geneid | 54602 |
---|---|
ensemblid | ENSG00000102471.16 |
hgncid | 18537 |
symbol | NDFIP2 |
name | Nedd4 family interacting protein 2 |
refseq_nuc | NM_019080.3 |
refseq_prot | NP_061953.2 |
ensembl_nuc | ENST00000218652.12 |
ensembl_prot | ENSP00000218652.7 |
mane_status | MANE Select |
chr | chr13 |
start | 79481155 |
end | 79556077 |
strand | + |
ver | v1.2 |
region | chr13:79481155-79556077 |
region5000 | chr13:79476155-79561077 |
regionname0 | NDFIP2_chr13_79481155_79556077 |
regionname5000 | NDFIP2_chr13_79476155_79561077 |
ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 1/1 | 336 | 248 | 63 | 41 | 100 | 13 | 29 | 82 | NDFIP2_chr13_79476155_79561077 | NDFIP2 | copy fasta | chr13 | 79476155 | 79561077 |
a0002 | 0/0 | 336 | 16 | 1 | 7 | 0 | 3 | 5 | 0 | NDFIP2_chr13_79476155_79561077 | NDFIP2 | copy fasta | chr13 | 79476155 | 79561077 |
a0003 | 0/0 | 336 | 16 | 15 | 1 | 0 | 0 | 0 | 0 | NDFIP2_chr13_79476155_79561077 | NDFIP2 | copy fasta | chr13 | 79476155 | 79561077 |
a0004 | 0/0 | 336 | 4 | 3 | 1 | 0 | 0 | 0 | 0 | NDFIP2_chr13_79476155_79561077 | NDFIP2 | copy fasta | chr13 | 79476155 | 79561077 |
a0005 | 0/0 | 336 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | NDFIP2_chr13_79476155_79561077 | NDFIP2 | copy fasta | chr13 | 79476155 | 79561077 |
chapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
c0001 | 1/1 | 1011 | 247 | 63 | 41 | 99 | 13 | 29 | NDFIP2_chr13_79476155_79561077 | NDFIP2 | copy fasta | chr13 | 79476155 | 79561077 |
c0002 | 0/0 | 1011 | 16 | 1 | 7 | 0 | 3 | 5 | NDFIP2_chr13_79476155_79561077 | NDFIP2 | copy fasta | chr13 | 79476155 | 79561077 |
c0003 | 0/0 | 1011 | 16 | 15 | 1 | 0 | 0 | 0 | NDFIP2_chr13_79476155_79561077 | NDFIP2 | copy fasta | chr13 | 79476155 | 79561077 |
c0004 | 0/0 | 1011 | 4 | 3 | 1 | 0 | 0 | 0 | NDFIP2_chr13_79476155_79561077 | NDFIP2 | copy fasta | chr13 | 79476155 | 79561077 |
c0005 | 0/0 | 1011 | 2 | 2 | 0 | 0 | 0 | 0 | NDFIP2_chr13_79476155_79561077 | NDFIP2 | copy fasta | chr13 | 79476155 | 79561077 |
c0006 | 0/0 | 1011 | 1 | 0 | 0 | 1 | 0 | 0 | NDFIP2_chr13_79476155_79561077 | NDFIP2 | copy fasta | chr13 | 79476155 | 79561077 |
thapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
t0001 | 1/0 | 3614 | 99 | 22 | 23 | 37 | 6 | 10 | NDFIP2_chr13_79476155_79561077 | NDFIP2 | copy fasta | chr13 | 79476155 | 79561077 |
t0002 | 0/0 | 3614 | 86 | 5 | 12 | 50 | 4 | 15 | NDFIP2_chr13_79476155_79561077 | NDFIP2 | copy fasta | chr13 | 79476155 | 79561077 |
t0003 | 0/0 | 3614 | 37 | 19 | 8 | 1 | 3 | 6 | NDFIP2_chr13_79476155_79561077 | NDFIP2 | copy fasta | chr13 | 79476155 | 79561077 |
t0004 | 0/1 | 3614 | 18 | 13 | 3 | 0 | 1 | 0 | NDFIP2_chr13_79476155_79561077 | NDFIP2 | copy fasta | chr13 | 79476155 | 79561077 |
t0005 | 0/0 | 3614 | 14 | 13 | 1 | 0 | 0 | 0 | NDFIP2_chr13_79476155_79561077 | NDFIP2 | copy fasta | chr13 | 79476155 | 79561077 |
t0006 | 0/0 | 3616 | 9 | 0 | 0 | 6 | 0 | 3 | NDFIP2_chr13_79476155_79561077 | NDFIP2 | copy fasta | chr13 | 79476155 | 79561077 |
t0007 | 0/0 | 3614 | 4 | 3 | 1 | 0 | 0 | 0 | NDFIP2_chr13_79476155_79561077 | NDFIP2 | copy fasta | chr13 | 79476155 | 79561077 |
t0008 | 0/0 | 3614 | 3 | 3 | 0 | 0 | 0 | 0 | NDFIP2_chr13_79476155_79561077 | NDFIP2 | copy fasta | chr13 | 79476155 | 79561077 |
t0009 | 0/0 | 3614 | 2 | 1 | 1 | 0 | 0 | 0 | NDFIP2_chr13_79476155_79561077 | NDFIP2 | copy fasta | chr13 | 79476155 | 79561077 |
t0010 | 0/0 | 3614 | 2 | 2 | 0 | 0 | 0 | 0 | NDFIP2_chr13_79476155_79561077 | NDFIP2 | copy fasta | chr13 | 79476155 | 79561077 |
t0011 | 0/0 | 3614 | 2 | 0 | 0 | 0 | 2 | 0 | NDFIP2_chr13_79476155_79561077 | NDFIP2 | copy fasta | chr13 | 79476155 | 79561077 |
t0012 | 0/0 | 3614 | 1 | 0 | 0 | 1 | 0 | 0 | NDFIP2_chr13_79476155_79561077 | NDFIP2 | copy fasta | chr13 | 79476155 | 79561077 |
t0013 | 0/0 | 3614 | 1 | 0 | 0 | 1 | 0 | 0 | NDFIP2_chr13_79476155_79561077 | NDFIP2 | copy fasta | chr13 | 79476155 | 79561077 |
t0014 | 0/0 | 3614 | 1 | 0 | 1 | 0 | 0 | 0 | NDFIP2_chr13_79476155_79561077 | NDFIP2 | copy fasta | chr13 | 79476155 | 79561077 |
t0015 | 0/0 | 3614 | 1 | 1 | 0 | 0 | 0 | 0 | NDFIP2_chr13_79476155_79561077 | NDFIP2 | copy fasta | chr13 | 79476155 | 79561077 |
t0016 | 0/0 | 3616 | 1 | 0 | 0 | 1 | 0 | 0 | NDFIP2_chr13_79476155_79561077 | NDFIP2 | copy fasta | chr13 | 79476155 | 79561077 |
t0017 | 0/0 | 3614 | 1 | 0 | 0 | 1 | 0 | 0 | NDFIP2_chr13_79476155_79561077 | NDFIP2 | copy fasta | chr13 | 79476155 | 79561077 |
t0018 | 0/0 | 3614 | 1 | 1 | 0 | 0 | 0 | 0 | NDFIP2_chr13_79476155_79561077 | NDFIP2 | copy fasta | chr13 | 79476155 | 79561077 |
t0019 | 0/0 | 3614 | 1 | 1 | 0 | 0 | 0 | 0 | NDFIP2_chr13_79476155_79561077 | NDFIP2 | copy fasta | chr13 | 79476155 | 79561077 |
t0020 | 0/0 | 3614 | 1 | 0 | 0 | 1 | 0 | 0 | NDFIP2_chr13_79476155_79561077 | NDFIP2 | copy fasta | chr13 | 79476155 | 79561077 |
t0021 | 0/0 | 3614 | 1 | 0 | 0 | 1 | 0 | 0 | NDFIP2_chr13_79476155_79561077 | NDFIP2 | copy fasta | chr13 | 79476155 | 79561077 |
ghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
g0001 | 0/0 | 5 | 0 | 1 | 1 | 0 | 3 | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
g0002 | 0/0 | 5 | 0 | 5 | 0 | 0 | 0 | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
g0003 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
g0004 | 0/0 | 4 | 0 | 0 | 1 | 2 | 1 | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
g0005 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
g0006 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
g0007 | 0/0 | 3 | 0 | 0 | 2 | 1 | 0 | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
g0008 | 0/0 | 3 | 0 | 1 | 0 | 1 | 1 | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
g0009 | 0/0 | 3 | 0 | 2 | 0 | 1 | 0 | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
g0010 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
g0011 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
g0012 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
g0013 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
g0014 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
g0015 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
g0016 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
g0017 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
g0018 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
g0019 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
g0020 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
g0021 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
g0022 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
g0023 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
g0024 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
g0025 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
g0026 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
g0027 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
g0039 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
g0044 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
g0045 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
g0047 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
g0048 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
g0049 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
g0050 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
g0059 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
g0066 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
g0070 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
g0079 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
g0088 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
g0089 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
g0092 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
g0097 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
g0098 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
g0099 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
g0100 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
g0102 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
g0111 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
g0112 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
g0113 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
g0115 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
g0118 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
g0123 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
g0124 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
g0125 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
g0127 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
g0140 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
g0144 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
g0145 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
g0146 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
g0147 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
g0148 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
g0149 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
g0150 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
g0151 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
g0152 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
g0153 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
g0154 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
g0162 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
g0164 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
g0169 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
g0170 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
g0172 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
g0173 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
g0179 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
g0185 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
g0189 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
g0190 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
g0191 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
g0192 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
g0197 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
g0198 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
g0199 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
g0201 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
g0202 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
g0206 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
g0207 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
g0208 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
g0213 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
g0215 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
g0218 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
g0225 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
g0230 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
g0239 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
g0243 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
achapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 1/1 | 1011 | 247 | 63 | 41 | 99 | 13 | 29 | NDFIP2_chr13_79476155_79561077 | NDFIP2 | copy fasta | chr13 | 79476155 | 79561077 |
a0001c0006 | 0/0 | 1011 | 1 | 0 | 0 | 1 | 0 | 0 | NDFIP2_chr13_79476155_79561077 | NDFIP2 | copy fasta | chr13 | 79476155 | 79561077 |
a0002c0002 | 0/0 | 1011 | 16 | 1 | 7 | 0 | 3 | 5 | NDFIP2_chr13_79476155_79561077 | NDFIP2 | copy fasta | chr13 | 79476155 | 79561077 |
a0003c0003 | 0/0 | 1011 | 16 | 15 | 1 | 0 | 0 | 0 | NDFIP2_chr13_79476155_79561077 | NDFIP2 | copy fasta | chr13 | 79476155 | 79561077 |
a0004c0004 | 0/0 | 1011 | 4 | 3 | 1 | 0 | 0 | 0 | NDFIP2_chr13_79476155_79561077 | NDFIP2 | copy fasta | chr13 | 79476155 | 79561077 |
a0005c0005 | 0/0 | 1011 | 2 | 2 | 0 | 0 | 0 | 0 | NDFIP2_chr13_79476155_79561077 | NDFIP2 | copy fasta | chr13 | 79476155 | 79561077 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 1/0 | 4624 | 99 | 22 | 23 | 37 | 6 | 10 | NDFIP2_chr13_79476155_79561077 | NDFIP2 | copy fasta | chr13 | 79476155 | 79561077 |
a0001c0001t0002 | 0/0 | 4624 | 84 | 3 | 12 | 50 | 4 | 15 | NDFIP2_chr13_79476155_79561077 | NDFIP2 | copy fasta | chr13 | 79476155 | 79561077 |
a0001c0001t0003 | 0/0 | 4624 | 21 | 18 | 1 | 1 | 0 | 1 | NDFIP2_chr13_79476155_79561077 | NDFIP2 | copy fasta | chr13 | 79476155 | 79561077 |
a0001c0001t0004 | 0/1 | 4624 | 18 | 13 | 3 | 0 | 1 | 0 | NDFIP2_chr13_79476155_79561077 | NDFIP2 | copy fasta | chr13 | 79476155 | 79561077 |
a0001c0001t0006 | 0/0 | 4626 | 8 | 0 | 0 | 5 | 0 | 3 | NDFIP2_chr13_79476155_79561077 | NDFIP2 | copy fasta | chr13 | 79476155 | 79561077 |
a0001c0001t0008 | 0/0 | 4624 | 3 | 3 | 0 | 0 | 0 | 0 | NDFIP2_chr13_79476155_79561077 | NDFIP2 | copy fasta | chr13 | 79476155 | 79561077 |
a0001c0001t0009 | 0/0 | 4624 | 2 | 1 | 1 | 0 | 0 | 0 | NDFIP2_chr13_79476155_79561077 | NDFIP2 | copy fasta | chr13 | 79476155 | 79561077 |
a0001c0001t0011 | 0/0 | 4624 | 2 | 0 | 0 | 0 | 2 | 0 | NDFIP2_chr13_79476155_79561077 | NDFIP2 | copy fasta | chr13 | 79476155 | 79561077 |
a0001c0001t0012 | 0/0 | 4624 | 1 | 0 | 0 | 1 | 0 | 0 | NDFIP2_chr13_79476155_79561077 | NDFIP2 | copy fasta | chr13 | 79476155 | 79561077 |
a0001c0001t0013 | 0/0 | 4624 | 1 | 0 | 0 | 1 | 0 | 0 | NDFIP2_chr13_79476155_79561077 | NDFIP2 | copy fasta | chr13 | 79476155 | 79561077 |
a0001c0001t0014 | 0/0 | 4624 | 1 | 0 | 1 | 0 | 0 | 0 | NDFIP2_chr13_79476155_79561077 | NDFIP2 | copy fasta | chr13 | 79476155 | 79561077 |
a0001c0001t0015 | 0/0 | 4624 | 1 | 1 | 0 | 0 | 0 | 0 | NDFIP2_chr13_79476155_79561077 | NDFIP2 | copy fasta | chr13 | 79476155 | 79561077 |
a0001c0001t0016 | 0/0 | 4626 | 1 | 0 | 0 | 1 | 0 | 0 | NDFIP2_chr13_79476155_79561077 | NDFIP2 | copy fasta | chr13 | 79476155 | 79561077 |
a0001c0001t0017 | 0/0 | 4624 | 1 | 0 | 0 | 1 | 0 | 0 | NDFIP2_chr13_79476155_79561077 | NDFIP2 | copy fasta | chr13 | 79476155 | 79561077 |
a0001c0001t0018 | 0/0 | 4624 | 1 | 1 | 0 | 0 | 0 | 0 | NDFIP2_chr13_79476155_79561077 | NDFIP2 | copy fasta | chr13 | 79476155 | 79561077 |
a0001c0001t0019 | 0/0 | 4624 | 1 | 1 | 0 | 0 | 0 | 0 | NDFIP2_chr13_79476155_79561077 | NDFIP2 | copy fasta | chr13 | 79476155 | 79561077 |
a0001c0001t0020 | 0/0 | 4624 | 1 | 0 | 0 | 1 | 0 | 0 | NDFIP2_chr13_79476155_79561077 | NDFIP2 | copy fasta | chr13 | 79476155 | 79561077 |
a0001c0001t0021 | 0/0 | 4624 | 1 | 0 | 0 | 1 | 0 | 0 | NDFIP2_chr13_79476155_79561077 | NDFIP2 | copy fasta | chr13 | 79476155 | 79561077 |
a0001c0006t0006 | 0/0 | 4626 | 1 | 0 | 0 | 1 | 0 | 0 | NDFIP2_chr13_79476155_79561077 | NDFIP2 | copy fasta | chr13 | 79476155 | 79561077 |
a0002c0002t0003 | 0/0 | 4624 | 16 | 1 | 7 | 0 | 3 | 5 | NDFIP2_chr13_79476155_79561077 | NDFIP2 | copy fasta | chr13 | 79476155 | 79561077 |
a0003c0003t0005 | 0/0 | 4624 | 14 | 13 | 1 | 0 | 0 | 0 | NDFIP2_chr13_79476155_79561077 | NDFIP2 | copy fasta | chr13 | 79476155 | 79561077 |
a0003c0003t0010 | 0/0 | 4624 | 2 | 2 | 0 | 0 | 0 | 0 | NDFIP2_chr13_79476155_79561077 | NDFIP2 | copy fasta | chr13 | 79476155 | 79561077 |
a0004c0004t0007 | 0/0 | 4624 | 4 | 3 | 1 | 0 | 0 | 0 | NDFIP2_chr13_79476155_79561077 | NDFIP2 | copy fasta | chr13 | 79476155 | 79561077 |
a0005c0005t0002 | 0/0 | 4624 | 2 | 2 | 0 | 0 | 0 | 0 | NDFIP2_chr13_79476155_79561077 | NDFIP2 | copy fasta | chr13 | 79476155 | 79561077 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0007 | 0/0 | 2 | 0 | 0 | 1 | 1 | 0 | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
a0001c0001t0001g0008 | 0/0 | 3 | 0 | 1 | 0 | 1 | 1 | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
a0001c0001t0001g0011 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
a0001c0001t0001g0012 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
a0001c0001t0001g0015 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
a0001c0001t0001g0016 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
a0001c0001t0001g0017 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
a0001c0001t0001g0018 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
a0001c0001t0001g0019 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
a0001c0001t0001g0027 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
a0001c0001t0001g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
a0001c0001t0001g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
a0001c0001t0001g0044 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
a0001c0001t0001g0045 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
a0001c0001t0001g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
a0001c0001t0001g0047 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
a0001c0001t0001g0048 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
a0001c0001t0001g0049 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
a0001c0001t0001g0050 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
a0001c0001t0001g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
a0001c0001t0001g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
a0001c0001t0001g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
a0001c0001t0001g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
a0001c0001t0001g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
a0001c0001t0001g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
a0001c0001t0001g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
a0001c0001t0001g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
a0001c0001t0001g0059 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
a0001c0001t0001g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
a0001c0001t0001g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
a0001c0001t0001g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
a0001c0001t0001g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
a0001c0001t0001g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
a0001c0001t0001g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
a0001c0001t0001g0066 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
a0001c0001t0001g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
a0001c0001t0001g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
a0001c0001t0001g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
a0001c0001t0001g0070 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
a0001c0001t0001g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
a0001c0001t0001g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
a0001c0001t0001g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
a0001c0001t0001g0079 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
a0001c0001t0001g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
a0001c0001t0001g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
a0001c0001t0001g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
a0001c0001t0001g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
a0001c0001t0001g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
a0001c0001t0001g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
a0001c0001t0001g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
a0001c0001t0001g0088 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
a0001c0001t0001g0089 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
a0001c0001t0001g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
a0001c0001t0001g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
a0001c0001t0001g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
a0001c0001t0001g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
a0001c0001t0001g0097 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
a0001c0001t0001g0098 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
a0001c0001t0001g0099 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
a0001c0001t0001g0100 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
a0001c0001t0001g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
a0001c0001t0001g0102 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
a0001c0001t0001g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
a0001c0001t0001g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
a0001c0001t0001g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
a0001c0001t0001g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
a0001c0001t0001g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
a0001c0001t0001g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
a0001c0001t0001g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
a0001c0001t0001g0111 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
a0001c0001t0001g0112 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
a0001c0001t0001g0113 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
a0001c0001t0001g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
a0001c0001t0001g0115 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
a0001c0001t0001g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
a0001c0001t0001g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
a0001c0001t0001g0118 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
a0001c0001t0001g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
a0001c0001t0001g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
a0001c0001t0001g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
a0001c0001t0001g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
a0001c0001t0001g0123 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
a0001c0001t0001g0124 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
a0001c0001t0001g0125 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
a0001c0001t0001g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
a0001c0001t0001g0162 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
a0001c0001t0001g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
a0001c0001t0001g0206 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
a0001c0001t0001g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
a0001c0001t0002g0001 | 0/0 | 5 | 0 | 1 | 1 | 0 | 3 | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
a0001c0001t0002g0002 | 0/0 | 4 | 0 | 4 | 0 | 0 | 0 | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
a0001c0001t0002g0004 | 0/0 | 4 | 0 | 0 | 1 | 2 | 1 | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
a0001c0001t0002g0005 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
a0001c0001t0002g0023 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
a0001c0001t0002g0024 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
a0001c0001t0002g0025 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
a0001c0001t0002g0026 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
a0001c0001t0002g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
a0001c0001t0002g0164 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
a0001c0001t0002g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
a0001c0001t0002g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
a0001c0001t0002g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
a0001c0001t0002g0169 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
a0001c0001t0002g0170 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
a0001c0001t0002g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
a0001c0001t0002g0172 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
a0001c0001t0002g0173 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
a0001c0001t0002g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
a0001c0001t0002g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
a0001c0001t0002g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
a0001c0001t0002g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
a0001c0001t0002g0179 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
a0001c0001t0002g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
a0001c0001t0002g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
a0001c0001t0002g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
a0001c0001t0002g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
a0001c0001t0002g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
a0001c0001t0002g0185 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
a0001c0001t0002g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
a0001c0001t0002g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
a0001c0001t0002g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
a0001c0001t0002g0189 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
a0001c0001t0002g0190 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
a0001c0001t0002g0191 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
a0001c0001t0002g0192 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
a0001c0001t0002g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
a0001c0001t0002g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
a0001c0001t0002g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
a0001c0001t0002g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
a0001c0001t0002g0197 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
a0001c0001t0002g0198 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
a0001c0001t0002g0199 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
a0001c0001t0002g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
a0001c0001t0002g0201 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
a0001c0001t0002g0202 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
a0001c0001t0002g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
a0001c0001t0002g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
a0001c0001t0002g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
a0001c0001t0002g0207 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
a0001c0001t0002g0208 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
a0001c0001t0002g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
a0001c0001t0002g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
a0001c0001t0002g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
a0001c0001t0002g0213 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
a0001c0001t0002g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
a0001c0001t0002g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
a0001c0001t0002g0230 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
a0001c0001t0002g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
a0001c0001t0002g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
a0001c0001t0002g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
a0001c0001t0002g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
a0001c0001t0002g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
a0001c0001t0002g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
a0001c0001t0002g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
a0001c0001t0002g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
a0001c0001t0002g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
a0001c0001t0003g0006 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
a0001c0001t0003g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
a0001c0001t0003g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
a0001c0001t0003g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
a0001c0001t0003g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
a0001c0001t0003g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
a0001c0001t0003g0218 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
a0001c0001t0003g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
a0001c0001t0003g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
a0001c0001t0003g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
a0001c0001t0003g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
a0001c0001t0003g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
a0001c0001t0003g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
a0001c0001t0003g0225 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
a0001c0001t0003g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
a0001c0001t0003g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
a0001c0001t0003g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
a0001c0001t0003g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
a0001c0001t0004g0003 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
a0001c0001t0004g0009 | 0/0 | 3 | 0 | 2 | 0 | 1 | 0 | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
a0001c0001t0004g0020 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
a0001c0001t0004g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
a0001c0001t0004g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
a0001c0001t0004g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
a0001c0001t0004g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
a0001c0001t0004g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
a0001c0001t0004g0140 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
a0001c0001t0004g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
a0001c0001t0004g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
a0001c0001t0004g0215 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
a0001c0001t0006g0013 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
a0001c0001t0006g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
a0001c0001t0006g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
a0001c0001t0006g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
a0001c0001t0006g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
