geneid | 2335 |
---|---|
ensemblid | ENSG00000115414.21 |
hgncid | 3778 |
symbol | FN1 |
name | fibronectin 1 |
refseq_nuc | NM_212482.4 |
refseq_prot | NP_997647.2 |
ensembl_nuc | ENST00000354785.11 |
ensembl_prot | ENSP00000346839.4 |
mane_status | MANE Select |
chr | chr2 |
start | 215360865 |
end | 215436068 |
strand | - |
ver | v1.2 |
region | chr2:215360865-215436068 |
region5000 | chr2:215355865-215441068 |
regionname0 | FN1_chr2_215360865_215436068 |
regionname5000 | FN1_chr2_215355865_215441068 |
ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 0/1 | 2477 | 150 | 56 | 44 | 20 | 10 | 19 | 9 | FN1_chr2_215355865_215441068 | FN1 | copy fasta | chr2 | 215355865 | 215441068 |
a0002 | 0/0 | 2477 | 47 | 7 | 16 | 9 | 4 | 11 | 6 | FN1_chr2_215355865_215441068 | FN1 | copy fasta | chr2 | 215355865 | 215441068 |
a0003 | 0/0 | 2477 | 11 | 11 | 0 | 0 | 0 | 0 | 0 | FN1_chr2_215355865_215441068 | FN1 | copy fasta | chr2 | 215355865 | 215441068 |
a0004 | 0/0 | 2477 | 4 | 4 | 0 | 0 | 0 | 0 | 0 | FN1_chr2_215355865_215441068 | FN1 | copy fasta | chr2 | 215355865 | 215441068 |
a0005 | 0/0 | 2477 | 3 | 3 | 0 | 0 | 0 | 0 | 0 | FN1_chr2_215355865_215441068 | FN1 | copy fasta | chr2 | 215355865 | 215441068 |
a0006 | 0/0 | 2477 | 3 | 3 | 0 | 0 | 0 | 0 | 0 | FN1_chr2_215355865_215441068 | FN1 | copy fasta | chr2 | 215355865 | 215441068 |
a0007 | 0/0 | 2477 | 3 | 2 | 1 | 0 | 0 | 0 | 0 | FN1_chr2_215355865_215441068 | FN1 | copy fasta | chr2 | 215355865 | 215441068 |
a0008 | 0/0 | 2477 | 3 | 0 | 2 | 0 | 0 | 1 | 0 | FN1_chr2_215355865_215441068 | FN1 | copy fasta | chr2 | 215355865 | 215441068 |
a0009 | 0/0 | 2477 | 3 | 0 | 3 | 0 | 0 | 0 | 0 | FN1_chr2_215355865_215441068 | FN1 | copy fasta | chr2 | 215355865 | 215441068 |
a0010 | 0/0 | 2477 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | FN1_chr2_215355865_215441068 | FN1 | copy fasta | chr2 | 215355865 | 215441068 |
a0011 | 0/0 | 2477 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | FN1_chr2_215355865_215441068 | FN1 | copy fasta | chr2 | 215355865 | 215441068 |
a0012 | 0/0 | 2477 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | FN1_chr2_215355865_215441068 | FN1 | copy fasta | chr2 | 215355865 | 215441068 |
a0013 | 0/0 | 2477 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | FN1_chr2_215355865_215441068 | FN1 | copy fasta | chr2 | 215355865 | 215441068 |
a0014 | 0/0 | 2477 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | FN1_chr2_215355865_215441068 | FN1 | copy fasta | chr2 | 215355865 | 215441068 |
a0015 | 0/0 | 2477 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | FN1_chr2_215355865_215441068 | FN1 | copy fasta | chr2 | 215355865 | 215441068 |
a0016 | 0/0 | 2477 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | FN1_chr2_215355865_215441068 | FN1 | copy fasta | chr2 | 215355865 | 215441068 |
a0017 | 0/0 | 2477 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | FN1_chr2_215355865_215441068 | FN1 | copy fasta | chr2 | 215355865 | 215441068 |
a0018 | 0/0 | 2477 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | FN1_chr2_215355865_215441068 | FN1 | copy fasta | chr2 | 215355865 | 215441068 |
a0019 | 0/0 | 2477 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | FN1_chr2_215355865_215441068 | FN1 | copy fasta | chr2 | 215355865 | 215441068 |
a0020 | 1/0 | 2477 | 1 | 0 | 0 | 0 | 0 | 0 | 0 | FN1_chr2_215355865_215441068 | FN1 | copy fasta | chr2 | 215355865 | 215441068 |
chapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
c0001 | 0/0 | 7434 | 39 | 2 | 15 | 14 | 2 | 6 | FN1_chr2_215355865_215441068 | FN1 | copy fasta | chr2 | 215355865 | 215441068 |
c0002 | 0/1 | 7434 | 28 | 15 | 7 | 0 | 2 | 3 | FN1_chr2_215355865_215441068 | FN1 | copy fasta | chr2 | 215355865 | 215441068 |
c0003 | 0/0 | 7434 | 19 | 0 | 6 | 5 | 1 | 7 | FN1_chr2_215355865_215441068 | FN1 | copy fasta | chr2 | 215355865 | 215441068 |
c0004 | 0/0 | 7434 | 13 | 2 | 6 | 0 | 0 | 5 | FN1_chr2_215355865_215441068 | FN1 | copy fasta | chr2 | 215355865 | 215441068 |
c0005 | 0/0 | 7434 | 12 | 7 | 3 | 1 | 0 | 1 | FN1_chr2_215355865_215441068 | FN1 | copy fasta | chr2 | 215355865 | 215441068 |
c0006 | 0/0 | 7434 | 12 | 8 | 3 | 0 | 1 | 0 | FN1_chr2_215355865_215441068 | FN1 | copy fasta | chr2 | 215355865 | 215441068 |
c0007 | 0/0 | 7434 | 9 | 9 | 0 | 0 | 0 | 0 | FN1_chr2_215355865_215441068 | FN1 | copy fasta | chr2 | 215355865 | 215441068 |
c0008 | 0/0 | 7434 | 8 | 0 | 4 | 2 | 1 | 1 | FN1_chr2_215355865_215441068 | FN1 | copy fasta | chr2 | 215355865 | 215441068 |
c0009 | 0/0 | 7434 | 6 | 6 | 0 | 0 | 0 | 0 | FN1_chr2_215355865_215441068 | FN1 | copy fasta | chr2 | 215355865 | 215441068 |
c0010 | 0/0 | 7434 | 5 | 0 | 2 | 3 | 0 | 0 | FN1_chr2_215355865_215441068 | FN1 | copy fasta | chr2 | 215355865 | 215441068 |
c0011 | 0/0 | 7434 | 5 | 0 | 3 | 0 | 1 | 1 | FN1_chr2_215355865_215441068 | FN1 | copy fasta | chr2 | 215355865 | 215441068 |
c0012 | 0/0 | 7434 | 5 | 1 | 1 | 0 | 2 | 1 | FN1_chr2_215355865_215441068 | FN1 | copy fasta | chr2 | 215355865 | 215441068 |
c0013 | 0/0 | 7434 | 4 | 1 | 2 | 1 | 0 | 0 | FN1_chr2_215355865_215441068 | FN1 | copy fasta | chr2 | 215355865 | 215441068 |
c0014 | 0/0 | 7434 | 4 | 3 | 1 | 0 | 0 | 0 | FN1_chr2_215355865_215441068 | FN1 | copy fasta | chr2 | 215355865 | 215441068 |
c0015 | 0/0 | 7434 | 4 | 4 | 0 | 0 | 0 | 0 | FN1_chr2_215355865_215441068 | FN1 | copy fasta | chr2 | 215355865 | 215441068 |
c0016 | 0/0 | 7434 | 3 | 0 | 3 | 0 | 0 | 0 | FN1_chr2_215355865_215441068 | FN1 | copy fasta | chr2 | 215355865 | 215441068 |
c0017 | 0/0 | 7434 | 3 | 2 | 1 | 0 | 0 | 0 | FN1_chr2_215355865_215441068 | FN1 | copy fasta | chr2 | 215355865 | 215441068 |
c0018 | 0/0 | 7434 | 3 | 0 | 2 | 0 | 0 | 1 | FN1_chr2_215355865_215441068 | FN1 | copy fasta | chr2 | 215355865 | 215441068 |
c0019 | 0/0 | 7434 | 2 | 2 | 0 | 0 | 0 | 0 | FN1_chr2_215355865_215441068 | FN1 | copy fasta | chr2 | 215355865 | 215441068 |
c0020 | 0/0 | 7434 | 2 | 2 | 0 | 0 | 0 | 0 | FN1_chr2_215355865_215441068 | FN1 | copy fasta | chr2 | 215355865 | 215441068 |
c0021 | 0/0 | 7434 | 2 | 0 | 1 | 0 | 1 | 0 | FN1_chr2_215355865_215441068 | FN1 | copy fasta | chr2 | 215355865 | 215441068 |
c0022 | 0/0 | 7434 | 2 | 0 | 1 | 0 | 0 | 1 | FN1_chr2_215355865_215441068 | FN1 | copy fasta | chr2 | 215355865 | 215441068 |
c0023 | 0/0 | 7434 | 2 | 2 | 0 | 0 | 0 | 0 | FN1_chr2_215355865_215441068 | FN1 | copy fasta | chr2 | 215355865 | 215441068 |
c0024 | 0/0 | 7434 | 2 | 2 | 0 | 0 | 0 | 0 | FN1_chr2_215355865_215441068 | FN1 | copy fasta | chr2 | 215355865 | 215441068 |
c0025 | 0/0 | 7434 | 2 | 2 | 0 | 0 | 0 | 0 | FN1_chr2_215355865_215441068 | FN1 | copy fasta | chr2 | 215355865 | 215441068 |
c0026 | 0/0 | 7434 | 2 | 2 | 0 | 0 | 0 | 0 | FN1_chr2_215355865_215441068 | FN1 | copy fasta | chr2 | 215355865 | 215441068 |
c0027 | 0/0 | 7434 | 2 | 0 | 1 | 0 | 1 | 0 | FN1_chr2_215355865_215441068 | FN1 | copy fasta | chr2 | 215355865 | 215441068 |
c0028 | 0/0 | 7434 | 2 | 2 | 0 | 0 | 0 | 0 | FN1_chr2_215355865_215441068 | FN1 | copy fasta | chr2 | 215355865 | 215441068 |
c0029 | 0/0 | 7434 | 2 | 2 | 0 | 0 | 0 | 0 | FN1_chr2_215355865_215441068 | FN1 | copy fasta | chr2 | 215355865 | 215441068 |
c0030 | 0/0 | 7434 | 1 | 0 | 0 | 0 | 1 | 0 | FN1_chr2_215355865_215441068 | FN1 | copy fasta | chr2 | 215355865 | 215441068 |
c0031 | 0/0 | 7434 | 1 | 0 | 1 | 0 | 0 | 0 | FN1_chr2_215355865_215441068 | FN1 | copy fasta | chr2 | 215355865 | 215441068 |
c0032 | 0/0 | 7434 | 1 | 0 | 0 | 1 | 0 | 0 | FN1_chr2_215355865_215441068 | FN1 | copy fasta | chr2 | 215355865 | 215441068 |
c0033 | 0/0 | 7434 | 1 | 0 | 0 | 0 | 0 | 1 | FN1_chr2_215355865_215441068 | FN1 | copy fasta | chr2 | 215355865 | 215441068 |
c0034 | 0/0 | 7434 | 1 | 0 | 0 | 0 | 0 | 1 | FN1_chr2_215355865_215441068 | FN1 | copy fasta | chr2 | 215355865 | 215441068 |
c0035 | 1/0 | 7434 | 1 | 0 | 0 | 0 | 0 | 0 | FN1_chr2_215355865_215441068 | FN1 | copy fasta | chr2 | 215355865 | 215441068 |
c0036 | 0/0 | 7434 | 1 | 0 | 0 | 0 | 0 | 1 | FN1_chr2_215355865_215441068 | FN1 | copy fasta | chr2 | 215355865 | 215441068 |
c0037 | 0/0 | 7434 | 1 | 1 | 0 | 0 | 0 | 0 | FN1_chr2_215355865_215441068 | FN1 | copy fasta | chr2 | 215355865 | 215441068 |
c0038 | 0/0 | 7434 | 1 | 1 | 0 | 0 | 0 | 0 | FN1_chr2_215355865_215441068 | FN1 | copy fasta | chr2 | 215355865 | 215441068 |
c0039 | 0/0 | 7434 | 1 | 0 | 0 | 0 | 0 | 1 | FN1_chr2_215355865_215441068 | FN1 | copy fasta | chr2 | 215355865 | 215441068 |
c0040 | 0/0 | 7434 | 1 | 1 | 0 | 0 | 0 | 0 | FN1_chr2_215355865_215441068 | FN1 | copy fasta | chr2 | 215355865 | 215441068 |
c0041 | 0/0 | 7434 | 1 | 1 | 0 | 0 | 0 | 0 | FN1_chr2_215355865_215441068 | FN1 | copy fasta | chr2 | 215355865 | 215441068 |
c0042 | 0/0 | 7434 | 1 | 1 | 0 | 0 | 0 | 0 | FN1_chr2_215355865_215441068 | FN1 | copy fasta | chr2 | 215355865 | 215441068 |
c0043 | 0/0 | 7434 | 1 | 0 | 0 | 1 | 0 | 0 | FN1_chr2_215355865_215441068 | FN1 | copy fasta | chr2 | 215355865 | 215441068 |
c0044 | 0/0 | 7434 | 1 | 1 | 0 | 0 | 0 | 0 | FN1_chr2_215355865_215441068 | FN1 | copy fasta | chr2 | 215355865 | 215441068 |
c0045 | 0/0 | 7434 | 1 | 1 | 0 | 0 | 0 | 0 | FN1_chr2_215355865_215441068 | FN1 | copy fasta | chr2 | 215355865 | 215441068 |
c0046 | 0/0 | 7434 | 1 | 1 | 0 | 0 | 0 | 0 | FN1_chr2_215355865_215441068 | FN1 | copy fasta | chr2 | 215355865 | 215441068 |
c0047 | 0/0 | 7434 | 1 | 0 | 0 | 1 | 0 | 0 | FN1_chr2_215355865_215441068 | FN1 | copy fasta | chr2 | 215355865 | 215441068 |
c0048 | 0/0 | 7434 | 1 | 1 | 0 | 0 | 0 | 0 | FN1_chr2_215355865_215441068 | FN1 | copy fasta | chr2 | 215355865 | 215441068 |
c0049 | 0/0 | 7434 | 1 | 0 | 0 | 0 | 0 | 1 | FN1_chr2_215355865_215441068 | FN1 | copy fasta | chr2 | 215355865 | 215441068 |
c0050 | 0/0 | 7434 | 1 | 0 | 0 | 1 | 0 | 0 | FN1_chr2_215355865_215441068 | FN1 | copy fasta | chr2 | 215355865 | 215441068 |
c0051 | 0/0 | 7434 | 1 | 0 | 0 | 0 | 1 | 0 | FN1_chr2_215355865_215441068 | FN1 | copy fasta | chr2 | 215355865 | 215441068 |
c0052 | 0/0 | 7434 | 1 | 0 | 0 | 0 | 0 | 1 | FN1_chr2_215355865_215441068 | FN1 | copy fasta | chr2 | 215355865 | 215441068 |
c0053 | 0/0 | 7434 | 1 | 0 | 0 | 1 | 0 | 0 | FN1_chr2_215355865_215441068 | FN1 | copy fasta | chr2 | 215355865 | 215441068 |
c0054 | 0/0 | 7434 | 1 | 0 | 0 | 1 | 0 | 0 | FN1_chr2_215355865_215441068 | FN1 | copy fasta | chr2 | 215355865 | 215441068 |
c0055 | 0/0 | 7434 | 1 | 1 | 0 | 0 | 0 | 0 | FN1_chr2_215355865_215441068 | FN1 | copy fasta | chr2 | 215355865 | 215441068 |
c0056 | 0/0 | 7434 | 1 | 1 | 0 | 0 | 0 | 0 | FN1_chr2_215355865_215441068 | FN1 | copy fasta | chr2 | 215355865 | 215441068 |
c0057 | 0/0 | 7434 | 1 | 0 | 0 | 0 | 0 | 1 | FN1_chr2_215355865_215441068 | FN1 | copy fasta | chr2 | 215355865 | 215441068 |
c0058 | 0/0 | 7434 | 1 | 1 | 0 | 0 | 0 | 0 | FN1_chr2_215355865_215441068 | FN1 | copy fasta | chr2 | 215355865 | 215441068 |
c0059 | 0/0 | 7434 | 1 | 0 | 1 | 0 | 0 | 0 | FN1_chr2_215355865_215441068 | FN1 | copy fasta | chr2 | 215355865 | 215441068 |
c0060 | 0/0 | 7434 | 1 | 1 | 0 | 0 | 0 | 0 | FN1_chr2_215355865_215441068 | FN1 | copy fasta | chr2 | 215355865 | 215441068 |
c0061 | 0/0 | 7434 | 1 | 1 | 0 | 0 | 0 | 0 | FN1_chr2_215355865_215441068 | FN1 | copy fasta | chr2 | 215355865 | 215441068 |
c0062 | 0/0 | 7434 | 1 | 1 | 0 | 0 | 0 | 0 | FN1_chr2_215355865_215441068 | FN1 | copy fasta | chr2 | 215355865 | 215441068 |
c0063 | 0/0 | 7434 | 1 | 0 | 1 | 0 | 0 | 0 | FN1_chr2_215355865_215441068 | FN1 | copy fasta | chr2 | 215355865 | 215441068 |
c0064 | 0/0 | 7434 | 1 | 0 | 1 | 0 | 0 | 0 | FN1_chr2_215355865_215441068 | FN1 | copy fasta | chr2 | 215355865 | 215441068 |
c0065 | 0/0 | 7434 | 1 | 1 | 0 | 0 | 0 | 0 | FN1_chr2_215355865_215441068 | FN1 | copy fasta | chr2 | 215355865 | 215441068 |
thapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
t0001 | 1/1 | 957 | 215 | 67 | 66 | 32 | 14 | 34 | FN1_chr2_215355865_215441068 | FN1 | copy fasta | chr2 | 215355865 | 215441068 |
t0002 | 0/0 | 957 | 17 | 17 | 0 | 0 | 0 | 0 | FN1_chr2_215355865_215441068 | FN1 | copy fasta | chr2 | 215355865 | 215441068 |
t0003 | 0/0 | 957 | 7 | 7 | 0 | 0 | 0 | 0 | FN1_chr2_215355865_215441068 | FN1 | copy fasta | chr2 | 215355865 | 215441068 |
t0004 | 0/0 | 957 | 1 | 1 | 0 | 0 | 0 | 0 | FN1_chr2_215355865_215441068 | FN1 | copy fasta | chr2 | 215355865 | 215441068 |
ghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
g0001 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | FN1_chr2_215355865_215441068 | FN1 | chr2 | 215355865 | 215441068 |
g0002 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | FN1_chr2_215355865_215441068 | FN1 | chr2 | 215355865 | 215441068 |
g0003 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FN1_chr2_215355865_215441068 | FN1 | chr2 | 215355865 | 215441068 |
g0004 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FN1_chr2_215355865_215441068 | FN1 | chr2 | 215355865 | 215441068 |
g0005 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FN1_chr2_215355865_215441068 | FN1 | chr2 | 215355865 | 215441068 |
g0006 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FN1_chr2_215355865_215441068 | FN1 | chr2 | 215355865 | 215441068 |
g0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FN1_chr2_215355865_215441068 | FN1 | chr2 | 215355865 | 215441068 |
g0008 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FN1_chr2_215355865_215441068 | FN1 | chr2 | 215355865 | 215441068 |
g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FN1_chr2_215355865_215441068 | FN1 | chr2 | 215355865 | 215441068 |
g0010 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FN1_chr2_215355865_215441068 | FN1 | chr2 | 215355865 | 215441068 |
g0011 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FN1_chr2_215355865_215441068 | FN1 | chr2 | 215355865 | 215441068 |
g0012 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FN1_chr2_215355865_215441068 | FN1 | chr2 | 215355865 | 215441068 |
g0013 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FN1_chr2_215355865_215441068 | FN1 | chr2 | 215355865 | 215441068 |
g0014 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FN1_chr2_215355865_215441068 | FN1 | chr2 | 215355865 | 215441068 |
g0015 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FN1_chr2_215355865_215441068 | FN1 | chr2 | 215355865 | 215441068 |
g0016 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FN1_chr2_215355865_215441068 | FN1 | chr2 | 215355865 | 215441068 |
g0017 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FN1_chr2_215355865_215441068 | FN1 | chr2 | 215355865 | 215441068 |
g0018 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FN1_chr2_215355865_215441068 | FN1 | chr2 | 215355865 | 215441068 |
g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FN1_chr2_215355865_215441068 | FN1 | chr2 | 215355865 | 215441068 |
g0020 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | FN1_chr2_215355865_215441068 | FN1 | chr2 | 215355865 | 215441068 |
g0021 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FN1_chr2_215355865_215441068 | FN1 | chr2 | 215355865 | 215441068 |
g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FN1_chr2_215355865_215441068 | FN1 | chr2 | 215355865 | 215441068 |
g0023 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FN1_chr2_215355865_215441068 | FN1 | chr2 | 215355865 | 215441068 |
g0024 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FN1_chr2_215355865_215441068 | FN1 | chr2 | 215355865 | 215441068 |
g0025 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FN1_chr2_215355865_215441068 | FN1 | chr2 | 215355865 | 215441068 |
g0026 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FN1_chr2_215355865_215441068 | FN1 | chr2 | 215355865 | 215441068 |
g0027 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FN1_chr2_215355865_215441068 | FN1 | chr2 | 215355865 | 215441068 |
g0028 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FN1_chr2_215355865_215441068 | FN1 | chr2 | 215355865 | 215441068 |
g0029 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FN1_chr2_215355865_215441068 | FN1 | chr2 | 215355865 | 215441068 |
g0030 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FN1_chr2_215355865_215441068 | FN1 | chr2 | 215355865 | 215441068 |
g0031 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FN1_chr2_215355865_215441068 | FN1 | chr2 | 215355865 | 215441068 |
g0032 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FN1_chr2_215355865_215441068 | FN1 | chr2 | 215355865 | 215441068 |
g0033 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FN1_chr2_215355865_215441068 | FN1 | chr2 | 215355865 | 215441068 |
g0034 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FN1_chr2_215355865_215441068 | FN1 | chr2 | 215355865 | 215441068 |
g0035 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FN1_chr2_215355865_215441068 | FN1 | chr2 | 215355865 | 215441068 |
g0036 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FN1_chr2_215355865_215441068 | FN1 | chr2 | 215355865 | 215441068 |
g0037 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FN1_chr2_215355865_215441068 | FN1 | chr2 | 215355865 | 215441068 |
g0038 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FN1_chr2_215355865_215441068 | FN1 | chr2 | 215355865 | 215441068 |
g0039 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FN1_chr2_215355865_215441068 | FN1 | chr2 | 215355865 | 215441068 |
g0040 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FN1_chr2_215355865_215441068 | FN1 | chr2 | 215355865 | 215441068 |
g0041 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FN1_chr2_215355865_215441068 | FN1 | chr2 | 215355865 | 215441068 |
g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FN1_chr2_215355865_215441068 | FN1 | chr2 | 215355865 | 215441068 |
g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FN1_chr2_215355865_215441068 | FN1 | chr2 | 215355865 | 215441068 |
g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FN1_chr2_215355865_215441068 | FN1 | chr2 | 215355865 | 215441068 |
g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FN1_chr2_215355865_215441068 | FN1 | chr2 | 215355865 | 215441068 |
g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FN1_chr2_215355865_215441068 | FN1 | chr2 | 215355865 | 215441068 |
g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FN1_chr2_215355865_215441068 | FN1 | chr2 | 215355865 | 215441068 |
g0048 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FN1_chr2_215355865_215441068 | FN1 | chr2 | 215355865 | 215441068 |
g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FN1_chr2_215355865_215441068 | FN1 | chr2 | 215355865 | 215441068 |
g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FN1_chr2_215355865_215441068 | FN1 | chr2 | 215355865 | 215441068 |
g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FN1_chr2_215355865_215441068 | FN1 | chr2 | 215355865 | 215441068 |
g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FN1_chr2_215355865_215441068 | FN1 | chr2 | 215355865 | 215441068 |
g0053 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FN1_chr2_215355865_215441068 | FN1 | chr2 | 215355865 | 215441068 |
g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FN1_chr2_215355865_215441068 | FN1 | chr2 | 215355865 | 215441068 |
g0055 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FN1_chr2_215355865_215441068 | FN1 | chr2 | 215355865 | 215441068 |
g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FN1_chr2_215355865_215441068 | FN1 | chr2 | 215355865 | 215441068 |
g0057 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FN1_chr2_215355865_215441068 | FN1 | chr2 | 215355865 | 215441068 |
g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FN1_chr2_215355865_215441068 | FN1 | chr2 | 215355865 | 215441068 |
g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FN1_chr2_215355865_215441068 | FN1 | chr2 | 215355865 | 215441068 |
g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FN1_chr2_215355865_215441068 | FN1 | chr2 | 215355865 | 215441068 |
g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FN1_chr2_215355865_215441068 | FN1 | chr2 | 215355865 | 215441068 |
g0062 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FN1_chr2_215355865_215441068 | FN1 | chr2 | 215355865 | 215441068 |
g0063 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FN1_chr2_215355865_215441068 | FN1 | chr2 | 215355865 | 215441068 |
g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FN1_chr2_215355865_215441068 | FN1 | chr2 | 215355865 | 215441068 |
g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FN1_chr2_215355865_215441068 | FN1 | chr2 | 215355865 | 215441068 |
g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FN1_chr2_215355865_215441068 | FN1 | chr2 | 215355865 | 215441068 |
g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FN1_chr2_215355865_215441068 | FN1 | chr2 | 215355865 | 215441068 |
g0068 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FN1_chr2_215355865_215441068 | FN1 | chr2 | 215355865 | 215441068 |
g0069 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FN1_chr2_215355865_215441068 | FN1 | chr2 | 215355865 | 215441068 |
g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FN1_chr2_215355865_215441068 | FN1 | chr2 | 215355865 | 215441068 |
g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FN1_chr2_215355865_215441068 | FN1 | chr2 | 215355865 | 215441068 |
g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FN1_chr2_215355865_215441068 | FN1 | chr2 | 215355865 | 215441068 |
g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FN1_chr2_215355865_215441068 | FN1 | chr2 | 215355865 | 215441068 |
g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FN1_chr2_215355865_215441068 | FN1 | chr2 | 215355865 | 215441068 |
g0075 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FN1_chr2_215355865_215441068 | FN1 | chr2 | 215355865 | 215441068 |
g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FN1_chr2_215355865_215441068 | FN1 | chr2 | 215355865 | 215441068 |
g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FN1_chr2_215355865_215441068 | FN1 | chr2 | 215355865 | 215441068 |
g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FN1_chr2_215355865_215441068 | FN1 | chr2 | 215355865 | 215441068 |
g0079 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FN1_chr2_215355865_215441068 | FN1 | chr2 | 215355865 | 215441068 |
g0080 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FN1_chr2_215355865_215441068 | FN1 | chr2 | 215355865 | 215441068 |
g0081 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FN1_chr2_215355865_215441068 | FN1 | chr2 | 215355865 | 215441068 |
g0082 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FN1_chr2_215355865_215441068 | FN1 | chr2 | 215355865 | 215441068 |
g0083 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FN1_chr2_215355865_215441068 | FN1 | chr2 | 215355865 | 215441068 |
g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FN1_chr2_215355865_215441068 | FN1 | chr2 | 215355865 | 215441068 |
g0085 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FN1_chr2_215355865_215441068 | FN1 | chr2 | 215355865 | 215441068 |
g0086 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FN1_chr2_215355865_215441068 | FN1 | chr2 | 215355865 | 215441068 |
g0087 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FN1_chr2_215355865_215441068 | FN1 | chr2 | 215355865 | 215441068 |
g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FN1_chr2_215355865_215441068 | FN1 | chr2 | 215355865 | 215441068 |
g0089 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FN1_chr2_215355865_215441068 | FN1 | chr2 | 215355865 | 215441068 |
g0090 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FN1_chr2_215355865_215441068 | FN1 | chr2 | 215355865 | 215441068 |
g0091 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FN1_chr2_215355865_215441068 | FN1 | chr2 | 215355865 | 215441068 |
g0092 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FN1_chr2_215355865_215441068 | FN1 | chr2 | 215355865 | 215441068 |
g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FN1_chr2_215355865_215441068 | FN1 | chr2 | 215355865 | 215441068 |
g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FN1_chr2_215355865_215441068 | FN1 | chr2 | 215355865 | 215441068 |
g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FN1_chr2_215355865_215441068 | FN1 | chr2 | 215355865 | 215441068 |
g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FN1_chr2_215355865_215441068 | FN1 | chr2 | 215355865 | 215441068 |
g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FN1_chr2_215355865_215441068 | FN1 | chr2 | 215355865 | 215441068 |
g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FN1_chr2_215355865_215441068 | FN1 | chr2 | 215355865 | 215441068 |
g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FN1_chr2_215355865_215441068 | FN1 | chr2 | 215355865 | 215441068 |
g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FN1_chr2_215355865_215441068 | FN1 | chr2 | 215355865 | 215441068 |
g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FN1_chr2_215355865_215441068 | FN1 | chr2 | 215355865 | 215441068 |
g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FN1_chr2_215355865_215441068 | FN1 | chr2 | 215355865 | 215441068 |
g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FN1_chr2_215355865_215441068 | FN1 | chr2 | 215355865 | 215441068 |
g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FN1_chr2_215355865_215441068 | FN1 | chr2 | 215355865 | 215441068 |
g0105 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FN1_chr2_215355865_215441068 | FN1 | chr2 | 215355865 | 215441068 |
g0106 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FN1_chr2_215355865_215441068 | FN1 | chr2 | 215355865 | 215441068 |
g0107 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FN1_chr2_215355865_215441068 | FN1 | chr2 | 215355865 | 215441068 |
g0108 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FN1_chr2_215355865_215441068 | FN1 | chr2 | 215355865 | 215441068 |
g0109 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FN1_chr2_215355865_215441068 | FN1 | chr2 | 215355865 | 215441068 |
g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FN1_chr2_215355865_215441068 | FN1 | chr2 | 215355865 | 215441068 |
g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FN1_chr2_215355865_215441068 | FN1 | chr2 | 215355865 | 215441068 |
g0112 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FN1_chr2_215355865_215441068 | FN1 | chr2 | 215355865 | 215441068 |
g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FN1_chr2_215355865_215441068 | FN1 | chr2 | 215355865 | 215441068 |
g0114 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FN1_chr2_215355865_215441068 | FN1 | chr2 | 215355865 | 215441068 |
g0115 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FN1_chr2_215355865_215441068 | FN1 | chr2 | 215355865 | 215441068 |
g0116 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FN1_chr2_215355865_215441068 | FN1 | chr2 | 215355865 | 215441068 |
g0117 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FN1_chr2_215355865_215441068 | FN1 | chr2 | 215355865 | 215441068 |
g0118 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FN1_chr2_215355865_215441068 | FN1 | chr2 | 215355865 | 215441068 |
g0119 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FN1_chr2_215355865_215441068 | FN1 | chr2 | 215355865 | 215441068 |
g0120 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FN1_chr2_215355865_215441068 | FN1 | chr2 | 215355865 | 215441068 |
g0121 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FN1_chr2_215355865_215441068 | FN1 | chr2 | 215355865 | 215441068 |
g0122 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | FN1_chr2_215355865_215441068 | FN1 | chr2 | 215355865 | 215441068 |
g0123 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FN1_chr2_215355865_215441068 | FN1 | chr2 | 215355865 | 215441068 |
g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FN1_chr2_215355865_215441068 | FN1 | chr2 | 215355865 | 215441068 |
g0125 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FN1_chr2_215355865_215441068 | FN1 | chr2 | 215355865 | 215441068 |
g0126 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FN1_chr2_215355865_215441068 | FN1 | chr2 | 215355865 | 215441068 |
g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FN1_chr2_215355865_215441068 | FN1 | chr2 | 215355865 | 215441068 |
g0128 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FN1_chr2_215355865_215441068 | FN1 | chr2 | 215355865 | 215441068 |
g0129 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FN1_chr2_215355865_215441068 | FN1 | chr2 | 215355865 | 215441068 |
g0130 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FN1_chr2_215355865_215441068 | FN1 | chr2 | 215355865 | 215441068 |
g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FN1_chr2_215355865_215441068 | FN1 | chr2 | 215355865 | 215441068 |
g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FN1_chr2_215355865_215441068 | FN1 | chr2 | 215355865 | 215441068 |
g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FN1_chr2_215355865_215441068 | FN1 | chr2 | 215355865 | 215441068 |
g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FN1_chr2_215355865_215441068 | FN1 | chr2 | 215355865 | 215441068 |
g0135 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FN1_chr2_215355865_215441068 | FN1 | chr2 | 215355865 | 215441068 |
g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FN1_chr2_215355865_215441068 | FN1 | chr2 | 215355865 | 215441068 |
g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FN1_chr2_215355865_215441068 | FN1 | chr2 | 215355865 | 215441068 |
g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FN1_chr2_215355865_215441068 | FN1 | chr2 | 215355865 | 215441068 |
g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FN1_chr2_215355865_215441068 | FN1 | chr2 | 215355865 | 215441068 |
g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FN1_chr2_215355865_215441068 | FN1 | chr2 | 215355865 | 215441068 |
g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FN1_chr2_215355865_215441068 | FN1 | chr2 | 215355865 | 215441068 |
g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FN1_chr2_215355865_215441068 | FN1 | chr2 | 215355865 | 215441068 |
g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FN1_chr2_215355865_215441068 | FN1 | chr2 | 215355865 | 215441068 |
g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FN1_chr2_215355865_215441068 | FN1 | chr2 | 215355865 | 215441068 |
g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FN1_chr2_215355865_215441068 | FN1 | chr2 | 215355865 | 215441068 |
g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FN1_chr2_215355865_215441068 | FN1 | chr2 | 215355865 | 215441068 |
g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FN1_chr2_215355865_215441068 | FN1 | chr2 | 215355865 | 215441068 |
g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FN1_chr2_215355865_215441068 | FN1 | chr2 | 215355865 | 215441068 |
g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FN1_chr2_215355865_215441068 | FN1 | chr2 | 215355865 | 215441068 |
g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FN1_chr2_215355865_215441068 | FN1 | chr2 | 215355865 | 215441068 |
g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FN1_chr2_215355865_215441068 | FN1 | chr2 | 215355865 | 215441068 |
g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FN1_chr2_215355865_215441068 | FN1 | chr2 | 215355865 | 215441068 |
g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FN1_chr2_215355865_215441068 | FN1 | chr2 | 215355865 | 215441068 |
g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FN1_chr2_215355865_215441068 | FN1 | chr2 | 215355865 | 215441068 |
g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FN1_chr2_215355865_215441068 | FN1 | chr2 | 215355865 | 215441068 |
g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FN1_chr2_215355865_215441068 | FN1 | chr2 | 215355865 | 215441068 |
g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FN1_chr2_215355865_215441068 | FN1 | chr2 | 215355865 | 215441068 |
g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FN1_chr2_215355865_215441068 | FN1 | chr2 | 215355865 | 215441068 |
g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FN1_chr2_215355865_215441068 | FN1 | chr2 | 215355865 | 215441068 |
g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FN1_chr2_215355865_215441068 | FN1 | chr2 | 215355865 | 215441068 |
g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FN1_chr2_215355865_215441068 | FN1 | chr2 | 215355865 | 215441068 |
g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FN1_chr2_215355865_215441068 | FN1 | chr2 | 215355865 | 215441068 |
g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FN1_chr2_215355865_215441068 | FN1 | chr2 | 215355865 | 215441068 |
g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FN1_chr2_215355865_215441068 | FN1 | chr2 | 215355865 | 215441068 |
g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FN1_chr2_215355865_215441068 | FN1 | chr2 | 215355865 | 215441068 |
g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FN1_chr2_215355865_215441068 | FN1 | chr2 | 215355865 | 215441068 |
g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FN1_chr2_215355865_215441068 | FN1 | chr2 | 215355865 | 215441068 |
g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FN1_chr2_215355865_215441068 | FN1 | chr2 | 215355865 | 215441068 |
g0169 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FN1_chr2_215355865_215441068 | FN1 | chr2 | 215355865 | 215441068 |
g0170 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FN1_chr2_215355865_215441068 | FN1 | chr2 | 215355865 | 215441068 |
g0171 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FN1_chr2_215355865_215441068 | FN1 | chr2 | 215355865 | 215441068 |
g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FN1_chr2_215355865_215441068 | FN1 | chr2 | 215355865 | 215441068 |
g0173 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FN1_chr2_215355865_215441068 | FN1 | chr2 | 215355865 | 215441068 |
g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FN1_chr2_215355865_215441068 | FN1 | chr2 | 215355865 | 215441068 |
g0175 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FN1_chr2_215355865_215441068 | FN1 | chr2 | 215355865 | 215441068 |
g0176 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FN1_chr2_215355865_215441068 | FN1 | chr2 | 215355865 | 215441068 |
g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FN1_chr2_215355865_215441068 | FN1 | chr2 | 215355865 | 215441068 |
g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FN1_chr2_215355865_215441068 | FN1 | chr2 | 215355865 | 215441068 |
g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FN1_chr2_215355865_215441068 | FN1 | chr2 | 215355865 | 215441068 |
g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FN1_chr2_215355865_215441068 | FN1 | chr2 | 215355865 | 215441068 |
g0181 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FN1_chr2_215355865_215441068 | FN1 | chr2 | 215355865 | 215441068 |
g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FN1_chr2_215355865_215441068 | FN1 | chr2 | 215355865 | 215441068 |
g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FN1_chr2_215355865_215441068 | FN1 | chr2 | 215355865 | 215441068 |
g0184 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FN1_chr2_215355865_215441068 | FN1 | chr2 | 215355865 | 215441068 |
g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FN1_chr2_215355865_215441068 | FN1 | chr2 | 215355865 | 215441068 |
g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FN1_chr2_215355865_215441068 | FN1 | chr2 | 215355865 | 215441068 |
g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FN1_chr2_215355865_215441068 | FN1 | chr2 | 215355865 | 215441068 |
g0188 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FN1_chr2_215355865_215441068 | FN1 | chr2 | 215355865 | 215441068 |
g0189 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FN1_chr2_215355865_215441068 | FN1 | chr2 | 215355865 | 215441068 |
g0190 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FN1_chr2_215355865_215441068 | FN1 | chr2 | 215355865 | 215441068 |
g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FN1_chr2_215355865_215441068 | FN1 | chr2 | 215355865 | 215441068 |
g0192 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FN1_chr2_215355865_215441068 | FN1 | chr2 | 215355865 | 215441068 |
g0193 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FN1_chr2_215355865_215441068 | FN1 | chr2 | 215355865 | 215441068 |
g0194 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FN1_chr2_215355865_215441068 | FN1 | chr2 | 215355865 | 215441068 |
g0195 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FN1_chr2_215355865_215441068 | FN1 | chr2 | 215355865 | 215441068 |
g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FN1_chr2_215355865_215441068 | FN1 | chr2 | 215355865 | 215441068 |
g0197 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FN1_chr2_215355865_215441068 | FN1 | chr2 | 215355865 | 215441068 |
g0198 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FN1_chr2_215355865_215441068 | FN1 | chr2 | 215355865 | 215441068 |
g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FN1_chr2_215355865_215441068 | FN1 | chr2 | 215355865 | 215441068 |
g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FN1_chr2_215355865_215441068 | FN1 | chr2 | 215355865 | 215441068 |
g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FN1_chr2_215355865_215441068 | FN1 | chr2 | 215355865 | 215441068 |
g0202 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FN1_chr2_215355865_215441068 | FN1 | chr2 | 215355865 | 215441068 |
g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FN1_chr2_215355865_215441068 | FN1 | chr2 | 215355865 | 215441068 |
g0204 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FN1_chr2_215355865_215441068 | FN1 | chr2 | 215355865 | 215441068 |
g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FN1_chr2_215355865_215441068 | FN1 | chr2 | 215355865 | 215441068 |
g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FN1_chr2_215355865_215441068 | FN1 | chr2 | 215355865 | 215441068 |
g0207 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FN1_chr2_215355865_215441068 | FN1 | chr2 | 215355865 | 215441068 |
g0208 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FN1_chr2_215355865_215441068 | FN1 | chr2 | 215355865 | 215441068 |
g0209 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FN1_chr2_215355865_215441068 | FN1 | chr2 | 215355865 | 215441068 |
g0210 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FN1_chr2_215355865_215441068 | FN1 | chr2 | 215355865 | 215441068 |
g0211 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FN1_chr2_215355865_215441068 | FN1 | chr2 | 215355865 | 215441068 |
g0212 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FN1_chr2_215355865_215441068 | FN1 | chr2 | 215355865 | 215441068 |
g0213 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FN1_chr2_215355865_215441068 | FN1 | chr2 | 215355865 | 215441068 |
g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FN1_chr2_215355865_215441068 | FN1 | chr2 | 215355865 | 215441068 |
g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FN1_chr2_215355865_215441068 | FN1 | chr2 | 215355865 | 215441068 |
g0216 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FN1_chr2_215355865_215441068 | FN1 | chr2 | 215355865 | 215441068 |
g0217 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FN1_chr2_215355865_215441068 | FN1 | chr2 | 215355865 | 215441068 |
g0218 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FN1_chr2_215355865_215441068 | FN1 | chr2 | 215355865 | 215441068 |
g0219 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FN1_chr2_215355865_215441068 | FN1 | chr2 | 215355865 | 215441068 |
g0220 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FN1_chr2_215355865_215441068 | FN1 | chr2 | 215355865 | 215441068 |
g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FN1_chr2_215355865_215441068 | FN1 | chr2 | 215355865 | 215441068 |
g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FN1_chr2_215355865_215441068 | FN1 | chr2 | 215355865 | 215441068 |
g0223 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FN1_chr2_215355865_215441068 | FN1 | chr2 | 215355865 | 215441068 |
g0224 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FN1_chr2_215355865_215441068 | FN1 | chr2 | 215355865 | 215441068 |
g0225 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FN1_chr2_215355865_215441068 | FN1 | chr2 | 215355865 | 215441068 |
g0226 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FN1_chr2_215355865_215441068 | FN1 | chr2 | 215355865 | 215441068 |
g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FN1_chr2_215355865_215441068 | FN1 | chr2 | 215355865 | 215441068 |
g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FN1_chr2_215355865_215441068 | FN1 | chr2 | 215355865 | 215441068 |
g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FN1_chr2_215355865_215441068 | FN1 | chr2 | 215355865 | 215441068 |
g0230 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FN1_chr2_215355865_215441068 | FN1 | chr2 | 215355865 | 215441068 |
g0231 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FN1_chr2_215355865_215441068 | FN1 | chr2 | 215355865 | 215441068 |
g0232 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FN1_chr2_215355865_215441068 | FN1 | chr2 | 215355865 | 215441068 |
g0233 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FN1_chr2_215355865_215441068 | FN1 | chr2 | 215355865 | 215441068 |
g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FN1_chr2_215355865_215441068 | FN1 | chr2 | 215355865 | 215441068 |
g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FN1_chr2_215355865_215441068 | FN1 | chr2 | 215355865 | 215441068 |
g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FN1_chr2_215355865_215441068 | FN1 | chr2 | 215355865 | 215441068 |
g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FN1_chr2_215355865_215441068 | FN1 | chr2 | 215355865 | 215441068 |
g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FN1_chr2_215355865_215441068 | FN1 | chr2 | 215355865 | 215441068 |
achapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 0/0 | 7434 | 39 | 2 | 15 | 14 | 2 | 6 | FN1_chr2_215355865_215441068 | FN1 | copy fasta | chr2 | 215355865 | 215441068 |
a0001c0002 | 0/1 | 7434 | 28 | 15 | 7 | 0 | 2 | 3 | FN1_chr2_215355865_215441068 | FN1 | copy fasta | chr2 | 215355865 | 215441068 |
a0001c0004 | 0/0 | 7434 | 13 | 2 | 6 | 0 | 0 | 5 | FN1_chr2_215355865_215441068 | FN1 | copy fasta | chr2 | 215355865 | 215441068 |
a0001c0005 | 0/0 | 7434 | 12 | 7 | 3 | 1 | 0 | 1 | FN1_chr2_215355865_215441068 | FN1 | copy fasta | chr2 | 215355865 | 215441068 |
a0001c0006 | 0/0 | 7434 | 12 | 8 | 3 | 0 | 1 | 0 | FN1_chr2_215355865_215441068 | FN1 | copy fasta | chr2 | 215355865 | 215441068 |
a0001c0009 | 0/0 | 7434 | 6 | 6 | 0 | 0 | 0 | 0 | FN1_chr2_215355865_215441068 | FN1 | copy fasta | chr2 | 215355865 | 215441068 |
a0001c0010 | 0/0 | 7434 | 5 | 0 | 2 | 3 | 0 | 0 | FN1_chr2_215355865_215441068 | FN1 | copy fasta | chr2 | 215355865 | 215441068 |
a0001c0011 | 0/0 | 7434 | 5 | 0 | 3 | 0 | 1 | 1 | FN1_chr2_215355865_215441068 | FN1 | copy fasta | chr2 | 215355865 | 215441068 |
a0001c0012 | 0/0 | 7434 | 5 | 1 | 1 | 0 | 2 | 1 | FN1_chr2_215355865_215441068 | FN1 | copy fasta | chr2 | 215355865 | 215441068 |
a0001c0015 | 0/0 | 7434 | 4 | 4 | 0 | 0 | 0 | 0 | FN1_chr2_215355865_215441068 | FN1 | copy fasta | chr2 | 215355865 | 215441068 |
a0001c0025 | 0/0 | 7434 | 2 | 2 | 0 | 0 | 0 | 0 | FN1_chr2_215355865_215441068 | FN1 | copy fasta | chr2 | 215355865 | 215441068 |
a0001c0027 | 0/0 | 7434 | 2 | 0 | 1 | 0 | 1 | 0 | FN1_chr2_215355865_215441068 | FN1 | copy fasta | chr2 | 215355865 | 215441068 |
a0001c0041 | 0/0 | 7434 | 1 | 1 | 0 | 0 | 0 | 0 | FN1_chr2_215355865_215441068 | FN1 | copy fasta | chr2 | 215355865 | 215441068 |
a0001c0042 | 0/0 | 7434 | 1 | 1 | 0 | 0 | 0 | 0 | FN1_chr2_215355865_215441068 | FN1 | copy fasta | chr2 | 215355865 | 215441068 |
a0001c0044 | 0/0 | 7434 | 1 | 1 | 0 | 0 | 0 | 0 | FN1_chr2_215355865_215441068 | FN1 | copy fasta | chr2 | 215355865 | 215441068 |
a0001c0045 | 0/0 | 7434 | 1 | 1 | 0 | 0 | 0 | 0 | FN1_chr2_215355865_215441068 | FN1 | copy fasta | chr2 | 215355865 | 215441068 |
a0001c0046 | 0/0 | 7434 | 1 | 1 | 0 | 0 | 0 | 0 | FN1_chr2_215355865_215441068 | FN1 | copy fasta | chr2 | 215355865 | 215441068 |
a0001c0050 | 0/0 | 7434 | 1 | 0 | 0 | 1 | 0 | 0 | FN1_chr2_215355865_215441068 | FN1 | copy fasta | chr2 | 215355865 | 215441068 |
a0001c0051 | 0/0 | 7434 | 1 | 0 | 0 | 0 | 1 | 0 | FN1_chr2_215355865_215441068 | FN1 | copy fasta | chr2 | 215355865 | 215441068 |
a0001c0052 | 0/0 | 7434 | 1 | 0 | 0 | 0 | 0 | 1 | FN1_chr2_215355865_215441068 | FN1 | copy fasta | chr2 | 215355865 | 215441068 |
a0001c0054 | 0/0 | 7434 | 1 | 0 | 0 | 1 | 0 | 0 | FN1_chr2_215355865_215441068 | FN1 | copy fasta | chr2 | 215355865 | 215441068 |
a0001c0055 | 0/0 | 7434 | 1 | 1 | 0 | 0 | 0 | 0 | FN1_chr2_215355865_215441068 | FN1 | copy fasta | chr2 | 215355865 | 215441068 |
a0001c0057 | 0/0 | 7434 | 1 | 0 | 0 | 0 | 0 | 1 | FN1_chr2_215355865_215441068 | FN1 | copy fasta | chr2 | 215355865 | 215441068 |
a0001c0058 | 0/0 | 7434 | 1 | 1 | 0 | 0 | 0 | 0 | FN1_chr2_215355865_215441068 | FN1 | copy fasta | chr2 | 215355865 | 215441068 |
a0001c0059 | 0/0 | 7434 | 1 | 0 | 1 | 0 | 0 | 0 | FN1_chr2_215355865_215441068 | FN1 | copy fasta | chr2 | 215355865 | 215441068 |
a0001c0060 | 0/0 | 7434 | 1 | 1 | 0 | 0 | 0 | 0 | FN1_chr2_215355865_215441068 | FN1 | copy fasta | chr2 | 215355865 | 215441068 |
a0001c0062 | 0/0 | 7434 | 1 | 1 | 0 | 0 | 0 | 0 | FN1_chr2_215355865_215441068 | FN1 | copy fasta | chr2 | 215355865 | 215441068 |
a0001c0063 | 0/0 | 7434 | 1 | 0 | 1 | 0 | 0 | 0 | FN1_chr2_215355865_215441068 | FN1 | copy fasta | chr2 | 215355865 | 215441068 |
a0001c0064 | 0/0 | 7434 | 1 | 0 | 1 | 0 | 0 | 0 | FN1_chr2_215355865_215441068 | FN1 | copy fasta | chr2 | 215355865 | 215441068 |
a0002c0003 | 0/0 | 7434 | 19 | 0 | 6 | 5 | 1 | 7 | FN1_chr2_215355865_215441068 | FN1 | copy fasta | chr2 | 215355865 | 215441068 |
a0002c0008 | 0/0 | 7434 | 8 | 0 | 4 | 2 | 1 | 1 | FN1_chr2_215355865_215441068 | FN1 | copy fasta | chr2 | 215355865 | 215441068 |
a0002c0013 | 0/0 | 7434 | 4 | 1 | 2 | 1 | 0 | 0 | FN1_chr2_215355865_215441068 | FN1 | copy fasta | chr2 | 215355865 | 215441068 |
a0002c0014 | 0/0 | 7434 | 4 | 3 | 1 | 0 | 0 | 0 | FN1_chr2_215355865_215441068 | FN1 | copy fasta | chr2 | 215355865 | 215441068 |
a0002c0021 | 0/0 | 7434 | 2 | 0 | 1 | 0 | 1 | 0 | FN1_chr2_215355865_215441068 | FN1 | copy fasta | chr2 | 215355865 | 215441068 |
a0002c0022 | 0/0 | 7434 | 2 | 0 | 1 | 0 | 0 | 1 | FN1_chr2_215355865_215441068 | FN1 | copy fasta | chr2 | 215355865 | 215441068 |
a0002c0023 | 0/0 | 7434 | 2 | 2 | 0 | 0 | 0 | 0 | FN1_chr2_215355865_215441068 | FN1 | copy fasta | chr2 | 215355865 | 215441068 |
a0002c0030 | 0/0 | 7434 | 1 | 0 | 0 | 0 | 1 | 0 | FN1_chr2_215355865_215441068 | FN1 | copy fasta | chr2 | 215355865 | 215441068 |
a0002c0031 | 0/0 | 7434 | 1 | 0 | 1 | 0 | 0 | 0 | FN1_chr2_215355865_215441068 | FN1 | copy fasta | chr2 | 215355865 | 215441068 |
a0002c0032 | 0/0 | 7434 | 1 | 0 | 0 | 1 | 0 | 0 | FN1_chr2_215355865_215441068 | FN1 | copy fasta | chr2 | 215355865 | 215441068 |
a0002c0033 | 0/0 | 7434 | 1 | 0 | 0 | 0 | 0 | 1 | FN1_chr2_215355865_215441068 | FN1 | copy fasta | chr2 | 215355865 | 215441068 |
a0002c0034 | 0/0 | 7434 | 1 | 0 | 0 | 0 | 0 | 1 | FN1_chr2_215355865_215441068 | FN1 | copy fasta | chr2 | 215355865 | 215441068 |
a0002c0037 | 0/0 | 7434 | 1 | 1 | 0 | 0 | 0 | 0 | FN1_chr2_215355865_215441068 | FN1 | copy fasta | chr2 | 215355865 | 215441068 |
a0003c0007 | 0/0 | 7434 | 9 | 9 | 0 | 0 | 0 | 0 | FN1_chr2_215355865_215441068 | FN1 | copy fasta | chr2 | 215355865 | 215441068 |
a0003c0048 | 0/0 | 7434 | 1 | 1 | 0 | 0 | 0 | 0 | FN1_chr2_215355865_215441068 | FN1 | copy fasta | chr2 | 215355865 | 215441068 |
a0003c0056 | 0/0 | 7434 | 1 | 1 | 0 | 0 | 0 | 0 | FN1_chr2_215355865_215441068 | FN1 | copy fasta | chr2 | 215355865 | 215441068 |
a0004c0019 | 0/0 | 7434 | 2 | 2 | 0 | 0 | 0 | 0 | FN1_chr2_215355865_215441068 | FN1 | copy fasta | chr2 | 215355865 | 215441068 |
a0004c0020 | 0/0 | 7434 | 2 | 2 | 0 | 0 | 0 | 0 | FN1_chr2_215355865_215441068 | FN1 | copy fasta | chr2 | 215355865 | 215441068 |
a0005c0029 | 0/0 | 7434 | 2 | 2 | 0 | 0 | 0 | 0 | FN1_chr2_215355865_215441068 | FN1 | copy fasta | chr2 | 215355865 | 215441068 |
a0005c0065 | 0/0 | 7434 | 1 | 1 | 0 | 0 | 0 | 0 | FN1_chr2_215355865_215441068 | FN1 | copy fasta | chr2 | 215355865 | 215441068 |
