geneid | 122786 |
---|---|
ensemblid | ENSG00000139926.16 |
hgncid | 19839 |
symbol | FRMD6 |
name | FERM domain containing 6 |
refseq_nuc | NM_001267046.2 |
refseq_prot | NP_001253975.1 |
ensembl_nuc | ENST00000344768.10 |
ensembl_prot | ENSP00000343899.6 |
mane_status | MANE Select |
chr | chr14 |
start | 51651910 |
end | 51730727 |
strand | + |
ver | v1.2 |
region | chr14:51651910-51730727 |
region5000 | chr14:51646910-51735727 |
regionname0 | FRMD6_chr14_51651910_51730727 |
regionname5000 | FRMD6_chr14_51646910_51735727 |
ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 1/1 | 622 | 385 | 86 | 70 | 179 | 16 | 32 | 139 | FRMD6_chr14_51646910_51735727 | FRMD6 | copy fasta | chr14 | 51646910 | 51735727 |
a0002 | 0/0 | 622 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | FRMD6_chr14_51646910_51735727 | FRMD6 | copy fasta | chr14 | 51646910 | 51735727 |
a0003 | 0/0 | 622 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | FRMD6_chr14_51646910_51735727 | FRMD6 | copy fasta | chr14 | 51646910 | 51735727 |
a0004 | 0/0 | 622 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | FRMD6_chr14_51646910_51735727 | FRMD6 | copy fasta | chr14 | 51646910 | 51735727 |
a0005 | 0/0 | 622 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | FRMD6_chr14_51646910_51735727 | FRMD6 | copy fasta | chr14 | 51646910 | 51735727 |
chapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
c0001 | 0/0 | 1869 | 124 | 32 | 16 | 62 | 6 | 8 | FRMD6_chr14_51646910_51735727 | FRMD6 | copy fasta | chr14 | 51646910 | 51735727 |
c0002 | 1/0 | 1869 | 111 | 22 | 29 | 41 | 4 | 14 | FRMD6_chr14_51646910_51735727 | FRMD6 | copy fasta | chr14 | 51646910 | 51735727 |
c0003 | 0/1 | 1869 | 97 | 12 | 19 | 54 | 4 | 7 | FRMD6_chr14_51646910_51735727 | FRMD6 | copy fasta | chr14 | 51646910 | 51735727 |
c0004 | 0/0 | 1869 | 21 | 9 | 4 | 4 | 1 | 3 | FRMD6_chr14_51646910_51735727 | FRMD6 | copy fasta | chr14 | 51646910 | 51735727 |
c0005 | 0/0 | 1869 | 14 | 0 | 0 | 14 | 0 | 0 | FRMD6_chr14_51646910_51735727 | FRMD6 | copy fasta | chr14 | 51646910 | 51735727 |
c0006 | 0/0 | 1869 | 10 | 8 | 2 | 0 | 0 | 0 | FRMD6_chr14_51646910_51735727 | FRMD6 | copy fasta | chr14 | 51646910 | 51735727 |
c0007 | 0/0 | 1869 | 2 | 2 | 0 | 0 | 0 | 0 | FRMD6_chr14_51646910_51735727 | FRMD6 | copy fasta | chr14 | 51646910 | 51735727 |
c0008 | 0/0 | 1869 | 2 | 2 | 0 | 0 | 0 | 0 | FRMD6_chr14_51646910_51735727 | FRMD6 | copy fasta | chr14 | 51646910 | 51735727 |
c0009 | 0/0 | 1869 | 2 | 0 | 0 | 2 | 0 | 0 | FRMD6_chr14_51646910_51735727 | FRMD6 | copy fasta | chr14 | 51646910 | 51735727 |
c0010 | 0/0 | 1869 | 1 | 1 | 0 | 0 | 0 | 0 | FRMD6_chr14_51646910_51735727 | FRMD6 | copy fasta | chr14 | 51646910 | 51735727 |
c0011 | 0/0 | 1869 | 1 | 0 | 0 | 1 | 0 | 0 | FRMD6_chr14_51646910_51735727 | FRMD6 | copy fasta | chr14 | 51646910 | 51735727 |
c0012 | 0/0 | 1869 | 1 | 1 | 0 | 0 | 0 | 0 | FRMD6_chr14_51646910_51735727 | FRMD6 | copy fasta | chr14 | 51646910 | 51735727 |
c0013 | 0/0 | 1869 | 1 | 1 | 0 | 0 | 0 | 0 | FRMD6_chr14_51646910_51735727 | FRMD6 | copy fasta | chr14 | 51646910 | 51735727 |
c0014 | 0/0 | 1869 | 1 | 0 | 0 | 1 | 0 | 0 | FRMD6_chr14_51646910_51735727 | FRMD6 | copy fasta | chr14 | 51646910 | 51735727 |
c0015 | 0/0 | 1869 | 1 | 0 | 0 | 0 | 1 | 0 | FRMD6_chr14_51646910_51735727 | FRMD6 | copy fasta | chr14 | 51646910 | 51735727 |
c0016 | 0/0 | 1869 | 1 | 0 | 0 | 1 | 0 | 0 | FRMD6_chr14_51646910_51735727 | FRMD6 | copy fasta | chr14 | 51646910 | 51735727 |
thapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
t0001 | 1/1 | 2932 | 234 | 47 | 43 | 110 | 9 | 23 | FRMD6_chr14_51646910_51735727 | FRMD6 | copy fasta | chr14 | 51646910 | 51735727 |
t0002 | 0/0 | 2933 | 110 | 21 | 15 | 60 | 6 | 8 | FRMD6_chr14_51646910_51735727 | FRMD6 | copy fasta | chr14 | 51646910 | 51735727 |
t0003 | 0/0 | 2932 | 9 | 8 | 1 | 0 | 0 | 0 | FRMD6_chr14_51646910_51735727 | FRMD6 | copy fasta | chr14 | 51646910 | 51735727 |
t0004 | 0/0 | 2932 | 5 | 0 | 4 | 0 | 1 | 0 | FRMD6_chr14_51646910_51735727 | FRMD6 | copy fasta | chr14 | 51646910 | 51735727 |
t0005 | 0/0 | 2932 | 4 | 0 | 0 | 4 | 0 | 0 | FRMD6_chr14_51646910_51735727 | FRMD6 | copy fasta | chr14 | 51646910 | 51735727 |
t0006 | 0/0 | 2933 | 3 | 2 | 1 | 0 | 0 | 0 | FRMD6_chr14_51646910_51735727 | FRMD6 | copy fasta | chr14 | 51646910 | 51735727 |
t0007 | 0/0 | 2933 | 3 | 0 | 3 | 0 | 0 | 0 | FRMD6_chr14_51646910_51735727 | FRMD6 | copy fasta | chr14 | 51646910 | 51735727 |
t0008 | 0/0 | 2932 | 3 | 0 | 0 | 3 | 0 | 0 | FRMD6_chr14_51646910_51735727 | FRMD6 | copy fasta | chr14 | 51646910 | 51735727 |
t0009 | 0/0 | 2932 | 2 | 2 | 0 | 0 | 0 | 0 | FRMD6_chr14_51646910_51735727 | FRMD6 | copy fasta | chr14 | 51646910 | 51735727 |
t0010 | 0/0 | 2933 | 2 | 0 | 0 | 2 | 0 | 0 | FRMD6_chr14_51646910_51735727 | FRMD6 | copy fasta | chr14 | 51646910 | 51735727 |
t0011 | 0/0 | 2933 | 2 | 2 | 0 | 0 | 0 | 0 | FRMD6_chr14_51646910_51735727 | FRMD6 | copy fasta | chr14 | 51646910 | 51735727 |
t0012 | 0/0 | 2932 | 1 | 1 | 0 | 0 | 0 | 0 | FRMD6_chr14_51646910_51735727 | FRMD6 | copy fasta | chr14 | 51646910 | 51735727 |
t0013 | 0/0 | 2932 | 1 | 1 | 0 | 0 | 0 | 0 | FRMD6_chr14_51646910_51735727 | FRMD6 | copy fasta | chr14 | 51646910 | 51735727 |
t0014 | 0/0 | 2932 | 1 | 0 | 0 | 0 | 0 | 1 | FRMD6_chr14_51646910_51735727 | FRMD6 | copy fasta | chr14 | 51646910 | 51735727 |
t0015 | 0/0 | 2932 | 1 | 0 | 1 | 0 | 0 | 0 | FRMD6_chr14_51646910_51735727 | FRMD6 | copy fasta | chr14 | 51646910 | 51735727 |
t0016 | 0/0 | 2932 | 1 | 1 | 0 | 0 | 0 | 0 | FRMD6_chr14_51646910_51735727 | FRMD6 | copy fasta | chr14 | 51646910 | 51735727 |
t0017 | 0/0 | 2932 | 1 | 0 | 1 | 0 | 0 | 0 | FRMD6_chr14_51646910_51735727 | FRMD6 | copy fasta | chr14 | 51646910 | 51735727 |
t0018 | 0/0 | 2933 | 1 | 1 | 0 | 0 | 0 | 0 | FRMD6_chr14_51646910_51735727 | FRMD6 | copy fasta | chr14 | 51646910 | 51735727 |
t0019 | 0/0 | 2933 | 1 | 1 | 0 | 0 | 0 | 0 | FRMD6_chr14_51646910_51735727 | FRMD6 | copy fasta | chr14 | 51646910 | 51735727 |
t0020 | 0/0 | 2933 | 1 | 0 | 0 | 1 | 0 | 0 | FRMD6_chr14_51646910_51735727 | FRMD6 | copy fasta | chr14 | 51646910 | 51735727 |
t0021 | 0/0 | 2933 | 1 | 1 | 0 | 0 | 0 | 0 | FRMD6_chr14_51646910_51735727 | FRMD6 | copy fasta | chr14 | 51646910 | 51735727 |
t0022 | 0/0 | 2932 | 1 | 0 | 1 | 0 | 0 | 0 | FRMD6_chr14_51646910_51735727 | FRMD6 | copy fasta | chr14 | 51646910 | 51735727 |
t0023 | 0/0 | 2933 | 1 | 1 | 0 | 0 | 0 | 0 | FRMD6_chr14_51646910_51735727 | FRMD6 | copy fasta | chr14 | 51646910 | 51735727 |
t0024 | 0/0 | 2933 | 1 | 1 | 0 | 0 | 0 | 0 | FRMD6_chr14_51646910_51735727 | FRMD6 | copy fasta | chr14 | 51646910 | 51735727 |
ghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
g0001 | 0/0 | 6 | 0 | 0 | 5 | 0 | 1 | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
g0002 | 0/0 | 6 | 0 | 0 | 6 | 0 | 0 | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
g0003 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
g0004 | 0/0 | 5 | 0 | 0 | 3 | 0 | 2 | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
g0005 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
g0006 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
g0007 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
g0008 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
g0009 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
g0010 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
g0011 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
g0012 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
g0013 | 0/0 | 3 | 0 | 2 | 0 | 1 | 0 | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
g0014 | 0/0 | 3 | 0 | 1 | 0 | 0 | 2 | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
g0015 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
g0016 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
g0017 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
g0018 | 0/0 | 3 | 2 | 0 | 0 | 0 | 1 | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
g0019 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
g0020 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
g0021 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
g0022 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
g0023 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
g0024 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
g0025 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
g0026 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
g0027 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
g0028 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
g0029 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
g0030 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
g0031 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
g0032 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
g0033 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
g0034 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
g0035 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
g0036 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
g0037 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
g0038 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
g0039 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
g0040 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
g0041 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
g0042 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
g0043 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
g0044 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
g0045 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
g0046 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
g0048 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
g0049 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
g0050 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
g0051 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
g0060 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
g0064 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
g0065 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
g0066 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
g0067 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
g0068 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
g0069 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
g0074 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
g0087 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
g0095 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
g0097 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
g0100 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
g0102 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
g0108 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
g0120 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
g0123 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
g0133 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
g0159 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
g0163 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
g0164 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
g0167 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
g0170 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
g0173 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
g0174 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
g0175 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
g0176 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
g0184 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
g0188 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
g0189 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
g0191 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
g0192 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
g0195 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
g0196 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
g0203 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
g0204 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
g0205 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
g0211 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
g0213 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
g0219 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
g0221 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
g0222 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
g0223 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
g0225 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
g0226 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
g0227 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
g0228 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
g0229 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
g0230 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
g0231 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
g0234 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
g0236 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
g0238 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
g0240 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
g0242 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
g0243 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
g0245 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
g0246 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
g0247 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
g0253 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
g0254 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
g0263 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
g0264 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
g0265 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
g0266 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
g0269 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
g0270 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
g0271 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
g0274 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
g0279 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
g0286 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
g0289 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
g0290 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
g0291 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
g0299 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
g0302 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
g0303 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
g0304 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
g0305 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
g0306 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
g0307 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
g0308 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
g0309 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
g0310 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
g0311 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
g0312 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
g0313 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
g0314 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
g0315 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
achapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 0/0 | 1869 | 124 | 32 | 16 | 62 | 6 | 8 | FRMD6_chr14_51646910_51735727 | FRMD6 | copy fasta | chr14 | 51646910 | 51735727 |
a0001c0002 | 1/0 | 1869 | 111 | 22 | 29 | 41 | 4 | 14 | FRMD6_chr14_51646910_51735727 | FRMD6 | copy fasta | chr14 | 51646910 | 51735727 |
a0001c0003 | 0/1 | 1869 | 97 | 12 | 19 | 54 | 4 | 7 | FRMD6_chr14_51646910_51735727 | FRMD6 | copy fasta | chr14 | 51646910 | 51735727 |
a0001c0004 | 0/0 | 1869 | 21 | 9 | 4 | 4 | 1 | 3 | FRMD6_chr14_51646910_51735727 | FRMD6 | copy fasta | chr14 | 51646910 | 51735727 |
a0001c0005 | 0/0 | 1869 | 14 | 0 | 0 | 14 | 0 | 0 | FRMD6_chr14_51646910_51735727 | FRMD6 | copy fasta | chr14 | 51646910 | 51735727 |
a0001c0006 | 0/0 | 1869 | 10 | 8 | 2 | 0 | 0 | 0 | FRMD6_chr14_51646910_51735727 | FRMD6 | copy fasta | chr14 | 51646910 | 51735727 |
a0001c0007 | 0/0 | 1869 | 2 | 2 | 0 | 0 | 0 | 0 | FRMD6_chr14_51646910_51735727 | FRMD6 | copy fasta | chr14 | 51646910 | 51735727 |
a0001c0009 | 0/0 | 1869 | 2 | 0 | 0 | 2 | 0 | 0 | FRMD6_chr14_51646910_51735727 | FRMD6 | copy fasta | chr14 | 51646910 | 51735727 |
a0001c0011 | 0/0 | 1869 | 1 | 0 | 0 | 1 | 0 | 0 | FRMD6_chr14_51646910_51735727 | FRMD6 | copy fasta | chr14 | 51646910 | 51735727 |
a0001c0013 | 0/0 | 1869 | 1 | 1 | 0 | 0 | 0 | 0 | FRMD6_chr14_51646910_51735727 | FRMD6 | copy fasta | chr14 | 51646910 | 51735727 |
a0001c0014 | 0/0 | 1869 | 1 | 0 | 0 | 1 | 0 | 0 | FRMD6_chr14_51646910_51735727 | FRMD6 | copy fasta | chr14 | 51646910 | 51735727 |
a0001c0015 | 0/0 | 1869 | 1 | 0 | 0 | 0 | 1 | 0 | FRMD6_chr14_51646910_51735727 | FRMD6 | copy fasta | chr14 | 51646910 | 51735727 |
a0002c0008 | 0/0 | 1869 | 2 | 2 | 0 | 0 | 0 | 0 | FRMD6_chr14_51646910_51735727 | FRMD6 | copy fasta | chr14 | 51646910 | 51735727 |
a0003c0010 | 0/0 | 1869 | 1 | 1 | 0 | 0 | 0 | 0 | FRMD6_chr14_51646910_51735727 | FRMD6 | copy fasta | chr14 | 51646910 | 51735727 |
a0004c0012 | 0/0 | 1869 | 1 | 1 | 0 | 0 | 0 | 0 | FRMD6_chr14_51646910_51735727 | FRMD6 | copy fasta | chr14 | 51646910 | 51735727 |
a0005c0016 | 0/0 | 1869 | 1 | 0 | 0 | 1 | 0 | 0 | FRMD6_chr14_51646910_51735727 | FRMD6 | copy fasta | chr14 | 51646910 | 51735727 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 0/0 | 4800 | 5 | 3 | 0 | 1 | 0 | 1 | FRMD6_chr14_51646910_51735727 | FRMD6 | copy fasta | chr14 | 51646910 | 51735727 |
a0001c0001t0002 | 0/0 | 4801 | 103 | 20 | 12 | 58 | 6 | 7 | FRMD6_chr14_51646910_51735727 | FRMD6 | copy fasta | chr14 | 51646910 | 51735727 |
a0001c0001t0006 | 0/0 | 4801 | 3 | 2 | 1 | 0 | 0 | 0 | FRMD6_chr14_51646910_51735727 | FRMD6 | copy fasta | chr14 | 51646910 | 51735727 |
a0001c0001t0007 | 0/0 | 4801 | 3 | 0 | 3 | 0 | 0 | 0 | FRMD6_chr14_51646910_51735727 | FRMD6 | copy fasta | chr14 | 51646910 | 51735727 |
a0001c0001t0010 | 0/0 | 4801 | 2 | 0 | 0 | 2 | 0 | 0 | FRMD6_chr14_51646910_51735727 | FRMD6 | copy fasta | chr14 | 51646910 | 51735727 |
a0001c0001t0011 | 0/0 | 4801 | 2 | 2 | 0 | 0 | 0 | 0 | FRMD6_chr14_51646910_51735727 | FRMD6 | copy fasta | chr14 | 51646910 | 51735727 |
a0001c0001t0018 | 0/0 | 4801 | 1 | 1 | 0 | 0 | 0 | 0 | FRMD6_chr14_51646910_51735727 | FRMD6 | copy fasta | chr14 | 51646910 | 51735727 |
a0001c0001t0019 | 0/0 | 4801 | 1 | 1 | 0 | 0 | 0 | 0 | FRMD6_chr14_51646910_51735727 | FRMD6 | copy fasta | chr14 | 51646910 | 51735727 |
a0001c0001t0020 | 0/0 | 4801 | 1 | 0 | 0 | 1 | 0 | 0 | FRMD6_chr14_51646910_51735727 | FRMD6 | copy fasta | chr14 | 51646910 | 51735727 |
a0001c0001t0021 | 0/0 | 4801 | 1 | 1 | 0 | 0 | 0 | 0 | FRMD6_chr14_51646910_51735727 | FRMD6 | copy fasta | chr14 | 51646910 | 51735727 |
a0001c0001t0023 | 0/0 | 4801 | 1 | 1 | 0 | 0 | 0 | 0 | FRMD6_chr14_51646910_51735727 | FRMD6 | copy fasta | chr14 | 51646910 | 51735727 |
a0001c0001t0024 | 0/0 | 4801 | 1 | 1 | 0 | 0 | 0 | 0 | FRMD6_chr14_51646910_51735727 | FRMD6 | copy fasta | chr14 | 51646910 | 51735727 |
a0001c0002t0001 | 1/0 | 4800 | 96 | 21 | 22 | 37 | 3 | 12 | FRMD6_chr14_51646910_51735727 | FRMD6 | copy fasta | chr14 | 51646910 | 51735727 |
a0001c0002t0002 | 0/0 | 4801 | 3 | 0 | 1 | 1 | 0 | 1 | FRMD6_chr14_51646910_51735727 | FRMD6 | copy fasta | chr14 | 51646910 | 51735727 |
a0001c0002t0004 | 0/0 | 4800 | 5 | 0 | 4 | 0 | 1 | 0 | FRMD6_chr14_51646910_51735727 | FRMD6 | copy fasta | chr14 | 51646910 | 51735727 |
a0001c0002t0008 | 0/0 | 4800 | 3 | 0 | 0 | 3 | 0 | 0 | FRMD6_chr14_51646910_51735727 | FRMD6 | copy fasta | chr14 | 51646910 | 51735727 |
a0001c0002t0013 | 0/0 | 4800 | 1 | 1 | 0 | 0 | 0 | 0 | FRMD6_chr14_51646910_51735727 | FRMD6 | copy fasta | chr14 | 51646910 | 51735727 |
a0001c0002t0014 | 0/0 | 4800 | 1 | 0 | 0 | 0 | 0 | 1 | FRMD6_chr14_51646910_51735727 | FRMD6 | copy fasta | chr14 | 51646910 | 51735727 |
a0001c0002t0015 | 0/0 | 4800 | 1 | 0 | 1 | 0 | 0 | 0 | FRMD6_chr14_51646910_51735727 | FRMD6 | copy fasta | chr14 | 51646910 | 51735727 |
a0001c0002t0017 | 0/0 | 4800 | 1 | 0 | 1 | 0 | 0 | 0 | FRMD6_chr14_51646910_51735727 | FRMD6 | copy fasta | chr14 | 51646910 | 51735727 |
a0001c0003t0001 | 0/1 | 4800 | 95 | 12 | 17 | 54 | 4 | 7 | FRMD6_chr14_51646910_51735727 | FRMD6 | copy fasta | chr14 | 51646910 | 51735727 |
a0001c0003t0002 | 0/0 | 4801 | 2 | 0 | 2 | 0 | 0 | 0 | FRMD6_chr14_51646910_51735727 | FRMD6 | copy fasta | chr14 | 51646910 | 51735727 |
a0001c0004t0001 | 0/0 | 4800 | 15 | 7 | 4 | 0 | 1 | 3 | FRMD6_chr14_51646910_51735727 | FRMD6 | copy fasta | chr14 | 51646910 | 51735727 |
a0001c0004t0005 | 0/0 | 4800 | 4 | 0 | 0 | 4 | 0 | 0 | FRMD6_chr14_51646910_51735727 | FRMD6 | copy fasta | chr14 | 51646910 | 51735727 |
a0001c0004t0012 | 0/0 | 4800 | 1 | 1 | 0 | 0 | 0 | 0 | FRMD6_chr14_51646910_51735727 | FRMD6 | copy fasta | chr14 | 51646910 | 51735727 |
a0001c0004t0016 | 0/0 | 4800 | 1 | 1 | 0 | 0 | 0 | 0 | FRMD6_chr14_51646910_51735727 | FRMD6 | copy fasta | chr14 | 51646910 | 51735727 |
a0001c0005t0001 | 0/0 | 4800 | 14 | 0 | 0 | 14 | 0 | 0 | FRMD6_chr14_51646910_51735727 | FRMD6 | copy fasta | chr14 | 51646910 | 51735727 |
a0001c0006t0003 | 0/0 | 4800 | 9 | 8 | 1 | 0 | 0 | 0 | FRMD6_chr14_51646910_51735727 | FRMD6 | copy fasta | chr14 | 51646910 | 51735727 |
a0001c0006t0022 | 0/0 | 4800 | 1 | 0 | 1 | 0 | 0 | 0 | FRMD6_chr14_51646910_51735727 | FRMD6 | copy fasta | chr14 | 51646910 | 51735727 |
a0001c0007t0001 | 0/0 | 4800 | 2 | 2 | 0 | 0 | 0 | 0 | FRMD6_chr14_51646910_51735727 | FRMD6 | copy fasta | chr14 | 51646910 | 51735727 |
a0001c0009t0001 | 0/0 | 4800 | 2 | 0 | 0 | 2 | 0 | 0 | FRMD6_chr14_51646910_51735727 | FRMD6 | copy fasta | chr14 | 51646910 | 51735727 |
a0001c0011t0001 | 0/0 | 4800 | 1 | 0 | 0 | 1 | 0 | 0 | FRMD6_chr14_51646910_51735727 | FRMD6 | copy fasta | chr14 | 51646910 | 51735727 |
a0001c0013t0001 | 0/0 | 4800 | 1 | 1 | 0 | 0 | 0 | 0 | FRMD6_chr14_51646910_51735727 | FRMD6 | copy fasta | chr14 | 51646910 | 51735727 |
a0001c0014t0001 | 0/0 | 4800 | 1 | 0 | 0 | 1 | 0 | 0 | FRMD6_chr14_51646910_51735727 | FRMD6 | copy fasta | chr14 | 51646910 | 51735727 |
a0001c0015t0001 | 0/0 | 4800 | 1 | 0 | 0 | 0 | 1 | 0 | FRMD6_chr14_51646910_51735727 | FRMD6 | copy fasta | chr14 | 51646910 | 51735727 |
a0002c0008t0009 | 0/0 | 4800 | 2 | 2 | 0 | 0 | 0 | 0 | FRMD6_chr14_51646910_51735727 | FRMD6 | copy fasta | chr14 | 51646910 | 51735727 |
a0003c0010t0001 | 0/0 | 4800 | 1 | 1 | 0 | 0 | 0 | 0 | FRMD6_chr14_51646910_51735727 | FRMD6 | copy fasta | chr14 | 51646910 | 51735727 |
a0004c0012t0002 | 0/0 | 4801 | 1 | 1 | 0 | 0 | 0 | 0 | FRMD6_chr14_51646910_51735727 | FRMD6 | copy fasta | chr14 | 51646910 | 51735727 |
a0005c0016t0002 | 0/0 | 4801 | 1 | 0 | 0 | 1 | 0 | 0 | FRMD6_chr14_51646910_51735727 | FRMD6 | copy fasta | chr14 | 51646910 | 51735727 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
a0001c0001t0001g0164 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
a0001c0001t0001g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
a0001c0001t0001g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
a0001c0001t0001g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
a0001c0001t0002g0001 | 0/0 | 6 | 0 | 0 | 5 | 0 | 1 | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
a0001c0001t0002g0002 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
a0001c0001t0002g0003 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
a0001c0001t0002g0008 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
a0001c0001t0002g0010 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
a0001c0001t0002g0012 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
a0001c0001t0002g0020 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
a0001c0001t0002g0023 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
a0001c0001t0002g0024 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
a0001c0001t0002g0026 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
a0001c0001t0002g0036 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
a0001c0001t0002g0037 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
a0001c0001t0002g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
a0001c0001t0002g0048 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
a0001c0001t0002g0049 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
a0001c0001t0002g0050 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
a0001c0001t0002g0051 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
a0001c0001t0002g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
a0001c0001t0002g0060 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
a0001c0001t0002g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
a0001c0001t0002g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
a0001c0001t0002g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
a0001c0001t0002g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
a0001c0001t0002g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
a0001c0001t0002g0102 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
a0001c0001t0002g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
a0001c0001t0002g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
a0001c0001t0002g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
a0001c0001t0002g0108 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
a0001c0001t0002g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
a0001c0001t0002g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
a0001c0001t0002g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
a0001c0001t0002g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
a0001c0001t0002g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
a0001c0001t0002g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
a0001c0001t0002g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
a0001c0001t0002g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
a0001c0001t0002g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
a0001c0001t0002g0120 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
a0001c0001t0002g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
a0001c0001t0002g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
a0001c0001t0002g0123 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
a0001c0001t0002g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
a0001c0001t0002g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
a0001c0001t0002g0133 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
a0001c0001t0002g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
a0001c0001t0002g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
a0001c0001t0002g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
a0001c0001t0002g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
a0001c0001t0002g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
a0001c0001t0002g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
a0001c0001t0002g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
a0001c0001t0002g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
a0001c0001t0002g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
a0001c0001t0002g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
a0001c0001t0002g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
a0001c0001t0002g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
a0001c0001t0002g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
a0001c0001t0002g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
a0001c0001t0002g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
a0001c0001t0002g0170 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
a0001c0001t0002g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
a0001c0001t0002g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
a0001c0001t0002g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
a0001c0001t0002g0192 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
a0001c0001t0002g0195 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
a0001c0001t0002g0203 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
a0001c0001t0002g0211 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
a0001c0001t0002g0230 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
a0001c0001t0002g0231 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
a0001c0001t0002g0253 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
a0001c0001t0002g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
a0001c0001t0002g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
a0001c0001t0002g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
a0001c0001t0002g0306 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
a0001c0001t0002g0311 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
a0001c0001t0002g0312 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
a0001c0001t0002g0315 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
a0001c0001t0006g0019 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
a0001c0001t0006g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
a0001c0001t0007g0095 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
a0001c0001t0007g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
a0001c0001t0007g0159 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
a0001c0001t0010g0002 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
a0001c0001t0010g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
a0001c0001t0011g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
a0001c0001t0011g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
a0001c0001t0018g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
a0001c0001t0019g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
a0001c0001t0020g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
a0001c0001t0021g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
a0001c0001t0023g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
a0001c0001t0024g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
a0001c0002t0001g0004 | 0/0 | 5 | 0 | 0 | 3 | 0 | 2 | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
a0001c0002t0001g0007 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
a0001c0002t0001g0013 | 0/0 | 3 | 0 | 2 | 0 | 1 | 0 | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
a0001c0002t0001g0025 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
a0001c0002t0001g0028 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
a0001c0002t0001g0030 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
a0001c0002t0001g0031 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
a0001c0002t0001g0032 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
a0001c0002t0001g0033 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
a0001c0002t0001g0039 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
a0001c0002t0001g0042 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
a0001c0002t0001g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
a0001c0002t0001g0074 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
a0001c0002t0001g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
a0001c0002t0001g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
a0001c0002t0001g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
a0001c0002t0001g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
a0001c0002t0001g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
a0001c0002t0001g0087 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
a0001c0002t0001g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
a0001c0002t0001g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
a0001c0002t0001g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
a0001c0002t0001g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
a0001c0002t0001g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
a0001c0002t0001g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
a0001c0002t0001g0097 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
a0001c0002t0001g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
a0001c0002t0001g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
a0001c0002t0001g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
a0001c0002t0001g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
a0001c0002t0001g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
a0001c0002t0001g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
a0001c0002t0001g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
a0001c0002t0001g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
a0001c0002t0001g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
a0001c0002t0001g0173 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
a0001c0002t0001g0174 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
a0001c0002t0001g0176 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
a0001c0002t0001g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
a0001c0002t0001g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
a0001c0002t0001g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
a0001c0002t0001g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
a0001c0002t0001g0184 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
a0001c0002t0001g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
a0001c0002t0001g0188 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
a0001c0002t0001g0189 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
a0001c0002t0001g0191 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
a0001c0002t0001g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
a0001c0002t0001g0196 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
a0001c0002t0001g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
a0001c0002t0001g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
a0001c0002t0001g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
a0001c0002t0001g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
a0001c0002t0001g0205 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
a0001c0002t0001g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
a0001c0002t0001g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
a0001c0002t0001g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
a0001c0002t0001g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
a0001c0002t0001g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
a0001c0002t0001g0219 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
a0001c0002t0001g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
a0001c0002t0001g0223 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
a0001c0002t0001g0225 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
a0001c0002t0001g0227 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
a0001c0002t0001g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
a0001c0002t0001g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
a0001c0002t0001g0234 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
a0001c0002t0001g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
a0001c0002t0001g0236 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
a0001c0002t0001g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
a0001c0002t0001g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
a0001c0002t0001g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
a0001c0002t0001g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
a0001c0002t0001g0245 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
a0001c0002t0001g0246 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
a0001c0002t0001g0265 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
a0001c0002t0001g0289 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
a0001c0002t0001g0290 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
a0001c0002t0001g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
a0001c0002t0001g0303 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
a0001c0002t0001g0304 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
a0001c0002t0002g0204 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
a0001c0002t0002g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
a0001c0002t0002g0226 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
a0001c0002t0004g0038 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
a0001c0002t0004g0222 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
a0001c0002t0004g0238 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
a0001c0002t0004g0247 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
a0001c0002t0008g0016 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
a0001c0002t0013g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
a0001c0002t0014g0243 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
a0001c0002t0015g0240 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
a0001c0002t0017g0213 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
a0001c0003t0001g0006 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
a0001c0003t0001g0011 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
a0001c0003t0001g0014 | 0/0 | 3 | 0 | 1 | 0 | 0 | 2 | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
a0001c0003t0001g0015 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
a0001c0003t0001g0017 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
a0001c0003t0001g0018 | 0/0 | 3 | 2 | 0 | 0 | 0 | 1 | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
a0001c0003t0001g0022 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
a0001c0003t0001g0029 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
a0001c0003t0001g0034 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
a0001c0003t0001g0040 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
a0001c0003t0001g0041 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
a0001c0003t0001g0043 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
a0001c0003t0001g0044 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
a0001c0003t0001g0045 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
a0001c0003t0001g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
a0001c0003t0001g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
a0001c0003t0001g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
a0001c0003t0001g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
a0001c0003t0001g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
a0001c0003t0001g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
a0001c0003t0001g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
a0001c0003t0001g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
a0001c0003t0001g0100 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
a0001c0003t0001g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
a0001c0003t0001g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
a0001c0003t0001g0175 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
a0001c0003t0001g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
a0001c0003t0001g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
a0001c0003t0001g0221 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
a0001c0003t0001g0228 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
a0001c0003t0001g0229 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