a0001c0001t0006g0092 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
a0001c0001t0006g0243 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
a0001c0001t0008g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
a0001c0001t0008g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
a0001c0001t0008g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
a0001c0001t0009g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
a0001c0001t0009g0239 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
a0001c0001t0011g0014 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
a0001c0001t0012g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
a0001c0001t0013g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
a0001c0001t0014g0002 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
a0001c0001t0015g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
a0001c0001t0016g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
a0001c0001t0017g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
a0001c0001t0018g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
a0001c0001t0019g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
a0001c0001t0020g0007 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
a0001c0001t0021g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
a0001c0006t0006g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
a0002c0002t0003g0021 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
a0002c0002t0003g0022 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
a0002c0002t0003g0144 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
a0002c0002t0003g0145 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
a0002c0002t0003g0146 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
a0002c0002t0003g0147 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
a0002c0002t0003g0148 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
a0002c0002t0003g0149 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
a0002c0002t0003g0150 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
a0002c0002t0003g0151 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
a0002c0002t0003g0152 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
a0002c0002t0003g0153 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
a0002c0002t0003g0154 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
a0002c0002t0003g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
a0003c0003t0005g0010 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
a0003c0003t0005g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
a0003c0003t0005g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
a0003c0003t0005g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
a0003c0003t0005g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
a0003c0003t0005g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
a0003c0003t0005g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
a0003c0003t0005g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
a0003c0003t0005g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
a0003c0003t0005g0039 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
a0003c0003t0005g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
a0003c0003t0005g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
a0003c0003t0005g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
a0003c0003t0010g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
a0003c0003t0010g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
a0004c0004t0007g0127 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
a0004c0004t0007g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
a0004c0004t0007g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
a0004c0004t0007g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
a0005c0005t0002g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
a0005c0005t0002g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0001 | c0001 | t0002 | g0004 | EUR | GBR | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
HG00099 | hp2 | a0001 | c0001 | t0001 | g0088 | EUR | GBR | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
HG00140 | hp1 | a0002 | c0002 | t0003 | g0151 | EUR | GBR | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
HG00140 | hp2 | a0001 | c0001 | t0001 | g0059 | EUR | GBR | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
HG00280 | hp1 | a0002 | c0002 | t0003 | g0150 | EUR | FIN | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
HG00280 | hp2 | a0001 | c0001 | t0001 | g0044 | EUR | FIN | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
HG00323 | hp1 | a0001 | c0001 | t0002 | g0004 | EUR | FIN | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
HG00323 | hp2 | a0001 | c0001 | t0001 | g0007 | EUR | FIN | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
HG00408 | hp1 | a0001 | c0001 | t0001 | g0060 | EAS | CHS | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
HG00408 | hp2 | a0001 | c0001 | t0002 | g0005 | EAS | CHS | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
HG00544 | hp1 | a0001 | c0001 | t0001 | g0096 | EAS | CHS | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
HG00544 | hp2 | a0001 | c0001 | t0002 | g0183 | EAS | CHS | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
HG00733 | hp1 | a0002 | c0002 | t0003 | g0148 | AMR | PUR | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
HG00733 | hp2 | a0001 | c0001 | t0001 | g0015 | AMR | PUR | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
HG00735 | hp1 | a0001 | c0001 | t0001 | g0125 | AMR | PUR | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
HG00735 | hp2 | a0001 | c0001 | t0003 | g0218 | AMR | PUR | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
HG00738 | hp1 | a0001 | c0001 | t0001 | g0015 | AMR | PUR | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
HG00738 | hp2 | a0001 | c0001 | t0001 | g0113 | AMR | PUR | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
HG00741 | hp1 | a0001 | c0001 | t0002 | g0230 | AMR | PUR | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
HG00741 | hp2 | a0001 | c0001 | t0014 | g0002 | AMR | PUR | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
HG01069 | hp1 | a0001 | c0001 | t0004 | g0009 | AMR | PUR | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
HG01069 | hp2 | a0002 | c0002 | t0003 | g0022 | AMR | PUR | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
HG01071 | hp1 | a0001 | c0001 | t0004 | g0009 | AMR | PUR | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
HG01071 | hp2 | a0001 | c0001 | t0002 | g0002 | AMR | PUR | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
HG01074 | hp1 | a0001 | c0001 | t0002 | g0197 | AMR | PUR | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
HG01074 | hp2 | a0001 | c0001 | t0001 | g0008 | AMR | PUR | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
HG01109 | hp1 | a0001 | c0001 | t0001 | g0079 | AMR | PUR | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
HG01109 | hp2 | a0001 | c0001 | t0002 | g0002 | AMR | PUR | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
HG01167 | hp1 | a0001 | c0001 | t0002 | g0190 | AMR | PUR | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
HG01167 | hp2 | a0002 | c0002 | t0003 | g0146 | AMR | PUR | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
HG01168 | hp1 | a0002 | c0002 | t0003 | g0153 | AMR | PUR | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
HG01168 | hp2 | a0001 | c0001 | t0002 | g0001 | AMR | PUR | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
HG01175 | hp1 | a0001 | c0001 | t0001 | g0066 | AMR | PUR | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
HG01175 | hp2 | a0002 | c0002 | t0003 | g0147 | AMR | PUR | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
HG01192 | hp1 | a0001 | c0001 | t0001 | g0123 | AMR | PUR | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
HG01192 | hp2 | a0002 | c0002 | t0003 | g0022 | AMR | PUR | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
HG01243 | hp1 | a0001 | c0001 | t0009 | g0239 | AMR | PUR | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
HG01243 | hp2 | a0001 | c0001 | t0004 | g0140 | AMR | PUR | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
HG01256 | hp1 | a0001 | c0001 | t0001 | g0089 | AMR | CLM | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
HG01256 | hp2 | a0001 | c0001 | t0002 | g0002 | AMR | CLM | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
HG01258 | hp1 | a0001 | c0001 | t0001 | g0102 | AMR | CLM | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
HG01258 | hp2 | a0001 | c0001 | t0002 | g0002 | AMR | CLM | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
HG01261 | hp1 | a0001 | c0001 | t0002 | g0213 | AMR | CLM | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
HG01261 | hp2 | a0001 | c0001 | t0001 | g0124 | AMR | CLM | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
HG01346 | hp1 | a0001 | c0001 | t0001 | g0016 | AMR | CLM | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
HG01346 | hp2 | a0001 | c0001 | t0002 | g0198 | AMR | CLM | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
HG01361 | hp1 | a0001 | c0001 | t0002 | g0202 | AMR | CLM | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
HG01361 | hp2 | a0002 | c0002 | t0003 | g0145 | AMR | CLM | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
HG01496 | hp1 | a0001 | c0001 | t0001 | g0111 | AMR | CLM | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
HG01496 | hp2 | a0001 | c0001 | t0001 | g0115 | AMR | CLM | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
HG01515 | hp1 | a0001 | c0001 | t0004 | g0009 | EUR | IBS | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
HG01515 | hp2 | a0001 | c0001 | t0011 | g0014 | EUR | IBS | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
HG01517 | hp1 | a0001 | c0001 | t0011 | g0014 | EUR | IBS | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
HG01517 | hp2 | a0001 | c0001 | t0001 | g0162 | EUR | IBS | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
HG01884 | hp1 | a0001 | c0001 | t0001 | g0055 | AFR | ACB | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
HG01884 | hp2 | a0001 | c0001 | t0003 | g0226 | AFR | ACB | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
HG01891 | hp1 | a0001 | c0001 | t0001 | g0117 | AFR | ACB | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
HG01891 | hp2 | a0001 | c0001 | t0004 | g0133 | AFR | ACB | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
HG01934 | hp1 | a0001 | c0001 | t0001 | g0099 | AMR | PEL | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
HG01934 | hp2 | a0001 | c0001 | t0001 | g0116 | AMR | PEL | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
HG01943 | hp1 | a0001 | c0001 | t0001 | g0101 | AMR | PEL | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
HG01943 | hp2 | a0001 | c0001 | t0001 | g0070 | AMR | PEL | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
HG01952 | hp1 | a0004 | c0004 | t0007 | g0127 | AMR | PEL | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
HG01952 | hp2 | a0001 | c0001 | t0001 | g0098 | AMR | PEL | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
HG01978 | hp1 | a0001 | c0001 | t0001 | g0027 | AMR | PEL | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
HG01978 | hp2 | a0001 | c0001 | t0001 | g0100 | AMR | PEL | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
HG01981 | hp1 | a0001 | c0001 | t0001 | g0112 | AMR | PEL | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
HG01981 | hp2 | a0003 | c0003 | t0005 | g0039 | AMR | PEL | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
HG02040 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | KHV | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
HG02040 | hp2 | a0001 | c0006 | t0006 | g0084 | EAS | KHV | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
HG02055 | hp1 | a0001 | c0001 | t0003 | g0220 | AFR | ACB | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
HG02055 | hp2 | a0001 | c0001 | t0009 | g0209 | AFR | ACB | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
HG02071 | hp1 | a0001 | c0001 | t0002 | g0231 | EAS | KHV | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
HG02071 | hp2 | a0001 | c0001 | t0001 | g0067 | EAS | KHV | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
HG02074 | hp1 | a0001 | c0001 | t0006 | g0013 | EAS | KHV | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
HG02074 | hp2 | a0001 | c0001 | t0002 | g0182 | EAS | KHV | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
HG02080 | hp1 | a0001 | c0001 | t0001 | g0121 | EAS | KHV | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
HG02080 | hp2 | a0001 | c0001 | t0002 | g0025 | EAS | KHV | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
HG02129 | hp1 | a0001 | c0001 | t0002 | g0005 | EAS | KHV | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
HG02129 | hp2 | a0001 | c0001 | t0006 | g0074 | EAS | KHV | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
HG02145 | hp1 | a0004 | c0004 | t0007 | g0141 | AFR | ACB | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
HG02145 | hp2 | a0001 | c0001 | t0003 | g0216 | AFR | ACB | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
HG02165 | hp1 | a0001 | c0001 | t0002 | g0178 | EAS | CDX | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
HG02165 | hp2 | a0001 | c0001 | t0001 | g0062 | EAS | CDX | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
HG02257 | hp1 | a0001 | c0001 | t0003 | g0241 | AFR | ACB | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
HG02257 | hp2 | a0001 | c0001 | t0003 | g0227 | AFR | ACB | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
HG02258 | hp1 | a0001 | c0001 | t0001 | g0091 | AFR | ACB | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
HG02258 | hp2 | a0001 | c0001 | t0002 | g0156 | AFR | ACB | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
HG02280 | hp1 | a0001 | c0001 | t0002 | g0204 | AFR | ACB | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
HG02280 | hp2 | a0001 | c0001 | t0001 | g0086 | AFR | ACB | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
HG02300 | hp1 | a0001 | c0001 | t0001 | g0118 | AMR | PEL | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
HG02300 | hp2 | a0001 | c0001 | t0002 | g0208 | AMR | PEL | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
HG02451 | hp1 | a0003 | c0003 | t0005 | g0038 | AFR | ACB | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
HG02451 | hp2 | a0001 | c0001 | t0003 | g0217 | AFR | ACB | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
HG02523 | hp1 | a0001 | c0001 | t0002 | g0005 | EAS | KHV | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
HG02523 | hp2 | a0001 | c0001 | t0006 | g0076 | EAS | KHV | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
HG02572 | hp1 | a0001 | c0001 | t0004 | g0134 | AFR | GWD | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
HG02572 | hp2 | a0001 | c0001 | t0003 | g0228 | AFR | GWD | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
HG02615 | hp1 | a0001 | c0001 | t0004 | g0136 | AFR | GWD | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
HG02615 | hp2 | a0004 | c0004 | t0007 | g0129 | AFR | GWD | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
HG02622 | hp1 | a0001 | c0001 | t0004 | g0003 | AFR | GWD | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
HG02622 | hp2 | a0003 | c0003 | t0005 | g0029 | AFR | GWD | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
HG02630 | hp1 | a0001 | c0001 | t0001 | g0057 | AFR | GWD | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
HG02630 | hp2 | a0001 | c0001 | t0001 | g0012 | AFR | GWD | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
HG02698 | hp1 | a0002 | c0002 | t0003 | g0144 | SAS | PJL | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
HG02698 | hp2 | a0001 | c0001 | t0001 | g0049 | SAS | PJL | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
HG02717 | hp1 | a0001 | c0001 | t0003 | g0158 | AFR | GWD | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
HG02717 | hp2 | a0001 | c0001 | t0015 | g0078 | AFR | GWD | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
HG02723 | hp1 | a0001 | c0001 | t0008 | g0131 | AFR | GWD | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
HG02723 | hp2 | a0003 | c0003 | t0005 | g0042 | AFR | GWD | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
HG02735 | hp1 | a0001 | c0001 | t0001 | g0016 | SAS | PJL | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
HG02735 | hp2 | a0001 | c0001 | t0002 | g0001 | SAS | PJL | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
HG02809 | hp1 | a0001 | c0001 | t0018 | g0137 | AFR | GWD | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
HG02809 | hp2 | a0001 | c0001 | t0001 | g0083 | AFR | GWD | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
HG02886 | hp1 | a0001 | c0001 | t0008 | g0132 | AFR | GWD | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
HG02886 | hp2 | a0001 | c0001 | t0002 | g0229 | AFR | GWD | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
HG02895 | hp1 | a0002 | c0002 | t0003 | g0160 | AFR | GWD | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
HG02895 | hp2 | a0003 | c0003 | t0005 | g0030 | AFR | GWD | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
HG02897 | hp1 | a0001 | c0001 | t0001 | g0080 | AFR | GWD | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
HG02897 | hp2 | a0003 | c0003 | t0005 | g0031 | AFR | GWD | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
HG02922 | hp1 | a0001 | c0001 | t0001 | g0051 | AFR | ESN | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
HG02922 | hp2 | a0001 | c0001 | t0003 | g0006 | AFR | ESN | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
HG02965 | hp1 | a0001 | c0001 | t0003 | g0161 | AFR | ESN | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
HG02965 | hp2 | a0003 | c0003 | t0010 | g0034 | AFR | ESN | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
HG02976 | hp1 | a0001 | c0001 | t0003 | g0006 | AFR | ESN | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
HG02976 | hp2 | a0001 | c0001 | t0003 | g0222 | AFR | ESN | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
HG03017 | hp1 | a0001 | c0001 | t0003 | g0225 | SAS | PJL | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
HG03017 | hp2 | a0001 | c0001 | t0001 | g0011 | SAS | PJL | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
HG03041 | hp1 | a0001 | c0001 | t0001 | g0082 | AFR | GWD | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
HG03041 | hp2 | a0001 | c0001 | t0004 | g0142 | AFR | GWD | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
HG03098 | hp1 | a0001 | c0001 | t0004 | g0003 | AFR | MSL | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
HG03098 | hp2 | a0003 | c0003 | t0005 | g0037 | AFR | MSL | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
HG03130 | hp1 | a0001 | c0001 | t0001 | g0063 | AFR | ESN | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
HG03130 | hp2 | a0003 | c0003 | t0005 | g0041 | AFR | ESN | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
HG03195 | hp1 | a0001 | c0001 | t0003 | g0221 | AFR | ESN | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
HG03195 | hp2 | a0001 | c0001 | t0004 | g0003 | AFR | ESN | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
HG03225 | hp1 | a0001 | c0001 | t0001 | g0053 | AFR | MSL | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
HG03225 | hp2 | a0001 | c0001 | t0003 | g0159 | AFR | MSL | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
HG03239 | hp1 | a0001 | c0001 | t0002 | g0199 | SAS | PJL | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
HG03239 | hp2 | a0001 | c0001 | t0001 | g0011 | SAS | PJL | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
HG03453 | hp1 | a0003 | c0003 | t0005 | g0033 | AFR | MSL | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
HG03453 | hp2 | a0001 | c0001 | t0001 | g0052 | AFR | MSL | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
HG03486 | hp1 | a0001 | c0001 | t0001 | g0119 | AFR | MSL | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
HG03486 | hp2 | a0001 | c0001 | t0001 | g0046 | AFR | MSL | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
HG03490 | hp1 | a0001 | c0001 | t0002 | g0001 | SAS | PJL | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
HG03490 | hp2 | a0002 | c0002 | t0003 | g0021 | SAS | PJL | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
HG03492 | hp1 | a0001 | c0001 | t0002 | g0173 | SAS | PJL | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
HG03492 | hp2 | a0002 | c0002 | t0003 | g0021 | SAS | PJL | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
HG03516 | hp1 | a0001 | c0001 | t0003 | g0006 | AFR | ESN | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
HG03516 | hp2 | a0001 | c0001 | t0003 | g0219 | AFR | ESN | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
HG03540 | hp1 | a0001 | c0001 | t0004 | g0020 | AFR | GWD | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
HG03540 | hp2 | a0003 | c0003 | t0005 | g0036 | AFR | GWD | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
HG03579 | hp1 | a0001 | c0001 | t0004 | g0143 | AFR | MSL | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
HG03579 | hp2 | a0001 | c0001 | t0008 | g0130 | AFR | MSL | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
HG03654 | hp1 | a0001 | c0001 | t0001 | g0050 | SAS | PJL | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
HG03654 | hp2 | a0001 | c0001 | t0002 | g0164 | SAS | PJL | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
HG03669 | hp1 | a0001 | c0001 | t0002 | g0201 | SAS | PJL | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
HG03669 | hp2 | a0001 | c0001 | t0001 | g0097 | SAS | PJL | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
HG03688 | hp1 | a0001 | c0001 | t0002 | g0169 | SAS | STU | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
HG03688 | hp2 | a0002 | c0002 | t0003 | g0152 | SAS | STU | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
HG03710 | hp1 | a0001 | c0001 | t0002 | g0191 | SAS | PJL | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
HG03710 | hp2 | a0001 | c0001 | t0006 | g0092 | SAS | PJL | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
HG03831 | hp1 | a0001 | c0001 | t0002 | g0170 | SAS | BEB | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
HG03831 | hp2 | a0001 | c0001 | t0001 | g0045 | SAS | BEB | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
HG03834 | hp1 | a0001 | c0001 | t0001 | g0048 | SAS | BEB | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
HG03834 | hp2 | a0001 | c0001 | t0002 | g0185 | SAS | BEB | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
HG03942 | hp1 | a0001 | c0001 | t0006 | g0243 | SAS | BEB | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
HG03942 | hp2 | a0002 | c0002 | t0003 | g0154 | SAS | BEB | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
HG04184 | hp1 | a0001 | c0001 | t0006 | g0013 | SAS | BEB | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
HG04184 | hp2 | a0001 | c0001 | t0002 | g0004 | SAS | BEB | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
HG04199 | hp1 | a0001 | c0001 | t0001 | g0008 | SAS | STU | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
HG04199 | hp2 | a0001 | c0001 | t0002 | g0179 | SAS | STU | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
HG04204 | hp1 | a0001 | c0001 | t0002 | g0189 | SAS | STU | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
HG04204 | hp2 | a0001 | c0001 | t0002 | g0172 | SAS | STU | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
HG04228 | hp1 | a0001 | c0001 | t0002 | g0001 | SAS | STU | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
HG04228 | hp2 | a0001 | c0001 | t0001 | g0047 | SAS | STU | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
NA18522 | hp1 | a0001 | c0001 | t0001 | g0095 | AFR | YRI | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
NA18522 | hp2 | a0003 | c0003 | t0010 | g0035 | AFR | YRI | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
NA18906 | hp1 | a0001 | c0001 | t0004 | g0020 | AFR | YRI | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
NA18906 | hp2 | a0005 | c0005 | t0002 | g0155 | AFR | YRI | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
NA18939 | hp1 | a0001 | c0001 | t0002 | g0005 | EAS | JPT | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
NA18939 | hp2 | a0001 | c0001 | t0003 | g0224 | EAS | JPT | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
NA18940 | hp1 | a0001 | c0001 | t0001 | g0056 | EAS | JPT | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
NA18940 | hp2 | a0001 | c0001 | t0002 | g0181 | EAS | JPT | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
NA18941 | hp1 | a0001 | c0001 | t0002 | g0194 | EAS | JPT | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
NA18941 | hp2 | a0001 | c0001 | t0002 | g0171 | EAS | JPT | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
NA18942 | hp1 | a0001 | c0001 | t0002 | g0004 | EAS | JPT | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
NA18942 | hp2 | a0001 | c0001 | t0001 | g0068 | EAS | JPT | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
NA18943 | hp1 | a0001 | c0001 | t0001 | g0087 | EAS | JPT | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
NA18943 | hp2 | a0001 | c0001 | t0002 | g0175 | EAS | JPT | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
NA18944 | hp1 | a0001 | c0001 | t0002 | g0024 | EAS | JPT | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
NA18944 | hp2 | a0001 | c0001 | t0001 | g0018 | EAS | JPT | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
NA18945 | hp1 | a0001 | c0001 | t0002 | g0193 | EAS | JPT | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
NA18945 | hp2 | a0001 | c0001 | t0021 | g0073 | EAS | JPT | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
NA18954 | hp1 | a0001 | c0001 | t0002 | g0234 | EAS | JPT | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
NA18954 | hp2 | a0001 | c0001 | t0001 | g0105 | EAS | JPT | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
NA18959 | hp1 | a0001 | c0001 | t0001 | g0104 | EAS | JPT | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
NA18959 | hp2 | a0001 | c0001 | t0002 | g0024 | EAS | JPT | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
NA18962 | hp1 | a0001 | c0001 | t0002 | g0166 | EAS | JPT | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
NA18962 | hp2 | a0001 | c0001 | t0002 | g0026 | EAS | JPT | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
NA18969 | hp1 | a0001 | c0001 | t0001 | g0017 | EAS | JPT | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
NA18969 | hp2 | a0001 | c0001 | t0002 | g0212 | EAS | JPT | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
NA18973 | hp1 | a0001 | c0001 | t0001 | g0069 | EAS | JPT | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
NA18973 | hp2 | a0001 | c0001 | t0002 | g0205 | EAS | JPT | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
NA18975 | hp1 | a0001 | c0001 | t0001 | g0058 | EAS | JPT | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
NA18975 | hp2 | a0001 | c0001 | t0002 | g0026 | EAS | JPT | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
NA18977 | hp1 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
NA18977 | hp2 | a0001 | c0001 | t0002 | g0240 | EAS | JPT | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
NA18979 | hp1 | a0001 | c0001 | t0001 | g0019 | EAS | JPT | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
NA18979 | hp2 | a0001 | c0001 | t0017 | g0094 | EAS | JPT | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
NA18982 | hp1 | a0001 | c0001 | t0001 | g0043 | EAS | JPT | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
NA18982 | hp2 | a0001 | c0001 | t0002 | g0023 | EAS | JPT | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
NA18986 | hp1 | a0001 | c0001 | t0001 | g0106 | EAS | JPT | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
NA18986 | hp2 | a0001 | c0001 | t0013 | g0167 | EAS | JPT | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
NA18987 | hp1 | a0001 | c0001 | t0001 | g0126 | EAS | JPT | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
NA18987 | hp2 | a0001 | c0001 | t0002 | g0236 | EAS | JPT | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
NA18988 | hp1 | a0001 | c0001 | t0001 | g0093 | EAS | JPT | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
NA18988 | hp2 | a0001 | c0001 | t0002 | g0195 | EAS | JPT | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
NA18990 | hp1 | a0001 | c0001 | t0012 | g0177 | EAS | JPT | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
NA18990 | hp2 | a0001 | c0001 | t0002 | g0214 | EAS | JPT | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
NA18991 | hp1 | a0001 | c0001 | t0002 | g0238 | EAS | JPT | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
NA18991 | hp2 | a0001 | c0001 | t0001 | g0064 | EAS | JPT | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
NA18995 | hp1 | a0001 | c0001 | t0002 | g0188 | EAS | JPT | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