a0006c0024 | 0/0 | 7434 | 2 | 2 | 0 | 0 | 0 | 0 | FN1_chr2_215355865_215441068 | FN1 | copy fasta | chr2 | 215355865 | 215441068 |
a0006c0040 | 0/0 | 7434 | 1 | 1 | 0 | 0 | 0 | 0 | FN1_chr2_215355865_215441068 | FN1 | copy fasta | chr2 | 215355865 | 215441068 |
a0007c0017 | 0/0 | 7434 | 3 | 2 | 1 | 0 | 0 | 0 | FN1_chr2_215355865_215441068 | FN1 | copy fasta | chr2 | 215355865 | 215441068 |
a0008c0018 | 0/0 | 7434 | 3 | 0 | 2 | 0 | 0 | 1 | FN1_chr2_215355865_215441068 | FN1 | copy fasta | chr2 | 215355865 | 215441068 |
a0009c0016 | 0/0 | 7434 | 3 | 0 | 3 | 0 | 0 | 0 | FN1_chr2_215355865_215441068 | FN1 | copy fasta | chr2 | 215355865 | 215441068 |
a0010c0028 | 0/0 | 7434 | 2 | 2 | 0 | 0 | 0 | 0 | FN1_chr2_215355865_215441068 | FN1 | copy fasta | chr2 | 215355865 | 215441068 |
a0011c0026 | 0/0 | 7434 | 2 | 2 | 0 | 0 | 0 | 0 | FN1_chr2_215355865_215441068 | FN1 | copy fasta | chr2 | 215355865 | 215441068 |
a0012c0047 | 0/0 | 7434 | 1 | 0 | 0 | 1 | 0 | 0 | FN1_chr2_215355865_215441068 | FN1 | copy fasta | chr2 | 215355865 | 215441068 |
a0013c0061 | 0/0 | 7434 | 1 | 1 | 0 | 0 | 0 | 0 | FN1_chr2_215355865_215441068 | FN1 | copy fasta | chr2 | 215355865 | 215441068 |
a0014c0049 | 0/0 | 7434 | 1 | 0 | 0 | 0 | 0 | 1 | FN1_chr2_215355865_215441068 | FN1 | copy fasta | chr2 | 215355865 | 215441068 |
a0015c0053 | 0/0 | 7434 | 1 | 0 | 0 | 1 | 0 | 0 | FN1_chr2_215355865_215441068 | FN1 | copy fasta | chr2 | 215355865 | 215441068 |
a0016c0043 | 0/0 | 7434 | 1 | 0 | 0 | 1 | 0 | 0 | FN1_chr2_215355865_215441068 | FN1 | copy fasta | chr2 | 215355865 | 215441068 |
a0017c0039 | 0/0 | 7434 | 1 | 0 | 0 | 0 | 0 | 1 | FN1_chr2_215355865_215441068 | FN1 | copy fasta | chr2 | 215355865 | 215441068 |
a0018c0038 | 0/0 | 7434 | 1 | 1 | 0 | 0 | 0 | 0 | FN1_chr2_215355865_215441068 | FN1 | copy fasta | chr2 | 215355865 | 215441068 |
a0019c0036 | 0/0 | 7434 | 1 | 0 | 0 | 0 | 0 | 1 | FN1_chr2_215355865_215441068 | FN1 | copy fasta | chr2 | 215355865 | 215441068 |
a0020c0035 | 1/0 | 7434 | 1 | 0 | 0 | 0 | 0 | 0 | FN1_chr2_215355865_215441068 | FN1 | copy fasta | chr2 | 215355865 | 215441068 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 0/0 | 8390 | 39 | 2 | 15 | 14 | 2 | 6 | FN1_chr2_215355865_215441068 | FN1 | copy fasta | chr2 | 215355865 | 215441068 |
a0001c0002t0001 | 0/1 | 8390 | 28 | 15 | 7 | 0 | 2 | 3 | FN1_chr2_215355865_215441068 | FN1 | copy fasta | chr2 | 215355865 | 215441068 |
a0001c0004t0001 | 0/0 | 8390 | 13 | 2 | 6 | 0 | 0 | 5 | FN1_chr2_215355865_215441068 | FN1 | copy fasta | chr2 | 215355865 | 215441068 |
a0001c0005t0001 | 0/0 | 8390 | 12 | 7 | 3 | 1 | 0 | 1 | FN1_chr2_215355865_215441068 | FN1 | copy fasta | chr2 | 215355865 | 215441068 |
a0001c0006t0001 | 0/0 | 8390 | 7 | 3 | 3 | 0 | 1 | 0 | FN1_chr2_215355865_215441068 | FN1 | copy fasta | chr2 | 215355865 | 215441068 |
a0001c0006t0002 | 0/0 | 8390 | 1 | 1 | 0 | 0 | 0 | 0 | FN1_chr2_215355865_215441068 | FN1 | copy fasta | chr2 | 215355865 | 215441068 |
a0001c0006t0003 | 0/0 | 8390 | 3 | 3 | 0 | 0 | 0 | 0 | FN1_chr2_215355865_215441068 | FN1 | copy fasta | chr2 | 215355865 | 215441068 |
a0001c0006t0004 | 0/0 | 8390 | 1 | 1 | 0 | 0 | 0 | 0 | FN1_chr2_215355865_215441068 | FN1 | copy fasta | chr2 | 215355865 | 215441068 |
a0001c0009t0001 | 0/0 | 8390 | 4 | 4 | 0 | 0 | 0 | 0 | FN1_chr2_215355865_215441068 | FN1 | copy fasta | chr2 | 215355865 | 215441068 |
a0001c0009t0002 | 0/0 | 8390 | 1 | 1 | 0 | 0 | 0 | 0 | FN1_chr2_215355865_215441068 | FN1 | copy fasta | chr2 | 215355865 | 215441068 |
a0001c0009t0003 | 0/0 | 8390 | 1 | 1 | 0 | 0 | 0 | 0 | FN1_chr2_215355865_215441068 | FN1 | copy fasta | chr2 | 215355865 | 215441068 |
a0001c0010t0001 | 0/0 | 8390 | 5 | 0 | 2 | 3 | 0 | 0 | FN1_chr2_215355865_215441068 | FN1 | copy fasta | chr2 | 215355865 | 215441068 |
a0001c0011t0001 | 0/0 | 8390 | 5 | 0 | 3 | 0 | 1 | 1 | FN1_chr2_215355865_215441068 | FN1 | copy fasta | chr2 | 215355865 | 215441068 |
a0001c0012t0001 | 0/0 | 8390 | 5 | 1 | 1 | 0 | 2 | 1 | FN1_chr2_215355865_215441068 | FN1 | copy fasta | chr2 | 215355865 | 215441068 |
a0001c0015t0001 | 0/0 | 8390 | 4 | 4 | 0 | 0 | 0 | 0 | FN1_chr2_215355865_215441068 | FN1 | copy fasta | chr2 | 215355865 | 215441068 |
a0001c0025t0001 | 0/0 | 8390 | 2 | 2 | 0 | 0 | 0 | 0 | FN1_chr2_215355865_215441068 | FN1 | copy fasta | chr2 | 215355865 | 215441068 |
a0001c0027t0001 | 0/0 | 8390 | 2 | 0 | 1 | 0 | 1 | 0 | FN1_chr2_215355865_215441068 | FN1 | copy fasta | chr2 | 215355865 | 215441068 |
a0001c0041t0001 | 0/0 | 8390 | 1 | 1 | 0 | 0 | 0 | 0 | FN1_chr2_215355865_215441068 | FN1 | copy fasta | chr2 | 215355865 | 215441068 |
a0001c0042t0001 | 0/0 | 8390 | 1 | 1 | 0 | 0 | 0 | 0 | FN1_chr2_215355865_215441068 | FN1 | copy fasta | chr2 | 215355865 | 215441068 |
a0001c0044t0001 | 0/0 | 8390 | 1 | 1 | 0 | 0 | 0 | 0 | FN1_chr2_215355865_215441068 | FN1 | copy fasta | chr2 | 215355865 | 215441068 |
a0001c0045t0001 | 0/0 | 8390 | 1 | 1 | 0 | 0 | 0 | 0 | FN1_chr2_215355865_215441068 | FN1 | copy fasta | chr2 | 215355865 | 215441068 |
a0001c0046t0001 | 0/0 | 8390 | 1 | 1 | 0 | 0 | 0 | 0 | FN1_chr2_215355865_215441068 | FN1 | copy fasta | chr2 | 215355865 | 215441068 |
a0001c0050t0001 | 0/0 | 8390 | 1 | 0 | 0 | 1 | 0 | 0 | FN1_chr2_215355865_215441068 | FN1 | copy fasta | chr2 | 215355865 | 215441068 |
a0001c0051t0001 | 0/0 | 8390 | 1 | 0 | 0 | 0 | 1 | 0 | FN1_chr2_215355865_215441068 | FN1 | copy fasta | chr2 | 215355865 | 215441068 |
a0001c0052t0001 | 0/0 | 8390 | 1 | 0 | 0 | 0 | 0 | 1 | FN1_chr2_215355865_215441068 | FN1 | copy fasta | chr2 | 215355865 | 215441068 |
a0001c0054t0001 | 0/0 | 8390 | 1 | 0 | 0 | 1 | 0 | 0 | FN1_chr2_215355865_215441068 | FN1 | copy fasta | chr2 | 215355865 | 215441068 |
a0001c0055t0001 | 0/0 | 8390 | 1 | 1 | 0 | 0 | 0 | 0 | FN1_chr2_215355865_215441068 | FN1 | copy fasta | chr2 | 215355865 | 215441068 |
a0001c0057t0001 | 0/0 | 8390 | 1 | 0 | 0 | 0 | 0 | 1 | FN1_chr2_215355865_215441068 | FN1 | copy fasta | chr2 | 215355865 | 215441068 |
a0001c0058t0002 | 0/0 | 8390 | 1 | 1 | 0 | 0 | 0 | 0 | FN1_chr2_215355865_215441068 | FN1 | copy fasta | chr2 | 215355865 | 215441068 |
a0001c0059t0001 | 0/0 | 8390 | 1 | 0 | 1 | 0 | 0 | 0 | FN1_chr2_215355865_215441068 | FN1 | copy fasta | chr2 | 215355865 | 215441068 |
a0001c0060t0001 | 0/0 | 8390 | 1 | 1 | 0 | 0 | 0 | 0 | FN1_chr2_215355865_215441068 | FN1 | copy fasta | chr2 | 215355865 | 215441068 |
a0001c0062t0003 | 0/0 | 8390 | 1 | 1 | 0 | 0 | 0 | 0 | FN1_chr2_215355865_215441068 | FN1 | copy fasta | chr2 | 215355865 | 215441068 |
a0001c0063t0001 | 0/0 | 8390 | 1 | 0 | 1 | 0 | 0 | 0 | FN1_chr2_215355865_215441068 | FN1 | copy fasta | chr2 | 215355865 | 215441068 |
a0001c0064t0001 | 0/0 | 8390 | 1 | 0 | 1 | 0 | 0 | 0 | FN1_chr2_215355865_215441068 | FN1 | copy fasta | chr2 | 215355865 | 215441068 |
a0002c0003t0001 | 0/0 | 8390 | 19 | 0 | 6 | 5 | 1 | 7 | FN1_chr2_215355865_215441068 | FN1 | copy fasta | chr2 | 215355865 | 215441068 |
a0002c0008t0001 | 0/0 | 8390 | 8 | 0 | 4 | 2 | 1 | 1 | FN1_chr2_215355865_215441068 | FN1 | copy fasta | chr2 | 215355865 | 215441068 |
a0002c0013t0001 | 0/0 | 8390 | 4 | 1 | 2 | 1 | 0 | 0 | FN1_chr2_215355865_215441068 | FN1 | copy fasta | chr2 | 215355865 | 215441068 |
a0002c0014t0001 | 0/0 | 8390 | 4 | 3 | 1 | 0 | 0 | 0 | FN1_chr2_215355865_215441068 | FN1 | copy fasta | chr2 | 215355865 | 215441068 |
a0002c0021t0001 | 0/0 | 8390 | 2 | 0 | 1 | 0 | 1 | 0 | FN1_chr2_215355865_215441068 | FN1 | copy fasta | chr2 | 215355865 | 215441068 |
a0002c0022t0001 | 0/0 | 8390 | 2 | 0 | 1 | 0 | 0 | 1 | FN1_chr2_215355865_215441068 | FN1 | copy fasta | chr2 | 215355865 | 215441068 |
a0002c0023t0001 | 0/0 | 8390 | 2 | 2 | 0 | 0 | 0 | 0 | FN1_chr2_215355865_215441068 | FN1 | copy fasta | chr2 | 215355865 | 215441068 |
a0002c0030t0001 | 0/0 | 8390 | 1 | 0 | 0 | 0 | 1 | 0 | FN1_chr2_215355865_215441068 | FN1 | copy fasta | chr2 | 215355865 | 215441068 |
a0002c0031t0001 | 0/0 | 8390 | 1 | 0 | 1 | 0 | 0 | 0 | FN1_chr2_215355865_215441068 | FN1 | copy fasta | chr2 | 215355865 | 215441068 |
a0002c0032t0001 | 0/0 | 8390 | 1 | 0 | 0 | 1 | 0 | 0 | FN1_chr2_215355865_215441068 | FN1 | copy fasta | chr2 | 215355865 | 215441068 |
a0002c0033t0001 | 0/0 | 8390 | 1 | 0 | 0 | 0 | 0 | 1 | FN1_chr2_215355865_215441068 | FN1 | copy fasta | chr2 | 215355865 | 215441068 |
a0002c0034t0001 | 0/0 | 8390 | 1 | 0 | 0 | 0 | 0 | 1 | FN1_chr2_215355865_215441068 | FN1 | copy fasta | chr2 | 215355865 | 215441068 |
a0002c0037t0001 | 0/0 | 8390 | 1 | 1 | 0 | 0 | 0 | 0 | FN1_chr2_215355865_215441068 | FN1 | copy fasta | chr2 | 215355865 | 215441068 |
a0003c0007t0001 | 0/0 | 8390 | 2 | 2 | 0 | 0 | 0 | 0 | FN1_chr2_215355865_215441068 | FN1 | copy fasta | chr2 | 215355865 | 215441068 |
a0003c0007t0002 | 0/0 | 8390 | 7 | 7 | 0 | 0 | 0 | 0 | FN1_chr2_215355865_215441068 | FN1 | copy fasta | chr2 | 215355865 | 215441068 |
a0003c0048t0002 | 0/0 | 8390 | 1 | 1 | 0 | 0 | 0 | 0 | FN1_chr2_215355865_215441068 | FN1 | copy fasta | chr2 | 215355865 | 215441068 |
a0003c0056t0002 | 0/0 | 8390 | 1 | 1 | 0 | 0 | 0 | 0 | FN1_chr2_215355865_215441068 | FN1 | copy fasta | chr2 | 215355865 | 215441068 |
a0004c0019t0001 | 0/0 | 8390 | 2 | 2 | 0 | 0 | 0 | 0 | FN1_chr2_215355865_215441068 | FN1 | copy fasta | chr2 | 215355865 | 215441068 |
a0004c0020t0002 | 0/0 | 8390 | 2 | 2 | 0 | 0 | 0 | 0 | FN1_chr2_215355865_215441068 | FN1 | copy fasta | chr2 | 215355865 | 215441068 |
a0005c0029t0003 | 0/0 | 8390 | 2 | 2 | 0 | 0 | 0 | 0 | FN1_chr2_215355865_215441068 | FN1 | copy fasta | chr2 | 215355865 | 215441068 |
a0005c0065t0001 | 0/0 | 8390 | 1 | 1 | 0 | 0 | 0 | 0 | FN1_chr2_215355865_215441068 | FN1 | copy fasta | chr2 | 215355865 | 215441068 |
a0006c0024t0001 | 0/0 | 8390 | 2 | 2 | 0 | 0 | 0 | 0 | FN1_chr2_215355865_215441068 | FN1 | copy fasta | chr2 | 215355865 | 215441068 |
a0006c0040t0001 | 0/0 | 8390 | 1 | 1 | 0 | 0 | 0 | 0 | FN1_chr2_215355865_215441068 | FN1 | copy fasta | chr2 | 215355865 | 215441068 |
a0007c0017t0001 | 0/0 | 8390 | 3 | 2 | 1 | 0 | 0 | 0 | FN1_chr2_215355865_215441068 | FN1 | copy fasta | chr2 | 215355865 | 215441068 |
a0008c0018t0001 | 0/0 | 8390 | 3 | 0 | 2 | 0 | 0 | 1 | FN1_chr2_215355865_215441068 | FN1 | copy fasta | chr2 | 215355865 | 215441068 |
a0009c0016t0001 | 0/0 | 8390 | 3 | 0 | 3 | 0 | 0 | 0 | FN1_chr2_215355865_215441068 | FN1 | copy fasta | chr2 | 215355865 | 215441068 |
a0010c0028t0002 | 0/0 | 8390 | 2 | 2 | 0 | 0 | 0 | 0 | FN1_chr2_215355865_215441068 | FN1 | copy fasta | chr2 | 215355865 | 215441068 |
a0011c0026t0001 | 0/0 | 8390 | 2 | 2 | 0 | 0 | 0 | 0 | FN1_chr2_215355865_215441068 | FN1 | copy fasta | chr2 | 215355865 | 215441068 |
a0012c0047t0001 | 0/0 | 8390 | 1 | 0 | 0 | 1 | 0 | 0 | FN1_chr2_215355865_215441068 | FN1 | copy fasta | chr2 | 215355865 | 215441068 |
a0013c0061t0001 | 0/0 | 8390 | 1 | 1 | 0 | 0 | 0 | 0 | FN1_chr2_215355865_215441068 | FN1 | copy fasta | chr2 | 215355865 | 215441068 |
a0014c0049t0001 | 0/0 | 8390 | 1 | 0 | 0 | 0 | 0 | 1 | FN1_chr2_215355865_215441068 | FN1 | copy fasta | chr2 | 215355865 | 215441068 |
a0015c0053t0001 | 0/0 | 8390 | 1 | 0 | 0 | 1 | 0 | 0 | FN1_chr2_215355865_215441068 | FN1 | copy fasta | chr2 | 215355865 | 215441068 |
a0016c0043t0001 | 0/0 | 8390 | 1 | 0 | 0 | 1 | 0 | 0 | FN1_chr2_215355865_215441068 | FN1 | copy fasta | chr2 | 215355865 | 215441068 |
a0017c0039t0001 | 0/0 | 8390 | 1 | 0 | 0 | 0 | 0 | 1 | FN1_chr2_215355865_215441068 | FN1 | copy fasta | chr2 | 215355865 | 215441068 |
a0018c0038t0002 | 0/0 | 8390 | 1 | 1 | 0 | 0 | 0 | 0 | FN1_chr2_215355865_215441068 | FN1 | copy fasta | chr2 | 215355865 | 215441068 |
a0019c0036t0001 | 0/0 | 8390 | 1 | 0 | 0 | 0 | 0 | 1 | FN1_chr2_215355865_215441068 | FN1 | copy fasta | chr2 | 215355865 | 215441068 |
a0020c0035t0001 | 1/0 | 8390 | 1 | 0 | 0 | 0 | 0 | 0 | FN1_chr2_215355865_215441068 | FN1 | copy fasta | chr2 | 215355865 | 215441068 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0002 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | FN1_chr2_215355865_215441068 | FN1 | chr2 | 215355865 | 215441068 |
a0001c0001t0001g0062 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FN1_chr2_215355865_215441068 | FN1 | chr2 | 215355865 | 215441068 |
a0001c0001t0001g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FN1_chr2_215355865_215441068 | FN1 | chr2 | 215355865 | 215441068 |
a0001c0001t0001g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FN1_chr2_215355865_215441068 | FN1 | chr2 | 215355865 | 215441068 |
a0001c0001t0001g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FN1_chr2_215355865_215441068 | FN1 | chr2 | 215355865 | 215441068 |
a0001c0001t0001g0169 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FN1_chr2_215355865_215441068 | FN1 | chr2 | 215355865 | 215441068 |
a0001c0001t0001g0171 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FN1_chr2_215355865_215441068 | FN1 | chr2 | 215355865 | 215441068 |
a0001c0001t0001g0173 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FN1_chr2_215355865_215441068 | FN1 | chr2 | 215355865 | 215441068 |
a0001c0001t0001g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FN1_chr2_215355865_215441068 | FN1 | chr2 | 215355865 | 215441068 |
a0001c0001t0001g0175 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FN1_chr2_215355865_215441068 | FN1 | chr2 | 215355865 | 215441068 |
a0001c0001t0001g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FN1_chr2_215355865_215441068 | FN1 | chr2 | 215355865 | 215441068 |
a0001c0001t0001g0181 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FN1_chr2_215355865_215441068 | FN1 | chr2 | 215355865 | 215441068 |
a0001c0001t0001g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FN1_chr2_215355865_215441068 | FN1 | chr2 | 215355865 | 215441068 |
a0001c0001t0001g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FN1_chr2_215355865_215441068 | FN1 | chr2 | 215355865 | 215441068 |
a0001c0001t0001g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FN1_chr2_215355865_215441068 | FN1 | chr2 | 215355865 | 215441068 |
a0001c0001t0001g0188 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FN1_chr2_215355865_215441068 | FN1 | chr2 | 215355865 | 215441068 |
a0001c0001t0001g0189 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FN1_chr2_215355865_215441068 | FN1 | chr2 | 215355865 | 215441068 |
a0001c0001t0001g0192 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FN1_chr2_215355865_215441068 | FN1 | chr2 | 215355865 | 215441068 |
a0001c0001t0001g0193 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FN1_chr2_215355865_215441068 | FN1 | chr2 | 215355865 | 215441068 |
a0001c0001t0001g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FN1_chr2_215355865_215441068 | FN1 | chr2 | 215355865 | 215441068 |
a0001c0001t0001g0197 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FN1_chr2_215355865_215441068 | FN1 | chr2 | 215355865 | 215441068 |
a0001c0001t0001g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FN1_chr2_215355865_215441068 | FN1 | chr2 | 215355865 | 215441068 |
a0001c0001t0001g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FN1_chr2_215355865_215441068 | FN1 | chr2 | 215355865 | 215441068 |
a0001c0001t0001g0202 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FN1_chr2_215355865_215441068 | FN1 | chr2 | 215355865 | 215441068 |
a0001c0001t0001g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FN1_chr2_215355865_215441068 | FN1 | chr2 | 215355865 | 215441068 |
a0001c0001t0001g0204 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FN1_chr2_215355865_215441068 | FN1 | chr2 | 215355865 | 215441068 |
a0001c0001t0001g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FN1_chr2_215355865_215441068 | FN1 | chr2 | 215355865 | 215441068 |
a0001c0001t0001g0208 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FN1_chr2_215355865_215441068 | FN1 | chr2 | 215355865 | 215441068 |
a0001c0001t0001g0209 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FN1_chr2_215355865_215441068 | FN1 | chr2 | 215355865 | 215441068 |
a0001c0001t0001g0210 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FN1_chr2_215355865_215441068 | FN1 | chr2 | 215355865 | 215441068 |
a0001c0001t0001g0211 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FN1_chr2_215355865_215441068 | FN1 | chr2 | 215355865 | 215441068 |
a0001c0001t0001g0212 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FN1_chr2_215355865_215441068 | FN1 | chr2 | 215355865 | 215441068 |
a0001c0001t0001g0213 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FN1_chr2_215355865_215441068 | FN1 | chr2 | 215355865 | 215441068 |
a0001c0001t0001g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FN1_chr2_215355865_215441068 | FN1 | chr2 | 215355865 | 215441068 |
a0001c0001t0001g0216 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FN1_chr2_215355865_215441068 | FN1 | chr2 | 215355865 | 215441068 |
a0001c0001t0001g0217 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FN1_chr2_215355865_215441068 | FN1 | chr2 | 215355865 | 215441068 |
a0001c0001t0001g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FN1_chr2_215355865_215441068 | FN1 | chr2 | 215355865 | 215441068 |
a0001c0001t0001g0226 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FN1_chr2_215355865_215441068 | FN1 | chr2 | 215355865 | 215441068 |
a0001c0002t0001g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FN1_chr2_215355865_215441068 | FN1 | chr2 | 215355865 | 215441068 |
a0001c0002t0001g0112 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FN1_chr2_215355865_215441068 | FN1 | chr2 | 215355865 | 215441068 |
a0001c0002t0001g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FN1_chr2_215355865_215441068 | FN1 | chr2 | 215355865 | 215441068 |
a0001c0002t0001g0114 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FN1_chr2_215355865_215441068 | FN1 | chr2 | 215355865 | 215441068 |
a0001c0002t0001g0119 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FN1_chr2_215355865_215441068 | FN1 | chr2 | 215355865 | 215441068 |
a0001c0002t0001g0121 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FN1_chr2_215355865_215441068 | FN1 | chr2 | 215355865 | 215441068 |
a0001c0002t0001g0122 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | FN1_chr2_215355865_215441068 | FN1 | chr2 | 215355865 | 215441068 |
a0001c0002t0001g0123 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FN1_chr2_215355865_215441068 | FN1 | chr2 | 215355865 | 215441068 |
a0001c0002t0001g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FN1_chr2_215355865_215441068 | FN1 | chr2 | 215355865 | 215441068 |
a0001c0002t0001g0126 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FN1_chr2_215355865_215441068 | FN1 | chr2 | 215355865 | 215441068 |
a0001c0002t0001g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FN1_chr2_215355865_215441068 | FN1 | chr2 | 215355865 | 215441068 |
a0001c0002t0001g0128 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FN1_chr2_215355865_215441068 | FN1 | chr2 | 215355865 | 215441068 |
a0001c0002t0001g0129 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FN1_chr2_215355865_215441068 | FN1 | chr2 | 215355865 | 215441068 |
a0001c0002t0001g0130 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FN1_chr2_215355865_215441068 | FN1 | chr2 | 215355865 | 215441068 |
a0001c0002t0001g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FN1_chr2_215355865_215441068 | FN1 | chr2 | 215355865 | 215441068 |
a0001c0002t0001g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FN1_chr2_215355865_215441068 | FN1 | chr2 | 215355865 | 215441068 |
a0001c0002t0001g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FN1_chr2_215355865_215441068 | FN1 | chr2 | 215355865 | 215441068 |
a0001c0002t0001g0135 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FN1_chr2_215355865_215441068 | FN1 | chr2 | 215355865 | 215441068 |
a0001c0002t0001g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FN1_chr2_215355865_215441068 | FN1 | chr2 | 215355865 | 215441068 |
a0001c0002t0001g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FN1_chr2_215355865_215441068 | FN1 | chr2 | 215355865 | 215441068 |
a0001c0002t0001g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FN1_chr2_215355865_215441068 | FN1 | chr2 | 215355865 | 215441068 |
a0001c0002t0001g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FN1_chr2_215355865_215441068 | FN1 | chr2 | 215355865 | 215441068 |
a0001c0002t0001g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FN1_chr2_215355865_215441068 | FN1 | chr2 | 215355865 | 215441068 |
a0001c0002t0001g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FN1_chr2_215355865_215441068 | FN1 | chr2 | 215355865 | 215441068 |
a0001c0002t0001g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FN1_chr2_215355865_215441068 | FN1 | chr2 | 215355865 | 215441068 |
a0001c0002t0001g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FN1_chr2_215355865_215441068 | FN1 | chr2 | 215355865 | 215441068 |
a0001c0002t0001g0232 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FN1_chr2_215355865_215441068 | FN1 | chr2 | 215355865 | 215441068 |
a0001c0002t0001g0233 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FN1_chr2_215355865_215441068 | FN1 | chr2 | 215355865 | 215441068 |
a0001c0004t0001g0001 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | FN1_chr2_215355865_215441068 | FN1 | chr2 | 215355865 | 215441068 |
a0001c0004t0001g0068 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FN1_chr2_215355865_215441068 | FN1 | chr2 | 215355865 | 215441068 |
a0001c0004t0001g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FN1_chr2_215355865_215441068 | FN1 | chr2 | 215355865 | 215441068 |
a0001c0004t0001g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FN1_chr2_215355865_215441068 | FN1 | chr2 | 215355865 | 215441068 |
a0001c0004t0001g0080 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FN1_chr2_215355865_215441068 | FN1 | chr2 | 215355865 | 215441068 |
a0001c0004t0001g0082 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FN1_chr2_215355865_215441068 | FN1 | chr2 | 215355865 | 215441068 |
a0001c0004t0001g0083 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FN1_chr2_215355865_215441068 | FN1 | chr2 | 215355865 | 215441068 |
a0001c0004t0001g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FN1_chr2_215355865_215441068 | FN1 | chr2 | 215355865 | 215441068 |
a0001c0004t0001g0085 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FN1_chr2_215355865_215441068 | FN1 | chr2 | 215355865 | 215441068 |
a0001c0004t0001g0086 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FN1_chr2_215355865_215441068 | FN1 | chr2 | 215355865 | 215441068 |
a0001c0004t0001g0087 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FN1_chr2_215355865_215441068 | FN1 | chr2 | 215355865 | 215441068 |
a0001c0004t0001g0231 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FN1_chr2_215355865_215441068 | FN1 | chr2 | 215355865 | 215441068 |
a0001c0005t0001g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FN1_chr2_215355865_215441068 | FN1 | chr2 | 215355865 | 215441068 |
a0001c0005t0001g0176 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FN1_chr2_215355865_215441068 | FN1 | chr2 | 215355865 | 215441068 |
a0001c0005t0001g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FN1_chr2_215355865_215441068 | FN1 | chr2 | 215355865 | 215441068 |
a0001c0005t0001g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FN1_chr2_215355865_215441068 | FN1 | chr2 | 215355865 | 215441068 |
a0001c0005t0001g0190 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FN1_chr2_215355865_215441068 | FN1 | chr2 | 215355865 | 215441068 |
a0001c0005t0001g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FN1_chr2_215355865_215441068 | FN1 | chr2 | 215355865 | 215441068 |
a0001c0005t0001g0198 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FN1_chr2_215355865_215441068 | FN1 | chr2 | 215355865 | 215441068 |
a0001c0005t0001g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FN1_chr2_215355865_215441068 | FN1 | chr2 | 215355865 | 215441068 |
a0001c0005t0001g0218 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FN1_chr2_215355865_215441068 | FN1 | chr2 | 215355865 | 215441068 |
a0001c0005t0001g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FN1_chr2_215355865_215441068 | FN1 | chr2 | 215355865 | 215441068 |
a0001c0005t0001g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FN1_chr2_215355865_215441068 | FN1 | chr2 | 215355865 | 215441068 |
a0001c0005t0001g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FN1_chr2_215355865_215441068 | FN1 | chr2 | 215355865 | 215441068 |
a0001c0006t0001g0069 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FN1_chr2_215355865_215441068 | FN1 | chr2 | 215355865 | 215441068 |
a0001c0006t0001g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FN1_chr2_215355865_215441068 | FN1 | chr2 | 215355865 | 215441068 |
a0001c0006t0001g0075 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FN1_chr2_215355865_215441068 | FN1 | chr2 | 215355865 | 215441068 |
a0001c0006t0001g0090 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FN1_chr2_215355865_215441068 | FN1 | chr2 | 215355865 | 215441068 |
a0001c0006t0001g0091 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FN1_chr2_215355865_215441068 | FN1 | chr2 | 215355865 | 215441068 |
a0001c0006t0001g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FN1_chr2_215355865_215441068 | FN1 | chr2 | 215355865 | 215441068 |
a0001c0006t0001g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FN1_chr2_215355865_215441068 | FN1 | chr2 | 215355865 | 215441068 |
a0001c0006t0002g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FN1_chr2_215355865_215441068 | FN1 | chr2 | 215355865 | 215441068 |
a0001c0006t0003g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FN1_chr2_215355865_215441068 | FN1 | chr2 | 215355865 | 215441068 |
a0001c0006t0003g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FN1_chr2_215355865_215441068 | FN1 | chr2 | 215355865 | 215441068 |
a0001c0006t0003g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FN1_chr2_215355865_215441068 | FN1 | chr2 | 215355865 | 215441068 |
a0001c0006t0004g0003 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FN1_chr2_215355865_215441068 | FN1 | chr2 | 215355865 | 215441068 |
a0001c0009t0001g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FN1_chr2_215355865_215441068 | FN1 | chr2 | 215355865 | 215441068 |
a0001c0009t0001g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FN1_chr2_215355865_215441068 | FN1 | chr2 | 215355865 | 215441068 |
a0001c0009t0001g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FN1_chr2_215355865_215441068 | FN1 | chr2 | 215355865 | 215441068 |
a0001c0009t0001g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FN1_chr2_215355865_215441068 | FN1 | chr2 | 215355865 | 215441068 |
a0001c0009t0002g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FN1_chr2_215355865_215441068 | FN1 | chr2 | 215355865 | 215441068 |
a0001c0009t0003g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FN1_chr2_215355865_215441068 | FN1 | chr2 | 215355865 | 215441068 |
a0001c0010t0001g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FN1_chr2_215355865_215441068 | FN1 | chr2 | 215355865 | 215441068 |
a0001c0010t0001g0184 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FN1_chr2_215355865_215441068 | FN1 | chr2 | 215355865 | 215441068 |
a0001c0010t0001g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FN1_chr2_215355865_215441068 | FN1 | chr2 | 215355865 | 215441068 |
a0001c0010t0001g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FN1_chr2_215355865_215441068 | FN1 | chr2 | 215355865 | 215441068 |
a0001c0010t0001g0230 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FN1_chr2_215355865_215441068 | FN1 | chr2 | 215355865 | 215441068 |
a0001c0011t0001g0106 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FN1_chr2_215355865_215441068 | FN1 | chr2 | 215355865 | 215441068 |
a0001c0011t0001g0107 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FN1_chr2_215355865_215441068 | FN1 | chr2 | 215355865 | 215441068 |
a0001c0011t0001g0108 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FN1_chr2_215355865_215441068 | FN1 | chr2 | 215355865 | 215441068 |
a0001c0011t0001g0109 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FN1_chr2_215355865_215441068 | FN1 | chr2 | 215355865 | 215441068 |
a0001c0011t0001g0220 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FN1_chr2_215355865_215441068 | FN1 | chr2 | 215355865 | 215441068 |
a0001c0012t0001g0079 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FN1_chr2_215355865_215441068 | FN1 | chr2 | 215355865 | 215441068 |
a0001c0012t0001g0081 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FN1_chr2_215355865_215441068 | FN1 | chr2 | 215355865 | 215441068 |
a0001c0012t0001g0089 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FN1_chr2_215355865_215441068 | FN1 | chr2 | 215355865 | 215441068 |
a0001c0012t0001g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FN1_chr2_215355865_215441068 | FN1 | chr2 | 215355865 | 215441068 |
a0001c0012t0001g0170 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FN1_chr2_215355865_215441068 | FN1 | chr2 | 215355865 | 215441068 |
a0001c0015t0001g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FN1_chr2_215355865_215441068 | FN1 | chr2 | 215355865 | 215441068 |
a0001c0015t0001g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FN1_chr2_215355865_215441068 | FN1 | chr2 | 215355865 | 215441068 |
a0001c0015t0001g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FN1_chr2_215355865_215441068 | FN1 | chr2 | 215355865 | 215441068 |
a0001c0015t0001g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FN1_chr2_215355865_215441068 | FN1 | chr2 | 215355865 | 215441068 |
a0001c0025t0001g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FN1_chr2_215355865_215441068 | FN1 | chr2 | 215355865 | 215441068 |
a0001c0025t0001g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FN1_chr2_215355865_215441068 | FN1 | chr2 | 215355865 | 215441068 |
a0001c0027t0001g0063 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FN1_chr2_215355865_215441068 | FN1 | chr2 | 215355865 | 215441068 |
a0001c0027t0001g0120 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FN1_chr2_215355865_215441068 | FN1 | chr2 | 215355865 | 215441068 |
a0001c0041t0001g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FN1_chr2_215355865_215441068 | FN1 | chr2 | 215355865 | 215441068 |
a0001c0042t0001g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FN1_chr2_215355865_215441068 | FN1 | chr2 | 215355865 | 215441068 |
a0001c0044t0001g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FN1_chr2_215355865_215441068 | FN1 | chr2 | 215355865 | 215441068 |
a0001c0045t0001g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FN1_chr2_215355865_215441068 | FN1 | chr2 | 215355865 | 215441068 |
a0001c0046t0001g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FN1_chr2_215355865_215441068 | FN1 | chr2 | 215355865 | 215441068 |
a0001c0050t0001g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FN1_chr2_215355865_215441068 | FN1 | chr2 | 215355865 | 215441068 |
a0001c0051t0001g0207 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FN1_chr2_215355865_215441068 | FN1 | chr2 | 215355865 | 215441068 |
a0001c0052t0001g0195 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FN1_chr2_215355865_215441068 | FN1 | chr2 | 215355865 | 215441068 |
a0001c0054t0001g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FN1_chr2_215355865_215441068 | FN1 | chr2 | 215355865 | 215441068 |
a0001c0055t0001g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FN1_chr2_215355865_215441068 | FN1 | chr2 | 215355865 | 215441068 |
a0001c0057t0001g0105 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FN1_chr2_215355865_215441068 | FN1 | chr2 | 215355865 | 215441068 |
a0001c0058t0002g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FN1_chr2_215355865_215441068 | FN1 | chr2 | 215355865 | 215441068 |
a0001c0059t0001g0219 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FN1_chr2_215355865_215441068 | FN1 | chr2 | 215355865 | 215441068 |
a0001c0060t0001g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FN1_chr2_215355865_215441068 | FN1 | chr2 | 215355865 | 215441068 |
a0001c0062t0003g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FN1_chr2_215355865_215441068 | FN1 | chr2 | 215355865 | 215441068 |
a0001c0063t0001g0125 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FN1_chr2_215355865_215441068 | FN1 | chr2 | 215355865 | 215441068 |
a0001c0064t0001g0117 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FN1_chr2_215355865_215441068 | FN1 | chr2 | 215355865 | 215441068 |
a0002c0003t0001g0013 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FN1_chr2_215355865_215441068 | FN1 | chr2 | 215355865 | 215441068 |
a0002c0003t0001g0016 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FN1_chr2_215355865_215441068 | FN1 | chr2 | 215355865 | 215441068 |
a0002c0003t0001g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FN1_chr2_215355865_215441068 | FN1 | chr2 | 215355865 | 215441068 |
a0002c0003t0001g0024 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FN1_chr2_215355865_215441068 | FN1 | chr2 | 215355865 | 215441068 |
a0002c0003t0001g0026 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FN1_chr2_215355865_215441068 | FN1 | chr2 | 215355865 | 215441068 |
a0002c0003t0001g0028 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FN1_chr2_215355865_215441068 | FN1 | chr2 | 215355865 | 215441068 |
a0002c0003t0001g0029 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FN1_chr2_215355865_215441068 | FN1 | chr2 | 215355865 | 215441068 |
a0002c0003t0001g0030 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FN1_chr2_215355865_215441068 | FN1 | chr2 | 215355865 | 215441068 |
a0002c0003t0001g0032 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FN1_chr2_215355865_215441068 | FN1 | chr2 | 215355865 | 215441068 |
a0002c0003t0001g0034 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FN1_chr2_215355865_215441068 | FN1 | chr2 | 215355865 | 215441068 |
a0002c0003t0001g0036 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FN1_chr2_215355865_215441068 | FN1 | chr2 | 215355865 | 215441068 |
a0002c0003t0001g0037 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FN1_chr2_215355865_215441068 | FN1 | chr2 | 215355865 | 215441068 |
a0002c0003t0001g0039 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FN1_chr2_215355865_215441068 | FN1 | chr2 | 215355865 | 215441068 |
a0002c0003t0001g0040 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FN1_chr2_215355865_215441068 | FN1 | chr2 | 215355865 | 215441068 |
a0002c0003t0001g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FN1_chr2_215355865_215441068 | FN1 | chr2 | 215355865 | 215441068 |
a0002c0003t0001g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FN1_chr2_215355865_215441068 | FN1 | chr2 | 215355865 | 215441068 |
a0002c0003t0001g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FN1_chr2_215355865_215441068 | FN1 | chr2 | 215355865 | 215441068 |
a0002c0003t0001g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FN1_chr2_215355865_215441068 | FN1 | chr2 | 215355865 | 215441068 |
a0002c0003t0001g0057 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FN1_chr2_215355865_215441068 | FN1 | chr2 | 215355865 | 215441068 |
a0002c0008t0001g0008 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FN1_chr2_215355865_215441068 | FN1 | chr2 | 215355865 | 215441068 |
a0002c0008t0001g0021 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FN1_chr2_215355865_215441068 | FN1 | chr2 | 215355865 | 215441068 |
a0002c0008t0001g0027 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FN1_chr2_215355865_215441068 | FN1 | chr2 | 215355865 | 215441068 |
a0002c0008t0001g0033 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FN1_chr2_215355865_215441068 | FN1 | chr2 | 215355865 | 215441068 |
a0002c0008t0001g0035 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FN1_chr2_215355865_215441068 | FN1 | chr2 | 215355865 | 215441068 |
a0002c0008t0001g0041 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FN1_chr2_215355865_215441068 | FN1 | chr2 | 215355865 | 215441068 |
a0002c0008t0001g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FN1_chr2_215355865_215441068 | FN1 | chr2 | 215355865 | 215441068 |
a0002c0008t0001g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FN1_chr2_215355865_215441068 | FN1 | chr2 | 215355865 | 215441068 |
a0002c0013t0001g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FN1_chr2_215355865_215441068 | FN1 | chr2 | 215355865 | 215441068 |
a0002c0013t0001g0010 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FN1_chr2_215355865_215441068 | FN1 | chr2 | 215355865 | 215441068 |
a0002c0013t0001g0011 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FN1_chr2_215355865_215441068 | FN1 | chr2 | 215355865 | 215441068 |
a0002c0013t0001g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FN1_chr2_215355865_215441068 | FN1 | chr2 | 215355865 | 215441068 |
a0002c0014t0001g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FN1_chr2_215355865_215441068 | FN1 | chr2 | 215355865 | 215441068 |
a0002c0014t0001g0053 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FN1_chr2_215355865_215441068 | FN1 | chr2 | 215355865 | 215441068 |
a0002c0014t0001g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FN1_chr2_215355865_215441068 | FN1 | chr2 | 215355865 | 215441068 |
a0002c0014t0001g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FN1_chr2_215355865_215441068 | FN1 | chr2 | 215355865 | 215441068 |
a0002c0021t0001g0023 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FN1_chr2_215355865_215441068 | FN1 | chr2 | 215355865 | 215441068 |
a0002c0021t0001g0025 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FN1_chr2_215355865_215441068 | FN1 | chr2 | 215355865 | 215441068 |
a0002c0022t0001g0014 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FN1_chr2_215355865_215441068 | FN1 | chr2 | 215355865 | 215441068 |
a0002c0022t0001g0015 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FN1_chr2_215355865_215441068 | FN1 | chr2 | 215355865 | 215441068 |
a0002c0023t0001g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FN1_chr2_215355865_215441068 | FN1 | chr2 | 215355865 | 215441068 |
a0002c0023t0001g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FN1_chr2_215355865_215441068 | FN1 | chr2 | 215355865 | 215441068 |
a0002c0030t0001g0017 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FN1_chr2_215355865_215441068 | FN1 | chr2 | 215355865 | 215441068 |
a0002c0031t0001g0048 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FN1_chr2_215355865_215441068 | FN1 | chr2 | 215355865 | 215441068 |
a0002c0032t0001g0012 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FN1_chr2_215355865_215441068 | FN1 | chr2 | 215355865 | 215441068 |
a0002c0033t0001g0018 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FN1_chr2_215355865_215441068 | FN1 | chr2 | 215355865 | 215441068 |
a0002c0034t0001g0055 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FN1_chr2_215355865_215441068 | FN1 | chr2 | 215355865 | 215441068 |
a0002c0037t0001g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FN1_chr2_215355865_215441068 | FN1 | chr2 | 215355865 | 215441068 |
a0003c0007t0001g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FN1_chr2_215355865_215441068 | FN1 | chr2 | 215355865 | 215441068 |
a0003c0007t0001g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FN1_chr2_215355865_215441068 | FN1 | chr2 | 215355865 | 215441068 |
a0003c0007t0002g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FN1_chr2_215355865_215441068 | FN1 | chr2 | 215355865 | 215441068 |
a0003c0007t0002g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FN1_chr2_215355865_215441068 | FN1 | chr2 | 215355865 | 215441068 |
a0003c0007t0002g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FN1_chr2_215355865_215441068 | FN1 | chr2 | 215355865 | 215441068 |
a0003c0007t0002g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FN1_chr2_215355865_215441068 | FN1 | chr2 | 215355865 | 215441068 |
a0003c0007t0002g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FN1_chr2_215355865_215441068 | FN1 | chr2 | 215355865 | 215441068 |
a0003c0007t0002g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FN1_chr2_215355865_215441068 | FN1 | chr2 | 215355865 | 215441068 |
a0003c0007t0002g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FN1_chr2_215355865_215441068 | FN1 | chr2 | 215355865 | 215441068 |
a0003c0048t0002g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FN1_chr2_215355865_215441068 | FN1 | chr2 | 215355865 | 215441068 |
a0003c0056t0002g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FN1_chr2_215355865_215441068 | FN1 | chr2 | 215355865 | 215441068 |
a0004c0019t0001g0004 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FN1_chr2_215355865_215441068 | FN1 | chr2 | 215355865 | 215441068 |
a0004c0019t0001g0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FN1_chr2_215355865_215441068 | FN1 | chr2 | 215355865 | 215441068 |
a0004c0020t0002g0005 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FN1_chr2_215355865_215441068 | FN1 | chr2 | 215355865 | 215441068 |
a0004c0020t0002g0006 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FN1_chr2_215355865_215441068 | FN1 | chr2 | 215355865 | 215441068 |
a0005c0029t0003g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FN1_chr2_215355865_215441068 | FN1 | chr2 | 215355865 | 215441068 |
a0005c0029t0003g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FN1_chr2_215355865_215441068 | FN1 | chr2 | 215355865 | 215441068 |
a0005c0065t0001g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FN1_chr2_215355865_215441068 | FN1 | chr2 | 215355865 | 215441068 |
a0006c0024t0001g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FN1_chr2_215355865_215441068 | FN1 | chr2 | 215355865 | 215441068 |
a0006c0024t0001g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FN1_chr2_215355865_215441068 | FN1 | chr2 | 215355865 | 215441068 |
a0006c0040t0001g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FN1_chr2_215355865_215441068 | FN1 | chr2 | 215355865 | 215441068 |
a0007c0017t0001g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FN1_chr2_215355865_215441068 | FN1 | chr2 | 215355865 | 215441068 |
a0007c0017t0001g0092 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FN1_chr2_215355865_215441068 | FN1 | chr2 | 215355865 | 215441068 |
a0007c0017t0001g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FN1_chr2_215355865_215441068 | FN1 | chr2 | 215355865 | 215441068 |
a0008c0018t0001g0115 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FN1_chr2_215355865_215441068 | FN1 | chr2 | 215355865 | 215441068 |
a0008c0018t0001g0116 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FN1_chr2_215355865_215441068 | FN1 | chr2 | 215355865 | 215441068 |
a0008c0018t0001g0118 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FN1_chr2_215355865_215441068 | FN1 | chr2 | 215355865 | 215441068 |
a0009c0016t0001g0223 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FN1_chr2_215355865_215441068 | FN1 | chr2 | 215355865 | 215441068 |
a0009c0016t0001g0224 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FN1_chr2_215355865_215441068 | FN1 | chr2 | 215355865 | 215441068 |
a0009c0016t0001g0225 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FN1_chr2_215355865_215441068 | FN1 | chr2 | 215355865 | 215441068 |
a0010c0028t0002g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FN1_chr2_215355865_215441068 | FN1 | chr2 | 215355865 | 215441068 |
a0010c0028t0002g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FN1_chr2_215355865_215441068 | FN1 | chr2 | 215355865 | 215441068 |
a0011c0026t0001g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FN1_chr2_215355865_215441068 | FN1 | chr2 | 215355865 | 215441068 |
a0011c0026t0001g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FN1_chr2_215355865_215441068 | FN1 | chr2 | 215355865 | 215441068 |
a0012c0047t0001g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FN1_chr2_215355865_215441068 | FN1 | chr2 | 215355865 | 215441068 |
a0013c0061t0001g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FN1_chr2_215355865_215441068 | FN1 | chr2 | 215355865 | 215441068 |
a0014c0049t0001g0194 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FN1_chr2_215355865_215441068 | FN1 | chr2 | 215355865 | 215441068 |
a0015c0053t0001g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FN1_chr2_215355865_215441068 | FN1 | chr2 | 215355865 | 215441068 |
a0016c0043t0001g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FN1_chr2_215355865_215441068 | FN1 | chr2 | 215355865 | 215441068 |
a0017c0039t0001g0031 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FN1_chr2_215355865_215441068 | FN1 | chr2 | 215355865 | 215441068 |
a0018c0038t0002g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FN1_chr2_215355865_215441068 | FN1 | chr2 | 215355865 | 215441068 |
a0019c0036t0001g0038 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FN1_chr2_215355865_215441068 | FN1 | chr2 | 215355865 | 215441068 |
a0020c0035t0001g0020 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | FN1_chr2_215355865_215441068 | FN1 | chr2 | 215355865 | 215441068 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0001 | c0012 | t0001 | g0079 | EUR | GBR | FN1_chr2_215355865_215441068 | FN1 | chr2 | 215355865 | 215441068 |
HG00099 | hp2 | a0001 | c0051 | t0001 | g0207 | EUR | GBR | FN1_chr2_215355865_215441068 | FN1 | chr2 | 215355865 | 215441068 |
HG00140 | hp1 | a0001 | c0006 | t0001 | g0075 | EUR | GBR | FN1_chr2_215355865_215441068 | FN1 | chr2 | 215355865 | 215441068 |
HG00140 | hp2 | a0001 | c0002 | t0001 | g0129 | EUR | GBR | FN1_chr2_215355865_215441068 | FN1 | chr2 | 215355865 | 215441068 |
HG00280 | hp1 | a0002 | c0030 | t0001 | g0017 | EUR | FIN | FN1_chr2_215355865_215441068 | FN1 | chr2 | 215355865 | 215441068 |
HG00280 | hp2 | a0001 | c0001 | t0001 | g0210 | EUR | FIN | FN1_chr2_215355865_215441068 | FN1 | chr2 | 215355865 | 215441068 |
HG00323 | hp1 | a0002 | c0008 | t0001 | g0008 | EUR | FIN | FN1_chr2_215355865_215441068 | FN1 | chr2 | 215355865 | 215441068 |
HG00323 | hp2 | a0001 | c0002 | t0001 | g0123 | EUR | FIN | FN1_chr2_215355865_215441068 | FN1 | chr2 | 215355865 | 215441068 |
HG00609 | hp1 | a0002 | c0032 | t0001 | g0012 | EAS | CHS | FN1_chr2_215355865_215441068 | FN1 | chr2 | 215355865 | 215441068 |
HG00609 | hp2 | a0001 | c0001 | t0001 | g0196 | EAS | CHS | FN1_chr2_215355865_215441068 | FN1 | chr2 | 215355865 | 215441068 |
HG00639 | hp1 | a0002 | c0003 | t0001 | g0024 | AMR | PUR | FN1_chr2_215355865_215441068 | FN1 | chr2 | 215355865 | 215441068 |
HG00639 | hp2 | a0001 | c0001 | t0001 | g0209 | AMR | PUR | FN1_chr2_215355865_215441068 | FN1 | chr2 | 215355865 | 215441068 |
HG00642 | hp1 | a0001 | c0005 | t0001 | g0198 | AMR | PUR | FN1_chr2_215355865_215441068 | FN1 | chr2 | 215355865 | 215441068 |
HG00642 | hp2 | a0001 | c0002 | t0001 | g0114 | AMR | PUR | FN1_chr2_215355865_215441068 | FN1 | chr2 | 215355865 | 215441068 |
HG00735 | hp1 | a0001 | c0001 | t0001 | g0216 | AMR | PUR | FN1_chr2_215355865_215441068 | FN1 | chr2 | 215355865 | 215441068 |
HG00735 | hp2 | a0001 | c0004 | t0001 | g0068 | AMR | PUR | FN1_chr2_215355865_215441068 | FN1 | chr2 | 215355865 | 215441068 |
HG00738 | hp1 | a0001 | c0002 | t0001 | g0126 | AMR | PUR | FN1_chr2_215355865_215441068 | FN1 | chr2 | 215355865 | 215441068 |
HG00738 | hp2 | a0001 | c0002 | t0001 | g0130 | AMR | PUR | FN1_chr2_215355865_215441068 | FN1 | chr2 | 215355865 | 215441068 |
HG00741 | hp1 | a0002 | c0021 | t0001 | g0023 | AMR | PUR | FN1_chr2_215355865_215441068 | FN1 | chr2 | 215355865 | 215441068 |
HG00741 | hp2 | a0002 | c0003 | t0001 | g0039 | AMR | PUR | FN1_chr2_215355865_215441068 | FN1 | chr2 | 215355865 | 215441068 |
HG01069 | hp1 | a0001 | c0001 | t0001 | g0208 | AMR | PUR | FN1_chr2_215355865_215441068 | FN1 | chr2 | 215355865 | 215441068 |
HG01069 | hp2 | a0001 | c0012 | t0001 | g0081 | AMR | PUR | FN1_chr2_215355865_215441068 | FN1 | chr2 | 215355865 | 215441068 |
HG01070 | hp1 | a0001 | c0001 | t0001 | g0213 | AMR | PUR | FN1_chr2_215355865_215441068 | FN1 | chr2 | 215355865 | 215441068 |
HG01070 | hp2 | a0002 | c0008 | t0001 | g0035 | AMR | PUR | FN1_chr2_215355865_215441068 | FN1 | chr2 | 215355865 | 215441068 |
HG01071 | hp1 | a0002 | c0008 | t0001 | g0033 | AMR | PUR | FN1_chr2_215355865_215441068 | FN1 | chr2 | 215355865 | 215441068 |
HG01071 | hp2 | a0001 | c0001 | t0001 | g0212 | AMR | PUR | FN1_chr2_215355865_215441068 | FN1 | chr2 | 215355865 | 215441068 |
