geneid | 23386 |
---|---|
ensemblid | ENSG00000015676.18 |
hgncid | 22208 |
symbol | NUDCD3 |
name | NudC domain containing 3 |
refseq_nuc | NM_015332.4 |
refseq_prot | NP_056147.2 |
ensembl_nuc | ENST00000355451.8 |
ensembl_prot | ENSP00000347626.6 |
mane_status | MANE Select |
chr | chr7 |
start | 44379119 |
end | 44490658 |
strand | - |
ver | v1.2 |
region | chr7:44379119-44490658 |
region5000 | chr7:44374119-44495658 |
regionname0 | NUDCD3_chr7_44379119_44490658 |
regionname5000 | NUDCD3_chr7_44374119_44495658 |
ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 1/0 | 361 | 189 | 41 | 37 | 70 | 10 | 30 | 48 | NUDCD3_chr7_44374119_44495658 | NUDCD3 | copy fasta | chr7 | 44374119 | 44495658 |
a0002 | 0/0 | 361 | 28 | 19 | 6 | 0 | 0 | 3 | 0 | NUDCD3_chr7_44374119_44495658 | NUDCD3 | copy fasta | chr7 | 44374119 | 44495658 |
a0003 | 0/1 | 361 | 17 | 0 | 4 | 3 | 4 | 5 | 2 | NUDCD3_chr7_44374119_44495658 | NUDCD3 | copy fasta | chr7 | 44374119 | 44495658 |
a0004 | 0/0 | 361 | 3 | 2 | 1 | 0 | 0 | 0 | 0 | NUDCD3_chr7_44374119_44495658 | NUDCD3 | copy fasta | chr7 | 44374119 | 44495658 |
a0005 | 0/0 | 361 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | NUDCD3_chr7_44374119_44495658 | NUDCD3 | copy fasta | chr7 | 44374119 | 44495658 |
chapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
c0001 | 1/0 | 1086 | 188 | 41 | 37 | 69 | 10 | 30 | NUDCD3_chr7_44374119_44495658 | NUDCD3 | copy fasta | chr7 | 44374119 | 44495658 |
c0002 | 0/0 | 1086 | 26 | 17 | 6 | 0 | 0 | 3 | NUDCD3_chr7_44374119_44495658 | NUDCD3 | copy fasta | chr7 | 44374119 | 44495658 |
c0003 | 0/1 | 1086 | 17 | 0 | 4 | 3 | 4 | 5 | NUDCD3_chr7_44374119_44495658 | NUDCD3 | copy fasta | chr7 | 44374119 | 44495658 |
c0004 | 0/0 | 1086 | 3 | 2 | 1 | 0 | 0 | 0 | NUDCD3_chr7_44374119_44495658 | NUDCD3 | copy fasta | chr7 | 44374119 | 44495658 |
c0005 | 0/0 | 1086 | 2 | 2 | 0 | 0 | 0 | 0 | NUDCD3_chr7_44374119_44495658 | NUDCD3 | copy fasta | chr7 | 44374119 | 44495658 |
c0006 | 0/0 | 1086 | 1 | 0 | 0 | 1 | 0 | 0 | NUDCD3_chr7_44374119_44495658 | NUDCD3 | copy fasta | chr7 | 44374119 | 44495658 |
c0007 | 0/0 | 1086 | 1 | 0 | 0 | 1 | 0 | 0 | NUDCD3_chr7_44374119_44495658 | NUDCD3 | copy fasta | chr7 | 44374119 | 44495658 |
thapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
t0001 | 0/0 | 6951 | 130 | 34 | 23 | 49 | 5 | 19 | NUDCD3_chr7_44374119_44495658 | NUDCD3 | copy fasta | chr7 | 44374119 | 44495658 |
t0002 | 1/0 | 6951 | 25 | 0 | 4 | 9 | 4 | 7 | NUDCD3_chr7_44374119_44495658 | NUDCD3 | copy fasta | chr7 | 44374119 | 44495658 |
t0003 | 0/0 | 6952 | 13 | 2 | 2 | 8 | 1 | 0 | NUDCD3_chr7_44374119_44495658 | NUDCD3 | copy fasta | chr7 | 44374119 | 44495658 |
t0004 | 0/0 | 6951 | 8 | 1 | 4 | 0 | 0 | 3 | NUDCD3_chr7_44374119_44495658 | NUDCD3 | copy fasta | chr7 | 44374119 | 44495658 |
t0005 | 0/0 | 6951 | 8 | 0 | 3 | 0 | 3 | 2 | NUDCD3_chr7_44374119_44495658 | NUDCD3 | copy fasta | chr7 | 44374119 | 44495658 |
t0006 | 0/0 | 6951 | 4 | 0 | 0 | 3 | 0 | 1 | NUDCD3_chr7_44374119_44495658 | NUDCD3 | copy fasta | chr7 | 44374119 | 44495658 |
t0007 | 0/0 | 6949 | 3 | 3 | 0 | 0 | 0 | 0 | NUDCD3_chr7_44374119_44495658 | NUDCD3 | copy fasta | chr7 | 44374119 | 44495658 |
t0008 | 0/0 | 6949 | 3 | 3 | 0 | 0 | 0 | 0 | NUDCD3_chr7_44374119_44495658 | NUDCD3 | copy fasta | chr7 | 44374119 | 44495658 |
t0009 | 0/1 | 6951 | 3 | 0 | 1 | 0 | 0 | 1 | NUDCD3_chr7_44374119_44495658 | NUDCD3 | copy fasta | chr7 | 44374119 | 44495658 |
t0010 | 0/0 | 6949 | 2 | 1 | 1 | 0 | 0 | 0 | NUDCD3_chr7_44374119_44495658 | NUDCD3 | copy fasta | chr7 | 44374119 | 44495658 |
t0011 | 0/0 | 6949 | 2 | 2 | 0 | 0 | 0 | 0 | NUDCD3_chr7_44374119_44495658 | NUDCD3 | copy fasta | chr7 | 44374119 | 44495658 |
t0012 | 0/0 | 6952 | 2 | 2 | 0 | 0 | 0 | 0 | NUDCD3_chr7_44374119_44495658 | NUDCD3 | copy fasta | chr7 | 44374119 | 44495658 |
t0013 | 0/0 | 6951 | 2 | 2 | 0 | 0 | 0 | 0 | NUDCD3_chr7_44374119_44495658 | NUDCD3 | copy fasta | chr7 | 44374119 | 44495658 |
t0014 | 0/0 | 6952 | 2 | 0 | 1 | 0 | 0 | 1 | NUDCD3_chr7_44374119_44495658 | NUDCD3 | copy fasta | chr7 | 44374119 | 44495658 |
t0015 | 0/0 | 6951 | 2 | 0 | 2 | 0 | 0 | 0 | NUDCD3_chr7_44374119_44495658 | NUDCD3 | copy fasta | chr7 | 44374119 | 44495658 |
t0016 | 0/0 | 6951 | 2 | 0 | 2 | 0 | 0 | 0 | NUDCD3_chr7_44374119_44495658 | NUDCD3 | copy fasta | chr7 | 44374119 | 44495658 |
t0017 | 0/0 | 6951 | 2 | 2 | 0 | 0 | 0 | 0 | NUDCD3_chr7_44374119_44495658 | NUDCD3 | copy fasta | chr7 | 44374119 | 44495658 |
t0018 | 0/0 | 6951 | 2 | 2 | 0 | 0 | 0 | 0 | NUDCD3_chr7_44374119_44495658 | NUDCD3 | copy fasta | chr7 | 44374119 | 44495658 |
t0019 | 0/0 | 6951 | 2 | 0 | 0 | 0 | 1 | 1 | NUDCD3_chr7_44374119_44495658 | NUDCD3 | copy fasta | chr7 | 44374119 | 44495658 |
t0020 | 0/0 | 6951 | 1 | 1 | 0 | 0 | 0 | 0 | NUDCD3_chr7_44374119_44495658 | NUDCD3 | copy fasta | chr7 | 44374119 | 44495658 |
t0021 | 0/0 | 6951 | 1 | 1 | 0 | 0 | 0 | 0 | NUDCD3_chr7_44374119_44495658 | NUDCD3 | copy fasta | chr7 | 44374119 | 44495658 |
t0022 | 0/0 | 6951 | 1 | 0 | 1 | 0 | 0 | 0 | NUDCD3_chr7_44374119_44495658 | NUDCD3 | copy fasta | chr7 | 44374119 | 44495658 |
t0023 | 0/0 | 6951 | 1 | 1 | 0 | 0 | 0 | 0 | NUDCD3_chr7_44374119_44495658 | NUDCD3 | copy fasta | chr7 | 44374119 | 44495658 |
t0024 | 0/0 | 6951 | 1 | 0 | 0 | 0 | 0 | 1 | NUDCD3_chr7_44374119_44495658 | NUDCD3 | copy fasta | chr7 | 44374119 | 44495658 |
t0025 | 0/0 | 6951 | 1 | 0 | 0 | 0 | 0 | 1 | NUDCD3_chr7_44374119_44495658 | NUDCD3 | copy fasta | chr7 | 44374119 | 44495658 |
t0026 | 0/0 | 6951 | 1 | 0 | 1 | 0 | 0 | 0 | NUDCD3_chr7_44374119_44495658 | NUDCD3 | copy fasta | chr7 | 44374119 | 44495658 |
t0027 | 0/0 | 6951 | 1 | 1 | 0 | 0 | 0 | 0 | NUDCD3_chr7_44374119_44495658 | NUDCD3 | copy fasta | chr7 | 44374119 | 44495658 |
t0028 | 0/0 | 6952 | 1 | 0 | 0 | 1 | 0 | 0 | NUDCD3_chr7_44374119_44495658 | NUDCD3 | copy fasta | chr7 | 44374119 | 44495658 |
t0029 | 0/0 | 6951 | 1 | 1 | 0 | 0 | 0 | 0 | NUDCD3_chr7_44374119_44495658 | NUDCD3 | copy fasta | chr7 | 44374119 | 44495658 |
t0030 | 0/0 | 6951 | 1 | 0 | 1 | 0 | 0 | 0 | NUDCD3_chr7_44374119_44495658 | NUDCD3 | copy fasta | chr7 | 44374119 | 44495658 |
t0031 | 0/0 | 6951 | 1 | 0 | 1 | 0 | 0 | 0 | NUDCD3_chr7_44374119_44495658 | NUDCD3 | copy fasta | chr7 | 44374119 | 44495658 |
t0032 | 0/0 | 6951 | 1 | 0 | 1 | 0 | 0 | 0 | NUDCD3_chr7_44374119_44495658 | NUDCD3 | copy fasta | chr7 | 44374119 | 44495658 |
t0033 | 0/0 | 6951 | 1 | 1 | 0 | 0 | 0 | 0 | NUDCD3_chr7_44374119_44495658 | NUDCD3 | copy fasta | chr7 | 44374119 | 44495658 |
t0034 | 0/0 | 6952 | 1 | 0 | 0 | 1 | 0 | 0 | NUDCD3_chr7_44374119_44495658 | NUDCD3 | copy fasta | chr7 | 44374119 | 44495658 |
t0035 | 0/0 | 6951 | 1 | 0 | 0 | 1 | 0 | 0 | NUDCD3_chr7_44374119_44495658 | NUDCD3 | copy fasta | chr7 | 44374119 | 44495658 |
t0036 | 0/0 | 6951 | 1 | 0 | 0 | 1 | 0 | 0 | NUDCD3_chr7_44374119_44495658 | NUDCD3 | copy fasta | chr7 | 44374119 | 44495658 |
t0037 | 0/0 | 6951 | 1 | 0 | 0 | 0 | 0 | 1 | NUDCD3_chr7_44374119_44495658 | NUDCD3 | copy fasta | chr7 | 44374119 | 44495658 |
t0038 | 0/0 | 6951 | 1 | 1 | 0 | 0 | 0 | 0 | NUDCD3_chr7_44374119_44495658 | NUDCD3 | copy fasta | chr7 | 44374119 | 44495658 |
t0039 | 0/0 | 6951 | 1 | 0 | 0 | 1 | 0 | 0 | NUDCD3_chr7_44374119_44495658 | NUDCD3 | copy fasta | chr7 | 44374119 | 44495658 |
t0040 | 0/0 | 6951 | 1 | 1 | 0 | 0 | 0 | 0 | NUDCD3_chr7_44374119_44495658 | NUDCD3 | copy fasta | chr7 | 44374119 | 44495658 |
ghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
g0001 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
g0002 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
g0003 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
g0004 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
g0005 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
g0006 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
g0007 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
g0008 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
g0009 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
g0010 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
g0011 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
g0012 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
g0013 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
g0014 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
g0015 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
g0024 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
g0025 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
g0028 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
g0031 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
g0047 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
g0052 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
g0053 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
g0058 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
g0060 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
g0062 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
g0065 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
g0066 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
g0070 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
g0071 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
g0073 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
g0076 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
g0079 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
g0080 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
g0081 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
g0082 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
g0083 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
g0085 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
g0086 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
g0087 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
g0088 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
g0089 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
g0090 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
g0091 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
g0102 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
g0103 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
g0104 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
g0106 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
g0112 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
g0113 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
g0116 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
g0120 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
g0126 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
g0127 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
g0128 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
g0129 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
g0135 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
g0138 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
g0142 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
g0145 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
g0152 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
g0156 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
g0157 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
g0158 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
g0159 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
g0160 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
g0161 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
g0162 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
g0163 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
g0166 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
g0168 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
g0169 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
g0170 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
g0172 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
g0177 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
g0178 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
g0179 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
g0180 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
g0181 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
g0183 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
g0184 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
g0185 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
g0186 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
g0188 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
g0189 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
g0193 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
g0207 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
g0208 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
g0210 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
g0211 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
g0212 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
g0213 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
g0215 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
g0216 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
g0218 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
g0219 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
g0220 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
g0221 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
g0222 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
g0223 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
g0224 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
g0225 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
g0226 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
g0227 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
g0228 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
g0230 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
g0232 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
g0233 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
achapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 1/0 | 1086 | 188 | 41 | 37 | 69 | 10 | 30 | NUDCD3_chr7_44374119_44495658 | NUDCD3 | copy fasta | chr7 | 44374119 | 44495658 |
a0001c0006 | 0/0 | 1086 | 1 | 0 | 0 | 1 | 0 | 0 | NUDCD3_chr7_44374119_44495658 | NUDCD3 | copy fasta | chr7 | 44374119 | 44495658 |
a0002c0002 | 0/0 | 1086 | 26 | 17 | 6 | 0 | 0 | 3 | NUDCD3_chr7_44374119_44495658 | NUDCD3 | copy fasta | chr7 | 44374119 | 44495658 |
a0002c0005 | 0/0 | 1086 | 2 | 2 | 0 | 0 | 0 | 0 | NUDCD3_chr7_44374119_44495658 | NUDCD3 | copy fasta | chr7 | 44374119 | 44495658 |
a0003c0003 | 0/1 | 1086 | 17 | 0 | 4 | 3 | 4 | 5 | NUDCD3_chr7_44374119_44495658 | NUDCD3 | copy fasta | chr7 | 44374119 | 44495658 |
a0004c0004 | 0/0 | 1086 | 3 | 2 | 1 | 0 | 0 | 0 | NUDCD3_chr7_44374119_44495658 | NUDCD3 | copy fasta | chr7 | 44374119 | 44495658 |
a0005c0007 | 0/0 | 1086 | 1 | 0 | 0 | 1 | 0 | 0 | NUDCD3_chr7_44374119_44495658 | NUDCD3 | copy fasta | chr7 | 44374119 | 44495658 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 0/0 | 8036 | 128 | 34 | 23 | 47 | 5 | 19 | NUDCD3_chr7_44374119_44495658 | NUDCD3 | copy fasta | chr7 | 44374119 | 44495658 |
a0001c0001t0002 | 1/0 | 8036 | 25 | 0 | 4 | 9 | 4 | 7 | NUDCD3_chr7_44374119_44495658 | NUDCD3 | copy fasta | chr7 | 44374119 | 44495658 |
a0001c0001t0003 | 0/0 | 8037 | 10 | 0 | 1 | 8 | 1 | 0 | NUDCD3_chr7_44374119_44495658 | NUDCD3 | copy fasta | chr7 | 44374119 | 44495658 |
a0001c0001t0013 | 0/0 | 8036 | 2 | 2 | 0 | 0 | 0 | 0 | NUDCD3_chr7_44374119_44495658 | NUDCD3 | copy fasta | chr7 | 44374119 | 44495658 |
a0001c0001t0014 | 0/0 | 8037 | 2 | 0 | 1 | 0 | 0 | 1 | NUDCD3_chr7_44374119_44495658 | NUDCD3 | copy fasta | chr7 | 44374119 | 44495658 |
a0001c0001t0015 | 0/0 | 8036 | 2 | 0 | 2 | 0 | 0 | 0 | NUDCD3_chr7_44374119_44495658 | NUDCD3 | copy fasta | chr7 | 44374119 | 44495658 |
a0001c0001t0016 | 0/0 | 8036 | 2 | 0 | 2 | 0 | 0 | 0 | NUDCD3_chr7_44374119_44495658 | NUDCD3 | copy fasta | chr7 | 44374119 | 44495658 |
a0001c0001t0017 | 0/0 | 8036 | 2 | 2 | 0 | 0 | 0 | 0 | NUDCD3_chr7_44374119_44495658 | NUDCD3 | copy fasta | chr7 | 44374119 | 44495658 |
a0001c0001t0024 | 0/0 | 8036 | 1 | 0 | 0 | 0 | 0 | 1 | NUDCD3_chr7_44374119_44495658 | NUDCD3 | copy fasta | chr7 | 44374119 | 44495658 |
a0001c0001t0025 | 0/0 | 8036 | 1 | 0 | 0 | 0 | 0 | 1 | NUDCD3_chr7_44374119_44495658 | NUDCD3 | copy fasta | chr7 | 44374119 | 44495658 |
a0001c0001t0026 | 0/0 | 8036 | 1 | 0 | 1 | 0 | 0 | 0 | NUDCD3_chr7_44374119_44495658 | NUDCD3 | copy fasta | chr7 | 44374119 | 44495658 |
a0001c0001t0027 | 0/0 | 8036 | 1 | 1 | 0 | 0 | 0 | 0 | NUDCD3_chr7_44374119_44495658 | NUDCD3 | copy fasta | chr7 | 44374119 | 44495658 |
a0001c0001t0028 | 0/0 | 8037 | 1 | 0 | 0 | 1 | 0 | 0 | NUDCD3_chr7_44374119_44495658 | NUDCD3 | copy fasta | chr7 | 44374119 | 44495658 |
a0001c0001t0029 | 0/0 | 8036 | 1 | 1 | 0 | 0 | 0 | 0 | NUDCD3_chr7_44374119_44495658 | NUDCD3 | copy fasta | chr7 | 44374119 | 44495658 |
a0001c0001t0030 | 0/0 | 8036 | 1 | 0 | 1 | 0 | 0 | 0 | NUDCD3_chr7_44374119_44495658 | NUDCD3 | copy fasta | chr7 | 44374119 | 44495658 |
a0001c0001t0031 | 0/0 | 8036 | 1 | 0 | 1 | 0 | 0 | 0 | NUDCD3_chr7_44374119_44495658 | NUDCD3 | copy fasta | chr7 | 44374119 | 44495658 |
a0001c0001t0032 | 0/0 | 8036 | 1 | 0 | 1 | 0 | 0 | 0 | NUDCD3_chr7_44374119_44495658 | NUDCD3 | copy fasta | chr7 | 44374119 | 44495658 |
a0001c0001t0033 | 0/0 | 8036 | 1 | 1 | 0 | 0 | 0 | 0 | NUDCD3_chr7_44374119_44495658 | NUDCD3 | copy fasta | chr7 | 44374119 | 44495658 |
a0001c0001t0034 | 0/0 | 8037 | 1 | 0 | 0 | 1 | 0 | 0 | NUDCD3_chr7_44374119_44495658 | NUDCD3 | copy fasta | chr7 | 44374119 | 44495658 |
a0001c0001t0035 | 0/0 | 8036 | 1 | 0 | 0 | 1 | 0 | 0 | NUDCD3_chr7_44374119_44495658 | NUDCD3 | copy fasta | chr7 | 44374119 | 44495658 |
a0001c0001t0036 | 0/0 | 8036 | 1 | 0 | 0 | 1 | 0 | 0 | NUDCD3_chr7_44374119_44495658 | NUDCD3 | copy fasta | chr7 | 44374119 | 44495658 |
a0001c0001t0037 | 0/0 | 8036 | 1 | 0 | 0 | 0 | 0 | 1 | NUDCD3_chr7_44374119_44495658 | NUDCD3 | copy fasta | chr7 | 44374119 | 44495658 |
a0001c0001t0039 | 0/0 | 8036 | 1 | 0 | 0 | 1 | 0 | 0 | NUDCD3_chr7_44374119_44495658 | NUDCD3 | copy fasta | chr7 | 44374119 | 44495658 |
a0001c0006t0001 | 0/0 | 8036 | 1 | 0 | 0 | 1 | 0 | 0 | NUDCD3_chr7_44374119_44495658 | NUDCD3 | copy fasta | chr7 | 44374119 | 44495658 |
a0002c0002t0004 | 0/0 | 8036 | 8 | 1 | 4 | 0 | 0 | 3 | NUDCD3_chr7_44374119_44495658 | NUDCD3 | copy fasta | chr7 | 44374119 | 44495658 |
a0002c0002t0007 | 0/0 | 8034 | 3 | 3 | 0 | 0 | 0 | 0 | NUDCD3_chr7_44374119_44495658 | NUDCD3 | copy fasta | chr7 | 44374119 | 44495658 |
a0002c0002t0008 | 0/0 | 8034 | 3 | 3 | 0 | 0 | 0 | 0 | NUDCD3_chr7_44374119_44495658 | NUDCD3 | copy fasta | chr7 | 44374119 | 44495658 |
a0002c0002t0010 | 0/0 | 8034 | 2 | 1 | 1 | 0 | 0 | 0 | NUDCD3_chr7_44374119_44495658 | NUDCD3 | copy fasta | chr7 | 44374119 | 44495658 |
a0002c0002t0011 | 0/0 | 8034 | 2 | 2 | 0 | 0 | 0 | 0 | NUDCD3_chr7_44374119_44495658 | NUDCD3 | copy fasta | chr7 | 44374119 | 44495658 |
a0002c0002t0018 | 0/0 | 8036 | 2 | 2 | 0 | 0 | 0 | 0 | NUDCD3_chr7_44374119_44495658 | NUDCD3 | copy fasta | chr7 | 44374119 | 44495658 |
a0002c0002t0020 | 0/0 | 8036 | 1 | 1 | 0 | 0 | 0 | 0 | NUDCD3_chr7_44374119_44495658 | NUDCD3 | copy fasta | chr7 | 44374119 | 44495658 |
a0002c0002t0021 | 0/0 | 8036 | 1 | 1 | 0 | 0 | 0 | 0 | NUDCD3_chr7_44374119_44495658 | NUDCD3 | copy fasta | chr7 | 44374119 | 44495658 |
a0002c0002t0022 | 0/0 | 8036 | 1 | 0 | 1 | 0 | 0 | 0 | NUDCD3_chr7_44374119_44495658 | NUDCD3 | copy fasta | chr7 | 44374119 | 44495658 |
a0002c0002t0023 | 0/0 | 8036 | 1 | 1 | 0 | 0 | 0 | 0 | NUDCD3_chr7_44374119_44495658 | NUDCD3 | copy fasta | chr7 | 44374119 | 44495658 |
a0002c0002t0038 | 0/0 | 8036 | 1 | 1 | 0 | 0 | 0 | 0 | NUDCD3_chr7_44374119_44495658 | NUDCD3 | copy fasta | chr7 | 44374119 | 44495658 |
a0002c0002t0040 | 0/0 | 8036 | 1 | 1 | 0 | 0 | 0 | 0 | NUDCD3_chr7_44374119_44495658 | NUDCD3 | copy fasta | chr7 | 44374119 | 44495658 |
a0002c0005t0012 | 0/0 | 8037 | 2 | 2 | 0 | 0 | 0 | 0 | NUDCD3_chr7_44374119_44495658 | NUDCD3 | copy fasta | chr7 | 44374119 | 44495658 |
a0003c0003t0005 | 0/0 | 8036 | 8 | 0 | 3 | 0 | 3 | 2 | NUDCD3_chr7_44374119_44495658 | NUDCD3 | copy fasta | chr7 | 44374119 | 44495658 |
a0003c0003t0006 | 0/0 | 8036 | 4 | 0 | 0 | 3 | 0 | 1 | NUDCD3_chr7_44374119_44495658 | NUDCD3 | copy fasta | chr7 | 44374119 | 44495658 |
a0003c0003t0009 | 0/1 | 8036 | 3 | 0 | 1 | 0 | 0 | 1 | NUDCD3_chr7_44374119_44495658 | NUDCD3 | copy fasta | chr7 | 44374119 | 44495658 |
a0003c0003t0019 | 0/0 | 8036 | 2 | 0 | 0 | 0 | 1 | 1 | NUDCD3_chr7_44374119_44495658 | NUDCD3 | copy fasta | chr7 | 44374119 | 44495658 |
a0004c0004t0003 | 0/0 | 8037 | 3 | 2 | 1 | 0 | 0 | 0 | NUDCD3_chr7_44374119_44495658 | NUDCD3 | copy fasta | chr7 | 44374119 | 44495658 |
a0005c0007t0001 | 0/0 | 8036 | 1 | 0 | 0 | 1 | 0 | 0 | NUDCD3_chr7_44374119_44495658 | NUDCD3 | copy fasta | chr7 | 44374119 | 44495658 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0001 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
a0001c0001t0001g0005 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
a0001c0001t0001g0006 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
a0001c0001t0001g0007 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
a0001c0001t0001g0008 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
a0001c0001t0001g0010 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
a0001c0001t0001g0012 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
a0001c0001t0001g0014 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
a0001c0001t0001g0015 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
a0001c0001t0001g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
a0001c0001t0001g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
a0001c0001t0001g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
a0001c0001t0001g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
a0001c0001t0001g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
a0001c0001t0001g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
a0001c0001t0001g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
a0001c0001t0001g0024 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
a0001c0001t0001g0028 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
a0001c0001t0001g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
a0001c0001t0001g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
a0001c0001t0001g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
a0001c0001t0001g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
a0001c0001t0001g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
a0001c0001t0001g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
a0001c0001t0001g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
a0001c0001t0001g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
a0001c0001t0001g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
a0001c0001t0001g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
a0001c0001t0001g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
a0001c0001t0001g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
a0001c0001t0001g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
a0001c0001t0001g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
a0001c0001t0001g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
a0001c0001t0001g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
a0001c0001t0001g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
a0001c0001t0001g0062 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
a0001c0001t0001g0066 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
a0001c0001t0001g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
a0001c0001t0001g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
a0001c0001t0001g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
a0001c0001t0001g0080 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
a0001c0001t0001g0082 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
a0001c0001t0001g0083 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
a0001c0001t0001g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
a0001c0001t0001g0085 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
a0001c0001t0001g0086 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
a0001c0001t0001g0087 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
a0001c0001t0001g0088 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
a0001c0001t0001g0089 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
a0001c0001t0001g0090 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
a0001c0001t0001g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
a0001c0001t0001g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
a0001c0001t0001g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
a0001c0001t0001g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
a0001c0001t0001g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
a0001c0001t0001g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
a0001c0001t0001g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
a0001c0001t0001g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
a0001c0001t0001g0102 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
a0001c0001t0001g0104 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
a0001c0001t0001g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
a0001c0001t0001g0106 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
a0001c0001t0001g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
a0001c0001t0001g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
a0001c0001t0001g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
a0001c0001t0001g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
a0001c0001t0001g0112 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
a0001c0001t0001g0113 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
a0001c0001t0001g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
a0001c0001t0001g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
a0001c0001t0001g0116 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
a0001c0001t0001g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
a0001c0001t0001g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
a0001c0001t0001g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
a0001c0001t0001g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
a0001c0001t0001g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
a0001c0001t0001g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
a0001c0001t0001g0126 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
a0001c0001t0001g0127 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
a0001c0001t0001g0128 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
a0001c0001t0001g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
a0001c0001t0001g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
a0001c0001t0001g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
a0001c0001t0001g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
a0001c0001t0001g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
a0001c0001t0001g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
a0001c0001t0001g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
a0001c0001t0001g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
a0001c0001t0001g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
a0001c0001t0001g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
a0001c0001t0001g0142 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
a0001c0001t0001g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
a0001c0001t0001g0145 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
a0001c0001t0001g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
a0001c0001t0001g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
a0001c0001t0001g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
a0001c0001t0001g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
a0001c0001t0001g0152 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
a0001c0001t0001g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
a0001c0001t0001g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
a0001c0001t0001g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
a0001c0001t0001g0156 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
a0001c0001t0001g0157 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
a0001c0001t0001g0158 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
a0001c0001t0001g0159 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
a0001c0001t0001g0160 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
a0001c0001t0001g0161 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
a0001c0001t0001g0162 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
a0001c0001t0001g0163 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
a0001c0001t0001g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
a0001c0001t0001g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
a0001c0001t0001g0166 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
a0001c0001t0001g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
a0001c0001t0001g0168 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
a0001c0001t0001g0169 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
a0001c0001t0001g0170 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
a0001c0001t0001g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
a0001c0001t0001g0172 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
a0001c0001t0001g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
a0001c0001t0001g0177 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
a0001c0001t0001g0179 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
a0001c0001t0001g0181 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
a0001c0001t0001g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
a0001c0001t0001g0185 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
a0001c0001t0001g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
a0001c0001t0001g0188 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
a0001c0001t0001g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
a0001c0001t0002g0003 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
a0001c0001t0002g0011 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
a0001c0001t0002g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
a0001c0001t0002g0047 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
a0001c0001t0002g0052 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
a0001c0001t0002g0058 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
a0001c0001t0002g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
a0001c0001t0002g0060 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
a0001c0001t0002g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
a0001c0001t0002g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
a0001c0001t0002g0065 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
a0001c0001t0002g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
a0001c0001t0002g0070 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
a0001c0001t0002g0071 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
a0001c0001t0002g0073 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
a0001c0001t0002g0076 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
a0001c0001t0002g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
a0001c0001t0002g0091 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
a0001c0001t0002g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
a0001c0001t0002g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
a0001c0001t0002g0178 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
a0001c0001t0002g0183 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
a0001c0001t0002g0184 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
a0001c0001t0002g0189 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
a0001c0001t0002g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
a0001c0001t0003g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
a0001c0001t0003g0031 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
a0001c0001t0003g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
a0001c0001t0003g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
a0001c0001t0003g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
a0001c0001t0003g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
a0001c0001t0003g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
a0001c0001t0003g0135 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
a0001c0001t0003g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
a0001c0001t0003g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
a0001c0001t0013g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
a0001c0001t0013g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
a0001c0001t0014g0009 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
a0001c0001t0014g0013 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
a0001c0001t0015g0053 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
a0001c0001t0015g0079 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
a0001c0001t0016g0002 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
a0001c0001t0016g0004 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
a0001c0001t0017g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
a0001c0001t0017g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
a0001c0001t0024g0120 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
a0001c0001t0025g0129 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
a0001c0001t0026g0186 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
a0001c0001t0027g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
a0001c0001t0028g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
a0001c0001t0029g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
a0001c0001t0030g0180 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
a0001c0001t0031g0103 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
a0001c0001t0032g0138 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
a0001c0001t0033g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
a0001c0001t0034g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
a0001c0001t0035g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
a0001c0001t0036g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
a0001c0001t0037g0081 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
a0001c0001t0039g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
a0001c0006t0001g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
a0002c0002t0004g0207 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
a0002c0002t0004g0208 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
a0002c0002t0004g0210 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
a0002c0002t0004g0211 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
a0002c0002t0004g0212 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
a0002c0002t0004g0213 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
a0002c0002t0004g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
a0002c0002t0004g0216 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
a0002c0002t0007g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
a0002c0002t0007g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
a0002c0002t0007g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
a0002c0002t0008g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
a0002c0002t0008g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
a0002c0002t0008g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
a0002c0002t0010g0193 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
a0002c0002t0010g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
a0002c0002t0011g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
a0002c0002t0011g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
a0002c0002t0018g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
a0002c0002t0018g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
a0002c0002t0020g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
a0002c0002t0021g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
a0002c0002t0022g0215 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
a0002c0002t0023g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
a0002c0002t0038g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
a0002c0002t0040g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
a0002c0005t0012g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
a0002c0005t0012g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
a0003c0003t0005g0218 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
a0003c0003t0005g0219 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
a0003c0003t0005g0221 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
a0003c0003t0005g0222 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
a0003c0003t0005g0223 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
a0003c0003t0005g0224 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
a0003c0003t0005g0225 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
a0003c0003t0005g0233 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
a0003c0003t0006g0226 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
a0003c0003t0006g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
a0003c0003t0006g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
a0003c0003t0006g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
a0003c0003t0009g0220 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
a0003c0003t0009g0227 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
a0003c0003t0009g0228 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
a0003c0003t0019g0230 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
a0003c0003t0019g0232 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
a0004c0004t0003g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
a0004c0004t0003g0025 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
a0004c0004t0003g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
a0005c0007t0001g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0001 | c0001 | t0001 | g0090 | EUR | GBR | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
HG00099 | hp2 | a0003 | c0003 | t0005 | g0221 | EUR | GBR | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
HG00280 | hp1 | a0003 | c0003 | t0005 | g0233 | EUR | FIN | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
HG00280 | hp2 | a0003 | c0003 | t0019 | g0230 | EUR | FIN | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
HG00323 | hp1 | a0001 | c0001 | t0002 | g0052 | EUR | FIN | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
HG00323 | hp2 | a0001 | c0001 | t0003 | g0135 | EUR | FIN | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
HG00438 | hp1 | a0003 | c0003 | t0006 | g0234 | EAS | CHS | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
HG00438 | hp2 | a0001 | c0001 | t0001 | g0130 | EAS | CHS | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
HG00544 | hp1 | a0001 | c0001 | t0002 | g0078 | EAS | CHS | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
HG00544 | hp2 | a0001 | c0001 | t0001 | g0015 | EAS | CHS | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
HG00558 | hp1 | a0001 | c0001 | t0001 | g0115 | EAS | CHS | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
HG00558 | hp2 | a0001 | c0001 | t0002 | g0064 | EAS | CHS | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
HG00609 | hp1 | a0001 | c0001 | t0001 | g0165 | EAS | CHS | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
HG00609 | hp2 | a0005 | c0007 | t0001 | g0192 | EAS | CHS | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
HG00639 | hp1 | a0004 | c0004 | t0003 | g0025 | AMR | PUR | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
HG00639 | hp2 | a0001 | c0001 | t0002 | g0184 | AMR | PUR | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
HG00642 | hp1 | a0001 | c0001 | t0016 | g0002 | AMR | PUR | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
HG00642 | hp2 | a0001 | c0001 | t0001 | g0128 | AMR | PUR | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
HG00673 | hp1 | a0001 | c0001 | t0001 | g0077 | EAS | CHS | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
HG00673 | hp2 | a0001 | c0001 | t0002 | g0099 | EAS | CHS | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
