geneid | 84340 |
---|---|
ensemblid | ENSG00000164347.18 |
hgncid | 29682 |
symbol | GFM2 |
name | GTP dependent ribosome recycling factor mitochondrial 2 |
refseq_nuc | NM_032380.5 |
refseq_prot | NP_115756.2 |
ensembl_nuc | ENST00000296805.8 |
ensembl_prot | ENSP00000296805.3 |
mane_status | MANE Select |
chr | chr5 |
start | 74721206 |
end | 74767117 |
strand | - |
ver | v1.2 |
region | chr5:74721206-74767117 |
region5000 | chr5:74716206-74772117 |
regionname0 | GFM2_chr5_74721206_74767117 |
regionname5000 | GFM2_chr5_74716206_74772117 |
ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 1/0 | 779 | 201 | 25 | 42 | 98 | 9 | 26 | 69 | GFM2_chr5_74716206_74772117 | GFM2 | copy fasta | chr5 | 74716206 | 74772117 |
a0002 | 0/0 | 777 | 97 | 43 | 16 | 33 | 1 | 4 | 23 | GFM2_chr5_74716206_74772117 | GFM2 | copy fasta | chr5 | 74716206 | 74772117 |
a0003 | 0/1 | 777 | 31 | 9 | 10 | 2 | 4 | 5 | 2 | GFM2_chr5_74716206_74772117 | GFM2 | copy fasta | chr5 | 74716206 | 74772117 |
a0004 | 0/0 | 779 | 13 | 0 | 0 | 13 | 0 | 0 | 13 | GFM2_chr5_74716206_74772117 | GFM2 | copy fasta | chr5 | 74716206 | 74772117 |
a0005 | 0/0 | 777 | 11 | 9 | 2 | 0 | 0 | 0 | 0 | GFM2_chr5_74716206_74772117 | GFM2 | copy fasta | chr5 | 74716206 | 74772117 |
a0006 | 0/0 | 777 | 4 | 0 | 2 | 2 | 0 | 0 | 1 | GFM2_chr5_74716206_74772117 | GFM2 | copy fasta | chr5 | 74716206 | 74772117 |
a0007 | 0/0 | 779 | 3 | 0 | 0 | 3 | 0 | 0 | 3 | GFM2_chr5_74716206_74772117 | GFM2 | copy fasta | chr5 | 74716206 | 74772117 |
a0008 | 0/0 | 777 | 2 | 1 | 1 | 0 | 0 | 0 | 0 | GFM2_chr5_74716206_74772117 | GFM2 | copy fasta | chr5 | 74716206 | 74772117 |
a0009 | 0/0 | 777 | 2 | 1 | 1 | 0 | 0 | 0 | 0 | GFM2_chr5_74716206_74772117 | GFM2 | copy fasta | chr5 | 74716206 | 74772117 |
a0010 | 0/0 | 779 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | GFM2_chr5_74716206_74772117 | GFM2 | copy fasta | chr5 | 74716206 | 74772117 |
a0011 | 0/0 | 777 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | GFM2_chr5_74716206_74772117 | GFM2 | copy fasta | chr5 | 74716206 | 74772117 |
a0012 | 0/0 | 777 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | GFM2_chr5_74716206_74772117 | GFM2 | copy fasta | chr5 | 74716206 | 74772117 |
a0013 | 0/0 | 779 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | GFM2_chr5_74716206_74772117 | GFM2 | copy fasta | chr5 | 74716206 | 74772117 |
a0014 | 0/0 | 777 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | GFM2_chr5_74716206_74772117 | GFM2 | copy fasta | chr5 | 74716206 | 74772117 |
a0015 | 0/0 | 777 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | GFM2_chr5_74716206_74772117 | GFM2 | copy fasta | chr5 | 74716206 | 74772117 |
a0016 | 0/0 | 779 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | GFM2_chr5_74716206_74772117 | GFM2 | copy fasta | chr5 | 74716206 | 74772117 |
a0017 | 0/0 | 779 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | GFM2_chr5_74716206_74772117 | GFM2 | copy fasta | chr5 | 74716206 | 74772117 |
chapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
c0001 | 1/0 | 2340 | 198 | 25 | 42 | 95 | 9 | 26 | GFM2_chr5_74716206_74772117 | GFM2 | copy fasta | chr5 | 74716206 | 74772117 |
c0002 | 0/0 | 2334 | 73 | 19 | 16 | 33 | 1 | 4 | GFM2_chr5_74716206_74772117 | GFM2 | copy fasta | chr5 | 74716206 | 74772117 |
c0003 | 0/1 | 2334 | 31 | 9 | 10 | 2 | 4 | 5 | GFM2_chr5_74716206_74772117 | GFM2 | copy fasta | chr5 | 74716206 | 74772117 |
c0004 | 0/0 | 2340 | 13 | 0 | 0 | 13 | 0 | 0 | GFM2_chr5_74716206_74772117 | GFM2 | copy fasta | chr5 | 74716206 | 74772117 |
c0005 | 0/0 | 2334 | 13 | 13 | 0 | 0 | 0 | 0 | GFM2_chr5_74716206_74772117 | GFM2 | copy fasta | chr5 | 74716206 | 74772117 |
c0006 | 0/0 | 2334 | 11 | 11 | 0 | 0 | 0 | 0 | GFM2_chr5_74716206_74772117 | GFM2 | copy fasta | chr5 | 74716206 | 74772117 |
c0007 | 0/0 | 2334 | 7 | 5 | 2 | 0 | 0 | 0 | GFM2_chr5_74716206_74772117 | GFM2 | copy fasta | chr5 | 74716206 | 74772117 |
c0008 | 0/0 | 2334 | 4 | 0 | 2 | 2 | 0 | 0 | GFM2_chr5_74716206_74772117 | GFM2 | copy fasta | chr5 | 74716206 | 74772117 |
c0009 | 0/0 | 2334 | 4 | 4 | 0 | 0 | 0 | 0 | GFM2_chr5_74716206_74772117 | GFM2 | copy fasta | chr5 | 74716206 | 74772117 |
c0010 | 0/0 | 2340 | 3 | 0 | 0 | 3 | 0 | 0 | GFM2_chr5_74716206_74772117 | GFM2 | copy fasta | chr5 | 74716206 | 74772117 |
c0011 | 0/0 | 2340 | 2 | 0 | 0 | 2 | 0 | 0 | GFM2_chr5_74716206_74772117 | GFM2 | copy fasta | chr5 | 74716206 | 74772117 |
c0012 | 0/0 | 2334 | 2 | 1 | 1 | 0 | 0 | 0 | GFM2_chr5_74716206_74772117 | GFM2 | copy fasta | chr5 | 74716206 | 74772117 |
c0013 | 0/0 | 2334 | 2 | 1 | 1 | 0 | 0 | 0 | GFM2_chr5_74716206_74772117 | GFM2 | copy fasta | chr5 | 74716206 | 74772117 |
c0014 | 0/0 | 2340 | 1 | 0 | 0 | 1 | 0 | 0 | GFM2_chr5_74716206_74772117 | GFM2 | copy fasta | chr5 | 74716206 | 74772117 |
c0015 | 0/0 | 2334 | 1 | 0 | 0 | 1 | 0 | 0 | GFM2_chr5_74716206_74772117 | GFM2 | copy fasta | chr5 | 74716206 | 74772117 |
c0016 | 0/0 | 2334 | 1 | 0 | 0 | 0 | 0 | 1 | GFM2_chr5_74716206_74772117 | GFM2 | copy fasta | chr5 | 74716206 | 74772117 |
c0017 | 0/0 | 2334 | 1 | 1 | 0 | 0 | 0 | 0 | GFM2_chr5_74716206_74772117 | GFM2 | copy fasta | chr5 | 74716206 | 74772117 |
c0018 | 0/0 | 2340 | 1 | 0 | 0 | 1 | 0 | 0 | GFM2_chr5_74716206_74772117 | GFM2 | copy fasta | chr5 | 74716206 | 74772117 |
c0019 | 0/0 | 2334 | 1 | 1 | 0 | 0 | 0 | 0 | GFM2_chr5_74716206_74772117 | GFM2 | copy fasta | chr5 | 74716206 | 74772117 |
c0020 | 0/0 | 2340 | 1 | 0 | 0 | 1 | 0 | 0 | GFM2_chr5_74716206_74772117 | GFM2 | copy fasta | chr5 | 74716206 | 74772117 |
c0021 | 0/0 | 2340 | 1 | 0 | 1 | 0 | 0 | 0 | GFM2_chr5_74716206_74772117 | GFM2 | copy fasta | chr5 | 74716206 | 74772117 |
c0022 | 0/0 | 2340 | 1 | 0 | 1 | 0 | 0 | 0 | GFM2_chr5_74716206_74772117 | GFM2 | copy fasta | chr5 | 74716206 | 74772117 |
thapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
t0001 | 1/1 | 654 | 282 | 87 | 56 | 94 | 12 | 31 | GFM2_chr5_74716206_74772117 | GFM2 | copy fasta | chr5 | 74716206 | 74772117 |
t0002 | 0/0 | 654 | 56 | 2 | 13 | 35 | 1 | 5 | GFM2_chr5_74716206_74772117 | GFM2 | copy fasta | chr5 | 74716206 | 74772117 |
t0003 | 0/0 | 652 | 33 | 1 | 7 | 24 | 1 | 0 | GFM2_chr5_74716206_74772117 | GFM2 | copy fasta | chr5 | 74716206 | 74772117 |
t0004 | 0/0 | 654 | 1 | 0 | 0 | 1 | 0 | 0 | GFM2_chr5_74716206_74772117 | GFM2 | copy fasta | chr5 | 74716206 | 74772117 |
ghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
g0001 | 1/0 | 6 | 0 | 2 | 3 | 0 | 0 | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
g0002 | 0/0 | 5 | 0 | 3 | 1 | 0 | 1 | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
g0003 | 0/0 | 5 | 0 | 4 | 1 | 0 | 0 | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
g0004 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
g0005 | 0/0 | 4 | 0 | 1 | 2 | 0 | 1 | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
g0006 | 0/0 | 4 | 0 | 2 | 1 | 1 | 0 | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
g0007 | 0/0 | 3 | 0 | 1 | 1 | 0 | 1 | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
g0008 | 0/0 | 3 | 2 | 0 | 1 | 0 | 0 | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
g0009 | 0/0 | 3 | 0 | 0 | 0 | 2 | 1 | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
g0010 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
g0011 | 0/0 | 3 | 2 | 1 | 0 | 0 | 0 | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
g0012 | 0/0 | 3 | 0 | 1 | 0 | 2 | 0 | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
g0013 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
g0014 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
g0015 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
g0016 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
g0017 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
g0018 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
g0019 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
g0020 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
g0021 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
g0022 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
g0023 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
g0024 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
g0025 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
g0026 | 0/0 | 2 | 0 | 0 | 0 | 1 | 1 | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
g0027 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
g0028 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
g0029 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
g0030 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
g0031 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
g0032 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
g0033 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
g0034 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
g0035 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
g0036 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
g0037 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
g0038 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
g0039 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
g0040 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
g0045 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
g0051 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
g0053 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
g0054 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
g0060 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
g0061 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
g0064 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
g0072 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
g0076 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
g0080 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
g0081 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
g0085 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
g0088 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
g0091 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
g0092 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
g0093 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
g0095 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
g0096 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
g0101 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
g0102 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
g0103 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
g0105 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
g0107 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
g0108 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
g0109 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
g0111 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
g0112 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
g0113 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
g0114 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
g0122 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
g0125 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
g0128 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
g0150 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
g0158 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
g0161 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
g0162 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
g0163 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
g0165 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
g0168 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
g0169 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
g0171 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
g0172 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
g0177 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
g0182 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
g0184 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
g0187 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
g0191 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
g0192 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
g0193 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
g0198 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
g0199 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
g0203 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
g0206 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
g0207 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
g0208 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
g0209 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
g0210 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
g0211 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
g0220 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
g0223 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
g0227 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
g0251 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
g0254 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
g0255 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
g0266 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
g0267 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
g0268 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
g0269 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
g0270 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
g0271 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
g0272 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
g0273 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
g0274 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
g0275 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
g0276 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
g0277 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
g0278 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
g0279 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
g0280 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
g0281 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
g0282 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
g0284 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
g0285 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
g0286 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
g0287 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
g0288 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
g0289 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
g0290 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
g0291 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
g0292 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
g0293 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
g0294 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
g0296 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
g0297 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
g0298 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
g0299 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
g0300 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
g0302 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
g0303 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
g0305 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
g0306 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
g0307 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
g0308 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
g0309 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
g0310 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
achapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 1/0 | 2340 | 198 | 25 | 42 | 95 | 9 | 26 | GFM2_chr5_74716206_74772117 | GFM2 | copy fasta | chr5 | 74716206 | 74772117 |
a0001c0011 | 0/0 | 2340 | 2 | 0 | 0 | 2 | 0 | 0 | GFM2_chr5_74716206_74772117 | GFM2 | copy fasta | chr5 | 74716206 | 74772117 |
a0001c0020 | 0/0 | 2340 | 1 | 0 | 0 | 1 | 0 | 0 | GFM2_chr5_74716206_74772117 | GFM2 | copy fasta | chr5 | 74716206 | 74772117 |
a0002c0002 | 0/0 | 2334 | 73 | 19 | 16 | 33 | 1 | 4 | GFM2_chr5_74716206_74772117 | GFM2 | copy fasta | chr5 | 74716206 | 74772117 |
a0002c0005 | 0/0 | 2334 | 13 | 13 | 0 | 0 | 0 | 0 | GFM2_chr5_74716206_74772117 | GFM2 | copy fasta | chr5 | 74716206 | 74772117 |
a0002c0006 | 0/0 | 2334 | 11 | 11 | 0 | 0 | 0 | 0 | GFM2_chr5_74716206_74772117 | GFM2 | copy fasta | chr5 | 74716206 | 74772117 |
a0003c0003 | 0/1 | 2334 | 31 | 9 | 10 | 2 | 4 | 5 | GFM2_chr5_74716206_74772117 | GFM2 | copy fasta | chr5 | 74716206 | 74772117 |
a0004c0004 | 0/0 | 2340 | 13 | 0 | 0 | 13 | 0 | 0 | GFM2_chr5_74716206_74772117 | GFM2 | copy fasta | chr5 | 74716206 | 74772117 |
a0005c0007 | 0/0 | 2334 | 7 | 5 | 2 | 0 | 0 | 0 | GFM2_chr5_74716206_74772117 | GFM2 | copy fasta | chr5 | 74716206 | 74772117 |
a0005c0009 | 0/0 | 2334 | 4 | 4 | 0 | 0 | 0 | 0 | GFM2_chr5_74716206_74772117 | GFM2 | copy fasta | chr5 | 74716206 | 74772117 |
a0006c0008 | 0/0 | 2334 | 4 | 0 | 2 | 2 | 0 | 0 | GFM2_chr5_74716206_74772117 | GFM2 | copy fasta | chr5 | 74716206 | 74772117 |
a0007c0010 | 0/0 | 2340 | 3 | 0 | 0 | 3 | 0 | 0 | GFM2_chr5_74716206_74772117 | GFM2 | copy fasta | chr5 | 74716206 | 74772117 |
a0008c0013 | 0/0 | 2334 | 2 | 1 | 1 | 0 | 0 | 0 | GFM2_chr5_74716206_74772117 | GFM2 | copy fasta | chr5 | 74716206 | 74772117 |
a0009c0012 | 0/0 | 2334 | 2 | 1 | 1 | 0 | 0 | 0 | GFM2_chr5_74716206_74772117 | GFM2 | copy fasta | chr5 | 74716206 | 74772117 |
a0010c0018 | 0/0 | 2340 | 1 | 0 | 0 | 1 | 0 | 0 | GFM2_chr5_74716206_74772117 | GFM2 | copy fasta | chr5 | 74716206 | 74772117 |
a0011c0017 | 0/0 | 2334 | 1 | 1 | 0 | 0 | 0 | 0 | GFM2_chr5_74716206_74772117 | GFM2 | copy fasta | chr5 | 74716206 | 74772117 |
a0012c0019 | 0/0 | 2334 | 1 | 1 | 0 | 0 | 0 | 0 | GFM2_chr5_74716206_74772117 | GFM2 | copy fasta | chr5 | 74716206 | 74772117 |
a0013c0021 | 0/0 | 2340 | 1 | 0 | 1 | 0 | 0 | 0 | GFM2_chr5_74716206_74772117 | GFM2 | copy fasta | chr5 | 74716206 | 74772117 |
a0014c0016 | 0/0 | 2334 | 1 | 0 | 0 | 0 | 0 | 1 | GFM2_chr5_74716206_74772117 | GFM2 | copy fasta | chr5 | 74716206 | 74772117 |
a0015c0015 | 0/0 | 2334 | 1 | 0 | 0 | 1 | 0 | 0 | GFM2_chr5_74716206_74772117 | GFM2 | copy fasta | chr5 | 74716206 | 74772117 |
a0016c0014 | 0/0 | 2340 | 1 | 0 | 0 | 1 | 0 | 0 | GFM2_chr5_74716206_74772117 | GFM2 | copy fasta | chr5 | 74716206 | 74772117 |
a0017c0022 | 0/0 | 2340 | 1 | 0 | 1 | 0 | 0 | 0 | GFM2_chr5_74716206_74772117 | GFM2 | copy fasta | chr5 | 74716206 | 74772117 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 1/0 | 2993 | 179 | 24 | 36 | 84 | 8 | 26 | GFM2_chr5_74716206_74772117 | GFM2 | copy fasta | chr5 | 74716206 | 74772117 |
a0001c0001t0003 | 0/0 | 2991 | 19 | 1 | 6 | 11 | 1 | 0 | GFM2_chr5_74716206_74772117 | GFM2 | copy fasta | chr5 | 74716206 | 74772117 |
a0001c0011t0002 | 0/0 | 2993 | 2 | 0 | 0 | 2 | 0 | 0 | GFM2_chr5_74716206_74772117 | GFM2 | copy fasta | chr5 | 74716206 | 74772117 |
a0001c0020t0001 | 0/0 | 2993 | 1 | 0 | 0 | 1 | 0 | 0 | GFM2_chr5_74716206_74772117 | GFM2 | copy fasta | chr5 | 74716206 | 74772117 |
a0002c0002t0001 | 0/0 | 2987 | 20 | 17 | 3 | 0 | 0 | 0 | GFM2_chr5_74716206_74772117 | GFM2 | copy fasta | chr5 | 74716206 | 74772117 |
a0002c0002t0002 | 0/0 | 2987 | 52 | 2 | 13 | 32 | 1 | 4 | GFM2_chr5_74716206_74772117 | GFM2 | copy fasta | chr5 | 74716206 | 74772117 |
a0002c0002t0004 | 0/0 | 2987 | 1 | 0 | 0 | 1 | 0 | 0 | GFM2_chr5_74716206_74772117 | GFM2 | copy fasta | chr5 | 74716206 | 74772117 |
a0002c0005t0001 | 0/0 | 2987 | 13 | 13 | 0 | 0 | 0 | 0 | GFM2_chr5_74716206_74772117 | GFM2 | copy fasta | chr5 | 74716206 | 74772117 |
a0002c0006t0001 | 0/0 | 2987 | 11 | 11 | 0 | 0 | 0 | 0 | GFM2_chr5_74716206_74772117 | GFM2 | copy fasta | chr5 | 74716206 | 74772117 |
a0003c0003t0001 | 0/1 | 2987 | 31 | 9 | 10 | 2 | 4 | 5 | GFM2_chr5_74716206_74772117 | GFM2 | copy fasta | chr5 | 74716206 | 74772117 |
a0004c0004t0001 | 0/0 | 2993 | 1 | 0 | 0 | 1 | 0 | 0 | GFM2_chr5_74716206_74772117 | GFM2 | copy fasta | chr5 | 74716206 | 74772117 |
a0004c0004t0003 | 0/0 | 2991 | 12 | 0 | 0 | 12 | 0 | 0 | GFM2_chr5_74716206_74772117 | GFM2 | copy fasta | chr5 | 74716206 | 74772117 |
a0005c0007t0001 | 0/0 | 2987 | 7 | 5 | 2 | 0 | 0 | 0 | GFM2_chr5_74716206_74772117 | GFM2 | copy fasta | chr5 | 74716206 | 74772117 |
a0005c0009t0001 | 0/0 | 2987 | 4 | 4 | 0 | 0 | 0 | 0 | GFM2_chr5_74716206_74772117 | GFM2 | copy fasta | chr5 | 74716206 | 74772117 |
a0006c0008t0001 | 0/0 | 2987 | 4 | 0 | 2 | 2 | 0 | 0 | GFM2_chr5_74716206_74772117 | GFM2 | copy fasta | chr5 | 74716206 | 74772117 |
a0007c0010t0001 | 0/0 | 2993 | 3 | 0 | 0 | 3 | 0 | 0 | GFM2_chr5_74716206_74772117 | GFM2 | copy fasta | chr5 | 74716206 | 74772117 |
a0008c0013t0001 | 0/0 | 2987 | 2 | 1 | 1 | 0 | 0 | 0 | GFM2_chr5_74716206_74772117 | GFM2 | copy fasta | chr5 | 74716206 | 74772117 |
a0009c0012t0001 | 0/0 | 2987 | 2 | 1 | 1 | 0 | 0 | 0 | GFM2_chr5_74716206_74772117 | GFM2 | copy fasta | chr5 | 74716206 | 74772117 |
a0010c0018t0001 | 0/0 | 2993 | 1 | 0 | 0 | 1 | 0 | 0 | GFM2_chr5_74716206_74772117 | GFM2 | copy fasta | chr5 | 74716206 | 74772117 |
a0011c0017t0001 | 0/0 | 2987 | 1 | 1 | 0 | 0 | 0 | 0 | GFM2_chr5_74716206_74772117 | GFM2 | copy fasta | chr5 | 74716206 | 74772117 |
a0012c0019t0001 | 0/0 | 2987 | 1 | 1 | 0 | 0 | 0 | 0 | GFM2_chr5_74716206_74772117 | GFM2 | copy fasta | chr5 | 74716206 | 74772117 |
a0013c0021t0001 | 0/0 | 2993 | 1 | 0 | 1 | 0 | 0 | 0 | GFM2_chr5_74716206_74772117 | GFM2 | copy fasta | chr5 | 74716206 | 74772117 |
a0014c0016t0002 | 0/0 | 2987 | 1 | 0 | 0 | 0 | 0 | 1 | GFM2_chr5_74716206_74772117 | GFM2 | copy fasta | chr5 | 74716206 | 74772117 |
a0015c0015t0002 | 0/0 | 2987 | 1 | 0 | 0 | 1 | 0 | 0 | GFM2_chr5_74716206_74772117 | GFM2 | copy fasta | chr5 | 74716206 | 74772117 |
a0016c0014t0003 | 0/0 | 2991 | 1 | 0 | 0 | 1 | 0 | 0 | GFM2_chr5_74716206_74772117 | GFM2 | copy fasta | chr5 | 74716206 | 74772117 |
a0017c0022t0003 | 0/0 | 2991 | 1 | 0 | 1 | 0 | 0 | 0 | GFM2_chr5_74716206_74772117 | GFM2 | copy fasta | chr5 | 74716206 | 74772117 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0001 | 1/0 | 6 | 0 | 2 | 3 | 0 | 0 | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
a0001c0001t0001g0003 | 0/0 | 5 | 0 | 4 | 1 | 0 | 0 | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
a0001c0001t0001g0004 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
a0001c0001t0001g0005 | 0/0 | 4 | 0 | 1 | 2 | 0 | 1 | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
a0001c0001t0001g0008 | 0/0 | 3 | 2 | 0 | 1 | 0 | 0 | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
a0001c0001t0001g0009 | 0/0 | 3 | 0 | 0 | 0 | 2 | 1 | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
a0001c0001t0001g0016 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
a0001c0001t0001g0017 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
a0001c0001t0001g0018 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
a0001c0001t0001g0021 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
a0001c0001t0001g0022 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
a0001c0001t0001g0023 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
a0001c0001t0001g0024 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
a0001c0001t0001g0025 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
a0001c0001t0001g0026 | 0/0 | 2 | 0 | 0 | 0 | 1 | 1 | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
a0001c0001t0001g0027 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
a0001c0001t0001g0028 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
a0001c0001t0001g0029 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
a0001c0001t0001g0030 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
a0001c0001t0001g0031 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
a0001c0001t0001g0032 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
a0001c0001t0001g0033 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
a0001c0001t0001g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
a0001c0001t0001g0085 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
a0001c0001t0001g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
a0001c0001t0001g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
a0001c0001t0001g0088 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
a0001c0001t0001g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
a0001c0001t0001g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
a0001c0001t0001g0091 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
a0001c0001t0001g0092 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
a0001c0001t0001g0093 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
a0001c0001t0001g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
a0001c0001t0001g0095 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
a0001c0001t0001g0096 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
a0001c0001t0001g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
a0001c0001t0001g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
a0001c0001t0001g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
a0001c0001t0001g0101 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
a0001c0001t0001g0102 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
a0001c0001t0001g0103 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
a0001c0001t0001g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
a0001c0001t0001g0105 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
a0001c0001t0001g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
a0001c0001t0001g0107 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
a0001c0001t0001g0108 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
a0001c0001t0001g0109 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
a0001c0001t0001g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
a0001c0001t0001g0111 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
a0001c0001t0001g0112 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
a0001c0001t0001g0113 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
a0001c0001t0001g0114 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
a0001c0001t0001g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
a0001c0001t0001g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
a0001c0001t0001g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
a0001c0001t0001g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
a0001c0001t0001g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
a0001c0001t0001g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
a0001c0001t0001g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
a0001c0001t0001g0122 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
a0001c0001t0001g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
a0001c0001t0001g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
a0001c0001t0001g0125 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
a0001c0001t0001g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
a0001c0001t0001g0128 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
a0001c0001t0001g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
a0001c0001t0001g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
a0001c0001t0001g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
a0001c0001t0001g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
a0001c0001t0001g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
a0001c0001t0001g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
a0001c0001t0001g0158 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
a0001c0001t0001g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
a0001c0001t0001g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