HG01074 | hp1 | a0001 | c0001 | t0001 | g0202 | AMR | PUR | FN1_chr2_215355865_215441068 | FN1 | chr2 | 215355865 | 215441068 |
HG01074 | hp2 | a0002 | c0013 | t0001 | g0010 | AMR | PUR | FN1_chr2_215355865_215441068 | FN1 | chr2 | 215355865 | 215441068 |
HG01099 | hp1 | a0001 | c0006 | t0001 | g0069 | AMR | PUR | FN1_chr2_215355865_215441068 | FN1 | chr2 | 215355865 | 215441068 |
HG01099 | hp2 | a0001 | c0027 | t0001 | g0120 | AMR | PUR | FN1_chr2_215355865_215441068 | FN1 | chr2 | 215355865 | 215441068 |
HG01106 | hp1 | a0001 | c0004 | t0001 | g0001 | AMR | PUR | FN1_chr2_215355865_215441068 | FN1 | chr2 | 215355865 | 215441068 |
HG01106 | hp2 | a0001 | c0001 | t0001 | g0173 | AMR | PUR | FN1_chr2_215355865_215441068 | FN1 | chr2 | 215355865 | 215441068 |
HG01109 | hp1 | a0001 | c0063 | t0001 | g0125 | AMR | PUR | FN1_chr2_215355865_215441068 | FN1 | chr2 | 215355865 | 215441068 |
HG01109 | hp2 | a0001 | c0002 | t0001 | g0135 | AMR | PUR | FN1_chr2_215355865_215441068 | FN1 | chr2 | 215355865 | 215441068 |
HG01167 | hp1 | a0001 | c0001 | t0001 | g0192 | AMR | PUR | FN1_chr2_215355865_215441068 | FN1 | chr2 | 215355865 | 215441068 |
HG01167 | hp2 | a0002 | c0003 | t0001 | g0040 | AMR | PUR | FN1_chr2_215355865_215441068 | FN1 | chr2 | 215355865 | 215441068 |
HG01168 | hp1 | a0001 | c0011 | t0001 | g0109 | AMR | PUR | FN1_chr2_215355865_215441068 | FN1 | chr2 | 215355865 | 215441068 |
HG01168 | hp2 | a0001 | c0004 | t0001 | g0083 | AMR | PUR | FN1_chr2_215355865_215441068 | FN1 | chr2 | 215355865 | 215441068 |
HG01169 | hp1 | a0001 | c0004 | t0001 | g0084 | AMR | PUR | FN1_chr2_215355865_215441068 | FN1 | chr2 | 215355865 | 215441068 |
HG01169 | hp2 | a0001 | c0001 | t0001 | g0193 | AMR | PUR | FN1_chr2_215355865_215441068 | FN1 | chr2 | 215355865 | 215441068 |
HG01175 | hp1 | a0001 | c0002 | t0001 | g0121 | AMR | PUR | FN1_chr2_215355865_215441068 | FN1 | chr2 | 215355865 | 215441068 |
HG01175 | hp2 | a0002 | c0008 | t0001 | g0021 | AMR | PUR | FN1_chr2_215355865_215441068 | FN1 | chr2 | 215355865 | 215441068 |
HG01192 | hp1 | a0001 | c0001 | t0001 | g0197 | AMR | PUR | FN1_chr2_215355865_215441068 | FN1 | chr2 | 215355865 | 215441068 |
HG01192 | hp2 | a0001 | c0004 | t0001 | g0001 | AMR | PUR | FN1_chr2_215355865_215441068 | FN1 | chr2 | 215355865 | 215441068 |
HG01243 | hp1 | a0001 | c0002 | t0001 | g0112 | AMR | PUR | FN1_chr2_215355865_215441068 | FN1 | chr2 | 215355865 | 215441068 |
HG01243 | hp2 | a0001 | c0011 | t0001 | g0220 | AMR | PUR | FN1_chr2_215355865_215441068 | FN1 | chr2 | 215355865 | 215441068 |
HG01255 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | CLM | FN1_chr2_215355865_215441068 | FN1 | chr2 | 215355865 | 215441068 |
HG01255 | hp2 | a0008 | c0018 | t0001 | g0115 | AMR | CLM | FN1_chr2_215355865_215441068 | FN1 | chr2 | 215355865 | 215441068 |
HG01256 | hp1 | a0001 | c0004 | t0001 | g0080 | AMR | CLM | FN1_chr2_215355865_215441068 | FN1 | chr2 | 215355865 | 215441068 |
HG01256 | hp2 | a0001 | c0006 | t0001 | g0091 | AMR | CLM | FN1_chr2_215355865_215441068 | FN1 | chr2 | 215355865 | 215441068 |
HG01257 | hp1 | a0001 | c0002 | t0001 | g0119 | AMR | CLM | FN1_chr2_215355865_215441068 | FN1 | chr2 | 215355865 | 215441068 |
HG01257 | hp2 | a0009 | c0016 | t0001 | g0224 | AMR | CLM | FN1_chr2_215355865_215441068 | FN1 | chr2 | 215355865 | 215441068 |
HG01258 | hp1 | a0001 | c0006 | t0001 | g0090 | AMR | CLM | FN1_chr2_215355865_215441068 | FN1 | chr2 | 215355865 | 215441068 |
HG01258 | hp2 | a0009 | c0016 | t0001 | g0223 | AMR | CLM | FN1_chr2_215355865_215441068 | FN1 | chr2 | 215355865 | 215441068 |
HG01261 | hp1 | a0001 | c0064 | t0001 | g0117 | AMR | CLM | FN1_chr2_215355865_215441068 | FN1 | chr2 | 215355865 | 215441068 |
HG01261 | hp2 | a0002 | c0008 | t0001 | g0027 | AMR | CLM | FN1_chr2_215355865_215441068 | FN1 | chr2 | 215355865 | 215441068 |
HG01346 | hp1 | a0001 | c0011 | t0001 | g0107 | AMR | CLM | FN1_chr2_215355865_215441068 | FN1 | chr2 | 215355865 | 215441068 |
HG01346 | hp2 | a0001 | c0001 | t0001 | g0211 | AMR | CLM | FN1_chr2_215355865_215441068 | FN1 | chr2 | 215355865 | 215441068 |
HG01361 | hp1 | a0001 | c0010 | t0001 | g0230 | AMR | CLM | FN1_chr2_215355865_215441068 | FN1 | chr2 | 215355865 | 215441068 |
HG01361 | hp2 | a0008 | c0018 | t0001 | g0118 | AMR | CLM | FN1_chr2_215355865_215441068 | FN1 | chr2 | 215355865 | 215441068 |
HG01496 | hp1 | a0002 | c0031 | t0001 | g0048 | AMR | CLM | FN1_chr2_215355865_215441068 | FN1 | chr2 | 215355865 | 215441068 |
HG01496 | hp2 | a0002 | c0013 | t0001 | g0011 | AMR | CLM | FN1_chr2_215355865_215441068 | FN1 | chr2 | 215355865 | 215441068 |
HG01515 | hp1 | a0001 | c0001 | t0001 | g0062 | EUR | IBS | FN1_chr2_215355865_215441068 | FN1 | chr2 | 215355865 | 215441068 |
HG01515 | hp2 | a0001 | c0011 | t0001 | g0106 | EUR | IBS | FN1_chr2_215355865_215441068 | FN1 | chr2 | 215355865 | 215441068 |
HG01884 | hp1 | a0001 | c0002 | t0001 | g0138 | AFR | ACB | FN1_chr2_215355865_215441068 | FN1 | chr2 | 215355865 | 215441068 |
HG01884 | hp2 | a0002 | c0014 | t0001 | g0052 | AFR | ACB | FN1_chr2_215355865_215441068 | FN1 | chr2 | 215355865 | 215441068 |
HG01891 | hp1 | a0001 | c0002 | t0001 | g0127 | AFR | ACB | FN1_chr2_215355865_215441068 | FN1 | chr2 | 215355865 | 215441068 |
HG01891 | hp2 | a0002 | c0023 | t0001 | g0051 | AFR | ACB | FN1_chr2_215355865_215441068 | FN1 | chr2 | 215355865 | 215441068 |
HG01928 | hp1 | a0002 | c0003 | t0001 | g0028 | AMR | PEL | FN1_chr2_215355865_215441068 | FN1 | chr2 | 215355865 | 215441068 |
HG01928 | hp2 | a0001 | c0005 | t0001 | g0176 | AMR | PEL | FN1_chr2_215355865_215441068 | FN1 | chr2 | 215355865 | 215441068 |
HG01934 | hp1 | a0001 | c0010 | t0001 | g0184 | AMR | PEL | FN1_chr2_215355865_215441068 | FN1 | chr2 | 215355865 | 215441068 |
HG01934 | hp2 | a0002 | c0003 | t0001 | g0057 | AMR | PEL | FN1_chr2_215355865_215441068 | FN1 | chr2 | 215355865 | 215441068 |
HG01952 | hp1 | a0002 | c0022 | t0001 | g0014 | AMR | PEL | FN1_chr2_215355865_215441068 | FN1 | chr2 | 215355865 | 215441068 |
HG01952 | hp2 | a0009 | c0016 | t0001 | g0225 | AMR | PEL | FN1_chr2_215355865_215441068 | FN1 | chr2 | 215355865 | 215441068 |
HG01975 | hp1 | a0002 | c0014 | t0001 | g0053 | AMR | PEL | FN1_chr2_215355865_215441068 | FN1 | chr2 | 215355865 | 215441068 |
HG01975 | hp2 | a0001 | c0059 | t0001 | g0219 | AMR | PEL | FN1_chr2_215355865_215441068 | FN1 | chr2 | 215355865 | 215441068 |
HG01978 | hp1 | a0002 | c0003 | t0001 | g0032 | AMR | PEL | FN1_chr2_215355865_215441068 | FN1 | chr2 | 215355865 | 215441068 |
HG01978 | hp2 | a0001 | c0001 | t0001 | g0217 | AMR | PEL | FN1_chr2_215355865_215441068 | FN1 | chr2 | 215355865 | 215441068 |
HG02055 | hp1 | a0013 | c0061 | t0001 | g0143 | AFR | ACB | FN1_chr2_215355865_215441068 | FN1 | chr2 | 215355865 | 215441068 |
HG02055 | hp2 | a0001 | c0046 | t0001 | g0164 | AFR | ACB | FN1_chr2_215355865_215441068 | FN1 | chr2 | 215355865 | 215441068 |
HG02071 | hp1 | a0001 | c0001 | t0001 | g0199 | EAS | KHV | FN1_chr2_215355865_215441068 | FN1 | chr2 | 215355865 | 215441068 |
HG02071 | hp2 | a0002 | c0003 | t0001 | g0019 | EAS | KHV | FN1_chr2_215355865_215441068 | FN1 | chr2 | 215355865 | 215441068 |
HG02080 | hp1 | a0001 | c0050 | t0001 | g0182 | EAS | KHV | FN1_chr2_215355865_215441068 | FN1 | chr2 | 215355865 | 215441068 |
HG02080 | hp2 | a0001 | c0010 | t0001 | g0227 | EAS | KHV | FN1_chr2_215355865_215441068 | FN1 | chr2 | 215355865 | 215441068 |
HG02083 | hp1 | a0001 | c0001 | t0001 | g0203 | EAS | KHV | FN1_chr2_215355865_215441068 | FN1 | chr2 | 215355865 | 215441068 |
HG02083 | hp2 | a0002 | c0003 | t0001 | g0045 | EAS | KHV | FN1_chr2_215355865_215441068 | FN1 | chr2 | 215355865 | 215441068 |
HG02132 | hp1 | a0001 | c0001 | t0001 | g0174 | EAS | KHV | FN1_chr2_215355865_215441068 | FN1 | chr2 | 215355865 | 215441068 |
HG02132 | hp2 | a0001 | c0001 | t0001 | g0150 | EAS | KHV | FN1_chr2_215355865_215441068 | FN1 | chr2 | 215355865 | 215441068 |
HG02145 | hp1 | a0001 | c0002 | t0001 | g0134 | AFR | ACB | FN1_chr2_215355865_215441068 | FN1 | chr2 | 215355865 | 215441068 |
HG02145 | hp2 | a0001 | c0006 | t0003 | g0073 | AFR | ACB | FN1_chr2_215355865_215441068 | FN1 | chr2 | 215355865 | 215441068 |
HG02165 | hp1 | a0001 | c0001 | t0001 | g0187 | EAS | CDX | FN1_chr2_215355865_215441068 | FN1 | chr2 | 215355865 | 215441068 |
HG02165 | hp2 | a0001 | c0010 | t0001 | g0205 | EAS | CDX | FN1_chr2_215355865_215441068 | FN1 | chr2 | 215355865 | 215441068 |
HG02257 | hp1 | a0001 | c0005 | t0001 | g0178 | AFR | ACB | FN1_chr2_215355865_215441068 | FN1 | chr2 | 215355865 | 215441068 |
HG02257 | hp2 | a0018 | c0038 | t0002 | g0050 | AFR | ACB | FN1_chr2_215355865_215441068 | FN1 | chr2 | 215355865 | 215441068 |
HG02258 | hp1 | a0001 | c0025 | t0001 | g0162 | AFR | ACB | FN1_chr2_215355865_215441068 | FN1 | chr2 | 215355865 | 215441068 |
HG02258 | hp2 | a0001 | c0044 | t0001 | g0065 | AFR | ACB | FN1_chr2_215355865_215441068 | FN1 | chr2 | 215355865 | 215441068 |
HG02273 | hp1 | a0007 | c0017 | t0001 | g0092 | AMR | PEL | FN1_chr2_215355865_215441068 | FN1 | chr2 | 215355865 | 215441068 |
HG02273 | hp2 | a0001 | c0001 | t0001 | g0175 | AMR | PEL | FN1_chr2_215355865_215441068 | FN1 | chr2 | 215355865 | 215441068 |
HG02280 | hp1 | a0001 | c0002 | t0001 | g0111 | AFR | ACB | FN1_chr2_215355865_215441068 | FN1 | chr2 | 215355865 | 215441068 |
HG02280 | hp2 | a0001 | c0005 | t0001 | g0214 | AFR | ACB | FN1_chr2_215355865_215441068 | FN1 | chr2 | 215355865 | 215441068 |
HG02300 | hp1 | a0001 | c0001 | t0001 | g0226 | AMR | PEL | FN1_chr2_215355865_215441068 | FN1 | chr2 | 215355865 | 215441068 |
HG02300 | hp2 | a0001 | c0005 | t0001 | g0190 | AMR | PEL | FN1_chr2_215355865_215441068 | FN1 | chr2 | 215355865 | 215441068 |
HG02451 | hp1 | a0001 | c0004 | t0001 | g0070 | AFR | ACB | FN1_chr2_215355865_215441068 | FN1 | chr2 | 215355865 | 215441068 |
HG02451 | hp2 | a0001 | c0002 | t0001 | g0137 | AFR | ACB | FN1_chr2_215355865_215441068 | FN1 | chr2 | 215355865 | 215441068 |
HG02572 | hp1 | a0003 | c0048 | t0002 | g0100 | AFR | GWD | FN1_chr2_215355865_215441068 | FN1 | chr2 | 215355865 | 215441068 |
HG02572 | hp2 | a0001 | c0009 | t0001 | g0074 | AFR | GWD | FN1_chr2_215355865_215441068 | FN1 | chr2 | 215355865 | 215441068 |
HG02602 | hp1 | a0001 | c0001 | t0001 | g0181 | SAS | PJL | FN1_chr2_215355865_215441068 | FN1 | chr2 | 215355865 | 215441068 |
HG02602 | hp2 | a0001 | c0057 | t0001 | g0105 | SAS | PJL | FN1_chr2_215355865_215441068 | FN1 | chr2 | 215355865 | 215441068 |
HG02615 | hp1 | a0003 | c0007 | t0002 | g0093 | AFR | GWD | FN1_chr2_215355865_215441068 | FN1 | chr2 | 215355865 | 215441068 |
HG02615 | hp2 | a0001 | c0005 | t0001 | g0229 | AFR | GWD | FN1_chr2_215355865_215441068 | FN1 | chr2 | 215355865 | 215441068 |
HG02622 | hp1 | a0001 | c0001 | t0001 | g0177 | AFR | GWD | FN1_chr2_215355865_215441068 | FN1 | chr2 | 215355865 | 215441068 |
HG02622 | hp2 | a0001 | c0015 | t0001 | g0104 | AFR | GWD | FN1_chr2_215355865_215441068 | FN1 | chr2 | 215355865 | 215441068 |
HG02630 | hp1 | a0001 | c0009 | t0001 | g0155 | AFR | GWD | FN1_chr2_215355865_215441068 | FN1 | chr2 | 215355865 | 215441068 |
HG02630 | hp2 | a0001 | c0005 | t0001 | g0221 | AFR | GWD | FN1_chr2_215355865_215441068 | FN1 | chr2 | 215355865 | 215441068 |
HG02647 | hp1 | a0004 | c0019 | t0001 | g0007 | AFR | GWD | FN1_chr2_215355865_215441068 | FN1 | chr2 | 215355865 | 215441068 |
HG02647 | hp2 | a0001 | c0009 | t0001 | g0166 | AFR | GWD | FN1_chr2_215355865_215441068 | FN1 | chr2 | 215355865 | 215441068 |
HG02683 | hp1 | a0002 | c0003 | t0001 | g0037 | SAS | PJL | FN1_chr2_215355865_215441068 | FN1 | chr2 | 215355865 | 215441068 |
HG02683 | hp2 | a0002 | c0003 | t0001 | g0013 | SAS | PJL | FN1_chr2_215355865_215441068 | FN1 | chr2 | 215355865 | 215441068 |
HG02717 | hp1 | a0001 | c0009 | t0001 | g0157 | AFR | GWD | FN1_chr2_215355865_215441068 | FN1 | chr2 | 215355865 | 215441068 |
HG02717 | hp2 | a0001 | c0005 | t0001 | g0067 | AFR | GWD | FN1_chr2_215355865_215441068 | FN1 | chr2 | 215355865 | 215441068 |
HG02723 | hp1 | a0001 | c0025 | t0001 | g0163 | AFR | GWD | FN1_chr2_215355865_215441068 | FN1 | chr2 | 215355865 | 215441068 |
HG02723 | hp2 | a0001 | c0045 | t0001 | g0165 | AFR | GWD | FN1_chr2_215355865_215441068 | FN1 | chr2 | 215355865 | 215441068 |
HG02818 | hp1 | a0002 | c0014 | t0001 | g0056 | AFR | GWD | FN1_chr2_215355865_215441068 | FN1 | chr2 | 215355865 | 215441068 |
HG02818 | hp2 | a0001 | c0006 | t0001 | g0072 | AFR | GWD | FN1_chr2_215355865_215441068 | FN1 | chr2 | 215355865 | 215441068 |
HG02886 | hp1 | a0010 | c0028 | t0002 | g0237 | AFR | GWD | FN1_chr2_215355865_215441068 | FN1 | chr2 | 215355865 | 215441068 |
HG02886 | hp2 | a0003 | c0007 | t0001 | g0088 | AFR | GWD | FN1_chr2_215355865_215441068 | FN1 | chr2 | 215355865 | 215441068 |
HG02895 | hp1 | a0001 | c0002 | t0001 | g0113 | AFR | GWD | FN1_chr2_215355865_215441068 | FN1 | chr2 | 215355865 | 215441068 |
HG02895 | hp2 | a0001 | c0006 | t0003 | g0095 | AFR | GWD | FN1_chr2_215355865_215441068 | FN1 | chr2 | 215355865 | 215441068 |
HG02896 | hp1 | a0001 | c0006 | t0002 | g0077 | AFR | GWD | FN1_chr2_215355865_215441068 | FN1 | chr2 | 215355865 | 215441068 |
HG02896 | hp2 | a0001 | c0015 | t0001 | g0101 | AFR | GWD | FN1_chr2_215355865_215441068 | FN1 | chr2 | 215355865 | 215441068 |
HG02897 | hp1 | a0001 | c0015 | t0001 | g0103 | AFR | GWD | FN1_chr2_215355865_215441068 | FN1 | chr2 | 215355865 | 215441068 |
HG02897 | hp2 | a0001 | c0006 | t0003 | g0096 | AFR | GWD | FN1_chr2_215355865_215441068 | FN1 | chr2 | 215355865 | 215441068 |
HG02922 | hp1 | a0001 | c0015 | t0001 | g0102 | AFR | ESN | FN1_chr2_215355865_215441068 | FN1 | chr2 | 215355865 | 215441068 |
HG02922 | hp2 | a0004 | c0019 | t0001 | g0004 | AFR | ESN | FN1_chr2_215355865_215441068 | FN1 | chr2 | 215355865 | 215441068 |
HG02965 | hp1 | a0001 | c0005 | t0001 | g0179 | AFR | ESN | FN1_chr2_215355865_215441068 | FN1 | chr2 | 215355865 | 215441068 |
HG02965 | hp2 | a0006 | c0024 | t0001 | g0061 | AFR | ESN | FN1_chr2_215355865_215441068 | FN1 | chr2 | 215355865 | 215441068 |
HG02970 | hp1 | a0004 | c0020 | t0002 | g0005 | AFR | ESN | FN1_chr2_215355865_215441068 | FN1 | chr2 | 215355865 | 215441068 |
HG02970 | hp2 | a0005 | c0029 | t0003 | g0234 | AFR | ESN | FN1_chr2_215355865_215441068 | FN1 | chr2 | 215355865 | 215441068 |
HG02976 | hp1 | a0002 | c0014 | t0001 | g0054 | AFR | ESN | FN1_chr2_215355865_215441068 | FN1 | chr2 | 215355865 | 215441068 |
HG02976 | hp2 | a0003 | c0007 | t0002 | g0158 | AFR | ESN | FN1_chr2_215355865_215441068 | FN1 | chr2 | 215355865 | 215441068 |
HG03017 | hp1 | a0002 | c0008 | t0001 | g0041 | SAS | PJL | FN1_chr2_215355865_215441068 | FN1 | chr2 | 215355865 | 215441068 |
HG03017 | hp2 | a0014 | c0049 | t0001 | g0194 | SAS | PJL | FN1_chr2_215355865_215441068 | FN1 | chr2 | 215355865 | 215441068 |
HG03098 | hp1 | a0001 | c0002 | t0001 | g0141 | AFR | MSL | FN1_chr2_215355865_215441068 | FN1 | chr2 | 215355865 | 215441068 |
HG03098 | hp2 | a0003 | c0007 | t0001 | g0160 | AFR | MSL | FN1_chr2_215355865_215441068 | FN1 | chr2 | 215355865 | 215441068 |
HG03139 | hp1 | a0007 | c0017 | t0001 | g0146 | AFR | ESN | FN1_chr2_215355865_215441068 | FN1 | chr2 | 215355865 | 215441068 |
HG03139 | hp2 | a0001 | c0002 | t0001 | g0139 | AFR | ESN | FN1_chr2_215355865_215441068 | FN1 | chr2 | 215355865 | 215441068 |
HG03195 | hp1 | a0002 | c0037 | t0001 | g0058 | AFR | ESN | FN1_chr2_215355865_215441068 | FN1 | chr2 | 215355865 | 215441068 |
HG03195 | hp2 | a0001 | c0002 | t0001 | g0145 | AFR | ESN | FN1_chr2_215355865_215441068 | FN1 | chr2 | 215355865 | 215441068 |
HG03209 | hp1 | a0001 | c0002 | t0001 | g0133 | AFR | MSL | FN1_chr2_215355865_215441068 | FN1 | chr2 | 215355865 | 215441068 |
HG03209 | hp2 | a0011 | c0026 | t0001 | g0161 | AFR | MSL | FN1_chr2_215355865_215441068 | FN1 | chr2 | 215355865 | 215441068 |
HG03225 | hp1 | a0005 | c0029 | t0003 | g0235 | AFR | MSL | FN1_chr2_215355865_215441068 | FN1 | chr2 | 215355865 | 215441068 |
HG03225 | hp2 | a0001 | c0062 | t0003 | g0136 | AFR | MSL | FN1_chr2_215355865_215441068 | FN1 | chr2 | 215355865 | 215441068 |
HG03239 | hp1 | a0001 | c0004 | t0001 | g0087 | SAS | PJL | FN1_chr2_215355865_215441068 | FN1 | chr2 | 215355865 | 215441068 |
HG03239 | hp2 | a0001 | c0052 | t0001 | g0195 | SAS | PJL | FN1_chr2_215355865_215441068 | FN1 | chr2 | 215355865 | 215441068 |
HG03453 | hp1 | a0003 | c0007 | t0002 | g0156 | AFR | MSL | FN1_chr2_215355865_215441068 | FN1 | chr2 | 215355865 | 215441068 |
HG03453 | hp2 | a0001 | c0060 | t0001 | g0132 | AFR | MSL | FN1_chr2_215355865_215441068 | FN1 | chr2 | 215355865 | 215441068 |
HG03486 | hp1 | a0001 | c0002 | t0001 | g0140 | AFR | MSL | FN1_chr2_215355865_215441068 | FN1 | chr2 | 215355865 | 215441068 |
HG03486 | hp2 | a0006 | c0040 | t0001 | g0060 | AFR | MSL | FN1_chr2_215355865_215441068 | FN1 | chr2 | 215355865 | 215441068 |
HG03491 | hp1 | a0001 | c0001 | t0001 | g0188 | SAS | PJL | FN1_chr2_215355865_215441068 | FN1 | chr2 | 215355865 | 215441068 |
HG03491 | hp2 | a0001 | c0002 | t0001 | g0232 | SAS | PJL | FN1_chr2_215355865_215441068 | FN1 | chr2 | 215355865 | 215441068 |
HG03492 | hp1 | a0001 | c0002 | t0001 | g0233 | SAS | PJL | FN1_chr2_215355865_215441068 | FN1 | chr2 | 215355865 | 215441068 |
HG03492 | hp2 | a0001 | c0004 | t0001 | g0231 | SAS | PJL | FN1_chr2_215355865_215441068 | FN1 | chr2 | 215355865 | 215441068 |
HG03516 | hp1 | a0007 | c0017 | t0001 | g0076 | AFR | ESN | FN1_chr2_215355865_215441068 | FN1 | chr2 | 215355865 | 215441068 |
HG03516 | hp2 | a0010 | c0028 | t0002 | g0238 | AFR | ESN | FN1_chr2_215355865_215441068 | FN1 | chr2 | 215355865 | 215441068 |
HG03540 | hp1 | a0001 | c0041 | t0001 | g0147 | AFR | GWD | FN1_chr2_215355865_215441068 | FN1 | chr2 | 215355865 | 215441068 |
HG03540 | hp2 | a0001 | c0002 | t0001 | g0131 | AFR | GWD | FN1_chr2_215355865_215441068 | FN1 | chr2 | 215355865 | 215441068 |
HG03579 | hp1 | a0001 | c0001 | t0001 | g0222 | AFR | MSL | FN1_chr2_215355865_215441068 | FN1 | chr2 | 215355865 | 215441068 |
HG03579 | hp2 | a0003 | c0007 | t0002 | g0098 | AFR | MSL | FN1_chr2_215355865_215441068 | FN1 | chr2 | 215355865 | 215441068 |
HG03654 | hp1 | a0001 | c0002 | t0001 | g0128 | SAS | PJL | FN1_chr2_215355865_215441068 | FN1 | chr2 | 215355865 | 215441068 |
HG03654 | hp2 | a0001 | c0004 | t0001 | g0082 | SAS | PJL | FN1_chr2_215355865_215441068 | FN1 | chr2 | 215355865 | 215441068 |
HG03669 | hp1 | a0001 | c0012 | t0001 | g0089 | SAS | PJL | FN1_chr2_215355865_215441068 | FN1 | chr2 | 215355865 | 215441068 |
HG03669 | hp2 | a0002 | c0022 | t0001 | g0015 | SAS | PJL | FN1_chr2_215355865_215441068 | FN1 | chr2 | 215355865 | 215441068 |
HG03688 | hp1 | a0001 | c0004 | t0001 | g0086 | SAS | STU | FN1_chr2_215355865_215441068 | FN1 | chr2 | 215355865 | 215441068 |
HG03688 | hp2 | a0002 | c0034 | t0001 | g0055 | SAS | STU | FN1_chr2_215355865_215441068 | FN1 | chr2 | 215355865 | 215441068 |
HG03704 | hp1 | a0002 | c0033 | t0001 | g0018 | SAS | PJL | FN1_chr2_215355865_215441068 | FN1 | chr2 | 215355865 | 215441068 |
HG03704 | hp2 | a0002 | c0003 | t0001 | g0036 | SAS | PJL | FN1_chr2_215355865_215441068 | FN1 | chr2 | 215355865 | 215441068 |
HG03831 | hp1 | a0001 | c0001 | t0001 | g0189 | SAS | BEB | FN1_chr2_215355865_215441068 | FN1 | chr2 | 215355865 | 215441068 |
HG03831 | hp2 | a0017 | c0039 | t0001 | g0031 | SAS | BEB | FN1_chr2_215355865_215441068 | FN1 | chr2 | 215355865 | 215441068 |
HG03942 | hp1 | a0001 | c0001 | t0001 | g0171 | SAS | BEB | FN1_chr2_215355865_215441068 | FN1 | chr2 | 215355865 | 215441068 |
HG03942 | hp2 | a0002 | c0003 | t0001 | g0029 | SAS | BEB | FN1_chr2_215355865_215441068 | FN1 | chr2 | 215355865 | 215441068 |
HG04115 | hp1 | a0001 | c0004 | t0001 | g0085 | SAS | STU | FN1_chr2_215355865_215441068 | FN1 | chr2 | 215355865 | 215441068 |
HG04115 | hp2 | a0002 | c0003 | t0001 | g0026 | SAS | STU | FN1_chr2_215355865_215441068 | FN1 | chr2 | 215355865 | 215441068 |
HG04199 | hp1 | a0001 | c0005 | t0001 | g0218 | SAS | STU | FN1_chr2_215355865_215441068 | FN1 | chr2 | 215355865 | 215441068 |
HG04199 | hp2 | a0008 | c0018 | t0001 | g0116 | SAS | STU | FN1_chr2_215355865_215441068 | FN1 | chr2 | 215355865 | 215441068 |
HG04204 | hp1 | a0019 | c0036 | t0001 | g0038 | SAS | STU | FN1_chr2_215355865_215441068 | FN1 | chr2 | 215355865 | 215441068 |
HG04204 | hp2 | a0001 | c0001 | t0001 | g0204 | SAS | STU | FN1_chr2_215355865_215441068 | FN1 | chr2 | 215355865 | 215441068 |
HG04228 | hp1 | a0002 | c0003 | t0001 | g0030 | SAS | STU | FN1_chr2_215355865_215441068 | FN1 | chr2 | 215355865 | 215441068 |
HG04228 | hp2 | a0001 | c0001 | t0001 | g0169 | SAS | STU | FN1_chr2_215355865_215441068 | FN1 | chr2 | 215355865 | 215441068 |
NA18522 | hp1 | a0001 | c0012 | t0001 | g0154 | AFR | YRI | FN1_chr2_215355865_215441068 | FN1 | chr2 | 215355865 | 215441068 |
NA18522 | hp2 | a0005 | c0065 | t0001 | g0236 | AFR | YRI | FN1_chr2_215355865_215441068 | FN1 | chr2 | 215355865 | 215441068 |
NA18747 | hp1 | a0001 | c0054 | t0001 | g0180 | EAS | CHB | FN1_chr2_215355865_215441068 | FN1 | chr2 | 215355865 | 215441068 |
NA18747 | hp2 | a0001 | c0001 | t0001 | g0149 | EAS | CHB | FN1_chr2_215355865_215441068 | FN1 | chr2 | 215355865 | 215441068 |
NA18906 | hp1 | a0003 | c0007 | t0002 | g0099 | AFR | YRI | FN1_chr2_215355865_215441068 | FN1 | chr2 | 215355865 | 215441068 |
NA18906 | hp2 | a0004 | c0020 | t0002 | g0006 | AFR | YRI | FN1_chr2_215355865_215441068 | FN1 | chr2 | 215355865 | 215441068 |
NA18943 | hp1 | a0002 | c0013 | t0001 | g0022 | EAS | JPT | FN1_chr2_215355865_215441068 | FN1 | chr2 | 215355865 | 215441068 |
NA18943 | hp2 | a0002 | c0003 | t0001 | g0044 | EAS | JPT | FN1_chr2_215355865_215441068 | FN1 | chr2 | 215355865 | 215441068 |
NA18948 | hp1 | a0001 | c0010 | t0001 | g0152 | EAS | JPT | FN1_chr2_215355865_215441068 | FN1 | chr2 | 215355865 | 215441068 |
NA18948 | hp2 | a0012 | c0047 | t0001 | g0186 | EAS | JPT | FN1_chr2_215355865_215441068 | FN1 | chr2 | 215355865 | 215441068 |
NA18952 | hp1 | a0001 | c0001 | t0001 | g0215 | EAS | JPT | FN1_chr2_215355865_215441068 | FN1 | chr2 | 215355865 | 215441068 |
NA18952 | hp2 | a0016 | c0043 | t0001 | g0168 | EAS | JPT | FN1_chr2_215355865_215441068 | FN1 | chr2 | 215355865 | 215441068 |
NA18975 | hp1 | a0002 | c0003 | t0001 | g0042 | EAS | JPT | FN1_chr2_215355865_215441068 | FN1 | chr2 | 215355865 | 215441068 |
NA18975 | hp2 | a0001 | c0005 | t0001 | g0191 | EAS | JPT | FN1_chr2_215355865_215441068 | FN1 | chr2 | 215355865 | 215441068 |
NA19009 | hp1 | a0001 | c0001 | t0001 | g0206 | EAS | JPT | FN1_chr2_215355865_215441068 | FN1 | chr2 | 215355865 | 215441068 |
NA19009 | hp2 | a0015 | c0053 | t0001 | g0201 | EAS | JPT | FN1_chr2_215355865_215441068 | FN1 | chr2 | 215355865 | 215441068 |
NA19030 | hp1 | a0001 | c0002 | t0001 | g0144 | AFR | LWK | FN1_chr2_215355865_215441068 | FN1 | chr2 | 215355865 | 215441068 |
NA19030 | hp2 | a0001 | c0006 | t0001 | g0094 | AFR | LWK | FN1_chr2_215355865_215441068 | FN1 | chr2 | 215355865 | 215441068 |
NA19043 | hp1 | a0002 | c0013 | t0001 | g0009 | AFR | LWK | FN1_chr2_215355865_215441068 | FN1 | chr2 | 215355865 | 215441068 |
NA19043 | hp2 | a0001 | c0006 | t0001 | g0110 | AFR | LWK | FN1_chr2_215355865_215441068 | FN1 | chr2 | 215355865 | 215441068 |
NA19055 | hp1 | a0002 | c0008 | t0001 | g0043 | EAS | JPT | FN1_chr2_215355865_215441068 | FN1 | chr2 | 215355865 | 215441068 |
NA19055 | hp2 | a0001 | c0001 | t0001 | g0183 | EAS | JPT | FN1_chr2_215355865_215441068 | FN1 | chr2 | 215355865 | 215441068 |
NA19057 | hp1 | a0002 | c0003 | t0001 | g0047 | EAS | JPT | FN1_chr2_215355865_215441068 | FN1 | chr2 | 215355865 | 215441068 |
NA19057 | hp2 | a0001 | c0001 | t0001 | g0185 | EAS | JPT | FN1_chr2_215355865_215441068 | FN1 | chr2 | 215355865 | 215441068 |
NA19060 | hp1 | a0001 | c0001 | t0001 | g0151 | EAS | JPT | FN1_chr2_215355865_215441068 | FN1 | chr2 | 215355865 | 215441068 |
NA19060 | hp2 | a0001 | c0001 | t0001 | g0200 | EAS | JPT | FN1_chr2_215355865_215441068 | FN1 | chr2 | 215355865 | 215441068 |
NA19076 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | FN1_chr2_215355865_215441068 | FN1 | chr2 | 215355865 | 215441068 |
NA19076 | hp2 | a0002 | c0008 | t0001 | g0046 | EAS | JPT | FN1_chr2_215355865_215441068 | FN1 | chr2 | 215355865 | 215441068 |
NA19240 | hp1 | a0003 | c0007 | t0002 | g0066 | AFR | YRI | FN1_chr2_215355865_215441068 | FN1 | chr2 | 215355865 | 215441068 |
NA19240 | hp2 | a0001 | c0005 | t0001 | g0228 | AFR | YRI | FN1_chr2_215355865_215441068 | FN1 | chr2 | 215355865 | 215441068 |
NA20752 | hp1 | a0002 | c0021 | t0001 | g0025 | EUR | TSI | FN1_chr2_215355865_215441068 | FN1 | chr2 | 215355865 | 215441068 |
NA20752 | hp2 | a0001 | c0012 | t0001 | g0170 | EUR | TSI | FN1_chr2_215355865_215441068 | FN1 | chr2 | 215355865 | 215441068 |
NA20805 | hp1 | a0002 | c0003 | t0001 | g0016 | EUR | TSI | FN1_chr2_215355865_215441068 | FN1 | chr2 | 215355865 | 215441068 |
NA20805 | hp2 | a0001 | c0027 | t0001 | g0063 | EUR | TSI | FN1_chr2_215355865_215441068 | FN1 | chr2 | 215355865 | 215441068 |
NA20905 | hp1 | a0002 | c0003 | t0001 | g0034 | SAS | GIH | FN1_chr2_215355865_215441068 | FN1 | chr2 | 215355865 | 215441068 |
NA20905 | hp2 | a0001 | c0011 | t0001 | g0108 | SAS | GIH | FN1_chr2_215355865_215441068 | FN1 | chr2 | 215355865 | 215441068 |
HG02109 | hp1 | a0006 | c0024 | t0001 | g0059 | AFR | ACB | FN1_chr2_215355865_215441068 | FN1 | chr2 | 215355865 | 215441068 |
HG02109 | hp2 | a0001 | c0058 | t0002 | g0153 | AFR | ACB | FN1_chr2_215355865_215441068 | FN1 | chr2 | 215355865 | 215441068 |
HG02486 | hp1 | a0003 | c0056 | t0002 | g0097 | AFR | ACB | FN1_chr2_215355865_215441068 | FN1 | chr2 | 215355865 | 215441068 |
HG02486 | hp2 | a0001 | c0002 | t0001 | g0142 | AFR | ACB | FN1_chr2_215355865_215441068 | FN1 | chr2 | 215355865 | 215441068 |
HG02559 | hp1 | a0002 | c0023 | t0001 | g0049 | AFR | ACB | FN1_chr2_215355865_215441068 | FN1 | chr2 | 215355865 | 215441068 |
HG02559 | hp2 | a0003 | c0007 | t0002 | g0159 | AFR | ACB | FN1_chr2_215355865_215441068 | FN1 | chr2 | 215355865 | 215441068 |
HG03471 | hp1 | a0011 | c0026 | t0001 | g0172 | AFR | MSL | FN1_chr2_215355865_215441068 | FN1 | chr2 | 215355865 | 215441068 |
HG03471 | hp2 | a0001 | c0009 | t0002 | g0167 | AFR | MSL | FN1_chr2_215355865_215441068 | FN1 | chr2 | 215355865 | 215441068 |
HG06807 | hp1 | a0001 | c0055 | t0001 | g0078 | AFR | USA | FN1_chr2_215355865_215441068 | FN1 | chr2 | 215355865 | 215441068 |
HG06807 | hp2 | a0001 | c0006 | t0004 | g0003 | AFR | USA | FN1_chr2_215355865_215441068 | FN1 | chr2 | 215355865 | 215441068 |
NA20300 | hp1 | a0001 | c0002 | t0001 | g0124 | AFR | USA | FN1_chr2_215355865_215441068 | FN1 | chr2 | 215355865 | 215441068 |
NA20300 | hp2 | a0001 | c0009 | t0003 | g0064 | AFR | USA | FN1_chr2_215355865_215441068 | FN1 | chr2 | 215355865 | 215441068 |
NA21309 | hp1 | a0001 | c0004 | t0001 | g0071 | AFR | LWK | FN1_chr2_215355865_215441068 | FN1 | chr2 | 215355865 | 215441068 |
NA21309 | hp2 | a0001 | c0042 | t0001 | g0148 | AFR | LWK | FN1_chr2_215355865_215441068 | FN1 | chr2 | 215355865 | 215441068 |
homoSapiens_chm13v2 | hp1 | a0001 | c0002 | t0001 | g0122 | REF | REF | FN1_chr2_215355865_215441068 | FN1 | chr2 | 215355865 | 215441068 |
homoSapiens_grch38 | hp1 | a0020 | c0035 | t0001 | g0020 | REF | REF | FN1_chr2_215355865_215441068 | FN1 | chr2 | 215355865 | 215441068 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr2:215367958
|
A | G | 1 | a0014 | 1 | HG03017.hp2 | missense_variant | MODERATE | c.6923T>C | p.Val2308Ala | FN1 | ENSG00000115414.21 | transcript | ENST00000354785.11 | protein_coding | 42/46 | 7189/8390 | 6923/7434 | 2308/2477 | chr2 | 215367958 | ||
chr2:215370323
|
C | T | 3 | a0003a0010a0018 | 14 | HG02257.hp2 HG02486.hp1 HG02559.hp2 others(11): Show |
missense_variant | MODERATE | c.6824G>A | p.Arg2275Gln | FN1 | ENSG00000115414.21 | transcript | ENST00000354785.11 | protein_coding | 41/46 | 7090/8390 | 6824/7434 | 2275/2477 | chr2 | 215370323 | ||
chr2:215370366
|
C | T | 19 | a0001a0002a0003others(16): Show | 239 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(236): Show |
missense_variant | MODERATE | c.6781G>A | p.Val2261Ile | FN1 | ENSG00000115414.21 | transcript | ENST00000354785.11 | protein_coding | 41/46 | 7047/8390 | 6781/7434 | 2261/2477 | chr2 | 215370366 | ||
chr2:215371989
|
T | C | 1 | a0008 | 3 | HG01255.hp2 HG01361.hp2 HG04199.hp2 |
missense_variant | MODERATE | c.6634A>G | p.Ile2212Val | FN1 | ENSG00000115414.21 | transcript | ENST00000354785.11 | protein_coding | 40/46 | 6900/8390 | 6634/7434 | 2212/2477 | chr2 | 215371989 | ||
chr2:215378215
|
C | G | 1 | a0013 | 1 | HG02055.hp1 | missense_variant | MODERATE | c.5670G>C | p.Leu1890Phe | FN1 | ENSG00000115414.21 | transcript | ENST00000354785.11 | protein_coding | 35/46 | 5936/8390 | 5670/7434 | 1890/2477 | chr2 | 215378215 | ||
chr2:215384113
|
G | A | 1 | a0011 | 2 | HG03209.hp2 HG03471.hp1 |
missense_variant | MODERATE | c.4801C>T | p.Pro1601Ser | FN1 | ENSG00000115414.21 | transcript | ENST00000354785.11 | protein_coding | 30/46 | 5067/8390 | 4801/7434 | 1601/2477 | chr2 | 215384113 | ||
chr2:215384155
|
C | T | 1 | a0012 | 1 | NA18948.hp2 | missense_variant | MODERATE | c.4759G>A | p.Val1587Met | FN1 | ENSG00000115414.21 | transcript | ENST00000354785.11 | protein_coding | 30/46 | 5025/8390 | 4759/7434 | 1587/2477 | chr2 | 215384155 | ||
chr2:215391665
|
T | C | 1 | a0009 | 3 | HG01257.hp2 HG01258.hp2 HG01952.hp2 |
missense_variant | MODERATE | c.4219A>G | p.Ile1407Val | FN1 | ENSG00000115414.21 | transcript | ENST00000354785.11 | protein_coding | 26/46 | 4485/8390 | 4219/7434 | 1407/2477 | chr2 | 215391665 | ||
chr2:215399298
|
T | G | 1 | a0015 | 1 | NA19009.hp2 | missense_variant | MODERATE | c.3307A>C | p.Ile1103Leu | FN1 | ENSG00000115414.21 | transcript | ENST00000354785.11 | protein_coding | 21/46 | 3573/8390 | 3307/7434 | 1103/2477 | chr2 | 215399298 | ||
chr2:215404524
|
T | C | 1 | a0017 | 1 | HG03831.hp2 | missense_variant | MODERATE | c.3118A>G | p.Arg1040Gly | FN1 | ENSG00000115414.21 | transcript | ENST00000354785.11 | protein_coding | 20/46 | 3384/8390 | 3118/7434 | 1040/2477 | chr2 | 215404524 | ||
chr2:215406447
|
A | G | 1 | a0019 | 1 | HG04204.hp1 | missense_variant | MODERATE | c.2777T>C | p.Met926Thr | FN1 | ENSG00000115414.21 | transcript | ENST00000354785.11 | protein_coding | 19/46 | 3043/8390 | 2777/7434 | 926/2477 | chr2 | 215406447 | ||
chr2:215408177
|
T | G | 19 | a0001a0002a0003others(16): Show | 239 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(236): Show |
missense_variant | MODERATE | c.2449A>C | p.Thr817Pro | FN1 | ENSG00000115414.21 | transcript | ENST00000354785.11 | protein_coding | 17/46 | 2715/8390 | 2449/7434 | 817/2477 | chr2 | 215408177 | ||
chr2:215409733
|
G | A | 1 | a0007 | 3 | HG02273.hp1 HG03139.hp1 HG03516.hp1 |
missense_variant | MODERATE | c.2129C>T | p.Thr710Ile | FN1 | ENSG00000115414.21 | transcript | ENST00000354785.11 | protein_coding | 15/46 | 2395/8390 | 2129/7434 | 710/2477 | chr2 | 215409733 | ||
chr2:215428299
|
A | G | 1 | a0016 | 1 | NA18952.hp2 | missense_variant | MODERATE | c.725T>C | p.Ile242Thr | FN1 | ENSG00000115414.21 | transcript | ENST00000354785.11 | protein_coding | 6/46 | 991/8390 | 725/7434 | 242/2477 | chr2 | 215428299 | ||
chr2:215435682
|
A | C | 1 | a0006 | 3 | HG02109.hp1 HG02965.hp2 HG03486.hp2 |
missense_variant | MODERATE | c.121T>G | p.Ser41Ala | FN1 | ENSG00000115414.21 | transcript | ENST00000354785.11 | protein_coding | 1/46 | 387/8390 | 121/7434 | 41/2477 | chr2 | 215435682 | ||
chr2:215435747
|
G | A | 2 | a0005a0010 | 5 | HG02886.hp1 HG02970.hp2 HG03225.hp1 others(2): Show |
missense_variant | MODERATE | c.56C>T | p.Thr19Ile | FN1 | ENSG00000115414.21 | transcript | ENST00000354785.11 | protein_coding | 1/46 | 322/8390 | 56/7434 | 19/2477 | chr2 | 215435747 | ||
chr2:215435759
|
T | A | 15 | a0001a0003a0004others(12): Show | 189 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(186): Show |
missense_variant | MODERATE | c.44A>T | p.Gln15Leu | FN1 | ENSG00000115414.21 | transcript | ENST00000354785.11 | protein_coding | 1/46 | 310/8390 | 44/7434 | 15/2477 | chr2 | 215435759 | ||
chr2:215435763
|
C | G | 1 | a0004 | 4 | HG02647.hp1 HG02922.hp2 HG02970.hp1 others(1): Show |
missense_variant | MODERATE | c.40G>C | p.Val14Leu | FN1 | ENSG00000115414.21 | transcript | ENST00000354785.11 | protein_coding | 1/46 | 306/8390 | 40/7434 | 14/2477 | chr2 | 215435763 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr2:215364969
|
A | G | 17 | a0001c0010a0001c0011a0001c0012others(14): Show | 51 | HG00099.hp1 HG00609.hp1 HG00639.hp1 others(48): Show |
synonymous_variant | LOW | c.7161T>C | p.Tyr2387Tyr | FN1 | ENSG00000115414.21 | transcript | ENST00000354785.11 | protein_coding | 44/46 | 7427/8390 | 7161/7434 | 2387/2477 | chr2 | 215364969 | ||
chr2:215376592
|
C | T | 1 | a0003c0056 | 1 | HG02486.hp1 | synonymous_variant | LOW | c.5793G>A | p.Thr1931Thr | FN1 | ENSG00000115414.21 | transcript | ENST00000354785.11 | protein_coding | 36/46 | 6059/8390 | 5793/7434 | 1931/2477 | chr2 | 215376592 | ||
chr2:215378194
|
T | A | 13 | a0001c0001a0001c0042a0001c0050others(10): Show | 57 | HG00280.hp2 HG00609.hp2 HG00639.hp2 others(54): Show |
synonymous_variant | LOW | c.5691A>T | p.Gly1897Gly | FN1 | ENSG00000115414.21 | transcript | ENST00000354785.11 | protein_coding | 35/46 | 5957/8390 | 5691/7434 | 1897/2477 | chr2 | 215378194 | ||
chr2:215380971
|
C | A | 1 | a0002c0022 | 2 | HG01952.hp1 HG03669.hp2 |
synonymous_variant | LOW | c.5274G>T | p.Ser1758Ser | FN1 | ENSG00000115414.21 | transcript | ENST00000354785.11 | protein_coding | 33/46 | 5540/8390 | 5274/7434 | 1758/2477 | chr2 | 215380971 | ||
chr2:215384864
|
C | T | 49 | a0001c0001a0001c0002a0001c0004others(46): Show | 203 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(200): Show |
synonymous_variant | LOW | c.4725G>A | p.Glu1575Glu | FN1 | ENSG00000115414.21 | transcript | ENST00000354785.11 | protein_coding | 29/46 | 4991/8390 | 4725/7434 | 1575/2477 | chr2 | 215384864 | ||
chr2:215391666
|
T | C | 1 | a0006c0040 | 1 | HG03486.hp2 | synonymous_variant | LOW | c.4218A>G | p.Ser1406Ser | FN1 | ENSG00000115414.21 | transcript | ENST00000354785.11 | protein_coding | 26/46 | 4484/8390 | 4218/7434 | 1406/2477 | chr2 | 215391666 | ||
chr2:215391720
|
G | A | 1 | a0001c0052 | 1 | HG03239.hp2 | synonymous_variant | LOW | c.4164C>T | p.Asn1388Asn | FN1 | ENSG00000115414.21 | transcript | ENST00000354785.11 | protein_coding | 26/46 | 4430/8390 | 4164/7434 | 1388/2477 | chr2 | 215391720 | ||
chr2:215391738
|
T | C | 1 | a0001c0041 | 1 | HG03540.hp1 | synonymous_variant | LOW | c.4146A>G | p.Pro1382Pro | FN1 | ENSG00000115414.21 | transcript | ENST00000354785.11 | protein_coding | 26/46 | 4412/8390 | 4146/7434 | 1382/2477 | chr2 | 215391738 | ||
chr2:215393163
|
G | A | 2 | a0001c0041a0001c0058 | 2 | HG02109.hp2 HG03540.hp1 |
synonymous_variant | LOW | c.3837C>T | p.Thr1279Thr | FN1 | ENSG00000115414.21 | transcript | ENST00000354785.11 | protein_coding | 25/46 | 4103/8390 | 3837/7434 | 1279/2477 | chr2 | 215393163 | ||
chr2:215404453
|
G | A | 2 | a0002c0023a0018c0038 | 3 | HG01891.hp2 HG02257.hp2 HG02559.hp1 |
synonymous_variant | LOW | c.3189C>T | p.Thr1063Thr | FN1 | ENSG00000115414.21 | transcript | ENST00000354785.11 | protein_coding | 20/46 | 3455/8390 | 3189/7434 | 1063/2477 | chr2 | 215404453 | ||
chr2:215404486
|
T | G | 17 | a0001c0004a0001c0012a0001c0042others(14): Show | 62 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(59): Show |
synonymous_variant | LOW | c.3156A>C | p.Pro1052Pro | FN1 | ENSG00000115414.21 | transcript | ENST00000354785.11 | protein_coding | 20/46 | 3422/8390 | 3156/7434 | 1052/2477 | chr2 | 215404486 | ||
chr2:215404531
|
T | G | 17 | a0001c0004a0001c0012a0001c0042others(14): Show | 62 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(59): Show |
synonymous_variant | LOW | c.3111A>C | p.Gly1037Gly | FN1 | ENSG00000115414.21 | transcript | ENST00000354785.11 | protein_coding | 20/46 | 3377/8390 | 3111/7434 | 1037/2477 | chr2 | 215404531 | ||
chr2:215406389
|
G | A | 1 | a0001c0058 | 1 | HG02109.hp2 | synonymous_variant | LOW | c.2835C>T | p.Asn945Asn | FN1 | ENSG00000115414.21 | transcript | ENST00000354785.11 | protein_coding | 19/46 | 3101/8390 | 2835/7434 | 945/2477 | chr2 | 215406389 | ||
chr2:215406416
|
G | C | 1 | a0001c0055 | 1 | HG06807.hp1 | synonymous_variant | LOW | c.2808C>G | p.Gly936Gly | FN1 | ENSG00000115414.21 | transcript | ENST00000354785.11 | protein_coding | 19/46 | 3074/8390 | 2808/7434 | 936/2477 | chr2 | 215406416 | ||
chr2:215407248
|
G | A | 2 | a0001c0015a0013c0061 | 5 | HG02055.hp1 HG02622.hp2 HG02896.hp2 others(2): Show |
synonymous_variant | LOW | c.2592C>T | p.Ser864Ser | FN1 | ENSG00000115414.21 | transcript | ENST00000354785.11 | protein_coding | 18/46 | 2858/8390 | 2592/7434 | 864/2477 | chr2 | 215407248 | ||
chr2:215407302
|
C | T | 1 | a0001c0062 | 1 | HG03225.hp2 | synonymous_variant | LOW | c.2538G>A | p.Ser846Ser | FN1 | ENSG00000115414.21 | transcript | ENST00000354785.11 | protein_coding | 18/46 | 2804/8390 | 2538/7434 | 846/2477 | chr2 | 215407302 | ||
chr2:215408184
|
A | T | 25 | a0001c0001a0001c0005a0001c0010others(22): Show | 89 | HG00099.hp2 HG00280.hp2 HG00609.hp1 others(86): Show |
synonymous_variant | LOW | c.2442T>A | p.Pro814Pro | FN1 | ENSG00000115414.21 | transcript | ENST00000354785.11 | protein_coding | 17/46 | 2708/8390 | 2442/7434 | 814/2477 | chr2 | 215408184 | ||
chr2:215419324
|
A | G | 1 | a0002c0031 | 1 | HG01496.hp1 | synonymous_variant | LOW | c.1737T>C | p.Tyr579Tyr | FN1 | ENSG00000115414.21 | transcript | ENST00000354785.11 | protein_coding | 12/46 | 2003/8390 | 1737/7434 | 579/2477 | chr2 | 215419324 | ||
chr2:215422107
|
G | A | 2 | a0001c0025a0001c0046 | 3 | HG02055.hp2 HG02258.hp1 HG02723.hp1 |
synonymous_variant | LOW | c.1530C>T | p.Ala510Ala | FN1 | ENSG00000115414.21 | transcript | ENST00000354785.11 | protein_coding | 10/46 | 1796/8390 | 1530/7434 | 510/2477 | chr2 | 215422107 | ||
chr2:215422212
|
C | G | 2 | a0001c0025a0001c0046 | 3 | HG02055.hp2 HG02258.hp1 HG02723.hp1 |
synonymous_variant | LOW | c.1425G>C | p.Gly475Gly | FN1 | ENSG00000115414.21 | transcript | ENST00000354785.11 | protein_coding | 10/46 | 1691/8390 | 1425/7434 | 475/2477 | chr2 | 215422212 | ||
chr2:215424252
|
C | T | 1 | a0001c0045 | 1 | HG02723.hp2 | synonymous_variant | LOW | c.1110G>A | p.Thr370Thr | FN1 | ENSG00000115414.21 | transcript | ENST00000354785.11 | protein_coding | 8/46 | 1376/8390 | 1110/7434 | 370/2477 | chr2 | 215424252 | ||
chr2:215424261
|
A | G | 6 | a0001c0044a0004c0019a0004c0020others(3): Show | 10 | HG02258.hp2 HG02647.hp1 HG02886.hp1 others(7): Show |
synonymous_variant | LOW | c.1101T>C | p.Asn367Asn | FN1 | ENSG00000115414.21 | transcript | ENST00000354785.11 | protein_coding | 8/46 | 1367/8390 | 1101/7434 | 367/2477 | chr2 | 215424261 | ||
chr2:215425107
|
G | A | 1 | a0001c0059 | 1 | HG01975.hp2 | synonymous_variant | LOW | c.1023C>T | p.Ser341Ser | FN1 | ENSG00000115414.21 | transcript | ENST00000354785.11 | protein_coding | 7/46 | 1289/8390 | 1023/7434 | 341/2477 | chr2 | 215425107 | ||
chr2:215425128
|
C | T | 1 | a0002c0030 | 1 | HG00280.hp1 | synonymous_variant | LOW | c.1002G>A | p.Thr334Thr | FN1 | ENSG00000115414.21 | transcript | ENST00000354785.11 | protein_coding | 7/46 | 1268/8390 | 1002/7434 | 334/2477 | chr2 | 215425128 | ||
chr2:215425188
|
C | T | 1 | a0001c0060 | 1 | HG03453.hp2 | synonymous_variant | LOW | c.942G>A | p.Val314Val | FN1 | ENSG00000115414.21 | transcript | ENST00000354785.11 | protein_coding | 7/46 | 1208/8390 | 942/7434 | 314/2477 | chr2 | 215425188 | ||
chr2:215433361
|
G | A | 10 | a0001c0002a0001c0027a0001c0060others(7): Show | 41 | HG00140.hp2 HG00323.hp2 HG00642.hp2 others(38): Show |
synonymous_variant | LOW | c.378C>T | p.Ile126Ile | FN1 | ENSG00000115414.21 | transcript | ENST00000354785.11 | protein_coding | 3/46 | 644/8390 | 378/7434 | 126/2477 | chr2 | 215433361 | ||
chr2:215434774
|
G | T | 2 | a0001c0041a0001c0042 | 2 | HG03540.hp1 NA21309.hp2 |
synonymous_variant | LOW | c.199C>A | p.Arg67Arg | FN1 | ENSG00000115414.21 | transcript | ENST00000354785.11 | protein_coding | 2/46 | 465/8390 | 199/7434 | 67/2477 | chr2 | 215434774 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr2:215361003
|
T | C | 9 | a0001c0006t0002a0001c0009t0002a0001c0058t0002others(6): Show | 17 | HG02109.hp2 HG02257.hp2 HG02486.hp1 others(14): Show |
3_prime_UTR_variant | MODIFIER | c.*552A>G | FN1 | ENSG00000115414.21 | transcript | ENST00000354785.11 | protein_coding | 46/46 | 552 | chr2 | 215361003 | |||||
chr2:215361425
|
G | A | 4 | a0001c0006t0003a0001c0009t0003a0001c0062t0003others(1): Show | 7 | HG02145.hp2 HG02895.hp2 HG02897.hp2 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*130C>T | FN1 | ENSG00000115414.21 | transcript | ENST00000354785.11 | protein_coding | 46/46 | 130 | chr2 | 215361425 | |||||
chr2:215436043
|
C | T | 1 | a0001c0006t0004 | 1 | HG06807.hp2 | 5_prime_UTR_variant | MODIFIER | c.-241G>A | FN1 | ENSG00000115414.21 | transcript | ENST00000354785.11 | protein_coding | 1/46 | 241 | chr2 | 215436043 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr2:215361645
|
G | A | 1 | a0001c0044t0001g0065 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.7363-19C>T | FN1 | ENSG00000115414.21 | transcript | ENST00000354785.11 | protein_coding | 45/45 | chr2 | 215361645 | ||||||
chr2:215361656
|
T | C | 5 | a0001c0005t0001g0214a0001c0005t0001g0221a0004c0019t0001g0004others(2): Show | 5 | HG02280.hp2 HG02630.hp2 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.7363-30A>G | FN1 | ENSG00000115414.21 | transcript | ENST00000354785.11 | protein_coding | 45/45 | chr2 | 215361656 | ||||||
chr2:215361670
|
G | A | 1 | a0001c0005t0001g0178 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.7363-44C>T | FN1 | ENSG00000115414.21 | transcript | ENST00000354785.11 | protein_coding | 45/45 | chr2 | 215361670 | ||||||
chr2:215361694
|
C | CG | 5 | a0001c0005t0001g0214a0001c0005t0001g0221a0004c0019t0001g0004others(2): Show | 5 | HG02280.hp2 HG02630.hp2 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.7363-69dupC | FN1 | ENSG00000115414.21 | transcript | ENST00000354785.11 | protein_coding | 45/45 | chr2 | 215361694 | ||||||
chr2:215361786
|
T | C | 1 | a0002c0014t0001g0056 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.7363-160A>G | FN1 | ENSG00000115414.21 | transcript | ENST00000354785.11 | protein_coding | 45/45 | chr2 | 215361786 | ||||||
chr2:215361907
|
G | C | 1 | a0002c0030t0001g0017 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.7362+62C>G | FN1 | ENSG00000115414.21 | transcript | ENST00000354785.11 | protein_coding | 45/45 | chr2 | 215361907 | ||||||
chr2:215361916
|
A | G | 1 | a0001c0015t0001g0104 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.7362+53T>C | FN1 | ENSG00000115414.21 | transcript | ENST00000354785.11 | protein_coding | 45/45 | chr2 | 215361916 | ||||||
chr2:215361919
|
A | C | 47 | a0001c0001t0001g0062a0001c0001t0001g0173a0001c0001t0001g0181others(44): Show | 48 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(45): Show |
intron_variant | MODIFIER | c.7362+50T>G | FN1 | ENSG00000115414.21 | transcript | ENST00000354785.11 | protein_coding | 45/45 | chr2 | 215361919 | ||||||
chr2:215362110
|
G | A | 1 | a0001c0005t0001g0178 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.7252-31C>T | FN1 | ENSG00000115414.21 | transcript | ENST00000354785.11 | protein_coding | 44/45 | chr2 | 215362110 | ||||||
chr2:215362230
|
G | A | 3 | a0001c0004t0001g0070a0001c0009t0001g0157a0006c0024t0001g0059 | 3 | HG02109.hp1 HG02451.hp1 HG02717.hp1 |
intron_variant | MODIFIER | c.7252-151C>T | FN1 | ENSG00000115414.21 | transcript | ENST00000354785.11 | protein_coding | 44/45 | chr2 | 215362230 | ||||||
chr2:215362403
|
T | C | 1 | a0001c0001t0001g0217 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.7252-324A>G | FN1 | ENSG00000115414.21 | transcript | ENST00000354785.11 | protein_coding | 44/45 | chr2 | 215362403 | ||||||
chr2:215362410
|
G | A | 3 | a0001c0005t0001g0221a0004c0019t0001g0004a0004c0019t0001g0007 | 3 | HG02630.hp2 HG02647.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.7252-331C>T | FN1 | ENSG00000115414.21 | transcript | ENST00000354785.11 | protein_coding | 44/45 | chr2 | 215362410 | ||||||
chr2:215362463
|
A | G | 35 | a0001c0001t0001g0222a0001c0002t0001g0133a0001c0002t0001g0135others(32): Show | 35 | HG01109.hp2 HG01256.hp2 HG01258.hp1 others(32): Show |
intron_variant | MODIFIER | c.7252-384T>C | FN1 | ENSG00000115414.21 | transcript | ENST00000354785.11 | protein_coding | 44/45 | chr2 | 215362463 | ||||||
chr2:215362464
|
C | T | 35 | a0001c0001t0001g0149a0001c0001t0001g0150a0001c0001t0001g0151others(32): Show | 35 | HG00140.hp2 HG00639.hp2 HG01069.hp1 others(32): Show |
intron_variant | MODIFIER | c.7252-385G>A | FN1 | ENSG00000115414.21 | transcript | ENST00000354785.11 | protein_coding | 44/45 | chr2 | 215362464 | ||||||
chr2:215362491
|
G | A | 1 | a0001c0005t0001g0178 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.7252-412C>T | FN1 | ENSG00000115414.21 | transcript | ENST00000354785.11 | protein_coding | 44/45 | chr2 | 215362491 | ||||||
chr2:215362571
|
G | A | 2 | a0005c0029t0003g0234a0005c0029t0003g0235 | 2 | HG02970.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.7252-492C>T | FN1 | ENSG00000115414.21 | transcript | ENST00000354785.11 | protein_coding | 44/45 | chr2 | 215362571 | ||||||
chr2:215362884
|
G | A | 1 | a0001c0059t0001g0219 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.7252-805C>T | FN1 | ENSG00000115414.21 | transcript | ENST00000354785.11 | protein_coding | 44/45 | chr2 | 215362884 | ||||||
chr2:215362901
|
C | T | 1 | a0001c0012t0001g0079 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.7252-822G>A | FN1 | ENSG00000115414.21 | transcript | ENST00000354785.11 | protein_coding | 44/45 | chr2 | 215362901 | ||||||
chr2:215362902
|
C | T | 1 | a0001c0005t0001g0178 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.7252-823G>A | FN1 | ENSG00000115414.21 | transcript | ENST00000354785.11 | protein_coding | 44/45 | chr2 | 215362902 | ||||||
chr2:215362907
|
G | A | 1 | a0001c0005t0001g0178 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.7252-828C>T | FN1 | ENSG00000115414.21 | transcript | ENST00000354785.11 | protein_coding | 44/45 | chr2 | 215362907 | ||||||
chr2:215363142
|
T | C | 1 | a0002c0003t0001g0026 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.7252-1063A>G | FN1 | ENSG00000115414.21 | transcript | ENST00000354785.11 | protein_coding | 44/45 | chr2 | 215363142 | ||||||
chr2:215363224
|
G | A | 1 | a0001c0005t0001g0178 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.7252-1145C>T | FN1 | ENSG00000115414.21 | transcript | ENST00000354785.11 | protein_coding | 44/45 | chr2 | 215363224 | ||||||
chr2:215363363
|
T | C | 1 | a0012c0047t0001g0186 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.7252-1284A>G | FN1 | ENSG00000115414.21 | transcript | ENST00000354785.11 | protein_coding | 44/45 | chr2 | 215363363 | ||||||
chr2:215363377
|
GGAGA | G | 4 | a0001c0002t0001g0129a0001c0063t0001g0125a0002c0013t0001g0009others(1): Show | 4 | HG00140.hp2 HG01109.hp1 HG01496.hp2 others(1): Show |
intron_variant | MODIFIER | c.7252-1302_7252-129 others(8): Show |
FN1 | ENSG00000115414.21 | transcript | ENST00000354785.11 | protein_coding | 44/45 | chr2 | 215363377 | ||||||
chr2:215363377
|
GGAGAGA | G | 65 | a0001c0001t0001g0002a0001c0001t0001g0149a0001c0001t0001g0150others(62): Show | 66 | HG00099.hp2 HG00140.hp1 HG00609.hp2 others(63): Show |
intron_variant | MODIFIER | c.7252-1304_7252-129 others(10): Show |
FN1 | ENSG00000115414.21 | transcript | ENST00000354785.11 | protein_coding | 44/45 | chr2 | 215363377 | ||||||
chr2:215363504
|
T | C | 11 | a0001c0004t0001g0001a0001c0004t0001g0068a0001c0004t0001g0080others(8): Show | 12 | HG00280.hp1 HG00642.hp1 HG00735.hp2 others(9): Show |
intron_variant | MODIFIER | c.7251+1375A>G | FN1 | ENSG00000115414.21 | transcript | ENST00000354785.11 | protein_coding | 44/45 | chr2 | 215363504 | ||||||
chr2:215363533
|
