geneid | 85476 |
---|---|
ensemblid | ENSG00000168827.15 |
hgncid | 13780 |
symbol | GFM1 |
name | G elongation factor mitochondrial 1 |
refseq_nuc | NM_024996.7 |
refseq_prot | NP_079272.4 |
ensembl_nuc | ENST00000486715.6 |
ensembl_prot | ENSP00000419038.1 |
mane_status | MANE Select |
chr | chr3 |
start | 158644527 |
end | 158695581 |
strand | + |
ver | v1.2 |
region | chr3:158644527-158695581 |
region5000 | chr3:158639527-158700581 |
regionname0 | GFM1_chr3_158644527_158695581 |
regionname5000 | GFM1_chr3_158639527_158700581 |
ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 0/0 | 751 | 219 | 68 | 32 | 88 | 11 | 20 | 71 | GFM1_chr3_158639527_158700581 | GFM1 | copy fasta | chr3 | 158639527 | 158700581 |
a0002 | 1/1 | 751 | 136 | 13 | 27 | 70 | 7 | 17 | 56 | GFM1_chr3_158639527_158700581 | GFM1 | copy fasta | chr3 | 158639527 | 158700581 |
a0003 | 0/0 | 751 | 7 | 6 | 1 | 0 | 0 | 0 | 0 | GFM1_chr3_158639527_158700581 | GFM1 | copy fasta | chr3 | 158639527 | 158700581 |
a0004 | 0/0 | 751 | 3 | 0 | 0 | 3 | 0 | 0 | 3 | GFM1_chr3_158639527_158700581 | GFM1 | copy fasta | chr3 | 158639527 | 158700581 |
a0005 | 0/0 | 38 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | GFM1_chr3_158639527_158700581 | GFM1 | copy fasta | chr3 | 158639527 | 158700581 |
a0006 | 0/0 | 751 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | GFM1_chr3_158639527_158700581 | GFM1 | copy fasta | chr3 | 158639527 | 158700581 |
a0007 | 0/0 | 751 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | GFM1_chr3_158639527_158700581 | GFM1 | copy fasta | chr3 | 158639527 | 158700581 |
a0008 | 0/0 | 751 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | GFM1_chr3_158639527_158700581 | GFM1 | copy fasta | chr3 | 158639527 | 158700581 |
a0009 | 0/0 | 751 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | GFM1_chr3_158639527_158700581 | GFM1 | copy fasta | chr3 | 158639527 | 158700581 |
a0010 | 0/0 | 751 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | GFM1_chr3_158639527_158700581 | GFM1 | copy fasta | chr3 | 158639527 | 158700581 |
a0011 | 0/0 | 751 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | GFM1_chr3_158639527_158700581 | GFM1 | copy fasta | chr3 | 158639527 | 158700581 |
chapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
c0001 | 0/0 | 2256 | 214 | 65 | 31 | 87 | 11 | 20 | GFM1_chr3_158639527_158700581 | GFM1 | copy fasta | chr3 | 158639527 | 158700581 |
c0002 | 1/1 | 2256 | 135 | 13 | 27 | 69 | 7 | 17 | GFM1_chr3_158639527_158700581 | GFM1 | copy fasta | chr3 | 158639527 | 158700581 |
c0003 | 0/0 | 2256 | 7 | 6 | 1 | 0 | 0 | 0 | GFM1_chr3_158639527_158700581 | GFM1 | copy fasta | chr3 | 158639527 | 158700581 |
c0004 | 0/0 | 2256 | 3 | 1 | 1 | 1 | 0 | 0 | GFM1_chr3_158639527_158700581 | GFM1 | copy fasta | chr3 | 158639527 | 158700581 |
c0005 | 0/0 | 2256 | 3 | 0 | 0 | 3 | 0 | 0 | GFM1_chr3_158639527_158700581 | GFM1 | copy fasta | chr3 | 158639527 | 158700581 |
c0006 | 0/0 | 2245 | 1 | 1 | 0 | 0 | 0 | 0 | GFM1_chr3_158639527_158700581 | GFM1 | copy fasta | chr3 | 158639527 | 158700581 |
c0007 | 0/0 | 2256 | 1 | 0 | 1 | 0 | 0 | 0 | GFM1_chr3_158639527_158700581 | GFM1 | copy fasta | chr3 | 158639527 | 158700581 |
c0008 | 0/0 | 2256 | 1 | 1 | 0 | 0 | 0 | 0 | GFM1_chr3_158639527_158700581 | GFM1 | copy fasta | chr3 | 158639527 | 158700581 |
c0009 | 0/0 | 2256 | 1 | 1 | 0 | 0 | 0 | 0 | GFM1_chr3_158639527_158700581 | GFM1 | copy fasta | chr3 | 158639527 | 158700581 |
c0010 | 0/0 | 2256 | 1 | 1 | 0 | 0 | 0 | 0 | GFM1_chr3_158639527_158700581 | GFM1 | copy fasta | chr3 | 158639527 | 158700581 |
c0011 | 0/0 | 2256 | 1 | 0 | 0 | 0 | 0 | 1 | GFM1_chr3_158639527_158700581 | GFM1 | copy fasta | chr3 | 158639527 | 158700581 |
c0012 | 0/0 | 2256 | 1 | 0 | 0 | 1 | 0 | 0 | GFM1_chr3_158639527_158700581 | GFM1 | copy fasta | chr3 | 158639527 | 158700581 |
c0013 | 0/0 | 2256 | 1 | 0 | 0 | 1 | 0 | 0 | GFM1_chr3_158639527_158700581 | GFM1 | copy fasta | chr3 | 158639527 | 158700581 |
c0014 | 0/0 | 2256 | 1 | 1 | 0 | 0 | 0 | 0 | GFM1_chr3_158639527_158700581 | GFM1 | copy fasta | chr3 | 158639527 | 158700581 |
c0015 | 0/0 | 2256 | 1 | 0 | 1 | 0 | 0 | 0 | GFM1_chr3_158639527_158700581 | GFM1 | copy fasta | chr3 | 158639527 | 158700581 |
thapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
t0001 | 0/1 | 4223 | 130 | 14 | 26 | 67 | 6 | 16 | GFM1_chr3_158639527_158700581 | GFM1 | copy fasta | chr3 | 158639527 | 158700581 |
t0002 | 0/0 | 4223 | 56 | 5 | 9 | 32 | 4 | 6 | GFM1_chr3_158639527_158700581 | GFM1 | copy fasta | chr3 | 158639527 | 158700581 |
t0003 | 0/0 | 4219 | 54 | 8 | 10 | 30 | 3 | 3 | GFM1_chr3_158639527_158700581 | GFM1 | copy fasta | chr3 | 158639527 | 158700581 |
t0004 | 0/0 | 4223 | 52 | 18 | 10 | 12 | 4 | 8 | GFM1_chr3_158639527_158700581 | GFM1 | copy fasta | chr3 | 158639527 | 158700581 |
t0005 | 0/0 | 4221 | 9 | 9 | 0 | 0 | 0 | 0 | GFM1_chr3_158639527_158700581 | GFM1 | copy fasta | chr3 | 158639527 | 158700581 |
t0006 | 0/0 | 4223 | 9 | 0 | 0 | 9 | 0 | 0 | GFM1_chr3_158639527_158700581 | GFM1 | copy fasta | chr3 | 158639527 | 158700581 |
t0007 | 0/0 | 4223 | 8 | 7 | 1 | 0 | 0 | 0 | GFM1_chr3_158639527_158700581 | GFM1 | copy fasta | chr3 | 158639527 | 158700581 |
t0008 | 0/0 | 4223 | 6 | 6 | 0 | 0 | 0 | 0 | GFM1_chr3_158639527_158700581 | GFM1 | copy fasta | chr3 | 158639527 | 158700581 |
t0009 | 0/0 | 4223 | 5 | 5 | 0 | 0 | 0 | 0 | GFM1_chr3_158639527_158700581 | GFM1 | copy fasta | chr3 | 158639527 | 158700581 |
t0010 | 1/0 | 4223 | 4 | 0 | 2 | 0 | 1 | 0 | GFM1_chr3_158639527_158700581 | GFM1 | copy fasta | chr3 | 158639527 | 158700581 |
t0011 | 0/0 | 4223 | 4 | 4 | 0 | 0 | 0 | 0 | GFM1_chr3_158639527_158700581 | GFM1 | copy fasta | chr3 | 158639527 | 158700581 |
t0012 | 0/0 | 4223 | 3 | 0 | 0 | 3 | 0 | 0 | GFM1_chr3_158639527_158700581 | GFM1 | copy fasta | chr3 | 158639527 | 158700581 |
t0013 | 0/0 | 4223 | 3 | 0 | 0 | 3 | 0 | 0 | GFM1_chr3_158639527_158700581 | GFM1 | copy fasta | chr3 | 158639527 | 158700581 |
t0014 | 0/0 | 4223 | 3 | 3 | 0 | 0 | 0 | 0 | GFM1_chr3_158639527_158700581 | GFM1 | copy fasta | chr3 | 158639527 | 158700581 |
t0015 | 0/0 | 4223 | 2 | 0 | 0 | 0 | 0 | 2 | GFM1_chr3_158639527_158700581 | GFM1 | copy fasta | chr3 | 158639527 | 158700581 |
t0016 | 0/0 | 4223 | 2 | 2 | 0 | 0 | 0 | 0 | GFM1_chr3_158639527_158700581 | GFM1 | copy fasta | chr3 | 158639527 | 158700581 |
t0017 | 0/0 | 4223 | 2 | 2 | 0 | 0 | 0 | 0 | GFM1_chr3_158639527_158700581 | GFM1 | copy fasta | chr3 | 158639527 | 158700581 |
t0018 | 0/0 | 4223 | 2 | 2 | 0 | 0 | 0 | 0 | GFM1_chr3_158639527_158700581 | GFM1 | copy fasta | chr3 | 158639527 | 158700581 |
t0019 | 0/0 | 4223 | 1 | 0 | 0 | 1 | 0 | 0 | GFM1_chr3_158639527_158700581 | GFM1 | copy fasta | chr3 | 158639527 | 158700581 |
t0020 | 0/0 | 4223 | 1 | 0 | 0 | 1 | 0 | 0 | GFM1_chr3_158639527_158700581 | GFM1 | copy fasta | chr3 | 158639527 | 158700581 |
t0021 | 0/0 | 4223 | 1 | 0 | 0 | 1 | 0 | 0 | GFM1_chr3_158639527_158700581 | GFM1 | copy fasta | chr3 | 158639527 | 158700581 |
t0022 | 0/0 | 4223 | 1 | 0 | 0 | 0 | 0 | 1 | GFM1_chr3_158639527_158700581 | GFM1 | copy fasta | chr3 | 158639527 | 158700581 |
t0023 | 0/0 | 4223 | 1 | 1 | 0 | 0 | 0 | 0 | GFM1_chr3_158639527_158700581 | GFM1 | copy fasta | chr3 | 158639527 | 158700581 |
t0024 | 0/0 | 4223 | 1 | 0 | 0 | 1 | 0 | 0 | GFM1_chr3_158639527_158700581 | GFM1 | copy fasta | chr3 | 158639527 | 158700581 |
t0025 | 0/0 | 4223 | 1 | 1 | 0 | 0 | 0 | 0 | GFM1_chr3_158639527_158700581 | GFM1 | copy fasta | chr3 | 158639527 | 158700581 |
t0026 | 0/0 | 4223 | 1 | 0 | 1 | 0 | 0 | 0 | GFM1_chr3_158639527_158700581 | GFM1 | copy fasta | chr3 | 158639527 | 158700581 |
t0027 | 0/0 | 4223 | 1 | 0 | 1 | 0 | 0 | 0 | GFM1_chr3_158639527_158700581 | GFM1 | copy fasta | chr3 | 158639527 | 158700581 |
t0028 | 0/0 | 4223 | 1 | 0 | 1 | 0 | 0 | 0 | GFM1_chr3_158639527_158700581 | GFM1 | copy fasta | chr3 | 158639527 | 158700581 |
t0029 | 0/0 | 4223 | 1 | 1 | 0 | 0 | 0 | 0 | GFM1_chr3_158639527_158700581 | GFM1 | copy fasta | chr3 | 158639527 | 158700581 |
t0030 | 0/0 | 4223 | 1 | 1 | 0 | 0 | 0 | 0 | GFM1_chr3_158639527_158700581 | GFM1 | copy fasta | chr3 | 158639527 | 158700581 |
t0031 | 0/0 | 4223 | 1 | 0 | 0 | 0 | 0 | 1 | GFM1_chr3_158639527_158700581 | GFM1 | copy fasta | chr3 | 158639527 | 158700581 |
t0032 | 0/0 | 4219 | 1 | 0 | 0 | 1 | 0 | 0 | GFM1_chr3_158639527_158700581 | GFM1 | copy fasta | chr3 | 158639527 | 158700581 |
t0033 | 0/0 | 4219 | 1 | 0 | 0 | 1 | 0 | 0 | GFM1_chr3_158639527_158700581 | GFM1 | copy fasta | chr3 | 158639527 | 158700581 |
t0034 | 0/0 | 4219 | 1 | 0 | 1 | 0 | 0 | 0 | GFM1_chr3_158639527_158700581 | GFM1 | copy fasta | chr3 | 158639527 | 158700581 |
t0035 | 0/0 | 4223 | 1 | 0 | 0 | 0 | 0 | 1 | GFM1_chr3_158639527_158700581 | GFM1 | copy fasta | chr3 | 158639527 | 158700581 |
t0036 | 0/0 | 4223 | 1 | 1 | 0 | 0 | 0 | 0 | GFM1_chr3_158639527_158700581 | GFM1 | copy fasta | chr3 | 158639527 | 158700581 |
ghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
g0001 | 0/0 | 11 | 1 | 3 | 6 | 1 | 0 | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
g0002 | 0/0 | 8 | 0 | 4 | 3 | 0 | 1 | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
g0003 | 0/0 | 5 | 2 | 0 | 2 | 0 | 1 | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
g0004 | 0/0 | 5 | 0 | 3 | 0 | 0 | 2 | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
g0005 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
g0006 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
g0007 | 0/0 | 4 | 0 | 1 | 0 | 1 | 2 | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
g0008 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
g0009 | 0/0 | 4 | 1 | 1 | 2 | 0 | 0 | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
g0010 | 0/0 | 3 | 0 | 0 | 0 | 2 | 1 | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
g0011 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
g0012 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
g0013 | 0/0 | 3 | 0 | 1 | 1 | 0 | 1 | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
g0014 | 0/0 | 3 | 0 | 1 | 1 | 1 | 0 | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
g0015 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
g0016 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
g0017 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
g0018 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
g0019 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
g0020 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
g0021 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
g0022 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
g0023 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
g0024 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
g0025 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
g0026 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
g0027 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
g0028 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
g0029 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
g0030 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
g0031 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
g0032 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
g0033 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
g0034 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
g0035 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
g0037 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
g0041 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
g0042 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
g0049 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
g0052 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
g0053 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
g0056 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
g0058 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
g0066 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
g0067 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
g0070 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
g0083 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
g0086 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
g0089 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
g0092 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
g0093 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
g0106 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
g0107 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
g0108 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
g0109 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
g0111 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
g0112 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
g0122 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
g0123 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
g0124 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
g0125 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
g0126 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
g0127 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
g0130 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
g0131 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
g0132 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
g0137 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
g0138 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
g0139 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
g0140 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
g0143 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
g0145 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
g0146 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
g0147 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
g0149 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
g0154 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
g0156 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
g0158 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
g0171 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
g0182 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
g0183 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
g0184 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
g0188 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
g0189 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
g0196 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
g0199 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
g0200 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
g0202 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
g0203 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
g0215 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
g0220 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
g0221 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
g0222 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
g0230 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
g0236 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
g0238 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
g0241 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
g0242 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
g0243 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
g0246 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
g0247 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
g0248 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
g0249 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
g0251 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
g0252 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
g0253 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
g0254 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
g0255 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
g0256 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
g0257 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
g0258 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
g0260 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
g0261 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
g0262 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
g0263 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
g0264 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
g0265 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
g0266 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
g0267 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
g0268 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
g0269 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
g0270 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
g0271 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
g0272 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
g0274 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
g0276 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
g0277 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
g0278 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
g0279 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
g0280 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
g0281 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
g0282 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
g0284 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
g0285 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
g0286 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
g0287 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
g0288 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
g0289 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
g0290 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
g0291 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
g0292 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
g0293 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
g0294 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
g0295 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
g0296 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
g0298 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
g0299 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
g0300 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
g0302 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
g0303 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
g0304 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
g0305 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
g0306 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
achapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 0/0 | 2256 | 214 | 65 | 31 | 87 | 11 | 20 | GFM1_chr3_158639527_158700581 | GFM1 | copy fasta | chr3 | 158639527 | 158700581 |
a0001c0004 | 0/0 | 2256 | 3 | 1 | 1 | 1 | 0 | 0 | GFM1_chr3_158639527_158700581 | GFM1 | copy fasta | chr3 | 158639527 | 158700581 |
a0001c0008 | 0/0 | 2256 | 1 | 1 | 0 | 0 | 0 | 0 | GFM1_chr3_158639527_158700581 | GFM1 | copy fasta | chr3 | 158639527 | 158700581 |
a0001c0009 | 0/0 | 2256 | 1 | 1 | 0 | 0 | 0 | 0 | GFM1_chr3_158639527_158700581 | GFM1 | copy fasta | chr3 | 158639527 | 158700581 |
a0002c0002 | 1/1 | 2256 | 135 | 13 | 27 | 69 | 7 | 17 | GFM1_chr3_158639527_158700581 | GFM1 | copy fasta | chr3 | 158639527 | 158700581 |
a0002c0013 | 0/0 | 2256 | 1 | 0 | 0 | 1 | 0 | 0 | GFM1_chr3_158639527_158700581 | GFM1 | copy fasta | chr3 | 158639527 | 158700581 |
a0003c0003 | 0/0 | 2256 | 7 | 6 | 1 | 0 | 0 | 0 | GFM1_chr3_158639527_158700581 | GFM1 | copy fasta | chr3 | 158639527 | 158700581 |
a0004c0005 | 0/0 | 2256 | 3 | 0 | 0 | 3 | 0 | 0 | GFM1_chr3_158639527_158700581 | GFM1 | copy fasta | chr3 | 158639527 | 158700581 |
a0005c0006 | 0/0 | 2245 | 1 | 1 | 0 | 0 | 0 | 0 | GFM1_chr3_158639527_158700581 | GFM1 | copy fasta | chr3 | 158639527 | 158700581 |
a0006c0015 | 0/0 | 2256 | 1 | 0 | 1 | 0 | 0 | 0 | GFM1_chr3_158639527_158700581 | GFM1 | copy fasta | chr3 | 158639527 | 158700581 |
a0007c0010 | 0/0 | 2256 | 1 | 1 | 0 | 0 | 0 | 0 | GFM1_chr3_158639527_158700581 | GFM1 | copy fasta | chr3 | 158639527 | 158700581 |
a0008c0007 | 0/0 | 2256 | 1 | 0 | 1 | 0 | 0 | 0 | GFM1_chr3_158639527_158700581 | GFM1 | copy fasta | chr3 | 158639527 | 158700581 |
a0009c0014 | 0/0 | 2256 | 1 | 1 | 0 | 0 | 0 | 0 | GFM1_chr3_158639527_158700581 | GFM1 | copy fasta | chr3 | 158639527 | 158700581 |
a0010c0012 | 0/0 | 2256 | 1 | 0 | 0 | 1 | 0 | 0 | GFM1_chr3_158639527_158700581 | GFM1 | copy fasta | chr3 | 158639527 | 158700581 |
a0011c0011 | 0/0 | 2256 | 1 | 0 | 0 | 0 | 0 | 1 | GFM1_chr3_158639527_158700581 | GFM1 | copy fasta | chr3 | 158639527 | 158700581 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0002 | 0/0 | 6478 | 54 | 4 | 8 | 32 | 4 | 6 | GFM1_chr3_158639527_158700581 | GFM1 | copy fasta | chr3 | 158639527 | 158700581 |
a0001c0001t0003 | 0/0 | 6474 | 52 | 8 | 10 | 28 | 3 | 3 | GFM1_chr3_158639527_158700581 | GFM1 | copy fasta | chr3 | 158639527 | 158700581 |
a0001c0001t0004 | 0/0 | 6478 | 51 | 18 | 10 | 12 | 4 | 7 | GFM1_chr3_158639527_158700581 | GFM1 | copy fasta | chr3 | 158639527 | 158700581 |
a0001c0001t0005 | 0/0 | 6476 | 9 | 9 | 0 | 0 | 0 | 0 | GFM1_chr3_158639527_158700581 | GFM1 | copy fasta | chr3 | 158639527 | 158700581 |
a0001c0001t0006 | 0/0 | 6478 | 9 | 0 | 0 | 9 | 0 | 0 | GFM1_chr3_158639527_158700581 | GFM1 | copy fasta | chr3 | 158639527 | 158700581 |
a0001c0001t0007 | 0/0 | 6478 | 1 | 1 | 0 | 0 | 0 | 0 | GFM1_chr3_158639527_158700581 | GFM1 | copy fasta | chr3 | 158639527 | 158700581 |
a0001c0001t0008 | 0/0 | 6478 | 5 | 5 | 0 | 0 | 0 | 0 | GFM1_chr3_158639527_158700581 | GFM1 | copy fasta | chr3 | 158639527 | 158700581 |
a0001c0001t0009 | 0/0 | 6478 | 5 | 5 | 0 | 0 | 0 | 0 | GFM1_chr3_158639527_158700581 | GFM1 | copy fasta | chr3 | 158639527 | 158700581 |
a0001c0001t0011 | 0/0 | 6478 | 3 | 3 | 0 | 0 | 0 | 0 | GFM1_chr3_158639527_158700581 | GFM1 | copy fasta | chr3 | 158639527 | 158700581 |
a0001c0001t0013 | 0/0 | 6478 | 3 | 0 | 0 | 3 | 0 | 0 | GFM1_chr3_158639527_158700581 | GFM1 | copy fasta | chr3 | 158639527 | 158700581 |
a0001c0001t0014 | 0/0 | 6478 | 3 | 3 | 0 | 0 | 0 | 0 | GFM1_chr3_158639527_158700581 | GFM1 | copy fasta | chr3 | 158639527 | 158700581 |
a0001c0001t0015 | 0/0 | 6478 | 2 | 0 | 0 | 0 | 0 | 2 | GFM1_chr3_158639527_158700581 | GFM1 | copy fasta | chr3 | 158639527 | 158700581 |
a0001c0001t0016 | 0/0 | 6478 | 2 | 2 | 0 | 0 | 0 | 0 | GFM1_chr3_158639527_158700581 | GFM1 | copy fasta | chr3 | 158639527 | 158700581 |
a0001c0001t0017 | 0/0 | 6478 | 2 | 2 | 0 | 0 | 0 | 0 | GFM1_chr3_158639527_158700581 | GFM1 | copy fasta | chr3 | 158639527 | 158700581 |
a0001c0001t0018 | 0/0 | 6478 | 2 | 2 | 0 | 0 | 0 | 0 | GFM1_chr3_158639527_158700581 | GFM1 | copy fasta | chr3 | 158639527 | 158700581 |
a0001c0001t0020 | 0/0 | 6478 | 1 | 0 | 0 | 1 | 0 | 0 | GFM1_chr3_158639527_158700581 | GFM1 | copy fasta | chr3 | 158639527 | 158700581 |
a0001c0001t0021 | 0/0 | 6478 | 1 | 0 | 0 | 1 | 0 | 0 | GFM1_chr3_158639527_158700581 | GFM1 | copy fasta | chr3 | 158639527 | 158700581 |
a0001c0001t0022 | 0/0 | 6478 | 1 | 0 | 0 | 0 | 0 | 1 | GFM1_chr3_158639527_158700581 | GFM1 | copy fasta | chr3 | 158639527 | 158700581 |
a0001c0001t0023 | 0/0 | 6478 | 1 | 1 | 0 | 0 | 0 | 0 | GFM1_chr3_158639527_158700581 | GFM1 | copy fasta | chr3 | 158639527 | 158700581 |
a0001c0001t0027 | 0/0 | 6478 | 1 | 0 | 1 | 0 | 0 | 0 | GFM1_chr3_158639527_158700581 | GFM1 | copy fasta | chr3 | 158639527 | 158700581 |
a0001c0001t0028 | 0/0 | 6478 | 1 | 0 | 1 | 0 | 0 | 0 | GFM1_chr3_158639527_158700581 | GFM1 | copy fasta | chr3 | 158639527 | 158700581 |
a0001c0001t0030 | 0/0 | 6478 | 1 | 1 | 0 | 0 | 0 | 0 | GFM1_chr3_158639527_158700581 | GFM1 | copy fasta | chr3 | 158639527 | 158700581 |
a0001c0001t0031 | 0/0 | 6478 | 1 | 0 | 0 | 0 | 0 | 1 | GFM1_chr3_158639527_158700581 | GFM1 | copy fasta | chr3 | 158639527 | 158700581 |
a0001c0001t0032 | 0/0 | 6474 | 1 | 0 | 0 | 1 | 0 | 0 | GFM1_chr3_158639527_158700581 | GFM1 | copy fasta | chr3 | 158639527 | 158700581 |
a0001c0001t0034 | 0/0 | 6474 | 1 | 0 | 1 | 0 | 0 | 0 | GFM1_chr3_158639527_158700581 | GFM1 | copy fasta | chr3 | 158639527 | 158700581 |
a0001c0001t0036 | 0/0 | 6478 | 1 | 1 | 0 | 0 | 0 | 0 | GFM1_chr3_158639527_158700581 | GFM1 | copy fasta | chr3 | 158639527 | 158700581 |
a0001c0004t0024 | 0/0 | 6478 | 1 | 0 | 0 | 1 | 0 | 0 | GFM1_chr3_158639527_158700581 | GFM1 | copy fasta | chr3 | 158639527 | 158700581 |
a0001c0004t0025 | 0/0 | 6478 | 1 | 1 | 0 | 0 | 0 | 0 | GFM1_chr3_158639527_158700581 | GFM1 | copy fasta | chr3 | 158639527 | 158700581 |
a0001c0004t0026 | 0/0 | 6478 | 1 | 0 | 1 | 0 | 0 | 0 | GFM1_chr3_158639527_158700581 | GFM1 | copy fasta | chr3 | 158639527 | 158700581 |
a0001c0008t0008 | 0/0 | 6478 | 1 | 1 | 0 | 0 | 0 | 0 | GFM1_chr3_158639527_158700581 | GFM1 | copy fasta | chr3 | 158639527 | 158700581 |
a0001c0009t0029 | 0/0 | 6478 | 1 | 1 | 0 | 0 | 0 | 0 | GFM1_chr3_158639527_158700581 | GFM1 | copy fasta | chr3 | 158639527 | 158700581 |
a0002c0002t0001 | 0/1 | 6478 | 126 | 13 | 25 | 65 | 6 | 16 | GFM1_chr3_158639527_158700581 | GFM1 | copy fasta | chr3 | 158639527 | 158700581 |
a0002c0002t0010 | 1/0 | 6478 | 4 | 0 | 2 | 0 | 1 | 0 | GFM1_chr3_158639527_158700581 | GFM1 | copy fasta | chr3 | 158639527 | 158700581 |
a0002c0002t0012 | 0/0 | 6478 | 3 | 0 | 0 | 3 | 0 | 0 | GFM1_chr3_158639527_158700581 | GFM1 | copy fasta | chr3 | 158639527 | 158700581 |
a0002c0002t0019 | 0/0 | 6478 | 1 | 0 | 0 | 1 | 0 | 0 | GFM1_chr3_158639527_158700581 | GFM1 | copy fasta | chr3 | 158639527 | 158700581 |
a0002c0002t0035 | 0/0 | 6478 | 1 | 0 | 0 | 0 | 0 | 1 | GFM1_chr3_158639527_158700581 | GFM1 | copy fasta | chr3 | 158639527 | 158700581 |
a0002c0013t0001 | 0/0 | 6478 | 1 | 0 | 0 | 1 | 0 | 0 | GFM1_chr3_158639527_158700581 | GFM1 | copy fasta | chr3 | 158639527 | 158700581 |
a0003c0003t0007 | 0/0 | 6478 | 7 | 6 | 1 | 0 | 0 | 0 | GFM1_chr3_158639527_158700581 | GFM1 | copy fasta | chr3 | 158639527 | 158700581 |
a0004c0005t0003 | 0/0 | 6474 | 2 | 0 | 0 | 2 | 0 | 0 | GFM1_chr3_158639527_158700581 | GFM1 | copy fasta | chr3 | 158639527 | 158700581 |
a0004c0005t0033 | 0/0 | 6474 | 1 | 0 | 0 | 1 | 0 | 0 | GFM1_chr3_158639527_158700581 | GFM1 | copy fasta | chr3 | 158639527 | 158700581 |
a0005c0006t0011 | 0/0 | 6467 | 1 | 1 | 0 | 0 | 0 | 0 | GFM1_chr3_158639527_158700581 | GFM1 | copy fasta | chr3 | 158639527 | 158700581 |
a0006c0015t0001 | 0/0 | 6478 | 1 | 0 | 1 | 0 | 0 | 0 | GFM1_chr3_158639527_158700581 | GFM1 | copy fasta | chr3 | 158639527 | 158700581 |
a0007c0010t0002 | 0/0 | 6478 | 1 | 1 | 0 | 0 | 0 | 0 | GFM1_chr3_158639527_158700581 | GFM1 | copy fasta | chr3 | 158639527 | 158700581 |
a0008c0007t0002 | 0/0 | 6478 | 1 | 0 | 1 | 0 | 0 | 0 | GFM1_chr3_158639527_158700581 | GFM1 | copy fasta | chr3 | 158639527 | 158700581 |
a0009c0014t0001 | 0/0 | 6478 | 1 | 1 | 0 | 0 | 0 | 0 | GFM1_chr3_158639527_158700581 | GFM1 | copy fasta | chr3 | 158639527 | 158700581 |
a0010c0012t0001 | 0/0 | 6478 | 1 | 0 | 0 | 1 | 0 | 0 | GFM1_chr3_158639527_158700581 | GFM1 | copy fasta | chr3 | 158639527 | 158700581 |
a0011c0011t0004 | 0/0 | 6478 | 1 | 0 | 0 | 0 | 0 | 1 | GFM1_chr3_158639527_158700581 | GFM1 | copy fasta | chr3 | 158639527 | 158700581 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0002g0001 | 0/0 | 6 | 1 | 3 | 1 | 1 | 0 | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
a0001c0001t0002g0005 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
a0001c0001t0002g0015 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
a0001c0001t0002g0031 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
a0001c0001t0002g0032 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
a0001c0001t0002g0034 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
a0001c0001t0002g0035 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
a0001c0001t0002g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
a0001c0001t0002g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
a0001c0001t0002g0041 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
a0001c0001t0002g0042 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
a0001c0001t0002g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
a0001c0001t0002g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
a0001c0001t0002g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
a0001c0001t0002g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
a0001c0001t0002g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
a0001c0001t0002g0049 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
a0001c0001t0002g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
a0001c0001t0002g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
a0001c0001t0002g0052 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
a0001c0001t0002g0053 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
a0001c0001t0002g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
a0001c0001t0002g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
a0001c0001t0002g0058 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
a0001c0001t0002g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
a0001c0001t0002g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
a0001c0001t0002g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
a0001c0001t0002g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
a0001c0001t0002g0066 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
a0001c0001t0002g0067 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
a0001c0001t0002g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
a0001c0001t0002g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
a0001c0001t0002g0070 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
a0001c0001t0002g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
a0001c0001t0002g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
a0001c0001t0002g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
a0001c0001t0002g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
a0001c0001t0002g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
a0001c0001t0002g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
a0001c0001t0002g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
a0001c0001t0002g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
a0001c0001t0002g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
a0001c0001t0002g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
a0001c0001t0002g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
a0001c0001t0002g0089 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
a0001c0001t0003g0009 | 0/0 | 3 | 1 | 1 | 1 | 0 | 0 | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
a0001c0001t0003g0012 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
a0001c0001t0003g0026 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
a0001c0001t0003g0027 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
a0001c0001t0003g0183 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
a0001c0001t0003g0184 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
a0001c0001t0003g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
a0001c0001t0003g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
a0001c0001t0003g0188 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
a0001c0001t0003g0189 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
a0001c0001t0003g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
a0001c0001t0003g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
a0001c0001t0003g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
a0001c0001t0003g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
a0001c0001t0003g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
a0001c0001t0003g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
a0001c0001t0003g0196 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
a0001c0001t0003g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
a0001c0001t0003g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
a0001c0001t0003g0199 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
a0001c0001t0003g0200 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
a0001c0001t0003g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
a0001c0001t0003g0202 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
a0001c0001t0003g0203 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
a0001c0001t0003g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
a0001c0001t0003g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