HG00735 | hp1 | a0001 | c0001 | t0001 | g0085 | AMR | PUR | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
HG00735 | hp2 | a0002 | c0002 | t0004 | g0212 | AMR | PUR | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
HG00741 | hp1 | a0001 | c0001 | t0001 | g0172 | AMR | PUR | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
HG00741 | hp2 | a0002 | c0002 | t0010 | g0193 | AMR | PUR | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
HG01070 | hp1 | a0001 | c0001 | t0001 | g0113 | AMR | PUR | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
HG01070 | hp2 | a0002 | c0002 | t0004 | g0216 | AMR | PUR | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
HG01071 | hp1 | a0002 | c0002 | t0004 | g0213 | AMR | PUR | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
HG01071 | hp2 | a0001 | c0001 | t0001 | g0161 | AMR | PUR | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
HG01081 | hp1 | a0001 | c0001 | t0001 | g0106 | AMR | PUR | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
HG01081 | hp2 | a0001 | c0001 | t0002 | g0183 | AMR | PUR | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
HG01106 | hp1 | a0002 | c0002 | t0004 | g0210 | AMR | PUR | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
HG01106 | hp2 | a0001 | c0001 | t0001 | g0145 | AMR | PUR | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
HG01109 | hp1 | a0001 | c0001 | t0032 | g0138 | AMR | PUR | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
HG01109 | hp2 | a0002 | c0002 | t0022 | g0215 | AMR | PUR | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
HG01168 | hp1 | a0001 | c0001 | t0001 | g0169 | AMR | PUR | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
HG01168 | hp2 | a0003 | c0003 | t0005 | g0225 | AMR | PUR | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
HG01169 | hp1 | a0001 | c0001 | t0001 | g0170 | AMR | PUR | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
HG01169 | hp2 | a0001 | c0001 | t0001 | g0126 | AMR | PUR | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
HG01175 | hp1 | a0001 | c0001 | t0016 | g0004 | AMR | PUR | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
HG01175 | hp2 | a0001 | c0001 | t0001 | g0080 | AMR | PUR | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
HG01256 | hp1 | a0003 | c0003 | t0005 | g0222 | AMR | CLM | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
HG01256 | hp2 | a0001 | c0001 | t0001 | g0163 | AMR | CLM | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
HG01257 | hp1 | a0001 | c0001 | t0001 | g0177 | AMR | CLM | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
HG01257 | hp2 | a0001 | c0001 | t0015 | g0079 | AMR | CLM | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
HG01258 | hp1 | a0001 | c0001 | t0015 | g0053 | AMR | CLM | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
HG01258 | hp2 | a0003 | c0003 | t0005 | g0223 | AMR | CLM | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
HG01358 | hp1 | a0001 | c0001 | t0002 | g0076 | AMR | CLM | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
HG01358 | hp2 | a0003 | c0003 | t0009 | g0228 | AMR | CLM | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
HG01496 | hp1 | a0001 | c0001 | t0001 | g0181 | AMR | CLM | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
HG01496 | hp2 | a0001 | c0001 | t0030 | g0180 | AMR | CLM | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
HG01515 | hp1 | a0001 | c0001 | t0001 | g0066 | EUR | IBS | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
HG01515 | hp2 | a0001 | c0001 | t0002 | g0091 | EUR | IBS | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
HG01516 | hp1 | a0001 | c0001 | t0001 | g0168 | EUR | IBS | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
HG01516 | hp2 | a0001 | c0001 | t0001 | g0001 | EUR | IBS | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
HG01517 | hp1 | a0001 | c0001 | t0002 | g0065 | EUR | IBS | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
HG01517 | hp2 | a0001 | c0001 | t0001 | g0001 | EUR | IBS | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
HG01928 | hp1 | a0001 | c0001 | t0014 | g0013 | AMR | PEL | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
HG01928 | hp2 | a0001 | c0001 | t0001 | g0084 | AMR | PEL | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
HG01943 | hp1 | a0001 | c0001 | t0001 | g0101 | AMR | PEL | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
HG01943 | hp2 | a0001 | c0001 | t0001 | g0188 | AMR | PEL | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
HG01952 | hp1 | a0001 | c0001 | t0001 | g0024 | AMR | PEL | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
HG01952 | hp2 | a0001 | c0001 | t0001 | g0104 | AMR | PEL | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
HG01978 | hp1 | a0001 | c0001 | t0001 | g0112 | AMR | PEL | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
HG01978 | hp2 | a0001 | c0001 | t0026 | g0186 | AMR | PEL | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
HG01981 | hp1 | a0001 | c0001 | t0031 | g0103 | AMR | PEL | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
HG01981 | hp2 | a0001 | c0001 | t0002 | g0047 | AMR | PEL | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
HG01993 | hp1 | a0001 | c0001 | t0001 | g0102 | AMR | PEL | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
HG01993 | hp2 | a0001 | c0001 | t0001 | g0028 | AMR | PEL | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
HG02015 | hp1 | a0001 | c0001 | t0001 | g0167 | EAS | KHV | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
HG02015 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | KHV | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
HG02056 | hp1 | a0001 | c0001 | t0002 | g0122 | EAS | KHV | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
HG02056 | hp2 | a0001 | c0001 | t0001 | g0141 | EAS | KHV | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
HG02071 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | KHV | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
HG02071 | hp2 | a0001 | c0001 | t0002 | g0059 | EAS | KHV | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
HG02145 | hp1 | a0001 | c0001 | t0001 | g0045 | AFR | ACB | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
HG02145 | hp2 | a0001 | c0001 | t0001 | g0050 | AFR | ACB | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
HG02155 | hp1 | a0001 | c0001 | t0001 | g0150 | EAS | CDX | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
HG02155 | hp2 | a0001 | c0001 | t0001 | g0014 | EAS | CDX | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
HG02165 | hp1 | a0001 | c0001 | t0003 | g0033 | EAS | CDX | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
HG02165 | hp2 | a0001 | c0001 | t0001 | g0133 | EAS | CDX | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
HG02257 | hp1 | a0002 | c0002 | t0008 | g0204 | AFR | ACB | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
HG02257 | hp2 | a0001 | c0001 | t0001 | g0056 | AFR | ACB | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
HG02280 | hp1 | a0001 | c0001 | t0001 | g0019 | AFR | ACB | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
HG02280 | hp2 | a0002 | c0002 | t0038 | g0202 | AFR | ACB | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
HG02293 | hp1 | a0001 | c0001 | t0003 | g0031 | AMR | PEL | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
HG02293 | hp2 | a0001 | c0001 | t0001 | g0160 | AMR | PEL | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
HG02523 | hp1 | a0001 | c0001 | t0003 | g0043 | EAS | KHV | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
HG02523 | hp2 | a0001 | c0001 | t0002 | g0061 | EAS | KHV | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
HG02572 | hp1 | a0001 | c0001 | t0001 | g0036 | AFR | GWD | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
HG02572 | hp2 | a0001 | c0001 | t0001 | g0136 | AFR | GWD | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
HG02602 | hp1 | a0001 | c0001 | t0001 | g0152 | SAS | PJL | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
HG02602 | hp2 | a0001 | c0001 | t0002 | g0178 | SAS | PJL | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
HG02615 | hp1 | a0001 | c0001 | t0001 | g0018 | AFR | GWD | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
HG02615 | hp2 | a0001 | c0001 | t0001 | g0139 | AFR | GWD | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
HG02622 | hp1 | a0002 | c0002 | t0011 | g0194 | AFR | GWD | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
HG02622 | hp2 | a0001 | c0001 | t0013 | g0072 | AFR | GWD | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
HG02683 | hp1 | a0001 | c0001 | t0001 | g0086 | SAS | PJL | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
HG02683 | hp2 | a0002 | c0002 | t0004 | g0207 | SAS | PJL | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
HG02698 | hp1 | a0001 | c0001 | t0001 | g0088 | SAS | PJL | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
HG02698 | hp2 | a0001 | c0001 | t0002 | g0070 | SAS | PJL | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
HG02723 | hp1 | a0001 | c0001 | t0001 | g0117 | AFR | GWD | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
HG02723 | hp2 | a0001 | c0001 | t0027 | g0146 | AFR | GWD | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
HG02738 | hp1 | a0003 | c0003 | t0019 | g0232 | SAS | PJL | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
HG02738 | hp2 | a0001 | c0001 | t0001 | g0179 | SAS | PJL | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
HG02809 | hp1 | a0001 | c0001 | t0013 | g0123 | AFR | GWD | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
HG02809 | hp2 | a0001 | c0001 | t0001 | g0132 | AFR | GWD | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
HG02895 | hp1 | a0002 | c0002 | t0018 | g0199 | AFR | GWD | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
HG02895 | hp2 | a0001 | c0001 | t0001 | g0017 | AFR | GWD | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
HG02922 | hp1 | a0001 | c0001 | t0001 | g0048 | AFR | ESN | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
HG02922 | hp2 | a0002 | c0005 | t0012 | g0236 | AFR | ESN | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
HG02976 | hp1 | a0001 | c0001 | t0001 | g0054 | AFR | ESN | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
HG02976 | hp2 | a0002 | c0002 | t0004 | g0214 | AFR | ESN | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
HG03017 | hp1 | a0001 | c0001 | t0001 | g0062 | SAS | PJL | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
HG03017 | hp2 | a0001 | c0001 | t0002 | g0189 | SAS | PJL | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
HG03041 | hp1 | a0001 | c0001 | t0001 | g0134 | AFR | GWD | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
HG03041 | hp2 | a0001 | c0001 | t0001 | g0118 | AFR | GWD | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
HG03130 | hp1 | a0002 | c0002 | t0023 | g0209 | AFR | ESN | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
HG03130 | hp2 | a0001 | c0001 | t0001 | g0100 | AFR | ESN | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
HG03139 | hp1 | a0002 | c0002 | t0010 | g0201 | AFR | ESN | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
HG03139 | hp2 | a0001 | c0001 | t0001 | g0039 | AFR | ESN | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
HG03195 | hp1 | a0001 | c0001 | t0001 | g0137 | AFR | ESN | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
HG03195 | hp2 | a0001 | c0001 | t0001 | g0051 | AFR | ESN | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
HG03209 | hp1 | a0001 | c0001 | t0001 | g0140 | AFR | MSL | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
HG03209 | hp2 | a0001 | c0001 | t0001 | g0057 | AFR | MSL | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
HG03225 | hp1 | a0004 | c0004 | t0003 | g0016 | AFR | MSL | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
HG03225 | hp2 | a0001 | c0001 | t0001 | g0020 | AFR | MSL | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
HG03239 | hp1 | a0001 | c0001 | t0002 | g0073 | SAS | PJL | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
HG03239 | hp2 | a0001 | c0001 | t0001 | g0087 | SAS | PJL | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
HG03453 | hp1 | a0002 | c0002 | t0007 | g0197 | AFR | MSL | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
HG03453 | hp2 | a0001 | c0001 | t0033 | g0173 | AFR | MSL | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
HG03486 | hp1 | a0002 | c0002 | t0021 | g0217 | AFR | MSL | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
HG03486 | hp2 | a0001 | c0001 | t0017 | g0068 | AFR | MSL | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
HG03491 | hp1 | a0003 | c0003 | t0005 | g0219 | SAS | PJL | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
HG03491 | hp2 | a0001 | c0001 | t0002 | g0011 | SAS | PJL | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
HG03492 | hp1 | a0001 | c0001 | t0002 | g0071 | SAS | PJL | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
HG03492 | hp2 | a0003 | c0003 | t0005 | g0218 | SAS | PJL | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
HG03516 | hp1 | a0002 | c0002 | t0007 | g0196 | AFR | ESN | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
HG03516 | hp2 | a0001 | c0001 | t0001 | g0094 | AFR | ESN | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
HG03579 | hp1 | a0002 | c0005 | t0012 | g0235 | AFR | MSL | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
HG03579 | hp2 | a0001 | c0001 | t0001 | g0174 | AFR | MSL | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
HG03654 | hp1 | a0002 | c0002 | t0004 | g0211 | SAS | PJL | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
HG03654 | hp2 | a0001 | c0001 | t0001 | g0127 | SAS | PJL | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
HG03710 | hp1 | a0001 | c0001 | t0001 | g0089 | SAS | PJL | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
HG03710 | hp2 | a0001 | c0001 | t0001 | g0157 | SAS | PJL | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
HG03831 | hp1 | a0001 | c0001 | t0024 | g0120 | SAS | BEB | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
HG03831 | hp2 | a0001 | c0001 | t0025 | g0129 | SAS | BEB | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
HG03834 | hp1 | a0001 | c0001 | t0001 | g0156 | SAS | BEB | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
HG03834 | hp2 | a0001 | c0001 | t0001 | g0082 | SAS | BEB | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
HG03927 | hp1 | a0001 | c0001 | t0001 | g0116 | SAS | BEB | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
HG03927 | hp2 | a0001 | c0001 | t0001 | g0166 | SAS | BEB | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
HG03942 | hp1 | a0002 | c0002 | t0004 | g0208 | SAS | BEB | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
HG03942 | hp2 | a0001 | c0001 | t0001 | g0083 | SAS | BEB | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
HG04115 | hp1 | a0001 | c0001 | t0001 | g0185 | SAS | STU | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
HG04115 | hp2 | a0001 | c0001 | t0002 | g0058 | SAS | STU | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
HG04184 | hp1 | a0001 | c0001 | t0001 | g0142 | SAS | BEB | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
HG04184 | hp2 | a0003 | c0003 | t0009 | g0220 | SAS | BEB | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
HG04199 | hp1 | a0001 | c0001 | t0001 | g0162 | SAS | STU | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
HG04199 | hp2 | a0001 | c0001 | t0014 | g0009 | SAS | STU | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
HG04204 | hp1 | a0003 | c0003 | t0006 | g0226 | SAS | STU | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
HG04204 | hp2 | a0001 | c0001 | t0001 | g0159 | SAS | STU | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
NA18522 | hp1 | a0004 | c0004 | t0003 | g0026 | AFR | YRI | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
NA18522 | hp2 | a0002 | c0002 | t0008 | g0206 | AFR | YRI | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
NA18612 | hp1 | a0001 | c0001 | t0001 | g0155 | EAS | CHB | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
NA18612 | hp2 | a0001 | c0001 | t0001 | g0040 | EAS | CHB | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
NA18941 | hp1 | a0001 | c0001 | t0034 | g0029 | EAS | JPT | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
NA18941 | hp2 | a0001 | c0001 | t0001 | g0023 | EAS | JPT | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
NA18948 | hp1 | a0001 | c0001 | t0001 | g0154 | EAS | JPT | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
NA18948 | hp2 | a0001 | c0001 | t0001 | g0034 | EAS | JPT | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
NA18957 | hp1 | a0001 | c0001 | t0001 | g0110 | EAS | JPT | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
NA18957 | hp2 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
NA18960 | hp1 | a0001 | c0001 | t0001 | g0098 | EAS | JPT | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
NA18960 | hp2 | a0001 | c0001 | t0001 | g0143 | EAS | JPT | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
NA18965 | hp1 | a0001 | c0006 | t0001 | g0149 | EAS | JPT | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
NA18965 | hp2 | a0001 | c0001 | t0001 | g0108 | EAS | JPT | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
NA18970 | hp1 | a0001 | c0001 | t0039 | g0092 | EAS | JPT | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
NA18970 | hp2 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
NA18971 | hp1 | a0001 | c0001 | t0001 | g0151 | EAS | JPT | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
NA18971 | hp2 | a0001 | c0001 | t0003 | g0032 | EAS | JPT | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
NA18974 | hp1 | a0001 | c0001 | t0003 | g0175 | EAS | JPT | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
NA18974 | hp2 | a0001 | c0001 | t0001 | g0093 | EAS | JPT | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
NA18975 | hp1 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
NA18975 | hp2 | a0001 | c0001 | t0001 | g0153 | EAS | JPT | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
NA18979 | hp1 | a0001 | c0001 | t0001 | g0164 | EAS | JPT | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
NA18979 | hp2 | a0003 | c0003 | t0006 | g0231 | EAS | JPT | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
NA18981 | hp1 | a0001 | c0001 | t0036 | g0144 | EAS | JPT | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
NA18981 | hp2 | a0001 | c0001 | t0001 | g0109 | EAS | JPT | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
NA18983 | hp1 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
NA18983 | hp2 | a0001 | c0001 | t0003 | g0030 | EAS | JPT | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
NA18985 | hp1 | a0001 | c0001 | t0001 | g0191 | EAS | JPT | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
NA18985 | hp2 | a0001 | c0001 | t0001 | g0107 | EAS | JPT | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
NA18989 | hp1 | a0001 | c0001 | t0001 | g0182 | EAS | JPT | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
NA18989 | hp2 | a0001 | c0001 | t0001 | g0049 | EAS | JPT | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
NA19003 | hp1 | a0001 | c0001 | t0003 | g0176 | EAS | JPT | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
NA19003 | hp2 | a0001 | c0001 | t0001 | g0022 | EAS | JPT | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
NA19005 | hp1 | a0001 | c0001 | t0035 | g0027 | EAS | JPT | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
NA19005 | hp2 | a0001 | c0001 | t0001 | g0046 | EAS | JPT | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
NA19007 | hp1 | a0001 | c0001 | t0001 | g0105 | EAS | JPT | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
NA19007 | hp2 | a0001 | c0001 | t0002 | g0067 | EAS | JPT | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
NA19030 | hp1 | a0001 | c0001 | t0001 | g0095 | AFR | LWK | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
NA19030 | hp2 | a0001 | c0001 | t0001 | g0075 | AFR | LWK | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
NA19043 | hp1 | a0002 | c0002 | t0007 | g0198 | AFR | LWK | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
NA19043 | hp2 | a0001 | c0001 | t0001 | g0074 | AFR | LWK | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
NA19060 | hp1 | a0001 | c0001 | t0001 | g0125 | EAS | JPT | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
NA19060 | hp2 | a0001 | c0001 | t0001 | g0096 | EAS | JPT | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
NA19062 | hp1 | a0001 | c0001 | t0003 | g0044 | EAS | JPT | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
NA19062 | hp2 | a0001 | c0001 | t0001 | g0041 | EAS | JPT | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
NA19063 | hp1 | a0001 | c0001 | t0001 | g0171 | EAS | JPT | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
NA19063 | hp2 | a0001 | c0001 | t0028 | g0111 | EAS | JPT | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
NA19065 | hp1 | a0001 | c0001 | t0002 | g0190 | EAS | JPT | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
NA19065 | hp2 | a0003 | c0003 | t0006 | g0229 | EAS | JPT | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
NA19074 | hp1 | a0001 | c0001 | t0001 | g0147 | EAS | JPT | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
NA19074 | hp2 | a0001 | c0001 | t0001 | g0114 | EAS | JPT | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
NA19077 | hp1 | a0001 | c0001 | t0001 | g0021 | EAS | JPT | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
NA19077 | hp2 | a0001 | c0001 | t0001 | g0124 | EAS | JPT | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
NA19084 | hp1 | a0001 | c0001 | t0002 | g0042 | EAS | JPT | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
NA19084 | hp2 | a0001 | c0001 | t0003 | g0063 | EAS | JPT | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
NA20805 | hp1 | a0001 | c0001 | t0002 | g0060 | EUR | TSI | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
NA20805 | hp2 | a0003 | c0003 | t0005 | g0224 | EUR | TSI | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
NA20905 | hp1 | a0001 | c0001 | t0001 | g0158 | SAS | GIH | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
NA20905 | hp2 | a0001 | c0001 | t0037 | g0081 | SAS | GIH | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
HG02109 | hp1 | a0001 | c0001 | t0001 | g0038 | AFR | ACB | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
HG02109 | hp2 | a0001 | c0001 | t0017 | g0069 | AFR | ACB | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
HG02486 | hp1 | a0001 | c0001 | t0001 | g0037 | AFR | ACB | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
HG02486 | hp2 | a0002 | c0002 | t0011 | g0195 | AFR | ACB | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
HG02559 | hp1 | a0001 | c0001 | t0001 | g0121 | AFR | ACB | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
HG02559 | hp2 | a0001 | c0001 | t0029 | g0055 | AFR | ACB | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
HG03471 | hp1 | a0001 | c0001 | t0001 | g0131 | AFR | MSL | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
HG03471 | hp2 | a0001 | c0001 | t0001 | g0119 | AFR | MSL | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
HG06807 | hp1 | a0001 | c0001 | t0001 | g0035 | AFR | USA | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
HG06807 | hp2 | a0002 | c0002 | t0018 | g0200 | AFR | USA | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
NA18955 | hp1 | a0001 | c0001 | t0001 | g0097 | EAS | JPT | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
NA18955 | hp2 | a0001 | c0001 | t0001 | g0148 | EAS | JPT | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
NA20300 | hp1 | a0002 | c0002 | t0020 | g0203 | AFR | USA | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
NA20300 | hp2 | a0001 | c0001 | t0001 | g0187 | AFR | USA | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
NA21309 | hp1 | a0002 | c0002 | t0040 | g0237 | AFR | LWK | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
NA21309 | hp2 | a0002 | c0002 | t0008 | g0205 | AFR | LWK | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
homoSapiens_chm13v2 | hp1 | a0003 | c0003 | t0009 | g0227 | REF | REF | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
homoSapiens_grch38 | hp1 | a0001 | c0001 | t0002 | g0003 | REF | REF | NUDCD3_chr7_44374119_44495658 | NUDCD3 | chr7 | 44374119 | 44495658 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr7:44404523
|
G | A | 1 | a0003 | 17 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(14): Show |
missense_variant | MODERATE | c.703C>T | p.Arg235Cys | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 4/6 | 761/8036 | 703/1086 | 235/361 | chr7 | 44404523 | ||
chr7:44485109
|
T | A | 1 | a0004 | 3 | HG00639.hp1 HG03225.hp1 NA18522.hp1 |
missense_variant | MODERATE | c.368A>T | p.Glu123Val | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 2/6 | 426/8036 | 368/1086 | 123/361 | chr7 | 44485109 | ||
chr7:44485110
|
C | T | 1 | a0004 | 3 | HG00639.hp1 HG03225.hp1 NA18522.hp1 |
missense_variant | MODERATE | c.367G>A | p.Glu123Lys | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 2/6 | 425/8036 | 367/1086 | 123/361 | chr7 | 44485110 | ||
chr7:44490587
|
G | A | 1 | a0005 | 1 | HG00609.hp2 | missense_variant | MODERATE | c.14C>T | p.Ala5Val | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 1/6 | 72/8036 | 14/1086 | 5/361 | chr7 | 44490587 | ||
chr7:44490594
|
T | G | 2 | a0002a0003 | 45 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(42): Show |
missense_variant | MODERATE | c.7A>C | p.Thr3Pro | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 1/6 | 65/8036 | 7/1086 | 3/361 | chr7 | 44490594 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr7:44392359
|
A | G | 1 | a0001c0006 | 1 | NA18965.hp1 | synonymous_variant | LOW | c.913T>C | p.Leu305Leu | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 5/6 | 971/8036 | 913/1086 | 305/361 | chr7 | 44392359 | ||
chr7:44485075
|
C | T | 1 | a0002c0005 | 2 | HG02922.hp2 HG03579.hp1 |
synonymous_variant | LOW | c.402G>A | p.Gln134Gln | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 2/6 | 460/8036 | 402/1086 | 134/361 | chr7 | 44485075 | ||
chr7:44490499
|
G | A | 1 | a0002c0005 | 2 | HG02922.hp2 HG03579.hp1 |
synonymous_variant | LOW | c.102C>T | p.Leu34Leu | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 1/6 | 160/8036 | 102/1086 | 34/361 | chr7 | 44490499 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr7:44379125
|
T | A | 1 | a0002c0002t0018 | 2 | HG02895.hp1 HG06807.hp2 |
3_prime_UTR_variant | MODIFIER | c.*6886A>T | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 6/6 | 6886 | chr7 | 44379125 | |||||
chr7:44379147
|
G | A | 1 | a0001c0001t0027 | 1 | HG02723.hp2 | 3_prime_UTR_variant | MODIFIER | c.*6864C>T | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 6/6 | 6864 | chr7 | 44379147 | |||||
chr7:44379287
|
C | CA | 3 | a0001c0001t0014a0001c0001t0028a0002c0005t0012 | 5 | HG01928.hp1 HG02922.hp2 HG03579.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*6723dupT | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 6/6 | 6723 | chr7 | 44379287 | |||||
chr7:44379293
|
A | G | 1 | a0002c0002t0021 | 1 | HG03486.hp1 | 3_prime_UTR_variant | MODIFIER | c.*6718T>C | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 6/6 | 6718 | chr7 | 44379293 | |||||
chr7:44379382
|
G | A | 1 | a0001c0001t0029 | 1 | HG02559.hp2 | 3_prime_UTR_variant | MODIFIER | c.*6629C>T | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 6/6 | 6629 | chr7 | 44379382 | |||||
chr7:44379569
|
A | G | 10 | a0002c0002t0007a0002c0002t0010a0002c0002t0011others(7): Show | 26 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(23): Show |
3_prime_UTR_variant | MODIFIER | c.*6442T>C | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 6/6 | 6442 | chr7 | 44379569 | |||||
chr7:44379592
|
C | T | 3 | a0003c0003t0005a0003c0003t0006a0003c0003t0019 | 14 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(11): Show |
3_prime_UTR_variant | MODIFIER | c.*6419G>A | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 6/6 | 6419 | chr7 | 44379592 | |||||
chr7:44379886
|
G | A | 1 | a0001c0001t0034 | 1 | NA18941.hp1 | 3_prime_UTR_variant | MODIFIER | c.*6125C>T | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 6/6 | 6125 | chr7 | 44379886 | |||||
chr7:44380008
|
G | A | 1 | a0002c0002t0011 | 2 | HG02486.hp2 HG02622.hp1 |
3_prime_UTR_variant | MODIFIER | c.*6003C>T | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 6/6 | 6003 | chr7 | 44380008 | |||||
chr7:44380074
|
T | A | 2 | a0002c0002t0004a0002c0002t0022 | 9 | HG00735.hp2 HG01070.hp2 HG01071.hp1 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*5937A>T | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 6/6 | 5937 | chr7 | 44380074 | |||||
chr7:44380102
|
C | T | 4 | a0002c0002t0004a0002c0002t0020a0002c0002t0022others(1): Show | 11 | HG00735.hp2 HG01070.hp2 HG01071.hp1 others(8): Show |
3_prime_UTR_variant | MODIFIER | c.*5909G>A | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 6/6 | 5909 | chr7 | 44380102 | |||||
chr7:44380129
|
G | T | 1 | a0002c0002t0008 | 3 | HG02257.hp1 NA18522.hp2 NA21309.hp2 |
3_prime_UTR_variant | MODIFIER | c.*5882C>A | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 6/6 | 5882 | chr7 | 44380129 | |||||
chr7:44380336
|
G | C | 1 | a0002c0002t0007 | 3 | HG03453.hp1 HG03516.hp1 NA19043.hp1 |
3_prime_UTR_variant | MODIFIER | c.*5675C>G | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 6/6 | 5675 | chr7 | 44380336 | |||||
chr7:44380548
|
G | C | 8 | a0002c0002t0007a0002c0002t0010a0002c0002t0011others(5): Show | 23 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(20): Show |
3_prime_UTR_variant | MODIFIER | c.*5463C>G | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 6/6 | 5463 | chr7 | 44380548 | |||||
chr7:44380572
|
G | A | 1 | a0003c0003t0019 | 2 | HG00280.hp2 HG02738.hp1 |
3_prime_UTR_variant | MODIFIER | c.*5439C>T | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 6/6 | 5439 | chr7 | 44380572 | |||||
chr7:44380573
|
C | T | 2 | a0002c0002t0021a0002c0002t0040 | 2 | HG03486.hp1 NA21309.hp1 |
3_prime_UTR_variant | MODIFIER | c.*5438G>A | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 6/6 | 5438 | chr7 | 44380573 | |||||
chr7:44380639
|
A | G | 8 | a0002c0002t0007a0002c0002t0010a0002c0002t0011others(5): Show | 23 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(20): Show |
3_prime_UTR_variant | MODIFIER | c.*5372T>C | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 6/6 | 5372 | chr7 | 44380639 | |||||
chr7:44380725
|
G | A | 1 | a0001c0001t0030 | 1 | HG01496.hp2 | 3_prime_UTR_variant | MODIFIER | c.*5286C>T | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 6/6 | 5286 | chr7 | 44380725 | |||||
chr7:44380763
|
A | G | 5 | a0002c0002t0021a0002c0002t0040a0003c0003t0005others(2): Show | 16 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(13): Show |
3_prime_UTR_variant | MODIFIER | c.*5248T>C | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 6/6 | 5248 | chr7 | 44380763 | |||||
chr7:44380859
|
A | C | 1 | a0002c0002t0022 | 1 | HG01109.hp2 | 3_prime_UTR_variant | MODIFIER | c.*5152T>G | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 6/6 | 5152 | chr7 | 44380859 | |||||
chr7:44381040
|
C | A | 3 | a0003c0003t0005a0003c0003t0006a0003c0003t0019 | 14 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(11): Show |
3_prime_UTR_variant | MODIFIER | c.*4971G>T | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 6/6 | 4971 | chr7 | 44381040 | |||||
chr7:44381051
|
C | T | 2 | a0002c0002t0021a0002c0002t0040 | 2 | HG03486.hp1 NA21309.hp1 |
3_prime_UTR_variant | MODIFIER | c.*4960G>A | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 6/6 | 4960 | chr7 | 44381051 | |||||
chr7:44381052
|
A | G | 3 | a0003c0003t0005a0003c0003t0006a0003c0003t0019 | 14 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(11): Show |
3_prime_UTR_variant | MODIFIER | c.*4959T>C | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 6/6 | 4959 | chr7 | 44381052 | |||||
chr7:44381155
|
C | T | 36 | a0001c0001t0001a0001c0001t0003a0001c0001t0013others(33): Show | 202 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(199): Show |
3_prime_UTR_variant | MODIFIER | c.*4856G>A | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 6/6 | 4856 | chr7 | 44381155 | |||||
chr7:44381302
|
A | G | 2 | a0003c0003t0006a0003c0003t0019 | 6 | HG00280.hp2 HG00438.hp1 HG02738.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*4709T>C | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 6/6 | 4709 | chr7 | 44381302 | |||||
chr7:44381489
|
C | T | 1 | a0002c0005t0012 | 2 | HG02922.hp2 HG03579.hp1 |
3_prime_UTR_variant | MODIFIER | c.*4522G>A | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 6/6 | 4522 | chr7 | 44381489 | |||||
chr7:44381524
|
T | C | 1 | a0001c0001t0031 | 1 | HG01981.hp1 | 3_prime_UTR_variant | MODIFIER | c.*4487A>G | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 6/6 | 4487 | chr7 | 44381524 | |||||
chr7:44381793
|
C | T | 1 | a0003c0003t0019 | 2 | HG00280.hp2 HG02738.hp1 |
3_prime_UTR_variant | MODIFIER | c.*4218G>A | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 6/6 | 4218 | chr7 | 44381793 | |||||
chr7:44381890
|
C | G | 4 | a0003c0003t0005a0003c0003t0006a0003c0003t0009others(1): Show | 17 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(14): Show |
3_prime_UTR_variant | MODIFIER | c.*4121G>C | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 6/6 | 4121 | chr7 | 44381890 | |||||
chr7:44381984
|
G | A | 1 | a0001c0001t0015 | 2 | HG01257.hp2 HG01258.hp1 |
3_prime_UTR_variant | MODIFIER | c.*4027C>T | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 6/6 | 4027 | chr7 | 44381984 | |||||
chr7:44382072
|
T | C | 1 | a0001c0001t0032 | 1 | HG01109.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3939A>G | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 6/6 | 3939 | chr7 | 44382072 | |||||
chr7:44382131
|
G | T | 1 | a0001c0001t0026 | 1 | HG01978.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3880C>A | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 6/6 | 3880 | chr7 | 44382131 | |||||
chr7:44382231
|
A | C | 1 | a0001c0001t0025 | 1 | HG03831.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3780T>G | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 6/6 | 3780 | chr7 | 44382231 | |||||
chr7:44382239
|
T | A | 1 | a0001c0001t0033 | 1 | HG03453.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3772A>T | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 6/6 | 3772 | chr7 | 44382239 | |||||
chr7:44382332
|
A | G | 2 | a0002c0002t0021a0002c0002t0040 | 2 | HG03486.hp1 NA21309.hp1 |
3_prime_UTR_variant | MODIFIER | c.*3679T>C | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 6/6 | 3679 | chr7 | 44382332 | |||||
chr7:44382335
|
G | GA | 3 | a0001c0001t0003a0001c0001t0034a0004c0004t0003 | 14 | HG00323.hp2 HG00639.hp1 HG02165.hp1 others(11): Show |
3_prime_UTR_variant | MODIFIER | c.*3675dupT | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 6/6 | 3675 | chr7 | 44382335 | |||||
chr7:44382419
|
C | T | 4 | a0002c0002t0004a0002c0002t0020a0002c0002t0022others(1): Show | 11 | HG00735.hp2 HG01070.hp2 HG01071.hp1 others(8): Show |
3_prime_UTR_variant | MODIFIER | c.*3592G>A | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 6/6 | 3592 | chr7 | 44382419 | |||||
chr7:44382475
|
A | G | 6 | a0002c0002t0021a0002c0002t0040a0003c0003t0005others(3): Show | 19 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(16): Show |
3_prime_UTR_variant | MODIFIER | c.*3536T>C | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 6/6 | 3536 | chr7 | 44382475 | |||||
chr7:44382502
|
G | A | 1 | a0001c0001t0016 | 2 | HG00642.hp1 HG01175.hp1 |
3_prime_UTR_variant | MODIFIER | c.*3509C>T | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 6/6 | 3509 | chr7 | 44382502 | |||||
chr7:44382518
|
T | C | 1 | a0002c0002t0007 | 3 | HG03453.hp1 HG03516.hp1 NA19043.hp1 |
3_prime_UTR_variant | MODIFIER | c.*3493A>G | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 6/6 | 3493 | chr7 | 44382518 | |||||
chr7:44382628
|
C | T | 1 | a0002c0002t0018 | 2 | HG02895.hp1 HG06807.hp2 |
3_prime_UTR_variant | MODIFIER | c.*3383G>A | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 6/6 | 3383 | chr7 | 44382628 | |||||
chr7:44382650
|
G | T | 1 | a0002c0002t0023 | 1 | HG03130.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3361C>A | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 6/6 | 3361 | chr7 | 44382650 | |||||
chr7:44382705
|
G | A | 1 | a0002c0002t0023 | 1 | HG03130.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3306C>T | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 6/6 | 3306 | chr7 | 44382705 | |||||
chr7:44383164
|
C | T | 1 | a0002c0002t0008 | 3 | HG02257.hp1 NA18522.hp2 NA21309.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2847G>A | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 6/6 | 2847 | chr7 | 44383164 | |||||
chr7:44383194
|
G | A | 3 | a0002c0002t0007a0002c0002t0010a0002c0002t0011 | 7 | HG00741.hp2 HG02486.hp2 HG02622.hp1 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*2817C>T | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 6/6 | 2817 | chr7 | 44383194 | |||||
chr7:44383229
|
G | C | 2 | a0001c0001t0013a0001c0001t0017 | 4 | HG02109.hp2 HG02622.hp2 HG02809.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*2782C>G | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 6/6 | 2782 | chr7 | 44383229 | |||||
chr7:44383342
|
T | G | 1 | a0001c0001t0035 | 1 | NA19005.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2669A>C | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 6/6 | 2669 | chr7 | 44383342 | |||||
chr7:44383378
|
T | C | 1 | a0001c0001t0036 | 1 | NA18981.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2633A>G | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 6/6 | 2633 | chr7 | 44383378 | |||||
chr7:44383668
|
G | A | 1 | a0002c0002t0021 | 1 | HG03486.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2343C>T | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 6/6 | 2343 | chr7 | 44383668 | |||||
chr7:44383775
|
C | T | 2 | a0002c0002t0021a0002c0002t0040 | 2 | HG03486.hp1 NA21309.hp1 |
3_prime_UTR_variant | MODIFIER | c.*2236G>A | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 6/6 | 2236 | chr7 | 44383775 | |||||
chr7:44383849
|
G | A | 1 | a0002c0002t0040 | 1 | NA21309.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2162C>T | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 6/6 | 2162 | chr7 | 44383849 | |||||
chr7:44383858
|
C | T | 2 | a0001c0001t0024a0002c0002t0010 | 3 | HG00741.hp2 HG03139.hp1 HG03831.hp1 |
3_prime_UTR_variant | MODIFIER | c.*2153G>A | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 6/6 | 2153 | chr7 | 44383858 | |||||
chr7:44383859
|
G | A | 1 | a0001c0001t0039 | 1 | NA18970.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2152C>T | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 6/6 | 2152 | chr7 | 44383859 | |||||
chr7:44383883
|
C | T | 1 | a0002c0002t0010 | 2 | HG00741.hp2 HG03139.hp1 |
3_prime_UTR_variant | MODIFIER | c.*2128G>A | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 6/6 | 2128 | chr7 | 44383883 | |||||
chr7:44384195
|
G | A | 1 | a0001c0001t0037 | 1 | NA20905.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1816C>T | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 6/6 | 1816 | chr7 | 44384195 | |||||
chr7:44384228
|
C | G | 1 | a0001c0001t0013 | 2 | HG02622.hp2 HG02809.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1783G>C | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 6/6 | 1783 | chr7 | 44384228 | |||||
chr7:44384459
|
C | A | 1 | a0002c0002t0023 | 1 | HG03130.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1552G>T | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 6/6 | 1552 | chr7 | 44384459 | |||||
chr7:44384488
|
CAT | C | 1 | a0002c0002t0008 | 3 | HG02257.hp1 NA18522.hp2 NA21309.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1521_*1522delAT | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 6/6 | 1521 | chr7 | 44384488 | |||||