NA18995 | hp2 | a0001 | c0001 | t0001 | g0242 | EAS | JPT | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
NA19002 | hp1 | a0001 | c0001 | t0016 | g0110 | EAS | JPT | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
NA19002 | hp2 | a0001 | c0001 | t0001 | g0163 | EAS | JPT | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
NA19006 | hp1 | a0001 | c0001 | t0001 | g0085 | EAS | JPT | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
NA19006 | hp2 | a0001 | c0001 | t0002 | g0210 | EAS | JPT | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
NA19043 | hp1 | a0005 | c0005 | t0002 | g0157 | AFR | LWK | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
NA19043 | hp2 | a0001 | c0001 | t0001 | g0072 | AFR | LWK | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
NA19054 | hp1 | a0001 | c0001 | t0002 | g0176 | EAS | JPT | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
NA19054 | hp2 | a0001 | c0001 | t0001 | g0103 | EAS | JPT | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
NA19055 | hp1 | a0001 | c0001 | t0001 | g0018 | EAS | JPT | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
NA19055 | hp2 | a0001 | c0001 | t0002 | g0196 | EAS | JPT | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
NA19057 | hp1 | a0001 | c0001 | t0001 | g0017 | EAS | JPT | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
NA19057 | hp2 | a0001 | c0001 | t0002 | g0203 | EAS | JPT | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
NA19060 | hp1 | a0001 | c0001 | t0002 | g0023 | EAS | JPT | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
NA19060 | hp2 | a0001 | c0001 | t0006 | g0075 | EAS | JPT | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
NA19062 | hp1 | a0001 | c0001 | t0020 | g0007 | EAS | JPT | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
NA19062 | hp2 | a0001 | c0001 | t0002 | g0187 | EAS | JPT | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
NA19063 | hp1 | a0001 | c0001 | t0002 | g0184 | EAS | JPT | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
NA19063 | hp2 | a0001 | c0001 | t0002 | g0211 | EAS | JPT | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
NA19065 | hp1 | a0001 | c0001 | t0002 | g0165 | EAS | JPT | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
NA19065 | hp2 | a0001 | c0001 | t0001 | g0109 | EAS | JPT | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
NA19066 | hp1 | a0001 | c0001 | t0001 | g0061 | EAS | JPT | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
NA19066 | hp2 | a0001 | c0001 | t0002 | g0200 | EAS | JPT | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
NA19068 | hp1 | a0001 | c0001 | t0001 | g0107 | EAS | JPT | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
NA19068 | hp2 | a0001 | c0001 | t0002 | g0174 | EAS | JPT | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
NA19072 | hp1 | a0001 | c0001 | t0001 | g0122 | EAS | JPT | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
NA19072 | hp2 | a0001 | c0001 | t0002 | g0025 | EAS | JPT | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
NA19074 | hp1 | a0001 | c0001 | t0002 | g0233 | EAS | JPT | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
NA19074 | hp2 | a0001 | c0001 | t0001 | g0108 | EAS | JPT | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
NA19075 | hp1 | a0001 | c0001 | t0001 | g0120 | EAS | JPT | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
NA19075 | hp2 | a0001 | c0001 | t0002 | g0186 | EAS | JPT | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
NA19078 | hp1 | a0001 | c0001 | t0002 | g0237 | EAS | JPT | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
NA19078 | hp2 | a0001 | c0001 | t0006 | g0090 | EAS | JPT | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
NA19080 | hp1 | a0001 | c0001 | t0001 | g0028 | EAS | JPT | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
NA19080 | hp2 | a0001 | c0001 | t0002 | g0232 | EAS | JPT | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
NA19085 | hp1 | a0001 | c0001 | t0002 | g0235 | EAS | JPT | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
NA19085 | hp2 | a0001 | c0001 | t0001 | g0054 | EAS | JPT | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
NA19090 | hp1 | a0001 | c0001 | t0002 | g0180 | EAS | JPT | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
NA19090 | hp2 | a0001 | c0001 | t0001 | g0019 | EAS | JPT | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
NA19240 | hp1 | a0001 | c0001 | t0004 | g0138 | AFR | YRI | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
NA19240 | hp2 | a0003 | c0003 | t0005 | g0040 | AFR | YRI | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
NA20129 | hp1 | a0003 | c0003 | t0005 | g0010 | AFR | ASW | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
NA20129 | hp2 | a0001 | c0001 | t0001 | g0012 | AFR | ASW | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
NA20752 | hp1 | a0001 | c0001 | t0001 | g0008 | EUR | TSI | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
NA20752 | hp2 | a0001 | c0001 | t0002 | g0207 | EUR | TSI | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
NA20805 | hp1 | a0001 | c0001 | t0002 | g0192 | EUR | TSI | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
NA20805 | hp2 | a0002 | c0002 | t0003 | g0149 | EUR | TSI | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
HG02109 | hp1 | a0001 | c0001 | t0003 | g0223 | AFR | ACB | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
HG02109 | hp2 | a0001 | c0001 | t0001 | g0114 | AFR | ACB | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
HG02486 | hp1 | a0003 | c0003 | t0005 | g0010 | AFR | ACB | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
HG02486 | hp2 | a0001 | c0001 | t0004 | g0003 | AFR | ACB | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
HG02559 | hp1 | a0004 | c0004 | t0007 | g0128 | AFR | ACB | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
HG02559 | hp2 | a0001 | c0001 | t0001 | g0071 | AFR | ACB | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
HG03471 | hp1 | a0001 | c0001 | t0001 | g0077 | AFR | MSL | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
HG03471 | hp2 | a0001 | c0001 | t0019 | g0135 | AFR | MSL | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
NA18955 | hp1 | a0001 | c0001 | t0002 | g0168 | EAS | JPT | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
NA18955 | hp2 | a0001 | c0001 | t0001 | g0065 | EAS | JPT | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
NA20300 | hp1 | a0001 | c0001 | t0003 | g0006 | AFR | USA | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
NA20300 | hp2 | a0003 | c0003 | t0005 | g0032 | AFR | USA | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
NA21309 | hp1 | a0001 | c0001 | t0004 | g0139 | AFR | LWK | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
NA21309 | hp2 | a0001 | c0001 | t0001 | g0081 | AFR | LWK | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0004 | g0215 | REF | REF | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
homoSapiens_grch38 | hp1 | a0001 | c0001 | t0001 | g0206 | REF | REF | NDFIP2_chr13_79476155_79561077 | NDFIP2 | chr13 | 79476155 | 79561077 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr13:79481220
|
G | A | 1 | a0005 | 2 | NA18906.hp2 NA19043.hp1 |
missense_variant | MODERATE | c.17G>A | p.Ser6Asn | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 1/8 | 66/4624 | 17/1011 | 6/336 | chr13 | 79481220 | ||
chr13:79481302
|
C | G | 1 | a0004 | 4 | HG01952.hp1 HG02145.hp1 HG02559.hp1 others(1): Show |
missense_variant | MODERATE | c.99C>G | p.Asn33Lys | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 1/8 | 148/4624 | 99/1011 | 33/336 | chr13 | 79481302 | ||
chr13:79520858
|
C | T | 1 | a0003 | 16 | HG01981.hp2 HG02451.hp1 HG02486.hp1 others(13): Show |
missense_variant | MODERATE | c.370C>T | p.Pro124Ser | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 2/8 | 419/4624 | 370/1011 | 124/336 | chr13 | 79520858 | ||
chr13:79520895
|
C | T | 1 | a0002 | 16 | HG00140.hp1 HG00280.hp1 HG00733.hp1 others(13): Show |
missense_variant | MODERATE | c.407C>T | p.Ala136Val | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 2/8 | 456/4624 | 407/1011 | 136/336 | chr13 | 79520895 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr13:79533336
|
C | T | 1 | a0001c0006 | 1 | HG02040.hp2 | synonymous_variant | LOW | c.501C>T | p.Tyr167Tyr | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 3/8 | 550/4624 | 501/1011 | 167/336 | chr13 | 79533336 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr13:79552633
|
G | A | 6 | a0001c0001t0002a0001c0001t0009a0001c0001t0012others(3): Show | 91 | HG00099.hp1 HG00323.hp1 HG00408.hp2 others(88): Show |
3_prime_UTR_variant | MODIFIER | c.*120G>A | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 8/8 | 1513 | chr13 | 79552633 | |||||
chr13:79552645
|
T | G | 3 | a0001c0001t0015a0003c0003t0005a0003c0003t0010 | 17 | HG01981.hp2 HG02451.hp1 HG02486.hp1 others(14): Show |
3_prime_UTR_variant | MODIFIER | c.*132T>G | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 8/8 | 1525 | chr13 | 79552645 | |||||
chr13:79552673
|
A | G | 3 | a0001c0001t0015a0003c0003t0005a0003c0003t0010 | 17 | HG01981.hp2 HG02451.hp1 HG02486.hp1 others(14): Show |
3_prime_UTR_variant | MODIFIER | c.*160A>G | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 8/8 | 1553 | chr13 | 79552673 | |||||
chr13:79553040
|
A | G | 1 | a0001c0001t0021 | 1 | NA18945.hp2 | 3_prime_UTR_variant | MODIFIER | c.*527A>G | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 8/8 | 1920 | chr13 | 79553040 | |||||
chr13:79553117
|
A | C | 1 | a0001c0001t0008 | 3 | HG02723.hp1 HG02886.hp1 HG03579.hp2 |
3_prime_UTR_variant | MODIFIER | c.*604A>C | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 8/8 | 1997 | chr13 | 79553117 | |||||
chr13:79553235
|
C | T | 1 | a0001c0001t0020 | 1 | NA19062.hp1 | 3_prime_UTR_variant | MODIFIER | c.*722C>T | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 8/8 | 2115 | chr13 | 79553235 | |||||
chr13:79553244
|
T | TAA | 3 | a0001c0001t0006a0001c0001t0016a0001c0006t0006 | 10 | HG02040.hp2 HG02074.hp1 HG02129.hp2 others(7): Show |
3_prime_UTR_variant | MODIFIER | c.*733_*734dupAA | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 8/8 | 2128 | INFO_REALIGN_3_PRIME | chr13 | 79553244 | ||||
chr13:79553323
|
A | G | 15 | a0001c0001t0002a0001c0001t0003a0001c0001t0004others(12): Show | 171 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(168): Show |
3_prime_UTR_variant | MODIFIER | c.*810A>G | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 8/8 | 2203 | chr13 | 79553323 | |||||
chr13:79553339
|
T | C | 4 | a0001c0001t0003a0001c0001t0009a0002c0002t0003others(1): Show | 43 | HG00140.hp1 HG00280.hp1 HG00733.hp1 others(40): Show |
3_prime_UTR_variant | MODIFIER | c.*826T>C | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 8/8 | 2219 | chr13 | 79553339 | |||||
chr13:79553500
|
A | G | 5 | a0001c0001t0004a0001c0001t0008a0001c0001t0018others(2): Show | 27 | HG01069.hp1 HG01071.hp1 HG01243.hp2 others(24): Show |
3_prime_UTR_variant | MODIFIER | c.*987A>G | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 8/8 | 2380 | chr13 | 79553500 | |||||
chr13:79553586
|
A | G | 1 | a0001c0001t0014 | 1 | HG00741.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1073A>G | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 8/8 | 2466 | chr13 | 79553586 | |||||
chr13:79553614
|
G | A | 1 | a0003c0003t0010 | 2 | HG02965.hp2 NA18522.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1101G>A | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 8/8 | 2494 | chr13 | 79553614 | |||||
chr13:79554426
|
G | A | 1 | a0001c0001t0016 | 1 | NA19002.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1913G>A | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 8/8 | 3306 | chr13 | 79554426 | |||||
chr13:79554549
|
G | A | 2 | a0003c0003t0005a0003c0003t0010 | 16 | HG01981.hp2 HG02451.hp1 HG02486.hp1 others(13): Show |
3_prime_UTR_variant | MODIFIER | c.*2036G>A | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 8/8 | 3429 | chr13 | 79554549 | |||||
chr13:79554857
|
A | T | 1 | a0001c0001t0013 | 1 | NA18986.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2344A>T | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 8/8 | 3737 | chr13 | 79554857 | |||||
chr13:79554869
|
A | G | 1 | a0001c0001t0011 | 2 | HG01515.hp2 HG01517.hp1 |
3_prime_UTR_variant | MODIFIER | c.*2356A>G | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 8/8 | 3749 | chr13 | 79554869 | |||||
chr13:79555110
|
A | G | 1 | a0001c0001t0012 | 1 | NA18990.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2597A>G | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 8/8 | 3990 | chr13 | 79555110 | |||||
chr13:79555193
|
T | C | 6 | a0001c0001t0002a0001c0001t0009a0001c0001t0012others(3): Show | 91 | HG00099.hp1 HG00323.hp1 HG00408.hp2 others(88): Show |
3_prime_UTR_variant | MODIFIER | c.*2680T>C | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 8/8 | 4073 | chr13 | 79555193 | |||||
chr13:79555391
|
A | C | 1 | a0001c0001t0017 | 1 | NA18979.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2878A>C | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 8/8 | 4271 | chr13 | 79555391 | |||||
chr13:79555476
|
A | G | 1 | a0001c0001t0019 | 1 | HG03471.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2963A>G | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 8/8 | 4356 | chr13 | 79555476 | |||||
chr13:79555615
|
G | A | 1 | a0001c0001t0018 | 1 | HG02809.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3102G>A | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 8/8 | 4495 | chr13 | 79555615 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr13:79481564
|
C | T | 1 | a0001c0001t0006g0243 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.321+40C>T | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 1/7 | chr13 | 79481564 | ||||||
chr13:79481629
|
T | C | 1 | a0001c0001t0001g0027 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.321+105T>C | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 1/7 | chr13 | 79481629 | ||||||
chr13:79481673
|
C | T | 1 | a0001c0001t0001g0242 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.321+149C>T | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 1/7 | chr13 | 79481673 | ||||||
chr13:79481706
|
G | A | 1 | a0001c0001t0001g0028 | 1 | NA19080.hp1 | intron_variant | MODIFIER | c.321+182G>A | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 1/7 | chr13 | 79481706 | ||||||
chr13:79481772
|
G | C | 15 | a0003c0003t0005g0010a0003c0003t0005g0029a0003c0003t0005g0030others(12): Show | 16 | HG01981.hp2 HG02451.hp1 HG02486.hp1 others(13): Show |
intron_variant | MODIFIER | c.321+248G>C | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 1/7 | chr13 | 79481772 | ||||||
chr13:79482165
|
C | T | 8 | a0003c0003t0005g0010a0003c0003t0005g0036a0003c0003t0005g0037others(5): Show | 9 | HG01981.hp2 HG02451.hp1 HG02486.hp1 others(6): Show |
intron_variant | MODIFIER | c.321+641C>T | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 1/7 | chr13 | 79482165 | ||||||
chr13:79482169
|
C | CT | 15 | a0001c0001t0002g0024a0001c0001t0002g0025a0001c0001t0002g0026others(12): Show | 18 | HG00741.hp1 HG01243.hp1 HG02071.hp1 others(15): Show |
intron_variant | MODIFIER | c.321+671dupT | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr13 | 79482169 | |||||
chr13:79482169
|
C | T | 1 | a0001c0001t0003g0241 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.321+645C>T | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 1/7 | chr13 | 79482169 | ||||||
chr13:79482169
|
CT | C | 89 | a0001c0001t0001g0007a0001c0001t0001g0012a0001c0001t0001g0015others(86): Show | 99 | HG00099.hp2 HG00140.hp2 HG00323.hp2 others(96): Show |
intron_variant | MODIFIER | c.321+671delT | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr13 | 79482169 | |||||
chr13:79482169
|
CTT | C | 16 | a0001c0001t0001g0011a0001c0001t0001g0043a0001c0001t0001g0044others(13): Show | 17 | HG00280.hp2 HG01891.hp2 HG01952.hp1 others(14): Show |
intron_variant | MODIFIER | c.321+670_321+671del others(2): Show |
NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr13 | 79482169 | |||||
chr13:79482169
|
CTTTT | C | 8 | a0003c0003t0005g0010a0003c0003t0005g0036a0003c0003t0005g0037others(5): Show | 9 | HG01981.hp2 HG02451.hp1 HG02486.hp1 others(6): Show |
intron_variant | MODIFIER | c.321+668_321+671del others(4): Show |
NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr13 | 79482169 | |||||
chr13:79482169
|
CTTTTTTT | C | 12 | a0002c0002t0003g0021a0002c0002t0003g0022a0002c0002t0003g0145others(9): Show | 14 | HG00140.hp1 HG00280.hp1 HG00733.hp1 others(11): Show |
intron_variant | MODIFIER | c.321+665_321+671del others(7): Show |
NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr13 | 79482169 | |||||
chr13:79482169
|
CTTTTTTT others(4): Show |
C | 1 | a0002c0002t0003g0144 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.321+661_321+671del others(11): Show |
NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr13 | 79482169 | |||||
chr13:79482172
|
T | TC | 4 | a0001c0001t0001g0123a0001c0001t0001g0124a0001c0001t0001g0125others(1): Show | 4 | HG00735.hp1 HG01192.hp1 HG01261.hp2 others(1): Show |
intron_variant | MODIFIER | c.321+648_321+649ins others(1): Show |
NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 1/7 | chr13 | 79482172 | ||||||
chr13:79482173
|
T | C | 14 | a0001c0001t0001g0008a0001c0001t0001g0111a0001c0001t0001g0112others(11): Show | 16 | HG00738.hp2 HG01074.hp2 HG01496.hp1 others(13): Show |
intron_variant | MODIFIER | c.321+649T>C | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 1/7 | chr13 | 79482173 | ||||||
chr13:79482174
|
T | C | 78 | a0001c0001t0001g0007a0001c0001t0001g0012a0001c0001t0001g0015others(75): Show | 87 | HG00099.hp2 HG00140.hp2 HG00323.hp2 others(84): Show |
intron_variant | MODIFIER | c.321+650T>C | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 1/7 | chr13 | 79482174 | ||||||
chr13:79482175
|
T | C | 4 | a0001c0001t0001g0011a0001c0001t0001g0043a0001c0001t0001g0044others(1): Show | 5 | HG00280.hp2 HG03017.hp2 HG03239.hp2 others(2): Show |
intron_variant | MODIFIER | c.321+651T>C | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 1/7 | chr13 | 79482175 | ||||||
chr13:79482176
|
T | C | 3 | a0001c0001t0004g0003a0001c0001t0004g0142a0001c0001t0004g0143 | 6 | HG02486.hp2 HG02622.hp1 HG03041.hp2 others(3): Show |
intron_variant | MODIFIER | c.321+652T>C | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 1/7 | chr13 | 79482176 | ||||||
chr13:79482177
|
T | C | 6 | a0001c0001t0004g0020a0001c0001t0004g0138a0001c0001t0004g0139others(3): Show | 7 | HG01243.hp2 HG02145.hp1 HG02809.hp1 others(4): Show |
intron_variant | MODIFIER | c.321+653T>C | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 1/7 | chr13 | 79482177 | ||||||
chr13:79482178
|
T | C | 10 | a0001c0001t0004g0133a0001c0001t0004g0134a0001c0001t0004g0136others(7): Show | 10 | HG01891.hp2 HG01952.hp1 HG02559.hp1 others(7): Show |
intron_variant | MODIFIER | c.321+654T>C | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 1/7 | chr13 | 79482178 | ||||||
chr13:79482309
|
A | G | 1 | a0003c0003t0005g0029 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.321+785A>G | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 1/7 | chr13 | 79482309 | ||||||
chr13:79482366
|
T | C | 102 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0011others(99): Show | 114 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(111): Show |
intron_variant | MODIFIER | c.321+842T>C | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 1/7 | chr13 | 79482366 | ||||||
chr13:79482451
|
C | G | 25 | a0001c0001t0001g0011a0001c0001t0001g0016a0001c0001t0001g0017others(22): Show | 30 | HG00280.hp2 HG00544.hp1 HG01258.hp1 others(27): Show |
intron_variant | MODIFIER | c.321+927C>G | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 1/7 | chr13 | 79482451 | ||||||
chr13:79482497
|
A | G | 1 | a0001c0001t0001g0120 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.321+973A>G | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 1/7 | chr13 | 79482497 | ||||||
chr13:79482630
|
AG | A | 170 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0011others(167): Show | 194 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(191): Show |
intron_variant | MODIFIER | c.321+1108delG | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr13 | 79482630 | |||||
chr13:79482772
|
C | T | 172 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0011others(169): Show | 196 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(193): Show |
intron_variant | MODIFIER | c.321+1248C>T | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 1/7 | chr13 | 79482772 | ||||||
chr13:79482831
|
A | G | 1 | a0001c0001t0001g0242 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.321+1307A>G | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 1/7 | chr13 | 79482831 | ||||||
chr13:79483178
|
A | G | 1 | a0001c0001t0002g0240 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.321+1654A>G | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 1/7 | chr13 | 79483178 | ||||||
chr13:79483546
|
A | C | 32 | a0001c0001t0003g0006a0001c0001t0003g0158a0001c0001t0003g0159others(29): Show | 37 | HG00140.hp1 HG00280.hp1 HG00733.hp1 others(34): Show |
intron_variant | MODIFIER | c.321+2022A>C | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 1/7 | chr13 | 79483546 | ||||||
chr13:79483696
|
C | T | 25 | a0001c0001t0001g0011a0001c0001t0001g0016a0001c0001t0001g0017others(22): Show | 30 | HG00280.hp2 HG00544.hp1 HG01258.hp1 others(27): Show |
intron_variant | MODIFIER | c.321+2172C>T | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 1/7 | chr13 | 79483696 | ||||||
chr13:79483704
|
G | T | 36 | a0001c0001t0004g0003a0001c0001t0004g0009a0001c0001t0004g0020others(33): Show | 43 | HG01069.hp1 HG01071.hp1 HG01243.hp2 others(40): Show |
intron_variant | MODIFIER | c.321+2180G>T | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 1/7 | chr13 | 79483704 | ||||||
chr13:79483744
|
A | C | 2 | a0003c0003t0010g0034a0003c0003t0010g0035 | 2 | HG02965.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.321+2220A>C | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 1/7 | chr13 | 79483744 | ||||||
chr13:79483820
|
A | G | 15 | a0003c0003t0005g0010a0003c0003t0005g0029a0003c0003t0005g0030others(12): Show | 16 | HG01981.hp2 HG02451.hp1 HG02486.hp1 others(13): Show |
intron_variant | MODIFIER | c.321+2296A>G | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 1/7 | chr13 | 79483820 | ||||||
chr13:79483859
|
T | C | 2 | a0005c0005t0002g0155a0005c0005t0002g0157 | 2 | NA18906.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.321+2335T>C | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 1/7 | chr13 | 79483859 | ||||||
chr13:79483947
|
C | T | 2 | a0003c0003t0010g0034a0003c0003t0010g0035 | 2 | HG02965.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.321+2423C>T | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 1/7 | chr13 | 79483947 | ||||||
chr13:79484101
|
C | T | 1 | a0002c0002t0003g0154 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.321+2577C>T | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 1/7 | chr13 | 79484101 | ||||||
chr13:79484173
|
A | G | 36 | a0001c0001t0004g0003a0001c0001t0004g0009a0001c0001t0004g0020others(33): Show | 43 | HG01069.hp1 HG01071.hp1 HG01243.hp2 others(40): Show |
intron_variant | MODIFIER | c.321+2649A>G | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 1/7 | chr13 | 79484173 | ||||||
chr13:79484187
|
T | C | 2 | a0005c0005t0002g0155a0005c0005t0002g0157 | 2 | NA18906.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.321+2663T>C | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 1/7 | chr13 | 79484187 | ||||||
chr13:79484339
|
T | C | 13 | a0003c0003t0005g0010a0003c0003t0005g0029a0003c0003t0005g0030others(10): Show | 14 | HG01981.hp2 HG02451.hp1 HG02486.hp1 others(11): Show |
intron_variant | MODIFIER | c.321+2815T>C | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 1/7 | chr13 | 79484339 | ||||||
chr13:79484372
|
C | T | 4 | a0001c0001t0003g0006a0001c0001t0003g0161a0001c0001t0003g0227others(1): Show | 7 | HG02257.hp2 HG02572.hp2 HG02922.hp2 others(4): Show |
intron_variant | MODIFIER | c.321+2848C>T | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 1/7 | chr13 | 79484372 | ||||||
chr13:79484654
|
A | T | 12 | a0003c0003t0005g0010a0003c0003t0005g0030a0003c0003t0005g0031others(9): Show | 13 | HG01981.hp2 HG02451.hp1 HG02486.hp1 others(10): Show |
intron_variant | MODIFIER | c.321+3130A>T | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 1/7 | chr13 | 79484654 | ||||||
chr13:79484797
|
G | T | 1 | a0001c0001t0009g0239 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.321+3273G>T | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 1/7 | chr13 | 79484797 | ||||||
chr13:79484945
|
C | T | 102 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0011others(99): Show | 114 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(111): Show |
intron_variant | MODIFIER | c.321+3421C>T | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 1/7 | chr13 | 79484945 | ||||||
chr13:79484963
|
G | A | 2 | a0001c0001t0001g0012a0001c0001t0001g0046 | 3 | HG02630.hp2 HG03486.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.321+3439G>A | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 1/7 | chr13 | 79484963 | ||||||
chr13:79485076
|
C | T | 2 | a0001c0001t0002g0214a0001c0001t0002g0238 | 2 | NA18990.hp2 NA18991.hp1 |
intron_variant | MODIFIER | c.321+3552C>T | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 1/7 | chr13 | 79485076 | ||||||
chr13:79485420
|
T | C | 15 | a0003c0003t0005g0010a0003c0003t0005g0029a0003c0003t0005g0030others(12): Show | 16 | HG01981.hp2 HG02451.hp1 HG02486.hp1 others(13): Show |
intron_variant | MODIFIER | c.321+3896T>C | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 1/7 | chr13 | 79485420 | ||||||
chr13:79485461
|
G | C | 1 | a0001c0001t0002g0229 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.321+3937G>C | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 1/7 | chr13 | 79485461 | ||||||
chr13:79485488
|
A | T | 15 | a0003c0003t0005g0010a0003c0003t0005g0029a0003c0003t0005g0030others(12): Show | 16 | HG01981.hp2 HG02451.hp1 HG02486.hp1 others(13): Show |
intron_variant | MODIFIER | c.321+3964A>T | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 1/7 | chr13 | 79485488 | ||||||
chr13:79485716
|
T | A | 1 | a0001c0001t0002g0164 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.321+4192T>A | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 1/7 | chr13 | 79485716 | ||||||
chr13:79485743
|
C | T | 21 | a0001c0001t0004g0003a0001c0001t0004g0009a0001c0001t0004g0020others(18): Show | 27 | HG01069.hp1 HG01071.hp1 HG01243.hp2 others(24): Show |
intron_variant | MODIFIER | c.321+4219C>T | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 1/7 | chr13 | 79485743 | ||||||
chr13:79485976
|
A | T | 2 | a0003c0003t0010g0034a0003c0003t0010g0035 | 2 | HG02965.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.321+4452A>T | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 1/7 | chr13 | 79485976 | ||||||
chr13:79486111
|
C | T | 1 | a0001c0001t0001g0119 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.321+4587C>T | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 1/7 | chr13 | 79486111 | ||||||
chr13:79486334
|
G | A | 1 | a0004c0004t0007g0127 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.321+4810G>A | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 1/7 | chr13 | 79486334 | ||||||
chr13:79486341
|
A | G | 1 | a0001c0001t0002g0213 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.321+4817A>G | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 1/7 | chr13 | 79486341 | ||||||
chr13:79486391
|
A | G | 1 | a0001c0001t0003g0226 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.321+4867A>G | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 1/7 | chr13 | 79486391 | ||||||
chr13:79486552
|
A | G | 170 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0011others(167): Show | 194 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(191): Show |
intron_variant | MODIFIER | c.321+5028A>G | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 1/7 | chr13 | 79486552 | ||||||
chr13:79486572
|
G | A | 12 | a0001c0001t0003g0006a0001c0001t0003g0158a0001c0001t0003g0159others(9): Show | 15 | HG00735.hp2 HG01884.hp2 HG02055.hp1 others(12): Show |
intron_variant | MODIFIER | c.321+5048G>A | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 1/7 | chr13 | 79486572 | ||||||
chr13:79486579
|
T | C | 2 | a0001c0001t0001g0047a0001c0001t0001g0048 | 2 | HG03834.hp1 HG04228.hp2 |
intron_variant | MODIFIER | c.321+5055T>C | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 1/7 | chr13 | 79486579 | ||||||
chr13:79486669
|
G | A | 2 | a0003c0003t0010g0034a0003c0003t0010g0035 | 2 | HG02965.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.321+5145G>A | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 1/7 | chr13 | 79486669 | ||||||