a0001c0001t0003g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
a0001c0001t0003g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
a0001c0001t0003g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
a0001c0001t0003g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
a0001c0001t0003g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
a0001c0001t0003g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
a0001c0001t0003g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
a0001c0001t0003g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
a0001c0001t0003g0215 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
a0001c0001t0003g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
a0001c0001t0003g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
a0001c0001t0003g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
a0001c0001t0003g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
a0001c0001t0003g0220 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
a0001c0001t0003g0221 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
a0001c0001t0003g0222 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
a0001c0001t0003g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
a0001c0001t0003g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
a0001c0001t0003g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
a0001c0001t0003g0302 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
a0001c0001t0004g0002 | 0/0 | 7 | 0 | 4 | 2 | 0 | 1 | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
a0001c0001t0004g0013 | 0/0 | 3 | 0 | 1 | 1 | 0 | 1 | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
a0001c0001t0004g0014 | 0/0 | 3 | 0 | 1 | 1 | 1 | 0 | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
a0001c0001t0004g0029 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
a0001c0001t0004g0030 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
a0001c0001t0004g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
a0001c0001t0004g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
a0001c0001t0004g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
a0001c0001t0004g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
a0001c0001t0004g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
a0001c0001t0004g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
a0001c0001t0004g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
a0001c0001t0004g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
a0001c0001t0004g0238 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
a0001c0001t0004g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
a0001c0001t0004g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
a0001c0001t0004g0241 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
a0001c0001t0004g0242 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
a0001c0001t0004g0243 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
a0001c0001t0004g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
a0001c0001t0004g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
a0001c0001t0004g0246 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
a0001c0001t0004g0251 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
a0001c0001t0004g0252 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
a0001c0001t0004g0253 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
a0001c0001t0004g0256 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
a0001c0001t0004g0257 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
a0001c0001t0004g0258 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
a0001c0001t0004g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
a0001c0001t0004g0260 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
a0001c0001t0004g0263 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
a0001c0001t0004g0265 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
a0001c0001t0004g0266 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
a0001c0001t0004g0268 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
a0001c0001t0004g0272 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
a0001c0001t0004g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
a0001c0001t0004g0274 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
a0001c0001t0004g0276 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
a0001c0001t0004g0282 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
a0001c0001t0004g0303 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
a0001c0001t0005g0277 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
a0001c0001t0005g0278 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
a0001c0001t0005g0279 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
a0001c0001t0005g0280 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
a0001c0001t0005g0281 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
a0001c0001t0005g0284 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
a0001c0001t0005g0285 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
a0001c0001t0005g0286 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
a0001c0001t0005g0287 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
a0001c0001t0006g0001 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
a0001c0001t0006g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
a0001c0001t0006g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
a0001c0001t0006g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
a0001c0001t0006g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
a0001c0001t0006g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
a0001c0001t0007g0255 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
a0001c0001t0008g0262 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
a0001c0001t0008g0267 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
a0001c0001t0008g0269 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
a0001c0001t0008g0270 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
a0001c0001t0008g0271 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
a0001c0001t0009g0289 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
a0001c0001t0009g0290 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
a0001c0001t0009g0291 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
a0001c0001t0009g0292 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
a0001c0001t0009g0293 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
a0001c0001t0011g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
a0001c0001t0011g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
a0001c0001t0011g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
a0001c0001t0013g0002 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
a0001c0001t0013g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
a0001c0001t0013g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
a0001c0001t0014g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
a0001c0001t0014g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
a0001c0001t0014g0296 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
a0001c0001t0015g0016 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
a0001c0001t0016g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
a0001c0001t0016g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
a0001c0001t0017g0028 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
a0001c0001t0018g0294 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
a0001c0001t0018g0304 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
a0001c0001t0020g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
a0001c0001t0021g0001 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
a0001c0001t0022g0033 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
a0001c0001t0023g0306 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
a0001c0001t0027g0236 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
a0001c0001t0028g0264 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
a0001c0001t0030g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
a0001c0001t0031g0037 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
a0001c0001t0032g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
a0001c0001t0034g0182 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
a0001c0001t0036g0288 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
a0001c0004t0024g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
a0001c0004t0025g0300 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
a0001c0004t0026g0305 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
a0001c0008t0008g0249 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
a0001c0009t0029g0295 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
a0002c0002t0001g0003 | 0/0 | 5 | 2 | 0 | 2 | 0 | 1 | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
a0002c0002t0001g0004 | 0/0 | 5 | 0 | 3 | 0 | 0 | 2 | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
a0002c0002t0001g0006 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
a0002c0002t0001g0007 | 0/0 | 4 | 0 | 1 | 0 | 1 | 2 | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
a0002c0002t0001g0008 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
a0002c0002t0001g0010 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
a0002c0002t0001g0011 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
a0002c0002t0001g0017 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
a0002c0002t0001g0018 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
a0002c0002t0001g0019 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
a0002c0002t0001g0020 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
a0002c0002t0001g0021 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
a0002c0002t0001g0022 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
a0002c0002t0001g0023 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
a0002c0002t0001g0024 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
a0002c0002t0001g0025 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
a0002c0002t0001g0083 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
a0002c0002t0001g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
a0002c0002t0001g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
a0002c0002t0001g0086 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
a0002c0002t0001g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
a0002c0002t0001g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
a0002c0002t0001g0092 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
a0002c0002t0001g0093 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
a0002c0002t0001g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
a0002c0002t0001g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
a0002c0002t0001g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
a0002c0002t0001g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
a0002c0002t0001g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
a0002c0002t0001g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
a0002c0002t0001g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
a0002c0002t0001g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
a0002c0002t0001g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
a0002c0002t0001g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
a0002c0002t0001g0106 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
a0002c0002t0001g0107 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
a0002c0002t0001g0108 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
a0002c0002t0001g0109 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
a0002c0002t0001g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
a0002c0002t0001g0112 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
a0002c0002t0001g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
a0002c0002t0001g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
a0002c0002t0001g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
a0002c0002t0001g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
a0002c0002t0001g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
a0002c0002t0001g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
a0002c0002t0001g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
a0002c0002t0001g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
a0002c0002t0001g0123 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
a0002c0002t0001g0124 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
a0002c0002t0001g0125 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
a0002c0002t0001g0126 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
a0002c0002t0001g0127 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
a0002c0002t0001g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
a0002c0002t0001g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
a0002c0002t0001g0132 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
a0002c0002t0001g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
a0002c0002t0001g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
a0002c0002t0001g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
a0002c0002t0001g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
a0002c0002t0001g0137 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
a0002c0002t0001g0138 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
a0002c0002t0001g0139 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
a0002c0002t0001g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
a0002c0002t0001g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
a0002c0002t0001g0143 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
a0002c0002t0001g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
a0002c0002t0001g0145 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
a0002c0002t0001g0146 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
a0002c0002t0001g0147 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
a0002c0002t0001g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
a0002c0002t0001g0149 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
a0002c0002t0001g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
a0002c0002t0001g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
a0002c0002t0001g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
a0002c0002t0001g0154 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
a0002c0002t0001g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
a0002c0002t0001g0156 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
a0002c0002t0001g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
a0002c0002t0001g0158 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
a0002c0002t0001g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
a0002c0002t0001g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
a0002c0002t0001g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
a0002c0002t0001g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
a0002c0002t0001g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
a0002c0002t0001g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
a0002c0002t0001g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
a0002c0002t0001g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
a0002c0002t0001g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
a0002c0002t0001g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
a0002c0002t0001g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
a0002c0002t0001g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
a0002c0002t0001g0171 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
a0002c0002t0001g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
a0002c0002t0001g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
a0002c0002t0001g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
a0002c0002t0001g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
a0002c0002t0001g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
a0002c0002t0001g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
a0002c0002t0010g0111 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
a0002c0002t0010g0122 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
a0002c0002t0010g0130 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
a0002c0002t0010g0131 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
a0002c0002t0012g0020 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
a0002c0002t0012g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
a0002c0002t0012g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
a0002c0002t0019g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
a0002c0002t0035g0010 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
a0002c0013t0001g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
a0003c0003t0007g0230 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
a0003c0003t0007g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
a0003c0003t0007g0247 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
a0003c0003t0007g0248 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
a0003c0003t0007g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
a0003c0003t0007g0254 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
a0003c0003t0007g0261 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
a0004c0005t0003g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
a0004c0005t0003g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
a0004c0005t0033g0009 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
a0005c0006t0011g0298 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
a0006c0015t0001g0140 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
a0007c0010t0002g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
a0008c0007t0002g0056 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
a0009c0014t0001g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
a0010c0012t0001g0008 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
a0011c0011t0004g0299 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0002 | c0002 | t0010 | g0130 | EUR | GBR | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
HG00099 | hp2 | a0001 | c0001 | t0002 | g0058 | EUR | GBR | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
HG00140 | hp1 | a0001 | c0001 | t0002 | g0034 | EUR | GBR | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
HG00140 | hp2 | a0002 | c0002 | t0001 | g0010 | EUR | GBR | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
HG00280 | hp1 | a0001 | c0001 | t0002 | g0052 | EUR | FIN | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
HG00280 | hp2 | a0001 | c0001 | t0003 | g0220 | EUR | FIN | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
HG00323 | hp1 | a0001 | c0001 | t0004 | g0014 | EUR | FIN | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
HG00323 | hp2 | a0002 | c0002 | t0001 | g0007 | EUR | FIN | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
HG00423 | hp1 | a0001 | c0001 | t0003 | g0206 | EAS | CHS | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
HG00423 | hp2 | a0001 | c0001 | t0002 | g0068 | EAS | CHS | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
HG00558 | hp1 | a0002 | c0002 | t0001 | g0021 | EAS | CHS | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
HG00558 | hp2 | a0001 | c0001 | t0002 | g0061 | EAS | CHS | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
HG00597 | hp1 | a0002 | c0002 | t0001 | g0153 | EAS | CHS | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
HG00597 | hp2 | a0001 | c0001 | t0004 | g0231 | EAS | CHS | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
HG00609 | hp1 | a0002 | c0002 | t0001 | g0168 | EAS | CHS | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
HG00609 | hp2 | a0001 | c0001 | t0003 | g0194 | EAS | CHS | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
HG00621 | hp1 | a0002 | c0002 | t0001 | g0160 | EAS | CHS | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
HG00621 | hp2 | a0001 | c0001 | t0006 | g0038 | EAS | CHS | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
HG00639 | hp1 | a0002 | c0002 | t0001 | g0018 | AMR | PUR | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
HG00639 | hp2 | a0002 | c0002 | t0001 | g0107 | AMR | PUR | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
HG00642 | hp1 | a0002 | c0002 | t0001 | g0109 | AMR | PUR | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
HG00642 | hp2 | a0001 | c0001 | t0004 | g0260 | AMR | PUR | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
HG00735 | hp1 | a0002 | c0002 | t0001 | g0004 | AMR | PUR | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
HG00735 | hp2 | a0001 | c0001 | t0004 | g0013 | AMR | PUR | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
HG00738 | hp1 | a0002 | c0002 | t0001 | g0106 | AMR | PUR | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
HG00738 | hp2 | a0001 | c0001 | t0004 | g0242 | AMR | PUR | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
HG00741 | hp1 | a0002 | c0002 | t0001 | g0108 | AMR | PUR | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
HG00741 | hp2 | a0001 | c0001 | t0002 | g0041 | AMR | PUR | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
HG01069 | hp1 | a0001 | c0001 | t0002 | g0053 | AMR | PUR | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
HG01069 | hp2 | a0001 | c0001 | t0003 | g0189 | AMR | PUR | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
HG01070 | hp1 | a0001 | c0001 | t0003 | g0222 | AMR | PUR | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
HG01070 | hp2 | a0002 | c0002 | t0001 | g0018 | AMR | PUR | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
HG01071 | hp1 | a0001 | c0001 | t0002 | g0001 | AMR | PUR | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
HG01071 | hp2 | a0001 | c0001 | t0003 | g0183 | AMR | PUR | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
HG01074 | hp1 | a0001 | c0001 | t0003 | g0199 | AMR | PUR | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
HG01074 | hp2 | a0002 | c0002 | t0001 | g0092 | AMR | PUR | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
HG01081 | hp1 | a0001 | c0001 | t0003 | g0026 | AMR | PUR | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
HG01081 | hp2 | a0002 | c0002 | t0001 | g0171 | AMR | PUR | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
HG01099 | hp1 | a0002 | c0002 | t0001 | g0004 | AMR | PUR | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
HG01099 | hp2 | a0001 | c0001 | t0004 | g0282 | AMR | PUR | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
HG01106 | hp1 | a0001 | c0001 | t0004 | g0002 | AMR | PUR | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
HG01106 | hp2 | a0001 | c0001 | t0003 | g0184 | AMR | PUR | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
HG01109 | hp1 | a0006 | c0015 | t0001 | g0140 | AMR | PUR | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
HG01109 | hp2 | a0008 | c0007 | t0002 | g0056 | AMR | PUR | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
HG01168 | hp1 | a0001 | c0001 | t0003 | g0221 | AMR | PUR | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
HG01168 | hp2 | a0002 | c0002 | t0001 | g0127 | AMR | PUR | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
HG01175 | hp1 | a0003 | c0003 | t0007 | g0230 | AMR | PUR | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
HG01175 | hp2 | a0001 | c0001 | t0002 | g0032 | AMR | PUR | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
HG01243 | hp1 | a0001 | c0004 | t0026 | g0305 | AMR | PUR | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
HG01243 | hp2 | a0001 | c0001 | t0028 | g0264 | AMR | PUR | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
HG01255 | hp1 | a0001 | c0001 | t0002 | g0001 | AMR | CLM | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
HG01255 | hp2 | a0001 | c0001 | t0003 | g0009 | AMR | CLM | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
HG01257 | hp1 | a0001 | c0001 | t0004 | g0265 | AMR | CLM | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
HG01257 | hp2 | a0001 | c0001 | t0003 | g0188 | AMR | CLM | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
HG01261 | hp1 | a0002 | c0002 | t0010 | g0122 | AMR | CLM | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
HG01261 | hp2 | a0001 | c0001 | t0002 | g0001 | AMR | CLM | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
HG01346 | hp1 | a0002 | c0002 | t0001 | g0024 | AMR | CLM | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
HG01346 | hp2 | a0002 | c0002 | t0001 | g0093 | AMR | CLM | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
HG01361 | hp1 | a0002 | c0002 | t0001 | g0139 | AMR | CLM | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
HG01361 | hp2 | a0001 | c0001 | t0003 | g0200 | AMR | CLM | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
HG01433 | hp1 | a0002 | c0002 | t0001 | g0156 | AMR | CLM | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
HG01433 | hp2 | a0001 | c0001 | t0027 | g0236 | AMR | CLM | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
HG01496 | hp1 | a0002 | c0002 | t0001 | g0011 | AMR | CLM | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
HG01496 | hp2 | a0002 | c0002 | t0001 | g0007 | AMR | CLM | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
HG01515 | hp1 | a0001 | c0001 | t0003 | g0026 | EUR | IBS | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
HG01515 | hp2 | a0002 | c0002 | t0001 | g0132 | EUR | IBS | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
HG01516 | hp1 | a0001 | c0001 | t0004 | g0274 | EUR | IBS | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
HG01516 | hp2 | a0001 | c0001 | t0003 | g0203 | EUR | IBS | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
HG01517 | hp1 | a0001 | c0001 | t0004 | g0243 | EUR | IBS | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
HG01517 | hp2 | a0002 | c0002 | t0001 | g0010 | EUR | IBS | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
HG01884 | hp1 | a0001 | c0001 | t0009 | g0293 | AFR | ACB | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
HG01884 | hp2 | a0001 | c0001 | t0008 | g0267 | AFR | ACB | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
HG01891 | hp1 | a0001 | c0001 | t0005 | g0278 | AFR | ACB | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
HG01891 | hp2 | a0001 | c0001 | t0011 | g0227 | AFR | ACB | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
HG01943 | hp1 | a0002 | c0002 | t0001 | g0011 | AMR | PEL | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
HG01943 | hp2 | a0002 | c0002 | t0010 | g0131 | AMR | PEL | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
HG01978 | hp1 | a0001 | c0001 | t0002 | g0042 | AMR | PEL | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
HG01978 | hp2 | a0002 | c0002 | t0001 | g0154 | AMR | PEL | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
HG01981 | hp1 | a0002 | c0002 | t0001 | g0112 | AMR | PEL | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
HG01981 | hp2 | a0001 | c0001 | t0004 | g0002 | AMR | PEL | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
HG01993 | hp1 | a0002 | c0002 | t0001 | g0004 | AMR | PEL | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
HG01993 | hp2 | a0001 | c0001 | t0004 | g0014 | AMR | PEL | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
HG02004 | hp1 | a0001 | c0001 | t0004 | g0002 | AMR | PEL | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
HG02004 | hp2 | a0002 | c0002 | t0001 | g0011 | AMR | PEL | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
HG02027 | hp1 | a0002 | c0002 | t0001 | g0087 | EAS | KHV | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
HG02027 | hp2 | a0001 | c0001 | t0003 | g0211 | EAS | KHV | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
HG02040 | hp1 | a0001 | c0001 | t0021 | g0001 | EAS | KHV | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
HG02040 | hp2 | a0010 | c0012 | t0001 | g0008 | EAS | KHV | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
HG02055 | hp1 | a0001 | c0001 | t0011 | g0228 | AFR | ACB | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
HG02055 | hp2 | a0002 | c0002 | t0001 | g0096 | AFR | ACB | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
HG02056 | hp1 | a0002 | c0002 | t0001 | g0085 | EAS | KHV | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
HG02056 | hp2 | a0001 | c0001 | t0003 | g0216 | EAS | KHV | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
HG02074 | hp1 | a0001 | c0001 | t0002 | g0050 | EAS | KHV | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
HG02074 | hp2 | a0002 | c0002 | t0001 | g0115 | EAS | KHV | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
HG02129 | hp1 | a0001 | c0001 | t0003 | g0027 | EAS | KHV | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
HG02129 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | KHV | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
HG02132 | hp1 | a0001 | c0001 | t0002 | g0072 | EAS | KHV | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
HG02132 | hp2 | a0002 | c0002 | t0001 | g0166 | EAS | KHV | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
HG02135 | hp1 | a0002 | c0002 | t0001 | g0102 | EAS | KHV | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
HG02135 | hp2 | a0001 | c0001 | t0003 | g0217 | EAS | KHV | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
HG02145 | hp1 | a0002 | c0002 | t0001 | g0095 | AFR | ACB | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
HG02145 | hp2 | a0001 | c0001 | t0005 | g0287 | AFR | ACB | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
HG02155 | hp1 | a0001 | c0001 | t0006 | g0001 | EAS | CDX | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
HG02155 | hp2 | a0002 | c0002 | t0001 | g0006 | EAS | CDX | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
HG02257 | hp1 | a0001 | c0001 | t0004 | g0233 | AFR | ACB | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
HG02257 | hp2 | a0001 | c0001 | t0007 | g0255 | AFR | ACB | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
HG02258 | hp1 | a0001 | c0001 | t0004 | g0029 | AFR | ACB | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
HG02258 | hp2 | a0001 | c0001 | t0009 | g0291 | AFR | ACB | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
HG02273 | hp1 | a0002 | c0002 | t0001 | g0024 | AMR | PEL | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
HG02273 | hp2 | a0001 | c0001 | t0004 | g0002 | AMR | PEL | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
HG02280 | hp1 | a0001 | c0001 | t0004 | g0263 | AFR | ACB | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
HG02280 | hp2 | a0001 | c0001 | t0005 | g0281 | AFR | ACB | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
HG02300 | hp1 | a0002 | c0002 | t0001 | g0158 | AMR | PEL | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
HG02300 | hp2 | a0001 | c0001 | t0034 | g0182 | AMR | PEL | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
HG02451 | hp1 | a0001 | c0001 | t0003 | g0195 | AFR | ACB | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
HG02451 | hp2 | a0001 | c0001 | t0004 | g0268 | AFR | ACB | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
HG02523 | hp1 | a0002 | c0002 | t0001 | g0103 | EAS | KHV | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
HG02523 | hp2 | a0002 | c0002 | t0001 | g0020 | EAS | KHV | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
HG02572 | hp1 | a0001 | c0001 | t0003 | g0198 | AFR | GWD | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
HG02572 | hp2 | a0003 | c0003 | t0007 | g0235 | AFR | GWD | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
HG02602 | hp1 | a0002 | c0002 | t0001 | g0143 | SAS | PJL | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
HG02602 | hp2 | a0011 | c0011 | t0004 | g0299 | SAS | PJL | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
HG02622 | hp1 | a0005 | c0006 | t0011 | g0298 | AFR | GWD | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
HG02622 | hp2 | a0001 | c0001 | t0036 | g0288 | AFR | GWD | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
HG02630 | hp1 | a0001 | c0001 | t0004 | g0257 | AFR | GWD | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
HG02630 | hp2 | a0003 | c0003 | t0007 | g0261 | AFR | GWD | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
HG02647 | hp1 | a0001 | c0001 | t0008 | g0262 | AFR | GWD | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