A | G | 1 | a0001c0005t0001g0178 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.7251+1346T>C | FN1 | ENSG00000115414.21 | transcript | ENST00000354785.11 | protein_coding | 44/45 | chr2 | 215363533 | ||||||
chr2:215363728
|
G | A | 1 | a0006c0040t0001g0060 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.7251+1151C>T | FN1 | ENSG00000115414.21 | transcript | ENST00000354785.11 | protein_coding | 44/45 | chr2 | 215363728 | ||||||
chr2:215363760
|
T | TTTTA | 54 | a0001c0005t0001g0178a0001c0009t0002g0167a0001c0010t0001g0152others(51): Show | 54 | HG00099.hp1 HG00609.hp1 HG00639.hp1 others(51): Show |
intron_variant | MODIFIER | c.7251+1118_7251+111 others(8): Show |
FN1 | ENSG00000115414.21 | transcript | ENST00000354785.11 | protein_coding | 44/45 | chr2 | 215363760 | ||||||
chr2:215364212
|
A | G | 1 | a0001c0057t0001g0105 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.7251+667T>C | FN1 | ENSG00000115414.21 | transcript | ENST00000354785.11 | protein_coding | 44/45 | chr2 | 215364212 | ||||||
chr2:215364225
|
C | T | 5 | a0001c0002t0001g0137a0001c0002t0001g0141a0001c0025t0001g0163others(2): Show | 5 | HG01891.hp2 HG02451.hp2 HG02559.hp1 others(2): Show |
intron_variant | MODIFIER | c.7251+654G>A | FN1 | ENSG00000115414.21 | transcript | ENST00000354785.11 | protein_coding | 44/45 | chr2 | 215364225 | ||||||
chr2:215364333
|
T | TG | 237 | a0001c0001t0001g0002a0001c0001t0001g0062a0001c0001t0001g0149others(234): Show | 239 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(236): Show |
intron_variant | MODIFIER | c.7251+545dupC | FN1 | ENSG00000115414.21 | transcript | ENST00000354785.11 | protein_coding | 44/45 | chr2 | 215364333 | ||||||
chr2:215364356
|
G | A | 1 | a0001c0044t0001g0065 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.7251+523C>T | FN1 | ENSG00000115414.21 | transcript | ENST00000354785.11 | protein_coding | 44/45 | chr2 | 215364356 | ||||||
chr2:215364678
|
G | A | 16 | a0001c0006t0002g0077a0001c0058t0002g0153a0003c0007t0001g0088others(13): Show | 16 | HG02109.hp2 HG02257.hp2 HG02486.hp1 others(13): Show |
intron_variant | MODIFIER | c.7251+201C>T | FN1 | ENSG00000115414.21 | transcript | ENST00000354785.11 | protein_coding | 44/45 | chr2 | 215364678 | ||||||
chr2:215365127
|
C | T | 26 | a0001c0001t0001g0062a0001c0001t0001g0173a0001c0001t0001g0210others(23): Show | 26 | HG00280.hp2 HG00323.hp1 HG00323.hp2 others(23): Show |
intron_variant | MODIFIER | c.7145-142G>A | FN1 | ENSG00000115414.21 | transcript | ENST00000354785.11 | protein_coding | 43/45 | chr2 | 215365127 | ||||||
chr2:215365233
|
C | G | 1 | a0001c0044t0001g0065 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.7145-248G>C | FN1 | ENSG00000115414.21 | transcript | ENST00000354785.11 | protein_coding | 43/45 | chr2 | 215365233 | ||||||
chr2:215365308
|
T | G | 1 | a0001c0005t0001g0178 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.7144+197A>C | FN1 | ENSG00000115414.21 | transcript | ENST00000354785.11 | protein_coding | 43/45 | chr2 | 215365308 | ||||||
chr2:215365310
|
T | C | 1 | a0001c0012t0001g0079 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.7144+195A>G | FN1 | ENSG00000115414.21 | transcript | ENST00000354785.11 | protein_coding | 43/45 | chr2 | 215365310 | ||||||
chr2:215365358
|
T | C | 29 | a0001c0001t0001g0062a0001c0001t0001g0173a0001c0001t0001g0210others(26): Show | 29 | HG00280.hp2 HG00323.hp1 HG00323.hp2 others(26): Show |
intron_variant | MODIFIER | c.7144+147A>G | FN1 | ENSG00000115414.21 | transcript | ENST00000354785.11 | protein_coding | 43/45 | chr2 | 215365358 | ||||||
chr2:215365493
|
G | C | 18 | a0001c0001t0001g0181a0001c0001t0001g0192a0001c0001t0001g0193others(15): Show | 19 | HG00280.hp1 HG00642.hp1 HG00642.hp2 others(16): Show |
intron_variant | MODIFIER | c.7144+12C>G | FN1 | ENSG00000115414.21 | transcript | ENST00000354785.11 | protein_coding | 43/45 | chr2 | 215365493 | ||||||
chr2:215365780
|
T | C | 1 | a0001c0005t0001g0178 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.7019-150A>G | FN1 | ENSG00000115414.21 | transcript | ENST00000354785.11 | protein_coding | 42/45 | chr2 | 215365780 | ||||||
chr2:215365806
|
ATT | A | 96 | a0001c0001t0001g0181a0001c0001t0001g0192a0001c0001t0001g0193others(93): Show | 97 | HG00099.hp1 HG00280.hp1 HG00609.hp1 others(94): Show |
intron_variant | MODIFIER | c.7019-178_7019-177d others(4): Show |
FN1 | ENSG00000115414.21 | transcript | ENST00000354785.11 | protein_coding | 42/45 | chr2 | 215365806 | ||||||
chr2:215365806
|
ATTT | A | 10 | a0001c0001t0001g0222a0001c0006t0002g0077a0003c0007t0002g0066others(7): Show | 10 | HG02257.hp2 HG02559.hp2 HG02886.hp1 others(7): Show |
intron_variant | MODIFIER | c.7019-179_7019-177d others(5): Show |
FN1 | ENSG00000115414.21 | transcript | ENST00000354785.11 | protein_coding | 42/45 | chr2 | 215365806 | ||||||
chr2:215365810
|
T | A | 73 | a0001c0001t0001g0002a0001c0001t0001g0149a0001c0001t0001g0150others(70): Show | 74 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(71): Show |
intron_variant | MODIFIER | c.7019-180A>T | FN1 | ENSG00000115414.21 | transcript | ENST00000354785.11 | protein_coding | 42/45 | chr2 | 215365810 | ||||||
chr2:215365810
|
T | TA | 5 | a0001c0005t0001g0214a0001c0005t0001g0221a0004c0019t0001g0004others(2): Show | 5 | HG02280.hp2 HG02630.hp2 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.7019-181_7019-180i others(3): Show |
FN1 | ENSG00000115414.21 | transcript | ENST00000354785.11 | protein_coding | 42/45 | chr2 | 215365810 | ||||||
chr2:215365811
|
T | A | 32 | a0001c0001t0001g0062a0001c0001t0001g0173a0001c0001t0001g0210others(29): Show | 32 | HG00280.hp2 HG00323.hp1 HG00323.hp2 others(29): Show |
intron_variant | MODIFIER | c.7019-181A>T | FN1 | ENSG00000115414.21 | transcript | ENST00000354785.11 | protein_coding | 42/45 | chr2 | 215365811 | ||||||
chr2:215365812
|
T | A | 47 | a0001c0010t0001g0152a0001c0010t0001g0184a0001c0010t0001g0205others(44): Show | 47 | HG00099.hp1 HG00609.hp1 HG00639.hp1 others(44): Show |
intron_variant | MODIFIER | c.7019-182A>T | FN1 | ENSG00000115414.21 | transcript | ENST00000354785.11 | protein_coding | 42/45 | chr2 | 215365812 | ||||||
chr2:215365868
|
C | T | 1 | a0001c0001t0001g0183 | 1 | NA19055.hp2 | intron_variant | MODIFIER | c.7019-238G>A | FN1 | ENSG00000115414.21 | transcript | ENST00000354785.11 | protein_coding | 42/45 | chr2 | 215365868 | ||||||
chr2:215365904
|
C | T | 2 | a0001c0002t0001g0111a0001c0045t0001g0165 | 2 | HG02280.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.7019-274G>A | FN1 | ENSG00000115414.21 | transcript | ENST00000354785.11 | protein_coding | 42/45 | chr2 | 215365904 | ||||||
chr2:215365933
|
G | A | 1 | a0001c0005t0001g0178 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.7019-303C>T | FN1 | ENSG00000115414.21 | transcript | ENST00000354785.11 | protein_coding | 42/45 | chr2 | 215365933 | ||||||
chr2:215365966
|
A | AT | 48 | a0001c0001t0001g0062a0001c0001t0001g0173a0001c0002t0001g0112others(45): Show | 48 | HG00323.hp1 HG00323.hp2 HG00738.hp2 others(45): Show |
intron_variant | MODIFIER | c.7019-337dupA | FN1 | ENSG00000115414.21 | transcript | ENST00000354785.11 | protein_coding | 42/45 | chr2 | 215365966 | ||||||
chr2:215365966
|
A | ATT | 23 | a0001c0001t0001g0181a0001c0001t0001g0192a0001c0001t0001g0193others(20): Show | 24 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(21): Show |
intron_variant | MODIFIER | c.7019-338_7019-337d others(4): Show |
FN1 | ENSG00000115414.21 | transcript | ENST00000354785.11 | protein_coding | 42/45 | chr2 | 215365966 | ||||||
chr2:215365966
|
AT | A | 12 | a0001c0002t0001g0137a0001c0002t0001g0141a0001c0009t0001g0074others(9): Show | 12 | HG01167.hp2 HG01891.hp2 HG02451.hp2 others(9): Show |
intron_variant | MODIFIER | c.7019-337delA | FN1 | ENSG00000115414.21 | transcript | ENST00000354785.11 | protein_coding | 42/45 | chr2 | 215365966 | ||||||
chr2:215365966
|
ATT | A | 6 | a0001c0001t0001g0150a0001c0001t0001g0187a0001c0001t0001g0204others(3): Show | 6 | HG01261.hp2 HG02132.hp2 HG02165.hp1 others(3): Show |
intron_variant | MODIFIER | c.7019-338_7019-337d others(4): Show |
FN1 | ENSG00000115414.21 | transcript | ENST00000354785.11 | protein_coding | 42/45 | chr2 | 215365966 | ||||||
chr2:215365966
|
ATTT | A | 65 | a0001c0001t0001g0002a0001c0001t0001g0149a0001c0001t0001g0151others(62): Show | 66 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(63): Show |
intron_variant | MODIFIER | c.7019-339_7019-337d others(5): Show |
FN1 | ENSG00000115414.21 | transcript | ENST00000354785.11 | protein_coding | 42/45 | chr2 | 215365966 | ||||||
chr2:215365966
|
ATTTTTTT others(5): Show |
A | 1 | a0006c0040t0001g0060 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.7019-348_7019-337d others(14): Show |
FN1 | ENSG00000115414.21 | transcript | ENST00000354785.11 | protein_coding | 42/45 | chr2 | 215365966 | ||||||
chr2:215366195
|
A | G | 1 | a0005c0029t0003g0234 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.7019-565T>C | FN1 | ENSG00000115414.21 | transcript | ENST00000354785.11 | protein_coding | 42/45 | chr2 | 215366195 | ||||||
chr2:215366332
|
A | T | 1 | a0003c0056t0002g0097 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.7019-702T>A | FN1 | ENSG00000115414.21 | transcript | ENST00000354785.11 | protein_coding | 42/45 | chr2 | 215366332 | ||||||
chr2:215366618
|
C | T | 1 | a0001c0005t0001g0178 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.7019-988G>A | FN1 | ENSG00000115414.21 | transcript | ENST00000354785.11 | protein_coding | 42/45 | chr2 | 215366618 | ||||||
chr2:215366811
|
A | AG | 7 | a0001c0006t0003g0073a0001c0006t0003g0095a0001c0006t0003g0096others(4): Show | 7 | HG02145.hp2 HG02895.hp2 HG02897.hp2 others(4): Show |
intron_variant | MODIFIER | c.7018+1051_7018+105 others(5): Show |
FN1 | ENSG00000115414.21 | transcript | ENST00000354785.11 | protein_coding | 42/45 | chr2 | 215366811 | ||||||
chr2:215366813
|
A | T | 7 | a0001c0006t0003g0073a0001c0006t0003g0095a0001c0006t0003g0096others(4): Show | 7 | HG02145.hp2 HG02895.hp2 HG02897.hp2 others(4): Show |
intron_variant | MODIFIER | c.7018+1050T>A | FN1 | ENSG00000115414.21 | transcript | ENST00000354785.11 | protein_coding | 42/45 | chr2 | 215366813 | ||||||
chr2:215366814
|
A | T | 7 | a0001c0006t0003g0073a0001c0006t0003g0095a0001c0006t0003g0096others(4): Show | 7 | HG02145.hp2 HG02895.hp2 HG02897.hp2 others(4): Show |
intron_variant | MODIFIER | c.7018+1049T>A | FN1 | ENSG00000115414.21 | transcript | ENST00000354785.11 | protein_coding | 42/45 | chr2 | 215366814 | ||||||
chr2:215366815
|
ACAT | A | 7 | a0001c0006t0003g0073a0001c0006t0003g0095a0001c0006t0003g0096others(4): Show | 7 | HG02145.hp2 HG02895.hp2 HG02897.hp2 others(4): Show |
intron_variant | MODIFIER | c.7018+1045_7018+104 others(7): Show |
FN1 | ENSG00000115414.21 | transcript | ENST00000354785.11 | protein_coding | 42/45 | chr2 | 215366815 | ||||||
chr2:215367000
|
G | A | 18 | a0001c0001t0001g0181a0001c0001t0001g0192a0001c0001t0001g0193others(15): Show | 19 | HG00280.hp1 HG00642.hp1 HG00642.hp2 others(16): Show |
intron_variant | MODIFIER | c.7018+863C>T | FN1 | ENSG00000115414.21 | transcript | ENST00000354785.11 | protein_coding | 42/45 | chr2 | 215367000 | ||||||
chr2:215367114
|
A | C | 15 | a0001c0006t0002g0077a0003c0007t0001g0088a0003c0007t0002g0066others(12): Show | 15 | HG02257.hp2 HG02486.hp1 HG02559.hp2 others(12): Show |
intron_variant | MODIFIER | c.7018+749T>G | FN1 | ENSG00000115414.21 | transcript | ENST00000354785.11 | protein_coding | 42/45 | chr2 | 215367114 | ||||||
chr2:215367118
|
C | T | 1 | a0001c0044t0001g0065 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.7018+745G>A | FN1 | ENSG00000115414.21 | transcript | ENST00000354785.11 | protein_coding | 42/45 | chr2 | 215367118 | ||||||
chr2:215367385
|
G | A | 47 | a0001c0010t0001g0152a0001c0010t0001g0184a0001c0010t0001g0205others(44): Show | 47 | HG00099.hp1 HG00609.hp1 HG00639.hp1 others(44): Show |
intron_variant | MODIFIER | c.7018+478C>T | FN1 | ENSG00000115414.21 | transcript | ENST00000354785.11 | protein_coding | 42/45 | chr2 | 215367385 | ||||||
chr2:215367398
|
C | T | 178 | a0001c0001t0001g0002a0001c0001t0001g0149a0001c0001t0001g0150others(175): Show | 180 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(177): Show |
intron_variant | MODIFIER | c.7018+465G>A | FN1 | ENSG00000115414.21 | transcript | ENST00000354785.11 | protein_coding | 42/45 | chr2 | 215367398 | ||||||
chr2:215367549
|
A | G | 1 | a0001c0005t0001g0178 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.7018+314T>C | FN1 | ENSG00000115414.21 | transcript | ENST00000354785.11 | protein_coding | 42/45 | chr2 | 215367549 | ||||||
chr2:215367576
|
C | A | 174 | a0001c0001t0001g0002a0001c0001t0001g0149a0001c0001t0001g0150others(171): Show | 176 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(173): Show |
intron_variant | MODIFIER | c.7018+287G>T | FN1 | ENSG00000115414.21 | transcript | ENST00000354785.11 | protein_coding | 42/45 | chr2 | 215367576 | ||||||
chr2:215367640
|
T | C | 1 | a0001c0012t0001g0079 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.7018+223A>G | FN1 | ENSG00000115414.21 | transcript | ENST00000354785.11 | protein_coding | 42/45 | chr2 | 215367640 | ||||||
chr2:215367833
|
C | T | 29 | a0001c0001t0001g0062a0001c0001t0001g0173a0001c0001t0001g0210others(26): Show | 29 | HG00280.hp2 HG00323.hp1 HG00323.hp2 others(26): Show |
intron_variant | MODIFIER | c.7018+30G>A | FN1 | ENSG00000115414.21 | transcript | ENST00000354785.11 | protein_coding | 42/45 | chr2 | 215367833 | ||||||
chr2:215368085
|
TAAG | T | 5 | a0001c0002t0001g0137a0001c0002t0001g0141a0001c0025t0001g0163others(2): Show | 5 | HG01891.hp2 HG02451.hp2 HG02559.hp1 others(2): Show |
intron_variant | MODIFIER | c.6854-61_6854-59del others(3): Show |
FN1 | ENSG00000115414.21 | transcript | ENST00000354785.11 | protein_coding | 41/45 | chr2 | 215368085 | ||||||
chr2:215368206
|
G | A | 2 | a0001c0002t0001g0111a0001c0045t0001g0165 | 2 | HG02280.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.6854-179C>T | FN1 | ENSG00000115414.21 | transcript | ENST00000354785.11 | protein_coding | 41/45 | chr2 | 215368206 | ||||||
chr2:215368225
|
C | T | 2 | a0001c0002t0001g0111a0001c0045t0001g0165 | 2 | HG02280.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.6854-198G>A | FN1 | ENSG00000115414.21 | transcript | ENST00000354785.11 | protein_coding | 41/45 | chr2 | 215368225 | ||||||
chr2:215368255
|
C | A | 68 | a0001c0001t0001g0002a0001c0001t0001g0149a0001c0001t0001g0150others(65): Show | 69 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(66): Show |
intron_variant | MODIFIER | c.6854-228G>T | FN1 | ENSG00000115414.21 | transcript | ENST00000354785.11 | protein_coding | 41/45 | chr2 | 215368255 | ||||||
chr2:215368416
|
C | A | 1 | a0001c0005t0001g0178 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.6854-389G>T | FN1 | ENSG00000115414.21 | transcript | ENST00000354785.11 | protein_coding | 41/45 | chr2 | 215368416 | ||||||
chr2:215368561
|
A | G | 2 | a0001c0002t0001g0232a0001c0002t0001g0233 | 2 | HG03491.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.6854-534T>C | FN1 | ENSG00000115414.21 | transcript | ENST00000354785.11 | protein_coding | 41/45 | chr2 | 215368561 | ||||||
chr2:215368594
|
G | A | 1 | a0001c0005t0001g0178 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.6854-567C>T | FN1 | ENSG00000115414.21 | transcript | ENST00000354785.11 | protein_coding | 41/45 | chr2 | 215368594 | ||||||
chr2:215368769
|
G | T | 47 | a0001c0001t0001g0062a0001c0001t0001g0173a0001c0001t0001g0181others(44): Show | 48 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(45): Show |
intron_variant | MODIFIER | c.6854-742C>A | FN1 | ENSG00000115414.21 | transcript | ENST00000354785.11 | protein_coding | 41/45 | chr2 | 215368769 | ||||||
chr2:215368880
|
A | T | 1 | a0001c0006t0003g0073 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.6854-853T>A | FN1 | ENSG00000115414.21 | transcript | ENST00000354785.11 | protein_coding | 41/45 | chr2 | 215368880 | ||||||
chr2:215368975
|
A | G | 47 | a0001c0001t0001g0062a0001c0001t0001g0173a0001c0001t0001g0181others(44): Show | 48 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(45): Show |
intron_variant | MODIFIER | c.6854-948T>C | FN1 | ENSG00000115414.21 | transcript | ENST00000354785.11 | protein_coding | 41/45 | chr2 | 215368975 | ||||||
chr2:215368976
|
T | C | 1 | a0001c0005t0001g0178 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.6854-949A>G | FN1 | ENSG00000115414.21 | transcript | ENST00000354785.11 | protein_coding | 41/45 | chr2 | 215368976 | ||||||
chr2:215369076
|
G | A | 2 | a0001c0004t0001g0086a0001c0004t0001g0231 | 2 | HG03492.hp2 HG03688.hp1 |
intron_variant | MODIFIER | c.6854-1049C>T | FN1 | ENSG00000115414.21 | transcript | ENST00000354785.11 | protein_coding | 41/45 | chr2 | 215369076 | ||||||
chr2:215369147
|
G | A | 4 | a0001c0006t0004g0003a0001c0009t0001g0074a0001c0041t0001g0147others(1): Show | 4 | HG02055.hp2 HG02572.hp2 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.6854-1120C>T | FN1 | ENSG00000115414.21 | transcript | ENST00000354785.11 | protein_coding | 41/45 | chr2 | 215369147 | ||||||
chr2:215369161
|
A | G | 1 | a0001c0050t0001g0182 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.6853+1133T>C | FN1 | ENSG00000115414.21 | transcript | ENST00000354785.11 | protein_coding | 41/45 | chr2 | 215369161 | ||||||
chr2:215369208
|
G | A | 5 | a0001c0005t0001g0229a0002c0014t0001g0052a0002c0014t0001g0054others(2): Show | 5 | HG01884.hp2 HG02615.hp2 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.6853+1086C>T | FN1 | ENSG00000115414.21 | transcript | ENST00000354785.11 | protein_coding | 41/45 | chr2 | 215369208 | ||||||
chr2:215369215
|
T | TA | 51 | a0001c0001t0001g0062a0001c0001t0001g0173a0001c0001t0001g0181others(48): Show | 52 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(49): Show |
intron_variant | MODIFIER | c.6853+1078dupT | FN1 | ENSG00000115414.21 | transcript | ENST00000354785.11 | protein_coding | 41/45 | chr2 | 215369215 | ||||||
chr2:215369215
|
TA | T | 41 | a0001c0001t0001g0169a0001c0001t0001g0185a0001c0002t0001g0135others(38): Show | 41 | HG01109.hp2 HG01167.hp2 HG01168.hp1 others(38): Show |
intron_variant | MODIFIER | c.6853+1078delT | FN1 | ENSG00000115414.21 | transcript | ENST00000354785.11 | protein_coding | 41/45 | chr2 | 215369215 | ||||||
chr2:215369215
|
TAA | T | 7 | a0001c0002t0001g0137a0001c0002t0001g0141a0001c0025t0001g0163others(4): Show | 7 | HG01891.hp2 HG02109.hp2 HG02451.hp2 others(4): Show |
intron_variant | MODIFIER | c.6853+1077_6853+107 others(6): Show |
FN1 | ENSG00000115414.21 | transcript | ENST00000354785.11 | protein_coding | 41/45 | chr2 | 215369215 | ||||||
chr2:215369375
|
C | A | 18 | a0001c0001t0001g0181a0001c0001t0001g0192a0001c0001t0001g0193others(15): Show | 19 | HG00280.hp1 HG00642.hp1 HG00642.hp2 others(16): Show |
intron_variant | MODIFIER | c.6853+919G>T | FN1 | ENSG00000115414.21 | transcript | ENST00000354785.11 | protein_coding | 41/45 | chr2 | 215369375 | ||||||
chr2:215369443
|
T | G | 1 | a0001c0005t0001g0178 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.6853+851A>C | FN1 | ENSG00000115414.21 | transcript | ENST00000354785.11 | protein_coding | 41/45 | chr2 | 215369443 | ||||||
chr2:215369535
|
T | C | 1 | a0001c0012t0001g0154 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.6853+759A>G | FN1 | ENSG00000115414.21 | transcript | ENST00000354785.11 | protein_coding | 41/45 | chr2 | 215369535 | ||||||
chr2:215369593
|
T | C | 1 | a0001c0002t0001g0112 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.6853+701A>G | FN1 | ENSG00000115414.21 | transcript | ENST00000354785.11 | protein_coding | 41/45 | chr2 | 215369593 | ||||||
chr2:215369656
|
T | G | 2 | a0001c0005t0001g0214a0006c0040t0001g0060 | 2 | HG02280.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.6853+638A>C | FN1 | ENSG00000115414.21 | transcript | ENST00000354785.11 | protein_coding | 41/45 | chr2 | 215369656 | ||||||
chr2:215369893
|
G | A | 1 | a0001c0012t0001g0079 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.6853+401C>T | FN1 | ENSG00000115414.21 | transcript | ENST00000354785.11 | protein_coding | 41/45 | chr2 | 215369893 | ||||||
chr2:215369934
|
G | A | 35 | a0001c0001t0001g0149a0001c0001t0001g0150a0001c0001t0001g0151others(32): Show | 35 | HG00140.hp2 HG00639.hp2 HG01069.hp1 others(32): Show |
intron_variant | MODIFIER | c.6853+360C>T | FN1 | ENSG00000115414.21 | transcript | ENST00000354785.11 | protein_coding | 41/45 | chr2 | 215369934 | ||||||
chr2:215369996
|
G | C | 187 | a0001c0001t0001g0002a0001c0001t0001g0062a0001c0001t0001g0149others(184): Show | 189 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(186): Show |
intron_variant | MODIFIER | c.6853+298C>G | FN1 | ENSG00000115414.21 | transcript | ENST00000354785.11 | protein_coding | 41/45 | chr2 | 215369996 | ||||||
chr2:215370086
|
G | C | 1 | a0001c0044t0001g0065 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.6853+208C>G | FN1 | ENSG00000115414.21 | transcript | ENST00000354785.11 | protein_coding | 41/45 | chr2 | 215370086 | ||||||
chr2:215370168
|
G | A | 17 | a0001c0005t0001g0178a0001c0005t0001g0214a0003c0007t0001g0088others(14): Show | 17 | HG02257.hp1 HG02257.hp2 HG02280.hp2 others(14): Show |
intron_variant | MODIFIER | c.6853+126C>T | FN1 | ENSG00000115414.21 | transcript | ENST00000354785.11 | protein_coding | 41/45 | chr2 | 215370168 | ||||||
chr2:215370258
|
G | C | 2 | a0001c0010t0001g0230a0001c0012t0001g0081 | 2 | HG01069.hp2 HG01361.hp1 |
intron_variant | MODIFIER | c.6853+36C>G | FN1 | ENSG00000115414.21 | transcript | ENST00000354785.11 | protein_coding | 41/45 | chr2 | 215370258 | ||||||
chr2:215370265
|
C | T | 6 | a0003c0007t0001g0088a0003c0007t0002g0093a0003c0007t0002g0098others(3): Show | 6 | HG02486.hp1 HG02572.hp1 HG02615.hp1 others(3): Show |
intron_variant | MODIFIER | c.6853+29G>A | FN1 | ENSG00000115414.21 | transcript | ENST00000354785.11 | protein_coding | 41/45 | chr2 | 215370265 | ||||||
chr2:215370282
|
G | C | 1 | a0001c0058t0002g0153 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.6853+12C>G | FN1 | ENSG00000115414.21 | transcript | ENST00000354785.11 | protein_coding | 41/45 | chr2 | 215370282 | ||||||
chr2:215370519
|
T | G | 14 | a0001c0006t0001g0110a0003c0007t0001g0088a0003c0007t0002g0066others(11): Show | 14 | HG02257.hp2 HG02486.hp1 HG02559.hp2 others(11): Show |
intron_variant | MODIFIER | c.6715-87A>C | FN1 | ENSG00000115414.21 | transcript | ENST00000354785.11 | protein_coding | 40/45 | chr2 | 215370519 | ||||||
chr2:215370536
|
A | C | 1 | a0001c0005t0001g0178 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.6715-104T>G | FN1 | ENSG00000115414.21 | transcript | ENST00000354785.11 | protein_coding | 40/45 | chr2 | 215370536 | ||||||
chr2:215370538
|
GACAAAAA | G | 69 | a0001c0002t0001g0126a0001c0002t0001g0134a0001c0002t0001g0138others(66): Show | 70 | HG00280.hp1 HG00323.hp1 HG00609.hp1 others(67): Show |
intron_variant | MODIFIER | c.6715-113_6715-107d others(9): Show |
FN1 | ENSG00000115414.21 | transcript | ENST00000354785.11 | protein_coding | 40/45 | chr2 | 215370538 | ||||||
chr2:215370540
|
C | CAAAAAAA others(3): Show |
1 | a0003c0007t0002g0158 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.6715-109_6715-108i others(12): Show |
FN1 | ENSG00000115414.21 | transcript | ENST00000354785.11 | protein_coding | 40/45 | chr2 | 215370540 | ||||||
chr2:215370540
|
C | CAAAAAAA others(4): Show |
4 | a0001c0005t0001g0178a0003c0007t0002g0066a0003c0007t0002g0156others(1): Show | 4 | HG02257.hp1 HG02886.hp1 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.6715-109_6715-108i others(13): Show |
FN1 | ENSG00000115414.21 | transcript | ENST00000354785.11 | protein_coding | 40/45 | chr2 | 215370540 | ||||||
chr2:215370540
|
C | CAAAAAAA others(5): Show |
6 | a0003c0007t0001g0088a0003c0007t0002g0159a0003c0048t0002g0100others(3): Show | 6 | HG02257.hp2 HG02486.hp1 HG02559.hp2 others(3): Show |
intron_variant | MODIFIER | c.6715-109_6715-108i others(14): Show |
FN1 | ENSG00000115414.21 | transcript | ENST00000354785.11 | protein_coding | 40/45 | chr2 | 215370540 | ||||||
chr2:215370540
|
C | CAAAAAAA others(6): Show |
2 | a0003c0007t0002g0098a0003c0007t0002g0099 | 2 | HG03579.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.6715-109_6715-108i others(15): Show |
FN1 | ENSG00000115414.21 | transcript | ENST00000354785.11 | protein_coding | 40/45 | chr2 | 215370540 | ||||||
chr2:215370540
|
C | CAAAAAAA others(9): Show |
1 | a0003c0007t0002g0093 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.6715-109_6715-108i others(18): Show |
FN1 | ENSG00000115414.21 | transcript | ENST00000354785.11 | protein_coding | 40/45 | chr2 | 215370540 | ||||||
chr2:215370540
|
C | CCAAAAAA others(16): Show |
2 | a0001c0005t0001g0067a0001c0005t0001g0229 | 2 | HG02615.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.6715-109_6715-108i others(25): Show |
FN1 | ENSG00000115414.21 | transcript | ENST00000354785.11 | protein_coding | 40/45 | chr2 | 215370540 | ||||||
chr2:215370541
|
A | C | 2 | a0011c0026t0001g0161a0011c0026t0001g0172 | 2 | HG03209.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.6715-109T>G | FN1 | ENSG00000115414.21 | transcript | ENST00000354785.11 | protein_coding | 40/45 | chr2 | 215370541 | ||||||
chr2:215370547
|
C | A | 19 | a0001c0005t0001g0067a0001c0005t0001g0178a0001c0005t0001g0229others(16): Show | 19 | HG00099.hp1 HG02257.hp1 HG02257.hp2 others(16): Show |
intron_variant | MODIFIER | c.6715-115G>T | FN1 | ENSG00000115414.21 | transcript | ENST00000354785.11 | protein_coding | 40/45 | chr2 | 215370547 | ||||||
chr2:215370554
|
C | A | 94 | a0001c0001t0001g0222a0001c0002t0001g0126a0001c0002t0001g0134others(91): Show | 95 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(92): Show |
intron_variant | MODIFIER | c.6715-122G>T | FN1 | ENSG00000115414.21 | transcript | ENST00000354785.11 | protein_coding | 40/45 | chr2 | 215370554 | ||||||
chr2:215370554
|
C | CA | 5 | a0001c0001t0001g0208a0001c0001t0001g0212a0001c0006t0003g0073others(2): Show | 5 | HG01069.hp1 HG01071.hp2 HG02145.hp2 others(2): Show |
intron_variant | MODIFIER | c.6715-123dupT | FN1 | ENSG00000115414.21 | transcript | ENST00000354785.11 | protein_coding | 40/45 | chr2 | 215370554 | ||||||
chr2:215370595
|
G | A | 1 | a0001c0045t0001g0165 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.6715-163C>T | FN1 | ENSG00000115414.21 | transcript | ENST00000354785.11 | protein_coding | 40/45 | chr2 | 215370595 | ||||||
chr2:215370665
|
A | G | 150 | a0001c0001t0001g0002a0001c0001t0001g0062a0001c0001t0001g0149others(147): Show | 151 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(148): Show |
intron_variant | MODIFIER | c.6715-233T>C | FN1 | ENSG00000115414.21 | transcript | ENST00000354785.11 | protein_coding | 40/45 | chr2 | 215370665 | ||||||
chr2:215370716
|
A | G | 1 | a0001c0012t0001g0154 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.6715-284T>C | FN1 | ENSG00000115414.21 | transcript | ENST00000354785.11 | protein_coding | 40/45 | chr2 | 215370716 | ||||||
chr2:215370731
|
G | A | 4 | a0001c0005t0001g0221a0001c0062t0003g0136a0004c0019t0001g0004others(1): Show | 4 | HG02630.hp2 HG02647.hp1 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.6715-299C>T | FN1 | ENSG00000115414.21 | transcript | ENST00000354785.11 | protein_coding | 40/45 | chr2 | 215370731 | ||||||
chr2:215370799
|
G | A | 1 | a0017c0039t0001g0031 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.6715-367C>T | FN1 | ENSG00000115414.21 | transcript | ENST00000354785.11 | protein_coding | 40/45 | chr2 | 215370799 | ||||||
chr2:215370815
|
G | A | 63 | a0001c0002t0001g0138a0001c0004t0001g0001a0001c0004t0001g0068others(60): Show | 64 | HG00280.hp1 HG00323.hp1 HG00609.hp1 others(61): Show |
intron_variant | MODIFIER | c.6715-383C>T | FN1 | ENSG00000115414.21 | transcript | ENST00000354785.11 | protein_coding | 40/45 | chr2 | 215370815 | ||||||
chr2:215370819
|
A | G | 1 | a0006c0024t0001g0059 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.6715-387T>C | FN1 | ENSG00000115414.21 | transcript | ENST00000354785.11 | protein_coding | 40/45 | chr2 | 215370819 | ||||||
chr2:215371007
|
T | G | 1 | a0001c0006t0004g0003 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.6715-575A>C | FN1 | ENSG00000115414.21 | transcript | ENST00000354785.11 | protein_coding | 40/45 | chr2 | 215371007 | ||||||
chr2:215371015
|
G | A | 2 | a0001c0004t0001g0083a0001c0004t0001g0084 | 2 | HG01168.hp2 HG01169.hp1 |
intron_variant | MODIFIER | c.6715-583C>T | FN1 | ENSG00000115414.21 | transcript | ENST00000354785.11 | protein_coding | 40/45 | chr2 | 215371015 | ||||||
chr2:215371079
|
C | T | 4 | a0002c0003t0001g0013a0002c0003t0001g0016a0002c0008t0001g0033others(1): Show | 4 | HG01070.hp2 HG01071.hp1 HG02683.hp2 others(1): Show |
intron_variant | MODIFIER | c.6715-647G>A | FN1 | ENSG00000115414.21 | transcript | ENST00000354785.11 | protein_coding | 40/45 | chr2 | 215371079 | ||||||
chr2:215371118
|
AT | A | 56 | a0001c0001t0001g0002a0001c0001t0001g0062a0001c0001t0001g0149others(53): Show | 57 | HG00280.hp2 HG00609.hp2 HG00639.hp2 others(54): Show |
intron_variant | MODIFIER | c.6715-687delA | FN1 | ENSG00000115414.21 | transcript | ENST00000354785.11 | protein_coding | 40/45 | chr2 | 215371118 | ||||||
chr2:215371148
|
A | G | 1 | a0017c0039t0001g0031 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.6715-716T>C | FN1 | ENSG00000115414.21 | transcript | ENST00000354785.11 | protein_coding | 40/45 | chr2 | 215371148 | ||||||
chr2:215371192
|
T | C | 8 | a0001c0002t0001g0133a0001c0002t0001g0134a0001c0002t0001g0137others(5): Show | 8 | HG01891.hp2 HG02145.hp1 HG02451.hp2 others(5): Show |
intron_variant | MODIFIER | c.6714+717A>G | FN1 | ENSG00000115414.21 | transcript | ENST00000354785.11 | protein_coding | 40/45 | chr2 | 215371192 | ||||||
chr2:215371247
|
C | A | 1 | a0001c0055t0001g0078 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.6714+662G>T | FN1 | ENSG00000115414.21 | transcript | ENST00000354785.11 | protein_coding | 40/45 | chr2 | 215371247 | ||||||
chr2:215371247
|
C | G | 214 | a0001c0001t0001g0002a0001c0001t0001g0062a0001c0001t0001g0149others(211): Show | 216 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(213): Show |
intron_variant | MODIFIER | c.6714+662G>C | FN1 | ENSG00000115414.21 | transcript | ENST00000354785.11 | protein_coding | 40/45 | chr2 | 215371247 | ||||||
chr2:215371271
|
G | A | 5 | a0001c0002t0001g0113a0001c0005t0001g0214a0001c0006t0004g0003others(2): Show | 5 | HG02280.hp2 HG02723.hp2 HG02895.hp1 others(2): Show |
intron_variant | MODIFIER | c.6714+638C>T | FN1 | ENSG00000115414.21 | transcript | ENST00000354785.11 | protein_coding | 40/45 | chr2 | 215371271 | ||||||
chr2:215371271
|
G | GA | 65 | a0001c0001t0001g0002a0001c0001t0001g0062a0001c0001t0001g0149others(62): Show | 66 | HG00280.hp2 HG00609.hp2 HG00639.hp2 others(63): Show |
intron_variant | MODIFIER | c.6714+637dupT | FN1 | ENSG00000115414.21 | transcript | ENST00000354785.11 | protein_coding | 40/45 | chr2 | 215371271 | ||||||
chr2:215371362
|
G | GT | 5 | a0001c0002t0001g0112a0001c0005t0001g0179a0001c0015t0001g0101others(2): Show | 5 | HG01243.hp1 HG02258.hp1 HG02896.hp2 others(2): Show |
intron_variant | MODIFIER | c.6714+546dupA | FN1 | ENSG00000115414.21 | transcript | ENST00000354785.11 | protein_coding | 40/45 | chr2 | 215371362 | ||||||
chr2:215371468
|
A | ATCTT | 148 | a0001c0002t0001g0111a0001c0002t0001g0112a0001c0002t0001g0113others(145): Show | 149 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(146): Show |
intron_variant | MODIFIER | c.6714+437_6714+440d others(6): Show |
FN1 | ENSG00000115414.21 | transcript | ENST00000354785.11 | protein_coding | 40/45 | chr2 | 215371468 | ||||||
chr2:215371485
|
T | C | 69 | a0001c0002t0001g0126a0001c0002t0001g0138a0001c0004t0001g0001others(66): Show | 70 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(67): Show |
intron_variant | MODIFIER | c.6714+424A>G | FN1 | ENSG00000115414.21 | transcript | ENST00000354785.11 | protein_coding | 40/45 | chr2 | 215371485 | ||||||
chr2:215371554
|
A | G | 1 | a0001c0002t0001g0142 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.6714+355T>C | FN1 | ENSG00000115414.21 | transcript | ENST00000354785.11 | protein_coding | 40/45 | chr2 | 215371554 | ||||||
chr2:215371610
|
T | TA | 8 | a0001c0002t0001g0111a0001c0002t0001g0113a0001c0005t0001g0214others(5): Show | 8 | HG02280.hp1 HG02280.hp2 HG02630.hp2 others(5): Show |
intron_variant | MODIFIER | c.6714+298dupT | FN1 | ENSG00000115414.21 | transcript | ENST00000354785.11 | protein_coding | 40/45 | chr2 | 215371610 | ||||||
chr2:215371610
|
TA | T | 10 | a0001c0002t0001g0123a0001c0002t0001g0133a0001c0002t0001g0134others(7): Show | 10 | HG00323.hp2 HG01891.hp2 HG02145.hp1 others(7): Show |
intron_variant | MODIFIER | c.6714+298delT | FN1 | ENSG00000115414.21 | transcript | ENST00000354785.11 | protein_coding | 40/45 | chr2 | 215371610 | ||||||
chr2:215371673
|
CT | C | 133 | a0001c0001t0001g0002a0001c0001t0001g0062a0001c0001t0001g0149others(130): Show | 134 | HG00140.hp2 HG00280.hp2 HG00609.hp2 others(131): Show |
intron_variant | MODIFIER | c.6714+235delA | FN1 | ENSG00000115414.21 | transcript | ENST00000354785.11 | protein_coding | 40/45 | chr2 | 215371673 | ||||||
chr2:215371673
|
CTT | C | 8 | a0001c0002t0001g0111a0001c0002t0001g0113a0001c0002t0001g0123others(5): Show | 8 | HG00323.hp2 HG02280.hp1 HG02280.hp2 others(5): Show |
intron_variant | MODIFIER | c.6714+234_6714+235d others(4): Show |
FN1 | ENSG00000115414.21 | transcript | ENST00000354785.11 | protein_coding | 40/45 | chr2 | 215371673 | ||||||
chr2:215371673
|
CTTT | C | 69 | a0001c0002t0001g0126a0001c0002t0001g0138a0001c0004t0001g0001others(66): Show | 70 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(67): Show |
intron_variant | MODIFIER | c.6714+233_6714+235d others(5): Show |
FN1 | ENSG00000115414.21 | transcript | ENST00000354785.11 | protein_coding | 40/45 | chr2 | 215371673 | ||||||
chr2:215371688
|
T | C | 8 | a0001c0002t0001g0133a0001c0002t0001g0134a0001c0002t0001g0137others(5): Show | 8 | HG01891.hp2 HG02145.hp1 HG02451.hp2 others(5): Show |
intron_variant | MODIFIER | c.6714+221A>G | FN1 | ENSG00000115414.21 | transcript | ENST00000354785.11 | protein_coding | 40/45 | chr2 | 215371688 | ||||||
chr2:215371759
|
T | C | 9 | a0001c0002t0001g0133a0001c0002t0001g0134a0001c0002t0001g0137others(6): Show | 9 | HG01891.hp2 HG02145.hp1 HG02257.hp2 others(6): Show |
intron_variant | MODIFIER | c.6714+150A>G | FN1 | ENSG00000115414.21 | transcript | ENST00000354785.11 | protein_coding | 40/45 | chr2 | 215371759 | ||||||
chr2:215371809
|
G | A | 58 | a0001c0001t0001g0002a0001c0001t0001g0062a0001c0001t0001g0149others(55): Show | 59 | HG00280.hp2 HG00609.hp2 HG00639.hp2 others(56): Show |
intron_variant | MODIFIER | c.6714+100C>T | FN1 | ENSG00000115414.21 | transcript | ENST00000354785.11 | protein_coding | 40/45 | chr2 | 215371809 | ||||||
chr2:215372696
|
TTC | T | 11 | a0001c0041t0001g0147a0003c0007t0002g0066a0003c0007t0002g0093others(8): Show | 11 | HG02486.hp1 HG02559.hp2 HG02615.hp1 others(8): Show |
intron_variant | MODIFIER | c.6248-323_6248-322d others(4): Show |
FN1 | ENSG00000115414.21 | transcript | ENST00000354785.11 | protein_coding | 39/45 | chr2 | 215372696 | ||||||
chr2:215373206
|
A | T | 64 | a0001c0001t0001g0002a0001c0001t0001g0062a0001c0001t0001g0149others(61): Show | 65 | HG00280.hp2 HG00609.hp2 HG00639.hp2 others(62): Show |
intron_variant | MODIFIER | c.6247+116T>A | FN1 | ENSG00000115414.21 | transcript | ENST00000354785.11 | protein_coding | 39/45 | chr2 | 215373206 | ||||||
chr2:215373290
|
C | T | 2 | a0004c0020t0002g0005a0004c0020t0002g0006 | 2 | HG02970.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.6247+32G>A | FN1 | ENSG00000115414.21 | transcript | ENST00000354785.11 | protein_coding | 39/45 | chr2 | 215373290 | ||||||
chr2:215373445
|
A | G | 1 | a0001c0055t0001g0078 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.6158-34T>C | FN1 | ENSG00000115414.21 | transcript | ENST00000354785.11 | protein_coding | 38/45 | chr2 | 215373445 | ||||||
chr2:215373563
|
A | G | 1 | a0001c0011t0001g0220 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.6158-152T>C | FN1 | ENSG00000115414.21 | transcript | ENST00000354785.11 | protein_coding | 38/45 | chr2 | 215373563 | ||||||
chr2:215373597
|
A | G | 75 | a0001c0001t0001g0002a0001c0001t0001g0062a0001c0001t0001g0149others(72): Show | 76 | HG00280.hp2 HG00609.hp2 HG00639.hp2 others(73): Show |
intron_variant | MODIFIER | c.6158-186T>C | FN1 | ENSG00000115414.21 | transcript | ENST00000354785.11 | protein_coding | 38/45 | chr2 | 215373597 | ||||||
chr2:215373671
|
C | CT | 8 | a0001c0002t0001g0113a0001c0005t0001g0214a0001c0006t0001g0075others(5): Show | 8 | HG00099.hp2 HG00140.hp1 HG02280.hp2 others(5): Show |
intron_variant | MODIFIER | c.6158-261dupA | FN1 | ENSG00000115414.21 | transcript | ENST00000354785.11 | protein_coding | 38/45 | chr2 | 215373671 | ||||||
chr2:215373671
|
CT | C | 25 | a0001c0002t0001g0135a0001c0002t0001g0139a0001c0002t0001g0140others(22): Show | 25 | HG01109.hp2 HG02109.hp1 HG02109.hp2 others(22): Show |
intron_variant | MODIFIER | c.6158-261delA | FN1 | ENSG00000115414.21 | transcript | ENST00000354785.11 | protein_coding | 38/45 | chr2 | 215373671 | ||||||
chr2:215373671
|
CTT | C | 8 | a0001c0044t0001g0065a0002c0014t0001g0053a0003c0056t0002g0097others(5): Show | 8 | HG01255.hp2 HG01361.hp2 HG01975.hp1 others(5): Show |
intron_variant | MODIFIER | c.6158-262_6158-261d others(4): Show |
FN1 | ENSG00000115414.21 | transcript | ENST00000354785.11 | protein_coding | 38/45 | chr2 | 215373671 | ||||||
chr2:215373671
|
CTTTTT | C | 71 | a0001c0001t0001g0002a0001c0001t0001g0062a0001c0001t0001g0149others(68): Show | 72 | HG00280.hp2 HG00609.hp2 HG00639.hp2 others(69): Show |
intron_variant | MODIFIER | c.6158-265_6158-261d others(7): Show |
FN1 | ENSG00000115414.21 | transcript | ENST00000354785.11 | protein_coding | 38/45 | chr2 | 215373671 | ||||||
chr2:215373671
|
CTTTTTTT others(7): Show |
C | 102 | a0001c0002t0001g0111a0001c0002t0001g0114a0001c0002t0001g0119others(99): Show | 103 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(100): Show |
intron_variant | MODIFIER | c.6158-274_6158-261d others(16): Show |
FN1 | ENSG00000115414.21 | transcript | ENST00000354785.11 | protein_coding | 38/45 | chr2 | 215373671 | ||||||
chr2:215373671
|
CTTTTTTT others(8): Show |
C | 3 | a0001c0005t0001g0178a0001c0015t0001g0102a0003c0048t0002g0100 | 3 | HG02257.hp1 HG02572.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.6158-275_6158-261d others(17): Show |
FN1 | ENSG00000115414.21 | transcript | ENST00000354785.11 | protein_coding | 38/45 | chr2 | 215373671 | ||||||
chr2:215373709
|
T | G | 2 | a0004c0020t0002g0005a0004c0020t0002g0006 | 2 | HG02970.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.6158-298A>C | FN1 | ENSG00000115414.21 | transcript | ENST00000354785.11 | protein_coding | 38/45 | chr2 | 215373709 | ||||||
chr2:215373804
|
G | A | 1 | a0001c0006t0004g0003 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.6158-393C>T | FN1 | ENSG00000115414.21 | transcript | ENST00000354785.11 | protein_coding | 38/45 | chr2 | 215373804 | ||||||
chr2:215373884
|
G | A | 77 | a0001c0001t0001g0002a0001c0001t0001g0062a0001c0001t0001g0149others(74): Show | 78 | HG00280.hp2 HG00609.hp2 HG00639.hp2 others(75): Show |
intron_variant | MODIFIER | c.6158-473C>T | FN1 | ENSG00000115414.21 | transcript | ENST00000354785.11 | protein_coding | 38/45 | chr2 | 215373884 | ||||||
chr2:215374247
|
C | CT | 107 | a0001c0002t0001g0111a0001c0002t0001g0114a0001c0002t0001g0119others(104): Show | 108 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(105): Show |
intron_variant | MODIFIER | c.6158-837dupA | FN1 | ENSG00000115414.21 | transcript | ENST00000354785.11 | protein_coding | 38/45 | chr2 | 215374247 | ||||||
chr2:215374252
|
A | G | 2 | a0001c0004t0001g0070a0006c0040t0001g0060 | 2 | HG02451.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.6158-841T>C | FN1 | ENSG00000115414.21 | transcript | ENST00000354785.11 | protein_coding | 38/45 | chr2 | 215374252 | ||||||
chr2:215374383
|
C | T | 1 | a0005c0065t0001g0236 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.6157+831G>A | FN1 | ENSG00000115414.21 | transcript | ENST00000354785.11 | protein_coding | 38/45 | chr2 | 215374383 | ||||||
chr2:215374910
|
G | C | 14 | a0001c0002t0001g0135a0001c0002t0001g0139a0001c0002t0001g0140others(11): Show | 14 | HG01109.hp2 HG01975.hp1 HG02109.hp1 others(11): Show |
intron_variant | MODIFIER | c.6157+304C>G | FN1 | ENSG00000115414.21 | transcript | ENST00000354785.11 | protein_coding | 38/45 | chr2 | 215374910 | ||||||
chr2:215374913
|
T | C | 1 | a0005c0065t0001g0236 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.6157+301A>G | FN1 | ENSG00000115414.21 | transcript | ENST00000354785.11 | protein_coding | 38/45 | chr2 | 215374913 | ||||||
chr2:215375036
|
A | G | 34 | a0001c0002t0001g0111a0001c0002t0001g0114a0001c0002t0001g0119others(31): Show | 34 | HG00140.hp2 HG00323.hp2 HG00642.hp2 others(31): Show |
intron_variant | MODIFIER | c.6157+178T>C | FN1 | ENSG00000115414.21 | transcript | ENST00000354785.11 | protein_coding | 38/45 | chr2 | 215375036 | ||||||
chr2:215375403
|
AAC | A | 77 | a0001c0001t0001g0002a0001c0001t0001g0062a0001c0001t0001g0149others(74): Show | 78 | HG00280.hp2 HG00609.hp2 HG00639.hp2 others(75): Show |
intron_variant | MODIFIER | c.5978-12_5978-11del others(2): Show |
FN1 | ENSG00000115414.21 | transcript | ENST00000354785.11 | protein_coding | 37/45 | chr2 | 215375403 | ||||||
chr2:215375464
|
G | A | 1 | a0001c0058t0002g0153 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.5978-71C>T | FN1 | ENSG00000115414.21 | transcript | ENST00000354785.11 | protein_coding | 37/45 | chr2 | 215375464 | ||||||
chr2:215375549
|
C | T | 1 | a0001c0001t0001g0206 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.5977+80G>A | FN1 | ENSG00000115414.21 | transcript | ENST00000354785.11 | protein_coding | 37/45 | chr2 | 215375549 | ||||||
chr2:215375808
|
A | G | 1 | a0001c0005t0001g0214 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.5888-90T>C | FN1 | ENSG00000115414.21 | transcript | ENST00000354785.11 | protein_coding | 36/45 | chr2 | 215375808 | ||||||
chr2:215375861
|
T | G | 89 | a0001c0001t0001g0002a0001c0001t0001g0062a0001c0001t0001g0149others(86): Show | 90 | HG00280.hp2 HG00609.hp2 HG00639.hp2 others(87): Show |
intron_variant | MODIFIER | c.5888-143A>C | FN1 | ENSG00000115414.21 | transcript | ENST00000354785.11 | protein_coding | 36/45 | chr2 | 215375861 | ||||||
chr2:215375905
|
G | C | 1 | a0002c0003t0001g0047 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.5888-187C>G | FN1 | ENSG00000115414.21 | transcript | ENST00000354785.11 | protein_coding | 36/45 | chr2 | 215375905 | ||||||
chr2:215375913
|
A | T | 1 | a0001c0004t0001g0082 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.5888-195T>A | FN1 | ENSG00000115414.21 | transcript | ENST00000354785.11 | protein_coding | 36/45 | chr2 | 215375913 | ||||||
chr2:215376367
|
G | A | 3 | a0001c0044t0001g0065a0004c0020t0002g0005a0004c0020t0002g0006 | 3 | HG02258.hp2 HG02970.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.5887+131C>T | FN1 | ENSG00000115414.21 | transcript | ENST00000354785.11 | protein_coding | 36/45 | chr2 | 215376367 | ||||||
chr2:215376862
|
A | T | 1 | a0001c0001t0001g0202 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.5711-188T>A | FN1 | ENSG00000115414.21 | transcript | ENST00000354785.11 | protein_coding | 35/45 | chr2 | 215376862 | ||||||
chr2:215376885
|
T | C | 1 | a0001c0001t0001g0183 | 1 | NA19055.hp2 | intron_variant | MODIFIER | c.5711-211A>G | FN1 | ENSG00000115414.21 | transcript | ENST00000354785.11 | protein_coding | 35/45 | chr2 | 215376885 | ||||||
chr2:215377040
|
T | TTG | 3 | a0001c0006t0003g0095a0001c0006t0003g0096a0001c0009t0003g0064 | 3 | HG02895.hp2 HG02897.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.5711-368_5711-367d others(4): Show |
FN1 | ENSG00000115414.21 | transcript | ENST00000354785.11 | protein_coding | 35/45 | chr2 | 215377040 | ||||||
chr2:215377040
|
TTG | T | 211 | a0001c0001t0001g0002a0001c0001t0001g0062a0001c0001t0001g0149others(208): Show | 213 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(210): Show |
intron_variant | MODIFIER | c.5711-368_5711-367d others(4): Show |
FN1 | ENSG00000115414.21 | transcript | ENST00000354785.11 | protein_coding | 35/45 | chr2 | 215377040 | ||||||
chr2:215377040
|
TTGTGTG | T | 4 | a0001c0012t0001g0154a0002c0003t0001g0042a0002c0003t0001g0045others(1): Show | 4 | HG02083.hp2 NA18522.hp1 NA18975.hp1 others(1): Show |
intron_variant | MODIFIER | c.5711-372_5711-367d others(8): Show |
FN1 | ENSG00000115414.21 | transcript | ENST00000354785.11 | protein_coding | 35/45 | chr2 | 215377040 | ||||||
chr2:215377067
|
T | TGA | 14 | a0001c0002t0001g0113a0001c0002t0001g0135a0001c0002t0001g0139others(11): Show | 14 | HG01109.hp2 HG01975.hp1 HG02109.hp1 others(11): Show |
intron_variant | MODIFIER | c.5711-395_5711-394d others(4): Show |
FN1 | ENSG00000115414.21 | transcript | ENST00000354785.11 | protein_coding | 35/45 | chr2 | 215377067 | ||||||
chr2:215377081
|
A | AGAGT | 3 | a0001c0002t0001g0145a0001c0009t0002g0167a0001c0045t0001g0165 | 3 | HG02723.hp2 HG03195.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.5711-408_5711-407i others(6): Show |
FN1 | ENSG00000115414.21 | transcript | ENST00000354785.11 | protein_coding | 35/45 | chr2 | 215377081 | ||||||
chr2:215377081
|
AGT | A | 90 | a0001c0001t0001g0199a0001c0002t0001g0111a0001c0002t0001g0114others(87): Show | 90 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(87): Show |
intron_variant | MODIFIER | c.5711-409_5711-408d others(4): Show |
FN1 | ENSG00000115414.21 | transcript | ENST00000354785.11 | protein_coding | 35/45 | chr2 | 215377081 | ||||||
chr2:215377081
|
AGTGT | A | 57 | a0001c0001t0001g0002a0001c0001t0001g0062a0001c0001t0001g0149others(54): Show | 58 | HG00280.hp2 HG00609.hp2 HG00639.hp2 others(55): Show |
intron_variant | MODIFIER | c.5711-411_5711-408d others(6): Show |
FN1 | ENSG00000115414.21 | transcript | ENST00000354785.11 | protein_coding | 35/45 | chr2 | 215377081 | ||||||
chr2:215377081
|
AGTGTGT | A | 17 | a0001c0002t0001g0112a0001c0002t0001g0133a0001c0002t0001g0134others(14): Show | 17 | HG01243.hp1 HG01891.hp2 HG02145.hp1 others(14): Show |
intron_variant | MODIFIER | c.5711-413_5711-408d others(8): Show |
FN1 | ENSG00000115414.21 | transcript | ENST00000354785.11 | protein_coding | 35/45 | chr2 | 215377081 | ||||||
chr2:215377081
|
AGTGTGTG others(1): Show |
A | 3 | a0001c0046t0001g0164a0004c0019t0001g0004a0004c0019t0001g0007 | 3 | HG02055.hp2 HG02647.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.5711-415_5711-408d others(10): Show |
FN1 | ENSG00000115414.21 | transcript | ENST00000354785.11 | protein_coding | 35/45 | chr2 | 215377081 | ||||||
chr2:215377083
|
T | A | 22 | a0001c0002t0001g0126a0001c0004t0001g0001a0001c0004t0001g0068others(19): Show | 23 | HG00642.hp1 HG00735.hp2 HG00738.hp1 others(20): Show |
intron_variant | MODIFIER | c.5711-409A>T | FN1 | ENSG00000115414.21 | transcript | ENST00000354785.11 | protein_coding | 35/45 | chr2 | 215377083 | ||||||
chr2:215377085
|
T | A | 63 | a0001c0002t0001g0126a0001c0002t0001g0138a0001c0004t0001g0071others(60): Show | 63 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(60): Show |
intron_variant | MODIFIER | c.5711-411A>T | FN1 | ENSG00000115414.21 | transcript | ENST00000354785.11 | protein_coding | 35/45 | chr2 | 215377085 | ||||||
chr2:215377087
|
T | A | 2 | a0002c0003t0001g0032a0002c0003t0001g0037 | 2 | HG01978.hp1 HG02683.hp1 |
intron_variant | MODIFIER | c.5711-413A>T | FN1 | ENSG00000115414.21 | transcript | ENST00000354785.11 | protein_coding | 35/45 | chr2 | 215377087 | ||||||
chr2:215377247
|
A | G | 1 | a0001c0044t0001g0065 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.5711-573T>C | FN1 | ENSG00000115414.21 | transcript | ENST00000354785.11 | protein_coding | 35/45 | chr2 | 215377247 | ||||||
chr2:215377249
|
A | T | 1 | a0001c0012t0001g0154 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.5711-575T>A | FN1 | ENSG00000115414.21 | transcript | ENST00000354785.11 | protein_coding | 35/45 | chr2 | 215377249 | ||||||
chr2:215377467
|