chr13:79486727
|
G | T | 2 | a0003c0003t0010g0034a0003c0003t0010g0035 | 2 | HG02965.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.321+5203G>T | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 1/7 | chr13 | 79486727 | ||||||
chr13:79486728
|
T | C | 1 | a0001c0001t0002g0165 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.321+5204T>C | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 1/7 | chr13 | 79486728 | ||||||
chr13:79486741
|
T | C | 1 | a0003c0003t0010g0034 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.321+5217T>C | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 1/7 | chr13 | 79486741 | ||||||
chr13:79486767
|
A | G | 1 | a0002c0002t0003g0153 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.321+5243A>G | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 1/7 | chr13 | 79486767 | ||||||
chr13:79486856
|
G | A | 1 | a0001c0001t0001g0096 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.321+5332G>A | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 1/7 | chr13 | 79486856 | ||||||
chr13:79486939
|
T | C | 172 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0011others(169): Show | 196 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(193): Show |
intron_variant | MODIFIER | c.321+5415T>C | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 1/7 | chr13 | 79486939 | ||||||
chr13:79487028
|
T | A | 1 | a0002c0002t0003g0021 | 2 | HG03490.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.321+5504T>A | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 1/7 | chr13 | 79487028 | ||||||
chr13:79487044
|
A | G | 2 | a0001c0001t0003g0224a0001c0001t0003g0225 | 2 | HG03017.hp1 NA18939.hp2 |
intron_variant | MODIFIER | c.321+5520A>G | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 1/7 | chr13 | 79487044 | ||||||
chr13:79487233
|
T | G | 1 | a0001c0001t0002g0166 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.321+5709T>G | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 1/7 | chr13 | 79487233 | ||||||
chr13:79487322
|
A | G | 15 | a0003c0003t0005g0010a0003c0003t0005g0029a0003c0003t0005g0030others(12): Show | 16 | HG01981.hp2 HG02451.hp1 HG02486.hp1 others(13): Show |
intron_variant | MODIFIER | c.321+5798A>G | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 1/7 | chr13 | 79487322 | ||||||
chr13:79487352
|
C | T | 3 | a0001c0001t0002g0210a0001c0001t0002g0211a0001c0001t0002g0212 | 3 | NA18969.hp2 NA19006.hp2 NA19063.hp2 |
intron_variant | MODIFIER | c.321+5828C>T | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 1/7 | chr13 | 79487352 | ||||||
chr13:79487372
|
A | C | 102 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0011others(99): Show | 114 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(111): Show |
intron_variant | MODIFIER | c.321+5848A>C | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 1/7 | chr13 | 79487372 | ||||||
chr13:79487440
|
G | A | 1 | a0003c0003t0005g0029 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.321+5916G>A | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 1/7 | chr13 | 79487440 | ||||||
chr13:79487453
|
G | T | 15 | a0003c0003t0005g0010a0003c0003t0005g0029a0003c0003t0005g0030others(12): Show | 16 | HG01981.hp2 HG02451.hp1 HG02486.hp1 others(13): Show |
intron_variant | MODIFIER | c.321+5929G>T | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 1/7 | chr13 | 79487453 | ||||||
chr13:79487487
|
C | A | 2 | a0001c0001t0001g0049a0001c0001t0001g0050 | 2 | HG02698.hp2 HG03654.hp1 |
intron_variant | MODIFIER | c.321+5963C>A | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 1/7 | chr13 | 79487487 | ||||||
chr13:79487594
|
T | C | 1 | a0001c0001t0018g0137 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.321+6070T>C | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 1/7 | chr13 | 79487594 | ||||||
chr13:79487702
|
C | T | 3 | a0001c0001t0002g0208a0001c0001t0009g0209a0001c0001t0009g0239 | 3 | HG01243.hp1 HG02055.hp2 HG02300.hp2 |
intron_variant | MODIFIER | c.321+6178C>T | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 1/7 | chr13 | 79487702 | ||||||
chr13:79487785
|
G | C | 1 | a0004c0004t0007g0128 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.321+6261G>C | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 1/7 | chr13 | 79487785 | ||||||
chr13:79487882
|
T | C | 29 | a0001c0001t0002g0004a0001c0001t0002g0005a0001c0001t0002g0024others(26): Show | 36 | HG00099.hp1 HG00323.hp1 HG00408.hp2 others(33): Show |
intron_variant | MODIFIER | c.321+6358T>C | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 1/7 | chr13 | 79487882 | ||||||
chr13:79488140
|
G | GA | 21 | a0001c0001t0004g0003a0001c0001t0004g0009a0001c0001t0004g0020others(18): Show | 27 | HG01069.hp1 HG01071.hp1 HG01243.hp2 others(24): Show |
intron_variant | MODIFIER | c.321+6622dupA | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr13 | 79488140 | |||||
chr13:79488210
|
A | G | 1 | a0003c0003t0005g0033 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.321+6686A>G | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 1/7 | chr13 | 79488210 | ||||||
chr13:79488364
|
G | A | 1 | a0003c0003t0005g0029 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.321+6840G>A | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 1/7 | chr13 | 79488364 | ||||||
chr13:79488465
|
G | C | 7 | a0001c0001t0003g0158a0001c0001t0003g0159a0001c0001t0003g0216others(4): Show | 7 | HG00735.hp2 HG01884.hp2 HG02145.hp2 others(4): Show |
intron_variant | MODIFIER | c.321+6941G>C | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 1/7 | chr13 | 79488465 | ||||||
chr13:79488631
|
T | A | 102 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0011others(99): Show | 114 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(111): Show |
intron_variant | MODIFIER | c.321+7107T>A | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 1/7 | chr13 | 79488631 | ||||||
chr13:79488941
|
T | G | 2 | a0001c0001t0002g0168a0001c0001t0013g0167 | 2 | NA18955.hp1 NA18986.hp2 |
intron_variant | MODIFIER | c.321+7417T>G | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 1/7 | chr13 | 79488941 | ||||||
chr13:79489344
|
C | T | 21 | a0001c0001t0004g0003a0001c0001t0004g0009a0001c0001t0004g0020others(18): Show | 27 | HG01069.hp1 HG01071.hp1 HG01243.hp2 others(24): Show |
intron_variant | MODIFIER | c.321+7820C>T | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 1/7 | chr13 | 79489344 | ||||||
chr13:79489412
|
A | G | 12 | a0001c0001t0003g0006a0001c0001t0003g0158a0001c0001t0003g0159others(9): Show | 15 | HG00735.hp2 HG01884.hp2 HG02055.hp1 others(12): Show |
intron_variant | MODIFIER | c.321+7888A>G | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 1/7 | chr13 | 79489412 | ||||||
chr13:79489641
|
C | T | 1 | a0001c0001t0002g0207 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.321+8117C>T | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 1/7 | chr13 | 79489641 | ||||||
chr13:79489780
|
G | T | 12 | a0001c0001t0003g0006a0001c0001t0003g0158a0001c0001t0003g0159others(9): Show | 15 | HG00735.hp2 HG01884.hp2 HG02055.hp1 others(12): Show |
intron_variant | MODIFIER | c.321+8256G>T | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 1/7 | chr13 | 79489780 | ||||||
chr13:79489962
|
A | G | 1 | a0003c0003t0005g0029 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.321+8438A>G | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 1/7 | chr13 | 79489962 | ||||||
chr13:79489967
|
C | T | 1 | a0001c0001t0001g0095 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.321+8443C>T | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 1/7 | chr13 | 79489967 | ||||||
chr13:79490000
|
G | A | 170 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0011others(167): Show | 194 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(191): Show |
intron_variant | MODIFIER | c.321+8476G>A | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 1/7 | chr13 | 79490000 | ||||||
chr13:79490018
|
A | T | 1 | a0001c0001t0001g0118 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.321+8494A>T | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 1/7 | chr13 | 79490018 | ||||||
chr13:79490269
|
A | G | 1 | a0001c0001t0017g0094 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.321+8745A>G | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 1/7 | chr13 | 79490269 | ||||||
chr13:79490289
|
C | T | 2 | a0003c0003t0010g0034a0003c0003t0010g0035 | 2 | HG02965.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.321+8765C>T | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 1/7 | chr13 | 79490289 | ||||||
chr13:79490322
|
A | G | 3 | a0001c0001t0004g0134a0001c0001t0004g0136a0001c0001t0019g0135 | 3 | HG02572.hp1 HG02615.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.321+8798A>G | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 1/7 | chr13 | 79490322 | ||||||
chr13:79490379
|
T | C | 244 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0011others(241): Show | 285 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(282): Show |
intron_variant | MODIFIER | c.321+8855T>C | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 1/7 | chr13 | 79490379 | ||||||
chr13:79490472
|
T | C | 1 | a0001c0001t0001g0097 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.321+8948T>C | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 1/7 | chr13 | 79490472 | ||||||
chr13:79490645
|
T | A | 1 | a0001c0001t0001g0119 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.321+9121T>A | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 1/7 | chr13 | 79490645 | ||||||
chr13:79490646
|
G | A | 1 | a0001c0001t0001g0119 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.321+9122G>A | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 1/7 | chr13 | 79490646 | ||||||
chr13:79490647
|
G | A | 1 | a0001c0001t0001g0119 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.321+9123G>A | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 1/7 | chr13 | 79490647 | ||||||
chr13:79490649
|
T | C | 1 | a0001c0001t0001g0119 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.321+9125T>C | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 1/7 | chr13 | 79490649 | ||||||
chr13:79490651
|
T | A | 1 | a0001c0001t0001g0119 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.321+9127T>A | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 1/7 | chr13 | 79490651 | ||||||
chr13:79490756
|
T | A | 2 | a0001c0001t0002g0023a0001c0001t0002g0184 | 3 | NA18982.hp2 NA19060.hp1 NA19063.hp1 |
intron_variant | MODIFIER | c.321+9232T>A | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 1/7 | chr13 | 79490756 | ||||||
chr13:79490895
|
A | C | 2 | a0001c0001t0002g0182a0001c0001t0002g0183 | 2 | HG00544.hp2 HG02074.hp2 |
intron_variant | MODIFIER | c.321+9371A>C | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 1/7 | chr13 | 79490895 | ||||||
chr13:79491422
|
GTC | G | 15 | a0003c0003t0005g0010a0003c0003t0005g0029a0003c0003t0005g0030others(12): Show | 16 | HG01981.hp2 HG02451.hp1 HG02486.hp1 others(13): Show |
intron_variant | MODIFIER | c.321+9908_321+9909d others(4): Show |
NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr13 | 79491422 | |||||
chr13:79491514
|
C | T | 2 | a0003c0003t0010g0034a0003c0003t0010g0035 | 2 | HG02965.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.321+9990C>T | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 1/7 | chr13 | 79491514 | ||||||
chr13:79491643
|
G | A | 21 | a0001c0001t0004g0003a0001c0001t0004g0009a0001c0001t0004g0020others(18): Show | 27 | HG01069.hp1 HG01071.hp1 HG01243.hp2 others(24): Show |
intron_variant | MODIFIER | c.321+10119G>A | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 1/7 | chr13 | 79491643 | ||||||
chr13:79492033
|
G | C | 3 | a0001c0001t0002g0169a0001c0001t0002g0170a0001c0001t0002g0230 | 3 | HG00741.hp1 HG03688.hp1 HG03831.hp1 |
intron_variant | MODIFIER | c.321+10509G>C | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 1/7 | chr13 | 79492033 | ||||||
chr13:79492171
|
T | C | 15 | a0003c0003t0005g0010a0003c0003t0005g0029a0003c0003t0005g0030others(12): Show | 16 | HG01981.hp2 HG02451.hp1 HG02486.hp1 others(13): Show |
intron_variant | MODIFIER | c.321+10647T>C | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 1/7 | chr13 | 79492171 | ||||||
chr13:79492184
|
A | T | 1 | a0002c0002t0003g0154 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.321+10660A>T | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 1/7 | chr13 | 79492184 | ||||||
chr13:79492213
|
C | T | 12 | a0001c0001t0003g0006a0001c0001t0003g0158a0001c0001t0003g0159others(9): Show | 15 | HG00735.hp2 HG01884.hp2 HG02055.hp1 others(12): Show |
intron_variant | MODIFIER | c.321+10689C>T | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 1/7 | chr13 | 79492213 | ||||||
chr13:79492244
|
AGT | A | 2 | a0002c0002t0003g0021a0002c0002t0003g0144 | 3 | HG02698.hp1 HG03490.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.321+10722_321+1072 others(6): Show |
NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr13 | 79492244 | |||||
chr13:79492252
|
C | CT | 6 | a0001c0001t0001g0093a0001c0001t0001g0117a0001c0001t0001g0125others(3): Show | 6 | HG00735.hp1 HG01891.hp1 HG02145.hp1 others(3): Show |
intron_variant | MODIFIER | c.321+10745dupT | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr13 | 79492252 | |||||
chr13:79492252
|
CT | C | 5 | a0001c0001t0001g0012a0001c0001t0001g0046a0001c0001t0001g0051others(2): Show | 6 | HG02630.hp2 HG02922.hp1 HG03225.hp1 others(3): Show |
intron_variant | MODIFIER | c.321+10745delT | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr13 | 79492252 | |||||
chr13:79492323
|
C | T | 1 | a0001c0001t0003g0223 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.321+10799C>T | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 1/7 | chr13 | 79492323 | ||||||
chr13:79492435
|
G | A | 1 | a0003c0003t0005g0029 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.321+10911G>A | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 1/7 | chr13 | 79492435 | ||||||
chr13:79492487
|
T | C | 15 | a0003c0003t0005g0010a0003c0003t0005g0029a0003c0003t0005g0030others(12): Show | 16 | HG01981.hp2 HG02451.hp1 HG02486.hp1 others(13): Show |
intron_variant | MODIFIER | c.321+10963T>C | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 1/7 | chr13 | 79492487 | ||||||
chr13:79492531
|
A | G | 32 | a0001c0001t0003g0006a0001c0001t0003g0158a0001c0001t0003g0159others(29): Show | 37 | HG00140.hp1 HG00280.hp1 HG00733.hp1 others(34): Show |
intron_variant | MODIFIER | c.321+11007A>G | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 1/7 | chr13 | 79492531 | ||||||
chr13:79492566
|
T | C | 1 | a0001c0001t0004g0138 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.321+11042T>C | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 1/7 | chr13 | 79492566 | ||||||
chr13:79492641
|
T | C | 170 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0011others(167): Show | 194 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(191): Show |
intron_variant | MODIFIER | c.321+11117T>C | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 1/7 | chr13 | 79492641 | ||||||
chr13:79492867
|
A | G | 1 | a0001c0001t0002g0205 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.321+11343A>G | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 1/7 | chr13 | 79492867 | ||||||
chr13:79492868
|
T | C | 15 | a0003c0003t0005g0010a0003c0003t0005g0029a0003c0003t0005g0030others(12): Show | 16 | HG01981.hp2 HG02451.hp1 HG02486.hp1 others(13): Show |
intron_variant | MODIFIER | c.321+11344T>C | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 1/7 | chr13 | 79492868 | ||||||
chr13:79493105
|
G | T | 1 | a0001c0001t0002g0204 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.321+11581G>T | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 1/7 | chr13 | 79493105 | ||||||
chr13:79493209
|
T | C | 2 | a0001c0001t0002g0023a0001c0001t0002g0184 | 3 | NA18982.hp2 NA19060.hp1 NA19063.hp1 |
intron_variant | MODIFIER | c.321+11685T>C | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 1/7 | chr13 | 79493209 | ||||||
chr13:79493242
|
G | A | 15 | a0003c0003t0005g0010a0003c0003t0005g0029a0003c0003t0005g0030others(12): Show | 16 | HG01981.hp2 HG02451.hp1 HG02486.hp1 others(13): Show |
intron_variant | MODIFIER | c.321+11718G>A | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 1/7 | chr13 | 79493242 | ||||||
chr13:79493251
|
A | G | 1 | a0001c0001t0001g0119 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.321+11727A>G | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 1/7 | chr13 | 79493251 | ||||||
chr13:79493467
|
A | G | 1 | a0001c0001t0006g0092 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.321+11943A>G | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 1/7 | chr13 | 79493467 | ||||||
chr13:79493596
|
C | T | 1 | a0001c0001t0001g0091 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.321+12072C>T | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 1/7 | chr13 | 79493596 | ||||||
chr13:79493708
|
A | G | 1 | a0003c0003t0005g0029 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.321+12184A>G | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 1/7 | chr13 | 79493708 | ||||||
chr13:79493853
|
A | T | 1 | a0001c0001t0002g0237 | 1 | NA19078.hp1 | intron_variant | MODIFIER | c.321+12329A>T | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 1/7 | chr13 | 79493853 | ||||||
chr13:79493871
|
T | C | 12 | a0001c0001t0003g0006a0001c0001t0003g0158a0001c0001t0003g0159others(9): Show | 15 | HG00735.hp2 HG01884.hp2 HG02055.hp1 others(12): Show |
intron_variant | MODIFIER | c.321+12347T>C | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 1/7 | chr13 | 79493871 | ||||||
chr13:79493941
|
C | T | 2 | a0003c0003t0010g0034a0003c0003t0010g0035 | 2 | HG02965.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.321+12417C>T | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 1/7 | chr13 | 79493941 | ||||||
chr13:79494433
|
T | G | 15 | a0003c0003t0005g0010a0003c0003t0005g0029a0003c0003t0005g0030others(12): Show | 16 | HG01981.hp2 HG02451.hp1 HG02486.hp1 others(13): Show |
intron_variant | MODIFIER | c.321+12909T>G | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 1/7 | chr13 | 79494433 | ||||||
chr13:79494531
|
G | A | 1 | a0001c0001t0003g0224 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.321+13007G>A | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 1/7 | chr13 | 79494531 | ||||||
chr13:79494666
|
T | C | 1 | a0001c0001t0003g0221 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.321+13142T>C | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 1/7 | chr13 | 79494666 | ||||||
chr13:79494730
|
A | T | 2 | a0001c0001t0002g0166a0001c0001t0002g0180 | 2 | NA18962.hp1 NA19090.hp1 |
intron_variant | MODIFIER | c.321+13206A>T | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 1/7 | chr13 | 79494730 | ||||||
chr13:79494922
|
A | G | 15 | a0003c0003t0005g0010a0003c0003t0005g0029a0003c0003t0005g0030others(12): Show | 16 | HG01981.hp2 HG02451.hp1 HG02486.hp1 others(13): Show |
intron_variant | MODIFIER | c.321+13398A>G | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 1/7 | chr13 | 79494922 | ||||||
chr13:79494947
|
A | G | 1 | a0001c0001t0001g0163 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.321+13423A>G | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 1/7 | chr13 | 79494947 | ||||||
chr13:79495453
|
T | G | 15 | a0003c0003t0005g0010a0003c0003t0005g0029a0003c0003t0005g0030others(12): Show | 16 | HG01981.hp2 HG02451.hp1 HG02486.hp1 others(13): Show |
intron_variant | MODIFIER | c.321+13929T>G | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 1/7 | chr13 | 79495453 | ||||||
chr13:79495454
|
T | C | 15 | a0003c0003t0005g0010a0003c0003t0005g0029a0003c0003t0005g0030others(12): Show | 16 | HG01981.hp2 HG02451.hp1 HG02486.hp1 others(13): Show |
intron_variant | MODIFIER | c.321+13930T>C | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 1/7 | chr13 | 79495454 | ||||||
chr13:79495546
|
G | T | 32 | a0001c0001t0003g0006a0001c0001t0003g0158a0001c0001t0003g0159others(29): Show | 37 | HG00140.hp1 HG00280.hp1 HG00733.hp1 others(34): Show |
intron_variant | MODIFIER | c.321+14022G>T | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 1/7 | chr13 | 79495546 | ||||||
chr13:79495832
|
A | G | 2 | a0003c0003t0010g0034a0003c0003t0010g0035 | 2 | HG02965.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.321+14308A>G | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 1/7 | chr13 | 79495832 | ||||||
chr13:79495852
|
CT | C | 3 | a0001c0001t0001g0012a0001c0001t0001g0046a0001c0001t0001g0051 | 4 | HG02630.hp2 HG02922.hp1 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.321+14331delT | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr13 | 79495852 | |||||
chr13:79495943
|
A | C | 2 | a0003c0003t0010g0034a0003c0003t0010g0035 | 2 | HG02965.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.321+14419A>C | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 1/7 | chr13 | 79495943 | ||||||
chr13:79496097
|
C | A | 1 | a0001c0001t0002g0171 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.321+14573C>A | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 1/7 | chr13 | 79496097 | ||||||
chr13:79496144
|
T | C | 1 | a0001c0001t0001g0049 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.321+14620T>C | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 1/7 | chr13 | 79496144 | ||||||
chr13:79496152
|
G | T | 14 | a0002c0002t0003g0021a0002c0002t0003g0022a0002c0002t0003g0144others(11): Show | 16 | HG00140.hp1 HG00280.hp1 HG00733.hp1 others(13): Show |
intron_variant | MODIFIER | c.321+14628G>T | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 1/7 | chr13 | 79496152 | ||||||
chr13:79496307
|
A | G | 1 | a0001c0001t0003g0241 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.321+14783A>G | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 1/7 | chr13 | 79496307 | ||||||
chr13:79496672
|
T | TA | 96 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0011others(93): Show | 107 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(104): Show |
intron_variant | MODIFIER | c.321+15156dupA | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr13 | 79496672 | |||||
chr13:79496860
|
C | T | 1 | a0001c0001t0003g0161 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.321+15336C>T | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 1/7 | chr13 | 79496860 | ||||||
chr13:79496925
|
T | G | 2 | a0003c0003t0010g0034a0003c0003t0010g0035 | 2 | HG02965.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.321+15401T>G | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 1/7 | chr13 | 79496925 | ||||||
chr13:79496939
|
G | A | 2 | a0003c0003t0010g0034a0003c0003t0010g0035 | 2 | HG02965.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.321+15415G>A | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 1/7 | chr13 | 79496939 | ||||||
chr13:79496952
|
A | G | 15 | a0003c0003t0005g0010a0003c0003t0005g0029a0003c0003t0005g0030others(12): Show | 16 | HG01981.hp2 HG02451.hp1 HG02486.hp1 others(13): Show |
intron_variant | MODIFIER | c.321+15428A>G | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 1/7 | chr13 | 79496952 | ||||||
chr13:79497159
|
A | G | 1 | a0003c0003t0005g0029 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.321+15635A>G | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 1/7 | chr13 | 79497159 | ||||||
chr13:79497199
|
T | C | 15 | a0003c0003t0005g0010a0003c0003t0005g0029a0003c0003t0005g0030others(12): Show | 16 | HG01981.hp2 HG02451.hp1 HG02486.hp1 others(13): Show |
intron_variant | MODIFIER | c.321+15675T>C | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 1/7 | chr13 | 79497199 | ||||||
chr13:79497316
|
G | T | 2 | a0001c0001t0001g0015a0001c0001t0011g0014 | 4 | HG00733.hp2 HG00738.hp1 HG01515.hp2 others(1): Show |
intron_variant | MODIFIER | c.321+15792G>T | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 1/7 | chr13 | 79497316 | ||||||
chr13:79497414
|
C | T | 15 | a0003c0003t0005g0010a0003c0003t0005g0029a0003c0003t0005g0030others(12): Show | 16 | HG01981.hp2 HG02451.hp1 HG02486.hp1 others(13): Show |
intron_variant | MODIFIER | c.321+15890C>T | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 1/7 | chr13 | 79497414 | ||||||
chr13:79497484
|
T | C | 36 | a0001c0001t0004g0003a0001c0001t0004g0009a0001c0001t0004g0020others(33): Show | 43 | HG01069.hp1 HG01071.hp1 HG01243.hp2 others(40): Show |
intron_variant | MODIFIER | c.321+15960T>C | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 1/7 | chr13 | 79497484 | ||||||
chr13:79497660
|
G | GT | 26 | a0001c0001t0001g0088a0001c0001t0001g0089a0001c0001t0002g0026others(23): Show | 31 | HG00099.hp2 HG01243.hp2 HG01256.hp1 others(28): Show |
intron_variant | MODIFIER | c.321+16153dupT | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr13 | 79497660 | |||||
chr13:79497660
|
G | GTT | 4 | a0001c0001t0004g0009a0001c0001t0004g0133a0001c0001t0004g0215others(1): Show | 6 | HG01069.hp1 HG01071.hp1 HG01515.hp1 others(3): Show |
intron_variant | MODIFIER | c.321+16152_321+1615 others(6): Show |
NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr13 | 79497660 | |||||
chr13:79497660
|
GT | G | 14 | a0001c0001t0001g0012a0001c0001t0001g0046a0001c0001t0001g0051others(11): Show | 15 | HG02080.hp1 HG02622.hp2 HG02630.hp2 others(12): Show |
intron_variant | MODIFIER | c.321+16153delT | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr13 | 79497660 | |||||
chr13:79497677
|
T | C | 18 | a0001c0001t0003g0006a0001c0001t0003g0158a0001c0001t0003g0159others(15): Show | 21 | HG00735.hp2 HG01884.hp2 HG02055.hp1 others(18): Show |
intron_variant | MODIFIER | c.321+16153T>C | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 1/7 | chr13 | 79497677 | ||||||
chr13:79497677
|
T | TC | 13 | a0002c0002t0003g0021a0002c0002t0003g0022a0002c0002t0003g0144others(10): Show | 15 | HG00140.hp1 HG00280.hp1 HG00733.hp1 others(12): Show |
intron_variant | MODIFIER | c.321+16154dupC | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr13 | 79497677 | |||||
chr13:79497708
|
T | C | 12 | a0003c0003t0005g0010a0003c0003t0005g0030a0003c0003t0005g0031others(9): Show | 13 | HG01981.hp2 HG02451.hp1 HG02486.hp1 others(10): Show |
intron_variant | MODIFIER | c.321+16184T>C | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 1/7 | chr13 | 79497708 | ||||||
chr13:79497790
|
TGG | T | 51 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0012others(48): Show | 57 | HG00140.hp2 HG00323.hp2 HG00408.hp1 others(54): Show |
intron_variant | MODIFIER | c.321+16271_321+1627 others(6): Show |
NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr13 | 79497790 | |||||
chr13:79497790
|
TGGGG | T | 16 | a0001c0001t0001g0088a0001c0001t0004g0003a0001c0001t0004g0009others(13): Show | 22 | HG00099.hp2 HG01069.hp1 HG01071.hp1 others(19): Show |
intron_variant | MODIFIER | c.321+16269_321+1627 others(8): Show |
NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr13 | 79497790 | |||||
chr13:79497791
|
G | GGT | 22 | a0001c0001t0001g0016a0001c0001t0001g0085a0001c0001t0001g0086others(19): Show | 25 | HG00140.hp1 HG00280.hp1 HG00733.hp1 others(22): Show |
intron_variant | MODIFIER | c.321+16268_321+1626 others(6): Show |
NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr13 | 79497791 | |||||
chr13:79497791
|
G | GGTGT | 6 | a0001c0001t0001g0017a0001c0001t0001g0018a0001c0001t0001g0087others(3): Show | 8 | HG01258.hp1 HG01943.hp1 NA18943.hp1 others(5): Show |
intron_variant | MODIFIER | c.321+16268_321+1626 others(8): Show |
NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr13 | 79497791 | |||||
chr13:79497791
|
G | GGTGTGT | 16 | a0001c0001t0001g0011a0001c0001t0001g0019a0001c0001t0001g0045others(13): Show | 18 | HG00544.hp1 HG00735.hp1 HG01891.hp1 others(15): Show |
intron_variant | MODIFIER | c.321+16268_321+1626 others(10): Show |
NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr13 | 79497791 | |||||
chr13:79497791
|
GGGGGGT | G | 6 | a0001c0001t0001g0054a0003c0003t0005g0030a0003c0003t0005g0031others(3): Show | 6 | HG02895.hp2 HG02897.hp2 HG03453.hp1 others(3): Show |
intron_variant | MODIFIER | c.321+16269_321+1627 others(10): Show |
NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr13 | 79497791 | |||||
chr13:79497791
|
GGGGGGTG others(1): Show |
G | 10 | a0001c0001t0004g0134a0001c0001t0004g0136a0001c0001t0019g0135others(7): Show | 11 | HG01981.hp2 HG02451.hp1 HG02486.hp1 others(8): Show |
intron_variant | MODIFIER | c.321+16269_321+1627 others(12): Show |
NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr13 | 79497791 | |||||
chr13:79497791
|
GGGGGGTG others(7): Show |
G | 2 | a0004c0004t0007g0128a0004c0004t0007g0129 | 2 | HG02559.hp1 HG02615.hp2 |
intron_variant | MODIFIER | c.321+16269_321+1628 others(18): Show |
NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr13 | 79497791 | |||||
chr13:79497793
|
G | T | 85 | a0001c0001t0001g0011a0001c0001t0001g0016a0001c0001t0001g0017others(82): Show | 96 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(93): Show |