a0001c0001t0001g0161 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
a0001c0001t0001g0162 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
a0001c0001t0001g0163 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
a0001c0001t0001g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
a0001c0001t0001g0165 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
a0001c0001t0001g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
a0001c0001t0001g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
a0001c0001t0001g0168 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
a0001c0001t0001g0169 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
a0001c0001t0001g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
a0001c0001t0001g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
a0001c0001t0001g0177 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
a0001c0001t0001g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
a0001c0001t0001g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
a0001c0001t0001g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
a0001c0001t0001g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
a0001c0001t0001g0182 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
a0001c0001t0001g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
a0001c0001t0001g0184 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
a0001c0001t0001g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
a0001c0001t0001g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
a0001c0001t0001g0187 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
a0001c0001t0001g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
a0001c0001t0001g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
a0001c0001t0001g0191 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
a0001c0001t0001g0192 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
a0001c0001t0001g0193 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
a0001c0001t0001g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
a0001c0001t0001g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
a0001c0001t0001g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
a0001c0001t0001g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
a0001c0001t0001g0198 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
a0001c0001t0001g0199 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
a0001c0001t0001g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
a0001c0001t0001g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
a0001c0001t0001g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
a0001c0001t0001g0203 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
a0001c0001t0001g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
a0001c0001t0001g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
a0001c0001t0001g0206 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
a0001c0001t0001g0207 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
a0001c0001t0001g0209 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
a0001c0001t0001g0210 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
a0001c0001t0001g0211 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
a0001c0001t0001g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
a0001c0001t0001g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
a0001c0001t0001g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
a0001c0001t0001g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
a0001c0001t0001g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
a0001c0001t0001g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
a0001c0001t0001g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
a0001c0001t0001g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
a0001c0001t0001g0220 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
a0001c0001t0001g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
a0001c0001t0001g0223 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
a0001c0001t0001g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
a0001c0001t0001g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
a0001c0001t0001g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
a0001c0001t0001g0227 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
a0001c0001t0001g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
a0001c0001t0001g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
a0001c0001t0001g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
a0001c0001t0001g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
a0001c0001t0001g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
a0001c0001t0001g0254 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
a0001c0001t0001g0300 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
a0001c0001t0001g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
a0001c0001t0001g0303 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
a0001c0001t0001g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
a0001c0001t0001g0305 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
a0001c0001t0003g0006 | 0/0 | 4 | 0 | 2 | 1 | 1 | 0 | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
a0001c0001t0003g0035 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
a0001c0001t0003g0036 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
a0001c0001t0003g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
a0001c0001t0003g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
a0001c0001t0003g0251 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
a0001c0001t0003g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
a0001c0001t0003g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
a0001c0001t0003g0255 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
a0001c0001t0003g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
a0001c0001t0003g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
a0001c0001t0003g0266 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
a0001c0001t0003g0267 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
a0001c0001t0003g0268 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
a0001c0011t0002g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
a0001c0011t0002g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
a0001c0020t0001g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
a0002c0002t0001g0019 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
a0002c0002t0001g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
a0002c0002t0001g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
a0002c0002t0001g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
a0002c0002t0001g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
a0002c0002t0001g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
a0002c0002t0001g0150 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
a0002c0002t0001g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
a0002c0002t0001g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
a0002c0002t0001g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
a0002c0002t0001g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
a0002c0002t0001g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
a0002c0002t0001g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
a0002c0002t0001g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
a0002c0002t0001g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
a0002c0002t0001g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
a0002c0002t0001g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
a0002c0002t0001g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
a0002c0002t0001g0302 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
a0002c0002t0002g0002 | 0/0 | 5 | 0 | 3 | 1 | 0 | 1 | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
a0002c0002t0002g0007 | 0/0 | 3 | 0 | 1 | 1 | 0 | 1 | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
a0002c0002t0002g0013 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
a0002c0002t0002g0014 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
a0002c0002t0002g0015 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
a0002c0002t0002g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
a0002c0002t0002g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
a0002c0002t0002g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
a0002c0002t0002g0045 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
a0002c0002t0002g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
a0002c0002t0002g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
a0002c0002t0002g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
a0002c0002t0002g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
a0002c0002t0002g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
a0002c0002t0002g0051 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
a0002c0002t0002g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
a0002c0002t0002g0054 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
a0002c0002t0002g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
a0002c0002t0002g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
a0002c0002t0002g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
a0002c0002t0002g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
a0002c0002t0002g0060 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
a0002c0002t0002g0061 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
a0002c0002t0002g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
a0002c0002t0002g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
a0002c0002t0002g0064 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
a0002c0002t0002g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
a0002c0002t0002g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
a0002c0002t0002g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
a0002c0002t0002g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
a0002c0002t0002g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
a0002c0002t0002g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
a0002c0002t0002g0072 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
a0002c0002t0002g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
a0002c0002t0002g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
a0002c0002t0002g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
a0002c0002t0002g0076 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
a0002c0002t0002g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
a0002c0002t0002g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
a0002c0002t0002g0080 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
a0002c0002t0002g0081 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
a0002c0002t0002g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
a0002c0002t0002g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
a0002c0002t0004g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
a0002c0005t0001g0034 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
a0002c0005t0001g0040 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
a0002c0005t0001g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
a0002c0005t0001g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
a0002c0005t0001g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
a0002c0005t0001g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
a0002c0005t0001g0306 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
a0002c0005t0001g0307 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
a0002c0005t0001g0308 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
a0002c0005t0001g0309 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
a0002c0005t0001g0310 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
a0002c0006t0001g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
a0002c0006t0001g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
a0002c0006t0001g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
a0002c0006t0001g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
a0002c0006t0001g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
a0002c0006t0001g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
a0002c0006t0001g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
a0002c0006t0001g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
a0002c0006t0001g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
a0002c0006t0001g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
a0002c0006t0001g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
a0003c0003t0001g0011 | 0/0 | 3 | 2 | 1 | 0 | 0 | 0 | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
a0003c0003t0001g0012 | 0/0 | 3 | 0 | 1 | 0 | 2 | 0 | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
a0003c0003t0001g0038 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
a0003c0003t0001g0039 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
a0003c0003t0001g0275 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
a0003c0003t0001g0276 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
a0003c0003t0001g0277 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
a0003c0003t0001g0278 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
a0003c0003t0001g0279 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
a0003c0003t0001g0280 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
a0003c0003t0001g0281 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
a0003c0003t0001g0282 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
a0003c0003t0001g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
a0003c0003t0001g0284 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
a0003c0003t0001g0285 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
a0003c0003t0001g0287 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
a0003c0003t0001g0288 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
a0003c0003t0001g0289 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
a0003c0003t0001g0290 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
a0003c0003t0001g0291 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
a0003c0003t0001g0292 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
a0003c0003t0001g0293 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
a0003c0003t0001g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
a0003c0003t0001g0296 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
a0003c0003t0001g0297 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
a0004c0004t0001g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
a0004c0004t0003g0010 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
a0004c0004t0003g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
a0004c0004t0003g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
a0004c0004t0003g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
a0004c0004t0003g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
a0004c0004t0003g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
a0004c0004t0003g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
a0004c0004t0003g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
a0004c0004t0003g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
a0004c0004t0003g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
a0005c0007t0001g0037 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
a0005c0007t0001g0270 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
a0005c0007t0001g0271 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
a0005c0007t0001g0272 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
a0005c0007t0001g0273 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
a0005c0007t0001g0274 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
a0005c0009t0001g0020 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
a0005c0009t0001g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
a0005c0009t0001g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
a0006c0008t0001g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
a0006c0008t0001g0171 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
a0006c0008t0001g0172 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
a0006c0008t0001g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
a0007c0010t0001g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
a0007c0010t0001g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
a0007c0010t0001g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
a0008c0013t0001g0294 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
a0008c0013t0001g0298 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
a0009c0012t0001g0286 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
a0009c0012t0001g0299 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
a0010c0018t0001g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
a0011c0017t0001g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
a0012c0019t0001g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
a0013c0021t0001g0208 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
a0014c0016t0002g0053 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
a0015c0015t0002g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
a0016c0014t0003g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
a0017c0022t0003g0269 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0001 | c0001 | t0001 | g0122 | EUR | GBR | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
HG00099 | hp2 | a0002 | c0002 | t0002 | g0081 | EUR | GBR | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
HG00140 | hp1 | a0003 | c0003 | t0001 | g0296 | EUR | GBR | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
HG00140 | hp2 | a0001 | c0001 | t0001 | g0103 | EUR | GBR | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
HG00280 | hp1 | a0001 | c0001 | t0001 | g0009 | EUR | FIN | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
HG00280 | hp2 | a0003 | c0003 | t0001 | g0292 | EUR | FIN | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
HG00323 | hp1 | a0001 | c0001 | t0001 | g0026 | EUR | FIN | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
HG00323 | hp2 | a0001 | c0001 | t0001 | g0109 | EUR | FIN | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
HG00408 | hp1 | a0001 | c0001 | t0001 | g0030 | EAS | CHS | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
HG00408 | hp2 | a0002 | c0002 | t0002 | g0066 | EAS | CHS | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
HG00438 | hp1 | a0001 | c0001 | t0001 | g0197 | EAS | CHS | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
HG00438 | hp2 | a0006 | c0008 | t0001 | g0134 | EAS | CHS | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
HG00558 | hp1 | a0002 | c0002 | t0002 | g0043 | EAS | CHS | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
HG00558 | hp2 | a0001 | c0001 | t0001 | g0216 | EAS | CHS | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
HG00609 | hp1 | a0001 | c0001 | t0001 | g0018 | EAS | CHS | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
HG00609 | hp2 | a0001 | c0001 | t0001 | g0304 | EAS | CHS | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
HG00621 | hp1 | a0001 | c0001 | t0001 | g0129 | EAS | CHS | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
HG00621 | hp2 | a0001 | c0001 | t0001 | g0098 | EAS | CHS | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
HG00642 | hp1 | a0001 | c0001 | t0001 | g0303 | AMR | PUR | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
HG00642 | hp2 | a0009 | c0012 | t0001 | g0299 | AMR | PUR | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
HG00673 | hp1 | a0001 | c0001 | t0003 | g0246 | EAS | CHS | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
HG00673 | hp2 | a0001 | c0001 | t0001 | g0033 | EAS | CHS | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
HG00733 | hp1 | a0001 | c0001 | t0001 | g0128 | AMR | PUR | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
HG00733 | hp2 | a0005 | c0007 | t0001 | g0273 | AMR | PUR | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
HG00735 | hp1 | a0001 | c0001 | t0001 | g0184 | AMR | PUR | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
HG00735 | hp2 | a0006 | c0008 | t0001 | g0171 | AMR | PUR | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
HG00738 | hp1 | a0001 | c0001 | t0001 | g0210 | AMR | PUR | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
HG00738 | hp2 | a0003 | c0003 | t0001 | g0275 | AMR | PUR | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
HG00741 | hp1 | a0001 | c0001 | t0003 | g0006 | AMR | PUR | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
HG00741 | hp2 | a0002 | c0002 | t0001 | g0019 | AMR | PUR | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
HG01069 | hp1 | a0003 | c0003 | t0001 | g0285 | AMR | PUR | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
HG01069 | hp2 | a0002 | c0002 | t0002 | g0080 | AMR | PUR | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
HG01071 | hp1 | a0003 | c0003 | t0001 | g0012 | AMR | PUR | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
HG01071 | hp2 | a0002 | c0002 | t0002 | g0082 | AMR | PUR | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
HG01074 | hp1 | a0001 | c0001 | t0001 | g0191 | AMR | PUR | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
HG01074 | hp2 | a0001 | c0001 | t0001 | g0102 | AMR | PUR | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
HG01081 | hp1 | a0003 | c0003 | t0001 | g0011 | AMR | PUR | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
HG01081 | hp2 | a0001 | c0001 | t0001 | g0016 | AMR | PUR | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
HG01099 | hp1 | a0001 | c0001 | t0001 | g0111 | AMR | PUR | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
HG01099 | hp2 | a0001 | c0001 | t0001 | g0211 | AMR | PUR | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
HG01106 | hp1 | a0002 | c0002 | t0001 | g0019 | AMR | PUR | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
HG01106 | hp2 | a0001 | c0001 | t0001 | g0016 | AMR | PUR | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
HG01109 | hp1 | a0002 | c0002 | t0002 | g0076 | AMR | PUR | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
HG01109 | hp2 | a0003 | c0003 | t0001 | g0288 | AMR | PUR | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
HG01167 | hp1 | a0002 | c0002 | t0001 | g0150 | AMR | PUR | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
HG01167 | hp2 | a0003 | c0003 | t0001 | g0284 | AMR | PUR | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
HG01168 | hp1 | a0001 | c0001 | t0001 | g0005 | AMR | PUR | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
HG01168 | hp2 | a0001 | c0001 | t0001 | g0097 | AMR | PUR | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
HG01169 | hp1 | a0003 | c0003 | t0001 | g0038 | AMR | PUR | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
HG01169 | hp2 | a0001 | c0001 | t0001 | g0112 | AMR | PUR | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
HG01175 | hp1 | a0002 | c0002 | t0002 | g0060 | AMR | PUR | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
HG01175 | hp2 | a0001 | c0001 | t0003 | g0266 | AMR | PUR | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
HG01243 | hp1 | a0005 | c0007 | t0001 | g0037 | AMR | PUR | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
HG01243 | hp2 | a0008 | c0013 | t0001 | g0298 | AMR | PUR | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
HG01255 | hp1 | a0001 | c0001 | t0001 | g0091 | AMR | CLM | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
HG01255 | hp2 | a0003 | c0003 | t0001 | g0290 | AMR | CLM | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
HG01257 | hp1 | a0001 | c0001 | t0001 | g0084 | AMR | CLM | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
HG01257 | hp2 | a0002 | c0002 | t0002 | g0002 | AMR | CLM | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
HG01258 | hp1 | a0002 | c0002 | t0002 | g0002 | AMR | CLM | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
HG01258 | hp2 | a0001 | c0001 | t0001 | g0105 | AMR | CLM | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
HG01261 | hp1 | a0001 | c0001 | t0001 | g0113 | AMR | CLM | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
HG01261 | hp2 | a0001 | c0001 | t0001 | g0017 | AMR | CLM | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
HG01346 | hp1 | a0001 | c0001 | t0001 | g0032 | AMR | CLM | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
HG01346 | hp2 | a0002 | c0002 | t0002 | g0072 | AMR | CLM | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
HG01361 | hp1 | a0003 | c0003 | t0001 | g0276 | AMR | CLM | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
HG01361 | hp2 | a0001 | c0001 | t0001 | g0168 | AMR | CLM | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
HG01433 | hp1 | a0001 | c0001 | t0001 | g0203 | AMR | CLM | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
HG01433 | hp2 | a0002 | c0002 | t0002 | g0007 | AMR | CLM | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
HG01496 | hp1 | a0001 | c0001 | t0001 | g0207 | AMR | CLM | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
HG01496 | hp2 | a0001 | c0001 | t0001 | g0031 | AMR | CLM | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
HG01515 | hp1 | a0001 | c0001 | t0001 | g0009 | EUR | IBS | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
HG01515 | hp2 | a0003 | c0003 | t0001 | g0012 | EUR | IBS | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
HG01516 | hp1 | a0003 | c0003 | t0001 | g0012 | EUR | IBS | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
HG01516 | hp2 | a0001 | c0001 | t0001 | g0096 | EUR | IBS | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
HG01884 | hp1 | a0001 | c0001 | t0001 | g0008 | AFR | ACB | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
HG01884 | hp2 | a0002 | c0002 | t0001 | g0238 | AFR | ACB | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
HG01891 | hp1 | a0002 | c0005 | t0001 | g0231 | AFR | ACB | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
HG01891 | hp2 | a0001 | c0001 | t0001 | g0023 | AFR | ACB | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
HG01928 | hp1 | a0001 | c0001 | t0001 | g0003 | AMR | PEL | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
HG01928 | hp2 | a0002 | c0002 | t0002 | g0061 | AMR | PEL | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
HG01934 | hp1 | a0001 | c0001 | t0001 | g0169 | AMR | PEL | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
HG01934 | hp2 | a0002 | c0002 | t0002 | g0045 | AMR | PEL | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
HG01943 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
HG01943 | hp2 | a0001 | c0001 | t0001 | g0125 | AMR | PEL | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
HG01952 | hp1 | a0013 | c0021 | t0001 | g0208 | AMR | PEL | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
HG01952 | hp2 | a0002 | c0002 | t0002 | g0014 | AMR | PEL | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
HG01975 | hp1 | a0001 | c0001 | t0001 | g0003 | AMR | PEL | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
HG01975 | hp2 | a0002 | c0002 | t0002 | g0002 | AMR | PEL | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
HG01978 | hp1 | a0017 | c0022 | t0003 | g0269 | AMR | PEL | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
HG01978 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
HG01981 | hp1 | a0001 | c0001 | t0001 | g0088 | AMR | PEL | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
HG01981 | hp2 | a0001 | c0001 | t0001 | g0165 | AMR | PEL | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