C | G | 3 | a0001c0046t0001g0164a0004c0019t0001g0004a0004c0019t0001g0007 | 3 | HG02055.hp2 HG02647.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.5710+708G>C | FN1 | ENSG00000115414.21 | transcript | ENST00000354785.11 | protein_coding | 35/45 | chr2 | 215377467 | ||||||
chr2:215377468
|
C | G | 4 | a0001c0005t0001g0218a0002c0008t0001g0027a0002c0022t0001g0014others(1): Show | 4 | HG01261.hp2 HG01952.hp1 HG03669.hp2 others(1): Show |
intron_variant | MODIFIER | c.5710+707G>C | FN1 | ENSG00000115414.21 | transcript | ENST00000354785.11 | protein_coding | 35/45 | chr2 | 215377468 | ||||||
chr2:215377469
|
C | A | 4 | a0001c0002t0001g0113a0001c0005t0001g0214a0001c0009t0002g0167others(1): Show | 4 | HG02280.hp2 HG02723.hp2 HG02895.hp1 others(1): Show |
intron_variant | MODIFIER | c.5710+706G>T | FN1 | ENSG00000115414.21 | transcript | ENST00000354785.11 | protein_coding | 35/45 | chr2 | 215377469 | ||||||
chr2:215377581
|
G | A | 1 | a0001c0010t0001g0230 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.5710+594C>T | FN1 | ENSG00000115414.21 | transcript | ENST00000354785.11 | protein_coding | 35/45 | chr2 | 215377581 | ||||||
chr2:215377693
|
C | G | 2 | a0001c0004t0001g0080a0001c0012t0001g0081 | 2 | HG01069.hp2 HG01256.hp1 |
intron_variant | MODIFIER | c.5710+482G>C | FN1 | ENSG00000115414.21 | transcript | ENST00000354785.11 | protein_coding | 35/45 | chr2 | 215377693 | ||||||
chr2:215377727
|
TGG | T | 77 | a0001c0001t0001g0002a0001c0001t0001g0062a0001c0001t0001g0149others(74): Show | 78 | HG00280.hp2 HG00609.hp2 HG00639.hp2 others(75): Show |
intron_variant | MODIFIER | c.5710+446_5710+447d others(4): Show |
FN1 | ENSG00000115414.21 | transcript | ENST00000354785.11 | protein_coding | 35/45 | chr2 | 215377727 | ||||||
chr2:215377892
|
C | G | 1 | a0001c0012t0001g0170 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.5710+283G>C | FN1 | ENSG00000115414.21 | transcript | ENST00000354785.11 | protein_coding | 35/45 | chr2 | 215377892 | ||||||
chr2:215377973
|
A | T | 4 | a0001c0002t0001g0113a0001c0005t0001g0214a0001c0009t0002g0167others(1): Show | 4 | HG02280.hp2 HG02723.hp2 HG02895.hp1 others(1): Show |
intron_variant | MODIFIER | c.5710+202T>A | FN1 | ENSG00000115414.21 | transcript | ENST00000354785.11 | protein_coding | 35/45 | chr2 | 215377973 | ||||||
chr2:215377990
|
T | G | 2 | a0001c0006t0001g0072a0001c0006t0002g0077 | 2 | HG02818.hp2 HG02896.hp1 |
intron_variant | MODIFIER | c.5710+185A>C | FN1 | ENSG00000115414.21 | transcript | ENST00000354785.11 | protein_coding | 35/45 | chr2 | 215377990 | ||||||
chr2:215378096
|
C | A | 1 | a0015c0053t0001g0201 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.5710+79G>T | FN1 | ENSG00000115414.21 | transcript | ENST00000354785.11 | protein_coding | 35/45 | chr2 | 215378096 | ||||||
chr2:215378466
|
C | T | 1 | a0003c0007t0001g0160 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.5623-204G>A | FN1 | ENSG00000115414.21 | transcript | ENST00000354785.11 | protein_coding | 34/45 | chr2 | 215378466 | ||||||
chr2:215378513
|
T | TA | 11 | a0001c0041t0001g0147a0003c0007t0002g0066a0003c0007t0002g0093others(8): Show | 11 | HG02486.hp1 HG02559.hp2 HG02615.hp1 others(8): Show |
intron_variant | MODIFIER | c.5623-252dupT | FN1 | ENSG00000115414.21 | transcript | ENST00000354785.11 | protein_coding | 34/45 | chr2 | 215378513 | ||||||
chr2:215378619
|
A | C | 34 | a0001c0002t0001g0111a0001c0002t0001g0114a0001c0002t0001g0119others(31): Show | 34 | HG00140.hp2 HG00323.hp2 HG00642.hp2 others(31): Show |
intron_variant | MODIFIER | c.5623-357T>G | FN1 | ENSG00000115414.21 | transcript | ENST00000354785.11 | protein_coding | 34/45 | chr2 | 215378619 | ||||||
chr2:215378862
|
T | C | 12 | a0001c0002t0001g0133a0001c0002t0001g0134a0001c0002t0001g0137others(9): Show | 12 | HG01891.hp2 HG02145.hp1 HG02257.hp1 others(9): Show |
intron_variant | MODIFIER | c.5622+268A>G | FN1 | ENSG00000115414.21 | transcript | ENST00000354785.11 | protein_coding | 34/45 | chr2 | 215378862 | ||||||
chr2:215378927
|
A | G | 76 | a0001c0001t0001g0002a0001c0001t0001g0062a0001c0001t0001g0149others(73): Show | 77 | HG00280.hp2 HG00609.hp2 HG00639.hp2 others(74): Show |
intron_variant | MODIFIER | c.5622+203T>C | FN1 | ENSG00000115414.21 | transcript | ENST00000354785.11 | protein_coding | 34/45 | chr2 | 215378927 | ||||||
chr2:215378948
|
T | G | 1 | a0001c0002t0001g0113 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.5622+182A>C | FN1 | ENSG00000115414.21 | transcript | ENST00000354785.11 | protein_coding | 34/45 | chr2 | 215378948 | ||||||
chr2:215379089
|
G | T | 1 | a0002c0008t0001g0008 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.5622+41C>A | FN1 | ENSG00000115414.21 | transcript | ENST00000354785.11 | protein_coding | 34/45 | chr2 | 215379089 | ||||||
chr2:215379109
|
T | C | 217 | a0001c0001t0001g0002a0001c0001t0001g0062a0001c0001t0001g0149others(214): Show | 219 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(216): Show |
intron_variant | MODIFIER | c.5622+21A>G | FN1 | ENSG00000115414.21 | transcript | ENST00000354785.11 | protein_coding | 34/45 | chr2 | 215379109 | ||||||
chr2:215379458
|
AGTAC | A | 174 | a0001c0001t0001g0002a0001c0001t0001g0062a0001c0001t0001g0149others(171): Show | 176 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(173): Show |
intron_variant | MODIFIER | c.5435-145_5435-142d others(6): Show |
FN1 | ENSG00000115414.21 | transcript | ENST00000354785.11 | protein_coding | 33/45 | chr2 | 215379458 | ||||||
chr2:215379680
|
T | G | 1 | a0001c0009t0001g0166 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.5435-363A>C | FN1 | ENSG00000115414.21 | transcript | ENST00000354785.11 | protein_coding | 33/45 | chr2 | 215379680 | ||||||
chr2:215379741
|
G | A | 65 | a0001c0002t0001g0126a0001c0002t0001g0138a0001c0004t0001g0001others(62): Show | 66 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(63): Show |
intron_variant | MODIFIER | c.5435-424C>T | FN1 | ENSG00000115414.21 | transcript | ENST00000354785.11 | protein_coding | 33/45 | chr2 | 215379741 | ||||||
chr2:215379759
|
T | C | 4 | a0001c0002t0001g0113a0001c0005t0001g0214a0001c0009t0002g0167others(1): Show | 4 | HG02280.hp2 HG02723.hp2 HG02895.hp1 others(1): Show |
intron_variant | MODIFIER | c.5435-442A>G | FN1 | ENSG00000115414.21 | transcript | ENST00000354785.11 | protein_coding | 33/45 | chr2 | 215379759 | ||||||
chr2:215380001
|
T | C | 1 | a0001c0010t0001g0152 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.5435-684A>G | FN1 | ENSG00000115414.21 | transcript | ENST00000354785.11 | protein_coding | 33/45 | chr2 | 215380001 | ||||||
chr2:215380045
|
G | A | 1 | a0001c0044t0001g0065 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.5435-728C>T | FN1 | ENSG00000115414.21 | transcript | ENST00000354785.11 | protein_coding | 33/45 | chr2 | 215380045 | ||||||
chr2:215380065
|
G | C | 10 | a0003c0007t0002g0066a0003c0007t0002g0093a0003c0007t0002g0098others(7): Show | 10 | HG02486.hp1 HG02559.hp2 HG02615.hp1 others(7): Show |
intron_variant | MODIFIER | c.5434+746C>G | FN1 | ENSG00000115414.21 | transcript | ENST00000354785.11 | protein_coding | 33/45 | chr2 | 215380065 | ||||||
chr2:215380172
|
A | G | 1 | a0001c0001t0001g0185 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.5434+639T>C | FN1 | ENSG00000115414.21 | transcript | ENST00000354785.11 | protein_coding | 33/45 | chr2 | 215380172 | ||||||
chr2:215380193
|
G | A | 4 | a0001c0002t0001g0113a0001c0005t0001g0214a0001c0009t0002g0167others(1): Show | 4 | HG02280.hp2 HG02723.hp2 HG02895.hp1 others(1): Show |
intron_variant | MODIFIER | c.5434+618C>T | FN1 | ENSG00000115414.21 | transcript | ENST00000354785.11 | protein_coding | 33/45 | chr2 | 215380193 | ||||||
chr2:215380547
|
C | T | 1 | a0002c0013t0001g0010 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.5434+264G>A | FN1 | ENSG00000115414.21 | transcript | ENST00000354785.11 | protein_coding | 33/45 | chr2 | 215380547 | ||||||
chr2:215380597
|
C | G | 1 | a0001c0002t0001g0126 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.5434+214G>C | FN1 | ENSG00000115414.21 | transcript | ENST00000354785.11 | protein_coding | 33/45 | chr2 | 215380597 | ||||||
chr2:215380669
|
C | T | 77 | a0001c0001t0001g0002a0001c0001t0001g0062a0001c0001t0001g0149others(74): Show | 78 | HG00280.hp2 HG00609.hp2 HG00639.hp2 others(75): Show |
intron_variant | MODIFIER | c.5434+142G>A | FN1 | ENSG00000115414.21 | transcript | ENST00000354785.11 | protein_coding | 33/45 | chr2 | 215380669 | ||||||
chr2:215381168
|
A | T | 1 | a0001c0010t0001g0230 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.5165-88T>A | FN1 | ENSG00000115414.21 | transcript | ENST00000354785.11 | protein_coding | 32/45 | chr2 | 215381168 | ||||||
chr2:215381202
|
A | G | 1 | a0001c0042t0001g0148 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.5165-122T>C | FN1 | ENSG00000115414.21 | transcript | ENST00000354785.11 | protein_coding | 32/45 | chr2 | 215381202 | ||||||
chr2:215381357
|
A | G | 65 | a0001c0002t0001g0126a0001c0002t0001g0138a0001c0004t0001g0001others(62): Show | 66 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(63): Show |
intron_variant | MODIFIER | c.5165-277T>C | FN1 | ENSG00000115414.21 | transcript | ENST00000354785.11 | protein_coding | 32/45 | chr2 | 215381357 | ||||||
chr2:215381487
|
T | G | 64 | a0001c0001t0001g0002a0001c0001t0001g0062a0001c0001t0001g0149others(61): Show | 65 | HG00280.hp2 HG00609.hp2 HG00639.hp2 others(62): Show |
intron_variant | MODIFIER | c.5165-407A>C | FN1 | ENSG00000115414.21 | transcript | ENST00000354785.11 | protein_coding | 32/45 | chr2 | 215381487 | ||||||
chr2:215381543
|
G | A | 34 | a0001c0002t0001g0111a0001c0002t0001g0114a0001c0002t0001g0119others(31): Show | 34 | HG00140.hp2 HG00323.hp2 HG00642.hp2 others(31): Show |
intron_variant | MODIFIER | c.5165-463C>T | FN1 | ENSG00000115414.21 | transcript | ENST00000354785.11 | protein_coding | 32/45 | chr2 | 215381543 | ||||||
chr2:215381694
|
G | A | 5 | a0001c0002t0001g0114a0001c0002t0001g0123a0001c0002t0001g0127others(2): Show | 5 | HG00323.hp2 HG00642.hp2 HG00738.hp2 others(2): Show |
intron_variant | MODIFIER | c.5164+518C>T | FN1 | ENSG00000115414.21 | transcript | ENST00000354785.11 | protein_coding | 32/45 | chr2 | 215381694 | ||||||
chr2:215381935
|
T | A | 57 | a0001c0001t0001g0002a0001c0001t0001g0062a0001c0001t0001g0149others(54): Show | 58 | HG00280.hp2 HG00609.hp2 HG00639.hp2 others(55): Show |
intron_variant | MODIFIER | c.5164+277A>T | FN1 | ENSG00000115414.21 | transcript | ENST00000354785.11 | protein_coding | 32/45 | chr2 | 215381935 | ||||||
chr2:215382500
|
C | G | 1 | a0001c0001t0001g0177 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.5051-175G>C | FN1 | ENSG00000115414.21 | transcript | ENST00000354785.11 | protein_coding | 31/45 | chr2 | 215382500 | ||||||
chr2:215382732
|
A | G | 2 | a0002c0008t0001g0021a0002c0008t0001g0041 | 2 | HG01175.hp2 HG03017.hp1 |
intron_variant | MODIFIER | c.5051-407T>C | FN1 | ENSG00000115414.21 | transcript | ENST00000354785.11 | protein_coding | 31/45 | chr2 | 215382732 | ||||||
chr2:215382893
|
T | C | 2 | a0001c0011t0001g0106a0001c0011t0001g0107 | 2 | HG01346.hp1 HG01515.hp2 |
intron_variant | MODIFIER | c.5050+435A>G | FN1 | ENSG00000115414.21 | transcript | ENST00000354785.11 | protein_coding | 31/45 | chr2 | 215382893 | ||||||
chr2:215383159
|
C | G | 10 | a0003c0007t0002g0066a0003c0007t0002g0093a0003c0007t0002g0098others(7): Show | 10 | HG02486.hp1 HG02559.hp2 HG02615.hp1 others(7): Show |
intron_variant | MODIFIER | c.5050+169G>C | FN1 | ENSG00000115414.21 | transcript | ENST00000354785.11 | protein_coding | 31/45 | chr2 | 215383159 | ||||||
chr2:215383582
|
G | T | 192 | a0001c0001t0001g0002a0001c0001t0001g0062a0001c0001t0001g0149others(189): Show | 194 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(191): Show |
intron_variant | MODIFIER | c.4895-99C>A | FN1 | ENSG00000115414.21 | transcript | ENST00000354785.11 | protein_coding | 30/45 | chr2 | 215383582 | ||||||
chr2:215383609
|
G | A | 8 | a0001c0002t0001g0133a0001c0002t0001g0134a0001c0002t0001g0137others(5): Show | 8 | HG01891.hp2 HG02145.hp1 HG02257.hp2 others(5): Show |
intron_variant | MODIFIER | c.4895-126C>T | FN1 | ENSG00000115414.21 | transcript | ENST00000354785.11 | protein_coding | 30/45 | chr2 | 215383609 | ||||||
chr2:215383737
|
A | C | 34 | a0001c0002t0001g0111a0001c0002t0001g0114a0001c0002t0001g0119others(31): Show | 34 | HG00140.hp2 HG00323.hp2 HG00642.hp2 others(31): Show |
intron_variant | MODIFIER | c.4895-254T>G | FN1 | ENSG00000115414.21 | transcript | ENST00000354785.11 | protein_coding | 30/45 | chr2 | 215383737 | ||||||
chr2:215383789
|
C | T | 2 | a0001c0002t0001g0127a0001c0002t0001g0128 | 2 | HG01891.hp1 HG03654.hp1 |
intron_variant | MODIFIER | c.4894+231G>A | FN1 | ENSG00000115414.21 | transcript | ENST00000354785.11 | protein_coding | 30/45 | chr2 | 215383789 | ||||||
chr2:215383799
|
A | T | 16 | a0001c0002t0001g0135a0001c0002t0001g0139a0001c0002t0001g0140others(13): Show | 16 | HG01109.hp2 HG01975.hp1 HG02109.hp1 others(13): Show |
intron_variant | MODIFIER | c.4894+221T>A | FN1 | ENSG00000115414.21 | transcript | ENST00000354785.11 | protein_coding | 30/45 | chr2 | 215383799 | ||||||
chr2:215383805
|
G | A | 3 | a0001c0005t0001g0178a0001c0015t0001g0102a0003c0048t0002g0100 | 3 | HG02257.hp1 HG02572.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.4894+215C>T | FN1 | ENSG00000115414.21 | transcript | ENST00000354785.11 | protein_coding | 30/45 | chr2 | 215383805 | ||||||
chr2:215383840
|
C | T | 16 | a0001c0002t0001g0135a0001c0002t0001g0139a0001c0002t0001g0140others(13): Show | 16 | HG01109.hp2 HG01975.hp1 HG02109.hp1 others(13): Show |
intron_variant | MODIFIER | c.4894+180G>A | FN1 | ENSG00000115414.21 | transcript | ENST00000354785.11 | protein_coding | 30/45 | chr2 | 215383840 | ||||||
chr2:215383883
|
T | C | 75 | a0001c0001t0001g0002a0001c0001t0001g0062a0001c0001t0001g0149others(72): Show | 76 | HG00280.hp2 HG00609.hp2 HG00639.hp2 others(73): Show |
intron_variant | MODIFIER | c.4894+137A>G | FN1 | ENSG00000115414.21 | transcript | ENST00000354785.11 | protein_coding | 30/45 | chr2 | 215383883 | ||||||
chr2:215383984
|
TAA | T | 75 | a0001c0001t0001g0002a0001c0001t0001g0062a0001c0001t0001g0149others(72): Show | 76 | HG00280.hp2 HG00609.hp2 HG00639.hp2 others(73): Show |
intron_variant | MODIFIER | c.4894+34_4894+35del others(2): Show |
FN1 | ENSG00000115414.21 | transcript | ENST00000354785.11 | protein_coding | 30/45 | chr2 | 215383984 | ||||||
chr2:215384313
|
G | A | 1 | a0001c0004t0001g0087 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.4730-129C>T | FN1 | ENSG00000115414.21 | transcript | ENST00000354785.11 | protein_coding | 29/45 | chr2 | 215384313 | ||||||
chr2:215384394
|
C | T | 8 | a0001c0004t0001g0001a0001c0004t0001g0068a0001c0004t0001g0086others(5): Show | 9 | HG00642.hp1 HG00735.hp2 HG01099.hp2 others(6): Show |
intron_variant | MODIFIER | c.4730-210G>A | FN1 | ENSG00000115414.21 | transcript | ENST00000354785.11 | protein_coding | 29/45 | chr2 | 215384394 | ||||||
chr2:215384512
|
CAG | C | 75 | a0001c0001t0001g0002a0001c0001t0001g0062a0001c0001t0001g0149others(72): Show | 76 | HG00280.hp2 HG00609.hp2 HG00639.hp2 others(73): Show |
intron_variant | MODIFIER | c.4730-330_4730-329d others(4): Show |
FN1 | ENSG00000115414.21 | transcript | ENST00000354785.11 | protein_coding | 29/45 | chr2 | 215384512 | ||||||
chr2:215384659
|
G | C | 2 | a0005c0029t0003g0234a0005c0029t0003g0235 | 2 | HG02970.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.4729+201C>G | FN1 | ENSG00000115414.21 | transcript | ENST00000354785.11 | protein_coding | 29/45 | chr2 | 215384659 | ||||||
chr2:215384707
|
T | A | 2 | a0001c0001t0001g0215a0002c0031t0001g0048 | 2 | HG01496.hp1 NA18952.hp1 |
intron_variant | MODIFIER | c.4729+153A>T | FN1 | ENSG00000115414.21 | transcript | ENST00000354785.11 | protein_coding | 29/45 | chr2 | 215384707 | ||||||
chr2:215384747
|
G | A | 1 | a0001c0041t0001g0147 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.4729+113C>T | FN1 | ENSG00000115414.21 | transcript | ENST00000354785.11 | protein_coding | 29/45 | chr2 | 215384747 | ||||||
chr2:215385096
|
C | T | 214 | a0001c0001t0001g0002a0001c0001t0001g0062a0001c0001t0001g0149others(211): Show | 216 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(213): Show |
intron_variant | MODIFIER | c.4613-120G>A | FN1 | ENSG00000115414.21 | transcript | ENST00000354785.11 | protein_coding | 28/45 | chr2 | 215385096 | ||||||
chr2:215385248
|
TA | T | 29 | a0001c0002t0001g0113a0001c0002t0001g0133a0001c0002t0001g0134others(26): Show | 29 | HG01109.hp2 HG01175.hp2 HG01891.hp2 others(26): Show |
intron_variant | MODIFIER | c.4613-273delT | FN1 | ENSG00000115414.21 | transcript | ENST00000354785.11 | protein_coding | 28/45 | chr2 | 215385248 | ||||||
chr2:215385248
|
TAA | T | 95 | a0001c0002t0001g0111a0001c0002t0001g0114a0001c0002t0001g0121others(92): Show | 96 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(93): Show |
intron_variant | MODIFIER | c.4613-274_4613-273d others(4): Show |
FN1 | ENSG00000115414.21 | transcript | ENST00000354785.11 | protein_coding | 28/45 | chr2 | 215385248 | ||||||
chr2:215385248
|
TAAA | T | 5 | a0001c0001t0001g0215a0001c0002t0001g0119a0002c0003t0001g0029others(2): Show | 5 | HG01257.hp1 HG02647.hp1 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.4613-275_4613-273d others(5): Show |
FN1 | ENSG00000115414.21 | transcript | ENST00000354785.11 | protein_coding | 28/45 | chr2 | 215385248 | ||||||
chr2:215385248
|
TAAAA | T | 69 | a0001c0001t0001g0002a0001c0001t0001g0062a0001c0001t0001g0149others(66): Show | 70 | HG00280.hp2 HG00609.hp2 HG00639.hp2 others(67): Show |
intron_variant | MODIFIER | c.4613-276_4613-273d others(6): Show |
FN1 | ENSG00000115414.21 | transcript | ENST00000354785.11 | protein_coding | 28/45 | chr2 | 215385248 | ||||||
chr2:215385283
|
C | T | 9 | a0001c0002t0001g0133a0001c0002t0001g0134a0001c0002t0001g0137others(6): Show | 9 | HG01891.hp2 HG02145.hp1 HG02257.hp2 others(6): Show |
intron_variant | MODIFIER | c.4613-307G>A | FN1 | ENSG00000115414.21 | transcript | ENST00000354785.11 | protein_coding | 28/45 | chr2 | 215385283 | ||||||
chr2:215385287
|
C | T | 9 | a0001c0011t0001g0106a0001c0011t0001g0107a0001c0011t0001g0108others(6): Show | 9 | HG01168.hp1 HG01243.hp2 HG01255.hp2 others(6): Show |
intron_variant | MODIFIER | c.4613-311G>A | FN1 | ENSG00000115414.21 | transcript | ENST00000354785.11 | protein_coding | 28/45 | chr2 | 215385287 | ||||||
chr2:215385328
|
G | A | 74 | a0001c0001t0001g0002a0001c0001t0001g0062a0001c0001t0001g0149others(71): Show | 75 | HG00280.hp2 HG00609.hp2 HG00639.hp2 others(72): Show |
intron_variant | MODIFIER | c.4613-352C>T | FN1 | ENSG00000115414.21 | transcript | ENST00000354785.11 | protein_coding | 28/45 | chr2 | 215385328 | ||||||
chr2:215385526
|
C | G | 1 | a0001c0002t0001g0111 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.4613-550G>C | FN1 | ENSG00000115414.21 | transcript | ENST00000354785.11 | protein_coding | 28/45 | chr2 | 215385526 | ||||||
chr2:215385540
|
C | T | 74 | a0001c0001t0001g0002a0001c0001t0001g0062a0001c0001t0001g0149others(71): Show | 75 | HG00280.hp2 HG00609.hp2 HG00639.hp2 others(72): Show |
intron_variant | MODIFIER | c.4613-564G>A | FN1 | ENSG00000115414.21 | transcript | ENST00000354785.11 | protein_coding | 28/45 | chr2 | 215385540 | ||||||
chr2:215385565
|
A | AAG | 65 | a0001c0002t0001g0126a0001c0002t0001g0138a0001c0004t0001g0001others(62): Show | 66 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(63): Show |
intron_variant | MODIFIER | c.4613-591_4613-590d others(4): Show |
FN1 | ENSG00000115414.21 | transcript | ENST00000354785.11 | protein_coding | 28/45 | chr2 | 215385565 | ||||||
chr2:215385567
|
G | GA | 37 | a0001c0002t0001g0111a0001c0002t0001g0113a0001c0005t0001g0067others(34): Show | 37 | HG01168.hp1 HG01243.hp2 HG01255.hp2 others(34): Show |
intron_variant | MODIFIER | c.4613-592dupT | FN1 | ENSG00000115414.21 | transcript | ENST00000354785.11 | protein_coding | 28/45 | chr2 | 215385567 | ||||||
chr2:215385567
|
G | GAA | 14 | a0001c0002t0001g0135a0001c0002t0001g0139a0001c0002t0001g0140others(11): Show | 14 | HG01109.hp2 HG01975.hp1 HG02109.hp1 others(11): Show |
intron_variant | MODIFIER | c.4613-593_4613-592d others(4): Show |
FN1 | ENSG00000115414.21 | transcript | ENST00000354785.11 | protein_coding | 28/45 | chr2 | 215385567 | ||||||
chr2:215385567
|
GAA | G | 74 | a0001c0001t0001g0002a0001c0001t0001g0062a0001c0001t0001g0149others(71): Show | 75 | HG00280.hp2 HG00609.hp2 HG00639.hp2 others(72): Show |
intron_variant | MODIFIER | c.4613-593_4613-592d others(4): Show |
FN1 | ENSG00000115414.21 | transcript | ENST00000354785.11 | protein_coding | 28/45 | chr2 | 215385567 | ||||||
chr2:215385640
|
C | T | 1 | a0001c0002t0001g0129 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.4613-664G>A | FN1 | ENSG00000115414.21 | transcript | ENST00000354785.11 | protein_coding | 28/45 | chr2 | 215385640 | ||||||
chr2:215385778
|
C | CT | 10 | a0001c0011t0001g0106a0001c0011t0001g0107a0001c0011t0001g0108others(7): Show | 10 | HG01168.hp1 HG01243.hp2 HG01255.hp2 others(7): Show |
intron_variant | MODIFIER | c.4613-803dupA | FN1 | ENSG00000115414.21 | transcript | ENST00000354785.11 | protein_coding | 28/45 | chr2 | 215385778 | ||||||
chr2:215385778
|
CT | C | 119 | a0001c0001t0001g0002a0001c0001t0001g0062a0001c0001t0001g0149others(116): Show | 120 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(117): Show |
intron_variant | MODIFIER | c.4613-803delA | FN1 | ENSG00000115414.21 | transcript | ENST00000354785.11 | protein_coding | 28/45 | chr2 | 215385778 | ||||||
chr2:215385778
|
CTT | C | 76 | a0001c0001t0001g0177a0001c0002t0001g0126a0001c0002t0001g0133others(73): Show | 77 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(74): Show |
intron_variant | MODIFIER | c.4613-804_4613-803d others(4): Show |
FN1 | ENSG00000115414.21 | transcript | ENST00000354785.11 | protein_coding | 28/45 | chr2 | 215385778 | ||||||
chr2:215385779
|
T | C | 1 | a0001c0001t0001g0181 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.4613-803A>G | FN1 | ENSG00000115414.21 | transcript | ENST00000354785.11 | protein_coding | 28/45 | chr2 | 215385779 | ||||||
chr2:215385780
|
T | C | 72 | a0001c0001t0001g0002a0001c0001t0001g0062a0001c0001t0001g0149others(69): Show | 73 | HG00280.hp2 HG00609.hp2 HG00639.hp2 others(70): Show |
intron_variant | MODIFIER | c.4613-804A>G | FN1 | ENSG00000115414.21 | transcript | ENST00000354785.11 | protein_coding | 28/45 | chr2 | 215385780 | ||||||
chr2:215385781
|
T | C | 1 | a0001c0001t0001g0177 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.4613-805A>G | FN1 | ENSG00000115414.21 | transcript | ENST00000354785.11 | protein_coding | 28/45 | chr2 | 215385781 | ||||||
chr2:215385960
|
T | G | 6 | a0001c0002t0001g0112a0001c0005t0001g0179a0001c0015t0001g0101others(3): Show | 6 | HG01243.hp1 HG02258.hp1 HG02896.hp2 others(3): Show |
intron_variant | MODIFIER | c.4612+729A>C | FN1 | ENSG00000115414.21 | transcript | ENST00000354785.11 | protein_coding | 28/45 | chr2 | 215385960 | ||||||
chr2:215385998
|
G | A | 4 | a0001c0002t0001g0113a0001c0005t0001g0214a0001c0009t0002g0167others(1): Show | 4 | HG02280.hp2 HG02723.hp2 HG02895.hp1 others(1): Show |
intron_variant | MODIFIER | c.4612+691C>T | FN1 | ENSG00000115414.21 | transcript | ENST00000354785.11 | protein_coding | 28/45 | chr2 | 215385998 | ||||||
chr2:215386022
|
C | T | 64 | a0001c0001t0001g0002a0001c0001t0001g0062a0001c0001t0001g0149others(61): Show | 65 | HG00280.hp2 HG00609.hp2 HG00639.hp2 others(62): Show |
intron_variant | MODIFIER | c.4612+667G>A | FN1 | ENSG00000115414.21 | transcript | ENST00000354785.11 | protein_coding | 28/45 | chr2 | 215386022 | ||||||
chr2:215386023
|
G | A | 8 | a0001c0002t0001g0133a0001c0002t0001g0134a0001c0002t0001g0137others(5): Show | 8 | HG01891.hp2 HG02145.hp1 HG02257.hp2 others(5): Show |
intron_variant | MODIFIER | c.4612+666C>T | FN1 | ENSG00000115414.21 | transcript | ENST00000354785.11 | protein_coding | 28/45 | chr2 | 215386023 | ||||||
chr2:215386076
|
C | CT | 20 | a0001c0002t0001g0126a0001c0002t0001g0130a0001c0002t0001g0141others(17): Show | 20 | HG00735.hp2 HG00738.hp1 HG00738.hp2 others(17): Show |
intron_variant | MODIFIER | c.4612+612dupA | FN1 | ENSG00000115414.21 | transcript | ENST00000354785.11 | protein_coding | 28/45 | chr2 | 215386076 | ||||||
chr2:215386076
|
C | CTTTTTT | 41 | a0001c0001t0001g0062a0001c0001t0001g0150a0001c0001t0001g0169others(38): Show | 41 | HG00280.hp2 HG00609.hp2 HG00639.hp2 others(38): Show |
intron_variant | MODIFIER | c.4612+607_4612+612d others(8): Show |
FN1 | ENSG00000115414.21 | transcript | ENST00000354785.11 | protein_coding | 28/45 | chr2 | 215386076 | ||||||
chr2:215386076
|
C | CTTTTTTT | 27 | a0001c0001t0001g0149a0001c0001t0001g0151a0001c0001t0001g0175others(24): Show | 27 | HG00735.hp1 HG01071.hp2 HG01109.hp1 others(24): Show |
intron_variant | MODIFIER | c.4612+606_4612+612d others(9): Show |
FN1 | ENSG00000115414.21 | transcript | ENST00000354785.11 | protein_coding | 28/45 | chr2 | 215386076 | ||||||
chr2:215386076
|
CT | C | 15 | a0001c0002t0001g0135a0001c0002t0001g0140a0001c0002t0001g0142others(12): Show | 15 | HG01109.hp2 HG01975.hp1 HG02055.hp1 others(12): Show |
intron_variant | MODIFIER | c.4612+612delA | FN1 | ENSG00000115414.21 | transcript | ENST00000354785.11 | protein_coding | 28/45 | chr2 | 215386076 | ||||||
chr2:215386123
|
G | C | 1 | a0001c0001t0001g0197 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.4612+566C>G | FN1 | ENSG00000115414.21 | transcript | ENST00000354785.11 | protein_coding | 28/45 | chr2 | 215386123 | ||||||
chr2:215386164
|
G | A | 30 | a0001c0002t0001g0111a0001c0002t0001g0114a0001c0002t0001g0119others(27): Show | 30 | HG00140.hp2 HG00323.hp2 HG00642.hp2 others(27): Show |
intron_variant | MODIFIER | c.4612+525C>T | FN1 | ENSG00000115414.21 | transcript | ENST00000354785.11 | protein_coding | 28/45 | chr2 | 215386164 | ||||||
chr2:215386548
|
A | G | 1 | a0001c0012t0001g0079 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.4612+141T>C | FN1 | ENSG00000115414.21 | transcript | ENST00000354785.11 | protein_coding | 28/45 | chr2 | 215386548 | ||||||
chr2:215386556
|
T | C | 1 | a0001c0001t0001g0209 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.4612+133A>G | FN1 | ENSG00000115414.21 | transcript | ENST00000354785.11 | protein_coding | 28/45 | chr2 | 215386556 | ||||||
chr2:215386558
|
A | T | 2 | a0001c0002t0001g0111a0001c0005t0001g0221 | 2 | HG02280.hp1 HG02630.hp2 |
intron_variant | MODIFIER | c.4612+131T>A | FN1 | ENSG00000115414.21 | transcript | ENST00000354785.11 | protein_coding | 28/45 | chr2 | 215386558 | ||||||
chr2:215386568
|
A | AT | 5 | a0001c0006t0001g0090a0001c0006t0001g0091a0001c0006t0003g0095others(2): Show | 5 | HG01256.hp2 HG01258.hp1 HG02895.hp2 others(2): Show |
intron_variant | MODIFIER | c.4612+120dupA | FN1 | ENSG00000115414.21 | transcript | ENST00000354785.11 | protein_coding | 28/45 | chr2 | 215386568 | ||||||
chr2:215386568
|
AT | A | 88 | a0001c0001t0001g0002a0001c0001t0001g0149a0001c0001t0001g0150others(85): Show | 89 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(86): Show |
intron_variant | MODIFIER | c.4612+120delA | FN1 | ENSG00000115414.21 | transcript | ENST00000354785.11 | protein_coding | 28/45 | chr2 | 215386568 | ||||||
chr2:215386568
|
ATT | A | 54 | a0001c0001t0001g0062a0001c0001t0001g0171a0001c0001t0001g0188others(51): Show | 55 | HG00099.hp1 HG00642.hp1 HG00735.hp2 others(52): Show |
intron_variant | MODIFIER | c.4612+119_4612+120d others(4): Show |
FN1 | ENSG00000115414.21 | transcript | ENST00000354785.11 | protein_coding | 28/45 | chr2 | 215386568 | ||||||
chr2:215386568
|
ATTT | A | 42 | a0001c0002t0001g0126a0001c0002t0001g0137a0001c0002t0001g0139others(39): Show | 42 | HG00280.hp1 HG00323.hp1 HG00609.hp1 others(39): Show |
intron_variant | MODIFIER | c.4612+118_4612+120d others(5): Show |
FN1 | ENSG00000115414.21 | transcript | ENST00000354785.11 | protein_coding | 28/45 | chr2 | 215386568 | ||||||
chr2:215386568
|
ATTTTTTT | A | 6 | a0001c0011t0001g0106a0001c0011t0001g0107a0001c0011t0001g0108others(3): Show | 6 | HG01168.hp1 HG01243.hp2 HG01346.hp1 others(3): Show |
intron_variant | MODIFIER | c.4612+114_4612+120d others(9): Show |
FN1 | ENSG00000115414.21 | transcript | ENST00000354785.11 | protein_coding | 28/45 | chr2 | 215386568 | ||||||
chr2:215386602
|
G | T | 3 | a0001c0005t0001g0178a0001c0015t0001g0102a0003c0048t0002g0100 | 3 | HG02257.hp1 HG02572.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.4612+87C>A | FN1 | ENSG00000115414.21 | transcript | ENST00000354785.11 | protein_coding | 28/45 | chr2 | 215386602 | ||||||
chr2:215386974
|
G | A | 74 | a0001c0001t0001g0002a0001c0001t0001g0062a0001c0001t0001g0149others(71): Show | 75 | HG00280.hp2 HG00609.hp2 HG00639.hp2 others(72): Show |
intron_variant | MODIFIER | c.4343-16C>T | FN1 | ENSG00000115414.21 | transcript | ENST00000354785.11 | protein_coding | 27/45 | chr2 | 215386974 | ||||||
chr2:215387161
|
T | C | 1 | a0017c0039t0001g0031 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.4343-203A>G | FN1 | ENSG00000115414.21 | transcript | ENST00000354785.11 | protein_coding | 27/45 | chr2 | 215387161 | ||||||
chr2:215387370
|
ACT | A | 75 | a0001c0001t0001g0002a0001c0001t0001g0062a0001c0001t0001g0149others(72): Show | 76 | HG00280.hp2 HG00609.hp2 HG00639.hp2 others(73): Show |
intron_variant | MODIFIER | c.4343-414_4343-413d others(4): Show |
FN1 | ENSG00000115414.21 | transcript | ENST00000354785.11 | protein_coding | 27/45 | chr2 | 215387370 | ||||||
chr2:215387577
|
T | C | 34 | a0001c0002t0001g0111a0001c0002t0001g0114a0001c0002t0001g0119others(31): Show | 34 | HG00140.hp2 HG00323.hp2 HG00642.hp2 others(31): Show |
intron_variant | MODIFIER | c.4343-619A>G | FN1 | ENSG00000115414.21 | transcript | ENST00000354785.11 | protein_coding | 27/45 | chr2 | 215387577 | ||||||
chr2:215387599
|
T | C | 1 | a0001c0015t0001g0102 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.4342+613A>G | FN1 | ENSG00000115414.21 | transcript | ENST00000354785.11 | protein_coding | 27/45 | chr2 | 215387599 | ||||||
chr2:215387736
|
C | T | 1 | a0005c0065t0001g0236 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.4342+476G>A | FN1 | ENSG00000115414.21 | transcript | ENST00000354785.11 | protein_coding | 27/45 | chr2 | 215387736 | ||||||
chr2:215388033
|
T | C | 79 | a0001c0001t0001g0002a0001c0001t0001g0062a0001c0001t0001g0149others(76): Show | 80 | HG00280.hp2 HG00609.hp2 HG00639.hp2 others(77): Show |
intron_variant | MODIFIER | c.4342+179A>G | FN1 | ENSG00000115414.21 | transcript | ENST00000354785.11 | protein_coding | 27/45 | chr2 | 215388033 | ||||||
chr2:215388316
|
G | C | 96 | a0001c0002t0001g0111a0001c0002t0001g0114a0001c0002t0001g0119others(93): Show | 97 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(94): Show |
intron_variant | MODIFIER | c.4253-15C>G | FN1 | ENSG00000115414.21 | transcript | ENST00000354785.11 | protein_coding | 26/45 | chr2 | 215388316 | ||||||
chr2:215388606
|
C | T | 1 | a0001c0041t0001g0147 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.4253-305G>A | FN1 | ENSG00000115414.21 | transcript | ENST00000354785.11 | protein_coding | 26/45 | chr2 | 215388606 | ||||||
chr2:215388731
|
C | T | 106 | a0001c0002t0001g0111a0001c0002t0001g0114a0001c0002t0001g0119others(103): Show | 107 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(104): Show |
intron_variant | MODIFIER | c.4253-430G>A | FN1 | ENSG00000115414.21 | transcript | ENST00000354785.11 | protein_coding | 26/45 | chr2 | 215388731 | ||||||
chr2:215388771
|
G | A | 1 | a0001c0006t0004g0003 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.4253-470C>T | FN1 | ENSG00000115414.21 | transcript | ENST00000354785.11 | protein_coding | 26/45 | chr2 | 215388771 | ||||||
chr2:215388903
|
A | T | 9 | a0001c0002t0001g0133a0001c0002t0001g0134a0001c0002t0001g0137others(6): Show | 9 | HG01891.hp2 HG02145.hp1 HG02257.hp2 others(6): Show |
intron_variant | MODIFIER | c.4253-602T>A | FN1 | ENSG00000115414.21 | transcript | ENST00000354785.11 | protein_coding | 26/45 | chr2 | 215388903 | ||||||
chr2:215388957
|
C | G | 17 | a0001c0002t0001g0135a0001c0002t0001g0139a0001c0002t0001g0140others(14): Show | 17 | HG01109.hp2 HG01975.hp1 HG02109.hp1 others(14): Show |
intron_variant | MODIFIER | c.4253-656G>C | FN1 | ENSG00000115414.21 | transcript | ENST00000354785.11 | protein_coding | 26/45 | chr2 | 215388957 | ||||||
chr2:215389037
|
TGA | T | 64 | a0001c0002t0001g0126a0001c0002t0001g0138a0001c0004t0001g0001others(61): Show | 65 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(62): Show |
intron_variant | MODIFIER | c.4253-738_4253-737d others(4): Show |
FN1 | ENSG00000115414.21 | transcript | ENST00000354785.11 | protein_coding | 26/45 | chr2 | 215389037 | ||||||
chr2:215389309
|
A | G | 111 | a0001c0002t0001g0111a0001c0002t0001g0114a0001c0002t0001g0119others(108): Show | 112 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(109): Show |
intron_variant | MODIFIER | c.4253-1008T>C | FN1 | ENSG00000115414.21 | transcript | ENST00000354785.11 | protein_coding | 26/45 | chr2 | 215389309 | ||||||
chr2:215389350
|
G | A | 1 | a0001c0015t0001g0104 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.4253-1049C>T | FN1 | ENSG00000115414.21 | transcript | ENST00000354785.11 | protein_coding | 26/45 | chr2 | 215389350 | ||||||
chr2:215389362
|
C | CAAGG | 4 | a0001c0064t0001g0117a0008c0018t0001g0115a0008c0018t0001g0116others(1): Show | 4 | HG01255.hp2 HG01261.hp1 HG01361.hp2 others(1): Show |
intron_variant | MODIFIER | c.4253-1062_4253-106 others(8): Show |
FN1 | ENSG00000115414.21 | transcript | ENST00000354785.11 | protein_coding | 26/45 | chr2 | 215389362 | ||||||
chr2:215389403
|
T | G | 1 | a0001c0001t0001g0149 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.4253-1102A>C | FN1 | ENSG00000115414.21 | transcript | ENST00000354785.11 | protein_coding | 26/45 | chr2 | 215389403 | ||||||
chr2:215389422
|
ACAGT | A | 11 | a0001c0015t0001g0102a0003c0007t0002g0066a0003c0007t0002g0093others(8): Show | 11 | HG02486.hp1 HG02559.hp2 HG02615.hp1 others(8): Show |
intron_variant | MODIFIER | c.4253-1125_4253-112 others(8): Show |
FN1 | ENSG00000115414.21 | transcript | ENST00000354785.11 | protein_coding | 26/45 | chr2 | 215389422 | ||||||
chr2:215389569
|
C | T | 2 | a0001c0005t0001g0190a0001c0005t0001g0191 | 2 | HG02300.hp2 NA18975.hp2 |
intron_variant | MODIFIER | c.4253-1268G>A | FN1 | ENSG00000115414.21 | transcript | ENST00000354785.11 | protein_coding | 26/45 | chr2 | 215389569 | ||||||
chr2:215389651
|
G | A | 3 | a0001c0002t0001g0126a0001c0010t0001g0184a0016c0043t0001g0168 | 3 | HG00738.hp1 HG01934.hp1 NA18952.hp2 |
intron_variant | MODIFIER | c.4253-1350C>T | FN1 | ENSG00000115414.21 | transcript | ENST00000354785.11 | protein_coding | 26/45 | chr2 | 215389651 | ||||||
chr2:215389658
|
C | T | 1 | a0004c0019t0001g0007 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.4253-1357G>A | FN1 | ENSG00000115414.21 | transcript | ENST00000354785.11 | protein_coding | 26/45 | chr2 | 215389658 | ||||||
chr2:215389745
|
G | A | 3 | a0001c0001t0001g0171a0001c0001t0001g0188a0001c0001t0001g0189 | 3 | HG03491.hp1 HG03831.hp1 HG03942.hp1 |
intron_variant | MODIFIER | c.4253-1444C>T | FN1 | ENSG00000115414.21 | transcript | ENST00000354785.11 | protein_coding | 26/45 | chr2 | 215389745 | ||||||
chr2:215389777
|
G | A | 6 | a0001c0005t0001g0067a0001c0005t0001g0229a0002c0014t0001g0052others(3): Show | 6 | HG01884.hp2 HG02615.hp2 HG02717.hp2 others(3): Show |
intron_variant | MODIFIER | c.4253-1476C>T | FN1 | ENSG00000115414.21 | transcript | ENST00000354785.11 | protein_coding | 26/45 | chr2 | 215389777 | ||||||
chr2:215389790
|
AAAAACAA others(3): Show |
A | 100 | a0001c0001t0001g0002a0001c0001t0001g0062a0001c0001t0001g0149others(97): Show | 101 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(98): Show |
intron_variant | MODIFIER | c.4253-1499_4253-149 others(14): Show |
FN1 | ENSG00000115414.21 | transcript | ENST00000354785.11 | protein_coding | 26/45 | chr2 | 215389790 | ||||||
chr2:215389833
|
G | A | 12 | a0001c0002t0001g0135a0001c0002t0001g0139a0001c0002t0001g0140others(9): Show | 12 | HG01109.hp2 HG01975.hp1 HG02109.hp1 others(9): Show |
intron_variant | MODIFIER | c.4253-1532C>T | FN1 | ENSG00000115414.21 | transcript | ENST00000354785.11 | protein_coding | 26/45 | chr2 | 215389833 | ||||||
chr2:215389839
|
T | A | 205 | a0001c0001t0001g0002a0001c0001t0001g0062a0001c0001t0001g0149others(202): Show | 207 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(204): Show |
intron_variant | MODIFIER | c.4253-1538A>T | FN1 | ENSG00000115414.21 | transcript | ENST00000354785.11 | protein_coding | 26/45 | chr2 | 215389839 | ||||||
chr2:215389853
|
C | G | 3 | a0001c0001t0001g0062a0001c0001t0001g0210a0001c0001t0001g0216 | 3 | HG00280.hp2 HG00735.hp1 HG01515.hp1 |
intron_variant | MODIFIER | c.4253-1552G>C | FN1 | ENSG00000115414.21 | transcript | ENST00000354785.11 | protein_coding | 26/45 | chr2 | 215389853 | ||||||
chr2:215389971
|
C | A | 12 | a0001c0009t0001g0157a0001c0015t0001g0102a0003c0007t0002g0066others(9): Show | 12 | HG02486.hp1 HG02559.hp2 HG02615.hp1 others(9): Show |
intron_variant | MODIFIER | c.4252+1661G>T | FN1 | ENSG00000115414.21 | transcript | ENST00000354785.11 | protein_coding | 26/45 | chr2 | 215389971 | ||||||
chr2:215390170
|
G | A | 3 | a0001c0005t0001g0214a0001c0009t0002g0167a0001c0045t0001g0165 | 3 | HG02280.hp2 HG02723.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.4252+1462C>T | FN1 | ENSG00000115414.21 | transcript | ENST00000354785.11 | protein_coding | 26/45 | chr2 | 215390170 | ||||||
chr2:215390182
|
ATTTG | A | 12 | a0001c0009t0001g0157a0001c0015t0001g0102a0003c0007t0002g0066others(9): Show | 12 | HG02486.hp1 HG02559.hp2 HG02615.hp1 others(9): Show |
intron_variant | MODIFIER | c.4252+1446_4252+144 others(8): Show |
FN1 | ENSG00000115414.21 | transcript | ENST00000354785.11 | protein_coding | 26/45 | chr2 | 215390182 | ||||||
chr2:215390206
|
C | T | 1 | a0001c0004t0001g0070 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.4252+1426G>A | FN1 | ENSG00000115414.21 | transcript | ENST00000354785.11 | protein_coding | 26/45 | chr2 | 215390206 | ||||||
chr2:215390316
|
C | T | 1 | a0001c0004t0001g0231 | 1 | HG03492.hp2 | intron_variant | MODIFIER | c.4252+1316G>A | FN1 | ENSG00000115414.21 | transcript | ENST00000354785.11 | protein_coding | 26/45 | chr2 | 215390316 | ||||||
chr2:215390343
|
C | T | 4 | a0002c0003t0001g0013a0002c0003t0001g0016a0002c0008t0001g0033others(1): Show | 4 | HG01070.hp2 HG01071.hp1 HG02683.hp2 others(1): Show |
intron_variant | MODIFIER | c.4252+1289G>A | FN1 | ENSG00000115414.21 | transcript | ENST00000354785.11 | protein_coding | 26/45 | chr2 | 215390343 | ||||||
chr2:215390353
|
T | A | 1 | a0001c0012t0001g0154 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.4252+1279A>T | FN1 | ENSG00000115414.21 | transcript | ENST00000354785.11 | protein_coding | 26/45 | chr2 | 215390353 | ||||||
chr2:215390470
|
A | C | 2 | a0004c0019t0001g0004a0004c0019t0001g0007 | 2 | HG02647.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.4252+1162T>G | FN1 | ENSG00000115414.21 | transcript | ENST00000354785.11 | protein_coding | 26/45 | chr2 | 215390470 | ||||||
chr2:215390531
|
G | C | 3 | a0001c0005t0001g0214a0001c0009t0002g0167a0001c0045t0001g0165 | 3 | HG02280.hp2 HG02723.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.4252+1101C>G | FN1 | ENSG00000115414.21 | transcript | ENST00000354785.11 | protein_coding | 26/45 | chr2 | 215390531 | ||||||
chr2:215390542
|
C | T | 213 | a0001c0001t0001g0002a0001c0001t0001g0062a0001c0001t0001g0149others(210): Show | 215 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(212): Show |
intron_variant | MODIFIER | c.4252+1090G>A | FN1 | ENSG00000115414.21 | transcript | ENST00000354785.11 | protein_coding | 26/45 | chr2 | 215390542 | ||||||
chr2:215390595
|
G | A | 237 | a0001c0001t0001g0002a0001c0001t0001g0062a0001c0001t0001g0149others(234): Show | 239 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(236): Show |
intron_variant | MODIFIER | c.4252+1037C>T | FN1 | ENSG00000115414.21 | transcript | ENST00000354785.11 | protein_coding | 26/45 | chr2 | 215390595 | ||||||
chr2:215390681
|
TGCTCTA | T | 64 | a0001c0001t0001g0217a0001c0002t0001g0126a0001c0002t0001g0138others(61): Show | 65 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(62): Show |
intron_variant | MODIFIER | c.4252+945_4252+950d others(8): Show |
FN1 | ENSG00000115414.21 | transcript | ENST00000354785.11 | protein_coding | 26/45 | chr2 | 215390681 | ||||||
chr2:215390803
|
T | C | 17 | a0001c0004t0001g0001a0001c0004t0001g0068a0001c0004t0001g0080others(14): Show | 18 | HG00099.hp1 HG00323.hp1 HG00642.hp1 others(15): Show |
intron_variant | MODIFIER | c.4252+829A>G | FN1 | ENSG00000115414.21 | transcript | ENST00000354785.11 | protein_coding | 26/45 | chr2 | 215390803 | ||||||
chr2:215390919
|
C | T | 2 | a0001c0002t0001g0232a0001c0002t0001g0233 | 2 | HG03491.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.4252+713G>A | FN1 | ENSG00000115414.21 | transcript | ENST00000354785.11 | protein_coding | 26/45 | chr2 | 215390919 | ||||||
chr2:215391075
|
G | T | 1 | a0001c0012t0001g0089 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.4252+557C>A | FN1 | ENSG00000115414.21 | transcript | ENST00000354785.11 | protein_coding | 26/45 | chr2 | 215391075 | ||||||
chr2:215391167
|
A | T | 1 | a0001c0001t0001g0222 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.4252+465T>A | FN1 | ENSG00000115414.21 | transcript | ENST00000354785.11 | protein_coding | 26/45 | chr2 | 215391167 | ||||||
chr2:215391194
|
AC | A | 6 | a0001c0011t0001g0106a0001c0011t0001g0107a0001c0011t0001g0108others(3): Show | 6 | HG01168.hp1 HG01243.hp2 HG01346.hp1 others(3): Show |
intron_variant | MODIFIER | c.4252+437delG | FN1 | ENSG00000115414.21 | transcript | ENST00000354785.11 | protein_coding | 26/45 | chr2 | 215391194 | ||||||
chr2:215391269
|
T | C | 10 | a0001c0002t0001g0113a0001c0005t0001g0214a0001c0009t0002g0167others(7): Show | 10 | HG02258.hp2 HG02280.hp2 HG02647.hp1 others(7): Show |
intron_variant | MODIFIER | c.4252+363A>G | FN1 | ENSG00000115414.21 | transcript | ENST00000354785.11 | protein_coding | 26/45 | chr2 | 215391269 | ||||||
chr2:215391428
|
T | A | 66 | a0001c0001t0001g0217a0001c0002t0001g0126a0001c0002t0001g0138others(63): Show | 67 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(64): Show |
intron_variant | MODIFIER | c.4252+204A>T | FN1 | ENSG00000115414.21 | transcript | ENST00000354785.11 | protein_coding | 26/45 | chr2 | 215391428 | ||||||
chr2:215391498
|
T | G | 78 | a0001c0001t0001g0217a0001c0002t0001g0126a0001c0002t0001g0135others(75): Show | 79 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(76): Show |
intron_variant | MODIFIER | c.4252+134A>C | FN1 | ENSG00000115414.21 | transcript | ENST00000354785.11 | protein_coding | 26/45 | chr2 | 215391498 | ||||||
chr2:215391504
|
G | C | 66 | a0001c0001t0001g0217a0001c0002t0001g0126a0001c0002t0001g0138others(63): Show | 67 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(64): Show |
intron_variant | MODIFIER | c.4252+128C>G | FN1 | ENSG00000115414.21 | transcript | ENST00000354785.11 | protein_coding | 26/45 | chr2 | 215391504 | ||||||
chr2:215391520
|
T | G | 1 | a0002c0003t0001g0026 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.4252+112A>C | FN1 | ENSG00000115414.21 | transcript | ENST00000354785.11 | protein_coding | 26/45 | chr2 | 215391520 | ||||||
chr2:215391621
|
C | G | 2 | a0002c0003t0001g0039a0002c0003t0001g0040 | 2 | HG00741.hp2 HG01167.hp2 |
intron_variant | MODIFIER | c.4252+11G>C | FN1 | ENSG00000115414.21 | transcript | ENST00000354785.11 | protein_coding | 26/45 | chr2 | 215391621 | ||||||
chr2:215391892
|
T | C | 161 | a0001c0001t0001g0002a0001c0001t0001g0062a0001c0001t0001g0149others(158): Show | 162 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(159): Show |
intron_variant | MODIFIER | c.4070-78A>G | FN1 | ENSG00000115414.21 | transcript | ENST00000354785.11 | protein_coding | 25/45 | chr2 | 215391892 | ||||||
chr2:215391984
|
T | C | 161 | a0001c0001t0001g0002a0001c0001t0001g0062a0001c0001t0001g0149others(158): Show | 162 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(159): Show |
intron_variant | MODIFIER | c.4070-170A>G | FN1 | ENSG00000115414.21 | transcript | ENST00000354785.11 | protein_coding | 25/45 | chr2 | 215391984 | ||||||
chr2:215392052
|
A | G | 77 | a0001c0001t0001g0217a0001c0002t0001g0126a0001c0002t0001g0138others(74): Show | 78 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(75): Show |
intron_variant | MODIFIER | c.4070-238T>C | FN1 | ENSG00000115414.21 | transcript | ENST00000354785.11 | protein_coding | 25/45 | chr2 | 215392052 | ||||||
chr2:215392258
|
T | C | 31 | a0001c0002t0001g0113a0001c0002t0001g0135a0001c0002t0001g0139others(28): Show | 31 | HG01109.hp2 HG01168.hp1 HG01243.hp2 others(28): Show |
intron_variant | MODIFIER | c.4070-444A>G | FN1 | ENSG00000115414.21 | transcript | ENST00000354785.11 | protein_coding | 25/45 | chr2 | 215392258 | ||||||
chr2:215392542
|
T | G | 223 | a0001c0001t0001g0002a0001c0001t0001g0062a0001c0001t0001g0149others(220): Show | 225 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(222): Show |
intron_variant | MODIFIER | c.4069+389A>C | FN1 | ENSG00000115414.21 | transcript | ENST00000354785.11 | protein_coding | 25/45 | chr2 | 215392542 | ||||||
chr2:215392624
|
C | A | 177 | a0001c0001t0001g0002a0001c0001t0001g0062a0001c0001t0001g0149others(174): Show | 179 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(176): Show |
intron_variant | MODIFIER | c.4069+307G>T | FN1 | ENSG00000115414.21 | transcript | ENST00000354785.11 | protein_coding | 25/45 | chr2 | 215392624 | ||||||
chr2:215392678
|
G | A | 1 | a0001c0046t0001g0164 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.4069+253C>T | FN1 | ENSG00000115414.21 | transcript | ENST00000354785.11 | protein_coding | 25/45 | chr2 | 215392678 | ||||||
chr2:215392866
|
C | T | 1 | a0001c0042t0001g0148 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.4069+65G>A | FN1 | ENSG00000115414.21 | transcript | ENST00000354785.11 | protein_coding | 25/45 | chr2 | 215392866 | ||||||
chr2:215392896
|
T | C | 1 | a0001c0005t0001g0229 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.4069+35A>G | FN1 | ENSG00000115414.21 | transcript | ENST00000354785.11 | protein_coding | 25/45 | chr2 | 215392896 | ||||||
chr2:215392910
|
G | A | 7 | a0001c0002t0001g0113a0001c0009t0002g0167a0001c0044t0001g0065others(4): Show | 7 | HG02055.hp2 HG02258.hp2 HG02723.hp2 others(4): Show |
intron_variant | MODIFIER | c.4069+21C>T | FN1 | ENSG00000115414.21 | transcript | ENST00000354785.11 | protein_coding | 25/45 | chr2 | 215392910 | ||||||
chr2:215393226
|
GA | G | 32 | a0001c0001t0001g0177a0001c0002t0001g0113a0001c0005t0001g0214others(29): Show | 32 | HG00140.hp1 HG01099.hp1 HG01256.hp2 others(29): Show |
intron_variant | MODIFIER | c.3797-24delT | FN1 | ENSG00000115414.21 | transcript | ENST00000354785.11 | protein_coding | 24/45 | chr2 | 215393226 | ||||||
chr2:215393247
|
T | C | 3 | a0002c0008t0001g0027a0002c0022t0001g0014a0002c0022t0001g0015 | 3 | HG01261.hp2 HG01952.hp1 HG03669.hp2 |
intron_variant | MODIFIER | c.3797-44A>G | FN1 | ENSG00000115414.21 | transcript | ENST00000354785.11 | protein_coding | 24/45 | chr2 | 215393247 | ||||||
chr2:215393418
|
C | A | 1 | a0002c0003t0001g0037 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.3797-215G>T | FN1 | ENSG00000115414.21 | transcript | ENST00000354785.11 | protein_coding | 24/45 | chr2 | 215393418 | ||||||
chr2:215393427
|
A | AAT | 198 | a0001c0001t0001g0002a0001c0001t0001g0062a0001c0001t0001g0149others(195): Show | 200 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(197): Show |
intron_variant | MODIFIER | c.3797-226_3797-225d others(4): Show |
FN1 | ENSG00000115414.21 | transcript | ENST00000354785.11 | protein_coding | 24/45 | chr2 | 215393427 | ||||||
chr2:215393427
|
A | AATAT | 5 | a0001c0002t0001g0133a0001c0002t0001g0134a0001c0002t0001g0137others(2): Show | 5 | HG02145.hp1 HG02258.hp1 HG02451.hp2 others(2): Show |
intron_variant | MODIFIER | c.3797-228_3797-225d others(6): Show |