intron_variant | MODIFIER | c.321+16269G>T | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 1/7 | chr13 | 79497793 | ||||||
chr13:79497795
|
G | T | 139 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0011others(136): Show | 157 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(154): Show |
intron_variant | MODIFIER | c.321+16271G>T | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 1/7 | chr13 | 79497795 | ||||||
chr13:79497797
|
T | G | 4 | a0001c0001t0002g0185a0001c0001t0002g0208a0001c0001t0009g0209others(1): Show | 4 | HG01243.hp1 HG02055.hp2 HG02300.hp2 others(1): Show |
intron_variant | MODIFIER | c.321+16273T>G | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 1/7 | chr13 | 79497797 | ||||||
chr13:79497904
|
C | A | 1 | a0001c0001t0001g0111 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.321+16380C>A | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 1/7 | chr13 | 79497904 | ||||||
chr13:79498029
|
G | T | 1 | a0001c0001t0001g0120 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.321+16505G>T | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 1/7 | chr13 | 79498029 | ||||||
chr13:79498244
|
A | C | 1 | a0001c0001t0003g0225 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.321+16720A>C | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 1/7 | chr13 | 79498244 | ||||||
chr13:79498256
|
G | A | 1 | a0001c0001t0001g0055 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.321+16732G>A | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 1/7 | chr13 | 79498256 | ||||||
chr13:79498262
|
A | G | 1 | a0001c0001t0002g0235 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.321+16738A>G | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 1/7 | chr13 | 79498262 | ||||||
chr13:79498275
|
G | A | 15 | a0003c0003t0005g0010a0003c0003t0005g0029a0003c0003t0005g0030others(12): Show | 16 | HG01981.hp2 HG02451.hp1 HG02486.hp1 others(13): Show |
intron_variant | MODIFIER | c.321+16751G>A | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 1/7 | chr13 | 79498275 | ||||||
chr13:79498325
|
T | G | 2 | a0001c0001t0002g0186a0001c0001t0002g0187 | 2 | NA19062.hp2 NA19075.hp2 |
intron_variant | MODIFIER | c.321+16801T>G | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 1/7 | chr13 | 79498325 | ||||||
chr13:79498336
|
A | G | 2 | a0003c0003t0010g0034a0003c0003t0010g0035 | 2 | HG02965.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.321+16812A>G | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 1/7 | chr13 | 79498336 | ||||||
chr13:79498519
|
A | C | 1 | a0003c0003t0005g0041 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.321+16995A>C | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 1/7 | chr13 | 79498519 | ||||||
chr13:79498595
|
A | C | 1 | a0001c0001t0002g0202 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.321+17071A>C | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 1/7 | chr13 | 79498595 | ||||||
chr13:79498851
|
G | GA | 15 | a0003c0003t0005g0010a0003c0003t0005g0029a0003c0003t0005g0030others(12): Show | 16 | HG01981.hp2 HG02451.hp1 HG02486.hp1 others(13): Show |
intron_variant | MODIFIER | c.321+17333dupA | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr13 | 79498851 | |||||
chr13:79499091
|
A | G | 15 | a0003c0003t0005g0010a0003c0003t0005g0029a0003c0003t0005g0030others(12): Show | 16 | HG01981.hp2 HG02451.hp1 HG02486.hp1 others(13): Show |
intron_variant | MODIFIER | c.321+17567A>G | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 1/7 | chr13 | 79499091 | ||||||
chr13:79499192
|
A | G | 32 | a0001c0001t0003g0006a0001c0001t0003g0158a0001c0001t0003g0159others(29): Show | 37 | HG00140.hp1 HG00280.hp1 HG00733.hp1 others(34): Show |
intron_variant | MODIFIER | c.321+17668A>G | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 1/7 | chr13 | 79499192 | ||||||
chr13:79499382
|
A | G | 6 | a0001c0001t0003g0221a0001c0001t0003g0222a0001c0001t0003g0223others(3): Show | 6 | HG02109.hp1 HG02257.hp1 HG02976.hp2 others(3): Show |
intron_variant | MODIFIER | c.321+17858A>G | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 1/7 | chr13 | 79499382 | ||||||
chr13:79499499
|
CAG | C | 15 | a0003c0003t0005g0010a0003c0003t0005g0029a0003c0003t0005g0030others(12): Show | 16 | HG01981.hp2 HG02451.hp1 HG02486.hp1 others(13): Show |
intron_variant | MODIFIER | c.321+17977_321+1797 others(6): Show |
NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr13 | 79499499 | |||||
chr13:79499668
|
A | G | 3 | a0001c0001t0002g0210a0001c0001t0002g0211a0001c0001t0002g0212 | 3 | NA18969.hp2 NA19006.hp2 NA19063.hp2 |
intron_variant | MODIFIER | c.321+18144A>G | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 1/7 | chr13 | 79499668 | ||||||
chr13:79499670
|
CTG | C | 5 | a0003c0003t0005g0010a0003c0003t0005g0036a0003c0003t0005g0037others(2): Show | 6 | HG01981.hp2 HG02451.hp1 HG02486.hp1 others(3): Show |
intron_variant | MODIFIER | c.321+18149_321+1815 others(6): Show |
NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr13 | 79499670 | |||||
chr13:79500093
|
A | C | 1 | a0001c0001t0001g0071 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.321+18569A>C | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 1/7 | chr13 | 79500093 | ||||||
chr13:79500166
|
C | CA | 13 | a0001c0001t0001g0056a0001c0001t0001g0057a0001c0001t0001g0072others(10): Show | 14 | HG02630.hp1 HG03017.hp1 HG04199.hp2 others(11): Show |
intron_variant | MODIFIER | c.321+18659dupA | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr13 | 79500166 | |||||
chr13:79500166
|
CA | C | 21 | a0001c0001t0001g0069a0001c0001t0001g0070a0001c0001t0001g0111others(18): Show | 22 | HG00738.hp2 HG01192.hp1 HG01261.hp2 others(19): Show |
intron_variant | MODIFIER | c.321+18659delA | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr13 | 79500166 | |||||
chr13:79500447
|
T | G | 2 | a0001c0001t0003g0222a0001c0001t0003g0223 | 2 | HG02109.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.321+18923T>G | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 1/7 | chr13 | 79500447 | ||||||
chr13:79500634
|
G | A | 102 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0011others(99): Show | 114 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(111): Show |
intron_variant | MODIFIER | c.321+19110G>A | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 1/7 | chr13 | 79500634 | ||||||
chr13:79500640
|
C | G | 1 | a0001c0001t0001g0053 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.321+19116C>G | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 1/7 | chr13 | 79500640 | ||||||
chr13:79500646
|
T | C | 172 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0011others(169): Show | 196 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(193): Show |
intron_variant | MODIFIER | c.321+19122T>C | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 1/7 | chr13 | 79500646 | ||||||
chr13:79500815
|
T | C | 21 | a0001c0001t0004g0003a0001c0001t0004g0009a0001c0001t0004g0020others(18): Show | 27 | HG01069.hp1 HG01071.hp1 HG01243.hp2 others(24): Show |
intron_variant | MODIFIER | c.321+19291T>C | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 1/7 | chr13 | 79500815 | ||||||
chr13:79500849
|
C | G | 1 | a0003c0003t0005g0029 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.321+19325C>G | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 1/7 | chr13 | 79500849 | ||||||
chr13:79500988
|
A | G | 5 | a0001c0001t0001g0012a0001c0001t0001g0046a0001c0001t0001g0051others(2): Show | 6 | HG02630.hp2 HG02922.hp1 HG03225.hp1 others(3): Show |
intron_variant | MODIFIER | c.321+19464A>G | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 1/7 | chr13 | 79500988 | ||||||
chr13:79501175
|
G | A | 2 | a0003c0003t0010g0034a0003c0003t0010g0035 | 2 | HG02965.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.322-19635G>A | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 1/7 | chr13 | 79501175 | ||||||
chr13:79501406
|
G | C | 3 | a0001c0001t0004g0134a0001c0001t0004g0136a0001c0001t0019g0135 | 3 | HG02572.hp1 HG02615.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.322-19404G>C | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 1/7 | chr13 | 79501406 | ||||||
chr13:79501426
|
C | T | 2 | a0003c0003t0010g0034a0003c0003t0010g0035 | 2 | HG02965.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.322-19384C>T | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 1/7 | chr13 | 79501426 | ||||||
chr13:79501470
|
G | T | 1 | a0001c0001t0001g0046 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.322-19340G>T | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 1/7 | chr13 | 79501470 | ||||||
chr13:79501633
|
C | T | 1 | a0001c0001t0001g0068 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.322-19177C>T | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 1/7 | chr13 | 79501633 | ||||||
chr13:79501901
|
A | G | 12 | a0003c0003t0005g0010a0003c0003t0005g0030a0003c0003t0005g0031others(9): Show | 13 | HG01981.hp2 HG02451.hp1 HG02486.hp1 others(10): Show |
intron_variant | MODIFIER | c.322-18909A>G | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 1/7 | chr13 | 79501901 | ||||||
chr13:79502250
|
A | T | 1 | a0001c0001t0001g0067 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.322-18560A>T | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 1/7 | chr13 | 79502250 | ||||||
chr13:79502296
|
A | G | 103 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0011others(100): Show | 115 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(112): Show |
intron_variant | MODIFIER | c.322-18514A>G | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 1/7 | chr13 | 79502296 | ||||||
chr13:79502424
|
G | A | 2 | a0005c0005t0002g0155a0005c0005t0002g0157 | 2 | NA18906.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.322-18386G>A | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 1/7 | chr13 | 79502424 | ||||||
chr13:79502463
|
C | T | 1 | a0001c0001t0003g0220 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.322-18347C>T | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 1/7 | chr13 | 79502463 | ||||||
chr13:79502654
|
A | G | 1 | a0001c0001t0001g0066 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.322-18156A>G | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 1/7 | chr13 | 79502654 | ||||||
chr13:79502721
|
G | A | 3 | a0003c0003t0005g0030a0003c0003t0005g0031a0003c0003t0005g0033 | 3 | HG02895.hp2 HG02897.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.322-18089G>A | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 1/7 | chr13 | 79502721 | ||||||
chr13:79502757
|
A | G | 1 | a0001c0001t0001g0096 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.322-18053A>G | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 1/7 | chr13 | 79502757 | ||||||
chr13:79502781
|
A | T | 15 | a0003c0003t0005g0010a0003c0003t0005g0029a0003c0003t0005g0030others(12): Show | 16 | HG01981.hp2 HG02451.hp1 HG02486.hp1 others(13): Show |
intron_variant | MODIFIER | c.322-18029A>T | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 1/7 | chr13 | 79502781 | ||||||
chr13:79502890
|
GT | G | 26 | a0001c0001t0002g0023a0001c0001t0002g0184a0001c0001t0004g0003others(23): Show | 33 | HG01069.hp1 HG01071.hp1 HG01243.hp2 others(30): Show |
intron_variant | MODIFIER | c.322-17908delT | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr13 | 79502890 | |||||
chr13:79503282
|
C | T | 15 | a0003c0003t0005g0010a0003c0003t0005g0029a0003c0003t0005g0030others(12): Show | 16 | HG01981.hp2 HG02451.hp1 HG02486.hp1 others(13): Show |
intron_variant | MODIFIER | c.322-17528C>T | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 1/7 | chr13 | 79503282 | ||||||
chr13:79503314
|
C | T | 5 | a0001c0001t0001g0012a0001c0001t0001g0046a0001c0001t0001g0051others(2): Show | 6 | HG02630.hp2 HG02922.hp1 HG03225.hp1 others(3): Show |
intron_variant | MODIFIER | c.322-17496C>T | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 1/7 | chr13 | 79503314 | ||||||
chr13:79503412
|
G | A | 1 | a0001c0001t0002g0203 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.322-17398G>A | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 1/7 | chr13 | 79503412 | ||||||
chr13:79503434
|
A | G | 1 | a0001c0001t0002g0234 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.322-17376A>G | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 1/7 | chr13 | 79503434 | ||||||
chr13:79503515
|
G | A | 1 | a0001c0001t0002g0190 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.322-17295G>A | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 1/7 | chr13 | 79503515 | ||||||
chr13:79503759
|
T | C | 1 | a0003c0003t0005g0032 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.322-17051T>C | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 1/7 | chr13 | 79503759 | ||||||
chr13:79503788
|
T | C | 1 | a0001c0001t0001g0123 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.322-17022T>C | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 1/7 | chr13 | 79503788 | ||||||
chr13:79503952
|
G | A | 2 | a0001c0001t0002g0186a0001c0001t0002g0187 | 2 | NA19062.hp2 NA19075.hp2 |
intron_variant | MODIFIER | c.322-16858G>A | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 1/7 | chr13 | 79503952 | ||||||
chr13:79503990
|
C | T | 1 | a0001c0001t0012g0177 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.322-16820C>T | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 1/7 | chr13 | 79503990 | ||||||
chr13:79504091
|
A | G | 15 | a0003c0003t0005g0010a0003c0003t0005g0029a0003c0003t0005g0030others(12): Show | 16 | HG01981.hp2 HG02451.hp1 HG02486.hp1 others(13): Show |
intron_variant | MODIFIER | c.322-16719A>G | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 1/7 | chr13 | 79504091 | ||||||
chr13:79504106
|
A | C | 15 | a0003c0003t0005g0010a0003c0003t0005g0029a0003c0003t0005g0030others(12): Show | 16 | HG01981.hp2 HG02451.hp1 HG02486.hp1 others(13): Show |
intron_variant | MODIFIER | c.322-16704A>C | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 1/7 | chr13 | 79504106 | ||||||
chr13:79504114
|
A | G | 2 | a0001c0001t0001g0103a0001c0001t0001g0109 | 2 | NA19054.hp2 NA19065.hp2 |
intron_variant | MODIFIER | c.322-16696A>G | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 1/7 | chr13 | 79504114 | ||||||
chr13:79504136
|
T | C | 1 | a0003c0003t0005g0029 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.322-16674T>C | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 1/7 | chr13 | 79504136 | ||||||
chr13:79504316
|
G | A | 2 | a0001c0001t0001g0028a0001c0001t0001g0242 | 2 | NA18995.hp2 NA19080.hp1 |
intron_variant | MODIFIER | c.322-16494G>A | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 1/7 | chr13 | 79504316 | ||||||
chr13:79504340
|
T | A | 1 | a0001c0001t0002g0178 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.322-16470T>A | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 1/7 | chr13 | 79504340 | ||||||
chr13:79504633
|
AT | A | 158 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0011others(155): Show | 179 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(176): Show |
intron_variant | MODIFIER | c.322-16164delT | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr13 | 79504633 | |||||
chr13:79504647
|
G | A | 25 | a0001c0001t0001g0011a0001c0001t0001g0016a0001c0001t0001g0017others(22): Show | 30 | HG00280.hp2 HG00544.hp1 HG01258.hp1 others(27): Show |
intron_variant | MODIFIER | c.322-16163G>A | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 1/7 | chr13 | 79504647 | ||||||
chr13:79504739
|
T | G | 15 | a0003c0003t0005g0010a0003c0003t0005g0029a0003c0003t0005g0030others(12): Show | 16 | HG01981.hp2 HG02451.hp1 HG02486.hp1 others(13): Show |
intron_variant | MODIFIER | c.322-16071T>G | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 1/7 | chr13 | 79504739 | ||||||
chr13:79505019
|
G | T | 15 | a0003c0003t0005g0010a0003c0003t0005g0029a0003c0003t0005g0030others(12): Show | 16 | HG01981.hp2 HG02451.hp1 HG02486.hp1 others(13): Show |
intron_variant | MODIFIER | c.322-15791G>T | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 1/7 | chr13 | 79505019 | ||||||
chr13:79505220
|
G | C | 15 | a0003c0003t0005g0010a0003c0003t0005g0029a0003c0003t0005g0030others(12): Show | 16 | HG01981.hp2 HG02451.hp1 HG02486.hp1 others(13): Show |
intron_variant | MODIFIER | c.322-15590G>C | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 1/7 | chr13 | 79505220 | ||||||
chr13:79505257
|
A | G | 32 | a0001c0001t0003g0006a0001c0001t0003g0158a0001c0001t0003g0159others(29): Show | 37 | HG00140.hp1 HG00280.hp1 HG00733.hp1 others(34): Show |
intron_variant | MODIFIER | c.322-15553A>G | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 1/7 | chr13 | 79505257 | ||||||
chr13:79505400
|
CAG | C | 12 | a0003c0003t0005g0010a0003c0003t0005g0030a0003c0003t0005g0031others(9): Show | 13 | HG01981.hp2 HG02451.hp1 HG02486.hp1 others(10): Show |
intron_variant | MODIFIER | c.322-15409_322-1540 others(6): Show |
NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 1/7 | chr13 | 79505400 | ||||||
chr13:79505472
|
A | C | 3 | a0001c0001t0001g0108a0001c0001t0001g0122a0001c0001t0001g0126 | 3 | NA18987.hp1 NA19072.hp1 NA19074.hp2 |
intron_variant | MODIFIER | c.322-15338A>C | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 1/7 | chr13 | 79505472 | ||||||
chr13:79505579
|
A | AT | 15 | a0003c0003t0005g0010a0003c0003t0005g0029a0003c0003t0005g0030others(12): Show | 16 | HG01981.hp2 HG02451.hp1 HG02486.hp1 others(13): Show |
intron_variant | MODIFIER | c.322-15231_322-1523 others(5): Show |
NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 1/7 | chr13 | 79505579 | ||||||
chr13:79505601
|
C | G | 1 | a0001c0001t0001g0118 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.322-15209C>G | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 1/7 | chr13 | 79505601 | ||||||
chr13:79505752
|
A | G | 1 | a0001c0001t0001g0097 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.322-15058A>G | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 1/7 | chr13 | 79505752 | ||||||
chr13:79505819
|
T | C | 1 | a0002c0002t0003g0154 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.322-14991T>C | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 1/7 | chr13 | 79505819 | ||||||
chr13:79505836
|
G | T | 1 | a0003c0003t0005g0029 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.322-14974G>T | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 1/7 | chr13 | 79505836 | ||||||
chr13:79505874
|
G | T | 3 | a0001c0001t0002g0169a0001c0001t0002g0170a0001c0001t0002g0230 | 3 | HG00741.hp1 HG03688.hp1 HG03831.hp1 |
intron_variant | MODIFIER | c.322-14936G>T | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 1/7 | chr13 | 79505874 | ||||||
chr13:79505960
|
A | G | 15 | a0003c0003t0005g0010a0003c0003t0005g0029a0003c0003t0005g0030others(12): Show | 16 | HG01981.hp2 HG02451.hp1 HG02486.hp1 others(13): Show |
intron_variant | MODIFIER | c.322-14850A>G | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 1/7 | chr13 | 79505960 | ||||||
chr13:79505966
|
G | A | 1 | a0001c0001t0001g0101 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.322-14844G>A | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 1/7 | chr13 | 79505966 | ||||||
chr13:79505972
|
G | A | 15 | a0003c0003t0005g0010a0003c0003t0005g0029a0003c0003t0005g0030others(12): Show | 16 | HG01981.hp2 HG02451.hp1 HG02486.hp1 others(13): Show |
intron_variant | MODIFIER | c.322-14838G>A | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 1/7 | chr13 | 79505972 | ||||||
chr13:79506472
|
G | A | 3 | a0001c0001t0004g0134a0001c0001t0004g0136a0001c0001t0019g0135 | 3 | HG02572.hp1 HG02615.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.322-14338G>A | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 1/7 | chr13 | 79506472 | ||||||
chr13:79506663
|
A | G | 1 | a0001c0001t0001g0065 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.322-14147A>G | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 1/7 | chr13 | 79506663 | ||||||
chr13:79507179
|
A | G | 15 | a0003c0003t0005g0010a0003c0003t0005g0029a0003c0003t0005g0030others(12): Show | 16 | HG01981.hp2 HG02451.hp1 HG02486.hp1 others(13): Show |
intron_variant | MODIFIER | c.322-13631A>G | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 1/7 | chr13 | 79507179 | ||||||
chr13:79507249
|
G | T | 2 | a0005c0005t0002g0155a0005c0005t0002g0157 | 2 | NA18906.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.322-13561G>T | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 1/7 | chr13 | 79507249 | ||||||
chr13:79507257
|
TTCTGATT others(309): Show |
T | 170 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0011others(167): Show | 194 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(191): Show |
intron_variant | MODIFIER | c.322-13537_322-1322 others(4): Show |
NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr13 | 79507257 | |||||
chr13:79507267
|
G | GT | 11 | a0001c0001t0002g0169a0001c0001t0002g0170a0001c0001t0002g0179others(8): Show | 11 | HG00741.hp1 HG01261.hp1 HG02055.hp2 others(8): Show |
intron_variant | MODIFIER | c.322-13519dupT | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr13 | 79507267 | |||||
chr13:79507626
|
A | G | 12 | a0001c0001t0003g0006a0001c0001t0003g0158a0001c0001t0003g0159others(9): Show | 15 | HG00735.hp2 HG01884.hp2 HG02055.hp1 others(12): Show |
intron_variant | MODIFIER | c.322-13184A>G | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 1/7 | chr13 | 79507626 | ||||||
chr13:79507780
|
G | A | 15 | a0003c0003t0005g0010a0003c0003t0005g0029a0003c0003t0005g0030others(12): Show | 16 | HG01981.hp2 HG02451.hp1 HG02486.hp1 others(13): Show |
intron_variant | MODIFIER | c.322-13030G>A | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 1/7 | chr13 | 79507780 | ||||||
chr13:79507845
|
G | T | 12 | a0003c0003t0005g0010a0003c0003t0005g0030a0003c0003t0005g0031others(9): Show | 13 | HG01981.hp2 HG02451.hp1 HG02486.hp1 others(10): Show |
intron_variant | MODIFIER | c.322-12965G>T | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 1/7 | chr13 | 79507845 | ||||||
chr13:79507882
|
A | C | 2 | a0001c0001t0001g0103a0001c0001t0001g0109 | 2 | NA19054.hp2 NA19065.hp2 |
intron_variant | MODIFIER | c.322-12928A>C | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 1/7 | chr13 | 79507882 | ||||||
chr13:79508379
|
G | A | 2 | a0003c0003t0010g0034a0003c0003t0010g0035 | 2 | HG02965.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.322-12431G>A | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 1/7 | chr13 | 79508379 | ||||||
chr13:79508513
|
T | G | 2 | a0001c0001t0001g0117a0001c0001t0001g0125 | 2 | HG00735.hp1 HG01891.hp1 |
intron_variant | MODIFIER | c.322-12297T>G | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 1/7 | chr13 | 79508513 | ||||||
chr13:79508550
|
A | G | 1 | a0001c0001t0001g0027 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.322-12260A>G | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 1/7 | chr13 | 79508550 | ||||||
chr13:79508619
|
G | A | 15 | a0003c0003t0005g0010a0003c0003t0005g0029a0003c0003t0005g0030others(12): Show | 16 | HG01981.hp2 HG02451.hp1 HG02486.hp1 others(13): Show |
intron_variant | MODIFIER | c.322-12191G>A | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 1/7 | chr13 | 79508619 | ||||||
chr13:79508646
|
C | T | 4 | a0001c0001t0004g0020a0001c0001t0004g0138a0001c0001t0004g0139others(1): Show | 5 | HG01243.hp2 HG03540.hp1 NA18906.hp1 others(2): Show |
intron_variant | MODIFIER | c.322-12164C>T | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 1/7 | chr13 | 79508646 | ||||||
chr13:79508675
|
A | T | 1 | a0003c0003t0005g0029 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.322-12135A>T | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 1/7 | chr13 | 79508675 | ||||||
chr13:79509005
|
T | C | 3 | a0001c0001t0003g0216a0001c0001t0003g0217a0001c0001t0003g0226 | 3 | HG01884.hp2 HG02145.hp2 HG02451.hp2 |
intron_variant | MODIFIER | c.322-11805T>C | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 1/7 | chr13 | 79509005 | ||||||
chr13:79509034
|
A | AT | 12 | a0003c0003t0005g0010a0003c0003t0005g0030a0003c0003t0005g0031others(9): Show | 13 | HG01981.hp2 HG02451.hp1 HG02486.hp1 others(10): Show |
intron_variant | MODIFIER | c.322-11767dupT | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr13 | 79509034 | |||||
chr13:79509064
|
G | A | 14 | a0002c0002t0003g0021a0002c0002t0003g0022a0002c0002t0003g0144others(11): Show | 16 | HG00140.hp1 HG00280.hp1 HG00733.hp1 others(13): Show |
intron_variant | MODIFIER | c.322-11746G>A | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 1/7 | chr13 | 79509064 | ||||||
chr13:79509152
|
G | A | 1 | a0002c0002t0003g0145 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.322-11658G>A | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 1/7 | chr13 | 79509152 | ||||||
chr13:79509179
|
G | A | 12 | a0001c0001t0001g0087a0001c0001t0006g0013a0001c0001t0006g0074others(9): Show | 13 | HG02040.hp2 HG02074.hp1 HG02129.hp2 others(10): Show |
intron_variant | MODIFIER | c.322-11631G>A | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 1/7 | chr13 | 79509179 | ||||||
chr13:79509366
|
A | G | 13 | a0003c0003t0005g0010a0003c0003t0005g0029a0003c0003t0005g0030others(10): Show | 14 | HG01981.hp2 HG02451.hp1 HG02486.hp1 others(11): Show |
intron_variant | MODIFIER | c.322-11444A>G | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 1/7 | chr13 | 79509366 | ||||||
chr13:79509418
|
G | A | 1 | a0002c0002t0003g0146 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.322-11392G>A | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 1/7 | chr13 | 79509418 | ||||||
chr13:79509503
|
T | C | 2 | a0001c0001t0001g0117a0001c0001t0001g0125 | 2 | HG00735.hp1 HG01891.hp1 |
intron_variant | MODIFIER | c.322-11307T>C | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 1/7 | chr13 | 79509503 | ||||||
chr13:79509661
|
A | G | 3 | a0001c0001t0004g0009a0001c0001t0004g0133a0001c0001t0004g0215 | 5 | HG01069.hp1 HG01071.hp1 HG01515.hp1 others(2): Show |
intron_variant | MODIFIER | c.322-11149A>G | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 1/7 | chr13 | 79509661 | ||||||
chr13:79509686
|
T | TAGAGAG | 31 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0015others(28): Show | 36 | HG00140.hp2 HG00323.hp2 HG00408.hp1 others(33): Show |
intron_variant | MODIFIER | c.322-11123_322-1112 others(10): Show |
NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr13 | 79509686 | |||||
chr13:79509688
|
T | G | 33 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0015others(30): Show | 38 | HG00099.hp2 HG00140.hp2 HG00323.hp2 others(35): Show |
intron_variant | MODIFIER | c.322-11122T>G | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 1/7 | chr13 | 79509688 | ||||||
chr13:79509688
|
T | TAGAGAG | 63 | a0001c0001t0001g0011a0001c0001t0001g0016a0001c0001t0001g0017others(60): Show | 69 | HG00280.hp2 HG00544.hp1 HG00735.hp1 others(66): Show |
intron_variant | MODIFIER | c.322-11121_322-1112 others(10): Show |
NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr13 | 79509688 | |||||
chr13:79509688
|
T | TAGAGAGA others(1): Show |
11 | a0001c0001t0003g0006a0001c0001t0003g0161a0001c0001t0003g0216others(8): Show | 15 | HG00735.hp2 HG01069.hp2 HG01175.hp2 others(12): Show |
intron_variant | MODIFIER | c.322-11121_322-1112 others(12): Show |
NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr13 | 79509688 | |||||
chr13:79509690
|
T | G | 115 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0011others(112): Show | 130 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(127): Show |
intron_variant | MODIFIER | c.322-11120T>G | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 1/7 | chr13 | 79509690 | ||||||
chr13:79509690
|
T | TAG | 5 | a0001c0001t0001g0012a0001c0001t0001g0046a0001c0001t0001g0051others(2): Show | 6 | HG02630.hp2 HG02922.hp1 HG03225.hp1 others(3): Show |
intron_variant | MODIFIER | c.322-11104_322-1110 others(6): Show |
NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr13 | 79509690 | |||||
chr13:79509690
|
T | TAGAGAG | 6 | a0001c0001t0001g0082a0001c0001t0001g0086a0001c0001t0001g0100others(3): Show | 6 | HG01978.hp2 HG02280.hp2 HG03041.hp1 others(3): Show |
intron_variant | MODIFIER | c.322-11108_322-1110 others(10): Show |
NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr13 | 79509690 | |||||
chr13:79509690
|
T | TAGAGAGA others(1): Show |
11 | a0001c0001t0003g0159a0001c0001t0003g0227a0002c0002t0003g0021others(8): Show | 12 | HG00733.hp1 HG01167.hp2 HG01168.hp1 others(9): Show |
intron_variant | MODIFIER | c.322-11110_322-1110 others(12): Show |
NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr13 | 79509690 | |||||
chr13:79509690
|
T | TAGAGAGA others(3): Show |
1 | a0001c0001t0001g0083 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.322-11112_322-1110 others(14): Show |
NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr13 | 79509690 | |||||
chr13:79509690
|
T | TATAG | 9 | a0003c0003t0005g0010a0003c0003t0005g0030a0003c0003t0005g0031others(6): Show | 10 | HG01981.hp2 HG02486.hp1 HG02895.hp2 others(7): Show |
intron_variant | MODIFIER | c.322-11119_322-1111 others(8): Show |
NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr13 | 79509690 | |||||
chr13:79509690
|
T | TATAGAGA others(1): Show |
6 | a0001c0001t0003g0158a0002c0002t0003g0145a0002c0002t0003g0150others(3): Show | 6 | HG00140.hp1 HG00280.hp1 HG01361.hp2 others(3): Show |
intron_variant | MODIFIER | c.322-11119_322-1111 others(12): Show |
NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr13 | 79509690 | |||||
chr13:79509692
|
G | T | 21 | a0001c0001t0002g0002a0001c0001t0002g0026a0001c0001t0002g0186others(18): Show | 25 | HG00741.hp2 HG01071.hp2 HG01109.hp2 others(22): Show |
intron_variant | MODIFIER | c.322-11118G>T | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 1/7 | chr13 | 79509692 | ||||||
chr13:79509694
|
G | T | 6 | a0001c0001t0002g0026a0001c0001t0002g0186a0001c0001t0002g0187others(3): Show | 7 | HG02615.hp1 HG02615.hp2 HG03239.hp1 others(4): Show |
intron_variant | MODIFIER | c.322-11116G>T | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 1/7 | chr13 | 79509694 | ||||||
chr13:79509837
|
C | A | 1 | a0001c0001t0002g0172 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.322-10973C>A | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 1/7 | chr13 | 79509837 | ||||||
chr13:79509933
|
T | C | 1 | a0001c0001t0002g0173 | 1 | HG03492.hp1 | intron_variant | MODIFIER | c.322-10877T>C | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 1/7 | chr13 | 79509933 | ||||||
chr13:79510004
|
T | C | 1 | a0001c0001t0001g0088 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.322-10806T>C | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 1/7 | chr13 | 79510004 | ||||||
chr13:79510042
|
A | C | 170 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0011others(167): Show | 194 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(191): Show |
intron_variant | MODIFIER | c.322-10768A>C | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 1/7 | chr13 | 79510042 | ||||||
chr13:79510134
|
C | T | 15 | a0003c0003t0005g0010a0003c0003t0005g0029a0003c0003t0005g0030others(12): Show | 16 | HG01981.hp2 HG02451.hp1 HG02486.hp1 others(13): Show |
intron_variant | MODIFIER | c.322-10676C>T | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 1/7 | chr13 | 79510134 | ||||||
chr13:79510215
|
G | A | 97 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0011others(94): Show | 108 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(105): Show |
intron_variant | MODIFIER | c.322-10595G>A | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 1/7 | chr13 | 79510215 | ||||||
chr13:79510246
|
A | G | 1 | a0003c0003t0005g0029 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.322-10564A>G | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 1/7 | chr13 | 79510246 | ||||||
chr13:79510265
|
C | A | 21 | a0001c0001t0004g0003a0001c0001t0004g0009a0001c0001t0004g0020others(18): Show | 27 | HG01069.hp1 HG01071.hp1 HG01243.hp2 others(24): Show |
intron_variant | MODIFIER | c.322-10545C>A | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 1/7 | chr13 | 79510265 | ||||||
chr13:79510382
|
G | GT | 21 | a0001c0001t0001g0064a0001c0001t0001g0080a0001c0001t0001g0081others(18): Show | 24 | HG00735.hp2 HG01884.hp2 HG02055.hp1 others(21): Show |
intron_variant | MODIFIER | c.322-10415dupT | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr13 | 79510382 | |||||
chr13:79510998
|
C | CA | 39 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0016others(36): Show | 42 | HG00280.hp2 HG00544.hp1 HG00735.hp1 others(39): Show |
intron_variant | MODIFIER | c.322-9794dupA | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr13 | 79510998 | |||||
chr13:79510998
|
C | CAA | 64 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0015others(61): Show | 73 | HG00099.hp2 HG00140.hp2 HG00323.hp2 others(70): Show |
intron_variant | MODIFIER | c.322-9795_322-9794d others(4): Show |
NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr13 | 79510998 | |||||
chr13:79511171
|
T | C | 15 | a0001c0001t0001g0055a0001c0001t0001g0057a0001c0001t0001g0063others(12): Show | 15 | HG01109.hp1 HG01496.hp2 HG01884.hp1 others(12): Show |
intron_variant | MODIFIER | c.322-9639T>C | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 1/7 | chr13 | 79511171 | ||||||
chr13:79511562
|
A | G | 2 | a0003c0003t0010g0034a0003c0003t0010g0035 | 2 | HG02965.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.322-9248A>G | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 1/7 | chr13 | 79511562 | ||||||
chr13:79511712
|
A | T | 12 | a0003c0003t0005g0010a0003c0003t0005g0030a0003c0003t0005g0031others(9): Show | 13 | HG01981.hp2 HG02451.hp1 HG02486.hp1 others(10): Show |
intron_variant | MODIFIER | c.322-9098A>T | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 1/7 | chr13 | 79511712 | ||||||
chr13:79511829
|
G | A | 1 | a0001c0001t0001g0047 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.322-8981G>A | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 1/7 | chr13 | 79511829 | ||||||
chr13:79511936
|
C | A | 1 | a0001c0001t0001g0114 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.322-8874C>A | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 1/7 | chr13 | 79511936 | ||||||
chr13:79512023
|
G | T | 2 | a0005c0005t0002g0155a0005c0005t0002g0157 | 2 | NA18906.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.322-8787G>T | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 1/7 | chr13 | 79512023 | ||||||
chr13:79512316
|
A | G | 3 | a0001c0001t0004g0134a0001c0001t0004g0136a0001c0001t0019g0135 | 3 | HG02572.hp1 HG02615.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.322-8494A>G | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 1/7 | chr13 | 79512316 | ||||||
chr13:79512376
|
T | G | 5 | a0001c0001t0001g0012a0001c0001t0001g0046a0001c0001t0001g0051others(2): Show | 6 | HG02630.hp2 HG02922.hp1 HG03225.hp1 others(3): Show |
intron_variant | MODIFIER | c.322-8434T>G | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 1/7 | chr13 | 79512376 | ||||||
chr13:79512459
|
A | G | 4 | a0001c0001t0001g0063a0001c0001t0001g0079a0001c0001t0001g0114others(1): Show | 4 | HG01109.hp1 HG01496.hp2 HG02109.hp2 others(1): Show |
intron_variant | MODIFIER | c.322-8351A>G | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 1/7 | chr13 | 79512459 | ||||||
chr13:79513047
|
C | T | 1 | a0001c0001t0003g0219 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.322-7763C>T | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 1/7 | chr13 | 79513047 | ||||||
chr13:79513141
|
T | A | 15 | a0003c0003t0005g0010a0003c0003t0005g0029a0003c0003t0005g0030others(12): Show | 16 | HG01981.hp2 HG02451.hp1 HG02486.hp1 others(13): Show |
intron_variant | MODIFIER | c.322-7669T>A | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 1/7 | chr13 | 79513141 | ||||||
chr13:79513281
|
A | T | 2 | a0001c0001t0001g0117a0001c0001t0001g0125 | 2 | HG00735.hp1 HG01891.hp1 |
intron_variant | MODIFIER | c.322-7529A>T | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 1/7 | chr13 | 79513281 | ||||||
chr13:79513512
|
T | C | 6 | a0001c0001t0003g0221a0001c0001t0003g0222a0001c0001t0003g0223others(3): Show | 6 | HG02109.hp1 HG02257.hp1 HG02976.hp2 others(3): Show |
intron_variant | MODIFIER | c.322-7298T>C | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 1/7 | chr13 | 79513512 | ||||||
chr13:79513686
|
C | G | 1 | a0001c0001t0001g0126 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.322-7124C>G | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 1/7 | chr13 | 79513686 | ||||||
chr13:79513688
|
T | C | 12 | a0003c0003t0005g0010a0003c0003t0005g0030a0003c0003t0005g0031others(9): Show | 13 | HG01981.hp2 HG02451.hp1 HG02486.hp1 others(10): Show |
intron_variant | MODIFIER | c.322-7122T>C | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 1/7 | chr13 | 79513688 | ||||||
chr13:79513715
|
CT | C | 41 | a0001c0001t0001g0011a0001c0001t0001g0016a0001c0001t0001g0017others(38): Show | 48 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(45): Show |
intron_variant | MODIFIER | c.322-7083delT | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr13 | 79513715 | |||||
chr13:79513802
|
T | A | 2 | a0003c0003t0010g0034a0003c0003t0010g0035 | 2 | HG02965.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.322-7008T>A | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 1/7 | chr13 | 79513802 | ||||||
chr13:79513849
|
A | G | 1 | a0001c0001t0001g0057 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.322-6961A>G | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 1/7 | chr13 | 79513849 | ||||||
chr13:79513930
|
C | G | 15 | a0003c0003t0005g0010a0003c0003t0005g0029a0003c0003t0005g0030others(12): Show | 16 | HG01981.hp2 HG02451.hp1 HG02486.hp1 others(13): Show |
intron_variant | MODIFIER | c.322-6880C>G | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 1/7 | chr13 | 79513930 | ||||||
chr13:79513972
|
G | A | 2 | a0001c0001t0001g0017a0001c0001t0001g0018 | 4 | NA18944.hp2 NA18969.hp1 NA19055.hp1 others(1): Show |
intron_variant | MODIFIER | c.322-6838G>A | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 1/7 | chr13 | 79513972 | ||||||
chr13:79514186
|
C | T | 2 | a0003c0003t0010g0034a0003c0003t0010g0035 | 2 | HG02965.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.322-6624C>T | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 1/7 | chr13 | 79514186 | ||||||
chr13:79514469
|
A | T | 1 | a0001c0001t0002g0213 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.322-6341A>T | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 1/7 | chr13 | 79514469 | ||||||
chr13:79514504
|
A | ATC | 21 | a0001c0001t0004g0003a0001c0001t0004g0009a0001c0001t0004g0020others(18): Show | 27 | HG01069.hp1 HG01071.hp1 HG01243.hp2 others(24): Show |
intron_variant | MODIFIER | c.322-6306_322-6305i others(4): Show |
NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 1/7 | chr13 | 79514504 | ||||||
chr13:79514505
|
A | C | 21 | a0001c0001t0004g0003a0001c0001t0004g0009a0001c0001t0004g0020others(18): Show | 27 | HG01069.hp1 HG01071.hp1 HG01243.hp2 others(24): Show |
intron_variant | MODIFIER | c.322-6305A>C | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 1/7 | chr13 | 79514505 | ||||||
chr13:79514548
|
A | G | 21 | a0001c0001t0004g0003a0001c0001t0004g0009a0001c0001t0004g0020others(18): Show | 27 | HG01069.hp1 HG01071.hp1 HG01243.hp2 others(24): Show |
intron_variant | MODIFIER | c.322-6262A>G | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 1/7 | chr13 | 79514548 | ||||||
chr13:79514550
|
A | T | 1 | a0002c0002t0003g0160 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.322-6260A>T | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 1/7 | chr13 | 79514550 | ||||||
chr13:79514593
|
C | T | 2 | a0001c0001t0001g0087a0001c0001t0017g0094 | 2 | NA18943.hp1 NA18979.hp2 |
intron_variant | MODIFIER | c.322-6217C>T | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 1/7 | chr13 | 79514593 | ||||||
chr13:79514677
|
T | C | 1 | a0001c0001t0013g0167 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.322-6133T>C | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 1/7 | chr13 | 79514677 | ||||||
chr13:79514787
|
G | A | 92 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0011others(89): Show | 100 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(97): Show |
intron_variant | MODIFIER | c.322-6023G>A | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 1/7 | chr13 | 79514787 | ||||||
chr13:79514942
|
G | A | 12 | a0003c0003t0005g0010a0003c0003t0005g0030a0003c0003t0005g0031others(9): Show | 13 | HG01981.hp2 HG02451.hp1 HG02486.hp1 others(10): Show |
intron_variant | MODIFIER | c.322-5868G>A | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 1/7 | chr13 | 79514942 | ||||||
chr13:79514964
|
T | C | 1 | a0001c0001t0001g0086 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.322-5846T>C | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 1/7 | chr13 | 79514964 | ||||||
chr13:79515003
|
G | C | 8 | a0003c0003t0005g0010a0003c0003t0005g0036a0003c0003t0005g0037others(5): Show | 9 | HG01981.hp2 HG02451.hp1 HG02486.hp1 others(6): Show |
intron_variant | MODIFIER | c.322-5807G>C | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 1/7 | chr13 | 79515003 | ||||||
chr13:79515135
|
A | C | 1 | a0003c0003t0010g0034 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.322-5675A>C | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 1/7 | chr13 | 79515135 | ||||||
chr13:79515208
|
A | AATCTTAT others(14): Show |
18 | a0001c0001t0004g0003a0001c0001t0004g0009a0001c0001t0004g0020others(15): Show | 24 | HG01069.hp1 HG01071.hp1 HG01243.hp2 others(21): Show |
intron_variant | MODIFIER | c.322-5601_322-5600i others(23): Show |
NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr13 | 79515208 | |||||
chr13:79515211
|
G | A | 18 | a0001c0001t0004g0003a0001c0001t0004g0009a0001c0001t0004g0020others(15): Show | 24 | HG01069.hp1 HG01071.hp1 HG01243.hp2 others(21): Show |
intron_variant | MODIFIER | c.322-5599G>A | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 1/7 | chr13 | 79515211 | ||||||
chr13:79515213
|
T | A | 18 | a0001c0001t0004g0003a0001c0001t0004g0009a0001c0001t0004g0020others(15): Show | 24 | HG01069.hp1 HG01071.hp1 HG01243.hp2 others(21): Show |
intron_variant | MODIFIER | c.322-5597T>A | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 1/7 | chr13 | 79515213 | ||||||
chr13:79515214
|
T | A | 18 | a0001c0001t0004g0003a0001c0001t0004g0009a0001c0001t0004g0020others(15): Show | 24 | HG01069.hp1 HG01071.hp1 HG01243.hp2 others(21): Show |
intron_variant | MODIFIER | c.322-5596T>A | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 1/7 | chr13 | 79515214 | ||||||
chr13:79515813
|
T | C | 6 | a0001c0001t0003g0158a0001c0001t0003g0159a0001c0001t0003g0217others(3): Show | 6 | HG00735.hp2 HG01884.hp2 HG02451.hp2 others(3): Show |
intron_variant | MODIFIER | c.322-4997T>C | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 1/7 | chr13 | 79515813 | ||||||
chr13:79515858
|
G | GT | 91 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0011others(88): Show | 103 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(100): Show |
intron_variant | MODIFIER | c.322-4942dupT | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr13 | 79515858 | |||||
chr13:79515858
|
GT | G | 15 | a0003c0003t0005g0010a0003c0003t0005g0029a0003c0003t0005g0030others(12): Show | 16 | HG01981.hp2 HG02451.hp1 HG02486.hp1 others(13): Show |
intron_variant | MODIFIER | c.322-4942delT | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr13 | 79515858 | |||||
chr13:79515868
|
T | TC | 12 | a0001c0001t0001g0055a0001c0001t0001g0057a0001c0001t0001g0063others(9): Show | 12 | HG01109.hp1 HG01496.hp2 HG01884.hp1 others(9): Show |
intron_variant | MODIFIER | c.322-4938dupC | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr13 | 79515868 | |||||
chr13:79515902
|
A | G | 1 | a0001c0001t0001g0051 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.322-4908A>G | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 1/7 | chr13 | 79515902 | ||||||
chr13:79515910
|
C | T | 1 | a0001c0001t0003g0218 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.322-4900C>T | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 1/7 | chr13 | 79515910 | ||||||
chr13:79515941
|
G | C | 15 | a0003c0003t0005g0010a0003c0003t0005g0029a0003c0003t0005g0030others(12): Show | 16 | HG01981.hp2 HG02451.hp1 HG02486.hp1 others(13): Show |
intron_variant | MODIFIER | c.322-4869G>C | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 1/7 | chr13 | 79515941 | ||||||
chr13:79515979
|
C | T | 29 | a0001c0001t0002g0004a0001c0001t0002g0005a0001c0001t0002g0024others(26): Show | 36 | HG00099.hp1 HG00323.hp1 HG00408.hp2 others(33): Show |
intron_variant | MODIFIER | c.322-4831C>T | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 1/7 | chr13 | 79515979 | ||||||
chr13:79516024
|
G | A | 25 | a0001c0001t0001g0011a0001c0001t0001g0016a0001c0001t0001g0017others(22): Show | 30 | HG00280.hp2 HG00544.hp1 HG01258.hp1 others(27): Show |
intron_variant | MODIFIER | c.322-4786G>A | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 1/7 | chr13 | 79516024 | ||||||
chr13:79516028
|
T | C | 2 | a0003c0003t0010g0034a0003c0003t0010g0035 | 2 | HG02965.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.322-4782T>C | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 1/7 | chr13 | 79516028 | ||||||
chr13:79516244
|
T | TTTTTG | 15 | a0003c0003t0005g0010a0003c0003t0005g0029a0003c0003t0005g0030others(12): Show | 16 | HG01981.hp2 HG02451.hp1 HG02486.hp1 others(13): Show |
intron_variant | MODIFIER | c.322-4546_322-4542d others(7): Show |
NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr13 | 79516244 | |||||
chr13:79516311
|
C | T | 1 | a0001c0001t0002g0197 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.322-4499C>T | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 1/7 | chr13 | 79516311 | ||||||
chr13:79516452
|
G | A | 4 | a0001c0001t0003g0006a0001c0001t0003g0161a0001c0001t0003g0227others(1): Show | 7 | HG02257.hp2 HG02572.hp2 HG02922.hp2 others(4): Show |
intron_variant | MODIFIER | c.322-4358G>A | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 1/7 | chr13 | 79516452 | ||||||
chr13:79516480
|
C | T | 14 | a0002c0002t0003g0021a0002c0002t0003g0022a0002c0002t0003g0144others(11): Show | 16 | HG00140.hp1 HG00280.hp1 HG00733.hp1 others(13): Show |
intron_variant | MODIFIER | c.322-4330C>T | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 1/7 | chr13 | 79516480 | ||||||
chr13:79516593
|
T | C | 1 | a0001c0001t0002g0179 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.322-4217T>C | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 1/7 | chr13 | 79516593 | ||||||
chr13:79516622
|
T | A | 1 | a0001c0001t0002g0186 | 1 | NA19075.hp2 | intron_variant | MODIFIER | c.322-4188T>A | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 1/7 | chr13 | 79516622 | ||||||
chr13:79516730
|
A | G | 170 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0011others(167): Show | 194 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(191): Show |
intron_variant | MODIFIER | c.322-4080A>G | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 1/7 | chr13 | 79516730 | ||||||
chr13:79516748
|
T | C | 1 | a0003c0003t0005g0032 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.322-4062T>C | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 1/7 | chr13 | 79516748 | ||||||
chr13:79516767
|
T | A | 1 | a0001c0001t0002g0185 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.322-4043T>A | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 1/7 | chr13 | 79516767 | ||||||
chr13:79517288
|
G | A | 2 | a0003c0003t0010g0034a0003c0003t0010g0035 | 2 | HG02965.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.322-3522G>A | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 1/7 | chr13 | 79517288 | ||||||
chr13:79517404
|
A | G | 170 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0011others(167): Show | 194 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(191): Show |
intron_variant | MODIFIER | c.322-3406A>G | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 1/7 | chr13 | 79517404 | ||||||
chr13:79517408
|
T | C | 56 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0015others(53): Show | 62 | HG00099.hp2 HG00140.hp2 HG00323.hp2 others(59): Show |
intron_variant | MODIFIER | c.322-3402T>C | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 1/7 | chr13 | 79517408 | ||||||
chr13:79517408
|
T | TTACTCTC others(16): Show |
3 | a0001c0001t0004g0134a0001c0001t0004g0136a0001c0001t0019g0135 | 3 | HG02572.hp1 HG02615.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.322-3400_322-3399i others(25): Show |
NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr13 | 79517408 | |||||
chr13:79517411
|
T | C | 3 | a0001c0001t0004g0134a0001c0001t0004g0136a0001c0001t0019g0135 | 3 | HG02572.hp1 HG02615.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.322-3399T>C | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 1/7 | chr13 | 79517411 | ||||||
chr13:79517646
|
A | G | 103 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0011others(100): Show | 115 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(112): Show |
intron_variant | MODIFIER | c.322-3164A>G | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 1/7 | chr13 | 79517646 | ||||||
chr13:79517724
|
T | C | 21 | a0001c0001t0004g0003a0001c0001t0004g0009a0001c0001t0004g0020others(18): Show | 27 | HG01069.hp1 HG01071.hp1 HG01243.hp2 others(24): Show |
intron_variant | MODIFIER | c.322-3086T>C | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 1/7 | chr13 | 79517724 | ||||||
chr13:79517883
|
G | C | 18 | a0001c0001t0004g0003a0001c0001t0004g0009a0001c0001t0004g0020others(15): Show | 24 | HG01069.hp1 HG01071.hp1 HG01243.hp2 others(21): Show |
intron_variant | MODIFIER | c.322-2927G>C | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 1/7 | chr13 | 79517883 | ||||||
chr13:79518032
|
A | AC | 172 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0011others(169): Show | 196 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(193): Show |
intron_variant | MODIFIER | c.322-2778_322-2777i others(3): Show |
NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 1/7 | chr13 | 79518032 | ||||||
chr13:79518120
|
G | A | 21 | a0001c0001t0004g0003a0001c0001t0004g0009a0001c0001t0004g0020others(18): Show | 27 | HG01069.hp1 HG01071.hp1 HG01243.hp2 others(24): Show |
intron_variant | MODIFIER | c.322-2690G>A | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 1/7 | chr13 | 79518120 | ||||||
chr13:79518148
|
C | T | 3 | a0003c0003t0005g0030a0003c0003t0005g0031a0003c0003t0005g0033 | 3 | HG02895.hp2 HG02897.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.322-2662C>T | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 1/7 | chr13 | 79518148 | ||||||
chr13:79518149
|
G | A | 1 | a0001c0001t0003g0221 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.322-2661G>A | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 1/7 | chr13 | 79518149 | ||||||
chr13:79518787
|
A | C | 6 | a0001c0001t0003g0221a0001c0001t0003g0222a0001c0001t0003g0223others(3): Show | 6 | HG02109.hp1 HG02257.hp1 HG02976.hp2 others(3): Show |
intron_variant | MODIFIER | c.322-2023A>C | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 1/7 | chr13 | 79518787 | ||||||
chr13:79519353
|
A | G | 21 | a0001c0001t0004g0003a0001c0001t0004g0009a0001c0001t0004g0020others(18): Show | 27 | HG01069.hp1 HG01071.hp1 HG01243.hp2 others(24): Show |
intron_variant | MODIFIER | c.322-1457A>G | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 1/7 | chr13 | 79519353 | ||||||
chr13:79519370
|
A | G | 1 | a0001c0001t0001g0018 | 2 | NA18944.hp2 NA19055.hp1 |
intron_variant | MODIFIER | c.322-1440A>G | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 1/7 | chr13 | 79519370 | ||||||
chr13:79519543
|
T | A | 5 | a0001c0001t0001g0012a0001c0001t0001g0046a0001c0001t0001g0051others(2): Show | 6 | HG02630.hp2 HG02922.hp1 HG03225.hp1 others(3): Show |
intron_variant | MODIFIER | c.322-1267T>A | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 1/7 | chr13 | 79519543 | ||||||
chr13:79519656
|
G | A | 13 | a0003c0003t0005g0010a0003c0003t0005g0029a0003c0003t0005g0030others(10): Show | 14 | HG01981.hp2 HG02451.hp1 HG02486.hp1 others(11): Show |
intron_variant | MODIFIER | c.322-1154G>A | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 1/7 | chr13 | 79519656 | ||||||
chr13:79519690
|
T | G | 172 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0011others(169): Show | 196 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(193): Show |
intron_variant | MODIFIER | c.322-1120T>G | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 1/7 | chr13 | 79519690 | ||||||
chr13:79519756
|
A | G | 1 | a0001c0001t0002g0232 | 1 | NA19080.hp2 | intron_variant | MODIFIER | c.322-1054A>G | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 1/7 | chr13 | 79519756 | ||||||
chr13:79519764
|
A | G | 12 | a0001c0001t0003g0006a0001c0001t0003g0158a0001c0001t0003g0159others(9): Show | 15 | HG00735.hp2 HG01884.hp2 HG02055.hp1 others(12): Show |
intron_variant | MODIFIER | c.322-1046A>G | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 1/7 | chr13 | 79519764 | ||||||
chr13:79519998
|
AC | A | 14 | a0002c0002t0003g0021a0002c0002t0003g0022a0002c0002t0003g0144others(11): Show | 16 | HG00140.hp1 HG00280.hp1 HG00733.hp1 others(13): Show |
intron_variant | MODIFIER | c.322-810delC | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr13 | 79519998 | |||||
chr13:79520108
|
A | G | 1 | a0001c0001t0001g0162 | 1 | HG01517.hp2 | intron_variant | MODIFIER | c.322-702A>G | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 1/7 | chr13 | 79520108 | ||||||
chr13:79520359
|
G | T | 1 | a0001c0001t0006g0076 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.322-451G>T | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 1/7 | chr13 | 79520359 | ||||||
chr13:79520711
|
G | C | 12 | a0003c0003t0005g0010a0003c0003t0005g0030a0003c0003t0005g0031others(9): Show | 13 | HG01981.hp2 HG02451.hp1 HG02486.hp1 others(10): Show |
intron_variant | MODIFIER | c.322-99G>C | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 1/7 | chr13 | 79520711 | ||||||
chr13:79521008
|
C | CT | 15 | a0003c0003t0005g0010a0003c0003t0005g0029a0003c0003t0005g0030others(12): Show | 16 | HG01981.hp2 HG02451.hp1 HG02486.hp1 others(13): Show |
intron_variant | MODIFIER | c.487+45dupT | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr13 | 79521008 | |||||
chr13:79521008
|
C | CTT | 20 | a0001c0001t0004g0003a0001c0001t0004g0009a0001c0001t0004g0020others(17): Show | 26 | HG01069.hp1 HG01071.hp1 HG01243.hp2 others(23): Show |
intron_variant | MODIFIER | c.487+44_487+45dupTT | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr13 | 79521008 | |||||
chr13:79521022
|
A | T | 21 | a0001c0001t0004g0003a0001c0001t0004g0009a0001c0001t0004g0020others(18): Show | 27 | HG01069.hp1 HG01071.hp1 HG01243.hp2 others(24): Show |
intron_variant | MODIFIER | c.487+47A>T | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 2/7 | chr13 | 79521022 | ||||||
chr13:79521313
|
C | T | 2 | a0001c0001t0004g0020a0001c0001t0004g0140 | 3 | HG01243.hp2 HG03540.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.487+338C>T | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 2/7 | chr13 | 79521313 | ||||||
chr13:79521406
|
C | T | 102 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0011others(99): Show | 114 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(111): Show |
intron_variant | MODIFIER | c.487+431C>T | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 2/7 | chr13 | 79521406 | ||||||
chr13:79521791
|
A | G | 32 | a0001c0001t0003g0006a0001c0001t0003g0158a0001c0001t0003g0159others(29): Show | 37 | HG00140.hp1 HG00280.hp1 HG00733.hp1 others(34): Show |
intron_variant | MODIFIER | c.487+816A>G | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 2/7 | chr13 | 79521791 | ||||||
chr13:79521821
|
T | G | 3 | a0001c0001t0002g0023a0001c0001t0002g0184a0001c0001t0002g0211 | 4 | NA18982.hp2 NA19060.hp1 NA19063.hp1 others(1): Show |
intron_variant | MODIFIER | c.487+846T>G | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 2/7 | chr13 | 79521821 | ||||||
chr13:79521822
|
G | T | 1 | a0002c0002t0003g0149 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.487+847G>T | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 2/7 | chr13 | 79521822 | ||||||
chr13:79521823
|
C | CT | 26 | a0001c0001t0001g0118a0001c0001t0002g0002a0001c0001t0002g0174others(23): Show | 31 | HG00140.hp1 HG00280.hp1 HG00733.hp1 others(28): Show |
intron_variant | MODIFIER | c.487+865dupT | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr13 | 79521823 | |||||
chr13:79521823
|
C | T | 1 | a0002c0002t0003g0149 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.487+848C>T | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 2/7 | chr13 | 79521823 | ||||||
chr13:79521976
|
G | C | 170 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0011others(167): Show | 194 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(191): Show |
intron_variant | MODIFIER | c.487+1001G>C | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 2/7 | chr13 | 79521976 | ||||||
chr13:79522166
|
A | G | 2 | a0004c0004t0007g0127a0004c0004t0007g0141 | 2 | HG01952.hp1 HG02145.hp1 |
intron_variant | MODIFIER | c.487+1191A>G | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 2/7 | chr13 | 79522166 | ||||||
chr13:79522262
|
A | C | 1 | a0001c0001t0003g0219 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.487+1287A>C | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 2/7 | chr13 | 79522262 | ||||||
chr13:79522810
|
G | A | 21 | a0001c0001t0004g0003a0001c0001t0004g0009a0001c0001t0004g0020others(18): Show | 27 | HG01069.hp1 HG01071.hp1 HG01243.hp2 others(24): Show |
intron_variant | MODIFIER | c.487+1835G>A | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 2/7 | chr13 | 79522810 | ||||||
chr13:79522862
|
G | A | 1 | a0001c0001t0001g0048 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.487+1887G>A | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 2/7 | chr13 | 79522862 | ||||||