HG02004 | hp1 | a0001 | c0001 | t0001 | g0003 | AMR | PEL | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
HG02004 | hp2 | a0001 | c0001 | t0001 | g0206 | AMR | PEL | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
HG02015 | hp1 | a0002 | c0002 | t0002 | g0050 | EAS | KHV | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
HG02015 | hp2 | a0001 | c0001 | t0001 | g0195 | EAS | KHV | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
HG02040 | hp1 | a0001 | c0001 | t0001 | g0204 | EAS | KHV | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
HG02040 | hp2 | a0001 | c0001 | t0001 | g0086 | EAS | KHV | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
HG02056 | hp1 | a0002 | c0002 | t0002 | g0002 | EAS | KHV | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
HG02056 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
HG02071 | hp1 | a0001 | c0001 | t0001 | g0160 | EAS | KHV | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
HG02071 | hp2 | a0002 | c0002 | t0002 | g0056 | EAS | KHV | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
HG02074 | hp1 | a0001 | c0001 | t0001 | g0094 | EAS | KHV | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
HG02074 | hp2 | a0001 | c0001 | t0001 | g0219 | EAS | KHV | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
HG02080 | hp1 | a0002 | c0002 | t0002 | g0007 | EAS | KHV | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
HG02080 | hp2 | a0001 | c0001 | t0001 | g0130 | EAS | KHV | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
HG02083 | hp1 | a0002 | c0002 | t0002 | g0058 | EAS | KHV | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
HG02083 | hp2 | a0001 | c0020 | t0001 | g0099 | EAS | KHV | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
HG02129 | hp1 | a0001 | c0001 | t0001 | g0213 | EAS | KHV | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
HG02129 | hp2 | a0001 | c0001 | t0001 | g0106 | EAS | KHV | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
HG02132 | hp1 | a0001 | c0001 | t0001 | g0030 | EAS | KHV | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
HG02132 | hp2 | a0002 | c0002 | t0002 | g0014 | EAS | KHV | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
HG02135 | hp1 | a0001 | c0001 | t0001 | g0170 | EAS | KHV | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
HG02135 | hp2 | a0002 | c0002 | t0002 | g0075 | EAS | KHV | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
HG02145 | hp1 | a0001 | c0001 | t0001 | g0228 | AFR | ACB | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
HG02145 | hp2 | a0002 | c0005 | t0001 | g0307 | AFR | ACB | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
HG02148 | hp1 | a0003 | c0003 | t0001 | g0280 | AMR | PEL | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
HG02148 | hp2 | a0001 | c0001 | t0001 | g0158 | AMR | PEL | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
HG02155 | hp1 | a0002 | c0002 | t0002 | g0052 | EAS | CDX | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
HG02155 | hp2 | a0001 | c0001 | t0001 | g0236 | EAS | CDX | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
HG02165 | hp1 | a0001 | c0001 | t0001 | g0100 | EAS | CDX | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
HG02165 | hp2 | a0001 | c0001 | t0001 | g0119 | EAS | CDX | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
HG02258 | hp1 | a0002 | c0002 | t0001 | g0149 | AFR | ACB | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
HG02258 | hp2 | a0001 | c0001 | t0001 | g0235 | AFR | ACB | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
HG02273 | hp1 | a0001 | c0001 | t0001 | g0003 | AMR | PEL | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
HG02273 | hp2 | a0001 | c0001 | t0003 | g0255 | AMR | PEL | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
HG02280 | hp1 | a0002 | c0002 | t0001 | g0242 | AFR | ACB | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
HG02280 | hp2 | a0001 | c0001 | t0001 | g0017 | AFR | ACB | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
HG02293 | hp1 | a0006 | c0008 | t0001 | g0172 | AMR | PEL | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
HG02293 | hp2 | a0001 | c0001 | t0003 | g0006 | AMR | PEL | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
HG02300 | hp1 | a0001 | c0001 | t0003 | g0267 | AMR | PEL | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
HG02300 | hp2 | a0002 | c0002 | t0002 | g0064 | AMR | PEL | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
HG02451 | hp1 | a0005 | c0009 | t0001 | g0153 | AFR | ACB | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
HG02451 | hp2 | a0002 | c0005 | t0001 | g0034 | AFR | ACB | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
HG02523 | hp1 | a0001 | c0001 | t0001 | g0025 | EAS | KHV | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
HG02523 | hp2 | a0001 | c0001 | t0001 | g0186 | EAS | KHV | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
HG02572 | hp1 | a0001 | c0001 | t0001 | g0185 | AFR | GWD | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
HG02572 | hp2 | a0003 | c0003 | t0001 | g0278 | AFR | GWD | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
HG02615 | hp1 | a0001 | c0001 | t0001 | g0225 | AFR | GWD | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
HG02615 | hp2 | a0002 | c0006 | t0001 | g0143 | AFR | GWD | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
HG02630 | hp1 | a0003 | c0003 | t0001 | g0279 | AFR | GWD | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
HG02630 | hp2 | a0002 | c0005 | t0001 | g0244 | AFR | GWD | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
HG02647 | hp1 | a0002 | c0002 | t0001 | g0241 | AFR | GWD | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
HG02647 | hp2 | a0003 | c0003 | t0001 | g0011 | AFR | GWD | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
HG02683 | hp1 | a0001 | c0001 | t0001 | g0227 | SAS | PJL | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
HG02683 | hp2 | a0001 | c0001 | t0001 | g0220 | SAS | PJL | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
HG02717 | hp1 | a0005 | c0009 | t0001 | g0020 | AFR | GWD | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
HG02717 | hp2 | a0005 | c0007 | t0001 | g0270 | AFR | GWD | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
HG02723 | hp1 | a0002 | c0005 | t0001 | g0040 | AFR | GWD | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
HG02723 | hp2 | a0002 | c0006 | t0001 | g0138 | AFR | GWD | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
HG02735 | hp1 | a0003 | c0003 | t0001 | g0039 | SAS | PJL | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
HG02735 | hp2 | a0001 | c0001 | t0001 | g0209 | SAS | PJL | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
HG02738 | hp1 | a0001 | c0001 | t0001 | g0114 | SAS | PJL | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
HG02738 | hp2 | a0001 | c0001 | t0001 | g0198 | SAS | PJL | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
HG02809 | hp1 | a0002 | c0002 | t0001 | g0240 | AFR | GWD | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
HG02809 | hp2 | a0001 | c0001 | t0001 | g0021 | AFR | GWD | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
HG02818 | hp1 | a0002 | c0002 | t0001 | g0302 | AFR | GWD | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
HG02818 | hp2 | a0002 | c0002 | t0002 | g0068 | AFR | GWD | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
HG02886 | hp1 | a0002 | c0005 | t0001 | g0308 | AFR | GWD | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
HG02886 | hp2 | a0012 | c0019 | t0001 | g0144 | AFR | GWD | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
HG02895 | hp1 | a0002 | c0002 | t0001 | g0147 | AFR | GWD | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
HG02895 | hp2 | a0001 | c0001 | t0001 | g0230 | AFR | GWD | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
HG02896 | hp1 | a0002 | c0002 | t0001 | g0151 | AFR | GWD | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
HG02896 | hp2 | a0003 | c0003 | t0001 | g0289 | AFR | GWD | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
HG02897 | hp1 | a0003 | c0003 | t0001 | g0038 | AFR | GWD | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
HG02897 | hp2 | a0001 | c0001 | t0001 | g0229 | AFR | GWD | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
HG02922 | hp1 | a0003 | c0003 | t0001 | g0297 | AFR | ESN | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
HG02922 | hp2 | a0001 | c0001 | t0001 | g0023 | AFR | ESN | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
HG02965 | hp1 | a0002 | c0002 | t0001 | g0146 | AFR | ESN | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
HG02965 | hp2 | a0009 | c0012 | t0001 | g0286 | AFR | ESN | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
HG02976 | hp1 | a0001 | c0001 | t0001 | g0181 | AFR | ESN | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
HG02976 | hp2 | a0002 | c0006 | t0001 | g0136 | AFR | ESN | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
HG03017 | hp1 | a0002 | c0002 | t0002 | g0002 | SAS | PJL | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
HG03017 | hp2 | a0001 | c0001 | t0001 | g0107 | SAS | PJL | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
HG03041 | hp1 | a0002 | c0002 | t0001 | g0237 | AFR | GWD | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
HG03041 | hp2 | a0001 | c0001 | t0001 | g0021 | AFR | GWD | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
HG03098 | hp1 | a0005 | c0009 | t0001 | g0154 | AFR | MSL | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
HG03098 | hp2 | a0002 | c0002 | t0001 | g0233 | AFR | MSL | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
HG03130 | hp1 | a0002 | c0006 | t0001 | g0140 | AFR | ESN | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
HG03130 | hp2 | a0002 | c0002 | t0001 | g0239 | AFR | ESN | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
HG03139 | hp1 | a0002 | c0006 | t0001 | g0139 | AFR | ESN | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
HG03139 | hp2 | a0002 | c0005 | t0001 | g0034 | AFR | ESN | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
HG03195 | hp1 | a0001 | c0001 | t0001 | g0115 | AFR | ESN | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
HG03195 | hp2 | a0002 | c0005 | t0001 | g0310 | AFR | ESN | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
HG03209 | hp1 | a0002 | c0002 | t0001 | g0243 | AFR | MSL | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
HG03209 | hp2 | a0001 | c0001 | t0001 | g0226 | AFR | MSL | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
HG03225 | hp1 | a0001 | c0001 | t0001 | g0196 | AFR | MSL | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
HG03225 | hp2 | a0008 | c0013 | t0001 | g0294 | AFR | MSL | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
HG03239 | hp1 | a0001 | c0001 | t0001 | g0177 | SAS | PJL | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
HG03239 | hp2 | a0003 | c0003 | t0001 | g0293 | SAS | PJL | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
HG03453 | hp1 | a0002 | c0006 | t0001 | g0141 | AFR | MSL | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
HG03453 | hp2 | a0002 | c0005 | t0001 | g0232 | AFR | MSL | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
HG03486 | hp1 | a0002 | c0006 | t0001 | g0137 | AFR | MSL | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
HG03486 | hp2 | a0005 | c0007 | t0001 | g0272 | AFR | MSL | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
HG03491 | hp1 | a0014 | c0016 | t0002 | g0053 | SAS | PJL | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
HG03491 | hp2 | a0001 | c0001 | t0001 | g0029 | SAS | PJL | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
HG03492 | hp1 | a0001 | c0001 | t0001 | g0182 | SAS | PJL | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
HG03492 | hp2 | a0001 | c0001 | t0001 | g0192 | SAS | PJL | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
HG03516 | hp1 | a0001 | c0001 | t0001 | g0090 | AFR | ESN | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
HG03516 | hp2 | a0002 | c0005 | t0001 | g0245 | AFR | ESN | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
HG03540 | hp1 | a0001 | c0001 | t0001 | g0156 | AFR | GWD | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
HG03540 | hp2 | a0002 | c0002 | t0001 | g0148 | AFR | GWD | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
HG03579 | hp1 | a0002 | c0006 | t0001 | g0142 | AFR | MSL | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
HG03579 | hp2 | a0002 | c0005 | t0001 | g0306 | AFR | MSL | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
HG03654 | hp1 | a0001 | c0001 | t0001 | g0095 | SAS | PJL | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
HG03654 | hp2 | a0001 | c0001 | t0001 | g0254 | SAS | PJL | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
HG03669 | hp1 | a0001 | c0001 | t0001 | g0026 | SAS | PJL | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
HG03669 | hp2 | a0001 | c0001 | t0001 | g0005 | SAS | PJL | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
HG03688 | hp1 | a0001 | c0001 | t0001 | g0163 | SAS | STU | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
HG03688 | hp2 | a0003 | c0003 | t0001 | g0039 | SAS | STU | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
HG03710 | hp1 | a0003 | c0003 | t0001 | g0282 | SAS | PJL | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
HG03710 | hp2 | a0001 | c0001 | t0001 | g0187 | SAS | PJL | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
HG03831 | hp1 | a0003 | c0003 | t0001 | g0281 | SAS | BEB | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
HG03831 | hp2 | a0002 | c0002 | t0002 | g0007 | SAS | BEB | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
HG03834 | hp1 | a0001 | c0001 | t0001 | g0223 | SAS | BEB | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
HG03834 | hp2 | a0001 | c0001 | t0001 | g0108 | SAS | BEB | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
HG04115 | hp1 | a0001 | c0001 | t0001 | g0093 | SAS | STU | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
HG04115 | hp2 | a0001 | c0001 | t0001 | g0161 | SAS | STU | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
HG04199 | hp1 | a0001 | c0001 | t0001 | g0162 | SAS | STU | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
HG04199 | hp2 | a0001 | c0001 | t0001 | g0092 | SAS | STU | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
HG04204 | hp1 | a0001 | c0001 | t0001 | g0193 | SAS | STU | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
HG04204 | hp2 | a0002 | c0002 | t0002 | g0054 | SAS | STU | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
HG04228 | hp1 | a0001 | c0001 | t0001 | g0101 | SAS | STU | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
HG04228 | hp2 | a0002 | c0002 | t0002 | g0051 | SAS | STU | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
NA18522 | hp1 | a0011 | c0017 | t0001 | g0145 | AFR | YRI | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
NA18522 | hp2 | a0001 | c0001 | t0001 | g0008 | AFR | YRI | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
NA18612 | hp1 | a0001 | c0001 | t0001 | g0301 | EAS | CHB | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
NA18612 | hp2 | a0001 | c0001 | t0001 | g0116 | EAS | CHB | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
NA18906 | hp1 | a0001 | c0001 | t0003 | g0268 | AFR | YRI | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
NA18906 | hp2 | a0003 | c0003 | t0001 | g0287 | AFR | YRI | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
NA18942 | hp1 | a0001 | c0001 | t0003 | g0265 | EAS | JPT | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
NA18942 | hp2 | a0001 | c0001 | t0001 | g0179 | EAS | JPT | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
NA18943 | hp1 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
NA18943 | hp2 | a0004 | c0004 | t0003 | g0248 | EAS | JPT | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
NA18944 | hp1 | a0001 | c0001 | t0001 | g0028 | EAS | JPT | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
NA18944 | hp2 | a0004 | c0004 | t0003 | g0249 | EAS | JPT | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
NA18945 | hp1 | a0002 | c0002 | t0002 | g0065 | EAS | JPT | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
NA18945 | hp2 | a0001 | c0001 | t0001 | g0118 | EAS | JPT | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
NA18947 | hp1 | a0001 | c0001 | t0001 | g0089 | EAS | JPT | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
NA18947 | hp2 | a0001 | c0001 | t0001 | g0214 | EAS | JPT | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
NA18948 | hp1 | a0002 | c0002 | t0004 | g0079 | EAS | JPT | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
NA18948 | hp2 | a0001 | c0001 | t0001 | g0202 | EAS | JPT | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
NA18949 | hp1 | a0002 | c0002 | t0002 | g0073 | EAS | JPT | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
NA18949 | hp2 | a0001 | c0001 | t0001 | g0164 | EAS | JPT | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
NA18950 | hp1 | a0001 | c0001 | t0001 | g0124 | EAS | JPT | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
NA18950 | hp2 | a0001 | c0001 | t0001 | g0131 | EAS | JPT | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
NA18952 | hp1 | a0001 | c0001 | t0001 | g0032 | EAS | JPT | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
NA18952 | hp2 | a0002 | c0002 | t0002 | g0074 | EAS | JPT | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
NA18953 | hp1 | a0001 | c0001 | t0003 | g0256 | EAS | JPT | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
NA18953 | hp2 | a0002 | c0002 | t0002 | g0078 | EAS | JPT | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
NA18954 | hp1 | a0001 | c0001 | t0001 | g0024 | EAS | JPT | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
NA18954 | hp2 | a0001 | c0001 | t0001 | g0215 | EAS | JPT | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
NA18957 | hp1 | a0001 | c0001 | t0001 | g0221 | EAS | JPT | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
NA18957 | hp2 | a0001 | c0001 | t0001 | g0212 | EAS | JPT | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
NA18962 | hp1 | a0004 | c0004 | t0003 | g0010 | EAS | JPT | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
NA18962 | hp2 | a0001 | c0001 | t0001 | g0029 | EAS | JPT | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
NA18963 | hp1 | a0002 | c0002 | t0002 | g0048 | EAS | JPT | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
NA18963 | hp2 | a0016 | c0014 | t0003 | g0258 | EAS | JPT | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
NA18964 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
NA18964 | hp2 | a0002 | c0002 | t0002 | g0057 | EAS | JPT | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
NA18965 | hp1 | a0001 | c0001 | t0001 | g0022 | EAS | JPT | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
NA18965 | hp2 | a0001 | c0001 | t0003 | g0035 | EAS | JPT | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
NA18966 | hp1 | a0002 | c0002 | t0002 | g0069 | EAS | JPT | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
NA18966 | hp2 | a0001 | c0001 | t0003 | g0036 | EAS | JPT | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
NA18969 | hp1 | a0001 | c0001 | t0001 | g0176 | EAS | JPT | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
NA18969 | hp2 | a0007 | c0010 | t0001 | g0222 | EAS | JPT | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
NA18970 | hp1 | a0001 | c0011 | t0002 | g0070 | EAS | JPT | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
NA18970 | hp2 | a0001 | c0001 | t0001 | g0166 | EAS | JPT | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
NA18971 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
NA18971 | hp2 | a0001 | c0001 | t0001 | g0189 | EAS | JPT | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
NA18973 | hp1 | a0001 | c0001 | t0001 | g0167 | EAS | JPT | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
NA18973 | hp2 | a0001 | c0001 | t0001 | g0087 | EAS | JPT | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
NA18974 | hp1 | a0001 | c0001 | t0001 | g0190 | EAS | JPT | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
NA18974 | hp2 | a0002 | c0002 | t0002 | g0041 | EAS | JPT | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
NA18975 | hp1 | a0001 | c0001 | t0001 | g0121 | EAS | JPT | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
NA18975 | hp2 | a0002 | c0002 | t0002 | g0047 | EAS | JPT | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
NA18977 | hp1 | a0004 | c0004 | t0001 | g0264 | EAS | JPT | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
NA18977 | hp2 | a0001 | c0001 | t0001 | g0110 | EAS | JPT | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
NA18981 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
NA18981 | hp2 | a0002 | c0002 | t0002 | g0059 | EAS | JPT | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
NA18982 | hp1 | a0010 | c0018 | t0001 | g0173 | EAS | JPT | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
NA18982 | hp2 | a0001 | c0001 | t0001 | g0117 | EAS | JPT | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
NA18986 | hp1 | a0004 | c0004 | t0003 | g0257 | EAS | JPT | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
NA18986 | hp2 | a0001 | c0001 | t0001 | g0180 | EAS | JPT | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
NA18987 | hp1 | a0001 | c0001 | t0003 | g0253 | EAS | JPT | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
NA18987 | hp2 | a0001 | c0001 | t0001 | g0194 | EAS | JPT | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
NA18988 | hp1 | a0002 | c0002 | t0002 | g0015 | EAS | JPT | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
NA18988 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
NA18994 | hp1 | a0001 | c0001 | t0001 | g0218 | EAS | JPT | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
NA18994 | hp2 | a0004 | c0004 | t0003 | g0250 | EAS | JPT | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
NA18995 | hp1 | a0001 | c0001 | t0001 | g0200 | EAS | JPT | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
NA18995 | hp2 | a0001 | c0011 | t0002 | g0042 | EAS | JPT | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
NA18998 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
NA18998 | hp2 | a0007 | c0010 | t0001 | g0234 | EAS | JPT | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
NA19001 | hp1 | a0006 | c0008 | t0001 | g0174 | EAS | JPT | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
NA19001 | hp2 | a0001 | c0001 | t0001 | g0183 | EAS | JPT | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
NA19002 | hp1 | a0001 | c0001 | t0001 | g0305 | EAS | JPT | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
NA19002 | hp2 | a0001 | c0001 | t0003 | g0035 | EAS | JPT | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
NA19003 | hp1 | a0003 | c0003 | t0001 | g0283 | EAS | JPT | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
NA19003 | hp2 | a0001 | c0001 | t0001 | g0027 | EAS | JPT | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
NA19004 | hp1 | a0001 | c0001 | t0001 | g0024 | EAS | JPT | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
NA19004 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
NA19005 | hp1 | a0001 | c0001 | t0003 | g0247 | EAS | JPT | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
NA19005 | hp2 | a0002 | c0002 | t0002 | g0046 | EAS | JPT | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
NA19006 | hp1 | a0001 | c0001 | t0001 | g0126 | EAS | JPT | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
NA19006 | hp2 | a0015 | c0015 | t0002 | g0055 | EAS | JPT | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
NA19007 | hp1 | a0001 | c0001 | t0001 | g0201 | EAS | JPT | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
NA19007 | hp2 | a0004 | c0004 | t0003 | g0010 | EAS | JPT | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
NA19009 | hp1 | a0002 | c0002 | t0002 | g0063 | EAS | JPT | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
NA19009 | hp2 | a0004 | c0004 | t0003 | g0263 | EAS | JPT | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
NA19011 | hp1 | a0001 | c0001 | t0001 | g0120 | EAS | JPT | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
NA19011 | hp2 | a0002 | c0002 | t0002 | g0071 | EAS | JPT | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
NA19030 | hp1 | a0005 | c0007 | t0001 | g0271 | AFR | LWK | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
NA19030 | hp2 | a0002 | c0006 | t0001 | g0135 | AFR | LWK | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
NA19043 | hp1 | a0003 | c0003 | t0001 | g0277 | AFR | LWK | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
NA19043 | hp2 | a0002 | c0002 | t0001 | g0152 | AFR | LWK | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
NA19055 | hp1 | a0002 | c0002 | t0002 | g0077 | EAS | JPT | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
NA19055 | hp2 | a0001 | c0001 | t0003 | g0252 | EAS | JPT | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
NA19056 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
NA19056 | hp2 | a0004 | c0004 | t0003 | g0260 | EAS | JPT | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
NA19057 | hp1 | a0001 | c0001 | t0001 | g0224 | EAS | JPT | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
NA19057 | hp2 | a0001 | c0001 | t0001 | g0025 | EAS | JPT | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
NA19060 | hp1 | a0001 | c0001 | t0001 | g0028 | EAS | JPT | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
NA19060 | hp2 | a0001 | c0001 | t0001 | g0018 | EAS | JPT | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
NA19062 | hp1 | a0002 | c0002 | t0002 | g0013 | EAS | JPT | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
NA19062 | hp2 | a0001 | c0001 | t0001 | g0033 | EAS | JPT | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
NA19063 | hp1 | a0001 | c0001 | t0001 | g0205 | EAS | JPT | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
NA19063 | hp2 | a0004 | c0004 | t0003 | g0259 | EAS | JPT | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
NA19065 | hp1 | a0001 | c0001 | t0001 | g0027 | EAS | JPT | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
NA19065 | hp2 | a0002 | c0002 | t0002 | g0067 | EAS | JPT | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
NA19066 | hp1 | a0003 | c0003 | t0001 | g0295 | EAS | JPT | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
NA19066 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
NA19070 | hp1 | a0002 | c0002 | t0002 | g0083 | EAS | JPT | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
NA19070 | hp2 | a0002 | c0002 | t0002 | g0015 | EAS | JPT | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
NA19075 | hp1 | a0004 | c0004 | t0003 | g0261 | EAS | JPT | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
NA19075 | hp2 | a0001 | c0001 | t0001 | g0022 | EAS | JPT | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
NA19077 | hp1 | a0001 | c0001 | t0001 | g0155 | EAS | JPT | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
NA19077 | hp2 | a0001 | c0001 | t0003 | g0036 | EAS | JPT | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
NA19080 | hp1 | a0004 | c0004 | t0003 | g0010 | EAS | JPT | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
NA19080 | hp2 | a0001 | c0001 | t0001 | g0123 | EAS | JPT | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