FN1 | ENSG00000115414.21 | transcript | ENST00000354785.11 | protein_coding | 24/45 | chr2 | 215393427 | ||||||
chr2:215393446
|
T | A | 75 | a0001c0001t0001g0002a0001c0001t0001g0062a0001c0001t0001g0149others(72): Show | 76 | HG00099.hp2 HG00280.hp2 HG00609.hp1 others(73): Show |
intron_variant | MODIFIER | c.3797-243A>T | FN1 | ENSG00000115414.21 | transcript | ENST00000354785.11 | protein_coding | 24/45 | chr2 | 215393446 | ||||||
chr2:215393485
|
A | C | 2 | a0001c0004t0001g0083a0001c0004t0001g0084 | 2 | HG01168.hp2 HG01169.hp1 |
intron_variant | MODIFIER | c.3797-282T>G | FN1 | ENSG00000115414.21 | transcript | ENST00000354785.11 | protein_coding | 24/45 | chr2 | 215393485 | ||||||
chr2:215393528
|
A | G | 198 | a0001c0001t0001g0002a0001c0001t0001g0062a0001c0001t0001g0149others(195): Show | 200 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(197): Show |
intron_variant | MODIFIER | c.3797-325T>C | FN1 | ENSG00000115414.21 | transcript | ENST00000354785.11 | protein_coding | 24/45 | chr2 | 215393528 | ||||||
chr2:215393579
|
C | A | 1 | a0001c0006t0003g0073 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.3797-376G>T | FN1 | ENSG00000115414.21 | transcript | ENST00000354785.11 | protein_coding | 24/45 | chr2 | 215393579 | ||||||
chr2:215393713
|
T | C | 2 | a0002c0003t0001g0026a0002c0003t0001g0030 | 2 | HG04115.hp2 HG04228.hp1 |
intron_variant | MODIFIER | c.3797-510A>G | FN1 | ENSG00000115414.21 | transcript | ENST00000354785.11 | protein_coding | 24/45 | chr2 | 215393713 | ||||||
chr2:215393858
|
G | A | 1 | a0001c0042t0001g0148 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.3797-655C>T | FN1 | ENSG00000115414.21 | transcript | ENST00000354785.11 | protein_coding | 24/45 | chr2 | 215393858 | ||||||
chr2:215393934
|
TAGAC | T | 9 | a0001c0006t0001g0069a0001c0006t0001g0072a0001c0006t0001g0075others(6): Show | 9 | HG00140.hp1 HG01099.hp1 HG01256.hp2 others(6): Show |
intron_variant | MODIFIER | c.3796+590_3796+593d others(6): Show |
FN1 | ENSG00000115414.21 | transcript | ENST00000354785.11 | protein_coding | 24/45 | chr2 | 215393934 | ||||||
chr2:215394756
|
G | A | 4 | a0002c0003t0001g0039a0002c0003t0001g0040a0002c0008t0001g0021others(1): Show | 4 | HG00741.hp2 HG01167.hp2 HG01175.hp2 others(1): Show |
intron_variant | MODIFIER | c.3605-37C>T | FN1 | ENSG00000115414.21 | transcript | ENST00000354785.11 | protein_coding | 23/45 | chr2 | 215394756 | ||||||
chr2:215394865
|
G | T | 6 | a0001c0009t0001g0155a0001c0009t0001g0157a0003c0007t0001g0160others(3): Show | 6 | HG02559.hp2 HG02630.hp1 HG02717.hp1 others(3): Show |
intron_variant | MODIFIER | c.3605-146C>A | FN1 | ENSG00000115414.21 | transcript | ENST00000354785.11 | protein_coding | 23/45 | chr2 | 215394865 | ||||||
chr2:215394911
|
A | T | 1 | a0001c0004t0001g0086 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.3605-192T>A | FN1 | ENSG00000115414.21 | transcript | ENST00000354785.11 | protein_coding | 23/45 | chr2 | 215394911 | ||||||
chr2:215394980
|
T | C | 3 | a0001c0002t0001g0140a0001c0002t0001g0144a0001c0060t0001g0132 | 3 | HG03453.hp2 HG03486.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.3605-261A>G | FN1 | ENSG00000115414.21 | transcript | ENST00000354785.11 | protein_coding | 23/45 | chr2 | 215394980 | ||||||
chr2:215395154
|
G | A | 13 | a0001c0002t0001g0133a0001c0002t0001g0134a0001c0002t0001g0135others(10): Show | 13 | HG01109.hp2 HG01884.hp1 HG02145.hp1 others(10): Show |
intron_variant | MODIFIER | c.3605-435C>T | FN1 | ENSG00000115414.21 | transcript | ENST00000354785.11 | protein_coding | 23/45 | chr2 | 215395154 | ||||||
chr2:215395155
|
C | T | 155 | a0001c0001t0001g0002a0001c0001t0001g0062a0001c0001t0001g0149others(152): Show | 156 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(153): Show |
intron_variant | MODIFIER | c.3605-436G>A | FN1 | ENSG00000115414.21 | transcript | ENST00000354785.11 | protein_coding | 23/45 | chr2 | 215395155 | ||||||
chr2:215395266
|
C | G | 152 | a0001c0001t0001g0002a0001c0001t0001g0062a0001c0001t0001g0149others(149): Show | 153 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(150): Show |
intron_variant | MODIFIER | c.3605-547G>C | FN1 | ENSG00000115414.21 | transcript | ENST00000354785.11 | protein_coding | 23/45 | chr2 | 215395266 | ||||||
chr2:215395272
|
C | T | 9 | a0001c0015t0001g0101a0001c0015t0001g0102a0001c0015t0001g0103others(6): Show | 9 | HG02055.hp1 HG02572.hp1 HG02622.hp2 others(6): Show |
intron_variant | MODIFIER | c.3605-553G>A | FN1 | ENSG00000115414.21 | transcript | ENST00000354785.11 | protein_coding | 23/45 | chr2 | 215395272 | ||||||
chr2:215395329
|
G | A | 1 | a0001c0006t0001g0110 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.3605-610C>T | FN1 | ENSG00000115414.21 | transcript | ENST00000354785.11 | protein_coding | 23/45 | chr2 | 215395329 | ||||||
chr2:215395457
|
T | C | 26 | a0001c0002t0001g0111a0001c0002t0001g0112a0001c0002t0001g0113others(23): Show | 26 | HG00140.hp2 HG00323.hp2 HG00642.hp2 others(23): Show |
intron_variant | MODIFIER | c.3605-738A>G | FN1 | ENSG00000115414.21 | transcript | ENST00000354785.11 | protein_coding | 23/45 | chr2 | 215395457 | ||||||
chr2:215395539
|
C | CA | 5 | a0002c0003t0001g0026a0002c0003t0001g0030a0002c0023t0001g0049others(2): Show | 5 | HG01891.hp2 HG02257.hp2 HG02559.hp1 others(2): Show |
intron_variant | MODIFIER | c.3605-821dupT | FN1 | ENSG00000115414.21 | transcript | ENST00000354785.11 | protein_coding | 23/45 | chr2 | 215395539 | ||||||
chr2:215395539
|
C | CAA | 13 | a0001c0002t0001g0133a0001c0002t0001g0134a0001c0002t0001g0135others(10): Show | 13 | HG01109.hp2 HG01884.hp1 HG02145.hp1 others(10): Show |
intron_variant | MODIFIER | c.3605-822_3605-821d others(4): Show |
FN1 | ENSG00000115414.21 | transcript | ENST00000354785.11 | protein_coding | 23/45 | chr2 | 215395539 | ||||||
chr2:215395539
|
CA | C | 139 | a0001c0001t0001g0002a0001c0001t0001g0062a0001c0001t0001g0149others(136): Show | 140 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(137): Show |
intron_variant | MODIFIER | c.3605-821delT | FN1 | ENSG00000115414.21 | transcript | ENST00000354785.11 | protein_coding | 23/45 | chr2 | 215395539 | ||||||
chr2:215395575
|
A | G | 47 | a0001c0002t0001g0111a0001c0002t0001g0112a0001c0002t0001g0113others(44): Show | 47 | HG00140.hp2 HG00323.hp2 HG00642.hp2 others(44): Show |
intron_variant | MODIFIER | c.3605-856T>C | FN1 | ENSG00000115414.21 | transcript | ENST00000354785.11 | protein_coding | 23/45 | chr2 | 215395575 | ||||||
chr2:215395834
|
G | A | 139 | a0001c0001t0001g0002a0001c0001t0001g0062a0001c0001t0001g0149others(136): Show | 140 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(137): Show |
intron_variant | MODIFIER | c.3605-1115C>T | FN1 | ENSG00000115414.21 | transcript | ENST00000354785.11 | protein_coding | 23/45 | chr2 | 215395834 | ||||||
chr2:215395899
|
G | T | 9 | a0001c0015t0001g0101a0001c0015t0001g0102a0001c0015t0001g0103others(6): Show | 9 | HG02055.hp1 HG02572.hp1 HG02622.hp2 others(6): Show |
intron_variant | MODIFIER | c.3605-1180C>A | FN1 | ENSG00000115414.21 | transcript | ENST00000354785.11 | protein_coding | 23/45 | chr2 | 215395899 | ||||||
chr2:215395908
|
CAACTT | C | 139 | a0001c0001t0001g0002a0001c0001t0001g0062a0001c0001t0001g0149others(136): Show | 140 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(137): Show |
intron_variant | MODIFIER | c.3605-1194_3605-119 others(9): Show |
FN1 | ENSG00000115414.21 | transcript | ENST00000354785.11 | protein_coding | 23/45 | chr2 | 215395908 | ||||||
chr2:215395996
|
C | A | 5 | a0001c0015t0001g0101a0001c0015t0001g0102a0001c0015t0001g0103others(2): Show | 5 | HG02055.hp1 HG02622.hp2 HG02896.hp2 others(2): Show |
intron_variant | MODIFIER | c.3604+1141G>T | FN1 | ENSG00000115414.21 | transcript | ENST00000354785.11 | protein_coding | 23/45 | chr2 | 215395996 | ||||||
chr2:215396364
|
G | A | 139 | a0001c0001t0001g0002a0001c0001t0001g0062a0001c0001t0001g0149others(136): Show | 140 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(137): Show |
intron_variant | MODIFIER | c.3604+773C>T | FN1 | ENSG00000115414.21 | transcript | ENST00000354785.11 | protein_coding | 23/45 | chr2 | 215396364 | ||||||
chr2:215397128
|
C | T | 1 | a0001c0025t0001g0163 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.3604+9G>A | FN1 | ENSG00000115414.21 | transcript | ENST00000354785.11 | protein_coding | 23/45 | chr2 | 215397128 | ||||||
chr2:215397401
|
TTC | T | 78 | a0001c0001t0001g0002a0001c0001t0001g0062a0001c0001t0001g0149others(75): Show | 79 | HG00099.hp2 HG00280.hp2 HG00609.hp1 others(76): Show |
intron_variant | MODIFIER | c.3518-180_3518-179d others(4): Show |
FN1 | ENSG00000115414.21 | transcript | ENST00000354785.11 | protein_coding | 22/45 | chr2 | 215397401 | ||||||
chr2:215397403
|
C | T | 63 | a0001c0002t0001g0111a0001c0002t0001g0112a0001c0002t0001g0113others(60): Show | 63 | HG00140.hp2 HG00323.hp2 HG00642.hp2 others(60): Show |
intron_variant | MODIFIER | c.3518-180G>A | FN1 | ENSG00000115414.21 | transcript | ENST00000354785.11 | protein_coding | 22/45 | chr2 | 215397403 | ||||||
chr2:215397579
|
CT | C | 7 | a0001c0011t0001g0106a0001c0011t0001g0107a0001c0011t0001g0108others(4): Show | 7 | HG01168.hp1 HG01243.hp2 HG01346.hp1 others(4): Show |
intron_variant | MODIFIER | c.3517+100delA | FN1 | ENSG00000115414.21 | transcript | ENST00000354785.11 | protein_coding | 22/45 | chr2 | 215397579 | ||||||
chr2:215397624
|
T | C | 9 | a0001c0015t0001g0101a0001c0015t0001g0102a0001c0015t0001g0103others(6): Show | 9 | HG02055.hp1 HG02572.hp1 HG02622.hp2 others(6): Show |
intron_variant | MODIFIER | c.3517+56A>G | FN1 | ENSG00000115414.21 | transcript | ENST00000354785.11 | protein_coding | 22/45 | chr2 | 215397624 | ||||||
chr2:215397677
|
T | C | 1 | a0006c0024t0001g0061 | 1 | HG02965.hp2 | splice_region_variant&intron_variant | LOW | c.3517+3A>G | FN1 | ENSG00000115414.21 | transcript | ENST00000354785.11 | protein_coding | 22/45 | chr2 | 215397677 | ||||||
chr2:215397868
|
G | C | 3 | a0001c0005t0001g0229a0011c0026t0001g0161a0011c0026t0001g0172 | 3 | HG02615.hp2 HG03209.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.3349-20C>G | FN1 | ENSG00000115414.21 | transcript | ENST00000354785.11 | protein_coding | 21/45 | chr2 | 215397868 | ||||||
chr2:215397898
|
A | C | 155 | a0001c0001t0001g0002a0001c0001t0001g0062a0001c0001t0001g0149others(152): Show | 156 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(153): Show |
intron_variant | MODIFIER | c.3349-50T>G | FN1 | ENSG00000115414.21 | transcript | ENST00000354785.11 | protein_coding | 21/45 | chr2 | 215397898 | ||||||
chr2:215398065
|
A | G | 142 | a0001c0001t0001g0002a0001c0001t0001g0062a0001c0001t0001g0149others(139): Show | 143 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(140): Show |
intron_variant | MODIFIER | c.3349-217T>C | FN1 | ENSG00000115414.21 | transcript | ENST00000354785.11 | protein_coding | 21/45 | chr2 | 215398065 | ||||||
chr2:215398533
|
A | G | 16 | a0001c0002t0001g0133a0001c0002t0001g0134a0001c0002t0001g0135others(13): Show | 16 | HG01109.hp2 HG01884.hp1 HG01891.hp2 others(13): Show |
intron_variant | MODIFIER | c.3349-685T>C | FN1 | ENSG00000115414.21 | transcript | ENST00000354785.11 | protein_coding | 21/45 | chr2 | 215398533 | ||||||
chr2:215398613
|
G | A | 141 | a0001c0001t0001g0002a0001c0001t0001g0062a0001c0001t0001g0149others(138): Show | 142 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(139): Show |
intron_variant | MODIFIER | c.3348+644C>T | FN1 | ENSG00000115414.21 | transcript | ENST00000354785.11 | protein_coding | 21/45 | chr2 | 215398613 | ||||||
chr2:215398643
|
G | A | 141 | a0001c0001t0001g0002a0001c0001t0001g0062a0001c0001t0001g0149others(138): Show | 142 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(139): Show |
intron_variant | MODIFIER | c.3348+614C>T | FN1 | ENSG00000115414.21 | transcript | ENST00000354785.11 | protein_coding | 21/45 | chr2 | 215398643 | ||||||
chr2:215398983
|
G | A | 141 | a0001c0001t0001g0002a0001c0001t0001g0062a0001c0001t0001g0149others(138): Show | 142 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(139): Show |
intron_variant | MODIFIER | c.3348+274C>T | FN1 | ENSG00000115414.21 | transcript | ENST00000354785.11 | protein_coding | 21/45 | chr2 | 215398983 | ||||||
chr2:215399203
|
C | A | 141 | a0001c0001t0001g0002a0001c0001t0001g0062a0001c0001t0001g0149others(138): Show | 142 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(139): Show |
intron_variant | MODIFIER | c.3348+54G>T | FN1 | ENSG00000115414.21 | transcript | ENST00000354785.11 | protein_coding | 21/45 | chr2 | 215399203 | ||||||
chr2:215399215
|
C | CT | 141 | a0001c0001t0001g0002a0001c0001t0001g0062a0001c0001t0001g0149others(138): Show | 142 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(139): Show |
intron_variant | MODIFIER | c.3348+41dupA | FN1 | ENSG00000115414.21 | transcript | ENST00000354785.11 | protein_coding | 21/45 | chr2 | 215399215 | ||||||
chr2:215399497
|
T | C | 1 | a0002c0022t0001g0015 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.3254-146A>G | FN1 | ENSG00000115414.21 | transcript | ENST00000354785.11 | protein_coding | 20/45 | chr2 | 215399497 | ||||||
chr2:215399547
|
G | C | 1 | a0001c0042t0001g0148 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.3254-196C>G | FN1 | ENSG00000115414.21 | transcript | ENST00000354785.11 | protein_coding | 20/45 | chr2 | 215399547 | ||||||
chr2:215399547
|
G | T | 57 | a0001c0004t0001g0001a0001c0004t0001g0068a0001c0004t0001g0070others(54): Show | 58 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(55): Show |
intron_variant | MODIFIER | c.3254-196C>A | FN1 | ENSG00000115414.21 | transcript | ENST00000354785.11 | protein_coding | 20/45 | chr2 | 215399547 | ||||||
chr2:215399715
|
T | A | 1 | a0001c0055t0001g0078 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.3254-364A>T | FN1 | ENSG00000115414.21 | transcript | ENST00000354785.11 | protein_coding | 20/45 | chr2 | 215399715 | ||||||
chr2:215399779
|
G | A | 1 | a0012c0047t0001g0186 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.3254-428C>T | FN1 | ENSG00000115414.21 | transcript | ENST00000354785.11 | protein_coding | 20/45 | chr2 | 215399779 | ||||||
chr2:215400023
|
A | C | 1 | a0003c0007t0002g0093 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.3254-672T>G | FN1 | ENSG00000115414.21 | transcript | ENST00000354785.11 | protein_coding | 20/45 | chr2 | 215400023 | ||||||
chr2:215400136
|
C | T | 132 | a0001c0001t0001g0002a0001c0001t0001g0062a0001c0001t0001g0149others(129): Show | 133 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(130): Show |
intron_variant | MODIFIER | c.3254-785G>A | FN1 | ENSG00000115414.21 | transcript | ENST00000354785.11 | protein_coding | 20/45 | chr2 | 215400136 | ||||||
chr2:215400182
|
C | T | 141 | a0001c0001t0001g0002a0001c0001t0001g0062a0001c0001t0001g0149others(138): Show | 142 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(139): Show |
intron_variant | MODIFIER | c.3254-831G>A | FN1 | ENSG00000115414.21 | transcript | ENST00000354785.11 | protein_coding | 20/45 | chr2 | 215400182 | ||||||
chr2:215400214
|
G | A | 2 | a0001c0002t0001g0124a0002c0033t0001g0018 | 2 | HG03704.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.3254-863C>T | FN1 | ENSG00000115414.21 | transcript | ENST00000354785.11 | protein_coding | 20/45 | chr2 | 215400214 | ||||||
chr2:215400379
|
T | C | 141 | a0001c0001t0001g0002a0001c0001t0001g0062a0001c0001t0001g0149others(138): Show | 142 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(139): Show |
intron_variant | MODIFIER | c.3254-1028A>G | FN1 | ENSG00000115414.21 | transcript | ENST00000354785.11 | protein_coding | 20/45 | chr2 | 215400379 | ||||||
chr2:215400478
|
G | A | 1 | a0001c0005t0001g0190 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.3254-1127C>T | FN1 | ENSG00000115414.21 | transcript | ENST00000354785.11 | protein_coding | 20/45 | chr2 | 215400478 | ||||||
chr2:215400523
|
A | G | 141 | a0001c0001t0001g0002a0001c0001t0001g0062a0001c0001t0001g0149others(138): Show | 142 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(139): Show |
intron_variant | MODIFIER | c.3254-1172T>C | FN1 | ENSG00000115414.21 | transcript | ENST00000354785.11 | protein_coding | 20/45 | chr2 | 215400523 | ||||||
chr2:215400579
|
T | C | 6 | a0001c0009t0001g0155a0001c0009t0001g0157a0003c0007t0001g0160others(3): Show | 6 | HG02559.hp2 HG02630.hp1 HG02717.hp1 others(3): Show |
intron_variant | MODIFIER | c.3254-1228A>G | FN1 | ENSG00000115414.21 | transcript | ENST00000354785.11 | protein_coding | 20/45 | chr2 | 215400579 | ||||||
chr2:215400735
|
G | A | 1 | a0001c0025t0001g0163 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.3254-1384C>T | FN1 | ENSG00000115414.21 | transcript | ENST00000354785.11 | protein_coding | 20/45 | chr2 | 215400735 | ||||||
chr2:215400751
|
C | CA | 117 | a0001c0001t0001g0002a0001c0001t0001g0062a0001c0001t0001g0149others(114): Show | 118 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(115): Show |
intron_variant | MODIFIER | c.3254-1401dupT | FN1 | ENSG00000115414.21 | transcript | ENST00000354785.11 | protein_coding | 20/45 | chr2 | 215400751 | ||||||
chr2:215400751
|
C | CAA | 32 | a0001c0001t0001g0171a0001c0001t0001g0173a0001c0001t0001g0183others(29): Show | 32 | HG00738.hp1 HG00738.hp2 HG01099.hp1 others(29): Show |
intron_variant | MODIFIER | c.3254-1402_3254-140 others(6): Show |
FN1 | ENSG00000115414.21 | transcript | ENST00000354785.11 | protein_coding | 20/45 | chr2 | 215400751 | ||||||
chr2:215400751
|
C | CAAA | 5 | a0001c0002t0001g0111a0001c0009t0001g0074a0001c0009t0002g0167others(2): Show | 5 | HG02055.hp1 HG02109.hp2 HG02280.hp1 others(2): Show |
intron_variant | MODIFIER | c.3254-1403_3254-140 others(7): Show |
FN1 | ENSG00000115414.21 | transcript | ENST00000354785.11 | protein_coding | 20/45 | chr2 | 215400751 | ||||||
chr2:215400751
|
CA | C | 46 | a0001c0004t0001g0001a0001c0004t0001g0068a0001c0004t0001g0070others(43): Show | 47 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(44): Show |
intron_variant | MODIFIER | c.3254-1401delT | FN1 | ENSG00000115414.21 | transcript | ENST00000354785.11 | protein_coding | 20/45 | chr2 | 215400751 | ||||||
chr2:215400873
|
G | A | 141 | a0001c0001t0001g0002a0001c0001t0001g0062a0001c0001t0001g0149others(138): Show | 142 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(139): Show |
intron_variant | MODIFIER | c.3254-1522C>T | FN1 | ENSG00000115414.21 | transcript | ENST00000354785.11 | protein_coding | 20/45 | chr2 | 215400873 | ||||||
chr2:215400877
|
C | T | 141 | a0001c0001t0001g0002a0001c0001t0001g0062a0001c0001t0001g0149others(138): Show | 142 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(139): Show |
intron_variant | MODIFIER | c.3254-1526G>A | FN1 | ENSG00000115414.21 | transcript | ENST00000354785.11 | protein_coding | 20/45 | chr2 | 215400877 | ||||||
chr2:215400916
|
C | T | 1 | a0002c0003t0001g0029 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.3254-1565G>A | FN1 | ENSG00000115414.21 | transcript | ENST00000354785.11 | protein_coding | 20/45 | chr2 | 215400916 | ||||||
chr2:215401061
|
G | A | 141 | a0001c0001t0001g0002a0001c0001t0001g0062a0001c0001t0001g0149others(138): Show | 142 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(139): Show |
intron_variant | MODIFIER | c.3254-1710C>T | FN1 | ENSG00000115414.21 | transcript | ENST00000354785.11 | protein_coding | 20/45 | chr2 | 215401061 | ||||||
chr2:215401071
|
C | CA | 5 | a0001c0001t0001g0175a0001c0001t0001g0217a0001c0005t0001g0176others(2): Show | 5 | HG00642.hp1 HG01928.hp2 HG01978.hp2 others(2): Show |
intron_variant | MODIFIER | c.3254-1721dupT | FN1 | ENSG00000115414.21 | transcript | ENST00000354785.11 | protein_coding | 20/45 | chr2 | 215401071 | ||||||
chr2:215401095
|
CAAA | C | 140 | a0001c0001t0001g0002a0001c0001t0001g0062a0001c0001t0001g0149others(137): Show | 141 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(138): Show |
intron_variant | MODIFIER | c.3254-1747_3254-174 others(7): Show |
FN1 | ENSG00000115414.21 | transcript | ENST00000354785.11 | protein_coding | 20/45 | chr2 | 215401095 | ||||||
chr2:215401125
|
A | G | 1 | a0001c0041t0001g0147 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.3254-1774T>C | FN1 | ENSG00000115414.21 | transcript | ENST00000354785.11 | protein_coding | 20/45 | chr2 | 215401125 | ||||||
chr2:215401156
|
TAAGA | T | 93 | a0001c0002t0001g0133a0001c0002t0001g0134a0001c0002t0001g0135others(90): Show | 94 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(91): Show |
intron_variant | MODIFIER | c.3254-1809_3254-180 others(8): Show |
FN1 | ENSG00000115414.21 | transcript | ENST00000354785.11 | protein_coding | 20/45 | chr2 | 215401156 | ||||||
chr2:215401169
|
A | G | 3 | a0001c0004t0001g0068a0001c0006t0001g0090a0001c0006t0001g0091 | 3 | HG00735.hp2 HG01256.hp2 HG01258.hp1 |
intron_variant | MODIFIER | c.3254-1818T>C | FN1 | ENSG00000115414.21 | transcript | ENST00000354785.11 | protein_coding | 20/45 | chr2 | 215401169 | ||||||
chr2:215401178
|
A | T | 3 | a0001c0004t0001g0068a0001c0006t0001g0090a0001c0006t0001g0091 | 3 | HG00735.hp2 HG01256.hp2 HG01258.hp1 |
intron_variant | MODIFIER | c.3254-1827T>A | FN1 | ENSG00000115414.21 | transcript | ENST00000354785.11 | protein_coding | 20/45 | chr2 | 215401178 | ||||||
chr2:215401182
|
T | A | 3 | a0001c0004t0001g0068a0001c0006t0001g0090a0001c0006t0001g0091 | 3 | HG00735.hp2 HG01256.hp2 HG01258.hp1 |
intron_variant | MODIFIER | c.3254-1831A>T | FN1 | ENSG00000115414.21 | transcript | ENST00000354785.11 | protein_coding | 20/45 | chr2 | 215401182 | ||||||
chr2:215401187
|
G | A | 3 | a0001c0004t0001g0068a0001c0006t0001g0090a0001c0006t0001g0091 | 3 | HG00735.hp2 HG01256.hp2 HG01258.hp1 |
intron_variant | MODIFIER | c.3254-1836C>T | FN1 | ENSG00000115414.21 | transcript | ENST00000354785.11 | protein_coding | 20/45 | chr2 | 215401187 | ||||||
chr2:215401197
|
G | A | 2 | a0001c0006t0001g0090a0001c0006t0001g0091 | 2 | HG01256.hp2 HG01258.hp1 |
intron_variant | MODIFIER | c.3254-1846C>T | FN1 | ENSG00000115414.21 | transcript | ENST00000354785.11 | protein_coding | 20/45 | chr2 | 215401197 | ||||||
chr2:215401198
|
A | G | 56 | a0001c0002t0001g0111a0001c0002t0001g0112a0001c0002t0001g0113others(53): Show | 56 | HG00140.hp2 HG00323.hp2 HG00642.hp2 others(53): Show |
intron_variant | MODIFIER | c.3254-1847T>C | FN1 | ENSG00000115414.21 | transcript | ENST00000354785.11 | protein_coding | 20/45 | chr2 | 215401198 | ||||||
chr2:215401205
|
A | AG | 7 | a0001c0011t0001g0106a0001c0011t0001g0107a0001c0011t0001g0108others(4): Show | 7 | HG01168.hp1 HG01243.hp2 HG01346.hp1 others(4): Show |
intron_variant | MODIFIER | c.3254-1855dupC | FN1 | ENSG00000115414.21 | transcript | ENST00000354785.11 | protein_coding | 20/45 | chr2 | 215401205 | ||||||
chr2:215401205
|
A | G | 1 | a0002c0003t0001g0044 | 1 | NA18943.hp2 | intron_variant | MODIFIER | c.3254-1854T>C | FN1 | ENSG00000115414.21 | transcript | ENST00000354785.11 | protein_coding | 20/45 | chr2 | 215401205 | ||||||
chr2:215401219
|
AAAGAAAG others(25): Show |
A | 1 | a0001c0062t0003g0136 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.3254-1900_3254-186 others(36): Show |
FN1 | ENSG00000115414.21 | transcript | ENST00000354785.11 | protein_coding | 20/45 | chr2 | 215401219 | ||||||
chr2:215401223
|
A | AAAGGAAG others(5): Show |
3 | a0002c0014t0001g0052a0002c0014t0001g0053a0002c0014t0001g0054 | 3 | HG01884.hp2 HG01975.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.3254-1873_3254-187 others(16): Show |
FN1 | ENSG00000115414.21 | transcript | ENST00000354785.11 | protein_coding | 20/45 | chr2 | 215401223 | ||||||
chr2:215401223
|
AAAGAAAG others(21): Show |
A | 1 | a0001c0001t0001g0169 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.3254-1900_3254-187 others(32): Show |
FN1 | ENSG00000115414.21 | transcript | ENST00000354785.11 | protein_coding | 20/45 | chr2 | 215401223 | ||||||
chr2:215401227
|
A | AAAGGAAG others(9): Show |
1 | a0001c0046t0001g0164 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.3254-1877_3254-187 others(20): Show |
FN1 | ENSG00000115414.21 | transcript | ENST00000354785.11 | protein_coding | 20/45 | chr2 | 215401227 | ||||||
chr2:215401227
|
A | G | 3 | a0002c0014t0001g0052a0002c0014t0001g0053a0002c0014t0001g0054 | 3 | HG01884.hp2 HG01975.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.3254-1876T>C | FN1 | ENSG00000115414.21 | transcript | ENST00000354785.11 | protein_coding | 20/45 | chr2 | 215401227 | ||||||
chr2:215401231
|
A | G | 4 | a0001c0046t0001g0164a0002c0014t0001g0052a0002c0014t0001g0053others(1): Show | 4 | HG01884.hp2 HG01975.hp1 HG02055.hp2 others(1): Show |
intron_variant | MODIFIER | c.3254-1880T>C | FN1 | ENSG00000115414.21 | transcript | ENST00000354785.11 | protein_coding | 20/45 | chr2 | 215401231 | ||||||
chr2:215401234
|
G | GAAAGAAA others(9): Show |
1 | a0002c0023t0001g0051 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.3254-1884_3254-188 others(20): Show |
FN1 | ENSG00000115414.21 | transcript | ENST00000354785.11 | protein_coding | 20/45 | chr2 | 215401234 | ||||||
chr2:215401234
|
G | GAAAGAAA others(13): Show |
5 | a0001c0044t0001g0065a0004c0019t0001g0004a0004c0019t0001g0007others(2): Show | 5 | HG02257.hp2 HG02258.hp2 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.3254-1884_3254-188 others(24): Show |
FN1 | ENSG00000115414.21 | transcript | ENST00000354785.11 | protein_coding | 20/45 | chr2 | 215401234 | ||||||
chr2:215401234
|
G | GAAAGAAA others(17): Show |
2 | a0001c0012t0001g0154a0001c0025t0001g0162 | 2 | HG02258.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.3254-1884_3254-188 others(28): Show |
FN1 | ENSG00000115414.21 | transcript | ENST00000354785.11 | protein_coding | 20/45 | chr2 | 215401234 | ||||||
chr2:215401235
|
A | AAAGGAAG others(21): Show |
1 | a0001c0025t0001g0163 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.3254-1885_3254-188 others(32): Show |
FN1 | ENSG00000115414.21 | transcript | ENST00000354785.11 | protein_coding | 20/45 | chr2 | 215401235 | ||||||
chr2:215401235
|
A | G | 7 | a0001c0002t0001g0123a0001c0027t0001g0063a0001c0045t0001g0165others(4): Show | 7 | HG00323.hp2 HG01884.hp2 HG01975.hp1 others(4): Show |
intron_variant | MODIFIER | c.3254-1884T>C | FN1 | ENSG00000115414.21 | transcript | ENST00000354785.11 | protein_coding | 20/45 | chr2 | 215401235 | ||||||
chr2:215401235
|
AAAGAAAG others(9): Show |
A | 1 | a0002c0037t0001g0058 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.3254-1900_3254-188 others(20): Show |
FN1 | ENSG00000115414.21 | transcript | ENST00000354785.11 | protein_coding | 20/45 | chr2 | 215401235 | ||||||
chr2:215401238
|
G | GAAAGAAA others(5): Show |
3 | a0001c0002t0001g0139a0001c0002t0001g0140a0001c0060t0001g0132 | 3 | HG03139.hp2 HG03453.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.3254-1888_3254-188 others(16): Show |
FN1 | ENSG00000115414.21 | transcript | ENST00000354785.11 | protein_coding | 20/45 | chr2 | 215401238 | ||||||
chr2:215401238
|
G | GAAAGAAA others(9): Show |
2 | a0001c0002t0001g0142a0001c0042t0001g0148 | 2 | HG02486.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.3254-1888_3254-188 others(20): Show |
FN1 | ENSG00000115414.21 | transcript | ENST00000354785.11 | protein_coding | 20/45 | chr2 | 215401238 | ||||||
chr2:215401238
|
G | GAAAGAAA others(13): Show |
3 | a0001c0002t0001g0133a0001c0002t0001g0137a0001c0002t0001g0138 | 3 | HG01884.hp1 HG02451.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.3254-1888_3254-188 others(24): Show |
FN1 | ENSG00000115414.21 | transcript | ENST00000354785.11 | protein_coding | 20/45 | chr2 | 215401238 | ||||||
chr2:215401238
|
G | GAAAGAAA others(15): Show |
1 | a0001c0002t0001g0144 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.3254-1888_3254-188 others(26): Show |
FN1 | ENSG00000115414.21 | transcript | ENST00000354785.11 | protein_coding | 20/45 | chr2 | 215401238 | ||||||
chr2:215401239
|
A | G | 21 | a0001c0002t0001g0112a0001c0002t0001g0123a0001c0002t0001g0127others(18): Show | 21 | HG00140.hp2 HG00323.hp2 HG01109.hp1 others(18): Show |
intron_variant | MODIFIER | c.3254-1888T>C | FN1 | ENSG00000115414.21 | transcript | ENST00000354785.11 | protein_coding | 20/45 | chr2 | 215401239 | ||||||
chr2:215401239
|
AAAGAAAG others(5): Show |
A | 17 | a0001c0001t0001g0002a0001c0001t0001g0149a0001c0001t0001g0151others(14): Show | 18 | HG00609.hp2 HG00642.hp1 HG00741.hp1 others(15): Show |
intron_variant | MODIFIER | c.3254-1900_3254-188 others(16): Show |
FN1 | ENSG00000115414.21 | transcript | ENST00000354785.11 | protein_coding | 20/45 | chr2 | 215401239 | ||||||
chr2:215401240
|
AAGAAAGA others(4): Show |
A | 1 | a0001c0006t0001g0069 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.3254-1900_3254-189 others(15): Show |
FN1 | ENSG00000115414.21 | transcript | ENST00000354785.11 | protein_coding | 20/45 | chr2 | 215401240 | ||||||
chr2:215401243
|
A | AAAGGAAG others(17): Show |
1 | a0003c0007t0001g0160 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.3254-1893_3254-189 others(28): Show |
FN1 | ENSG00000115414.21 | transcript | ENST00000354785.11 | protein_coding | 20/45 | chr2 | 215401243 | ||||||
chr2:215401243
|
A | G | 30 | a0001c0002t0001g0112a0001c0002t0001g0114a0001c0002t0001g0121others(27): Show | 30 | HG00140.hp2 HG00323.hp2 HG00642.hp2 others(27): Show |
intron_variant | MODIFIER | c.3254-1892T>C | FN1 | ENSG00000115414.21 | transcript | ENST00000354785.11 | protein_coding | 20/45 | chr2 | 215401243 | ||||||
chr2:215401244
|
AAGAAAGG | A | 5 | a0001c0006t0001g0072a0001c0006t0001g0075a0001c0006t0002g0077others(2): Show | 5 | HG00140.hp1 HG02818.hp2 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.3254-1900_3254-189 others(11): Show |
FN1 | ENSG00000115414.21 | transcript | ENST00000354785.11 | protein_coding | 20/45 | chr2 | 215401244 | ||||||
chr2:215401247
|
A | G | 52 | a0001c0001t0001g0173a0001c0001t0001g0210a0001c0001t0001g0211others(49): Show | 52 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(49): Show |
intron_variant | MODIFIER | c.3254-1896T>C | FN1 | ENSG00000115414.21 | transcript | ENST00000354785.11 | protein_coding | 20/45 | chr2 | 215401247 | ||||||
chr2:215401247
|
AAAGG | A | 31 | a0001c0001t0001g0174a0001c0001t0001g0181a0001c0001t0001g0185others(28): Show | 31 | HG01168.hp2 HG01169.hp1 HG01256.hp1 others(28): Show |
intron_variant | MODIFIER | c.3254-1900_3254-189 others(8): Show |
FN1 | ENSG00000115414.21 | transcript | ENST00000354785.11 | protein_coding | 20/45 | chr2 | 215401247 | ||||||
chr2:215401247
|
AAAGGAAG others(4): Show |
A | 1 | a0001c0001t0001g0150 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.3254-1907_3254-189 others(15): Show |
FN1 | ENSG00000115414.21 | transcript | ENST00000354785.11 | protein_coding | 20/45 | chr2 | 215401247 | ||||||
chr2:215401251
|
G | A | 92 | a0001c0001t0001g0062a0001c0001t0001g0171a0001c0001t0001g0175others(89): Show | 93 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(90): Show |
intron_variant | MODIFIER | c.3254-1900C>T | FN1 | ENSG00000115414.21 | transcript | ENST00000354785.11 | protein_coding | 20/45 | chr2 | 215401251 | ||||||
chr2:215401251
|
GAAGA | G | 5 | a0001c0001t0001g0209a0001c0005t0001g0179a0001c0005t0001g0218others(2): Show | 5 | HG00099.hp2 HG00639.hp2 HG02965.hp1 others(2): Show |
intron_variant | MODIFIER | c.3254-1904_3254-190 others(8): Show |
FN1 | ENSG00000115414.21 | transcript | ENST00000354785.11 | protein_coding | 20/45 | chr2 | 215401251 | ||||||
chr2:215401251
|
GAAGAAAG others(1): Show |
G | 26 | a0001c0001t0001g0173a0001c0001t0001g0192a0001c0001t0001g0193others(23): Show | 26 | HG00280.hp2 HG00735.hp1 HG01106.hp2 others(23): Show |
intron_variant | MODIFIER | c.3254-1908_3254-190 others(12): Show |
FN1 | ENSG00000115414.21 | transcript | ENST00000354785.11 | protein_coding | 20/45 | chr2 | 215401251 | ||||||
chr2:215401255
|
A | G | 68 | a0001c0001t0001g0062a0001c0001t0001g0177a0001c0001t0001g0208others(65): Show | 68 | HG00140.hp2 HG00323.hp2 HG00642.hp2 others(65): Show |
intron_variant | MODIFIER | c.3254-1904T>C | FN1 | ENSG00000115414.21 | transcript | ENST00000354785.11 | protein_coding | 20/45 | chr2 | 215401255 | ||||||
chr2:215401259
|
A | AAAAAAAG others(21): Show |
2 | a0002c0023t0001g0049a0004c0020t0002g0005 | 2 | HG02559.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.3254-1909_3254-190 others(32): Show |
FN1 | ENSG00000115414.21 | transcript | ENST00000354785.11 | protein_coding | 20/45 | chr2 | 215401259 | ||||||
chr2:215401259
|
A | AAAAAAAG others(17): Show |
4 | a0001c0002t0001g0134a0001c0002t0001g0135a0001c0002t0001g0141others(1): Show | 4 | HG01109.hp2 HG02145.hp1 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.3254-1909_3254-190 others(28): Show |
FN1 | ENSG00000115414.21 | transcript | ENST00000354785.11 | protein_coding | 20/45 | chr2 | 215401259 | ||||||
chr2:215401259
|
A | AAAGAAAG others(5): Show |
2 | a0002c0003t0001g0045a0002c0022t0001g0014 | 2 | HG01952.hp1 HG02083.hp2 |
intron_variant | MODIFIER | c.3254-1909_3254-190 others(16): Show |
FN1 | ENSG00000115414.21 | transcript | ENST00000354785.11 | protein_coding | 20/45 | chr2 | 215401259 | ||||||
chr2:215401259
|
A | AAAGAAAG others(1): Show |
4 | a0001c0012t0001g0079a0002c0008t0001g0021a0002c0031t0001g0048others(1): Show | 4 | HG00099.hp1 HG01175.hp2 HG01496.hp1 others(1): Show |
intron_variant | MODIFIER | c.3254-1909_3254-190 others(12): Show |
FN1 | ENSG00000115414.21 | transcript | ENST00000354785.11 | protein_coding | 20/45 | chr2 | 215401259 | ||||||
chr2:215401259
|
A | AAAGG | 19 | a0001c0001t0001g0183a0001c0001t0001g0187a0001c0004t0001g0001others(16): Show | 20 | HG00280.hp1 HG00323.hp1 HG00609.hp1 others(17): Show |
intron_variant | MODIFIER | c.3254-1912_3254-190 others(8): Show |
FN1 | ENSG00000115414.21 | transcript | ENST00000354785.11 | protein_coding | 20/45 | chr2 | 215401259 | ||||||
chr2:215401259
|
A | G | 147 | a0001c0001t0001g0002a0001c0001t0001g0062a0001c0001t0001g0149others(144): Show | 148 | HG00099.hp2 HG00140.hp2 HG00323.hp2 others(145): Show |
intron_variant | MODIFIER | c.3254-1908T>C | FN1 | ENSG00000115414.21 | transcript | ENST00000354785.11 | protein_coding | 20/45 | chr2 | 215401259 | ||||||
chr2:215401261
|
A | G | 1 | a0003c0048t0002g0100 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.3254-1910T>C | FN1 | ENSG00000115414.21 | transcript | ENST00000354785.11 | protein_coding | 20/45 | chr2 | 215401261 | ||||||
chr2:215401263
|
G | A | 2 | a0001c0015t0001g0102a0003c0048t0002g0100 | 2 | HG02572.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.3254-1912C>T | FN1 | ENSG00000115414.21 | transcript | ENST00000354785.11 | protein_coding | 20/45 | chr2 | 215401263 | ||||||
chr2:215401263
|
G | GAAGGA | 6 | a0001c0015t0001g0101a0001c0015t0001g0103a0001c0015t0001g0104others(3): Show | 6 | HG02055.hp1 HG02622.hp2 HG02896.hp2 others(3): Show |
intron_variant | MODIFIER | c.3254-1917_3254-191 others(9): Show |
FN1 | ENSG00000115414.21 | transcript | ENST00000354785.11 | protein_coding | 20/45 | chr2 | 215401263 | ||||||
chr2:215401263
|
G | GAAGGAAG others(6): Show |
1 | a0001c0002t0001g0127 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.3254-1913_3254-191 others(17): Show |
FN1 | ENSG00000115414.21 | transcript | ENST00000354785.11 | protein_coding | 20/45 | chr2 | 215401263 | ||||||
chr2:215401263
|
G | GAAGGAAG others(10): Show |
4 | a0001c0002t0001g0123a0001c0002t0001g0128a0001c0002t0001g0129others(1): Show | 4 | HG00140.hp2 HG00323.hp2 HG01109.hp1 others(1): Show |
intron_variant | MODIFIER | c.3254-1913_3254-191 others(21): Show |
FN1 | ENSG00000115414.21 | transcript | ENST00000354785.11 | protein_coding | 20/45 | chr2 | 215401263 | ||||||
chr2:215401263
|
G | GAAGGAAG others(14): Show |
2 | a0001c0002t0001g0114a0001c0027t0001g0063 | 2 | HG00642.hp2 NA20805.hp2 |
intron_variant | MODIFIER | c.3254-1913_3254-191 others(25): Show |
FN1 | ENSG00000115414.21 | transcript | ENST00000354785.11 | protein_coding | 20/45 | chr2 | 215401263 | ||||||
chr2:215401263
|
G | GAAGGAAG others(19): Show |
2 | a0001c0009t0002g0167a0003c0007t0002g0066 | 2 | HG03471.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.3254-1913_3254-191 others(30): Show |
FN1 | ENSG00000115414.21 | transcript | ENST00000354785.11 | protein_coding | 20/45 | chr2 | 215401263 | ||||||
chr2:215401263
|
G | GAAGGAAG others(18): Show |
11 | a0001c0002t0001g0124a0001c0002t0001g0126a0001c0002t0001g0130others(8): Show | 11 | HG00738.hp1 HG00738.hp2 HG01243.hp2 others(8): Show |
intron_variant | MODIFIER | c.3254-1913_3254-191 others(29): Show |
FN1 | ENSG00000115414.21 | transcript | ENST00000354785.11 | protein_coding | 20/45 | chr2 | 215401263 | ||||||
chr2:215401263
|
G | GAAGGAAG others(23): Show |
1 | a0001c0045t0001g0165 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.3254-1913_3254-191 others(34): Show |
FN1 | ENSG00000115414.21 | transcript | ENST00000354785.11 | protein_coding | 20/45 | chr2 | 215401263 | ||||||
chr2:215401263
|
G | GAAGGAAG others(28): Show |
1 | a0001c0058t0002g0153 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.3254-1913_3254-191 others(39): Show |
FN1 | ENSG00000115414.21 | transcript | ENST00000354785.11 | protein_coding | 20/45 | chr2 | 215401263 | ||||||
chr2:215401263
|
G | GAAGGAAG others(22): Show |
5 | a0001c0002t0001g0112a0001c0002t0001g0121a0002c0014t0001g0056others(2): Show | 5 | HG01175.hp1 HG01243.hp1 HG01361.hp2 others(2): Show |
intron_variant | MODIFIER | c.3254-1913_3254-191 others(33): Show |
FN1 | ENSG00000115414.21 | transcript | ENST00000354785.11 | protein_coding | 20/45 | chr2 | 215401263 | ||||||
chr2:215401263
|
G | GAAGGAAG others(27): Show |
2 | a0005c0029t0003g0235a0005c0065t0001g0236 | 2 | HG03225.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.3254-1913_3254-191 others(38): Show |
FN1 | ENSG00000115414.21 | transcript | ENST00000354785.11 | protein_coding | 20/45 | chr2 | 215401263 | ||||||
chr2:215401263
|
G | GAAGGAAG others(37): Show |
1 | a0001c0006t0001g0110 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.3254-1913_3254-191 others(48): Show |
FN1 | ENSG00000115414.21 | transcript | ENST00000354785.11 | protein_coding | 20/45 | chr2 | 215401263 | ||||||
chr2:215401263
|
G | GAAGGAAG others(26): Show |
3 | a0001c0009t0001g0166a0003c0007t0002g0156a0006c0040t0001g0060 | 3 | HG02647.hp2 HG03453.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.3254-1913_3254-191 others(37): Show |
FN1 | ENSG00000115414.21 | transcript | ENST00000354785.11 | protein_coding | 20/45 | chr2 | 215401263 | ||||||
chr2:215401263
|
G | GAAGGAAG others(31): Show |
1 | a0005c0029t0003g0234 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.3254-1913_3254-191 others(42): Show |
FN1 | ENSG00000115414.21 | transcript | ENST00000354785.11 | protein_coding | 20/45 | chr2 | 215401263 | ||||||
chr2:215401263
|
G | GAAGGAAG others(30): Show |
6 | a0001c0002t0001g0111a0001c0002t0001g0122a0001c0002t0001g0232others(3): Show | 6 | HG01168.hp1 HG02280.hp1 HG02965.hp2 others(3): Show |
intron_variant | MODIFIER | c.3254-1913_3254-191 others(41): Show |
FN1 | ENSG00000115414.21 | transcript | ENST00000354785.11 | protein_coding | 20/45 | chr2 | 215401263 | ||||||
chr2:215401263
|
G | GAAGGAAG others(34): Show |
4 | a0001c0002t0001g0233a0001c0009t0001g0155a0001c0009t0001g0157others(1): Show | 4 | HG02630.hp1 HG02717.hp1 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.3254-1913_3254-191 others(45): Show |
FN1 | ENSG00000115414.21 | transcript | ENST00000354785.11 | protein_coding | 20/45 | chr2 | 215401263 | ||||||
chr2:215401263
|
G | GAAGGAAG others(38): Show |
3 | a0001c0002t0001g0113a0001c0002t0001g0119a0001c0027t0001g0120 | 3 | HG01099.hp2 HG01257.hp1 HG02895.hp1 |
intron_variant | MODIFIER | c.3254-1913_3254-191 others(49): Show |
FN1 | ENSG00000115414.21 | transcript | ENST00000354785.11 | protein_coding | 20/45 | chr2 | 215401263 | ||||||
chr2:215401263
|
G | GAAGGAAG others(42): Show |
1 | a0003c0007t0002g0159 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.3254-1913_3254-191 others(53): Show |
FN1 | ENSG00000115414.21 | transcript | ENST00000354785.11 | protein_coding | 20/45 | chr2 | 215401263 | ||||||
chr2:215401288
|
AAG | A | 78 | a0001c0004t0001g0001a0001c0004t0001g0068a0001c0004t0001g0070others(75): Show | 79 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(76): Show |
intron_variant | MODIFIER | c.3254-1939_3254-193 others(6): Show |
FN1 | ENSG00000115414.21 | transcript | ENST00000354785.11 | protein_coding | 20/45 | chr2 | 215401288 | ||||||
chr2:215401288
|
AAGAGAG | A | 19 | a0001c0002t0001g0133a0001c0002t0001g0134a0001c0002t0001g0135others(16): Show | 19 | HG01109.hp2 HG01261.hp2 HG01884.hp1 others(16): Show |
intron_variant | MODIFIER | c.3254-1943_3254-193 others(10): Show |
FN1 | ENSG00000115414.21 | transcript | ENST00000354785.11 | protein_coding | 20/45 | chr2 | 215401288 | ||||||
chr2:215401502
|
C | A | 58 | a0001c0004t0001g0001a0001c0004t0001g0068a0001c0004t0001g0070others(55): Show | 59 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(56): Show |
intron_variant | MODIFIER | c.3254-2151G>T | FN1 | ENSG00000115414.21 | transcript | ENST00000354785.11 | protein_coding | 20/45 | chr2 | 215401502 | ||||||
chr2:215401685
|
TCTCAA | T | 3 | a0002c0014t0001g0052a0002c0014t0001g0053a0002c0014t0001g0054 | 3 | HG01884.hp2 HG01975.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.3254-2339_3254-233 others(9): Show |
FN1 | ENSG00000115414.21 | transcript | ENST00000354785.11 | protein_coding | 20/45 | chr2 | 215401685 | ||||||
chr2:215401754
|
C | T | 1 | a0002c0031t0001g0048 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.3254-2403G>A | FN1 | ENSG00000115414.21 | transcript | ENST00000354785.11 | protein_coding | 20/45 | chr2 | 215401754 | ||||||
chr2:215401813
|
T | C | 78 | a0001c0001t0001g0002a0001c0001t0001g0062a0001c0001t0001g0149others(75): Show | 79 | HG00099.hp2 HG00280.hp2 HG00609.hp1 others(76): Show |
intron_variant | MODIFIER | c.3254-2462A>G | FN1 | ENSG00000115414.21 | transcript | ENST00000354785.11 | protein_coding | 20/45 | chr2 | 215401813 | ||||||
chr2:215402013
|
A | G | 74 | a0001c0002t0001g0133a0001c0002t0001g0134a0001c0002t0001g0135others(71): Show | 75 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(72): Show |
intron_variant | MODIFIER | c.3253+2376T>C | FN1 | ENSG00000115414.21 | transcript | ENST00000354785.11 | protein_coding | 20/45 | chr2 | 215402013 | ||||||
chr2:215402172
|
T | A | 1 | a0001c0005t0001g0178 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.3253+2217A>T | FN1 | ENSG00000115414.21 | transcript | ENST00000354785.11 | protein_coding | 20/45 | chr2 | 215402172 | ||||||
chr2:215402173
|
T | A | 1 | a0001c0005t0001g0178 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.3253+2216A>T | FN1 | ENSG00000115414.21 | transcript | ENST00000354785.11 | protein_coding | 20/45 | chr2 | 215402173 | ||||||
chr2:215402558
|
A | C | 9 | a0001c0015t0001g0101a0001c0015t0001g0102a0001c0015t0001g0103others(6): Show | 9 | HG02055.hp1 HG02572.hp1 HG02622.hp2 others(6): Show |
intron_variant | MODIFIER | c.3253+1831T>G | FN1 | ENSG00000115414.21 | transcript | ENST00000354785.11 | protein_coding | 20/45 | chr2 | 215402558 | ||||||
chr2:215402955
|
A | G | 2 | a0004c0019t0001g0004a0004c0019t0001g0007 | 2 | HG02647.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.3253+1434T>C | FN1 | ENSG00000115414.21 | transcript | ENST00000354785.11 | protein_coding | 20/45 | chr2 | 215402955 | ||||||
chr2:215403234
|
C | T | 1 | a0003c0007t0002g0066 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.3253+1155G>A | FN1 | ENSG00000115414.21 | transcript | ENST00000354785.11 | protein_coding | 20/45 | chr2 | 215403234 | ||||||
chr2:215403415
|
C | T | 1 | a0001c0010t0001g0230 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.3253+974G>A | FN1 | ENSG00000115414.21 | transcript | ENST00000354785.11 | protein_coding | 20/45 | chr2 | 215403415 | ||||||
chr2:215403470
|
T | C | 3 | a0002c0008t0001g0027a0002c0022t0001g0014a0002c0022t0001g0015 | 3 | HG01261.hp2 HG01952.hp1 HG03669.hp2 |
intron_variant | MODIFIER | c.3253+919A>G | FN1 | ENSG00000115414.21 | transcript | ENST00000354785.11 | protein_coding | 20/45 | chr2 | 215403470 | ||||||
chr2:215403632
|
G | A | 61 | a0001c0004t0001g0001a0001c0004t0001g0068a0001c0004t0001g0070others(58): Show | 62 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(59): Show |
intron_variant | MODIFIER | c.3253+757C>T | FN1 | ENSG00000115414.21 | transcript | ENST00000354785.11 | protein_coding | 20/45 | chr2 | 215403632 | ||||||
chr2:215403714
|
T | A | 3 | a0002c0023t0001g0049a0002c0023t0001g0051a0018c0038t0002g0050 | 3 | HG01891.hp2 HG02257.hp2 HG02559.hp1 |
intron_variant | MODIFIER | c.3253+675A>T | FN1 | ENSG00000115414.21 | transcript | ENST00000354785.11 | protein_coding | 20/45 | chr2 | 215403714 | ||||||
chr2:215403721
|
G | A | 78 | a0001c0001t0001g0002a0001c0001t0001g0062a0001c0001t0001g0149others(75): Show | 79 | HG00099.hp2 HG00280.hp2 HG00609.hp1 others(76): Show |
intron_variant | MODIFIER | c.3253+668C>T | FN1 | ENSG00000115414.21 | transcript | ENST00000354785.11 | protein_coding | 20/45 | chr2 | 215403721 | ||||||
chr2:215403852
|
T | C | 10 | a0001c0011t0001g0106a0001c0011t0001g0107a0001c0011t0001g0108others(7): Show | 10 | HG01168.hp1 HG01243.hp2 HG01255.hp2 others(7): Show |
intron_variant | MODIFIER | c.3253+537A>G | FN1 | ENSG00000115414.21 | transcript | ENST00000354785.11 | protein_coding | 20/45 | chr2 | 215403852 | ||||||
chr2:215403984
|
G | A | 1 | a0001c0025t0001g0163 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.3253+405C>T | FN1 | ENSG00000115414.21 | transcript | ENST00000354785.11 | protein_coding | 20/45 | chr2 | 215403984 | ||||||
chr2:215404079
|
G | A | 1 | a0001c0001t0001g0151 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.3253+310C>T | FN1 | ENSG00000115414.21 | transcript | ENST00000354785.11 | protein_coding | 20/45 | chr2 | 215404079 | ||||||
chr2:215404179
|
C | T | 78 | a0001c0001t0001g0002a0001c0001t0001g0062a0001c0001t0001g0149others(75): Show | 79 | HG00099.hp2 HG00280.hp2 HG00609.hp1 others(76): Show |
intron_variant | MODIFIER | c.3253+210G>A | FN1 | ENSG00000115414.21 | transcript | ENST00000354785.11 | protein_coding | 20/45 | chr2 | 215404179 | ||||||
chr2:215404230
|
G | A | 3 | a0002c0014t0001g0052a0002c0014t0001g0053a0002c0014t0001g0054 | 3 | HG01884.hp2 HG01975.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.3253+159C>T | FN1 | ENSG00000115414.21 | transcript | ENST00000354785.11 | protein_coding | 20/45 | chr2 | 215404230 | ||||||
chr2:215404256
|
A | G | 1 | a0001c0042t0001g0148 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.3253+133T>C | FN1 | ENSG00000115414.21 | transcript | ENST00000354785.11 | protein_coding | 20/45 | chr2 | 215404256 | ||||||
chr2:215404299
|
G | T | 1 | a0001c0004t0001g0071 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.3253+90C>A | FN1 | ENSG00000115414.21 | transcript | ENST00000354785.11 | protein_coding | 20/45 | chr2 | 215404299 | ||||||
chr2:215404307
|
T | G | 1 | a0016c0043t0001g0168 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.3253+82A>C | FN1 | ENSG00000115414.21 | transcript | ENST00000354785.11 | protein_coding | 20/45 | chr2 | 215404307 | ||||||
chr2:215404307
|
T | TTTTTG | 7 | a0001c0004t0001g0071a0001c0042t0001g0148a0002c0003t0001g0042others(4): Show | 7 | HG01070.hp2 HG01891.hp2 HG02257.hp2 others(4): Show |
intron_variant | MODIFIER | c.3253+81_3253+82ins others(5): Show |
FN1 | ENSG00000115414.21 | transcript | ENST00000354785.11 | protein_coding | 20/45 | chr2 | 215404307 | ||||||
chr2:215404307
|
T | TTTTTTG | 51 | a0001c0004t0001g0001a0001c0004t0001g0068a0001c0004t0001g0070others(48): Show | 52 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(49): Show |
intron_variant | MODIFIER | c.3253+81_3253+82ins others(6): Show |
FN1 | ENSG00000115414.21 | transcript | ENST00000354785.11 | protein_coding | 20/45 | chr2 | 215404307 | ||||||
chr2:215404308
|
G | T | 83 | a0001c0001t0001g0002a0001c0001t0001g0062a0001c0001t0001g0149others(80): Show | 84 | HG00099.hp2 HG00280.hp2 HG00609.hp1 others(81): Show |
intron_variant | MODIFIER | c.3253+81C>A | FN1 | ENSG00000115414.21 | transcript | ENST00000354785.11 | protein_coding | 20/45 | chr2 | 215404308 | ||||||
chr2:215404310
|
T | G | 77 | a0001c0001t0001g0002a0001c0001t0001g0062a0001c0001t0001g0149others(74): Show | 78 | HG00099.hp2 HG00280.hp2 HG00609.hp1 others(75): Show |