chr7:44384612
|
T | C | 17 | a0002c0002t0004a0002c0002t0007a0002c0002t0008others(14): Show | 45 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(42): Show |
3_prime_UTR_variant | MODIFIER | c.*1399A>G | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 6/6 | 1399 | chr7 | 44384612 | |||||
chr7:44384654
|
C | T | 15 | a0002c0002t0004a0002c0002t0007a0002c0002t0010others(12): Show | 40 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(37): Show |
3_prime_UTR_variant | MODIFIER | c.*1357G>A | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 6/6 | 1357 | chr7 | 44384654 | |||||
chr7:44385338
|
G | A | 3 | a0002c0002t0007a0002c0002t0010a0002c0002t0011 | 7 | HG00741.hp2 HG02486.hp2 HG02622.hp1 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*673C>T | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 6/6 | 673 | chr7 | 44385338 | |||||
chr7:44385370
|
T | C | 1 | a0002c0002t0018 | 2 | HG02895.hp1 HG06807.hp2 |
3_prime_UTR_variant | MODIFIER | c.*641A>G | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 6/6 | 641 | chr7 | 44385370 | |||||
chr7:44385384
|
T | C | 4 | a0003c0003t0005a0003c0003t0006a0003c0003t0009others(1): Show | 17 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(14): Show |
3_prime_UTR_variant | MODIFIER | c.*627A>G | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 6/6 | 627 | chr7 | 44385384 | |||||
chr7:44385489
|
CAA | C | 3 | a0002c0002t0007a0002c0002t0010a0002c0002t0011 | 7 | HG00741.hp2 HG02486.hp2 HG02622.hp1 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*520_*521delTT | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 6/6 | 520 | chr7 | 44385489 | |||||
chr7:44385626
|
T | G | 2 | a0002c0002t0020a0002c0002t0038 | 2 | HG02280.hp2 NA20300.hp1 |
3_prime_UTR_variant | MODIFIER | c.*385A>C | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 6/6 | 385 | chr7 | 44385626 | |||||
chr7:44385736
|
T | C | 1 | a0001c0001t0039 | 1 | NA18970.hp1 | 3_prime_UTR_variant | MODIFIER | c.*275A>G | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 6/6 | 275 | chr7 | 44385736 | |||||
chr7:44385744
|
C | T | 1 | a0002c0002t0020 | 1 | NA20300.hp1 | 3_prime_UTR_variant | MODIFIER | c.*267G>A | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 6/6 | 267 | chr7 | 44385744 | |||||
chr7:44490636
|
G | C | 1 | a0002c0002t0040 | 1 | NA21309.hp1 | 5_prime_UTR_variant | MODIFIER | c.-36C>G | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 1/6 | 36 | chr7 | 44490636 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr7:44386355
|
C | T | 1 | a0002c0002t0040g0237 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.976-234G>A | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 5/5 | chr7 | 44386355 | ||||||
chr7:44386720
|
C | G | 3 | a0001c0001t0001g0121a0001c0001t0001g0132a0001c0001t0001g0139 | 3 | HG02559.hp1 HG02615.hp2 HG02809.hp2 |
intron_variant | MODIFIER | c.976-599G>C | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 5/5 | chr7 | 44386720 | ||||||
chr7:44386757
|
C | T | 1 | a0001c0001t0001g0090 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.976-636G>A | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 5/5 | chr7 | 44386757 | ||||||
chr7:44386971
|
C | T | 1 | a0001c0001t0001g0145 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.976-850G>A | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 5/5 | chr7 | 44386971 | ||||||
chr7:44386989
|
A | G | 1 | a0003c0003t0006g0234 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.976-868T>C | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 5/5 | chr7 | 44386989 | ||||||
chr7:44386997
|
CAA | C | 10 | a0001c0001t0001g0028a0001c0001t0001g0049a0001c0001t0001g0093others(7): Show | 10 | HG00438.hp2 HG01496.hp1 HG01952.hp2 others(7): Show |
intron_variant | MODIFIER | c.976-878_976-877del others(2): Show |
NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 5/5 | chr7 | 44386997 | ||||||
chr7:44387019
|
G | A | 1 | a0002c0002t0021g0217 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.976-898C>T | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 5/5 | chr7 | 44387019 | ||||||
chr7:44387401
|
T | A | 1 | a0001c0001t0002g0099 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.976-1280A>T | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 5/5 | chr7 | 44387401 | ||||||
chr7:44387550
|
G | A | 17 | a0003c0003t0005g0218a0003c0003t0005g0219a0003c0003t0005g0221others(14): Show | 17 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(14): Show |
intron_variant | MODIFIER | c.976-1429C>T | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 5/5 | chr7 | 44387550 | ||||||
chr7:44387693
|
C | A | 17 | a0003c0003t0005g0218a0003c0003t0005g0219a0003c0003t0005g0221others(14): Show | 17 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(14): Show |
intron_variant | MODIFIER | c.976-1572G>T | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 5/5 | chr7 | 44387693 | ||||||
chr7:44387820
|
G | C | 2 | a0002c0002t0021g0217a0002c0002t0040g0237 | 2 | HG03486.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.976-1699C>G | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 5/5 | chr7 | 44387820 | ||||||
chr7:44387900
|
A | T | 31 | a0001c0001t0001g0028a0001c0001t0001g0040a0001c0001t0001g0041others(28): Show | 31 | HG00438.hp2 HG00558.hp1 HG00673.hp1 others(28): Show |
intron_variant | MODIFIER | c.976-1779T>A | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 5/5 | chr7 | 44387900 | ||||||
chr7:44387993
|
G | A | 1 | a0001c0001t0001g0041 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.976-1872C>T | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 5/5 | chr7 | 44387993 | ||||||
chr7:44388046
|
T | A | 1 | a0001c0001t0002g0058 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.976-1925A>T | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 5/5 | chr7 | 44388046 | ||||||
chr7:44388229
|
G | T | 1 | a0001c0001t0001g0166 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.976-2108C>A | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 5/5 | chr7 | 44388229 | ||||||
chr7:44388233
|
G | A | 1 | a0001c0001t0001g0119 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.976-2112C>T | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 5/5 | chr7 | 44388233 | ||||||
chr7:44388258
|
C | T | 6 | a0001c0001t0001g0100a0001c0001t0013g0072a0001c0001t0013g0123others(3): Show | 6 | HG02109.hp2 HG02559.hp2 HG02622.hp2 others(3): Show |
intron_variant | MODIFIER | c.976-2137G>A | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 5/5 | chr7 | 44388258 | ||||||
chr7:44388259
|
G | A | 17 | a0003c0003t0005g0218a0003c0003t0005g0219a0003c0003t0005g0221others(14): Show | 17 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(14): Show |
intron_variant | MODIFIER | c.976-2138C>T | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 5/5 | chr7 | 44388259 | ||||||
chr7:44388435
|
A | G | 2 | a0001c0001t0001g0048a0001c0001t0001g0057 | 2 | HG02922.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.976-2314T>C | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 5/5 | chr7 | 44388435 | ||||||
chr7:44388514
|
C | A | 3 | a0001c0001t0001g0121a0001c0001t0001g0132a0001c0001t0001g0139 | 3 | HG02559.hp1 HG02615.hp2 HG02809.hp2 |
intron_variant | MODIFIER | c.976-2393G>T | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 5/5 | chr7 | 44388514 | ||||||
chr7:44388514
|
C | T | 1 | a0001c0001t0001g0012 | 1 | NA18957.hp2 | intron_variant | MODIFIER | c.976-2393G>A | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 5/5 | chr7 | 44388514 | ||||||
chr7:44388881
|
T | C | 19 | a0002c0002t0021g0217a0002c0002t0040g0237a0003c0003t0005g0218others(16): Show | 19 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(16): Show |
intron_variant | MODIFIER | c.976-2760A>G | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 5/5 | chr7 | 44388881 | ||||||
chr7:44389076
|
T | C | 2 | a0002c0005t0012g0235a0002c0005t0012g0236 | 2 | HG02922.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.976-2955A>G | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 5/5 | chr7 | 44389076 | ||||||
chr7:44389261
|
GAC | G | 17 | a0003c0003t0005g0218a0003c0003t0005g0219a0003c0003t0005g0221others(14): Show | 17 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(14): Show |
intron_variant | MODIFIER | c.975+3034_975+3035d others(4): Show |
NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 5/5 | chr7 | 44389261 | ||||||
chr7:44389282
|
G | A | 2 | a0002c0005t0012g0235a0002c0005t0012g0236 | 2 | HG02922.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.975+3015C>T | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 5/5 | chr7 | 44389282 | ||||||
chr7:44389401
|
G | A | 2 | a0003c0003t0006g0229a0003c0003t0006g0231 | 2 | NA18979.hp2 NA19065.hp2 |
intron_variant | MODIFIER | c.975+2896C>T | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 5/5 | chr7 | 44389401 | ||||||
chr7:44389507
|
T | C | 1 | a0001c0001t0001g0188 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.975+2790A>G | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 5/5 | chr7 | 44389507 | ||||||
chr7:44389691
|
G | C | 17 | a0003c0003t0005g0218a0003c0003t0005g0219a0003c0003t0005g0221others(14): Show | 17 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(14): Show |
intron_variant | MODIFIER | c.975+2606C>G | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 5/5 | chr7 | 44389691 | ||||||
chr7:44389707
|
T | A | 1 | a0001c0001t0001g0157 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.975+2590A>T | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 5/5 | chr7 | 44389707 | ||||||
chr7:44389953
|
T | C | 7 | a0002c0002t0007g0196a0002c0002t0007g0197a0002c0002t0007g0198others(4): Show | 7 | HG00741.hp2 HG02486.hp2 HG02622.hp1 others(4): Show |
intron_variant | MODIFIER | c.975+2344A>G | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 5/5 | chr7 | 44389953 | ||||||
chr7:44389972
|
A | G | 1 | a0001c0001t0001g0021 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.975+2325T>C | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 5/5 | chr7 | 44389972 | ||||||
chr7:44390378
|
A | G | 1 | a0002c0002t0021g0217 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.975+1919T>C | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 5/5 | chr7 | 44390378 | ||||||
chr7:44390445
|
T | C | 1 | a0001c0001t0014g0013 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.975+1852A>G | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 5/5 | chr7 | 44390445 | ||||||
chr7:44390519
|
ACCTTAGT others(1): Show |
A | 9 | a0003c0003t0006g0226a0003c0003t0006g0229a0003c0003t0006g0231others(6): Show | 9 | HG00280.hp2 HG00438.hp1 HG01358.hp2 others(6): Show |
intron_variant | MODIFIER | c.975+1770_975+1777d others(10): Show |
NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 5/5 | chr7 | 44390519 | ||||||
chr7:44390586
|
T | C | 1 | a0004c0004t0003g0026 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.975+1711A>G | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 5/5 | chr7 | 44390586 | ||||||
chr7:44390591
|
T | G | 19 | a0002c0002t0021g0217a0002c0002t0040g0237a0003c0003t0005g0218others(16): Show | 19 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(16): Show |
intron_variant | MODIFIER | c.975+1706A>C | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 5/5 | chr7 | 44390591 | ||||||
chr7:44390592
|
T | C | 36 | a0002c0002t0004g0207a0002c0002t0004g0208a0002c0002t0004g0210others(33): Show | 36 | HG00099.hp2 HG00280.hp1 HG00735.hp2 others(33): Show |
intron_variant | MODIFIER | c.975+1705A>G | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 5/5 | chr7 | 44390592 | ||||||
chr7:44390652
|
G | T | 36 | a0001c0001t0001g0001a0001c0001t0001g0034a0001c0001t0001g0062others(33): Show | 37 | HG00099.hp1 HG00323.hp2 HG00609.hp2 others(34): Show |
intron_variant | MODIFIER | c.975+1645C>A | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 5/5 | chr7 | 44390652 | ||||||
chr7:44390864
|
A | T | 4 | a0001c0001t0001g0014a0001c0001t0001g0015a0001c0001t0001g0124others(1): Show | 4 | HG00544.hp2 HG02155.hp2 NA19060.hp1 others(1): Show |
intron_variant | MODIFIER | c.975+1433T>A | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 5/5 | chr7 | 44390864 | ||||||
chr7:44391060
|
T | G | 1 | a0001c0001t0001g0116 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.975+1237A>C | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 5/5 | chr7 | 44391060 | ||||||
chr7:44391150
|
A | G | 7 | a0002c0002t0007g0196a0002c0002t0007g0197a0002c0002t0007g0198others(4): Show | 7 | HG00741.hp2 HG02486.hp2 HG02622.hp1 others(4): Show |
intron_variant | MODIFIER | c.975+1147T>C | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 5/5 | chr7 | 44391150 | ||||||
chr7:44391179
|
A | C | 3 | a0002c0002t0008g0204a0002c0002t0008g0205a0002c0002t0008g0206 | 3 | HG02257.hp1 NA18522.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.975+1118T>G | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 5/5 | chr7 | 44391179 | ||||||
chr7:44391230
|
G | A | 1 | a0001c0001t0002g0064 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.975+1067C>T | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 5/5 | chr7 | 44391230 | ||||||
chr7:44391330
|
G | A | 1 | a0004c0004t0003g0016 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.975+967C>T | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 5/5 | chr7 | 44391330 | ||||||
chr7:44391360
|
C | T | 18 | a0001c0001t0002g0060a0003c0003t0005g0218a0003c0003t0005g0219others(15): Show | 18 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(15): Show |
intron_variant | MODIFIER | c.975+937G>A | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 5/5 | chr7 | 44391360 | ||||||
chr7:44391365
|
G | A | 1 | a0002c0002t0007g0198 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.975+932C>T | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 5/5 | chr7 | 44391365 | ||||||
chr7:44391464
|
G | T | 3 | a0002c0002t0007g0196a0002c0002t0007g0197a0002c0002t0007g0198 | 3 | HG03453.hp1 HG03516.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.975+833C>A | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 5/5 | chr7 | 44391464 | ||||||
chr7:44391691
|
C | T | 17 | a0003c0003t0005g0218a0003c0003t0005g0219a0003c0003t0005g0221others(14): Show | 17 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(14): Show |
intron_variant | MODIFIER | c.975+606G>A | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 5/5 | chr7 | 44391691 | ||||||
chr7:44391728
|
A | C | 1 | a0001c0001t0001g0046 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.975+569T>G | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 5/5 | chr7 | 44391728 | ||||||
chr7:44391801
|
A | G | 19 | a0002c0002t0021g0217a0002c0002t0040g0237a0003c0003t0005g0218others(16): Show | 19 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(16): Show |
intron_variant | MODIFIER | c.975+496T>C | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 5/5 | chr7 | 44391801 | ||||||
chr7:44391959
|
A | G | 1 | a0002c0002t0021g0217 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.975+338T>C | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 5/5 | chr7 | 44391959 | ||||||
chr7:44392004
|
G | A | 1 | a0002c0002t0021g0217 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.975+293C>T | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 5/5 | chr7 | 44392004 | ||||||
chr7:44392032
|
G | C | 19 | a0002c0002t0021g0217a0002c0002t0040g0237a0003c0003t0005g0218others(16): Show | 19 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(16): Show |
intron_variant | MODIFIER | c.975+265C>G | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 5/5 | chr7 | 44392032 | ||||||
chr7:44392153
|
T | C | 2 | a0001c0001t0001g0101a0001c0001t0001g0187 | 2 | HG01943.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.975+144A>G | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 5/5 | chr7 | 44392153 | ||||||
chr7:44392236
|
C | T | 1 | a0002c0002t0040g0237 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.975+61G>A | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 5/5 | chr7 | 44392236 | ||||||
chr7:44392493
|
C | G | 1 | a0001c0001t0001g0090 | 1 | HG00099.hp1 | splice_region_variant&intron_variant | LOW | c.787-8G>C | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 4/5 | chr7 | 44392493 | ||||||
chr7:44392826
|
A | G | 1 | a0001c0001t0035g0027 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.787-341T>C | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 4/5 | chr7 | 44392826 | ||||||
chr7:44393147
|
C | T | 2 | a0002c0005t0012g0235a0002c0005t0012g0236 | 2 | HG02922.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.787-662G>A | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 4/5 | chr7 | 44393147 | ||||||
chr7:44393214
|
G | C | 1 | a0001c0001t0001g0119 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.787-729C>G | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 4/5 | chr7 | 44393214 | ||||||
chr7:44393247
|
G | A | 1 | a0002c0002t0040g0237 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.787-762C>T | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 4/5 | chr7 | 44393247 | ||||||
chr7:44393274
|
C | T | 1 | a0001c0001t0032g0138 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.787-789G>A | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 4/5 | chr7 | 44393274 | ||||||
chr7:44393654
|
T | C | 2 | a0001c0001t0002g0060a0001c0001t0024g0120 | 2 | HG03831.hp1 NA20805.hp1 |
intron_variant | MODIFIER | c.787-1169A>G | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 4/5 | chr7 | 44393654 | ||||||
chr7:44393697
|
T | A | 2 | a0001c0001t0001g0124a0001c0001t0001g0125 | 2 | NA19060.hp1 NA19077.hp2 |
intron_variant | MODIFIER | c.787-1212A>T | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 4/5 | chr7 | 44393697 | ||||||
chr7:44393865
|
C | T | 2 | a0001c0001t0001g0141a0001c0001t0001g0167 | 2 | HG02015.hp1 HG02056.hp2 |
intron_variant | MODIFIER | c.787-1380G>A | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 4/5 | chr7 | 44393865 | ||||||
chr7:44393950
|
C | T | 1 | a0001c0001t0001g0090 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.787-1465G>A | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 4/5 | chr7 | 44393950 | ||||||
chr7:44394059
|
G | A | 1 | a0001c0001t0001g0166 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.787-1574C>T | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 4/5 | chr7 | 44394059 | ||||||
chr7:44394179
|
C | T | 2 | a0003c0003t0005g0224a0003c0003t0005g0233 | 2 | HG00280.hp1 NA20805.hp2 |
intron_variant | MODIFIER | c.787-1694G>A | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 4/5 | chr7 | 44394179 | ||||||
chr7:44394345
|
C | G | 1 | a0001c0001t0027g0146 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.787-1860G>C | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 4/5 | chr7 | 44394345 | ||||||
chr7:44394373
|
G | T | 1 | a0001c0001t0001g0116 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.787-1888C>A | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 4/5 | chr7 | 44394373 | ||||||
chr7:44394417
|
C | T | 1 | a0002c0002t0021g0217 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.787-1932G>A | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 4/5 | chr7 | 44394417 | ||||||
chr7:44394580
|
G | A | 1 | a0001c0001t0001g0162 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.787-2095C>T | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 4/5 | chr7 | 44394580 | ||||||
chr7:44394632
|
C | T | 17 | a0003c0003t0005g0218a0003c0003t0005g0219a0003c0003t0005g0221others(14): Show | 17 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(14): Show |
intron_variant | MODIFIER | c.787-2147G>A | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 4/5 | chr7 | 44394632 | ||||||
chr7:44394692
|
A | C | 11 | a0002c0002t0004g0207a0002c0002t0004g0208a0002c0002t0004g0210others(8): Show | 11 | HG00735.hp2 HG01070.hp2 HG01071.hp1 others(8): Show |
intron_variant | MODIFIER | c.787-2207T>G | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 4/5 | chr7 | 44394692 | ||||||
chr7:44394757
|
C | T | 2 | a0003c0003t0005g0224a0003c0003t0005g0233 | 2 | HG00280.hp1 NA20805.hp2 |
intron_variant | MODIFIER | c.787-2272G>A | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 4/5 | chr7 | 44394757 | ||||||
chr7:44394811
|
G | A | 1 | a0001c0001t0026g0186 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.787-2326C>T | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 4/5 | chr7 | 44394811 | ||||||
chr7:44394866
|
C | A | 1 | a0001c0001t0001g0036 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.787-2381G>T | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 4/5 | chr7 | 44394866 | ||||||
chr7:44394885
|
C | T | 3 | a0002c0002t0007g0196a0002c0002t0007g0197a0002c0002t0007g0198 | 3 | HG03453.hp1 HG03516.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.787-2400G>A | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 4/5 | chr7 | 44394885 | ||||||
chr7:44395071
|
C | G | 40 | a0002c0002t0004g0207a0002c0002t0004g0208a0002c0002t0004g0210others(37): Show | 40 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(37): Show |
intron_variant | MODIFIER | c.787-2586G>C | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 4/5 | chr7 | 44395071 | ||||||
chr7:44395121
|
T | C | 1 | a0002c0002t0040g0237 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.787-2636A>G | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 4/5 | chr7 | 44395121 | ||||||
chr7:44395129
|
T | C | 19 | a0002c0002t0021g0217a0002c0002t0040g0237a0003c0003t0005g0218others(16): Show | 19 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(16): Show |
intron_variant | MODIFIER | c.787-2644A>G | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 4/5 | chr7 | 44395129 | ||||||
chr7:44395358
|
A | C | 2 | a0001c0001t0001g0097a0001c0001t0028g0111 | 2 | NA18955.hp1 NA19063.hp2 |
intron_variant | MODIFIER | c.787-2873T>G | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 4/5 | chr7 | 44395358 | ||||||
chr7:44395376
|
T | C | 1 | a0001c0001t0001g0130 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.787-2891A>G | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 4/5 | chr7 | 44395376 | ||||||
chr7:44395476
|
A | G | 1 | a0001c0001t0027g0146 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.787-2991T>C | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 4/5 | chr7 | 44395476 | ||||||
chr7:44395667
|
TAC | T | 3 | a0002c0002t0007g0196a0002c0002t0007g0197a0002c0002t0007g0198 | 3 | HG03453.hp1 HG03516.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.787-3184_787-3183d others(4): Show |
NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 4/5 | chr7 | 44395667 | ||||||
chr7:44395670
|
A | T | 17 | a0003c0003t0005g0218a0003c0003t0005g0219a0003c0003t0005g0221others(14): Show | 17 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(14): Show |
intron_variant | MODIFIER | c.787-3185T>A | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 4/5 | chr7 | 44395670 | ||||||
chr7:44396051
|
T | C | 1 | a0002c0002t0004g0207 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.787-3566A>G | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 4/5 | chr7 | 44396051 | ||||||
chr7:44396087
|
T | TTG | 14 | a0001c0001t0001g0010a0001c0001t0001g0022a0001c0001t0001g0051others(11): Show | 14 | HG01109.hp2 HG01168.hp1 HG01169.hp1 others(11): Show |
intron_variant | MODIFIER | c.787-3604_787-3603d others(4): Show |
NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 4/5 | chr7 | 44396087 | ||||||
chr7:44396087
|
T | TTGTG | 18 | a0001c0001t0001g0037a0001c0001t0001g0038a0001c0001t0001g0039others(15): Show | 18 | HG00735.hp2 HG00741.hp2 HG01071.hp2 others(15): Show |
intron_variant | MODIFIER | c.787-3606_787-3603d others(6): Show |
NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 4/5 | chr7 | 44396087 | ||||||
chr7:44396087
|
T | TTGTGTG | 9 | a0001c0001t0001g0035a0002c0002t0004g0207a0002c0002t0004g0208others(6): Show | 9 | HG02683.hp2 HG03654.hp1 HG03942.hp1 others(6): Show |
intron_variant | MODIFIER | c.787-3608_787-3603d others(8): Show |
NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 4/5 | chr7 | 44396087 | ||||||
chr7:44396087
|
T | TTGTGTGT others(1): Show |
2 | a0001c0001t0001g0036a0002c0002t0023g0209 | 2 | HG02572.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.787-3610_787-3603d others(10): Show |
NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 4/5 | chr7 | 44396087 | ||||||
chr7:44396087
|
T | TTGTGTGT others(3): Show |
2 | a0002c0002t0011g0194a0002c0002t0011g0195 | 2 | HG02486.hp2 HG02622.hp1 |
intron_variant | MODIFIER | c.787-3612_787-3603d others(12): Show |
NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 4/5 | chr7 | 44396087 | ||||||
chr7:44396087
|
T | TTGTGTGT others(7): Show |
3 | a0002c0002t0008g0204a0002c0002t0008g0205a0002c0002t0008g0206 | 3 | HG02257.hp1 NA18522.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.787-3616_787-3603d others(16): Show |
NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 4/5 | chr7 | 44396087 | ||||||
chr7:44396087
|
TTG | T | 70 | a0001c0001t0001g0001a0001c0001t0001g0017a0001c0001t0001g0018others(67): Show | 71 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(68): Show |
intron_variant | MODIFIER | c.787-3604_787-3603d others(4): Show |
NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 4/5 | chr7 | 44396087 | ||||||
chr7:44396087
|
TTGTG | T | 3 | a0001c0001t0002g0060a0003c0003t0005g0218a0003c0003t0005g0219 | 3 | HG03491.hp1 HG03492.hp2 NA20805.hp1 |
intron_variant | MODIFIER | c.787-3606_787-3603d others(6): Show |
NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 4/5 | chr7 | 44396087 | ||||||
chr7:44396087
|
TTGTGTG | T | 4 | a0001c0001t0001g0050a0001c0001t0001g0109a0002c0002t0007g0196others(1): Show | 4 | HG02145.hp2 HG03453.hp1 HG03516.hp1 others(1): Show |
intron_variant | MODIFIER | c.787-3608_787-3603d others(8): Show |
NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 4/5 | chr7 | 44396087 | ||||||
chr7:44396087
|
TTGTGTGT others(5): Show |
T | 1 | a0002c0002t0007g0198 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.787-3614_787-3603d others(14): Show |
NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 4/5 | chr7 | 44396087 | ||||||
chr7:44396087
|
TTGTGTGT others(7): Show |
T | 3 | a0001c0001t0002g0061a0001c0001t0002g0078a0001c0001t0002g0122 | 3 | HG00544.hp1 HG02056.hp1 HG02523.hp2 |
intron_variant | MODIFIER | c.787-3616_787-3603d others(16): Show |
NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 4/5 | chr7 | 44396087 | ||||||
chr7:44396113
|
G | GTGTC | 3 | a0001c0001t0002g0184a0004c0004t0003g0025a0004c0004t0003g0026 | 3 | HG00639.hp1 HG00639.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.787-3629_787-3628i others(6): Show |
NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 4/5 | chr7 | 44396113 | ||||||
chr7:44396117
|
GTGTGTGT others(3): Show |
G | 1 | a0001c0001t0001g0075 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.787-3642_787-3633d others(12): Show |
NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 4/5 | chr7 | 44396117 | ||||||
chr7:44396123
|
GTGT | G | 2 | a0001c0001t0001g0108a0001c0001t0001g0114 | 2 | NA18965.hp2 NA19074.hp2 |
intron_variant | MODIFIER | c.787-3641_787-3639d others(5): Show |
NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 4/5 | chr7 | 44396123 | ||||||
chr7:44396123
|
GTGTT | G | 7 | a0001c0001t0001g0147a0001c0001t0001g0148a0001c0001t0001g0150others(4): Show | 7 | HG02155.hp1 NA18955.hp2 NA18965.hp1 others(4): Show |
intron_variant | MODIFIER | c.787-3642_787-3639d others(6): Show |
NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 4/5 | chr7 | 44396123 | ||||||
chr7:44396125
|
GT | G | 4 | a0001c0001t0001g0095a0001c0001t0001g0107a0001c0001t0001g0116others(1): Show | 4 | HG03927.hp1 NA18941.hp1 NA18985.hp2 others(1): Show |
intron_variant | MODIFIER | c.787-3641delA | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 4/5 | chr7 | 44396125 | ||||||
chr7:44396126
|
T | TG | 3 | a0001c0001t0001g0023a0001c0001t0001g0110a0001c0001t0001g0153 | 3 | NA18941.hp2 NA18957.hp1 NA18975.hp2 |
intron_variant | MODIFIER | c.787-3642_787-3641i others(3): Show |
NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 4/5 | chr7 | 44396126 | ||||||
chr7:44396127
|
T | G | 5 | a0001c0001t0001g0051a0001c0001t0001g0126a0001c0001t0001g0137others(2): Show | 5 | HG00741.hp2 HG01169.hp2 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.787-3642A>C | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 4/5 | chr7 | 44396127 | ||||||
chr7:44396191
|
C | T | 2 | a0002c0002t0004g0214a0002c0002t0022g0215 | 2 | HG01109.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.787-3706G>A | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 4/5 | chr7 | 44396191 | ||||||
chr7:44396484
|
G | A | 3 | a0001c0001t0001g0156a0001c0001t0001g0158a0001c0001t0001g0159 | 3 | HG03834.hp1 HG04204.hp2 NA20905.hp1 |
intron_variant | MODIFIER | c.787-3999C>T | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 4/5 | chr7 | 44396484 | ||||||
chr7:44396737
|
C | T | 3 | a0002c0002t0007g0196a0002c0002t0007g0197a0002c0002t0007g0198 | 3 | HG03453.hp1 HG03516.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.787-4252G>A | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 4/5 | chr7 | 44396737 | ||||||
chr7:44396786
|
C | T | 1 | a0001c0001t0001g0094 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.787-4301G>A | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 4/5 | chr7 | 44396786 | ||||||
chr7:44396803
|
T | C | 2 | a0002c0002t0004g0213a0002c0002t0004g0216 | 2 | HG01070.hp2 HG01071.hp1 |
intron_variant | MODIFIER | c.787-4318A>G | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 4/5 | chr7 | 44396803 | ||||||
chr7:44396815
|
A | G | 1 | a0002c0002t0040g0237 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.787-4330T>C | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 4/5 | chr7 | 44396815 | ||||||
chr7:44396878
|
A | G | 1 | a0002c0002t0040g0237 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.787-4393T>C | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 4/5 | chr7 | 44396878 | ||||||
chr7:44396898
|
C | T | 4 | a0001c0001t0002g0065a0001c0001t0002g0076a0001c0001t0002g0091others(1): Show | 4 | HG01109.hp1 HG01358.hp1 HG01515.hp2 others(1): Show |
intron_variant | MODIFIER | c.787-4413G>A | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 4/5 | chr7 | 44396898 | ||||||
chr7:44396908
|
A | G | 2 | a0003c0003t0005g0218a0003c0003t0005g0219 | 2 | HG03491.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.787-4423T>C | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 4/5 | chr7 | 44396908 | ||||||
chr7:44396948
|
T | C | 2 | a0002c0002t0021g0217a0002c0002t0040g0237 | 2 | HG03486.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.787-4463A>G | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 4/5 | chr7 | 44396948 | ||||||
chr7:44396951
|
TTG | T | 19 | a0002c0002t0021g0217a0002c0002t0040g0237a0003c0003t0005g0218others(16): Show | 19 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(16): Show |
intron_variant | MODIFIER | c.787-4468_787-4467d others(4): Show |
NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 4/5 | chr7 | 44396951 | ||||||
chr7:44397060
|
A | G | 1 | a0001c0001t0001g0093 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.787-4575T>C | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 4/5 | chr7 | 44397060 | ||||||
chr7:44398086
|
T | C | 1 | a0002c0002t0023g0209 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.787-5601A>G | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 4/5 | chr7 | 44398086 | ||||||
chr7:44398321
|
G | A | 2 | a0001c0001t0013g0072a0001c0001t0013g0123 | 2 | HG02622.hp2 HG02809.hp1 |
intron_variant | MODIFIER | c.787-5836C>T | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 4/5 | chr7 | 44398321 | ||||||
chr7:44398827
|
G | A | 17 | a0003c0003t0005g0218a0003c0003t0005g0219a0003c0003t0005g0221others(14): Show | 17 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(14): Show |
intron_variant | MODIFIER | c.786+5613C>T | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 4/5 | chr7 | 44398827 | ||||||
chr7:44398991
|
T | C | 1 | a0003c0003t0006g0234 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.786+5449A>G | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 4/5 | chr7 | 44398991 | ||||||
chr7:44399024
|
T | C | 3 | a0002c0002t0023g0209a0002c0005t0012g0235a0002c0005t0012g0236 | 3 | HG02922.hp2 HG03130.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.786+5416A>G | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 4/5 | chr7 | 44399024 | ||||||
chr7:44399103
|
C | T | 1 | a0001c0001t0003g0030 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.786+5337G>A | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 4/5 | chr7 | 44399103 | ||||||
chr7:44399160
|
G | A | 2 | a0001c0001t0001g0054a0001c0001t0001g0140 | 2 | HG02976.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.786+5280C>T | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 4/5 | chr7 | 44399160 | ||||||
chr7:44399279
|
T | C | 1 | a0002c0002t0021g0217 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.786+5161A>G | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 4/5 | chr7 | 44399279 | ||||||
chr7:44399498
|
G | A | 11 | a0002c0002t0004g0207a0002c0002t0004g0208a0002c0002t0004g0210others(8): Show | 11 | HG00735.hp2 HG01070.hp2 HG01071.hp1 others(8): Show |
intron_variant | MODIFIER | c.786+4942C>T | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 4/5 | chr7 | 44399498 | ||||||
chr7:44399621
|
A | G | 1 | a0002c0002t0021g0217 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.786+4819T>C | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 4/5 | chr7 | 44399621 | ||||||
chr7:44399633
|
T | C | 43 | a0002c0002t0004g0207a0002c0002t0004g0208a0002c0002t0004g0210others(40): Show | 43 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(40): Show |
intron_variant | MODIFIER | c.786+4807A>G | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 4/5 | chr7 | 44399633 | ||||||
chr7:44399689
|
G | A | 1 | a0001c0001t0001g0018 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.786+4751C>T | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 4/5 | chr7 | 44399689 | ||||||
chr7:44399914
|
A | G | 1 | a0001c0001t0001g0119 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.786+4526T>C | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 4/5 | chr7 | 44399914 | ||||||
chr7:44399988
|
T | C | 3 | a0001c0001t0001g0106a0001c0001t0001g0113a0001c0001t0031g0103 | 3 | HG01070.hp1 HG01081.hp1 HG01981.hp1 |
intron_variant | MODIFIER | c.786+4452A>G | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 4/5 | chr7 | 44399988 | ||||||
chr7:44399996
|
C | T | 17 | a0003c0003t0005g0218a0003c0003t0005g0219a0003c0003t0005g0221others(14): Show | 17 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(14): Show |
intron_variant | MODIFIER | c.786+4444G>A | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 4/5 | chr7 | 44399996 | ||||||
chr7:44400417
|
A | G | 26 | a0002c0002t0007g0196a0002c0002t0007g0197a0002c0002t0007g0198others(23): Show | 26 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(23): Show |
intron_variant | MODIFIER | c.786+4023T>C | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 4/5 | chr7 | 44400417 | ||||||
chr7:44400758
|
C | T | 5 | a0002c0002t0007g0196a0002c0002t0007g0197a0002c0002t0007g0198others(2): Show | 5 | HG02486.hp2 HG02622.hp1 HG03453.hp1 others(2): Show |
intron_variant | MODIFIER | c.786+3682G>A | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 4/5 | chr7 | 44400758 | ||||||
chr7:44400899
|
T | C | 1 | a0001c0001t0003g0030 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.786+3541A>G | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 4/5 | chr7 | 44400899 | ||||||
chr7:44400952
|
C | T | 17 | a0003c0003t0005g0218a0003c0003t0005g0219a0003c0003t0005g0221others(14): Show | 17 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(14): Show |
intron_variant | MODIFIER | c.786+3488G>A | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 4/5 | chr7 | 44400952 | ||||||
chr7:44400953
|
C | G | 1 | a0001c0001t0001g0174 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.786+3487G>C | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 4/5 | chr7 | 44400953 | ||||||
chr7:44401100
|
G | C | 1 | a0001c0001t0002g0122 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.786+3340C>G | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 4/5 | chr7 | 44401100 | ||||||
chr7:44401185
|
C | G | 1 | a0001c0001t0001g0001 | 2 | HG01516.hp2 HG01517.hp2 |
intron_variant | MODIFIER | c.786+3255G>C | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 4/5 | chr7 | 44401185 | ||||||
chr7:44401186
|
C | A | 1 | a0001c0001t0001g0001 | 2 | HG01516.hp2 HG01517.hp2 |
intron_variant | MODIFIER | c.786+3254G>T | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 4/5 | chr7 | 44401186 | ||||||
chr7:44401199
|
C | G | 2 | a0002c0002t0021g0217a0002c0002t0040g0237 | 2 | HG03486.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.786+3241G>C | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 4/5 | chr7 | 44401199 | ||||||
chr7:44401206
|
C | G | 2 | a0001c0001t0001g0083a0001c0001t0001g0086 | 2 | HG02683.hp1 HG03942.hp2 |
intron_variant | MODIFIER | c.786+3234G>C | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 4/5 | chr7 | 44401206 | ||||||
chr7:44401416
|
T | C | 1 | a0002c0002t0004g0212 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.786+3024A>G | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 4/5 | chr7 | 44401416 | ||||||
chr7:44401429
|
C | T | 1 | a0002c0002t0023g0209 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.786+3011G>A | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 4/5 | chr7 | 44401429 | ||||||
chr7:44401572
|
C | T | 1 | a0001c0001t0001g0006 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.786+2868G>A | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 4/5 | chr7 | 44401572 | ||||||
chr7:44402056
|
T | C | 2 | a0002c0005t0012g0235a0002c0005t0012g0236 | 2 | HG02922.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.786+2384A>G | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 4/5 | chr7 | 44402056 | ||||||
chr7:44402067
|
G | T | 3 | a0002c0002t0008g0204a0002c0002t0008g0205a0002c0002t0008g0206 | 3 | HG02257.hp1 NA18522.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.786+2373C>A | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 4/5 | chr7 | 44402067 | ||||||
chr7:44402410
|
C | T | 1 | a0001c0001t0001g0119 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.786+2030G>A | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 4/5 | chr7 | 44402410 | ||||||
chr7:44402675
|
G | C | 1 | a0002c0002t0040g0237 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.786+1765C>G | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 4/5 | chr7 | 44402675 | ||||||
chr7:44402697
|
A | C | 205 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(202): Show | 206 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(203): Show |
intron_variant | MODIFIER | c.786+1743T>G | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 4/5 | chr7 | 44402697 | ||||||
chr7:44403000
|
T | C | 40 | a0002c0002t0004g0207a0002c0002t0004g0208a0002c0002t0004g0210others(37): Show | 40 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(37): Show |
intron_variant | MODIFIER | c.786+1440A>G | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 4/5 | chr7 | 44403000 | ||||||
chr7:44403068
|
G | A | 3 | a0002c0002t0008g0204a0002c0002t0008g0205a0002c0002t0008g0206 | 3 | HG02257.hp1 NA18522.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.786+1372C>T | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 4/5 | chr7 | 44403068 | ||||||
chr7:44403081
|
G | A | 2 | a0002c0002t0021g0217a0002c0002t0040g0237 | 2 | HG03486.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.786+1359C>T | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 4/5 | chr7 | 44403081 | ||||||
chr7:44403135
|
C | T | 2 | a0002c0002t0011g0194a0002c0002t0011g0195 | 2 | HG02486.hp2 HG02622.hp1 |