chr13:79522880
|
A | G | 1 | a0001c0001t0006g0075 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.487+1905A>G | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 2/7 | chr13 | 79522880 | ||||||
chr13:79523021
|
A | G | 21 | a0001c0001t0004g0003a0001c0001t0004g0009a0001c0001t0004g0020others(18): Show | 27 | HG01069.hp1 HG01071.hp1 HG01243.hp2 others(24): Show |
intron_variant | MODIFIER | c.487+2046A>G | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 2/7 | chr13 | 79523021 | ||||||
chr13:79523132
|
C | T | 36 | a0001c0001t0004g0003a0001c0001t0004g0009a0001c0001t0004g0020others(33): Show | 43 | HG01069.hp1 HG01071.hp1 HG01243.hp2 others(40): Show |
intron_variant | MODIFIER | c.487+2157C>T | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 2/7 | chr13 | 79523132 | ||||||
chr13:79523136
|
A | G | 1 | a0001c0001t0001g0048 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.487+2161A>G | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 2/7 | chr13 | 79523136 | ||||||
chr13:79523159
|
A | G | 6 | a0001c0001t0003g0221a0001c0001t0003g0222a0001c0001t0003g0223others(3): Show | 6 | HG02109.hp1 HG02257.hp1 HG02976.hp2 others(3): Show |
intron_variant | MODIFIER | c.487+2184A>G | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 2/7 | chr13 | 79523159 | ||||||
chr13:79523262
|
C | T | 1 | a0005c0005t0002g0155 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.487+2287C>T | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 2/7 | chr13 | 79523262 | ||||||
chr13:79523282
|
G | T | 14 | a0002c0002t0003g0021a0002c0002t0003g0022a0002c0002t0003g0144others(11): Show | 16 | HG00140.hp1 HG00280.hp1 HG00733.hp1 others(13): Show |
intron_variant | MODIFIER | c.487+2307G>T | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 2/7 | chr13 | 79523282 | ||||||
chr13:79523485
|
G | T | 1 | a0001c0001t0002g0229 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.487+2510G>T | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 2/7 | chr13 | 79523485 | ||||||
chr13:79523567
|
C | T | 15 | a0003c0003t0005g0010a0003c0003t0005g0029a0003c0003t0005g0030others(12): Show | 16 | HG01981.hp2 HG02451.hp1 HG02486.hp1 others(13): Show |
intron_variant | MODIFIER | c.487+2592C>T | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 2/7 | chr13 | 79523567 | ||||||
chr13:79523574
|
T | G | 2 | a0003c0003t0010g0034a0003c0003t0010g0035 | 2 | HG02965.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.487+2599T>G | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 2/7 | chr13 | 79523574 | ||||||
chr13:79523580
|
C | G | 71 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0015others(68): Show | 77 | HG00099.hp2 HG00140.hp2 HG00323.hp2 others(74): Show |
intron_variant | MODIFIER | c.487+2605C>G | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 2/7 | chr13 | 79523580 | ||||||
chr13:79523701
|
T | A | 4 | a0004c0004t0007g0127a0004c0004t0007g0128a0004c0004t0007g0129others(1): Show | 4 | HG01952.hp1 HG02145.hp1 HG02559.hp1 others(1): Show |
intron_variant | MODIFIER | c.487+2726T>A | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 2/7 | chr13 | 79523701 | ||||||
chr13:79523726
|
G | A | 14 | a0002c0002t0003g0021a0002c0002t0003g0022a0002c0002t0003g0144others(11): Show | 16 | HG00140.hp1 HG00280.hp1 HG00733.hp1 others(13): Show |
intron_variant | MODIFIER | c.487+2751G>A | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 2/7 | chr13 | 79523726 | ||||||
chr13:79523833
|
G | T | 1 | a0001c0001t0003g0221 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.487+2858G>T | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 2/7 | chr13 | 79523833 | ||||||
chr13:79523869
|
C | G | 3 | a0001c0001t0004g0134a0001c0001t0004g0136a0001c0001t0019g0135 | 3 | HG02572.hp1 HG02615.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.487+2894C>G | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 2/7 | chr13 | 79523869 | ||||||
chr13:79523903
|
T | G | 21 | a0001c0001t0004g0003a0001c0001t0004g0009a0001c0001t0004g0020others(18): Show | 27 | HG01069.hp1 HG01071.hp1 HG01243.hp2 others(24): Show |
intron_variant | MODIFIER | c.487+2928T>G | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 2/7 | chr13 | 79523903 | ||||||
chr13:79524039
|
T | G | 18 | a0001c0001t0004g0003a0001c0001t0004g0009a0001c0001t0004g0020others(15): Show | 24 | HG01069.hp1 HG01071.hp1 HG01243.hp2 others(21): Show |
intron_variant | MODIFIER | c.487+3064T>G | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 2/7 | chr13 | 79524039 | ||||||
chr13:79524047
|
T | C | 1 | a0001c0001t0002g0175 | 1 | NA18943.hp2 | intron_variant | MODIFIER | c.487+3072T>C | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 2/7 | chr13 | 79524047 | ||||||
chr13:79524057
|
G | A | 21 | a0001c0001t0004g0003a0001c0001t0004g0009a0001c0001t0004g0020others(18): Show | 27 | HG01069.hp1 HG01071.hp1 HG01243.hp2 others(24): Show |
intron_variant | MODIFIER | c.487+3082G>A | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 2/7 | chr13 | 79524057 | ||||||
chr13:79524108
|
C | A | 14 | a0002c0002t0003g0021a0002c0002t0003g0022a0002c0002t0003g0144others(11): Show | 16 | HG00140.hp1 HG00280.hp1 HG00733.hp1 others(13): Show |
intron_variant | MODIFIER | c.487+3133C>A | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 2/7 | chr13 | 79524108 | ||||||
chr13:79524133
|
C | G | 1 | a0001c0006t0006g0084 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.487+3158C>G | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 2/7 | chr13 | 79524133 | ||||||
chr13:79524188
|
G | A | 3 | a0001c0001t0001g0108a0001c0001t0001g0122a0001c0001t0001g0126 | 3 | NA18987.hp1 NA19072.hp1 NA19074.hp2 |
intron_variant | MODIFIER | c.487+3213G>A | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 2/7 | chr13 | 79524188 | ||||||
chr13:79524526
|
A | C | 3 | a0001c0001t0004g0134a0001c0001t0004g0136a0001c0001t0019g0135 | 3 | HG02572.hp1 HG02615.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.487+3551A>C | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 2/7 | chr13 | 79524526 | ||||||
chr13:79524854
|
C | A | 102 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0011others(99): Show | 114 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(111): Show |
intron_variant | MODIFIER | c.487+3879C>A | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 2/7 | chr13 | 79524854 | ||||||
chr13:79524983
|
G | A | 72 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0004others(69): Show | 89 | HG00099.hp1 HG00323.hp1 HG00408.hp2 others(86): Show |
intron_variant | MODIFIER | c.487+4008G>A | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 2/7 | chr13 | 79524983 | ||||||
chr13:79525217
|
C | T | 1 | a0001c0001t0001g0108 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.487+4242C>T | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 2/7 | chr13 | 79525217 | ||||||
chr13:79525338
|
G | A | 142 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0004others(139): Show | 171 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(168): Show |
intron_variant | MODIFIER | c.487+4363G>A | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 2/7 | chr13 | 79525338 | ||||||
chr13:79525396
|
T | G | 1 | a0002c0002t0003g0150 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.487+4421T>G | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 2/7 | chr13 | 79525396 | ||||||
chr13:79525542
|
A | G | 15 | a0001c0001t0001g0055a0001c0001t0001g0057a0001c0001t0001g0063others(12): Show | 15 | HG01109.hp1 HG01496.hp2 HG01884.hp1 others(12): Show |
intron_variant | MODIFIER | c.487+4567A>G | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 2/7 | chr13 | 79525542 | ||||||
chr13:79525771
|
T | C | 1 | a0003c0003t0005g0029 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.487+4796T>C | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 2/7 | chr13 | 79525771 | ||||||
chr13:79525833
|
C | A | 1 | a0003c0003t0005g0029 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.487+4858C>A | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 2/7 | chr13 | 79525833 | ||||||
chr13:79525958
|
G | A | 15 | a0003c0003t0005g0010a0003c0003t0005g0029a0003c0003t0005g0030others(12): Show | 16 | HG01981.hp2 HG02451.hp1 HG02486.hp1 others(13): Show |
intron_variant | MODIFIER | c.487+4983G>A | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 2/7 | chr13 | 79525958 | ||||||
chr13:79526092
|
A | G | 5 | a0001c0001t0001g0012a0001c0001t0001g0046a0001c0001t0001g0051others(2): Show | 6 | HG02630.hp2 HG02922.hp1 HG03225.hp1 others(3): Show |
intron_variant | MODIFIER | c.487+5117A>G | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 2/7 | chr13 | 79526092 | ||||||
chr13:79526186
|
G | T | 10 | a0001c0001t0002g0005a0001c0001t0002g0024a0001c0001t0002g0171others(7): Show | 14 | HG00408.hp2 HG02071.hp1 HG02129.hp1 others(11): Show |
intron_variant | MODIFIER | c.487+5211G>T | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 2/7 | chr13 | 79526186 | ||||||
chr13:79526677
|
G | A | 1 | a0001c0001t0001g0069 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.487+5702G>A | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 2/7 | chr13 | 79526677 | ||||||
chr13:79526723
|
A | C | 1 | a0001c0001t0002g0183 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.487+5748A>C | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 2/7 | chr13 | 79526723 | ||||||
chr13:79526977
|
T | A | 21 | a0001c0001t0004g0003a0001c0001t0004g0009a0001c0001t0004g0020others(18): Show | 27 | HG01069.hp1 HG01071.hp1 HG01243.hp2 others(24): Show |
intron_variant | MODIFIER | c.487+6002T>A | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 2/7 | chr13 | 79526977 | ||||||
chr13:79527250
|
A | G | 1 | a0001c0001t0013g0167 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.488-6073A>G | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 2/7 | chr13 | 79527250 | ||||||
chr13:79527274
|
A | G | 6 | a0001c0001t0002g0166a0001c0001t0002g0180a0001c0001t0002g0182others(3): Show | 6 | HG00544.hp2 HG02074.hp2 NA18962.hp1 others(3): Show |
intron_variant | MODIFIER | c.488-6049A>G | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 2/7 | chr13 | 79527274 | ||||||
chr13:79527372
|
T | C | 21 | a0001c0001t0004g0003a0001c0001t0004g0009a0001c0001t0004g0020others(18): Show | 27 | HG01069.hp1 HG01071.hp1 HG01243.hp2 others(24): Show |
intron_variant | MODIFIER | c.488-5951T>C | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 2/7 | chr13 | 79527372 | ||||||
chr13:79527399
|
A | G | 1 | a0001c0001t0002g0190 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.488-5924A>G | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 2/7 | chr13 | 79527399 | ||||||
chr13:79527549
|
T | C | 3 | a0003c0003t0005g0030a0003c0003t0005g0031a0003c0003t0005g0033 | 3 | HG02895.hp2 HG02897.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.488-5774T>C | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 2/7 | chr13 | 79527549 | ||||||
chr13:79527584
|
C | T | 1 | a0001c0001t0004g0140 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.488-5739C>T | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 2/7 | chr13 | 79527584 | ||||||
chr13:79527868
|
C | T | 1 | a0001c0001t0017g0094 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.488-5455C>T | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 2/7 | chr13 | 79527868 | ||||||
chr13:79527985
|
T | C | 242 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0011others(239): Show | 283 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(280): Show |
intron_variant | MODIFIER | c.488-5338T>C | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 2/7 | chr13 | 79527985 | ||||||
chr13:79528011
|
T | C | 242 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0011others(239): Show | 283 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(280): Show |
intron_variant | MODIFIER | c.488-5312T>C | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 2/7 | chr13 | 79528011 | ||||||
chr13:79528199
|
G | A | 3 | a0001c0001t0006g0074a0001c0001t0006g0090a0001c0001t0016g0110 | 3 | HG02129.hp2 NA19002.hp1 NA19078.hp2 |
intron_variant | MODIFIER | c.488-5124G>A | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 2/7 | chr13 | 79528199 | ||||||
chr13:79528925
|
A | G | 1 | a0003c0003t0005g0032 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.488-4398A>G | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 2/7 | chr13 | 79528925 | ||||||
chr13:79529094
|
C | T | 142 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0004others(139): Show | 171 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(168): Show |
intron_variant | MODIFIER | c.488-4229C>T | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 2/7 | chr13 | 79529094 | ||||||
chr13:79529143
|
T | C | 143 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0004others(140): Show | 172 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(169): Show |
intron_variant | MODIFIER | c.488-4180T>C | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 2/7 | chr13 | 79529143 | ||||||
chr13:79529211
|
T | C | 7 | a0001c0001t0003g0158a0001c0001t0003g0159a0001c0001t0003g0216others(4): Show | 7 | HG00735.hp2 HG01884.hp2 HG02145.hp2 others(4): Show |
intron_variant | MODIFIER | c.488-4112T>C | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 2/7 | chr13 | 79529211 | ||||||
chr13:79529318
|
A | G | 21 | a0001c0001t0004g0003a0001c0001t0004g0009a0001c0001t0004g0020others(18): Show | 27 | HG01069.hp1 HG01071.hp1 HG01243.hp2 others(24): Show |
intron_variant | MODIFIER | c.488-4005A>G | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 2/7 | chr13 | 79529318 | ||||||
chr13:79529551
|
G | A | 1 | a0001c0001t0001g0079 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.488-3772G>A | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 2/7 | chr13 | 79529551 | ||||||
chr13:79529950
|
A | G | 7 | a0001c0001t0003g0158a0001c0001t0003g0159a0001c0001t0003g0216others(4): Show | 7 | HG00735.hp2 HG01884.hp2 HG02145.hp2 others(4): Show |
intron_variant | MODIFIER | c.488-3373A>G | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 2/7 | chr13 | 79529950 | ||||||
chr13:79529988
|
G | A | 1 | a0001c0001t0002g0172 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.488-3335G>A | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 2/7 | chr13 | 79529988 | ||||||
chr13:79530170
|
A | G | 13 | a0001c0001t0015g0078a0003c0003t0005g0010a0003c0003t0005g0030others(10): Show | 14 | HG01981.hp2 HG02451.hp1 HG02486.hp1 others(11): Show |
intron_variant | MODIFIER | c.488-3153A>G | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 2/7 | chr13 | 79530170 | ||||||
chr13:79530279
|
A | T | 1 | a0001c0001t0001g0099 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.488-3044A>T | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 2/7 | chr13 | 79530279 | ||||||
chr13:79530464
|
A | G | 14 | a0001c0001t0015g0078a0003c0003t0005g0010a0003c0003t0005g0029others(11): Show | 15 | HG01981.hp2 HG02451.hp1 HG02486.hp1 others(12): Show |
intron_variant | MODIFIER | c.488-2859A>G | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 2/7 | chr13 | 79530464 | ||||||
chr13:79530633
|
G | C | 1 | a0001c0001t0002g0181 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.488-2690G>C | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 2/7 | chr13 | 79530633 | ||||||
chr13:79530807
|
T | C | 7 | a0001c0001t0003g0158a0001c0001t0003g0159a0001c0001t0003g0216others(4): Show | 7 | HG00735.hp2 HG01884.hp2 HG02145.hp2 others(4): Show |
intron_variant | MODIFIER | c.488-2516T>C | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 2/7 | chr13 | 79530807 | ||||||
chr13:79530872
|
C | T | 13 | a0002c0002t0003g0021a0002c0002t0003g0022a0002c0002t0003g0144others(10): Show | 15 | HG00140.hp1 HG00280.hp1 HG00733.hp1 others(12): Show |
intron_variant | MODIFIER | c.488-2451C>T | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 2/7 | chr13 | 79530872 | ||||||
chr13:79530930
|
C | G | 16 | a0001c0001t0015g0078a0003c0003t0005g0010a0003c0003t0005g0029others(13): Show | 17 | HG01981.hp2 HG02451.hp1 HG02486.hp1 others(14): Show |
intron_variant | MODIFIER | c.488-2393C>G | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 2/7 | chr13 | 79530930 | ||||||
chr13:79530992
|
G | T | 1 | a0001c0001t0003g0222 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.488-2331G>T | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 2/7 | chr13 | 79530992 | ||||||
chr13:79531050
|
T | A | 16 | a0001c0001t0015g0078a0003c0003t0005g0010a0003c0003t0005g0029others(13): Show | 17 | HG01981.hp2 HG02451.hp1 HG02486.hp1 others(14): Show |
intron_variant | MODIFIER | c.488-2273T>A | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 2/7 | chr13 | 79531050 | ||||||
chr13:79531583
|
C | T | 1 | a0002c0002t0003g0145 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.488-1740C>T | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 2/7 | chr13 | 79531583 | ||||||
chr13:79531934
|
C | T | 2 | a0003c0003t0010g0034a0003c0003t0010g0035 | 2 | HG02965.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.488-1389C>T | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 2/7 | chr13 | 79531934 | ||||||
chr13:79532036
|
C | T | 2 | a0001c0001t0004g0009a0001c0001t0004g0215 | 4 | HG01069.hp1 HG01071.hp1 HG01515.hp1 others(1): Show |
intron_variant | MODIFIER | c.488-1287C>T | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 2/7 | chr13 | 79532036 | ||||||
chr13:79532038
|
A | G | 18 | a0001c0001t0004g0003a0001c0001t0004g0009a0001c0001t0004g0020others(15): Show | 24 | HG01069.hp1 HG01071.hp1 HG01243.hp2 others(21): Show |
intron_variant | MODIFIER | c.488-1285A>G | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 2/7 | chr13 | 79532038 | ||||||
chr13:79532110
|
G | A | 1 | a0001c0001t0002g0192 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.488-1213G>A | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 2/7 | chr13 | 79532110 | ||||||
chr13:79532241
|
T | C | 2 | a0003c0003t0010g0034a0003c0003t0010g0035 | 2 | HG02965.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.488-1082T>C | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 2/7 | chr13 | 79532241 | ||||||
chr13:79532465
|
C | A | 16 | a0001c0001t0015g0078a0003c0003t0005g0010a0003c0003t0005g0029others(13): Show | 17 | HG01981.hp2 HG02451.hp1 HG02486.hp1 others(14): Show |
intron_variant | MODIFIER | c.488-858C>A | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 2/7 | chr13 | 79532465 | ||||||
chr13:79532802
|
T | C | 1 | a0001c0001t0011g0014 | 2 | HG01515.hp2 HG01517.hp1 |
intron_variant | MODIFIER | c.488-521T>C | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 2/7 | chr13 | 79532802 | ||||||
chr13:79533153
|
G | A | 16 | a0001c0001t0015g0078a0003c0003t0005g0010a0003c0003t0005g0029others(13): Show | 17 | HG01981.hp2 HG02451.hp1 HG02486.hp1 others(14): Show |
intron_variant | MODIFIER | c.488-170G>A | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 2/7 | chr13 | 79533153 | ||||||
chr13:79533197
|
A | G | 34 | a0001c0001t0003g0006a0001c0001t0003g0158a0001c0001t0003g0159others(31): Show | 39 | HG00140.hp1 HG00280.hp1 HG00733.hp1 others(36): Show |
intron_variant | MODIFIER | c.488-126A>G | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 2/7 | chr13 | 79533197 | ||||||
chr13:79533202
|
A | G | 1 | a0001c0001t0001g0089 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.488-121A>G | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 2/7 | chr13 | 79533202 | ||||||
chr13:79533510
|
T | G | 6 | a0001c0001t0003g0221a0001c0001t0003g0222a0001c0001t0003g0223others(3): Show | 6 | HG02109.hp1 HG02257.hp1 HG02976.hp2 others(3): Show |
intron_variant | MODIFIER | c.621+54T>G | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 3/7 | chr13 | 79533510 | ||||||
chr13:79533776
|
A | G | 2 | a0004c0004t0007g0127a0004c0004t0007g0141 | 2 | HG01952.hp1 HG02145.hp1 |
intron_variant | MODIFIER | c.621+320A>G | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 3/7 | chr13 | 79533776 | ||||||
chr13:79533776
|
ATGT | A | 16 | a0001c0001t0015g0078a0003c0003t0005g0010a0003c0003t0005g0029others(13): Show | 17 | HG01981.hp2 HG02451.hp1 HG02486.hp1 others(14): Show |
intron_variant | MODIFIER | c.621+322_621+324del others(3): Show |
NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr13 | 79533776 | |||||
chr13:79533780
|
T | A | 16 | a0001c0001t0015g0078a0003c0003t0005g0010a0003c0003t0005g0029others(13): Show | 17 | HG01981.hp2 HG02451.hp1 HG02486.hp1 others(14): Show |
intron_variant | MODIFIER | c.621+324T>A | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 3/7 | chr13 | 79533780 | ||||||
chr13:79533838
|
G | A | 16 | a0001c0001t0015g0078a0003c0003t0005g0010a0003c0003t0005g0029others(13): Show | 17 | HG01981.hp2 HG02451.hp1 HG02486.hp1 others(14): Show |
intron_variant | MODIFIER | c.621+382G>A | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 3/7 | chr13 | 79533838 | ||||||
chr13:79534326
|
G | A | 3 | a0003c0003t0005g0030a0003c0003t0005g0031a0003c0003t0005g0033 | 3 | HG02895.hp2 HG02897.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.621+870G>A | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 3/7 | chr13 | 79534326 | ||||||
chr13:79534350
|
G | GT | 122 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0011others(119): Show | 138 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(135): Show |
intron_variant | MODIFIER | c.621+917dupT | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr13 | 79534350 | |||||
chr13:79534350
|
G | GTT | 31 | a0001c0001t0001g0019a0001c0001t0001g0045a0001c0001t0001g0056others(28): Show | 33 | HG00408.hp1 HG01175.hp2 HG01261.hp2 others(30): Show |
intron_variant | MODIFIER | c.621+916_621+917dup others(2): Show |
NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr13 | 79534350 | |||||
chr13:79534490
|
T | C | 37 | a0001c0001t0004g0003a0001c0001t0004g0009a0001c0001t0004g0020others(34): Show | 44 | HG01069.hp1 HG01071.hp1 HG01243.hp2 others(41): Show |
intron_variant | MODIFIER | c.621+1034T>C | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 3/7 | chr13 | 79534490 | ||||||
chr13:79534607
|
T | A | 3 | a0001c0001t0004g0134a0001c0001t0004g0136a0001c0001t0019g0135 | 3 | HG02572.hp1 HG02615.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.621+1151T>A | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 3/7 | chr13 | 79534607 | ||||||
chr13:79535011
|
A | C | 1 | a0001c0001t0001g0112 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.621+1555A>C | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 3/7 | chr13 | 79535011 | ||||||
chr13:79535015
|
C | A | 2 | a0001c0001t0002g0166a0001c0001t0002g0180 | 2 | NA18962.hp1 NA19090.hp1 |
intron_variant | MODIFIER | c.621+1559C>A | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 3/7 | chr13 | 79535015 | ||||||
chr13:79535077
|
A | G | 1 | a0001c0001t0002g0172 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.621+1621A>G | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 3/7 | chr13 | 79535077 | ||||||
chr13:79535303
|
C | G | 1 | a0001c0001t0001g0104 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.621+1847C>G | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 3/7 | chr13 | 79535303 | ||||||
chr13:79535388
|
A | G | 16 | a0001c0001t0015g0078a0003c0003t0005g0010a0003c0003t0005g0029others(13): Show | 17 | HG01981.hp2 HG02451.hp1 HG02486.hp1 others(14): Show |
intron_variant | MODIFIER | c.621+1932A>G | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 3/7 | chr13 | 79535388 | ||||||
chr13:79535602
|
A | C | 1 | a0001c0001t0002g0230 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.621+2146A>C | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 3/7 | chr13 | 79535602 | ||||||
chr13:79535732
|
A | G | 70 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0004others(67): Show | 87 | HG00099.hp1 HG00323.hp1 HG00408.hp2 others(84): Show |
intron_variant | MODIFIER | c.621+2276A>G | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 3/7 | chr13 | 79535732 | ||||||
chr13:79535742
|
A | G | 1 | a0002c0002t0003g0152 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.621+2286A>G | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 3/7 | chr13 | 79535742 | ||||||
chr13:79535786
|
C | CA | 37 | a0001c0001t0004g0003a0001c0001t0004g0009a0001c0001t0004g0020others(34): Show | 44 | HG01069.hp1 HG01071.hp1 HG01243.hp2 others(41): Show |
intron_variant | MODIFIER | c.621+2338dupA | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr13 | 79535786 | |||||
chr13:79535906
|
A | G | 1 | a0001c0001t0002g0026 | 2 | NA18962.hp2 NA18975.hp2 |
intron_variant | MODIFIER | c.621+2450A>G | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 3/7 | chr13 | 79535906 | ||||||
chr13:79535923
|
T | C | 4 | a0001c0001t0002g0002a0001c0001t0002g0199a0001c0001t0002g0204others(1): Show | 7 | HG00741.hp2 HG01071.hp2 HG01109.hp2 others(4): Show |
intron_variant | MODIFIER | c.621+2467T>C | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 3/7 | chr13 | 79535923 | ||||||
chr13:79536012
|
A | G | 1 | a0001c0001t0009g0239 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.621+2556A>G | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 3/7 | chr13 | 79536012 | ||||||
chr13:79536029
|
TATAG | T | 21 | a0001c0001t0004g0003a0001c0001t0004g0009a0001c0001t0004g0020others(18): Show | 27 | HG01069.hp1 HG01071.hp1 HG01243.hp2 others(24): Show |
intron_variant | MODIFIER | c.621+2578_621+2581d others(6): Show |
NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr13 | 79536029 | |||||
chr13:79536082
|
A | G | 5 | a0001c0001t0001g0012a0001c0001t0001g0046a0001c0001t0001g0051others(2): Show | 6 | HG02630.hp2 HG02922.hp1 HG03225.hp1 others(3): Show |
intron_variant | MODIFIER | c.621+2626A>G | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 3/7 | chr13 | 79536082 | ||||||
chr13:79536158
|
T | C | 21 | a0001c0001t0004g0003a0001c0001t0004g0009a0001c0001t0004g0020others(18): Show | 27 | HG01069.hp1 HG01071.hp1 HG01243.hp2 others(24): Show |
intron_variant | MODIFIER | c.621+2702T>C | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 3/7 | chr13 | 79536158 | ||||||
chr13:79536191
|
A | G | 1 | a0001c0001t0001g0052 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.621+2735A>G | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 3/7 | chr13 | 79536191 | ||||||
chr13:79536239
|
A | C | 1 | a0001c0001t0002g0199 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.621+2783A>C | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 3/7 | chr13 | 79536239 | ||||||
chr13:79536454
|
A | G | 3 | a0001c0001t0004g0003a0001c0001t0004g0142a0001c0001t0004g0143 | 6 | HG02486.hp2 HG02622.hp1 HG03041.hp2 others(3): Show |
intron_variant | MODIFIER | c.621+2998A>G | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 3/7 | chr13 | 79536454 | ||||||
chr13:79536569
|
A | G | 12 | a0001c0001t0015g0078a0003c0003t0005g0010a0003c0003t0005g0030others(9): Show | 13 | HG01981.hp2 HG02451.hp1 HG02486.hp1 others(10): Show |
intron_variant | MODIFIER | c.621+3113A>G | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 3/7 | chr13 | 79536569 | ||||||
chr13:79536588
|
A | G | 2 | a0005c0005t0002g0155a0005c0005t0002g0157 | 2 | NA18906.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.622-3094A>G | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 3/7 | chr13 | 79536588 | ||||||
chr13:79536637
|
A | C | 3 | a0003c0003t0005g0030a0003c0003t0005g0031a0003c0003t0005g0033 | 3 | HG02895.hp2 HG02897.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.622-3045A>C | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 3/7 | chr13 | 79536637 | ||||||
chr13:79536980
|
A | G | 1 | a0001c0001t0021g0073 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.622-2702A>G | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 3/7 | chr13 | 79536980 | ||||||
chr13:79537027
|
G | A | 3 | a0001c0001t0001g0011a0001c0001t0001g0044a0001c0001t0001g0045 | 4 | HG00280.hp2 HG03017.hp2 HG03239.hp2 others(1): Show |
intron_variant | MODIFIER | c.622-2655G>A | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 3/7 | chr13 | 79537027 | ||||||
chr13:79537049
|
A | AT | 71 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0004others(68): Show | 88 | HG00099.hp1 HG00323.hp1 HG00408.hp2 others(85): Show |
intron_variant | MODIFIER | c.622-2620dupT | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr13 | 79537049 | |||||
chr13:79537049
|
AT | A | 6 | a0001c0001t0003g0221a0001c0001t0003g0222a0001c0001t0003g0223others(3): Show | 6 | HG02109.hp1 HG02257.hp1 HG02976.hp2 others(3): Show |
intron_variant | MODIFIER | c.622-2620delT | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr13 | 79537049 | |||||
chr13:79537100
|
T | G | 1 | a0001c0001t0018g0137 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.622-2582T>G | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 3/7 | chr13 | 79537100 | ||||||
chr13:79537114
|
T | G | 21 | a0001c0001t0004g0003a0001c0001t0004g0009a0001c0001t0004g0020others(18): Show | 27 | HG01069.hp1 HG01071.hp1 HG01243.hp2 others(24): Show |