a0001c0003t0001g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
a0001c0003t0001g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
a0001c0003t0001g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
a0001c0003t0001g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
a0001c0003t0001g0254 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
a0001c0003t0001g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
a0001c0003t0001g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
a0001c0003t0001g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
a0001c0003t0001g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
a0001c0003t0001g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
a0001c0003t0001g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
a0001c0003t0001g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
a0001c0003t0001g0263 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
a0001c0003t0001g0264 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
a0001c0003t0001g0266 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
a0001c0003t0001g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
a0001c0003t0001g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
a0001c0003t0001g0269 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
a0001c0003t0001g0271 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
a0001c0003t0001g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
a0001c0003t0001g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
a0001c0003t0001g0274 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
a0001c0003t0001g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
a0001c0003t0001g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
a0001c0003t0001g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
a0001c0003t0001g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
a0001c0003t0001g0279 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
a0001c0003t0001g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
a0001c0003t0001g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
a0001c0003t0001g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
a0001c0003t0001g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
a0001c0003t0001g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
a0001c0003t0001g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
a0001c0003t0001g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
a0001c0003t0001g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
a0001c0003t0001g0299 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
a0001c0003t0001g0302 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
a0001c0003t0001g0305 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
a0001c0003t0001g0308 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
a0001c0003t0001g0309 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
a0001c0003t0001g0310 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
a0001c0003t0001g0313 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
a0001c0003t0001g0314 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
a0001c0003t0002g0270 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
a0001c0003t0002g0286 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
a0001c0004t0001g0035 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
a0001c0004t0001g0046 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
a0001c0004t0001g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
a0001c0004t0001g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
a0001c0004t0001g0064 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
a0001c0004t0001g0065 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
a0001c0004t0001g0066 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
a0001c0004t0001g0067 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
a0001c0004t0001g0068 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
a0001c0004t0001g0069 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
a0001c0004t0001g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
a0001c0004t0001g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
a0001c0004t0001g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
a0001c0004t0001g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
a0001c0004t0005g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
a0001c0004t0005g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
a0001c0004t0005g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
a0001c0004t0005g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
a0001c0004t0012g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
a0001c0004t0016g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
a0001c0005t0001g0005 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
a0001c0005t0001g0009 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
a0001c0005t0001g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
a0001c0005t0001g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
a0001c0005t0001g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
a0001c0005t0001g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
a0001c0005t0001g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
a0001c0005t0001g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
a0001c0005t0001g0307 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
a0001c0006t0003g0027 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
a0001c0006t0003g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
a0001c0006t0003g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
a0001c0006t0003g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
a0001c0006t0003g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
a0001c0006t0003g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
a0001c0006t0003g0167 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
a0001c0006t0003g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
a0001c0006t0022g0163 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
a0001c0007t0001g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
a0001c0007t0001g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
a0001c0009t0001g0021 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
a0001c0011t0001g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
a0001c0013t0001g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
a0001c0014t0001g0007 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
a0001c0015t0001g0242 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
a0002c0008t0009g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
a0002c0008t0009g0291 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
a0003c0010t0001g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
a0004c0012t0002g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
a0005c0016t0002g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0001 | c0002 | t0001 | g0176 | EUR | GBR | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
HG00099 | hp2 | a0001 | c0001 | t0002 | g0020 | EUR | GBR | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
HG00140 | hp1 | a0001 | c0003 | t0001 | g0314 | EUR | GBR | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
HG00140 | hp2 | a0001 | c0001 | t0002 | g0311 | EUR | GBR | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
HG00280 | hp1 | a0001 | c0004 | t0001 | g0067 | EUR | FIN | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
HG00280 | hp2 | a0001 | c0002 | t0004 | g0247 | EUR | FIN | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
HG00323 | hp1 | a0001 | c0003 | t0001 | g0313 | EUR | FIN | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
HG00323 | hp2 | a0001 | c0015 | t0001 | g0242 | EUR | FIN | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
HG00438 | hp1 | a0001 | c0003 | t0001 | g0277 | EAS | CHS | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
HG00438 | hp2 | a0001 | c0002 | t0001 | g0004 | EAS | CHS | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
HG00544 | hp1 | a0001 | c0001 | t0002 | g0082 | EAS | CHS | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
HG00544 | hp2 | a0001 | c0003 | t0001 | g0258 | EAS | CHS | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
HG00597 | hp1 | a0001 | c0001 | t0002 | g0080 | EAS | CHS | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
HG00597 | hp2 | a0001 | c0002 | t0001 | g0084 | EAS | CHS | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
HG00609 | hp1 | a0001 | c0002 | t0001 | g0136 | EAS | CHS | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
HG00609 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | CHS | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
HG00639 | hp1 | a0001 | c0004 | t0001 | g0046 | AMR | PUR | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
HG00639 | hp2 | a0001 | c0002 | t0001 | g0223 | AMR | PUR | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
HG00673 | hp1 | a0001 | c0001 | t0002 | g0155 | EAS | CHS | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
HG00673 | hp2 | a0001 | c0014 | t0001 | g0007 | EAS | CHS | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
HG00733 | hp1 | a0001 | c0002 | t0001 | g0234 | AMR | PUR | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
HG00733 | hp2 | a0001 | c0001 | t0007 | g0096 | AMR | PUR | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
HG00735 | hp1 | a0001 | c0002 | t0001 | g0087 | AMR | PUR | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
HG00735 | hp2 | a0001 | c0003 | t0001 | g0014 | AMR | PUR | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
HG00738 | hp1 | a0001 | c0001 | t0002 | g0048 | AMR | PUR | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
HG00738 | hp2 | a0001 | c0002 | t0001 | g0028 | AMR | PUR | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
HG00741 | hp1 | a0001 | c0002 | t0001 | g0028 | AMR | PUR | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
HG00741 | hp2 | a0001 | c0002 | t0001 | g0174 | AMR | PUR | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
HG01069 | hp1 | a0001 | c0003 | t0001 | g0266 | AMR | PUR | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
HG01069 | hp2 | a0001 | c0002 | t0004 | g0038 | AMR | PUR | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
HG01070 | hp1 | a0001 | c0002 | t0001 | g0246 | AMR | PUR | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
HG01070 | hp2 | a0001 | c0003 | t0001 | g0017 | AMR | PUR | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
HG01071 | hp1 | a0001 | c0003 | t0001 | g0017 | AMR | PUR | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
HG01071 | hp2 | a0001 | c0002 | t0004 | g0038 | AMR | PUR | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
HG01074 | hp1 | a0001 | c0002 | t0004 | g0238 | AMR | PUR | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
HG01074 | hp2 | a0001 | c0001 | t0002 | g0211 | AMR | PUR | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
HG01081 | hp1 | a0001 | c0003 | t0001 | g0043 | AMR | PUR | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
HG01081 | hp2 | a0001 | c0003 | t0001 | g0015 | AMR | PUR | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
HG01099 | hp1 | a0001 | c0002 | t0001 | g0290 | AMR | PUR | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
HG01099 | hp2 | a0001 | c0001 | t0002 | g0203 | AMR | PUR | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
HG01106 | hp1 | a0001 | c0002 | t0001 | g0173 | AMR | PUR | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
HG01106 | hp2 | a0001 | c0003 | t0001 | g0015 | AMR | PUR | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
HG01109 | hp1 | a0001 | c0004 | t0001 | g0064 | AMR | PUR | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
HG01109 | hp2 | a0001 | c0001 | t0007 | g0159 | AMR | PUR | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
HG01167 | hp1 | a0001 | c0003 | t0001 | g0263 | AMR | PUR | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
HG01167 | hp2 | a0001 | c0004 | t0001 | g0063 | AMR | PUR | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
HG01168 | hp1 | a0001 | c0003 | t0002 | g0270 | AMR | PUR | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
HG01168 | hp2 | a0001 | c0001 | t0002 | g0170 | AMR | PUR | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
HG01169 | hp1 | a0001 | c0003 | t0002 | g0286 | AMR | PUR | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
HG01169 | hp2 | a0001 | c0003 | t0001 | g0015 | AMR | PUR | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
HG01175 | hp1 | a0001 | c0003 | t0001 | g0264 | AMR | PUR | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
HG01175 | hp2 | a0001 | c0002 | t0001 | g0304 | AMR | PUR | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
HG01192 | hp1 | a0001 | c0003 | t0001 | g0221 | AMR | PUR | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
HG01192 | hp2 | a0001 | c0002 | t0004 | g0222 | AMR | PUR | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
HG01243 | hp1 | a0001 | c0002 | t0017 | g0213 | AMR | PUR | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
HG01243 | hp2 | a0001 | c0004 | t0001 | g0069 | AMR | PUR | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
HG01256 | hp1 | a0001 | c0001 | t0002 | g0051 | AMR | CLM | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
HG01256 | hp2 | a0001 | c0001 | t0002 | g0037 | AMR | CLM | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
HG01257 | hp1 | a0001 | c0002 | t0001 | g0031 | AMR | CLM | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
HG01257 | hp2 | a0001 | c0003 | t0001 | g0254 | AMR | CLM | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
HG01258 | hp1 | a0001 | c0002 | t0001 | g0031 | AMR | CLM | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
HG01258 | hp2 | a0001 | c0001 | t0002 | g0037 | AMR | CLM | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
HG01261 | hp1 | a0001 | c0001 | t0006 | g0019 | AMR | CLM | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
HG01261 | hp2 | a0001 | c0001 | t0007 | g0095 | AMR | CLM | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
HG01346 | hp1 | a0001 | c0002 | t0001 | g0032 | AMR | CLM | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
HG01346 | hp2 | a0001 | c0001 | t0002 | g0036 | AMR | CLM | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
HG01358 | hp1 | a0001 | c0006 | t0003 | g0167 | AMR | CLM | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
HG01358 | hp2 | a0001 | c0002 | t0002 | g0226 | AMR | CLM | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
HG01361 | hp1 | a0001 | c0002 | t0001 | g0013 | AMR | CLM | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
HG01361 | hp2 | a0001 | c0003 | t0001 | g0229 | AMR | CLM | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
HG01433 | hp1 | a0001 | c0006 | t0022 | g0163 | AMR | CLM | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
HG01433 | hp2 | a0001 | c0002 | t0001 | g0013 | AMR | CLM | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
HG01496 | hp1 | a0001 | c0002 | t0015 | g0240 | AMR | CLM | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
HG01496 | hp2 | a0001 | c0002 | t0001 | g0042 | AMR | CLM | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
HG01515 | hp1 | a0001 | c0003 | t0001 | g0269 | EUR | IBS | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
HG01515 | hp2 | a0001 | c0001 | t0002 | g0050 | EUR | IBS | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
HG01516 | hp1 | a0001 | c0001 | t0002 | g0020 | EUR | IBS | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
HG01516 | hp2 | a0001 | c0002 | t0001 | g0205 | EUR | IBS | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
HG01517 | hp1 | a0001 | c0001 | t0002 | g0049 | EUR | IBS | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
HG01517 | hp2 | a0001 | c0001 | t0002 | g0060 | EUR | IBS | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
HG01884 | hp1 | a0001 | c0002 | t0001 | g0206 | AFR | ACB | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
HG01884 | hp2 | a0001 | c0002 | t0001 | g0030 | AFR | ACB | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
HG01891 | hp1 | a0001 | c0001 | t0002 | g0114 | AFR | ACB | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
HG01891 | hp2 | a0001 | c0001 | t0002 | g0178 | AFR | ACB | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
HG01934 | hp1 | a0001 | c0003 | t0001 | g0017 | AMR | PEL | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
HG01934 | hp2 | a0001 | c0002 | t0001 | g0189 | AMR | PEL | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
HG01943 | hp1 | a0001 | c0001 | t0002 | g0230 | AMR | PEL | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
HG01943 | hp2 | a0001 | c0003 | t0001 | g0274 | AMR | PEL | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
HG01978 | hp1 | a0001 | c0002 | t0001 | g0303 | AMR | PEL | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
HG01978 | hp2 | a0001 | c0001 | t0002 | g0036 | AMR | PEL | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
HG01981 | hp1 | a0001 | c0002 | t0001 | g0219 | AMR | PEL | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
HG01981 | hp2 | a0001 | c0001 | t0002 | g0192 | AMR | PEL | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
HG02015 | hp1 | a0001 | c0003 | t0001 | g0268 | EAS | KHV | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
HG02015 | hp2 | a0001 | c0002 | t0001 | g0134 | EAS | KHV | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
HG02027 | hp1 | a0001 | c0003 | t0001 | g0302 | EAS | KHV | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
HG02027 | hp2 | a0001 | c0002 | t0001 | g0142 | EAS | KHV | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
HG02040 | hp1 | a0001 | c0002 | t0001 | g0127 | EAS | KHV | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
HG02040 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | KHV | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
HG02056 | hp1 | a0001 | c0002 | t0001 | g0007 | EAS | KHV | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
HG02056 | hp2 | a0001 | c0003 | t0001 | g0283 | EAS | KHV | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
HG02074 | hp1 | a0001 | c0005 | t0001 | g0251 | EAS | KHV | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
HG02074 | hp2 | a0001 | c0002 | t0001 | g0241 | EAS | KHV | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
HG02080 | hp1 | a0001 | c0001 | t0002 | g0024 | EAS | KHV | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
HG02080 | hp2 | a0001 | c0003 | t0001 | g0281 | EAS | KHV | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
HG02083 | hp1 | a0001 | c0003 | t0001 | g0287 | EAS | KHV | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
HG02083 | hp2 | a0001 | c0004 | t0005 | g0187 | EAS | KHV | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
HG02129 | hp1 | a0001 | c0003 | t0001 | g0275 | EAS | KHV | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
HG02129 | hp2 | a0001 | c0002 | t0001 | g0166 | EAS | KHV | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
HG02132 | hp1 | a0001 | c0001 | t0002 | g0023 | EAS | KHV | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
HG02132 | hp2 | a0001 | c0003 | t0001 | g0006 | EAS | KHV | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
HG02135 | hp1 | a0001 | c0001 | t0002 | g0121 | EAS | KHV | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
HG02135 | hp2 | a0001 | c0001 | t0002 | g0158 | EAS | KHV | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
HG02145 | hp1 | a0001 | c0002 | t0001 | g0177 | AFR | ACB | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
HG02145 | hp2 | a0001 | c0006 | t0003 | g0152 | AFR | ACB | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
HG02155 | hp1 | a0001 | c0003 | t0001 | g0044 | EAS | CDX | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
HG02155 | hp2 | a0001 | c0002 | t0001 | g0135 | EAS | CDX | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
HG02165 | hp1 | a0001 | c0001 | t0020 | g0130 | EAS | CDX | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
HG02165 | hp2 | a0001 | c0002 | t0001 | g0089 | EAS | CDX | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
HG02258 | hp1 | a0001 | c0003 | t0001 | g0018 | AFR | ACB | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
HG02258 | hp2 | a0002 | c0008 | t0009 | g0291 | AFR | ACB | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
HG02280 | hp1 | a0001 | c0001 | t0002 | g0146 | AFR | ACB | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
HG02280 | hp2 | a0001 | c0006 | t0003 | g0027 | AFR | ACB | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
HG02293 | hp1 | a0001 | c0002 | t0001 | g0184 | AMR | PEL | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
HG02293 | hp2 | a0001 | c0001 | t0002 | g0108 | AMR | PEL | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
HG02300 | hp1 | a0001 | c0002 | t0001 | g0188 | AMR | PEL | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
HG02300 | hp2 | a0001 | c0003 | t0001 | g0271 | AMR | PEL | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
HG02451 | hp1 | a0001 | c0001 | t0001 | g0209 | AFR | ACB | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
HG02451 | hp2 | a0001 | c0002 | t0001 | g0030 | AFR | ACB | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
HG02523 | hp1 | a0001 | c0001 | t0002 | g0122 | EAS | KHV | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
HG02523 | hp2 | a0001 | c0005 | t0001 | g0300 | EAS | KHV | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
HG02572 | hp1 | a0001 | c0001 | t0001 | g0202 | AFR | GWD | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
HG02572 | hp2 | a0002 | c0008 | t0009 | g0072 | AFR | GWD | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
HG02602 | hp1 | a0001 | c0001 | t0002 | g0001 | SAS | PJL | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
HG02602 | hp2 | a0001 | c0002 | t0001 | g0004 | SAS | PJL | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
HG02615 | hp1 | a0001 | c0002 | t0001 | g0197 | AFR | GWD | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
HG02615 | hp2 | a0001 | c0003 | t0001 | g0212 | AFR | GWD | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
HG02630 | hp1 | a0001 | c0007 | t0001 | g0053 | AFR | GWD | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
HG02630 | hp2 | a0001 | c0002 | t0001 | g0180 | AFR | GWD | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
HG02698 | hp1 | a0001 | c0002 | t0001 | g0032 | SAS | PJL | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
HG02698 | hp2 | a0001 | c0004 | t0001 | g0066 | SAS | PJL | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
HG02717 | hp1 | a0001 | c0001 | t0002 | g0169 | AFR | GWD | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
HG02717 | hp2 | a0001 | c0002 | t0001 | g0214 | AFR | GWD | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
HG02723 | hp1 | a0001 | c0013 | t0001 | g0201 | AFR | GWD | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
HG02723 | hp2 | a0001 | c0004 | t0001 | g0141 | AFR | GWD | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
HG02735 | hp1 | a0001 | c0002 | t0001 | g0236 | SAS | PJL | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
HG02735 | hp2 | a0001 | c0001 | t0002 | g0133 | SAS | PJL | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
HG02809 | hp1 | a0001 | c0001 | t0002 | g0012 | AFR | GWD | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
HG02809 | hp2 | a0001 | c0002 | t0001 | g0200 | AFR | GWD | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
HG02818 | hp1 | a0001 | c0003 | t0001 | g0011 | AFR | GWD | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
HG02818 | hp2 | a0001 | c0004 | t0016 | g0070 | AFR | GWD | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
HG02886 | hp1 | a0001 | c0003 | t0001 | g0011 | AFR | GWD | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
HG02886 | hp2 | a0001 | c0001 | t0002 | g0148 | AFR | GWD | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
HG02895 | hp1 | a0001 | c0001 | t0002 | g0054 | AFR | GWD | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
HG02895 | hp2 | a0001 | c0004 | t0001 | g0035 | AFR | GWD | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
HG02896 | hp1 | a0001 | c0001 | t0002 | g0172 | AFR | GWD | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
HG02896 | hp2 | a0001 | c0001 | t0011 | g0131 | AFR | GWD | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
HG02897 | hp1 | a0001 | c0004 | t0001 | g0035 | AFR | GWD | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
HG02897 | hp2 | a0001 | c0001 | t0011 | g0132 | AFR | GWD | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
HG02922 | hp1 | a0001 | c0001 | t0021 | g0218 | AFR | ESN | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
HG02922 | hp2 | a0001 | c0002 | t0013 | g0052 | AFR | ESN | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
HG02965 | hp1 | a0001 | c0002 | t0001 | g0181 | AFR | ESN | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
HG02965 | hp2 | a0001 | c0001 | t0006 | g0059 | AFR | ESN | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
HG02970 | hp1 | a0001 | c0003 | t0001 | g0055 | AFR | ESN | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
HG02970 | hp2 | a0001 | c0006 | t0003 | g0073 | AFR | ESN | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
HG02976 | hp1 | a0001 | c0006 | t0003 | g0151 | AFR | ESN | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
HG02976 | hp2 | a0001 | c0002 | t0001 | g0289 | AFR | ESN | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
HG03041 | hp1 | a0001 | c0003 | t0001 | g0034 | AFR | GWD | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
HG03041 | hp2 | a0001 | c0001 | t0002 | g0012 | AFR | GWD | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
HG03098 | hp1 | a0001 | c0004 | t0001 | g0140 | AFR | MSL | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
HG03098 | hp2 | a0001 | c0006 | t0003 | g0154 | AFR | MSL | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
HG03130 | hp1 | a0001 | c0001 | t0002 | g0012 | AFR | ESN | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
HG03130 | hp2 | a0001 | c0003 | t0001 | g0034 | AFR | ESN | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
HG03139 | hp1 | a0003 | c0010 | t0001 | g0071 | AFR | ESN | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
HG03139 | hp2 | a0001 | c0002 | t0001 | g0216 | AFR | ESN | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
HG03195 | hp1 | a0001 | c0004 | t0001 | g0208 | AFR | ESN | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
HG03195 | hp2 | a0001 | c0006 | t0003 | g0153 | AFR | ESN | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
HG03209 | hp1 | a0001 | c0004 | t0012 | g0182 | AFR | MSL | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
HG03209 | hp2 | a0001 | c0003 | t0001 | g0011 | AFR | MSL | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
HG03225 | hp1 | a0001 | c0002 | t0001 | g0150 | AFR | MSL | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
HG03225 | hp2 | a0001 | c0001 | t0002 | g0115 | AFR | MSL | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
HG03239 | hp1 | a0001 | c0004 | t0001 | g0068 | SAS | PJL | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
HG03239 | hp2 | a0001 | c0003 | t0001 | g0045 | SAS | PJL | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
HG03453 | hp1 | a0001 | c0003 | t0001 | g0098 | AFR | MSL | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
HG03453 | hp2 | a0001 | c0002 | t0001 | g0042 | AFR | MSL | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
HG03486 | hp1 | a0001 | c0006 | t0003 | g0183 | AFR | MSL | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
HG03486 | hp2 | a0001 | c0001 | t0024 | g0124 | AFR | MSL | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
HG03490 | hp1 | a0001 | c0001 | t0002 | g0123 | SAS | PJL | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
HG03490 | hp2 | a0001 | c0003 | t0001 | g0014 | SAS | PJL | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
HG03491 | hp1 | a0001 | c0002 | t0014 | g0243 | SAS | PJL | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
HG03491 | hp2 | a0001 | c0002 | t0001 | g0033 | SAS | PJL | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
HG03492 | hp1 | a0001 | c0003 | t0001 | g0014 | SAS | PJL | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
HG03492 | hp2 | a0001 | c0002 | t0001 | g0033 | SAS | PJL | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
HG03516 | hp1 | a0001 | c0002 | t0001 | g0217 | AFR | ESN | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
HG03516 | hp2 | a0001 | c0006 | t0003 | g0027 | AFR | ESN | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
HG03540 | hp1 | a0001 | c0002 | t0001 | g0057 | AFR | GWD | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
HG03540 | hp2 | a0001 | c0007 | t0001 | g0101 | AFR | GWD | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
HG03579 | hp1 | a0001 | c0004 | t0001 | g0056 | AFR | MSL | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
HG03579 | hp2 | a0001 | c0002 | t0001 | g0199 | AFR | MSL | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
HG03688 | hp1 | a0001 | c0002 | t0001 | g0074 | SAS | STU | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
HG03688 | hp2 | a0001 | c0001 | t0001 | g0164 | SAS | STU | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
HG03710 | hp1 | a0001 | c0003 | t0001 | g0045 | SAS | PJL | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
HG03710 | hp2 | a0001 | c0002 | t0001 | g0227 | SAS | PJL | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
HG03831 | hp1 | a0001 | c0002 | t0001 | g0225 | SAS | BEB | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
HG03831 | hp2 | a0001 | c0003 | t0001 | g0100 | SAS | BEB | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
HG03834 | hp1 | a0001 | c0004 | t0001 | g0065 | SAS | BEB | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
HG03834 | hp2 | a0001 | c0002 | t0001 | g0004 | SAS | BEB | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
HG03927 | hp1 | a0001 | c0002 | t0001 | g0196 | SAS | BEB | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
HG03927 | hp2 | a0001 | c0001 | t0002 | g0120 | SAS | BEB | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
HG03942 | hp1 | a0001 | c0001 | t0002 | g0195 | SAS | BEB | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
HG03942 | hp2 | a0001 | c0002 | t0002 | g0204 | SAS | BEB | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
HG04184 | hp1 | a0001 | c0003 | t0001 | g0310 | SAS | BEB | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
HG04184 | hp2 | a0001 | c0001 | t0002 | g0102 | SAS | BEB | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
HG04199 | hp1 | a0001 | c0001 | t0002 | g0231 | SAS | STU | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
HG04199 | hp2 | a0001 | c0002 | t0001 | g0265 | SAS | STU | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
HG04228 | hp1 | a0001 | c0002 | t0001 | g0245 | SAS | STU | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
HG04228 | hp2 | a0001 | c0003 | t0001 | g0018 | SAS | STU | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
NA18522 | hp1 | a0001 | c0003 | t0001 | g0099 | AFR | YRI | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
NA18522 | hp2 | a0001 | c0001 | t0002 | g0147 | AFR | YRI | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
NA18612 | hp1 | a0001 | c0003 | t0001 | g0079 | EAS | CHB | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
NA18612 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | CHB | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
NA18747 | hp1 | a0001 | c0002 | t0001 | g0090 | EAS | CHB | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
NA18747 | hp2 | a0001 | c0003 | t0001 | g0044 | EAS | CHB | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
NA18906 | hp1 | a0001 | c0001 | t0019 | g0103 | AFR | YRI | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
NA18906 | hp2 | a0001 | c0002 | t0001 | g0198 | AFR | YRI | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
NA18939 | hp1 | a0001 | c0003 | t0001 | g0006 | EAS | JPT | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
NA18939 | hp2 | a0001 | c0002 | t0001 | g0232 | EAS | JPT | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
NA18941 | hp1 | a0001 | c0003 | t0001 | g0299 | EAS | JPT | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
NA18941 | hp2 | a0001 | c0002 | t0001 | g0220 | EAS | JPT | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
NA18942 | hp1 | a0001 | c0003 | t0001 | g0006 | EAS | JPT | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
NA18942 | hp2 | a0001 | c0001 | t0002 | g0162 | EAS | JPT | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
NA18944 | hp1 | a0001 | c0005 | t0001 | g0009 | EAS | JPT | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
NA18944 | hp2 | a0001 | c0001 | t0002 | g0010 | EAS | JPT | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
NA18945 | hp1 | a0001 | c0002 | t0001 | g0025 | EAS | JPT | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
NA18945 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
NA18946 | hp1 | a0001 | c0001 | t0002 | g0295 | EAS | JPT | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
NA18946 | hp2 | a0001 | c0009 | t0001 | g0021 | EAS | JPT | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
NA18947 | hp1 | a0001 | c0001 | t0002 | g0294 | EAS | JPT | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
NA18947 | hp2 | a0001 | c0002 | t0001 | g0004 | EAS | JPT | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
NA18949 | hp1 | a0001 | c0001 | t0002 | g0104 | EAS | JPT | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
NA18949 | hp2 | a0001 | c0003 | t0001 | g0252 | EAS | JPT | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
NA18950 | hp1 | a0001 | c0005 | t0001 | g0301 | EAS | JPT | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
NA18950 | hp2 | a0001 | c0001 | t0002 | g0008 | EAS | JPT | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
NA18951 | hp1 | a0001 | c0002 | t0001 | g0083 | EAS | JPT | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
NA18951 | hp2 | a0001 | c0001 | t0002 | g0062 | EAS | JPT | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
NA18952 | hp1 | a0001 | c0005 | t0001 | g0005 | EAS | JPT | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
NA18952 | hp2 | a0001 | c0001 | t0002 | g0107 | EAS | JPT | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
NA18953 | hp1 | a0001 | c0003 | t0001 | g0261 | EAS | JPT | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
NA18953 | hp2 | a0001 | c0002 | t0001 | g0025 | EAS | JPT | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
NA18954 | hp1 | a0001 | c0002 | t0001 | g0244 | EAS | JPT | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
NA18954 | hp2 | a0001 | c0001 | t0002 | g0118 | EAS | JPT | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
NA18957 | hp1 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
NA18957 | hp2 | a0001 | c0002 | t0008 | g0016 | EAS | JPT | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
NA18960 | hp1 | a0001 | c0002 | t0001 | g0233 | EAS | JPT | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
NA18960 | hp2 | a0001 | c0001 | t0002 | g0285 | EAS | JPT | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
NA18961 | hp1 | a0001 | c0001 | t0002 | g0109 | EAS | JPT | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
NA18961 | hp2 | a0001 | c0002 | t0008 | g0016 | EAS | JPT | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
NA18962 | hp1 | a0001 | c0003 | t0001 | g0257 | EAS | JPT | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
NA18962 | hp2 | a0001 | c0001 | t0010 | g0111 | EAS | JPT | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
NA18964 | hp1 | a0001 | c0003 | t0001 | g0029 | EAS | JPT | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
NA18964 | hp2 | a0001 | c0005 | t0001 | g0297 | EAS | JPT | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
NA18965 | hp1 | a0001 | c0001 | t0002 | g0081 | EAS | JPT | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
NA18965 | hp2 | a0001 | c0002 | t0001 | g0007 | EAS | JPT | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
NA18966 | hp1 | a0001 | c0001 | t0002 | g0156 | EAS | JPT | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
NA18966 | hp2 | a0001 | c0001 | t0002 | g0008 | EAS | JPT | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
NA18967 | hp1 | a0001 | c0001 | t0002 | g0157 | EAS | JPT | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
NA18967 | hp2 | a0001 | c0003 | t0001 | g0282 | EAS | JPT | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
NA18968 | hp1 | a0001 | c0011 | t0001 | g0256 | EAS | JPT | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
NA18968 | hp2 | a0001 | c0005 | t0001 | g0005 | EAS | JPT | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
NA18969 | hp1 | a0001 | c0005 | t0001 | g0009 | EAS | JPT | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
NA18969 | hp2 | a0001 | c0003 | t0001 | g0165 | EAS | JPT | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
NA18970 | hp1 | a0001 | c0001 | t0002 | g0105 | EAS | JPT | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
NA18970 | hp2 | a0001 | c0003 | t0001 | g0041 | EAS | JPT | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
NA18971 | hp1 | a0001 | c0005 | t0001 | g0126 | EAS | JPT | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
NA18971 | hp2 | a0001 | c0002 | t0001 | g0296 | EAS | JPT | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
NA18972 | hp1 | a0001 | c0002 | t0001 | g0092 | EAS | JPT | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
NA18972 | hp2 | a0001 | c0003 | t0001 | g0077 | EAS | JPT | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
NA18973 | hp1 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
NA18973 | hp2 | a0001 | c0003 | t0001 | g0022 | EAS | JPT | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
NA18974 | hp1 | a0001 | c0003 | t0001 | g0248 | EAS | JPT | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
NA18974 | hp2 | a0001 | c0001 | t0002 | g0010 | EAS | JPT | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
NA18977 | hp1 | a0001 | c0001 | t0002 | g0160 | EAS | JPT | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
NA18977 | hp2 | a0001 | c0003 | t0001 | g0255 | EAS | JPT | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
NA18978 | hp1 | a0001 | c0003 | t0001 | g0250 | EAS | JPT | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
NA18978 | hp2 | a0001 | c0001 | t0002 | g0161 | EAS | JPT | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
NA18979 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
NA18979 | hp2 | a0001 | c0003 | t0001 | g0094 | EAS | JPT | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