intron_variant | MODIFIER | c.786+1305G>A | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 4/5 | chr7 | 44403135 | ||||||
chr7:44403231
|
T | C | 1 | a0001c0001t0001g0187 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.786+1209A>G | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 4/5 | chr7 | 44403231 | ||||||
chr7:44403304
|
T | C | 1 | a0002c0002t0021g0217 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.786+1136A>G | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 4/5 | chr7 | 44403304 | ||||||
chr7:44403514
|
C | G | 1 | a0002c0002t0040g0237 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.786+926G>C | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 4/5 | chr7 | 44403514 | ||||||
chr7:44403544
|
C | T | 17 | a0003c0003t0005g0218a0003c0003t0005g0219a0003c0003t0005g0221others(14): Show | 17 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(14): Show |
intron_variant | MODIFIER | c.786+896G>A | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 4/5 | chr7 | 44403544 | ||||||
chr7:44403546
|
T | C | 19 | a0002c0002t0021g0217a0002c0002t0040g0237a0003c0003t0005g0218others(16): Show | 19 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(16): Show |
intron_variant | MODIFIER | c.786+894A>G | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 4/5 | chr7 | 44403546 | ||||||
chr7:44403559
|
G | A | 5 | a0002c0002t0008g0204a0002c0002t0008g0205a0002c0002t0008g0206others(2): Show | 5 | HG02257.hp1 HG03486.hp1 NA18522.hp2 others(2): Show |
intron_variant | MODIFIER | c.786+881C>T | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 4/5 | chr7 | 44403559 | ||||||
chr7:44403572
|
G | A | 1 | a0001c0001t0026g0186 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.786+868C>T | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 4/5 | chr7 | 44403572 | ||||||
chr7:44403777
|
T | A | 3 | a0002c0002t0007g0196a0002c0002t0007g0197a0002c0002t0007g0198 | 3 | HG03453.hp1 HG03516.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.786+663A>T | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 4/5 | chr7 | 44403777 | ||||||
chr7:44403831
|
G | A | 1 | a0001c0001t0001g0001 | 2 | HG01516.hp2 HG01517.hp2 |
intron_variant | MODIFIER | c.786+609C>T | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 4/5 | chr7 | 44403831 | ||||||
chr7:44403856
|
A | G | 9 | a0003c0003t0006g0226a0003c0003t0006g0229a0003c0003t0006g0231others(6): Show | 9 | HG00280.hp2 HG00438.hp1 HG01358.hp2 others(6): Show |
intron_variant | MODIFIER | c.786+584T>C | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 4/5 | chr7 | 44403856 | ||||||
chr7:44404138
|
C | A | 1 | a0001c0001t0001g0137 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.786+302G>T | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 4/5 | chr7 | 44404138 | ||||||
chr7:44404171
|
G | C | 19 | a0002c0002t0021g0217a0002c0002t0040g0237a0003c0003t0005g0218others(16): Show | 19 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(16): Show |
intron_variant | MODIFIER | c.786+269C>G | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 4/5 | chr7 | 44404171 | ||||||
chr7:44404712
|
C | T | 1 | a0001c0001t0001g0130 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.643-129G>A | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 3/5 | chr7 | 44404712 | ||||||
chr7:44404780
|
A | AG | 236 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(233): Show | 237 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(234): Show |
intron_variant | MODIFIER | c.643-198dupC | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 3/5 | chr7 | 44404780 | ||||||
chr7:44404969
|
A | G | 89 | a0001c0001t0001g0001a0001c0001t0001g0017a0001c0001t0001g0018others(86): Show | 90 | HG00099.hp1 HG00323.hp2 HG00438.hp2 others(87): Show |
intron_variant | MODIFIER | c.643-386T>C | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 3/5 | chr7 | 44404969 | ||||||
chr7:44405103
|
T | C | 1 | a0001c0001t0026g0186 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.643-520A>G | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 3/5 | chr7 | 44405103 | ||||||
chr7:44405250
|
C | A | 1 | a0002c0002t0040g0237 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.643-667G>T | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 3/5 | chr7 | 44405250 | ||||||
chr7:44405305
|
C | T | 1 | a0002c0002t0023g0209 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.643-722G>A | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 3/5 | chr7 | 44405305 | ||||||
chr7:44405343
|
G | A | 2 | a0001c0001t0003g0175a0001c0001t0003g0176 | 2 | NA18974.hp1 NA19003.hp1 |
intron_variant | MODIFIER | c.643-760C>T | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 3/5 | chr7 | 44405343 | ||||||
chr7:44405487
|
T | C | 1 | a0001c0001t0002g0059 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.643-904A>G | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 3/5 | chr7 | 44405487 | ||||||
chr7:44405885
|
C | T | 2 | a0002c0002t0011g0194a0002c0002t0011g0195 | 2 | HG02486.hp2 HG02622.hp1 |
intron_variant | MODIFIER | c.643-1302G>A | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 3/5 | chr7 | 44405885 | ||||||
chr7:44406124
|
T | C | 1 | a0001c0001t0001g0090 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.643-1541A>G | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 3/5 | chr7 | 44406124 | ||||||
chr7:44406185
|
G | A | 1 | a0001c0001t0001g0155 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.643-1602C>T | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 3/5 | chr7 | 44406185 | ||||||
chr7:44406248
|
T | C | 1 | a0001c0001t0001g0021 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.643-1665A>G | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 3/5 | chr7 | 44406248 | ||||||
chr7:44406252
|
C | T | 17 | a0003c0003t0005g0218a0003c0003t0005g0219a0003c0003t0005g0221others(14): Show | 17 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(14): Show |
intron_variant | MODIFIER | c.643-1669G>A | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 3/5 | chr7 | 44406252 | ||||||
chr7:44406481
|
A | G | 2 | a0001c0001t0001g0179a0001c0001t0037g0081 | 2 | HG02738.hp2 NA20905.hp2 |
intron_variant | MODIFIER | c.643-1898T>C | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 3/5 | chr7 | 44406481 | ||||||
chr7:44406536
|
C | A | 3 | a0002c0002t0007g0196a0002c0002t0007g0197a0002c0002t0007g0198 | 3 | HG03453.hp1 HG03516.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.643-1953G>T | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 3/5 | chr7 | 44406536 | ||||||
chr7:44406782
|
G | C | 1 | a0002c0002t0021g0217 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.643-2199C>G | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 3/5 | chr7 | 44406782 | ||||||
chr7:44406786
|
A | G | 1 | a0001c0001t0001g0008 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.643-2203T>C | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 3/5 | chr7 | 44406786 | ||||||
chr7:44406805
|
G | A | 1 | a0001c0001t0001g0062 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.643-2222C>T | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 3/5 | chr7 | 44406805 | ||||||
chr7:44406883
|
A | C | 1 | a0001c0001t0001g0191 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.643-2300T>G | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 3/5 | chr7 | 44406883 | ||||||
chr7:44406976
|
C | T | 2 | a0002c0002t0021g0217a0002c0002t0040g0237 | 2 | HG03486.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.643-2393G>A | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 3/5 | chr7 | 44406976 | ||||||
chr7:44407028
|
A | G | 1 | a0002c0002t0021g0217 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.643-2445T>C | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 3/5 | chr7 | 44407028 | ||||||
chr7:44407052
|
G | A | 2 | a0002c0002t0004g0214a0002c0002t0022g0215 | 2 | HG01109.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.643-2469C>T | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 3/5 | chr7 | 44407052 | ||||||
chr7:44407185
|
G | A | 2 | a0002c0002t0021g0217a0002c0002t0040g0237 | 2 | HG03486.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.643-2602C>T | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 3/5 | chr7 | 44407185 | ||||||
chr7:44407202
|
C | T | 8 | a0001c0001t0001g0160a0001c0001t0001g0161a0001c0001t0001g0162others(5): Show | 8 | HG00741.hp1 HG01071.hp2 HG01168.hp1 others(5): Show |
intron_variant | MODIFIER | c.643-2619G>A | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 3/5 | chr7 | 44407202 | ||||||
chr7:44407269
|
T | TA | 45 | a0001c0001t0001g0035a0002c0002t0004g0207a0002c0002t0004g0208others(42): Show | 45 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(42): Show |
intron_variant | MODIFIER | c.643-2687dupT | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 3/5 | chr7 | 44407269 | ||||||
chr7:44407431
|
G | A | 1 | a0002c0002t0023g0209 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.643-2848C>T | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 3/5 | chr7 | 44407431 | ||||||
chr7:44407459
|
G | A | 2 | a0002c0002t0021g0217a0002c0002t0040g0237 | 2 | HG03486.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.643-2876C>T | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 3/5 | chr7 | 44407459 | ||||||
chr7:44407466
|
G | A | 1 | a0002c0002t0007g0198 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.643-2883C>T | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 3/5 | chr7 | 44407466 | ||||||
chr7:44407566
|
C | CA | 12 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0054others(9): Show | 12 | HG01358.hp1 HG01496.hp2 HG02257.hp2 others(9): Show |
intron_variant | MODIFIER | c.643-2984dupT | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 3/5 | chr7 | 44407566 | ||||||
chr7:44407578
|
A | C | 2 | a0002c0005t0012g0235a0002c0005t0012g0236 | 2 | HG02922.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.643-2995T>G | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 3/5 | chr7 | 44407578 | ||||||
chr7:44407688
|
T | G | 1 | a0001c0001t0001g0050 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.643-3105A>C | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 3/5 | chr7 | 44407688 | ||||||
chr7:44407957
|
A | C | 2 | a0001c0001t0017g0068a0001c0001t0017g0069 | 2 | HG02109.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.643-3374T>G | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 3/5 | chr7 | 44407957 | ||||||
chr7:44408182
|
A | T | 17 | a0003c0003t0005g0218a0003c0003t0005g0219a0003c0003t0005g0221others(14): Show | 17 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(14): Show |
intron_variant | MODIFIER | c.643-3599T>A | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 3/5 | chr7 | 44408182 | ||||||
chr7:44408335
|
C | T | 1 | a0002c0002t0008g0204 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.643-3752G>A | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 3/5 | chr7 | 44408335 | ||||||
chr7:44408625
|
A | G | 1 | a0001c0001t0001g0119 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.643-4042T>C | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 3/5 | chr7 | 44408625 | ||||||
chr7:44409036
|
G | T | 1 | a0001c0001t0001g0152 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.643-4453C>A | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 3/5 | chr7 | 44409036 | ||||||
chr7:44409044
|
A | G | 2 | a0001c0001t0001g0137a0001c0001t0030g0180 | 2 | HG01496.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.643-4461T>C | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 3/5 | chr7 | 44409044 | ||||||
chr7:44409067
|
G | A | 1 | a0001c0001t0002g0189 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.643-4484C>T | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 3/5 | chr7 | 44409067 | ||||||
chr7:44409328
|
T | G | 1 | a0001c0001t0001g0084 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.643-4745A>C | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 3/5 | chr7 | 44409328 | ||||||
chr7:44409565
|
C | CA | 17 | a0001c0001t0001g0017a0001c0001t0001g0035a0001c0001t0001g0046others(14): Show | 17 | HG00741.hp2 HG01496.hp2 HG02486.hp2 others(14): Show |
intron_variant | MODIFIER | c.643-4983dupT | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 3/5 | chr7 | 44409565 | ||||||
chr7:44409863
|
A | G | 1 | a0002c0002t0040g0237 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.643-5280T>C | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 3/5 | chr7 | 44409863 | ||||||
chr7:44409902
|
C | A | 205 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(202): Show | 206 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(203): Show |
intron_variant | MODIFIER | c.643-5319G>T | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 3/5 | chr7 | 44409902 | ||||||
chr7:44409994
|
G | A | 2 | a0001c0001t0001g0001a0001c0001t0001g0090 | 3 | HG00099.hp1 HG01516.hp2 HG01517.hp2 |
intron_variant | MODIFIER | c.643-5411C>T | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 3/5 | chr7 | 44409994 | ||||||
chr7:44410052
|
C | T | 1 | a0002c0002t0040g0237 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.643-5469G>A | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 3/5 | chr7 | 44410052 | ||||||
chr7:44410329
|
T | C | 1 | a0002c0002t0040g0237 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.643-5746A>G | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 3/5 | chr7 | 44410329 | ||||||
chr7:44410695
|
A | G | 19 | a0002c0002t0021g0217a0002c0002t0040g0237a0003c0003t0005g0218others(16): Show | 19 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(16): Show |
intron_variant | MODIFIER | c.643-6112T>C | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 3/5 | chr7 | 44410695 | ||||||
chr7:44410770
|
T | C | 4 | a0001c0001t0001g0147a0001c0001t0001g0171a0001c0001t0001g0182others(1): Show | 4 | NA18965.hp1 NA18989.hp1 NA19063.hp1 others(1): Show |
intron_variant | MODIFIER | c.643-6187A>G | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 3/5 | chr7 | 44410770 | ||||||
chr7:44410785
|
G | T | 1 | a0001c0001t0025g0129 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.643-6202C>A | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 3/5 | chr7 | 44410785 | ||||||
chr7:44410923
|
G | A | 10 | a0001c0001t0001g0036a0001c0001t0001g0037a0001c0001t0001g0038others(7): Show | 10 | HG00639.hp1 HG02109.hp1 HG02145.hp1 others(7): Show |
intron_variant | MODIFIER | c.643-6340C>T | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 3/5 | chr7 | 44410923 | ||||||
chr7:44411063
|
A | T | 2 | a0001c0001t0001g0007a0001c0001t0001g0008 | 2 | NA18970.hp2 NA18983.hp1 |
intron_variant | MODIFIER | c.643-6480T>A | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 3/5 | chr7 | 44411063 | ||||||
chr7:44411230
|
C | T | 29 | a0002c0002t0007g0196a0002c0002t0007g0197a0002c0002t0007g0198others(26): Show | 29 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(26): Show |
intron_variant | MODIFIER | c.643-6647G>A | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 3/5 | chr7 | 44411230 | ||||||
chr7:44411307
|
T | C | 2 | a0001c0001t0002g0011a0001c0001t0002g0047 | 2 | HG01981.hp2 HG03491.hp2 |
intron_variant | MODIFIER | c.643-6724A>G | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 3/5 | chr7 | 44411307 | ||||||
chr7:44411704
|
T | C | 2 | a0003c0003t0005g0222a0003c0003t0005g0223 | 2 | HG01256.hp1 HG01258.hp2 |
intron_variant | MODIFIER | c.643-7121A>G | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 3/5 | chr7 | 44411704 | ||||||
chr7:44411731
|
G | C | 1 | a0001c0001t0030g0180 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.643-7148C>G | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 3/5 | chr7 | 44411731 | ||||||
chr7:44411822
|
T | G | 1 | a0001c0001t0024g0120 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.643-7239A>C | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 3/5 | chr7 | 44411822 | ||||||
chr7:44412092
|
G | T | 1 | a0001c0001t0001g0012 | 1 | NA18957.hp2 | intron_variant | MODIFIER | c.643-7509C>A | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 3/5 | chr7 | 44412092 | ||||||
chr7:44412095
|
C | T | 1 | a0001c0001t0001g0104 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.643-7512G>A | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 3/5 | chr7 | 44412095 | ||||||
chr7:44412513
|
G | A | 17 | a0003c0003t0005g0218a0003c0003t0005g0219a0003c0003t0005g0221others(14): Show | 17 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(14): Show |
intron_variant | MODIFIER | c.643-7930C>T | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 3/5 | chr7 | 44412513 | ||||||
chr7:44412694
|
G | A | 1 | a0001c0001t0001g0041 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.643-8111C>T | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 3/5 | chr7 | 44412694 | ||||||
chr7:44412716
|
AG | A | 7 | a0002c0002t0007g0196a0002c0002t0007g0197a0002c0002t0007g0198others(4): Show | 7 | HG00741.hp2 HG02486.hp2 HG02622.hp1 others(4): Show |
intron_variant | MODIFIER | c.643-8134delC | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 3/5 | chr7 | 44412716 | ||||||
chr7:44412782
|
T | C | 26 | a0002c0002t0007g0196a0002c0002t0007g0197a0002c0002t0007g0198others(23): Show | 26 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(23): Show |
intron_variant | MODIFIER | c.643-8199A>G | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 3/5 | chr7 | 44412782 | ||||||
chr7:44412926
|
C | CAA | 10 | a0001c0001t0001g0174a0002c0002t0004g0207a0002c0002t0004g0208others(7): Show | 10 | HG01070.hp2 HG01071.hp1 HG02280.hp2 others(7): Show |
intron_variant | MODIFIER | c.643-8345_643-8344d others(4): Show |
NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 3/5 | chr7 | 44412926 | ||||||
chr7:44412926
|
C | CAAA | 5 | a0002c0002t0004g0210a0002c0002t0004g0212a0002c0002t0007g0196others(2): Show | 5 | HG00735.hp2 HG01106.hp1 HG01109.hp2 others(2): Show |
intron_variant | MODIFIER | c.643-8346_643-8344d others(5): Show |
NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 3/5 | chr7 | 44412926 | ||||||
chr7:44412926
|
C | CAAAAAAA others(3): Show |
1 | a0002c0002t0010g0201 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.643-8353_643-8344d others(12): Show |
NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 3/5 | chr7 | 44412926 | ||||||
chr7:44412926
|
C | CAAAAAAA others(4): Show |
1 | a0002c0002t0010g0193 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.643-8354_643-8344d others(13): Show |
NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 3/5 | chr7 | 44412926 | ||||||
chr7:44412926
|
CAAAAAAA others(5): Show |
C | 2 | a0001c0001t0001g0160a0001c0001t0001g0168 | 2 | HG01516.hp1 HG02293.hp2 |
intron_variant | MODIFIER | c.643-8355_643-8344d others(14): Show |
NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 3/5 | chr7 | 44412926 | ||||||
chr7:44412926
|
CAAAAAAA others(10): Show |
C | 2 | a0002c0005t0012g0235a0002c0005t0012g0236 | 2 | HG02922.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.643-8360_643-8344d others(19): Show |
NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 3/5 | chr7 | 44412926 | ||||||
chr7:44412932
|
AAAAAAAA others(4): Show |
A | 1 | a0002c0002t0023g0209 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.643-8360_643-8350d others(13): Show |
NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 3/5 | chr7 | 44412932 | ||||||
chr7:44412943
|
G | A | 35 | a0002c0002t0004g0207a0002c0002t0004g0208a0002c0002t0004g0210others(32): Show | 35 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(32): Show |
intron_variant | MODIFIER | c.643-8360C>T | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 3/5 | chr7 | 44412943 | ||||||
chr7:44412951
|
A | AAAG | 6 | a0003c0003t0006g0226a0003c0003t0006g0229a0003c0003t0006g0234others(3): Show | 6 | HG00438.hp1 HG01358.hp2 HG04184.hp2 others(3): Show |
intron_variant | MODIFIER | c.643-8369_643-8368i others(5): Show |
NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 3/5 | chr7 | 44412951 | ||||||
chr7:44412951
|
A | AAG | 11 | a0002c0002t0011g0194a0002c0002t0011g0195a0003c0003t0005g0218others(8): Show | 11 | HG00280.hp1 HG00280.hp2 HG01168.hp2 others(8): Show |
intron_variant | MODIFIER | c.643-8369_643-8368i others(4): Show |
NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 3/5 | chr7 | 44412951 | ||||||
chr7:44412951
|
A | G | 1 | a0002c0002t0021g0217 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.643-8368T>C | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 3/5 | chr7 | 44412951 | ||||||
chr7:44413039
|
G | C | 2 | a0002c0002t0010g0193a0002c0002t0010g0201 | 2 | HG00741.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.643-8456C>G | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 3/5 | chr7 | 44413039 | ||||||
chr7:44413297
|
A | T | 7 | a0001c0001t0001g0023a0001c0001t0001g0028a0001c0001t0001g0034others(4): Show | 7 | HG01993.hp2 HG02293.hp1 NA18941.hp1 others(4): Show |
intron_variant | MODIFIER | c.643-8714T>A | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 3/5 | chr7 | 44413297 | ||||||
chr7:44413407
|
A | C | 19 | a0002c0002t0021g0217a0002c0002t0040g0237a0003c0003t0005g0218others(16): Show | 19 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(16): Show |
intron_variant | MODIFIER | c.643-8824T>G | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 3/5 | chr7 | 44413407 | ||||||
chr7:44413558
|
C | T | 1 | a0001c0001t0001g0117 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.643-8975G>A | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 3/5 | chr7 | 44413558 | ||||||
chr7:44413702
|
T | C | 2 | a0001c0001t0001g0097a0001c0001t0028g0111 | 2 | NA18955.hp1 NA19063.hp2 |
intron_variant | MODIFIER | c.643-9119A>G | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 3/5 | chr7 | 44413702 | ||||||
chr7:44413737
|
T | C | 2 | a0002c0002t0021g0217a0002c0002t0040g0237 | 2 | HG03486.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.643-9154A>G | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 3/5 | chr7 | 44413737 | ||||||
chr7:44413774
|
C | T | 1 | a0001c0001t0001g0037 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.643-9191G>A | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 3/5 | chr7 | 44413774 | ||||||
chr7:44413775
|
G | A | 1 | a0001c0001t0002g0060 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.643-9192C>T | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 3/5 | chr7 | 44413775 | ||||||
chr7:44413928
|
G | A | 31 | a0001c0001t0001g0040a0001c0001t0001g0041a0001c0001t0001g0049others(28): Show | 31 | HG00438.hp2 HG00544.hp1 HG00558.hp1 others(28): Show |
intron_variant | MODIFIER | c.643-9345C>T | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 3/5 | chr7 | 44413928 | ||||||
chr7:44413955
|
T | C | 1 | a0001c0001t0001g0137 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.643-9372A>G | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 3/5 | chr7 | 44413955 | ||||||
chr7:44414089
|
G | C | 1 | a0003c0003t0006g0234 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.643-9506C>G | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 3/5 | chr7 | 44414089 | ||||||
chr7:44414381
|
G | T | 7 | a0002c0002t0007g0196a0002c0002t0007g0197a0002c0002t0007g0198others(4): Show | 7 | HG00741.hp2 HG02486.hp2 HG02622.hp1 others(4): Show |
intron_variant | MODIFIER | c.643-9798C>A | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 3/5 | chr7 | 44414381 | ||||||
chr7:44414462
|
C | T | 2 | a0002c0002t0011g0194a0002c0002t0011g0195 | 2 | HG02486.hp2 HG02622.hp1 |
intron_variant | MODIFIER | c.643-9879G>A | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 3/5 | chr7 | 44414462 | ||||||
chr7:44414508
|
T | G | 3 | a0001c0001t0001g0156a0001c0001t0001g0158a0001c0001t0001g0159 | 3 | HG03834.hp1 HG04204.hp2 NA20905.hp1 |
intron_variant | MODIFIER | c.643-9925A>C | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 3/5 | chr7 | 44414508 | ||||||
chr7:44414626
|
C | T | 17 | a0003c0003t0005g0218a0003c0003t0005g0219a0003c0003t0005g0221others(14): Show | 17 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(14): Show |
intron_variant | MODIFIER | c.643-10043G>A | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 3/5 | chr7 | 44414626 | ||||||
chr7:44414776
|
T | C | 11 | a0002c0002t0004g0207a0002c0002t0004g0208a0002c0002t0004g0210others(8): Show | 11 | HG00735.hp2 HG01070.hp2 HG01071.hp1 others(8): Show |
intron_variant | MODIFIER | c.643-10193A>G | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 3/5 | chr7 | 44414776 | ||||||
chr7:44414892
|
T | A | 1 | a0001c0001t0001g0090 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.643-10309A>T | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 3/5 | chr7 | 44414892 | ||||||
chr7:44414903
|
C | T | 2 | a0002c0002t0011g0194a0002c0002t0011g0195 | 2 | HG02486.hp2 HG02622.hp1 |
intron_variant | MODIFIER | c.643-10320G>A | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 3/5 | chr7 | 44414903 | ||||||
chr7:44415238
|
T | C | 1 | a0001c0001t0001g0119 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.643-10655A>G | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 3/5 | chr7 | 44415238 | ||||||
chr7:44415333
|
A | AAG | 2 | a0002c0002t0021g0217a0002c0002t0040g0237 | 2 | HG03486.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.643-10752_643-1075 others(6): Show |
NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 3/5 | chr7 | 44415333 | ||||||
chr7:44415357
|
T | C | 1 | a0001c0001t0002g0059 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.643-10774A>G | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 3/5 | chr7 | 44415357 | ||||||
chr7:44415428
|
T | C | 1 | a0002c0002t0023g0209 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.643-10845A>G | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 3/5 | chr7 | 44415428 | ||||||
chr7:44415487
|
T | C | 3 | a0002c0002t0007g0196a0002c0002t0007g0197a0002c0002t0007g0198 | 3 | HG03453.hp1 HG03516.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.643-10904A>G | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 3/5 | chr7 | 44415487 | ||||||
chr7:44416043
|
A | G | 7 | a0003c0003t0006g0226a0003c0003t0006g0229a0003c0003t0006g0231others(4): Show | 7 | HG00438.hp1 HG01358.hp2 HG04184.hp2 others(4): Show |
intron_variant | MODIFIER | c.643-11460T>C | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 3/5 | chr7 | 44416043 | ||||||
chr7:44416222
|
T | C | 11 | a0002c0002t0004g0207a0002c0002t0004g0208a0002c0002t0004g0210others(8): Show | 11 | HG00735.hp2 HG01070.hp2 HG01071.hp1 others(8): Show |
intron_variant | MODIFIER | c.642+11349A>G | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 3/5 | chr7 | 44416222 | ||||||
chr7:44416234
|
C | A | 1 | a0002c0002t0040g0237 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.642+11337G>T | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 3/5 | chr7 | 44416234 | ||||||
chr7:44416263
|
C | T | 40 | a0002c0002t0004g0207a0002c0002t0004g0208a0002c0002t0004g0210others(37): Show | 40 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(37): Show |
intron_variant | MODIFIER | c.642+11308G>A | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 3/5 | chr7 | 44416263 | ||||||
chr7:44416327
|
A | G | 19 | a0002c0002t0021g0217a0002c0002t0040g0237a0003c0003t0005g0218others(16): Show | 19 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(16): Show |
intron_variant | MODIFIER | c.642+11244T>C | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 3/5 | chr7 | 44416327 | ||||||
chr7:44416470
|
T | C | 234 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(231): Show | 235 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(232): Show |
intron_variant | MODIFIER | c.642+11101A>G | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 3/5 | chr7 | 44416470 | ||||||
chr7:44416930
|
C | CT | 2 | a0004c0004t0003g0025a0004c0004t0003g0026 | 2 | HG00639.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.642+10640dupA | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 3/5 | chr7 | 44416930 | ||||||
chr7:44417172
|
G | A | 2 | a0001c0001t0003g0043a0001c0001t0003g0063 | 2 | HG02523.hp1 NA19084.hp2 |
intron_variant | MODIFIER | c.642+10399C>T | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 3/5 | chr7 | 44417172 | ||||||
chr7:44417291
|
C | T | 45 | a0002c0002t0004g0207a0002c0002t0004g0208a0002c0002t0004g0210others(42): Show | 45 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(42): Show |
intron_variant | MODIFIER | c.642+10280G>A | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 3/5 | chr7 | 44417291 | ||||||
chr7:44417700
|
C | A | 11 | a0002c0002t0004g0207a0002c0002t0004g0208a0002c0002t0004g0210others(8): Show | 11 | HG00735.hp2 HG01070.hp2 HG01071.hp1 others(8): Show |
intron_variant | MODIFIER | c.642+9871G>T | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 3/5 | chr7 | 44417700 | ||||||
chr7:44417800
|
C | A | 2 | a0001c0001t0002g0058a0001c0001t0002g0178 | 2 | HG02602.hp2 HG04115.hp2 |
intron_variant | MODIFIER | c.642+9771G>T | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 3/5 | chr7 | 44417800 | ||||||
chr7:44417914
|
T | C | 11 | a0001c0001t0001g0036a0001c0001t0001g0037a0001c0001t0001g0038others(8): Show | 11 | HG00639.hp1 HG02109.hp1 HG02145.hp1 others(8): Show |
intron_variant | MODIFIER | c.642+9657A>G | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 3/5 | chr7 | 44417914 | ||||||
chr7:44418065
|
T | C | 2 | a0002c0005t0012g0235a0002c0005t0012g0236 | 2 | HG02922.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.642+9506A>G | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 3/5 | chr7 | 44418065 | ||||||
chr7:44418273
|
C | G | 40 | a0001c0001t0001g0010a0001c0001t0001g0012a0001c0001t0001g0021others(37): Show | 40 | HG00609.hp1 HG00741.hp1 HG01071.hp2 others(37): Show |
intron_variant | MODIFIER | c.642+9298G>C | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 3/5 | chr7 | 44418273 | ||||||
chr7:44418485
|
A | G | 17 | a0003c0003t0005g0218a0003c0003t0005g0219a0003c0003t0005g0221others(14): Show | 17 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(14): Show |
intron_variant | MODIFIER | c.642+9086T>C | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 3/5 | chr7 | 44418485 | ||||||
chr7:44418518
|
T | C | 2 | a0001c0001t0002g0058a0001c0001t0002g0178 | 2 | HG02602.hp2 HG04115.hp2 |
intron_variant | MODIFIER | c.642+9053A>G | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 3/5 | chr7 | 44418518 | ||||||
chr7:44418796
|
C | T | 1 | a0001c0001t0001g0041 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.642+8775G>A | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 3/5 | chr7 | 44418796 | ||||||
chr7:44418875
|
A | G | 29 | a0002c0002t0007g0196a0002c0002t0007g0197a0002c0002t0007g0198others(26): Show | 29 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(26): Show |
intron_variant | MODIFIER | c.642+8696T>C | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 3/5 | chr7 | 44418875 | ||||||
chr7:44419014
|
A | C | 3 | a0002c0002t0007g0196a0002c0002t0007g0197a0002c0002t0007g0198 | 3 | HG03453.hp1 HG03516.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.642+8557T>G | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 3/5 | chr7 | 44419014 | ||||||
chr7:44419224
|
G | A | 1 | a0002c0002t0021g0217 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.642+8347C>T | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 3/5 | chr7 | 44419224 | ||||||
chr7:44419326
|
G | GC | 235 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(232): Show | 236 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(233): Show |
intron_variant | MODIFIER | c.642+8244dupG | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 3/5 | chr7 | 44419326 | ||||||
chr7:44419497
|
GCTAAGGG others(9): Show |
G | 3 | a0002c0002t0008g0204a0002c0002t0008g0205a0002c0002t0008g0206 | 3 | HG02257.hp1 NA18522.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.642+8058_642+8073d others(18): Show |
NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 3/5 | chr7 | 44419497 | ||||||
chr7:44420152
|
C | G | 8 | a0001c0001t0001g0160a0001c0001t0001g0161a0001c0001t0001g0162others(5): Show | 8 | HG00741.hp1 HG01071.hp2 HG01168.hp1 others(5): Show |
intron_variant | MODIFIER | c.642+7419G>C | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 3/5 | chr7 | 44420152 | ||||||
chr7:44420216
|
C | T | 19 | a0002c0002t0021g0217a0002c0002t0040g0237a0003c0003t0005g0218others(16): Show | 19 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(16): Show |
intron_variant | MODIFIER | c.642+7355G>A | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 3/5 | chr7 | 44420216 | ||||||
chr7:44420491
|
T | C | 1 | a0001c0001t0001g0165 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.642+7080A>G | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 3/5 | chr7 | 44420491 | ||||||
chr7:44420546
|
C | T | 3 | a0002c0002t0007g0196a0002c0002t0007g0197a0002c0002t0007g0198 | 3 | HG03453.hp1 HG03516.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.642+7025G>A | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 3/5 | chr7 | 44420546 | ||||||
chr7:44420627
|
G | A | 1 | a0001c0001t0025g0129 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.642+6944C>T | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 3/5 | chr7 | 44420627 | ||||||
chr7:44420782
|
T | C | 3 | a0002c0002t0007g0196a0002c0002t0007g0197a0002c0002t0007g0198 | 3 | HG03453.hp1 HG03516.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.642+6789A>G | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 3/5 | chr7 | 44420782 | ||||||
chr7:44420874
|
G | A | 7 | a0002c0002t0007g0196a0002c0002t0007g0197a0002c0002t0007g0198others(4): Show | 7 | HG00741.hp2 HG02486.hp2 HG02622.hp1 others(4): Show |
intron_variant | MODIFIER | c.642+6697C>T | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 3/5 | chr7 | 44420874 | ||||||
chr7:44420888
|
C | T | 1 | a0001c0001t0001g0136 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.642+6683G>A | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 3/5 | chr7 | 44420888 | ||||||
chr7:44420900
|
A | G | 2 | a0002c0002t0021g0217a0002c0002t0040g0237 | 2 | HG03486.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.642+6671T>C | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 3/5 | chr7 | 44420900 | ||||||
chr7:44421073
|
C | T | 8 | a0003c0003t0005g0218a0003c0003t0005g0219a0003c0003t0005g0221others(5): Show | 8 | HG00099.hp2 HG00280.hp1 HG01168.hp2 others(5): Show |
intron_variant | MODIFIER | c.642+6498G>A | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 3/5 | chr7 | 44421073 | ||||||
chr7:44421088
|
C | T | 2 | a0001c0001t0001g0037a0001c0001t0001g0051 | 2 | HG02486.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.642+6483G>A | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 3/5 | chr7 | 44421088 | ||||||
chr7:44421115
|
C | T | 1 | a0001c0001t0001g0102 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.642+6456G>A | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 3/5 | chr7 | 44421115 | ||||||
chr7:44421266
|
A | G | 19 | a0002c0002t0021g0217a0002c0002t0040g0237a0003c0003t0005g0218others(16): Show | 19 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(16): Show |
intron_variant | MODIFIER | c.642+6305T>C | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 3/5 | chr7 | 44421266 | ||||||
chr7:44421331
|
T | TA | 166 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(163): Show | 167 | HG00099.hp1 HG00323.hp2 HG00544.hp1 others(164): Show |
intron_variant | MODIFIER | c.642+6239dupT | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 3/5 | chr7 | 44421331 | ||||||
chr7:44421331
|
T | TAA | 13 | a0001c0001t0001g0056a0001c0001t0001g0094a0001c0001t0001g0108others(10): Show | 13 | HG00438.hp2 HG01106.hp2 HG02257.hp2 others(10): Show |
intron_variant | MODIFIER | c.642+6238_642+6239d others(4): Show |
NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 3/5 | chr7 | 44421331 | ||||||
chr7:44421331
|
TA | T | 18 | a0002c0002t0021g0217a0002c0002t0023g0209a0002c0002t0040g0237others(15): Show | 18 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(15): Show |
intron_variant | MODIFIER | c.642+6239delT | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 3/5 | chr7 | 44421331 | ||||||
chr7:44421487
|
C | CA | 157 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(154): Show | 158 | HG00099.hp1 HG00323.hp2 HG00544.hp1 others(155): Show |
intron_variant | MODIFIER | c.642+6083dupT | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 3/5 | chr7 | 44421487 | ||||||
chr7:44421487
|
CA | C | 20 | a0001c0001t0002g0189a0002c0002t0021g0217a0002c0005t0012g0235others(17): Show | 20 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(17): Show |
intron_variant | MODIFIER | c.642+6083delT | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 3/5 | chr7 | 44421487 | ||||||
chr7:44421655
|
C | G | 17 | a0003c0003t0005g0218a0003c0003t0005g0219a0003c0003t0005g0221others(14): Show | 17 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(14): Show |
intron_variant | MODIFIER | c.642+5916G>C | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 3/5 | chr7 | 44421655 | ||||||
chr7:44421675
|
T | C | 1 | a0002c0002t0018g0200 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.642+5896A>G | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 3/5 | chr7 | 44421675 | ||||||
chr7:44421759
|
G | A | 1 | a0001c0001t0002g0011 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.642+5812C>T | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 3/5 | chr7 | 44421759 | ||||||
chr7:44421919
|
G | T | 1 | a0001c0001t0001g0150 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.642+5652C>A | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 3/5 | chr7 | 44421919 | ||||||
chr7:44422278
|
T | C | 1 | a0005c0007t0001g0192 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.642+5293A>G | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 3/5 | chr7 | 44422278 | ||||||
chr7:44422350
|
G | C | 1 | a0002c0002t0040g0237 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.642+5221C>G | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 3/5 | chr7 | 44422350 | ||||||
chr7:44422679
|
G | A | 3 | a0002c0002t0007g0196a0002c0002t0007g0197a0002c0002t0007g0198 | 3 | HG03453.hp1 HG03516.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.642+4892C>T | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 3/5 | chr7 | 44422679 | ||||||
chr7:44422714
|
G | A | 1 | a0002c0002t0040g0237 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.642+4857C>T | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 3/5 | chr7 | 44422714 | ||||||
chr7:44422944
|
C | T | 1 | a0001c0001t0002g0052 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.642+4627G>A | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 3/5 | chr7 | 44422944 | ||||||
chr7:44423011
|
C | G | 17 | a0003c0003t0005g0218a0003c0003t0005g0219a0003c0003t0005g0221others(14): Show | 17 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(14): Show |
intron_variant | MODIFIER | c.642+4560G>C | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 3/5 | chr7 | 44423011 | ||||||
chr7:44423257
|
C | T | 1 | a0002c0002t0040g0237 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.642+4314G>A | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 3/5 | chr7 | 44423257 | ||||||
chr7:44423326
|
C | T | 1 | a0001c0001t0001g0001 | 2 | HG01516.hp2 HG01517.hp2 |
intron_variant | MODIFIER | c.642+4245G>A | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 3/5 | chr7 | 44423326 | ||||||
chr7:44423336
|
G | A | 1 | a0002c0002t0023g0209 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.642+4235C>T | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 3/5 | chr7 | 44423336 | ||||||
chr7:44423377
|
G | T | 1 | a0001c0001t0002g0189 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.642+4194C>A | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 3/5 | chr7 | 44423377 | ||||||
chr7:44423532
|
C | G | 1 | a0001c0001t0001g0021 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.642+4039G>C | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 3/5 | chr7 | 44423532 | ||||||
chr7:44423696
|
T | G | 1 | a0001c0001t0001g0012 | 1 | NA18957.hp2 | intron_variant | MODIFIER | c.642+3875A>C | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 3/5 | chr7 | 44423696 | ||||||