NA19084 | hp1 | a0001 | c0001 | t0003 | g0006 | EAS | JPT | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
NA19084 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
NA19085 | hp1 | a0007 | c0010 | t0001 | g0188 | EAS | JPT | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
NA19085 | hp2 | a0002 | c0002 | t0002 | g0013 | EAS | JPT | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
NA19090 | hp1 | a0002 | c0002 | t0002 | g0044 | EAS | JPT | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
NA19090 | hp2 | a0004 | c0004 | t0003 | g0262 | EAS | JPT | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
NA19240 | hp1 | a0002 | c0005 | t0001 | g0040 | AFR | YRI | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
NA19240 | hp2 | a0001 | c0001 | t0001 | g0178 | AFR | YRI | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
NA20129 | hp1 | a0005 | c0009 | t0001 | g0020 | AFR | ASW | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
NA20129 | hp2 | a0001 | c0001 | t0001 | g0104 | AFR | ASW | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
NA20805 | hp1 | a0001 | c0001 | t0003 | g0006 | EUR | TSI | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
NA20805 | hp2 | a0001 | c0001 | t0001 | g0199 | EUR | TSI | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
NA20905 | hp1 | a0001 | c0001 | t0001 | g0085 | SAS | GIH | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
NA20905 | hp2 | a0001 | c0001 | t0001 | g0009 | SAS | GIH | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
HG01123 | hp1 | a0001 | c0001 | t0001 | g0031 | AMR | CLM | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
HG01123 | hp2 | a0001 | c0001 | t0003 | g0251 | AMR | CLM | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
HG02109 | hp1 | a0001 | c0001 | t0001 | g0217 | AFR | ACB | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
HG02109 | hp2 | a0005 | c0007 | t0001 | g0274 | AFR | ACB | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
HG02486 | hp1 | a0003 | c0003 | t0001 | g0011 | AFR | ACB | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
HG02486 | hp2 | a0002 | c0002 | t0001 | g0133 | AFR | ACB | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
HG02559 | hp1 | a0002 | c0006 | t0001 | g0127 | AFR | ACB | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
HG02559 | hp2 | a0002 | c0005 | t0001 | g0309 | AFR | ACB | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
HG03471 | hp1 | a0001 | c0001 | t0001 | g0300 | AFR | MSL | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
HG03471 | hp2 | a0005 | c0007 | t0001 | g0037 | AFR | MSL | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
NA18955 | hp1 | a0001 | c0001 | t0001 | g0159 | EAS | JPT | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
NA18955 | hp2 | a0002 | c0002 | t0002 | g0049 | EAS | JPT | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
NA20300 | hp1 | a0002 | c0006 | t0001 | g0132 | AFR | USA | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
NA20300 | hp2 | a0002 | c0002 | t0002 | g0062 | AFR | USA | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
NA21309 | hp1 | a0002 | c0002 | t0001 | g0175 | AFR | LWK | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
NA21309 | hp2 | a0001 | c0001 | t0001 | g0157 | AFR | LWK | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
homoSapiens_chm13v2 | hp1 | a0003 | c0003 | t0001 | g0291 | REF | REF | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
homoSapiens_grch38 | hp1 | a0001 | c0001 | t0001 | g0001 | REF | REF | GFM2_chr5_74716206_74772117 | GFM2 | chr5 | 74716206 | 74772117 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr5:74721674
|
C | T | 4 | a0003a0008a0009others(1): Show | 36 | HG00140.hp1 HG00280.hp2 HG00642.hp2 others(33): Show |
missense_variant | MODERATE | c.2321G>A | p.Arg774Gln | GFM2 | ENSG00000164347.18 | transcript | ENST00000296805.8 | protein_coding | 21/21 | 2525/2993 | 2321/2340 | 774/779 | chr5 | 74721674 | ||
chr5:74721765
|
G | C | 2 | a0006a0010 | 5 | HG00438.hp2 HG00735.hp2 HG02293.hp1 others(2): Show |
missense_variant | MODERATE | c.2230C>G | p.Arg744Gly | GFM2 | ENSG00000164347.18 | transcript | ENST00000296805.8 | protein_coding | 21/21 | 2434/2993 | 2230/2340 | 744/779 | chr5 | 74721765 | ||
chr5:74721782
|
C | T | 1 | a0016 | 1 | NA18963.hp2 | missense_variant&splice_region_variant | MODERATE | c.2213G>A | p.Gly738Asp | GFM2 | ENSG00000164347.18 | transcript | ENST00000296805.8 | protein_coding | 21/21 | 2417/2993 | 2213/2340 | 738/779 | chr5 | 74721782 | ||
chr5:74725968
|
T | C | 1 | a0011 | 1 | NA18522.hp1 | missense_variant | MODERATE | c.1885A>G | p.Asn629Asp | GFM2 | ENSG00000164347.18 | transcript | ENST00000296805.8 | protein_coding | 18/21 | 2089/2993 | 1885/2340 | 629/779 | chr5 | 74725968 | ||
chr5:74725973
|
A | G | 1 | a0008 | 2 | HG01243.hp2 HG03225.hp2 |
missense_variant | MODERATE | c.1880T>C | p.Ile627Thr | GFM2 | ENSG00000164347.18 | transcript | ENST00000296805.8 | protein_coding | 18/21 | 2084/2993 | 1880/2340 | 627/779 | chr5 | 74725973 | ||
chr5:74726021
|
TACTCAA | T | 10 | a0002a0003a0005others(7): Show | 151 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(148): Show |
disruptive_inframe_deletion | MODERATE | c.1826_1831delTTGAGT | p.Phe609_Glu610del | GFM2 | ENSG00000164347.18 | transcript | ENST00000296805.8 | protein_coding | 18/21 | 2035/2993 | 1826/2340 | 609/779 | chr5 | 74726021 | ||
chr5:74726093
|
T | G | 1 | a0013 | 1 | HG01952.hp1 | missense_variant | MODERATE | c.1760A>C | p.His587Pro | GFM2 | ENSG00000164347.18 | transcript | ENST00000296805.8 | protein_coding | 18/21 | 1964/2993 | 1760/2340 | 587/779 | chr5 | 74726093 | ||
chr5:74738526
|
A | G | 1 | a0016 | 1 | NA18963.hp2 | missense_variant | MODERATE | c.1196T>C | p.Ile399Thr | GFM2 | ENSG00000164347.18 | transcript | ENST00000296805.8 | protein_coding | 13/21 | 1400/2993 | 1196/2340 | 399/779 | chr5 | 74738526 | ||
chr5:74738620
|
A | G | 1 | a0014 | 1 | HG03491.hp1 | missense_variant | MODERATE | c.1102T>C | p.Cys368Arg | GFM2 | ENSG00000164347.18 | transcript | ENST00000296805.8 | protein_coding | 13/21 | 1306/2993 | 1102/2340 | 368/779 | chr5 | 74738620 | ||
chr5:74738628
|
T | C | 1 | a0007 | 3 | NA18969.hp2 NA18998.hp2 NA19085.hp1 |
missense_variant | MODERATE | c.1094A>G | p.Asp365Gly | GFM2 | ENSG00000164347.18 | transcript | ENST00000296805.8 | protein_coding | 13/21 | 1298/2993 | 1094/2340 | 365/779 | chr5 | 74738628 | ||
chr5:74741561
|
T | A | 2 | a0003a0008 | 33 | HG00140.hp1 HG00280.hp2 HG00738.hp2 others(30): Show |
missense_variant | MODERATE | c.898A>T | p.Ser300Cys | GFM2 | ENSG00000164347.18 | transcript | ENST00000296805.8 | protein_coding | 11/21 | 1102/2993 | 898/2340 | 300/779 | chr5 | 74741561 | ||
chr5:74745683
|
C | T | 1 | a0015 | 1 | NA19006.hp2 | missense_variant | MODERATE | c.844G>A | p.Glu282Lys | GFM2 | ENSG00000164347.18 | transcript | ENST00000296805.8 | protein_coding | 10/21 | 1048/2993 | 844/2340 | 282/779 | chr5 | 74745683 | ||
chr5:74759384
|
T | C | 4 | a0003a0005a0008others(1): Show | 46 | HG00140.hp1 HG00280.hp2 HG00642.hp2 others(43): Show |
missense_variant | MODERATE | c.191A>G | p.Asn64Ser | GFM2 | ENSG00000164347.18 | transcript | ENST00000296805.8 | protein_coding | 4/21 | 395/2993 | 191/2340 | 64/779 | chr5 | 74759384 | ||
chr5:74759397
|
G | T | 2 | a0004a0016 | 14 | NA18943.hp2 NA18944.hp2 NA18962.hp1 others(11): Show |
missense_variant | MODERATE | c.178C>A | p.His60Asn | GFM2 | ENSG00000164347.18 | transcript | ENST00000296805.8 | protein_coding | 4/21 | 382/2993 | 178/2340 | 60/779 | chr5 | 74759397 | ||
chr5:74763700
|
T | C | 1 | a0017 | 1 | HG01978.hp1 | missense_variant | MODERATE | c.43A>G | p.Ile15Val | GFM2 | ENSG00000164347.18 | transcript | ENST00000296805.8 | protein_coding | 2/21 | 247/2993 | 43/2340 | 15/779 | chr5 | 74763700 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr5:74726038
|
A | G | 1 | a0001c0020 | 1 | HG02083.hp2 | synonymous_variant | LOW | c.1815T>C | p.Pro605Pro | GFM2 | ENSG00000164347.18 | transcript | ENST00000296805.8 | protein_coding | 18/21 | 2019/2993 | 1815/2340 | 605/779 | chr5 | 74726038 | ||
chr5:74741544
|
C | T | 2 | a0002c0006a0012c0019 | 12 | HG02559.hp1 HG02615.hp2 HG02723.hp2 others(9): Show |
synonymous_variant | LOW | c.915G>A | p.Leu305Leu | GFM2 | ENSG00000164347.18 | transcript | ENST00000296805.8 | protein_coding | 11/21 | 1119/2993 | 915/2340 | 305/779 | chr5 | 74741544 | ||
chr5:74750639
|
C | T | 8 | a0001c0011a0002c0002a0005c0009others(5): Show | 87 | HG00099.hp2 HG00408.hp2 HG00438.hp2 others(84): Show |
synonymous_variant | LOW | c.459G>A | p.Glu153Glu | GFM2 | ENSG00000164347.18 | transcript | ENST00000296805.8 | protein_coding | 7/21 | 663/2993 | 459/2340 | 153/779 | chr5 | 74750639 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr5:74721255
|
CTG | C | 4 | a0001c0001t0003a0004c0004t0003a0016c0014t0003others(1): Show | 33 | HG00673.hp1 HG00741.hp1 HG01123.hp2 others(30): Show |
3_prime_UTR_variant | MODIFIER | c.*398_*399delCA | GFM2 | ENSG00000164347.18 | transcript | ENST00000296805.8 | protein_coding | 21/21 | 398 | chr5 | 74721255 | |||||
chr5:74721282
|
G | A | 1 | a0002c0002t0004 | 1 | NA18948.hp1 | 3_prime_UTR_variant | MODIFIER | c.*373C>T | GFM2 | ENSG00000164347.18 | transcript | ENST00000296805.8 | protein_coding | 21/21 | 373 | chr5 | 74721282 | |||||
chr5:74767056
|
C | T | 5 | a0001c0011t0002a0002c0002t0002a0002c0002t0004others(2): Show | 57 | HG00099.hp2 HG00408.hp2 HG00558.hp1 others(54): Show |
5_prime_UTR_variant | MODIFIER | c.-143G>A | GFM2 | ENSG00000164347.18 | transcript | ENST00000296805.8 | protein_coding | 1/21 | 3314 | chr5 | 74767056 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr5:74721963
|
G | A | 1 | a0001c0001t0001g0207 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.2212-180C>T | GFM2 | ENSG00000164347.18 | transcript | ENST00000296805.8 | protein_coding | 20/20 | chr5 | 74721963 | ||||||
chr5:74721983
|
T | C | 6 | a0005c0007t0001g0037a0005c0007t0001g0270a0005c0007t0001g0271others(3): Show | 7 | HG00733.hp2 HG01243.hp1 HG02109.hp2 others(4): Show |
intron_variant | MODIFIER | c.2212-200A>G | GFM2 | ENSG00000164347.18 | transcript | ENST00000296805.8 | protein_coding | 20/20 | chr5 | 74721983 | ||||||
chr5:74722252
|
A | AAACTT | 3 | a0001c0001t0001g0026a0001c0001t0001g0198a0001c0001t0001g0227 | 4 | HG00323.hp1 HG02683.hp1 HG02738.hp2 others(1): Show |
intron_variant | MODIFIER | c.2211+122_2211+126d others(7): Show |
GFM2 | ENSG00000164347.18 | transcript | ENST00000296805.8 | protein_coding | 20/20 | chr5 | 74722252 | ||||||
chr5:74722344
|
G | A | 1 | a0001c0001t0001g0215 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.2211+35C>T | GFM2 | ENSG00000164347.18 | transcript | ENST00000296805.8 | protein_coding | 20/20 | chr5 | 74722344 | ||||||
chr5:74722853
|
A | G | 1 | a0001c0001t0001g0113 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.2029-292T>C | GFM2 | ENSG00000164347.18 | transcript | ENST00000296805.8 | protein_coding | 19/20 | chr5 | 74722853 | ||||||
chr5:74722949
|
A | C | 35 | a0003c0003t0001g0011a0003c0003t0001g0012a0003c0003t0001g0038others(32): Show | 42 | HG00140.hp1 HG00280.hp2 HG00642.hp2 others(39): Show |
intron_variant | MODIFIER | c.2029-388T>G | GFM2 | ENSG00000164347.18 | transcript | ENST00000296805.8 | protein_coding | 19/20 | chr5 | 74722949 | ||||||
chr5:74723035
|
T | C | 1 | a0001c0001t0001g0220 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.2029-474A>G | GFM2 | ENSG00000164347.18 | transcript | ENST00000296805.8 | protein_coding | 19/20 | chr5 | 74723035 | ||||||
chr5:74723137
|
A | G | 1 | a0001c0001t0001g0201 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.2029-576T>C | GFM2 | ENSG00000164347.18 | transcript | ENST00000296805.8 | protein_coding | 19/20 | chr5 | 74723137 | ||||||
chr5:74723160
|
C | T | 1 | a0007c0010t0001g0234 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.2029-599G>A | GFM2 | ENSG00000164347.18 | transcript | ENST00000296805.8 | protein_coding | 19/20 | chr5 | 74723160 | ||||||
chr5:74723377
|
A | G | 2 | a0002c0005t0001g0231a0002c0005t0001g0232 | 2 | HG01891.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.2029-816T>C | GFM2 | ENSG00000164347.18 | transcript | ENST00000296805.8 | protein_coding | 19/20 | chr5 | 74723377 | ||||||
chr5:74723781
|
C | T | 4 | a0006c0008t0001g0134a0006c0008t0001g0171a0006c0008t0001g0172others(1): Show | 4 | HG00438.hp2 HG00735.hp2 HG02293.hp1 others(1): Show |
intron_variant | MODIFIER | c.2029-1220G>A | GFM2 | ENSG00000164347.18 | transcript | ENST00000296805.8 | protein_coding | 19/20 | chr5 | 74723781 | ||||||
chr5:74724204
|
C | T | 73 | a0002c0002t0001g0019a0002c0002t0001g0133a0002c0002t0001g0146others(70): Show | 84 | HG00099.hp2 HG00408.hp2 HG00438.hp2 others(81): Show |
intron_variant | MODIFIER | c.2028+1436G>A | GFM2 | ENSG00000164347.18 | transcript | ENST00000296805.8 | protein_coding | 19/20 | chr5 | 74724204 | ||||||
chr5:74724394
|
T | C | 2 | a0001c0001t0003g0035a0001c0001t0003g0253 | 3 | NA18965.hp2 NA18987.hp1 NA19002.hp2 |
intron_variant | MODIFIER | c.2028+1246A>G | GFM2 | ENSG00000164347.18 | transcript | ENST00000296805.8 | protein_coding | 19/20 | chr5 | 74724394 | ||||||
chr5:74724410
|
G | A | 9 | a0003c0003t0001g0012a0003c0003t0001g0275a0003c0003t0001g0276others(6): Show | 11 | HG00140.hp1 HG00280.hp2 HG00738.hp2 others(8): Show |
intron_variant | MODIFIER | c.2028+1230C>T | GFM2 | ENSG00000164347.18 | transcript | ENST00000296805.8 | protein_coding | 19/20 | chr5 | 74724410 | ||||||
chr5:74724473
|
T | TA | 20 | a0001c0001t0001g0194a0001c0001t0001g0198a0001c0001t0001g0227others(17): Show | 23 | HG01175.hp1 HG01175.hp2 HG02145.hp1 others(20): Show |
intron_variant | MODIFIER | c.2028+1166dupT | GFM2 | ENSG00000164347.18 | transcript | ENST00000296805.8 | protein_coding | 19/20 | chr5 | 74724473 | ||||||
chr5:74724473
|
TA | T | 58 | a0001c0001t0001g0212a0001c0001t0003g0253a0002c0002t0002g0013others(55): Show | 67 | HG00140.hp1 HG00280.hp2 HG00642.hp2 others(64): Show |
intron_variant | MODIFIER | c.2028+1166delT | GFM2 | ENSG00000164347.18 | transcript | ENST00000296805.8 | protein_coding | 19/20 | chr5 | 74724473 | ||||||
chr5:74724678
|
T | G | 1 | a0005c0007t0001g0273 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.2028+962A>C | GFM2 | ENSG00000164347.18 | transcript | ENST00000296805.8 | protein_coding | 19/20 | chr5 | 74724678 | ||||||
chr5:74724720
|
C | T | 1 | a0002c0006t0001g0135 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.2028+920G>A | GFM2 | ENSG00000164347.18 | transcript | ENST00000296805.8 | protein_coding | 19/20 | chr5 | 74724720 | ||||||
chr5:74724915
|
G | A | 1 | a0002c0002t0001g0302 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.2028+725C>T | GFM2 | ENSG00000164347.18 | transcript | ENST00000296805.8 | protein_coding | 19/20 | chr5 | 74724915 | ||||||
chr5:74724987
|
C | G | 4 | a0001c0001t0001g0003a0001c0001t0001g0094a0001c0001t0001g0100others(1): Show | 8 | HG01928.hp1 HG01943.hp2 HG01975.hp1 others(5): Show |
intron_variant | MODIFIER | c.2028+653G>C | GFM2 | ENSG00000164347.18 | transcript | ENST00000296805.8 | protein_coding | 19/20 | chr5 | 74724987 | ||||||
chr5:74725310
|
G | A | 2 | a0002c0005t0001g0231a0002c0005t0001g0232 | 2 | HG01891.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.2028+330C>T | GFM2 | ENSG00000164347.18 | transcript | ENST00000296805.8 | protein_coding | 19/20 | chr5 | 74725310 | ||||||
chr5:74725376
|
T | C | 4 | a0002c0002t0002g0051a0002c0002t0002g0080a0002c0002t0002g0081others(1): Show | 4 | HG00099.hp2 HG01069.hp2 HG01071.hp2 others(1): Show |
intron_variant | MODIFIER | c.2028+264A>G | GFM2 | ENSG00000164347.18 | transcript | ENST00000296805.8 | protein_coding | 19/20 | chr5 | 74725376 | ||||||
chr5:74725499
|
T | C | 1 | a0002c0002t0002g0068 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.2028+141A>G | GFM2 | ENSG00000164347.18 | transcript | ENST00000296805.8 | protein_coding | 19/20 | chr5 | 74725499 | ||||||
chr5:74725930
|
G | A | 2 | a0002c0005t0001g0231a0002c0005t0001g0232 | 2 | HG01891.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.1912+11C>T | GFM2 | ENSG00000164347.18 | transcript | ENST00000296805.8 | protein_coding | 18/20 | chr5 | 74725930 | ||||||
chr5:74726280
|
CAGAG | C | 35 | a0003c0003t0001g0011a0003c0003t0001g0012a0003c0003t0001g0038others(32): Show | 42 | HG00140.hp1 HG00280.hp2 HG00642.hp2 others(39): Show |
intron_variant | MODIFIER | c.1727-158_1727-155d others(6): Show |
GFM2 | ENSG00000164347.18 | transcript | ENST00000296805.8 | protein_coding | 17/20 | chr5 | 74726280 | ||||||
chr5:74726313
|
T | C | 2 | a0003c0003t0001g0281a0003c0003t0001g0282 | 2 | HG03710.hp1 HG03831.hp1 |
intron_variant | MODIFIER | c.1727-187A>G | GFM2 | ENSG00000164347.18 | transcript | ENST00000296805.8 | protein_coding | 17/20 | chr5 | 74726313 | ||||||
chr5:74726525
|
G | T | 48 | a0001c0011t0002g0042a0001c0011t0002g0070a0002c0002t0002g0002others(45): Show | 57 | HG00099.hp2 HG00408.hp2 HG00558.hp1 others(54): Show |
intron_variant | MODIFIER | c.1727-399C>A | GFM2 | ENSG00000164347.18 | transcript | ENST00000296805.8 | protein_coding | 17/20 | chr5 | 74726525 | ||||||
chr5:74726644
|
T | C | 1 | a0002c0002t0002g0075 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.1727-518A>G | GFM2 | ENSG00000164347.18 | transcript | ENST00000296805.8 | protein_coding | 17/20 | chr5 | 74726644 | ||||||
chr5:74726807
|
G | C | 1 | a0002c0005t0001g0034 | 2 | HG02451.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.1727-681C>G | GFM2 | ENSG00000164347.18 | transcript | ENST00000296805.8 | protein_coding | 17/20 | chr5 | 74726807 | ||||||
chr5:74726841
|
C | T | 14 | a0002c0002t0001g0019a0002c0002t0001g0133a0002c0002t0001g0146others(11): Show | 16 | HG00741.hp2 HG01106.hp1 HG01167.hp1 others(13): Show |
intron_variant | MODIFIER | c.1727-715G>A | GFM2 | ENSG00000164347.18 | transcript | ENST00000296805.8 | protein_coding | 17/20 | chr5 | 74726841 | ||||||
chr5:74727216
|
C | T | 130 | a0002c0002t0001g0019a0002c0002t0001g0133a0002c0002t0001g0146others(127): Show | 150 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(147): Show |
intron_variant | MODIFIER | c.1727-1090G>A | GFM2 | ENSG00000164347.18 | transcript | ENST00000296805.8 | protein_coding | 17/20 | chr5 | 74727216 | ||||||
chr5:74727304
|
A | G | 1 | a0001c0001t0001g0199 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.1727-1178T>C | GFM2 | ENSG00000164347.18 | transcript | ENST00000296805.8 | protein_coding | 17/20 | chr5 | 74727304 | ||||||
chr5:74727655
|
A | C | 2 | a0001c0011t0002g0042a0001c0011t0002g0070 | 2 | NA18970.hp1 NA18995.hp2 |
intron_variant | MODIFIER | c.1727-1529T>G | GFM2 | ENSG00000164347.18 | transcript | ENST00000296805.8 | protein_coding | 17/20 | chr5 | 74727655 | ||||||
chr5:74727815
|
T | C | 35 | a0003c0003t0001g0011a0003c0003t0001g0012a0003c0003t0001g0038others(32): Show | 42 | HG00140.hp1 HG00280.hp2 HG00642.hp2 others(39): Show |
intron_variant | MODIFIER | c.1727-1689A>G | GFM2 | ENSG00000164347.18 | transcript | ENST00000296805.8 | protein_coding | 17/20 | chr5 | 74727815 | ||||||
chr5:74727858
|
A | G | 4 | a0001c0001t0001g0030a0001c0001t0001g0170a0001c0001t0001g0204others(1): Show | 5 | HG00408.hp1 HG02040.hp1 HG02132.hp1 others(2): Show |
intron_variant | MODIFIER | c.1727-1732T>C | GFM2 | ENSG00000164347.18 | transcript | ENST00000296805.8 | protein_coding | 17/20 | chr5 | 74727858 | ||||||
chr5:74727975
|
G | A | 3 | a0001c0001t0001g0119a0001c0001t0001g0123a0001c0001t0001g0126 | 3 | HG02165.hp2 NA19006.hp1 NA19080.hp2 |
intron_variant | MODIFIER | c.1727-1849C>T | GFM2 | ENSG00000164347.18 | transcript | ENST00000296805.8 | protein_coding | 17/20 | chr5 | 74727975 | ||||||
chr5:74727994
|
T | A | 4 | a0001c0001t0001g0089a0001c0001t0001g0110a0001c0001t0001g0116others(1): Show | 4 | NA18612.hp2 NA18947.hp1 NA18950.hp1 others(1): Show |
intron_variant | MODIFIER | c.1727-1868A>T | GFM2 | ENSG00000164347.18 | transcript | ENST00000296805.8 | protein_coding | 17/20 | chr5 | 74727994 | ||||||
chr5:74728057
|
G | A | 1 | a0002c0002t0001g0019 | 2 | HG00741.hp2 HG01106.hp1 |
intron_variant | MODIFIER | c.1727-1931C>T | GFM2 | ENSG00000164347.18 | transcript | ENST00000296805.8 | protein_coding | 17/20 | chr5 | 74728057 | ||||||
chr5:74728115
|
C | T | 1 | a0004c0004t0003g0260 | 1 | NA19056.hp2 | intron_variant | MODIFIER | c.1727-1989G>A | GFM2 | ENSG00000164347.18 | transcript | ENST00000296805.8 | protein_coding | 17/20 | chr5 | 74728115 | ||||||
chr5:74728209
|
T | C | 1 | a0001c0001t0001g0102 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.1726+2051A>G | GFM2 | ENSG00000164347.18 | transcript | ENST00000296805.8 | protein_coding | 17/20 | chr5 | 74728209 | ||||||
chr5:74728349
|
G | GT | 48 | a0001c0011t0002g0042a0001c0011t0002g0070a0002c0002t0002g0002others(45): Show | 57 | HG00099.hp2 HG00408.hp2 HG00558.hp1 others(54): Show |
intron_variant | MODIFIER | c.1726+1910dupA | GFM2 | ENSG00000164347.18 | transcript | ENST00000296805.8 | protein_coding | 17/20 | chr5 | 74728349 | ||||||
chr5:74728395
|
A | T | 1 | a0002c0006t0001g0135 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1726+1865T>A | GFM2 | ENSG00000164347.18 | transcript | ENST00000296805.8 | protein_coding | 17/20 | chr5 | 74728395 | ||||||
chr5:74728591
|
A | C | 1 | a0002c0002t0001g0175 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1726+1669T>G | GFM2 | ENSG00000164347.18 | transcript | ENST00000296805.8 | protein_coding | 17/20 | chr5 | 74728591 | ||||||
chr5:74728748
|
C | CT | 74 | a0001c0001t0001g0016a0001c0001t0001g0086a0001c0001t0001g0087others(71): Show | 86 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(83): Show |
intron_variant | MODIFIER | c.1726+1511dupA | GFM2 | ENSG00000164347.18 | transcript | ENST00000296805.8 | protein_coding | 17/20 | chr5 | 74728748 | ||||||
chr5:74728748
|
C | CTT | 23 | a0001c0001t0001g0088a0001c0001t0001g0098a0001c0001t0001g0105others(20): Show | 23 | HG00621.hp2 HG01109.hp1 HG01258.hp2 others(20): Show |
intron_variant | MODIFIER | c.1726+1510_1726+151 others(6): Show |
GFM2 | ENSG00000164347.18 | transcript | ENST00000296805.8 | protein_coding | 17/20 | chr5 | 74728748 | ||||||
chr5:74728748
|
CT | C | 9 | a0001c0001t0001g0025a0001c0001t0001g0123a0001c0001t0001g0125others(6): Show | 10 | HG01943.hp2 HG02523.hp1 HG02735.hp2 others(7): Show |
intron_variant | MODIFIER | c.1726+1511delA | GFM2 | ENSG00000164347.18 | transcript | ENST00000296805.8 | protein_coding | 17/20 | chr5 | 74728748 | ||||||
chr5:74728748
|
CTT | C | 6 | a0002c0002t0001g0238a0002c0002t0001g0239a0002c0002t0001g0240others(3): Show | 6 | HG01884.hp2 HG02280.hp1 HG02647.hp1 others(3): Show |
intron_variant | MODIFIER | c.1726+1510_1726+151 others(6): Show |
GFM2 | ENSG00000164347.18 | transcript | ENST00000296805.8 | protein_coding | 17/20 | chr5 | 74728748 | ||||||
chr5:74728748
|
CTTTTTT | C | 7 | a0002c0005t0001g0034a0002c0005t0001g0040a0002c0005t0001g0244others(4): Show | 9 | HG02145.hp2 HG02451.hp2 HG02559.hp2 others(6): Show |
intron_variant | MODIFIER | c.1726+1506_1726+151 others(10): Show |
GFM2 | ENSG00000164347.18 | transcript | ENST00000296805.8 | protein_coding | 17/20 | chr5 | 74728748 | ||||||
chr5:74728748
|
CTTTTTTT others(2): Show |
C | 13 | a0001c0001t0001g0158a0001c0001t0001g0176a0001c0001t0001g0182others(10): Show | 13 | HG00735.hp1 HG02148.hp2 HG03225.hp1 others(10): Show |
intron_variant | MODIFIER | c.1726+1503_1726+151 others(13): Show |
GFM2 | ENSG00000164347.18 | transcript | ENST00000296805.8 | protein_coding | 17/20 | chr5 | 74728748 | ||||||
chr5:74728748
|
CTTTTTTT others(9): Show |
C | 12 | a0002c0006t0001g0127a0002c0006t0001g0132a0002c0006t0001g0135others(9): Show | 12 | HG02559.hp1 HG02615.hp2 HG02723.hp2 others(9): Show |
intron_variant | MODIFIER | c.1726+1496_1726+151 others(20): Show |
GFM2 | ENSG00000164347.18 | transcript | ENST00000296805.8 | protein_coding | 17/20 | chr5 | 74728748 | ||||||
chr5:74728759
|
T | C | 15 | a0001c0001t0001g0129a0001c0001t0001g0130a0001c0001t0001g0131others(12): Show | 17 | HG00621.hp1 HG02080.hp2 NA18943.hp2 others(14): Show |
intron_variant | MODIFIER | c.1726+1501A>G | GFM2 | ENSG00000164347.18 | transcript | ENST00000296805.8 | protein_coding | 17/20 | chr5 | 74728759 | ||||||
chr5:74728770
|
T | TTTTTTTG others(3): Show |
30 | a0003c0003t0001g0011a0003c0003t0001g0012a0003c0003t0001g0038others(27): Show | 37 | HG00140.hp1 HG00280.hp2 HG00733.hp2 others(34): Show |
intron_variant | MODIFIER | c.1726+1489_1726+149 others(14): Show |
GFM2 | ENSG00000164347.18 | transcript | ENST00000296805.8 | protein_coding | 17/20 | chr5 | 74728770 | ||||||
chr5:74728770
|
T | TTTTTTTT others(4): Show |
4 | a0003c0003t0001g0280a0003c0003t0001g0287a0003c0003t0001g0288others(1): Show | 4 | HG00642.hp2 HG01109.hp2 HG02148.hp1 others(1): Show |
intron_variant | MODIFIER | c.1726+1489_1726+149 others(15): Show |
GFM2 | ENSG00000164347.18 | transcript | ENST00000296805.8 | protein_coding | 17/20 | chr5 | 74728770 | ||||||
chr5:74728826
|
A | G | 1 | a0011c0017t0001g0145 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.1726+1434T>C | GFM2 | ENSG00000164347.18 | transcript | ENST00000296805.8 | protein_coding | 17/20 | chr5 | 74728826 | ||||||
chr5:74728973
|
C | G | 3 | a0002c0002t0001g0239a0002c0002t0001g0240a0002c0002t0001g0243 | 3 | HG02809.hp1 HG03130.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.1726+1287G>C | GFM2 | ENSG00000164347.18 | transcript | ENST00000296805.8 | protein_coding | 17/20 | chr5 | 74728973 | ||||||
chr5:74729044
|
A | G | 35 | a0003c0003t0001g0011a0003c0003t0001g0012a0003c0003t0001g0038others(32): Show | 42 | HG00140.hp1 HG00280.hp2 HG00642.hp2 others(39): Show |
intron_variant | MODIFIER | c.1726+1216T>C | GFM2 | ENSG00000164347.18 | transcript | ENST00000296805.8 | protein_coding | 17/20 | chr5 | 74729044 | ||||||
chr5:74729048
|
G | A | 70 | a0002c0002t0001g0019a0002c0002t0001g0133a0002c0002t0001g0146others(67): Show | 81 | HG00099.hp2 HG00408.hp2 HG00438.hp2 others(78): Show |
intron_variant | MODIFIER | c.1726+1212C>T | GFM2 | ENSG00000164347.18 | transcript | ENST00000296805.8 | protein_coding | 17/20 | chr5 | 74729048 | ||||||
chr5:74729110
|
T | C | 1 | a0005c0007t0001g0270 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.1726+1150A>G | GFM2 | ENSG00000164347.18 | transcript | ENST00000296805.8 | protein_coding | 17/20 | chr5 | 74729110 | ||||||
chr5:74729129
|
G | A | 3 | a0002c0002t0001g0175a0002c0002t0001g0233a0002c0002t0001g0237 | 3 | HG03041.hp1 HG03098.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.1726+1131C>T | GFM2 | ENSG00000164347.18 | transcript | ENST00000296805.8 | protein_coding | 17/20 | chr5 | 74729129 | ||||||
chr5:74729168
|
G | A | 1 | a0002c0002t0002g0045 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.1726+1092C>T | GFM2 | ENSG00000164347.18 | transcript | ENST00000296805.8 | protein_coding | 17/20 | chr5 | 74729168 | ||||||
chr5:74729236
|
T | G | 1 | a0001c0001t0001g0227 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.1726+1024A>C | GFM2 | ENSG00000164347.18 | transcript | ENST00000296805.8 | protein_coding | 17/20 | chr5 | 74729236 | ||||||
chr5:74729325
|
A | G | 35 | a0003c0003t0001g0011a0003c0003t0001g0012a0003c0003t0001g0038others(32): Show | 42 | HG00140.hp1 HG00280.hp2 HG00642.hp2 others(39): Show |
intron_variant | MODIFIER | c.1726+935T>C | GFM2 | ENSG00000164347.18 | transcript | ENST00000296805.8 | protein_coding | 17/20 | chr5 | 74729325 | ||||||