NA18981 | hp1 | a0001 | c0003 | t0001 | g0308 | EAS | JPT | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
NA18981 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
NA18983 | hp1 | a0001 | c0005 | t0001 | g0005 | EAS | JPT | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
NA18983 | hp2 | a0001 | c0002 | t0001 | g0004 | EAS | JPT | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
NA18984 | hp1 | a0001 | c0003 | t0001 | g0029 | EAS | JPT | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
NA18984 | hp2 | a0001 | c0001 | t0002 | g0026 | EAS | JPT | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
NA18986 | hp1 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
NA18986 | hp2 | a0001 | c0002 | t0001 | g0088 | EAS | JPT | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
NA18988 | hp1 | a0001 | c0003 | t0001 | g0278 | EAS | JPT | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
NA18988 | hp2 | a0001 | c0001 | t0002 | g0128 | EAS | JPT | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
NA18990 | hp1 | a0001 | c0002 | t0001 | g0086 | EAS | JPT | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
NA18990 | hp2 | a0001 | c0003 | t0001 | g0259 | EAS | JPT | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
NA18991 | hp1 | a0001 | c0003 | t0001 | g0076 | EAS | JPT | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
NA18991 | hp2 | a0001 | c0001 | t0002 | g0061 | EAS | JPT | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
NA18993 | hp1 | a0001 | c0001 | t0002 | g0116 | EAS | JPT | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
NA18993 | hp2 | a0001 | c0003 | t0001 | g0249 | EAS | JPT | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
NA18994 | hp1 | a0001 | c0003 | t0001 | g0284 | EAS | JPT | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
NA18994 | hp2 | a0001 | c0004 | t0005 | g0185 | EAS | JPT | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
NA18995 | hp1 | a0001 | c0001 | t0002 | g0024 | EAS | JPT | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
NA18995 | hp2 | a0001 | c0002 | t0001 | g0075 | EAS | JPT | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
NA18998 | hp1 | a0001 | c0003 | t0001 | g0305 | EAS | JPT | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
NA18998 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
NA18999 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
NA18999 | hp2 | a0001 | c0003 | t0001 | g0043 | EAS | JPT | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
NA19000 | hp1 | a0001 | c0001 | t0002 | g0023 | EAS | JPT | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
NA19000 | hp2 | a0001 | c0003 | t0001 | g0280 | EAS | JPT | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
NA19001 | hp1 | a0001 | c0002 | t0001 | g0093 | EAS | JPT | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
NA19001 | hp2 | a0001 | c0001 | t0002 | g0119 | EAS | JPT | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
NA19002 | hp1 | a0001 | c0003 | t0001 | g0040 | EAS | JPT | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
NA19002 | hp2 | a0001 | c0001 | t0002 | g0008 | EAS | JPT | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
NA19003 | hp1 | a0001 | c0005 | t0001 | g0005 | EAS | JPT | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
NA19003 | hp2 | a0001 | c0001 | t0002 | g0117 | EAS | JPT | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
NA19005 | hp1 | a0001 | c0001 | t0002 | g0010 | EAS | JPT | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
NA19005 | hp2 | a0001 | c0005 | t0001 | g0009 | EAS | JPT | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
NA19006 | hp1 | a0001 | c0003 | t0001 | g0272 | EAS | JPT | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
NA19006 | hp2 | a0001 | c0001 | t0002 | g0112 | EAS | JPT | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
NA19007 | hp1 | a0001 | c0002 | t0001 | g0039 | EAS | JPT | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
NA19007 | hp2 | a0001 | c0003 | t0001 | g0022 | EAS | JPT | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
NA19009 | hp1 | a0001 | c0001 | t0010 | g0002 | EAS | JPT | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
NA19009 | hp2 | a0001 | c0003 | t0001 | g0293 | EAS | JPT | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
NA19010 | hp1 | a0001 | c0001 | t0002 | g0110 | EAS | JPT | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
NA19010 | hp2 | a0001 | c0009 | t0001 | g0021 | EAS | JPT | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
NA19011 | hp1 | a0001 | c0003 | t0001 | g0288 | EAS | JPT | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
NA19011 | hp2 | a0001 | c0002 | t0001 | g0237 | EAS | JPT | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
NA19012 | hp1 | a0001 | c0003 | t0001 | g0273 | EAS | JPT | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
NA19012 | hp2 | a0001 | c0002 | t0001 | g0125 | EAS | JPT | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
NA19030 | hp1 | a0001 | c0004 | t0001 | g0207 | AFR | LWK | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
NA19030 | hp2 | a0001 | c0003 | t0001 | g0194 | AFR | LWK | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
NA19054 | hp1 | a0001 | c0001 | t0002 | g0306 | EAS | JPT | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
NA19054 | hp2 | a0001 | c0002 | t0001 | g0239 | EAS | JPT | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
NA19055 | hp1 | a0001 | c0004 | t0005 | g0292 | EAS | JPT | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
NA19055 | hp2 | a0001 | c0002 | t0001 | g0186 | EAS | JPT | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
NA19058 | hp1 | a0001 | c0002 | t0001 | g0085 | EAS | JPT | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
NA19058 | hp2 | a0001 | c0003 | t0001 | g0262 | EAS | JPT | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
NA19063 | hp1 | a0001 | c0001 | t0002 | g0129 | EAS | JPT | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
NA19063 | hp2 | a0001 | c0002 | t0008 | g0016 | EAS | JPT | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
NA19066 | hp1 | a0005 | c0016 | t0002 | g0106 | EAS | JPT | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
NA19066 | hp2 | a0001 | c0003 | t0001 | g0138 | EAS | JPT | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
NA19067 | hp1 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
NA19067 | hp2 | a0001 | c0003 | t0001 | g0276 | EAS | JPT | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
NA19072 | hp1 | a0001 | c0002 | t0001 | g0039 | EAS | JPT | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
NA19072 | hp2 | a0001 | c0001 | t0002 | g0315 | EAS | JPT | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
NA19074 | hp1 | a0001 | c0003 | t0001 | g0006 | EAS | JPT | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
NA19074 | hp2 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
NA19077 | hp1 | a0001 | c0002 | t0001 | g0235 | EAS | JPT | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
NA19077 | hp2 | a0001 | c0003 | t0001 | g0309 | EAS | JPT | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
NA19078 | hp1 | a0001 | c0003 | t0001 | g0078 | EAS | JPT | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
NA19078 | hp2 | a0001 | c0002 | t0001 | g0091 | EAS | JPT | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
NA19079 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
NA19079 | hp2 | a0001 | c0003 | t0001 | g0267 | EAS | JPT | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
NA19081 | hp1 | a0001 | c0003 | t0001 | g0260 | EAS | JPT | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
NA19081 | hp2 | a0001 | c0005 | t0001 | g0298 | EAS | JPT | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
NA19082 | hp1 | a0001 | c0002 | t0002 | g0224 | EAS | JPT | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
NA19082 | hp2 | a0001 | c0004 | t0005 | g0190 | EAS | JPT | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
NA19085 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
NA19085 | hp2 | a0001 | c0003 | t0001 | g0040 | EAS | JPT | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
NA19087 | hp1 | a0001 | c0005 | t0001 | g0307 | EAS | JPT | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
NA19087 | hp2 | a0001 | c0001 | t0001 | g0168 | EAS | JPT | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
NA19090 | hp1 | a0001 | c0001 | t0002 | g0026 | EAS | JPT | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
NA19090 | hp2 | a0001 | c0003 | t0001 | g0041 | EAS | JPT | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
NA19240 | hp1 | a0004 | c0012 | t0002 | g0210 | AFR | YRI | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
NA19240 | hp2 | a0001 | c0001 | t0006 | g0019 | AFR | YRI | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
NA20129 | hp1 | a0001 | c0003 | t0001 | g0018 | AFR | ASW | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
NA20129 | hp2 | a0001 | c0001 | t0002 | g0139 | AFR | ASW | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
NA20805 | hp1 | a0001 | c0002 | t0001 | g0013 | EUR | TSI | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
NA20805 | hp2 | a0001 | c0003 | t0001 | g0175 | EUR | TSI | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
HG01123 | hp1 | a0001 | c0003 | t0001 | g0228 | AMR | CLM | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
HG01123 | hp2 | a0001 | c0002 | t0001 | g0191 | AMR | CLM | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
HG02109 | hp1 | a0001 | c0001 | t0002 | g0144 | AFR | ACB | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
HG02109 | hp2 | a0001 | c0001 | t0002 | g0312 | AFR | ACB | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
HG02486 | hp1 | a0001 | c0001 | t0001 | g0113 | AFR | ACB | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
HG02486 | hp2 | a0001 | c0001 | t0002 | g0149 | AFR | ACB | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
HG02559 | hp1 | a0001 | c0001 | t0018 | g0145 | AFR | ACB | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
HG02559 | hp2 | a0001 | c0002 | t0001 | g0215 | AFR | ACB | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
HG03471 | hp1 | a0001 | c0001 | t0023 | g0058 | AFR | MSL | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
HG03471 | hp2 | a0001 | c0002 | t0001 | g0179 | AFR | MSL | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
HG06807 | hp1 | a0001 | c0001 | t0002 | g0171 | AFR | USA | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
HG06807 | hp2 | a0001 | c0002 | t0001 | g0193 | AFR | USA | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
NA20300 | hp1 | a0001 | c0002 | t0001 | g0137 | AFR | USA | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
NA20300 | hp2 | a0001 | c0001 | t0002 | g0047 | AFR | USA | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
NA21309 | hp1 | a0001 | c0001 | t0002 | g0143 | AFR | LWK | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
NA21309 | hp2 | a0001 | c0001 | t0002 | g0253 | AFR | LWK | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
homoSapiens_chm13v2 | hp1 | a0001 | c0003 | t0001 | g0279 | REF | REF | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
homoSapiens_grch38 | hp1 | a0001 | c0002 | t0001 | g0097 | REF | REF | FRMD6_chr14_51646910_51735727 | FRMD6 | chr14 | 51646910 | 51735727 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr14:51689860
|
C | A | 1 | a0003 | 1 | HG03139.hp1 | missense_variant | MODERATE | c.24C>A | p.Asn8Lys | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 2/14 | 257/4800 | 24/1869 | 8/622 | chr14 | 51689860 | ||
chr14:51689930
|
A | G | 1 | a0005 | 1 | NA19066.hp1 | missense_variant | MODERATE | c.94A>G | p.Ile32Val | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 2/14 | 327/4800 | 94/1869 | 32/622 | chr14 | 51689930 | ||
chr14:51720216
|
G | A | 1 | a0004 | 1 | NA19240.hp1 | missense_variant | MODERATE | c.1186G>A | p.Gly396Ser | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 11/14 | 1419/4800 | 1186/1869 | 396/622 | chr14 | 51720216 | ||
chr14:51727853
|
A | T | 1 | a0002 | 2 | HG02258.hp2 HG02572.hp2 |
missense_variant | MODERATE | c.1693A>T | p.Thr565Ser | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 14/14 | 1926/4800 | 1693/1869 | 565/622 | chr14 | 51727853 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr14:51698198
|
G | A | 1 | a0001c0007 | 2 | HG02630.hp1 HG03540.hp2 |
synonymous_variant | LOW | c.156G>A | p.Lys52Lys | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 3/14 | 389/4800 | 156/1869 | 52/622 | chr14 | 51698198 | ||
chr14:51708158
|
C | T | 1 | a0001c0005 | 14 | HG02074.hp1 HG02523.hp2 NA18944.hp1 others(11): Show |
synonymous_variant | LOW | c.639C>T | p.Ser213Ser | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 7/14 | 872/4800 | 639/1869 | 213/622 | chr14 | 51708158 | ||
chr14:51715363
|
T | A | 11 | a0001c0001a0001c0003a0001c0004others(8): Show | 261 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(258): Show |
synonymous_variant | LOW | c.888T>A | p.Ser296Ser | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 10/14 | 1121/4800 | 888/1869 | 296/622 | chr14 | 51715363 | ||
chr14:51715390
|
G | A | 1 | a0001c0011 | 1 | NA18968.hp1 | synonymous_variant | LOW | c.915G>A | p.Gly305Gly | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 10/14 | 1148/4800 | 915/1869 | 305/622 | chr14 | 51715390 | ||
chr14:51720077
|
T | C | 1 | a0001c0006 | 10 | HG01358.hp1 HG01433.hp1 HG02145.hp2 others(7): Show |
synonymous_variant | LOW | c.1047T>C | p.Ser349Ser | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 11/14 | 1280/4800 | 1047/1869 | 349/622 | chr14 | 51720077 | ||
chr14:51720092
|
C | T | 1 | a0001c0013 | 1 | HG02723.hp1 | synonymous_variant | LOW | c.1062C>T | p.Asn354Asn | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 11/14 | 1295/4800 | 1062/1869 | 354/622 | chr14 | 51720092 | ||
chr14:51720248
|
G | A | 5 | a0001c0003a0001c0007a0001c0009others(2): Show | 103 | HG00140.hp1 HG00323.hp1 HG00438.hp1 others(100): Show |
synonymous_variant | LOW | c.1218G>A | p.Thr406Thr | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 11/14 | 1451/4800 | 1218/1869 | 406/622 | chr14 | 51720248 | ||
chr14:51720254
|
A | G | 4 | a0001c0001a0001c0015a0004c0012others(1): Show | 127 | HG00099.hp2 HG00140.hp2 HG00323.hp2 others(124): Show |
synonymous_variant | LOW | c.1224A>G | p.Pro408Pro | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 11/14 | 1457/4800 | 1224/1869 | 408/622 | chr14 | 51720254 | ||
chr14:51720323
|
C | T | 1 | a0001c0014 | 1 | HG00673.hp2 | synonymous_variant | LOW | c.1293C>T | p.Gly431Gly | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 11/14 | 1526/4800 | 1293/1869 | 431/622 | chr14 | 51720323 | ||
chr14:51722052
|
C | T | 1 | a0002c0008 | 2 | HG02258.hp2 HG02572.hp2 |
synonymous_variant | LOW | c.1464C>T | p.Leu488Leu | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 12/14 | 1697/4800 | 1464/1869 | 488/622 | chr14 | 51722052 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr14:51651917
|
G | A | 1 | a0001c0002t0004 | 5 | HG00280.hp2 HG01069.hp2 HG01071.hp2 others(2): Show |
5_prime_UTR_variant | MODIFIER | c.-226G>A | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 1/14 | 37920 | chr14 | 51651917 | |||||
chr14:51651935
|
G | T | 1 | a0001c0001t0011 | 2 | HG02896.hp2 HG02897.hp2 |
5_prime_UTR_variant | MODIFIER | c.-208G>T | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 1/14 | 37902 | chr14 | 51651935 | |||||
chr14:51728037
|
C | G | 1 | a0001c0001t0024 | 1 | HG03486.hp2 | 3_prime_UTR_variant | MODIFIER | c.*8C>G | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 14/14 | 8 | chr14 | 51728037 | |||||
chr14:51728080
|
C | T | 1 | a0001c0001t0023 | 1 | HG03471.hp1 | 3_prime_UTR_variant | MODIFIER | c.*51C>T | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 14/14 | 51 | chr14 | 51728080 | |||||
chr14:51728115
|
A | G | 1 | a0001c0002t0008 | 3 | NA18957.hp2 NA18961.hp2 NA19063.hp2 |
3_prime_UTR_variant | MODIFIER | c.*86A>G | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 14/14 | 86 | chr14 | 51728115 | |||||
chr14:51728232
|
G | T | 2 | a0001c0006t0003a0001c0006t0022 | 10 | HG01358.hp1 HG01433.hp1 HG02145.hp2 others(7): Show |
3_prime_UTR_variant | MODIFIER | c.*203G>T | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 14/14 | 203 | chr14 | 51728232 | |||||
chr14:51728371
|
A | AT | 15 | a0001c0001t0002a0001c0001t0006a0001c0001t0007others(12): Show | 126 | HG00099.hp2 HG00140.hp2 HG00544.hp1 others(123): Show |
3_prime_UTR_variant | MODIFIER | c.*349dupT | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 14/14 | 350 | INFO_REALIGN_3_PRIME | chr14 | 51728371 | ||||
chr14:51728572
|
G | A | 16 | a0001c0001t0002a0001c0001t0006a0001c0001t0007others(13): Show | 127 | HG00099.hp2 HG00140.hp2 HG00544.hp1 others(124): Show |
3_prime_UTR_variant | MODIFIER | c.*543G>A | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 14/14 | 543 | chr14 | 51728572 | |||||
chr14:51728602
|
A | G | 16 | a0001c0001t0002a0001c0001t0006a0001c0001t0007others(13): Show | 127 | HG00099.hp2 HG00140.hp2 HG00544.hp1 others(124): Show |
3_prime_UTR_variant | MODIFIER | c.*573A>G | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 14/14 | 573 | chr14 | 51728602 | |||||
chr14:51728827
|
C | T | 1 | a0001c0002t0017 | 1 | HG01243.hp1 | 3_prime_UTR_variant | MODIFIER | c.*798C>T | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 14/14 | 798 | chr14 | 51728827 | |||||
chr14:51728915
|
A | G | 1 | a0002c0008t0009 | 2 | HG02258.hp2 HG02572.hp2 |
3_prime_UTR_variant | MODIFIER | c.*886A>G | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 14/14 | 886 | chr14 | 51728915 | |||||
chr14:51729138
|
T | C | 1 | a0001c0001t0018 | 1 | HG02559.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1109T>C | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 14/14 | 1109 | chr14 | 51729138 | |||||
chr14:51729397
|
A | G | 1 | a0001c0001t0007 | 3 | HG00733.hp2 HG01109.hp2 HG01261.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1368A>G | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 14/14 | 1368 | chr14 | 51729397 | |||||
chr14:51729450
|
A | C | 1 | a0001c0001t0021 | 1 | HG02922.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1421A>C | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 14/14 | 1421 | chr14 | 51729450 | |||||
chr14:51729565
|
C | T | 1 | a0001c0004t0016 | 1 | HG02818.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1536C>T | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 14/14 | 1536 | chr14 | 51729565 | |||||
chr14:51729599
|
A | C | 1 | a0001c0004t0005 | 4 | HG02083.hp2 NA18994.hp2 NA19055.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*1570A>C | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 14/14 | 1570 | chr14 | 51729599 | |||||
chr14:51729616
|
A | G | 1 | a0001c0006t0022 | 1 | HG01433.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1587A>G | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 14/14 | 1587 | chr14 | 51729616 | |||||
chr14:51729780
|
C | T | 1 | a0001c0001t0024 | 1 | HG03486.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1751C>T | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 14/14 | 1751 | chr14 | 51729780 | |||||
chr14:51729787
|
G | A | 15 | a0001c0001t0002a0001c0001t0006a0001c0001t0007others(12): Show | 126 | HG00099.hp2 HG00140.hp2 HG00544.hp1 others(123): Show |
3_prime_UTR_variant | MODIFIER | c.*1758G>A | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 14/14 | 1758 | chr14 | 51729787 | |||||
chr14:51729963
|
A | G | 2 | a0001c0001t0006a0001c0001t0023 | 4 | HG01261.hp1 HG02965.hp2 HG03471.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*1934A>G | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 14/14 | 1934 | chr14 | 51729963 | |||||
chr14:51730095
|
T | C | 1 | a0001c0001t0019 | 1 | NA18906.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2066T>C | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 14/14 | 2066 | chr14 | 51730095 | |||||
chr14:51730123
|
A | C | 1 | a0001c0001t0024 | 1 | HG03486.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2094A>C | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 14/14 | 2094 | chr14 | 51730123 | |||||
chr14:51730224
|
T | A | 1 | a0001c0001t0010 | 2 | NA18962.hp2 NA19009.hp1 |
3_prime_UTR_variant | MODIFIER | c.*2195T>A | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 14/14 | 2195 | chr14 | 51730224 | |||||
chr14:51730237
|
G | A | 1 | a0001c0002t0013 | 1 | HG02922.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2208G>A | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 14/14 | 2208 | chr14 | 51730237 | |||||
chr14:51730365
|
A | T | 1 | a0001c0002t0015 | 1 | HG01496.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2336A>T | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 14/14 | 2336 | chr14 | 51730365 | |||||
chr14:51730396
|
G | T | 1 | a0001c0001t0020 | 1 | HG02165.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2367G>T | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 14/14 | 2367 | chr14 | 51730396 | |||||
chr14:51730492
|
A | G | 1 | a0001c0002t0014 | 1 | HG03491.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2463A>G | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 14/14 | 2463 | chr14 | 51730492 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr14:51652017
|
T | C | 1 | a0001c0004t0001g0046 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.-147+21T>C | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 1/13 | chr14 | 51652017 | ||||||
chr14:51652036
|
C | T | 1 | a0001c0001t0002g0315 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.-147+40C>T | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 1/13 | chr14 | 51652036 | ||||||
chr14:51652073
|
T | C | 1 | a0001c0001t0002g0047 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.-147+77T>C | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 1/13 | chr14 | 51652073 | ||||||
chr14:51652082
|
C | T | 4 | a0001c0001t0002g0311a0001c0001t0002g0312a0001c0003t0001g0313others(1): Show | 4 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(1): Show |
intron_variant | MODIFIER | c.-147+86C>T | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 1/13 | chr14 | 51652082 | ||||||
chr14:51652129
|
C | G | 75 | a0001c0001t0002g0253a0001c0001t0002g0285a0001c0001t0002g0294others(72): Show | 94 | HG00438.hp1 HG00544.hp2 HG00735.hp2 others(91): Show |
intron_variant | MODIFIER | c.-147+133C>G | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 1/13 | chr14 | 51652129 | ||||||
chr14:51652250
|
T | C | 29 | a0001c0001t0002g0020a0001c0001t0002g0048a0001c0001t0002g0049others(26): Show | 31 | HG00099.hp2 HG00280.hp1 HG00639.hp1 others(28): Show |
intron_variant | MODIFIER | c.-147+254T>C | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 1/13 | chr14 | 51652250 | ||||||
chr14:51652262
|
G | T | 1 | a0001c0002t0004g0247 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.-147+266G>T | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 1/13 | chr14 | 51652262 | ||||||
chr14:51652278
|
A | G | 1 | a0001c0002t0001g0246 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.-147+282A>G | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 1/13 | chr14 | 51652278 | ||||||
chr14:51652317
|
G | C | 1 | a0001c0002t0001g0074 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.-147+321G>C | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 1/13 | chr14 | 51652317 | ||||||
chr14:51652318
|
G | T | 33 | a0001c0001t0002g0036a0001c0001t0002g0037a0001c0001t0002g0230others(30): Show | 43 | HG00280.hp2 HG00323.hp2 HG00438.hp2 others(40): Show |
intron_variant | MODIFIER | c.-147+322G>T | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 1/13 | chr14 | 51652318 | ||||||
chr14:51652389
|
C | G | 196 | a0001c0001t0001g0202a0001c0001t0001g0209a0001c0001t0002g0012others(193): Show | 237 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(234): Show |
intron_variant | MODIFIER | c.-147+393C>G | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 1/13 | chr14 | 51652389 | ||||||
chr14:51652449
|
C | T | 1 | a0001c0001t0002g0169 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.-147+453C>T | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 1/13 | chr14 | 51652449 | ||||||
chr14:51652507
|
G | A | 19 | a0001c0001t0002g0170a0001c0001t0002g0171a0001c0001t0002g0172others(16): Show | 23 | HG00099.hp1 HG00741.hp2 HG01070.hp1 others(20): Show |
intron_variant | MODIFIER | c.-147+511G>A | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 1/13 | chr14 | 51652507 | ||||||
chr14:51652516
|
G | T | 1 | a0001c0004t0001g0035 | 2 | HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.-147+520G>T | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 1/13 | chr14 | 51652516 | ||||||
chr14:51652518
|
C | G | 19 | a0001c0001t0002g0170a0001c0001t0002g0171a0001c0001t0002g0172others(16): Show | 23 | HG00099.hp1 HG00741.hp2 HG01070.hp1 others(20): Show |
intron_variant | MODIFIER | c.-147+522C>G | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 1/13 | chr14 | 51652518 | ||||||
chr14:51652547
|
C | G | 54 | a0001c0001t0001g0202a0001c0001t0001g0209a0001c0001t0002g0012others(51): Show | 69 | HG00280.hp2 HG00323.hp2 HG00438.hp2 others(66): Show |
intron_variant | MODIFIER | c.-147+551C>G | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 1/13 | chr14 | 51652547 | ||||||
chr14:51652602
|
A | G | 1 | a0001c0013t0001g0201 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.-147+606A>G | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 1/13 | chr14 | 51652602 | ||||||
chr14:51652698
|
A | G | 4 | a0001c0002t0001g0197a0001c0002t0001g0198a0001c0002t0001g0199others(1): Show | 4 | HG02615.hp1 HG02809.hp2 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.-147+702A>G | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 1/13 | chr14 | 51652698 | ||||||
chr14:51652821
|
T | C | 4 | a0001c0001t0002g0048a0001c0001t0002g0049a0001c0001t0002g0050others(1): Show | 4 | HG00738.hp1 HG01256.hp1 HG01515.hp2 others(1): Show |
intron_variant | MODIFIER | c.-147+825T>C | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 1/13 | chr14 | 51652821 | ||||||
chr14:51653065
|
A | G | 1 | a0001c0003t0001g0310 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.-147+1069A>G | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 1/13 | chr14 | 51653065 | ||||||
chr14:51653069
|
C | T | 1 | a0001c0001t0001g0168 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.-147+1073C>T | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 1/13 | chr14 | 51653069 | ||||||
chr14:51653190
|
T | G | 1 | a0001c0002t0001g0075 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.-147+1194T>G | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 1/13 | chr14 | 51653190 | ||||||
chr14:51653205
|
G | GT | 60 | a0001c0001t0001g0202a0001c0001t0001g0209a0001c0001t0002g0012others(57): Show | 75 | HG00280.hp2 HG00323.hp2 HG00438.hp2 others(72): Show |
intron_variant | MODIFIER | c.-147+1210dupT | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr14 | 51653205 | |||||
chr14:51653238
|
G | A | 10 | a0001c0001t0002g0048a0001c0001t0002g0049a0001c0001t0002g0050others(7): Show | 10 | HG00738.hp1 HG01256.hp1 HG01515.hp2 others(7): Show |
intron_variant | MODIFIER | c.-147+1242G>A | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 1/13 | chr14 | 51653238 | ||||||
chr14:51653253
|
G | T | 12 | a0001c0001t0002g0048a0001c0001t0002g0049a0001c0001t0002g0050others(9): Show | 12 | HG00738.hp1 HG01256.hp1 HG01515.hp2 others(9): Show |
intron_variant | MODIFIER | c.-147+1257G>T | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 1/13 | chr14 | 51653253 | ||||||
chr14:51653356
|
A | G | 2 | a0001c0003t0001g0308a0001c0003t0001g0309 | 2 | NA18981.hp1 NA19077.hp2 |
intron_variant | MODIFIER | c.-147+1360A>G | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 1/13 | chr14 | 51653356 | ||||||
chr14:51653437
|
TG | T | 4 | a0001c0002t0001g0197a0001c0002t0001g0198a0001c0002t0001g0199others(1): Show | 4 | HG02615.hp1 HG02809.hp2 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.-147+1445delG | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr14 | 51653437 | |||||
chr14:51653527
|
C | T | 1 | a0001c0006t0003g0167 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.-147+1531C>T | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 1/13 | chr14 | 51653527 | ||||||
chr14:51653546
|
A | G | 196 | a0001c0001t0001g0202a0001c0001t0001g0209a0001c0001t0002g0012others(193): Show | 238 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(235): Show |
intron_variant | MODIFIER | c.-147+1550A>G | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 1/13 | chr14 | 51653546 | ||||||
chr14:51653546
|
A | T | 1 | a0001c0006t0003g0183 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.-147+1550A>T | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 1/13 | chr14 | 51653546 | ||||||
chr14:51653547
|
T | G | 1 | a0001c0003t0001g0248 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.-147+1551T>G | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 1/13 | chr14 | 51653547 | ||||||
chr14:51653596
|
T | A | 27 | a0001c0001t0002g0020a0001c0001t0002g0048a0001c0001t0002g0049others(24): Show | 29 | HG00099.hp2 HG00280.hp1 HG00639.hp1 others(26): Show |
intron_variant | MODIFIER | c.-147+1600T>A | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 1/13 | chr14 | 51653596 | ||||||
chr14:51653607
|
A | T | 1 | a0001c0003t0001g0165 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.-147+1611A>T | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 1/13 | chr14 | 51653607 | ||||||
chr14:51653748
|
G | T | 12 | a0001c0001t0002g0020a0001c0001t0002g0060a0001c0001t0002g0061others(9): Show | 13 | HG00099.hp2 HG00280.hp1 HG00639.hp1 others(10): Show |
intron_variant | MODIFIER | c.-147+1752G>T | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 1/13 | chr14 | 51653748 | ||||||
chr14:51653770
|
A | G | 1 | a0001c0003t0001g0165 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.-147+1774A>G | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 1/13 | chr14 | 51653770 | ||||||
chr14:51653778
|
A | G | 1 | a0001c0003t0001g0165 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.-147+1782A>G | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 1/13 | chr14 | 51653778 | ||||||
chr14:51653786
|
C | T | 2 | a0001c0006t0003g0073a0002c0008t0009g0072 | 2 | HG02572.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.-147+1790C>T | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 1/13 | chr14 | 51653786 | ||||||
chr14:51653844
|
A | G | 3 | a0001c0001t0006g0019a0001c0001t0006g0059a0001c0001t0023g0058 | 4 | HG01261.hp1 HG02965.hp2 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.-147+1848A>G | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 1/13 | chr14 | 51653844 | ||||||
chr14:51653854
|
G | T | 3 | a0001c0002t0001g0193a0001c0003t0001g0194a0001c0013t0001g0201 | 3 | HG02723.hp1 HG06807.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.-147+1858G>T | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 1/13 | chr14 | 51653854 | ||||||
chr14:51654027
|
C | T | 1 | a0001c0001t0001g0164 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.-147+2031C>T | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 1/13 | chr14 | 51654027 | ||||||
chr14:51654102
|
G | A | 1 | a0001c0004t0016g0070 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.-147+2106G>A | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 1/13 | chr14 | 51654102 | ||||||
chr14:51654104
|
A | C | 1 | a0001c0002t0001g0245 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.-147+2108A>C | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 1/13 | chr14 | 51654104 | ||||||
chr14:51654303
|
AT | A | 6 | a0001c0001t0002g0048a0001c0001t0002g0049a0001c0001t0002g0050others(3): Show | 6 | HG00738.hp1 HG01256.hp1 HG01515.hp2 others(3): Show |
intron_variant | MODIFIER | c.-147+2309delT | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr14 | 51654303 | |||||
chr14:51654305
|
T | G | 6 | a0001c0001t0002g0054a0001c0002t0001g0057a0001c0002t0013g0052others(3): Show | 6 | HG02630.hp1 HG02895.hp1 HG02922.hp2 others(3): Show |
intron_variant | MODIFIER | c.-147+2309T>G | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 1/13 | chr14 | 51654305 | ||||||
chr14:51654305
|
T | TG | 110 | a0001c0001t0002g0080a0001c0001t0002g0081a0001c0001t0002g0082others(107): Show | 138 | HG00280.hp1 HG00438.hp1 HG00544.hp1 others(135): Show |
intron_variant | MODIFIER | c.-147+2319dupG | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr14 | 51654305 | |||||
chr14:51654305
|
T | TGG | 58 | a0001c0001t0001g0209a0001c0001t0002g0012a0001c0001t0002g0020others(55): Show | 73 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(70): Show |
intron_variant | MODIFIER | c.-147+2318_-147+231 others(6): Show |
FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr14 | 51654305 | |||||
chr14:51654305
|
T | TGGG | 19 | a0001c0001t0001g0202a0001c0001t0002g0060a0001c0001t0002g0203others(16): Show | 19 | HG00639.hp2 HG01099.hp2 HG01192.hp1 others(16): Show |
intron_variant | MODIFIER | c.-147+2317_-147+231 others(7): Show |
FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr14 | 51654305 | |||||
chr14:51654389
|
A | G | 4 | a0001c0002t0001g0075a0001c0002t0001g0092a0001c0002t0001g0093others(1): Show | 5 | NA18946.hp2 NA18972.hp1 NA18995.hp2 others(2): Show |
intron_variant | MODIFIER | c.-147+2393A>G | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 1/13 | chr14 | 51654389 | ||||||
chr14:51654505
|
A | C | 2 | a0001c0001t0006g0019a0001c0001t0006g0059 | 3 | HG01261.hp1 HG02965.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.-147+2509A>C | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 1/13 | chr14 | 51654505 | ||||||
chr14:51654510
|
C | G | 1 | a0001c0001t0023g0058 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.-147+2514C>G | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 1/13 | chr14 | 51654510 | ||||||
chr14:51654580
|
G | GT | 6 | a0001c0001t0002g0054a0001c0002t0001g0013a0001c0002t0001g0057others(3): Show | 8 | HG01361.hp1 HG01433.hp2 HG02895.hp1 others(5): Show |
intron_variant | MODIFIER | c.-147+2597dupT | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr14 | 51654580 | |||||
chr14:51654580
|
GT | G | 10 | a0001c0001t0006g0019a0001c0001t0006g0059a0001c0001t0023g0058others(7): Show | 11 | HG01167.hp2 HG01257.hp2 HG01261.hp1 others(8): Show |
intron_variant | MODIFIER | c.-147+2597delT | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr14 | 51654580 | |||||
chr14:51654682
|
G | T | 1 | a0001c0001t0002g0253 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.-147+2686G>T | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 1/13 | chr14 | 51654682 | ||||||
chr14:51654766
|
T | C | 1 | a0001c0003t0001g0094 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.-147+2770T>C | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 1/13 | chr14 | 51654766 | ||||||
chr14:51655046
|
TA | T | 42 | a0001c0001t0002g0048a0001c0001t0002g0049a0001c0001t0002g0050others(39): Show | 47 | HG00099.hp1 HG00323.hp2 HG00738.hp1 others(44): Show |
intron_variant | MODIFIER | c.-147+3066delA | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr14 | 51655046 | |||||
chr14:51655086
|
C | T | 1 | a0001c0001t0002g0047 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.-147+3090C>T | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 1/13 | chr14 | 51655086 | ||||||
chr14:51655370
|
A | C | 1 | a0001c0004t0012g0182 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.-147+3374A>C | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 1/13 | chr14 | 51655370 | ||||||
chr14:51655719
|
G | A | 1 | a0001c0003t0001g0258 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.-147+3723G>A | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 1/13 | chr14 | 51655719 | ||||||
chr14:51655759
|
C | T | 71 | a0001c0001t0001g0202a0001c0001t0001g0209a0001c0001t0002g0012others(68): Show | 86 | HG00280.hp2 HG00323.hp2 HG00438.hp2 others(83): Show |
intron_variant | MODIFIER | c.-147+3763C>T | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 1/13 | chr14 | 51655759 | ||||||
chr14:51655861
|
G | A | 2 | a0001c0006t0003g0073a0002c0008t0009g0072 | 2 | HG02572.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.-147+3865G>A | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 1/13 | chr14 | 51655861 | ||||||
chr14:51655901
|
C | T | 59 | a0001c0001t0001g0202a0001c0001t0001g0209a0001c0001t0002g0012others(56): Show | 74 | HG00280.hp2 HG00323.hp2 HG00438.hp2 others(71): Show |
intron_variant | MODIFIER | c.-147+3905C>T | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 1/13 | chr14 | 51655901 | ||||||
chr14:51655914
|
A | G | 1 | a0001c0002t0001g0191 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.-147+3918A>G | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 1/13 | chr14 | 51655914 | ||||||
chr14:51656096
|
A | G | 1 | a0001c0001t0002g0158 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.-147+4100A>G | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 1/13 | chr14 | 51656096 | ||||||
chr14:51656182
|
A | G | 1 | a0001c0002t0001g0166 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.-147+4186A>G | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 1/13 | chr14 | 51656182 | ||||||
chr14:51656221
|
A | G | 1 | a0001c0004t0016g0070 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.-147+4225A>G | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 1/13 | chr14 | 51656221 | ||||||
chr14:51656319
|
T | A | 1 | a0001c0004t0016g0070 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.-147+4323T>A | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 1/13 | chr14 | 51656319 | ||||||
chr14:51656352
|
G | C | 196 | a0001c0001t0001g0202a0001c0001t0001g0209a0001c0001t0002g0012others(193): Show | 237 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(234): Show |
intron_variant | MODIFIER | c.-147+4356G>C | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 1/13 | chr14 | 51656352 | ||||||
chr14:51656355
|
A | T | 71 | a0001c0001t0001g0202a0001c0001t0001g0209a0001c0001t0002g0012others(68): Show | 86 | HG00280.hp2 HG00323.hp2 HG00438.hp2 others(83): Show |
intron_variant | MODIFIER | c.-147+4359A>T | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 1/13 | chr14 | 51656355 | ||||||
chr14:51656369
|
T | G | 2 | a0001c0006t0003g0073a0002c0008t0009g0072 | 2 | HG02572.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.-147+4373T>G | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 1/13 | chr14 | 51656369 | ||||||
chr14:51656430
|
C | T | 313 | a0001c0001t0001g0113a0001c0001t0001g0164a0001c0001t0001g0168others(310): Show | 386 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(383): Show |
intron_variant | MODIFIER | c.-147+4434C>T | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 1/13 | chr14 | 51656430 | ||||||