HG02647 | hp2 | a0001 | c0004 | t0025 | g0300 | AFR | GWD | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
HG02683 | hp1 | a0002 | c0002 | t0001 | g0007 | SAS | PJL | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
HG02683 | hp2 | a0001 | c0001 | t0004 | g0266 | SAS | PJL | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
HG02698 | hp1 | a0001 | c0001 | t0004 | g0258 | SAS | PJL | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
HG02698 | hp2 | a0001 | c0001 | t0002 | g0066 | SAS | PJL | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
HG02717 | hp1 | a0002 | c0002 | t0001 | g0118 | AFR | GWD | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
HG02717 | hp2 | a0002 | c0002 | t0001 | g0104 | AFR | GWD | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
HG02723 | hp1 | a0001 | c0001 | t0018 | g0294 | AFR | GWD | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
HG02723 | hp2 | a0001 | c0001 | t0003 | g0009 | AFR | GWD | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
HG02735 | hp1 | a0002 | c0002 | t0001 | g0123 | SAS | PJL | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
HG02735 | hp2 | a0001 | c0001 | t0004 | g0238 | SAS | PJL | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
HG02738 | hp1 | a0002 | c0002 | t0001 | g0125 | SAS | PJL | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
HG02738 | hp2 | a0001 | c0001 | t0002 | g0070 | SAS | PJL | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
HG02809 | hp1 | a0001 | c0001 | t0005 | g0285 | AFR | GWD | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
HG02809 | hp2 | a0003 | c0003 | t0007 | g0250 | AFR | GWD | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
HG02818 | hp1 | a0001 | c0001 | t0009 | g0292 | AFR | GWD | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
HG02818 | hp2 | a0003 | c0003 | t0007 | g0248 | AFR | GWD | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
HG02886 | hp1 | a0001 | c0001 | t0008 | g0271 | AFR | GWD | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
HG02886 | hp2 | a0001 | c0001 | t0005 | g0277 | AFR | GWD | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
HG02895 | hp1 | a0001 | c0001 | t0017 | g0028 | AFR | GWD | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
HG02895 | hp2 | a0001 | c0001 | t0004 | g0253 | AFR | GWD | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
HG02896 | hp1 | a0002 | c0002 | t0001 | g0129 | AFR | GWD | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
HG02896 | hp2 | a0001 | c0001 | t0003 | g0223 | AFR | GWD | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
HG02897 | hp1 | a0001 | c0001 | t0003 | g0192 | AFR | GWD | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
HG02897 | hp2 | a0001 | c0001 | t0004 | g0244 | AFR | GWD | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
HG02922 | hp1 | a0002 | c0002 | t0001 | g0105 | AFR | ESN | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
HG02922 | hp2 | a0001 | c0001 | t0008 | g0270 | AFR | ESN | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
HG02965 | hp1 | a0001 | c0001 | t0002 | g0081 | AFR | ESN | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
HG02965 | hp2 | a0001 | c0001 | t0004 | g0276 | AFR | ESN | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
HG02970 | hp1 | a0001 | c0001 | t0004 | g0303 | AFR | ESN | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
HG02970 | hp2 | a0009 | c0014 | t0001 | g0094 | AFR | ESN | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
HG03017 | hp1 | a0002 | c0002 | t0001 | g0086 | SAS | PJL | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
HG03017 | hp2 | a0002 | c0002 | t0001 | g0126 | SAS | PJL | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
HG03041 | hp1 | a0001 | c0001 | t0004 | g0225 | AFR | GWD | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
HG03041 | hp2 | a0002 | c0002 | t0001 | g0017 | AFR | GWD | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
HG03098 | hp1 | a0001 | c0001 | t0003 | g0208 | AFR | MSL | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
HG03098 | hp2 | a0001 | c0001 | t0014 | g0296 | AFR | MSL | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
HG03130 | hp1 | a0001 | c0001 | t0017 | g0028 | AFR | ESN | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
HG03130 | hp2 | a0001 | c0001 | t0004 | g0029 | AFR | ESN | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
HG03139 | hp1 | a0002 | c0002 | t0001 | g0099 | AFR | ESN | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
HG03139 | hp2 | a0001 | c0001 | t0018 | g0304 | AFR | ESN | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
HG03195 | hp1 | a0001 | c0001 | t0004 | g0256 | AFR | ESN | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
HG03195 | hp2 | a0001 | c0009 | t0029 | g0295 | AFR | ESN | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
HG03209 | hp1 | a0001 | c0001 | t0009 | g0289 | AFR | MSL | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
HG03209 | hp2 | a0001 | c0001 | t0008 | g0269 | AFR | MSL | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
HG03225 | hp1 | a0001 | c0001 | t0003 | g0191 | AFR | MSL | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
HG03225 | hp2 | a0001 | c0001 | t0023 | g0306 | AFR | MSL | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
HG03239 | hp1 | a0002 | c0002 | t0001 | g0004 | SAS | PJL | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
HG03239 | hp2 | a0002 | c0002 | t0001 | g0019 | SAS | PJL | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
HG03453 | hp1 | a0001 | c0001 | t0009 | g0290 | AFR | MSL | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
HG03453 | hp2 | a0001 | c0001 | t0002 | g0079 | AFR | MSL | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
HG03486 | hp1 | a0001 | c0001 | t0030 | g0224 | AFR | MSL | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
HG03486 | hp2 | a0001 | c0001 | t0014 | g0178 | AFR | MSL | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
HG03490 | hp1 | a0001 | c0001 | t0015 | g0016 | SAS | PJL | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
HG03490 | hp2 | a0002 | c0002 | t0001 | g0004 | SAS | PJL | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
HG03491 | hp1 | a0001 | c0001 | t0003 | g0196 | SAS | PJL | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
HG03491 | hp2 | a0002 | c0002 | t0001 | g0145 | SAS | PJL | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
HG03492 | hp1 | a0002 | c0002 | t0001 | g0146 | SAS | PJL | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
HG03492 | hp2 | a0001 | c0001 | t0015 | g0016 | SAS | PJL | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
HG03516 | hp1 | a0007 | c0010 | t0002 | g0090 | AFR | ESN | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
HG03516 | hp2 | a0001 | c0001 | t0005 | g0279 | AFR | ESN | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
HG03579 | hp1 | a0001 | c0001 | t0004 | g0251 | AFR | MSL | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
HG03579 | hp2 | a0001 | c0001 | t0004 | g0226 | AFR | MSL | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
HG03654 | hp1 | a0002 | c0002 | t0001 | g0007 | SAS | PJL | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
HG03654 | hp2 | a0001 | c0001 | t0004 | g0272 | SAS | PJL | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
HG03688 | hp1 | a0001 | c0001 | t0004 | g0030 | SAS | STU | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
HG03688 | hp2 | a0001 | c0001 | t0002 | g0035 | SAS | STU | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
HG03704 | hp1 | a0002 | c0002 | t0001 | g0019 | SAS | PJL | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
HG03704 | hp2 | a0001 | c0001 | t0002 | g0049 | SAS | PJL | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
HG03831 | hp1 | a0001 | c0001 | t0031 | g0037 | SAS | BEB | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
HG03831 | hp2 | a0001 | c0001 | t0003 | g0215 | SAS | BEB | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
HG03942 | hp1 | a0001 | c0001 | t0003 | g0202 | SAS | BEB | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
HG03942 | hp2 | a0001 | c0001 | t0022 | g0033 | SAS | BEB | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
HG04115 | hp1 | a0002 | c0002 | t0001 | g0083 | SAS | STU | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
HG04115 | hp2 | a0002 | c0002 | t0001 | g0124 | SAS | STU | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
HG04199 | hp1 | a0001 | c0001 | t0002 | g0089 | SAS | STU | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
HG04199 | hp2 | a0001 | c0001 | t0004 | g0013 | SAS | STU | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
HG04204 | hp1 | a0002 | c0002 | t0001 | g0003 | SAS | STU | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
HG04204 | hp2 | a0001 | c0001 | t0002 | g0067 | SAS | STU | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
NA18522 | hp1 | a0002 | c0002 | t0001 | g0003 | AFR | YRI | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
NA18522 | hp2 | a0001 | c0001 | t0014 | g0179 | AFR | YRI | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
NA18612 | hp1 | a0002 | c0002 | t0001 | g0175 | EAS | CHB | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
NA18612 | hp2 | a0001 | c0001 | t0006 | g0001 | EAS | CHB | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
NA18747 | hp1 | a0002 | c0002 | t0001 | g0119 | EAS | CHB | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
NA18747 | hp2 | a0001 | c0001 | t0002 | g0077 | EAS | CHB | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
NA18906 | hp1 | a0001 | c0001 | t0016 | g0048 | AFR | YRI | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
NA18906 | hp2 | a0001 | c0001 | t0005 | g0286 | AFR | YRI | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
NA18939 | hp1 | a0002 | c0002 | t0001 | g0165 | EAS | JPT | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
NA18939 | hp2 | a0001 | c0001 | t0002 | g0076 | EAS | JPT | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
NA18943 | hp1 | a0002 | c0002 | t0001 | g0121 | EAS | JPT | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
NA18943 | hp2 | a0001 | c0001 | t0002 | g0015 | EAS | JPT | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
NA18944 | hp1 | a0001 | c0001 | t0004 | g0259 | EAS | JPT | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
NA18944 | hp2 | a0002 | c0002 | t0001 | g0008 | EAS | JPT | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
NA18946 | hp1 | a0001 | c0001 | t0002 | g0054 | EAS | JPT | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
NA18946 | hp2 | a0002 | c0002 | t0001 | g0142 | EAS | JPT | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
NA18947 | hp1 | a0002 | c0013 | t0001 | g0101 | EAS | JPT | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
NA18947 | hp2 | a0001 | c0004 | t0024 | g0283 | EAS | JPT | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
NA18948 | hp1 | a0001 | c0001 | t0002 | g0039 | EAS | JPT | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
NA18948 | hp2 | a0002 | c0002 | t0001 | g0162 | EAS | JPT | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
NA18949 | hp1 | a0001 | c0001 | t0020 | g0064 | EAS | JPT | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
NA18949 | hp2 | a0002 | c0002 | t0001 | g0170 | EAS | JPT | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
NA18951 | hp1 | a0002 | c0002 | t0001 | g0177 | EAS | JPT | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
NA18951 | hp2 | a0001 | c0001 | t0003 | g0009 | EAS | JPT | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
NA18952 | hp1 | a0002 | c0002 | t0001 | g0025 | EAS | JPT | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
NA18952 | hp2 | a0001 | c0001 | t0002 | g0055 | EAS | JPT | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
NA18953 | hp1 | a0001 | c0001 | t0013 | g0275 | EAS | JPT | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
NA18953 | hp2 | a0002 | c0002 | t0001 | g0023 | EAS | JPT | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
NA18954 | hp1 | a0001 | c0001 | t0003 | g0213 | EAS | JPT | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
NA18954 | hp2 | a0001 | c0001 | t0004 | g0237 | EAS | JPT | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
NA18956 | hp1 | a0001 | c0001 | t0003 | g0212 | EAS | JPT | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
NA18956 | hp2 | a0002 | c0002 | t0001 | g0173 | EAS | JPT | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
NA18957 | hp1 | a0002 | c0002 | t0001 | g0163 | EAS | JPT | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
NA18957 | hp2 | a0002 | c0002 | t0001 | g0128 | EAS | JPT | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
NA18962 | hp1 | a0002 | c0002 | t0001 | g0151 | EAS | JPT | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
NA18962 | hp2 | a0001 | c0001 | t0002 | g0046 | EAS | JPT | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
NA18964 | hp1 | a0002 | c0002 | t0001 | g0164 | EAS | JPT | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
NA18964 | hp2 | a0001 | c0001 | t0004 | g0239 | EAS | JPT | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
NA18965 | hp1 | a0002 | c0002 | t0001 | g0172 | EAS | JPT | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
NA18965 | hp2 | a0001 | c0001 | t0003 | g0218 | EAS | JPT | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
NA18966 | hp1 | a0002 | c0002 | t0001 | g0141 | EAS | JPT | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
NA18966 | hp2 | a0004 | c0005 | t0003 | g0185 | EAS | JPT | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
NA18967 | hp1 | a0001 | c0001 | t0003 | g0205 | EAS | JPT | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
NA18967 | hp2 | a0001 | c0001 | t0002 | g0047 | EAS | JPT | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
NA18968 | hp1 | a0002 | c0002 | t0001 | g0176 | EAS | JPT | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
NA18968 | hp2 | a0001 | c0001 | t0002 | g0088 | EAS | JPT | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
NA18969 | hp1 | a0002 | c0002 | t0001 | g0159 | EAS | JPT | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
NA18969 | hp2 | a0001 | c0001 | t0004 | g0002 | EAS | JPT | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
NA18971 | hp1 | a0001 | c0001 | t0032 | g0209 | EAS | JPT | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
NA18971 | hp2 | a0002 | c0002 | t0001 | g0152 | EAS | JPT | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
NA18972 | hp1 | a0002 | c0002 | t0001 | g0098 | EAS | JPT | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
NA18972 | hp2 | a0001 | c0001 | t0003 | g0201 | EAS | JPT | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
NA18974 | hp1 | a0001 | c0001 | t0003 | g0214 | EAS | JPT | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
NA18974 | hp2 | a0001 | c0001 | t0002 | g0069 | EAS | JPT | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
NA18977 | hp1 | a0001 | c0001 | t0003 | g0197 | EAS | JPT | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
NA18977 | hp2 | a0001 | c0001 | t0002 | g0060 | EAS | JPT | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
NA18982 | hp1 | a0001 | c0001 | t0002 | g0051 | EAS | JPT | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
NA18982 | hp2 | a0001 | c0001 | t0003 | g0193 | EAS | JPT | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
NA18983 | hp1 | a0001 | c0001 | t0002 | g0005 | EAS | JPT | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
NA18983 | hp2 | a0002 | c0002 | t0001 | g0003 | EAS | JPT | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
NA18984 | hp1 | a0001 | c0001 | t0002 | g0065 | EAS | JPT | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
NA18984 | hp2 | a0002 | c0002 | t0001 | g0008 | EAS | JPT | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
NA18985 | hp1 | a0002 | c0002 | t0001 | g0110 | EAS | JPT | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
NA18985 | hp2 | a0002 | c0002 | t0012 | g0082 | EAS | JPT | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
NA18987 | hp1 | a0001 | c0001 | t0006 | g0001 | EAS | JPT | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
NA18987 | hp2 | a0002 | c0002 | t0001 | g0116 | EAS | JPT | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
NA18988 | hp1 | a0002 | c0002 | t0001 | g0148 | EAS | JPT | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
NA18988 | hp2 | a0001 | c0001 | t0006 | g0063 | EAS | JPT | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
NA18989 | hp1 | a0002 | c0002 | t0001 | g0134 | EAS | JPT | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
NA18989 | hp2 | a0004 | c0005 | t0033 | g0009 | EAS | JPT | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
NA18990 | hp1 | a0002 | c0002 | t0001 | g0113 | EAS | JPT | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
NA18990 | hp2 | a0001 | c0001 | t0004 | g0180 | EAS | JPT | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
NA18991 | hp1 | a0002 | c0002 | t0001 | g0021 | EAS | JPT | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
NA18991 | hp2 | a0001 | c0001 | t0004 | g0232 | EAS | JPT | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
NA18992 | hp1 | a0001 | c0001 | t0004 | g0273 | EAS | JPT | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
NA18992 | hp2 | a0001 | c0001 | t0002 | g0040 | EAS | JPT | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
NA18994 | hp1 | a0001 | c0001 | t0002 | g0044 | EAS | JPT | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
NA18994 | hp2 | a0002 | c0002 | t0001 | g0174 | EAS | JPT | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
NA18999 | hp1 | a0001 | c0001 | t0002 | g0005 | EAS | JPT | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
NA18999 | hp2 | a0001 | c0001 | t0003 | g0204 | EAS | JPT | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
NA19000 | hp1 | a0002 | c0002 | t0001 | g0120 | EAS | JPT | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
NA19000 | hp2 | a0001 | c0001 | t0002 | g0074 | EAS | JPT | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
NA19003 | hp1 | a0002 | c0002 | t0001 | g0157 | EAS | JPT | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
NA19003 | hp2 | a0001 | c0001 | t0003 | g0297 | EAS | JPT | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
NA19004 | hp1 | a0002 | c0002 | t0001 | g0006 | EAS | JPT | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
NA19004 | hp2 | a0001 | c0001 | t0013 | g0030 | EAS | JPT | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
NA19007 | hp1 | a0001 | c0001 | t0004 | g0240 | EAS | JPT | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
NA19007 | hp2 | a0002 | c0002 | t0001 | g0084 | EAS | JPT | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
NA19009 | hp1 | a0002 | c0002 | t0001 | g0022 | EAS | JPT | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
NA19009 | hp2 | a0001 | c0001 | t0002 | g0005 | EAS | JPT | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
NA19011 | hp1 | a0002 | c0002 | t0001 | g0023 | EAS | JPT | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
NA19011 | hp2 | a0001 | c0001 | t0002 | g0043 | EAS | JPT | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
NA19043 | hp1 | a0001 | c0001 | t0004 | g0252 | AFR | LWK | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
NA19043 | hp2 | a0003 | c0003 | t0007 | g0247 | AFR | LWK | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
NA19054 | hp1 | a0001 | c0001 | t0004 | g0002 | EAS | JPT | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
NA19054 | hp2 | a0002 | c0002 | t0001 | g0091 | EAS | JPT | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
NA19055 | hp1 | a0001 | c0001 | t0003 | g0190 | EAS | JPT | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
NA19055 | hp2 | a0002 | c0002 | t0001 | g0169 | EAS | JPT | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
NA19056 | hp1 | a0001 | c0001 | t0003 | g0012 | EAS | JPT | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
NA19056 | hp2 | a0002 | c0002 | t0001 | g0025 | EAS | JPT | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
NA19058 | hp1 | a0002 | c0002 | t0001 | g0022 | EAS | JPT | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
NA19058 | hp2 | a0001 | c0001 | t0003 | g0187 | EAS | JPT | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
NA19059 | hp1 | a0001 | c0001 | t0006 | g0073 | EAS | JPT | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
NA19059 | hp2 | a0001 | c0001 | t0003 | g0301 | EAS | JPT | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
NA19060 | hp1 | a0002 | c0002 | t0001 | g0133 | EAS | JPT | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
NA19060 | hp2 | a0001 | c0001 | t0006 | g0057 | EAS | JPT | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
NA19062 | hp1 | a0001 | c0001 | t0013 | g0002 | EAS | JPT | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
NA19062 | hp2 | a0002 | c0002 | t0001 | g0155 | EAS | JPT | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
NA19063 | hp1 | a0001 | c0001 | t0004 | g0014 | EAS | JPT | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
NA19063 | hp2 | a0001 | c0001 | t0002 | g0062 | EAS | JPT | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
NA19064 | hp1 | a0001 | c0001 | t0004 | g0013 | EAS | JPT | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
NA19064 | hp2 | a0001 | c0001 | t0006 | g0001 | EAS | JPT | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
NA19066 | hp1 | a0002 | c0002 | t0001 | g0136 | EAS | JPT | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
NA19066 | hp2 | a0001 | c0001 | t0002 | g0071 | EAS | JPT | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
NA19070 | hp1 | a0001 | c0001 | t0003 | g0027 | EAS | JPT | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
NA19070 | hp2 | a0001 | c0001 | t0006 | g0059 | EAS | JPT | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
NA19072 | hp1 | a0001 | c0001 | t0003 | g0012 | EAS | JPT | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
NA19072 | hp2 | a0001 | c0001 | t0002 | g0045 | EAS | JPT | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
NA19075 | hp1 | a0002 | c0002 | t0001 | g0003 | EAS | JPT | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
NA19075 | hp2 | a0002 | c0002 | t0012 | g0020 | EAS | JPT | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
NA19077 | hp1 | a0002 | c0002 | t0001 | g0117 | EAS | JPT | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
NA19077 | hp2 | a0001 | c0001 | t0003 | g0302 | EAS | JPT | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
NA19079 | hp1 | a0001 | c0001 | t0002 | g0075 | EAS | JPT | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
NA19079 | hp2 | a0002 | c0002 | t0012 | g0150 | EAS | JPT | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
NA19080 | hp1 | a0002 | c0002 | t0001 | g0006 | EAS | JPT | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
NA19080 | hp2 | a0001 | c0001 | t0003 | g0219 | EAS | JPT | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
NA19081 | hp1 | a0002 | c0002 | t0001 | g0161 | EAS | JPT | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
NA19081 | hp2 | a0001 | c0001 | t0002 | g0015 | EAS | JPT | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
NA19084 | hp1 | a0002 | c0002 | t0001 | g0008 | EAS | JPT | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
NA19084 | hp2 | a0002 | c0002 | t0019 | g0114 | EAS | JPT | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
NA19087 | hp1 | a0001 | c0001 | t0002 | g0078 | EAS | JPT | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
NA19087 | hp2 | a0002 | c0002 | t0001 | g0100 | EAS | JPT | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
NA19088 | hp1 | a0001 | c0001 | t0002 | g0005 | EAS | JPT | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
NA19088 | hp2 | a0004 | c0005 | t0003 | g0181 | EAS | JPT | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
NA19089 | hp1 | a0001 | c0001 | t0003 | g0210 | EAS | JPT | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
NA19089 | hp2 | a0002 | c0002 | t0001 | g0167 | EAS | JPT | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
NA19090 | hp1 | a0001 | c0001 | t0003 | g0207 | EAS | JPT | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
NA19090 | hp2 | a0002 | c0002 | t0001 | g0135 | EAS | JPT | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
NA19240 | hp1 | a0001 | c0001 | t0004 | g0246 | AFR | YRI | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
NA19240 | hp2 | a0001 | c0001 | t0005 | g0280 | AFR | YRI | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
NA20129 | hp1 | a0001 | c0008 | t0008 | g0249 | AFR | ASW | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
NA20129 | hp2 | a0002 | c0002 | t0001 | g0017 | AFR | ASW | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
NA20752 | hp1 | a0001 | c0001 | t0004 | g0241 | EUR | TSI | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
NA20752 | hp2 | a0002 | c0002 | t0001 | g0137 | EUR | TSI | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
NA20805 | hp1 | a0002 | c0002 | t0001 | g0149 | EUR | TSI | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
NA20805 | hp2 | a0001 | c0001 | t0002 | g0001 | EUR | TSI | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
NA20905 | hp1 | a0002 | c0002 | t0035 | g0010 | SAS | GIH | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
NA20905 | hp2 | a0001 | c0001 | t0004 | g0002 | SAS | GIH | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
HG01123 | hp1 | a0002 | c0002 | t0001 | g0138 | AMR | CLM | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
HG01123 | hp2 | a0001 | c0001 | t0002 | g0031 | AMR | CLM | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
HG02109 | hp1 | a0001 | c0001 | t0005 | g0284 | AFR | ACB | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
HG02109 | hp2 | a0002 | c0002 | t0001 | g0097 | AFR | ACB | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
HG02486 | hp1 | a0003 | c0003 | t0007 | g0254 | AFR | ACB | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
HG02486 | hp2 | a0001 | c0001 | t0002 | g0080 | AFR | ACB | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
HG03471 | hp1 | a0001 | c0001 | t0003 | g0186 | AFR | MSL | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
HG03471 | hp2 | a0001 | c0001 | t0011 | g0229 | AFR | MSL | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
HG06807 | hp1 | a0001 | c0001 | t0004 | g0245 | AFR | USA | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
HG06807 | hp2 | a0001 | c0001 | t0002 | g0001 | AFR | USA | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
NA18955 | hp1 | a0001 | c0001 | t0003 | g0012 | EAS | JPT | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
NA18955 | hp2 | a0002 | c0002 | t0001 | g0006 | EAS | JPT | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
NA20300 | hp1 | a0002 | c0002 | t0001 | g0003 | AFR | USA | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
NA20300 | hp2 | a0001 | c0001 | t0016 | g0036 | AFR | USA | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
NA21309 | hp1 | a0002 | c0002 | t0001 | g0144 | AFR | LWK | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
NA21309 | hp2 | a0001 | c0001 | t0004 | g0234 | AFR | LWK | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
homoSapiens_chm13v2 | hp1 | a0002 | c0002 | t0001 | g0147 | REF | REF | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
homoSapiens_grch38 | hp1 | a0002 | c0002 | t0010 | g0111 | REF | REF | GFM1_chr3_158639527_158700581 | GFM1 | chr3 | 158639527 | 158700581 |
chr:pos | ref | alt | # # of ahapid:amino-acid(protein) level |
ahapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr3:158644711
|
A | G | 1 | a0011 | 1 | HG02602.hp2 | missense_variant | MODERATE | c.77A>G | p.Lys26Arg | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 1/18 | 185/6478 | 77/2256 | 26/751 | chr3 | 158644711 | ||
chr3:158645635
|
TGGAAGGC others(4): Show |
T | 1 | a0005 | 1 | HG02622.hp1 | frameshift_variant | HIGH | c.89_99delGGAAGGCCTG others(1): Show |
p.Trp30fs | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 2/18 | 197/6478 | 89/2256 | 30/751 | chr3 | 158645635 | ||
chr3:158645674
|
A | G | 1 | a0006 | 1 | HG01109.hp1 | missense_variant | MODERATE | c.127A>G | p.Asn43Asp | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 2/18 | 235/6478 | 127/2256 | 43/751 | chr3 | 158645674 | ||
chr3:158646851
|
A | G | 1 | a0003 | 7 | HG01175.hp1 HG02486.hp1 HG02572.hp2 others(4): Show |
missense_variant | MODERATE | c.476A>G | p.Asn159Ser | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 4/18 | 584/6478 | 476/2256 | 159/751 | chr3 | 158646851 | ||
chr3:158646943
|
A | C | 1 | a0007 | 1 | HG03516.hp1 | missense_variant | MODERATE | c.568A>C | p.Met190Leu | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 4/18 | 676/6478 | 568/2256 | 190/751 | chr3 | 158646943 | ||
chr3:158649064
|
C | T | 1 | a0004 | 3 | NA18966.hp2 NA18989.hp2 NA19088.hp2 |
missense_variant | MODERATE | c.596C>T | p.Ala199Val | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 5/18 | 704/6478 | 596/2256 | 199/751 | chr3 | 158649064 | ||
chr3:158649090
|
G | A | 1 | a0010 | 1 | HG02040.hp2 | missense_variant | MODERATE | c.622G>A | p.Glu208Lys | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 5/18 | 730/6478 | 622/2256 | 208/751 | chr3 | 158649090 | ||
chr3:158649111
|
G | A | 7 | a0001a0003a0004others(4): Show | 233 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(230): Show |
missense_variant | MODERATE | c.643G>A | p.Val215Ile | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 5/18 | 751/6478 | 643/2256 | 215/751 | chr3 | 158649111 | ||
chr3:158662647
|
A | G | 1 | a0009 | 1 | HG02970.hp2 | missense_variant | MODERATE | c.1343A>G | p.Asp448Gly | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 11/18 | 1451/6478 | 1343/2256 | 448/751 | chr3 | 158662647 | ||
chr3:158690264
|
C | T | 1 | a0008 | 1 | HG01109.hp2 | missense_variant | MODERATE | c.2011C>T | p.Arg671Cys | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 16/18 | 2119/6478 | 2011/2256 | 671/751 | chr3 | 158690264 |
chr:pos | ref | alt | # # of chapid |
chapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr3:158644652
|
T | C | 10 | a0001c0001a0001c0004a0001c0008others(7): Show | 233 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(230): Show |
synonymous_variant | LOW | c.18T>C | p.Ala6Ala | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 1/18 | 126/6478 | 18/2256 | 6/751 | chr3 | 158644652 | ||
chr3:158652111
|
T | C | 1 | a0006c0015 | 1 | HG01109.hp1 | synonymous_variant | LOW | c.705T>C | p.Tyr235Tyr | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 6/18 | 813/6478 | 705/2256 | 235/751 | chr3 | 158652111 | ||
chr3:158659047
|
C | T | 1 | a0001c0004 | 3 | HG01243.hp1 HG02647.hp2 NA18947.hp2 |
synonymous_variant | LOW | c.1209C>T | p.Ala403Ala | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 9/18 | 1317/6478 | 1209/2256 | 403/751 | chr3 | 158659047 | ||
chr3:158666378
|
C | T | 1 | a0001c0009 | 1 | HG03195.hp2 | synonymous_variant | LOW | c.1593C>T | p.Ala531Ala | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 13/18 | 1701/6478 | 1593/2256 | 531/751 | chr3 | 158666378 | ||
chr3:158682103
|
A | G | 1 | a0002c0013 | 1 | NA18947.hp1 | synonymous_variant | LOW | c.1710A>G | p.Ser570Ser | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 14/18 | 1818/6478 | 1710/2256 | 570/751 | chr3 | 158682103 | ||
chr3:158684541
|
C | T | 1 | a0001c0008 | 1 | NA20129.hp1 | synonymous_variant | LOW | c.1782C>T | p.Cys594Cys | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 15/18 | 1890/6478 | 1782/2256 | 594/751 | chr3 | 158684541 |
chr:pos | ref | alt | # # of thapid:transcript level |
thapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr3:158644562
|
C | T | 3 | a0001c0001t0009a0001c0001t0018a0001c0001t0036 | 8 | HG01884.hp1 HG02258.hp2 HG02622.hp2 others(5): Show |
5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-73C>T | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 1/18 | chr3 | 158644562 | ||||||