intron_variant | MODIFIER | c.3253+79A>C | FN1 | ENSG00000115414.21 | transcript | ENST00000354785.11 | protein_coding | 20/45 | chr2 | 215404310 | ||||||
chr2:215404323
|
G | T | 61 | a0001c0004t0001g0001a0001c0004t0001g0068a0001c0004t0001g0070others(58): Show | 62 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(59): Show |
intron_variant | MODIFIER | c.3253+66C>A | FN1 | ENSG00000115414.21 | transcript | ENST00000354785.11 | protein_coding | 20/45 | chr2 | 215404323 | ||||||
chr2:215404372
|
C | T | 61 | a0001c0004t0001g0001a0001c0004t0001g0068a0001c0004t0001g0070others(58): Show | 62 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(59): Show |
intron_variant | MODIFIER | c.3253+17G>A | FN1 | ENSG00000115414.21 | transcript | ENST00000354785.11 | protein_coding | 20/45 | chr2 | 215404372 | ||||||
chr2:215404889
|
G | A | 1 | a0001c0042t0001g0148 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.2987-234C>T | FN1 | ENSG00000115414.21 | transcript | ENST00000354785.11 | protein_coding | 19/45 | chr2 | 215404889 | ||||||
chr2:215404916
|
C | T | 6 | a0001c0015t0001g0101a0001c0015t0001g0102a0001c0015t0001g0103others(3): Show | 6 | HG02055.hp1 HG02622.hp2 HG02896.hp2 others(3): Show |
intron_variant | MODIFIER | c.2987-261G>A | FN1 | ENSG00000115414.21 | transcript | ENST00000354785.11 | protein_coding | 19/45 | chr2 | 215404916 | ||||||
chr2:215404917
|
G | A | 60 | a0001c0004t0001g0001a0001c0004t0001g0068a0001c0004t0001g0070others(57): Show | 61 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(58): Show |
intron_variant | MODIFIER | c.2987-262C>T | FN1 | ENSG00000115414.21 | transcript | ENST00000354785.11 | protein_coding | 19/45 | chr2 | 215404917 | ||||||
chr2:215405051
|
G | A | 13 | a0001c0002t0001g0133a0001c0002t0001g0134a0001c0002t0001g0135others(10): Show | 13 | HG01109.hp2 HG01884.hp1 HG02145.hp1 others(10): Show |
intron_variant | MODIFIER | c.2987-396C>T | FN1 | ENSG00000115414.21 | transcript | ENST00000354785.11 | protein_coding | 19/45 | chr2 | 215405051 | ||||||
chr2:215405186
|
G | C | 3 | a0002c0023t0001g0049a0002c0023t0001g0051a0018c0038t0002g0050 | 3 | HG01891.hp2 HG02257.hp2 HG02559.hp1 |
intron_variant | MODIFIER | c.2987-531C>G | FN1 | ENSG00000115414.21 | transcript | ENST00000354785.11 | protein_coding | 19/45 | chr2 | 215405186 | ||||||
chr2:215405423
|
T | A | 7 | a0001c0011t0001g0106a0001c0011t0001g0107a0001c0011t0001g0108others(4): Show | 7 | HG01168.hp1 HG01243.hp2 HG01346.hp1 others(4): Show |
intron_variant | MODIFIER | c.2987-768A>T | FN1 | ENSG00000115414.21 | transcript | ENST00000354785.11 | protein_coding | 19/45 | chr2 | 215405423 | ||||||
chr2:215405729
|
C | T | 4 | a0001c0041t0001g0147a0003c0048t0002g0100a0010c0028t0002g0237others(1): Show | 4 | HG02572.hp1 HG02886.hp1 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.2986+509G>A | FN1 | ENSG00000115414.21 | transcript | ENST00000354785.11 | protein_coding | 19/45 | chr2 | 215405729 | ||||||
chr2:215405781
|
C | T | 2 | a0001c0006t0001g0090a0001c0006t0001g0091 | 2 | HG01256.hp2 HG01258.hp1 |
intron_variant | MODIFIER | c.2986+457G>A | FN1 | ENSG00000115414.21 | transcript | ENST00000354785.11 | protein_coding | 19/45 | chr2 | 215405781 | ||||||
chr2:215406708
|
T | C | 1 | a0001c0010t0001g0230 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.2714-198A>G | FN1 | ENSG00000115414.21 | transcript | ENST00000354785.11 | protein_coding | 18/45 | chr2 | 215406708 | ||||||
chr2:215406787
|
A | T | 73 | a0001c0002t0001g0133a0001c0002t0001g0134a0001c0002t0001g0135others(70): Show | 74 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(71): Show |
intron_variant | MODIFIER | c.2714-277T>A | FN1 | ENSG00000115414.21 | transcript | ENST00000354785.11 | protein_coding | 18/45 | chr2 | 215406787 | ||||||
chr2:215406921
|
C | T | 57 | a0001c0004t0001g0001a0001c0004t0001g0068a0001c0004t0001g0070others(54): Show | 58 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(55): Show |
intron_variant | MODIFIER | c.2713+206G>A | FN1 | ENSG00000115414.21 | transcript | ENST00000354785.11 | protein_coding | 18/45 | chr2 | 215406921 | ||||||
chr2:215406952
|
C | G | 11 | a0001c0011t0001g0106a0001c0011t0001g0107a0001c0011t0001g0108others(8): Show | 11 | HG01168.hp1 HG01243.hp2 HG01255.hp2 others(8): Show |
intron_variant | MODIFIER | c.2713+175G>C | FN1 | ENSG00000115414.21 | transcript | ENST00000354785.11 | protein_coding | 18/45 | chr2 | 215406952 | ||||||
chr2:215407012
|
A | G | 1 | a0002c0032t0001g0012 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.2713+115T>C | FN1 | ENSG00000115414.21 | transcript | ENST00000354785.11 | protein_coding | 18/45 | chr2 | 215407012 | ||||||
chr2:215407040
|
A | T | 73 | a0001c0002t0001g0133a0001c0002t0001g0134a0001c0002t0001g0135others(70): Show | 74 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(71): Show |
intron_variant | MODIFIER | c.2713+87T>A | FN1 | ENSG00000115414.21 | transcript | ENST00000354785.11 | protein_coding | 18/45 | chr2 | 215407040 | ||||||
chr2:215407089
|
A | T | 57 | a0001c0004t0001g0001a0001c0004t0001g0068a0001c0004t0001g0070others(54): Show | 58 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(55): Show |
intron_variant | MODIFIER | c.2713+38T>A | FN1 | ENSG00000115414.21 | transcript | ENST00000354785.11 | protein_coding | 18/45 | chr2 | 215407089 | ||||||
chr2:215407743
|
C | G | 1 | a0001c0015t0001g0102 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.2518+365G>C | FN1 | ENSG00000115414.21 | transcript | ENST00000354785.11 | protein_coding | 17/45 | chr2 | 215407743 | ||||||
chr2:215407791
|
G | A | 27 | a0001c0002t0001g0111a0001c0002t0001g0112a0001c0002t0001g0113others(24): Show | 27 | HG00140.hp2 HG00323.hp2 HG00642.hp2 others(24): Show |
intron_variant | MODIFIER | c.2518+317C>T | FN1 | ENSG00000115414.21 | transcript | ENST00000354785.11 | protein_coding | 17/45 | chr2 | 215407791 | ||||||
chr2:215407946
|
CA | C | 88 | a0001c0001t0001g0002a0001c0001t0001g0062a0001c0001t0001g0149others(85): Show | 90 | HG00099.hp2 HG00280.hp2 HG00609.hp1 others(87): Show |
intron_variant | MODIFIER | c.2518+161delT | FN1 | ENSG00000115414.21 | transcript | ENST00000354785.11 | protein_coding | 17/45 | chr2 | 215407946 | ||||||
chr2:215407947
|
A | C | 52 | a0001c0002t0001g0134a0001c0002t0001g0141a0001c0002t0001g0142others(49): Show | 52 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(49): Show |
intron_variant | MODIFIER | c.2518+161T>G | FN1 | ENSG00000115414.21 | transcript | ENST00000354785.11 | protein_coding | 17/45 | chr2 | 215407947 | ||||||
chr2:215407947
|
A | G | 1 | a0001c0004t0001g0085 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.2518+161T>C | FN1 | ENSG00000115414.21 | transcript | ENST00000354785.11 | protein_coding | 17/45 | chr2 | 215407947 | ||||||
chr2:215407947
|
AC | A | 56 | a0001c0002t0001g0111a0001c0002t0001g0112a0001c0002t0001g0113others(53): Show | 56 | HG00140.hp2 HG00323.hp2 HG00642.hp2 others(53): Show |
intron_variant | MODIFIER | c.2518+160delG | FN1 | ENSG00000115414.21 | transcript | ENST00000354785.11 | protein_coding | 17/45 | chr2 | 215407947 | ||||||
chr2:215407953
|
G | C | 12 | a0001c0002t0001g0133a0001c0002t0001g0134a0001c0002t0001g0135others(9): Show | 12 | HG01109.hp2 HG01884.hp1 HG02145.hp1 others(9): Show |
intron_variant | MODIFIER | c.2518+155C>G | FN1 | ENSG00000115414.21 | transcript | ENST00000354785.11 | protein_coding | 17/45 | chr2 | 215407953 | ||||||
chr2:215407954
|
CCA | C | 127 | a0001c0002t0001g0111a0001c0002t0001g0112a0001c0002t0001g0113others(124): Show | 128 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(125): Show |
intron_variant | MODIFIER | c.2518+152_2518+153d others(4): Show |
FN1 | ENSG00000115414.21 | transcript | ENST00000354785.11 | protein_coding | 17/45 | chr2 | 215407954 | ||||||
chr2:215407954
|
CCACA | C | 89 | a0001c0001t0001g0002a0001c0001t0001g0062a0001c0001t0001g0149others(86): Show | 90 | HG00099.hp2 HG00280.hp2 HG00609.hp1 others(87): Show |
intron_variant | MODIFIER | c.2518+150_2518+153d others(6): Show |
FN1 | ENSG00000115414.21 | transcript | ENST00000354785.11 | protein_coding | 17/45 | chr2 | 215407954 | ||||||
chr2:215407954
|
CCACACA | C | 6 | a0001c0011t0001g0106a0001c0011t0001g0107a0001c0011t0001g0108others(3): Show | 6 | HG01168.hp1 HG01243.hp2 HG01346.hp1 others(3): Show |
intron_variant | MODIFIER | c.2518+148_2518+153d others(8): Show |
FN1 | ENSG00000115414.21 | transcript | ENST00000354785.11 | protein_coding | 17/45 | chr2 | 215407954 | ||||||
chr2:215407955
|
C | G | 12 | a0001c0002t0001g0133a0001c0002t0001g0134a0001c0002t0001g0135others(9): Show | 12 | HG01109.hp2 HG01884.hp1 HG02145.hp1 others(9): Show |
intron_variant | MODIFIER | c.2518+153G>C | FN1 | ENSG00000115414.21 | transcript | ENST00000354785.11 | protein_coding | 17/45 | chr2 | 215407955 | ||||||
chr2:215407956
|
A | C | 12 | a0001c0002t0001g0133a0001c0002t0001g0134a0001c0002t0001g0135others(9): Show | 12 | HG01109.hp2 HG01884.hp1 HG02145.hp1 others(9): Show |
intron_variant | MODIFIER | c.2518+152T>G | FN1 | ENSG00000115414.21 | transcript | ENST00000354785.11 | protein_coding | 17/45 | chr2 | 215407956 | ||||||
chr2:215408046
|
G | A | 15 | a0001c0002t0001g0133a0001c0002t0001g0134a0001c0002t0001g0135others(12): Show | 15 | HG01109.hp2 HG01884.hp1 HG01891.hp2 others(12): Show |
intron_variant | MODIFIER | c.2518+62C>T | FN1 | ENSG00000115414.21 | transcript | ENST00000354785.11 | protein_coding | 17/45 | chr2 | 215408046 | ||||||
chr2:215408096
|
C | G | 159 | a0001c0001t0001g0002a0001c0001t0001g0062a0001c0001t0001g0149others(156): Show | 160 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(157): Show |
intron_variant | MODIFIER | c.2518+12G>C | FN1 | ENSG00000115414.21 | transcript | ENST00000354785.11 | protein_coding | 17/45 | chr2 | 215408096 | ||||||
chr2:215408221
|
A | G | 1 | a0001c0025t0001g0163 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.2429-24T>C | FN1 | ENSG00000115414.21 | transcript | ENST00000354785.11 | protein_coding | 16/45 | chr2 | 215408221 | ||||||
chr2:215408261
|
A | G | 1 | a0002c0013t0001g0022 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.2428+37T>C | FN1 | ENSG00000115414.21 | transcript | ENST00000354785.11 | protein_coding | 16/45 | chr2 | 215408261 | ||||||
chr2:215408282
|
T | C | 1 | a0003c0048t0002g0100 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.2428+16A>G | FN1 | ENSG00000115414.21 | transcript | ENST00000354785.11 | protein_coding | 16/45 | chr2 | 215408282 | ||||||
chr2:215408479
|
G | A | 8 | a0002c0003t0001g0013a0002c0003t0001g0016a0002c0003t0001g0024others(5): Show | 8 | HG00639.hp1 HG01070.hp2 HG01071.hp1 others(5): Show |
intron_variant | MODIFIER | c.2300-53C>T | FN1 | ENSG00000115414.21 | transcript | ENST00000354785.11 | protein_coding | 15/45 | chr2 | 215408479 | ||||||
chr2:215408489
|
C | A | 1 | a0001c0012t0001g0081 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.2300-63G>T | FN1 | ENSG00000115414.21 | transcript | ENST00000354785.11 | protein_coding | 15/45 | chr2 | 215408489 | ||||||
chr2:215408702
|
G | A | 1 | a0002c0003t0001g0019 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.2300-276C>T | FN1 | ENSG00000115414.21 | transcript | ENST00000354785.11 | protein_coding | 15/45 | chr2 | 215408702 | ||||||
chr2:215408729
|
G | A | 56 | a0001c0002t0001g0111a0001c0002t0001g0112a0001c0002t0001g0113others(53): Show | 56 | HG00140.hp2 HG00323.hp2 HG00642.hp2 others(53): Show |
intron_variant | MODIFIER | c.2300-303C>T | FN1 | ENSG00000115414.21 | transcript | ENST00000354785.11 | protein_coding | 15/45 | chr2 | 215408729 | ||||||
chr2:215408796
|
C | T | 3 | a0002c0023t0001g0049a0002c0023t0001g0051a0018c0038t0002g0050 | 3 | HG01891.hp2 HG02257.hp2 HG02559.hp1 |
intron_variant | MODIFIER | c.2300-370G>A | FN1 | ENSG00000115414.21 | transcript | ENST00000354785.11 | protein_coding | 15/45 | chr2 | 215408796 | ||||||
chr2:215408860
|
G | A | 1 | a0016c0043t0001g0168 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.2300-434C>T | FN1 | ENSG00000115414.21 | transcript | ENST00000354785.11 | protein_coding | 15/45 | chr2 | 215408860 | ||||||
chr2:215408902
|
A | C | 64 | a0001c0002t0001g0133a0001c0002t0001g0134a0001c0002t0001g0135others(61): Show | 65 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(62): Show |
intron_variant | MODIFIER | c.2300-476T>G | FN1 | ENSG00000115414.21 | transcript | ENST00000354785.11 | protein_coding | 15/45 | chr2 | 215408902 | ||||||
chr2:215409006
|
T | A | 1 | a0015c0053t0001g0201 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.2299+557A>T | FN1 | ENSG00000115414.21 | transcript | ENST00000354785.11 | protein_coding | 15/45 | chr2 | 215409006 | ||||||
chr2:215409088
|
C | T | 215 | a0001c0001t0001g0002a0001c0001t0001g0062a0001c0001t0001g0149others(212): Show | 217 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(214): Show |
intron_variant | MODIFIER | c.2299+475G>A | FN1 | ENSG00000115414.21 | transcript | ENST00000354785.11 | protein_coding | 15/45 | chr2 | 215409088 | ||||||
chr2:215409216
|
A | G | 15 | a0001c0002t0001g0133a0001c0002t0001g0134a0001c0002t0001g0135others(12): Show | 15 | HG01109.hp2 HG01884.hp1 HG01891.hp2 others(12): Show |
intron_variant | MODIFIER | c.2299+347T>C | FN1 | ENSG00000115414.21 | transcript | ENST00000354785.11 | protein_coding | 15/45 | chr2 | 215409216 | ||||||
chr2:215409354
|
G | A | 3 | a0001c0012t0001g0154a0004c0020t0002g0005a0004c0020t0002g0006 | 3 | HG02970.hp1 NA18522.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.2299+209C>T | FN1 | ENSG00000115414.21 | transcript | ENST00000354785.11 | protein_coding | 15/45 | chr2 | 215409354 | ||||||
chr2:215409384
|
G | A | 1 | a0001c0042t0001g0148 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.2299+179C>T | FN1 | ENSG00000115414.21 | transcript | ENST00000354785.11 | protein_coding | 15/45 | chr2 | 215409384 | ||||||
chr2:215410130
|
A | AAC | 53 | a0001c0004t0001g0001a0001c0004t0001g0068a0001c0004t0001g0070others(50): Show | 54 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(51): Show |
intron_variant | MODIFIER | c.1942-18_1942-17dup others(2): Show |
FN1 | ENSG00000115414.21 | transcript | ENST00000354785.11 | protein_coding | 13/45 | chr2 | 215410130 | ||||||
chr2:215410130
|
A | AACAC | 18 | a0001c0002t0001g0133a0001c0002t0001g0134a0001c0002t0001g0137others(15): Show | 18 | HG01167.hp2 HG01261.hp2 HG01884.hp1 others(15): Show |
intron_variant | MODIFIER | c.1942-20_1942-17dup others(4): Show |
FN1 | ENSG00000115414.21 | transcript | ENST00000354785.11 | protein_coding | 13/45 | chr2 | 215410130 | ||||||
chr2:215410130
|
AAC | A | 78 | a0001c0001t0001g0002a0001c0001t0001g0062a0001c0001t0001g0149others(75): Show | 79 | HG00099.hp2 HG00280.hp2 HG00609.hp1 others(76): Show |
intron_variant | MODIFIER | c.1942-18_1942-17del others(2): Show |
FN1 | ENSG00000115414.21 | transcript | ENST00000354785.11 | protein_coding | 13/45 | chr2 | 215410130 | ||||||
chr2:215410220
|
A | G | 1 | a0002c0003t0001g0026 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.1942-106T>C | FN1 | ENSG00000115414.21 | transcript | ENST00000354785.11 | protein_coding | 13/45 | chr2 | 215410220 | ||||||
chr2:215410295
|
A | G | 1 | a0001c0001t0001g0169 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.1942-181T>C | FN1 | ENSG00000115414.21 | transcript | ENST00000354785.11 | protein_coding | 13/45 | chr2 | 215410295 | ||||||
chr2:215410473
|
G | A | 8 | a0001c0001t0001g0200a0001c0006t0001g0069a0001c0006t0001g0072others(5): Show | 8 | HG00140.hp1 HG01099.hp1 HG02273.hp1 others(5): Show |
intron_variant | MODIFIER | c.1942-359C>T | FN1 | ENSG00000115414.21 | transcript | ENST00000354785.11 | protein_coding | 13/45 | chr2 | 215410473 | ||||||
chr2:215410477
|
TGA | T | 7 | a0001c0009t0001g0155a0001c0009t0001g0157a0001c0046t0001g0164others(4): Show | 7 | HG02055.hp2 HG02559.hp2 HG02630.hp1 others(4): Show |
intron_variant | MODIFIER | c.1942-365_1942-364d others(4): Show |
FN1 | ENSG00000115414.21 | transcript | ENST00000354785.11 | protein_coding | 13/45 | chr2 | 215410477 | ||||||
chr2:215410496
|
G | A | 78 | a0001c0001t0001g0002a0001c0001t0001g0062a0001c0001t0001g0149others(75): Show | 79 | HG00099.hp2 HG00280.hp2 HG00609.hp1 others(76): Show |
intron_variant | MODIFIER | c.1942-382C>T | FN1 | ENSG00000115414.21 | transcript | ENST00000354785.11 | protein_coding | 13/45 | chr2 | 215410496 | ||||||
chr2:215410507
|
CT | C | 178 | a0001c0001t0001g0002a0001c0001t0001g0062a0001c0001t0001g0149others(175): Show | 180 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(177): Show |
intron_variant | MODIFIER | c.1942-394delA | FN1 | ENSG00000115414.21 | transcript | ENST00000354785.11 | protein_coding | 13/45 | chr2 | 215410507 | ||||||
chr2:215410517
|
T | A | 1 | a0015c0053t0001g0201 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.1942-403A>T | FN1 | ENSG00000115414.21 | transcript | ENST00000354785.11 | protein_coding | 13/45 | chr2 | 215410517 | ||||||
chr2:215410527
|
G | T | 16 | a0001c0002t0001g0133a0001c0002t0001g0134a0001c0002t0001g0135others(13): Show | 16 | HG01109.hp2 HG01884.hp1 HG01891.hp2 others(13): Show |
intron_variant | MODIFIER | c.1942-413C>A | FN1 | ENSG00000115414.21 | transcript | ENST00000354785.11 | protein_coding | 13/45 | chr2 | 215410527 | ||||||
chr2:215410537
|
T | C | 159 | a0001c0001t0001g0002a0001c0001t0001g0062a0001c0001t0001g0149others(156): Show | 161 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(158): Show |
intron_variant | MODIFIER | c.1942-423A>G | FN1 | ENSG00000115414.21 | transcript | ENST00000354785.11 | protein_coding | 13/45 | chr2 | 215410537 | ||||||
chr2:215410687
|
A | G | 1 | a0002c0013t0001g0022 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.1942-573T>C | FN1 | ENSG00000115414.21 | transcript | ENST00000354785.11 | protein_coding | 13/45 | chr2 | 215410687 | ||||||
chr2:215411048
|
G | A | 70 | a0001c0002t0001g0133a0001c0002t0001g0134a0001c0002t0001g0135others(67): Show | 71 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(68): Show |
intron_variant | MODIFIER | c.1942-934C>T | FN1 | ENSG00000115414.21 | transcript | ENST00000354785.11 | protein_coding | 13/45 | chr2 | 215411048 | ||||||
chr2:215411319
|
G | A | 159 | a0001c0001t0001g0002a0001c0001t0001g0062a0001c0001t0001g0149others(156): Show | 161 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(158): Show |
intron_variant | MODIFIER | c.1942-1205C>T | FN1 | ENSG00000115414.21 | transcript | ENST00000354785.11 | protein_coding | 13/45 | chr2 | 215411319 | ||||||
chr2:215411406
|
C | T | 8 | a0001c0015t0001g0101a0001c0015t0001g0102a0001c0015t0001g0103others(5): Show | 8 | HG02572.hp1 HG02622.hp2 HG02886.hp1 others(5): Show |
intron_variant | MODIFIER | c.1942-1292G>A | FN1 | ENSG00000115414.21 | transcript | ENST00000354785.11 | protein_coding | 13/45 | chr2 | 215411406 | ||||||
chr2:215411472
|
C | T | 4 | a0001c0015t0001g0101a0001c0015t0001g0102a0001c0015t0001g0103others(1): Show | 4 | HG02622.hp2 HG02896.hp2 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.1942-1358G>A | FN1 | ENSG00000115414.21 | transcript | ENST00000354785.11 | protein_coding | 13/45 | chr2 | 215411472 | ||||||
chr2:215411631
|
C | G | 5 | a0001c0012t0001g0154a0004c0019t0001g0004a0004c0019t0001g0007others(2): Show | 5 | HG02647.hp1 HG02922.hp2 HG02970.hp1 others(2): Show |
intron_variant | MODIFIER | c.1942-1517G>C | FN1 | ENSG00000115414.21 | transcript | ENST00000354785.11 | protein_coding | 13/45 | chr2 | 215411631 | ||||||
chr2:215411652
|
C | T | 78 | a0001c0001t0001g0002a0001c0001t0001g0062a0001c0001t0001g0149others(75): Show | 79 | HG00099.hp2 HG00280.hp2 HG00609.hp1 others(76): Show |
intron_variant | MODIFIER | c.1942-1538G>A | FN1 | ENSG00000115414.21 | transcript | ENST00000354785.11 | protein_coding | 13/45 | chr2 | 215411652 | ||||||
chr2:215411665
|
C | CT | 15 | a0001c0002t0001g0113a0001c0011t0001g0106a0001c0011t0001g0107others(12): Show | 15 | HG01168.hp1 HG01243.hp2 HG01346.hp1 others(12): Show |
intron_variant | MODIFIER | c.1942-1552dupA | FN1 | ENSG00000115414.21 | transcript | ENST00000354785.11 | protein_coding | 13/45 | chr2 | 215411665 | ||||||
chr2:215411665
|
CT | C | 126 | a0001c0001t0001g0002a0001c0001t0001g0062a0001c0001t0001g0149others(123): Show | 128 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(125): Show |
intron_variant | MODIFIER | c.1942-1552delA | FN1 | ENSG00000115414.21 | transcript | ENST00000354785.11 | protein_coding | 13/45 | chr2 | 215411665 | ||||||
chr2:215411665
|
CTT | C | 7 | a0001c0005t0001g0067a0001c0005t0001g0229a0002c0023t0001g0049others(4): Show | 7 | HG01891.hp2 HG02257.hp2 HG02559.hp1 others(4): Show |
intron_variant | MODIFIER | c.1942-1553_1942-155 others(6): Show |
FN1 | ENSG00000115414.21 | transcript | ENST00000354785.11 | protein_coding | 13/45 | chr2 | 215411665 | ||||||
chr2:215411959
|
G | A | 1 | a0001c0006t0001g0110 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1942-1845C>T | FN1 | ENSG00000115414.21 | transcript | ENST00000354785.11 | protein_coding | 13/45 | chr2 | 215411959 | ||||||
chr2:215412133
|
A | T | 83 | a0001c0001t0001g0002a0001c0001t0001g0062a0001c0001t0001g0149others(80): Show | 84 | HG00099.hp2 HG00280.hp2 HG00609.hp1 others(81): Show |
intron_variant | MODIFIER | c.1942-2019T>A | FN1 | ENSG00000115414.21 | transcript | ENST00000354785.11 | protein_coding | 13/45 | chr2 | 215412133 | ||||||
chr2:215412142
|
A | G | 1 | a0002c0003t0001g0036 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.1942-2028T>C | FN1 | ENSG00000115414.21 | transcript | ENST00000354785.11 | protein_coding | 13/45 | chr2 | 215412142 | ||||||
chr2:215412191
|
CT | C | 155 | a0001c0001t0001g0002a0001c0001t0001g0062a0001c0001t0001g0149others(152): Show | 157 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(154): Show |
intron_variant | MODIFIER | c.1942-2078delA | FN1 | ENSG00000115414.21 | transcript | ENST00000354785.11 | protein_coding | 13/45 | chr2 | 215412191 | ||||||
chr2:215412268
|
T | C | 54 | a0001c0004t0001g0001a0001c0004t0001g0068a0001c0004t0001g0070others(51): Show | 55 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(52): Show |
intron_variant | MODIFIER | c.1942-2154A>G | FN1 | ENSG00000115414.21 | transcript | ENST00000354785.11 | protein_coding | 13/45 | chr2 | 215412268 | ||||||
chr2:215412407
|
A | G | 86 | a0001c0001t0001g0002a0001c0001t0001g0062a0001c0001t0001g0149others(83): Show | 87 | HG00099.hp2 HG00280.hp2 HG00609.hp1 others(84): Show |
intron_variant | MODIFIER | c.1942-2293T>C | FN1 | ENSG00000115414.21 | transcript | ENST00000354785.11 | protein_coding | 13/45 | chr2 | 215412407 | ||||||
chr2:215412408
|
G | C | 86 | a0001c0001t0001g0002a0001c0001t0001g0062a0001c0001t0001g0149others(83): Show | 87 | HG00099.hp2 HG00280.hp2 HG00609.hp1 others(84): Show |
intron_variant | MODIFIER | c.1942-2294C>G | FN1 | ENSG00000115414.21 | transcript | ENST00000354785.11 | protein_coding | 13/45 | chr2 | 215412408 | ||||||
chr2:215412522
|
C | T | 1 | a0003c0007t0001g0160 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.1941+2315G>A | FN1 | ENSG00000115414.21 | transcript | ENST00000354785.11 | protein_coding | 13/45 | chr2 | 215412522 | ||||||
chr2:215412560
|
C | T | 1 | a0001c0050t0001g0182 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.1941+2277G>A | FN1 | ENSG00000115414.21 | transcript | ENST00000354785.11 | protein_coding | 13/45 | chr2 | 215412560 | ||||||
chr2:215412752
|
T | C | 1 | a0001c0042t0001g0148 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1941+2085A>G | FN1 | ENSG00000115414.21 | transcript | ENST00000354785.11 | protein_coding | 13/45 | chr2 | 215412752 | ||||||
chr2:215412760
|
C | CT | 56 | a0001c0002t0001g0135a0001c0004t0001g0001a0001c0004t0001g0068others(53): Show | 57 | HG00099.hp1 HG00323.hp1 HG00639.hp1 others(54): Show |
intron_variant | MODIFIER | c.1941+2076dupA | FN1 | ENSG00000115414.21 | transcript | ENST00000354785.11 | protein_coding | 13/45 | chr2 | 215412760 | ||||||
chr2:215412760
|
C | CTT | 13 | a0001c0004t0001g0070a0001c0004t0001g0071a0001c0004t0001g0080others(10): Show | 13 | HG00280.hp1 HG00741.hp1 HG01069.hp2 others(10): Show |
intron_variant | MODIFIER | c.1941+2075_1941+207 others(6): Show |
FN1 | ENSG00000115414.21 | transcript | ENST00000354785.11 | protein_coding | 13/45 | chr2 | 215412760 | ||||||
chr2:215412760
|
C | CTTTTTT | 6 | a0001c0004t0001g0087a0001c0011t0001g0106a0001c0011t0001g0107others(3): Show | 6 | HG01346.hp1 HG01515.hp2 HG02602.hp2 others(3): Show |
intron_variant | MODIFIER | c.1941+2071_1941+207 others(10): Show |
FN1 | ENSG00000115414.21 | transcript | ENST00000354785.11 | protein_coding | 13/45 | chr2 | 215412760 | ||||||
chr2:215412760
|
C | CTTTTTTT | 31 | a0001c0002t0001g0113a0001c0002t0001g0114a0001c0002t0001g0119others(28): Show | 31 | HG00140.hp2 HG00323.hp2 HG00642.hp2 others(28): Show |
intron_variant | MODIFIER | c.1941+2070_1941+207 others(11): Show |
FN1 | ENSG00000115414.21 | transcript | ENST00000354785.11 | protein_coding | 13/45 | chr2 | 215412760 | ||||||
chr2:215412760
|
C | CTTTTTTT others(1): Show |
11 | a0001c0002t0001g0111a0001c0002t0001g0112a0001c0002t0001g0131others(8): Show | 11 | HG01243.hp1 HG02280.hp1 HG02647.hp1 others(8): Show |
intron_variant | MODIFIER | c.1941+2069_1941+207 others(12): Show |
FN1 | ENSG00000115414.21 | transcript | ENST00000354785.11 | protein_coding | 13/45 | chr2 | 215412760 | ||||||
chr2:215412760
|
CT | C | 5 | a0001c0015t0001g0103a0001c0044t0001g0065a0007c0017t0001g0076others(2): Show | 5 | HG02258.hp2 HG02273.hp1 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.1941+2076delA | FN1 | ENSG00000115414.21 | transcript | ENST00000354785.11 | protein_coding | 13/45 | chr2 | 215412760 | ||||||
chr2:215412760
|
CTTTTTT | C | 79 | a0001c0001t0001g0002a0001c0001t0001g0062a0001c0001t0001g0149others(76): Show | 80 | HG00099.hp2 HG00280.hp2 HG00609.hp1 others(77): Show |
intron_variant | MODIFIER | c.1941+2071_1941+207 others(10): Show |
FN1 | ENSG00000115414.21 | transcript | ENST00000354785.11 | protein_coding | 13/45 | chr2 | 215412760 | ||||||
chr2:215412949
|
C | T | 84 | a0001c0001t0001g0002a0001c0001t0001g0062a0001c0001t0001g0149others(81): Show | 85 | HG00099.hp2 HG00280.hp2 HG00609.hp1 others(82): Show |
intron_variant | MODIFIER | c.1941+1888G>A | FN1 | ENSG00000115414.21 | transcript | ENST00000354785.11 | protein_coding | 13/45 | chr2 | 215412949 | ||||||
chr2:215413064
|
T | C | 7 | a0001c0009t0001g0155a0001c0009t0001g0157a0001c0012t0001g0154others(4): Show | 7 | HG02559.hp2 HG02630.hp1 HG02717.hp1 others(4): Show |
intron_variant | MODIFIER | c.1941+1773A>G | FN1 | ENSG00000115414.21 | transcript | ENST00000354785.11 | protein_coding | 13/45 | chr2 | 215413064 | ||||||
chr2:215413177
|
C | T | 9 | a0001c0011t0001g0106a0001c0011t0001g0107a0001c0011t0001g0108others(6): Show | 9 | HG01168.hp1 HG01346.hp1 HG01515.hp2 others(6): Show |
intron_variant | MODIFIER | c.1941+1660G>A | FN1 | ENSG00000115414.21 | transcript | ENST00000354785.11 | protein_coding | 13/45 | chr2 | 215413177 | ||||||
chr2:215413200
|
A | C | 143 | a0001c0001t0001g0002a0001c0001t0001g0062a0001c0001t0001g0149others(140): Show | 145 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(142): Show |
intron_variant | MODIFIER | c.1941+1637T>G | FN1 | ENSG00000115414.21 | transcript | ENST00000354785.11 | protein_coding | 13/45 | chr2 | 215413200 | ||||||
chr2:215413338
|
C | T | 9 | a0001c0011t0001g0106a0001c0011t0001g0107a0001c0011t0001g0108others(6): Show | 9 | HG01168.hp1 HG01346.hp1 HG01515.hp2 others(6): Show |
intron_variant | MODIFIER | c.1941+1499G>A | FN1 | ENSG00000115414.21 | transcript | ENST00000354785.11 | protein_coding | 13/45 | chr2 | 215413338 | ||||||
chr2:215413448
|
C | T | 2 | a0001c0041t0001g0147a0001c0042t0001g0148 | 2 | HG03540.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.1941+1389G>A | FN1 | ENSG00000115414.21 | transcript | ENST00000354785.11 | protein_coding | 13/45 | chr2 | 215413448 | ||||||
chr2:215413772
|
A | C | 53 | a0001c0004t0001g0001a0001c0004t0001g0068a0001c0004t0001g0070others(50): Show | 54 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(51): Show |
intron_variant | MODIFIER | c.1941+1065T>G | FN1 | ENSG00000115414.21 | transcript | ENST00000354785.11 | protein_coding | 13/45 | chr2 | 215413772 | ||||||
chr2:215413838
|
T | C | 1 | a0001c0001t0001g0202 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.1941+999A>G | FN1 | ENSG00000115414.21 | transcript | ENST00000354785.11 | protein_coding | 13/45 | chr2 | 215413838 | ||||||
chr2:215413930
|
CTA | C | 3 | a0001c0009t0001g0166a0001c0009t0002g0167a0001c0045t0001g0165 | 3 | HG02647.hp2 HG02723.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.1941+905_1941+906d others(4): Show |
FN1 | ENSG00000115414.21 | transcript | ENST00000354785.11 | protein_coding | 13/45 | chr2 | 215413930 | ||||||
chr2:215413933
|
G | A | 3 | a0001c0009t0001g0166a0001c0009t0002g0167a0001c0045t0001g0165 | 3 | HG02647.hp2 HG02723.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.1941+904C>T | FN1 | ENSG00000115414.21 | transcript | ENST00000354785.11 | protein_coding | 13/45 | chr2 | 215413933 | ||||||
chr2:215414069
|
C | G | 2 | a0001c0041t0001g0147a0001c0042t0001g0148 | 2 | HG03540.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.1941+768G>C | FN1 | ENSG00000115414.21 | transcript | ENST00000354785.11 | protein_coding | 13/45 | chr2 | 215414069 | ||||||
chr2:215414131
|
A | C | 1 | a0002c0003t0001g0024 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.1941+706T>G | FN1 | ENSG00000115414.21 | transcript | ENST00000354785.11 | protein_coding | 13/45 | chr2 | 215414131 | ||||||
chr2:215414360
|
T | A | 10 | a0001c0005t0001g0067a0001c0009t0001g0155a0001c0009t0001g0157others(7): Show | 10 | HG02559.hp2 HG02630.hp1 HG02717.hp1 others(7): Show |
intron_variant | MODIFIER | c.1941+477A>T | FN1 | ENSG00000115414.21 | transcript | ENST00000354785.11 | protein_coding | 13/45 | chr2 | 215414360 | ||||||
chr2:215414410
|
A | G | 2 | a0001c0025t0001g0163a0001c0046t0001g0164 | 2 | HG02055.hp2 HG02723.hp1 |
intron_variant | MODIFIER | c.1941+427T>C | FN1 | ENSG00000115414.21 | transcript | ENST00000354785.11 | protein_coding | 13/45 | chr2 | 215414410 | ||||||
chr2:215414419
|
A | C | 2 | a0001c0041t0001g0147a0001c0042t0001g0148 | 2 | HG03540.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.1941+418T>G | FN1 | ENSG00000115414.21 | transcript | ENST00000354785.11 | protein_coding | 13/45 | chr2 | 215414419 | ||||||
chr2:215414550
|
A | G | 6 | a0001c0004t0001g0087a0001c0011t0001g0106a0001c0011t0001g0107others(3): Show | 6 | HG01168.hp1 HG01346.hp1 HG01515.hp2 others(3): Show |
intron_variant | MODIFIER | c.1941+287T>C | FN1 | ENSG00000115414.21 | transcript | ENST00000354785.11 | protein_coding | 13/45 | chr2 | 215414550 | ||||||
chr2:215414622
|
C | T | 1 | a0001c0059t0001g0219 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.1941+215G>A | FN1 | ENSG00000115414.21 | transcript | ENST00000354785.11 | protein_coding | 13/45 | chr2 | 215414622 | ||||||
chr2:215415018
|
T | C | 2 | a0001c0041t0001g0147a0001c0042t0001g0148 | 2 | HG03540.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.1820-60A>G | FN1 | ENSG00000115414.21 | transcript | ENST00000354785.11 | protein_coding | 12/45 | chr2 | 215415018 | ||||||
chr2:215415019
|
G | A | 2 | a0001c0041t0001g0147a0001c0042t0001g0148 | 2 | HG03540.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.1820-61C>T | FN1 | ENSG00000115414.21 | transcript | ENST00000354785.11 | protein_coding | 12/45 | chr2 | 215415019 | ||||||
chr2:215415074
|
T | C | 5 | a0005c0029t0003g0234a0005c0029t0003g0235a0005c0065t0001g0236others(2): Show | 5 | HG02886.hp1 HG02970.hp2 HG03225.hp1 others(2): Show |
intron_variant | MODIFIER | c.1820-116A>G | FN1 | ENSG00000115414.21 | transcript | ENST00000354785.11 | protein_coding | 12/45 | chr2 | 215415074 | ||||||
chr2:215415112
|
G | A | 1 | a0002c0003t0001g0036 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.1820-154C>T | FN1 | ENSG00000115414.21 | transcript | ENST00000354785.11 | protein_coding | 12/45 | chr2 | 215415112 | ||||||
chr2:215415213
|
A | T | 68 | a0001c0002t0001g0111a0001c0002t0001g0112a0001c0002t0001g0113others(65): Show | 68 | HG00140.hp2 HG00323.hp2 HG00642.hp2 others(65): Show |
intron_variant | MODIFIER | c.1820-255T>A | FN1 | ENSG00000115414.21 | transcript | ENST00000354785.11 | protein_coding | 12/45 | chr2 | 215415213 | ||||||
chr2:215415225
|
CTT | C | 92 | a0001c0001t0001g0002a0001c0001t0001g0062a0001c0001t0001g0149others(89): Show | 93 | HG00099.hp2 HG00280.hp2 HG00609.hp1 others(90): Show |
intron_variant | MODIFIER | c.1820-269_1820-268d others(4): Show |
FN1 | ENSG00000115414.21 | transcript | ENST00000354785.11 | protein_coding | 12/45 | chr2 | 215415225 | ||||||
chr2:215415283
|
C | T | 6 | a0001c0004t0001g0087a0001c0011t0001g0106a0001c0011t0001g0107others(3): Show | 6 | HG01168.hp1 HG01346.hp1 HG01515.hp2 others(3): Show |
intron_variant | MODIFIER | c.1820-325G>A | FN1 | ENSG00000115414.21 | transcript | ENST00000354785.11 | protein_coding | 12/45 | chr2 | 215415283 | ||||||
chr2:215415742
|
T | C | 1 | a0002c0003t0001g0037 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.1820-784A>G | FN1 | ENSG00000115414.21 | transcript | ENST00000354785.11 | protein_coding | 12/45 | chr2 | 215415742 | ||||||
chr2:215415747
|
T | G | 4 | a0001c0015t0001g0101a0001c0015t0001g0102a0001c0015t0001g0103others(1): Show | 4 | HG02622.hp2 HG02896.hp2 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.1820-789A>C | FN1 | ENSG00000115414.21 | transcript | ENST00000354785.11 | protein_coding | 12/45 | chr2 | 215415747 | ||||||
chr2:215415793
|
A | C | 1 | a0001c0002t0001g0131 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.1820-835T>G | FN1 | ENSG00000115414.21 | transcript | ENST00000354785.11 | protein_coding | 12/45 | chr2 | 215415793 | ||||||
chr2:215415799
|
T | A | 52 | a0001c0004t0001g0001a0001c0004t0001g0068a0001c0004t0001g0070others(49): Show | 53 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(50): Show |
intron_variant | MODIFIER | c.1820-841A>T | FN1 | ENSG00000115414.21 | transcript | ENST00000354785.11 | protein_coding | 12/45 | chr2 | 215415799 | ||||||
chr2:215415850
|
T | C | 52 | a0001c0002t0001g0111a0001c0002t0001g0112a0001c0002t0001g0113others(49): Show | 52 | HG00140.hp2 HG00323.hp2 HG00642.hp2 others(49): Show |
intron_variant | MODIFIER | c.1820-892A>G | FN1 | ENSG00000115414.21 | transcript | ENST00000354785.11 | protein_coding | 12/45 | chr2 | 215415850 | ||||||
chr2:215415998
|
T | C | 200 | a0001c0001t0001g0002a0001c0001t0001g0062a0001c0001t0001g0149others(197): Show | 202 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(199): Show |
intron_variant | MODIFIER | c.1820-1040A>G | FN1 | ENSG00000115414.21 | transcript | ENST00000354785.11 | protein_coding | 12/45 | chr2 | 215415998 | ||||||
chr2:215416154
|
G | T | 46 | a0001c0002t0001g0111a0001c0002t0001g0112a0001c0002t0001g0113others(43): Show | 46 | HG00140.hp2 HG00323.hp2 HG00642.hp2 others(43): Show |
intron_variant | MODIFIER | c.1820-1196C>A | FN1 | ENSG00000115414.21 | transcript | ENST00000354785.11 | protein_coding | 12/45 | chr2 | 215416154 | ||||||
chr2:215416280
|
C | T | 1 | a0001c0005t0001g0179 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.1820-1322G>A | FN1 | ENSG00000115414.21 | transcript | ENST00000354785.11 | protein_coding | 12/45 | chr2 | 215416280 | ||||||
chr2:215416332
|
T | C | 2 | a0001c0004t0001g0070a0001c0004t0001g0071 | 2 | HG02451.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.1820-1374A>G | FN1 | ENSG00000115414.21 | transcript | ENST00000354785.11 | protein_coding | 12/45 | chr2 | 215416332 | ||||||
chr2:215416392
|
C | A | 2 | a0001c0025t0001g0163a0001c0046t0001g0164 | 2 | HG02055.hp2 HG02723.hp1 |
intron_variant | MODIFIER | c.1820-1434G>T | FN1 | ENSG00000115414.21 | transcript | ENST00000354785.11 | protein_coding | 12/45 | chr2 | 215416392 | ||||||
chr2:215416399
|
T | C | 215 | a0001c0001t0001g0002a0001c0001t0001g0062a0001c0001t0001g0149others(212): Show | 217 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(214): Show |
intron_variant | MODIFIER | c.1820-1441A>G | FN1 | ENSG00000115414.21 | transcript | ENST00000354785.11 | protein_coding | 12/45 | chr2 | 215416399 | ||||||
chr2:215416639
|
C | T | 200 | a0001c0001t0001g0002a0001c0001t0001g0062a0001c0001t0001g0149others(197): Show | 202 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(199): Show |
intron_variant | MODIFIER | c.1820-1681G>A | FN1 | ENSG00000115414.21 | transcript | ENST00000354785.11 | protein_coding | 12/45 | chr2 | 215416639 | ||||||
chr2:215416691
|
A | T | 215 | a0001c0001t0001g0002a0001c0001t0001g0062a0001c0001t0001g0149others(212): Show | 217 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(214): Show |
intron_variant | MODIFIER | c.1820-1733T>A | FN1 | ENSG00000115414.21 | transcript | ENST00000354785.11 | protein_coding | 12/45 | chr2 | 215416691 | ||||||
chr2:215416896
|
C | G | 51 | a0001c0002t0001g0111a0001c0002t0001g0112a0001c0002t0001g0113others(48): Show | 51 | HG00140.hp2 HG00323.hp2 HG00642.hp2 others(48): Show |
intron_variant | MODIFIER | c.1820-1938G>C | FN1 | ENSG00000115414.21 | transcript | ENST00000354785.11 | protein_coding | 12/45 | chr2 | 215416896 | ||||||
chr2:215416907
|
G | C | 93 | a0001c0001t0001g0002a0001c0001t0001g0062a0001c0001t0001g0149others(90): Show | 94 | HG00099.hp2 HG00280.hp2 HG00609.hp1 others(91): Show |
intron_variant | MODIFIER | c.1820-1949C>G | FN1 | ENSG00000115414.21 | transcript | ENST00000354785.11 | protein_coding | 12/45 | chr2 | 215416907 | ||||||
chr2:215416975
|
C | CA | 200 | a0001c0001t0001g0002a0001c0001t0001g0062a0001c0001t0001g0149others(197): Show | 202 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(199): Show |
intron_variant | MODIFIER | c.1820-2018dupT | FN1 | ENSG00000115414.21 | transcript | ENST00000354785.11 | protein_coding | 12/45 | chr2 | 215416975 | ||||||
chr2:215417157
|
T | C | 1 | a0001c0001t0001g0203 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.1819+2085A>G | FN1 | ENSG00000115414.21 | transcript | ENST00000354785.11 | protein_coding | 12/45 | chr2 | 215417157 | ||||||
chr2:215417174
|
C | T | 1 | a0001c0058t0002g0153 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.1819+2068G>A | FN1 | ENSG00000115414.21 | transcript | ENST00000354785.11 | protein_coding | 12/45 | chr2 | 215417174 | ||||||
chr2:215417184
|
A | C | 5 | a0005c0029t0003g0234a0005c0029t0003g0235a0005c0065t0001g0236others(2): Show | 5 | HG02886.hp1 HG02970.hp2 HG03225.hp1 others(2): Show |
intron_variant | MODIFIER | c.1819+2058T>G | FN1 | ENSG00000115414.21 | transcript | ENST00000354785.11 | protein_coding | 12/45 | chr2 | 215417184 | ||||||
chr2:215417283
|
A | G | 1 | a0001c0012t0001g0154 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.1819+1959T>C | FN1 | ENSG00000115414.21 | transcript | ENST00000354785.11 | protein_coding | 12/45 | chr2 | 215417283 | ||||||
chr2:215417294
|
G | A | 46 | a0001c0002t0001g0111a0001c0002t0001g0112a0001c0002t0001g0113others(43): Show | 46 | HG00140.hp2 HG00323.hp2 HG00642.hp2 others(43): Show |
intron_variant | MODIFIER | c.1819+1948C>T | FN1 | ENSG00000115414.21 | transcript | ENST00000354785.11 | protein_coding | 12/45 | chr2 | 215417294 | ||||||
chr2:215417758
|
G | A | 53 | a0001c0004t0001g0001a0001c0004t0001g0068a0001c0004t0001g0070others(50): Show | 54 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(51): Show |
intron_variant | MODIFIER | c.1819+1484C>T | FN1 | ENSG00000115414.21 | transcript | ENST00000354785.11 | protein_coding | 12/45 | chr2 | 215417758 | ||||||
chr2:215417782
|
A | G | 1 | a0001c0005t0001g0178 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.1819+1460T>C | FN1 | ENSG00000115414.21 | transcript | ENST00000354785.11 | protein_coding | 12/45 | chr2 | 215417782 | ||||||
chr2:215417931
|
C | T | 1 | a0001c0051t0001g0207 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.1819+1311G>A | FN1 | ENSG00000115414.21 | transcript | ENST00000354785.11 | protein_coding | 12/45 | chr2 | 215417931 | ||||||
chr2:215417958
|
C | A | 51 | a0001c0002t0001g0111a0001c0002t0001g0112a0001c0002t0001g0113others(48): Show | 51 | HG00140.hp2 HG00323.hp2 HG00642.hp2 others(48): Show |
intron_variant | MODIFIER | c.1819+1284G>T | FN1 | ENSG00000115414.21 | transcript | ENST00000354785.11 | protein_coding | 12/45 | chr2 | 215417958 | ||||||
chr2:215418251
|
T | C | 53 | a0001c0004t0001g0001a0001c0004t0001g0068a0001c0004t0001g0070others(50): Show | 54 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(51): Show |
intron_variant | MODIFIER | c.1819+991A>G | FN1 | ENSG00000115414.21 | transcript | ENST00000354785.11 | protein_coding | 12/45 | chr2 | 215418251 | ||||||
chr2:215418270
|
T | C | 52 | a0001c0002t0001g0111a0001c0002t0001g0112a0001c0002t0001g0113others(49): Show | 52 | HG00140.hp2 HG00323.hp2 HG00642.hp2 others(49): Show |
intron_variant | MODIFIER | c.1819+972A>G | FN1 | ENSG00000115414.21 | transcript | ENST00000354785.11 | protein_coding | 12/45 | chr2 | 215418270 | ||||||
chr2:215418303
|
C | T | 1 | a0001c0001t0001g0177 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.1819+939G>A | FN1 | ENSG00000115414.21 | transcript | ENST00000354785.11 | protein_coding | 12/45 | chr2 | 215418303 | ||||||
chr2:215418316
|
G | T | 3 | a0001c0001t0001g0175a0001c0001t0001g0217a0001c0005t0001g0176 | 3 | HG01928.hp2 HG01978.hp2 HG02273.hp2 |
intron_variant | MODIFIER | c.1819+926C>A | FN1 | ENSG00000115414.21 | transcript | ENST00000354785.11 | protein_coding | 12/45 | chr2 | 215418316 | ||||||
chr2:215418372
|
C | T | 1 | a0001c0002t0001g0131 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.1819+870G>A | FN1 | ENSG00000115414.21 | transcript | ENST00000354785.11 | protein_coding | 12/45 | chr2 | 215418372 | ||||||
chr2:215418383
|
T | C | 215 | a0001c0001t0001g0002a0001c0001t0001g0062a0001c0001t0001g0149others(212): Show | 217 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(214): Show |
intron_variant | MODIFIER | c.1819+859A>G | FN1 | ENSG00000115414.21 | transcript | ENST00000354785.11 | protein_coding | 12/45 | chr2 | 215418383 | ||||||
chr2:215418484
|
C | T | 7 | a0001c0009t0001g0155a0001c0009t0001g0157a0001c0012t0001g0154others(4): Show | 7 | HG02559.hp2 HG02630.hp1 HG02717.hp1 others(4): Show |
intron_variant | MODIFIER | c.1819+758G>A | FN1 | ENSG00000115414.21 | transcript | ENST00000354785.11 | protein_coding | 12/45 | chr2 | 215418484 | ||||||
chr2:215418527
|
A | G | 1 | a0002c0003t0001g0042 | 1 | NA18975.hp1 | intron_variant | MODIFIER | c.1819+715T>C | FN1 | ENSG00000115414.21 | transcript | ENST00000354785.11 | protein_coding | 12/45 | chr2 | 215418527 | ||||||
chr2:215418613
|
C | T | 1 | a0001c0012t0001g0079 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.1819+629G>A | FN1 | ENSG00000115414.21 | transcript | ENST00000354785.11 | protein_coding | 12/45 | chr2 | 215418613 | ||||||
chr2:215418835
|
C | A | 85 | a0001c0001t0001g0002a0001c0001t0001g0062a0001c0001t0001g0149others(82): Show | 86 | HG00099.hp2 HG00280.hp2 HG00609.hp1 others(83): Show |
intron_variant | MODIFIER | c.1819+407G>T | FN1 | ENSG00000115414.21 | transcript | ENST00000354785.11 | protein_coding | 12/45 | chr2 | 215418835 | ||||||
chr2:215418971
|
CAG | C | 10 | a0001c0005t0001g0067a0001c0009t0001g0155a0001c0009t0001g0157others(7): Show | 10 | HG02559.hp2 HG02630.hp1 HG02717.hp1 others(7): Show |
intron_variant | MODIFIER | c.1819+269_1819+270d others(4): Show |
FN1 | ENSG00000115414.21 | transcript | ENST00000354785.11 | protein_coding | 12/45 | chr2 | 215418971 | ||||||
chr2:215419190
|
G | A | 1 | a0001c0002t0001g0144 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1819+52C>T | FN1 | ENSG00000115414.21 | transcript | ENST00000354785.11 | protein_coding | 12/45 | chr2 | 215419190 | ||||||
chr2:215419235
|
T | A | 90 | a0001c0001t0001g0002a0001c0001t0001g0062a0001c0001t0001g0149others(87): Show | 91 | HG00099.hp2 HG00280.hp2 HG00609.hp1 others(88): Show |
splice_region_variant&intron_variant | LOW | c.1819+7A>T | FN1 | ENSG00000115414.21 | transcript | ENST00000354785.11 | protein_coding | 12/45 | chr2 | 215419235 | ||||||
chr2:215419555
|
T | G | 2 | a0002c0014t0001g0056a0003c0007t0002g0066 | 2 | HG02818.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.1676-170A>C | FN1 | ENSG00000115414.21 | transcript | ENST00000354785.11 | protein_coding | 11/45 | chr2 | 215419555 | ||||||
chr2:215419561
|
TA | T | 88 | a0001c0001t0001g0002a0001c0001t0001g0062a0001c0001t0001g0149others(85): Show | 89 | HG00099.hp2 HG00280.hp2 HG00609.hp1 others(86): Show |
intron_variant | MODIFIER | c.1676-177delT | FN1 | ENSG00000115414.21 | transcript | ENST00000354785.11 | protein_coding | 11/45 | chr2 | 215419561 | ||||||
chr2:215419696
|
T | A | 1 | a0007c0017t0001g0076 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.1676-311A>T | FN1 | ENSG00000115414.21 | transcript | ENST00000354785.11 | protein_coding | 11/45 | chr2 | 215419696 | ||||||
chr2:215419712
|
T | C | 1 | a0002c0008t0001g0021 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.1676-327A>G | FN1 | ENSG00000115414.21 | transcript | ENST00000354785.11 | protein_coding | 11/45 | chr2 | 215419712 | ||||||
chr2:215419759
|
T | C | 6 | a0002c0003t0001g0042a0002c0003t0001g0044a0002c0003t0001g0045others(3): Show | 6 | HG02083.hp2 NA18943.hp2 NA18975.hp1 others(3): Show |
intron_variant | MODIFIER | c.1676-374A>G | FN1 | ENSG00000115414.21 | transcript | ENST00000354785.11 | protein_coding | 11/45 | chr2 | 215419759 | ||||||
chr2:215419921
|
G | C | 1 | a0001c0001t0001g0204 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.1676-536C>G | FN1 | ENSG00000115414.21 | transcript | ENST00000354785.11 | protein_coding | 11/45 | chr2 | 215419921 | ||||||
chr2:215419925
|
T | C | 4 | a0001c0015t0001g0101a0001c0015t0001g0102a0001c0015t0001g0103others(1): Show | 4 | HG02622.hp2 HG02896.hp2 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.1676-540A>G | FN1 | ENSG00000115414.21 | transcript | ENST00000354785.11 | protein_coding | 11/45 | chr2 | 215419925 | ||||||
chr2:215420051
|
C | T | 93 | a0001c0001t0001g0002a0001c0001t0001g0062a0001c0001t0001g0149others(90): Show | 94 | HG00099.hp2 HG00280.hp2 HG00609.hp1 others(91): Show |
intron_variant | MODIFIER | c.1675+622G>A | FN1 | ENSG00000115414.21 | transcript | ENST00000354785.11 | protein_coding | 11/45 | chr2 | 215420051 | ||||||
chr2:215420055
|
C | CA | 6 | a0001c0004t0001g0087a0001c0011t0001g0106a0001c0011t0001g0107others(3): Show | 6 | HG01168.hp1 HG01346.hp1 HG01515.hp2 others(3): Show |
intron_variant | MODIFIER | c.1675+617dupT | FN1 | ENSG00000115414.21 | transcript | ENST00000354785.11 | protein_coding | 11/45 | chr2 | 215420055 | ||||||
chr2:215420165
|
C | G | 1 | a0001c0002t0001g0135 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.1675+508G>C | FN1 | ENSG00000115414.21 | transcript | ENST00000354785.11 | protein_coding | 11/45 | chr2 | 215420165 | ||||||
chr2:215420254
|
G | C | 1 | a0001c0001t0001g0216 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.1675+419C>G | FN1 | ENSG00000115414.21 | transcript | ENST00000354785.11 | protein_coding | 11/45 | chr2 | 215420254 | ||||||
chr2:215420287
|
C | T | 2 | a0001c0025t0001g0163a0001c0046t0001g0164 | 2 | HG02055.hp2 HG02723.hp1 |
intron_variant | MODIFIER | c.1675+386G>A | FN1 | ENSG00000115414.21 | transcript | ENST00000354785.11 | protein_coding | 11/45 | chr2 | 215420287 | ||||||
chr2:215420310
|
C | T | 1 | a0001c0051t0001g0207 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.1675+363G>A | FN1 | ENSG00000115414.21 | transcript | ENST00000354785.11 | protein_coding | 11/45 | chr2 | 215420310 | ||||||
chr2:215420315
|
G | A | 53 | a0001c0004t0001g0001a0001c0004t0001g0068a0001c0004t0001g0070others(50): Show | 54 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(51): Show |
intron_variant | MODIFIER | c.1675+358C>T | FN1 | ENSG00000115414.21 | transcript | ENST00000354785.11 | protein_coding | 11/45 | chr2 | 215420315 | ||||||
chr2:215420340
|
AAAAAAC | A | 53 | a0001c0004t0001g0001a0001c0004t0001g0068a0001c0004t0001g0070others(50): Show | 54 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(51): Show |
intron_variant | MODIFIER | c.1675+327_1675+332d others(8): Show |