chr14:51656436
|
C | T | 71 | a0001c0001t0001g0202a0001c0001t0001g0209a0001c0001t0002g0012others(68): Show | 87 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(84): Show |
intron_variant | MODIFIER | c.-147+4440C>T | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 1/13 | chr14 | 51656436 | ||||||
chr14:51656444
|
C | T | 19 | a0001c0001t0002g0170a0001c0001t0002g0171a0001c0001t0002g0172others(16): Show | 23 | HG00099.hp1 HG00741.hp2 HG01070.hp1 others(20): Show |
intron_variant | MODIFIER | c.-147+4448C>T | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 1/13 | chr14 | 51656444 | ||||||
chr14:51656570
|
C | T | 1 | a0001c0002t0001g0241 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.-147+4574C>T | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 1/13 | chr14 | 51656570 | ||||||
chr14:51656664
|
G | A | 1 | a0001c0001t0002g0054 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.-147+4668G>A | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 1/13 | chr14 | 51656664 | ||||||
chr14:51656696
|
G | A | 2 | a0001c0006t0003g0073a0002c0008t0009g0072 | 2 | HG02572.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.-147+4700G>A | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 1/13 | chr14 | 51656696 | ||||||
chr14:51656702
|
G | A | 2 | a0001c0004t0001g0207a0001c0004t0001g0208 | 2 | HG03195.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.-147+4706G>A | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 1/13 | chr14 | 51656702 | ||||||
chr14:51656746
|
G | A | 2 | a0001c0001t0006g0019a0001c0001t0006g0059 | 3 | HG01261.hp1 HG02965.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.-147+4750G>A | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 1/13 | chr14 | 51656746 | ||||||
chr14:51656753
|
C | T | 1 | a0001c0003t0001g0249 | 1 | NA18993.hp2 | intron_variant | MODIFIER | c.-147+4757C>T | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 1/13 | chr14 | 51656753 | ||||||
chr14:51656928
|
A | G | 1 | a0001c0002t0001g0227 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.-147+4932A>G | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 1/13 | chr14 | 51656928 | ||||||
chr14:51656964
|
A | G | 5 | a0001c0001t0002g0010a0001c0001t0002g0155a0001c0001t0002g0156others(2): Show | 8 | HG00673.hp1 HG00738.hp2 HG00741.hp1 others(5): Show |
intron_variant | MODIFIER | c.-147+4968A>G | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 1/13 | chr14 | 51656964 | ||||||
chr14:51657095
|
TATA | T | 5 | a0001c0001t0002g0054a0001c0002t0001g0057a0001c0002t0013g0052others(2): Show | 5 | HG02630.hp1 HG02895.hp1 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.-147+5102_-147+510 others(7): Show |
FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr14 | 51657095 | |||||
chr14:51657110
|
C | T | 1 | a0001c0003t0001g0305 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.-147+5114C>T | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 1/13 | chr14 | 51657110 | ||||||
chr14:51657297
|
G | A | 1 | a0001c0003t0001g0014 | 3 | HG00735.hp2 HG03490.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.-147+5301G>A | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 1/13 | chr14 | 51657297 | ||||||
chr14:51657299
|
G | A | 4 | a0001c0001t0002g0020a0001c0001t0002g0060a0001c0001t0002g0061others(1): Show | 5 | HG00099.hp2 HG01516.hp1 HG01517.hp2 others(2): Show |
intron_variant | MODIFIER | c.-147+5303G>A | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 1/13 | chr14 | 51657299 | ||||||
chr14:51657349
|
C | T | 1 | a0001c0003t0001g0309 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.-147+5353C>T | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 1/13 | chr14 | 51657349 | ||||||
chr14:51657390
|
C | T | 9 | a0001c0003t0001g0045a0001c0004t0001g0046a0001c0004t0001g0063others(6): Show | 10 | HG00280.hp1 HG00639.hp1 HG01109.hp1 others(7): Show |
intron_variant | MODIFIER | c.-147+5394C>T | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 1/13 | chr14 | 51657390 | ||||||
chr14:51657522
|
A | T | 1 | a0001c0002t0001g0217 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.-147+5526A>T | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 1/13 | chr14 | 51657522 | ||||||
chr14:51657533
|
G | A | 1 | a0001c0013t0001g0201 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.-147+5537G>A | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 1/13 | chr14 | 51657533 | ||||||
chr14:51657554
|
G | C | 122 | a0001c0001t0001g0202a0001c0001t0001g0209a0001c0001t0002g0020others(119): Show | 152 | HG00099.hp1 HG00099.hp2 HG00438.hp1 others(149): Show |
intron_variant | MODIFIER | c.-147+5558G>C | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 1/13 | chr14 | 51657554 | ||||||
chr14:51657653
|
C | A | 1 | a0001c0003t0001g0055 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.-147+5657C>A | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 1/13 | chr14 | 51657653 | ||||||
chr14:51657691
|
G | C | 1 | a0001c0004t0001g0035 | 2 | HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.-147+5695G>C | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 1/13 | chr14 | 51657691 | ||||||
chr14:51657703
|
A | G | 205 | a0001c0001t0001g0202a0001c0001t0001g0209a0001c0001t0002g0012others(202): Show | 248 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(245): Show |
intron_variant | MODIFIER | c.-147+5707A>G | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 1/13 | chr14 | 51657703 | ||||||
chr14:51657704
|
A | G | 1 | a0001c0003t0001g0293 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.-147+5708A>G | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 1/13 | chr14 | 51657704 | ||||||
chr14:51657716
|
A | G | 1 | a0001c0002t0001g0142 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.-147+5720A>G | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 1/13 | chr14 | 51657716 | ||||||
chr14:51657790
|
C | G | 1 | a0001c0006t0022g0163 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.-147+5794C>G | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 1/13 | chr14 | 51657790 | ||||||
chr14:51657827
|
GA | G | 4 | a0001c0004t0001g0140a0001c0004t0001g0141a0001c0004t0001g0207others(1): Show | 4 | HG02723.hp2 HG03098.hp1 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.-147+5832delA | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 1/13 | chr14 | 51657827 | ||||||
chr14:51658134
|
G | A | 1 | a0001c0004t0001g0063 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.-147+6138G>A | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 1/13 | chr14 | 51658134 | ||||||
chr14:51658134
|
G | C | 1 | a0001c0004t0001g0056 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.-147+6138G>C | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 1/13 | chr14 | 51658134 | ||||||
chr14:51658154
|
A | G | 10 | a0001c0003t0001g0055a0001c0006t0003g0027a0001c0006t0003g0073others(7): Show | 11 | HG01358.hp1 HG02145.hp2 HG02280.hp2 others(8): Show |
intron_variant | MODIFIER | c.-147+6158A>G | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 1/13 | chr14 | 51658154 | ||||||
chr14:51658245
|
A | G | 31 | a0001c0001t0002g0178a0001c0003t0001g0055a0001c0003t0001g0194others(28): Show | 33 | HG00280.hp1 HG00639.hp1 HG01109.hp1 others(30): Show |
intron_variant | MODIFIER | c.-147+6249A>G | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 1/13 | chr14 | 51658245 | ||||||
chr14:51658326
|
T | TTC | 52 | a0001c0001t0007g0159a0001c0002t0001g0004a0001c0002t0001g0013others(49): Show | 62 | HG00280.hp2 HG00323.hp2 HG00438.hp2 others(59): Show |
intron_variant | MODIFIER | c.-147+6331_-147+633 others(6): Show |
FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr14 | 51658326 | |||||
chr14:51658328
|
T | C | 312 | a0001c0001t0001g0113a0001c0001t0001g0164a0001c0001t0001g0168others(309): Show | 385 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(382): Show |
intron_variant | MODIFIER | c.-147+6332T>C | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 1/13 | chr14 | 51658328 | ||||||
chr14:51658328
|
T | TTC | 3 | a0001c0002t0001g0206a0001c0002t0001g0216a0001c0002t0001g0217 | 3 | HG01884.hp1 HG03139.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.-147+6345_-147+634 others(6): Show |
FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr14 | 51658328 | |||||
chr14:51658375
|
G | T | 1 | a0001c0001t0002g0139 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.-147+6379G>T | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 1/13 | chr14 | 51658375 | ||||||
chr14:51658406
|
CCTCTTGA others(4): Show |
C | 8 | a0001c0004t0001g0046a0001c0004t0001g0063a0001c0004t0001g0064others(5): Show | 8 | HG00280.hp1 HG00639.hp1 HG01109.hp1 others(5): Show |
intron_variant | MODIFIER | c.-147+6417_-147+642 others(15): Show |
FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr14 | 51658406 | |||||
chr14:51658475
|
C | T | 4 | a0001c0004t0005g0185a0001c0004t0005g0187a0001c0004t0005g0190others(1): Show | 4 | HG02083.hp2 NA18994.hp2 NA19055.hp1 others(1): Show |
intron_variant | MODIFIER | c.-147+6479C>T | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 1/13 | chr14 | 51658475 | ||||||
chr14:51658522
|
A | G | 1 | a0001c0003t0001g0194 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.-147+6526A>G | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 1/13 | chr14 | 51658522 | ||||||
chr14:51658613
|
G | A | 10 | a0001c0003t0001g0055a0001c0006t0003g0027a0001c0006t0003g0073others(7): Show | 11 | HG01358.hp1 HG02145.hp2 HG02280.hp2 others(8): Show |
intron_variant | MODIFIER | c.-147+6617G>A | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 1/13 | chr14 | 51658613 | ||||||
chr14:51658664
|
G | A | 20 | a0001c0001t0002g0178a0001c0003t0001g0194a0001c0004t0001g0046others(17): Show | 20 | HG00280.hp1 HG00639.hp1 HG01109.hp1 others(17): Show |
intron_variant | MODIFIER | c.-147+6668G>A | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 1/13 | chr14 | 51658664 | ||||||
chr14:51658664
|
G | T | 1 | a0001c0001t0002g0149 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.-147+6668G>T | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 1/13 | chr14 | 51658664 | ||||||
chr14:51658789
|
A | C | 228 | a0001c0001t0001g0202a0001c0001t0001g0209a0001c0001t0002g0012others(225): Show | 278 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(275): Show |
intron_variant | MODIFIER | c.-147+6793A>C | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 1/13 | chr14 | 51658789 | ||||||
chr14:51658880
|
A | G | 2 | a0001c0001t0002g0178a0001c0004t0012g0182 | 2 | HG01891.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.-147+6884A>G | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 1/13 | chr14 | 51658880 | ||||||
chr14:51658930
|
G | A | 1 | a0001c0003t0001g0254 | 1 | HG01257.hp2 | intron_variant | MODIFIER | c.-147+6934G>A | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 1/13 | chr14 | 51658930 | ||||||
chr14:51658965
|
A | G | 31 | a0001c0001t0002g0178a0001c0003t0001g0055a0001c0003t0001g0194others(28): Show | 33 | HG00280.hp1 HG00639.hp1 HG01109.hp1 others(30): Show |
intron_variant | MODIFIER | c.-147+6969A>G | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 1/13 | chr14 | 51658965 | ||||||
chr14:51659181
|
C | T | 1 | a0003c0010t0001g0071 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.-147+7185C>T | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 1/13 | chr14 | 51659181 | ||||||
chr14:51659635
|
A | G | 6 | a0001c0002t0001g0030a0001c0002t0001g0179a0001c0002t0001g0180others(3): Show | 7 | HG01516.hp2 HG01884.hp2 HG01981.hp1 others(4): Show |
intron_variant | MODIFIER | c.-147+7639A>G | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 1/13 | chr14 | 51659635 | ||||||
chr14:51659679
|
C | T | 1 | a0001c0003t0001g0288 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.-147+7683C>T | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 1/13 | chr14 | 51659679 | ||||||
chr14:51659802
|
A | T | 54 | a0001c0001t0007g0159a0001c0002t0001g0004a0001c0002t0001g0013others(51): Show | 64 | HG00280.hp2 HG00323.hp2 HG00438.hp2 others(61): Show |
intron_variant | MODIFIER | c.-147+7806A>T | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 1/13 | chr14 | 51659802 | ||||||
chr14:51659819
|
A | G | 1 | a0001c0003t0001g0194 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.-147+7823A>G | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 1/13 | chr14 | 51659819 | ||||||
chr14:51659866
|
T | C | 7 | a0001c0001t0001g0202a0001c0001t0001g0209a0001c0001t0002g0012others(4): Show | 9 | HG01074.hp2 HG01099.hp2 HG02451.hp1 others(6): Show |
intron_variant | MODIFIER | c.-147+7870T>C | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 1/13 | chr14 | 51659866 | ||||||
chr14:51659904
|
A | T | 10 | a0001c0003t0001g0055a0001c0006t0003g0027a0001c0006t0003g0073others(7): Show | 11 | HG01358.hp1 HG02145.hp2 HG02280.hp2 others(8): Show |
intron_variant | MODIFIER | c.-147+7908A>T | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 1/13 | chr14 | 51659904 | ||||||
chr14:51659978
|
C | G | 1 | a0001c0004t0016g0070 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.-147+7982C>G | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 1/13 | chr14 | 51659978 | ||||||
chr14:51659982
|
T | C | 1 | a0001c0001t0006g0059 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.-147+7986T>C | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 1/13 | chr14 | 51659982 | ||||||
chr14:51660133
|
C | T | 8 | a0001c0006t0003g0027a0001c0006t0003g0073a0001c0006t0003g0151others(5): Show | 9 | HG01358.hp1 HG02145.hp2 HG02280.hp2 others(6): Show |
intron_variant | MODIFIER | c.-147+8137C>T | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 1/13 | chr14 | 51660133 | ||||||
chr14:51660329
|
A | G | 10 | a0001c0003t0001g0055a0001c0006t0003g0027a0001c0006t0003g0073others(7): Show | 11 | HG01358.hp1 HG02145.hp2 HG02280.hp2 others(8): Show |
intron_variant | MODIFIER | c.-147+8333A>G | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 1/13 | chr14 | 51660329 | ||||||
chr14:51660341
|
A | G | 228 | a0001c0001t0001g0202a0001c0001t0001g0209a0001c0001t0002g0012others(225): Show | 278 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(275): Show |
intron_variant | MODIFIER | c.-147+8345A>G | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 1/13 | chr14 | 51660341 | ||||||
chr14:51660373
|
C | T | 2 | a0001c0001t0002g0061a0001c0001t0002g0062 | 2 | NA18951.hp2 NA18991.hp2 |
intron_variant | MODIFIER | c.-147+8377C>T | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 1/13 | chr14 | 51660373 | ||||||
chr14:51660419
|
C | A | 30 | a0001c0001t0002g0178a0001c0003t0001g0055a0001c0003t0001g0194others(27): Show | 31 | HG00280.hp1 HG00639.hp1 HG01109.hp1 others(28): Show |
intron_variant | MODIFIER | c.-147+8423C>A | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 1/13 | chr14 | 51660419 | ||||||
chr14:51660488
|
A | G | 1 | a0001c0001t0002g0133 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.-147+8492A>G | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 1/13 | chr14 | 51660488 | ||||||
chr14:51660613
|
G | GA | 130 | a0001c0001t0001g0202a0001c0001t0001g0209a0001c0001t0002g0012others(127): Show | 168 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(165): Show |
intron_variant | MODIFIER | c.-147+8635dupA | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr14 | 51660613 | |||||
chr14:51660613
|
G | GAA | 20 | a0001c0002t0001g0092a0001c0003t0001g0022a0001c0003t0001g0077others(17): Show | 21 | HG00280.hp1 HG00639.hp1 HG01109.hp1 others(18): Show |
intron_variant | MODIFIER | c.-147+8634_-147+863 others(6): Show |
FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr14 | 51660613 | |||||
chr14:51660613
|
G | GAAA | 11 | a0001c0003t0001g0055a0001c0003t0001g0076a0001c0003t0001g0078others(8): Show | 12 | HG01358.hp1 HG02145.hp2 HG02280.hp2 others(9): Show |
intron_variant | MODIFIER | c.-147+8633_-147+863 others(7): Show |
FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr14 | 51660613 | |||||
chr14:51660613
|
GA | G | 14 | a0001c0001t0002g0054a0001c0001t0002g0148a0001c0001t0002g0149others(11): Show | 14 | HG01074.hp2 HG01099.hp2 HG02165.hp1 others(11): Show |
intron_variant | MODIFIER | c.-147+8635delA | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr14 | 51660613 | |||||
chr14:51660613
|
GAAA | G | 53 | a0001c0001t0007g0159a0001c0002t0001g0004a0001c0002t0001g0013others(50): Show | 63 | HG00280.hp2 HG00323.hp2 HG00438.hp2 others(60): Show |
intron_variant | MODIFIER | c.-147+8633_-147+863 others(7): Show |
FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr14 | 51660613 | |||||
chr14:51660632
|
T | C | 31 | a0001c0001t0002g0178a0001c0003t0001g0055a0001c0003t0001g0194others(28): Show | 33 | HG00280.hp1 HG00639.hp1 HG01109.hp1 others(30): Show |
intron_variant | MODIFIER | c.-147+8636T>C | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 1/13 | chr14 | 51660632 | ||||||
chr14:51660746
|
T | A | 2 | a0001c0003t0001g0055a0003c0010t0001g0071 | 2 | HG02970.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.-147+8750T>A | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 1/13 | chr14 | 51660746 | ||||||
chr14:51660786
|
T | C | 4 | a0001c0004t0005g0185a0001c0004t0005g0187a0001c0004t0005g0190others(1): Show | 4 | HG02083.hp2 NA18994.hp2 NA19055.hp1 others(1): Show |
intron_variant | MODIFIER | c.-147+8790T>C | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 1/13 | chr14 | 51660786 | ||||||
chr14:51660903
|
G | T | 3 | a0001c0001t0002g0008a0001c0001t0002g0128a0001c0001t0002g0129 | 5 | NA18950.hp2 NA18966.hp2 NA18988.hp2 others(2): Show |
intron_variant | MODIFIER | c.-147+8907G>T | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 1/13 | chr14 | 51660903 | ||||||
chr14:51661119
|
A | G | 140 | a0001c0001t0001g0202a0001c0001t0001g0209a0001c0001t0002g0012others(137): Show | 178 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(175): Show |
intron_variant | MODIFIER | c.-147+9123A>G | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 1/13 | chr14 | 51661119 | ||||||
chr14:51661147
|
G | A | 1 | a0001c0002t0001g0233 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.-147+9151G>A | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 1/13 | chr14 | 51661147 | ||||||
chr14:51661276
|
G | A | 30 | a0001c0001t0002g0178a0001c0003t0001g0055a0001c0003t0001g0194others(27): Show | 31 | HG00280.hp1 HG00639.hp1 HG01109.hp1 others(28): Show |
intron_variant | MODIFIER | c.-147+9280G>A | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 1/13 | chr14 | 51661276 | ||||||
chr14:51661398
|
G | A | 8 | a0001c0001t0002g0047a0001c0001t0002g0143a0001c0001t0002g0144others(5): Show | 8 | HG02109.hp1 HG02280.hp1 HG02486.hp2 others(5): Show |
intron_variant | MODIFIER | c.-147+9402G>A | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 1/13 | chr14 | 51661398 | ||||||
chr14:51661462
|
A | G | 4 | a0001c0004t0001g0140a0001c0004t0001g0141a0001c0004t0001g0207others(1): Show | 4 | HG02723.hp2 HG03098.hp1 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.-147+9466A>G | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 1/13 | chr14 | 51661462 | ||||||
chr14:51661483
|
G | A | 1 | a0003c0010t0001g0071 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.-147+9487G>A | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 1/13 | chr14 | 51661483 | ||||||
chr14:51661889
|
C | T | 4 | a0001c0004t0001g0140a0001c0004t0001g0141a0001c0004t0001g0207others(1): Show | 4 | HG02723.hp2 HG03098.hp1 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.-147+9893C>T | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 1/13 | chr14 | 51661889 | ||||||
chr14:51662057
|
C | T | 2 | a0001c0002t0001g0205a0001c0002t0001g0219 | 2 | HG01516.hp2 HG01981.hp1 |
intron_variant | MODIFIER | c.-147+10061C>T | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 1/13 | chr14 | 51662057 | ||||||
chr14:51662179
|
T | C | 32 | a0001c0001t0002g0178a0001c0002t0001g0196a0001c0003t0001g0055others(29): Show | 34 | HG00280.hp1 HG00639.hp1 HG01109.hp1 others(31): Show |
intron_variant | MODIFIER | c.-147+10183T>C | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 1/13 | chr14 | 51662179 | ||||||
chr14:51662330
|
G | A | 138 | a0001c0001t0001g0202a0001c0001t0001g0209a0001c0001t0002g0012others(135): Show | 176 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(173): Show |
intron_variant | MODIFIER | c.-147+10334G>A | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 1/13 | chr14 | 51662330 | ||||||
chr14:51662787
|
G | T | 22 | a0001c0001t0002g0178a0001c0003t0001g0055a0001c0003t0001g0194others(19): Show | 22 | HG00280.hp1 HG00639.hp1 HG01109.hp1 others(19): Show |
intron_variant | MODIFIER | c.-147+10791G>T | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 1/13 | chr14 | 51662787 | ||||||
chr14:51662953
|
G | A | 2 | a0001c0003t0001g0313a0001c0003t0001g0314 | 2 | HG00140.hp1 HG00323.hp1 |
intron_variant | MODIFIER | c.-147+10957G>A | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 1/13 | chr14 | 51662953 | ||||||
chr14:51662955
|
G | A | 1 | a0001c0002t0001g0205 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.-147+10959G>A | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 1/13 | chr14 | 51662955 | ||||||
chr14:51663184
|
C | A | 225 | a0001c0001t0001g0202a0001c0001t0001g0209a0001c0001t0002g0012others(222): Show | 275 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(272): Show |
intron_variant | MODIFIER | c.-147+11188C>A | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 1/13 | chr14 | 51663184 | ||||||
chr14:51663410
|
A | G | 23 | a0001c0001t0002g0178a0001c0003t0001g0055a0001c0003t0001g0194others(20): Show | 24 | HG00280.hp1 HG00639.hp1 HG01109.hp1 others(21): Show |
intron_variant | MODIFIER | c.-147+11414A>G | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 1/13 | chr14 | 51663410 | ||||||
chr14:51663412
|
A | T | 1 | a0001c0002t0001g0215 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.-147+11416A>T | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 1/13 | chr14 | 51663412 | ||||||
chr14:51663452
|
T | C | 8 | a0001c0006t0003g0027a0001c0006t0003g0073a0001c0006t0003g0151others(5): Show | 9 | HG01358.hp1 HG02145.hp2 HG02280.hp2 others(6): Show |
intron_variant | MODIFIER | c.-147+11456T>C | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 1/13 | chr14 | 51663452 | ||||||
chr14:51663461
|
A | C | 226 | a0001c0001t0001g0202a0001c0001t0001g0209a0001c0001t0002g0012others(223): Show | 276 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(273): Show |
intron_variant | MODIFIER | c.-147+11465A>C | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 1/13 | chr14 | 51663461 | ||||||
chr14:51663605
|
G | T | 1 | a0001c0003t0001g0302 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.-147+11609G>T | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 1/13 | chr14 | 51663605 | ||||||
chr14:51663663
|
G | C | 1 | a0001c0002t0001g0289 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.-147+11667G>C | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 1/13 | chr14 | 51663663 | ||||||
chr14:51663857
|
G | A | 3 | a0001c0003t0001g0015a0001c0003t0001g0263a0001c0003t0001g0264 | 5 | HG01081.hp2 HG01106.hp2 HG01167.hp1 others(2): Show |
intron_variant | MODIFIER | c.-147+11861G>A | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 1/13 | chr14 | 51663857 | ||||||
chr14:51663886
|
G | A | 14 | a0001c0004t0001g0046a0001c0004t0001g0063a0001c0004t0001g0064others(11): Show | 14 | HG00280.hp1 HG00639.hp1 HG01109.hp1 others(11): Show |
intron_variant | MODIFIER | c.-147+11890G>A | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 1/13 | chr14 | 51663886 | ||||||
chr14:51664252
|
G | A | 4 | a0001c0002t0001g0031a0001c0002t0001g0173a0001c0002t0001g0174others(1): Show | 5 | HG00741.hp2 HG01070.hp1 HG01106.hp1 others(2): Show |
intron_variant | MODIFIER | c.-147+12256G>A | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 1/13 | chr14 | 51664252 | ||||||
chr14:51664310
|
G | A | 1 | a0001c0001t0002g0170 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.-147+12314G>A | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 1/13 | chr14 | 51664310 | ||||||
chr14:51664375
|
A | G | 1 | a0001c0002t0001g0090 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.-147+12379A>G | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 1/13 | chr14 | 51664375 | ||||||
chr14:51664396
|
C | T | 4 | a0001c0004t0005g0185a0001c0004t0005g0187a0001c0004t0005g0190others(1): Show | 4 | HG02083.hp2 NA18994.hp2 NA19055.hp1 others(1): Show |
intron_variant | MODIFIER | c.-147+12400C>T | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 1/13 | chr14 | 51664396 | ||||||
chr14:51664422
|
A | C | 8 | a0001c0006t0003g0027a0001c0006t0003g0073a0001c0006t0003g0151others(5): Show | 9 | HG01358.hp1 HG02145.hp2 HG02280.hp2 others(6): Show |
intron_variant | MODIFIER | c.-147+12426A>C | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 1/13 | chr14 | 51664422 | ||||||
chr14:51664481
|
C | T | 1 | a0001c0004t0001g0035 | 2 | HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.-147+12485C>T | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 1/13 | chr14 | 51664481 | ||||||
chr14:51664854
|
CAGTTAGT others(3): Show |
C | 1 | a0001c0002t0001g0083 | 1 | NA18951.hp1 | intron_variant | MODIFIER | c.-147+12860_-147+12 others(16): Show |
FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr14 | 51664854 | |||||
chr14:51664866
|
A | C | 1 | a0001c0002t0001g0083 | 1 | NA18951.hp1 | intron_variant | MODIFIER | c.-147+12870A>C | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 1/13 | chr14 | 51664866 | ||||||
chr14:51665025
|
G | T | 22 | a0001c0001t0002g0178a0001c0003t0001g0055a0001c0003t0001g0194others(19): Show | 22 | HG00280.hp1 HG00639.hp1 HG01109.hp1 others(19): Show |
intron_variant | MODIFIER | c.-147+13029G>T | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 1/13 | chr14 | 51665025 | ||||||
chr14:51665038
|
G | A | 53 | a0001c0002t0001g0004a0001c0002t0001g0013a0001c0002t0001g0028others(50): Show | 64 | HG00280.hp2 HG00323.hp2 HG00438.hp2 others(61): Show |
intron_variant | MODIFIER | c.-147+13042G>A | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 1/13 | chr14 | 51665038 | ||||||
chr14:51665215
|
G | T | 8 | a0001c0006t0003g0027a0001c0006t0003g0073a0001c0006t0003g0151others(5): Show | 9 | HG01358.hp1 HG02145.hp2 HG02280.hp2 others(6): Show |
intron_variant | MODIFIER | c.-147+13219G>T | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 1/13 | chr14 | 51665215 | ||||||
chr14:51665218
|
G | A | 1 | a0001c0004t0001g0207 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.-147+13222G>A | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 1/13 | chr14 | 51665218 | ||||||
chr14:51665237
|
C | A | 1 | a0003c0010t0001g0071 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.-147+13241C>A | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 1/13 | chr14 | 51665237 | ||||||
chr14:51665238
|
C | T | 4 | a0001c0004t0005g0185a0001c0004t0005g0187a0001c0004t0005g0190others(1): Show | 4 | HG02083.hp2 NA18994.hp2 NA19055.hp1 others(1): Show |
intron_variant | MODIFIER | c.-147+13242C>T | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 1/13 | chr14 | 51665238 | ||||||
chr14:51665279
|
C | A | 2 | a0001c0002t0004g0038a0001c0002t0004g0222 | 3 | HG01069.hp2 HG01071.hp2 HG01192.hp2 |
intron_variant | MODIFIER | c.-147+13283C>A | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 1/13 | chr14 | 51665279 | ||||||
chr14:51665287
|
G | T | 1 | a0001c0013t0001g0201 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.-147+13291G>T | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 1/13 | chr14 | 51665287 | ||||||
chr14:51665483
|
G | A | 22 | a0001c0001t0002g0178a0001c0003t0001g0055a0001c0003t0001g0194others(19): Show | 22 | HG00280.hp1 HG00639.hp1 HG01109.hp1 others(19): Show |
intron_variant | MODIFIER | c.-147+13487G>A | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 1/13 | chr14 | 51665483 | ||||||
chr14:51665501
|
CT | C | 2 | a0001c0003t0001g0040a0001c0003t0001g0041 | 4 | NA18970.hp2 NA19002.hp1 NA19085.hp2 others(1): Show |
intron_variant | MODIFIER | c.-147+13507delT | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr14 | 51665501 | |||||
chr14:51665514
|
C | T | 8 | a0001c0006t0003g0027a0001c0006t0003g0073a0001c0006t0003g0151others(5): Show | 9 | HG01358.hp1 HG02145.hp2 HG02280.hp2 others(6): Show |
intron_variant | MODIFIER | c.-147+13518C>T | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 1/13 | chr14 | 51665514 | ||||||
chr14:51665518
|
C | T | 1 | a0001c0003t0001g0045 | 2 | HG03239.hp2 HG03710.hp1 |
intron_variant | MODIFIER | c.-147+13522C>T | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 1/13 | chr14 | 51665518 | ||||||
chr14:51665613
|
A | G | 104 | a0001c0001t0001g0202a0001c0001t0001g0209a0001c0001t0002g0012others(101): Show | 132 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(129): Show |
intron_variant | MODIFIER | c.-147+13617A>G | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 1/13 | chr14 | 51665613 | ||||||
chr14:51665667
|
T | A | 1 | a0001c0003t0001g0212 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.-147+13671T>A | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 1/13 | chr14 | 51665667 | ||||||
chr14:51665701
|
C | T | 1 | a0001c0002t0002g0226 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.-147+13705C>T | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 1/13 | chr14 | 51665701 | ||||||
chr14:51665769
|
T | C | 9 | a0001c0001t0002g0178a0001c0003t0001g0055a0001c0003t0001g0194others(6): Show | 10 | HG01433.hp1 HG01891.hp2 HG02258.hp2 others(7): Show |
intron_variant | MODIFIER | c.-147+13773T>C | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 1/13 | chr14 | 51665769 | ||||||
chr14:51665787
|
G | A | 1 | a0001c0001t0002g0048 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.-147+13791G>A | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 1/13 | chr14 | 51665787 | ||||||
chr14:51665906
|
C | T | 1 | a0001c0002t0001g0191 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.-147+13910C>T | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 1/13 | chr14 | 51665906 | ||||||
chr14:51665979
|
G | A | 4 | a0001c0004t0001g0140a0001c0004t0001g0141a0001c0004t0001g0207others(1): Show | 4 | HG02723.hp2 HG03098.hp1 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.-147+13983G>A | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 1/13 | chr14 | 51665979 | ||||||
chr14:51666109
|
T | C | 1 | a0002c0008t0009g0072 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.-147+14113T>C | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 1/13 | chr14 | 51666109 | ||||||
chr14:51666332
|
A | G | 4 | a0001c0002t0001g0030a0001c0002t0001g0179a0001c0002t0001g0180others(1): Show | 5 | HG01884.hp2 HG02451.hp2 HG02630.hp2 others(2): Show |
intron_variant | MODIFIER | c.-147+14336A>G | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 1/13 | chr14 | 51666332 | ||||||
chr14:51666410
|
T | A | 1 | a0001c0006t0003g0073 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.-147+14414T>A | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 1/13 | chr14 | 51666410 | ||||||
chr14:51666428
|
A | G | 3 | a0001c0002t0001g0206a0001c0002t0001g0216a0001c0002t0001g0217 | 3 | HG01884.hp1 HG03139.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.-147+14432A>G | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 1/13 | chr14 | 51666428 | ||||||
chr14:51666515
|
G | A | 27 | a0001c0001t0002g0178a0001c0004t0001g0046a0001c0004t0001g0063others(24): Show | 28 | HG00280.hp1 HG00639.hp1 HG01109.hp1 others(25): Show |
intron_variant | MODIFIER | c.-147+14519G>A | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 1/13 | chr14 | 51666515 | ||||||
chr14:51666750
|
T | A | 1 | a0001c0002t0017g0213 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.-147+14754T>A | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 1/13 | chr14 | 51666750 | ||||||
chr14:51666926
|
G | A | 1 | a0001c0002t0001g0223 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.-147+14930G>A | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 1/13 | chr14 | 51666926 | ||||||
chr14:51667006
|
G | A | 6 | a0001c0001t0002g0178a0001c0004t0012g0182a0001c0004t0016g0070others(3): Show | 6 | HG01433.hp1 HG01891.hp2 HG02258.hp2 others(3): Show |
intron_variant | MODIFIER | c.-147+15010G>A | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 1/13 | chr14 | 51667006 | ||||||
chr14:51667039
|
C | T | 1 | a0001c0001t0002g0026 | 2 | NA18984.hp2 NA19090.hp1 |
intron_variant | MODIFIER | c.-147+15043C>T | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 1/13 | chr14 | 51667039 | ||||||
chr14:51667060
|
G | A | 1 | a0001c0003t0001g0055 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.-147+15064G>A | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 1/13 | chr14 | 51667060 | ||||||
chr14:51667080
|
G | C | 79 | a0001c0003t0001g0006a0001c0003t0001g0011a0001c0003t0001g0014others(76): Show | 100 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(97): Show |
intron_variant | MODIFIER | c.-147+15084G>C | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 1/13 | chr14 | 51667080 | ||||||
chr14:51667282
|
C | A | 9 | a0001c0004t0001g0046a0001c0004t0001g0063a0001c0004t0001g0064others(6): Show | 9 | HG00280.hp1 HG00639.hp1 HG01109.hp1 others(6): Show |
intron_variant | MODIFIER | c.-147+15286C>A | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 1/13 | chr14 | 51667282 | ||||||
chr14:51667360
|
C | T | 2 | a0001c0002t0014g0243a0001c0002t0015g0240 | 2 | HG01496.hp1 HG03491.hp1 |
intron_variant | MODIFIER | c.-147+15364C>T | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 1/13 | chr14 | 51667360 | ||||||
chr14:51667378
|
T | C | 1 | a0001c0003t0001g0305 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.-147+15382T>C | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 1/13 | chr14 | 51667378 | ||||||
chr14:51667636
|
C | T | 13 | a0001c0001t0002g0047a0001c0001t0002g0048a0001c0001t0002g0049others(10): Show | 13 | HG00738.hp1 HG01168.hp2 HG01256.hp1 others(10): Show |
intron_variant | MODIFIER | c.-147+15640C>T | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 1/13 | chr14 | 51667636 | ||||||
chr14:51667669
|
C | A | 217 | a0001c0001t0001g0113a0001c0001t0001g0164a0001c0001t0001g0168others(214): Show | 267 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(264): Show |
intron_variant | MODIFIER | c.-147+15673C>A | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 1/13 | chr14 | 51667669 | ||||||
chr14:51668316
|
T | C | 1 | a0001c0002t0001g0074 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.-147+16320T>C | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 1/13 | chr14 | 51668316 | ||||||
chr14:51668405
|
C | G | 1 | a0001c0002t0001g0225 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.-147+16409C>G | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 1/13 | chr14 | 51668405 | ||||||
chr14:51668438
|
T | C | 6 | a0001c0006t0003g0027a0001c0006t0003g0151a0001c0006t0003g0152others(3): Show | 7 | HG01358.hp1 HG02145.hp2 HG02280.hp2 others(4): Show |
intron_variant | MODIFIER | c.-147+16442T>C | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 1/13 | chr14 | 51668438 | ||||||
chr14:51668466
|
C | T | 5 | a0001c0002t0001g0074a0001c0004t0001g0140a0001c0004t0001g0141others(2): Show | 5 | HG02723.hp2 HG03098.hp1 HG03195.hp1 others(2): Show |
intron_variant | MODIFIER | c.-147+16470C>T | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 1/13 | chr14 | 51668466 | ||||||
chr14:51668496
|
G | C | 1 | a0001c0002t0001g0220 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.-147+16500G>C | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 1/13 | chr14 | 51668496 | ||||||
chr14:51668634
|
G | A | 1 | a0001c0002t0001g0084 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.-147+16638G>A | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 1/13 | chr14 | 51668634 | ||||||
chr14:51668638
|
G | A | 141 | a0001c0001t0001g0113a0001c0001t0001g0164a0001c0001t0001g0168others(138): Show | 171 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(168): Show |
intron_variant | MODIFIER | c.-147+16642G>A | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 1/13 | chr14 | 51668638 | ||||||
chr14:51668818
|
C | T | 1 | a0002c0008t0009g0291 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.-147+16822C>T | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 1/13 | chr14 | 51668818 | ||||||
chr14:51668868
|
C | T | 3 | a0001c0001t0011g0131a0001c0001t0011g0132a0001c0001t0024g0124 | 3 | HG02896.hp2 HG02897.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.-147+16872C>T | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 1/13 | chr14 | 51668868 | ||||||
chr14:51669055
|
A | G | 2 | a0001c0002t0001g0205a0001c0002t0001g0219 | 2 | HG01516.hp2 HG01981.hp1 |
intron_variant | MODIFIER | c.-147+17059A>G | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 1/13 | chr14 | 51669055 | ||||||
chr14:51669058
|
T | C | 2 | a0001c0003t0001g0098a0001c0003t0001g0099 | 2 | HG03453.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.-147+17062T>C | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 1/13 | chr14 | 51669058 | ||||||
chr14:51669172
|
T | TATCTGGC others(720): Show |
2 | a0001c0004t0005g0185a0001c0004t0005g0187 | 2 | HG02083.hp2 NA18994.hp2 |
intron_variant | MODIFIER | c.-147+17196_-147+17 others(733): Show |
FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr14 | 51669172 | |||||
chr14:51669172
|
T | TATCTGGC others(721): Show |
2 | a0001c0004t0005g0190a0001c0004t0005g0292 | 2 | NA19055.hp1 NA19082.hp2 |
intron_variant | MODIFIER | c.-147+17196_-147+17 others(734): Show |
FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr14 | 51669172 | |||||
chr14:51669492
|
A | G | 1 | a0001c0003t0001g0310 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.-147+17496A>G | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 1/13 | chr14 | 51669492 | ||||||
chr14:51669514
|
G | T | 1 | a0001c0001t0002g0172 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.-147+17518G>T | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 1/13 | chr14 | 51669514 | ||||||
chr14:51669849
|
G | GCAAAATT others(315): Show |
8 | a0001c0006t0003g0027a0001c0006t0003g0073a0001c0006t0003g0151others(5): Show | 9 | HG01358.hp1 HG02145.hp2 HG02280.hp2 others(6): Show |
intron_variant | MODIFIER | c.-147+17863_-147+17 others(328): Show |
FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr14 | 51669849 | |||||
chr14:51669994
|
C | T | 77 | a0001c0003t0001g0006a0001c0003t0001g0011a0001c0003t0001g0014others(74): Show | 97 | HG00140.hp1 HG00323.hp1 HG00438.hp1 others(94): Show |
intron_variant | MODIFIER | c.-147+17998C>T | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 1/13 | chr14 | 51669994 | ||||||
chr14:51670012
|
C | T | 109 | a0001c0001t0001g0113a0001c0001t0001g0164a0001c0001t0001g0168others(106): Show | 138 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(135): Show |