chr3:158644569
|
C | T | 1 | a0002c0002t0035 | 1 | NA20905.hp1 | 5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-66C>T | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 1/18 | chr3 | 158644569 | ||||||
chr3:158644602
|
C | T | 5 | a0001c0001t0003a0001c0001t0032a0001c0001t0034others(2): Show | 57 | HG00280.hp2 HG00423.hp1 HG00609.hp2 others(54): Show |
5_prime_UTR_variant | MODIFIER | c.-33C>T | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 1/18 | 33 | chr3 | 158644602 | |||||
chr3:158644604
|
A | G | 2 | a0001c0001t0006a0001c0001t0031 | 10 | HG00621.hp2 HG02155.hp1 HG03831.hp1 others(7): Show |
5_prime_UTR_variant | MODIFIER | c.-31A>G | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 1/18 | 31 | chr3 | 158644604 | |||||
chr3:158644624
|
C | T | 2 | a0001c0001t0011a0005c0006t0011 | 4 | HG01891.hp2 HG02055.hp1 HG02622.hp1 others(1): Show |
5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-11C>T | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 1/18 | chr3 | 158644624 | ||||||
chr3:158691473
|
C | T | 27 | a0001c0001t0003a0001c0001t0004a0001c0001t0005others(24): Show | 159 | HG00280.hp2 HG00323.hp1 HG00423.hp1 others(156): Show |
3_prime_UTR_variant | MODIFIER | c.*6C>T | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 18/18 | 6 | chr3 | 158691473 | |||||
chr3:158691583
|
C | T | 1 | a0001c0001t0030 | 1 | HG03486.hp1 | 3_prime_UTR_variant | MODIFIER | c.*116C>T | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 18/18 | 116 | chr3 | 158691583 | |||||
chr3:158691693
|
C | T | 38 | a0001c0001t0002a0001c0001t0003a0001c0001t0004others(35): Show | 233 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(230): Show |
3_prime_UTR_variant | MODIFIER | c.*226C>T | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 18/18 | 226 | chr3 | 158691693 | |||||
chr3:158691918
|
TTTG | T | 5 | a0001c0001t0003a0001c0001t0032a0001c0001t0034others(2): Show | 57 | HG00280.hp2 HG00423.hp1 HG00609.hp2 others(54): Show |
3_prime_UTR_variant | MODIFIER | c.*454_*456delGTT | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 18/18 | 454 | INFO_REALIGN_3_PRIME | chr3 | 158691918 | ||||
chr3:158691932
|
T | C | 1 | a0001c0001t0020 | 1 | NA18949.hp1 | 3_prime_UTR_variant | MODIFIER | c.*465T>C | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 18/18 | 465 | chr3 | 158691932 | |||||
chr3:158691950
|
T | TTA | 1 | a0001c0001t0005 | 9 | HG01891.hp1 HG02109.hp1 HG02145.hp2 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*483_*484insTA | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 18/18 | 484 | chr3 | 158691950 | |||||
chr3:158692006
|
C | T | 2 | a0001c0001t0017a0001c0001t0030 | 3 | HG02895.hp1 HG03130.hp1 HG03486.hp1 |
3_prime_UTR_variant | MODIFIER | c.*539C>T | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 18/18 | 539 | chr3 | 158692006 | |||||
chr3:158692135
|
T | A | 1 | a0001c0001t0021 | 1 | HG02040.hp1 | 3_prime_UTR_variant | MODIFIER | c.*668T>A | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 18/18 | 668 | chr3 | 158692135 | |||||
chr3:158692158
|
T | A | 27 | a0001c0001t0003a0001c0001t0004a0001c0001t0005others(24): Show | 159 | HG00280.hp2 HG00323.hp1 HG00423.hp1 others(156): Show |
3_prime_UTR_variant | MODIFIER | c.*691T>A | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 18/18 | 691 | chr3 | 158692158 | |||||
chr3:158692180
|
C | T | 5 | a0001c0001t0009a0001c0001t0014a0001c0001t0018others(2): Show | 12 | HG01884.hp1 HG02258.hp2 HG02622.hp2 others(9): Show |
3_prime_UTR_variant | MODIFIER | c.*713C>T | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 18/18 | 713 | chr3 | 158692180 | |||||
chr3:158692233
|
G | T | 2 | a0001c0001t0009a0001c0001t0036 | 6 | HG01884.hp1 HG02258.hp2 HG02622.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*766G>T | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 18/18 | 766 | chr3 | 158692233 | |||||
chr3:158692334
|
G | C | 1 | a0001c0004t0024 | 1 | NA18947.hp2 | 3_prime_UTR_variant | MODIFIER | c.*867G>C | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 18/18 | 867 | chr3 | 158692334 | |||||
chr3:158692335
|
T | A | 1 | a0001c0004t0024 | 1 | NA18947.hp2 | 3_prime_UTR_variant | MODIFIER | c.*868T>A | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 18/18 | 868 | chr3 | 158692335 | |||||
chr3:158692694
|
T | A | 2 | a0001c0001t0008a0001c0008t0008 | 6 | HG01884.hp2 HG02647.hp1 HG02886.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*1227T>A | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 18/18 | 1227 | chr3 | 158692694 | |||||
chr3:158692724
|
C | A | 1 | a0001c0001t0013 | 3 | NA18953.hp1 NA19004.hp2 NA19062.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1257C>A | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 18/18 | 1257 | chr3 | 158692724 | |||||
chr3:158692819
|
G | A | 1 | a0002c0002t0012 | 3 | NA18985.hp2 NA19075.hp2 NA19079.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1352G>A | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 18/18 | 1352 | chr3 | 158692819 | |||||
chr3:158692840
|
C | T | 1 | a0001c0001t0023 | 1 | HG03225.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1373C>T | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 18/18 | 1373 | chr3 | 158692840 | |||||
chr3:158693254
|
A | T | 1 | a0002c0002t0019 | 1 | NA19084.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1787A>T | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 18/18 | 1787 | chr3 | 158693254 | |||||
chr3:158693263
|
T | C | 1 | a0001c0004t0025 | 1 | HG02647.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1796T>C | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 18/18 | 1796 | chr3 | 158693263 | |||||
chr3:158693383
|
A | G | 1 | a0001c0001t0028 | 1 | HG01243.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1916A>G | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 18/18 | 1916 | chr3 | 158693383 | |||||
chr3:158693612
|
A | G | 1 | a0001c0001t0027 | 1 | HG01433.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2145A>G | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 18/18 | 2145 | chr3 | 158693612 | |||||
chr3:158693739
|
T | G | 1 | a0001c0009t0029 | 1 | HG03195.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2272T>G | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 18/18 | 2272 | chr3 | 158693739 | |||||
chr3:158693742
|
A | T | 1 | a0001c0001t0016 | 2 | NA18906.hp1 NA20300.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2275A>T | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 18/18 | 2275 | chr3 | 158693742 | |||||
chr3:158693892
|
C | T | 15 | a0001c0001t0003a0001c0001t0004a0001c0001t0008others(12): Show | 128 | HG00280.hp2 HG00323.hp1 HG00423.hp1 others(125): Show |
3_prime_UTR_variant | MODIFIER | c.*2425C>T | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 18/18 | 2425 | chr3 | 158693892 | |||||
chr3:158693915
|
G | A | 5 | a0001c0001t0003a0001c0001t0032a0001c0001t0034others(2): Show | 57 | HG00280.hp2 HG00423.hp1 HG00609.hp2 others(54): Show |
3_prime_UTR_variant | MODIFIER | c.*2448G>A | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 18/18 | 2448 | chr3 | 158693915 | |||||
chr3:158693942
|
A | G | 2 | a0001c0001t0015a0001c0001t0022 | 3 | HG03490.hp1 HG03492.hp2 HG03942.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2475A>G | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 18/18 | 2475 | chr3 | 158693942 | |||||
chr3:158693957
|
G | A | 46 | a0001c0001t0002a0001c0001t0003a0001c0001t0004others(43): Show | 368 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(365): Show |
3_prime_UTR_variant | MODIFIER | c.*2490G>A | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 18/18 | 2490 | chr3 | 158693957 | |||||
chr3:158694016
|
GT | G | 1 | a0001c0001t0005 | 9 | HG01891.hp1 HG02109.hp1 HG02145.hp2 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*2560delT | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 18/18 | 2560 | INFO_REALIGN_3_PRIME | chr3 | 158694016 | ||||
chr3:158694155
|
A | G | 1 | a0001c0001t0036 | 1 | HG02622.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2688A>G | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 18/18 | 2688 | chr3 | 158694155 | |||||
chr3:158694184
|
G | C | 1 | a0001c0001t0032 | 1 | NA18971.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2717G>C | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 18/18 | 2717 | chr3 | 158694184 | |||||
chr3:158694250
|
TA | T | 5 | a0001c0001t0003a0001c0001t0032a0001c0001t0034others(2): Show | 57 | HG00280.hp2 HG00423.hp1 HG00609.hp2 others(54): Show |
3_prime_UTR_variant | MODIFIER | c.*2790delA | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 18/18 | 2790 | INFO_REALIGN_3_PRIME | chr3 | 158694250 | ||||
chr3:158694376
|
A | G | 1 | a0001c0001t0034 | 1 | HG02300.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2909A>G | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 18/18 | 2909 | chr3 | 158694376 | |||||
chr3:158694594
|
C | T | 2 | a0001c0004t0025a0001c0004t0026 | 2 | HG01243.hp1 HG02647.hp2 |
3_prime_UTR_variant | MODIFIER | c.*3127C>T | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 18/18 | 3127 | chr3 | 158694594 | |||||
chr3:158694660
|
G | A | 1 | a0001c0001t0022 | 1 | HG03942.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3193G>A | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 18/18 | 3193 | chr3 | 158694660 | |||||
chr3:158694797
|
T | G | 1 | a0001c0001t0014 | 3 | HG03098.hp2 HG03486.hp2 NA18522.hp2 |
3_prime_UTR_variant | MODIFIER | c.*3330T>G | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 18/18 | 3330 | chr3 | 158694797 | |||||
chr3:158694852
|
GTAT | G | 1 | a0001c0001t0005 | 9 | HG01891.hp1 HG02109.hp1 HG02145.hp2 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*3390_*3392delATT | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 18/18 | 3390 | INFO_REALIGN_3_PRIME | chr3 | 158694852 | ||||
chr3:158694857
|
A | C | 1 | a0001c0001t0031 | 1 | HG03831.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3390A>C | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 18/18 | 3390 | chr3 | 158694857 | |||||
chr3:158695132
|
G | C | 1 | a0004c0005t0033 | 1 | NA18989.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3665G>C | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 18/18 | 3665 | chr3 | 158695132 | |||||
chr3:158695134
|
G | A | 1 | a0004c0005t0033 | 1 | NA18989.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3667G>A | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 18/18 | 3667 | chr3 | 158695134 | |||||
chr3:158695135
|
A | G | 1 | a0004c0005t0033 | 1 | NA18989.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3668A>G | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 18/18 | 3668 | chr3 | 158695135 | |||||
chr3:158695136
|
G | T | 1 | a0004c0005t0033 | 1 | NA18989.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3669G>T | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 18/18 | 3669 | chr3 | 158695136 | |||||
chr3:158695143
|
G | C | 1 | a0004c0005t0033 | 1 | NA18989.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3676G>C | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 18/18 | 3676 | chr3 | 158695143 | |||||
chr3:158695153
|
A | C | 38 | a0001c0001t0002a0001c0001t0003a0001c0001t0004others(35): Show | 233 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(230): Show |
3_prime_UTR_variant | MODIFIER | c.*3686A>C | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 18/18 | 3686 | chr3 | 158695153 | |||||
chr3:158695230
|
C | A | 1 | a0004c0005t0033 | 1 | NA18989.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3763C>A | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 18/18 | 3763 | chr3 | 158695230 | |||||
chr3:158695230
|
C | T | 2 | a0001c0001t0011a0005c0006t0011 | 4 | HG01891.hp2 HG02055.hp1 HG02622.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*3763C>T | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 18/18 | 3763 | chr3 | 158695230 | |||||
chr3:158695525
|
C | A | 1 | a0004c0005t0033 | 1 | NA18989.hp2 | 3_prime_UTR_variant | MODIFIER | c.*4058C>A | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 18/18 | 4058 | chr3 | 158695525 | |||||
chr3:158695532
|
A | C | 1 | a0004c0005t0033 | 1 | NA18989.hp2 | 3_prime_UTR_variant | MODIFIER | c.*4065A>C | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 18/18 | 4065 | chr3 | 158695532 |
chr:pos | ref | alt | # # of ghapid:genebody level |
ghapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | genebody_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr3:158644737
|
A | G | 142 | a0001c0001t0003g0009a0001c0001t0003g0012a0001c0001t0003g0026others(139): Show | 160 | HG00280.hp2 HG00323.hp1 HG00423.hp1 others(157): Show |
intron_variant | MODIFIER | c.81+22A>G | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 1/17 | chr3 | 158644737 | ||||||
chr3:158644779
|
A | G | 1 | a0001c0001t0023g0306 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.81+64A>G | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 1/17 | chr3 | 158644779 | ||||||
chr3:158644799
|
C | G | 142 | a0001c0001t0003g0009a0001c0001t0003g0012a0001c0001t0003g0026others(139): Show | 160 | HG00280.hp2 HG00323.hp1 HG00423.hp1 others(157): Show |
intron_variant | MODIFIER | c.81+84C>G | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 1/17 | chr3 | 158644799 | ||||||
chr3:158644874
|
A | G | 1 | a0001c0004t0026g0305 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.81+159A>G | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 1/17 | chr3 | 158644874 | ||||||
chr3:158644980
|
GT | G | 63 | a0001c0001t0002g0001a0001c0001t0002g0005a0001c0001t0002g0015others(60): Show | 76 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(73): Show |
intron_variant | MODIFIER | c.81+283delT | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr3 | 158644980 | |||||
chr3:158644980
|
GTT | G | 132 | a0001c0001t0003g0009a0001c0001t0003g0012a0001c0001t0003g0026others(129): Show | 150 | HG00280.hp2 HG00323.hp1 HG00423.hp1 others(147): Show |
intron_variant | MODIFIER | c.81+282_81+283delTT | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr3 | 158644980 | |||||
chr3:158645260
|
G | C | 1 | a0002c0002t0001g0083 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.82-369G>C | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 1/17 | chr3 | 158645260 | ||||||
chr3:158645266
|
A | C | 142 | a0001c0001t0003g0009a0001c0001t0003g0012a0001c0001t0003g0026others(139): Show | 160 | HG00280.hp2 HG00323.hp1 HG00423.hp1 others(157): Show |
intron_variant | MODIFIER | c.82-363A>C | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 1/17 | chr3 | 158645266 | ||||||
chr3:158645431
|
G | A | 2 | a0001c0001t0014g0178a0001c0001t0014g0179 | 2 | HG03486.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.82-198G>A | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 1/17 | chr3 | 158645431 | ||||||
chr3:158645511
|
A | G | 2 | a0001c0004t0025g0300a0001c0004t0026g0305 | 2 | HG01243.hp1 HG02647.hp2 |
intron_variant | MODIFIER | c.82-118A>G | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 1/17 | chr3 | 158645511 | ||||||
chr3:158645579
|
G | T | 1 | a0001c0001t0014g0179 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.82-50G>T | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 1/17 | chr3 | 158645579 | ||||||
chr3:158645800
|
T | A | 1 | a0001c0001t0004g0180 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.234+19T>A | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 2/17 | chr3 | 158645800 | ||||||
chr3:158645968
|
A | G | 12 | a0001c0001t0009g0289a0001c0001t0009g0290a0001c0001t0009g0291others(9): Show | 12 | HG01884.hp1 HG02258.hp2 HG02622.hp2 others(9): Show |
intron_variant | MODIFIER | c.234+187A>G | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 2/17 | chr3 | 158645968 | ||||||
chr3:158646080
|
G | C | 2 | a0002c0002t0001g0084a0002c0002t0001g0085 | 2 | HG02056.hp1 NA19007.hp2 |
intron_variant | MODIFIER | c.235-85G>C | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 2/17 | chr3 | 158646080 | ||||||
chr3:158646520
|
C | T | 61 | a0002c0002t0001g0007a0002c0002t0001g0008a0002c0002t0001g0011others(58): Show | 74 | HG00323.hp2 HG00558.hp1 HG00597.hp1 others(71): Show |
intron_variant | MODIFIER | c.367+223C>T | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 3/17 | chr3 | 158646520 | ||||||
chr3:158646544
|
G | A | 59 | a0001c0001t0003g0009a0001c0001t0003g0012a0001c0001t0003g0026others(56): Show | 65 | HG00280.hp2 HG00423.hp1 HG00609.hp2 others(62): Show |
intron_variant | MODIFIER | c.368-199G>A | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 3/17 | chr3 | 158646544 | ||||||
chr3:158646566
|
G | A | 2 | a0001c0001t0017g0028a0001c0001t0030g0224 | 3 | HG02895.hp1 HG03130.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.368-177G>A | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 3/17 | chr3 | 158646566 | ||||||
chr3:158646709
|
T | A | 2 | a0002c0002t0001g0086a0002c0002t0001g0087 | 2 | HG02027.hp1 HG03017.hp1 |
intron_variant | MODIFIER | c.368-34T>A | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 3/17 | chr3 | 158646709 | ||||||
chr3:158646725
|
A | G | 4 | a0001c0001t0005g0284a0001c0001t0005g0285a0001c0001t0005g0286others(1): Show | 4 | HG02109.hp1 HG02145.hp2 HG02809.hp1 others(1): Show |
intron_variant | MODIFIER | c.368-18A>G | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 3/17 | chr3 | 158646725 | ||||||
chr3:158647060
|
T | C | 1 | a0002c0002t0001g0133 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.572+113T>C | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 4/17 | chr3 | 158647060 | ||||||
chr3:158647338
|
G | A | 2 | a0001c0001t0004g0225a0001c0001t0004g0226 | 2 | HG03041.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.572+391G>A | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 4/17 | chr3 | 158647338 | ||||||
chr3:158647406
|
A | G | 1 | a0001c0004t0024g0283 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.572+459A>G | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 4/17 | chr3 | 158647406 | ||||||
chr3:158647444
|
A | T | 141 | a0001c0001t0003g0009a0001c0001t0003g0012a0001c0001t0003g0026others(138): Show | 159 | HG00280.hp2 HG00323.hp1 HG00423.hp1 others(156): Show |
intron_variant | MODIFIER | c.572+497A>T | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 4/17 | chr3 | 158647444 | ||||||
chr3:158647460
|
C | T | 1 | a0001c0004t0024g0283 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.572+513C>T | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 4/17 | chr3 | 158647460 | ||||||
chr3:158647461
|
A | G | 141 | a0001c0001t0003g0009a0001c0001t0003g0012a0001c0001t0003g0026others(138): Show | 159 | HG00280.hp2 HG00323.hp1 HG00423.hp1 others(156): Show |
intron_variant | MODIFIER | c.572+514A>G | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 4/17 | chr3 | 158647461 | ||||||
chr3:158647489
|
A | G | 8 | a0001c0001t0009g0289a0001c0001t0009g0290a0001c0001t0009g0291others(5): Show | 8 | HG01884.hp1 HG02258.hp2 HG02622.hp2 others(5): Show |
intron_variant | MODIFIER | c.572+542A>G | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 4/17 | chr3 | 158647489 | ||||||
chr3:158647513
|
C | G | 1 | a0001c0001t0023g0306 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.572+566C>G | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 4/17 | chr3 | 158647513 | ||||||
chr3:158647553
|
C | T | 1 | a0001c0001t0015g0016 | 2 | HG03490.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.572+606C>T | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 4/17 | chr3 | 158647553 | ||||||
chr3:158647660
|
T | C | 60 | a0001c0001t0002g0001a0001c0001t0002g0005a0001c0001t0002g0015others(57): Show | 73 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(70): Show |
intron_variant | MODIFIER | c.572+713T>C | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 4/17 | chr3 | 158647660 | ||||||
chr3:158647667
|
T | C | 141 | a0001c0001t0003g0009a0001c0001t0003g0012a0001c0001t0003g0026others(138): Show | 159 | HG00280.hp2 HG00323.hp1 HG00423.hp1 others(156): Show |
intron_variant | MODIFIER | c.572+720T>C | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 4/17 | chr3 | 158647667 | ||||||
chr3:158647679
|
CATTTTCT others(4): Show |
C | 1 | a0001c0001t0018g0304 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.572+733_572+743del others(11): Show |
GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 4/17 | chr3 | 158647679 | ||||||
chr3:158647692
|
G | T | 1 | a0001c0001t0018g0304 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.572+745G>T | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 4/17 | chr3 | 158647692 | ||||||
chr3:158647702
|
A | T | 1 | a0001c0001t0018g0304 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.572+755A>T | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 4/17 | chr3 | 158647702 | ||||||
chr3:158647712
|
T | G | 1 | a0001c0001t0018g0304 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.572+765T>G | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 4/17 | chr3 | 158647712 | ||||||
chr3:158647726
|
T | A | 1 | a0001c0001t0018g0304 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.572+779T>A | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 4/17 | chr3 | 158647726 | ||||||
chr3:158647727
|
A | G | 1 | a0001c0001t0018g0304 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.572+780A>G | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 4/17 | chr3 | 158647727 | ||||||
chr3:158647731
|
T | A | 1 | a0001c0001t0018g0304 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.572+784T>A | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 4/17 | chr3 | 158647731 | ||||||
chr3:158647734
|
A | G | 1 | a0001c0001t0018g0304 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.572+787A>G | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 4/17 | chr3 | 158647734 | ||||||
chr3:158647740
|
A | T | 1 | a0001c0001t0018g0304 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.572+793A>T | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 4/17 | chr3 | 158647740 | ||||||
chr3:158647749
|
A | G | 141 | a0001c0001t0003g0009a0001c0001t0003g0012a0001c0001t0003g0026others(138): Show | 159 | HG00280.hp2 HG00323.hp1 HG00423.hp1 others(156): Show |
intron_variant | MODIFIER | c.572+802A>G | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 4/17 | chr3 | 158647749 | ||||||
chr3:158647759
|
A | T | 1 | a0001c0001t0018g0304 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.572+812A>T | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 4/17 | chr3 | 158647759 | ||||||
chr3:158647761
|
A | C | 1 | a0001c0001t0018g0304 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.572+814A>C | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 4/17 | chr3 | 158647761 | ||||||
chr3:158647890
|
A | G | 1 | a0001c0001t0004g0282 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.572+943A>G | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 4/17 | chr3 | 158647890 | ||||||
chr3:158647930
|
C | T | 202 | a0001c0001t0002g0001a0001c0001t0002g0005a0001c0001t0002g0015others(199): Show | 233 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(230): Show |
intron_variant | MODIFIER | c.572+983C>T | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 4/17 | chr3 | 158647930 | ||||||
chr3:158648406
|
C | T | 9 | a0001c0001t0005g0277a0001c0001t0005g0278a0001c0001t0005g0279others(6): Show | 9 | HG01891.hp1 HG02109.hp1 HG02145.hp2 others(6): Show |
intron_variant | MODIFIER | c.573-635C>T | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 4/17 | chr3 | 158648406 | ||||||
chr3:158648411
|
G | T | 4 | a0001c0001t0002g0079a0001c0001t0002g0080a0001c0001t0002g0081others(1): Show | 4 | HG02486.hp2 HG02965.hp1 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.573-630G>T | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 4/17 | chr3 | 158648411 | ||||||
chr3:158648416
|
C | T | 141 | a0001c0001t0003g0009a0001c0001t0003g0012a0001c0001t0003g0026others(138): Show | 159 | HG00280.hp2 HG00323.hp1 HG00423.hp1 others(156): Show |
intron_variant | MODIFIER | c.573-625C>T | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 4/17 | chr3 | 158648416 | ||||||
chr3:158648417
|
A | G | 202 | a0001c0001t0002g0001a0001c0001t0002g0005a0001c0001t0002g0015others(199): Show | 233 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(230): Show |
intron_variant | MODIFIER | c.573-624A>G | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 4/17 | chr3 | 158648417 | ||||||
chr3:158648495
|
A | C | 4 | a0002c0002t0001g0010a0002c0002t0001g0018a0002c0002t0001g0132others(1): Show | 6 | HG00140.hp2 HG00639.hp1 HG01070.hp2 others(3): Show |
intron_variant | MODIFIER | c.573-546A>C | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 4/17 | chr3 | 158648495 | ||||||
chr3:158648539
|
G | T | 60 | a0001c0001t0002g0001a0001c0001t0002g0005a0001c0001t0002g0015others(57): Show | 73 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(70): Show |
intron_variant | MODIFIER | c.573-502G>T | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 4/17 | chr3 | 158648539 | ||||||
chr3:158648571
|
G | A | 2 | a0001c0001t0002g0031a0001c0001t0002g0032 | 2 | HG01123.hp2 HG01175.hp2 |
intron_variant | MODIFIER | c.573-470G>A | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 4/17 | chr3 | 158648571 | ||||||
chr3:158648625
|
C | T | 58 | a0001c0001t0004g0002a0001c0001t0004g0013a0001c0001t0004g0014others(55): Show | 69 | HG00323.hp1 HG00597.hp2 HG00642.hp2 others(66): Show |
intron_variant | MODIFIER | c.573-416C>T | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 4/17 | chr3 | 158648625 | ||||||
chr3:158648678
|
C | CA | 8 | a0002c0002t0001g0091a0002c0002t0001g0092a0002c0002t0001g0093others(5): Show | 8 | HG01074.hp2 HG01346.hp2 HG02145.hp1 others(5): Show |
intron_variant | MODIFIER | c.573-340dupA | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 4/17 | INFO_REALIGN_3_PRIME | chr3 | 158648678 | |||||
chr3:158648678
|
CA | C | 10 | a0002c0002t0001g0126a0002c0002t0001g0127a0002c0002t0001g0128others(7): Show | 10 | HG00099.hp1 HG01168.hp2 HG01175.hp1 others(7): Show |
intron_variant | MODIFIER | c.573-340delA | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 4/17 | INFO_REALIGN_3_PRIME | chr3 | 158648678 | |||||
chr3:158648678
|
CAA | C | 55 | a0001c0001t0004g0002a0001c0001t0004g0013a0001c0001t0004g0029others(52): Show | 64 | HG00597.hp2 HG00642.hp2 HG00735.hp2 others(61): Show |
intron_variant | MODIFIER | c.573-341_573-340del others(2): Show |
GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 4/17 | INFO_REALIGN_3_PRIME | chr3 | 158648678 | |||||
chr3:158648678
|
CAAA | C | 134 | a0001c0001t0002g0001a0001c0001t0002g0005a0001c0001t0002g0015others(131): Show | 156 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(153): Show |
intron_variant | MODIFIER | c.573-342_573-340del others(3): Show |
GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 4/17 | INFO_REALIGN_3_PRIME | chr3 | 158648678 | |||||
chr3:158648678
|
CAAAA | C | 12 | a0001c0001t0002g0076a0001c0001t0002g0077a0001c0001t0002g0078others(9): Show | 12 | HG01070.hp1 HG01168.hp1 HG01243.hp1 others(9): Show |
intron_variant | MODIFIER | c.573-343_573-340del others(4): Show |
GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 4/17 | INFO_REALIGN_3_PRIME | chr3 | 158648678 | |||||
chr3:158649332
|
T | TGAGAGAC others(26): Show |
1 | a0001c0001t0003g0220 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.689+175_689+176ins others(33): Show |
GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 5/17 | chr3 | 158649332 | ||||||
chr3:158649357
|
A | G | 4 | a0001c0001t0011g0227a0001c0001t0011g0228a0001c0001t0011g0229others(1): Show | 4 | HG01891.hp2 HG02055.hp1 HG02622.hp1 others(1): Show |
intron_variant | MODIFIER | c.689+200A>G | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 5/17 | chr3 | 158649357 | ||||||
chr3:158649637
|
A | G | 1 | a0001c0001t0004g0272 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.689+480A>G | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 5/17 | chr3 | 158649637 | ||||||
chr3:158649730
|
T | C | 2 | a0001c0001t0015g0016a0001c0001t0022g0033 | 3 | HG03490.hp1 HG03492.hp2 HG03942.hp2 |
intron_variant | MODIFIER | c.689+573T>C | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 5/17 | chr3 | 158649730 | ||||||
chr3:158649768
|
A | G | 60 | a0001c0001t0002g0001a0001c0001t0002g0005a0001c0001t0002g0015others(57): Show | 73 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(70): Show |
intron_variant | MODIFIER | c.689+611A>G | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 5/17 | chr3 | 158649768 | ||||||
chr3:158649809
|
G | T | 2 | a0001c0001t0003g0218a0001c0001t0003g0219 | 2 | NA18965.hp2 NA19080.hp2 |
intron_variant | MODIFIER | c.689+652G>T | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 5/17 | chr3 | 158649809 | ||||||
chr3:158650048
|
C | T | 51 | a0001c0001t0003g0009a0001c0001t0003g0012a0001c0001t0003g0026others(48): Show | 57 | HG00280.hp2 HG00423.hp1 HG00609.hp2 others(54): Show |
intron_variant | MODIFIER | c.689+891C>T | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 5/17 | chr3 | 158650048 | ||||||
chr3:158650250
|
T | C | 1 | a0001c0001t0002g0034 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.689+1093T>C | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 5/17 | chr3 | 158650250 | ||||||
chr3:158650368
|
A | C | 9 | a0001c0001t0005g0277a0001c0001t0005g0278a0001c0001t0005g0279others(6): Show | 9 | HG01891.hp1 HG02109.hp1 HG02145.hp2 others(6): Show |
intron_variant | MODIFIER | c.689+1211A>C | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 5/17 | chr3 | 158650368 | ||||||
chr3:158650428
|
G | T | 60 | a0001c0001t0002g0001a0001c0001t0002g0005a0001c0001t0002g0015others(57): Show | 73 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(70): Show |
intron_variant | MODIFIER | c.689+1271G>T | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 5/17 | chr3 | 158650428 | ||||||
chr3:158650711
|
T | G | 6 | a0001c0001t0003g0026a0001c0001t0003g0183a0001c0001t0003g0184others(3): Show | 7 | HG01070.hp1 HG01071.hp2 HG01081.hp1 others(4): Show |
intron_variant | MODIFIER | c.690-1385T>G | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 5/17 | chr3 | 158650711 | ||||||
chr3:158650735
|
A | C | 233 | a0001c0001t0002g0001a0001c0001t0002g0005a0001c0001t0002g0015others(230): Show | 268 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(265): Show |
intron_variant | MODIFIER | c.690-1361A>C | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 5/17 | chr3 | 158650735 | ||||||
chr3:158650783
|
A | G | 12 | a0002c0002t0001g0008a0002c0002t0001g0020a0002c0002t0001g0021others(9): Show | 17 | HG00558.hp1 HG00597.hp1 HG02040.hp2 others(14): Show |
intron_variant | MODIFIER | c.690-1313A>G | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 5/17 | chr3 | 158650783 | ||||||
chr3:158650808
|
G | T | 51 | a0001c0001t0003g0009a0001c0001t0003g0012a0001c0001t0003g0026others(48): Show | 57 | HG00280.hp2 HG00423.hp1 HG00609.hp2 others(54): Show |
intron_variant | MODIFIER | c.690-1288G>T | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 5/17 | chr3 | 158650808 | ||||||
chr3:158650838
|
C | T | 1 | a0001c0001t0002g0075 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.690-1258C>T | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 5/17 | chr3 | 158650838 | ||||||
chr3:158650995
|
T | C | 141 | a0001c0001t0003g0009a0001c0001t0003g0012a0001c0001t0003g0026others(138): Show | 159 | HG00280.hp2 HG00323.hp1 HG00423.hp1 others(156): Show |
intron_variant | MODIFIER | c.690-1101T>C | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 5/17 | chr3 | 158650995 | ||||||
chr3:158651012
|
C | G | 60 | a0001c0001t0002g0001a0001c0001t0002g0005a0001c0001t0002g0015others(57): Show | 73 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(70): Show |
intron_variant | MODIFIER | c.690-1084C>G | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 5/17 | chr3 | 158651012 | ||||||
chr3:158651020
|
C | CA | 81 | a0001c0001t0002g0034a0001c0001t0002g0039a0001c0001t0002g0040others(78): Show | 85 | HG00140.hp1 HG00280.hp2 HG00423.hp1 others(82): Show |
intron_variant | MODIFIER | c.690-1051dupA | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 5/17 | INFO_REALIGN_3_PRIME | chr3 | 158651020 | |||||