chr7:44423734
|
C | T | 17 | a0003c0003t0005g0218a0003c0003t0005g0219a0003c0003t0005g0221others(14): Show | 17 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(14): Show |
intron_variant | MODIFIER | c.642+3837G>A | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 3/5 | chr7 | 44423734 | ||||||
chr7:44424054
|
C | T | 19 | a0002c0002t0021g0217a0002c0002t0040g0237a0003c0003t0005g0218others(16): Show | 19 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(16): Show |
intron_variant | MODIFIER | c.642+3517G>A | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 3/5 | chr7 | 44424054 | ||||||
chr7:44424224
|
C | T | 2 | a0002c0002t0010g0193a0002c0002t0010g0201 | 2 | HG00741.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.642+3347G>A | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 3/5 | chr7 | 44424224 | ||||||
chr7:44424492
|
C | T | 1 | a0001c0001t0001g0035 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.642+3079G>A | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 3/5 | chr7 | 44424492 | ||||||
chr7:44424532
|
G | A | 29 | a0002c0002t0007g0196a0002c0002t0007g0197a0002c0002t0007g0198others(26): Show | 29 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(26): Show |
intron_variant | MODIFIER | c.642+3039C>T | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 3/5 | chr7 | 44424532 | ||||||
chr7:44424549
|
T | A | 29 | a0002c0002t0007g0196a0002c0002t0007g0197a0002c0002t0007g0198others(26): Show | 29 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(26): Show |
intron_variant | MODIFIER | c.642+3022A>T | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 3/5 | chr7 | 44424549 | ||||||
chr7:44424553
|
T | G | 29 | a0002c0002t0007g0196a0002c0002t0007g0197a0002c0002t0007g0198others(26): Show | 29 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(26): Show |
intron_variant | MODIFIER | c.642+3018A>C | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 3/5 | chr7 | 44424553 | ||||||
chr7:44424620
|
T | C | 1 | a0002c0002t0023g0209 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.642+2951A>G | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 3/5 | chr7 | 44424620 | ||||||
chr7:44424684
|
T | C | 2 | a0002c0002t0007g0196a0002c0002t0007g0197 | 2 | HG03453.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.642+2887A>G | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 3/5 | chr7 | 44424684 | ||||||
chr7:44424963
|
T | C | 2 | a0002c0005t0012g0235a0002c0005t0012g0236 | 2 | HG02922.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.642+2608A>G | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 3/5 | chr7 | 44424963 | ||||||
chr7:44425216
|
G | A | 1 | a0001c0001t0001g0035 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.642+2355C>T | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 3/5 | chr7 | 44425216 | ||||||
chr7:44425395
|
G | A | 3 | a0002c0002t0008g0204a0002c0002t0008g0205a0002c0002t0008g0206 | 3 | HG02257.hp1 NA18522.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.642+2176C>T | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 3/5 | chr7 | 44425395 | ||||||
chr7:44425523
|
G | T | 1 | a0001c0001t0026g0186 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.642+2048C>A | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 3/5 | chr7 | 44425523 | ||||||
chr7:44425525
|
T | C | 19 | a0002c0002t0021g0217a0002c0002t0040g0237a0003c0003t0005g0218others(16): Show | 19 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(16): Show |
intron_variant | MODIFIER | c.642+2046A>G | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 3/5 | chr7 | 44425525 | ||||||
chr7:44425666
|
C | A | 1 | a0002c0002t0040g0237 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.642+1905G>T | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 3/5 | chr7 | 44425666 | ||||||
chr7:44425669
|
G | T | 1 | a0002c0002t0040g0237 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.642+1902C>A | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 3/5 | chr7 | 44425669 | ||||||
chr7:44425779
|
T | C | 2 | a0003c0003t0005g0224a0003c0003t0005g0233 | 2 | HG00280.hp1 NA20805.hp2 |
intron_variant | MODIFIER | c.642+1792A>G | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 3/5 | chr7 | 44425779 | ||||||
chr7:44425817
|
G | A | 11 | a0002c0002t0004g0207a0002c0002t0004g0208a0002c0002t0004g0210others(8): Show | 11 | HG00735.hp2 HG01070.hp2 HG01071.hp1 others(8): Show |
intron_variant | MODIFIER | c.642+1754C>T | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 3/5 | chr7 | 44425817 | ||||||
chr7:44425849
|
G | A | 1 | a0003c0003t0009g0228 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.642+1722C>T | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 3/5 | chr7 | 44425849 | ||||||
chr7:44426507
|
G | C | 1 | a0002c0002t0040g0237 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.642+1064C>G | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 3/5 | chr7 | 44426507 | ||||||
chr7:44426518
|
C | T | 3 | a0002c0002t0008g0204a0002c0002t0008g0205a0002c0002t0008g0206 | 3 | HG02257.hp1 NA18522.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.642+1053G>A | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 3/5 | chr7 | 44426518 | ||||||
chr7:44426522
|
C | T | 2 | a0002c0002t0011g0194a0002c0002t0011g0195 | 2 | HG02486.hp2 HG02622.hp1 |
intron_variant | MODIFIER | c.642+1049G>A | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 3/5 | chr7 | 44426522 | ||||||
chr7:44426553
|
T | C | 1 | a0002c0002t0040g0237 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.642+1018A>G | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 3/5 | chr7 | 44426553 | ||||||
chr7:44426572
|
G | A | 17 | a0003c0003t0005g0218a0003c0003t0005g0219a0003c0003t0005g0221others(14): Show | 17 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(14): Show |
intron_variant | MODIFIER | c.642+999C>T | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 3/5 | chr7 | 44426572 | ||||||
chr7:44426613
|
A | G | 19 | a0002c0002t0021g0217a0002c0002t0040g0237a0003c0003t0005g0218others(16): Show | 19 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(16): Show |
intron_variant | MODIFIER | c.642+958T>C | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 3/5 | chr7 | 44426613 | ||||||
chr7:44426772
|
G | C | 1 | a0001c0001t0037g0081 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.642+799C>G | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 3/5 | chr7 | 44426772 | ||||||
chr7:44426779
|
G | A | 1 | a0002c0002t0023g0209 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.642+792C>T | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 3/5 | chr7 | 44426779 | ||||||
chr7:44426795
|
C | CA | 6 | a0001c0001t0001g0046a0001c0001t0001g0136a0001c0001t0001g0140others(3): Show | 6 | HG01981.hp1 HG02572.hp2 HG03130.hp1 others(3): Show |
intron_variant | MODIFIER | c.642+775dupT | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 3/5 | chr7 | 44426795 | ||||||
chr7:44426868
|
T | A | 7 | a0003c0003t0006g0226a0003c0003t0006g0229a0003c0003t0006g0231others(4): Show | 7 | HG00438.hp1 HG01358.hp2 HG04184.hp2 others(4): Show |
intron_variant | MODIFIER | c.642+703A>T | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 3/5 | chr7 | 44426868 | ||||||
chr7:44427130
|
T | G | 89 | a0001c0001t0001g0001a0001c0001t0001g0017a0001c0001t0001g0018others(86): Show | 90 | HG00099.hp1 HG00323.hp2 HG00438.hp2 others(87): Show |
intron_variant | MODIFIER | c.642+441A>C | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 3/5 | chr7 | 44427130 | ||||||
chr7:44427161
|
C | A | 1 | a0001c0001t0001g0085 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.642+410G>T | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 3/5 | chr7 | 44427161 | ||||||
chr7:44427277
|
A | G | 43 | a0002c0002t0004g0207a0002c0002t0004g0208a0002c0002t0004g0210others(40): Show | 43 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(40): Show |
intron_variant | MODIFIER | c.642+294T>C | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 3/5 | chr7 | 44427277 | ||||||
chr7:44427534
|
G | A | 2 | a0002c0002t0011g0194a0002c0002t0011g0195 | 2 | HG02486.hp2 HG02622.hp1 |
intron_variant | MODIFIER | c.642+37C>T | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 3/5 | chr7 | 44427534 | ||||||
chr7:44427798
|
C | A | 3 | a0002c0002t0008g0204a0002c0002t0008g0205a0002c0002t0008g0206 | 3 | HG02257.hp1 NA18522.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.510-95G>T | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 2/5 | chr7 | 44427798 | ||||||
chr7:44427833
|
C | T | 11 | a0002c0002t0004g0207a0002c0002t0004g0208a0002c0002t0004g0210others(8): Show | 11 | HG00735.hp2 HG01070.hp2 HG01071.hp1 others(8): Show |
intron_variant | MODIFIER | c.510-130G>A | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 2/5 | chr7 | 44427833 | ||||||
chr7:44428116
|
C | G | 2 | a0001c0001t0001g0126a0001c0001t0001g0128 | 2 | HG00642.hp2 HG01169.hp2 |
intron_variant | MODIFIER | c.510-413G>C | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 2/5 | chr7 | 44428116 | ||||||
chr7:44428123
|
T | TA | 20 | a0001c0001t0001g0036a0001c0001t0001g0094a0001c0001t0002g0011others(17): Show | 20 | HG00323.hp1 HG00741.hp2 HG01106.hp1 others(17): Show |
intron_variant | MODIFIER | c.510-421dupT | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 2/5 | chr7 | 44428123 | ||||||
chr7:44428123
|
TA | T | 35 | a0001c0001t0001g0017a0001c0001t0001g0018a0001c0001t0001g0019others(32): Show | 35 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(32): Show |
intron_variant | MODIFIER | c.510-421delT | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 2/5 | chr7 | 44428123 | ||||||
chr7:44428334
|
G | A | 1 | a0002c0002t0040g0237 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.510-631C>T | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 2/5 | chr7 | 44428334 | ||||||
chr7:44428363
|
G | A | 1 | a0002c0002t0007g0198 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.510-660C>T | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 2/5 | chr7 | 44428363 | ||||||
chr7:44428456
|
G | C | 1 | a0002c0002t0023g0209 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.510-753C>G | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 2/5 | chr7 | 44428456 | ||||||
chr7:44428593
|
T | C | 1 | a0002c0002t0040g0237 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.510-890A>G | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 2/5 | chr7 | 44428593 | ||||||
chr7:44428722
|
C | T | 1 | a0002c0002t0040g0237 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.510-1019G>A | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 2/5 | chr7 | 44428722 | ||||||
chr7:44428723
|
C | T | 1 | a0002c0002t0040g0237 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.510-1020G>A | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 2/5 | chr7 | 44428723 | ||||||
chr7:44428724
|
A | T | 1 | a0002c0002t0040g0237 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.510-1021T>A | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 2/5 | chr7 | 44428724 | ||||||
chr7:44428726
|
A | T | 1 | a0002c0002t0040g0237 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.510-1023T>A | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 2/5 | chr7 | 44428726 | ||||||
chr7:44428727
|
A | T | 1 | a0002c0002t0040g0237 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.510-1024T>A | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 2/5 | chr7 | 44428727 | ||||||
chr7:44428729
|
A | T | 1 | a0002c0002t0040g0237 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.510-1026T>A | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 2/5 | chr7 | 44428729 | ||||||
chr7:44428731
|
G | A | 1 | a0002c0002t0040g0237 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.510-1028C>T | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 2/5 | chr7 | 44428731 | ||||||
chr7:44428732
|
TAACAATG others(36): Show |
T | 1 | a0002c0002t0040g0237 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.510-1072_510-1030d others(45): Show |
NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 2/5 | chr7 | 44428732 | ||||||
chr7:44428777
|
G | T | 1 | a0002c0002t0040g0237 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.510-1074C>A | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 2/5 | chr7 | 44428777 | ||||||
chr7:44428779
|
C | A | 1 | a0002c0002t0040g0237 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.510-1076G>T | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 2/5 | chr7 | 44428779 | ||||||
chr7:44428780
|
C | T | 1 | a0002c0002t0040g0237 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.510-1077G>A | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 2/5 | chr7 | 44428780 | ||||||
chr7:44428787
|
G | T | 1 | a0002c0002t0040g0237 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.510-1084C>A | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 2/5 | chr7 | 44428787 | ||||||
chr7:44428789
|
G | A | 1 | a0002c0002t0040g0237 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.510-1086C>T | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 2/5 | chr7 | 44428789 | ||||||
chr7:44428792
|
C | T | 1 | a0002c0002t0040g0237 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.510-1089G>A | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 2/5 | chr7 | 44428792 | ||||||
chr7:44428797
|
G | C | 1 | a0002c0002t0040g0237 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.510-1094C>G | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 2/5 | chr7 | 44428797 | ||||||
chr7:44428963
|
A | G | 1 | a0001c0001t0001g0074 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.510-1260T>C | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 2/5 | chr7 | 44428963 | ||||||
chr7:44429413
|
T | C | 1 | a0001c0001t0001g0116 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.510-1710A>G | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 2/5 | chr7 | 44429413 | ||||||
chr7:44429426
|
G | A | 2 | a0001c0001t0001g0077a0001c0001t0001g0115 | 2 | HG00558.hp1 HG00673.hp1 |
intron_variant | MODIFIER | c.510-1723C>T | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 2/5 | chr7 | 44429426 | ||||||
chr7:44429534
|
C | T | 1 | a0001c0001t0001g0115 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.510-1831G>A | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 2/5 | chr7 | 44429534 | ||||||
chr7:44429689
|
A | T | 1 | a0002c0002t0021g0217 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.510-1986T>A | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 2/5 | chr7 | 44429689 | ||||||
chr7:44429700
|
G | A | 1 | a0001c0001t0017g0068 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.510-1997C>T | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 2/5 | chr7 | 44429700 | ||||||
chr7:44430062
|
C | T | 1 | a0002c0002t0004g0207 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.510-2359G>A | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 2/5 | chr7 | 44430062 | ||||||
chr7:44430131
|
T | C | 2 | a0002c0005t0012g0235a0002c0005t0012g0236 | 2 | HG02922.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.510-2428A>G | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 2/5 | chr7 | 44430131 | ||||||
chr7:44430151
|
T | C | 3 | a0001c0001t0001g0147a0001c0001t0001g0182a0001c0006t0001g0149 | 3 | NA18965.hp1 NA18989.hp1 NA19074.hp1 |
intron_variant | MODIFIER | c.510-2448A>G | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 2/5 | chr7 | 44430151 | ||||||
chr7:44430394
|
T | C | 1 | a0002c0002t0021g0217 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.510-2691A>G | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 2/5 | chr7 | 44430394 | ||||||
chr7:44430481
|
C | T | 19 | a0002c0002t0021g0217a0002c0002t0040g0237a0003c0003t0005g0218others(16): Show | 19 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(16): Show |
intron_variant | MODIFIER | c.510-2778G>A | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 2/5 | chr7 | 44430481 | ||||||
chr7:44430551
|
T | TAC | 2 | a0002c0002t0004g0212a0003c0003t0019g0230 | 2 | HG00280.hp2 HG00735.hp2 |
intron_variant | MODIFIER | c.510-2850_510-2849d others(4): Show |
NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 2/5 | chr7 | 44430551 | ||||||
chr7:44430551
|
TACCCACA others(5): Show |
T | 2 | a0002c0002t0007g0196a0002c0002t0007g0197 | 2 | HG03453.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.510-2860_510-2849d others(14): Show |
NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 2/5 | chr7 | 44430551 | ||||||
chr7:44430551
|
TACCCACA others(9): Show |
T | 1 | a0002c0002t0023g0209 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.510-2864_510-2849d others(18): Show |
NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 2/5 | chr7 | 44430551 | ||||||
chr7:44430552
|
ACC | A | 5 | a0002c0002t0004g0207a0002c0002t0004g0208a0002c0002t0004g0211others(2): Show | 5 | HG02683.hp2 HG02922.hp2 HG03579.hp1 others(2): Show |
intron_variant | MODIFIER | c.510-2851_510-2850d others(4): Show |
NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 2/5 | chr7 | 44430552 | ||||||
chr7:44430554
|
C | A | 6 | a0002c0002t0004g0212a0002c0002t0007g0198a0002c0002t0010g0193others(3): Show | 6 | HG00280.hp2 HG00735.hp2 HG00741.hp2 others(3): Show |
intron_variant | MODIFIER | c.510-2851G>T | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 2/5 | chr7 | 44430554 | ||||||
chr7:44430554
|
C | CCA | 7 | a0001c0001t0030g0180a0002c0002t0008g0205a0003c0003t0006g0226others(4): Show | 7 | HG00438.hp1 HG01358.hp2 HG01496.hp2 others(4): Show |
intron_variant | MODIFIER | c.510-2853_510-2852d others(4): Show |
NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 2/5 | chr7 | 44430554 | ||||||
chr7:44430554
|
C | CCACA | 7 | a0002c0002t0004g0210a0002c0002t0008g0204a0002c0002t0008g0206others(4): Show | 7 | HG01106.hp1 HG02257.hp1 HG02280.hp2 others(4): Show |
intron_variant | MODIFIER | c.510-2855_510-2852d others(6): Show |
NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 2/5 | chr7 | 44430554 | ||||||
chr7:44430558
|
ACACACAC others(5): Show |
A | 1 | a0002c0002t0021g0217 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.510-2867_510-2856d others(14): Show |
NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 2/5 | chr7 | 44430558 | ||||||
chr7:44430560
|
ACACACAC others(3): Show |
A | 3 | a0002c0002t0011g0194a0002c0002t0011g0195a0002c0002t0040g0237 | 3 | HG02486.hp2 HG02622.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.510-2867_510-2858d others(12): Show |
NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 2/5 | chr7 | 44430560 | ||||||
chr7:44430562
|
ACACACAC others(1): Show |
A | 2 | a0003c0003t0005g0218a0003c0003t0005g0219 | 2 | HG03491.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.510-2867_510-2860d others(10): Show |
NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 2/5 | chr7 | 44430562 | ||||||
chr7:44430566
|
ACACT | A | 2 | a0003c0003t0005g0221a0003c0003t0005g0225 | 2 | HG00099.hp2 HG01168.hp2 |
intron_variant | MODIFIER | c.510-2867_510-2864d others(6): Show |
NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 2/5 | chr7 | 44430566 | ||||||
chr7:44430568
|
ACT | A | 4 | a0002c0002t0004g0213a0002c0002t0004g0214a0002c0002t0004g0216others(1): Show | 4 | HG00280.hp1 HG01070.hp2 HG01071.hp1 others(1): Show |
intron_variant | MODIFIER | c.510-2867_510-2866d others(4): Show |
NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 2/5 | chr7 | 44430568 | ||||||
chr7:44430570
|
T | A | 32 | a0002c0002t0004g0207a0002c0002t0004g0208a0002c0002t0004g0210others(29): Show | 32 | HG00280.hp2 HG00438.hp1 HG00735.hp2 others(29): Show |
intron_variant | MODIFIER | c.510-2867A>T | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 2/5 | chr7 | 44430570 | ||||||
chr7:44430570
|
T | TCA | 20 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(17): Show | 20 | HG01109.hp1 HG01257.hp1 HG01515.hp1 others(17): Show |
intron_variant | MODIFIER | c.510-2869_510-2868d others(4): Show |
NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 2/5 | chr7 | 44430570 | ||||||
chr7:44430570
|
T | TCACA | 3 | a0001c0001t0001g0118a0001c0001t0001g0179a0001c0001t0002g0076 | 3 | HG01358.hp1 HG02738.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.510-2871_510-2868d others(6): Show |
NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 2/5 | chr7 | 44430570 | ||||||
chr7:44430570
|
TCA | T | 8 | a0001c0001t0001g0057a0001c0001t0001g0075a0001c0001t0001g0101others(5): Show | 8 | HG01943.hp1 HG03209.hp2 HG03453.hp2 others(5): Show |
intron_variant | MODIFIER | c.510-2869_510-2868d others(4): Show |
NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 2/5 | chr7 | 44430570 | ||||||
chr7:44430570
|
TCACA | T | 6 | a0001c0001t0001g0054a0001c0001t0001g0056a0001c0001t0001g0117others(3): Show | 6 | HG02257.hp2 HG02572.hp2 HG02602.hp2 others(3): Show |
intron_variant | MODIFIER | c.510-2871_510-2868d others(6): Show |
NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 2/5 | chr7 | 44430570 | ||||||
chr7:44430570
|
TCACACAC others(1): Show |
T | 3 | a0001c0001t0001g0094a0001c0001t0001g0095a0001c0001t0001g0100 | 3 | HG03130.hp2 HG03516.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.510-2875_510-2868d others(10): Show |
NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 2/5 | chr7 | 44430570 | ||||||
chr7:44430604
|
A | AC | 2 | a0001c0001t0001g0010a0001c0001t0001g0148 | 2 | NA18955.hp2 NA18975.hp1 |
intron_variant | MODIFIER | c.510-2902_510-2901i others(3): Show |
NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 2/5 | chr7 | 44430604 | ||||||
chr7:44430605
|
A | C | 2 | a0002c0005t0012g0235a0002c0005t0012g0236 | 2 | HG02922.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.510-2902T>G | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 2/5 | chr7 | 44430605 | ||||||
chr7:44430717
|
C | T | 2 | a0001c0001t0002g0099a0001c0001t0014g0013 | 2 | HG00673.hp2 HG01928.hp1 |
intron_variant | MODIFIER | c.510-3014G>A | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 2/5 | chr7 | 44430717 | ||||||
chr7:44430742
|
C | T | 1 | a0001c0001t0001g0152 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.510-3039G>A | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 2/5 | chr7 | 44430742 | ||||||
chr7:44430764
|
T | C | 40 | a0002c0002t0004g0207a0002c0002t0004g0208a0002c0002t0004g0210others(37): Show | 40 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(37): Show |
intron_variant | MODIFIER | c.510-3061A>G | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 2/5 | chr7 | 44430764 | ||||||
chr7:44430938
|
C | T | 1 | a0001c0001t0036g0144 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.510-3235G>A | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 2/5 | chr7 | 44430938 | ||||||
chr7:44430980
|
A | G | 3 | a0002c0002t0021g0217a0002c0002t0023g0209a0002c0002t0040g0237 | 3 | HG03130.hp1 HG03486.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.510-3277T>C | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 2/5 | chr7 | 44430980 | ||||||
chr7:44431020
|
A | G | 17 | a0003c0003t0005g0218a0003c0003t0005g0219a0003c0003t0005g0221others(14): Show | 17 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(14): Show |
intron_variant | MODIFIER | c.510-3317T>C | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 2/5 | chr7 | 44431020 | ||||||
chr7:44431181
|
C | T | 3 | a0001c0001t0001g0163a0001c0001t0001g0169a0001c0001t0001g0170 | 3 | HG01168.hp1 HG01169.hp1 HG01256.hp2 |
intron_variant | MODIFIER | c.510-3478G>A | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 2/5 | chr7 | 44431181 | ||||||
chr7:44431215
|
G | A | 1 | a0002c0002t0004g0208 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.510-3512C>T | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 2/5 | chr7 | 44431215 | ||||||
chr7:44431249
|
G | A | 2 | a0001c0001t0001g0187a0001c0001t0001g0188 | 2 | HG01943.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.510-3546C>T | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 2/5 | chr7 | 44431249 | ||||||
chr7:44431458
|
C | A | 1 | a0001c0001t0001g0074 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.510-3755G>T | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 2/5 | chr7 | 44431458 | ||||||
chr7:44431545
|
C | G | 11 | a0001c0001t0001g0049a0001c0001t0001g0093a0001c0001t0001g0098others(8): Show | 11 | HG00438.hp2 HG01496.hp1 HG01952.hp2 others(8): Show |
intron_variant | MODIFIER | c.510-3842G>C | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 2/5 | chr7 | 44431545 | ||||||
chr7:44431653
|
G | C | 1 | a0002c0002t0040g0237 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.510-3950C>G | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 2/5 | chr7 | 44431653 | ||||||
chr7:44431668
|
C | CT | 12 | a0001c0001t0001g0112a0001c0001t0001g0119a0001c0001t0001g0157others(9): Show | 12 | HG00735.hp2 HG01070.hp2 HG01071.hp1 others(9): Show |
intron_variant | MODIFIER | c.510-3966dupA | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 2/5 | chr7 | 44431668 | ||||||
chr7:44431668
|
C | CTT | 17 | a0002c0002t0004g0210a0003c0003t0005g0218a0003c0003t0005g0219others(14): Show | 17 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(14): Show |
intron_variant | MODIFIER | c.510-3967_510-3966d others(4): Show |
NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 2/5 | chr7 | 44431668 | ||||||
chr7:44431668
|
CT | C | 15 | a0001c0001t0001g0101a0001c0001t0001g0154a0001c0001t0002g0061others(12): Show | 15 | HG00741.hp2 HG01943.hp1 HG02280.hp2 others(12): Show |
intron_variant | MODIFIER | c.510-3966delA | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 2/5 | chr7 | 44431668 | ||||||
chr7:44431759
|
A | G | 40 | a0002c0002t0004g0207a0002c0002t0004g0208a0002c0002t0004g0210others(37): Show | 40 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(37): Show |
intron_variant | MODIFIER | c.510-4056T>C | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 2/5 | chr7 | 44431759 | ||||||
chr7:44431842
|
T | C | 33 | a0001c0001t0001g0007a0001c0001t0001g0040a0001c0001t0001g0041others(30): Show | 33 | HG00438.hp2 HG00544.hp1 HG00558.hp1 others(30): Show |
intron_variant | MODIFIER | c.510-4139A>G | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 2/5 | chr7 | 44431842 | ||||||
chr7:44431962
|
G | C | 3 | a0001c0001t0001g0049a0001c0001t0001g0098a0001c0001t0001g0108 | 3 | NA18960.hp1 NA18965.hp2 NA18989.hp2 |
intron_variant | MODIFIER | c.510-4259C>G | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 2/5 | chr7 | 44431962 | ||||||
chr7:44432098
|
C | T | 2 | a0002c0005t0012g0235a0002c0005t0012g0236 | 2 | HG02922.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.510-4395G>A | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 2/5 | chr7 | 44432098 | ||||||
chr7:44432214
|
T | C | 19 | a0002c0002t0021g0217a0002c0002t0040g0237a0003c0003t0005g0218others(16): Show | 19 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(16): Show |
intron_variant | MODIFIER | c.510-4511A>G | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 2/5 | chr7 | 44432214 | ||||||
chr7:44432215
|
A | G | 1 | a0001c0001t0001g0024 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.510-4512T>C | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 2/5 | chr7 | 44432215 | ||||||
chr7:44432354
|
G | A | 1 | a0001c0001t0026g0186 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.510-4651C>T | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 2/5 | chr7 | 44432354 | ||||||
chr7:44432505
|
C | T | 2 | a0002c0005t0012g0235a0002c0005t0012g0236 | 2 | HG02922.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.510-4802G>A | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 2/5 | chr7 | 44432505 | ||||||
chr7:44432533
|
G | A | 1 | a0001c0001t0001g0119 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.510-4830C>T | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 2/5 | chr7 | 44432533 | ||||||
chr7:44432592
|
G | A | 1 | a0002c0002t0023g0209 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.510-4889C>T | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 2/5 | chr7 | 44432592 | ||||||
chr7:44432619
|
C | T | 1 | a0002c0002t0004g0208 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.510-4916G>A | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 2/5 | chr7 | 44432619 | ||||||
chr7:44432802
|
T | C | 2 | a0001c0001t0001g0087a0001c0001t0001g0157 | 2 | HG03239.hp2 HG03710.hp2 |
intron_variant | MODIFIER | c.510-5099A>G | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 2/5 | chr7 | 44432802 | ||||||
chr7:44433262
|
A | ATG | 14 | a0001c0001t0001g0037a0001c0001t0001g0038a0001c0001t0001g0045others(11): Show | 14 | HG00099.hp2 HG00280.hp1 HG01168.hp2 others(11): Show |
intron_variant | MODIFIER | c.510-5561_510-5560d others(4): Show |
NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 2/5 | chr7 | 44433262 | ||||||
chr7:44433354
|
C | T | 2 | a0001c0001t0001g0094a0001c0001t0001g0095 | 2 | HG03516.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.510-5651G>A | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 2/5 | chr7 | 44433354 | ||||||
chr7:44433398
|
G | A | 1 | a0001c0001t0001g0017 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.510-5695C>T | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 2/5 | chr7 | 44433398 | ||||||
chr7:44433453
|
T | C | 2 | a0001c0001t0001g0022a0001c0001t0001g0023 | 2 | NA18941.hp2 NA19003.hp2 |
intron_variant | MODIFIER | c.510-5750A>G | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 2/5 | chr7 | 44433453 | ||||||
chr7:44433514
|
A | AGT | 3 | a0001c0001t0001g0010a0002c0002t0010g0193a0002c0002t0010g0201 | 3 | HG00741.hp2 HG03139.hp1 NA18975.hp1 |
intron_variant | MODIFIER | c.510-5813_510-5812d others(4): Show |
NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 2/5 | chr7 | 44433514 | ||||||
chr7:44433598
|
G | A | 1 | a0001c0001t0001g0140 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.510-5895C>T | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 2/5 | chr7 | 44433598 | ||||||
chr7:44433600
|
A | G | 27 | a0002c0002t0007g0196a0002c0002t0007g0197a0002c0002t0007g0198others(24): Show | 27 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(24): Show |
intron_variant | MODIFIER | c.510-5897T>C | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 2/5 | chr7 | 44433600 | ||||||
chr7:44433608
|
T | C | 2 | a0002c0005t0012g0235a0002c0005t0012g0236 | 2 | HG02922.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.510-5905A>G | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 2/5 | chr7 | 44433608 | ||||||
chr7:44433850
|
C | A | 2 | a0002c0002t0018g0199a0002c0002t0018g0200 | 2 | HG02895.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.510-6147G>T | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 2/5 | chr7 | 44433850 | ||||||
chr7:44434020
|
G | A | 2 | a0002c0002t0021g0217a0002c0002t0040g0237 | 2 | HG03486.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.510-6317C>T | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 2/5 | chr7 | 44434020 | ||||||
chr7:44434220
|
TGCCTGGA others(57): Show |
T | 1 | a0005c0007t0001g0192 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.510-6581_510-6518d others(66): Show |
NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 2/5 | chr7 | 44434220 | ||||||
chr7:44434265
|
A | G | 1 | a0001c0001t0026g0186 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.510-6562T>C | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 2/5 | chr7 | 44434265 | ||||||
chr7:44434421
|
G | A | 2 | a0002c0002t0021g0217a0002c0002t0040g0237 | 2 | HG03486.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.510-6718C>T | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 2/5 | chr7 | 44434421 | ||||||
chr7:44434517
|
T | C | 2 | a0001c0001t0001g0034a0001c0001t0003g0032 | 2 | NA18948.hp2 NA18971.hp2 |
intron_variant | MODIFIER | c.510-6814A>G | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 2/5 | chr7 | 44434517 | ||||||
chr7:44434700
|
A | G | 1 | a0001c0001t0001g0185 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.510-6997T>C | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 2/5 | chr7 | 44434700 | ||||||
chr7:44435021
|
G | C | 1 | a0002c0002t0021g0217 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.510-7318C>G | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 2/5 | chr7 | 44435021 | ||||||
chr7:44435023
|
G | A | 1 | a0002c0002t0021g0217 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.510-7320C>T | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 2/5 | chr7 | 44435023 | ||||||
chr7:44435049
|
T | G | 19 | a0002c0002t0021g0217a0002c0002t0040g0237a0003c0003t0005g0218others(16): Show | 19 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(16): Show |
intron_variant | MODIFIER | c.510-7346A>C | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 2/5 | chr7 | 44435049 | ||||||
chr7:44435072
|
T | G | 1 | a0002c0002t0004g0212 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.510-7369A>C | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 2/5 | chr7 | 44435072 | ||||||
chr7:44435092
|
CTTT | C | 17 | a0003c0003t0005g0218a0003c0003t0005g0219a0003c0003t0005g0221others(14): Show | 17 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(14): Show |
intron_variant | MODIFIER | c.510-7392_510-7390d others(5): Show |
NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 2/5 | chr7 | 44435092 | ||||||
chr7:44435278
|
A | G | 2 | a0002c0002t0004g0213a0002c0002t0004g0216 | 2 | HG01070.hp2 HG01071.hp1 |
intron_variant | MODIFIER | c.510-7575T>C | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 2/5 | chr7 | 44435278 | ||||||
chr7:44435310
|
C | T | 2 | a0002c0005t0012g0235a0002c0005t0012g0236 | 2 | HG02922.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.510-7607G>A | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 2/5 | chr7 | 44435310 | ||||||
chr7:44435324
|
G | A | 3 | a0001c0001t0001g0035a0002c0005t0012g0235a0002c0005t0012g0236 | 3 | HG02922.hp2 HG03579.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.510-7621C>T | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 2/5 | chr7 | 44435324 | ||||||
chr7:44435363
|
G | T | 3 | a0002c0002t0007g0196a0002c0002t0007g0197a0002c0002t0007g0198 | 3 | HG03453.hp1 HG03516.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.510-7660C>A | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 2/5 | chr7 | 44435363 | ||||||
chr7:44435668
|
C | G | 5 | a0002c0002t0007g0196a0002c0002t0007g0197a0002c0002t0007g0198others(2): Show | 5 | HG02486.hp2 HG02622.hp1 HG03453.hp1 others(2): Show |
intron_variant | MODIFIER | c.510-7965G>C | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 2/5 | chr7 | 44435668 | ||||||
chr7:44435909
|
G | C | 2 | a0001c0001t0001g0179a0001c0001t0037g0081 | 2 | HG02738.hp2 NA20905.hp2 |
intron_variant | MODIFIER | c.510-8206C>G | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 2/5 | chr7 | 44435909 | ||||||
chr7:44436151
|
C | T | 19 | a0002c0002t0021g0217a0002c0002t0040g0237a0003c0003t0005g0218others(16): Show | 19 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(16): Show |
intron_variant | MODIFIER | c.510-8448G>A | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 2/5 | chr7 | 44436151 | ||||||
chr7:44436332
|
C | T | 17 | a0003c0003t0005g0218a0003c0003t0005g0219a0003c0003t0005g0221others(14): Show | 17 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(14): Show |
intron_variant | MODIFIER | c.510-8629G>A | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 2/5 | chr7 | 44436332 | ||||||
chr7:44436347
|
T | C | 17 | a0003c0003t0005g0218a0003c0003t0005g0219a0003c0003t0005g0221others(14): Show | 17 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(14): Show |
intron_variant | MODIFIER | c.510-8644A>G | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 2/5 | chr7 | 44436347 | ||||||
chr7:44436367
|
G | A | 7 | a0002c0002t0007g0196a0002c0002t0007g0197a0002c0002t0007g0198others(4): Show | 7 | HG00741.hp2 HG02486.hp2 HG02622.hp1 others(4): Show |
intron_variant | MODIFIER | c.510-8664C>T | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 2/5 | chr7 | 44436367 | ||||||
chr7:44436445
|
G | C | 1 | a0002c0002t0023g0209 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.510-8742C>G | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 2/5 | chr7 | 44436445 | ||||||
chr7:44436506
|
G | A | 17 | a0003c0003t0005g0218a0003c0003t0005g0219a0003c0003t0005g0221others(14): Show | 17 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(14): Show |
intron_variant | MODIFIER | c.510-8803C>T | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 2/5 | chr7 | 44436506 | ||||||
chr7:44436701
|
T | C | 1 | a0001c0001t0001g0114 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.510-8998A>G | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 2/5 | chr7 | 44436701 | ||||||
chr7:44436785
|
T | C | 2 | a0001c0001t0002g0058a0001c0001t0002g0178 | 2 | HG02602.hp2 HG04115.hp2 |
intron_variant | MODIFIER | c.510-9082A>G | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 2/5 | chr7 | 44436785 | ||||||
chr7:44436810
|
A | G | 1 | a0001c0001t0002g0047 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.510-9107T>C | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 2/5 | chr7 | 44436810 | ||||||
chr7:44436815
|
T | A | 2 | a0001c0001t0001g0126a0001c0001t0001g0128 | 2 | HG00642.hp2 HG01169.hp2 |
intron_variant | MODIFIER | c.510-9112A>T | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 2/5 | chr7 | 44436815 | ||||||
chr7:44436854
|
T | C | 5 | a0002c0002t0007g0196a0002c0002t0007g0197a0002c0002t0007g0198others(2): Show | 5 | HG02486.hp2 HG02622.hp1 HG03453.hp1 others(2): Show |
intron_variant | MODIFIER | c.510-9151A>G | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 2/5 | chr7 | 44436854 | ||||||
chr7:44436891
|
A | T | 2 | a0002c0002t0010g0193a0002c0002t0010g0201 | 2 | HG00741.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.510-9188T>A | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 2/5 | chr7 | 44436891 | ||||||
chr7:44437054
|
TTTTTC | T | 3 | a0002c0002t0008g0206a0002c0002t0011g0194a0002c0002t0011g0195 | 3 | HG02486.hp2 HG02622.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.510-9356_510-9352d others(7): Show |
NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 2/5 | chr7 | 44437054 | ||||||
chr7:44437069
|
C | CT | 23 | a0001c0001t0001g0021a0001c0001t0001g0100a0001c0001t0001g0130others(20): Show | 23 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(20): Show |
intron_variant | MODIFIER | c.510-9367dupA | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 2/5 | chr7 | 44437069 | ||||||
chr7:44437171
|
G | A | 1 | a0002c0002t0021g0217 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.510-9468C>T | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 2/5 | chr7 | 44437171 | ||||||
chr7:44437201
|
C | T | 1 | a0001c0001t0001g0006 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.510-9498G>A | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 2/5 | chr7 | 44437201 | ||||||
chr7:44437218
|
T | C | 17 | a0003c0003t0005g0218a0003c0003t0005g0219a0003c0003t0005g0221others(14): Show | 17 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(14): Show |
intron_variant | MODIFIER | c.510-9515A>G | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 2/5 | chr7 | 44437218 | ||||||
chr7:44437255
|
A | G | 11 | a0002c0002t0004g0207a0002c0002t0004g0208a0002c0002t0004g0210others(8): Show | 11 | HG00735.hp2 HG01070.hp2 HG01071.hp1 others(8): Show |
intron_variant | MODIFIER | c.510-9552T>C | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 2/5 | chr7 | 44437255 | ||||||
chr7:44437270
|
A | G | 2 | a0001c0001t0001g0050a0001c0001t0001g0109 | 2 | HG02145.hp2 NA18981.hp2 |
intron_variant | MODIFIER | c.510-9567T>C | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 2/5 | chr7 | 44437270 | ||||||
chr7:44437386
|
T | C | 1 | a0002c0002t0040g0237 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.510-9683A>G | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 2/5 | chr7 | 44437386 | ||||||
chr7:44437528
|
AGAG | A | 2 | a0002c0005t0012g0235a0002c0005t0012g0236 | 2 | HG02922.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.510-9828_510-9826d others(5): Show |
NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 2/5 | chr7 | 44437528 | ||||||
chr7:44437576
|
C | T | 2 | a0002c0002t0021g0217a0002c0002t0040g0237 | 2 | HG03486.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.510-9873G>A | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 2/5 | chr7 | 44437576 | ||||||
chr7:44438093
|
C | T | 1 | a0001c0001t0002g0058 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.510-10390G>A | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 2/5 | chr7 | 44438093 | ||||||
chr7:44438348
|
C | A | 1 | a0001c0001t0002g0099 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.510-10645G>T | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 2/5 | chr7 | 44438348 | ||||||
chr7:44438419
|
A | G | 19 | a0002c0002t0021g0217a0002c0002t0040g0237a0003c0003t0005g0218others(16): Show | 19 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(16): Show |
intron_variant | MODIFIER | c.510-10716T>C | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 2/5 | chr7 | 44438419 | ||||||
chr7:44438513
|
G | A | 19 | a0002c0002t0021g0217a0002c0002t0040g0237a0003c0003t0005g0218others(16): Show | 19 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(16): Show |
intron_variant | MODIFIER | c.510-10810C>T | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 2/5 | chr7 | 44438513 | ||||||
chr7:44438689
|
C | T | 1 | a0001c0001t0003g0135 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.510-10986G>A | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 2/5 | chr7 | 44438689 | ||||||
chr7:44438842
|
G | A | 1 | a0001c0001t0001g0155 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.510-11139C>T | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 2/5 | chr7 | 44438842 | ||||||
chr7:44438983
|
C | T | 17 | a0003c0003t0005g0218a0003c0003t0005g0219a0003c0003t0005g0221others(14): Show | 17 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(14): Show |
intron_variant | MODIFIER | c.510-11280G>A | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 2/5 | chr7 | 44438983 | ||||||
chr7:44439055
|
G | A | 2 | a0003c0003t0005g0218a0003c0003t0005g0219 | 2 | HG03491.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.510-11352C>T | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 2/5 | chr7 | 44439055 | ||||||
chr7:44439096
|
G | A | 1 | a0001c0001t0001g0119 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.510-11393C>T | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 2/5 | chr7 | 44439096 | ||||||
chr7:44439287
|
G | A | 19 | a0002c0002t0021g0217a0002c0002t0040g0237a0003c0003t0005g0218others(16): Show | 19 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(16): Show |
intron_variant | MODIFIER | c.510-11584C>T | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 2/5 | chr7 | 44439287 | ||||||
chr7:44439328
|
A | G | 1 | a0001c0001t0001g0105 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.510-11625T>C | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 2/5 | chr7 | 44439328 | ||||||
chr7:44439344
|
A | G | 2 | a0001c0001t0001g0156a0001c0001t0001g0158 | 2 | HG03834.hp1 NA20905.hp1 |
intron_variant | MODIFIER | c.510-11641T>C | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 2/5 | chr7 | 44439344 | ||||||
chr7:44439578
|
A | G | 19 | a0002c0002t0021g0217a0002c0002t0040g0237a0003c0003t0005g0218others(16): Show | 19 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(16): Show |
intron_variant | MODIFIER | c.510-11875T>C | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 2/5 | chr7 | 44439578 | ||||||
chr7:44439843
|
A | C | 1 | a0001c0001t0003g0043 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.510-12140T>G | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 2/5 | chr7 | 44439843 | ||||||
chr7:44439868
|
T | C | 5 | a0002c0002t0007g0196a0002c0002t0007g0197a0002c0002t0007g0198others(2): Show | 5 | HG02486.hp2 HG02622.hp1 HG03453.hp1 others(2): Show |
intron_variant | MODIFIER | c.510-12165A>G | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 2/5 | chr7 | 44439868 | ||||||
chr7:44439889
|
GCTAA | G | 19 | a0002c0002t0021g0217a0002c0002t0040g0237a0003c0003t0005g0218others(16): Show | 19 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(16): Show |
intron_variant | MODIFIER | c.510-12190_510-1218 others(8): Show |
NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 2/5 | chr7 | 44439889 | ||||||
chr7:44439935
|
A | G | 30 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(27): Show | 30 | HG00544.hp2 HG00639.hp1 HG02015.hp2 others(27): Show |
intron_variant | MODIFIER | c.510-12232T>C | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 2/5 | chr7 | 44439935 | ||||||
chr7:44440118
|
C | T | 1 | a0004c0004t0003g0016 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.510-12415G>A | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 2/5 | chr7 | 44440118 | ||||||
chr7:44440496
|
G | GA | 24 | a0001c0001t0001g0018a0001c0001t0001g0020a0001c0001t0001g0035others(21): Show | 24 | HG00438.hp2 HG00544.hp1 HG01070.hp1 others(21): Show |
intron_variant | MODIFIER | c.510-12794dupT | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 2/5 | chr7 | 44440496 | ||||||
chr7:44440496
|
G | GAAAAAAA others(1): Show |
8 | a0003c0003t0006g0226a0003c0003t0006g0229a0003c0003t0006g0231others(5): Show | 8 | HG00280.hp2 HG00438.hp1 HG02738.hp1 others(5): Show |
intron_variant | MODIFIER | c.510-12801_510-1279 others(12): Show |
NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 2/5 | chr7 | 44440496 | ||||||
chr7:44440496
|
G | GAAAAAAA others(2): Show |
6 | a0003c0003t0005g0219a0003c0003t0005g0221a0003c0003t0005g0224others(3): Show | 6 | HG00099.hp2 HG00280.hp1 HG01168.hp2 others(3): Show |
intron_variant | MODIFIER | c.510-12802_510-1279 others(13): Show |
NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 2/5 | chr7 | 44440496 | ||||||
chr7:44440496
|
G | GAAAAAAA others(3): Show |
2 | a0003c0003t0005g0218a0003c0003t0005g0222 | 2 | HG01256.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.510-12803_510-1279 others(14): Show |
NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 2/5 | chr7 | 44440496 | ||||||
chr7:44440496
|
G | GAAAAAAA others(4): Show |
1 | a0003c0003t0005g0223 | 1 | HG01258.hp2 | intron_variant | MODIFIER | c.510-12804_510-1279 others(15): Show |
NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 2/5 | chr7 | 44440496 | ||||||
chr7:44440496
|
GA | G | 12 | a0001c0001t0001g0046a0002c0002t0004g0207a0002c0002t0004g0208others(9): Show | 12 | HG00735.hp2 HG01070.hp2 HG01071.hp1 others(9): Show |
intron_variant | MODIFIER | c.510-12794delT | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 2/5 | chr7 | 44440496 | ||||||
chr7:44440549
|
AT | A | 19 | a0001c0001t0026g0186a0002c0002t0021g0217a0002c0002t0040g0237others(16): Show | 19 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(16): Show |
intron_variant | MODIFIER | c.510-12847delA | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 2/5 | chr7 | 44440549 | ||||||
chr7:44440594
|
A | G | 1 | a0001c0001t0002g0011 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.510-12891T>C | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 2/5 | chr7 | 44440594 | ||||||
chr7:44440596
|
A | G | 1 | a0001c0001t0001g0074 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.510-12893T>C | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 2/5 | chr7 | 44440596 | ||||||
chr7:44440688
|
T | C | 2 | a0001c0001t0001g0040a0001c0001t0001g0114 | 2 | NA18612.hp2 NA19074.hp2 |
intron_variant | MODIFIER | c.510-12985A>G | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 2/5 | chr7 | 44440688 | ||||||
chr7:44440865
|
C | T | 11 | a0002c0002t0004g0207a0002c0002t0004g0208a0002c0002t0004g0210others(8): Show | 11 | HG00735.hp2 HG01070.hp2 HG01071.hp1 others(8): Show |
intron_variant | MODIFIER | c.510-13162G>A | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 2/5 | chr7 | 44440865 | ||||||
chr7:44440888
|
T | C | 1 | a0002c0002t0023g0209 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.510-13185A>G | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 2/5 | chr7 | 44440888 | ||||||
chr7:44440951
|
A | G | 19 | a0002c0002t0021g0217a0002c0002t0040g0237a0003c0003t0005g0218others(16): Show | 19 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(16): Show |
intron_variant | MODIFIER | c.510-13248T>C | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 2/5 | chr7 | 44440951 | ||||||
chr7:44440954
|
C | A | 1 | a0001c0001t0026g0186 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.510-13251G>T | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 2/5 | chr7 | 44440954 | ||||||
chr7:44441081
|
G | A | 1 | a0002c0002t0040g0237 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.510-13378C>T | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 2/5 | chr7 | 44441081 | ||||||
chr7:44441091
|
A | G | 19 | a0002c0002t0021g0217a0002c0002t0040g0237a0003c0003t0005g0218others(16): Show | 19 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(16): Show |
intron_variant | MODIFIER | c.510-13388T>C | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 2/5 | chr7 | 44441091 | ||||||
chr7:44441244
|
A | T | 17 | a0003c0003t0005g0218a0003c0003t0005g0219a0003c0003t0005g0221others(14): Show | 17 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(14): Show |
intron_variant | MODIFIER | c.510-13541T>A | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 2/5 | chr7 | 44441244 | ||||||
chr7:44441545
|
T | C | 2 | a0001c0001t0001g0034a0001c0001t0003g0032 | 2 | NA18948.hp2 NA18971.hp2 |
intron_variant | MODIFIER | c.510-13842A>G | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 2/5 | chr7 | 44441545 | ||||||
chr7:44441554
|
G | A | 17 | a0003c0003t0005g0218a0003c0003t0005g0219a0003c0003t0005g0221others(14): Show | 17 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(14): Show |
intron_variant | MODIFIER | c.510-13851C>T | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 2/5 | chr7 | 44441554 | ||||||
chr7:44441673
|
C | T | 2 | a0001c0001t0002g0070a0001c0001t0002g0071 | 2 | HG02698.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.510-13970G>A | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 2/5 | chr7 | 44441673 | ||||||
chr7:44441674
|
G | A | 1 | a0001c0001t0001g0118 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.510-13971C>T | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 2/5 | chr7 | 44441674 | ||||||
chr7:44441768
|
G | A | 17 | a0003c0003t0005g0218a0003c0003t0005g0219a0003c0003t0005g0221others(14): Show | 17 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(14): Show |
intron_variant | MODIFIER | c.510-14065C>T | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 2/5 | chr7 | 44441768 | ||||||
chr7:44441907
|
C | T | 2 | a0002c0002t0010g0193a0002c0002t0010g0201 | 2 | HG00741.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.510-14204G>A | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 2/5 | chr7 | 44441907 | ||||||
chr7:44441937
|
C | T | 2 | a0002c0002t0010g0193a0002c0002t0010g0201 | 2 | HG00741.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.510-14234G>A | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 2/5 | chr7 | 44441937 | ||||||
chr7:44442025
|
C | T | 19 | a0002c0002t0021g0217a0002c0002t0040g0237a0003c0003t0005g0218others(16): Show | 19 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(16): Show |
intron_variant | MODIFIER | c.510-14322G>A | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 2/5 | chr7 | 44442025 | ||||||
chr7:44442038
|
A | G | 29 | a0002c0002t0007g0196a0002c0002t0007g0197a0002c0002t0007g0198others(26): Show | 29 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(26): Show |
intron_variant | MODIFIER | c.510-14335T>C | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 2/5 | chr7 | 44442038 | ||||||
chr7:44442111
|
C | T | 2 | a0003c0003t0019g0230a0003c0003t0019g0232 | 2 | HG00280.hp2 HG02738.hp1 |
intron_variant | MODIFIER | c.510-14408G>A | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 2/5 | chr7 | 44442111 | ||||||
chr7:44442389
|
A | T | 10 | a0001c0001t0001g0046a0001c0001t0001g0048a0001c0001t0001g0075others(7): Show | 10 | HG02109.hp2 HG02559.hp2 HG02622.hp2 others(7): Show |
intron_variant | MODIFIER | c.510-14686T>A | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 2/5 | chr7 | 44442389 | ||||||
chr7:44442693
|
C | CT | 47 | a0001c0001t0001g0005a0001c0001t0001g0010a0001c0001t0001g0012others(44): Show | 47 | HG00609.hp1 HG00609.hp2 HG00741.hp1 others(44): Show |
intron_variant | MODIFIER | c.510-14991dupA | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 2/5 | chr7 | 44442693 | ||||||
chr7:44442693
|
CT | C | 23 | a0001c0001t0001g0105a0001c0001t0001g0134a0001c0001t0002g0011others(20): Show | 23 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(20): Show |
intron_variant | MODIFIER | c.510-14991delA | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 2/5 | chr7 | 44442693 | ||||||
chr7:44442699
|
T | C | 1 | a0002c0002t0004g0207 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.510-14996A>G | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 2/5 | chr7 | 44442699 | ||||||
chr7:44442732
|
T | G | 2 | a0002c0002t0011g0194a0002c0002t0011g0195 | 2 | HG02486.hp2 HG02622.hp1 |
intron_variant | MODIFIER | c.510-15029A>C | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 2/5 | chr7 | 44442732 | ||||||
chr7:44442734
|
G | C | 2 | a0002c0002t0011g0194a0002c0002t0011g0195 | 2 | HG02486.hp2 HG02622.hp1 |
intron_variant | MODIFIER | c.510-15031C>G | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 2/5 | chr7 | 44442734 | ||||||
chr7:44442797
|
G | A | 2 | a0001c0001t0001g0048a0001c0001t0001g0140 | 2 | HG02922.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.510-15094C>T | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 2/5 | chr7 | 44442797 | ||||||
chr7:44443607
|
C | T | 2 | a0003c0003t0019g0230a0003c0003t0019g0232 | 2 | HG00280.hp2 HG02738.hp1 |
intron_variant | MODIFIER | c.510-15904G>A | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 2/5 | chr7 | 44443607 | ||||||
chr7:44443628
|
C | T | 2 | a0002c0002t0010g0193a0002c0002t0010g0201 | 2 | HG00741.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.510-15925G>A | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 2/5 | chr7 | 44443628 | ||||||
chr7:44443661
|
G | A | 13 | a0002c0002t0004g0207a0002c0002t0004g0208a0002c0002t0004g0210others(10): Show | 13 | HG00735.hp2 HG01070.hp2 HG01071.hp1 others(10): Show |
intron_variant | MODIFIER | c.510-15958C>T | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 2/5 | chr7 | 44443661 | ||||||
chr7:44443702
|
A | C | 29 | a0002c0002t0007g0196a0002c0002t0007g0197a0002c0002t0007g0198others(26): Show | 29 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(26): Show |
intron_variant | MODIFIER | c.510-15999T>G | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 2/5 | chr7 | 44443702 | ||||||
chr7:44443974
|
T | C | 2 | a0002c0002t0011g0194a0002c0002t0011g0195 | 2 | HG02486.hp2 HG02622.hp1 |
intron_variant | MODIFIER | c.510-16271A>G | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 2/5 | chr7 | 44443974 | ||||||
chr7:44444185
|
C | T | 17 | a0003c0003t0005g0218a0003c0003t0005g0219a0003c0003t0005g0221others(14): Show | 17 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(14): Show |
intron_variant | MODIFIER | c.510-16482G>A | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 2/5 | chr7 | 44444185 | ||||||
chr7:44444263
|
A | G | 1 | a0002c0002t0040g0237 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.510-16560T>C | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 2/5 | chr7 | 44444263 | ||||||
chr7:44444371
|
G | A | 14 | a0001c0001t0001g0040a0001c0001t0001g0049a0001c0001t0001g0093others(11): Show | 14 | HG00438.hp2 HG01496.hp1 HG01952.hp2 others(11): Show |
intron_variant | MODIFIER | c.510-16668C>T | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 2/5 | chr7 | 44444371 | ||||||
chr7:44444631
|
G | A | 19 | a0002c0002t0021g0217a0002c0002t0040g0237a0003c0003t0005g0218others(16): Show | 19 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(16): Show |
intron_variant | MODIFIER | c.510-16928C>T | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 2/5 | chr7 | 44444631 | ||||||
chr7:44444667
|
T | C | 5 | a0001c0001t0001g0017a0001c0001t0001g0018a0001c0001t0001g0019others(2): Show | 5 | HG02280.hp1 HG02615.hp1 HG02895.hp2 others(2): Show |
intron_variant | MODIFIER | c.510-16964A>G | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 2/5 | chr7 | 44444667 | ||||||
chr7:44444886
|
C | T | 1 | a0001c0001t0001g0163 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.510-17183G>A | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 2/5 | chr7 | 44444886 | ||||||
chr7:44444952
|
A | G | 19 | a0002c0002t0021g0217a0002c0002t0040g0237a0003c0003t0005g0218others(16): Show | 19 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(16): Show |
intron_variant | MODIFIER | c.510-17249T>C | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 2/5 | chr7 | 44444952 | ||||||
chr7:44445159
|
T | C | 19 | a0002c0002t0021g0217a0002c0002t0040g0237a0003c0003t0005g0218others(16): Show | 19 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(16): Show |
intron_variant | MODIFIER | c.510-17456A>G | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 2/5 | chr7 | 44445159 | ||||||
chr7:44445169
|
A | G | 2 | a0002c0002t0004g0213a0002c0002t0004g0216 | 2 | HG01070.hp2 HG01071.hp1 |
intron_variant | MODIFIER | c.510-17466T>C | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 2/5 | chr7 | 44445169 | ||||||
chr7:44445255
|
C | T | 1 | a0001c0001t0036g0144 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.510-17552G>A | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 2/5 | chr7 | 44445255 | ||||||
chr7:44445299
|
A | G | 2 | a0002c0002t0010g0193a0002c0002t0010g0201 | 2 | HG00741.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.510-17596T>C | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 2/5 | chr7 | 44445299 | ||||||
chr7:44445398
|
A | C | 1 | a0001c0001t0001g0116 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.510-17695T>G | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 2/5 | chr7 | 44445398 | ||||||
chr7:44445426
|
T | C | 1 | a0001c0001t0001g0035 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.510-17723A>G | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 2/5 | chr7 | 44445426 | ||||||
chr7:44445436
|
G | A | 1 | a0002c0002t0021g0217 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.510-17733C>T | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 2/5 | chr7 | 44445436 | ||||||
chr7:44445481
|
C | A | 234 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(231): Show | 235 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(232): Show |
intron_variant | MODIFIER | c.510-17778G>T | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 2/5 | chr7 | 44445481 | ||||||
chr7:44445750
|
G | C | 2 | a0002c0005t0012g0235a0002c0005t0012g0236 | 2 | HG02922.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.510-18047C>G | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 2/5 | chr7 | 44445750 | ||||||
chr7:44445992
|
T | C | 1 | a0002c0002t0040g0237 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.510-18289A>G | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 2/5 | chr7 | 44445992 | ||||||
chr7:44446106
|
C | T | 5 | a0001c0001t0001g0054a0001c0001t0001g0056a0001c0001t0001g0057others(2): Show | 5 | HG02257.hp2 HG02572.hp2 HG02723.hp1 others(2): Show |
intron_variant | MODIFIER | c.510-18403G>A | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 2/5 | chr7 | 44446106 | ||||||
chr7:44446692
|
C | T | 1 | a0001c0001t0001g0035 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.510-18989G>A | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 2/5 | chr7 | 44446692 | ||||||
chr7:44446955
|
T | C | 1 | a0001c0001t0001g0148 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.510-19252A>G | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 2/5 | chr7 | 44446955 | ||||||
chr7:44447139
|
A | C | 1 | a0001c0001t0001g0075 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.510-19436T>G | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 2/5 | chr7 | 44447139 | ||||||
chr7:44447199
|
G | A | 2 | a0002c0002t0004g0210a0002c0002t0004g0212 | 2 | HG00735.hp2 HG01106.hp1 |
intron_variant | MODIFIER | c.510-19496C>T | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 2/5 | chr7 | 44447199 | ||||||
chr7:44447281
|
C | T | 19 | a0002c0002t0021g0217a0002c0002t0040g0237a0003c0003t0005g0218others(16): Show | 19 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(16): Show |
intron_variant | MODIFIER | c.510-19578G>A | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 2/5 | chr7 | 44447281 | ||||||
chr7:44447322
|
G | A | 2 | a0002c0002t0004g0214a0002c0002t0022g0215 | 2 | HG01109.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.510-19619C>T | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 2/5 | chr7 | 44447322 | ||||||
chr7:44447345
|
C | T | 29 | a0002c0002t0007g0196a0002c0002t0007g0197a0002c0002t0007g0198others(26): Show | 29 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(26): Show |
intron_variant | MODIFIER | c.510-19642G>A | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 2/5 | chr7 | 44447345 | ||||||
chr7:44447414
|
A | T | 1 | a0002c0002t0040g0237 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.510-19711T>A | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 2/5 | chr7 | 44447414 | ||||||
chr7:44447490
|
G | T | 2 | a0001c0001t0001g0022a0001c0001t0001g0023 | 2 | NA18941.hp2 NA19003.hp2 |
intron_variant | MODIFIER | c.510-19787C>A | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 2/5 | chr7 | 44447490 | ||||||
chr7:44447778
|
A | G | 1 | a0001c0001t0001g0174 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.510-20075T>C | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 2/5 | chr7 | 44447778 | ||||||
chr7:44447931
|
T | C | 7 | a0002c0002t0007g0196a0002c0002t0007g0197a0002c0002t0007g0198others(4): Show | 7 | HG00741.hp2 HG02486.hp2 HG02622.hp1 others(4): Show |
intron_variant | MODIFIER | c.510-20228A>G | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 2/5 | chr7 | 44447931 | ||||||
chr7:44448287
|
T | C | 40 | a0002c0002t0004g0207a0002c0002t0004g0208a0002c0002t0004g0210others(37): Show | 40 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(37): Show |
intron_variant | MODIFIER | c.510-20584A>G | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 2/5 | chr7 | 44448287 | ||||||
chr7:44448288
|
G | A | 1 | a0002c0002t0040g0237 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.510-20585C>T | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 2/5 | chr7 | 44448288 | ||||||
chr7:44448288
|
G | T | 1 | a0001c0001t0002g0060 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.510-20585C>A | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 2/5 | chr7 | 44448288 | ||||||
chr7:44448502
|
G | A | 1 | a0003c0003t0005g0233 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.510-20799C>T | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 2/5 | chr7 | 44448502 | ||||||
chr7:44448701
|
C | T | 2 | a0002c0002t0020g0203a0002c0002t0038g0202 | 2 | HG02280.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.510-20998G>A | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 2/5 | chr7 | 44448701 | ||||||
chr7:44449049
|
A | G | 2 | a0002c0005t0012g0235a0002c0005t0012g0236 | 2 | HG02922.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.510-21346T>C | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 2/5 | chr7 | 44449049 | ||||||
chr7:44449088
|
C | T | 17 | a0003c0003t0005g0218a0003c0003t0005g0219a0003c0003t0005g0221others(14): Show | 17 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(14): Show |
intron_variant | MODIFIER | c.510-21385G>A | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 2/5 | chr7 | 44449088 | ||||||
chr7:44449240
|
G | A | 1 | a0001c0001t0001g0001 | 2 | HG01516.hp2 HG01517.hp2 |
intron_variant | MODIFIER | c.510-21537C>T | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 2/5 | chr7 | 44449240 | ||||||
chr7:44449578
|
G | A | 1 | a0002c0002t0021g0217 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.510-21875C>T | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 2/5 | chr7 | 44449578 | ||||||
chr7:44449852
|
TA | T | 35 | a0001c0001t0001g0017a0001c0001t0001g0018a0001c0001t0001g0019others(32): Show | 35 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(32): Show |
intron_variant | MODIFIER | c.510-22150delT | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 2/5 | chr7 | 44449852 | ||||||
chr7:44449922
|
T | C | 9 | a0001c0001t0001g0160a0001c0001t0001g0161a0001c0001t0001g0162others(6): Show | 9 | HG00741.hp1 HG01071.hp2 HG01168.hp1 others(6): Show |
intron_variant | MODIFIER | c.510-22219A>G | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 2/5 | chr7 | 44449922 | ||||||
chr7:44450061
|
C | A | 1 | a0001c0001t0001g0094 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.510-22358G>T | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 2/5 | chr7 | 44450061 | ||||||
chr7:44450175
|
T | C | 5 | a0001c0001t0001g0083a0001c0001t0001g0084a0001c0001t0001g0085others(2): Show | 5 | HG00735.hp1 HG01928.hp2 HG02683.hp1 others(2): Show |
intron_variant | MODIFIER | c.510-22472A>G | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 2/5 | chr7 | 44450175 | ||||||
chr7:44450179
|
A | AT | 12 | a0001c0001t0001g0074a0001c0001t0001g0179a0002c0002t0008g0205others(9): Show | 12 | HG00280.hp2 HG00438.hp1 HG01358.hp2 others(9): Show |
intron_variant | MODIFIER | c.510-22477dupA | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 2/5 | chr7 | 44450179 | ||||||
chr7:44450217
|
G | A | 17 | a0003c0003t0005g0218a0003c0003t0005g0219a0003c0003t0005g0221others(14): Show | 17 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(14): Show |
intron_variant | MODIFIER | c.510-22514C>T | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 2/5 | chr7 | 44450217 | ||||||
chr7:44450378
|
A | G | 3 | a0002c0002t0007g0196a0002c0002t0007g0197a0002c0002t0007g0198 | 3 | HG03453.hp1 HG03516.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.510-22675T>C | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 2/5 | chr7 | 44450378 | ||||||
chr7:44450422
|
C | T | 2 | a0001c0001t0001g0187a0001c0001t0001g0188 | 2 | HG01943.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.510-22719G>A | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 2/5 | chr7 | 44450422 | ||||||
chr7:44450467
|
T | C | 40 | a0002c0002t0004g0207a0002c0002t0004g0208a0002c0002t0004g0210others(37): Show | 40 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(37): Show |
intron_variant | MODIFIER | c.510-22764A>G | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 2/5 | chr7 | 44450467 | ||||||
chr7:44450468
|
G | A | 3 | a0002c0002t0021g0217a0002c0005t0012g0235a0002c0005t0012g0236 | 3 | HG02922.hp2 HG03486.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.510-22765C>T | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 2/5 | chr7 | 44450468 | ||||||
chr7:44450557
|
T | C | 1 | a0001c0001t0003g0135 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.510-22854A>G | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 2/5 | chr7 | 44450557 | ||||||
chr7:44450573
|
C | T | 1 | a0001c0001t0001g0165 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.510-22870G>A | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 2/5 | chr7 | 44450573 | ||||||
chr7:44450652
|
A | T | 17 | a0003c0003t0005g0218a0003c0003t0005g0219a0003c0003t0005g0221others(14): Show | 17 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(14): Show |
intron_variant | MODIFIER | c.510-22949T>A | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 2/5 | chr7 | 44450652 | ||||||
chr7:44450796
|
A | T | 8 | a0003c0003t0005g0218a0003c0003t0005g0219a0003c0003t0005g0221others(5): Show | 8 | HG00099.hp2 HG00280.hp1 HG01168.hp2 others(5): Show |
intron_variant | MODIFIER | c.510-23093T>A | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 2/5 | chr7 | 44450796 | ||||||
chr7:44451031
|
C | T | 1 | a0001c0001t0025g0129 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.510-23328G>A | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 2/5 | chr7 | 44451031 | ||||||
chr7:44451509
|
T | C | 3 | a0002c0002t0004g0207a0002c0002t0004g0208a0002c0002t0004g0211 | 3 | HG02683.hp2 HG03654.hp1 HG03942.hp1 |
intron_variant | MODIFIER | c.510-23806A>G | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 2/5 | chr7 | 44451509 | ||||||
chr7:44451571
|
G | A | 5 | a0001c0001t0001g0017a0001c0001t0001g0018a0001c0001t0001g0019others(2): Show | 5 | HG02280.hp1 HG02615.hp1 HG02895.hp2 others(2): Show |
intron_variant | MODIFIER | c.510-23868C>T | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 2/5 | chr7 | 44451571 | ||||||
chr7:44451604
|
G | A | 2 | a0003c0003t0005g0218a0003c0003t0005g0219 | 2 | HG03491.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.510-23901C>T | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 2/5 | chr7 | 44451604 | ||||||
chr7:44451668
|
T | G | 1 | a0002c0002t0021g0217 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.510-23965A>C | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 2/5 | chr7 | 44451668 | ||||||
chr7:44452036
|
G | C | 1 | a0001c0001t0001g0177 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.510-24333C>G | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 2/5 | chr7 | 44452036 | ||||||
chr7:44452041
|
G | A | 17 | a0003c0003t0005g0218a0003c0003t0005g0219a0003c0003t0005g0221others(14): Show | 17 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(14): Show |
intron_variant | MODIFIER | c.510-24338C>T | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 2/5 | chr7 | 44452041 | ||||||
chr7:44452058
|
T | G | 2 | a0003c0003t0005g0222a0003c0003t0005g0223 | 2 | HG01256.hp1 HG01258.hp2 |
intron_variant | MODIFIER | c.510-24355A>C | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 2/5 | chr7 | 44452058 | ||||||
chr7:44452264
|
G | A | 1 | a0001c0001t0003g0044 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.510-24561C>T | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 2/5 | chr7 | 44452264 | ||||||
chr7:44452454
|
C | T | 5 | a0001c0001t0001g0054a0001c0001t0001g0056a0001c0001t0001g0057others(2): Show | 5 | HG02257.hp2 HG02572.hp2 HG02723.hp1 others(2): Show |
intron_variant | MODIFIER | c.510-24751G>A | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 2/5 | chr7 | 44452454 | ||||||
chr7:44452699
|
T | C | 4 | a0001c0001t0001g0018a0001c0001t0001g0019a0001c0001t0001g0020others(1): Show | 4 | HG02280.hp1 HG02615.hp1 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.510-24996A>G | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 2/5 | chr7 | 44452699 | ||||||
chr7:44452729
|
G | C | 17 | a0003c0003t0005g0218a0003c0003t0005g0219a0003c0003t0005g0221others(14): Show | 17 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(14): Show |
intron_variant | MODIFIER | c.510-25026C>G | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 2/5 | chr7 | 44452729 | ||||||
chr7:44452824
|
A | C | 2 | a0002c0002t0010g0193a0002c0002t0010g0201 | 2 | HG00741.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.510-25121T>G | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 2/5 | chr7 | 44452824 | ||||||
chr7:44453029
|
T | C | 1 | a0001c0001t0001g0165 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.510-25326A>G | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 2/5 | chr7 | 44453029 | ||||||
chr7:44453075
|
G | A | 1 | a0002c0002t0023g0209 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.510-25372C>T | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 2/5 | chr7 | 44453075 | ||||||
chr7:44453081
|
G | A | 1 | a0001c0001t0001g0075 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.510-25378C>T | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 2/5 | chr7 | 44453081 | ||||||
chr7:44453168
|
C | T | 1 | a0001c0001t0002g0058 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.510-25465G>A | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 2/5 | chr7 | 44453168 | ||||||
chr7:44453233
|
A | C | 17 | a0003c0003t0005g0218a0003c0003t0005g0219a0003c0003t0005g0221others(14): Show | 17 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(14): Show |
intron_variant | MODIFIER | c.510-25530T>G | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 2/5 | chr7 | 44453233 | ||||||
chr7:44453349
|
T | C | 1 | a0002c0002t0040g0237 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.510-25646A>G | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 2/5 | chr7 | 44453349 | ||||||
chr7:44453360
|
T | A | 7 | a0002c0002t0007g0196a0002c0002t0007g0197a0002c0002t0007g0198others(4): Show | 7 | HG00741.hp2 HG02922.hp2 HG03139.hp1 others(4): Show |
intron_variant | MODIFIER | c.510-25657A>T | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 2/5 | chr7 | 44453360 | ||||||
chr7:44453406
|
A | G | 2 | a0001c0001t0001g0126a0001c0001t0001g0128 | 2 | HG00642.hp2 HG01169.hp2 |
intron_variant | MODIFIER | c.510-25703T>C | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 2/5 | chr7 | 44453406 | ||||||
chr7:44453770
|
G | C | 2 | a0002c0002t0021g0217a0002c0002t0040g0237 | 2 | HG03486.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.510-26067C>G | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 2/5 | chr7 | 44453770 | ||||||
chr7:44453813
|
G | A | 2 | a0002c0002t0021g0217a0002c0002t0040g0237 | 2 | HG03486.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.510-26110C>T | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 2/5 | chr7 | 44453813 | ||||||
chr7:44454164
|
G | A | 29 | a0002c0002t0007g0196a0002c0002t0007g0197a0002c0002t0007g0198others(26): Show | 29 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(26): Show |
intron_variant | MODIFIER | c.510-26461C>T | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 2/5 | chr7 | 44454164 | ||||||
chr7:44454271
|
G | A | 1 | a0001c0001t0002g0059 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.510-26568C>T | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 2/5 | chr7 | 44454271 | ||||||
chr7:44454317
|
T | C | 19 | a0002c0002t0021g0217a0002c0002t0040g0237a0003c0003t0005g0218others(16): Show | 19 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(16): Show |
intron_variant | MODIFIER | c.510-26614A>G | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 2/5 | chr7 | 44454317 | ||||||
chr7:44454651
|
G | A | 1 | a0001c0001t0014g0009 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.510-26948C>T | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 2/5 | chr7 | 44454651 | ||||||
chr7:44454772
|
A | T | 2 | a0002c0002t0018g0199a0002c0002t0018g0200 | 2 | HG02895.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.510-27069T>A | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 2/5 | chr7 | 44454772 | ||||||
chr7:44454773
|
T | A | 1 | a0002c0002t0023g0209 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.510-27070A>T | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 2/5 | chr7 | 44454773 | ||||||
chr7:44454847
|
T | C | 7 | a0002c0002t0007g0196a0002c0002t0007g0197a0002c0002t0007g0198others(4): Show | 7 | HG00741.hp2 HG02486.hp2 HG02622.hp1 others(4): Show |
intron_variant | MODIFIER | c.510-27144A>G | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 2/5 | chr7 | 44454847 | ||||||
chr7:44454936
|
A | AAC | 14 | a0001c0001t0001g0046a0001c0001t0001g0082a0001c0001t0001g0109others(11): Show | 14 | HG00642.hp2 HG01257.hp1 HG01496.hp1 others(11): Show |
intron_variant | MODIFIER | c.510-27235_510-2723 others(6): Show |
NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 2/5 | chr7 | 44454936 | ||||||
chr7:44454936
|
A | AACAC | 4 | a0002c0002t0007g0197a0002c0002t0007g0198a0002c0002t0010g0193others(1): Show | 4 | HG00741.hp2 HG03139.hp1 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.510-27237_510-2723 others(8): Show |
NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 2/5 | chr7 | 44454936 | ||||||
chr7:44454936
|
A | AACACAC | 3 | a0002c0002t0007g0196a0002c0005t0012g0235a0002c0005t0012g0236 | 3 | HG02922.hp2 HG03516.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.510-27239_510-2723 others(10): Show |
NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 2/5 | chr7 | 44454936 | ||||||
chr7:44454936
|
A | AC | 2 | a0001c0001t0002g0058a0001c0001t0016g0002 | 2 | HG00642.hp1 HG04115.hp2 |
intron_variant | MODIFIER | c.510-27234_510-2723 others(5): Show |
NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 2/5 | chr7 | 44454936 | ||||||
chr7:44454936
|
AAC | A | 14 | a0001c0001t0003g0043a0002c0002t0004g0207a0002c0002t0004g0208others(11): Show | 14 | HG00280.hp2 HG00438.hp1 HG01358.hp2 others(11): Show |
intron_variant | MODIFIER | c.510-27235_510-2723 others(6): Show |
NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 2/5 | chr7 | 44454936 | ||||||
chr7:44455216
|
T | C | 1 | a0002c0002t0040g0237 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.510-27513A>G | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 2/5 | chr7 | 44455216 | ||||||
chr7:44455294
|
C | T | 1 | a0001c0001t0001g0167 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.510-27591G>A | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 2/5 | chr7 | 44455294 | ||||||
chr7:44455333
|
G | A | 1 | a0001c0001t0033g0173 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.510-27630C>T | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 2/5 | chr7 | 44455333 | ||||||
chr7:44455345
|
A | G | 19 | a0002c0002t0021g0217a0002c0002t0040g0237a0003c0003t0005g0218others(16): Show | 19 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(16): Show |
intron_variant | MODIFIER | c.510-27642T>C | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 2/5 | chr7 | 44455345 | ||||||
chr7:44455690
|
A | G | 19 | a0002c0002t0021g0217a0002c0002t0040g0237a0003c0003t0005g0218others(16): Show | 19 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(16): Show |
intron_variant | MODIFIER | c.510-27987T>C | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 2/5 | chr7 | 44455690 | ||||||
chr7:44455941
|
G | T | 1 | a0002c0002t0021g0217 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.510-28238C>A | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 2/5 | chr7 | 44455941 | ||||||
chr7:44455983
|
G | A | 1 | a0002c0002t0022g0215 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.510-28280C>T | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 2/5 | chr7 | 44455983 | ||||||
chr7:44456000
|
T | TG | 19 | a0002c0002t0021g0217a0002c0002t0040g0237a0003c0003t0005g0218others(16): Show | 19 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(16): Show |
intron_variant | MODIFIER | c.510-28298dupC | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 2/5 | chr7 | 44456000 | ||||||
chr7:44456020
|
C | G | 5 | a0002c0002t0007g0196a0002c0002t0007g0197a0002c0002t0007g0198others(2): Show | 5 | HG02486.hp2 HG02622.hp1 HG03453.hp1 others(2): Show |
intron_variant | MODIFIER | c.510-28317G>C | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 2/5 | chr7 | 44456020 | ||||||
chr7:44456025
|
C | CA | 49 | a0001c0001t0001g0015a0001c0001t0001g0024a0001c0001t0001g0045others(46): Show | 49 | HG00438.hp2 HG00544.hp1 HG00544.hp2 others(46): Show |
intron_variant | MODIFIER | c.510-28323dupT | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 2/5 | chr7 | 44456025 | ||||||
chr7:44456025
|
C | CAA | 12 | a0001c0001t0001g0083a0001c0001t0001g0145a0002c0002t0004g0207others(9): Show | 12 | HG00741.hp2 HG01071.hp1 HG01106.hp1 others(9): Show |
intron_variant | MODIFIER | c.510-28324_510-2832 others(6): Show |
NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 2/5 | chr7 | 44456025 | ||||||
chr7:44456025
|
CAAAAAAA others(5): Show |
C | 5 | a0001c0001t0001g0046a0001c0001t0001g0048a0001c0001t0001g0075others(2): Show | 5 | HG02922.hp1 HG03041.hp2 HG03209.hp1 others(2): Show |
intron_variant | MODIFIER | c.510-28334_510-2832 others(16): Show |
NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 2/5 | chr7 | 44456025 | ||||||
chr7:44456036
|
A | C | 1 | a0001c0001t0001g0133 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.510-28333T>G | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 2/5 | chr7 | 44456036 | ||||||
