr1 | 12009805 | ||||||
chr1:12009844
|
A | G | 2 | a0001c0003t0017g0292a0001c0003t0017g0293 | 2 | HG01109.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.2204+118A>G | MFN2 | ENSG00000116688.18 | transcript | ENST00000235329.10 | protein_coding | 18/18 | chr1 | 12009844 | ||||||
chr1:12010173
|
G | T | 1 | a0001c0001t0003g0246 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.2204+447G>T | MFN2 | ENSG00000116688.18 | transcript | ENST00000235329.10 | protein_coding | 18/18 | chr1 | 12010173 | ||||||
chr1:12010231
|
C | T | 3 | a0001c0005t0004g0122a0001c0005t0004g0294a0001c0005t0004g0295 | 3 | HG02895.hp2 HG03195.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.2204+505C>T | MFN2 | ENSG00000116688.18 | transcript | ENST00000235329.10 | protein_coding | 18/18 | chr1 | 12010231 | ||||||
chr1:12010235
|
G | A | 180 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0009others(177): Show | 210 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(207): Show |
intron_variant | MODIFIER | c.2204+509G>A | MFN2 | ENSG00000116688.18 | transcript | ENST00000235329.10 | protein_coding | 18/18 | chr1 | 12010235 | ||||||
chr1:12010515
|
G | T | 12 | a0001c0001t0001g0173a0001c0001t0004g0016a0001c0001t0004g0048others(9): Show | 14 | HG01884.hp2 HG02280.hp2 HG02572.hp2 others(11): Show |
intron_variant | MODIFIER | c.2204+789G>T | MFN2 | ENSG00000116688.18 | transcript | ENST00000235329.10 | protein_coding | 18/18 | chr1 | 12010515 | ||||||
chr1:12010855
|
G | C | 12 | a0001c0001t0001g0173a0001c0001t0004g0016a0001c0001t0004g0048others(9): Show | 14 | HG01884.hp2 HG02280.hp2 HG02572.hp2 others(11): Show |
intron_variant | MODIFIER | c.2205-641G>C | MFN2 | ENSG00000116688.18 | transcript | ENST00000235329.10 | protein_coding | 18/18 | chr1 | 12010855 | ||||||
chr1:12010863
|
T | C | 219 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0009others(216): Show | 254 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(251): Show |
intron_variant | MODIFIER | c.2205-633T>C | MFN2 | ENSG00000116688.18 | transcript | ENST00000235329.10 | protein_coding | 18/18 | chr1 | 12010863 | ||||||
chr1:12010919
|
C | T | 7 | a0001c0003t0007g0035a0001c0003t0007g0280a0001c0003t0007g0281others(4): Show | 8 | HG01109.hp1 HG01167.hp1 HG02145.hp2 others(5): Show |
intron_variant | MODIFIER | c.2205-577C>T | MFN2 | ENSG00000116688.18 | transcript | ENST00000235329.10 | protein_coding | 18/18 | chr1 | 12010919 | ||||||
chr1:12011025
|
GC | G | 35 | a0001c0002t0005g0033a0001c0002t0005g0055a0001c0002t0005g0089others(32): Show | 38 | HG00408.hp1 HG00733.hp2 HG01109.hp1 others(35): Show |
intron_variant | MODIFIER | c.2205-463delC | MFN2 | ENSG00000116688.18 | transcript | ENST00000235329.10 | protein_coding | 18/18 | INFO_REALIGN_3_PRIME | chr1 | 12011025 | |||||
chr1:12011033
|
C | T | 20 | a0001c0002t0005g0033a0001c0002t0005g0089a0001c0002t0005g0190others(17): Show | 21 | HG00408.hp1 HG00733.hp2 HG01192.hp1 others(18): Show |
intron_variant | MODIFIER | c.2205-463C>T | MFN2 | ENSG00000116688.18 | transcript | ENST00000235329.10 | protein_coding | 18/18 | chr1 | 12011033 | ||||||
chr1:12011035
|
C | T | 28 | a0001c0002t0005g0033a0001c0002t0005g0055a0001c0002t0005g0089others(25): Show | 30 | HG00408.hp1 HG00733.hp2 HG01192.hp1 others(27): Show |
intron_variant | MODIFIER | c.2205-461C>T | MFN2 | ENSG00000116688.18 | transcript | ENST00000235329.10 | protein_coding | 18/18 | chr1 | 12011035 | ||||||
chr1:12011376
|
C | G | 72 | a0001c0001t0001g0237a0001c0001t0003g0003a0001c0001t0003g0031others(69): Show | 78 | HG00280.hp2 HG00408.hp2 HG00423.hp1 others(75): Show |
intron_variant | MODIFIER | c.2205-120C>G | MFN2 | ENSG00000116688.18 | transcript | ENST00000235329.10 | protein_coding | 18/18 | chr1 | 12011376 | ||||||
chr1:12011458
|
T | G | 1 | a0001c0001t0021g0184 | 1 | NA18978.hp1 | intron_variant | MODIFIER | c.2205-38T>G | MFN2 | ENSG00000116688.18 | transcript | ENST00000235329.10 | protein_coding | 18/18 | chr1 | 12011458 | ||||||
chr1:12011478
|
A | G | 1 | a0001c0001t0021g0184 | 1 | NA18978.hp1 | intron_variant | MODIFIER | c.2205-18A>G | MFN2 | ENSG00000116688.18 | transcript | ENST00000235329.10 | protein_coding | 18/18 | chr1 | 12011478 | ||||||
chr1:12011479
|
G | C | 1 | a0001c0001t0021g0184 | 1 | NA18978.hp1 | intron_variant | MODIFIER | c.2205-17G>C | MFN2 | ENSG00000116688.18 | transcript | ENST00000235329.10 | protein_coding | 18/18 | chr1 | 12011479 | ||||||
chr1:12011481
|
A | C | 1 | a0001c0001t0021g0184 | 1 | NA18978.hp1 | intron_variant | MODIFIER | c.2205-15A>C | MFN2 | ENSG00000116688.18 | transcript | ENST00000235329.10 | protein_coding | 18/18 | chr1 | 12011481 | ||||||
chr1:12011482
|
C | A | 1 | a0001c0001t0021g0184 | 1 | NA18978.hp1 | intron_variant | MODIFIER | c.2205-14C>A | MFN2 | ENSG00000116688.18 | transcript | ENST00000235329.10 | protein_coding | 18/18 | chr1 | 12011482 | ||||||
chr1:12011483
|
C | A | 7 | a0001c0001t0004g0296a0001c0001t0004g0297a0001c0001t0004g0298others(4): Show | 7 | HG02630.hp2 HG02895.hp2 HG03195.hp2 others(4): Show |
intron_variant | MODIFIER | c.2205-13C>A | MFN2 | ENSG00000116688.18 | transcript | ENST00000235329.10 | protein_coding | 18/18 | chr1 | 12011483 |