intron_variant | MODIFIER | c.-147+18016C>T | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 1/13 | chr14 | 51670012 | ||||||
chr14:51670037
|
A | C | 9 | a0001c0004t0001g0046a0001c0004t0001g0063a0001c0004t0001g0064others(6): Show | 9 | HG00280.hp1 HG00639.hp1 HG01109.hp1 others(6): Show |
intron_variant | MODIFIER | c.-147+18041A>C | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 1/13 | chr14 | 51670037 | ||||||
chr14:51670039
|
A | T | 2 | a0001c0001t0002g0037a0001c0001t0002g0312 | 3 | HG01256.hp2 HG01258.hp2 HG02109.hp2 |
intron_variant | MODIFIER | c.-147+18043A>T | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 1/13 | chr14 | 51670039 | ||||||
chr14:51670070
|
G | T | 109 | a0001c0001t0001g0113a0001c0001t0001g0164a0001c0001t0001g0168others(106): Show | 138 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(135): Show |
intron_variant | MODIFIER | c.-147+18074G>T | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 1/13 | chr14 | 51670070 | ||||||
chr14:51670098
|
G | A | 1 | a0001c0003t0001g0299 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.-147+18102G>A | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 1/13 | chr14 | 51670098 | ||||||
chr14:51670124
|
T | G | 4 | a0001c0004t0005g0185a0001c0004t0005g0187a0001c0004t0005g0190others(1): Show | 4 | HG02083.hp2 NA18994.hp2 NA19055.hp1 others(1): Show |
intron_variant | MODIFIER | c.-147+18128T>G | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 1/13 | chr14 | 51670124 | ||||||
chr14:51670255
|
A | T | 2 | a0001c0001t0002g0061a0001c0001t0002g0062 | 2 | NA18951.hp2 NA18991.hp2 |
intron_variant | MODIFIER | c.-147+18259A>T | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 1/13 | chr14 | 51670255 | ||||||
chr14:51670350
|
A | G | 110 | a0001c0001t0001g0113a0001c0001t0001g0164a0001c0001t0001g0168others(107): Show | 139 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(136): Show |
intron_variant | MODIFIER | c.-147+18354A>G | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 1/13 | chr14 | 51670350 | ||||||
chr14:51670398
|
G | T | 1 | a0001c0001t0002g0123 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.-147+18402G>T | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 1/13 | chr14 | 51670398 | ||||||
chr14:51670530
|
A | G | 1 | a0001c0002t0001g0227 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.-147+18534A>G | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 1/13 | chr14 | 51670530 | ||||||
chr14:51670707
|
G | A | 4 | a0001c0004t0005g0185a0001c0004t0005g0187a0001c0004t0005g0190others(1): Show | 4 | HG02083.hp2 NA18994.hp2 NA19055.hp1 others(1): Show |
intron_variant | MODIFIER | c.-147+18711G>A | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 1/13 | chr14 | 51670707 | ||||||
chr14:51670749
|
G | A | 1 | a0001c0001t0002g0230 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.-147+18753G>A | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 1/13 | chr14 | 51670749 | ||||||
chr14:51670809
|
C | T | 1 | a0001c0001t0001g0202 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.-147+18813C>T | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 1/13 | chr14 | 51670809 | ||||||
chr14:51670823
|
T | C | 14 | a0001c0004t0005g0185a0001c0004t0005g0187a0001c0004t0005g0190others(11): Show | 15 | HG01358.hp1 HG02083.hp2 HG02145.hp2 others(12): Show |
intron_variant | MODIFIER | c.-147+18827T>C | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 1/13 | chr14 | 51670823 | ||||||
chr14:51670860
|
T | A | 2 | a0002c0008t0009g0072a0002c0008t0009g0291 | 2 | HG02258.hp2 HG02572.hp2 |
intron_variant | MODIFIER | c.-146-18831T>A | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 1/13 | chr14 | 51670860 | ||||||
chr14:51670926
|
C | T | 5 | a0001c0004t0001g0140a0001c0004t0001g0141a0001c0004t0001g0207others(2): Show | 5 | HG02723.hp2 HG02818.hp2 HG03098.hp1 others(2): Show |
intron_variant | MODIFIER | c.-146-18765C>T | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 1/13 | chr14 | 51670926 | ||||||
chr14:51670936
|
C | T | 1 | a0001c0002t0001g0214 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.-146-18755C>T | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 1/13 | chr14 | 51670936 | ||||||
chr14:51670937
|
G | A | 2 | a0001c0002t0002g0204a0001c0005t0001g0300 | 2 | HG02523.hp2 HG03942.hp2 |
intron_variant | MODIFIER | c.-146-18754G>A | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 1/13 | chr14 | 51670937 | ||||||
chr14:51670943
|
G | A | 5 | a0001c0006t0003g0027a0001c0006t0003g0151a0001c0006t0003g0152others(2): Show | 6 | HG01358.hp1 HG02145.hp2 HG02280.hp2 others(3): Show |
intron_variant | MODIFIER | c.-146-18748G>A | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 1/13 | chr14 | 51670943 | ||||||
chr14:51671038
|
T | G | 222 | a0001c0001t0001g0113a0001c0001t0001g0164a0001c0001t0001g0168others(219): Show | 273 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(270): Show |
intron_variant | MODIFIER | c.-146-18653T>G | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 1/13 | chr14 | 51671038 | ||||||
chr14:51671050
|
A | T | 2 | a0001c0002t0001g0205a0001c0002t0001g0219 | 2 | HG01516.hp2 HG01981.hp1 |
intron_variant | MODIFIER | c.-146-18641A>T | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 1/13 | chr14 | 51671050 | ||||||
chr14:51671069
|
C | G | 3 | a0001c0001t0002g0020a0001c0001t0002g0060a0001c0001t0002g0158 | 4 | HG00099.hp2 HG01516.hp1 HG01517.hp2 others(1): Show |
intron_variant | MODIFIER | c.-146-18622C>G | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 1/13 | chr14 | 51671069 | ||||||
chr14:51671155
|
A | G | 2 | a0001c0001t0002g0026a0001c0002t0001g0217 | 3 | HG03516.hp1 NA18984.hp2 NA19090.hp1 |
intron_variant | MODIFIER | c.-146-18536A>G | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 1/13 | chr14 | 51671155 | ||||||
chr14:51671177
|
C | T | 3 | a0001c0003t0001g0015a0001c0003t0001g0263a0001c0003t0001g0264 | 5 | HG01081.hp2 HG01106.hp2 HG01167.hp1 others(2): Show |
intron_variant | MODIFIER | c.-146-18514C>T | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 1/13 | chr14 | 51671177 | ||||||
chr14:51671279
|
T | TC | 29 | a0001c0001t0002g0178a0001c0003t0001g0055a0001c0004t0001g0035others(26): Show | 31 | HG00280.hp1 HG00639.hp1 HG01109.hp1 others(28): Show |
intron_variant | MODIFIER | c.-146-18412_-146-18 others(7): Show |
FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 1/13 | chr14 | 51671279 | ||||||
chr14:51671342
|
G | C | 9 | a0001c0002t0001g0296a0001c0005t0001g0005a0001c0005t0001g0009others(6): Show | 14 | HG02074.hp1 HG02523.hp2 NA18944.hp1 others(11): Show |
intron_variant | MODIFIER | c.-146-18349G>C | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 1/13 | chr14 | 51671342 | ||||||
chr14:51671376
|
C | T | 1 | a0001c0001t0002g0147 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.-146-18315C>T | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 1/13 | chr14 | 51671376 | ||||||
chr14:51671459
|
T | C | 4 | a0001c0004t0001g0140a0001c0004t0001g0141a0001c0004t0001g0207others(1): Show | 4 | HG02723.hp2 HG03098.hp1 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.-146-18232T>C | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 1/13 | chr14 | 51671459 | ||||||
chr14:51671524
|
A | G | 4 | a0001c0001t0001g0168a0001c0001t0002g0082a0001c0001t0002g0121others(1): Show | 4 | HG00544.hp1 HG02135.hp1 HG02523.hp1 others(1): Show |
intron_variant | MODIFIER | c.-146-18167A>G | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 1/13 | chr14 | 51671524 | ||||||
chr14:51671527
|
G | T | 1 | a0001c0002t0001g0189 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.-146-18164G>T | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 1/13 | chr14 | 51671527 | ||||||
chr14:51671569
|
G | A | 1 | a0001c0003t0001g0266 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.-146-18122G>A | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 1/13 | chr14 | 51671569 | ||||||
chr14:51671676
|
C | T | 220 | a0001c0001t0001g0113a0001c0001t0001g0164a0001c0001t0001g0168others(217): Show | 271 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(268): Show |
intron_variant | MODIFIER | c.-146-18015C>T | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 1/13 | chr14 | 51671676 | ||||||
chr14:51671901
|
T | G | 1 | a0001c0003t0001g0100 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.-146-17790T>G | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 1/13 | chr14 | 51671901 | ||||||
chr14:51671930
|
A | G | 111 | a0001c0001t0001g0113a0001c0001t0001g0164a0001c0001t0001g0168others(108): Show | 140 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(137): Show |
intron_variant | MODIFIER | c.-146-17761A>G | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 1/13 | chr14 | 51671930 | ||||||
chr14:51672079
|
T | C | 1 | a0001c0003t0001g0055 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.-146-17612T>C | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 1/13 | chr14 | 51672079 | ||||||
chr14:51672136
|
A | G | 2 | a0001c0004t0016g0070a0001c0006t0022g0163 | 2 | HG01433.hp1 HG02818.hp2 |
intron_variant | MODIFIER | c.-146-17555A>G | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 1/13 | chr14 | 51672136 | ||||||
chr14:51672417
|
C | T | 1 | a0001c0005t0001g0307 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.-146-17274C>T | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 1/13 | chr14 | 51672417 | ||||||
chr14:51672488
|
C | A | 1 | a0001c0002t0001g0091 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.-146-17203C>A | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 1/13 | chr14 | 51672488 | ||||||
chr14:51672607
|
G | T | 1 | a0001c0003t0001g0175 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.-146-17084G>T | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 1/13 | chr14 | 51672607 | ||||||
chr14:51672886
|
C | T | 3 | a0001c0001t0006g0019a0001c0001t0006g0059a0001c0001t0023g0058 | 4 | HG01261.hp1 HG02965.hp2 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.-146-16805C>T | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 1/13 | chr14 | 51672886 | ||||||
chr14:51673067
|
G | A | 8 | a0001c0004t0001g0046a0001c0004t0001g0063a0001c0004t0001g0064others(5): Show | 8 | HG00280.hp1 HG00639.hp1 HG01109.hp1 others(5): Show |
intron_variant | MODIFIER | c.-146-16624G>A | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 1/13 | chr14 | 51673067 | ||||||
chr14:51673237
|
C | G | 2 | a0001c0002t0001g0214a0001c0003t0001g0212 | 2 | HG02615.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.-146-16454C>G | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 1/13 | chr14 | 51673237 | ||||||
chr14:51673323
|
T | A | 1 | a0001c0003t0001g0267 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.-146-16368T>A | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 1/13 | chr14 | 51673323 | ||||||
chr14:51673337
|
T | G | 224 | a0001c0001t0001g0113a0001c0001t0001g0164a0001c0001t0001g0168others(221): Show | 276 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(273): Show |
intron_variant | MODIFIER | c.-146-16354T>G | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 1/13 | chr14 | 51673337 | ||||||
chr14:51673546
|
T | G | 6 | a0001c0003t0001g0257a0001c0003t0001g0259a0001c0003t0001g0260others(3): Show | 6 | HG02015.hp1 NA18953.hp1 NA18962.hp1 others(3): Show |
intron_variant | MODIFIER | c.-146-16145T>G | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 1/13 | chr14 | 51673546 | ||||||
chr14:51673704
|
T | C | 8 | a0001c0006t0003g0027a0001c0006t0003g0073a0001c0006t0003g0151others(5): Show | 9 | HG01358.hp1 HG02145.hp2 HG02280.hp2 others(6): Show |
intron_variant | MODIFIER | c.-146-15987T>C | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 1/13 | chr14 | 51673704 | ||||||
chr14:51673978
|
A | T | 1 | a0001c0003t0001g0255 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.-146-15713A>T | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 1/13 | chr14 | 51673978 | ||||||
chr14:51673979
|
T | C | 1 | a0001c0002t0001g0134 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.-146-15712T>C | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 1/13 | chr14 | 51673979 | ||||||
chr14:51674253
|
C | T | 1 | a0001c0004t0001g0208 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.-146-15438C>T | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 1/13 | chr14 | 51674253 | ||||||
chr14:51674420
|
T | C | 1 | a0001c0002t0008g0016 | 3 | NA18957.hp2 NA18961.hp2 NA19063.hp2 |
intron_variant | MODIFIER | c.-146-15271T>C | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 1/13 | chr14 | 51674420 | ||||||
chr14:51674460
|
C | T | 1 | a0004c0012t0002g0210 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.-146-15231C>T | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 1/13 | chr14 | 51674460 | ||||||
chr14:51674626
|
T | C | 1 | a0001c0004t0001g0035 | 2 | HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.-146-15065T>C | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 1/13 | chr14 | 51674626 | ||||||
chr14:51674748
|
G | A | 1 | a0001c0013t0001g0201 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.-146-14943G>A | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 1/13 | chr14 | 51674748 | ||||||
chr14:51674927
|
A | G | 13 | a0001c0001t0002g0047a0001c0001t0002g0048a0001c0001t0002g0049others(10): Show | 13 | HG00738.hp1 HG01168.hp2 HG01256.hp1 others(10): Show |
intron_variant | MODIFIER | c.-146-14764A>G | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 1/13 | chr14 | 51674927 | ||||||
chr14:51674929
|
G | T | 27 | a0001c0001t0002g0178a0001c0004t0001g0046a0001c0004t0001g0063others(24): Show | 28 | HG00280.hp1 HG00639.hp1 HG01109.hp1 others(25): Show |
intron_variant | MODIFIER | c.-146-14762G>T | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 1/13 | chr14 | 51674929 | ||||||
chr14:51674955
|
G | A | 140 | a0001c0001t0001g0113a0001c0001t0001g0164a0001c0001t0001g0168others(137): Show | 170 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(167): Show |
intron_variant | MODIFIER | c.-146-14736G>A | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 1/13 | chr14 | 51674955 | ||||||
chr14:51674984
|
G | T | 3 | a0001c0001t0007g0095a0001c0001t0007g0096a0001c0001t0007g0159 | 3 | HG00733.hp2 HG01109.hp2 HG01261.hp2 |
intron_variant | MODIFIER | c.-146-14707G>T | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 1/13 | chr14 | 51674984 | ||||||
chr14:51675132
|
G | A | 1 | a0001c0001t0002g0294 | 1 | NA18947.hp1 | intron_variant | MODIFIER | c.-146-14559G>A | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 1/13 | chr14 | 51675132 | ||||||
chr14:51675221
|
C | T | 1 | a0001c0002t0001g0166 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.-146-14470C>T | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 1/13 | chr14 | 51675221 | ||||||
chr14:51675564
|
T | C | 1 | a0001c0013t0001g0201 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.-146-14127T>C | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 1/13 | chr14 | 51675564 | ||||||
chr14:51676001
|
A | T | 1 | a0001c0003t0001g0041 | 2 | NA18970.hp2 NA19090.hp2 |
intron_variant | MODIFIER | c.-146-13690A>T | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 1/13 | chr14 | 51676001 | ||||||
chr14:51676013
|
C | T | 1 | a0001c0002t0001g0245 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.-146-13678C>T | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 1/13 | chr14 | 51676013 | ||||||
chr14:51676029
|
G | A | 4 | a0001c0002t0001g0092a0001c0004t0001g0046a0001c0004t0001g0064others(1): Show | 4 | HG00639.hp1 HG01109.hp1 HG02723.hp1 others(1): Show |
intron_variant | MODIFIER | c.-146-13662G>A | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 1/13 | chr14 | 51676029 | ||||||
chr14:51676088
|
T | G | 1 | a0001c0002t0001g0227 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.-146-13603T>G | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 1/13 | chr14 | 51676088 | ||||||
chr14:51676120
|
A | T | 1 | a0001c0001t0002g0120 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.-146-13571A>T | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 1/13 | chr14 | 51676120 | ||||||
chr14:51676168
|
G | C | 133 | a0001c0001t0001g0113a0001c0001t0001g0164a0001c0001t0001g0168others(130): Show | 161 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(158): Show |
intron_variant | MODIFIER | c.-146-13523G>C | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 1/13 | chr14 | 51676168 | ||||||
chr14:51676514
|
G | T | 1 | a0001c0004t0012g0182 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.-146-13177G>T | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 1/13 | chr14 | 51676514 | ||||||
chr14:51676805
|
T | G | 1 | a0001c0004t0012g0182 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.-146-12886T>G | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 1/13 | chr14 | 51676805 | ||||||
chr14:51676881
|
C | T | 1 | a0001c0002t0001g0137 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.-146-12810C>T | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 1/13 | chr14 | 51676881 | ||||||
chr14:51676960
|
A | G | 1 | a0001c0004t0001g0035 | 2 | HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.-146-12731A>G | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 1/13 | chr14 | 51676960 | ||||||
chr14:51676976
|
C | T | 130 | a0001c0001t0001g0113a0001c0001t0001g0164a0001c0001t0001g0168others(127): Show | 158 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(155): Show |
intron_variant | MODIFIER | c.-146-12715C>T | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 1/13 | chr14 | 51676976 | ||||||
chr14:51677121
|
G | T | 1 | a0001c0002t0001g0239 | 1 | NA19054.hp2 | intron_variant | MODIFIER | c.-146-12570G>T | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 1/13 | chr14 | 51677121 | ||||||
chr14:51677424
|
G | A | 2 | a0001c0003t0001g0194a0003c0010t0001g0071 | 2 | HG03139.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.-146-12267G>A | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 1/13 | chr14 | 51677424 | ||||||
chr14:51677697
|
T | C | 1 | a0001c0002t0001g0090 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.-146-11994T>C | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 1/13 | chr14 | 51677697 | ||||||
chr14:51677719
|
A | G | 215 | a0001c0001t0001g0113a0001c0001t0001g0164a0001c0001t0001g0168others(212): Show | 264 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(261): Show |
intron_variant | MODIFIER | c.-146-11972A>G | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 1/13 | chr14 | 51677719 | ||||||
chr14:51677726
|
G | A | 1 | a0001c0004t0012g0182 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.-146-11965G>A | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 1/13 | chr14 | 51677726 | ||||||
chr14:51677875
|
T | C | 279 | a0001c0001t0001g0113a0001c0001t0001g0164a0001c0001t0001g0168others(276): Show | 342 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(339): Show |
intron_variant | MODIFIER | c.-146-11816T>C | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 1/13 | chr14 | 51677875 | ||||||
chr14:51678154
|
T | C | 119 | a0001c0001t0001g0113a0001c0001t0001g0164a0001c0001t0001g0168others(116): Show | 146 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(143): Show |
intron_variant | MODIFIER | c.-146-11537T>C | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 1/13 | chr14 | 51678154 | ||||||
chr14:51678287
|
G | C | 4 | a0001c0004t0001g0140a0001c0004t0001g0141a0001c0004t0001g0207others(1): Show | 4 | HG02723.hp2 HG03098.hp1 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.-146-11404G>C | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 1/13 | chr14 | 51678287 | ||||||
chr14:51678387
|
T | C | 283 | a0001c0001t0001g0113a0001c0001t0001g0164a0001c0001t0001g0168others(280): Show | 346 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(343): Show |
intron_variant | MODIFIER | c.-146-11304T>C | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 1/13 | chr14 | 51678387 | ||||||
chr14:51678427
|
A | G | 1 | a0001c0003t0001g0045 | 2 | HG03239.hp2 HG03710.hp1 |
intron_variant | MODIFIER | c.-146-11264A>G | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 1/13 | chr14 | 51678427 | ||||||
chr14:51678526
|
T | C | 120 | a0001c0001t0001g0113a0001c0001t0001g0164a0001c0001t0001g0168others(117): Show | 147 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(144): Show |
intron_variant | MODIFIER | c.-146-11165T>C | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 1/13 | chr14 | 51678526 | ||||||
chr14:51678597
|
G | A | 1 | a0001c0001t0002g0102 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.-146-11094G>A | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 1/13 | chr14 | 51678597 | ||||||
chr14:51678941
|
C | T | 101 | a0001c0001t0001g0113a0001c0001t0001g0164a0001c0001t0001g0168others(98): Show | 127 | HG00099.hp2 HG00140.hp2 HG00544.hp1 others(124): Show |
intron_variant | MODIFIER | c.-146-10750C>T | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 1/13 | chr14 | 51678941 | ||||||
chr14:51678978
|
T | G | 1 | a0001c0003t0001g0041 | 2 | NA18970.hp2 NA19090.hp2 |
intron_variant | MODIFIER | c.-146-10713T>G | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 1/13 | chr14 | 51678978 | ||||||
chr14:51679044
|
G | A | 1 | a0001c0013t0001g0201 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.-146-10647G>A | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 1/13 | chr14 | 51679044 | ||||||
chr14:51679131
|
C | G | 1 | a0001c0004t0016g0070 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.-146-10560C>G | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 1/13 | chr14 | 51679131 | ||||||
chr14:51679271
|
T | G | 1 | a0001c0003t0001g0212 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.-146-10420T>G | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 1/13 | chr14 | 51679271 | ||||||
chr14:51679299
|
C | CAT | 314 | a0001c0001t0001g0113a0001c0001t0001g0164a0001c0001t0001g0168others(311): Show | 386 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(383): Show |
intron_variant | MODIFIER | c.-146-10392_-146-10 others(8): Show |
FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 1/13 | chr14 | 51679299 | ||||||
chr14:51679406
|
G | T | 50 | a0001c0002t0001g0004a0001c0002t0001g0013a0001c0002t0001g0025others(47): Show | 60 | HG00280.hp2 HG00438.hp2 HG00639.hp2 others(57): Show |
intron_variant | MODIFIER | c.-146-10285G>T | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 1/13 | chr14 | 51679406 | ||||||
chr14:51679555
|
C | CT | 8 | a0001c0002t0001g0142a0001c0003t0001g0078a0001c0003t0001g0250others(5): Show | 8 | HG01175.hp1 HG02027.hp2 HG02723.hp2 others(5): Show |
intron_variant | MODIFIER | c.-146-10118dupT | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr14 | 51679555 | |||||
chr14:51679555
|
CT | C | 17 | a0001c0001t0002g0003a0001c0001t0002g0117a0001c0001t0002g0118others(14): Show | 22 | HG01515.hp1 HG02083.hp2 HG02258.hp2 others(19): Show |
intron_variant | MODIFIER | c.-146-10118delT | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr14 | 51679555 | |||||
chr14:51679555
|
CTT | C | 103 | a0001c0001t0001g0113a0001c0001t0001g0164a0001c0001t0001g0168others(100): Show | 125 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(122): Show |
intron_variant | MODIFIER | c.-146-10119_-146-10 others(8): Show |
FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr14 | 51679555 | |||||
chr14:51679735
|
C | G | 4 | a0001c0002t0004g0038a0001c0002t0004g0222a0001c0002t0004g0238others(1): Show | 5 | HG00280.hp2 HG01069.hp2 HG01071.hp2 others(2): Show |
intron_variant | MODIFIER | c.-146-9956C>G | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 1/13 | chr14 | 51679735 | ||||||
chr14:51679737
|
T | G | 5 | a0001c0003t0001g0017a0001c0003t0001g0228a0001c0003t0001g0271others(2): Show | 7 | HG01070.hp2 HG01071.hp1 HG01123.hp1 others(4): Show |
intron_variant | MODIFIER | c.-146-9954T>G | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 1/13 | chr14 | 51679737 | ||||||
chr14:51679881
|
C | T | 1 | a0001c0003t0001g0194 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.-146-9810C>T | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 1/13 | chr14 | 51679881 | ||||||
chr14:51680104
|
T | C | 316 | a0001c0001t0001g0113a0001c0001t0001g0164a0001c0001t0001g0168others(313): Show | 389 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(386): Show |
intron_variant | MODIFIER | c.-146-9587T>C | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 1/13 | chr14 | 51680104 | ||||||
chr14:51680119
|
G | A | 3 | a0001c0001t0002g0020a0001c0001t0002g0060a0001c0001t0002g0158 | 4 | HG00099.hp2 HG01516.hp1 HG01517.hp2 others(1): Show |
intron_variant | MODIFIER | c.-146-9572G>A | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 1/13 | chr14 | 51680119 | ||||||
chr14:51680764
|
AT | A | 127 | a0001c0001t0001g0113a0001c0001t0001g0164a0001c0001t0001g0168others(124): Show | 154 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(151): Show |
intron_variant | MODIFIER | c.-146-8920delT | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr14 | 51680764 | |||||
chr14:51680813
|
T | G | 1 | a0001c0001t0019g0103 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.-146-8878T>G | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 1/13 | chr14 | 51680813 | ||||||
chr14:51681123
|
C | T | 4 | a0001c0004t0001g0140a0001c0004t0001g0141a0001c0004t0001g0207others(1): Show | 4 | HG02723.hp2 HG03098.hp1 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.-146-8568C>T | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 1/13 | chr14 | 51681123 | ||||||
chr14:51681300
|
A | G | 2 | a0002c0008t0009g0072a0002c0008t0009g0291 | 2 | HG02258.hp2 HG02572.hp2 |
intron_variant | MODIFIER | c.-146-8391A>G | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 1/13 | chr14 | 51681300 | ||||||
chr14:51681362
|
TG | T | 4 | a0001c0004t0001g0140a0001c0004t0001g0141a0001c0004t0001g0207others(1): Show | 4 | HG02723.hp2 HG03098.hp1 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.-146-8328delG | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 1/13 | chr14 | 51681362 | ||||||
chr14:51681366
|
G | C | 1 | a0001c0003t0001g0259 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.-146-8325G>C | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 1/13 | chr14 | 51681366 | ||||||
chr14:51681598
|
A | G | 2 | a0002c0008t0009g0072a0002c0008t0009g0291 | 2 | HG02258.hp2 HG02572.hp2 |
intron_variant | MODIFIER | c.-146-8093A>G | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 1/13 | chr14 | 51681598 | ||||||
chr14:51681898
|
T | C | 1 | a0001c0001t0019g0103 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.-146-7793T>C | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 1/13 | chr14 | 51681898 | ||||||
chr14:51681938
|
T | G | 1 | a0001c0003t0001g0077 | 1 | NA18972.hp2 | intron_variant | MODIFIER | c.-146-7753T>G | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 1/13 | chr14 | 51681938 | ||||||
chr14:51681976
|
C | T | 1 | a0001c0001t0002g0230 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.-146-7715C>T | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 1/13 | chr14 | 51681976 | ||||||
chr14:51682032
|
T | C | 1 | a0001c0007t0001g0053 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.-146-7659T>C | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 1/13 | chr14 | 51682032 | ||||||
chr14:51682040
|
A | G | 3 | a0001c0004t0016g0070a0002c0008t0009g0072a0002c0008t0009g0291 | 3 | HG02258.hp2 HG02572.hp2 HG02818.hp2 |
intron_variant | MODIFIER | c.-146-7651A>G | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 1/13 | chr14 | 51682040 | ||||||
chr14:51682091
|
A | G | 1 | a0001c0001t0002g0156 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.-146-7600A>G | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 1/13 | chr14 | 51682091 | ||||||
chr14:51682234
|
C | A | 1 | a0001c0002t0001g0166 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.-146-7457C>A | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 1/13 | chr14 | 51682234 | ||||||
chr14:51682499
|
G | C | 4 | a0001c0004t0012g0182a0001c0004t0016g0070a0002c0008t0009g0072others(1): Show | 4 | HG02258.hp2 HG02572.hp2 HG02818.hp2 others(1): Show |
intron_variant | MODIFIER | c.-146-7192G>C | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 1/13 | chr14 | 51682499 | ||||||
chr14:51682576
|
T | G | 4 | a0001c0004t0005g0185a0001c0004t0005g0187a0001c0004t0005g0190others(1): Show | 4 | HG02083.hp2 NA18994.hp2 NA19055.hp1 others(1): Show |
intron_variant | MODIFIER | c.-146-7115T>G | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 1/13 | chr14 | 51682576 | ||||||
chr14:51682773
|
C | T | 1 | a0001c0013t0001g0201 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.-146-6918C>T | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 1/13 | chr14 | 51682773 | ||||||
chr14:51682822
|
A | G | 1 | a0001c0002t0001g0150 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.-146-6869A>G | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 1/13 | chr14 | 51682822 | ||||||
chr14:51682925
|
G | A | 1 | a0001c0002t0001g0176 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.-146-6766G>A | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 1/13 | chr14 | 51682925 | ||||||
chr14:51682930
|
C | T | 118 | a0001c0001t0001g0113a0001c0001t0001g0164a0001c0001t0001g0168others(115): Show | 145 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(142): Show |
intron_variant | MODIFIER | c.-146-6761C>T | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 1/13 | chr14 | 51682930 | ||||||
chr14:51682960
|
A | G | 1 | a0001c0003t0001g0287 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.-146-6731A>G | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 1/13 | chr14 | 51682960 | ||||||
chr14:51683037
|
C | A | 2 | a0001c0003t0001g0194a0003c0010t0001g0071 | 2 | HG03139.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.-146-6654C>A | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 1/13 | chr14 | 51683037 | ||||||
chr14:51683045
|
C | G | 1 | a0001c0002t0001g0244 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.-146-6646C>G | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 1/13 | chr14 | 51683045 | ||||||
chr14:51683050
|
T | C | 121 | a0001c0001t0001g0113a0001c0001t0001g0164a0001c0001t0001g0168others(118): Show | 148 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(145): Show |
intron_variant | MODIFIER | c.-146-6641T>C | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 1/13 | chr14 | 51683050 | ||||||
chr14:51683079
|
A | G | 1 | a0001c0004t0001g0056 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.-146-6612A>G | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 1/13 | chr14 | 51683079 | ||||||
chr14:51683116
|
A | G | 81 | a0001c0002t0001g0166a0001c0003t0001g0006a0001c0003t0001g0011others(78): Show | 102 | HG00140.hp1 HG00323.hp1 HG00438.hp1 others(99): Show |
intron_variant | MODIFIER | c.-146-6575A>G | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 1/13 | chr14 | 51683116 | ||||||
chr14:51683161
|
T | C | 1 | a0001c0004t0012g0182 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.-146-6530T>C | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 1/13 | chr14 | 51683161 | ||||||
chr14:51683348
|
CAGCAATG others(5): Show |
C | 1 | a0001c0003t0001g0305 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.-146-6339_-146-632 others(16): Show |
FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr14 | 51683348 | |||||
chr14:51683367
|
T | G | 1 | a0001c0003t0001g0305 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.-146-6324T>G | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 1/13 | chr14 | 51683367 | ||||||
chr14:51683368
|
C | G | 1 | a0001c0003t0001g0305 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.-146-6323C>G | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 1/13 | chr14 | 51683368 | ||||||
chr14:51683369
|
T | A | 1 | a0001c0003t0001g0305 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.-146-6322T>A | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 1/13 | chr14 | 51683369 | ||||||
chr14:51683370
|
C | G | 1 | a0001c0003t0001g0305 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.-146-6321C>G | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 1/13 | chr14 | 51683370 | ||||||
chr14:51683371
|
C | A | 1 | a0001c0003t0001g0305 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.-146-6320C>A | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 1/13 | chr14 | 51683371 | ||||||
chr14:51683445
|
AT | A | 119 | a0001c0001t0001g0113a0001c0001t0001g0164a0001c0001t0001g0168others(116): Show | 145 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(142): Show |
intron_variant | MODIFIER | c.-146-6233delT | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr14 | 51683445 | |||||
chr14:51683479
|
G | A | 1 | a0004c0012t0002g0210 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.-146-6212G>A | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 1/13 | chr14 | 51683479 | ||||||
chr14:51683489
|
G | C | 82 | a0001c0002t0001g0166a0001c0003t0001g0006a0001c0003t0001g0011others(79): Show | 103 | HG00140.hp1 HG00323.hp1 HG00438.hp1 others(100): Show |
intron_variant | MODIFIER | c.-146-6202G>C | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 1/13 | chr14 | 51683489 | ||||||
chr14:51683572
|
C | T | 1 | a0001c0004t0001g0035 | 2 | HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.-146-6119C>T | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 1/13 | chr14 | 51683572 | ||||||
chr14:51683687
|
G | A | 118 | a0001c0001t0001g0113a0001c0001t0001g0164a0001c0001t0001g0168others(115): Show | 144 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(141): Show |
intron_variant | MODIFIER | c.-146-6004G>A | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 1/13 | chr14 | 51683687 | ||||||
chr14:51683692
|
A | G | 1 | a0001c0002t0001g0177 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.-146-5999A>G | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 1/13 | chr14 | 51683692 | ||||||
chr14:51683895
|
T | C | 1 | a0001c0004t0012g0182 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.-146-5796T>C | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 1/13 | chr14 | 51683895 | ||||||
chr14:51684117
|
G | A | 3 | a0001c0003t0001g0259a0001c0003t0001g0260a0001c0003t0001g0261 | 3 | NA18953.hp1 NA18990.hp2 NA19081.hp1 |
intron_variant | MODIFIER | c.-146-5574G>A | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 1/13 | chr14 | 51684117 | ||||||
chr14:51684146
|
T | C | 2 | a0002c0008t0009g0072a0002c0008t0009g0291 | 2 | HG02258.hp2 HG02572.hp2 |
intron_variant | MODIFIER | c.-146-5545T>C | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 1/13 | chr14 | 51684146 | ||||||
chr14:51684158
|
C | T | 1 | a0001c0004t0005g0185 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.-146-5533C>T | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 1/13 | chr14 | 51684158 | ||||||
chr14:51684161
|
T | TA | 6 | a0001c0002t0001g0091a0001c0002t0001g0127a0001c0002t0014g0243others(3): Show | 6 | HG01496.hp1 HG02040.hp1 HG03098.hp2 others(3): Show |
intron_variant | MODIFIER | c.-146-5517dupA | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr14 | 51684161 | |||||
chr14:51684161
|
TA | T | 118 | a0001c0001t0001g0113a0001c0001t0001g0164a0001c0001t0001g0168others(115): Show | 144 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(141): Show |
intron_variant | MODIFIER | c.-146-5517delA | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr14 | 51684161 | |||||
chr14:51684180
|
A | G | 2 | a0001c0003t0001g0194a0003c0010t0001g0071 | 2 | HG03139.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.-146-5511A>G | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 1/13 | chr14 | 51684180 | ||||||
chr14:51684222
|
G | A | 1 | a0002c0008t0009g0291 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.-146-5469G>A | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 1/13 | chr14 | 51684222 | ||||||
chr14:51684486
|
G | A | 100 | a0001c0001t0001g0113a0001c0001t0001g0164a0001c0001t0001g0168others(97): Show | 126 | HG00099.hp2 HG00140.hp2 HG00544.hp1 others(123): Show |
intron_variant | MODIFIER | c.-146-5205G>A | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 1/13 | chr14 | 51684486 | ||||||
chr14:51684557
|
C | T | 4 | a0001c0004t0005g0185a0001c0004t0005g0187a0001c0004t0005g0190others(1): Show | 4 | HG02083.hp2 NA18994.hp2 NA19055.hp1 others(1): Show |
intron_variant | MODIFIER | c.-146-5134C>T | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 1/13 | chr14 | 51684557 | ||||||
chr14:51684621
|
A | G | 118 | a0001c0001t0001g0113a0001c0001t0001g0164a0001c0001t0001g0168others(115): Show | 144 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(141): Show |
intron_variant | MODIFIER | c.-146-5070A>G | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 1/13 | chr14 | 51684621 | ||||||
chr14:51684728
|
C | T | 1 | a0001c0003t0001g0212 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.-146-4963C>T | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 1/13 | chr14 | 51684728 | ||||||
chr14:51684752
|
T | C | 4 | a0001c0004t0001g0140a0001c0004t0001g0141a0001c0004t0001g0207others(1): Show | 4 | HG02723.hp2 HG03098.hp1 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.-146-4939T>C | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 1/13 | chr14 | 51684752 | ||||||
chr14:51684756
|
A | T | 80 | a0001c0003t0001g0006a0001c0003t0001g0011a0001c0003t0001g0014others(77): Show | 100 | HG00140.hp1 HG00323.hp1 HG00438.hp1 others(97): Show |
intron_variant | MODIFIER | c.-146-4935A>T | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 1/13 | chr14 | 51684756 | ||||||
chr14:51684821
|
T | G | 1 | a0001c0006t0003g0151 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.-146-4870T>G | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 1/13 | chr14 | 51684821 | ||||||
chr14:51684907
|
G | A | 2 | a0001c0002t0014g0243a0001c0002t0015g0240 | 2 | HG01496.hp1 HG03491.hp1 |
intron_variant | MODIFIER | c.-146-4784G>A | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 1/13 | chr14 | 51684907 | ||||||
chr14:51685159
|
A | G | 1 | a0001c0001t0002g0116 | 1 | NA18993.hp1 | intron_variant | MODIFIER | c.-146-4532A>G | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 1/13 | chr14 | 51685159 | ||||||
chr14:51685186
|
T | C | 1 | a0001c0004t0012g0182 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.-146-4505T>C | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 1/13 | chr14 | 51685186 | ||||||
chr14:51685464
|
G | A | 1 | a0001c0004t0016g0070 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.-146-4227G>A | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 1/13 | chr14 | 51685464 | ||||||
chr14:51685582
|
A | G | 4 | a0001c0001t0002g0012a0001c0001t0002g0203a0001c0001t0002g0211others(1): Show | 6 | HG01074.hp2 HG01099.hp2 HG02809.hp1 others(3): Show |