chr5:74729441
|
A | G | 132 | a0002c0002t0001g0019a0002c0002t0001g0133a0002c0002t0001g0146others(129): Show | 152 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(149): Show |
intron_variant | MODIFIER | c.1726+819T>C | GFM2 | ENSG00000164347.18 | transcript | ENST00000296805.8 | protein_coding | 17/20 | chr5 | 74729441 | ||||||
chr5:74729483
|
A | G | 1 | a0011c0017t0001g0145 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.1726+777T>C | GFM2 | ENSG00000164347.18 | transcript | ENST00000296805.8 | protein_coding | 17/20 | chr5 | 74729483 | ||||||
chr5:74729678
|
C | CT | 27 | a0002c0002t0001g0150a0002c0005t0001g0034a0002c0005t0001g0040others(24): Show | 29 | HG00438.hp2 HG00735.hp2 HG01167.hp1 others(26): Show |
intron_variant | MODIFIER | c.1726+581dupA | GFM2 | ENSG00000164347.18 | transcript | ENST00000296805.8 | protein_coding | 17/20 | chr5 | 74729678 | ||||||
chr5:74729678
|
C | CTT | 66 | a0002c0002t0001g0019a0002c0002t0001g0133a0002c0002t0001g0146others(63): Show | 77 | HG00099.hp2 HG00408.hp2 HG00558.hp1 others(74): Show |
intron_variant | MODIFIER | c.1726+580_1726+581d others(4): Show |
GFM2 | ENSG00000164347.18 | transcript | ENST00000296805.8 | protein_coding | 17/20 | chr5 | 74729678 | ||||||
chr5:74729678
|
CT | C | 8 | a0001c0001t0001g0107a0001c0001t0001g0191a0001c0001t0001g0225others(5): Show | 9 | HG01074.hp1 HG01167.hp2 HG01169.hp1 others(6): Show |
intron_variant | MODIFIER | c.1726+581delA | GFM2 | ENSG00000164347.18 | transcript | ENST00000296805.8 | protein_coding | 17/20 | chr5 | 74729678 | ||||||
chr5:74729819
|
C | G | 1 | a0001c0001t0001g0101 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.1726+441G>C | GFM2 | ENSG00000164347.18 | transcript | ENST00000296805.8 | protein_coding | 17/20 | chr5 | 74729819 | ||||||
chr5:74729893
|
T | C | 3 | a0002c0002t0001g0175a0002c0002t0001g0233a0002c0002t0001g0237 | 3 | HG03041.hp1 HG03098.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.1726+367A>G | GFM2 | ENSG00000164347.18 | transcript | ENST00000296805.8 | protein_coding | 17/20 | chr5 | 74729893 | ||||||
chr5:74730551
|
T | C | 6 | a0002c0002t0001g0238a0002c0002t0001g0239a0002c0002t0001g0240others(3): Show | 6 | HG01884.hp2 HG02280.hp1 HG02647.hp1 others(3): Show |
intron_variant | MODIFIER | c.1588-153A>G | GFM2 | ENSG00000164347.18 | transcript | ENST00000296805.8 | protein_coding | 16/20 | chr5 | 74730551 | ||||||
chr5:74730838
|
A | T | 1 | a0001c0001t0001g0193 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.1588-440T>A | GFM2 | ENSG00000164347.18 | transcript | ENST00000296805.8 | protein_coding | 16/20 | chr5 | 74730838 | ||||||
chr5:74730845
|
C | T | 12 | a0002c0006t0001g0127a0002c0006t0001g0132a0002c0006t0001g0135others(9): Show | 12 | HG02559.hp1 HG02615.hp2 HG02723.hp2 others(9): Show |
intron_variant | MODIFIER | c.1588-447G>A | GFM2 | ENSG00000164347.18 | transcript | ENST00000296805.8 | protein_coding | 16/20 | chr5 | 74730845 | ||||||
chr5:74730850
|
G | A | 1 | a0001c0001t0001g0169 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.1588-452C>T | GFM2 | ENSG00000164347.18 | transcript | ENST00000296805.8 | protein_coding | 16/20 | chr5 | 74730850 | ||||||
chr5:74731059
|
T | C | 58 | a0002c0005t0001g0034a0002c0005t0001g0040a0002c0005t0001g0231others(55): Show | 67 | HG00140.hp1 HG00280.hp2 HG00642.hp2 others(64): Show |
intron_variant | MODIFIER | c.1588-661A>G | GFM2 | ENSG00000164347.18 | transcript | ENST00000296805.8 | protein_coding | 16/20 | chr5 | 74731059 | ||||||
chr5:74731194
|
A | G | 1 | a0001c0001t0001g0114 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.1588-796T>C | GFM2 | ENSG00000164347.18 | transcript | ENST00000296805.8 | protein_coding | 16/20 | chr5 | 74731194 | ||||||
chr5:74731357
|
G | T | 1 | a0006c0008t0001g0172 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.1588-959C>A | GFM2 | ENSG00000164347.18 | transcript | ENST00000296805.8 | protein_coding | 16/20 | chr5 | 74731357 | ||||||
chr5:74731423
|
C | T | 1 | a0001c0001t0003g0266 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.1588-1025G>A | GFM2 | ENSG00000164347.18 | transcript | ENST00000296805.8 | protein_coding | 16/20 | chr5 | 74731423 | ||||||
chr5:74731611
|
T | G | 11 | a0002c0006t0001g0127a0002c0006t0001g0132a0002c0006t0001g0136others(8): Show | 11 | HG02559.hp1 HG02615.hp2 HG02723.hp2 others(8): Show |
intron_variant | MODIFIER | c.1588-1213A>C | GFM2 | ENSG00000164347.18 | transcript | ENST00000296805.8 | protein_coding | 16/20 | chr5 | 74731611 | ||||||
chr5:74731620
|
T | TA | 9 | a0002c0005t0001g0034a0002c0005t0001g0040a0002c0005t0001g0244others(6): Show | 11 | HG02145.hp2 HG02451.hp2 HG02559.hp2 others(8): Show |
intron_variant | MODIFIER | c.1588-1223dupT | GFM2 | ENSG00000164347.18 | transcript | ENST00000296805.8 | protein_coding | 16/20 | chr5 | 74731620 | ||||||
chr5:74731872
|
C | T | 1 | a0003c0003t0001g0287 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.1587+1150G>A | GFM2 | ENSG00000164347.18 | transcript | ENST00000296805.8 | protein_coding | 16/20 | chr5 | 74731872 | ||||||
chr5:74732128
|
A | AT | 21 | a0001c0001t0001g0008a0001c0001t0001g0092a0001c0001t0001g0097others(18): Show | 23 | HG01099.hp2 HG01168.hp2 HG01884.hp1 others(20): Show |
intron_variant | MODIFIER | c.1587+893dupA | GFM2 | ENSG00000164347.18 | transcript | ENST00000296805.8 | protein_coding | 16/20 | chr5 | 74732128 | ||||||
chr5:74732128
|
AT | A | 30 | a0001c0001t0001g0212a0001c0001t0003g0256a0002c0002t0002g0077others(27): Show | 36 | HG00140.hp1 HG00280.hp2 HG00642.hp2 others(33): Show |
intron_variant | MODIFIER | c.1587+893delA | GFM2 | ENSG00000164347.18 | transcript | ENST00000296805.8 | protein_coding | 16/20 | chr5 | 74732128 | ||||||
chr5:74732315
|
T | A | 1 | a0004c0004t0003g0262 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.1587+707A>T | GFM2 | ENSG00000164347.18 | transcript | ENST00000296805.8 | protein_coding | 16/20 | chr5 | 74732315 | ||||||
chr5:74732417
|
T | G | 1 | a0001c0001t0003g0268 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.1587+605A>C | GFM2 | ENSG00000164347.18 | transcript | ENST00000296805.8 | protein_coding | 16/20 | chr5 | 74732417 | ||||||
chr5:74732453
|
T | C | 1 | a0001c0001t0001g0223 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.1587+569A>G | GFM2 | ENSG00000164347.18 | transcript | ENST00000296805.8 | protein_coding | 16/20 | chr5 | 74732453 | ||||||
chr5:74732475
|
TAAAAAGA others(8): Show |
T | 1 | a0001c0001t0001g0191 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.1587+532_1587+546d others(17): Show |
GFM2 | ENSG00000164347.18 | transcript | ENST00000296805.8 | protein_coding | 16/20 | chr5 | 74732475 | ||||||
chr5:74732495
|
T | C | 1 | a0001c0001t0001g0191 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.1587+527A>G | GFM2 | ENSG00000164347.18 | transcript | ENST00000296805.8 | protein_coding | 16/20 | chr5 | 74732495 | ||||||
chr5:74732602
|
T | C | 6 | a0005c0007t0001g0037a0005c0007t0001g0270a0005c0007t0001g0271others(3): Show | 7 | HG00733.hp2 HG01243.hp1 HG02109.hp2 others(4): Show |
intron_variant | MODIFIER | c.1587+420A>G | GFM2 | ENSG00000164347.18 | transcript | ENST00000296805.8 | protein_coding | 16/20 | chr5 | 74732602 | ||||||
chr5:74732891
|
A | G | 1 | a0001c0001t0001g0199 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.1587+131T>C | GFM2 | ENSG00000164347.18 | transcript | ENST00000296805.8 | protein_coding | 16/20 | chr5 | 74732891 | ||||||
chr5:74732927
|
G | GAC | 32 | a0001c0001t0001g0027a0001c0001t0001g0028a0001c0001t0001g0031others(29): Show | 41 | HG00099.hp2 HG00558.hp1 HG00738.hp1 others(38): Show |
intron_variant | MODIFIER | c.1587+93_1587+94dup others(2): Show |
GFM2 | ENSG00000164347.18 | transcript | ENST00000296805.8 | protein_coding | 16/20 | chr5 | 74732927 | ||||||
chr5:74732927
|
G | GACAC | 25 | a0001c0001t0001g0189a0001c0001t0001g0201a0001c0001t0001g0202others(22): Show | 29 | HG00408.hp2 HG01257.hp2 HG01258.hp1 others(26): Show |
intron_variant | MODIFIER | c.1587+91_1587+94dup others(4): Show |
GFM2 | ENSG00000164347.18 | transcript | ENST00000296805.8 | protein_coding | 16/20 | chr5 | 74732927 | ||||||
chr5:74732927
|
G | GACACAC | 13 | a0001c0001t0001g0032a0001c0001t0001g0209a0001c0001t0001g0213others(10): Show | 14 | HG01346.hp1 HG01934.hp2 HG02015.hp1 others(11): Show |
intron_variant | MODIFIER | c.1587+89_1587+94dup others(6): Show |
GFM2 | ENSG00000164347.18 | transcript | ENST00000296805.8 | protein_coding | 16/20 | chr5 | 74732927 | ||||||
chr5:74732927
|
G | GACACACA others(3): Show |
1 | a0001c0001t0001g0033 | 2 | HG00673.hp2 NA19062.hp2 |
intron_variant | MODIFIER | c.1587+85_1587+94dup others(10): Show |
GFM2 | ENSG00000164347.18 | transcript | ENST00000296805.8 | protein_coding | 16/20 | chr5 | 74732927 | ||||||
chr5:74732927
|
GAC | G | 19 | a0001c0001t0001g0022a0001c0001t0001g0029a0001c0001t0001g0094others(16): Show | 21 | HG00558.hp2 HG01243.hp2 HG01261.hp1 others(18): Show |
intron_variant | MODIFIER | c.1587+93_1587+94del others(2): Show |
GFM2 | ENSG00000164347.18 | transcript | ENST00000296805.8 | protein_coding | 16/20 | chr5 | 74732927 | ||||||
chr5:74732927
|
GACAC | G | 65 | a0001c0001t0001g0005a0001c0001t0001g0008a0001c0001t0001g0021others(62): Show | 76 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(73): Show |
intron_variant | MODIFIER | c.1587+91_1587+94del others(4): Show |
GFM2 | ENSG00000164347.18 | transcript | ENST00000296805.8 | protein_coding | 16/20 | chr5 | 74732927 | ||||||
chr5:74732927
|
GACACAC | G | 65 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0017others(62): Show | 82 | HG00140.hp2 HG00621.hp2 HG00741.hp1 others(79): Show |
intron_variant | MODIFIER | c.1587+89_1587+94del others(6): Show |
GFM2 | ENSG00000164347.18 | transcript | ENST00000296805.8 | protein_coding | 16/20 | chr5 | 74732927 | ||||||
chr5:74732927
|
GACACACA others(1): Show |
G | 18 | a0001c0001t0001g0016a0001c0001t0001g0092a0001c0001t0001g0096others(15): Show | 21 | HG01081.hp2 HG01106.hp2 HG01258.hp2 others(18): Show |
intron_variant | MODIFIER | c.1587+87_1587+94del others(8): Show |
GFM2 | ENSG00000164347.18 | transcript | ENST00000296805.8 | protein_coding | 16/20 | chr5 | 74732927 | ||||||
chr5:74732927
|
GACACACA others(3): Show |
G | 22 | a0001c0001t0001g0024a0001c0001t0001g0122a0001c0001t0001g0300others(19): Show | 24 | HG00099.hp1 HG00438.hp2 HG00735.hp2 others(21): Show |
intron_variant | MODIFIER | c.1587+85_1587+94del others(10): Show |
GFM2 | ENSG00000164347.18 | transcript | ENST00000296805.8 | protein_coding | 16/20 | chr5 | 74732927 | ||||||
chr5:74732927
|
GACACACA others(5): Show |
G | 15 | a0001c0001t0001g0165a0001c0001t0001g0203a0001c0001t0001g0212others(12): Show | 17 | HG01433.hp1 HG01884.hp2 HG01891.hp1 others(14): Show |
intron_variant | MODIFIER | c.1587+83_1587+94del others(12): Show |
GFM2 | ENSG00000164347.18 | transcript | ENST00000296805.8 | protein_coding | 16/20 | chr5 | 74732927 | ||||||
chr5:74732927
|
GACACACA others(7): Show |
G | 2 | a0001c0001t0001g0118a0002c0002t0001g0146 | 2 | HG02965.hp1 NA18945.hp2 |
intron_variant | MODIFIER | c.1587+81_1587+94del others(14): Show |
GFM2 | ENSG00000164347.18 | transcript | ENST00000296805.8 | protein_coding | 16/20 | chr5 | 74732927 | ||||||
chr5:74732927
|
GACACACA others(13): Show |
G | 10 | a0001c0001t0001g0018a0001c0001t0001g0117a0001c0001t0001g0120others(7): Show | 12 | HG00609.hp1 HG00733.hp2 HG01243.hp1 others(9): Show |
intron_variant | MODIFIER | c.1587+75_1587+94del others(20): Show |
GFM2 | ENSG00000164347.18 | transcript | ENST00000296805.8 | protein_coding | 16/20 | chr5 | 74732927 | ||||||
chr5:74732978
|
A | T | 8 | a0001c0001t0001g0018a0001c0001t0001g0117a0001c0001t0001g0118others(5): Show | 9 | HG00609.hp1 HG02165.hp2 NA18945.hp2 others(6): Show |
intron_variant | MODIFIER | c.1587+44T>A | GFM2 | ENSG00000164347.18 | transcript | ENST00000296805.8 | protein_coding | 16/20 | chr5 | 74732978 | ||||||
chr5:74733229
|
G | T | 1 | a0006c0008t0001g0172 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.1511-131C>A | GFM2 | ENSG00000164347.18 | transcript | ENST00000296805.8 | protein_coding | 15/20 | chr5 | 74733229 | ||||||
chr5:74733335
|
G | GA | 76 | a0001c0011t0002g0042a0001c0011t0002g0070a0002c0002t0001g0019others(73): Show | 88 | HG00099.hp2 HG00408.hp2 HG00438.hp2 others(85): Show |
intron_variant | MODIFIER | c.1511-238dupT | GFM2 | ENSG00000164347.18 | transcript | ENST00000296805.8 | protein_coding | 15/20 | chr5 | 74733335 | ||||||
chr5:74733335
|
GA | G | 12 | a0002c0006t0001g0127a0002c0006t0001g0132a0002c0006t0001g0135others(9): Show | 12 | HG02559.hp1 HG02615.hp2 HG02723.hp2 others(9): Show |
intron_variant | MODIFIER | c.1511-238delT | GFM2 | ENSG00000164347.18 | transcript | ENST00000296805.8 | protein_coding | 15/20 | chr5 | 74733335 | ||||||
chr5:74733388
|
G | A | 1 | a0002c0002t0002g0065 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.1511-290C>T | GFM2 | ENSG00000164347.18 | transcript | ENST00000296805.8 | protein_coding | 15/20 | chr5 | 74733388 | ||||||
chr5:74733511
|
C | T | 1 | a0001c0001t0001g0096 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.1511-413G>A | GFM2 | ENSG00000164347.18 | transcript | ENST00000296805.8 | protein_coding | 15/20 | chr5 | 74733511 | ||||||
chr5:74733517
|
G | A | 1 | a0002c0002t0001g0152 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1511-419C>T | GFM2 | ENSG00000164347.18 | transcript | ENST00000296805.8 | protein_coding | 15/20 | chr5 | 74733517 | ||||||
chr5:74733727
|
T | C | 1 | a0003c0003t0001g0278 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.1511-629A>G | GFM2 | ENSG00000164347.18 | transcript | ENST00000296805.8 | protein_coding | 15/20 | chr5 | 74733727 | ||||||
chr5:74733761
|
A | T | 85 | a0001c0011t0002g0042a0001c0011t0002g0070a0002c0002t0001g0019others(82): Show | 98 | HG00099.hp2 HG00408.hp2 HG00438.hp2 others(95): Show |
intron_variant | MODIFIER | c.1511-663T>A | GFM2 | ENSG00000164347.18 | transcript | ENST00000296805.8 | protein_coding | 15/20 | chr5 | 74733761 | ||||||
chr5:74733973
|
C | CCT | 2 | a0001c0001t0001g0023a0001c0001t0001g0235 | 3 | HG01891.hp2 HG02258.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.1511-877_1511-876d others(4): Show |
GFM2 | ENSG00000164347.18 | transcript | ENST00000296805.8 | protein_coding | 15/20 | chr5 | 74733973 | ||||||
chr5:74734243
|
G | A | 12 | a0002c0006t0001g0127a0002c0006t0001g0132a0002c0006t0001g0135others(9): Show | 12 | HG02559.hp1 HG02615.hp2 HG02723.hp2 others(9): Show |
intron_variant | MODIFIER | c.1511-1145C>T | GFM2 | ENSG00000164347.18 | transcript | ENST00000296805.8 | protein_coding | 15/20 | chr5 | 74734243 | ||||||
chr5:74734256
|
T | C | 73 | a0001c0011t0002g0042a0001c0011t0002g0070a0002c0002t0001g0019others(70): Show | 84 | HG00099.hp2 HG00408.hp2 HG00438.hp2 others(81): Show |
intron_variant | MODIFIER | c.1511-1158A>G | GFM2 | ENSG00000164347.18 | transcript | ENST00000296805.8 | protein_coding | 15/20 | chr5 | 74734256 | ||||||
chr5:74734513
|
G | A | 47 | a0001c0001t0001g0003a0001c0001t0001g0016a0001c0001t0001g0017others(44): Show | 54 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(51): Show |
intron_variant | MODIFIER | c.1511-1415C>T | GFM2 | ENSG00000164347.18 | transcript | ENST00000296805.8 | protein_coding | 15/20 | chr5 | 74734513 | ||||||
chr5:74734540
|
TC | T | 9 | a0002c0005t0001g0034a0002c0005t0001g0040a0002c0005t0001g0244others(6): Show | 11 | HG02145.hp2 HG02451.hp2 HG02559.hp2 others(8): Show |
intron_variant | MODIFIER | c.1511-1443delG | GFM2 | ENSG00000164347.18 | transcript | ENST00000296805.8 | protein_coding | 15/20 | chr5 | 74734540 | ||||||
chr5:74734965
|
C | T | 1 | a0001c0001t0003g0251 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.1510+1831G>A | GFM2 | ENSG00000164347.18 | transcript | ENST00000296805.8 | protein_coding | 15/20 | chr5 | 74734965 | ||||||
chr5:74735194
|
A | T | 2 | a0002c0005t0001g0231a0002c0005t0001g0232 | 2 | HG01891.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.1510+1602T>A | GFM2 | ENSG00000164347.18 | transcript | ENST00000296805.8 | protein_coding | 15/20 | chr5 | 74735194 | ||||||
chr5:74735316
|
T | C | 2 | a0002c0005t0001g0244a0002c0005t0001g0245 | 2 | HG02630.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.1510+1480A>G | GFM2 | ENSG00000164347.18 | transcript | ENST00000296805.8 | protein_coding | 15/20 | chr5 | 74735316 | ||||||
chr5:74735490
|
G | C | 1 | a0002c0002t0002g0065 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.1510+1306C>G | GFM2 | ENSG00000164347.18 | transcript | ENST00000296805.8 | protein_coding | 15/20 | chr5 | 74735490 | ||||||
chr5:74735553
|
G | A | 1 | a0009c0012t0001g0286 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.1510+1243C>T | GFM2 | ENSG00000164347.18 | transcript | ENST00000296805.8 | protein_coding | 15/20 | chr5 | 74735553 | ||||||
chr5:74735700
|
G | A | 36 | a0002c0005t0001g0308a0003c0003t0001g0011a0003c0003t0001g0012others(33): Show | 43 | HG00140.hp1 HG00280.hp2 HG00642.hp2 others(40): Show |
intron_variant | MODIFIER | c.1510+1096C>T | GFM2 | ENSG00000164347.18 | transcript | ENST00000296805.8 | protein_coding | 15/20 | chr5 | 74735700 | ||||||
chr5:74735739
|
A | G | 1 | a0002c0002t0001g0242 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.1510+1057T>C | GFM2 | ENSG00000164347.18 | transcript | ENST00000296805.8 | protein_coding | 15/20 | chr5 | 74735739 | ||||||
chr5:74735871
|
T | C | 2 | a0002c0005t0001g0231a0002c0005t0001g0232 | 2 | HG01891.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.1510+925A>G | GFM2 | ENSG00000164347.18 | transcript | ENST00000296805.8 | protein_coding | 15/20 | chr5 | 74735871 | ||||||
chr5:74736189
|
G | C | 4 | a0001c0001t0001g0254a0001c0001t0003g0035a0001c0001t0003g0247others(1): Show | 5 | HG03654.hp2 NA18965.hp2 NA18987.hp1 others(2): Show |
intron_variant | MODIFIER | c.1510+607C>G | GFM2 | ENSG00000164347.18 | transcript | ENST00000296805.8 | protein_coding | 15/20 | chr5 | 74736189 | ||||||
chr5:74736191
|
A | T | 1 | a0001c0001t0001g0104 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.1510+605T>A | GFM2 | ENSG00000164347.18 | transcript | ENST00000296805.8 | protein_coding | 15/20 | chr5 | 74736191 | ||||||
chr5:74736205
|
G | T | 2 | a0001c0001t0001g0117a0001c0001t0001g0120 | 2 | NA18982.hp2 NA19011.hp1 |
intron_variant | MODIFIER | c.1510+591C>A | GFM2 | ENSG00000164347.18 | transcript | ENST00000296805.8 | protein_coding | 15/20 | chr5 | 74736205 | ||||||
chr5:74736274
|
C | A | 1 | a0002c0002t0002g0066 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.1510+522G>T | GFM2 | ENSG00000164347.18 | transcript | ENST00000296805.8 | protein_coding | 15/20 | chr5 | 74736274 | ||||||
chr5:74736291
|
G | A | 35 | a0003c0003t0001g0011a0003c0003t0001g0012a0003c0003t0001g0038others(32): Show | 42 | HG00140.hp1 HG00280.hp2 HG00642.hp2 others(39): Show |
intron_variant | MODIFIER | c.1510+505C>T | GFM2 | ENSG00000164347.18 | transcript | ENST00000296805.8 | protein_coding | 15/20 | chr5 | 74736291 | ||||||
chr5:74736733
|
T | C | 1 | a0001c0001t0003g0268 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.1510+63A>G | GFM2 | ENSG00000164347.18 | transcript | ENST00000296805.8 | protein_coding | 15/20 | chr5 | 74736733 | ||||||
chr5:74737043
|
C | T | 3 | a0002c0002t0001g0175a0002c0002t0001g0233a0002c0002t0001g0237 | 3 | HG03041.hp1 HG03098.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.1321-58G>A | GFM2 | ENSG00000164347.18 | transcript | ENST00000296805.8 | protein_coding | 14/20 | chr5 | 74737043 | ||||||
chr5:74737072
|
T | C | 35 | a0003c0003t0001g0011a0003c0003t0001g0012a0003c0003t0001g0038others(32): Show | 42 | HG00140.hp1 HG00280.hp2 HG00642.hp2 others(39): Show |
intron_variant | MODIFIER | c.1321-87A>G | GFM2 | ENSG00000164347.18 | transcript | ENST00000296805.8 | protein_coding | 14/20 | chr5 | 74737072 | ||||||
chr5:74737484
|
T | C | 48 | a0001c0011t0002g0042a0001c0011t0002g0070a0002c0002t0002g0002others(45): Show | 57 | HG00099.hp2 HG00408.hp2 HG00558.hp1 others(54): Show |
intron_variant | MODIFIER | c.1321-499A>G | GFM2 | ENSG00000164347.18 | transcript | ENST00000296805.8 | protein_coding | 14/20 | chr5 | 74737484 | ||||||
chr5:74737592
|
T | C | 1 | a0001c0001t0001g0090 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.1321-607A>G | GFM2 | ENSG00000164347.18 | transcript | ENST00000296805.8 | protein_coding | 14/20 | chr5 | 74737592 | ||||||
chr5:74737739
|
G | C | 1 | a0003c0003t0001g0280 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.1320+579C>G | GFM2 | ENSG00000164347.18 | transcript | ENST00000296805.8 | protein_coding | 14/20 | chr5 | 74737739 | ||||||
chr5:74737833
|
A | G | 5 | a0006c0008t0001g0134a0006c0008t0001g0171a0006c0008t0001g0172others(2): Show | 5 | HG00438.hp2 HG00735.hp2 HG02293.hp1 others(2): Show |
intron_variant | MODIFIER | c.1320+485T>C | GFM2 | ENSG00000164347.18 | transcript | ENST00000296805.8 | protein_coding | 14/20 | chr5 | 74737833 | ||||||
chr5:74737872
|
G | A | 1 | a0002c0002t0002g0067 | 1 | NA19065.hp2 | intron_variant | MODIFIER | c.1320+446C>T | GFM2 | ENSG00000164347.18 | transcript | ENST00000296805.8 | protein_coding | 14/20 | chr5 | 74737872 | ||||||
chr5:74737876
|
G | A | 35 | a0003c0003t0001g0011a0003c0003t0001g0012a0003c0003t0001g0038others(32): Show | 42 | HG00140.hp1 HG00280.hp2 HG00642.hp2 others(39): Show |
intron_variant | MODIFIER | c.1320+442C>T | GFM2 | ENSG00000164347.18 | transcript | ENST00000296805.8 | protein_coding | 14/20 | chr5 | 74737876 | ||||||
chr5:74738038
|
A | G | 18 | a0001c0001t0001g0027a0001c0001t0001g0028a0001c0001t0001g0129others(15): Show | 20 | HG00438.hp1 HG00621.hp1 HG02015.hp2 others(17): Show |
intron_variant | MODIFIER | c.1320+280T>C | GFM2 | ENSG00000164347.18 | transcript | ENST00000296805.8 | protein_coding | 14/20 | chr5 | 74738038 | ||||||
chr5:74738119
|
C | T | 134 | a0001c0011t0002g0042a0001c0011t0002g0070a0002c0002t0001g0019others(131): Show | 154 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(151): Show |
intron_variant | MODIFIER | c.1320+199G>A | GFM2 | ENSG00000164347.18 | transcript | ENST00000296805.8 | protein_coding | 14/20 | chr5 | 74738119 | ||||||
chr5:74738207
|
C | A | 9 | a0002c0005t0001g0034a0002c0005t0001g0040a0002c0005t0001g0244others(6): Show | 11 | HG02145.hp2 HG02451.hp2 HG02559.hp2 others(8): Show |
intron_variant | MODIFIER | c.1320+111G>T | GFM2 | ENSG00000164347.18 | transcript | ENST00000296805.8 | protein_coding | 14/20 | chr5 | 74738207 | ||||||
chr5:74738420
|
G | A | 35 | a0003c0003t0001g0011a0003c0003t0001g0012a0003c0003t0001g0038others(32): Show | 42 | HG00140.hp1 HG00280.hp2 HG00642.hp2 others(39): Show |
splice_region_variant&intron_variant | LOW | c.1221-3C>T | GFM2 | ENSG00000164347.18 | transcript | ENST00000296805.8 | protein_coding | 13/20 | chr5 | 74738420 | ||||||
chr5:74738750
|
T | C | 2 | a0005c0009t0001g0153a0005c0009t0001g0154 | 2 | HG02451.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.1080-108A>G | GFM2 | ENSG00000164347.18 | transcript | ENST00000296805.8 | protein_coding | 12/20 | chr5 | 74738750 | ||||||
chr5:74738760
|
AAAT | A | 3 | a0002c0002t0001g0175a0002c0002t0001g0233a0002c0002t0001g0237 | 3 | HG03041.hp1 HG03098.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.1080-121_1080-119d others(5): Show |
GFM2 | ENSG00000164347.18 | transcript | ENST00000296805.8 | protein_coding | 12/20 | chr5 | 74738760 | ||||||
chr5:74738778
|
G | A | 1 | a0001c0001t0003g0268 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.1080-136C>T | GFM2 | ENSG00000164347.18 | transcript | ENST00000296805.8 | protein_coding | 12/20 | chr5 | 74738778 | ||||||
chr5:74738810
|
A | T | 1 | a0002c0002t0001g0243 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.1080-168T>A | GFM2 | ENSG00000164347.18 | transcript | ENST00000296805.8 | protein_coding | 12/20 | chr5 | 74738810 | ||||||
chr5:74738945
|
T | C | 1 | a0001c0001t0001g0087 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.1080-303A>G | GFM2 | ENSG00000164347.18 | transcript | ENST00000296805.8 | protein_coding | 12/20 | chr5 | 74738945 | ||||||
chr5:74738998
|
C | T | 1 | a0003c0003t0001g0290 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.1080-356G>A | GFM2 | ENSG00000164347.18 | transcript | ENST00000296805.8 | protein_coding | 12/20 | chr5 | 74738998 | ||||||
chr5:74738999
|
G | C | 5 | a0006c0008t0001g0134a0006c0008t0001g0171a0006c0008t0001g0172others(2): Show | 5 | HG00438.hp2 HG00735.hp2 HG02293.hp1 others(2): Show |
intron_variant | MODIFIER | c.1080-357C>G | GFM2 | ENSG00000164347.18 | transcript | ENST00000296805.8 | protein_coding | 12/20 | chr5 | 74738999 | ||||||
chr5:74739155
|
T | TGC | 3 | a0002c0002t0001g0175a0002c0002t0001g0233a0002c0002t0001g0237 | 3 | HG03041.hp1 HG03098.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.1080-515_1080-514d others(4): Show |
GFM2 | ENSG00000164347.18 | transcript | ENST00000296805.8 | protein_coding | 12/20 | chr5 | 74739155 | ||||||
chr5:74739158
|
G | A | 1 | a0001c0001t0001g0185 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.1080-516C>T | GFM2 | ENSG00000164347.18 | transcript | ENST00000296805.8 | protein_coding | 12/20 | chr5 | 74739158 | ||||||
chr5:74739160
|
A | C | 25 | a0002c0002t0001g0019a0002c0002t0001g0133a0002c0002t0001g0146others(22): Show | 27 | HG00438.hp2 HG00735.hp2 HG00741.hp2 others(24): Show |
intron_variant | MODIFIER | c.1080-518T>G | GFM2 | ENSG00000164347.18 | transcript | ENST00000296805.8 | protein_coding | 12/20 | chr5 | 74739160 | ||||||
chr5:74739369
|
G | A | 1 | a0001c0001t0001g0180 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.1079+620C>T | GFM2 | ENSG00000164347.18 | transcript | ENST00000296805.8 | protein_coding | 12/20 | chr5 | 74739369 | ||||||
chr5:74739396
|
G | A | 1 | a0002c0002t0002g0068 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.1079+593C>T | GFM2 | ENSG00000164347.18 | transcript | ENST00000296805.8 | protein_coding | 12/20 | chr5 | 74739396 | ||||||
chr5:74739460
|
A | G | 1 | a0001c0001t0001g0217 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.1079+529T>C | GFM2 | ENSG00000164347.18 | transcript | ENST00000296805.8 | protein_coding | 12/20 | chr5 | 74739460 | ||||||
chr5:74739483
|
T | C | 6 | a0005c0007t0001g0037a0005c0007t0001g0270a0005c0007t0001g0271others(3): Show | 7 | HG00733.hp2 HG01243.hp1 HG02109.hp2 others(4): Show |
intron_variant | MODIFIER | c.1079+506A>G | GFM2 | ENSG00000164347.18 | transcript | ENST00000296805.8 | protein_coding | 12/20 | chr5 | 74739483 | ||||||
chr5:74739848
|
C | T | 3 | a0001c0001t0001g0129a0001c0001t0001g0130a0001c0001t0001g0131 | 3 | HG00621.hp1 HG02080.hp2 NA18950.hp2 |
intron_variant | MODIFIER | c.1079+141G>A | GFM2 | ENSG00000164347.18 | transcript | ENST00000296805.8 | protein_coding | 12/20 | chr5 | 74739848 | ||||||
chr5:74739970
|
T | A | 1 | a0002c0002t0002g0069 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.1079+19A>T | GFM2 | ENSG00000164347.18 | transcript | ENST00000296805.8 | protein_coding | 12/20 | chr5 | 74739970 | ||||||
chr5:74740204
|
G | T | 6 | a0002c0002t0001g0238a0002c0002t0001g0239a0002c0002t0001g0240others(3): Show | 6 | HG01884.hp2 HG02280.hp1 HG02647.hp1 others(3): Show |
intron_variant | MODIFIER | c.931-67C>A | GFM2 | ENSG00000164347.18 | transcript | ENST00000296805.8 | protein_coding | 11/20 | chr5 | 74740204 | ||||||
chr5:74740256
|