chr3:158651020
|
C | CAA | 20 | a0001c0001t0002g0035a0001c0001t0003g0186a0001c0001t0003g0218others(17): Show | 20 | HG01243.hp1 HG01884.hp2 HG01891.hp2 others(17): Show |
intron_variant | MODIFIER | c.690-1052_690-1051d others(4): Show |
GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 5/17 | INFO_REALIGN_3_PRIME | chr3 | 158651020 | |||||
chr3:158651020
|
C | CAAA | 47 | a0001c0001t0004g0002a0001c0001t0004g0013a0001c0001t0004g0014others(44): Show | 58 | HG00323.hp1 HG00642.hp2 HG00735.hp2 others(55): Show |
intron_variant | MODIFIER | c.690-1053_690-1051d others(5): Show |
GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 5/17 | INFO_REALIGN_3_PRIME | chr3 | 158651020 | |||||
chr3:158651020
|
C | CAAAA | 7 | a0001c0001t0004g0231a0001c0001t0004g0232a0001c0001t0004g0233others(4): Show | 7 | HG00597.hp2 HG01175.hp1 HG02257.hp1 others(4): Show |
intron_variant | MODIFIER | c.690-1054_690-1051d others(6): Show |
GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 5/17 | INFO_REALIGN_3_PRIME | chr3 | 158651020 | |||||
chr3:158651020
|
CAAAAAAA others(3): Show |
C | 5 | a0001c0001t0003g0012a0001c0001t0003g0027a0001c0001t0003g0215others(2): Show | 8 | HG02056.hp2 HG02129.hp1 HG02135.hp2 others(5): Show |
intron_variant | MODIFIER | c.690-1060_690-1051d others(12): Show |
GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 5/17 | INFO_REALIGN_3_PRIME | chr3 | 158651020 | |||||
chr3:158651142
|
C | T | 3 | a0001c0004t0024g0283a0001c0004t0025g0300a0001c0004t0026g0305 | 3 | HG01243.hp1 HG02647.hp2 NA18947.hp2 |
intron_variant | MODIFIER | c.690-954C>T | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 5/17 | chr3 | 158651142 | ||||||
chr3:158651161
|
C | G | 2 | a0001c0001t0003g0213a0001c0001t0003g0214 | 2 | NA18954.hp1 NA18974.hp1 |
intron_variant | MODIFIER | c.690-935C>G | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 5/17 | chr3 | 158651161 | ||||||
chr3:158651178
|
A | G | 4 | a0001c0001t0011g0227a0001c0001t0011g0228a0001c0001t0011g0229others(1): Show | 4 | HG01891.hp2 HG02055.hp1 HG02622.hp1 others(1): Show |
intron_variant | MODIFIER | c.690-918A>G | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 5/17 | chr3 | 158651178 | ||||||
chr3:158651212
|
C | G | 1 | a0003c0003t0007g0235 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.690-884C>G | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 5/17 | chr3 | 158651212 | ||||||
chr3:158651284
|
G | A | 1 | a0001c0001t0002g0043 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.690-812G>A | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 5/17 | chr3 | 158651284 | ||||||
chr3:158651313
|
T | G | 9 | a0001c0001t0005g0277a0001c0001t0005g0278a0001c0001t0005g0279others(6): Show | 9 | HG01891.hp1 HG02109.hp1 HG02145.hp2 others(6): Show |
intron_variant | MODIFIER | c.690-783T>G | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 5/17 | chr3 | 158651313 | ||||||
chr3:158651371
|
T | C | 141 | a0001c0001t0003g0009a0001c0001t0003g0012a0001c0001t0003g0026others(138): Show | 159 | HG00280.hp2 HG00323.hp1 HG00423.hp1 others(156): Show |
intron_variant | MODIFIER | c.690-725T>C | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 5/17 | chr3 | 158651371 | ||||||
chr3:158651374
|
G | A | 141 | a0001c0001t0003g0009a0001c0001t0003g0012a0001c0001t0003g0026others(138): Show | 159 | HG00280.hp2 HG00323.hp1 HG00423.hp1 others(156): Show |
intron_variant | MODIFIER | c.690-722G>A | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 5/17 | chr3 | 158651374 | ||||||
chr3:158651640
|
A | T | 9 | a0001c0001t0005g0277a0001c0001t0005g0278a0001c0001t0005g0279others(6): Show | 9 | HG01891.hp1 HG02109.hp1 HG02145.hp2 others(6): Show |
intron_variant | MODIFIER | c.690-456A>T | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 5/17 | chr3 | 158651640 | ||||||
chr3:158651663
|
T | C | 141 | a0001c0001t0003g0009a0001c0001t0003g0012a0001c0001t0003g0026others(138): Show | 159 | HG00280.hp2 HG00323.hp1 HG00423.hp1 others(156): Show |
intron_variant | MODIFIER | c.690-433T>C | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 5/17 | chr3 | 158651663 | ||||||
chr3:158651781
|
A | C | 1 | a0001c0001t0002g0074 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.690-315A>C | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 5/17 | chr3 | 158651781 | ||||||
chr3:158651824
|
AT | A | 142 | a0001c0001t0003g0009a0001c0001t0003g0012a0001c0001t0003g0026others(139): Show | 160 | HG00280.hp2 HG00323.hp1 HG00423.hp1 others(157): Show |
intron_variant | MODIFIER | c.690-262delT | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 5/17 | INFO_REALIGN_3_PRIME | chr3 | 158651824 | |||||
chr3:158652000
|
T | A | 51 | a0001c0001t0003g0009a0001c0001t0003g0012a0001c0001t0003g0026others(48): Show | 57 | HG00280.hp2 HG00423.hp1 HG00609.hp2 others(54): Show |
intron_variant | MODIFIER | c.690-96T>A | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 5/17 | chr3 | 158652000 | ||||||
chr3:158652009
|
A | G | 141 | a0001c0001t0003g0009a0001c0001t0003g0012a0001c0001t0003g0026others(138): Show | 159 | HG00280.hp2 HG00323.hp1 HG00423.hp1 others(156): Show |
intron_variant | MODIFIER | c.690-87A>G | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 5/17 | chr3 | 158652009 | ||||||
chr3:158652056
|
G | A | 5 | a0001c0001t0002g0044a0001c0001t0002g0045a0001c0001t0002g0046others(2): Show | 5 | NA18939.hp2 NA18962.hp2 NA18967.hp2 others(2): Show |
intron_variant | MODIFIER | c.690-40G>A | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 5/17 | chr3 | 158652056 | ||||||
chr3:158652335
|
G | C | 1 | a0001c0001t0027g0236 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.840+89G>C | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 6/17 | chr3 | 158652335 | ||||||
chr3:158652338
|
T | C | 6 | a0001c0001t0009g0289a0001c0001t0009g0290a0001c0001t0009g0291others(3): Show | 6 | HG01884.hp1 HG02258.hp2 HG02622.hp2 others(3): Show |
intron_variant | MODIFIER | c.840+92T>C | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 6/17 | chr3 | 158652338 | ||||||
chr3:158652354
|
C | G | 2 | a0002c0002t0001g0019a0002c0002t0001g0149 | 3 | HG03239.hp2 HG03704.hp1 NA20805.hp1 |
intron_variant | MODIFIER | c.840+108C>G | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 6/17 | chr3 | 158652354 | ||||||
chr3:158652429
|
T | C | 1 | a0001c0001t0003g0187 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.840+183T>C | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 6/17 | chr3 | 158652429 | ||||||
chr3:158652563
|
T | C | 2 | a0001c0001t0017g0028a0001c0001t0030g0224 | 3 | HG02895.hp1 HG03130.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.840+317T>C | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 6/17 | chr3 | 158652563 | ||||||
chr3:158652754
|
A | T | 141 | a0001c0001t0003g0009a0001c0001t0003g0012a0001c0001t0003g0026others(138): Show | 159 | HG00280.hp2 HG00323.hp1 HG00423.hp1 others(156): Show |
intron_variant | MODIFIER | c.840+508A>T | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 6/17 | chr3 | 158652754 | ||||||
chr3:158652898
|
C | T | 1 | a0001c0001t0005g0284 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.841-412C>T | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 6/17 | chr3 | 158652898 | ||||||
chr3:158652945
|
G | A | 141 | a0001c0001t0003g0009a0001c0001t0003g0012a0001c0001t0003g0026others(138): Show | 159 | HG00280.hp2 HG00323.hp1 HG00423.hp1 others(156): Show |
intron_variant | MODIFIER | c.841-365G>A | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 6/17 | chr3 | 158652945 | ||||||
chr3:158652983
|
C | T | 3 | a0001c0001t0014g0178a0001c0001t0014g0179a0001c0001t0014g0296 | 3 | HG03098.hp2 HG03486.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.841-327C>T | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 6/17 | chr3 | 158652983 | ||||||
chr3:158653014
|
T | C | 1 | a0011c0011t0004g0299 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.841-296T>C | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 6/17 | chr3 | 158653014 | ||||||
chr3:158653086
|
C | T | 51 | a0001c0001t0003g0009a0001c0001t0003g0012a0001c0001t0003g0026others(48): Show | 57 | HG00280.hp2 HG00423.hp1 HG00609.hp2 others(54): Show |
intron_variant | MODIFIER | c.841-224C>T | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 6/17 | chr3 | 158653086 | ||||||
chr3:158653198
|
C | T | 1 | a0002c0002t0001g0177 | 1 | NA18951.hp1 | intron_variant | MODIFIER | c.841-112C>T | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 6/17 | chr3 | 158653198 | ||||||
chr3:158653617
|
G | A | 141 | a0001c0001t0003g0009a0001c0001t0003g0012a0001c0001t0003g0026others(138): Show | 159 | HG00280.hp2 HG00323.hp1 HG00423.hp1 others(156): Show |
intron_variant | MODIFIER | c.998+150G>A | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 7/17 | chr3 | 158653617 | ||||||
chr3:158653757
|
T | TA | 136 | a0001c0001t0003g0009a0001c0001t0003g0012a0001c0001t0003g0026others(133): Show | 154 | HG00280.hp2 HG00323.hp1 HG00423.hp1 others(151): Show |
intron_variant | MODIFIER | c.998+302dupA | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 7/17 | INFO_REALIGN_3_PRIME | chr3 | 158653757 | |||||
chr3:158653846
|
G | A | 141 | a0001c0001t0003g0009a0001c0001t0003g0012a0001c0001t0003g0026others(138): Show | 159 | HG00280.hp2 HG00323.hp1 HG00423.hp1 others(156): Show |
intron_variant | MODIFIER | c.998+379G>A | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 7/17 | chr3 | 158653846 | ||||||
chr3:158653978
|
G | C | 1 | a0001c0001t0004g0225 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.998+511G>C | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 7/17 | chr3 | 158653978 | ||||||
chr3:158654066
|
A | T | 1 | a0001c0001t0004g0265 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.999-481A>T | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 7/17 | chr3 | 158654066 | ||||||
chr3:158654204
|
C | T | 1 | a0002c0002t0001g0125 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.999-343C>T | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 7/17 | chr3 | 158654204 | ||||||
chr3:158654205
|
C | CT | 94 | a0001c0001t0002g0001a0001c0001t0002g0005a0001c0001t0002g0015others(91): Show | 114 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(111): Show |
intron_variant | MODIFIER | c.999-318dupT | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 7/17 | INFO_REALIGN_3_PRIME | chr3 | 158654205 | |||||
chr3:158654205
|
C | CTT | 78 | a0001c0001t0002g0032a0001c0001t0002g0042a0001c0001t0002g0046others(75): Show | 88 | HG00323.hp1 HG00423.hp1 HG00423.hp2 others(85): Show |
intron_variant | MODIFIER | c.999-319_999-318dup others(2): Show |
GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 7/17 | INFO_REALIGN_3_PRIME | chr3 | 158654205 | |||||
chr3:158654205
|
C | CTTT | 24 | a0001c0001t0003g0212a0001c0001t0004g0013a0001c0001t0004g0030others(21): Show | 26 | HG00642.hp2 HG00735.hp2 HG01891.hp1 others(23): Show |
intron_variant | MODIFIER | c.999-320_999-318dup others(3): Show |
GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 7/17 | INFO_REALIGN_3_PRIME | chr3 | 158654205 | |||||
chr3:158654205
|
C | CTTTT | 6 | a0001c0001t0005g0281a0001c0001t0005g0284a0001c0001t0011g0228others(3): Show | 6 | HG01243.hp1 HG01243.hp2 HG02055.hp1 others(3): Show |
intron_variant | MODIFIER | c.999-321_999-318dup others(4): Show |
GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 7/17 | INFO_REALIGN_3_PRIME | chr3 | 158654205 | |||||
chr3:158654300
|
A | G | 4 | a0001c0001t0014g0178a0001c0001t0014g0179a0001c0001t0014g0296others(1): Show | 4 | HG03098.hp2 HG03195.hp2 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.999-247A>G | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 7/17 | chr3 | 158654300 | ||||||
chr3:158654326
|
A | T | 4 | a0001c0001t0011g0227a0001c0001t0011g0228a0001c0001t0011g0229others(1): Show | 4 | HG01891.hp2 HG02055.hp1 HG02622.hp1 others(1): Show |
intron_variant | MODIFIER | c.999-221A>T | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 7/17 | chr3 | 158654326 | ||||||
chr3:158654436
|
A | G | 1 | a0001c0001t0004g0258 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.999-111A>G | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 7/17 | chr3 | 158654436 | ||||||
chr3:158654454
|
T | A | 1 | a0001c0001t0003g0297 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.999-93T>A | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 7/17 | chr3 | 158654454 | ||||||
chr3:158654637
|
T | G | 1 | a0001c0001t0003g0220 | 1 | HG00280.hp2 | splice_region_variant&intron_variant | LOW | c.1083+6T>G | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 8/17 | chr3 | 158654637 | ||||||
chr3:158654688
|
C | T | 119 | a0001c0001t0003g0009a0001c0001t0003g0012a0001c0001t0003g0026others(116): Show | 136 | HG00280.hp2 HG00323.hp1 HG00423.hp1 others(133): Show |
intron_variant | MODIFIER | c.1083+57C>T | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 8/17 | chr3 | 158654688 | ||||||
chr3:158654713
|
T | C | 141 | a0001c0001t0003g0009a0001c0001t0003g0012a0001c0001t0003g0026others(138): Show | 159 | HG00280.hp2 HG00323.hp1 HG00423.hp1 others(156): Show |
intron_variant | MODIFIER | c.1083+82T>C | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 8/17 | chr3 | 158654713 | ||||||
chr3:158654886
|
G | T | 2 | a0001c0001t0004g0233a0001c0001t0004g0257 | 2 | HG02257.hp1 HG02630.hp1 |
intron_variant | MODIFIER | c.1083+255G>T | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 8/17 | chr3 | 158654886 | ||||||
chr3:158655141
|
A | G | 142 | a0001c0001t0002g0045a0001c0001t0003g0009a0001c0001t0003g0012others(139): Show | 160 | HG00280.hp2 HG00323.hp1 HG00423.hp1 others(157): Show |
intron_variant | MODIFIER | c.1083+510A>G | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 8/17 | chr3 | 158655141 | ||||||
chr3:158655156
|
T | C | 1 | a0001c0001t0009g0289 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.1083+525T>C | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 8/17 | chr3 | 158655156 | ||||||
chr3:158655168
|
A | G | 9 | a0001c0001t0005g0277a0001c0001t0005g0278a0001c0001t0005g0279others(6): Show | 9 | HG01891.hp1 HG02109.hp1 HG02145.hp2 others(6): Show |
intron_variant | MODIFIER | c.1083+537A>G | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 8/17 | chr3 | 158655168 | ||||||
chr3:158655207
|
T | A | 60 | a0001c0001t0002g0001a0001c0001t0002g0005a0001c0001t0002g0015others(57): Show | 73 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(70): Show |
intron_variant | MODIFIER | c.1083+576T>A | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 8/17 | chr3 | 158655207 | ||||||
chr3:158655249
|
G | A | 2 | a0001c0004t0025g0300a0001c0004t0026g0305 | 2 | HG01243.hp1 HG02647.hp2 |
intron_variant | MODIFIER | c.1083+618G>A | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 8/17 | chr3 | 158655249 | ||||||
chr3:158655260
|
C | T | 4 | a0001c0004t0024g0283a0002c0002t0001g0086a0002c0002t0001g0087others(1): Show | 4 | HG02027.hp1 HG03017.hp1 HG04115.hp2 others(1): Show |
intron_variant | MODIFIER | c.1083+629C>T | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 8/17 | chr3 | 158655260 | ||||||
chr3:158655275
|
G | T | 2 | a0002c0002t0001g0097a0009c0014t0001g0094 | 2 | HG02109.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.1083+644G>T | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 8/17 | chr3 | 158655275 | ||||||
chr3:158655300
|
A | G | 1 | a0001c0001t0004g0256 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.1083+669A>G | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 8/17 | chr3 | 158655300 | ||||||
chr3:158655310
|
C | A | 2 | a0001c0001t0003g0027a0001c0001t0003g0215 | 3 | HG02129.hp1 HG03831.hp2 NA19070.hp1 |
intron_variant | MODIFIER | c.1083+679C>A | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 8/17 | chr3 | 158655310 | ||||||
chr3:158655408
|
T | C | 143 | a0001c0001t0003g0009a0001c0001t0003g0012a0001c0001t0003g0026others(140): Show | 161 | HG00280.hp2 HG00323.hp1 HG00423.hp1 others(158): Show |
intron_variant | MODIFIER | c.1083+777T>C | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 8/17 | chr3 | 158655408 | ||||||
chr3:158655466
|
A | T | 1 | a0001c0001t0002g0041 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.1083+835A>T | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 8/17 | chr3 | 158655466 | ||||||
chr3:158655485
|
G | GA | 142 | a0001c0001t0003g0009a0001c0001t0003g0012a0001c0001t0003g0026others(139): Show | 160 | HG00280.hp2 HG00323.hp1 HG00423.hp1 others(157): Show |
intron_variant | MODIFIER | c.1083+867dupA | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 8/17 | INFO_REALIGN_3_PRIME | chr3 | 158655485 | |||||
chr3:158655670
|
T | C | 141 | a0001c0001t0003g0009a0001c0001t0003g0012a0001c0001t0003g0026others(138): Show | 159 | HG00280.hp2 HG00323.hp1 HG00423.hp1 others(156): Show |
intron_variant | MODIFIER | c.1083+1039T>C | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 8/17 | chr3 | 158655670 | ||||||
chr3:158655761
|
T | C | 60 | a0001c0001t0004g0002a0001c0001t0004g0013a0001c0001t0004g0014others(57): Show | 71 | HG00323.hp1 HG00597.hp2 HG00642.hp2 others(68): Show |
intron_variant | MODIFIER | c.1083+1130T>C | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 8/17 | chr3 | 158655761 | ||||||
chr3:158655872
|
C | A | 1 | a0001c0001t0023g0306 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.1083+1241C>A | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 8/17 | chr3 | 158655872 | ||||||
chr3:158655946
|
C | T | 1 | a0001c0001t0003g0211 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.1083+1315C>T | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 8/17 | chr3 | 158655946 | ||||||
chr3:158656040
|
G | A | 1 | a0001c0001t0002g0050 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.1083+1409G>A | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 8/17 | chr3 | 158656040 | ||||||
chr3:158656141
|
GT | G | 200 | a0001c0001t0002g0001a0001c0001t0002g0005a0001c0001t0002g0015others(197): Show | 231 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(228): Show |
intron_variant | MODIFIER | c.1083+1519delT | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 8/17 | INFO_REALIGN_3_PRIME | chr3 | 158656141 | |||||
chr3:158656227
|
C | T | 1 | a0002c0002t0001g0119 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.1083+1596C>T | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 8/17 | chr3 | 158656227 | ||||||
chr3:158656228
|
G | A | 202 | a0001c0001t0002g0001a0001c0001t0002g0005a0001c0001t0002g0015others(199): Show | 233 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(230): Show |
intron_variant | MODIFIER | c.1083+1597G>A | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 8/17 | chr3 | 158656228 | ||||||
chr3:158656230
|
T | A | 9 | a0001c0001t0005g0277a0001c0001t0005g0278a0001c0001t0005g0279others(6): Show | 9 | HG01891.hp1 HG02109.hp1 HG02145.hp2 others(6): Show |
intron_variant | MODIFIER | c.1083+1599T>A | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 8/17 | chr3 | 158656230 | ||||||
chr3:158656342
|
A | G | 202 | a0001c0001t0002g0001a0001c0001t0002g0005a0001c0001t0002g0015others(199): Show | 233 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(230): Show |
intron_variant | MODIFIER | c.1083+1711A>G | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 8/17 | chr3 | 158656342 | ||||||
chr3:158656372
|
C | T | 1 | a0001c0001t0002g0065 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.1083+1741C>T | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 8/17 | chr3 | 158656372 | ||||||
chr3:158656427
|
A | G | 1 | a0002c0002t0001g0118 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.1083+1796A>G | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 8/17 | chr3 | 158656427 | ||||||
chr3:158656433
|
A | G | 141 | a0001c0001t0003g0009a0001c0001t0003g0012a0001c0001t0003g0026others(138): Show | 159 | HG00280.hp2 HG00323.hp1 HG00423.hp1 others(156): Show |
intron_variant | MODIFIER | c.1083+1802A>G | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 8/17 | chr3 | 158656433 | ||||||
chr3:158656602
|
T | TAAG | 202 | a0001c0001t0002g0001a0001c0001t0002g0005a0001c0001t0002g0015others(199): Show | 233 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(230): Show |
intron_variant | MODIFIER | c.1083+1971_1083+197 others(7): Show |
GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 8/17 | chr3 | 158656602 | ||||||
chr3:158656700
|
A | G | 2 | a0001c0001t0017g0028a0001c0001t0030g0224 | 3 | HG02895.hp1 HG03130.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.1083+2069A>G | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 8/17 | chr3 | 158656700 | ||||||
chr3:158656737
|
G | A | 1 | a0001c0001t0004g0272 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.1083+2106G>A | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 8/17 | chr3 | 158656737 | ||||||
chr3:158656746
|
C | G | 60 | a0001c0001t0002g0001a0001c0001t0002g0005a0001c0001t0002g0015others(57): Show | 73 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(70): Show |
intron_variant | MODIFIER | c.1083+2115C>G | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 8/17 | chr3 | 158656746 | ||||||
chr3:158656911
|
C | T | 4 | a0002c0002t0001g0171a0002c0002t0001g0172a0002c0002t0001g0173others(1): Show | 4 | HG01081.hp2 NA18956.hp2 NA18965.hp1 others(1): Show |
intron_variant | MODIFIER | c.1084-2011C>T | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 8/17 | chr3 | 158656911 | ||||||
chr3:158656917
|
G | A | 1 | a0001c0001t0003g0189 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.1084-2005G>A | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 8/17 | chr3 | 158656917 | ||||||
chr3:158656920
|
T | C | 202 | a0001c0001t0002g0001a0001c0001t0002g0005a0001c0001t0002g0015others(199): Show | 233 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(230): Show |
intron_variant | MODIFIER | c.1084-2002T>C | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 8/17 | chr3 | 158656920 | ||||||
chr3:158657035
|
G | A | 1 | a0001c0004t0024g0283 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.1084-1887G>A | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 8/17 | chr3 | 158657035 | ||||||
chr3:158657077
|
A | C | 1 | a0001c0001t0003g0186 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1084-1845A>C | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 8/17 | chr3 | 158657077 | ||||||
chr3:158657209
|
A | T | 4 | a0001c0001t0014g0178a0001c0001t0014g0179a0001c0001t0014g0296others(1): Show | 4 | HG03098.hp2 HG03195.hp2 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.1084-1713A>T | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 8/17 | chr3 | 158657209 | ||||||
chr3:158657251
|
A | T | 141 | a0001c0001t0003g0009a0001c0001t0003g0012a0001c0001t0003g0026others(138): Show | 159 | HG00280.hp2 HG00323.hp1 HG00423.hp1 others(156): Show |
intron_variant | MODIFIER | c.1084-1671A>T | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 8/17 | chr3 | 158657251 | ||||||
chr3:158657288
|
A | T | 1 | a0001c0001t0003g0210 | 1 | NA19089.hp1 | intron_variant | MODIFIER | c.1084-1634A>T | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 8/17 | chr3 | 158657288 | ||||||
chr3:158657290
|
AT | A | 60 | a0001c0001t0002g0001a0001c0001t0002g0005a0001c0001t0002g0015others(57): Show | 73 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(70): Show |
intron_variant | MODIFIER | c.1084-1628delT | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 8/17 | INFO_REALIGN_3_PRIME | chr3 | 158657290 | |||||
chr3:158657634
|
G | A | 2 | a0001c0001t0004g0225a0001c0001t0004g0226 | 2 | HG03041.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.1084-1288G>A | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 8/17 | chr3 | 158657634 | ||||||
chr3:158657654
|
T | G | 1 | a0001c0001t0023g0306 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.1084-1268T>G | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 8/17 | chr3 | 158657654 | ||||||
chr3:158657840
|
T | C | 1 | a0002c0002t0001g0100 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.1084-1082T>C | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 8/17 | chr3 | 158657840 | ||||||
chr3:158657869
|
T | C | 1 | a0001c0001t0023g0306 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.1084-1053T>C | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 8/17 | chr3 | 158657869 | ||||||
chr3:158657999
|
C | T | 141 | a0001c0001t0003g0009a0001c0001t0003g0012a0001c0001t0003g0026others(138): Show | 159 | HG00280.hp2 HG00323.hp1 HG00423.hp1 others(156): Show |
intron_variant | MODIFIER | c.1084-923C>T | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 8/17 | chr3 | 158657999 | ||||||
chr3:158658054
|
G | A | 1 | a0001c0001t0023g0306 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.1084-868G>A | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 8/17 | chr3 | 158658054 | ||||||
chr3:158658157
|
C | CT | 6 | a0002c0002t0001g0083a0002c0002t0001g0096a0002c0002t0001g0098others(3): Show | 6 | HG01978.hp2 HG02055.hp2 HG04115.hp1 others(3): Show |
intron_variant | MODIFIER | c.1084-742dupT | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 8/17 | INFO_REALIGN_3_PRIME | chr3 | 158658157 | |||||
chr3:158658157
|
C | CTTT | 46 | a0001c0001t0004g0029a0001c0001t0004g0233a0001c0001t0004g0245others(43): Show | 47 | HG01175.hp1 HG01243.hp1 HG01884.hp1 others(44): Show |
intron_variant | MODIFIER | c.1084-744_1084-742d others(5): Show |
GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 8/17 | INFO_REALIGN_3_PRIME | chr3 | 158658157 | |||||
chr3:158658157
|
C | CTTTT | 17 | a0001c0001t0003g0190a0001c0001t0003g0213a0001c0001t0003g0223others(14): Show | 18 | HG01243.hp2 HG01891.hp2 HG02055.hp1 others(15): Show |
intron_variant | MODIFIER | c.1084-745_1084-742d others(6): Show |
GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 8/17 | INFO_REALIGN_3_PRIME | chr3 | 158658157 | |||||
chr3:158658157
|
C | CTTTTT | 28 | a0001c0001t0003g0009a0001c0001t0003g0012a0001c0001t0003g0027others(25): Show | 33 | HG00280.hp2 HG00609.hp2 HG01069.hp2 others(30): Show |
intron_variant | MODIFIER | c.1084-746_1084-742d others(7): Show |
GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 8/17 | INFO_REALIGN_3_PRIME | chr3 | 158658157 | |||||
chr3:158658157
|
C | CTTTTTT | 18 | a0001c0001t0003g0026a0001c0001t0003g0183a0001c0001t0003g0184others(15): Show | 19 | HG01070.hp1 HG01071.hp2 HG01081.hp1 others(16): Show |
intron_variant | MODIFIER | c.1084-747_1084-742d others(8): Show |
GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 8/17 | INFO_REALIGN_3_PRIME | chr3 | 158658157 | |||||
chr3:158658157
|
CT | C | 11 | a0001c0001t0002g0040a0001c0001t0002g0047a0001c0001t0002g0079others(8): Show | 11 | HG01081.hp2 HG01168.hp2 HG01515.hp2 others(8): Show |
intron_variant | MODIFIER | c.1084-742delT | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 8/17 | INFO_REALIGN_3_PRIME | chr3 | 158658157 | |||||
chr3:158658157
|
CTT | C | 52 | a0001c0001t0002g0001a0001c0001t0002g0005a0001c0001t0002g0015others(49): Show | 65 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(62): Show |
intron_variant | MODIFIER | c.1084-743_1084-742d others(4): Show |
GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 8/17 | INFO_REALIGN_3_PRIME | chr3 | 158658157 | |||||
chr3:158658157
|
CTTTT | C | 28 | a0001c0001t0004g0002a0001c0001t0004g0013a0001c0001t0004g0014others(25): Show | 38 | HG00323.hp1 HG00597.hp2 HG00642.hp2 others(35): Show |
intron_variant | MODIFIER | c.1084-745_1084-742d others(6): Show |
GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 8/17 | INFO_REALIGN_3_PRIME | chr3 | 158658157 | |||||
chr3:158658215
|
G | A | 3 | a0002c0002t0001g0086a0002c0002t0001g0087a0002c0002t0001g0124 | 3 | HG02027.hp1 HG03017.hp1 HG04115.hp2 |
intron_variant | MODIFIER | c.1084-707G>A | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 8/17 | chr3 | 158658215 | ||||||
chr3:158658367
|
G | C | 60 | a0001c0001t0004g0002a0001c0001t0004g0013a0001c0001t0004g0014others(57): Show | 71 | HG00323.hp1 HG00597.hp2 HG00642.hp2 others(68): Show |
intron_variant | MODIFIER | c.1084-555G>C | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 8/17 | chr3 | 158658367 | ||||||
chr3:158658411
|
C | T | 1 | a0001c0004t0024g0283 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.1084-511C>T | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 8/17 | chr3 | 158658411 | ||||||
chr3:158658565
|
C | G | 51 | a0001c0001t0003g0009a0001c0001t0003g0012a0001c0001t0003g0026others(48): Show | 57 | HG00280.hp2 HG00423.hp1 HG00609.hp2 others(54): Show |
intron_variant | MODIFIER | c.1084-357C>G | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 8/17 | chr3 | 158658565 | ||||||
chr3:158658866
|
T | A | 1 | a0001c0001t0002g0042 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.1084-56T>A | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 8/17 | chr3 | 158658866 | ||||||
chr3:158659162
|
A | G | 1 | a0001c0001t0013g0275 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.1221+103A>G | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 9/17 | chr3 | 158659162 | ||||||
chr3:158659262
|
G | A | 2 | a0001c0001t0018g0294a0001c0001t0018g0304 | 2 | HG02723.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.1221+203G>A | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 9/17 | chr3 | 158659262 | ||||||
chr3:158659281
|
T | C | 1 | a0001c0001t0023g0306 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.1221+222T>C | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 9/17 | chr3 | 158659281 | ||||||
chr3:158659352
|
C | A | 1 | a0001c0001t0004g0257 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.1221+293C>A | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 9/17 | chr3 | 158659352 | ||||||
chr3:158659382
|
T | C | 1 | a0001c0009t0029g0295 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.1221+323T>C | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 9/17 | chr3 | 158659382 | ||||||
chr3:158659513
|
T | C | 1 | a0002c0002t0001g0138 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.1221+454T>C | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 9/17 | chr3 | 158659513 | ||||||
chr3:158659653
|
C | G | 1 | a0001c0004t0024g0283 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.1221+594C>G | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 9/17 | chr3 | 158659653 | ||||||
chr3:158659681
|
G | A | 60 | a0001c0001t0002g0001a0001c0001t0002g0005a0001c0001t0002g0015others(57): Show | 73 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(70): Show |
intron_variant | MODIFIER | c.1221+622G>A | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 9/17 | chr3 | 158659681 | ||||||
chr3:158659695
|
T | G | 4 | a0002c0002t0001g0171a0002c0002t0001g0172a0002c0002t0001g0173others(1): Show | 4 | HG01081.hp2 NA18956.hp2 NA18965.hp1 others(1): Show |
intron_variant | MODIFIER | c.1221+636T>G | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 9/17 | chr3 | 158659695 | ||||||
chr3:158659702
|
A | G | 126 | a0001c0001t0003g0009a0001c0001t0003g0012a0001c0001t0003g0026others(123): Show | 143 | HG00280.hp2 HG00323.hp1 HG00423.hp1 others(140): Show |
intron_variant | MODIFIER | c.1221+643A>G | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 9/17 | chr3 | 158659702 | ||||||
chr3:158659765
|
G | T | 202 | a0001c0001t0002g0001a0001c0001t0002g0005a0001c0001t0002g0015others(199): Show | 233 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(230): Show |
intron_variant | MODIFIER | c.1221+706G>T | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 9/17 | chr3 | 158659765 | ||||||
chr3:158659780
|
C | T | 9 | a0001c0001t0005g0277a0001c0001t0005g0278a0001c0001t0005g0279others(6): Show | 9 | HG01891.hp1 HG02109.hp1 HG02145.hp2 others(6): Show |
intron_variant | MODIFIER | c.1221+721C>T | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 9/17 | chr3 | 158659780 | ||||||
chr3:158659877
|
G | T | 2 | a0001c0004t0025g0300a0001c0004t0026g0305 | 2 | HG01243.hp1 HG02647.hp2 |
intron_variant | MODIFIER | c.1221+818G>T | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 9/17 | chr3 | 158659877 | ||||||
chr3:158660008
|
C | G | 201 | a0001c0001t0002g0001a0001c0001t0002g0005a0001c0001t0002g0015others(198): Show | 232 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(229): Show |