chr7:44456037
|
A | C | 1 | a0001c0001t0002g0189 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.510-28334T>G | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 2/5 | chr7 | 44456037 | ||||||
chr7:44456038
|
AAAAAAAA others(6): Show |
A | 18 | a0002c0002t0021g0217a0002c0002t0040g0237a0003c0003t0005g0218others(15): Show | 18 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(15): Show |
intron_variant | MODIFIER | c.510-28348_510-2833 others(17): Show |
NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 2/5 | chr7 | 44456038 | ||||||
chr7:44456039
|
AAAAAAAA others(5): Show |
A | 1 | a0003c0003t0009g0228 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.510-28348_510-2833 others(16): Show |
NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 2/5 | chr7 | 44456039 | ||||||
chr7:44456041
|
A | C | 2 | a0002c0005t0012g0235a0002c0005t0012g0236 | 2 | HG02922.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.510-28338T>G | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 2/5 | chr7 | 44456041 | ||||||
chr7:44456051
|
C | A | 4 | a0001c0001t0001g0145a0002c0002t0007g0196a0002c0002t0007g0197others(1): Show | 4 | HG01106.hp2 HG03453.hp1 HG03516.hp1 others(1): Show |
intron_variant | MODIFIER | c.510-28348G>T | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 2/5 | chr7 | 44456051 | ||||||
chr7:44456063
|
C | CAACAAT | 17 | a0003c0003t0005g0218a0003c0003t0005g0219a0003c0003t0005g0221others(14): Show | 17 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(14): Show |
intron_variant | MODIFIER | c.510-28366_510-2836 others(10): Show |
NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 2/5 | chr7 | 44456063 | ||||||
chr7:44456136
|
C | G | 1 | a0001c0001t0001g0161 | 1 | HG01071.hp2 | intron_variant | MODIFIER | c.510-28433G>C | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 2/5 | chr7 | 44456136 | ||||||
chr7:44456164
|
C | T | 1 | a0001c0001t0001g0062 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.510-28461G>A | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 2/5 | chr7 | 44456164 | ||||||
chr7:44456352
|
T | C | 11 | a0002c0002t0004g0207a0002c0002t0004g0208a0002c0002t0004g0210others(8): Show | 11 | HG00735.hp2 HG01070.hp2 HG01071.hp1 others(8): Show |
intron_variant | MODIFIER | c.509+28616A>G | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 2/5 | chr7 | 44456352 | ||||||
chr7:44456406
|
T | A | 1 | a0002c0002t0021g0217 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.509+28562A>T | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 2/5 | chr7 | 44456406 | ||||||
chr7:44456564
|
T | C | 2 | a0002c0002t0010g0193a0002c0002t0010g0201 | 2 | HG00741.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.509+28404A>G | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 2/5 | chr7 | 44456564 | ||||||
chr7:44456608
|
T | C | 9 | a0003c0003t0006g0226a0003c0003t0006g0229a0003c0003t0006g0231others(6): Show | 9 | HG00280.hp2 HG00438.hp1 HG01358.hp2 others(6): Show |
intron_variant | MODIFIER | c.509+28360A>G | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 2/5 | chr7 | 44456608 | ||||||
chr7:44456650
|
G | A | 3 | a0001c0001t0001g0156a0001c0001t0001g0158a0001c0001t0001g0159 | 3 | HG03834.hp1 HG04204.hp2 NA20905.hp1 |
intron_variant | MODIFIER | c.509+28318C>T | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 2/5 | chr7 | 44456650 | ||||||
chr7:44456754
|
T | TA | 17 | a0002c0002t0021g0217a0002c0002t0040g0237a0003c0003t0005g0218others(14): Show | 17 | HG00099.hp2 HG00280.hp1 HG00438.hp1 others(14): Show |
intron_variant | MODIFIER | c.509+28213dupT | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 2/5 | chr7 | 44456754 | ||||||
chr7:44456969
|
T | C | 27 | a0002c0002t0007g0196a0002c0002t0007g0197a0002c0002t0007g0198others(24): Show | 27 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(24): Show |
intron_variant | MODIFIER | c.509+27999A>G | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 2/5 | chr7 | 44456969 | ||||||
chr7:44457027
|
T | TA | 11 | a0001c0001t0001g0036a0001c0001t0001g0037a0001c0001t0001g0038others(8): Show | 11 | HG00639.hp1 HG02109.hp1 HG02145.hp1 others(8): Show |
intron_variant | MODIFIER | c.509+27940dupT | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 2/5 | chr7 | 44457027 | ||||||
chr7:44457039
|
A | C | 1 | a0001c0001t0003g0043 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.509+27929T>G | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 2/5 | chr7 | 44457039 | ||||||
chr7:44457249
|
C | T | 27 | a0002c0002t0007g0196a0002c0002t0007g0197a0002c0002t0007g0198others(24): Show | 27 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(24): Show |
intron_variant | MODIFIER | c.509+27719G>A | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 2/5 | chr7 | 44457249 | ||||||
chr7:44457299
|
T | A | 19 | a0002c0002t0021g0217a0002c0002t0040g0237a0003c0003t0005g0218others(16): Show | 19 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(16): Show |
intron_variant | MODIFIER | c.509+27669A>T | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 2/5 | chr7 | 44457299 | ||||||
chr7:44457461
|
A | G | 1 | a0001c0001t0001g0109 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.509+27507T>C | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 2/5 | chr7 | 44457461 | ||||||
chr7:44457616
|
T | C | 2 | a0002c0002t0021g0217a0002c0002t0040g0237 | 2 | HG03486.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.509+27352A>G | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 2/5 | chr7 | 44457616 | ||||||
chr7:44457650
|
C | T | 29 | a0002c0002t0007g0196a0002c0002t0007g0197a0002c0002t0007g0198others(26): Show | 29 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(26): Show |
intron_variant | MODIFIER | c.509+27318G>A | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 2/5 | chr7 | 44457650 | ||||||
chr7:44457662
|
G | C | 29 | a0002c0002t0007g0196a0002c0002t0007g0197a0002c0002t0007g0198others(26): Show | 29 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(26): Show |
intron_variant | MODIFIER | c.509+27306C>G | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 2/5 | chr7 | 44457662 | ||||||
chr7:44457863
|
T | C | 2 | a0002c0002t0010g0193a0002c0002t0010g0201 | 2 | HG00741.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.509+27105A>G | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 2/5 | chr7 | 44457863 | ||||||
chr7:44458149
|
C | A | 3 | a0001c0001t0001g0156a0001c0001t0001g0158a0001c0001t0001g0159 | 3 | HG03834.hp1 HG04204.hp2 NA20905.hp1 |
intron_variant | MODIFIER | c.509+26819G>T | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 2/5 | chr7 | 44458149 | ||||||
chr7:44458476
|
A | G | 1 | a0002c0002t0040g0237 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.509+26492T>C | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 2/5 | chr7 | 44458476 | ||||||
chr7:44458619
|
T | C | 1 | a0002c0002t0040g0237 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.509+26349A>G | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 2/5 | chr7 | 44458619 | ||||||
chr7:44458659
|
G | A | 1 | a0001c0001t0002g0122 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.509+26309C>T | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 2/5 | chr7 | 44458659 | ||||||
chr7:44458663
|
G | GA | 44 | a0002c0002t0004g0207a0002c0002t0004g0208a0002c0002t0004g0210others(41): Show | 44 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(41): Show |
intron_variant | MODIFIER | c.509+26304dupT | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 2/5 | chr7 | 44458663 | ||||||
chr7:44458690
|
T | C | 1 | a0003c0003t0005g0233 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.509+26278A>G | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 2/5 | chr7 | 44458690 | ||||||
chr7:44458903
|
A | G | 9 | a0001c0001t0001g0036a0001c0001t0001g0037a0001c0001t0001g0038others(6): Show | 9 | HG00639.hp1 HG02109.hp1 HG02145.hp1 others(6): Show |
intron_variant | MODIFIER | c.509+26065T>C | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 2/5 | chr7 | 44458903 | ||||||
chr7:44458936
|
C | CTG | 29 | a0001c0001t0001g0008a0001c0001t0001g0034a0001c0001t0001g0039others(26): Show | 29 | HG00544.hp1 HG00642.hp1 HG01106.hp2 others(26): Show |
intron_variant | MODIFIER | c.509+26030_509+2603 others(6): Show |
NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 2/5 | chr7 | 44458936 | ||||||
chr7:44458936
|
C | CTGTG | 45 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0010others(42): Show | 45 | HG00099.hp1 HG00558.hp1 HG00558.hp2 others(42): Show |
intron_variant | MODIFIER | c.509+26028_509+2603 others(8): Show |
NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 2/5 | chr7 | 44458936 | ||||||
chr7:44458936
|
C | CTGTGTG | 32 | a0001c0001t0001g0007a0001c0001t0001g0012a0001c0001t0001g0028others(29): Show | 32 | HG00642.hp2 HG00741.hp1 HG01169.hp2 others(29): Show |
intron_variant | MODIFIER | c.509+26026_509+2603 others(10): Show |
NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 2/5 | chr7 | 44458936 | ||||||
chr7:44458936
|
C | CTGTGTGT others(1): Show |
24 | a0001c0001t0001g0024a0001c0001t0001g0048a0001c0001t0001g0051others(21): Show | 24 | HG01168.hp1 HG01169.hp1 HG01256.hp2 others(21): Show |
intron_variant | MODIFIER | c.509+26024_509+2603 others(12): Show |
NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 2/5 | chr7 | 44458936 | ||||||
chr7:44458936
|
C | CTGTGTGT others(3): Show |
14 | a0001c0001t0001g0021a0001c0001t0001g0057a0001c0001t0001g0086others(11): Show | 14 | HG00323.hp2 HG00438.hp2 HG00609.hp2 others(11): Show |
intron_variant | MODIFIER | c.509+26022_509+2603 others(14): Show |
NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 2/5 | chr7 | 44458936 | ||||||
chr7:44458936
|
C | CTGTGTGT others(5): Show |
7 | a0001c0001t0001g0056a0001c0001t0001g0080a0001c0001t0001g0085others(4): Show | 7 | HG00735.hp1 HG01175.hp2 HG02257.hp2 others(4): Show |
intron_variant | MODIFIER | c.509+26020_509+2603 others(16): Show |
NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 2/5 | chr7 | 44458936 | ||||||
chr7:44458936
|
C | CTGTGTGT others(7): Show |
2 | a0001c0001t0001g0083a0001c0001t0001g0134 | 2 | HG03041.hp1 HG03942.hp2 |
intron_variant | MODIFIER | c.509+26018_509+2603 others(18): Show |
NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 2/5 | chr7 | 44458936 | ||||||
chr7:44458936
|
C | CTGTGTGT others(9): Show |
1 | a0001c0001t0001g0054 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.509+26016_509+2603 others(20): Show |
NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 2/5 | chr7 | 44458936 | ||||||
chr7:44458936
|
CTG | C | 8 | a0001c0001t0001g0014a0001c0001t0001g0155a0001c0001t0002g0047others(5): Show | 8 | HG00639.hp2 HG01981.hp2 HG02109.hp2 others(5): Show |
intron_variant | MODIFIER | c.509+26030_509+2603 others(6): Show |
NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 2/5 | chr7 | 44458936 | ||||||
chr7:44458936
|
CTGTG | C | 9 | a0002c0002t0008g0205a0002c0002t0008g0206a0002c0002t0020g0203others(6): Show | 9 | HG00438.hp1 HG01358.hp2 HG04184.hp2 others(6): Show |
intron_variant | MODIFIER | c.509+26028_509+2603 others(8): Show |
NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 2/5 | chr7 | 44458936 | ||||||
chr7:44458936
|
CTGTGTG | C | 13 | a0001c0001t0001g0001a0001c0001t0001g0041a0001c0001t0003g0044others(10): Show | 14 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(11): Show |
intron_variant | MODIFIER | c.509+26026_509+2603 others(10): Show |
NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 2/5 | chr7 | 44458936 | ||||||
chr7:44458936
|
CTGTGTGT others(1): Show |
C | 3 | a0002c0002t0010g0193a0002c0002t0010g0201a0002c0002t0023g0209 | 3 | HG00741.hp2 HG03130.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.509+26024_509+2603 others(12): Show |
NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 2/5 | chr7 | 44458936 | ||||||
chr7:44458936
|
CTGTGTGT others(3): Show |
C | 2 | a0002c0002t0021g0217a0002c0002t0040g0237 | 2 | HG03486.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.509+26022_509+2603 others(14): Show |
NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 2/5 | chr7 | 44458936 | ||||||
chr7:44458936
|
CTGTGTGT others(7): Show |
C | 4 | a0002c0002t0004g0213a0002c0002t0004g0216a0002c0005t0012g0235others(1): Show | 4 | HG01070.hp2 HG01071.hp1 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.509+26018_509+2603 others(18): Show |
NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 2/5 | chr7 | 44458936 | ||||||
chr7:44458936
|
CTGTGTGT others(9): Show |
C | 5 | a0002c0002t0004g0207a0002c0002t0004g0208a0002c0002t0004g0211others(2): Show | 5 | HG01109.hp2 HG02683.hp2 HG02976.hp2 others(2): Show |
intron_variant | MODIFIER | c.509+26016_509+2603 others(20): Show |
NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 2/5 | chr7 | 44458936 | ||||||
chr7:44458936
|
CTGTGTGT others(13): Show |
C | 2 | a0002c0002t0004g0210a0002c0002t0004g0212 | 2 | HG00735.hp2 HG01106.hp1 |
intron_variant | MODIFIER | c.509+26012_509+2603 others(24): Show |
NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 2/5 | chr7 | 44458936 | ||||||
chr7:44459091
|
T | C | 17 | a0003c0003t0005g0218a0003c0003t0005g0219a0003c0003t0005g0221others(14): Show | 17 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(14): Show |
intron_variant | MODIFIER | c.509+25877A>G | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 2/5 | chr7 | 44459091 | ||||||
chr7:44459162
|
T | A | 1 | a0001c0001t0027g0146 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.509+25806A>T | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 2/5 | chr7 | 44459162 | ||||||
chr7:44459178
|
G | A | 7 | a0002c0002t0007g0196a0002c0002t0007g0197a0002c0002t0007g0198others(4): Show | 7 | HG00741.hp2 HG02486.hp2 HG02622.hp1 others(4): Show |
intron_variant | MODIFIER | c.509+25790C>T | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 2/5 | chr7 | 44459178 | ||||||
chr7:44459203
|
CT | C | 12 | a0001c0001t0001g0147a0002c0002t0004g0214a0002c0002t0007g0196others(9): Show | 12 | HG00741.hp2 HG02486.hp2 HG02622.hp1 others(9): Show |
intron_variant | MODIFIER | c.509+25764delA | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 2/5 | chr7 | 44459203 | ||||||
chr7:44459440
|
G | A | 2 | a0002c0005t0012g0235a0002c0005t0012g0236 | 2 | HG02922.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.509+25528C>T | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 2/5 | chr7 | 44459440 | ||||||
chr7:44459472
|
G | T | 1 | a0003c0003t0019g0232 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.509+25496C>A | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 2/5 | chr7 | 44459472 | ||||||
chr7:44459703
|
C | T | 1 | a0001c0001t0001g0105 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.509+25265G>A | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 2/5 | chr7 | 44459703 | ||||||
chr7:44460042
|
A | G | 1 | a0001c0001t0001g0116 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.509+24926T>C | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 2/5 | chr7 | 44460042 | ||||||
chr7:44460131
|
C | A | 7 | a0002c0002t0007g0196a0002c0002t0007g0197a0002c0002t0007g0198others(4): Show | 7 | HG00741.hp2 HG02486.hp2 HG02622.hp1 others(4): Show |
intron_variant | MODIFIER | c.509+24837G>T | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 2/5 | chr7 | 44460131 | ||||||
chr7:44460237
|
G | A | 3 | a0002c0002t0008g0204a0002c0002t0008g0205a0002c0002t0008g0206 | 3 | HG02257.hp1 NA18522.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.509+24731C>T | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 2/5 | chr7 | 44460237 | ||||||
chr7:44460722
|
A | G | 2 | a0001c0001t0001g0143a0001c0001t0001g0155 | 2 | NA18612.hp1 NA18960.hp2 |
intron_variant | MODIFIER | c.509+24246T>C | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 2/5 | chr7 | 44460722 | ||||||
chr7:44460803
|
T | C | 30 | a0001c0001t0001g0012a0001c0001t0001g0021a0001c0001t0001g0022others(27): Show | 30 | HG00609.hp1 HG01952.hp1 HG02015.hp1 others(27): Show |
intron_variant | MODIFIER | c.509+24165A>G | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 2/5 | chr7 | 44460803 | ||||||
chr7:44460821
|
T | C | 17 | a0003c0003t0005g0218a0003c0003t0005g0219a0003c0003t0005g0221others(14): Show | 17 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(14): Show |
intron_variant | MODIFIER | c.509+24147A>G | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 2/5 | chr7 | 44460821 | ||||||
chr7:44461026
|
C | T | 1 | a0002c0002t0040g0237 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.509+23942G>A | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 2/5 | chr7 | 44461026 | ||||||
chr7:44461056
|
C | T | 2 | a0002c0002t0018g0199a0002c0002t0018g0200 | 2 | HG02895.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.509+23912G>A | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 2/5 | chr7 | 44461056 | ||||||
chr7:44461274
|
T | C | 2 | a0001c0001t0001g0048a0001c0001t0001g0140 | 2 | HG02922.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.509+23694A>G | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 2/5 | chr7 | 44461274 | ||||||
chr7:44461406
|
G | A | 1 | a0002c0002t0021g0217 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.509+23562C>T | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 2/5 | chr7 | 44461406 | ||||||
chr7:44461525
|
G | C | 1 | a0001c0001t0030g0180 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.509+23443C>G | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 2/5 | chr7 | 44461525 | ||||||
chr7:44461670
|
T | A | 1 | a0002c0002t0021g0217 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.509+23298A>T | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 2/5 | chr7 | 44461670 | ||||||
chr7:44461748
|
C | T | 17 | a0003c0003t0005g0218a0003c0003t0005g0219a0003c0003t0005g0221others(14): Show | 17 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(14): Show |
intron_variant | MODIFIER | c.509+23220G>A | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 2/5 | chr7 | 44461748 | ||||||
chr7:44461790
|
G | T | 11 | a0002c0002t0004g0207a0002c0002t0004g0208a0002c0002t0004g0210others(8): Show | 11 | HG00735.hp2 HG01070.hp2 HG01071.hp1 others(8): Show |
intron_variant | MODIFIER | c.509+23178C>A | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 2/5 | chr7 | 44461790 | ||||||
chr7:44462067
|
A | C | 1 | a0001c0001t0034g0029 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.509+22901T>G | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 2/5 | chr7 | 44462067 | ||||||
chr7:44462141
|
G | A | 1 | a0001c0001t0001g0174 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.509+22827C>T | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 2/5 | chr7 | 44462141 | ||||||
chr7:44462170
|
T | C | 4 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(1): Show | 4 | HG02015.hp2 HG02071.hp1 NA18970.hp2 others(1): Show |
intron_variant | MODIFIER | c.509+22798A>G | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 2/5 | chr7 | 44462170 | ||||||
chr7:44462297
|
T | C | 2 | a0002c0002t0011g0194a0002c0002t0011g0195 | 2 | HG02486.hp2 HG02622.hp1 |
intron_variant | MODIFIER | c.509+22671A>G | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 2/5 | chr7 | 44462297 | ||||||
chr7:44462387
|
A | G | 3 | a0002c0002t0008g0204a0002c0002t0008g0205a0002c0002t0008g0206 | 3 | HG02257.hp1 NA18522.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.509+22581T>C | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 2/5 | chr7 | 44462387 | ||||||
chr7:44462521
|
C | T | 7 | a0002c0002t0007g0196a0002c0002t0007g0197a0002c0002t0007g0198others(4): Show | 7 | HG00741.hp2 HG02486.hp2 HG02622.hp1 others(4): Show |
intron_variant | MODIFIER | c.509+22447G>A | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 2/5 | chr7 | 44462521 | ||||||
chr7:44462587
|
C | T | 40 | a0002c0002t0004g0207a0002c0002t0004g0208a0002c0002t0004g0210others(37): Show | 40 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(37): Show |
intron_variant | MODIFIER | c.509+22381G>A | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 2/5 | chr7 | 44462587 | ||||||
chr7:44462678
|
T | A | 1 | a0001c0001t0027g0146 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.509+22290A>T | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 2/5 | chr7 | 44462678 | ||||||
chr7:44462816
|
A | G | 45 | a0002c0002t0004g0207a0002c0002t0004g0208a0002c0002t0004g0210others(42): Show | 45 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(42): Show |
intron_variant | MODIFIER | c.509+22152T>C | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 2/5 | chr7 | 44462816 | ||||||
chr7:44462864
|
T | C | 1 | a0001c0001t0001g0145 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.509+22104A>G | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 2/5 | chr7 | 44462864 | ||||||
chr7:44462866
|
T | A | 2 | a0002c0002t0021g0217a0002c0002t0040g0237 | 2 | HG03486.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.509+22102A>T | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 2/5 | chr7 | 44462866 | ||||||
chr7:44462945
|
C | CTG | 7 | a0001c0001t0001g0062a0001c0001t0001g0145a0001c0001t0002g0070others(4): Show | 7 | HG00639.hp2 HG01081.hp2 HG01106.hp2 others(4): Show |
intron_variant | MODIFIER | c.509+22021_509+2202 others(6): Show |
NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 2/5 | chr7 | 44462945 | ||||||
chr7:44462945
|
C | CTGTG | 6 | a0001c0001t0002g0059a0001c0001t0002g0060a0001c0001t0002g0061others(3): Show | 6 | HG00544.hp1 HG02071.hp2 HG02523.hp2 others(3): Show |
intron_variant | MODIFIER | c.509+22019_509+2202 others(8): Show |
NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 2/5 | chr7 | 44462945 | ||||||
chr7:44462945
|
C | CTGTGTG | 2 | a0001c0001t0002g0058a0001c0001t0002g0178 | 2 | HG02602.hp2 HG04115.hp2 |
intron_variant | MODIFIER | c.509+22017_509+2202 others(10): Show |
NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 2/5 | chr7 | 44462945 | ||||||
chr7:44462945
|
CTG | C | 17 | a0001c0001t0001g0017a0001c0001t0001g0046a0001c0001t0001g0131others(14): Show | 17 | HG00280.hp1 HG00438.hp1 HG00609.hp2 others(14): Show |
intron_variant | MODIFIER | c.509+22021_509+2202 others(6): Show |
NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 2/5 | chr7 | 44462945 | ||||||
chr7:44462945
|
CTGTG | C | 42 | a0001c0001t0001g0006a0001c0001t0001g0018a0001c0001t0001g0028others(39): Show | 42 | HG00323.hp1 HG00323.hp2 HG00438.hp2 others(39): Show |
intron_variant | MODIFIER | c.509+22019_509+2202 others(8): Show |
NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 2/5 | chr7 | 44462945 | ||||||
chr7:44462945
|
CTGTGTG | C | 121 | a0001c0001t0001g0005a0001c0001t0001g0007a0001c0001t0001g0008others(118): Show | 121 | HG00099.hp1 HG00099.hp2 HG00558.hp1 others(118): Show |
intron_variant | MODIFIER | c.509+22017_509+2202 others(10): Show |
NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 2/5 | chr7 | 44462945 | ||||||
chr7:44462945
|
CTGTGTGT others(1): Show |
C | 12 | a0001c0001t0001g0001a0001c0001t0001g0050a0001c0001t0001g0093others(9): Show | 13 | HG00673.hp2 HG00741.hp1 HG01109.hp2 others(10): Show |
intron_variant | MODIFIER | c.509+22015_509+2202 others(12): Show |
NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 2/5 | chr7 | 44462945 | ||||||
chr7:44462945
|
CTGTGTGT others(3): Show |
C | 4 | a0001c0001t0001g0119a0003c0003t0009g0220a0003c0003t0009g0227others(1): Show | 4 | HG01358.hp2 HG03471.hp2 HG04184.hp2 others(1): Show |
intron_variant | MODIFIER | c.509+22013_509+2202 others(14): Show |
NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 2/5 | chr7 | 44462945 | ||||||
chr7:44462953
|
G | C | 1 | a0001c0001t0001g0074 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.509+22015C>G | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 2/5 | chr7 | 44462953 | ||||||
chr7:44462979
|
GTGTGTGT others(5): Show |
G | 2 | a0002c0002t0010g0193a0002c0002t0010g0201 | 2 | HG00741.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.509+21977_509+2198 others(16): Show |
NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 2/5 | chr7 | 44462979 | ||||||
chr7:44462983
|
GTGTGTGT others(1): Show |
G | 2 | a0002c0002t0011g0194a0002c0002t0011g0195 | 2 | HG02486.hp2 HG02622.hp1 |
intron_variant | MODIFIER | c.509+21977_509+2198 others(12): Show |
NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 2/5 | chr7 | 44462983 | ||||||
chr7:44462985
|
GTGTGTA | G | 4 | a0001c0001t0001g0014a0001c0001t0001g0015a0001c0001t0001g0152others(1): Show | 4 | HG00544.hp2 HG02155.hp2 HG02602.hp1 others(1): Show |
intron_variant | MODIFIER | c.509+21977_509+2198 others(10): Show |
NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 2/5 | chr7 | 44462985 | ||||||
chr7:44462987
|
GTGTA | G | 2 | a0002c0002t0007g0196a0002c0002t0007g0197 | 2 | HG03453.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.509+21977_509+2198 others(8): Show |
NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 2/5 | chr7 | 44462987 | ||||||
chr7:44463026
|
G | C | 2 | a0002c0002t0007g0196a0002c0002t0007g0197 | 2 | HG03453.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.509+21942C>G | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 2/5 | chr7 | 44463026 | ||||||
chr7:44463172
|
A | T | 88 | a0001c0001t0001g0001a0001c0001t0001g0010a0001c0001t0001g0017others(85): Show | 89 | HG00099.hp1 HG00323.hp2 HG00438.hp2 others(86): Show |
intron_variant | MODIFIER | c.509+21796T>A | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 2/5 | chr7 | 44463172 | ||||||
chr7:44463213
|
A | G | 1 | a0002c0002t0004g0210 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.509+21755T>C | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 2/5 | chr7 | 44463213 | ||||||
chr7:44463336
|
G | T | 1 | a0001c0001t0001g0165 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.509+21632C>A | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 2/5 | chr7 | 44463336 | ||||||
chr7:44463356
|
C | T | 1 | a0001c0001t0030g0180 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.509+21612G>A | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 2/5 | chr7 | 44463356 | ||||||
chr7:44463472
|
G | C | 1 | a0001c0001t0003g0175 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.509+21496C>G | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 2/5 | chr7 | 44463472 | ||||||
chr7:44463605
|
C | G | 2 | a0002c0002t0004g0214a0002c0002t0022g0215 | 2 | HG01109.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.509+21363G>C | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 2/5 | chr7 | 44463605 | ||||||
chr7:44463855
|
T | C | 8 | a0001c0001t0001g0160a0001c0001t0001g0161a0001c0001t0001g0162others(5): Show | 8 | HG00741.hp1 HG01071.hp2 HG01168.hp1 others(5): Show |
intron_variant | MODIFIER | c.509+21113A>G | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 2/5 | chr7 | 44463855 | ||||||
chr7:44463957
|
T | C | 7 | a0002c0002t0007g0196a0002c0002t0007g0197a0002c0002t0007g0198others(4): Show | 7 | HG00741.hp2 HG02486.hp2 HG02622.hp1 others(4): Show |
intron_variant | MODIFIER | c.509+21011A>G | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 2/5 | chr7 | 44463957 | ||||||
chr7:44463970
|
T | C | 2 | a0002c0002t0021g0217a0002c0002t0040g0237 | 2 | HG03486.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.509+20998A>G | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 2/5 | chr7 | 44463970 | ||||||
chr7:44463987
|
G | A | 7 | a0002c0002t0007g0196a0002c0002t0007g0197a0002c0002t0007g0198others(4): Show | 7 | HG00741.hp2 HG02486.hp2 HG02622.hp1 others(4): Show |
intron_variant | MODIFIER | c.509+20981C>T | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 2/5 | chr7 | 44463987 | ||||||
chr7:44464077
|
G | A | 1 | a0001c0001t0001g0035 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.509+20891C>T | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 2/5 | chr7 | 44464077 | ||||||
chr7:44464213
|
C | CA | 8 | a0001c0001t0001g0038a0001c0001t0001g0045a0001c0001t0001g0046others(5): Show | 8 | HG01978.hp2 HG02109.hp1 HG02145.hp1 others(5): Show |
intron_variant | MODIFIER | c.509+20754dupT | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 2/5 | chr7 | 44464213 | ||||||
chr7:44464213
|
CA | C | 9 | a0001c0001t0002g0183a0002c0002t0007g0196a0002c0002t0007g0197others(6): Show | 9 | HG00741.hp2 HG01081.hp2 HG02486.hp2 others(6): Show |
intron_variant | MODIFIER | c.509+20754delT | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 2/5 | chr7 | 44464213 | ||||||
chr7:44464230
|
GA | G | 17 | a0003c0003t0005g0218a0003c0003t0005g0219a0003c0003t0005g0221others(14): Show | 17 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(14): Show |
intron_variant | MODIFIER | c.509+20737delT | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 2/5 | chr7 | 44464230 | ||||||
chr7:44464388
|
A | G | 2 | a0002c0002t0011g0194a0002c0002t0011g0195 | 2 | HG02486.hp2 HG02622.hp1 |
intron_variant | MODIFIER | c.509+20580T>C | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 2/5 | chr7 | 44464388 | ||||||
chr7:44464513
|
G | A | 17 | a0003c0003t0005g0218a0003c0003t0005g0219a0003c0003t0005g0221others(14): Show | 17 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(14): Show |
intron_variant | MODIFIER | c.509+20455C>T | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 2/5 | chr7 | 44464513 | ||||||
chr7:44464578
|
T | C | 26 | a0002c0002t0007g0196a0002c0002t0007g0197a0002c0002t0007g0198others(23): Show | 26 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(23): Show |
intron_variant | MODIFIER | c.509+20390A>G | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 2/5 | chr7 | 44464578 | ||||||
chr7:44464674
|
G | A | 1 | a0002c0002t0022g0215 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.509+20294C>T | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 2/5 | chr7 | 44464674 | ||||||
chr7:44465066
|
C | A | 1 | a0001c0001t0002g0052 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.509+19902G>T | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 2/5 | chr7 | 44465066 | ||||||
chr7:44465111
|
C | T | 86 | a0001c0001t0001g0001a0001c0001t0001g0010a0001c0001t0001g0017others(83): Show | 87 | HG00099.hp1 HG00323.hp2 HG00438.hp2 others(84): Show |
intron_variant | MODIFIER | c.509+19857G>A | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 2/5 | chr7 | 44465111 | ||||||
chr7:44465639
|
T | C | 2 | a0002c0005t0012g0235a0002c0005t0012g0236 | 2 | HG02922.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.509+19329A>G | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 2/5 | chr7 | 44465639 | ||||||
chr7:44465660
|
C | T | 2 | a0002c0002t0021g0217a0002c0002t0040g0237 | 2 | HG03486.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.509+19308G>A | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 2/5 | chr7 | 44465660 | ||||||
chr7:44465792
|
C | T | 1 | a0001c0001t0001g0174 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.509+19176G>A | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 2/5 | chr7 | 44465792 | ||||||
chr7:44465893
|
G | A | 1 | a0002c0002t0021g0217 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.509+19075C>T | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 2/5 | chr7 | 44465893 | ||||||
chr7:44466129
|
C | A | 2 | a0001c0001t0001g0038a0001c0001t0001g0045 | 2 | HG02109.hp1 HG02145.hp1 |
intron_variant | MODIFIER | c.509+18839G>T | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 2/5 | chr7 | 44466129 | ||||||
chr7:44466512
|
T | C | 1 | a0002c0002t0040g0237 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.509+18456A>G | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 2/5 | chr7 | 44466512 | ||||||
chr7:44466693
|
C | T | 1 | a0002c0002t0007g0198 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.509+18275G>A | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 2/5 | chr7 | 44466693 | ||||||
chr7:44466805
|
G | A | 1 | a0002c0002t0040g0237 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.509+18163C>T | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 2/5 | chr7 | 44466805 | ||||||
chr7:44466882
|
G | A | 1 | a0001c0001t0036g0144 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.509+18086C>T | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 2/5 | chr7 | 44466882 | ||||||
chr7:44467184
|
GAT | G | 2 | a0002c0002t0010g0193a0002c0002t0010g0201 | 2 | HG00741.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.509+17782_509+1778 others(6): Show |
NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 2/5 | chr7 | 44467184 | ||||||
chr7:44467394
|
C | T | 7 | a0002c0002t0004g0207a0002c0002t0004g0208a0002c0002t0004g0210others(4): Show | 7 | HG00735.hp2 HG01070.hp2 HG01071.hp1 others(4): Show |
intron_variant | MODIFIER | c.509+17574G>A | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 2/5 | chr7 | 44467394 | ||||||
chr7:44467543
|
G | A | 3 | a0002c0002t0008g0204a0002c0002t0008g0205a0002c0002t0008g0206 | 3 | HG02257.hp1 NA18522.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.509+17425C>T | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 2/5 | chr7 | 44467543 | ||||||
chr7:44467638
|
C | T | 1 | a0001c0001t0001g0100 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.509+17330G>A | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 2/5 | chr7 | 44467638 | ||||||
chr7:44467817
|
TA | T | 21 | a0001c0001t0001g0005a0001c0001t0001g0124a0002c0002t0021g0217others(18): Show | 21 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(18): Show |
intron_variant | MODIFIER | c.509+17150delT | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 2/5 | chr7 | 44467817 | ||||||
chr7:44467827
|
AAAAAG | A | 40 | a0001c0001t0001g0012a0001c0001t0001g0021a0001c0001t0001g0022others(37): Show | 40 | HG00609.hp1 HG00741.hp1 HG01071.hp2 others(37): Show |
intron_variant | MODIFIER | c.509+17136_509+1714 others(9): Show |
NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 2/5 | chr7 | 44467827 | ||||||
chr7:44467855
|
G | A | 2 | a0001c0001t0002g0011a0001c0001t0002g0047 | 2 | HG01981.hp2 HG03491.hp2 |
intron_variant | MODIFIER | c.509+17113C>T | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 2/5 | chr7 | 44467855 | ||||||
chr7:44467866
|
C | T | 3 | a0002c0002t0004g0207a0002c0002t0004g0208a0002c0002t0004g0211 | 3 | HG02683.hp2 HG03654.hp1 HG03942.hp1 |
intron_variant | MODIFIER | c.509+17102G>A | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 2/5 | chr7 | 44467866 | ||||||
chr7:44467867
|
G | A | 1 | a0002c0002t0040g0237 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.509+17101C>T | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 2/5 | chr7 | 44467867 | ||||||
chr7:44468033
|
G | A | 2 | a0001c0001t0002g0070a0001c0001t0002g0071 | 2 | HG02698.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.509+16935C>T | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 2/5 | chr7 | 44468033 | ||||||
chr7:44468079
|
G | A | 2 | a0002c0002t0004g0213a0002c0002t0004g0216 | 2 | HG01070.hp2 HG01071.hp1 |
intron_variant | MODIFIER | c.509+16889C>T | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 2/5 | chr7 | 44468079 | ||||||
chr7:44468284
|
C | T | 1 | a0002c0002t0023g0209 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.509+16684G>A | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 2/5 | chr7 | 44468284 | ||||||
chr7:44468285
|
G | A | 9 | a0002c0002t0004g0207a0002c0002t0004g0208a0002c0002t0004g0210others(6): Show | 9 | HG00735.hp2 HG01070.hp2 HG01071.hp1 others(6): Show |
intron_variant | MODIFIER | c.509+16683C>T | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 2/5 | chr7 | 44468285 | ||||||
chr7:44468289
|
C | T | 1 | a0001c0001t0001g0018 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.509+16679G>A | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 2/5 | chr7 | 44468289 | ||||||
chr7:44468349
|
C | CA | 37 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(34): Show | 37 | HG00544.hp2 HG00639.hp1 HG01175.hp2 others(34): Show |
intron_variant | MODIFIER | c.509+16618dupT | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 2/5 | chr7 | 44468349 | ||||||
chr7:44468349
|
CA | C | 13 | a0001c0001t0001g0018a0001c0001t0001g0019a0001c0001t0001g0102others(10): Show | 13 | HG00280.hp1 HG00323.hp1 HG01106.hp1 others(10): Show |
intron_variant | MODIFIER | c.509+16618delT | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 2/5 | chr7 | 44468349 | ||||||
chr7:44468349
|
CAA | C | 12 | a0002c0002t0007g0196a0002c0002t0007g0197a0002c0002t0007g0198others(9): Show | 12 | HG00099.hp2 HG00741.hp2 HG01168.hp2 others(9): Show |
intron_variant | MODIFIER | c.509+16617_509+1661 others(6): Show |
NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 2/5 | chr7 | 44468349 | ||||||
chr7:44468365
|
A | G | 2 | a0002c0002t0021g0217a0002c0002t0040g0237 | 2 | HG03486.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.509+16603T>C | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 2/5 | chr7 | 44468365 | ||||||
chr7:44468366
|
A | G | 10 | a0001c0001t0001g0142a0001c0001t0001g0147a0001c0001t0001g0148others(7): Show | 10 | HG02155.hp1 HG04184.hp1 NA18955.hp2 others(7): Show |
intron_variant | MODIFIER | c.509+16602T>C | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 2/5 | chr7 | 44468366 | ||||||
chr7:44468410
|
T | C | 1 | a0002c0002t0021g0217 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.509+16558A>G | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 2/5 | chr7 | 44468410 | ||||||
chr7:44468809
|
G | A | 1 | a0001c0001t0001g0101 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.509+16159C>T | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 2/5 | chr7 | 44468809 | ||||||
chr7:44469115
|
C | A | 1 | a0001c0001t0001g0179 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.509+15853G>T | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 2/5 | chr7 | 44469115 | ||||||
chr7:44469115
|
C | CA | 46 | a0001c0001t0001g0014a0001c0001t0001g0015a0001c0001t0001g0023others(43): Show | 46 | HG00323.hp2 HG00544.hp1 HG00544.hp2 others(43): Show |
intron_variant | MODIFIER | c.509+15852dupT | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 2/5 | chr7 | 44469115 | ||||||
chr7:44469115
|
C | CAA | 9 | a0001c0001t0001g0050a0001c0001t0001g0093a0001c0001t0001g0112others(6): Show | 9 | HG00438.hp2 HG00639.hp1 HG01106.hp2 others(6): Show |
intron_variant | MODIFIER | c.509+15851_509+1585 others(6): Show |
NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 2/5 | chr7 | 44469115 | ||||||
chr7:44469115
|
CA | C | 5 | a0001c0001t0001g0082a0001c0001t0001g0118a0001c0001t0001g0147others(2): Show | 5 | HG01081.hp2 HG03041.hp2 HG03130.hp1 others(2): Show |
intron_variant | MODIFIER | c.509+15852delT | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 2/5 | chr7 | 44469115 | ||||||
chr7:44469115
|
CAA | C | 9 | a0003c0003t0006g0226a0003c0003t0006g0229a0003c0003t0006g0231others(6): Show | 9 | HG00280.hp2 HG00438.hp1 HG01358.hp2 others(6): Show |
intron_variant | MODIFIER | c.509+15851_509+1585 others(6): Show |
NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 2/5 | chr7 | 44469115 | ||||||
chr7:44469115
|
CAAAA | C | 9 | a0002c0002t0004g0214a0002c0002t0022g0215a0003c0003t0005g0218others(6): Show | 9 | HG00099.hp2 HG00280.hp1 HG01109.hp2 others(6): Show |
intron_variant | MODIFIER | c.509+15849_509+1585 others(8): Show |
NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 2/5 | chr7 | 44469115 | ||||||
chr7:44469115
|
CAAAAAAA others(3): Show |
C | 1 | a0001c0001t0002g0052 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.509+15843_509+1585 others(14): Show |
NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 2/5 | chr7 | 44469115 | ||||||
chr7:44469193
|
T | A | 1 | a0003c0003t0019g0230 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.509+15775A>T | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 2/5 | chr7 | 44469193 | ||||||
chr7:44469224
|
G | A | 1 | a0001c0001t0001g0133 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.509+15744C>T | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 2/5 | chr7 | 44469224 | ||||||
chr7:44469438
|
G | A | 26 | a0002c0002t0007g0196a0002c0002t0007g0197a0002c0002t0007g0198others(23): Show | 26 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(23): Show |