A | C | 1 | a0001c0001t0003g0265 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.931-119T>G | GFM2 | ENSG00000164347.18 | transcript | ENST00000296805.8 | protein_coding | 11/20 | chr5 | 74740256 | ||||||
chr5:74740330
|
C | T | 2 | a0003c0003t0001g0277a0003c0003t0001g0278 | 2 | HG02572.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.931-193G>A | GFM2 | ENSG00000164347.18 | transcript | ENST00000296805.8 | protein_coding | 11/20 | chr5 | 74740330 | ||||||
chr5:74740338
|
T | C | 1 | a0001c0001t0003g0267 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.931-201A>G | GFM2 | ENSG00000164347.18 | transcript | ENST00000296805.8 | protein_coding | 11/20 | chr5 | 74740338 | ||||||
chr5:74740423
|
A | G | 12 | a0002c0006t0001g0127a0002c0006t0001g0132a0002c0006t0001g0135others(9): Show | 12 | HG02559.hp1 HG02615.hp2 HG02723.hp2 others(9): Show |
intron_variant | MODIFIER | c.931-286T>C | GFM2 | ENSG00000164347.18 | transcript | ENST00000296805.8 | protein_coding | 11/20 | chr5 | 74740423 | ||||||
chr5:74740575
|
A | C | 1 | a0001c0001t0001g0199 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.931-438T>G | GFM2 | ENSG00000164347.18 | transcript | ENST00000296805.8 | protein_coding | 11/20 | chr5 | 74740575 | ||||||
chr5:74740948
|
A | T | 11 | a0002c0002t0001g0019a0002c0002t0001g0133a0002c0002t0001g0146others(8): Show | 13 | HG00741.hp2 HG01106.hp1 HG01167.hp1 others(10): Show |
intron_variant | MODIFIER | c.930+581T>A | GFM2 | ENSG00000164347.18 | transcript | ENST00000296805.8 | protein_coding | 11/20 | chr5 | 74740948 | ||||||
chr5:74740969
|
A | T | 16 | a0001c0001t0001g0004a0001c0001t0001g0008a0001c0001t0001g0024others(13): Show | 24 | HG00323.hp1 HG00733.hp1 HG01884.hp1 others(21): Show |
intron_variant | MODIFIER | c.930+560T>A | GFM2 | ENSG00000164347.18 | transcript | ENST00000296805.8 | protein_coding | 11/20 | chr5 | 74740969 | ||||||
chr5:74741176
|
C | A | 1 | a0001c0001t0003g0251 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.930+353G>T | GFM2 | ENSG00000164347.18 | transcript | ENST00000296805.8 | protein_coding | 11/20 | chr5 | 74741176 | ||||||
chr5:74741178
|
T | C | 1 | a0001c0001t0001g0212 | 1 | NA18957.hp2 | intron_variant | MODIFIER | c.930+351A>G | GFM2 | ENSG00000164347.18 | transcript | ENST00000296805.8 | protein_coding | 11/20 | chr5 | 74741178 | ||||||
chr5:74741680
|
A | G | 9 | a0002c0005t0001g0034a0002c0005t0001g0040a0002c0005t0001g0244others(6): Show | 11 | HG02145.hp2 HG02451.hp2 HG02559.hp2 others(8): Show |
intron_variant | MODIFIER | c.850-71T>C | GFM2 | ENSG00000164347.18 | transcript | ENST00000296805.8 | protein_coding | 10/20 | chr5 | 74741680 | ||||||
chr5:74741814
|
G | A | 3 | a0002c0002t0001g0019a0002c0002t0001g0149a0002c0002t0001g0150 | 4 | HG00741.hp2 HG01106.hp1 HG01167.hp1 others(1): Show |
intron_variant | MODIFIER | c.850-205C>T | GFM2 | ENSG00000164347.18 | transcript | ENST00000296805.8 | protein_coding | 10/20 | chr5 | 74741814 | ||||||
chr5:74742021
|
C | T | 9 | a0002c0005t0001g0034a0002c0005t0001g0040a0002c0005t0001g0244others(6): Show | 11 | HG02145.hp2 HG02451.hp2 HG02559.hp2 others(8): Show |
intron_variant | MODIFIER | c.850-412G>A | GFM2 | ENSG00000164347.18 | transcript | ENST00000296805.8 | protein_coding | 10/20 | chr5 | 74742021 | ||||||
chr5:74742164
|
C | T | 35 | a0003c0003t0001g0011a0003c0003t0001g0012a0003c0003t0001g0038others(32): Show | 42 | HG00140.hp1 HG00280.hp2 HG00642.hp2 others(39): Show |
intron_variant | MODIFIER | c.850-555G>A | GFM2 | ENSG00000164347.18 | transcript | ENST00000296805.8 | protein_coding | 10/20 | chr5 | 74742164 | ||||||
chr5:74742257
|
T | TA | 49 | a0001c0001t0001g0009a0001c0001t0001g0026a0001c0001t0001g0089others(46): Show | 59 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(56): Show |
intron_variant | MODIFIER | c.850-649dupT | GFM2 | ENSG00000164347.18 | transcript | ENST00000296805.8 | protein_coding | 10/20 | chr5 | 74742257 | ||||||
chr5:74742267
|
A | C | 2 | a0002c0005t0001g0231a0002c0005t0001g0232 | 2 | HG01891.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.850-658T>G | GFM2 | ENSG00000164347.18 | transcript | ENST00000296805.8 | protein_coding | 10/20 | chr5 | 74742267 | ||||||
chr5:74742272
|
C | A | 35 | a0003c0003t0001g0011a0003c0003t0001g0012a0003c0003t0001g0038others(32): Show | 42 | HG00140.hp1 HG00280.hp2 HG00642.hp2 others(39): Show |
intron_variant | MODIFIER | c.850-663G>T | GFM2 | ENSG00000164347.18 | transcript | ENST00000296805.8 | protein_coding | 10/20 | chr5 | 74742272 | ||||||
chr5:74742361
|
G | C | 4 | a0006c0008t0001g0134a0006c0008t0001g0172a0006c0008t0001g0174others(1): Show | 4 | HG00438.hp2 HG02293.hp1 NA18982.hp1 others(1): Show |
intron_variant | MODIFIER | c.850-752C>G | GFM2 | ENSG00000164347.18 | transcript | ENST00000296805.8 | protein_coding | 10/20 | chr5 | 74742361 | ||||||
chr5:74742672
|
C | CT | 56 | a0002c0002t0001g0019a0002c0002t0001g0133a0002c0002t0001g0146others(53): Show | 64 | HG00140.hp1 HG00280.hp2 HG00438.hp2 others(61): Show |
intron_variant | MODIFIER | c.850-1064dupA | GFM2 | ENSG00000164347.18 | transcript | ENST00000296805.8 | protein_coding | 10/20 | chr5 | 74742672 | ||||||
chr5:74742980
|
C | A | 29 | a0003c0003t0001g0011a0003c0003t0001g0012a0003c0003t0001g0038others(26): Show | 35 | HG00140.hp1 HG00280.hp2 HG00642.hp2 others(32): Show |
intron_variant | MODIFIER | c.850-1371G>T | GFM2 | ENSG00000164347.18 | transcript | ENST00000296805.8 | protein_coding | 10/20 | chr5 | 74742980 | ||||||
chr5:74743050
|
A | G | 1 | a0002c0005t0001g0310 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.850-1441T>C | GFM2 | ENSG00000164347.18 | transcript | ENST00000296805.8 | protein_coding | 10/20 | chr5 | 74743050 | ||||||
chr5:74743141
|
A | T | 9 | a0002c0005t0001g0034a0002c0005t0001g0040a0002c0005t0001g0244others(6): Show | 11 | HG02145.hp2 HG02451.hp2 HG02559.hp2 others(8): Show |
intron_variant | MODIFIER | c.850-1532T>A | GFM2 | ENSG00000164347.18 | transcript | ENST00000296805.8 | protein_coding | 10/20 | chr5 | 74743141 | ||||||
chr5:74743325
|
C | A | 76 | a0001c0011t0002g0042a0001c0011t0002g0070a0002c0002t0001g0019others(73): Show | 87 | HG00099.hp2 HG00408.hp2 HG00438.hp2 others(84): Show |
intron_variant | MODIFIER | c.850-1716G>T | GFM2 | ENSG00000164347.18 | transcript | ENST00000296805.8 | protein_coding | 10/20 | chr5 | 74743325 | ||||||
chr5:74743347
|
G | A | 1 | a0001c0001t0001g0187 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.850-1738C>T | GFM2 | ENSG00000164347.18 | transcript | ENST00000296805.8 | protein_coding | 10/20 | chr5 | 74743347 | ||||||
chr5:74743354
|
C | A | 1 | a0002c0002t0001g0151 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.850-1745G>T | GFM2 | ENSG00000164347.18 | transcript | ENST00000296805.8 | protein_coding | 10/20 | chr5 | 74743354 | ||||||
chr5:74743438
|
C | T | 35 | a0003c0003t0001g0011a0003c0003t0001g0012a0003c0003t0001g0038others(32): Show | 42 | HG00140.hp1 HG00280.hp2 HG00642.hp2 others(39): Show |
intron_variant | MODIFIER | c.850-1829G>A | GFM2 | ENSG00000164347.18 | transcript | ENST00000296805.8 | protein_coding | 10/20 | chr5 | 74743438 | ||||||
chr5:74743559
|
T | A | 1 | a0002c0006t0001g0142 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.850-1950A>T | GFM2 | ENSG00000164347.18 | transcript | ENST00000296805.8 | protein_coding | 10/20 | chr5 | 74743559 | ||||||
chr5:74743588
|
G | A | 1 | a0001c0001t0001g0211 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.850-1979C>T | GFM2 | ENSG00000164347.18 | transcript | ENST00000296805.8 | protein_coding | 10/20 | chr5 | 74743588 | ||||||
chr5:74743636
|
T | C | 2 | a0001c0001t0001g0023a0001c0001t0001g0235 | 3 | HG01891.hp2 HG02258.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.850-2027A>G | GFM2 | ENSG00000164347.18 | transcript | ENST00000296805.8 | protein_coding | 10/20 | chr5 | 74743636 | ||||||
chr5:74743856
|
G | A | 2 | a0001c0001t0001g0165a0001c0001t0001g0212 | 2 | HG01981.hp2 NA18957.hp2 |
intron_variant | MODIFIER | c.849+1822C>T | GFM2 | ENSG00000164347.18 | transcript | ENST00000296805.8 | protein_coding | 10/20 | chr5 | 74743856 | ||||||
chr5:74744017
|
T | C | 2 | a0001c0001t0001g0195a0001c0001t0001g0215 | 2 | HG02015.hp2 NA18954.hp2 |
intron_variant | MODIFIER | c.849+1661A>G | GFM2 | ENSG00000164347.18 | transcript | ENST00000296805.8 | protein_coding | 10/20 | chr5 | 74744017 | ||||||
chr5:74744043
|
G | C | 1 | a0001c0001t0001g0181 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.849+1635C>G | GFM2 | ENSG00000164347.18 | transcript | ENST00000296805.8 | protein_coding | 10/20 | chr5 | 74744043 | ||||||
chr5:74744184
|
CCATACAG others(4): Show |
C | 35 | a0003c0003t0001g0011a0003c0003t0001g0012a0003c0003t0001g0038others(32): Show | 42 | HG00140.hp1 HG00280.hp2 HG00642.hp2 others(39): Show |
intron_variant | MODIFIER | c.849+1483_849+1493d others(13): Show |
GFM2 | ENSG00000164347.18 | transcript | ENST00000296805.8 | protein_coding | 10/20 | chr5 | 74744184 | ||||||
chr5:74744196
|
T | A | 35 | a0003c0003t0001g0011a0003c0003t0001g0012a0003c0003t0001g0038others(32): Show | 42 | HG00140.hp1 HG00280.hp2 HG00642.hp2 others(39): Show |
intron_variant | MODIFIER | c.849+1482A>T | GFM2 | ENSG00000164347.18 | transcript | ENST00000296805.8 | protein_coding | 10/20 | chr5 | 74744196 | ||||||
chr5:74744362
|
TA | T | 35 | a0003c0003t0001g0011a0003c0003t0001g0012a0003c0003t0001g0038others(32): Show | 42 | HG00140.hp1 HG00280.hp2 HG00642.hp2 others(39): Show |
intron_variant | MODIFIER | c.849+1315delT | GFM2 | ENSG00000164347.18 | transcript | ENST00000296805.8 | protein_coding | 10/20 | chr5 | 74744362 | ||||||
chr5:74744393
|
G | GA | 48 | a0001c0011t0002g0042a0001c0011t0002g0070a0002c0002t0002g0002others(45): Show | 57 | HG00099.hp2 HG00408.hp2 HG00558.hp1 others(54): Show |
intron_variant | MODIFIER | c.849+1284dupT | GFM2 | ENSG00000164347.18 | transcript | ENST00000296805.8 | protein_coding | 10/20 | chr5 | 74744393 | ||||||
chr5:74744615
|
T | C | 2 | a0002c0002t0001g0233a0002c0002t0001g0237 | 2 | HG03041.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.849+1063A>G | GFM2 | ENSG00000164347.18 | transcript | ENST00000296805.8 | protein_coding | 10/20 | chr5 | 74744615 | ||||||
chr5:74744686
|
A | C | 1 | a0002c0002t0001g0133 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.849+992T>G | GFM2 | ENSG00000164347.18 | transcript | ENST00000296805.8 | protein_coding | 10/20 | chr5 | 74744686 | ||||||
chr5:74744782
|
T | C | 3 | a0001c0001t0001g0213a0002c0005t0001g0231a0002c0005t0001g0232 | 3 | HG01891.hp1 HG02129.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.849+896A>G | GFM2 | ENSG00000164347.18 | transcript | ENST00000296805.8 | protein_coding | 10/20 | chr5 | 74744782 | ||||||
chr5:74744791
|
T | A | 1 | a0001c0001t0001g0186 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.849+887A>T | GFM2 | ENSG00000164347.18 | transcript | ENST00000296805.8 | protein_coding | 10/20 | chr5 | 74744791 | ||||||
chr5:74744927
|
A | G | 2 | a0002c0005t0001g0231a0002c0005t0001g0232 | 2 | HG01891.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.849+751T>C | GFM2 | ENSG00000164347.18 | transcript | ENST00000296805.8 | protein_coding | 10/20 | chr5 | 74744927 | ||||||
chr5:74745054
|
T | C | 1 | a0005c0007t0001g0274 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.849+624A>G | GFM2 | ENSG00000164347.18 | transcript | ENST00000296805.8 | protein_coding | 10/20 | chr5 | 74745054 | ||||||
chr5:74745057
|
G | A | 28 | a0001c0001t0001g0254a0001c0001t0003g0006a0001c0001t0003g0035others(25): Show | 35 | HG00673.hp1 HG00741.hp1 HG01123.hp2 others(32): Show |
intron_variant | MODIFIER | c.849+621C>T | GFM2 | ENSG00000164347.18 | transcript | ENST00000296805.8 | protein_coding | 10/20 | chr5 | 74745057 | ||||||
chr5:74745136
|
G | A | 1 | a0001c0001t0001g0187 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.849+542C>T | GFM2 | ENSG00000164347.18 | transcript | ENST00000296805.8 | protein_coding | 10/20 | chr5 | 74745136 | ||||||
chr5:74745280
|
G | C | 1 | a0001c0001t0001g0084 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.849+398C>G | GFM2 | ENSG00000164347.18 | transcript | ENST00000296805.8 | protein_coding | 10/20 | chr5 | 74745280 | ||||||
chr5:74745299
|
T | C | 248 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0008others(245): Show | 292 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(289): Show |
intron_variant | MODIFIER | c.849+379A>G | GFM2 | ENSG00000164347.18 | transcript | ENST00000296805.8 | protein_coding | 10/20 | chr5 | 74745299 | ||||||
chr5:74745440
|
G | T | 1 | a0001c0001t0001g0103 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.849+238C>A | GFM2 | ENSG00000164347.18 | transcript | ENST00000296805.8 | protein_coding | 10/20 | chr5 | 74745440 | ||||||
chr5:74745481
|
A | G | 6 | a0005c0007t0001g0037a0005c0007t0001g0270a0005c0007t0001g0271others(3): Show | 7 | HG00733.hp2 HG01243.hp1 HG02109.hp2 others(4): Show |
intron_variant | MODIFIER | c.849+197T>C | GFM2 | ENSG00000164347.18 | transcript | ENST00000296805.8 | protein_coding | 10/20 | chr5 | 74745481 | ||||||
chr5:74745504
|
C | G | 36 | a0001c0001t0001g0100a0003c0003t0001g0011a0003c0003t0001g0012others(33): Show | 43 | HG00140.hp1 HG00280.hp2 HG00642.hp2 others(40): Show |
intron_variant | MODIFIER | c.849+174G>C | GFM2 | ENSG00000164347.18 | transcript | ENST00000296805.8 | protein_coding | 10/20 | chr5 | 74745504 | ||||||
chr5:74745961
|
A | AT | 36 | a0001c0001t0001g0100a0003c0003t0001g0011a0003c0003t0001g0012others(33): Show | 43 | HG00140.hp1 HG00280.hp2 HG00642.hp2 others(40): Show |
intron_variant | MODIFIER | c.670-105dupA | GFM2 | ENSG00000164347.18 | transcript | ENST00000296805.8 | protein_coding | 9/20 | chr5 | 74745961 | ||||||
chr5:74746175
|
G | A | 1 | a0007c0010t0001g0188 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.609-10C>T | GFM2 | ENSG00000164347.18 | transcript | ENST00000296805.8 | protein_coding | 8/20 | chr5 | 74746175 | ||||||
chr5:74746301
|
C | A | 1 | a0002c0002t0002g0078 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.609-136G>T | GFM2 | ENSG00000164347.18 | transcript | ENST00000296805.8 | protein_coding | 8/20 | chr5 | 74746301 | ||||||
chr5:74746399
|
T | TA | 3 | a0002c0002t0002g0041a0002c0002t0002g0071a0002c0002t0002g0073 | 3 | NA18949.hp1 NA18974.hp2 NA19011.hp2 |
intron_variant | MODIFIER | c.609-235dupT | GFM2 | ENSG00000164347.18 | transcript | ENST00000296805.8 | protein_coding | 8/20 | chr5 | 74746399 | ||||||
chr5:74746403
|
G | T | 3 | a0001c0001t0001g0021a0001c0001t0001g0156a0001c0001t0001g0157 | 4 | HG02809.hp2 HG03041.hp2 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.609-238C>A | GFM2 | ENSG00000164347.18 | transcript | ENST00000296805.8 | protein_coding | 8/20 | chr5 | 74746403 | ||||||
chr5:74746418
|
G | A | 1 | a0001c0001t0001g0224 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.609-253C>T | GFM2 | ENSG00000164347.18 | transcript | ENST00000296805.8 | protein_coding | 8/20 | chr5 | 74746418 | ||||||
chr5:74746451
|
A | G | 1 | a0005c0007t0001g0272 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.609-286T>C | GFM2 | ENSG00000164347.18 | transcript | ENST00000296805.8 | protein_coding | 8/20 | chr5 | 74746451 | ||||||
chr5:74746500
|
A | G | 3 | a0001c0001t0001g0027a0001c0001t0001g0155a0001c0001t0001g0159 | 4 | NA18955.hp1 NA19003.hp2 NA19065.hp1 others(1): Show |
intron_variant | MODIFIER | c.609-335T>C | GFM2 | ENSG00000164347.18 | transcript | ENST00000296805.8 | protein_coding | 8/20 | chr5 | 74746500 | ||||||
chr5:74746507
|
A | T | 1 | a0002c0002t0002g0054 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.609-342T>A | GFM2 | ENSG00000164347.18 | transcript | ENST00000296805.8 | protein_coding | 8/20 | chr5 | 74746507 | ||||||
chr5:74746624
|
T | C | 2 | a0002c0005t0001g0231a0002c0005t0001g0232 | 2 | HG01891.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.609-459A>G | GFM2 | ENSG00000164347.18 | transcript | ENST00000296805.8 | protein_coding | 8/20 | chr5 | 74746624 | ||||||
chr5:74746961
|
T | C | 12 | a0002c0006t0001g0127a0002c0006t0001g0132a0002c0006t0001g0135others(9): Show | 12 | HG02559.hp1 HG02615.hp2 HG02723.hp2 others(9): Show |
intron_variant | MODIFIER | c.608+731A>G | GFM2 | ENSG00000164347.18 | transcript | ENST00000296805.8 | protein_coding | 8/20 | chr5 | 74746961 | ||||||
chr5:74746987
|
T | C | 1 | a0001c0001t0003g0268 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.608+705A>G | GFM2 | ENSG00000164347.18 | transcript | ENST00000296805.8 | protein_coding | 8/20 | chr5 | 74746987 | ||||||
chr5:74747067
|
C | G | 1 | a0005c0007t0001g0271 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.608+625G>C | GFM2 | ENSG00000164347.18 | transcript | ENST00000296805.8 | protein_coding | 8/20 | chr5 | 74747067 | ||||||
chr5:74747138
|
C | T | 1 | a0014c0016t0002g0053 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.608+554G>A | GFM2 | ENSG00000164347.18 | transcript | ENST00000296805.8 | protein_coding | 8/20 | chr5 | 74747138 | ||||||
chr5:74747220
|
G | C | 12 | a0002c0006t0001g0127a0002c0006t0001g0132a0002c0006t0001g0135others(9): Show | 12 | HG02559.hp1 HG02615.hp2 HG02723.hp2 others(9): Show |
intron_variant | MODIFIER | c.608+472C>G | GFM2 | ENSG00000164347.18 | transcript | ENST00000296805.8 | protein_coding | 8/20 | chr5 | 74747220 | ||||||
chr5:74747252
|
G | A | 2 | a0001c0001t0001g0090a0001c0001t0001g0115 | 2 | HG03195.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.608+440C>T | GFM2 | ENSG00000164347.18 | transcript | ENST00000296805.8 | protein_coding | 8/20 | chr5 | 74747252 | ||||||
chr5:74747356
|
G | A | 9 | a0002c0005t0001g0034a0002c0005t0001g0040a0002c0005t0001g0244others(6): Show | 11 | HG02145.hp2 HG02451.hp2 HG02559.hp2 others(8): Show |
intron_variant | MODIFIER | c.608+336C>T | GFM2 | ENSG00000164347.18 | transcript | ENST00000296805.8 | protein_coding | 8/20 | chr5 | 74747356 | ||||||
chr5:74747361
|
A | G | 1 | a0002c0002t0002g0041 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.608+331T>C | GFM2 | ENSG00000164347.18 | transcript | ENST00000296805.8 | protein_coding | 8/20 | chr5 | 74747361 | ||||||
chr5:74747575
|
T | G | 1 | a0001c0001t0001g0213 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.608+117A>C | GFM2 | ENSG00000164347.18 | transcript | ENST00000296805.8 | protein_coding | 8/20 | chr5 | 74747575 | ||||||
chr5:74747813
|
G | C | 2 | a0002c0002t0002g0072a0002c0002t0002g0076 | 2 | HG01109.hp1 HG01346.hp2 |
intron_variant | MODIFIER | c.520-33C>G | GFM2 | ENSG00000164347.18 | transcript | ENST00000296805.8 | protein_coding | 7/20 | chr5 | 74747813 | ||||||
chr5:74747958
|
C | T | 6 | a0005c0007t0001g0037a0005c0007t0001g0270a0005c0007t0001g0271others(3): Show | 7 | HG00733.hp2 HG01243.hp1 HG02109.hp2 others(4): Show |
intron_variant | MODIFIER | c.520-178G>A | GFM2 | ENSG00000164347.18 | transcript | ENST00000296805.8 | protein_coding | 7/20 | chr5 | 74747958 | ||||||
chr5:74748109
|
C | T | 243 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0008others(240): Show | 285 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(282): Show |
intron_variant | MODIFIER | c.520-329G>A | GFM2 | ENSG00000164347.18 | transcript | ENST00000296805.8 | protein_coding | 7/20 | chr5 | 74748109 | ||||||
chr5:74748332
|
T | C | 1 | a0001c0001t0001g0195 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.520-552A>G | GFM2 | ENSG00000164347.18 | transcript | ENST00000296805.8 | protein_coding | 7/20 | chr5 | 74748332 | ||||||
chr5:74748607
|
G | A | 1 | a0001c0001t0001g0304 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.520-827C>T | GFM2 | ENSG00000164347.18 | transcript | ENST00000296805.8 | protein_coding | 7/20 | chr5 | 74748607 | ||||||
chr5:74748780
|
G | A | 30 | a0001c0001t0001g0100a0003c0003t0001g0011a0003c0003t0001g0012others(27): Show | 36 | HG00140.hp1 HG00280.hp2 HG00642.hp2 others(33): Show |
intron_variant | MODIFIER | c.520-1000C>T | GFM2 | ENSG00000164347.18 | transcript | ENST00000296805.8 | protein_coding | 7/20 | chr5 | 74748780 | ||||||
chr5:74748784
|
G | A | 76 | a0001c0011t0002g0042a0001c0011t0002g0070a0002c0002t0001g0019others(73): Show | 87 | HG00099.hp2 HG00408.hp2 HG00438.hp2 others(84): Show |
intron_variant | MODIFIER | c.520-1004C>T | GFM2 | ENSG00000164347.18 | transcript | ENST00000296805.8 | protein_coding | 7/20 | chr5 | 74748784 | ||||||
chr5:74748843
|
C | A | 9 | a0003c0003t0001g0012a0003c0003t0001g0275a0003c0003t0001g0276others(6): Show | 11 | HG00140.hp1 HG00280.hp2 HG00738.hp2 others(8): Show |
intron_variant | MODIFIER | c.520-1063G>T | GFM2 | ENSG00000164347.18 | transcript | ENST00000296805.8 | protein_coding | 7/20 | chr5 | 74748843 | ||||||
chr5:74748890
|
T | TAAATA | 67 | a0001c0011t0002g0042a0001c0011t0002g0070a0002c0002t0001g0151others(64): Show | 76 | HG00099.hp2 HG00408.hp2 HG00438.hp2 others(73): Show |
intron_variant | MODIFIER | c.520-1115_520-1111d others(7): Show |
GFM2 | ENSG00000164347.18 | transcript | ENST00000296805.8 | protein_coding | 7/20 | chr5 | 74748890 | ||||||
chr5:74748890
|
T | TAAATAAA others(3): Show |
9 | a0002c0002t0001g0233a0002c0005t0001g0034a0002c0005t0001g0040others(6): Show | 11 | HG02145.hp2 HG02451.hp2 HG02559.hp2 others(8): Show |
intron_variant | MODIFIER | c.520-1120_520-1111d others(12): Show |
GFM2 | ENSG00000164347.18 | transcript | ENST00000296805.8 | protein_coding | 7/20 | chr5 | 74748890 | ||||||
chr5:74748890
|
T | TAAATAAA others(8): Show |
1 | a0002c0005t0001g0245 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.520-1125_520-1111d others(17): Show |
GFM2 | ENSG00000164347.18 | transcript | ENST00000296805.8 | protein_coding | 7/20 | chr5 | 74748890 | ||||||
chr5:74748909
|
TAAA | T | 14 | a0002c0006t0001g0127a0002c0006t0001g0132a0002c0006t0001g0136others(11): Show | 14 | HG00642.hp2 HG01361.hp1 HG02559.hp1 others(11): Show |
intron_variant | MODIFIER | c.520-1132_520-1130d others(5): Show |
GFM2 | ENSG00000164347.18 | transcript | ENST00000296805.8 | protein_coding | 7/20 | chr5 | 74748909 | ||||||
chr5:74748909
|
TAAAAA | T | 24 | a0001c0001t0001g0003a0001c0001t0001g0017a0001c0001t0001g0018others(21): Show | 30 | HG00609.hp1 HG01074.hp2 HG01099.hp1 others(27): Show |
intron_variant | MODIFIER | c.520-1134_520-1130d others(7): Show |
GFM2 | ENSG00000164347.18 | transcript | ENST00000296805.8 | protein_coding | 7/20 | chr5 | 74748909 | ||||||
chr5:74748912
|
A | AAT | 26 | a0001c0001t0001g0100a0003c0003t0001g0011a0003c0003t0001g0012others(23): Show | 32 | HG00140.hp1 HG00280.hp2 HG00738.hp2 others(29): Show |
intron_variant | MODIFIER | c.520-1133_520-1132i others(4): Show |
GFM2 | ENSG00000164347.18 | transcript | ENST00000296805.8 | protein_coding | 7/20 | chr5 | 74748912 | ||||||
chr5:74748914
|
A | T | 92 | a0001c0011t0002g0042a0001c0011t0002g0070a0002c0002t0001g0019others(89): Show | 106 | HG00099.hp2 HG00408.hp2 HG00438.hp2 others(103): Show |
intron_variant | MODIFIER | c.520-1134T>A | GFM2 | ENSG00000164347.18 | transcript | ENST00000296805.8 | protein_coding | 7/20 | chr5 | 74748914 | ||||||
chr5:74748917
|
T | A | 7 | a0003c0003t0001g0287a0005c0007t0001g0037a0005c0007t0001g0270others(4): Show | 8 | HG00733.hp2 HG01243.hp1 HG02109.hp2 others(5): Show |
intron_variant | MODIFIER | c.520-1137A>T | GFM2 | ENSG00000164347.18 | transcript | ENST00000296805.8 | protein_coding | 7/20 | chr5 | 74748917 | ||||||
chr5:74748917
|
TA | T | 6 | a0001c0001t0001g0225a0001c0001t0001g0226a0001c0001t0001g0228others(3): Show | 6 | HG02145.hp1 HG02615.hp1 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.520-1138delT | GFM2 | ENSG00000164347.18 | transcript | ENST00000296805.8 | protein_coding | 7/20 | chr5 | 74748917 | ||||||
chr5:74748919
|
A | AAAT | 17 | a0003c0003t0001g0011a0003c0003t0001g0012a0003c0003t0001g0038others(14): Show | 22 | HG00140.hp1 HG00280.hp2 HG00738.hp2 others(19): Show |
intron_variant | MODIFIER | c.520-1140_520-1139i others(5): Show |
GFM2 | ENSG00000164347.18 | transcript | ENST00000296805.8 | protein_coding | 7/20 | chr5 | 74748919 | ||||||
chr5:74748919
|
A | T | 7 | a0003c0003t0001g0287a0005c0007t0001g0037a0005c0007t0001g0270others(4): Show | 8 | HG00733.hp2 HG01243.hp1 HG02109.hp2 others(5): Show |
intron_variant | MODIFIER | c.520-1139T>A | GFM2 | ENSG00000164347.18 | transcript | ENST00000296805.8 | protein_coding | 7/20 | chr5 | 74748919 | ||||||
chr5:74748922
|
A | T | 11 | a0001c0001t0001g0100a0003c0003t0001g0039a0003c0003t0001g0276others(8): Show | 12 | HG01243.hp2 HG01361.hp1 HG02165.hp1 others(9): Show |
intron_variant | MODIFIER | c.520-1142T>A | GFM2 | ENSG00000164347.18 | transcript | ENST00000296805.8 | protein_coding | 7/20 | chr5 | 74748922 | ||||||
chr5:74748925
|
A | T | 12 | a0002c0006t0001g0127a0002c0006t0001g0132a0002c0006t0001g0136others(9): Show | 12 | HG00642.hp2 HG02559.hp1 HG02615.hp2 others(9): Show |
intron_variant | MODIFIER | c.520-1145T>A | GFM2 | ENSG00000164347.18 | transcript | ENST00000296805.8 | protein_coding | 7/20 | chr5 | 74748925 | ||||||
chr5:74748926
|
AT | A | 12 | a0002c0006t0001g0127a0002c0006t0001g0132a0002c0006t0001g0136others(9): Show | 12 | HG00642.hp2 HG02559.hp1 HG02615.hp2 others(9): Show |
intron_variant | MODIFIER | c.520-1147delA | GFM2 | ENSG00000164347.18 | transcript | ENST00000296805.8 | protein_coding | 7/20 | chr5 | 74748926 | ||||||
chr5:74748927
|
T | TA | 24 | a0003c0003t0001g0011a0003c0003t0001g0012a0003c0003t0001g0038others(21): Show | 30 | HG00140.hp1 HG00280.hp2 HG00733.hp2 others(27): Show |
intron_variant | MODIFIER | c.520-1148dupT | GFM2 | ENSG00000164347.18 | transcript | ENST00000296805.8 | protein_coding | 7/20 | chr5 | 74748927 | ||||||
chr5:74748927
|
T | TAAAAAAA others(2): Show |
9 | a0001c0001t0001g0100a0003c0003t0001g0039a0003c0003t0001g0281others(6): Show | 10 | HG01243.hp2 HG02165.hp1 HG02735.hp1 others(7): Show |
intron_variant | MODIFIER | c.520-1148_520-1147i others(11): Show |
GFM2 | ENSG00000164347.18 | transcript | ENST00000296805.8 | protein_coding | 7/20 | chr5 | 74748927 | ||||||
chr5:74748938
|
AAAAATAA others(8): Show |
A | 1 | a0001c0001t0001g0196 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.520-1173_520-1159d others(17): Show |
GFM2 | ENSG00000164347.18 | transcript | ENST00000296805.8 | protein_coding | 7/20 | chr5 | 74748938 | ||||||
chr5:74748942
|
AT | A | 11 | a0002c0006t0001g0127a0002c0006t0001g0132a0002c0006t0001g0136others(8): Show | 11 | HG02559.hp1 HG02615.hp2 HG02723.hp2 others(8): Show |
intron_variant | MODIFIER | c.520-1163delA | GFM2 | ENSG00000164347.18 | transcript | ENST00000296805.8 | protein_coding | 7/20 | chr5 | 74748942 | ||||||
chr5:74748943
|
T | A | 2 | a0003c0003t0001g0276a0009c0012t0001g0286 | 2 | HG01361.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.520-1163A>T | GFM2 | ENSG00000164347.18 | transcript | ENST00000296805.8 | protein_coding | 7/20 | chr5 | 74748943 | ||||||
chr5:74748943
|
T | C | 9 | a0002c0005t0001g0034a0002c0005t0001g0040a0002c0005t0001g0244others(6): Show | 11 | HG02145.hp2 HG02451.hp2 HG02559.hp2 others(8): Show |
intron_variant | MODIFIER | c.520-1163A>G | GFM2 | ENSG00000164347.18 | transcript | ENST00000296805.8 | protein_coding | 7/20 | chr5 | 74748943 | ||||||
chr5:74748946
|
A | T | 13 | a0002c0006t0001g0127a0002c0006t0001g0132a0002c0006t0001g0136others(10): Show | 13 | HG01361.hp1 HG02559.hp1 HG02615.hp2 others(10): Show |
intron_variant | MODIFIER | c.520-1166T>A | GFM2 | ENSG00000164347.18 | transcript | ENST00000296805.8 | protein_coding | 7/20 | chr5 | 74748946 | ||||||
chr5:74748948
|