intron_variant | MODIFIER | c.-146-4109A>G | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 1/13 | chr14 | 51685582 | ||||||
chr14:51685803
|
G | A | 4 | a0001c0004t0001g0140a0001c0004t0001g0141a0001c0004t0001g0207others(1): Show | 4 | HG02723.hp2 HG03098.hp1 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.-146-3888G>A | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 1/13 | chr14 | 51685803 | ||||||
chr14:51685819
|
TA | T | 118 | a0001c0001t0001g0113a0001c0001t0001g0164a0001c0001t0001g0168others(115): Show | 144 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(141): Show |
intron_variant | MODIFIER | c.-146-3870delA | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr14 | 51685819 | |||||
chr14:51685883
|
G | A | 118 | a0001c0001t0001g0113a0001c0001t0001g0164a0001c0001t0001g0168others(115): Show | 144 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(141): Show |
intron_variant | MODIFIER | c.-146-3808G>A | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 1/13 | chr14 | 51685883 | ||||||
chr14:51686019
|
C | T | 1 | a0001c0002t0001g0166 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.-146-3672C>T | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 1/13 | chr14 | 51686019 | ||||||
chr14:51686106
|
T | A | 118 | a0001c0001t0001g0113a0001c0001t0001g0164a0001c0001t0001g0168others(115): Show | 144 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(141): Show |
intron_variant | MODIFIER | c.-146-3585T>A | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 1/13 | chr14 | 51686106 | ||||||
chr14:51686152
|
T | TA | 82 | a0001c0002t0001g0166a0001c0003t0001g0006a0001c0003t0001g0011others(79): Show | 103 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(100): Show |
intron_variant | MODIFIER | c.-146-3537dupA | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr14 | 51686152 | |||||
chr14:51686779
|
T | A | 1 | a0001c0004t0016g0070 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.-146-2912T>A | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 1/13 | chr14 | 51686779 | ||||||
chr14:51686806
|
A | G | 1 | a0001c0001t0002g0122 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.-146-2885A>G | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 1/13 | chr14 | 51686806 | ||||||
chr14:51686858
|
TTAAG | T | 4 | a0001c0003t0001g0098a0001c0003t0001g0099a0001c0007t0001g0053others(1): Show | 4 | HG02630.hp1 HG03453.hp1 HG03540.hp2 others(1): Show |
intron_variant | MODIFIER | c.-146-2831_-146-282 others(8): Show |
FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr14 | 51686858 | |||||
chr14:51686894
|
A | G | 2 | a0002c0008t0009g0072a0002c0008t0009g0291 | 2 | HG02258.hp2 HG02572.hp2 |
intron_variant | MODIFIER | c.-146-2797A>G | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 1/13 | chr14 | 51686894 | ||||||
chr14:51687054
|
C | A | 118 | a0001c0001t0001g0113a0001c0001t0001g0164a0001c0001t0001g0168others(115): Show | 144 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(141): Show |
intron_variant | MODIFIER | c.-146-2637C>A | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 1/13 | chr14 | 51687054 | ||||||
chr14:51687087
|
C | T | 118 | a0001c0001t0001g0113a0001c0001t0001g0164a0001c0001t0001g0168others(115): Show | 144 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(141): Show |
intron_variant | MODIFIER | c.-146-2604C>T | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 1/13 | chr14 | 51687087 | ||||||
chr14:51687238
|
A | T | 81 | a0001c0002t0001g0166a0001c0003t0001g0006a0001c0003t0001g0011others(78): Show | 102 | HG00140.hp1 HG00323.hp1 HG00438.hp1 others(99): Show |
intron_variant | MODIFIER | c.-146-2453A>T | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 1/13 | chr14 | 51687238 | ||||||
chr14:51687336
|
A | G | 1 | a0003c0010t0001g0071 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.-146-2355A>G | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 1/13 | chr14 | 51687336 | ||||||
chr14:51687359
|
G | A | 1 | a0003c0010t0001g0071 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.-146-2332G>A | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 1/13 | chr14 | 51687359 | ||||||
chr14:51687539
|
T | G | 9 | a0001c0006t0003g0027a0001c0006t0003g0073a0001c0006t0003g0151others(6): Show | 10 | HG01358.hp1 HG01433.hp1 HG02145.hp2 others(7): Show |
intron_variant | MODIFIER | c.-146-2152T>G | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 1/13 | chr14 | 51687539 | ||||||
chr14:51687542
|
T | TA | 4 | a0001c0004t0001g0140a0001c0004t0001g0141a0001c0004t0001g0207others(1): Show | 4 | HG02723.hp2 HG03098.hp1 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.-146-2148dupA | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr14 | 51687542 | |||||
chr14:51687632
|
C | G | 4 | a0001c0003t0001g0098a0001c0003t0001g0099a0001c0007t0001g0053others(1): Show | 4 | HG02630.hp1 HG03453.hp1 HG03540.hp2 others(1): Show |
intron_variant | MODIFIER | c.-146-2059C>G | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 1/13 | chr14 | 51687632 | ||||||
chr14:51687644
|
C | T | 1 | a0001c0003t0001g0266 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.-146-2047C>T | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 1/13 | chr14 | 51687644 | ||||||
chr14:51687654
|
T | C | 1 | a0001c0002t0001g0246 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.-146-2037T>C | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 1/13 | chr14 | 51687654 | ||||||
chr14:51687779
|
C | T | 2 | a0001c0003t0001g0194a0003c0010t0001g0071 | 2 | HG03139.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.-146-1912C>T | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 1/13 | chr14 | 51687779 | ||||||
chr14:51687809
|
A | T | 1 | a0001c0001t0002g0315 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.-146-1882A>T | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 1/13 | chr14 | 51687809 | ||||||
chr14:51687859
|
A | C | 13 | a0001c0001t0001g0202a0001c0001t0001g0209a0001c0001t0002g0012others(10): Show | 16 | HG00099.hp2 HG01074.hp2 HG01099.hp2 others(13): Show |
intron_variant | MODIFIER | c.-146-1832A>C | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 1/13 | chr14 | 51687859 | ||||||
chr14:51687894
|
C | G | 1 | a0001c0002t0001g0186 | 1 | NA19055.hp2 | intron_variant | MODIFIER | c.-146-1797C>G | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 1/13 | chr14 | 51687894 | ||||||
chr14:51687914
|
T | G | 1 | a0001c0003t0001g0269 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.-146-1777T>G | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 1/13 | chr14 | 51687914 | ||||||
chr14:51688114
|
G | A | 2 | a0002c0008t0009g0072a0002c0008t0009g0291 | 2 | HG02258.hp2 HG02572.hp2 |
intron_variant | MODIFIER | c.-146-1577G>A | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 1/13 | chr14 | 51688114 | ||||||
chr14:51688128
|
T | G | 102 | a0001c0001t0001g0113a0001c0001t0001g0164a0001c0001t0001g0168others(99): Show | 128 | HG00099.hp2 HG00140.hp2 HG00544.hp1 others(125): Show |
intron_variant | MODIFIER | c.-146-1563T>G | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 1/13 | chr14 | 51688128 | ||||||
chr14:51688159
|
T | C | 3 | a0001c0001t0006g0019a0001c0001t0006g0059a0001c0001t0023g0058 | 4 | HG01261.hp1 HG02965.hp2 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.-146-1532T>C | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 1/13 | chr14 | 51688159 | ||||||
chr14:51688327
|
A | C | 2 | a0001c0003t0001g0194a0003c0010t0001g0071 | 2 | HG03139.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.-146-1364A>C | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 1/13 | chr14 | 51688327 | ||||||
chr14:51688361
|
TCGAGTAA others(4): Show |
T | 1 | a0001c0004t0005g0292 | 1 | NA19055.hp1 | intron_variant | MODIFIER | c.-146-1328_-146-131 others(15): Show |
FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr14 | 51688361 | |||||
chr14:51688362
|
C | T | 1 | a0001c0003t0001g0302 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.-146-1329C>T | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 1/13 | chr14 | 51688362 | ||||||
chr14:51688363
|
G | A | 1 | a0001c0001t0002g0315 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.-146-1328G>A | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 1/13 | chr14 | 51688363 | ||||||
chr14:51688444
|
A | G | 2 | a0002c0008t0009g0072a0002c0008t0009g0291 | 2 | HG02258.hp2 HG02572.hp2 |
intron_variant | MODIFIER | c.-146-1247A>G | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 1/13 | chr14 | 51688444 | ||||||
chr14:51688459
|
C | G | 2 | a0002c0008t0009g0072a0002c0008t0009g0291 | 2 | HG02258.hp2 HG02572.hp2 |
intron_variant | MODIFIER | c.-146-1232C>G | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 1/13 | chr14 | 51688459 | ||||||
chr14:51688527
|
C | T | 1 | a0001c0006t0003g0153 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.-146-1164C>T | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 1/13 | chr14 | 51688527 | ||||||
chr14:51688630
|
C | T | 1 | a0001c0004t0016g0070 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.-146-1061C>T | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 1/13 | chr14 | 51688630 | ||||||
chr14:51688763
|
T | C | 1 | a0001c0002t0001g0179 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.-146-928T>C | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 1/13 | chr14 | 51688763 | ||||||
chr14:51688874
|
A | G | 1 | a0001c0003t0001g0138 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.-146-817A>G | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 1/13 | chr14 | 51688874 | ||||||
chr14:51688977
|
AT | A | 3 | a0001c0002t0001g0025a0001c0002t0001g0125a0001c0002t0001g0142 | 4 | HG02027.hp2 NA18945.hp1 NA18953.hp2 others(1): Show |
intron_variant | MODIFIER | c.-146-708delT | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr14 | 51688977 | |||||
chr14:51689123
|
G | A | 1 | a0001c0005t0001g0300 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.-146-568G>A | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 1/13 | chr14 | 51689123 | ||||||
chr14:51689128
|
G | T | 1 | a0001c0002t0001g0214 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.-146-563G>T | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 1/13 | chr14 | 51689128 | ||||||
chr14:51689267
|
T | C | 9 | a0001c0004t0001g0046a0001c0004t0001g0063a0001c0004t0001g0064others(6): Show | 9 | HG00280.hp1 HG00639.hp1 HG01109.hp1 others(6): Show |
intron_variant | MODIFIER | c.-146-424T>C | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 1/13 | chr14 | 51689267 | ||||||
chr14:51689279
|
C | G | 17 | a0001c0004t0001g0046a0001c0004t0001g0063a0001c0004t0001g0064others(14): Show | 17 | HG00280.hp1 HG00639.hp1 HG01109.hp1 others(14): Show |
intron_variant | MODIFIER | c.-146-412C>G | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 1/13 | chr14 | 51689279 | ||||||
chr14:51689423
|
G | T | 117 | a0001c0001t0001g0113a0001c0001t0001g0164a0001c0001t0001g0168others(114): Show | 143 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(140): Show |
intron_variant | MODIFIER | c.-146-268G>T | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 1/13 | chr14 | 51689423 | ||||||
chr14:51689652
|
C | T | 4 | a0001c0004t0001g0140a0001c0004t0001g0141a0001c0004t0001g0207others(1): Show | 4 | HG02723.hp2 HG03098.hp1 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.-146-39C>T | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 1/13 | chr14 | 51689652 | ||||||
chr14:51690144
|
A | G | 1 | a0001c0001t0019g0103 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.99+209A>G | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 2/13 | chr14 | 51690144 | ||||||
chr14:51690334
|
T | C | 4 | a0001c0004t0001g0140a0001c0004t0001g0141a0001c0004t0001g0207others(1): Show | 4 | HG02723.hp2 HG03098.hp1 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.99+399T>C | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 2/13 | chr14 | 51690334 | ||||||
chr14:51690417
|
A | G | 1 | a0001c0001t0002g0195 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.99+482A>G | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 2/13 | chr14 | 51690417 | ||||||
chr14:51690662
|
G | A | 1 | a0001c0002t0001g0075 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.99+727G>A | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 2/13 | chr14 | 51690662 | ||||||
chr14:51690747
|
A | G | 1 | a0001c0003t0001g0262 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.99+812A>G | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 2/13 | chr14 | 51690747 | ||||||
chr14:51690850
|
A | AT | 19 | a0001c0002t0001g0196a0001c0004t0001g0035a0001c0004t0001g0046others(16): Show | 20 | HG00280.hp1 HG00639.hp1 HG01109.hp1 others(17): Show |
intron_variant | MODIFIER | c.99+924dupT | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr14 | 51690850 | |||||
chr14:51690971
|
A | G | 102 | a0001c0002t0001g0166a0001c0002t0001g0196a0001c0003t0001g0006others(99): Show | 122 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(119): Show |
intron_variant | MODIFIER | c.99+1036A>G | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 2/13 | chr14 | 51690971 | ||||||
chr14:51691065
|
T | A | 2 | a0001c0003t0001g0194a0003c0010t0001g0071 | 2 | HG03139.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.99+1130T>A | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 2/13 | chr14 | 51691065 | ||||||
chr14:51691118
|
A | G | 1 | a0001c0001t0024g0124 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.99+1183A>G | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 2/13 | chr14 | 51691118 | ||||||
chr14:51691187
|
A | G | 206 | a0001c0001t0001g0113a0001c0001t0001g0164a0001c0001t0001g0168others(203): Show | 255 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(252): Show |
intron_variant | MODIFIER | c.99+1252A>G | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 2/13 | chr14 | 51691187 | ||||||
chr14:51691270
|
T | C | 4 | a0001c0004t0001g0140a0001c0004t0001g0141a0001c0004t0001g0207others(1): Show | 4 | HG02723.hp2 HG03098.hp1 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.99+1335T>C | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 2/13 | chr14 | 51691270 | ||||||
chr14:51691352
|
A | G | 2 | a0002c0008t0009g0072a0002c0008t0009g0291 | 2 | HG02258.hp2 HG02572.hp2 |
intron_variant | MODIFIER | c.99+1417A>G | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 2/13 | chr14 | 51691352 | ||||||
chr14:51691380
|
G | A | 1 | a0001c0006t0003g0153 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.99+1445G>A | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 2/13 | chr14 | 51691380 | ||||||
chr14:51691451
|
C | T | 4 | a0001c0001t0002g0003a0001c0001t0002g0117a0001c0001t0002g0118others(1): Show | 8 | NA18954.hp2 NA18957.hp1 NA18973.hp1 others(5): Show |
intron_variant | MODIFIER | c.99+1516C>T | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 2/13 | chr14 | 51691451 | ||||||
chr14:51691585
|
TTGA | T | 56 | a0001c0003t0001g0006a0001c0003t0001g0011a0001c0003t0001g0014others(53): Show | 73 | HG00140.hp1 HG00323.hp1 HG00438.hp1 others(70): Show |
intron_variant | MODIFIER | c.99+1652_99+1654del others(3): Show |
FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr14 | 51691585 | |||||
chr14:51691586
|
TGA | T | 16 | a0001c0003t0001g0018a0001c0003t0001g0041a0001c0003t0001g0100others(13): Show | 19 | HG00544.hp2 HG01175.hp1 HG02056.hp2 others(16): Show |
intron_variant | MODIFIER | c.99+1652_99+1653del others(2): Show |
FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 2/13 | chr14 | 51691586 | ||||||
chr14:51691588
|
A | AT | 13 | a0001c0002t0001g0089a0001c0002t0001g0093a0001c0002t0001g0179others(10): Show | 13 | HG01175.hp2 HG01243.hp2 HG02165.hp2 others(10): Show |
intron_variant | MODIFIER | c.99+1677dupT | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr14 | 51691588 | |||||
chr14:51691588
|
A | T | 1 | a0001c0003t0001g0212 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.99+1653A>T | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 2/13 | chr14 | 51691588 | ||||||
chr14:51691588
|
AT | A | 11 | a0001c0002t0001g0092a0001c0002t0001g0127a0001c0002t0001g0176others(8): Show | 12 | HG00099.hp1 HG00639.hp1 HG01109.hp1 others(9): Show |
intron_variant | MODIFIER | c.99+1677delT | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr14 | 51691588 | |||||
chr14:51691588
|
ATT | A | 10 | a0001c0004t0005g0185a0001c0004t0005g0190a0001c0004t0005g0292others(7): Show | 11 | HG01358.hp1 HG01433.hp1 HG02280.hp2 others(8): Show |
intron_variant | MODIFIER | c.99+1676_99+1677del others(2): Show |
FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr14 | 51691588 | |||||
chr14:51691588
|
ATTT | A | 9 | a0001c0001t0007g0159a0001c0004t0001g0140a0001c0004t0001g0141others(6): Show | 9 | HG01109.hp2 HG02083.hp2 HG02258.hp2 others(6): Show |
intron_variant | MODIFIER | c.99+1675_99+1677del others(3): Show |
FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr14 | 51691588 | |||||
chr14:51691588
|
ATTTT | A | 8 | a0001c0001t0002g0061a0001c0001t0002g0160a0001c0001t0002g0161others(5): Show | 8 | HG00733.hp2 HG01261.hp2 HG02165.hp1 others(5): Show |
intron_variant | MODIFIER | c.99+1674_99+1677del others(4): Show |
FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr14 | 51691588 | |||||
chr14:51691588
|
ATTTTT | A | 91 | a0001c0001t0001g0113a0001c0001t0001g0164a0001c0001t0001g0168others(88): Show | 117 | HG00099.hp2 HG00140.hp2 HG00323.hp2 others(114): Show |
intron_variant | MODIFIER | c.99+1673_99+1677del others(5): Show |
FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr14 | 51691588 | |||||
chr14:51691828
|
C | T | 102 | a0001c0001t0001g0113a0001c0001t0001g0164a0001c0001t0001g0168others(99): Show | 128 | HG00099.hp2 HG00140.hp2 HG00323.hp2 others(125): Show |
intron_variant | MODIFIER | c.99+1893C>T | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 2/13 | chr14 | 51691828 | ||||||
chr14:51691843
|
C | T | 10 | a0001c0001t0001g0113a0001c0001t0002g0054a0001c0001t0002g0114others(7): Show | 10 | HG01891.hp1 HG02486.hp1 HG02717.hp1 others(7): Show |
intron_variant | MODIFIER | c.99+1908C>T | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 2/13 | chr14 | 51691843 | ||||||
chr14:51691875
|
G | A | 1 | a0001c0001t0001g0113 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.99+1940G>A | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 2/13 | chr14 | 51691875 | ||||||
chr14:51691955
|
A | AAT | 190 | a0001c0001t0001g0113a0001c0001t0001g0164a0001c0001t0001g0168others(187): Show | 236 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(233): Show |
intron_variant | MODIFIER | c.99+2025_99+2026dup others(2): Show |
FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr14 | 51691955 | |||||
chr14:51691958
|
A | T | 1 | a0001c0004t0001g0035 | 2 | HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.99+2023A>T | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 2/13 | chr14 | 51691958 | ||||||
chr14:51692111
|
A | G | 1 | a0001c0002t0001g0174 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.99+2176A>G | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 2/13 | chr14 | 51692111 | ||||||
chr14:51692115
|
G | T | 3 | a0001c0001t0002g0049a0001c0001t0002g0050a0001c0001t0002g0051 | 3 | HG01256.hp1 HG01515.hp2 HG01517.hp1 |
intron_variant | MODIFIER | c.99+2180G>T | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 2/13 | chr14 | 51692115 | ||||||
chr14:51692228
|
ATT | A | 4 | a0001c0004t0005g0185a0001c0004t0005g0187a0001c0004t0005g0190others(1): Show | 4 | HG02083.hp2 NA18994.hp2 NA19055.hp1 others(1): Show |
intron_variant | MODIFIER | c.99+2296_99+2297del others(2): Show |
FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr14 | 51692228 | |||||
chr14:51692305
|
A | G | 4 | a0001c0004t0005g0185a0001c0004t0005g0187a0001c0004t0005g0190others(1): Show | 4 | HG02083.hp2 NA18994.hp2 NA19055.hp1 others(1): Show |
intron_variant | MODIFIER | c.99+2370A>G | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 2/13 | chr14 | 51692305 | ||||||
chr14:51692355
|
T | C | 1 | a0001c0001t0002g0311 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.99+2420T>C | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 2/13 | chr14 | 51692355 | ||||||
chr14:51692420
|
A | G | 3 | a0001c0002t0001g0088a0001c0002t0001g0092a0001c0002t0001g0093 | 3 | NA18972.hp1 NA18986.hp2 NA19001.hp1 |
intron_variant | MODIFIER | c.99+2485A>G | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 2/13 | chr14 | 51692420 | ||||||
chr14:51692472
|
A | ATG | 134 | a0001c0001t0002g0047a0001c0001t0002g0048a0001c0001t0002g0049others(131): Show | 160 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(157): Show |
intron_variant | MODIFIER | c.99+2559_99+2560dup others(2): Show |
FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr14 | 51692472 | |||||
chr14:51692472
|
A | ATGTG | 85 | a0001c0001t0001g0113a0001c0001t0001g0164a0001c0001t0001g0202others(82): Show | 111 | HG00099.hp2 HG00140.hp2 HG00323.hp2 others(108): Show |
intron_variant | MODIFIER | c.99+2557_99+2560dup others(4): Show |
FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr14 | 51692472 | |||||
chr14:51692472
|
A | ATGTGTG | 7 | a0001c0001t0001g0168a0001c0001t0002g0082a0001c0001t0002g0115others(4): Show | 7 | HG00544.hp1 HG02135.hp1 HG03225.hp2 others(4): Show |
intron_variant | MODIFIER | c.99+2555_99+2560dup others(6): Show |
FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr14 | 51692472 | |||||
chr14:51692472
|
ATG | A | 78 | a0001c0003t0001g0006a0001c0003t0001g0011a0001c0003t0001g0014others(75): Show | 97 | HG00140.hp1 HG00323.hp1 HG00438.hp1 others(94): Show |
intron_variant | MODIFIER | c.99+2559_99+2560del others(2): Show |
FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr14 | 51692472 | |||||
chr14:51692482
|
G | GTA | 7 | a0001c0002t0001g0028a0001c0002t0001g0184a0001c0002t0001g0186others(4): Show | 8 | HG00738.hp2 HG00741.hp1 HG01099.hp1 others(5): Show |
intron_variant | MODIFIER | c.99+2548_99+2549ins others(2): Show |
FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr14 | 51692482 | |||||
chr14:51692510
|
G | T | 1 | a0001c0002t0001g0137 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.99+2575G>T | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 2/13 | chr14 | 51692510 | ||||||
chr14:51692854
|
A | G | 1 | a0001c0003t0001g0268 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.99+2919A>G | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 2/13 | chr14 | 51692854 | ||||||
chr14:51692871
|
A | T | 2 | a0002c0008t0009g0072a0002c0008t0009g0291 | 2 | HG02258.hp2 HG02572.hp2 |
intron_variant | MODIFIER | c.99+2936A>T | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 2/13 | chr14 | 51692871 | ||||||
chr14:51692878
|
C | G | 110 | a0001c0001t0001g0113a0001c0001t0001g0164a0001c0001t0001g0168others(107): Show | 136 | HG00099.hp2 HG00140.hp2 HG00323.hp2 others(133): Show |
intron_variant | MODIFIER | c.99+2943C>G | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 2/13 | chr14 | 51692878 | ||||||
chr14:51692965
|
A | G | 4 | a0001c0004t0001g0140a0001c0004t0001g0141a0001c0004t0001g0207others(1): Show | 4 | HG02723.hp2 HG03098.hp1 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.99+3030A>G | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 2/13 | chr14 | 51692965 | ||||||
chr14:51692987
|
C | G | 4 | a0001c0004t0005g0185a0001c0004t0005g0187a0001c0004t0005g0190others(1): Show | 4 | HG02083.hp2 NA18994.hp2 NA19055.hp1 others(1): Show |
intron_variant | MODIFIER | c.99+3052C>G | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 2/13 | chr14 | 51692987 | ||||||
chr14:51693025
|
G | T | 1 | a0001c0003t0001g0212 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.99+3090G>T | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 2/13 | chr14 | 51693025 | ||||||
chr14:51693036
|
T | A | 1 | a0001c0003t0001g0275 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.99+3101T>A | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 2/13 | chr14 | 51693036 | ||||||
chr14:51693211
|
G | A | 1 | a0001c0006t0003g0154 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.99+3276G>A | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 2/13 | chr14 | 51693211 | ||||||
chr14:51693354
|
G | A | 4 | a0001c0004t0001g0140a0001c0004t0001g0141a0001c0004t0001g0207others(1): Show | 4 | HG02723.hp2 HG03098.hp1 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.99+3419G>A | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 2/13 | chr14 | 51693354 | ||||||
chr14:51693391
|
A | G | 2 | a0001c0004t0005g0185a0001c0004t0005g0190 | 2 | NA18994.hp2 NA19082.hp2 |
intron_variant | MODIFIER | c.99+3456A>G | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 2/13 | chr14 | 51693391 | ||||||
chr14:51693453
|
G | A | 1 | a0001c0002t0001g0234 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.99+3518G>A | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 2/13 | chr14 | 51693453 | ||||||
chr14:51693476
|
C | G | 4 | a0001c0004t0001g0140a0001c0004t0001g0141a0001c0004t0001g0207others(1): Show | 4 | HG02723.hp2 HG03098.hp1 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.99+3541C>G | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 2/13 | chr14 | 51693476 | ||||||
chr14:51693521
|
T | C | 5 | a0001c0002t0001g0234a0001c0002t0004g0038a0001c0002t0004g0222others(2): Show | 6 | HG00280.hp2 HG00733.hp1 HG01069.hp2 others(3): Show |
intron_variant | MODIFIER | c.99+3586T>C | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 2/13 | chr14 | 51693521 | ||||||
chr14:51693622
|
T | TG | 314 | a0001c0001t0001g0113a0001c0001t0001g0164a0001c0001t0001g0168others(311): Show | 386 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(383): Show |
intron_variant | MODIFIER | c.99+3688dupG | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr14 | 51693622 | |||||
chr14:51693704
|
G | T | 79 | a0001c0003t0001g0006a0001c0003t0001g0011a0001c0003t0001g0014others(76): Show | 99 | HG00140.hp1 HG00323.hp1 HG00438.hp1 others(96): Show |
intron_variant | MODIFIER | c.99+3769G>T | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 2/13 | chr14 | 51693704 | ||||||
chr14:51693889
|
C | T | 1 | a0001c0004t0016g0070 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.99+3954C>T | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 2/13 | chr14 | 51693889 | ||||||
chr14:51693933
|
A | G | 4 | a0001c0004t0005g0185a0001c0004t0005g0187a0001c0004t0005g0190others(1): Show | 4 | HG02083.hp2 NA18994.hp2 NA19055.hp1 others(1): Show |
intron_variant | MODIFIER | c.99+3998A>G | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 2/13 | chr14 | 51693933 | ||||||
chr14:51693976
|
G | A | 11 | a0001c0006t0003g0027a0001c0006t0003g0073a0001c0006t0003g0151others(8): Show | 12 | HG01358.hp1 HG01433.hp1 HG02145.hp2 others(9): Show |
intron_variant | MODIFIER | c.99+4041G>A | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 2/13 | chr14 | 51693976 | ||||||
chr14:51694120
|
A | T | 2 | a0001c0001t0001g0202a0001c0001t0001g0209 | 2 | HG02451.hp1 HG02572.hp1 |
intron_variant | MODIFIER | c.100-4022A>T | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 2/13 | chr14 | 51694120 | ||||||
chr14:51694280
|
G | A | 4 | a0001c0004t0005g0185a0001c0004t0005g0187a0001c0004t0005g0190others(1): Show | 4 | HG02083.hp2 NA18994.hp2 NA19055.hp1 others(1): Show |
intron_variant | MODIFIER | c.100-3862G>A | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 2/13 | chr14 | 51694280 | ||||||
chr14:51694303
|
T | C | 193 | a0001c0001t0001g0113a0001c0001t0001g0164a0001c0001t0001g0168others(190): Show | 240 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(237): Show |
intron_variant | MODIFIER | c.100-3839T>C | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 2/13 | chr14 | 51694303 | ||||||
chr14:51694415
|
T | A | 103 | a0001c0001t0001g0113a0001c0001t0001g0164a0001c0001t0001g0168others(100): Show | 129 | HG00099.hp2 HG00140.hp2 HG00323.hp2 others(126): Show |
intron_variant | MODIFIER | c.100-3727T>A | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 2/13 | chr14 | 51694415 | ||||||
chr14:51694719
|
T | C | 1 | a0001c0001t0002g0128 | 1 | NA18988.hp2 | intron_variant | MODIFIER | c.100-3423T>C | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 2/13 | chr14 | 51694719 | ||||||
chr14:51694910
|
CCATGGCC others(267): Show |
C | 4 | a0001c0004t0001g0140a0001c0004t0001g0141a0001c0004t0001g0207others(1): Show | 4 | HG02723.hp2 HG03098.hp1 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.100-3229_100-2956d others(2): Show |
FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr14 | 51694910 | |||||
chr14:51694968
|
A | G | 3 | a0001c0001t0006g0019a0001c0001t0006g0059a0001c0001t0023g0058 | 4 | HG01261.hp1 HG02965.hp2 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.100-3174A>G | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 2/13 | chr14 | 51694968 | ||||||
chr14:51694978
|
A | G | 82 | a0001c0002t0001g0166a0001c0003t0001g0006a0001c0003t0001g0011others(79): Show | 103 | HG00140.hp1 HG00323.hp1 HG00438.hp1 others(100): Show |
intron_variant | MODIFIER | c.100-3164A>G | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 2/13 | chr14 | 51694978 | ||||||
chr14:51694982
|
G | A | 4 | a0001c0004t0005g0185a0001c0004t0005g0187a0001c0004t0005g0190others(1): Show | 4 | HG02083.hp2 NA18994.hp2 NA19055.hp1 others(1): Show |
intron_variant | MODIFIER | c.100-3160G>A | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 2/13 | chr14 | 51694982 | ||||||
chr14:51695069
|
C | CAGTCACA others(4): Show |
1 | a0001c0002t0001g0091 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.100-3072_100-3062d others(13): Show |
FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr14 | 51695069 | |||||
chr14:51695085
|
A | C | 1 | a0001c0003t0001g0261 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.100-3057A>C | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 2/13 | chr14 | 51695085 | ||||||
chr14:51695170
|
G | A | 4 | a0001c0004t0005g0185a0001c0004t0005g0187a0001c0004t0005g0190others(1): Show | 4 | HG02083.hp2 NA18994.hp2 NA19055.hp1 others(1): Show |
intron_variant | MODIFIER | c.100-2972G>A | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 2/13 | chr14 | 51695170 | ||||||
chr14:51695224
|
T | A | 4 | a0001c0001t0002g0023a0001c0001t0002g0104a0001c0001t0002g0105others(1): Show | 5 | HG02132.hp1 NA18949.hp1 NA18970.hp1 others(2): Show |
intron_variant | MODIFIER | c.100-2918T>A | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 2/13 | chr14 | 51695224 | ||||||
chr14:51695374
|
G | A | 213 | a0001c0001t0001g0113a0001c0001t0001g0164a0001c0001t0001g0168others(210): Show | 261 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(258): Show |
intron_variant | MODIFIER | c.100-2768G>A | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 2/13 | chr14 | 51695374 | ||||||
chr14:51695387
|
C | A | 2 | a0001c0002t0014g0243a0001c0002t0015g0240 | 2 | HG01496.hp1 HG03491.hp1 |
intron_variant | MODIFIER | c.100-2755C>A | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 2/13 | chr14 | 51695387 | ||||||
chr14:51695647
|
C | G | 190 | a0001c0001t0001g0113a0001c0001t0001g0164a0001c0001t0001g0168others(187): Show | 236 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(233): Show |
intron_variant | MODIFIER | c.100-2495C>G | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 2/13 | chr14 | 51695647 | ||||||
chr14:51695841
|
C | T | 1 | a0001c0001t0002g0156 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.100-2301C>T | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 2/13 | chr14 | 51695841 | ||||||
chr14:51696315
|
C | T | 4 | a0001c0004t0005g0185a0001c0004t0005g0187a0001c0004t0005g0190others(1): Show | 4 | HG02083.hp2 NA18994.hp2 NA19055.hp1 others(1): Show |
intron_variant | MODIFIER | c.100-1827C>T | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 2/13 | chr14 | 51696315 | ||||||
chr14:51696431
|
A | G | 4 | a0001c0004t0005g0185a0001c0004t0005g0187a0001c0004t0005g0190others(1): Show | 4 | HG02083.hp2 NA18994.hp2 NA19055.hp1 others(1): Show |
intron_variant | MODIFIER | c.100-1711A>G | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 2/13 | chr14 | 51696431 | ||||||
chr14:51696542
|
G | C | 1 | a0005c0016t0002g0106 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.100-1600G>C | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 2/13 | chr14 | 51696542 | ||||||
chr14:51696637
|
C | G | 4 | a0001c0004t0005g0185a0001c0004t0005g0187a0001c0004t0005g0190others(1): Show | 4 | HG02083.hp2 NA18994.hp2 NA19055.hp1 others(1): Show |
intron_variant | MODIFIER | c.100-1505C>G | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 2/13 | chr14 | 51696637 | ||||||
chr14:51696728
|
C | T | 3 | a0001c0001t0002g0147a0001c0001t0002g0148a0001c0001t0021g0218 | 3 | HG02886.hp2 HG02922.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.100-1414C>T | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 2/13 | chr14 | 51696728 | ||||||
chr14:51696751
|
C | CA | 187 | a0001c0001t0001g0113a0001c0001t0001g0164a0001c0001t0001g0168others(184): Show | 234 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(231): Show |
intron_variant | MODIFIER | c.100-1377dupA | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr14 | 51696751 | |||||
chr14:51696765
|
A | AT | 8 | a0001c0002t0001g0031a0001c0002t0001g0032a0001c0002t0001g0033others(5): Show | 11 | HG00099.hp1 HG00741.hp2 HG01070.hp1 others(8): Show |
intron_variant | MODIFIER | c.100-1377_100-1376i others(3): Show |
FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 2/13 | chr14 | 51696765 | ||||||
chr14:51696790
|
A | C | 5 | a0001c0002t0001g0234a0001c0002t0004g0038a0001c0002t0004g0222others(2): Show | 6 | HG00280.hp2 HG00733.hp1 HG01069.hp2 others(3): Show |
intron_variant | MODIFIER | c.100-1352A>C | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 2/13 | chr14 | 51696790 | ||||||
chr14:51696845
|
A | G | 4 | a0001c0004t0005g0185a0001c0004t0005g0187a0001c0004t0005g0190others(1): Show | 4 | HG02083.hp2 NA18994.hp2 NA19055.hp1 others(1): Show |
intron_variant | MODIFIER | c.100-1297A>G | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 2/13 | chr14 | 51696845 | ||||||
chr14:51696866
|
G | A | 216 | a0001c0001t0001g0113a0001c0001t0001g0164a0001c0001t0001g0168others(213): Show | 265 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(262): Show |
intron_variant | MODIFIER | c.100-1276G>A | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 2/13 | chr14 | 51696866 | ||||||
chr14:51696871
|
C | T | 1 | a0001c0003t0001g0266 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.100-1271C>T | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 2/13 | chr14 | 51696871 | ||||||
chr14:51697086
|
A | G | 1 | a0001c0002t0001g0193 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.100-1056A>G | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 2/13 | chr14 | 51697086 | ||||||
chr14:51697332
|
C | T | 64 | a0001c0001t0001g0164a0001c0001t0001g0168a0001c0001t0002g0001others(61): Show | 86 | HG00140.hp2 HG00323.hp2 HG00544.hp1 others(83): Show |
intron_variant | MODIFIER | c.100-810C>T | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 2/13 | chr14 | 51697332 | ||||||
chr14:51697409
|
G | A | 4 | a0001c0004t0001g0140a0001c0004t0001g0141a0001c0004t0001g0207others(1): Show | 4 | HG02723.hp2 HG03098.hp1 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.100-733G>A | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 2/13 | chr14 | 51697409 | ||||||
chr14:51697710
|
A | G | 1 | a0001c0002t0001g0091 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.100-432A>G | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 2/13 | chr14 | 51697710 | ||||||
chr14:51697791
|
A | T | 9 | a0001c0004t0001g0046a0001c0004t0001g0063a0001c0004t0001g0064others(6): Show | 9 | HG00280.hp1 HG00639.hp1 HG01109.hp1 others(6): Show |
intron_variant | MODIFIER | c.100-351A>T | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 2/13 | chr14 | 51697791 | ||||||
chr14:51697831
|
G | A | 1 | a0001c0001t0002g0037 | 2 | HG01256.hp2 HG01258.hp2 |
intron_variant | MODIFIER | c.100-311G>A | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 2/13 | chr14 | 51697831 | ||||||
chr14:51698060
|
G | A | 9 | a0001c0001t0002g0047a0001c0001t0002g0143a0001c0001t0002g0144others(6): Show | 9 | HG01891.hp2 HG02109.hp1 HG02280.hp1 others(6): Show |
intron_variant | MODIFIER | c.100-82G>A | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 2/13 | chr14 | 51698060 | ||||||
chr14:51698351
|
GGACT | G | 4 | a0001c0004t0001g0140a0001c0004t0001g0141a0001c0004t0001g0207others(1): Show | 4 | HG02723.hp2 HG03098.hp1 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.190+122_190+125del others(4): Show |
FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr14 | 51698351 | |||||
chr14:51698365
|
T | G | 184 | a0001c0001t0001g0113a0001c0001t0001g0164a0001c0001t0001g0168others(181): Show | 231 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(228): Show |
intron_variant | MODIFIER | c.190+133T>G | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 3/13 | chr14 | 51698365 | ||||||
chr14:51698408
|
A | G | 203 | a0001c0001t0001g0113a0001c0001t0001g0164a0001c0001t0001g0168others(200): Show | 251 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(248): Show |
intron_variant | MODIFIER | c.190+176A>G | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 3/13 | chr14 | 51698408 | ||||||
chr14:51698461
|
C | G | 4 | a0001c0004t0001g0140a0001c0004t0001g0141a0001c0004t0001g0207others(1): Show | 4 | HG02723.hp2 HG03098.hp1 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.190+229C>G | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 3/13 | chr14 | 51698461 | ||||||
chr14:51698615
|
A | C | 8 | a0001c0002t0001g0031a0001c0002t0001g0032a0001c0002t0001g0033others(5): Show | 11 | HG00099.hp1 HG00741.hp2 HG01070.hp1 others(8): Show |
intron_variant | MODIFIER | c.190+383A>C | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 3/13 | chr14 | 51698615 | ||||||
chr14:51698703
|
C | T | 1 | a0001c0004t0001g0068 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.190+471C>T | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 3/13 | chr14 | 51698703 | ||||||
chr14:51698704
|
G | T | 205 | a0001c0001t0001g0113a0001c0001t0001g0164a0001c0001t0001g0168others(202): Show | 253 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(250): Show |
intron_variant | MODIFIER | c.190+472G>T | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 3/13 | chr14 | 51698704 | ||||||
chr14:51698735
|
A | T | 82 | a0001c0002t0001g0166a0001c0003t0001g0006a0001c0003t0001g0011others(79): Show | 103 | HG00140.hp1 HG00323.hp1 HG00438.hp1 others(100): Show |
intron_variant | MODIFIER | c.190+503A>T | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 3/13 | chr14 | 51698735 | ||||||
chr14:51698791
|
T | A | 4 | a0001c0004t0001g0140a0001c0004t0001g0141a0001c0004t0001g0207others(1): Show | 4 | HG02723.hp2 HG03098.hp1 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.190+559T>A | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 3/13 | chr14 | 51698791 | ||||||