intron_variant | MODIFIER | c.622-2568T>G | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 3/7 | chr13 | 79537114 | ||||||
chr13:79537231
|
T | C | 1 | a0001c0001t0001g0058 | 1 | NA18975.hp1 | intron_variant | MODIFIER | c.622-2451T>C | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 3/7 | chr13 | 79537231 | ||||||
chr13:79537317
|
G | T | 2 | a0001c0001t0002g0169a0001c0001t0002g0170 | 2 | HG03688.hp1 HG03831.hp1 |
intron_variant | MODIFIER | c.622-2365G>T | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 3/7 | chr13 | 79537317 | ||||||
chr13:79537980
|
T | TA | 71 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0004others(68): Show | 88 | HG00099.hp1 HG00323.hp1 HG00408.hp2 others(85): Show |
intron_variant | MODIFIER | c.622-1701dupA | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr13 | 79537980 | |||||
chr13:79538001
|
G | C | 143 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0004others(140): Show | 172 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(169): Show |
intron_variant | MODIFIER | c.622-1681G>C | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 3/7 | chr13 | 79538001 | ||||||
chr13:79538191
|
C | A | 21 | a0001c0001t0004g0003a0001c0001t0004g0009a0001c0001t0004g0020others(18): Show | 27 | HG01069.hp1 HG01071.hp1 HG01243.hp2 others(24): Show |
intron_variant | MODIFIER | c.622-1491C>A | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 3/7 | chr13 | 79538191 | ||||||
chr13:79538240
|
G | A | 1 | a0003c0003t0005g0029 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.622-1442G>A | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 3/7 | chr13 | 79538240 | ||||||
chr13:79538261
|
A | G | 3 | a0001c0001t0008g0130a0001c0001t0008g0131a0001c0001t0008g0132 | 3 | HG02723.hp1 HG02886.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.622-1421A>G | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 3/7 | chr13 | 79538261 | ||||||
chr13:79538552
|
G | A | 1 | a0001c0001t0001g0072 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.622-1130G>A | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 3/7 | chr13 | 79538552 | ||||||
chr13:79538622
|
G | A | 1 | a0001c0001t0001g0055 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.622-1060G>A | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 3/7 | chr13 | 79538622 | ||||||
chr13:79538673
|
C | T | 1 | a0001c0001t0001g0063 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.622-1009C>T | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 3/7 | chr13 | 79538673 | ||||||
chr13:79538686
|
G | C | 16 | a0001c0001t0015g0078a0003c0003t0005g0010a0003c0003t0005g0029others(13): Show | 17 | HG01981.hp2 HG02451.hp1 HG02486.hp1 others(14): Show |
intron_variant | MODIFIER | c.622-996G>C | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 3/7 | chr13 | 79538686 | ||||||
chr13:79538800
|
C | G | 1 | a0001c0001t0001g0089 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.622-882C>G | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 3/7 | chr13 | 79538800 | ||||||
chr13:79538804
|
A | G | 1 | a0001c0006t0006g0084 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.622-878A>G | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 3/7 | chr13 | 79538804 | ||||||
chr13:79538876
|
C | T | 1 | a0001c0001t0001g0081 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.622-806C>T | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 3/7 | chr13 | 79538876 | ||||||
chr13:79538979
|
T | C | 1 | a0002c0002t0003g0154 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.622-703T>C | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 3/7 | chr13 | 79538979 | ||||||
chr13:79538997
|
C | G | 1 | a0001c0001t0002g0234 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.622-685C>G | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 3/7 | chr13 | 79538997 | ||||||
chr13:79539067
|
CAT | C | 72 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0004others(69): Show | 89 | HG00099.hp1 HG00323.hp1 HG00408.hp2 others(86): Show |
intron_variant | MODIFIER | c.622-614_622-613del others(2): Show |
NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 3/7 | chr13 | 79539067 | ||||||
chr13:79539243
|
T | C | 21 | a0001c0001t0004g0003a0001c0001t0004g0009a0001c0001t0004g0020others(18): Show | 27 | HG01069.hp1 HG01071.hp1 HG01243.hp2 others(24): Show |
intron_variant | MODIFIER | c.622-439T>C | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 3/7 | chr13 | 79539243 | ||||||
chr13:79539517
|
G | C | 142 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0004others(139): Show | 171 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(168): Show |
intron_variant | MODIFIER | c.622-165G>C | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 3/7 | chr13 | 79539517 | ||||||
chr13:79540265
|
A | G | 5 | a0003c0003t0005g0010a0003c0003t0005g0036a0003c0003t0005g0037others(2): Show | 6 | HG01981.hp2 HG02451.hp1 HG02486.hp1 others(3): Show |
intron_variant | MODIFIER | c.715+490A>G | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 4/7 | chr13 | 79540265 | ||||||
chr13:79540346
|
T | G | 15 | a0001c0001t0004g0003a0001c0001t0004g0009a0001c0001t0004g0020others(12): Show | 21 | HG01069.hp1 HG01071.hp1 HG01243.hp2 others(18): Show |
intron_variant | MODIFIER | c.715+571T>G | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 4/7 | chr13 | 79540346 | ||||||
chr13:79540503
|
T | C | 2 | a0005c0005t0002g0155a0005c0005t0002g0157 | 2 | NA18906.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.715+728T>C | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 4/7 | chr13 | 79540503 | ||||||
chr13:79540621
|
A | G | 2 | a0001c0001t0002g0193a0001c0001t0002g0200 | 2 | NA18945.hp1 NA19066.hp2 |
intron_variant | MODIFIER | c.715+846A>G | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 4/7 | chr13 | 79540621 | ||||||
chr13:79540633
|
T | C | 2 | a0001c0001t0002g0193a0001c0001t0002g0200 | 2 | NA18945.hp1 NA19066.hp2 |
intron_variant | MODIFIER | c.715+858T>C | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 4/7 | chr13 | 79540633 | ||||||
chr13:79541197
|
A | G | 11 | a0001c0001t0001g0055a0001c0001t0001g0057a0001c0001t0001g0063others(8): Show | 11 | HG01109.hp1 HG01496.hp2 HG01884.hp1 others(8): Show |
intron_variant | MODIFIER | c.715+1422A>G | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 4/7 | chr13 | 79541197 | ||||||
chr13:79541254
|
G | A | 16 | a0001c0001t0015g0078a0003c0003t0005g0010a0003c0003t0005g0029others(13): Show | 17 | HG01981.hp2 HG02451.hp1 HG02486.hp1 others(14): Show |
intron_variant | MODIFIER | c.715+1479G>A | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 4/7 | chr13 | 79541254 | ||||||
chr13:79541330
|
T | C | 16 | a0001c0001t0015g0078a0003c0003t0005g0010a0003c0003t0005g0029others(13): Show | 17 | HG01981.hp2 HG02451.hp1 HG02486.hp1 others(14): Show |
intron_variant | MODIFIER | c.715+1555T>C | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 4/7 | chr13 | 79541330 | ||||||
chr13:79541333
|
A | G | 16 | a0001c0001t0015g0078a0003c0003t0005g0010a0003c0003t0005g0029others(13): Show | 17 | HG01981.hp2 HG02451.hp1 HG02486.hp1 others(14): Show |
intron_variant | MODIFIER | c.715+1558A>G | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 4/7 | chr13 | 79541333 | ||||||
chr13:79541479
|
A | G | 2 | a0003c0003t0005g0030a0003c0003t0005g0031 | 2 | HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.715+1704A>G | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 4/7 | chr13 | 79541479 | ||||||
chr13:79541980
|
A | G | 12 | a0001c0001t0003g0006a0001c0001t0003g0158a0001c0001t0003g0159others(9): Show | 15 | HG00735.hp2 HG01884.hp2 HG02055.hp1 others(12): Show |
intron_variant | MODIFIER | c.716-1578A>G | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 4/7 | chr13 | 79541980 | ||||||
chr13:79542022
|
C | T | 2 | a0001c0001t0004g0134a0001c0001t0004g0136 | 2 | HG02572.hp1 HG02615.hp1 |
intron_variant | MODIFIER | c.716-1536C>T | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 4/7 | chr13 | 79542022 | ||||||
chr13:79542487
|
G | T | 1 | a0001c0001t0002g0165 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.716-1071G>T | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 4/7 | chr13 | 79542487 | ||||||
chr13:79542505
|
G | GTTTT | 13 | a0001c0001t0015g0078a0003c0003t0005g0010a0003c0003t0005g0032others(10): Show | 14 | HG01981.hp2 HG02451.hp1 HG02486.hp1 others(11): Show |
intron_variant | MODIFIER | c.716-1050_716-1047d others(6): Show |
NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr13 | 79542505 | |||||
chr13:79542510
|
T | C | 5 | a0001c0001t0001g0012a0001c0001t0001g0046a0001c0001t0001g0051others(2): Show | 6 | HG02630.hp2 HG02922.hp1 HG03225.hp1 others(3): Show |
intron_variant | MODIFIER | c.716-1048T>C | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 4/7 | chr13 | 79542510 | ||||||
chr13:79542512
|
G | T | 15 | a0001c0001t0015g0078a0003c0003t0005g0010a0003c0003t0005g0030others(12): Show | 16 | HG01981.hp2 HG02451.hp1 HG02486.hp1 others(13): Show |
intron_variant | MODIFIER | c.716-1046G>T | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 4/7 | chr13 | 79542512 | ||||||
chr13:79542556
|
T | C | 1 | a0001c0001t0002g0194 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.716-1002T>C | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 4/7 | chr13 | 79542556 | ||||||
chr13:79542624
|
A | G | 4 | a0001c0001t0002g0002a0001c0001t0002g0199a0001c0001t0002g0204others(1): Show | 7 | HG00741.hp2 HG01071.hp2 HG01109.hp2 others(4): Show |
intron_variant | MODIFIER | c.716-934A>G | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 4/7 | chr13 | 79542624 | ||||||
chr13:79542666
|
T | C | 21 | a0001c0001t0004g0003a0001c0001t0004g0009a0001c0001t0004g0020others(18): Show | 27 | HG01069.hp1 HG01071.hp1 HG01243.hp2 others(24): Show |
intron_variant | MODIFIER | c.716-892T>C | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 4/7 | chr13 | 79542666 | ||||||
chr13:79542764
|
C | T | 1 | a0003c0003t0005g0042 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.716-794C>T | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 4/7 | chr13 | 79542764 | ||||||
chr13:79542844
|
C | G | 157 | a0001c0001t0001g0055a0001c0001t0001g0057a0001c0001t0001g0063others(154): Show | 186 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(183): Show |
intron_variant | MODIFIER | c.716-714C>G | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 4/7 | chr13 | 79542844 | ||||||
chr13:79542883
|
CT | C | 16 | a0001c0001t0015g0078a0003c0003t0005g0010a0003c0003t0005g0029others(13): Show | 17 | HG01981.hp2 HG02451.hp1 HG02486.hp1 others(14): Show |
intron_variant | MODIFIER | c.716-664delT | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr13 | 79542883 | |||||
chr13:79542991
|
C | T | 2 | a0003c0003t0010g0034a0003c0003t0010g0035 | 2 | HG02965.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.716-567C>T | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 4/7 | chr13 | 79542991 | ||||||
chr13:79543171
|
C | T | 2 | a0005c0005t0002g0155a0005c0005t0002g0157 | 2 | NA18906.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.716-387C>T | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 4/7 | chr13 | 79543171 | ||||||
chr13:79543296
|
A | T | 16 | a0001c0001t0015g0078a0003c0003t0005g0010a0003c0003t0005g0029others(13): Show | 17 | HG01981.hp2 HG02451.hp1 HG02486.hp1 others(14): Show |
intron_variant | MODIFIER | c.716-262A>T | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 4/7 | chr13 | 79543296 | ||||||
chr13:79543916
|
T | C | 14 | a0001c0001t0015g0078a0003c0003t0005g0010a0003c0003t0005g0029others(11): Show | 15 | HG01981.hp2 HG02451.hp1 HG02486.hp1 others(12): Show |
intron_variant | MODIFIER | c.840+234T>C | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 5/7 | chr13 | 79543916 | ||||||
chr13:79543946
|
CTTTA | C | 26 | a0001c0001t0001g0011a0001c0001t0001g0016a0001c0001t0001g0017others(23): Show | 31 | HG00280.hp2 HG00544.hp1 HG01258.hp1 others(28): Show |
intron_variant | MODIFIER | c.840+269_840+272del others(4): Show |
NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr13 | 79543946 | |||||
chr13:79543965
|
G | A | 1 | a0001c0001t0001g0105 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.840+283G>A | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 5/7 | chr13 | 79543965 | ||||||
chr13:79544161
|
A | T | 8 | a0001c0001t0004g0003a0001c0001t0004g0020a0001c0001t0004g0138others(5): Show | 12 | HG01243.hp2 HG02486.hp2 HG02622.hp1 others(9): Show |
intron_variant | MODIFIER | c.840+479A>T | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 5/7 | chr13 | 79544161 | ||||||
chr13:79544390
|
AG | A | 3 | a0001c0001t0002g0024a0001c0001t0002g0171a0001c0001t0002g0240 | 4 | NA18941.hp2 NA18944.hp1 NA18959.hp2 others(1): Show |
intron_variant | MODIFIER | c.840+709delG | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 5/7 | chr13 | 79544390 | ||||||
chr13:79544428
|
G | A | 2 | a0001c0001t0006g0090a0001c0001t0016g0110 | 2 | NA19002.hp1 NA19078.hp2 |
intron_variant | MODIFIER | c.840+746G>A | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 5/7 | chr13 | 79544428 | ||||||
chr13:79544492
|
G | GT | 18 | a0001c0001t0004g0003a0001c0001t0004g0009a0001c0001t0004g0020others(15): Show | 24 | HG01069.hp1 HG01071.hp1 HG01243.hp2 others(21): Show |
intron_variant | MODIFIER | c.840+824dupT | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr13 | 79544492 | |||||
chr13:79544492
|
GT | G | 19 | a0001c0001t0001g0080a0001c0001t0001g0089a0001c0001t0001g0091others(16): Show | 20 | HG01256.hp1 HG01981.hp2 HG02258.hp1 others(17): Show |
intron_variant | MODIFIER | c.840+824delT | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr13 | 79544492 | |||||
chr13:79544516
|
A | G | 1 | a0001c0001t0001g0055 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.840+834A>G | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 5/7 | chr13 | 79544516 | ||||||
chr13:79544691
|
A | G | 1 | a0001c0001t0006g0092 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.840+1009A>G | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 5/7 | chr13 | 79544691 | ||||||
chr13:79544692
|
T | C | 21 | a0001c0001t0004g0003a0001c0001t0004g0009a0001c0001t0004g0020others(18): Show | 27 | HG01069.hp1 HG01071.hp1 HG01243.hp2 others(24): Show |
intron_variant | MODIFIER | c.840+1010T>C | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 5/7 | chr13 | 79544692 | ||||||
chr13:79544737
|
T | C | 1 | a0001c0001t0008g0131 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.840+1055T>C | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 5/7 | chr13 | 79544737 | ||||||
chr13:79544797
|
T | C | 14 | a0001c0001t0015g0078a0003c0003t0005g0010a0003c0003t0005g0029others(11): Show | 15 | HG01981.hp2 HG02451.hp1 HG02486.hp1 others(12): Show |
intron_variant | MODIFIER | c.840+1115T>C | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 5/7 | chr13 | 79544797 | ||||||
chr13:79545000
|
A | T | 14 | a0001c0001t0015g0078a0003c0003t0005g0010a0003c0003t0005g0029others(11): Show | 15 | HG01981.hp2 HG02451.hp1 HG02486.hp1 others(12): Show |
intron_variant | MODIFIER | c.840+1318A>T | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 5/7 | chr13 | 79545000 | ||||||
chr13:79545089
|
A | G | 1 | a0001c0001t0001g0082 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.840+1407A>G | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 5/7 | chr13 | 79545089 | ||||||
chr13:79545124
|
T | A | 2 | a0003c0003t0010g0034a0003c0003t0010g0035 | 2 | HG02965.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.840+1442T>A | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 5/7 | chr13 | 79545124 | ||||||
chr13:79545180
|
C | T | 32 | a0001c0001t0003g0006a0001c0001t0003g0158a0001c0001t0003g0159others(29): Show | 37 | HG00140.hp1 HG00280.hp1 HG00733.hp1 others(34): Show |
intron_variant | MODIFIER | c.840+1498C>T | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 5/7 | chr13 | 79545180 | ||||||
chr13:79545181
|
A | G | 1 | a0001c0001t0004g0133 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.840+1499A>G | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 5/7 | chr13 | 79545181 | ||||||
chr13:79545287
|
T | C | 16 | a0001c0001t0015g0078a0003c0003t0005g0010a0003c0003t0005g0029others(13): Show | 17 | HG01981.hp2 HG02451.hp1 HG02486.hp1 others(14): Show |
intron_variant | MODIFIER | c.840+1605T>C | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 5/7 | chr13 | 79545287 | ||||||
chr13:79545604
|
A | G | 16 | a0001c0001t0015g0078a0003c0003t0005g0010a0003c0003t0005g0029others(13): Show | 17 | HG01981.hp2 HG02451.hp1 HG02486.hp1 others(14): Show |
intron_variant | MODIFIER | c.840+1922A>G | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 5/7 | chr13 | 79545604 | ||||||
chr13:79545610
|
G | T | 2 | a0003c0003t0010g0034a0003c0003t0010g0035 | 2 | HG02965.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.840+1928G>T | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 5/7 | chr13 | 79545610 | ||||||
chr13:79545631
|
C | T | 16 | a0001c0001t0015g0078a0003c0003t0005g0010a0003c0003t0005g0029others(13): Show | 17 | HG01981.hp2 HG02451.hp1 HG02486.hp1 others(14): Show |
intron_variant | MODIFIER | c.840+1949C>T | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 5/7 | chr13 | 79545631 | ||||||
chr13:79545676
|
A | G | 6 | a0001c0001t0001g0016a0001c0001t0001g0098a0001c0001t0001g0099others(3): Show | 7 | HG01258.hp1 HG01346.hp1 HG01934.hp1 others(4): Show |
intron_variant | MODIFIER | c.840+1994A>G | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 5/7 | chr13 | 79545676 | ||||||
chr13:79545759
|
C | T | 1 | a0001c0001t0002g0186 | 1 | NA19075.hp2 | intron_variant | MODIFIER | c.840+2077C>T | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 5/7 | chr13 | 79545759 | ||||||
chr13:79545797
|
T | A | 1 | a0001c0001t0001g0060 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.840+2115T>A | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 5/7 | chr13 | 79545797 | ||||||
chr13:79545938
|
G | A | 2 | a0002c0002t0003g0021a0002c0002t0003g0144 | 3 | HG02698.hp1 HG03490.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.840+2256G>A | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 5/7 | chr13 | 79545938 | ||||||
chr13:79546020
|
G | A | 21 | a0001c0001t0004g0003a0001c0001t0004g0009a0001c0001t0004g0020others(18): Show | 27 | HG01069.hp1 HG01071.hp1 HG01243.hp2 others(24): Show |
intron_variant | MODIFIER | c.841-2308G>A | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 5/7 | chr13 | 79546020 | ||||||
chr13:79546072
|
A | G | 1 | a0001c0001t0002g0236 | 1 | NA18987.hp2 | intron_variant | MODIFIER | c.841-2256A>G | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 5/7 | chr13 | 79546072 | ||||||
chr13:79546128
|
T | C | 21 | a0001c0001t0004g0003a0001c0001t0004g0009a0001c0001t0004g0020others(18): Show | 27 | HG01069.hp1 HG01071.hp1 HG01243.hp2 others(24): Show |
intron_variant | MODIFIER | c.841-2200T>C | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 5/7 | chr13 | 79546128 | ||||||
chr13:79546145
|
G | A | 18 | a0001c0001t0004g0003a0001c0001t0004g0009a0001c0001t0004g0020others(15): Show | 24 | HG01069.hp1 HG01071.hp1 HG01243.hp2 others(21): Show |
intron_variant | MODIFIER | c.841-2183G>A | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 5/7 | chr13 | 79546145 | ||||||
chr13:79546223
|
TA | T | 72 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0004others(69): Show | 89 | HG00099.hp1 HG00323.hp1 HG00408.hp2 others(86): Show |
intron_variant | MODIFIER | c.841-2103delA | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr13 | 79546223 | |||||
chr13:79546248
|
G | C | 1 | a0003c0003t0005g0032 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.841-2080G>C | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 5/7 | chr13 | 79546248 | ||||||
chr13:79546272
|
C | T | 6 | a0001c0001t0003g0221a0001c0001t0003g0222a0001c0001t0003g0223others(3): Show | 6 | HG02109.hp1 HG02257.hp1 HG02976.hp2 others(3): Show |
intron_variant | MODIFIER | c.841-2056C>T | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 5/7 | chr13 | 79546272 | ||||||
chr13:79546541
|
T | C | 1 | a0003c0003t0005g0032 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.841-1787T>C | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 5/7 | chr13 | 79546541 | ||||||
chr13:79547000
|
T | G | 242 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0011others(239): Show | 283 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(280): Show |
intron_variant | MODIFIER | c.841-1328T>G | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 5/7 | chr13 | 79547000 | ||||||
chr13:79547049
|
A | T | 15 | a0003c0003t0005g0010a0003c0003t0005g0029a0003c0003t0005g0030others(12): Show | 16 | HG01981.hp2 HG02451.hp1 HG02486.hp1 others(13): Show |
intron_variant | MODIFIER | c.841-1279A>T | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 5/7 | chr13 | 79547049 | ||||||
chr13:79547096
|
A | C | 1 | a0001c0001t0001g0162 | 1 | HG01517.hp2 | intron_variant | MODIFIER | c.841-1232A>C | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 5/7 | chr13 | 79547096 | ||||||
chr13:79547227
|
A | C | 29 | a0001c0001t0002g0004a0001c0001t0002g0005a0001c0001t0002g0024others(26): Show | 36 | HG00099.hp1 HG00323.hp1 HG00408.hp2 others(33): Show |
intron_variant | MODIFIER | c.841-1101A>C | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 5/7 | chr13 | 79547227 | ||||||
chr13:79547281
|
C | T | 15 | a0003c0003t0005g0010a0003c0003t0005g0029a0003c0003t0005g0030others(12): Show | 16 | HG01981.hp2 HG02451.hp1 HG02486.hp1 others(13): Show |
intron_variant | MODIFIER | c.841-1047C>T | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 5/7 | chr13 | 79547281 | ||||||
chr13:79547339
|
A | G | 1 | a0001c0001t0002g0232 | 1 | NA19080.hp2 | intron_variant | MODIFIER | c.841-989A>G | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 5/7 | chr13 | 79547339 | ||||||
chr13:79547415
|
G | A | 1 | a0003c0003t0005g0029 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.841-913G>A | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 5/7 | chr13 | 79547415 | ||||||
chr13:79547610
|
C | G | 1 | a0001c0001t0001g0052 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.841-718C>G | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 5/7 | chr13 | 79547610 | ||||||
chr13:79547614
|
G | C | 2 | a0003c0003t0010g0034a0003c0003t0010g0035 | 2 | HG02965.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.841-714G>C | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 5/7 | chr13 | 79547614 | ||||||
chr13:79547675
|
A | G | 2 | a0003c0003t0010g0034a0003c0003t0010g0035 | 2 | HG02965.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.841-653A>G | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 5/7 | chr13 | 79547675 | ||||||
chr13:79547839
|
A | T | 1 | a0001c0001t0006g0092 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.841-489A>T | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 5/7 | chr13 | 79547839 | ||||||
chr13:79547847
|
T | C | 1 | a0002c0002t0003g0153 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.841-481T>C | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 5/7 | chr13 | 79547847 | ||||||
chr13:79548152
|
C | G | 1 | a0003c0003t0005g0029 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.841-176C>G | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 5/7 | chr13 | 79548152 | ||||||
chr13:79548214
|
C | T | 15 | a0003c0003t0005g0010a0003c0003t0005g0029a0003c0003t0005g0030others(12): Show | 16 | HG01981.hp2 HG02451.hp1 HG02486.hp1 others(13): Show |
intron_variant | MODIFIER | c.841-114C>T | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 5/7 | chr13 | 79548214 | ||||||
chr13:79548300
|
G | A | 1 | a0001c0001t0012g0177 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.841-28G>A | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 5/7 | chr13 | 79548300 | ||||||
chr13:79548894
|
G | A | 4 | a0001c0001t0003g0006a0001c0001t0003g0161a0001c0001t0003g0227others(1): Show | 7 | HG02257.hp2 HG02572.hp2 HG02922.hp2 others(4): Show |
intron_variant | MODIFIER | c.907+500G>A | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 6/7 | chr13 | 79548894 | ||||||
chr13:79549009
|
A | G | 1 | a0001c0001t0001g0098 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.907+615A>G | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 6/7 | chr13 | 79549009 | ||||||
chr13:79549038
|
A | G | 2 | a0001c0001t0001g0019a0001c0001t0001g0106 | 3 | NA18979.hp1 NA18986.hp1 NA19090.hp2 |
intron_variant | MODIFIER | c.907+644A>G | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 6/7 | chr13 | 79549038 | ||||||
chr13:79549299
|
T | C | 1 | a0001c0001t0001g0081 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.907+905T>C | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 6/7 | chr13 | 79549299 | ||||||
chr13:79549382
|
T | G | 2 | a0001c0001t0003g0216a0001c0001t0003g0217 | 2 | HG02145.hp2 HG02451.hp2 |
intron_variant | MODIFIER | c.907+988T>G | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 6/7 | chr13 | 79549382 | ||||||
chr13:79549528
|
A | C | 1 | a0001c0001t0003g0228 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.907+1134A>C | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 6/7 | chr13 | 79549528 | ||||||
chr13:79549849
|
A | C | 143 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0004others(140): Show | 172 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(169): Show |
intron_variant | MODIFIER | c.908-1168A>C | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 6/7 | chr13 | 79549849 | ||||||
chr13:79549961
|
C | T | 17 | a0001c0001t0004g0003a0001c0001t0004g0009a0001c0001t0004g0020others(14): Show | 23 | HG01069.hp1 HG01071.hp1 HG01243.hp2 others(20): Show |
intron_variant | MODIFIER | c.908-1056C>T | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 6/7 | chr13 | 79549961 | ||||||
chr13:79550205
|
C | T | 1 | a0001c0001t0001g0051 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.908-812C>T | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 6/7 | chr13 | 79550205 | ||||||
chr13:79550241
|
T | G | 1 | a0003c0003t0005g0029 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.908-776T>G | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 6/7 | chr13 | 79550241 | ||||||
chr13:79550572
|
T | C | 143 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0004others(140): Show | 172 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(169): Show |
intron_variant | MODIFIER | c.908-445T>C | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 6/7 | chr13 | 79550572 | ||||||
chr13:79550582
|
T | C | 143 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0004others(140): Show | 172 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(169): Show |
intron_variant | MODIFIER | c.908-435T>C | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 6/7 | chr13 | 79550582 | ||||||
chr13:79550906
|
A | T | 1 | a0001c0001t0001g0121 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.908-111A>T | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 6/7 | chr13 | 79550906 | ||||||
chr13:79551551
|
C | T | 1 | a0001c0001t0001g0015 | 2 | HG00733.hp2 HG00738.hp1 |
intron_variant | MODIFIER | c.*2+429C>T | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 7/7 | chr13 | 79551551 | ||||||
chr13:79551603
|
A | G | 1 | a0001c0001t0001g0059 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.*2+481A>G | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 7/7 | chr13 | 79551603 | ||||||
chr13:79551768
|
T | C | 2 | a0005c0005t0002g0155a0005c0005t0002g0157 | 2 | NA18906.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.*2+646T>C | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 7/7 | chr13 | 79551768 | ||||||
chr13:79551801
|
C | T | 2 | a0003c0003t0010g0034a0003c0003t0010g0035 | 2 | HG02965.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.*2+679C>T | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 7/7 | chr13 | 79551801 | ||||||
chr13:79551850
|
A | G | 1 | a0001c0001t0001g0048 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.*3-666A>G | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 7/7 | chr13 | 79551850 | ||||||
chr13:79551979
|
C | G | 1 | a0001c0001t0003g0224 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.*3-537C>G | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 7/7 | chr13 | 79551979 | ||||||
chr13:79552026
|
A | G | 1 | a0001c0001t0003g0224 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.*3-490A>G | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 7/7 | chr13 | 79552026 | ||||||
chr13:79552213
|
C | G | 15 | a0003c0003t0005g0010a0003c0003t0005g0029a0003c0003t0005g0030others(12): Show | 16 | HG01981.hp2 HG02451.hp1 HG02486.hp1 others(13): Show |
intron_variant | MODIFIER | c.*3-303C>G | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 7/7 | chr13 | 79552213 | ||||||
chr13:79552355
|
A | G | 1 | a0001c0001t0019g0135 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.*3-161A>G | NDFIP2 | ENSG00000102471.16 | transcript | ENST00000218652.12 | protein_coding | 7/7 | chr13 | 79552355 |