intron_variant | MODIFIER | c.1222-866C>G | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 9/17 | chr3 | 158660008 | ||||||
chr3:158660124
|
C | T | 60 | a0001c0001t0002g0001a0001c0001t0002g0005a0001c0001t0002g0015others(57): Show | 73 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(70): Show |
intron_variant | MODIFIER | c.1222-750C>T | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 9/17 | chr3 | 158660124 | ||||||
chr3:158660248
|
C | CT | 79 | a0001c0001t0002g0032a0001c0001t0003g0009a0001c0001t0003g0012others(76): Show | 86 | HG00280.hp2 HG00423.hp1 HG00609.hp2 others(83): Show |
intron_variant | MODIFIER | c.1222-611dupT | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 9/17 | INFO_REALIGN_3_PRIME | chr3 | 158660248 | |||||
chr3:158660367
|
C | T | 141 | a0001c0001t0003g0009a0001c0001t0003g0012a0001c0001t0003g0026others(138): Show | 159 | HG00280.hp2 HG00323.hp1 HG00423.hp1 others(156): Show |
intron_variant | MODIFIER | c.1222-507C>T | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 9/17 | chr3 | 158660367 | ||||||
chr3:158660420
|
G | C | 5 | a0001c0001t0002g0040a0001c0001t0002g0051a0001c0001t0002g0075others(2): Show | 5 | NA18949.hp1 NA18968.hp2 NA18982.hp1 others(2): Show |
intron_variant | MODIFIER | c.1222-454G>C | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 9/17 | chr3 | 158660420 | ||||||
chr3:158660463
|
G | A | 1 | a0001c0004t0024g0283 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.1222-411G>A | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 9/17 | chr3 | 158660463 | ||||||
chr3:158660494
|
C | T | 56 | a0001c0001t0002g0001a0001c0001t0002g0005a0001c0001t0002g0015others(53): Show | 69 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(66): Show |
intron_variant | MODIFIER | c.1222-380C>T | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 9/17 | chr3 | 158660494 | ||||||
chr3:158660495
|
G | A | 51 | a0001c0001t0003g0009a0001c0001t0003g0012a0001c0001t0003g0026others(48): Show | 57 | HG00280.hp2 HG00423.hp1 HG00609.hp2 others(54): Show |
intron_variant | MODIFIER | c.1222-379G>A | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 9/17 | chr3 | 158660495 | ||||||
chr3:158660539
|
T | C | 1 | a0001c0001t0003g0191 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1222-335T>C | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 9/17 | chr3 | 158660539 | ||||||
chr3:158660544
|
C | T | 1 | a0001c0001t0004g0260 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.1222-330C>T | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 9/17 | chr3 | 158660544 | ||||||
chr3:158660553
|
A | G | 2 | a0001c0001t0017g0028a0001c0001t0030g0224 | 3 | HG02895.hp1 HG03130.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.1222-321A>G | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 9/17 | chr3 | 158660553 | ||||||
chr3:158660615
|
G | C | 4 | a0001c0001t0014g0178a0001c0001t0014g0179a0001c0001t0014g0296others(1): Show | 4 | HG03098.hp2 HG03195.hp2 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.1222-259G>C | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 9/17 | chr3 | 158660615 | ||||||
chr3:158660738
|
C | G | 1 | a0001c0001t0018g0304 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.1222-136C>G | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 9/17 | chr3 | 158660738 | ||||||
chr3:158660871
|
T | G | 1 | a0002c0002t0001g0158 | 1 | HG02300.hp1 | splice_region_variant&intron_variant | LOW | c.1222-3T>G | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 9/17 | chr3 | 158660871 | ||||||
chr3:158661047
|
A | G | 28 | a0001c0001t0004g0002a0001c0001t0004g0013a0001c0001t0004g0014others(25): Show | 38 | HG00323.hp1 HG00597.hp2 HG00642.hp2 others(35): Show |
intron_variant | MODIFIER | c.1323+72A>G | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 10/17 | chr3 | 158661047 | ||||||
chr3:158661058
|
A | G | 60 | a0001c0001t0002g0001a0001c0001t0002g0005a0001c0001t0002g0015others(57): Show | 73 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(70): Show |
intron_variant | MODIFIER | c.1323+83A>G | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 10/17 | chr3 | 158661058 | ||||||
chr3:158661299
|
T | A | 1 | a0002c0002t0001g0118 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.1323+324T>A | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 10/17 | chr3 | 158661299 | ||||||
chr3:158661383
|
G | C | 27 | a0001c0001t0004g0002a0001c0001t0004g0013a0001c0001t0004g0014others(24): Show | 37 | HG00323.hp1 HG00597.hp2 HG00642.hp2 others(34): Show |
intron_variant | MODIFIER | c.1323+408G>C | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 10/17 | chr3 | 158661383 | ||||||
chr3:158661439
|
A | G | 4 | a0001c0001t0002g0079a0001c0001t0002g0080a0001c0001t0002g0081others(1): Show | 4 | HG02486.hp2 HG02965.hp1 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.1323+464A>G | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 10/17 | chr3 | 158661439 | ||||||
chr3:158661612
|
C | T | 141 | a0001c0001t0003g0009a0001c0001t0003g0012a0001c0001t0003g0026others(138): Show | 159 | HG00280.hp2 HG00323.hp1 HG00423.hp1 others(156): Show |
intron_variant | MODIFIER | c.1323+637C>T | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 10/17 | chr3 | 158661612 | ||||||
chr3:158661707
|
A | G | 1 | a0002c0002t0001g0116 | 1 | NA18987.hp2 | intron_variant | MODIFIER | c.1323+732A>G | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 10/17 | chr3 | 158661707 | ||||||
chr3:158661742
|
T | C | 1 | a0001c0004t0024g0283 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.1323+767T>C | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 10/17 | chr3 | 158661742 | ||||||
chr3:158661764
|
A | G | 2 | a0001c0001t0004g0225a0001c0001t0004g0226 | 2 | HG03041.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.1323+789A>G | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 10/17 | chr3 | 158661764 | ||||||
chr3:158661860
|
G | A | 141 | a0001c0001t0003g0009a0001c0001t0003g0012a0001c0001t0003g0026others(138): Show | 159 | HG00280.hp2 HG00323.hp1 HG00423.hp1 others(156): Show |
intron_variant | MODIFIER | c.1324-768G>A | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 10/17 | chr3 | 158661860 | ||||||
chr3:158661874
|
G | A | 1 | a0002c0002t0001g0133 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.1324-754G>A | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 10/17 | chr3 | 158661874 | ||||||
chr3:158662156
|
G | A | 3 | a0002c0002t0001g0120a0002c0002t0001g0128a0002c0013t0001g0101 | 3 | NA18947.hp1 NA18957.hp2 NA19000.hp1 |
intron_variant | MODIFIER | c.1324-472G>A | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 10/17 | chr3 | 158662156 | ||||||
chr3:158662164
|
G | C | 1 | a0001c0004t0024g0283 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.1324-464G>C | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 10/17 | chr3 | 158662164 | ||||||
chr3:158662361
|
G | A | 141 | a0001c0001t0003g0009a0001c0001t0003g0012a0001c0001t0003g0026others(138): Show | 159 | HG00280.hp2 HG00323.hp1 HG00423.hp1 others(156): Show |
intron_variant | MODIFIER | c.1324-267G>A | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 10/17 | chr3 | 158662361 | ||||||
chr3:158662438
|
T | C | 1 | a0002c0002t0001g0092 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.1324-190T>C | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 10/17 | chr3 | 158662438 | ||||||
chr3:158662833
|
T | C | 1 | a0002c0002t0001g0152 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.1380+149T>C | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 11/17 | chr3 | 158662833 | ||||||
chr3:158662905
|
T | A | 9 | a0001c0001t0005g0277a0001c0001t0005g0278a0001c0001t0005g0279others(6): Show | 9 | HG01891.hp1 HG02109.hp1 HG02145.hp2 others(6): Show |
intron_variant | MODIFIER | c.1380+221T>A | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 11/17 | chr3 | 158662905 | ||||||
chr3:158662996
|
C | A | 1 | a0001c0004t0024g0283 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.1380+312C>A | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 11/17 | chr3 | 158662996 | ||||||
chr3:158663288
|
A | G | 1 | a0001c0001t0002g0075 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.1380+604A>G | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 11/17 | chr3 | 158663288 | ||||||
chr3:158663301
|
A | C | 1 | a0002c0002t0001g0177 | 1 | NA18951.hp1 | intron_variant | MODIFIER | c.1380+617A>C | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 11/17 | chr3 | 158663301 | ||||||
chr3:158663458
|
A | G | 1 | a0002c0002t0001g0149 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.1380+774A>G | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 11/17 | chr3 | 158663458 | ||||||
chr3:158663511
|
TC | T | 141 | a0001c0001t0003g0009a0001c0001t0003g0012a0001c0001t0003g0026others(138): Show | 159 | HG00280.hp2 HG00323.hp1 HG00423.hp1 others(156): Show |
intron_variant | MODIFIER | c.1380+829delC | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 11/17 | INFO_REALIGN_3_PRIME | chr3 | 158663511 | |||||
chr3:158663598
|
G | C | 3 | a0001c0001t0014g0178a0001c0001t0014g0179a0001c0001t0014g0296 | 3 | HG03098.hp2 HG03486.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.1380+914G>C | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 11/17 | chr3 | 158663598 | ||||||
chr3:158663789
|
A | G | 4 | a0001c0001t0011g0227a0001c0001t0011g0228a0001c0001t0011g0229others(1): Show | 4 | HG01891.hp2 HG02055.hp1 HG02622.hp1 others(1): Show |
intron_variant | MODIFIER | c.1380+1105A>G | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 11/17 | chr3 | 158663789 | ||||||
chr3:158664045
|
A | G | 141 | a0001c0001t0003g0009a0001c0001t0003g0012a0001c0001t0003g0026others(138): Show | 159 | HG00280.hp2 HG00323.hp1 HG00423.hp1 others(156): Show |
intron_variant | MODIFIER | c.1381-1292A>G | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 11/17 | chr3 | 158664045 | ||||||
chr3:158664304
|
G | A | 202 | a0001c0001t0002g0001a0001c0001t0002g0005a0001c0001t0002g0015others(199): Show | 233 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(230): Show |
intron_variant | MODIFIER | c.1381-1033G>A | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 11/17 | chr3 | 158664304 | ||||||
chr3:158664440
|
T | C | 141 | a0001c0001t0003g0009a0001c0001t0003g0012a0001c0001t0003g0026others(138): Show | 159 | HG00280.hp2 HG00323.hp1 HG00423.hp1 others(156): Show |
intron_variant | MODIFIER | c.1381-897T>C | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 11/17 | chr3 | 158664440 | ||||||
chr3:158664523
|
C | A | 2 | a0001c0001t0017g0028a0001c0001t0030g0224 | 3 | HG02895.hp1 HG03130.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.1381-814C>A | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 11/17 | chr3 | 158664523 | ||||||
chr3:158664603
|
A | T | 1 | a0001c0001t0003g0188 | 1 | HG01257.hp2 | intron_variant | MODIFIER | c.1381-734A>T | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 11/17 | chr3 | 158664603 | ||||||
chr3:158664733
|
G | A | 141 | a0001c0001t0003g0009a0001c0001t0003g0012a0001c0001t0003g0026others(138): Show | 159 | HG00280.hp2 HG00323.hp1 HG00423.hp1 others(156): Show |
intron_variant | MODIFIER | c.1381-604G>A | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 11/17 | chr3 | 158664733 | ||||||
chr3:158664760
|
T | C | 1 | a0001c0009t0029g0295 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.1381-577T>C | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 11/17 | chr3 | 158664760 | ||||||
chr3:158664831
|
A | G | 58 | a0001c0001t0004g0002a0001c0001t0004g0013a0001c0001t0004g0014others(55): Show | 69 | HG00323.hp1 HG00597.hp2 HG00642.hp2 others(66): Show |
intron_variant | MODIFIER | c.1381-506A>G | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 11/17 | chr3 | 158664831 | ||||||
chr3:158664929
|
A | G | 7 | a0001c0001t0004g0029a0001c0001t0004g0233a0001c0001t0004g0244others(4): Show | 8 | HG02257.hp1 HG02258.hp1 HG02630.hp1 others(5): Show |
intron_variant | MODIFIER | c.1381-408A>G | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 11/17 | chr3 | 158664929 | ||||||
chr3:158665054
|
G | T | 1 | a0001c0001t0002g0062 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.1381-283G>T | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 11/17 | chr3 | 158665054 | ||||||
chr3:158665060
|
A | G | 3 | a0001c0004t0024g0283a0001c0004t0025g0300a0001c0004t0026g0305 | 3 | HG01243.hp1 HG02647.hp2 NA18947.hp2 |
intron_variant | MODIFIER | c.1381-277A>G | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 11/17 | chr3 | 158665060 | ||||||
chr3:158665100
|
G | A | 1 | a0001c0001t0009g0290 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.1381-237G>A | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 11/17 | chr3 | 158665100 | ||||||
chr3:158665298
|
C | T | 1 | a0003c0003t0007g0235 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.1381-39C>T | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 11/17 | chr3 | 158665298 | ||||||
chr3:158665734
|
A | G | 1 | a0001c0001t0002g0035 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.1518+260A>G | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 12/17 | chr3 | 158665734 | ||||||
chr3:158665915
|
T | C | 58 | a0001c0001t0004g0002a0001c0001t0004g0013a0001c0001t0004g0014others(55): Show | 69 | HG00323.hp1 HG00597.hp2 HG00642.hp2 others(66): Show |
intron_variant | MODIFIER | c.1519-389T>C | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 12/17 | chr3 | 158665915 | ||||||
chr3:158665935
|
A | G | 1 | a0002c0002t0001g0115 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.1519-369A>G | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 12/17 | chr3 | 158665935 | ||||||
chr3:158666093
|
T | C | 139 | a0001c0001t0003g0009a0001c0001t0003g0012a0001c0001t0003g0026others(136): Show | 157 | HG00280.hp2 HG00323.hp1 HG00423.hp1 others(154): Show |
intron_variant | MODIFIER | c.1519-211T>C | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 12/17 | chr3 | 158666093 | ||||||
chr3:158666093
|
T | G | 2 | a0001c0004t0025g0300a0001c0004t0026g0305 | 2 | HG01243.hp1 HG02647.hp2 |
intron_variant | MODIFIER | c.1519-211T>G | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 12/17 | chr3 | 158666093 | ||||||
chr3:158666271
|
A | T | 2 | a0001c0004t0025g0300a0001c0004t0026g0305 | 2 | HG01243.hp1 HG02647.hp2 |
intron_variant | MODIFIER | c.1519-33A>T | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 12/17 | chr3 | 158666271 | ||||||
chr3:158666279
|
A | G | 51 | a0001c0001t0003g0009a0001c0001t0003g0012a0001c0001t0003g0026others(48): Show | 57 | HG00280.hp2 HG00423.hp1 HG00609.hp2 others(54): Show |
intron_variant | MODIFIER | c.1519-25A>G | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 12/17 | chr3 | 158666279 | ||||||
chr3:158666395
|
G | C | 4 | a0001c0001t0011g0227a0001c0001t0011g0228a0001c0001t0011g0229others(1): Show | 4 | HG01891.hp2 HG02055.hp1 HG02622.hp1 others(1): Show |
intron_variant | MODIFIER | c.1601+9G>C | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 13/17 | chr3 | 158666395 | ||||||
chr3:158666424
|
A | G | 7 | a0001c0001t0002g0005a0001c0001t0002g0015a0001c0001t0002g0039others(4): Show | 11 | HG02074.hp1 NA18747.hp2 NA18943.hp2 others(8): Show |
intron_variant | MODIFIER | c.1601+38A>G | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 13/17 | chr3 | 158666424 | ||||||
chr3:158666476
|
T | G | 2 | a0001c0004t0025g0300a0001c0004t0026g0305 | 2 | HG01243.hp1 HG02647.hp2 |
intron_variant | MODIFIER | c.1601+90T>G | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 13/17 | chr3 | 158666476 | ||||||
chr3:158666573
|
A | G | 1 | a0002c0002t0019g0114 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.1601+187A>G | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 13/17 | chr3 | 158666573 | ||||||
chr3:158666674
|
C | T | 2 | a0001c0001t0004g0243a0001c0001t0004g0274 | 2 | HG01516.hp1 HG01517.hp1 |
intron_variant | MODIFIER | c.1601+288C>T | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 13/17 | chr3 | 158666674 | ||||||
chr3:158666944
|
C | A | 60 | a0001c0001t0004g0002a0001c0001t0004g0013a0001c0001t0004g0014others(57): Show | 71 | HG00323.hp1 HG00597.hp2 HG00642.hp2 others(68): Show |
intron_variant | MODIFIER | c.1601+558C>A | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 13/17 | chr3 | 158666944 | ||||||
chr3:158667094
|
C | A | 60 | a0001c0001t0002g0001a0001c0001t0002g0005a0001c0001t0002g0015others(57): Show | 73 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(70): Show |
intron_variant | MODIFIER | c.1601+708C>A | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 13/17 | chr3 | 158667094 | ||||||
chr3:158667097
|
G | A | 1 | a0001c0001t0023g0306 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.1601+711G>A | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 13/17 | chr3 | 158667097 | ||||||
chr3:158667131
|
C | T | 141 | a0001c0001t0003g0009a0001c0001t0003g0012a0001c0001t0003g0026others(138): Show | 159 | HG00280.hp2 HG00323.hp1 HG00423.hp1 others(156): Show |
intron_variant | MODIFIER | c.1601+745C>T | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 13/17 | chr3 | 158667131 | ||||||
chr3:158667617
|
C | A | 1 | a0001c0001t0002g0052 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.1601+1231C>A | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 13/17 | chr3 | 158667617 | ||||||
chr3:158667757
|
C | T | 1 | a0001c0009t0029g0295 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.1601+1371C>T | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 13/17 | chr3 | 158667757 | ||||||
chr3:158667926
|
T | C | 1 | a0001c0004t0024g0283 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.1601+1540T>C | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 13/17 | chr3 | 158667926 | ||||||
chr3:158668007
|
G | C | 26 | a0001c0001t0004g0002a0001c0001t0004g0013a0001c0001t0004g0014others(23): Show | 36 | HG00323.hp1 HG00597.hp2 HG00642.hp2 others(33): Show |
intron_variant | MODIFIER | c.1601+1621G>C | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 13/17 | chr3 | 158668007 | ||||||
chr3:158668086
|
A | G | 1 | a0002c0002t0001g0127 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.1601+1700A>G | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 13/17 | chr3 | 158668086 | ||||||
chr3:158668136
|
C | T | 2 | a0001c0001t0002g0061a0001c0001t0002g0072 | 2 | HG00558.hp2 HG02132.hp1 |
intron_variant | MODIFIER | c.1601+1750C>T | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 13/17 | chr3 | 158668136 | ||||||
chr3:158668177
|
G | C | 239 | a0001c0001t0002g0001a0001c0001t0002g0005a0001c0001t0002g0015others(236): Show | 281 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(278): Show |
intron_variant | MODIFIER | c.1601+1791G>C | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 13/17 | chr3 | 158668177 | ||||||
chr3:158668249
|
C | A | 1 | a0001c0001t0003g0220 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.1601+1863C>A | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 13/17 | chr3 | 158668249 | ||||||
chr3:158668345
|
A | G | 1 | a0002c0002t0001g0110 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.1601+1959A>G | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 13/17 | chr3 | 158668345 | ||||||
chr3:158668438
|
T | C | 2 | a0001c0001t0003g0192a0001c0001t0003g0223 | 2 | HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.1601+2052T>C | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 13/17 | chr3 | 158668438 | ||||||
chr3:158668718
|
A | G | 141 | a0001c0001t0003g0009a0001c0001t0003g0012a0001c0001t0003g0026others(138): Show | 159 | HG00280.hp2 HG00323.hp1 HG00423.hp1 others(156): Show |
intron_variant | MODIFIER | c.1601+2332A>G | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 13/17 | chr3 | 158668718 | ||||||
chr3:158668750
|
G | A | 3 | a0001c0001t0002g0079a0001c0001t0002g0081a0007c0010t0002g0090 | 3 | HG02965.hp1 HG03453.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.1601+2364G>A | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 13/17 | chr3 | 158668750 | ||||||
chr3:158668800
|
A | G | 9 | a0002c0002t0001g0004a0002c0002t0001g0092a0002c0002t0001g0096others(6): Show | 13 | HG00639.hp2 HG00642.hp1 HG00735.hp1 others(10): Show |
intron_variant | MODIFIER | c.1601+2414A>G | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 13/17 | chr3 | 158668800 | ||||||
chr3:158668908
|
A | G | 15 | a0001c0001t0005g0277a0001c0001t0005g0278a0001c0001t0005g0279others(12): Show | 16 | HG01891.hp1 HG01891.hp2 HG02055.hp1 others(13): Show |
intron_variant | MODIFIER | c.1601+2522A>G | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 13/17 | chr3 | 158668908 | ||||||
chr3:158668944
|
C | T | 1 | a0001c0001t0004g0234 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1601+2558C>T | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 13/17 | chr3 | 158668944 | ||||||
chr3:158668948
|
C | T | 141 | a0001c0001t0003g0009a0001c0001t0003g0012a0001c0001t0003g0026others(138): Show | 159 | HG00280.hp2 HG00323.hp1 HG00423.hp1 others(156): Show |
intron_variant | MODIFIER | c.1601+2562C>T | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 13/17 | chr3 | 158668948 | ||||||
chr3:158669002
|
C | T | 1 | a0001c0001t0023g0306 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.1601+2616C>T | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 13/17 | chr3 | 158669002 | ||||||
chr3:158669097
|
C | T | 2 | a0001c0004t0025g0300a0001c0004t0026g0305 | 2 | HG01243.hp1 HG02647.hp2 |
intron_variant | MODIFIER | c.1601+2711C>T | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 13/17 | chr3 | 158669097 | ||||||
chr3:158669102
|
G | A | 15 | a0001c0001t0005g0277a0001c0001t0005g0278a0001c0001t0005g0279others(12): Show | 16 | HG01891.hp1 HG01891.hp2 HG02055.hp1 others(13): Show |
intron_variant | MODIFIER | c.1601+2716G>A | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 13/17 | chr3 | 158669102 | ||||||
chr3:158669698
|
T | C | 141 | a0001c0001t0003g0009a0001c0001t0003g0012a0001c0001t0003g0026others(138): Show | 159 | HG00280.hp2 HG00323.hp1 HG00423.hp1 others(156): Show |
intron_variant | MODIFIER | c.1601+3312T>C | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 13/17 | chr3 | 158669698 | ||||||
chr3:158670050
|
T | G | 1 | a0001c0001t0004g0238 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.1601+3664T>G | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 13/17 | chr3 | 158670050 | ||||||
chr3:158670308
|
C | T | 1 | a0001c0001t0002g0060 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.1601+3922C>T | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 13/17 | chr3 | 158670308 | ||||||
chr3:158670372
|
C | T | 1 | a0001c0001t0003g0189 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.1601+3986C>T | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 13/17 | chr3 | 158670372 | ||||||
chr3:158670439
|
GC | G | 15 | a0001c0001t0005g0277a0001c0001t0005g0278a0001c0001t0005g0279others(12): Show | 16 | HG01891.hp1 HG01891.hp2 HG02055.hp1 others(13): Show |
intron_variant | MODIFIER | c.1601+4056delC | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 13/17 | INFO_REALIGN_3_PRIME | chr3 | 158670439 | |||||
chr3:158670605
|
T | G | 141 | a0001c0001t0003g0009a0001c0001t0003g0012a0001c0001t0003g0026others(138): Show | 159 | HG00280.hp2 HG00323.hp1 HG00423.hp1 others(156): Show |
intron_variant | MODIFIER | c.1601+4219T>G | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 13/17 | chr3 | 158670605 | ||||||
chr3:158670837
|
G | A | 1 | a0002c0002t0001g0086 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.1601+4451G>A | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 13/17 | chr3 | 158670837 | ||||||
chr3:158670917
|
A | G | 1 | a0001c0001t0023g0306 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.1601+4531A>G | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 13/17 | chr3 | 158670917 | ||||||
chr3:158670932
|
C | CAAAGAAA | 141 | a0001c0001t0003g0009a0001c0001t0003g0012a0001c0001t0003g0026others(138): Show | 159 | HG00280.hp2 HG00323.hp1 HG00423.hp1 others(156): Show |
intron_variant | MODIFIER | c.1601+4554_1601+456 others(11): Show |
GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 13/17 | INFO_REALIGN_3_PRIME | chr3 | 158670932 | |||||
chr3:158670991
|
T | C | 201 | a0001c0001t0002g0001a0001c0001t0002g0005a0001c0001t0002g0015others(198): Show | 232 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(229): Show |
intron_variant | MODIFIER | c.1601+4605T>C | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 13/17 | chr3 | 158670991 | ||||||
chr3:158671006
|
C | T | 1 | a0001c0001t0002g0042 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.1601+4620C>T | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 13/17 | chr3 | 158671006 | ||||||
chr3:158671055
|
A | G | 7 | a0001c0001t0003g0206a0001c0001t0003g0210a0001c0001t0003g0212others(4): Show | 7 | HG00423.hp1 NA18954.hp1 NA18956.hp1 others(4): Show |
intron_variant | MODIFIER | c.1601+4669A>G | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 13/17 | chr3 | 158671055 | ||||||
chr3:158671174
|
A | C | 2 | a0001c0001t0004g0225a0001c0001t0004g0226 | 2 | HG03041.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.1601+4788A>C | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 13/17 | chr3 | 158671174 | ||||||
chr3:158671339
|
G | A | 60 | a0001c0001t0004g0002a0001c0001t0004g0013a0001c0001t0004g0014others(57): Show | 71 | HG00323.hp1 HG00597.hp2 HG00642.hp2 others(68): Show |
intron_variant | MODIFIER | c.1601+4953G>A | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 13/17 | chr3 | 158671339 | ||||||
chr3:158671601
|
A | G | 1 | a0002c0002t0001g0085 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.1601+5215A>G | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 13/17 | chr3 | 158671601 | ||||||
chr3:158671601
|
A | T | 1 | a0001c0001t0004g0242 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.1601+5215A>T | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 13/17 | chr3 | 158671601 | ||||||
chr3:158671864
|
C | G | 9 | a0001c0001t0005g0277a0001c0001t0005g0278a0001c0001t0005g0279others(6): Show | 9 | HG01891.hp1 HG02109.hp1 HG02145.hp2 others(6): Show |
intron_variant | MODIFIER | c.1601+5478C>G | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 13/17 | chr3 | 158671864 | ||||||
chr3:158671983
|
C | T | 141 | a0001c0001t0003g0009a0001c0001t0003g0012a0001c0001t0003g0026others(138): Show | 159 | HG00280.hp2 HG00323.hp1 HG00423.hp1 others(156): Show |
intron_variant | MODIFIER | c.1601+5597C>T | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 13/17 | chr3 | 158671983 | ||||||
chr3:158672071
|
C | T | 51 | a0001c0001t0003g0009a0001c0001t0003g0012a0001c0001t0003g0026others(48): Show | 57 | HG00280.hp2 HG00423.hp1 HG00609.hp2 others(54): Show |
intron_variant | MODIFIER | c.1601+5685C>T | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 13/17 | chr3 | 158672071 | ||||||
chr3:158672084
|
T | C | 1 | a0001c0004t0024g0283 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.1601+5698T>C | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 13/17 | chr3 | 158672084 | ||||||
chr3:158672347
|
C | T | 1 | a0002c0002t0001g0093 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.1601+5961C>T | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 13/17 | chr3 | 158672347 | ||||||
chr3:158672433
|
C | T | 1 | a0001c0001t0004g0241 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.1601+6047C>T | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 13/17 | chr3 | 158672433 | ||||||
chr3:158672441
|
G | A | 2 | a0001c0001t0016g0036a0001c0001t0016g0048 | 2 | NA18906.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.1601+6055G>A | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 13/17 | chr3 | 158672441 | ||||||
chr3:158672445
|
T | G | 1 | a0001c0001t0005g0277 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.1601+6059T>G | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 13/17 | chr3 | 158672445 | ||||||
chr3:158672606
|
A | T | 141 | a0001c0001t0003g0009a0001c0001t0003g0012a0001c0001t0003g0026others(138): Show | 159 | HG00280.hp2 HG00323.hp1 HG00423.hp1 others(156): Show |
intron_variant | MODIFIER | c.1601+6220A>T | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 13/17 | chr3 | 158672606 | ||||||
chr3:158672706
|
C | T | 2 | a0001c0001t0003g0192a0001c0001t0003g0223 | 2 | HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.1601+6320C>T | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 13/17 | chr3 | 158672706 | ||||||
chr3:158672745
|
G | C | 2 | a0001c0001t0002g0061a0001c0001t0002g0072 | 2 | HG00558.hp2 HG02132.hp1 |
intron_variant | MODIFIER | c.1601+6359G>C | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 13/17 | chr3 | 158672745 | ||||||
chr3:158672761
|
A | T | 2 | a0001c0004t0025g0300a0001c0004t0026g0305 | 2 | HG01243.hp1 HG02647.hp2 |
intron_variant | MODIFIER | c.1601+6375A>T | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 13/17 | chr3 | 158672761 | ||||||
chr3:158673037
|
C | T | 1 | a0001c0001t0004g0272 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.1601+6651C>T | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 13/17 | chr3 | 158673037 | ||||||
chr3:158673046
|
C | G | 1 | a0001c0001t0005g0281 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.1601+6660C>G | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 13/17 | chr3 | 158673046 | ||||||
chr3:158673169
|
T | C | 6 | a0001c0001t0004g0234a0001c0001t0004g0245a0001c0001t0004g0246others(3): Show | 6 | HG01243.hp2 HG02280.hp1 HG02965.hp2 others(3): Show |
intron_variant | MODIFIER | c.1601+6783T>C | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 13/17 | chr3 | 158673169 | ||||||
chr3:158673195
|
A | G | 13 | a0001c0001t0005g0277a0001c0001t0005g0278a0001c0001t0005g0279others(10): Show | 13 | HG01891.hp1 HG01891.hp2 HG02055.hp1 others(10): Show |
intron_variant | MODIFIER | c.1601+6809A>G | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 13/17 | chr3 | 158673195 | ||||||
chr3:158673306
|
A | G | 5 | a0001c0001t0002g0040a0001c0001t0002g0051a0001c0001t0002g0075others(2): Show | 5 | NA18949.hp1 NA18968.hp2 NA18982.hp1 others(2): Show |
intron_variant | MODIFIER | c.1601+6920A>G | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 13/17 | chr3 | 158673306 | ||||||
chr3:158673332
|
A | C | 1 | a0002c0002t0001g0123 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.1601+6946A>C | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 13/17 | chr3 | 158673332 | ||||||
chr3:158673335
|
C | G | 141 | a0001c0001t0003g0009a0001c0001t0003g0012a0001c0001t0003g0026others(138): Show | 159 | HG00280.hp2 HG00323.hp1 HG00423.hp1 others(156): Show |
intron_variant | MODIFIER | c.1601+6949C>G | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 13/17 | chr3 | 158673335 | ||||||
chr3:158673349
|
G | T | 141 | a0001c0001t0003g0009a0001c0001t0003g0012a0001c0001t0003g0026others(138): Show | 159 | HG00280.hp2 HG00323.hp1 HG00423.hp1 others(156): Show |
intron_variant | MODIFIER | c.1601+6963G>T | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 13/17 | chr3 | 158673349 | ||||||
chr3:158673364
|
A | G | 2 | a0002c0002t0001g0105a0002c0002t0001g0129 | 2 | HG02896.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.1601+6978A>G | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 13/17 | chr3 | 158673364 | ||||||
chr3:158673508
|
C | CT | 7 | a0001c0001t0023g0306a0001c0004t0025g0300a0001c0004t0026g0305others(4): Show | 7 | HG01243.hp1 HG02647.hp2 HG02717.hp1 others(4): Show |
intron_variant | MODIFIER | c.1601+7142dupT | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 13/17 | INFO_REALIGN_3_PRIME | chr3 | 158673508 | |||||
chr3:158673508
|
C | CTTT | 71 | a0001c0001t0003g0009a0001c0001t0003g0012a0001c0001t0003g0026others(68): Show | 77 | HG00280.hp2 HG00423.hp1 HG00609.hp2 others(74): Show |
intron_variant | MODIFIER | c.1601+7140_1601+714 others(7): Show |
GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 13/17 | INFO_REALIGN_3_PRIME | chr3 | 158673508 | |||||
chr3:158673511
|
T | TTC | 59 | a0001c0001t0004g0002a0001c0001t0004g0013a0001c0001t0004g0014others(56): Show | 70 | HG00323.hp1 HG00597.hp2 HG00642.hp2 others(67): Show |
intron_variant | MODIFIER | c.1601+7126_1601+712 others(6): Show |
GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 13/17 | INFO_REALIGN_3_PRIME | chr3 | 158673511 | |||||
chr3:158673513
|
T | C | 1 | a0002c0002t0001g0139 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.1601+7127T>C | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 13/17 | chr3 | 158673513 | ||||||
chr3:158673514
|
T | C | 58 | a0001c0001t0002g0001a0001c0001t0002g0005a0001c0001t0002g0015others(55): Show | 71 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(68): Show |
intron_variant | MODIFIER | c.1601+7128T>C | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 13/17 | chr3 | 158673514 | ||||||
chr3:158673515
|
T | C | 1 | a0001c0001t0002g0062 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.1601+7129T>C | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 13/17 | chr3 | 158673515 | ||||||
chr3:158673640
|
T | C | 1 | a0001c0001t0005g0285 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.1601+7254T>C | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 13/17 | chr3 | 158673640 | ||||||
chr3:158673673
|
G | A | 141 | a0001c0001t0003g0009a0001c0001t0003g0012a0001c0001t0003g0026others(138): Show | 159 | HG00280.hp2 HG00323.hp1 HG00423.hp1 others(156): Show |
intron_variant | MODIFIER | c.1601+7287G>A | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 13/17 | chr3 | 158673673 | ||||||
chr3:158673693
|
A | G | 1 | a0001c0009t0029g0295 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.1601+7307A>G | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 13/17 | chr3 | 158673693 | ||||||
chr3:158673712
|
T | G | 4 | a0001c0001t0002g0079a0001c0001t0002g0080a0001c0001t0002g0081others(1): Show | 4 | HG02486.hp2 HG02965.hp1 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.1601+7326T>G | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 13/17 | chr3 | 158673712 | ||||||
chr3:158673725
|
AAC | A | 2 | a0001c0001t0017g0028a0001c0001t0030g0224 | 3 | HG02895.hp1 HG03130.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.1601+7340_1601+734 others(6): Show |
GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 13/17 | chr3 | 158673725 | ||||||
chr3:158673781
|
G | T | 141 | a0001c0001t0003g0009a0001c0001t0003g0012a0001c0001t0003g0026others(138): Show | 159 | HG00280.hp2 HG00323.hp1 HG00423.hp1 others(156): Show |
intron_variant | MODIFIER | c.1601+7395G>T | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 13/17 | chr3 | 158673781 | ||||||
chr3:158673789
|
C | A | 1 | a0001c0001t0004g0272 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.1601+7403C>A | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 13/17 | chr3 | 158673789 | ||||||
chr3:158673830
|
C | G | 1 | a0001c0001t0002g0080 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.1601+7444C>G | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 13/17 | chr3 | 158673830 | ||||||
chr3:158673853
|
A | C | 141 | a0001c0001t0003g0009a0001c0001t0003g0012a0001c0001t0003g0026others(138): Show | 159 | HG00280.hp2 HG00323.hp1 HG00423.hp1 others(156): Show |
intron_variant | MODIFIER | c.1601+7467A>C | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 13/17 | chr3 | 158673853 | ||||||
chr3:158673924
|
A | G | 1 | a0001c0001t0002g0081 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.1601+7538A>G | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 13/17 | chr3 | 158673924 | ||||||
chr3:158673956
|
CT | C | 141 | a0001c0001t0003g0009a0001c0001t0003g0012a0001c0001t0003g0026others(138): Show | 159 | HG00280.hp2 HG00323.hp1 HG00423.hp1 others(156): Show |
intron_variant | MODIFIER | c.1601+7573delT | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 13/17 | INFO_REALIGN_3_PRIME | chr3 | 158673956 | |||||
chr3:158674056
|
G | A | 141 | a0001c0001t0003g0009a0001c0001t0003g0012a0001c0001t0003g0026others(138): Show | 159 | HG00280.hp2 HG00323.hp1 HG00423.hp1 others(156): Show |
intron_variant | MODIFIER | c.1601+7670G>A | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 13/17 | chr3 | 158674056 | ||||||
chr3:158674080
|
C | CT | 9 | a0001c0001t0002g0076a0001c0001t0002g0088a0001c0001t0003g0205others(6): Show | 9 | HG02145.hp1 HG02145.hp2 HG02738.hp1 others(6): Show |
intron_variant | MODIFIER | c.1601+7711dupT | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 13/17 | INFO_REALIGN_3_PRIME | chr3 | 158674080 | |||||
chr3:158674080
|
CT | C | 63 | a0001c0001t0002g0053a0001c0001t0002g0062a0001c0001t0003g0214others(60): Show | 74 | HG00323.hp1 HG00597.hp2 HG00642.hp2 others(71): Show |
intron_variant | MODIFIER | c.1601+7711delT | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 13/17 | INFO_REALIGN_3_PRIME | chr3 | 158674080 | |||||
chr3:158674086
|
T | C | 1 | a0002c0002t0001g0159 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.1601+7700T>C | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 13/17 | chr3 | 158674086 | ||||||
chr3:158674130
|
C | G | 202 | a0001c0001t0002g0001a0001c0001t0002g0005a0001c0001t0002g0015others(199): Show | 233 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(230): Show |
intron_variant | MODIFIER | c.1601+7744C>G | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 13/17 | chr3 | 158674130 | ||||||
chr3:158674167
|
A | G | 310 | a0001c0001t0002g0001a0001c0001t0002g0005a0001c0001t0002g0015others(307): Show | 368 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(365): Show |
intron_variant | MODIFIER | c.1601+7781A>G | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 13/17 | chr3 | 158674167 | ||||||
chr3:158674216
|
G | C | 1 | a0003c0003t0007g0247 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1602-7779G>C | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 13/17 | chr3 | 158674216 | ||||||
chr3:158674425
|
C | T | 2 | a0002c0002t0001g0017a0002c0002t0001g0104 | 3 | HG02717.hp2 HG03041.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.1602-7570C>T | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 13/17 | chr3 | 158674425 | ||||||
chr3:158674437
|
C | T | 52 | a0001c0001t0004g0002a0001c0001t0004g0013a0001c0001t0004g0014others(49): Show | 63 | HG00323.hp1 HG00597.hp2 HG00642.hp2 others(60): Show |
intron_variant | MODIFIER | c.1602-7558C>T | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 13/17 | chr3 | 158674437 | ||||||
chr3:158674489
|
T | C | 60 | a0001c0001t0002g0001a0001c0001t0002g0005a0001c0001t0002g0015others(57): Show | 73 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(70): Show |
intron_variant | MODIFIER | c.1602-7506T>C | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 13/17 | chr3 | 158674489 | ||||||
chr3:158674684
|
C | T | 7 | a0001c0001t0004g0029a0001c0001t0004g0233a0001c0001t0004g0244others(4): Show | 8 | HG02257.hp1 HG02258.hp1 HG02630.hp1 others(5): Show |
intron_variant | MODIFIER | c.1602-7311C>T | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 13/17 | chr3 | 158674684 | ||||||
chr3:158674699
|
A | T | 7 | a0001c0001t0003g0187a0001c0001t0003g0193a0001c0001t0003g0199others(4): Show | 7 | HG01074.hp1 HG01361.hp2 HG02027.hp2 others(4): Show |
intron_variant | MODIFIER | c.1602-7296A>T | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 13/17 | chr3 | 158674699 | ||||||
chr3:158674710
|
C | G | 1 | a0002c0002t0001g0123 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.1602-7285C>G | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 13/17 | chr3 | 158674710 | ||||||
chr3:158674730
|
T | C | 1 | a0001c0001t0003g0189 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.1602-7265T>C | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 13/17 | chr3 | 158674730 | ||||||
chr3:158674738
|
G | A | 1 | a0002c0002t0001g0095 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.1602-7257G>A | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 13/17 | chr3 | 158674738 | ||||||
chr3:158674931
|
A | C | 2 | a0002c0002t0012g0082a0002c0002t0012g0150 | 2 | NA18985.hp2 NA19079.hp2 |
intron_variant | MODIFIER | c.1602-7064A>C | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 13/17 | chr3 | 158674931 | ||||||
chr3:158675011
|
G | A | 141 | a0001c0001t0003g0009a0001c0001t0003g0012a0001c0001t0003g0026others(138): Show | 159 | HG00280.hp2 HG00323.hp1 HG00423.hp1 others(156): Show |
intron_variant | MODIFIER | c.1602-6984G>A | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 13/17 | chr3 | 158675011 | ||||||
chr3:158675014
|
A | C | 311 | a0001c0001t0002g0001a0001c0001t0002g0005a0001c0001t0002g0015others(308): Show | 369 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(366): Show |
intron_variant | MODIFIER | c.1602-6981A>C | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 13/17 | chr3 | 158675014 | ||||||
chr3:158675014
|
A | T | 2 | a0001c0001t0004g0244a0001c0001t0004g0253 | 2 | HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.1602-6981A>T | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 13/17 | chr3 | 158675014 | ||||||
chr3:158675025
|
A | G | 1 | a0001c0001t0009g0293 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1602-6970A>G | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 13/17 | chr3 | 158675025 | ||||||
chr3:158675147
|
C | T | 2 | a0001c0001t0003g0191a0001c0001t0003g0198 | 2 | HG02572.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.1602-6848C>T | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 13/17 | chr3 | 158675147 | ||||||
chr3:158675154
|
G | A | 1 | a0001c0001t0002g0066 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.1602-6841G>A | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 13/17 | chr3 | 158675154 | ||||||
chr3:158675156
|
G | A | 1 | a0002c0002t0001g0095 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.1602-6839G>A | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 13/17 | chr3 | 158675156 | ||||||
chr3:158675157
|
GGCGCCTG others(8): Show |
G | 5 | a0001c0001t0005g0277a0001c0001t0005g0278a0001c0001t0005g0279others(2): Show | 5 | HG01891.hp1 HG02280.hp2 HG02886.hp2 others(2): Show |
intron_variant | MODIFIER | c.1602-6835_1602-682 others(19): Show |
GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 13/17 | INFO_REALIGN_3_PRIME | chr3 | 158675157 | |||||
chr3:158675159
|
C | T | 1 | a0001c0001t0005g0286 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.1602-6836C>T | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 13/17 | chr3 | 158675159 | ||||||
chr3:158675161
|
C | T | 2 | a0001c0004t0025g0300a0001c0004t0026g0305 | 2 | HG01243.hp1 HG02647.hp2 |
intron_variant | MODIFIER | c.1602-6834C>T | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 13/17 | chr3 | 158675161 | ||||||
chr3:158675218
|
G | A | 3 | a0002c0002t0001g0097a0002c0002t0001g0118a0009c0014t0001g0094 | 3 | HG02109.hp2 HG02717.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.1602-6777G>A | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 13/17 | chr3 | 158675218 | ||||||
chr3:158675285
|
C | CA | 18 | a0002c0002t0001g0024a0002c0002t0001g0085a0002c0002t0001g0095others(15): Show | 19 | HG00597.hp1 HG00621.hp1 HG00738.hp1 others(16): Show |
intron_variant | MODIFIER | c.1602-6685dupA | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 13/17 | INFO_REALIGN_3_PRIME | chr3 | 158675285 | |||||
chr3:158675285
|
CA | C | 66 | a0001c0001t0003g0183a0001c0001t0003g0187a0001c0001t0003g0194others(63): Show | 77 | HG00323.hp1 HG00423.hp1 HG00597.hp2 others(74): Show |
intron_variant | MODIFIER | c.1602-6685delA | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 13/17 | INFO_REALIGN_3_PRIME | chr3 | 158675285 | |||||
chr3:158675285
|
CAA | C | 47 | a0001c0001t0003g0009a0001c0001t0003g0012a0001c0001t0003g0026others(44): Show | 53 | HG00280.hp2 HG01069.hp2 HG01074.hp1 others(50): Show |
intron_variant | MODIFIER | c.1602-6686_1602-668 others(6): Show |
GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 13/17 | INFO_REALIGN_3_PRIME | chr3 | 158675285 | |||||
chr3:158675285
|
CAAAAAAA others(5): Show |
C | 1 | a0002c0002t0001g0168 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.1602-6696_1602-668 others(16): Show |
GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 13/17 | INFO_REALIGN_3_PRIME | chr3 | 158675285 | |||||
chr3:158675285
|
CAAAAAAA others(6): Show |
C | 5 | a0001c0001t0005g0277a0001c0001t0005g0278a0001c0001t0005g0279others(2): Show | 5 | HG01891.hp1 HG02280.hp2 HG02886.hp2 others(2): Show |
intron_variant | MODIFIER | c.1602-6697_1602-668 others(17): Show |
GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 13/17 | INFO_REALIGN_3_PRIME | chr3 | 158675285 | |||||
chr3:158675305
|
A | C | 3 | a0002c0002t0001g0083a0002c0002t0001g0145a0002c0002t0001g0146 | 3 | HG03491.hp2 HG03492.hp1 HG04115.hp1 |
intron_variant | MODIFIER | c.1602-6690A>C | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 13/17 | chr3 | 158675305 | ||||||
chr3:158675306
|
A | C | 2 | a0002c0002t0001g0128a0002c0013t0001g0101 | 2 | NA18947.hp1 NA18957.hp2 |
intron_variant | MODIFIER | c.1602-6689A>C | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 13/17 | chr3 | 158675306 | ||||||
chr3:158675309
|
A | AG | 22 | a0001c0001t0002g0035a0001c0001t0002g0044a0001c0001t0002g0047others(19): Show | 22 | HG00423.hp2 HG01109.hp2 HG01175.hp1 others(19): Show |
intron_variant | MODIFIER | c.1602-6686_1602-668 others(5): Show |
GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 13/17 | chr3 | 158675309 | ||||||
chr3:158675309
|
A | G | 179 | a0001c0001t0002g0001a0001c0001t0002g0005a0001c0001t0002g0015others(176): Show | 210 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(207): Show |
intron_variant | MODIFIER | c.1602-6686A>G | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 13/17 | chr3 | 158675309 | ||||||
chr3:158675310
|
A | G | 201 | a0001c0001t0002g0001a0001c0001t0002g0005a0001c0001t0002g0015others(198): Show | 232 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(229): Show |
intron_variant | MODIFIER | c.1602-6685A>G | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 13/17 | chr3 | 158675310 | ||||||
chr3:158675389
|
A | T | 141 | a0001c0001t0003g0009a0001c0001t0003g0012a0001c0001t0003g0026others(138): Show | 159 | HG00280.hp2 HG00323.hp1 HG00423.hp1 others(156): Show |
intron_variant | MODIFIER | c.1602-6606A>T | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 13/17 | chr3 | 158675389 | ||||||
chr3:158675587
|
A | G | 1 | a0001c0004t0024g0283 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.1602-6408A>G | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 13/17 | chr3 | 158675587 | ||||||
chr3:158675631
|
G | A | 1 | a0001c0001t0002g0031 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.1602-6364G>A | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 13/17 | chr3 | 158675631 | ||||||
chr3:158675899
|
A | G | 2 | a0002c0002t0001g0096a0002c0002t0001g0099 | 2 | HG02055.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.1602-6096A>G | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 13/17 | chr3 | 158675899 | ||||||
chr3:158675933
|
T | G | 141 | a0001c0001t0003g0009a0001c0001t0003g0012a0001c0001t0003g0026others(138): Show | 159 | HG00280.hp2 HG00323.hp1 HG00423.hp1 others(156): Show |
intron_variant | MODIFIER | c.1602-6062T>G | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 13/17 | chr3 | 158675933 | ||||||
chr3:158675961
|
T | C | 1 | a0001c0001t0002g0035 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.1602-6034T>C | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 13/17 | chr3 | 158675961 | ||||||
chr3:158676059
|
G | A | 1 | a0005c0006t0011g0298 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.1602-5936G>A | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 13/17 | chr3 | 158676059 | ||||||
chr3:158676150
|
T | G | 12 | a0001c0001t0009g0289a0001c0001t0009g0290a0001c0001t0009g0291others(9): Show | 12 | HG01884.hp1 HG02258.hp2 HG02622.hp2 others(9): Show |
intron_variant | MODIFIER | c.1602-5845T>G | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 13/17 | chr3 | 158676150 | ||||||
chr3:158676220
|
T | G | 13 | a0001c0001t0005g0277a0001c0001t0005g0278a0001c0001t0005g0279others(10): Show | 13 | HG01891.hp1 HG01891.hp2 HG02055.hp1 others(10): Show |
intron_variant | MODIFIER | c.1602-5775T>G | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 13/17 | chr3 | 158676220 | ||||||
chr3:158676224
|
A | G | 202 | a0001c0001t0002g0001a0001c0001t0002g0005a0001c0001t0002g0015others(199): Show | 233 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(230): Show |
intron_variant | MODIFIER | c.1602-5771A>G | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 13/17 | chr3 | 158676224 | ||||||
chr3:158676321
|
T | G | 1 | a0001c0001t0004g0273 | 1 | NA18992.hp1 | intron_variant | MODIFIER | c.1602-5674T>G | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 13/17 | chr3 | 158676321 | ||||||
chr3:158676324
|
G | A | 1 | a0001c0001t0004g0273 | 1 | NA18992.hp1 | intron_variant | MODIFIER | c.1602-5671G>A | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 13/17 | chr3 | 158676324 | ||||||
chr3:158676324
|
G | GA | 140 | a0001c0001t0003g0009a0001c0001t0003g0012a0001c0001t0003g0026others(137): Show | 158 | HG00280.hp2 HG00323.hp1 HG00423.hp1 others(155): Show |
intron_variant | MODIFIER | c.1602-5668dupA | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 13/17 | INFO_REALIGN_3_PRIME | chr3 | 158676324 | |||||
chr3:158676431
|
C | T | 1 | a0001c0001t0014g0296 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.1602-5564C>T | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 13/17 | chr3 | 158676431 | ||||||
chr3:158676701
|
C | CT | 13 | a0001c0001t0003g0197a0001c0001t0005g0277a0001c0001t0005g0278others(10): Show | 13 | HG01891.hp1 HG02109.hp1 HG02145.hp1 others(10): Show |
intron_variant | MODIFIER | c.1602-5279dupT | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 13/17 | INFO_REALIGN_3_PRIME | chr3 | 158676701 | |||||
chr3:158676701
|
CT | C | 60 | a0001c0001t0002g0001a0001c0001t0002g0005a0001c0001t0002g0015others(57): Show | 73 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(70): Show |
intron_variant | MODIFIER | c.1602-5279delT | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 13/17 | INFO_REALIGN_3_PRIME | chr3 | 158676701 | |||||
chr3:158676721
|
CAG | C | 1 | a0001c0001t0003g0012 | 3 | NA18955.hp1 NA19056.hp1 NA19072.hp1 |
intron_variant | MODIFIER | c.1602-5271_1602-527 others(6): Show |
GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 13/17 | INFO_REALIGN_3_PRIME | chr3 | 158676721 | |||||
chr3:158676785
|
C | T | 1 | a0002c0002t0001g0121 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.1602-5210C>T | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 13/17 | chr3 | 158676785 | ||||||
chr3:158676910
|
G | A | 1 | a0001c0001t0023g0306 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.1602-5085G>A | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 13/17 | chr3 | 158676910 | ||||||
chr3:158676935
|
A | T | 1 | a0002c0002t0001g0147 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.1602-5060A>T | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 13/17 | chr3 | 158676935 | ||||||
chr3:158676947
|
G | A | 1 | a0001c0004t0024g0283 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.1602-5048G>A | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 13/17 | chr3 | 158676947 | ||||||
chr3:158676995
|
C | T | 1 | a0001c0004t0024g0283 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.1602-5000C>T | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 13/17 | chr3 | 158676995 | ||||||
chr3:158677008
|
A | G | 13 | a0001c0001t0005g0277a0001c0001t0005g0278a0001c0001t0005g0279others(10): Show | 13 | HG01891.hp1 HG01891.hp2 HG02055.hp1 others(10): Show |
intron_variant | MODIFIER | c.1602-4987A>G | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 13/17 | chr3 | 158677008 | ||||||
chr3:158677095
|
T | C | 1 | a0002c0002t0001g0147 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.1602-4900T>C | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 13/17 | chr3 | 158677095 | ||||||
chr3:158677124
|
T | C | 1 | a0001c0001t0023g0306 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.1602-4871T>C | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 13/17 | chr3 | 158677124 | ||||||
chr3:158677155
|
A | G | 202 | a0001c0001t0002g0001a0001c0001t0002g0005a0001c0001t0002g0015others(199): Show | 233 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(230): Show |
intron_variant | MODIFIER | c.1602-4840A>G | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 13/17 | chr3 | 158677155 | ||||||
chr3:158677262
|
A | C | 1 | a0001c0001t0023g0306 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.1602-4733A>C | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 13/17 | chr3 | 158677262 | ||||||
chr3:158677304
|
G | A | 2 | a0001c0004t0025g0300a0001c0004t0026g0305 | 2 | HG01243.hp1 HG02647.hp2 |
intron_variant | MODIFIER | c.1602-4691G>A | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 13/17 | chr3 | 158677304 | ||||||
chr3:158677416
|
A | G | 9 | a0001c0001t0005g0277a0001c0001t0005g0278a0001c0001t0005g0279others(6): Show | 9 | HG01891.hp1 HG02109.hp1 HG02145.hp2 others(6): Show |
intron_variant | MODIFIER | c.1602-4579A>G | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 13/17 | chr3 | 158677416 | ||||||
chr3:158677540
|
G | A | 2 | a0001c0004t0025g0300a0001c0004t0026g0305 | 2 | HG01243.hp1 HG02647.hp2 |
intron_variant | MODIFIER | c.1602-4455G>A | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 13/17 | chr3 | 158677540 | ||||||
chr3:158677575
|
A | G | 1 | a0001c0001t0004g0256 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.1602-4420A>G | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 13/17 | chr3 | 158677575 | ||||||
chr3:158677662
|
G | A | 9 | a0001c0001t0005g0277a0001c0001t0005g0278a0001c0001t0005g0279others(6): Show | 9 | HG01891.hp1 HG02109.hp1 HG02145.hp2 others(6): Show |
intron_variant | MODIFIER | c.1602-4333G>A | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 13/17 | chr3 | 158677662 | ||||||
chr3:158677669
|
T | C | 2 | a0002c0002t0001g0141a0002c0002t0001g0142 | 2 | NA18946.hp2 NA18966.hp1 |
intron_variant | MODIFIER | c.1602-4326T>C | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 13/17 | chr3 | 158677669 | ||||||
chr3:158677754
|
G | A | 2 | a0001c0004t0025g0300a0001c0004t0026g0305 | 2 | HG01243.hp1 HG02647.hp2 |
intron_variant | MODIFIER | c.1602-4241G>A | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 13/17 | chr3 | 158677754 | ||||||
chr3:158677881
|
G | A | 199 | a0001c0001t0002g0001a0001c0001t0002g0005a0001c0001t0002g0015others(196): Show | 230 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(227): Show |
intron_variant | MODIFIER | c.1602-4114G>A | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 13/17 | chr3 | 158677881 | ||||||
chr3:158677888
|
G | A | 51 | a0001c0001t0003g0009a0001c0001t0003g0012a0001c0001t0003g0026others(48): Show | 57 | HG00280.hp2 HG00423.hp1 HG00609.hp2 others(54): Show |
intron_variant | MODIFIER | c.1602-4107G>A | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 13/17 | chr3 | 158677888 | ||||||
chr3:158677950
|
G | C | 8 | a0001c0001t0007g0255a0003c0003t0007g0230a0003c0003t0007g0235others(5): Show | 8 | HG01175.hp1 HG02257.hp2 HG02486.hp1 others(5): Show |
intron_variant | MODIFIER | c.1602-4045G>C | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 13/17 | chr3 | 158677950 | ||||||
chr3:158678077
|
G | C | 60 | a0001c0001t0002g0001a0001c0001t0002g0005a0001c0001t0002g0015others(57): Show | 73 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(70): Show |
intron_variant | MODIFIER | c.1602-3918G>C | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 13/17 | chr3 | 158678077 | ||||||
chr3:158678101
|
T | C | 1 | a0001c0001t0004g0225 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.1602-3894T>C | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 13/17 | chr3 | 158678101 | ||||||
chr3:158678217
|
A | C | 1 | a0001c0001t0003g0197 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.1602-3778A>C | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 13/17 | chr3 | 158678217 | ||||||
chr3:158678297
|
T | C | 1 | a0001c0001t0005g0286 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.1602-3698T>C | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 13/17 | chr3 | 158678297 | ||||||
chr3:158678310
|
G | A | 1 | a0002c0002t0001g0018 | 2 | HG00639.hp1 HG01070.hp2 |
intron_variant | MODIFIER | c.1602-3685G>A | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 13/17 | chr3 | 158678310 | ||||||
chr3:158678389
|
C | T | 1 | a0001c0001t0002g0035 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.1602-3606C>T | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 13/17 | chr3 | 158678389 | ||||||
chr3:158678617
|
A | T | 141 | a0001c0001t0003g0009a0001c0001t0003g0012a0001c0001t0003g0026others(138): Show | 159 | HG00280.hp2 HG00323.hp1 HG00423.hp1 others(156): Show |
intron_variant | MODIFIER | c.1602-3378A>T | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 13/17 | chr3 | 158678617 | ||||||
chr3:158678696
|
T | TAAA | 141 | a0001c0001t0003g0009a0001c0001t0003g0012a0001c0001t0003g0026others(138): Show | 159 | HG00280.hp2 HG00323.hp1 HG00423.hp1 others(156): Show |
intron_variant | MODIFIER | c.1602-3298_1602-329 others(7): Show |
GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 13/17 | INFO_REALIGN_3_PRIME | chr3 | 158678696 | |||||
chr3:158678735
|
G | T | 141 | a0001c0001t0003g0009a0001c0001t0003g0012a0001c0001t0003g0026others(138): Show | 159 | HG00280.hp2 HG00323.hp1 HG00423.hp1 others(156): Show |
intron_variant | MODIFIER | c.1602-3260G>T | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 13/17 | chr3 | 158678735 | ||||||
chr3:158678796
|
C | T | 141 | a0001c0001t0003g0009a0001c0001t0003g0012a0001c0001t0003g0026others(138): Show | 159 | HG00280.hp2 HG00323.hp1 HG00423.hp1 others(156): Show |
intron_variant | MODIFIER | c.1602-3199C>T | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 13/17 | chr3 | 158678796 | ||||||
chr3:158678856
|
A | G | 2 | a0001c0004t0025g0300a0001c0004t0026g0305 | 2 | HG01243.hp1 HG02647.hp2 |
intron_variant | MODIFIER | c.1602-3139A>G | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 13/17 | chr3 | 158678856 | ||||||
chr3:158679047
|
A | T | 8 | a0001c0001t0007g0255a0003c0003t0007g0230a0003c0003t0007g0235others(5): Show | 8 | HG01175.hp1 HG02257.hp2 HG02486.hp1 others(5): Show |
intron_variant | MODIFIER | c.1602-2948A>T | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 13/17 | chr3 | 158679047 | ||||||
chr3:158679052
|
C | T | 12 | a0001c0001t0009g0289a0001c0001t0009g0290a0001c0001t0009g0291others(9): Show | 12 | HG01884.hp1 HG02258.hp2 HG02622.hp2 others(9): Show |
intron_variant | MODIFIER | c.1602-2943C>T | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 13/17 | chr3 | 158679052 | ||||||
chr3:158679058
|
C | T | 1 | a0001c0001t0004g0256 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.1602-2937C>T | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 13/17 | chr3 | 158679058 | ||||||
chr3:158679417
|
G | A | 141 | a0001c0001t0003g0009a0001c0001t0003g0012a0001c0001t0003g0026others(138): Show | 159 | HG00280.hp2 HG00323.hp1 HG00423.hp1 others(156): Show |
intron_variant | MODIFIER | c.1602-2578G>A | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 13/17 | chr3 | 158679417 | ||||||
chr3:158679466
|
T | TA | 3 | a0002c0002t0001g0138a0002c0002t0001g0143a0006c0015t0001g0140 | 3 | HG01109.hp1 HG01123.hp1 HG02602.hp1 |
intron_variant | MODIFIER | c.1602-2528dupA | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 13/17 | INFO_REALIGN_3_PRIME | chr3 | 158679466 | |||||
chr3:158679514
|
A | G | 1 | a0001c0001t0005g0280 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.1602-2481A>G | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 13/17 | chr3 | 158679514 | ||||||
chr3:158679535
|
A | G | 2 | a0002c0002t0001g0136a0002c0002t0001g0169 | 2 | NA19055.hp2 NA19066.hp1 |
intron_variant | MODIFIER | c.1602-2460A>G | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 13/17 | chr3 | 158679535 | ||||||
chr3:158679588
|
C | T | 1 | a0001c0001t0004g0282 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.1602-2407C>T | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 13/17 | chr3 | 158679588 | ||||||
chr3:158679910
|
G | A | 3 | a0001c0004t0024g0283a0001c0004t0025g0300a0001c0004t0026g0305 | 3 | HG01243.hp1 HG02647.hp2 NA18947.hp2 |
intron_variant | MODIFIER | c.1602-2085G>A | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 13/17 | chr3 | 158679910 | ||||||
chr3:158680007
|
C | T | 2 | a0001c0004t0025g0300a0001c0004t0026g0305 | 2 | HG01243.hp1 HG02647.hp2 |
intron_variant | MODIFIER | c.1602-1988C>T | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 13/17 | chr3 | 158680007 | ||||||
chr3:158680053
|
C | T | 60 | a0001c0001t0002g0001a0001c0001t0002g0005a0001c0001t0002g0015others(57): Show | 73 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(70): Show |
intron_variant | MODIFIER | c.1602-1942C>T | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 13/17 | chr3 | 158680053 | ||||||
chr3:158680063
|
G | C | 9 | a0001c0001t0005g0277a0001c0001t0005g0278a0001c0001t0005g0279others(6): Show | 9 | HG01891.hp1 HG02109.hp1 HG02145.hp2 others(6): Show |
intron_variant | MODIFIER | c.1602-1932G>C | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 13/17 | chr3 | 158680063 | ||||||
chr3:158680164
|
A | C | 1 | a0002c0002t0001g0102 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.1602-1831A>C | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 13/17 | chr3 | 158680164 | ||||||
chr3:158680166
|
A | T | 1 | a0002c0002t0001g0166 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.1602-1829A>T | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 13/17 | chr3 | 158680166 | ||||||
chr3:158680195
|
G | C | 1 | a0001c0001t0027g0236 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.1602-1800G>C | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 13/17 | chr3 | 158680195 | ||||||
chr3:158680221
|
G | A | 51 | a0001c0001t0003g0009a0001c0001t0003g0012a0001c0001t0003g0026others(48): Show | 57 | HG00280.hp2 HG00423.hp1 HG00609.hp2 others(54): Show |
intron_variant | MODIFIER | c.1602-1774G>A | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 13/17 | chr3 | 158680221 | ||||||
chr3:158680275
|
AG | A | 9 | a0001c0001t0005g0277a0001c0001t0005g0278a0001c0001t0005g0279others(6): Show | 9 | HG01891.hp1 HG02109.hp1 HG02145.hp2 others(6): Show |
intron_variant | MODIFIER | c.1602-1718delG | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 13/17 | INFO_REALIGN_3_PRIME | chr3 | 158680275 | |||||
chr3:158680432
|
G | C | 141 | a0001c0001t0003g0009a0001c0001t0003g0012a0001c0001t0003g0026others(138): Show | 159 | HG00280.hp2 HG00323.hp1 HG00423.hp1 others(156): Show |
intron_variant | MODIFIER | c.1602-1563G>C | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 13/17 | chr3 | 158680432 | ||||||
chr3:158680491
|
G | T | 141 | a0001c0001t0003g0009a0001c0001t0003g0012a0001c0001t0003g0026others(138): Show | 159 | HG00280.hp2 HG00323.hp1 HG00423.hp1 others(156): Show |
intron_variant | MODIFIER | c.1602-1504G>T | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 13/17 | chr3 | 158680491 | ||||||
chr3:158680492
|
G | C | 141 | a0001c0001t0003g0009a0001c0001t0003g0012a0001c0001t0003g0026others(138): Show | 159 | HG00280.hp2 HG00323.hp1 HG00423.hp1 others(156): Show |
intron_variant | MODIFIER | c.1602-1503G>C | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 13/17 | chr3 | 158680492 | ||||||
chr3:158680531
|
A | T | 141 | a0001c0001t0003g0009a0001c0001t0003g0012a0001c0001t0003g0026others(138): Show | 159 | HG00280.hp2 HG00323.hp1 HG00423.hp1 others(156): Show |
intron_variant | MODIFIER | c.1602-1464A>T | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 13/17 | chr3 | 158680531 | ||||||
chr3:158680779
|
T | C | 1 | a0001c0001t0002g0060 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.1602-1216T>C | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 13/17 | chr3 | 158680779 | ||||||
chr3:158680795
|
C | G | 1 | a0001c0001t0003g0203 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.1602-1200C>G | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 13/17 | chr3 | 158680795 | ||||||
chr3:158680849
|
G | A | 141 | a0001c0001t0003g0009a0001c0001t0003g0012a0001c0001t0003g0026others(138): Show | 159 | HG00280.hp2 HG00323.hp1 HG00423.hp1 others(156): Show |