T | A | 13 | a0002c0006t0001g0127a0002c0006t0001g0132a0002c0006t0001g0136others(10): Show | 13 | HG01361.hp1 HG02559.hp1 HG02615.hp2 others(10): Show |
intron_variant | MODIFIER | c.520-1168A>T | GFM2 | ENSG00000164347.18 | transcript | ENST00000296805.8 | protein_coding | 7/20 | chr5 | 74748948 | ||||||
chr5:74748963
|
TAAAGA | T | 5 | a0002c0002t0001g0238a0002c0002t0001g0239a0002c0002t0001g0240others(2): Show | 5 | HG01884.hp2 HG02647.hp1 HG02809.hp1 others(2): Show |
intron_variant | MODIFIER | c.520-1188_520-1184d others(7): Show |
GFM2 | ENSG00000164347.18 | transcript | ENST00000296805.8 | protein_coding | 7/20 | chr5 | 74748963 | ||||||
chr5:74749528
|
T | C | 1 | a0001c0001t0001g0214 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.519+1051A>G | GFM2 | ENSG00000164347.18 | transcript | ENST00000296805.8 | protein_coding | 7/20 | chr5 | 74749528 | ||||||
chr5:74749731
|
C | T | 12 | a0002c0006t0001g0127a0002c0006t0001g0132a0002c0006t0001g0135others(9): Show | 12 | HG02559.hp1 HG02615.hp2 HG02723.hp2 others(9): Show |
intron_variant | MODIFIER | c.519+848G>A | GFM2 | ENSG00000164347.18 | transcript | ENST00000296805.8 | protein_coding | 7/20 | chr5 | 74749731 | ||||||
chr5:74749756
|
T | C | 12 | a0002c0006t0001g0127a0002c0006t0001g0132a0002c0006t0001g0135others(9): Show | 12 | HG02559.hp1 HG02615.hp2 HG02723.hp2 others(9): Show |
intron_variant | MODIFIER | c.519+823A>G | GFM2 | ENSG00000164347.18 | transcript | ENST00000296805.8 | protein_coding | 7/20 | chr5 | 74749756 | ||||||
chr5:74749815
|
T | A | 1 | a0001c0001t0001g0166 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.519+764A>T | GFM2 | ENSG00000164347.18 | transcript | ENST00000296805.8 | protein_coding | 7/20 | chr5 | 74749815 | ||||||
chr5:74750398
|
C | A | 1 | a0001c0001t0001g0026 | 2 | HG00323.hp1 HG03669.hp1 |
intron_variant | MODIFIER | c.519+181G>T | GFM2 | ENSG00000164347.18 | transcript | ENST00000296805.8 | protein_coding | 7/20 | chr5 | 74750398 | ||||||
chr5:74750694
|
C | T | 1 | a0002c0002t0002g0050 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.431-27G>A | GFM2 | ENSG00000164347.18 | transcript | ENST00000296805.8 | protein_coding | 6/20 | chr5 | 74750694 | ||||||
chr5:74750831
|
A | G | 35 | a0003c0003t0001g0011a0003c0003t0001g0012a0003c0003t0001g0038others(32): Show | 42 | HG00140.hp1 HG00280.hp2 HG00642.hp2 others(39): Show |
intron_variant | MODIFIER | c.431-164T>C | GFM2 | ENSG00000164347.18 | transcript | ENST00000296805.8 | protein_coding | 6/20 | chr5 | 74750831 | ||||||
chr5:74751057
|
C | T | 1 | a0001c0001t0001g0100 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.430+311G>A | GFM2 | ENSG00000164347.18 | transcript | ENST00000296805.8 | protein_coding | 6/20 | chr5 | 74751057 | ||||||
chr5:74751611
|
G | A | 29 | a0003c0003t0001g0011a0003c0003t0001g0012a0003c0003t0001g0038others(26): Show | 35 | HG00140.hp1 HG00280.hp2 HG00642.hp2 others(32): Show |
intron_variant | MODIFIER | c.305-118C>T | GFM2 | ENSG00000164347.18 | transcript | ENST00000296805.8 | protein_coding | 5/20 | chr5 | 74751611 | ||||||
chr5:74751867
|
C | T | 76 | a0001c0011t0002g0042a0001c0011t0002g0070a0002c0002t0001g0019others(73): Show | 87 | HG00099.hp2 HG00408.hp2 HG00438.hp2 others(84): Show |
intron_variant | MODIFIER | c.305-374G>A | GFM2 | ENSG00000164347.18 | transcript | ENST00000296805.8 | protein_coding | 5/20 | chr5 | 74751867 | ||||||
chr5:74751956
|
C | A | 1 | a0002c0002t0002g0073 | 1 | NA18949.hp1 | intron_variant | MODIFIER | c.305-463G>T | GFM2 | ENSG00000164347.18 | transcript | ENST00000296805.8 | protein_coding | 5/20 | chr5 | 74751956 | ||||||
chr5:74752138
|
T | G | 35 | a0003c0003t0001g0011a0003c0003t0001g0012a0003c0003t0001g0038others(32): Show | 42 | HG00140.hp1 HG00280.hp2 HG00642.hp2 others(39): Show |
intron_variant | MODIFIER | c.305-645A>C | GFM2 | ENSG00000164347.18 | transcript | ENST00000296805.8 | protein_coding | 5/20 | chr5 | 74752138 | ||||||
chr5:74752296
|
T | G | 12 | a0004c0004t0001g0264a0004c0004t0003g0010a0004c0004t0003g0248others(9): Show | 14 | NA18943.hp2 NA18944.hp2 NA18962.hp1 others(11): Show |
intron_variant | MODIFIER | c.305-803A>C | GFM2 | ENSG00000164347.18 | transcript | ENST00000296805.8 | protein_coding | 5/20 | chr5 | 74752296 | ||||||
chr5:74752311
|
T | G | 1 | a0001c0001t0001g0301 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.305-818A>C | GFM2 | ENSG00000164347.18 | transcript | ENST00000296805.8 | protein_coding | 5/20 | chr5 | 74752311 | ||||||
chr5:74752325
|
C | A | 35 | a0003c0003t0001g0011a0003c0003t0001g0012a0003c0003t0001g0038others(32): Show | 42 | HG00140.hp1 HG00280.hp2 HG00642.hp2 others(39): Show |
intron_variant | MODIFIER | c.305-832G>T | GFM2 | ENSG00000164347.18 | transcript | ENST00000296805.8 | protein_coding | 5/20 | chr5 | 74752325 | ||||||
chr5:74752374
|
T | C | 3 | a0002c0002t0002g0046a0002c0002t0002g0074a0002c0002t0002g0075 | 3 | HG02135.hp2 NA18952.hp2 NA19005.hp2 |
intron_variant | MODIFIER | c.305-881A>G | GFM2 | ENSG00000164347.18 | transcript | ENST00000296805.8 | protein_coding | 5/20 | chr5 | 74752374 | ||||||
chr5:74752424
|
C | T | 12 | a0002c0006t0001g0127a0002c0006t0001g0132a0002c0006t0001g0135others(9): Show | 12 | HG02559.hp1 HG02615.hp2 HG02723.hp2 others(9): Show |
intron_variant | MODIFIER | c.305-931G>A | GFM2 | ENSG00000164347.18 | transcript | ENST00000296805.8 | protein_coding | 5/20 | chr5 | 74752424 | ||||||
chr5:74752662
|
C | A | 5 | a0001c0001t0001g0017a0001c0001t0001g0091a0001c0001t0001g0097others(2): Show | 6 | HG01099.hp1 HG01168.hp2 HG01169.hp2 others(3): Show |
intron_variant | MODIFIER | c.305-1169G>T | GFM2 | ENSG00000164347.18 | transcript | ENST00000296805.8 | protein_coding | 5/20 | chr5 | 74752662 | ||||||
chr5:74753221
|
C | G | 29 | a0003c0003t0001g0011a0003c0003t0001g0012a0003c0003t0001g0038others(26): Show | 35 | HG00140.hp1 HG00280.hp2 HG00642.hp2 others(32): Show |
intron_variant | MODIFIER | c.305-1728G>C | GFM2 | ENSG00000164347.18 | transcript | ENST00000296805.8 | protein_coding | 5/20 | chr5 | 74753221 | ||||||
chr5:74753273
|
G | T | 1 | a0002c0002t0001g0302 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.305-1780C>A | GFM2 | ENSG00000164347.18 | transcript | ENST00000296805.8 | protein_coding | 5/20 | chr5 | 74753273 | ||||||
chr5:74753283
|
T | C | 1 | a0011c0017t0001g0145 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.305-1790A>G | GFM2 | ENSG00000164347.18 | transcript | ENST00000296805.8 | protein_coding | 5/20 | chr5 | 74753283 | ||||||
chr5:74753371
|
G | A | 16 | a0001c0001t0001g0004a0001c0001t0001g0008a0001c0001t0001g0024others(13): Show | 24 | HG00323.hp1 HG00733.hp1 HG01884.hp1 others(21): Show |
intron_variant | MODIFIER | c.305-1878C>T | GFM2 | ENSG00000164347.18 | transcript | ENST00000296805.8 | protein_coding | 5/20 | chr5 | 74753371 | ||||||
chr5:74753511
|
T | C | 35 | a0003c0003t0001g0011a0003c0003t0001g0012a0003c0003t0001g0038others(32): Show | 42 | HG00140.hp1 HG00280.hp2 HG00642.hp2 others(39): Show |
intron_variant | MODIFIER | c.305-2018A>G | GFM2 | ENSG00000164347.18 | transcript | ENST00000296805.8 | protein_coding | 5/20 | chr5 | 74753511 | ||||||
chr5:74753957
|
T | TG | 76 | a0001c0011t0002g0042a0001c0011t0002g0070a0002c0002t0001g0019others(73): Show | 87 | HG00099.hp2 HG00408.hp2 HG00438.hp2 others(84): Show |
intron_variant | MODIFIER | c.305-2465dupC | GFM2 | ENSG00000164347.18 | transcript | ENST00000296805.8 | protein_coding | 5/20 | chr5 | 74753957 | ||||||
chr5:74754115
|
G | T | 1 | a0002c0006t0001g0135 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.305-2622C>A | GFM2 | ENSG00000164347.18 | transcript | ENST00000296805.8 | protein_coding | 5/20 | chr5 | 74754115 | ||||||
chr5:74754206
|
A | T | 1 | a0001c0001t0001g0221 | 1 | NA18957.hp1 | intron_variant | MODIFIER | c.305-2713T>A | GFM2 | ENSG00000164347.18 | transcript | ENST00000296805.8 | protein_coding | 5/20 | chr5 | 74754206 | ||||||
chr5:74754208
|
A | G | 1 | a0007c0010t0001g0234 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.305-2715T>C | GFM2 | ENSG00000164347.18 | transcript | ENST00000296805.8 | protein_coding | 5/20 | chr5 | 74754208 | ||||||
chr5:74754305
|
GA | G | 75 | a0001c0001t0001g0182a0002c0002t0001g0019a0002c0002t0001g0133others(72): Show | 86 | HG00280.hp2 HG00438.hp2 HG00642.hp2 others(83): Show |
intron_variant | MODIFIER | c.305-2813delT | GFM2 | ENSG00000164347.18 | transcript | ENST00000296805.8 | protein_coding | 5/20 | chr5 | 74754305 | ||||||
chr5:74754305
|
GAA | G | 47 | a0001c0011t0002g0042a0001c0011t0002g0070a0002c0002t0002g0002others(44): Show | 56 | HG00099.hp2 HG00408.hp2 HG00558.hp1 others(53): Show |
intron_variant | MODIFIER | c.305-2814_305-2813d others(4): Show |
GFM2 | ENSG00000164347.18 | transcript | ENST00000296805.8 | protein_coding | 5/20 | chr5 | 74754305 | ||||||
chr5:74754319
|
A | C | 35 | a0003c0003t0001g0011a0003c0003t0001g0012a0003c0003t0001g0038others(32): Show | 42 | HG00140.hp1 HG00280.hp2 HG00642.hp2 others(39): Show |
intron_variant | MODIFIER | c.305-2826T>G | GFM2 | ENSG00000164347.18 | transcript | ENST00000296805.8 | protein_coding | 5/20 | chr5 | 74754319 | ||||||
chr5:74754359
|
C | A | 1 | a0001c0001t0001g0215 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.305-2866G>T | GFM2 | ENSG00000164347.18 | transcript | ENST00000296805.8 | protein_coding | 5/20 | chr5 | 74754359 | ||||||
chr5:74754370
|
A | G | 1 | a0002c0002t0002g0052 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.305-2877T>C | GFM2 | ENSG00000164347.18 | transcript | ENST00000296805.8 | protein_coding | 5/20 | chr5 | 74754370 | ||||||
chr5:74754384
|
G | T | 132 | a0001c0011t0002g0042a0001c0011t0002g0070a0002c0002t0001g0019others(129): Show | 152 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(149): Show |
intron_variant | MODIFIER | c.305-2891C>A | GFM2 | ENSG00000164347.18 | transcript | ENST00000296805.8 | protein_coding | 5/20 | chr5 | 74754384 | ||||||
chr5:74754446
|
G | A | 35 | a0003c0003t0001g0011a0003c0003t0001g0012a0003c0003t0001g0038others(32): Show | 42 | HG00140.hp1 HG00280.hp2 HG00642.hp2 others(39): Show |
intron_variant | MODIFIER | c.305-2953C>T | GFM2 | ENSG00000164347.18 | transcript | ENST00000296805.8 | protein_coding | 5/20 | chr5 | 74754446 | ||||||
chr5:74754490
|
A | C | 133 | a0001c0011t0002g0042a0001c0011t0002g0070a0002c0002t0001g0019others(130): Show | 153 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(150): Show |
intron_variant | MODIFIER | c.305-2997T>G | GFM2 | ENSG00000164347.18 | transcript | ENST00000296805.8 | protein_coding | 5/20 | chr5 | 74754490 | ||||||
chr5:74754490
|
A | G | 1 | a0002c0005t0001g0309 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.305-2997T>C | GFM2 | ENSG00000164347.18 | transcript | ENST00000296805.8 | protein_coding | 5/20 | chr5 | 74754490 | ||||||
chr5:74754602
|
T | TA | 27 | a0003c0003t0001g0011a0003c0003t0001g0012a0003c0003t0001g0038others(24): Show | 33 | HG00140.hp1 HG00280.hp2 HG00738.hp2 others(30): Show |
intron_variant | MODIFIER | c.305-3110dupT | GFM2 | ENSG00000164347.18 | transcript | ENST00000296805.8 | protein_coding | 5/20 | chr5 | 74754602 | ||||||
chr5:74754615
|
G | A | 12 | a0002c0006t0001g0127a0002c0006t0001g0132a0002c0006t0001g0135others(9): Show | 12 | HG02559.hp1 HG02615.hp2 HG02723.hp2 others(9): Show |
intron_variant | MODIFIER | c.305-3122C>T | GFM2 | ENSG00000164347.18 | transcript | ENST00000296805.8 | protein_coding | 5/20 | chr5 | 74754615 | ||||||
chr5:74754662
|
C | T | 2 | a0001c0001t0001g0098a0001c0001t0001g0304 | 2 | HG00609.hp2 HG00621.hp2 |
intron_variant | MODIFIER | c.305-3169G>A | GFM2 | ENSG00000164347.18 | transcript | ENST00000296805.8 | protein_coding | 5/20 | chr5 | 74754662 | ||||||
chr5:74754927
|
C | T | 85 | a0001c0011t0002g0042a0001c0011t0002g0070a0002c0002t0001g0019others(82): Show | 98 | HG00099.hp2 HG00408.hp2 HG00438.hp2 others(95): Show |
intron_variant | MODIFIER | c.305-3434G>A | GFM2 | ENSG00000164347.18 | transcript | ENST00000296805.8 | protein_coding | 5/20 | chr5 | 74754927 | ||||||
chr5:74754955
|
G | A | 4 | a0002c0002t0002g0015a0002c0002t0002g0047a0002c0002t0002g0077others(1): Show | 5 | NA18953.hp2 NA18975.hp2 NA18988.hp1 others(2): Show |
intron_variant | MODIFIER | c.305-3462C>T | GFM2 | ENSG00000164347.18 | transcript | ENST00000296805.8 | protein_coding | 5/20 | chr5 | 74754955 | ||||||
chr5:74755018
|
C | G | 1 | a0001c0001t0001g0084 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.305-3525G>C | GFM2 | ENSG00000164347.18 | transcript | ENST00000296805.8 | protein_coding | 5/20 | chr5 | 74755018 | ||||||
chr5:74755020
|
C | T | 2 | a0002c0005t0001g0231a0002c0005t0001g0232 | 2 | HG01891.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.305-3527G>A | GFM2 | ENSG00000164347.18 | transcript | ENST00000296805.8 | protein_coding | 5/20 | chr5 | 74755020 | ||||||
chr5:74755075
|
G | A | 1 | a0002c0002t0002g0048 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.305-3582C>T | GFM2 | ENSG00000164347.18 | transcript | ENST00000296805.8 | protein_coding | 5/20 | chr5 | 74755075 | ||||||
chr5:74755302
|
T | C | 9 | a0002c0005t0001g0034a0002c0005t0001g0040a0002c0005t0001g0244others(6): Show | 11 | HG02145.hp2 HG02451.hp2 HG02559.hp2 others(8): Show |
intron_variant | MODIFIER | c.304+3547A>G | GFM2 | ENSG00000164347.18 | transcript | ENST00000296805.8 | protein_coding | 5/20 | chr5 | 74755302 | ||||||
chr5:74755407
|
T | A | 134 | a0001c0011t0002g0042a0001c0011t0002g0070a0002c0002t0001g0019others(131): Show | 154 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(151): Show |
intron_variant | MODIFIER | c.304+3442A>T | GFM2 | ENSG00000164347.18 | transcript | ENST00000296805.8 | protein_coding | 5/20 | chr5 | 74755407 | ||||||
chr5:74755860
|
A | C | 4 | a0001c0001t0001g0087a0001c0001t0001g0098a0001c0001t0001g0304others(1): Show | 4 | HG00609.hp2 HG00621.hp2 HG02083.hp2 others(1): Show |
intron_variant | MODIFIER | c.304+2989T>G | GFM2 | ENSG00000164347.18 | transcript | ENST00000296805.8 | protein_coding | 5/20 | chr5 | 74755860 | ||||||
chr5:74755862
|
G | A | 1 | a0001c0001t0001g0216 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.304+2987C>T | GFM2 | ENSG00000164347.18 | transcript | ENST00000296805.8 | protein_coding | 5/20 | chr5 | 74755862 | ||||||
chr5:74755932
|
C | T | 2 | a0002c0005t0001g0231a0002c0005t0001g0232 | 2 | HG01891.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.304+2917G>A | GFM2 | ENSG00000164347.18 | transcript | ENST00000296805.8 | protein_coding | 5/20 | chr5 | 74755932 | ||||||
chr5:74756031
|
C | T | 5 | a0006c0008t0001g0134a0006c0008t0001g0171a0006c0008t0001g0172others(2): Show | 5 | HG00438.hp2 HG00735.hp2 HG02293.hp1 others(2): Show |
intron_variant | MODIFIER | c.304+2818G>A | GFM2 | ENSG00000164347.18 | transcript | ENST00000296805.8 | protein_coding | 5/20 | chr5 | 74756031 | ||||||
chr5:74756065
|
C | G | 1 | a0005c0009t0001g0154 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.304+2784G>C | GFM2 | ENSG00000164347.18 | transcript | ENST00000296805.8 | protein_coding | 5/20 | chr5 | 74756065 | ||||||
chr5:74756296
|
CCA | C | 16 | a0001c0001t0001g0004a0001c0001t0001g0008a0001c0001t0001g0024others(13): Show | 24 | HG00323.hp1 HG00733.hp1 HG01884.hp1 others(21): Show |
intron_variant | MODIFIER | c.304+2551_304+2552d others(4): Show |
GFM2 | ENSG00000164347.18 | transcript | ENST00000296805.8 | protein_coding | 5/20 | chr5 | 74756296 | ||||||
chr5:74756595
|
G | A | 4 | a0006c0008t0001g0134a0006c0008t0001g0172a0006c0008t0001g0174others(1): Show | 4 | HG00438.hp2 HG02293.hp1 NA18982.hp1 others(1): Show |
intron_variant | MODIFIER | c.304+2254C>T | GFM2 | ENSG00000164347.18 | transcript | ENST00000296805.8 | protein_coding | 5/20 | chr5 | 74756595 | ||||||
chr5:74756665
|
G | GTA | 74 | a0001c0001t0001g0113a0001c0001t0001g0220a0002c0002t0001g0019others(71): Show | 85 | HG00140.hp1 HG00280.hp2 HG00438.hp2 others(82): Show |
intron_variant | MODIFIER | c.304+2182_304+2183d others(4): Show |
GFM2 | ENSG00000164347.18 | transcript | ENST00000296805.8 | protein_coding | 5/20 | chr5 | 74756665 | ||||||
chr5:74756670
|
T | TAC | 48 | a0001c0011t0002g0042a0001c0011t0002g0070a0002c0002t0002g0002others(45): Show | 57 | HG00099.hp2 HG00408.hp2 HG00558.hp1 others(54): Show |
intron_variant | MODIFIER | c.304+2178_304+2179i others(4): Show |
GFM2 | ENSG00000164347.18 | transcript | ENST00000296805.8 | protein_coding | 5/20 | chr5 | 74756670 | ||||||
chr5:74756681
|
A | G | 1 | a0001c0001t0001g0221 | 1 | NA18957.hp1 | intron_variant | MODIFIER | c.304+2168T>C | GFM2 | ENSG00000164347.18 | transcript | ENST00000296805.8 | protein_coding | 5/20 | chr5 | 74756681 | ||||||
chr5:74756808
|
AG | A | 6 | a0002c0002t0001g0238a0002c0002t0001g0239a0002c0002t0001g0240others(3): Show | 6 | HG01884.hp2 HG02280.hp1 HG02647.hp1 others(3): Show |
intron_variant | MODIFIER | c.304+2040delC | GFM2 | ENSG00000164347.18 | transcript | ENST00000296805.8 | protein_coding | 5/20 | chr5 | 74756808 | ||||||
chr5:74756844
|
T | C | 9 | a0002c0005t0001g0034a0002c0005t0001g0040a0002c0005t0001g0244others(6): Show | 11 | HG02145.hp2 HG02451.hp2 HG02559.hp2 others(8): Show |
intron_variant | MODIFIER | c.304+2005A>G | GFM2 | ENSG00000164347.18 | transcript | ENST00000296805.8 | protein_coding | 5/20 | chr5 | 74756844 | ||||||
chr5:74756949
|
G | A | 1 | a0001c0001t0001g0217 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.304+1900C>T | GFM2 | ENSG00000164347.18 | transcript | ENST00000296805.8 | protein_coding | 5/20 | chr5 | 74756949 | ||||||
chr5:74757340
|
CT | C | 9 | a0002c0005t0001g0034a0002c0005t0001g0040a0002c0005t0001g0244others(6): Show | 11 | HG02145.hp2 HG02451.hp2 HG02559.hp2 others(8): Show |
intron_variant | MODIFIER | c.304+1508delA | GFM2 | ENSG00000164347.18 | transcript | ENST00000296805.8 | protein_coding | 5/20 | chr5 | 74757340 | ||||||
chr5:74757702
|
C | T | 1 | a0001c0001t0001g0197 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.304+1147G>A | GFM2 | ENSG00000164347.18 | transcript | ENST00000296805.8 | protein_coding | 5/20 | chr5 | 74757702 | ||||||
chr5:74757730
|
CTAAAA | C | 5 | a0002c0002t0001g0238a0002c0002t0001g0240a0002c0002t0001g0241others(2): Show | 5 | HG01884.hp2 HG02280.hp1 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.304+1114_304+1118d others(7): Show |
GFM2 | ENSG00000164347.18 | transcript | ENST00000296805.8 | protein_coding | 5/20 | chr5 | 74757730 | ||||||
chr5:74757731
|
T | TA | 7 | a0001c0001t0001g0129a0001c0001t0001g0167a0001c0001t0001g0168others(4): Show | 7 | HG00621.hp1 HG01361.hp2 HG02074.hp2 others(4): Show |
intron_variant | MODIFIER | c.304+1117dupT | GFM2 | ENSG00000164347.18 | transcript | ENST00000296805.8 | protein_coding | 5/20 | chr5 | 74757731 | ||||||
chr5:74757731
|
TA | T | 101 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0008others(98): Show | 125 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(122): Show |
intron_variant | MODIFIER | c.304+1117delT | GFM2 | ENSG00000164347.18 | transcript | ENST00000296805.8 | protein_coding | 5/20 | chr5 | 74757731 | ||||||
chr5:74757731
|
TAA | T | 6 | a0001c0001t0001g0096a0001c0001t0001g0097a0001c0001t0001g0225others(3): Show | 6 | HG00642.hp2 HG01168.hp2 HG01516.hp2 others(3): Show |
intron_variant | MODIFIER | c.304+1116_304+1117d others(4): Show |
GFM2 | ENSG00000164347.18 | transcript | ENST00000296805.8 | protein_coding | 5/20 | chr5 | 74757731 | ||||||
chr5:74757731
|
TAAAA | T | 37 | a0002c0002t0004g0079a0002c0005t0001g0231a0002c0005t0001g0232others(34): Show | 44 | HG00140.hp1 HG00280.hp2 HG00733.hp2 others(41): Show |
intron_variant | MODIFIER | c.304+1114_304+1117d others(6): Show |
GFM2 | ENSG00000164347.18 | transcript | ENST00000296805.8 | protein_coding | 5/20 | chr5 | 74757731 | ||||||
chr5:74757731
|
TAAAAA | T | 88 | a0001c0011t0002g0042a0001c0011t0002g0070a0002c0002t0001g0019others(85): Show | 101 | HG00099.hp2 HG00408.hp2 HG00438.hp2 others(98): Show |
intron_variant | MODIFIER | c.304+1113_304+1117d others(7): Show |
GFM2 | ENSG00000164347.18 | transcript | ENST00000296805.8 | protein_coding | 5/20 | chr5 | 74757731 | ||||||
chr5:74757758
|
T | A | 1 | a0001c0001t0001g0116 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.304+1091A>T | GFM2 | ENSG00000164347.18 | transcript | ENST00000296805.8 | protein_coding | 5/20 | chr5 | 74757758 | ||||||
chr5:74757774
|
G | A | 24 | a0002c0002t0001g0019a0002c0002t0001g0133a0002c0002t0001g0146others(21): Show | 26 | HG00438.hp2 HG00735.hp2 HG00741.hp2 others(23): Show |
intron_variant | MODIFIER | c.304+1075C>T | GFM2 | ENSG00000164347.18 | transcript | ENST00000296805.8 | protein_coding | 5/20 | chr5 | 74757774 | ||||||
chr5:74757860
|
C | T | 1 | a0001c0001t0003g0255 | 1 | HG02273.hp2 | intron_variant | MODIFIER | c.304+989G>A | GFM2 | ENSG00000164347.18 | transcript | ENST00000296805.8 | protein_coding | 5/20 | chr5 | 74757860 | ||||||
chr5:74757919
|
T | C | 5 | a0002c0002t0001g0133a0002c0002t0001g0152a0005c0009t0001g0020others(2): Show | 6 | HG02451.hp1 HG02486.hp2 HG02717.hp1 others(3): Show |
intron_variant | MODIFIER | c.304+930A>G | GFM2 | ENSG00000164347.18 | transcript | ENST00000296805.8 | protein_coding | 5/20 | chr5 | 74757919 | ||||||
chr5:74757939
|
A | G | 134 | a0001c0011t0002g0042a0001c0011t0002g0070a0002c0002t0001g0019others(131): Show | 154 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(151): Show |
intron_variant | MODIFIER | c.304+910T>C | GFM2 | ENSG00000164347.18 | transcript | ENST00000296805.8 | protein_coding | 5/20 | chr5 | 74757939 | ||||||
chr5:74758269
|
T | C | 2 | a0002c0005t0001g0231a0002c0005t0001g0232 | 2 | HG01891.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.304+580A>G | GFM2 | ENSG00000164347.18 | transcript | ENST00000296805.8 | protein_coding | 5/20 | chr5 | 74758269 | ||||||
chr5:74758420
|
T | C | 3 | a0001c0001t0003g0252a0001c0001t0003g0255a0001c0001t0003g0256 | 3 | HG02273.hp2 NA18953.hp1 NA19055.hp2 |
intron_variant | MODIFIER | c.304+429A>G | GFM2 | ENSG00000164347.18 | transcript | ENST00000296805.8 | protein_coding | 5/20 | chr5 | 74758420 | ||||||
chr5:74758436
|
T | G | 1 | a0001c0001t0001g0301 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.304+413A>C | GFM2 | ENSG00000164347.18 | transcript | ENST00000296805.8 | protein_coding | 5/20 | chr5 | 74758436 | ||||||
chr5:74758569
|
C | T | 1 | a0002c0002t0001g0175 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.304+280G>A | GFM2 | ENSG00000164347.18 | transcript | ENST00000296805.8 | protein_coding | 5/20 | chr5 | 74758569 | ||||||
chr5:74758625
|
C | T | 1 | a0004c0004t0003g0257 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.304+224G>A | GFM2 | ENSG00000164347.18 | transcript | ENST00000296805.8 | protein_coding | 5/20 | chr5 | 74758625 | ||||||
chr5:74758629
|
T | G | 1 | a0001c0001t0001g0235 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.304+220A>C | GFM2 | ENSG00000164347.18 | transcript | ENST00000296805.8 | protein_coding | 5/20 | chr5 | 74758629 | ||||||
chr5:74758770
|
A | G | 134 | a0001c0011t0002g0042a0001c0011t0002g0070a0002c0002t0001g0019others(131): Show | 154 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(151): Show |
intron_variant | MODIFIER | c.304+79T>C | GFM2 | ENSG00000164347.18 | transcript | ENST00000296805.8 | protein_coding | 5/20 | chr5 | 74758770 | ||||||
chr5:74758816
|
G | A | 1 | a0001c0001t0001g0169 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.304+33C>T | GFM2 | ENSG00000164347.18 | transcript | ENST00000296805.8 | protein_coding | 5/20 | chr5 | 74758816 | ||||||
chr5:74758967
|
AG | A | 35 | a0003c0003t0001g0011a0003c0003t0001g0012a0003c0003t0001g0038others(32): Show | 42 | HG00140.hp1 HG00280.hp2 HG00642.hp2 others(39): Show |
intron_variant | MODIFIER | c.207-22delC | GFM2 | ENSG00000164347.18 | transcript | ENST00000296805.8 | protein_coding | 4/20 | chr5 | 74758967 | ||||||
chr5:74759225
|
G | A | 1 | a0002c0002t0001g0152 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.206+144C>T | GFM2 | ENSG00000164347.18 | transcript | ENST00000296805.8 | protein_coding | 4/20 | chr5 | 74759225 | ||||||
chr5:74759251
|
T | TAAAATTG others(55): Show |
1 | a0002c0006t0001g0136 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.206+117_206+118ins others(62): Show |
GFM2 | ENSG00000164347.18 | transcript | ENST00000296805.8 | protein_coding | 4/20 | chr5 | 74759251 | ||||||
chr5:74759251
|
T | TAAAATTG others(56): Show |
4 | a0002c0006t0001g0132a0002c0006t0001g0137a0002c0006t0001g0138others(1): Show | 4 | HG02723.hp2 HG03139.hp1 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.206+117_206+118ins others(63): Show |
GFM2 | ENSG00000164347.18 | transcript | ENST00000296805.8 | protein_coding | 4/20 | chr5 | 74759251 | ||||||
chr5:74759251
|
T | TAAAATTG others(57): Show |
5 | a0002c0006t0001g0127a0002c0006t0001g0135a0002c0006t0001g0140others(2): Show | 5 | HG02559.hp1 HG03130.hp1 HG03453.hp1 others(2): Show |
intron_variant | MODIFIER | c.206+117_206+118ins others(64): Show |
GFM2 | ENSG00000164347.18 | transcript | ENST00000296805.8 | protein_coding | 4/20 | chr5 | 74759251 | ||||||
chr5:74759251
|
T | TAAAATTG others(58): Show |
2 | a0002c0006t0001g0143a0012c0019t0001g0144 | 2 | HG02615.hp2 HG02886.hp2 |
intron_variant | MODIFIER | c.206+117_206+118ins others(65): Show |
GFM2 | ENSG00000164347.18 | transcript | ENST00000296805.8 | protein_coding | 4/20 | chr5 | 74759251 | ||||||
chr5:74759256
|
T | C | 1 | a0003c0003t0001g0297 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.206+113A>G | GFM2 | ENSG00000164347.18 | transcript | ENST00000296805.8 | protein_coding | 4/20 | chr5 | 74759256 | ||||||
chr5:74759297
|
T | A | 1 | a0001c0001t0001g0221 | 1 | NA18957.hp1 | intron_variant | MODIFIER | c.206+72A>T | GFM2 | ENSG00000164347.18 | transcript | ENST00000296805.8 | protein_coding | 4/20 | chr5 | 74759297 | ||||||
chr5:74759456
|
T | C | 1 | a0002c0002t0002g0050 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.149-30A>G | GFM2 | ENSG00000164347.18 | transcript | ENST00000296805.8 | protein_coding | 3/20 | chr5 | 74759456 | ||||||
chr5:74759593
|
A | T | 1 | a0001c0001t0001g0095 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.149-167T>A | GFM2 | ENSG00000164347.18 | transcript | ENST00000296805.8 | protein_coding | 3/20 | chr5 | 74759593 | ||||||
chr5:74759862
|
T | C | 1 | a0001c0001t0001g0122 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.149-436A>G | GFM2 | ENSG00000164347.18 | transcript | ENST00000296805.8 | protein_coding | 3/20 | chr5 | 74759862 | ||||||
chr5:74759914
|
T | G | 2 | a0002c0005t0001g0231a0002c0005t0001g0232 | 2 | HG01891.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.149-488A>C | GFM2 | ENSG00000164347.18 | transcript | ENST00000296805.8 | protein_coding | 3/20 | chr5 | 74759914 | ||||||
chr5:74760074
|
AAGGCAGT others(9): Show |
A | 1 | a0001c0001t0001g0122 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.149-664_149-649del others(16): Show |
GFM2 | ENSG00000164347.18 | transcript | ENST00000296805.8 | protein_coding | 3/20 | chr5 | 74760074 | ||||||
chr5:74760105
|
C | G | 2 | a0002c0005t0001g0231a0002c0005t0001g0232 | 2 | HG01891.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.149-679G>C | GFM2 | ENSG00000164347.18 | transcript | ENST00000296805.8 | protein_coding | 3/20 | chr5 | 74760105 | ||||||
chr5:74760197
|
T | C | 1 | a0007c0010t0001g0222 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.148+705A>G | GFM2 | ENSG00000164347.18 | transcript | ENST00000296805.8 | protein_coding | 3/20 | chr5 | 74760197 | ||||||
chr5:74760639
|