chr14:51698829
|
C | A | 1 | a0001c0002t0001g0173 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.190+597C>A | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 3/13 | chr14 | 51698829 | ||||||
chr14:51698898
|
G | A | 1 | a0001c0004t0012g0182 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.190+666G>A | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 3/13 | chr14 | 51698898 | ||||||
chr14:51698932
|
A | G | 1 | a0001c0002t0001g0136 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.190+700A>G | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 3/13 | chr14 | 51698932 | ||||||
chr14:51699001
|
G | A | 2 | a0001c0001t0002g0012a0004c0012t0002g0210 | 4 | HG02809.hp1 HG03041.hp2 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.190+769G>A | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 3/13 | chr14 | 51699001 | ||||||
chr14:51699010
|
T | C | 4 | a0001c0004t0001g0140a0001c0004t0001g0141a0001c0004t0001g0207others(1): Show | 4 | HG02723.hp2 HG03098.hp1 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.190+778T>C | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 3/13 | chr14 | 51699010 | ||||||
chr14:51699364
|
A | G | 1 | a0001c0002t0013g0052 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.190+1132A>G | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 3/13 | chr14 | 51699364 | ||||||
chr14:51699534
|
C | T | 8 | a0001c0004t0001g0046a0001c0004t0001g0063a0001c0004t0001g0064others(5): Show | 8 | HG00280.hp1 HG00639.hp1 HG01109.hp1 others(5): Show |
intron_variant | MODIFIER | c.190+1302C>T | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 3/13 | chr14 | 51699534 | ||||||
chr14:51699571
|
C | G | 2 | a0001c0001t0002g0146a0001c0003t0001g0212 | 2 | HG02280.hp1 HG02615.hp2 |
intron_variant | MODIFIER | c.190+1339C>G | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 3/13 | chr14 | 51699571 | ||||||
chr14:51699608
|
T | C | 1 | a0001c0006t0003g0153 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.190+1376T>C | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 3/13 | chr14 | 51699608 | ||||||
chr14:51699627
|
G | A | 1 | a0001c0002t0002g0204 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.190+1395G>A | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 3/13 | chr14 | 51699627 | ||||||
chr14:51699701
|
C | G | 2 | a0001c0002t0001g0205a0001c0002t0001g0219 | 2 | HG01516.hp2 HG01981.hp1 |
intron_variant | MODIFIER | c.191-1355C>G | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 3/13 | chr14 | 51699701 | ||||||
chr14:51699836
|
C | G | 1 | a0001c0003t0001g0278 | 1 | NA18988.hp1 | intron_variant | MODIFIER | c.191-1220C>G | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 3/13 | chr14 | 51699836 | ||||||
chr14:51699837
|
G | A | 15 | a0001c0004t0005g0185a0001c0004t0005g0187a0001c0004t0005g0190others(12): Show | 16 | HG01358.hp1 HG01433.hp1 HG02083.hp2 others(13): Show |
intron_variant | MODIFIER | c.191-1219G>A | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 3/13 | chr14 | 51699837 | ||||||
chr14:51699927
|
TAAG | T | 4 | a0001c0003t0001g0044a0001c0003t0001g0258a0001c0003t0001g0273others(1): Show | 5 | HG00544.hp2 HG02155.hp1 NA18747.hp2 others(2): Show |
intron_variant | MODIFIER | c.191-1128_191-1126d others(5): Show |
FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 3/13 | chr14 | 51699927 | ||||||
chr14:51699939
|
C | CT | 103 | a0001c0001t0001g0113a0001c0001t0001g0164a0001c0001t0001g0168others(100): Show | 129 | HG00099.hp2 HG00140.hp2 HG00323.hp2 others(126): Show |
intron_variant | MODIFIER | c.191-1110dupT | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr14 | 51699939 | |||||
chr14:51699956
|
A | T | 2 | a0002c0008t0009g0072a0002c0008t0009g0291 | 2 | HG02258.hp2 HG02572.hp2 |
intron_variant | MODIFIER | c.191-1100A>T | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 3/13 | chr14 | 51699956 | ||||||
chr14:51699995
|
A | G | 1 | a0001c0002t0001g0090 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.191-1061A>G | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 3/13 | chr14 | 51699995 | ||||||
chr14:51700011
|
A | G | 4 | a0001c0004t0001g0140a0001c0004t0001g0141a0001c0004t0001g0207others(1): Show | 4 | HG02723.hp2 HG03098.hp1 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.191-1045A>G | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 3/13 | chr14 | 51700011 | ||||||
chr14:51700024
|
C | T | 103 | a0001c0001t0001g0113a0001c0001t0001g0164a0001c0001t0001g0168others(100): Show | 129 | HG00099.hp2 HG00140.hp2 HG00323.hp2 others(126): Show |
intron_variant | MODIFIER | c.191-1032C>T | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 3/13 | chr14 | 51700024 | ||||||
chr14:51700102
|
C | T | 103 | a0001c0001t0001g0113a0001c0001t0001g0164a0001c0001t0001g0168others(100): Show | 129 | HG00099.hp2 HG00140.hp2 HG00323.hp2 others(126): Show |
intron_variant | MODIFIER | c.191-954C>T | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 3/13 | chr14 | 51700102 | ||||||
chr14:51700105
|
C | T | 1 | a0001c0002t0001g0087 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.191-951C>T | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 3/13 | chr14 | 51700105 | ||||||
chr14:51700402
|
G | C | 1 | a0001c0004t0012g0182 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.191-654G>C | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 3/13 | chr14 | 51700402 | ||||||
chr14:51700687
|
C | T | 1 | a0001c0001t0002g0306 | 1 | NA19054.hp1 | intron_variant | MODIFIER | c.191-369C>T | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 3/13 | chr14 | 51700687 | ||||||
chr14:51700960
|
G | A | 1 | a0001c0004t0005g0185 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.191-96G>A | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 3/13 | chr14 | 51700960 | ||||||
chr14:51700983
|
T | C | 2 | a0001c0004t0001g0035a0001c0004t0016g0070 | 3 | HG02818.hp2 HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.191-73T>C | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 3/13 | chr14 | 51700983 | ||||||
chr14:51701191
|
GA | G | 11 | a0001c0006t0003g0027a0001c0006t0003g0073a0001c0006t0003g0151others(8): Show | 12 | HG01358.hp1 HG01433.hp1 HG02145.hp2 others(9): Show |
intron_variant | MODIFIER | c.294+33delA | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 4/13 | chr14 | 51701191 | ||||||
chr14:51701200
|
T | A | 12 | a0001c0001t0002g0024a0001c0001t0007g0096a0001c0002t0001g0196others(9): Show | 13 | HG00280.hp1 HG00639.hp1 HG00733.hp2 others(10): Show |
intron_variant | MODIFIER | c.294+41T>A | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 4/13 | chr14 | 51701200 | ||||||
chr14:51701312
|
G | GTA | 4 | a0001c0002t0001g0134a0001c0003t0001g0308a0001c0003t0001g0309others(1): Show | 4 | HG02015.hp2 HG03139.hp1 NA18981.hp1 others(1): Show |
intron_variant | MODIFIER | c.294+166_294+167dup others(2): Show |
FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr14 | 51701312 | |||||
chr14:51701343
|
ATTTTC | A | 102 | a0001c0001t0001g0113a0001c0001t0001g0164a0001c0001t0001g0168others(99): Show | 128 | HG00099.hp2 HG00140.hp2 HG00544.hp1 others(125): Show |
intron_variant | MODIFIER | c.294+190_294+194del others(5): Show |
FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr14 | 51701343 | |||||
chr14:51701372
|
G | GAGTATAT others(20): Show |
4 | a0001c0004t0005g0185a0001c0004t0005g0187a0001c0004t0005g0190others(1): Show | 4 | HG02083.hp2 NA18994.hp2 NA19055.hp1 others(1): Show |
intron_variant | MODIFIER | c.294+226_294+252dup others(27): Show |
FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr14 | 51701372 | |||||
chr14:51701403
|
A | G | 2 | a0002c0008t0009g0072a0002c0008t0009g0291 | 2 | HG02258.hp2 HG02572.hp2 |
intron_variant | MODIFIER | c.294+244A>G | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 4/13 | chr14 | 51701403 | ||||||
chr14:51701472
|
GTA | G | 3 | a0001c0003t0001g0194a0001c0004t0016g0070a0003c0010t0001g0071 | 3 | HG02818.hp2 HG03139.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.294+326_294+327del others(2): Show |
FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chr14 | 51701472 | |||||
chr14:51701597
|
A | G | 4 | a0001c0004t0005g0185a0001c0004t0005g0187a0001c0004t0005g0190others(1): Show | 4 | HG02083.hp2 NA18994.hp2 NA19055.hp1 others(1): Show |
intron_variant | MODIFIER | c.294+438A>G | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 4/13 | chr14 | 51701597 | ||||||
chr14:51701621
|
G | A | 2 | a0001c0001t0011g0131a0001c0001t0011g0132 | 2 | HG02896.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.294+462G>A | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 4/13 | chr14 | 51701621 | ||||||
chr14:51701916
|
A | C | 2 | a0001c0004t0001g0035a0001c0004t0016g0070 | 3 | HG02818.hp2 HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.295-596A>C | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 4/13 | chr14 | 51701916 | ||||||
chr14:51702092
|
A | G | 184 | a0001c0001t0001g0113a0001c0001t0001g0164a0001c0001t0001g0168others(181): Show | 231 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(228): Show |
intron_variant | MODIFIER | c.295-420A>G | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 4/13 | chr14 | 51702092 | ||||||
chr14:51702123
|
T | C | 4 | a0001c0004t0001g0140a0001c0004t0001g0141a0001c0004t0001g0207others(1): Show | 4 | HG02723.hp2 HG03098.hp1 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.295-389T>C | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 4/13 | chr14 | 51702123 | ||||||
chr14:51702170
|
T | C | 1 | a0001c0004t0001g0056 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.295-342T>C | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 4/13 | chr14 | 51702170 | ||||||
chr14:51702301
|
T | C | 2 | a0002c0008t0009g0072a0002c0008t0009g0291 | 2 | HG02258.hp2 HG02572.hp2 |
intron_variant | MODIFIER | c.295-211T>C | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 4/13 | chr14 | 51702301 | ||||||
chr14:51702373
|
G | A | 104 | a0001c0001t0001g0113a0001c0001t0001g0164a0001c0001t0001g0168others(101): Show | 131 | HG00099.hp2 HG00140.hp2 HG00544.hp1 others(128): Show |
intron_variant | MODIFIER | c.295-139G>A | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 4/13 | chr14 | 51702373 | ||||||
chr14:51702623
|
T | G | 4 | a0001c0004t0005g0185a0001c0004t0005g0187a0001c0004t0005g0190others(1): Show | 4 | HG02083.hp2 NA18994.hp2 NA19055.hp1 others(1): Show |
intron_variant | MODIFIER | c.371+35T>G | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 5/13 | chr14 | 51702623 | ||||||
chr14:51702847
|
A | G | 1 | a0001c0003t0001g0076 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.371+259A>G | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 5/13 | chr14 | 51702847 | ||||||
chr14:51702955
|
T | A | 2 | a0001c0001t0002g0080a0001c0001t0002g0112 | 2 | HG00597.hp1 NA19006.hp2 |
intron_variant | MODIFIER | c.371+367T>A | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 5/13 | chr14 | 51702955 | ||||||
chr14:51702988
|
G | C | 1 | a0001c0001t0002g0155 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.371+400G>C | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 5/13 | chr14 | 51702988 | ||||||
chr14:51703029
|
G | T | 72 | a0001c0003t0001g0006a0001c0003t0001g0011a0001c0003t0001g0014others(69): Show | 92 | HG00140.hp1 HG00323.hp1 HG00438.hp1 others(89): Show |
intron_variant | MODIFIER | c.371+441G>T | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 5/13 | chr14 | 51703029 | ||||||
chr14:51703085
|
A | G | 1 | a0001c0001t0007g0096 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.371+497A>G | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 5/13 | chr14 | 51703085 | ||||||
chr14:51703134
|
C | A | 1 | a0001c0001t0002g0149 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.371+546C>A | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 5/13 | chr14 | 51703134 | ||||||
chr14:51703154
|
G | A | 1 | a0001c0001t0002g0051 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.371+566G>A | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 5/13 | chr14 | 51703154 | ||||||
chr14:51703399
|
A | G | 2 | a0001c0004t0001g0035a0001c0004t0016g0070 | 3 | HG02818.hp2 HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.371+811A>G | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 5/13 | chr14 | 51703399 | ||||||
chr14:51703481
|
A | T | 1 | a0001c0004t0005g0292 | 1 | NA19055.hp1 | intron_variant | MODIFIER | c.371+893A>T | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 5/13 | chr14 | 51703481 | ||||||
chr14:51703603
|
C | G | 4 | a0001c0004t0005g0185a0001c0004t0005g0187a0001c0004t0005g0190others(1): Show | 4 | HG02083.hp2 NA18994.hp2 NA19055.hp1 others(1): Show |
intron_variant | MODIFIER | c.371+1015C>G | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 5/13 | chr14 | 51703603 | ||||||
chr14:51704024
|
A | C | 1 | a0001c0004t0016g0070 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.372-725A>C | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 5/13 | chr14 | 51704024 | ||||||
chr14:51704072
|
G | T | 3 | a0001c0001t0002g0010a0001c0001t0002g0155a0001c0001t0002g0156 | 5 | HG00673.hp1 NA18944.hp2 NA18966.hp1 others(2): Show |
intron_variant | MODIFIER | c.372-677G>T | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 5/13 | chr14 | 51704072 | ||||||
chr14:51704119
|
T | A | 1 | a0001c0003t0001g0269 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.372-630T>A | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 5/13 | chr14 | 51704119 | ||||||
chr14:51704367
|
C | T | 1 | a0001c0011t0001g0256 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.372-382C>T | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 5/13 | chr14 | 51704367 | ||||||
chr14:51704371
|
T | C | 1 | a0001c0001t0002g0171 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.372-378T>C | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 5/13 | chr14 | 51704371 | ||||||
chr14:51704373
|
T | C | 97 | a0001c0002t0001g0166a0001c0003t0001g0006a0001c0003t0001g0011others(94): Show | 120 | HG00140.hp1 HG00323.hp1 HG00438.hp1 others(117): Show |
intron_variant | MODIFIER | c.372-376T>C | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 5/13 | chr14 | 51704373 | ||||||
chr14:51704570
|
A | G | 35 | a0001c0001t0001g0164a0001c0001t0001g0168a0001c0001t0002g0002others(32): Show | 49 | HG00544.hp1 HG00597.hp1 HG00609.hp2 others(46): Show |
intron_variant | MODIFIER | c.372-179A>G | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 5/13 | chr14 | 51704570 | ||||||
chr14:51704691
|
T | G | 4 | a0001c0004t0005g0185a0001c0004t0005g0187a0001c0004t0005g0190others(1): Show | 4 | HG02083.hp2 NA18994.hp2 NA19055.hp1 others(1): Show |
intron_variant | MODIFIER | c.372-58T>G | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 5/13 | chr14 | 51704691 | ||||||
chr14:51705008
|
C | T | 31 | a0001c0002t0001g0007a0001c0002t0001g0074a0001c0002t0001g0075others(28): Show | 40 | HG00597.hp2 HG00609.hp1 HG00673.hp2 others(37): Show |
intron_variant | MODIFIER | c.558+73C>T | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 6/13 | chr14 | 51705008 | ||||||
chr14:51705034
|
T | G | 2 | a0001c0002t0001g0150a0001c0002t0001g0215 | 2 | HG02559.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.558+99T>G | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 6/13 | chr14 | 51705034 | ||||||
chr14:51705188
|
C | T | 1 | a0001c0003t0001g0263 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.558+253C>T | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 6/13 | chr14 | 51705188 | ||||||
chr14:51705311
|
C | G | 1 | a0001c0002t0002g0224 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.558+376C>G | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 6/13 | chr14 | 51705311 | ||||||
chr14:51705371
|
C | G | 4 | a0001c0004t0001g0063a0001c0004t0001g0066a0001c0004t0001g0067others(1): Show | 4 | HG00280.hp1 HG01167.hp2 HG02698.hp2 others(1): Show |
intron_variant | MODIFIER | c.558+436C>G | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 6/13 | chr14 | 51705371 | ||||||
chr14:51705429
|
C | T | 2 | a0002c0008t0009g0072a0002c0008t0009g0291 | 2 | HG02258.hp2 HG02572.hp2 |
intron_variant | MODIFIER | c.558+494C>T | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 6/13 | chr14 | 51705429 | ||||||
chr14:51705430
|
G | A | 15 | a0001c0001t0001g0202a0001c0001t0001g0209a0001c0001t0002g0012others(12): Show | 19 | HG00099.hp2 HG01074.hp2 HG01099.hp2 others(16): Show |
intron_variant | MODIFIER | c.558+495G>A | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 6/13 | chr14 | 51705430 | ||||||
chr14:51705433
|
T | G | 1 | a0001c0003t0001g0279 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.558+498T>G | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 6/13 | chr14 | 51705433 | ||||||
chr14:51705618
|
A | G | 4 | a0001c0004t0001g0140a0001c0004t0001g0141a0001c0004t0001g0207others(1): Show | 4 | HG02723.hp2 HG03098.hp1 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.558+683A>G | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 6/13 | chr14 | 51705618 | ||||||
chr14:51705648
|
A | G | 1 | a0001c0001t0002g0146 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.558+713A>G | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 6/13 | chr14 | 51705648 | ||||||
chr14:51705793
|
A | G | 2 | a0002c0008t0009g0072a0002c0008t0009g0291 | 2 | HG02258.hp2 HG02572.hp2 |
intron_variant | MODIFIER | c.558+858A>G | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 6/13 | chr14 | 51705793 | ||||||
chr14:51705923
|
A | T | 1 | a0001c0002t0001g0174 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.558+988A>T | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 6/13 | chr14 | 51705923 | ||||||
chr14:51705981
|
G | T | 194 | a0001c0001t0001g0113a0001c0001t0001g0164a0001c0001t0001g0168others(191): Show | 241 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(238): Show |
intron_variant | MODIFIER | c.558+1046G>T | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 6/13 | chr14 | 51705981 | ||||||
chr14:51706025
|
G | A | 2 | a0002c0008t0009g0072a0002c0008t0009g0291 | 2 | HG02258.hp2 HG02572.hp2 |
intron_variant | MODIFIER | c.558+1090G>A | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 6/13 | chr14 | 51706025 | ||||||
chr14:51706163
|
T | C | 4 | a0001c0004t0005g0185a0001c0004t0005g0187a0001c0004t0005g0190others(1): Show | 4 | HG02083.hp2 NA18994.hp2 NA19055.hp1 others(1): Show |
intron_variant | MODIFIER | c.558+1228T>C | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 6/13 | chr14 | 51706163 | ||||||
chr14:51706521
|
T | G | 6 | a0001c0001t0002g0147a0001c0001t0002g0148a0001c0001t0007g0095others(3): Show | 6 | HG00733.hp2 HG01109.hp2 HG01261.hp2 others(3): Show |
intron_variant | MODIFIER | c.559-1557T>G | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 6/13 | chr14 | 51706521 | ||||||
chr14:51706780
|
A | T | 10 | a0001c0002t0001g0196a0001c0004t0001g0046a0001c0004t0001g0063others(7): Show | 10 | HG00280.hp1 HG00639.hp1 HG01109.hp1 others(7): Show |
intron_variant | MODIFIER | c.559-1298A>T | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 6/13 | chr14 | 51706780 | ||||||
chr14:51706985
|
T | C | 80 | a0001c0003t0001g0006a0001c0003t0001g0011a0001c0003t0001g0014others(77): Show | 101 | HG00140.hp1 HG00323.hp1 HG00438.hp1 others(98): Show |
intron_variant | MODIFIER | c.559-1093T>C | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 6/13 | chr14 | 51706985 | ||||||
chr14:51707027
|
C | CT | 14 | a0001c0001t0002g0047a0001c0001t0002g0048a0001c0001t0002g0049others(11): Show | 14 | HG00738.hp1 HG01168.hp2 HG01256.hp1 others(11): Show |
intron_variant | MODIFIER | c.559-1050dupT | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr14 | 51707027 | |||||
chr14:51707660
|
A | T | 213 | a0001c0001t0001g0113a0001c0001t0001g0164a0001c0001t0001g0168others(210): Show | 262 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(259): Show |
intron_variant | MODIFIER | c.559-418A>T | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 6/13 | chr14 | 51707660 | ||||||
chr14:51707761
|
G | T | 1 | a0001c0003t0001g0276 | 1 | NA19067.hp2 | intron_variant | MODIFIER | c.559-317G>T | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 6/13 | chr14 | 51707761 | ||||||
chr14:51707805
|
A | T | 2 | a0002c0008t0009g0072a0002c0008t0009g0291 | 2 | HG02258.hp2 HG02572.hp2 |
intron_variant | MODIFIER | c.559-273A>T | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 6/13 | chr14 | 51707805 | ||||||
chr14:51707872
|
C | T | 1 | a0001c0004t0016g0070 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.559-206C>T | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 6/13 | chr14 | 51707872 | ||||||
chr14:51707959
|
A | C | 10 | a0001c0004t0001g0035a0001c0006t0003g0027a0001c0006t0003g0073others(7): Show | 12 | HG01358.hp1 HG01433.hp1 HG02145.hp2 others(9): Show |
intron_variant | MODIFIER | c.559-119A>C | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 6/13 | chr14 | 51707959 | ||||||
chr14:51708243
|
G | A | 1 | a0001c0004t0016g0070 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.714+10G>A | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 7/13 | chr14 | 51708243 | ||||||
chr14:51708329
|
C | A | 198 | a0001c0001t0001g0113a0001c0001t0001g0164a0001c0001t0001g0168others(195): Show | 247 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(244): Show |
intron_variant | MODIFIER | c.714+96C>A | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 7/13 | chr14 | 51708329 | ||||||
chr14:51708613
|
A | C | 6 | a0001c0003t0001g0017a0001c0003t0001g0228a0001c0003t0001g0271others(3): Show | 8 | HG01070.hp2 HG01071.hp1 HG01123.hp1 others(5): Show |
intron_variant | MODIFIER | c.714+380A>C | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 7/13 | chr14 | 51708613 | ||||||
chr14:51708715
|
T | A | 9 | a0001c0002t0001g0196a0001c0004t0001g0046a0001c0004t0001g0063others(6): Show | 9 | HG00280.hp1 HG00639.hp1 HG01109.hp1 others(6): Show |
intron_variant | MODIFIER | c.714+482T>A | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 7/13 | chr14 | 51708715 | ||||||
chr14:51708763
|
T | A | 89 | a0001c0003t0001g0006a0001c0003t0001g0011a0001c0003t0001g0014others(86): Show | 111 | HG00140.hp1 HG00323.hp1 HG00438.hp1 others(108): Show |
intron_variant | MODIFIER | c.714+530T>A | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 7/13 | chr14 | 51708763 | ||||||
chr14:51708956
|
C | T | 4 | a0001c0004t0001g0140a0001c0004t0001g0141a0001c0004t0001g0207others(1): Show | 4 | HG02723.hp2 HG03098.hp1 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.714+723C>T | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 7/13 | chr14 | 51708956 | ||||||
chr14:51709134
|
G | A | 79 | a0001c0003t0001g0006a0001c0003t0001g0011a0001c0003t0001g0014others(76): Show | 99 | HG00140.hp1 HG00323.hp1 HG00438.hp1 others(96): Show |
intron_variant | MODIFIER | c.714+901G>A | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 7/13 | chr14 | 51709134 | ||||||
chr14:51709359
|
G | A | 1 | a0001c0004t0001g0141 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.714+1126G>A | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 7/13 | chr14 | 51709359 | ||||||
chr14:51709363
|
C | A | 1 | a0001c0003t0001g0045 | 2 | HG03239.hp2 HG03710.hp1 |
intron_variant | MODIFIER | c.714+1130C>A | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 7/13 | chr14 | 51709363 | ||||||
chr14:51709564
|
A | G | 4 | a0001c0003t0001g0098a0001c0003t0001g0099a0001c0007t0001g0053others(1): Show | 4 | HG02630.hp1 HG03453.hp1 HG03540.hp2 others(1): Show |
intron_variant | MODIFIER | c.714+1331A>G | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 7/13 | chr14 | 51709564 | ||||||
chr14:51709655
|
C | G | 4 | a0001c0004t0005g0185a0001c0004t0005g0187a0001c0004t0005g0190others(1): Show | 4 | HG02083.hp2 NA18994.hp2 NA19055.hp1 others(1): Show |
intron_variant | MODIFIER | c.714+1422C>G | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 7/13 | chr14 | 51709655 | ||||||
chr14:51709715
|
A | G | 1 | a0001c0003t0001g0275 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.714+1482A>G | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 7/13 | chr14 | 51709715 | ||||||
chr14:51709859
|
C | T | 1 | a0001c0001t0002g0171 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.714+1626C>T | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 7/13 | chr14 | 51709859 | ||||||
chr14:51709893
|
G | T | 11 | a0001c0004t0001g0046a0001c0004t0001g0063a0001c0004t0001g0064others(8): Show | 11 | HG00280.hp1 HG00639.hp1 HG01109.hp1 others(8): Show |
intron_variant | MODIFIER | c.715-1638G>T | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 7/13 | chr14 | 51709893 | ||||||
chr14:51709894
|
A | T | 11 | a0001c0004t0001g0046a0001c0004t0001g0063a0001c0004t0001g0064others(8): Show | 11 | HG00280.hp1 HG00639.hp1 HG01109.hp1 others(8): Show |
intron_variant | MODIFIER | c.715-1637A>T | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 7/13 | chr14 | 51709894 | ||||||
chr14:51709913
|
A | T | 4 | a0001c0004t0005g0185a0001c0004t0005g0187a0001c0004t0005g0190others(1): Show | 4 | HG02083.hp2 NA18994.hp2 NA19055.hp1 others(1): Show |
intron_variant | MODIFIER | c.715-1618A>T | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 7/13 | chr14 | 51709913 | ||||||
chr14:51709950
|
T | C | 1 | a0003c0010t0001g0071 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.715-1581T>C | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 7/13 | chr14 | 51709950 | ||||||
chr14:51710045
|
G | A | 9 | a0001c0001t0002g0047a0001c0001t0002g0143a0001c0001t0002g0144others(6): Show | 9 | HG01891.hp2 HG02109.hp1 HG02280.hp1 others(6): Show |
intron_variant | MODIFIER | c.715-1486G>A | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 7/13 | chr14 | 51710045 | ||||||
chr14:51710156
|
G | A | 9 | a0001c0004t0001g0046a0001c0004t0001g0063a0001c0004t0001g0064others(6): Show | 9 | HG00280.hp1 HG00639.hp1 HG01109.hp1 others(6): Show |
intron_variant | MODIFIER | c.715-1375G>A | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 7/13 | chr14 | 51710156 | ||||||
chr14:51710222
|
T | C | 8 | a0001c0002t0001g0031a0001c0002t0001g0032a0001c0002t0001g0033others(5): Show | 11 | HG00099.hp1 HG00741.hp2 HG01070.hp1 others(8): Show |
intron_variant | MODIFIER | c.715-1309T>C | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 7/13 | chr14 | 51710222 | ||||||
chr14:51710270
|
A | C | 103 | a0001c0001t0001g0113a0001c0001t0001g0164a0001c0001t0001g0168others(100): Show | 129 | HG00099.hp2 HG00140.hp2 HG00544.hp1 others(126): Show |
intron_variant | MODIFIER | c.715-1261A>C | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 7/13 | chr14 | 51710270 | ||||||
chr14:51710310
|
G | A | 9 | a0001c0001t0002g0047a0001c0001t0002g0143a0001c0001t0002g0144others(6): Show | 9 | HG01891.hp2 HG02109.hp1 HG02280.hp1 others(6): Show |
intron_variant | MODIFIER | c.715-1221G>A | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 7/13 | chr14 | 51710310 | ||||||
chr14:51710402
|
C | T | 1 | a0001c0004t0012g0182 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.715-1129C>T | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 7/13 | chr14 | 51710402 | ||||||
chr14:51710455
|
T | C | 1 | a0001c0001t0002g0048 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.715-1076T>C | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 7/13 | chr14 | 51710455 | ||||||
chr14:51710697
|
C | G | 1 | a0001c0001t0002g0110 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.715-834C>G | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 7/13 | chr14 | 51710697 | ||||||
chr14:51710809
|
G | A | 1 | a0001c0004t0012g0182 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.715-722G>A | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 7/13 | chr14 | 51710809 | ||||||
chr14:51710871
|
A | G | 104 | a0001c0001t0001g0113a0001c0001t0001g0164a0001c0001t0001g0168others(101): Show | 130 | HG00099.hp2 HG00140.hp2 HG00544.hp1 others(127): Show |
intron_variant | MODIFIER | c.715-660A>G | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 7/13 | chr14 | 51710871 | ||||||
chr14:51711177
|
AAATC | A | 102 | a0001c0001t0001g0113a0001c0001t0001g0164a0001c0001t0001g0168others(99): Show | 128 | HG00099.hp2 HG00140.hp2 HG00544.hp1 others(125): Show |
intron_variant | MODIFIER | c.715-351_715-348del others(4): Show |
FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 7/13 | INFO_REALIGN_3_PRIME | chr14 | 51711177 | |||||
chr14:51711253
|
A | C | 2 | a0002c0008t0009g0072a0002c0008t0009g0291 | 2 | HG02258.hp2 HG02572.hp2 |
intron_variant | MODIFIER | c.715-278A>C | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 7/13 | chr14 | 51711253 | ||||||
chr14:51711320
|
G | C | 104 | a0001c0001t0001g0113a0001c0001t0001g0164a0001c0001t0001g0168others(101): Show | 130 | HG00099.hp2 HG00140.hp2 HG00544.hp1 others(127): Show |
intron_variant | MODIFIER | c.715-211G>C | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 7/13 | chr14 | 51711320 | ||||||
chr14:51711360
|
T | G | 10 | a0001c0001t0001g0113a0001c0001t0002g0054a0001c0001t0002g0114others(7): Show | 10 | HG01891.hp1 HG02486.hp1 HG02717.hp1 others(7): Show |
intron_variant | MODIFIER | c.715-171T>G | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 7/13 | chr14 | 51711360 | ||||||
chr14:51711444
|
C | T | 1 | a0001c0002t0001g0200 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.715-87C>T | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 7/13 | chr14 | 51711444 | ||||||
chr14:51711902
|
G | A | 4 | a0001c0004t0005g0185a0001c0004t0005g0187a0001c0004t0005g0190others(1): Show | 4 | HG02083.hp2 NA18994.hp2 NA19055.hp1 others(1): Show |
intron_variant | MODIFIER | c.780+306G>A | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 8/13 | chr14 | 51711902 | ||||||
chr14:51712173
|
A | C | 105 | a0001c0001t0001g0113a0001c0001t0001g0164a0001c0001t0001g0168others(102): Show | 131 | HG00099.hp2 HG00140.hp2 HG00323.hp2 others(128): Show |
intron_variant | MODIFIER | c.781-310A>C | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 8/13 | chr14 | 51712173 | ||||||
chr14:51712268
|
C | T | 1 | a0001c0004t0016g0070 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.781-215C>T | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 8/13 | chr14 | 51712268 | ||||||
chr14:51712341
|
T | C | 105 | a0001c0001t0001g0113a0001c0001t0001g0164a0001c0001t0001g0168others(102): Show | 132 | HG00099.hp2 HG00140.hp2 HG00323.hp2 others(129): Show |
intron_variant | MODIFIER | c.781-142T>C | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 8/13 | chr14 | 51712341 | ||||||
chr14:51712733
|
T | G | 215 | a0001c0001t0001g0113a0001c0001t0001g0164a0001c0001t0001g0168others(212): Show | 264 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(261): Show |
intron_variant | MODIFIER | c.849+182T>G | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 9/13 | chr14 | 51712733 | ||||||
chr14:51712874
|
G | A | 2 | a0001c0003t0001g0011a0001c0003t0001g0034 | 5 | HG02818.hp1 HG02886.hp1 HG03041.hp1 others(2): Show |
intron_variant | MODIFIER | c.849+323G>A | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 9/13 | chr14 | 51712874 | ||||||
chr14:51713080
|
G | A | 102 | a0001c0001t0001g0113a0001c0001t0001g0164a0001c0001t0001g0168others(99): Show | 128 | HG00099.hp2 HG00140.hp2 HG00544.hp1 others(125): Show |
intron_variant | MODIFIER | c.849+529G>A | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 9/13 | chr14 | 51713080 | ||||||
chr14:51713083
|
T | C | 80 | a0001c0003t0001g0006a0001c0003t0001g0011a0001c0003t0001g0014others(77): Show | 101 | HG00140.hp1 HG00323.hp1 HG00438.hp1 others(98): Show |
intron_variant | MODIFIER | c.849+532T>C | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 9/13 | chr14 | 51713083 | ||||||
chr14:51713106
|
G | GT | 5 | a0001c0001t0002g0020a0001c0001t0002g0061a0001c0001t0002g0062others(2): Show | 6 | HG00099.hp2 HG01516.hp1 HG01943.hp1 others(3): Show |
intron_variant | MODIFIER | c.849+561dupT | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 9/13 | INFO_REALIGN_3_PRIME | chr14 | 51713106 | |||||
chr14:51713178
|
C | T | 1 | a0001c0002t0001g0289 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.849+627C>T | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 9/13 | chr14 | 51713178 | ||||||
chr14:51713235
|
A | G | 1 | a0001c0001t0002g0231 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.849+684A>G | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 9/13 | chr14 | 51713235 | ||||||
chr14:51713382
|
C | T | 1 | a0001c0003t0001g0257 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.849+831C>T | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 9/13 | chr14 | 51713382 | ||||||
chr14:51713458
|
CA | C | 193 | a0001c0001t0001g0113a0001c0001t0001g0168a0001c0001t0001g0202others(190): Show | 241 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(238): Show |
intron_variant | MODIFIER | c.849+926delA | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 9/13 | INFO_REALIGN_3_PRIME | chr14 | 51713458 | |||||
chr14:51713480
|
G | A | 102 | a0001c0001t0001g0113a0001c0001t0001g0164a0001c0001t0001g0168others(99): Show | 128 | HG00099.hp2 HG00140.hp2 HG00544.hp1 others(125): Show |
intron_variant | MODIFIER | c.849+929G>A | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 9/13 | chr14 | 51713480 | ||||||
chr14:51713520
|
GA | G | 5 | a0001c0001t0002g0020a0001c0001t0002g0061a0001c0001t0002g0062others(2): Show | 6 | HG00099.hp2 HG01516.hp1 HG01943.hp1 others(3): Show |
intron_variant | MODIFIER | c.849+970delA | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 9/13 | chr14 | 51713520 | ||||||
chr14:51713602
|
C | T | 2 | a0001c0001t0002g0054a0001c0001t0002g0114 | 2 | HG01891.hp1 HG02895.hp1 |
intron_variant | MODIFIER | c.849+1051C>T | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 9/13 | chr14 | 51713602 | ||||||
chr14:51713729
|
A | G | 6 | a0001c0001t0002g0147a0001c0001t0002g0148a0001c0001t0002g0160others(3): Show | 6 | HG02886.hp2 HG02922.hp1 NA18522.hp2 others(3): Show |
intron_variant | MODIFIER | c.849+1178A>G | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 9/13 | chr14 | 51713729 | ||||||
chr14:51713757
|
A | G | 1 | a0001c0001t0002g0109 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.849+1206A>G | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 9/13 | chr14 | 51713757 | ||||||
chr14:51713990
|
C | A | 2 | a0002c0008t0009g0072a0002c0008t0009g0291 | 2 | HG02258.hp2 HG02572.hp2 |
intron_variant | MODIFIER | c.850-1335C>A | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 9/13 | chr14 | 51713990 | ||||||
chr14:51714008
|
G | C | 102 | a0001c0001t0001g0113a0001c0001t0001g0164a0001c0001t0001g0168others(99): Show | 128 | HG00099.hp2 HG00140.hp2 HG00544.hp1 others(125): Show |
intron_variant | MODIFIER | c.850-1317G>C | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 9/13 | chr14 | 51714008 | ||||||
chr14:51714268
|
A | T | 101 | a0001c0001t0001g0113a0001c0001t0001g0164a0001c0001t0001g0168others(98): Show | 127 | HG00099.hp2 HG00140.hp2 HG00544.hp1 others(124): Show |
intron_variant | MODIFIER | c.850-1057A>T | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 9/13 | chr14 | 51714268 | ||||||
chr14:51714316
|
T | G | 1 | a0001c0001t0002g0117 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.850-1009T>G | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 9/13 | chr14 | 51714316 | ||||||
chr14:51714317
|
TA | T | 101 | a0001c0001t0001g0113a0001c0001t0001g0164a0001c0001t0001g0168others(98): Show | 127 | HG00099.hp2 HG00140.hp2 HG00544.hp1 others(124): Show |
intron_variant | MODIFIER | c.850-998delA | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 9/13 | INFO_REALIGN_3_PRIME | chr14 | 51714317 | |||||
chr14:51714327
|
A | G | 101 | a0001c0001t0001g0113a0001c0001t0001g0164a0001c0001t0001g0168others(98): Show | 127 | HG00099.hp2 HG00140.hp2 HG00544.hp1 others(124): Show |
intron_variant | MODIFIER | c.850-998A>G | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 9/13 | chr14 | 51714327 | ||||||
chr14:51714347
|
C | T | 316 | a0001c0001t0001g0113a0001c0001t0001g0164a0001c0001t0001g0168others(313): Show | 389 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(386): Show |
intron_variant | MODIFIER | c.850-978C>T | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 9/13 | chr14 | 51714347 | ||||||
chr14:51714381
|
A | G | 11 | a0001c0004t0001g0035a0001c0004t0016g0070a0001c0006t0003g0027others(8): Show | 13 | HG01358.hp1 HG01433.hp1 HG02145.hp2 others(10): Show |
intron_variant | MODIFIER | c.850-944A>G | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 9/13 | chr14 | 51714381 | ||||||
chr14:51714650
|
A | C | 102 | a0001c0001t0001g0113a0001c0001t0001g0164a0001c0001t0001g0168others(99): Show | 128 | HG00099.hp2 HG00140.hp2 HG00544.hp1 others(125): Show |
intron_variant | MODIFIER | c.850-675A>C | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 9/13 | chr14 | 51714650 | ||||||
chr14:51714750
|
T | C | 1 | a0001c0003t0001g0259 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.850-575T>C | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 9/13 | chr14 | 51714750 | ||||||
chr14:51714865
|
A | G | 1 | a0001c0004t0016g0070 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.850-460A>G | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 9/13 | chr14 | 51714865 | ||||||
chr14:51714909
|
G | A | 102 | a0001c0001t0001g0113a0001c0001t0001g0164a0001c0001t0001g0168others(99): Show | 128 | HG00099.hp2 HG00140.hp2 HG00544.hp1 others(125): Show |
intron_variant | MODIFIER | c.850-416G>A | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 9/13 | chr14 | 51714909 | ||||||
chr14:51715046
|
C | T | 77 | a0001c0003t0001g0006a0001c0003t0001g0011a0001c0003t0001g0014others(74): Show | 98 | HG00140.hp1 HG00323.hp1 HG00438.hp1 others(95): Show |
intron_variant | MODIFIER | c.850-279C>T | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 9/13 | chr14 | 51715046 | ||||||
chr14:51715080
|
G | C | 2 | a0001c0001t0002g0203a0001c0001t0002g0211 | 2 | HG01074.hp2 HG01099.hp2 |
intron_variant | MODIFIER | c.850-245G>C | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 9/13 | chr14 | 51715080 | ||||||
chr14:51715192
|
C | T | 4 | a0001c0004t0005g0185a0001c0004t0005g0187a0001c0004t0005g0190others(1): Show | 4 | HG02083.hp2 NA18994.hp2 NA19055.hp1 others(1): Show |
intron_variant | MODIFIER | c.850-133C>T | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 9/13 | chr14 | 51715192 | ||||||
chr14:51715219
|
A | G | 4 | a0001c0004t0005g0185a0001c0004t0005g0187a0001c0004t0005g0190others(1): Show | 4 | HG02083.hp2 NA18994.hp2 NA19055.hp1 others(1): Show |
intron_variant | MODIFIER | c.850-106A>G | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 9/13 | chr14 | 51715219 | ||||||
chr14:51715607
|
A | G | 1 | a0001c0002t0001g0087 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.1024+108A>G | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 10/13 | chr14 | 51715607 | ||||||
chr14:51715688
|