intron_variant | MODIFIER | c.1602-1146G>A | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 13/17 | chr3 | 158680849 | ||||||
chr3:158680927
|
C | T | 60 | a0001c0001t0002g0001a0001c0001t0002g0005a0001c0001t0002g0015others(57): Show | 73 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(70): Show |
intron_variant | MODIFIER | c.1602-1068C>T | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 13/17 | chr3 | 158680927 | ||||||
chr3:158681482
|
C | A | 1 | a0001c0001t0023g0306 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.1602-513C>A | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 13/17 | chr3 | 158681482 | ||||||
chr3:158681545
|
TAATGCCC others(10): Show |
T | 2 | a0001c0004t0025g0300a0001c0004t0026g0305 | 2 | HG01243.hp1 HG02647.hp2 |
intron_variant | MODIFIER | c.1602-448_1602-432d others(19): Show |
GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 13/17 | INFO_REALIGN_3_PRIME | chr3 | 158681545 | |||||
chr3:158681798
|
C | T | 3 | a0001c0001t0014g0178a0001c0001t0014g0179a0001c0001t0014g0296 | 3 | HG03098.hp2 HG03486.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.1602-197C>T | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 13/17 | chr3 | 158681798 | ||||||
chr3:158681968
|
A | AT | 141 | a0001c0001t0003g0009a0001c0001t0003g0012a0001c0001t0003g0026others(138): Show | 159 | HG00280.hp2 HG00323.hp1 HG00423.hp1 others(156): Show |
intron_variant | MODIFIER | c.1602-17dupT | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 13/17 | INFO_REALIGN_3_PRIME | chr3 | 158681968 | |||||
chr3:158682472
|
A | T | 7 | a0002c0002t0001g0008a0002c0002t0001g0022a0002c0002t0001g0023others(4): Show | 11 | HG00597.hp1 HG02040.hp2 NA18944.hp2 others(8): Show |
intron_variant | MODIFIER | c.1764+315A>T | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 14/17 | chr3 | 158682472 | ||||||
chr3:158682473
|
T | C | 1 | a0001c0001t0003g0193 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.1764+316T>C | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 14/17 | chr3 | 158682473 | ||||||
chr3:158682587
|
T | C | 141 | a0001c0001t0003g0009a0001c0001t0003g0012a0001c0001t0003g0026others(138): Show | 159 | HG00280.hp2 HG00323.hp1 HG00423.hp1 others(156): Show |
intron_variant | MODIFIER | c.1764+430T>C | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 14/17 | chr3 | 158682587 | ||||||
chr3:158682710
|
T | C | 141 | a0001c0001t0003g0009a0001c0001t0003g0012a0001c0001t0003g0026others(138): Show | 159 | HG00280.hp2 HG00323.hp1 HG00423.hp1 others(156): Show |
intron_variant | MODIFIER | c.1764+553T>C | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 14/17 | chr3 | 158682710 | ||||||
chr3:158682747
|
G | A | 141 | a0001c0001t0003g0009a0001c0001t0003g0012a0001c0001t0003g0026others(138): Show | 159 | HG00280.hp2 HG00323.hp1 HG00423.hp1 others(156): Show |
intron_variant | MODIFIER | c.1764+590G>A | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 14/17 | chr3 | 158682747 | ||||||
chr3:158682790
|
C | T | 7 | a0001c0001t0004g0029a0001c0001t0004g0233a0001c0001t0004g0244others(4): Show | 8 | HG02257.hp1 HG02258.hp1 HG02630.hp1 others(5): Show |
intron_variant | MODIFIER | c.1764+633C>T | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 14/17 | chr3 | 158682790 | ||||||
chr3:158683036
|
G | GA | 37 | a0001c0001t0002g0032a0001c0001t0002g0047a0001c0001t0002g0054others(34): Show | 39 | HG00140.hp2 HG00423.hp2 HG00639.hp1 others(36): Show |
intron_variant | MODIFIER | c.1764+896dupA | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 14/17 | INFO_REALIGN_3_PRIME | chr3 | 158683036 | |||||
chr3:158683243
|
A | G | 51 | a0001c0001t0003g0009a0001c0001t0003g0012a0001c0001t0003g0026others(48): Show | 57 | HG00280.hp2 HG00423.hp1 HG00609.hp2 others(54): Show |
intron_variant | MODIFIER | c.1764+1086A>G | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 14/17 | chr3 | 158683243 | ||||||
chr3:158683320
|
T | C | 1 | a0002c0002t0001g0126 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.1764+1163T>C | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 14/17 | chr3 | 158683320 | ||||||
chr3:158683327
|
G | A | 3 | a0001c0001t0014g0178a0001c0001t0014g0179a0001c0001t0014g0296 | 3 | HG03098.hp2 HG03486.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.1764+1170G>A | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 14/17 | chr3 | 158683327 | ||||||
chr3:158683377
|
T | G | 28 | a0001c0001t0004g0002a0001c0001t0004g0013a0001c0001t0004g0014others(25): Show | 38 | HG00323.hp1 HG00597.hp2 HG00642.hp2 others(35): Show |
intron_variant | MODIFIER | c.1765-1147T>G | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 14/17 | chr3 | 158683377 | ||||||
chr3:158683467
|
A | G | 2 | a0002c0002t0001g0086a0002c0002t0001g0087 | 2 | HG02027.hp1 HG03017.hp1 |
intron_variant | MODIFIER | c.1765-1057A>G | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 14/17 | chr3 | 158683467 | ||||||
chr3:158683486
|
A | G | 3 | a0001c0001t0004g0225a0001c0001t0004g0226a0001c0001t0023g0306 | 3 | HG03041.hp1 HG03225.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.1765-1038A>G | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 14/17 | chr3 | 158683486 | ||||||
chr3:158683505
|
A | T | 23 | a0001c0001t0005g0277a0001c0001t0005g0278a0001c0001t0005g0279others(20): Show | 24 | HG01175.hp1 HG01891.hp1 HG01891.hp2 others(21): Show |
intron_variant | MODIFIER | c.1765-1019A>T | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 14/17 | chr3 | 158683505 | ||||||
chr3:158683512
|
A | G | 6 | a0001c0001t0009g0289a0001c0001t0009g0290a0001c0001t0009g0291others(3): Show | 6 | HG01884.hp1 HG02258.hp2 HG02622.hp2 others(3): Show |
intron_variant | MODIFIER | c.1765-1012A>G | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 14/17 | chr3 | 158683512 | ||||||
chr3:158683556
|
G | A | 2 | a0003c0003t0007g0248a0003c0003t0007g0261 | 2 | HG02630.hp2 HG02818.hp2 |
intron_variant | MODIFIER | c.1765-968G>A | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 14/17 | chr3 | 158683556 | ||||||
chr3:158683584
|
T | G | 1 | a0001c0001t0003g0189 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.1765-940T>G | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 14/17 | chr3 | 158683584 | ||||||
chr3:158683765
|
A | T | 51 | a0001c0001t0003g0009a0001c0001t0003g0012a0001c0001t0003g0026others(48): Show | 57 | HG00280.hp2 HG00423.hp1 HG00609.hp2 others(54): Show |
intron_variant | MODIFIER | c.1765-759A>T | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 14/17 | chr3 | 158683765 | ||||||
chr3:158684117
|
C | G | 23 | a0001c0001t0005g0277a0001c0001t0005g0278a0001c0001t0005g0279others(20): Show | 24 | HG01175.hp1 HG01891.hp1 HG01891.hp2 others(21): Show |
intron_variant | MODIFIER | c.1765-407C>G | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 14/17 | chr3 | 158684117 | ||||||
chr3:158684146
|
A | C | 1 | a0001c0001t0023g0306 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.1765-378A>C | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 14/17 | chr3 | 158684146 | ||||||
chr3:158684171
|
G | A | 1 | a0001c0001t0023g0306 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.1765-353G>A | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 14/17 | chr3 | 158684171 | ||||||
chr3:158684184
|
C | T | 1 | a0002c0002t0001g0144 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1765-340C>T | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 14/17 | chr3 | 158684184 | ||||||
chr3:158684226
|
A | G | 51 | a0001c0001t0003g0009a0001c0001t0003g0012a0001c0001t0003g0026others(48): Show | 57 | HG00280.hp2 HG00423.hp1 HG00609.hp2 others(54): Show |
intron_variant | MODIFIER | c.1765-298A>G | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 14/17 | chr3 | 158684226 | ||||||
chr3:158684430
|
C | T | 1 | a0001c0001t0023g0306 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.1765-94C>T | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 14/17 | chr3 | 158684430 | ||||||
chr3:158684491
|
C | T | 1 | a0001c0001t0003g0202 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.1765-33C>T | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 14/17 | chr3 | 158684491 | ||||||
chr3:158684799
|
C | T | 6 | a0001c0001t0008g0262a0001c0001t0008g0267a0001c0001t0008g0269others(3): Show | 6 | HG01884.hp2 HG02647.hp1 HG02886.hp1 others(3): Show |
intron_variant | MODIFIER | c.1909+131C>T | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 15/17 | chr3 | 158684799 | ||||||
chr3:158684900
|
A | C | 3 | a0002c0002t0001g0097a0002c0002t0001g0118a0009c0014t0001g0094 | 3 | HG02109.hp2 HG02717.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.1909+232A>C | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 15/17 | chr3 | 158684900 | ||||||
chr3:158685002
|
C | CTTG | 202 | a0001c0001t0002g0001a0001c0001t0002g0005a0001c0001t0002g0015others(199): Show | 233 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(230): Show |
intron_variant | MODIFIER | c.1909+336_1909+337i others(5): Show |
GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 15/17 | INFO_REALIGN_3_PRIME | chr3 | 158685002 | |||||
chr3:158685016
|
C | G | 1 | a0001c0001t0004g0282 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.1909+348C>G | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 15/17 | chr3 | 158685016 | ||||||
chr3:158685252
|
G | T | 1 | a0001c0004t0025g0300 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.1909+584G>T | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 15/17 | chr3 | 158685252 | ||||||
chr3:158685405
|
C | T | 1 | a0002c0002t0001g0124 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.1909+737C>T | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 15/17 | chr3 | 158685405 | ||||||
chr3:158685529
|
G | A | 51 | a0001c0001t0003g0009a0001c0001t0003g0012a0001c0001t0003g0026others(48): Show | 57 | HG00280.hp2 HG00423.hp1 HG00609.hp2 others(54): Show |
intron_variant | MODIFIER | c.1909+861G>A | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 15/17 | chr3 | 158685529 | ||||||
chr3:158685583
|
G | A | 51 | a0001c0001t0003g0009a0001c0001t0003g0012a0001c0001t0003g0026others(48): Show | 57 | HG00280.hp2 HG00423.hp1 HG00609.hp2 others(54): Show |
intron_variant | MODIFIER | c.1909+915G>A | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 15/17 | chr3 | 158685583 | ||||||
chr3:158685596
|
G | A | 1 | a0001c0004t0024g0283 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.1909+928G>A | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 15/17 | chr3 | 158685596 | ||||||
chr3:158685696
|
T | C | 28 | a0001c0001t0004g0002a0001c0001t0004g0013a0001c0001t0004g0014others(25): Show | 38 | HG00323.hp1 HG00597.hp2 HG00642.hp2 others(35): Show |
intron_variant | MODIFIER | c.1909+1028T>C | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 15/17 | chr3 | 158685696 | ||||||
chr3:158685710
|
G | A | 1 | a0002c0002t0001g0112 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.1909+1042G>A | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 15/17 | chr3 | 158685710 | ||||||
chr3:158685750
|
G | A | 141 | a0001c0001t0003g0009a0001c0001t0003g0012a0001c0001t0003g0026others(138): Show | 159 | HG00280.hp2 HG00323.hp1 HG00423.hp1 others(156): Show |
intron_variant | MODIFIER | c.1909+1082G>A | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 15/17 | chr3 | 158685750 | ||||||
chr3:158685823
|
C | T | 1 | a0001c0001t0015g0016 | 2 | HG03490.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.1909+1155C>T | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 15/17 | chr3 | 158685823 | ||||||
chr3:158685941
|
G | A | 1 | a0001c0001t0003g0214 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.1909+1273G>A | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 15/17 | chr3 | 158685941 | ||||||
chr3:158685961
|
T | G | 5 | a0002c0002t0001g0011a0002c0002t0001g0024a0002c0002t0001g0154others(2): Show | 8 | HG01346.hp1 HG01433.hp1 HG01496.hp1 others(5): Show |
intron_variant | MODIFIER | c.1909+1293T>G | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 15/17 | chr3 | 158685961 | ||||||
chr3:158686103
|
T | C | 2 | a0001c0001t0004g0263a0001c0001t0004g0276 | 2 | HG02280.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.1909+1435T>C | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 15/17 | chr3 | 158686103 | ||||||
chr3:158686155
|
A | G | 141 | a0001c0001t0003g0009a0001c0001t0003g0012a0001c0001t0003g0026others(138): Show | 159 | HG00280.hp2 HG00323.hp1 HG00423.hp1 others(156): Show |
intron_variant | MODIFIER | c.1909+1487A>G | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 15/17 | chr3 | 158686155 | ||||||
chr3:158686217
|
G | T | 1 | a0001c0001t0023g0306 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.1909+1549G>T | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 15/17 | chr3 | 158686217 | ||||||
chr3:158686397
|
T | TA | 137 | a0001c0001t0003g0009a0001c0001t0003g0012a0001c0001t0003g0026others(134): Show | 155 | HG00280.hp2 HG00323.hp1 HG00423.hp1 others(152): Show |
intron_variant | MODIFIER | c.1909+1736dupA | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 15/17 | INFO_REALIGN_3_PRIME | chr3 | 158686397 | |||||
chr3:158686452
|
C | G | 1 | a0001c0001t0003g0198 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.1909+1784C>G | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 15/17 | chr3 | 158686452 | ||||||
chr3:158686478
|
C | T | 201 | a0001c0001t0002g0001a0001c0001t0002g0005a0001c0001t0002g0015others(198): Show | 232 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(229): Show |
intron_variant | MODIFIER | c.1909+1810C>T | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 15/17 | chr3 | 158686478 | ||||||
chr3:158686551
|
A | G | 3 | a0001c0001t0014g0178a0001c0001t0014g0179a0001c0001t0014g0296 | 3 | HG03098.hp2 HG03486.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.1909+1883A>G | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 15/17 | chr3 | 158686551 | ||||||
chr3:158686651
|
ATAT | A | 141 | a0001c0001t0003g0009a0001c0001t0003g0012a0001c0001t0003g0026others(138): Show | 159 | HG00280.hp2 HG00323.hp1 HG00423.hp1 others(156): Show |
intron_variant | MODIFIER | c.1909+1989_1909+199 others(7): Show |
GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 15/17 | INFO_REALIGN_3_PRIME | chr3 | 158686651 | |||||
chr3:158686721
|
G | GT | 69 | a0001c0001t0002g0001a0001c0001t0002g0005a0001c0001t0002g0031others(66): Show | 84 | HG00140.hp1 HG00280.hp1 HG00423.hp2 others(81): Show |
intron_variant | MODIFIER | c.1909+2076dupT | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 15/17 | INFO_REALIGN_3_PRIME | chr3 | 158686721 | |||||
chr3:158686721
|
G | GTT | 29 | a0001c0001t0002g0015a0001c0001t0002g0032a0001c0001t0002g0039others(26): Show | 30 | HG01109.hp2 HG01175.hp2 HG01243.hp1 others(27): Show |
intron_variant | MODIFIER | c.1909+2075_1909+207 others(6): Show |
GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 15/17 | INFO_REALIGN_3_PRIME | chr3 | 158686721 | |||||
chr3:158686721
|
G | GTTT | 71 | a0001c0001t0003g0009a0001c0001t0003g0012a0001c0001t0003g0026others(68): Show | 77 | HG00280.hp2 HG00423.hp1 HG00609.hp2 others(74): Show |
intron_variant | MODIFIER | c.1909+2074_1909+207 others(7): Show |
GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 15/17 | INFO_REALIGN_3_PRIME | chr3 | 158686721 | |||||
chr3:158686721
|
G | GTTTT | 48 | a0001c0001t0003g0184a0001c0001t0003g0186a0001c0001t0003g0191others(45): Show | 60 | HG00323.hp1 HG00597.hp2 HG00642.hp2 others(57): Show |
intron_variant | MODIFIER | c.1909+2073_1909+207 others(8): Show |
GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 15/17 | INFO_REALIGN_3_PRIME | chr3 | 158686721 | |||||
chr3:158686721
|
G | GTTTTT | 7 | a0001c0001t0004g0030a0001c0001t0004g0180a0001c0001t0004g0232others(4): Show | 7 | HG02818.hp1 HG03486.hp1 HG03688.hp1 others(4): Show |
intron_variant | MODIFIER | c.1909+2072_1909+207 others(9): Show |
GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 15/17 | INFO_REALIGN_3_PRIME | chr3 | 158686721 | |||||
chr3:158686721
|
GT | G | 7 | a0002c0002t0001g0004a0002c0002t0001g0092a0002c0002t0001g0099others(4): Show | 11 | HG00639.hp2 HG00735.hp1 HG00738.hp1 others(8): Show |
intron_variant | MODIFIER | c.1909+2076delT | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 15/17 | INFO_REALIGN_3_PRIME | chr3 | 158686721 | |||||
chr3:158686787
|
C | T | 1 | a0001c0001t0003g0186 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1909+2119C>T | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 15/17 | chr3 | 158686787 | ||||||
chr3:158686890
|
G | A | 141 | a0001c0001t0003g0009a0001c0001t0003g0012a0001c0001t0003g0026others(138): Show | 159 | HG00280.hp2 HG00323.hp1 HG00423.hp1 others(156): Show |
intron_variant | MODIFIER | c.1909+2222G>A | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 15/17 | chr3 | 158686890 | ||||||
chr3:158686969
|
G | C | 52 | a0001c0001t0004g0002a0001c0001t0004g0013a0001c0001t0004g0014others(49): Show | 63 | HG00323.hp1 HG00597.hp2 HG00642.hp2 others(60): Show |
intron_variant | MODIFIER | c.1909+2301G>C | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 15/17 | chr3 | 158686969 | ||||||
chr3:158687029
|
T | G | 141 | a0001c0001t0003g0009a0001c0001t0003g0012a0001c0001t0003g0026others(138): Show | 159 | HG00280.hp2 HG00323.hp1 HG00423.hp1 others(156): Show |
intron_variant | MODIFIER | c.1909+2361T>G | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 15/17 | chr3 | 158687029 | ||||||
chr3:158687031
|
C | A | 1 | a0001c0001t0023g0306 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.1909+2363C>A | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 15/17 | chr3 | 158687031 | ||||||
chr3:158687036
|
T | C | 2 | a0001c0001t0003g0191a0001c0001t0003g0198 | 2 | HG02572.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.1909+2368T>C | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 15/17 | chr3 | 158687036 | ||||||
chr3:158687086
|
T | C | 1 | a0002c0002t0001g0143 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.1909+2418T>C | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 15/17 | chr3 | 158687086 | ||||||
chr3:158687087
|
C | T | 1 | a0002c0002t0001g0103 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.1909+2419C>T | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 15/17 | chr3 | 158687087 | ||||||
chr3:158687156
|
C | T | 5 | a0003c0003t0007g0230a0003c0003t0007g0247a0003c0003t0007g0248others(2): Show | 5 | HG01175.hp1 HG02486.hp1 HG02630.hp2 others(2): Show |
intron_variant | MODIFIER | c.1909+2488C>T | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 15/17 | chr3 | 158687156 | ||||||
chr3:158687216
|
G | A | 1 | a0001c0001t0023g0306 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.1909+2548G>A | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 15/17 | chr3 | 158687216 | ||||||
chr3:158687428
|
C | T | 202 | a0001c0001t0002g0001a0001c0001t0002g0005a0001c0001t0002g0015others(199): Show | 233 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(230): Show |
intron_variant | MODIFIER | c.1910-2735C>T | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 15/17 | chr3 | 158687428 | ||||||
chr3:158687615
|
G | A | 60 | a0001c0001t0002g0001a0001c0001t0002g0005a0001c0001t0002g0015others(57): Show | 73 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(70): Show |
intron_variant | MODIFIER | c.1910-2548G>A | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 15/17 | chr3 | 158687615 | ||||||
chr3:158687683
|
G | A | 2 | a0001c0001t0002g0034a0001c0001t0002g0042 | 2 | HG00140.hp1 HG01978.hp1 |
intron_variant | MODIFIER | c.1910-2480G>A | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 15/17 | chr3 | 158687683 | ||||||
chr3:158687694
|
C | G | 1 | a0002c0002t0001g0112 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.1910-2469C>G | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 15/17 | chr3 | 158687694 | ||||||
chr3:158687720
|
C | T | 1 | a0001c0001t0004g0238 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.1910-2443C>T | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 15/17 | chr3 | 158687720 | ||||||
chr3:158687780
|
A | G | 1 | a0002c0002t0001g0136 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.1910-2383A>G | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 15/17 | chr3 | 158687780 | ||||||
chr3:158687829
|
G | A | 51 | a0001c0001t0003g0009a0001c0001t0003g0012a0001c0001t0003g0026others(48): Show | 57 | HG00280.hp2 HG00423.hp1 HG00609.hp2 others(54): Show |
intron_variant | MODIFIER | c.1910-2334G>A | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 15/17 | chr3 | 158687829 | ||||||
chr3:158687907
|
C | A | 8 | a0001c0001t0007g0255a0003c0003t0007g0230a0003c0003t0007g0235others(5): Show | 8 | HG01175.hp1 HG02257.hp2 HG02486.hp1 others(5): Show |
intron_variant | MODIFIER | c.1910-2256C>A | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 15/17 | chr3 | 158687907 | ||||||
chr3:158687916
|
G | A | 28 | a0001c0001t0004g0002a0001c0001t0004g0013a0001c0001t0004g0014others(25): Show | 38 | HG00323.hp1 HG00597.hp2 HG00642.hp2 others(35): Show |
intron_variant | MODIFIER | c.1910-2247G>A | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 15/17 | chr3 | 158687916 | ||||||
chr3:158687925
|
T | G | 12 | a0001c0001t0009g0289a0001c0001t0009g0290a0001c0001t0009g0291others(9): Show | 12 | HG01884.hp1 HG02258.hp2 HG02622.hp2 others(9): Show |
intron_variant | MODIFIER | c.1910-2238T>G | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 15/17 | chr3 | 158687925 | ||||||
chr3:158687941
|
A | G | 7 | a0001c0001t0004g0029a0001c0001t0004g0233a0001c0001t0004g0244others(4): Show | 8 | HG02257.hp1 HG02258.hp1 HG02630.hp1 others(5): Show |
intron_variant | MODIFIER | c.1910-2222A>G | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 15/17 | chr3 | 158687941 | ||||||
chr3:158687977
|
G | A | 115 | a0001c0001t0003g0009a0001c0001t0003g0012a0001c0001t0003g0026others(112): Show | 132 | HG00280.hp2 HG00323.hp1 HG00423.hp1 others(129): Show |
intron_variant | MODIFIER | c.1910-2186G>A | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 15/17 | chr3 | 158687977 | ||||||
chr3:158687986
|
T | C | 23 | a0001c0001t0005g0277a0001c0001t0005g0278a0001c0001t0005g0279others(20): Show | 24 | HG01175.hp1 HG01891.hp1 HG01891.hp2 others(21): Show |
intron_variant | MODIFIER | c.1910-2177T>C | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 15/17 | chr3 | 158687986 | ||||||
chr3:158688084
|
G | A | 51 | a0001c0001t0003g0009a0001c0001t0003g0012a0001c0001t0003g0026others(48): Show | 57 | HG00280.hp2 HG00423.hp1 HG00609.hp2 others(54): Show |
intron_variant | MODIFIER | c.1910-2079G>A | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 15/17 | chr3 | 158688084 | ||||||
chr3:158688110
|
A | G | 202 | a0001c0001t0002g0001a0001c0001t0002g0005a0001c0001t0002g0015others(199): Show | 233 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(230): Show |
intron_variant | MODIFIER | c.1910-2053A>G | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 15/17 | chr3 | 158688110 | ||||||
chr3:158688167
|
T | G | 1 | a0001c0001t0027g0236 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.1910-1996T>G | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 15/17 | chr3 | 158688167 | ||||||
chr3:158688190
|
A | T | 1 | a0002c0002t0001g0171 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.1910-1973A>T | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 15/17 | chr3 | 158688190 | ||||||
chr3:158688216
|
C | T | 26 | a0001c0001t0005g0277a0001c0001t0005g0278a0001c0001t0005g0279others(23): Show | 27 | HG01175.hp1 HG01243.hp1 HG01891.hp1 others(24): Show |
intron_variant | MODIFIER | c.1910-1947C>T | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 15/17 | chr3 | 158688216 | ||||||
chr3:158688257
|
T | C | 2 | a0001c0001t0002g0049a0001c0001t0002g0066 | 2 | HG02698.hp2 HG03704.hp2 |
intron_variant | MODIFIER | c.1910-1906T>C | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 15/17 | chr3 | 158688257 | ||||||
chr3:158688286
|
G | A | 60 | a0001c0001t0002g0001a0001c0001t0002g0005a0001c0001t0002g0015others(57): Show | 73 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(70): Show |
intron_variant | MODIFIER | c.1910-1877G>A | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 15/17 | chr3 | 158688286 | ||||||
chr3:158688385
|
G | A | 1 | a0001c0001t0002g0035 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.1910-1778G>A | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 15/17 | chr3 | 158688385 | ||||||
chr3:158688672
|
T | G | 141 | a0001c0001t0003g0009a0001c0001t0003g0012a0001c0001t0003g0026others(138): Show | 159 | HG00280.hp2 HG00323.hp1 HG00423.hp1 others(156): Show |
intron_variant | MODIFIER | c.1910-1491T>G | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 15/17 | chr3 | 158688672 | ||||||
chr3:158688750
|
A | C | 1 | a0001c0001t0018g0294 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.1910-1413A>C | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 15/17 | chr3 | 158688750 | ||||||
chr3:158688849
|
G | T | 1 | a0002c0002t0001g0135 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.1910-1314G>T | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 15/17 | chr3 | 158688849 | ||||||
chr3:158688934
|
G | A | 1 | a0001c0001t0023g0306 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.1910-1229G>A | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 15/17 | chr3 | 158688934 | ||||||
chr3:158689126
|
A | G | 202 | a0001c0001t0002g0001a0001c0001t0002g0005a0001c0001t0002g0015others(199): Show | 233 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(230): Show |
intron_variant | MODIFIER | c.1910-1037A>G | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 15/17 | chr3 | 158689126 | ||||||
chr3:158689153
|
T | C | 1 | a0001c0004t0024g0283 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.1910-1010T>C | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 15/17 | chr3 | 158689153 | ||||||
chr3:158689397
|
A | C | 51 | a0001c0001t0003g0009a0001c0001t0003g0012a0001c0001t0003g0026others(48): Show | 57 | HG00280.hp2 HG00423.hp1 HG00609.hp2 others(54): Show |
intron_variant | MODIFIER | c.1910-766A>C | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 15/17 | chr3 | 158689397 | ||||||
chr3:158689442
|
G | A | 1 | a0002c0002t0001g0095 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.1910-721G>A | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 15/17 | chr3 | 158689442 | ||||||
chr3:158689442
|
G | T | 51 | a0001c0001t0003g0009a0001c0001t0003g0012a0001c0001t0003g0026others(48): Show | 57 | HG00280.hp2 HG00423.hp1 HG00609.hp2 others(54): Show |
intron_variant | MODIFIER | c.1910-721G>T | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 15/17 | chr3 | 158689442 | ||||||
chr3:158689519
|
A | G | 1 | a0002c0002t0001g0142 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.1910-644A>G | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 15/17 | chr3 | 158689519 | ||||||
chr3:158689544
|
C | T | 141 | a0001c0001t0003g0009a0001c0001t0003g0012a0001c0001t0003g0026others(138): Show | 159 | HG00280.hp2 HG00323.hp1 HG00423.hp1 others(156): Show |
intron_variant | MODIFIER | c.1910-619C>T | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 15/17 | chr3 | 158689544 | ||||||
chr3:158689581
|
C | G | 1 | a0001c0001t0002g0039 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.1910-582C>G | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 15/17 | chr3 | 158689581 | ||||||
chr3:158689595
|
C | T | 13 | a0001c0001t0005g0277a0001c0001t0005g0278a0001c0001t0005g0279others(10): Show | 13 | HG01891.hp1 HG01891.hp2 HG02055.hp1 others(10): Show |
intron_variant | MODIFIER | c.1910-568C>T | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 15/17 | chr3 | 158689595 | ||||||
chr3:158689641
|
A | G | 202 | a0001c0001t0002g0001a0001c0001t0002g0005a0001c0001t0002g0015others(199): Show | 233 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(230): Show |
intron_variant | MODIFIER | c.1910-522A>G | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 15/17 | chr3 | 158689641 | ||||||
chr3:158689660
|
C | T | 2 | a0002c0002t0001g0107a0002c0002t0001g0109 | 2 | HG00639.hp2 HG00642.hp1 |
intron_variant | MODIFIER | c.1910-503C>T | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 15/17 | chr3 | 158689660 | ||||||
chr3:158689728
|
T | C | 2 | a0001c0001t0003g0192a0001c0001t0003g0223 | 2 | HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.1910-435T>C | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 15/17 | chr3 | 158689728 | ||||||
chr3:158689747
|
C | CA | 20 | a0001c0001t0003g0197a0001c0001t0003g0215a0001c0001t0009g0289others(17): Show | 21 | HG01884.hp1 HG02145.hp1 HG02258.hp2 others(18): Show |
intron_variant | MODIFIER | c.1910-400dupA | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 15/17 | INFO_REALIGN_3_PRIME | chr3 | 158689747 | |||||
chr3:158689747
|
CA | C | 60 | a0001c0001t0002g0001a0001c0001t0002g0005a0001c0001t0002g0015others(57): Show | 73 | HG00099.hp2 HG00140.hp1 HG00423.hp2 others(70): Show |
intron_variant | MODIFIER | c.1910-400delA | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 15/17 | INFO_REALIGN_3_PRIME | chr3 | 158689747 | |||||
chr3:158689976
|
T | C | 1 | a0001c0001t0003g0195 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.1910-187T>C | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 15/17 | chr3 | 158689976 | ||||||
chr3:158690034
|
G | A | 1 | a0001c0001t0002g0035 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.1910-129G>A | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 15/17 | chr3 | 158690034 | ||||||
chr3:158690141
|
CT | C | 7 | a0001c0001t0002g0053a0001c0001t0003g0190a0001c0001t0003g0210others(4): Show | 7 | HG01069.hp1 NA18939.hp1 NA18962.hp1 others(4): Show |
splice_region_variant&intron_variant | LOW | c.1910-8delT | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 15/17 | INFO_REALIGN_3_PRIME | chr3 | 158690141 | |||||
chr3:158690334
|
T | G | 1 | a0001c0001t0023g0306 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.2070+11T>G | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 16/17 | chr3 | 158690334 | ||||||
chr3:158690681
|
T | A | 1 | a0001c0004t0024g0283 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.2070+358T>A | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 16/17 | chr3 | 158690681 | ||||||
chr3:158690836
|
T | G | 1 | a0002c0002t0001g0171 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.2071-303T>G | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 16/17 | chr3 | 158690836 | ||||||
chr3:158690895
|
G | A | 2 | a0001c0001t0002g0040a0001c0001t0002g0075 | 2 | NA18992.hp2 NA19079.hp1 |
intron_variant | MODIFIER | c.2071-244G>A | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 16/17 | chr3 | 158690895 | ||||||
chr3:158690914
|
G | A | 1 | a0002c0002t0001g0163 | 1 | NA18957.hp1 | intron_variant | MODIFIER | c.2071-225G>A | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 16/17 | chr3 | 158690914 | ||||||
chr3:158691090
|
A | G | 1 | a0001c0001t0008g0270 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.2071-49A>G | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 16/17 | chr3 | 158691090 | ||||||
chr3:158691119
|
T | C | 1 | a0001c0001t0003g0196 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.2071-20T>C | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 16/17 | chr3 | 158691119 | ||||||
chr3:158691122
|
A | G | 6 | a0001c0001t0009g0289a0001c0001t0009g0290a0001c0001t0009g0291others(3): Show | 6 | HG01884.hp1 HG02258.hp2 HG02622.hp2 others(3): Show |
intron_variant | MODIFIER | c.2071-17A>G | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 16/17 | chr3 | 158691122 | ||||||
chr3:158691304
|
C | CA | 139 | a0001c0001t0003g0009a0001c0001t0003g0012a0001c0001t0003g0026others(136): Show | 157 | HG00280.hp2 HG00323.hp1 HG00423.hp1 others(154): Show |
intron_variant | MODIFIER | c.2125-26dupA | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 17/17 | INFO_REALIGN_3_PRIME | chr3 | 158691304 | |||||
chr3:158691311
|
C | A | 1 | a0001c0004t0026g0305 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.2125-25C>A | GFM1 | ENSG00000168827.15 | transcript | ENST00000486715.6 | protein_coding | 17/17 | chr3 | 158691311 |