FN1 | ENSG00000115414.21 | transcript | ENST00000354785.11 | protein_coding | 11/45 | chr2 | 215420340 | ||||||
chr2:215420368
|
C | CA | 83 | a0001c0001t0001g0002a0001c0001t0001g0062a0001c0001t0001g0149others(80): Show | 84 | HG00099.hp2 HG00280.hp2 HG00609.hp1 others(81): Show |
intron_variant | MODIFIER | c.1675+304dupT | FN1 | ENSG00000115414.21 | transcript | ENST00000354785.11 | protein_coding | 11/45 | chr2 | 215420368 | ||||||
chr2:215420371
|
A | AC | 10 | a0001c0044t0001g0065a0004c0019t0001g0004a0004c0019t0001g0007others(7): Show | 10 | HG02258.hp2 HG02647.hp1 HG02886.hp1 others(7): Show |
intron_variant | MODIFIER | c.1675+301_1675+302i others(3): Show |
FN1 | ENSG00000115414.21 | transcript | ENST00000354785.11 | protein_coding | 11/45 | chr2 | 215420371 | ||||||
chr2:215420559
|
C | T | 1 | a0001c0006t0001g0072 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.1675+114G>A | FN1 | ENSG00000115414.21 | transcript | ENST00000354785.11 | protein_coding | 11/45 | chr2 | 215420559 | ||||||
chr2:215420638
|
T | C | 2 | a0001c0009t0001g0166a0001c0009t0002g0167 | 2 | HG02647.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.1675+35A>G | FN1 | ENSG00000115414.21 | transcript | ENST00000354785.11 | protein_coding | 11/45 | chr2 | 215420638 | ||||||
chr2:215420652
|
T | C | 6 | a0001c0004t0001g0087a0001c0011t0001g0106a0001c0011t0001g0107others(3): Show | 6 | HG01168.hp1 HG01346.hp1 HG01515.hp2 others(3): Show |
intron_variant | MODIFIER | c.1675+21A>G | FN1 | ENSG00000115414.21 | transcript | ENST00000354785.11 | protein_coding | 11/45 | chr2 | 215420652 | ||||||
chr2:215420807
|
T | C | 1 | a0001c0010t0001g0205 | 1 | HG02165.hp2 | splice_region_variant&intron_variant | LOW | c.1547-6A>G | FN1 | ENSG00000115414.21 | transcript | ENST00000354785.11 | protein_coding | 10/45 | chr2 | 215420807 | ||||||
chr2:215420906
|
A | G | 1 | a0001c0006t0001g0110 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1547-105T>C | FN1 | ENSG00000115414.21 | transcript | ENST00000354785.11 | protein_coding | 10/45 | chr2 | 215420906 | ||||||
chr2:215421006
|
C | T | 46 | a0001c0002t0001g0111a0001c0002t0001g0112a0001c0002t0001g0113others(43): Show | 46 | HG00140.hp2 HG00323.hp2 HG00642.hp2 others(43): Show |
intron_variant | MODIFIER | c.1547-205G>A | FN1 | ENSG00000115414.21 | transcript | ENST00000354785.11 | protein_coding | 10/45 | chr2 | 215421006 | ||||||
chr2:215421765
|
C | A | 2 | a0001c0041t0001g0147a0001c0042t0001g0148 | 2 | HG03540.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.1546+326G>T | FN1 | ENSG00000115414.21 | transcript | ENST00000354785.11 | protein_coding | 10/45 | chr2 | 215421765 | ||||||
chr2:215421806
|
T | G | 1 | a0001c0010t0001g0152 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.1546+285A>C | FN1 | ENSG00000115414.21 | transcript | ENST00000354785.11 | protein_coding | 10/45 | chr2 | 215421806 | ||||||
chr2:215422298
|
T | C | 1 | a0001c0010t0001g0230 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.1394-55A>G | FN1 | ENSG00000115414.21 | transcript | ENST00000354785.11 | protein_coding | 9/45 | chr2 | 215422298 | ||||||
chr2:215422370
|
A | G | 188 | a0001c0001t0001g0002a0001c0001t0001g0062a0001c0001t0001g0149others(185): Show | 190 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(187): Show |
intron_variant | MODIFIER | c.1394-127T>C | FN1 | ENSG00000115414.21 | transcript | ENST00000354785.11 | protein_coding | 9/45 | chr2 | 215422370 | ||||||
chr2:215422374
|
A | G | 45 | a0001c0002t0001g0111a0001c0002t0001g0112a0001c0002t0001g0113others(42): Show | 45 | HG00140.hp2 HG00323.hp2 HG00642.hp2 others(42): Show |
intron_variant | MODIFIER | c.1394-131T>C | FN1 | ENSG00000115414.21 | transcript | ENST00000354785.11 | protein_coding | 9/45 | chr2 | 215422374 | ||||||
chr2:215422476
|
G | C | 1 | a0003c0048t0002g0100 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.1394-233C>G | FN1 | ENSG00000115414.21 | transcript | ENST00000354785.11 | protein_coding | 9/45 | chr2 | 215422476 | ||||||
chr2:215422478
|
G | T | 1 | a0001c0058t0002g0153 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.1394-235C>A | FN1 | ENSG00000115414.21 | transcript | ENST00000354785.11 | protein_coding | 9/45 | chr2 | 215422478 | ||||||
chr2:215422511
|
C | T | 1 | a0001c0006t0001g0069 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.1394-268G>A | FN1 | ENSG00000115414.21 | transcript | ENST00000354785.11 | protein_coding | 9/45 | chr2 | 215422511 | ||||||
chr2:215422553
|
A | G | 82 | a0001c0001t0001g0002a0001c0001t0001g0062a0001c0001t0001g0149others(79): Show | 83 | HG00099.hp2 HG00280.hp2 HG00609.hp1 others(80): Show |
intron_variant | MODIFIER | c.1394-310T>C | FN1 | ENSG00000115414.21 | transcript | ENST00000354785.11 | protein_coding | 9/45 | chr2 | 215422553 | ||||||
chr2:215422774
|
A | G | 57 | a0001c0004t0001g0001a0001c0004t0001g0068a0001c0004t0001g0070others(54): Show | 58 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(55): Show |
intron_variant | MODIFIER | c.1394-531T>C | FN1 | ENSG00000115414.21 | transcript | ENST00000354785.11 | protein_coding | 9/45 | chr2 | 215422774 | ||||||
chr2:215422890
|
T | A | 1 | a0001c0001t0001g0206 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.1393+460A>T | FN1 | ENSG00000115414.21 | transcript | ENST00000354785.11 | protein_coding | 9/45 | chr2 | 215422890 | ||||||
chr2:215423067
|
G | C | 1 | a0001c0012t0001g0154 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.1393+283C>G | FN1 | ENSG00000115414.21 | transcript | ENST00000354785.11 | protein_coding | 9/45 | chr2 | 215423067 | ||||||
chr2:215423073
|
C | G | 36 | a0002c0003t0001g0013a0002c0003t0001g0016a0002c0003t0001g0019others(33): Show | 36 | HG00280.hp1 HG00639.hp1 HG00741.hp1 others(33): Show |
intron_variant | MODIFIER | c.1393+277G>C | FN1 | ENSG00000115414.21 | transcript | ENST00000354785.11 | protein_coding | 9/45 | chr2 | 215423073 | ||||||
chr2:215423168
|
T | G | 1 | a0002c0014t0001g0056 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.1393+182A>C | FN1 | ENSG00000115414.21 | transcript | ENST00000354785.11 | protein_coding | 9/45 | chr2 | 215423168 | ||||||
chr2:215423180
|
T | TCA | 44 | a0001c0002t0001g0111a0001c0002t0001g0112a0001c0002t0001g0113others(41): Show | 44 | HG00323.hp2 HG00738.hp1 HG00738.hp2 others(41): Show |
intron_variant | MODIFIER | c.1393+168_1393+169d others(4): Show |
FN1 | ENSG00000115414.21 | transcript | ENST00000354785.11 | protein_coding | 9/45 | chr2 | 215423180 | ||||||
chr2:215423180
|
T | TCACA | 26 | a0001c0002t0001g0129a0001c0004t0001g0070a0001c0004t0001g0071others(23): Show | 26 | HG00140.hp1 HG00140.hp2 HG01256.hp2 others(23): Show |
intron_variant | MODIFIER | c.1393+166_1393+169d others(6): Show |
FN1 | ENSG00000115414.21 | transcript | ENST00000354785.11 | protein_coding | 9/45 | chr2 | 215423180 | ||||||
chr2:215423180
|
T | TCACACA | 21 | a0001c0004t0001g0001a0001c0004t0001g0068a0001c0004t0001g0080others(18): Show | 22 | HG00099.hp1 HG00323.hp1 HG00735.hp2 others(19): Show |
intron_variant | MODIFIER | c.1393+164_1393+169d others(8): Show |
FN1 | ENSG00000115414.21 | transcript | ENST00000354785.11 | protein_coding | 9/45 | chr2 | 215423180 | ||||||
chr2:215423180
|
T | TCACACAC others(3): Show |
8 | a0001c0009t0001g0155a0001c0009t0001g0157a0001c0025t0001g0162others(5): Show | 8 | HG02055.hp2 HG02258.hp1 HG02559.hp2 others(5): Show |
intron_variant | MODIFIER | c.1393+160_1393+169d others(12): Show |
FN1 | ENSG00000115414.21 | transcript | ENST00000354785.11 | protein_coding | 9/45 | chr2 | 215423180 | ||||||
chr2:215423180
|
T | TCACACAC others(5): Show |
3 | a0001c0042t0001g0148a0003c0007t0001g0088a0003c0007t0001g0160 | 3 | HG02886.hp2 HG03098.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.1393+158_1393+169d others(14): Show |
FN1 | ENSG00000115414.21 | transcript | ENST00000354785.11 | protein_coding | 9/45 | chr2 | 215423180 | ||||||
chr2:215423180
|
T | TCACACAC others(7): Show |
1 | a0001c0005t0001g0067 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.1393+156_1393+169d others(16): Show |
FN1 | ENSG00000115414.21 | transcript | ENST00000354785.11 | protein_coding | 9/45 | chr2 | 215423180 | ||||||
chr2:215423180
|
TCA | T | 67 | a0001c0001t0001g0002a0001c0001t0001g0149a0001c0001t0001g0150others(64): Show | 68 | HG00609.hp1 HG00609.hp2 HG00642.hp1 others(65): Show |
intron_variant | MODIFIER | c.1393+168_1393+169d others(4): Show |
FN1 | ENSG00000115414.21 | transcript | ENST00000354785.11 | protein_coding | 9/45 | chr2 | 215423180 | ||||||
chr2:215423558
|
A | G | 1 | a0002c0003t0001g0019 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.1217-32T>C | FN1 | ENSG00000115414.21 | transcript | ENST00000354785.11 | protein_coding | 8/45 | chr2 | 215423558 | ||||||
chr2:215423749
|
A | AC | 74 | a0001c0001t0001g0002a0001c0001t0001g0062a0001c0001t0001g0149others(71): Show | 75 | HG00099.hp2 HG00280.hp2 HG00609.hp1 others(72): Show |
intron_variant | MODIFIER | c.1217-224dupG | FN1 | ENSG00000115414.21 | transcript | ENST00000354785.11 | protein_coding | 8/45 | chr2 | 215423749 | ||||||
chr2:215423757
|
C | A | 2 | a0001c0009t0001g0166a0001c0009t0002g0167 | 2 | HG02647.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.1217-231G>T | FN1 | ENSG00000115414.21 | transcript | ENST00000354785.11 | protein_coding | 8/45 | chr2 | 215423757 | ||||||
chr2:215423777
|
C | A | 1 | a0001c0045t0001g0165 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.1217-251G>T | FN1 | ENSG00000115414.21 | transcript | ENST00000354785.11 | protein_coding | 8/45 | chr2 | 215423777 | ||||||
chr2:215424038
|
G | A | 5 | a0005c0029t0003g0234a0005c0029t0003g0235a0005c0065t0001g0236others(2): Show | 5 | HG02886.hp1 HG02970.hp2 HG03225.hp1 others(2): Show |
intron_variant | MODIFIER | c.1216+108C>T | FN1 | ENSG00000115414.21 | transcript | ENST00000354785.11 | protein_coding | 8/45 | chr2 | 215424038 | ||||||
chr2:215424054
|
G | A | 2 | a0002c0003t0001g0039a0002c0003t0001g0040 | 2 | HG00741.hp2 HG01167.hp2 |
intron_variant | MODIFIER | c.1216+92C>T | FN1 | ENSG00000115414.21 | transcript | ENST00000354785.11 | protein_coding | 8/45 | chr2 | 215424054 | ||||||
chr2:215424072
|
G | A | 45 | a0001c0002t0001g0111a0001c0002t0001g0112a0001c0002t0001g0113others(42): Show | 45 | HG00140.hp2 HG00323.hp2 HG00642.hp2 others(42): Show |
intron_variant | MODIFIER | c.1216+74C>T | FN1 | ENSG00000115414.21 | transcript | ENST00000354785.11 | protein_coding | 8/45 | chr2 | 215424072 | ||||||
chr2:215424116
|
A | C | 17 | a0001c0006t0001g0110a0001c0009t0001g0155a0001c0009t0001g0157others(14): Show | 17 | HG02055.hp2 HG02109.hp2 HG02258.hp1 others(14): Show |
intron_variant | MODIFIER | c.1216+30T>G | FN1 | ENSG00000115414.21 | transcript | ENST00000354785.11 | protein_coding | 8/45 | chr2 | 215424116 | ||||||
chr2:215424118
|
T | C | 44 | a0001c0004t0001g0001a0001c0004t0001g0068a0001c0004t0001g0070others(41): Show | 45 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(42): Show |
intron_variant | MODIFIER | c.1216+28A>G | FN1 | ENSG00000115414.21 | transcript | ENST00000354785.11 | protein_coding | 8/45 | chr2 | 215424118 | ||||||
chr2:215424346
|
G | C | 5 | a0005c0029t0003g0234a0005c0029t0003g0235a0005c0065t0001g0236others(2): Show | 5 | HG02886.hp1 HG02970.hp2 HG03225.hp1 others(2): Show |
intron_variant | MODIFIER | c.1037-21C>G | FN1 | ENSG00000115414.21 | transcript | ENST00000354785.11 | protein_coding | 7/45 | chr2 | 215424346 | ||||||
chr2:215424510
|
T | A | 1 | a0002c0003t0001g0013 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.1037-185A>T | FN1 | ENSG00000115414.21 | transcript | ENST00000354785.11 | protein_coding | 7/45 | chr2 | 215424510 | ||||||
chr2:215424539
|
GTCCT | G | 45 | a0001c0002t0001g0111a0001c0002t0001g0112a0001c0002t0001g0113others(42): Show | 45 | HG00140.hp2 HG00323.hp2 HG00642.hp2 others(42): Show |
intron_variant | MODIFIER | c.1037-218_1037-215d others(6): Show |
FN1 | ENSG00000115414.21 | transcript | ENST00000354785.11 | protein_coding | 7/45 | chr2 | 215424539 | ||||||
chr2:215424620
|
G | A | 92 | a0001c0001t0001g0002a0001c0001t0001g0062a0001c0001t0001g0149others(89): Show | 93 | HG00099.hp2 HG00280.hp2 HG00609.hp1 others(90): Show |
intron_variant | MODIFIER | c.1037-295C>T | FN1 | ENSG00000115414.21 | transcript | ENST00000354785.11 | protein_coding | 7/45 | chr2 | 215424620 | ||||||
chr2:215425060
|
C | A | 1 | a0001c0002t0001g0145 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.1036+34G>T | FN1 | ENSG00000115414.21 | transcript | ENST00000354785.11 | protein_coding | 7/45 | chr2 | 215425060 | ||||||
chr2:215425424
|
T | A | 92 | a0001c0001t0001g0002a0001c0001t0001g0062a0001c0001t0001g0149others(89): Show | 93 | HG00099.hp2 HG00280.hp2 HG00609.hp1 others(90): Show |
intron_variant | MODIFIER | c.845-139A>T | FN1 | ENSG00000115414.21 | transcript | ENST00000354785.11 | protein_coding | 6/45 | chr2 | 215425424 | ||||||
chr2:215425479
|
T | C | 2 | a0002c0008t0001g0021a0002c0008t0001g0041 | 2 | HG01175.hp2 HG03017.hp1 |
intron_variant | MODIFIER | c.845-194A>G | FN1 | ENSG00000115414.21 | transcript | ENST00000354785.11 | protein_coding | 6/45 | chr2 | 215425479 | ||||||
chr2:215425535
|
T | C | 2 | a0001c0005t0001g0067a0003c0007t0002g0066 | 2 | HG02717.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.845-250A>G | FN1 | ENSG00000115414.21 | transcript | ENST00000354785.11 | protein_coding | 6/45 | chr2 | 215425535 | ||||||
chr2:215425595
|
C | T | 2 | a0001c0002t0001g0133a0001c0002t0001g0134 | 2 | HG02145.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.845-310G>A | FN1 | ENSG00000115414.21 | transcript | ENST00000354785.11 | protein_coding | 6/45 | chr2 | 215425595 | ||||||
chr2:215425621
|
C | T | 92 | a0001c0001t0001g0002a0001c0001t0001g0062a0001c0001t0001g0149others(89): Show | 93 | HG00099.hp2 HG00280.hp2 HG00609.hp1 others(90): Show |
intron_variant | MODIFIER | c.845-336G>A | FN1 | ENSG00000115414.21 | transcript | ENST00000354785.11 | protein_coding | 6/45 | chr2 | 215425621 | ||||||
chr2:215425699
|
C | T | 5 | a0005c0029t0003g0234a0005c0029t0003g0235a0005c0065t0001g0236others(2): Show | 5 | HG02886.hp1 HG02970.hp2 HG03225.hp1 others(2): Show |
intron_variant | MODIFIER | c.845-414G>A | FN1 | ENSG00000115414.21 | transcript | ENST00000354785.11 | protein_coding | 6/45 | chr2 | 215425699 | ||||||
chr2:215425763
|
GCAAACTC others(20): Show |
G | 2 | a0001c0041t0001g0147a0001c0042t0001g0148 | 2 | HG03540.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.845-505_845-479del others(27): Show |
FN1 | ENSG00000115414.21 | transcript | ENST00000354785.11 | protein_coding | 6/45 | chr2 | 215425763 | ||||||
chr2:215425765
|
A | C | 19 | a0001c0005t0001g0067a0001c0044t0001g0065a0002c0014t0001g0052others(16): Show | 19 | HG01884.hp2 HG01891.hp2 HG01975.hp1 others(16): Show |
intron_variant | MODIFIER | c.845-480T>G | FN1 | ENSG00000115414.21 | transcript | ENST00000354785.11 | protein_coding | 6/45 | chr2 | 215425765 | ||||||
chr2:215425766
|
AACTCCTG others(9): Show |
A | 19 | a0001c0005t0001g0067a0001c0044t0001g0065a0002c0014t0001g0052others(16): Show | 19 | HG01884.hp2 HG01891.hp2 HG01975.hp1 others(16): Show |
intron_variant | MODIFIER | c.845-497_845-482del others(16): Show |
FN1 | ENSG00000115414.21 | transcript | ENST00000354785.11 | protein_coding | 6/45 | chr2 | 215425766 | ||||||
chr2:215425783
|
T | G | 19 | a0001c0005t0001g0067a0001c0044t0001g0065a0002c0014t0001g0052others(16): Show | 19 | HG01884.hp2 HG01891.hp2 HG01975.hp1 others(16): Show |
intron_variant | MODIFIER | c.845-498A>C | FN1 | ENSG00000115414.21 | transcript | ENST00000354785.11 | protein_coding | 6/45 | chr2 | 215425783 | ||||||
chr2:215425784
|
C | G | 19 | a0001c0005t0001g0067a0001c0044t0001g0065a0002c0014t0001g0052others(16): Show | 19 | HG01884.hp2 HG01891.hp2 HG01975.hp1 others(16): Show |
intron_variant | MODIFIER | c.845-499G>C | FN1 | ENSG00000115414.21 | transcript | ENST00000354785.11 | protein_coding | 6/45 | chr2 | 215425784 | ||||||
chr2:215425818
|
C | A | 19 | a0001c0005t0001g0067a0001c0044t0001g0065a0002c0014t0001g0052others(16): Show | 19 | HG01884.hp2 HG01891.hp2 HG01975.hp1 others(16): Show |
intron_variant | MODIFIER | c.845-533G>T | FN1 | ENSG00000115414.21 | transcript | ENST00000354785.11 | protein_coding | 6/45 | chr2 | 215425818 | ||||||
chr2:215425824
|
G | A | 1 | a0001c0011t0001g0220 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.845-539C>T | FN1 | ENSG00000115414.21 | transcript | ENST00000354785.11 | protein_coding | 6/45 | chr2 | 215425824 | ||||||
chr2:215425926
|
C | T | 17 | a0001c0044t0001g0065a0002c0014t0001g0052a0002c0014t0001g0053others(14): Show | 17 | HG01884.hp2 HG01891.hp2 HG01975.hp1 others(14): Show |
intron_variant | MODIFIER | c.845-641G>A | FN1 | ENSG00000115414.21 | transcript | ENST00000354785.11 | protein_coding | 6/45 | chr2 | 215425926 | ||||||
chr2:215425950
|
A | T | 64 | a0001c0002t0001g0111a0001c0002t0001g0112a0001c0002t0001g0113others(61): Show | 64 | HG00140.hp2 HG00323.hp2 HG00642.hp2 others(61): Show |
intron_variant | MODIFIER | c.845-665T>A | FN1 | ENSG00000115414.21 | transcript | ENST00000354785.11 | protein_coding | 6/45 | chr2 | 215425950 | ||||||
chr2:215425956
|
C | T | 7 | a0001c0009t0001g0155a0001c0009t0001g0157a0001c0012t0001g0154others(4): Show | 7 | HG02559.hp2 HG02630.hp1 HG02717.hp1 others(4): Show |
intron_variant | MODIFIER | c.845-671G>A | FN1 | ENSG00000115414.21 | transcript | ENST00000354785.11 | protein_coding | 6/45 | chr2 | 215425956 | ||||||
chr2:215426059
|
T | C | 1 | a0003c0007t0002g0066 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.845-774A>G | FN1 | ENSG00000115414.21 | transcript | ENST00000354785.11 | protein_coding | 6/45 | chr2 | 215426059 | ||||||
chr2:215426122
|
T | C | 1 | a0010c0028t0002g0238 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.845-837A>G | FN1 | ENSG00000115414.21 | transcript | ENST00000354785.11 | protein_coding | 6/45 | chr2 | 215426122 | ||||||
chr2:215426143
|
CT | C | 77 | a0001c0004t0001g0001a0001c0004t0001g0068a0001c0004t0001g0070others(74): Show | 78 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(75): Show |
intron_variant | MODIFIER | c.845-859delA | FN1 | ENSG00000115414.21 | transcript | ENST00000354785.11 | protein_coding | 6/45 | chr2 | 215426143 | ||||||
chr2:215426143
|
CTT | C | 5 | a0001c0001t0001g0171a0001c0001t0001g0173a0001c0058t0002g0153others(2): Show | 5 | HG00323.hp1 HG01106.hp2 HG02109.hp2 others(2): Show |
intron_variant | MODIFIER | c.845-860_845-859del others(2): Show |
FN1 | ENSG00000115414.21 | transcript | ENST00000354785.11 | protein_coding | 6/45 | chr2 | 215426143 | ||||||
chr2:215426143
|
CTTT | C | 86 | a0001c0001t0001g0002a0001c0001t0001g0062a0001c0001t0001g0149others(83): Show | 87 | HG00099.hp2 HG00280.hp2 HG00609.hp1 others(84): Show |
intron_variant | MODIFIER | c.845-861_845-859del others(3): Show |
FN1 | ENSG00000115414.21 | transcript | ENST00000354785.11 | protein_coding | 6/45 | chr2 | 215426143 | ||||||
chr2:215426143
|
CTTTT | C | 25 | a0001c0001t0001g0222a0001c0005t0001g0067a0001c0005t0001g0221others(22): Show | 25 | HG01884.hp2 HG01891.hp2 HG01975.hp1 others(22): Show |
intron_variant | MODIFIER | c.845-862_845-859del others(4): Show |
FN1 | ENSG00000115414.21 | transcript | ENST00000354785.11 | protein_coding | 6/45 | chr2 | 215426143 | ||||||
chr2:215426143
|
CTTTTTTT others(8): Show |
C | 41 | a0001c0002t0001g0111a0001c0002t0001g0112a0001c0002t0001g0113others(38): Show | 41 | HG00140.hp2 HG00323.hp2 HG00642.hp2 others(38): Show |
intron_variant | MODIFIER | c.845-873_845-859del others(15): Show |
FN1 | ENSG00000115414.21 | transcript | ENST00000354785.11 | protein_coding | 6/45 | chr2 | 215426143 | ||||||
chr2:215426153
|
T | C | 5 | a0005c0029t0003g0234a0005c0029t0003g0235a0005c0065t0001g0236others(2): Show | 5 | HG02886.hp1 HG02970.hp2 HG03225.hp1 others(2): Show |
intron_variant | MODIFIER | c.845-868A>G | FN1 | ENSG00000115414.21 | transcript | ENST00000354785.11 | protein_coding | 6/45 | chr2 | 215426153 | ||||||
chr2:215426175
|
G | A | 1 | a0001c0002t0001g0130 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.845-890C>T | FN1 | ENSG00000115414.21 | transcript | ENST00000354785.11 | protein_coding | 6/45 | chr2 | 215426175 | ||||||
chr2:215426297
|
C | T | 3 | a0001c0025t0001g0162a0001c0025t0001g0163a0001c0046t0001g0164 | 3 | HG02055.hp2 HG02258.hp1 HG02723.hp1 |
intron_variant | MODIFIER | c.845-1012G>A | FN1 | ENSG00000115414.21 | transcript | ENST00000354785.11 | protein_coding | 6/45 | chr2 | 215426297 | ||||||
chr2:215426304
|
A | G | 3 | a0001c0025t0001g0162a0001c0025t0001g0163a0001c0046t0001g0164 | 3 | HG02055.hp2 HG02258.hp1 HG02723.hp1 |
intron_variant | MODIFIER | c.845-1019T>C | FN1 | ENSG00000115414.21 | transcript | ENST00000354785.11 | protein_coding | 6/45 | chr2 | 215426304 | ||||||
chr2:215426367
|
C | G | 2 | a0001c0004t0001g0070a0001c0004t0001g0071 | 2 | HG02451.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.845-1082G>C | FN1 | ENSG00000115414.21 | transcript | ENST00000354785.11 | protein_coding | 6/45 | chr2 | 215426367 | ||||||
chr2:215426448
|
G | A | 13 | a0001c0002t0001g0133a0001c0002t0001g0134a0001c0002t0001g0135others(10): Show | 13 | HG01109.hp2 HG01884.hp1 HG02055.hp1 others(10): Show |
intron_variant | MODIFIER | c.845-1163C>T | FN1 | ENSG00000115414.21 | transcript | ENST00000354785.11 | protein_coding | 6/45 | chr2 | 215426448 | ||||||
chr2:215426488
|
G | A | 45 | a0001c0002t0001g0111a0001c0002t0001g0112a0001c0002t0001g0113others(42): Show | 45 | HG00140.hp2 HG00323.hp2 HG00642.hp2 others(42): Show |
intron_variant | MODIFIER | c.845-1203C>T | FN1 | ENSG00000115414.21 | transcript | ENST00000354785.11 | protein_coding | 6/45 | chr2 | 215426488 | ||||||
chr2:215426500
|
C | T | 8 | a0001c0009t0001g0155a0001c0009t0001g0157a0001c0012t0001g0154others(5): Show | 8 | HG02559.hp2 HG02630.hp1 HG02717.hp1 others(5): Show |
intron_variant | MODIFIER | c.845-1215G>A | FN1 | ENSG00000115414.21 | transcript | ENST00000354785.11 | protein_coding | 6/45 | chr2 | 215426500 | ||||||
chr2:215426555
|
C | A | 1 | a0001c0060t0001g0132 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.845-1270G>T | FN1 | ENSG00000115414.21 | transcript | ENST00000354785.11 | protein_coding | 6/45 | chr2 | 215426555 | ||||||
chr2:215426618
|
C | T | 10 | a0001c0044t0001g0065a0004c0019t0001g0004a0004c0019t0001g0007others(7): Show | 10 | HG02258.hp2 HG02647.hp1 HG02886.hp1 others(7): Show |
intron_variant | MODIFIER | c.845-1333G>A | FN1 | ENSG00000115414.21 | transcript | ENST00000354785.11 | protein_coding | 6/45 | chr2 | 215426618 | ||||||
chr2:215426622
|
C | T | 11 | a0001c0006t0001g0110a0001c0009t0001g0155a0001c0009t0001g0157others(8): Show | 11 | HG02109.hp2 HG02559.hp2 HG02630.hp1 others(8): Show |
intron_variant | MODIFIER | c.845-1337G>A | FN1 | ENSG00000115414.21 | transcript | ENST00000354785.11 | protein_coding | 6/45 | chr2 | 215426622 | ||||||
chr2:215426636
|
C | T | 42 | a0001c0004t0001g0070a0001c0004t0001g0071a0001c0004t0001g0080others(39): Show | 42 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(39): Show |
intron_variant | MODIFIER | c.845-1351G>A | FN1 | ENSG00000115414.21 | transcript | ENST00000354785.11 | protein_coding | 6/45 | chr2 | 215426636 | ||||||
chr2:215426705
|
C | T | 1 | a0001c0012t0001g0170 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.845-1420G>A | FN1 | ENSG00000115414.21 | transcript | ENST00000354785.11 | protein_coding | 6/45 | chr2 | 215426705 | ||||||
chr2:215426818
|
C | T | 80 | a0001c0001t0001g0002a0001c0001t0001g0062a0001c0001t0001g0149others(77): Show | 81 | HG00099.hp2 HG00280.hp2 HG00609.hp1 others(78): Show |
intron_variant | MODIFIER | c.844+1362G>A | FN1 | ENSG00000115414.21 | transcript | ENST00000354785.11 | protein_coding | 6/45 | chr2 | 215426818 | ||||||
chr2:215426945
|
G | A | 5 | a0005c0029t0003g0234a0005c0029t0003g0235a0005c0065t0001g0236others(2): Show | 5 | HG02886.hp1 HG02970.hp2 HG03225.hp1 others(2): Show |
intron_variant | MODIFIER | c.844+1235C>T | FN1 | ENSG00000115414.21 | transcript | ENST00000354785.11 | protein_coding | 6/45 | chr2 | 215426945 | ||||||
chr2:215427110
|
C | T | 2 | a0002c0030t0001g0017a0002c0033t0001g0018 | 2 | HG00280.hp1 HG03704.hp1 |
intron_variant | MODIFIER | c.844+1070G>A | FN1 | ENSG00000115414.21 | transcript | ENST00000354785.11 | protein_coding | 6/45 | chr2 | 215427110 | ||||||
chr2:215427117
|
C | T | 42 | a0001c0004t0001g0070a0001c0004t0001g0071a0001c0004t0001g0080others(39): Show | 42 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(39): Show |
intron_variant | MODIFIER | c.844+1063G>A | FN1 | ENSG00000115414.21 | transcript | ENST00000354785.11 | protein_coding | 6/45 | chr2 | 215427117 | ||||||
chr2:215427122
|
G | A | 19 | a0001c0005t0001g0067a0001c0044t0001g0065a0002c0014t0001g0052others(16): Show | 19 | HG01884.hp2 HG01891.hp2 HG01975.hp1 others(16): Show |
intron_variant | MODIFIER | c.844+1058C>T | FN1 | ENSG00000115414.21 | transcript | ENST00000354785.11 | protein_coding | 6/45 | chr2 | 215427122 | ||||||
chr2:215427169
|
G | A | 23 | a0001c0002t0001g0114a0001c0002t0001g0119a0001c0002t0001g0121others(20): Show | 23 | HG00140.hp2 HG00323.hp2 HG00642.hp2 others(20): Show |
intron_variant | MODIFIER | c.844+1011C>T | FN1 | ENSG00000115414.21 | transcript | ENST00000354785.11 | protein_coding | 6/45 | chr2 | 215427169 | ||||||
chr2:215427367
|
G | T | 1 | a0001c0006t0001g0069 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.844+813C>A | FN1 | ENSG00000115414.21 | transcript | ENST00000354785.11 | protein_coding | 6/45 | chr2 | 215427367 | ||||||
chr2:215427590
|
G | A | 5 | a0001c0005t0001g0067a0002c0014t0001g0052a0002c0014t0001g0053others(2): Show | 5 | HG01884.hp2 HG01975.hp1 HG02717.hp2 others(2): Show |
intron_variant | MODIFIER | c.844+590C>T | FN1 | ENSG00000115414.21 | transcript | ENST00000354785.11 | protein_coding | 6/45 | chr2 | 215427590 | ||||||
chr2:215427608
|
G | A | 193 | a0001c0001t0001g0002a0001c0001t0001g0062a0001c0001t0001g0149others(190): Show | 194 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(191): Show |
intron_variant | MODIFIER | c.844+572C>T | FN1 | ENSG00000115414.21 | transcript | ENST00000354785.11 | protein_coding | 6/45 | chr2 | 215427608 | ||||||
chr2:215427706
|
C | T | 1 | a0001c0001t0001g0169 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.844+474G>A | FN1 | ENSG00000115414.21 | transcript | ENST00000354785.11 | protein_coding | 6/45 | chr2 | 215427706 | ||||||
chr2:215427953
|
T | C | 4 | a0001c0001t0001g0226a0009c0016t0001g0223a0009c0016t0001g0224others(1): Show | 4 | HG01257.hp2 HG01258.hp2 HG01952.hp2 others(1): Show |
intron_variant | MODIFIER | c.844+227A>G | FN1 | ENSG00000115414.21 | transcript | ENST00000354785.11 | protein_coding | 6/45 | chr2 | 215427953 | ||||||
chr2:215428054
|
A | G | 7 | a0001c0009t0001g0155a0001c0009t0001g0157a0001c0012t0001g0154others(4): Show | 7 | HG02559.hp2 HG02630.hp1 HG02717.hp1 others(4): Show |
intron_variant | MODIFIER | c.844+126T>C | FN1 | ENSG00000115414.21 | transcript | ENST00000354785.11 | protein_coding | 6/45 | chr2 | 215428054 | ||||||
chr2:215428122
|
C | A | 1 | a0002c0013t0001g0011 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.844+58G>T | FN1 | ENSG00000115414.21 | transcript | ENST00000354785.11 | protein_coding | 6/45 | chr2 | 215428122 | ||||||
chr2:215428747
|
G | A | 1 | a0001c0015t0001g0104 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.686-409C>T | FN1 | ENSG00000115414.21 | transcript | ENST00000354785.11 | protein_coding | 5/45 | chr2 | 215428747 | ||||||
chr2:215428783
|
G | A | 5 | a0001c0044t0001g0065a0004c0019t0001g0004a0004c0019t0001g0007others(2): Show | 5 | HG02258.hp2 HG02647.hp1 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.686-445C>T | FN1 | ENSG00000115414.21 | transcript | ENST00000354785.11 | protein_coding | 5/45 | chr2 | 215428783 | ||||||
chr2:215428888
|
G | A | 5 | a0005c0029t0003g0234a0005c0029t0003g0235a0005c0065t0001g0236others(2): Show | 5 | HG02886.hp1 HG02970.hp2 HG03225.hp1 others(2): Show |
intron_variant | MODIFIER | c.686-550C>T | FN1 | ENSG00000115414.21 | transcript | ENST00000354785.11 | protein_coding | 5/45 | chr2 | 215428888 | ||||||
chr2:215429013
|
AAAAACAA others(3): Show |
A | 1 | a0001c0012t0001g0089 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.686-685_686-676del others(10): Show |
FN1 | ENSG00000115414.21 | transcript | ENST00000354785.11 | protein_coding | 5/45 | chr2 | 215429013 | ||||||
chr2:215429293
|
C | A | 104 | a0001c0002t0001g0111a0001c0002t0001g0112a0001c0002t0001g0113others(101): Show | 105 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(102): Show |
intron_variant | MODIFIER | c.686-955G>T | FN1 | ENSG00000115414.21 | transcript | ENST00000354785.11 | protein_coding | 5/45 | chr2 | 215429293 | ||||||
chr2:215429297
|
A | G | 4 | a0001c0015t0001g0101a0001c0015t0001g0102a0001c0015t0001g0103others(1): Show | 4 | HG02622.hp2 HG02896.hp2 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.686-959T>C | FN1 | ENSG00000115414.21 | transcript | ENST00000354785.11 | protein_coding | 5/45 | chr2 | 215429297 | ||||||
chr2:215429400
|
C | T | 19 | a0001c0005t0001g0067a0001c0044t0001g0065a0002c0014t0001g0052others(16): Show | 19 | HG01884.hp2 HG01891.hp2 HG01975.hp1 others(16): Show |
intron_variant | MODIFIER | c.686-1062G>A | FN1 | ENSG00000115414.21 | transcript | ENST00000354785.11 | protein_coding | 5/45 | chr2 | 215429400 | ||||||
chr2:215429404
|
G | A | 19 | a0001c0005t0001g0067a0001c0044t0001g0065a0002c0014t0001g0052others(16): Show | 19 | HG01884.hp2 HG01891.hp2 HG01975.hp1 others(16): Show |
intron_variant | MODIFIER | c.686-1066C>T | FN1 | ENSG00000115414.21 | transcript | ENST00000354785.11 | protein_coding | 5/45 | chr2 | 215429404 | ||||||
chr2:215429595
|
G | A | 14 | a0001c0044t0001g0065a0002c0014t0001g0056a0002c0023t0001g0049others(11): Show | 14 | HG01891.hp2 HG02257.hp2 HG02258.hp2 others(11): Show |
intron_variant | MODIFIER | c.685+1120C>T | FN1 | ENSG00000115414.21 | transcript | ENST00000354785.11 | protein_coding | 5/45 | chr2 | 215429595 | ||||||
chr2:215429610
|
C | G | 4 | a0001c0015t0001g0101a0001c0015t0001g0102a0001c0015t0001g0103others(1): Show | 4 | HG02622.hp2 HG02896.hp2 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.685+1105G>C | FN1 | ENSG00000115414.21 | transcript | ENST00000354785.11 | protein_coding | 5/45 | chr2 | 215429610 | ||||||
chr2:215429852
|
A | T | 1 | a0002c0003t0001g0016 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.685+863T>A | FN1 | ENSG00000115414.21 | transcript | ENST00000354785.11 | protein_coding | 5/45 | chr2 | 215429852 | ||||||
chr2:215429940
|
G | A | 80 | a0001c0001t0001g0002a0001c0001t0001g0062a0001c0001t0001g0149others(77): Show | 81 | HG00099.hp2 HG00280.hp2 HG00609.hp1 others(78): Show |
intron_variant | MODIFIER | c.685+775C>T | FN1 | ENSG00000115414.21 | transcript | ENST00000354785.11 | protein_coding | 5/45 | chr2 | 215429940 | ||||||
chr2:215429953
|
T | C | 2 | a0001c0006t0001g0110a0001c0058t0002g0153 | 2 | HG02109.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.685+762A>G | FN1 | ENSG00000115414.21 | transcript | ENST00000354785.11 | protein_coding | 5/45 | chr2 | 215429953 | ||||||
chr2:215430026
|
T | C | 7 | a0002c0003t0001g0042a0002c0003t0001g0044a0002c0003t0001g0045others(4): Show | 7 | HG01496.hp1 HG02083.hp2 NA18943.hp2 others(4): Show |
intron_variant | MODIFIER | c.685+689A>G | FN1 | ENSG00000115414.21 | transcript | ENST00000354785.11 | protein_coding | 5/45 | chr2 | 215430026 | ||||||
chr2:215430195
|
C | T | 2 | a0002c0022t0001g0014a0002c0022t0001g0015 | 2 | HG01952.hp1 HG03669.hp2 |
intron_variant | MODIFIER | c.685+520G>A | FN1 | ENSG00000115414.21 | transcript | ENST00000354785.11 | protein_coding | 5/45 | chr2 | 215430195 | ||||||
chr2:215430234
|
C | G | 195 | a0001c0001t0001g0002a0001c0001t0001g0062a0001c0001t0001g0149others(192): Show | 197 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(194): Show |
intron_variant | MODIFIER | c.685+481G>C | FN1 | ENSG00000115414.21 | transcript | ENST00000354785.11 | protein_coding | 5/45 | chr2 | 215430234 | ||||||
chr2:215430290
|
C | T | 5 | a0001c0005t0001g0067a0002c0014t0001g0052a0002c0014t0001g0053others(2): Show | 5 | HG01884.hp2 HG01975.hp1 HG02717.hp2 others(2): Show |
intron_variant | MODIFIER | c.685+425G>A | FN1 | ENSG00000115414.21 | transcript | ENST00000354785.11 | protein_coding | 5/45 | chr2 | 215430290 | ||||||
chr2:215430291
|
A | G | 200 | a0001c0001t0001g0002a0001c0001t0001g0062a0001c0001t0001g0149others(197): Show | 202 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(199): Show |
intron_variant | MODIFIER | c.685+424T>C | FN1 | ENSG00000115414.21 | transcript | ENST00000354785.11 | protein_coding | 5/45 | chr2 | 215430291 | ||||||
chr2:215430468
|
T | G | 41 | a0001c0002t0001g0111a0001c0002t0001g0112a0001c0002t0001g0113others(38): Show | 41 | HG00140.hp2 HG00323.hp2 HG00642.hp2 others(38): Show |
intron_variant | MODIFIER | c.685+247A>C | FN1 | ENSG00000115414.21 | transcript | ENST00000354785.11 | protein_coding | 5/45 | chr2 | 215430468 | ||||||
chr2:215430469
|
G | T | 41 | a0001c0002t0001g0111a0001c0002t0001g0112a0001c0002t0001g0113others(38): Show | 41 | HG00140.hp2 HG00323.hp2 HG00642.hp2 others(38): Show |
intron_variant | MODIFIER | c.685+246C>A | FN1 | ENSG00000115414.21 | transcript | ENST00000354785.11 | protein_coding | 5/45 | chr2 | 215430469 | ||||||
chr2:215430520
|
ATATGTTT others(7): Show |
A | 1 | a0001c0010t0001g0227 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.685+181_685+194del others(14): Show |
FN1 | ENSG00000115414.21 | transcript | ENST00000354785.11 | protein_coding | 5/45 | chr2 | 215430520 | ||||||
chr2:215430558
|
G | A | 41 | a0001c0002t0001g0111a0001c0002t0001g0112a0001c0002t0001g0113others(38): Show | 41 | HG00140.hp2 HG00323.hp2 HG00642.hp2 others(38): Show |
intron_variant | MODIFIER | c.685+157C>T | FN1 | ENSG00000115414.21 | transcript | ENST00000354785.11 | protein_coding | 5/45 | chr2 | 215430558 | ||||||
chr2:215430589
|
T | A | 195 | a0001c0001t0001g0002a0001c0001t0001g0062a0001c0001t0001g0149others(192): Show | 197 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(194): Show |
intron_variant | MODIFIER | c.685+126A>T | FN1 | ENSG00000115414.21 | transcript | ENST00000354785.11 | protein_coding | 5/45 | chr2 | 215430589 | ||||||
chr2:215430614
|
A | G | 41 | a0001c0002t0001g0111a0001c0002t0001g0112a0001c0002t0001g0113others(38): Show | 41 | HG00140.hp2 HG00323.hp2 HG00642.hp2 others(38): Show |
intron_variant | MODIFIER | c.685+101T>C | FN1 | ENSG00000115414.21 | transcript | ENST00000354785.11 | protein_coding | 5/45 | chr2 | 215430614 | ||||||
chr2:215431500
|
AT | A | 18 | a0001c0002t0001g0111a0001c0002t0001g0112a0001c0002t0001g0113others(15): Show | 18 | HG01109.hp2 HG01243.hp1 HG01884.hp1 others(15): Show |
intron_variant | MODIFIER | c.547+332delA | FN1 | ENSG00000115414.21 | transcript | ENST00000354785.11 | protein_coding | 4/45 | chr2 | 215431500 | ||||||
chr2:215431501
|
T | C | 23 | a0001c0002t0001g0114a0001c0002t0001g0119a0001c0002t0001g0121others(20): Show | 23 | HG00140.hp2 HG00323.hp2 HG00642.hp2 others(20): Show |
intron_variant | MODIFIER | c.547+332A>G | FN1 | ENSG00000115414.21 | transcript | ENST00000354785.11 | protein_coding | 4/45 | chr2 | 215431501 | ||||||
chr2:215431502
|
T | C | 18 | a0001c0002t0001g0111a0001c0002t0001g0112a0001c0002t0001g0113others(15): Show | 18 | HG01109.hp2 HG01243.hp1 HG01884.hp1 others(15): Show |
intron_variant | MODIFIER | c.547+331A>G | FN1 | ENSG00000115414.21 | transcript | ENST00000354785.11 | protein_coding | 4/45 | chr2 | 215431502 | ||||||
chr2:215431534
|
G | C | 185 | a0001c0001t0001g0002a0001c0001t0001g0062a0001c0001t0001g0149others(182): Show | 187 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(184): Show |
intron_variant | MODIFIER | c.547+299C>G | FN1 | ENSG00000115414.21 | transcript | ENST00000354785.11 | protein_coding | 4/45 | chr2 | 215431534 | ||||||
chr2:215431791
|
A | T | 1 | a0001c0041t0001g0147 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.547+42T>A | FN1 | ENSG00000115414.21 | transcript | ENST00000354785.11 | protein_coding | 4/45 | chr2 | 215431791 | ||||||
chr2:215431814
|
A | G | 4 | a0004c0019t0001g0004a0004c0019t0001g0007a0004c0020t0002g0005others(1): Show | 4 | HG02647.hp1 HG02922.hp2 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.547+19T>C | FN1 | ENSG00000115414.21 | transcript | ENST00000354785.11 | protein_coding | 4/45 | chr2 | 215431814 | ||||||
chr2:215431981
|
G | A | 2 | a0001c0006t0001g0090a0001c0006t0001g0091 | 2 | HG01256.hp2 HG01258.hp1 |
intron_variant | MODIFIER | c.416-17C>T | FN1 | ENSG00000115414.21 | transcript | ENST00000354785.11 | protein_coding | 3/45 | chr2 | 215431981 | ||||||
chr2:215431997
|
G | A | 1 | a0007c0017t0001g0092 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.416-33C>T | FN1 | ENSG00000115414.21 | transcript | ENST00000354785.11 | protein_coding | 3/45 | chr2 | 215431997 | ||||||
chr2:215432007
|
A | AT | 42 | a0001c0002t0001g0111a0001c0002t0001g0112a0001c0002t0001g0113others(39): Show | 42 | HG00140.hp2 HG00323.hp2 HG00642.hp2 others(39): Show |
intron_variant | MODIFIER | c.416-44dupA | FN1 | ENSG00000115414.21 | transcript | ENST00000354785.11 | protein_coding | 3/45 | chr2 | 215432007 | ||||||
chr2:215432137
|
G | A | 41 | a0001c0002t0001g0111a0001c0002t0001g0112a0001c0002t0001g0113others(38): Show | 41 | HG00140.hp2 HG00323.hp2 HG00642.hp2 others(38): Show |
intron_variant | MODIFIER | c.416-173C>T | FN1 | ENSG00000115414.21 | transcript | ENST00000354785.11 | protein_coding | 3/45 | chr2 | 215432137 | ||||||
chr2:215432471
|
T | C | 9 | a0001c0006t0001g0094a0001c0006t0003g0095a0001c0006t0003g0096others(6): Show | 9 | HG02486.hp1 HG02572.hp1 HG02615.hp1 others(6): Show |
intron_variant | MODIFIER | c.416-507A>G | FN1 | ENSG00000115414.21 | transcript | ENST00000354785.11 | protein_coding | 3/45 | chr2 | 215432471 | ||||||
chr2:215432508
|
T | C | 41 | a0001c0002t0001g0111a0001c0002t0001g0112a0001c0002t0001g0113others(38): Show | 41 | HG00140.hp2 HG00323.hp2 HG00642.hp2 others(38): Show |
intron_variant | MODIFIER | c.416-544A>G | FN1 | ENSG00000115414.21 | transcript | ENST00000354785.11 | protein_coding | 3/45 | chr2 | 215432508 | ||||||
chr2:215432525
|
C | T | 6 | a0001c0009t0001g0166a0001c0009t0002g0167a0001c0025t0001g0162others(3): Show | 6 | HG02055.hp2 HG02258.hp1 HG02647.hp2 others(3): Show |
intron_variant | MODIFIER | c.416-561G>A | FN1 | ENSG00000115414.21 | transcript | ENST00000354785.11 | protein_coding | 3/45 | chr2 | 215432525 | ||||||
chr2:215432565
|
T | A | 4 | a0001c0015t0001g0101a0001c0015t0001g0102a0001c0015t0001g0103others(1): Show | 4 | HG02622.hp2 HG02896.hp2 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.416-601A>T | FN1 | ENSG00000115414.21 | transcript | ENST00000354785.11 | protein_coding | 3/45 | chr2 | 215432565 | ||||||
chr2:215432784
|
T | C | 1 | a0001c0005t0001g0067 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.415+540A>G | FN1 | ENSG00000115414.21 | transcript | ENST00000354785.11 | protein_coding | 3/45 | chr2 | 215432784 | ||||||
chr2:215432933
|
T | C | 85 | a0001c0001t0001g0002a0001c0001t0001g0062a0001c0001t0001g0149others(82): Show | 86 | HG00099.hp2 HG00280.hp2 HG00609.hp1 others(83): Show |
intron_variant | MODIFIER | c.415+391A>G | FN1 | ENSG00000115414.21 | transcript | ENST00000354785.11 | protein_coding | 3/45 | chr2 | 215432933 | ||||||
chr2:215433049
|
G | A | 1 | a0001c0004t0001g0231 | 1 | HG03492.hp2 | intron_variant | MODIFIER | c.415+275C>T | FN1 | ENSG00000115414.21 | transcript | ENST00000354785.11 | protein_coding | 3/45 | chr2 | 215433049 | ||||||
chr2:215433073
|
G | C | 185 | a0001c0001t0001g0002a0001c0001t0001g0062a0001c0001t0001g0149others(182): Show | 187 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(184): Show |
intron_variant | MODIFIER | c.415+251C>G | FN1 | ENSG00000115414.21 | transcript | ENST00000354785.11 | protein_coding | 3/45 | chr2 | 215433073 | ||||||
chr2:215433152
|
G | A | 41 | a0001c0002t0001g0111a0001c0002t0001g0112a0001c0002t0001g0113others(38): Show | 41 | HG00140.hp2 HG00323.hp2 HG00642.hp2 others(38): Show |
intron_variant | MODIFIER | c.415+172C>T | FN1 | ENSG00000115414.21 | transcript | ENST00000354785.11 | protein_coding | 3/45 | chr2 | 215433152 | ||||||
chr2:215433234
|
C | A | 5 | a0005c0029t0003g0234a0005c0029t0003g0235a0005c0065t0001g0236others(2): Show | 5 | HG02886.hp1 HG02970.hp2 HG03225.hp1 others(2): Show |
intron_variant | MODIFIER | c.415+90G>T | FN1 | ENSG00000115414.21 | transcript | ENST00000354785.11 | protein_coding | 3/45 | chr2 | 215433234 | ||||||
chr2:215433479
|
G | A | 1 | a0001c0005t0001g0228 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.278-18C>T | FN1 | ENSG00000115414.21 | transcript | ENST00000354785.11 | protein_coding | 2/45 | chr2 | 215433479 | ||||||
chr2:215433507
|
C | T | 41 | a0001c0002t0001g0111a0001c0002t0001g0112a0001c0002t0001g0113others(38): Show | 41 | HG00140.hp2 HG00323.hp2 HG00642.hp2 others(38): Show |
intron_variant | MODIFIER | c.278-46G>A | FN1 | ENSG00000115414.21 | transcript | ENST00000354785.11 | protein_coding | 2/45 | chr2 | 215433507 | ||||||
chr2:215433520
|
C | T | 1 | a0001c0009t0003g0064 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.278-59G>A | FN1 | ENSG00000115414.21 | transcript | ENST00000354785.11 | protein_coding | 2/45 | chr2 | 215433520 | ||||||
chr2:215433605
|
G | C | 1 | a0002c0003t0001g0057 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.278-144C>G | FN1 | ENSG00000115414.21 | transcript | ENST00000354785.11 | protein_coding | 2/45 | chr2 | 215433605 | ||||||
chr2:215433658
|
C | A | 1 | a0001c0005t0001g0229 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.278-197G>T | FN1 | ENSG00000115414.21 | transcript | ENST00000354785.11 | protein_coding | 2/45 | chr2 | 215433658 | ||||||
chr2:215433690
|
A | C | 8 | a0001c0009t0001g0155a0001c0009t0001g0157a0001c0012t0001g0154others(5): Show | 8 | HG02559.hp2 HG02630.hp1 HG02717.hp1 others(5): Show |
intron_variant | MODIFIER | c.278-229T>G | FN1 | ENSG00000115414.21 | transcript | ENST00000354785.11 | protein_coding | 2/45 | chr2 | 215433690 | ||||||
chr2:215433690
|
A | G | 3 | a0001c0002t0001g0111a0001c0002t0001g0112a0001c0002t0001g0113 | 3 | HG01243.hp1 HG02280.hp1 HG02895.hp1 |
intron_variant | MODIFIER | c.278-229T>C | FN1 | ENSG00000115414.21 | transcript | ENST00000354785.11 | protein_coding | 2/45 | chr2 | 215433690 | ||||||
chr2:215433929
|
C | T | 41 | a0001c0002t0001g0111a0001c0002t0001g0112a0001c0002t0001g0113others(38): Show | 41 | HG00140.hp2 HG00323.hp2 HG00642.hp2 others(38): Show |
intron_variant | MODIFIER | c.278-468G>A | FN1 | ENSG00000115414.21 | transcript | ENST00000354785.11 | protein_coding | 2/45 | chr2 | 215433929 | ||||||
chr2:215434010
|
G | A | 1 | a0001c0010t0001g0230 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.278-549C>T | FN1 | ENSG00000115414.21 | transcript | ENST00000354785.11 | protein_coding | 2/45 | chr2 | 215434010 | ||||||
chr2:215434058
|
T | C | 136 | a0001c0001t0001g0002a0001c0001t0001g0062a0001c0001t0001g0149others(133): Show | 137 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(134): Show |
intron_variant | MODIFIER | c.278-597A>G | FN1 | ENSG00000115414.21 | transcript | ENST00000354785.11 | protein_coding | 2/45 | chr2 | 215434058 | ||||||
chr2:215434143
|
C | T | 2 | a0001c0006t0001g0110a0001c0058t0002g0153 | 2 | HG02109.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.277+553G>A | FN1 | ENSG00000115414.21 | transcript | ENST00000354785.11 | protein_coding | 2/45 | chr2 | 215434143 | ||||||
chr2:215434196
|
CT | C | 5 | a0001c0011t0001g0106a0001c0011t0001g0107a0001c0011t0001g0108others(2): Show | 5 | HG01168.hp1 HG01346.hp1 HG01515.hp2 others(2): Show |
intron_variant | MODIFIER | c.277+499delA | FN1 | ENSG00000115414.21 | transcript | ENST00000354785.11 | protein_coding | 2/45 | chr2 | 215434196 | ||||||
chr2:215434398
|
T | C | 13 | a0001c0002t0001g0133a0001c0002t0001g0134a0001c0002t0001g0135others(10): Show | 13 | HG01109.hp2 HG01884.hp1 HG02055.hp1 others(10): Show |
intron_variant | MODIFIER | c.277+298A>G | FN1 | ENSG00000115414.21 | transcript | ENST00000354785.11 | protein_coding | 2/45 | chr2 | 215434398 | ||||||
chr2:215434408
|
A | AT | 136 | a0001c0001t0001g0002a0001c0001t0001g0062a0001c0001t0001g0149others(133): Show | 137 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(134): Show |
intron_variant | MODIFIER | c.277+287dupA | FN1 | ENSG00000115414.21 | transcript | ENST00000354785.11 | protein_coding | 2/45 | chr2 | 215434408 | ||||||
chr2:215434432
|
A | G | 4 | a0001c0001t0001g0149a0001c0001t0001g0150a0001c0001t0001g0151others(1): Show | 4 | HG02132.hp2 NA18747.hp2 NA18948.hp1 others(1): Show |
intron_variant | MODIFIER | c.277+264T>C | FN1 | ENSG00000115414.21 | transcript | ENST00000354785.11 | protein_coding | 2/45 | chr2 | 215434432 | ||||||
chr2:215434525
|
A | G | 1 | a0002c0003t0001g0013 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.277+171T>C | FN1 | ENSG00000115414.21 | transcript | ENST00000354785.11 | protein_coding | 2/45 | chr2 | 215434525 | ||||||
chr2:215434558
|
A | C | 136 | a0001c0001t0001g0002a0001c0001t0001g0062a0001c0001t0001g0149others(133): Show | 137 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(134): Show |
intron_variant | MODIFIER | c.277+138T>G | FN1 | ENSG00000115414.21 | transcript | ENST00000354785.11 | protein_coding | 2/45 | chr2 | 215434558 | ||||||
chr2:215434636
|
T | G | 1 | a0002c0014t0001g0056 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.277+60A>C | FN1 | ENSG00000115414.21 | transcript | ENST00000354785.11 | protein_coding | 2/45 | chr2 | 215434636 | ||||||
chr2:215434827
|
G | A | 93 | a0001c0001t0001g0002a0001c0001t0001g0062a0001c0001t0001g0149others(90): Show | 94 | HG00099.hp2 HG00280.hp2 HG00609.hp2 others(91): Show |
splice_region_variant&intron_variant | LOW | c.149-3C>T | FN1 | ENSG00000115414.21 | transcript | ENST00000354785.11 | protein_coding | 1/45 | chr2 | 215434827 | ||||||
chr2:215434828
|
C | A | 93 | a0001c0001t0001g0002a0001c0001t0001g0062a0001c0001t0001g0149others(90): Show | 94 | HG00099.hp2 HG00280.hp2 HG00609.hp2 others(91): Show |
splice_region_variant&intron_variant | LOW | c.149-4G>T | FN1 | ENSG00000115414.21 | transcript | ENST00000354785.11 | protein_coding | 1/45 | chr2 | 215434828 | ||||||
chr2:215434848
|
T | TTAC | 135 | a0001c0001t0001g0002a0001c0001t0001g0062a0001c0001t0001g0149others(132): Show | 136 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(133): Show |
intron_variant | MODIFIER | c.149-27_149-25dupGT others(1): Show |
FN1 | ENSG00000115414.21 | transcript | ENST00000354785.11 | protein_coding | 1/45 | chr2 | 215434848 | ||||||
chr2:215434906
|
C | G | 190 | a0001c0001t0001g0002a0001c0001t0001g0062a0001c0001t0001g0149others(187): Show | 192 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(189): Show |
intron_variant | MODIFIER | c.149-82G>C | FN1 | ENSG00000115414.21 | transcript | ENST00000354785.11 | protein_coding | 1/45 | chr2 | 215434906 | ||||||
chr2:215435134
|
G | A | 1 | a0002c0003t0001g0057 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.149-310C>T | FN1 | ENSG00000115414.21 | transcript | ENST00000354785.11 | protein_coding | 1/45 | chr2 | 215435134 | ||||||
chr2:215435179
|
C | T | 1 | a0001c0001t0001g0062 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.149-355G>A | FN1 | ENSG00000115414.21 | transcript | ENST00000354785.11 | protein_coding | 1/45 | chr2 | 215435179 | ||||||
chr2:215435195
|
C | A | 2 | a0001c0002t0001g0232a0001c0002t0001g0233 | 2 | HG03491.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.149-371G>T | FN1 | ENSG00000115414.21 | transcript | ENST00000354785.11 | protein_coding | 1/45 | chr2 | 215435195 | ||||||
chr2:215435462
|
C | T | 187 | a0001c0001t0001g0002a0001c0001t0001g0062a0001c0001t0001g0149others(184): Show | 189 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(186): Show |
intron_variant | MODIFIER | c.148+193G>A | FN1 | ENSG00000115414.21 | transcript | ENST00000354785.11 | protein_coding | 1/45 | chr2 | 215435462 | ||||||
chr2:215435566
|
G | A | 1 | a0002c0037t0001g0058 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.148+89C>T | FN1 | ENSG00000115414.21 | transcript | ENST00000354785.11 | protein_coding | 1/45 | chr2 | 215435566 |