T | C | 2 | a0001c0001t0001g0229a0001c0001t0001g0230 | 2 | HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.148+263A>G | GFM2 | ENSG00000164347.18 | transcript | ENST00000296805.8 | protein_coding | 3/20 | chr5 | 74760639 | ||||||
chr5:74760659
|
C | T | 8 | a0001c0001t0001g0254a0001c0001t0003g0035a0001c0001t0003g0246others(5): Show | 9 | HG00673.hp1 HG02273.hp2 HG03654.hp2 others(6): Show |
intron_variant | MODIFIER | c.148+243G>A | GFM2 | ENSG00000164347.18 | transcript | ENST00000296805.8 | protein_coding | 3/20 | chr5 | 74760659 | ||||||
chr5:74760688
|
T | C | 40 | a0003c0003t0001g0011a0003c0003t0001g0012a0003c0003t0001g0038others(37): Show | 47 | HG00140.hp1 HG00280.hp2 HG00438.hp2 others(44): Show |
intron_variant | MODIFIER | c.148+214A>G | GFM2 | ENSG00000164347.18 | transcript | ENST00000296805.8 | protein_coding | 3/20 | chr5 | 74760688 | ||||||
chr5:74760850
|
A | G | 2 | a0001c0001t0001g0023a0001c0001t0001g0235 | 3 | HG01891.hp2 HG02258.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.148+52T>C | GFM2 | ENSG00000164347.18 | transcript | ENST00000296805.8 | protein_coding | 3/20 | chr5 | 74760850 | ||||||
chr5:74761262
|
T | C | 1 | a0002c0002t0001g0302 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.64-276A>G | GFM2 | ENSG00000164347.18 | transcript | ENST00000296805.8 | protein_coding | 2/20 | chr5 | 74761262 | ||||||
chr5:74761889
|
G | A | 35 | a0003c0003t0001g0011a0003c0003t0001g0012a0003c0003t0001g0038others(32): Show | 42 | HG00140.hp1 HG00280.hp2 HG00642.hp2 others(39): Show |
intron_variant | MODIFIER | c.64-903C>T | GFM2 | ENSG00000164347.18 | transcript | ENST00000296805.8 | protein_coding | 2/20 | chr5 | 74761889 | ||||||
chr5:74761973
|
T | C | 3 | a0002c0002t0001g0175a0002c0002t0001g0233a0002c0002t0001g0237 | 3 | HG03041.hp1 HG03098.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.64-987A>G | GFM2 | ENSG00000164347.18 | transcript | ENST00000296805.8 | protein_coding | 2/20 | chr5 | 74761973 | ||||||
chr5:74762012
|
G | A | 2 | a0001c0001t0001g0223a0008c0013t0001g0298 | 2 | HG01243.hp2 HG03834.hp1 |
intron_variant | MODIFIER | c.64-1026C>T | GFM2 | ENSG00000164347.18 | transcript | ENST00000296805.8 | protein_coding | 2/20 | chr5 | 74762012 | ||||||
chr5:74762029
|
G | A | 1 | a0001c0001t0001g0170 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.64-1043C>T | GFM2 | ENSG00000164347.18 | transcript | ENST00000296805.8 | protein_coding | 2/20 | chr5 | 74762029 | ||||||
chr5:74762258
|
C | T | 134 | a0001c0011t0002g0042a0001c0011t0002g0070a0002c0002t0001g0019others(131): Show | 154 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(151): Show |
intron_variant | MODIFIER | c.64-1272G>A | GFM2 | ENSG00000164347.18 | transcript | ENST00000296805.8 | protein_coding | 2/20 | chr5 | 74762258 | ||||||
chr5:74762393
|
T | C | 4 | a0002c0002t0002g0051a0002c0002t0002g0080a0002c0002t0002g0081others(1): Show | 4 | HG00099.hp2 HG01069.hp2 HG01071.hp2 others(1): Show |
intron_variant | MODIFIER | c.63+1287A>G | GFM2 | ENSG00000164347.18 | transcript | ENST00000296805.8 | protein_coding | 2/20 | chr5 | 74762393 | ||||||
chr5:74762435
|
T | C | 134 | a0001c0011t0002g0042a0001c0011t0002g0070a0002c0002t0001g0019others(131): Show | 154 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(151): Show |
intron_variant | MODIFIER | c.63+1245A>G | GFM2 | ENSG00000164347.18 | transcript | ENST00000296805.8 | protein_coding | 2/20 | chr5 | 74762435 | ||||||
chr5:74762524
|
T | TACCATAG others(3): Show |
1 | a0001c0001t0001g0122 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.63+1155_63+1156ins others(10): Show |
GFM2 | ENSG00000164347.18 | transcript | ENST00000296805.8 | protein_coding | 2/20 | chr5 | 74762524 | ||||||
chr5:74762573
|
G | T | 217 | a0001c0001t0001g0003a0001c0001t0001g0016a0001c0001t0001g0017others(214): Show | 251 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(248): Show |
intron_variant | MODIFIER | c.63+1107C>A | GFM2 | ENSG00000164347.18 | transcript | ENST00000296805.8 | protein_coding | 2/20 | chr5 | 74762573 | ||||||
chr5:74762628
|
T | A | 1 | a0001c0001t0001g0122 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.63+1052A>T | GFM2 | ENSG00000164347.18 | transcript | ENST00000296805.8 | protein_coding | 2/20 | chr5 | 74762628 | ||||||
chr5:74762638
|
C | CAACTTGC others(5): Show |
1 | a0001c0001t0001g0122 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.63+1041_63+1042ins others(12): Show |
GFM2 | ENSG00000164347.18 | transcript | ENST00000296805.8 | protein_coding | 2/20 | chr5 | 74762638 | ||||||
chr5:74762641
|
T | G | 1 | a0001c0001t0001g0122 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.63+1039A>C | GFM2 | ENSG00000164347.18 | transcript | ENST00000296805.8 | protein_coding | 2/20 | chr5 | 74762641 | ||||||
chr5:74762644
|
T | C | 1 | a0001c0001t0001g0122 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.63+1036A>G | GFM2 | ENSG00000164347.18 | transcript | ENST00000296805.8 | protein_coding | 2/20 | chr5 | 74762644 | ||||||
chr5:74762646
|
T | G | 1 | a0001c0001t0001g0122 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.63+1034A>C | GFM2 | ENSG00000164347.18 | transcript | ENST00000296805.8 | protein_coding | 2/20 | chr5 | 74762646 | ||||||
chr5:74762649
|
C | T | 1 | a0005c0007t0001g0270 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.63+1031G>A | GFM2 | ENSG00000164347.18 | transcript | ENST00000296805.8 | protein_coding | 2/20 | chr5 | 74762649 | ||||||
chr5:74762650
|
G | A | 8 | a0001c0001t0001g0018a0001c0001t0001g0117a0001c0001t0001g0118others(5): Show | 9 | HG00609.hp1 HG02165.hp2 NA18945.hp2 others(6): Show |
intron_variant | MODIFIER | c.63+1030C>T | GFM2 | ENSG00000164347.18 | transcript | ENST00000296805.8 | protein_coding | 2/20 | chr5 | 74762650 | ||||||
chr5:74762654
|
T | A | 1 | a0001c0001t0001g0122 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.63+1026A>T | GFM2 | ENSG00000164347.18 | transcript | ENST00000296805.8 | protein_coding | 2/20 | chr5 | 74762654 | ||||||
chr5:74762656
|
G | A | 1 | a0001c0001t0001g0122 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.63+1024C>T | GFM2 | ENSG00000164347.18 | transcript | ENST00000296805.8 | protein_coding | 2/20 | chr5 | 74762656 | ||||||
chr5:74762657
|
G | A | 1 | a0001c0001t0001g0122 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.63+1023C>T | GFM2 | ENSG00000164347.18 | transcript | ENST00000296805.8 | protein_coding | 2/20 | chr5 | 74762657 | ||||||
chr5:74762660
|
C | G | 1 | a0001c0001t0001g0122 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.63+1020G>C | GFM2 | ENSG00000164347.18 | transcript | ENST00000296805.8 | protein_coding | 2/20 | chr5 | 74762660 | ||||||
chr5:74762663
|
G | T | 1 | a0001c0001t0001g0122 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.63+1017C>A | GFM2 | ENSG00000164347.18 | transcript | ENST00000296805.8 | protein_coding | 2/20 | chr5 | 74762663 | ||||||
chr5:74762665
|
T | C | 1 | a0001c0001t0001g0122 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.63+1015A>G | GFM2 | ENSG00000164347.18 | transcript | ENST00000296805.8 | protein_coding | 2/20 | chr5 | 74762665 | ||||||
chr5:74762670
|
T | A | 1 | a0001c0001t0001g0122 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.63+1010A>T | GFM2 | ENSG00000164347.18 | transcript | ENST00000296805.8 | protein_coding | 2/20 | chr5 | 74762670 | ||||||
chr5:74762675
|
T | G | 1 | a0001c0001t0001g0122 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.63+1005A>C | GFM2 | ENSG00000164347.18 | transcript | ENST00000296805.8 | protein_coding | 2/20 | chr5 | 74762675 | ||||||
chr5:74762677
|
A | C | 1 | a0001c0001t0001g0122 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.63+1003T>G | GFM2 | ENSG00000164347.18 | transcript | ENST00000296805.8 | protein_coding | 2/20 | chr5 | 74762677 | ||||||
chr5:74762751
|
T | G | 1 | a0001c0001t0001g0122 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.63+929A>C | GFM2 | ENSG00000164347.18 | transcript | ENST00000296805.8 | protein_coding | 2/20 | chr5 | 74762751 | ||||||
chr5:74762752
|
G | T | 1 | a0001c0001t0001g0122 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.63+928C>A | GFM2 | ENSG00000164347.18 | transcript | ENST00000296805.8 | protein_coding | 2/20 | chr5 | 74762752 | ||||||
chr5:74762767
|
T | A | 1 | a0001c0001t0001g0122 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.63+913A>T | GFM2 | ENSG00000164347.18 | transcript | ENST00000296805.8 | protein_coding | 2/20 | chr5 | 74762767 | ||||||
chr5:74762778
|
T | C | 1 | a0002c0002t0001g0243 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.63+902A>G | GFM2 | ENSG00000164347.18 | transcript | ENST00000296805.8 | protein_coding | 2/20 | chr5 | 74762778 | ||||||
chr5:74762788
|
A | G | 134 | a0001c0011t0002g0042a0001c0011t0002g0070a0002c0002t0001g0019others(131): Show | 154 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(151): Show |
intron_variant | MODIFIER | c.63+892T>C | GFM2 | ENSG00000164347.18 | transcript | ENST00000296805.8 | protein_coding | 2/20 | chr5 | 74762788 | ||||||
chr5:74762799
|
T | A | 1 | a0001c0001t0001g0122 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.63+881A>T | GFM2 | ENSG00000164347.18 | transcript | ENST00000296805.8 | protein_coding | 2/20 | chr5 | 74762799 | ||||||
chr5:74762805
|
G | A | 1 | a0001c0001t0001g0122 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.63+875C>T | GFM2 | ENSG00000164347.18 | transcript | ENST00000296805.8 | protein_coding | 2/20 | chr5 | 74762805 | ||||||
chr5:74762807
|
G | A | 1 | a0001c0001t0001g0122 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.63+873C>T | GFM2 | ENSG00000164347.18 | transcript | ENST00000296805.8 | protein_coding | 2/20 | chr5 | 74762807 | ||||||
chr5:74762808
|
G | A | 1 | a0001c0001t0001g0122 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.63+872C>T | GFM2 | ENSG00000164347.18 | transcript | ENST00000296805.8 | protein_coding | 2/20 | chr5 | 74762808 | ||||||
chr5:74762810
|
ATTAAGTG others(4): Show |
A | 1 | a0001c0001t0001g0122 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.63+859_63+869delAT others(9): Show |
GFM2 | ENSG00000164347.18 | transcript | ENST00000296805.8 | protein_coding | 2/20 | chr5 | 74762810 | ||||||
chr5:74762822
|
G | A | 1 | a0001c0001t0001g0122 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.63+858C>T | GFM2 | ENSG00000164347.18 | transcript | ENST00000296805.8 | protein_coding | 2/20 | chr5 | 74762822 | ||||||
chr5:74762829
|
G | A | 1 | a0001c0001t0001g0122 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.63+851C>T | GFM2 | ENSG00000164347.18 | transcript | ENST00000296805.8 | protein_coding | 2/20 | chr5 | 74762829 | ||||||
chr5:74762861
|
T | A | 1 | a0001c0001t0001g0122 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.63+819A>T | GFM2 | ENSG00000164347.18 | transcript | ENST00000296805.8 | protein_coding | 2/20 | chr5 | 74762861 | ||||||
chr5:74762862
|
T | C | 1 | a0001c0001t0001g0122 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.63+818A>G | GFM2 | ENSG00000164347.18 | transcript | ENST00000296805.8 | protein_coding | 2/20 | chr5 | 74762862 | ||||||
chr5:74762863
|
T | A | 1 | a0001c0001t0001g0122 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.63+817A>T | GFM2 | ENSG00000164347.18 | transcript | ENST00000296805.8 | protein_coding | 2/20 | chr5 | 74762863 | ||||||
chr5:74762866
|
A | C | 1 | a0001c0001t0001g0122 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.63+814T>G | GFM2 | ENSG00000164347.18 | transcript | ENST00000296805.8 | protein_coding | 2/20 | chr5 | 74762866 | ||||||
chr5:74762869
|
T | A | 1 | a0001c0001t0001g0122 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.63+811A>T | GFM2 | ENSG00000164347.18 | transcript | ENST00000296805.8 | protein_coding | 2/20 | chr5 | 74762869 | ||||||
chr5:74762870
|
T | C | 1 | a0001c0001t0001g0122 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.63+810A>G | GFM2 | ENSG00000164347.18 | transcript | ENST00000296805.8 | protein_coding | 2/20 | chr5 | 74762870 | ||||||
chr5:74762871
|
ATGAATTA others(25): Show |
A | 1 | a0001c0001t0001g0122 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.63+777_63+808delAA others(30): Show |
GFM2 | ENSG00000164347.18 | transcript | ENST00000296805.8 | protein_coding | 2/20 | chr5 | 74762871 | ||||||
chr5:74762906
|
G | C | 1 | a0001c0001t0001g0122 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.63+774C>G | GFM2 | ENSG00000164347.18 | transcript | ENST00000296805.8 | protein_coding | 2/20 | chr5 | 74762906 | ||||||
chr5:74762907
|
A | C | 1 | a0001c0001t0001g0122 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.63+773T>G | GFM2 | ENSG00000164347.18 | transcript | ENST00000296805.8 | protein_coding | 2/20 | chr5 | 74762907 | ||||||
chr5:74762910
|
A | C | 1 | a0001c0001t0001g0122 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.63+770T>G | GFM2 | ENSG00000164347.18 | transcript | ENST00000296805.8 | protein_coding | 2/20 | chr5 | 74762910 | ||||||
chr5:74762913
|
G | A | 1 | a0001c0001t0001g0122 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.63+767C>T | GFM2 | ENSG00000164347.18 | transcript | ENST00000296805.8 | protein_coding | 2/20 | chr5 | 74762913 | ||||||
chr5:74762914
|
T | C | 1 | a0001c0001t0001g0122 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.63+766A>G | GFM2 | ENSG00000164347.18 | transcript | ENST00000296805.8 | protein_coding | 2/20 | chr5 | 74762914 | ||||||
chr5:74762915
|
T | A | 1 | a0001c0001t0001g0122 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.63+765A>T | GFM2 | ENSG00000164347.18 | transcript | ENST00000296805.8 | protein_coding | 2/20 | chr5 | 74762915 | ||||||
chr5:74762916
|
G | A | 1 | a0001c0001t0001g0122 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.63+764C>T | GFM2 | ENSG00000164347.18 | transcript | ENST00000296805.8 | protein_coding | 2/20 | chr5 | 74762916 | ||||||
chr5:74762919
|
T | A | 1 | a0001c0001t0001g0122 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.63+761A>T | GFM2 | ENSG00000164347.18 | transcript | ENST00000296805.8 | protein_coding | 2/20 | chr5 | 74762919 | ||||||
chr5:74762921
|
T | C | 1 | a0001c0001t0001g0122 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.63+759A>G | GFM2 | ENSG00000164347.18 | transcript | ENST00000296805.8 | protein_coding | 2/20 | chr5 | 74762921 | ||||||
chr5:74762922
|
G | A | 1 | a0001c0001t0001g0122 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.63+758C>T | GFM2 | ENSG00000164347.18 | transcript | ENST00000296805.8 | protein_coding | 2/20 | chr5 | 74762922 | ||||||
chr5:74762924
|
G | A | 1 | a0001c0001t0001g0122 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.63+756C>T | GFM2 | ENSG00000164347.18 | transcript | ENST00000296805.8 | protein_coding | 2/20 | chr5 | 74762924 | ||||||
chr5:74762925
|
C | CCCCCCCC others(37): Show |
1 | a0001c0001t0001g0122 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.63+754_63+755insTG others(42): Show |
GFM2 | ENSG00000164347.18 | transcript | ENST00000296805.8 | protein_coding | 2/20 | chr5 | 74762925 | ||||||
chr5:74763022
|
TTAAAG | T | 85 | a0001c0011t0002g0042a0001c0011t0002g0070a0002c0002t0001g0019others(82): Show | 98 | HG00099.hp2 HG00408.hp2 HG00438.hp2 others(95): Show |
intron_variant | MODIFIER | c.63+653_63+657delCT others(3): Show |
GFM2 | ENSG00000164347.18 | transcript | ENST00000296805.8 | protein_coding | 2/20 | chr5 | 74763022 | ||||||
chr5:74763083
|
T | A | 1 | a0001c0001t0001g0224 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.63+597A>T | GFM2 | ENSG00000164347.18 | transcript | ENST00000296805.8 | protein_coding | 2/20 | chr5 | 74763083 | ||||||
chr5:74763155
|
A | G | 1 | a0001c0001t0003g0252 | 1 | NA19055.hp2 | intron_variant | MODIFIER | c.63+525T>C | GFM2 | ENSG00000164347.18 | transcript | ENST00000296805.8 | protein_coding | 2/20 | chr5 | 74763155 | ||||||
chr5:74763248
|
T | C | 1 | a0001c0001t0001g0086 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.63+432A>G | GFM2 | ENSG00000164347.18 | transcript | ENST00000296805.8 | protein_coding | 2/20 | chr5 | 74763248 | ||||||
chr5:74763266
|
T | C | 35 | a0001c0001t0001g0225a0001c0001t0001g0226a0001c0001t0001g0227others(32): Show | 42 | HG00673.hp1 HG00741.hp1 HG01123.hp2 others(39): Show |
intron_variant | MODIFIER | c.63+414A>G | GFM2 | ENSG00000164347.18 | transcript | ENST00000296805.8 | protein_coding | 2/20 | chr5 | 74763266 | ||||||
chr5:74763269
|
A | G | 2 | a0003c0003t0001g0275a0003c0003t0001g0276 | 2 | HG00738.hp2 HG01361.hp1 |
intron_variant | MODIFIER | c.63+411T>C | GFM2 | ENSG00000164347.18 | transcript | ENST00000296805.8 | protein_coding | 2/20 | chr5 | 74763269 | ||||||
chr5:74763550
|
G | C | 9 | a0002c0005t0001g0034a0002c0005t0001g0040a0002c0005t0001g0244others(6): Show | 11 | HG02145.hp2 HG02451.hp2 HG02559.hp2 others(8): Show |
intron_variant | MODIFIER | c.63+130C>G | GFM2 | ENSG00000164347.18 | transcript | ENST00000296805.8 | protein_coding | 2/20 | chr5 | 74763550 | ||||||
chr5:74763802
|
C | T | 1 | a0002c0002t0001g0237 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.-24-36G>A | GFM2 | ENSG00000164347.18 | transcript | ENST00000296805.8 | protein_coding | 1/20 | chr5 | 74763802 | ||||||
chr5:74763883
|
T | C | 35 | a0003c0003t0001g0011a0003c0003t0001g0012a0003c0003t0001g0038others(32): Show | 42 | HG00140.hp1 HG00280.hp2 HG00642.hp2 others(39): Show |
intron_variant | MODIFIER | c.-24-117A>G | GFM2 | ENSG00000164347.18 | transcript | ENST00000296805.8 | protein_coding | 1/20 | chr5 | 74763883 | ||||||
chr5:74763945
|
T | A | 5 | a0006c0008t0001g0134a0006c0008t0001g0171a0006c0008t0001g0172others(2): Show | 5 | HG00438.hp2 HG00735.hp2 HG02293.hp1 others(2): Show |
intron_variant | MODIFIER | c.-24-179A>T | GFM2 | ENSG00000164347.18 | transcript | ENST00000296805.8 | protein_coding | 1/20 | chr5 | 74763945 | ||||||
chr5:74763990
|
GT | G | 9 | a0002c0005t0001g0034a0002c0005t0001g0040a0002c0005t0001g0244others(6): Show | 11 | HG02145.hp2 HG02451.hp2 HG02559.hp2 others(8): Show |
intron_variant | MODIFIER | c.-24-225delA | GFM2 | ENSG00000164347.18 | transcript | ENST00000296805.8 | protein_coding | 1/20 | chr5 | 74763990 | ||||||
chr5:74764001
|
G | A | 1 | a0009c0012t0001g0299 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.-24-235C>T | GFM2 | ENSG00000164347.18 | transcript | ENST00000296805.8 | protein_coding | 1/20 | chr5 | 74764001 | ||||||
chr5:74764024
|
C | A | 3 | a0001c0001t0001g0003a0001c0001t0001g0094a0001c0001t0001g0125 | 7 | HG01928.hp1 HG01943.hp2 HG01975.hp1 others(4): Show |
intron_variant | MODIFIER | c.-24-258G>T | GFM2 | ENSG00000164347.18 | transcript | ENST00000296805.8 | protein_coding | 1/20 | chr5 | 74764024 | ||||||
chr5:74764026
|
G | A | 35 | a0003c0003t0001g0011a0003c0003t0001g0012a0003c0003t0001g0038others(32): Show | 42 | HG00140.hp1 HG00280.hp2 HG00642.hp2 others(39): Show |
intron_variant | MODIFIER | c.-24-260C>T | GFM2 | ENSG00000164347.18 | transcript | ENST00000296805.8 | protein_coding | 1/20 | chr5 | 74764026 | ||||||
chr5:74764343
|
G | A | 2 | a0002c0005t0001g0231a0002c0005t0001g0232 | 2 | HG01891.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.-24-577C>T | GFM2 | ENSG00000164347.18 | transcript | ENST00000296805.8 | protein_coding | 1/20 | chr5 | 74764343 | ||||||
chr5:74764493
|
T | C | 2 | a0002c0002t0001g0233a0002c0002t0001g0237 | 2 | HG03041.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.-24-727A>G | GFM2 | ENSG00000164347.18 | transcript | ENST00000296805.8 | protein_coding | 1/20 | chr5 | 74764493 | ||||||
chr5:74764500
|
T | A | 12 | a0002c0006t0001g0127a0002c0006t0001g0132a0002c0006t0001g0135others(9): Show | 12 | HG02559.hp1 HG02615.hp2 HG02723.hp2 others(9): Show |
intron_variant | MODIFIER | c.-24-734A>T | GFM2 | ENSG00000164347.18 | transcript | ENST00000296805.8 | protein_coding | 1/20 | chr5 | 74764500 | ||||||
chr5:74764598
|
T | C | 1 | a0007c0010t0001g0234 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.-24-832A>G | GFM2 | ENSG00000164347.18 | transcript | ENST00000296805.8 | protein_coding | 1/20 | chr5 | 74764598 | ||||||
chr5:74764632
|
GTTA | G | 12 | a0002c0006t0001g0127a0002c0006t0001g0132a0002c0006t0001g0135others(9): Show | 12 | HG02559.hp1 HG02615.hp2 HG02723.hp2 others(9): Show |
intron_variant | MODIFIER | c.-24-869_-24-867del others(3): Show |
GFM2 | ENSG00000164347.18 | transcript | ENST00000296805.8 | protein_coding | 1/20 | chr5 | 74764632 | ||||||
chr5:74764657
|
T | C | 1 | a0001c0001t0001g0123 | 1 | NA19080.hp2 | intron_variant | MODIFIER | c.-24-891A>G | GFM2 | ENSG00000164347.18 | transcript | ENST00000296805.8 | protein_coding | 1/20 | chr5 | 74764657 | ||||||
chr5:74764733
|
C | T | 1 | a0002c0006t0001g0135 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.-24-967G>A | GFM2 | ENSG00000164347.18 | transcript | ENST00000296805.8 | protein_coding | 1/20 | chr5 | 74764733 | ||||||
chr5:74764778
|
G | GT | 76 | a0001c0001t0001g0021a0001c0001t0001g0022a0001c0001t0001g0087others(73): Show | 83 | HG00558.hp1 HG00621.hp1 HG00673.hp1 others(80): Show |
intron_variant | MODIFIER | c.-24-1013dupA | GFM2 | ENSG00000164347.18 | transcript | ENST00000296805.8 | protein_coding | 1/20 | chr5 | 74764778 | ||||||
chr5:74764778
|
G | GTT | 9 | a0002c0002t0001g0133a0002c0002t0001g0238a0002c0002t0001g0239others(6): Show | 9 | HG00438.hp2 HG01884.hp2 HG02145.hp2 others(6): Show |
intron_variant | MODIFIER | c.-24-1014_-24-1013d others(4): Show |
GFM2 | ENSG00000164347.18 | transcript | ENST00000296805.8 | protein_coding | 1/20 | chr5 | 74764778 | ||||||
chr5:74764778
|
GT | G | 32 | a0001c0001t0001g0124a0001c0001t0001g0125a0001c0001t0001g0235others(29): Show | 39 | HG00140.hp1 HG00280.hp2 HG00642.hp2 others(36): Show |
intron_variant | MODIFIER | c.-24-1013delA | GFM2 | ENSG00000164347.18 | transcript | ENST00000296805.8 | protein_coding | 1/20 | chr5 | 74764778 | ||||||
chr5:74764807
|
AC | A | 6 | a0002c0002t0001g0238a0002c0002t0001g0239a0002c0002t0001g0240others(3): Show | 6 | HG01884.hp2 HG02280.hp1 HG02647.hp1 others(3): Show |
intron_variant | MODIFIER | c.-24-1042delG | GFM2 | ENSG00000164347.18 | transcript | ENST00000296805.8 | protein_coding | 1/20 | chr5 | 74764807 | ||||||
chr5:74765017
|
C | G | 3 | a0001c0001t0001g0129a0001c0001t0001g0130a0001c0001t0001g0131 | 3 | HG00621.hp1 HG02080.hp2 NA18950.hp2 |
intron_variant | MODIFIER | c.-24-1251G>C | GFM2 | ENSG00000164347.18 | transcript | ENST00000296805.8 | protein_coding | 1/20 | chr5 | 74765017 | ||||||
chr5:74765175
|
CTTT | C | 9 | a0002c0005t0001g0034a0002c0005t0001g0040a0002c0005t0001g0244others(6): Show | 11 | HG02145.hp2 HG02451.hp2 HG02559.hp2 others(8): Show |
intron_variant | MODIFIER | c.-24-1412_-24-1410d others(5): Show |
GFM2 | ENSG00000164347.18 | transcript | ENST00000296805.8 | protein_coding | 1/20 | chr5 | 74765175 | ||||||
chr5:74765256
|
T | G | 28 | a0001c0001t0001g0254a0001c0001t0003g0006a0001c0001t0003g0035others(25): Show | 35 | HG00673.hp1 HG00741.hp1 HG01123.hp2 others(32): Show |
intron_variant | MODIFIER | c.-24-1490A>C | GFM2 | ENSG00000164347.18 | transcript | ENST00000296805.8 | protein_coding | 1/20 | chr5 | 74765256 | ||||||
chr5:74765371
|
A | T | 1 | a0001c0001t0001g0128 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.-25+1567T>A | GFM2 | ENSG00000164347.18 | transcript | ENST00000296805.8 | protein_coding | 1/20 | chr5 | 74765371 | ||||||
chr5:74765419
|
T | C | 29 | a0003c0003t0001g0011a0003c0003t0001g0012a0003c0003t0001g0038others(26): Show | 35 | HG00140.hp1 HG00280.hp2 HG00642.hp2 others(32): Show |
intron_variant | MODIFIER | c.-25+1519A>G | GFM2 | ENSG00000164347.18 | transcript | ENST00000296805.8 | protein_coding | 1/20 | chr5 | 74765419 | ||||||
chr5:74765456
|
G | A | 35 | a0003c0003t0001g0011a0003c0003t0001g0012a0003c0003t0001g0038others(32): Show | 42 | HG00140.hp1 HG00280.hp2 HG00642.hp2 others(39): Show |
intron_variant | MODIFIER | c.-25+1482C>T | GFM2 | ENSG00000164347.18 | transcript | ENST00000296805.8 | protein_coding | 1/20 | chr5 | 74765456 | ||||||
chr5:74765588
|
G | A | 1 | a0001c0001t0001g0300 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.-25+1350C>T | GFM2 | ENSG00000164347.18 | transcript | ENST00000296805.8 | protein_coding | 1/20 | chr5 | 74765588 | ||||||
chr5:74765640
|
C | T | 1 | a0002c0006t0001g0127 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.-25+1298G>A | GFM2 | ENSG00000164347.18 | transcript | ENST00000296805.8 | protein_coding | 1/20 | chr5 | 74765640 | ||||||
chr5:74765692
|
G | A | 1 | a0001c0001t0001g0301 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.-25+1246C>T | GFM2 | ENSG00000164347.18 | transcript | ENST00000296805.8 | protein_coding | 1/20 | chr5 | 74765692 | ||||||
chr5:74765763
|
G | A | 1 | a0002c0002t0001g0302 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.-25+1175C>T | GFM2 | ENSG00000164347.18 | transcript | ENST00000296805.8 | protein_coding | 1/20 | chr5 | 74765763 | ||||||
chr5:74766245
|
G | C | 1 | a0002c0002t0002g0083 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.-25+693C>G | GFM2 | ENSG00000164347.18 | transcript | ENST00000296805.8 | protein_coding | 1/20 | chr5 | 74766245 | ||||||
chr5:74766370
|
A | G | 1 | a0001c0001t0001g0086 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.-25+568T>C | GFM2 | ENSG00000164347.18 | transcript | ENST00000296805.8 | protein_coding | 1/20 | chr5 | 74766370 | ||||||
chr5:74766417
|
C | T | 2 | a0001c0001t0001g0084a0001c0001t0001g0085 | 2 | HG01257.hp1 NA20905.hp1 |
intron_variant | MODIFIER | c.-25+521G>A | GFM2 | ENSG00000164347.18 | transcript | ENST00000296805.8 | protein_coding | 1/20 | chr5 | 74766417 | ||||||
chr5:74766441
|
G | C | 48 | a0001c0011t0002g0042a0001c0011t0002g0070a0002c0002t0002g0002others(45): Show | 57 | HG00099.hp2 HG00408.hp2 HG00558.hp1 others(54): Show |
intron_variant | MODIFIER | c.-25+497C>G | GFM2 | ENSG00000164347.18 | transcript | ENST00000296805.8 | protein_coding | 1/20 | chr5 | 74766441 | ||||||
chr5:74766499
|
C | A | 1 | a0001c0001t0001g0126 | 1 | NA19006.hp1 | intron_variant | MODIFIER | c.-25+439G>T | GFM2 | ENSG00000164347.18 | transcript | ENST00000296805.8 | protein_coding | 1/20 | chr5 | 74766499 | ||||||
chr5:74766533
|
G | T | 48 | a0001c0001t0001g0003a0001c0001t0001g0016a0001c0001t0001g0017others(45): Show | 55 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(52): Show |
intron_variant | MODIFIER | c.-25+405C>A | GFM2 | ENSG00000164347.18 | transcript | ENST00000296805.8 | protein_coding | 1/20 | chr5 | 74766533 | ||||||
chr5:74766633
|
T | TCTTCTTC others(11): Show |
1 | a0001c0001t0001g0303 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.-25+287_-25+304dup others(18): Show |
GFM2 | ENSG00000164347.18 | transcript | ENST00000296805.8 | protein_coding | 1/20 | chr5 | 74766633 | ||||||
chr5:74766744
|
G | C | 1 | a0001c0001t0001g0304 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.-25+194C>G | GFM2 | ENSG00000164347.18 | transcript | ENST00000296805.8 | protein_coding | 1/20 | chr5 | 74766744 | ||||||
chr5:74766771
|
T | G | 1 | a0001c0001t0001g0305 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.-25+167A>C | GFM2 | ENSG00000164347.18 | transcript | ENST00000296805.8 | protein_coding | 1/20 | chr5 | 74766771 | ||||||
chr5:74766774
|
T | C | 6 | a0002c0005t0001g0040a0002c0005t0001g0306a0002c0005t0001g0307others(3): Show | 7 | HG02145.hp2 HG02559.hp2 HG02723.hp1 others(4): Show |
intron_variant | MODIFIER | c.-25+164A>G | GFM2 | ENSG00000164347.18 | transcript | ENST00000296805.8 | protein_coding | 1/20 | chr5 | 74766774 |