intron_variant | MODIFIER | c.509+15530C>T | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 2/5 | chr7 | 44469438 | ||||||
chr7:44469520
|
T | C | 17 | a0003c0003t0005g0218a0003c0003t0005g0219a0003c0003t0005g0221others(14): Show | 17 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(14): Show |
intron_variant | MODIFIER | c.509+15448A>G | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 2/5 | chr7 | 44469520 | ||||||
chr7:44469525
|
G | C | 1 | a0001c0001t0001g0179 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.509+15443C>G | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 2/5 | chr7 | 44469525 | ||||||
chr7:44469531
|
G | A | 40 | a0002c0002t0004g0207a0002c0002t0004g0208a0002c0002t0004g0210others(37): Show | 40 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(37): Show |
intron_variant | MODIFIER | c.509+15437C>T | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 2/5 | chr7 | 44469531 | ||||||
chr7:44469702
|
A | C | 1 | a0001c0001t0001g0130 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.509+15266T>G | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 2/5 | chr7 | 44469702 | ||||||
chr7:44470100
|
G | T | 26 | a0002c0002t0007g0196a0002c0002t0007g0197a0002c0002t0007g0198others(23): Show | 26 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(23): Show |
intron_variant | MODIFIER | c.509+14868C>A | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 2/5 | chr7 | 44470100 | ||||||
chr7:44470110
|
T | C | 1 | a0002c0002t0004g0208 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.509+14858A>G | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 2/5 | chr7 | 44470110 | ||||||
chr7:44470117
|
G | A | 1 | a0002c0002t0040g0237 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.509+14851C>T | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 2/5 | chr7 | 44470117 | ||||||
chr7:44470144
|
T | C | 2 | a0002c0002t0018g0199a0002c0002t0018g0200 | 2 | HG02895.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.509+14824A>G | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 2/5 | chr7 | 44470144 | ||||||
chr7:44470204
|
T | A | 1 | a0002c0002t0007g0198 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.509+14764A>T | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 2/5 | chr7 | 44470204 | ||||||
chr7:44470425
|
C | T | 29 | a0002c0002t0007g0196a0002c0002t0007g0197a0002c0002t0007g0198others(26): Show | 29 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(26): Show |
intron_variant | MODIFIER | c.509+14543G>A | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 2/5 | chr7 | 44470425 | ||||||
chr7:44470476
|
A | G | 1 | a0001c0001t0027g0146 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.509+14492T>C | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 2/5 | chr7 | 44470476 | ||||||
chr7:44470477
|
T | A | 17 | a0003c0003t0005g0218a0003c0003t0005g0219a0003c0003t0005g0221others(14): Show | 17 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(14): Show |
intron_variant | MODIFIER | c.509+14491A>T | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 2/5 | chr7 | 44470477 | ||||||
chr7:44471238
|
G | A | 17 | a0003c0003t0005g0218a0003c0003t0005g0219a0003c0003t0005g0221others(14): Show | 17 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(14): Show |
intron_variant | MODIFIER | c.509+13730C>T | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 2/5 | chr7 | 44471238 | ||||||
chr7:44471612
|
A | C | 1 | a0001c0001t0029g0055 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.509+13356T>G | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 2/5 | chr7 | 44471612 | ||||||
chr7:44471737
|
C | T | 2 | a0002c0002t0021g0217a0002c0002t0040g0237 | 2 | HG03486.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.509+13231G>A | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 2/5 | chr7 | 44471737 | ||||||
chr7:44471862
|
C | T | 2 | a0002c0002t0010g0193a0002c0002t0010g0201 | 2 | HG00741.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.509+13106G>A | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 2/5 | chr7 | 44471862 | ||||||
chr7:44472046
|
C | A | 1 | a0001c0001t0001g0080 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.509+12922G>T | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 2/5 | chr7 | 44472046 | ||||||
chr7:44472046
|
C | T | 1 | a0001c0001t0037g0081 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.509+12922G>A | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 2/5 | chr7 | 44472046 | ||||||
chr7:44472556
|
A | G | 13 | a0001c0001t0001g0028a0001c0001t0001g0034a0001c0001t0001g0041others(10): Show | 13 | HG00323.hp2 HG01993.hp2 HG02165.hp1 others(10): Show |
intron_variant | MODIFIER | c.509+12412T>C | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 2/5 | chr7 | 44472556 | ||||||
chr7:44472644
|
C | T | 1 | a0002c0002t0040g0237 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.509+12324G>A | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 2/5 | chr7 | 44472644 | ||||||
chr7:44473154
|
C | T | 1 | a0001c0001t0001g0145 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.509+11814G>A | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 2/5 | chr7 | 44473154 | ||||||
chr7:44473157
|
A | G | 2 | a0002c0002t0018g0199a0002c0002t0018g0200 | 2 | HG02895.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.509+11811T>C | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 2/5 | chr7 | 44473157 | ||||||
chr7:44473392
|
A | C | 1 | a0001c0001t0001g0054 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.509+11576T>G | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 2/5 | chr7 | 44473392 | ||||||
chr7:44473535
|
T | C | 7 | a0002c0002t0007g0196a0002c0002t0007g0197a0002c0002t0007g0198others(4): Show | 7 | HG00741.hp2 HG02486.hp2 HG02622.hp1 others(4): Show |
intron_variant | MODIFIER | c.509+11433A>G | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 2/5 | chr7 | 44473535 | ||||||
chr7:44473749
|
A | G | 10 | a0001c0001t0001g0080a0002c0002t0004g0207a0002c0002t0004g0208others(7): Show | 10 | HG00735.hp2 HG01070.hp2 HG01071.hp1 others(7): Show |
intron_variant | MODIFIER | c.509+11219T>C | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 2/5 | chr7 | 44473749 | ||||||
chr7:44473845
|
A | G | 19 | a0002c0002t0021g0217a0002c0002t0040g0237a0003c0003t0005g0218others(16): Show | 19 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(16): Show |
intron_variant | MODIFIER | c.509+11123T>C | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 2/5 | chr7 | 44473845 | ||||||
chr7:44473959
|
C | G | 17 | a0003c0003t0005g0218a0003c0003t0005g0219a0003c0003t0005g0221others(14): Show | 17 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(14): Show |
intron_variant | MODIFIER | c.509+11009G>C | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 2/5 | chr7 | 44473959 | ||||||
chr7:44474083
|
G | C | 3 | a0002c0002t0007g0196a0002c0002t0007g0197a0002c0002t0007g0198 | 3 | HG03453.hp1 HG03516.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.509+10885C>G | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 2/5 | chr7 | 44474083 | ||||||
chr7:44474182
|
C | CA | 49 | a0001c0001t0001g0010a0001c0001t0001g0017a0001c0001t0001g0019others(46): Show | 49 | HG00438.hp2 HG00544.hp1 HG00558.hp1 others(46): Show |
intron_variant | MODIFIER | c.509+10785dupT | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 2/5 | chr7 | 44474182 | ||||||
chr7:44474182
|
CAA | C | 17 | a0003c0003t0005g0218a0003c0003t0005g0219a0003c0003t0005g0221others(14): Show | 17 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(14): Show |
intron_variant | MODIFIER | c.509+10784_509+1078 others(6): Show |
NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 2/5 | chr7 | 44474182 | ||||||
chr7:44474336
|
A | G | 3 | a0001c0001t0002g0052a0001c0001t0015g0053a0001c0001t0015g0079 | 3 | HG00323.hp1 HG01257.hp2 HG01258.hp1 |
intron_variant | MODIFIER | c.509+10632T>C | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 2/5 | chr7 | 44474336 | ||||||
chr7:44474387
|
A | G | 1 | a0002c0002t0040g0237 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.509+10581T>C | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 2/5 | chr7 | 44474387 | ||||||
chr7:44474413
|
T | C | 3 | a0002c0002t0007g0196a0002c0002t0007g0197a0002c0002t0007g0198 | 3 | HG03453.hp1 HG03516.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.509+10555A>G | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 2/5 | chr7 | 44474413 | ||||||
chr7:44474828
|
T | C | 2 | a0002c0002t0004g0214a0002c0002t0022g0215 | 2 | HG01109.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.509+10140A>G | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 2/5 | chr7 | 44474828 | ||||||
chr7:44474914
|
C | A | 1 | a0003c0003t0005g0225 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.509+10054G>T | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 2/5 | chr7 | 44474914 | ||||||
chr7:44474993
|
C | A | 1 | a0002c0002t0023g0209 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.509+9975G>T | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 2/5 | chr7 | 44474993 | ||||||
chr7:44475033
|
A | C | 1 | a0001c0001t0001g0036 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.509+9935T>G | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 2/5 | chr7 | 44475033 | ||||||
chr7:44475112
|
C | CT | 14 | a0001c0001t0001g0179a0001c0001t0001g0187a0001c0001t0002g0183others(11): Show | 14 | HG00280.hp2 HG00438.hp1 HG00639.hp2 others(11): Show |
intron_variant | MODIFIER | c.509+9855dupA | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 2/5 | chr7 | 44475112 | ||||||
chr7:44475112
|
C | CTT | 8 | a0003c0003t0005g0218a0003c0003t0005g0219a0003c0003t0005g0221others(5): Show | 8 | HG00099.hp2 HG00280.hp1 HG01168.hp2 others(5): Show |
intron_variant | MODIFIER | c.509+9854_509+9855d others(4): Show |
NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 2/5 | chr7 | 44475112 | ||||||
chr7:44475112
|
CT | C | 5 | a0001c0001t0001g0113a0001c0001t0001g0114a0001c0001t0003g0176others(2): Show | 5 | HG01070.hp1 HG01070.hp2 HG01257.hp2 others(2): Show |
intron_variant | MODIFIER | c.509+9855delA | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 2/5 | chr7 | 44475112 | ||||||
chr7:44475143
|
G | A | 2 | a0001c0001t0001g0141a0001c0001t0001g0167 | 2 | HG02015.hp1 HG02056.hp2 |
intron_variant | MODIFIER | c.509+9825C>T | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 2/5 | chr7 | 44475143 | ||||||
chr7:44475211
|
A | G | 5 | a0002c0002t0007g0196a0002c0002t0007g0197a0002c0002t0007g0198others(2): Show | 5 | HG02486.hp2 HG02622.hp1 HG03453.hp1 others(2): Show |
intron_variant | MODIFIER | c.509+9757T>C | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 2/5 | chr7 | 44475211 | ||||||
chr7:44475316
|
T | C | 8 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(5): Show | 8 | HG00544.hp2 HG02015.hp2 HG02071.hp1 others(5): Show |
intron_variant | MODIFIER | c.509+9652A>G | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 2/5 | chr7 | 44475316 | ||||||
chr7:44475668
|
G | C | 2 | a0002c0002t0011g0194a0002c0002t0011g0195 | 2 | HG02486.hp2 HG02622.hp1 |
intron_variant | MODIFIER | c.509+9300C>G | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 2/5 | chr7 | 44475668 | ||||||
chr7:44475717
|
A | G | 156 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(153): Show | 156 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(153): Show |
intron_variant | MODIFIER | c.509+9251T>C | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 2/5 | chr7 | 44475717 | ||||||
chr7:44476057
|
G | A | 1 | a0002c0002t0023g0209 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.509+8911C>T | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 2/5 | chr7 | 44476057 | ||||||
chr7:44476494
|
C | G | 1 | a0001c0001t0001g0017 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.509+8474G>C | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 2/5 | chr7 | 44476494 | ||||||
chr7:44476528
|
G | A | 1 | a0002c0002t0040g0237 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.509+8440C>T | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 2/5 | chr7 | 44476528 | ||||||
chr7:44476622
|
C | G | 8 | a0001c0001t0001g0036a0001c0001t0001g0037a0001c0001t0001g0038others(5): Show | 8 | HG00639.hp1 HG02109.hp1 HG02145.hp1 others(5): Show |
intron_variant | MODIFIER | c.509+8346G>C | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 2/5 | chr7 | 44476622 | ||||||
chr7:44476794
|
C | T | 2 | a0002c0002t0007g0196a0002c0002t0007g0197 | 2 | HG03453.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.509+8174G>A | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 2/5 | chr7 | 44476794 | ||||||
chr7:44476816
|
G | A | 1 | a0002c0002t0023g0209 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.509+8152C>T | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 2/5 | chr7 | 44476816 | ||||||
chr7:44476945
|
G | T | 3 | a0002c0002t0007g0196a0002c0002t0007g0197a0002c0002t0007g0198 | 3 | HG03453.hp1 HG03516.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.509+8023C>A | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 2/5 | chr7 | 44476945 | ||||||
chr7:44476954
|
C | CTGA | 3 | a0002c0002t0007g0196a0002c0002t0007g0197a0002c0002t0007g0198 | 3 | HG03453.hp1 HG03516.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.509+8011_509+8013d others(5): Show |
NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 2/5 | chr7 | 44476954 | ||||||
chr7:44477025
|
AT | A | 17 | a0003c0003t0005g0218a0003c0003t0005g0219a0003c0003t0005g0221others(14): Show | 17 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(14): Show |
intron_variant | MODIFIER | c.509+7942delA | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 2/5 | chr7 | 44477025 | ||||||
chr7:44477046
|
G | A | 1 | a0002c0002t0007g0198 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.509+7922C>T | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 2/5 | chr7 | 44477046 | ||||||
chr7:44477298
|
T | A | 7 | a0002c0002t0007g0196a0002c0002t0007g0197a0002c0002t0007g0198others(4): Show | 7 | HG00741.hp2 HG02486.hp2 HG02622.hp1 others(4): Show |
intron_variant | MODIFIER | c.509+7670A>T | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 2/5 | chr7 | 44477298 | ||||||
chr7:44477611
|
G | A | 17 | a0003c0003t0005g0218a0003c0003t0005g0219a0003c0003t0005g0221others(14): Show | 17 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(14): Show |
intron_variant | MODIFIER | c.509+7357C>T | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 2/5 | chr7 | 44477611 | ||||||
chr7:44477822
|
C | CT | 21 | a0001c0001t0001g0012a0001c0001t0001g0045a0001c0001t0001g0046others(18): Show | 21 | HG00323.hp2 HG00741.hp1 HG00741.hp2 others(18): Show |
intron_variant | MODIFIER | c.509+7145dupA | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 2/5 | chr7 | 44477822 | ||||||
chr7:44477822
|
CT | C | 28 | a0001c0001t0001g0134a0001c0001t0001g0168a0001c0001t0003g0043others(25): Show | 28 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(25): Show |
intron_variant | MODIFIER | c.509+7145delA | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 2/5 | chr7 | 44477822 | ||||||
chr7:44477830
|
T | C | 1 | a0001c0001t0001g0115 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.509+7138A>G | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 2/5 | chr7 | 44477830 | ||||||
chr7:44477895
|
A | G | 1 | a0001c0001t0003g0044 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.509+7073T>C | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 2/5 | chr7 | 44477895 | ||||||
chr7:44478098
|
T | C | 1 | a0002c0002t0021g0217 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.509+6870A>G | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 2/5 | chr7 | 44478098 | ||||||
chr7:44478115
|
T | A | 1 | a0001c0001t0001g0116 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.509+6853A>T | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 2/5 | chr7 | 44478115 | ||||||
chr7:44478231
|
C | G | 1 | a0001c0001t0001g0171 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.509+6737G>C | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 2/5 | chr7 | 44478231 | ||||||
chr7:44478247
|
A | G | 2 | a0002c0002t0021g0217a0002c0002t0040g0237 | 2 | HG03486.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.509+6721T>C | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 2/5 | chr7 | 44478247 | ||||||
chr7:44478300
|
C | T | 1 | a0002c0002t0021g0217 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.509+6668G>A | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 2/5 | chr7 | 44478300 | ||||||
chr7:44478454
|
A | G | 19 | a0002c0002t0021g0217a0002c0002t0040g0237a0003c0003t0005g0218others(16): Show | 19 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(16): Show |
intron_variant | MODIFIER | c.509+6514T>C | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 2/5 | chr7 | 44478454 | ||||||
chr7:44478467
|
C | T | 2 | a0003c0003t0005g0218a0003c0003t0005g0219 | 2 | HG03491.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.509+6501G>A | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 2/5 | chr7 | 44478467 | ||||||
chr7:44478714
|
A | G | 2 | a0002c0002t0010g0193a0002c0002t0010g0201 | 2 | HG00741.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.509+6254T>C | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 2/5 | chr7 | 44478714 | ||||||
chr7:44478781
|
A | G | 2 | a0002c0002t0021g0217a0002c0002t0040g0237 | 2 | HG03486.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.509+6187T>C | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 2/5 | chr7 | 44478781 | ||||||
chr7:44478945
|
T | C | 1 | a0002c0002t0040g0237 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.509+6023A>G | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 2/5 | chr7 | 44478945 | ||||||
chr7:44479049
|
C | A | 19 | a0002c0002t0021g0217a0002c0002t0040g0237a0003c0003t0005g0218others(16): Show | 19 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(16): Show |
intron_variant | MODIFIER | c.509+5919G>T | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 2/5 | chr7 | 44479049 | ||||||
chr7:44479086
|
G | A | 1 | a0001c0001t0001g0140 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.509+5882C>T | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 2/5 | chr7 | 44479086 | ||||||
chr7:44479334
|
C | T | 1 | a0001c0001t0001g0142 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.509+5634G>A | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 2/5 | chr7 | 44479334 | ||||||
chr7:44479472
|
A | T | 13 | a0001c0001t0001g0028a0001c0001t0001g0034a0001c0001t0001g0041others(10): Show | 13 | HG00323.hp2 HG01993.hp2 HG02165.hp1 others(10): Show |
intron_variant | MODIFIER | c.509+5496T>A | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 2/5 | chr7 | 44479472 | ||||||
chr7:44479477
|
A | G | 13 | a0001c0001t0001g0028a0001c0001t0001g0034a0001c0001t0001g0041others(10): Show | 13 | HG00323.hp2 HG01993.hp2 HG02165.hp1 others(10): Show |
intron_variant | MODIFIER | c.509+5491T>C | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 2/5 | chr7 | 44479477 | ||||||
chr7:44479538
|
T | C | 2 | a0002c0002t0021g0217a0002c0002t0040g0237 | 2 | HG03486.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.509+5430A>G | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 2/5 | chr7 | 44479538 | ||||||
chr7:44479650
|
G | A | 1 | a0002c0002t0040g0237 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.509+5318C>T | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 2/5 | chr7 | 44479650 | ||||||
chr7:44479670
|
T | G | 1 | a0001c0001t0001g0117 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.509+5298A>C | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 2/5 | chr7 | 44479670 | ||||||
chr7:44480024
|
G | A | 1 | a0002c0002t0040g0237 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.509+4944C>T | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 2/5 | chr7 | 44480024 | ||||||
chr7:44480635
|
A | C | 29 | a0002c0002t0007g0196a0002c0002t0007g0197a0002c0002t0007g0198others(26): Show | 29 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(26): Show |
intron_variant | MODIFIER | c.509+4333T>G | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 2/5 | chr7 | 44480635 | ||||||
chr7:44480659
|
T | A | 26 | a0002c0002t0007g0196a0002c0002t0007g0197a0002c0002t0007g0198others(23): Show | 26 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(23): Show |
intron_variant | MODIFIER | c.509+4309A>T | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 2/5 | chr7 | 44480659 | ||||||
chr7:44480712
|
C | T | 3 | a0002c0002t0008g0204a0002c0002t0008g0205a0002c0002t0008g0206 | 3 | HG02257.hp1 NA18522.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.509+4256G>A | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 2/5 | chr7 | 44480712 | ||||||
chr7:44480738
|
T | C | 2 | a0001c0001t0001g0169a0001c0001t0001g0170 | 2 | HG01168.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.509+4230A>G | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 2/5 | chr7 | 44480738 | ||||||
chr7:44480920
|
C | G | 3 | a0002c0002t0008g0204a0002c0002t0008g0205a0002c0002t0008g0206 | 3 | HG02257.hp1 NA18522.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.509+4048G>C | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 2/5 | chr7 | 44480920 | ||||||
chr7:44480941
|
C | CA | 40 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(37): Show | 40 | HG00438.hp2 HG00544.hp2 HG00642.hp2 others(37): Show |
intron_variant | MODIFIER | c.509+4026dupT | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 2/5 | chr7 | 44480941 | ||||||
chr7:44480941
|
C | CAAAAAAA others(8): Show |
1 | a0002c0002t0021g0217 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.509+4012_509+4026d others(17): Show |
NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 2/5 | chr7 | 44480941 | ||||||
chr7:44480941
|
C | CAAAAAAA others(10): Show |
1 | a0002c0002t0040g0237 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.509+4010_509+4026d others(19): Show |
NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 2/5 | chr7 | 44480941 | ||||||
chr7:44480941
|
CA | C | 12 | a0001c0001t0001g0036a0001c0001t0001g0037a0001c0001t0001g0038others(9): Show | 12 | HG00639.hp1 HG00741.hp2 HG01257.hp1 others(9): Show |
intron_variant | MODIFIER | c.509+4026delT | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 2/5 | chr7 | 44480941 | ||||||
chr7:44480941
|
CAAAA | C | 15 | a0003c0003t0005g0218a0003c0003t0005g0219a0003c0003t0005g0221others(12): Show | 15 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(12): Show |
intron_variant | MODIFIER | c.509+4023_509+4026d others(6): Show |
NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 2/5 | chr7 | 44480941 | ||||||
chr7:44480979
|
G | GA | 6 | a0001c0001t0001g0136a0001c0001t0001g0137a0001c0001t0001g0172others(3): Show | 6 | HG00323.hp2 HG00741.hp1 HG01109.hp1 others(3): Show |
intron_variant | MODIFIER | c.509+3988dupT | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 2/5 | chr7 | 44480979 | ||||||
chr7:44481256
|
A | C | 1 | a0001c0001t0001g0141 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.509+3712T>G | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 2/5 | chr7 | 44481256 | ||||||
chr7:44481412
|
T | A | 1 | a0002c0002t0021g0217 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.509+3556A>T | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 2/5 | chr7 | 44481412 | ||||||
chr7:44481578
|
A | G | 1 | a0002c0002t0020g0203 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.509+3390T>C | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 2/5 | chr7 | 44481578 | ||||||
chr7:44481602
|
C | T | 1 | a0001c0001t0001g0035 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.509+3366G>A | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 2/5 | chr7 | 44481602 | ||||||
chr7:44481921
|
A | G | 2 | a0002c0005t0012g0235a0002c0005t0012g0236 | 2 | HG02922.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.509+3047T>C | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 2/5 | chr7 | 44481921 | ||||||
chr7:44482222
|
G | C | 3 | a0002c0002t0007g0196a0002c0002t0007g0197a0002c0002t0007g0198 | 3 | HG03453.hp1 HG03516.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.509+2746C>G | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 2/5 | chr7 | 44482222 | ||||||
chr7:44482258
|
G | C | 2 | a0002c0002t0021g0217a0002c0002t0040g0237 | 2 | HG03486.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.509+2710C>G | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 2/5 | chr7 | 44482258 | ||||||
chr7:44482849
|
T | C | 1 | a0001c0001t0001g0139 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.509+2119A>G | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 2/5 | chr7 | 44482849 | ||||||
chr7:44483007
|
T | C | 1 | a0001c0001t0001g0140 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.509+1961A>G | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 2/5 | chr7 | 44483007 | ||||||
chr7:44483018
|
T | C | 19 | a0001c0001t0002g0183a0001c0001t0002g0184a0003c0003t0005g0218others(16): Show | 19 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(16): Show |
intron_variant | MODIFIER | c.509+1950A>G | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 2/5 | chr7 | 44483018 | ||||||
chr7:44483233
|
G | C | 3 | a0002c0002t0007g0196a0002c0002t0007g0197a0002c0002t0007g0198 | 3 | HG03453.hp1 HG03516.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.509+1735C>G | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 2/5 | chr7 | 44483233 | ||||||
chr7:44483475
|
C | T | 5 | a0002c0002t0007g0196a0002c0002t0007g0197a0002c0002t0007g0198others(2): Show | 5 | HG02486.hp2 HG02622.hp1 HG03453.hp1 others(2): Show |
intron_variant | MODIFIER | c.509+1493G>A | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 2/5 | chr7 | 44483475 | ||||||
chr7:44483670
|
C | T | 2 | a0002c0002t0007g0196a0002c0002t0007g0197 | 2 | HG03453.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.509+1298G>A | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 2/5 | chr7 | 44483670 | ||||||
chr7:44483876
|
T | G | 40 | a0001c0001t0001g0012a0001c0001t0001g0021a0001c0001t0001g0022others(37): Show | 40 | HG00609.hp1 HG00741.hp1 HG01071.hp2 others(37): Show |
intron_variant | MODIFIER | c.509+1092A>C | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 2/5 | chr7 | 44483876 | ||||||
chr7:44483914
|
G | A | 2 | a0002c0002t0018g0199a0002c0002t0018g0200 | 2 | HG02895.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.509+1054C>T | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 2/5 | chr7 | 44483914 | ||||||
chr7:44484052
|
C | G | 19 | a0002c0002t0021g0217a0002c0002t0040g0237a0003c0003t0005g0218others(16): Show | 19 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(16): Show |
intron_variant | MODIFIER | c.509+916G>C | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 2/5 | chr7 | 44484052 | ||||||
chr7:44484114
|
G | A | 1 | a0001c0001t0033g0173 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.509+854C>T | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 2/5 | chr7 | 44484114 | ||||||
chr7:44484518
|
A | G | 7 | a0001c0001t0001g0028a0001c0001t0001g0034a0001c0001t0003g0030others(4): Show | 7 | HG01993.hp2 HG02165.hp1 HG02293.hp1 others(4): Show |
intron_variant | MODIFIER | c.509+450T>C | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 2/5 | chr7 | 44484518 | ||||||
chr7:44484601
|
C | G | 21 | a0001c0001t0002g0183a0001c0001t0002g0184a0002c0002t0021g0217others(18): Show | 21 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(18): Show |
intron_variant | MODIFIER | c.509+367G>C | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 2/5 | chr7 | 44484601 | ||||||
chr7:44484754
|
C | G | 1 | a0002c0002t0040g0237 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.509+214G>C | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 2/5 | chr7 | 44484754 | ||||||
chr7:44484854
|
A | C | 1 | a0001c0001t0035g0027 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.509+114T>G | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 2/5 | chr7 | 44484854 | ||||||
chr7:44484939
|
G | A | 3 | a0002c0002t0007g0196a0002c0002t0007g0197a0002c0002t0007g0198 | 3 | HG03453.hp1 HG03516.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.509+29C>T | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 2/5 | chr7 | 44484939 | ||||||
chr7:44484952
|
A | C | 2 | a0002c0005t0012g0235a0002c0005t0012g0236 | 2 | HG02922.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.509+16T>G | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 2/5 | chr7 | 44484952 | ||||||
chr7:44485302
|
T | C | 1 | a0001c0001t0001g0174 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.193-18A>G | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 1/5 | chr7 | 44485302 | ||||||
chr7:44485589
|
T | C | 1 | a0003c0003t0005g0233 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.193-305A>G | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 1/5 | chr7 | 44485589 | ||||||
chr7:44485775
|
C | T | 28 | a0001c0001t0002g0183a0001c0001t0002g0184a0002c0002t0007g0196others(25): Show | 28 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(25): Show |
intron_variant | MODIFIER | c.193-491G>A | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 1/5 | chr7 | 44485775 | ||||||
chr7:44485798
|
G | A | 2 | a0002c0002t0021g0217a0002c0002t0040g0237 | 2 | HG03486.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.193-514C>T | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 1/5 | chr7 | 44485798 | ||||||
chr7:44485802
|
G | A | 2 | a0001c0001t0003g0175a0001c0001t0003g0176 | 2 | NA18974.hp1 NA19003.hp1 |
intron_variant | MODIFIER | c.193-518C>T | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 1/5 | chr7 | 44485802 | ||||||
chr7:44486034
|
C | T | 1 | a0001c0001t0001g0187 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.193-750G>A | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 1/5 | chr7 | 44486034 | ||||||
chr7:44486035
|
G | C | 1 | a0003c0003t0006g0234 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.193-751C>G | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 1/5 | chr7 | 44486035 | ||||||
chr7:44486091
|
G | A | 1 | a0001c0001t0001g0177 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.193-807C>T | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 1/5 | chr7 | 44486091 | ||||||
chr7:44486204
|
C | G | 21 | a0001c0001t0002g0183a0001c0001t0002g0184a0002c0002t0021g0217others(18): Show | 21 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(18): Show |
intron_variant | MODIFIER | c.193-920G>C | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 1/5 | chr7 | 44486204 | ||||||
chr7:44486508
|
T | C | 1 | a0001c0001t0002g0178 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.193-1224A>G | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 1/5 | chr7 | 44486508 | ||||||
chr7:44486521
|
GA | G | 11 | a0001c0001t0001g0017a0001c0001t0001g0018a0001c0001t0001g0019others(8): Show | 11 | HG01952.hp1 HG02280.hp1 HG02280.hp2 others(8): Show |
intron_variant | MODIFIER | c.193-1238delT | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 1/5 | chr7 | 44486521 | ||||||
chr7:44486766
|
G | T | 2 | a0001c0001t0001g0014a0001c0001t0001g0015 | 2 | HG00544.hp2 HG02155.hp2 |
intron_variant | MODIFIER | c.193-1482C>A | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 1/5 | chr7 | 44486766 | ||||||
chr7:44486839
|
C | T | 2 | a0002c0002t0010g0193a0002c0002t0010g0201 | 2 | HG00741.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.193-1555G>A | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 1/5 | chr7 | 44486839 | ||||||
chr7:44486857
|
C | G | 7 | a0002c0002t0007g0196a0002c0002t0007g0197a0002c0002t0007g0198others(4): Show | 7 | HG00741.hp2 HG02486.hp2 HG02622.hp1 others(4): Show |
intron_variant | MODIFIER | c.193-1573G>C | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 1/5 | chr7 | 44486857 | ||||||
chr7:44486876
|
T | C | 21 | a0001c0001t0002g0183a0001c0001t0002g0184a0002c0002t0021g0217others(18): Show | 21 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(18): Show |
intron_variant | MODIFIER | c.193-1592A>G | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 1/5 | chr7 | 44486876 | ||||||
chr7:44487331
|
G | A | 1 | a0002c0002t0007g0198 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.193-2047C>T | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 1/5 | chr7 | 44487331 | ||||||
chr7:44487460
|
G | GA | 23 | a0001c0001t0001g0179a0001c0001t0001g0181a0001c0001t0001g0182others(20): Show | 23 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(20): Show |
intron_variant | MODIFIER | c.193-2177dupT | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 1/5 | chr7 | 44487460 | ||||||
chr7:44487559
|
C | T | 2 | a0002c0002t0018g0199a0002c0002t0018g0200 | 2 | HG02895.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.193-2275G>A | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 1/5 | chr7 | 44487559 | ||||||
chr7:44487744
|
A | G | 2 | a0002c0002t0021g0217a0002c0002t0040g0237 | 2 | HG03486.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.193-2460T>C | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 1/5 | chr7 | 44487744 | ||||||
chr7:44487756
|
G | A | 1 | a0001c0001t0001g0185 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.193-2472C>T | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 1/5 | chr7 | 44487756 | ||||||
chr7:44487769
|
G | A | 1 | a0001c0001t0026g0186 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.193-2485C>T | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 1/5 | chr7 | 44487769 | ||||||
chr7:44487818
|
G | A | 1 | a0002c0002t0021g0217 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.193-2534C>T | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 1/5 | chr7 | 44487818 | ||||||
chr7:44487904
|
G | A | 2 | a0002c0005t0012g0235a0002c0005t0012g0236 | 2 | HG02922.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.192+2505C>T | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 1/5 | chr7 | 44487904 | ||||||
chr7:44487909
|
C | T | 1 | a0001c0001t0014g0013 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.192+2500G>A | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 1/5 | chr7 | 44487909 | ||||||
chr7:44488086
|
T | C | 234 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(231): Show | 235 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(232): Show |
intron_variant | MODIFIER | c.192+2323A>G | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 1/5 | chr7 | 44488086 | ||||||
chr7:44488318
|
G | A | 2 | a0002c0002t0021g0217a0002c0002t0040g0237 | 2 | HG03486.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.192+2091C>T | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 1/5 | chr7 | 44488318 | ||||||
chr7:44488333
|
T | C | 2 | a0001c0001t0001g0187a0001c0001t0001g0188 | 2 | HG01943.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.192+2076A>G | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 1/5 | chr7 | 44488333 | ||||||
chr7:44488338
|
GA | G | 8 | a0001c0001t0001g0012a0001c0001t0001g0191a0001c0001t0002g0011others(5): Show | 8 | HG02486.hp2 HG02622.hp1 HG03453.hp1 others(5): Show |
intron_variant | MODIFIER | c.192+2070delT | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 1/5 | chr7 | 44488338 | ||||||
chr7:44488338
|
GAA | G | 21 | a0002c0002t0010g0193a0002c0002t0010g0201a0002c0002t0021g0217others(18): Show | 21 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(18): Show |
intron_variant | MODIFIER | c.192+2069_192+2070d others(4): Show |
NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 1/5 | chr7 | 44488338 | ||||||
chr7:44488339
|
A | G | 1 | a0001c0001t0001g0010 | 1 | NA18975.hp1 | intron_variant | MODIFIER | c.192+2070T>C | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 1/5 | chr7 | 44488339 | ||||||
chr7:44488354
|
A | G | 7 | a0002c0002t0007g0196a0002c0002t0007g0197a0002c0002t0007g0198others(4): Show | 7 | HG00741.hp2 HG02486.hp2 HG02622.hp1 others(4): Show |
intron_variant | MODIFIER | c.192+2055T>C | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 1/5 | chr7 | 44488354 | ||||||
chr7:44488552
|
TC | T | 2 | a0002c0002t0018g0199a0002c0002t0018g0200 | 2 | HG02895.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.192+1856delG | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 1/5 | chr7 | 44488552 | ||||||
chr7:44488827
|
G | A | 17 | a0003c0003t0005g0218a0003c0003t0005g0219a0003c0003t0005g0221others(14): Show | 17 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(14): Show |
intron_variant | MODIFIER | c.192+1582C>T | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 1/5 | chr7 | 44488827 | ||||||
chr7:44488986
|
T | G | 1 | a0001c0001t0002g0189 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.192+1423A>C | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 1/5 | chr7 | 44488986 | ||||||
chr7:44489103
|
T | C | 1 | a0001c0001t0014g0009 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.192+1306A>G | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 1/5 | chr7 | 44489103 | ||||||
chr7:44489124
|
C | T | 2 | a0002c0002t0018g0199a0002c0002t0018g0200 | 2 | HG02895.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.192+1285G>A | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 1/5 | chr7 | 44489124 | ||||||
chr7:44489236
|
A | G | 1 | a0001c0001t0014g0009 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.192+1173T>C | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 1/5 | chr7 | 44489236 | ||||||
chr7:44489390
|
G | T | 4 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(1): Show | 4 | HG02015.hp2 HG02071.hp1 NA18970.hp2 others(1): Show |
intron_variant | MODIFIER | c.192+1019C>A | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 1/5 | chr7 | 44489390 | ||||||
chr7:44489660
|
T | C | 1 | a0002c0002t0021g0217 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.192+749A>G | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 1/5 | chr7 | 44489660 | ||||||
chr7:44489670
|
C | G | 5 | a0002c0002t0007g0196a0002c0002t0007g0197a0002c0002t0007g0198others(2): Show | 5 | HG02486.hp2 HG02622.hp1 HG03453.hp1 others(2): Show |
intron_variant | MODIFIER | c.192+739G>C | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 1/5 | chr7 | 44489670 | ||||||
chr7:44489675
|
A | T | 1 | a0002c0002t0040g0237 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.192+734T>A | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 1/5 | chr7 | 44489675 | ||||||
chr7:44489725
|
T | TGTAA | 234 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(231): Show | 235 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(232): Show |
intron_variant | MODIFIER | c.192+683_192+684ins others(4): Show |
NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 1/5 | chr7 | 44489725 | ||||||
chr7:44489799
|
T | C | 1 | a0001c0001t0002g0190 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.192+610A>G | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 1/5 | chr7 | 44489799 | ||||||
chr7:44489852
|
C | T | 1 | a0002c0002t0021g0217 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.192+557G>A | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 1/5 | chr7 | 44489852 | ||||||
chr7:44490063
|
G | A | 17 | a0003c0003t0005g0218a0003c0003t0005g0219a0003c0003t0005g0221others(14): Show | 17 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(14): Show |
intron_variant | MODIFIER | c.192+346C>T | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 1/5 | chr7 | 44490063 | ||||||
chr7:44490080
|
T | C | 1 | a0001c0001t0001g0191 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.192+329A>G | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 1/5 | chr7 | 44490080 | ||||||
chr7:44490127
|
G | A | 19 | a0002c0002t0021g0217a0002c0002t0040g0237a0003c0003t0005g0218others(16): Show | 19 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(16): Show |
intron_variant | MODIFIER | c.192+282C>T | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 1/5 | chr7 | 44490127 | ||||||
chr7:44490130
|
C | T | 1 | a0002c0002t0010g0193 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.192+279G>A | NUDCD3 | ENSG00000015676.18 | transcript | ENST00000355451.8 | protein_coding | 1/5 | chr7 | 44490130 |