T | C | 208 | a0001c0001t0001g0113a0001c0001t0001g0164a0001c0001t0001g0168others(205): Show | 257 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(254): Show |
intron_variant | MODIFIER | c.1024+189T>C | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 10/13 | chr14 | 51715688 | ||||||
chr14:51715761
|
A | T | 1 | a0001c0001t0002g0311 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.1024+262A>T | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 10/13 | chr14 | 51715761 | ||||||
chr14:51715783
|
C | CA | 4 | a0001c0004t0005g0185a0001c0004t0005g0187a0001c0004t0005g0190others(1): Show | 4 | HG02083.hp2 NA18994.hp2 NA19055.hp1 others(1): Show |
intron_variant | MODIFIER | c.1024+289dupA | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 10/13 | INFO_REALIGN_3_PRIME | chr14 | 51715783 | |||||
chr14:51715850
|
A | T | 73 | a0001c0003t0001g0006a0001c0003t0001g0011a0001c0003t0001g0014others(70): Show | 94 | HG00140.hp1 HG00323.hp1 HG00438.hp1 others(91): Show |
intron_variant | MODIFIER | c.1024+351A>T | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 10/13 | chr14 | 51715850 | ||||||
chr14:51716124
|
C | T | 1 | a0001c0003t0001g0271 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.1024+625C>T | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 10/13 | chr14 | 51716124 | ||||||
chr14:51716296
|
G | T | 1 | a0001c0002t0002g0224 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.1024+797G>T | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 10/13 | chr14 | 51716296 | ||||||
chr14:51716599
|
A | G | 1 | a0001c0001t0002g0149 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.1024+1100A>G | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 10/13 | chr14 | 51716599 | ||||||
chr14:51716687
|
T | G | 1 | a0001c0001t0002g0230 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.1024+1188T>G | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 10/13 | chr14 | 51716687 | ||||||
chr14:51716887
|
C | G | 206 | a0001c0001t0001g0113a0001c0001t0001g0164a0001c0001t0001g0168others(203): Show | 255 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(252): Show |
intron_variant | MODIFIER | c.1024+1388C>G | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 10/13 | chr14 | 51716887 | ||||||
chr14:51716929
|
C | T | 1 | a0001c0001t0002g0144 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.1024+1430C>T | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 10/13 | chr14 | 51716929 | ||||||
chr14:51717025
|
C | G | 1 | a0001c0002t0001g0196 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.1024+1526C>G | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 10/13 | chr14 | 51717025 | ||||||
chr14:51717168
|
G | A | 2 | a0001c0001t0011g0131a0001c0001t0011g0132 | 2 | HG02896.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.1024+1669G>A | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 10/13 | chr14 | 51717168 | ||||||
chr14:51717172
|
CTTTG | C | 4 | a0001c0004t0001g0140a0001c0004t0001g0141a0001c0004t0001g0207others(1): Show | 4 | HG02723.hp2 HG03098.hp1 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.1024+1681_1024+168 others(8): Show |
FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 10/13 | INFO_REALIGN_3_PRIME | chr14 | 51717172 | |||||
chr14:51717187
|
G | A | 1 | a0001c0001t0002g0120 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.1024+1688G>A | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 10/13 | chr14 | 51717187 | ||||||
chr14:51717271
|
G | A | 1 | a0001c0003t0001g0293 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.1024+1772G>A | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 10/13 | chr14 | 51717271 | ||||||
chr14:51717359
|
G | A | 2 | a0001c0001t0002g0012a0004c0012t0002g0210 | 4 | HG02809.hp1 HG03041.hp2 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.1024+1860G>A | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 10/13 | chr14 | 51717359 | ||||||
chr14:51717379
|
G | A | 71 | a0001c0001t0001g0113a0001c0001t0001g0164a0001c0001t0001g0168others(68): Show | 93 | HG00140.hp2 HG00544.hp1 HG00597.hp1 others(90): Show |
intron_variant | MODIFIER | c.1024+1880G>A | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 10/13 | chr14 | 51717379 | ||||||
chr14:51717440
|
C | G | 1 | a0001c0003t0001g0282 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.1024+1941C>G | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 10/13 | chr14 | 51717440 | ||||||
chr14:51717516
|
A | G | 1 | a0001c0004t0012g0182 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.1024+2017A>G | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 10/13 | chr14 | 51717516 | ||||||
chr14:51717655
|
G | A | 1 | a0001c0003t0001g0274 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.1024+2156G>A | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 10/13 | chr14 | 51717655 | ||||||
chr14:51717710
|
A | G | 1 | a0001c0001t0002g0081 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.1024+2211A>G | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 10/13 | chr14 | 51717710 | ||||||
chr14:51717721
|
C | G | 103 | a0001c0001t0001g0113a0001c0001t0001g0164a0001c0001t0001g0168others(100): Show | 129 | HG00099.hp2 HG00140.hp2 HG00544.hp1 others(126): Show |
intron_variant | MODIFIER | c.1024+2222C>G | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 10/13 | chr14 | 51717721 | ||||||
chr14:51717882
|
C | A | 9 | a0001c0004t0001g0046a0001c0004t0001g0063a0001c0004t0001g0064others(6): Show | 9 | HG00280.hp1 HG00639.hp1 HG01109.hp1 others(6): Show |
intron_variant | MODIFIER | c.1025-2173C>A | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 10/13 | chr14 | 51717882 | ||||||
chr14:51717888
|
G | A | 1 | a0001c0001t0002g0231 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.1025-2167G>A | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 10/13 | chr14 | 51717888 | ||||||
chr14:51718106
|
C | T | 1 | a0001c0003t0001g0055 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.1025-1949C>T | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 10/13 | chr14 | 51718106 | ||||||
chr14:51718139
|
G | A | 4 | a0001c0003t0001g0015a0001c0003t0001g0254a0001c0003t0001g0263others(1): Show | 6 | HG01081.hp2 HG01106.hp2 HG01167.hp1 others(3): Show |
intron_variant | MODIFIER | c.1025-1916G>A | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 10/13 | chr14 | 51718139 | ||||||
chr14:51718266
|
G | A | 101 | a0001c0001t0001g0113a0001c0001t0001g0164a0001c0001t0001g0168others(98): Show | 127 | HG00099.hp2 HG00140.hp2 HG00544.hp1 others(124): Show |
intron_variant | MODIFIER | c.1025-1789G>A | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 10/13 | chr14 | 51718266 | ||||||
chr14:51718352
|
A | G | 1 | a0001c0002t0001g0227 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.1025-1703A>G | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 10/13 | chr14 | 51718352 | ||||||
chr14:51718421
|
G | A | 212 | a0001c0001t0001g0113a0001c0001t0001g0164a0001c0001t0001g0168others(209): Show | 261 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(258): Show |
intron_variant | MODIFIER | c.1025-1634G>A | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 10/13 | chr14 | 51718421 | ||||||
chr14:51718487
|
T | G | 2 | a0001c0007t0001g0053a0001c0007t0001g0101 | 2 | HG02630.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.1025-1568T>G | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 10/13 | chr14 | 51718487 | ||||||
chr14:51718825
|
A | G | 1 | a0001c0013t0001g0201 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.1025-1230A>G | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 10/13 | chr14 | 51718825 | ||||||
chr14:51719068
|
T | A | 1 | a0001c0004t0016g0070 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.1025-987T>A | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 10/13 | chr14 | 51719068 | ||||||
chr14:51719117
|
C | T | 3 | a0001c0002t0001g0198a0001c0002t0001g0199a0001c0002t0001g0200 | 3 | HG02809.hp2 HG03579.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.1025-938C>T | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 10/13 | chr14 | 51719117 | ||||||
chr14:51719170
|
G | A | 9 | a0001c0004t0001g0046a0001c0004t0001g0063a0001c0004t0001g0064others(6): Show | 9 | HG00280.hp1 HG00639.hp1 HG01109.hp1 others(6): Show |
intron_variant | MODIFIER | c.1025-885G>A | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 10/13 | chr14 | 51719170 | ||||||
chr14:51719228
|
A | AG | 103 | a0001c0001t0001g0113a0001c0001t0001g0164a0001c0001t0001g0168others(100): Show | 129 | HG00099.hp2 HG00140.hp2 HG00323.hp2 others(126): Show |
intron_variant | MODIFIER | c.1025-827_1025-826i others(3): Show |
FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 10/13 | chr14 | 51719228 | ||||||
chr14:51719554
|
A | G | 2 | a0001c0003t0001g0221a0001c0003t0001g0229 | 2 | HG01192.hp1 HG01361.hp2 |
intron_variant | MODIFIER | c.1025-501A>G | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 10/13 | chr14 | 51719554 | ||||||
chr14:51719619
|
G | T | 1 | a0001c0003t0001g0254 | 1 | HG01257.hp2 | intron_variant | MODIFIER | c.1025-436G>T | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 10/13 | chr14 | 51719619 | ||||||
chr14:51719682
|
G | A | 1 | a0001c0001t0002g0160 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.1025-373G>A | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 10/13 | chr14 | 51719682 | ||||||
chr14:51719697
|
A | G | 1 | a0001c0004t0012g0182 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.1025-358A>G | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 10/13 | chr14 | 51719697 | ||||||
chr14:51719756
|
A | G | 3 | a0001c0002t0001g0042a0001c0002t0001g0057a0001c0004t0012g0182 | 4 | HG01496.hp2 HG03209.hp1 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.1025-299A>G | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 10/13 | chr14 | 51719756 | ||||||
chr14:51719848
|
T | C | 1 | a0001c0003t0001g0262 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.1025-207T>C | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 10/13 | chr14 | 51719848 | ||||||
chr14:51720011
|
G | A | 3 | a0001c0001t0011g0131a0001c0001t0011g0132a0001c0001t0024g0124 | 3 | HG02896.hp2 HG02897.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.1025-44G>A | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 10/13 | chr14 | 51720011 | ||||||
chr14:51720050
|
C | T | 1 | a0001c0003t0001g0267 | 1 | NA19079.hp2 | splice_region_variant&intron_variant | LOW | c.1025-5C>T | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 10/13 | chr14 | 51720050 | ||||||
chr14:51720555
|
G | A | 1 | a0001c0004t0016g0070 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.1360+165G>A | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 11/13 | chr14 | 51720555 | ||||||
chr14:51720775
|
C | T | 1 | a0001c0003t0001g0272 | 1 | NA19006.hp1 | intron_variant | MODIFIER | c.1360+385C>T | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 11/13 | chr14 | 51720775 | ||||||
chr14:51720851
|
A | T | 1 | a0001c0001t0002g0108 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.1360+461A>T | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 11/13 | chr14 | 51720851 | ||||||
chr14:51720914
|
A | G | 1 | a0001c0003t0001g0282 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.1360+524A>G | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 11/13 | chr14 | 51720914 | ||||||
chr14:51720917
|
A | G | 1 | a0001c0002t0001g0086 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.1360+527A>G | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 11/13 | chr14 | 51720917 | ||||||
chr14:51720932
|
C | T | 102 | a0001c0001t0001g0113a0001c0001t0001g0164a0001c0001t0001g0168others(99): Show | 128 | HG00099.hp2 HG00140.hp2 HG00323.hp2 others(125): Show |
intron_variant | MODIFIER | c.1360+542C>T | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 11/13 | chr14 | 51720932 | ||||||
chr14:51721178
|
T | C | 316 | a0001c0001t0001g0113a0001c0001t0001g0164a0001c0001t0001g0168others(313): Show | 389 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(386): Show |
intron_variant | MODIFIER | c.1361-771T>C | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 11/13 | chr14 | 51721178 | ||||||
chr14:51721267
|
G | T | 102 | a0001c0001t0001g0113a0001c0001t0001g0164a0001c0001t0001g0168others(99): Show | 128 | HG00099.hp2 HG00140.hp2 HG00544.hp1 others(125): Show |
intron_variant | MODIFIER | c.1361-682G>T | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 11/13 | chr14 | 51721267 | ||||||
chr14:51721285
|
A | ATAATCTT others(10): Show |
1 | a0001c0001t0002g0315 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.1361-664_1361-663i others(19): Show |
FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 11/13 | chr14 | 51721285 | ||||||
chr14:51721288
|
C | A | 1 | a0001c0001t0002g0315 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.1361-661C>A | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 11/13 | chr14 | 51721288 | ||||||
chr14:51721311
|
C | T | 2 | a0001c0001t0002g0012a0004c0012t0002g0210 | 4 | HG02809.hp1 HG03041.hp2 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.1361-638C>T | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 11/13 | chr14 | 51721311 | ||||||
chr14:51721388
|
G | A | 9 | a0001c0006t0003g0027a0001c0006t0003g0073a0001c0006t0003g0151others(6): Show | 10 | HG01358.hp1 HG01433.hp1 HG02145.hp2 others(7): Show |
intron_variant | MODIFIER | c.1361-561G>A | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 11/13 | chr14 | 51721388 | ||||||
chr14:51721409
|
A | G | 1 | a0001c0004t0016g0070 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.1361-540A>G | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 11/13 | chr14 | 51721409 | ||||||
chr14:51721426
|
A | G | 106 | a0001c0001t0001g0113a0001c0001t0001g0164a0001c0001t0001g0168others(103): Show | 132 | HG00099.hp2 HG00140.hp2 HG00323.hp2 others(129): Show |
intron_variant | MODIFIER | c.1361-523A>G | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 11/13 | chr14 | 51721426 | ||||||
chr14:51721481
|
G | C | 4 | a0001c0001t0001g0113a0001c0001t0002g0054a0001c0001t0002g0114others(1): Show | 4 | HG01891.hp1 HG02486.hp1 HG02895.hp1 others(1): Show |
intron_variant | MODIFIER | c.1361-468G>C | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 11/13 | chr14 | 51721481 | ||||||
chr14:51721488
|
C | T | 103 | a0001c0001t0001g0113a0001c0001t0001g0164a0001c0001t0001g0168others(100): Show | 129 | HG00099.hp2 HG00140.hp2 HG00323.hp2 others(126): Show |
intron_variant | MODIFIER | c.1361-461C>T | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 11/13 | chr14 | 51721488 | ||||||
chr14:51721645
|
GGGAA | G | 215 | a0001c0001t0001g0113a0001c0001t0001g0164a0001c0001t0001g0168others(212): Show | 265 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(262): Show |
intron_variant | MODIFIER | c.1361-287_1361-284d others(6): Show |
FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 11/13 | INFO_REALIGN_3_PRIME | chr14 | 51721645 | |||||
chr14:51721692
|
CAGGAAGG others(1): Show |
C | 80 | a0001c0003t0001g0006a0001c0003t0001g0011a0001c0003t0001g0014others(77): Show | 102 | HG00140.hp1 HG00323.hp1 HG00438.hp1 others(99): Show |
intron_variant | MODIFIER | c.1361-237_1361-230d others(10): Show |
FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 11/13 | INFO_REALIGN_3_PRIME | chr14 | 51721692 | |||||
chr14:51721696
|
A | AAGGAAGG others(69): Show |
7 | a0001c0006t0003g0027a0001c0006t0003g0073a0001c0006t0003g0151others(4): Show | 8 | HG01358.hp1 HG02145.hp2 HG02280.hp2 others(5): Show |
intron_variant | MODIFIER | c.1361-234_1361-233i others(78): Show |
FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 11/13 | INFO_REALIGN_3_PRIME | chr14 | 51721696 | |||||
chr14:51721696
|
A | AAGGAAGG others(69): Show |
1 | a0001c0006t0003g0153 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.1361-234_1361-233i others(78): Show |
FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 11/13 | INFO_REALIGN_3_PRIME | chr14 | 51721696 | |||||
chr14:51721700
|
A | AAGGAAGG others(69): Show |
1 | a0001c0004t0016g0070 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.1361-234_1361-233i others(78): Show |
FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 11/13 | INFO_REALIGN_3_PRIME | chr14 | 51721700 | |||||
chr14:51721708
|
A | AAGGG | 16 | a0001c0002t0001g0196a0001c0003t0001g0194a0001c0004t0001g0046others(13): Show | 16 | HG00280.hp1 HG00639.hp1 HG01109.hp1 others(13): Show |
intron_variant | MODIFIER | c.1361-238_1361-237i others(6): Show |
FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 11/13 | INFO_REALIGN_3_PRIME | chr14 | 51721708 | |||||
chr14:51721709
|
A | AGGAAGGG others(57): Show |
1 | a0001c0006t0022g0163 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.1361-234_1361-233i others(66): Show |
FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 11/13 | INFO_REALIGN_3_PRIME | chr14 | 51721709 | |||||
chr14:51721712
|
A | G | 106 | a0001c0001t0001g0113a0001c0001t0001g0164a0001c0001t0001g0168others(103): Show | 132 | HG00099.hp2 HG00140.hp2 HG00323.hp2 others(129): Show |
intron_variant | MODIFIER | c.1361-237A>G | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 11/13 | chr14 | 51721712 | ||||||
chr14:51721720
|
G | A | 103 | a0001c0001t0001g0113a0001c0001t0001g0164a0001c0001t0001g0168others(100): Show | 129 | HG00099.hp2 HG00140.hp2 HG00323.hp2 others(126): Show |
intron_variant | MODIFIER | c.1361-229G>A | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 11/13 | chr14 | 51721720 | ||||||
chr14:51721732
|
G | A | 121 | a0001c0001t0001g0113a0001c0001t0001g0164a0001c0001t0001g0168others(118): Show | 147 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(144): Show |
intron_variant | MODIFIER | c.1361-217G>A | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 11/13 | chr14 | 51721732 | ||||||
chr14:51721744
|
A | G | 1 | a0001c0004t0005g0187 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.1361-205A>G | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 11/13 | chr14 | 51721744 | ||||||
chr14:51721745
|
A | AGGAGGGA others(61): Show |
2 | a0001c0004t0001g0065a0001c0004t0001g0069 | 2 | HG01243.hp2 HG03834.hp1 |
intron_variant | MODIFIER | c.1361-202_1361-201i others(70): Show |
FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 11/13 | INFO_REALIGN_3_PRIME | chr14 | 51721745 | |||||
chr14:51721745
|
A | AGGAGGGA others(69): Show |
7 | a0001c0002t0001g0196a0001c0004t0001g0046a0001c0004t0001g0063others(4): Show | 7 | HG00280.hp1 HG00639.hp1 HG01109.hp1 others(4): Show |
intron_variant | MODIFIER | c.1361-202_1361-201i others(78): Show |
FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 11/13 | INFO_REALIGN_3_PRIME | chr14 | 51721745 | |||||
chr14:51721745
|
A | AGGAGGGA others(33): Show |
2 | a0002c0008t0009g0072a0002c0008t0009g0291 | 2 | HG02258.hp2 HG02572.hp2 |
intron_variant | MODIFIER | c.1361-202_1361-201i others(42): Show |
FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 11/13 | INFO_REALIGN_3_PRIME | chr14 | 51721745 | |||||
chr14:51721745
|
A | AGGAGGGA others(41): Show |
4 | a0001c0004t0001g0140a0001c0004t0001g0141a0001c0004t0001g0207others(1): Show | 4 | HG02723.hp1 HG02723.hp2 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.1361-202_1361-201i others(50): Show |
FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 11/13 | INFO_REALIGN_3_PRIME | chr14 | 51721745 | |||||
chr14:51721745
|
A | AGGAGGGA others(49): Show |
1 | a0001c0004t0001g0208 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.1361-202_1361-201i others(58): Show |
FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 11/13 | INFO_REALIGN_3_PRIME | chr14 | 51721745 | |||||
chr14:51721748
|
G | A | 20 | a0001c0002t0001g0127a0001c0002t0001g0196a0001c0003t0001g0194others(17): Show | 20 | HG00280.hp1 HG00639.hp1 HG01109.hp1 others(17): Show |
intron_variant | MODIFIER | c.1361-201G>A | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 11/13 | chr14 | 51721748 | ||||||
chr14:51721749
|
A | G | 2 | a0001c0003t0001g0194a0003c0010t0001g0071 | 2 | HG03139.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.1361-200A>G | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 11/13 | chr14 | 51721749 | ||||||
chr14:51721753
|
A | AGGAACAA others(177): Show |
1 | a0001c0002t0001g0127 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.1361-192_1361-191i others(186): Show |
FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 11/13 | INFO_REALIGN_3_PRIME | chr14 | 51721753 | |||||
chr14:51721753
|
A | AGGAAGGA others(1): Show |
98 | a0001c0002t0001g0004a0001c0002t0001g0007a0001c0002t0001g0013others(95): Show | 121 | HG00099.hp1 HG00280.hp2 HG00438.hp2 others(118): Show |
intron_variant | MODIFIER | c.1361-179_1361-172d others(10): Show |
FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 11/13 | INFO_REALIGN_3_PRIME | chr14 | 51721753 | |||||
chr14:51721753
|
A | AGGAAGGA others(105): Show |
1 | a0001c0002t0001g0265 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.1361-172_1361-171i others(114): Show |
FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 11/13 | INFO_REALIGN_3_PRIME | chr14 | 51721753 | |||||
chr14:51721753
|
A | AGGAAGGA others(22): Show |
10 | a0001c0004t0001g0035a0001c0004t0016g0070a0001c0006t0003g0027others(7): Show | 12 | HG01358.hp1 HG02145.hp2 HG02280.hp2 others(9): Show |
intron_variant | MODIFIER | c.1361-182_1361-181i others(31): Show |
FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 11/13 | INFO_REALIGN_3_PRIME | chr14 | 51721753 | |||||
chr14:51721753
|
A | AGGAAGGA others(30): Show |
1 | a0001c0006t0022g0163 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.1361-182_1361-181i others(39): Show |
FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 11/13 | INFO_REALIGN_3_PRIME | chr14 | 51721753 | |||||
chr14:51721753
|
A | AGGAAGGA others(139): Show |
3 | a0001c0004t0005g0185a0001c0004t0005g0190a0001c0004t0005g0292 | 3 | NA18994.hp2 NA19055.hp1 NA19082.hp2 |
intron_variant | MODIFIER | c.1361-182_1361-181i others(148): Show |
FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 11/13 | INFO_REALIGN_3_PRIME | chr14 | 51721753 | |||||
chr14:51721753
|
A | AGGAAGGG others(151): Show |
1 | a0001c0004t0005g0187 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.1361-190_1361-189i others(160): Show |
FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 11/13 | INFO_REALIGN_3_PRIME | chr14 | 51721753 | |||||
chr14:51721753
|
A | AGGAGGGA others(13): Show |
4 | a0001c0001t0002g0146a0001c0001t0002g0148a0001c0001t0002g0294others(1): Show | 4 | HG02280.hp1 HG02886.hp2 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.1361-193_1361-192i others(22): Show |
FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 11/13 | INFO_REALIGN_3_PRIME | chr14 | 51721753 | |||||
chr14:51721753
|
A | AGGAGGGA others(21): Show |
98 | a0001c0001t0001g0113a0001c0001t0001g0164a0001c0001t0001g0168others(95): Show | 124 | HG00099.hp2 HG00140.hp2 HG00323.hp2 others(121): Show |
intron_variant | MODIFIER | c.1361-193_1361-192i others(30): Show |
FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 11/13 | INFO_REALIGN_3_PRIME | chr14 | 51721753 | |||||
chr14:51721753
|
A | AGGAGGGA others(29): Show |
1 | a0001c0004t0012g0182 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.1361-193_1361-192i others(38): Show |
FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 11/13 | INFO_REALIGN_3_PRIME | chr14 | 51721753 | |||||
chr14:51721753
|
A | G | 16 | a0001c0002t0001g0196a0001c0004t0001g0046a0001c0004t0001g0063others(13): Show | 16 | HG00280.hp1 HG00639.hp1 HG01109.hp1 others(13): Show |
intron_variant | MODIFIER | c.1361-196A>G | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 11/13 | chr14 | 51721753 | ||||||
chr14:51721759
|
G | GAGGGA | 80 | a0001c0003t0001g0006a0001c0003t0001g0011a0001c0003t0001g0014others(77): Show | 102 | HG00140.hp1 HG00323.hp1 HG00438.hp1 others(99): Show |
intron_variant | MODIFIER | c.1361-186_1361-182d others(7): Show |
FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 11/13 | INFO_REALIGN_3_PRIME | chr14 | 51721759 | |||||
chr14:51721761
|
G | A | 103 | a0001c0001t0001g0113a0001c0001t0001g0164a0001c0001t0001g0168others(100): Show | 129 | HG00099.hp2 HG00140.hp2 HG00323.hp2 others(126): Show |
intron_variant | MODIFIER | c.1361-188G>A | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 11/13 | chr14 | 51721761 | ||||||
chr14:51721777
|
G | C | 1 | a0001c0003t0001g0277 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.1361-172G>C | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 11/13 | chr14 | 51721777 | ||||||
chr14:51722333
|
G | A | 1 | a0001c0003t0001g0040 | 2 | NA19002.hp1 NA19085.hp2 |
intron_variant | MODIFIER | c.1492+253G>A | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 12/13 | chr14 | 51722333 | ||||||
chr14:51722482
|
G | A | 1 | a0001c0002t0008g0016 | 3 | NA18957.hp2 NA18961.hp2 NA19063.hp2 |
intron_variant | MODIFIER | c.1492+402G>A | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 12/13 | chr14 | 51722482 | ||||||
chr14:51722604
|
T | G | 1 | a0001c0015t0001g0242 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.1492+524T>G | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 12/13 | chr14 | 51722604 | ||||||
chr14:51722697
|
C | T | 1 | a0001c0003t0001g0014 | 3 | HG00735.hp2 HG03490.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.1492+617C>T | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 12/13 | chr14 | 51722697 | ||||||
chr14:51723018
|
C | T | 2 | a0002c0008t0009g0072a0002c0008t0009g0291 | 2 | HG02258.hp2 HG02572.hp2 |
intron_variant | MODIFIER | c.1492+938C>T | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 12/13 | chr14 | 51723018 | ||||||
chr14:51723023
|
C | T | 103 | a0001c0001t0001g0113a0001c0001t0001g0164a0001c0001t0001g0168others(100): Show | 129 | HG00099.hp2 HG00140.hp2 HG00323.hp2 others(126): Show |
intron_variant | MODIFIER | c.1492+943C>T | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 12/13 | chr14 | 51723023 | ||||||
chr14:51723071
|
G | A | 103 | a0001c0001t0001g0113a0001c0001t0001g0164a0001c0001t0001g0168others(100): Show | 129 | HG00099.hp2 HG00140.hp2 HG00323.hp2 others(126): Show |
intron_variant | MODIFIER | c.1492+991G>A | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 12/13 | chr14 | 51723071 | ||||||
chr14:51723304
|
A | G | 2 | a0001c0001t0002g0161a0001c0001t0002g0162 | 2 | NA18942.hp2 NA18978.hp2 |
intron_variant | MODIFIER | c.1492+1224A>G | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 12/13 | chr14 | 51723304 | ||||||
chr14:51723504
|
G | T | 4 | a0001c0004t0001g0140a0001c0004t0001g0141a0001c0004t0001g0207others(1): Show | 4 | HG02723.hp2 HG03098.hp1 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.1492+1424G>T | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 12/13 | chr14 | 51723504 | ||||||
chr14:51723623
|
T | A | 103 | a0001c0001t0001g0113a0001c0001t0001g0164a0001c0001t0001g0168others(100): Show | 129 | HG00099.hp2 HG00140.hp2 HG00323.hp2 others(126): Show |
intron_variant | MODIFIER | c.1492+1543T>A | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 12/13 | chr14 | 51723623 | ||||||
chr14:51723624
|
G | T | 103 | a0001c0001t0001g0113a0001c0001t0001g0164a0001c0001t0001g0168others(100): Show | 129 | HG00099.hp2 HG00140.hp2 HG00323.hp2 others(126): Show |
intron_variant | MODIFIER | c.1492+1544G>T | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 12/13 | chr14 | 51723624 | ||||||
chr14:51723625
|
C | A | 103 | a0001c0001t0001g0113a0001c0001t0001g0164a0001c0001t0001g0168others(100): Show | 129 | HG00099.hp2 HG00140.hp2 HG00323.hp2 others(126): Show |
intron_variant | MODIFIER | c.1492+1545C>A | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 12/13 | chr14 | 51723625 | ||||||
chr14:51723625
|
C | CA | 6 | a0001c0002t0001g0039a0001c0002t0001g0085a0001c0002t0001g0091others(3): Show | 7 | NA18954.hp1 NA18978.hp1 NA18994.hp2 others(4): Show |
intron_variant | MODIFIER | c.1492+1557dupA | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 12/13 | INFO_REALIGN_3_PRIME | chr14 | 51723625 | |||||
chr14:51723626
|
A | C | 103 | a0001c0001t0001g0113a0001c0001t0001g0164a0001c0001t0001g0168others(100): Show | 129 | HG00099.hp2 HG00140.hp2 HG00323.hp2 others(126): Show |
intron_variant | MODIFIER | c.1492+1546A>C | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 12/13 | chr14 | 51723626 | ||||||
chr14:51723633
|
A | G | 1 | a0001c0002t0001g0180 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.1492+1553A>G | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 12/13 | chr14 | 51723633 | ||||||
chr14:51723660
|
A | T | 1 | a0001c0001t0002g0315 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.1492+1580A>T | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 12/13 | chr14 | 51723660 | ||||||
chr14:51723721
|
C | G | 103 | a0001c0001t0001g0113a0001c0001t0001g0164a0001c0001t0001g0168others(100): Show | 129 | HG00099.hp2 HG00140.hp2 HG00323.hp2 others(126): Show |
intron_variant | MODIFIER | c.1492+1641C>G | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 12/13 | chr14 | 51723721 | ||||||
chr14:51723731
|
T | C | 103 | a0001c0001t0001g0113a0001c0001t0001g0164a0001c0001t0001g0168others(100): Show | 129 | HG00099.hp2 HG00140.hp2 HG00323.hp2 others(126): Show |
intron_variant | MODIFIER | c.1492+1651T>C | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 12/13 | chr14 | 51723731 | ||||||
chr14:51723772
|
C | CA | 110 | a0001c0001t0001g0113a0001c0001t0001g0164a0001c0001t0001g0168others(107): Show | 137 | HG00099.hp2 HG00140.hp2 HG00323.hp2 others(134): Show |
intron_variant | MODIFIER | c.1492+1706dupA | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 12/13 | INFO_REALIGN_3_PRIME | chr14 | 51723772 | |||||
chr14:51723772
|
CA | C | 101 | a0001c0002t0001g0236a0001c0002t0001g0246a0001c0003t0001g0006others(98): Show | 123 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(120): Show |
intron_variant | MODIFIER | c.1492+1706delA | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 12/13 | INFO_REALIGN_3_PRIME | chr14 | 51723772 | |||||
chr14:51723803
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T | C | 1 | a0001c0003t0001g0194 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1492+1723T>C | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 12/13 | chr14 | 51723803 | ||||||
chr14:51723847
|
C | T | 13 | a0001c0004t0001g0046a0001c0004t0001g0063a0001c0004t0001g0064others(10): Show | 13 | HG00280.hp1 HG00639.hp1 HG01109.hp1 others(10): Show |
intron_variant | MODIFIER | c.1492+1767C>T | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 12/13 | chr14 | 51723847 | ||||||
chr14:51723876
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A | T | 13 | a0001c0004t0001g0046a0001c0004t0001g0063a0001c0004t0001g0064others(10): Show | 13 | HG00280.hp1 HG00639.hp1 HG01109.hp1 others(10): Show |
intron_variant | MODIFIER | c.1492+1796A>T | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 12/13 | chr14 | 51723876 | ||||||
chr14:51723935
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A | G | 4 | a0001c0002t0001g0030a0001c0002t0001g0179a0001c0002t0001g0180others(1): Show | 5 | HG01884.hp2 HG02451.hp2 HG02630.hp2 others(2): Show |
intron_variant | MODIFIER | c.1493-1844A>G | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 12/13 | chr14 | 51723935 | ||||||
chr14:51723957
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A | G | 1 | a0001c0002t0002g0204 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.1493-1822A>G | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 12/13 | chr14 | 51723957 | ||||||
chr14:51724063
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A | G | 4 | a0001c0002t0001g0030a0001c0002t0001g0179a0001c0002t0001g0180others(1): Show | 5 | HG01884.hp2 HG02451.hp2 HG02630.hp2 others(2): Show |
intron_variant | MODIFIER | c.1493-1716A>G | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 12/13 | chr14 | 51724063 | ||||||
chr14:51724097
|
A | G | 1 | a0001c0001t0002g0195 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.1493-1682A>G | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 12/13 | chr14 | 51724097 | ||||||
chr14:51724106
|
C | A | 1 | a0001c0001t0002g0156 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.1493-1673C>A | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 12/13 | chr14 | 51724106 | ||||||
chr14:51724141
|
A | C | 1 | a0005c0016t0002g0106 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.1493-1638A>C | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 12/13 | chr14 | 51724141 | ||||||
chr14:51724209
|
T | TA | 6 | a0001c0001t0002g0109a0001c0001t0002g0157a0001c0002t0001g0074others(3): Show | 6 | HG03688.hp1 NA18961.hp1 NA18967.hp1 others(3): Show |
intron_variant | MODIFIER | c.1493-1556dupA | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 12/13 | INFO_REALIGN_3_PRIME | chr14 | 51724209 | |||||
chr14:51724209
|
TA | T | 4 | a0001c0001t0002g0315a0001c0003t0001g0015a0001c0003t0001g0263others(1): Show | 6 | HG01081.hp2 HG01106.hp2 HG01167.hp1 others(3): Show |
intron_variant | MODIFIER | c.1493-1556delA | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 12/13 | INFO_REALIGN_3_PRIME | chr14 | 51724209 | |||||
chr14:51724374
|
A | C | 3 | a0001c0003t0001g0138a0001c0003t0001g0280a0001c0003t0001g0299 | 3 | NA18941.hp1 NA19000.hp2 NA19066.hp2 |
intron_variant | MODIFIER | c.1493-1405A>C | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 12/13 | chr14 | 51724374 | ||||||
chr14:51724731
|
G | GT | 83 | a0001c0001t0001g0113a0001c0002t0001g0166a0001c0003t0001g0006others(80): Show | 105 | HG00140.hp1 HG00323.hp1 HG00438.hp1 others(102): Show |
intron_variant | MODIFIER | c.1493-1036dupT | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 12/13 | INFO_REALIGN_3_PRIME | chr14 | 51724731 | |||||
chr14:51724731
|
G | T | 1 | a0001c0003t0001g0279 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.1493-1048G>T | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 12/13 | chr14 | 51724731 | ||||||
chr14:51724763
|
T | C | 81 | a0001c0002t0001g0166a0001c0003t0001g0006a0001c0003t0001g0011others(78): Show | 103 | HG00140.hp1 HG00323.hp1 HG00438.hp1 others(100): Show |
intron_variant | MODIFIER | c.1493-1016T>C | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 12/13 | chr14 | 51724763 | ||||||
chr14:51724941
|
C | G | 1 | a0001c0001t0024g0124 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.1493-838C>G | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 12/13 | chr14 | 51724941 | ||||||
chr14:51724972
|
A | G | 4 | a0001c0004t0005g0185a0001c0004t0005g0187a0001c0004t0005g0190others(1): Show | 4 | HG02083.hp2 NA18994.hp2 NA19055.hp1 others(1): Show |
intron_variant | MODIFIER | c.1493-807A>G | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 12/13 | chr14 | 51724972 | ||||||
chr14:51725581
|
A | G | 2 | a0001c0002t0001g0150a0001c0002t0001g0215 | 2 | HG02559.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.1493-198A>G | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 12/13 | chr14 | 51725581 | ||||||
chr14:51725766
|
T | G | 1 | a0001c0001t0002g0170 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.1493-13T>G | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 12/13 | chr14 | 51725766 | ||||||
chr14:51726047
|
T | C | 3 | a0001c0001t0006g0019a0001c0001t0006g0059a0001c0001t0023g0058 | 4 | HG01261.hp1 HG02965.hp2 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.1584+177T>C | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 13/13 | chr14 | 51726047 | ||||||
chr14:51726074
|
T | C | 103 | a0001c0001t0001g0113a0001c0001t0001g0164a0001c0001t0001g0168others(100): Show | 129 | HG00099.hp2 HG00140.hp2 HG00323.hp2 others(126): Show |
intron_variant | MODIFIER | c.1584+204T>C | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 13/13 | chr14 | 51726074 | ||||||
chr14:51726085
|
T | C | 1 | a0001c0001t0002g0231 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.1584+215T>C | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 13/13 | chr14 | 51726085 | ||||||
chr14:51726695
|
C | T | 3 | a0001c0001t0011g0131a0001c0001t0011g0132a0001c0001t0024g0124 | 3 | HG02896.hp2 HG02897.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.1584+825C>T | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 13/13 | chr14 | 51726695 | ||||||
chr14:51726842
|
C | T | 2 | a0001c0001t0002g0054a0001c0001t0002g0114 | 2 | HG01891.hp1 HG02895.hp1 |
intron_variant | MODIFIER | c.1585-903C>T | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 13/13 | chr14 | 51726842 | ||||||
chr14:51727021
|
G | C | 1 | a0001c0002t0002g0204 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.1585-724G>C | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 13/13 | chr14 | 51727021 | ||||||
chr14:51727027
|
T | TA | 9 | a0001c0006t0003g0027a0001c0006t0003g0151a0001c0006t0003g0152others(6): Show | 10 | HG01358.hp1 HG01433.hp1 HG02145.hp2 others(7): Show |
intron_variant | MODIFIER | c.1585-710dupA | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 13/13 | INFO_REALIGN_3_PRIME | chr14 | 51727027 | |||||
chr14:51727027
|
TA | T | 19 | a0001c0001t0002g0105a0001c0003t0001g0006a0001c0003t0001g0017others(16): Show | 25 | HG01070.hp2 HG01071.hp1 HG01123.hp1 others(22): Show |
intron_variant | MODIFIER | c.1585-710delA | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 13/13 | INFO_REALIGN_3_PRIME | chr14 | 51727027 | |||||
chr14:51727042
|
C | T | 1 | a0001c0004t0001g0035 | 2 | HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.1585-703C>T | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 13/13 | chr14 | 51727042 | ||||||
chr14:51727083
|
G | A | 1 | a0001c0003t0001g0283 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.1585-662G>A | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 13/13 | chr14 | 51727083 | ||||||
chr14:51727094
|
G | A | 5 | a0001c0001t0002g0020a0001c0001t0002g0049a0001c0001t0002g0158others(2): Show | 6 | HG00099.hp2 HG00639.hp2 HG01516.hp1 others(3): Show |
intron_variant | MODIFIER | c.1585-651G>A | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 13/13 | chr14 | 51727094 | ||||||
chr14:51727309
|
G | GA | 96 | a0001c0001t0001g0113a0001c0001t0002g0001a0001c0001t0002g0002others(93): Show | 122 | HG00099.hp2 HG00140.hp2 HG00544.hp1 others(119): Show |
intron_variant | MODIFIER | c.1585-425dupA | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 13/13 | INFO_REALIGN_3_PRIME | chr14 | 51727309 | |||||
chr14:51727489
|
G | A | 101 | a0001c0001t0001g0113a0001c0001t0002g0001a0001c0001t0002g0002others(98): Show | 127 | HG00099.hp2 HG00140.hp2 HG00544.hp1 others(124): Show |
intron_variant | MODIFIER | c.1585-256G>A | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 13/13 | chr14 | 51727489 | ||||||
chr14:51727689
|
G | A | 101 | a0001c0001t0001g0113a0001c0001t0002g0001a0001c0001t0002g0002others(98): Show | 127 | HG00099.hp2 HG00140.hp2 HG00544.hp1 others(124): Show |
intron_variant | MODIFIER | c.1585-56G>A | FRMD6 | ENSG00000139926.16 | transcript | ENST00000344768.10 | protein_coding | 13/13 | chr14 | 51727689 |